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 2058 RMVar_ID_2058 Human_SNP_ID_659519068 A-to-I Human chr19 + 15115502 15115502 15115502 GCCCACCGCACATGCAGCCAGCCCAGGAGAGGAACACAAGCCCAGCTGGGACTGAAACAGCCTCC GCCCACCGCACATGCAGCCAGCCCAGGAGAGGGACACAAGCCCAGCTGGGACTGAAACAGCCTCC A G lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935576273 Functional Loss SNV dbSNP153 33..33 33 - - - 2059 RMVar_ID_2059 Human_SNP_ID_659570541 A-to-I Human chr19 - 15287804 15287802 15287804 GATCGTACCACTGCACTCCAGCTTGGGCGACAAAGGGAGACTGTCTCAAAAAAAAAAAAGAAATT GATCGTACCACTGCACTCCAGCTTGGGCGACA__GGGAGACTGTCTCAAAAAAAAAAAAGAAATT CTT C BRD4 Ensembl:ENSG00000141867 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1361984900 Functional Loss DEL dbSNP153 33..34 33 - - - 2060 RMVar_ID_2060 Human_SNP_ID_659570542 A-to-I Human chr19 - 15287804 15287804 15287804 GATCGTACCACTGCACTCCAGCTTGGGCGACAAAGGGAGACTGTCTCAAAAAAAAAAAAGAAATT GATCGTACCACTGCACTCCAGCTTGGGCGACAGAGGGAGACTGTCTCAAAAAAAAAAAAGAAATT T C BRD4 Ensembl:ENSG00000141867 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs902689385 Functional Loss SNV dbSNP153 33..33 33 - - - 2061 RMVar_ID_2061 Human_SNP_ID_659570557 A-to-I Human chr19 - 15287845 15287845 15287845 AGAATCGCCGAACCCAGGAGGTGGAGGTTGCAATGAGCCTAGATCGTACCACTGCACTCCAGCTT AGAATCGCCGAACCCAGGAGGTGGAGGTTGCAGTGAGCCTAGATCGTACCACTGCACTCCAGCTT T C BRD4 Ensembl:ENSG00000141867 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1012440686 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23309310 2062 RMVar_ID_2062 Human_SNP_ID_659570558 A-to-I Human chr19 - 15287846 15287846 15287846 AAGAATCGCCGAACCCAGGAGGTGGAGGTTGCAATGAGCCTAGATCGTACCACTGCACTCCAGCT AAGAATCGCCGAACCCAGGAGGTGGAGGTTGCGATGAGCCTAGATCGTACCACTGCACTCCAGCT T C BRD4 Ensembl:ENSG00000141867 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs969470505 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23309310 2063 RMVar_ID_2063 Human_SNP_ID_659578182 A-to-I Human chr19 - 15312685 15312685 15312685 GTGGTTCACCTACCTCAGCCTCCCAAAGTTCTAGGATTGCAGATGTGAGCCACCGTGCACAGCCT GTGGTTCACCTACCTCAGCCTCCCAAAGTTCTGGGATTGCAGATGTGAGCCACCGTGCACAGCCT T C BRD4 Ensembl:ENSG00000141867 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs550085574 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13381036 2064 RMVar_ID_2064 Human_SNP_ID_659583318 A-to-I Human chr19 - 15329037 15329037 15329037 CGGGCGTGGTGGCTCACGCCTGTGATCCCAGCACTTTGAGAGGCCGAGGCGGGCAGATCACCTGG CGGGCGTGGTGGCTCACGCCTGTGATCCCAGCGCTTTGAGAGGCCGAGGCGGGCAGATCACCTGG T C BRD4 Ensembl:ENSG00000141867 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs954815939 Functional Loss SNV dbSNP153 33..33 33 - - - 2065 RMVar_ID_2065 Human_SNP_ID_659585360 A-to-I Human chr19 + 15334719 15334719 15334719 GGCCAACATGGTGAAACTTCGACTCTACTAAAAATATAAAAATTAGCCAGGTATGGTAGCGGGTG GGCCAACATGGTGAAACTTCGACTCTACTAAAGATATAAAAATTAGCCAGGTATGGTAGCGGGTG A G lnc-OR7C2-1,lnc-CYP4F22-5,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008C26BB,RNACentral:URS00008BA3BC lincRNA,lincRNA,lincRNA intron,exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1346503125 Functional Loss SNV dbSNP153 33..33 33 - - - 2066 RMVar_ID_2066 Human_SNP_ID_659586236 A-to-I Human chr19 + 15338395 15338395 15338395 GTTGGCCCGACTGGTCTCAGAATCCTGGCCCTAAATGATCCGCCCACCTCCGCCTCCCAAAGTGT GTTGGCCCGACTGGTCTCAGAATCCTGGCCCTCAATGATCCGCCCACCTCCGCCTCCCAAAGTGT A C lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256513078 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25386847 RMVar_hsa_circ_193132 2067 RMVar_ID_2067 Human_SNP_ID_659586508 A-to-I Human chr19 + 15339560 15339560 15339560 AAACATCAGAAAGGTTGGGTGTGGTGGCTCACACCTGTAAAACCAGCACTTTGGGAGGCCGAGGA AAACATCAGAAAGGTTGGGTGTGGTGGCTCACGCCTGTAAAACCAGCACTTTGGGAGGCCGAGGA A G lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1166850618 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193132 2068 RMVar_ID_2068 Human_SNP_ID_659587756 A-to-I Human chr19 + 15344343 15344343 15344343 GGAGTAGCTGGGATTACCAAGTAGCTGGGATTACAGGCATGCGCTACCATGCCAGGGTAAGTTTT GGAGTAGCTGGGATTACCAAGTAGCTGGGATTGCAGGCATGCGCTACCATGCCAGGGTAAGTTTT A G lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1469362062 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193132 2069 RMVar_ID_2069 Human_SNP_ID_659587838 A-to-I Human chr19 + 15344728 15344728 15344728 TGGAGTGCAGTGGCGTGAACTTGGCTCACTGCAACCTCTGCCCCCCAGGTTCAAGCCATTCTCCT TGGAGTGCAGTGGCGTGAACTTGGCTCACTGCCACCTCTGCCCCCCAGGTTCAAGCCATTCTCCT A C lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs923844146 Functional Loss SNV dbSNP153 33..33 33 - - - 2070 RMVar_ID_2070 Human_SNP_ID_659587853 A-to-I Human chr19 + 15344788 15344787 15344788 CTCCTGCCTCAGCTTCCTGAATAGCTGGGATTACAGGCATGTGCCACAACACCTGGCTAATTTTG CTCCTGCCTCAGCTTCCTGAATAGCTGGGATT_CAGGCATGTGCCACAACACCTGGCTAATTTTG TA T lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs542984952 Functional Loss DEL dbSNP153 33..33 33 - - - 2071 RMVar_ID_2071 Human_SNP_ID_659588042 A-to-I Human chr19 + 15345663 15345663 15345663 TATGCTTTAAACACAGGCTCGCGGTGGCTCACACCTGAAATTCCAGCACTTCCGGAAGCTGAGGC TATGCTTTAAACACAGGCTCGCGGTGGCTCACGCCTGAAATTCCAGCACTTCCGGAAGCTGAGGC A G lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1344499962 Functional Loss SNV dbSNP153 33..33 33 - - - 2072 RMVar_ID_2072 Human_SNP_ID_659588739 A-to-I Human chr19 + 15348246 15348246 15348246 CGAGACCATCCTTGCCAACATGGCGAAACCCCATCTCTACTAAAAATACAAAAATCAGCTGGGTG CGAGACCATCCTTGCCAACATGGCGAAACCCCGTCTCTACTAAAAATACAAAAATCAGCTGGGTG A G lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1000759768 Functional Loss SNV dbSNP153 33..33 33 - - - 2073 RMVar_ID_2073 Human_SNP_ID_659589157 A-to-I Human chr19 + 15349628 15349628 15349628 TCACCCAGGCTAAAGTGCAGTGGCACGATCTCAGCTCACTGGAACCTCTGCCTCCCAGTTCAAGC TCACCCAGGCTAAAGTGCAGTGGCACGATCTCTGCTCACTGGAACCTCTGCCTCCCAGTTCAAGC A T lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1207859939 Functional Loss SNV dbSNP153 33..33 33 - - - 2074 RMVar_ID_2074 Human_SNP_ID_659590116 A-to-I Human chr19 + 15352947 15352947 15352947 TGGAGTGCAGTAGCGCAACCTCGACTCACTGCAGCCTCTGCCTCCCTGGTTCAAGCGATTCTTCT TGGAGTGCAGTAGCGCAACCTCGACTCACTGCGGCCTCTGCCTCCCTGGTTCAAGCGATTCTTCT A G lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs938296684 Functional Loss SNV dbSNP153 33..33 33 - - - 2075 RMVar_ID_2075 Human_SNP_ID_659590117 A-to-I Human chr19 + 15352947 15352947 15352947 TGGAGTGCAGTAGCGCAACCTCGACTCACTGCAGCCTCTGCCTCCCTGGTTCAAGCGATTCTTCT TGGAGTGCAGTAGCGCAACCTCGACTCACTGCTGCCTCTGCCTCCCTGGTTCAAGCGATTCTTCT A T lnc-OR7C2-1,lnc-OR7C2-1:2 RNACentral:URS00008BA729,RNACentral:URS00008BA3BC lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs938296684 Functional Loss SNV dbSNP153 33..33 33 - - - 2076 RMVar_ID_2076 Human_SNP_ID_659591169 A-to-I Human chr19 - 15355940 15355940 15355940 CCTGAGGTCTGGAGTTCCAGACCAGTCTGCCCAACATGGTGAAACCCCGTCTCCACTAAAAATAC CCTGAGGTCTGGAGTTCCAGACCAGTCTGCCCCACATGGTGAAACCCCGTCTCCACTAAAAATAC T G AKAP8 Ensembl:ENSG00000105127 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1198724379 Functional Loss SNV dbSNP153 33..33 33 - - - 2077 RMVar_ID_2077 Human_SNP_ID_659591185 A-to-I Human chr19 - 15355986 15355986 15355986 CGTGCCTGTAATCCCAGCATTTTGGGAGGCCAAGGCAGGCGGATCACCTGAGGTCTGGAGTTCCA CGTGCCTGTAATCCCAGCATTTTGGGAGGCCACGGCAGGCGGATCACCTGAGGTCTGGAGTTCCA T G AKAP8 Ensembl:ENSG00000105127 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1030911966 Functional Loss SNV dbSNP153 33..33 33 - - - 2078 RMVar_ID_2078 Human_SNP_ID_659591572 A-to-I Human chr19 - 15357307 15357307 15357307 CTCCTGCCTCAGCCTCCTGAGTACCTGGGACTACAGGCGCCCACCACCATGCCTGGCTAATGTTT CTCCTGCCTCAGCCTCCTGAGTACCTGGGACTGCAGGCGCCCACCACCATGCCTGGCTAATGTTT T C AKAP8 Ensembl:ENSG00000105127 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1448251242 Functional Loss SNV dbSNP153 33..33 33 - - - 2079 RMVar_ID_2079 Human_SNP_ID_659591916 A-to-I Human chr19 - 15358485 15358485 15358485 GCGGGGAACCGGGAATTATGGCTCATGCCTGTAATGCCAATAGTTTGGGAGGCTGAGGCAGGAGG GCGGGGAACCGGGAATTATGGCTCATGCCTGTGATGCCAATAGTTTGGGAGGCTGAGGCAGGAGG T C AKAP8 Ensembl:ENSG00000105127 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1483065296 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6723902 2080 RMVar_ID_2080 Human_SNP_ID_659594534 A-to-I Human chr19 - 15365831 15365822 15365831 TTTAGTAGTGACGGGGTTTCACCATGTTGGCCAGACTGGTCTCAAACTCCTGACCTCAGGTGATC TTTAGTAGTGACGGGGTTTCACCATGTTGGCC_________TCAAACTCCTGACCTCAGGTGATC AGACCAGTCT A AKAP8 Ensembl:ENSG00000105127 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1342687521 Functional Loss DEL dbSNP153 33..41 33 - - - RMVar_hsa_circ_33045,RMVar_hsa_circ_355440,RMVar_hsa_circ_52196,RMVar_hsa_circ_193135,RMVar_hsa_circ_52081,RMVar_hsa_circ_58942 2081 RMVar_ID_2081 Human_SNP_ID_659594552 A-to-I Human chr19 - 15365901 15365901 15365901 CTCCTACCTCCGCCTCCCAAGTAGCTGGAATTACAGGCGCCCGCCACCACACCCAGCTAATTTTT CTCCTACCTCCGCCTCCCAAGTAGCTGGAATTGCAGGCGCCCGCCACCACACCCAGCTAATTTTT T C AKAP8 Ensembl:ENSG00000105127 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs889990164 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33045,RMVar_hsa_circ_355440,RMVar_hsa_circ_52196,RMVar_hsa_circ_193135,RMVar_hsa_circ_52081,RMVar_hsa_circ_58942 2082 RMVar_ID_2082 Human_SNP_ID_659595120 A-to-I Human chr19 - 15367489 15367489 15367489 GAGTCTTGCTCTGTCGCCCAGGCTGGAGTGCAATAGCATAATCTCGGCTCACTATAACCTCTGCC GAGTCTTGCTCTGTCGCCCAGGCTGGAGTGCAGTAGCATAATCTCGGCTCACTATAACCTCTGCC T C AKAP8 Ensembl:ENSG00000105127 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1004233555 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33045,RMVar_hsa_circ_355440,RMVar_hsa_circ_52196,RMVar_hsa_circ_193135,RMVar_hsa_circ_52081,RMVar_hsa_circ_58942 2083 RMVar_ID_2083 Human_SNP_ID_659598148 A-to-I Human chr19 - 15376210 15376210 15376210 CCTCATTAGTAAGATCTTTCATTAGCTGGGCGAGGCAGCACACGCCTGCAATCCCAGCACTTTGG CCTCATTAGTAAGATCTTTCATTAGCTGGGCGTGGCAGCACACGCCTGCAATCCCAGCACTTTGG T A AKAP8 Ensembl:ENSG00000105127 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1255313118 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17567973 RMVar_hsa_circ_33045,RMVar_hsa_circ_267662,RMVar_hsa_circ_51564 2084 RMVar_ID_2084 Human_SNP_ID_659598169 A-to-I Human chr19 - 15376278 15376278 15376278 ACTCCTGACCTCATAATCAATCCCATAATCAAAGTGCTGGGATTACAGGCGTGAGCCACCACGCC ACTCCTGACCTCATAATCAATCCCATAATCAAGGTGCTGGGATTACAGGCGTGAGCCACCACGCC T C AKAP8 Ensembl:ENSG00000105127 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1262607085 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17916162 RMVar_hsa_circ_33045,RMVar_hsa_circ_267662,RMVar_hsa_circ_51564 2085 RMVar_ID_2085 Human_SNP_ID_659600408 A-to-I Human chr19 - 15382774 15382774 15382774 GTGGCTGGTCGCAAGTGAAATCATTGCACACTATAGCCTTGAACTCCTGAACTTGAGCAATCCTC GTGGCTGGTCGCAAGTGAAATCATTGCACACTGTAGCCTTGAACTCCTGAACTTGAGCAATCCTC T C AKAP8L Ensembl:ENSG00000011243 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1568260001 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13382437 RMVar_hsa_circ_26700,RMVar_hsa_circ_118166,RMVar_hsa_circ_265663,RMVar_hsa_circ_51331,RMVar_hsa_circ_193137 2086 RMVar_ID_2086 Human_SNP_ID_659601553 A-to-I Human chr19 - 15386724 15386724 15386724 AACCCGGGAAGTAGAGGTTGCAGTGAGCCGATATCACGCCATTGCACTCCAGCCTGGGCAACCAA AACCCGGGAAGTAGAGGTTGCAGTGAGCCGATCTCACGCCATTGCACTCCAGCCTGGGCAACCAA T G AKAP8L Ensembl:ENSG00000011243 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1481674081 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25387003 RMVar_hsa_circ_26700,RMVar_hsa_circ_118166,RMVar_hsa_circ_265663,RMVar_hsa_circ_51331,RMVar_hsa_circ_193137 2087 RMVar_ID_2087 Human_SNP_ID_659601592 A-to-I Human chr19 - 15386838 15386838 15386838 CCTGGACAACATCGTGAAACCCCATCTTTACTAAAAATACAAAAATTAGCCGGGCTTGGTGGCGG CCTGGACAACATCGTGAAACCCCATCTTTACTGAAAATACAAAAATTAGCCGGGCTTGGTGGCGG T C AKAP8L Ensembl:ENSG00000011243 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs895363921 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26700,RMVar_hsa_circ_118166,RMVar_hsa_circ_265663,RMVar_hsa_circ_51331,RMVar_hsa_circ_193137 2088 RMVar_ID_2088 Human_SNP_ID_659601826 A-to-I Human chr19 - 15387810 15387810 15387810 GGATTACAGGCATGTGCTACCACGCCCGGCTAATTTTTGTATTGTTAGTAGAGACGGGGTTTCAC GGATTACAGGCATGTGCTACCACGCCCGGCTAGTTTTTGTATTGTTAGTAGAGACGGGGTTTCAC T C AKAP8L Ensembl:ENSG00000011243 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025815229 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26700,RMVar_hsa_circ_118166,RMVar_hsa_circ_265663,RMVar_hsa_circ_51331,RMVar_hsa_circ_193137 2089 RMVar_ID_2089 Human_SNP_ID_659601827 A-to-I Human chr19 - 15387810 15387810 15387810 GGATTACAGGCATGTGCTACCACGCCCGGCTAATTTTTGTATTGTTAGTAGAGACGGGGTTTCAC GGATTACAGGCATGTGCTACCACGCCCGGCTACTTTTTGTATTGTTAGTAGAGACGGGGTTTCAC T G AKAP8L Ensembl:ENSG00000011243 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025815229 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26700,RMVar_hsa_circ_118166,RMVar_hsa_circ_265663,RMVar_hsa_circ_51331,RMVar_hsa_circ_193137 2090 RMVar_ID_2090 Human_SNP_ID_659601839 A-to-I Human chr19 - 15387835 15387835 15387835 CCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCATGTGCTACCACGCCCGGCTAATTTTTGT CCTGCCTCAGCCTCCCGAGTAGCTGGGATTACGGGCATGTGCTACCACGCCCGGCTAATTTTTGT T C AKAP8L Ensembl:ENSG00000011243 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1357166014 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26700,RMVar_hsa_circ_118166,RMVar_hsa_circ_265663,RMVar_hsa_circ_51331,RMVar_hsa_circ_193137 2091 RMVar_ID_2091 Human_SNP_ID_659602602 A-to-I Human chr19 - 15390337 15390337 15390337 TCGGCTCACTGCAACCTCCACCTCTCAGGCTCAGGCGATCCTCACACCTCAGCCTCCCAAATAGC TCGGCTCACTGCAACCTCCACCTCTCAGGCTCCGGCGATCCTCACACCTCAGCCTCCCAAATAGC T G AKAP8L Ensembl:ENSG00000011243 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1328321687 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26700,RMVar_hsa_circ_118166,RMVar_hsa_circ_265663,RMVar_hsa_circ_51331,RMVar_hsa_circ_193137 2092 RMVar_ID_2092 Human_SNP_ID_659608133 A-to-I Human chr19 - 15410875 15410875 15410875 CTGGAAGGTCGAGGTTGCAGTGAGCCGTGATCATGCCACTGCGTTGCAGCCCGGACAGAGTGAGA CTGGAAGGTCGAGGTTGCAGTGAGCCGTGATCGTGCCACTGCGTTGCAGCCCGGACAGAGTGAGA T C AKAP8L Ensembl:ENSG00000011243 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1212003894 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13382966 2093 RMVar_ID_2093 Human_SNP_ID_659609228 A-to-I Human chr19 - 15415371 15415371 15415371 GAGTGCAGTGGCACAAAATCATAGCTCACTGCAGCCTCGCCCTCCTGTGCTCAAGTAATCCTCCC GAGTGCAGTGGCACAAAATCATAGCTCACTGCGGCCTCGCCCTCCTGTGCTCAAGTAATCCTCCC T C AKAP8L Ensembl:ENSG00000011243 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs774129000 Functional Loss SNV dbSNP153 33..33 33 - - - 2094 RMVar_ID_2094 Human_SNP_ID_659609253 A-to-I Human chr19 - 15415521 15415521 15415521 ATGCCATTGCACTCCAGCCTGGGCAACAGAGCAAGATCCTGTCTCAAGAAAATATATACTCTTTT ATGCCATTGCACTCCAGCCTGGGCAACAGAGCGAGATCCTGTCTCAAGAAAATATATACTCTTTT T C AKAP8L Ensembl:ENSG00000011243 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1048594062 Functional Loss SNV dbSNP153 33..33 33 - - - 2095 RMVar_ID_2095 Human_SNP_ID_659609254 A-to-I Human chr19 - 15415521 15415521 15415521 ATGCCATTGCACTCCAGCCTGGGCAACAGAGCAAGATCCTGTCTCAAGAAAATATATACTCTTTT ATGCCATTGCACTCCAGCCTGGGCAACAGAGCCAGATCCTGTCTCAAGAAAATATATACTCTTTT T G AKAP8L Ensembl:ENSG00000011243 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1048594062 Functional Loss SNV dbSNP153 33..33 33 - - - 2096 RMVar_ID_2096 Human_SNP_ID_659609291 A-to-I Human chr19 - 15415643 15415643 15415643 TGACCTTGTGATCCGCCCTCCCTGGCCTCCCAAGGTGCTGGGATTACGGGCATGAGCCACTGCGC TGACCTTGTGATCCGCCCTCCCTGGCCTCCCAGGGTGCTGGGATTACGGGCATGAGCCACTGCGC T C AKAP8L Ensembl:ENSG00000011243 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs902179566 Functional Loss SNV dbSNP153 33..33 33 - - - 2097 RMVar_ID_2097 Human_SNP_ID_659667309 A-to-I Human chr19 + 15621419 15621419 15621419 GTGGTGGTGCGTGCCTGTAACCCCAGCTACTCAGGAGGCTGAGACAGGAGAATTGCTTGAACCCA GTGGTGGTGCGTGCCTGTAACCCCAGCTACTCGGGAGGCTGAGACAGGAGAATTGCTTGAACCCA A G CYP4F8 Ensembl:ENSG00000186526 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1388826688 Functional Loss SNV dbSNP153 33..33 33 - - - 2098 RMVar_ID_2098 Human_SNP_ID_659679425 A-to-I Human chr19 + 15660856 15660856 15660856 GTCCTGTCTCAGCCTCCCAAGTAGCTGGGATTACAGGCACCCACCACCACATCCAGCTAATTGTT GTCCTGTCTCAGCCTCCCAAGTAGCTGGGATTGCAGGCACCCACCACCACATCCAGCTAATTGTT A G CYP4F3 Ensembl:ENSG00000186529 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1225060780 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93205,RMVar_hsa_circ_193145 2099 RMVar_ID_2099 Human_SNP_ID_659679499 A-to-I Human chr19 + 15661098 15661098 15661098 TAACAGCAATGAGAACTTAGGCTCCCCTCTCTACTAAAATACAAAAGTTAGCTGGTCATGGTGGT TAACAGCAATGAGAACTTAGGCTCCCCTCTCTTCTAAAATACAAAAGTTAGCTGGTCATGGTGGT A T CYP4F3 Ensembl:ENSG00000186529 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1399862291 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93205,RMVar_hsa_circ_193145 2100 RMVar_ID_2100 Human_SNP_ID_659679510 A-to-I Human chr19 + 15661141 15661141 15661141 AAAGTTAGCTGGTCATGGTGGTGCGGGCCTGTAATCCCAGCTACTCGGGAGGCTGATGCGGGAGA AAAGTTAGCTGGTCATGGTGGTGCGGGCCTGTGATCCCAGCTACTCGGGAGGCTGATGCGGGAGA A G CYP4F3 Ensembl:ENSG00000186529 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1207740782 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93205,RMVar_hsa_circ_193145 2101 RMVar_ID_2101 Human_SNP_ID_659679525 A-to-I Human chr19 + 15661207 15661207 15661207 TCACTTGAAACCCACAGGCGGAGGTTGCAGTGAGCTGAGGTGGTGCCACTACGCTCCAGCCTGGG TCACTTGAAACCCACAGGCGGAGGTTGCAGTGGGCTGAGGTGGTGCCACTACGCTCCAGCCTGGG A G CYP4F3 Ensembl:ENSG00000186529 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1140860 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1971650 RMVar_hsa_circ_93205,RMVar_hsa_circ_193145 2102 RMVar_ID_2102 Human_SNP_ID_659679526 A-to-I Human chr19 + 15661212 15661212 15661212 TGAAACCCACAGGCGGAGGTTGCAGTGAGCTGAGGTGGTGCCACTACGCTCCAGCCTGGGGGAGG TGAAACCCACAGGCGGAGGTTGCAGTGAGCTGGGGTGGTGCCACTACGCTCCAGCCTGGGGGAGG A G CYP4F3 Ensembl:ENSG00000186529 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1140861 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1971650 RMVar_hsa_circ_93205,RMVar_hsa_circ_193145 2103 RMVar_ID_2103 Human_SNP_ID_659798371 A-to-I Human chr19 + 16078047 16078047 16078047 TGCCCACCTTGGCCTCCCAAAGTTCTGGGATTACAAGCGTGAGCCACGGCGCCCAGCCTCAATTG TGCCCACCTTGGCCTCCCAAAGTTCTGGGATTCCAAGCGTGAGCCACGGCGCCCAGCCTCAATTG A C TPM4 Ensembl:ENSG00000167460 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1237104328 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1093709,Human_RBP_ID_13384202 Human_Splice_Rec_1972896,Human_Splice_Rec_1972960 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 2104 RMVar_ID_2104 Human_SNP_ID_659798886 A-to-I Human chr19 + 16079774 16079774 16079774 CAGGCTGGAGTGCAGTGGCGCGATCTCGGCTCATTGCAACCTTCACCTCCCGGGTTCAAGCGATT CAGGCTGGAGTGCAGTGGCGCGATCTCGGCTCCTTGCAACCTTCACCTCCCGGGTTCAAGCGATT A C TPM4 Ensembl:ENSG00000167460 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1048538016 Functional Loss SNV dbSNP153 33..33 33 - - - 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 2105 RMVar_ID_2105 Human_SNP_ID_659798887 A-to-I Human chr19 + 16079774 16079774 16079774 CAGGCTGGAGTGCAGTGGCGCGATCTCGGCTCATTGCAACCTTCACCTCCCGGGTTCAAGCGATT CAGGCTGGAGTGCAGTGGCGCGATCTCGGCTCGTTGCAACCTTCACCTCCCGGGTTCAAGCGATT A G TPM4 Ensembl:ENSG00000167460 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1048538016 Functional Loss SNV dbSNP153 33..33 33 - - - 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 2106 RMVar_ID_2106 Human_SNP_ID_659799121 A-to-I Human chr19 + 16080601 16080601 16080601 GGGAGACCAAGGCGGGTGGATCACGTGAGGCCAGGAGTTTGAGACCAGCCTGACCAACAAGACGA GGGAGACCAAGGCGGGTGGATCACGTGAGGCCGGGAGTTTGAGACCAGCCTGACCAACAAGACGA A G TPM4 Ensembl:ENSG00000167460 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs994286874 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25387380 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 2107 RMVar_ID_2107 Human_SNP_ID_659799343 A-to-I Human chr19 + 16081465 16081465 16081465 GTCACCAGGCTGGAGTGCAGTGGCACGATCTCAGCTCACGGCAACCTCCGCCTCCCGGGTTCAAG GTCACCAGGCTGGAGTGCAGTGGCACGATCTCGGCTCACGGCAACCTCCGCCTCCCGGGTTCAAG A G TPM4 Ensembl:ENSG00000167460 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs991497794 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1973030 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_193156 2108 RMVar_ID_2108 Human_SNP_ID_659799372 A-to-I Human chr19 + 16081561 16081561 16081561 GGAACTACAGGCACGTGCCACCACACTCAGCTAATTTTTCTATTTTTAGTAGAGACAGGGTTTCA GGAACTACAGGCACGTGCCACCACACTCAGCTGATTTTTCTATTTTTAGTAGAGACAGGGTTTCA A G TPM4 Ensembl:ENSG00000167460 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1218026070 Functional Loss SNV dbSNP153 33..33 33 - - - 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_193156 2109 RMVar_ID_2109 Human_SNP_ID_659799877 A-to-I Human chr19 + 16083257 16083257 16083257 ACTGAGGTCAGGTGTTTGAGACCAGACTGGCCAACATGGTGAAACCCCGTCTCTATTAAAAATAC ACTGAGGTCAGGTGTTTGAGACCAGACTGGCCGACATGGTGAAACCCCGTCTCTATTAAAAATAC A G TPM4 Ensembl:ENSG00000167460 Protein coding intron GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-Seq:(High) rs1045215576 Functional Loss SNV dbSNP153 33..33 33 - - - 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_282739,RMVar_hsa_circ_118552,RMVar_hsa_circ_267670,RMVar_hsa_circ_193160,RMVar_hsa_circ_193161,RMVar_hsa_circ_193158 2110 RMVar_ID_2110 Human_SNP_ID_659799904 A-to-I Human chr19 + 16083391 16083391 16083391 CAGCTTGAACCCAGGAGGCAGAGGGTGCAGTGAGCCAAGATCGCACCACTGCACTCCAGCCTGGG CAGCTTGAACCCAGGAGGCAGAGGGTGCAGTGGGCCAAGATCGCACCACTGCACTCCAGCCTGGG A G TPM4 Ensembl:ENSG00000167460 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1049541181 Functional Loss SNV dbSNP153 33..33 33 - - - 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_282739,RMVar_hsa_circ_118552,RMVar_hsa_circ_267670,RMVar_hsa_circ_193160,RMVar_hsa_circ_193161,RMVar_hsa_circ_193158 2111 RMVar_ID_2111 Human_SNP_ID_659800125 A-to-I Human chr19 + 16084109 16084100 16084109 CCACCACACCCGGCTAATTTTTTTGTATTTTTAGTAGAGACAGGGTTTCACCGTGTTAGCCACGA CCACCACACCCGGCTAATTTTTTT_________GTAGAGACAGGGTTTCACCGTGTTAGCCACGA TGTATTTTTA T TPM4 Ensembl:ENSG00000167460 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1294668113 Functional Loss DEL dbSNP153 25..33 33 - - - 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_282739,RMVar_hsa_circ_118552,RMVar_hsa_circ_267670,RMVar_hsa_circ_193160,RMVar_hsa_circ_193161,RMVar_hsa_circ_193158 2112 RMVar_ID_2112 Human_SNP_ID_659800595 A-to-I Human chr19 + 16085989 16085989 16085989 TATGCTGGAGGCTGAGACAGGAGAATTGCTTGAACCCAGGAGATGGAGGCTGCAGTGAGCTGAGA TATGCTGGAGGCTGAGACAGGAGAATTGCTTGTACCCAGGAGATGGAGGCTGCAGTGAGCTGAGA A T TPM4 Ensembl:ENSG00000167460 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs911259497 Functional Loss SNV dbSNP153 33..33 33 - - - 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_282739,RMVar_hsa_circ_118552,RMVar_hsa_circ_267670,RMVar_hsa_circ_193160,RMVar_hsa_circ_193161,RMVar_hsa_circ_193158 2113 RMVar_ID_2113 Human_SNP_ID_659802151 A-to-I Human chr19 + 16091565 16091565 16091565 AGGAAGCCGAGGCGGGAGGATCGCTTGAGCTCAGAAGTTCGAGACCAGCCTGGGCAACATGGAGA AGGAAGCCGAGGCGGGAGGATCGCTTGAGCTCCGAAGTTCGAGACCAGCCTGGGCAACATGGAGA A C TPM4 Ensembl:ENSG00000167460 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1440494075 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_30749,RMVar_hsa_circ_77943,RMVar_hsa_circ_193152,RMVar_hsa_circ_123078,RMVar_hsa_circ_311721,RMVar_hsa_circ_193156,RMVar_hsa_circ_267670,RMVar_hsa_circ_193161,RMVar_hsa_circ_193163,RMVar_hsa_circ_122071,RMVar_hsa_circ_324265,RMVar_hsa_circ_193164,RMVar_hsa_circ_368537 2114 RMVar_ID_2114 Human_SNP_ID_659802259 A-to-I Human chr19 + 16092077 16092076 16092078 CCTGTAGGCCCAGCTACTTGGGAGGCTGAGTCAGGGGAATTGCTTCAGCCTGGGAGGCAGAAGTT CCTGTAGGCCCAGCTACTTGGGAGGCTGAGTC__GGGAATTGCTTCAGCCTGGGAGGCAGAAGTT CAG C TPM4 Ensembl:ENSG00000167460 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1011728197 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_30749,RMVar_hsa_circ_77943,RMVar_hsa_circ_193152,RMVar_hsa_circ_123078,RMVar_hsa_circ_311721,RMVar_hsa_circ_193156,RMVar_hsa_circ_267670,RMVar_hsa_circ_193161,RMVar_hsa_circ_193163,RMVar_hsa_circ_122071,RMVar_hsa_circ_324265,RMVar_hsa_circ_193164,RMVar_hsa_circ_368537 2115 RMVar_ID_2115 Human_SNP_ID_659803691 A-to-I Human chr19 + 16097134 16097134 16097134 GACCACCACACTCAGCTAATTTTTGTACTTTCAGTAGAGATGGGGTTTCACCATGTTAGCTAGGC GACCACCACACTCAGCTAATTTTTGTACTTTCGGTAGAGATGGGGTTTCACCATGTTAGCTAGGC A G TPM4 Ensembl:ENSG00000167460 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1362834163 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77943,RMVar_hsa_circ_193152,RMVar_hsa_circ_123078,RMVar_hsa_circ_193156,RMVar_hsa_circ_267670,RMVar_hsa_circ_193163,RMVar_hsa_circ_122071,RMVar_hsa_circ_368537,RMVar_hsa_circ_113398,RMVar_hsa_circ_335366,RMVar_hsa_circ_193167 2116 RMVar_ID_2116 Human_SNP_ID_659803956 A-to-I Human chr19 + 16098278 16098278 16098278 CAACCTGGTCAACATGGTGAAACTCTGTCTCTACTAAAAATGCAAAAATTAGCCGGGCATGGTCA CAACCTGGTCAACATGGTGAAACTCTGTCTCTTCTAAAAATGCAAAAATTAGCCGGGCATGGTCA A T TPM4 Ensembl:ENSG00000167460 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1298613604 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77943,RMVar_hsa_circ_193152,RMVar_hsa_circ_123078,RMVar_hsa_circ_193156,RMVar_hsa_circ_267670,RMVar_hsa_circ_193163,RMVar_hsa_circ_122071,RMVar_hsa_circ_368537,RMVar_hsa_circ_113398,RMVar_hsa_circ_335366,RMVar_hsa_circ_193167 2117 RMVar_ID_2117 Human_SNP_ID_659804272 A-to-I Human chr19 + 16099419 16099419 16099419 CAGCTTGGGCAACATGGCGAAACCCCATCTCTACTAAAAATACAAGAATTGGCTGGGTGTAGTGG CAGCTTGGGCAACATGGCGAAACCCCATCTCTGCTAAAAATACAAGAATTGGCTGGGTGTAGTGG A G TPM4 Ensembl:ENSG00000167460 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs891752190 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23784802 RMVar_hsa_circ_77943,RMVar_hsa_circ_193152,RMVar_hsa_circ_123078,RMVar_hsa_circ_193156,RMVar_hsa_circ_267670,RMVar_hsa_circ_193163,RMVar_hsa_circ_122071,RMVar_hsa_circ_368537,RMVar_hsa_circ_113398,RMVar_hsa_circ_335366,RMVar_hsa_circ_193167 2118 RMVar_ID_2118 Human_SNP_ID_659804283 A-to-I Human chr19 + 16099473 16099473 16099473 GGGTGTAGTGGCACGCACTTGTAGTCCCAGCTACTTGGGAGGCTGAGGTAGAAGGATCACTTGAG GGGTGTAGTGGCACGCACTTGTAGTCCCAGCTGCTTGGGAGGCTGAGGTAGAAGGATCACTTGAG A G TPM4 Ensembl:ENSG00000167460 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs867834069 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77943,RMVar_hsa_circ_193152,RMVar_hsa_circ_123078,RMVar_hsa_circ_193156,RMVar_hsa_circ_267670,RMVar_hsa_circ_193163,RMVar_hsa_circ_122071,RMVar_hsa_circ_368537,RMVar_hsa_circ_113398,RMVar_hsa_circ_335366,RMVar_hsa_circ_193167 2119 RMVar_ID_2119 Human_SNP_ID_659804463 A-to-I Human chr19 + 16100285 16100285 16100285 CTCAAGGGTTACCAGAGTTCACAAGGAAAAATACAGGACACCAACTTAAATCTGAGTTTCAGATA CTCAAGGGTTACCAGAGTTCACAAGGAAAAATGCAGGACACCAACTTAAATCTGAGTTTCAGATA A G TPM4 Ensembl:ENSG00000167460 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs998446262 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77943,RMVar_hsa_circ_193152,RMVar_hsa_circ_123078,RMVar_hsa_circ_193156,RMVar_hsa_circ_267670,RMVar_hsa_circ_193163,RMVar_hsa_circ_122071,RMVar_hsa_circ_368537,RMVar_hsa_circ_113398,RMVar_hsa_circ_335366,RMVar_hsa_circ_193167 2120 RMVar_ID_2120 Human_SNP_ID_659808861 A-to-I Human chr19 + 16117358 16117358 16117358 TAAAAACTCAAAAATTGGCCGGGCATTGTGGCAGGCACCTGTGGTCCCAGCTACTCGGGAGGCTG TAAAAACTCAAAAATTGGCCGGGCATTGTGGCGGGCACCTGTGGTCCCAGCTACTCGGGAGGCTG A G RAB8A Ensembl:ENSG00000167461 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs775960071 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122746,RMVar_hsa_circ_193168,RMVar_hsa_circ_103403,RMVar_hsa_circ_193169 2121 RMVar_ID_2121 Human_SNP_ID_659816713 A-to-I Human chr19 + 16146943 16146943 16146943 TGCCTCCTGAGTTCTAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCACCCA TGCCTCCTGAGTTCTAGCAATTCTCCTGCCTCTGCCTCCTGAGTAGCTGGGATTACAGGCACCCA A T HSH2D Ensembl:ENSG00000196684 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1407115137 Functional Loss SNV dbSNP153 33..33 33 - - - 2122 RMVar_ID_2122 Human_SNP_ID_659816715 A-to-I Human chr19 + 16146955 16146955 16146955 TCTAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCACCCACCACCTCATCTG TCTAGCAATTCTCCTGCCTCAGCCTCCTGAGTTGCTGGGATTACAGGCACCCACCACCTCATCTG A T HSH2D Ensembl:ENSG00000196684 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs927518750 Functional Loss SNV dbSNP153 33..33 33 - - - 2123 RMVar_ID_2123 Human_SNP_ID_659816791 A-to-I Human chr19 + 16147286 16147286 16147286 ACAGGTGGATTTCTTGAGTCCAGGAGTTTGAGACCAATGTGGGCAGCAAGGTGAAACCCCATCTC ACAGGTGGATTTCTTGAGTCCAGGAGTTTGAGTCCAATGTGGGCAGCAAGGTGAAACCCCATCTC A T HSH2D Ensembl:ENSG00000196684 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1488171628 Functional Loss SNV dbSNP153 33..33 33 - - - 2124 RMVar_ID_2124 Human_SNP_ID_659817617 A-to-I Human chr19 + 16150641 16150640 16150641 GGAGACTTGCTGGAACCCTGCAGGCAGAGATCATGCCACTGCACTCCAGCCTGGGTGACAGAGCA GGAGACTTGCTGGAACCCTGCAGGCAGAGATTGTGCCACTGCACTCCAGCCTGGGTGACAGAGCA CA TG HSH2D Ensembl:ENSG00000196684 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs386807308 Functional Loss MNV dbSNP153 32..33 33 - - - RMVar_hsa_circ_99067,RMVar_hsa_circ_193174 2125 RMVar_ID_2125 Human_SNP_ID_659817619 A-to-I Human chr19 + 16150641 16150641 16150641 GGAGACTTGCTGGAACCCTGCAGGCAGAGATCATGCCACTGCACTCCAGCCTGGGTGACAGAGCA GGAGACTTGCTGGAACCCTGCAGGCAGAGATCGTGCCACTGCACTCCAGCCTGGGTGACAGAGCA A G HSH2D Ensembl:ENSG00000196684 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs166948 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99067,RMVar_hsa_circ_193174 2126 RMVar_ID_2126 Human_SNP_ID_659819307 A-to-I Human chr19 + 16156082 16156082 16156082 TGTGGAAAGAAACATGGATATTTGGTCTGCGTAGTGGCTCACACCTGTATTCCCAGTGCTTTGGG TGTGGAAAGAAACATGGATATTTGGTCTGCGTGGTGGCTCACACCTGTATTCCCAGTGCTTTGGG A G HSH2D Ensembl:ENSG00000196684 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1325080035 Functional Loss SNV dbSNP153 33..33 33 - - - 2127 RMVar_ID_2127 Human_SNP_ID_659819308 A-to-I Human chr19 + 16156082 16156082 16156082 TGTGGAAAGAAACATGGATATTTGGTCTGCGTAGTGGCTCACACCTGTATTCCCAGTGCTTTGGG TGTGGAAAGAAACATGGATATTTGGTCTGCGTTGTGGCTCACACCTGTATTCCCAGTGCTTTGGG A T HSH2D Ensembl:ENSG00000196684 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1325080035 Functional Loss SNV dbSNP153 33..33 33 - - - 2128 RMVar_ID_2128 Human_SNP_ID_659819349 A-to-I Human chr19 + 16156235 16156235 16156235 TTAGCCAGGCATGGTGGCGCACGCCTGTAGTCAGCTACTCTGGGGGCTGAGGTGGGAGGATTGCT TTAGCCAGGCATGGTGGCGCACGCCTGTAGTCGGCTACTCTGGGGGCTGAGGTGGGAGGATTGCT A G HSH2D Ensembl:ENSG00000196684 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1327795430 Functional Loss SNV dbSNP153 33..33 33 - - - 2129 RMVar_ID_2129 Human_SNP_ID_659828221 A-to-I Human chr19 + 16188569 16188569 16188569 GCCCAGGAGTTCAGGACTAGCCTGGGCAACATAGCGATACCCTGTCTCTTCAAAAACTAAAATAG GCCCAGGAGTTCAGGACTAGCCTGGGCAACATGGCGATACCCTGTCTCTTCAAAAACTAAAATAG A G FAM32A Ensembl:ENSG00000105058 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs778451703 Functional Loss SNV dbSNP153 33..33 33 - - - 2130 RMVar_ID_2130 Human_SNP_ID_659835423 A-to-I Human chr19 + 16216402 16216402 16216402 AGGAGGCGGAGCTTGCAGTGAGCCGAGATTGCACCACTGCCCTCCAGCCTGGGCGACAGAGCGAA AGGAGGCGGAGCTTGCAGTGAGCCGAGATTGCCCCACTGCCCTCCAGCCTGGGCGACAGAGCGAA A C AP1M1 Ensembl:ENSG00000072958 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs962325467 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25442490 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_193181 2131 RMVar_ID_2131 Human_SNP_ID_659884873 A-to-I Human chr19 - 16397142 16397142 16397142 GAGGTTGCAGTGAGCCGAGATCACGCCACTGCACTCCAGCCTGGATGACAAGAGTGAAACTCTGT GAGGTTGCAGTGAGCCGAGATCACGCCACTGCCCTCCAGCCTGGATGACAAGAGTGAAACTCTGT T G EPS15L1 Ensembl:ENSG00000127527 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs561506145 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_137939 RMVar_hsa_circ_54665,RMVar_hsa_circ_266066,RMVar_hsa_circ_32946,RMVar_hsa_circ_51548,RMVar_hsa_circ_8959,RMVar_hsa_circ_19894,RMVar_hsa_circ_269778,RMVar_hsa_circ_24155,RMVar_hsa_circ_369489,RMVar_hsa_circ_193191 2132 RMVar_ID_2132 Human_SNP_ID_659884892 A-to-I Human chr19 - 16397214 16397214 16397214 ATGGTGGTGCACGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCCG ATGGTGGTGCACGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCCG T C EPS15L1 Ensembl:ENSG00000127527 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1313149118 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_137939 RMVar_hsa_circ_54665,RMVar_hsa_circ_266066,RMVar_hsa_circ_32946,RMVar_hsa_circ_51548,RMVar_hsa_circ_8959,RMVar_hsa_circ_19894,RMVar_hsa_circ_269778,RMVar_hsa_circ_24155,RMVar_hsa_circ_369489,RMVar_hsa_circ_193191 2133 RMVar_ID_2133 Human_SNP_ID_659884893 A-to-I Human chr19 - 16397218 16397218 16397218 GGGCATGGTGGTGCACGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAA GGGCATGGTGGTGCACGCCTGTAATCCCAGCTGCTCAGGAGGCTGAGGCAGGAGAATCACTTGAA T C EPS15L1 Ensembl:ENSG00000127527 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs531169655 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_137939 RMVar_hsa_circ_54665,RMVar_hsa_circ_266066,RMVar_hsa_circ_32946,RMVar_hsa_circ_51548,RMVar_hsa_circ_8959,RMVar_hsa_circ_19894,RMVar_hsa_circ_269778,RMVar_hsa_circ_24155,RMVar_hsa_circ_369489,RMVar_hsa_circ_193191 2134 RMVar_ID_2134 Human_SNP_ID_659884894 A-to-I Human chr19 - 16397218 16397218 16397218 GGGCATGGTGGTGCACGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAA GGGCATGGTGGTGCACGCCTGTAATCCCAGCTCCTCAGGAGGCTGAGGCAGGAGAATCACTTGAA T G EPS15L1 Ensembl:ENSG00000127527 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs531169655 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_137939 RMVar_hsa_circ_54665,RMVar_hsa_circ_266066,RMVar_hsa_circ_32946,RMVar_hsa_circ_51548,RMVar_hsa_circ_8959,RMVar_hsa_circ_19894,RMVar_hsa_circ_269778,RMVar_hsa_circ_24155,RMVar_hsa_circ_369489,RMVar_hsa_circ_193191 2135 RMVar_ID_2135 Human_SNP_ID_659885578 A-to-I Human chr19 - 16400080 16400080 16400080 TGCCCGCCTCGACCTCCCCAAATGCTGGGATTACAGGCGTGAGCCACCTCACCCGCCAAAGTCAG TGCCCGCCTCGACCTCCCCAAATGCTGGGATTGCAGGCGTGAGCCACCTCACCCGCCAAAGTCAG T C EPS15L1 Ensembl:ENSG00000127527 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs544826228 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25387777 RMVar_hsa_circ_54665,RMVar_hsa_circ_266066,RMVar_hsa_circ_32946,RMVar_hsa_circ_51548,RMVar_hsa_circ_8959,RMVar_hsa_circ_19894,RMVar_hsa_circ_269778,RMVar_hsa_circ_24155,RMVar_hsa_circ_369489,RMVar_hsa_circ_193191 2136 RMVar_ID_2136 Human_SNP_ID_659885600 A-to-I Human chr19 - 16400171 16400171 16400171 CACCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGACGAGGTTTCACAGTGTTGCCCAGGCTGG CACCATGCCCAGCTAATTTTTGTATTTTTAGTTGAGACGAGGTTTCACAGTGTTGCCCAGGCTGG T A EPS15L1 Ensembl:ENSG00000127527 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202715579 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13386044 RMVar_hsa_circ_54665,RMVar_hsa_circ_266066,RMVar_hsa_circ_32946,RMVar_hsa_circ_51548,RMVar_hsa_circ_8959,RMVar_hsa_circ_19894,RMVar_hsa_circ_269778,RMVar_hsa_circ_24155,RMVar_hsa_circ_369489,RMVar_hsa_circ_193191 2137 RMVar_ID_2137 Human_SNP_ID_659891989 A-to-I Human chr19 - 16424554 16424554 16424554 CTCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGTGCCCAGCCTGTGTCT CTCCTGCCTCGGCCTCCCAAAGTGCTGGGATTGCAGGTGTGAGCCACCGTGCCCAGCCTGTGTCT T C EPS15L1 Ensembl:ENSG00000127527 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs986208637 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9063,RMVar_hsa_circ_19894,RMVar_hsa_circ_269778,RMVar_hsa_circ_266646,RMVar_hsa_circ_56521,RMVar_hsa_circ_10513,RMVar_hsa_circ_49795 2138 RMVar_ID_2138 Human_SNP_ID_659903766 A-to-I Human chr19 - 16468801 16468801 16468801 TGCTATGCTGCCTAGGCAGGTCTTAAACCCCTAGCCTCAAGCAATCCTTCTATCTCAGCCTCCTA TGCTATGCTGCCTAGGCAGGTCTTAAACCCCTTGCCTCAAGCAATCCTTCTATCTCAGCCTCCTA T A EPS15L1 Ensembl:ENSG00000127527 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251162632 Functional Loss SNV dbSNP153 33..33 33 - - - 2139 RMVar_ID_2139 Human_SNP_ID_659920837 A-to-I Human chr19 - 16528837 16528837 16528837 GCCATTCTCCTACCTCAGCCTCCTGAGTAGCTAGGACTACAGGCGCACGCAACCATGCCCAGCTA GCCATTCTCCTACCTCAGCCTCCTGAGTAGCTGGGACTACAGGCGCACGCAACCATGCCCAGCTA T C CHERP,AC008764.1 Ensembl:ENSG00000085872,Ensembl:ENSG00000141979 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1158125371 Functional Loss SNV dbSNP153 33..33 33 - - - 2140 RMVar_ID_2140 Human_SNP_ID_659921405 A-to-I Human chr19 - 16530618 16530618 16530618 GGCTACTTCGATGACTCCATCATTCAGCAGCTACAGAGCCCAGCCCTGGGGCTTGGTCAGTACCA GGCTACTTCGATGACTCCATCATTCAGCAGCTGCAGAGCCCAGCCCTGGGGCTTGGTCAGTACCA T C CHERP,AC008764.1 Ensembl:ENSG00000085872,Ensembl:ENSG00000141979 Protein coding,Protein coding CDS,intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1295313818 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54932,Human_RBP_ID_279281,Human_RBP_ID_1013565,Human_RBP_ID_3956478,Human_RBP_ID_8839181,Human_RBP_ID_17272631,Human_RBP_ID_18994551,Human_RBP_ID_27815264 Human_Splice_Rec_1973964,Human_Splice_Rec_1973965,Human_Splice_Rec_1973996,Human_Splice_Rec_1973997 RMVar_hsa_circ_267066 2141 RMVar_ID_2141 Human_SNP_ID_659922696 A-to-I Human chr19 - 16534604 16534604 16534604 GGGCGTGGTGGTGCACGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATTGCTTCAA GGGCGTGGTGGTGCACGCCTGTAATCCCAGCTGCTTGGGAGGCTGAGGCAGGAGAATTGCTTCAA T C CHERP,AC008764.1 Ensembl:ENSG00000085872,Ensembl:ENSG00000141979 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1307478839 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267066,RMVar_hsa_circ_378968 2142 RMVar_ID_2142 Human_SNP_ID_659925639 A-to-I Human chr19 - 16543772 16543772 16543772 TGCTTGAGCACGGGAGGCAGAGGTTGCAGTGAACCGAGATCACACCACTGCACTCCAGCTTGGGC TGCTTGAGCACGGGAGGCAGAGGTTGCAGTGAGCCGAGATCACACCACTGCACTCCAGCTTGGGC T C AC008764.1 Ensembl:ENSG00000141979 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1274422988 Functional Loss SNV dbSNP153 33..33 33 - - - 2143 RMVar_ID_2143 Human_SNP_ID_659925813 A-to-I Human chr19 + 16544360 16544360 16544360 AATAAAATAAAATAAAAAGAGGAAGAAAGGCCAGGCTCAGTGGCTCATGCCTGTAATTCCAGCAC AATAAAATAAAATAAAAAGAGGAAGAAAGGCCCGGCTCAGTGGCTCATGCCTGTAATTCCAGCAC A C AC008764.6 Ensembl:ENSG00000269399 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1402267583 Functional Loss SNV dbSNP153 33..33 33 - - - 2144 RMVar_ID_2144 Human_SNP_ID_659925860 A-to-I Human chr19 - 16544526 16544526 16544526 CCAAGTGATTCTCGTGCCTCAGCCTCCCAAGTAGATGGGATTACAGGCATCCGCCACCATGCCCG CCAAGTGATTCTCGTGCCTCAGCCTCCCAAGTGGATGGGATTACAGGCATCCGCCACCATGCCCG T C AC008764.1 Ensembl:ENSG00000141979 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1267977556 Functional Loss SNV dbSNP153 33..33 33 - - - 2145 RMVar_ID_2145 Human_SNP_ID_659926122 A-to-I Human chr19 - 16545515 16545515 16545515 TCACCTGAGGTTGGGAGTTTGAGGCCAGTCTGACCAACAGGCAGAAACCCCATCTCTACTAAAAA TCACCTGAGGTTGGGAGTTTGAGGCCAGTCTGCCCAACAGGCAGAAACCCCATCTCTACTAAAAA T G AC008764.1 Ensembl:ENSG00000141979 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1412147350 Functional Loss SNV dbSNP153 33..33 33 - - - 2146 RMVar_ID_2146 Human_SNP_ID_659926189 A-to-I Human chr19 - 16545736 16545736 16545736 GTGATGGCAGGCGCCTGTAATCCCATCTACTTAGGAGGCTGAGGCAGGAGAATCACTTGAGTGTG GTGATGGCAGGCGCCTGTAATCCCATCTACTTTGGAGGCTGAGGCAGGAGAATCACTTGAGTGTG T A AC008764.1 Ensembl:ENSG00000141979 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1270625323 Functional Loss SNV dbSNP153 33..33 33 - - - 2147 RMVar_ID_2147 Human_SNP_ID_659926191 A-to-I Human chr19 - 16545740 16545740 16545740 GGGTGTGATGGCAGGCGCCTGTAATCCCATCTACTTAGGAGGCTGAGGCAGGAGAATCACTTGAG GGGTGTGATGGCAGGCGCCTGTAATCCCATCTCCTTAGGAGGCTGAGGCAGGAGAATCACTTGAG T G AC008764.1 Ensembl:ENSG00000141979 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs990335887 Functional Loss SNV dbSNP153 33..33 33 - - - 2148 RMVar_ID_2148 Human_SNP_ID_659926214 A-to-I Human chr19 - 16545831 16545831 16545831 AGGGCAGGCAAATCAGTTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCCCGT AGGGCAGGCAAATCAGTTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCCGT T C AC008764.1 Ensembl:ENSG00000141979 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs189587901 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_27 2149 RMVar_ID_2149 Human_SNP_ID_659926227 A-to-I Human chr19 - 16545871 16545871 16545871 ACGGTGGCTCATGCCTGTAATCCCTGCACTTTAGGAAGCCAGGGCAGGCAAATCAGTTGAGGTCA ACGGTGGCTCATGCCTGTAATCCCTGCACTTTGGGAAGCCAGGGCAGGCAAATCAGTTGAGGTCA T C AC008764.1 Ensembl:ENSG00000141979 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1422267060 Functional Loss SNV dbSNP153 33..33 33 - - - 2150 RMVar_ID_2150 Human_SNP_ID_659926690 A-to-I Human chr19 - 16547387 16547384 16547388 TCGGCTTACTACAACCTCCACCTCCAGACTCAAGTGAGTCTCCTGCCTCAGCCTCCCGAGTAGCT TCGGCTTACTACAACCTCCACCTCCAGACTC____GAGTCTCCTGCCTCAGCCTCCCGAGTAGCT CACTT C AC008764.1 Ensembl:ENSG00000141979 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs201616678 Functional Loss DEL dbSNP153 32..35 33 - - - 2151 RMVar_ID_2151 Human_SNP_ID_659926699 A-to-I Human chr19 - 16547409 16547409 16547409 GCTAGAGTACAGTGGTGCAGTCTCGGCTTACTACAACCTCCACCTCCAGACTCAAGTGAGTCTCC GCTAGAGTACAGTGGTGCAGTCTCGGCTTACTGCAACCTCCACCTCCAGACTCAAGTGAGTCTCC T C AC008764.1 Ensembl:ENSG00000141979 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs138829058 Functional Loss SNV dbSNP153 33..33 33 - - - 2152 RMVar_ID_2152 Human_SNP_ID_659926708 A-to-I Human chr19 - 16547438 16547431 16547439 TTTTGAGACAGAGTCACTCTGTTGCCCAGGCTAGAGTACAGTGGTGCAGTCTCGGCTTACTACAA TTTTGAGACAGAGTCACTCTGTTGCCCAGGC________AGTGGTGCAGTCTCGGCTTACTACAA TGTACTCTA T AC008764.1 Ensembl:ENSG00000141979 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1440472004 Functional Loss DEL dbSNP153 32..39 33 - - - 2153 RMVar_ID_2153 Human_SNP_ID_659926718 A-to-I Human chr19 - 16547459 16547454 16547460 GTATCTACTAAGACACTTTTTTTTTGAGACAGAGTCACTCTGTTGCCCAGGCTAGAGTACAGTGG GTATCTACTAAGACACTTTTTTTTTGAGACA______CTCTGTTGCCCAGGCTAGAGTACAGTGG GTGACTC G AC008764.1 Ensembl:ENSG00000141979 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs911974116 Functional Loss DEL dbSNP153 32..37 33 - - - 2154 RMVar_ID_2154 Human_SNP_ID_659926720 A-to-I Human chr19 - 16547465 16547459 16547466 AGGTTTGTATCTACTAAGACACTTTTTTTTTGAGACAGAGTCACTCTGTTGCCCAGGCTAGAGTA AGGTTTGTATCTACTAAGACACTTTTTTTTT_______AGTCACTCTGTTGCCCAGGCTAGAGTA TCTGTCTC T AC008764.1 Ensembl:ENSG00000141979 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1448838734 Functional Loss DEL dbSNP153 32..38 33 - - - 2155 RMVar_ID_2155 Human_SNP_ID_659926775 A-to-I Human chr19 - 16547712 16547712 16547712 TTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAAATCCTGACTT TTTTGTATTTTTAGTAGAGATGGGGTTTCACCGTGTTGGCCAGGCTGGTCTCGAAATCCTGACTT T C AC008764.1 Ensembl:ENSG00000141979 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1332540215 Functional Loss SNV dbSNP153 33..33 33 - - - 2156 RMVar_ID_2156 Human_SNP_ID_659926829 A-to-I Human chr19 - 16547887 16547885 16547887 GCTTTTTTGTTTCTGTTTTTGTTTTGAGACAGAGTCTCGCTCTGTCACCCAGGCTAGAGGGCAGT GCTTTTTTGTTTCTGTTTTTGTTTTGAGACAG__TCTCGCTCTGTCACCCAGGCTAGAGGGCAGT ACT A AC008764.1 Ensembl:ENSG00000141979 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1337744965 Functional Loss DEL dbSNP153 33..34 33 - - - 2157 RMVar_ID_2157 Human_SNP_ID_659926830 A-to-I Human chr19 - 16547887 16547887 16547887 GCTTTTTTGTTTCTGTTTTTGTTTTGAGACAGAGTCTCGCTCTGTCACCCAGGCTAGAGGGCAGT GCTTTTTTGTTTCTGTTTTTGTTTTGAGACAGTGTCTCGCTCTGTCACCCAGGCTAGAGGGCAGT T A AC008764.1 Ensembl:ENSG00000141979 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1248151559 Functional Loss SNV dbSNP153 33..33 33 - - - 2158 RMVar_ID_2158 Human_SNP_ID_659926977 A-to-I Human chr19 - 16548439 16548439 16548439 GGTCAGGAGTGCAAAACCAGCCTGGCCAACATAGTGAAAGCCCATCTCGACTAAAAATACAAAAA GGTCAGGAGTGCAAAACCAGCCTGGCCAACATGGTGAAAGCCCATCTCGACTAAAAATACAAAAA T C AC008764.1 Ensembl:ENSG00000141979 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs992341192 Functional Loss SNV dbSNP153 33..33 33 - - - 2159 RMVar_ID_2159 Human_SNP_ID_659927127 A-to-I Human chr19 - 16549031 16549031 16549031 GGCTCAAGTGATCCACCTGCCTTGGCTCCCATAGTGTTGGGATTACAGGTGTGAGCCACCGTGCC GGCTCAAGTGATCCACCTGCCTTGGCTCCCATTGTGTTGGGATTACAGGTGTGAGCCACCGTGCC T A AC008764.1 Ensembl:ENSG00000141979 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037027429 Functional Loss SNV dbSNP153 33..33 33 - - - 2160 RMVar_ID_2160 Human_SNP_ID_659927200 A-to-I Human chr19 - 16549315 16549315 16549315 TAAAGATGGAGTTTCACCTTGTTGCCCAGGCTAGTCTCAAACTCTGGGGCTCAAGCTATCTGGCC TAAAGATGGAGTTTCACCTTGTTGCCCAGGCTGGTCTCAAACTCTGGGGCTCAAGCTATCTGGCC T C AC008764.1 Ensembl:ENSG00000141979 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1313681882 Functional Loss SNV dbSNP153 33..33 33 - - - 2161 RMVar_ID_2161 Human_SNP_ID_659927220 A-to-I Human chr19 - 16549390 16549390 16549390 CCTTCCGCCTCAGCCTCCCAAGTAGCTGGGATACAGGCATGTGCCACCAAACCTGGCTAATTTTT CCTTCCGCCTCAGCCTCCCAAGTAGCTGGGATGCAGGCATGTGCCACCAAACCTGGCTAATTTTT T C AC008764.1 Ensembl:ENSG00000141979 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1328652874 Functional Loss SNV dbSNP153 33..33 33 - - - 2162 RMVar_ID_2162 Human_SNP_ID_659927226 A-to-I Human chr19 - 16549402 16549402 16549402 GACTCAAGGGATCCTTCCGCCTCAGCCTCCCAAGTAGCTGGGATACAGGCATGTGCCACCAAACC GACTCAAGGGATCCTTCCGCCTCAGCCTCCCAGGTAGCTGGGATACAGGCATGTGCCACCAAACC T C AC008764.1 Ensembl:ENSG00000141979 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1377074831 Functional Loss SNV dbSNP153 33..33 33 - - - 2163 RMVar_ID_2163 Human_SNP_ID_659927313 A-to-I Human chr19 - 16549667 16549667 16549667 TTTTTTCTTCTGAGCCAAAAATAAGGACGTGCAATTTGTGAATTGATTAGATGATACAATGAAAA TTTTTTCTTCTGAGCCAAAAATAAGGACGTGCTATTTGTGAATTGATTAGATGATACAATGAAAA T A AC008764.1 Ensembl:ENSG00000141979 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4808515 Functional Loss SNV dbSNP153 33..33 33 - - - 2164 RMVar_ID_2164 Human_SNP_ID_659927314 A-to-I Human chr19 - 16549667 16549667 16549667 TTTTTTCTTCTGAGCCAAAAATAAGGACGTGCAATTTGTGAATTGATTAGATGATACAATGAAAA TTTTTTCTTCTGAGCCAAAAATAAGGACGTGCGATTTGTGAATTGATTAGATGATACAATGAAAA T C AC008764.1 Ensembl:ENSG00000141979 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4808515 Functional Loss SNV dbSNP153 33..33 33 - - - 2165 RMVar_ID_2165 Human_SNP_ID_659927525 A-to-I Human chr19 - 16550468 16550468 16550468 CCTTGGCCTCCCAAAGTGCTAGGATGACAGGCATGAGCCACCGTGCCCAGCCTGATTGACAATGG CCTTGGCCTCCCAAAGTGCTAGGATGACAGGCCTGAGCCACCGTGCCCAGCCTGATTGACAATGG T G AC008764.1,SLC35E1 Ensembl:ENSG00000141979,Ensembl:ENSG00000127526 Protein coding,Protein coding intron,exon GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1344398884 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1974048 2166 RMVar_ID_2166 Human_SNP_ID_659927528 A-to-I Human chr19 - 16550480 16550480 16550480 ATGATCCGCCCACCTTGGCCTCCCAAAGTGCTAGGATGACAGGCATGAGCCACCGTGCCCAGCCT ATGATCCGCCCACCTTGGCCTCCCAAAGTGCTGGGATGACAGGCATGAGCCACCGTGCCCAGCCT T C AC008764.1,SLC35E1 Ensembl:ENSG00000141979,Ensembl:ENSG00000127526 Protein coding,Protein coding intron,intron GSE47997;GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 23474544,24183664,31158229,31158229 RNA-Seq:(High) rs1014331538 Functional Loss SNV dbSNP153 33..33 33 - - - 2167 RMVar_ID_2167 Human_SNP_ID_659927547 A-to-I Human chr19 - 16550551 16550551 16550551 ATTTTTTGTGTTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGG ATTTTTTGTGTTTTTAGTAGAGACAGGGTTTCGCCATGTTGGCCAGGCTGGTCTCGAACTCCTGG T C AC008764.1,SLC35E1 Ensembl:ENSG00000141979,Ensembl:ENSG00000127526 Protein coding,Protein coding intron,intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs537959580 Functional Loss SNV dbSNP153 33..33 33 - - - 2168 RMVar_ID_2168 Human_SNP_ID_659927564 A-to-I Human chr19 - 16550620 16550620 16550620 TCAGGTGATTCTCGTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCATGCACCACCACGGCTG TCAGGTGATTCTCGTGCCTCAGCCTCCCGAGTGGCTGGGATTACAGGCATGCACCACCACGGCTG T C AC008764.1,SLC35E1 Ensembl:ENSG00000141979,Ensembl:ENSG00000127526 Protein coding,Protein coding intron,intron GSE47997;GSE99789;GSE123020:GSM3490829,GSM3490830,GSM3490831 K562 cells&HepG2 cells;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109 cell line - 23474544,29796672,32596459 RNA-Seq:(High) rs1409983225 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_139998 2169 RMVar_ID_2169 Human_SNP_ID_659927896 A-to-I Human chr19 - 16551822 16551822 16551822 TGAGCCCAGGAGGTGGAGGTTTCAGCGAGCTGAGATCACACCACTGCACTCCAGCCTTGGTGACA TGAGCCCAGGAGGTGGAGGTTTCAGCGAGCTGGGATCACACCACTGCACTCCAGCCTTGGTGACA T C AC008764.1,SLC35E1 Ensembl:ENSG00000141979,Ensembl:ENSG00000127526 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1228185111 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1974070 2170 RMVar_ID_2170 Human_SNP_ID_659927900 A-to-I Human chr19 - 16551847 16551847 16551847 GGGAGGCTGAGGCAGGAGAATCACTTGAGCCCAGGAGGTGGAGGTTTCAGCGAGCTGAGATCACA GGGAGGCTGAGGCAGGAGAATCACTTGAGCCCGGGAGGTGGAGGTTTCAGCGAGCTGAGATCACA T C AC008764.1,SLC35E1 Ensembl:ENSG00000141979,Ensembl:ENSG00000127526 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941974239 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23785382,Human_RBP_ID_25388014 Human_Splice_Rec_1974070 2171 RMVar_ID_2171 Human_SNP_ID_659927924 A-to-I Human chr19 - 16551968 16551968 16551968 AGGCTGAGGTGGGTGGATCACTGGAGTTTGAGACCACCCTGGCCAACATGGTGAAACCCCATCTC AGGCTGAGGTGGGTGGATCACTGGAGTTTGAGGCCACCCTGGCCAACATGGTGAAACCCCATCTC T C AC008764.1,SLC35E1 Ensembl:ENSG00000141979,Ensembl:ENSG00000127526 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1169549303 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9084884,Human_RBP_ID_13387904 Human_miRNA_ID_1528700 2172 RMVar_ID_2172 Human_SNP_ID_659928043 A-to-I Human chr19 - 16552431 16552431 16552431 CCTCAGGCTGCTGAGGCAGGCGAATTGCTTGAACCTGGGAGGCAGAAGTTGTGGTGAGCCGAGAT CCTCAGGCTGCTGAGGCAGGCGAATTGCTTGAGCCTGGGAGGCAGAAGTTGTGGTGAGCCGAGAT T C AC008764.1,SLC35E1 Ensembl:ENSG00000141979,Ensembl:ENSG00000127526 Protein coding,Protein coding intron,3'UTR GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,29796672,31158229,32596459 RNA-Seq:(High) rs1005379191 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1462428 2173 RMVar_ID_2173 Human_SNP_ID_659928047 A-to-I Human chr19 - 16552459 16552459 16552459 ATGGTGTCGCGTGCCTGTAGTCCCAGCTCCTCAGGCTGCTGAGGCAGGCGAATTGCTTGAACCTG ATGGTGTCGCGTGCCTGTAGTCCCAGCTCCTCGGGCTGCTGAGGCAGGCGAATTGCTTGAACCTG T C AC008764.1,SLC35E1 Ensembl:ENSG00000141979,Ensembl:ENSG00000127526 Protein coding,Protein coding intron,3'UTR GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs543792206 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_515344,Human_RBP_ID_23785388,Human_RBP_ID_27464815 2174 RMVar_ID_2174 Human_SNP_ID_659929083 A-to-I Human chr19 - 16556033 16556033 16556033 TTTTGTATTTTTAATAGAGACACAGTTTTACCATGTTGGTCAGGCTGGTCTTGAACTCCTGACCT TTTTGTATTTTTAATAGAGACACAGTTTTACCGTGTTGGTCAGGCTGGTCTTGAACTCCTGACCT T C AC008764.1,SLC35E1 Ensembl:ENSG00000141979,Ensembl:ENSG00000127526 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1429466835 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12003,RMVar_hsa_circ_312140,RMVar_hsa_circ_193202 2175 RMVar_ID_2175 Human_SNP_ID_659929088 A-to-I Human chr19 - 16556052 16556052 16556052 CCACACCACACCCGACCAATTTTGTATTTTTAATAGAGACACAGTTTTACCATGTTGGTCAGGCT CCACACCACACCCGACCAATTTTGTATTTTTAGTAGAGACACAGTTTTACCATGTTGGTCAGGCT T C AC008764.1,SLC35E1 Ensembl:ENSG00000141979,Ensembl:ENSG00000127526 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264735916 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12003,RMVar_hsa_circ_312140,RMVar_hsa_circ_193202 2176 RMVar_ID_2176 Human_SNP_ID_659929155 A-to-I Human chr19 - 16556336 16556334 16556336 CCTGGCTAATTTTTTTTTTTTTTTGTAGAGACAGGGTCTCACTGTGTTGCCCAGGCTGCCCTCGA CCTGGCTAATTTTTTTTTTTTTTTGTAGAGAC__GGTCTCACTGTGTTGCCCAGGCTGCCCTCGA CCT C AC008764.1,SLC35E1 Ensembl:ENSG00000141979,Ensembl:ENSG00000127526 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941353060 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_12003,RMVar_hsa_circ_312140,RMVar_hsa_circ_193202 2177 RMVar_ID_2177 Human_SNP_ID_659929188 A-to-I Human chr19 - 16556426 16556426 16556426 TAGCTCACTGTAGCCTTGAACTCCTAGGCTCAAGCGATCCTCCCACCTCAGCCTCCCAGGTAGCT TAGCTCACTGTAGCCTTGAACTCCTAGGCTCAGGCGATCCTCCCACCTCAGCCTCCCAGGTAGCT T C AC008764.1,SLC35E1 Ensembl:ENSG00000141979,Ensembl:ENSG00000127526 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1051181720 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12003,RMVar_hsa_circ_312140,RMVar_hsa_circ_193202 2178 RMVar_ID_2178 Human_SNP_ID_659929201 A-to-I Human chr19 - 16556452 16556452 16556452 CAGGCTGGGGTGCTATGGCGCCATCGTAGCTCACTGTAGCCTTGAACTCCTAGGCTCAAGCGATC CAGGCTGGGGTGCTATGGCGCCATCGTAGCTCTCTGTAGCCTTGAACTCCTAGGCTCAAGCGATC T A AC008764.1,SLC35E1 Ensembl:ENSG00000141979,Ensembl:ENSG00000127526 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1324949930 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12003,RMVar_hsa_circ_312140,RMVar_hsa_circ_193202 2179 RMVar_ID_2179 Human_SNP_ID_659929208 A-to-I Human chr19 - 16556470 16556470 16556470 GTGTCTTACACTGTCGCCCAGGCTGGGGTGCTATGGCGCCATCGTAGCTCACTGTAGCCTTGAAC GTGTCTTACACTGTCGCCCAGGCTGGGGTGCTGTGGCGCCATCGTAGCTCACTGTAGCCTTGAAC T C AC008764.1,SLC35E1 Ensembl:ENSG00000141979,Ensembl:ENSG00000127526 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1337902775 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_771379,Human_RBP_ID_13387993 RMVar_hsa_circ_12003,RMVar_hsa_circ_312140,RMVar_hsa_circ_193202 2180 RMVar_ID_2180 Human_SNP_ID_659929770 A-to-I Human chr19 - 16558519 16558519 16558519 CAGCCTGCCCAATATAGTGAAACTCCTCCTCTACTAAAAATAGAAAAATTAGCCAGGTGTGGTGC CAGCCTGCCCAATATAGTGAAACTCCTCCTCTCCTAAAAATAGAAAAATTAGCCAGGTGTGGTGC T G AC008764.1,SLC35E1 Ensembl:ENSG00000141979,Ensembl:ENSG00000127526 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs567481455 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12003,RMVar_hsa_circ_312140,RMVar_hsa_circ_193202 2181 RMVar_ID_2181 Human_SNP_ID_659929778 A-to-I Human chr19 - 16558536 16558536 16558536 GGTCAGGAGTTCGAGACCAGCCTGCCCAATATAGTGAAACTCCTCCTCTACTAAAAATAGAAAAA GGTCAGGAGTTCGAGACCAGCCTGCCCAATATGGTGAAACTCCTCCTCTACTAAAAATAGAAAAA T C AC008764.1,SLC35E1 Ensembl:ENSG00000141979,Ensembl:ENSG00000127526 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1369604674 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12003,RMVar_hsa_circ_312140,RMVar_hsa_circ_193202 2182 RMVar_ID_2182 Human_SNP_ID_659929798 A-to-I Human chr19 - 16558583 16558583 16558583 AATCCAATCCCAGCACTTTGGAAGGCCGAGCCAGGTGGATCACTTGAGGTCAGGAGTTCGAGACC AATCCAATCCCAGCACTTTGGAAGGCCGAGCCCGGTGGATCACTTGAGGTCAGGAGTTCGAGACC T G AC008764.1,SLC35E1 Ensembl:ENSG00000141979,Ensembl:ENSG00000127526 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1490911931 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12003,RMVar_hsa_circ_312140,RMVar_hsa_circ_193202 2183 RMVar_ID_2183 Human_SNP_ID_659930017 A-to-I Human chr19 - 16559385 16559384 16559385 AAACTTCTGGGCTTAAGTGATCCACCCGCCTCAGCCTCCCAAAGTGCTGGGACTATAGACATGAG AAACTTCTGGGCTTAAGTGATCCACCCGCCTC_GCCTCCCAAAGTGCTGGGACTATAGACATGAG CT C AC008764.1,SLC35E1 Ensembl:ENSG00000141979,Ensembl:ENSG00000127526 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs368769774 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_12003,RMVar_hsa_circ_312140,RMVar_hsa_circ_193202 2184 RMVar_ID_2184 Human_SNP_ID_659930226 A-to-I Human chr19 - 16560084 16560084 16560084 AGAGACCACCGCTTGGCTTTCAGACTGACCACAGGCGGCACAGACTCAGGACAGAGCCAAATACC AGAGACCACCGCTTGGCTTTCAGACTGACCACTGGCGGCACAGACTCAGGACAGAGCCAAATACC T A AC008764.1,SLC35E1 Ensembl:ENSG00000141979,Ensembl:ENSG00000127526 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6512120 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22358940,Human_RBP_ID_26337650 GWAS_ID_10,GWAS_ID_11,GWAS_ID_12,GWAS_ID_13 RMVar_hsa_circ_12003,RMVar_hsa_circ_312140,RMVar_hsa_circ_193202 2185 RMVar_ID_2185 Human_SNP_ID_659930227 A-to-I Human chr19 - 16560084 16560084 16560084 AGAGACCACCGCTTGGCTTTCAGACTGACCACAGGCGGCACAGACTCAGGACAGAGCCAAATACC AGAGACCACCGCTTGGCTTTCAGACTGACCACGGGCGGCACAGACTCAGGACAGAGCCAAATACC T C AC008764.1,SLC35E1 Ensembl:ENSG00000141979,Ensembl:ENSG00000127526 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6512120 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22358940,Human_RBP_ID_26337650 GWAS_ID_10,GWAS_ID_11,GWAS_ID_12,GWAS_ID_13 RMVar_hsa_circ_12003,RMVar_hsa_circ_312140,RMVar_hsa_circ_193202 2186 RMVar_ID_2186 Human_SNP_ID_659931046 A-to-I Human chr19 - 16562837 16562837 16562837 CGGCATGGTGGCACATGCCTGTAGTCCGAGCTACTTGGGAGCCTGAGGTGGGAAGATCACTTGAG CGGCATGGTGGCACATGCCTGTAGTCCGAGCTGCTTGGGAGCCTGAGGTGGGAAGATCACTTGAG T C AC008764.1,SLC35E1 Ensembl:ENSG00000141979,Ensembl:ENSG00000127526 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs999697104 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8479141,Human_RBP_ID_25388045 RMVar_hsa_circ_12003,RMVar_hsa_circ_312140,RMVar_hsa_circ_193202 2187 RMVar_ID_2187 Human_SNP_ID_659931087 A-to-I Human chr19 - 16562993 16562993 16562993 TTTAAATTTACAGGTCAGGCACAGTGCCTCACACATGTAATCCCAGTATTTTGGAAGGCAGAGGC TTTAAATTTACAGGTCAGGCACAGTGCCTCACCCATGTAATCCCAGTATTTTGGAAGGCAGAGGC T G AC008764.1,SLC35E1 Ensembl:ENSG00000141979,Ensembl:ENSG00000127526 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs902186639 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17567978 RMVar_hsa_circ_12003,RMVar_hsa_circ_312140,RMVar_hsa_circ_193202 2188 RMVar_ID_2188 Human_SNP_ID_659931121 A-to-I Human chr19 - 16563118 16563118 16563118 TGGGGTTTCTCCATTTTGGCCAGGCTAGTCTCAAACTCCTGACATTAGGTGATCCACCCACTTCG TGGGGTTTCTCCATTTTGGCCAGGCTAGTCTCGAACTCCTGACATTAGGTGATCCACCCACTTCG T C AC008764.1,SLC35E1 Ensembl:ENSG00000141979,Ensembl:ENSG00000127526 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs898544596 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12003,RMVar_hsa_circ_312140,RMVar_hsa_circ_193202 2189 RMVar_ID_2189 Human_SNP_ID_659931122 A-to-I Human chr19 - 16563124 16563124 16563124 TAGAGGTGGGGTTTCTCCATTTTGGCCAGGCTAGTCTCAAACTCCTGACATTAGGTGATCCACCC TAGAGGTGGGGTTTCTCCATTTTGGCCAGGCTGGTCTCAAACTCCTGACATTAGGTGATCCACCC T C AC008764.1,SLC35E1 Ensembl:ENSG00000141979,Ensembl:ENSG00000127526 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1013023514 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12003,RMVar_hsa_circ_312140,RMVar_hsa_circ_193202 2190 RMVar_ID_2190 Human_SNP_ID_659931124 A-to-I Human chr19 - 16563138 16563138 16563138 TTGTGTGTTTTTACTAGAGGTGGGGTTTCTCCATTTTGGCCAGGCTAGTCTCAAACTCCTGACAT TTGTGTGTTTTTACTAGAGGTGGGGTTTCTCCTTTTTGGCCAGGCTAGTCTCAAACTCCTGACAT T A AC008764.1,SLC35E1 Ensembl:ENSG00000141979,Ensembl:ENSG00000127526 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1023078006 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12003,RMVar_hsa_circ_312140,RMVar_hsa_circ_193202 2191 RMVar_ID_2191 Human_SNP_ID_659931163 A-to-I Human chr19 - 16563293 16563293 16563293 TTTTGAGACGGAGTTTTTCTGTCTCCTAGGCTAGAATGCAATGGCATGTTCTCGGCTCACTGCAG TTTTGAGACGGAGTTTTTCTGTCTCCTAGGCTGGAATGCAATGGCATGTTCTCGGCTCACTGCAG T C AC008764.1,SLC35E1 Ensembl:ENSG00000141979,Ensembl:ENSG00000127526 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs898325066 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12003,RMVar_hsa_circ_312140,RMVar_hsa_circ_193202 2192 RMVar_ID_2192 Human_SNP_ID_659931266 A-to-I Human chr19 - 16563622 16563622 16563622 ATAAAAATTATCTGGTGTGGTGGCGTACGCCTATAATCCTAGCTACTAGGTAGGTGGAGGTTGCA ATAAAAATTATCTGGTGTGGTGGCGTACGCCTCTAATCCTAGCTACTAGGTAGGTGGAGGTTGCA T G AC008764.1,SLC35E1 Ensembl:ENSG00000141979,Ensembl:ENSG00000127526 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs113899774 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_515368,Human_RBP_ID_22809731,Human_RBP_ID_23785414 RMVar_hsa_circ_12003,RMVar_hsa_circ_312140,RMVar_hsa_circ_193202 2193 RMVar_ID_2193 Human_SNP_ID_659931518 A-to-I Human chr19 - 16564578 16564578 16564578 GTCTTGGCCAGGCGCAGTGGCTCCAGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGCAGA GTCTTGGCCAGGCGCAGTGGCTCCAGCCTGTACTCCCAGCACTTTGGGAGGCCGAGGTGGGCAGA T G AC008764.1,SLC35E1 Ensembl:ENSG00000141979,Ensembl:ENSG00000127526 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1273184370 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12003,RMVar_hsa_circ_312140,RMVar_hsa_circ_193202 2194 RMVar_ID_2194 Human_SNP_ID_659931769 A-to-I Human chr19 - 16565485 16565485 16565485 CATGCGCTGCCTGGGTGTGGTGGCTTACGCCTATAATCCCAGCACTTTGGGAGGCCAAGGTGTGT CATGCGCTGCCTGGGTGTGGTGGCTTACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGTGT T C AC008764.1,SLC35E1 Ensembl:ENSG00000141979,Ensembl:ENSG00000127526 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs545099132 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193203,RMVar_hsa_circ_12003,RMVar_hsa_circ_312140,RMVar_hsa_circ_193202,RMVar_hsa_circ_323985 2195 RMVar_ID_2195 Human_SNP_ID_659931782 A-to-I Human chr19 - 16565516 16565515 16565516 GAGACTCCGTGTCAAAAAAAAAAGAAAAAAACATGCGCTGCCTGGGTGTGGTGGCTTACGCCTAT GAGACTCCGTGTCAAAAAAAAAAGAAAAAAAC_TGCGCTGCCTGGGTGTGGTGGCTTACGCCTAT AT A AC008764.1,SLC35E1 Ensembl:ENSG00000141979,Ensembl:ENSG00000127526 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1183649842 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_193203,RMVar_hsa_circ_12003,RMVar_hsa_circ_312140,RMVar_hsa_circ_193202,RMVar_hsa_circ_323985 2196 RMVar_ID_2196 Human_SNP_ID_659931783 A-to-I Human chr19 - 16565516 16565516 16565516 GAGACTCCGTGTCAAAAAAAAAAGAAAAAAACATGCGCTGCCTGGGTGTGGTGGCTTACGCCTAT GAGACTCCGTGTCAAAAAAAAAAGAAAAAAACGTGCGCTGCCTGGGTGTGGTGGCTTACGCCTAT T C AC008764.1,SLC35E1 Ensembl:ENSG00000141979,Ensembl:ENSG00000127526 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10413178 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_14,GWAS_ID_15,GWAS_ID_16,GWAS_ID_17 RMVar_hsa_circ_193203,RMVar_hsa_circ_12003,RMVar_hsa_circ_312140,RMVar_hsa_circ_193202,RMVar_hsa_circ_323985 2197 RMVar_ID_2197 Human_SNP_ID_659931920 A-to-I Human chr19 - 16565910 16565910 16565910 CCTGGCGTTAAGAGATCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGATGTGAGCCACTGTGC CCTGGCGTTAAGAGATCTGCCTTGGCCTCCCAGAGTGCTGGGATTACAGATGTGAGCCACTGTGC T C AC008764.1,SLC35E1 Ensembl:ENSG00000141979,Ensembl:ENSG00000127526 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1216300502 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193203,RMVar_hsa_circ_12003,RMVar_hsa_circ_312140,RMVar_hsa_circ_193202,RMVar_hsa_circ_323985 2198 RMVar_ID_2198 Human_SNP_ID_659931981 A-to-I Human chr19 - 16566168 16566168 16566168 TTTTTTATTTTAAATGTTTATTTTTTAGAGACAGAACCTCGCTCTGTTGCCAGGGCTGGAGTGCA TTTTTTATTTTAAATGTTTATTTTTTAGAGACGGAACCTCGCTCTGTTGCCAGGGCTGGAGTGCA T C AC008764.1,SLC35E1 Ensembl:ENSG00000141979,Ensembl:ENSG00000127526 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1466718528 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2558472 RMVar_hsa_circ_193203,RMVar_hsa_circ_12003,RMVar_hsa_circ_312140,RMVar_hsa_circ_193202,RMVar_hsa_circ_323985 2199 RMVar_ID_2199 Human_SNP_ID_659932629 A-to-I Human chr19 - 16568616 16568616 16568616 TGAGGCAGGAGAATCGCTTGAACCCGGGAAGCAGAGGTTGCAGTGAGCCACGATTGTGCCACTAC TGAGGCAGGAGAATCGCTTGAACCCGGGAAGCCGAGGTTGCAGTGAGCCACGATTGTGCCACTAC T G AC008764.1,SLC35E1 Ensembl:ENSG00000141979,Ensembl:ENSG00000127526 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1416151495 Functional Loss SNV dbSNP153 33..33 33 - - - 2200 RMVar_ID_2200 Human_SNP_ID_659932757 A-to-I Human chr19 - 16569149 16569149 16569149 GTGGTGGTAGGCACCTGTAGTCCCAGCTACTCAGAAAGCTGAGGCAGAAGAATCGGTTGAACCTG GTGGTGGTAGGCACCTGTAGTCCCAGCTACTCGGAAAGCTGAGGCAGAAGAATCGGTTGAACCTG T C AC008764.1,SLC35E1 Ensembl:ENSG00000141979,Ensembl:ENSG00000127526 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs542877583 Functional Loss SNV dbSNP153 33..33 33 - - - 2201 RMVar_ID_2201 Human_SNP_ID_659932881 A-to-I Human chr19 - 16569666 16569666 16569666 AATTTTTGTATTTTCAATACAGACAGGGTTTTACCATGTTGGCCAGGCTGGTCTCAAACTCCTGA AATTTTTGTATTTTCAATACAGACAGGGTTTTGCCATGTTGGCCAGGCTGGTCTCAAACTCCTGA T C AC008764.1,SLC35E1 Ensembl:ENSG00000141979,Ensembl:ENSG00000127526 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs981026416 Functional Loss SNV dbSNP153 33..33 33 - - - 2202 RMVar_ID_2202 Human_SNP_ID_659932887 A-to-I Human chr19 - 16569683 16569683 16569683 TTCCATCACTCCTGGCTAATTTTTGTATTTTCAATACAGACAGGGTTTTACCATGTTGGCCAGGC TTCCATCACTCCTGGCTAATTTTTGTATTTTCGATACAGACAGGGTTTTACCATGTTGGCCAGGC T C AC008764.1,SLC35E1 Ensembl:ENSG00000141979,Ensembl:ENSG00000127526 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs919995971 Functional Loss SNV dbSNP153 33..33 33 - - - 2203 RMVar_ID_2203 Human_SNP_ID_659932898 A-to-I Human chr19 - 16569734 16569734 16569734 GTTCAAGCGATTCTTGCCTCAGCCTCCCGAGTAGCCGGGATTGCAGGCGCGTTCCATCACTCCTG GTTCAAGCGATTCTTGCCTCAGCCTCCCGAGTGGCCGGGATTGCAGGCGCGTTCCATCACTCCTG T C AC008764.1,SLC35E1 Ensembl:ENSG00000141979,Ensembl:ENSG00000127526 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1374444543 Functional Loss SNV dbSNP153 33..33 33 - - - 2204 RMVar_ID_2204 Human_SNP_ID_659932919 A-to-I Human chr19 - 16569792 16569792 16569792 TTGCCCAGATTGGAGTGCCGTGGTGCGATCTCAGCTTACTGCAAGCTCCGCCTCCTGGGTTCAAG TTGCCCAGATTGGAGTGCCGTGGTGCGATCTCGGCTTACTGCAAGCTCCGCCTCCTGGGTTCAAG T C AC008764.1,SLC35E1 Ensembl:ENSG00000141979,Ensembl:ENSG00000127526 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1244821924 Functional Loss SNV dbSNP153 33..33 33 - - - 2205 RMVar_ID_2205 Human_SNP_ID_659933533 A-to-I Human chr19 - 16572042 16572042 16572042 GTCGTCCGGCCCGCTGCTGCCGCCGCGCTTCTACCCGCGCTACGTGCTACCGCTCGCCTTCGGCA GTCGTCCGGCCCGCTGCTGCCGCCGCGCTTCTCCCCGCGCTACGTGCTACCGCTCGCCTTCGGCA T G AC008764.1,SLC35E1 Ensembl:ENSG00000141979,Ensembl:ENSG00000127526 Protein coding,Protein coding intron,CDS GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs764959391 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241514,Human_RBP_ID_515372,Human_RBP_ID_4557308,Human_RBP_ID_8255840,Human_RBP_ID_9328754 Human_Splice_Rec_1974049,Human_Splice_Rec_1974071,Human_Splice_Rec_1974091 2206 RMVar_ID_2206 Human_SNP_ID_659944407 A-to-I Human chr19 - 16614407 16614407 16614407 CTCCTACCTCAGCCTTCTGAGTAGCTAAGACTACAGACACACGCTACCACACCCAGCTAATTTTT CTCCTACCTCAGCCTTCTGAGTAGCTAAGACTGCAGACACACGCTACCACACCCAGCTAATTTTT T C AC008764.4,AC008764.1,MED26 Ensembl:ENSG00000268790,Ensembl:ENSG00000141979,Ensembl:ENSG00000105085 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs762171659 Functional Loss SNV dbSNP153 33..33 33 - - - 2207 RMVar_ID_2207 Human_SNP_ID_659948803 A-to-I Human chr19 - 16631166 16631166 16631166 GGCCAGGCTGGTCTCTTAACTCCTTACCTCAAATGATCCACCCACCTCGGCCTCCCAAAGTGCTG GGCCAGGCTGGTCTCTTAACTCCTTACCTCAAGTGATCCACCCACCTCGGCCTCCCAAAGTGCTG T C SMIM7,AC008764.4 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 Protein coding,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1358312684 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6725533,Human_RBP_ID_17916680 Human_Splice_Rec_1974200 RMVar_hsa_circ_349256 2208 RMVar_ID_2208 Human_SNP_ID_659948804 A-to-I Human chr19 - 16631167 16631167 16631167 TGGCCAGGCTGGTCTCTTAACTCCTTACCTCAAATGATCCACCCACCTCGGCCTCCCAAAGTGCT TGGCCAGGCTGGTCTCTTAACTCCTTACCTCAGATGATCCACCCACCTCGGCCTCCCAAAGTGCT T C SMIM7,AC008764.4 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 Protein coding,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1298716391 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6725533,Human_RBP_ID_17916680 Human_Splice_Rec_1974200 RMVar_hsa_circ_349256 2209 RMVar_ID_2209 Human_SNP_ID_659949269 A-to-I Human chr19 - 16632887 16632887 16632887 CTTCAGATAAACTTTTAGAAGTTGTGAATTTCAGTACGCTCATATCCACAGGGTCAGAGGGTATG CTTCAGATAAACTTTTAGAAGTTGTGAATTTCGGTACGCTCATATCCACAGGGTCAGAGGGTATG T C SMIM7,AC008764.4 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs527441342 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_349256 2210 RMVar_ID_2210 Human_SNP_ID_659949676 A-to-I Human chr19 - 16634559 16634559 16634559 TTGGCTACGCTGGTCTCAAACTCCTGAGCTCAAGTGACCCGCCTACCTCAGCCTTTCAAAGTGCT TTGGCTACGCTGGTCTCAAACTCCTGAGCTCAGGTGACCCGCCTACCTCAGCCTTTCAAAGTGCT T C AC024075.2,SMIM7,AC008764.4 Ensembl:ENSG00000269044,Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 lincRNA,Protein coding,Protein coding exon,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs368212459 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3589584 RMVar_hsa_circ_349256 2211 RMVar_ID_2211 Human_SNP_ID_659949677 A-to-I Human chr19 - 16634559 16634559 16634559 TTGGCTACGCTGGTCTCAAACTCCTGAGCTCAAGTGACCCGCCTACCTCAGCCTTTCAAAGTGCT TTGGCTACGCTGGTCTCAAACTCCTGAGCTCACGTGACCCGCCTACCTCAGCCTTTCAAAGTGCT T G AC024075.2,SMIM7,AC008764.4 Ensembl:ENSG00000269044,Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 lincRNA,Protein coding,Protein coding exon,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs368212459 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3589584 RMVar_hsa_circ_349256 2212 RMVar_ID_2212 Human_SNP_ID_659949691 A-to-I Human chr19 - 16634605 16634605 16634605 CCTCCCTAATTTTTTGTATTTTTAGTACAGACAGGGTTTTGCCATGTTGGCTACGCTGGTCTCAA CCTCCCTAATTTTTTGTATTTTTAGTACAGACGGGGTTTTGCCATGTTGGCTACGCTGGTCTCAA T C AC024075.2,SMIM7,AC008764.4 Ensembl:ENSG00000269044,Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 lincRNA,Protein coding,Protein coding exon,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1466055909 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3589584 RMVar_hsa_circ_349256 2213 RMVar_ID_2213 Human_SNP_ID_659949693 A-to-I Human chr19 - 16634611 16634611 16634611 ACCACACCTCCCTAATTTTTTGTATTTTTAGTACAGACAGGGTTTTGCCATGTTGGCTACGCTGG ACCACACCTCCCTAATTTTTTGTATTTTTAGTGCAGACAGGGTTTTGCCATGTTGGCTACGCTGG T C AC024075.2,SMIM7,AC008764.4 Ensembl:ENSG00000269044,Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 lincRNA,Protein coding,Protein coding exon,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1172888453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3589584 RMVar_hsa_circ_349256 2214 RMVar_ID_2214 Human_SNP_ID_659949705 A-to-I Human chr19 - 16634661 16634661 16634661 TGGTTCTCCTACCTCAGCCTCCCAAATAGCTGAGACTCCAGGCATCCACCACCACACCTCCCTAA TGGTTCTCCTACCTCAGCCTCCCAAATAGCTGGGACTCCAGGCATCCACCACCACACCTCCCTAA T C AC024075.2,SMIM7,AC008764.4 Ensembl:ENSG00000269044,Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 lincRNA,Protein coding,Protein coding exon,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs977493064 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6725551,Human_RBP_ID_13388903 RMVar_hsa_circ_349256 2215 RMVar_ID_2215 Human_SNP_ID_659949706 A-to-I Human chr19 - 16634669 16634669 16634669 GATTCAAGTGGTTCTCCTACCTCAGCCTCCCAAATAGCTGAGACTCCAGGCATCCACCACCACAC GATTCAAGTGGTTCTCCTACCTCAGCCTCCCAGATAGCTGAGACTCCAGGCATCCACCACCACAC T C AC024075.2,SMIM7,AC008764.4 Ensembl:ENSG00000269044,Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 lincRNA,Protein coding,Protein coding exon,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs549924860 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13388903 RMVar_hsa_circ_349256 2216 RMVar_ID_2216 Human_SNP_ID_659949716 A-to-I Human chr19 - 16634709 16634709 16634709 CAGTGGCACGATCTTGGCTTACTGCAACCTCCACCTCCTGGATTCAAGTGGTTCTCCTACCTCAG CAGTGGCACGATCTTGGCTTACTGCAACCTCCGCCTCCTGGATTCAAGTGGTTCTCCTACCTCAG T C AC024075.2,SMIM7,AC008764.4 Ensembl:ENSG00000269044,Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 lincRNA,Protein coding,Protein coding exon,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1312062525 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_349256 2217 RMVar_ID_2217 Human_SNP_ID_659950015 A-to-I Human chr19 - 16635760 16635760 16635760 CCTGCCTCAGCTTCCCAAGTAGCTGGGATTACAGGCGCCTGCCACCAGGCCCAGCTAAATTTTTT CCTGCCTCAGCTTCCCAAGTAGCTGGGATTACGGGCGCCTGCCACCAGGCCCAGCTAAATTTTTT T C SMIM7,AC008764.4 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1423458344 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_349256 2218 RMVar_ID_2218 Human_SNP_ID_659950036 A-to-I Human chr19 - 16635837 16635837 16635837 CTCTGTTGCCCAGGCTGGATTGCAGTGGTACAATCTGGGCCCATTGCAACCTCTCCCTCCCAGGT CTCTGTTGCCCAGGCTGGATTGCAGTGGTACAGTCTGGGCCCATTGCAACCTCTCCCTCCCAGGT T C SMIM7,AC008764.4 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs902752708 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_349256 2219 RMVar_ID_2219 Human_SNP_ID_659950319 A-to-I Human chr19 - 16636701 16636701 16636701 GCAGTCCTCCCACCTCAGCCTCCCAAAGTGCCAGGATTATAGGCATGGGCCATTGTGCCTGGCTA GCAGTCCTCCCACCTCAGCCTCCCAAAGTGCCTGGATTATAGGCATGGGCCATTGTGCCTGGCTA T A SMIM7,AC008764.4 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 Protein coding,Protein coding intron,intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1479855228 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_349256 2220 RMVar_ID_2220 Human_SNP_ID_659950451 A-to-I Human chr19 - 16637391 16637391 16637391 AAGCGATCCTCCCACCTCAGCCTCCTGGGACTACAGGCACATACCACCACAGCTGGCTAATGTAT AAGCGATCCTCCCACCTCAGCCTCCTGGGACTGCAGGCACATACCACCACAGCTGGCTAATGTAT T C SMIM7,AC008764.4 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 Protein coding,Protein coding intron,intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1211561877 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_349256 2221 RMVar_ID_2221 Human_SNP_ID_659950637 A-to-I Human chr19 - 16638215 16638215 16638215 TCATCCAGGCTGGAGTGCAGTGGCGTGATCCCAGCTTACTGCAACCTCCGCCTCCGGCTTTAAGT TCATCCAGGCTGGAGTGCAGTGGCGTGATCCCCGCTTACTGCAACCTCCGCCTCCGGCTTTAAGT T G SMIM7,AC008764.4 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054401155 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_349256 2222 RMVar_ID_2222 Human_SNP_ID_659950724 A-to-I Human chr19 - 16638409 16638409 16638409 AATCCAGCTACTCAGGAGTCTGAGGCAGGAAAATCACCTGAACCCGGGAGGCAGGGGTTGCAGTG AATCCAGCTACTCAGGAGTCTGAGGCAGGAAAGTCACCTGAACCCGGGAGGCAGGGGTTGCAGTG T C SMIM7,AC008764.4 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs957998509 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_349256 2223 RMVar_ID_2223 Human_SNP_ID_659950726 A-to-I Human chr19 - 16638415 16638415 16638415 CCTGTAAATCCAGCTACTCAGGAGTCTGAGGCAGGAAAATCACCTGAACCCGGGAGGCAGGGGTT CCTGTAAATCCAGCTACTCAGGAGTCTGAGGCTGGAAAATCACCTGAACCCGGGAGGCAGGGGTT T A SMIM7,AC008764.4 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1010075759 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25388124 RMVar_hsa_circ_349256 2224 RMVar_ID_2224 Human_SNP_ID_659950730 A-to-I Human chr19 - 16638428 16638428 16638428 ATGGTGGCGGGCACCTGTAAATCCAGCTACTCAGGAGTCTGAGGCAGGAAAATCACCTGAACCCG ATGGTGGCGGGCACCTGTAAATCCAGCTACTCGGGAGTCTGAGGCAGGAAAATCACCTGAACCCG T C SMIM7,AC008764.4 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1020999548 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_349256 2225 RMVar_ID_2225 Human_SNP_ID_659950772 A-to-I Human chr19 - 16638574 16638574 16638574 GCCAGGCACGGTGGCTCATGCCTGTAATCCCAACACTTAGGGAGGCTGAGGTGGGTGGATCACCT GCCAGGCACGGTGGCTCATGCCTGTAATCCCAGCACTTAGGGAGGCTGAGGTGGGTGGATCACCT T C SMIM7,AC008764.4 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1007496025 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_349256 2226 RMVar_ID_2226 Human_SNP_ID_659950773 A-to-I Human chr19 - 16638581 16638581 16638581 GTTAATGGCCAGGCACGGTGGCTCATGCCTGTAATCCCAACACTTAGGGAGGCTGAGGTGGGTGG GTTAATGGCCAGGCACGGTGGCTCATGCCTGTGATCCCAACACTTAGGGAGGCTGAGGTGGGTGG T C SMIM7,AC008764.4 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs543844538 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_349256 2227 RMVar_ID_2227 Human_SNP_ID_659951258 A-to-I Human chr19 - 16640164 16640164 16640164 GCTGACAGGAGAATCGCTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCAGAGATCGTGCTGCTGC GCTGACAGGAGAATCGCTTGAACCTGGGAGGCCGAGGTTGCAGTGAGCAGAGATCGTGCTGCTGC T G SMIM7,AC008764.4,AC024075.1 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790,Ensembl:ENSG00000267904 Protein coding,Protein coding,lincRNA intron,intron,exon GSE38233;GSE100210;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 24183664,29129909,30559470 RNA-Seq:(High) rs1231232758 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_349256 2228 RMVar_ID_2228 Human_SNP_ID_659951281 A-to-I Human chr19 - 16640278 16640278 16640278 AATCCCAGAAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAA AATCCCAGAAGTTCGAGACCAGCCTGGCCAACGTGGTGAAACCCCATCTCTACTAAAAATACAAA T C SMIM7,AC008764.4,AC024075.1 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790,Ensembl:ENSG00000267904 Protein coding,Protein coding,lincRNA intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1043565101 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_349256 2229 RMVar_ID_2229 Human_SNP_ID_659951283 A-to-I Human chr19 - 16640280 16640280 16640280 GTAATCCCAGAAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACA GTAATCCCAGAAGTTCGAGACCAGCCTGGCCAGCATGGTGAAACCCCATCTCTACTAAAAATACA T C SMIM7,AC008764.4,AC024075.1 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790,Ensembl:ENSG00000267904 Protein coding,Protein coding,lincRNA intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs903599101 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_349256 2230 RMVar_ID_2230 Human_SNP_ID_659951395 A-to-I Human chr19 - 16640776 16640776 16640776 GGCACCCACCACCACGCCTGGATAATGTTGGTATTTTTAGTAGAGATGGGGTTTCTCCATGTTGG GGCACCCACCACCACGCCTGGATAATGTTGGTGTTTTTAGTAGAGATGGGGTTTCTCCATGTTGG T C SMIM7,AC008764.4 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886915197 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_349256 2231 RMVar_ID_2231 Human_SNP_ID_659951404 A-to-I Human chr19 - 16640833 16640833 16640833 CGCCTCCCGGGTTCAAGCGATTTTCTTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCACCCA CGCCTCCCGGGTTCAAGCGATTTTCTTGCCTCGGCCTCCCAAGTAGCTGGGACTACAGGCACCCA T C SMIM7,AC008764.4 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs899750426 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_349256 2232 RMVar_ID_2232 Human_SNP_ID_659951416 A-to-I Human chr19 - 16640886 16640886 16640886 CTCTGTCACCCAGGCTGGAGTGCAGTGGCGCAATCTCAGCTCACTGCAGCCTCCGCCTCCCGGGT CTCTGTCACCCAGGCTGGAGTGCAGTGGCGCAGTCTCAGCTCACTGCAGCCTCCGCCTCCCGGGT T C SMIM7,AC008764.4 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 Protein coding,Protein coding intron,intron GSE38233;GSE100210;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 24183664,29129909,30559470 RNA-Seq:(High) rs888054570 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_349256 2233 RMVar_ID_2233 Human_SNP_ID_659951551 A-to-I Human chr19 - 16641436 16641436 16641436 AAATTAGCCGAGTGTGGTGGTACAGGCCTGTAATCCCAGTTACTAGGGAGGCTGAGGCAGGAGAA AAATTAGCCGAGTGTGGTGGTACAGGCCTGTATTCCCAGTTACTAGGGAGGCTGAGGCAGGAGAA T A SMIM7,AC008764.4 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1210980849 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1974254 RMVar_hsa_circ_349256 2234 RMVar_ID_2234 Human_SNP_ID_659951627 A-to-I Human chr19 - 16641691 16641691 16641691 AGGAGGCTGAGGCAGGAGAATTGCTTGAACCCAGGAGGTGGAGGTTGCAGTGAGCCGAGATTTTT AGGAGGCTGAGGCAGGAGAATTGCTTGAACCCCGGAGGTGGAGGTTGCAGTGAGCCGAGATTTTT T G SMIM7,AC008764.4 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 Protein coding,Protein coding intron,intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1006912500 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_349256 2235 RMVar_ID_2235 Human_SNP_ID_659951628 A-to-I Human chr19 - 16641695 16641695 16641695 ACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAACCCAGGAGGTGGAGGTTGCAGTGAGCCGAGAT ACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAGCCCAGGAGGTGGAGGTTGCAGTGAGCCGAGAT T C SMIM7,AC008764.4 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 Protein coding,Protein coding intron,intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs565147149 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_349256 2236 RMVar_ID_2236 Human_SNP_ID_659951634 A-to-I Human chr19 - 16641723 16641723 16641723 GTCGTGCTGCACGCTTATAGTCCAAGCTACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAACCCA GTCGTGCTGCACGCTTATAGTCCAAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCTTGAACCCA T C SMIM7,AC008764.4 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs557149326 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_349256 2237 RMVar_ID_2237 Human_SNP_ID_659951636 A-to-I Human chr19 - 16641731 16641731 16641731 AGCCGGGTGTCGTGCTGCACGCTTATAGTCCAAGCTACTCAGGAGGCTGAGGCAGGAGAATTGCT AGCCGGGTGTCGTGCTGCACGCTTATAGTCCAGGCTACTCAGGAGGCTGAGGCAGGAGAATTGCT T C SMIM7,AC008764.4 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs577186562 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13389052 RMVar_hsa_circ_349256 2238 RMVar_ID_2238 Human_SNP_ID_659951638 A-to-I Human chr19 - 16641737 16641737 16641737 AAAACTAGCCGGGTGTCGTGCTGCACGCTTATAGTCCAAGCTACTCAGGAGGCTGAGGCAGGAGA AAAACTAGCCGGGTGTCGTGCTGCACGCTTATGGTCCAAGCTACTCAGGAGGCTGAGGCAGGAGA T C SMIM7,AC008764.4 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs545864173 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13389052 RMVar_hsa_circ_349256 2239 RMVar_ID_2239 Human_SNP_ID_659951640 A-to-I Human chr19 - 16641739 16641739 16641739 CAAAAACTAGCCGGGTGTCGTGCTGCACGCTTATAGTCCAAGCTACTCAGGAGGCTGAGGCAGGA CAAAAACTAGCCGGGTGTCGTGCTGCACGCTTGTAGTCCAAGCTACTCAGGAGGCTGAGGCAGGA T C SMIM7,AC008764.4 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978617039 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13389052 RMVar_hsa_circ_349256 2240 RMVar_ID_2240 Human_SNP_ID_659951826 A-to-I Human chr19 - 16642464 16642464 16642464 TTCACTGCAACCTCCACCTCCCAGGTTCAAGCAATTCTCATGCCTCAGCCTCCTGAATAGCTGGG TTCACTGCAACCTCCACCTCCCAGGTTCAAGCGATTCTCATGCCTCAGCCTCCTGAATAGCTGGG T C SMIM7,AC008764.4 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1207326783 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_349256 2241 RMVar_ID_2241 Human_SNP_ID_659951830 A-to-I Human chr19 - 16642487 16642487 16642487 GGAGTGCGGTGGTGTGATCTTGGTTCACTGCAACCTCCACCTCCCAGGTTCAAGCAATTCTCATG GGAGTGCGGTGGTGTGATCTTGGTTCACTGCATCCTCCACCTCCCAGGTTCAAGCAATTCTCATG T A SMIM7,AC008764.4 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 Protein coding,Protein coding intron,intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1235236976 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_349256 2242 RMVar_ID_2242 Human_SNP_ID_659951887 A-to-I Human chr19 - 16642728 16642728 16642728 ACGATCCTCCCACCTCAGTCTCCCAAGTACCTAGGACCACAGGCATGTACCACAGGCTAATTATT ACGATCCTCCCACCTCAGTCTCCCAAGTACCTGGGACCACAGGCATGTACCACAGGCTAATTATT T C SMIM7,AC008764.4 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1055694215 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_349256 2243 RMVar_ID_2243 Human_SNP_ID_659952024 A-to-I Human chr19 - 16643111 16643109 16643111 AAATAACTTTTTTTTTCTTTTTTTAGAGACAGAGTCTCACTTGGCCAGGTGCGGTGGTTCACGCC AAATAACTTTTTTTTTCTTTTTTTAGAGACAG__TCTCACTTGGCCAGGTGCGGTGGTTCACGCC ACT A SMIM7,AC008764.4 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1036239227 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_241998,Human_RBP_ID_6725594,Human_RBP_ID_13389062,Human_RBP_ID_17568493 RMVar_hsa_circ_349256 2244 RMVar_ID_2244 Human_SNP_ID_659952146 A-to-I Human chr19 - 16643576 16643576 16643576 CCTGGCCAATATGGTGAAACCCTATCTCTACTAAACATACATATATTAGCTGGGCATAGTGGCAC CCTGGCCAATATGGTGAAACCCTATCTCTACTGAACATACATATATTAGCTGGGCATAGTGGCAC T C SMIM7,AC008764.4 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1183015548 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_349256 2245 RMVar_ID_2245 Human_SNP_ID_659952168 A-to-I Human chr19 - 16643639 16643639 16643639 TAATCCCAGCACTTTAGGAGGCTGAGGTGGGTAGATCACTTGAGGCCAGGAGTTCAATACCAGCC TAATCCCAGCACTTTAGGAGGCTGAGGTGGGTGGATCACTTGAGGCCAGGAGTTCAATACCAGCC T C SMIM7,AC008764.4 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1406057982 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_349256 2246 RMVar_ID_2246 Human_SNP_ID_659952188 A-to-I Human chr19 - 16643688 16643688 16643688 TACTTTGCTTGAAAAAATTTTTTAGGCCTGGTACGGTGGCTCATGCCTGTAATCCCAGCACTTTA TACTTTGCTTGAAAAAATTTTTTAGGCCTGGTGCGGTGGCTCATGCCTGTAATCCCAGCACTTTA T C SMIM7,AC008764.4 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1347457861 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_349256 2247 RMVar_ID_2247 Human_SNP_ID_659952401 A-to-I Human chr19 - 16644364 16644364 16644364 CAATCCCAGCATTTTGGGAGGCCAAAGTGGGCAGGTCACCTGTGGTCAGGAGTTCGAGACCAACC CAATCCCAGCATTTTGGGAGGCCAAAGTGGGCGGGTCACCTGTGGTCAGGAGTTCGAGACCAACC T C SMIM7,AC008764.4 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs990884419 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2558620 RMVar_hsa_circ_349256 2248 RMVar_ID_2248 Human_SNP_ID_659952489 A-to-I Human chr19 - 16644658 16644658 16644658 CCGAGGCAGGTGGATCACGAGGTCAGGAGTTCAAGAACAGCCTGGCCAAGATGGTGAAACCCCGT CCGAGGCAGGTGGATCACGAGGTCAGGAGTTCGAGAACAGCCTGGCCAAGATGGTGAAACCCCGT T C SMIM7,AC008764.4 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1209572629 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_349256 2249 RMVar_ID_2249 Human_SNP_ID_659952774 A-to-I Human chr19 - 16645770 16645770 16645770 ATAATCCCAGCTACTCGGGTGGCTGAGGCACAAGAATTGCTTAAATCTGGGAGGCGGAGGTTGCA ATAATCCCAGCTACTCGGGTGGCTGAGGCACAGGAATTGCTTAAATCTGGGAGGCGGAGGTTGCA T C SMIM7,AC008764.4 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs931192357 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_349256 2250 RMVar_ID_2250 Human_SNP_ID_659953221 A-to-I Human chr19 - 16647516 16647516 16647516 CGGATGCAGAGGTTGCAGCGAGCTGAGATCGCACCACTGTACTCCAGCCTGGGCGGCAGAGCCAG CGGATGCAGAGGTTGCAGCGAGCTGAGATCGCTCCACTGTACTCCAGCCTGGGCGGCAGAGCCAG T A SMIM7,AC008764.4 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1010260075 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25442539 RMVar_hsa_circ_193205,RMVar_hsa_circ_193204,RMVar_hsa_circ_287155,RMVar_hsa_circ_279806 2251 RMVar_ID_2251 Human_SNP_ID_659953222 A-to-I Human chr19 - 16647516 16647516 16647516 CGGATGCAGAGGTTGCAGCGAGCTGAGATCGCACCACTGTACTCCAGCCTGGGCGGCAGAGCCAG CGGATGCAGAGGTTGCAGCGAGCTGAGATCGCCCCACTGTACTCCAGCCTGGGCGGCAGAGCCAG T G SMIM7,AC008764.4 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1010260075 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25442539 RMVar_hsa_circ_193205,RMVar_hsa_circ_193204,RMVar_hsa_circ_287155,RMVar_hsa_circ_279806 2252 RMVar_ID_2252 Human_SNP_ID_659953743 A-to-I Human chr19 - 16649451 16649451 16649451 CTCCTGCCTCAGCCTCCTGAGTAACTGGGGTTACAGGTGTGCACCACCATGCCTAATTTTTTGTA CTCCTGCCTCAGCCTCCTGAGTAACTGGGGTTGCAGGTGTGCACCACCATGCCTAATTTTTTGTA T C SMIM7,AC008764.4 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs954392058 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193205,RMVar_hsa_circ_193204,RMVar_hsa_circ_287155,RMVar_hsa_circ_279806 2253 RMVar_ID_2253 Human_SNP_ID_659954042 A-to-I Human chr19 - 16650518 16650518 16650518 TTTGGTAGAGATGAGATTTCATCCTGTTGACCAGGCTGGTCTCGAACTCCTGACCTCAAATGATT TTTGGTAGAGATGAGATTTCATCCTGTTGACCGGGCTGGTCTCGAACTCCTGACCTCAAATGATT T C SMIM7,AC008764.4 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1418226120 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193205,RMVar_hsa_circ_193204,RMVar_hsa_circ_287155,RMVar_hsa_circ_279806 2254 RMVar_ID_2254 Human_SNP_ID_659954055 A-to-I Human chr19 - 16650561 16650561 16650561 AGACTACAGGCACGCACCACCACACTTGGCTAATTTTTCTATTTTTGGTAGAGATGAGATTTCAT AGACTACAGGCACGCACCACCACACTTGGCTAGTTTTTCTATTTTTGGTAGAGATGAGATTTCAT T C SMIM7,AC008764.4 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1423478823 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193205,RMVar_hsa_circ_193204,RMVar_hsa_circ_287155,RMVar_hsa_circ_279806 2255 RMVar_ID_2255 Human_SNP_ID_659954070 A-to-I Human chr19 - 16650602 16650602 16650602 AGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCAAGGAGCTGAGACTACAGGCACGCACCACCACA AGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCGAGGAGCTGAGACTACAGGCACGCACCACCACA T C SMIM7,AC008764.4 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs953487449 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193205,RMVar_hsa_circ_193204,RMVar_hsa_circ_287155,RMVar_hsa_circ_279806 2256 RMVar_ID_2256 Human_SNP_ID_659954984 A-to-I Human chr19 - 16653819 16653819 16653819 GCGATCTGGGCTCACTGCAACCTCGGCCTCTTAGGTCTAAGCGATTCTCCTGCCTCAGCCTCCCG GCGATCTGGGCTCACTGCAACCTCGGCCTCTTGGGTCTAAGCGATTCTCCTGCCTCAGCCTCCCG T C SMIM7,AC008764.4 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs757708527 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22230968 RMVar_hsa_circ_193205,RMVar_hsa_circ_193204,RMVar_hsa_circ_287155,RMVar_hsa_circ_279806,RMVar_hsa_circ_39530 2257 RMVar_ID_2257 Human_SNP_ID_659956765 A-to-I Human chr19 - 16660002 16660002 16660002 GGCGCCCCTAGTAACTGTAATTCTCCCTCTGCAGGACGTTGCTGATGAATGCCGGGGCGGTGCTG GGCGCCCCTAGTAACTGTAATTCTCCCTCTGCCGGACGTTGCTGATGAATGCCGGGGCGGTGCTG T G SMIM7,AC008764.4 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) 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 2258 RMVar_ID_2258 Human_SNP_ID_659958626 A-to-I Human chr19 + 16666697 16666697 16666697 GAAATGCAGAGCCCCTGCGGTGGCTCATGCCTATAGTCCCAGCACTTTGGGAAGCCAAGGTGGCT GAAATGCAGAGCCCCTGCGGTGGCTCATGCCTGTAGTCCCAGCACTTTGGGAAGCCAAGGTGGCT A G TMEM38A Ensembl:ENSG00000072954 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1214837262 Functional Loss SNV dbSNP153 33..33 33 - - - 2259 RMVar_ID_2259 Human_SNP_ID_659963073 A-to-I Human chr19 + 16682997 16682996 16682998 TTAATGTTTTTTATTTTTTTATTTTTTGAGACAGAGTCTTGCTCTGTCGCCCAGGCTTGAGTATG TTAATGTTTTTTATTTTTTTATTTTTTGAGAC__AGTCTTGCTCTGTCGCCCAGGCTTGAGTATG CAG C TMEM38A Ensembl:ENSG00000072954 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs975558705 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_2558643 RMVar_hsa_circ_344973 2260 RMVar_ID_2260 Human_SNP_ID_659963094 A-to-I Human chr19 + 16683115 16683115 16683115 CGTGCCTCAGCCTCCTGAGTACCTGGGATTACAGGCATGTGCCACCATGCCCGGCTAATTTTTGT CGTGCCTCAGCCTCCTGAGTACCTGGGATTACCGGCATGTGCCACCATGCCCGGCTAATTTTTGT A C TMEM38A Ensembl:ENSG00000072954 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1473978973 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_344973 2261 RMVar_ID_2261 Human_SNP_ID_659963132 A-to-I Human chr19 + 16683248 16683248 16683248 TGCCGACCTCAGCCTCCCAAAATACCGGGATTACAGGCATGAGCCACCCTGCCCTGGACAGTTTA TGCCGACCTCAGCCTCCCAAAATACCGGGATTGCAGGCATGAGCCACCCTGCCCTGGACAGTTTA A G TMEM38A Ensembl:ENSG00000072954 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs138578846 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_344973 2262 RMVar_ID_2262 Human_SNP_ID_660004590 A-to-I Human chr19 + 16833986 16833986 16833986 TGACCCCGTGATTCGCCCACCTCTGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCAC TGACCCCGTGATTCGCCCACCTCTGCCTCCCAGAGTGCTGGGATTACAGGTGTGAGCCACCGCAC A G SIN3B Ensembl:ENSG00000127511 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1306686626 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77626,RMVar_hsa_circ_346912,RMVar_hsa_circ_23373,RMVar_hsa_circ_26759,RMVar_hsa_circ_193214 2263 RMVar_ID_2263 Human_SNP_ID_660006010 A-to-I Human chr19 + 16839220 16839220 16839220 AAACTCCTGACTTCAAGGGATCTGTCCACCTCAACCTCCCAAAGTGCTAGAATTACAGGTGTGAG AAACTCCTGACTTCAAGGGATCTGTCCACCTCGACCTCCCAAAGTGCTAGAATTACAGGTGTGAG A G SIN3B Ensembl:ENSG00000127511 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202478500 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77626,RMVar_hsa_circ_346912,RMVar_hsa_circ_23373,RMVar_hsa_circ_26759,RMVar_hsa_circ_193214 2264 RMVar_ID_2264 Human_SNP_ID_660010442 A-to-I Human chr19 + 16855482 16855482 16855482 CGGTGGCTCGTGTGTAATCCCAGCACTTTGGGAGGCCGAGGTGAGCAGATTGCCTGAGGTCAGGA CGGTGGCTCGTGTGTAATCCCAGCACTTTGGGCGGCCGAGGTGAGCAGATTGCCTGAGGTCAGGA A C SIN3B Ensembl:ENSG00000127511 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1279660006 Functional Loss SNV dbSNP153 33..33 33 - - - 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 2265 RMVar_ID_2265 Human_SNP_ID_660010451 A-to-I Human chr19 + 16855506 16855506 16855506 ACTTTGGGAGGCCGAGGTGAGCAGATTGCCTGAGGTCAGGAGTTGGAGACAAGCCTGGCCAACAT ACTTTGGGAGGCCGAGGTGAGCAGATTGCCTGTGGTCAGGAGTTGGAGACAAGCCTGGCCAACAT A T SIN3B Ensembl:ENSG00000127511 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1363664434 Functional Loss SNV dbSNP153 33..33 33 - - - 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 2266 RMVar_ID_2266 Human_SNP_ID_660010460 A-to-I Human chr19 + 16855534 16855534 16855534 CCTGAGGTCAGGAGTTGGAGACAAGCCTGGCCAACATGGTGGAACTCCATCTCTACTAAAAATAC CCTGAGGTCAGGAGTTGGAGACAAGCCTGGCCGACATGGTGGAACTCCATCTCTACTAAAAATAC A G SIN3B Ensembl:ENSG00000127511 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1479515856 Functional Loss SNV dbSNP153 33..33 33 - - - 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 2267 RMVar_ID_2267 Human_SNP_ID_660010470 A-to-I Human chr19 + 16855556 16855556 16855556 AAGCCTGGCCAACATGGTGGAACTCCATCTCTACTAAAAATACAAAAATTAGCCGGGCGTGGTGG AAGCCTGGCCAACATGGTGGAACTCCATCTCTGCTAAAAATACAAAAATTAGCCGGGCGTGGTGG A G SIN3B Ensembl:ENSG00000127511 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1477656788 Functional Loss SNV dbSNP153 33..33 33 - - - 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 2268 RMVar_ID_2268 Human_SNP_ID_660010471 A-to-I Human chr19 + 16855559 16855559 16855559 CCTGGCCAACATGGTGGAACTCCATCTCTACTAAAAATACAAAAATTAGCCGGGCGTGGTGGCAG CCTGGCCAACATGGTGGAACTCCATCTCTACTGAAAATACAAAAATTAGCCGGGCGTGGTGGCAG A G SIN3B Ensembl:ENSG00000127511 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1361407576 Functional Loss SNV dbSNP153 33..33 33 - - - 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 2269 RMVar_ID_2269 Human_SNP_ID_660010472 A-to-I Human chr19 + 16855570 16855570 16855570 TGGTGGAACTCCATCTCTACTAAAAATACAAAAATTAGCCGGGCGTGGTGGCAGGCGCCTGTAAT TGGTGGAACTCCATCTCTACTAAAAATACAAATATTAGCCGGGCGTGGTGGCAGGCGCCTGTAAT A T SIN3B Ensembl:ENSG00000127511 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1000764998 Functional Loss SNV dbSNP153 33..33 33 - - - 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 2270 RMVar_ID_2270 Human_SNP_ID_660010494 A-to-I Human chr19 + 16855646 16855646 16855646 GGGAGGCTGAGGCAGGAGAATCGCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCTGAGATCACG GGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGGGAGGCGGAGGTTGCAGTGAGCTGAGATCACG A G SIN3B Ensembl:ENSG00000127511 Protein coding intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1232681825 Functional Loss SNV dbSNP153 33..33 33 - - - 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 2271 RMVar_ID_2271 Human_SNP_ID_660010500 A-to-I Human chr19 + 16855666 16855664 16855666 TCGCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCTGAGATCACGCCATTGTACTCCAGCCTGGG TCGCTTGAACCCAGGAGGCGGAGGTTGCAGT__GCTGAGATCACGCCATTGTACTCCAGCCTGGG TGA T SIN3B Ensembl:ENSG00000127511 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1326117466 Functional Loss DEL dbSNP153 32..33 33 - - - 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 2272 RMVar_ID_2272 Human_SNP_ID_660010502 A-to-I Human chr19 + 16855676 16855676 16855676 CCAGGAGGCGGAGGTTGCAGTGAGCTGAGATCACGCCATTGTACTCCAGCCTGGGTGGCGACAAG CCAGGAGGCGGAGGTTGCAGTGAGCTGAGATCGCGCCATTGTACTCCAGCCTGGGTGGCGACAAG A G SIN3B Ensembl:ENSG00000127511 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229 RNA-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 2273 RMVar_ID_2273 Human_SNP_ID_660013038 A-to-I Human chr19 + 16865171 16865171 16865171 TTTTAATTAGCCAGGCATGGTGGTGCACACCTATATTCCTAGCTACGTGGGAGGCTAAGGTGGGA TTTTAATTAGCCAGGCATGGTGGTGCACACCTGTATTCCTAGCTACGTGGGAGGCTAAGGTGGGA A G SIN3B Ensembl:ENSG00000127511 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1254674814 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77626,RMVar_hsa_circ_373268,RMVar_hsa_circ_193214,RMVar_hsa_circ_193218,RMVar_hsa_circ_193222,RMVar_hsa_circ_269527,RMVar_hsa_circ_302830,RMVar_hsa_circ_307803,RMVar_hsa_circ_360531,RMVar_hsa_circ_193223 2274 RMVar_ID_2274 Human_SNP_ID_660065644 A-to-I Human chr19 - 17051714 17051714 17051714 GTAATGAGCTGTGGTCGTGCCACTGCATTACAACCTGAGCAGTAGAGTGAGACCCTGTCTCAGGA GTAATGAGCTGTGGTCGTGCCACTGCATTACAGCCTGAGCAGTAGAGTGAGACCCTGTCTCAGGA T C HAUS8 Ensembl:ENSG00000131351 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1056214239 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193226,RMVar_hsa_circ_119212 2275 RMVar_ID_2275 Human_SNP_ID_660065738 A-to-I Human chr19 - 17052101 17052101 17052101 TTTTGAGACAGAGTTGCTCAGGCTTAAGTGCAATGTCATGATTTTGGCTCACTGCAACCTCCACC TTTTGAGACAGAGTTGCTCAGGCTTAAGTGCAGTGTCATGATTTTGGCTCACTGCAACCTCCACC T C HAUS8 Ensembl:ENSG00000131351 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1568633253 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193226,RMVar_hsa_circ_119212 2276 RMVar_ID_2276 Human_SNP_ID_660066518 A-to-I Human chr19 - 17054762 17054762 17054762 AGTTTCACTCTTGTTGCCCAGGCTGGAGTGCAATGGTGCAATCCTGGCTCTCTGCAACCTCCACC AGTTTCACTCTTGTTGCCCAGGCTGGAGTGCAGTGGTGCAATCCTGGCTCTCTGCAACCTCCACC T C HAUS8 Ensembl:ENSG00000131351 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1568634585 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7491,RMVar_hsa_circ_193226,RMVar_hsa_circ_119212,RMVar_hsa_circ_375462,RMVar_hsa_circ_193227 2277 RMVar_ID_2277 Human_SNP_ID_660067297 A-to-I Human chr19 - 17056746 17056746 17056746 TCTCTACTAAAAATACAAAAAATTAGCTGGGCATGGTGATGCGTGCCTGTAACCCAGCTACTTGG TCTCTACTAAAAATACAAAAAATTAGCTGGGCGTGGTGATGCGTGCCTGTAACCCAGCTACTTGG T C HAUS8 Ensembl:ENSG00000131351 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs896489653 Functional Loss SNV dbSNP153 33..33 33 - - - 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_193228 2278 RMVar_ID_2278 Human_SNP_ID_660067334 A-to-I Human chr19 - 17056913 17056913 17056913 ATCACTCCACAGCACTCCACCTTGGGCAACACAGTAAGATCTGTCTATAAAAAATATGTATGTGC ATCACTCCACAGCACTCCACCTTGGGCAACACGGTAAGATCTGTCTATAAAAAATATGTATGTGC T C HAUS8 Ensembl:ENSG00000131351 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs73504817 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_18,GWAS_ID_19,GWAS_ID_20,GWAS_ID_21,GWAS_ID_22,GWAS_ID_23,GWAS_ID_24,GWAS_ID_25,GWAS_ID_26 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_193228 2279 RMVar_ID_2279 Human_SNP_ID_660067335 A-to-I Human chr19 - 17056913 17056913 17056913 ATCACTCCACAGCACTCCACCTTGGGCAACACAGTAAGATCTGTCTATAAAAAATATGTATGTGC ATCACTCCACAGCACTCCACCTTGGGCAACACCGTAAGATCTGTCTATAAAAAATATGTATGTGC T G HAUS8 Ensembl:ENSG00000131351 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs73504817 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_18,GWAS_ID_19,GWAS_ID_20,GWAS_ID_21,GWAS_ID_22,GWAS_ID_23,GWAS_ID_24,GWAS_ID_25,GWAS_ID_26 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_193228 2280 RMVar_ID_2280 Human_SNP_ID_660067412 A-to-I Human chr19 - 17057274 17057274 17057274 GCTGTCTCAGCTCACTGCAACGTCCGCCTCCCAGGTTCAGGCAACTCTCATACCTGAGCTTCCTG GCTGTCTCAGCTCACTGCAACGTCCGCCTCCCTGGTTCAGGCAACTCTCATACCTGAGCTTCCTG T A HAUS8 Ensembl:ENSG00000131351 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1370791842 Functional Loss SNV dbSNP153 33..33 33 - - - 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_193228 2281 RMVar_ID_2281 Human_SNP_ID_660067418 A-to-I Human chr19 - 17057293 17057293 17057293 CAGGCTGTAGTGCAGTGGTGCTGTCTCAGCTCACTGCAACGTCCGCCTCCCAGGTTCAGGCAACT CAGGCTGTAGTGCAGTGGTGCTGTCTCAGCTCTCTGCAACGTCCGCCTCCCAGGTTCAGGCAACT T A HAUS8 Ensembl:ENSG00000131351 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs937834192 Functional Loss SNV dbSNP153 33..33 33 - - - 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_193228 2282 RMVar_ID_2282 Human_SNP_ID_660070385 A-to-I Human chr19 - 17068672 17068672 17068672 GCCTCAGCCTCCCAGGCTCAAGCCATCTTCCCACCTGAGCCTTCTGAGTAACTGGGACGAAAGGC GCCTCAGCCTCCCAGGCTCAAGCCATCTTCCCGCCTGAGCCTTCTGAGTAACTGGGACGAAAGGC T C HAUS8 Ensembl:ENSG00000131351 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1323380771 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2342,RMVar_hsa_circ_193226,RMVar_hsa_circ_119212,RMVar_hsa_circ_322666 2283 RMVar_ID_2283 Human_SNP_ID_660071073 A-to-I Human chr19 - 17070948 17070948 17070948 CTCCTGCCTCAGTCTCCCAAGTAGCTGGGATTACAGGCACATGCCACCACGCCTGGCTAATTTCT CTCCTGCCTCAGTCTCCCAAGTAGCTGGGATTGCAGGCACATGCCACCACGCCTGGCTAATTTCT T C HAUS8 Ensembl:ENSG00000131351 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1175625498 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193226,RMVar_hsa_circ_119212,RMVar_hsa_circ_322666,RMVar_hsa_circ_92389,RMVar_hsa_circ_193231 2284 RMVar_ID_2284 Human_SNP_ID_660071074 A-to-I Human chr19 - 17070961 17070961 17070961 GATTCCAGTGATTCTCCTGCCTCAGTCTCCCAAGTAGCTGGGATTACAGGCACATGCCACCACGC GATTCCAGTGATTCTCCTGCCTCAGTCTCCCAGGTAGCTGGGATTACAGGCACATGCCACCACGC T C HAUS8 Ensembl:ENSG00000131351 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs906198822 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193226,RMVar_hsa_circ_119212,RMVar_hsa_circ_322666,RMVar_hsa_circ_92389,RMVar_hsa_circ_193231 2285 RMVar_ID_2285 Human_SNP_ID_660074634 A-to-I Human chr19 + 17083776 17083769 17083776 TCAAGTTACCGATTCTCCTGCCTCAGCCTCCCAAGTAGGTGGGGTTACAGGCACCCGCTACCACG TCAAGTTACCGATTCTCCTGCCTCAG_______AGTAGGTGGGGTTACAGGCACCCGCTACCACG GCCTCCCA G MYO9B Ensembl:ENSG00000099331 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1431127746 Functional Loss DEL dbSNP153 27..33 33 - - - RMVar_hsa_circ_122375,RMVar_hsa_circ_193233,RMVar_hsa_circ_86637,RMVar_hsa_circ_193232 2286 RMVar_ID_2286 Human_SNP_ID_660078848 A-to-I Human chr19 + 17098747 17098747 17098747 GCCCAGGAGTTTGACAACAACCTGGGCAATATAGTGAGGCCCCCATCTCTACAGAAAATACAGAA GCCCAGGAGTTTGACAACAACCTGGGCAATATGGTGAGGCCCCCATCTCTACAGAAAATACAGAA A G MYO9B Ensembl:ENSG00000099331 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1430142397 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122375,RMVar_hsa_circ_193233,RMVar_hsa_circ_86637,RMVar_hsa_circ_193232 2287 RMVar_ID_2287 Human_SNP_ID_660080096 A-to-I Human chr19 + 17102651 17102651 17102651 GGCCAAGCTCGGTGGCCCACATCTATAATCCCAATGCTTTGGAAGGCTGAGGGAGGAGGATTGCT GGCCAAGCTCGGTGGCCCACATCTATAATCCCGATGCTTTGGAAGGCTGAGGGAGGAGGATTGCT A G MYO9B Ensembl:ENSG00000099331 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs972408498 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39561,RMVar_hsa_circ_193233,RMVar_hsa_circ_86637,RMVar_hsa_circ_23647,RMVar_hsa_circ_26650,RMVar_hsa_circ_6029 2288 RMVar_ID_2288 Human_SNP_ID_660080615 A-to-I Human chr19 + 17104628 17104628 17104628 TTTATTTTTTGTAGAGATGGGGGTCTCACTGTATTCCCCAGGCTGGTCTCGAACTCCTGGATGCC TTTATTTTTTGTAGAGATGGGGGTCTCACTGTGTTCCCCAGGCTGGTCTCGAACTCCTGGATGCC A G MYO9B Ensembl:ENSG00000099331 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1445765874 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39561,RMVar_hsa_circ_193233,RMVar_hsa_circ_86637,RMVar_hsa_circ_23647,RMVar_hsa_circ_26650,RMVar_hsa_circ_6029 2289 RMVar_ID_2289 Human_SNP_ID_660080821 A-to-I Human chr19 + 17105384 17105384 17105384 AGGTGTGGTGGTGTTTGCCTGTGGTCCCCCCTACGTGGGAGTCTGAGGCAGGAGAATCGCTTGAG AGGTGTGGTGGTGTTTGCCTGTGGTCCCCCCTGCGTGGGAGTCTGAGGCAGGAGAATCGCTTGAG A G MYO9B Ensembl:ENSG00000099331 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs140956196 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39561,RMVar_hsa_circ_193233,RMVar_hsa_circ_86637,RMVar_hsa_circ_23647,RMVar_hsa_circ_26650,RMVar_hsa_circ_6029 2290 RMVar_ID_2290 Human_SNP_ID_660080993 A-to-I Human chr19 + 17106082 17106082 17106082 TGGAGTGCAGTGGCACAATCATAACTCACCGCAGCCTCGAGAACTTCTGGGCTCAAGCGATCCTC TGGAGTGCAGTGGCACAATCATAACTCACCGCTGCCTCGAGAACTTCTGGGCTCAAGCGATCCTC A T MYO9B Ensembl:ENSG00000099331 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1367216806 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39561,RMVar_hsa_circ_193233,RMVar_hsa_circ_86637,RMVar_hsa_circ_23647,RMVar_hsa_circ_26650,RMVar_hsa_circ_6029 2291 RMVar_ID_2291 Human_SNP_ID_660084744 A-to-I Human chr19 + 17120057 17120057 17120057 GTGCTGGCGCATGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGTGGGAGGATTGCAGGCCCATG GTGCTGGCGCATGCCTGTAGTCCCAGCTACTCCGGAGGCTGAGGTGGGAGGATTGCAGGCCCATG A C MYO9B Ensembl:ENSG00000099331 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs770514965 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39561,RMVar_hsa_circ_193233,RMVar_hsa_circ_86637,RMVar_hsa_circ_23647,RMVar_hsa_circ_26650,RMVar_hsa_circ_6029 2292 RMVar_ID_2292 Human_SNP_ID_660084745 A-to-I Human chr19 + 17120057 17120057 17120057 GTGCTGGCGCATGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGTGGGAGGATTGCAGGCCCATG GTGCTGGCGCATGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGTGGGAGGATTGCAGGCCCATG A G MYO9B Ensembl:ENSG00000099331 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs770514965 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39561,RMVar_hsa_circ_193233,RMVar_hsa_circ_86637,RMVar_hsa_circ_23647,RMVar_hsa_circ_26650,RMVar_hsa_circ_6029 2293 RMVar_ID_2293 Human_SNP_ID_660090148 A-to-I Human chr19 + 17139520 17139520 17139520 TAATCTCAACACTTTGAGAGGCCAAAGTATGCAGATTGCTTGAGCCCAGGAGTTTGAGACTGGCC TAATCTCAACACTTTGAGAGGCCAAAGTATGCGGATTGCTTGAGCCCAGGAGTTTGAGACTGGCC A G MYO9B Ensembl:ENSG00000099331 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs751810697 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39561,RMVar_hsa_circ_193233,RMVar_hsa_circ_86637,RMVar_hsa_circ_23647,RMVar_hsa_circ_26650,RMVar_hsa_circ_6029 2294 RMVar_ID_2294 Human_SNP_ID_660093572 A-to-I Human chr19 + 17152366 17152366 17152366 CTTGACATAGGTCAAGAGTTTGAGATCAGCCTAGCCAACATGGCAAAACCCCGCCTCTACTAAAA CTTGACATAGGTCAAGAGTTTGAGATCAGCCTGGCCAACATGGCAAAACCCCGCCTCTACTAAAA A G MYO9B Ensembl:ENSG00000099331 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1007473355 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18052,RMVar_hsa_circ_193233,RMVar_hsa_circ_86637,RMVar_hsa_circ_23647,RMVar_hsa_circ_26650,RMVar_hsa_circ_6029,RMVar_hsa_circ_322949,RMVar_hsa_circ_347442,RMVar_hsa_circ_375717,RMVar_hsa_circ_335668,RMVar_hsa_circ_99075,RMVar_hsa_circ_193236,RMVar_hsa_circ_193238,RMVar_hsa_circ_193239,RMVar_hsa_circ_193240,RMVar_hsa_circ_193237 2295 RMVar_ID_2295 Human_SNP_ID_660094340 A-to-I Human chr19 + 17154851 17154850 17154851 AGGCGTGGTAGTATGCACCTGTGGTCCCAGCTACTTGTGGGGCTGAGGTGGGAGGATCACTTGGG AGGCGTGGTAGTATGCACCTGTGGTCCCAGCT_CTTGTGGGGCTGAGGTGGGAGGATCACTTGGG TA T MYO9B Ensembl:ENSG00000099331 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1417096052 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_28502,RMVar_hsa_circ_18052,RMVar_hsa_circ_193233,RMVar_hsa_circ_86637,RMVar_hsa_circ_23647,RMVar_hsa_circ_26650,RMVar_hsa_circ_6029,RMVar_hsa_circ_322949,RMVar_hsa_circ_347442,RMVar_hsa_circ_375717,RMVar_hsa_circ_99075,RMVar_hsa_circ_193238,RMVar_hsa_circ_193239,RMVar_hsa_circ_193240,RMVar_hsa_circ_193237,RMVar_hsa_circ_193241,RMVar_hsa_circ_275686,RMVar_hsa_circ_342472,RMVar_hsa_circ_370365,RMVar_hsa_circ_285977,RMVar_hsa_circ_193243,RMVar_hsa_circ_193242,RMVar_hsa_circ_193246,RMVar_hsa_circ_29548,RMVar_hsa_circ_304394,RMVar_hsa_circ_315708,RMVar_hsa_circ_298793,RMVar_hsa_circ_193247,RMVar_hsa_circ_193245 2296 RMVar_ID_2296 Human_SNP_ID_660094444 A-to-I Human chr19 + 17155328 17155328 17155328 CTCCCACCTCAGCCTCCCAAGCAGCTGGGACTACAGGCGCGTGCCACCACACCTGGACAATTTTT CTCCCACCTCAGCCTCCCAAGCAGCTGGGACTGCAGGCGCGTGCCACCACACCTGGACAATTTTT A G MYO9B Ensembl:ENSG00000099331 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1344186250 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28502,RMVar_hsa_circ_18052,RMVar_hsa_circ_193233,RMVar_hsa_circ_86637,RMVar_hsa_circ_23647,RMVar_hsa_circ_26650,RMVar_hsa_circ_6029,RMVar_hsa_circ_322949,RMVar_hsa_circ_347442,RMVar_hsa_circ_375717,RMVar_hsa_circ_99075,RMVar_hsa_circ_193238,RMVar_hsa_circ_193239,RMVar_hsa_circ_193240,RMVar_hsa_circ_193237,RMVar_hsa_circ_193241,RMVar_hsa_circ_275686,RMVar_hsa_circ_342472,RMVar_hsa_circ_370365,RMVar_hsa_circ_285977,RMVar_hsa_circ_193243,RMVar_hsa_circ_193242,RMVar_hsa_circ_193246,RMVar_hsa_circ_29548,RMVar_hsa_circ_304394,RMVar_hsa_circ_315708,RMVar_hsa_circ_298793,RMVar_hsa_circ_193247,RMVar_hsa_circ_193245 2297 RMVar_ID_2297 Human_SNP_ID_660095753 A-to-I Human chr19 + 17160647 17160647 17160647 TTCATGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGTGTGCGCCACTAGGCCTGGCTAATTTTT TTCATGCCTCAGCCTCCTGAGTAGCTGGGATTGCAGGTGTGCGCCACTAGGCCTGGCTAATTTTT A G MYO9B Ensembl:ENSG00000099331 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs147068408 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28502,RMVar_hsa_circ_18052,RMVar_hsa_circ_23647,RMVar_hsa_circ_347442,RMVar_hsa_circ_375717,RMVar_hsa_circ_193239,RMVar_hsa_circ_193240,RMVar_hsa_circ_193241,RMVar_hsa_circ_275686,RMVar_hsa_circ_370365,RMVar_hsa_circ_29548,RMVar_hsa_circ_298793,RMVar_hsa_circ_193247,RMVar_hsa_circ_193249,RMVar_hsa_circ_72542,RMVar_hsa_circ_290951,RMVar_hsa_circ_297369,RMVar_hsa_circ_289445,RMVar_hsa_circ_83449,RMVar_hsa_circ_193250,RMVar_hsa_circ_193253,RMVar_hsa_circ_310577,RMVar_hsa_circ_346486,RMVar_hsa_circ_193248,RMVar_hsa_circ_335768,RMVar_hsa_circ_294764,RMVar_hsa_circ_193252 2298 RMVar_ID_2298 Human_SNP_ID_660098070 A-to-I Human chr19 + 17169476 17169476 17169476 CCCCATCTCTACTAAAAATGCAAAAATTAGCCAGGCATGGTGGCGGGTGCCTATAATTCCAGCTA CCCCATCTCTACTAAAAATGCAAAAATTAGCCGGGCATGGTGGCGGGTGCCTATAATTCCAGCTA A G MYO9B Ensembl:ENSG00000099331 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1418749664 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28502,RMVar_hsa_circ_18052,RMVar_hsa_circ_29548,RMVar_hsa_circ_72542,RMVar_hsa_circ_297369,RMVar_hsa_circ_346486,RMVar_hsa_circ_335768,RMVar_hsa_circ_298820,RMVar_hsa_circ_328984,RMVar_hsa_circ_343922,RMVar_hsa_circ_20038,RMVar_hsa_circ_335234 2299 RMVar_ID_2299 Human_SNP_ID_660098231 A-to-I Human chr19 + 17170004 17170004 17170004 GCTGGGATCACAGGTGCCTTGCCACCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGT GCTGGGATCACAGGTGCCTTGCCACCATGCCCGGCTAATTTTTGTATTTTTAGTAGAGATGGGGT A G MYO9B Ensembl:ENSG00000099331 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1191193217 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28502,RMVar_hsa_circ_18052,RMVar_hsa_circ_29548,RMVar_hsa_circ_72542,RMVar_hsa_circ_297369,RMVar_hsa_circ_346486,RMVar_hsa_circ_335768,RMVar_hsa_circ_298820,RMVar_hsa_circ_328984,RMVar_hsa_circ_343922,RMVar_hsa_circ_20038,RMVar_hsa_circ_335234 2300 RMVar_ID_2300 Human_SNP_ID_660098232 A-to-I Human chr19 + 17170008 17170007 17170008 GGATCACAGGTGCCTTGCCACCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTTT GGATCACAGGTGCCTTGCCACCATGCCCAGCT_ATTTTTGTATTTTTAGTAGAGATGGGGTTTTT TA T MYO9B Ensembl:ENSG00000099331 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1418368362 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_28502,RMVar_hsa_circ_18052,RMVar_hsa_circ_29548,RMVar_hsa_circ_72542,RMVar_hsa_circ_297369,RMVar_hsa_circ_346486,RMVar_hsa_circ_335768,RMVar_hsa_circ_298820,RMVar_hsa_circ_328984,RMVar_hsa_circ_343922,RMVar_hsa_circ_20038,RMVar_hsa_circ_335234 2301 RMVar_ID_2301 Human_SNP_ID_660098455 A-to-I Human chr19 + 17170763 17170763 17170763 GGAGGATCACTTGAGCCCAGAGAGTCAAGGCTACAGTGAGTTGTGATTGTACCATTGCATTCTAG GGAGGATCACTTGAGCCCAGAGAGTCAAGGCTTCAGTGAGTTGTGATTGTACCATTGCATTCTAG A T MYO9B Ensembl:ENSG00000099331 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs922247381 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28502,RMVar_hsa_circ_18052,RMVar_hsa_circ_29548,RMVar_hsa_circ_72542,RMVar_hsa_circ_297369,RMVar_hsa_circ_346486,RMVar_hsa_circ_335768,RMVar_hsa_circ_298820,RMVar_hsa_circ_328984,RMVar_hsa_circ_343922,RMVar_hsa_circ_20038,RMVar_hsa_circ_335234 2302 RMVar_ID_2302 Human_SNP_ID_660099174 A-to-I Human chr19 + 17173430 17173430 17173430 GGGTTCAAGCGATTCTCCTGCTTCACCCTCCCAAGTAGCTGGGACTACAGGTTACCGCCACCACA GGGTTCAAGCGATTCTCCTGCTTCACCCTCCCGAGTAGCTGGGACTACAGGTTACCGCCACCACA A G MYO9B Ensembl:ENSG00000099331 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1201179029 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28502,RMVar_hsa_circ_18052,RMVar_hsa_circ_29548,RMVar_hsa_circ_297369,RMVar_hsa_circ_346486,RMVar_hsa_circ_298820,RMVar_hsa_circ_343922,RMVar_hsa_circ_335234,RMVar_hsa_circ_364533 2303 RMVar_ID_2303 Human_SNP_ID_660099390 A-to-I Human chr19 + 17174213 17174213 17174213 CACCACGCCTGGCTAATTGTTTTGTATTTTTTAGTAGAGATAGGGTTTCACCATGTTAGCCAGGA CACCACGCCTGGCTAATTGTTTTGTATTTTTTCGTAGAGATAGGGTTTCACCATGTTAGCCAGGA A C MYO9B Ensembl:ENSG00000099331 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs746112860 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28502,RMVar_hsa_circ_18052,RMVar_hsa_circ_29548,RMVar_hsa_circ_297369,RMVar_hsa_circ_346486,RMVar_hsa_circ_298820,RMVar_hsa_circ_343922,RMVar_hsa_circ_335234,RMVar_hsa_circ_364533 2304 RMVar_ID_2304 Human_SNP_ID_660099393 A-to-I Human chr19 + 17174222 17174222 17174222 TGGCTAATTGTTTTGTATTTTTTAGTAGAGATAGGGTTTCACCATGTTAGCCAGGATGGTCTCGA TGGCTAATTGTTTTGTATTTTTTAGTAGAGATGGGGTTTCACCATGTTAGCCAGGATGGTCTCGA A G MYO9B Ensembl:ENSG00000099331 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1021579005 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28502,RMVar_hsa_circ_18052,RMVar_hsa_circ_29548,RMVar_hsa_circ_297369,RMVar_hsa_circ_346486,RMVar_hsa_circ_298820,RMVar_hsa_circ_343922,RMVar_hsa_circ_335234,RMVar_hsa_circ_364533 2305 RMVar_ID_2305 Human_SNP_ID_660099477 A-to-I Human chr19 + 17174501 17174501 17174501 TACTAAAAATGCAAATATTAGCCAGGCATGGTAGTGCATGCCTGTGGTCCCAGCTACCACAGGGA TACTAAAAATGCAAATATTAGCCAGGCATGGTCGTGCATGCCTGTGGTCCCAGCTACCACAGGGA A C MYO9B Ensembl:ENSG00000099331 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs112861150 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_27,GWAS_ID_28,GWAS_ID_29,GWAS_ID_30,GWAS_ID_31,GWAS_ID_32,GWAS_ID_33,GWAS_ID_34,GWAS_ID_35,GWAS_ID_36,GWAS_ID_37,GWAS_ID_38,GWAS_ID_39,GWAS_ID_40,GWAS_ID_41,GWAS_ID_42,GWAS_ID_43,GWAS_ID_44 RMVar_hsa_circ_28502,RMVar_hsa_circ_18052,RMVar_hsa_circ_29548,RMVar_hsa_circ_297369,RMVar_hsa_circ_346486,RMVar_hsa_circ_298820,RMVar_hsa_circ_343922,RMVar_hsa_circ_335234,RMVar_hsa_circ_364533 2306 RMVar_ID_2306 Human_SNP_ID_660099478 A-to-I Human chr19 + 17174501 17174501 17174501 TACTAAAAATGCAAATATTAGCCAGGCATGGTAGTGCATGCCTGTGGTCCCAGCTACCACAGGGA TACTAAAAATGCAAATATTAGCCAGGCATGGTGGTGCATGCCTGTGGTCCCAGCTACCACAGGGA A G MYO9B Ensembl:ENSG00000099331 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs112861150 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_27,GWAS_ID_28,GWAS_ID_29,GWAS_ID_30,GWAS_ID_31,GWAS_ID_32,GWAS_ID_33,GWAS_ID_34,GWAS_ID_35,GWAS_ID_36,GWAS_ID_37,GWAS_ID_38,GWAS_ID_39,GWAS_ID_40,GWAS_ID_41,GWAS_ID_42,GWAS_ID_43,GWAS_ID_44 RMVar_hsa_circ_28502,RMVar_hsa_circ_18052,RMVar_hsa_circ_29548,RMVar_hsa_circ_297369,RMVar_hsa_circ_346486,RMVar_hsa_circ_298820,RMVar_hsa_circ_343922,RMVar_hsa_circ_335234,RMVar_hsa_circ_364533 2307 RMVar_ID_2307 Human_SNP_ID_660099584 A-to-I Human chr19 + 17174849 17174849 17174849 CCAGCTACTCAGGAGGCCGAGGCAGGAGAATCACTTAAACCGGGGAGGCAGAGGTTGCAGTGAGC CCAGCTACTCAGGAGGCCGAGGCAGGAGAATCGCTTAAACCGGGGAGGCAGAGGTTGCAGTGAGC A G MYO9B Ensembl:ENSG00000099331 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1392045680 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28502,RMVar_hsa_circ_18052,RMVar_hsa_circ_29548,RMVar_hsa_circ_297369,RMVar_hsa_circ_346486,RMVar_hsa_circ_298820,RMVar_hsa_circ_343922,RMVar_hsa_circ_335234,RMVar_hsa_circ_364533 2308 RMVar_ID_2308 Human_SNP_ID_660099787 A-to-I Human chr19 + 17175360 17175360 17175360 TAATCCCAGGATTTTGGGAGGCCAAGGTGGGCAGATCACCTGAGGTCAGGAGTTCAAGACCAGCC TAATCCCAGGATTTTGGGAGGCCAAGGTGGGCGGATCACCTGAGGTCAGGAGTTCAAGACCAGCC A G MYO9B Ensembl:ENSG00000099331 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs933902336 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28502,RMVar_hsa_circ_18052,RMVar_hsa_circ_29548,RMVar_hsa_circ_297369,RMVar_hsa_circ_346486,RMVar_hsa_circ_298820,RMVar_hsa_circ_343922,RMVar_hsa_circ_335234,RMVar_hsa_circ_364533 2309 RMVar_ID_2309 Human_SNP_ID_660100156 A-to-I Human chr19 + 17176423 17176423 17176423 GAACTCCTGACCTTGGGTGATCCACCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG GAACTCCTGACCTTGGGTGATCCACCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG A G MYO9B Ensembl:ENSG00000099331 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs575868536 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28502,RMVar_hsa_circ_6728,RMVar_hsa_circ_113476,RMVar_hsa_circ_316775,RMVar_hsa_circ_60080,RMVar_hsa_circ_193258,RMVar_hsa_circ_193259 2310 RMVar_ID_2310 Human_SNP_ID_660100295 A-to-I Human chr19 + 17177014 17177014 17177014 CTTGAGGTCGGGCGTTTGAGACCCGCCTGGCCAACATGGTGAAACCTCGTCTCTACTAAAAATAC CTTGAGGTCGGGCGTTTGAGACCCGCCTGGCCGACATGGTGAAACCTCGTCTCTACTAAAAATAC A G MYO9B Ensembl:ENSG00000099331 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1222704372 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28502,RMVar_hsa_circ_6728,RMVar_hsa_circ_113476,RMVar_hsa_circ_316775,RMVar_hsa_circ_60080,RMVar_hsa_circ_193258,RMVar_hsa_circ_193259 2311 RMVar_ID_2311 Human_SNP_ID_660100405 A-to-I Human chr19 + 17177458 17177457 17177458 GCCTCAACCTCCTGGGCTCAAGCAATCCCCCCACCTCAGCCTCCCAAGTAGCTGGGACAACAGGC GCCTCAACCTCCTGGGCTCAAGCAATCCCCCC_CCTCAGCCTCCCAAGTAGCTGGGACAACAGGC CA C MYO9B Ensembl:ENSG00000099331 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1188046130 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_28502,RMVar_hsa_circ_6728,RMVar_hsa_circ_113476,RMVar_hsa_circ_316775,RMVar_hsa_circ_60080,RMVar_hsa_circ_193258,RMVar_hsa_circ_193259 2312 RMVar_ID_2312 Human_SNP_ID_660100408 A-to-I Human chr19 + 17177471 17177471 17177471 GGGCTCAAGCAATCCCCCCACCTCAGCCTCCCAAGTAGCTGGGACAACAGGCACACGCCACCACG GGGCTCAAGCAATCCCCCCACCTCAGCCTCCCGAGTAGCTGGGACAACAGGCACACGCCACCACG A G MYO9B Ensembl:ENSG00000099331 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1009376198 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28502,RMVar_hsa_circ_6728,RMVar_hsa_circ_113476,RMVar_hsa_circ_316775,RMVar_hsa_circ_60080,RMVar_hsa_circ_193258,RMVar_hsa_circ_193259 2313 RMVar_ID_2313 Human_SNP_ID_660100415 A-to-I Human chr19 + 17177491 17177491 17177491 CCTCAGCCTCCCAAGTAGCTGGGACAACAGGCACACGCCACCACGCCTGGCTTATTTTTTCTTTT CCTCAGCCTCCCAAGTAGCTGGGACAACAGGCGCACGCCACCACGCCTGGCTTATTTTTTCTTTT A G MYO9B Ensembl:ENSG00000099331 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1273230931 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28502,RMVar_hsa_circ_6728,RMVar_hsa_circ_113476,RMVar_hsa_circ_316775,RMVar_hsa_circ_60080,RMVar_hsa_circ_193258,RMVar_hsa_circ_193259 2314 RMVar_ID_2314 Human_SNP_ID_660100440 A-to-I Human chr19 + 17177617 17177617 17177617 TTCCCACCTCAGCCTCCCAAAGTGATGGGACTACAGGCATGAGCCACCACACCCAGTCCTCTTTT TTCCCACCTCAGCCTCCCAAAGTGATGGGACTGCAGGCATGAGCCACCACACCCAGTCCTCTTTT A G MYO9B Ensembl:ENSG00000099331 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs544141904 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28502,RMVar_hsa_circ_6728,RMVar_hsa_circ_113476,RMVar_hsa_circ_316775,RMVar_hsa_circ_60080,RMVar_hsa_circ_193258,RMVar_hsa_circ_193259 2315 RMVar_ID_2315 Human_SNP_ID_660101172 A-to-I Human chr19 + 17180215 17180215 17180215 AGATTGCGCCATTGTACTCCAGCCTGGGCGACAGAGTGAGACTCCGTCTCAATAAATAAATAAAT AGATTGCGCCATTGTACTCCAGCCTGGGCGACGGAGTGAGACTCCGTCTCAATAAATAAATAAAT A G MYO9B Ensembl:ENSG00000099331 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1336600667 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28502,RMVar_hsa_circ_6728,RMVar_hsa_circ_113476,RMVar_hsa_circ_316775,RMVar_hsa_circ_60080,RMVar_hsa_circ_193258,RMVar_hsa_circ_193259 2316 RMVar_ID_2316 Human_SNP_ID_660103992 A-to-I Human chr19 + 17190323 17190323 17190323 TCAAGTGATTCTCCTTCCTCAGCCTCTCCAGTACATGGGGTTACAGGCGCCTGCCACCATTCCTG TCAAGTGATTCTCCTTCCTCAGCCTCTCCAGTGCATGGGGTTACAGGCGCCTGCCACCATTCCTG A G MYO9B Ensembl:ENSG00000099331 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs373963046 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28502,RMVar_hsa_circ_113476,RMVar_hsa_circ_193259,RMVar_hsa_circ_301189,RMVar_hsa_circ_193261,RMVar_hsa_circ_264888 2317 RMVar_ID_2317 Human_SNP_ID_660104413 A-to-I Human chr19 + 17191976 17191976 17191976 GAGATCTCATTTCTTTTTTCTTTTTTGTTTTTATTTTTGAGACAGAGTCTTGCTCTGTTGCCCAG GAGATCTCATTTCTTTTTTCTTTTTTGTTTTTTTTTTTGAGACAGAGTCTTGCTCTGTTGCCCAG A T MYO9B Ensembl:ENSG00000099331 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1485003402 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28502,RMVar_hsa_circ_113476,RMVar_hsa_circ_193259,RMVar_hsa_circ_264888 2318 RMVar_ID_2318 Human_SNP_ID_660106598 A-to-I Human chr19 + 17199060 17199060 17199060 TTGTCTCTGCAAAAAAATTTCAAAAATTAGCCAGGCAGGGCGGTGCATGCCTGTAGTCCCAGCTA TTGTCTCTGCAAAAAAATTTCAAAAATTAGCCTGGCAGGGCGGTGCATGCCTGTAGTCCCAGCTA A T MYO9B Ensembl:ENSG00000099331 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1357231864 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28502,RMVar_hsa_circ_113476,RMVar_hsa_circ_193259,RMVar_hsa_circ_76182,RMVar_hsa_circ_118441,RMVar_hsa_circ_305588,RMVar_hsa_circ_193262,RMVar_hsa_circ_193264,RMVar_hsa_circ_193265 2319 RMVar_ID_2319 Human_SNP_ID_660106706 A-to-I Human chr19 + 17199531 17199531 17199531 TTGTTTTTTTGTTTGTTTTTTTTTTGAGACAGAATCTTGCTCTGTTGCCCAGTCTGGCAGTCTGG TTGTTTTTTTGTTTGTTTTTTTTTTGAGACAGTATCTTGCTCTGTTGCCCAGTCTGGCAGTCTGG A T MYO9B Ensembl:ENSG00000099331 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1376304382 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28502,RMVar_hsa_circ_113476,RMVar_hsa_circ_193259,RMVar_hsa_circ_76182,RMVar_hsa_circ_118441,RMVar_hsa_circ_305588,RMVar_hsa_circ_193262,RMVar_hsa_circ_193264,RMVar_hsa_circ_193265 2320 RMVar_ID_2320 Human_SNP_ID_660108906 A-to-I Human chr19 + 17206711 17206711 17206711 AGCTGCCGGAGAAGCAGGAGCAGCTGGCTGCCATCTATGCCGTCCTGGAGCACCTTCCAGAAGCC AGCTGCCGGAGAAGCAGGAGCAGCTGGCTGCCGTCTATGCCGTCCTGGAGCACCTTCCAGAAGCC A G MYO9B Ensembl:ENSG00000099331 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1295454345 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8830381,Human_RBP_ID_9294323 Human_Splice_Rec_1975408,Human_Splice_Rec_1975482,Human_Splice_Rec_1975556,Human_Splice_Rec_1975628,Human_Splice_Rec_1975686 RMVar_hsa_circ_28502,RMVar_hsa_circ_61245,RMVar_hsa_circ_106230,RMVar_hsa_circ_193278,RMVar_hsa_circ_332527 2321 RMVar_ID_2321 Human_SNP_ID_660109170 A-to-I Human chr19 + 17207423 17207423 17207423 GGGAGGCCAAGGCAAGAGGATCACTTGAGGCCAGGAGTTCGAGACCAGCCTGGGCAACATAGCAA GGGAGGCCAAGGCAAGAGGATCACTTGAGGCCGGGAGTTCGAGACCAGCCTGGGCAACATAGCAA A G MYO9B Ensembl:ENSG00000099331 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1055474910 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28502,RMVar_hsa_circ_61245,RMVar_hsa_circ_106230,RMVar_hsa_circ_193278,RMVar_hsa_circ_193279,RMVar_hsa_circ_89936 2322 RMVar_ID_2322 Human_SNP_ID_660117795 A-to-I Human chr19 - 17232829 17232829 17232829 CTGATTTGTTTTTGCAGAGAAGGGATCATACTATGTTGCCCTGGCTGGTCTCAAATCCTGGCCTT CTGATTTGTTTTTGCAGAGAAGGGATCATACTGTGTTGCCCTGGCTGGTCTCAAATCCTGGCCTT T C NR2F6 Ensembl:ENSG00000160113 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs894800323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13390891 RMVar_hsa_circ_109745,RMVar_hsa_circ_111285,RMVar_hsa_circ_112138,RMVar_hsa_circ_193283,RMVar_hsa_circ_193285,RMVar_hsa_circ_193284 2323 RMVar_ID_2323 Human_SNP_ID_660118047 A-to-I Human chr19 - 17233728 17233728 17233728 ACTTTGGGAGGCCGAGGTGGGGAGATTGCTTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACAC ACTTTGGGAGGCCGAGGTGGGGAGATTGCTTGCGGTCAGGAGTTCAAGACCAGCCTGGCCAACAC T G NR2F6 Ensembl:ENSG00000160113 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs947539046 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109745,RMVar_hsa_circ_111285,RMVar_hsa_circ_112138,RMVar_hsa_circ_193283,RMVar_hsa_circ_193285,RMVar_hsa_circ_193284 2324 RMVar_ID_2324 Human_SNP_ID_660118139 A-to-I Human chr19 - 17234075 17234075 17234075 GGGATTACAGGCACGCGTCACCACGCCTGGCTAATTTTTGTGTTTTTAGTAGAGACGGGGTTTCA GGGATTACAGGCACGCGTCACCACGCCTGGCTTATTTTTGTGTTTTTAGTAGAGACGGGGTTTCA T A NR2F6 Ensembl:ENSG00000160113 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1445683655 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109745,RMVar_hsa_circ_111285,RMVar_hsa_circ_112138,RMVar_hsa_circ_193283,RMVar_hsa_circ_193285,RMVar_hsa_circ_193284 2325 RMVar_ID_2325 Human_SNP_ID_660118221 A-to-I Human chr19 - 17234301 17234291 17234301 TGATTTTCCCACTGCACTTGAGCCTGCGCAACAGAGTGAGACCGCGTCTCAAAAATCAATAAATA TGATTTTCCCACTGCACTTGAGCCTGCGCAAC__________CGCGTCTCAAAAATCAATAAATA GGTCTCACTCT G NR2F6 Ensembl:ENSG00000160113 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs904173682 Functional Loss DEL dbSNP153 33..42 33 - - - RMVar_hsa_circ_109745,RMVar_hsa_circ_111285,RMVar_hsa_circ_112138,RMVar_hsa_circ_193283,RMVar_hsa_circ_193285,RMVar_hsa_circ_193284 2326 RMVar_ID_2326 Human_SNP_ID_660118225 A-to-I Human chr19 - 17234301 17234301 17234301 TGATTTTCCCACTGCACTTGAGCCTGCGCAACAGAGTGAGACCGCGTCTCAAAAATCAATAAATA TGATTTTCCCACTGCACTTGAGCCTGCGCAACGGAGTGAGACCGCGTCTCAAAAATCAATAAATA T C NR2F6 Ensembl:ENSG00000160113 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1167831407 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109745,RMVar_hsa_circ_111285,RMVar_hsa_circ_112138,RMVar_hsa_circ_193283,RMVar_hsa_circ_193285,RMVar_hsa_circ_193284 2327 RMVar_ID_2327 Human_SNP_ID_660119732 A-to-I Human chr19 - 17238896 17238895 17238897 CCACCCGGCAGCTTTTTTTATTTTCTAGAGACAGAGTCCCACTATGTTGCCCAGGCTGGTCTCGA CCACCCGGCAGCTTTTTTTATTTTCTAGAGA__GAGTCCCACTATGTTGCCCAGGCTGGTCTCGA CTG C AC010646.1,NR2F6 Ensembl:ENSG00000269095,Ensembl:ENSG00000160113 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277243969 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_13390982 RMVar_hsa_circ_109745,RMVar_hsa_circ_112138,RMVar_hsa_circ_193283,RMVar_hsa_circ_193284 2328 RMVar_ID_2328 Human_SNP_ID_660127331 A-to-I Human chr19 - 17263214 17263214 17263214 AGCCAACATGGTGAAACCCTGTCTCTACTAAAAATACAAAAATTAGCCAGGCGTGGTGGTGGGAG AGCCAACATGGTGAAACCCTGTCTCTACTAAAGATACAAAAATTAGCCAGGCGTGGTGGTGGGAG T C USHBP1 Ensembl:ENSG00000130307 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs968076731 Functional Loss SNV dbSNP153 33..33 33 - - - 2329 RMVar_ID_2329 Human_SNP_ID_660127443 A-to-I Human chr19 - 17263732 17263732 17263732 GAGTAGTTGGGATTACAGGTGTGCGCCACCACATCCGGCTAAGTTTTGCATTTTTAGTGAGACAG GAGTAGTTGGGATTACAGGTGTGCGCCACCACGTCCGGCTAAGTTTTGCATTTTTAGTGAGACAG T C USHBP1 Ensembl:ENSG00000130307 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs553809870 Functional Loss SNV dbSNP153 33..33 33 - - - 2330 RMVar_ID_2330 Human_SNP_ID_660131028 A-to-I Human chr19 + 17275408 17275408 17275408 CACCTCCCGAGTTCAAGCAATTTTCCTGTCTTAGCCTCCCAAGTAGCTGGGATTACAGACATGTG CACCTCCCGAGTTCAAGCAATTTTCCTGTCTTGGCCTCCCAAGTAGCTGGGATTACAGACATGTG A G AC010463.1,BABAM1 Ensembl:ENSG00000269307,Ensembl:ENSG00000105393 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs906045396 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59722,RMVar_hsa_circ_349847,RMVar_hsa_circ_92473,RMVar_hsa_circ_117981,RMVar_hsa_circ_322263,RMVar_hsa_circ_193292,RMVar_hsa_circ_193293,RMVar_hsa_circ_193294,RMVar_hsa_circ_80481,RMVar_hsa_circ_193295 2331 RMVar_ID_2331 Human_SNP_ID_660131032 A-to-I Human chr19 + 17275432 17275432 17275432 CCTGTCTTAGCCTCCCAAGTAGCTGGGATTACAGACATGTGCCATCAGGCCCAGCTAATTTTGTA CCTGTCTTAGCCTCCCAAGTAGCTGGGATTACGGACATGTGCCATCAGGCCCAGCTAATTTTGTA A G AC010463.1,BABAM1 Ensembl:ENSG00000269307,Ensembl:ENSG00000105393 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1490332108 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59722,RMVar_hsa_circ_349847,RMVar_hsa_circ_92473,RMVar_hsa_circ_117981,RMVar_hsa_circ_322263,RMVar_hsa_circ_193292,RMVar_hsa_circ_193293,RMVar_hsa_circ_193294,RMVar_hsa_circ_80481,RMVar_hsa_circ_193295 2332 RMVar_ID_2332 Human_SNP_ID_660131039 A-to-I Human chr19 + 17275473 17275473 17275473 CCATCAGGCCCAGCTAATTTTGTATTTTTAGTAGAGACAGGGTTTCACCGTGTTGGCCAGGCTGG CCATCAGGCCCAGCTAATTTTGTATTTTTAGTGGAGACAGGGTTTCACCGTGTTGGCCAGGCTGG A G AC010463.1,BABAM1 Ensembl:ENSG00000269307,Ensembl:ENSG00000105393 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1265827348 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59722,RMVar_hsa_circ_349847,RMVar_hsa_circ_92473,RMVar_hsa_circ_117981,RMVar_hsa_circ_322263,RMVar_hsa_circ_193292,RMVar_hsa_circ_193293,RMVar_hsa_circ_193294,RMVar_hsa_circ_80481,RMVar_hsa_circ_193295 2333 RMVar_ID_2333 Human_SNP_ID_660131051 A-to-I Human chr19 + 17275524 17275524 17275524 GTTGGCCAGGCTGGCCTCGAACTCCTGACCTCAGATGGTCCACCCGCCTTGGCCTCCCAAAGTGC GTTGGCCAGGCTGGCCTCGAACTCCTGACCTCGGATGGTCCACCCGCCTTGGCCTCCCAAAGTGC A G AC010463.1,BABAM1 Ensembl:ENSG00000269307,Ensembl:ENSG00000105393 Protein coding,Protein coding intron,intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs946665560 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59722,RMVar_hsa_circ_349847,RMVar_hsa_circ_92473,RMVar_hsa_circ_117981,RMVar_hsa_circ_322263,RMVar_hsa_circ_193292,RMVar_hsa_circ_193293,RMVar_hsa_circ_193294,RMVar_hsa_circ_80481,RMVar_hsa_circ_193295 2334 RMVar_ID_2334 Human_SNP_ID_660131057 A-to-I Human chr19 + 17275533 17275530 17275533 GCTGGCCTCGAACTCCTGACCTCAGATGGTCCACCCGCCTTGGCCTCCCAAAGTGCTATGATTGC GCTGGCCTCGAACTCCTGACCTCAGATGGT___CCCGCCTTGGCCTCCCAAAGTGCTATGATTGC TCCA T AC010463.1,BABAM1 Ensembl:ENSG00000269307,Ensembl:ENSG00000105393 Protein coding,Protein coding intron,intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1407210061 Functional Loss DEL dbSNP153 31..33 33 - - - RMVar_hsa_circ_59722,RMVar_hsa_circ_349847,RMVar_hsa_circ_92473,RMVar_hsa_circ_117981,RMVar_hsa_circ_322263,RMVar_hsa_circ_193292,RMVar_hsa_circ_193293,RMVar_hsa_circ_193294,RMVar_hsa_circ_80481,RMVar_hsa_circ_193295 2335 RMVar_ID_2335 Human_SNP_ID_660131058 A-to-I Human chr19 + 17275533 17275533 17275533 GCTGGCCTCGAACTCCTGACCTCAGATGGTCCACCCGCCTTGGCCTCCCAAAGTGCTATGATTGC GCTGGCCTCGAACTCCTGACCTCAGATGGTCCGCCCGCCTTGGCCTCCCAAAGTGCTATGATTGC A G AC010463.1,BABAM1 Ensembl:ENSG00000269307,Ensembl:ENSG00000105393 Protein coding,Protein coding intron,intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs547278941 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59722,RMVar_hsa_circ_349847,RMVar_hsa_circ_92473,RMVar_hsa_circ_117981,RMVar_hsa_circ_322263,RMVar_hsa_circ_193292,RMVar_hsa_circ_193293,RMVar_hsa_circ_193294,RMVar_hsa_circ_80481,RMVar_hsa_circ_193295 2336 RMVar_ID_2336 Human_SNP_ID_660131059 A-to-I Human chr19 + 17275533 17275533 17275533 GCTGGCCTCGAACTCCTGACCTCAGATGGTCCACCCGCCTTGGCCTCCCAAAGTGCTATGATTGC GCTGGCCTCGAACTCCTGACCTCAGATGGTCCTCCCGCCTTGGCCTCCCAAAGTGCTATGATTGC A T AC010463.1,BABAM1 Ensembl:ENSG00000269307,Ensembl:ENSG00000105393 Protein coding,Protein coding intron,intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs547278941 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59722,RMVar_hsa_circ_349847,RMVar_hsa_circ_92473,RMVar_hsa_circ_117981,RMVar_hsa_circ_322263,RMVar_hsa_circ_193292,RMVar_hsa_circ_193293,RMVar_hsa_circ_193294,RMVar_hsa_circ_80481,RMVar_hsa_circ_193295 2337 RMVar_ID_2337 Human_SNP_ID_660131648 A-to-I Human chr19 + 17277319 17277319 17277319 TGCCTCCCGGGTTCAAGCAATTCTCCTGTGTCAGCCTCCCGAGTAGCTGGGGTTACAGGTACCTG TGCCTCCCGGGTTCAAGCAATTCTCCTGTGTCCGCCTCCCGAGTAGCTGGGGTTACAGGTACCTG A C AC010463.1,BABAM1 Ensembl:ENSG00000269307,Ensembl:ENSG00000105393 Protein coding,Protein coding intron,intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs772593135 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_515597 Human_Splice_Rec_1976096,Human_Splice_Rec_1976097 RMVar_hsa_circ_92473,RMVar_hsa_circ_193294,RMVar_hsa_circ_115721,RMVar_hsa_circ_193299 2338 RMVar_ID_2338 Human_SNP_ID_660131794 A-to-I Human chr19 + 17277899 17277899 17277899 GAGACCCTGTGTCAAAAAATAAAAATACGGCCAGGTGTGGTGGCTCACACCTGTAATCCCAGCAC GAGACCCTGTGTCAAAAAATAAAAATACGGCCGGGTGTGGTGGCTCACACCTGTAATCCCAGCAC A G AC010463.1,BABAM1 Ensembl:ENSG00000269307,Ensembl:ENSG00000105393 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1403445563 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115721,RMVar_hsa_circ_193299 2339 RMVar_ID_2339 Human_SNP_ID_660131992 A-to-I Human chr19 + 17278516 17278516 17278516 ATTTTTTAGTAGAGACGGGGTTTCACTGTGTTAGCCAGGATGGTCTTGATCTCCTGACCTTGTGA ATTTTTTAGTAGAGACGGGGTTTCACTGTGTTGGCCAGGATGGTCTTGATCTCCTGACCTTGTGA A G AC010463.1,BABAM1 Ensembl:ENSG00000269307,Ensembl:ENSG00000105393 Protein coding,Protein coding intron,intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1054868141 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115721,RMVar_hsa_circ_193299 2340 RMVar_ID_2340 Human_SNP_ID_660132016 A-to-I Human chr19 + 17278561 17278561 17278561 TTGATCTCCTGACCTTGTGATCTGCCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG TTGATCTCCTGACCTTGTGATCTGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG A G AC010463.1,BABAM1 Ensembl:ENSG00000269307,Ensembl:ENSG00000105393 Protein coding,Protein coding intron,intron GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829 ASD brains,Fragile X samples from UC Davis FXTAS brain repository;Bronchiolar epithelium,BEP2D cell line - 30559470,31158229 RNA-Seq:(High) rs530634476 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115721,RMVar_hsa_circ_193299 2341 RMVar_ID_2341 Human_SNP_ID_660132017 A-to-I Human chr19 + 17278561 17278561 17278561 TTGATCTCCTGACCTTGTGATCTGCCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG TTGATCTCCTGACCTTGTGATCTGCCCGCCTCTGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG A T AC010463.1,BABAM1 Ensembl:ENSG00000269307,Ensembl:ENSG00000105393 Protein coding,Protein coding intron,intron GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829 ASD brains,Fragile X samples from UC Davis FXTAS brain repository;Bronchiolar epithelium,BEP2D cell line - 30559470,31158229 RNA-Seq:(High) rs530634476 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115721,RMVar_hsa_circ_193299 2342 RMVar_ID_2342 Human_SNP_ID_660134153 A-to-I Human chr19 + 17284477 17284477 17284477 GCCGTCTCGGCTCACTGCAACCTCCACCTCCCAGGTTCAAACAATCCTCTTGTCTCAGCCTCTCA GCCGTCTCGGCTCACTGCAACCTCCACCTCCCGGGTTCAAACAATCCTCTTGTCTCAGCCTCTCA A G ANKLE1 Ensembl:ENSG00000160117 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1353020667 Functional Loss SNV dbSNP153 33..33 33 - - - 2343 RMVar_ID_2343 Human_SNP_ID_660135033 A-to-I Human chr19 + 17286746 17286744 17286746 AGGGAGCACCCAGGCAGATCTCCCCCAGGCTGAGAGAGGACTTTGTTACAGATGGTACTGCTGGA AGGGAGCACCCAGGCAGATCTCCCCCAGGCT__GAGAGGACTTTGTTACAGATGGTACTGCTGGA TGA T ANKLE1 Ensembl:ENSG00000160117 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs928797142 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_5292734,Human_RBP_ID_5649964,Human_RBP_ID_6725931,Human_RBP_ID_13391260,Human_RBP_ID_17272080,Human_RBP_ID_23813189 2344 RMVar_ID_2344 Human_SNP_ID_660138114 A-to-I Human chr19 + 17296836 17296836 17296836 CCTGTCTCAGCCTCCCGAGTAGCTGGGATTACAGGCATCTGCCATTATGCCCGGCTAATTTTTGT CCTGTCTCAGCCTCCCGAGTAGCTGGGATTACGGGCATCTGCCATTATGCCCGGCTAATTTTTGT A G MRPL34 Ensembl:ENSG00000130312 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs954182918 Functional Loss SNV dbSNP153 33..33 33 - - - 2345 RMVar_ID_2345 Human_SNP_ID_660138478 A-to-I Human chr19 - 17298136 17298136 17298136 AGGCGGGCGGATCAGGAGGTCAGGAGATCAAGACCATCCTGGCTAACACGGTGAAACCCCGTCTC AGGCGGGCGGATCAGGAGGTCAGGAGATCAAGCCCATCCTGGCTAACACGGTGAAACCCCGTCTC T G ABHD8 Ensembl:ENSG00000127220 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs564413263 Functional Loss SNV dbSNP153 33..33 33 - - - 2346 RMVar_ID_2346 Human_SNP_ID_660146766 A-to-I Human chr19 - 17324096 17324096 17324096 CCATAGGTCAGAAGCCAGAGGGACTTCCTCAAACTGTCCTCCCCCTGTGACCGGCAGGGCCGTGC CCATAGGTCAGAAGCCAGAGGGACTTCCTCAAGCTGTCCTCCCCCTGTGACCGGCAGGGCCGTGC T C ANO8 Ensembl:ENSG00000074855 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs541916755 Functional Loss SNV dbSNP153 33..33 33 - - - 2347 RMVar_ID_2347 Human_SNP_ID_660168373 A-to-I Human chr19 - 17393505 17393505 17393505 GAACGCCTGTAATCCCAGCTCCTCAGGAGGCTAACGCGGGAGAATCGCTTGAACCCGGAAGGTGG GAACGCCTGTAATCCCAGCTCCTCAGGAGGCTTACGCGGGAGAATCGCTTGAACCCGGAAGGTGG T A CCDC194 Ensembl:ENSG00000269720 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1568382381 Functional Loss SNV dbSNP153 33..33 33 - - - 2348 RMVar_ID_2348 Human_SNP_ID_660169489 A-to-I Human chr19 - 17397589 17397589 17397589 TGGCCTCGTGATTCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCAGCTCGC TGGCCTCGTGATTCGCCCGCCTCGGCCTCCCAGAGTGCTGGGATTACAGGCATGAGCCAGCTCGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1356943325 Functional Loss SNV dbSNP153 33..33 33 - - - 2349 RMVar_ID_2349 Human_SNP_ID_660169539 A-to-I Human chr19 - 17397731 17397730 17397732 CTGCCTCCCGGGTTCAAGCGATTCTCCGTCTCAGTCTCCCGAGTAGCTGGGATTACAGGTGCCCG CTGCCTCCCGGGTTCAAGCGATTCTCCGTCT__GTCTCCCGAGTAGCTGGGATTACAGGTGCCCG CTG C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs578025504 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_6726121 2350 RMVar_ID_2350 Human_SNP_ID_660170253 A-to-I Human chr19 - 17400536 17400536 17400536 CTGCAAACTCCGTCTCCCGGGTTCAAGTGATTATCCTGCCTCAGCCTCCCGAGTAGCTGGGATTA CTGCAAACTCCGTCTCCCGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTA T G - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1012477616 Functional Loss SNV dbSNP153 33..33 33 - - - 2351 RMVar_ID_2351 Human_SNP_ID_660170272 A-to-I Human chr19 - 17400612 17400612 17400612 TTTTTTTGTTTGTTTTTTTGAGATGGAGTCTCACTCTGTCTCCCAGGCTGGAGTGCAGTGGTGCG TTTTTTTGTTTGTTTTTTTGAGATGGAGTCTCGCTCTGTCTCCCAGGCTGGAGTGCAGTGGTGCG T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1568383965 Functional Loss SNV dbSNP153 33..33 33 - - - 2352 RMVar_ID_2352 Human_SNP_ID_660170372 A-to-I Human chr19 - 17401022 17401022 17401022 CCAGGAGGTGGAGGTTGCAGTGAGCTGAGATCACGCTACTGCACTCTAGCCTGGGCGACAGAGCA CCAGGAGGTGGAGGTTGCAGTGAGCTGAGATCCCGCTACTGCACTCTAGCCTGGGCGACAGAGCA T G - - Other Unknown GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1411039222 Functional Loss SNV dbSNP153 33..33 33 - - - 2353 RMVar_ID_2353 Human_SNP_ID_660170465 A-to-I Human chr19 - 17401305 17401305 17401305 CATCCTGGCGAACACGGTGAAACCCTGTCTCTACTAAAAATACAAAAAATTAGCCTGGCGTGGTG CATCCTGGCGAACACGGTGAAACCCTGTCTCTTCTAAAAATACAAAAAATTAGCCTGGCGTGGTG T A - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1215049480 Functional Loss SNV dbSNP153 33..33 33 - - - 2354 RMVar_ID_2354 Human_SNP_ID_660170466 A-to-I Human chr19 - 17401305 17401305 17401305 CATCCTGGCGAACACGGTGAAACCCTGTCTCTACTAAAAATACAAAAAATTAGCCTGGCGTGGTG CATCCTGGCGAACACGGTGAAACCCTGTCTCTGCTAAAAATACAAAAAATTAGCCTGGCGTGGTG T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1215049480 Functional Loss SNV dbSNP153 33..33 33 - - - 2355 RMVar_ID_2355 Human_SNP_ID_660170637 A-to-I Human chr19 - 17401937 17401937 17401937 GCCTCAAACTCCTGACCTCAAGGGATCTACCCACCTTGGGCTCCTAAAGTGCTGGGATTACAGGC GCCTCAAACTCCTGACCTCAAGGGATCTACCCGCCTTGGGCTCCTAAAGTGCTGGGATTACAGGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1211264292 Functional Loss SNV dbSNP153 33..33 33 - - - 2356 RMVar_ID_2356 Human_SNP_ID_660172918 A-to-I Human chr19 + 17409671 17409671 17409671 TTAGGTTTCTCCATGTTGGCCAGGCTGGTCTCAAACTCCCGACCTCAGGTGATCTGCCCGCCTCG TTAGGTTTCTCCATGTTGGCCAGGCTGGTCTCGAACTCCCGACCTCAGGTGATCTGCCCGCCTCG A G BISPR,MVB12A Ensembl:ENSG00000282851,Ensembl:ENSG00000141971 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1221664539 Functional Loss SNV dbSNP153 33..33 33 - - - 2357 RMVar_ID_2357 Human_SNP_ID_660172981 A-to-I Human chr19 + 17409858 17409858 17409858 ACTGCAACCTCTGACCTCCGCCTCCTGGGTTCAAGCAATCCTGCTGCCTCAGTCTCCTGAGTAGC ACTGCAACCTCTGACCTCCGCCTCCTGGGTTCGAGCAATCCTGCTGCCTCAGTCTCCTGAGTAGC A G BISPR,MVB12A Ensembl:ENSG00000282851,Ensembl:ENSG00000141971 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs929789772 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8479484 2358 RMVar_ID_2358 Human_SNP_ID_660174238 A-to-I Human chr19 + 17414103 17414103 17414103 AGGACTTCGAGAACAGCCTGGACAAAATGGTGAAACCCTGTCTCTACTGAAAATACAAAAATTAG AGGACTTCGAGAACAGCCTGGACAAAATGGTGTAACCCTGTCTCTACTGAAAATACAAAAATTAG A T BISPR,MVB12A Ensembl:ENSG00000282851,Ensembl:ENSG00000141971 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1186731828 Functional Loss SNV dbSNP153 33..33 33 - - - 2359 RMVar_ID_2359 Human_SNP_ID_660174676 A-to-I Human chr19 + 17415791 17415790 17415792 CGCTTGGGTATAACACTTTGAGCCTGCGAGGCAGAGTTTGCAGTGAGCCGAGATCACGCCACTGC CGCTTGGGTATAACACTTTGAGCCTGCGAGGC__AGTTTGCAGTGAGCCGAGATCACGCCACTGC CAG C BISPR,MVB12A Ensembl:ENSG00000282851,Ensembl:ENSG00000141971 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1419978241 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_8839207 2360 RMVar_ID_2360 Human_SNP_ID_660176488 A-to-I Human chr19 + 17421367 17421367 17421367 CCACCACGCCTGGCTAATTTTGTATTTTTAGTAGAGACGGGGTTTCTCCATGTTGGTCAGGCTGG CCACCACGCCTGGCTAATTTTGTATTTTTAGTTGAGACGGGGTTTCTCCATGTTGGTCAGGCTGG A T MVB12A Ensembl:ENSG00000141971 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1193951304 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69057,RMVar_hsa_circ_193319,RMVar_hsa_circ_17678,RMVar_hsa_circ_54762,RMVar_hsa_circ_106633 2361 RMVar_ID_2361 Human_SNP_ID_660190225 A-to-I Human chr19 - 17468244 17468244 17468244 CAGAGGATCCAGTGAGCCGAGATCGCGTCACTATACTCCAGCCTGGGTGACAAAGCAAGACCCTG CAGAGGATCCAGTGAGCCGAGATCGCGTCACTGTACTCCAGCCTGGGTGACAAAGCAAGACCCTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs930939818 Functional Loss SNV dbSNP153 33..33 33 - - - 2362 RMVar_ID_2362 Human_SNP_ID_660191632 A-to-I Human chr19 + 17473107 17473106 17473107 GGTGCACACCACCACACCTGGCTAATTTTTTTATTTTTTGTAGAGACGTGGTTCTGCCACGTTGC GGTGCACACCACCACACCTGGCTAATTTTTTT_TTTTTTGTAGAGACGTGGTTCTGCCACGTTGC TA T SLC27A1 Ensembl:ENSG00000130304 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1267282630 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_13392417 2363 RMVar_ID_2363 Human_SNP_ID_660194805 A-to-I Human chr19 + 17484821 17484821 17484821 CACTGTGAACATTTTGGGGGGTGTGAGCAGCCATTGCAGGGATCTGGGGAGGCCTGGGAAAGGCA CACTGTGAACATTTTGGGGGGTGTGAGCAGCCGTTGCAGGGATCTGGGGAGGCCTGGGAAAGGCA A G SLC27A1 Ensembl:ENSG00000130304 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs529748676 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3583306 2364 RMVar_ID_2364 Human_SNP_ID_660198021 A-to-I Human chr19 + 17495361 17495361 17495361 TGGAGTGCAGTGGCGCGATCTCGGCCCACTGCAAGCTCCGCCTCCCGGGTTTACGCCATTCTCCT TGGAGTGCAGTGGCGCGATCTCGGCCCACTGCGAGCTCCGCCTCCCGGGTTTACGCCATTCTCCT A G SLC27A1 Ensembl:ENSG00000130304 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1211449199 Functional Loss SNV dbSNP153 33..33 33 - - - 2365 RMVar_ID_2365 Human_SNP_ID_660198752 A-to-I Human chr19 + 17497833 17497832 17497834 CGTGCTGTTATTTTGTTGTTGTTGTTTGAGACAGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCA CGTGCTGTTATTTTGTTGTTGTTGTTTGAGAC__AGTCTCGCTCTGTCGCCCAGGCTGGAGTGCA CAG C SLC27A1 Ensembl:ENSG00000130304 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs774624845 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_5192987 RMVar_hsa_circ_9031,RMVar_hsa_circ_120682,RMVar_hsa_circ_330842,RMVar_hsa_circ_111506,RMVar_hsa_circ_193323,RMVar_hsa_circ_193324 2366 RMVar_ID_2366 Human_SNP_ID_660198753 A-to-I Human chr19 + 17497833 17497833 17497833 CGTGCTGTTATTTTGTTGTTGTTGTTTGAGACAGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCA CGTGCTGTTATTTTGTTGTTGTTGTTTGAGACTGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCA A T SLC27A1 Ensembl:ENSG00000130304 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006033733 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5192987 RMVar_hsa_circ_9031,RMVar_hsa_circ_120682,RMVar_hsa_circ_330842,RMVar_hsa_circ_111506,RMVar_hsa_circ_193323,RMVar_hsa_circ_193324 2367 RMVar_ID_2367 Human_SNP_ID_660200538 A-to-I Human chr19 - 17503598 17503598 17503598 TAAATTAGCTGGGTGTCATGGCACGTGCGTGTAGTTCCGGCTACTTGGGAGGCTGAGGTGGGAGA TAAATTAGCTGGGTGTCATGGCACGTGCGTGTGGTTCCGGCTACTTGGGAGGCTGAGGTGGGAGA T C AC010618.3 Ensembl:ENSG00000269439 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978412726 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1977144 2368 RMVar_ID_2368 Human_SNP_ID_660203647 A-to-I Human chr19 + 17513135 17513135 17513135 AGTTTTGGCCGGGTGCGGTGGCTCACGCGTGTAATCCCAGCACTTTGGGAGGCCGACGTGAGTAG AGTTTTGGCCGGGTGCGGTGGCTCACGCGTGTTATCCCAGCACTTTGGGAGGCCGACGTGAGTAG A T PGLS Ensembl:ENSG00000130313 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1321976155 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193325,RMVar_hsa_circ_80786 2369 RMVar_ID_2369 Human_SNP_ID_660204162 A-to-I Human chr19 + 17515063 17515063 17515063 GTCCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGCCGTGAGCCACCATGCCTGGCCATTTTCT GTCCCACCTCAGCCTCCCAAAGTGCTGGGATTTCAGCCGTGAGCCACCATGCCTGGCCATTTTCT A T PGLS Ensembl:ENSG00000130313 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1342186509 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193325,RMVar_hsa_circ_80786 2370 RMVar_ID_2370 Human_SNP_ID_660214862 A-to-I Human chr19 + 17552178 17552178 17552178 TCGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGC TCGGCTCACTGCAACCTCCGCCTCCCGGGTTCGAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGC A G NIBAN3 Ensembl:ENSG00000167483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs919588341 Functional Loss SNV dbSNP153 33..33 33 - - - 2371 RMVar_ID_2371 Human_SNP_ID_660214915 A-to-I Human chr19 + 17552401 17552401 17552401 ACACGTGGCCTAATTTTTTTTTTTTAAATAATAGAGACAAGGTCTCGCTATGCTGCCCAGGCTGA ACACGTGGCCTAATTTTTTTTTTTTAAATAATGGAGACAAGGTCTCGCTATGCTGCCCAGGCTGA A G NIBAN3 Ensembl:ENSG00000167483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1315768642 Functional Loss SNV dbSNP153 33..33 33 - - - 2372 RMVar_ID_2372 Human_SNP_ID_660214975 A-to-I Human chr19 + 17552681 17552681 17552681 GGCCAGGCGTGGCAGTGCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGCAGATCACT GGCCAGGCGTGGCAGTGCACACCTGTAATCCCGGCACTTTGGGAGGCTGAGGCGGGCAGATCACT A G NIBAN3 Ensembl:ENSG00000167483 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs965560167 Functional Loss SNV dbSNP153 33..33 33 - - - 2373 RMVar_ID_2373 Human_SNP_ID_660214986 A-to-I Human chr19 + 17552729 17552729 17552729 GAGGCGGGCAGATCACTTGAGCTCAGGAGTTCAAGACCAGCCTGGCGAACATAGTGAGACCTCAT GAGGCGGGCAGATCACTTGAGCTCAGGAGTTCGAGACCAGCCTGGCGAACATAGTGAGACCTCAT A G NIBAN3 Ensembl:ENSG00000167483 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs912369929 Functional Loss SNV dbSNP153 33..33 33 - - - 2374 RMVar_ID_2374 Human_SNP_ID_660215007 A-to-I Human chr19 + 17552818 17552818 17552818 GGCCGGGAGTGGTGGCTCACGCCTGTCATCCCAGCACTTTGGGAGGCTGAGACAGGTGGATTGCT GGCCGGGAGTGGTGGCTCACGCCTGTCATCCCGGCACTTTGGGAGGCTGAGACAGGTGGATTGCT A G NIBAN3 Ensembl:ENSG00000167483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs367662415 Functional Loss SNV dbSNP153 33..33 33 - - - 2375 RMVar_ID_2375 Human_SNP_ID_660216261 A-to-I Human chr19 + 17556806 17556806 17556806 GCGGTGGTGTGTGCCTGTAGTCCCAGCTATTCAGGAGGCTGACGCAGGAGAATCGCTTGAGCCCA GCGGTGGTGTGTGCCTGTAGTCCCAGCTATTCCGGAGGCTGACGCAGGAGAATCGCTTGAGCCCA A C COLGALT1 Ensembl:ENSG00000130309 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs997827281 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107345,RMVar_hsa_circ_193333 2376 RMVar_ID_2376 Human_SNP_ID_660216280 A-to-I Human chr19 + 17556854 17556854 17556854 AGAATCGCTTGAGCCCAGGAGTTCGAGGCTGCAGTGACCTATGATTGCACCACTGCACTCCAGCC AGAATCGCTTGAGCCCAGGAGTTCGAGGCTGCCGTGACCTATGATTGCACCACTGCACTCCAGCC A C COLGALT1 Ensembl:ENSG00000130309 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1279521769 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25388900 RMVar_hsa_circ_107345,RMVar_hsa_circ_193333 2377 RMVar_ID_2377 Human_SNP_ID_660216412 A-to-I Human chr19 + 17557355 17557355 17557355 ACGGAATCTTGCTCTGTCGCCCAGGCTGGAGTACAGTGACACGATCTCAGCTCATTGCAACCTCC ACGGAATCTTGCTCTGTCGCCCAGGCTGGAGTCCAGTGACACGATCTCAGCTCATTGCAACCTCC A C COLGALT1 Ensembl:ENSG00000130309 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1471563048 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107345,RMVar_hsa_circ_193333 2378 RMVar_ID_2378 Human_SNP_ID_660216530 A-to-I Human chr19 + 17557804 17557804 17557804 TTGTATTTTTTCTAGAGATGGGGTTTTGCCCTATTGGCCAGGCTGGTCTCGAACTCCCGAGCTCA TTGTATTTTTTCTAGAGATGGGGTTTTGCCCTGTTGGCCAGGCTGGTCTCGAACTCCCGAGCTCA A G COLGALT1 Ensembl:ENSG00000130309 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs879865242 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25388905 RMVar_hsa_circ_107345,RMVar_hsa_circ_193333 2379 RMVar_ID_2379 Human_SNP_ID_660216862 A-to-I Human chr19 + 17558927 17558927 17558927 CACGCTTGTTAAGTCCAGCACTTTGGGAGGCCAAGGTGGGCGGATCACGAGGTCAGGAGATCGAG CACGCTTGTTAAGTCCAGCACTTTGGGAGGCCGAGGTGGGCGGATCACGAGGTCAGGAGATCGAG A G COLGALT1 Ensembl:ENSG00000130309 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs547738919 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107345,RMVar_hsa_circ_193333 2380 RMVar_ID_2380 Human_SNP_ID_660216868 A-to-I Human chr19 + 17558941 17558941 17558941 CCAGCACTTTGGGAGGCCAAGGTGGGCGGATCACGAGGTCAGGAGATCGAGACCAGCCTGGCCAA CCAGCACTTTGGGAGGCCAAGGTGGGCGGATCGCGAGGTCAGGAGATCGAGACCAGCCTGGCCAA A G COLGALT1 Ensembl:ENSG00000130309 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1381729261 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107345,RMVar_hsa_circ_193333 2381 RMVar_ID_2381 Human_SNP_ID_660218736 A-to-I Human chr19 + 17565255 17565255 17565255 TCGGCTCACTGCAACCTCCATCTCCTGGGTTCAAGCGATTCTCCTGCGTTAGTCTCCCGAGTAGC TCGGCTCACTGCAACCTCCATCTCCTGGGTTCGAGCGATTCTCCTGCGTTAGTCTCCCGAGTAGC A G COLGALT1 Ensembl:ENSG00000130309 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1283352744 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 2382 RMVar_ID_2382 Human_SNP_ID_660218937 A-to-I Human chr19 + 17566093 17566093 17566093 GCAGTAAAAGAAAAAAAATCCAGACCGGGCACAATGGCTCACACCTGTAATCCCAGCACTTTGGG GCAGTAAAAGAAAAAAAATCCAGACCGGGCACTATGGCTCACACCTGTAATCCCAGCACTTTGGG A T COLGALT1 Ensembl:ENSG00000130309 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1358277472 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1977495 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 2383 RMVar_ID_2383 Human_SNP_ID_660223886 A-to-I Human chr19 + 17582723 17582723 17582723 TTCCTGTACCCTCGGTCGTCTGAGCTGTGTGCAGACAACATCCCCCCACCACCCAAGAGGGAGGG TTCCTGTACCCTCGGTCGTCTGAGCTGTGTGCCGACAACATCCCCCCACCACCCAAGAGGGAGGG A C COLGALT1 Ensembl:ENSG00000130309 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs140485177 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_515874,Human_RBP_ID_5117395,Human_RBP_ID_5146247,Human_RBP_ID_8198684,Human_RBP_ID_13392652,Human_RBP_ID_17656877,Human_RBP_ID_22231337,Human_RBP_ID_23210891,Human_RBP_ID_23786250,Human_RBP_ID_26472219,Human_RBP_ID_26770011,Human_RBP_ID_27465169 Human_miRNA_ID_1009359,Human_miRNA_ID_2653676,Human_miRNA_ID_2754874 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 2384 RMVar_ID_2384 Human_SNP_ID_660223887 A-to-I Human chr19 + 17582723 17582723 17582723 TTCCTGTACCCTCGGTCGTCTGAGCTGTGTGCAGACAACATCCCCCCACCACCCAAGAGGGAGGG TTCCTGTACCCTCGGTCGTCTGAGCTGTGTGCGGACAACATCCCCCCACCACCCAAGAGGGAGGG A G COLGALT1 Ensembl:ENSG00000130309 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs140485177 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_515874,Human_RBP_ID_5117395,Human_RBP_ID_5146247,Human_RBP_ID_8198684,Human_RBP_ID_13392652,Human_RBP_ID_17656877,Human_RBP_ID_22231337,Human_RBP_ID_23210891,Human_RBP_ID_23786250,Human_RBP_ID_26472219,Human_RBP_ID_26770011,Human_RBP_ID_27465169 Human_miRNA_ID_1009359,Human_miRNA_ID_2653676,Human_miRNA_ID_2754874 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 2385 RMVar_ID_2385 Human_SNP_ID_660233006 A-to-I Human chr19 - 17614102 17614102 17614102 ACTCAGGAGGCTGAGGCAGGAGAATCGCTTTAACCTGGGAGGCGGAGGTTGCAGTGAGCCGAGAT ACTCAGGAGGCTGAGGCAGGAGAATCGCTTTACCCTGGGAGGCGGAGGTTGCAGTGAGCCGAGAT T G UNC13A Ensembl:ENSG00000130477 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1043499522 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111703,RMVar_hsa_circ_268988,RMVar_hsa_circ_265419,RMVar_hsa_circ_193354 2386 RMVar_ID_2386 Human_SNP_ID_660264719 A-to-I Human chr19 + 17726960 17726958 17726961 CTGAGAAAGAAGCCAAGACCCCCCGGGAGTTGAAGAAAGACCCCAAACCGAGTGTCTCCCGGACC CTGAGAAAGAAGCCAAGACCCCCCGGGAGTT___GAAAGACCCCAAACCGAGTGTCTCCCGGACC TGAA T MAP1S Ensembl:ENSG00000130479 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749736504 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_8479567,Human_RBP_ID_26817207 RMVar_hsa_circ_10143,RMVar_hsa_circ_46934,RMVar_hsa_circ_193373,RMVar_hsa_circ_106091 2387 RMVar_ID_2387 Human_SNP_ID_660276124 A-to-I Human chr19 + 17767431 17767431 17767431 AAAAAAAAAACACCCAAAACTACCCAGGCATGATGGCACATGCCGGTAGTCCCAGCTACTCAGGA AAAAAAAAAACACCCAAAACTACCCAGGCATGCTGGCACATGCCGGTAGTCCCAGCTACTCAGGA A C FCHO1 Ensembl:ENSG00000130475 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2081073 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81082,RMVar_hsa_circ_193376,RMVar_hsa_circ_122521,RMVar_hsa_circ_100852,RMVar_hsa_circ_193380,RMVar_hsa_circ_193382,RMVar_hsa_circ_41081 2388 RMVar_ID_2388 Human_SNP_ID_660276125 A-to-I Human chr19 + 17767431 17767431 17767431 AAAAAAAAAACACCCAAAACTACCCAGGCATGATGGCACATGCCGGTAGTCCCAGCTACTCAGGA AAAAAAAAAACACCCAAAACTACCCAGGCATGGTGGCACATGCCGGTAGTCCCAGCTACTCAGGA A G FCHO1 Ensembl:ENSG00000130475 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2081073 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81082,RMVar_hsa_circ_193376,RMVar_hsa_circ_122521,RMVar_hsa_circ_100852,RMVar_hsa_circ_193380,RMVar_hsa_circ_193382,RMVar_hsa_circ_41081 2389 RMVar_ID_2389 Human_SNP_ID_660276126 A-to-I Human chr19 + 17767431 17767431 17767431 AAAAAAAAAACACCCAAAACTACCCAGGCATGATGGCACATGCCGGTAGTCCCAGCTACTCAGGA AAAAAAAAAACACCCAAAACTACCCAGGCATGTTGGCACATGCCGGTAGTCCCAGCTACTCAGGA A T FCHO1 Ensembl:ENSG00000130475 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2081073 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81082,RMVar_hsa_circ_193376,RMVar_hsa_circ_122521,RMVar_hsa_circ_100852,RMVar_hsa_circ_193380,RMVar_hsa_circ_193382,RMVar_hsa_circ_41081 2390 RMVar_ID_2390 Human_SNP_ID_660276146 A-to-I Human chr19 + 17767522 17767522 17767522 ATGGGAGGTCGAGGCTGCAGTGAGCCATGATCATGCCACTGCACTCCAGCCTAGGCAACAGAGAA ATGGGAGGTCGAGGCTGCAGTGAGCCATGATCTTGCCACTGCACTCCAGCCTAGGCAACAGAGAA A T FCHO1 Ensembl:ENSG00000130475 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1472226119 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81082,RMVar_hsa_circ_193376,RMVar_hsa_circ_122521,RMVar_hsa_circ_100852,RMVar_hsa_circ_193380,RMVar_hsa_circ_193382,RMVar_hsa_circ_41081 2391 RMVar_ID_2391 Human_SNP_ID_660276325 A-to-I Human chr19 + 17768132 17768132 17768132 CTCTGTTGCCCAGGCTGGAGTGCAGTGTGCACAATCTCAGCTCACTGCAATCTCCATCTCTTGGG CTCTGTTGCCCAGGCTGGAGTGCAGTGTGCACTATCTCAGCTCACTGCAATCTCCATCTCTTGGG A T FCHO1 Ensembl:ENSG00000130475 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs950762717 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81082,RMVar_hsa_circ_193376,RMVar_hsa_circ_122521,RMVar_hsa_circ_100852,RMVar_hsa_circ_193380,RMVar_hsa_circ_193382,RMVar_hsa_circ_41081 2392 RMVar_ID_2392 Human_SNP_ID_660276333 A-to-I Human chr19 + 17768168 17768168 17768168 TCAGCTCACTGCAATCTCCATCTCTTGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCAGGTAGT TCAGCTCACTGCAATCTCCATCTCTTGGGTTCGAGCAATTCTCCTGCCTCAGCCTCCCAGGTAGT A G FCHO1 Ensembl:ENSG00000130475 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1334559111 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81082,RMVar_hsa_circ_193376,RMVar_hsa_circ_122521,RMVar_hsa_circ_100852,RMVar_hsa_circ_193380,RMVar_hsa_circ_193382,RMVar_hsa_circ_41081 2393 RMVar_ID_2393 Human_SNP_ID_660276339 A-to-I Human chr19 + 17768194 17768194 17768194 GGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCAGGTAGTTGGGATTACAGGTGTGCTGGTGCACG GGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCGGGTAGTTGGGATTACAGGTGTGCTGGTGCACG A G FCHO1 Ensembl:ENSG00000130475 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1423409197 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81082,RMVar_hsa_circ_193376,RMVar_hsa_circ_122521,RMVar_hsa_circ_100852,RMVar_hsa_circ_193380,RMVar_hsa_circ_193382,RMVar_hsa_circ_41081 2394 RMVar_ID_2394 Human_SNP_ID_660276505 A-to-I Human chr19 + 17768809 17768809 17768809 TATCTGCCTCAGCCTTCCAAAATGTTGGCATTACAGGCATGGGTCACTGTGCCTGGCCAGGAGTG TATCTGCCTCAGCCTTCCAAAATGTTGGCATTTCAGGCATGGGTCACTGTGCCTGGCCAGGAGTG A T FCHO1 Ensembl:ENSG00000130475 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs917360834 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81082,RMVar_hsa_circ_193376,RMVar_hsa_circ_122521,RMVar_hsa_circ_100852,RMVar_hsa_circ_193380,RMVar_hsa_circ_193382,RMVar_hsa_circ_41081 2395 RMVar_ID_2395 Human_SNP_ID_660278987 A-to-I Human chr19 + 17777072 17777072 17777072 TGCCCACCTCGGCTTGCCAAAGTGCTGGGATTACAGGCATGAGCCCTTGTGCCTGGCCCATGCTG TGCCCACCTCGGCTTGCCAAAGTGCTGGGATTGCAGGCATGAGCCCTTGTGCCTGGCCCATGCTG A G FCHO1 Ensembl:ENSG00000130475 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs993317203 Functional Loss SNV dbSNP153 33..33 33 - - - 2396 RMVar_ID_2396 Human_SNP_ID_660279052 A-to-I Human chr19 + 17777397 17777397 17777397 CATCTCTACTAAAAATACAGCATTAGCCAGGCATGGTGGCACATGCCTGTAATCCCAGCTATTCG CATCTCTACTAAAAATACAGCATTAGCCAGGCGTGGTGGCACATGCCTGTAATCCCAGCTATTCG A G FCHO1 Ensembl:ENSG00000130475 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1365225625 Functional Loss SNV dbSNP153 33..33 33 - - - 2397 RMVar_ID_2397 Human_SNP_ID_660293165 A-to-I Human chr19 - 17827717 17827717 17827717 TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTAGTTAAGATGGGGTTTCTCCATGTTGGTCAGGG TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTGTTAAGATGGGGTTTCTCCATGTTGGTCAGGG T A JAK3 Ensembl:ENSG00000105639 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs571551461 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85677,RMVar_hsa_circ_266365,RMVar_hsa_circ_122321,RMVar_hsa_circ_193390,RMVar_hsa_circ_193391 2398 RMVar_ID_2398 Human_SNP_ID_660305549 A-to-I Human chr19 + 17868344 17868344 17868344 CAAACAAAATTGTAGAGTTGGGGTCTCACTATATTGTTCAGGCTGGTCTCCAACTCCTAGCCTCC CAAACAAAATTGTAGAGTTGGGGTCTCACTATGTTGTTCAGGCTGGTCTCCAACTCCTAGCCTCC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1321549033 Functional Loss SNV dbSNP153 33..33 33 - - - 2399 RMVar_ID_2399 Human_SNP_ID_660323981 A-to-I Human chr19 + 17934062 17934062 17934062 AACAGCAGAAATTGCCAGGCACTGTGGCTCACACCTGTAATCCAGGCACTTTGAGAGGCCGAGGC AACAGCAGAAATTGCCAGGCACTGTGGCTCACTCCTGTAATCCAGGCACTTTGAGAGGCCGAGGC A T CCDC124 Ensembl:ENSG00000007080 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs925263436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13392976 RMVar_hsa_circ_193405,RMVar_hsa_circ_116213 2400 RMVar_ID_2400 Human_SNP_ID_660324002 A-to-I Human chr19 + 17934142 17934142 17934142 GGTCAAGAGTTTGAGACCAGCCTGGCCAACATAGTGAAACCCCGTCTCTACTAAAAATACAAAAA GGTCAAGAGTTTGAGACCAGCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAA A G CCDC124 Ensembl:ENSG00000007080 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1273288382 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2710185 RMVar_hsa_circ_193405,RMVar_hsa_circ_116213 2401 RMVar_ID_2401 Human_SNP_ID_660324082 A-to-I Human chr19 + 17934367 17934367 17934367 GAGATTGTGCCACTGCATTCCAGCCTGGGTGAAAGAGCAAAACTCCGTCTCAAAACAAAAAAAAG GAGATTGTGCCACTGCATTCCAGCCTGGGTGACAGAGCAAAACTCCGTCTCAAAACAAAAAAAAG A C CCDC124 Ensembl:ENSG00000007080 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1275930286 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193405,RMVar_hsa_circ_116213 2402 RMVar_ID_2402 Human_SNP_ID_660324144 A-to-I Human chr19 + 17934604 17934604 17934604 GCCCAGGAGTTCAAGGCCAGCCTGGGCAACATAGTCAGACCCTGCCTTAAAAAAAAAAAAAAAAA GCCCAGGAGTTCAAGGCCAGCCTGGGCAACATGGTCAGACCCTGCCTTAAAAAAAAAAAAAAAAA A G CCDC124 Ensembl:ENSG00000007080 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1054118250 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193405,RMVar_hsa_circ_116213 2403 RMVar_ID_2403 Human_SNP_ID_660324184 A-to-I Human chr19 + 17934727 17934727 17934727 ATCACTTGAGCCCAGGAGGTCAAGGCTGCAGTAAGCCGAGATTTCGCCACTGCACTCCAGCCTGG ATCACTTGAGCCCAGGAGGTCAAGGCTGCAGTGAGCCGAGATTTCGCCACTGCACTCCAGCCTGG A G CCDC124 Ensembl:ENSG00000007080 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1418127685 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193405,RMVar_hsa_circ_116213 2404 RMVar_ID_2404 Human_SNP_ID_660324258 A-to-I Human chr19 + 17934932 17934931 17934932 GTTTCCTTGTTTCCTTTTTTTTTTTTTCTTTTAAGAGACAGGGTCTTGTTCTGTTGCCCAGGCTG GTTTCCTTGTTTCCTTTTTTTTTTTTTCTTTT_AGAGACAGGGTCTTGTTCTGTTGCCCAGGCTG TA T CCDC124 Ensembl:ENSG00000007080 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1242985331 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_2559052 RMVar_hsa_circ_193405,RMVar_hsa_circ_116213 2405 RMVar_ID_2405 Human_SNP_ID_660324259 A-to-I Human chr19 + 17934932 17934932 17934932 GTTTCCTTGTTTCCTTTTTTTTTTTTTCTTTTAAGAGACAGGGTCTTGTTCTGTTGCCCAGGCTG GTTTCCTTGTTTCCTTTTTTTTTTTTTCTTTTTAGAGACAGGGTCTTGTTCTGTTGCCCAGGCTG A T CCDC124 Ensembl:ENSG00000007080 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1475211315 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2559052 RMVar_hsa_circ_193405,RMVar_hsa_circ_116213 2406 RMVar_ID_2406 Human_SNP_ID_660324277 A-to-I Human chr19 + 17935015 17935015 17935015 ATAGCTCACTGTGGCCTCAGCCTCCTACGCTCAGGCGATCCTTCCACCTCAGCCTCCTAAGTAGC ATAGCTCACTGTGGCCTCAGCCTCCTACGCTCGGGCGATCCTTCCACCTCAGCCTCCTAAGTAGC A G CCDC124 Ensembl:ENSG00000007080 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1045456576 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193405,RMVar_hsa_circ_116213 2407 RMVar_ID_2407 Human_SNP_ID_660324284 A-to-I Human chr19 + 17935041 17935041 17935041 ACGCTCAGGCGATCCTTCCACCTCAGCCTCCTAAGTAGCTGGAACTACAGGCACAAGCCACTGTG ACGCTCAGGCGATCCTTCCACCTCAGCCTCCTCAGTAGCTGGAACTACAGGCACAAGCCACTGTG A C CCDC124 Ensembl:ENSG00000007080 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1001263430 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193405,RMVar_hsa_circ_116213 2408 RMVar_ID_2408 Human_SNP_ID_660324296 A-to-I Human chr19 + 17935112 17935112 17935112 TATTTTTTATTTTGTAGAGACGGACTCTTGCTATGTTGCCCAGGCTGGTCTTGAACTCCTGGCCT TATTTTTTATTTTGTAGAGACGGACTCTTGCTGTGTTGCCCAGGCTGGTCTTGAACTCCTGGCCT A G CCDC124 Ensembl:ENSG00000007080 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1280550678 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13392980 Human_Splice_Rec_1978965 RMVar_hsa_circ_101232,RMVar_hsa_circ_193405,RMVar_hsa_circ_116213,RMVar_hsa_circ_110766,RMVar_hsa_circ_193407,RMVar_hsa_circ_78872,RMVar_hsa_circ_193408,RMVar_hsa_circ_193406 2409 RMVar_ID_2409 Human_SNP_ID_660324443 A-to-I Human chr19 + 17935613 17935609 17935613 CAGCTTTTTGGTTTTTTTTGAGAGTGAGTCTCACTCTGCCGCCTAGGCTGGAGTGCAGTTGCACG CAGCTTTTTGGTTTTTTTTGAGAGTGAGT____CTCTGCCGCCTAGGCTGGAGTGCAGTTGCACG TCTCA T CCDC124 Ensembl:ENSG00000007080 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1418104433 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_515939,Human_RBP_ID_23786390 RMVar_hsa_circ_101232,RMVar_hsa_circ_193405,RMVar_hsa_circ_116213,RMVar_hsa_circ_110766,RMVar_hsa_circ_193407,RMVar_hsa_circ_78872,RMVar_hsa_circ_193408,RMVar_hsa_circ_193406 2410 RMVar_ID_2410 Human_SNP_ID_660324444 A-to-I Human chr19 + 17935613 17935613 17935613 CAGCTTTTTGGTTTTTTTTGAGAGTGAGTCTCACTCTGCCGCCTAGGCTGGAGTGCAGTTGCACG CAGCTTTTTGGTTTTTTTTGAGAGTGAGTCTCGCTCTGCCGCCTAGGCTGGAGTGCAGTTGCACG A G CCDC124 Ensembl:ENSG00000007080 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1191930219 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_515939,Human_RBP_ID_23786390 RMVar_hsa_circ_101232,RMVar_hsa_circ_193405,RMVar_hsa_circ_116213,RMVar_hsa_circ_110766,RMVar_hsa_circ_193407,RMVar_hsa_circ_78872,RMVar_hsa_circ_193408,RMVar_hsa_circ_193406 2411 RMVar_ID_2411 Human_SNP_ID_660324472 A-to-I Human chr19 + 17935699 17935699 17935699 TGCCTCCCAGGTTCAAGCGGCTTTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTAAAGGTGTCCG TGCCTCCCAGGTTCAAGCGGCTTTCCTGCCTCGGCCTCCTGAGTAGCTGGGATTAAAGGTGTCCG A G CCDC124 Ensembl:ENSG00000007080 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs545504451 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2771323 RMVar_hsa_circ_101232,RMVar_hsa_circ_193405,RMVar_hsa_circ_116213,RMVar_hsa_circ_110766,RMVar_hsa_circ_193407,RMVar_hsa_circ_78872,RMVar_hsa_circ_193408,RMVar_hsa_circ_193406 2412 RMVar_ID_2412 Human_SNP_ID_660324495 A-to-I Human chr19 + 17935817 17935817 17935817 GTTGACTAGACTGGTTTTGAACTCCTGACCTCAGGTGATCCGCCCACCTTGGCCTCCCAAAGTGC GTTGACTAGACTGGTTTTGAACTCCTGACCTCCGGTGATCCGCCCACCTTGGCCTCCCAAAGTGC A C CCDC124 Ensembl:ENSG00000007080 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1433559357 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2697949,Human_miRNA_ID_2874192,Human_miRNA_ID_2982153 RMVar_hsa_circ_101232,RMVar_hsa_circ_193405,RMVar_hsa_circ_116213,RMVar_hsa_circ_110766,RMVar_hsa_circ_193407,RMVar_hsa_circ_78872,RMVar_hsa_circ_193408,RMVar_hsa_circ_193406 2413 RMVar_ID_2413 Human_SNP_ID_660324503 A-to-I Human chr19 + 17935851 17935851 17935851 GTGATCCGCCCACCTTGGCCTCCCAAAGTGCTAGGATTACAGGCGTGAGCCACTGTGCCTGGCCG GTGATCCGCCCACCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGTGCCTGGCCG A G CCDC124 Ensembl:ENSG00000007080 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1461051978 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2229375 RMVar_hsa_circ_101232,RMVar_hsa_circ_193405,RMVar_hsa_circ_116213,RMVar_hsa_circ_110766,RMVar_hsa_circ_193407,RMVar_hsa_circ_78872,RMVar_hsa_circ_193408,RMVar_hsa_circ_193406 2414 RMVar_ID_2414 Human_SNP_ID_660324541 A-to-I Human chr19 + 17935966 17935966 17935966 TCACTCTGTCGCCCAGGCTGGAGTGCAGTGGCACGATCTTGGCTCACTTCAACCTCCACCTCCCG TCACTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCGATCTTGGCTCACTTCAACCTCCACCTCCCG A G CCDC124 Ensembl:ENSG00000007080 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1291477277 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101232,RMVar_hsa_circ_193405,RMVar_hsa_circ_116213,RMVar_hsa_circ_110766,RMVar_hsa_circ_193407,RMVar_hsa_circ_78872,RMVar_hsa_circ_193408,RMVar_hsa_circ_193406 2415 RMVar_ID_2415 Human_SNP_ID_660324581 A-to-I Human chr19 + 17936119 17936119 17936119 TGGAGATGGGGTTTTGCCGTGTTGGCCAGGCTAGTCTCGAACTTCTGACCGCAAGTGATCCGCCC TGGAGATGGGGTTTTGCCGTGTTGGCCAGGCTGGTCTCGAACTTCTGACCGCAAGTGATCCGCCC A G CCDC124 Ensembl:ENSG00000007080 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1392556511 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101232,RMVar_hsa_circ_193405,RMVar_hsa_circ_116213,RMVar_hsa_circ_110766,RMVar_hsa_circ_193407,RMVar_hsa_circ_78872,RMVar_hsa_circ_193408,RMVar_hsa_circ_193406 2416 RMVar_ID_2416 Human_SNP_ID_660325144 A-to-I Human chr19 + 17938130 17938130 17938130 GGGAGGCTGAGGTGAGAGGATTGCTTGAGGCCAGGAGCTCCAGGCCAGCCTGGGCAACATAGCAA GGGAGGCTGAGGTGAGAGGATTGCTTGAGGCCGGGAGCTCCAGGCCAGCCTGGGCAACATAGCAA A G CCDC124 Ensembl:ENSG00000007080 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1180143934 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55946,RMVar_hsa_circ_101232,RMVar_hsa_circ_193407,RMVar_hsa_circ_78872,RMVar_hsa_circ_193408 2417 RMVar_ID_2417 Human_SNP_ID_660343429 A-to-I Human chr19 + 18003290 18003290 18003290 TCCGTTTTTGTGTTTGTTTTTGTTTTTGAGACAGGGTCTTACTCTGTTACTCAGGCTGGAGTGCA TCCGTTTTTGTGTTTGTTTTTGTTTTTGAGACGGGGTCTTACTCTGTTACTCAGGCTGGAGTGCA A G ARRDC2 Ensembl:ENSG00000105643 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1282273264 Functional Loss SNV dbSNP153 33..33 33 - - - 2418 RMVar_ID_2418 Human_SNP_ID_660343720 A-to-I Human chr19 + 18004109 18004109 18004109 TCTCTTTAAATACATAAAAATTGGCTGGGCGCAGTGGCTTATGCCTGTAATCCCAGTACTTTGGG TCTCTTTAAATACATAAAAATTGGCTGGGCGCGGTGGCTTATGCCTGTAATCCCAGTACTTTGGG A G ARRDC2 Ensembl:ENSG00000105643 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965406132 Functional Loss SNV dbSNP153 33..33 33 - - - 2419 RMVar_ID_2419 Human_SNP_ID_660343921 A-to-I Human chr19 + 18004853 18004853 18004853 GAAACCCCATCTTTACAAAAAATACAAAAATTAGCGGGGCATGGTGGTACACACCTGTAATCCCG GAAACCCCATCTTTACAAAAAATACAAAAATTGGCGGGGCATGGTGGTACACACCTGTAATCCCG A G ARRDC2 Ensembl:ENSG00000105643 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1395833790 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13393125 2420 RMVar_ID_2420 Human_SNP_ID_660351880 A-to-I Human chr19 + 18030699 18030699 18030699 CAAGAATGCATCTTGTCTTGTTCTTGCAGCCCAGCATGCCAGTGCTTCCTCCATGAATTTGAAAG CAAGAATGCATCTTGTCTTGTTCTTGCAGCCCGGCATGCCAGTGCTTCCTCCATGAATTTGAAAG A G AC020904.2 Ensembl:ENSG00000273654 Pseudogene exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1241667450 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1979078 Human_miRNA_ID_1868488,Human_miRNA_ID_1909089 2421 RMVar_ID_2421 Human_SNP_ID_660362912 A-to-I Human chr19 - 18071260 18071259 18071260 TCAAGAGATTCTCCTGCTTCAGCCTCCCGAGTAGCTGGGATTACAGGCATCTGCCACCATACCCG TCAAGAGATTCTCCTGCTTCAGCCTCCCGAGT_GCTGGGATTACAGGCATCTGCCACCATACCCG CT C IL12RB1 Ensembl:ENSG00000096996 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1456100658 Functional Loss DEL dbSNP153 33..33 33 - - - Human_Splice_Rec_1979162 RMVar_hsa_circ_193415,RMVar_hsa_circ_83500 2422 RMVar_ID_2422 Human_SNP_ID_660362938 A-to-I Human chr19 - 18071320 18071320 18071320 CTTTTTTTTCTTGTGACAGATGGCATGATCTCAGCTCACTGCAACCTCCGCCTTCCAGATTCAAG CTTTTTTTTCTTGTGACAGATGGCATGATCTCGGCTCACTGCAACCTCCGCCTTCCAGATTCAAG T C IL12RB1 Ensembl:ENSG00000096996 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1285632810 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1979162 RMVar_hsa_circ_193415,RMVar_hsa_circ_83500 2423 RMVar_ID_2423 Human_SNP_ID_660370894 A-to-I Human chr19 + 18100360 18100360 18100360 GTTGGCCAGGCTGGTATCAAACTCCTGATCTCAGGTGATCCGCCCACCTCGGCCTCCCAAAGTGC GTTGGCCAGGCTGGTATCAAACTCCTGATCTCGGGTGATCCGCCCACCTCGGCCTCCCAAAGTGC A G MAST3 Ensembl:ENSG00000099308 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1568541553 Functional Loss SNV dbSNP153 33..33 33 - - - 2424 RMVar_ID_2424 Human_SNP_ID_660377613 A-to-I Human chr19 + 18125698 18125698 18125698 TGGAGGCGGAGGTTGCAGTGAGCCGAGATCACACCACTTCATTCCAGCCTGGGCAACAGGGCAAG TGGAGGCGGAGGTTGCAGTGAGCCGAGATCACGCCACTTCATTCCAGCCTGGGCAACAGGGCAAG A G MAST3 Ensembl:ENSG00000099308 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs555131564 Functional Loss SNV dbSNP153 33..33 33 - - - 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_83812,RMVar_hsa_circ_193429,RMVar_hsa_circ_78180,RMVar_hsa_circ_193428,RMVar_hsa_circ_193426,RMVar_hsa_circ_52932,RMVar_hsa_circ_111759,RMVar_hsa_circ_193430 2425 RMVar_ID_2425 Human_SNP_ID_660377811 A-to-I Human chr19 + 18126510 18126510 18126510 GAAAGCTGGGGAGGCCCGGCATGGTAGCTCACACTTGTAATCCCAGCACTGTGGGAGGCCAAGGC GAAAGCTGGGGAGGCCCGGCATGGTAGCTCACCCTTGTAATCCCAGCACTGTGGGAGGCCAAGGC A C MAST3 Ensembl:ENSG00000099308 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1388462963 Functional Loss SNV dbSNP153 33..33 33 - - - 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_83812,RMVar_hsa_circ_193429,RMVar_hsa_circ_78180,RMVar_hsa_circ_193428,RMVar_hsa_circ_193426,RMVar_hsa_circ_52932,RMVar_hsa_circ_111759,RMVar_hsa_circ_193430 2426 RMVar_ID_2426 Human_SNP_ID_660382484 A-to-I Human chr19 + 18143304 18143304 18143304 GGGTTTTAAAAGTTGAATAGGAAGCCGGGTGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGG GGGTTTTAAAAGTTGAATAGGAAGCCGGGTGCCGTGGCTCACGCCTGTAATCCCAGCACTTTGGG A C MAST3 Ensembl:ENSG00000099308 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1001990314 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44924,RMVar_hsa_circ_112186,RMVar_hsa_circ_193429,RMVar_hsa_circ_78180,RMVar_hsa_circ_193428,RMVar_hsa_circ_52932,RMVar_hsa_circ_51567,RMVar_hsa_circ_68816,RMVar_hsa_circ_48676 2427 RMVar_ID_2427 Human_SNP_ID_660391858 A-to-I Human chr19 + 18173937 18173937 18173937 GCGGCGGTGCAGGCGTCCCCTCTGCAAGCGTTAGACTTCTTTGGGAATGGGCCACCAGTTAACTA GCGGCGGTGCAGGCGTCCCCTCTGCAAGCGTTGGACTTCTTTGGGAATGGGCCACCAGTTAACTA A G IFI30,AC007192.1 Ensembl:ENSG00000216490,Ensembl:ENSG00000268173 Protein coding,Protein coding CDS,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs11554160 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_54731,Human_RBP_ID_4509999,Human_RBP_ID_22447558,Human_RBP_ID_22763953 Human_Splice_Rec_1979317,Human_Splice_Rec_1979465,Human_Splice_Rec_1979467 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_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_193451 2428 RMVar_ID_2428 Human_SNP_ID_660395290 A-to-I Human chr19 + 18186011 18186011 18186011 CTCCTGTCTCAGCCTCCCAAGTAGTTGGGACTAGAGTTGCACACCACCACACCTGGCTAATTTTT CTCCTGTCTCAGCCTCCCAAGTAGTTGGGACTGGAGTTGCACACCACCACACCTGGCTAATTTTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1300920605 Functional Loss SNV dbSNP153 33..33 33 - - - 2429 RMVar_ID_2429 Human_SNP_ID_660419630 A-to-I Human chr19 - 18270691 18270691 18270691 CCGAGATTGTGACGCTGCACTCCAGCCTGGGCAAAAGGGTGGGACTCTGTTTTAAAAACAAAAAA CCGAGATTGTGACGCTGCACTCCAGCCTGGGCGAAAGGGTGGGACTCTGTTTTAAAAACAAAAAA T C IQCN Ensembl:ENSG00000130518 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1488592623 Functional Loss SNV dbSNP153 33..33 33 - - - 2430 RMVar_ID_2430 Human_SNP_ID_660422202 A-to-I Human chr19 - 18278609 18278609 18278609 AGGCTCACTGCAACCTCTGCCTCCCCGGGCTCAAGTGATTCTCCTGCCTCAGCCTCCAAGTAGCT AGGCTCACTGCAACCTCTGCCTCCCCGGGCTCGAGTGATTCTCCTGCCTCAGCCTCCAAGTAGCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459738047 Functional Loss SNV dbSNP153 33..33 33 - - - 2431 RMVar_ID_2431 Human_SNP_ID_660426129 A-to-I Human chr19 - 18289872 18289872 18289872 AGCATGGTCGTCGGGCGCAGTGGCTCATGCCTATAATCCCAGAACTTTTGGAGGTTGAGGCAGGC AGCATGGTCGTCGGGCGCAGTGGCTCATGCCTGTAATCCCAGAACTTTTGGAGGTTGAGGCAGGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1391965244 Functional Loss SNV dbSNP153 33..33 33 - - - 2432 RMVar_ID_2432 Human_SNP_ID_660433042 A-to-I Human chr19 - 18313107 18313106 18313108 TCAAACAGTTCTCCTGCCTCAGGCTCCCGAGTAGCTGGGACTACAGGCATGCACCACCATGCCCA TCAAACAGTTCTCCTGCCTCAGGCTCCCGAG__GCTGGGACTACAGGCATGCACCACCATGCCCA CTA C LSM4 Ensembl:ENSG00000130520 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs776678645 Functional Loss DEL dbSNP153 32..33 33 - - - 2433 RMVar_ID_2433 Human_SNP_ID_660433196 A-to-I Human chr19 + 18313790 18313790 18313790 CTCCTGTCTTGGCCTCCCGGGGTGCTGGGATTATAGGCATTAGCCACCACACTCAGTCCAAGCCT CTCCTGTCTTGGCCTCCCGGGGTGCTGGGATTGTAGGCATTAGCCACCACACTCAGTCCAAGCCT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs368160379 Functional Loss SNV dbSNP153 33..33 33 - - - 2434 RMVar_ID_2434 Human_SNP_ID_660433610 A-to-I Human chr19 + 18315350 18315350 18315350 TTTTATATTTTATGGAGAGACGTGGTTTCTCCATGTTGCCTAGACTGGTCTCTGAACTCCTGGGC TTTTATATTTTATGGAGAGACGTGGTTTCTCCCTGTTGCCTAGACTGGTCTCTGAACTCCTGGGC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1015630552 Functional Loss SNV dbSNP153 33..33 33 - - - 2435 RMVar_ID_2435 Human_SNP_ID_660433611 A-to-I Human chr19 + 18315350 18315350 18315350 TTTTATATTTTATGGAGAGACGTGGTTTCTCCATGTTGCCTAGACTGGTCTCTGAACTCCTGGGC TTTTATATTTTATGGAGAGACGTGGTTTCTCCGTGTTGCCTAGACTGGTCTCTGAACTCCTGGGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1015630552 Functional Loss SNV dbSNP153 33..33 33 - - - 2436 RMVar_ID_2436 Human_SNP_ID_660433626 A-to-I Human chr19 + 18315403 18315403 18315403 GAACTCCTGGGCTGAAGCCATCCTCTAGCCTCAGCCTCCCAAAGTGCTGGAATTATAGGCCTGAG GAACTCCTGGGCTGAAGCCATCCTCTAGCCTCGGCCTCCCAAAGTGCTGGAATTATAGGCCTGAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs888565655 Functional Loss SNV dbSNP153 33..33 33 - - - 2437 RMVar_ID_2437 Human_SNP_ID_660434068 A-to-I Human chr19 - 18317032 18317032 18317032 TGGGTGACAGGCTTGCTTCCCAGGCTCAAGCAATCCTCCTGCCTCAGCACCCAAGTAGCTGGGAC TGGGTGACAGGCTTGCTTCCCAGGCTCAAGCAGTCCTCCTGCCTCAGCACCCAAGTAGCTGGGAC T C LSM4 Ensembl:ENSG00000130520 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1163367626 Functional Loss SNV dbSNP153 33..33 33 - - - 2438 RMVar_ID_2438 Human_SNP_ID_660434283 A-to-I Human chr19 + 18317733 18317733 18317733 TTTTTTTTTTGATGGTGACAGGCTTTTACTATATTGCCCAAGCTGGTTTTGAACTCTTGGCCTCA TTTTTTTTTTGATGGTGACAGGCTTTTACTATGTTGCCCAAGCTGGTTTTGAACTCTTGGCCTCA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1443448084 Functional Loss SNV dbSNP153 33..33 33 - - - 2439 RMVar_ID_2439 Human_SNP_ID_660443352 A-to-I Human chr19 + 18352324 18352301 18352325 TTGGGTGTTTTCCCAGTACTCGGGAGTACTGTAATCCCAGTACTCGGGAGGATGAGGCAGAAGGA TTGGGTGTTT________________________TCCCAGTACTCGGGAGGATGAGGCAGAAGGA TTCCCAGTACTCGGGAGTACTGTAA T PGPEP1 Ensembl:ENSG00000130517 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs371373225 Functional Loss DEL dbSNP153 11..34 33 - - - RMVar_hsa_circ_108567,RMVar_hsa_circ_193465,RMVar_hsa_circ_193466,RMVar_hsa_circ_110890 2440 RMVar_ID_2440 Human_SNP_ID_660443361 A-to-I Human chr19 + 18352324 18352324 18352324 TTGGGTGTTTTCCCAGTACTCGGGAGTACTGTAATCCCAGTACTCGGGAGGATGAGGCAGAAGGA TTGGGTGTTTTCCCAGTACTCGGGAGTACTGTTATCCCAGTACTCGGGAGGATGAGGCAGAAGGA A T PGPEP1 Ensembl:ENSG00000130517 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs746841281 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108567,RMVar_hsa_circ_193465,RMVar_hsa_circ_193466,RMVar_hsa_circ_110890 2441 RMVar_ID_2441 Human_SNP_ID_660443369 A-to-I Human chr19 + 18352350 18352350 18352350 TACTGTAATCCCAGTACTCGGGAGGATGAGGCAGAAGGAACTCTTGAGGCCGGGAAGCAGAGGTT TACTGTAATCCCAGTACTCGGGAGGATGAGGCCGAAGGAACTCTTGAGGCCGGGAAGCAGAGGTT A C PGPEP1 Ensembl:ENSG00000130517 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1490353733 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108567,RMVar_hsa_circ_193465,RMVar_hsa_circ_193466,RMVar_hsa_circ_110890 2442 RMVar_ID_2442 Human_SNP_ID_660445144 A-to-I Human chr19 + 18359030 18359030 18359030 TAAATCAGGGCCAGGCGCAGTGGCTCATGCCTATAATCCTAGCACTTCGGGAGGCCAAGGCAGGA TAAATCAGGGCCAGGCGCAGTGGCTCATGCCTGTAATCCTAGCACTTCGGGAGGCCAAGGCAGGA A G PGPEP1 Ensembl:ENSG00000130517 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs555409702 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108567,RMVar_hsa_circ_193465 2443 RMVar_ID_2443 Human_SNP_ID_660445943 A-to-I Human chr19 + 18362516 18362516 18362516 GGGAGGCTGAGGTAGGCGGATCACTACAGGTCAGGAGTTTCAGAACAGCCTGGCCAGCATGGTGA GGGAGGCTGAGGTAGGCGGATCACTACAGGTCGGGAGTTTCAGAACAGCCTGGCCAGCATGGTGA A G PGPEP1 Ensembl:ENSG00000130517 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs913379712 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108567,RMVar_hsa_circ_193465 2444 RMVar_ID_2444 Human_SNP_ID_660446824 A-to-I Human chr19 + 18364493 18364493 18364493 AAAATTAGCCGGGCATGGTGATGAGTGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCTGGAGA AAAATTAGCCGGGCATGGTGATGAGTGCCTGTGGTCCCAGCTACTCGGGAGGCTGAGGCTGGAGA A G PGPEP1 Ensembl:ENSG00000130517 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1471953859 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1093751 RMVar_hsa_circ_108567,RMVar_hsa_circ_193465 2445 RMVar_ID_2445 Human_SNP_ID_660446837 A-to-I Human chr19 + 18364546 18364546 18364546 TGAGGCTGGAGAATCGCTTGAACTTGGGAGGCAGAGGTTGCAGTGAGCTGAGATTGCACAGCTGC TGAGGCTGGAGAATCGCTTGAACTTGGGAGGCGGAGGTTGCAGTGAGCTGAGATTGCACAGCTGC A G PGPEP1 Ensembl:ENSG00000130517 Protein coding 3'UTR GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line - 24183664,31158229 RNA-Seq:(High) rs896416951 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108567,RMVar_hsa_circ_193465 2446 RMVar_ID_2446 Human_SNP_ID_660447083 A-to-I Human chr19 + 18365401 18365401 18365401 GTCTTGTTCTGTTGACCAGGCTGGAGTACAGTAGTGTGATCATGGATCACTGCAGCCTCTACCTC GTCTTGTTCTGTTGACCAGGCTGGAGTACAGTGGTGTGATCATGGATCACTGCAGCCTCTACCTC A G PGPEP1 Ensembl:ENSG00000130517 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs567573185 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26472235 RMVar_hsa_circ_108567,RMVar_hsa_circ_193465 2447 RMVar_ID_2447 Human_SNP_ID_660447096 A-to-I Human chr19 + 18365442 18365442 18365442 ATGGATCACTGCAGCCTCTACCTCCTGGGCTCAAGTGATCCTCCCATCTCAGCCTCCTGAGTAGC ATGGATCACTGCAGCCTCTACCTCCTGGGCTCTAGTGATCCTCCCATCTCAGCCTCCTGAGTAGC A T PGPEP1 Ensembl:ENSG00000130517 Protein coding 3'UTR GSE38233;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,32596459 RNA-Seq:(High) rs1359271996 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108567,RMVar_hsa_circ_193465 2448 RMVar_ID_2448 Human_SNP_ID_660447103 A-to-I Human chr19 + 18365455 18365455 18365455 GCCTCTACCTCCTGGGCTCAAGTGATCCTCCCATCTCAGCCTCCTGAGTAGCTGGGACTACAGGC GCCTCTACCTCCTGGGCTCAAGTGATCCTCCCGTCTCAGCCTCCTGAGTAGCTGGGACTACAGGC A G PGPEP1 Ensembl:ENSG00000130517 Protein coding 3'UTR GSE38233;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,32596459 RNA-Seq:(High) rs1390386724 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108567,RMVar_hsa_circ_193465 2449 RMVar_ID_2449 Human_SNP_ID_660447111 A-to-I Human chr19 + 18365515 18365515 18365515 CAGGCATGCACCACCACACCTGGCTAATTTTTAAATTTTTTATACAGACAGGGTTTCACCATGTT CAGGCATGCACCACCACACCTGGCTAATTTTTGAATTTTTTATACAGACAGGGTTTCACCATGTT A G PGPEP1 Ensembl:ENSG00000130517 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1024413257 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108567,RMVar_hsa_circ_193465 2450 RMVar_ID_2450 Human_SNP_ID_660447115 A-to-I Human chr19 + 18365543 18365543 18365543 TTTTAAATTTTTTATACAGACAGGGTTTCACCATGTTGCCCAGGCTGGTCTCGAACTCCTGGACT TTTTAAATTTTTTATACAGACAGGGTTTCACCGTGTTGCCCAGGCTGGTCTCGAACTCCTGGACT A G PGPEP1 Ensembl:ENSG00000130517 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs769271236 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108567,RMVar_hsa_circ_193465 2451 RMVar_ID_2451 Human_SNP_ID_660447333 A-to-I Human chr19 + 18366519 18366519 18366519 TTGAGATGGATTCTCACACTGTTACTCGGGCTAGAGTGCAATGGCGTGATCTCGGCTCACTGCAA TTGAGATGGATTCTCACACTGTTACTCGGGCTGGAGTGCAATGGCGTGATCTCGGCTCACTGCAA A G PGPEP1 Ensembl:ENSG00000130517 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs1003597069 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26466011 RMVar_hsa_circ_108567,RMVar_hsa_circ_193465 2452 RMVar_ID_2452 Human_SNP_ID_660447343 A-to-I Human chr19 + 18366550 18366550 18366550 TAGAGTGCAATGGCGTGATCTCGGCTCACTGCAACCTCCACCTCCTGGGTTTACACAATTCTCCT TAGAGTGCAATGGCGTGATCTCGGCTCACTGCGACCTCCACCTCCTGGGTTTACACAATTCTCCT A G PGPEP1 Ensembl:ENSG00000130517 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs529858421 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108567,RMVar_hsa_circ_193465 2453 RMVar_ID_2453 Human_SNP_ID_660447446 A-to-I Human chr19 + 18367105 18367105 18367105 CTATGCCTGGGAGGTTGAAGCCCCAGTGAGCCATGATCACACCACTGTAGTCCAGCCCGGGTGAC CTATGCCTGGGAGGTTGAAGCCCCAGTGAGCCGTGATCACACCACTGTAGTCCAGCCCGGGTGAC A G PGPEP1 Ensembl:ENSG00000130517 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs898863716 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108567,RMVar_hsa_circ_193465 2454 RMVar_ID_2454 Human_SNP_ID_660447752 A-to-I Human chr19 + 18368183 18368183 18368183 AGGGGGGCCAGGCGCAGTGGCTTATGCCTGTTATCCCAGCACTTTGGGAGGCCAAGGCAGACTGA AGGGGGGCCAGGCGCAGTGGCTTATGCCTGTTGTCCCAGCACTTTGGGAGGCCAAGGCAGACTGA A G PGPEP1 Ensembl:ENSG00000130517 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1460999767 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108567,RMVar_hsa_circ_193465 2455 RMVar_ID_2455 Human_SNP_ID_660447774 A-to-I Human chr19 + 18368291 18368291 18368291 AAAACCCCATCTCTACTAAAAATACAAAAATTAGTCAAGAGTGGATGGTGCGTGCCTGTAATCCC AAAACCCCATCTCTACTAAAAATACAAAAATTGGTCAAGAGTGGATGGTGCGTGCCTGTAATCCC A G PGPEP1 Ensembl:ENSG00000130517 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1307310752 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1093754,Human_RBP_ID_23786589 RMVar_hsa_circ_108567,RMVar_hsa_circ_193465 2456 RMVar_ID_2456 Human_SNP_ID_660447787 A-to-I Human chr19 + 18368345 18368345 18368345 CCTGTAATCCCAGCTACCTGGGAGGCTGAGACAGGAGAATTGCTTGAACCTGGGAGGCAGAGGTT CCTGTAATCCCAGCTACCTGGGAGGCTGAGACGGGAGAATTGCTTGAACCTGGGAGGCAGAGGTT A G PGPEP1 Ensembl:ENSG00000130517 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs919054370 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22591452 RMVar_hsa_circ_108567,RMVar_hsa_circ_193465 2457 RMVar_ID_2457 Human_SNP_ID_660496295 A-to-I Human chr19 - 18534644 18534644 18534644 CTAGGAGTTTGAGGCTGCAGTGAGCTATGATCATGCCATTGCACTCCAGCCTGGGTGACCGATCA CTAGGAGTTTGAGGCTGCAGTGAGCTATGATCGTGCCATTGCACTCCAGCCTGGGTGACCGATCA T C FKBP8 Ensembl:ENSG00000105701 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs778637134 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13395219,Human_RBP_ID_25389235 RMVar_hsa_circ_45679,RMVar_hsa_circ_114996,RMVar_hsa_circ_267425,RMVar_hsa_circ_193481 2458 RMVar_ID_2458 Human_SNP_ID_660496330 A-to-I Human chr19 - 18534733 18534733 18534733 AATACATAAATAAATAATTCGTTGGACATGGTAGTACACGCCTGTAGTCCCAGCTCCTCGGGAGG AATACATAAATAAATAATTCGTTGGACATGGTCGTACACGCCTGTAGTCCCAGCTCCTCGGGAGG T G FKBP8 Ensembl:ENSG00000105701 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1162544078 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45679,RMVar_hsa_circ_114996,RMVar_hsa_circ_267425,RMVar_hsa_circ_193481 2459 RMVar_ID_2459 Human_SNP_ID_660503938 A-to-I Human chr19 + 18560130 18560130 18560130 AGGTTCAAGCCATTCTCCTGCCTCAGCCATCCAAGTAGCTGCGACTACAGGTGCCCGCCACCATG AGGTTCAAGCCATTCTCCTGCCTCAGCCATCCGAGTAGCTGCGACTACAGGTGCCCGCCACCATG A G KXD1 Ensembl:ENSG00000105700 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,31158229,32596459 RNA-Seq:(High) rs1292167154 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1980658 2460 RMVar_ID_2460 Human_SNP_ID_660504109 A-to-I Human chr19 + 18560887 18560887 18560887 CACCACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACTATGTTGGCCAGGC CACCACCATGCCTGGCTAATTTTTGTATTTTTGGTAGAGATGGGGTTTCACTATGTTGGCCAGGC A G KXD1 Ensembl:ENSG00000105700 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1393678086 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76805,RMVar_hsa_circ_193493 2461 RMVar_ID_2461 Human_SNP_ID_660504127 A-to-I Human chr19 + 18560973 18560973 18560973 GTGATCCACCTGCCTCGCCCTCCCAGAGTGCTAGGATTACAGGCGTGAGCCACAGCACCTGGCCA GTGATCCACCTGCCTCGCCCTCCCAGAGTGCTGGGATTACAGGCGTGAGCCACAGCACCTGGCCA A G KXD1 Ensembl:ENSG00000105700 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1412254477 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23174925 RMVar_hsa_circ_76805,RMVar_hsa_circ_193493 2462 RMVar_ID_2462 Human_SNP_ID_660504171 A-to-I Human chr19 + 18561139 18561139 18561139 TCAAGGTAAAGGGTGGCTGGGCGCAGTGGCTCAGGCCTGTAATCCTAGCACTTTGGGAGGCCAAG TCAAGGTAAAGGGTGGCTGGGCGCAGTGGCTCGGGCCTGTAATCCTAGCACTTTGGGAGGCCAAG A G KXD1 Ensembl:ENSG00000105700 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1003221247 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76805,RMVar_hsa_circ_193493 2463 RMVar_ID_2463 Human_SNP_ID_660508029 A-to-I Human chr19 + 18574097 18574097 18574097 CACAAGGTCAAGAGATTGAGATCATCATGACCAACATGGTGAAATCCCATCTCTACTAAAAATAC CACAAGGTCAAGAGATTGAGATCATCATGACCTACATGGTGAAATCCCATCTCTACTAAAAATAC A T UBA52 Ensembl:ENSG00000221983 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1453218176 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193498,RMVar_hsa_circ_96992,RMVar_hsa_circ_193500,RMVar_hsa_circ_75863,RMVar_hsa_circ_115874,RMVar_hsa_circ_193499,RMVar_hsa_circ_370443,RMVar_hsa_circ_193504 2464 RMVar_ID_2464 Human_SNP_ID_660508031 A-to-I Human chr19 + 18574100 18574100 18574100 AAGGTCAAGAGATTGAGATCATCATGACCAACATGGTGAAATCCCATCTCTACTAAAAATACAAA AAGGTCAAGAGATTGAGATCATCATGACCAACGTGGTGAAATCCCATCTCTACTAAAAATACAAA A G UBA52 Ensembl:ENSG00000221983 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs898254427 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193498,RMVar_hsa_circ_96992,RMVar_hsa_circ_193500,RMVar_hsa_circ_75863,RMVar_hsa_circ_115874,RMVar_hsa_circ_193499,RMVar_hsa_circ_370443,RMVar_hsa_circ_193504 2465 RMVar_ID_2465 Human_SNP_ID_660508049 A-to-I Human chr19 + 18574177 18574177 18574177 ATGGTGGTGCGTGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGAAGGAGAATTGCTTGAACTCG ATGGTGGTGCGTGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGAAGGAGAATTGCTTGAACTCG A G UBA52 Ensembl:ENSG00000221983 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs964259608 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193498,RMVar_hsa_circ_96992,RMVar_hsa_circ_193500,RMVar_hsa_circ_75863,RMVar_hsa_circ_115874,RMVar_hsa_circ_193499,RMVar_hsa_circ_370443,RMVar_hsa_circ_193504 2466 RMVar_ID_2466 Human_SNP_ID_660508159 A-to-I Human chr19 + 18574430 18574430 18574430 CCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCACCCGCCACCACGCCCAGCTAATTTTTTT CCTGCCTCAGCCTCCCGAGTAGCTGGGATTACGGGCACCCGCCACCACGCCCAGCTAATTTTTTT A G UBA52 Ensembl:ENSG00000221983 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1231286259 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193498,RMVar_hsa_circ_96992,RMVar_hsa_circ_193500,RMVar_hsa_circ_75863,RMVar_hsa_circ_115874,RMVar_hsa_circ_193499,RMVar_hsa_circ_370443,RMVar_hsa_circ_193504 2467 RMVar_ID_2467 Human_SNP_ID_660508169 A-to-I Human chr19 + 18574481 18574480 18574482 CAGCTAATTTTTTTTGTATTTTTAGTAGAGACAGGGTTTCACTACGTTGGCCAGGCTGGTCTCTT CAGCTAATTTTTTTTGTATTTTTAGTAGAGAC__GGTTTCACTACGTTGGCCAGGCTGGTCTCTT CAG C UBA52 Ensembl:ENSG00000221983 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956968463 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_193498,RMVar_hsa_circ_96992,RMVar_hsa_circ_193500,RMVar_hsa_circ_75863,RMVar_hsa_circ_115874,RMVar_hsa_circ_193499,RMVar_hsa_circ_370443,RMVar_hsa_circ_193504 2468 RMVar_ID_2468 Human_SNP_ID_660508170 A-to-I Human chr19 + 18574481 18574481 18574481 CAGCTAATTTTTTTTGTATTTTTAGTAGAGACAGGGTTTCACTACGTTGGCCAGGCTGGTCTCTT CAGCTAATTTTTTTTGTATTTTTAGTAGAGACGGGGTTTCACTACGTTGGCCAGGCTGGTCTCTT A G UBA52 Ensembl:ENSG00000221983 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs922650014 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193498,RMVar_hsa_circ_96992,RMVar_hsa_circ_193500,RMVar_hsa_circ_75863,RMVar_hsa_circ_115874,RMVar_hsa_circ_193499,RMVar_hsa_circ_370443,RMVar_hsa_circ_193504 2469 RMVar_ID_2469 Human_SNP_ID_660516740 A-to-I Human chr19 - 18602794 18602794 18602794 GCCTGGGTGACAGAGTGAGACTCTGTCTCAAAAAAAAAAAAAAGTAGAACACTGAGTCAGGCTGG GCCTGGGTGACAGAGTGAGACTCTGTCTCAAAGAAAAAAAAAAGTAGAACACTGAGTCAGGCTGG T C CRLF1 Ensembl:ENSG00000006016 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs959349308 Functional Loss SNV dbSNP153 33..33 33 - - - 2470 RMVar_ID_2470 Human_SNP_ID_660541486 A-to-I Human chr19 + 18693207 18693207 18693207 GGTCAAGAGATCGAGACCACCCTGGGCAACATAGTGAAACTCTGTCTTTACTAAAAATACAAAAA GGTCAAGAGATCGAGACCACCCTGGGCAACATGGTGAAACTCTGTCTTTACTAAAAATACAAAAA A G CRTC1 Ensembl:ENSG00000105662 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1038063156 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13396047 2471 RMVar_ID_2471 Human_SNP_ID_660557763 A-to-I Human chr19 + 18752664 18752663 18752665 TCTCTCTTTCTTTCTTTTTTTTTTTTTGAAACAGAGTTTCACTCTGTCGCCCAGACTGGAGTGCA TCTCTCTTTCTTTCTTTTTTTTTTTTTGAAAC__AGTTTCACTCTGTCGCCCAGACTGGAGTGCA CAG C CRTC1 Ensembl:ENSG00000105662 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1247067210 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_2559371 RMVar_hsa_circ_86439,RMVar_hsa_circ_344588,RMVar_hsa_circ_193515,RMVar_hsa_circ_193516,RMVar_hsa_circ_109121,RMVar_hsa_circ_193517,RMVar_hsa_circ_283704 2472 RMVar_ID_2472 Human_SNP_ID_660557764 A-to-I Human chr19 + 18752664 18752664 18752664 TCTCTCTTTCTTTCTTTTTTTTTTTTTGAAACAGAGTTTCACTCTGTCGCCCAGACTGGAGTGCA TCTCTCTTTCTTTCTTTTTTTTTTTTTGAAACTGAGTTTCACTCTGTCGCCCAGACTGGAGTGCA A T CRTC1 Ensembl:ENSG00000105662 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1361884613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2559371 RMVar_hsa_circ_86439,RMVar_hsa_circ_344588,RMVar_hsa_circ_193515,RMVar_hsa_circ_193516,RMVar_hsa_circ_109121,RMVar_hsa_circ_193517,RMVar_hsa_circ_283704 2473 RMVar_ID_2473 Human_SNP_ID_660557909 A-to-I Human chr19 + 18753129 18753129 18753129 CTACTAAAAATAAAAAAAATAAAAAAAAAATTAGCCTGGCATCGTGGCGGGCACCTGTAGTCCCA CTACTAAAAATAAAAAAAATAAAAAAAAAATTCGCCTGGCATCGTGGCGGGCACCTGTAGTCCCA A C CRTC1 Ensembl:ENSG00000105662 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1329093925 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86439,RMVar_hsa_circ_344588,RMVar_hsa_circ_193515,RMVar_hsa_circ_193516,RMVar_hsa_circ_109121,RMVar_hsa_circ_193517,RMVar_hsa_circ_283704 2474 RMVar_ID_2474 Human_SNP_ID_660596164 A-to-I Human chr19 - 18882631 18882631 18882631 CTTATTTATTTACTTACTTATTTTTTTGAGACAGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCA CTTATTTATTTACTTACTTATTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCA T C GDF1,CERS1 Ensembl:ENSG00000130283,Ensembl:ENSG00000223802 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048364887 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_295181,RMVar_hsa_circ_193541 2475 RMVar_ID_2475 Human_SNP_ID_660596165 A-to-I Human chr19 - 18882631 18882631 18882631 CTTATTTATTTACTTACTTATTTTTTTGAGACAGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCA CTTATTTATTTACTTACTTATTTTTTTGAGACCGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCA T G GDF1,CERS1 Ensembl:ENSG00000130283,Ensembl:ENSG00000223802 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048364887 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_295181,RMVar_hsa_circ_193541 2476 RMVar_ID_2476 Human_SNP_ID_660604178 A-to-I Human chr19 - 18908850 18908850 18908850 GGGACTACAGGCACGCATCACCATGCCTGGCTAATTTGTATATTTTTTAGAGATGGGGTTTTGCC GGGACTACAGGCACGCATCACCATGCCTGGCTGATTTGTATATTTTTTAGAGATGGGGTTTTGCC T C AC002985.1,COPE Ensembl:ENSG00000268193,Ensembl:ENSG00000105669 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1204143988 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193546,RMVar_hsa_circ_86189,RMVar_hsa_circ_331899,RMVar_hsa_circ_193549,RMVar_hsa_circ_104727 2477 RMVar_ID_2477 Human_SNP_ID_660604191 A-to-I Human chr19 - 18908876 18908876 18908876 ATCCCACCTCAGCCTCCCGAATAGCTGGGACTACAGGCACGCATCACCATGCCTGGCTAATTTGT ATCCCACCTCAGCCTCCCGAATAGCTGGGACTGCAGGCACGCATCACCATGCCTGGCTAATTTGT T C AC002985.1,COPE Ensembl:ENSG00000268193,Ensembl:ENSG00000105669 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1010611822 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193546,RMVar_hsa_circ_86189,RMVar_hsa_circ_331899,RMVar_hsa_circ_193549,RMVar_hsa_circ_104727 2478 RMVar_ID_2478 Human_SNP_ID_660604213 A-to-I Human chr19 - 18908964 18908964 18908964 AGATACGGTCTTGCTCTGTCGTTCAGCCTGGCATACAGTGGCACAATCTTGGCTTACTGCAGCCT AGATACGGTCTTGCTCTGTCGTTCAGCCTGGCGTACAGTGGCACAATCTTGGCTTACTGCAGCCT T C AC002985.1,COPE Ensembl:ENSG00000268193,Ensembl:ENSG00000105669 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1359066350 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13397944,Human_RBP_ID_17567623,Human_RBP_ID_23310122,Human_RBP_ID_26985720 RMVar_hsa_circ_193546,RMVar_hsa_circ_86189,RMVar_hsa_circ_331899,RMVar_hsa_circ_193549,RMVar_hsa_circ_104727 2479 RMVar_ID_2479 Human_SNP_ID_660604383 A-to-I Human chr19 - 18909608 18909608 18909608 AGGCTGAGGCAGGAGAATCGCTTGAACCTGGCAGGCAGAGGTTGCAGTGAGCCAAGATCGCACTA AGGCTGAGGCAGGAGAATCGCTTGAACCTGGCGGGCAGAGGTTGCAGTGAGCCAAGATCGCACTA T C AC002985.1,COPE Ensembl:ENSG00000268193,Ensembl:ENSG00000105669 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053381529 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193546,RMVar_hsa_circ_86189,RMVar_hsa_circ_331899,RMVar_hsa_circ_193549,RMVar_hsa_circ_104727 2480 RMVar_ID_2480 Human_SNP_ID_660605756 A-to-I Human chr19 - 18914502 18914502 18914502 GAGTCTTGCTCTGTCACCTAGGCTGGAGTGCAATGGCGTGATCTCGGCTTACTACAGCCTCTATC GAGTCTTGCTCTGTCACCTAGGCTGGAGTGCAGTGGCGTGATCTCGGCTTACTACAGCCTCTATC T C AC002985.1,COPE Ensembl:ENSG00000268193,Ensembl:ENSG00000105669 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs975928190 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193546,RMVar_hsa_circ_86189 2481 RMVar_ID_2481 Human_SNP_ID_660608541 A-to-I Human chr19 + 18923260 18923260 18923260 GAGAAAAGTTGGGACTGGGTGCAGTGACTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGT GAGAAAAGTTGGGACTGGGTGCAGTGACTCACTCCTGTAATCCCAGCACTTTGGGAGGCCGAGGT A T DDX49 Ensembl:ENSG00000105671 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1313697694 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26515,RMVar_hsa_circ_101537,RMVar_hsa_circ_193553 2482 RMVar_ID_2482 Human_SNP_ID_660629188 A-to-I Human chr19 - 18996526 18996526 18996526 ACATCAAAAGCTGGGTGCAGTGGCACATACCTATAGTTCCAGTTAATGGGGAGACTGAGGTGGGA ACATCAAAAGCTGGGTGCAGTGGCACATACCTGTAGTTCCAGTTAATGGGGAGACTGAGGTGGGA T C SUGP2 Ensembl:ENSG00000064607 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs910984934 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47792,RMVar_hsa_circ_63450,RMVar_hsa_circ_6876,RMVar_hsa_circ_52054,RMVar_hsa_circ_22560,RMVar_hsa_circ_1434 2483 RMVar_ID_2483 Human_SNP_ID_660629224 A-to-I Human chr19 - 18996645 18996645 18996645 GGGAGGCTGAAGCAGGAGAATCGCTTGAACCCAGGAGGCGGAGGTTACAATGAGTTGAGATTGCA GGGAGGCTGAAGCAGGAGAATCGCTTGAACCCTGGAGGCGGAGGTTACAATGAGTTGAGATTGCA T A SUGP2 Ensembl:ENSG00000064607 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1568375525 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47792,RMVar_hsa_circ_63450,RMVar_hsa_circ_6876,RMVar_hsa_circ_52054,RMVar_hsa_circ_22560,RMVar_hsa_circ_1434 2484 RMVar_ID_2484 Human_SNP_ID_660629255 A-to-I Human chr19 - 18996753 18996753 18996753 TCAGGAGTTTGATCAAGACCAGCATGGTTAACATGGCGAAACCCCGTCTCTACTAAAAATACAAA TCAGGAGTTTGATCAAGACCAGCATGGTTAACGTGGCGAAACCCCGTCTCTACTAAAAATACAAA T C SUGP2 Ensembl:ENSG00000064607 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1326135219 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47792,RMVar_hsa_circ_63450,RMVar_hsa_circ_6876,RMVar_hsa_circ_52054,RMVar_hsa_circ_22560,RMVar_hsa_circ_1434 2485 RMVar_ID_2485 Human_SNP_ID_660629279 A-to-I Human chr19 - 18996845 18996845 18996845 AAATGCCTTAAATAAATACATCAGCCAGGCGCAGTGGCTCATGCCTGTAATCCCAGCACTTTGTG AAATGCCTTAAATAAATACATCAGCCAGGCGCTGTGGCTCATGCCTGTAATCCCAGCACTTTGTG T A SUGP2 Ensembl:ENSG00000064607 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs941439861 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47792,RMVar_hsa_circ_63450,RMVar_hsa_circ_6876,RMVar_hsa_circ_52054,RMVar_hsa_circ_22560,RMVar_hsa_circ_1434 2486 RMVar_ID_2486 Human_SNP_ID_660629710 A-to-I Human chr19 - 18998425 18998425 18998425 ATAAAAAAAGGTGTGCGGTGGCTTACACCTGTAATCCCGGGACTTTGGAAGGCCAAGGCAGGGGG ATAAAAAAAGGTGTGCGGTGGCTTACACCTGTGATCCCGGGACTTTGGAAGGCCAAGGCAGGGGG T C SUGP2 Ensembl:ENSG00000064607 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917093579 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20363341 RMVar_hsa_circ_47792,RMVar_hsa_circ_63450,RMVar_hsa_circ_6876,RMVar_hsa_circ_52054,RMVar_hsa_circ_22560,RMVar_hsa_circ_1434 2487 RMVar_ID_2487 Human_SNP_ID_660629712 A-to-I Human chr19 - 18998431 18998429 18998431 AACAGGATAAAAAAAGGTGTGCGGTGGCTTACACCTGTAATCCCGGGACTTTGGAAGGCCAAGGC AACAGGATAAAAAAAGGTGTGCGGTGGCTTAC__CTGTAATCCCGGGACTTTGGAAGGCCAAGGC GGT G SUGP2 Ensembl:ENSG00000064607 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs948585781 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_47792,RMVar_hsa_circ_63450,RMVar_hsa_circ_6876,RMVar_hsa_circ_52054,RMVar_hsa_circ_22560,RMVar_hsa_circ_1434 2488 RMVar_ID_2488 Human_SNP_ID_660630312 A-to-I Human chr19 - 19000844 19000844 19000844 AAAATTAGTTGGGCATGGTGGTGCATGCCTGTAGTCCCAGCTACTCTGGAGGCTGAGGTGGAAGG AAAATTAGTTGGGCATGGTGGTGCATGCCTGTGGTCCCAGCTACTCTGGAGGCTGAGGTGGAAGG T C SUGP2 Ensembl:ENSG00000064607 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1306569417 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47792,RMVar_hsa_circ_63450,RMVar_hsa_circ_6876,RMVar_hsa_circ_52054,RMVar_hsa_circ_22560,RMVar_hsa_circ_343820,RMVar_hsa_circ_1434 2489 RMVar_ID_2489 Human_SNP_ID_660630662 A-to-I Human chr19 - 19002297 19002297 19002297 CGGCTCACTACAACCTCTGCCTCCCGGGTTCAAGTTATTCTCCTGCCTCAGCCTCCTGAATAGCT CGGCTCACTACAACCTCTGCCTCCCGGGTTCAGGTTATTCTCCTGCCTCAGCCTCCTGAATAGCT T C SUGP2 Ensembl:ENSG00000064607 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs953426187 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47792,RMVar_hsa_circ_63450,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 2490 RMVar_ID_2490 Human_SNP_ID_660630814 A-to-I Human chr19 - 19002695 19002695 19002695 CAGCCTGACCAACATGGAGATATCCCATCTCTACTAAAAATACAGAATTAGCGAGGCGTGGTGAC CAGCCTGACCAACATGGAGATATCCCATCTCTTCTAAAAATACAGAATTAGCGAGGCGTGGTGAC T A SUGP2 Ensembl:ENSG00000064607 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1307310086 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47792,RMVar_hsa_circ_63450,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 2491 RMVar_ID_2491 Human_SNP_ID_660630836 A-to-I Human chr19 - 19002792 19002792 19002792 AAACCAGACCTGCGCCGGGTGTGCTGGCTCACACCTGTAATCCCAGCACTCTGGGAGGCCAAGGC AAACCAGACCTGCGCCGGGTGTGCTGGCTCACGCCTGTAATCCCAGCACTCTGGGAGGCCAAGGC T C SUGP2 Ensembl:ENSG00000064607 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs778615325 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47792,RMVar_hsa_circ_63450,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 2492 RMVar_ID_2492 Human_SNP_ID_660631695 A-to-I Human chr19 - 19005829 19005829 19005829 TGTGTGTGTGTGTGTGTTTGTTAGCCTGGTATAGTGGCATTTGCCTGTGGTCCTAACTACTTGGG TGTGTGTGTGTGTGTGTTTGTTAGCCTGGTATGGTGGCATTTGCCTGTGGTCCTAACTACTTGGG T C SUGP2 Ensembl:ENSG00000064607 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1362673254 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_516626,Human_RBP_ID_1093765,Human_RBP_ID_5292766,Human_RBP_ID_5650023,Human_RBP_ID_17272089,Human_RBP_ID_23787198 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_347485,RMVar_hsa_circ_332124,RMVar_hsa_circ_312658,RMVar_hsa_circ_193566 2493 RMVar_ID_2493 Human_SNP_ID_660636542 A-to-I Human chr19 - 19023664 19023664 19023664 GAACTCCTGAGCTCAAGTGATCTACCTGCCTCAGCCTCCCAAAGTGCTGGGATTATAGGTGTGAG GAACTCCTGAGCTCAAGTGATCTACCTGCCTCCGCCTCCCAAAGTGCTGGGATTATAGGTGTGAG T G SUGP2 Ensembl:ENSG00000064607 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1164305571 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1505,RMVar_hsa_circ_121444,RMVar_hsa_circ_1434,RMVar_hsa_circ_332124,RMVar_hsa_circ_193566,RMVar_hsa_circ_348184,RMVar_hsa_circ_11075,RMVar_hsa_circ_288168,RMVar_hsa_circ_56627,RMVar_hsa_circ_193570 2494 RMVar_ID_2494 Human_SNP_ID_660638737 A-to-I Human chr19 - 19031157 19031157 19031157 GTGATCCGCCCACCTCGACCTCCCAAAGTGCCAGGATTACAGGTATGAGCCACCGCGCCCAGCTC GTGATCCGCCCACCTCGACCTCCCAAAGTGCCGGGATTACAGGTATGAGCCACCGCGCCCAGCTC T C SUGP2 Ensembl:ENSG00000064607 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1241188094 Functional Loss SNV dbSNP153 33..33 33 - - - 2495 RMVar_ID_2495 Human_SNP_ID_660640649 A-to-I Human chr19 + 19037502 19037502 19037502 TGGGCTCCCACCTCAGCCTCCCAAATAGCTGTAACTACAGGTGCATGCTCCCACACCTGGCTAAT TGGGCTCCCACCTCAGCCTCCCAAATAGCTGTGACTACAGGTGCATGCTCCCACACCTGGCTAAT A G ARMC6 Ensembl:ENSG00000105676 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992132866 Functional Loss SNV dbSNP153 33..33 33 - - - 2496 RMVar_ID_2496 Human_SNP_ID_660643936 A-to-I Human chr19 + 19049903 19049903 19049903 AAAATTATCCGGGCGTGGTGGCACATGCCTGTAGTCCCAGCTGCTCAGGAGGCTGAAGCGGGAGG AAAATTATCCGGGCGTGGTGGCACATGCCTGTCGTCCCAGCTGCTCAGGAGGCTGAAGCGGGAGG A C ARMC6 Ensembl:ENSG00000105676 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1373022771 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69651,RMVar_hsa_circ_280440,RMVar_hsa_circ_81496,RMVar_hsa_circ_193575,RMVar_hsa_circ_193576,RMVar_hsa_circ_193577,RMVar_hsa_circ_103675 2497 RMVar_ID_2497 Human_SNP_ID_660646096 A-to-I Human chr19 + 19057459 19057459 19057459 CATGCTGATCCGAAACCTGGTGGCCCACGGCCAGGCCTTCTCGAAGCCCATCCTGGACCTGGGGG CATGCTGATCCGAAACCTGGTGGCCCACGGCCGGGCCTTCTCGAAGCCCATCCTGGACCTGGGGG A G ARMC6 Ensembl:ENSG00000105676 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1207393083 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5116820 Human_Splice_Rec_1982054,Human_Splice_Rec_1982082,Human_Splice_Rec_1982102,Human_Splice_Rec_1982112,Human_Splice_Rec_1982182,Human_Splice_Rec_1982194,Human_Splice_Rec_1982200,Human_Splice_Rec_1982202 RMVar_hsa_circ_45084,RMVar_hsa_circ_193577,RMVar_hsa_circ_103675,RMVar_hsa_circ_112597,RMVar_hsa_circ_193581 2498 RMVar_ID_2498 Human_SNP_ID_660656582 A-to-I Human chr19 + 19100177 19100177 19100177 CAGCCTGGCCAACATGGCGAAACCTCATTTCTACTAAAAATACAAAAATTAGCCAGGCGTGGTGG CAGCCTGGCCAACATGGCGAAACCTCATTTCTGCTAAAAATACAAAAATTAGCCAGGCGTGGTGG A G SLC25A42 Ensembl:ENSG00000181035 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs554646192 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57174 2499 RMVar_ID_2499 Human_SNP_ID_660656591 A-to-I Human chr19 + 19100231 19100231 19100231 AGGCGTGGTGGTGCTTGCCTGTAATTCCAGCTACTCAGGAGGCTGAGGGAGGAGAATCGCTTGAA AGGCGTGGTGGTGCTTGCCTGTAATTCCAGCTTCTCAGGAGGCTGAGGGAGGAGAATCGCTTGAA A T SLC25A42 Ensembl:ENSG00000181035 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1457882682 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57174 2500 RMVar_ID_2500 Human_SNP_ID_660657321 A-to-I Human chr19 + 19103088 19103088 19103088 GTCTGTTTTCTCTCTCTCTCTTTTATTTATTTATTTTTGTTTGTTTGTTTGTTTTTGAGATAGAG GTCTGTTTTCTCTCTCTCTCTTTTATTTATTTTTTTTTGTTTGTTTGTTTGTTTTTGAGATAGAG A T SLC25A42 Ensembl:ENSG00000181035 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1010096606 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57174,RMVar_hsa_circ_70018 2501 RMVar_ID_2501 Human_SNP_ID_660660995 A-to-I Human chr19 - 19116683 19116683 19116683 GGTTTTTGTTGTTGTTGTTGTTGTTTTGCGACAGGGTCTGGTTCTATCACCCATGCTGGGATGCA GGTTTTTGTTGTTGTTGTTGTTGTTTTGCGACGGGGTCTGGTTCTATCACCCATGCTGGGATGCA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984088627 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3564812 2502 RMVar_ID_2502 Human_SNP_ID_660666167 A-to-I Human chr19 - 19135724 19135724 19135724 AAATAGACAAAAATTAGTTGGGTATGGTGGCGAGTGCCTGTAATCCCAGCTACTAGGGAGGCTGA AAATAGACAAAAATTAGTTGGGTATGGTGGCGCGTGCCTGTAATCCCAGCTACTAGGGAGGCTGA T G TMEM161A Ensembl:ENSG00000064545 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1454965986 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193591,RMVar_hsa_circ_108555 2503 RMVar_ID_2503 Human_SNP_ID_660666183 A-to-I Human chr19 - 19135803 19135803 19135803 GGGAGGCCAAGGCAGGAGGATTGCTTGAGCCTAGGAGTTCAAGACCAGCCTGGCAACATGGAGAA GGGAGGCCAAGGCAGGAGGATTGCTTGAGCCTGGGAGTTCAAGACCAGCCTGGCAACATGGAGAA T C TMEM161A Ensembl:ENSG00000064545 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1012568095 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193591,RMVar_hsa_circ_108555 2504 RMVar_ID_2504 Human_SNP_ID_660666191 A-to-I Human chr19 - 19135849 19135849 19135849 AAAATAGGCCGGACACAGTGGCTCACGCCTGTAATCCCAACCGTTTGGGAGGCCAAGGCAGGAGG AAAATAGGCCGGACACAGTGGCTCACGCCTGTGATCCCAACCGTTTGGGAGGCCAAGGCAGGAGG T C TMEM161A Ensembl:ENSG00000064545 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs971595420 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193591,RMVar_hsa_circ_108555 2505 RMVar_ID_2505 Human_SNP_ID_660673605 A-to-I Human chr19 - 19164566 19164566 19164566 CAAGTGATCTGCCCACCTCGGTCTCCCAAAGTAGTGGGATTACAGGCGTGAGCCACCGCACCCGG CAAGTGATCTGCCCACCTCGGTCTCCCAAAGTTGTGGGATTACAGGCGTGAGCCACCGCACCCGG T A MEF2B,BORCS8-MEF2B Ensembl:ENSG00000213999,Ensembl:ENSG00000064489 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1179686554 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106768,RMVar_hsa_circ_193593 2506 RMVar_ID_2506 Human_SNP_ID_660675367 A-to-I Human chr19 - 19171541 19171540 19171542 GCCCAGGAGTTTGGGACCAGCCTGGGCAACATAGTGAGACATCCTCTCTTAAAAAAAACAAAATT GCCCAGGAGTTTGGGACCAGCCTGGGCAACA__GTGAGACATCCTCTCTTAAAAAAAACAAAATT CTA C MEF2B,BORCS8-MEF2B Ensembl:ENSG00000213999,Ensembl:ENSG00000064489 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749630676 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_106768,RMVar_hsa_circ_193593 2507 RMVar_ID_2507 Human_SNP_ID_660675942 A-to-I Human chr19 - 19173719 19173719 19173719 GGTAGATGGAAGCGAGAGGATCACTTGAGCCCAGGAGTTCAAGGCTGCAGTGAGCCATGATTGTA GGTAGATGGAAGCGAGAGGATCACTTGAGCCCGGGAGTTCAAGGCTGCAGTGAGCCATGATTGTA T C MEF2B,BORCS8-MEF2B Ensembl:ENSG00000213999,Ensembl:ENSG00000064489 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054847186 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106768,RMVar_hsa_circ_193593 2508 RMVar_ID_2508 Human_SNP_ID_660676196 A-to-I Human chr19 - 19174563 19174563 19174563 CGTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCTGGCTGTGGTGAGCA CGTGGCCAACATGGTGAAACCCCATCTCTACTGAAAATACAAAAATTAGCTGGCTGTGGTGAGCA T C MEF2B,BORCS8-MEF2B Ensembl:ENSG00000213999,Ensembl:ENSG00000064489 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569867862 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106768,RMVar_hsa_circ_193593 2509 RMVar_ID_2509 Human_SNP_ID_660676276 A-to-I Human chr19 - 19174900 19174900 19174900 CGGAGGCCGAGGTGGGCGGATCACTTGACGTCAGGAGTTGGAGACCAGCCTGGCCAACATGATGA CGGAGGCCGAGGTGGGCGGATCACTTGACGTCGGGAGTTGGAGACCAGCCTGGCCAACATGATGA T C MEF2B,BORCS8-MEF2B Ensembl:ENSG00000213999,Ensembl:ENSG00000064489 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1210525035 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106768,RMVar_hsa_circ_193593 2510 RMVar_ID_2510 Human_SNP_ID_660676597 A-to-I Human chr19 - 19176082 19176082 19176082 CTCTCTCTCTTTTTTTTTTGAGCTGGAGCCTCACTCTCGCCCAGGCTGGAGTGCAGTGGCGCGAT CTCTCTCTCTTTTTTTTTTGAGCTGGAGCCTCGCTCTCGCCCAGGCTGGAGTGCAGTGGCGCGAT T C MEF2B,BORCS8-MEF2B Ensembl:ENSG00000213999,Ensembl:ENSG00000064489 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917009425 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106768,RMVar_hsa_circ_193593 2511 RMVar_ID_2511 Human_SNP_ID_660676724 A-to-I Human chr19 + 19176533 19176530 19176533 TAATGGCACAGAGGCCCCCCAGTGTGACCTAGAAGGAGGAGAGGTAGGGCTGAACCCCCTTTCCA TAATGGCACAGAGGCCCCCCAGTGTGACCT___AGGAGGAGAGGTAGGGCTGAACCCCCTTTCCA TAGA T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs940336578 Functional Loss DEL dbSNP153 31..33 33 - - - 2512 RMVar_ID_2512 Human_SNP_ID_660676726 A-to-I Human chr19 + 19176533 19176533 19176533 TAATGGCACAGAGGCCCCCCAGTGTGACCTAGAAGGAGGAGAGGTAGGGCTGAACCCCCTTTCCA TAATGGCACAGAGGCCCCCCAGTGTGACCTAGGAGGAGGAGAGGTAGGGCTGAACCCCCTTTCCA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs369948701 Functional Loss SNV dbSNP153 33..33 33 - - - 2513 RMVar_ID_2513 Human_SNP_ID_660676957 A-to-I Human chr19 - 19177445 19177445 19177445 TTTTGTATTTTTTGTAGAGACGGGGTTTCACCATGTTGGCTAGGCTGGTCTCAAACTCCTGAGCT TTTTGTATTTTTTGTAGAGACGGGGTTTCACCGTGTTGGCTAGGCTGGTCTCAAACTCCTGAGCT T C BORCS8,MEF2B,BORCS8-MEF2B Ensembl:ENSG00000254901,Ensembl:ENSG00000213999,Ensembl:ENSG00000064489 Protein coding,Protein coding,Protein coding 3'UTR,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1035466453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25389996 Human_Splice_Rec_1982638,Human_Splice_Rec_1982644,Human_Splice_Rec_1982654,Human_Splice_Rec_1982670 RMVar_hsa_circ_104466,RMVar_hsa_circ_106768,RMVar_hsa_circ_193593,RMVar_hsa_circ_108817,RMVar_hsa_circ_193595,RMVar_hsa_circ_193597,RMVar_hsa_circ_99317,RMVar_hsa_circ_193596 2514 RMVar_ID_2514 Human_SNP_ID_660676958 A-to-I Human chr19 - 19177445 19177445 19177445 TTTTGTATTTTTTGTAGAGACGGGGTTTCACCATGTTGGCTAGGCTGGTCTCAAACTCCTGAGCT TTTTGTATTTTTTGTAGAGACGGGGTTTCACCCTGTTGGCTAGGCTGGTCTCAAACTCCTGAGCT T G BORCS8,MEF2B,BORCS8-MEF2B Ensembl:ENSG00000254901,Ensembl:ENSG00000213999,Ensembl:ENSG00000064489 Protein coding,Protein coding,Protein coding 3'UTR,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1035466453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25389996 Human_Splice_Rec_1982638,Human_Splice_Rec_1982644,Human_Splice_Rec_1982654,Human_Splice_Rec_1982670 RMVar_hsa_circ_104466,RMVar_hsa_circ_106768,RMVar_hsa_circ_193593,RMVar_hsa_circ_108817,RMVar_hsa_circ_193595,RMVar_hsa_circ_193597,RMVar_hsa_circ_99317,RMVar_hsa_circ_193596 2515 RMVar_ID_2515 Human_SNP_ID_660677432 A-to-I Human chr19 - 19177952 19177952 19177952 TTGAACCCAGGAGGCAGAGGTTCCAGTGAGCCAAGATGGCGCCACTGCACTCCAGCCTGCGCGAC TTGAACCCAGGAGGCAGAGGTTCCAGTGAGCCGAGATGGCGCCACTGCACTCCAGCCTGCGCGAC T C BORCS8,MEF2B,BORCS8-MEF2B Ensembl:ENSG00000254901,Ensembl:ENSG00000213999,Ensembl:ENSG00000064489 Protein coding,Protein coding,Protein coding intron,intron,intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1432403865 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104466,RMVar_hsa_circ_106768,RMVar_hsa_circ_193593,RMVar_hsa_circ_108817,RMVar_hsa_circ_193595,RMVar_hsa_circ_193597,RMVar_hsa_circ_99317,RMVar_hsa_circ_193596 2516 RMVar_ID_2516 Human_SNP_ID_660677449 A-to-I Human chr19 - 19178008 19178008 19178008 GTGATGGCGGGCACCTGTAATCCCAGCTACTCAGGAGGTTGAGGCATGAGAATCGCTTGAACCCA GTGATGGCGGGCACCTGTAATCCCAGCTACTCGGGAGGTTGAGGCATGAGAATCGCTTGAACCCA T C BORCS8,MEF2B,BORCS8-MEF2B Ensembl:ENSG00000254901,Ensembl:ENSG00000213999,Ensembl:ENSG00000064489 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229 RNA-Seq:(High) rs1313109136 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104466,RMVar_hsa_circ_106768,RMVar_hsa_circ_193593,RMVar_hsa_circ_108817,RMVar_hsa_circ_193595,RMVar_hsa_circ_193597,RMVar_hsa_circ_99317,RMVar_hsa_circ_193596 2517 RMVar_ID_2517 Human_SNP_ID_660677668 A-to-I Human chr19 - 19178838 19178838 19178838 ATCCCGCTTCAGCCTCCCGAGTAGGTGGGACTACAGGTGCCTGCCACCTCGCCCGGCTAATTTTT ATCCCGCTTCAGCCTCCCGAGTAGGTGGGACTGCAGGTGCCTGCCACCTCGCCCGGCTAATTTTT T C BORCS8,MEF2B,BORCS8-MEF2B Ensembl:ENSG00000254901,Ensembl:ENSG00000213999,Ensembl:ENSG00000064489 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs1039520246 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104466,RMVar_hsa_circ_106768,RMVar_hsa_circ_193593,RMVar_hsa_circ_108817,RMVar_hsa_circ_193595,RMVar_hsa_circ_193597,RMVar_hsa_circ_99317,RMVar_hsa_circ_193596 2518 RMVar_ID_2518 Human_SNP_ID_660677669 A-to-I Human chr19 - 19178838 19178838 19178838 ATCCCGCTTCAGCCTCCCGAGTAGGTGGGACTACAGGTGCCTGCCACCTCGCCCGGCTAATTTTT ATCCCGCTTCAGCCTCCCGAGTAGGTGGGACTCCAGGTGCCTGCCACCTCGCCCGGCTAATTTTT T G BORCS8,MEF2B,BORCS8-MEF2B Ensembl:ENSG00000254901,Ensembl:ENSG00000213999,Ensembl:ENSG00000064489 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs1039520246 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104466,RMVar_hsa_circ_106768,RMVar_hsa_circ_193593,RMVar_hsa_circ_108817,RMVar_hsa_circ_193595,RMVar_hsa_circ_193597,RMVar_hsa_circ_99317,RMVar_hsa_circ_193596 2519 RMVar_ID_2519 Human_SNP_ID_660677683 A-to-I Human chr19 - 19178897 19178897 19178897 AGAGTGCGGTGGTGCGATCTCGGTTCAGTGTAACCTCTGCCTGTCAGGTTCAAGCGATTATCCCG AGAGTGCGGTGGTGCGATCTCGGTTCAGTGTACCCTCTGCCTGTCAGGTTCAAGCGATTATCCCG T G BORCS8,MEF2B,BORCS8-MEF2B Ensembl:ENSG00000254901,Ensembl:ENSG00000213999,Ensembl:ENSG00000064489 Protein coding,Protein coding,Protein coding 3'UTR,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1450531574 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1982637 RMVar_hsa_circ_104466,RMVar_hsa_circ_106768,RMVar_hsa_circ_193593,RMVar_hsa_circ_108817,RMVar_hsa_circ_193595,RMVar_hsa_circ_193597,RMVar_hsa_circ_99317,RMVar_hsa_circ_193596 2520 RMVar_ID_2520 Human_SNP_ID_660680080 A-to-I Human chr19 - 19187569 19187569 19187569 GCACCACTGCACTCCAGCCTGATGACAGAGCAAGACTCTGTCTCAAAAAAAAAAAAAAGAAGTTT GCACCACTGCACTCCAGCCTGATGACAGAGCAGGACTCTGTCTCAAAAAAAAAAAAAAGAAGTTT T C BORCS8,MEF2B,BORCS8-MEF2B Ensembl:ENSG00000254901,Ensembl:ENSG00000213999,Ensembl:ENSG00000064489 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1371530678 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104466,RMVar_hsa_circ_193597 2521 RMVar_ID_2521 Human_SNP_ID_660680294 A-to-I Human chr19 - 19188231 19188231 19188231 AGGTCAGGAGATCGAGACCATCCTGGTAACACAGTGAAACCCCGTCTCTACTAAAAAATACAAAA AGGTCAGGAGATCGAGACCATCCTGGTAACACGGTGAAACCCCGTCTCTACTAAAAAATACAAAA T C BORCS8,MEF2B,BORCS8-MEF2B Ensembl:ENSG00000254901,Ensembl:ENSG00000213999,Ensembl:ENSG00000064489 Protein coding,Protein coding,Protein coding intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs868309188 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104466,RMVar_hsa_circ_193597 2522 RMVar_ID_2522 Human_SNP_ID_660680306 A-to-I Human chr19 - 19188275 19188275 19188275 GCCTGTAATCCCAGCACTTTGGAGCCCGAGGCAGGCGGATCACGAGGTCAGGAGATCGAGACCAT GCCTGTAATCCCAGCACTTTGGAGCCCGAGGCTGGCGGATCACGAGGTCAGGAGATCGAGACCAT T A BORCS8,MEF2B,BORCS8-MEF2B Ensembl:ENSG00000254901,Ensembl:ENSG00000213999,Ensembl:ENSG00000064489 Protein coding,Protein coding,Protein coding intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs762870335 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104466,RMVar_hsa_circ_193597 2523 RMVar_ID_2523 Human_SNP_ID_660680307 A-to-I Human chr19 - 19188275 19188275 19188275 GCCTGTAATCCCAGCACTTTGGAGCCCGAGGCAGGCGGATCACGAGGTCAGGAGATCGAGACCAT GCCTGTAATCCCAGCACTTTGGAGCCCGAGGCGGGCGGATCACGAGGTCAGGAGATCGAGACCAT T C BORCS8,MEF2B,BORCS8-MEF2B Ensembl:ENSG00000254901,Ensembl:ENSG00000213999,Ensembl:ENSG00000064489 Protein coding,Protein coding,Protein coding intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs762870335 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104466,RMVar_hsa_circ_193597 2524 RMVar_ID_2524 Human_SNP_ID_660680357 A-to-I Human chr19 - 19188433 19188433 19188433 TCACTGGGGGCCAGGCACAGTGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCTGAGGCAGGA TCACTGGGGGCCAGGCACAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGA T C BORCS8,MEF2B,BORCS8-MEF2B Ensembl:ENSG00000254901,Ensembl:ENSG00000213999,Ensembl:ENSG00000064489 Protein coding,Protein coding,Protein coding intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1425036950 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104466,RMVar_hsa_circ_193597 2525 RMVar_ID_2525 Human_SNP_ID_660680755 A-to-I Human chr19 - 19189817 19189817 19189817 CACTTGTCAGACCCAAGCAGTCCTCCCACCTCAGCCTCCTGAGTAGCTGGGACTACAGGTATAGA CACTTGTCAGACCCAAGCAGTCCTCCCACCTCGGCCTCCTGAGTAGCTGGGACTACAGGTATAGA T C BORCS8,MEF2B,BORCS8-MEF2B Ensembl:ENSG00000254901,Ensembl:ENSG00000213999,Ensembl:ENSG00000064489 Protein coding,Protein coding,Protein coding intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1441252719 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104466,RMVar_hsa_circ_193597 2526 RMVar_ID_2526 Human_SNP_ID_660681086 A-to-I Human chr19 - 19191156 19191156 19191156 TAGAGACGGGGTTTCACCTTGTTGCTCAGGCTAGTCTCGAACTCCTGACCTCGAGTGATCCACCC TAGAGACGGGGTTTCACCTTGTTGCTCAGGCTCGTCTCGAACTCCTGACCTCGAGTGATCCACCC T G BORCS8,MEF2B,BORCS8-MEF2B Ensembl:ENSG00000254901,Ensembl:ENSG00000213999,Ensembl:ENSG00000064489 Protein coding,Protein coding,Protein coding intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1382910095 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104466,RMVar_hsa_circ_193597 2527 RMVar_ID_2527 Human_SNP_ID_660681109 A-to-I Human chr19 - 19191239 19191239 19191239 AGCTCACTGCAACCTCAGCCCCCTGAGTAGCTAGGATTACAGGCACACACCCCCATGCCCAGCTA AGCTCACTGCAACCTCAGCCCCCTGAGTAGCTGGGATTACAGGCACACACCCCCATGCCCAGCTA T C BORCS8,MEF2B,BORCS8-MEF2B Ensembl:ENSG00000254901,Ensembl:ENSG00000213999,Ensembl:ENSG00000064489 Protein coding,Protein coding,Protein coding intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1359406788 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104466,RMVar_hsa_circ_193597 2528 RMVar_ID_2528 Human_SNP_ID_660681143 A-to-I Human chr19 - 19191367 19191367 19191367 TTGCCTCAGCTTCTCCAGTAGCTGGGACTACAAGTGCACACCACCACATCAGGCTAATTCTTTAA TTGCCTCAGCTTCTCCAGTAGCTGGGACTACAGGTGCACACCACCACATCAGGCTAATTCTTTAA T C BORCS8,MEF2B,BORCS8-MEF2B Ensembl:ENSG00000254901,Ensembl:ENSG00000213999,Ensembl:ENSG00000064489 Protein coding,Protein coding,Protein coding intron,intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs999463044 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104466,RMVar_hsa_circ_193597 2529 RMVar_ID_2529 Human_SNP_ID_660681254 A-to-I Human chr19 - 19191696 19191696 19191696 GCACGCCTGTGGTCCCAGCTACTTGGGCGGCTAAGGTGGGAGGATTGCTTGAGCCCGGGAGGTCA GCACGCCTGTGGTCCCAGCTACTTGGGCGGCTGAGGTGGGAGGATTGCTTGAGCCCGGGAGGTCA T C BORCS8,MEF2B,BORCS8-MEF2B Ensembl:ENSG00000254901,Ensembl:ENSG00000213999,Ensembl:ENSG00000064489 Protein coding,Protein coding,Protein coding intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs145426713 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104466,RMVar_hsa_circ_193597 2530 RMVar_ID_2530 Human_SNP_ID_660681258 A-to-I Human chr19 - 19191708 19191708 19191708 GGGCGTGGTGGCGCACGCCTGTGGTCCCAGCTACTTGGGCGGCTAAGGTGGGAGGATTGCTTGAG GGGCGTGGTGGCGCACGCCTGTGGTCCCAGCTCCTTGGGCGGCTAAGGTGGGAGGATTGCTTGAG T G BORCS8,MEF2B,BORCS8-MEF2B Ensembl:ENSG00000254901,Ensembl:ENSG00000213999,Ensembl:ENSG00000064489 Protein coding,Protein coding,Protein coding intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs182259484 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104466,RMVar_hsa_circ_193597 2531 RMVar_ID_2531 Human_SNP_ID_660681268 A-to-I Human chr19 - 19191744 19191744 19191744 TGAGATCTCGTCTCTAAAAAAATACAAAAATTAGCCGGGCGTGGTGGCGCACGCCTGTGGTCCCA TGAGATCTCGTCTCTAAAAAAATACAAAAATTGGCCGGGCGTGGTGGCGCACGCCTGTGGTCCCA T C BORCS8,MEF2B,BORCS8-MEF2B Ensembl:ENSG00000254901,Ensembl:ENSG00000213999,Ensembl:ENSG00000064489 Protein coding,Protein coding,Protein coding intron,intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1053191977 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104466,RMVar_hsa_circ_193597 2532 RMVar_ID_2532 Human_SNP_ID_660681298 A-to-I Human chr19 - 19191858 19191858 19191858 ATTGTTTCAAGAATTCAGTAGCTGAGGCTGGGAGTGGTGGCTTTGTAATCCCAGCACTTTGGGAG ATTGTTTCAAGAATTCAGTAGCTGAGGCTGGGCGTGGTGGCTTTGTAATCCCAGCACTTTGGGAG T G BORCS8,MEF2B,BORCS8-MEF2B Ensembl:ENSG00000254901,Ensembl:ENSG00000213999,Ensembl:ENSG00000064489 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs997956257 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104466,RMVar_hsa_circ_193597 2533 RMVar_ID_2533 Human_SNP_ID_660708350 A-to-I Human chr19 - 19288138 19288138 19288138 CTGCCTCTTTATTTTTGAGACAGTTTCACTCTATTGCCCAGGCTGTAGTGCAATGGCATGATCTC CTGCCTCTTTATTTTTGAGACAGTTTCACTCTTTTGCCCAGGCTGTAGTGCAATGGCATGATCTC T A SUGP1 Ensembl:ENSG00000105705 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs763817373 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13401149 RMVar_hsa_circ_90731,RMVar_hsa_circ_193615,RMVar_hsa_circ_81399,RMVar_hsa_circ_193616 2534 RMVar_ID_2534 Human_SNP_ID_660708351 A-to-I Human chr19 - 19288138 19288138 19288138 CTGCCTCTTTATTTTTGAGACAGTTTCACTCTATTGCCCAGGCTGTAGTGCAATGGCATGATCTC CTGCCTCTTTATTTTTGAGACAGTTTCACTCTGTTGCCCAGGCTGTAGTGCAATGGCATGATCTC T C SUGP1 Ensembl:ENSG00000105705 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs763817373 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13401149 RMVar_hsa_circ_90731,RMVar_hsa_circ_193615,RMVar_hsa_circ_81399,RMVar_hsa_circ_193616 2535 RMVar_ID_2535 Human_SNP_ID_660708352 A-to-I Human chr19 - 19288138 19288138 19288138 CTGCCTCTTTATTTTTGAGACAGTTTCACTCTATTGCCCAGGCTGTAGTGCAATGGCATGATCTC CTGCCTCTTTATTTTTGAGACAGTTTCACTCTCTTGCCCAGGCTGTAGTGCAATGGCATGATCTC T G SUGP1 Ensembl:ENSG00000105705 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs763817373 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13401149 RMVar_hsa_circ_90731,RMVar_hsa_circ_193615,RMVar_hsa_circ_81399,RMVar_hsa_circ_193616 2536 RMVar_ID_2536 Human_SNP_ID_660708369 A-to-I Human chr19 - 19288234 19288234 19288234 ACGAGTCCAGGAATTTGAGGCTGCAGTGAGCTATGATCGTGGCACTGCACTCCAGCCTAGATGAC ACGAGTCCAGGAATTTGAGGCTGCAGTGAGCTGTGATCGTGGCACTGCACTCCAGCCTAGATGAC T C SUGP1 Ensembl:ENSG00000105705 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1455861927 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90731,RMVar_hsa_circ_193615,RMVar_hsa_circ_81399,RMVar_hsa_circ_193616 2537 RMVar_ID_2537 Human_SNP_ID_660708686 A-to-I Human chr19 - 19289564 19289564 19289564 TTTTTGGTTTTAGTAGAGACGAGGTTTCACCAAGTTGGCCAGACTGATCTTGAACTCCTGACCTC TTTTTGGTTTTAGTAGAGACGAGGTTTCACCAGGTTGGCCAGACTGATCTTGAACTCCTGACCTC T C SUGP1 Ensembl:ENSG00000105705 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1240266789 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90731,RMVar_hsa_circ_193615,RMVar_hsa_circ_81399,RMVar_hsa_circ_193616 2538 RMVar_ID_2538 Human_SNP_ID_660709729 A-to-I Human chr19 - 19293573 19293572 19293574 TCACTTCTTCTTGTTCTTTTTTTTTTTGAGACAGAGTCTTTCTCTGATGTGCAGGCTGGAGTGGT TCACTTCTTCTTGTTCTTTTTTTTTTTGAGA__GAGTCTTTCTCTGATGTGCAGGCTGGAGTGGT CTG C SUGP1 Ensembl:ENSG00000105705 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1338179947 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_90731,RMVar_hsa_circ_193615,RMVar_hsa_circ_81399,RMVar_hsa_circ_193616 2539 RMVar_ID_2539 Human_SNP_ID_660709730 A-to-I Human chr19 - 19293573 19293573 19293573 TCACTTCTTCTTGTTCTTTTTTTTTTTGAGACAGAGTCTTTCTCTGATGTGCAGGCTGGAGTGGT TCACTTCTTCTTGTTCTTTTTTTTTTTGAGACGGAGTCTTTCTCTGATGTGCAGGCTGGAGTGGT T C SUGP1 Ensembl:ENSG00000105705 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs964719105 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90731,RMVar_hsa_circ_193615,RMVar_hsa_circ_81399,RMVar_hsa_circ_193616 2540 RMVar_ID_2540 Human_SNP_ID_660714268 A-to-I Human chr19 - 19309361 19309361 19309361 TTCCACCTCAGCCTCCCTGTAGCTGGGGCTACAGGGGCATGCCACCACACCTGGCTAATTTTTTT TTCCACCTCAGCCTCCCTGTAGCTGGGGCTACGGGGGCATGCCACCACACCTGGCTAATTTTTTT T C SUGP1 Ensembl:ENSG00000105705 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1421995163 Functional Loss SNV dbSNP153 33..33 33 - - - 2541 RMVar_ID_2541 Human_SNP_ID_660714269 A-to-I Human chr19 - 19309363 19309363 19309363 CCTTCCACCTCAGCCTCCCTGTAGCTGGGGCTACAGGGGCATGCCACCACACCTGGCTAATTTTT CCTTCCACCTCAGCCTCCCTGTAGCTGGGGCTCCAGGGGCATGCCACCACACCTGGCTAATTTTT T G SUGP1 Ensembl:ENSG00000105705 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1381323067 Functional Loss SNV dbSNP153 33..33 33 - - - 2542 RMVar_ID_2542 Human_SNP_ID_660716058 A-to-I Human chr19 - 19315970 19315970 19315970 AAAATTAGCTGGGCATTGTGGCACGTGCCTGTAGTCCCAGCTGCTCAGGAGGCTGAGGCACGAGA AAAATTAGCTGGGCATTGTGGCACGTGCCTGTCGTCCCAGCTGCTCAGGAGGCTGAGGCACGAGA T G SUGP1 Ensembl:ENSG00000105705 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1297636096 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193622,RMVar_hsa_circ_305513 2543 RMVar_ID_2543 Human_SNP_ID_660718143 A-to-I Human chr19 + 19322127 19322127 19322127 TCAGGCCATTCTCCTGCCTCAGCCTCCTGAGTAGCTGAGACTACAGGCGCCCGCCACCACGCCTG TCAGGCCATTCTCCTGCCTCAGCCTCCTGAGTGGCTGAGACTACAGGCGCCCGCCACCACGCCTG A G MAU2 Ensembl:ENSG00000129933 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1416967298 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193623,RMVar_hsa_circ_111927 2544 RMVar_ID_2544 Human_SNP_ID_660718254 A-to-I Human chr19 + 19322493 19322493 19322493 TACTGACGCGGGCCTGTAGTCCCATCTACTCCAGAGGCTGAGGTGGGAGGATCAGCTAAGCCCCG TACTGACGCGGGCCTGTAGTCCCATCTACTCCGGAGGCTGAGGTGGGAGGATCAGCTAAGCCCCG A G MAU2 Ensembl:ENSG00000129933 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs929063925 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13401586 RMVar_hsa_circ_193623,RMVar_hsa_circ_111927 2545 RMVar_ID_2545 Human_SNP_ID_660719047 A-to-I Human chr19 + 19325549 19325549 19325549 TTACCCAGGCTGGAGTGCAGTGGTGCGATTTCAGCTCACTGCATACTCCACCTCCCGGGTTCAAA TTACCCAGGCTGGAGTGCAGTGGTGCGATTTCTGCTCACTGCATACTCCACCTCCCGGGTTCAAA A T MAU2 Ensembl:ENSG00000129933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs548212354 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13401746 RMVar_hsa_circ_193623,RMVar_hsa_circ_111927 2546 RMVar_ID_2546 Human_SNP_ID_660719075 A-to-I Human chr19 + 19325668 19325668 19325668 TGCCCAGCTAATTTTGTATTTTTAGTAGAAACAAGGTTTCATCATGTTAGTCAAGCTGGTCTCGA TGCCCAGCTAATTTTGTATTTTTAGTAGAAACCAGGTTTCATCATGTTAGTCAAGCTGGTCTCGA A C MAU2 Ensembl:ENSG00000129933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs761308405 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13401750 RMVar_hsa_circ_193623,RMVar_hsa_circ_111927 2547 RMVar_ID_2547 Human_SNP_ID_660719922 A-to-I Human chr19 + 19328085 19328085 19328085 GGGAAGCTGAGGCGTGAGGATCACTTGAGCCCAGGAGGTCGAGGCATCAGTGAGCCGTGTTCCTG GGGAAGCTGAGGCGTGAGGATCACTTGAGCCCGGGAGGTCGAGGCATCAGTGAGCCGTGTTCCTG A G MAU2 Ensembl:ENSG00000129933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941571245 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193623,RMVar_hsa_circ_111927 2548 RMVar_ID_2548 Human_SNP_ID_660720451 A-to-I Human chr19 + 19330079 19330078 19330080 TTAGCTCCCTGCCACTTCTGCCTCCTGGGCTCATGTGGTTCTTTTGCCTCAGCTTCCAGAGTAGC TTAGCTCCCTGCCACTTCTGCCTCCTGGGCTC__GTGGTTCTTTTGCCTCAGCTTCCAGAGTAGC CAT C MAU2 Ensembl:ENSG00000129933 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1375923180 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_193623,RMVar_hsa_circ_111927 2549 RMVar_ID_2549 Human_SNP_ID_660720468 A-to-I Human chr19 + 19330156 19330156 19330156 CACACACCACCATGCCCAGCTAATTTTTGTATATTTTGTAGAGATGGGGTTTTGCCATGTTGCCC CACACACCACCATGCCCAGCTAATTTTTGTATGTTTTGTAGAGATGGGGTTTTGCCATGTTGCCC A G MAU2 Ensembl:ENSG00000129933 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1321011235 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193623,RMVar_hsa_circ_111927 2550 RMVar_ID_2550 Human_SNP_ID_660720493 A-to-I Human chr19 + 19330248 19330248 19330248 GCAGTCCACCTGTCTTGGCCTCCCAAAGTGCCAGGATTACAGGCGTGAGCCATTGCTCCCAGCCA GCAGTCCACCTGTCTTGGCCTCCCAAAGTGCCGGGATTACAGGCGTGAGCCATTGCTCCCAGCCA A G MAU2 Ensembl:ENSG00000129933 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1220354788 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193623,RMVar_hsa_circ_111927 2551 RMVar_ID_2551 Human_SNP_ID_660720611 A-to-I Human chr19 + 19330689 19330689 19330689 TTGAACCCGGGAGCCGGAGGGTGCCATGAGCCAAGATCACACCATTGCACTCCAGCCTGGGCAGC TTGAACCCGGGAGCCGGAGGGTGCCATGAGCCGAGATCACACCATTGCACTCCAGCCTGGGCAGC A G MAU2 Ensembl:ENSG00000129933 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1009467387 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193623,RMVar_hsa_circ_111927 2552 RMVar_ID_2552 Human_SNP_ID_660720612 A-to-I Human chr19 + 19330697 19330697 19330697 GGGAGCCGGAGGGTGCCATGAGCCAAGATCACACCATTGCACTCCAGCCTGGGCAGCAAGAGCGA GGGAGCCGGAGGGTGCCATGAGCCAAGATCACCCCATTGCACTCCAGCCTGGGCAGCAAGAGCGA A C MAU2 Ensembl:ENSG00000129933 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs945753000 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193623,RMVar_hsa_circ_111927 2553 RMVar_ID_2553 Human_SNP_ID_660720760 A-to-I Human chr19 + 19331311 19331311 19331311 AACAAGGTCAGGAGACCGAGACCGTCCTGGCTAACATGGTGAAACCCGATTTCTACTGAAAATAC AACAAGGTCAGGAGACCGAGACCGTCCTGGCTGACATGGTGAAACCCGATTTCTACTGAAAATAC A G MAU2 Ensembl:ENSG00000129933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1568652130 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25390212 RMVar_hsa_circ_193623,RMVar_hsa_circ_111927 2554 RMVar_ID_2554 Human_SNP_ID_660720781 A-to-I Human chr19 + 19331395 19331395 19331395 GTGGTGGCGGGCGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATGGCGTGAACCTG GTGGTGGCGGGCGCCTGTAGTCCCAGCTACTCTGGAGGCTGAGGCAGGAGAATGGCGTGAACCTG A T MAU2 Ensembl:ENSG00000129933 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1466637871 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193623,RMVar_hsa_circ_111927 2555 RMVar_ID_2555 Human_SNP_ID_660721000 A-to-I Human chr19 + 19332224 19332224 19332224 GCCCTGTTGCCCAGGCTGGAGTGCAACAGCACAATCATAGCTCACTGCAGCCCCAAACTCCTGGG GCCCTGTTGCCCAGGCTGGAGTGCAACAGCACGATCATAGCTCACTGCAGCCCCAAACTCCTGGG A G MAU2 Ensembl:ENSG00000129933 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1557723 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193623,RMVar_hsa_circ_111927 2556 RMVar_ID_2556 Human_SNP_ID_660721334 A-to-I Human chr19 + 19333329 19333329 19333329 CGGCGTAGCCAGACCCCATCTCTACAAAAAATAAAAAAAATTAGCCAGACGTGGTGGTTCGCACC CGGCGTAGCCAGACCCCATCTCTACAAAAAATTAAAAAAATTAGCCAGACGTGGTGGTTCGCACC A T MAU2 Ensembl:ENSG00000129933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1207146659 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193623,RMVar_hsa_circ_111927 2557 RMVar_ID_2557 Human_SNP_ID_660726264 A-to-I Human chr19 + 19350113 19350113 19350113 GGTCAGGAGTTCAAGACCAGCCTAGCCAACATAGTGAAACCCTGTCTCTTACTAAAAATACAAAA GGTCAGGAGTTCAAGACCAGCCTAGCCAACATGGTGAAACCCTGTCTCTTACTAAAAATACAAAA A G MAU2 Ensembl:ENSG00000129933 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1432603648 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13402224 RMVar_hsa_circ_4883,RMVar_hsa_circ_193629,RMVar_hsa_circ_371806,RMVar_hsa_circ_25620 2558 RMVar_ID_2558 Human_SNP_ID_660726398 A-to-I Human chr19 + 19350550 19350550 19350550 TGCTTGAACCCAGGAGGCAGAGAGGTTGCAGTAAGCCGAGGTCGTGTCATTGTACTCCATCCAGC TGCTTGAACCCAGGAGGCAGAGAGGTTGCAGTGAGCCGAGGTCGTGTCATTGTACTCCATCCAGC A G MAU2 Ensembl:ENSG00000129933 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1316159823 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13402225 RMVar_hsa_circ_4883,RMVar_hsa_circ_193629,RMVar_hsa_circ_371806,RMVar_hsa_circ_25620 2559 RMVar_ID_2559 Human_SNP_ID_660739165 A-to-I Human chr19 + 19398283 19398283 19398283 TGGAGTGCAGTGGTGTGATCTCGGGTCACCGCAACCTCCGCCTCCCGGGTTCAAGCAATTCTCCT TGGAGTGCAGTGGTGTGATCTCGGGTCACCGCCACCTCCGCCTCCCGGGTTCAAGCAATTCTCCT A C GATAD2A Ensembl:ENSG00000167491 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1387385803 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111018,RMVar_hsa_circ_193633 2560 RMVar_ID_2560 Human_SNP_ID_660746847 A-to-I Human chr19 + 19424988 19424988 19424988 ATAAAAAAGGTGTGGTGCAGTCATTGACACCTATAATCCCAGCCCTTTTGGAGGCCAAAGTAGGA ATAAAAAAGGTGTGGTGCAGTCATTGACACCTGTAATCCCAGCCCTTTTGGAGGCCAAAGTAGGA A G GATAD2A Ensembl:ENSG00000167491 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946980393 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111018,RMVar_hsa_circ_193633 2561 RMVar_ID_2561 Human_SNP_ID_660750832 A-to-I Human chr19 + 19439803 19439803 19439803 CCAGGAGGCGGAGGTTGCAGTGAGCCAAGATCACGCCACTGCACTCCAGCATGGGTGACAAAGTG CCAGGAGGCGGAGGTTGCAGTGAGCCAAGATCCCGCCACTGCACTCCAGCATGGGTGACAAAGTG A C GATAD2A Ensembl:ENSG00000167491 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1411336112 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111018,RMVar_hsa_circ_193633,RMVar_hsa_circ_284516 2562 RMVar_ID_2562 Human_SNP_ID_660751708 A-to-I Human chr19 + 19442364 19442364 19442364 AAATCCAAGGCTGGCTGGATGCCGTGGCTCACACCTGTAATCCCAGCACTTCGGGAGGCTGAGGC AAATCCAAGGCTGGCTGGATGCCGTGGCTCACCCCTGTAATCCCAGCACTTCGGGAGGCTGAGGC A C GATAD2A Ensembl:ENSG00000167491 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025107598 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111018,RMVar_hsa_circ_193633,RMVar_hsa_circ_284516 2563 RMVar_ID_2563 Human_SNP_ID_660751709 A-to-I Human chr19 + 19442364 19442364 19442364 AAATCCAAGGCTGGCTGGATGCCGTGGCTCACACCTGTAATCCCAGCACTTCGGGAGGCTGAGGC AAATCCAAGGCTGGCTGGATGCCGTGGCTCACGCCTGTAATCCCAGCACTTCGGGAGGCTGAGGC A G GATAD2A Ensembl:ENSG00000167491 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025107598 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111018,RMVar_hsa_circ_193633,RMVar_hsa_circ_284516 2564 RMVar_ID_2564 Human_SNP_ID_660759671 A-to-I Human chr19 + 19471145 19471145 19471145 TGGTGTGGTGGCGTGCACCTGTAGTCCCAGCTACGTGGGAGGCTGAGGAGGGAGAATTGTTTGAA TGGTGTGGTGGCGTGCACCTGTAGTCCCAGCTTCGTGGGAGGCTGAGGAGGGAGAATTGTTTGAA A T GATAD2A Ensembl:ENSG00000167491 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs530179784 Functional Loss SNV dbSNP153 33..33 33 - - - 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 2565 RMVar_ID_2565 Human_SNP_ID_660762412 A-to-I Human chr19 + 19481381 19481381 19481381 AAGACAGGGTCTTGCTCTGTCTCCCAAACTGGAATGCAGTGGTACAGTCATAGCTCACTGTAGCC AAGACAGGGTCTTGCTCTGTCTCCCAAACTGGTATGCAGTGGTACAGTCATAGCTCACTGTAGCC A T GATAD2A Ensembl:ENSG00000167491 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs908774451 Functional Loss SNV dbSNP153 33..33 33 - - - 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 2566 RMVar_ID_2566 Human_SNP_ID_660772049 A-to-I Human chr19 - 19513619 19513619 19513619 GGAGTGCAGTGGCACGATCTCGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGCGATTCTCCCG GGAGTGCAGTGGCACGATCTCGGCTCACTGCAGCCTCCGCCTCCCGGGTTCAAGCGATTCTCCCG T C TSSK6 Ensembl:ENSG00000178093 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1478380028 Functional Loss SNV dbSNP153 33..33 33 - - - 2567 RMVar_ID_2567 Human_SNP_ID_660774730 A-to-I Human chr19 + 19522031 19522031 19522031 AGTTTTTAATTTCAATAAAGTCCGGGCTGGGCACGGTGGCTCATGCCTGTAATTCCAGCACTTTG AGTTTTTAATTTCAATAAAGTCCGGGCTGGGCGCGGTGGCTCATGCCTGTAATTCCAGCACTTTG A G NDUFA13,AC011448.1 Ensembl:ENSG00000186010,Ensembl:ENSG00000258674 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1410359511 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193646,RMVar_hsa_circ_85005,RMVar_hsa_circ_101918,RMVar_hsa_circ_193647 2568 RMVar_ID_2568 Human_SNP_ID_660774950 A-to-I Human chr19 + 19522746 19522746 19522746 GTGATCCGCCTGCCTTGGCCTCCCAAAGTGCTAGAATTACAGGCGTGAGCCACTGCGCCCGGCAG GTGATCCGCCTGCCTTGGCCTCCCAAAGTGCTGGAATTACAGGCGTGAGCCACTGCGCCCGGCAG A G NDUFA13,AC011448.1 Ensembl:ENSG00000186010,Ensembl:ENSG00000258674 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs558540963 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193646,RMVar_hsa_circ_85005,RMVar_hsa_circ_101918,RMVar_hsa_circ_193647 2569 RMVar_ID_2569 Human_SNP_ID_660775229 A-to-I Human chr19 + 19523998 19523998 19523998 CACTGTGTTGCACAGGCTAGTTGCAAACTCCTAGTCAAGTGATCCTCTCACCTCAGCCTCCCAAA CACTGTGTTGCACAGGCTAGTTGCAAACTCCTGGTCAAGTGATCCTCTCACCTCAGCCTCCCAAA A G NDUFA13,AC011448.1 Ensembl:ENSG00000186010,Ensembl:ENSG00000258674 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1329230334 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193646,RMVar_hsa_circ_85005,RMVar_hsa_circ_101918,RMVar_hsa_circ_193647 2570 RMVar_ID_2570 Human_SNP_ID_660791381 A-to-I Human chr19 - 19577807 19577807 19577807 GTCGCCAGGCTGGAGTGCACTGGCGCGATCTCAGCTCACTGCAACCTCTGCCTCACAGTTCCAAG GTCGCCAGGCTGGAGTGCACTGGCGCGATCTCGGCTCACTGCAACCTCTGCCTCACAGTTCCAAG T C PBX4 Ensembl:ENSG00000105717 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1257120511 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_294980,RMVar_hsa_circ_193656,RMVar_hsa_circ_25911 2571 RMVar_ID_2571 Human_SNP_ID_660794153 A-to-I Human chr19 - 19589264 19589264 19589264 ACCACCACACTCCTCTAATTTTTTGTATTTTTAGTAGAGATGGGGTTTCATCGTGTTAGCCAGGA ACCACCACACTCCTCTAATTTTTTGTATTTTTCGTAGAGATGGGGTTTCATCGTGTTAGCCAGGA T G PBX4 Ensembl:ENSG00000105717 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs571341995 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_294980,RMVar_hsa_circ_193656,RMVar_hsa_circ_25911,RMVar_hsa_circ_193658 2572 RMVar_ID_2572 Human_SNP_ID_660805049 A-to-I Human chr19 - 19632524 19632524 19632524 GTTGGAATCTTTTATTTTTTTTTGGAGACAGAATCTCACTGTGTTGCCCAACTGGAGTGCAGTGG GTTGGAATCTTTTATTTTTTTTTGGAGACAGAGTCTCACTGTGTTGCCCAACTGGAGTGCAGTGG T C GMIP Ensembl:ENSG00000089639 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1447168206 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103925,RMVar_hsa_circ_115029,RMVar_hsa_circ_193660,RMVar_hsa_circ_193661 2573 RMVar_ID_2573 Human_SNP_ID_660805198 A-to-I Human chr19 - 19633183 19633183 19633183 GTGGTGGTGTGTACCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAGCCCA GTGGTGGTGTGTACCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAGCCCA T C GMIP Ensembl:ENSG00000089639 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs970553086 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103925,RMVar_hsa_circ_115029,RMVar_hsa_circ_193660,RMVar_hsa_circ_193661 2574 RMVar_ID_2574 Human_SNP_ID_660805219 A-to-I Human chr19 - 19633270 19633270 19633270 GCAAATCACCTGAGGTCAGGAGTTCGAGACTAATCCAACCAATAAGGAGAAACCTGTCTCTACTA GCAAATCACCTGAGGTCAGGAGTTCGAGACTAGTCCAACCAATAAGGAGAAACCTGTCTCTACTA T C GMIP Ensembl:ENSG00000089639 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11878202 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103925,RMVar_hsa_circ_115029,RMVar_hsa_circ_193660,RMVar_hsa_circ_193661 2575 RMVar_ID_2575 Human_SNP_ID_660807784 A-to-I Human chr19 - 19641219 19641219 19641219 AAATTTAGCCGGGCGCAGTGGCGAGTGCCTGTAGTCCCAGATACTCGGGAGGCTGAGGCAGGAGA AAATTTAGCCGGGCGCAGTGGCGAGTGCCTGTGGTCCCAGATACTCGGGAGGCTGAGGCAGGAGA T C GMIP Ensembl:ENSG00000089639 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928190741 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103925,RMVar_hsa_circ_193661,RMVar_hsa_circ_125929,RMVar_hsa_circ_193662,RMVar_hsa_circ_127868,RMVar_hsa_circ_193666 2576 RMVar_ID_2576 Human_SNP_ID_660814124 A-to-I Human chr19 - 19659745 19659745 19659745 TGAGGTGCTGTCCTTCGAATTCCAGAAGATCAAGTATTCCTACGATGCCCTGGAGAAGAAGCAGT TGAGGTGCTGTCCTTCGAATTCCAGAAGATCAGGTATTCCTACGATGCCCTGGAGAAGAAGCAGT T C ATP13A1 Ensembl:ENSG00000105726 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1380287466 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_53470,Human_RBP_ID_1881448,Human_RBP_ID_9380854,Human_RBP_ID_18725156,Human_RBP_ID_18997383 Human_Splice_Rec_1983838,Human_Splice_Rec_1983888,Human_Splice_Rec_1984058 Human_miRNA_ID_2696253 RMVar_hsa_circ_193675,RMVar_hsa_circ_101579,RMVar_hsa_circ_377481,RMVar_hsa_circ_19760,RMVar_hsa_circ_371468,RMVar_hsa_circ_193684 2577 RMVar_ID_2577 Human_SNP_ID_660816724 A-to-I Human chr19 + 19667352 19667352 19667352 AAAAAAAAAAAAAATTGGCCGGGCATGGTGGCACATGCCTGTAGTTCCAGCTACTCGGACTCGGG AAAAAAAAAAAAAATTGGCCGGGCATGGTGGCTCATGCCTGTAGTTCCAGCTACTCGGACTCGGG A T lnc-ZNF101-1 RNACentral:URS0000D5E368 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs987212433 Functional Loss SNV dbSNP153 33..33 33 - - - 2578 RMVar_ID_2578 Human_SNP_ID_660817424 A-to-I Human chr19 + 19669525 19669521 19669525 CATTATTTCTATTATTTTTGAGACGGAGTCTCACTCTGTCGCCCAGGCTGGAGTGCAGTGGCACT CATTATTTCTATTATTTTTGAGACGGAGT____CTCTGTCGCCCAGGCTGGAGTGCAGTGGCACT TCTCA T ZNF101 Ensembl:ENSG00000181896 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1016967291 Functional Loss DEL dbSNP153 30..33 33 - - - 2579 RMVar_ID_2579 Human_SNP_ID_660817425 A-to-I Human chr19 + 19669525 19669525 19669525 CATTATTTCTATTATTTTTGAGACGGAGTCTCACTCTGTCGCCCAGGCTGGAGTGCAGTGGCACT CATTATTTCTATTATTTTTGAGACGGAGTCTCTCTCTGTCGCCCAGGCTGGAGTGCAGTGGCACT A T ZNF101 Ensembl:ENSG00000181896 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1233489770 Functional Loss SNV dbSNP153 33..33 33 - - - 2580 RMVar_ID_2580 Human_SNP_ID_660817627 A-to-I Human chr19 + 19670406 19670402 19670406 GCTGGGACCACAGGCATGCGCCACGCCCGGCTAGTTTTTATTTTTTGTAGAGACAAGGTCTCACT GCTGGGACCACAGGCATGCGCCACGCCCG____GTTTTTATTTTTTGTAGAGACAAGGTCTCACT GGCTA G ZNF101 Ensembl:ENSG00000181896 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1220248652 Functional Loss DEL dbSNP153 30..33 33 - - - 2581 RMVar_ID_2581 Human_SNP_ID_660817628 A-to-I Human chr19 + 19670406 19670406 19670406 GCTGGGACCACAGGCATGCGCCACGCCCGGCTAGTTTTTATTTTTTGTAGAGACAAGGTCTCACT GCTGGGACCACAGGCATGCGCCACGCCCGGCTGGTTTTTATTTTTTGTAGAGACAAGGTCTCACT A G ZNF101 Ensembl:ENSG00000181896 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1280142767 Functional Loss SNV dbSNP153 33..33 33 - - - 2582 RMVar_ID_2582 Human_SNP_ID_660817634 A-to-I Human chr19 + 19670422 19670422 19670422 TGCGCCACGCCCGGCTAGTTTTTATTTTTTGTAGAGACAAGGTCTCACTATGTTGCCCAGTCTGC TGCGCCACGCCCGGCTAGTTTTTATTTTTTGTGGAGACAAGGTCTCACTATGTTGCCCAGTCTGC A G ZNF101 Ensembl:ENSG00000181896 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1306887725 Functional Loss SNV dbSNP153 33..33 33 - - - 2583 RMVar_ID_2583 Human_SNP_ID_660818742 A-to-I Human chr19 + 19674316 19674316 19674316 CTCCTGCCTTAGCCTCTCGAGTAGCTGGGACTACAGGTGTGGGCTACCACACCTGGCTGATTGTG CTCCTGCCTTAGCCTCTCGAGTAGCTGGGACTGCAGGTGTGGGCTACCACACCTGGCTGATTGTG A G ZNF101 Ensembl:ENSG00000181896 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982343017 Functional Loss SNV dbSNP153 33..33 33 - - - 2584 RMVar_ID_2584 Human_SNP_ID_660820349 A-to-I Human chr19 + 19680361 19680361 19680361 CATATCGGCTGGGTACGGTGGCTCACGCTTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGTGG CATATCGGCTGGGTACGGTGGCTCACGCTTGTGATCCCAGCACTTTGGGAGGCTGAGGCGGGTGG A G ZNF101 Ensembl:ENSG00000181896 Protein coding 3'UTR GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs1187145677 Functional Loss SNV dbSNP153 33..33 33 - - - 2585 RMVar_ID_2585 Human_SNP_ID_660820437 A-to-I Human chr19 + 19680683 19680682 19680684 GTGGCTCATGCCTGTAAAACCAGCACTTTGGGAAGCCGAGGTGGGTGGATCACGAGGTCCAGAGA GTGGCTCATGCCTGTAAAACCAGCACTTTGGG__GCCGAGGTGGGTGGATCACGAGGTCCAGAGA GAA G ZNF101 Ensembl:ENSG00000181896 Protein coding intron GSE38233;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,32596459 RNA-Seq:(High) rs1197150777 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_6728299 2586 RMVar_ID_2586 Human_SNP_ID_660820449 A-to-I Human chr19 + 19680702 19680702 19680702 CCAGCACTTTGGGAAGCCGAGGTGGGTGGATCACGAGGTCCAGAGATGGAGACTATCTTGGCCAA CCAGCACTTTGGGAAGCCGAGGTGGGTGGATCGCGAGGTCCAGAGATGGAGACTATCTTGGCCAA A G ZNF101 Ensembl:ENSG00000181896 Protein coding intron GSE38233;GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,32596459 RNA-Seq:(High) rs1275522986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22232240 2587 RMVar_ID_2587 Human_SNP_ID_660820478 A-to-I Human chr19 + 19680809 19680809 19680809 AGGCGTGGTGGTGTGTGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCTTGAA AGGCGTGGTGGTGTGTGCCTGTAGTCCCAGCTTCTCGGGAGGCTGAGGCAGGAGAATTGCTTGAA A T ZNF101 Ensembl:ENSG00000181896 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1230102708 Functional Loss SNV dbSNP153 33..33 33 - - - 2588 RMVar_ID_2588 Human_SNP_ID_660820505 A-to-I Human chr19 + 19680901 19680901 19680901 GAGATCGCGCCGCTGCACTCCAGCCTGGTGACAGAGCGAGACTTCGTCTCAAAACAAACAAAAAA GAGATCGCGCCGCTGCACTCCAGCCTGGTGACGGAGCGAGACTTCGTCTCAAAACAAACAAAAAA A G ZNF101 Ensembl:ENSG00000181896 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs959689859 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1984078 2589 RMVar_ID_2589 Human_SNP_ID_660820662 A-to-I Human chr19 + 19681526 19681526 19681526 TAATCCCAGCATTTTGGGAGGCTGGGGTGGGTAGATTGCTTGAGGCCAGGTATTCAAGACCAGCC TAATCCCAGCATTTTGGGAGGCTGGGGTGGGTGGATTGCTTGAGGCCAGGTATTCAAGACCAGCC A G ZNF101 Ensembl:ENSG00000181896 Protein coding 3'UTR GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,29796672,31158229 RNA-Seq:(High) rs890585500 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26473862 2590 RMVar_ID_2590 Human_SNP_ID_660820686 A-to-I Human chr19 + 19681643 19681643 19681643 ATGATGGTGTTCGCCTGTAGTCCCAGCTACTCAGGAAGCTGAGGTGGGAGGATTGCTTGAGTTTG ATGATGGTGTTCGCCTGTAGTCCCAGCTACTCGGGAAGCTGAGGTGGGAGGATTGCTTGAGTTTG A G ZNF101 Ensembl:ENSG00000181896 Protein coding 3'UTR GSE38233;GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,32596459 RNA-Seq:(High) rs548030250 Functional Loss SNV dbSNP153 33..33 33 - - - 2591 RMVar_ID_2591 Human_SNP_ID_660820894 A-to-I Human chr19 + 19682299 19682299 19682299 TAGAGTGCAGTGGCGCGATCTTGACTCACTGTAACCTCTGACTTCTGGGTTCAAGCAATTCTCCT TAGAGTGCAGTGGCGCGATCTTGACTCACTGTGACCTCTGACTTCTGGGTTCAAGCAATTCTCCT A G ZNF101 Ensembl:ENSG00000181896 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1018746567 Functional Loss SNV dbSNP153 33..33 33 - - - 2592 RMVar_ID_2592 Human_SNP_ID_660820908 A-to-I Human chr19 + 19682361 19682361 19682361 CCTGCTTCAGTCTCCGAAGCATCTGGGATTACAGGCGCACGCCACCATGCCCAGCTAAATTTTTG CCTGCTTCAGTCTCCGAAGCATCTGGGATTACGGGCGCACGCCACCATGCCCAGCTAAATTTTTG A G ZNF101 Ensembl:ENSG00000181896 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs968131524 Functional Loss SNV dbSNP153 33..33 33 - - - 2593 RMVar_ID_2593 Human_SNP_ID_660820942 A-to-I Human chr19 + 19682482 19682482 19682482 ACCTCAAGGAATCCATCCTCTTCAGCCTCGCAAAGTGCTGAGATTATAGGCATGAGACACCTTGC ACCTCAAGGAATCCATCCTCTTCAGCCTCGCAGAGTGCTGAGATTATAGGCATGAGACACCTTGC A G ZNF101 Ensembl:ENSG00000181896 Protein coding 3'UTR GSE123020:GSM3490829,GSM3490830,GSM3490831 esophageal squamous carcinoma cells,EC109 cell line - 32596459 RNA-Seq:(High) rs1008597073 Functional Loss SNV dbSNP153 33..33 33 - - - 2594 RMVar_ID_2594 Human_SNP_ID_660821017 A-to-I Human chr19 + 19682840 19682840 19682840 AGTCTATTTTTGTTTGTTTTCTTTTGTTTTTGAGACTGAGTCTTGCTCTGTCGCCAGGCTGAAGT AGTCTATTTTTGTTTGTTTTCTTTTGTTTTTGTGACTGAGTCTTGCTCTGTCGCCAGGCTGAAGT A T ZNF101 Ensembl:ENSG00000181896 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs76153775 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6728322 2595 RMVar_ID_2595 Human_SNP_ID_660821082 A-to-I Human chr19 + 19683065 19683065 19683065 TGACCTTGTGATCCACCCCACCTTGGCCTCCCAAAGTGCTGAGATTACAGGAGTGAGCCACTGCG TGACCTTGTGATCCACCCCACCTTGGCCTCCCGAAGTGCTGAGATTACAGGAGTGAGCCACTGCG A G ZNF101 Ensembl:ENSG00000181896 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,31158229,32596459 RNA-Seq:(High) rs1309202688 Functional Loss SNV dbSNP153 33..33 33 - - - 2596 RMVar_ID_2596 Human_SNP_ID_660821083 A-to-I Human chr19 + 19683066 19683066 19683066 GACCTTGTGATCCACCCCACCTTGGCCTCCCAAAGTGCTGAGATTACAGGAGTGAGCCACTGCGA GACCTTGTGATCCACCCCACCTTGGCCTCCCACAGTGCTGAGATTACAGGAGTGAGCCACTGCGA A C ZNF101 Ensembl:ENSG00000181896 Protein coding 3'UTR GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,29796672,31158229,31158229 RNA-Seq:(High) rs943027615 Functional Loss SNV dbSNP153 33..33 33 - - - 2597 RMVar_ID_2597 Human_SNP_ID_660824746 A-to-I Human chr19 + 19691840 19691840 19691840 TCGGCTCACTGCAACCTCTGACCCCCAAGTTCAAGTGATTCTCGTGCCTCAGCCTCCTGTAATCT TCGGCTCACTGCAACCTCTGACCCCCAAGTTCGAGTGATTCTCGTGCCTCAGCCTCCTGTAATCT A G lnc-ZNF101-1 RNACentral:URS0000D5E368 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs962799637 Functional Loss SNV dbSNP153 33..33 33 - - - 2598 RMVar_ID_2598 Human_SNP_ID_660833847 A-to-I Human chr19 - 19729456 19729456 19729456 AAAAAATTAGCTGGATGTGGGGGCTGGCGCCTATAATTCCAGCTACTCGGGAGGCTGAGGCAGGA AAAAAATTAGCTGGATGTGGGGGCTGGCGCCTGTAATTCCAGCTACTCGGGAGGCTGAGGCAGGA T C ZNF14 Ensembl:ENSG00000105708 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs529609142 Functional Loss SNV dbSNP153 33..33 33 - - - 2599 RMVar_ID_2599 Human_SNP_ID_660834006 A-to-I Human chr19 - 19730231 19730231 19730231 CCTGAGGTAAGGAGTTCAAGACCACCCTGACCAACATAGTGAAATCCATCTCTACTAAAAATACA CCTGAGGTAAGGAGTTCAAGACCACCCTGACCGACATAGTGAAATCCATCTCTACTAAAAATACA T C ZNF14 Ensembl:ENSG00000105708 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1447612357 Functional Loss SNV dbSNP153 33..33 33 - - - 2600 RMVar_ID_2600 Human_SNP_ID_660841195 A-to-I Human chr19 - 19756677 19756677 19756677 CCCGTCTCTACTAAAAATACAAAAAATTAGCCAGGCACGGTGGCGGGCGCCTGTAGTCCCAGCTA CCCGTCTCTACTAAAAATACAAAAAATTAGCCGGGCACGGTGGCGGGCGCCTGTAGTCCCAGCTA T C LINC00663 RNACentral:URS000075C943 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs573533970 Functional Loss SNV dbSNP153 33..33 33 - - - 2601 RMVar_ID_2601 Human_SNP_ID_660841335 A-to-I Human chr19 - 19757231 19757231 19757231 GCCTCCATCACCATGCCTGGCTAATTTTTTGTATTTTTGTAGAGATGAGGTTTCACCTTGTTGGC GCCTCCATCACCATGCCTGGCTAATTTTTTGTGTTTTTGTAGAGATGAGGTTTCACCTTGTTGGC T C LINC00663 RNACentral:URS000075C943 lincRNA intron GSE47997;GSE107867 K562 cells&HepG2 cells;ASD brains,Fragile X samples from NIH NeuroBioBank - 23474544,30559470 RNA-Seq:(High) rs1423881963 Functional Loss SNV dbSNP153 33..33 33 - - - 2602 RMVar_ID_2602 Human_SNP_ID_660841336 A-to-I Human chr19 - 19757241 19757241 19757241 GGGACTACAGGCCTCCATCACCATGCCTGGCTAATTTTTTGTATTTTTGTAGAGATGAGGTTTCA GGGACTACAGGCCTCCATCACCATGCCTGGCTGATTTTTTGTATTTTTGTAGAGATGAGGTTTCA T C LINC00663 RNACentral:URS000075C943 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs760374639 Functional Loss SNV dbSNP153 33..33 33 - - - 2603 RMVar_ID_2603 Human_SNP_ID_660841340 A-to-I Human chr19 - 19757270 19757270 19757270 ATTCCCCTGCCTCAGCCTCCCCAGTAGCTGGGACTACAGGCCTCCATCACCATGCCTGGCTAATT ATTCCCCTGCCTCAGCCTCCCCAGTAGCTGGGGCTACAGGCCTCCATCACCATGCCTGGCTAATT T C LINC00663 RNACentral:URS000075C943 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs575794033 Functional Loss SNV dbSNP153 33..33 33 - - - 2604 RMVar_ID_2604 Human_SNP_ID_660841341 A-to-I Human chr19 - 19757277 19757277 19757277 TCAGATGATTCCCCTGCCTCAGCCTCCCCAGTAGCTGGGACTACAGGCCTCCATCACCATGCCTG TCAGATGATTCCCCTGCCTCAGCCTCCCCAGTTGCTGGGACTACAGGCCTCCATCACCATGCCTG T A LINC00663 RNACentral:URS000075C943 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs993329266 Functional Loss SNV dbSNP153 33..33 33 - - - 2605 RMVar_ID_2605 Human_SNP_ID_660848797 A-to-I Human chr19 - 19786319 19786319 19786319 ACAATCTCGGCTCACTGCAACCTCCGCCTCCCAGGTTCAAGTGATTCTTCTGCCTCAGCCTCTCA ACAATCTCGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGTGATTCTTCTGCCTCAGCCTCTCA T C AC011477.3,ZNF506 Ensembl:ENSG00000267581,Ensembl:ENSG00000081665 lincRNA,Protein coding intron,3'UTR GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs916795183 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114335,RMVar_hsa_circ_193689,RMVar_hsa_circ_90759,RMVar_hsa_circ_193688 2606 RMVar_ID_2606 Human_SNP_ID_660848807 A-to-I Human chr19 - 19786348 19786348 19786348 ACTTGTTGCCCAGGCTGGAGTGCAATGGTACAATCTCGGCTCACTGCAACCTCCGCCTCCCAGGT ACTTGTTGCCCAGGCTGGAGTGCAATGGTACAGTCTCGGCTCACTGCAACCTCCGCCTCCCAGGT T C AC011477.3,ZNF506 Ensembl:ENSG00000267581,Ensembl:ENSG00000081665 lincRNA,Protein coding intron,3'UTR GSE38233;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;Bronchiolar epithelium,BERP35T4 cell line - 24183664,31158229 RNA-Seq:(High) rs1294892411 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114335,RMVar_hsa_circ_193689,RMVar_hsa_circ_90759,RMVar_hsa_circ_193688 2607 RMVar_ID_2607 Human_SNP_ID_660848809 A-to-I Human chr19 + 19786352 19786352 19786352 GGGAGGCGGAGGTTGCAGTGAGCCGAGATTGTACCATTGCACTCCAGCCTGGGCAACAAGTGCGA GGGAGGCGGAGGTTGCAGTGAGCCGAGATTGTGCCATTGCACTCCAGCCTGGGCAACAAGTGCGA A G ZNF56 Ensembl:ENSG00000267419 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1381898929 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17388223 2608 RMVar_ID_2608 Human_SNP_ID_660848927 A-to-I Human chr19 - 19786831 19786831 19786831 ATGGAACAGGCCAGGCACGGTGGCTCATGCCTATAATTCCAGCACTTTGGAGGGCCAAGGCAGGC ATGGAACAGGCCAGGCACGGTGGCTCATGCCTCTAATTCCAGCACTTTGGAGGGCCAAGGCAGGC T G AC011477.3,ZNF506 Ensembl:ENSG00000267581,Ensembl:ENSG00000081665 lincRNA,Protein coding intron,3'UTR GSE38233;GSE107867 cultured B-cells;ASD brains,frontal_cortex - 24183664,30559470 RNA-Seq:(High) rs1439134964 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3589450 Human_Splice_Rec_1984184,Human_Splice_Rec_1984194,Human_Splice_Rec_1984200,Human_Splice_Rec_1984210 RMVar_hsa_circ_114335,RMVar_hsa_circ_193689,RMVar_hsa_circ_90759,RMVar_hsa_circ_193688 2609 RMVar_ID_2609 Human_SNP_ID_660849657 A-to-I Human chr19 - 19789691 19789691 19789691 CCGCGCCACTGCACTCCAGCTTGGGTGACAGAATGAGACTCCATCTCAAACAAAACAAAACAAAC CCGCGCCACTGCACTCCAGCTTGGGTGACAGAGTGAGACTCCATCTCAAACAAAACAAAACAAAC T C AC011477.3,ZNF506,AC011477.1 Ensembl:ENSG00000267581,Ensembl:ENSG00000081665,Ensembl:ENSG00000267481 lincRNA,Protein coding,lincRNA intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1381224488 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23310125 RMVar_hsa_circ_114335,RMVar_hsa_circ_193689,RMVar_hsa_circ_90759,RMVar_hsa_circ_193688 2610 RMVar_ID_2610 Human_SNP_ID_660849665 A-to-I Human chr19 - 19789727 19789727 19789727 TTGAACCTGGGAGGCGGAGGTTGCTGTTAGCCAAGACCGCGCCACTGCACTCCAGCTTGGGTGAC TTGAACCTGGGAGGCGGAGGTTGCTGTTAGCCGAGACCGCGCCACTGCACTCCAGCTTGGGTGAC T C AC011477.3,ZNF506,AC011477.1 Ensembl:ENSG00000267581,Ensembl:ENSG00000081665,Ensembl:ENSG00000267481 lincRNA,Protein coding,lincRNA intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs915821819 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114335,RMVar_hsa_circ_193689,RMVar_hsa_circ_90759,RMVar_hsa_circ_193688 2611 RMVar_ID_2611 Human_SNP_ID_660850121 A-to-I Human chr19 + 19791687 19791687 19791687 GAAAGGAGCGCTTCCTCAGACGGGGTTTCACTATGTTGGCCAGGATGGTCTTGAACTCCTGACCT GAAAGGAGCGCTTCCTCAGACGGGGTTTCACTGTGTTGGCCAGGATGGTCTTGAACTCCTGACCT A G ZNF56 Ensembl:ENSG00000267419 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs932711880 Functional Loss SNV dbSNP153 33..33 33 - - - 2612 RMVar_ID_2612 Human_SNP_ID_660850123 A-to-I Human chr19 + 19791696 19791696 19791696 GCTTCCTCAGACGGGGTTTCACTATGTTGGCCAGGATGGTCTTGAACTCCTGACCTCAGACAATC GCTTCCTCAGACGGGGTTTCACTATGTTGGCCGGGATGGTCTTGAACTCCTGACCTCAGACAATC A G ZNF56 Ensembl:ENSG00000267419 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1252393299 Functional Loss SNV dbSNP153 33..33 33 - - - 2613 RMVar_ID_2613 Human_SNP_ID_660850127 A-to-I Human chr19 - 19791706 19791706 19791706 AAGGCAGGTGGATTGTCTGAGGTCAGGAGTTCAAGACCATCCTGGCCAACATAGTGAAACCCCGT AAGGCAGGTGGATTGTCTGAGGTCAGGAGTTCGAGACCATCCTGGCCAACATAGTGAAACCCCGT T C AC011477.3,ZNF506 Ensembl:ENSG00000267581,Ensembl:ENSG00000081665 lincRNA,Protein coding intron,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1189295453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1984208 RMVar_hsa_circ_114335,RMVar_hsa_circ_193689,RMVar_hsa_circ_90759,RMVar_hsa_circ_193688 2614 RMVar_ID_2614 Human_SNP_ID_660850131 A-to-I Human chr19 - 19791714 19791714 19791714 CACTTTCCAAGGCAGGTGGATTGTCTGAGGTCAGGAGTTCAAGACCATCCTGGCCAACATAGTGA CACTTTCCAAGGCAGGTGGATTGTCTGAGGTCTGGAGTTCAAGACCATCCTGGCCAACATAGTGA T A AC011477.3,ZNF506 Ensembl:ENSG00000267581,Ensembl:ENSG00000081665 lincRNA,Protein coding intron,3'UTR GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line - 24183664,31158229 RNA-Seq:(High) rs1367615055 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1984208 RMVar_hsa_circ_114335,RMVar_hsa_circ_193689,RMVar_hsa_circ_90759,RMVar_hsa_circ_193688 2615 RMVar_ID_2615 Human_SNP_ID_660850138 A-to-I Human chr19 - 19791770 19791770 19791770 TACAGAAAAATAAATAAAATATGGCCAGGTGCAGTGGCTCAGGCCTGTAATCCCAGCACTTTCCA TACAGAAAAATAAATAAAATATGGCCAGGTGCGGTGGCTCAGGCCTGTAATCCCAGCACTTTCCA T C AC011477.3,ZNF506 Ensembl:ENSG00000267581,Ensembl:ENSG00000081665 lincRNA,Protein coding intron,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1482749389 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114335,RMVar_hsa_circ_193689,RMVar_hsa_circ_90759,RMVar_hsa_circ_193688 2616 RMVar_ID_2616 Human_SNP_ID_660850266 A-to-I Human chr19 + 19792304 19792304 19792304 AAGGTCAGGAGATTGACCATCCCGGCTAACACAGTGAAACCCCATCTCTACTAAAAATACAAAAA AAGGTCAGGAGATTGACCATCCCGGCTAACACGGTGAAACCCCATCTCTACTAAAAATACAAAAA A G ZNF56 Ensembl:ENSG00000267419 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1220580314 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_139235,Human_RBP_ID_18532710 2617 RMVar_ID_2617 Human_SNP_ID_660851348 A-to-I Human chr19 - 19796124 19796124 19796124 GTATCTGTTACCACACCTGGCTAACGTTTTGTAGTTTTGTAGAGACGGGGTTTCACCATCTTTGC GTATCTGTTACCACACCTGGCTAACGTTTTGTGGTTTTGTAGAGACGGGGTTTCACCATCTTTGC T C AC011477.3,ZNF506 Ensembl:ENSG00000267581,Ensembl:ENSG00000081665 lincRNA,Protein coding intron,intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs769196427 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114335,RMVar_hsa_circ_193689 2618 RMVar_ID_2618 Human_SNP_ID_660851366 A-to-I Human chr19 + 19796213 19796213 19796213 TGAGGGAGGAGAATTGCTTGAACTGTGGAGGCAGAGATTGTAGTGAGCCAAGATCATGCCATTGT TGAGGGAGGAGAATTGCTTGAACTGTGGAGGCCGAGATTGTAGTGAGCCAAGATCATGCCATTGT A C ZNF56 Ensembl:ENSG00000267419 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404590229 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17387822 2619 RMVar_ID_2619 Human_SNP_ID_660851373 A-to-I Human chr19 - 19796242 19796242 19796242 GAGTCTCACTCTGTTACCTAGGCTGGAGTACAATGGCATGATCTTGGCTCACTACAATCTCTGCC GAGTCTCACTCTGTTACCTAGGCTGGAGTACAGTGGCATGATCTTGGCTCACTACAATCTCTGCC T C AC011477.3,ZNF506 Ensembl:ENSG00000267581,Ensembl:ENSG00000081665 lincRNA,Protein coding intron,intron GSE38233;GSE107867 cultured B-cells;ASD brains,temporal_cortex - 24183664,30559470 RNA-Seq:(High) rs1249037177 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6728483 RMVar_hsa_circ_114335,RMVar_hsa_circ_193689 2620 RMVar_ID_2620 Human_SNP_ID_660851376 A-to-I Human chr19 - 19796245 19796245 19796245 ACAGAGTCTCACTCTGTTACCTAGGCTGGAGTACAATGGCATGATCTTGGCTCACTACAATCTCT ACAGAGTCTCACTCTGTTACCTAGGCTGGAGTGCAATGGCATGATCTTGGCTCACTACAATCTCT T C AC011477.3,ZNF506 Ensembl:ENSG00000267581,Ensembl:ENSG00000081665 lincRNA,Protein coding intron,intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1321550286 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6728483 RMVar_hsa_circ_114335,RMVar_hsa_circ_193689 2621 RMVar_ID_2621 Human_SNP_ID_660851461 A-to-I Human chr19 - 19796560 19796560 19796560 TCTCTACTAAAAATACAAAAAATTAGCCGGGCATGGTGGCGGGCACCTGTAGTCCCATCTAGTTG TCTCTACTAAAAATACAAAAAATTAGCCGGGCGTGGTGGCGGGCACCTGTAGTCCCATCTAGTTG T C AC011477.3,ZNF506 Ensembl:ENSG00000267581,Ensembl:ENSG00000081665 lincRNA,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1017147393 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114335,RMVar_hsa_circ_193689 2622 RMVar_ID_2622 Human_SNP_ID_660963641 A-to-I Human chr19 + 20197229 20197229 20197229 TTTCATCAATTTTCAAATTCAAAGAGACATAAAAGAAGACATACTGAAAAAAAACCTTTGAAATA TTTCATCAATTTTCAAATTCAAAGAGACATAAGAGAAGACATACTGAAAAAAAACCTTTGAAATA A G ZNF486 Ensembl:ENSG00000256229 Protein coding CDS GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1555718147 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193697 2623 RMVar_ID_2623 Human_SNP_ID_660982209 A-to-I Human chr19 - 20257758 20257758 20257758 CCTGCATATCCACACTTCACAAACCCAGTGTCATTGTCGCACACCACCACCTTCCTGCTCTGGCT CCTGCATATCCACACTTCACAAACCCAGTGTCGTTGTCGCACACCACCACCTTCCTGCTCTGGCT T C AC011447.3 Ensembl:ENSG00000267383 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1367480140 Functional Loss SNV dbSNP153 33..33 33 - - - 2624 RMVar_ID_2624 Human_SNP_ID_660982225 A-to-I Human chr19 - 20257834 20257834 20257834 AAAAAACAAGGTTGGGCATTACATGATAATAGATCTTCCAACCAAAGCTGGGAAGATGTGTTCTG AAAAAACAAGGTTGGGCATTACATGATAATAGCTCTTCCAACCAAAGCTGGGAAGATGTGTTCTG T G AC011447.3 Ensembl:ENSG00000267383 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1256786601 Functional Loss SNV dbSNP153 33..33 33 - - - 2625 RMVar_ID_2625 Human_SNP_ID_661078835 A-to-I Human chr19 - 20620713 20620713 20620713 CGCCAATGTGGTGAAACCCTGTCTCTACTAAAAATAGAAAAATTAGCCAGTCATGGTGGCGCACA CGCCAATGTGGTGAAACCCTGTCTCTACTAAAGATAGAAAAATTAGCCAGTCATGGTGGCGCACA T C AC010636.2,ZNF626 Ensembl:ENSG00000269110,Ensembl:ENSG00000188171 lincRNA,Protein coding intron,3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1555768587 Functional Loss SNV dbSNP153 33..33 33 - - - 2626 RMVar_ID_2626 Human_SNP_ID_661079168 A-to-I Human chr19 - 20621990 20621990 20621990 TAGACATGGGGTTTCCCCATATTGGTCAGGCTAGTCTCAAACTCCTGAGCTCAAGCGATCCACCC TAGACATGGGGTTTCCCCATATTGGTCAGGCTCGTCTCAAACTCCTGAGCTCAAGCGATCCACCC T G AC010636.2,ZNF626 Ensembl:ENSG00000269110,Ensembl:ENSG00000188171 lincRNA,Protein coding intron,3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1455531236 Functional Loss SNV dbSNP153 33..33 33 - - - 2627 RMVar_ID_2627 Human_SNP_ID_661079197 A-to-I Human chr19 - 20622104 20622104 20622104 ACAATGACTGCAACCTCCACCTCCCAAGTTCAAGAAATTCTCCTGCCTCAGCCTCCCGAGTAGTG ACAATGACTGCAACCTCCACCTCCCAAGTTCAGGAAATTCTCCTGCCTCAGCCTCCCGAGTAGTG T C AC010636.2,ZNF626 Ensembl:ENSG00000269110,Ensembl:ENSG00000188171 lincRNA,Protein coding intron,3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1484996241 Functional Loss SNV dbSNP153 33..33 33 - - - 2628 RMVar_ID_2628 Human_SNP_ID_661122840 A-to-I Human chr19 + 20793464 20793462 20793484 CCTGCCTCAGCCTCCCGAGTATGTGGGACTACAGGCACACATCACTATGCTCCGCTAATTTTTGT CCTGCCTCAGCCTCCCGAGTATGTGGGACTGCAGGCACACATCACTATGCTCGGCTAATTTTTGT ACAGGCACACATCACTATGCTCC GCAGGCACACATCACTATGCTCG ZNF66 Ensembl:ENSG00000160229 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs386807692 Functional Loss MNV dbSNP153 31..53 33 - - - RMVar_hsa_circ_193708,RMVar_hsa_circ_299026 2629 RMVar_ID_2629 Human_SNP_ID_661191325 A-to-I Human chr19 + 21021343 21021343 21021343 CAGCATAGTGAAACCCCGTCTTTACTAAAAATACAAAAATTTGCCGGGCATGGTGGTACACGCCT CAGCATAGTGAAACCCCGTCTTTACTAAAAATGCAAAAATTTGCCGGGCATGGTGGTACACGCCT A G ZNF430 Ensembl:ENSG00000118620 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1384623184 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121761,RMVar_hsa_circ_193711 2630 RMVar_ID_2630 Human_SNP_ID_661191479 A-to-I Human chr19 + 21021898 21021898 21021898 CGCTCTTGTCGCCCAGGCTGGAGTGCAGTGGCACAATCTCGGCTCACTACAACTTCTGCCGCTGC CGCTCTTGTCGCCCAGGCTGGAGTGCAGTGGCGCAATCTCGGCTCACTACAACTTCTGCCGCTGC A G ZNF430 Ensembl:ENSG00000118620 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1209369022 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121761,RMVar_hsa_circ_193711 2631 RMVar_ID_2631 Human_SNP_ID_661191486 A-to-I Human chr19 + 21021914 21021914 21021914 GCTGGAGTGCAGTGGCACAATCTCGGCTCACTACAACTTCTGCCGCTGCCTGTGTTCAAGCTTCT GCTGGAGTGCAGTGGCACAATCTCGGCTCACTGCAACTTCTGCCGCTGCCTGTGTTCAAGCTTCT A G ZNF430 Ensembl:ENSG00000118620 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1033563303 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121761,RMVar_hsa_circ_193711 2632 RMVar_ID_2632 Human_SNP_ID_661191517 A-to-I Human chr19 + 21022038 21022038 21022038 TTTTGTACTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCTGGCTGGCCTCGAACTCTTGACCT TTTTGTACTTTTAGTAGAGACGGGGTTTCACCGTGTTGGCCTGGCTGGCCTCGAACTCTTGACCT A G ZNF430 Ensembl:ENSG00000118620 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1004868712 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121761,RMVar_hsa_circ_193711 2633 RMVar_ID_2633 Human_SNP_ID_661194383 A-to-I Human chr19 + 21034083 21034083 21034083 ATGAGAAAGATTCATGTTATTTATTTTCAATAAAGCAGGTATTGCTGTTTCTAAGCCAGACCTGA ATGAGAAAGATTCATGTTATTTATTTTCAATACAGCAGGTATTGCTGTTTCTAAGCCAGACCTGA A C ZNF430 Ensembl:ENSG00000118620 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs768186636 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121761,RMVar_hsa_circ_193711,RMVar_hsa_circ_124203,RMVar_hsa_circ_193713,RMVar_hsa_circ_299822,RMVar_hsa_circ_193715 2634 RMVar_ID_2634 Human_SNP_ID_661210976 A-to-I Human chr19 + 21100336 21100336 21100336 CCTCAGGTCAGGAGTTCGAGATCAGCCTGACCAACATGGAGAAACCCCGTCTCTACTAAAAATAC CCTCAGGTCAGGAGTTCGAGATCAGCCTGACCGACATGGAGAAACCCCGTCTCTACTAAAAATAC A G ZNF714 Ensembl:ENSG00000160352 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1396636640 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_324022,RMVar_hsa_circ_304124 2635 RMVar_ID_2635 Human_SNP_ID_661212066 A-to-I Human chr19 + 21104742 21104742 21104742 TCCAACAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGAGATTACAGGTACCTGCCATCATGCCTG TCCAACAATTCTCCTGCCTCAGCCTCCCGAGTGGCTGAGATTACAGGTACCTGCCATCATGCCTG A G ZNF714 Ensembl:ENSG00000160352 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs966775329 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_324022,RMVar_hsa_circ_304124 2636 RMVar_ID_2636 Human_SNP_ID_661212092 A-to-I Human chr19 + 21104843 21104843 21104843 CACCATGTTGGCCAGGCTGGTCTTGAACTCCTAACTTCAGGTGATCCTACCTGACTCGGCCTCCC CACCATGTTGGCCAGGCTGGTCTTGAACTCCTGACTTCAGGTGATCCTACCTGACTCGGCCTCCC A G ZNF714 Ensembl:ENSG00000160352 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs536981387 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_324022,RMVar_hsa_circ_304124 2637 RMVar_ID_2637 Human_SNP_ID_661212295 A-to-I Human chr19 + 21105740 21105740 21105740 ACTTTGGGAGATGGAGGCGGGTGAATCACTTGAGGTCAGGAGTTGGAGACCAGCCTGGCCAACAT ACTTTGGGAGATGGAGGCGGGTGAATCACTTGTGGTCAGGAGTTGGAGACCAGCCTGGCCAACAT A T ZNF714 Ensembl:ENSG00000160352 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1428091768 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_324022,RMVar_hsa_circ_304124 2638 RMVar_ID_2638 Human_SNP_ID_661212324 A-to-I Human chr19 + 21105844 21105844 21105844 GGGCGTGCTAGTGCATGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGTTTGAA GGGCGTGCTAGTGCATGCCTGTAGTCCCAGCTGCTCGGGAGGCTGAGGCAGGAGAATTGTTTGAA A G ZNF714 Ensembl:ENSG00000160352 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs950672635 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_324022,RMVar_hsa_circ_304124 2639 RMVar_ID_2639 Human_SNP_ID_661212418 A-to-I Human chr19 + 21106170 21106170 21106170 CCACCTACTTGGGAACCTGAGGCAGGAGAATCACTTGAATCTGGGAGGCAGAGATTTCAGTGAGC CCACCTACTTGGGAACCTGAGGCAGGAGAATCGCTTGAATCTGGGAGGCAGAGATTTCAGTGAGC A G ZNF714 Ensembl:ENSG00000160352 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1209352416 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_324022,RMVar_hsa_circ_304124 2640 RMVar_ID_2640 Human_SNP_ID_661212967 A-to-I Human chr19 + 21108041 21108041 21108041 AGCCTCCTTGACTCAAGCGATCTTTCCACCTCAGCCTCCTATGTAGCTGAGACTACAGACATGCA AGCCTCCTTGACTCAAGCGATCTTTCCACCTCTGCCTCCTATGTAGCTGAGACTACAGACATGCA A T ZNF714 Ensembl:ENSG00000160352 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1219675257 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_324022,RMVar_hsa_circ_304124 2641 RMVar_ID_2641 Human_SNP_ID_661212973 A-to-I Human chr19 + 21108063 21108063 21108063 TTTCCACCTCAGCCTCCTATGTAGCTGAGACTACAGACATGCACTACCATGCCTCGCTAATTTTT TTTCCACCTCAGCCTCCTATGTAGCTGAGACTGCAGACATGCACTACCATGCCTCGCTAATTTTT A G ZNF714 Ensembl:ENSG00000160352 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1439999337 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_324022,RMVar_hsa_circ_304124 2642 RMVar_ID_2642 Human_SNP_ID_661214437 A-to-I Human chr19 + 21114273 21114273 21114273 ATCCTAGCTAACACAGTGAAACCTCGTCTACTAAAAATACAAAAAATTAGCCAGGTGTGGTGGCG ATCCTAGCTAACACAGTGAAACCTCGTCTACTGAAAATACAAAAAATTAGCCAGGTGTGGTGGCG A G ZNF714 Ensembl:ENSG00000160352 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041344577 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2585394 RMVar_hsa_circ_324022,RMVar_hsa_circ_304124 2643 RMVar_ID_2643 Human_SNP_ID_661215680 A-to-I Human chr19 + 21118250 21118250 21118250 ACTAGGTGAGCAGATCGCGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGGTAAAACCCCAT ACTAGGTGAGCAGATCGCGAGGTCAGGAGTTCCAGACCAGCCTGGCCAACATGGTAAAACCCCAT A C ZNF714 Ensembl:ENSG00000160352 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs534328825 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_324022,RMVar_hsa_circ_304124,RMVar_hsa_circ_328507 2644 RMVar_ID_2644 Human_SNP_ID_661215681 A-to-I Human chr19 + 21118250 21118250 21118250 ACTAGGTGAGCAGATCGCGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGGTAAAACCCCAT ACTAGGTGAGCAGATCGCGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTAAAACCCCAT A G ZNF714 Ensembl:ENSG00000160352 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs534328825 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_324022,RMVar_hsa_circ_304124,RMVar_hsa_circ_328507 2645 RMVar_ID_2645 Human_SNP_ID_661215691 A-to-I Human chr19 + 21118273 21118273 21118273 CAGGAGTTCAAGACCAGCCTGGCCAACATGGTAAAACCCCATCTCTACTAAAAATACAAAAATTT CAGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTT A G ZNF714 Ensembl:ENSG00000160352 Protein coding intron GSE56152 embryonic stem cells,wild type - 25708366 RNA-Seq:(High) rs757211062 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_138321 RMVar_hsa_circ_324022,RMVar_hsa_circ_304124,RMVar_hsa_circ_328507 2646 RMVar_ID_2646 Human_SNP_ID_661215696 A-to-I Human chr19 + 21118290 21118289 21118290 CCTGGCCAACATGGTAAAACCCCATCTCTACTAAAAATACAAAAATTTGCTGGGTGTGGTGGCAG CCTGGCCAACATGGTAAAACCCCATCTCTACT_AAAATACAAAAATTTGCTGGGTGTGGTGGCAG TA T ZNF714 Ensembl:ENSG00000160352 Protein coding intron GSE56152 embryonic stem cells,wild type - 25708366 RNA-Seq:(High) rs1208129611 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_324022,RMVar_hsa_circ_304124,RMVar_hsa_circ_328507 2647 RMVar_ID_2647 Human_SNP_ID_661215698 A-to-I Human chr19 + 21118290 21118290 21118290 CCTGGCCAACATGGTAAAACCCCATCTCTACTAAAAATACAAAAATTTGCTGGGTGTGGTGGCAG CCTGGCCAACATGGTAAAACCCCATCTCTACTGAAAATACAAAAATTTGCTGGGTGTGGTGGCAG A G ZNF714 Ensembl:ENSG00000160352 Protein coding intron GSE56152 embryonic stem cells,wild type - 25708366 RNA-Seq:(High) rs1320492359 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_324022,RMVar_hsa_circ_304124,RMVar_hsa_circ_328507 2648 RMVar_ID_2648 Human_SNP_ID_661215913 A-to-I Human chr19 + 21119147 21119147 21119147 AAGCTTTTGACCAGGCGTGGTGGCTCAGGCCTATAATCCCAGCACTTTGGTAGGCCAAGGCAGGT AAGCTTTTGACCAGGCGTGGTGGCTCAGGCCTGTAATCCCAGCACTTTGGTAGGCCAAGGCAGGT A G ZNF714 Ensembl:ENSG00000160352 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1158296799 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2326426,Human_miRNA_ID_2520802,Human_miRNA_ID_2775793 2649 RMVar_ID_2649 Human_SNP_ID_661215956 A-to-I Human chr19 + 21119241 21119241 21119241 CCTATCCAAGATGGTGAAACCCCATCTCTACTAAAAATACAACAATTAGCCGGTTGCGGTGGTGG CCTATCCAAGATGGTGAAACCCCATCTCTACTGAAAATACAACAATTAGCCGGTTGCGGTGGTGG A G ZNF714 Ensembl:ENSG00000160352 Protein coding intron GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs1345667925 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13408618,Human_RBP_ID_25442824 2650 RMVar_ID_2650 Human_SNP_ID_661215970 A-to-I Human chr19 + 21119295 21119294 21119296 TGCGGTGGTGGTGCCTGTAATCCCAGCTACTCAAGAGGCTGAGGCAGGAGAATCACTTGAACTTG TGCGGTGGTGGTGCCTGTAATCCCAGCTACTC__GAGGCTGAGGCAGGAGAATCACTTGAACTTG CAA C ZNF714 Ensembl:ENSG00000160352 Protein coding intron GSE47997;GSE99789;GSE99789 K562 cells&HepG2 cells;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109 - 23474544,29796672,29796672 RNA-Seq:(High) rs1252503314 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_4513387 2651 RMVar_ID_2651 Human_SNP_ID_661216124 A-to-I Human chr19 + 21120061 21120061 21120061 AGATTCTTTCTTTGTTTTGTTCTGTTTTTTTGAGATGGAGTTTTGCTCTTTCGTCCAGGCTGGAG AGATTCTTTCTTTGTTTTGTTCTGTTTTTTTGGGATGGAGTTTTGCTCTTTCGTCCAGGCTGGAG A G ZNF714 Ensembl:ENSG00000160352 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1400096484 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2560573,Human_RBP_ID_3565354,Human_RBP_ID_6729932,Human_RBP_ID_13408655,Human_RBP_ID_23309427 Human_miRNA_ID_265524,Human_miRNA_ID_1101282,Human_miRNA_ID_1528783,Human_miRNA_ID_1989128,Human_miRNA_ID_2033195,Human_miRNA_ID_2888136 2652 RMVar_ID_2652 Human_SNP_ID_661216147 A-to-I Human chr19 + 21120171 21120171 21120171 TCAAGCGATTCTCCTCCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCGCATATCACCACGCCCA TCAAGCGATTCTCCTCCCTCAGCCTCCTGAGTGGCTGGGATTACAGGCGCATATCACCACGCCCA A G ZNF714 Ensembl:ENSG00000160352 Protein coding intron GSE47997;GSE38233;GSE99789;GSE123020:GSM3490829,GSM3490830,GSM3490831 K562 cells&HepG2 cells;cultured B-cells;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109 cell line - 23474544,24183664,29796672,32596459 RNA-Seq:(High) rs1444837742 Functional Loss SNV dbSNP153 33..33 33 - - - 2653 RMVar_ID_2653 Human_SNP_ID_661216157 A-to-I Human chr19 + 21120214 21120214 21120214 CAGGCGCATATCACCACGCCCAGCTAATTTTTATGTTTCTAGTACAGACAGGATTTCATCATGTT CAGGCGCATATCACCACGCCCAGCTAATTTTTGTGTTTCTAGTACAGACAGGATTTCATCATGTT A G ZNF714 Ensembl:ENSG00000160352 Protein coding intron GSE100210;GSE99789;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;esophageal squamous carcinoma cells,EC109;ASD brains,temporal_cortex;Bronchiolar epithelium,BEP2D cell line - 29129909,29796672,30559470,31158229 RNA-Seq:(High) rs924986597 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8480936,Human_RBP_ID_17917945 2654 RMVar_ID_2654 Human_SNP_ID_661216369 A-to-I Human chr19 + 21121165 21121165 21121165 GCCATTTTCCTGCCTCAGCCTCCCAAGCAGCTAGGACTACAGGCGCCCACCACCATGCCCGGCTA GCCATTTTCCTGCCTCAGCCTCCCAAGCAGCTGGGACTACAGGCGCCCACCACCATGCCCGGCTA A G ZNF714 Ensembl:ENSG00000160352 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1443180076 Functional Loss SNV dbSNP153 33..33 33 - - - 2655 RMVar_ID_2655 Human_SNP_ID_661216393 A-to-I Human chr19 + 21121294 21121267 21121294 ACCTCGTGATCTGGTCTCGATCTCCTGACCTCATGATCTGCCTGCCTTGACCTCCCAAAGTGCTG ACCTCG___________________________TGATCTGCCTGCCTTGACCTCCCAAAGTGCTG GTGATCTGGTCTCGATCTCCTGACCTCA G ZNF714 Ensembl:ENSG00000160352 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs911776582 Functional Loss DEL dbSNP153 7..33 33 - - - Human_RBP_ID_517380,Human_RBP_ID_13408689,Human_RBP_ID_25391465,Human_RBP_ID_27465972 2656 RMVar_ID_2656 Human_SNP_ID_661216405 A-to-I Human chr19 + 21121294 21121294 21121294 ACCTCGTGATCTGGTCTCGATCTCCTGACCTCATGATCTGCCTGCCTTGACCTCCCAAAGTGCTG ACCTCGTGATCTGGTCTCGATCTCCTGACCTCGTGATCTGCCTGCCTTGACCTCCCAAAGTGCTG A G ZNF714 Ensembl:ENSG00000160352 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1001889893 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_517380,Human_RBP_ID_13408689,Human_RBP_ID_25391465,Human_RBP_ID_27465972 2657 RMVar_ID_2657 Human_SNP_ID_661216408 A-to-I Human chr19 + 21121318 21121298 21121318 CTGACCTCATGATCTGCCTGCCTTGACCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGTG CTGACCTCATGAT____________________AAGTGCTGGGATTACAGGCATGAGCCACCGTG TCTGCCTGCCTTGACCTCCCA T ZNF714 Ensembl:ENSG00000160352 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1405736148 Functional Loss DEL dbSNP153 14..33 33 - - - Human_RBP_ID_517380,Human_RBP_ID_27465974 2658 RMVar_ID_2658 Human_SNP_ID_661216643 A-to-I Human chr19 + 21122456 21122456 21122456 CTGGTGAAACCCGGTCTCTACTAATAAACTACAAAAATTAGCTGATTGTGGTGGCATCCACCTGT CTGGTGAAACCCGGTCTCTACTAATAAACTACTAAAATTAGCTGATTGTGGTGGCATCCACCTGT A T ZNF714 Ensembl:ENSG00000160352 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs780413570 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17917962,Human_RBP_ID_27465976 2659 RMVar_ID_2659 Human_SNP_ID_661216655 A-to-I Human chr19 + 21122502 21122502 21122502 TGTGGTGGCATCCACCTGTAGCCCAGCTACTCAGGAGGCTGAGGCAGAAGAATTGCTTGAACCCA TGTGGTGGCATCCACCTGTAGCCCAGCTACTCGGGAGGCTGAGGCAGAAGAATTGCTTGAACCCA A G ZNF714 Ensembl:ENSG00000160352 Protein coding intron GSE47997;GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line - 23474544,24183664,29129909,29796672,31158229 RNA-Seq:(High) rs909519087 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_517393,Human_RBP_ID_2560600,Human_RBP_ID_8480946,Human_RBP_ID_13408744 2660 RMVar_ID_2660 Human_SNP_ID_661216922 A-to-I Human chr19 + 21123403 21123403 21123403 TAGAGACAGAGTCTTGCTCTGTCTCCCAGGCTAGAGTACAGTGGTGTGATCTTGGCTCACTGCAA TAGAGACAGAGTCTTGCTCTGTCTCCCAGGCTGGAGTACAGTGGTGTGATCTTGGCTCACTGCAA A G ZNF714 Ensembl:ENSG00000160352 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs1433157409 Functional Loss SNV dbSNP153 33..33 33 - - - 2661 RMVar_ID_2661 Human_SNP_ID_661216976 A-to-I Human chr19 + 21123531 21123531 21123531 CGCCCGCTACCGCACCCGTCTAATTTTTTTGTATTTTTAGTAGAGACGGGATTTCACCATGTTAG CGCCCGCTACCGCACCCGTCTAATTTTTTTGTGTTTTTAGTAGAGACGGGATTTCACCATGTTAG A G ZNF714 Ensembl:ENSG00000160352 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs990733007 Functional Loss SNV dbSNP153 33..33 33 - - - 2662 RMVar_ID_2662 Human_SNP_ID_661216977 A-to-I Human chr19 + 21123537 21123537 21123537 CTACCGCACCCGTCTAATTTTTTTGTATTTTTAGTAGAGACGGGATTTCACCATGTTAGCCAGGA CTACCGCACCCGTCTAATTTTTTTGTATTTTTGGTAGAGACGGGATTTCACCATGTTAGCCAGGA A G ZNF714 Ensembl:ENSG00000160352 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs1469944469 Functional Loss SNV dbSNP153 33..33 33 - - - 2663 RMVar_ID_2663 Human_SNP_ID_661216983 A-to-I Human chr19 + 21123562 21123562 21123562 TATTTTTAGTAGAGACGGGATTTCACCATGTTAGCCAGGATGGTCTCAATCTCCTGACCTCGTGA TATTTTTAGTAGAGACGGGATTTCACCATGTTGGCCAGGATGGTCTCAATCTCCTGACCTCGTGA A G ZNF714 Ensembl:ENSG00000160352 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1462872051 Functional Loss SNV dbSNP153 33..33 33 - - - 2664 RMVar_ID_2664 Human_SNP_ID_661216987 A-to-I Human chr19 + 21123577 21123577 21123577 CGGGATTTCACCATGTTAGCCAGGATGGTCTCAATCTCCTGACCTCGTGATCCGCCCGCCTCGAC CGGGATTTCACCATGTTAGCCAGGATGGTCTCCATCTCCTGACCTCGTGATCCGCCCGCCTCGAC A C ZNF714 Ensembl:ENSG00000160352 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs533260671 Functional Loss SNV dbSNP153 33..33 33 - - - 2665 RMVar_ID_2665 Human_SNP_ID_661222668 A-to-I Human chr19 + 21147237 21147237 21147237 TGCTGGGCACAGTGGCTCCTGCCTGTAATCTCAGCCCTTTGGGAGGCCAAGGCAGGTGGATTATC TGCTGGGCACAGTGGCTCCTGCCTGTAATCTCGGCCCTTTGGGAGGCCAAGGCAGGTGGATTATC A G ZNF431 Ensembl:ENSG00000196705 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1221160091 Functional Loss SNV dbSNP153 33..33 33 - - - 2666 RMVar_ID_2666 Human_SNP_ID_661229008 A-to-I Human chr19 + 21172273 21172273 21172273 CAATATGGTGAAACCCTGTCTCTACTAAAAATACAAAATTAGCCAGACATGGTGGTGTATGTGTG CAATATGGTGAAACCCTGTCTCTACTAAAAATGCAAAATTAGCCAGACATGGTGGTGTATGTGTG A G ZNF431 Ensembl:ENSG00000196705 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1160003278 Functional Loss SNV dbSNP153 33..33 33 - - - 2667 RMVar_ID_2667 Human_SNP_ID_661229652 A-to-I Human chr19 + 21174890 21174890 21174890 CACCTCCTAGATTCAAGCGATATTCCTTCCTCAGCCTCCCAAGTAGCTGGGAGTACAGGTGTAGT CACCTCCTAGATTCAAGCGATATTCCTTCCTCGGCCTCCCAAGTAGCTGGGAGTACAGGTGTAGT A G ZNF431 Ensembl:ENSG00000196705 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs920940425 Functional Loss SNV dbSNP153 33..33 33 - - - 2668 RMVar_ID_2668 Human_SNP_ID_661229722 A-to-I Human chr19 + 21175077 21175077 21175077 CTGCACCTGGCCAATGTATTTATTTTTGAGATAAAGTCTCACTCTGTCATCCAGGCTGGTTTGCA CTGCACCTGGCCAATGTATTTATTTTTGAGATGAAGTCTCACTCTGTCATCCAGGCTGGTTTGCA A G ZNF431 Ensembl:ENSG00000196705 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1001670874 Functional Loss SNV dbSNP153 33..33 33 - - - 2669 RMVar_ID_2669 Human_SNP_ID_661230082 A-to-I Human chr19 + 21176380 21176380 21176380 CTTCTGCCTCAGCCTCCTGAGTAGCTGGCATTACAGGCATGTGCCACCATGCCTGGCTAATTTTT CTTCTGCCTCAGCCTCCTGAGTAGCTGGCATTCCAGGCATGTGCCACCATGCCTGGCTAATTTTT A C ZNF431 Ensembl:ENSG00000196705 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1475691577 Functional Loss SNV dbSNP153 33..33 33 - - - 2670 RMVar_ID_2670 Human_SNP_ID_661230109 A-to-I Human chr19 + 21176504 21176504 21176504 GTCTCAGGTGATCCTCCCACCTCGGCCTCCCAAAGTGCTGGGATTATAGCCGTGAGCCACTGTGC GTCTCAGGTGATCCTCCCACCTCGGCCTCCCAGAGTGCTGGGATTATAGCCGTGAGCCACTGTGC A G ZNF431 Ensembl:ENSG00000196705 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs549182641 Functional Loss SNV dbSNP153 33..33 33 - - - 2671 RMVar_ID_2671 Human_SNP_ID_661232174 A-to-I Human chr19 + 21184284 21184283 21184284 AGGCAGGATAATCACTTGAACCTGGGAGGTGGAAGTTGCAGTGAGCCAAGATTGTACCACTGCAC AGGCAGGATAATCACTTGAACCTGGGAGGTGG_AGTTGCAGTGAGCCAAGATTGTACCACTGCAC GA G ZNF431 Ensembl:ENSG00000196705 Protein coding intron GSE47997;GSE38233;GSE123020:GSM3490829,GSM3490830,GSM3490831 K562 cells&HepG2 cells;cultured B-cells;esophageal squamous carcinoma cells,EC109 cell line - 23474544,24183664,32596459 RNA-Seq:(High) rs541552375 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_8480995 RMVar_hsa_circ_8672 2672 RMVar_ID_2672 Human_SNP_ID_661232491 A-to-I Human chr19 + 21185522 21185522 21185522 TCACTCTTTCGCCCAGGCTGGAGTGCATTGGCATGATCTCAGCTCACTACAACCTCTGCCTTCTG TCACTCTTTCGCCCAGGCTGGAGTGCATTGGCGTGATCTCAGCTCACTACAACCTCTGCCTTCTG A G ZNF431 Ensembl:ENSG00000196705 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs960404617 Functional Loss SNV dbSNP153 33..33 33 - - - 2673 RMVar_ID_2673 Human_SNP_ID_661232493 A-to-I Human chr19 + 21185538 21185538 21185538 GCTGGAGTGCATTGGCATGATCTCAGCTCACTACAACCTCTGCCTTCTGGTTTCAAGCAACTCTT GCTGGAGTGCATTGGCATGATCTCAGCTCACTGCAACCTCTGCCTTCTGGTTTCAAGCAACTCTT A G ZNF431 Ensembl:ENSG00000196705 Protein coding intron GSE38233;GSE100210;GSE99789 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 24183664,29129909,29796672 RNA-Seq:(High) rs1395026020 Functional Loss SNV dbSNP153 33..33 33 - - - 2674 RMVar_ID_2674 Human_SNP_ID_661232499 A-to-I Human chr19 + 21185590 21185590 21185590 TCAAGCAACTCTTCTGCCTCAGCATCCCAAGTAGCTGGGATAACAGGTGCCAGCCACCATGCCCA TCAAGCAACTCTTCTGCCTCAGCATCCCAAGTTGCTGGGATAACAGGTGCCAGCCACCATGCCCA A T ZNF431 Ensembl:ENSG00000196705 Protein coding intron GSE38233;GSE99789 cultured B-cells;esophageal squamous carcinoma cells,EC109 - 24183664,29796672 RNA-Seq:(High) rs991915898 Functional Loss SNV dbSNP153 33..33 33 - - - 2675 RMVar_ID_2675 Human_SNP_ID_661232515 A-to-I Human chr19 + 21185641 21185641 21185641 AGCCACCATGCCCAGCTAATTTGTGTATTTCTAGTAGAGATGGGGTTTCACCATATTGGCCAAGC AGCCACCATGCCCAGCTAATTTGTGTATTTCTGGTAGAGATGGGGTTTCACCATATTGGCCAAGC A G ZNF431 Ensembl:ENSG00000196705 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs532131974 Functional Loss SNV dbSNP153 33..33 33 - - - 2676 RMVar_ID_2676 Human_SNP_ID_661232523 A-to-I Human chr19 + 21185663 21185663 21185663 GTGTATTTCTAGTAGAGATGGGGTTTCACCATATTGGCCAAGCTGGTCTTGAACTCCTGACCTCA GTGTATTTCTAGTAGAGATGGGGTTTCACCATGTTGGCCAAGCTGGTCTTGAACTCCTGACCTCA A G ZNF431 Ensembl:ENSG00000196705 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1039757266 Functional Loss SNV dbSNP153 33..33 33 - - - 2677 RMVar_ID_2677 Human_SNP_ID_661233741 A-to-I Human chr19 + 21190124 21190124 21190124 CACAGATGCAGAGGTTGCAGTGAACTGAGATCATGCCACTGCACTCCATCCTGGGCAACAGAGTG CACAGATGCAGAGGTTGCAGTGAACTGAGATCGTGCCACTGCACTCCATCCTGGGCAACAGAGTG A G ZNF431 Ensembl:ENSG00000196705 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1382736723 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_517498,Human_RBP_ID_25391759 2678 RMVar_ID_2678 Human_SNP_ID_661234082 A-to-I Human chr19 + 21191330 21191330 21191330 CAAATATTAGCCGGGCGTGGTTGCACGTGTCTATAATCTCAGCTACTCAGGAGGCTGAGGCAGGG CAAATATTAGCCGGGCGTGGTTGCACGTGTCTGTAATCTCAGCTACTCAGGAGGCTGAGGCAGGG A G ZNF431 Ensembl:ENSG00000196705 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs747993606 Functional Loss SNV dbSNP153 33..33 33 - - - 2679 RMVar_ID_2679 Human_SNP_ID_661234083 A-to-I Human chr19 + 21191332 21191332 21191332 AATATTAGCCGGGCGTGGTTGCACGTGTCTATAATCTCAGCTACTCAGGAGGCTGAGGCAGGGGA AATATTAGCCGGGCGTGGTTGCACGTGTCTATGATCTCAGCTACTCAGGAGGCTGAGGCAGGGGA A G ZNF431 Ensembl:ENSG00000196705 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1384386720 Functional Loss SNV dbSNP153 33..33 33 - - - 2680 RMVar_ID_2680 Human_SNP_ID_661234279 A-to-I Human chr19 + 21192174 21192166 21192174 TATTTTGAAAGTTTAATAAATTTTGTTTATTTATTTATTTATTTTGAGATGGAGTCTCGGTCTGT TATTTTGAAAGTTTAATAAATTTTG________TTTATTTATTTTGAGATGGAGTCTCGGTCTGT GTTTATTTA G ZNF431 Ensembl:ENSG00000196705 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749176908 Functional Loss DEL dbSNP153 26..33 33 - - - Human_RBP_ID_6730476,Human_RBP_ID_26651588 2681 RMVar_ID_2681 Human_SNP_ID_661234280 A-to-I Human chr19 + 21192174 21192166 21192174 TATTTTGAAAGTTTAATAAATTTTGTTTATTTATTTATTTATTTTGAGATGGAGTCTCGGTCTGT TATTTTGAAAGTTTAATAAATTTTGTTTA____TTTATTTATTTTGAGATGGAGTCTCGGTCTGT GTTTATTTA GTTTA ZNF431 Ensembl:ENSG00000196705 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749176908 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_6730476,Human_RBP_ID_26651588 2682 RMVar_ID_2682 Human_SNP_ID_661234282 A-to-I Human chr19 + 21192174 21192174 21192174 TATTTTGAAAGTTTAATAAATTTTGTTTATTTATTTATTTATTTTGAGATGGAGTCTCGGTCTGT TATTTTGAAAGTTTAATAAATTTTGTTTATTTTTTTATTTATTTTGAGATGGAGTCTCGGTCTGT A T ZNF431 Ensembl:ENSG00000196705 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041678387 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6730476,Human_RBP_ID_26651588 2683 RMVar_ID_2683 Human_SNP_ID_661258307 A-to-I Human chr19 - 21290112 21290112 21290112 CGCCACCACACCCAGCTAATTTTTGTATTTTTAGTAGAGACCAGGGTTTCCCCATATTGGGCAGG CGCCACCACACCCAGCTAATTTTTGTATTTTTGGTAGAGACCAGGGTTTCCCCATATTGGGCAGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1465973889 Functional Loss SNV dbSNP153 33..33 33 - - - 2684 RMVar_ID_2684 Human_SNP_ID_661258726 A-to-I Human chr19 - 21291813 21291813 21291813 TCGTCCAGGCTGGAGTGCAGTGGCACAATCTCAGCTCGCTGCAACCTCTGCCTCCTGGGTTCAAG TCGTCCAGGCTGGAGTGCAGTGGCACAATCTCGGCTCGCTGCAACCTCTGCCTCCTGGGTTCAAG T C ZNF708 Ensembl:ENSG00000182141 Protein coding 3'UTR GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs535666875 Functional Loss SNV dbSNP153 33..33 33 - - - 2685 RMVar_ID_2685 Human_SNP_ID_661258828 A-to-I Human chr19 - 21292205 21292205 21292205 CAACATGGTAAAACCCTGTCTCTACTAAAAATACAAAAATTAGCTGGGCGTGGCGGCACGTGCCT CAACATGGTAAAACCCTGTCTCTACTAAAAATCCAAAAATTAGCTGGGCGTGGCGGCACGTGCCT T G ZNF708 Ensembl:ENSG00000182141 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1224778962 Functional Loss SNV dbSNP153 33..33 33 - - - 2686 RMVar_ID_2686 Human_SNP_ID_661258836 A-to-I Human chr19 - 21292228 21292228 21292228 CAACAGATTGAGACCATCCTGGTCAACATGGTAAAACCCTGTCTCTACTAAAAATACAAAAATTA CAACAGATTGAGACCATCCTGGTCAACATGGTGAAACCCTGTCTCTACTAAAAATACAAAAATTA T C ZNF708 Ensembl:ENSG00000182141 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs878915331 Functional Loss SNV dbSNP153 33..33 33 - - - 2687 RMVar_ID_2687 Human_SNP_ID_661261547 A-to-I Human chr19 - 21301294 21301294 21301294 TTGTATTTTTTTAGTAGAGATCGGGATTCACTATGTTGGCCAGGCTGGTCTTGAACTCATGACCT TTGTATTTTTTTAGTAGAGATCGGGATTCACTGTGTTGGCCAGGCTGGTCTTGAACTCATGACCT T C ZNF708 Ensembl:ENSG00000182141 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984753167 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13410283 2688 RMVar_ID_2688 Human_SNP_ID_661280824 A-to-I Human chr19 + 21376657 21376657 21376657 TCATCGTAACCTCTGCCTCCAGCGATTCTCCTATGTCAGCCTCCCGAGTAGCTGAGACTACAGGC TCATCGTAACCTCTGCCTCCAGCGATTCTCCTGTGTCAGCCTCCCGAGTAGCTGAGACTACAGGC A G ZNF738 Ensembl:ENSG00000172687 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,cerebellum - 29129909,30559470 RNA-Seq:(High) rs905241631 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2560889,Human_RBP_ID_6730848 RMVar_hsa_circ_89991,RMVar_hsa_circ_193723 2689 RMVar_ID_2689 Human_SNP_ID_661280829 A-to-I Human chr19 + 21376674 21376674 21376674 TCCAGCGATTCTCCTATGTCAGCCTCCCGAGTAGCTGAGACTACAGGCATGCACCACCATGAGAG TCCAGCGATTCTCCTATGTCAGCCTCCCGAGTGGCTGAGACTACAGGCATGCACCACCATGAGAG A G ZNF738 Ensembl:ENSG00000172687 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,cerebellum - 29129909,30559470 RNA-Seq:(High) rs1300025418 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89991,RMVar_hsa_circ_193723 2690 RMVar_ID_2690 Human_SNP_ID_661281424 A-to-I Human chr19 + 21378875 21378875 21378875 CCCACCTCAGCTTCCCAAAGTGCCGGGATTACAAGCTTGAGCTACCGCGCCCAGCCAACACATCA CCCACCTCAGCTTCCCAAAGTGCCGGGATTACTAGCTTGAGCTACCGCGCCCAGCCAACACATCA A T ZNF738 Ensembl:ENSG00000172687 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs927545933 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_517572,Human_RBP_ID_3565562,Human_RBP_ID_13410807 RMVar_hsa_circ_89991,RMVar_hsa_circ_193723 2691 RMVar_ID_2691 Human_SNP_ID_661281642 A-to-I Human chr19 + 21379969 21379969 21379969 TATGTGTCATCTCATAGAATACTTAATATGTCAAACCCAGGAAAATCAGTAACTAAGTAACAAAA TATGTGTCATCTCATAGAATACTTAATATGTCTAACCCAGGAAAATCAGTAACTAAGTAACAAAA A T - - Other Unknown GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs189816252 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89991,RMVar_hsa_circ_193723 2692 RMVar_ID_2692 Human_SNP_ID_661288355 A-to-I Human chr19 + 21406034 21406034 21406034 CCTGAGCTCAGGAGTTCGAGACCAGACTGGCCAACATGGTGTAAACTCTGTCTCTACTAAAAATA CCTGAGCTCAGGAGTTCGAGACCAGACTGGCCGACATGGTGTAAACTCTGTCTCTACTAAAAATA A G AC010615.4,ZNF493 Ensembl:ENSG00000269237,Ensembl:ENSG00000196268 Protein coding,Protein coding intron,intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs530720776 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96953,RMVar_hsa_circ_193725 2693 RMVar_ID_2693 Human_SNP_ID_661288720 A-to-I Human chr19 + 21407428 21407428 21407428 CACCTGCATTAGCCTCCCGAGTAGCTGGGACTACAGGCACCTGCCACCATGCCTGGCTAATTTTT CACCTGCATTAGCCTCCCGAGTAGCTGGGACTGCAGGCACCTGCCACCATGCCTGGCTAATTTTT A G AC010615.4,ZNF493 Ensembl:ENSG00000269237,Ensembl:ENSG00000196268 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1467475255 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96953,RMVar_hsa_circ_193725 2694 RMVar_ID_2694 Human_SNP_ID_661289915 A-to-I Human chr19 + 21411458 21411458 21411458 AAATGTTAAGCAGGTTGGGTGCGCTGTCTCACACCTGTAATCCCAACAGTTTGGGAGGCTGAGGC AAATGTTAAGCAGGTTGGGTGCGCTGTCTCACGCCTGTAATCCCAACAGTTTGGGAGGCTGAGGC A G AC010615.4,ZNF493 Ensembl:ENSG00000269237,Ensembl:ENSG00000196268 Protein coding,Protein coding intron,intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs752850748 Functional Loss SNV dbSNP153 33..33 33 - - - 2695 RMVar_ID_2695 Human_SNP_ID_661294042 A-to-I Human chr19 - 21424324 21424324 21424324 ATTCTCTTATGTGTAGTAAGGTGTGAGGACCGATTAAAAGCTTTGCCACATTCTTCACATTTGTA ATTCTCTTATGTGTAGTAAGGTGTGAGGACCGCTTAAAAGCTTTGCCACATTCTTCACATTTGTA T G lnc-ZNF708-1 RNACentral:URS00008BE838 lincRNA intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1214962670 Functional Loss SNV dbSNP153 33..33 33 - - - 2696 RMVar_ID_2696 Human_SNP_ID_661294043 A-to-I Human chr19 - 21424324 21424324 21424324 ATTCTCTTATGTGTAGTAAGGTGTGAGGACCGATTAAAAGCTTTGCCACATTCTTCACATTTGTA ATTCTCTTATGTGTAGTAAGGTGTGAGGACCGTTTAAAAGCTTTGCCACATTCTTCACATTTGTA T A lnc-ZNF708-1 RNACentral:URS00008BE838 lincRNA intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) - Functional Loss SNV HGVD 33..33 33 - - - 2697 RMVar_ID_2697 Human_SNP_ID_661385100 A-to-I Human chr19 - 21736126 21736126 21736126 CCAAGATCGCGCCATTGCACTCTAGCATGGGCAACAGAGTGAGATTCCATCTCAAAAAAATAAAT CCAAGATCGCGCCATTGCACTCTAGCATGGGCGACAGAGTGAGATTCCATCTCAAAAAAATAAAT T C ZNF100 Ensembl:ENSG00000197020 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10405142 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269355 2698 RMVar_ID_2698 Human_SNP_ID_661386622 A-to-I Human chr19 - 21742210 21742210 21742210 TCACTGCAACCCCCACCTCCTGGGTTCAAGCAATTCTCCTGCCTCAGCGTCCCGAGTAGCTGGGA TCACTGCAACCCCCACCTCCTGGGTTCAAGCAGTTCTCCTGCCTCAGCGTCCCGAGTAGCTGGGA T C ZNF100 Ensembl:ENSG00000197020 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs542117576 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269355 2699 RMVar_ID_2699 Human_SNP_ID_661386623 A-to-I Human chr19 - 21742211 21742211 21742211 CTCACTGCAACCCCCACCTCCTGGGTTCAAGCAATTCTCCTGCCTCAGCGTCCCGAGTAGCTGGG CTCACTGCAACCCCCACCTCCTGGGTTCAAGCGATTCTCCTGCCTCAGCGTCCCGAGTAGCTGGG T C ZNF100 Ensembl:ENSG00000197020 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1485550608 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269355 2700 RMVar_ID_2700 Human_SNP_ID_661402383 A-to-I Human chr19 - 21806237 21806237 21806237 GGAAAGTGGAGGTCTCAGTGAGCCGAAATCATACCATTGCACTCCAACCTGGGCAACAAAAGTCA GGAAAGTGGAGGTCTCAGTGAGCCGAAATCATTCCATTGCACTCCAACCTGGGCAACAAAAGTCA T A ZNF43 Ensembl:ENSG00000198521 Protein coding 3'UTR GSE107867 ASD brains,frontal_cortex;ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1266566678 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17918236 2701 RMVar_ID_2701 Human_SNP_ID_661402425 A-to-I Human chr19 - 21806438 21806438 21806438 AGATGCAGCCAGGCATGGTGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCTGAGGCCGGTGG AGATGCAGCCAGGCATGGTGGCTCATGCCTATGATCCCAGCACTTTGGGAGGCTGAGGCCGGTGG T C ZNF43 Ensembl:ENSG00000198521 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1027565815 Functional Loss SNV dbSNP153 33..33 33 - - - 2702 RMVar_ID_2702 Human_SNP_ID_661402426 A-to-I Human chr19 - 21806440 21806440 21806440 TAAGATGCAGCCAGGCATGGTGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCTGAGGCCGGT TAAGATGCAGCCAGGCATGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCCGGT T C ZNF43 Ensembl:ENSG00000198521 Protein coding 3'UTR GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1270865805 Functional Loss SNV dbSNP153 33..33 33 - - - 2703 RMVar_ID_2703 Human_SNP_ID_661409560 A-to-I Human chr19 - 21832699 21832699 21832699 CACCACGCCCAGCTAATTTTTGTATTTTTGGTAGAGATGGGGTTTCACCATATTGGCCCGGCTGG CACCACGCCCAGCTAATTTTTGTATTTTTGGTGGAGATGGGGTTTCACCATATTGGCCCGGCTGG T C ZNF43 Ensembl:ENSG00000198521 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1284363197 Functional Loss SNV dbSNP153 33..33 33 - - - 2704 RMVar_ID_2704 Human_SNP_ID_661409898 A-to-I Human chr19 - 21833865 21833865 21833865 GCACTACCACGCCTGGCTAATTTTGCATTTTTAGTAGAGACAGGGTTTCCCCATGTTGGTCACGC GCACTACCACGCCTGGCTAATTTTGCATTTTTGGTAGAGACAGGGTTTCCCCATGTTGGTCACGC T C ZNF43 Ensembl:ENSG00000198521 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs887340838 Functional Loss SNV dbSNP153 33..33 33 - - - 2705 RMVar_ID_2705 Human_SNP_ID_661410468 A-to-I Human chr19 - 21835558 21835558 21835558 GAGGTGAGGAGTTCGAGAGCAGCCTGGCTAATATGGTGAACCCCGTCTATACTAAAAATACAAAA GAGGTGAGGAGTTCGAGAGCAGCCTGGCTAATGTGGTGAACCCCGTCTATACTAAAAATACAAAA T C ZNF43 Ensembl:ENSG00000198521 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs892238348 Functional Loss SNV dbSNP153 33..33 33 - - - 2706 RMVar_ID_2706 Human_SNP_ID_661412192 A-to-I Human chr19 - 21841805 21841805 21841805 CTAATAGAGGAATTATGACATGTCATTTGTTTATCACCTAAGTGATGTAACTTCTACCTGAACCC CTAATAGAGGAATTATGACATGTCATTTGTTTGTCACCTAAGTGATGTAACTTCTACCTGAACCC T C ZNF43 Ensembl:ENSG00000198521 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1473848786 Functional Loss SNV dbSNP153 33..33 33 - - - 2707 RMVar_ID_2707 Human_SNP_ID_661412196 A-to-I Human chr19 - 21841823 21841823 21841823 TGGGACTCTCTTCACCTGCTAATAGAGGAATTATGACATGTCATTTGTTTATCACCTAAGTGATG TGGGACTCTCTTCACCTGCTAATAGAGGAATTGTGACATGTCATTTGTTTATCACCTAAGTGATG T C ZNF43 Ensembl:ENSG00000198521 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs372204431 Functional Loss SNV dbSNP153 33..33 33 - - - 2708 RMVar_ID_2708 Human_SNP_ID_661413750 A-to-I Human chr19 - 21847658 21847658 21847658 GAGTCTCACTCTGTTGCACAGGCTGGAGTGCAATGTTGTGATCTTGGCTTACTGCAACCTCCGCC GAGTCTCACTCTGTTGCACAGGCTGGAGTGCAGTGTTGTGATCTTGGCTTACTGCAACCTCCGCC T C ZNF43 Ensembl:ENSG00000198521 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1372680465 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13412341 2709 RMVar_ID_2709 Human_SNP_ID_661413908 A-to-I Human chr19 - 21848174 21848174 21848174 ACACCACTGCACTCCAGCCTGGGCAACAGAGCAAGACTCTGTCTCAAAAAACAACAACAACAACA ACACCACTGCACTCCAGCCTGGGCAACAGAGCGAGACTCTGTCTCAAAAAACAACAACAACAACA T C ZNF43 Ensembl:ENSG00000198521 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1486230624 Functional Loss SNV dbSNP153 33..33 33 - - - 2710 RMVar_ID_2710 Human_SNP_ID_661413909 A-to-I Human chr19 - 21848174 21848174 21848174 ACACCACTGCACTCCAGCCTGGGCAACAGAGCAAGACTCTGTCTCAAAAAACAACAACAACAACA ACACCACTGCACTCCAGCCTGGGCAACAGAGCCAGACTCTGTCTCAAAAAACAACAACAACAACA T G ZNF43 Ensembl:ENSG00000198521 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1486230624 Functional Loss SNV dbSNP153 33..33 33 - - - 2711 RMVar_ID_2711 Human_SNP_ID_661748518 A-to-I Human chr19 - 23126982 23126982 23126982 ATATACGCAAGTTTTTTCTCAAAGTTTCAGAAATGTTTGATAAAACAAGAAAAATAGAAGCATGA ATATACGCAAGTTTTTTCTCAAAGTTTCAGAACTGTTTGATAAAACAAGAAAAATAGAAGCATGA T G SNX6P1 Ensembl:ENSG00000267920 Pseudogene exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs879246618 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2561047,Human_RBP_ID_5586202 2712 RMVar_ID_2712 Human_SNP_ID_661776293 A-to-I Human chr19 - 23221677 23221675 23221677 TACTCGGTGGTTGAGACAGGAGAATCGCTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCTGAGTT TACTCGGTGGTTGAGACAGGAGAATCGCTTGA__CTGGGAGGCAGAGGTTGCAGTGAGCTGAGTT GGT G ZNF724 Ensembl:ENSG00000196081 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,31158229,31158229 RNA-Seq:(High) rs1461214305 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_6732468 2713 RMVar_ID_2713 Human_SNP_ID_661779005 A-to-I Human chr19 - 23231062 23231062 23231062 CCTGACCAACATGGAGAAACCCCGTCTTTACTAAAAATACAAAATTAGCTGGGTGTGGTGGCGCA CCTGACCAACATGGAGAAACCCCGTCTTTACTGAAAATACAAAATTAGCTGGGTGTGGTGGCGCA T C AC092329.3,ZNF724 Ensembl:ENSG00000283201,Ensembl:ENSG00000196081 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1450746058 Functional Loss SNV dbSNP153 33..33 33 - - - 2714 RMVar_ID_2714 Human_SNP_ID_661785650 A-to-I Human chr19 - 23255600 23255600 23255600 AAAATTAGCTGGGCGTGGTGGCAGGCGCCTGTAGTTCCAGCCACCCACGAGGCTGAGGCAGGAGA AAAATTAGCTGGGCGTGGTGGCAGGCGCCTGTCGTTCCAGCCACCCACGAGGCTGAGGCAGGAGA T G IPO5P1,AC092329.3 Ensembl:ENSG00000269837,Ensembl:ENSG00000283201 Pseudogene,Protein coding exon,intron GSE38233;GSE107867;GSE107867 cultured B-cells;ASD brains,cerebellum;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 24183664,30559470,30559470 RNA-Seq:(High) rs1234008544 Functional Loss SNV dbSNP153 33..33 33 - - - 2715 RMVar_ID_2715 Human_SNP_ID_661785677 A-to-I Human chr19 - 23255689 23255689 23255689 TGGGAGGCCGAGGCGAGTGGATACCTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGA TGGGAGGCCGAGGCGAGTGGATACCTGAGGTCCGGAGTTCGAGACCAGCCTGGCCAACATGGTGA T G IPO5P1,AC092329.3 Ensembl:ENSG00000269837,Ensembl:ENSG00000283201 Pseudogene,Protein coding exon,intron GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs1434243754 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17387931 2716 RMVar_ID_2716 Human_SNP_ID_661785692 A-to-I Human chr19 - 23255740 23255740 23255740 AATTGTGACCTTGGCCAGGCTCGGTGGCTCACACCTGTAATCATAGCACTTTGGGAGGCCGAGGC AATTGTGACCTTGGCCAGGCTCGGTGGCTCACCCCTGTAATCATAGCACTTTGGGAGGCCGAGGC T G IPO5P1,AC092329.3 Ensembl:ENSG00000269837,Ensembl:ENSG00000283201 Pseudogene,Protein coding exon,intron GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs927198546 Functional Loss SNV dbSNP153 33..33 33 - - - 2717 RMVar_ID_2717 Human_SNP_ID_661786217 A-to-I Human chr19 - 23257838 23257838 23257838 AAACTCTTGACCTCAGGTGATGCACCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG AAACTCTTGACCTCAGGTGATGCACCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG T C IPO5P1,AC092329.1,AC092329.3 Ensembl:ENSG00000269837,Ensembl:ENSG00000269107,Ensembl:ENSG00000283201 Pseudogene,lincRNA,Protein coding exon,intron,intron GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs1021804528 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13543202,Human_RBP_ID_17568015 2718 RMVar_ID_2718 Human_SNP_ID_661786433 A-to-I Human chr19 - 23258499 23258499 23258499 GCCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAATCGGGTGTGGTGGCGGGCAC GCCAACATGGTGAAACCCCGTCTCTACTAAAAGTACAAAAATTAATCGGGTGTGGTGGCGGGCAC T C AC092329.1,AC092329.3 Ensembl:ENSG00000269107,Ensembl:ENSG00000283201 lincRNA,Protein coding intron,intron GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs1225962355 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25392656 2719 RMVar_ID_2719 Human_SNP_ID_661787989 A-to-I Human chr19 - 23264871 23264871 23264871 TTGCACTGTCGCCTGGGCTGCAGTGCAGTGGCATGATCTTGGCTCACCACAACCTCCGCCTCCCG TTGCACTGTCGCCTGGGCTGCAGTGCAGTGGCGTGATCTTGGCTCACCACAACCTCCGCCTCCCG T C AC092329.1,AC092329.4,AC092329.3 Ensembl:ENSG00000269107,Ensembl:ENSG00000284428,Ensembl:ENSG00000283201 lincRNA,lincRNA,Protein coding intron,intron,intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1213232980 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6732607,Human_RBP_ID_13414355 2720 RMVar_ID_2720 Human_SNP_ID_661807506 A-to-I Human chr19 - 23338863 23338863 23338863 ATTTTCAGAAGAGACGGGGTTTCATCATATTCACCAGGCTGGTCTTGATCTCTTGACCTCGTGAT ATTTTCAGAAGAGACGGGGTTTCATCATATTCGCCAGGCTGGTCTTGATCTCTTGACCTCGTGAT T C ZNF91 Ensembl:ENSG00000167232 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1013270653 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2561139,Human_RBP_ID_27675805 RMVar_hsa_circ_193757,RMVar_hsa_circ_193758 2721 RMVar_ID_2721 Human_SNP_ID_661807507 A-to-I Human chr19 - 23338867 23338864 23338868 TTGTATTTTCAGAAGAGACGGGGTTTCATCATATTCACCAGGCTGGTCTTGATCTCTTGACCTCG TTGTATTTTCAGAAGAGACGGGGTTTCATCA____CACCAGGCTGGTCTTGATCTCTTGACCTCG GAATA G ZNF91 Ensembl:ENSG00000167232 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs746789426 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_2561139,Human_RBP_ID_27675805 RMVar_hsa_circ_193757,RMVar_hsa_circ_193758 2722 RMVar_ID_2722 Human_SNP_ID_661808140 A-to-I Human chr19 - 23341183 23341183 23341183 AGCCAGGCGTGGTGGCACTTGCCTGCAGCCCCAACTCCTCAGGAGGCTGACACAGAAGAATTGCT AGCCAGGCGTGGTGGCACTTGCCTGCAGCCCCGACTCCTCAGGAGGCTGACACAGAAGAATTGCT T C ZNF91 Ensembl:ENSG00000167232 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982223096 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193757,RMVar_hsa_circ_193758 2723 RMVar_ID_2723 Human_SNP_ID_661813443 A-to-I Human chr19 - 23361268 23361268 23361268 CCCTTACTACACATAAAATAATTCATGCTGGAAAGAAACTCTACAAATGTGAAGAATGTGGCAAA CCCTTACTACACATAAAATAATTCATGCTGGAGAGAAACTCTACAAATGTGAAGAATGTGGCAAA T C ZNF91 Ensembl:ENSG00000167232 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs775185517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8096199,Human_RBP_ID_9085513 Human_miRNA_ID_217178,Human_miRNA_ID_661869,Human_miRNA_ID_668061,Human_miRNA_ID_673145 RMVar_hsa_circ_193761,RMVar_hsa_circ_193757,RMVar_hsa_circ_193758,RMVar_hsa_circ_193760,RMVar_hsa_circ_193759,RMVar_hsa_circ_193763,RMVar_hsa_circ_193764,RMVar_hsa_circ_193765,RMVar_hsa_circ_193762 2724 RMVar_ID_2724 Human_SNP_ID_661815598 A-to-I Human chr19 - 23368352 23368350 23368352 TGCCGCCCCGCCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGTTTTCACCATCTTGTTCAGGC TGCCGCCCCGCCTGGCTAATTTTTGTATTTTT__TAGAGACAGGTTTTCACCATCTTGTTCAGGC ACT A ZNF91 Ensembl:ENSG00000167232 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs566684451 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_13414660 RMVar_hsa_circ_193761,RMVar_hsa_circ_193762 2725 RMVar_ID_2725 Human_SNP_ID_661816444 A-to-I Human chr19 - 23370538 23370538 23370538 ATAATGTGCCACTCTACTCAAGCTTGTGTGACAGATTGAGACCCTGTCTCAAAAAACTAAACAAA ATAATGTGCCACTCTACTCAAGCTTGTGTGACGGATTGAGACCCTGTCTCAAAAAACTAAACAAA T C ZNF91 Ensembl:ENSG00000167232 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909119611 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193761,RMVar_hsa_circ_193762 2726 RMVar_ID_2726 Human_SNP_ID_661816558 A-to-I Human chr19 - 23371124 23371124 23371124 GTTGGTTAGGCTGGTCTTGAGCTCCTGACCTCAGGTGATCTGCCTGCCGTGGCCTCCCAAAGTGC GTTGGTTAGGCTGGTCTTGAGCTCCTGACCTCGGGTGATCTGCCTGCCGTGGCCTCCCAAAGTGC T C ZNF91 Ensembl:ENSG00000167232 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1464832184 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193761,RMVar_hsa_circ_193762 2727 RMVar_ID_2727 Human_SNP_ID_661898581 A-to-I Human chr19 - 23658179 23658179 23658179 TTTTTTTGCATTTTTAGTAGAGACAGGGTTTCACCGTGTTGCCGAGTCTGGTCTCAAACCCCTGA TTTTTTTGCATTTTTAGTAGAGACAGGGTTTCCCCGTGTTGCCGAGTCTGGTCTCAAACCCCTGA T G ZNF675 Ensembl:ENSG00000197372 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1284042163 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13415012,Human_RBP_ID_23789357 RMVar_hsa_circ_193775,RMVar_hsa_circ_79955 2728 RMVar_ID_2728 Human_SNP_ID_661898664 A-to-I Human chr19 - 23658487 23658487 23658487 TTAGTAGAGATGGGGTTTCACCATGTTGGCCAAGCTGGTCTTGAACTCCTGACCTCGTGATCCAT TTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGACCTCGTGATCCAT T C ZNF675 Ensembl:ENSG00000197372 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1434868410 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193775,RMVar_hsa_circ_79955 2729 RMVar_ID_2729 Human_SNP_ID_661898677 A-to-I Human chr19 - 23658535 23658535 23658535 GCTGGGACTATAGGCACATGCCACCATGCCTGACTAATTTTTGTACTTTTAGTAGAGATGGGGTT GCTGGGACTATAGGCACATGCCACCATGCCTGTCTAATTTTTGTACTTTTAGTAGAGATGGGGTT T A ZNF675 Ensembl:ENSG00000197372 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4254446 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193775,RMVar_hsa_circ_79955 2730 RMVar_ID_2730 Human_SNP_ID_661898678 A-to-I Human chr19 - 23658535 23658535 23658535 GCTGGGACTATAGGCACATGCCACCATGCCTGACTAATTTTTGTACTTTTAGTAGAGATGGGGTT GCTGGGACTATAGGCACATGCCACCATGCCTGGCTAATTTTTGTACTTTTAGTAGAGATGGGGTT T C ZNF675 Ensembl:ENSG00000197372 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4254446 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193775,RMVar_hsa_circ_79955 2731 RMVar_ID_2731 Human_SNP_ID_661899599 A-to-I Human chr19 - 23661054 23661054 23661054 GTGGTGGCACACATCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACCCG GTGGTGGCACACATCTGTAATCCCAGCTACTCTGGAGGCTGAGGCAGGAGAATCGCTTGAACCCG T A ZNF675 Ensembl:ENSG00000197372 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs148196860 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193775,RMVar_hsa_circ_79955 2732 RMVar_ID_2732 Human_SNP_ID_661899600 A-to-I Human chr19 - 23661054 23661054 23661054 GTGGTGGCACACATCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACCCG GTGGTGGCACACATCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCG T C ZNF675 Ensembl:ENSG00000197372 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs148196860 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193775,RMVar_hsa_circ_79955 2733 RMVar_ID_2733 Human_SNP_ID_661899738 A-to-I Human chr19 - 23661461 23661461 23661461 GTCTCAAACTCCTGCCCTCAGGTCATTTGCTTACCTTGGCTTCTCAAAGTGCTGGGATTACAGGT GTCTCAAACTCCTGCCCTCAGGTCATTTGCTTTCCTTGGCTTCTCAAAGTGCTGGGATTACAGGT T A ZNF675 Ensembl:ENSG00000197372 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10411860 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193775,RMVar_hsa_circ_79955 2734 RMVar_ID_2734 Human_SNP_ID_661899739 A-to-I Human chr19 - 23661461 23661461 23661461 GTCTCAAACTCCTGCCCTCAGGTCATTTGCTTACCTTGGCTTCTCAAAGTGCTGGGATTACAGGT GTCTCAAACTCCTGCCCTCAGGTCATTTGCTTGCCTTGGCTTCTCAAAGTGCTGGGATTACAGGT T C ZNF675 Ensembl:ENSG00000197372 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10411860 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193775,RMVar_hsa_circ_79955 2735 RMVar_ID_2735 Human_SNP_ID_661899754 A-to-I Human chr19 - 23661528 23661528 23661528 GTGCCACCACACCCGGCTAATTTTGTGTTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGC GTGCCACCACACCCGGCTAATTTTGTGTTTTTGGTAGAGATGGGGTTTCACCATGTTGGCCAGGC T C ZNF675 Ensembl:ENSG00000197372 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs77231873 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193775,RMVar_hsa_circ_79955 2736 RMVar_ID_2736 Human_SNP_ID_661899784 A-to-I Human chr19 - 23661644 23661644 23661644 GCTCTGTAGCCCAGGCTGGGGTGCAGTGCTACAGTCTGGACTCACTGTAACTTTTGCCTCTTGGG GCTCTGTAGCCCAGGCTGGGGTGCAGTGCTACCGTCTGGACTCACTGTAACTTTTGCCTCTTGGG T G ZNF675 Ensembl:ENSG00000197372 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1167663201 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13415092 RMVar_hsa_circ_193775,RMVar_hsa_circ_79955 2737 RMVar_ID_2737 Human_SNP_ID_661904086 A-to-I Human chr19 - 23677489 23677489 23677489 GTTGGCCAGGCTTGTCTCCAACTCCCGACCTCAGGTGATCTGCCCCTCTTGGCCTCCCAAAGTGC GTTGGCCAGGCTTGTCTCCAACTCCCGACCTCGGGTGATCTGCCCCTCTTGGCCTCCCAAAGTGC T C ZNF675 Ensembl:ENSG00000197372 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1336418001 Functional Loss SNV dbSNP153 33..33 33 - - - 2738 RMVar_ID_2738 Human_SNP_ID_662000712 A-to-I Human chr19 - 24002025 24002023 24002025 GAATGAGCGCTTGTGTTAGGCACCAAAAGATGATAAACTATGCCTGGGCAGGGCGAAGCGAGAGG GAATGAGCGCTTGTGTTAGGCACCAAAAGATGGTGAACTATGCCTGGGCAGGGCGAAGCGAGAGG TAT CAC RF02543-023 RNACentral:URS00009843EB rRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs796625187 Functional Loss MNV dbSNP153 33..35 33 - - - Human_RBP_ID_270082,Human_RBP_ID_2573707,Human_RBP_ID_5194207,Human_RBP_ID_9085581,Human_RBP_ID_13547328,Human_RBP_ID_17063354,Human_RBP_ID_17190609,Human_RBP_ID_17695046,Human_RBP_ID_23789433,Human_RBP_ID_24484018,Human_RBP_ID_26466605 2739 RMVar_ID_2739 Human_SNP_ID_662000716 A-to-I Human chr19 - 24002025 24002025 24002025 GAATGAGCGCTTGTGTTAGGCACCAAAAGATGATAAACTATGCCTGGGCAGGGCGAAGCGAGAGG GAATGAGCGCTTGTGTTAGGCACCAAAAGATGGTAAACTATGCCTGGGCAGGGCGAAGCGAGAGG T C RF02543-023 RNACentral:URS00009843EB rRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs78418804 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_270082,Human_RBP_ID_2573707,Human_RBP_ID_5194207,Human_RBP_ID_9085581,Human_RBP_ID_13547328,Human_RBP_ID_17063354,Human_RBP_ID_17190609,Human_RBP_ID_17695046,Human_RBP_ID_23789433,Human_RBP_ID_24484018,Human_RBP_ID_26466605 2740 RMVar_ID_2740 Human_SNP_ID_662015368 A-to-I Human chr19 + 24050349 24050348 24050350 GTCTGGCTGATTTTTGTGTTTTCAGTAGAGACAAGATATCACCCTGTTGGCCAGGCCGATATCAA GTCTGGCTGATTTTTGTGTTTTCAGTAGAGAC__GATATCACCCTGTTGGCCAGGCCGATATCAA CAA C AC092279.1,ZNF254 Ensembl:ENSG00000268362,Ensembl:ENSG00000213096 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474189095 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_3566074,Human_RBP_ID_13415825,Human_RBP_ID_25392952 RMVar_hsa_circ_356302 2741 RMVar_ID_2741 Human_SNP_ID_662019128 A-to-I Human chr19 + 24064620 24064619 24064620 GCAATCTCAGCTCACCACAACCTTCATCTCCCAGGTTCAAGCAATTCTTCAGCCTCAGCCCCCTG GCAATCTCAGCTCACCACAACCTTCATCTCCC_GGTTCAAGCAATTCTTCAGCCTCAGCCCCCTG CA C AC092279.1,ZNF254 Ensembl:ENSG00000268362,Ensembl:ENSG00000213096 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1469793948 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5099346 Human_Splice_Rec_1986270 RMVar_hsa_circ_356302 2742 RMVar_ID_2742 Human_SNP_ID_662019673 A-to-I Human chr19 + 24066779 24066779 24066779 AAAATCAGCCAGGTGTGGTGATTGGTGCCTGTAGTTGCAGCTACTCAGGAGGCTGAGGCAGGATA AAAATCAGCCAGGTGTGGTGATTGGTGCCTGTGGTTGCAGCTACTCAGGAGGCTGAGGCAGGATA A G AC092279.1,ZNF254 Ensembl:ENSG00000268362,Ensembl:ENSG00000213096 lincRNA,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1392214971 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13416527 RMVar_hsa_circ_356302 2743 RMVar_ID_2743 Human_SNP_ID_662020946 A-to-I Human chr19 + 24071821 24071820 24071821 CTTCTACAGGGTTCAGGACGGAAAGGAGAGTTACATCACTTAGGTGATGAACAAAATGATATGTC CTTCTACAGGGTTCAGGACGGAAAGGAGAGTT_CATCACTTAGGTGATGAACAAAATGATATGTC TA T AC092279.1,ZNF254 Ensembl:ENSG00000268362,Ensembl:ENSG00000213096 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1219589129 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_22720453 RMVar_hsa_circ_356302 2744 RMVar_ID_2744 Human_SNP_ID_662020948 A-to-I Human chr19 + 24071835 24071835 24071835 AGGACGGAAAGGAGAGTTACATCACTTAGGTGATGAACAAAATGATATGTCATAATTCCCCTATT AGGACGGAAAGGAGAGTTACATCACTTAGGTGGTGAACAAAATGATATGTCATAATTCCCCTATT A G AC092279.1,ZNF254 Ensembl:ENSG00000268362,Ensembl:ENSG00000213096 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1293936366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22720453 RMVar_hsa_circ_356302 2745 RMVar_ID_2745 Human_SNP_ID_662020999 A-to-I Human chr19 + 24072063 24072063 24072063 AAATTATGACATAATCATTTTGTTTATAACCTAAGTGATGTAACTGTCCTTTTCTACTTGAGCTC AAATTATGACATAATCATTTTGTTTATAACCTTAGTGATGTAACTGTCCTTTTCTACTTGAGCTC A T AC092279.1,ZNF254 Ensembl:ENSG00000268362,Ensembl:ENSG00000213096 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs184012424 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_356302 2746 RMVar_ID_2746 Human_SNP_ID_662025576 A-to-I Human chr19 + 24089944 24089944 24089944 CAGGCATGGTGGCTCATGCCTGTAATCCCTACACTTTGGGAGGCCAAGGAGGGTGGATCACGAAG CAGGCATGGTGGCTCATGCCTGTAATCCCTACGCTTTGGGAGGCCAAGGAGGGTGGATCACGAAG A G ZNF254 Ensembl:ENSG00000213096 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs935652459 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_356302 2747 RMVar_ID_2747 Human_SNP_ID_662025774 A-to-I Human chr19 + 24090586 24090586 24090586 AGCCTCCCAAGTAGCTGGGACTACAGGTGTGCACCACCACACTCAGCTAGTTTCTGTAGTTTTAG AGCCTCCCAAGTAGCTGGGACTACAGGTGTGCGCCACCACACTCAGCTAGTTTCTGTAGTTTTAG A G ZNF254 Ensembl:ENSG00000213096 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1305520329 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_356302 2748 RMVar_ID_2748 Human_SNP_ID_662027895 A-to-I Human chr19 + 24099266 24099266 24099266 TGACCTCATGATCCACCAGCCTCAGCCTCCCAAAGTGCTAGGATAACAGGCATGAGCCACCCTGC TGACCTCATGATCCACCAGCCTCAGCCTCCCAGAGTGCTAGGATAACAGGCATGAGCCACCCTGC A G ZNF254 Ensembl:ENSG00000213096 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1398017787 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_356302 2749 RMVar_ID_2749 Human_SNP_ID_662458040 A-to-I Human chr19 - 27784198 27784198 27784198 GTTGTCTGCGCTTATCTTGAACTCCTGGCCTTAAGTGATCCTCTTTCCTTGGCCTCCTACTGCAC GTTGTCTGCGCTTATCTTGAACTCCTGGCCTTCAGTGATCCTCTTTCCTTGGCCTCCTACTGCAC T G LINC00662 Ensembl:ENSG00000261824 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251725064 Functional Loss SNV dbSNP153 33..33 33 - - - 2750 RMVar_ID_2750 Human_SNP_ID_662464377 A-to-I Human chr19 + 27807826 27807826 27807826 TATCACCAGAATGAGGAAAACAGCGTGGTACTAGCATAAGAACAAACACATAGACCAGTGAAAAA TATCACCAGAATGAGGAAAACAGCGTGGTACTGGCATAAGAACAAACACATAGACCAGTGAAAAA A G AC006504.5 Ensembl:ENSG00000267575 lincRNA intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1195130671 Functional Loss SNV dbSNP153 33..33 33 - - - 2751 RMVar_ID_2751 Human_SNP_ID_662464382 A-to-I Human chr19 + 27807837 27807837 27807837 TGAGGAAAACAGCGTGGTACTAGCATAAGAACAAACACATAGACCAGTGAAAAAGGATAGAGAAC TGAGGAAAACAGCGTGGTACTAGCATAAGAACGAACACATAGACCAGTGAAAAAGGATAGAGAAC A G AC006504.5 Ensembl:ENSG00000267575 lincRNA intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1254220121 Functional Loss SNV dbSNP153 33..33 33 - - - 2752 RMVar_ID_2752 Human_SNP_ID_662464389 A-to-I Human chr19 + 27807886 27807886 27807886 AAAAAGGATAGAGAACCCAGCAACAAATCCACACATTTACAGAAAACTCATTTTTGACAAAGATA AAAAAGGATAGAGAACCCAGCAACAAATCCACGCATTTACAGAAAACTCATTTTTGACAAAGATA A G AC006504.5 Ensembl:ENSG00000267575 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1411779231 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17498582,Human_RBP_ID_27466465 2753 RMVar_ID_2753 Human_SNP_ID_662464415 A-to-I Human chr19 + 27807990 27807990 27807990 AATGGTGCTGGGGAAACTGGATATCCATATGCAAAAGAATAAAACTGGATTCCTATCTCCCACCA AATGGTGCTGGGGAAACTGGATATCCATATGCGAAAGAATAAAACTGGATTCCTATCTCCCACCA A G AC006504.5 Ensembl:ENSG00000267575 lincRNA intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs746416204 Functional Loss SNV dbSNP153 33..33 33 - - - 2754 RMVar_ID_2754 Human_SNP_ID_662464951 A-to-I Human chr19 + 27809975 27809975 27809975 TATTCTGCTTATCAATCGCTTGTCGGATGTGTAGCTTGCACATATTTTCTCTCTTATCTCTTTTT TATTCTGCTTATCAATCGCTTGTCGGATGTGTGGCTTGCACATATTTTCTCTCTTATCTCTTTTT A G AC006504.5 Ensembl:ENSG00000267575 lincRNA intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1044725289 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6735266 2755 RMVar_ID_2755 Human_SNP_ID_662972220 A-to-I Human chr19 - 29699233 29699233 29699233 TCAATCTCCTTACCTCGTGATCTGCCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG TCAATCTCCTTACCTCGTGATCTGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG T C C19orf12 Ensembl:ENSG00000131943 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1443217621 Functional Loss SNV dbSNP153 33..33 33 - - - 2756 RMVar_ID_2756 Human_SNP_ID_662972828 A-to-I Human chr19 - 29700983 29700983 29700983 GGAGGCCAAAGTGGGAGGATCGCTTGAGGCCAAGAGTTTGAAACTAGCCTGGGCAATATAGTGAG GGAGGCCAAAGTGGGAGGATCGCTTGAGGCCAGGAGTTTGAAACTAGCCTGGGCAATATAGTGAG T C C19orf12 Ensembl:ENSG00000131943 Protein coding 3'UTR GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1405152215 Functional Loss SNV dbSNP153 33..33 33 - - - 2757 RMVar_ID_2757 Human_SNP_ID_662974325 A-to-I Human chr19 - 29705716 29705716 29705716 GCCCAGCAGTTCGAGACCGGACTGGGCAACATAATGAGACCCCGTCTCTACGAAAAATAATAAAA GCCCAGCAGTTCGAGACCGGACTGGGCAACATTATGAGACCCCGTCTCTACGAAAAATAATAAAA T A C19orf12 Ensembl:ENSG00000131943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1015468239 Functional Loss SNV dbSNP153 33..33 33 - - - 2758 RMVar_ID_2758 Human_SNP_ID_662974802 A-to-I Human chr19 - 29707970 29707970 29707970 CTACTCGGGAGGCTGAGGCAGGAGAATCGCTTAAACCCGGGAGGCAAAGATTGCAGTGAGCCAAG CTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGGGAGGCAAAGATTGCAGTGAGCCAAG T C C19orf12 Ensembl:ENSG00000131943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1568332017 Functional Loss SNV dbSNP153 33..33 33 - - - 2759 RMVar_ID_2759 Human_SNP_ID_662975877 A-to-I Human chr19 - 29712162 29712162 29712162 TGACCTCGTGATCTGCCCACCTCGGCTTCCCAAAGTGCTGGGATTACAAGCGTGAGCCACCGTGG TGACCTCGTGATCTGCCCACCTCGGCTTCCCACAGTGCTGGGATTACAAGCGTGAGCCACCGTGG T G C19orf12 Ensembl:ENSG00000131943 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs996047357 Functional Loss SNV dbSNP153 33..33 33 - - - 2760 RMVar_ID_2760 Human_SNP_ID_662975900 A-to-I Human chr19 - 29712238 29712238 29712238 TGACACCTGGCTAATTTTTGTATTTTTTTAGTAGAGATGGGTTTTCACCATGTTGGCCAGGATAG TGACACCTGGCTAATTTTTGTATTTTTTTAGTGGAGATGGGTTTTCACCATGTTGGCCAGGATAG T C C19orf12 Ensembl:ENSG00000131943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1210539023 Functional Loss SNV dbSNP153 33..33 33 - - - 2761 RMVar_ID_2761 Human_SNP_ID_662975917 A-to-I Human chr19 - 29712343 29712343 29712343 GGAGTGCAGTGGTGTGATCTCAGCTCACTGCAACCTCCACCTCCCGGGTTCAAGTGGTTCTCCTG GGAGTGCAGTGGTGTGATCTCAGCTCACTGCACCCTCCACCTCCCGGGTTCAAGTGGTTCTCCTG T G C19orf12 Ensembl:ENSG00000131943 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1298954977 Functional Loss SNV dbSNP153 33..33 33 - - - 2762 RMVar_ID_2762 Human_SNP_ID_663039730 A-to-I Human chr19 + 29943145 29943145 29943145 TTTAAACATTAAAAAAAAAAGAGAGTCTCACTATGTTGCCCAGGCTAATCTCGAACTTCTGGCCT TTTAAACATTAAAAAAAAAAGAGAGTCTCACTGTGTTGCCCAGGCTAATCTCGAACTTCTGGCCT A G URI1 Ensembl:ENSG00000105176 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1024559967 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80027,RMVar_hsa_circ_193818 2763 RMVar_ID_2763 Human_SNP_ID_165559942 A-to-I Human chr3 - 180773576 180773576 180773576 TGATATAAAGATTTTAAATGCACAGAGAGCAGAATACAAAGCAGCCATAGTTCACAATGTTGATT TGATATAAAGATTTTAAATGCACAGAGAGCAGGATACAAAGCAGCCATAGTTCACAATGTTGATT T C CCDC39,AC108734.3,AC108734.4 Ensembl:ENSG00000145075,Ensembl:ENSG00000242068,Ensembl:ENSG00000285336 lincRNA,Pseudogene,lincRNA intron,exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1377168484 Functional Loss SNV dbSNP153 33..33 33 - - - 2764 RMVar_ID_2764 Human_SNP_ID_165559945 A-to-I Human chr3 - 180773598 180773598 180773598 TTAGAAGACTTGATTGTAATTTTGATATAAAGATTTTAAATGCACAGAGAGCAGAATACAAAGCA TTAGAAGACTTGATTGTAATTTTGATATAAAGGTTTTAAATGCACAGAGAGCAGAATACAAAGCA T C CCDC39,AC108734.3,AC108734.4 Ensembl:ENSG00000145075,Ensembl:ENSG00000242068,Ensembl:ENSG00000285336 lincRNA,Pseudogene,lincRNA intron,exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1023212705 Functional Loss SNV dbSNP153 33..33 33 - - - 2765 RMVar_ID_2765 Human_SNP_ID_165594691 A-to-I Human chr3 + 180916573 180916573 180916573 GGGACAACAGGCATGTGCTAACATGGCCGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTTA GGGACAACAGGCATGTGCTAACATGGCCGGCTCATTTTTGTATTTTTAGTAGAGACGGGGTTTTA A C FXR1 Ensembl:ENSG00000114416 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1243224758 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14739065 RMVar_hsa_circ_3776,RMVar_hsa_circ_269031 2766 RMVar_ID_2766 Human_SNP_ID_165595011 A-to-I Human chr3 + 180917732 180917732 180917732 GCACTTTGTGGGGCTGAGGTGCGTGGATCACGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACAT GCACTTTGTGGGGCTGAGGTGCGTGGATCACGGGGTCAGGAGTTCGAGACCAGCCTGGCCAACAT A G FXR1 Ensembl:ENSG00000114416 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054595884 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3776,RMVar_hsa_circ_269031 2767 RMVar_ID_2767 Human_SNP_ID_165595014 A-to-I Human chr3 + 180917737 180917737 180917737 TTGTGGGGCTGAGGTGCGTGGATCACGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATAGAGA TTGTGGGGCTGAGGTGCGTGGATCACGAGGTCCGGAGTTCGAGACCAGCCTGGCCAACATAGAGA A C FXR1 Ensembl:ENSG00000114416 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355418768 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3776,RMVar_hsa_circ_269031 2768 RMVar_ID_2768 Human_SNP_ID_165595015 A-to-I Human chr3 + 180917737 180917737 180917737 TTGTGGGGCTGAGGTGCGTGGATCACGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATAGAGA TTGTGGGGCTGAGGTGCGTGGATCACGAGGTCTGGAGTTCGAGACCAGCCTGGCCAACATAGAGA A T FXR1 Ensembl:ENSG00000114416 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355418768 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3776,RMVar_hsa_circ_269031 2769 RMVar_ID_2769 Human_SNP_ID_165595930 A-to-I Human chr3 + 180920779 180920779 180920779 GTGATCTGCCTGCCTCAGCCTCCCAAAGTGCTAGGATTACAGGTGTGAGCCACCATGCCCGGCCC GTGATCTGCCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCATGCCCGGCCC A G FXR1 Ensembl:ENSG00000114416 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs937551720 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3776,RMVar_hsa_circ_269031 2770 RMVar_ID_2770 Human_SNP_ID_165597102 A-to-I Human chr3 + 180925250 180925250 180925250 GGGCATGGTGGCACGTGCCTCTAGTCCCAGCTACTCGGAAGGCTAAGGCAGAAGAATCGCTTGAA GGGCATGGTGGCACGTGCCTCTAGTCCCAGCTCCTCGGAAGGCTAAGGCAGAAGAATCGCTTGAA A C FXR1 Ensembl:ENSG00000114416 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1238496572 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3776,RMVar_hsa_circ_269031 2771 RMVar_ID_2771 Human_SNP_ID_165598740 A-to-I Human chr3 + 180930870 180930870 180930870 CAGCCTGGCCCACATGGCAAAACTCTGTCTCTACTAAAAATACAAAAAAATTAGCTGGGTGTGGT CAGCCTGGCCCACATGGCAAAACTCTGTCTCTGCTAAAAATACAAAAAAATTAGCTGGGTGTGGT A G FXR1 Ensembl:ENSG00000114416 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1382053506 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3776,RMVar_hsa_circ_269031 2772 RMVar_ID_2772 Human_SNP_ID_165603230 A-to-I Human chr3 + 180947056 180947050 180947056 GAATATGACTTGTTTTTTTGTGGATAGTTTTTATTTTGTTTTTTTTGAGATGGAGTTTTGCTCTA GAATATGACTTGTTTTTTTGTGGATAG______TTTTGTTTTTTTTGAGATGGAGTTTTGCTCTA GTTTTTA G FXR1 Ensembl:ENSG00000114416 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1188817620 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_2769877,Human_RBP_ID_7164327,Human_RBP_ID_14739976 RMVar_hsa_circ_71561,RMVar_hsa_circ_1285,RMVar_hsa_circ_275326,RMVar_hsa_circ_269031,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_223015,RMVar_hsa_circ_223016,RMVar_hsa_circ_116788,RMVar_hsa_circ_223017,RMVar_hsa_circ_31638,RMVar_hsa_circ_56219,RMVar_hsa_circ_223018 2773 RMVar_ID_2773 Human_SNP_ID_165603231 A-to-I Human chr3 + 180947056 180947051 180947056 GAATATGACTTGTTTTTTTGTGGATAGTTTTTATTTTGTTTTTTTTGAGATGGAGTTTTGCTCTA GAATATGACTTGTTTTTTTGTGGATAGT_____TTTTGTTTTTTTTGAGATGGAGTTTTGCTCTA TTTTTA T FXR1 Ensembl:ENSG00000114416 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1490863944 Functional Loss DEL dbSNP153 29..33 33 - - - Human_RBP_ID_2769877,Human_RBP_ID_7164327,Human_RBP_ID_14739976 RMVar_hsa_circ_71561,RMVar_hsa_circ_1285,RMVar_hsa_circ_275326,RMVar_hsa_circ_269031,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_223015,RMVar_hsa_circ_223016,RMVar_hsa_circ_116788,RMVar_hsa_circ_223017,RMVar_hsa_circ_31638,RMVar_hsa_circ_56219,RMVar_hsa_circ_223018 2774 RMVar_ID_2774 Human_SNP_ID_165603232 A-to-I Human chr3 + 180947056 180947056 180947056 GAATATGACTTGTTTTTTTGTGGATAGTTTTTATTTTGTTTTTTTTGAGATGGAGTTTTGCTCTA GAATATGACTTGTTTTTTTGTGGATAGTTTTTGTTTTGTTTTTTTTGAGATGGAGTTTTGCTCTA A G FXR1 Ensembl:ENSG00000114416 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1016947399 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2769877,Human_RBP_ID_7164327,Human_RBP_ID_14739976 RMVar_hsa_circ_71561,RMVar_hsa_circ_1285,RMVar_hsa_circ_275326,RMVar_hsa_circ_269031,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_223015,RMVar_hsa_circ_223016,RMVar_hsa_circ_116788,RMVar_hsa_circ_223017,RMVar_hsa_circ_31638,RMVar_hsa_circ_56219,RMVar_hsa_circ_223018 2775 RMVar_ID_2775 Human_SNP_ID_165603233 A-to-I Human chr3 + 180947056 180947056 180947056 GAATATGACTTGTTTTTTTGTGGATAGTTTTTATTTTGTTTTTTTTGAGATGGAGTTTTGCTCTA GAATATGACTTGTTTTTTTGTGGATAGTTTTTTTTTTGTTTTTTTTGAGATGGAGTTTTGCTCTA A T FXR1 Ensembl:ENSG00000114416 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1016947399 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2769877,Human_RBP_ID_7164327,Human_RBP_ID_14739976 RMVar_hsa_circ_71561,RMVar_hsa_circ_1285,RMVar_hsa_circ_275326,RMVar_hsa_circ_269031,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_223015,RMVar_hsa_circ_223016,RMVar_hsa_circ_116788,RMVar_hsa_circ_223017,RMVar_hsa_circ_31638,RMVar_hsa_circ_56219,RMVar_hsa_circ_223018 2776 RMVar_ID_2776 Human_SNP_ID_165603845 A-to-I Human chr3 + 180949594 180949594 180949594 TTTAGTAGAGGTGGGGTTTTGCCATGTTGGCCAGGCTGGTCTCGAGCTCCTGGGCTCAAGTGATT TTTAGTAGAGGTGGGGTTTTGCCATGTTGGCCGGGCTGGTCTCGAGCTCCTGGGCTCAAGTGATT A G FXR1 Ensembl:ENSG00000114416 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs565981706 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71561,RMVar_hsa_circ_1285,RMVar_hsa_circ_275326,RMVar_hsa_circ_335471,RMVar_hsa_circ_347606,RMVar_hsa_circ_267648,RMVar_hsa_circ_268969,RMVar_hsa_circ_223016,RMVar_hsa_circ_116788,RMVar_hsa_circ_223017,RMVar_hsa_circ_56219,RMVar_hsa_circ_223021,RMVar_hsa_circ_291985,RMVar_hsa_circ_364362,RMVar_hsa_circ_326172,RMVar_hsa_circ_12433,RMVar_hsa_circ_47491,RMVar_hsa_circ_31000 2777 RMVar_ID_2777 Human_SNP_ID_165603862 A-to-I Human chr3 + 180949658 180949658 180949658 TGCCCGCCTCAGCCTCTCAAAGTGCTGGGATTACAGGCATGAGCCACCGAACCTGGCCCCCATTT TGCCCGCCTCAGCCTCTCAAAGTGCTGGGATTGCAGGCATGAGCCACCGAACCTGGCCCCCATTT A G FXR1 Ensembl:ENSG00000114416 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1366359325 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71561,RMVar_hsa_circ_1285,RMVar_hsa_circ_275326,RMVar_hsa_circ_335471,RMVar_hsa_circ_347606,RMVar_hsa_circ_267648,RMVar_hsa_circ_268969,RMVar_hsa_circ_223016,RMVar_hsa_circ_116788,RMVar_hsa_circ_223017,RMVar_hsa_circ_56219,RMVar_hsa_circ_223021,RMVar_hsa_circ_291985,RMVar_hsa_circ_364362,RMVar_hsa_circ_326172,RMVar_hsa_circ_12433,RMVar_hsa_circ_47491,RMVar_hsa_circ_31000 2778 RMVar_ID_2778 Human_SNP_ID_165604198 A-to-I Human chr3 + 180950955 180950955 180950955 CATTTTGTGGCCGCGTGTGGTAGCTCATGCCTATAATCCCAGCACTTTGGGAGGCTGAAGTGGGA CATTTTGTGGCCGCGTGTGGTAGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAAGTGGGA A G FXR1 Ensembl:ENSG00000114416 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1180190557 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71561,RMVar_hsa_circ_1285,RMVar_hsa_circ_275326,RMVar_hsa_circ_335471,RMVar_hsa_circ_347606,RMVar_hsa_circ_267648,RMVar_hsa_circ_268969,RMVar_hsa_circ_223016,RMVar_hsa_circ_116788,RMVar_hsa_circ_223017,RMVar_hsa_circ_56219,RMVar_hsa_circ_223021,RMVar_hsa_circ_291985,RMVar_hsa_circ_364362,RMVar_hsa_circ_326172,RMVar_hsa_circ_12433,RMVar_hsa_circ_47491,RMVar_hsa_circ_31000 2779 RMVar_ID_2779 Human_SNP_ID_165604510 A-to-I Human chr3 + 180952232 180952232 180952232 CACCTGCCTCAGCCTTCCAAAGTGCCGGGACTATAGGCGTGAGCCACCGTGCCTGGCCTGGAGTT CACCTGCCTCAGCCTTCCAAAGTGCCGGGACTGTAGGCGTGAGCCACCGTGCCTGGCCTGGAGTT A G FXR1 Ensembl:ENSG00000114416 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1483508721 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71561,RMVar_hsa_circ_1285,RMVar_hsa_circ_275326,RMVar_hsa_circ_335471,RMVar_hsa_circ_267648,RMVar_hsa_circ_268969,RMVar_hsa_circ_223016,RMVar_hsa_circ_56219,RMVar_hsa_circ_364362,RMVar_hsa_circ_326172,RMVar_hsa_circ_31000,RMVar_hsa_circ_344188 2780 RMVar_ID_2780 Human_SNP_ID_165606864 A-to-I Human chr3 + 180961217 180961217 180961217 AAAGTAATAGCTGGTTGTGGTGACACGCATCTATAGTCCCAGCTACTCTGGAGGCTGAGACAGGA AAAGTAATAGCTGGTTGTGGTGACACGCATCTGTAGTCCCAGCTACTCTGGAGGCTGAGACAGGA A G FXR1 Ensembl:ENSG00000114416 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs983250089 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71561,RMVar_hsa_circ_1285,RMVar_hsa_circ_275326,RMVar_hsa_circ_267648,RMVar_hsa_circ_268969,RMVar_hsa_circ_326172,RMVar_hsa_circ_71478,RMVar_hsa_circ_31000,RMVar_hsa_circ_83128,RMVar_hsa_circ_223022,RMVar_hsa_circ_351430 2781 RMVar_ID_2781 Human_SNP_ID_165612908 A-to-I Human chr3 - 180984241 180984241 180984241 GTATGATGGAAATTAGCTTAAGCTGTTTAAGTAGGGACTCTTCTTATTCGGTGGAAAGGCTGTTC GTATGATGGAAATTAGCTTAAGCTGTTTAAGTCGGGACTCTTCTTATTCGGTGGAAAGGCTGTTC T G DNAJC19 Ensembl:ENSG00000205981 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1206511800 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_595892,Human_RBP_ID_2770078,Human_RBP_ID_17402648,Human_RBP_ID_23987643 Human_miRNA_ID_583131 RMVar_hsa_circ_223023 2782 RMVar_ID_2782 Human_SNP_ID_166005452 A-to-I Human chr3 - 182642312 182642312 182642312 AAAAAAAAAATTGGCTGGGCGTGGTGGTGGGCACCTGTGGTCCCAGCTGCTCGGGAGGCTGAGGC AAAAAAAAAATTGGCTGGGCGTGGTGGTGGGCGCCTGTGGTCCCAGCTGCTCGGGAGGCTGAGGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1316073935 Functional Loss SNV dbSNP153 33..33 33 - - - 2783 RMVar_ID_2783 Human_SNP_ID_166048491 A-to-I Human chr3 + 182820502 182820502 182820502 GCCCAGGAGTTTGCGACCAGTGTGGGCAACATAATGAGACCTTGTCTCTGCAAAAAATCAAAAAA GCCCAGGAGTTTGCGACCAGTGTGGGCAACATGATGAGACCTTGTCTCTGCAAAAAATCAAAAAA A G ATP11B Ensembl:ENSG00000058063 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1004042593 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_223045,RMVar_hsa_circ_127978,RMVar_hsa_circ_223043,RMVar_hsa_circ_106000,RMVar_hsa_circ_310405,RMVar_hsa_circ_325789,RMVar_hsa_circ_275153,RMVar_hsa_circ_59456,RMVar_hsa_circ_64108,RMVar_hsa_circ_223046,RMVar_hsa_circ_223047 2784 RMVar_ID_2784 Human_SNP_ID_166048710 A-to-I Human chr3 + 182821381 182821381 182821381 CACCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGTATGAGCCACTGCACCCGGCCATAGATT CACCCACCTCGGCCTCCCAAAGTGCTGGGATTGCAGGTATGAGCCACTGCACCCGGCCATAGATT A G ATP11B Ensembl:ENSG00000058063 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs937868825 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_223045,RMVar_hsa_circ_127978,RMVar_hsa_circ_223043,RMVar_hsa_circ_106000,RMVar_hsa_circ_310405,RMVar_hsa_circ_325789,RMVar_hsa_circ_275153,RMVar_hsa_circ_59456,RMVar_hsa_circ_64108,RMVar_hsa_circ_223046,RMVar_hsa_circ_223047 2785 RMVar_ID_2785 Human_SNP_ID_166048711 A-to-I Human chr3 + 182821383 182821383 182821383 CCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGTATGAGCCACTGCACCCGGCCATAGATTGG CCCACCTCGGCCTCCCAAAGTGCTGGGATTACGGGTATGAGCCACTGCACCCGGCCATAGATTGG A G ATP11B Ensembl:ENSG00000058063 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1371014163 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_223045,RMVar_hsa_circ_127978,RMVar_hsa_circ_223043,RMVar_hsa_circ_106000,RMVar_hsa_circ_310405,RMVar_hsa_circ_325789,RMVar_hsa_circ_275153,RMVar_hsa_circ_59456,RMVar_hsa_circ_64108,RMVar_hsa_circ_223046,RMVar_hsa_circ_223047 2786 RMVar_ID_2786 Human_SNP_ID_166051456 A-to-I Human chr3 + 182833452 182833452 182833452 GGCTCAGGTGATCCTTCCACCTCAGCCTACCAAATAGCTGGGACTACAGTTGCGTGCCACCACAC GGCTCAGGTGATCCTTCCACCTCAGCCTACCAGATAGCTGGGACTACAGTTGCGTGCCACCACAC A G ATP11B Ensembl:ENSG00000058063 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs535732201 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127978,RMVar_hsa_circ_223043,RMVar_hsa_circ_106000,RMVar_hsa_circ_310405,RMVar_hsa_circ_325789,RMVar_hsa_circ_59456,RMVar_hsa_circ_64108,RMVar_hsa_circ_223046,RMVar_hsa_circ_223047,RMVar_hsa_circ_25640,RMVar_hsa_circ_357816,RMVar_hsa_circ_316606,RMVar_hsa_circ_223049,RMVar_hsa_circ_74639,RMVar_hsa_circ_367085 2787 RMVar_ID_2787 Human_SNP_ID_166063082 A-to-I Human chr3 + 182881180 182881180 182881180 TAATTAGGCCGGGCGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGGGGTTGAGGCAGGCAG TAATTAGGCCGGGCGTGGTGGCTCACGCCTGTTATCCCAGCACTTTGGGGGGTTGAGGCAGGCAG A T ATP11B Ensembl:ENSG00000058063 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs533607814 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_440,RMVar_hsa_circ_127978,RMVar_hsa_circ_310405,RMVar_hsa_circ_59456,RMVar_hsa_circ_223047,RMVar_hsa_circ_367085,RMVar_hsa_circ_18700,RMVar_hsa_circ_41794,RMVar_hsa_circ_18433,RMVar_hsa_circ_348125,RMVar_hsa_circ_2549,RMVar_hsa_circ_223055,RMVar_hsa_circ_9865,RMVar_hsa_circ_10461,RMVar_hsa_circ_269486,RMVar_hsa_circ_61657,RMVar_hsa_circ_101522,RMVar_hsa_circ_223060,RMVar_hsa_circ_5425,RMVar_hsa_circ_35192,RMVar_hsa_circ_4221,RMVar_hsa_circ_223061,RMVar_hsa_circ_223066,RMVar_hsa_circ_58107,RMVar_hsa_circ_316968,RMVar_hsa_circ_296262,RMVar_hsa_circ_223063,RMVar_hsa_circ_73114,RMVar_hsa_circ_223065,RMVar_hsa_circ_125829 2788 RMVar_ID_2788 Human_SNP_ID_166066245 A-to-I Human chr3 + 182894420 182894420 182894420 GTTGGTAAGGCTGGTCACGAACTCCCAACCTCAGGTGATCCGCCTGCCTCGGCCTCCCAAAGTGC GTTGGTAAGGCTGGTCACGAACTCCCAACCTCGGGTGATCCGCCTGCCTCGGCCTCCCAAAGTGC A G ATP11B Ensembl:ENSG00000058063 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1420399819 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_440,RMVar_hsa_circ_127978,RMVar_hsa_circ_310405,RMVar_hsa_circ_223047,RMVar_hsa_circ_367085,RMVar_hsa_circ_41794,RMVar_hsa_circ_18433,RMVar_hsa_circ_348125,RMVar_hsa_circ_223055,RMVar_hsa_circ_9865,RMVar_hsa_circ_269486,RMVar_hsa_circ_101522,RMVar_hsa_circ_223060,RMVar_hsa_circ_4221,RMVar_hsa_circ_223061,RMVar_hsa_circ_58107,RMVar_hsa_circ_316968,RMVar_hsa_circ_223063,RMVar_hsa_circ_73114,RMVar_hsa_circ_223068,RMVar_hsa_circ_275254,RMVar_hsa_circ_313983,RMVar_hsa_circ_45710,RMVar_hsa_circ_223067,RMVar_hsa_circ_25868,RMVar_hsa_circ_340968,RMVar_hsa_circ_223073 2789 RMVar_ID_2789 Human_SNP_ID_166075882 A-to-I Human chr3 - 182932259 182932259 182932259 TAAAATACTTTCTCTATAGATTTGCCTATCTTAGATATTTCACATAAATGGAATCATTCAATATG TAAAATACTTTCTCTATAGATTTGCCTATCTTCGATATTTCACATAAATGGAATCATTCAATATG T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1029109973 Functional Loss SNV dbSNP153 33..33 33 - - - 2790 RMVar_ID_2790 Human_SNP_ID_166077103 A-to-I Human chr3 - 182937432 182937432 182937432 GCACACATTGTACTATTCCATTTGTATGACACATCCAGAATAGGCAAATCTATAGAGAGAAAGAT GCACACATTGTACTATTCCATTTGTATGACACGTCCAGAATAGGCAAATCTATAGAGAGAAAGAT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1228600829 Functional Loss SNV dbSNP153 33..33 33 - - - 2791 RMVar_ID_2791 Human_SNP_ID_166077104 A-to-I Human chr3 - 182937439 182937439 182937439 CAAAAGGGCACACATTGTACTATTCCATTTGTATGACACATCCAGAATAGGCAAATCTATAGAGA CAAAAGGGCACACATTGTACTATTCCATTTGTGTGACACATCCAGAATAGGCAAATCTATAGAGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1224070148 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20866147 2792 RMVar_ID_2792 Human_SNP_ID_166087096 A-to-I Human chr3 - 182977883 182977883 182977883 GGTGCCCGCCAACATACCCGGCTGATTTTTGTATTTTTAGTAGAGACGAGGTTTCACTATGTTGA GGTGCCCGCCAACATACCCGGCTGATTTTTGTGTTTTTAGTAGAGACGAGGTTTCACTATGTTGA T C DCUN1D1 Ensembl:ENSG00000043093 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs902367145 Functional Loss SNV dbSNP153 33..33 33 - - - 2793 RMVar_ID_2793 Human_SNP_ID_166087131 A-to-I Human chr3 - 182977993 182977993 182977993 CTCTGTTGCCCAGGCTGGAGTGCAGTGGTGCAATCTTGGCTCACTGCAACCCGTGCCTCCTGGGT CTCTGTTGCCCAGGCTGGAGTGCAGTGGTGCAGTCTTGGCTCACTGCAACCCGTGCCTCCTGGGT T C DCUN1D1 Ensembl:ENSG00000043093 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs558710039 Functional Loss SNV dbSNP153 33..33 33 - - - 2794 RMVar_ID_2794 Human_SNP_ID_166098541 A-to-I Human chr3 - 183026181 183026181 183026181 AAAAAATTAGCCGGGCGTGGTGGCACGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGTGAGGGG AAAAAATTAGCCGGGCGTGGTGGCACGCCTGTGGTCCCAGCTACTTGGGAGGCTGAGGTGAGGGG T C MCCC1 Ensembl:ENSG00000078070 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs772224992 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17701,RMVar_hsa_circ_308185,RMVar_hsa_circ_223079,RMVar_hsa_circ_99891,RMVar_hsa_circ_343432,RMVar_hsa_circ_64575,RMVar_hsa_circ_62079,RMVar_hsa_circ_55109,RMVar_hsa_circ_7265,RMVar_hsa_circ_223082,RMVar_hsa_circ_354476,RMVar_hsa_circ_27665,RMVar_hsa_circ_115816,RMVar_hsa_circ_366611,RMVar_hsa_circ_63689,RMVar_hsa_circ_36017,RMVar_hsa_circ_223083,RMVar_hsa_circ_223084,RMVar_hsa_circ_68897 2795 RMVar_ID_2795 Human_SNP_ID_166098643 A-to-I Human chr3 - 183026623 183026623 183026623 TCACTGCAACCTCCACCTCGCAGGTTCAAGCTATTCTCCTACCTCAGCCCCCTGAGTAGCTGGGA TCACTGCAACCTCCACCTCGCAGGTTCAAGCTGTTCTCCTACCTCAGCCCCCTGAGTAGCTGGGA T C MCCC1 Ensembl:ENSG00000078070 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1411857197 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25718680 RMVar_hsa_circ_17701,RMVar_hsa_circ_308185,RMVar_hsa_circ_223079,RMVar_hsa_circ_99891,RMVar_hsa_circ_343432,RMVar_hsa_circ_64575,RMVar_hsa_circ_62079,RMVar_hsa_circ_55109,RMVar_hsa_circ_7265,RMVar_hsa_circ_223082,RMVar_hsa_circ_354476,RMVar_hsa_circ_27665,RMVar_hsa_circ_115816,RMVar_hsa_circ_366611,RMVar_hsa_circ_63689,RMVar_hsa_circ_36017,RMVar_hsa_circ_223083,RMVar_hsa_circ_223084,RMVar_hsa_circ_68897 2796 RMVar_ID_2796 Human_SNP_ID_166100479 A-to-I Human chr3 - 183034453 183034453 183034453 GACGTGTGTTTTTTTGTTTTTTTTTTTTTTTGAGACGGAGTCTTGCTCTGTCGCCCAGGCTGGAT GACGTGTGTTTTTTTGTTTTTTTTTTTTTTTGTGACGGAGTCTTGCTCTGTCGCCCAGGCTGGAT T A MCCC1 Ensembl:ENSG00000078070 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1231707793 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_308185,RMVar_hsa_circ_64575,RMVar_hsa_circ_62079,RMVar_hsa_circ_55059,RMVar_hsa_circ_55109,RMVar_hsa_circ_7265,RMVar_hsa_circ_223082,RMVar_hsa_circ_354476,RMVar_hsa_circ_27665,RMVar_hsa_circ_115816,RMVar_hsa_circ_366611,RMVar_hsa_circ_223083,RMVar_hsa_circ_223084,RMVar_hsa_circ_68897,RMVar_hsa_circ_290587,RMVar_hsa_circ_336610,RMVar_hsa_circ_73887,RMVar_hsa_circ_223085,RMVar_hsa_circ_41693,RMVar_hsa_circ_54092,RMVar_hsa_circ_223086 2797 RMVar_ID_2797 Human_SNP_ID_166100689 A-to-I Human chr3 - 183035045 183035045 183035045 GCCAGGCGCGGTGGCTCATGCCTGTAATCCCAACACTTTGAGAGGCCCAGGGCGGGTGGATCACT GCCAGGCGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGAGAGGCCCAGGGCGGGTGGATCACT T C MCCC1 Ensembl:ENSG00000078070 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs891577056 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_308185,RMVar_hsa_circ_64575,RMVar_hsa_circ_62079,RMVar_hsa_circ_55059,RMVar_hsa_circ_55109,RMVar_hsa_circ_7265,RMVar_hsa_circ_223082,RMVar_hsa_circ_354476,RMVar_hsa_circ_27665,RMVar_hsa_circ_115816,RMVar_hsa_circ_366611,RMVar_hsa_circ_223083,RMVar_hsa_circ_223084,RMVar_hsa_circ_68897,RMVar_hsa_circ_290587,RMVar_hsa_circ_336610,RMVar_hsa_circ_73887,RMVar_hsa_circ_223085,RMVar_hsa_circ_41693,RMVar_hsa_circ_54092,RMVar_hsa_circ_223086 2798 RMVar_ID_2798 Human_SNP_ID_166102768 A-to-I Human chr3 - 183043203 183043203 183043203 TCACTGCAACCTCTACCTCCCGGCTTCAAGCAATTCTCCTGCCTCAGCCTCCCGTGTAGCTGGGA TCACTGCAACCTCTACCTCCCGGCTTCAAGCAGTTCTCCTGCCTCAGCCTCCCGTGTAGCTGGGA T C MCCC1 Ensembl:ENSG00000078070 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1317818483 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64575,RMVar_hsa_circ_62079,RMVar_hsa_circ_7374,RMVar_hsa_circ_7265,RMVar_hsa_circ_27665,RMVar_hsa_circ_115816,RMVar_hsa_circ_223083,RMVar_hsa_circ_223084,RMVar_hsa_circ_68897,RMVar_hsa_circ_73887,RMVar_hsa_circ_41693,RMVar_hsa_circ_54092,RMVar_hsa_circ_364031,RMVar_hsa_circ_24668,RMVar_hsa_circ_223087,RMVar_hsa_circ_35109,RMVar_hsa_circ_298979,RMVar_hsa_circ_353530 2799 RMVar_ID_2799 Human_SNP_ID_166112741 A-to-I Human chr3 - 183087664 183087664 183087664 TGGGGTTTCACTGTGTTAGCCAGGACGGTCTCAATCTCCTGACCTCATGATCCGCCCGCCTTGGC TGGGGTTTCACTGTGTTAGCCAGGACGGTCTCGATCTCCTGACCTCATGATCCGCCCGCCTTGGC T C MCCC1 Ensembl:ENSG00000078070 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs980638026 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_223092,RMVar_hsa_circ_365888,RMVar_hsa_circ_223096,RMVar_hsa_circ_293363,RMVar_hsa_circ_333240,RMVar_hsa_circ_223095,RMVar_hsa_circ_265759,RMVar_hsa_circ_223097,RMVar_hsa_circ_31448,RMVar_hsa_circ_276935,RMVar_hsa_circ_293717,RMVar_hsa_circ_223098 2800 RMVar_ID_2800 Human_SNP_ID_166112786 A-to-I Human chr3 - 183087810 183087810 183087810 GCTGGAGTTCAGTGGCGCAATCTCGGCTCACTACAAGCTCCGCCTCCCTGTTCACGCCATTCTCC GCTGGAGTTCAGTGGCGCAATCTCGGCTCACTGCAAGCTCCGCCTCCCTGTTCACGCCATTCTCC T C MCCC1 Ensembl:ENSG00000078070 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1207570530 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_223092,RMVar_hsa_circ_365888,RMVar_hsa_circ_223096,RMVar_hsa_circ_293363,RMVar_hsa_circ_333240,RMVar_hsa_circ_223095,RMVar_hsa_circ_265759,RMVar_hsa_circ_223097,RMVar_hsa_circ_31448,RMVar_hsa_circ_276935,RMVar_hsa_circ_293717,RMVar_hsa_circ_223098 2801 RMVar_ID_2801 Human_SNP_ID_166112792 A-to-I Human chr3 - 183087823 183087823 183087823 CCCTGTTGCCCAGGCTGGAGTTCAGTGGCGCAATCTCGGCTCACTACAAGCTCCGCCTCCCTGTT CCCTGTTGCCCAGGCTGGAGTTCAGTGGCGCAGTCTCGGCTCACTACAAGCTCCGCCTCCCTGTT T C MCCC1 Ensembl:ENSG00000078070 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1396243605 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_223092,RMVar_hsa_circ_365888,RMVar_hsa_circ_223096,RMVar_hsa_circ_293363,RMVar_hsa_circ_333240,RMVar_hsa_circ_223095,RMVar_hsa_circ_265759,RMVar_hsa_circ_223097,RMVar_hsa_circ_31448,RMVar_hsa_circ_276935,RMVar_hsa_circ_293717,RMVar_hsa_circ_223098 2802 RMVar_ID_2802 Human_SNP_ID_166112795 A-to-I Human chr3 - 183087832 183087832 183087832 GGAGTCTCGCCCTGTTGCCCAGGCTGGAGTTCAGTGGCGCAATCTCGGCTCACTACAAGCTCCGC GGAGTCTCGCCCTGTTGCCCAGGCTGGAGTTCGGTGGCGCAATCTCGGCTCACTACAAGCTCCGC T C MCCC1 Ensembl:ENSG00000078070 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1428328176 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_223092,RMVar_hsa_circ_365888,RMVar_hsa_circ_223096,RMVar_hsa_circ_293363,RMVar_hsa_circ_333240,RMVar_hsa_circ_223095,RMVar_hsa_circ_265759,RMVar_hsa_circ_223097,RMVar_hsa_circ_31448,RMVar_hsa_circ_276935,RMVar_hsa_circ_293717,RMVar_hsa_circ_223098 2803 RMVar_ID_2803 Human_SNP_ID_166123563 A-to-I Human chr3 - 183127331 183127331 183127331 CAGGAGTTCAAGACCAGCCTGAGCAACATAGTAAGGACCCCATCTCTTCAAAAAAGTTAAAAAGT CAGGAGTTCAAGACCAGCCTGAGCAACATAGTGAGGACCCCATCTCTTCAAAAAAGTTAAAAAGT T C LAMP3 Ensembl:ENSG00000078081 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1246773438 Functional Loss SNV dbSNP153 33..33 33 - - - 2804 RMVar_ID_2804 Human_SNP_ID_166193759 A-to-I Human chr3 - 183420345 183420345 183420345 CACCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCACCTGGCCAGGTTGT CACCTGCCTTGGCCTCCCAAAGTGCTGGGATTGCAGGCATGAGCCACCGCACCTGGCCAGGTTGT T C MCF2L2 Ensembl:ENSG00000053524 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1039630696 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85312,RMVar_hsa_circ_223133 2805 RMVar_ID_2805 Human_SNP_ID_166193798 A-to-I Human chr3 - 183420516 183420516 183420516 CAGCACACTGCAACCTCCCACTCCTGGGGTTCAAGTGATTCTTCTGCCTCAGCCTCCCAATTAGC CAGCACACTGCAACCTCCCACTCCTGGGGTTCGAGTGATTCTTCTGCCTCAGCCTCCCAATTAGC T C MCF2L2 Ensembl:ENSG00000053524 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1327146747 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85312,RMVar_hsa_circ_223133 2806 RMVar_ID_2806 Human_SNP_ID_166211329 A-to-I Human chr3 - 183490656 183490656 183490656 GGATTACAGGCACCTGCCACCGCGCCTGGCTAATTTTTGTAGTTTTAGTAGAGACGGGGTTTCAC GGATTACAGGCACCTGCCACCGCGCCTGGCTACTTTTTGTAGTTTTAGTAGAGACGGGGTTTCAC T G KLHL6 Ensembl:ENSG00000172578 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1341446580 Functional Loss SNV dbSNP153 33..33 33 - - - 2807 RMVar_ID_2807 Human_SNP_ID_166211352 A-to-I Human chr3 - 183490722 183490722 183490722 CGGCTCACTGCAACCTCTGTCACCCTGGTTCAAGTGATTTTCCTGCCTCAGCCTCCTGAGTAGCT CGGCTCACTGCAACCTCTGTCACCCTGGTTCACGTGATTTTCCTGCCTCAGCCTCCTGAGTAGCT T G KLHL6 Ensembl:ENSG00000172578 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs542642350 Functional Loss SNV dbSNP153 33..33 33 - - - 2808 RMVar_ID_2808 Human_SNP_ID_166211522 A-to-I Human chr3 - 183491274 183491274 183491274 ACCGCCCCGTCTCTACTAAAAATACAAAAATTAGCCGCGTGCAGTGGCAGGCGCCTGTAATTCCA ACCGCCCCGTCTCTACTAAAAATACAAAAATTGGCCGCGTGCAGTGGCAGGCGCCTGTAATTCCA T C KLHL6 Ensembl:ENSG00000172578 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1019226159 Functional Loss SNV dbSNP153 33..33 33 - - - 2809 RMVar_ID_2809 Human_SNP_ID_166211523 A-to-I Human chr3 - 183491277 183491276 183491277 GAGACCGCCCCGTCTCTACTAAAAATACAAAAATTAGCCGCGTGCAGTGGCAGGCGCCTGTAATT GAGACCGCCCCGTCTCTACTAAAAATACAAAA_TTAGCCGCGTGCAGTGGCAGGCGCCTGTAATT AT A KLHL6 Ensembl:ENSG00000172578 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1485696491 Functional Loss DEL dbSNP153 33..33 33 - - - 2810 RMVar_ID_2810 Human_SNP_ID_166211524 A-to-I Human chr3 - 183491277 183491277 183491277 GAGACCGCCCCGTCTCTACTAAAAATACAAAAATTAGCCGCGTGCAGTGGCAGGCGCCTGTAATT GAGACCGCCCCGTCTCTACTAAAAATACAAAAGTTAGCCGCGTGCAGTGGCAGGCGCCTGTAATT T C KLHL6 Ensembl:ENSG00000172578 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs965675935 Functional Loss SNV dbSNP153 33..33 33 - - - 2811 RMVar_ID_2811 Human_SNP_ID_166248813 A-to-I Human chr3 + 183637788 183637788 183637788 TCAATCGATTCTCCTGCCTTAGTTTCCCGAGTAGCTGGGATGACAGGCGCCCGCCACCACGCCCG TCAATCGATTCTCCTGCCTTAGTTTCCCGAGTGGCTGGGATGACAGGCGCCCGCCACCACGCCCG A G KLHL24 Ensembl:ENSG00000114796 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1014142899 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94794,RMVar_hsa_circ_223134 2812 RMVar_ID_2812 Human_SNP_ID_166248827 A-to-I Human chr3 + 183637842 183637842 183637842 CACCACGCCCGGCTAGTTTTTGTATGTTTAGTAGGGACGGGGTTTCACCATGTTGGCCAGGCTAG CACCACGCCCGGCTAGTTTTTGTATGTTTAGTGGGGACGGGGTTTCACCATGTTGGCCAGGCTAG A G KLHL24 Ensembl:ENSG00000114796 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167902795 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94794,RMVar_hsa_circ_223134 2813 RMVar_ID_2813 Human_SNP_ID_166249752 A-to-I Human chr3 + 183640811 183640811 183640811 TTTAGTAGAAACGGGGTTTCACTATGTTGGCCAGGCTGGTCTCGAACCCTTGACCTCGTGATCCG TTTAGTAGAAACGGGGTTTCACTATGTTGGCCCGGCTGGTCTCGAACCCTTGACCTCGTGATCCG A C KLHL24 Ensembl:ENSG00000114796 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1472047357 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94794,RMVar_hsa_circ_223134 2814 RMVar_ID_2814 Human_SNP_ID_166253114 A-to-I Human chr3 + 183655371 183655369 183655372 GCTGTAGGCCAGGTGTGGTAGCTCACACCTGTAATCAAGCACTTTGGGAGGCCAAGGCATGGGGG GCTGTAGGCCAGGTGTGGTAGCTCACACCTG___TCAAGCACTTTGGGAGGCCAAGGCATGGGGG GTAA G KLHL24 Ensembl:ENSG00000114796 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1401326626 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_75193,RMVar_hsa_circ_223135,RMVar_hsa_circ_277568,RMVar_hsa_circ_331189,RMVar_hsa_circ_273653,RMVar_hsa_circ_126888,RMVar_hsa_circ_223145,RMVar_hsa_circ_223137,RMVar_hsa_circ_223139,RMVar_hsa_circ_223138,RMVar_hsa_circ_96237,RMVar_hsa_circ_223136,RMVar_hsa_circ_317448,RMVar_hsa_circ_288495,RMVar_hsa_circ_270289,RMVar_hsa_circ_223147,RMVar_hsa_circ_79055,RMVar_hsa_circ_223146,RMVar_hsa_circ_223143,RMVar_hsa_circ_223144,RMVar_hsa_circ_223142 2815 RMVar_ID_2815 Human_SNP_ID_166253215 A-to-I Human chr3 + 183655801 183655801 183655801 AAAAATTAGCAGACATGGTGGAGCGTGCCTGTAGTCCCATCTACTCGGGAGGCTGAGGAGGCTGA AAAAATTAGCAGACATGGTGGAGCGTGCCTGTGGTCCCATCTACTCGGGAGGCTGAGGAGGCTGA A G KLHL24 Ensembl:ENSG00000114796 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1354451412 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75193,RMVar_hsa_circ_223135,RMVar_hsa_circ_277568,RMVar_hsa_circ_331189,RMVar_hsa_circ_273653,RMVar_hsa_circ_126888,RMVar_hsa_circ_223145,RMVar_hsa_circ_223137,RMVar_hsa_circ_223139,RMVar_hsa_circ_223138,RMVar_hsa_circ_96237,RMVar_hsa_circ_223136,RMVar_hsa_circ_317448,RMVar_hsa_circ_288495,RMVar_hsa_circ_270289,RMVar_hsa_circ_223147,RMVar_hsa_circ_79055,RMVar_hsa_circ_223146,RMVar_hsa_circ_223143,RMVar_hsa_circ_223144,RMVar_hsa_circ_223142 2816 RMVar_ID_2816 Human_SNP_ID_166258525 A-to-I Human chr3 + 183677933 183677933 183677933 CCTGCCTCAGCCTCCCGAGTAGTAGGGATTACAAGCACCCCCCACCACGTCCAGCTAATTTTTTG CCTGCCTCAGCCTCCCGAGTAGTAGGGATTACGAGCACCCCCCACCACGTCCAGCTAATTTTTTG A G KLHL24 Ensembl:ENSG00000114796 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1016241285 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126888,RMVar_hsa_circ_223136,RMVar_hsa_circ_79055,RMVar_hsa_circ_223143,RMVar_hsa_circ_223142 2817 RMVar_ID_2817 Human_SNP_ID_166264545 A-to-I Human chr3 + 183701151 183701147 183701152 TCGCCCAGGCTGGAGTGCAGTGGCGCAATCTCAGCTCTCTGCAAGCTCTGCCTCCCGGGTTCACG TCGCCCAGGCTGGAGTGCAGTGGCGCAAT_____CTCTCTGCAAGCTCTGCCTCCCGGGTTCACG TCTCAG T YEATS2 Ensembl:ENSG00000163872 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1489307006 Functional Loss DEL dbSNP153 30..34 33 - - - RMVar_hsa_circ_95682,RMVar_hsa_circ_223153,RMVar_hsa_circ_121486,RMVar_hsa_circ_223154,RMVar_hsa_circ_223155 2818 RMVar_ID_2818 Human_SNP_ID_166272430 A-to-I Human chr3 + 183729720 183729720 183729720 TGAGACGGAGTTTCACTCTTGTCACACAGGCTAGAGTGCAGTGGTGTGCTGTTGGCTCACTGCAA TGAGACGGAGTTTCACTCTTGTCACACAGGCTGGAGTGCAGTGGTGTGCTGTTGGCTCACTGCAA A G YEATS2 Ensembl:ENSG00000163872 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1014887817 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_836292 RMVar_hsa_circ_95682,RMVar_hsa_circ_121486,RMVar_hsa_circ_223154,RMVar_hsa_circ_223155,RMVar_hsa_circ_268404,RMVar_hsa_circ_315976,RMVar_hsa_circ_332520,RMVar_hsa_circ_346893,RMVar_hsa_circ_315017,RMVar_hsa_circ_292065,RMVar_hsa_circ_9195,RMVar_hsa_circ_44478,RMVar_hsa_circ_6489,RMVar_hsa_circ_74353,RMVar_hsa_circ_223163,RMVar_hsa_circ_223164,RMVar_hsa_circ_310204,RMVar_hsa_circ_357245,RMVar_hsa_circ_374779,RMVar_hsa_circ_333746,RMVar_hsa_circ_307692,RMVar_hsa_circ_293768,RMVar_hsa_circ_276493,RMVar_hsa_circ_96889,RMVar_hsa_circ_223167,RMVar_hsa_circ_62303,RMVar_hsa_circ_67680,RMVar_hsa_circ_5524,RMVar_hsa_circ_223169,RMVar_hsa_circ_223168,RMVar_hsa_circ_223165,RMVar_hsa_circ_223166,RMVar_hsa_circ_18836,RMVar_hsa_circ_77641,RMVar_hsa_circ_114457,RMVar_hsa_circ_223175,RMVar_hsa_circ_34606,RMVar_hsa_circ_52785,RMVar_hsa_circ_334114,RMVar_hsa_circ_223176,RMVar_hsa_circ_334163,RMVar_hsa_circ_15827,RMVar_hsa_circ_29035,RMVar_hsa_circ_223178,RMVar_hsa_circ_223179,RMVar_hsa_circ_223180,RMVar_hsa_circ_293674,RMVar_hsa_circ_364451,RMVar_hsa_circ_223181 2819 RMVar_ID_2819 Human_SNP_ID_166273179 A-to-I Human chr3 + 183732195 183732179 183732195 AGGGTCGGCTGGGCACCGTGGCTCAAGCCTGTAATCCCAGCACTTTGGGAGACTGAGGCAGGTGG AGGGTCGGCTGGGCACC________________ATCCCAGCACTTTGGGAGACTGAGGCAGGTGG CGTGGCTCAAGCCTGTA C YEATS2 Ensembl:ENSG00000163872 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1265663894 Functional Loss DEL dbSNP153 18..33 33 - - - RMVar_hsa_circ_95682,RMVar_hsa_circ_121486,RMVar_hsa_circ_223154,RMVar_hsa_circ_223155,RMVar_hsa_circ_268404,RMVar_hsa_circ_315976,RMVar_hsa_circ_332520,RMVar_hsa_circ_346893,RMVar_hsa_circ_315017,RMVar_hsa_circ_292065,RMVar_hsa_circ_9195,RMVar_hsa_circ_44478,RMVar_hsa_circ_6489,RMVar_hsa_circ_74353,RMVar_hsa_circ_223163,RMVar_hsa_circ_223164,RMVar_hsa_circ_310204,RMVar_hsa_circ_357245,RMVar_hsa_circ_374779,RMVar_hsa_circ_333746,RMVar_hsa_circ_307692,RMVar_hsa_circ_293768,RMVar_hsa_circ_276493,RMVar_hsa_circ_96889,RMVar_hsa_circ_223167,RMVar_hsa_circ_62303,RMVar_hsa_circ_67680,RMVar_hsa_circ_5524,RMVar_hsa_circ_223169,RMVar_hsa_circ_223168,RMVar_hsa_circ_223165,RMVar_hsa_circ_223166,RMVar_hsa_circ_18836,RMVar_hsa_circ_77641,RMVar_hsa_circ_114457,RMVar_hsa_circ_223175,RMVar_hsa_circ_34606,RMVar_hsa_circ_52785,RMVar_hsa_circ_334114,RMVar_hsa_circ_223176,RMVar_hsa_circ_334163,RMVar_hsa_circ_15827,RMVar_hsa_circ_29035,RMVar_hsa_circ_223178,RMVar_hsa_circ_223179,RMVar_hsa_circ_223180,RMVar_hsa_circ_293674,RMVar_hsa_circ_364451,RMVar_hsa_circ_223181 2820 RMVar_ID_2820 Human_SNP_ID_166273210 A-to-I Human chr3 + 183732265 183732265 183732265 GAGATCAGGCGTTTGAGACCAGCCTTGCCAACATGGTGAAACCTTGTCTCTACTAAAAATACAAA GAGATCAGGCGTTTGAGACCAGCCTTGCCAACCTGGTGAAACCTTGTCTCTACTAAAAATACAAA A C YEATS2 Ensembl:ENSG00000163872 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs570242049 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95682,RMVar_hsa_circ_121486,RMVar_hsa_circ_223154,RMVar_hsa_circ_223155,RMVar_hsa_circ_268404,RMVar_hsa_circ_315976,RMVar_hsa_circ_332520,RMVar_hsa_circ_346893,RMVar_hsa_circ_315017,RMVar_hsa_circ_292065,RMVar_hsa_circ_9195,RMVar_hsa_circ_44478,RMVar_hsa_circ_6489,RMVar_hsa_circ_74353,RMVar_hsa_circ_223163,RMVar_hsa_circ_223164,RMVar_hsa_circ_310204,RMVar_hsa_circ_357245,RMVar_hsa_circ_374779,RMVar_hsa_circ_333746,RMVar_hsa_circ_307692,RMVar_hsa_circ_293768,RMVar_hsa_circ_276493,RMVar_hsa_circ_96889,RMVar_hsa_circ_223167,RMVar_hsa_circ_62303,RMVar_hsa_circ_67680,RMVar_hsa_circ_5524,RMVar_hsa_circ_223169,RMVar_hsa_circ_223168,RMVar_hsa_circ_223165,RMVar_hsa_circ_223166,RMVar_hsa_circ_18836,RMVar_hsa_circ_77641,RMVar_hsa_circ_114457,RMVar_hsa_circ_223175,RMVar_hsa_circ_34606,RMVar_hsa_circ_52785,RMVar_hsa_circ_334114,RMVar_hsa_circ_223176,RMVar_hsa_circ_334163,RMVar_hsa_circ_15827,RMVar_hsa_circ_29035,RMVar_hsa_circ_223178,RMVar_hsa_circ_223179,RMVar_hsa_circ_223180,RMVar_hsa_circ_293674,RMVar_hsa_circ_364451,RMVar_hsa_circ_223181 2821 RMVar_ID_2821 Human_SNP_ID_166273211 A-to-I Human chr3 + 183732265 183732265 183732265 GAGATCAGGCGTTTGAGACCAGCCTTGCCAACATGGTGAAACCTTGTCTCTACTAAAAATACAAA GAGATCAGGCGTTTGAGACCAGCCTTGCCAACGTGGTGAAACCTTGTCTCTACTAAAAATACAAA A G YEATS2 Ensembl:ENSG00000163872 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs570242049 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95682,RMVar_hsa_circ_121486,RMVar_hsa_circ_223154,RMVar_hsa_circ_223155,RMVar_hsa_circ_268404,RMVar_hsa_circ_315976,RMVar_hsa_circ_332520,RMVar_hsa_circ_346893,RMVar_hsa_circ_315017,RMVar_hsa_circ_292065,RMVar_hsa_circ_9195,RMVar_hsa_circ_44478,RMVar_hsa_circ_6489,RMVar_hsa_circ_74353,RMVar_hsa_circ_223163,RMVar_hsa_circ_223164,RMVar_hsa_circ_310204,RMVar_hsa_circ_357245,RMVar_hsa_circ_374779,RMVar_hsa_circ_333746,RMVar_hsa_circ_307692,RMVar_hsa_circ_293768,RMVar_hsa_circ_276493,RMVar_hsa_circ_96889,RMVar_hsa_circ_223167,RMVar_hsa_circ_62303,RMVar_hsa_circ_67680,RMVar_hsa_circ_5524,RMVar_hsa_circ_223169,RMVar_hsa_circ_223168,RMVar_hsa_circ_223165,RMVar_hsa_circ_223166,RMVar_hsa_circ_18836,RMVar_hsa_circ_77641,RMVar_hsa_circ_114457,RMVar_hsa_circ_223175,RMVar_hsa_circ_34606,RMVar_hsa_circ_52785,RMVar_hsa_circ_334114,RMVar_hsa_circ_223176,RMVar_hsa_circ_334163,RMVar_hsa_circ_15827,RMVar_hsa_circ_29035,RMVar_hsa_circ_223178,RMVar_hsa_circ_223179,RMVar_hsa_circ_223180,RMVar_hsa_circ_293674,RMVar_hsa_circ_364451,RMVar_hsa_circ_223181 2822 RMVar_ID_2822 Human_SNP_ID_166275423 A-to-I Human chr3 + 183741136 183741136 183741136 AATTTTTGTATTTTTAGTAGAAATAGGGTTTCACCGTGTTGTCCTGGCTGGTCTCAAACTCCTGA AATTTTTGTATTTTTAGTAGAAATAGGGTTTCTCCGTGTTGTCCTGGCTGGTCTCAAACTCCTGA A T YEATS2 Ensembl:ENSG00000163872 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1198333928 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22726180 RMVar_hsa_circ_3315,RMVar_hsa_circ_95682,RMVar_hsa_circ_121486,RMVar_hsa_circ_223154,RMVar_hsa_circ_223155,RMVar_hsa_circ_268404,RMVar_hsa_circ_315976,RMVar_hsa_circ_346893,RMVar_hsa_circ_315017,RMVar_hsa_circ_292065,RMVar_hsa_circ_9195,RMVar_hsa_circ_44478,RMVar_hsa_circ_6489,RMVar_hsa_circ_74353,RMVar_hsa_circ_223163,RMVar_hsa_circ_223164,RMVar_hsa_circ_310204,RMVar_hsa_circ_357245,RMVar_hsa_circ_374779,RMVar_hsa_circ_333746,RMVar_hsa_circ_307692,RMVar_hsa_circ_293768,RMVar_hsa_circ_276493,RMVar_hsa_circ_96889,RMVar_hsa_circ_223167,RMVar_hsa_circ_62303,RMVar_hsa_circ_67680,RMVar_hsa_circ_5524,RMVar_hsa_circ_223169,RMVar_hsa_circ_223168,RMVar_hsa_circ_223165,RMVar_hsa_circ_223166,RMVar_hsa_circ_18836,RMVar_hsa_circ_77641,RMVar_hsa_circ_114457,RMVar_hsa_circ_223175,RMVar_hsa_circ_52785,RMVar_hsa_circ_334114,RMVar_hsa_circ_223176,RMVar_hsa_circ_334163,RMVar_hsa_circ_15827,RMVar_hsa_circ_29035,RMVar_hsa_circ_223178,RMVar_hsa_circ_223179,RMVar_hsa_circ_76043,RMVar_hsa_circ_223180,RMVar_hsa_circ_293674,RMVar_hsa_circ_364451,RMVar_hsa_circ_223181,RMVar_hsa_circ_281628,RMVar_hsa_circ_302589,RMVar_hsa_circ_311778,RMVar_hsa_circ_295617,RMVar_hsa_circ_281082,RMVar_hsa_circ_44158,RMVar_hsa_circ_51505,RMVar_hsa_circ_38709,RMVar_hsa_circ_223184,RMVar_hsa_circ_223186,RMVar_hsa_circ_223188,RMVar_hsa_circ_223189,RMVar_hsa_circ_223187,RMVar_hsa_circ_223185,RMVar_hsa_circ_223183 2823 RMVar_ID_2823 Human_SNP_ID_166282677 A-to-I Human chr3 + 183767542 183767542 183767542 AGCTGGGATTACAGGCACCCACCACCATGCCTAGCTAATTTTTTTGTATTTTTAGTAGAGACAGG AGCTGGGATTACAGGCACCCACCACCATGCCTGGCTAATTTTTTTGTATTTTTAGTAGAGACAGG A G YEATS2 Ensembl:ENSG00000163872 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs369231114 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3315,RMVar_hsa_circ_268404,RMVar_hsa_circ_9195,RMVar_hsa_circ_74353,RMVar_hsa_circ_357245,RMVar_hsa_circ_374779,RMVar_hsa_circ_307692,RMVar_hsa_circ_96889,RMVar_hsa_circ_62303,RMVar_hsa_circ_223165,RMVar_hsa_circ_223166,RMVar_hsa_circ_18836,RMVar_hsa_circ_77641,RMVar_hsa_circ_114457,RMVar_hsa_circ_223175,RMVar_hsa_circ_223176,RMVar_hsa_circ_76043,RMVar_hsa_circ_295617,RMVar_hsa_circ_38709,RMVar_hsa_circ_99840,RMVar_hsa_circ_48728,RMVar_hsa_circ_120074,RMVar_hsa_circ_223184,RMVar_hsa_circ_223183,RMVar_hsa_circ_303412,RMVar_hsa_circ_283070,RMVar_hsa_circ_103962,RMVar_hsa_circ_116923,RMVar_hsa_circ_86944,RMVar_hsa_circ_26433,RMVar_hsa_circ_223191,RMVar_hsa_circ_223195,RMVar_hsa_circ_18261,RMVar_hsa_circ_223193,RMVar_hsa_circ_223194,RMVar_hsa_circ_223192,RMVar_hsa_circ_52360,RMVar_hsa_circ_223190,RMVar_hsa_circ_352913,RMVar_hsa_circ_223200,RMVar_hsa_circ_49691,RMVar_hsa_circ_71679,RMVar_hsa_circ_122361,RMVar_hsa_circ_377071,RMVar_hsa_circ_105810,RMVar_hsa_circ_117039,RMVar_hsa_circ_223202,RMVar_hsa_circ_223204,RMVar_hsa_circ_223203,RMVar_hsa_circ_127150,RMVar_hsa_circ_348578,RMVar_hsa_circ_372828,RMVar_hsa_circ_223201,RMVar_hsa_circ_223209,RMVar_hsa_circ_223211,RMVar_hsa_circ_111494,RMVar_hsa_circ_223212,RMVar_hsa_circ_223210,RMVar_hsa_circ_28287,RMVar_hsa_circ_344788,RMVar_hsa_circ_223208,RMVar_hsa_circ_223217,RMVar_hsa_circ_64448,RMVar_hsa_circ_350603,RMVar_hsa_circ_363489,RMVar_hsa_circ_47480 2824 RMVar_ID_2824 Human_SNP_ID_166282682 A-to-I Human chr3 + 183767557 183767557 183767557 CACCCACCACCATGCCTAGCTAATTTTTTTGTATTTTTAGTAGAGACAGGGTTTCACTATGTTGG CACCCACCACCATGCCTAGCTAATTTTTTTGTGTTTTTAGTAGAGACAGGGTTTCACTATGTTGG A G YEATS2 Ensembl:ENSG00000163872 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs557085762 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3315,RMVar_hsa_circ_268404,RMVar_hsa_circ_9195,RMVar_hsa_circ_74353,RMVar_hsa_circ_357245,RMVar_hsa_circ_374779,RMVar_hsa_circ_307692,RMVar_hsa_circ_96889,RMVar_hsa_circ_62303,RMVar_hsa_circ_223165,RMVar_hsa_circ_223166,RMVar_hsa_circ_18836,RMVar_hsa_circ_77641,RMVar_hsa_circ_114457,RMVar_hsa_circ_223175,RMVar_hsa_circ_223176,RMVar_hsa_circ_76043,RMVar_hsa_circ_295617,RMVar_hsa_circ_38709,RMVar_hsa_circ_99840,RMVar_hsa_circ_48728,RMVar_hsa_circ_120074,RMVar_hsa_circ_223184,RMVar_hsa_circ_223183,RMVar_hsa_circ_303412,RMVar_hsa_circ_283070,RMVar_hsa_circ_103962,RMVar_hsa_circ_116923,RMVar_hsa_circ_86944,RMVar_hsa_circ_26433,RMVar_hsa_circ_223191,RMVar_hsa_circ_223195,RMVar_hsa_circ_18261,RMVar_hsa_circ_223193,RMVar_hsa_circ_223194,RMVar_hsa_circ_223192,RMVar_hsa_circ_52360,RMVar_hsa_circ_223190,RMVar_hsa_circ_352913,RMVar_hsa_circ_223200,RMVar_hsa_circ_49691,RMVar_hsa_circ_71679,RMVar_hsa_circ_122361,RMVar_hsa_circ_377071,RMVar_hsa_circ_105810,RMVar_hsa_circ_117039,RMVar_hsa_circ_223202,RMVar_hsa_circ_223204,RMVar_hsa_circ_223203,RMVar_hsa_circ_127150,RMVar_hsa_circ_348578,RMVar_hsa_circ_372828,RMVar_hsa_circ_223201,RMVar_hsa_circ_223209,RMVar_hsa_circ_223211,RMVar_hsa_circ_111494,RMVar_hsa_circ_223212,RMVar_hsa_circ_223210,RMVar_hsa_circ_28287,RMVar_hsa_circ_344788,RMVar_hsa_circ_223208,RMVar_hsa_circ_223217,RMVar_hsa_circ_64448,RMVar_hsa_circ_350603,RMVar_hsa_circ_363489,RMVar_hsa_circ_47480 2825 RMVar_ID_2825 Human_SNP_ID_166282683 A-to-I Human chr3 + 183767557 183767557 183767557 CACCCACCACCATGCCTAGCTAATTTTTTTGTATTTTTAGTAGAGACAGGGTTTCACTATGTTGG CACCCACCACCATGCCTAGCTAATTTTTTTGTTTTTTTAGTAGAGACAGGGTTTCACTATGTTGG A T YEATS2 Ensembl:ENSG00000163872 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs557085762 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3315,RMVar_hsa_circ_268404,RMVar_hsa_circ_9195,RMVar_hsa_circ_74353,RMVar_hsa_circ_357245,RMVar_hsa_circ_374779,RMVar_hsa_circ_307692,RMVar_hsa_circ_96889,RMVar_hsa_circ_62303,RMVar_hsa_circ_223165,RMVar_hsa_circ_223166,RMVar_hsa_circ_18836,RMVar_hsa_circ_77641,RMVar_hsa_circ_114457,RMVar_hsa_circ_223175,RMVar_hsa_circ_223176,RMVar_hsa_circ_76043,RMVar_hsa_circ_295617,RMVar_hsa_circ_38709,RMVar_hsa_circ_99840,RMVar_hsa_circ_48728,RMVar_hsa_circ_120074,RMVar_hsa_circ_223184,RMVar_hsa_circ_223183,RMVar_hsa_circ_303412,RMVar_hsa_circ_283070,RMVar_hsa_circ_103962,RMVar_hsa_circ_116923,RMVar_hsa_circ_86944,RMVar_hsa_circ_26433,RMVar_hsa_circ_223191,RMVar_hsa_circ_223195,RMVar_hsa_circ_18261,RMVar_hsa_circ_223193,RMVar_hsa_circ_223194,RMVar_hsa_circ_223192,RMVar_hsa_circ_52360,RMVar_hsa_circ_223190,RMVar_hsa_circ_352913,RMVar_hsa_circ_223200,RMVar_hsa_circ_49691,RMVar_hsa_circ_71679,RMVar_hsa_circ_122361,RMVar_hsa_circ_377071,RMVar_hsa_circ_105810,RMVar_hsa_circ_117039,RMVar_hsa_circ_223202,RMVar_hsa_circ_223204,RMVar_hsa_circ_223203,RMVar_hsa_circ_127150,RMVar_hsa_circ_348578,RMVar_hsa_circ_372828,RMVar_hsa_circ_223201,RMVar_hsa_circ_223209,RMVar_hsa_circ_223211,RMVar_hsa_circ_111494,RMVar_hsa_circ_223212,RMVar_hsa_circ_223210,RMVar_hsa_circ_28287,RMVar_hsa_circ_344788,RMVar_hsa_circ_223208,RMVar_hsa_circ_223217,RMVar_hsa_circ_64448,RMVar_hsa_circ_350603,RMVar_hsa_circ_363489,RMVar_hsa_circ_47480 2826 RMVar_ID_2826 Human_SNP_ID_166283258 A-to-I Human chr3 + 183769717 183769716 183769718 CTGTTTTCATTTTATTTATTTATTGTTTAGACAGAGTCTTGCTCTGTCGCCAGGCTAGAGTGCAG CTGTTTTCATTTTATTTATTTATTGTTTAGAC__AGTCTTGCTCTGTCGCCAGGCTAGAGTGCAG CAG C YEATS2 Ensembl:ENSG00000163872 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs545847957 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_3315,RMVar_hsa_circ_268404,RMVar_hsa_circ_9195,RMVar_hsa_circ_74353,RMVar_hsa_circ_357245,RMVar_hsa_circ_374779,RMVar_hsa_circ_307692,RMVar_hsa_circ_96889,RMVar_hsa_circ_62303,RMVar_hsa_circ_223165,RMVar_hsa_circ_223166,RMVar_hsa_circ_18836,RMVar_hsa_circ_77641,RMVar_hsa_circ_114457,RMVar_hsa_circ_223175,RMVar_hsa_circ_223176,RMVar_hsa_circ_76043,RMVar_hsa_circ_295617,RMVar_hsa_circ_38709,RMVar_hsa_circ_99840,RMVar_hsa_circ_48728,RMVar_hsa_circ_120074,RMVar_hsa_circ_223184,RMVar_hsa_circ_223183,RMVar_hsa_circ_303412,RMVar_hsa_circ_283070,RMVar_hsa_circ_103962,RMVar_hsa_circ_116923,RMVar_hsa_circ_86944,RMVar_hsa_circ_26433,RMVar_hsa_circ_223191,RMVar_hsa_circ_223195,RMVar_hsa_circ_18261,RMVar_hsa_circ_223193,RMVar_hsa_circ_223194,RMVar_hsa_circ_223192,RMVar_hsa_circ_52360,RMVar_hsa_circ_223190,RMVar_hsa_circ_352913,RMVar_hsa_circ_223200,RMVar_hsa_circ_49691,RMVar_hsa_circ_71679,RMVar_hsa_circ_122361,RMVar_hsa_circ_377071,RMVar_hsa_circ_105810,RMVar_hsa_circ_117039,RMVar_hsa_circ_223202,RMVar_hsa_circ_223204,RMVar_hsa_circ_223203,RMVar_hsa_circ_127150,RMVar_hsa_circ_348578,RMVar_hsa_circ_372828,RMVar_hsa_circ_223201,RMVar_hsa_circ_223209,RMVar_hsa_circ_223211,RMVar_hsa_circ_111494,RMVar_hsa_circ_223212,RMVar_hsa_circ_223210,RMVar_hsa_circ_28287,RMVar_hsa_circ_344788,RMVar_hsa_circ_223208,RMVar_hsa_circ_223217,RMVar_hsa_circ_64448,RMVar_hsa_circ_350603,RMVar_hsa_circ_363489,RMVar_hsa_circ_47480 2827 RMVar_ID_2827 Human_SNP_ID_166285827 A-to-I Human chr3 + 183778577 183778577 183778577 GGGGTTTCTCCATGTTGGTCAGGCTGGTCTCCAGCTCGTGACCTCAGGTGATCTGCCCGCCTCGG GGGGTTTCTCCATGTTGGTCAGGCTGGTCTCCCGCTCGTGACCTCAGGTGATCTGCCCGCCTCGG A C YEATS2 Ensembl:ENSG00000163872 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1321023170 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9195,RMVar_hsa_circ_74353,RMVar_hsa_circ_357245,RMVar_hsa_circ_96889,RMVar_hsa_circ_62303,RMVar_hsa_circ_223165,RMVar_hsa_circ_18836,RMVar_hsa_circ_114457,RMVar_hsa_circ_223176,RMVar_hsa_circ_76043,RMVar_hsa_circ_295617,RMVar_hsa_circ_38709,RMVar_hsa_circ_8462,RMVar_hsa_circ_99840,RMVar_hsa_circ_120074,RMVar_hsa_circ_223184,RMVar_hsa_circ_223183,RMVar_hsa_circ_283070,RMVar_hsa_circ_103962,RMVar_hsa_circ_116923,RMVar_hsa_circ_86944,RMVar_hsa_circ_223191,RMVar_hsa_circ_18261,RMVar_hsa_circ_223193,RMVar_hsa_circ_223194,RMVar_hsa_circ_223192,RMVar_hsa_circ_223190,RMVar_hsa_circ_49691,RMVar_hsa_circ_122361,RMVar_hsa_circ_377071,RMVar_hsa_circ_117039,RMVar_hsa_circ_223202,RMVar_hsa_circ_223203,RMVar_hsa_circ_127150,RMVar_hsa_circ_223201,RMVar_hsa_circ_223209,RMVar_hsa_circ_111494,RMVar_hsa_circ_223210,RMVar_hsa_circ_28287,RMVar_hsa_circ_223208,RMVar_hsa_circ_64448,RMVar_hsa_circ_47480,RMVar_hsa_circ_5404,RMVar_hsa_circ_345741,RMVar_hsa_circ_375753,RMVar_hsa_circ_337753,RMVar_hsa_circ_127788,RMVar_hsa_circ_269810,RMVar_hsa_circ_44426,RMVar_hsa_circ_223221,RMVar_hsa_circ_223222,RMVar_hsa_circ_223223,RMVar_hsa_circ_223220,RMVar_hsa_circ_86919,RMVar_hsa_circ_117939,RMVar_hsa_circ_120439,RMVar_hsa_circ_371536,RMVar_hsa_circ_110941,RMVar_hsa_circ_43308,RMVar_hsa_circ_82475,RMVar_hsa_circ_40511,RMVar_hsa_circ_223231,RMVar_hsa_circ_85757,RMVar_hsa_circ_223224,RMVar_hsa_circ_223226,RMVar_hsa_circ_223228,RMVar_hsa_circ_223229,RMVar_hsa_circ_223227,RMVar_hsa_circ_223225,RMVar_hsa_circ_275036,RMVar_hsa_circ_288537,RMVar_hsa_circ_278527,RMVar_hsa_circ_122357,RMVar_hsa_circ_90312,RMVar_hsa_circ_223233,RMVar_hsa_circ_223235,RMVar_hsa_circ_19716,RMVar_hsa_circ_223234,RMVar_hsa_circ_223232,RMVar_hsa_circ_84026,RMVar_hsa_circ_323828,RMVar_hsa_circ_223230,RMVar_hsa_circ_285735,RMVar_hsa_circ_223240,RMVar_hsa_circ_223241,RMVar_hsa_circ_223239 2828 RMVar_ID_2828 Human_SNP_ID_166288006 A-to-I Human chr3 + 183786954 183786954 183786954 TACCTAGTGATGGAATTGCTGGATTATAAGGTAACTTTTTTTGTTGTTTTTTGAGATGGAGTCTT TACCTAGTGATGGAATTGCTGGATTATAAGGTGACTTTTTTTGTTGTTTTTTGAGATGGAGTCTT A G YEATS2 Ensembl:ENSG00000163872 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs774901239 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9195,RMVar_hsa_circ_74353,RMVar_hsa_circ_96889,RMVar_hsa_circ_62303,RMVar_hsa_circ_223165,RMVar_hsa_circ_114457,RMVar_hsa_circ_223176,RMVar_hsa_circ_76043,RMVar_hsa_circ_38709,RMVar_hsa_circ_8462,RMVar_hsa_circ_99840,RMVar_hsa_circ_120074,RMVar_hsa_circ_223183,RMVar_hsa_circ_103962,RMVar_hsa_circ_116923,RMVar_hsa_circ_86944,RMVar_hsa_circ_223191,RMVar_hsa_circ_18261,RMVar_hsa_circ_223193,RMVar_hsa_circ_223192,RMVar_hsa_circ_223190,RMVar_hsa_circ_122361,RMVar_hsa_circ_377071,RMVar_hsa_circ_117039,RMVar_hsa_circ_223202,RMVar_hsa_circ_223203,RMVar_hsa_circ_127150,RMVar_hsa_circ_223201,RMVar_hsa_circ_223209,RMVar_hsa_circ_111494,RMVar_hsa_circ_223210,RMVar_hsa_circ_28287,RMVar_hsa_circ_223208,RMVar_hsa_circ_5404,RMVar_hsa_circ_345741,RMVar_hsa_circ_375753,RMVar_hsa_circ_127788,RMVar_hsa_circ_269810,RMVar_hsa_circ_44426,RMVar_hsa_circ_223221,RMVar_hsa_circ_223222,RMVar_hsa_circ_223223,RMVar_hsa_circ_86919,RMVar_hsa_circ_117939,RMVar_hsa_circ_120439,RMVar_hsa_circ_110941,RMVar_hsa_circ_43308,RMVar_hsa_circ_82475,RMVar_hsa_circ_40511,RMVar_hsa_circ_223231,RMVar_hsa_circ_85757,RMVar_hsa_circ_223224,RMVar_hsa_circ_223226,RMVar_hsa_circ_223228,RMVar_hsa_circ_223227,RMVar_hsa_circ_223225,RMVar_hsa_circ_275036,RMVar_hsa_circ_278527,RMVar_hsa_circ_122357,RMVar_hsa_circ_90312,RMVar_hsa_circ_223233,RMVar_hsa_circ_19716,RMVar_hsa_circ_223234,RMVar_hsa_circ_223232,RMVar_hsa_circ_27637,RMVar_hsa_circ_84026,RMVar_hsa_circ_223230,RMVar_hsa_circ_285735,RMVar_hsa_circ_223240,RMVar_hsa_circ_223241,RMVar_hsa_circ_295334,RMVar_hsa_circ_46402,RMVar_hsa_circ_223243 2829 RMVar_ID_2829 Human_SNP_ID_166289832 A-to-I Human chr3 + 183793631 183793631 183793631 TTCTTTCTTTCTTTTTTTTTTTTTTTTTTTTGAGATGGAATTTTGTTCTTGTCGCCCAGTCTGGA TTCTTTCTTTCTTTTTTTTTTTTTTTTTTTTGTGATGGAATTTTGTTCTTGTCGCCCAGTCTGGA A T YEATS2 Ensembl:ENSG00000163872 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1209456200 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14743034 RMVar_hsa_circ_9195,RMVar_hsa_circ_74353,RMVar_hsa_circ_62303,RMVar_hsa_circ_114457,RMVar_hsa_circ_223176,RMVar_hsa_circ_76043,RMVar_hsa_circ_38709,RMVar_hsa_circ_8462,RMVar_hsa_circ_99840,RMVar_hsa_circ_120074,RMVar_hsa_circ_223183,RMVar_hsa_circ_103962,RMVar_hsa_circ_116923,RMVar_hsa_circ_86944,RMVar_hsa_circ_223191,RMVar_hsa_circ_18261,RMVar_hsa_circ_223193,RMVar_hsa_circ_223192,RMVar_hsa_circ_223190,RMVar_hsa_circ_377071,RMVar_hsa_circ_117039,RMVar_hsa_circ_223202,RMVar_hsa_circ_127150,RMVar_hsa_circ_223201,RMVar_hsa_circ_223209,RMVar_hsa_circ_111494,RMVar_hsa_circ_223210,RMVar_hsa_circ_28287,RMVar_hsa_circ_223208,RMVar_hsa_circ_5404,RMVar_hsa_circ_375753,RMVar_hsa_circ_127788,RMVar_hsa_circ_269810,RMVar_hsa_circ_44426,RMVar_hsa_circ_223222,RMVar_hsa_circ_223223,RMVar_hsa_circ_86919,RMVar_hsa_circ_117939,RMVar_hsa_circ_120439,RMVar_hsa_circ_110941,RMVar_hsa_circ_82475,RMVar_hsa_circ_40511,RMVar_hsa_circ_223231,RMVar_hsa_circ_85757,RMVar_hsa_circ_223224,RMVar_hsa_circ_223226,RMVar_hsa_circ_223228,RMVar_hsa_circ_223227,RMVar_hsa_circ_223225,RMVar_hsa_circ_275036,RMVar_hsa_circ_122357,RMVar_hsa_circ_90312,RMVar_hsa_circ_223233,RMVar_hsa_circ_19716,RMVar_hsa_circ_223232,RMVar_hsa_circ_27637,RMVar_hsa_circ_84026,RMVar_hsa_circ_223230,RMVar_hsa_circ_223241,RMVar_hsa_circ_46402,RMVar_hsa_circ_223244,RMVar_hsa_circ_91678 2830 RMVar_ID_2830 Human_SNP_ID_166289866 A-to-I Human chr3 + 183793742 183793742 183793742 TCCAGCGATTCTCCTGCCTCAGCCTCTTGAGTAGCTGGGATTATAGGCGTGTGCCACCACGTCCC TCCAGCGATTCTCCTGCCTCAGCCTCTTGAGTGGCTGGGATTATAGGCGTGTGCCACCACGTCCC A G YEATS2 Ensembl:ENSG00000163872 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1210745987 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9195,RMVar_hsa_circ_74353,RMVar_hsa_circ_62303,RMVar_hsa_circ_114457,RMVar_hsa_circ_223176,RMVar_hsa_circ_76043,RMVar_hsa_circ_38709,RMVar_hsa_circ_8462,RMVar_hsa_circ_99840,RMVar_hsa_circ_120074,RMVar_hsa_circ_223183,RMVar_hsa_circ_103962,RMVar_hsa_circ_116923,RMVar_hsa_circ_86944,RMVar_hsa_circ_223191,RMVar_hsa_circ_18261,RMVar_hsa_circ_223193,RMVar_hsa_circ_223192,RMVar_hsa_circ_223190,RMVar_hsa_circ_377071,RMVar_hsa_circ_117039,RMVar_hsa_circ_223202,RMVar_hsa_circ_127150,RMVar_hsa_circ_223201,RMVar_hsa_circ_223209,RMVar_hsa_circ_111494,RMVar_hsa_circ_223210,RMVar_hsa_circ_28287,RMVar_hsa_circ_223208,RMVar_hsa_circ_5404,RMVar_hsa_circ_375753,RMVar_hsa_circ_127788,RMVar_hsa_circ_269810,RMVar_hsa_circ_44426,RMVar_hsa_circ_223222,RMVar_hsa_circ_223223,RMVar_hsa_circ_86919,RMVar_hsa_circ_117939,RMVar_hsa_circ_120439,RMVar_hsa_circ_110941,RMVar_hsa_circ_82475,RMVar_hsa_circ_40511,RMVar_hsa_circ_223231,RMVar_hsa_circ_85757,RMVar_hsa_circ_223224,RMVar_hsa_circ_223226,RMVar_hsa_circ_223228,RMVar_hsa_circ_223227,RMVar_hsa_circ_223225,RMVar_hsa_circ_275036,RMVar_hsa_circ_122357,RMVar_hsa_circ_90312,RMVar_hsa_circ_223233,RMVar_hsa_circ_19716,RMVar_hsa_circ_223232,RMVar_hsa_circ_27637,RMVar_hsa_circ_84026,RMVar_hsa_circ_223230,RMVar_hsa_circ_223241,RMVar_hsa_circ_46402,RMVar_hsa_circ_223244,RMVar_hsa_circ_91678 2831 RMVar_ID_2831 Human_SNP_ID_166290147 A-to-I Human chr3 + 183794999 183794999 183794999 TGAGACAAGCCTGGGCAATGTGACAAGACCCCATTTCTTAAAAAAAAAAAAAATTAGCTGGGCAT TGAGACAAGCCTGGGCAATGTGACAAGACCCCGTTTCTTAAAAAAAAAAAAAATTAGCTGGGCAT A G YEATS2 Ensembl:ENSG00000163872 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909821999 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9195,RMVar_hsa_circ_74353,RMVar_hsa_circ_62303,RMVar_hsa_circ_114457,RMVar_hsa_circ_223176,RMVar_hsa_circ_76043,RMVar_hsa_circ_38709,RMVar_hsa_circ_8462,RMVar_hsa_circ_99840,RMVar_hsa_circ_120074,RMVar_hsa_circ_223183,RMVar_hsa_circ_103962,RMVar_hsa_circ_116923,RMVar_hsa_circ_86944,RMVar_hsa_circ_223191,RMVar_hsa_circ_18261,RMVar_hsa_circ_223193,RMVar_hsa_circ_223192,RMVar_hsa_circ_223190,RMVar_hsa_circ_377071,RMVar_hsa_circ_117039,RMVar_hsa_circ_223202,RMVar_hsa_circ_127150,RMVar_hsa_circ_223201,RMVar_hsa_circ_223209,RMVar_hsa_circ_111494,RMVar_hsa_circ_223210,RMVar_hsa_circ_28287,RMVar_hsa_circ_223208,RMVar_hsa_circ_5404,RMVar_hsa_circ_375753,RMVar_hsa_circ_127788,RMVar_hsa_circ_269810,RMVar_hsa_circ_44426,RMVar_hsa_circ_223222,RMVar_hsa_circ_223223,RMVar_hsa_circ_86919,RMVar_hsa_circ_117939,RMVar_hsa_circ_120439,RMVar_hsa_circ_110941,RMVar_hsa_circ_82475,RMVar_hsa_circ_40511,RMVar_hsa_circ_223231,RMVar_hsa_circ_85757,RMVar_hsa_circ_223224,RMVar_hsa_circ_223226,RMVar_hsa_circ_223228,RMVar_hsa_circ_223227,RMVar_hsa_circ_223225,RMVar_hsa_circ_275036,RMVar_hsa_circ_122357,RMVar_hsa_circ_90312,RMVar_hsa_circ_223233,RMVar_hsa_circ_19716,RMVar_hsa_circ_223232,RMVar_hsa_circ_27637,RMVar_hsa_circ_84026,RMVar_hsa_circ_223230,RMVar_hsa_circ_223241,RMVar_hsa_circ_46402,RMVar_hsa_circ_223244,RMVar_hsa_circ_91678 2832 RMVar_ID_2832 Human_SNP_ID_166290516 A-to-I Human chr3 + 183796082 183796082 183796082 TCGGCCTACTGAAACCTCCGCCTCCCGAGTTCAAGTGATTTTCCTGCCTCAGCCTCCCAAGTAGC TCGGCCTACTGAAACCTCCGCCTCCCGAGTTCGAGTGATTTTCCTGCCTCAGCCTCCCAAGTAGC A G YEATS2 Ensembl:ENSG00000163872 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1291354935 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9195,RMVar_hsa_circ_74353,RMVar_hsa_circ_62303,RMVar_hsa_circ_114457,RMVar_hsa_circ_223176,RMVar_hsa_circ_76043,RMVar_hsa_circ_38709,RMVar_hsa_circ_8462,RMVar_hsa_circ_99840,RMVar_hsa_circ_120074,RMVar_hsa_circ_223183,RMVar_hsa_circ_103962,RMVar_hsa_circ_116923,RMVar_hsa_circ_86944,RMVar_hsa_circ_223191,RMVar_hsa_circ_18261,RMVar_hsa_circ_223193,RMVar_hsa_circ_223192,RMVar_hsa_circ_223190,RMVar_hsa_circ_377071,RMVar_hsa_circ_117039,RMVar_hsa_circ_223202,RMVar_hsa_circ_127150,RMVar_hsa_circ_223201,RMVar_hsa_circ_223209,RMVar_hsa_circ_111494,RMVar_hsa_circ_223210,RMVar_hsa_circ_28287,RMVar_hsa_circ_223208,RMVar_hsa_circ_5404,RMVar_hsa_circ_375753,RMVar_hsa_circ_127788,RMVar_hsa_circ_269810,RMVar_hsa_circ_44426,RMVar_hsa_circ_223222,RMVar_hsa_circ_223223,RMVar_hsa_circ_86919,RMVar_hsa_circ_117939,RMVar_hsa_circ_120439,RMVar_hsa_circ_110941,RMVar_hsa_circ_82475,RMVar_hsa_circ_40511,RMVar_hsa_circ_223231,RMVar_hsa_circ_85757,RMVar_hsa_circ_223224,RMVar_hsa_circ_223226,RMVar_hsa_circ_223228,RMVar_hsa_circ_223227,RMVar_hsa_circ_223225,RMVar_hsa_circ_275036,RMVar_hsa_circ_122357,RMVar_hsa_circ_90312,RMVar_hsa_circ_223233,RMVar_hsa_circ_19716,RMVar_hsa_circ_223232,RMVar_hsa_circ_27637,RMVar_hsa_circ_84026,RMVar_hsa_circ_223230,RMVar_hsa_circ_223241,RMVar_hsa_circ_46402,RMVar_hsa_circ_223244,RMVar_hsa_circ_91678 2833 RMVar_ID_2833 Human_SNP_ID_166297860 A-to-I Human chr3 - 183820598 183820598 183820598 ACTGTGCCTGGCCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGATGG ACTGTGCCTGGCCTAATTTTTGTATTTTTAGTGGAGACGGGGTTTCACCATGTTGGCCAGGATGG T C AC131160.1,MAP6D1 Ensembl:ENSG00000283765,Ensembl:ENSG00000180834 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs985436872 Functional Loss SNV dbSNP153 33..33 33 - - - 2834 RMVar_ID_2834 Human_SNP_ID_166313160 A-to-I Human chr3 - 183880932 183880932 183880932 TGCTGCCTCTGGTCCCAGCCACGTGGGAGGCTAAGGGAGGAGGATTGCTTGAGGCCGGAAGGTGA TGCTGCCTCTGGTCCCAGCCACGTGGGAGGCTGAGGGAGGAGGATTGCTTGAGGCCGGAAGGTGA T C AC131160.1,PARL Ensembl:ENSG00000283765,Ensembl:ENSG00000175193 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs992635348 Functional Loss SNV dbSNP153 33..33 33 - - - 2835 RMVar_ID_2835 Human_SNP_ID_166313363 A-to-I Human chr3 - 183881696 183881696 183881696 TGAAGTGCAGTGGCACTATCATAGCTCACTGCAGCCTCAAACTCCTGGGTTCAAGGGATCCCCCT TGAAGTGCAGTGGCACTATCATAGCTCACTGCTGCCTCAAACTCCTGGGTTCAAGGGATCCCCCT T A AC131160.1,PARL Ensembl:ENSG00000283765,Ensembl:ENSG00000175193 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1431894716 Functional Loss SNV dbSNP153 33..33 33 - - - 2836 RMVar_ID_2836 Human_SNP_ID_166313371 A-to-I Human chr3 - 183881725 183881725 183881725 TTAGAGGCGAGTTGTTCTGTCACCTAGGTTGAAGTGCAGTGGCACTATCATAGCTCACTGCAGCC TTAGAGGCGAGTTGTTCTGTCACCTAGGTTGACGTGCAGTGGCACTATCATAGCTCACTGCAGCC T G AC131160.1,PARL Ensembl:ENSG00000283765,Ensembl:ENSG00000175193 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs889697607 Functional Loss SNV dbSNP153 33..33 33 - - - 2837 RMVar_ID_2837 Human_SNP_ID_166328216 A-to-I Human chr3 - 183940387 183940387 183940387 GGTGCAATCTCGGCTCTGGAGTAGCTGGGATTACAGGCACATGCCACCATGCCCAGCTAATTTTT GGTGCAATCTCGGCTCTGGAGTAGCTGGGATTGCAGGCACATGCCACCATGCCCAGCTAATTTTT T C ABCC5 Ensembl:ENSG00000114770 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1442961630 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55450,RMVar_hsa_circ_268239,RMVar_hsa_circ_73450,RMVar_hsa_circ_26084,RMVar_hsa_circ_51698,RMVar_hsa_circ_376529,RMVar_hsa_circ_311921,RMVar_hsa_circ_339205,RMVar_hsa_circ_121090,RMVar_hsa_circ_223275,RMVar_hsa_circ_223276,RMVar_hsa_circ_223277 2838 RMVar_ID_2838 Human_SNP_ID_166328573 A-to-I Human chr3 - 183941740 183941740 183941740 GACCTCATGATCCACCCGCCTCAGCCTCTGAAAGTGCTGGGATTACAGGTGTGAGCCATCGCACC GACCTCATGATCCACCCGCCTCAGCCTCTGAACGTGCTGGGATTACAGGTGTGAGCCATCGCACC T G ABCC5 Ensembl:ENSG00000114770 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1305171279 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55450,RMVar_hsa_circ_268239,RMVar_hsa_circ_73450,RMVar_hsa_circ_26084,RMVar_hsa_circ_51698,RMVar_hsa_circ_376529,RMVar_hsa_circ_311921,RMVar_hsa_circ_339205,RMVar_hsa_circ_121090,RMVar_hsa_circ_223275,RMVar_hsa_circ_223276,RMVar_hsa_circ_223277 2839 RMVar_ID_2839 Human_SNP_ID_166346383 A-to-I Human chr3 - 184014328 184014328 184014328 CATCCCCAGTCCTGGGTATAGAAGTGTGAGGGAGAGAACCAGCACTTCTGGGACGCACAGAGACC CATCCCCAGTCCTGGGTATAGAAGTGTGAGGGGGAGAACCAGCACTTCTGGGACGCACAGAGACC T C ABCC5 Ensembl:ENSG00000114770 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1372270633 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_938727,Human_RBP_ID_3965727,Human_RBP_ID_9394288,Human_RBP_ID_19011093 Human_Splice_Rec_514273,Human_Splice_Rec_514329,Human_Splice_Rec_514383,Human_Splice_Rec_514461,Human_Splice_Rec_514469,Human_Splice_Rec_514481,Human_Splice_Rec_514491,Human_Splice_Rec_514503,Human_Splice_Rec_514511,Human_Splice_Rec_514517 RMVar_hsa_circ_340383,RMVar_hsa_circ_321698,RMVar_hsa_circ_62606,RMVar_hsa_circ_13777,RMVar_hsa_circ_105051,RMVar_hsa_circ_223286,RMVar_hsa_circ_310069 2840 RMVar_ID_2840 Human_SNP_ID_166378335 A-to-I Human chr3 + 184139481 184139481 184139481 TTTTGTATTTTTAGTAGAGACGAGGTTTTACCATGTTGGTCAGGCTGGTCTCGAACTCCCAACCT TTTTGTATTTTTAGTAGAGACGAGGTTTTACCCTGTTGGTCAGGCTGGTCTCGAACTCCCAACCT A C EIF2B5 Ensembl:ENSG00000145191 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs368541880 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_223287,RMVar_hsa_circ_73420,RMVar_hsa_circ_375025 2841 RMVar_ID_2841 Human_SNP_ID_166381056 A-to-I Human chr3 + 184149740 184149740 184149740 CTGTGCAAATTTCCAAGAAGAGGATGTTTGTCACTGATGACATCTTCAAAGCTGAACTGAATGAG CTGTGCAAATTTCCAAGAAGAGGATGTTTGTCGCTGATGACATCTTCAAAGCTGAACTGAATGAG A G AC131235.2 Ensembl:ENSG00000228205 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879144109 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1885499 2842 RMVar_ID_2842 Human_SNP_ID_166381059 A-to-I Human chr3 + 184149747 184149747 184149747 AATTTCCAAGAAGAGGATGTTTGTCACTGATGACATCTTCAAAGCTGAACTGAATGAGTTTCTTA AATTTCCAAGAAGAGGATGTTTGTCACTGATGGCATCTTCAAAGCTGAACTGAATGAGTTTCTTA A G AC131235.2 Ensembl:ENSG00000228205 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878876281 Functional Loss SNV dbSNP153 33..33 33 - - - 2843 RMVar_ID_2843 Human_SNP_ID_166381103 A-to-I Human chr3 + 184149917 184149917 184149917 AGAAGGGCTGACGGATTCGGGAACTGACTGCTATAGTTCAGAAGAGGTTTGGCTTTCCAGAGGGC AGAAGGGCTGACGGATTCGGGAACTGACTGCTGTAGTTCAGAAGAGGTTTGGCTTTCCAGAGGGC A G AC131235.2 Ensembl:ENSG00000228205 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879049998 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_596384,Human_RBP_ID_1064071,Human_RBP_ID_1957355,Human_RBP_ID_2770747,Human_RBP_ID_5602230,Human_RBP_ID_7167503,Human_RBP_ID_8566924,Human_RBP_ID_9137056,Human_RBP_ID_10113394,Human_RBP_ID_26505968 Human_miRNA_ID_1898764 2844 RMVar_ID_2844 Human_SNP_ID_166381223 A-to-I Human chr3 - 184150426 184150426 184150426 ATACAGCTGCTAAGGAGACCCTGTTATGCTGTAGGGACTGGCTGGGGCATGGCAGATGGCTCTGG ATACAGCTGCTAAGGAGACCCTGTTATGCTGTGGGGACTGGCTGGGGCATGGCAGATGGCTCTGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879076759 Functional Loss SNV dbSNP153 33..33 33 - - - 2845 RMVar_ID_2845 Human_SNP_ID_166381228 A-to-I Human chr3 + 184150448 184150448 184150448 AGCCAGTCCCTACAGCATAACAGGGTCTCCTTAGCAGCTGTATTCTGGAGTCTGGATGTTGCTCT AGCCAGTCCCTACAGCATAACAGGGTCTCCTTGGCAGCTGTATTCTGGAGTCTGGATGTTGCTCT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879003407 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_596399,Human_RBP_ID_26511923 2846 RMVar_ID_2846 Human_SNP_ID_166384134 A-to-I Human chr3 + 184161613 184161613 184161613 CCTCAAACTTTTCCACTCCCCTTCCTAGCCCCAAACTGTAGTTACTGCCTGACTTCTTGCCTCAC CCTCAAACTTTTCCACTCCCCTTCCTAGCCCCGAACTGTAGTTACTGCCTGACTTCTTGCCTCAC A G DVL3 Ensembl:ENSG00000161202 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1395668294 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83566,RMVar_hsa_circ_223293 2847 RMVar_ID_2847 Human_SNP_ID_166384135 A-to-I Human chr3 + 184161614 184161614 184161614 CTCAAACTTTTCCACTCCCCTTCCTAGCCCCAAACTGTAGTTACTGCCTGACTTCTTGCCTCACC CTCAAACTTTTCCACTCCCCTTCCTAGCCCCAGACTGTAGTTACTGCCTGACTTCTTGCCTCACC A G DVL3 Ensembl:ENSG00000161202 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1399873886 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83566,RMVar_hsa_circ_223293 2848 RMVar_ID_2848 Human_SNP_ID_166384147 A-to-I Human chr3 + 184161666 184161666 184161666 TTCTTGCCTCACCACATTCCCCCGGCCAAACTACATGCTCCGTGACCACATTCCACACCCTTCAT TTCTTGCCTCACCACATTCCCCCGGCCAAACTCCATGCTCCGTGACCACATTCCACACCCTTCAT A C DVL3 Ensembl:ENSG00000161202 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1322700063 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83566,RMVar_hsa_circ_223293 2849 RMVar_ID_2849 Human_SNP_ID_166390348 A-to-I Human chr3 + 184183771 184183771 184183771 GCCCGAGTCTAGGTCTGGGCCAAGCACATTACAAGTGGGACCGGTGGAGCAGCCCCTGGGCTCCC GCCCGAGTCTAGGTCTGGGCCAAGCACATTACCAGTGGGACCGGTGGAGCAGCCCCTGGGCTCCC A C AP2M1 Ensembl:ENSG00000161203 Protein coding 3'UTR GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs748545110 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_68188,Human_RBP_ID_596498,Human_RBP_ID_1032224,Human_RBP_ID_1623257,Human_RBP_ID_4763162,Human_RBP_ID_8566985,Human_RBP_ID_17289343,Human_RBP_ID_17402735,Human_RBP_ID_17518749,Human_RBP_ID_17661592,Human_RBP_ID_18194749,Human_RBP_ID_27500179 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 2850 RMVar_ID_2850 Human_SNP_ID_166394189 A-to-I Human chr3 + 184195198 184195197 184195199 TCAGCCTGGGCGACAGAGCGAGACTTCTTCTCAAGAAAAAAAAAAAAAAAGCTTGACCAAAGAAT TCAGCCTGGGCGACAGAGCGAGACTTCTTCTC__GAAAAAAAAAAAAAAAGCTTGACCAAAGAAT CAA C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1489652401 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_18001174 2851 RMVar_ID_2851 Human_SNP_ID_166394638 A-to-I Human chr3 + 184197042 184197042 184197042 CAGAGTGGAGTGCAGTGGCGCGATCTCAGTTCACTGCAACCTCTGTCTCCCAGGTTCAAGAGATT CAGAGTGGAGTGCAGTGGCGCGATCTCAGTTCGCTGCAACCTCTGTCTCCCAGGTTCAAGAGATT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1227236166 Functional Loss SNV dbSNP153 33..33 33 - - - 2852 RMVar_ID_2852 Human_SNP_ID_166395014 A-to-I Human chr3 + 184198141 184198141 184198141 CAGGCTGGAGTGCAGTGGCGCGATCTCTGCTCACTGCAAGCTCTGCCTCACGGGTTCATGCCATT CAGGCTGGAGTGCAGTGGCGCGATCTCTGCTCGCTGCAAGCTCTGCCTCACGGGTTCATGCCATT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1464670029 Functional Loss SNV dbSNP153 33..33 33 - - - 2853 RMVar_ID_2853 Human_SNP_ID_166429097 A-to-I Human chr3 + 184318684 184318684 184318684 TGGAATGTAGTCGCACAGTCTTGGCTCTCTGCAGCCTCCGCCTCTTGGGTTCAAGTGATTCTCCT TGGAATGTAGTCGCACAGTCTTGGCTCTCTGCGGCCTCCGCCTCTTGGGTTCAAGTGATTCTCCT A G EIF4G1 Ensembl:ENSG00000114867 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1213643927 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14745212 RMVar_hsa_circ_111936,RMVar_hsa_circ_223366,RMVar_hsa_circ_89072,RMVar_hsa_circ_49400,RMVar_hsa_circ_223369,RMVar_hsa_circ_98865,RMVar_hsa_circ_66240,RMVar_hsa_circ_223371 2854 RMVar_ID_2854 Human_SNP_ID_166432868 A-to-I Human chr3 + 184329460 184329460 184329460 CAAGACCAGCTTGGCCAATATGGTGAAACCCCATCTCTACTAAAAACACAAAAATTAGCCGTGTT CAAGACCAGCTTGGCCAATATGGTGAAACCCCGTCTCTACTAAAAACACAAAAATTAGCCGTGTT A G EIF4G1 Ensembl:ENSG00000114867 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1965451 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105927,RMVar_hsa_circ_223373,RMVar_hsa_circ_223376,RMVar_hsa_circ_109512 2855 RMVar_ID_2855 Human_SNP_ID_166433292 A-to-I Human chr3 + 184331008 184331008 184331008 GTGATCCGCCCACCTCGACCTTTCAGAGTGCTAGGATTACAGGCGTGAGCCACCGCCCGCTCCTG GTGATCCGCCCACCTCGACCTTTCAGAGTGCTGGGATTACAGGCGTGAGCCACCGCCCGCTCCTG A G EIF4G1 Ensembl:ENSG00000114867 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1277915803 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14745352,Human_RBP_ID_23188863 RMVar_hsa_circ_105927,RMVar_hsa_circ_223373,RMVar_hsa_circ_223376,RMVar_hsa_circ_109512 2856 RMVar_ID_2856 Human_SNP_ID_166443134 A-to-I Human chr3 + 184363952 184363952 184363952 GGGCGCCTGTAATCCCAGCTACTTGGGAGGCTAAGGCAGGAGAATTGCCTGAACCTGGGAGGCGG GGGCGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATTGCCTGAACCTGGGAGGCGG A G POLR2H Ensembl:ENSG00000163882 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1004466198 Functional Loss SNV dbSNP153 33..33 33 - - - 2857 RMVar_ID_2857 Human_SNP_ID_166443147 A-to-I Human chr3 + 184363992 184363992 184363992 AGAATTGCCTGAACCTGGGAGGCGGAGGTTGCAGTGAGCCAAGATCGCGCCACTGCACGCCAGCC AGAATTGCCTGAACCTGGGAGGCGGAGGTTGCCGTGAGCCAAGATCGCGCCACTGCACGCCAGCC A C POLR2H Ensembl:ENSG00000163882 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1281300215 Functional Loss SNV dbSNP153 33..33 33 - - - 2858 RMVar_ID_2858 Human_SNP_ID_166533791 A-to-I Human chr3 - 184703494 184703494 184703494 GTTGTTGCCCACGCTGGACATGATCTCGGCTCACTGCAACCTCTGCCTCCCAGGTTCAAGCAATT GTTGTTGCCCACGCTGGACATGATCTCGGCTCGCTGCAACCTCTGCCTCCCAGGTTCAAGCAATT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1249102347 Functional Loss SNV dbSNP153 33..33 33 - - - 2859 RMVar_ID_2859 Human_SNP_ID_166533804 A-to-I Human chr3 - 184703534 184703534 184703534 AGGGTTTTATTTTATTTATTTATTTTTGAGACAGAGTCTCGTTGTTGCCCACGCTGGACATGATC AGGGTTTTATTTTATTTATTTATTTTTGAGACGGAGTCTCGTTGTTGCCCACGCTGGACATGATC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1322357294 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7168110,Human_RBP_ID_8567257 2860 RMVar_ID_2860 Human_SNP_ID_166571192 A-to-I Human chr3 + 184848140 184848140 184848140 CACTGTGTTGGCCAGGCTGGTCTCGAACTCCTAACCTCAAGTGACCTTCCCTTCCTCAGCCTCCC CACTGTGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAAGTGACCTTCCCTTCCTCAGCCTCCC A G VPS8 Ensembl:ENSG00000156931 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1034507164 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25720304 RMVar_hsa_circ_1837,RMVar_hsa_circ_61767,RMVar_hsa_circ_35692,RMVar_hsa_circ_57688,RMVar_hsa_circ_356094,RMVar_hsa_circ_371523,RMVar_hsa_circ_360288,RMVar_hsa_circ_355721,RMVar_hsa_circ_277557,RMVar_hsa_circ_73852,RMVar_hsa_circ_38910,RMVar_hsa_circ_45510,RMVar_hsa_circ_41526,RMVar_hsa_circ_10562,RMVar_hsa_circ_24465,RMVar_hsa_circ_7853,RMVar_hsa_circ_43155,RMVar_hsa_circ_13765,RMVar_hsa_circ_223390,RMVar_hsa_circ_223392,RMVar_hsa_circ_223391,RMVar_hsa_circ_27754,RMVar_hsa_circ_64470,RMVar_hsa_circ_223396,RMVar_hsa_circ_339470,RMVar_hsa_circ_377356,RMVar_hsa_circ_43519,RMVar_hsa_circ_114398,RMVar_hsa_circ_273290,RMVar_hsa_circ_51665,RMVar_hsa_circ_223397,RMVar_hsa_circ_223398 2861 RMVar_ID_2861 Human_SNP_ID_166598642 A-to-I Human chr3 + 184967131 184967131 184967131 TGGGACTACAGGCGTATGCCATCACATTGGCTAATTTCTGTATTTTTTGTAGAGATGGGGTTTCA TGGGACTACAGGCGTATGCCATCACATTGGCTGATTTCTGTATTTTTTGTAGAGATGGGGTTTCA A G VPS8 Ensembl:ENSG00000156931 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1296870135 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5237,RMVar_hsa_circ_57688,RMVar_hsa_circ_73852,RMVar_hsa_circ_45510,RMVar_hsa_circ_7853,RMVar_hsa_circ_295408,RMVar_hsa_circ_27754,RMVar_hsa_circ_43519,RMVar_hsa_circ_51665,RMVar_hsa_circ_293308,RMVar_hsa_circ_280060,RMVar_hsa_circ_13832,RMVar_hsa_circ_223399,RMVar_hsa_circ_365358,RMVar_hsa_circ_37745,RMVar_hsa_circ_327821,RMVar_hsa_circ_336889,RMVar_hsa_circ_31953,RMVar_hsa_circ_223418,RMVar_hsa_circ_22048,RMVar_hsa_circ_223432,RMVar_hsa_circ_335502,RMVar_hsa_circ_92011,RMVar_hsa_circ_363693,RMVar_hsa_circ_53330,RMVar_hsa_circ_70946,RMVar_hsa_circ_223426,RMVar_hsa_circ_223427,RMVar_hsa_circ_372985,RMVar_hsa_circ_295527,RMVar_hsa_circ_319896,RMVar_hsa_circ_283176,RMVar_hsa_circ_223433,RMVar_hsa_circ_291966,RMVar_hsa_circ_335101,RMVar_hsa_circ_223431,RMVar_hsa_circ_354681,RMVar_hsa_circ_316100,RMVar_hsa_circ_285925,RMVar_hsa_circ_270956,RMVar_hsa_circ_35966,RMVar_hsa_circ_223435,RMVar_hsa_circ_223436,RMVar_hsa_circ_223439,RMVar_hsa_circ_223434,RMVar_hsa_circ_375436,RMVar_hsa_circ_306120,RMVar_hsa_circ_320940,RMVar_hsa_circ_277190,RMVar_hsa_circ_223440,RMVar_hsa_circ_223441 2862 RMVar_ID_2862 Human_SNP_ID_166721156 A-to-I Human chr3 - 185481296 185481296 185481296 TGTTGTTGTTGTTGTAGAGGCAAGGTCTTGCTATGTTGCTCAGACTGATCTTGAACTCCTGACCC TGTTGTTGTTGTTGTAGAGGCAAGGTCTTGCTTTGTTGCTCAGACTGATCTTGAACTCCTGACCC T A TMEM41A Ensembl:ENSG00000163900 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs925277821 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25720704 Human_Splice_Rec_519872,Human_Splice_Rec_519873 2863 RMVar_ID_2863 Human_SNP_ID_166721157 A-to-I Human chr3 - 185481296 185481296 185481296 TGTTGTTGTTGTTGTAGAGGCAAGGTCTTGCTATGTTGCTCAGACTGATCTTGAACTCCTGACCC TGTTGTTGTTGTTGTAGAGGCAAGGTCTTGCTGTGTTGCTCAGACTGATCTTGAACTCCTGACCC T C TMEM41A Ensembl:ENSG00000163900 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs925277821 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25720704 Human_Splice_Rec_519872,Human_Splice_Rec_519873 2864 RMVar_ID_2864 Human_SNP_ID_166723399 A-to-I Human chr3 - 185491180 185491177 185491181 CAGCCTGGCCAAGATGGTGAAATCCTGTCTCTAATAAAAATACAAAAATTAGCCAGGCGTGGTGG CAGCCTGGCCAAGATGGTGAAATCCTGTCTC____AAAAATACAAAAATTAGCCAGGCGTGGTGG TATTA T TMEM41A Ensembl:ENSG00000163900 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1366063210 Functional Loss DEL dbSNP153 32..35 33 - - - RMVar_hsa_circ_92721,RMVar_hsa_circ_94072,RMVar_hsa_circ_86747,RMVar_hsa_circ_90806,RMVar_hsa_circ_223478,RMVar_hsa_circ_223480,RMVar_hsa_circ_223481,RMVar_hsa_circ_223479 2865 RMVar_ID_2865 Human_SNP_ID_166723651 A-to-I Human chr3 - 185492110 185492110 185492110 TTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGATCTCGAACTCCTGACCTCAGGTGATC TTTAGTAGAGACGGGGTTTCACCATGTTGGCCGGGCTGATCTCGAACTCCTGACCTCAGGTGATC T C TMEM41A Ensembl:ENSG00000163900 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1306774442 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92721,RMVar_hsa_circ_94072,RMVar_hsa_circ_86747,RMVar_hsa_circ_223480,RMVar_hsa_circ_223481,RMVar_hsa_circ_223479 2866 RMVar_ID_2866 Human_SNP_ID_166723988 A-to-I Human chr3 - 185493638 185493638 185493638 ACTTGGGAGGCTGAGGCAGGAGAATGGCTTGAACCTGGGAGGCGGAGGTTGCAGTAAGCTGAGAG ACTTGGGAGGCTGAGGCAGGAGAATGGCTTGACCCTGGGAGGCGGAGGTTGCAGTAAGCTGAGAG T G TMEM41A Ensembl:ENSG00000163900 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1276106151 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92721,RMVar_hsa_circ_94072,RMVar_hsa_circ_86747,RMVar_hsa_circ_223480,RMVar_hsa_circ_223481,RMVar_hsa_circ_223479 2867 RMVar_ID_2867 Human_SNP_ID_166723997 A-to-I Human chr3 - 185493670 185493670 185493670 CTGACATGGTGGTGTGCGTCTGTAATTCAACTACTTGGGAGGCTGAGGCAGGAGAATGGCTTGAA CTGACATGGTGGTGTGCGTCTGTAATTCAACTGCTTGGGAGGCTGAGGCAGGAGAATGGCTTGAA T C TMEM41A Ensembl:ENSG00000163900 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs993053409 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25720723 RMVar_hsa_circ_92721,RMVar_hsa_circ_94072,RMVar_hsa_circ_86747,RMVar_hsa_circ_223480,RMVar_hsa_circ_223481,RMVar_hsa_circ_223479 2868 RMVar_ID_2868 Human_SNP_ID_166757154 A-to-I Human chr3 + 185623661 185623661 185623661 CCTGGCTAACACGGTGAAACCCCATCTCTACTAAGAAAAATACAAAAAATTAGCAGGGCGTGGTG CCTGGCTAACACGGTGAAACCCCATCTCTACTGAGAAAAATACAAAAAATTAGCAGGGCGTGGTG A G SENP2 Ensembl:ENSG00000163904 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1354758191 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33061,RMVar_hsa_circ_314516,RMVar_hsa_circ_223490,RMVar_hsa_circ_223494,RMVar_hsa_circ_289272,RMVar_hsa_circ_269088,RMVar_hsa_circ_56916,RMVar_hsa_circ_223500,RMVar_hsa_circ_312516,RMVar_hsa_circ_66841,RMVar_hsa_circ_223495,RMVar_hsa_circ_358979,RMVar_hsa_circ_325270,RMVar_hsa_circ_106829,RMVar_hsa_circ_358036,RMVar_hsa_circ_223503,RMVar_hsa_circ_223501,RMVar_hsa_circ_287496,RMVar_hsa_circ_334676,RMVar_hsa_circ_223502,RMVar_hsa_circ_315357,RMVar_hsa_circ_316000,RMVar_hsa_circ_223505,RMVar_hsa_circ_328439,RMVar_hsa_circ_310160,RMVar_hsa_circ_351061,RMVar_hsa_circ_270416 2869 RMVar_ID_2869 Human_SNP_ID_166761698 A-to-I Human chr3 - 185638784 185638784 185638784 CAGGGTTCCACCATGTTGGCCAAACTGGTCTCAAACACCTGACCTCAGGTGATCCTCCCGCCTCG CAGGGTTCCACCATGTTGGCCAAACTGGTCTCGAACACCTGACCTCAGGTGATCCTCCCGCCTCG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1411220986 Functional Loss SNV dbSNP153 33..33 33 - - - 2870 RMVar_ID_2870 Human_SNP_ID_166767101 A-to-I Human chr3 - 185659018 185659018 185659018 TACAGATGGGATCTCTCTGTGTCACCCAGGCTAGTCTCAAGTTCCTGAACCCAAGTGATCCTCCC TACAGATGGGATCTCTCTGTGTCACCCAGGCTTGTCTCAAGTTCCTGAACCCAAGTGATCCTCCC T A IGF2BP2 Ensembl:ENSG00000073792 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1214685162 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17573931 RMVar_hsa_circ_9180,RMVar_hsa_circ_50549,RMVar_hsa_circ_95113,RMVar_hsa_circ_33451,RMVar_hsa_circ_223508,RMVar_hsa_circ_61968,RMVar_hsa_circ_312972,RMVar_hsa_circ_223509 2871 RMVar_ID_2871 Human_SNP_ID_166770575 A-to-I Human chr3 - 185671354 185671354 185671354 TTTAGTAGAGAAGGGGTTTCACCATGTTGGCCAGGATGGTCTCCATCTCCTGACCTCGTGATCTG TTTAGTAGAGAAGGGGTTTCACCATGTTGGCCGGGATGGTCTCCATCTCCTGACCTCGTGATCTG T C IGF2BP2 Ensembl:ENSG00000073792 Protein coding intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs967336568 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9180,RMVar_hsa_circ_50549,RMVar_hsa_circ_95113,RMVar_hsa_circ_33451,RMVar_hsa_circ_223508,RMVar_hsa_circ_61968,RMVar_hsa_circ_312972,RMVar_hsa_circ_223509 2872 RMVar_ID_2872 Human_SNP_ID_166838864 A-to-I Human chr3 - 185938001 185938001 185938001 CGTCACATCCGGTAGAGTTAGAGCCCGTGCGGAGGCGGTGCGGAGCATTTCGGCTCTGAGCGGCT CGTCACATCCGGTAGAGTTAGAGCCCGTGCGGTGGCGGTGCGGAGCATTTCGGCTCTGAGCGGCT T A TRA2B Ensembl:ENSG00000136527 Protein coding 5'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs531991062 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4757619,Human_RBP_ID_18424111 RMVar_hsa_circ_116021,RMVar_hsa_circ_223534 2873 RMVar_ID_2873 Human_SNP_ID_166838865 A-to-I Human chr3 - 185938001 185938001 185938001 CGTCACATCCGGTAGAGTTAGAGCCCGTGCGGAGGCGGTGCGGAGCATTTCGGCTCTGAGCGGCT CGTCACATCCGGTAGAGTTAGAGCCCGTGCGGCGGCGGTGCGGAGCATTTCGGCTCTGAGCGGCT T G TRA2B Ensembl:ENSG00000136527 Protein coding 5'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs531991062 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4757619,Human_RBP_ID_18424111 RMVar_hsa_circ_116021,RMVar_hsa_circ_223534 2874 RMVar_ID_2874 Human_SNP_ID_166847732 A-to-I Human chr3 + 185972399 185972399 185972399 TTAAATAGATACGGGGTTTCACCATGTTGCCCAGGCTAGTCTCAAACTCCTGAACTCAAGGGATC TTAAATAGATACGGGGTTTCACCATGTTGCCCTGGCTAGTCTCAAACTCCTGAACTCAAGGGATC A T NMRAL2P Ensembl:ENSG00000171658 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs764870742 Functional Loss SNV dbSNP153 33..33 33 - - - 2875 RMVar_ID_2875 Human_SNP_ID_166848163 A-to-I Human chr3 + 185973995 185973995 185973995 TTGGGAGGCCAAGGCAGGCGGATCACGAGGTCAGGAGATTGAGACCATCTTGGCTAACACGGTGA TTGGGAGGCCAAGGCAGGCGGATCACGAGGTCGGGAGATTGAGACCATCTTGGCTAACACGGTGA A G NMRAL2P Ensembl:ENSG00000171658 Pseudogene intron GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs1213078852 Functional Loss SNV dbSNP153 33..33 33 - - - 2876 RMVar_ID_2876 Human_SNP_ID_166848203 A-to-I Human chr3 + 185974163 185974163 185974163 AGGAGGCGGAGCTTGCAGTGAGCAGAAATCGCACCACTGCACTCCAGCCTGGGTGAAAGTGCAAG AGGAGGCGGAGCTTGCAGTGAGCAGAAATCGCCCCACTGCACTCCAGCCTGGGTGAAAGTGCAAG A C NMRAL2P Ensembl:ENSG00000171658 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs906429150 Functional Loss SNV dbSNP153 33..33 33 - - - 2877 RMVar_ID_2877 Human_SNP_ID_166849869 A-to-I Human chr3 + 185981001 185981001 185981001 ATCGCCTGAGCCCAGGAGTTTAAGACTAGCCTAGGCAACATGGTGAGACCCTCTCTCTGGAAAAA ATCGCCTGAGCCCAGGAGTTTAAGACTAGCCTGGGCAACATGGTGAGACCCTCTCTCTGGAAAAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1560028820 Functional Loss SNV dbSNP153 33..33 33 - - - 2878 RMVar_ID_2878 Human_SNP_ID_166850191 A-to-I Human chr3 + 185982270 185982270 185982270 CTCCTGCCTCCACCTCCTGAGTAGCTGGGACTACAGGCACATAGTACCATGCCCGGCTAATTCTT CTCCTGCCTCCACCTCCTGAGTAGCTGGGACTGCAGGCACATAGTACCATGCCCGGCTAATTCTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749253827 Functional Loss SNV dbSNP153 33..33 33 - - - 2879 RMVar_ID_2879 Human_SNP_ID_166850224 A-to-I Human chr3 + 185982402 185982402 185982402 AAACTTCTGGCCTCAAGCTATCTGCCTGCCTCAGCCTCCCAAAGTGTTGGGATTACAGGCATGAG AAACTTCTGGCCTCAAGCTATCTGCCTGCCTCCGCCTCCCAAAGTGTTGGGATTACAGGCATGAG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1178266875 Functional Loss SNV dbSNP153 33..33 33 - - - 2880 RMVar_ID_2880 Human_SNP_ID_166850531 A-to-I Human chr3 + 185983415 185983415 185983415 TTTGGTGGAGACAGGGTTTCTCCATGTTGGTCAGGCTGGTCTCGAACTACTGACCTTAGGTGATC TTTGGTGGAGACAGGGTTTCTCCATGTTGGTCGGGCTGGTCTCGAACTACTGACCTTAGGTGATC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1267440527 Functional Loss SNV dbSNP153 33..33 33 - - - 2881 RMVar_ID_2881 Human_SNP_ID_166988254 A-to-I Human chr3 - 186547454 186547454 186547454 GCCAGGAGTTTGAGACCAGCCTGGGCAATATAATGAGACCCTGTCTCTACAAAAAAATTAAAAAT GCCAGGAGTTTGAGACCAGCCTGGGCAATATATTGAGACCCTGTCTCTACAAAAAAATTAAAAAT T A TBCCD1 Ensembl:ENSG00000113838 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1004575089 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_223559,RMVar_hsa_circ_89642 2882 RMVar_ID_2882 Human_SNP_ID_166995569 A-to-I Human chr3 + 186575864 186575864 186575864 ATCCCCAGGTTCTGTCAGATAGTGAGAAACGGAAACAGTACGATACTTATGGTGAAGAAGGATTA ATCCCCAGGTTCTGTCAGATAGTGAGAAACGGCAACAGTACGATACTTATGGTGAAGAAGGATTA A C DNAJB11 Ensembl:ENSG00000090520 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1376809675 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_66805,Human_RBP_ID_9348653,Human_RBP_ID_14752761,Human_RBP_ID_18013043,Human_RBP_ID_23990730 Human_Splice_Rec_521172,Human_Splice_Rec_521173,Human_Splice_Rec_521190,Human_Splice_Rec_521191,Human_Splice_Rec_521206,Human_Splice_Rec_521207 Human_miRNA_ID_2647158,Human_miRNA_ID_2669751,Human_miRNA_ID_2718832,Human_miRNA_ID_3100399 RMVar_hsa_circ_86211,RMVar_hsa_circ_99814,RMVar_hsa_circ_223561,RMVar_hsa_circ_223562 2883 RMVar_ID_2883 Human_SNP_ID_167056314 A-to-I Human chr3 - 186804126 186804126 186804126 CAGGCTGGCGTGCAGTGGCATGGTCTCGACTCACTGCAACCTCCACCTCCTGGGTTCAGGTGATT CAGGCTGGCGTGCAGTGGCATGGTCTCGACTCTCTGCAACCTCCACCTCCTGGGTTCAGGTGATT T A RFC4 Ensembl:ENSG00000163918 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1291980325 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58528,RMVar_hsa_circ_223590,RMVar_hsa_circ_75940,RMVar_hsa_circ_274551,RMVar_hsa_circ_223593,RMVar_hsa_circ_296187,RMVar_hsa_circ_335678,RMVar_hsa_circ_223596,RMVar_hsa_circ_334541 2884 RMVar_ID_2884 Human_SNP_ID_167106624 A-to-I Human chr3 + 186995776 186995744 186995776 TGAGGCAGGAGAATAGCTTGAGCCCGGGAGGCAGAGGCTGCAGTGAGCCGAGATTGTGCCACTGT T________________________________GAGGCTGCAGTGAGCCGAGATTGTGCCACTGT TGAGGCAGGAGAATAGCTTGAGCCCGGGAGGCA T ST6GAL1 Ensembl:ENSG00000073849 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335915482 Functional Loss DEL dbSNP153 2..33 33 - - - RMVar_hsa_circ_223604,RMVar_hsa_circ_292669,RMVar_hsa_circ_327585,RMVar_hsa_circ_223606,RMVar_hsa_circ_276766,RMVar_hsa_circ_223605,RMVar_hsa_circ_223603 2885 RMVar_ID_2885 Human_SNP_ID_167138390 A-to-I Human chr3 - 187128621 187128621 187128621 CCTGTAGTCCCAGCTATTCAGGAGACTGAGGCAGGAGGATTACTCGAGGCCAGGCATTTGAGGCT CCTGTAGTCCCAGCTATTCAGGAGACTGAGGCCGGAGGATTACTCGAGGCCAGGCATTTGAGGCT T G RPL39L Ensembl:ENSG00000163923 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1248541907 Functional Loss SNV dbSNP153 33..33 33 - - - 2886 RMVar_ID_2886 Human_SNP_ID_167404012 A-to-I Human chr3 + 188189277 188189277 188189277 CCCAGCTAAGTTTTGTATTTTTTAATAGTGACAGGGTTTCACCATGTTTCCCAGGCTGGTCTCAA CCCAGCTAAGTTTTGTATTTTTTAATAGTGACCGGGTTTCACCATGTTTCCCAGGCTGGTCTCAA A C LPP Ensembl:ENSG00000145012 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1295456654 Functional Loss SNV dbSNP153 33..33 33 - - - 2887 RMVar_ID_2887 Human_SNP_ID_167404033 A-to-I Human chr3 + 188189362 188189362 188189362 CTCCTACCTTGGCCTCCCAAAGCACTGGCATTACAGGCATGAGCCACCGCACTAGGCCCATAAGG CTCCTACCTTGGCCTCCCAAAGCACTGGCATTGCAGGCATGAGCCACCGCACTAGGCCCATAAGG A G LPP Ensembl:ENSG00000145012 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1331922418 Functional Loss SNV dbSNP153 33..33 33 - - - 2888 RMVar_ID_2888 Human_SNP_ID_167406495 A-to-I Human chr3 + 188200349 188200349 188200349 GCGGCTCACCGCAACCTCTGCCTCCCAGGTTCAAGAGATTCTCCTGTCTCAGCCTCCCGAGTAAC GCGGCTCACCGCAACCTCTGCCTCCCAGGTTCCAGAGATTCTCCTGTCTCAGCCTCCCGAGTAAC A C LPP Ensembl:ENSG00000145012 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1359337598 Functional Loss SNV dbSNP153 33..33 33 - - - 2889 RMVar_ID_2889 Human_SNP_ID_167411081 A-to-I Human chr3 + 188219019 188219018 188219019 TGTTGACAAATCCAGATTTAGATCACTTTACCAGGAAGATGGGGCAGTTTTTATACTACCCTTTC TGTTGACAAATCCAGATTTAGATCACTTTACC_GGAAGATGGGGCAGTTTTTATACTACCCTTTC CA C LPP Ensembl:ENSG00000145012 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1205183379 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_119938,RMVar_hsa_circ_223622 2890 RMVar_ID_2890 Human_SNP_ID_167411082 A-to-I Human chr3 + 188219019 188219019 188219019 TGTTGACAAATCCAGATTTAGATCACTTTACCAGGAAGATGGGGCAGTTTTTATACTACCCTTTC TGTTGACAAATCCAGATTTAGATCACTTTACCCGGAAGATGGGGCAGTTTTTATACTACCCTTTC A C LPP Ensembl:ENSG00000145012 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1349069935 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119938,RMVar_hsa_circ_223622 2891 RMVar_ID_2891 Human_SNP_ID_167413648 A-to-I Human chr3 + 188230569 188230569 188230569 ACTTTGGGAGGCTGAGGCAGGCAGATCACCTGAGGTCGGGAGTTCAAGACCAGACTGACCAAAAT ACTTTGGGAGGCTGAGGCAGGCAGATCACCTGGGGTCGGGAGTTCAAGACCAGACTGACCAAAAT A G LPP Ensembl:ENSG00000145012 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs778108634 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41507,RMVar_hsa_circ_119938,RMVar_hsa_circ_312627,RMVar_hsa_circ_369433,RMVar_hsa_circ_223622,RMVar_hsa_circ_363337,RMVar_hsa_circ_223623 2892 RMVar_ID_2892 Human_SNP_ID_167413657 A-to-I Human chr3 + 188230628 188230628 188230628 CAAAATGGAGAAGCCTCATCTCTACTAGAAATACAAAATTAGCCGGGCATGCCTCTAATCCCAGC CAAAATGGAGAAGCCTCATCTCTACTAGAAATGCAAAATTAGCCGGGCATGCCTCTAATCCCAGC A G LPP Ensembl:ENSG00000145012 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1023430042 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41507,RMVar_hsa_circ_119938,RMVar_hsa_circ_312627,RMVar_hsa_circ_369433,RMVar_hsa_circ_223622,RMVar_hsa_circ_363337,RMVar_hsa_circ_223623 2893 RMVar_ID_2893 Human_SNP_ID_167421500 A-to-I Human chr3 + 188260924 188260924 188260924 GGGCGTGGTGGTGCATGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGTCAGGAGAATCCCGTAGT GGGCGTGGTGGTGCATGCCTGTAGTCCCAGCTCCTCAGGAGGCTGAGTCAGGAGAATCCCGTAGT A C LPP Ensembl:ENSG00000145012 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1340313428 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41507,RMVar_hsa_circ_119938,RMVar_hsa_circ_312627,RMVar_hsa_circ_369433,RMVar_hsa_circ_223622,RMVar_hsa_circ_363337,RMVar_hsa_circ_223623 2894 RMVar_ID_2894 Human_SNP_ID_167421501 A-to-I Human chr3 + 188260924 188260924 188260924 GGGCGTGGTGGTGCATGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGTCAGGAGAATCCCGTAGT GGGCGTGGTGGTGCATGCCTGTAGTCCCAGCTGCTCAGGAGGCTGAGTCAGGAGAATCCCGTAGT A G LPP Ensembl:ENSG00000145012 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1340313428 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41507,RMVar_hsa_circ_119938,RMVar_hsa_circ_312627,RMVar_hsa_circ_369433,RMVar_hsa_circ_223622,RMVar_hsa_circ_363337,RMVar_hsa_circ_223623 2895 RMVar_ID_2895 Human_SNP_ID_167425201 A-to-I Human chr3 + 188275873 188275873 188275873 AATTTTTTTGTTTTTAGTAGACATGGGGTTTCACCATATTGTCCAGGCTGATCTCGAACTCCTGA AATTTTTTTGTTTTTAGTAGACATGGGGTTTCGCCATATTGTCCAGGCTGATCTCGAACTCCTGA A G LPP Ensembl:ENSG00000145012 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1427551820 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14754251 RMVar_hsa_circ_41507,RMVar_hsa_circ_119938,RMVar_hsa_circ_312627,RMVar_hsa_circ_369433,RMVar_hsa_circ_223622,RMVar_hsa_circ_363337,RMVar_hsa_circ_223623 2896 RMVar_ID_2896 Human_SNP_ID_167510943 A-to-I Human chr3 + 188623357 188623357 188623357 TCAGCTCACTTCAACCTCCGCCTCCCAGGTTCAGGTGATTCTCCCGCCTCAGCCTCCAGAGTAGG TCAGCTCACTTCAACCTCCGCCTCCCAGGTTCGGGTGATTCTCCCGCCTCAGCCTCCAGAGTAGG A G LPP Ensembl:ENSG00000145012 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1255319017 Functional Loss SNV dbSNP153 33..33 33 - - - 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_344020,RMVar_hsa_circ_223632,RMVar_hsa_circ_71006,RMVar_hsa_circ_55780,RMVar_hsa_circ_364750,RMVar_hsa_circ_338803,RMVar_hsa_circ_352269,RMVar_hsa_circ_301000,RMVar_hsa_circ_223640,RMVar_hsa_circ_285376,RMVar_hsa_circ_223639 2897 RMVar_ID_2897 Human_SNP_ID_167552980 A-to-I Human chr3 + 188793382 188793382 188793382 TTTTGTATTTTTAGCAGAGATGGCGTTTTGTCATGTTGGAGAGACTGGTCTTGAACTCCTGACCT TTTTGTATTTTTAGCAGAGATGGCGTTTTGTCGTGTTGGAGAGACTGGTCTTGAACTCCTGACCT A G LPP Ensembl:ENSG00000145012 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs972394008 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105937,RMVar_hsa_circ_223628 2898 RMVar_ID_2898 Human_SNP_ID_167573269 A-to-I Human chr3 + 188877716 188877716 188877716 AAAAATAAAATAAAATAAAAACCAAATTAGCCAGACATGGTGGCATGCGCTTGTTTAAAAAAACA AAAAATAAAATAAAATAAAAACCAAATTAGCCGGACATGGTGGCATGCGCTTGTTTAAAAAAACA A G LPP Ensembl:ENSG00000145012 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1314341622 Functional Loss SNV dbSNP153 33..33 33 - - - 2899 RMVar_ID_2899 Human_SNP_ID_167573589 A-to-I Human chr3 + 188879039 188879039 188879039 TTTTTTAATTGTCTTCATTGTATTTGCTTAATAGTGGTCCAGACAAGTTCAAAACTTGTTCTCAG TTTTTTAATTGTCTTCATTGTATTTGCTTAATTGTGGTCCAGACAAGTTCAAAACTTGTTCTCAG A T LPP Ensembl:ENSG00000145012 Protein coding 3'UTR GSE100210;GSE99789 HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 29129909,29796672 RNA-Seq:(High) rs1436309240 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_597252 2900 RMVar_ID_2900 Human_SNP_ID_167574065 A-to-I Human chr3 + 188880897 188880897 188880897 CCAAATAAAATAGAATCATGCTTTGGGAGGCCAAGGCGGGCCGATCACGAGGTCAGGAGATCGAG CCAAATAAAATAGAATCATGCTTTGGGAGGCCGAGGCGGGCCGATCACGAGGTCAGGAGATCGAG A G LPP Ensembl:ENSG00000145012 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285586475 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2217124 2901 RMVar_ID_2901 Human_SNP_ID_167574117 A-to-I Human chr3 + 188880993 188880993 188880993 TCTACTAAAAAAAAAAAAAAATACAAAAAATTAGCCTGGCTCAGTGGCGGGCGCCTGTAGTCCCA TCTACTAAAAAAAAAAAAAAATACAAAAAATTGGCCTGGCTCAGTGGCGGGCGCCTGTAGTCCCA A G LPP Ensembl:ENSG00000145012 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1360803829 Functional Loss SNV dbSNP153 33..33 33 - - - 2902 RMVar_ID_2902 Human_SNP_ID_167574643 A-to-I Human chr3 + 188882880 188882880 188882880 CCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGACGCCCGCCACCGCGCCCAGCTAATTTTTTT CCTGCCTCAGCCTCCCGAGTAGCTGGGACTACGGACGCCCGCCACCGCGCCCAGCTAATTTTTTT A G LPP Ensembl:ENSG00000145012 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1035766441 Functional Loss SNV dbSNP153 33..33 33 - - - 2903 RMVar_ID_2903 Human_SNP_ID_167574655 A-to-I Human chr3 + 188882904 188882904 188882904 GGGACTACAGACGCCCGCCACCGCGCCCAGCTAATTTTTTTTGTACTTTTAGTAGAGACGGGGTT GGGACTACAGACGCCCGCCACCGCGCCCAGCTGATTTTTTTTGTACTTTTAGTAGAGACGGGGTT A G LPP Ensembl:ENSG00000145012 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs188692532 Functional Loss SNV dbSNP153 33..33 33 - - - 2904 RMVar_ID_2904 Human_SNP_ID_167574854 A-to-I Human chr3 + 188883622 188883622 188883622 GGGCGTGTTGGCGGGCGCCTGTAGTCCCAACTACTTGGGAGGCTGAGGCAGGAGAATCACCTGAA GGGCGTGTTGGCGGGCGCCTGTAGTCCCAACTGCTTGGGAGGCTGAGGCAGGAGAATCACCTGAA A G LPP Ensembl:ENSG00000145012 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1452189737 Functional Loss SNV dbSNP153 33..33 33 - - - 2905 RMVar_ID_2905 Human_SNP_ID_167865102 A-to-I Human chr3 - 190080584 190080584 190080584 TAGCCTGACCAACATGGAAAAACCCTGTCTTTACTAAAAATACAAAAAATTAACTGGGCGTGGTG TAGCCTGACCAACATGGAAAAACCCTGTCTTTGCTAAAAATACAAAAAATTAACTGGGCGTGGTG T C P3H2 Ensembl:ENSG00000090530 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1231774265 Functional Loss SNV dbSNP153 33..33 33 - - - 2906 RMVar_ID_2906 Human_SNP_ID_167865128 A-to-I Human chr3 - 190080681 190080681 190080681 TGCTCAAATCTCAGCTGGGCGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGC TGCTCAAATCTCAGCTGGGCGCGGTGGCTCACTCCTGTAATCCCAGCACTTTGGGAGGCCGAGGC T A P3H2 Ensembl:ENSG00000090530 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1286894486 Functional Loss SNV dbSNP153 33..33 33 - - - 2907 RMVar_ID_2907 Human_SNP_ID_168465673 A-to-I Human chr3 - 192538007 192538007 192538007 GGGAGTAGGAGGTTGCAGTGAGCCGAGATCGCACCATTGCACTCCAGCCTGGGGAGCAAGAGTGA GGGAGTAGGAGGTTGCAGTGAGCCGAGATCGCGCCATTGCACTCCAGCCTGGGGAGCAAGAGTGA T C FGF12 Ensembl:ENSG00000114279 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1331165546 Functional Loss SNV dbSNP153 33..33 33 - - - 2908 RMVar_ID_2908 Human_SNP_ID_168503166 A-to-I Human chr3 - 192695012 192695012 192695012 AGTTATCTTTTTTTTTGTTAAGAACACCTAAAATCTACTCCCCTAGCAAATTTTTAGTATATGTA AGTTATCTTTTTTTTTGTTAAGAACACCTAAATTCTACTCCCCTAGCAAATTTTTAGTATATGTA T A FGF12 Ensembl:ENSG00000114279 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444214535 Functional Loss SNV dbSNP153 33..33 33 - - - 2909 RMVar_ID_2909 Human_SNP_ID_168505524 A-to-I Human chr3 - 192706021 192706021 192706021 TAAGGATTAACAGATGAAATTCTGTATGAGAAACCAATTGTGTCTACAGCACCTAAAGCACATTC TAAGGATTAACAGATGAAATTCTGTATGAGAACCCAATTGTGTCTACAGCACCTAAAGCACATTC T G FGF12 Ensembl:ENSG00000114279 Protein coding intron GSE107867 ASD brains,cerebellum;ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1156987873 Functional Loss SNV dbSNP153 33..33 33 - - - 2910 RMVar_ID_2910 Human_SNP_ID_168539846 A-to-I Human chr3 - 192845844 192845844 192845844 GAACTCCTGGCCTCAAGCAATCCCCCTACCTCAGTCTCCCAAAGTGCAGGGACTATAGGCATGAG GAACTCCTGGCCTCAAGCAATCCCCCTACCTCCGTCTCCCAAAGTGCAGGGACTATAGGCATGAG T G MB21D2 Ensembl:ENSG00000180611 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1181759255 Functional Loss SNV dbSNP153 33..33 33 - - - 2911 RMVar_ID_2911 Human_SNP_ID_168722661 A-to-I Human chr3 + 193596936 193596936 193596936 AAAGAAGACGTGTGAGACTCCGTACTGAAACTAAAGACGACTTGTGAGTTCCACACTGAGATCAA AAAGAAGACGTGTGAGACTCCGTACTGAAACTGAAGACGACTTGTGAGTTCCACACTGAGATCAA A G OPA1 Ensembl:ENSG00000198836 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1317700019 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_524945 2912 RMVar_ID_2912 Human_SNP_ID_168731384 A-to-I Human chr3 + 193632771 193632771 193632771 GTTGTGCCTGTAGTCCCAGCAACTGGGAGGCTAAGGCGGGAGGATCACTTGAGCCCCAGGAGGTC GTTGTGCCTGTAGTCCCAGCAACTGGGAGGCTGAGGCGGGAGGATCACTTGAGCCCCAGGAGGTC A G OPA1 Ensembl:ENSG00000198836 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170174624 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4867,RMVar_hsa_circ_5831,RMVar_hsa_circ_19551,RMVar_hsa_circ_63119,RMVar_hsa_circ_350577,RMVar_hsa_circ_269822,RMVar_hsa_circ_122247,RMVar_hsa_circ_370602,RMVar_hsa_circ_376901,RMVar_hsa_circ_355054,RMVar_hsa_circ_52500,RMVar_hsa_circ_66986,RMVar_hsa_circ_33386,RMVar_hsa_circ_61700,RMVar_hsa_circ_330133,RMVar_hsa_circ_223701,RMVar_hsa_circ_223702,RMVar_hsa_circ_223700,RMVar_hsa_circ_360171,RMVar_hsa_circ_323936,RMVar_hsa_circ_50532,RMVar_hsa_circ_21201,RMVar_hsa_circ_63160,RMVar_hsa_circ_32360,RMVar_hsa_circ_377226,RMVar_hsa_circ_358095,RMVar_hsa_circ_362905,RMVar_hsa_circ_73397,RMVar_hsa_circ_24379,RMVar_hsa_circ_31840,RMVar_hsa_circ_14495,RMVar_hsa_circ_57816 2913 RMVar_ID_2913 Human_SNP_ID_168899456 A-to-I Human chr3 - 194298139 194298139 194298139 CCAGACTGTGCTTGAACTCCTGGCCTCAAGCAATCCTCCCACTTCAGCCCCAAGAGTTGCTGGGA CCAGACTGTGCTTGAACTCCTGGCCTCAAGCAGTCCTCCCACTTCAGCCCCAAGAGTTGCTGGGA T C LINC00887 Ensembl:ENSG00000214145 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1258828637 Functional Loss SNV dbSNP153 33..33 33 - - - 2914 RMVar_ID_2914 Human_SNP_ID_168899486 A-to-I Human chr3 - 194298278 194298278 194298278 ACAGCTCCCTGGAGGCTTAAACTCCTGGGCTCAAGCAATTCTCGTGTCTCAGCCCCCTGAGTCGC ACAGCTCCCTGGAGGCTTAAACTCCTGGGCTCGAGCAATTCTCGTGTCTCAGCCCCCTGAGTCGC T C LINC00887 Ensembl:ENSG00000214145 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215736254 Functional Loss SNV dbSNP153 33..33 33 - - - 2915 RMVar_ID_2915 Human_SNP_ID_168930237 A-to-I Human chr3 - 194406292 194406292 194406292 CCAAGATGCTGGGATTTCGGACATGAGCCACCACGCCCGGCCAAAGCTGCCTTTTTTTAACATGG CCAAGATGCTGGGATTTCGGACATGAGCCACCGCGCCCGGCCAAAGCTGCCTTTTTTTAACATGG T C ATP13A3 Ensembl:ENSG00000133657 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs567934403 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8568361 2916 RMVar_ID_2916 Human_SNP_ID_168976899 A-to-I Human chr3 + 194585390 194585390 194585390 AGTTCCAGATCAGGCTGGCCAACAGCGTCTCTACTAAAAATACAAAAATTAGCCAGGCATGGTGG AGTTCCAGATCAGGCTGGCCAACAGCGTCTCTGCTAAAAATACAAAAATTAGCCAGGCATGGTGG A G TMEM44-AS1 Ensembl:ENSG00000231770 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs943984221 Functional Loss SNV dbSNP153 33..33 33 - - - 2917 RMVar_ID_2917 Human_SNP_ID_168977922 A-to-I Human chr3 + 194589234 194589234 194589234 GTTGCCCAGGCTGATCTCGAACTCCTGGACCTAAGCAGTCCTCCCGCCTCAGCCTCCCAAAGTGC GTTGCCCAGGCTGATCTCGAACTCCTGGACCTCAGCAGTCCTCCCGCCTCAGCCTCCCAAAGTGC A C TMEM44-AS1 Ensembl:ENSG00000231770 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs12490914 Functional Loss SNV dbSNP153 33..33 33 - - - 2918 RMVar_ID_2918 Human_SNP_ID_168981219 A-to-I Human chr3 - 194600554 194600554 194600554 TTAGTAGAGATGAGGTTTCACCATGTTGGCCAAGATGGTCACGATCTCCTGACCTCGTGACCTGC TTAGTAGAGATGAGGTTTCACCATGTTGGCCACGATGGTCACGATCTCCTGACCTCGTGACCTGC T G TMEM44 Ensembl:ENSG00000145014 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048052697 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21095,RMVar_hsa_circ_100341,RMVar_hsa_circ_223750 2919 RMVar_ID_2919 Human_SNP_ID_168984978 A-to-I Human chr3 - 194614542 194614542 194614542 AAAATTGGCCGGGTATGGTGGTGTGTGCCTGTAGTCCCAGCTACTTAGGAGGCTGAGGCAGGAGG AAAATTGGCCGGGTATGGTGGTGTGTGCCTGTGGTCCCAGCTACTTAGGAGGCTGAGGCAGGAGG T C TMEM44 Ensembl:ENSG00000145014 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1478811338 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_684,RMVar_hsa_circ_100341,RMVar_hsa_circ_332127,RMVar_hsa_circ_223750,RMVar_hsa_circ_347265,RMVar_hsa_circ_299583,RMVar_hsa_circ_46959,RMVar_hsa_circ_31894,RMVar_hsa_circ_95243,RMVar_hsa_circ_223752,RMVar_hsa_circ_316735,RMVar_hsa_circ_52378,RMVar_hsa_circ_21875,RMVar_hsa_circ_22435,RMVar_hsa_circ_223753 2920 RMVar_ID_2920 Human_SNP_ID_168985579 A-to-I Human chr3 - 194616812 194616812 194616812 TGGCTCACTGCAACCTTCACCTCCCAATTTCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCT TGGCTCACTGCAACCTTCACCTCCCAATTTCAGGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCT T C TMEM44 Ensembl:ENSG00000145014 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1030309416 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_155169 Human_Splice_Rec_526938,Human_Splice_Rec_526939 RMVar_hsa_circ_684,RMVar_hsa_circ_100341,RMVar_hsa_circ_223750,RMVar_hsa_circ_347265,RMVar_hsa_circ_46959,RMVar_hsa_circ_31894,RMVar_hsa_circ_95243,RMVar_hsa_circ_316735,RMVar_hsa_circ_52378,RMVar_hsa_circ_115997,RMVar_hsa_circ_223753,RMVar_hsa_circ_223754 2921 RMVar_ID_2921 Human_SNP_ID_168987007 A-to-I Human chr3 - 194621759 194621759 194621759 TGAGCCGAGATCGTGCTGCTGCACTCCATCCTAGGTGACTGAGCACTACTCCATCTAAAAAAAAA TGAGCCGAGATCGTGCTGCTGCACTCCATCCTCGGTGACTGAGCACTACTCCATCTAAAAAAAAA T G TMEM44 Ensembl:ENSG00000145014 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs1319316971 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_684,RMVar_hsa_circ_46959,RMVar_hsa_circ_31894,RMVar_hsa_circ_52378 2922 RMVar_ID_2922 Human_SNP_ID_168987027 A-to-I Human chr3 - 194621819 194621819 194621819 TAATCCCAGCTACTGTGGAGGCAGGATGGATCACTTGAATCCAGGAGGTGGGGGTTGCAGTGAGC TAATCCCAGCTACTGTGGAGGCAGGATGGATCGCTTGAATCCAGGAGGTGGGGGTTGCAGTGAGC T C TMEM44 Ensembl:ENSG00000145014 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1160897261 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_684,RMVar_hsa_circ_46959,RMVar_hsa_circ_31894,RMVar_hsa_circ_52378 2923 RMVar_ID_2923 Human_SNP_ID_168987046 A-to-I Human chr3 - 194621885 194621884 194621886 CAACATGCTGAAACCCCGTCTCTACTAAAAATACAAAAACTAGCCAGGCGTGGTGGCGGGTGCCT CAACATGCTGAAACCCCGTCTCTACTAAAAA__CAAAAACTAGCCAGGCGTGGTGGCGGGTGCCT GTA G TMEM44 Ensembl:ENSG00000145014 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1384853925 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_684,RMVar_hsa_circ_46959,RMVar_hsa_circ_31894,RMVar_hsa_circ_52378 2924 RMVar_ID_2924 Human_SNP_ID_168987299 A-to-I Human chr3 - 194622686 194622686 194622686 AAATTAGCCAGGCATGGTGGTGCATGCTTGTAATCCCAGCTACTCTGGAGGCTGAGGTGGAGAAT AAATTAGCCAGGCATGGTGGTGCATGCTTGTAGTCCCAGCTACTCTGGAGGCTGAGGTGGAGAAT T C TMEM44 Ensembl:ENSG00000145014 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1464079773 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_684,RMVar_hsa_circ_46959,RMVar_hsa_circ_31894,RMVar_hsa_circ_52378 2925 RMVar_ID_2925 Human_SNP_ID_168990981 A-to-I Human chr3 - 194634353 194634353 194634353 AATACAAAAATTACTCGGGTGTGGTGGCGGGCACCTGTAGTCCCAGCTACTTGGGAGGCGGAGGC AATACAAAAATTACTCGGGTGTGGTGGCGGGCTCCTGTAGTCCCAGCTACTTGGGAGGCGGAGGC T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1009959918 Functional Loss SNV dbSNP153 33..33 33 - - - 2926 RMVar_ID_2926 Human_SNP_ID_168990982 A-to-I Human chr3 - 194634353 194634353 194634353 AATACAAAAATTACTCGGGTGTGGTGGCGGGCACCTGTAGTCCCAGCTACTTGGGAGGCGGAGGC AATACAAAAATTACTCGGGTGTGGTGGCGGGCGCCTGTAGTCCCAGCTACTTGGGAGGCGGAGGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1009959918 Functional Loss SNV dbSNP153 33..33 33 - - - 2927 RMVar_ID_2927 Human_SNP_ID_168991542 A-to-I Human chr3 + 194636607 194636607 194636607 GCCTGTAATCCCAGCAATTCGGGGGGTGAGGCAAGTGGATCACTTGAGCTCTGGAGTTCGAGGTC GCCTGTAATCCCAGCAATTCGGGGGGTGAGGCGAGTGGATCACTTGAGCTCTGGAGTTCGAGGTC A G AC046143.1 Ensembl:ENSG00000229334 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6788774 Functional Loss SNV dbSNP153 33..33 33 - - - 2928 RMVar_ID_2928 Human_SNP_ID_168991543 A-to-I Human chr3 + 194636607 194636607 194636607 GCCTGTAATCCCAGCAATTCGGGGGGTGAGGCAAGTGGATCACTTGAGCTCTGGAGTTCGAGGTC GCCTGTAATCCCAGCAATTCGGGGGGTGAGGCTAGTGGATCACTTGAGCTCTGGAGTTCGAGGTC A T AC046143.1 Ensembl:ENSG00000229334 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6788774 Functional Loss SNV dbSNP153 33..33 33 - - - 2929 RMVar_ID_2929 Human_SNP_ID_168995541 A-to-I Human chr3 - 194649504 194649499 194649504 TTTTTTTTTTTTTTTGGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTCTTGA TTTTTTTTTTTTTTTGGTAGAGATGGGGTTTC_____GTTGGCCAGGCTGGTCTCAAACTCTTGA CATGGT C LSG1 Ensembl:ENSG00000041802 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1458758637 Functional Loss DEL dbSNP153 33..37 33 - - - RMVar_hsa_circ_223756,RMVar_hsa_circ_94448,RMVar_hsa_circ_123723,RMVar_hsa_circ_113119,RMVar_hsa_circ_223758,RMVar_hsa_circ_84004,RMVar_hsa_circ_223757,RMVar_hsa_circ_223755 2930 RMVar_ID_2930 Human_SNP_ID_168995575 A-to-I Human chr3 - 194649603 194649603 194649603 TCACTGCAACCTCCACCTCCTGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGA TCACTGCAACCTCCACCTCCTGGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGA T C LSG1 Ensembl:ENSG00000041802 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs531230037 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_223756,RMVar_hsa_circ_94448,RMVar_hsa_circ_123723,RMVar_hsa_circ_113119,RMVar_hsa_circ_223758,RMVar_hsa_circ_84004,RMVar_hsa_circ_223757,RMVar_hsa_circ_223755 2931 RMVar_ID_2931 Human_SNP_ID_168995731 A-to-I Human chr3 - 194650186 194650186 194650186 GGCCAGGTGTGGTGGTTCATGCCTGTAACCCCAACACTTTGGGAGGCTGTGGCAGGCGGATCACT GGCCAGGTGTGGTGGTTCATGCCTGTAACCCCGACACTTTGGGAGGCTGTGGCAGGCGGATCACT T C LSG1 Ensembl:ENSG00000041802 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs886338071 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_223756,RMVar_hsa_circ_94448,RMVar_hsa_circ_123723,RMVar_hsa_circ_113119,RMVar_hsa_circ_223758,RMVar_hsa_circ_84004,RMVar_hsa_circ_223757,RMVar_hsa_circ_223755 2932 RMVar_ID_2932 Human_SNP_ID_168998268 A-to-I Human chr3 - 194660115 194660115 194660115 TGTTTGTTTTTCAGTGATATTGTGGTCCAGATAGTAGATGCTCGAAACCCACTCCTGTTTAGATG TGTTTGTTTTTCAGTGATATTGTGGTCCAGATGGTAGATGCTCGAAACCCACTCCTGTTTAGATG T C LSG1 Ensembl:ENSG00000041802 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1244061036 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14758726,Human_RBP_ID_18804906,Human_RBP_ID_23992156 Human_Splice_Rec_526992,Human_Splice_Rec_526993,Human_Splice_Rec_527042,Human_Splice_Rec_527043 RMVar_hsa_circ_223756,RMVar_hsa_circ_94448,RMVar_hsa_circ_123723,RMVar_hsa_circ_54090,RMVar_hsa_circ_223755,RMVar_hsa_circ_269769,RMVar_hsa_circ_44418,RMVar_hsa_circ_223761 2933 RMVar_ID_2933 Human_SNP_ID_169005648 A-to-I Human chr3 + 194688792 194688792 194688792 ACACACACCCTTCCTCTTGCTCAAAAGATCTCACTCCATGATACTGTGTAAAATATTTTTGCACT ACACACACCCTTCCTCTTGCTCAAAAGATCTCGCTCCATGATACTGTGTAAAATATTTTTGCACT A G FAM43A Ensembl:ENSG00000185112 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs572600654 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_96554 2934 RMVar_ID_2934 Human_SNP_ID_178541917 A-to-I Human chr4 + 30736615 30736615 30736615 TGGAGTGTAGTTCCGCGATCTCGGCTCACTGCAAGCTCCGCCTCCCGGATTCGCGCCATTCTCCT TGGAGTGTAGTTCCGCGATCTCGGCTCACTGCCAGCTCCGCCTCCCGGATTCGCGCCATTCTCCT A C PCDH7 Ensembl:ENSG00000169851 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs142584822 Functional Loss SNV dbSNP153 33..33 33 - - - 2935 RMVar_ID_2935 Human_SNP_ID_178541918 A-to-I Human chr4 + 30736615 30736615 30736615 TGGAGTGTAGTTCCGCGATCTCGGCTCACTGCAAGCTCCGCCTCCCGGATTCGCGCCATTCTCCT TGGAGTGTAGTTCCGCGATCTCGGCTCACTGCTAGCTCCGCCTCCCGGATTCGCGCCATTCTCCT A T PCDH7 Ensembl:ENSG00000169851 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs142584822 Functional Loss SNV dbSNP153 33..33 33 - - - 2936 RMVar_ID_2936 Human_SNP_ID_178549043 A-to-I Human chr4 + 30764833 30764833 30764833 ACCTCCCCCTCCCTGGTTCAAGCTATTCTCCTACCTCAGCCTCCAGAGTAGCTTGGATTATAGGC ACCTCCCCCTCCCTGGTTCAAGCTATTCTCCTGCCTCAGCCTCCAGAGTAGCTTGGATTATAGGC A G PCDH7 Ensembl:ENSG00000169851 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs967043321 Functional Loss SNV dbSNP153 33..33 33 - - - 2937 RMVar_ID_2937 Human_SNP_ID_178558499 A-to-I Human chr4 + 30803700 30803700 30803700 ACTTAAAACCATCCTCCTGCCTTGGTGTCCCAAAGTGCTGGGATTACAGGCATAAGCCACTGTGC ACTTAAAACCATCCTCCTGCCTTGGTGTCCCAGAGTGCTGGGATTACAGGCATAAGCCACTGTGC A G PCDH7 Ensembl:ENSG00000169851 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910621168 Functional Loss SNV dbSNP153 33..33 33 - - - 2938 RMVar_ID_2938 Human_SNP_ID_178558500 A-to-I Human chr4 + 30803700 30803700 30803700 ACTTAAAACCATCCTCCTGCCTTGGTGTCCCAAAGTGCTGGGATTACAGGCATAAGCCACTGTGC ACTTAAAACCATCCTCCTGCCTTGGTGTCCCATAGTGCTGGGATTACAGGCATAAGCCACTGTGC A T PCDH7 Ensembl:ENSG00000169851 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910621168 Functional Loss SNV dbSNP153 33..33 33 - - - 2939 RMVar_ID_2939 Human_SNP_ID_178558503 A-to-I Human chr4 + 30803713 30803713 30803713 CTCCTGCCTTGGTGTCCCAAAGTGCTGGGATTACAGGCATAAGCCACTGTGCATAGCACATGCAA CTCCTGCCTTGGTGTCCCAAAGTGCTGGGATTGCAGGCATAAGCCACTGTGCATAGCACATGCAA A G PCDH7 Ensembl:ENSG00000169851 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1425144864 Functional Loss SNV dbSNP153 33..33 33 - - - 2940 RMVar_ID_2940 Human_SNP_ID_178598609 A-to-I Human chr4 + 30962661 30962661 30962661 ATTAAAAATAGCAAGGTATGGTGGTGCTCTGTAGTGGCAGCTATTCTGGAGGCTGAGGCAGGAAG ATTAAAAATAGCAAGGTATGGTGGTGCTCTGTGGTGGCAGCTATTCTGGAGGCTGAGGCAGGAAG A G PCDH7 Ensembl:ENSG00000169851 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs899800263 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76075,RMVar_hsa_circ_225284 2941 RMVar_ID_2941 Human_SNP_ID_180397969 A-to-I Human chr4 + 37864618 37864618 37864618 GTTTGGGTTTTTGGTAGAGGCAGGGTTTTACCATGTTGCCCAGACTGGTCTCGAACTCTTGACCT GTTTGGGTTTTTGGTAGAGGCAGGGTTTTACCGTGTTGCCCAGACTGGTCTCGAACTCTTGACCT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1371349742 Functional Loss SNV dbSNP153 33..33 33 - - - 2942 RMVar_ID_2942 Human_SNP_ID_180398014 A-to-I Human chr4 + 37864794 37864794 37864794 CTTTGTACGAAAGAAGGCAGGCTTGTGTTCCTATCTTGCTTTGCCTTGAAGCCTGAAGGGGATGA CTTTGTACGAAAGAAGGCAGGCTTGTGTTCCTGTCTTGCTTTGCCTTGAAGCCTGAAGGGGATGA A G - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1237750558 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25808723 2943 RMVar_ID_2943 Human_SNP_ID_180399098 A-to-I Human chr4 + 37869481 37869481 37869481 CCAGCTCACCACAACCTCCGCCTCCTGGGTTCAAGCAATTCTCCTGCCTTAGCTGGGATTACAGG CCAGCTCACCACAACCTCCGCCTCCTGGGTTCGAGCAATTCTCCTGCCTTAGCTGGGATTACAGG A G AC021106.1 Ensembl:ENSG00000249863 Pseudogene intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1448587382 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17409974 2944 RMVar_ID_2944 Human_SNP_ID_180399706 A-to-I Human chr4 + 37872006 37872006 37872006 AAAGAACAACAAAAAAAGAAGGAAATCCTGCCATTTGTGACAACATGGATGAACCTGGAGGACAT AAAGAACAACAAAAAAAGAAGGAAATCCTGCCGTTTGTGACAACATGGATGAACCTGGAGGACAT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1396831218 Functional Loss SNV dbSNP153 33..33 33 - - - 2945 RMVar_ID_2945 Human_SNP_ID_180399761 A-to-I Human chr4 + 37872253 37872253 37872253 GTTCTGGGGGTCTAATGTAGCACATGGCAACTATGGTTAACAATACTGTATTGTATACTTGAAAT GTTCTGGGGGTCTAATGTAGCACATGGCAACTGTGGTTAACAATACTGTATTGTATACTTGAAAT A G - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1011461612 Functional Loss SNV dbSNP153 33..33 33 - - - 2946 RMVar_ID_2946 Human_SNP_ID_180582028 A-to-I Human chr4 - 38644365 38644364 38644365 CCCCTGTCTCAGCCTCTCGAGTAGCTGGGACTACAGGCATGCGCCACCACACCCAGTTTGAACAC CCCCTGTCTCAGCCTCTCGAGTAGCTGGGACT_CAGGCATGCGCCACCACACCCAGTTTGAACAC GT G KLF3-AS1 Ensembl:ENSG00000231160 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270046133 Functional Loss DEL dbSNP153 33..33 33 - - - 2947 RMVar_ID_2947 Human_SNP_ID_180590215 A-to-I Human chr4 + 38677035 38677035 38677035 CCAAGCTGAGTGCAGTGGTGCTATTTGGGCTCACTGCAACCTCCGCCTGCTGGGTTCAAGCGATT CCAAGCTGAGTGCAGTGGTGCTATTTGGGCTCGCTGCAACCTCCGCCTGCTGGGTTCAAGCGATT A G KLF3 Ensembl:ENSG00000109787 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1396770050 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78058,RMVar_hsa_circ_225372 2948 RMVar_ID_2948 Human_SNP_ID_180616963 A-to-I Human chr4 - 38780314 38780314 38780314 CTGCAACCTCCACCTTTTGGGTTCAAGTGATTATCCTGCCTCAGCCTCCCGAGTAGCTGGGACTA CTGCAACCTCCACCTTTTGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTA T G TLR10 Ensembl:ENSG00000174123 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1301403079 Functional Loss SNV dbSNP153 33..33 33 - - - 2949 RMVar_ID_2949 Human_SNP_ID_180645020 A-to-I Human chr4 + 38894587 38894587 38894587 GAGCACAGTCCACTGGAACCAAATCTGCACGTATGCAAAGATCAGATTACAAAAGGACACCTAAG GAGCACAGTCCACTGGAACCAAATCTGCACGTGTGCAAAGATCAGATTACAAAAGGACACCTAAG A G FAM114A1 Ensembl:ENSG00000197712 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991988066 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72043,RMVar_hsa_circ_346062,RMVar_hsa_circ_356777,RMVar_hsa_circ_361186,RMVar_hsa_circ_349429,RMVar_hsa_circ_65201,RMVar_hsa_circ_352782,RMVar_hsa_circ_354285,RMVar_hsa_circ_69362,RMVar_hsa_circ_35310 2950 RMVar_ID_2950 Human_SNP_ID_180645475 A-to-I Human chr4 + 38896668 38896668 38896668 CCTTCCTGATCTGTGGTCTATGTTGAGCCACTATCTTGGGATTGAGAGAGGCAAGCGAGGCACAA CCTTCCTGATCTGTGGTCTATGTTGAGCCACTCTCTTGGGATTGAGAGAGGCAAGCGAGGCACAA A C FAM114A1 Ensembl:ENSG00000197712 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1284411370 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72043,RMVar_hsa_circ_346062,RMVar_hsa_circ_356777,RMVar_hsa_circ_361186,RMVar_hsa_circ_349429,RMVar_hsa_circ_65201,RMVar_hsa_circ_352782,RMVar_hsa_circ_354285,RMVar_hsa_circ_69362,RMVar_hsa_circ_35310 2951 RMVar_ID_2951 Human_SNP_ID_180649726 A-to-I Human chr4 + 38914406 38914406 38914406 GGGCAACATGGTGAAACCCTGTCTCTACCAAAAAATACAAAAATTAGCTGGGCATGGTGGCAAGG GGGCAACATGGTGAAACCCTGTCTCTACCAAACAATACAAAAATTAGCTGGGCATGGTGGCAAGG A C FAM114A1 Ensembl:ENSG00000197712 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs566871465 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4204,RMVar_hsa_circ_72043,RMVar_hsa_circ_346062,RMVar_hsa_circ_356777,RMVar_hsa_circ_361186,RMVar_hsa_circ_352782,RMVar_hsa_circ_354285,RMVar_hsa_circ_69362,RMVar_hsa_circ_319019,RMVar_hsa_circ_357818,RMVar_hsa_circ_351726 2952 RMVar_ID_2952 Human_SNP_ID_180657226 A-to-I Human chr4 + 38944674 38944673 38944675 GCTCTGCCTCCCGTCAGGTCAGCAGCAGCATTAGAGTCTCATGGGAGTGCGAACCCTGTTGTGAA GCTCTGCCTCCCGTCAGGTCAGCAGCAGCATT__AGTCTCATGGGAGTGCGAACCCTGTTGTGAA TAG T FAM114A1 Ensembl:ENSG00000197712 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1396944106 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_8212344,Human_RBP_ID_26518067 RMVar_hsa_circ_125537,RMVar_hsa_circ_225384 2953 RMVar_ID_2953 Human_SNP_ID_180679546 A-to-I Human chr4 - 39032660 39032660 39032660 TGCTGGGATTACAGATGTGAGCCACTTCGCCCAGCCCACCGTTTTATTTTTGTGAGTATACTGTG TGCTGGGATTACAGATGTGAGCCACTTCGCCCCGCCCACCGTTTTATTTTTGTGAGTATACTGTG T G TMEM156 Ensembl:ENSG00000121895 Protein coding 5'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs933842513 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_554119,Human_Splice_Rec_554129 2954 RMVar_ID_2954 Human_SNP_ID_180679562 A-to-I Human chr4 - 39032754 39032754 39032754 AAATTATTTTTGTAGAGAGGAGGGCTTGCTCTATTGACCAGTCTGGACTCAAACTCCTGAACTCA AAATTATTTTTGTAGAGAGGAGGGCTTGCTCTCTTGACCAGTCTGGACTCAAACTCCTGAACTCA T G TMEM156 Ensembl:ENSG00000121895 Protein coding 5'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1416080315 Functional Loss SNV dbSNP153 33..33 33 - - - 2955 RMVar_ID_2955 Human_SNP_ID_180679579 A-to-I Human chr4 - 39032818 39032818 39032818 AGTGATCCTCAGCTTCCTGAGTAGCTGGGACTACAGGAGTGCACCACCACACCTAGCTATATTAA AGTGATCCTCAGCTTCCTGAGTAGCTGGGACTGCAGGAGTGCACCACCACACCTAGCTATATTAA T C TMEM156 Ensembl:ENSG00000121895 Protein coding 5'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs1318236377 Functional Loss SNV dbSNP153 33..33 33 - - - 2956 RMVar_ID_2956 Human_SNP_ID_180682997 A-to-I Human chr4 + 39047320 39047316 39047320 CGTACCTGTAGTCCCAGCTACTAAGGAGGCTGAAGGAGGAGAATCGCTTGAACCTGAGAGGTGGA CGTACCTGTAGTCCCAGCTACTAAGGAGG____AGGAGGAGAATCGCTTGAACCTGAGAGGTGGA GCTGA G KLHL5 Ensembl:ENSG00000109790 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1346954156 Functional Loss DEL dbSNP153 30..33 33 - - - 2957 RMVar_ID_2957 Human_SNP_ID_180682999 A-to-I Human chr4 + 39047320 39047320 39047320 CGTACCTGTAGTCCCAGCTACTAAGGAGGCTGAAGGAGGAGAATCGCTTGAACCTGAGAGGTGGA CGTACCTGTAGTCCCAGCTACTAAGGAGGCTGCAGGAGGAGAATCGCTTGAACCTGAGAGGTGGA A C KLHL5 Ensembl:ENSG00000109790 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1015262325 Functional Loss SNV dbSNP153 33..33 33 - - - 2958 RMVar_ID_2958 Human_SNP_ID_180698479 A-to-I Human chr4 + 39117254 39117254 39117254 CCCAGGAGTTGAGGCTGAAGTGAACCATGATCATGACACTGCACTCCAGCCTGGACAACAGAGCA CCCAGGAGTTGAGGCTGAAGTGAACCATGATCTTGACACTGCACTCCAGCCTGGACAACAGAGCA A T KLHL5 Ensembl:ENSG00000109790 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1332328026 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268789,RMVar_hsa_circ_121971,RMVar_hsa_circ_225396 2959 RMVar_ID_2959 Human_SNP_ID_180734391 A-to-I Human chr4 + 39280164 39280164 39280164 TTTTTTTTTTAATAGAGGCAGGGTCTCGCCACATTGCGCAGATTGGTCTCGAACTCCTAGGCTCA TTTTTTTTTTAATAGAGGCAGGGTCTCGCCACGTTGCGCAGATTGGTCTCGAACTCCTAGGCTCA A G WDR19 Ensembl:ENSG00000157796 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1265225762 Functional Loss SNV dbSNP153 33..33 33 - - - 2960 RMVar_ID_2960 Human_SNP_ID_180736593 A-to-I Human chr4 - 39287839 39287838 39287839 AGGCTCTTAATTTCACTATGGTGGGGGACAAAATGAACACTGGCTTTTGTTCACTTTGCCCCTGA AGGCTCTTAATTTCACTATGGTGGGGGACAAA_TGAACACTGGCTTTTGTTCACTTTGCCCCTGA AT A RFC1 Ensembl:ENSG00000035928 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1480081673 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_620103,Human_RBP_ID_8211946,Human_RBP_ID_18025872,Human_RBP_ID_18823874,Human_RBP_ID_24054417,Human_RBP_ID_26518359 Human_miRNA_ID_1787746,Human_miRNA_ID_2174618,Human_miRNA_ID_2178061 RMVar_hsa_circ_87174,RMVar_hsa_circ_225414 2961 RMVar_ID_2961 Human_SNP_ID_180741103 A-to-I Human chr4 - 39305491 39305491 39305491 TGATTCTCATGCCTCACCCTCCAGAGTAGCTGAGACTACAGGAACACGCCACCACGCCCAGCTAA TGATTCTCATGCCTCACCCTCCAGAGTAGCTGGGACTACAGGAACACGCCACCACGCCCAGCTAA T C RFC1 Ensembl:ENSG00000035928 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1560595136 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15145265 RMVar_hsa_circ_24225,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_56322,RMVar_hsa_circ_72296,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_56377,RMVar_hsa_circ_59502,RMVar_hsa_circ_13800,RMVar_hsa_circ_225424,RMVar_hsa_circ_308041,RMVar_hsa_circ_329210,RMVar_hsa_circ_342185,RMVar_hsa_circ_362226,RMVar_hsa_circ_338414,RMVar_hsa_circ_317600,RMVar_hsa_circ_69953,RMVar_hsa_circ_225422,RMVar_hsa_circ_225423,RMVar_hsa_circ_225421 2962 RMVar_ID_2962 Human_SNP_ID_180745733 A-to-I Human chr4 - 39325571 39325571 39325571 TGAGACCAGTCTGGGTAACATAGGGAAATCCCATCTCTACCAAAAATACAAAAATCAACTGGGCA TGAGACCAGTCTGGGTAACATAGGGAAATCCCTTCTCTACCAAAAATACAAAAATCAACTGGGCA T A RFC1 Ensembl:ENSG00000035928 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1343918970 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104833,RMVar_hsa_circ_225420,RMVar_hsa_circ_57704,RMVar_hsa_circ_37552,RMVar_hsa_circ_225424,RMVar_hsa_circ_342185,RMVar_hsa_circ_324193,RMVar_hsa_circ_344841,RMVar_hsa_circ_56425,RMVar_hsa_circ_349953 2963 RMVar_ID_2963 Human_SNP_ID_180746168 A-to-I Human chr4 - 39327650 39327650 39327650 CTTGGAACATCAAACATGAAAAAGAATGAAGAAAACACTAAGACCAAGAATAAGCCTTTATCACC CTTGGAACATCAAACATGAAAAAGAATGAAGAGAACACTAAGACCAAGAATAAGCCTTTATCACC T C RFC1 Ensembl:ENSG00000035928 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs773664928 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9396273,Human_RBP_ID_18413530,Human_RBP_ID_21082155,Human_RBP_ID_26349248,Human_RBP_ID_27824043 RMVar_hsa_circ_104833,RMVar_hsa_circ_225420,RMVar_hsa_circ_57704,RMVar_hsa_circ_37552,RMVar_hsa_circ_225424,RMVar_hsa_circ_342185,RMVar_hsa_circ_324193,RMVar_hsa_circ_344841,RMVar_hsa_circ_56425,RMVar_hsa_circ_349953,RMVar_hsa_circ_65154,RMVar_hsa_circ_288775,RMVar_hsa_circ_225428 2964 RMVar_ID_2964 Human_SNP_ID_180794621 A-to-I Human chr4 - 39523622 39523622 39523622 TTTTGTATTTTTAGTAGAGATGGGGTTTTGTCATGTTGATCAGGCTGGTCTTGAACTCCTGACCT TTTTGTATTTTTAGTAGAGATGGGGTTTTGTCTTGTTGATCAGGCTGGTCTTGAACTCCTGACCT T A UGDH Ensembl:ENSG00000109814 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1266726938 Functional Loss SNV dbSNP153 33..33 33 - - - 2965 RMVar_ID_2965 Human_SNP_ID_180796399 A-to-I Human chr4 + 39530918 39530918 39530918 GGGCCCGGCCCACAAAACCATTTTTTCTTCCTAAACCTCCAGGCCTGTGATGGGAGGAGCTGCCA GGGCCCGGCCCACAAAACCATTTTTTCTTCCTGAACCTCCAGGCCTGTGATGGGAGGAGCTGCCA A G UGDH-AS1 Ensembl:ENSG00000249348 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1358482444 Functional Loss SNV dbSNP153 33..33 33 - - - 2966 RMVar_ID_2966 Human_SNP_ID_180796859 A-to-I Human chr4 + 39532852 39532852 39532852 AACTGGAGCAAAGGTGACTCTTGTTATGTTTTAGCAAAGAGACTGGTGACATTTTGCCCCTGCCC AACTGGAGCAAAGGTGACTCTTGTTATGTTTTGGCAAAGAGACTGGTGACATTTTGCCCCTGCCC A G UGDH-AS1 Ensembl:ENSG00000249348 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs571893219 Functional Loss SNV dbSNP153 33..33 33 - - - 2967 RMVar_ID_2967 Human_SNP_ID_180796908 A-to-I Human chr4 + 39533041 39533041 39533041 CTCAGCTTACTGGGTTCAAGCAATTCTGTCTCAGCCTCCCGAGTAGCTGGGATTACAGGCGTCCG CTCAGCTTACTGGGTTCAAGCAATTCTGTCTCGGCCTCCCGAGTAGCTGGGATTACAGGCGTCCG A G UGDH-AS1 Ensembl:ENSG00000249348 lincRNA intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs888207612 Functional Loss SNV dbSNP153 33..33 33 - - - 2968 RMVar_ID_2968 Human_SNP_ID_180796933 A-to-I Human chr4 + 39533108 39533108 39533108 ACCACGCCCTTCTAATTTTTTGTATTTTTAGTAGAGACGGTTTCACTATGTTGGCCAGTGGAAGA ACCACGCCCTTCTAATTTTTTGTATTTTTAGTGGAGACGGTTTCACTATGTTGGCCAGTGGAAGA A G UGDH-AS1 Ensembl:ENSG00000249348 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041108107 Functional Loss SNV dbSNP153 33..33 33 - - - 2969 RMVar_ID_2969 Human_SNP_ID_180796993 A-to-I Human chr4 + 39533361 39533361 39533361 AAAATTAGCTTGGCATGGTGGTGTGCGCCTGTAGTCCCAGCTTCTCGGGAGGCTGAGGCAGGAGA AAAATTAGCTTGGCATGGTGGTGTGCGCCTGTGGTCCCAGCTTCTCGGGAGGCTGAGGCAGGAGA A G UGDH-AS1 Ensembl:ENSG00000249348 lincRNA intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,31158229,31158229 RNA-Seq:(High) rs1203559623 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5250472 2970 RMVar_ID_2970 Human_SNP_ID_180797392 A-to-I Human chr4 + 39534997 39534997 39534997 TGGAGGCGGAGGTTGCAGTGAGCCGAGATCGCACCACTGCACTCCAGCCTGGGCGTCAAAGTGAA TGGAGGCGGAGGTTGCAGTGAGCCGAGATCGCCCCACTGCACTCCAGCCTGGGCGTCAAAGTGAA A C UGDH-AS1 Ensembl:ENSG00000249348 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900425209 Functional Loss SNV dbSNP153 33..33 33 - - - 2971 RMVar_ID_2971 Human_SNP_ID_180800625 A-to-I Human chr4 - 39549008 39549008 39549008 GTATCTTTAGTAGAGATGGGGTTTCGCCATGTAGGCCAGGCTGGTCTCAAACTCCTGACCTCAGG GTATCTTTAGTAGAGATGGGGTTTCGCCATGTTGGCCAGGCTGGTCTCAAACTCCTGACCTCAGG T A SMIM14 Ensembl:ENSG00000163683 Protein coding 3'UTR GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1560278348 Functional Loss SNV dbSNP153 33..33 33 - - - 2972 RMVar_ID_2972 Human_SNP_ID_180800697 A-to-I Human chr4 - 39549320 39549320 39549320 AGATCACGCCACTGCACTCCAGCTTGAGTGACAGAGTGAGACCCTGTCTCAAAAAAAAAAGGCTT AGATCACGCCACTGCACTCCAGCTTGAGTGACGGAGTGAGACCCTGTCTCAAAAAAAAAAGGCTT T C SMIM14 Ensembl:ENSG00000163683 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1375867684 Functional Loss SNV dbSNP153 33..33 33 - - - 2973 RMVar_ID_2973 Human_SNP_ID_180800727 A-to-I Human chr4 - 39549451 39549451 39549451 TGGCCAAGACGGTGAAACCCCGTGCCTACAAAAAATTAGCCGGGTTTGGTGACACGGCCTGTAGT TGGCCAAGACGGTGAAACCCCGTGCCTACAAATAATTAGCCGGGTTTGGTGACACGGCCTGTAGT T A SMIM14 Ensembl:ENSG00000163683 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1289247161 Functional Loss SNV dbSNP153 33..33 33 - - - 2974 RMVar_ID_2974 Human_SNP_ID_180800731 A-to-I Human chr4 - 39549467 39549467 39549467 GAGGTTGAGACCAGCCTGGCCAAGACGGTGAAACCCCGTGCCTACAAAAAATTAGCCGGGTTTGG GAGGTTGAGACCAGCCTGGCCAAGACGGTGAAGCCCCGTGCCTACAAAAAATTAGCCGGGTTTGG T C SMIM14 Ensembl:ENSG00000163683 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041891510 Functional Loss SNV dbSNP153 33..33 33 - - - 2975 RMVar_ID_2975 Human_SNP_ID_180800739 A-to-I Human chr4 - 39549490 39549490 39549490 GCAGGTGGATCACTTGAGGTCAGGAGGTTGAGACCAGCCTGGCCAAGACGGTGAAACCCCGTGCC GCAGGTGGATCACTTGAGGTCAGGAGGTTGAGCCCAGCCTGGCCAAGACGGTGAAACCCCGTGCC T G SMIM14 Ensembl:ENSG00000163683 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs957945915 Functional Loss SNV dbSNP153 33..33 33 - - - 2976 RMVar_ID_2976 Human_SNP_ID_180800741 A-to-I Human chr4 - 39549501 39549501 39549501 GGGAGGCTGGGGCAGGTGGATCACTTGAGGTCAGGAGGTTGAGACCAGCCTGGCCAAGACGGTGA GGGAGGCTGGGGCAGGTGGATCACTTGAGGTCGGGAGGTTGAGACCAGCCTGGCCAAGACGGTGA T C SMIM14 Ensembl:ENSG00000163683 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs995906090 Functional Loss SNV dbSNP153 33..33 33 - - - 2977 RMVar_ID_2977 Human_SNP_ID_180800750 A-to-I Human chr4 - 39549541 39549541 39549541 AGCTGGGCGCAGTGACTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGGGGCAGGTGGATCACT AGCTGGGCGCAGTGACTCATGCCTGTAATCCCGGCACTTTGGGAGGCTGGGGCAGGTGGATCACT T C SMIM14 Ensembl:ENSG00000163683 Protein coding 3'UTR GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs575076147 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_555345 2978 RMVar_ID_2978 Human_SNP_ID_180800928 A-to-I Human chr4 - 39550438 39550438 39550438 ATCTCTACTAAAAATGCAAAAATTAGCCAGGCATGGTGGTGTGTGCCTATAATCCCAGCTACTGG ATCTCTACTAAAAATGCAAAAATTAGCCAGGCGTGGTGGTGTGTGCCTATAATCCCAGCTACTGG T C SMIM14 Ensembl:ENSG00000163683 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs897556978 Functional Loss SNV dbSNP153 33..33 33 - - - 2979 RMVar_ID_2979 Human_SNP_ID_180800948 A-to-I Human chr4 - 39550555 39550555 39550555 TGCATGGGCTGGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGCGA TGCATGGGCTGGGCACGGTGGCTCACGCCTGTCATCCCAGCACTTTGGGAGGCCGAGGCAGGCGA T G SMIM14 Ensembl:ENSG00000163683 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs977375346 Functional Loss SNV dbSNP153 33..33 33 - - - 2980 RMVar_ID_2980 Human_SNP_ID_180800954 A-to-I Human chr4 - 39550563 39550563 39550563 AAAATGTCTGCATGGGCTGGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAG AAAATGTCTGCATGGGCTGGGCACGGTGGCTCGCGCCTGTAATCCCAGCACTTTGGGAGGCCGAG T C SMIM14 Ensembl:ENSG00000163683 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1361717140 Functional Loss SNV dbSNP153 33..33 33 - - - 2981 RMVar_ID_2981 Human_SNP_ID_180803368 A-to-I Human chr4 - 39561483 39561482 39561483 TGGCTGGGCATGACTACTGACTGACACCTGTAATCTCAGCTCTTTGGGAAACCAAGGCAGGAGGA TGGCTGGGCATGACTACTGACTGACACCTGTA_TCTCAGCTCTTTGGGAAACCAAGGCAGGAGGA AT A SMIM14 Ensembl:ENSG00000163683 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277628710 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_354699,RMVar_hsa_circ_340671 2982 RMVar_ID_2982 Human_SNP_ID_180810488 A-to-I Human chr4 - 39591767 39591767 39591767 GAGGCCAGGAGTTTGAGACCAACCTGGCCAACATGGTGAAACCCTGTTGGTAGTAGTCTCTACTA GAGGCCAGGAGTTTGAGACCAACCTGGCCAACGTGGTGAAACCCTGTTGGTAGTAGTCTCTACTA T C SMIM14 Ensembl:ENSG00000163683 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910955984 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_354699,RMVar_hsa_circ_333996 2983 RMVar_ID_2983 Human_SNP_ID_180813516 A-to-I Human chr4 - 39604386 39604386 39604386 ACTACAGGAGTGTGCCACCACGCCTGGCTAATATTTGCATTTTTAGTAGAGACTGGGTTTCACCA ACTACAGGAGTGTGCCACCACGCCTGGCTAATGTTTGCATTTTTAGTAGAGACTGGGTTTCACCA T C SMIM14 Ensembl:ENSG00000163683 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1274508311 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_354699,RMVar_hsa_circ_333996 2984 RMVar_ID_2984 Human_SNP_ID_180813529 A-to-I Human chr4 - 39604455 39604455 39604455 TCGGCTCACTACAGCCTCCACCTCCTGAGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAAC TCGGCTCACTACAGCCTCCACCTCCTGAGTTCCAGCGATTCTCCTGCCTCAGCCTCCCGAGTAAC T G SMIM14 Ensembl:ENSG00000163683 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs951100791 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_354699,RMVar_hsa_circ_333996 2985 RMVar_ID_2985 Human_SNP_ID_180814853 A-to-I Human chr4 - 39610259 39610259 39610259 AATTGGACCAGGCGCGGTGGCTCACACCTGTAATTTCAGCACTTTGGGAGGCTGAGGAGGGAGGA AATTGGACCAGGCGCGGTGGCTCACACCTGTAGTTTCAGCACTTTGGGAGGCTGAGGAGGGAGGA T C SMIM14 Ensembl:ENSG00000163683 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1295825965 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_300649,RMVar_hsa_circ_225458 2986 RMVar_ID_2986 Human_SNP_ID_180816906 A-to-I Human chr4 - 39619080 39619080 39619080 TTTTCTCTTGAACTGAACATGCTAAATTATCTAAACCCTGTCTTACCCTCTATCATCACTTAATT TTTTCTCTTGAACTGAACATGCTAAATTATCTGAACCCTGTCTTACCCTCTATCATCACTTAATT T C SMIM14 Ensembl:ENSG00000163683 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs901683247 Functional Loss SNV dbSNP153 33..33 33 - - - 2987 RMVar_ID_2987 Human_SNP_ID_180838446 A-to-I Human chr4 + 39703277 39703276 39703277 TGGGGTGGCTTATGCCTGTAATCTAGCATTTTAGGAGGCTGAGACTCGATTGAGGCCAGGAGTTC TGGGGTGGCTTATGCCTGTAATCTAGCATTTT_GGAGGCTGAGACTCGATTGAGGCCAGGAGTTC TA T UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1427767036 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_7308693,Human_RBP_ID_8591204,Human_RBP_ID_15147245 2988 RMVar_ID_2988 Human_SNP_ID_180838695 A-to-I Human chr4 + 39704176 39704176 39704176 ACTTGGGGAGGCTGAGGCAGGAGAATCGTTTGAGTCTGGGAGGTCGAGGCTGCAGTGAGCGGTGA ACTTGGGGAGGCTGAGGCAGGAGAATCGTTTGCGTCTGGGAGGTCGAGGCTGCAGTGAGCGGTGA A C UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1231050682 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7308703 2989 RMVar_ID_2989 Human_SNP_ID_180838782 A-to-I Human chr4 + 39704588 39704588 39704588 TTTTGAAACAGAGTCTCACTGTCACCAAAGCTAGAATGCAGTGGCGTGATCACAGTTCACTGCAG TTTTGAAACAGAGTCTCACTGTCACCAAAGCTGGAATGCAGTGGCGTGATCACAGTTCACTGCAG A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,cerebellum - 29129909,30559470 RNA-Seq:(High) rs538108231 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15147304 2990 RMVar_ID_2990 Human_SNP_ID_180838794 A-to-I Human chr4 + 39704653 39704653 39704653 CCTTGAACTCCCCAGGCTTAGATGATCCTCCTACCTCAGCCTTCCAAGTAGCAGGGACTAAAGGC CCTTGAACTCCCCAGGCTTAGATGATCCTCCTGCCTCAGCCTTCCAAGTAGCAGGGACTAAAGGC A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1353462951 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15147308 2991 RMVar_ID_2991 Human_SNP_ID_180839035 A-to-I Human chr4 + 39705275 39705275 39705275 GCTGGAGTATGGTGGCACGATCTCAACTCACCACAGCCTCTGCCTCCCGGGTTCAAGCGACTCTC GCTGGAGTATGGTGGCACGATCTCAACTCACCGCAGCCTCTGCCTCCCGGGTTCAAGCGACTCTC A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,frontal_cortex - 29129909,30559470 RNA-Seq:(High) rs1320196828 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7308717,Human_RBP_ID_9160083,Human_RBP_ID_15147342,Human_RBP_ID_25809300 2992 RMVar_ID_2992 Human_SNP_ID_180839153 A-to-I Human chr4 + 39705724 39705724 39705724 TTGTTTTGTTTTTGTGACAGAGTCTCGGCTCTATCACCCAGCCTGGAGTGCAGTGGCTCCATCTC TTGTTTTGTTTTTGTGACAGAGTCTCGGCTCTGTCACCCAGCCTGGAGTGCAGTGGCTCCATCTC A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs549846801 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2846057,Human_RBP_ID_7308724,Human_RBP_ID_15147364 2993 RMVar_ID_2993 Human_SNP_ID_180839711 A-to-I Human chr4 + 39707772 39707772 39707772 GAACTCCTGGCTTCAAGCAGTCCTCCTGCCTCAGCCTCCCAAAGTGCTGGGATTATAGGCATGAG GAACTCCTGGCTTCAAGCAGTCCTCCTGCCTCGGCCTCCCAAAGTGCTGGGATTATAGGCATGAG A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs542108031 Functional Loss SNV dbSNP153 33..33 33 - - - 2994 RMVar_ID_2994 Human_SNP_ID_180840731 A-to-I Human chr4 + 39711884 39711884 39711884 CCATGGAGAAACCTCGTCTCTCTACTAAAAATACAAAAAATTAGCCAGGCATGGTGGTGCATGCC CCATGGAGAAACCTCGTCTCTCTACTAAAAATGCAAAAAATTAGCCAGGCATGGTGGTGCATGCC A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1297835977 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_225460,RMVar_hsa_circ_225462,RMVar_hsa_circ_225461,RMVar_hsa_circ_225459 2995 RMVar_ID_2995 Human_SNP_ID_180840966 A-to-I Human chr4 + 39712488 39712488 39712488 CTCTCGCTTTATCGCCCAGGCTGGAGTACAGTAGCACAATCTTGGCTCATTGCAACCTCCATCTC CTCTCGCTTTATCGCCCAGGCTGGAGTACAGTGGCACAATCTTGGCTCATTGCAACCTCCATCTC A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1444681641 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15147699 RMVar_hsa_circ_225460,RMVar_hsa_circ_225462,RMVar_hsa_circ_225461,RMVar_hsa_circ_225459 2996 RMVar_ID_2996 Human_SNP_ID_180840970 A-to-I Human chr4 + 39712504 39712504 39712504 CAGGCTGGAGTACAGTAGCACAATCTTGGCTCATTGCAACCTCCATCTCCTGTGTTCAAGCAATT CAGGCTGGAGTACAGTAGCACAATCTTGGCTCGTTGCAACCTCCATCTCCTGTGTTCAAGCAATT A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1359332795 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_225460,RMVar_hsa_circ_225462,RMVar_hsa_circ_225461,RMVar_hsa_circ_225459 2997 RMVar_ID_2997 Human_SNP_ID_180842578 A-to-I Human chr4 + 39717396 39717396 39717396 GGGATTACAGATGCATGCTGCCACACCCGGCTAATTTTTGTGTTTTAAGTACAGACAGGGTTTCA GGGATTACAGATGCATGCTGCCACACCCGGCTGATTTTTGTGTTTTAAGTACAGACAGGGTTTCA A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1302888374 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15147937,Human_RBP_ID_21044887 RMVar_hsa_circ_225460,RMVar_hsa_circ_225462,RMVar_hsa_circ_225461,RMVar_hsa_circ_225464,RMVar_hsa_circ_225459,RMVar_hsa_circ_225463 2998 RMVar_ID_2998 Human_SNP_ID_180843829 A-to-I Human chr4 + 39721833 39721833 39721833 TCTTTTGGTTGGGCATGGTGGCTCACTCTGGTAATCCTTGCACTTTAGGAGGCTGAGGCAGGAGG TCTTTTGGTTGGGCATGGTGGCTCACTCTGGTGATCCTTGCACTTTAGGAGGCTGAGGCAGGAGG A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE47997;GSE38233;GSE38233;GSE100210;GSE107867;GSE107867 K562 cells&HepG2 cells;cultured B-cells;cultured B-cells;HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank;ASD brains,Fragile X samples from NIH NeuroBioBank - 23474544,24183664,24183664,29129909,30559470,30559470 RNA-Seq:(High) rs1241969545 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15148093 RMVar_hsa_circ_225460,RMVar_hsa_circ_225462,RMVar_hsa_circ_225461,RMVar_hsa_circ_225465,RMVar_hsa_circ_225464,RMVar_hsa_circ_225459,RMVar_hsa_circ_225463 2999 RMVar_ID_2999 Human_SNP_ID_180844055 A-to-I Human chr4 + 39722753 39722753 39722753 GTGTGGGATTTTTTTTTCCTCATAAATGTTATAAGGAAATGATGTTATCCAAGGACCTGCTGTAT GTGTGGGATTTTTTTTTCCTCATAAATGTTATGAGGAAATGATGTTATCCAAGGACCTGCTGTAT A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946747010 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1978520,Human_RBP_ID_8591234,Human_RBP_ID_15148137 RMVar_hsa_circ_225460,RMVar_hsa_circ_225462,RMVar_hsa_circ_225461,RMVar_hsa_circ_225465,RMVar_hsa_circ_225464,RMVar_hsa_circ_225459,RMVar_hsa_circ_225463 3000 RMVar_ID_3000 Human_SNP_ID_180844503 A-to-I Human chr4 + 39724242 39724242 39724242 TGATCCTCCAACCTCAGCCTCCCAAGTAGCTGAGACTATAGGCACGCACCACCACACCTGGCTAA TGATCCTCCAACCTCAGCCTCCCAAGTAGCTGCGACTATAGGCACGCACCACCACACCTGGCTAA A C UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1044703523 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_225460,RMVar_hsa_circ_225462,RMVar_hsa_circ_225461,RMVar_hsa_circ_225465,RMVar_hsa_circ_225464,RMVar_hsa_circ_225459,RMVar_hsa_circ_225463 3001 RMVar_ID_3001 Human_SNP_ID_180844650 A-to-I Human chr4 + 39724640 39724640 39724640 AAATACAAAAATTAGCTAGGCATGGTAAGTGCATGCCTGTAGGCCCAGCTACTTGGGGGGGCTGA AAATACAAAAATTAGCTAGGCATGGTAAGTGCTTGCCTGTAGGCCCAGCTACTTGGGGGGGCTGA A T UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1423790861 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17574739 RMVar_hsa_circ_225460,RMVar_hsa_circ_225462,RMVar_hsa_circ_225461,RMVar_hsa_circ_225465,RMVar_hsa_circ_225464,RMVar_hsa_circ_225459,RMVar_hsa_circ_225463 3002 RMVar_ID_3002 Human_SNP_ID_180844795 A-to-I Human chr4 + 39725152 39725152 39725152 ATTGTAATCCCAGCACTTTGGGAGTCCAAGGCAGACAGATTGCTTTAGCCCAAGAATTTGAGATT ATTGTAATCCCAGCACTTTGGGAGTCCAAGGCGGACAGATTGCTTTAGCCCAAGAATTTGAGATT A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1464652233 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15148241 RMVar_hsa_circ_225460,RMVar_hsa_circ_225462,RMVar_hsa_circ_225461,RMVar_hsa_circ_225465,RMVar_hsa_circ_225464,RMVar_hsa_circ_225459,RMVar_hsa_circ_225463 3003 RMVar_ID_3003 Human_SNP_ID_180844808 A-to-I Human chr4 + 39725218 39725218 39725218 GTAGACAAATGGAGACATGGCGAACCGTCTCTACAGAAAATACAAATATTAACCAGGCATGGTGT GTAGACAAATGGAGACATGGCGAACCGTCTCTGCAGAAAATACAAATATTAACCAGGCATGGTGT A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs561941548 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15148248,Human_RBP_ID_17574613 RMVar_hsa_circ_225460,RMVar_hsa_circ_225462,RMVar_hsa_circ_225461,RMVar_hsa_circ_225465,RMVar_hsa_circ_225464,RMVar_hsa_circ_225459,RMVar_hsa_circ_225463 3004 RMVar_ID_3004 Human_SNP_ID_180844809 A-to-I Human chr4 + 39725227 39725227 39725227 TGGAGACATGGCGAACCGTCTCTACAGAAAATACAAATATTAACCAGGCATGGTGTCATGCACCT TGGAGACATGGCGAACCGTCTCTACAGAAAATGCAAATATTAACCAGGCATGGTGTCATGCACCT A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs778146620 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17574613 RMVar_hsa_circ_225460,RMVar_hsa_circ_225462,RMVar_hsa_circ_225461,RMVar_hsa_circ_225465,RMVar_hsa_circ_225464,RMVar_hsa_circ_225459,RMVar_hsa_circ_225463 3005 RMVar_ID_3005 Human_SNP_ID_180844814 A-to-I Human chr4 + 39725244 39725244 39725244 GTCTCTACAGAAAATACAAATATTAACCAGGCATGGTGTCATGCACCTGTACTCACAGCTACTCA GTCTCTACAGAAAATACAAATATTAACCAGGCGTGGTGTCATGCACCTGTACTCACAGCTACTCA A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1290182118 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17574741 RMVar_hsa_circ_225460,RMVar_hsa_circ_225462,RMVar_hsa_circ_225461,RMVar_hsa_circ_225465,RMVar_hsa_circ_225464,RMVar_hsa_circ_225459,RMVar_hsa_circ_225463 3006 RMVar_ID_3006 Human_SNP_ID_180845034 A-to-I Human chr4 + 39725890 39725890 39725890 GTCTTGAACTCCTGGGCTCAAGCAGTCTGTCCACCTTGGCCTTCCAAAGTGTTGGGATTACAGGC GTCTTGAACTCCTGGGCTCAAGCAGTCTGTCCTCCTTGGCCTTCCAAAGTGTTGGGATTACAGGC A T UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1248207897 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15148280 RMVar_hsa_circ_225460,RMVar_hsa_circ_225462,RMVar_hsa_circ_225461,RMVar_hsa_circ_225465,RMVar_hsa_circ_225464,RMVar_hsa_circ_225459,RMVar_hsa_circ_225463 3007 RMVar_ID_3007 Human_SNP_ID_180845217 A-to-I Human chr4 + 39726651 39726651 39726651 ATGGAGTCTCACTGTCTCCCAGGCTGGAGTGCAATGGTGCGATCTCGGCTTACTGCAACCTCTGC ATGGAGTCTCACTGTCTCCCAGGCTGGAGTGCGATGGTGCGATCTCGGCTTACTGCAACCTCTGC A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1242084037 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_225460,RMVar_hsa_circ_225462,RMVar_hsa_circ_225461,RMVar_hsa_circ_225465,RMVar_hsa_circ_225464,RMVar_hsa_circ_225459,RMVar_hsa_circ_225463 3008 RMVar_ID_3008 Human_SNP_ID_180846221 A-to-I Human chr4 + 39730302 39730302 39730302 GACCTCTTGGGCTCAAGTGATTCTCCCACTTCAACTTCCTGAATAGCTGGGATTACAGACACACG GACCTCTTGGGCTCAAGTGATTCTCCCACTTCGACTTCCTGAATAGCTGGGATTACAGACACACG A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1295112213 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_225460,RMVar_hsa_circ_225462,RMVar_hsa_circ_225461,RMVar_hsa_circ_225465,RMVar_hsa_circ_225464,RMVar_hsa_circ_225459,RMVar_hsa_circ_225463 3009 RMVar_ID_3009 Human_SNP_ID_180846871 A-to-I Human chr4 + 39732865 39732864 39732866 GCCCAGTTAATTTTTGTATTTGTAGTAGAGACAGGGTTTTGCCATATGGGCCAGGCTGGTCTCAA GCCCAGTTAATTTTTGTATTTGTAGTAGAGAC__GGTTTTGCCATATGGGCCAGGCTGGTCTCAA CAG C UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1288591677 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_15148571 RMVar_hsa_circ_225460,RMVar_hsa_circ_225462,RMVar_hsa_circ_225461,RMVar_hsa_circ_225465,RMVar_hsa_circ_225464,RMVar_hsa_circ_225459,RMVar_hsa_circ_225463 3010 RMVar_ID_3010 Human_SNP_ID_180846872 A-to-I Human chr4 + 39732865 39732865 39732865 GCCCAGTTAATTTTTGTATTTGTAGTAGAGACAGGGTTTTGCCATATGGGCCAGGCTGGTCTCAA GCCCAGTTAATTTTTGTATTTGTAGTAGAGACGGGGTTTTGCCATATGGGCCAGGCTGGTCTCAA A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1327970435 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15148571 RMVar_hsa_circ_225460,RMVar_hsa_circ_225462,RMVar_hsa_circ_225461,RMVar_hsa_circ_225465,RMVar_hsa_circ_225464,RMVar_hsa_circ_225459,RMVar_hsa_circ_225463 3011 RMVar_ID_3011 Human_SNP_ID_180847248 A-to-I Human chr4 + 39734161 39734161 39734161 AGAGTCTCACTGTGTTACCCAAACTGGAGTGCAATGGCGAAATCTCGGCTCACTCCAACCTCCAC AGAGTCTCACTGTGTTACCCAAACTGGAGTGCGATGGCGAAATCTCGGCTCACTCCAACCTCCAC A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1320805276 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15148625 RMVar_hsa_circ_225460,RMVar_hsa_circ_225462,RMVar_hsa_circ_225461,RMVar_hsa_circ_225465,RMVar_hsa_circ_225464,RMVar_hsa_circ_225459,RMVar_hsa_circ_225463,RMVar_hsa_circ_225468,RMVar_hsa_circ_225467 3012 RMVar_ID_3012 Human_SNP_ID_180847280 A-to-I Human chr4 + 39734247 39734247 39734247 CGTGCCTCAACCTCCCAAGTAGCGGGGACTACAGGCACACACCACCATGCCCGGCTAATTTTTCC CGTGCCTCAACCTCCCAAGTAGCGGGGACTACGGGCACACACCACCATGCCCGGCTAATTTTTCC A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs901026735 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_225460,RMVar_hsa_circ_225462,RMVar_hsa_circ_225461,RMVar_hsa_circ_225465,RMVar_hsa_circ_225464,RMVar_hsa_circ_225459,RMVar_hsa_circ_225463,RMVar_hsa_circ_225468,RMVar_hsa_circ_225467 3013 RMVar_ID_3013 Human_SNP_ID_180847381 A-to-I Human chr4 + 39734632 39734632 39734632 CAGGAGTTCAAGACCAGCCTGAGAAACATGGCAAAACCCCCTCTCTACTAAAAATTTAAAACTTT CAGGAGTTCAAGACCAGCCTGAGAAACATGGCCAAACCCCCTCTCTACTAAAAATTTAAAACTTT A C UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1407135439 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_225460,RMVar_hsa_circ_225462,RMVar_hsa_circ_225461,RMVar_hsa_circ_225465,RMVar_hsa_circ_225464,RMVar_hsa_circ_225459,RMVar_hsa_circ_225463,RMVar_hsa_circ_225468,RMVar_hsa_circ_225467 3014 RMVar_ID_3014 Human_SNP_ID_180847565 A-to-I Human chr4 + 39735309 39735308 39735309 TTGGCTCATTGCAACCTCCGTCTCCCTGGTTCAAGTGATTCTCCTGCCTCAGCTTCCCGAGTAGC TTGGCTCATTGCAACCTCCGTCTCCCTGGTTC_AGTGATTCTCCTGCCTCAGCTTCCCGAGTAGC CA C UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1244678343 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_225460,RMVar_hsa_circ_225462,RMVar_hsa_circ_225461,RMVar_hsa_circ_225465,RMVar_hsa_circ_225464,RMVar_hsa_circ_225459,RMVar_hsa_circ_225463,RMVar_hsa_circ_225468,RMVar_hsa_circ_225467 3015 RMVar_ID_3015 Human_SNP_ID_180847566 A-to-I Human chr4 + 39735309 39735309 39735309 TTGGCTCATTGCAACCTCCGTCTCCCTGGTTCAAGTGATTCTCCTGCCTCAGCTTCCCGAGTAGC TTGGCTCATTGCAACCTCCGTCTCCCTGGTTCGAGTGATTCTCCTGCCTCAGCTTCCCGAGTAGC A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1204079248 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_225460,RMVar_hsa_circ_225462,RMVar_hsa_circ_225461,RMVar_hsa_circ_225465,RMVar_hsa_circ_225464,RMVar_hsa_circ_225459,RMVar_hsa_circ_225463,RMVar_hsa_circ_225468,RMVar_hsa_circ_225467 3016 RMVar_ID_3016 Human_SNP_ID_180847862 A-to-I Human chr4 + 39736347 39736347 39736347 AGCTGAGCATGGTAGTGGGTGCCTGTAATCCCAGCTACTCAGGAGGCTGAAGCAGGAGAGTCACT AGCTGAGCATGGTAGTGGGTGCCTGTAATCCCGGCTACTCAGGAGGCTGAAGCAGGAGAGTCACT A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1274170314 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_225460,RMVar_hsa_circ_225462,RMVar_hsa_circ_225461,RMVar_hsa_circ_225465,RMVar_hsa_circ_225464,RMVar_hsa_circ_225459,RMVar_hsa_circ_225463,RMVar_hsa_circ_225468,RMVar_hsa_circ_225467 3017 RMVar_ID_3017 Human_SNP_ID_180848440 A-to-I Human chr4 + 39738864 39738864 39738864 TGCCGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACAATAACGGCCAGGCTGGTCTTGA TGCCGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACAATAACGGCCAGGCTGGTCTTGA A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs988728362 Functional Loss SNV dbSNP153 33..33 33 - - - 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_225469 3018 RMVar_ID_3018 Human_SNP_ID_180848462 A-to-I Human chr4 + 39738943 39738927 39738943 GTGATCCGCCTGTCTTGGCCTCCCAAAGTGTTAGGATTACAGGCGTGAGCCACCAATCCCGGCCA GTGATCCGCCTGTCTTG________________GGATTACAGGCGTGAGCCACCAATCCCGGCCA GGCCTCCCAAAGTGTTA G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1287166247 Functional Loss DEL dbSNP153 18..33 33 - - - Human_RBP_ID_17574972 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_225469 3019 RMVar_ID_3019 Human_SNP_ID_180848916 A-to-I Human chr4 + 39740427 39740412 39740427 AGCCGGGCGAGGTGGTGGGCGCCTGTGGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCG AGCCGGGCGAGGTGGTGG_______________GCTACTCGGGAGGCTGAGGCAGGAGAATGGCG GGCGCCTGTGGTCCCA G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1398023193 Functional Loss DEL dbSNP153 19..33 33 - - - 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_225469 3020 RMVar_ID_3020 Human_SNP_ID_180848921 A-to-I Human chr4 + 39740427 39740427 39740427 AGCCGGGCGAGGTGGTGGGCGCCTGTGGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCG AGCCGGGCGAGGTGGTGGGCGCCTGTGGTCCCGGCTACTCGGGAGGCTGAGGCAGGAGAATGGCG A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs972858087 Functional Loss SNV dbSNP153 33..33 33 - - - 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_225469 3021 RMVar_ID_3021 Human_SNP_ID_180849190 A-to-I Human chr4 + 39741148 39741148 39741148 CAAAAATTAGCTGGGTGTGGTGGCGTGCGCCTATAATCCCAGCTACTCAGGAGGCTGAGGCAGGA CAAAAATTAGCTGGGTGTGGTGGCGTGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGA A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs959366155 Functional Loss SNV dbSNP153 33..33 33 - - - 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_225469 3022 RMVar_ID_3022 Human_SNP_ID_180849191 A-to-I Human chr4 + 39741150 39741150 39741150 AAAATTAGCTGGGTGTGGTGGCGTGCGCCTATAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA AAAATTAGCTGGGTGTGGTGGCGTGCGCCTATGATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs545699919 Functional Loss SNV dbSNP153 33..33 33 - - - 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_225469 3023 RMVar_ID_3023 Human_SNP_ID_180849193 A-to-I Human chr4 + 39741160 39741160 39741160 GGGTGTGGTGGCGTGCGCCTATAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCCCTTGAA GGGTGTGGTGGCGTGCGCCTATAATCCCAGCTGCTCAGGAGGCTGAGGCAGGAGAATCCCTTGAA A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs527916249 Functional Loss SNV dbSNP153 33..33 33 - - - 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_225469 3024 RMVar_ID_3024 Human_SNP_ID_180849933 A-to-I Human chr4 + 39743902 39743902 39743902 TCTGTTTATTTGAGATAGATTCTTGCTCTGTCACGTAGGCTGGAGTGCAGTGGTGCGAACTTGGC TCTGTTTATTTGAGATAGATTCTTGCTCTGTCCCGTAGGCTGGAGTGCAGTGGTGCGAACTTGGC A C UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs919142885 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15148896 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_225469 3025 RMVar_ID_3025 Human_SNP_ID_180849953 A-to-I Human chr4 + 39743962 39743962 39743962 TTGGCTCATTGCAATATCCACCTCCTGGGTTCAAGCGATTCTTGTGCCTCAACCTCCTGAGTAGC TTGGCTCATTGCAATATCCACCTCCTGGGTTCGAGCGATTCTTGTGCCTCAACCTCCTGAGTAGC A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs923707166 Functional Loss SNV dbSNP153 33..33 33 - - - 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_225469 3026 RMVar_ID_3026 Human_SNP_ID_180849990 A-to-I Human chr4 + 39744115 39744115 39744115 GAACTTCTGGCGTCAAGTGATCTGCCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAG GAACTTCTGGCGTCAAGTGATCTGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAG A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1347446422 Functional Loss SNV dbSNP153 33..33 33 - - - 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_225469 3027 RMVar_ID_3027 Human_SNP_ID_180850299 A-to-I Human chr4 + 39745113 39745113 39745113 AAACTCCTGGCCTAGCTTTAAGCAGTCCTCCCACCTCGGCCTCCCAAAGTGTTGGGATTACAAGG AAACTCCTGGCCTAGCTTTAAGCAGTCCTCCCTCCTCGGCCTCCCAAAGTGTTGGGATTACAAGG A T UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1457562791 Functional Loss SNV dbSNP153 33..33 33 - - - 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_225469 3028 RMVar_ID_3028 Human_SNP_ID_180851108 A-to-I Human chr4 + 39748522 39748522 39748522 TGTTACCTGGCCAGGCATGGTGGCTCACGCCTATAATCCCAGCACTTTAGGAAGTCAAGGCAGGA TGTTACCTGGCCAGGCATGGTGGCTCACGCCTGTAATCCCAGCACTTTAGGAAGTCAAGGCAGGA A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs548589478 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17574614 RMVar_hsa_circ_225460,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_225472,RMVar_hsa_circ_271227,RMVar_hsa_circ_225471,RMVar_hsa_circ_225474,RMVar_hsa_circ_287533,RMVar_hsa_circ_313227,RMVar_hsa_circ_289256,RMVar_hsa_circ_225475,RMVar_hsa_circ_225473 3029 RMVar_ID_3029 Human_SNP_ID_180851374 A-to-I Human chr4 + 39749558 39749555 39749558 AATACTAGTCTGGTATGGTGGCATGCGCCTGTAGTCTCAGCTACTCAGGAGGCTAAGGCACAAGA AATACTAGTCTGGTATGGTGGCATGCGCCT___GTCTCAGCTACTCAGGAGGCTAAGGCACAAGA TGTA T UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1272026511 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_15149042 RMVar_hsa_circ_225460,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_225472,RMVar_hsa_circ_271227,RMVar_hsa_circ_225471,RMVar_hsa_circ_225474,RMVar_hsa_circ_287533,RMVar_hsa_circ_313227,RMVar_hsa_circ_289256,RMVar_hsa_circ_225475,RMVar_hsa_circ_225473 3030 RMVar_ID_3030 Human_SNP_ID_180851377 A-to-I Human chr4 + 39749558 39749558 39749558 AATACTAGTCTGGTATGGTGGCATGCGCCTGTAGTCTCAGCTACTCAGGAGGCTAAGGCACAAGA AATACTAGTCTGGTATGGTGGCATGCGCCTGTGGTCTCAGCTACTCAGGAGGCTAAGGCACAAGA A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs534931393 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15149042 RMVar_hsa_circ_225460,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_225472,RMVar_hsa_circ_271227,RMVar_hsa_circ_225471,RMVar_hsa_circ_225474,RMVar_hsa_circ_287533,RMVar_hsa_circ_313227,RMVar_hsa_circ_289256,RMVar_hsa_circ_225475,RMVar_hsa_circ_225473 3031 RMVar_ID_3031 Human_SNP_ID_180851699 A-to-I Human chr4 + 39750799 39750799 39750799 ACAGGGTCTTGCTGTGTTGCCCAGGCTGGAGTACAGTGGCATGATCATGGCTCACTGCAACCTCT ACAGGGTCTTGCTGTGTTGCCCAGGCTGGAGTCCAGTGGCATGATCATGGCTCACTGCAACCTCT A C UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1217001010 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25809776 RMVar_hsa_circ_225460,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_225472,RMVar_hsa_circ_271227,RMVar_hsa_circ_225471,RMVar_hsa_circ_225474,RMVar_hsa_circ_287533,RMVar_hsa_circ_313227,RMVar_hsa_circ_289256,RMVar_hsa_circ_225475,RMVar_hsa_circ_225473 3032 RMVar_ID_3032 Human_SNP_ID_180851802 A-to-I Human chr4 + 39751217 39751217 39751217 CACCTGCCTTGGCTTCCCAAACTGCTAGGATTATAGACATGAGCCACCATTCCCAGCCCAAATTC CACCTGCCTTGGCTTCCCAAACTGCTAGGATTGTAGACATGAGCCACCATTCCCAGCCCAAATTC A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350529467 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7309142,Human_RBP_ID_15149071 RMVar_hsa_circ_225460,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_225472,RMVar_hsa_circ_271227,RMVar_hsa_circ_225471,RMVar_hsa_circ_225474,RMVar_hsa_circ_287533,RMVar_hsa_circ_313227,RMVar_hsa_circ_289256,RMVar_hsa_circ_225475,RMVar_hsa_circ_225473 3033 RMVar_ID_3033 Human_SNP_ID_180851884 A-to-I Human chr4 + 39751536 39751536 39751536 TCTTGTGTCCACAAAAAATATGAAAATTAGCCAGGAGTGATGGCGCACGCCTGTAGTCCCAACTA TCTTGTGTCCACAAAAAATATGAAAATTAGCCGGGAGTGATGGCGCACGCCTGTAGTCCCAACTA A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1214525481 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15149077,Human_RBP_ID_25809786 RMVar_hsa_circ_225460,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_225472,RMVar_hsa_circ_271227,RMVar_hsa_circ_225471,RMVar_hsa_circ_225476,RMVar_hsa_circ_225474,RMVar_hsa_circ_287533,RMVar_hsa_circ_313227,RMVar_hsa_circ_289256,RMVar_hsa_circ_225475,RMVar_hsa_circ_225473 3034 RMVar_ID_3034 Human_SNP_ID_180851901 A-to-I Human chr4 + 39751568 39751568 39751568 AGGAGTGATGGCGCACGCCTGTAGTCCCAACTACTCAGGAGGCTGAGGCAGAAGAATTGAGCTCA AGGAGTGATGGCGCACGCCTGTAGTCCCAACTTCTCAGGAGGCTGAGGCAGAAGAATTGAGCTCA A T UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1374093418 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7309145,Human_RBP_ID_17574975,Human_RBP_ID_25809790 RMVar_hsa_circ_225460,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_225472,RMVar_hsa_circ_271227,RMVar_hsa_circ_225471,RMVar_hsa_circ_225476,RMVar_hsa_circ_225474,RMVar_hsa_circ_287533,RMVar_hsa_circ_313227,RMVar_hsa_circ_289256,RMVar_hsa_circ_225475,RMVar_hsa_circ_225473 3035 RMVar_ID_3035 Human_SNP_ID_180851973 A-to-I Human chr4 + 39751816 39751816 39751816 GGTGAAACCCTGTCACTACTAAAAAATAGAAAAATTAGTCGGGTGTGGTGGCGCACACACGTAGT GGTGAAACCCTGTCACTACTAAAAAATAGAAAGATTAGTCGGGTGTGGTGGCGCACACACGTAGT A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1000200055 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_225460,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_225472,RMVar_hsa_circ_271227,RMVar_hsa_circ_225471,RMVar_hsa_circ_225476,RMVar_hsa_circ_225474,RMVar_hsa_circ_287533,RMVar_hsa_circ_313227,RMVar_hsa_circ_289256,RMVar_hsa_circ_225475,RMVar_hsa_circ_225473 3036 RMVar_ID_3036 Human_SNP_ID_180852085 A-to-I Human chr4 + 39752219 39752219 39752219 CAGTGGCACGATCTCAGCTCACTGCAAGCTCCATCTCCCTTTACGCCATTCTCCTGCCTCAGCCA CAGTGGCACGATCTCAGCTCACTGCAAGCTCCGTCTCCCTTTACGCCATTCTCCTGCCTCAGCCA A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1305401679 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7309153,Human_RBP_ID_15149088 RMVar_hsa_circ_225460,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_225472,RMVar_hsa_circ_271227,RMVar_hsa_circ_225471,RMVar_hsa_circ_225476,RMVar_hsa_circ_225474,RMVar_hsa_circ_287533,RMVar_hsa_circ_313227,RMVar_hsa_circ_289256,RMVar_hsa_circ_225475,RMVar_hsa_circ_225473 3037 RMVar_ID_3037 Human_SNP_ID_180852347 A-to-I Human chr4 + 39752891 39752891 39752891 ACTCAGCATGGGCCAAGCACTGTGGCCCACTCATGCCTGTAATCCCAGCAGTTTGGGAGGCCGAG ACTCAGCATGGGCCAAGCACTGTGGCCCACTCGTGCCTGTAATCCCAGCAGTTTGGGAGGCCGAG A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs371793609 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17574748 RMVar_hsa_circ_225460,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_225472,RMVar_hsa_circ_271227,RMVar_hsa_circ_225471,RMVar_hsa_circ_225476,RMVar_hsa_circ_225474,RMVar_hsa_circ_287533,RMVar_hsa_circ_313227,RMVar_hsa_circ_289256,RMVar_hsa_circ_225475,RMVar_hsa_circ_225473 3038 RMVar_ID_3038 Human_SNP_ID_180852413 A-to-I Human chr4 + 39753131 39753131 39753131 AATGTTTGATGTGGGCTCAGTGGCTCACGCCTATAATCCTAGTACTTTGGGAGCCTATGTCGGGT AATGTTTGATGTGGGCTCAGTGGCTCACGCCTGTAATCCTAGTACTTTGGGAGCCTATGTCGGGT A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1018233737 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_225460,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_225472,RMVar_hsa_circ_271227,RMVar_hsa_circ_225471,RMVar_hsa_circ_225476,RMVar_hsa_circ_225474,RMVar_hsa_circ_287533,RMVar_hsa_circ_313227,RMVar_hsa_circ_289256,RMVar_hsa_circ_225475,RMVar_hsa_circ_225473 3039 RMVar_ID_3039 Human_SNP_ID_180854164 A-to-I Human chr4 + 39759942 39759942 39759942 TCATGCCTGTTATCCCAACACTTTGGGAGGCCAAGGTAGGTGGATTGCTTGAGGTCAGGAGTTCA TCATGCCTGTTATCCCAACACTTTGGGAGGCCGAGGTAGGTGGATTGCTTGAGGTCAGGAGTTCA A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs981038102 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_225460,RMVar_hsa_circ_225465,RMVar_hsa_circ_225464,RMVar_hsa_circ_225459,RMVar_hsa_circ_225463,RMVar_hsa_circ_225468,RMVar_hsa_circ_298369,RMVar_hsa_circ_225467,RMVar_hsa_circ_225472,RMVar_hsa_circ_271227,RMVar_hsa_circ_225471,RMVar_hsa_circ_225476,RMVar_hsa_circ_225474,RMVar_hsa_circ_287533,RMVar_hsa_circ_313227,RMVar_hsa_circ_225473,RMVar_hsa_circ_225477,RMVar_hsa_circ_279938,RMVar_hsa_circ_280268,RMVar_hsa_circ_225478 3040 RMVar_ID_3040 Human_SNP_ID_180854186 A-to-I Human chr4 + 39760056 39760056 39760056 AAATTAGCCAGGCGTGGGTGGTGGGCACCTGTAATCCCAGCTACTCGTGGGGCTGAGACAGGAGA AAATTAGCCAGGCGTGGGTGGTGGGCACCTGTTATCCCAGCTACTCGTGGGGCTGAGACAGGAGA A T UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1320462960 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_225460,RMVar_hsa_circ_225465,RMVar_hsa_circ_225464,RMVar_hsa_circ_225459,RMVar_hsa_circ_225463,RMVar_hsa_circ_225468,RMVar_hsa_circ_298369,RMVar_hsa_circ_225467,RMVar_hsa_circ_225472,RMVar_hsa_circ_271227,RMVar_hsa_circ_225471,RMVar_hsa_circ_225476,RMVar_hsa_circ_225474,RMVar_hsa_circ_287533,RMVar_hsa_circ_313227,RMVar_hsa_circ_225473,RMVar_hsa_circ_225477,RMVar_hsa_circ_279938,RMVar_hsa_circ_280268,RMVar_hsa_circ_225478 3041 RMVar_ID_3041 Human_SNP_ID_180855314 A-to-I Human chr4 + 39763879 39763879 39763879 TTCCCACCTCAGCCTTCTGAGTAACTGTAACTACAGTCACGTGCTACCACACTTGGCTAATTTTT TTCCCACCTCAGCCTTCTGAGTAACTGTAACTGCAGTCACGTGCTACCACACTTGGCTAATTTTT A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1296467927 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_225460,RMVar_hsa_circ_225465,RMVar_hsa_circ_225464,RMVar_hsa_circ_225459,RMVar_hsa_circ_225463,RMVar_hsa_circ_225468,RMVar_hsa_circ_298369,RMVar_hsa_circ_225467,RMVar_hsa_circ_225472,RMVar_hsa_circ_271227,RMVar_hsa_circ_225471,RMVar_hsa_circ_225476,RMVar_hsa_circ_225474,RMVar_hsa_circ_287533,RMVar_hsa_circ_313227,RMVar_hsa_circ_225473,RMVar_hsa_circ_225477,RMVar_hsa_circ_279938,RMVar_hsa_circ_280268,RMVar_hsa_circ_225478 3042 RMVar_ID_3042 Human_SNP_ID_180855327 A-to-I Human chr4 + 39763934 39763934 39763934 GCTAATTTTTTGTAGAGACAGAGTTTCACCTCATTGCCCAGGCTGGTCTTAAACTCCTGGGCTCA GCTAATTTTTTGTAGAGACAGAGTTTCACCTCGTTGCCCAGGCTGGTCTTAAACTCCTGGGCTCA A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs954724596 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_225460,RMVar_hsa_circ_225465,RMVar_hsa_circ_225464,RMVar_hsa_circ_225459,RMVar_hsa_circ_225463,RMVar_hsa_circ_225468,RMVar_hsa_circ_298369,RMVar_hsa_circ_225467,RMVar_hsa_circ_225472,RMVar_hsa_circ_271227,RMVar_hsa_circ_225471,RMVar_hsa_circ_225476,RMVar_hsa_circ_225474,RMVar_hsa_circ_287533,RMVar_hsa_circ_313227,RMVar_hsa_circ_225473,RMVar_hsa_circ_225477,RMVar_hsa_circ_279938,RMVar_hsa_circ_280268,RMVar_hsa_circ_225478 3043 RMVar_ID_3043 Human_SNP_ID_180855386 A-to-I Human chr4 + 39764216 39764216 39764216 GTCTGTACAAAAAATTTTAAAATTAGCTGGGCATGGTGTTGCGTGCCTGTAGTCTAAGGTGAGAA GTCTGTACAAAAAATTTTAAAATTAGCTGGGCGTGGTGTTGCGTGCCTGTAGTCTAAGGTGAGAA A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1361651521 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17574615 RMVar_hsa_circ_225460,RMVar_hsa_circ_225465,RMVar_hsa_circ_225464,RMVar_hsa_circ_225459,RMVar_hsa_circ_225463,RMVar_hsa_circ_225468,RMVar_hsa_circ_298369,RMVar_hsa_circ_225467,RMVar_hsa_circ_225472,RMVar_hsa_circ_271227,RMVar_hsa_circ_225471,RMVar_hsa_circ_225476,RMVar_hsa_circ_225474,RMVar_hsa_circ_287533,RMVar_hsa_circ_313227,RMVar_hsa_circ_225473,RMVar_hsa_circ_225477,RMVar_hsa_circ_279938,RMVar_hsa_circ_280268,RMVar_hsa_circ_225478 3044 RMVar_ID_3044 Human_SNP_ID_180855510 A-to-I Human chr4 + 39764702 39764702 39764702 CCCCTGTTTTGACTTCCCAAAGTGCTAGGATTATAGGCATGAGCCACTGCCCCCGGCTGATTTCT CCCCTGTTTTGACTTCCCAAAGTGCTAGGATTGTAGGCATGAGCCACTGCCCCCGGCTGATTTCT A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474286642 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25834480 RMVar_hsa_circ_225460,RMVar_hsa_circ_225465,RMVar_hsa_circ_225464,RMVar_hsa_circ_225459,RMVar_hsa_circ_225463,RMVar_hsa_circ_225468,RMVar_hsa_circ_298369,RMVar_hsa_circ_225467,RMVar_hsa_circ_225472,RMVar_hsa_circ_271227,RMVar_hsa_circ_225471,RMVar_hsa_circ_225476,RMVar_hsa_circ_225474,RMVar_hsa_circ_287533,RMVar_hsa_circ_313227,RMVar_hsa_circ_225473,RMVar_hsa_circ_225477,RMVar_hsa_circ_279938,RMVar_hsa_circ_280268,RMVar_hsa_circ_225478 3045 RMVar_ID_3045 Human_SNP_ID_180855684 A-to-I Human chr4 + 39765322 39765322 39765322 AAGGTGGGTGGATCGCTTGAGCCCAGGAGTTCAAGACCAGCCTGGGCAACATGGTGAAACTCCAT AAGGTGGGTGGATCGCTTGAGCCCAGGAGTTCCAGACCAGCCTGGGCAACATGGTGAAACTCCAT A C UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs972856030 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_225460,RMVar_hsa_circ_225465,RMVar_hsa_circ_225464,RMVar_hsa_circ_225459,RMVar_hsa_circ_225463,RMVar_hsa_circ_225468,RMVar_hsa_circ_298369,RMVar_hsa_circ_225467,RMVar_hsa_circ_225472,RMVar_hsa_circ_271227,RMVar_hsa_circ_225471,RMVar_hsa_circ_225476,RMVar_hsa_circ_225474,RMVar_hsa_circ_287533,RMVar_hsa_circ_313227,RMVar_hsa_circ_225473,RMVar_hsa_circ_225477,RMVar_hsa_circ_279938,RMVar_hsa_circ_280268,RMVar_hsa_circ_225478 3046 RMVar_ID_3046 Human_SNP_ID_180855685 A-to-I Human chr4 + 39765322 39765322 39765322 AAGGTGGGTGGATCGCTTGAGCCCAGGAGTTCAAGACCAGCCTGGGCAACATGGTGAAACTCCAT AAGGTGGGTGGATCGCTTGAGCCCAGGAGTTCGAGACCAGCCTGGGCAACATGGTGAAACTCCAT A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs972856030 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_225460,RMVar_hsa_circ_225465,RMVar_hsa_circ_225464,RMVar_hsa_circ_225459,RMVar_hsa_circ_225463,RMVar_hsa_circ_225468,RMVar_hsa_circ_298369,RMVar_hsa_circ_225467,RMVar_hsa_circ_225472,RMVar_hsa_circ_271227,RMVar_hsa_circ_225471,RMVar_hsa_circ_225476,RMVar_hsa_circ_225474,RMVar_hsa_circ_287533,RMVar_hsa_circ_313227,RMVar_hsa_circ_225473,RMVar_hsa_circ_225477,RMVar_hsa_circ_279938,RMVar_hsa_circ_280268,RMVar_hsa_circ_225478 3047 RMVar_ID_3047 Human_SNP_ID_180855795 A-to-I Human chr4 + 39765741 39765741 39765741 CTACTAGGGAGAATCGCTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCCAAGATTGTGCCACTGC CTACTAGGGAGAATCGCTTGAACCTGGGAGGCGGAGGTTGCAGTGAGCCAAGATTGTGCCACTGC A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs934442109 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_225460,RMVar_hsa_circ_225465,RMVar_hsa_circ_225464,RMVar_hsa_circ_225459,RMVar_hsa_circ_225463,RMVar_hsa_circ_225468,RMVar_hsa_circ_298369,RMVar_hsa_circ_225467,RMVar_hsa_circ_225472,RMVar_hsa_circ_271227,RMVar_hsa_circ_225471,RMVar_hsa_circ_225476,RMVar_hsa_circ_225474,RMVar_hsa_circ_287533,RMVar_hsa_circ_313227,RMVar_hsa_circ_225473,RMVar_hsa_circ_225477,RMVar_hsa_circ_279938,RMVar_hsa_circ_280268,RMVar_hsa_circ_225478 3048 RMVar_ID_3048 Human_SNP_ID_180856314 A-to-I Human chr4 + 39767441 39767441 39767441 TGCCTCCCGGATTCACGCCATTCTCCTGCCTCAGCCTCCAGAGTAGCTGGGACTACAGGCGCCTG TGCCTCCCGGATTCACGCCATTCTCCTGCCTCGGCCTCCAGAGTAGCTGGGACTACAGGCGCCTG A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1361826612 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_225460,RMVar_hsa_circ_225465,RMVar_hsa_circ_225464,RMVar_hsa_circ_225459,RMVar_hsa_circ_225463,RMVar_hsa_circ_225468,RMVar_hsa_circ_298369,RMVar_hsa_circ_225467,RMVar_hsa_circ_225472,RMVar_hsa_circ_271227,RMVar_hsa_circ_225471,RMVar_hsa_circ_225476,RMVar_hsa_circ_225474,RMVar_hsa_circ_287533,RMVar_hsa_circ_313227,RMVar_hsa_circ_225473,RMVar_hsa_circ_225477,RMVar_hsa_circ_279938,RMVar_hsa_circ_280268,RMVar_hsa_circ_225478 3049 RMVar_ID_3049 Human_SNP_ID_180856356 A-to-I Human chr4 + 39767597 39767597 39767597 CACCCACCTCGGCCTCCCAAAGTGTTGGGATTACAGGCATGAGCCACTGCGCCCGGCCCAGGATT CACCCACCTCGGCCTCCCAAAGTGTTGGGATTGCAGGCATGAGCCACTGCGCCCGGCCCAGGATT A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1387982150 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15149546,Human_RBP_ID_25809921 RMVar_hsa_circ_225460,RMVar_hsa_circ_225465,RMVar_hsa_circ_225464,RMVar_hsa_circ_225459,RMVar_hsa_circ_225463,RMVar_hsa_circ_225468,RMVar_hsa_circ_298369,RMVar_hsa_circ_225467,RMVar_hsa_circ_225472,RMVar_hsa_circ_271227,RMVar_hsa_circ_225471,RMVar_hsa_circ_225476,RMVar_hsa_circ_225474,RMVar_hsa_circ_287533,RMVar_hsa_circ_313227,RMVar_hsa_circ_225473,RMVar_hsa_circ_225477,RMVar_hsa_circ_279938,RMVar_hsa_circ_280268,RMVar_hsa_circ_225478 3050 RMVar_ID_3050 Human_SNP_ID_180856746 A-to-I Human chr4 + 39769006 39769006 39769006 CACTATCACGGCCAGAAAATTTTTGTGTATTTAGTAGAGATGGGGTTTCGCCATGTTGCCCAGGT CACTATCACGGCCAGAAAATTTTTGTGTATTTGGTAGAGATGGGGTTTCGCCATGTTGCCCAGGT A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1388035560 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15149578 RMVar_hsa_circ_225460,RMVar_hsa_circ_225465,RMVar_hsa_circ_225464,RMVar_hsa_circ_225459,RMVar_hsa_circ_225463,RMVar_hsa_circ_225468,RMVar_hsa_circ_298369,RMVar_hsa_circ_225467,RMVar_hsa_circ_225472,RMVar_hsa_circ_271227,RMVar_hsa_circ_225471,RMVar_hsa_circ_225476,RMVar_hsa_circ_225474,RMVar_hsa_circ_287533,RMVar_hsa_circ_313227,RMVar_hsa_circ_225473,RMVar_hsa_circ_225477,RMVar_hsa_circ_279938,RMVar_hsa_circ_280268,RMVar_hsa_circ_225478 3051 RMVar_ID_3051 Human_SNP_ID_180857757 A-to-I Human chr4 + 39771918 39771918 39771918 GCTGGAGTGCGGTGGCGCCATCTGGACTCACTATAACCTTCGCCTCCCAGGTTCGAGCGATTCCT GCTGGAGTGCGGTGGCGCCATCTGGACTCACTGTAACCTTCGCCTCCCAGGTTCGAGCGATTCCT A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1374528750 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25809944 RMVar_hsa_circ_225460,RMVar_hsa_circ_225465,RMVar_hsa_circ_225464,RMVar_hsa_circ_225459,RMVar_hsa_circ_225463,RMVar_hsa_circ_225468,RMVar_hsa_circ_298369,RMVar_hsa_circ_225467,RMVar_hsa_circ_225472,RMVar_hsa_circ_271227,RMVar_hsa_circ_225471,RMVar_hsa_circ_225476,RMVar_hsa_circ_225474,RMVar_hsa_circ_287533,RMVar_hsa_circ_313227,RMVar_hsa_circ_225473,RMVar_hsa_circ_225477,RMVar_hsa_circ_279938,RMVar_hsa_circ_280268,RMVar_hsa_circ_225478 3052 RMVar_ID_3052 Human_SNP_ID_180857763 A-to-I Human chr4 + 39771934 39771934 39771934 GCCATCTGGACTCACTATAACCTTCGCCTCCCAGGTTCGAGCGATTCCTGCCTCAGCCCCTCAAG GCCATCTGGACTCACTATAACCTTCGCCTCCCGGGTTCGAGCGATTCCTGCCTCAGCCCCTCAAG A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1446252716 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_225460,RMVar_hsa_circ_225465,RMVar_hsa_circ_225464,RMVar_hsa_circ_225459,RMVar_hsa_circ_225463,RMVar_hsa_circ_225468,RMVar_hsa_circ_298369,RMVar_hsa_circ_225467,RMVar_hsa_circ_225472,RMVar_hsa_circ_271227,RMVar_hsa_circ_225471,RMVar_hsa_circ_225476,RMVar_hsa_circ_225474,RMVar_hsa_circ_287533,RMVar_hsa_circ_313227,RMVar_hsa_circ_225473,RMVar_hsa_circ_225477,RMVar_hsa_circ_279938,RMVar_hsa_circ_280268,RMVar_hsa_circ_225478 3053 RMVar_ID_3053 Human_SNP_ID_180857784 A-to-I Human chr4 + 39772026 39772026 39772026 ACATCTGGCTAATTTTTGTATTTTTGGCAGACAGTGTTTCGCCATGTTGCCCAGGCTGGTCTCAA ACATCTGGCTAATTTTTGTATTTTTGGCAGACGGTGTTTCGCCATGTTGCCCAGGCTGGTCTCAA A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1358714815 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_225460,RMVar_hsa_circ_225465,RMVar_hsa_circ_225464,RMVar_hsa_circ_225459,RMVar_hsa_circ_225463,RMVar_hsa_circ_225468,RMVar_hsa_circ_298369,RMVar_hsa_circ_225467,RMVar_hsa_circ_225472,RMVar_hsa_circ_271227,RMVar_hsa_circ_225471,RMVar_hsa_circ_225476,RMVar_hsa_circ_225474,RMVar_hsa_circ_287533,RMVar_hsa_circ_313227,RMVar_hsa_circ_225473,RMVar_hsa_circ_225477,RMVar_hsa_circ_279938,RMVar_hsa_circ_280268,RMVar_hsa_circ_225478 3054 RMVar_ID_3054 Human_SNP_ID_180858206 A-to-I Human chr4 + 39773329 39773329 39773329 GTTCTACTAAAACTACAAAAAATTAGCCGGGCATGGTGGCATGTGCCTGTAGTCCCAGCTACTTG GTTCTACTAAAACTACAAAAAATTAGCCGGGCGTGGTGGCATGTGCCTGTAGTCCCAGCTACTTG A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1192685761 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_225460,RMVar_hsa_circ_225465,RMVar_hsa_circ_225464,RMVar_hsa_circ_225459,RMVar_hsa_circ_225463,RMVar_hsa_circ_225468,RMVar_hsa_circ_298369,RMVar_hsa_circ_225467,RMVar_hsa_circ_225472,RMVar_hsa_circ_271227,RMVar_hsa_circ_225471,RMVar_hsa_circ_225476,RMVar_hsa_circ_225474,RMVar_hsa_circ_287533,RMVar_hsa_circ_313227,RMVar_hsa_circ_225473,RMVar_hsa_circ_225477,RMVar_hsa_circ_279938,RMVar_hsa_circ_280268,RMVar_hsa_circ_225478 3055 RMVar_ID_3055 Human_SNP_ID_180858216 A-to-I Human chr4 + 39773347 39773347 39773347 AAAATTAGCCGGGCATGGTGGCATGTGCCTGTAGTCCCAGCTACTTGTGAGGCTGAGGCAGGAGA AAAATTAGCCGGGCATGGTGGCATGTGCCTGTTGTCCCAGCTACTTGTGAGGCTGAGGCAGGAGA A T UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs182254567 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_225460,RMVar_hsa_circ_225465,RMVar_hsa_circ_225464,RMVar_hsa_circ_225459,RMVar_hsa_circ_225463,RMVar_hsa_circ_225468,RMVar_hsa_circ_298369,RMVar_hsa_circ_225467,RMVar_hsa_circ_225472,RMVar_hsa_circ_271227,RMVar_hsa_circ_225471,RMVar_hsa_circ_225476,RMVar_hsa_circ_225474,RMVar_hsa_circ_287533,RMVar_hsa_circ_313227,RMVar_hsa_circ_225473,RMVar_hsa_circ_225477,RMVar_hsa_circ_279938,RMVar_hsa_circ_280268,RMVar_hsa_circ_225478 3056 RMVar_ID_3056 Human_SNP_ID_180858502 A-to-I Human chr4 + 39774029 39774029 39774029 CTTAAGAAATAGAAAAGCTGGCCGAGTGTAGTAGCTCACACCTGTAACCCTAACCTTTGGGAGGC CTTAAGAAATAGAAAAGCTGGCCGAGTGTAGTGGCTCACACCTGTAACCCTAACCTTTGGGAGGC A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1012331011 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15149657 RMVar_hsa_circ_225460,RMVar_hsa_circ_225465,RMVar_hsa_circ_225464,RMVar_hsa_circ_225459,RMVar_hsa_circ_225463,RMVar_hsa_circ_225468,RMVar_hsa_circ_298369,RMVar_hsa_circ_225467,RMVar_hsa_circ_225472,RMVar_hsa_circ_271227,RMVar_hsa_circ_225471,RMVar_hsa_circ_225476,RMVar_hsa_circ_225474,RMVar_hsa_circ_287533,RMVar_hsa_circ_313227,RMVar_hsa_circ_225473,RMVar_hsa_circ_225477,RMVar_hsa_circ_279938,RMVar_hsa_circ_280268,RMVar_hsa_circ_225478 3057 RMVar_ID_3057 Human_SNP_ID_180858559 A-to-I Human chr4 + 39774183 39774183 39774183 AAAAAATGCTGGGTGTGGTGGTGTGTGCCTGTAGTCCCAGCTACTCGTGAGGCTGAGGCAGGAGA AAAAAATGCTGGGTGTGGTGGTGTGTGCCTGTTGTCCCAGCTACTCGTGAGGCTGAGGCAGGAGA A T UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1307793579 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_225460,RMVar_hsa_circ_225465,RMVar_hsa_circ_225464,RMVar_hsa_circ_225459,RMVar_hsa_circ_225463,RMVar_hsa_circ_225468,RMVar_hsa_circ_298369,RMVar_hsa_circ_225467,RMVar_hsa_circ_225472,RMVar_hsa_circ_271227,RMVar_hsa_circ_225471,RMVar_hsa_circ_225476,RMVar_hsa_circ_225474,RMVar_hsa_circ_287533,RMVar_hsa_circ_313227,RMVar_hsa_circ_225473,RMVar_hsa_circ_225477,RMVar_hsa_circ_279938,RMVar_hsa_circ_280268,RMVar_hsa_circ_225478 3058 RMVar_ID_3058 Human_SNP_ID_180875437 A-to-I Human chr4 - 39829469 39829469 39829469 TAATTTTTGTGTTTTTGTAGAGATGAGGTTTCACCATATTGGTCAGGCTGGTCCTGATCTCCTGA TAATTTTTGTGTTTTTGTAGAGATGAGGTTTCGCCATATTGGTCAGGCTGGTCCTGATCTCCTGA T C PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1229599960 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96208,RMVar_hsa_circ_118437,RMVar_hsa_circ_127708,RMVar_hsa_circ_268799,RMVar_hsa_circ_120167,RMVar_hsa_circ_117569,RMVar_hsa_circ_225482,RMVar_hsa_circ_225484,RMVar_hsa_circ_225486,RMVar_hsa_circ_85409,RMVar_hsa_circ_225487,RMVar_hsa_circ_225485,RMVar_hsa_circ_225483 3059 RMVar_ID_3059 Human_SNP_ID_180875559 A-to-I Human chr4 - 39829793 39829793 39829793 GCACCCACCACCACGCCCGGCTAATTTTTTGTATTTTTAGTGGAGACAGGGTTTCACCGTGTTAG GCACCCACCACCACGCCCGGCTAATTTTTTGTGTTTTTAGTGGAGACAGGGTTTCACCGTGTTAG T C PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1403563162 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96208,RMVar_hsa_circ_118437,RMVar_hsa_circ_127708,RMVar_hsa_circ_268799,RMVar_hsa_circ_120167,RMVar_hsa_circ_117569,RMVar_hsa_circ_225482,RMVar_hsa_circ_225484,RMVar_hsa_circ_225486,RMVar_hsa_circ_85409,RMVar_hsa_circ_225487,RMVar_hsa_circ_225485,RMVar_hsa_circ_225483 3060 RMVar_ID_3060 Human_SNP_ID_180875804 A-to-I Human chr4 - 39830492 39830492 39830492 AAACCTGGGAGGTTGGAGGTTGCAGTGAGCCAAGATCTTGCCAGTGCACTCCATCCTGGGCAACA AAACCTGGGAGGTTGGAGGTTGCAGTGAGCCAGGATCTTGCCAGTGCACTCCATCCTGGGCAACA T C PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1307940752 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96208,RMVar_hsa_circ_118437,RMVar_hsa_circ_127708,RMVar_hsa_circ_268799,RMVar_hsa_circ_120167,RMVar_hsa_circ_117569,RMVar_hsa_circ_225482,RMVar_hsa_circ_225484,RMVar_hsa_circ_225486,RMVar_hsa_circ_85409,RMVar_hsa_circ_225487,RMVar_hsa_circ_225485,RMVar_hsa_circ_225483 3061 RMVar_ID_3061 Human_SNP_ID_180875962 A-to-I Human chr4 - 39831165 39831165 39831165 GGAGGCAATTGAACTTGGGAGGCGGAGGTTGCAGTGAACCAAGATCACACCATGCACTCCAGCCT GGAGGCAATTGAACTTGGGAGGCGGAGGTTGCGGTGAACCAAGATCACACCATGCACTCCAGCCT T C PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1247765386 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10148179 RMVar_hsa_circ_96208,RMVar_hsa_circ_118437,RMVar_hsa_circ_127708,RMVar_hsa_circ_268799,RMVar_hsa_circ_120167,RMVar_hsa_circ_117569,RMVar_hsa_circ_225482,RMVar_hsa_circ_225484,RMVar_hsa_circ_225486,RMVar_hsa_circ_85409,RMVar_hsa_circ_225487,RMVar_hsa_circ_225485,RMVar_hsa_circ_225483 3062 RMVar_ID_3062 Human_SNP_ID_180875980 A-to-I Human chr4 - 39831237 39831237 39831237 ATTTAGCCGGGCATGGTGGCGCACGCGCCTCTAGTCCCAGCTACTCAGTAGGCTGAGGCAGAAGA ATTTAGCCGGGCATGGTGGCGCACGCGCCTCTGGTCCCAGCTACTCAGTAGGCTGAGGCAGAAGA T C PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1224235299 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96208,RMVar_hsa_circ_118437,RMVar_hsa_circ_127708,RMVar_hsa_circ_268799,RMVar_hsa_circ_120167,RMVar_hsa_circ_117569,RMVar_hsa_circ_225482,RMVar_hsa_circ_225484,RMVar_hsa_circ_225486,RMVar_hsa_circ_85409,RMVar_hsa_circ_225487,RMVar_hsa_circ_225485,RMVar_hsa_circ_225483 3063 RMVar_ID_3063 Human_SNP_ID_180876111 A-to-I Human chr4 - 39831790 39831790 39831790 CTCACCGCAACCTCCGCCTTCCAGTCCAAGCAATTCTCCTGCCTCAGCCTCCCTAGTAGCTGGGA CTCACCGCAACCTCCGCCTTCCAGTCCAAGCAGTTCTCCTGCCTCAGCCTCCCTAGTAGCTGGGA T C PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1477096940 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96208,RMVar_hsa_circ_118437,RMVar_hsa_circ_127708,RMVar_hsa_circ_268799,RMVar_hsa_circ_120167,RMVar_hsa_circ_117569,RMVar_hsa_circ_225482,RMVar_hsa_circ_225484,RMVar_hsa_circ_225486,RMVar_hsa_circ_85409,RMVar_hsa_circ_225487,RMVar_hsa_circ_225485,RMVar_hsa_circ_225483 3064 RMVar_ID_3064 Human_SNP_ID_180876112 A-to-I Human chr4 - 39831794 39831794 39831794 TCGGCTCACCGCAACCTCCGCCTTCCAGTCCAAGCAATTCTCCTGCCTCAGCCTCCCTAGTAGCT TCGGCTCACCGCAACCTCCGCCTTCCAGTCCAGGCAATTCTCCTGCCTCAGCCTCCCTAGTAGCT T C PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1357181230 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96208,RMVar_hsa_circ_118437,RMVar_hsa_circ_127708,RMVar_hsa_circ_268799,RMVar_hsa_circ_120167,RMVar_hsa_circ_117569,RMVar_hsa_circ_225482,RMVar_hsa_circ_225484,RMVar_hsa_circ_225486,RMVar_hsa_circ_85409,RMVar_hsa_circ_225487,RMVar_hsa_circ_225485,RMVar_hsa_circ_225483 3065 RMVar_ID_3065 Human_SNP_ID_180876203 A-to-I Human chr4 - 39831957 39831957 39831957 GATGTGCGCCACCACACCCGGCTAATTTTTGTATTTGTAGTAGAGACGGGTTTCACCGTGTTGGG GATGTGCGCCACCACACCCGGCTAATTTTTGTTTTTGTAGTAGAGACGGGTTTCACCGTGTTGGG T A PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs867234473 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96208,RMVar_hsa_circ_118437,RMVar_hsa_circ_127708,RMVar_hsa_circ_268799,RMVar_hsa_circ_120167,RMVar_hsa_circ_117569,RMVar_hsa_circ_225482,RMVar_hsa_circ_225484,RMVar_hsa_circ_225486,RMVar_hsa_circ_85409,RMVar_hsa_circ_225487,RMVar_hsa_circ_225485,RMVar_hsa_circ_225483 3066 RMVar_ID_3066 Human_SNP_ID_180876204 A-to-I Human chr4 - 39831957 39831957 39831957 GATGTGCGCCACCACACCCGGCTAATTTTTGTATTTGTAGTAGAGACGGGTTTCACCGTGTTGGG GATGTGCGCCACCACACCCGGCTAATTTTTGTGTTTGTAGTAGAGACGGGTTTCACCGTGTTGGG T C PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs867234473 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96208,RMVar_hsa_circ_118437,RMVar_hsa_circ_127708,RMVar_hsa_circ_268799,RMVar_hsa_circ_120167,RMVar_hsa_circ_117569,RMVar_hsa_circ_225482,RMVar_hsa_circ_225484,RMVar_hsa_circ_225486,RMVar_hsa_circ_85409,RMVar_hsa_circ_225487,RMVar_hsa_circ_225485,RMVar_hsa_circ_225483 3067 RMVar_ID_3067 Human_SNP_ID_180876205 A-to-I Human chr4 - 39831966 39831966 39831966 GGGACTGCAGATGTGCGCCACCACACCCGGCTAATTTTTGTATTTGTAGTAGAGACGGGTTTCAC GGGACTGCAGATGTGCGCCACCACACCCGGCTCATTTTTGTATTTGTAGTAGAGACGGGTTTCAC T G PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1184552573 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96208,RMVar_hsa_circ_118437,RMVar_hsa_circ_127708,RMVar_hsa_circ_268799,RMVar_hsa_circ_120167,RMVar_hsa_circ_117569,RMVar_hsa_circ_225482,RMVar_hsa_circ_225484,RMVar_hsa_circ_225486,RMVar_hsa_circ_85409,RMVar_hsa_circ_225487,RMVar_hsa_circ_225485,RMVar_hsa_circ_225483 3068 RMVar_ID_3068 Human_SNP_ID_180876240 A-to-I Human chr4 - 39832079 39832079 39832079 GAGTCTTGCTCTGTCACCCAGGCTGGAGTACAATGGTGAGATCTCGGCTCACTGCACCCTCTGCC GAGTCTTGCTCTGTCACCCAGGCTGGAGTACAGTGGTGAGATCTCGGCTCACTGCACCCTCTGCC T C PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs940871079 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15150245 RMVar_hsa_circ_96208,RMVar_hsa_circ_118437,RMVar_hsa_circ_127708,RMVar_hsa_circ_268799,RMVar_hsa_circ_120167,RMVar_hsa_circ_117569,RMVar_hsa_circ_225482,RMVar_hsa_circ_225484,RMVar_hsa_circ_225486,RMVar_hsa_circ_85409,RMVar_hsa_circ_225487,RMVar_hsa_circ_225485,RMVar_hsa_circ_225483 3069 RMVar_ID_3069 Human_SNP_ID_180876299 A-to-I Human chr4 - 39832290 39832290 39832290 AGAATGGCATGAACCCAGGGGGCGGAGCTTGCAGTGAGCAGAGATCACACCACTGCACTCCAGCC AGAATGGCATGAACCCAGGGGGCGGAGCTTGCCGTGAGCAGAGATCACACCACTGCACTCCAGCC T G PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs921819453 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96208,RMVar_hsa_circ_118437,RMVar_hsa_circ_127708,RMVar_hsa_circ_268799,RMVar_hsa_circ_120167,RMVar_hsa_circ_117569,RMVar_hsa_circ_225482,RMVar_hsa_circ_225484,RMVar_hsa_circ_225486,RMVar_hsa_circ_85409,RMVar_hsa_circ_225487,RMVar_hsa_circ_225485,RMVar_hsa_circ_225483 3070 RMVar_ID_3070 Human_SNP_ID_180876348 A-to-I Human chr4 - 39832482 39832482 39832482 AAATTTTGAGCCAGGAACGGTGGCTCATGCCTATAATCTCAGCACTTTGGGAGGCGGGTGGATCA AAATTTTGAGCCAGGAACGGTGGCTCATGCCTGTAATCTCAGCACTTTGGGAGGCGGGTGGATCA T C PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1379625650 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96208,RMVar_hsa_circ_118437,RMVar_hsa_circ_127708,RMVar_hsa_circ_268799,RMVar_hsa_circ_120167,RMVar_hsa_circ_117569,RMVar_hsa_circ_225482,RMVar_hsa_circ_225484,RMVar_hsa_circ_225486,RMVar_hsa_circ_85409,RMVar_hsa_circ_225487,RMVar_hsa_circ_225485,RMVar_hsa_circ_225483 3071 RMVar_ID_3071 Human_SNP_ID_180876424 A-to-I Human chr4 - 39832768 39832768 39832768 CTTTGTTCTATGAGAGCACTGAGGCTCAAGCAATCCTCTTGCCTCAGCCTCCCAAGTAGCTGGGA CTTTGTTCTATGAGAGCACTGAGGCTCAAGCAGTCCTCTTGCCTCAGCCTCCCAAGTAGCTGGGA T C PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1169277642 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96208,RMVar_hsa_circ_118437,RMVar_hsa_circ_127708,RMVar_hsa_circ_268799,RMVar_hsa_circ_120167,RMVar_hsa_circ_117569,RMVar_hsa_circ_225482,RMVar_hsa_circ_225484,RMVar_hsa_circ_225486,RMVar_hsa_circ_85409,RMVar_hsa_circ_225487,RMVar_hsa_circ_225485,RMVar_hsa_circ_225483 3072 RMVar_ID_3072 Human_SNP_ID_180876436 A-to-I Human chr4 - 39832832 39832832 39832832 TTTTTTGAGAGACCAGTCTCACTCTGTCACTCAGGCTGGAGTGCAGTGGCACCATCATGGCTCAC TTTTTTGAGAGACCAGTCTCACTCTGTCACTCGGGCTGGAGTGCAGTGGCACCATCATGGCTCAC T C PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1205813778 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23190965 RMVar_hsa_circ_96208,RMVar_hsa_circ_118437,RMVar_hsa_circ_127708,RMVar_hsa_circ_268799,RMVar_hsa_circ_120167,RMVar_hsa_circ_117569,RMVar_hsa_circ_225482,RMVar_hsa_circ_225484,RMVar_hsa_circ_225486,RMVar_hsa_circ_85409,RMVar_hsa_circ_225487,RMVar_hsa_circ_225485,RMVar_hsa_circ_225483 3073 RMVar_ID_3073 Human_SNP_ID_180876638 A-to-I Human chr4 - 39833467 39833467 39833467 AGGGGATCACCTGAGCCTGGGAGGTCGAGGCTACAGTGAGTCATGATCATGCCACTCCTCACTGC AGGGGATCACCTGAGCCTGGGAGGTCGAGGCTGCAGTGAGTCATGATCATGCCACTCCTCACTGC T C PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1399778117 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7309589 RMVar_hsa_circ_96208,RMVar_hsa_circ_118437,RMVar_hsa_circ_127708,RMVar_hsa_circ_268799,RMVar_hsa_circ_120167,RMVar_hsa_circ_117569,RMVar_hsa_circ_225482,RMVar_hsa_circ_225484,RMVar_hsa_circ_225486,RMVar_hsa_circ_85409,RMVar_hsa_circ_225487,RMVar_hsa_circ_225485,RMVar_hsa_circ_225483 3074 RMVar_ID_3074 Human_SNP_ID_180876653 A-to-I Human chr4 - 39833529 39833529 39833529 AGAAAAATTAGCCAGGTGTCTGGTATGTGCCCATAGTCTTGGCTACTTCAGAGGCTGAGGTGAGG AGAAAAATTAGCCAGGTGTCTGGTATGTGCCCGTAGTCTTGGCTACTTCAGAGGCTGAGGTGAGG T C PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1450916679 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18824027 RMVar_hsa_circ_96208,RMVar_hsa_circ_118437,RMVar_hsa_circ_127708,RMVar_hsa_circ_268799,RMVar_hsa_circ_120167,RMVar_hsa_circ_117569,RMVar_hsa_circ_225482,RMVar_hsa_circ_225484,RMVar_hsa_circ_225486,RMVar_hsa_circ_85409,RMVar_hsa_circ_225487,RMVar_hsa_circ_225485,RMVar_hsa_circ_225483 3075 RMVar_ID_3075 Human_SNP_ID_180877124 A-to-I Human chr4 - 39835651 39835651 39835651 GGGCTTGGTGGTGCACACCTGTAGTGCCAGCTACTCGCGAGACTGAGGCAGGAGAATTGCTTGAA GGGCTTGGTGGTGCACACCTGTAGTGCCAGCTGCTCGCGAGACTGAGGCAGGAGAATTGCTTGAA T C PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1358843002 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8591357,Human_RBP_ID_15150316 RMVar_hsa_circ_96208,RMVar_hsa_circ_118437,RMVar_hsa_circ_127708,RMVar_hsa_circ_268799,RMVar_hsa_circ_120167,RMVar_hsa_circ_117569,RMVar_hsa_circ_225482,RMVar_hsa_circ_225484,RMVar_hsa_circ_225486,RMVar_hsa_circ_85409,RMVar_hsa_circ_225487,RMVar_hsa_circ_225485,RMVar_hsa_circ_225483 3076 RMVar_ID_3076 Human_SNP_ID_180878657 A-to-I Human chr4 - 39840857 39840857 39840857 CCAGCTACTCAAGAGGTCGAGACAGGAGAATCACTTGAACCCTCGAGGTGAAGGTTGCAGTGAGC CCAGCTACTCAAGAGGTCGAGACAGGAGAATCGCTTGAACCCTCGAGGTGAAGGTTGCAGTGAGC T C PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs898797933 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96208,RMVar_hsa_circ_118437,RMVar_hsa_circ_127708,RMVar_hsa_circ_268799,RMVar_hsa_circ_120167,RMVar_hsa_circ_117569,RMVar_hsa_circ_30984,RMVar_hsa_circ_225482,RMVar_hsa_circ_225484,RMVar_hsa_circ_225486,RMVar_hsa_circ_85409,RMVar_hsa_circ_225487,RMVar_hsa_circ_225485,RMVar_hsa_circ_225483,RMVar_hsa_circ_225490,RMVar_hsa_circ_288401,RMVar_hsa_circ_328364,RMVar_hsa_circ_343723,RMVar_hsa_circ_346881,RMVar_hsa_circ_355929,RMVar_hsa_circ_343380,RMVar_hsa_circ_313169,RMVar_hsa_circ_51052,RMVar_hsa_circ_282549,RMVar_hsa_circ_31813,RMVar_hsa_circ_225491,RMVar_hsa_circ_225493,RMVar_hsa_circ_14446,RMVar_hsa_circ_225494,RMVar_hsa_circ_225492 3077 RMVar_ID_3077 Human_SNP_ID_180878675 A-to-I Human chr4 - 39840919 39840919 39840919 AAACCCCGTCTCTACTAAAAATACAAAATATTAGCCAGGCATGGTGGCGCACACCTGTAATCCCA AAACCCCGTCTCTACTAAAAATACAAAATATTCGCCAGGCATGGTGGCGCACACCTGTAATCCCA T G PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1252108005 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96208,RMVar_hsa_circ_118437,RMVar_hsa_circ_127708,RMVar_hsa_circ_268799,RMVar_hsa_circ_120167,RMVar_hsa_circ_117569,RMVar_hsa_circ_30984,RMVar_hsa_circ_225482,RMVar_hsa_circ_225484,RMVar_hsa_circ_225486,RMVar_hsa_circ_85409,RMVar_hsa_circ_225487,RMVar_hsa_circ_225485,RMVar_hsa_circ_225483,RMVar_hsa_circ_225490,RMVar_hsa_circ_288401,RMVar_hsa_circ_328364,RMVar_hsa_circ_343723,RMVar_hsa_circ_346881,RMVar_hsa_circ_355929,RMVar_hsa_circ_343380,RMVar_hsa_circ_313169,RMVar_hsa_circ_51052,RMVar_hsa_circ_282549,RMVar_hsa_circ_31813,RMVar_hsa_circ_225491,RMVar_hsa_circ_225493,RMVar_hsa_circ_14446,RMVar_hsa_circ_225494,RMVar_hsa_circ_225492 3078 RMVar_ID_3078 Human_SNP_ID_180891189 A-to-I Human chr4 - 39891937 39891937 39891937 CTGGCTAATTTTTTGTATTTTTTGGTAGAAACAGGGTTTTGCCATGTTTTCCAGACTGGTGTCAA CTGGCTAATTTTTTGTATTTTTTGGTAGAAACGGGGTTTTGCCATGTTTTCCAGACTGGTGTCAA T C PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1241014250 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118437,RMVar_hsa_circ_127708,RMVar_hsa_circ_120167,RMVar_hsa_circ_117569,RMVar_hsa_circ_30984,RMVar_hsa_circ_225482,RMVar_hsa_circ_225484,RMVar_hsa_circ_225486,RMVar_hsa_circ_85409,RMVar_hsa_circ_225485,RMVar_hsa_circ_225483,RMVar_hsa_circ_343723,RMVar_hsa_circ_355929,RMVar_hsa_circ_51052,RMVar_hsa_circ_99709,RMVar_hsa_circ_351817,RMVar_hsa_circ_225495,RMVar_hsa_circ_5131,RMVar_hsa_circ_726,RMVar_hsa_circ_22253,RMVar_hsa_circ_39688,RMVar_hsa_circ_225502,RMVar_hsa_circ_85345,RMVar_hsa_circ_80805,RMVar_hsa_circ_45042,RMVar_hsa_circ_225503,RMVar_hsa_circ_66244,RMVar_hsa_circ_225507,RMVar_hsa_circ_127738,RMVar_hsa_circ_225505,RMVar_hsa_circ_225504,RMVar_hsa_circ_45539,RMVar_hsa_circ_332594,RMVar_hsa_circ_41370,RMVar_hsa_circ_28222,RMVar_hsa_circ_30234,RMVar_hsa_circ_225510,RMVar_hsa_circ_225511,RMVar_hsa_circ_269628,RMVar_hsa_circ_89608,RMVar_hsa_circ_110839,RMVar_hsa_circ_225513,RMVar_hsa_circ_356874,RMVar_hsa_circ_225512,RMVar_hsa_circ_34344,RMVar_hsa_circ_225515,RMVar_hsa_circ_320638,RMVar_hsa_circ_351336,RMVar_hsa_circ_342706,RMVar_hsa_circ_296369,RMVar_hsa_circ_52835,RMVar_hsa_circ_25099,RMVar_hsa_circ_32771,RMVar_hsa_circ_68087,RMVar_hsa_circ_225516,RMVar_hsa_circ_225517,RMVar_hsa_circ_313124,RMVar_hsa_circ_345031,RMVar_hsa_circ_225523,RMVar_hsa_circ_340629,RMVar_hsa_circ_323243,RMVar_hsa_circ_316763,RMVar_hsa_circ_115099,RMVar_hsa_circ_117011,RMVar_hsa_circ_101014,RMVar_hsa_circ_43045,RMVar_hsa_circ_225526,RMVar_hsa_circ_225530,RMVar_hsa_circ_67338,RMVar_hsa_circ_20180,RMVar_hsa_circ_225528,RMVar_hsa_circ_225529,RMVar_hsa_circ_225527,RMVar_hsa_circ_225524,RMVar_hsa_circ_225525,RMVar_hsa_circ_353523,RMVar_hsa_circ_370364,RMVar_hsa_circ_309019,RMVar_hsa_circ_104888,RMVar_hsa_circ_52264,RMVar_hsa_circ_225535,RMVar_hsa_circ_225537,RMVar_hsa_circ_26094,RMVar_hsa_circ_225536,RMVar_hsa_circ_72227,RMVar_hsa_circ_6863,RMVar_hsa_circ_44268,RMVar_hsa_circ_8174,RMVar_hsa_circ_347851,RMVar_hsa_circ_225538,RMVar_hsa_circ_369150,RMVar_hsa_circ_372517,RMVar_hsa_circ_308361,RMVar_hsa_circ_352955,RMVar_hsa_circ_359849,RMVar_hsa_circ_371148,RMVar_hsa_circ_351920,RMVar_hsa_circ_35262,RMVar_hsa_circ_58738,RMVar_hsa_circ_11264,RMVar_hsa_circ_225541,RMVar_hsa_circ_225543,RMVar_hsa_circ_225544,RMVar_hsa_circ_225542,RMVar_hsa_circ_225540 3079 RMVar_ID_3079 Human_SNP_ID_180891746 A-to-I Human chr4 - 39894369 39894369 39894369 GGGTCTTGCTCTGTCACCCAGGCTGGAGTGTAATGACACAATCTCAGCTCACCGTAACCTCTGCA GGGTCTTGCTCTGTCACCCAGGCTGGAGTGTAGTGACACAATCTCAGCTCACCGTAACCTCTGCA T C PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1181463102 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118437,RMVar_hsa_circ_127708,RMVar_hsa_circ_120167,RMVar_hsa_circ_117569,RMVar_hsa_circ_30984,RMVar_hsa_circ_225482,RMVar_hsa_circ_225484,RMVar_hsa_circ_225486,RMVar_hsa_circ_85409,RMVar_hsa_circ_225485,RMVar_hsa_circ_225483,RMVar_hsa_circ_343723,RMVar_hsa_circ_355929,RMVar_hsa_circ_51052,RMVar_hsa_circ_99709,RMVar_hsa_circ_351817,RMVar_hsa_circ_225495,RMVar_hsa_circ_5131,RMVar_hsa_circ_726,RMVar_hsa_circ_22253,RMVar_hsa_circ_39688,RMVar_hsa_circ_225502,RMVar_hsa_circ_85345,RMVar_hsa_circ_80805,RMVar_hsa_circ_45042,RMVar_hsa_circ_225503,RMVar_hsa_circ_66244,RMVar_hsa_circ_225507,RMVar_hsa_circ_127738,RMVar_hsa_circ_225505,RMVar_hsa_circ_225504,RMVar_hsa_circ_45539,RMVar_hsa_circ_332594,RMVar_hsa_circ_41370,RMVar_hsa_circ_28222,RMVar_hsa_circ_30234,RMVar_hsa_circ_225510,RMVar_hsa_circ_225511,RMVar_hsa_circ_269628,RMVar_hsa_circ_89608,RMVar_hsa_circ_110839,RMVar_hsa_circ_225513,RMVar_hsa_circ_356874,RMVar_hsa_circ_225512,RMVar_hsa_circ_34344,RMVar_hsa_circ_225515,RMVar_hsa_circ_320638,RMVar_hsa_circ_351336,RMVar_hsa_circ_342706,RMVar_hsa_circ_296369,RMVar_hsa_circ_52835,RMVar_hsa_circ_25099,RMVar_hsa_circ_32771,RMVar_hsa_circ_68087,RMVar_hsa_circ_225516,RMVar_hsa_circ_225517,RMVar_hsa_circ_313124,RMVar_hsa_circ_345031,RMVar_hsa_circ_225523,RMVar_hsa_circ_340629,RMVar_hsa_circ_323243,RMVar_hsa_circ_316763,RMVar_hsa_circ_115099,RMVar_hsa_circ_117011,RMVar_hsa_circ_101014,RMVar_hsa_circ_43045,RMVar_hsa_circ_225526,RMVar_hsa_circ_225530,RMVar_hsa_circ_67338,RMVar_hsa_circ_20180,RMVar_hsa_circ_225528,RMVar_hsa_circ_225529,RMVar_hsa_circ_225527,RMVar_hsa_circ_225524,RMVar_hsa_circ_225525,RMVar_hsa_circ_353523,RMVar_hsa_circ_370364,RMVar_hsa_circ_309019,RMVar_hsa_circ_104888,RMVar_hsa_circ_52264,RMVar_hsa_circ_225535,RMVar_hsa_circ_225537,RMVar_hsa_circ_26094,RMVar_hsa_circ_225536,RMVar_hsa_circ_72227,RMVar_hsa_circ_6863,RMVar_hsa_circ_44268,RMVar_hsa_circ_8174,RMVar_hsa_circ_347851,RMVar_hsa_circ_225538,RMVar_hsa_circ_369150,RMVar_hsa_circ_372517,RMVar_hsa_circ_308361,RMVar_hsa_circ_352955,RMVar_hsa_circ_359849,RMVar_hsa_circ_371148,RMVar_hsa_circ_351920,RMVar_hsa_circ_35262,RMVar_hsa_circ_58738,RMVar_hsa_circ_11264,RMVar_hsa_circ_225541,RMVar_hsa_circ_225543,RMVar_hsa_circ_225544,RMVar_hsa_circ_225542,RMVar_hsa_circ_225540 3080 RMVar_ID_3080 Human_SNP_ID_180892650 A-to-I Human chr4 - 39897522 39897522 39897522 TGGTGGTACATGCCTGTAATCTGAGCTACTCAAGAGGCTGAGACAGGAGAATTGCTTGAACTCGG TGGTGGTACATGCCTGTAATCTGAGCTACTCAGGAGGCTGAGACAGGAGAATTGCTTGAACTCGG T C PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1366280229 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118437,RMVar_hsa_circ_127708,RMVar_hsa_circ_120167,RMVar_hsa_circ_117569,RMVar_hsa_circ_30984,RMVar_hsa_circ_225482,RMVar_hsa_circ_225484,RMVar_hsa_circ_225486,RMVar_hsa_circ_85409,RMVar_hsa_circ_225485,RMVar_hsa_circ_225483,RMVar_hsa_circ_343723,RMVar_hsa_circ_355929,RMVar_hsa_circ_51052,RMVar_hsa_circ_99709,RMVar_hsa_circ_351817,RMVar_hsa_circ_225495,RMVar_hsa_circ_5131,RMVar_hsa_circ_726,RMVar_hsa_circ_22253,RMVar_hsa_circ_39688,RMVar_hsa_circ_225502,RMVar_hsa_circ_85345,RMVar_hsa_circ_80805,RMVar_hsa_circ_45042,RMVar_hsa_circ_225503,RMVar_hsa_circ_66244,RMVar_hsa_circ_225507,RMVar_hsa_circ_127738,RMVar_hsa_circ_225505,RMVar_hsa_circ_225504,RMVar_hsa_circ_45539,RMVar_hsa_circ_332594,RMVar_hsa_circ_41370,RMVar_hsa_circ_28222,RMVar_hsa_circ_30234,RMVar_hsa_circ_225510,RMVar_hsa_circ_225511,RMVar_hsa_circ_269628,RMVar_hsa_circ_89608,RMVar_hsa_circ_110839,RMVar_hsa_circ_225513,RMVar_hsa_circ_356874,RMVar_hsa_circ_225512,RMVar_hsa_circ_34344,RMVar_hsa_circ_225515,RMVar_hsa_circ_320638,RMVar_hsa_circ_351336,RMVar_hsa_circ_342706,RMVar_hsa_circ_296369,RMVar_hsa_circ_52835,RMVar_hsa_circ_25099,RMVar_hsa_circ_32771,RMVar_hsa_circ_68087,RMVar_hsa_circ_225516,RMVar_hsa_circ_225517,RMVar_hsa_circ_313124,RMVar_hsa_circ_345031,RMVar_hsa_circ_225523,RMVar_hsa_circ_340629,RMVar_hsa_circ_323243,RMVar_hsa_circ_316763,RMVar_hsa_circ_115099,RMVar_hsa_circ_117011,RMVar_hsa_circ_101014,RMVar_hsa_circ_43045,RMVar_hsa_circ_225526,RMVar_hsa_circ_225530,RMVar_hsa_circ_67338,RMVar_hsa_circ_20180,RMVar_hsa_circ_225528,RMVar_hsa_circ_225529,RMVar_hsa_circ_225527,RMVar_hsa_circ_225524,RMVar_hsa_circ_225525,RMVar_hsa_circ_353523,RMVar_hsa_circ_370364,RMVar_hsa_circ_309019,RMVar_hsa_circ_104888,RMVar_hsa_circ_52264,RMVar_hsa_circ_225535,RMVar_hsa_circ_225537,RMVar_hsa_circ_26094,RMVar_hsa_circ_225536,RMVar_hsa_circ_72227,RMVar_hsa_circ_6863,RMVar_hsa_circ_44268,RMVar_hsa_circ_8174,RMVar_hsa_circ_347851,RMVar_hsa_circ_225538,RMVar_hsa_circ_369150,RMVar_hsa_circ_372517,RMVar_hsa_circ_308361,RMVar_hsa_circ_352955,RMVar_hsa_circ_359849,RMVar_hsa_circ_371148,RMVar_hsa_circ_351920,RMVar_hsa_circ_35262,RMVar_hsa_circ_58738,RMVar_hsa_circ_11264,RMVar_hsa_circ_225541,RMVar_hsa_circ_225543,RMVar_hsa_circ_225544,RMVar_hsa_circ_225542,RMVar_hsa_circ_225540 3081 RMVar_ID_3081 Human_SNP_ID_180894376 A-to-I Human chr4 - 39904471 39904471 39904471 AATTAGCCGGGCGTGCGGGCGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATGGTG AATTAGCCGGGCGTGCGGGCGCCTGTAGTCCCTGCTACTTGGGAGGCTGAGGCAGGAGAATGGTG T A PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1191466625 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118437,RMVar_hsa_circ_127708,RMVar_hsa_circ_30984,RMVar_hsa_circ_225482,RMVar_hsa_circ_225484,RMVar_hsa_circ_85409,RMVar_hsa_circ_225483,RMVar_hsa_circ_343723,RMVar_hsa_circ_99709,RMVar_hsa_circ_351817,RMVar_hsa_circ_225495,RMVar_hsa_circ_5131,RMVar_hsa_circ_726,RMVar_hsa_circ_225502,RMVar_hsa_circ_85345,RMVar_hsa_circ_80805,RMVar_hsa_circ_225503,RMVar_hsa_circ_225507,RMVar_hsa_circ_127738,RMVar_hsa_circ_225504,RMVar_hsa_circ_45539,RMVar_hsa_circ_332594,RMVar_hsa_circ_41370,RMVar_hsa_circ_28222,RMVar_hsa_circ_30234,RMVar_hsa_circ_225510,RMVar_hsa_circ_225511,RMVar_hsa_circ_110839,RMVar_hsa_circ_225513,RMVar_hsa_circ_356874,RMVar_hsa_circ_34344,RMVar_hsa_circ_225515,RMVar_hsa_circ_351336,RMVar_hsa_circ_342706,RMVar_hsa_circ_52835,RMVar_hsa_circ_25099,RMVar_hsa_circ_68087,RMVar_hsa_circ_225516,RMVar_hsa_circ_323243,RMVar_hsa_circ_316763,RMVar_hsa_circ_115099,RMVar_hsa_circ_117011,RMVar_hsa_circ_101014,RMVar_hsa_circ_43045,RMVar_hsa_circ_225526,RMVar_hsa_circ_67338,RMVar_hsa_circ_20180,RMVar_hsa_circ_225527,RMVar_hsa_circ_225524,RMVar_hsa_circ_225525,RMVar_hsa_circ_104888,RMVar_hsa_circ_52264,RMVar_hsa_circ_225537,RMVar_hsa_circ_26094,RMVar_hsa_circ_6863,RMVar_hsa_circ_44268,RMVar_hsa_circ_70418,RMVar_hsa_circ_74225,RMVar_hsa_circ_276699,RMVar_hsa_circ_8174,RMVar_hsa_circ_225538,RMVar_hsa_circ_369150,RMVar_hsa_circ_372517,RMVar_hsa_circ_359849,RMVar_hsa_circ_35262,RMVar_hsa_circ_58738,RMVar_hsa_circ_11264,RMVar_hsa_circ_341778,RMVar_hsa_circ_225543,RMVar_hsa_circ_225544,RMVar_hsa_circ_368371,RMVar_hsa_circ_367359,RMVar_hsa_circ_345208,RMVar_hsa_circ_307971,RMVar_hsa_circ_314668,RMVar_hsa_circ_307754,RMVar_hsa_circ_62955,RMVar_hsa_circ_225547,RMVar_hsa_circ_225548,RMVar_hsa_circ_225545,RMVar_hsa_circ_225546,RMVar_hsa_circ_88327,RMVar_hsa_circ_2615,RMVar_hsa_circ_106235,RMVar_hsa_circ_225552,RMVar_hsa_circ_36189,RMVar_hsa_circ_68479,RMVar_hsa_circ_374618,RMVar_hsa_circ_375956,RMVar_hsa_circ_74747,RMVar_hsa_circ_96882,RMVar_hsa_circ_71320,RMVar_hsa_circ_348959,RMVar_hsa_circ_225554,RMVar_hsa_circ_225556,RMVar_hsa_circ_225557,RMVar_hsa_circ_225555,RMVar_hsa_circ_359806,RMVar_hsa_circ_282603,RMVar_hsa_circ_337191,RMVar_hsa_circ_276709,RMVar_hsa_circ_225563,RMVar_hsa_circ_293585,RMVar_hsa_circ_225558,RMVar_hsa_circ_225560,RMVar_hsa_circ_225559,RMVar_hsa_circ_315391,RMVar_hsa_circ_316456,RMVar_hsa_circ_360791,RMVar_hsa_circ_313938,RMVar_hsa_circ_73270,RMVar_hsa_circ_286923,RMVar_hsa_circ_225564,RMVar_hsa_circ_225562 3082 RMVar_ID_3082 Human_SNP_ID_180894602 A-to-I Human chr4 - 39905310 39905310 39905310 CAGGTGATCCACCTGCCTCGGCCTCCCAAAGTACTAGGGTTACAGGTGTGAGCCACCATGCCCGC CAGGTGATCCACCTGCCTCGGCCTCCCAAAGTGCTAGGGTTACAGGTGTGAGCCACCATGCCCGC T C PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1465599660 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118437,RMVar_hsa_circ_127708,RMVar_hsa_circ_30984,RMVar_hsa_circ_225482,RMVar_hsa_circ_225484,RMVar_hsa_circ_85409,RMVar_hsa_circ_225483,RMVar_hsa_circ_343723,RMVar_hsa_circ_99709,RMVar_hsa_circ_351817,RMVar_hsa_circ_225495,RMVar_hsa_circ_5131,RMVar_hsa_circ_726,RMVar_hsa_circ_225502,RMVar_hsa_circ_85345,RMVar_hsa_circ_80805,RMVar_hsa_circ_225503,RMVar_hsa_circ_225507,RMVar_hsa_circ_127738,RMVar_hsa_circ_225504,RMVar_hsa_circ_45539,RMVar_hsa_circ_332594,RMVar_hsa_circ_41370,RMVar_hsa_circ_28222,RMVar_hsa_circ_30234,RMVar_hsa_circ_225510,RMVar_hsa_circ_225511,RMVar_hsa_circ_110839,RMVar_hsa_circ_225513,RMVar_hsa_circ_356874,RMVar_hsa_circ_34344,RMVar_hsa_circ_225515,RMVar_hsa_circ_351336,RMVar_hsa_circ_342706,RMVar_hsa_circ_52835,RMVar_hsa_circ_25099,RMVar_hsa_circ_68087,RMVar_hsa_circ_225516,RMVar_hsa_circ_323243,RMVar_hsa_circ_316763,RMVar_hsa_circ_115099,RMVar_hsa_circ_117011,RMVar_hsa_circ_101014,RMVar_hsa_circ_43045,RMVar_hsa_circ_225526,RMVar_hsa_circ_67338,RMVar_hsa_circ_20180,RMVar_hsa_circ_225527,RMVar_hsa_circ_225524,RMVar_hsa_circ_225525,RMVar_hsa_circ_104888,RMVar_hsa_circ_52264,RMVar_hsa_circ_225537,RMVar_hsa_circ_26094,RMVar_hsa_circ_6863,RMVar_hsa_circ_44268,RMVar_hsa_circ_70418,RMVar_hsa_circ_74225,RMVar_hsa_circ_276699,RMVar_hsa_circ_8174,RMVar_hsa_circ_225538,RMVar_hsa_circ_369150,RMVar_hsa_circ_372517,RMVar_hsa_circ_359849,RMVar_hsa_circ_35262,RMVar_hsa_circ_58738,RMVar_hsa_circ_11264,RMVar_hsa_circ_341778,RMVar_hsa_circ_225543,RMVar_hsa_circ_225544,RMVar_hsa_circ_368371,RMVar_hsa_circ_367359,RMVar_hsa_circ_345208,RMVar_hsa_circ_307971,RMVar_hsa_circ_314668,RMVar_hsa_circ_307754,RMVar_hsa_circ_62955,RMVar_hsa_circ_225547,RMVar_hsa_circ_225548,RMVar_hsa_circ_225545,RMVar_hsa_circ_225546,RMVar_hsa_circ_88327,RMVar_hsa_circ_2615,RMVar_hsa_circ_106235,RMVar_hsa_circ_225552,RMVar_hsa_circ_36189,RMVar_hsa_circ_68479,RMVar_hsa_circ_374618,RMVar_hsa_circ_375956,RMVar_hsa_circ_74747,RMVar_hsa_circ_96882,RMVar_hsa_circ_71320,RMVar_hsa_circ_348959,RMVar_hsa_circ_225554,RMVar_hsa_circ_225556,RMVar_hsa_circ_225557,RMVar_hsa_circ_225555,RMVar_hsa_circ_359806,RMVar_hsa_circ_282603,RMVar_hsa_circ_337191,RMVar_hsa_circ_276709,RMVar_hsa_circ_225563,RMVar_hsa_circ_293585,RMVar_hsa_circ_225558,RMVar_hsa_circ_225560,RMVar_hsa_circ_225559,RMVar_hsa_circ_315391,RMVar_hsa_circ_316456,RMVar_hsa_circ_360791,RMVar_hsa_circ_313938,RMVar_hsa_circ_73270,RMVar_hsa_circ_286923,RMVar_hsa_circ_225564,RMVar_hsa_circ_225562 3083 RMVar_ID_3083 Human_SNP_ID_180896171 A-to-I Human chr4 - 39910911 39910911 39910911 CAAGGCTGATCTTGAACTCCTGAGTGCAAGCAATCCACCCACCTCAGCTTCCTGAGTAATAGCTG CAAGGCTGATCTTGAACTCCTGAGTGCAAGCAGTCCACCCACCTCAGCTTCCTGAGTAATAGCTG T C PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs371142452 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118437,RMVar_hsa_circ_127708,RMVar_hsa_circ_30984,RMVar_hsa_circ_225482,RMVar_hsa_circ_225484,RMVar_hsa_circ_85409,RMVar_hsa_circ_225483,RMVar_hsa_circ_343723,RMVar_hsa_circ_99709,RMVar_hsa_circ_351817,RMVar_hsa_circ_225495,RMVar_hsa_circ_5131,RMVar_hsa_circ_225502,RMVar_hsa_circ_85345,RMVar_hsa_circ_80805,RMVar_hsa_circ_225503,RMVar_hsa_circ_225507,RMVar_hsa_circ_127738,RMVar_hsa_circ_225504,RMVar_hsa_circ_45539,RMVar_hsa_circ_332594,RMVar_hsa_circ_28222,RMVar_hsa_circ_225510,RMVar_hsa_circ_225511,RMVar_hsa_circ_110839,RMVar_hsa_circ_225513,RMVar_hsa_circ_356874,RMVar_hsa_circ_225515,RMVar_hsa_circ_351336,RMVar_hsa_circ_342706,RMVar_hsa_circ_52835,RMVar_hsa_circ_25099,RMVar_hsa_circ_68087,RMVar_hsa_circ_225516,RMVar_hsa_circ_316763,RMVar_hsa_circ_115099,RMVar_hsa_circ_117011,RMVar_hsa_circ_101014,RMVar_hsa_circ_225526,RMVar_hsa_circ_67338,RMVar_hsa_circ_225527,RMVar_hsa_circ_225524,RMVar_hsa_circ_225525,RMVar_hsa_circ_104888,RMVar_hsa_circ_52264,RMVar_hsa_circ_225537,RMVar_hsa_circ_26094,RMVar_hsa_circ_6863,RMVar_hsa_circ_44268,RMVar_hsa_circ_70418,RMVar_hsa_circ_74225,RMVar_hsa_circ_8174,RMVar_hsa_circ_225538,RMVar_hsa_circ_369150,RMVar_hsa_circ_372517,RMVar_hsa_circ_359849,RMVar_hsa_circ_35262,RMVar_hsa_circ_58738,RMVar_hsa_circ_11264,RMVar_hsa_circ_341778,RMVar_hsa_circ_225543,RMVar_hsa_circ_225544,RMVar_hsa_circ_368371,RMVar_hsa_circ_367359,RMVar_hsa_circ_345208,RMVar_hsa_circ_314668,RMVar_hsa_circ_307754,RMVar_hsa_circ_62955,RMVar_hsa_circ_225547,RMVar_hsa_circ_225548,RMVar_hsa_circ_225545,RMVar_hsa_circ_225546,RMVar_hsa_circ_88327,RMVar_hsa_circ_106235,RMVar_hsa_circ_225552,RMVar_hsa_circ_36189,RMVar_hsa_circ_68479,RMVar_hsa_circ_374618,RMVar_hsa_circ_74747,RMVar_hsa_circ_96882,RMVar_hsa_circ_71320,RMVar_hsa_circ_225556,RMVar_hsa_circ_225557,RMVar_hsa_circ_225555,RMVar_hsa_circ_359806,RMVar_hsa_circ_282603,RMVar_hsa_circ_276709,RMVar_hsa_circ_22161,RMVar_hsa_circ_225563,RMVar_hsa_circ_293585,RMVar_hsa_circ_225558,RMVar_hsa_circ_315391,RMVar_hsa_circ_316456,RMVar_hsa_circ_73270,RMVar_hsa_circ_286923,RMVar_hsa_circ_225564,RMVar_hsa_circ_10704,RMVar_hsa_circ_318980,RMVar_hsa_circ_337899,RMVar_hsa_circ_295293,RMVar_hsa_circ_225565,RMVar_hsa_circ_225566,RMVar_hsa_circ_333015,RMVar_hsa_circ_378534,RMVar_hsa_circ_36166 3084 RMVar_ID_3084 Human_SNP_ID_180896172 A-to-I Human chr4 - 39910912 39910912 39910912 TCAAGGCTGATCTTGAACTCCTGAGTGCAAGCAATCCACCCACCTCAGCTTCCTGAGTAATAGCT TCAAGGCTGATCTTGAACTCCTGAGTGCAAGCGATCCACCCACCTCAGCTTCCTGAGTAATAGCT T C PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886811978 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15151352 RMVar_hsa_circ_118437,RMVar_hsa_circ_127708,RMVar_hsa_circ_30984,RMVar_hsa_circ_225482,RMVar_hsa_circ_225484,RMVar_hsa_circ_85409,RMVar_hsa_circ_225483,RMVar_hsa_circ_343723,RMVar_hsa_circ_99709,RMVar_hsa_circ_351817,RMVar_hsa_circ_225495,RMVar_hsa_circ_5131,RMVar_hsa_circ_225502,RMVar_hsa_circ_85345,RMVar_hsa_circ_80805,RMVar_hsa_circ_225503,RMVar_hsa_circ_225507,RMVar_hsa_circ_127738,RMVar_hsa_circ_225504,RMVar_hsa_circ_45539,RMVar_hsa_circ_332594,RMVar_hsa_circ_28222,RMVar_hsa_circ_225510,RMVar_hsa_circ_225511,RMVar_hsa_circ_110839,RMVar_hsa_circ_225513,RMVar_hsa_circ_356874,RMVar_hsa_circ_225515,RMVar_hsa_circ_351336,RMVar_hsa_circ_342706,RMVar_hsa_circ_52835,RMVar_hsa_circ_25099,RMVar_hsa_circ_68087,RMVar_hsa_circ_225516,RMVar_hsa_circ_316763,RMVar_hsa_circ_115099,RMVar_hsa_circ_117011,RMVar_hsa_circ_101014,RMVar_hsa_circ_225526,RMVar_hsa_circ_67338,RMVar_hsa_circ_225527,RMVar_hsa_circ_225524,RMVar_hsa_circ_225525,RMVar_hsa_circ_104888,RMVar_hsa_circ_52264,RMVar_hsa_circ_225537,RMVar_hsa_circ_26094,RMVar_hsa_circ_6863,RMVar_hsa_circ_44268,RMVar_hsa_circ_70418,RMVar_hsa_circ_74225,RMVar_hsa_circ_8174,RMVar_hsa_circ_225538,RMVar_hsa_circ_369150,RMVar_hsa_circ_372517,RMVar_hsa_circ_359849,RMVar_hsa_circ_35262,RMVar_hsa_circ_58738,RMVar_hsa_circ_11264,RMVar_hsa_circ_341778,RMVar_hsa_circ_225543,RMVar_hsa_circ_225544,RMVar_hsa_circ_368371,RMVar_hsa_circ_367359,RMVar_hsa_circ_345208,RMVar_hsa_circ_314668,RMVar_hsa_circ_307754,RMVar_hsa_circ_62955,RMVar_hsa_circ_225547,RMVar_hsa_circ_225548,RMVar_hsa_circ_225545,RMVar_hsa_circ_225546,RMVar_hsa_circ_88327,RMVar_hsa_circ_106235,RMVar_hsa_circ_225552,RMVar_hsa_circ_36189,RMVar_hsa_circ_68479,RMVar_hsa_circ_374618,RMVar_hsa_circ_74747,RMVar_hsa_circ_96882,RMVar_hsa_circ_71320,RMVar_hsa_circ_225556,RMVar_hsa_circ_225557,RMVar_hsa_circ_225555,RMVar_hsa_circ_359806,RMVar_hsa_circ_282603,RMVar_hsa_circ_276709,RMVar_hsa_circ_22161,RMVar_hsa_circ_225563,RMVar_hsa_circ_293585,RMVar_hsa_circ_225558,RMVar_hsa_circ_315391,RMVar_hsa_circ_316456,RMVar_hsa_circ_73270,RMVar_hsa_circ_286923,RMVar_hsa_circ_225564,RMVar_hsa_circ_10704,RMVar_hsa_circ_318980,RMVar_hsa_circ_337899,RMVar_hsa_circ_295293,RMVar_hsa_circ_225565,RMVar_hsa_circ_225566,RMVar_hsa_circ_333015,RMVar_hsa_circ_378534,RMVar_hsa_circ_36166 3085 RMVar_ID_3085 Human_SNP_ID_180896813 A-to-I Human chr4 - 39913245 39913244 39913245 TGGTGTCTCTACTAAAAATACAAAAATTAACCAGGGGTGGTGACCGGCACCTGGAACCGCAACTA TGGTGTCTCTACTAAAAATACAAAAATTAACC_GGGGTGGTGACCGGCACCTGGAACCGCAACTA CT C PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1332145447 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_118437,RMVar_hsa_circ_127708,RMVar_hsa_circ_30984,RMVar_hsa_circ_225482,RMVar_hsa_circ_225484,RMVar_hsa_circ_85409,RMVar_hsa_circ_225483,RMVar_hsa_circ_343723,RMVar_hsa_circ_99709,RMVar_hsa_circ_351817,RMVar_hsa_circ_225495,RMVar_hsa_circ_5131,RMVar_hsa_circ_225502,RMVar_hsa_circ_85345,RMVar_hsa_circ_80805,RMVar_hsa_circ_225503,RMVar_hsa_circ_225507,RMVar_hsa_circ_127738,RMVar_hsa_circ_225504,RMVar_hsa_circ_45539,RMVar_hsa_circ_332594,RMVar_hsa_circ_28222,RMVar_hsa_circ_225510,RMVar_hsa_circ_225511,RMVar_hsa_circ_110839,RMVar_hsa_circ_225513,RMVar_hsa_circ_356874,RMVar_hsa_circ_225515,RMVar_hsa_circ_351336,RMVar_hsa_circ_342706,RMVar_hsa_circ_52835,RMVar_hsa_circ_25099,RMVar_hsa_circ_68087,RMVar_hsa_circ_225516,RMVar_hsa_circ_316763,RMVar_hsa_circ_115099,RMVar_hsa_circ_117011,RMVar_hsa_circ_101014,RMVar_hsa_circ_225526,RMVar_hsa_circ_67338,RMVar_hsa_circ_225527,RMVar_hsa_circ_225524,RMVar_hsa_circ_225525,RMVar_hsa_circ_104888,RMVar_hsa_circ_52264,RMVar_hsa_circ_225537,RMVar_hsa_circ_26094,RMVar_hsa_circ_6863,RMVar_hsa_circ_44268,RMVar_hsa_circ_70418,RMVar_hsa_circ_74225,RMVar_hsa_circ_8174,RMVar_hsa_circ_225538,RMVar_hsa_circ_369150,RMVar_hsa_circ_372517,RMVar_hsa_circ_359849,RMVar_hsa_circ_35262,RMVar_hsa_circ_58738,RMVar_hsa_circ_11264,RMVar_hsa_circ_341778,RMVar_hsa_circ_225543,RMVar_hsa_circ_225544,RMVar_hsa_circ_368371,RMVar_hsa_circ_367359,RMVar_hsa_circ_345208,RMVar_hsa_circ_314668,RMVar_hsa_circ_307754,RMVar_hsa_circ_62955,RMVar_hsa_circ_225547,RMVar_hsa_circ_225548,RMVar_hsa_circ_225545,RMVar_hsa_circ_225546,RMVar_hsa_circ_88327,RMVar_hsa_circ_106235,RMVar_hsa_circ_225552,RMVar_hsa_circ_36189,RMVar_hsa_circ_68479,RMVar_hsa_circ_374618,RMVar_hsa_circ_74747,RMVar_hsa_circ_96882,RMVar_hsa_circ_71320,RMVar_hsa_circ_225556,RMVar_hsa_circ_225557,RMVar_hsa_circ_225555,RMVar_hsa_circ_359806,RMVar_hsa_circ_282603,RMVar_hsa_circ_276709,RMVar_hsa_circ_22161,RMVar_hsa_circ_225563,RMVar_hsa_circ_293585,RMVar_hsa_circ_225558,RMVar_hsa_circ_315391,RMVar_hsa_circ_316456,RMVar_hsa_circ_73270,RMVar_hsa_circ_286923,RMVar_hsa_circ_225564,RMVar_hsa_circ_10704,RMVar_hsa_circ_318980,RMVar_hsa_circ_337899,RMVar_hsa_circ_295293,RMVar_hsa_circ_225565,RMVar_hsa_circ_225566,RMVar_hsa_circ_333015,RMVar_hsa_circ_378534,RMVar_hsa_circ_36166 3086 RMVar_ID_3086 Human_SNP_ID_180906542 A-to-I Human chr4 - 39949180 39949180 39949180 CTCCTGCCTCAGCTTCCTGAGTAGCTGGGACTATGGACATGTGCCACCACACCTGGCTATCTTTT CTCCTGCCTCAGCTTCCTGAGTAGCTGGGACTGTGGACATGTGCCACCACACCTGGCTATCTTTT T C PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs903876992 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118437,RMVar_hsa_circ_225482,RMVar_hsa_circ_115099,RMVar_hsa_circ_101014,RMVar_hsa_circ_225524,RMVar_hsa_circ_225525,RMVar_hsa_circ_52264,RMVar_hsa_circ_62955,RMVar_hsa_circ_5363 3087 RMVar_ID_3087 Human_SNP_ID_180907804 A-to-I Human chr4 - 39953548 39953547 39953548 ATTTAAATTTTTAGTAGAGACAAGGTCTCACTATGTTTTCCAGGCTGGTCTTAAACTTTTGGGCT ATTTAAATTTTTAGTAGAGACAAGGTCTCACT_TGTTTTCCAGGCTGGTCTTAAACTTTTGGGCT AT A PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1199730286 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_118437,RMVar_hsa_circ_225482,RMVar_hsa_circ_115099,RMVar_hsa_circ_101014,RMVar_hsa_circ_225524,RMVar_hsa_circ_225525,RMVar_hsa_circ_52264,RMVar_hsa_circ_62955,RMVar_hsa_circ_5363 3088 RMVar_ID_3088 Human_SNP_ID_180907807 A-to-I Human chr4 - 39953558 39953558 39953558 CCCAGCTACAATTTAAATTTTTAGTAGAGACAAGGTCTCACTATGTTTTCCAGGCTGGTCTTAAA CCCAGCTACAATTTAAATTTTTAGTAGAGACAGGGTCTCACTATGTTTTCCAGGCTGGTCTTAAA T C PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1230726558 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118437,RMVar_hsa_circ_225482,RMVar_hsa_circ_115099,RMVar_hsa_circ_101014,RMVar_hsa_circ_225524,RMVar_hsa_circ_225525,RMVar_hsa_circ_52264,RMVar_hsa_circ_62955,RMVar_hsa_circ_5363 3089 RMVar_ID_3089 Human_SNP_ID_180907808 A-to-I Human chr4 - 39953559 39953559 39953559 ACCCAGCTACAATTTAAATTTTTAGTAGAGACAAGGTCTCACTATGTTTTCCAGGCTGGTCTTAA ACCCAGCTACAATTTAAATTTTTAGTAGAGACCAGGTCTCACTATGTTTTCCAGGCTGGTCTTAA T G PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1183861130 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118437,RMVar_hsa_circ_225482,RMVar_hsa_circ_115099,RMVar_hsa_circ_101014,RMVar_hsa_circ_225524,RMVar_hsa_circ_225525,RMVar_hsa_circ_52264,RMVar_hsa_circ_62955,RMVar_hsa_circ_5363 3090 RMVar_ID_3090 Human_SNP_ID_180907809 A-to-I Human chr4 - 39953568 39953568 39953568 TGTCACTACACCCAGCTACAATTTAAATTTTTAGTAGAGACAAGGTCTCACTATGTTTTCCAGGC TGTCACTACACCCAGCTACAATTTAAATTTTTTGTAGAGACAAGGTCTCACTATGTTTTCCAGGC T A PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs984400856 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118437,RMVar_hsa_circ_225482,RMVar_hsa_circ_115099,RMVar_hsa_circ_101014,RMVar_hsa_circ_225524,RMVar_hsa_circ_225525,RMVar_hsa_circ_52264,RMVar_hsa_circ_62955,RMVar_hsa_circ_5363 3091 RMVar_ID_3091 Human_SNP_ID_180907810 A-to-I Human chr4 - 39953568 39953568 39953568 TGTCACTACACCCAGCTACAATTTAAATTTTTAGTAGAGACAAGGTCTCACTATGTTTTCCAGGC TGTCACTACACCCAGCTACAATTTAAATTTTTCGTAGAGACAAGGTCTCACTATGTTTTCCAGGC T G PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs984400856 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118437,RMVar_hsa_circ_225482,RMVar_hsa_circ_115099,RMVar_hsa_circ_101014,RMVar_hsa_circ_225524,RMVar_hsa_circ_225525,RMVar_hsa_circ_52264,RMVar_hsa_circ_62955,RMVar_hsa_circ_5363 3092 RMVar_ID_3092 Human_SNP_ID_180907926 A-to-I Human chr4 - 39954098 39954098 39954098 AGGCTCTAGCAGTCCTCCCACCTCGGCCTCCCAAAGTGCTGAGATTACAGGCGTGGGCCACCATG AGGCTCTAGCAGTCCTCCCACCTCGGCCTCCCGAAGTGCTGAGATTACAGGCGTGGGCCACCATG T C PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1323309677 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118437,RMVar_hsa_circ_225482,RMVar_hsa_circ_115099,RMVar_hsa_circ_101014,RMVar_hsa_circ_225524,RMVar_hsa_circ_225525,RMVar_hsa_circ_52264,RMVar_hsa_circ_62955,RMVar_hsa_circ_5363 3093 RMVar_ID_3093 Human_SNP_ID_180907947 A-to-I Human chr4 - 39954169 39954169 39954169 CTGTTTGTTTGTTTTTTTTTCTCCGTAGAGATAGAGCCTCACTATGTTGTCCAGGATGCTGTCAA CTGTTTGTTTGTTTTTTTTTCTCCGTAGAGATGGAGCCTCACTATGTTGTCCAGGATGCTGTCAA T C PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs921562984 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15151834 RMVar_hsa_circ_118437,RMVar_hsa_circ_225482,RMVar_hsa_circ_115099,RMVar_hsa_circ_101014,RMVar_hsa_circ_225524,RMVar_hsa_circ_225525,RMVar_hsa_circ_52264,RMVar_hsa_circ_62955,RMVar_hsa_circ_5363 3094 RMVar_ID_3094 Human_SNP_ID_180907974 A-to-I Human chr4 - 39954251 39954251 39954251 GGCTCAAGCAATCCTCCCACCTCAGCCTCCTAAGTAACTGGGACTACAGGCACATGCCACCCTGC GGCTCAAGCAATCCTCCCACCTCAGCCTCCTACGTAACTGGGACTACAGGCACATGCCACCCTGC T G PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1005561669 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118437,RMVar_hsa_circ_225482,RMVar_hsa_circ_115099,RMVar_hsa_circ_101014,RMVar_hsa_circ_225524,RMVar_hsa_circ_225525,RMVar_hsa_circ_52264,RMVar_hsa_circ_62955,RMVar_hsa_circ_5363 3095 RMVar_ID_3095 Human_SNP_ID_180907975 A-to-I Human chr4 - 39954252 39954252 39954252 GGGCTCAAGCAATCCTCCCACCTCAGCCTCCTAAGTAACTGGGACTACAGGCACATGCCACCCTG GGGCTCAAGCAATCCTCCCACCTCAGCCTCCTGAGTAACTGGGACTACAGGCACATGCCACCCTG T C PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1246389449 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118437,RMVar_hsa_circ_225482,RMVar_hsa_circ_115099,RMVar_hsa_circ_101014,RMVar_hsa_circ_225524,RMVar_hsa_circ_225525,RMVar_hsa_circ_52264,RMVar_hsa_circ_62955,RMVar_hsa_circ_5363 3096 RMVar_ID_3096 Human_SNP_ID_180908519 A-to-I Human chr4 - 39955952 39955952 39955952 CACCACCATGTCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCGCCATGTTGGCCAGGC CACCACCATGTCTGGCTAATTTTTGTATTTTTGGTAGAGATGGGGTTTCGCCATGTTGGCCAGGC T C PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs931094402 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118437,RMVar_hsa_circ_225482,RMVar_hsa_circ_115099,RMVar_hsa_circ_101014,RMVar_hsa_circ_225524,RMVar_hsa_circ_225525,RMVar_hsa_circ_52264,RMVar_hsa_circ_62955,RMVar_hsa_circ_5363 3097 RMVar_ID_3097 Human_SNP_ID_180908642 A-to-I Human chr4 - 39956381 39956381 39956381 TCAAGCGATCCTCCCACCTCAGCCTCCCAAGTAGCTGGGACTACAGGCATGAGCCACCATACCTG TCAAGCGATCCTCCCACCTCAGCCTCCCAAGTGGCTGGGACTACAGGCATGAGCCACCATACCTG T C PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1356584525 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118437,RMVar_hsa_circ_225482,RMVar_hsa_circ_115099,RMVar_hsa_circ_101014,RMVar_hsa_circ_225524,RMVar_hsa_circ_225525,RMVar_hsa_circ_52264,RMVar_hsa_circ_62955,RMVar_hsa_circ_5363 3098 RMVar_ID_3098 Human_SNP_ID_180908644 A-to-I Human chr4 - 39956398 39956398 39956398 ACTTCTGCCTCCTGGGTTCAAGCGATCCTCCCACCTCAGCCTCCCAAGTAGCTGGGACTACAGGC ACTTCTGCCTCCTGGGTTCAAGCGATCCTCCCTCCTCAGCCTCCCAAGTAGCTGGGACTACAGGC T A PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs571251720 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118437,RMVar_hsa_circ_225482,RMVar_hsa_circ_115099,RMVar_hsa_circ_101014,RMVar_hsa_circ_225524,RMVar_hsa_circ_225525,RMVar_hsa_circ_52264,RMVar_hsa_circ_62955,RMVar_hsa_circ_5363 3099 RMVar_ID_3099 Human_SNP_ID_180909448 A-to-I Human chr4 - 39959375 39959375 39959375 TGTGCTCCAGCCTAGACGACAGTGAGATACCTATCTCCAACAACAACAAAAAAATTTAGATTAAA TGTGCTCCAGCCTAGACGACAGTGAGATACCTGTCTCCAACAACAACAAAAAAATTTAGATTAAA T C PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs887750985 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8591461 RMVar_hsa_circ_118437,RMVar_hsa_circ_225482,RMVar_hsa_circ_115099,RMVar_hsa_circ_101014,RMVar_hsa_circ_225524,RMVar_hsa_circ_225525,RMVar_hsa_circ_52264,RMVar_hsa_circ_62955,RMVar_hsa_circ_5363 3100 RMVar_ID_3100 Human_SNP_ID_180910061 A-to-I Human chr4 - 39961593 39961593 39961593 GCTCTGTAGTTCCAGACCAGCTTGGGCAAAATAGTGAGACCCAGACTCTATTAAAAAGGAAAGAT GCTCTGTAGTTCCAGACCAGCTTGGGCAAAATGGTGAGACCCAGACTCTATTAAAAAGGAAAGAT T C PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs750830963 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118437,RMVar_hsa_circ_225482,RMVar_hsa_circ_115099,RMVar_hsa_circ_101014,RMVar_hsa_circ_225524,RMVar_hsa_circ_225525,RMVar_hsa_circ_52264,RMVar_hsa_circ_62955,RMVar_hsa_circ_5363 3101 RMVar_ID_3101 Human_SNP_ID_180910582 A-to-I Human chr4 - 39963372 39963372 39963372 TTACTGCAACCTCCGCCTTCTAGGTTCAGGCGATTCTCCTGCCTCAGCCCCCTGAGTAGCTGGTA TTACTGCAACCTCCGCCTTCTAGGTTCAGGCGGTTCTCCTGCCTCAGCCCCCTGAGTAGCTGGTA T C PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1433483199 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118437,RMVar_hsa_circ_225482,RMVar_hsa_circ_115099,RMVar_hsa_circ_101014,RMVar_hsa_circ_225524,RMVar_hsa_circ_225525,RMVar_hsa_circ_52264,RMVar_hsa_circ_62955,RMVar_hsa_circ_5363 3102 RMVar_ID_3102 Human_SNP_ID_180913442 A-to-I Human chr4 - 39973818 39973818 39973818 CCCGGTCTTGCAGCACGGTTCTGAGTCTGTGGAATAGCTGCCATGAAGTAACCTGAAGGAGGTGC CCCGGTCTTGCAGCACGGTTCTGAGTCTGTGGGATAGCTGCCATGAAGTAACCTGAAGGAGGTGC T C PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878904637 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15152020 RMVar_hsa_circ_118437,RMVar_hsa_circ_225482,RMVar_hsa_circ_115099,RMVar_hsa_circ_101014,RMVar_hsa_circ_225524,RMVar_hsa_circ_225525,RMVar_hsa_circ_52264,RMVar_hsa_circ_62955,RMVar_hsa_circ_5363 3103 RMVar_ID_3103 Human_SNP_ID_180932808 A-to-I Human chr4 - 40042962 40042962 40042962 CTGGGAGGCAGAGGTTGCAGTGAGCCAAGATCATGCCACTGCTCTCCAGCCTGGGCAACAAGAGC CTGGGAGGCAGAGGTTGCAGTGAGCCAAGATCCTGCCACTGCTCTCCAGCCTGGGCAACAAGAGC T G AC098591.2 Ensembl:ENSG00000205794 Pseudogene exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1046455263 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10161396 3104 RMVar_ID_3104 Human_SNP_ID_180932828 A-to-I Human chr4 - 40043040 40043040 40043040 CAAAACTTAACTGGGCGTGGTGGCAGGCGCCTATAATCCCAGCTACTCAGGAGGCTGAGGCAGGA CAAAACTTAACTGGGCGTGGTGGCAGGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGA T C AC098591.2 Ensembl:ENSG00000205794 Pseudogene exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1294034207 Functional Loss SNV dbSNP153 33..33 33 - - - 3105 RMVar_ID_3105 Human_SNP_ID_180932849 A-to-I Human chr4 - 40043103 40043103 40043103 TTGACGTCAGGAGTTCAAGACCAGCCTAGCCAACATGGCAAAACCCCATCTCTACTAAAAATACA TTGACGTCAGGAGTTCAAGACCAGCCTAGCCAGCATGGCAAAACCCCATCTCTACTAAAAATACA T C AC098591.2 Ensembl:ENSG00000205794 Pseudogene exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs919609714 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10161397 3106 RMVar_ID_3106 Human_SNP_ID_180940982 A-to-I Human chr4 + 40074884 40074884 40074884 CAAAAATTAGTGGGACATGTTGGCATGCACCTATAATCCCAGCTACTTGGGAGGCTGAGACATGA CAAAAATTAGTGGGACATGTTGGCATGCACCTGTAATCCCAGCTACTTGGGAGGCTGAGACATGA A G N4BP2 Ensembl:ENSG00000078177 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1219045956 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2185,RMVar_hsa_circ_334032,RMVar_hsa_circ_367649,RMVar_hsa_circ_269801,RMVar_hsa_circ_314669,RMVar_hsa_circ_51232,RMVar_hsa_circ_225581,RMVar_hsa_circ_225582,RMVar_hsa_circ_225583,RMVar_hsa_circ_225580 3107 RMVar_ID_3107 Human_SNP_ID_180977995 A-to-I Human chr4 + 40229540 40229540 40229540 CCTGTAGTCTGAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCTTGGGGGTGGAGGTT CCTGTAGTCTGAGCTACTCGGGAGGCTGAGGCGGGAGAATCGCTTGAACCTTGGGGGTGGAGGTT A G RHOH Ensembl:ENSG00000168421 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1293437791 Functional Loss SNV dbSNP153 33..33 33 - - - 3108 RMVar_ID_3108 Human_SNP_ID_180977996 A-to-I Human chr4 + 40229540 40229540 40229540 CCTGTAGTCTGAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCTTGGGGGTGGAGGTT CCTGTAGTCTGAGCTACTCGGGAGGCTGAGGCTGGAGAATCGCTTGAACCTTGGGGGTGGAGGTT A T RHOH Ensembl:ENSG00000168421 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1293437791 Functional Loss SNV dbSNP153 33..33 33 - - - 3109 RMVar_ID_3109 Human_SNP_ID_180979400 A-to-I Human chr4 + 40235505 40235505 40235505 CCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCCAGGAGGTGGAGATTGCAGTGAGC CCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCAGGAGGTGGAGATTGCAGTGAGC A G RHOH Ensembl:ENSG00000168421 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1443913321 Functional Loss SNV dbSNP153 33..33 33 - - - 3110 RMVar_ID_3110 Human_SNP_ID_181032627 A-to-I Human chr4 - 40439554 40439554 40439554 CAAATCTTTGAATGCTTCACACCAAGAATTTTACCTGAATGCCACCATCAAAATCAGATTAGCTC CAAATCTTTGAATGCTTCACACCAAGAATTTTGCCTGAATGCCACCATCAAAATCAGATTAGCTC T C RBM47 Ensembl:ENSG00000163694 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10446543 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58228,RMVar_hsa_circ_225606,RMVar_hsa_circ_127719,RMVar_hsa_circ_77299,RMVar_hsa_circ_225608 3111 RMVar_ID_3111 Human_SNP_ID_181037123 A-to-I Human chr4 - 40459895 40459895 40459895 AAAATTAGCTATAGGCATGGTGGCACATGCCTATAATCCCAGCTACCCGGGAGGCTGAGGCAGGA AAAATTAGCTATAGGCATGGTGGCACATGCCTGTAATCCCAGCTACCCGGGAGGCTGAGGCAGGA T C RBM47 Ensembl:ENSG00000163694 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1400563092 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58228,RMVar_hsa_circ_225606,RMVar_hsa_circ_127719,RMVar_hsa_circ_77299,RMVar_hsa_circ_225608 3112 RMVar_ID_3112 Human_SNP_ID_181051075 A-to-I Human chr4 - 40518154 40518153 40518154 AAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAAGAAAAGAAACAATGCTTGTTTTGTGGTGTGAT AAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAA_GAAAAGAAACAATGCTTGTTTTGTGGTGTGAT CT C RBM47 Ensembl:ENSG00000163694 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1396558744 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_225606,RMVar_hsa_circ_127719,RMVar_hsa_circ_77299,RMVar_hsa_circ_329208,RMVar_hsa_circ_225608,RMVar_hsa_circ_340546,RMVar_hsa_circ_225609 3113 RMVar_ID_3113 Human_SNP_ID_181073586 A-to-I Human chr4 - 40604505 40604505 40604505 CTCCCTCCTCAGCCTCCCAAGTAGCTGAGACTACAGGCAGGTACCACCATGCCTGGCTAATTTTT CTCCCTCCTCAGCCTCCCAAGTAGCTGAGACTCCAGGCAGGTACCACCATGCCTGGCTAATTTTT T G RBM47 Ensembl:ENSG00000163694 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1405875605 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_225606,RMVar_hsa_circ_127719,RMVar_hsa_circ_77299,RMVar_hsa_circ_329208,RMVar_hsa_circ_225608,RMVar_hsa_circ_356268,RMVar_hsa_circ_79553,RMVar_hsa_circ_225611 3114 RMVar_ID_3114 Human_SNP_ID_181127246 A-to-I Human chr4 - 40824008 40824008 40824008 TTTAGTAGAGACAGGGTTTCACCGTGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAAATGATC TTTAGTAGAGACAGGGTTTCACCGTGTTGGCCGGGCTGGTCTCGAACTCCTGACCTCAAATGATC T C APBB2 Ensembl:ENSG00000163697 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs955050841 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_225619,RMVar_hsa_circ_308604,RMVar_hsa_circ_225622,RMVar_hsa_circ_75653,RMVar_hsa_circ_92794,RMVar_hsa_circ_27151,RMVar_hsa_circ_225621 3115 RMVar_ID_3115 Human_SNP_ID_181173702 A-to-I Human chr4 - 41004618 41004618 41004618 GTTAGGCAGGATGGTCTCGATCTCCTGACCTCATGATCCACCCGCCTTGCCCAAAGTGCTGGGAT GTTAGGCAGGATGGTCTCGATCTCCTGACCTCGTGATCCACCCGCCTTGCCCAAAGTGCTGGGAT T C APBB2 Ensembl:ENSG00000163697 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs926468558 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_225622,RMVar_hsa_circ_75653,RMVar_hsa_circ_92794,RMVar_hsa_circ_225621,RMVar_hsa_circ_74397,RMVar_hsa_circ_63287,RMVar_hsa_circ_106814,RMVar_hsa_circ_367502,RMVar_hsa_circ_68066,RMVar_hsa_circ_24060,RMVar_hsa_circ_116296,RMVar_hsa_circ_225633,RMVar_hsa_circ_225634,RMVar_hsa_circ_225635 3116 RMVar_ID_3116 Human_SNP_ID_181199019 A-to-I Human chr4 - 41109258 41109258 41109258 GTGATTTTTTTCTTTTTTTAGTGTAGAGAGATAGGGTCTTGCCCTGTCGCCTAGGCTGGAGTGCA GTGATTTTTTTCTTTTTTTAGTGTAGAGAGATGGGGTCTTGCCCTGTCGCCTAGGCTGGAGTGCA T C APBB2 Ensembl:ENSG00000163697 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs530036869 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106814,RMVar_hsa_circ_24060,RMVar_hsa_circ_225633,RMVar_hsa_circ_349374,RMVar_hsa_circ_225643,RMVar_hsa_circ_225642,RMVar_hsa_circ_333959,RMVar_hsa_circ_225640,RMVar_hsa_circ_345081,RMVar_hsa_circ_293141 3117 RMVar_ID_3117 Human_SNP_ID_181234884 A-to-I Human chr4 + 41262275 41262275 41262275 CTTGAGCCCAGGAGTTTGAGACCAGCTTGGCCAACATAGTGAAACCCCGTCCCTACAAAAAATAC CTTGAGCCCAGGAGTTTGAGACCAGCTTGGCCCACATAGTGAAACCCCGTCCCTACAAAAAATAC A C UCHL1 Ensembl:ENSG00000154277 Protein coding intron GSE47997;GSE107867;GSE107867 K562 cells&HepG2 cells;ASD brains,Fragile X samples from NIH NeuroBioBank;ASD brains,frontal_cortex - 23474544,30559470,30559470 RNA-Seq:(High) rs1346061731 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36945,RMVar_hsa_circ_119649,RMVar_hsa_circ_85865,RMVar_hsa_circ_225647,RMVar_hsa_circ_225649,RMVar_hsa_circ_117143,RMVar_hsa_circ_122368,RMVar_hsa_circ_225650,RMVar_hsa_circ_88600,RMVar_hsa_circ_94312,RMVar_hsa_circ_225652,RMVar_hsa_circ_225653,RMVar_hsa_circ_86535,RMVar_hsa_circ_225654,RMVar_hsa_circ_225655 3118 RMVar_ID_3118 Human_SNP_ID_181234886 A-to-I Human chr4 + 41262278 41262278 41262278 GAGCCCAGGAGTTTGAGACCAGCTTGGCCAACATAGTGAAACCCCGTCCCTACAAAAAATACAGA GAGCCCAGGAGTTTGAGACCAGCTTGGCCAACGTAGTGAAACCCCGTCCCTACAAAAAATACAGA A G UCHL1 Ensembl:ENSG00000154277 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1257968950 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36945,RMVar_hsa_circ_119649,RMVar_hsa_circ_85865,RMVar_hsa_circ_225647,RMVar_hsa_circ_225649,RMVar_hsa_circ_117143,RMVar_hsa_circ_122368,RMVar_hsa_circ_225650,RMVar_hsa_circ_88600,RMVar_hsa_circ_94312,RMVar_hsa_circ_225652,RMVar_hsa_circ_225653,RMVar_hsa_circ_86535,RMVar_hsa_circ_225654,RMVar_hsa_circ_225655 3119 RMVar_ID_3119 Human_SNP_ID_181234888 A-to-I Human chr4 + 41262280 41262280 41262280 GCCCAGGAGTTTGAGACCAGCTTGGCCAACATAGTGAAACCCCGTCCCTACAAAAAATACAGAGT GCCCAGGAGTTTGAGACCAGCTTGGCCAACATTGTGAAACCCCGTCCCTACAAAAAATACAGAGT A T UCHL1 Ensembl:ENSG00000154277 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1349913677 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36945,RMVar_hsa_circ_119649,RMVar_hsa_circ_85865,RMVar_hsa_circ_225647,RMVar_hsa_circ_225649,RMVar_hsa_circ_117143,RMVar_hsa_circ_122368,RMVar_hsa_circ_225650,RMVar_hsa_circ_88600,RMVar_hsa_circ_94312,RMVar_hsa_circ_225652,RMVar_hsa_circ_225653,RMVar_hsa_circ_86535,RMVar_hsa_circ_225654,RMVar_hsa_circ_225655 3120 RMVar_ID_3120 Human_SNP_ID_181235678 A-to-I Human chr4 + 41265368 41265368 41265368 GGGAGGCTGACGCGGGAGGATTGCTTGAGCTCAGGAGTTCAAGACCAGCCTGGGCAAAATGGTGA GGGAGGCTGACGCGGGAGGATTGCTTGAGCTCGGGAGTTCAAGACCAGCCTGGGCAAAATGGTGA A G UCHL1 Ensembl:ENSG00000154277 Protein coding intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs774106724 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119649,RMVar_hsa_circ_85865,RMVar_hsa_circ_225647,RMVar_hsa_circ_225649,RMVar_hsa_circ_122368,RMVar_hsa_circ_225650,RMVar_hsa_circ_88600,RMVar_hsa_circ_94312,RMVar_hsa_circ_225653,RMVar_hsa_circ_86535,RMVar_hsa_circ_225654,RMVar_hsa_circ_96952,RMVar_hsa_circ_225655,RMVar_hsa_circ_225657 3121 RMVar_ID_3121 Human_SNP_ID_181260509 A-to-I Human chr4 + 41366887 41366887 41366887 TACTGCCATAAAGATACGACCTGAGACTGGGTAATTTATAAAGAAAGGAGGTTTAACTGACTTAC TACTGCCATAAAGATACGACCTGAGACTGGGTGATTTATAAAGAAAGGAGGTTTAACTGACTTAC A G LIMCH1 Ensembl:ENSG00000064042 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs544468400 Functional Loss SNV dbSNP153 33..33 33 - - - 3122 RMVar_ID_3122 Human_SNP_ID_181270601 A-to-I Human chr4 + 41411869 41411869 41411869 AATCCCAGCTACTCGGGAGGTTGAGGCAGAAGAATTGCTTGAACCCAGGAGGTGGAAGTTGCAGT AATCCCAGCTACTCGGGAGGTTGAGGCAGAAGGATTGCTTGAACCCAGGAGGTGGAAGTTGCAGT A G LIMCH1 Ensembl:ENSG00000064042 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1247208423 Functional Loss SNV dbSNP153 33..33 33 - - - 3123 RMVar_ID_3123 Human_SNP_ID_181277750 A-to-I Human chr4 + 41442255 41442253 41442255 CTGGGAGGTTGAGGCTGCAGTGAGCCATGATTATGTTACTGCCTTCCAGCCTGGGCAACAGAGCC CTGGGAGGTTGAGGCTGCAGTGAGCCATGAT__TGTTACTGCCTTCCAGCCTGGGCAACAGAGCC TTA T LIMCH1 Ensembl:ENSG00000064042 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs796949168 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_25811658 RMVar_hsa_circ_225662 3124 RMVar_ID_3124 Human_SNP_ID_181304009 A-to-I Human chr4 + 41555907 41555907 41555907 GGCACCACAGGCATTTGCTACTGTGTCTGGTTAATTTTTCTTGTACTTTTTGTAGAGACAGGGTT GGCACCACAGGCATTTGCTACTGTGTCTGGTTCATTTTTCTTGTACTTTTTGTAGAGACAGGGTT A C LIMCH1 Ensembl:ENSG00000064042 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs375036708 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15154828 RMVar_hsa_circ_346246,RMVar_hsa_circ_362281,RMVar_hsa_circ_286989,RMVar_hsa_circ_69628 3125 RMVar_ID_3125 Human_SNP_ID_181319306 A-to-I Human chr4 + 41623571 41623571 41623571 CTTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATAGTGAAACCCTGTCTCCACTAAAAGTAC CTTGAGGTCAGGAGTTCAAGACCAGCCTGGCCGACATAGTGAAACCCTGTCTCCACTAAAAGTAC A G LIMCH1 Ensembl:ENSG00000064042 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1166319221 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_362281,RMVar_hsa_circ_69628,RMVar_hsa_circ_64263,RMVar_hsa_circ_225670,RMVar_hsa_circ_47894,RMVar_hsa_circ_26880 3126 RMVar_ID_3126 Human_SNP_ID_181325944 A-to-I Human chr4 + 41650558 41650558 41650558 GGTCTCCACTGGAGCTGAAACAAGACAACGGTAGCATCGAGATCAACATAAAGAAGCCAAACTCT GGTCTCCACTGGAGCTGAAACAAGACAACGGTGGCATCGAGATCAACATAAAGAAGCCAAACTCT A G LIMCH1 Ensembl:ENSG00000064042 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs374137464 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5607427 Human_Splice_Rec_556583,Human_Splice_Rec_556647,Human_Splice_Rec_556697,Human_Splice_Rec_556747,Human_Splice_Rec_556805,Human_Splice_Rec_556857,Human_Splice_Rec_556957,Human_Splice_Rec_557003,Human_Splice_Rec_557041,Human_Splice_Rec_557079,Human_Splice_Rec_557125,Human_Splice_Rec_557163,Human_Splice_Rec_557201 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_38463,RMVar_hsa_circ_225672,RMVar_hsa_circ_225673,RMVar_hsa_circ_225674,RMVar_hsa_circ_55165,RMVar_hsa_circ_301445,RMVar_hsa_circ_225675 3127 RMVar_ID_3127 Human_SNP_ID_181335287 A-to-I Human chr4 + 41692333 41692333 41692333 AGCTTGGAGATGCAGTGAGTGGGACGGATGTTAGGATTCGAAATGGTCTCCTGAACTGTAATGAT AGCTTGGAGATGCAGTGAGTGGGACGGATGTTGGGATTCGAAATGGTCTCCTGAACTGTAATGAT A G LIMCH1 Ensembl:ENSG00000064042 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs766002610 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_72437,Human_RBP_ID_17195671 Human_Splice_Rec_556608,Human_Splice_Rec_556609,Human_Splice_Rec_556670,Human_Splice_Rec_556671,Human_Splice_Rec_556720,Human_Splice_Rec_556721,Human_Splice_Rec_556772,Human_Splice_Rec_556773,Human_Splice_Rec_556822,Human_Splice_Rec_556823,Human_Splice_Rec_556882,Human_Splice_Rec_556883,Human_Splice_Rec_556982,Human_Splice_Rec_556983,Human_Splice_Rec_557026,Human_Splice_Rec_557027,Human_Splice_Rec_557064,Human_Splice_Rec_557065,Human_Splice_Rec_557104,Human_Splice_Rec_557105,Human_Splice_Rec_557148,Human_Splice_Rec_557149,Human_Splice_Rec_557186,Human_Splice_Rec_557187,Human_Splice_Rec_557226,Human_Splice_Rec_557227 RMVar_hsa_circ_4742,RMVar_hsa_circ_69628,RMVar_hsa_circ_225676,RMVar_hsa_circ_55165,RMVar_hsa_circ_338796,RMVar_hsa_circ_293855,RMVar_hsa_circ_52401,RMVar_hsa_circ_31083,RMVar_hsa_circ_225686 3128 RMVar_ID_3128 Human_SNP_ID_181400033 A-to-I Human chr4 + 41958269 41958269 41958269 CTGACCTCGTGATCCCCCCACCTCGGCCTTCCAAAGTGCTGGATTACAGGCGTGAGCCACTGTGC CTGACCTCGTGATCCCCCCACCTCGGCCTTCCTAAGTGCTGGATTACAGGCGTGAGCCACTGTGC A T TMEM33 Ensembl:ENSG00000109133 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs370115166 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8211971,Human_RBP_ID_15156471 3129 RMVar_ID_3129 Human_SNP_ID_181401065 A-to-I Human chr4 + 41962726 41962726 41962726 CTGGACTTTGTGCATGGTGGTTGCACGCCTGTAATCCCAACTACTTGGGAGGCTGAGGTGGGAGA CTGGACTTTGTGCATGGTGGTTGCACGCCTGTCATCCCAACTACTTGGGAGGCTGAGGTGGGAGA A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1051593792 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15156660 3130 RMVar_ID_3130 Human_SNP_ID_181417170 A-to-I Human chr4 + 42029594 42029594 42029594 CCAGAAGGATGACATGATTTTTGAAAATTGTGACAATGTGCCCAGTGAACCCAAAGAACGAGGAG CCAGAAGGATGACATGATTTTTGAAAATTGTGGCAATGTGCCCAGTGAACCCAAAGAACGAGGAG A G ATP1B1P1,SLC30A9 Ensembl:ENSG00000249212,Ensembl:ENSG00000014824 Pseudogene,Protein coding exon,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs878884758 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5102860,Human_RBP_ID_15158007 RMVar_hsa_circ_741,RMVar_hsa_circ_225697,RMVar_hsa_circ_374894,RMVar_hsa_circ_370102,RMVar_hsa_circ_318488,RMVar_hsa_circ_312608,RMVar_hsa_circ_114044,RMVar_hsa_circ_280725,RMVar_hsa_circ_267452,RMVar_hsa_circ_225699,RMVar_hsa_circ_225698,RMVar_hsa_circ_225693,RMVar_hsa_circ_225695,RMVar_hsa_circ_225696,RMVar_hsa_circ_225694,RMVar_hsa_circ_290959,RMVar_hsa_circ_321668,RMVar_hsa_circ_66220,RMVar_hsa_circ_225704,RMVar_hsa_circ_48003,RMVar_hsa_circ_345865,RMVar_hsa_circ_352419,RMVar_hsa_circ_297752,RMVar_hsa_circ_35693,RMVar_hsa_circ_287140,RMVar_hsa_circ_11477,RMVar_hsa_circ_11059,RMVar_hsa_circ_225708,RMVar_hsa_circ_225709,RMVar_hsa_circ_225707,RMVar_hsa_circ_11198,RMVar_hsa_circ_225710 3131 RMVar_ID_3131 Human_SNP_ID_181423118 A-to-I Human chr4 + 42054077 42054077 42054077 TTGTTAACAACCAGAACTGTACATTCTGGGCCAGGTACGGTGGCTCATGCCTGTAATTCCAGCAC TTGTTAACAACCAGAACTGTACATTCTGGGCCCGGTACGGTGGCTCATGCCTGTAATTCCAGCAC A C SLC30A9 Ensembl:ENSG00000014824 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1364392798 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_741,RMVar_hsa_circ_225697,RMVar_hsa_circ_374894,RMVar_hsa_circ_370102,RMVar_hsa_circ_318488,RMVar_hsa_circ_114044,RMVar_hsa_circ_225693,RMVar_hsa_circ_225695,RMVar_hsa_circ_225696,RMVar_hsa_circ_225694,RMVar_hsa_circ_321668,RMVar_hsa_circ_345865,RMVar_hsa_circ_352419,RMVar_hsa_circ_35693,RMVar_hsa_circ_11477,RMVar_hsa_circ_225709,RMVar_hsa_circ_11198,RMVar_hsa_circ_225711,RMVar_hsa_circ_30880,RMVar_hsa_circ_366053 3132 RMVar_ID_3132 Human_SNP_ID_181431297 A-to-I Human chr4 + 42089651 42089651 42089651 GTTGGTCAGGCTGGTCTTGAACTGCCGACCTCAGGTGATCCGCCCTCCTCGGCTTCCCAAAGTGC GTTGGTCAGGCTGGTCTTGAACTGCCGACCTCGGGTGATCCGCCCTCCTCGGCTTCCCAAAGTGC A G SLC30A9 Ensembl:ENSG00000014824 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1394347966 Functional Loss SNV dbSNP153 33..33 33 - - - 3133 RMVar_ID_3133 Human_SNP_ID_181433821 A-to-I Human chr4 - 42099065 42099065 42099065 CAGGAATGAACGCACTCTGATACTCTTGCTAGAATAAGATGGTATTCACCTAATTAGACATAGTT CAGGAATGAACGCACTCTGATACTCTTGCTAGGATAAGATGGTATTCACCTAATTAGACATAGTT T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs565848185 Functional Loss SNV dbSNP153 33..33 33 - - - 3134 RMVar_ID_3134 Human_SNP_ID_181537910 A-to-I Human chr4 - 42508244 42508244 42508244 CCTATAATCCAAGCTACTCTGGAGGCTGAGGCAGGAGAATCACTTGGACCTGGGAGGCGGAGGTT CCTATAATCCAAGCTACTCTGGAGGCTGAGGCGGGAGAATCACTTGGACCTGGGAGGCGGAGGTT T C ATP8A1 Ensembl:ENSG00000124406 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1245501047 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2629,RMVar_hsa_circ_12953,RMVar_hsa_circ_328042,RMVar_hsa_circ_40101,RMVar_hsa_circ_17349,RMVar_hsa_circ_20445,RMVar_hsa_circ_7983,RMVar_hsa_circ_9197,RMVar_hsa_circ_12407,RMVar_hsa_circ_38660,RMVar_hsa_circ_31892,RMVar_hsa_circ_118577,RMVar_hsa_circ_343643,RMVar_hsa_circ_225732,RMVar_hsa_circ_328768,RMVar_hsa_circ_102499,RMVar_hsa_circ_225733,RMVar_hsa_circ_45884,RMVar_hsa_circ_225736,RMVar_hsa_circ_22954,RMVar_hsa_circ_16141,RMVar_hsa_circ_98250,RMVar_hsa_circ_317741,RMVar_hsa_circ_225738,RMVar_hsa_circ_344828,RMVar_hsa_circ_225741,RMVar_hsa_circ_225742,RMVar_hsa_circ_306348,RMVar_hsa_circ_327640,RMVar_hsa_circ_362922,RMVar_hsa_circ_39671,RMVar_hsa_circ_374317,RMVar_hsa_circ_349678,RMVar_hsa_circ_308662,RMVar_hsa_circ_299266,RMVar_hsa_circ_301245,RMVar_hsa_circ_292428,RMVar_hsa_circ_4493,RMVar_hsa_circ_33189,RMVar_hsa_circ_45751,RMVar_hsa_circ_286140,RMVar_hsa_circ_39553,RMVar_hsa_circ_24836,RMVar_hsa_circ_28593,RMVar_hsa_circ_14285,RMVar_hsa_circ_289618,RMVar_hsa_circ_225745,RMVar_hsa_circ_225747,RMVar_hsa_circ_225749,RMVar_hsa_circ_225750,RMVar_hsa_circ_225748,RMVar_hsa_circ_225746,RMVar_hsa_circ_225743,RMVar_hsa_circ_225744,RMVar_hsa_circ_299718,RMVar_hsa_circ_363135,RMVar_hsa_circ_356151,RMVar_hsa_circ_293825,RMVar_hsa_circ_37674,RMVar_hsa_circ_270501,RMVar_hsa_circ_64934,RMVar_hsa_circ_23459,RMVar_hsa_circ_34306,RMVar_hsa_circ_10828,RMVar_hsa_circ_36184,RMVar_hsa_circ_225754,RMVar_hsa_circ_225756,RMVar_hsa_circ_225757,RMVar_hsa_circ_225755,RMVar_hsa_circ_225753,RMVar_hsa_circ_299634,RMVar_hsa_circ_44435,RMVar_hsa_circ_225759,RMVar_hsa_circ_29171 3135 RMVar_ID_3135 Human_SNP_ID_182033941 A-to-I Human chr4 - 44385355 44385355 44385355 TCTAGGCTTTCTATTCTATTTCCTTCGTCTATATGTCTATCTTTATGCCAGTATCACACTGTTTT TCTAGGCTTTCTATTCTATTTCCTTCGTCTATGTGTCTATCTTTATGCCAGTATCACACTGTTTT T C KCTD8 Ensembl:ENSG00000183783 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1328325716 Functional Loss SNV dbSNP153 33..33 33 - - - 3136 RMVar_ID_3136 Human_SNP_ID_218612599 A-to-I Human chr5 - 214786 214786 214786 TGACCTCATGATCTGCCCGCCTCGGCCTCCCAAAGTGCTGGGGTTACAGGTGTGAGCCACCGTGC TGACCTCATGATCTGCCCGCCTCGGCCTCCCATAGTGCTGGGGTTACAGGTGTGAGCCACCGTGC T A CCDC127,AC021087.3 Ensembl:ENSG00000164366,Ensembl:ENSG00000260774 Protein coding,lincRNA intron,exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1029402403 Functional Loss SNV dbSNP153 33..33 33 - - - 3137 RMVar_ID_3137 Human_SNP_ID_218616200 A-to-I Human chr5 + 227080 227080 227080 TCACCCAGGCTGGAGTGCAGTAGCACAATCTCAGCTCACTGCTACTTCCACCTCCTGGATTCAAG TCACCCAGGCTGGAGTGCAGTAGCACAATCTCGGCTCACTGCTACTTCCACCTCCTGGATTCAAG A G SDHA,AC021087.5 Ensembl:ENSG00000073578,Ensembl:ENSG00000286001 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1453327730 Functional Loss SNV dbSNP153 33..33 33 - - - 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 3138 RMVar_ID_3138 Human_SNP_ID_218619692 A-to-I Human chr5 + 238622 238622 238622 GAACTCCTGGCCTCAAGTGTTCCTCCTGTCTCAGCCTCCCGAAGTGGTTACATGCGCCTATACAT GAACTCCTGGCCTCAAGTGTTCCTCCTGTCTCGGCCTCCCGAAGTGGTTACATGCGCCTATACAT A G SDHA,AC021087.5 Ensembl:ENSG00000073578,Ensembl:ENSG00000286001 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1190072742 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_375563,RMVar_hsa_circ_229933,RMVar_hsa_circ_54742,RMVar_hsa_circ_5089,RMVar_hsa_circ_319777,RMVar_hsa_circ_107608,RMVar_hsa_circ_229936,RMVar_hsa_circ_316737,RMVar_hsa_circ_303216,RMVar_hsa_circ_43584,RMVar_hsa_circ_229938,RMVar_hsa_circ_89408,RMVar_hsa_circ_229939,RMVar_hsa_circ_23868,RMVar_hsa_circ_331142 3139 RMVar_ID_3139 Human_SNP_ID_218620089 A-to-I Human chr5 + 239880 239880 239880 CAACCTCCACCTTTAGGGTTCAAGCAGTTCTCATGCCTCAGCCTCCCGAGTAGCTGGGATTATAG CAACCTCCACCTTTAGGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTATAG A C SDHA,AC021087.5 Ensembl:ENSG00000073578,Ensembl:ENSG00000286001 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs768334749 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_375563,RMVar_hsa_circ_229933,RMVar_hsa_circ_54742,RMVar_hsa_circ_5089,RMVar_hsa_circ_319777,RMVar_hsa_circ_107608,RMVar_hsa_circ_229936,RMVar_hsa_circ_316737,RMVar_hsa_circ_303216,RMVar_hsa_circ_43584,RMVar_hsa_circ_229938,RMVar_hsa_circ_89408,RMVar_hsa_circ_229939,RMVar_hsa_circ_23868,RMVar_hsa_circ_331142 3140 RMVar_ID_3140 Human_SNP_ID_218620090 A-to-I Human chr5 + 239880 239880 239880 CAACCTCCACCTTTAGGGTTCAAGCAGTTCTCATGCCTCAGCCTCCCGAGTAGCTGGGATTATAG CAACCTCCACCTTTAGGGTTCAAGCAGTTCTCGTGCCTCAGCCTCCCGAGTAGCTGGGATTATAG A G SDHA,AC021087.5 Ensembl:ENSG00000073578,Ensembl:ENSG00000286001 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs768334749 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_375563,RMVar_hsa_circ_229933,RMVar_hsa_circ_54742,RMVar_hsa_circ_5089,RMVar_hsa_circ_319777,RMVar_hsa_circ_107608,RMVar_hsa_circ_229936,RMVar_hsa_circ_316737,RMVar_hsa_circ_303216,RMVar_hsa_circ_43584,RMVar_hsa_circ_229938,RMVar_hsa_circ_89408,RMVar_hsa_circ_229939,RMVar_hsa_circ_23868,RMVar_hsa_circ_331142 3141 RMVar_ID_3141 Human_SNP_ID_218620091 A-to-I Human chr5 + 239880 239880 239880 CAACCTCCACCTTTAGGGTTCAAGCAGTTCTCATGCCTCAGCCTCCCGAGTAGCTGGGATTATAG CAACCTCCACCTTTAGGGTTCAAGCAGTTCTCTTGCCTCAGCCTCCCGAGTAGCTGGGATTATAG A T SDHA,AC021087.5 Ensembl:ENSG00000073578,Ensembl:ENSG00000286001 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs768334749 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_375563,RMVar_hsa_circ_229933,RMVar_hsa_circ_54742,RMVar_hsa_circ_5089,RMVar_hsa_circ_319777,RMVar_hsa_circ_107608,RMVar_hsa_circ_229936,RMVar_hsa_circ_316737,RMVar_hsa_circ_303216,RMVar_hsa_circ_43584,RMVar_hsa_circ_229938,RMVar_hsa_circ_89408,RMVar_hsa_circ_229939,RMVar_hsa_circ_23868,RMVar_hsa_circ_331142 3142 RMVar_ID_3142 Human_SNP_ID_218629245 A-to-I Human chr5 + 268246 268246 268246 CACTCTGTTGCCCAGGCTGGAGTGCCTGGTGCAATCTCGGCTCACTGCAAGCTCCGCCTCCCGGG CACTCTGTTGCCCAGGCTGGAGTGCCTGGTGCGATCTCGGCTCACTGCAAGCTCCGCCTCCCGGG A G AC021087.5 Ensembl:ENSG00000286001 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1442735152 Functional Loss SNV dbSNP153 33..33 33 - - - 3143 RMVar_ID_3143 Human_SNP_ID_218632156 A-to-I Human chr5 + 277366 277366 277366 CTCTGTCGCCTAGGCTGGAGTGCGGTGGCACTATCTTGGCTCACTGCAAGCTCCGCCTCCTGGGT CTCTGTCGCCTAGGCTGGAGTGCGGTGGCACTGTCTTGGCTCACTGCAAGCTCCGCCTCCTGGGT A G AHRR,AC021087.5,PDCD6 Ensembl:ENSG00000286169,Ensembl:ENSG00000286001,Ensembl:ENSG00000249915 Protein coding,Protein coding,Protein coding intron,intron,intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1484500367 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 3144 RMVar_ID_3144 Human_SNP_ID_218632212 A-to-I Human chr5 + 277562 277562 277562 TGACCTCATGATCCACCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCACGC TGACCTCATGATCCACCCGCCTCAGCCTCCCAGAGTGCTGGGATTACAGGCGTGAGCCACCACGC A G AHRR,AC021087.5,PDCD6 Ensembl:ENSG00000286169,Ensembl:ENSG00000286001,Ensembl:ENSG00000249915 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886491804 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 3145 RMVar_ID_3145 Human_SNP_ID_218632284 A-to-I Human chr5 + 277792 277792 277792 ACAAAATTAGCCGGGAATGGTGGTGCGCGCCTATAATCCCAGCTACTCGGGAGGCTGAGGCGTGA ACAAAATTAGCCGGGAATGGTGGTGCGCGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCGTGA A G AHRR,AC021087.5,PDCD6 Ensembl:ENSG00000286169,Ensembl:ENSG00000286001,Ensembl:ENSG00000249915 Protein coding,Protein coding,Protein coding intron,intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1297733466 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 3146 RMVar_ID_3146 Human_SNP_ID_218642283 A-to-I Human chr5 + 309557 309557 309557 CTGTCCTTCCCCAGCCTTGGCAGGAGACCAGTAATGACCTCTGTCCCCGTGCACCCCAGTGATGG CTGTCCTTCCCCAGCCTTGGCAGGAGACCAGTGATGACCTCTGTCCCCGTGCACCCCAGTGATGG A G AHRR,AC021087.5,PDCD6 Ensembl:ENSG00000286169,Ensembl:ENSG00000286001,Ensembl:ENSG00000249915 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1168304809 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15420117 RMVar_hsa_circ_109933,RMVar_hsa_circ_229944,RMVar_hsa_circ_80928,RMVar_hsa_circ_229943,RMVar_hsa_circ_102611,RMVar_hsa_circ_229945,RMVar_hsa_circ_229946,RMVar_hsa_circ_294234 3147 RMVar_ID_3147 Human_SNP_ID_218643382 A-to-I Human chr5 + 313712 313712 313712 TCTTCTTCTTTCTTGAGACAGACCCTTGCTCCATCACCCAGGCCAGAGTGTGGTGGTGCGAACAC TCTTCTTCTTTCTTGAGACAGACCCTTGCTCCGTCACCCAGGCCAGAGTGTGGTGGTGCGAACAC A G AHRR,AC021087.5,PDCD6 Ensembl:ENSG00000286169,Ensembl:ENSG00000286001,Ensembl:ENSG00000249915 Protein coding,Protein coding,Protein coding intron,3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1478665193 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22612074 Human_Splice_Rec_631004,Human_Splice_Rec_631088 RMVar_hsa_circ_102611,RMVar_hsa_circ_229945,RMVar_hsa_circ_229946 3148 RMVar_ID_3148 Human_SNP_ID_218661809 A-to-I Human chr5 + 383839 383839 383839 TCCCACCCCCGGCCTCCCAAAGTGTTGAGATTACAGGTGTGAGCCACCACACCCAGCCCCCAGCT TCCCACCCCCGGCCTCCCAAAGTGTTGAGATTGCAGGTGTGAGCCACCACACCCAGCCCCCAGCT A G AHRR,AHRR:2 Ensembl:ENSG00000063438,Ensembl:ENSG00000286169 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1197275093 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 3149 RMVar_ID_3149 Human_SNP_ID_218662024 A-to-I Human chr5 + 384891 384891 384891 CTTTAGGCCGGGCGCGGTGGCTCATGCCTGTTATCCCAGCACTTTGGGAGGCTGAGGCAGGCGGA CTTTAGGCCGGGCGCGGTGGCTCATGCCTGTTTTCCCAGCACTTTGGGAGGCTGAGGCAGGCGGA A T AHRR,AHRR:2 Ensembl:ENSG00000063438,Ensembl:ENSG00000286169 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1008476369 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 3150 RMVar_ID_3150 Human_SNP_ID_218669101 A-to-I Human chr5 + 410224 410223 410225 TAACTATTTTATTATTTTATTATTGTAGAGACAGAGTCTCTGTCACCCAGGCTGAAGTGCAGTGG TAACTATTTTATTATTTTATTATTGTAGAGAC__AGTCTCTGTCACCCAGGCTGAAGTGCAGTGG CAG C AHRR,AHRR:2 Ensembl:ENSG00000063438,Ensembl:ENSG00000286169 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1461187711 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_22301044 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 3151 RMVar_ID_3151 Human_SNP_ID_218685453 A-to-I Human chr5 + 461631 461631 461631 CAAGACTCTATCTCAAAAAAAAAAAAAGAGACAAGGTCTGATTAGGTTACCCCGACGGGTAGCTC CAAGACTCTATCTCAAAAAAAAAAAAAGAGACGAGGTCTGATTAGGTTACCCCGACGGGTAGCTC A G EXOC3 Ensembl:ENSG00000180104 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1024683714 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8616844,Human_RBP_ID_15456378 RMVar_hsa_circ_2325,RMVar_hsa_circ_118392,RMVar_hsa_circ_111883,RMVar_hsa_circ_127694,RMVar_hsa_circ_229953,RMVar_hsa_circ_229954,RMVar_hsa_circ_368081,RMVar_hsa_circ_229955,RMVar_hsa_circ_229958,RMVar_hsa_circ_93932,RMVar_hsa_circ_328081,RMVar_hsa_circ_16684,RMVar_hsa_circ_27968 3152 RMVar_ID_3152 Human_SNP_ID_218731732 A-to-I Human chr5 + 613445 613445 613445 CAGGTTGGAGTGCAGTGGCACAATCTCAGCTCACTGCAACCTCCACCTCCCAGGTTCAAGTGATT CAGGTTGGAGTGCAGTGGCACAATCTCAGCTCGCTGCAACCTCCACCTCCCAGGTTCAAGTGATT A G CEP72 Ensembl:ENSG00000112877 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs986560119 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_229961,RMVar_hsa_circ_91841,RMVar_hsa_circ_107458,RMVar_hsa_circ_114656,RMVar_hsa_circ_229962,RMVar_hsa_circ_229963 3153 RMVar_ID_3153 Human_SNP_ID_218731746 A-to-I Human chr5 + 613507 613507 613507 ATTCACTCAGCCTCCTGAGTAGCTGGGATTACAAGCACGCGCCACCATGCCCGGCTAATTTTTTA ATTCACTCAGCCTCCTGAGTAGCTGGGATTACGAGCACGCGCCACCATGCCCGGCTAATTTTTTA A G CEP72 Ensembl:ENSG00000112877 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202489379 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_229961,RMVar_hsa_circ_91841,RMVar_hsa_circ_107458,RMVar_hsa_circ_114656,RMVar_hsa_circ_229962,RMVar_hsa_circ_229963 3154 RMVar_ID_3154 Human_SNP_ID_218731783 A-to-I Human chr5 + 613641 613641 613641 CACCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCTACACCCAGCCTGAGCT CACCTGCCTTGGCCTCCCAAAGTGCTGGGATTGCAGGCATGAGCCACCTACACCCAGCCTGAGCT A G CEP72 Ensembl:ENSG00000112877 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1327880277 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24110988 RMVar_hsa_circ_229961,RMVar_hsa_circ_91841,RMVar_hsa_circ_107458,RMVar_hsa_circ_114656,RMVar_hsa_circ_229962,RMVar_hsa_circ_229963 3155 RMVar_ID_3155 Human_SNP_ID_218731996 A-to-I Human chr5 + 614578 614578 614578 TCATGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGAACTCCTGACCTCATGATCCGCCCACC TCATGCCATTCTCCTGCCTCAGCCTCCCGAGTGGCTGGAACTCCTGACCTCATGATCCGCCCACC A G CEP72 Ensembl:ENSG00000112877 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202418744 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2941510,Human_RBP_ID_7454323,Human_RBP_ID_15479442 RMVar_hsa_circ_229961,RMVar_hsa_circ_91841,RMVar_hsa_circ_107458,RMVar_hsa_circ_114656,RMVar_hsa_circ_229962,RMVar_hsa_circ_229963 3156 RMVar_ID_3156 Human_SNP_ID_218747717 A-to-I Human chr5 - 662915 662915 662915 CGGACTCACCCGATCACAGACGAGCGGTCACCAGAATCGCCCGATCACAGACGAGCAGTCATCGG CGGACTCACCCGATCACAGACGAGCGGTCACCGGAATCGCCCGATCACAGACGAGCAGTCATCGG T C TPPP Ensembl:ENSG00000171368 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs878950282 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78820,RMVar_hsa_circ_229975 3157 RMVar_ID_3157 Human_SNP_ID_218818038 A-to-I Human chr5 - 872930 872930 872930 TAACTCCTGACCTCAAATGATGCATCCATCTCAGCCTCCCAGAGTGGTAGGATGTTGTCTTTTCT TAACTCCTGACCTCAAATGATGCATCCATCTCGGCCTCCCAGAGTGGTAGGATGTTGTCTTTTCT T C BRD9 Ensembl:ENSG00000028310 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1435242861 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80144,RMVar_hsa_circ_229988 3158 RMVar_ID_3158 Human_SNP_ID_218818053 A-to-I Human chr5 - 872982 872982 872982 TTTTGTATTTTTAGTAGAGGCGGAGTTTCGCCATGTTGGCCAGGCTGGTCTTTAACTCCTGACCT TTTTGTATTTTTAGTAGAGGCGGAGTTTCGCCGTGTTGGCCAGGCTGGTCTTTAACTCCTGACCT T C BRD9 Ensembl:ENSG00000028310 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs548980245 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80144,RMVar_hsa_circ_229988 3159 RMVar_ID_3159 Human_SNP_ID_218850134 A-to-I Human chr5 - 991250 991250 991250 CCCTGTCTCTACTAAAAAATACAAAAAAAATTAGTTGGATGTGGTGGCGGGCACCTGTAGTCCCA CCCTGTCTCTACTAAAAAATACAAAAAAAATTTGTTGGATGTGGTGGCGGGCACCTGTAGTCCCA T A AC116351.1 Ensembl:ENSG00000215246 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1422819784 Functional Loss SNV dbSNP153 33..33 33 - - - 3160 RMVar_ID_3160 Human_SNP_ID_218964404 A-to-I Human chr5 - 1324688 1324688 1324688 CCAACACCCTCAAAGACGGGTCTTTTACTGTCATTGCTCAGTGCGGAAGTCTCCTTGGAGTACGG CCAACACCCTCAAAGACGGGTCTTTTACTGTCGTTGCTCAGTGCGGAAGTCTCCTTGGAGTACGG T C CLPTM1L Ensembl:ENSG00000049656 Protein coding intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1490760297 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1644366,Human_RBP_ID_15297552,Human_RBP_ID_27734326 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 3161 RMVar_ID_3161 Human_SNP_ID_218965283 A-to-I Human chr5 + 1326842 1326842 1326842 CCTACAGGGACATTTCATCCAGCTCCTCCTCGACAGACACATTTCATCCAGCTCCTCCTCGACAG CCTACAGGGACATTTCATCCAGCTCCTCCTCGGCAGACACATTTCATCCAGCTCCTCCTCGACAG A G lnc-SLC6A18-1 RNACentral:URS00008B9CC1 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs562359238 Functional Loss SNV dbSNP153 33..33 33 - - - 3162 RMVar_ID_3162 Human_SNP_ID_218965284 A-to-I Human chr5 + 1326844 1326844 1326844 TACAGGGACATTTCATCCAGCTCCTCCTCGACAGACACATTTCATCCAGCTCCTCCTCGACAGAC TACAGGGACATTTCATCCAGCTCCTCCTCGACGGACACATTTCATCCAGCTCCTCCTCGACAGAC A G lnc-SLC6A18-1 RNACentral:URS00008B9CC1 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs201348077 Functional Loss SNV dbSNP153 33..33 33 - - - 3163 RMVar_ID_3163 Human_SNP_ID_218965289 A-to-I Human chr5 + 1326848 1326848 1326848 GGGACATTTCATCCAGCTCCTCCTCGACAGACACATTTCATCCAGCTCCTCCTCGACAGACACAT GGGACATTTCATCCAGCTCCTCCTCGACAGACGCATTTCATCCAGCTCCTCCTCGACAGACACAT A G lnc-SLC6A18-1 RNACentral:URS00008B9CC1 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1431443791 Functional Loss SNV dbSNP153 33..33 33 - - - 3164 RMVar_ID_3164 Human_SNP_ID_218965309 A-to-I Human chr5 - 1326880 1326880 1326880 GAAATGTGTCCGTAGAGGAGGAGCTGGATGAAATGTGTCTGTCGAGGAGGAGCTGGATGAAATGT GAAATGTGTCCGTAGAGGAGGAGCTGGATGAAGTGTGTCTGTCGAGGAGGAGCTGGATGAAATGT T C CLPTM1L Ensembl:ENSG00000049656 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1214204950 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24082781 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 3165 RMVar_ID_3165 Human_SNP_ID_218971773 A-to-I Human chr5 - 1342725 1342725 1342725 AGTTAGCCAGGCATGGTGGCACGCCCACCTGTAGTCCCAGCTACTCGGGAGACTGAGGCGGGAGG AGTTAGCCAGGCATGGTGGCACGCCCACCTGTTGTCCCAGCTACTCGGGAGACTGAGGCGGGAGG T A CLPTM1L Ensembl:ENSG00000049656 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1012137563 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71711,RMVar_hsa_circ_25216 3166 RMVar_ID_3166 Human_SNP_ID_218971785 A-to-I Human chr5 - 1342777 1342777 1342777 CAAGACCAGCCTAGGCAATGTGACAAAACCCCATCTCTACAACAGTTTTCAAAGTTAGCCAGGCA CAAGACCAGCCTAGGCAATGTGACAAAACCCCGTCTCTACAACAGTTTTCAAAGTTAGCCAGGCA T C CLPTM1L Ensembl:ENSG00000049656 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs967761961 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71711,RMVar_hsa_circ_25216 3167 RMVar_ID_3167 Human_SNP_ID_218971809 A-to-I Human chr5 - 1342864 1342864 1342864 TAAGGAGAGGCCGGGCACAGTGACTCATGCCTATAATCCCAGCAGTTTGGGAGGCCAAGGCGGGA TAAGGAGAGGCCGGGCACAGTGACTCATGCCTGTAATCCCAGCAGTTTGGGAGGCCAAGGCGGGA T C CLPTM1L Ensembl:ENSG00000049656 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs757610297 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71711,RMVar_hsa_circ_25216 3168 RMVar_ID_3168 Human_SNP_ID_218971892 A-to-I Human chr5 - 1343083 1343083 1343083 GGGTTCAAGGGATTCTCCTGCCTTAGCCTCCAAAGTAGCTGAGACTACAGGCACCCGCCACCACG GGGTTCAAGGGATTCTCCTGCCTTAGCCTCCAGAGTAGCTGAGACTACAGGCACCCGCCACCACG T C CLPTM1L Ensembl:ENSG00000049656 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1193300451 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71711,RMVar_hsa_circ_25216 3169 RMVar_ID_3169 Human_SNP_ID_218974420 A-to-I Human chr5 + 1351499 1351498 1351500 AAGCACTAGAGTAGAAATTTTTTTTTAGAGACAGGGTCTCGCACCGTCATCCAGGCTGGAGGGCA AAGCACTAGAGTAGAAATTTTTTTTTAGAGAC__GGTCTCGCACCGTCATCCAGGCTGGAGGGCA CAG C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1415354200 Functional Loss DEL dbSNP153 33..34 33 - - - 3170 RMVar_ID_3170 Human_SNP_ID_219108516 A-to-I Human chr5 + 1812906 1812906 1812906 GAAACCCTGTCTCTACTAAAAATACAAAAATTAGTCGGACGTGGTGGCGGGTGCCTGTAATCCCA GAAACCCTGTCTCTACTAAAAATACAAAAATTGGTCGGACGTGGTGGCGGGTGCCTGTAATCCCA A G NDUFS6 Ensembl:ENSG00000145494 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs767308501 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81273,RMVar_hsa_circ_100999,RMVar_hsa_circ_230062,RMVar_hsa_circ_230063 3171 RMVar_ID_3171 Human_SNP_ID_220092380 A-to-I Human chr5 - 5419794 5419794 5419794 AACATATACTTCCACTGAAATGGCTAATAGATATGGTCTAGAAACCAAGGAGAACTCAAAATGGA AACATATACTTCCACTGAAATGGCTAATAGATGTGGTCTAGAAACCAAGGAGAACTCAAAATGGA T C AC091978.1 Ensembl:ENSG00000286753 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1159718007 Functional Loss SNV dbSNP153 33..33 33 - - - 3172 RMVar_ID_3172 Human_SNP_ID_220092382 A-to-I Human chr5 - 5419801 5419801 5419801 GTTTATTAACATATACTTCCACTGAAATGGCTAATAGATATGGTCTAGAAACCAAGGAGAACTCA GTTTATTAACATATACTTCCACTGAAATGGCTGATAGATATGGTCTAGAAACCAAGGAGAACTCA T C AC091978.1 Ensembl:ENSG00000286753 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs911927099 Functional Loss SNV dbSNP153 33..33 33 - - - 3173 RMVar_ID_3173 Human_SNP_ID_220092386 A-to-I Human chr5 - 5419825 5419825 5419825 CATTGAGAGGTAACTGTTGATTTAGTTTATTAACATATACTTCCACTGAAATGGCTAATAGATAT CATTGAGAGGTAACTGTTGATTTAGTTTATTACCATATACTTCCACTGAAATGGCTAATAGATAT T G AC091978.1 Ensembl:ENSG00000286753 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1324360587 Functional Loss SNV dbSNP153 33..33 33 - - - 3174 RMVar_ID_3174 Human_SNP_ID_220410148 A-to-I Human chr5 - 6610124 6610124 6610124 AGGAGGCGGAGGCTACAGTGGGTTGAGATCACACCACTGCACTCCAGCCTAGGCAACAGATCCAG AGGAGGCGGAGGCTACAGTGGGTTGAGATCACGCCACTGCACTCCAGCCTAGGCAACAGATCCAG T C NSUN2 Ensembl:ENSG00000037474 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1560148 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17575361 RMVar_hsa_circ_31359,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_281127,RMVar_hsa_circ_66959,RMVar_hsa_circ_83064,RMVar_hsa_circ_230095,RMVar_hsa_circ_230096,RMVar_hsa_circ_73188,RMVar_hsa_circ_230097 3175 RMVar_ID_3175 Human_SNP_ID_220410149 A-to-I Human chr5 - 6610124 6610124 6610124 AGGAGGCGGAGGCTACAGTGGGTTGAGATCACACCACTGCACTCCAGCCTAGGCAACAGATCCAG AGGAGGCGGAGGCTACAGTGGGTTGAGATCACCCCACTGCACTCCAGCCTAGGCAACAGATCCAG T G NSUN2 Ensembl:ENSG00000037474 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1560148 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17575361 RMVar_hsa_circ_31359,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_281127,RMVar_hsa_circ_66959,RMVar_hsa_circ_83064,RMVar_hsa_circ_230095,RMVar_hsa_circ_230096,RMVar_hsa_circ_73188,RMVar_hsa_circ_230097 3176 RMVar_ID_3176 Human_SNP_ID_220410169 A-to-I Human chr5 - 6610202 6610202 6610202 AAAACTGGCCAGGCAGTGTGTTGCATGCCTGTAGTCCCAGCTCCTTGGGAGGCTGAGGCAGGAGG AAAACTGGCCAGGCAGTGTGTTGCATGCCTGTGGTCCCAGCTCCTTGGGAGGCTGAGGCAGGAGG T C NSUN2 Ensembl:ENSG00000037474 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs904969688 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17575361 RMVar_hsa_circ_31359,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_281127,RMVar_hsa_circ_66959,RMVar_hsa_circ_83064,RMVar_hsa_circ_230095,RMVar_hsa_circ_230096,RMVar_hsa_circ_73188,RMVar_hsa_circ_230097 3177 RMVar_ID_3177 Human_SNP_ID_220410202 A-to-I Human chr5 - 6610278 6610278 6610278 GAGCTCAAAAGTTTGAGACCAGCCTGGACGACATGGCAAGACCCCATCTCTACAGAAAAAAAAAA GAGCTCAAAAGTTTGAGACCAGCCTGGACGACTTGGCAAGACCCCATCTCTACAGAAAAAAAAAA T A NSUN2 Ensembl:ENSG00000037474 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7717596 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_28 GWAS_ID_45,GWAS_ID_46,GWAS_ID_47,GWAS_ID_48,GWAS_ID_49,GWAS_ID_50,GWAS_ID_51,GWAS_ID_52,GWAS_ID_53,GWAS_ID_54,GWAS_ID_55,GWAS_ID_56,GWAS_ID_57,GWAS_ID_58,GWAS_ID_59,GWAS_ID_60,GWAS_ID_61,GWAS_ID_62,GWAS_ID_63,GWAS_ID_64,GWAS_ID_65,GWAS_ID_66,GWAS_ID_67,GWAS_ID_68,GWAS_ID_69,GWAS_ID_70,GWAS_ID_71,GWAS_ID_72,GWAS_ID_73,GWAS_ID_74,GWAS_ID_75,GWAS_ID_76,GWAS_ID_77,GWAS_ID_78,GWAS_ID_79,GWAS_ID_80,GWAS_ID_81,GWAS_ID_82,GWAS_ID_83,GWAS_ID_84,GWAS_ID_85,GWAS_ID_86,GWAS_ID_87,GWAS_ID_88,GWAS_ID_89,GWAS_ID_90,GWAS_ID_91 RMVar_hsa_circ_31359,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_281127,RMVar_hsa_circ_66959,RMVar_hsa_circ_83064,RMVar_hsa_circ_230095,RMVar_hsa_circ_230096,RMVar_hsa_circ_73188,RMVar_hsa_circ_230097 3178 RMVar_ID_3178 Human_SNP_ID_220410203 A-to-I Human chr5 - 6610278 6610278 6610278 GAGCTCAAAAGTTTGAGACCAGCCTGGACGACATGGCAAGACCCCATCTCTACAGAAAAAAAAAA GAGCTCAAAAGTTTGAGACCAGCCTGGACGACGTGGCAAGACCCCATCTCTACAGAAAAAAAAAA T C NSUN2 Ensembl:ENSG00000037474 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7717596 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_28 GWAS_ID_45,GWAS_ID_46,GWAS_ID_47,GWAS_ID_48,GWAS_ID_49,GWAS_ID_50,GWAS_ID_51,GWAS_ID_52,GWAS_ID_53,GWAS_ID_54,GWAS_ID_55,GWAS_ID_56,GWAS_ID_57,GWAS_ID_58,GWAS_ID_59,GWAS_ID_60,GWAS_ID_61,GWAS_ID_62,GWAS_ID_63,GWAS_ID_64,GWAS_ID_65,GWAS_ID_66,GWAS_ID_67,GWAS_ID_68,GWAS_ID_69,GWAS_ID_70,GWAS_ID_71,GWAS_ID_72,GWAS_ID_73,GWAS_ID_74,GWAS_ID_75,GWAS_ID_76,GWAS_ID_77,GWAS_ID_78,GWAS_ID_79,GWAS_ID_80,GWAS_ID_81,GWAS_ID_82,GWAS_ID_83,GWAS_ID_84,GWAS_ID_85,GWAS_ID_86,GWAS_ID_87,GWAS_ID_88,GWAS_ID_89,GWAS_ID_90,GWAS_ID_91 RMVar_hsa_circ_31359,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_281127,RMVar_hsa_circ_66959,RMVar_hsa_circ_83064,RMVar_hsa_circ_230095,RMVar_hsa_circ_230096,RMVar_hsa_circ_73188,RMVar_hsa_circ_230097 3179 RMVar_ID_3179 Human_SNP_ID_220410261 A-to-I Human chr5 - 6610517 6610517 6610517 TGGCTAATTTTTGTATTTTTATTAGTAGAGACAGGGTTTCACCACGTTGGCCAGGCTGGTGTTGA TGGCTAATTTTTGTATTTTTATTAGTAGAGACCGGGTTTCACCACGTTGGCCAGGCTGGTGTTGA T G NSUN2 Ensembl:ENSG00000037474 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1039607205 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_31359,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_281127,RMVar_hsa_circ_66959,RMVar_hsa_circ_83064,RMVar_hsa_circ_230095,RMVar_hsa_circ_230096,RMVar_hsa_circ_73188,RMVar_hsa_circ_230097 3180 RMVar_ID_3180 Human_SNP_ID_220410283 A-to-I Human chr5 - 6610621 6610621 6610621 GGAGTGTAGTAGCTCGATCTCGGCTCACTGCAACCTCTGCCTCCTGGGTTCAAGCAATTCTCGTG GGAGTGTAGTAGCTCGATCTCGGCTCACTGCAGCCTCTGCCTCCTGGGTTCAAGCAATTCTCGTG T C NSUN2 Ensembl:ENSG00000037474 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs959971049 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_31359,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_281127,RMVar_hsa_circ_66959,RMVar_hsa_circ_83064,RMVar_hsa_circ_230095,RMVar_hsa_circ_230096,RMVar_hsa_circ_73188,RMVar_hsa_circ_230097 3181 RMVar_ID_3181 Human_SNP_ID_220424941 A-to-I Human chr5 + 6664578 6664578 6664578 AGGCATGCACCACCAGGCCTGGCTAATTTTTTATATTTTTTGTAGAGTTGTGGTCTCACTATATT AGGCATGCACCACCAGGCCTGGCTAATTTTTTGTATTTTTTGTAGAGTTGTGGTCTCACTATATT A G SRD5A1 Ensembl:ENSG00000145545 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1160357369 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2943797,Human_RBP_ID_15498027,Human_RBP_ID_18845845 RMVar_hsa_circ_230117,RMVar_hsa_circ_230116,RMVar_hsa_circ_90771 3182 RMVar_ID_3182 Human_SNP_ID_220424956 A-to-I Human chr5 + 6664674 6664674 6664674 GTAATCCTCACACCTCAGCCTCCTGAAGTGCTAGGATTCGAGGCGTGAGCCAACGTGGCTGGCCT GTAATCCTCACACCTCAGCCTCCTGAAGTGCTGGGATTCGAGGCGTGAGCCAACGTGGCTGGCCT A G SRD5A1 Ensembl:ENSG00000145545 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005620424 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_230117,RMVar_hsa_circ_230116,RMVar_hsa_circ_90771 3183 RMVar_ID_3183 Human_SNP_ID_220448744 A-to-I Human chr5 + 6756781 6756779 6756781 TTAGCAATATTGACTGTAAACCCACATTAAGGAAACCACTACGGGTCTGGCAGTGCGTGTCCCGT TTAGCAATATTGACTGTAAACCCACATTAAG__AACCACTACGGGTCTGGCAGTGCGTGTCCCGT GGA G TENT4A Ensembl:ENSG00000112941 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1416202311 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_311653,Human_RBP_ID_1657058,Human_RBP_ID_1998511,Human_RBP_ID_15499900,Human_RBP_ID_17530882,Human_RBP_ID_27742944 Human_miRNA_ID_1934333,Human_miRNA_ID_2057427,Human_miRNA_ID_3126377,Human_miRNA_ID_3126530 RMVar_hsa_circ_84254,RMVar_hsa_circ_230123 3184 RMVar_ID_3184 Human_SNP_ID_220708138 A-to-I Human chr5 + 7800505 7800504 7800505 CCAACATGGTGAAACCCTGTCTCTACTAAAATAAAAAAAATTAGCTGGGCATGGTGGTGCACACC CCAACATGGTGAAACCCTGTCTCTACTAAAAT_AAAAAAATTAGCTGGGCATGGTGGTGCACACC TA T ADCY2 Ensembl:ENSG00000078295 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs988447255 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_102794,RMVar_hsa_circ_101285,RMVar_hsa_circ_230126,RMVar_hsa_circ_230127,RMVar_hsa_circ_7061,RMVar_hsa_circ_103710,RMVar_hsa_circ_230147,RMVar_hsa_circ_266397,RMVar_hsa_circ_265018,RMVar_hsa_circ_230150,RMVar_hsa_circ_230149,RMVar_hsa_circ_50426,RMVar_hsa_circ_313873,RMVar_hsa_circ_230151,RMVar_hsa_circ_325758,RMVar_hsa_circ_288019 3185 RMVar_ID_3185 Human_SNP_ID_220708140 A-to-I Human chr5 + 7800505 7800505 7800505 CCAACATGGTGAAACCCTGTCTCTACTAAAATAAAAAAAATTAGCTGGGCATGGTGGTGCACACC CCAACATGGTGAAACCCTGTCTCTACTAAAATGAAAAAAATTAGCTGGGCATGGTGGTGCACACC A G ADCY2 Ensembl:ENSG00000078295 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1262477829 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102794,RMVar_hsa_circ_101285,RMVar_hsa_circ_230126,RMVar_hsa_circ_230127,RMVar_hsa_circ_7061,RMVar_hsa_circ_103710,RMVar_hsa_circ_230147,RMVar_hsa_circ_266397,RMVar_hsa_circ_265018,RMVar_hsa_circ_230150,RMVar_hsa_circ_230149,RMVar_hsa_circ_50426,RMVar_hsa_circ_313873,RMVar_hsa_circ_230151,RMVar_hsa_circ_325758,RMVar_hsa_circ_288019 3186 RMVar_ID_3186 Human_SNP_ID_220708141 A-to-I Human chr5 + 7800510 7800510 7800510 ATGGTGAAACCCTGTCTCTACTAAAATAAAAAAAATTAGCTGGGCATGGTGGTGCACACCTGTAA ATGGTGAAACCCTGTCTCTACTAAAATAAAAATAATTAGCTGGGCATGGTGGTGCACACCTGTAA A T ADCY2 Ensembl:ENSG00000078295 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs912861199 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102794,RMVar_hsa_circ_101285,RMVar_hsa_circ_230126,RMVar_hsa_circ_230127,RMVar_hsa_circ_7061,RMVar_hsa_circ_103710,RMVar_hsa_circ_230147,RMVar_hsa_circ_266397,RMVar_hsa_circ_265018,RMVar_hsa_circ_230150,RMVar_hsa_circ_230149,RMVar_hsa_circ_50426,RMVar_hsa_circ_313873,RMVar_hsa_circ_230151,RMVar_hsa_circ_325758,RMVar_hsa_circ_288019 3187 RMVar_ID_3187 Human_SNP_ID_220714783 A-to-I Human chr5 - 7827636 7827636 7827636 TCTCAATATTGGCTTCTGGAGAGCTCTTTCTGAAACAACTGTGTCAAAAGGGAGAATGGATGGAA TCTCAATATTGGCTTCTGGAGAGCTCTTTCTGCAACAACTGTGTCAAAAGGGAGAATGGATGGAA T G - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs534707508 Functional Loss SNV dbSNP153 33..33 33 - - - 3188 RMVar_ID_3188 Human_SNP_ID_221309876 A-to-I Human chr5 - 10207336 10207336 10207336 GGAGTGCAATGGCGGGATCTTGGCTCACCGCAACCTCTGCCTCCTGGGTTCACGCGATTCTCCTG GGAGTGCAATGGCGGGATCTTGGCTCACCGCAGCCTCTGCCTCCTGGGTTCACGCGATTCTCCTG T C lnc-FAM173B-6 RNACentral:URS00008B378A lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1482618608 Functional Loss SNV dbSNP153 33..33 33 - - - 3189 RMVar_ID_3189 Human_SNP_ID_221310909 A-to-I Human chr5 - 10211736 10211736 10211736 AGCATAGGGGAAACTGCCTCCATGATCCAATTACCTCCGCCTGGTCCCACCTTTGACATGTGGGG AGCATAGGGGAAACTGCCTCCATGATCCAATTTCCTCCGCCTGGTCCCACCTTTGACATGTGGGG T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1174637994 Functional Loss SNV dbSNP153 33..33 33 - - - 3190 RMVar_ID_3190 Human_SNP_ID_221310918 A-to-I Human chr5 - 10211773 10211773 10211773 ATCAGATCTCGTGAGACTCACTCATGATCACAAGAACAGCATAGGGGAAACTGCCTCCATGATCC ATCAGATCTCGTGAGACTCACTCATGATCACAGGAACAGCATAGGGGAAACTGCCTCCATGATCC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973417647 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15248111 3191 RMVar_ID_3191 Human_SNP_ID_221313812 A-to-I Human chr5 - 10223635 10223635 10223635 ATTGTGAGGCTTCCCCAGCCATGTGGAACTGTAAGTCCAGTTAAACCCCTTTATTTTGTAAATTG ATTGTGAGGCTTCCCCAGCCATGTGGAACTGTCAGTCCAGTTAAACCCCTTTATTTTGTAAATTG T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs780478977 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82391,RMVar_hsa_circ_102886,RMVar_hsa_circ_230199,RMVar_hsa_circ_230200,RMVar_hsa_circ_230201 3192 RMVar_ID_3192 Human_SNP_ID_221315144 A-to-I Human chr5 - 10228896 10228896 10228896 GCCAGCTGCAGTGGCTCACGCCTGTAGTCCCAACACTTTGAGAGGCTGAGGTGGGCAGATGGCTT GCCAGCTGCAGTGGCTCACGCCTGTAGTCCCAGCACTTTGAGAGGCTGAGGTGGGCAGATGGCTT T C ATPSCKMT Ensembl:ENSG00000150756 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs919697472 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128006,RMVar_hsa_circ_230199,RMVar_hsa_circ_230203 3193 RMVar_ID_3193 Human_SNP_ID_221329103 A-to-I Human chr5 - 10279627 10279627 10279627 TCTGAGGAGGAGAATCACTTGAACCTGGAGGCAGAGGTTGCAGTGAGTCGAGGTTGCGCTACTGC TCTGAGGAGGAGAATCACTTGAACCTGGAGGCGGAGGTTGCAGTGAGTCGAGGTTGCGCTACTGC T C CMBL Ensembl:ENSG00000164237 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs538531291 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_627573,Human_RBP_ID_8213389,Human_RBP_ID_26529038 RMVar_hsa_circ_103527,RMVar_hsa_circ_230213 3194 RMVar_ID_3194 Human_SNP_ID_221350882 A-to-I Human chr5 + 10359628 10359628 10359628 AATATATTTATTGAAGAAAGAAATCCGCGTATAAGTGGACCCATGTAGTTCAAACTGTGATGTTC AATATATTTATTGAAGAAAGAAATCCGCGTATGAGTGGACCCATGTAGTTCAAACTGTGATGTTC A G MARCHF6 Ensembl:ENSG00000145495 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1413352234 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7356724 RMVar_hsa_circ_230214,RMVar_hsa_circ_86906,RMVar_hsa_circ_116223,RMVar_hsa_circ_230215,RMVar_hsa_circ_230216 3195 RMVar_ID_3195 Human_SNP_ID_221353128 A-to-I Human chr5 + 10368375 10368375 10368375 CACTTCTTGGCCAGGCACATTGGCTCACACCTATAATACTGGCAGTTTGGGAGGCCAACACCAGA CACTTCTTGGCCAGGCACATTGGCTCACACCTGTAATACTGGCAGTTTGGGAGGCCAACACCAGA A G MARCHF6 Ensembl:ENSG00000145495 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs964502433 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17575611 RMVar_hsa_circ_230214,RMVar_hsa_circ_86906,RMVar_hsa_circ_116223,RMVar_hsa_circ_230215,RMVar_hsa_circ_230216 3196 RMVar_ID_3196 Human_SNP_ID_221353129 A-to-I Human chr5 + 10368377 10368377 10368377 CTTCTTGGCCAGGCACATTGGCTCACACCTATAATACTGGCAGTTTGGGAGGCCAACACCAGAGG CTTCTTGGCCAGGCACATTGGCTCACACCTATGATACTGGCAGTTTGGGAGGCCAACACCAGAGG A G MARCHF6 Ensembl:ENSG00000145495 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1273009953 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17575611 RMVar_hsa_circ_230214,RMVar_hsa_circ_86906,RMVar_hsa_circ_116223,RMVar_hsa_circ_230215,RMVar_hsa_circ_230216 3197 RMVar_ID_3197 Human_SNP_ID_221353144 A-to-I Human chr5 + 10368423 10368423 10368423 GGGAGGCCAACACCAGAGGATTGCTTGAGCCCAGGAGTTTGAGACCAGACTGGGCAACGTGGTGA GGGAGGCCAACACCAGAGGATTGCTTGAGCCCGGGAGTTTGAGACCAGACTGGGCAACGTGGTGA A G MARCHF6 Ensembl:ENSG00000145495 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1356363603 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15252991 RMVar_hsa_circ_230214,RMVar_hsa_circ_86906,RMVar_hsa_circ_116223,RMVar_hsa_circ_230215,RMVar_hsa_circ_230216 3198 RMVar_ID_3198 Human_SNP_ID_221353145 A-to-I Human chr5 + 10368423 10368423 10368423 GGGAGGCCAACACCAGAGGATTGCTTGAGCCCAGGAGTTTGAGACCAGACTGGGCAACGTGGTGA GGGAGGCCAACACCAGAGGATTGCTTGAGCCCTGGAGTTTGAGACCAGACTGGGCAACGTGGTGA A T MARCHF6 Ensembl:ENSG00000145495 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1356363603 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15252991 RMVar_hsa_circ_230214,RMVar_hsa_circ_86906,RMVar_hsa_circ_116223,RMVar_hsa_circ_230215,RMVar_hsa_circ_230216 3199 RMVar_ID_3199 Human_SNP_ID_221356439 A-to-I Human chr5 + 10380676 10380676 10380676 GGCCAGGTGCTGTGGCTCACCCCTGTAATTCCAGCACTTTGAAAGGCTGAGGCAGGCGGACCACC GGCCAGGTGCTGTGGCTCACCCCTGTAATTCCTGCACTTTGAAAGGCTGAGGCAGGCGGACCACC A T MARCHF6 Ensembl:ENSG00000145495 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1561112055 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15253393,Human_RBP_ID_17158878 RMVar_hsa_circ_35462,RMVar_hsa_circ_230214,RMVar_hsa_circ_86906,RMVar_hsa_circ_116223,RMVar_hsa_circ_230215,RMVar_hsa_circ_286757,RMVar_hsa_circ_317192,RMVar_hsa_circ_342281,RMVar_hsa_circ_230216,RMVar_hsa_circ_370049,RMVar_hsa_circ_337058,RMVar_hsa_circ_52343,RMVar_hsa_circ_64370,RMVar_hsa_circ_47282,RMVar_hsa_circ_122295,RMVar_hsa_circ_230218,RMVar_hsa_circ_230220,RMVar_hsa_circ_29769,RMVar_hsa_circ_230221,RMVar_hsa_circ_230219,RMVar_hsa_circ_230222 3200 RMVar_ID_3200 Human_SNP_ID_221359687 A-to-I Human chr5 + 10393205 10393205 10393205 CTCCCACCTCAGCTCCCCAAGTAGCTGGGACCACAGATGTGTGCCATCATGCCCAGCTAATTTAG CTCCCACCTCAGCTCCCCAAGTAGCTGGGACCCCAGATGTGTGCCATCATGCCCAGCTAATTTAG A C MARCHF6 Ensembl:ENSG00000145495 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1380411233 Functional Loss SNV dbSNP153 33..33 33 - - - 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_230221,RMVar_hsa_circ_230219,RMVar_hsa_circ_326284,RMVar_hsa_circ_378915,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_361119,RMVar_hsa_circ_354683,RMVar_hsa_circ_267605,RMVar_hsa_circ_267438,RMVar_hsa_circ_34647,RMVar_hsa_circ_73185,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 3201 RMVar_ID_3201 Human_SNP_ID_221405566 A-to-I Human chr5 + 10568718 10568718 10568718 CACCACGCCCGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCATCATGATGGCCAGGCTGG CACCACGCCCGGCTAATTTTTGTATTTTTAGTGGAGACAGGGTTTCATCATGATGGCCAGGCTGG A G ANKRD33B Ensembl:ENSG00000164236 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1056903210 Functional Loss SNV dbSNP153 33..33 33 - - - 3202 RMVar_ID_3202 Human_SNP_ID_221439647 A-to-I Human chr5 - 10694895 10694882 10694896 GAAGCACAAAGCTATGGATTCTGAGCAGAGTCAAAACAAGAGTTTTGGAATTTGCTTCTAGGCTG GAAGCACAAAGCTATGGATTCTGAGCAGAGT______________TGGAATTTGCTTCTAGGCTG AAAACTCTTGTTTTG A DAP Ensembl:ENSG00000112977 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459925629 Functional Loss DEL dbSNP153 32..45 33 - - - RMVar_hsa_circ_107577,RMVar_hsa_circ_230272 3203 RMVar_ID_3203 Human_SNP_ID_221451239 A-to-I Human chr5 - 10741237 10741237 10741237 GCAGTCCTCCCACCTCTGCCTCGCAAGTAGCTAGGACTAGAGGTGTACACCACCACGCTCAGCAA GCAGTCCTCCCACCTCTGCCTCGCAAGTAGCTGGGACTAGAGGTGTACACCACCACGCTCAGCAA T C DAP Ensembl:ENSG00000112977 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1456924864 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107577,RMVar_hsa_circ_230272 3204 RMVar_ID_3204 Human_SNP_ID_221454888 A-to-I Human chr5 - 10755982 10755982 10755982 CACCACAACCAGCTAATTTGTGTATTTTGTGTAGACACAAGGTTTTACTATGTTGTCCAGTCAGG CACCACAACCAGCTAATTTGTGTATTTTGTGTGGACACAAGGTTTTACTATGTTGTCCAGTCAGG T C DAP Ensembl:ENSG00000112977 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs571550404 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92360,RMVar_hsa_circ_107577,RMVar_hsa_circ_230272,RMVar_hsa_circ_230273 3205 RMVar_ID_3205 Human_SNP_ID_221455969 A-to-I Human chr5 - 10759840 10759840 10759840 CGAGGCAGGAGAATGGCTTGAACCCGGGAGGCAGAAGTTGTAGTGAGCCAAGATTGAGCCAAAGC CGAGGCAGGAGAATGGCTTGAACCCGGGAGGCGGAAGTTGTAGTGAGCCAAGATTGAGCCAAAGC T C DAP Ensembl:ENSG00000112977 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1009203879 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92360,RMVar_hsa_circ_107577,RMVar_hsa_circ_230272,RMVar_hsa_circ_230273 3206 RMVar_ID_3206 Human_SNP_ID_221455992 A-to-I Human chr5 - 10759911 10759911 10759911 ATCTCTACTAAAAGTAGAAAAATTAGCTGGGCATGGTGGCGGGCGCCTGTAATCCCAGCTATTCA ATCTCTACTAAAAGTAGAAAAATTAGCTGGGCCTGGTGGCGGGCGCCTGTAATCCCAGCTATTCA T G DAP Ensembl:ENSG00000112977 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs893231040 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92360,RMVar_hsa_circ_107577,RMVar_hsa_circ_230272,RMVar_hsa_circ_230273 3207 RMVar_ID_3207 Human_SNP_ID_221455995 A-to-I Human chr5 - 10759928 10759926 10759929 TAACATGGTGAAACCCCATCTCTACTAAAAGTAGAAAAATTAGCTGGGCATGGTGGCGGGCGCCT TAACATGGTGAAACCCCATCTCTACTAAAAG___AAAAATTAGCTGGGCATGGTGGCGGGCGCCT TCTA T DAP Ensembl:ENSG00000112977 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1028339326 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_92360,RMVar_hsa_circ_107577,RMVar_hsa_circ_230272,RMVar_hsa_circ_230273 3208 RMVar_ID_3208 Human_SNP_ID_221455996 A-to-I Human chr5 - 10759928 10759928 10759928 TAACATGGTGAAACCCCATCTCTACTAAAAGTAGAAAAATTAGCTGGGCATGGTGGCGGGCGCCT TAACATGGTGAAACCCCATCTCTACTAAAAGTGGAAAAATTAGCTGGGCATGGTGGCGGGCGCCT T C DAP Ensembl:ENSG00000112977 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs769553782 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92360,RMVar_hsa_circ_107577,RMVar_hsa_circ_230272,RMVar_hsa_circ_230273 3209 RMVar_ID_3209 Human_SNP_ID_221548007 A-to-I Human chr5 - 11140058 11140058 11140058 AGATGGAATTAAGGTTGCTAACACCTGACCTTAAAATAGGGCGATTATGCTGGATTATTTGCGTG AGATGGAATTAAGGTTGCTAACACCTGACCTTTAAATAGGGCGATTATGCTGGATTATTTGCGTG T A CTNND2 Ensembl:ENSG00000169862 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs985423597 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_632,RMVar_hsa_circ_12164,RMVar_hsa_circ_355063,RMVar_hsa_circ_53089,RMVar_hsa_circ_45828,RMVar_hsa_circ_230280,RMVar_hsa_circ_230281,RMVar_hsa_circ_32604,RMVar_hsa_circ_44282 3210 RMVar_ID_3210 Human_SNP_ID_221708845 A-to-I Human chr5 - 11783589 11783589 11783589 TTGGCAGCTCTTCCCATTTACTACCTGCAGTTATGTCATCTGCTCTATACCTAAAAACCATTATG TTGGCAGCTCTTCCCATTTACTACCTGCAGTTTTGTCATCTGCTCTATACCTAAAAACCATTATG T A CTNND2 Ensembl:ENSG00000169862 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs560506702 Functional Loss SNV dbSNP153 33..33 33 - - - 3211 RMVar_ID_3211 Human_SNP_ID_221708846 A-to-I Human chr5 - 11783589 11783589 11783589 TTGGCAGCTCTTCCCATTTACTACCTGCAGTTATGTCATCTGCTCTATACCTAAAAACCATTATG TTGGCAGCTCTTCCCATTTACTACCTGCAGTTGTGTCATCTGCTCTATACCTAAAAACCATTATG T C CTNND2 Ensembl:ENSG00000169862 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs560506702 Functional Loss SNV dbSNP153 33..33 33 - - - 3212 RMVar_ID_3212 Human_SNP_ID_221718979 A-to-I Human chr5 - 11818474 11818474 11818474 GTTTCAGCTACTTGGGAGGCTGAGGCAGGAGAATTGCTTGAACCCAAGAGGCAGAGGTTGCAGTG GTTTCAGCTACTTGGGAGGCTGAGGCAGGAGAGTTGCTTGAACCCAAGAGGCAGAGGTTGCAGTG T C CTNND2 Ensembl:ENSG00000169862 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1178154592 Functional Loss SNV dbSNP153 33..33 33 - - - 3213 RMVar_ID_3213 Human_SNP_ID_221718999 A-to-I Human chr5 - 11818541 11818541 11818541 CAACATGGTGAAACTGCGTCTCTACTAAGTATACATAAATTAGCTGGGCATGGTGGTGGCAGCTG CAACATGGTGAAACTGCGTCTCTACTAAGTATGCATAAATTAGCTGGGCATGGTGGTGGCAGCTG T C CTNND2 Ensembl:ENSG00000169862 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs915243041 Functional Loss SNV dbSNP153 33..33 33 - - - 3214 RMVar_ID_3214 Human_SNP_ID_221719159 A-to-I Human chr5 - 11819216 11819216 11819216 TTGGCCAGGCTGGTCTCAAACTCCTGACTTCCAGTGATCCGCCGGCCTCAGCCTCCCAAAGTGCT TTGGCCAGGCTGGTCTCAAACTCCTGACTTCCGGTGATCCGCCGGCCTCAGCCTCCCAAAGTGCT T C CTNND2 Ensembl:ENSG00000169862 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1045610727 Functional Loss SNV dbSNP153 33..33 33 - - - 3215 RMVar_ID_3215 Human_SNP_ID_221719162 A-to-I Human chr5 - 11819229 11819228 11819230 GGGTTTCACCACGTTGGCCAGGCTGGTCTCAAACTCCTGACTTCCAGTGATCCGCCGGCCTCAGC GGGTTTCACCACGTTGGCCAGGCTGGTCTCA__CTCCTGACTTCCAGTGATCCGCCGGCCTCAGC GTT G CTNND2 Ensembl:ENSG00000169862 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1436385200 Functional Loss DEL dbSNP153 32..33 33 - - - 3216 RMVar_ID_3216 Human_SNP_ID_221719162 A-to-I Human chr5 - 11819230 11819228 11819230 AGGGTTTCACCACGTTGGCCAGGCTGGTCTCAAACTCCTGACTTCCAGTGATCCGCCGGCCTCAG AGGGTTTCACCACGTTGGCCAGGCTGGTCTCA__CTCCTGACTTCCAGTGATCCGCCGGCCTCAG GTT G CTNND2 Ensembl:ENSG00000169862 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1436385200 Functional Loss DEL dbSNP153 33..34 33 - - - 3217 RMVar_ID_3217 Human_SNP_ID_221719170 A-to-I Human chr5 - 11819262 11819260 11819262 TCCTGGCTAAGTTTTGTATTTTTAGTAGAAACAGGGTTTCACCACGTTGGCCAGGCTGGTCTCAA TCCTGGCTAAGTTTTGTATTTTTAGTAGAAAC__GGTTTCACCACGTTGGCCAGGCTGGTCTCAA CCT C CTNND2 Ensembl:ENSG00000169862 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1449265130 Functional Loss DEL dbSNP153 33..34 33 - - - 3218 RMVar_ID_3218 Human_SNP_ID_221719172 A-to-I Human chr5 - 11819268 11819268 11819268 CACCACTCCTGGCTAAGTTTTGTATTTTTAGTAGAAACAGGGTTTCACCACGTTGGCCAGGCTGG CACCACTCCTGGCTAAGTTTTGTATTTTTAGTGGAAACAGGGTTTCACCACGTTGGCCAGGCTGG T C CTNND2 Ensembl:ENSG00000169862 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs942913367 Functional Loss SNV dbSNP153 33..33 33 - - - 3219 RMVar_ID_3219 Human_SNP_ID_222323738 A-to-I Human chr5 + 14157613 14157612 14157614 CTGTCTCTCTCTTTCTCTCTTTCTTTCGAGACAGGGTCTTGTTCTTGCCCAGGCTGGAGTGCAGT CTGTCTCTCTCTTTCTCTCTTTCTTTCGAGAC__GGTCTTGTTCTTGCCCAGGCTGGAGTGCAGT CAG C TRIO Ensembl:ENSG00000038382 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs565512430 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_18955873,Human_RBP_ID_21130604 RMVar_hsa_circ_77339,RMVar_hsa_circ_94247,RMVar_hsa_circ_93187,RMVar_hsa_circ_230320,RMVar_hsa_circ_230321,RMVar_hsa_circ_230319 3220 RMVar_ID_3220 Human_SNP_ID_222324829 A-to-I Human chr5 + 14161775 14161775 14161775 TTGAGACAGCGTCTCACCCTGTCACCCAGGCTAGAGTTCAGTGGTGTGATTATGGCTTACTGCAG TTGAGACAGCGTCTCACCCTGTCACCCAGGCTGGAGTTCAGTGGTGTGATTATGGCTTACTGCAG A G TRIO Ensembl:ENSG00000038382 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs577347414 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77339,RMVar_hsa_circ_94247,RMVar_hsa_circ_93187,RMVar_hsa_circ_230320,RMVar_hsa_circ_230321,RMVar_hsa_circ_230319 3221 RMVar_ID_3221 Human_SNP_ID_222328578 A-to-I Human chr5 + 14176566 14176566 14176566 GCCTCGATTTTCTGGGCTCAGGCAGTCCTCCTACCTCAGCCTCCCGAGTACCTGGGATTGCAGCC GCCTCGATTTTCTGGGCTCAGGCAGTCCTCCTGCCTCAGCCTCCCGAGTACCTGGGATTGCAGCC A G TRIO Ensembl:ENSG00000038382 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1038150949 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17575366 RMVar_hsa_circ_77339,RMVar_hsa_circ_94247,RMVar_hsa_circ_93187,RMVar_hsa_circ_230320,RMVar_hsa_circ_230321,RMVar_hsa_circ_230319 3222 RMVar_ID_3222 Human_SNP_ID_222329326 A-to-I Human chr5 + 14179515 14179515 14179515 TTAGGGTCTCACTCTGTTGCCCAATTTGGAGCAGTGGCACAATCACGGCTCACTGCAGCCTTGAG TTAGGGTCTCACTCTGTTGCCCAATTTGGAGCGGTGGCACAATCACGGCTCACTGCAGCCTTGAG A G TRIO Ensembl:ENSG00000038382 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1274335830 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77339,RMVar_hsa_circ_94247,RMVar_hsa_circ_93187,RMVar_hsa_circ_230320,RMVar_hsa_circ_230321,RMVar_hsa_circ_230319 3223 RMVar_ID_3223 Human_SNP_ID_222329419 A-to-I Human chr5 + 14179836 14179836 14179836 TTAACTGTCTGGGCATGGTGGCTCAGGTGTGTAATCCCGGCACTCTGGGAGGCTGAGGTGGGTGG TTAACTGTCTGGGCATGGTGGCTCAGGTGTGTTATCCCGGCACTCTGGGAGGCTGAGGTGGGTGG A T TRIO Ensembl:ENSG00000038382 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs901816315 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17575367 RMVar_hsa_circ_77339,RMVar_hsa_circ_94247,RMVar_hsa_circ_93187,RMVar_hsa_circ_230320,RMVar_hsa_circ_230321,RMVar_hsa_circ_230319 3224 RMVar_ID_3224 Human_SNP_ID_222343287 A-to-I Human chr5 + 14233290 14233290 14233290 ATCACTTGAGCCCAGGAGTTCGAGACCAGCCTAGGCAACATGGCGAGACCTCGTCTCTTAAAAAA ATCACTTGAGCCCAGGAGTTCGAGACCAGCCTGGGCAACATGGCGAGACCTCGTCTCTTAAAAAA A G TRIO Ensembl:ENSG00000038382 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1007976040 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77339,RMVar_hsa_circ_94247,RMVar_hsa_circ_93187,RMVar_hsa_circ_107815,RMVar_hsa_circ_230320,RMVar_hsa_circ_230321,RMVar_hsa_circ_230319,RMVar_hsa_circ_230322 3225 RMVar_ID_3225 Human_SNP_ID_222343288 A-to-I Human chr5 + 14233290 14233290 14233290 ATCACTTGAGCCCAGGAGTTCGAGACCAGCCTAGGCAACATGGCGAGACCTCGTCTCTTAAAAAA ATCACTTGAGCCCAGGAGTTCGAGACCAGCCTTGGCAACATGGCGAGACCTCGTCTCTTAAAAAA A T TRIO Ensembl:ENSG00000038382 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1007976040 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77339,RMVar_hsa_circ_94247,RMVar_hsa_circ_93187,RMVar_hsa_circ_107815,RMVar_hsa_circ_230320,RMVar_hsa_circ_230321,RMVar_hsa_circ_230319,RMVar_hsa_circ_230322 3226 RMVar_ID_3226 Human_SNP_ID_222343476 A-to-I Human chr5 + 14233890 14233890 14233890 AGAGCTCACTGCAGACTTGAAATCCTGGGTTCAAGTGATTCTTTCACCTCAGCCTCCTGAGTAGC AGAGCTCACTGCAGACTTGAAATCCTGGGTTCGAGTGATTCTTTCACCTCAGCCTCCTGAGTAGC A G TRIO Ensembl:ENSG00000038382 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1394289503 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77339,RMVar_hsa_circ_94247,RMVar_hsa_circ_93187,RMVar_hsa_circ_107815,RMVar_hsa_circ_230320,RMVar_hsa_circ_230321,RMVar_hsa_circ_230319,RMVar_hsa_circ_230322 3227 RMVar_ID_3227 Human_SNP_ID_222343484 A-to-I Human chr5 + 14233908 14233907 14233909 GAAATCCTGGGTTCAAGTGATTCTTTCACCTCAGCCTCCTGAGTAGCTGGGATTGCAGGTGCATA GAAATCCTGGGTTCAAGTGATTCTTTCACCTC__CCTCCTGAGTAGCTGGGATTGCAGGTGCATA CAG C TRIO Ensembl:ENSG00000038382 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1385248266 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_77339,RMVar_hsa_circ_94247,RMVar_hsa_circ_93187,RMVar_hsa_circ_107815,RMVar_hsa_circ_230320,RMVar_hsa_circ_230321,RMVar_hsa_circ_230319,RMVar_hsa_circ_230322 3228 RMVar_ID_3228 Human_SNP_ID_222343485 A-to-I Human chr5 + 14233908 14233908 14233908 GAAATCCTGGGTTCAAGTGATTCTTTCACCTCAGCCTCCTGAGTAGCTGGGATTGCAGGTGCATA GAAATCCTGGGTTCAAGTGATTCTTTCACCTCGGCCTCCTGAGTAGCTGGGATTGCAGGTGCATA A G TRIO Ensembl:ENSG00000038382 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs572817522 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77339,RMVar_hsa_circ_94247,RMVar_hsa_circ_93187,RMVar_hsa_circ_107815,RMVar_hsa_circ_230320,RMVar_hsa_circ_230321,RMVar_hsa_circ_230319,RMVar_hsa_circ_230322 3229 RMVar_ID_3229 Human_SNP_ID_222343506 A-to-I Human chr5 + 14234010 14234010 14234010 TGTGGAGACAGGGTGTCACTGTTTCCCAGGCTAGTCTCAAACTCCTGGCCTCAAGTGATCCTCTC TGTGGAGACAGGGTGTCACTGTTTCCCAGGCTCGTCTCAAACTCCTGGCCTCAAGTGATCCTCTC A C TRIO Ensembl:ENSG00000038382 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs372494872 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77339,RMVar_hsa_circ_94247,RMVar_hsa_circ_93187,RMVar_hsa_circ_107815,RMVar_hsa_circ_230320,RMVar_hsa_circ_230321,RMVar_hsa_circ_230319,RMVar_hsa_circ_230322 3230 RMVar_ID_3230 Human_SNP_ID_222386479 A-to-I Human chr5 + 14396649 14396649 14396649 ATGCCACCATGCCCAGCTAATTTTTTTTTTTTAAGTAGAGATGGAGTTTTACCATGTTGGCCAGG ATGCCACCATGCCCAGCTAATTTTTTTTTTTTGAGTAGAGATGGAGTTTTACCATGTTGGCCAGG A G TRIO Ensembl:ENSG00000038382 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1158569818 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_5235,RMVar_hsa_circ_230347,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_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_309426,RMVar_hsa_circ_230388,RMVar_hsa_circ_376395,RMVar_hsa_circ_305427,RMVar_hsa_circ_230395,RMVar_hsa_circ_54021,RMVar_hsa_circ_26772,RMVar_hsa_circ_35473,RMVar_hsa_circ_7035,RMVar_hsa_circ_76844,RMVar_hsa_circ_230398,RMVar_hsa_circ_230400,RMVar_hsa_circ_97857,RMVar_hsa_circ_88005,RMVar_hsa_circ_2594,RMVar_hsa_circ_230402,RMVar_hsa_circ_230403,RMVar_hsa_circ_92629,RMVar_hsa_circ_230405,RMVar_hsa_circ_230410,RMVar_hsa_circ_371387,RMVar_hsa_circ_85947,RMVar_hsa_circ_230409,RMVar_hsa_circ_109202,RMVar_hsa_circ_340222,RMVar_hsa_circ_230412,RMVar_hsa_circ_230413,RMVar_hsa_circ_90102,RMVar_hsa_circ_106280,RMVar_hsa_circ_230415,RMVar_hsa_circ_46429,RMVar_hsa_circ_230416,RMVar_hsa_circ_230414 3231 RMVar_ID_3231 Human_SNP_ID_222403896 A-to-I Human chr5 + 14459609 14459609 14459609 TTTGAATACAAAAATTAGCTGGGTATGGTGGCAGTCGTCTGTAGTTCCAGCTACTTGGGAGGCTG TTTGAATACAAAAATTAGCTGGGTATGGTGGCGGTCGTCTGTAGTTCCAGCTACTTGGGAGGCTG A G TRIO Ensembl:ENSG00000038382 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1458931487 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23313844 RMVar_hsa_circ_256,RMVar_hsa_circ_77339,RMVar_hsa_circ_230321,RMVar_hsa_circ_372445,RMVar_hsa_circ_230335,RMVar_hsa_circ_5235,RMVar_hsa_circ_127203,RMVar_hsa_circ_117880,RMVar_hsa_circ_81706,RMVar_hsa_circ_95836,RMVar_hsa_circ_230361,RMVar_hsa_circ_230362,RMVar_hsa_circ_117747,RMVar_hsa_circ_112284,RMVar_hsa_circ_90350,RMVar_hsa_circ_92081,RMVar_hsa_circ_119636,RMVar_hsa_circ_230372,RMVar_hsa_circ_230374,RMVar_hsa_circ_230375,RMVar_hsa_circ_230373,RMVar_hsa_circ_230370,RMVar_hsa_circ_230371,RMVar_hsa_circ_94977,RMVar_hsa_circ_230387,RMVar_hsa_circ_230386,RMVar_hsa_circ_102885,RMVar_hsa_circ_230388,RMVar_hsa_circ_26772,RMVar_hsa_circ_7035,RMVar_hsa_circ_88005,RMVar_hsa_circ_230403,RMVar_hsa_circ_230410,RMVar_hsa_circ_85947,RMVar_hsa_circ_17551,RMVar_hsa_circ_103203,RMVar_hsa_circ_118975,RMVar_hsa_circ_230418,RMVar_hsa_circ_230419,RMVar_hsa_circ_38364,RMVar_hsa_circ_14583,RMVar_hsa_circ_89089,RMVar_hsa_circ_126504,RMVar_hsa_circ_86070,RMVar_hsa_circ_115905,RMVar_hsa_circ_230422,RMVar_hsa_circ_230423,RMVar_hsa_circ_230421,RMVar_hsa_circ_122760,RMVar_hsa_circ_230424,RMVar_hsa_circ_230425 3232 RMVar_ID_3232 Human_SNP_ID_222408056 A-to-I Human chr5 + 14474955 14474955 14474955 CCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCACGCCTGGCCCAATTCAATTTTA CCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCACGCCTGGCCCAATTCAATTTTA A G TRIO Ensembl:ENSG00000038382 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs140800929 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_256,RMVar_hsa_circ_77339,RMVar_hsa_circ_230321,RMVar_hsa_circ_372445,RMVar_hsa_circ_230335,RMVar_hsa_circ_5235,RMVar_hsa_circ_117880,RMVar_hsa_circ_230361,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_94977,RMVar_hsa_circ_230387,RMVar_hsa_circ_230386,RMVar_hsa_circ_102885,RMVar_hsa_circ_230388,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_118975,RMVar_hsa_circ_230418,RMVar_hsa_circ_230419,RMVar_hsa_circ_38364,RMVar_hsa_circ_89089,RMVar_hsa_circ_86070,RMVar_hsa_circ_2276,RMVar_hsa_circ_6855,RMVar_hsa_circ_115905,RMVar_hsa_circ_230422,RMVar_hsa_circ_230423,RMVar_hsa_circ_230425,RMVar_hsa_circ_344586,RMVar_hsa_circ_79898,RMVar_hsa_circ_230428,RMVar_hsa_circ_25757,RMVar_hsa_circ_34708,RMVar_hsa_circ_7697,RMVar_hsa_circ_113517,RMVar_hsa_circ_230430 3233 RMVar_ID_3233 Human_SNP_ID_222453406 A-to-I Human chr5 - 14639964 14639964 14639964 GACTGCTTGGGACATGCAGGACTTGTATATAAATATATATTGGGAGAAGAGAAGTTCACCTTTAT GACTGCTTGGGACATGCAGGACTTGTATATAAGTATATATTGGGAGAAGAGAAGTTCACCTTTAT T C CCT6P2 Ensembl:ENSG00000250526 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs979353874 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1821620,Human_miRNA_ID_1829773 3234 RMVar_ID_3234 Human_SNP_ID_222470106 A-to-I Human chr5 + 14708970 14708970 14708970 GCTGGAGTGCGATGGCGCGATCTCGGCTCACTACAACCTCTGCCTCCCAGGATCAAGCAAATTCT GCTGGAGTGCGATGGCGCGATCTCGGCTCACTGCAACCTCTGCCTCCCAGGATCAAGCAAATTCT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1422454182 Functional Loss SNV dbSNP153 33..33 33 - - - 3235 RMVar_ID_3235 Human_SNP_ID_222472189 A-to-I Human chr5 + 14715307 14715307 14715307 GCATGCGCCACCACGCCTGGCTAATTTTTTGTATTTAGTAGAGACGGGGTTTCACCATGTTGGTG GCATGCGCCACCACGCCTGGCTAATTTTTTGTGTTTAGTAGAGACGGGGTTTCACCATGTTGGTG A G LOC100130744,LOC100130744:2 RNACentral:URS00008B2E81,RNACentral:URS00007599B4 lincRNA,lincRNA intron,intron GSE100210;GSE99789 HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 29129909,29796672 RNA-Seq:(High) rs1028503553 Functional Loss SNV dbSNP153 33..33 33 - - - 3236 RMVar_ID_3236 Human_SNP_ID_222472190 A-to-I Human chr5 + 14715311 14715309 14715312 GCGCCACCACGCCTGGCTAATTTTTTGTATTTAGTAGAGACGGGGTTTCACCATGTTGGTGAGGC GCGCCACCACGCCTGGCTAATTTTTTGTATT___TAGAGACGGGGTTTCACCATGTTGGTGAGGC TTAG T LOC100130744,LOC100130744:2 RNACentral:URS00008B2E81,RNACentral:URS00007599B4 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1389366312 Functional Loss DEL dbSNP153 32..34 33 - - - 3237 RMVar_ID_3237 Human_SNP_ID_222472213 A-to-I Human chr5 + 14715405 14715405 14715405 CACCTGCCTCGGACTACCAAAGTGCTGGAATTACAGGCATAAGCCACTGCGCCCGGCCCATGGCT CACCTGCCTCGGACTACCAAAGTGCTGGAATTGCAGGCATAAGCCACTGCGCCCGGCCCATGGCT A G LOC100130744,LOC100130744:2 RNACentral:URS00008B2E81,RNACentral:URS00007599B4 lincRNA,lincRNA intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1372910011 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27512687 3238 RMVar_ID_3238 Human_SNP_ID_222489851 A-to-I Human chr5 - 14789037 14789037 14789037 TTTTGTAGAGATGGGATTTCACTATGTTAGCCAGGCTGGTCTCAAACTCCTGGGCTCAGGTGATC TTTTGTAGAGATGGGATTTCACTATGTTAGCCGGGCTGGTCTCAAACTCCTGGGCTCAGGTGATC T C ANKH Ensembl:ENSG00000154122 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1414275321 Functional Loss SNV dbSNP153 33..33 33 - - - 3239 RMVar_ID_3239 Human_SNP_ID_222492147 A-to-I Human chr5 - 14797956 14797956 14797956 GTATCATCACAACAAAGACTCCTTCCAGTGATATTCTTGTCTTTGACTATACAAAACATCCTTCT GTATCATCACAACAAAGACTCCTTCCAGTGATGTTCTTGTCTTTGACTATACAAAACATCCTTCT T C ANKH,RBBP4P1 Ensembl:ENSG00000154122,Ensembl:ENSG00000249485 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1206325359 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_166356 3240 RMVar_ID_3240 Human_SNP_ID_222503610 A-to-I Human chr5 - 14846774 14846774 14846774 TTGGCCAGGCTGGGCTTGAACTCCTGATCCCAAGTAATCCATCCGCCTCAGCCTCCCAAAATATT TTGGCCAGGCTGGGCTTGAACTCCTGATCCCAGGTAATCCATCCGCCTCAGCCTCCCAAAATATT T C ANKH Ensembl:ENSG00000154122 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs573123638 Functional Loss SNV dbSNP153 33..33 33 - - - 3241 RMVar_ID_3241 Human_SNP_ID_222503619 A-to-I Human chr5 - 14846809 14846809 14846809 GTGTGTGTTTTTAGTAGAGACGCAGTTTTACCATGTTGGCCAGGCTGGGCTTGAACTCCTGATCC GTGTGTGTTTTTAGTAGAGACGCAGTTTTACCTTGTTGGCCAGGCTGGGCTTGAACTCCTGATCC T A ANKH Ensembl:ENSG00000154122 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1257557317 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2908783 3242 RMVar_ID_3242 Human_SNP_ID_222503620 A-to-I Human chr5 - 14846809 14846809 14846809 GTGTGTGTTTTTAGTAGAGACGCAGTTTTACCATGTTGGCCAGGCTGGGCTTGAACTCCTGATCC GTGTGTGTTTTTAGTAGAGACGCAGTTTTACCGTGTTGGCCAGGCTGGGCTTGAACTCCTGATCC T C ANKH Ensembl:ENSG00000154122 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1257557317 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2908783 3243 RMVar_ID_3243 Human_SNP_ID_222503945 A-to-I Human chr5 - 14847939 14847939 14847939 GGGGTTTCACCACGTTGGCCAGGCTGGTCTCAAACTCCTGACCTCAAGTTATCCGCCCACCTCAG GGGGTTTCACCACGTTGGCCAGGCTGGTCTCAGACTCCTGACCTCAAGTTATCCGCCCACCTCAG T C ANKH Ensembl:ENSG00000154122 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs191968236 Functional Loss SNV dbSNP153 33..33 33 - - - 3244 RMVar_ID_3244 Human_SNP_ID_222504020 A-to-I Human chr5 - 14848231 14848231 14848231 CACTACCTGATTGGTTGGGTGTGAGCTGAGTTACAAGCCCCACGTTTAAAGGTGGGTGCAGTCAC CACTACCTGATTGGTTGGGTGTGAGCTGAGTTTCAAGCCCCACGTTTAAAGGTGGGTGCAGTCAC T A ANKH Ensembl:ENSG00000154122 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs754221531 Functional Loss SNV dbSNP153 33..33 33 - - - 3245 RMVar_ID_3245 Human_SNP_ID_222507642 A-to-I Human chr5 - 14863994 14863994 14863994 CCCAAGCTGGTCTCGAACTCCTGGGCTTAAGCAATCCTCCCATCTCAGCCTCCCAAACTGTTGGG CCCAAGCTGGTCTCGAACTCCTGGGCTTAAGCCATCCTCCCATCTCAGCCTCCCAAACTGTTGGG T G ANKH Ensembl:ENSG00000154122 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs899494808 Functional Loss SNV dbSNP153 33..33 33 - - - 3246 RMVar_ID_3246 Human_SNP_ID_222507650 A-to-I Human chr5 - 14864022 14864022 14864022 TTTGTAGAGATTGGGTCTTGTGATGTTGCCCAAGCTGGTCTCGAACTCCTGGGCTTAAGCAATCC TTTGTAGAGATTGGGTCTTGTGATGTTGCCCAGGCTGGTCTCGAACTCCTGGGCTTAAGCAATCC T C ANKH Ensembl:ENSG00000154122 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1010119520 Functional Loss SNV dbSNP153 33..33 33 - - - 3247 RMVar_ID_3247 Human_SNP_ID_222508345 A-to-I Human chr5 - 14867081 14867081 14867081 GTGATCTTGGCTCAATGCAGCCACCATTTCCCAGGCTCAAGCGATTCTCCTGCCTCAGTCCCCCG GTGATCTTGGCTCAATGCAGCCACCATTTCCCGGGCTCAAGCGATTCTCCTGCCTCAGTCCCCCG T C ANKH Ensembl:ENSG00000154122 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1364164365 Functional Loss SNV dbSNP153 33..33 33 - - - 3248 RMVar_ID_3248 Human_SNP_ID_468830315 A-to-I Human chr11 - 61003541 61003541 61003541 TTTTGTAGAGACGGGGTTTTCCCATGTTGCCCAGGCTGGTCTCAAATTCCTGAGCTCAAGTGATC TTTTGTAGAGACGGGGTTTTCCCATGTTGCCCGGGCTGGTCTCAAATTCCTGAGCTCAAGTGATC T C HSALNG0084490 RNACentral:URS0000EAC360 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1301257302 Functional Loss SNV dbSNP153 33..33 33 - - - 3249 RMVar_ID_3249 Human_SNP_ID_468863621 A-to-I Human chr11 - 61136277 61136277 61136277 CCCAGCTACAAGGGAGCAAGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCAGGAGGCAGAGGTT CCCAGCTACAAGGGAGCAAGGGAGGCTGAGGCGGGAGAATCGCTTGAACCCAGGAGGCAGAGGTT T C VPS37C Ensembl:ENSG00000167987 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1372862891 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86556,RMVar_hsa_circ_268307,RMVar_hsa_circ_149902,RMVar_hsa_circ_93816,RMVar_hsa_circ_149903,RMVar_hsa_circ_378291,RMVar_hsa_circ_149904 3250 RMVar_ID_3250 Human_SNP_ID_468864562 A-to-I Human chr11 - 61139883 61139883 61139883 TAAAAATTAGCTGGAGGTGGTAACGCACACCTATAGTGCCAGCTATCGGGAGGTTGAGGTGGGAG TAAAAATTAGCTGGAGGTGGTAACGCACACCTGTAGTGCCAGCTATCGGGAGGTTGAGGTGGGAG T C VPS37C Ensembl:ENSG00000167987 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1449520407 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86556,RMVar_hsa_circ_149902 3251 RMVar_ID_3251 Human_SNP_ID_468892603 A-to-I Human chr11 - 61278956 61278956 61278956 CGGCTCACTGCAACGTCTGCCTCCCGGGTTCAAGCGATTCTCCTGCTTCAGCCTCCCGAGTAGCT CGGCTCACTGCAACGTCTGCCTCCCGGGTTCAGGCGATTCTCCTGCTTCAGCCTCCCGAGTAGCT T C VWCE Ensembl:ENSG00000167992 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1486487210 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42977,RMVar_hsa_circ_71930,RMVar_hsa_circ_61496,RMVar_hsa_circ_108774,RMVar_hsa_circ_42728,RMVar_hsa_circ_149923,RMVar_hsa_circ_51950,RMVar_hsa_circ_149930,RMVar_hsa_circ_336063 3252 RMVar_ID_3252 Human_SNP_ID_468902415 A-to-I Human chr11 - 61316749 61316738 61316749 TAGCAAGTTCTTTTGTATTTTTAGCAGGGACAAGGTCTCTCCATTTTGCCCAGGCTGGTCTAGAA TAGCAAGTTCTTTTGTATTTTTAGCAGGGACA___________TTTTGCCCAGGCTGGTCTAGAA ATGGAGAGACCT A DDB1 Ensembl:ENSG00000167986 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1449416743 Functional Loss DEL dbSNP153 33..43 33 - - - RMVar_hsa_circ_1866,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_115494,RMVar_hsa_circ_49773,RMVar_hsa_circ_126979,RMVar_hsa_circ_149945,RMVar_hsa_circ_149948,RMVar_hsa_circ_85587,RMVar_hsa_circ_99207,RMVar_hsa_circ_103004,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_369841,RMVar_hsa_circ_114064,RMVar_hsa_circ_103069,RMVar_hsa_circ_149964,RMVar_hsa_circ_35319,RMVar_hsa_circ_44261,RMVar_hsa_circ_149966,RMVar_hsa_circ_149967,RMVar_hsa_circ_149965,RMVar_hsa_circ_109424,RMVar_hsa_circ_149963,RMVar_hsa_circ_149972,RMVar_hsa_circ_363800,RMVar_hsa_circ_84154,RMVar_hsa_circ_112259,RMVar_hsa_circ_126618,RMVar_hsa_circ_375165,RMVar_hsa_circ_149973,RMVar_hsa_circ_120772,RMVar_hsa_circ_105094,RMVar_hsa_circ_85715,RMVar_hsa_circ_149974,RMVar_hsa_circ_149976,RMVar_hsa_circ_149977,RMVar_hsa_circ_149978,RMVar_hsa_circ_149975,RMVar_hsa_circ_126074,RMVar_hsa_circ_149980,RMVar_hsa_circ_149981,RMVar_hsa_circ_68271,RMVar_hsa_circ_63857,RMVar_hsa_circ_28398 3253 RMVar_ID_3253 Human_SNP_ID_468902418 A-to-I Human chr11 - 61316749 61316749 61316749 TAGCAAGTTCTTTTGTATTTTTAGCAGGGACAAGGTCTCTCCATTTTGCCCAGGCTGGTCTAGAA TAGCAAGTTCTTTTGTATTTTTAGCAGGGACAGGGTCTCTCCATTTTGCCCAGGCTGGTCTAGAA T C DDB1 Ensembl:ENSG00000167986 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1457969030 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1866,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_115494,RMVar_hsa_circ_49773,RMVar_hsa_circ_126979,RMVar_hsa_circ_149945,RMVar_hsa_circ_149948,RMVar_hsa_circ_85587,RMVar_hsa_circ_99207,RMVar_hsa_circ_103004,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_369841,RMVar_hsa_circ_114064,RMVar_hsa_circ_103069,RMVar_hsa_circ_149964,RMVar_hsa_circ_35319,RMVar_hsa_circ_44261,RMVar_hsa_circ_149966,RMVar_hsa_circ_149967,RMVar_hsa_circ_149965,RMVar_hsa_circ_109424,RMVar_hsa_circ_149963,RMVar_hsa_circ_149972,RMVar_hsa_circ_363800,RMVar_hsa_circ_84154,RMVar_hsa_circ_112259,RMVar_hsa_circ_126618,RMVar_hsa_circ_375165,RMVar_hsa_circ_149973,RMVar_hsa_circ_120772,RMVar_hsa_circ_105094,RMVar_hsa_circ_85715,RMVar_hsa_circ_149974,RMVar_hsa_circ_149976,RMVar_hsa_circ_149977,RMVar_hsa_circ_149978,RMVar_hsa_circ_149975,RMVar_hsa_circ_126074,RMVar_hsa_circ_149980,RMVar_hsa_circ_149981,RMVar_hsa_circ_68271,RMVar_hsa_circ_63857,RMVar_hsa_circ_28398 3254 RMVar_ID_3254 Human_SNP_ID_468903197 A-to-I Human chr11 - 61319110 61319108 61319110 CCTCAATATCCTGGGTTCAAGAGATCTTCTCTATGTCAGCCTCCCAGTAGCTGGGACTCCAACCA CCTCAATATCCTGGGTTCAAGAGATCTTCTCT__GTCAGCCTCCCAGTAGCTGGGACTCCAACCA CAT C DDB1 Ensembl:ENSG00000167986 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1240685005 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_1866,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_115494,RMVar_hsa_circ_49773,RMVar_hsa_circ_126979,RMVar_hsa_circ_149945,RMVar_hsa_circ_149948,RMVar_hsa_circ_85587,RMVar_hsa_circ_99207,RMVar_hsa_circ_103004,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_369841,RMVar_hsa_circ_114064,RMVar_hsa_circ_103069,RMVar_hsa_circ_149964,RMVar_hsa_circ_35319,RMVar_hsa_circ_44261,RMVar_hsa_circ_149966,RMVar_hsa_circ_149967,RMVar_hsa_circ_149965,RMVar_hsa_circ_109424,RMVar_hsa_circ_149963,RMVar_hsa_circ_149972,RMVar_hsa_circ_363800,RMVar_hsa_circ_84154,RMVar_hsa_circ_112259,RMVar_hsa_circ_126618,RMVar_hsa_circ_375165,RMVar_hsa_circ_149973,RMVar_hsa_circ_120772,RMVar_hsa_circ_105094,RMVar_hsa_circ_85715,RMVar_hsa_circ_149974,RMVar_hsa_circ_149976,RMVar_hsa_circ_149977,RMVar_hsa_circ_149978,RMVar_hsa_circ_149975,RMVar_hsa_circ_126074,RMVar_hsa_circ_149980,RMVar_hsa_circ_149981,RMVar_hsa_circ_68271,RMVar_hsa_circ_63857,RMVar_hsa_circ_28398 3255 RMVar_ID_3255 Human_SNP_ID_468903198 A-to-I Human chr11 - 61319110 61319110 61319110 CCTCAATATCCTGGGTTCAAGAGATCTTCTCTATGTCAGCCTCCCAGTAGCTGGGACTCCAACCA CCTCAATATCCTGGGTTCAAGAGATCTTCTCTGTGTCAGCCTCCCAGTAGCTGGGACTCCAACCA T C DDB1 Ensembl:ENSG00000167986 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1160302521 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1866,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_115494,RMVar_hsa_circ_49773,RMVar_hsa_circ_126979,RMVar_hsa_circ_149945,RMVar_hsa_circ_149948,RMVar_hsa_circ_85587,RMVar_hsa_circ_99207,RMVar_hsa_circ_103004,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_369841,RMVar_hsa_circ_114064,RMVar_hsa_circ_103069,RMVar_hsa_circ_149964,RMVar_hsa_circ_35319,RMVar_hsa_circ_44261,RMVar_hsa_circ_149966,RMVar_hsa_circ_149967,RMVar_hsa_circ_149965,RMVar_hsa_circ_109424,RMVar_hsa_circ_149963,RMVar_hsa_circ_149972,RMVar_hsa_circ_363800,RMVar_hsa_circ_84154,RMVar_hsa_circ_112259,RMVar_hsa_circ_126618,RMVar_hsa_circ_375165,RMVar_hsa_circ_149973,RMVar_hsa_circ_120772,RMVar_hsa_circ_105094,RMVar_hsa_circ_85715,RMVar_hsa_circ_149974,RMVar_hsa_circ_149976,RMVar_hsa_circ_149977,RMVar_hsa_circ_149978,RMVar_hsa_circ_149975,RMVar_hsa_circ_126074,RMVar_hsa_circ_149980,RMVar_hsa_circ_149981,RMVar_hsa_circ_68271,RMVar_hsa_circ_63857,RMVar_hsa_circ_28398 3256 RMVar_ID_3256 Human_SNP_ID_468903214 A-to-I Human chr11 - 61319170 61319170 61319170 ATAGGGTCTCACTCTGTCACCCAGGCTGGGGTACAGTGGCATGATCACGGCTTACCATAGCCTCA ATAGGGTCTCACTCTGTCACCCAGGCTGGGGTGCAGTGGCATGATCACGGCTTACCATAGCCTCA T C DDB1 Ensembl:ENSG00000167986 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1175980747 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1866,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_115494,RMVar_hsa_circ_49773,RMVar_hsa_circ_126979,RMVar_hsa_circ_149945,RMVar_hsa_circ_149948,RMVar_hsa_circ_85587,RMVar_hsa_circ_99207,RMVar_hsa_circ_103004,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_369841,RMVar_hsa_circ_114064,RMVar_hsa_circ_103069,RMVar_hsa_circ_149964,RMVar_hsa_circ_35319,RMVar_hsa_circ_44261,RMVar_hsa_circ_149966,RMVar_hsa_circ_149967,RMVar_hsa_circ_149965,RMVar_hsa_circ_109424,RMVar_hsa_circ_149963,RMVar_hsa_circ_149972,RMVar_hsa_circ_363800,RMVar_hsa_circ_84154,RMVar_hsa_circ_112259,RMVar_hsa_circ_126618,RMVar_hsa_circ_375165,RMVar_hsa_circ_149973,RMVar_hsa_circ_120772,RMVar_hsa_circ_105094,RMVar_hsa_circ_85715,RMVar_hsa_circ_149974,RMVar_hsa_circ_149976,RMVar_hsa_circ_149977,RMVar_hsa_circ_149978,RMVar_hsa_circ_149975,RMVar_hsa_circ_126074,RMVar_hsa_circ_149980,RMVar_hsa_circ_149981,RMVar_hsa_circ_68271,RMVar_hsa_circ_63857,RMVar_hsa_circ_28398 3257 RMVar_ID_3257 Human_SNP_ID_468905908 A-to-I Human chr11 - 61329454 61329454 61329454 TATTCCACTAGATCGCGATAATAAAGAACTCAAGGCCTTCAACATCCGCCTGGAGGAGCTGCATG TATTCCACTAGATCGCGATAATAAAGAACTCAGGGCCTTCAACATCCGCCTGGAGGAGCTGCATG T C DDB1 Ensembl:ENSG00000167986 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1269028368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1780334,Human_RBP_ID_3376753,Human_RBP_ID_4164813,Human_RBP_ID_5165574,Human_RBP_ID_9362296,Human_RBP_ID_11651688,Human_RBP_ID_26803507 Human_Splice_Rec_1244939,Human_Splice_Rec_1244999,Human_Splice_Rec_1245191,Human_Splice_Rec_1245211 Human_miRNA_ID_109140,Human_miRNA_ID_1966026,Human_miRNA_ID_2361484,Human_miRNA_ID_2977201 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_118249,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_149963,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_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_94839,RMVar_hsa_circ_15314,RMVar_hsa_circ_149987,RMVar_hsa_circ_270991,RMVar_hsa_circ_149989,RMVar_hsa_circ_278082,RMVar_hsa_circ_149992,RMVar_hsa_circ_149990,RMVar_hsa_circ_149991,RMVar_hsa_circ_279650 3258 RMVar_ID_3258 Human_SNP_ID_468906437 A-to-I Human chr11 - 61331465 61331465 61331465 CGTAGGTTGTTTTATGTTATTTTTGTTTGTTTATTTATTTTCTTTGAGACGGGGGTCTCACAGTG CGTAGGTTGTTTTATGTTATTTTTGTTTGTTTGTTTATTTTCTTTGAGACGGGGGTCTCACAGTG T C DDB1 Ensembl:ENSG00000167986 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs766983886 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6081214,Human_RBP_ID_11651723 RMVar_hsa_circ_56241,RMVar_hsa_circ_90525,RMVar_hsa_circ_149933,RMVar_hsa_circ_49773,RMVar_hsa_circ_103004,RMVar_hsa_circ_149956,RMVar_hsa_circ_118249,RMVar_hsa_circ_149962,RMVar_hsa_circ_369841,RMVar_hsa_circ_35319,RMVar_hsa_circ_149963,RMVar_hsa_circ_363800,RMVar_hsa_circ_112259,RMVar_hsa_circ_375165,RMVar_hsa_circ_149973,RMVar_hsa_circ_105094,RMVar_hsa_circ_149974,RMVar_hsa_circ_149975,RMVar_hsa_circ_126074,RMVar_hsa_circ_149981,RMVar_hsa_circ_63857,RMVar_hsa_circ_28398,RMVar_hsa_circ_149986,RMVar_hsa_circ_90530,RMVar_hsa_circ_314781,RMVar_hsa_circ_94839,RMVar_hsa_circ_15314,RMVar_hsa_circ_149990 3259 RMVar_ID_3259 Human_SNP_ID_468912209 A-to-I Human chr11 - 61351805 61351805 61351805 CACTCAAGCGATCTTCCCAATGTAGCCTCCTAAGTAAGCTAGGACTACAGGCATGGACCACCTCA CACTCAAGCGATCTTCCCAATGTAGCCTCCTATGTAAGCTAGGACTACAGGCATGGACCACCTCA T A CYB561A3 Ensembl:ENSG00000162144 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432628264 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150006,RMVar_hsa_circ_107319,RMVar_hsa_circ_320999,RMVar_hsa_circ_368578,RMVar_hsa_circ_314290,RMVar_hsa_circ_150007,RMVar_hsa_circ_150005 3260 RMVar_ID_3260 Human_SNP_ID_468912280 A-to-I Human chr11 - 61352099 61352099 61352099 GGTTTCGATCTTGGCTGTGCCATTTACTAGTTATGCAACTTTGGGCAAGTTAATTTCATTGCTTT GGTTTCGATCTTGGCTGTGCCATTTACTAGTTGTGCAACTTTGGGCAAGTTAATTTCATTGCTTT T C CYB561A3 Ensembl:ENSG00000162144 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs867857874 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150006,RMVar_hsa_circ_107319,RMVar_hsa_circ_320999,RMVar_hsa_circ_368578,RMVar_hsa_circ_314290,RMVar_hsa_circ_150007,RMVar_hsa_circ_150005 3261 RMVar_ID_3261 Human_SNP_ID_468912907 A-to-I Human chr11 - 61354451 61354451 61354451 ATTTTTATTTTTTGTGGACACAGGATCTTGCTATGTTGCCCAGGCTGATCTTGAACTTCTGGCCT ATTTTTATTTTTTGTGGACACAGGATCTTGCTGTGTTGCCCAGGCTGATCTTGAACTTCTGGCCT T C CYB561A3 Ensembl:ENSG00000162144 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1169910071 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11651805 RMVar_hsa_circ_107319,RMVar_hsa_circ_368578,RMVar_hsa_circ_150007,RMVar_hsa_circ_150009,RMVar_hsa_circ_366289 3262 RMVar_ID_3262 Human_SNP_ID_468915756 A-to-I Human chr11 + 61365324 61365324 61365324 AGCTGTGTCGCCAGGCTGGAGTACAGTGGCACAATCTCAGCTCACTGCAACCTCCGCCCCCTGGG AGCTGTGTCGCCAGGCTGGAGTACAGTGGCACGATCTCAGCTCACTGCAACCTCCGCCCCCTGGG A G TMEM138 Ensembl:ENSG00000149483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs543238777 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15418,RMVar_hsa_circ_83840,RMVar_hsa_circ_104601,RMVar_hsa_circ_302128,RMVar_hsa_circ_150011,RMVar_hsa_circ_301024,RMVar_hsa_circ_150012,RMVar_hsa_circ_150013 3263 RMVar_ID_3263 Human_SNP_ID_468915767 A-to-I Human chr11 + 61365364 61365364 61365364 CTCACTGCAACCTCCGCCCCCTGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCTAGTAGCTGGG CTCACTGCAACCTCCGCCCCCTGGGTTCAAGCCATTCTCCTGCCTCAGCCTCCCTAGTAGCTGGG A C TMEM138 Ensembl:ENSG00000149483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs575280520 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15418,RMVar_hsa_circ_83840,RMVar_hsa_circ_104601,RMVar_hsa_circ_302128,RMVar_hsa_circ_150011,RMVar_hsa_circ_301024,RMVar_hsa_circ_150012,RMVar_hsa_circ_150013 3264 RMVar_ID_3264 Human_SNP_ID_468916593 A-to-I Human chr11 + 61368462 61368462 61368462 TGTTAGCCAGGATGGTCTCGATCTCTGACCTCATGATCCGCCTGCCTCTGCCTCCTAAAGTGCTG TGTTAGCCAGGATGGTCTCGATCTCTGACCTCCTGATCCGCCTGCCTCTGCCTCCTAAAGTGCTG A C TMEM138 Ensembl:ENSG00000149483 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1205950047 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11652060 RMVar_hsa_circ_83840,RMVar_hsa_circ_104601,RMVar_hsa_circ_150011,RMVar_hsa_circ_150013,RMVar_hsa_circ_150016,RMVar_hsa_circ_86121,RMVar_hsa_circ_95637,RMVar_hsa_circ_150018 3265 RMVar_ID_3265 Human_SNP_ID_468917248 A-to-I Human chr11 + 61371218 61371218 61371218 CGCCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGACTTCACCATGTTGGCCAGGATGG CGCCACGCCCAGCTAATTTTTGTATTTTTAGTGGAGATGGGACTTCACCATGTTGGCCAGGATGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1258444419 Functional Loss SNV dbSNP153 33..33 33 - - - 3266 RMVar_ID_3266 Human_SNP_ID_468918401 A-to-I Human chr11 + 61376242 61376242 61376242 GTGATGGTGCATGCCTGTAATTCCAGCTACTCAGGAGGCTGAGGTGGGATAATCACTTGAACCCA GTGATGGTGCATGCCTGTAATTCCAGCTACTCCGGAGGCTGAGGTGGGATAATCACTTGAACCCA A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1033989441 Functional Loss SNV dbSNP153 33..33 33 - - - 3267 RMVar_ID_3267 Human_SNP_ID_468924313 A-to-I Human chr11 + 61399994 61399994 61399994 AATTTAAAAACAAGCCAGGTGTGGTGATGCGCACCTGTAGTCCCAGCTATTCAGGAGGCTGTGGC AATTTAAAAACAAGCCAGGTGTGGTGATGCGCGCCTGTAGTCCCAGCTATTCAGGAGGCTGTGGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1268210345 Functional Loss SNV dbSNP153 33..33 33 - - - 3268 RMVar_ID_3268 Human_SNP_ID_468925272 A-to-I Human chr11 - 61404076 61404076 61404076 CACGTATTGACGGTTTATTTCTTTGACCTCCCAGAGGGCTGAACTCTTTCAACTCTGCGCTGCCC CACGTATTGACGGTTTATTTCTTTGACCTCCCGGAGGGCTGAACTCTTTCAACTCTGCGCTGCCC T C CPSF7 Ensembl:ENSG00000149532 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1006170272 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_398419,Human_RBP_ID_751357,Human_RBP_ID_1457940,Human_RBP_ID_1780363,Human_RBP_ID_6081380,Human_RBP_ID_8353464,Human_RBP_ID_8770219,Human_RBP_ID_11652330,Human_RBP_ID_17232503,Human_RBP_ID_17348862,Human_RBP_ID_17465223,Human_RBP_ID_17797774,Human_RBP_ID_24404896,Human_RBP_ID_26409503,Human_RBP_ID_26892148,Human_RBP_ID_27202865,Human_RBP_ID_27412664,Human_RBP_ID_27556920 3269 RMVar_ID_3269 Human_SNP_ID_468926630 A-to-I Human chr11 - 61409791 61409791 61409791 TTTTCTGTTTTTAGTAGAGGCGGGGCTTTACCATACTGGCCAGGTTGGCCTTGAACTCCTGACTT TTTTCTGTTTTTAGTAGAGGCGGGGCTTTACCGTACTGGCCAGGTTGGCCTTGAACTCCTGACTT T C CPSF7 Ensembl:ENSG00000149532 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1336511585 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227754,Human_RBP_ID_11652625 3270 RMVar_ID_3270 Human_SNP_ID_468926639 A-to-I Human chr11 - 61409811 61409811 61409811 GCGTCACCACGCCCGCTAATTTTTCTGTTTTTAGTAGAGGCGGGGCTTTACCATACTGGCCAGGT GCGTCACCACGCCCGCTAATTTTTCTGTTTTTGGTAGAGGCGGGGCTTTACCATACTGGCCAGGT T C CPSF7 Ensembl:ENSG00000149532 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1182762693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11652625 3271 RMVar_ID_3271 Human_SNP_ID_468926689 A-to-I Human chr11 - 61409962 61409962 61409962 AGTGAAACCCTATCTTTTTTTTTTTGAGACAGAGCCTCACTTTGCCGCCCACGCTGGAGTATAGT AGTGAAACCCTATCTTTTTTTTTTTGAGACAGTGCCTCACTTTGCCGCCCACGCTGGAGTATAGT T A CPSF7 Ensembl:ENSG00000149532 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1009927443 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11652632 3272 RMVar_ID_3272 Human_SNP_ID_468926779 A-to-I Human chr11 - 61410312 61410312 61410312 TGGGAGGCCAAGATGGGAGGATTGTTTGAGCCAGGAGTTCGAGACCAGCCTGGGCAACATAGGGA TGGGAGGCCAAGATGGGAGGATTGTTTGAGCCGGGAGTTCGAGACCAGCCTGGGCAACATAGGGA T C CPSF7 Ensembl:ENSG00000149532 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1424469949 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11652651 3273 RMVar_ID_3273 Human_SNP_ID_468926787 A-to-I Human chr11 - 61410359 61410359 61410359 AAGAATTAGGCTTGGCATGATGGCTCACACCTATGATCCCAGCACTTTGGGAGGCCAAGATGGGA AAGAATTAGGCTTGGCATGATGGCTCACACCTGTGATCCCAGCACTTTGGGAGGCCAAGATGGGA T C CPSF7 Ensembl:ENSG00000149532 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs917379721 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24891624 3274 RMVar_ID_3274 Human_SNP_ID_468927274 A-to-I Human chr11 - 61412324 61412324 61412324 GATCACGGCCACTGCACTCCAGCCTGGGCAACAGAGTGAGACTGTCTCAAAAAAAAAAAAAATGA GATCACGGCCACTGCACTCCAGCCTGGGCAACCGAGTGAGACTGTCTCAAAAAAAAAAAAAATGA T G CPSF7 Ensembl:ENSG00000149532 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1457541921 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20775,RMVar_hsa_circ_150021,RMVar_hsa_circ_116705,RMVar_hsa_circ_325034,RMVar_hsa_circ_341262,RMVar_hsa_circ_333194,RMVar_hsa_circ_150023,RMVar_hsa_circ_63858,RMVar_hsa_circ_150024,RMVar_hsa_circ_150022,RMVar_hsa_circ_101153,RMVar_hsa_circ_339353,RMVar_hsa_circ_150026 3275 RMVar_ID_3275 Human_SNP_ID_468927474 A-to-I Human chr11 - 61413124 61413124 61413124 GGCCAGGAATTCAAGACCAGCCTGGTCAACATAGTGAGACCCCATCTCTACAAAAAATTTTTGAA GGCCAGGAATTCAAGACCAGCCTGGTCAACATTGTGAGACCCCATCTCTACAAAAAATTTTTGAA T A CPSF7 Ensembl:ENSG00000149532 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1030892468 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20775,RMVar_hsa_circ_150021,RMVar_hsa_circ_116705,RMVar_hsa_circ_325034,RMVar_hsa_circ_341262,RMVar_hsa_circ_333194,RMVar_hsa_circ_150023,RMVar_hsa_circ_63858,RMVar_hsa_circ_150024,RMVar_hsa_circ_150022,RMVar_hsa_circ_101153,RMVar_hsa_circ_339353,RMVar_hsa_circ_150026 3276 RMVar_ID_3276 Human_SNP_ID_468927545 A-to-I Human chr11 - 61413448 61413448 61413448 TTTTGTATTTTTAGTAGAGACCGGGTTTCACCATTTTGGCCAGGCTGGTCTCGAACTCTGGCTTC TTTTGTATTTTTAGTAGAGACCGGGTTTCACCCTTTTGGCCAGGCTGGTCTCGAACTCTGGCTTC T G CPSF7 Ensembl:ENSG00000149532 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs954997068 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20775,RMVar_hsa_circ_150021,RMVar_hsa_circ_116705,RMVar_hsa_circ_325034,RMVar_hsa_circ_341262,RMVar_hsa_circ_333194,RMVar_hsa_circ_150023,RMVar_hsa_circ_63858,RMVar_hsa_circ_150024,RMVar_hsa_circ_150022,RMVar_hsa_circ_101153,RMVar_hsa_circ_339353,RMVar_hsa_circ_150026 3277 RMVar_ID_3277 Human_SNP_ID_468927772 A-to-I Human chr11 - 61414297 61414297 61414297 CAAAAATAAGCCAGGCATGGTGGCACATGCCTATAGACCCAGCTACTTGGGAGGCTGAGGCACGA CAAAAATAAGCCAGGCATGGTGGCACATGCCTGTAGACCCAGCTACTTGGGAGGCTGAGGCACGA T C CPSF7 Ensembl:ENSG00000149532 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs914002199 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20775,RMVar_hsa_circ_150021,RMVar_hsa_circ_116705,RMVar_hsa_circ_325034,RMVar_hsa_circ_341262,RMVar_hsa_circ_333194,RMVar_hsa_circ_150023,RMVar_hsa_circ_63858,RMVar_hsa_circ_150024,RMVar_hsa_circ_150022,RMVar_hsa_circ_101153,RMVar_hsa_circ_339353,RMVar_hsa_circ_150026 3278 RMVar_ID_3278 Human_SNP_ID_468927807 A-to-I Human chr11 - 61414421 61414421 61414421 TTTTTAGGCCAGGTGCAGTGGCTCATGCCTGTAGTCCCAGCACTTTGGGAGGCCAAGGCCGGTAA TTTTTAGGCCAGGTGCAGTGGCTCATGCCTGTGGTCCCAGCACTTTGGGAGGCCAAGGCCGGTAA T C CPSF7 Ensembl:ENSG00000149532 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs893307374 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20775,RMVar_hsa_circ_150021,RMVar_hsa_circ_116705,RMVar_hsa_circ_325034,RMVar_hsa_circ_341262,RMVar_hsa_circ_333194,RMVar_hsa_circ_150023,RMVar_hsa_circ_63858,RMVar_hsa_circ_150024,RMVar_hsa_circ_150022,RMVar_hsa_circ_101153,RMVar_hsa_circ_339353,RMVar_hsa_circ_150026 3279 RMVar_ID_3279 Human_SNP_ID_468927923 A-to-I Human chr11 - 61414986 61414986 61414986 GTGATCCGCCTGTCTCGGCCTCCCAAAGTGCTAGGATTACAGGTGTGAGCCACCACGTCCAGCCT GTGATCCGCCTGTCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCACGTCCAGCCT T C CPSF7 Ensembl:ENSG00000149532 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs765388731 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20775,RMVar_hsa_circ_150021,RMVar_hsa_circ_116705,RMVar_hsa_circ_325034,RMVar_hsa_circ_341262,RMVar_hsa_circ_333194,RMVar_hsa_circ_150023,RMVar_hsa_circ_63858,RMVar_hsa_circ_150024,RMVar_hsa_circ_150022,RMVar_hsa_circ_101153,RMVar_hsa_circ_339353,RMVar_hsa_circ_150026 3280 RMVar_ID_3280 Human_SNP_ID_468927982 A-to-I Human chr11 - 61415191 61415191 61415191 CCCTGTCGCCCAGGCTGGAGTGCAGTGGTGCAATCTTGGCTCACTACAGCCTCCACCTCCTGGTT CCCTGTCGCCCAGGCTGGAGTGCAGTGGTGCAGTCTTGGCTCACTACAGCCTCCACCTCCTGGTT T C CPSF7 Ensembl:ENSG00000149532 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs573741483 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24891653 RMVar_hsa_circ_20775,RMVar_hsa_circ_150021,RMVar_hsa_circ_116705,RMVar_hsa_circ_325034,RMVar_hsa_circ_341262,RMVar_hsa_circ_333194,RMVar_hsa_circ_150023,RMVar_hsa_circ_63858,RMVar_hsa_circ_150024,RMVar_hsa_circ_150022,RMVar_hsa_circ_101153,RMVar_hsa_circ_339353,RMVar_hsa_circ_150026 3281 RMVar_ID_3281 Human_SNP_ID_468929915 A-to-I Human chr11 - 61422483 61422483 61422483 GTGAAACCCTGTCTCTACAAAAAAAATTTGAAAATTAGCTGGGCATGGTTGCGCATGTCTGTAGT GTGAAACCCTGTCTCTACAAAAAAAATTTGAAGATTAGCTGGGCATGGTTGCGCATGTCTGTAGT T C CPSF7 Ensembl:ENSG00000149532 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1274646336 Functional Loss SNV dbSNP153 33..33 33 - - - 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 3282 RMVar_ID_3282 Human_SNP_ID_468930030 A-to-I Human chr11 - 61422903 61422903 61422903 GTCTGAAACTCTTGGGCTCAAGCAGTTTGCCTATCTCTGCGTCCTAAAGTGCTGGGATACAAGGC GTCTGAAACTCTTGGGCTCAAGCAGTTTGCCTGTCTCTGCGTCCTAAAGTGCTGGGATACAAGGC T C CPSF7 Ensembl:ENSG00000149532 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11230692 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24891726 GWAS_ID_92,GWAS_ID_93,GWAS_ID_94,GWAS_ID_95,GWAS_ID_96 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 3283 RMVar_ID_3283 Human_SNP_ID_468930031 A-to-I Human chr11 - 61422903 61422903 61422903 GTCTGAAACTCTTGGGCTCAAGCAGTTTGCCTATCTCTGCGTCCTAAAGTGCTGGGATACAAGGC GTCTGAAACTCTTGGGCTCAAGCAGTTTGCCTCTCTCTGCGTCCTAAAGTGCTGGGATACAAGGC T G CPSF7 Ensembl:ENSG00000149532 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11230692 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24891726 GWAS_ID_92,GWAS_ID_93,GWAS_ID_94,GWAS_ID_95,GWAS_ID_96 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 3284 RMVar_ID_3284 Human_SNP_ID_468930066 A-to-I Human chr11 - 61423064 61423064 61423064 TCTCACTCTGTTGCCCAGGCTGGCTCACTGCAACCTCAACCTCCCGGGCTCGAGTGATCCTTCTG TCTCACTCTGTTGCCCAGGCTGGCTCACTGCATCCTCAACCTCCCGGGCTCGAGTGATCCTTCTG T A CPSF7 Ensembl:ENSG00000149532 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs897171057 Functional Loss SNV dbSNP153 33..33 33 - - - 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 3285 RMVar_ID_3285 Human_SNP_ID_468930067 A-to-I Human chr11 - 61423064 61423064 61423064 TCTCACTCTGTTGCCCAGGCTGGCTCACTGCAACCTCAACCTCCCGGGCTCGAGTGATCCTTCTG TCTCACTCTGTTGCCCAGGCTGGCTCACTGCAGCCTCAACCTCCCGGGCTCGAGTGATCCTTCTG T C CPSF7 Ensembl:ENSG00000149532 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs897171057 Functional Loss SNV dbSNP153 33..33 33 - - - 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 3286 RMVar_ID_3286 Human_SNP_ID_468931549 A-to-I Human chr11 - 61428321 61428321 61428321 AACAACAACGAGATATGGTGGCTTGTGCCTGTAGTCCCATCTACTCTGGAGAGTGAGGCAAGAGG AACAACAACGAGATATGGTGGCTTGTGCCTGTTGTCCCATCTACTCTGGAGAGTGAGGCAAGAGG T A CPSF7 Ensembl:ENSG00000149532 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1477263625 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11653297,Human_RBP_ID_17559979 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 3287 RMVar_ID_3287 Human_SNP_ID_468931588 A-to-I Human chr11 - 61428436 61428436 61428436 CTTGACTGTAATCTCAGCTGCTCTGGAGCCTGAGATGGGAAGATTACTTAAGACCAGAAGTTCAA CTTGACTGTAATCTCAGCTGCTCTGGAGCCTGGGATGGGAAGATTACTTAAGACCAGAAGTTCAA T C CPSF7 Ensembl:ENSG00000149532 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1279899676 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6081561,Human_RBP_ID_8353511,Human_RBP_ID_11653301 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 3288 RMVar_ID_3288 Human_SNP_ID_468932754 A-to-I Human chr11 + 61431830 61431830 61431830 GCCAATCTCCTGGTTTAGGAGTAGCTGGGACTACAGGCGCCCCCCACCACGCCTGGCTAATTTTT GCCAATCTCCTGGTTTAGGAGTAGCTGGGACTCCAGGCGCCCCCCACCACGCCTGGCTAATTTTT A C AP003108.2,SDHAF2 Ensembl:ENSG00000256591,Ensembl:ENSG00000167985 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs912101792 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11653375 3289 RMVar_ID_3289 Human_SNP_ID_468933791 A-to-I Human chr11 + 61435936 61435936 61435936 CCTGAGGTCGGGAGTTCGAGACCAGCCTGACCAACATAGAGAAACCCTGTCTCTACTAAAAATAC CCTGAGGTCGGGAGTTCGAGACCAGCCTGACCGACATAGAGAAACCCTGTCTCTACTAAAAATAC A G AP003108.2,SDHAF2 Ensembl:ENSG00000256591,Ensembl:ENSG00000167985 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1012789657 Functional Loss SNV dbSNP153 33..33 33 - - - 3290 RMVar_ID_3290 Human_SNP_ID_468933792 A-to-I Human chr11 + 61435941 61435940 61435942 GGTCGGGAGTTCGAGACCAGCCTGACCAACATAGAGAAACCCTGTCTCTACTAAAAATACAAAAT GGTCGGGAGTTCGAGACCAGCCTGACCAACAT__AGAAACCCTGTCTCTACTAAAAATACAAAAT TAG T AP003108.2,SDHAF2 Ensembl:ENSG00000256591,Ensembl:ENSG00000167985 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs917129801 Functional Loss DEL dbSNP153 33..34 33 - - - 3291 RMVar_ID_3291 Human_SNP_ID_468933806 A-to-I Human chr11 + 61436001 61436001 61436001 AAAATCAGACGGGCGTGGTGGGGCATGCCTGTAATCCCAGCTACTCGGGAGGCTGAAGCAGGAGA AAAATCAGACGGGCGTGGTGGGGCATGCCTGTGATCCCAGCTACTCGGGAGGCTGAAGCAGGAGA A G AP003108.2,SDHAF2 Ensembl:ENSG00000256591,Ensembl:ENSG00000167985 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs12792127 Functional Loss SNV dbSNP153 33..33 33 - - - 3292 RMVar_ID_3292 Human_SNP_ID_468933813 A-to-I Human chr11 + 61436028 61436028 61436028 CCTGTAATCCCAGCTACTCGGGAGGCTGAAGCAGGAGAATTGCTTGATCCTGGGAGGCGGAGGTT CCTGTAATCCCAGCTACTCGGGAGGCTGAAGCCGGAGAATTGCTTGATCCTGGGAGGCGGAGGTT A C AP003108.2,SDHAF2 Ensembl:ENSG00000256591,Ensembl:ENSG00000167985 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1432288140 Functional Loss SNV dbSNP153 33..33 33 - - - 3293 RMVar_ID_3293 Human_SNP_ID_468933814 A-to-I Human chr11 + 61436028 61436028 61436028 CCTGTAATCCCAGCTACTCGGGAGGCTGAAGCAGGAGAATTGCTTGATCCTGGGAGGCGGAGGTT CCTGTAATCCCAGCTACTCGGGAGGCTGAAGCGGGAGAATTGCTTGATCCTGGGAGGCGGAGGTT A G AP003108.2,SDHAF2 Ensembl:ENSG00000256591,Ensembl:ENSG00000167985 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1432288140 Functional Loss SNV dbSNP153 33..33 33 - - - 3294 RMVar_ID_3294 Human_SNP_ID_468934701 A-to-I Human chr11 + 61438976 61438975 61438977 TGAGGCAAGAGAATCGCTTGAGCCTGGGAGACAGAGATTGCAGTGAGCTGAGATTGCACCACTGC TGAGGCAAGAGAATCGCTTGAGCCTGGGAGAC__AGATTGCAGTGAGCTGAGATTGCACCACTGC CAG C AP003108.2,SDHAF2 Ensembl:ENSG00000256591,Ensembl:ENSG00000167985 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1204628280 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_108336,RMVar_hsa_circ_284873,RMVar_hsa_circ_150030,RMVar_hsa_circ_150031,RMVar_hsa_circ_150029 3295 RMVar_ID_3295 Human_SNP_ID_468935188 A-to-I Human chr11 + 61440944 61440944 61440944 TCATTCTTGGCTGGATGCAGTGGCTCACACCTATAATTCCAGCGCTTTGGAAGGCTGAGGCAAAG TCATTCTTGGCTGGATGCAGTGGCTCACACCTGTAATTCCAGCGCTTTGGAAGGCTGAGGCAAAG A G AP003108.2,SDHAF2 Ensembl:ENSG00000256591,Ensembl:ENSG00000167985 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893759437 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11653547,Human_RBP_ID_17559981 RMVar_hsa_circ_108336,RMVar_hsa_circ_284873,RMVar_hsa_circ_150030,RMVar_hsa_circ_150031,RMVar_hsa_circ_150029 3296 RMVar_ID_3296 Human_SNP_ID_468935467 A-to-I Human chr11 + 61441958 61441958 61441958 CAGGCTGGAGTGCAGTGGTGCAGTCATGGCTCAGTGCAGGCTCCACCTCCTGGGCTCAAGCGATC CAGGCTGGAGTGCAGTGGTGCAGTCATGGCTCGGTGCAGGCTCCACCTCCTGGGCTCAAGCGATC A G AP003108.2,SDHAF2 Ensembl:ENSG00000256591,Ensembl:ENSG00000167985 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1000387686 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1457994 RMVar_hsa_circ_108336,RMVar_hsa_circ_284873,RMVar_hsa_circ_150030,RMVar_hsa_circ_150031,RMVar_hsa_circ_150029 3297 RMVar_ID_3297 Human_SNP_ID_468937943 A-to-I Human chr11 + 61452072 61452072 61452072 GGTAGATTTCCTTTTTATAGAGACAGGGTCTCACTCTGCCACCCAGGCTGGGGTGCAGTGGTGTG GGTAGATTTCCTTTTTATAGAGACAGGGTCTCTCTCTGCCACCCAGGCTGGGGTGCAGTGGTGTG A T AP003108.2 Ensembl:ENSG00000256591 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1321518618 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8353544 3298 RMVar_ID_3298 Human_SNP_ID_468938613 A-to-I Human chr11 + 61455159 61455159 61455159 ACATGTGGTGGTGGACGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCTTGAA ACATGTGGTGGTGGACGCCTGTAATCCCAGCTCCTCGGGAGGCTGAGGCAGGAGAATTGCTTGAA A C AP003108.2 Ensembl:ENSG00000256591 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1361052982 Functional Loss SNV dbSNP153 33..33 33 - - - 3299 RMVar_ID_3299 Human_SNP_ID_468939683 A-to-I Human chr11 + 61459449 61459449 61459449 GCGATTCTCGTGCCTCAGCCTCCCAAGTAGCTAGGACTACAGATGCCACAACCACGCCCAGCTAA GCGATTCTCGTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGATGCCACAACCACGCCCAGCTAA A G AP003108.2 Ensembl:ENSG00000256591 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1289229699 Functional Loss SNV dbSNP153 33..33 33 - - - 3300 RMVar_ID_3300 Human_SNP_ID_468940242 A-to-I Human chr11 + 61461706 61461706 61461706 CAGGCATGCACCACCACACGCGGGGTTTTACCATGTTGCCCAGGCTGGTCTCGAACCCCTGGGCT CAGGCATGCACCACCACACGCGGGGTTTTACCCTGTTGCCCAGGCTGGTCTCGAACCCCTGGGCT A C AP003108.2 Ensembl:ENSG00000256591 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1028083799 Functional Loss SNV dbSNP153 33..33 33 - - - 3301 RMVar_ID_3301 Human_SNP_ID_468940243 A-to-I Human chr11 + 61461706 61461706 61461706 CAGGCATGCACCACCACACGCGGGGTTTTACCATGTTGCCCAGGCTGGTCTCGAACCCCTGGGCT CAGGCATGCACCACCACACGCGGGGTTTTACCGTGTTGCCCAGGCTGGTCTCGAACCCCTGGGCT A G AP003108.2 Ensembl:ENSG00000256591 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1028083799 Functional Loss SNV dbSNP153 33..33 33 - - - 3302 RMVar_ID_3302 Human_SNP_ID_468941564 A-to-I Human chr11 + 61466694 61466694 61466694 GGGCATGATGATGGGCACCTGTAATGCCAGCTACTCGGGAGGCTGAGTCAGGAGAATTGCTGGAA GGGCATGATGATGGGCACCTGTAATGCCAGCTGCTCGGGAGGCTGAGTCAGGAGAATTGCTGGAA A G AP003108.2 Ensembl:ENSG00000256591 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1323032361 Functional Loss SNV dbSNP153 33..33 33 - - - 3303 RMVar_ID_3303 Human_SNP_ID_468942266 A-to-I Human chr11 + 61469476 61469476 61469476 TCACCTAGGTTGGTGTGTAGTGCTACAGTCTCAGCTCACTGCAACCTCTATCTCCCAGGCTCAAG TCACCTAGGTTGGTGTGTAGTGCTACAGTCTCGGCTCACTGCAACCTCTATCTCCCAGGCTCAAG A G AP003108.2 Ensembl:ENSG00000256591 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1314886918 Functional Loss SNV dbSNP153 33..33 33 - - - 3304 RMVar_ID_3304 Human_SNP_ID_469025861 A-to-I Human chr11 - 61798488 61798488 61798488 CAATAACTCCTAAGAAATCTTAACATTTCGCCAGGCAAGGTGGCTCATCCTGTAATCCCAGCACT CAATAACTCCTAAGAAATCTTAACATTTCGCCGGGCAAGGTGGCTCATCCTGTAATCCCAGCACT T C - - Other Unknown GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs778536288 Functional Loss SNV dbSNP153 33..33 33 - - - 3305 RMVar_ID_3305 Human_SNP_ID_469026065 A-to-I Human chr11 - 61799255 61799255 61799255 TCTTTATTTTTACACTTACTTGTTTTGAGACAAGGTCTGGCTCTATGGCCCAGGCTGGAGTGCAG TCTTTATTTTTACACTTACTTGTTTTGAGACACGGTCTGGCTCTATGGCCCAGGCTGGAGTGCAG T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1435108383 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6081789 3306 RMVar_ID_3306 Human_SNP_ID_469026257 A-to-I Human chr11 - 61800254 61800254 61800254 AGGAGGTCAAGCCTGCAGCGAGCTGAGATCACACCACTGCACTCCAGCCTGGGGTGATAGAACAA AGGAGGTCAAGCCTGCAGCGAGCTGAGATCACGCCACTGCACTCCAGCCTGGGGTGATAGAACAA T C FADS1 Ensembl:ENSG00000149485 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1127959 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11654472 Human_miRNA_ID_282849 RMVar_hsa_circ_85425,RMVar_hsa_circ_118566,RMVar_hsa_circ_103399,RMVar_hsa_circ_113848,RMVar_hsa_circ_102622,RMVar_hsa_circ_150067,RMVar_hsa_circ_150069,RMVar_hsa_circ_150070,RMVar_hsa_circ_150071,RMVar_hsa_circ_150068 3307 RMVar_ID_3307 Human_SNP_ID_469026259 A-to-I Human chr11 - 61800261 61800261 61800261 TGGGCCCAGGAGGTCAAGCCTGCAGCGAGCTGAGATCACACCACTGCACTCCAGCCTGGGGTGAT TGGGCCCAGGAGGTCAAGCCTGCAGCGAGCTGCGATCACACCACTGCACTCCAGCCTGGGGTGAT T G FADS1 Ensembl:ENSG00000149485 Protein coding 3'UTR GSE38233;GSE107867 cultured B-cells;ASD brains,temporal_cortex - 24183664,30559470 RNA-Seq:(High) rs1056720719 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85425,RMVar_hsa_circ_118566,RMVar_hsa_circ_103399,RMVar_hsa_circ_113848,RMVar_hsa_circ_102622,RMVar_hsa_circ_150067,RMVar_hsa_circ_150069,RMVar_hsa_circ_150070,RMVar_hsa_circ_150071,RMVar_hsa_circ_150068 3308 RMVar_ID_3308 Human_SNP_ID_469026382 A-to-I Human chr11 - 61801023 61801023 61801023 TTGTGATTTCTATTGCTGTAGCTAGGTATCTTACTCTGTCCACTCTTGTTCAAGTATCTAACTCT TTGTGATTTCTATTGCTGTAGCTAGGTATCTTTCTCTGTCCACTCTTGTTCAAGTATCTAACTCT T A FADS1 Ensembl:ENSG00000149485 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1339628561 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3376903,Human_RBP_ID_6081820,Human_RBP_ID_17232526,Human_RBP_ID_17348882,Human_RBP_ID_17465246,Human_RBP_ID_19582260,Human_RBP_ID_22380810,Human_RBP_ID_23206950,Human_RBP_ID_26404716,Human_RBP_ID_27412792 RMVar_hsa_circ_85425,RMVar_hsa_circ_118566,RMVar_hsa_circ_103399,RMVar_hsa_circ_113848,RMVar_hsa_circ_102622,RMVar_hsa_circ_150067,RMVar_hsa_circ_150069,RMVar_hsa_circ_150070,RMVar_hsa_circ_150071,RMVar_hsa_circ_150068 3309 RMVar_ID_3309 Human_SNP_ID_469029164 A-to-I Human chr11 - 61813509 61813509 61813509 TTTACAAACCTCTAGCTACAGAAAAGTTCTCCAAGTCTGCACTCGACCCAGGAAGTCCATCTGGC TTTACAAACCTCTAGCTACAGAAAAGTTCTCCGAGTCTGCACTCGACCCAGGAAGTCCATCTGGC T C FADS1 Ensembl:ENSG00000149485 Protein coding intron GSE47997;GSE99789 K562 cells&HepG2 cells;esophageal squamous carcinoma cells,EC109 - 23474544,29796672 RNA-Seq:(High) rs971228754 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17560323,Human_RBP_ID_22569227 Human_Splice_Rec_1246932,Human_Splice_Rec_1246954,Human_Splice_Rec_1246955,Human_Splice_Rec_1246958 3310 RMVar_ID_3310 Human_SNP_ID_469029203 A-to-I Human chr11 - 61813670 61813670 61813670 TGAGCCACCGCGCCCGGCCGGGAGCAGCTTTTATTCCCTTATTTGTCCCTGCCCATGTCCTGCTG TGAGCCACCGCGCCCGGCCGGGAGCAGCTTTTCTTCCCTTATTTGTCCCTGCCCATGTCCTGCTG T G FADS1 Ensembl:ENSG00000149485 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs936918368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17559673 3311 RMVar_ID_3311 Human_SNP_ID_469029372 A-to-I Human chr11 - 61814130 61814130 61814130 ATGAAGCCATGAACCTTCGCGGTGAGTGTTACAGCTCTTACAGGTGGCGTGGACCCAAAGAGTGA ATGAAGCCATGAACCTTCGCGGTGAGTGTTACCGCTCTTACAGGTGGCGTGGACCCAAAGAGTGA T G FADS1 Ensembl:ENSG00000149485 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs889518185 Functional Loss SNV dbSNP153 33..33 33 - - - 3312 RMVar_ID_3312 Human_SNP_ID_469029466 A-to-I Human chr11 - 61814533 61814533 61814533 GGTCTGCAAAGAGTGTTATTCCTTTAAGAGCTATAACAGCGGGAAGGTCCACGGCTCCATTCTTG GGTCTGCAAAGAGTGTTATTCCTTTAAGAGCTGTAACAGCGGGAAGGTCCACGGCTCCATTCTTG T C FADS1 Ensembl:ENSG00000149485 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs568151638 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17560329 3313 RMVar_ID_3313 Human_SNP_ID_469029476 A-to-I Human chr11 - 61814590 61814590 61814590 TGTGGAAGCATTGTTCTTTTGCTCGTCACACTAAACCTTGCTGCTGCTCATTCTTTGGGTCTGCA TGTGGAAGCATTGTTCTTTTGCTCGTCACACTCAACCTTGCTGCTGCTCATTCTTTGGGTCTGCA T G FADS1 Ensembl:ENSG00000149485 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1290139939 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17559675 3314 RMVar_ID_3314 Human_SNP_ID_469029547 A-to-I Human chr11 - 61814828 61814828 61814828 AGAGGTGAAGCCAGCTGGAGTTGATGGGTCGAATGGGGACCTAGAGAACTTTTCTGTATCTAGAG AGAGGTGAAGCCAGCTGGAGTTGATGGGTCGATTGGGGACCTAGAGAACTTTTCTGTATCTAGAG T A FADS1 Ensembl:ENSG00000149485 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs779560344 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1246835 3315 RMVar_ID_3315 Human_SNP_ID_469031165 A-to-I Human chr11 + 61821246 61821240 61821246 AATGAGCTTAAGACCCTAATGCCAGGCCAGGCACAGTGACTCGTGCCTATAATCCCAGTGCTTTG AATGAGCTTAAGACCCTAATGCCAGGC______CAGTGACTCGTGCCTATAATCCCAGTGCTTTG CCAGGCA C FADS2 Ensembl:ENSG00000134824 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1349663621 Functional Loss DEL dbSNP153 28..33 33 - - - 3316 RMVar_ID_3316 Human_SNP_ID_469031828 A-to-I Human chr11 + 61824261 61824261 61824261 AAATTAGCTGGGTGTGGTGGCACATGCCATGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAATTAGCTGGGTGTGGTGGCACATGCCATGTGATCCCAGCTACTCGGGAGGCTGAGGCAGGAGA A G FADS2 Ensembl:ENSG00000134824 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs970534513 Functional Loss SNV dbSNP153 33..33 33 - - - 3317 RMVar_ID_3317 Human_SNP_ID_469037118 A-to-I Human chr11 + 61844759 61844759 61844759 CATCCTGGCTAACACGGTGAAACCCCATCTCCACTAAAAATACAAAAAATTAGCCGGGCGTGGTG CATCCTGGCTAACACGGTGAAACCCCATCTCCGCTAAAAATACAAAAAATTAGCCGGGCGTGGTG A G FADS2 Ensembl:ENSG00000134824 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1267857503 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_330123,RMVar_hsa_circ_376556,RMVar_hsa_circ_41699,RMVar_hsa_circ_150091,RMVar_hsa_circ_81162,RMVar_hsa_circ_150092,RMVar_hsa_circ_113767,RMVar_hsa_circ_150095 3318 RMVar_ID_3318 Human_SNP_ID_469037121 A-to-I Human chr11 + 61844778 61844778 61844778 AAACCCCATCTCCACTAAAAATACAAAAAATTAGCCGGGCGTGGTGGCACACGCCTGCAGTCCCA AAACCCCATCTCCACTAAAAATACAAAAAATTTGCCGGGCGTGGTGGCACACGCCTGCAGTCCCA A T FADS2 Ensembl:ENSG00000134824 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs868411500 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_330123,RMVar_hsa_circ_376556,RMVar_hsa_circ_41699,RMVar_hsa_circ_150091,RMVar_hsa_circ_81162,RMVar_hsa_circ_150092,RMVar_hsa_circ_113767,RMVar_hsa_circ_150095 3319 RMVar_ID_3319 Human_SNP_ID_469038387 A-to-I Human chr11 + 61849528 61849528 61849528 ATCCCTTGAGCTGAGCCCAGGAGGTTGAGGCTACAGTGAGCTATGATCACACCACTGCACTCCAG ATCCCTTGAGCTGAGCCCAGGAGGTTGAGGCTGCAGTGAGCTATGATCACACCACTGCACTCCAG A G FADS2 Ensembl:ENSG00000134824 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1050879827 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24917141 RMVar_hsa_circ_83513,RMVar_hsa_circ_376556,RMVar_hsa_circ_41699,RMVar_hsa_circ_150092,RMVar_hsa_circ_113767,RMVar_hsa_circ_322001,RMVar_hsa_circ_150098 3320 RMVar_ID_3320 Human_SNP_ID_469038466 A-to-I Human chr11 + 61849894 61849894 61849894 TCTGCGAAAAATACAAAAGATTAGCCAGGTGTAGTGGTGTGCGTCTGTGGTCCCAGGTGCAGGGG TCTGCGAAAAATACAAAAGATTAGCCAGGTGTCGTGGTGTGCGTCTGTGGTCCCAGGTGCAGGGG A C FADS2 Ensembl:ENSG00000134824 Protein coding intron GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,31158229,31158229 RNA-Seq:(High) rs923194002 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83513,RMVar_hsa_circ_376556,RMVar_hsa_circ_41699,RMVar_hsa_circ_150092,RMVar_hsa_circ_113767,RMVar_hsa_circ_322001,RMVar_hsa_circ_150098 3321 RMVar_ID_3321 Human_SNP_ID_469038588 A-to-I Human chr11 + 61850299 61850299 61850299 TTGAGACAGAGTCTTACTCTCTTGCCCAGTCTAGAGTGCAGTGGCACGATCTTGGCTCACTGCAA TTGAGACAGAGTCTTACTCTCTTGCCCAGTCTGGAGTGCAGTGGCACGATCTTGGCTCACTGCAA A G FADS2 Ensembl:ENSG00000134824 Protein coding intron GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line - 24183664,31158229 RNA-Seq:(High) rs1166148264 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83513,RMVar_hsa_circ_376556,RMVar_hsa_circ_41699,RMVar_hsa_circ_150092,RMVar_hsa_circ_113767,RMVar_hsa_circ_322001,RMVar_hsa_circ_150098 3322 RMVar_ID_3322 Human_SNP_ID_469040932 A-to-I Human chr11 + 61858362 61858362 61858362 CACCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTTTCCATGTTGGCGAGGCTGG CACCATGCCCAGCTAATTTTTGTATTTTTAGTGGAGATGGGGTTTTTCCATGTTGGCGAGGCTGG A G FADS2 Ensembl:ENSG00000134824 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs545806151 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83513,RMVar_hsa_circ_150098,RMVar_hsa_circ_327634,RMVar_hsa_circ_150100 3323 RMVar_ID_3323 Human_SNP_ID_469041207 A-to-I Human chr11 + 61859317 61859312 61859317 AACCTGAGGTGATCTGCCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCG AACCTGAGGTGATCTGCCCACCTCAGCC_____AAGTGCTGGGATTACAGGCGTGAGCCACCGCG CTCCCA C FADS2 Ensembl:ENSG00000134824 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1482803996 Functional Loss DEL dbSNP153 29..33 33 - - - RMVar_hsa_circ_83513,RMVar_hsa_circ_150098,RMVar_hsa_circ_327634,RMVar_hsa_circ_150100 3324 RMVar_ID_3324 Human_SNP_ID_469041208 A-to-I Human chr11 + 61859317 61859314 61859318 AACCTGAGGTGATCTGCCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCG AACCTGAGGTGATCTGCCCACCTCAGCCTC____AGTGCTGGGATTACAGGCGTGAGCCACCGCG CCCAA C FADS2 Ensembl:ENSG00000134824 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1188644389 Functional Loss DEL dbSNP153 31..34 33 - - - RMVar_hsa_circ_83513,RMVar_hsa_circ_150098,RMVar_hsa_circ_327634,RMVar_hsa_circ_150100 3325 RMVar_ID_3325 Human_SNP_ID_469041578 A-to-I Human chr11 + 61860788 61860788 61860788 ACAAAAAGCTGGGCGTGGTGATGCGCGCCTGTAATCTACCTACTTTGGAGGCTGAGGTAGGAGGA ACAAAAAGCTGGGCGTGGTGATGCGCGCCTGTGATCTACCTACTTTGGAGGCTGAGGTAGGAGGA A G FADS2 Ensembl:ENSG00000134824 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1001247968 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83513,RMVar_hsa_circ_150098,RMVar_hsa_circ_327634,RMVar_hsa_circ_150100 3326 RMVar_ID_3326 Human_SNP_ID_469066641 A-to-I Human chr11 + 61957444 61957444 61957444 GTGGACACCTGTATGCCTACGACTGGATTAGTATCCCACTGGTGTATACACAGGTGAGGACTAGG GTGGACACCTGTATGCCTACGACTGGATTAGTGTCCCACTGGTGTATACACAGGTGAGGACTAGG A G BEST1 Ensembl:ENSG00000167995 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs767552540 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1247212,Human_Splice_Rec_1247213,Human_Splice_Rec_1247230,Human_Splice_Rec_1247231,Human_Splice_Rec_1247244,Human_Splice_Rec_1247245,Human_Splice_Rec_1247260,Human_Splice_Rec_1247261,Human_Splice_Rec_1247278,Human_Splice_Rec_1247279,Human_Splice_Rec_1247294,Human_Splice_Rec_1247295 RMVar_hsa_circ_150128,RMVar_hsa_circ_79130,RMVar_hsa_circ_150130 3327 RMVar_ID_3327 Human_SNP_ID_469201301 A-to-I Human chr11 - 62493151 62493151 62493151 AAAATTAGCTGGGCATGGTGACACACGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGA AAAATTAGCTGGGCATGGTGACACACGCCTGTGATCCCAGCTACTTGGGAGGCTGAGGCAGGAGA T C AHNAK Ensembl:ENSG00000124942 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1397691982 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7291,RMVar_hsa_circ_93703,RMVar_hsa_circ_150144,RMVar_hsa_circ_87555,RMVar_hsa_circ_150145 3328 RMVar_ID_3328 Human_SNP_ID_469207266 A-to-I Human chr11 - 62517953 62517953 62517953 GGAGGTCTTCCAGGCATTGGTGTTCAAGGCCTAGAAGGAAACCTCCAGATGCCTGGAATTAAGTC GGAGGTCTTCCAGGCATTGGTGTTCAAGGCCTGGAAGGAAACCTCCAGATGCCTGGAATTAAGTC T C AHNAK Ensembl:ENSG00000124942 Protein coding intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs760971916 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_30215,Human_RBP_ID_4165853,Human_RBP_ID_8773523 Human_miRNA_ID_1966030,Human_miRNA_ID_2361488,Human_miRNA_ID_2792846 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 3329 RMVar_ID_3329 Human_SNP_ID_469211529 A-to-I Human chr11 - 62528329 62528329 62528329 AAGTGCCAGATGTTGACATCAAAGGACCCAAAATGGACATTGATGCCCCAGATGTGGATGTTCAT AAGTGCCAGATGTTGACATCAAAGGACCCAAAGTGGACATTGATGCCCCAGATGTGGATGTTCAT T C AHNAK Ensembl:ENSG00000124942 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1338852097 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_108814,Human_RBP_ID_8770475 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 3330 RMVar_ID_3330 Human_SNP_ID_469223476 A-to-I Human chr11 - 62570326 62570326 62570326 CAGGCACTGTGTCTAACACCTATAATCCCAGCACTTTGGGAGGCCTAGGCGGGTGGATCACTTGA CAGGCACTGTGTCTAACACCTATAATCCCAGCTCTTTGGGAGGCCTAGGCGGGTGGATCACTTGA T A AP002990.1,EEF1G Ensembl:ENSG00000255508,Ensembl:ENSG00000254772 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs746980416 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150163,RMVar_hsa_circ_94236,RMVar_hsa_circ_96626,RMVar_hsa_circ_87056,RMVar_hsa_circ_77955,RMVar_hsa_circ_150165,RMVar_hsa_circ_150166,RMVar_hsa_circ_150164,RMVar_hsa_circ_80328,RMVar_hsa_circ_78889,RMVar_hsa_circ_105933,RMVar_hsa_circ_150171,RMVar_hsa_circ_150172,RMVar_hsa_circ_122652,RMVar_hsa_circ_81493,RMVar_hsa_circ_150175,RMVar_hsa_circ_150176,RMVar_hsa_circ_121822,RMVar_hsa_circ_150178,RMVar_hsa_circ_150179 3331 RMVar_ID_3331 Human_SNP_ID_469223757 A-to-I Human chr11 - 62571450 62571449 62571450 TTGGGAGTAAGAAATAAAATAGGTTGAAAAAAAGATGCCAAGGATATGTAGGCAATGAGAAGACG TTGGGAGTAAGAAATAAAATAGGTTGAAAAAA_GATGCCAAGGATATGTAGGCAATGAGAAGACG CT C AP002990.1,EEF1G Ensembl:ENSG00000255508,Ensembl:ENSG00000254772 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1381542106 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_11656557 RMVar_hsa_circ_150163,RMVar_hsa_circ_96626,RMVar_hsa_circ_87056,RMVar_hsa_circ_77955,RMVar_hsa_circ_150165,RMVar_hsa_circ_150164,RMVar_hsa_circ_80328,RMVar_hsa_circ_78889,RMVar_hsa_circ_105933,RMVar_hsa_circ_150171,RMVar_hsa_circ_150172,RMVar_hsa_circ_122652,RMVar_hsa_circ_81493,RMVar_hsa_circ_150175,RMVar_hsa_circ_150176,RMVar_hsa_circ_121822,RMVar_hsa_circ_150178,RMVar_hsa_circ_150179,RMVar_hsa_circ_113242,RMVar_hsa_circ_150180 3332 RMVar_ID_3332 Human_SNP_ID_469238124 A-to-I Human chr11 - 62617658 62617658 62617658 ATTGGCCAGGCTGGTCTGGAACTCCAGACCTCAGGTAATTCACCTGCCTCAGCCTCCCAAAGTGT ATTGGCCAGGCTGGTCTGGAACTCCAGACCTCGGGTAATTCACCTGCCTCAGCCTCCCAAAGTGT T C B3GAT3 Ensembl:ENSG00000149541 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs1359652806 Functional Loss SNV dbSNP153 33..33 33 - - - 3333 RMVar_ID_3333 Human_SNP_ID_469238155 A-to-I Human chr11 - 62617794 62617794 62617794 CAGCTCACTCCAACCTCCTCCTTCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCT CAGCTCACTCCAACCTCCTCCTTCCAGGTTCAGGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCT T C B3GAT3 Ensembl:ENSG00000149541 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1466165784 Functional Loss SNV dbSNP153 33..33 33 - - - 3334 RMVar_ID_3334 Human_SNP_ID_469238230 A-to-I Human chr11 - 62618094 62618094 62618094 CGGCTCACTGCAACCTTCGCCTCCCGGGTTCAAGCGATTCTTCTGCCTCAGCCTCCCGAGTAGCT CGGCTCACTGCAACCTTCGCCTCCCGGGTTCATGCGATTCTTCTGCCTCAGCCTCCCGAGTAGCT T A B3GAT3 Ensembl:ENSG00000149541 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs528191404 Functional Loss SNV dbSNP153 33..33 33 - - - 3335 RMVar_ID_3335 Human_SNP_ID_469238491 A-to-I Human chr11 - 62618897 62618897 62618897 CTCACTGCAACCTCCACCTCCCGGATTGAAGCAATTCTCCTGCCTCAGCCCCCCGAGTAGCTGGG CTCACTGCAACCTCCACCTCCCGGATTGAAGCGATTCTCCTGCCTCAGCCCCCCGAGTAGCTGGG T C B3GAT3 Ensembl:ENSG00000149541 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1219787979 Functional Loss SNV dbSNP153 33..33 33 - - - 3336 RMVar_ID_3336 Human_SNP_ID_469241406 A-to-I Human chr11 - 62627566 62627566 62627566 CACCATGCCCGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGTTCAGGCTGA CACCATGCCCGGCTAATTTTTGTATTTTTAGTGGAGACGGGGTTTCACCATGTTGTTCAGGCTGA T C GANAB Ensembl:ENSG00000089597 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1471849999 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87106,RMVar_hsa_circ_91814,RMVar_hsa_circ_150206,RMVar_hsa_circ_374039,RMVar_hsa_circ_150208,RMVar_hsa_circ_109077,RMVar_hsa_circ_150209,RMVar_hsa_circ_92941,RMVar_hsa_circ_113027,RMVar_hsa_circ_150212,RMVar_hsa_circ_103659,RMVar_hsa_circ_150213,RMVar_hsa_circ_150214,RMVar_hsa_circ_150215 3337 RMVar_ID_3337 Human_SNP_ID_469243916 A-to-I Human chr11 - 62635916 62635916 62635916 TAGAAATATGATATCAAGGGGTTGGGCGTGGTAGCTCATGCCTGTAATCCCAGCACTTTGGGAGG TAGAAATATGATATCAAGGGGTTGGGCGTGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGG T C GANAB Ensembl:ENSG00000089597 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs571334404 Functional Loss SNV dbSNP153 33..33 33 - - - 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 3338 RMVar_ID_3338 Human_SNP_ID_469244147 A-to-I Human chr11 - 62636775 62636775 62636775 GGGACTACAGGCGTGCACCACTATGCCTGAGTAGCTGGGACTACAGGCGTGCACCACTATGCCCG GGGACTACAGGCGTGCACCACTATGCCTGAGTGGCTGGGACTACAGGCGTGCACCACTATGCCCG T C GANAB Ensembl:ENSG00000089597 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1262567193 Functional Loss SNV dbSNP153 33..33 33 - - - 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 3339 RMVar_ID_3339 Human_SNP_ID_469245211 A-to-I Human chr11 - 62640046 62640046 62640046 TATTTTTAGTAGAGACAGGGTTTCACCGTGTTAGCCAGGATGGTCTTGATCTCCTGACCTCGTGA TATTTTTAGTAGAGACAGGGTTTCACCGTGTTGGCCAGGATGGTCTTGATCTCCTGACCTCGTGA T C GANAB Ensembl:ENSG00000089597 Protein coding intron GSE38233;GSE99789 cultured B-cells;esophageal squamous carcinoma cells,EC109 - 24183664,29796672 RNA-Seq:(High) rs546401444 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1248496,Human_Splice_Rec_1248642 3340 RMVar_ID_3340 Human_SNP_ID_469245385 A-to-I Human chr11 - 62640411 62640411 62640411 CTCCAGCTCCAGCCTCCCAAGTAGCTGGGACTACAGACACCTGCCACCACGCCCGGCTAATTTTT CTCCAGCTCCAGCCTCCCAAGTAGCTGGGACTGCAGACACCTGCCACCACGCCCGGCTAATTTTT T C GANAB Ensembl:ENSG00000089597 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1313888926 Functional Loss SNV dbSNP153 33..33 33 - - - 3341 RMVar_ID_3341 Human_SNP_ID_469245482 A-to-I Human chr11 - 62640675 62640675 62640675 CTGCCCACCACCACGCCTGGATAATTTTGTGTATTTTTAATAGAGACAGAGTTTCACCGTGTTAG CTGCCCACCACCACGCCTGGATAATTTTGTGTGTTTTTAATAGAGACAGAGTTTCACCGTGTTAG T C GANAB Ensembl:ENSG00000089597 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs528996028 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11657490,Human_RBP_ID_24892578 3342 RMVar_ID_3342 Human_SNP_ID_469245500 A-to-I Human chr11 - 62640721 62640721 62640721 TCACACCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGCTGCCCACCACCACGCCTG TCACACCATTCTCCTGCCTCAGCCTCCCGAGTGGCTGGGACTACAGCTGCCCACCACCACGCCTG T C GANAB Ensembl:ENSG00000089597 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1306832946 Functional Loss SNV dbSNP153 33..33 33 - - - 3343 RMVar_ID_3343 Human_SNP_ID_469245610 A-to-I Human chr11 - 62641182 62641182 62641182 TCAACGCCATGCCCAGCTAATTTTTGTATTTTAAGTAGAGATGGGGTTTCATCATGTTGGCCAGG TCAACGCCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCATCATGTTGGCCAGG T A GANAB Ensembl:ENSG00000089597 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1565110599 Functional Loss SNV dbSNP153 33..33 33 - - - 3344 RMVar_ID_3344 Human_SNP_ID_469245618 A-to-I Human chr11 - 62641222 62641222 62641222 CTCATGCCTCAGCCTCCCGAGTAGCTGTCACTACAGATGCTCAACGCCATGCCCAGCTAATTTTT CTCATGCCTCAGCCTCCCGAGTAGCTGTCACTGCAGATGCTCAACGCCATGCCCAGCTAATTTTT T C GANAB Ensembl:ENSG00000089597 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs963027720 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11657515 3345 RMVar_ID_3345 Human_SNP_ID_469245645 A-to-I Human chr11 - 62641297 62641297 62641297 CTCCATCACCTAGGCTGGAGTGCAGTAGCACAATCTTGGCTCACTGCAACCTCTGCCTCCCGGGT CTCCATCACCTAGGCTGGAGTGCAGTAGCACAGTCTTGGCTCACTGCAACCTCTGCCTCCCGGGT T C GANAB Ensembl:ENSG00000089597 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs542763635 Functional Loss SNV dbSNP153 33..33 33 - - - 3346 RMVar_ID_3346 Human_SNP_ID_469245866 A-to-I Human chr11 - 62641967 62641967 62641967 TGGTCTCGAACTCCTGACCTTGTGATCCGCCCACCCCGGCCTCCCAAAGTGCTGGGTTTACAGGT TGGTCTCGAACTCCTGACCTTGTGATCCGCCCGCCCCGGCCTCCCAAAGTGCTGGGTTTACAGGT T C GANAB Ensembl:ENSG00000089597 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277881258 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11657552,Human_RBP_ID_17559984,Human_RBP_ID_24892600 3347 RMVar_ID_3347 Human_SNP_ID_469245904 A-to-I Human chr11 - 62642055 62642055 62642055 GGCCCCTGCTCCCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATATTGG GGCCCCTGCTCCCATGCCTGGCTAATTTTTGTGTTTTTAGTAGAGATGGGGTTTCACCATATTGG T C GANAB Ensembl:ENSG00000089597 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs915051011 Functional Loss SNV dbSNP153 33..33 33 - - - 3348 RMVar_ID_3348 Human_SNP_ID_469245967 A-to-I Human chr11 - 62642321 62642321 62642321 GGCTGGGCACAGTGGCTGACACTATAATCCCAACACTTTGGGAGGCCAAGATGGGAGGACTGCTT GGCTGGGCACAGTGGCTGACACTATAATCCCAGCACTTTGGGAGGCCAAGATGGGAGGACTGCTT T C GANAB Ensembl:ENSG00000089597 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1390280922 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17560623,Human_RBP_ID_22471626 3349 RMVar_ID_3349 Human_SNP_ID_469246046 A-to-I Human chr11 - 62642573 62642573 62642573 AAAATTAGCTGGGCATGGTGGTGGGCACCTGTAATCCCAGCTGCTCGGGAGGCTGAGGCGGGAGA AAAATTAGCTGGGCATGGTGGTGGGCACCTGTGATCCCAGCTGCTCGGGAGGCTGAGGCGGGAGA T C GANAB Ensembl:ENSG00000089597 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1294429217 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2988 3350 RMVar_ID_3350 Human_SNP_ID_469246065 A-to-I Human chr11 - 62642640 62642640 62642640 ATCTAGGTCAGGAGTTCGATACGAGCCTGGCCAACATGATGAAACCCCGTCTCTACTAAAAATAC ATCTAGGTCAGGAGTTCGATACGAGCCTGGCCGACATGATGAAACCCCGTCTCTACTAAAAATAC T C GANAB Ensembl:ENSG00000089597 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs984519433 Functional Loss SNV dbSNP153 33..33 33 - - - 3351 RMVar_ID_3351 Human_SNP_ID_469246085 A-to-I Human chr11 - 62642705 62642705 62642705 TAGCCAGTGGGGCGCGATGACACAACGCCTGTAATCCCAGCACTGTGGGAGACTGAGACGGGCGG TAGCCAGTGGGGCGCGATGACACAACGCCTGTGATCCCAGCACTGTGGGAGACTGAGACGGGCGG T C GANAB Ensembl:ENSG00000089597 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs184235724 Functional Loss SNV dbSNP153 33..33 33 - - - 3352 RMVar_ID_3352 Human_SNP_ID_469246328 A-to-I Human chr11 - 62643609 62643609 62643609 AGGTGGTGTTTCGCTGTGTCGCCCAGGCTGGAATGCAGTGGCACAACCTTGGCTCACTGCAACCT AGGTGGTGTTTCGCTGTGTCGCCCAGGCTGGAGTGCAGTGGCACAACCTTGGCTCACTGCAACCT T C GANAB Ensembl:ENSG00000089597 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1470327469 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11657600 3353 RMVar_ID_3353 Human_SNP_ID_469246368 A-to-I Human chr11 - 62643732 62643732 62643732 AGCTCACTGCAACCTCTGACTCCCAGGCTCAAACCATTCTCGTTCCTCAGCCTCCCCAGTAGCTG AGCTCACTGCAACCTCTGACTCCCAGGCTCAATCCATTCTCGTTCCTCAGCCTCCCCAGTAGCTG T A GANAB Ensembl:ENSG00000089597 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1252342693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11657603 3354 RMVar_ID_3354 Human_SNP_ID_469246384 A-to-I Human chr11 - 62643785 62643785 62643785 TTGAGACAGAGTCACACTTTGTCACCCAGGCTAGAGTGCAGTGGTGCGATCTCAGCTCACTGCAA TTGAGACAGAGTCACACTTTGTCACCCAGGCTGGAGTGCAGTGGTGCGATCTCAGCTCACTGCAA T C GANAB Ensembl:ENSG00000089597 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs980393781 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11657606,Human_RBP_ID_17560624,Human_RBP_ID_22471627,Human_RBP_ID_23154255 3355 RMVar_ID_3355 Human_SNP_ID_469246646 A-to-I Human chr11 - 62644702 62644702 62644702 TCTCCTGCCTCATCCTCCCGAGTCCTGGGATTACAGACGTGTGCCACCGTGCCCAGCTAATTTTT TCTCCTGCCTCATCCTCCCGAGTCCTGGGATTGCAGACGTGTGCCACCGTGCCCAGCTAATTTTT T C GANAB Ensembl:ENSG00000089597 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1413323506 Functional Loss SNV dbSNP153 33..33 33 - - - 3356 RMVar_ID_3356 Human_SNP_ID_469249072 A-to-I Human chr11 - 62652069 62652069 62652069 GTGATCCACCCTCCTTGGCCTCCCAGAGTGCTAGGATTACAGACGTGAGGCACCTCAGCCAGCCT GTGATCCACCCTCCTTGGCCTCCCAGAGTGCTGGGATTACAGACGTGAGGCACCTCAGCCAGCCT T C INTS5,AP001458.2 Ensembl:ENSG00000185085,Ensembl:ENSG00000255432 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs765741151 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89199,RMVar_hsa_circ_150230 3357 RMVar_ID_3357 Human_SNP_ID_469251909 A-to-I Human chr11 - 62661814 62661814 62661814 TTCCCACGTCGGCCTCCCAAAGTGCTGGGACTACAGGTGTGAGCCACCGTGCCCGGCCACCCCTG TTCCCACGTCGGCCTCCCAAAGTGCTGGGACTGCAGGTGTGAGCCACCGTGCCCGGCCACCCCTG T C AP001458.2 Ensembl:ENSG00000255432 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs377001088 Functional Loss SNV dbSNP153 33..33 33 - - - 3358 RMVar_ID_3358 Human_SNP_ID_469252174 A-to-I Human chr11 - 62662881 62662881 62662881 AGGGATGTCTTTGGGAGGGAAGAAGGTACAGAAGAAAGATTGGAGAAGGGCCTCTCTAGCAGTCA AGGGATGTCTTTGGGAGGGAAGAAGGTACAGATGAAAGATTGGAGAAGGGCCTCTCTAGCAGTCA T A C11orf98,LBHD1,AP001458.2 Ensembl:ENSG00000278615,Ensembl:ENSG00000162194,Ensembl:ENSG00000255432 Protein coding,Protein coding,Protein coding exon,3'UTR,intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs560413045 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1780602,Human_RBP_ID_4167020,Human_RBP_ID_17804616,Human_RBP_ID_21883015 Human_miRNA_ID_2789424,Human_miRNA_ID_2819037 RMVar_hsa_circ_150231,RMVar_hsa_circ_108643,RMVar_hsa_circ_112544,RMVar_hsa_circ_150232 3359 RMVar_ID_3359 Human_SNP_ID_469252175 A-to-I Human chr11 - 62662881 62662881 62662881 AGGGATGTCTTTGGGAGGGAAGAAGGTACAGAAGAAAGATTGGAGAAGGGCCTCTCTAGCAGTCA AGGGATGTCTTTGGGAGGGAAGAAGGTACAGAGGAAAGATTGGAGAAGGGCCTCTCTAGCAGTCA T C C11orf98,LBHD1,AP001458.2 Ensembl:ENSG00000278615,Ensembl:ENSG00000162194,Ensembl:ENSG00000255432 Protein coding,Protein coding,Protein coding exon,3'UTR,intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs560413045 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1780602,Human_RBP_ID_4167020,Human_RBP_ID_17804616,Human_RBP_ID_21883015 Human_miRNA_ID_2789424,Human_miRNA_ID_2819037 RMVar_hsa_circ_150231,RMVar_hsa_circ_108643,RMVar_hsa_circ_112544,RMVar_hsa_circ_150232 3360 RMVar_ID_3360 Human_SNP_ID_469254406 A-to-I Human chr11 - 62668295 62668295 62668295 TTTGTATTTTAGTAGAGATGGGGTTTCACCATATTGCCCAGGCTGGTCTCAAACTCCTGAGCTCA TTTGTATTTTAGTAGAGATGGGGTTTCACCATTTTGCCCAGGCTGGTCTCAAACTCCTGAGCTCA T A LBHD1 Ensembl:ENSG00000162194 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1448629881 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_679,RMVar_hsa_circ_35197 3361 RMVar_ID_3361 Human_SNP_ID_469256479 A-to-I Human chr11 + 62674568 62674568 62674568 AGAATTAGCTGGGTGTGGTGGCACACACCTGCAATCCCAGCTACTCGAGAGGCTGAGGCAGAATT AGAATTAGCTGGGTGTGGTGGCACACACCTGCGATCCCAGCTACTCGAGAGGCTGAGGCAGAATT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1187490805 Functional Loss SNV dbSNP153 33..33 33 - - - 3362 RMVar_ID_3362 Human_SNP_ID_469263627 A-to-I Human chr11 - 62696594 62696594 62696594 TGTGATCACACCACTGCACTCCAGCCTTTGTGACAAGAGCGAGATCCTGTCTCAAAAAAGAAAAG TGTGATCACACCACTGCACTCCAGCCTTTGTGGCAAGAGCGAGATCCTGTCTCAAAAAAGAAAAG T C HNRNPUL2-BSCL2,BSCL2 Ensembl:ENSG00000234857,Ensembl:ENSG00000168000 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs927619339 Functional Loss SNV dbSNP153 33..33 33 - - - 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 3363 RMVar_ID_3363 Human_SNP_ID_469265020 A-to-I Human chr11 - 62701593 62701593 62701593 TCTCTTGACCTTGTGATCTGCCCGCCTCCCAAAGTGCTGGGATTATAGGCGTCAGCCACCACGCC TCTCTTGACCTTGTGATCTGCCCGCCTCCCAAGGTGCTGGGATTATAGGCGTCAGCCACCACGCC T C HNRNPUL2-BSCL2,BSCL2 Ensembl:ENSG00000234857,Ensembl:ENSG00000168000 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005612940 Functional Loss SNV dbSNP153 33..33 33 - - - 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 3364 RMVar_ID_3364 Human_SNP_ID_469265726 A-to-I Human chr11 - 62703857 62703857 62703857 CCTTGGCCTCCCAAAGTGCTGGGATTACAAGCATGAGCCACTGCGCCCGGCCTAGTTCTCTTTTC CCTTGGCCTCCCAAAGTGCTGGGATTACAAGCGTGAGCCACTGCGCCCGGCCTAGTTCTCTTTTC T C HNRNPUL2-BSCL2,BSCL2 Ensembl:ENSG00000234857,Ensembl:ENSG00000168000 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1324678251 Functional Loss SNV dbSNP153 33..33 33 - - - 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 3365 RMVar_ID_3365 Human_SNP_ID_469270455 A-to-I Human chr11 - 62718962 62718962 62718962 AAATTAGTCGGGCATGGTGGTGGGCGCTTGTAATCACAGCTACTCGGGAGGCTGAGGCAGAGAAT AAATTAGTCGGGCATGGTGGTGGGCGCTTGTAGTCACAGCTACTCGGGAGGCTGAGGCAGAGAAT T C HNRNPUL2,HNRNPUL2-BSCL2 Ensembl:ENSG00000214753,Ensembl:ENSG00000234857 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1454698672 Functional Loss SNV dbSNP153 33..33 33 - - - 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 3366 RMVar_ID_3366 Human_SNP_ID_469274868 A-to-I Human chr11 + 62730753 62730753 62730753 GTGGCACCATGCCCTGCTAATTTTGTATTTTTAGTAGAGATGGGATTTCTTCATGTTGGTCAGAC GTGGCACCATGCCCTGCTAATTTTGTATTTTTGGTAGAGATGGGATTTCTTCATGTTGGTCAGAC A G TTC9C Ensembl:ENSG00000162222 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1326088813 Functional Loss SNV dbSNP153 33..33 33 - - - 3367 RMVar_ID_3367 Human_SNP_ID_469274870 A-to-I Human chr11 + 62730756 62730756 62730756 GCACCATGCCCTGCTAATTTTGTATTTTTAGTAGAGATGGGATTTCTTCATGTTGGTCAGACTGG GCACCATGCCCTGCTAATTTTGTATTTTTAGTGGAGATGGGATTTCTTCATGTTGGTCAGACTGG A G TTC9C Ensembl:ENSG00000162222 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs376833842 Functional Loss SNV dbSNP153 33..33 33 - - - 3368 RMVar_ID_3368 Human_SNP_ID_469275051 A-to-I Human chr11 + 62731364 62731364 62731364 CTTCTGTAGCTGGTGCAGTGGCTCACAACTGTAATCCCAACACCTTGGTAGGCCGAGGAGTTCAA CTTCTGTAGCTGGTGCAGTGGCTCACAACTGTGATCCCAACACCTTGGTAGGCCGAGGAGTTCAA A G TTC9C Ensembl:ENSG00000162222 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs144820763 Functional Loss SNV dbSNP153 33..33 33 - - - 3369 RMVar_ID_3369 Human_SNP_ID_469275070 A-to-I Human chr11 + 62731432 62731432 62731432 CAGCCTGGGAAATGTGGCGCAACCCGGTCTCTACAAAAAATACAAAAATTAGCCAGGCATGGTTG CAGCCTGGGAAATGTGGCGCAACCCGGTCTCTGCAAAAAATACAAAAATTAGCCAGGCATGGTTG A G TTC9C Ensembl:ENSG00000162222 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs981411511 Functional Loss SNV dbSNP153 33..33 33 - - - 3370 RMVar_ID_3370 Human_SNP_ID_469275397 A-to-I Human chr11 + 62732452 62732452 62732452 CCAACATGGAGAAACCCATCTGCACTAAAAATACAAAAAAATTAGCCAGGCGTGGTGGTGCATGC CCAACATGGAGAAACCCATCTGCACTAAAAATGCAAAAAAATTAGCCAGGCGTGGTGGTGCATGC A G TTC9C Ensembl:ENSG00000162222 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs12807986 Functional Loss SNV dbSNP153 33..33 33 - - - 3371 RMVar_ID_3371 Human_SNP_ID_469275854 A-to-I Human chr11 + 62734041 62734041 62734041 AATGAGGGGGCTGGGCAGGGTGGTTCACGTCTATAATCCCAGTACATTGGGAGGCTGAGGCCAGC AATGAGGGGGCTGGGCAGGGTGGTTCACGTCTGTAATCCCAGTACATTGGGAGGCTGAGGCCAGC A G TTC9C Ensembl:ENSG00000162222 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs900190127 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150256,RMVar_hsa_circ_333006 3372 RMVar_ID_3372 Human_SNP_ID_469275992 A-to-I Human chr11 + 62734536 62734536 62734536 GTTGAACCTGGAGGTTGCAGTGAGCCAAGATCATGCCACTGCACTCCAGCCTAGCTGATGAGTGA GTTGAACCTGGAGGTTGCAGTGAGCCAAGATCCTGCCACTGCACTCCAGCCTAGCTGATGAGTGA A C TTC9C Ensembl:ENSG00000162222 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1565172018 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150256,RMVar_hsa_circ_333006 3373 RMVar_ID_3373 Human_SNP_ID_469276099 A-to-I Human chr11 + 62734945 62734945 62734945 TGAGACAAAGTTTCACTCTTGTTCCCCAGGCTAGAGTGCAATGGCACGATCTCGGCTCACCGAAA TGAGACAAAGTTTCACTCTTGTTCCCCAGGCTGGAGTGCAATGGCACGATCTCGGCTCACCGAAA A G TTC9C Ensembl:ENSG00000162222 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs977615989 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150256,RMVar_hsa_circ_333006 3374 RMVar_ID_3374 Human_SNP_ID_469277335 A-to-I Human chr11 + 62738889 62738889 62738889 GAGGCCAGCGGATCACCTGAGGTCAGGAGTTCAAGACCAGCCTGACCAACAGGGTAAAACCCTGT GAGGCCAGCGGATCACCTGAGGTCAGGAGTTCGAGACCAGCCTGACCAACAGGGTAAAACCCTGT A G TTC9C Ensembl:ENSG00000162222 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs78357040 Functional Loss SNV dbSNP153 33..33 33 - - - 3375 RMVar_ID_3375 Human_SNP_ID_469277348 A-to-I Human chr11 + 62738937 62738936 62738937 ACAGGGTAAAACCCTGTCTCTACTAAAAATACAAAAATTAGCCTGGCAAGATGACACACGCCTGT ACAGGGTAAAACCCTGTCTCTACTAAAAATAC_AAAATTAGCCTGGCAAGATGACACACGCCTGT CA C TTC9C Ensembl:ENSG00000162222 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1418420235 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_2273359 3376 RMVar_ID_3376 Human_SNP_ID_469277405 A-to-I Human chr11 + 62739174 62739174 62739174 AAAGATGGCCGGGCACGGTGGGTCAGGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGTAG AAAGATGGCCGGGCACGGTGGGTCAGGCCTGTGATCCCAGCACTTTGGGAGGCCGAGGCAGGTAG A G TTC9C Ensembl:ENSG00000162222 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1051603429 Functional Loss SNV dbSNP153 33..33 33 - - - 3377 RMVar_ID_3377 Human_SNP_ID_469277519 A-to-I Human chr11 + 62739646 62739645 62739647 ATATACTAAAGTAACTTTTTGTTTTTTGAGACAGAGTCTCACTCTGTTGCCCAGTCTGGAGTGCA ATATACTAAAGTAACTTTTTGTTTTTTGAGAC__AGTCTCACTCTGTTGCCCAGTCTGGAGTGCA CAG C TTC9C Ensembl:ENSG00000162222 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1428400029 Functional Loss DEL dbSNP153 33..34 33 - - - 3378 RMVar_ID_3378 Human_SNP_ID_469277539 A-to-I Human chr11 + 62739748 62739748 62739748 AGGTTCAAGTGATTCTCGTGTCTGAGCCACCCAAGCAGCTGGGATTACAGGCATGTGCCACCACG AGGTTCAAGTGATTCTCGTGTCTGAGCCACCCCAGCAGCTGGGATTACAGGCATGTGCCACCACG A C TTC9C Ensembl:ENSG00000162222 Protein coding intron GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-Seq:(High) rs879302710 Functional Loss SNV dbSNP153 33..33 33 - - - 3379 RMVar_ID_3379 Human_SNP_ID_469277556 A-to-I Human chr11 + 62739839 62739820 62739839 TTTAGTAGAGACATGGTTTTGCCATGTTGGCCAGGGTGCTCTTGAACTCCTGGCCTCAAGTGATC TTTAGTAGAGACAT___________________GGGTGCTCTTGAACTCCTGGCCTCAAGTGATC TGGTTTTGCCATGTTGGCCA T TTC9C Ensembl:ENSG00000162222 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs946500361 Functional Loss DEL dbSNP153 15..33 33 - - - 3380 RMVar_ID_3380 Human_SNP_ID_469277559 A-to-I Human chr11 + 62739830 62739830 62739830 TATTTCCTTTTTAGTAGAGACATGGTTTTGCCATGTTGGCCAGGGTGCTCTTGAACTCCTGGCCT TATTTCCTTTTTAGTAGAGACATGGTTTTGCCTTGTTGGCCAGGGTGCTCTTGAACTCCTGGCCT A T TTC9C Ensembl:ENSG00000162222 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1257855879 Functional Loss SNV dbSNP153 33..33 33 - - - 3381 RMVar_ID_3381 Human_SNP_ID_469280995 A-to-I Human chr11 - 62751347 62751347 62751347 CACCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCTTGAGCCACCGTGCCTGGCCTCAAGCG CACCCGCCTCAGCCTCCCAAAGTGCTGGGATTGCAGGCTTGAGCCACCGTGCCTGGCCTCAAGCG T C ZBTB3 Ensembl:ENSG00000185670 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1213194183 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89589,RMVar_hsa_circ_150258 3382 RMVar_ID_3382 Human_SNP_ID_469281105 A-to-I Human chr11 - 62751584 62751584 62751584 TCACTGAGGCTGGAGTGCAGTGGCGCAATTTCAGCTCACTGCAACCTCTGCCTCCCAGGTTCAAG TCACTGAGGCTGGAGTGCAGTGGCGCAATTTCGGCTCACTGCAACCTCTGCCTCCCAGGTTCAAG T C ZBTB3 Ensembl:ENSG00000185670 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs531051546 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_110020 RMVar_hsa_circ_89589,RMVar_hsa_circ_150258 3383 RMVar_ID_3383 Human_SNP_ID_469285006 A-to-I Human chr11 + 62763225 62763225 62763225 TGCGATCTTGGCCACTGCCACCTCTGCCTCCTAGGTTCAAGTGATTCTCCTGCCTCGGCCTCCCA TGCGATCTTGGCCACTGCCACCTCTGCCTCCTGGGTTCAAGTGATTCTCCTGCCTCGGCCTCCCA A G POLR2G Ensembl:ENSG00000168002 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1212551577 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26035,RMVar_hsa_circ_101487,RMVar_hsa_circ_150259,RMVar_hsa_circ_120222,RMVar_hsa_circ_150261 3384 RMVar_ID_3384 Human_SNP_ID_469285393 A-to-I Human chr11 + 62764698 62764698 62764698 TGCACCTGTGGTTTCAGCAACTTGGGAGGCTGAGGTGGGAGGATCGCTTGAGCCCAGGAGTTCAA TGCACCTGTGGTTTCAGCAACTTGGGAGGCTGGGGTGGGAGGATCGCTTGAGCCCAGGAGTTCAA A G POLR2G Ensembl:ENSG00000168002 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1364571169 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26035,RMVar_hsa_circ_101487,RMVar_hsa_circ_150259,RMVar_hsa_circ_120222,RMVar_hsa_circ_150261 3385 RMVar_ID_3385 Human_SNP_ID_469285454 A-to-I Human chr11 + 62764908 62764908 62764908 TTGAGACAGAGTCTTGCTCTGTTGCCAGGCTGAAGTGCAATGGTGCAATCTCGGCTCACTGCAAC TTGAGACAGAGTCTTGCTCTGTTGCCAGGCTGGAGTGCAATGGTGCAATCTCGGCTCACTGCAAC A G POLR2G Ensembl:ENSG00000168002 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs186388747 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26035,RMVar_hsa_circ_101487,RMVar_hsa_circ_150259,RMVar_hsa_circ_120222,RMVar_hsa_circ_150261 3386 RMVar_ID_3386 Human_SNP_ID_469287863 A-to-I Human chr11 + 62773722 62773722 62773722 CGCCCGCCTTGGCCTCCGAAAGTGCTGGGATTAGAGGCGTGAGCCACTGGGTCCAGCTACAAATT CGCCCGCCTTGGCCTCCGAAAGTGCTGGGATTGGAGGCGTGAGCCACTGGGTCCAGCTACAAATT A G TAF6L Ensembl:ENSG00000162227 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs184560951 Functional Loss SNV dbSNP153 33..33 33 - - - 3387 RMVar_ID_3387 Human_SNP_ID_469288139 A-to-I Human chr11 + 62774793 62774793 62774793 CAACATGGCGAAATCTTGTTTCTACTAAAAATACAAAAATTAGCTGGGCGTGGTGGCACGTGCCT CAACATGGCGAAATCTTGTTTCTACTAAAAATCCAAAAATTAGCTGGGCGTGGTGGCACGTGCCT A C TAF6L Ensembl:ENSG00000162227 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11231209 Functional Loss SNV dbSNP153 33..33 33 - - - 3388 RMVar_ID_3388 Human_SNP_ID_469288140 A-to-I Human chr11 + 62774793 62774793 62774793 CAACATGGCGAAATCTTGTTTCTACTAAAAATACAAAAATTAGCTGGGCGTGGTGGCACGTGCCT CAACATGGCGAAATCTTGTTTCTACTAAAAATGCAAAAATTAGCTGGGCGTGGTGGCACGTGCCT A G TAF6L Ensembl:ENSG00000162227 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11231209 Functional Loss SNV dbSNP153 33..33 33 - - - 3389 RMVar_ID_3389 Human_SNP_ID_469297612 A-to-I Human chr11 - 62803197 62803197 62803197 ATTCTGCCTCAGTCTCCCGAGTAGCTGGGACTACAGACACCCACCACCACGCCCGGCTAATTTTT ATTCTGCCTCAGTCTCCCGAGTAGCTGGGACTGCAGACACCCACCACCACGCCCGGCTAATTTTT T C NXF1 Ensembl:ENSG00000162231 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs956769624 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108490,RMVar_hsa_circ_37915,RMVar_hsa_circ_150278,RMVar_hsa_circ_118495,RMVar_hsa_circ_150280 3390 RMVar_ID_3390 Human_SNP_ID_469301561 A-to-I Human chr11 - 62816812 62816812 62816812 CGGCTCACTGCAACCTTCGCCTCCCAGGTTCAAGCGATTCTCTTTCCTCAGCCTCCCGAGTACAG CGGCTCACTGCAACCTTCGCCTCCCAGGTTCATGCGATTCTCTTTCCTCAGCCTCCCGAGTACAG T A STX5 Ensembl:ENSG00000162236 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1163990994 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150281,RMVar_hsa_circ_82797,RMVar_hsa_circ_91054,RMVar_hsa_circ_150282 3391 RMVar_ID_3391 Human_SNP_ID_469301572 A-to-I Human chr11 - 62816848 62816848 62816848 GCTGTGTTGCCAGGCTGGAGTGTAGTGGCGCAATCTCGGCTCACTGCAACCTTCGCCTCCCAGGT GCTGTGTTGCCAGGCTGGAGTGTAGTGGCGCAGTCTCGGCTCACTGCAACCTTCGCCTCCCAGGT T C STX5 Ensembl:ENSG00000162236 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1037180658 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17351287 RMVar_hsa_circ_150281,RMVar_hsa_circ_82797,RMVar_hsa_circ_91054,RMVar_hsa_circ_150282 3392 RMVar_ID_3392 Human_SNP_ID_469302431 A-to-I Human chr11 - 62819832 62819832 62819832 AAAAATAGCTGGGCATGGTGACACATGCCTGTAATCCCAACTACTCAGGAGCCAGAGGTGGGAGA AAAAATAGCTGGGCATGGTGACACATGCCTGTGATCCCAACTACTCAGGAGCCAGAGGTGGGAGA T C STX5 Ensembl:ENSG00000162236 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs530523389 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150281,RMVar_hsa_circ_82797,RMVar_hsa_circ_91054,RMVar_hsa_circ_150282 3393 RMVar_ID_3393 Human_SNP_ID_469302819 A-to-I Human chr11 - 62821239 62821239 62821239 CAGTGGCTCGATCTCAGGTCACTGCAGCCTCCACCTTCCAGGTTCAAGTAATTCTCCTGCCTGAG CAGTGGCTCGATCTCAGGTCACTGCAGCCTCCGCCTTCCAGGTTCAAGTAATTCTCCTGCCTGAG T C STX5 Ensembl:ENSG00000162236 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928765191 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150281,RMVar_hsa_circ_82797,RMVar_hsa_circ_91054,RMVar_hsa_circ_150282 3394 RMVar_ID_3394 Human_SNP_ID_469303066 A-to-I Human chr11 - 62822280 62822280 62822280 TGGCTCACTGCAACCTCCACCTCCTAGGTTCAAGTGATTCTCATGCCTCAGTCTCCCGAGTACCT TGGCTCACTGCAACCTCCACCTCCTAGGTTCAGGTGATTCTCATGCCTCAGTCTCCCGAGTACCT T C STX5 Ensembl:ENSG00000162236 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1166787997 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150281,RMVar_hsa_circ_82797,RMVar_hsa_circ_91054,RMVar_hsa_circ_150282 3395 RMVar_ID_3395 Human_SNP_ID_469303311 A-to-I Human chr11 - 62823208 62823206 62823208 ATGGAACCACTGCGCTCCAGTCTGAGTGACAGAGCAAGACCCCATCTCAAAAAAAAAAAAGAAAG ATGGAACCACTGCGCTCCAGTCTGAGTGACAG__CAAGACCCCATCTCAAAAAAAAAAAAGAAAG GCT G STX5 Ensembl:ENSG00000162236 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1246726913 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_150281,RMVar_hsa_circ_82797,RMVar_hsa_circ_91054,RMVar_hsa_circ_150282 3396 RMVar_ID_3396 Human_SNP_ID_469303349 A-to-I Human chr11 - 62823375 62823375 62823375 GAACTCAGGAGTTCAAGACCAGCCTGGGCAACATGGTGAAACCCCATCTCTACAAAAATAAAAAA GAACTCAGGAGTTCAAGACCAGCCTGGGCAACTTGGTGAAACCCCATCTCTACAAAAATAAAAAA T A STX5 Ensembl:ENSG00000162236 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs908666256 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150281,RMVar_hsa_circ_82797,RMVar_hsa_circ_91054,RMVar_hsa_circ_150282 3397 RMVar_ID_3397 Human_SNP_ID_469303350 A-to-I Human chr11 - 62823375 62823375 62823375 GAACTCAGGAGTTCAAGACCAGCCTGGGCAACATGGTGAAACCCCATCTCTACAAAAATAAAAAA GAACTCAGGAGTTCAAGACCAGCCTGGGCAACGTGGTGAAACCCCATCTCTACAAAAATAAAAAA T C STX5 Ensembl:ENSG00000162236 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs908666256 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150281,RMVar_hsa_circ_82797,RMVar_hsa_circ_91054,RMVar_hsa_circ_150282 3398 RMVar_ID_3398 Human_SNP_ID_469303427 A-to-I Human chr11 - 62823719 62823719 62823719 AACAAAGCAAGACCCTGTCTCTACAAAAAAATACAAAAACTAGCTGGGCATGGTGGCATGGGCCT AACAAAGCAAGACCCTGTCTCTACAAAAAAATTCAAAAACTAGCTGGGCATGGTGGCATGGGCCT T A STX5 Ensembl:ENSG00000162236 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1407845351 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150281,RMVar_hsa_circ_82797,RMVar_hsa_circ_91054,RMVar_hsa_circ_150282 3399 RMVar_ID_3399 Human_SNP_ID_469303441 A-to-I Human chr11 - 62823766 62823766 62823766 GAGCAATGCAGATCGCTTGAGTTCAGGAATTCAAGACCAGTTTGGGCAACAAAGCAAGACCCTGT GAGCAATGCAGATCGCTTGAGTTCAGGAATTCGAGACCAGTTTGGGCAACAAAGCAAGACCCTGT T C STX5 Ensembl:ENSG00000162236 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs934239893 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11659994 RMVar_hsa_circ_150281,RMVar_hsa_circ_82797,RMVar_hsa_circ_91054,RMVar_hsa_circ_150282 3400 RMVar_ID_3400 Human_SNP_ID_469304730 A-to-I Human chr11 - 62828243 62828243 62828243 TAGGTGTGGTGGTGTGCCCTGTAGTCCCAGCTACTTGGGAGGCTGAAGTTGGAGGATCACTTGAG TAGGTGTGGTGGTGTGCCCTGTAGTCCCAGCTTCTTGGGAGGCTGAAGTTGGAGGATCACTTGAG T A STX5 Ensembl:ENSG00000162236 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1490064524 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4086,RMVar_hsa_circ_45334 3401 RMVar_ID_3401 Human_SNP_ID_469304793 A-to-I Human chr11 - 62828483 62828483 62828483 TGACCTCGTGATCCGCCTGCCTCAGCTTTCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCAC TGACCTCGTGATCCGCCTGCCTCAGCTTTCCAGAGTGCTGGGATTACAGGCGTGAGCCACTGCAC T C STX5 Ensembl:ENSG00000162236 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1238031382 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4086,RMVar_hsa_circ_45334 3402 RMVar_ID_3402 Human_SNP_ID_469304794 A-to-I Human chr11 - 62828483 62828483 62828483 TGACCTCGTGATCCGCCTGCCTCAGCTTTCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCAC TGACCTCGTGATCCGCCTGCCTCAGCTTTCCACAGTGCTGGGATTACAGGCGTGAGCCACTGCAC T G STX5 Ensembl:ENSG00000162236 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1238031382 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4086,RMVar_hsa_circ_45334 3403 RMVar_ID_3403 Human_SNP_ID_469305339 A-to-I Human chr11 - 62830280 62830280 62830280 AAAATCACTTAGGGTTGGATGTGGTGGCTCATACCTGTAATTCCAGCACTTTGGGAGGCCTAGGC AAAATCACTTAGGGTTGGATGTGGTGGCTCATGCCTGTAATTCCAGCACTTTGGGAGGCCTAGGC T C STX5 Ensembl:ENSG00000162236 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs541550607 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4086,RMVar_hsa_circ_45334 3404 RMVar_ID_3404 Human_SNP_ID_469305382 A-to-I Human chr11 - 62830471 62830471 62830471 TGATGATAGCTCACTTGCAGTCTTGAACTCCTAGACTCAAGGGATCCTCTTTCCTCAGCCTCCTG TGATGATAGCTCACTTGCAGTCTTGAACTCCTCGACTCAAGGGATCCTCTTTCCTCAGCCTCCTG T G STX5 Ensembl:ENSG00000162236 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1440177791 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1249866,Human_Splice_Rec_1249878 RMVar_hsa_circ_4086,RMVar_hsa_circ_45334 3405 RMVar_ID_3405 Human_SNP_ID_469308404 A-to-I Human chr11 - 62840140 62840140 62840140 GCCGGGCGCGGTGGTTTAGTAATACCAGCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGAAGA GCCGGGCGCGGTGGTTTAGTAATACCAGCTGTGATCCCAGCTACTTGGGAGGCTGAGGCAGAAGA T C WDR74 Ensembl:ENSG00000133316 Protein coding 5'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1213716195 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1249925,Human_Splice_Rec_1249969 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 3406 RMVar_ID_3406 Human_SNP_ID_469308683 A-to-I Human chr11 - 62841013 62841011 62841013 CGCCCGGCCTGTTTTGTATTTTTAGTGGAGACAGGGTTTCACAACGTGTTAACCAGGATGGTCTC CGCCCGGCCTGTTTTGTATTTTTAGTGGAGAC__GGTTTCACAACGTGTTAACCAGGATGGTCTC CCT C WDR74 Ensembl:ENSG00000133316 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs201809829 Functional Loss DEL dbSNP153 33..34 33 - - - 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 3407 RMVar_ID_3407 Human_SNP_ID_469308684 A-to-I Human chr11 - 62841013 62841012 62841014 CGCCCGGCCTGTTTTGTATTTTTAGTGGAGACAGGGTTTCACAACGTGTTAACCAGGATGGTCTC CGCCCGGCCTGTTTTGTATTTTTAGTGGAGA__GGGTTTCACAACGTGTTAACCAGGATGGTCTC CTG C WDR74 Ensembl:ENSG00000133316 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs747849513 Functional Loss DEL dbSNP153 32..33 33 - - - 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 3408 RMVar_ID_3408 Human_SNP_ID_469308829 A-to-I Human chr11 - 62841286 62841286 62841286 TTGAGACGTCGTCTTGCTCTGTCGCCCAGGCTAGAGTGCAATGGCATGATCTCAGCTCACTGCAA TTGAGACGTCGTCTTGCTCTGTCGCCCAGGCTGGAGTGCAATGGCATGATCTCAGCTCACTGCAA T C WDR74 Ensembl:ENSG00000133316 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1200814070 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11660310,Human_RBP_ID_23511331 Human_miRNA_ID_1968597,Human_miRNA_ID_2275312,Human_miRNA_ID_2401203,Human_miRNA_ID_2495130,Human_miRNA_ID_2501055,Human_miRNA_ID_3109087,Human_miRNA_ID_3110531 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 3409 RMVar_ID_3409 Human_SNP_ID_469315439 A-to-I Human chr11 + 62857239 62857239 62857239 CGCTTCCCAGGTTCAAGCGATTCTCCTTCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCTCCCG CGCTTCCCAGGTTCAAGCGATTCTCCTTCCTCTGCCTCCTGAGTAGCTGGGATTACAGGCTCCCG A T SLC3A2 Ensembl:ENSG00000168003 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1186722390 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98198,RMVar_hsa_circ_150327,RMVar_hsa_circ_88690,RMVar_hsa_circ_150326 3410 RMVar_ID_3410 Human_SNP_ID_469315525 A-to-I Human chr11 + 62857543 62857543 62857543 TACCGATCTCTACAAAAAAAATAGAAAAAATTAGCCAGGAGCGGTGGTGCATGCCTGTAGCCCCA TACCGATCTCTACAAAAAAAATAGAAAAAATTCGCCAGGAGCGGTGGTGCATGCCTGTAGCCCCA A C SLC3A2 Ensembl:ENSG00000168003 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1324151353 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98198,RMVar_hsa_circ_150327,RMVar_hsa_circ_88690,RMVar_hsa_circ_150326 3411 RMVar_ID_3411 Human_SNP_ID_469315527 A-to-I Human chr11 + 62857547 62857547 62857547 GATCTCTACAAAAAAAATAGAAAAAATTAGCCAGGAGCGGTGGTGCATGCCTGTAGCCCCAGCTG GATCTCTACAAAAAAAATAGAAAAAATTAGCCGGGAGCGGTGGTGCATGCCTGTAGCCCCAGCTG A G SLC3A2 Ensembl:ENSG00000168003 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910877165 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98198,RMVar_hsa_circ_150327,RMVar_hsa_circ_88690,RMVar_hsa_circ_150326 3412 RMVar_ID_3412 Human_SNP_ID_469316118 A-to-I Human chr11 + 62859648 62859648 62859648 CCGGGAGGTGGAAGTTGCAGTGAGCCAAGATCACCCCACTGCACTCCAGCCTGGGGGACAAGAGT CCGGGAGGTGGAAGTTGCAGTGAGCCAAGATCTCCCCACTGCACTCCAGCCTGGGGGACAAGAGT A T SLC3A2 Ensembl:ENSG00000168003 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1263923919 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17560338 RMVar_hsa_circ_98198,RMVar_hsa_circ_150327,RMVar_hsa_circ_88690,RMVar_hsa_circ_150326 3413 RMVar_ID_3413 Human_SNP_ID_469317519 A-to-I Human chr11 + 62865397 62865397 62865397 CAATGTGGCGAAACCCCATCTCTACTAAAAATACAAAAATTAGCTGGGCATGGTGGCGTGTGCCC CAATGTGGCGAAACCCCATCTCTACTAAAAATCCAAAAATTAGCTGGGCATGGTGGCGTGTGCCC A C SLC3A2 Ensembl:ENSG00000168003 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs904773498 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98198,RMVar_hsa_circ_150327,RMVar_hsa_circ_88690,RMVar_hsa_circ_150326 3414 RMVar_ID_3414 Human_SNP_ID_469317904 A-to-I Human chr11 + 62866670 62866670 62866670 CGCCCTCCGCAGCCTCCCAAAGTGCTGAGATTACAAGGTGAGCCACCGCATCTGGCCCTGCTTTT CGCCCTCCGCAGCCTCCCAAAGTGCTGAGATTGCAAGGTGAGCCACCGCATCTGGCCCTGCTTTT A G SLC3A2 Ensembl:ENSG00000168003 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs980109466 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11660881 RMVar_hsa_circ_98198,RMVar_hsa_circ_150327,RMVar_hsa_circ_88690,RMVar_hsa_circ_150326 3415 RMVar_ID_3415 Human_SNP_ID_469318280 A-to-I Human chr11 + 62868096 62868096 62868096 GCCTCCTGCCACCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACAGTGTGGT GCCTCCTGCCACCATGCCCAGCTAATTTTTGTGTTTTTAGTAGAGACGGGGTTTCACAGTGTGGT A G SLC3A2 Ensembl:ENSG00000168003 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs989028714 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11660923 RMVar_hsa_circ_98198,RMVar_hsa_circ_150327,RMVar_hsa_circ_88690,RMVar_hsa_circ_150326 3416 RMVar_ID_3416 Human_SNP_ID_469318281 A-to-I Human chr11 + 62868096 62868096 62868096 GCCTCCTGCCACCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACAGTGTGGT GCCTCCTGCCACCATGCCCAGCTAATTTTTGTTTTTTTAGTAGAGACGGGGTTTCACAGTGTGGT A T SLC3A2 Ensembl:ENSG00000168003 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs989028714 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11660923 RMVar_hsa_circ_98198,RMVar_hsa_circ_150327,RMVar_hsa_circ_88690,RMVar_hsa_circ_150326 3417 RMVar_ID_3417 Human_SNP_ID_469318531 A-to-I Human chr11 + 62869073 62869073 62869073 GGCTTGCACCACCACGCCCCGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGG GGCTTGCACCACCACGCCCCGCTAATTTTTGTGTTTTTAGTAGAGACAGGGTTTCACCATGTTGG A G SLC3A2 Ensembl:ENSG00000168003 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1009175415 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98198,RMVar_hsa_circ_150327,RMVar_hsa_circ_88690,RMVar_hsa_circ_150326 3418 RMVar_ID_3418 Human_SNP_ID_469319542 A-to-I Human chr11 + 62872122 62872122 62872122 TATTTTTAGTAGAGACGGGGTTTCACCATGTTAGCCAGGATGGTCTCGATCTCCTGACCTTGTGA TATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGATGGTCTCGATCTCCTGACCTTGTGA A G SLC3A2 Ensembl:ENSG00000168003 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs942217180 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150327,RMVar_hsa_circ_88690,RMVar_hsa_circ_126206,RMVar_hsa_circ_150331,RMVar_hsa_circ_79749,RMVar_hsa_circ_150330 3419 RMVar_ID_3419 Human_SNP_ID_469319621 A-to-I Human chr11 + 62872459 62872458 62872459 ATTGCTTAAGCTGAGGAAGTCAAGGCTGTAGTAAGCCAAGATCACATTACTGCACTCCAGCCTGG ATTGCTTAAGCTGAGGAAGTCAAGGCTGTAGT_AGCCAAGATCACATTACTGCACTCCAGCCTGG TA T SLC3A2 Ensembl:ENSG00000168003 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1369776409 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_23305113 RMVar_hsa_circ_150327,RMVar_hsa_circ_88690,RMVar_hsa_circ_126206,RMVar_hsa_circ_150331,RMVar_hsa_circ_79749,RMVar_hsa_circ_150330 3420 RMVar_ID_3420 Human_SNP_ID_469319761 A-to-I Human chr11 + 62873121 62873121 62873121 TCAGCTTACTGCACCCTCAACTTCCCAGGCTCAAGTGATACCTCCCACCTCAGCCTCCCGAGTAG TCAGCTTACTGCACCCTCAACTTCCCAGGCTCGAGTGATACCTCCCACCTCAGCCTCCCGAGTAG A G SLC3A2 Ensembl:ENSG00000168003 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs116762262 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150327,RMVar_hsa_circ_88690,RMVar_hsa_circ_126206,RMVar_hsa_circ_150331,RMVar_hsa_circ_79749,RMVar_hsa_circ_150330 3421 RMVar_ID_3421 Human_SNP_ID_469319793 A-to-I Human chr11 + 62873233 62873233 62873233 TTTTGTGGCCGGGCCTGGTGGCTCACGTCTGTAATCCTAGCATTTTGGGAGGCCAAGTCGGGCAG TTTTGTGGCCGGGCCTGGTGGCTCACGTCTGTGATCCTAGCATTTTGGGAGGCCAAGTCGGGCAG A G SLC3A2 Ensembl:ENSG00000168003 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1331932567 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226946 RMVar_hsa_circ_150327,RMVar_hsa_circ_88690,RMVar_hsa_circ_126206,RMVar_hsa_circ_150331,RMVar_hsa_circ_79749,RMVar_hsa_circ_150330 3422 RMVar_ID_3422 Human_SNP_ID_469319799 A-to-I Human chr11 + 62873264 62873264 62873264 TAATCCTAGCATTTTGGGAGGCCAAGTCGGGCAGATCATGAGGTCAGGAGTTCGAGAACAGCCTG TAATCCTAGCATTTTGGGAGGCCAAGTCGGGCGGATCATGAGGTCAGGAGTTCGAGAACAGCCTG A G SLC3A2 Ensembl:ENSG00000168003 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs541013392 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150327,RMVar_hsa_circ_88690,RMVar_hsa_circ_126206,RMVar_hsa_circ_150331,RMVar_hsa_circ_79749,RMVar_hsa_circ_150330 3423 RMVar_ID_3423 Human_SNP_ID_469320332 A-to-I Human chr11 + 62875361 62875361 62875361 GAGATCAGGAGATCAAGACCATCCTGGCTAACATGGTGAAACCCCGTCTCTACTAAAAATACACA GAGATCAGGAGATCAAGACCATCCTGGCTAACCTGGTGAAACCCCGTCTCTACTAAAAATACACA A C SLC3A2 Ensembl:ENSG00000168003 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs371619271 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150327,RMVar_hsa_circ_88690,RMVar_hsa_circ_126206,RMVar_hsa_circ_150331,RMVar_hsa_circ_79749,RMVar_hsa_circ_150330 3424 RMVar_ID_3424 Human_SNP_ID_469320333 A-to-I Human chr11 + 62875361 62875361 62875361 GAGATCAGGAGATCAAGACCATCCTGGCTAACATGGTGAAACCCCGTCTCTACTAAAAATACACA GAGATCAGGAGATCAAGACCATCCTGGCTAACGTGGTGAAACCCCGTCTCTACTAAAAATACACA A G SLC3A2 Ensembl:ENSG00000168003 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs371619271 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150327,RMVar_hsa_circ_88690,RMVar_hsa_circ_126206,RMVar_hsa_circ_150331,RMVar_hsa_circ_79749,RMVar_hsa_circ_150330 3425 RMVar_ID_3425 Human_SNP_ID_469320453 A-to-I Human chr11 + 62875819 62875819 62875819 AAACTCCTGACCTCAGGTGATCCGCCCGCCTCAGCCTCTCAAAGTGCTGGGATTGCAGGCATGAG AAACTCCTGACCTCAGGTGATCCGCCCGCCTCGGCCTCTCAAAGTGCTGGGATTGCAGGCATGAG A G SLC3A2 Ensembl:ENSG00000168003 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1195636831 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150327,RMVar_hsa_circ_88690,RMVar_hsa_circ_126206,RMVar_hsa_circ_150331,RMVar_hsa_circ_79749,RMVar_hsa_circ_150330 3426 RMVar_ID_3426 Human_SNP_ID_469320459 A-to-I Human chr11 + 62875847 62875847 62875847 CCTCAGCCTCTCAAAGTGCTGGGATTGCAGGCATGAGCCACTGCGCCCAGCCTGTTTGTTTGTTT CCTCAGCCTCTCAAAGTGCTGGGATTGCAGGCGTGAGCCACTGCGCCCAGCCTGTTTGTTTGTTT A G SLC3A2 Ensembl:ENSG00000168003 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1005850716 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150327,RMVar_hsa_circ_88690,RMVar_hsa_circ_126206,RMVar_hsa_circ_150331,RMVar_hsa_circ_79749,RMVar_hsa_circ_150330 3427 RMVar_ID_3427 Human_SNP_ID_469320644 A-to-I Human chr11 + 62876807 62876807 62876807 TATTTTTAGTAGAAACGGGGTTTCACCATGTTAGCCAGGCTGATATTGAATTCCTGACCTCAATT TATTTTTAGTAGAAACGGGGTTTCACCATGTTGGCCAGGCTGATATTGAATTCCTGACCTCAATT A G SLC3A2 Ensembl:ENSG00000168003 Protein coding intron GSE38233;GSE56152;GSE100210 cultured B-cells;embryonic stem cells,wild type;HepG2 cell line - 24183664,25708366,29129909 RNA-Seq:(High) rs1431904822 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11661079 Human_Splice_Rec_1250722,Human_Splice_Rec_1250723,Human_Splice_Rec_1250782,Human_Splice_Rec_1250783 RMVar_hsa_circ_150327,RMVar_hsa_circ_88690,RMVar_hsa_circ_126206,RMVar_hsa_circ_150331,RMVar_hsa_circ_79749,RMVar_hsa_circ_150330 3428 RMVar_ID_3428 Human_SNP_ID_469320738 A-to-I Human chr11 + 62877114 62877114 62877114 AGATAGTCTTGCTGTGTTGTCCAGGTTGCAGTACAGTGGTGCGATCTGGGCTCACTGCAACCTCT AGATAGTCTTGCTGTGTTGTCCAGGTTGCAGTGCAGTGGTGCGATCTGGGCTCACTGCAACCTCT A G SLC3A2 Ensembl:ENSG00000168003 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1171918239 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150327,RMVar_hsa_circ_88690,RMVar_hsa_circ_126206,RMVar_hsa_circ_150331,RMVar_hsa_circ_79749,RMVar_hsa_circ_150330 3429 RMVar_ID_3429 Human_SNP_ID_469320767 A-to-I Human chr11 + 62877241 62877241 62877241 CACCACCACGCCTGGCTAATTTTTGTATTTTTAGTAGAGACAGCGTTTCACCATGTTGGCCAGGC CACCACCACGCCTGGCTAATTTTTGTATTTTTGGTAGAGACAGCGTTTCACCATGTTGGCCAGGC A G SLC3A2 Ensembl:ENSG00000168003 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs557828370 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150327,RMVar_hsa_circ_88690,RMVar_hsa_circ_126206,RMVar_hsa_circ_150331,RMVar_hsa_circ_79749,RMVar_hsa_circ_150330 3430 RMVar_ID_3430 Human_SNP_ID_469321211 A-to-I Human chr11 + 62879104 62879104 62879104 CTGTTAGTTTTTTTGAGGCAGAGTCTTGCTCTATCACCCAGACTGGAGTGCAGTGGCCCATTCTT CTGTTAGTTTTTTTGAGGCAGAGTCTTGCTCTGTCACCCAGACTGGAGTGCAGTGGCCCATTCTT A G SLC3A2 Ensembl:ENSG00000168003 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs147598455 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150327,RMVar_hsa_circ_88690,RMVar_hsa_circ_126206,RMVar_hsa_circ_150331,RMVar_hsa_circ_79749,RMVar_hsa_circ_150330 3431 RMVar_ID_3431 Human_SNP_ID_469323439 A-to-I Human chr11 + 62886613 62886613 62886613 ATGCCCAGCTGATCTTTTTTTTTTTTGGAGACAGGTTCTTGCTCTGTTGATCTGGCTGGATTGCA ATGCCCAGCTGATCTTTTTTTTTTTTGGAGACGGGTTCTTGCTCTGTTGATCTGGCTGGATTGCA A G SLC3A2 Ensembl:ENSG00000168003 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277110326 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6083219,Human_RBP_ID_11661360 RMVar_hsa_circ_150334,RMVar_hsa_circ_79749,RMVar_hsa_circ_150330,RMVar_hsa_circ_338474,RMVar_hsa_circ_301056,RMVar_hsa_circ_32370,RMVar_hsa_circ_15597,RMVar_hsa_circ_374378,RMVar_hsa_circ_150342,RMVar_hsa_circ_17039 3432 RMVar_ID_3432 Human_SNP_ID_469323458 A-to-I Human chr11 + 62886707 62886707 62886707 TGCCTCTTGGGTTCAAGTGATACTCCTGCCTCAGCTTCCCAAGTAGCTGGGAATACAGGTGGTCT TGCCTCTTGGGTTCAAGTGATACTCCTGCCTCGGCTTCCCAAGTAGCTGGGAATACAGGTGGTCT A G SLC3A2 Ensembl:ENSG00000168003 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs566474529 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150334,RMVar_hsa_circ_79749,RMVar_hsa_circ_150330,RMVar_hsa_circ_338474,RMVar_hsa_circ_301056,RMVar_hsa_circ_32370,RMVar_hsa_circ_15597,RMVar_hsa_circ_374378,RMVar_hsa_circ_150342,RMVar_hsa_circ_17039 3433 RMVar_ID_3433 Human_SNP_ID_469323665 A-to-I Human chr11 + 62887582 62887582 62887582 AAAAAATTAGCTGGGTGTGGTGGTGCACACCTATGGTCAGCTACTGGGGAGGCTGAGGCAGGAGA AAAAAATTAGCTGGGTGTGGTGGTGCACACCTGTGGTCAGCTACTGGGGAGGCTGAGGCAGGAGA A G SLC3A2 Ensembl:ENSG00000168003 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs985720876 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150334,RMVar_hsa_circ_79749,RMVar_hsa_circ_150330,RMVar_hsa_circ_338474,RMVar_hsa_circ_301056,RMVar_hsa_circ_32370,RMVar_hsa_circ_15597,RMVar_hsa_circ_374378,RMVar_hsa_circ_150342,RMVar_hsa_circ_17039 3434 RMVar_ID_3434 Human_SNP_ID_469323771 A-to-I Human chr11 + 62887938 62887938 62887938 CCTCAGCCTCCCCAGTATCTGGGACTATAGGGATGTAACACTACACCCAGCTAATTTTTAAAAAT CCTCAGCCTCCCCAGTATCTGGGACTATAGGGGTGTAACACTACACCCAGCTAATTTTTAAAAAT A G SLC3A2 Ensembl:ENSG00000168003 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1454767458 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150334,RMVar_hsa_circ_79749,RMVar_hsa_circ_150330,RMVar_hsa_circ_338474,RMVar_hsa_circ_301056,RMVar_hsa_circ_32370,RMVar_hsa_circ_15597,RMVar_hsa_circ_374378,RMVar_hsa_circ_150342,RMVar_hsa_circ_17039 3435 RMVar_ID_3435 Human_SNP_ID_469517920 A-to-I Human chr11 - 63586045 63586043 63586045 GCCTGGCTGATTTTTGTATTTTTTGTAGAGACAGGGTCTCACTTTGTTGTCTGGGCTGGTCTTAA GCCTGGCTGATTTTTGTATTTTTTGTAGAGAC__GGTCTCACTTTGTTGTCTGGGCTGGTCTTAA CCT C PLAAT3 Ensembl:ENSG00000176485 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1313651617 Functional Loss DEL dbSNP153 33..34 33 - - - 3436 RMVar_ID_3436 Human_SNP_ID_469517934 A-to-I Human chr11 - 63586095 63586095 63586095 ACACACACACACACACCCAAGTAGCTGAGACTATGGGTGCACATCACCATGCCTGGCTGATTTTT ACACACACACACACACCCAAGTAGCTGAGACTGTGGGTGCACATCACCATGCCTGGCTGATTTTT T C PLAAT3 Ensembl:ENSG00000176485 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs867694821 Functional Loss SNV dbSNP153 33..33 33 - - - 3437 RMVar_ID_3437 Human_SNP_ID_469530094 A-to-I Human chr11 - 63632187 63632187 63632187 TTCTATGTAGACTCTGCCACCATTGGTCATAGATCTGTTCTATAATTCATTTAATTTTTAGGGAA TTCTATGTAGACTCTGCCACCATTGGTCATAGGTCTGTTCTATAATTCATTTAATTTTTAGGGAA T C ATL3 Ensembl:ENSG00000184743 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170278182 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_354405,RMVar_hsa_circ_357792,RMVar_hsa_circ_274916,RMVar_hsa_circ_150354,RMVar_hsa_circ_150355 3438 RMVar_ID_3438 Human_SNP_ID_469535429 A-to-I Human chr11 - 63653771 63653771 63653771 TGTCTCCATAGTTTCGCCTTTACCAGAATGTCATATAGTTAGAATCATACAATATGCAGCCTTTT TGTCTCCATAGTTTCGCCTTTACCAGAATGTCGTATAGTTAGAATCATACAATATGCAGCCTTTT T C ATL3 Ensembl:ENSG00000184743 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs558768 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_359466,RMVar_hsa_circ_344857,RMVar_hsa_circ_150358,RMVar_hsa_circ_150359,RMVar_hsa_circ_343670 3439 RMVar_ID_3439 Human_SNP_ID_469537797 A-to-I Human chr11 - 63662653 63662652 63662653 GCAACATGGTGAAACACTGTCTCTCCAAAAATACAAAAATTAGCTGGGTGTGGTGATGAATGCCT GCAACATGGTGAAACACTGTCTCTCCAAAAAT_CAAAAATTAGCTGGGTGTGGTGATGAATGCCT GT G ATL3 Ensembl:ENSG00000184743 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1257488041 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_27641 3440 RMVar_ID_3440 Human_SNP_ID_469537817 A-to-I Human chr11 - 63662745 63662745 63662745 TCTTGGCTGGGTACGGTGTCGCTGTAATCCCAACACTTTGGGAGGTTGAGACGAGTGGATCATTT TCTTGGCTGGGTACGGTGTCGCTGTAATCCCAGCACTTTGGGAGGTTGAGACGAGTGGATCATTT T C ATL3 Ensembl:ENSG00000184743 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs980465007 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27641 3441 RMVar_ID_3441 Human_SNP_ID_469537818 A-to-I Human chr11 - 63662745 63662745 63662745 TCTTGGCTGGGTACGGTGTCGCTGTAATCCCAACACTTTGGGAGGTTGAGACGAGTGGATCATTT TCTTGGCTGGGTACGGTGTCGCTGTAATCCCACCACTTTGGGAGGTTGAGACGAGTGGATCATTT T G ATL3 Ensembl:ENSG00000184743 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs980465007 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27641 3442 RMVar_ID_3442 Human_SNP_ID_469537970 A-to-I Human chr11 - 63663355 63663355 63663355 GCATTCTGGGAGGCTGAGGTGAGAGGATCACTAGAGCCCAGGAGTTTGAGACTAATGTGGGCCAC GCATTCTGGGAGGCTGAGGTGAGAGGATCACTGGAGCCCAGGAGTTTGAGACTAATGTGGGCCAC T C ATL3 Ensembl:ENSG00000184743 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1048267076 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27641 3443 RMVar_ID_3443 Human_SNP_ID_469538600 A-to-I Human chr11 - 63665811 63665811 63665811 CCTGATTGTAGTGCAGTGGTTGACTTACTGCAACCTCTGCCTCCCAGGTTCAAGTGATACCAAGT CCTGATTGTAGTGCAGTGGTTGACTTACTGCAGCCTCTGCCTCCCAGGTTCAAGTGATACCAAGT T C ATL3 Ensembl:ENSG00000184743 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1018363832 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27641 3444 RMVar_ID_3444 Human_SNP_ID_469544635 A-to-I Human chr11 + 63686753 63686753 63686753 CACTTAGGAGACTGAGGTAGGAGGATGGCTTGAGCTGGGGGCAGAGGTTGCAGTGAGCTGAGATT CACTTAGGAGACTGAGGTAGGAGGATGGCTTGGGCTGGGGGCAGAGGTTGCAGTGAGCTGAGATT A G RTN3 Ensembl:ENSG00000133318 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1379016841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6083468,Human_RBP_ID_22491487 3445 RMVar_ID_3445 Human_SNP_ID_469546609 A-to-I Human chr11 + 63694585 63694585 63694585 ACGTCCATGTCCTGGGCTCAAGCCGTCCTCCCACCTCAGCCTCCGGAGTAGCTAGGACTGTAGGC ACGTCCATGTCCTGGGCTCAAGCCGTCCTCCCGCCTCAGCCTCCGGAGTAGCTAGGACTGTAGGC A G RTN3 Ensembl:ENSG00000133318 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1297322850 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11662385 3446 RMVar_ID_3446 Human_SNP_ID_469547324 A-to-I Human chr11 + 63697091 63697091 63697091 TATTTTTAGTAGAGATGGGGTTTCACCATGTTAGCCAAGGTGGTCTTGATCTCCTGACCTCGTGA TATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAAGGTGGTCTTGATCTCCTGACCTCGTGA A G RTN3 Ensembl:ENSG00000133318 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1230073245 Functional Loss SNV dbSNP153 33..33 33 - - - 3447 RMVar_ID_3447 Human_SNP_ID_469547765 A-to-I Human chr11 + 63698666 63698666 63698666 GGGAAACTTAACATGATCTAAGATCACTGAGGAACCATTGACTCCAGATACTGTCTTGTACATGA GGGAAACTTAACATGATCTAAGATCACTGAGGGACCATTGACTCCAGATACTGTCTTGTACATGA A G RTN3 Ensembl:ENSG00000133318 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1175581387 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11662444 3448 RMVar_ID_3448 Human_SNP_ID_469547773 A-to-I Human chr11 + 63698695 63698695 63698695 AGGAACCATTGACTCCAGATACTGTCTTGTACATGAGGCAAGGCTGGGAGAGGTTGTTCCGACTG AGGAACCATTGACTCCAGATACTGTCTTGTACGTGAGGCAAGGCTGGGAGAGGTTGTTCCGACTG A G RTN3 Ensembl:ENSG00000133318 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1220299452 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11662446 3449 RMVar_ID_3449 Human_SNP_ID_469547774 A-to-I Human chr11 + 63698702 63698702 63698702 ATTGACTCCAGATACTGTCTTGTACATGAGGCAAGGCTGGGAGAGGTTGTTCCGACTGACTGCCA ATTGACTCCAGATACTGTCTTGTACATGAGGCGAGGCTGGGAGAGGTTGTTCCGACTGACTGCCA A G RTN3 Ensembl:ENSG00000133318 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs540085949 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11662447 3450 RMVar_ID_3450 Human_SNP_ID_469550155 A-to-I Human chr11 + 63707592 63707592 63707592 GCGGTGGCTCACACCTGTAATCCTAGCACTTTAGGAGGCTGAGGCAGGCGGATCACCTGACGTCA GCGGTGGCTCACACCTGTAATCCTAGCACTTTCGGAGGCTGAGGCAGGCGGATCACCTGACGTCA A C RTN3 Ensembl:ENSG00000133318 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1268366587 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17991,RMVar_hsa_circ_297956,RMVar_hsa_circ_313966,RMVar_hsa_circ_150364 3451 RMVar_ID_3451 Human_SNP_ID_469550156 A-to-I Human chr11 + 63707592 63707592 63707592 GCGGTGGCTCACACCTGTAATCCTAGCACTTTAGGAGGCTGAGGCAGGCGGATCACCTGACGTCA GCGGTGGCTCACACCTGTAATCCTAGCACTTTGGGAGGCTGAGGCAGGCGGATCACCTGACGTCA A G RTN3 Ensembl:ENSG00000133318 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1268366587 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17991,RMVar_hsa_circ_297956,RMVar_hsa_circ_313966,RMVar_hsa_circ_150364 3452 RMVar_ID_3452 Human_SNP_ID_469550342 A-to-I Human chr11 + 63708359 63708359 63708359 GTAATAATAGGACTTAAAAAAAAAATAGAGACAAGGTCTCACTAGATTGCCCAGGCTGAACTCCT GTAATAATAGGACTTAAAAAAAAAATAGAGACGAGGTCTCACTAGATTGCCCAGGCTGAACTCCT A G RTN3 Ensembl:ENSG00000133318 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432047217 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17991,RMVar_hsa_circ_297956,RMVar_hsa_circ_313966,RMVar_hsa_circ_150364 3453 RMVar_ID_3453 Human_SNP_ID_469551041 A-to-I Human chr11 + 63711421 63711417 63711421 TTTTTTGTTATTTTTTTTTGAGACAGGGTCTCACTCTGTTGCCCAGGCTGGAGTGCAGTGGGTCA TTTTTTGTTATTTTTTTTTGAGACAGGGT____CTCTGTTGCCCAGGCTGGAGTGCAGTGGGTCA TCTCA T RTN3 Ensembl:ENSG00000133318 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs975031334 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_17991,RMVar_hsa_circ_297956,RMVar_hsa_circ_313966,RMVar_hsa_circ_150364 3454 RMVar_ID_3454 Human_SNP_ID_469551105 A-to-I Human chr11 + 63711682 63711682 63711682 TGCCTCCCAGGTTCAAGTGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGAATTACAGGCATGCA TGCCTCCCAGGTTCAAGTGATTCTCCTGCCTCGGCCTCCTGAGTAGCTGGAATTACAGGCATGCA A G RTN3 Ensembl:ENSG00000133318 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs771814882 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17991,RMVar_hsa_circ_297956,RMVar_hsa_circ_313966,RMVar_hsa_circ_150364 3455 RMVar_ID_3455 Human_SNP_ID_469551407 A-to-I Human chr11 + 63712834 63712834 63712834 TAAGAATTTTTTGGCCGGGCGCAATGGCTCACACTTGTAATCCCAGCACTTGGAGAGGCCGAGGC TAAGAATTTTTTGGCCGGGCGCAATGGCTCACGCTTGTAATCCCAGCACTTGGAGAGGCCGAGGC A G RTN3 Ensembl:ENSG00000133318 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025926488 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227623,Human_RBP_ID_11760032,Human_RBP_ID_17560347 RMVar_hsa_circ_17991,RMVar_hsa_circ_297956,RMVar_hsa_circ_313966,RMVar_hsa_circ_150364 3456 RMVar_ID_3456 Human_SNP_ID_469551891 A-to-I Human chr11 + 63714710 63714710 63714710 AATTTTTCTATTTTTTGTAGGGGCAGGATCTCAGCATGTTGCCCAGGCTGATCTTGACCTCTTGG AATTTTTCTATTTTTTGTAGGGGCAGGATCTCGGCATGTTGCCCAGGCTGATCTTGACCTCTTGG A G RTN3 Ensembl:ENSG00000133318 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,cerebellum - 29129909,30559470 RNA-Seq:(High) rs888833153 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17991,RMVar_hsa_circ_297956,RMVar_hsa_circ_313966,RMVar_hsa_circ_150364 3457 RMVar_ID_3457 Human_SNP_ID_469551892 A-to-I Human chr11 + 63714713 63714713 63714713 TTTTCTATTTTTTGTAGGGGCAGGATCTCAGCATGTTGCCCAGGCTGATCTTGACCTCTTGGACT TTTTCTATTTTTTGTAGGGGCAGGATCTCAGCCTGTTGCCCAGGCTGATCTTGACCTCTTGGACT A C RTN3 Ensembl:ENSG00000133318 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1381307896 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17991,RMVar_hsa_circ_297956,RMVar_hsa_circ_313966,RMVar_hsa_circ_150364 3458 RMVar_ID_3458 Human_SNP_ID_469556120 A-to-I Human chr11 + 63729583 63729583 63729583 GGGCTCAAGCAATCCTCGTGCCTCAGCCTCCCATGTACCTGGGACCACAGGTGCATGCCACCACA GGGCTCAAGCAATCCTCGTGCCTCAGCCTCCCGTGTACCTGGGACCACAGGTGCATGCCACCACA A G RTN3 Ensembl:ENSG00000133318 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1368972480 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17991,RMVar_hsa_circ_313966,RMVar_hsa_circ_286693,RMVar_hsa_circ_336977 3459 RMVar_ID_3459 Human_SNP_ID_469556948 A-to-I Human chr11 + 63733057 63733057 63733057 ATAATCAGGGCTGGGCTCAGTGGCTCACGCCTATAATCCTAGCACTTTGGGAGGCCGAGGCAGGT ATAATCAGGGCTGGGCTCAGTGGCTCACGCCTGTAATCCTAGCACTTTGGGAGGCCGAGGCAGGT A G RTN3 Ensembl:ENSG00000133318 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1229618788 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17991,RMVar_hsa_circ_313966,RMVar_hsa_circ_286693,RMVar_hsa_circ_336977 3460 RMVar_ID_3460 Human_SNP_ID_469557644 A-to-I Human chr11 + 63735179 63735179 63735179 ACTTGGCTAATTTTTGTAATTGTAGTAGAGACAGGGTTTCATCTTGTTGCCCAGGCTGGTCTCGA ACTTGGCTAATTTTTGTAATTGTAGTAGAGACCGGGTTTCATCTTGTTGCCCAGGCTGGTCTCGA A C RTN3 Ensembl:ENSG00000133318 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs373792971 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17991,RMVar_hsa_circ_313966,RMVar_hsa_circ_286693,RMVar_hsa_circ_336977 3461 RMVar_ID_3461 Human_SNP_ID_469558268 A-to-I Human chr11 + 63737086 63737086 63737086 TGCCTCCTGGGCTCAAGGGATCCTCCCACCTCAGCCTCCTGAGTAGCTGGGACTACGGGTATACG TGCCTCCTGGGCTCAAGGGATCCTCCCACCTCGGCCTCCTGAGTAGCTGGGACTACGGGTATACG A G RTN3 Ensembl:ENSG00000133318 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1405135382 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17991,RMVar_hsa_circ_313966,RMVar_hsa_circ_286693,RMVar_hsa_circ_336977 3462 RMVar_ID_3462 Human_SNP_ID_469561139 A-to-I Human chr11 + 63748610 63748610 63748610 GGCCTCAAGTGATCCACCAGCCTCGGACTCCCAAAGTGCAGAGATTACAGGCGTGAGCCCCTGCA GGCCTCAAGTGATCCACCAGCCTCGGACTCCCGAAGTGCAGAGATTACAGGCGTGAGCCCCTGCA A G RTN3 Ensembl:ENSG00000133318 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1032918620 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17991,RMVar_hsa_circ_313966,RMVar_hsa_circ_321910,RMVar_hsa_circ_286693,RMVar_hsa_circ_336977 3463 RMVar_ID_3463 Human_SNP_ID_469561680 A-to-I Human chr11 + 63750635 63750635 63750635 CCACTATGCCCAGCTAATTTTGTATTTTTACTAGATACGGGGTTTCTCTATGTTGGTCAGGCTGG CCACTATGCCCAGCTAATTTTGTATTTTTACTCGATACGGGGTTTCTCTATGTTGGTCAGGCTGG A C RTN3 Ensembl:ENSG00000133318 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1458706890 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11663098 RMVar_hsa_circ_17991,RMVar_hsa_circ_315466,RMVar_hsa_circ_270844 3464 RMVar_ID_3464 Human_SNP_ID_469561681 A-to-I Human chr11 + 63750635 63750635 63750635 CCACTATGCCCAGCTAATTTTGTATTTTTACTAGATACGGGGTTTCTCTATGTTGGTCAGGCTGG CCACTATGCCCAGCTAATTTTGTATTTTTACTGGATACGGGGTTTCTCTATGTTGGTCAGGCTGG A G RTN3 Ensembl:ENSG00000133318 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1458706890 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11663098 RMVar_hsa_circ_17991,RMVar_hsa_circ_315466,RMVar_hsa_circ_270844 3465 RMVar_ID_3465 Human_SNP_ID_469580373 A-to-I Human chr11 + 63819288 63819288 63819288 GCTGGCATGTAGTAGCACAAGCCCGGCTCACTACAACCTCTGCCTCCCAGGTTCAAGCAATTCTC GCTGGCATGTAGTAGCACAAGCCCGGCTCACTGCAACCTCTGCCTCCCAGGTTCAAGCAATTCTC A G SPINDOC Ensembl:ENSG00000168005 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1482118820 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24894060 RMVar_hsa_circ_78377,RMVar_hsa_circ_150371,RMVar_hsa_circ_97315,RMVar_hsa_circ_150372,RMVar_hsa_circ_150378,RMVar_hsa_circ_101809 3466 RMVar_ID_3466 Human_SNP_ID_469580406 A-to-I Human chr11 + 63819368 63819368 63819368 TAGTAGCTGGGATTACAGGCGTGCGCCACCATACCCGGCTAATTTTTGTATTTTTAGTAGAGACA TAGTAGCTGGGATTACAGGCGTGCGCCACCATGCCCGGCTAATTTTTGTATTTTTAGTAGAGACA A G SPINDOC Ensembl:ENSG00000168005 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1235127145 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 3467 RMVar_ID_3467 Human_SNP_ID_469580960 A-to-I Human chr11 + 63821001 63821001 63821001 TTCAGCCCAGGAGTTCAAGGCTGCAATGAGCTATGATCACACCACTGCACTCCAGCCTGGACGAC TTCAGCCCAGGAGTTCAAGGCTGCAATGAGCTGTGATCACACCACTGCACTCCAGCCTGGACGAC A G SPINDOC Ensembl:ENSG00000168005 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs941092985 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23305126 RMVar_hsa_circ_78377,RMVar_hsa_circ_150371,RMVar_hsa_circ_97315,RMVar_hsa_circ_150372,RMVar_hsa_circ_150378,RMVar_hsa_circ_101809 3468 RMVar_ID_3468 Human_SNP_ID_469581155 A-to-I Human chr11 + 63821983 63821983 63821983 GTTGCCCAAGCTAGTCTCCAACTCCTGGGTGCAAGCAGTCCTCCCACCTGGGCCTCCCAAAGTTC GTTGCCCAAGCTAGTCTCCAACTCCTGGGTGCTAGCAGTCCTCCCACCTGGGCCTCCCAAAGTTC A T SPINDOC Ensembl:ENSG00000168005 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs111526878 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17559999 RMVar_hsa_circ_78377,RMVar_hsa_circ_150371,RMVar_hsa_circ_97315,RMVar_hsa_circ_150372,RMVar_hsa_circ_150378,RMVar_hsa_circ_101809 3469 RMVar_ID_3469 Human_SNP_ID_469581195 A-to-I Human chr11 + 63822172 63822172 63822172 CGAGACCAACCTGAGCAACATAAGGAGACTCCATCTCTAGAAAAATTTTTTAAATTAACTGGGCA CGAGACCAACCTGAGCAACATAAGGAGACTCCGTCTCTAGAAAAATTTTTTAAATTAACTGGGCA A G SPINDOC Ensembl:ENSG00000168005 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264001962 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 3470 RMVar_ID_3470 Human_SNP_ID_469581202 A-to-I Human chr11 + 63822196 63822196 63822196 GAGACTCCATCTCTAGAAAAATTTTTTAAATTAACTGGGCATGTTGGTGTGCACCTCTAGTCCCT GAGACTCCATCTCTAGAAAAATTTTTTAAATTGACTGGGCATGTTGGTGTGCACCTCTAGTCCCT A G SPINDOC Ensembl:ENSG00000168005 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1055931 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11663510,Human_RBP_ID_17560640 RMVar_hsa_circ_78377,RMVar_hsa_circ_150371,RMVar_hsa_circ_97315,RMVar_hsa_circ_150372,RMVar_hsa_circ_150378,RMVar_hsa_circ_101809 3471 RMVar_ID_3471 Human_SNP_ID_469581215 A-to-I Human chr11 + 63822245 63822245 63822245 TGCACCTCTAGTCCCTACTAAGACTAGAGGCTAAGGCAAGAGGATCACTTGAGCCCAAGAATTTG TGCACCTCTAGTCCCTACTAAGACTAGAGGCTGAGGCAAGAGGATCACTTGAGCCCAAGAATTTG A G SPINDOC Ensembl:ENSG00000168005 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1304227373 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11663512 RMVar_hsa_circ_78377,RMVar_hsa_circ_150371,RMVar_hsa_circ_97315,RMVar_hsa_circ_150372,RMVar_hsa_circ_150378,RMVar_hsa_circ_101809 3472 RMVar_ID_3472 Human_SNP_ID_469581220 A-to-I Human chr11 + 63822259 63822259 63822259 CTACTAAGACTAGAGGCTAAGGCAAGAGGATCACTTGAGCCCAAGAATTTGAGGTTGCAGTAAAT CTACTAAGACTAGAGGCTAAGGCAAGAGGATCGCTTGAGCCCAAGAATTTGAGGTTGCAGTAAAT A G SPINDOC Ensembl:ENSG00000168005 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1134210 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 3473 RMVar_ID_3473 Human_SNP_ID_469584966 A-to-I Human chr11 - 63836885 63836885 63836885 TCTGCTGTCACCATCTTGAAATTTTTTTTTTTAAGACTGAATCTCGCTCTATCTCCCAGGCTGGA TCTGCTGTCACCATCTTGAAATTTTTTTTTTTTAGACTGAATCTCGCTCTATCTCCCAGGCTGGA T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1408869558 Functional Loss SNV dbSNP153 33..33 33 - - - 3474 RMVar_ID_3474 Human_SNP_ID_469588562 A-to-I Human chr11 + 63851352 63851352 63851352 ATGGAGATGCCAGGCATAGTGGAGGCTGAGGCAGGAGGGTCACTTGAGGCTGGAGGATTGCTTGA ATGGAGATGCCAGGCATAGTGGAGGCTGAGGCTGGAGGGTCACTTGAGGCTGGAGGATTGCTTGA A T MARK2 Ensembl:ENSG00000072518 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs923595296 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6083793,Human_RBP_ID_11663950 3475 RMVar_ID_3475 Human_SNP_ID_469589222 A-to-I Human chr11 + 63854107 63854107 63854107 GTTGGCCGGGCTGGTCTGGAATTCCTGACCTCAGGTGATCCACCTGCCTCGGCCTCCCAAAGTGC GTTGGCCGGGCTGGTCTGGAATTCCTGACCTCCGGTGATCCACCTGCCTCGGCCTCCCAAAGTGC A C MARK2 Ensembl:ENSG00000072518 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1196430278 Functional Loss SNV dbSNP153 33..33 33 - - - 3476 RMVar_ID_3476 Human_SNP_ID_469592320 A-to-I Human chr11 + 63864755 63864755 63864755 AGGGCTGGATGTAGTCGGTGGCTCACAGCTGTATTCTCAGCACTTTGGGAGGCCAAGGTGAGAGG AGGGCTGGATGTAGTCGGTGGCTCACAGCTGTTTTCTCAGCACTTTGGGAGGCCAAGGTGAGAGG A T MARK2 Ensembl:ENSG00000072518 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1010526708 Functional Loss SNV dbSNP153 33..33 33 - - - 3477 RMVar_ID_3477 Human_SNP_ID_469614553 A-to-I Human chr11 + 63947286 63947286 63947286 AAAAATTAGCTGGCACGGTGGCGATCGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAAATTAGCTGGCACGGTGGCGATCGCCTGTTATCCCAGCTACTCGGGAGGCTGAGGCAGGAGA A T NAA40 Ensembl:ENSG00000110583 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs549989881 Functional Loss SNV dbSNP153 33..33 33 - - - 3478 RMVar_ID_3478 Human_SNP_ID_469614780 A-to-I Human chr11 + 63948129 63948129 63948129 CACCTGCCTCAGCCACCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCGCCTGGCCTGATGTC CACCTGCCTCAGCCACCCAAAGTGCTGGGATTGCAGGTGTGAGCCACCGCGCCTGGCCTGATGTC A G NAA40 Ensembl:ENSG00000110583 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1395872817 Functional Loss SNV dbSNP153 33..33 33 - - - 3479 RMVar_ID_3479 Human_SNP_ID_469617190 A-to-I Human chr11 + 63956879 63956879 63956879 CCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGACTCGCTTGAACCCAGGAGGTGGAGGTT CCTGTAATCCCAGCTACTCGGGAGGCTGAGGCGGGAGACTCGCTTGAACCCAGGAGGTGGAGGTT A G NAA40 Ensembl:ENSG00000110583 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1402498532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_399642 3480 RMVar_ID_3480 Human_SNP_ID_469618294 A-to-I Human chr11 + 63960470 63960470 63960470 GAGACAAGATCTCTGTCACCAGGCTGGAGTGCAGTGGCACAATCAGCTCACTGCAGCCTCAACCT GAGACAAGATCTCTGTCACCAGGCTGGAGTGCGGTGGCACAATCAGCTCACTGCAGCCTCAACCT A G RF00017-2364 RNACentral:URS000096BB03 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1310648623 Functional Loss SNV dbSNP153 33..33 33 - - - 3481 RMVar_ID_3481 Human_SNP_ID_469619127 A-to-I Human chr11 + 63963655 63963655 63963655 GATTAGGAGTTCGAGACCAGCCTGGGCAACATAGCGAGACCTCATCTCTACTAAAAATAAAAAAT GATTAGGAGTTCGAGACCAGCCTGGGCAACATTGCGAGACCTCATCTCTACTAAAAATAAAAAAT A T RF00017-2364 RNACentral:URS000096BB03 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1045149626 Functional Loss SNV dbSNP153 33..33 33 - - - 3482 RMVar_ID_3482 Human_SNP_ID_469619970 A-to-I Human chr11 + 63966444 63966444 63966444 TTTTGTATTTTTAGTGGAGATGGGGTTTCACCATGTTGGCTAGGCTGGTCTTGAACTCCTGACTT TTTTGTATTTTTAGTGGAGATGGGGTTTCACCGTGTTGGCTAGGCTGGTCTTGAACTCCTGACTT A G RF00017-2364 RNACentral:URS000096BB03 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1032976658 Functional Loss SNV dbSNP153 33..33 33 - - - 3483 RMVar_ID_3483 Human_SNP_ID_469620746 A-to-I Human chr11 + 63969137 63969137 63969137 TGGACTTCGTGATTTGCCCATCTCGGCCTCCCAAAGTGCTGGGGTTACAGGCGTAAGCCAAGCCT TGGACTTCGTGATTTGCCCATCTCGGCCTCCCGAAGTGCTGGGGTTACAGGCGTAAGCCAAGCCT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs540036452 Functional Loss SNV dbSNP153 33..33 33 - - - 3484 RMVar_ID_3484 Human_SNP_ID_469620747 A-to-I Human chr11 + 63969137 63969137 63969137 TGGACTTCGTGATTTGCCCATCTCGGCCTCCCAAAGTGCTGGGGTTACAGGCGTAAGCCAAGCCT TGGACTTCGTGATTTGCCCATCTCGGCCTCCCTAAGTGCTGGGGTTACAGGCGTAAGCCAAGCCT A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs540036452 Functional Loss SNV dbSNP153 33..33 33 - - - 3485 RMVar_ID_3485 Human_SNP_ID_469620748 A-to-I Human chr11 + 63969138 63969138 63969138 GGACTTCGTGATTTGCCCATCTCGGCCTCCCAAAGTGCTGGGGTTACAGGCGTAAGCCAAGCCTG GGACTTCGTGATTTGCCCATCTCGGCCTCCCAGAGTGCTGGGGTTACAGGCGTAAGCCAAGCCTG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1311968107 Functional Loss SNV dbSNP153 33..33 33 - - - 3486 RMVar_ID_3486 Human_SNP_ID_469620751 A-to-I Human chr11 + 63969153 63969153 63969153 CCCATCTCGGCCTCCCAAAGTGCTGGGGTTACAGGCGTAAGCCAAGCCTGGCCCAGACAACTTTG CCCATCTCGGCCTCCCAAAGTGCTGGGGTTACCGGCGTAAGCCAAGCCTGGCCCAGACAACTTTG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1366684693 Functional Loss SNV dbSNP153 33..33 33 - - - 3487 RMVar_ID_3487 Human_SNP_ID_469624613 A-to-I Human chr11 + 63983454 63983453 63983455 CGCCACCGTGCCTGACTAATTTTTGTGTTTTTAGTAGAGACGGGGTTTCACCATCTTGACCAGGC CGCCACCGTGCCTGACTAATTTTTGTGTTTTT__TAGAGACGGGGTTTCACCATCTTGACCAGGC TAG T AP000721.1 Ensembl:ENSG00000256100 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1472085018 Functional Loss DEL dbSNP153 33..34 33 - - - 3488 RMVar_ID_3488 Human_SNP_ID_469666518 A-to-I Human chr11 - 64143067 64143067 64143067 CACTGTTCCCCAGGCTGGAGTACAGTGGTGCAATCATGGCTCACTGCAGCCTCCACCTCCTGGGG CACTGTTCCCCAGGCTGGAGTACAGTGGTGCAGTCATGGCTCACTGCAGCCTCCACCTCCTGGGG T C MACROD1 Ensembl:ENSG00000133315 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs993458626 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19697076 RMVar_hsa_circ_78649,RMVar_hsa_circ_98980,RMVar_hsa_circ_150396,RMVar_hsa_circ_79831,RMVar_hsa_circ_150397,RMVar_hsa_circ_150398 3489 RMVar_ID_3489 Human_SNP_ID_469667654 A-to-I Human chr11 - 64147203 64147203 64147203 AAGATTAGTAGGGTGTGGTGGTGCATGCCTGTAGTCCAGCTACTTGGGAGGCTGAAGTGGGAGGA AAGATTAGTAGGGTGTGGTGGTGCATGCCTGTTGTCCAGCTACTTGGGAGGCTGAAGTGGGAGGA T A MACROD1 Ensembl:ENSG00000133315 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1325677922 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5235042 RMVar_hsa_circ_78649,RMVar_hsa_circ_98980,RMVar_hsa_circ_150396,RMVar_hsa_circ_79831,RMVar_hsa_circ_150397,RMVar_hsa_circ_150398 3490 RMVar_ID_3490 Human_SNP_ID_469675321 A-to-I Human chr11 - 64175547 64175547 64175547 TTAGACGGAGTTTAGCTATCTTTGCCCAGGCTAGAGTGCAATAGCGTGATCTTGGCTCACCACAA TTAGACGGAGTTTAGCTATCTTTGCCCAGGCTGGAGTGCAATAGCGTGATCTTGGCTCACCACAA T C lnc-MACROD1-1,lnc-MACROD1-1:2,lnc-MACROD1-1:3,lnc-MACROD1-1:4 RNACentral:URS0000D5E196,RNACentral:URS00008BBAD0,RNACentral:URS0000D5927D,RNACentral:URS0000D57BCC lincRNA,lincRNA,lincRNA,lincRNA exon,intron,exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs925053575 Functional Loss SNV dbSNP153 33..33 33 - - - 3491 RMVar_ID_3491 Human_SNP_ID_469676027 A-to-I Human chr11 - 64178018 64178018 64178018 AAAATTAGCTGGATGTGGTGACACACGCCTGTAGCCCCAGCTGCTCAGGAGGCTGAGGCAGGAGA AAAATTAGCTGGATGTGGTGACACACGCCTGTTGCCCCAGCTGCTCAGGAGGCTGAGGCAGGAGA T A lnc-MACROD1-1,lnc-MACROD1-1:2,lnc-MACROD1-1:3,lnc-MACROD1-1:4,lnc-MACROD1-1:5 RNACentral:URS0000D5E196,RNACentral:URS00008C0BD2,RNACentral:URS0000D5927D,RNACentral:URS0000D57BCC,RNACentral:URS0000D57694 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1565273180 Functional Loss SNV dbSNP153 33..33 33 - - - 3492 RMVar_ID_3492 Human_SNP_ID_469679178 A-to-I Human chr11 + 64187894 64187894 64187894 GGGCGTGGTGGCGGGAGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGACGTGAA GGGCGTGGTGGCGGGAGCCTGTAGTCCCAGCTGCTCGGGAGGCTGAGGCAGGAGAATGACGTGAA A G STIP1 Ensembl:ENSG00000168439 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1321392336 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109104,RMVar_hsa_circ_150402 3493 RMVar_ID_3493 Human_SNP_ID_469679280 A-to-I Human chr11 + 64188137 64188137 64188137 GGGAGGCCAAGGTGGGCGAATCACCTGAGGTCAGGAGTTCTACACCAGCCTGGCCAACATGGTGA GGGAGGCCAAGGTGGGCGAATCACCTGAGGTCGGGAGTTCTACACCAGCCTGGCCAACATGGTGA A G STIP1 Ensembl:ENSG00000168439 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1485092743 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109104,RMVar_hsa_circ_150402 3494 RMVar_ID_3494 Human_SNP_ID_469679401 A-to-I Human chr11 + 64188411 64188410 64188412 TACCAAATTTATTTTGTATTTTTTTTAGAGACAGGGTCTGGTTCTGTGGCCCAGGCTGAAGTGCC TACCAAATTTATTTTGTATTTTTTTTAGAGAC__GGTCTGGTTCTGTGGCCCAGGCTGAAGTGCC CAG C STIP1 Ensembl:ENSG00000168439 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1321528411 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_109104,RMVar_hsa_circ_150402 3495 RMVar_ID_3495 Human_SNP_ID_469679402 A-to-I Human chr11 + 64188411 64188411 64188411 TACCAAATTTATTTTGTATTTTTTTTAGAGACAGGGTCTGGTTCTGTGGCCCAGGCTGAAGTGCC TACCAAATTTATTTTGTATTTTTTTTAGAGACCGGGTCTGGTTCTGTGGCCCAGGCTGAAGTGCC A C STIP1 Ensembl:ENSG00000168439 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1276818908 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109104,RMVar_hsa_circ_150402 3496 RMVar_ID_3496 Human_SNP_ID_469679465 A-to-I Human chr11 + 64188651 64188651 64188651 CTCTAGCCTTGGCCTCCCACTTCATTAGCACTAGGATTACAGGCGTGAGTCACCTTGCCTGGTCT CTCTAGCCTTGGCCTCCCACTTCATTAGCACTGGGATTACAGGCGTGAGTCACCTTGCCTGGTCT A G STIP1 Ensembl:ENSG00000168439 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1162648312 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11666577 RMVar_hsa_circ_109104,RMVar_hsa_circ_150402 3497 RMVar_ID_3497 Human_SNP_ID_469679706 A-to-I Human chr11 + 64189416 64189416 64189416 GGACATTGTGGTGCGCGCCTGTGGTCCCAGCTACGTGGGAGGCTGAGGCAGGACAATTGCTTGAA GGACATTGTGGTGCGCGCCTGTGGTCCCAGCTGCGTGGGAGGCTGAGGCAGGACAATTGCTTGAA A G STIP1 Ensembl:ENSG00000168439 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1040187825 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109104,RMVar_hsa_circ_150402 3498 RMVar_ID_3498 Human_SNP_ID_469679969 A-to-I Human chr11 + 64190171 64190171 64190171 TACAGGCATGCACCACCACATCCGGGCAATTTATTTATTTATTTATTTTTTTGAGACTGAGTTTC TACAGGCATGCACCACCACATCCGGGCAATTTTTTTATTTATTTATTTTTTTGAGACTGAGTTTC A T STIP1 Ensembl:ENSG00000168439 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1444146740 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109104,RMVar_hsa_circ_150402 3499 RMVar_ID_3499 Human_SNP_ID_469682692 A-to-I Human chr11 + 64198944 64198944 64198944 AGCAATAGCCGGGTGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGTGG AGCAATAGCCGGGTGCAGTGGCTCACGCCTGTGATCCCAGCACTTTGGGAGGCTGAGGTGGGTGG A G STIP1 Ensembl:ENSG00000168439 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1333423724 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109104,RMVar_hsa_circ_92848,RMVar_hsa_circ_150402,RMVar_hsa_circ_357732,RMVar_hsa_circ_303371,RMVar_hsa_circ_55185,RMVar_hsa_circ_128188,RMVar_hsa_circ_150406,RMVar_hsa_circ_150407,RMVar_hsa_circ_96407,RMVar_hsa_circ_357624,RMVar_hsa_circ_59829,RMVar_hsa_circ_115382,RMVar_hsa_circ_150409,RMVar_hsa_circ_150411,RMVar_hsa_circ_86974,RMVar_hsa_circ_88483,RMVar_hsa_circ_23312,RMVar_hsa_circ_124256,RMVar_hsa_circ_150412,RMVar_hsa_circ_150414,RMVar_hsa_circ_97306,RMVar_hsa_circ_150415,RMVar_hsa_circ_150416,RMVar_hsa_circ_94190,RMVar_hsa_circ_150418,RMVar_hsa_circ_150419 3500 RMVar_ID_3500 Human_SNP_ID_469682968 A-to-I Human chr11 + 64199703 64199703 64199703 CTCCTGCCTCAGTCTCCCGAGTAGCTGGGACTACAGGCTCCCGCCACCACACCAGGCTAATTTTT CTCCTGCCTCAGTCTCCCGAGTAGCTGGGACTGCAGGCTCCCGCCACCACACCAGGCTAATTTTT A G STIP1 Ensembl:ENSG00000168439 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs960074036 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109104,RMVar_hsa_circ_92848,RMVar_hsa_circ_150402,RMVar_hsa_circ_357732,RMVar_hsa_circ_303371,RMVar_hsa_circ_55185,RMVar_hsa_circ_128188,RMVar_hsa_circ_150406,RMVar_hsa_circ_150407,RMVar_hsa_circ_96407,RMVar_hsa_circ_357624,RMVar_hsa_circ_59829,RMVar_hsa_circ_115382,RMVar_hsa_circ_150409,RMVar_hsa_circ_150411,RMVar_hsa_circ_86974,RMVar_hsa_circ_88483,RMVar_hsa_circ_23312,RMVar_hsa_circ_124256,RMVar_hsa_circ_150412,RMVar_hsa_circ_150414,RMVar_hsa_circ_97306,RMVar_hsa_circ_150415,RMVar_hsa_circ_150416,RMVar_hsa_circ_94190,RMVar_hsa_circ_150418,RMVar_hsa_circ_150419 3501 RMVar_ID_3501 Human_SNP_ID_469687826 A-to-I Human chr11 + 64215622 64215622 64215622 TAGAGATGGGGTCTCGCTCTGTCACCCAGACTAGAGTGCAGTGGTGCGATCATAGCTCACTGCAA TAGAGATGGGGTCTCGCTCTGTCACCCAGACTGGAGTGCAGTGGTGCGATCATAGCTCACTGCAA A G FERMT3 Ensembl:ENSG00000149781 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs772682968 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73548,RMVar_hsa_circ_85185,RMVar_hsa_circ_127561,RMVar_hsa_circ_150429,RMVar_hsa_circ_150430 3502 RMVar_ID_3502 Human_SNP_ID_469688604 A-to-I Human chr11 + 64218514 64218513 64218514 TTTAGTAGAGATAGGGTTTCACCATGTTGCCCAAGCTGGTCTGAAACTCCTGGGCTCAAGCTATC TTTAGTAGAGATAGGGTTTCACCATGTTGCCC_AGCTGGTCTGAAACTCCTGGGCTCAAGCTATC CA C FERMT3 Ensembl:ENSG00000149781 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1243304568 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_73548,RMVar_hsa_circ_85185,RMVar_hsa_circ_127561,RMVar_hsa_circ_150429,RMVar_hsa_circ_150430 3503 RMVar_ID_3503 Human_SNP_ID_469692106 A-to-I Human chr11 + 64228447 64228447 64228447 AGCACTTTGGGAGGCTGAGGTGGGCAGATCACAAGGTCAGGAGATCAAGACCATCCTGGCTAACA AGCACTTTGGGAGGCTGAGGTGGGCAGATCACGAGGTCAGGAGATCAAGACCATCCTGGCTAACA A G NUDT22 Ensembl:ENSG00000149761 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs901065069 Functional Loss SNV dbSNP153 33..33 33 - - - 3504 RMVar_ID_3504 Human_SNP_ID_469707584 A-to-I Human chr11 - 64273224 64273224 64273224 GGACTACAGGCGTGAACCACCACACCTAACTAATTTTTGTATTTTTAGTAGAGACGGAGTTTCAC GGACTACAGGCGTGAACCACCACACCTAACTAGTTTTTGTATTTTTAGTAGAGACGGAGTTTCAC T C BAD Ensembl:ENSG00000002330 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1357205626 Functional Loss SNV dbSNP153 33..33 33 - - - 3505 RMVar_ID_3505 Human_SNP_ID_469709795 A-to-I Human chr11 + 64281173 64281173 64281173 GTATTTTTAGTGGAGACGGGGTTCACCGTGTTAGCCAGAATGGTCTCTATCTCCTGACCTCATGA GTATTTTTAGTGGAGACGGGGTTCACCGTGTTGGCCAGAATGGTCTCTATCTCCTGACCTCATGA A G GPR137 Ensembl:ENSG00000173264 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1337096868 Functional Loss SNV dbSNP153 33..33 33 - - - 3506 RMVar_ID_3506 Human_SNP_ID_469709803 A-to-I Human chr11 + 64281213 64281213 64281213 TGGTCTCTATCTCCTGACCTCATGATCTGCCCACCTCGAACTACCAAAGTGCTGGGATTATAGGC TGGTCTCTATCTCCTGACCTCATGATCTGCCCGCCTCGAACTACCAAAGTGCTGGGATTATAGGC A G GPR137 Ensembl:ENSG00000173264 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1375875692 Functional Loss SNV dbSNP153 33..33 33 - - - 3507 RMVar_ID_3507 Human_SNP_ID_469717625 A-to-I Human chr11 + 64307916 64307915 64307917 AAGGCAGATTTTAATTTTTTTTTTTTTGAGACAGAGTCTCACTCTGTTGTTCAGGCTAGAGTGCA AAGGCAGATTTTAATTTTTTTTTTTTTGAGAC__AGTCTCACTCTGTTGTTCAGGCTAGAGTGCA CAG C ESRRA Ensembl:ENSG00000173153 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1165324381 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_22471631 3508 RMVar_ID_3508 Human_SNP_ID_469717630 A-to-I Human chr11 + 64307941 64307941 64307941 TTGAGACAGAGTCTCACTCTGTTGTTCAGGCTAGAGTGCAGTGGCACAATCTCTGCTCACTGCAA TTGAGACAGAGTCTCACTCTGTTGTTCAGGCTTGAGTGCAGTGGCACAATCTCTGCTCACTGCAA A T ESRRA Ensembl:ENSG00000173153 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1473030370 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17560647,Human_RBP_ID_22471631 3509 RMVar_ID_3509 Human_SNP_ID_469717928 A-to-I Human chr11 + 64308968 64308968 64308968 GAAACCCCGTCTCTACTGAAAATACAAAAATTAGCCAAGCATGGTGGCATGCGCCTGTCATCCCA GAAACCCCGTCTCTACTGAAAATACAAAAATTCGCCAAGCATGGTGGCATGCGCCTGTCATCCCA A C ESRRA Ensembl:ENSG00000173153 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs545656166 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17560358,Human_RBP_ID_22471632 3510 RMVar_ID_3510 Human_SNP_ID_469718137 A-to-I Human chr11 + 64309817 64309817 64309817 AGCCAGGTGTCGTGGTGGGTGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATTGCT AGCCAGGTGTCGTGGTGGGTGCCTGTAGTCCCGGCTACTCAGGAGGCTGAGGCAGGAGAATTGCT A G ESRRA Ensembl:ENSG00000173153 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1188493696 Functional Loss SNV dbSNP153 33..33 33 - - - 3511 RMVar_ID_3511 Human_SNP_ID_469718437 A-to-I Human chr11 + 64310908 64310908 64310908 TCCACCAATCTTAAACTTTGTGCACCCTTCCCACTCTGAAGAACAGTGAGCCAGCCGGCCAGGGT TCCACCAATCTTAAACTTTGTGCACCCTTCCCGCTCTGAAGAACAGTGAGCCAGCCGGCCAGGGT A G ESRRA Ensembl:ENSG00000173153 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs493052 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_97 3512 RMVar_ID_3512 Human_SNP_ID_469718958 A-to-I Human chr11 + 64312952 64312952 64312952 GGCAAGAAGCAGGGGCGTAGGCCTAGGAGGACATAGGTTCGCTTTGGCTTGGACTCAGAGAAGGG GGCAAGAAGCAGGGGCGTAGGCCTAGGAGGACGTAGGTTCGCTTTGGCTTGGACTCAGAGAAGGG A G ESRRA Ensembl:ENSG00000173153 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs620645 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26776370 3513 RMVar_ID_3513 Human_SNP_ID_469718959 A-to-I Human chr11 + 64312952 64312952 64312952 GGCAAGAAGCAGGGGCGTAGGCCTAGGAGGACATAGGTTCGCTTTGGCTTGGACTCAGAGAAGGG GGCAAGAAGCAGGGGCGTAGGCCTAGGAGGACTTAGGTTCGCTTTGGCTTGGACTCAGAGAAGGG A T ESRRA Ensembl:ENSG00000173153 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs620645 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26776370 3514 RMVar_ID_3514 Human_SNP_ID_469732415 A-to-I Human chr11 + 64356179 64356179 64356179 GCTAATTTTGTATAATTATTATTATTTTTTTTAGTAGAGACGGGGTTTCACCATGTTGGTCAGGC GCTAATTTTGTATAATTATTATTATTTTTTTTGGTAGAGACGGGGTTTCACCATGTTGGTCAGGC A G CCDC88B Ensembl:ENSG00000168071 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1390431838 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_111701 3515 RMVar_ID_3515 Human_SNP_ID_469732470 A-to-I Human chr11 + 64356434 64356434 64356434 GTCTCTACTAAAACTACAAAAATTAGCCAGGCATGGTGTCCCATGCCTGTAATCCCACCTACTCA GTCTCTACTAAAACTACAAAAATTAGCCAGGCGTGGTGTCCCATGCCTGTAATCCCACCTACTCA A G CCDC88B Ensembl:ENSG00000168071 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs188234219 Functional Loss SNV dbSNP153 33..33 33 - - - 3516 RMVar_ID_3516 Human_SNP_ID_469732479 A-to-I Human chr11 + 64356462 64356462 64356462 AGGCATGGTGTCCCATGCCTGTAATCCCACCTACTCAGGGGGCTGAGGCAGGAGAATCGCTTGAA AGGCATGGTGTCCCATGCCTGTAATCCCACCTCCTCAGGGGGCTGAGGCAGGAGAATCGCTTGAA A C CCDC88B Ensembl:ENSG00000168071 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1270074427 Functional Loss SNV dbSNP153 33..33 33 - - - 3517 RMVar_ID_3517 Human_SNP_ID_469735187 A-to-I Human chr11 + 64366274 64366274 64366274 CTCACTGAAATCTCTGCCTCACGGGTTCAAGCAATTCTCCTGCCTTAGCCTCCTGAGTAGTTGGG CTCACTGAAATCTCTGCCTCACGGGTTCAAGCGATTCTCCTGCCTTAGCCTCCTGAGTAGTTGGG A G RPS6KA4 Ensembl:ENSG00000162302 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1485878764 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80658,RMVar_hsa_circ_91794,RMVar_hsa_circ_114325,RMVar_hsa_circ_150474,RMVar_hsa_circ_150476,RMVar_hsa_circ_110858,RMVar_hsa_circ_150475,RMVar_hsa_circ_52007,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 3518 RMVar_ID_3518 Human_SNP_ID_469832282 A-to-I Human chr11 - 64748824 64748824 64748824 GCTGGTCTTGAACTCCTGACCTCAAGTAATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGTTTAC GCTGGTCTTGAACTCCTGACCTCAAGTAATCCTCCCGCCTCGGCCTCCCAAAGTGCTGGGTTTAC T A PYGM Ensembl:ENSG00000068976 Protein coding exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1281612445 Functional Loss SNV dbSNP153 33..33 33 - - - 3519 RMVar_ID_3519 Human_SNP_ID_469832283 A-to-I Human chr11 - 64748829 64748829 64748829 GCCAGGCTGGTCTTGAACTCCTGACCTCAAGTAATCCACCCGCCTCGGCCTCCCAAAGTGCTGGG GCCAGGCTGGTCTTGAACTCCTGACCTCAAGTGATCCACCCGCCTCGGCCTCCCAAAGTGCTGGG T C PYGM Ensembl:ENSG00000068976 Protein coding exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1465807141 Functional Loss SNV dbSNP153 33..33 33 - - - 3520 RMVar_ID_3520 Human_SNP_ID_469852455 A-to-I Human chr11 - 64809751 64809749 64809752 AGGGGGTGTCTCCAGCCGTGAGCTGGTGAAGAAGGTCTCCGATGTCATATGGAACAGCCTCAGCC AGGGGGTGTCTCCAGCCGTGAGCTGGTGAAG___GTCTCCGATGTCATATGGAACAGCCTCAGCC CCTT C MEN1 Ensembl:ENSG00000133895 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs794728657 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_226532,Human_RBP_ID_749546 Human_Splice_Rec_1255417,Human_Splice_Rec_1255449,Human_Splice_Rec_1255467,Human_Splice_Rec_1255485,Human_Splice_Rec_1255501,Human_Splice_Rec_1255519,Human_Splice_Rec_1255593,Human_Splice_Rec_1255609,Human_Splice_Rec_1255629,Human_Splice_Rec_1255645,Human_Splice_Rec_1255661,Human_Splice_Rec_1255677,Human_Splice_Rec_1255685 Clinvar_Rec_29 RMVar_hsa_circ_101503,RMVar_hsa_circ_150514 3521 RMVar_ID_3521 Human_SNP_ID_469867224 A-to-I Human chr11 - 64854739 64854739 64854739 CATCGCGCGGCTGATGGTGATGGTGCGGCAGGAGGAGTCCCTGATGCCTTCCCAGGTGGTCAAGG CATCGCGCGGCTGATGGTGATGGTGCGGCAGGGGGAGTCCCTGATGCCTTCCCAGGTGGTCAAGG T C EHD1 Ensembl:ENSG00000110047 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs768914352 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_865926,Human_RBP_ID_18188271 RMVar_hsa_circ_150517,RMVar_hsa_circ_89553,RMVar_hsa_circ_97999,RMVar_hsa_circ_150518 3522 RMVar_ID_3522 Human_SNP_ID_469868247 A-to-I Human chr11 - 64858310 64858310 64858310 GGGCGTGGTGGTGCGTGCCTGTAATCCCAGCTACTTGGGAGGCTGAGACAGGAGAATCACTTGAA GGGCGTGGTGGTGCGTGCCTGTAATCCCAGCTGCTTGGGAGGCTGAGACAGGAGAATCACTTGAA T C EHD1 Ensembl:ENSG00000110047 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1308542846 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89553,RMVar_hsa_circ_150518 3523 RMVar_ID_3523 Human_SNP_ID_469868272 A-to-I Human chr11 - 64858388 64858388 64858388 CTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGCAAAACCCCATCTCTACTAAAAAAAAT CTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAGCATGGCAAAACCCCATCTCTACTAAAAAAAAT T C EHD1 Ensembl:ENSG00000110047 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1424289376 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89553,RMVar_hsa_circ_150518 3524 RMVar_ID_3524 Human_SNP_ID_469868912 A-to-I Human chr11 - 64860650 64860650 64860650 CGGTGGCATGGGCTTGGCTCACCACAACCTCCACCTGCTGGGTTCAAGCGATTCTCCTGCTTCAG CGGTGGCATGGGCTTGGCTCACCACAACCTCCTCCTGCTGGGTTCAAGCGATTCTCCTGCTTCAG T A EHD1 Ensembl:ENSG00000110047 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7938959 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89553,RMVar_hsa_circ_150518 3525 RMVar_ID_3525 Human_SNP_ID_469868913 A-to-I Human chr11 - 64860650 64860650 64860650 CGGTGGCATGGGCTTGGCTCACCACAACCTCCACCTGCTGGGTTCAAGCGATTCTCCTGCTTCAG CGGTGGCATGGGCTTGGCTCACCACAACCTCCGCCTGCTGGGTTCAAGCGATTCTCCTGCTTCAG T C EHD1 Ensembl:ENSG00000110047 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7938959 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89553,RMVar_hsa_circ_150518 3526 RMVar_ID_3526 Human_SNP_ID_469868914 A-to-I Human chr11 - 64860650 64860650 64860650 CGGTGGCATGGGCTTGGCTCACCACAACCTCCACCTGCTGGGTTCAAGCGATTCTCCTGCTTCAG CGGTGGCATGGGCTTGGCTCACCACAACCTCCCCCTGCTGGGTTCAAGCGATTCTCCTGCTTCAG T G EHD1 Ensembl:ENSG00000110047 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7938959 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89553,RMVar_hsa_circ_150518 3527 RMVar_ID_3527 Human_SNP_ID_469869361 A-to-I Human chr11 - 64862382 64862382 64862382 GTTCATTCTGCTGAAGGAGGCTGGGAAATGCAATCTGAAGCTGGGAGGCCATGAATCCAGCTGAA GTTCATTCTGCTGAAGGAGGCTGGGAAATGCAGTCTGAAGCTGGGAGGCCATGAATCCAGCTGAA T C EHD1 Ensembl:ENSG00000110047 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs3897617 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89553,RMVar_hsa_circ_150518 3528 RMVar_ID_3528 Human_SNP_ID_469869457 A-to-I Human chr11 - 64862840 64862840 64862840 AGACAGGGTGTCGCTCTGTCGCCCAGGCTGGAATGCAGTGGCATGATCACGGCTCACTGCAGCCT AGACAGGGTGTCGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCATGATCACGGCTCACTGCAGCCT T C EHD1 Ensembl:ENSG00000110047 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs186608554 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89553,RMVar_hsa_circ_150518 3529 RMVar_ID_3529 Human_SNP_ID_469872276 A-to-I Human chr11 - 64874156 64874156 64874156 GGGACTACGGGCATGTGCCACCACGCCCGGCTAATTTTTGTATTTTTCGTAGAGATGGGGTTTCA GGGACTACGGGCATGTGCCACCACGCCCGGCTGATTTTTGTATTTTTCGTAGAGATGGGGTTTCA T C EHD1 Ensembl:ENSG00000110047 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1483403859 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89553,RMVar_hsa_circ_150518 3530 RMVar_ID_3530 Human_SNP_ID_469881224 A-to-I Human chr11 - 64904137 64904137 64904137 AGTTCAAGAGATTCTCCTGCCTCAGCCTTCCAAGTAGCTGGGATTACAGGCACCCGCCACCATGC AGTTCAAGAGATTCTCCTGCCTCAGCCTTCCAGGTAGCTGGGATTACAGGCACCCGCCACCATGC T C ATG2A Ensembl:ENSG00000110046 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1199500199 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87532,RMVar_hsa_circ_80252,RMVar_hsa_circ_89734,RMVar_hsa_circ_150521,RMVar_hsa_circ_150522,RMVar_hsa_circ_95835,RMVar_hsa_circ_104637,RMVar_hsa_circ_150523,RMVar_hsa_circ_150524,RMVar_hsa_circ_150525 3531 RMVar_ID_3531 Human_SNP_ID_469914780 A-to-I Human chr11 + 65029184 65029184 65029184 TTTGTGTCGTTGTTTTGTTTTGTTTTTGAGACAGAGTCTCACTGTCGCCCAGACTGGAGTGAAGT TTTGTGTCGTTGTTTTGTTTTGTTTTTGAGACGGAGTCTCACTGTCGCCCAGACTGGAGTGAAGT A G SNX15,ARL2-SNX15 Ensembl:ENSG00000110025,Ensembl:ENSG00000273003 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs961658085 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3377662 3532 RMVar_ID_3532 Human_SNP_ID_469929254 A-to-I Human chr11 - 65081850 65081850 65081850 TCAGCCTCTCAAGTAGCTGGGACTATAGTCACATGCCACCATGCCTGGCTAATTTTTTGATGTTT TCAGCCTCTCAAGTAGCTGGGACTATAGTCACGTGCCACCATGCCTGGCTAATTTTTTGATGTTT T C CDCA5 Ensembl:ENSG00000146670 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1266181004 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121966,RMVar_hsa_circ_150552,RMVar_hsa_circ_78610,RMVar_hsa_circ_150553,RMVar_hsa_circ_71524,RMVar_hsa_circ_17479 3533 RMVar_ID_3533 Human_SNP_ID_469929255 A-to-I Human chr11 - 65081850 65081850 65081850 TCAGCCTCTCAAGTAGCTGGGACTATAGTCACATGCCACCATGCCTGGCTAATTTTTTGATGTTT TCAGCCTCTCAAGTAGCTGGGACTATAGTCACCTGCCACCATGCCTGGCTAATTTTTTGATGTTT T G CDCA5 Ensembl:ENSG00000146670 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1266181004 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121966,RMVar_hsa_circ_150552,RMVar_hsa_circ_78610,RMVar_hsa_circ_150553,RMVar_hsa_circ_71524,RMVar_hsa_circ_17479 3534 RMVar_ID_3534 Human_SNP_ID_469929257 A-to-I Human chr11 - 65081858 65081858 65081858 TTCCCTCCTCAGCCTCTCAAGTAGCTGGGACTATAGTCACATGCCACCATGCCTGGCTAATTTTT TTCCCTCCTCAGCCTCTCAAGTAGCTGGGACTGTAGTCACATGCCACCATGCCTGGCTAATTTTT T C CDCA5 Ensembl:ENSG00000146670 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs111734219 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11668884 RMVar_hsa_circ_121966,RMVar_hsa_circ_150552,RMVar_hsa_circ_78610,RMVar_hsa_circ_150553,RMVar_hsa_circ_71524,RMVar_hsa_circ_17479 3535 RMVar_ID_3535 Human_SNP_ID_469929275 A-to-I Human chr11 - 65081951 65081951 65081951 TAATTCTCTTAGGCCTTACCAGTTCTAAAGATAGGGTCTTGTTCTGCCACCCAGGCTGGAGTGCA TAATTCTCTTAGGCCTTACCAGTTCTAAAGATGGGGTCTTGTTCTGCCACCCAGGCTGGAGTGCA T C CDCA5 Ensembl:ENSG00000146670 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1447228902 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121966,RMVar_hsa_circ_150552,RMVar_hsa_circ_78610,RMVar_hsa_circ_150553,RMVar_hsa_circ_71524,RMVar_hsa_circ_17479 3536 RMVar_ID_3536 Human_SNP_ID_469933811 A-to-I Human chr11 + 65097777 65097777 65097777 TACTCAGGAGACTGAGGAGGGAGGATCACATGAGCCTGGGAGGTCGAGGCTGCAGTGAGCTGTGC TACTCAGGAGACTGAGGAGGGAGGATCACATGGGCCTGGGAGGTCGAGGCTGCAGTGAGCTGTGC A G VPS51 Ensembl:ENSG00000149823 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1358461273 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109635,RMVar_hsa_circ_85671,RMVar_hsa_circ_150560,RMVar_hsa_circ_150561 3537 RMVar_ID_3537 Human_SNP_ID_469933879 A-to-I Human chr11 + 65098130 65098130 65098130 TTGAACCTGGGAGGTGGAGGCTGCGGTGAGCCAAGATCACGTCACTGCACTCCAGCCTAGGCAGC TTGAACCTGGGAGGTGGAGGCTGCGGTGAGCCCAGATCACGTCACTGCACTCCAGCCTAGGCAGC A C VPS51 Ensembl:ENSG00000149823 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs952848826 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109635,RMVar_hsa_circ_85671,RMVar_hsa_circ_150560,RMVar_hsa_circ_150561 3538 RMVar_ID_3538 Human_SNP_ID_469933880 A-to-I Human chr11 + 65098130 65098130 65098130 TTGAACCTGGGAGGTGGAGGCTGCGGTGAGCCAAGATCACGTCACTGCACTCCAGCCTAGGCAGC TTGAACCTGGGAGGTGGAGGCTGCGGTGAGCCGAGATCACGTCACTGCACTCCAGCCTAGGCAGC A G VPS51 Ensembl:ENSG00000149823 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs952848826 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109635,RMVar_hsa_circ_85671,RMVar_hsa_circ_150560,RMVar_hsa_circ_150561 3539 RMVar_ID_3539 Human_SNP_ID_469934249 A-to-I Human chr11 + 65099845 65099845 65099845 AATAAAAAGGCCAGGTGCGGTGGCTTATGCCTATAATCTTAGCACTCTGAGAGGCCGAGACGGGT AATAAAAAGGCCAGGTGCGGTGGCTTATGCCTGTAATCTTAGCACTCTGAGAGGCCGAGACGGGT A G VPS51 Ensembl:ENSG00000149823 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs906737921 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109635,RMVar_hsa_circ_85671,RMVar_hsa_circ_150560,RMVar_hsa_circ_150561 3540 RMVar_ID_3540 Human_SNP_ID_469934281 A-to-I Human chr11 + 65099992 65099992 65099992 AGGCATGGTGGCAGGCATCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAA AGGCATGGTGGCAGGCATCTGTAGTCCCAGCTGCTCAGGAGGCTGAGGCAGGAGAATCGCTTGAA A G VPS51 Ensembl:ENSG00000149823 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965151739 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_109186 RMVar_hsa_circ_109635,RMVar_hsa_circ_85671,RMVar_hsa_circ_150560,RMVar_hsa_circ_150561 3541 RMVar_ID_3541 Human_SNP_ID_469934817 A-to-I Human chr11 + 65102187 65102187 65102187 TTACAGGCACCTGCCACCACACTTGGCTAATTATTGTATTTTCAGTAGAGACGGGATTTCACCAT TTACAGGCACCTGCCACCACACTTGGCTAATTGTTGTATTTTCAGTAGAGACGGGATTTCACCAT A G VPS51 Ensembl:ENSG00000149823 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs867682529 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109635,RMVar_hsa_circ_85671,RMVar_hsa_circ_150560,RMVar_hsa_circ_150561 3542 RMVar_ID_3542 Human_SNP_ID_469934818 A-to-I Human chr11 + 65102192 65102192 65102192 GGCACCTGCCACCACACTTGGCTAATTATTGTATTTTCAGTAGAGACGGGATTTCACCATGTTGG GGCACCTGCCACCACACTTGGCTAATTATTGTGTTTTCAGTAGAGACGGGATTTCACCATGTTGG A G VPS51 Ensembl:ENSG00000149823 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1297264674 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109635,RMVar_hsa_circ_85671,RMVar_hsa_circ_150560,RMVar_hsa_circ_150561 3543 RMVar_ID_3543 Human_SNP_ID_469935415 A-to-I Human chr11 + 65105238 65105238 65105238 AACATGGTGAAACCCTCTCTACTAAAAGTACAAAAATTAGCCAGGCATGGTGGCACGTGCCTGTA AACATGGTGAAACCCTCTCTACTAAAAGTACACAAATTAGCCAGGCATGGTGGCACGTGCCTGTA A C VPS51 Ensembl:ENSG00000149823 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1388106043 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109635,RMVar_hsa_circ_85671,RMVar_hsa_circ_150560,RMVar_hsa_circ_150561 3544 RMVar_ID_3544 Human_SNP_ID_469935418 A-to-I Human chr11 + 65105252 65105252 65105252 CTCTCTACTAAAAGTACAAAAATTAGCCAGGCATGGTGGCACGTGCCTGTAATCCCAGCTACTCG CTCTCTACTAAAAGTACAAAAATTAGCCAGGCGTGGTGGCACGTGCCTGTAATCCCAGCTACTCG A G VPS51 Ensembl:ENSG00000149823 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs903712497 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109635,RMVar_hsa_circ_85671,RMVar_hsa_circ_150560,RMVar_hsa_circ_150561 3545 RMVar_ID_3545 Human_SNP_ID_469941857 A-to-I Human chr11 + 65123457 65123457 65123457 GAAGACAAAGGTTTTTAACAGAAAAATGGGCCAGGCACGGTGGCTCACGCCTGTAATCCCAGCAC GAAGACAAAGGTTTTTAACAGAAAAATGGGCCGGGCACGGTGGCTCACGCCTGTAATCCCAGCAC A G MRPL49 Ensembl:ENSG00000149792 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs926129662 Functional Loss SNV dbSNP153 33..33 33 - - - 3546 RMVar_ID_3546 Human_SNP_ID_469941906 A-to-I Human chr11 + 65123613 65123613 65123613 AAAATTAGCCGGGTGTGATGGCGTGTGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGTAGGAGA AAAATTAGCCGGGTGTGATGGCGTGTGCCTGTCGTCCCAGCTACTTGGGAGGCTGAGGTAGGAGA A C MRPL49 Ensembl:ENSG00000149792 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1001628612 Functional Loss SNV dbSNP153 33..33 33 - - - 3547 RMVar_ID_3547 Human_SNP_ID_469956276 A-to-I Human chr11 - 65180254 65180254 65180254 CTCTCACCTCAGCCTCCTGAGTAGCTGAGACTACAGGCACGTGCCACGACACACAGCTAATTTTT CTCTCACCTCAGCCTCCTGAGTAGCTGAGACTGCAGGCACGTGCCACGACACACAGCTAATTTTT T C AP003068.2 Ensembl:ENSG00000254614 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1365854690 Functional Loss SNV dbSNP153 33..33 33 - - - 3548 RMVar_ID_3548 Human_SNP_ID_469968375 A-to-I Human chr11 + 65226397 65226374 65226397 GTGGGGTCTTGCAATGTCGCCCAGGCTGGTCTAGAACTCCTGGACTGAAGCGATCCTCCCCCTTG GTGGGGTCTT_______________________GAACTCCTGGACTGAAGCGATCCTCCCCCTTG TGCAATGTCGCCCAGGCTGGTCTA T SLC22A20P Ensembl:ENSG00000197847 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs995580734 Functional Loss DEL dbSNP153 11..33 33 - - - 3549 RMVar_ID_3549 Human_SNP_ID_469978516 A-to-I Human chr11 + 65263283 65263282 65263284 GTTTTATCACCCAGGCTGGAGTGCAGTGGTGCAATCTCGGCTCACTTCAGCCTCCGCCTCCCAGG GTTTTATCACCCAGGCTGGAGTGCAGTGGTGC__TCTCGGCTCACTTCAGCCTCCGCCTCCCAGG CAA C AP000944.5,POLA2 Ensembl:ENSG00000285816,Ensembl:ENSG00000014138 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1435129958 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_85792,RMVar_hsa_circ_108397,RMVar_hsa_circ_96374,RMVar_hsa_circ_150604,RMVar_hsa_circ_150605,RMVar_hsa_circ_150603 3550 RMVar_ID_3550 Human_SNP_ID_469978561 A-to-I Human chr11 + 65263428 65263428 65263428 GTACTTTTAGTAGAGAAGGGGTTTCACCATGTAGGCCAGACTGCTCTCGAACTCCTGACCTCAAG GTACTTTTAGTAGAGAAGGGGTTTCACCATGTGGGCCAGACTGCTCTCGAACTCCTGACCTCAAG A G AP000944.5,POLA2 Ensembl:ENSG00000285816,Ensembl:ENSG00000014138 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs996778632 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11669763 RMVar_hsa_circ_85792,RMVar_hsa_circ_108397,RMVar_hsa_circ_96374,RMVar_hsa_circ_150604,RMVar_hsa_circ_150605,RMVar_hsa_circ_150603 3551 RMVar_ID_3551 Human_SNP_ID_469978589 A-to-I Human chr11 + 65263572 65263572 65263572 AAGACTAGCCAGGTGTGGTGGCTCACGCCTGTAATCCCAGCATTTTGGGAGGCCAAGGCAGGTGG AAGACTAGCCAGGTGTGGTGGCTCACGCCTGTCATCCCAGCATTTTGGGAGGCCAAGGCAGGTGG A C AP000944.5,POLA2 Ensembl:ENSG00000285816,Ensembl:ENSG00000014138 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1485155805 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85792,RMVar_hsa_circ_108397,RMVar_hsa_circ_96374,RMVar_hsa_circ_150604,RMVar_hsa_circ_150605,RMVar_hsa_circ_150603 3552 RMVar_ID_3552 Human_SNP_ID_469980552 A-to-I Human chr11 + 65271716 65271716 65271716 CAAAAAATTAGCTGGGCATGGTGGTGGTGCCTATAATCCCAGCCACTCAGGAGGCTGAGGCAGGA CAAAAAATTAGCTGGGCATGGTGGTGGTGCCTGTAATCCCAGCCACTCAGGAGGCTGAGGCAGGA A G AP000944.5,POLA2 Ensembl:ENSG00000285816,Ensembl:ENSG00000014138 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs184487612 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25259,RMVar_hsa_circ_85792,RMVar_hsa_circ_96374,RMVar_hsa_circ_150604,RMVar_hsa_circ_150603,RMVar_hsa_circ_61956,RMVar_hsa_circ_341351 3553 RMVar_ID_3553 Human_SNP_ID_469983189 A-to-I Human chr11 + 65282947 65282947 65282947 GGCCAGGAGTTGGAAACTAGCCTGGGCAACATAGGGAGACCCTGTCTCTACTAAAAATTAAAAAA GGCCAGGAGTTGGAAACTAGCCTGGGCAACATGGGGAGACCCTGTCTCTACTAAAAATTAAAAAA A G AP000944.5,POLA2 Ensembl:ENSG00000285816,Ensembl:ENSG00000014138 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs596357 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85792,RMVar_hsa_circ_96374,RMVar_hsa_circ_150604,RMVar_hsa_circ_150603,RMVar_hsa_circ_61956,RMVar_hsa_circ_88335,RMVar_hsa_circ_115010,RMVar_hsa_circ_373934,RMVar_hsa_circ_150609,RMVar_hsa_circ_150610,RMVar_hsa_circ_43816,RMVar_hsa_circ_80024,RMVar_hsa_circ_150611,RMVar_hsa_circ_150614,RMVar_hsa_circ_21112,RMVar_hsa_circ_150613,RMVar_hsa_circ_150615,RMVar_hsa_circ_371819 3554 RMVar_ID_3554 Human_SNP_ID_469983323 A-to-I Human chr11 + 65283544 65283544 65283544 CAGGCTGGAGTGCAGTGGCAAGATCTTGGCTCACTGCAAGCTCCGCCTCCCGGGTTCAGGTGATT CAGGCTGGAGTGCAGTGGCAAGATCTTGGCTCGCTGCAAGCTCCGCCTCCCGGGTTCAGGTGATT A G AP000944.5,POLA2 Ensembl:ENSG00000285816,Ensembl:ENSG00000014138 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs986529791 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85792,RMVar_hsa_circ_96374,RMVar_hsa_circ_150604,RMVar_hsa_circ_150603,RMVar_hsa_circ_61956,RMVar_hsa_circ_88335,RMVar_hsa_circ_115010,RMVar_hsa_circ_373934,RMVar_hsa_circ_150609,RMVar_hsa_circ_150610,RMVar_hsa_circ_43816,RMVar_hsa_circ_80024,RMVar_hsa_circ_150611,RMVar_hsa_circ_150614,RMVar_hsa_circ_21112,RMVar_hsa_circ_150613,RMVar_hsa_circ_150615,RMVar_hsa_circ_371819 3555 RMVar_ID_3555 Human_SNP_ID_469983332 A-to-I Human chr11 + 65283569 65283569 65283569 TTGGCTCACTGCAAGCTCCGCCTCCCGGGTTCAGGTGATTCTCCTGCCTCAGCCTCCTAAGTAGC TTGGCTCACTGCAAGCTCCGCCTCCCGGGTTCGGGTGATTCTCCTGCCTCAGCCTCCTAAGTAGC A G AP000944.5,POLA2 Ensembl:ENSG00000285816,Ensembl:ENSG00000014138 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1176400156 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85792,RMVar_hsa_circ_96374,RMVar_hsa_circ_150604,RMVar_hsa_circ_150603,RMVar_hsa_circ_61956,RMVar_hsa_circ_88335,RMVar_hsa_circ_115010,RMVar_hsa_circ_373934,RMVar_hsa_circ_150609,RMVar_hsa_circ_150610,RMVar_hsa_circ_43816,RMVar_hsa_circ_80024,RMVar_hsa_circ_150611,RMVar_hsa_circ_150614,RMVar_hsa_circ_21112,RMVar_hsa_circ_150613,RMVar_hsa_circ_150615,RMVar_hsa_circ_371819 3556 RMVar_ID_3556 Human_SNP_ID_469983447 A-to-I Human chr11 + 65284073 65284073 65284073 CGGGGATCACTTGAGCCTGGGAAGTCAAGGCTACAGTAAGCCGTGATCATGCCACTGCACTTCAG CGGGGATCACTTGAGCCTGGGAAGTCAAGGCTGCAGTAAGCCGTGATCATGCCACTGCACTTCAG A G AP000944.5,POLA2 Ensembl:ENSG00000285816,Ensembl:ENSG00000014138 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1410494969 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85792,RMVar_hsa_circ_96374,RMVar_hsa_circ_150604,RMVar_hsa_circ_150603,RMVar_hsa_circ_61956,RMVar_hsa_circ_88335,RMVar_hsa_circ_115010,RMVar_hsa_circ_373934,RMVar_hsa_circ_150609,RMVar_hsa_circ_150610,RMVar_hsa_circ_43816,RMVar_hsa_circ_80024,RMVar_hsa_circ_150611,RMVar_hsa_circ_150614,RMVar_hsa_circ_21112,RMVar_hsa_circ_150613,RMVar_hsa_circ_150615,RMVar_hsa_circ_371819 3557 RMVar_ID_3557 Human_SNP_ID_469983530 A-to-I Human chr11 + 65284423 65284423 65284423 AGGATTGCTTGAGCCCAGGAAGTCAAGGCTGCAGTGAGCCATGATTGTGCCATTGCACTCCAGCC AGGATTGCTTGAGCCCAGGAAGTCAAGGCTGCCGTGAGCCATGATTGTGCCATTGCACTCCAGCC A C AP000944.5,POLA2 Ensembl:ENSG00000285816,Ensembl:ENSG00000014138 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs932874754 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85792,RMVar_hsa_circ_96374,RMVar_hsa_circ_150604,RMVar_hsa_circ_150603,RMVar_hsa_circ_61956,RMVar_hsa_circ_88335,RMVar_hsa_circ_115010,RMVar_hsa_circ_373934,RMVar_hsa_circ_150609,RMVar_hsa_circ_150610,RMVar_hsa_circ_43816,RMVar_hsa_circ_80024,RMVar_hsa_circ_150611,RMVar_hsa_circ_150614,RMVar_hsa_circ_21112,RMVar_hsa_circ_150613,RMVar_hsa_circ_150615,RMVar_hsa_circ_371819 3558 RMVar_ID_3558 Human_SNP_ID_469983611 A-to-I Human chr11 + 65284692 65284692 65284692 GGATTACAGGCATGCACCTGTAATGCCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCT GGATTACAGGCATGCACCTGTAATGCCTGGCTGATTTTTGTATTTTTAGTAGAGATGGGGTTTCT A G AP000944.5,POLA2 Ensembl:ENSG00000285816,Ensembl:ENSG00000014138 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1309721661 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85792,RMVar_hsa_circ_96374,RMVar_hsa_circ_150604,RMVar_hsa_circ_150603,RMVar_hsa_circ_61956,RMVar_hsa_circ_88335,RMVar_hsa_circ_115010,RMVar_hsa_circ_373934,RMVar_hsa_circ_150609,RMVar_hsa_circ_150610,RMVar_hsa_circ_43816,RMVar_hsa_circ_80024,RMVar_hsa_circ_150611,RMVar_hsa_circ_150614,RMVar_hsa_circ_21112,RMVar_hsa_circ_150613,RMVar_hsa_circ_150615,RMVar_hsa_circ_371819 3559 RMVar_ID_3559 Human_SNP_ID_469983614 A-to-I Human chr11 + 65284710 65284710 65284710 TGTAATGCCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCTCCATGTTGGTCAGGCTGG TGTAATGCCTGGCTAATTTTTGTATTTTTAGTGGAGATGGGGTTTCTCCATGTTGGTCAGGCTGG A G AP000944.5,POLA2 Ensembl:ENSG00000285816,Ensembl:ENSG00000014138 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1365550142 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85792,RMVar_hsa_circ_96374,RMVar_hsa_circ_150604,RMVar_hsa_circ_150603,RMVar_hsa_circ_61956,RMVar_hsa_circ_88335,RMVar_hsa_circ_115010,RMVar_hsa_circ_373934,RMVar_hsa_circ_150609,RMVar_hsa_circ_150610,RMVar_hsa_circ_43816,RMVar_hsa_circ_80024,RMVar_hsa_circ_150611,RMVar_hsa_circ_150614,RMVar_hsa_circ_21112,RMVar_hsa_circ_150613,RMVar_hsa_circ_150615,RMVar_hsa_circ_371819 3560 RMVar_ID_3560 Human_SNP_ID_469983730 A-to-I Human chr11 + 65285239 65285239 65285239 CATTCTGGCCAACAAGCTGAAACCCCATCTCCACTAAAAAATACAAAAATTAGCTTGGCTTGGCA CATTCTGGCCAACAAGCTGAAACCCCATCTCCCCTAAAAAATACAAAAATTAGCTTGGCTTGGCA A C AP000944.5,POLA2 Ensembl:ENSG00000285816,Ensembl:ENSG00000014138 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1442876582 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85792,RMVar_hsa_circ_96374,RMVar_hsa_circ_150604,RMVar_hsa_circ_150603,RMVar_hsa_circ_61956,RMVar_hsa_circ_88335,RMVar_hsa_circ_115010,RMVar_hsa_circ_373934,RMVar_hsa_circ_150609,RMVar_hsa_circ_150610,RMVar_hsa_circ_43816,RMVar_hsa_circ_80024,RMVar_hsa_circ_150611,RMVar_hsa_circ_150614,RMVar_hsa_circ_21112,RMVar_hsa_circ_150613,RMVar_hsa_circ_150615,RMVar_hsa_circ_371819 3561 RMVar_ID_3561 Human_SNP_ID_469983740 A-to-I Human chr11 + 65285282 65285282 65285282 CAAAAATTAGCTTGGCTTGGCAGCGTGTGCCTATAATCCCAGTTACTCAGGAGGCTGAGGCAGGA CAAAAATTAGCTTGGCTTGGCAGCGTGTGCCTGTAATCCCAGTTACTCAGGAGGCTGAGGCAGGA A G AP000944.5,POLA2 Ensembl:ENSG00000285816,Ensembl:ENSG00000014138 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1471426866 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85792,RMVar_hsa_circ_96374,RMVar_hsa_circ_150604,RMVar_hsa_circ_150603,RMVar_hsa_circ_61956,RMVar_hsa_circ_88335,RMVar_hsa_circ_115010,RMVar_hsa_circ_373934,RMVar_hsa_circ_150609,RMVar_hsa_circ_150610,RMVar_hsa_circ_43816,RMVar_hsa_circ_80024,RMVar_hsa_circ_150611,RMVar_hsa_circ_150614,RMVar_hsa_circ_21112,RMVar_hsa_circ_150613,RMVar_hsa_circ_150615,RMVar_hsa_circ_371819 3562 RMVar_ID_3562 Human_SNP_ID_469983753 A-to-I Human chr11 + 65285337 65285337 65285337 TGAGGCAGGAGAATCGCTTGAACCTGGGAGGTAGAAGTTGCAGTGAGCCGAGATCGCCAATGAAC TGAGGCAGGAGAATCGCTTGAACCTGGGAGGTGGAAGTTGCAGTGAGCCGAGATCGCCAATGAAC A G AP000944.5,POLA2 Ensembl:ENSG00000285816,Ensembl:ENSG00000014138 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs949074853 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11670296 RMVar_hsa_circ_85792,RMVar_hsa_circ_96374,RMVar_hsa_circ_150604,RMVar_hsa_circ_150603,RMVar_hsa_circ_61956,RMVar_hsa_circ_88335,RMVar_hsa_circ_115010,RMVar_hsa_circ_373934,RMVar_hsa_circ_150609,RMVar_hsa_circ_150610,RMVar_hsa_circ_43816,RMVar_hsa_circ_80024,RMVar_hsa_circ_150611,RMVar_hsa_circ_150614,RMVar_hsa_circ_21112,RMVar_hsa_circ_150613,RMVar_hsa_circ_150615,RMVar_hsa_circ_371819 3563 RMVar_ID_3563 Human_SNP_ID_469983795 A-to-I Human chr11 + 65285514 65285514 65285514 CACTCTCCTGAGTCCAGGAGTTCAAGGCTGCCATGAGCCATGATCATACCACTACTGCACTCCAG CACTCTCCTGAGTCCAGGAGTTCAAGGCTGCCGTGAGCCATGATCATACCACTACTGCACTCCAG A G AP000944.5,POLA2 Ensembl:ENSG00000285816,Ensembl:ENSG00000014138 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1202535475 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11670300,Human_RBP_ID_24895384 RMVar_hsa_circ_85792,RMVar_hsa_circ_96374,RMVar_hsa_circ_150604,RMVar_hsa_circ_150603,RMVar_hsa_circ_61956,RMVar_hsa_circ_88335,RMVar_hsa_circ_115010,RMVar_hsa_circ_373934,RMVar_hsa_circ_150609,RMVar_hsa_circ_150610,RMVar_hsa_circ_43816,RMVar_hsa_circ_80024,RMVar_hsa_circ_150611,RMVar_hsa_circ_150614,RMVar_hsa_circ_21112,RMVar_hsa_circ_150613,RMVar_hsa_circ_150615,RMVar_hsa_circ_371819 3564 RMVar_ID_3564 Human_SNP_ID_469984527 A-to-I Human chr11 + 65288589 65288589 65288589 GCTGGAGTGCTGTGGTGCGATCTCGGCTCACTATAGCCTCCACCTCCTGGGCTCAAGTGAGCCTC GCTGGAGTGCTGTGGTGCGATCTCGGCTCACTGTAGCCTCCACCTCCTGGGCTCAAGTGAGCCTC A G AP000944.5,POLA2 Ensembl:ENSG00000285816,Ensembl:ENSG00000014138 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs372078726 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24895408 RMVar_hsa_circ_85792,RMVar_hsa_circ_96374,RMVar_hsa_circ_150604,RMVar_hsa_circ_150603,RMVar_hsa_circ_61956,RMVar_hsa_circ_88335,RMVar_hsa_circ_115010,RMVar_hsa_circ_373934,RMVar_hsa_circ_150609,RMVar_hsa_circ_150610,RMVar_hsa_circ_43816,RMVar_hsa_circ_80024,RMVar_hsa_circ_150611,RMVar_hsa_circ_150614,RMVar_hsa_circ_21112,RMVar_hsa_circ_150613,RMVar_hsa_circ_150616,RMVar_hsa_circ_295786,RMVar_hsa_circ_150615,RMVar_hsa_circ_371819,RMVar_hsa_circ_315105,RMVar_hsa_circ_150617 3565 RMVar_ID_3565 Human_SNP_ID_469984553 A-to-I Human chr11 + 65288703 65288703 65288703 ACCATGCCCAACTAATTTTTGTATTTTTTTGTAGAGAGAGGGTTTCACCATATTGCCCAGGCTAG ACCATGCCCAACTAATTTTTGTATTTTTTTGTGGAGAGAGGGTTTCACCATATTGCCCAGGCTAG A G AP000944.5,POLA2 Ensembl:ENSG00000285816,Ensembl:ENSG00000014138 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs952749189 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85792,RMVar_hsa_circ_96374,RMVar_hsa_circ_150604,RMVar_hsa_circ_150603,RMVar_hsa_circ_61956,RMVar_hsa_circ_88335,RMVar_hsa_circ_115010,RMVar_hsa_circ_373934,RMVar_hsa_circ_150609,RMVar_hsa_circ_150610,RMVar_hsa_circ_43816,RMVar_hsa_circ_80024,RMVar_hsa_circ_150611,RMVar_hsa_circ_150614,RMVar_hsa_circ_21112,RMVar_hsa_circ_150613,RMVar_hsa_circ_150616,RMVar_hsa_circ_295786,RMVar_hsa_circ_150615,RMVar_hsa_circ_371819,RMVar_hsa_circ_315105,RMVar_hsa_circ_150617 3566 RMVar_ID_3566 Human_SNP_ID_469986443 A-to-I Human chr11 + 65296808 65296808 65296808 ATCTCTACTAAAAATACAAAAATTAGCCAGGCATGGTGGTGTGGGTGCCTGTAATCCAAGCTACC ATCTCTACTAAAAATACAAAAATTAGCCAGGCGTGGTGGTGTGGGTGCCTGTAATCCAAGCTACC A G AP000944.5,POLA2 Ensembl:ENSG00000285816,Ensembl:ENSG00000014138 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1258053949 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88335,RMVar_hsa_circ_150611,RMVar_hsa_circ_97700,RMVar_hsa_circ_150622 3567 RMVar_ID_3567 Human_SNP_ID_469986745 A-to-I Human chr11 + 65297902 65297902 65297902 TCGATCTCCTGACCTTGTGATCTGTCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG TCGATCTCCTGACCTTGTGATCTGTCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG A G AP000944.5,POLA2 Ensembl:ENSG00000285816,Ensembl:ENSG00000014138 Protein coding,Protein coding intron,3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs368468609 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1394283 3568 RMVar_ID_3568 Human_SNP_ID_469987160 A-to-I Human chr11 + 65299723 65299695 65299723 TCACTCCACCAACCCCACCCCGACAGAGTCTCACTCTGTCGTCCGGGCTGGAGTGCAGTGGCGCG TCACT____________________________CTCTGTCGTCCGGGCTGGAGTGCAGTGGCGCG TCCACCAACCCCACCCCGACAGAGTCTCA T AP000944.5,POLA2 Ensembl:ENSG00000285816,Ensembl:ENSG00000014138 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1472855082 Functional Loss DEL dbSNP153 6..33 33 - - - Human_RBP_ID_11670554 3569 RMVar_ID_3569 Human_SNP_ID_469988867 A-to-I Human chr11 + 65306669 65306669 65306669 ATTACCTCAGCCAGGCGCTTTGGCTCACCCTTATAACCCCAGCACTTTGGGAGGCCGAGGCAGAT ATTACCTCAGCCAGGCGCTTTGGCTCACCCTTGTAACCCCAGCACTTTGGGAGGCCGAGGCAGAT A G AP000944.5 Ensembl:ENSG00000285816 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs536200882 Functional Loss SNV dbSNP153 33..33 33 - - - 3570 RMVar_ID_3570 Human_SNP_ID_469993196 A-to-I Human chr11 + 65323774 65323774 65323774 GAACTTCTGACCCCAGTTGATCCGCCCGCCTCAGCCTCCCAAAGTGCTGGTATTACAGGCATGAG GAACTTCTGACCCCAGTTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGTATTACAGGCATGAG A G AP000944.5 Ensembl:ENSG00000285816 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006199529 Functional Loss SNV dbSNP153 33..33 33 - - - 3571 RMVar_ID_3571 Human_SNP_ID_469993201 A-to-I Human chr11 + 65323802 65323785 65323802 CCTCAGCCTCCCAAAGTGCTGGTATTACAGGCATGAGCCACCATGCCCGTCCAGGAAAGGTGTTA CCTCAGCCTCCCAAAG_________________TGAGCCACCATGCCCGTCCAGGAAAGGTGTTA GTGCTGGTATTACAGGCA G AP000944.5 Ensembl:ENSG00000285816 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1191035504 Functional Loss DEL dbSNP153 17..33 33 - - - 3572 RMVar_ID_3572 Human_SNP_ID_469996616 A-to-I Human chr11 + 65335835 65335834 65335836 CTCATCTTTTCTTTTTTTTTATTTTTTTAGACAGAGTCTCACTGTTGTCGGCCCGGGCTGGAATG CTCATCTTTTCTTTTTTTTTATTTTTTTAGAC__AGTCTCACTGTTGTCGGCCCGGGCTGGAATG CAG C DPF2 Ensembl:ENSG00000133884 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1338664418 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_118217,RMVar_hsa_circ_150625 3573 RMVar_ID_3573 Human_SNP_ID_469996621 A-to-I Human chr11 + 65335843 65335843 65335843 TTCTTTTTTTTTATTTTTTTAGACAGAGTCTCACTGTTGTCGGCCCGGGCTGGAATGCAGTGGCA TTCTTTTTTTTTATTTTTTTAGACAGAGTCTCCCTGTTGTCGGCCCGGGCTGGAATGCAGTGGCA A C DPF2 Ensembl:ENSG00000133884 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs898405477 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118217,RMVar_hsa_circ_150625 3574 RMVar_ID_3574 Human_SNP_ID_469997511 A-to-I Human chr11 + 65337970 65337970 65337970 GGGATTATGGTCATGTACCACCACGCCCGGCTAATTTTGTATTTTTAGTAGAGACAGGGTTTCTC GGGATTATGGTCATGTACCACCACGCCCGGCTTATTTTGTATTTTTAGTAGAGACAGGGTTTCTC A T DPF2 Ensembl:ENSG00000133884 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1275105398 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118217,RMVar_hsa_circ_150625 3575 RMVar_ID_3575 Human_SNP_ID_470000021 A-to-I Human chr11 + 65347399 65347399 65347399 TCATCCAGGCTGGAGTGCAGTGACGCGATCTTAGCTCACTAAAACCTTTCCCTTCAGGCTCAAGC TCATCCAGGCTGGAGTGCAGTGACGCGATCTTGGCTCACTAAAACCTTTCCCTTCAGGCTCAAGC A G DPF2 Ensembl:ENSG00000133884 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1249018341 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41495,RMVar_hsa_circ_118217,RMVar_hsa_circ_150625,RMVar_hsa_circ_77563,RMVar_hsa_circ_79877,RMVar_hsa_circ_85591,RMVar_hsa_circ_150626,RMVar_hsa_circ_150627,RMVar_hsa_circ_107278,RMVar_hsa_circ_150629,RMVar_hsa_circ_150630 3576 RMVar_ID_3576 Human_SNP_ID_470000054 A-to-I Human chr11 + 65347554 65347554 65347554 ACAGGGTCTTGCCATATTGCTGAGCTGGTCTCAAACTCCTGAGCTCAAGCAGTCCTCCCACCTTG ACAGGGTCTTGCCATATTGCTGAGCTGGTCTCCAACTCCTGAGCTCAAGCAGTCCTCCCACCTTG A C DPF2 Ensembl:ENSG00000133884 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1373592207 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41495,RMVar_hsa_circ_118217,RMVar_hsa_circ_150625,RMVar_hsa_circ_77563,RMVar_hsa_circ_79877,RMVar_hsa_circ_85591,RMVar_hsa_circ_150626,RMVar_hsa_circ_150627,RMVar_hsa_circ_107278,RMVar_hsa_circ_150629,RMVar_hsa_circ_150630 3577 RMVar_ID_3577 Human_SNP_ID_470000200 A-to-I Human chr11 + 65348164 65348164 65348164 AACACTTAGCCAGGTGTGGTGGCACACACGTTAGTCCCAGCTACTTGGCAGGCTGAGGTGGGAGG AACACTTAGCCAGGTGTGGTGGCACACACGTTTGTCCCAGCTACTTGGCAGGCTGAGGTGGGAGG A T DPF2 Ensembl:ENSG00000133884 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs560779236 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41495,RMVar_hsa_circ_118217,RMVar_hsa_circ_150625,RMVar_hsa_circ_77563,RMVar_hsa_circ_79877,RMVar_hsa_circ_85591,RMVar_hsa_circ_150626,RMVar_hsa_circ_150627,RMVar_hsa_circ_107278,RMVar_hsa_circ_150629,RMVar_hsa_circ_150630 3578 RMVar_ID_3578 Human_SNP_ID_470000266 A-to-I Human chr11 + 65348458 65348458 65348458 GAAAAATTAGCTAGGTGTGGTGGTGTGTGCCTATAGTCCCAGCTACTTGAGAGGCTGAGGTAGGA GAAAAATTAGCTAGGTGTGGTGGTGTGTGCCTGTAGTCCCAGCTACTTGAGAGGCTGAGGTAGGA A G DPF2 Ensembl:ENSG00000133884 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1350603897 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41495,RMVar_hsa_circ_118217,RMVar_hsa_circ_150625,RMVar_hsa_circ_77563,RMVar_hsa_circ_79877,RMVar_hsa_circ_85591,RMVar_hsa_circ_150626,RMVar_hsa_circ_150627,RMVar_hsa_circ_107278,RMVar_hsa_circ_150629,RMVar_hsa_circ_150630 3579 RMVar_ID_3579 Human_SNP_ID_470000268 A-to-I Human chr11 + 65348460 65348460 65348460 AAAATTAGCTAGGTGTGGTGGTGTGTGCCTATAGTCCCAGCTACTTGAGAGGCTGAGGTAGGAGG AAAATTAGCTAGGTGTGGTGGTGTGTGCCTATGGTCCCAGCTACTTGAGAGGCTGAGGTAGGAGG A G DPF2 Ensembl:ENSG00000133884 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1242803597 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41495,RMVar_hsa_circ_118217,RMVar_hsa_circ_150625,RMVar_hsa_circ_77563,RMVar_hsa_circ_79877,RMVar_hsa_circ_85591,RMVar_hsa_circ_150626,RMVar_hsa_circ_150627,RMVar_hsa_circ_107278,RMVar_hsa_circ_150629,RMVar_hsa_circ_150630 3580 RMVar_ID_3580 Human_SNP_ID_470000796 A-to-I Human chr11 + 65350436 65350436 65350436 TTGTTCTGTTGCCCATGTTGGAGTGGAGTGGCATGATCTCAGCTCACTGCAACCTCTGCTTCCCC TTGTTCTGTTGCCCATGTTGGAGTGGAGTGGCGTGATCTCAGCTCACTGCAACCTCTGCTTCCCC A G DPF2 Ensembl:ENSG00000133884 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs892556199 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17560366 RMVar_hsa_circ_118217,RMVar_hsa_circ_150625,RMVar_hsa_circ_77563,RMVar_hsa_circ_79877,RMVar_hsa_circ_85591,RMVar_hsa_circ_150626,RMVar_hsa_circ_150627,RMVar_hsa_circ_107278,RMVar_hsa_circ_150629,RMVar_hsa_circ_150630 3581 RMVar_ID_3581 Human_SNP_ID_470000798 A-to-I Human chr11 + 65350439 65350439 65350439 TTCTGTTGCCCATGTTGGAGTGGAGTGGCATGATCTCAGCTCACTGCAACCTCTGCTTCCCCGGG TTCTGTTGCCCATGTTGGAGTGGAGTGGCATGTTCTCAGCTCACTGCAACCTCTGCTTCCCCGGG A T DPF2 Ensembl:ENSG00000133884 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs552752850 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17560366 RMVar_hsa_circ_118217,RMVar_hsa_circ_150625,RMVar_hsa_circ_77563,RMVar_hsa_circ_79877,RMVar_hsa_circ_85591,RMVar_hsa_circ_150626,RMVar_hsa_circ_150627,RMVar_hsa_circ_107278,RMVar_hsa_circ_150629,RMVar_hsa_circ_150630 3582 RMVar_ID_3582 Human_SNP_ID_470006518 A-to-I Human chr11 - 65371771 65371771 65371771 TCTCTACTAAAAATACAAAAAATTAGCCGGGCATGGTGGCACGCACCTGTAGTCACAGTTACTTG TCTCTACTAAAAATACAAAAAATTAGCCGGGCTTGGTGGCACGCACCTGTAGTCACAGTTACTTG T A L13304-001,L13705-009 RNACentral:URS000044B5AA,RNACentral:URS00001E2917 scRNA,misc_RNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs551233005 Functional Loss SNV dbSNP153 33..33 33 - - - 3583 RMVar_ID_3583 Human_SNP_ID_470006519 A-to-I Human chr11 - 65371771 65371771 65371771 TCTCTACTAAAAATACAAAAAATTAGCCGGGCATGGTGGCACGCACCTGTAGTCACAGTTACTTG TCTCTACTAAAAATACAAAAAATTAGCCGGGCGTGGTGGCACGCACCTGTAGTCACAGTTACTTG T C L13304-001,L13705-009 RNACentral:URS000044B5AA,RNACentral:URS00001E2917 scRNA,misc_RNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs551233005 Functional Loss SNV dbSNP153 33..33 33 - - - 3584 RMVar_ID_3584 Human_SNP_ID_470006992 A-to-I Human chr11 - 65373765 65373765 65373765 TGGGCAACATAGTGAGACCTTGTATCTACCAAAAATTTAAACATTAGCCAGGTGTGGTGGCACTG TGGGCAACATAGTGAGACCTTGTATCTACCAAGAATTTAAACATTAGCCAGGTGTGGTGGCACTG T C L13304-001,L13705-009 RNACentral:URS000044B5AA,RNACentral:URS00001E2917 scRNA,misc_RNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs933780741 Functional Loss SNV dbSNP153 33..33 33 - - - 3585 RMVar_ID_3585 Human_SNP_ID_470007001 A-to-I Human chr11 - 65373806 65373806 65373806 AGGCAGGAGGACCACTTGAGGCTAGGAGTTCAAGACCAGCCTGGGCAACATAGTGAGACCTTGTA AGGCAGGAGGACCACTTGAGGCTAGGAGTTCAGGACCAGCCTGGGCAACATAGTGAGACCTTGTA T C L13304-001,L13705-009 RNACentral:URS000044B5AA,RNACentral:URS00001E2917 scRNA,misc_RNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs541783421 Functional Loss SNV dbSNP153 33..33 33 - - - 3586 RMVar_ID_3586 Human_SNP_ID_470007530 A-to-I Human chr11 - 65375878 65375878 65375878 TTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTCAGCCAGGATGGTCTTGATCTCCTGACTT TTTTGTATTTTTAGTAGAGACAGGGTTTCACCGTGTCAGCCAGGATGGTCTTGATCTCCTGACTT T C SLC25A45 Ensembl:ENSG00000162241 Protein coding exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs190627420 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1258278 3587 RMVar_ID_3587 Human_SNP_ID_470007552 A-to-I Human chr11 - 65375979 65375979 65375979 TGCAACCTCCGCCTTTCCACCTTCCGGGTTCAAGCAACTCTCCTGCCTCAGCCTCCCAAGTAGCT TGCAACCTCCGCCTTTCCACCTTCCGGGTTCAGGCAACTCTCCTGCCTCAGCCTCCCAAGTAGCT T C SLC25A45 Ensembl:ENSG00000162241 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1245674783 Functional Loss SNV dbSNP153 33..33 33 - - - 3588 RMVar_ID_3588 Human_SNP_ID_470015763 A-to-I Human chr11 + 65405502 65405502 65405502 AAAAAGTAGCGAGGTGTATGGCAGGCGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAAA AAAAAGTAGCGAGGTGTATGGCAGGCGCCTGTGATCCCAGCTACTCGGGAGGCTGAGGCAGGAAA A G FRMD8 Ensembl:ENSG00000126391 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1286488014 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101402,RMVar_hsa_circ_115858,RMVar_hsa_circ_150632,RMVar_hsa_circ_110235,RMVar_hsa_circ_150635,RMVar_hsa_circ_150637,RMVar_hsa_circ_119667,RMVar_hsa_circ_150638 3589 RMVar_ID_3589 Human_SNP_ID_470015918 A-to-I Human chr11 + 65406081 65406081 65406081 ACGGAGTCTCACTCTGTCGCCCAGGCTGGAGTACAGTGGCATGATCTCGGCTCACTGCAACCTCC ACGGAGTCTCACTCTGTCGCCCAGGCTGGAGTGCAGTGGCATGATCTCGGCTCACTGCAACCTCC A G FRMD8 Ensembl:ENSG00000126391 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1390057284 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101402,RMVar_hsa_circ_115858,RMVar_hsa_circ_150632,RMVar_hsa_circ_110235,RMVar_hsa_circ_150635,RMVar_hsa_circ_150637,RMVar_hsa_circ_119667,RMVar_hsa_circ_150638 3590 RMVar_ID_3590 Human_SNP_ID_470016066 A-to-I Human chr11 + 65406588 65406588 65406588 CTGTCCTCGTGATCCACCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAAACATCACA CTGTCCTCGTGATCCACCTGCCTTGGCCTCCCGAAGTGCTGGGATTACAGGCGTGAAACATCACA A G FRMD8 Ensembl:ENSG00000126391 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs941859678 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101402,RMVar_hsa_circ_115858,RMVar_hsa_circ_150632,RMVar_hsa_circ_110235,RMVar_hsa_circ_150635,RMVar_hsa_circ_150637,RMVar_hsa_circ_119667,RMVar_hsa_circ_150638 3591 RMVar_ID_3591 Human_SNP_ID_470016067 A-to-I Human chr11 + 65406589 65406589 65406589 TGTCCTCGTGATCCACCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAAACATCACAC TGTCCTCGTGATCCACCTGCCTTGGCCTCCCAGAGTGCTGGGATTACAGGCGTGAAACATCACAC A G FRMD8 Ensembl:ENSG00000126391 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1167836506 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101402,RMVar_hsa_circ_115858,RMVar_hsa_circ_150632,RMVar_hsa_circ_110235,RMVar_hsa_circ_150635,RMVar_hsa_circ_150637,RMVar_hsa_circ_119667,RMVar_hsa_circ_150638 3592 RMVar_ID_3592 Human_SNP_ID_470016328 A-to-I Human chr11 + 65407613 65407613 65407613 CACAAAATAATATTCAGTAAAAAGAAATGGCCAGGCGTGGTGGCTCACGCCTGTAATCCCAGCAC CACAAAATAATATTCAGTAAAAAGAAATGGCCGGGCGTGGTGGCTCACGCCTGTAATCCCAGCAC A G FRMD8 Ensembl:ENSG00000126391 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1457020950 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101402,RMVar_hsa_circ_115858,RMVar_hsa_circ_150632,RMVar_hsa_circ_110235,RMVar_hsa_circ_150635,RMVar_hsa_circ_150637,RMVar_hsa_circ_119667,RMVar_hsa_circ_150638 3593 RMVar_ID_3593 Human_SNP_ID_470016812 A-to-I Human chr11 + 65409321 65409321 65409321 GTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCTGTCCGCCTCAGCCTCCTGAAGTGC GTTGGCCAGGCTGGTCTCGAACTCCTGACCTCGGGTGATCTGTCCGCCTCAGCCTCCTGAAGTGC A G FRMD8 Ensembl:ENSG00000126391 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs981044049 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101402,RMVar_hsa_circ_115858,RMVar_hsa_circ_150632,RMVar_hsa_circ_110235,RMVar_hsa_circ_150635,RMVar_hsa_circ_150637,RMVar_hsa_circ_119667,RMVar_hsa_circ_150638 3594 RMVar_ID_3594 Human_SNP_ID_470016873 A-to-I Human chr11 + 65409590 65409590 65409590 GTCCAGGAGTCCAAGACCAGCCTGCGCAACATAGCAAGACCGCATCTCTATTTAAAAGATTAGCA GTCCAGGAGTCCAAGACCAGCCTGCGCAACATGGCAAGACCGCATCTCTATTTAAAAGATTAGCA A G FRMD8 Ensembl:ENSG00000126391 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1305499123 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101402,RMVar_hsa_circ_115858,RMVar_hsa_circ_150632,RMVar_hsa_circ_110235,RMVar_hsa_circ_150635,RMVar_hsa_circ_150637,RMVar_hsa_circ_119667,RMVar_hsa_circ_150638 3595 RMVar_ID_3595 Human_SNP_ID_470017837 A-to-I Human chr11 + 65413248 65413248 65413248 TGACCTCATGATCTGCCCGCCTCAACCTCCCAAAGTGCTGGGATTATAGGCGTGAGCCACCGCCC TGACCTCATGATCTGCCCGCCTCAACCTCCCACAGTGCTGGGATTATAGGCGTGAGCCACCGCCC A C FRMD8 Ensembl:ENSG00000126391 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1045274593 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101402,RMVar_hsa_circ_115858,RMVar_hsa_circ_150632,RMVar_hsa_circ_110235,RMVar_hsa_circ_150635,RMVar_hsa_circ_150637,RMVar_hsa_circ_119667,RMVar_hsa_circ_150638 3596 RMVar_ID_3596 Human_SNP_ID_470022362 A-to-I Human chr11 - 65429495 65429480 65429496 AAAATCATACACACACACACACACACACACGCACACACACACACACCACAAATGGCCAATTGACA AAAATCATACACACACACACACACACACACG________________ACAAATGGCCAATTGACA TGGTGTGTGTGTGTGTG T L13304-001,L13705-009,TALAM1-001 RNACentral:URS000044B5AA,RNACentral:URS00001E2917,RNACentral:URS00008BCC03 scRNA,misc_RNA,lincRNA intron,intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1175946459 Functional Loss DEL dbSNP153 32..47 33 - - - 3597 RMVar_ID_3597 Human_SNP_ID_470022393 A-to-I Human chr11 - 65429495 65429495 65429495 AAAATCATACACACACACACACACACACACGCACACACACACACACCACAAATGGCCAATTGACA AAAATCATACACACACACACACACACACACGCGCACACACACACACCACAAATGGCCAATTGACA T C L13304-001,L13705-009,TALAM1-001 RNACentral:URS000044B5AA,RNACentral:URS00001E2917,RNACentral:URS00008BCC03 scRNA,misc_RNA,lincRNA intron,intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027165107 Functional Loss SNV dbSNP153 33..33 33 - - - 3598 RMVar_ID_3598 Human_SNP_ID_470044369 A-to-I Human chr11 + 65503818 65503818 65503818 AATGTAACTTTAAGGCAGGAAAGACAAATTTTATTCTTCATAAAGTGATGAGCATATAATAATTC AATGTAACTTTAAGGCAGGAAAGACAAATTTTCTTCTTCATAAAGTGATGAGCATATAATAATTC A C MALAT1 Ensembl:ENSG00000251562 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs145156627 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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 3599 RMVar_ID_3599 Human_SNP_ID_470045274 A-to-I Human chr11 + 65505317 65505317 65505317 AGAAGTGTCAGCCTCACCTGATTTTTATTAGTAATGAGGACTTGCCTCAACTCCCTCTTTCTGGA AGAAGTGTCAGCCTCACCTGATTTTTATTAGTCATGAGGACTTGCCTCAACTCCCTCTTTCTGGA A C MALAT1 Ensembl:ENSG00000251562 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1431373631 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_400823,Human_RBP_ID_868718,Human_RBP_ID_1079323,Human_RBP_ID_1265386,Human_RBP_ID_1781500,Human_RBP_ID_2276112,Human_RBP_ID_3378119,Human_RBP_ID_4171895,Human_RBP_ID_5169395,Human_RBP_ID_5246201,Human_RBP_ID_5549993,Human_RBP_ID_6086238,Human_RBP_ID_8064565,Human_RBP_ID_8355911,Human_RBP_ID_9005475,Human_RBP_ID_9644910,Human_RBP_ID_11674046,Human_RBP_ID_17108745,Human_RBP_ID_17184765,Human_RBP_ID_18176268,Human_RBP_ID_18251636,Human_RBP_ID_18610978,Human_RBP_ID_19583093,Human_RBP_ID_22164920,Human_RBP_ID_22381297,Human_RBP_ID_22791783,Human_RBP_ID_22893117,Human_RBP_ID_23515149,Human_RBP_ID_24404300,Human_RBP_ID_24461873,Human_RBP_ID_24897099,Human_RBP_ID_26410656,Human_RBP_ID_26605402,Human_RBP_ID_26894598,Human_RBP_ID_27205003 RMVar_hsa_circ_150687,RMVar_hsa_circ_150696,RMVar_hsa_circ_150695 3600 RMVar_ID_3600 Human_SNP_ID_470045275 A-to-I Human chr11 + 65505317 65505317 65505317 AGAAGTGTCAGCCTCACCTGATTTTTATTAGTAATGAGGACTTGCCTCAACTCCCTCTTTCTGGA AGAAGTGTCAGCCTCACCTGATTTTTATTAGTGATGAGGACTTGCCTCAACTCCCTCTTTCTGGA A G MALAT1 Ensembl:ENSG00000251562 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1431373631 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_400823,Human_RBP_ID_868718,Human_RBP_ID_1079323,Human_RBP_ID_1265386,Human_RBP_ID_1781500,Human_RBP_ID_2276112,Human_RBP_ID_3378119,Human_RBP_ID_4171895,Human_RBP_ID_5169395,Human_RBP_ID_5246201,Human_RBP_ID_5549993,Human_RBP_ID_6086238,Human_RBP_ID_8064565,Human_RBP_ID_8355911,Human_RBP_ID_9005475,Human_RBP_ID_9644910,Human_RBP_ID_11674046,Human_RBP_ID_17108745,Human_RBP_ID_17184765,Human_RBP_ID_18176268,Human_RBP_ID_18251636,Human_RBP_ID_18610978,Human_RBP_ID_19583093,Human_RBP_ID_22164920,Human_RBP_ID_22381297,Human_RBP_ID_22791783,Human_RBP_ID_22893117,Human_RBP_ID_23515149,Human_RBP_ID_24404300,Human_RBP_ID_24461873,Human_RBP_ID_24897099,Human_RBP_ID_26410656,Human_RBP_ID_26605402,Human_RBP_ID_26894598,Human_RBP_ID_27205003 RMVar_hsa_circ_150687,RMVar_hsa_circ_150696,RMVar_hsa_circ_150695 3601 RMVar_ID_3601 Human_SNP_ID_470059198 A-to-I Human chr11 - 65549517 65549517 65549517 GTGCATGCCTGTAGTCCCAGCTACTCAGGAGAATCACTTGAACCTGGGAGATAGAGGTTGCAGTG GTGCATGCCTGTAGTCCCAGCTACTCAGGAGAGTCACTTGAACCTGGGAGATAGAGGTTGCAGTG T C LTBP3 Ensembl:ENSG00000168056 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs545484063 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94130,RMVar_hsa_circ_150708 3602 RMVar_ID_3602 Human_SNP_ID_470059417 A-to-I Human chr11 - 65550220 65550220 65550220 TATTTTTAGTAGACATGGGGTTTCACCATGTTAATCAGGATGGTCTTGATCTCCTGACCTTGTGA TATTTTTAGTAGACATGGGGTTTCACCATGTTTATCAGGATGGTCTTGATCTCCTGACCTTGTGA T A LTBP3 Ensembl:ENSG00000168056 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490832,GSM3490833,GSM3490834 Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 31158229,32596459 RNA-Seq:(High) rs1034129621 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_109682 RMVar_hsa_circ_94130,RMVar_hsa_circ_150708 3603 RMVar_ID_3603 Human_SNP_ID_470059418 A-to-I Human chr11 - 65550220 65550220 65550220 TATTTTTAGTAGACATGGGGTTTCACCATGTTAATCAGGATGGTCTTGATCTCCTGACCTTGTGA TATTTTTAGTAGACATGGGGTTTCACCATGTTCATCAGGATGGTCTTGATCTCCTGACCTTGTGA T G LTBP3 Ensembl:ENSG00000168056 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490832,GSM3490833,GSM3490834 Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 31158229,32596459 RNA-Seq:(High) rs1034129621 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_109682 RMVar_hsa_circ_94130,RMVar_hsa_circ_150708 3604 RMVar_ID_3604 Human_SNP_ID_470064045 A-to-I Human chr11 - 65567311 65567311 65567311 ATTTTTATTTCTAGTAGAGACGGTGTTTCACCATGTTGGCCAGACTAGTCTCAAGCTCCCGACTT ATTTTTATTTCTAGTAGAGACGGTGTTTCACCTTGTTGGCCAGACTAGTCTCAAGCTCCCGACTT T A L13304-001,L13705-009,lnc-LTBP3-4 RNACentral:URS000044B5AA,RNACentral:URS00001E2917,RNACentral:URS00008BFD37 scRNA,misc_RNA,lincRNA intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1422193212 Functional Loss SNV dbSNP153 33..33 33 - - - 3605 RMVar_ID_3605 Human_SNP_ID_470064144 A-to-I Human chr11 - 65567635 65567635 65567635 ACCACAGCTGGCTAATTTTTTTTTTTTTTTTGAGACGGCATCTTGCTCTGTTGCCCAGGCTGGAG ACCACAGCTGGCTAATTTTTTTTTTTTTTTTGTGACGGCATCTTGCTCTGTTGCCCAGGCTGGAG T A L13304-001,L13705-009,lnc-LTBP3-4 RNACentral:URS000044B5AA,RNACentral:URS00001E2917,RNACentral:URS00008BFD37 scRNA,misc_RNA,lincRNA intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1349697833 Functional Loss SNV dbSNP153 33..33 33 - - - 3606 RMVar_ID_3606 Human_SNP_ID_470064246 A-to-I Human chr11 - 65568092 65568092 65568092 GGCCAGTAGACCAGGTGCTGTGGCTCACACCTATAATCTCAGCACTCTGGGAGGACATGCAGGAG GGCCAGTAGACCAGGTGCTGTGGCTCACACCTGTAATCTCAGCACTCTGGGAGGACATGCAGGAG T C L13304-001,L13705-009,lnc-LTBP3-4 RNACentral:URS000044B5AA,RNACentral:URS00001E2917,RNACentral:URS00008BFD37 scRNA,misc_RNA,lincRNA intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1247600116 Functional Loss SNV dbSNP153 33..33 33 - - - 3607 RMVar_ID_3607 Human_SNP_ID_470091166 A-to-I Human chr11 + 65647971 65647971 65647971 TCGGCTTACTGCAACATCCGCCTCCCAGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCCTTGTAGC TCGGCTTACTGCAACATCCGCCTCCCAGGTTCCAGCAGTTCTCCTGCCTCAGCCTCCCTTGTAGC A C SIPA1 Ensembl:ENSG00000213445 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1475966697 Functional Loss SNV dbSNP153 33..33 33 - - - 3608 RMVar_ID_3608 Human_SNP_ID_470091210 A-to-I Human chr11 + 65648147 65648147 65648147 CACCTGCCTCGCCCTCCCAAAGTTCTGGGATTACAGGCGTGAGTCACCGCGCCCTGAACCTCTAT CACCTGCCTCGCCCTCCCAAAGTTCTGGGATTGCAGGCGTGAGTCACCGCGCCCTGAACCTCTAT A G SIPA1 Ensembl:ENSG00000213445 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs954588693 Functional Loss SNV dbSNP153 33..33 33 - - - 3609 RMVar_ID_3609 Human_SNP_ID_470095310 A-to-I Human chr11 - 65660976 65660976 65660976 GGAGTGCAGTGGCGCGATCTCAGCTCACTGCAACCTCCACCTTCCGGGTTCATGCCATTCTCCTG GGAGTGCAGTGGCGCGATCTCAGCTCACTGCAGCCTCCACCTTCCGGGTTCATGCCATTCTCCTG T C RELA Ensembl:ENSG00000173039 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1243397901 Functional Loss SNV dbSNP153 33..33 33 - - - 3610 RMVar_ID_3610 Human_SNP_ID_470095359 A-to-I Human chr11 - 65661103 65661101 65661103 CTGAGCCCAGGAGGTCACTGCTGCGGCAAGCTATGATTGCACCACTGCACTTGGGTGGCAGGGCG CTGAGCCCAGGAGGTCACTGCTGCGGCAAGCT__GATTGCACCACTGCACTTGGGTGGCAGGGCG CAT C RELA Ensembl:ENSG00000173039 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs928657185 Functional Loss DEL dbSNP153 33..34 33 - - - 3611 RMVar_ID_3611 Human_SNP_ID_470095369 A-to-I Human chr11 - 65661127 65661127 65661127 GGGAGGCTGAGGTGGGAGGATCGCCTGAGCCCAGGAGGTCACTGCTGCGGCAAGCTATGATTGCA GGGAGGCTGAGGTGGGAGGATCGCCTGAGCCCTGGAGGTCACTGCTGCGGCAAGCTATGATTGCA T A RELA Ensembl:ENSG00000173039 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs993264133 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17560005 3612 RMVar_ID_3612 Human_SNP_ID_470095388 A-to-I Human chr11 - 65661195 65661195 65661195 TAGTGAGACCCCATGTCTACAAAAAATAAGAAATTAGCTGGGTATGGTGGCATGCGCCTATAGTC TAGTGAGACCCCATGTCTACAAAAAATAAGAAGTTAGCTGGGTATGGTGGCATGCGCCTATAGTC T C RELA Ensembl:ENSG00000173039 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1321352255 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17560005 3613 RMVar_ID_3613 Human_SNP_ID_470095390 A-to-I Human chr11 - 65661199 65661199 65661199 AACATAGTGAGACCCCATGTCTACAAAAAATAAGAAATTAGCTGGGTATGGTGGCATGCGCCTAT AACATAGTGAGACCCCATGTCTACAAAAAATAGGAAATTAGCTGGGTATGGTGGCATGCGCCTAT T C RELA Ensembl:ENSG00000173039 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1375883328 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17560005 3614 RMVar_ID_3614 Human_SNP_ID_470118606 A-to-I Human chr11 - 65752005 65752005 65752005 GGGAGGCTGAGATGGGAGAATTGCTTGAGCCCAGGAGGCTGAGGATTCAGTGAGCTATGATCACA GGGAGGCTGAGATGGGAGAATTGCTTGAGCCCGGGAGGCTGAGGATTCAGTGAGCTATGATCACA T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs891074076 Functional Loss SNV dbSNP153 33..33 33 - - - 3615 RMVar_ID_3615 Human_SNP_ID_470122548 A-to-I Human chr11 - 65767459 65767459 65767459 AAAATCAGCTGGATGTGGTAGCTCATGCCTATAGTCCTTAACATTTTGGGAGGCTAAGGCAGGAG AAAATCAGCTGGATGTGGTAGCTCATGCCTATGGTCCTTAACATTTTGGGAGGCTAAGGCAGGAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs528129105 Functional Loss SNV dbSNP153 33..33 33 - - - 3616 RMVar_ID_3616 Human_SNP_ID_470122549 A-to-I Human chr11 - 65767461 65767461 65767461 ACAAAATCAGCTGGATGTGGTAGCTCATGCCTATAGTCCTTAACATTTTGGGAGGCTAAGGCAGG ACAAAATCAGCTGGATGTGGTAGCTCATGCCTGTAGTCCTTAACATTTTGGGAGGCTAAGGCAGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202589735 Functional Loss SNV dbSNP153 33..33 33 - - - 3617 RMVar_ID_3617 Human_SNP_ID_470123823 A-to-I Human chr11 - 65772830 65772829 65772831 TTGTCCAGGCTGGTTAAGGCCTCCTGGGTTCAAGTGATCCTCCTGCCTTGGCCTCCCAAAGTGCT TTGTCCAGGCTGGTTAAGGCCTCCTGGGTTC__GTGATCCTCCTGCCTTGGCCTCCCAAAGTGCT CTT C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1435136981 Functional Loss DEL dbSNP153 32..33 33 - - - 3618 RMVar_ID_3618 Human_SNP_ID_470123860 A-to-I Human chr11 - 65772989 65772989 65772989 GCTGGAGTGCAGTGGTGCGATCATAGCTCACTACAACCTCAAACTCCTGGGCAAAAGTGATCCTC GCTGGAGTGCAGTGGTGCGATCATAGCTCACTGCAACCTCAAACTCCTGGGCAAAAGTGATCCTC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs951220955 Functional Loss SNV dbSNP153 33..33 33 - - - 3619 RMVar_ID_3619 Human_SNP_ID_470124222 A-to-I Human chr11 - 65774483 65774483 65774483 CGCTTGAACCCGGGAGGTGGAGGTTGCAGTGAACTGAGATTGGGCCACTACACTCCAGCCTGGAT CGCTTGAACCCGGGAGGTGGAGGTTGCAGTGAGCTGAGATTGGGCCACTACACTCCAGCCTGGAT T C AP5B1 Ensembl:ENSG00000254470 Protein coding 3'UTR GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1481389953 Functional Loss SNV dbSNP153 33..33 33 - - - 3620 RMVar_ID_3620 Human_SNP_ID_470124229 A-to-I Human chr11 - 65774508 65774508 65774508 ACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGGGAGGTGGAGGTTGCAGTGAACTGAGAT ACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAGCCCGGGAGGTGGAGGTTGCAGTGAACTGAGAT T C AP5B1 Ensembl:ENSG00000254470 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1007903005 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27414585 3621 RMVar_ID_3621 Human_SNP_ID_470124601 A-to-I Human chr11 - 65776002 65775999 65776003 CCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATTACTTGAACCTGGGAGGCAGAAGTT CCTGTAATCCCAGCTACTTGGGAGGCTGAGG____AGAATTACTTGAACCTGGGAGGCAGAAGTT TCCTG T AP5B1 Ensembl:ENSG00000254470 Protein coding 3'UTR GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1178696852 Functional Loss DEL dbSNP153 32..35 33 - - - 3622 RMVar_ID_3622 Human_SNP_ID_470124639 A-to-I Human chr11 - 65776163 65776163 65776163 GCCTGGGCTGGGTGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGAGAGGCTGCGGCGGGTGGA GCCTGGGCTGGGTGCGGTGGCTCATGCCTGTAGTCCCAGCACTTTGAGAGGCTGCGGCGGGTGGA T C AP5B1 Ensembl:ENSG00000254470 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 31158229,32596459,32596459 RNA-Seq:(High) rs1322830423 Functional Loss SNV dbSNP153 33..33 33 - - - 3623 RMVar_ID_3623 Human_SNP_ID_470124833 A-to-I Human chr11 - 65776910 65776910 65776910 TTCCTAGGCTGGTCTCGAACTCCTGGGCTTAAATGACTCTTCTGCCTCAGCCTCACCAAAGTGTT TTCCTAGGCTGGTCTCGAACTCCTGGGCTTAAGTGACTCTTCTGCCTCAGCCTCACCAAAGTGTT T C AP5B1 Ensembl:ENSG00000254470 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 31158229,32596459,32596459 RNA-Seq:(High) rs991375496 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_401042,Human_RBP_ID_11675197,Human_RBP_ID_26409714 3624 RMVar_ID_3624 Human_SNP_ID_470124840 A-to-I Human chr11 - 65776937 65776937 65776937 TATTTTTTGCAGACAGGATCTCCCTGTTTCCTAGGCTGGTCTCGAACTCCTGGGCTTAAATGACT TATTTTTTGCAGACAGGATCTCCCTGTTTCCTGGGCTGGTCTCGAACTCCTGGGCTTAAATGACT T C AP5B1 Ensembl:ENSG00000254470 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs377001935 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_401042,Human_RBP_ID_11675197,Human_RBP_ID_26408710 3625 RMVar_ID_3625 Human_SNP_ID_470124853 A-to-I Human chr11 - 65776989 65776989 65776989 CCATCTCAGCCTGCCTCCGAGTAGCTGGGACTACAGGTGTGAGTCACCACTGTATTTTTTGCAGA CCATCTCAGCCTGCCTCCGAGTAGCTGGGACTGCAGGTGTGAGTCACCACTGTATTTTTTGCAGA T C AP5B1 Ensembl:ENSG00000254470 Protein coding 3'UTR GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs764786107 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17799342,Human_RBP_ID_26408710 3626 RMVar_ID_3626 Human_SNP_ID_470124866 A-to-I Human chr11 - 65777032 65777032 65777032 AGGGATCATTGCAGACTCTGCCTCTCAGGCTCAGGTGATCCTCCCATCTCAGCCTGCCTCCGAGT AGGGATCATTGCAGACTCTGCCTCTCAGGCTCGGGTGATCCTCCCATCTCAGCCTGCCTCCGAGT T C AP5B1 Ensembl:ENSG00000254470 Protein coding 3'UTR GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831 HepG2 cell line;ASD brains,frontal_cortex;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line - 29129909,30559470,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs1356423579 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26409716 3627 RMVar_ID_3627 Human_SNP_ID_470124867 A-to-I Human chr11 - 65777038 65777038 65777038 GTGATTAGGGATCATTGCAGACTCTGCCTCTCAGGCTCAGGTGATCCTCCCATCTCAGCCTGCCT GTGATTAGGGATCATTGCAGACTCTGCCTCTCCGGCTCAGGTGATCCTCCCATCTCAGCCTGCCT T G AP5B1 Ensembl:ENSG00000254470 Protein coding 3'UTR GSE100210;GSE107867;GSE107867 HepG2 cell line;ASD brains,frontal_cortex;ASD brains,temporal_cortex - 29129909,30559470,30559470 RNA-Seq:(High) rs1315195925 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26409716 3628 RMVar_ID_3628 Human_SNP_ID_470124881 A-to-I Human chr11 - 65777096 65777092 65777096 TTTTTTCGGGGAGGGGTTAAAGACAGGATCTCACTCTGGCGCTCTGGAGTGCAGTGGTGTGATTA TTTTTTCGGGGAGGGGTTAAAGACAGGATCTC____TGGCGCTCTGGAGTGCAGTGGTGTGATTA AGAGT A AP5B1 Ensembl:ENSG00000254470 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs1179833292 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_401043,Human_RBP_ID_11675203,Human_RBP_ID_26894911 3629 RMVar_ID_3629 Human_SNP_ID_470142071 A-to-I Human chr11 + 65839682 65839682 65839682 ATAAGTAACTAAAAAAATTTTTTTTGTGAACCATGATCACACCACTGCACTCTAGCCTGGGTGAC ATAAGTAACTAAAAAAATTTTTTTTGTGAACCGTGATCACACCACTGCACTCTAGCCTGGGTGAC A G SNX32 Ensembl:ENSG00000172803 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs962417570 Functional Loss SNV dbSNP153 33..33 33 - - - 3630 RMVar_ID_3630 Human_SNP_ID_470160694 A-to-I Human chr11 - 65898205 65898205 65898205 GAAACCCTGTCTCTACTAAAAATACAAAAATTAGCCGGGCACAGTTGTGGGCGCCTGTAGTCCCA GAAACCCTGTCTCTACTAAAAATACAAAAATTTGCCGGGCACAGTTGTGGGCGCCTGTAGTCCCA T A FOSL1 Ensembl:ENSG00000175592 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1421105424 Functional Loss SNV dbSNP153 33..33 33 - - - 3631 RMVar_ID_3631 Human_SNP_ID_470180244 A-to-I Human chr11 + 65968184 65968184 65968184 GTTGGCCAGGCTGGTCTCCAACTCCTGACCTCATGATCTGCCTGCCTCTGCCTCCGAAAATGCTA GTTGGCCAGGCTGGTCTCCAACTCCTGACCTCGTGATCTGCCTGCCTCTGCCTCCGAAAATGCTA A G SART1 Ensembl:ENSG00000175467 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1443695632 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22893236 RMVar_hsa_circ_71217 3632 RMVar_ID_3632 Human_SNP_ID_470180723 A-to-I Human chr11 + 65970002 65970002 65970002 CCTCAGCCTCCCAAAGTGCTGGAATTAGAGGCATGAACCACCACACCCGGCCACCTAGAAGGTTT CCTCAGCCTCCCAAAGTGCTGGAATTAGAGGCGTGAACCACCACACCCGGCCACCTAGAAGGTTT A G SART1 Ensembl:ENSG00000175467 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1422472365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11675787 RMVar_hsa_circ_71217 3633 RMVar_ID_3633 Human_SNP_ID_470181593 A-to-I Human chr11 + 65973059 65973059 65973059 AACCAGACGTGGTGGCGGGCACCTGTAGTCCCAGCTACTAGGGAGGCTGAGGCAGGAGAATGGTG AACCAGACGTGGTGGCGGGCACCTGTAGTCCCTGCTACTAGGGAGGCTGAGGCAGGAGAATGGTG A T SART1 Ensembl:ENSG00000175467 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1228717611 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_111869 RMVar_hsa_circ_71217 3634 RMVar_ID_3634 Human_SNP_ID_470182665 A-to-I Human chr11 + 65976555 65976555 65976555 CACCTACGGGCTGGCTGGCAATCGCGAGGAGCAGGAGGAGCTCATGGTGCGTCTGGGGCGGCCCC CACCTACGGGCTGGCTGGCAATCGCGAGGAGCGGGAGGAGCTCATGGTGCGTCTGGGGCGGCCCC A G SART1 Ensembl:ENSG00000175467 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1439053488 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8774375,Human_RBP_ID_18410508,Human_RBP_ID_19049928 Human_Splice_Rec_1261297 RMVar_hsa_circ_71217,RMVar_hsa_circ_377971 3635 RMVar_ID_3635 Human_SNP_ID_470210612 A-to-I Human chr11 + 66077305 66077305 66077305 CATTCCAAGGCTGGGCGTGGTGGCTCATGCCTATCATCCCAGCACTTTGGGAGGCTGAGGCGGAA CATTCCAAGGCTGGGCGTGGTGGCTCATGCCTGTCATCCCAGCACTTTGGGAGGCTGAGGCGGAA A G PACS1 Ensembl:ENSG00000175115 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs558643036 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101287,RMVar_hsa_circ_150828 3636 RMVar_ID_3636 Human_SNP_ID_470210767 A-to-I Human chr11 + 66077862 66077862 66077862 GTAGCTGGGATTCCAGGCATGCACCACCATGCATGGATAATTTTGTATTTTTAGTAGAGACGGGG GTAGCTGGGATTCCAGGCATGCACCACCATGCGTGGATAATTTTGTATTTTTAGTAGAGACGGGG A G PACS1 Ensembl:ENSG00000175115 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs569982688 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101287,RMVar_hsa_circ_150828 3637 RMVar_ID_3637 Human_SNP_ID_470210768 A-to-I Human chr11 + 66077862 66077862 66077862 GTAGCTGGGATTCCAGGCATGCACCACCATGCATGGATAATTTTGTATTTTTAGTAGAGACGGGG GTAGCTGGGATTCCAGGCATGCACCACCATGCTTGGATAATTTTGTATTTTTAGTAGAGACGGGG A T PACS1 Ensembl:ENSG00000175115 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs569982688 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101287,RMVar_hsa_circ_150828 3638 RMVar_ID_3638 Human_SNP_ID_470211810 A-to-I Human chr11 + 66082324 66082324 66082324 ATAGCTCACTGCAGCCTCGAATTCCTGGACTCAAGTGATCCTCTAACCTCAGTCTTCCAAGTAAA ATAGCTCACTGCAGCCTCGAATTCCTGGACTCGAGTGATCCTCTAACCTCAGTCTTCCAAGTAAA A G PACS1 Ensembl:ENSG00000175115 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1411946927 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11677010 RMVar_hsa_circ_101287,RMVar_hsa_circ_150828 3639 RMVar_ID_3639 Human_SNP_ID_470213445 A-to-I Human chr11 + 66089765 66089765 66089765 GCGATGGCTCACGTCTGTAATTCCAGCACTTTAGGATGCCAAGGTGGGCAGATCACAAGGTCAGG GCGATGGCTCACGTCTGTAATTCCAGCACTTTCGGATGCCAAGGTGGGCAGATCACAAGGTCAGG A C PACS1 Ensembl:ENSG00000175115 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1344141705 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101287,RMVar_hsa_circ_150828 3640 RMVar_ID_3640 Human_SNP_ID_470213625 A-to-I Human chr11 + 66090334 66090334 66090334 TTGCTCTGTTGCCCATGCTGGAGCACAGTGGCATGATCTCAGCTCACTGCAGCCTGAACCTCCCA TTGCTCTGTTGCCCATGCTGGAGCACAGTGGCGTGATCTCAGCTCACTGCAGCCTGAACCTCCCA A G PACS1 Ensembl:ENSG00000175115 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs940017401 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17560006 RMVar_hsa_circ_101287,RMVar_hsa_circ_150828 3641 RMVar_ID_3641 Human_SNP_ID_470213807 A-to-I Human chr11 + 66091200 66091200 66091200 GACTCTCACTCCAGCCCAGGCTGGAGTGCAGTAGTGGATCTCAGATCACTGCAACCTCCGCCTCC GACTCTCACTCCAGCCCAGGCTGGAGTGCAGTGGTGGATCTCAGATCACTGCAACCTCCGCCTCC A G PACS1 Ensembl:ENSG00000175115 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1392921408 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_750495,Human_RBP_ID_11677332 RMVar_hsa_circ_101287,RMVar_hsa_circ_150828 3642 RMVar_ID_3642 Human_SNP_ID_470213809 A-to-I Human chr11 + 66091210 66091210 66091210 CCAGCCCAGGCTGGAGTGCAGTAGTGGATCTCAGATCACTGCAACCTCCGCCTCCCAAGTTAAAG CCAGCCCAGGCTGGAGTGCAGTAGTGGATCTCGGATCACTGCAACCTCCGCCTCCCAAGTTAAAG A G PACS1 Ensembl:ENSG00000175115 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs558706256 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_750495,Human_RBP_ID_11677332 RMVar_hsa_circ_101287,RMVar_hsa_circ_150828 3643 RMVar_ID_3643 Human_SNP_ID_470223220 A-to-I Human chr11 + 66132717 66132717 66132717 TTGAGATGGAGTTTTACTCTCTTGCCCAGGCTAGAGTGCAGTGGTGGGATCTCTGCTCACTGCAA TTGAGATGGAGTTTTACTCTCTTGCCCAGGCTTGAGTGCAGTGGTGGGATCTCTGCTCACTGCAA A T PACS1 Ensembl:ENSG00000175115 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs895340809 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101287,RMVar_hsa_circ_150828 3644 RMVar_ID_3644 Human_SNP_ID_470227159 A-to-I Human chr11 + 66149954 66149954 66149954 TATTTTTAGTAGAGATGGGGTTTCTCCATGTTAGTCAGGCTGGTCTCGAACTTGCCACCTCAGGC TATTTTTAGTAGAGATGGGGTTTCTCCATGTTCGTCAGGCTGGTCTCGAACTTGCCACCTCAGGC A C PACS1 Ensembl:ENSG00000175115 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1026837019 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101287,RMVar_hsa_circ_150828 3645 RMVar_ID_3645 Human_SNP_ID_470229015 A-to-I Human chr11 + 66158203 66158203 66158203 GTTGCCCAGACTAGTCTCGAGCTCCTGAGCTCAAGTGATCCACTGGCTTTGGCTTCCCAAAGTGC GTTGCCCAGACTAGTCTCGAGCTCCTGAGCTCGAGTGATCCACTGGCTTTGGCTTCCCAAAGTGC A G PACS1 Ensembl:ENSG00000175115 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1412203732 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101287,RMVar_hsa_circ_150828 3646 RMVar_ID_3646 Human_SNP_ID_470237165 A-to-I Human chr11 + 66194951 66194951 66194951 TAGTTCTCAAAACTTAAAATGTTGGGCCGGGCACTGTGGCTCACACCTGTAATCCCAGCACTTTG TAGTTCTCAAAACTTAAAATGTTGGGCCGGGCGCTGTGGCTCACACCTGTAATCCCAGCACTTTG A G PACS1 Ensembl:ENSG00000175115 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1402933982 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35747,RMVar_hsa_circ_296271,RMVar_hsa_circ_101287,RMVar_hsa_circ_150828,RMVar_hsa_circ_366116,RMVar_hsa_circ_83761,RMVar_hsa_circ_92488,RMVar_hsa_circ_77681,RMVar_hsa_circ_150830,RMVar_hsa_circ_150831,RMVar_hsa_circ_150832,RMVar_hsa_circ_150829 3647 RMVar_ID_3647 Human_SNP_ID_470237166 A-to-I Human chr11 + 66194951 66194951 66194951 TAGTTCTCAAAACTTAAAATGTTGGGCCGGGCACTGTGGCTCACACCTGTAATCCCAGCACTTTG TAGTTCTCAAAACTTAAAATGTTGGGCCGGGCTCTGTGGCTCACACCTGTAATCCCAGCACTTTG A T PACS1 Ensembl:ENSG00000175115 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1402933982 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35747,RMVar_hsa_circ_296271,RMVar_hsa_circ_101287,RMVar_hsa_circ_150828,RMVar_hsa_circ_366116,RMVar_hsa_circ_83761,RMVar_hsa_circ_92488,RMVar_hsa_circ_77681,RMVar_hsa_circ_150830,RMVar_hsa_circ_150831,RMVar_hsa_circ_150832,RMVar_hsa_circ_150829 3648 RMVar_ID_3648 Human_SNP_ID_470241571 A-to-I Human chr11 + 66213126 66213126 66213126 CCGCTGCTTTGGCCTCCCAGAGTGCTGGGATTACAGGCGTGAGCCACTGCTCCCGGCCTCATTAA CCGCTGCTTTGGCCTCCCAGAGTGCTGGGATTCCAGGCGTGAGCCACTGCTCCCGGCCTCATTAA A C PACS1 Ensembl:ENSG00000175115 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1034557401 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35747,RMVar_hsa_circ_101287,RMVar_hsa_circ_150828,RMVar_hsa_circ_366116,RMVar_hsa_circ_83761,RMVar_hsa_circ_77681,RMVar_hsa_circ_338196,RMVar_hsa_circ_150831,RMVar_hsa_circ_150832,RMVar_hsa_circ_349192,RMVar_hsa_circ_150834 3649 RMVar_ID_3649 Human_SNP_ID_470253381 A-to-I Human chr11 + 66260938 66260938 66260938 TAAATTAGCCAGCTGTGGTGGTGTGCACCCGTAGTCCCAGTTACTCAGGAGGCTGAGGGGGAAGG TAAATTAGCCAGCTGTGGTGGTGTGCACCCGTGGTCCCAGTTACTCAGGAGGCTGAGGGGGAAGG A G KLC2 Ensembl:ENSG00000174996 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1364433071 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17560007 RMVar_hsa_circ_150858,RMVar_hsa_circ_362982 3650 RMVar_ID_3650 Human_SNP_ID_470256610 A-to-I Human chr11 + 66270498 66270498 66270498 CACTCTGGAGGGTGAGACAGGAGAATCACTTGAACCAGGGAGTCGGACGTTGCAGTGAGCCGAGA CACTCTGGAGGGTGAGACAGGAGAATCACTTGTACCAGGGAGTCGGACGTTGCAGTGAGCCGAGA A T RAB1B Ensembl:ENSG00000174903 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1390763785 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114115,RMVar_hsa_circ_150860 3651 RMVar_ID_3651 Human_SNP_ID_470283988 A-to-I Human chr11 + 66364669 66364669 66364669 TGGGACTATAGGCGCCTGCCACCACCATGCCCAGATAATTTTTATATTTTTAGTAGAGCCAGGTT TGGGACTATAGGCGCCTGCCACCACCATGCCCGGATAATTTTTATATTTTTAGTAGAGCCAGGTT A G AP001107.9 Ensembl:ENSG00000255468 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1214677681 Functional Loss SNV dbSNP153 33..33 33 - - - 3652 RMVar_ID_3652 Human_SNP_ID_470319093 A-to-I Human chr11 + 66502671 66502671 66502671 TTTTTAGTAGAGATGGGGTTTCACCCCATGTTAGCCAGGATGGTCTCGATCTCCTGACCTCGTGA TTTTTAGTAGAGATGGGGTTTCACCCCATGTTGGCCAGGATGGTCTCGATCTCCTGACCTCGTGA A G DPP3 Ensembl:ENSG00000254986 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1365364639 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109976,RMVar_hsa_circ_150893 3653 RMVar_ID_3653 Human_SNP_ID_470319468 A-to-I Human chr11 + 66504291 66504291 66504291 TTTTTTTTTCCATAGAGATATGGTCTTGCCATATTGTCCAGGCTGGTCTCAAACTCCTGGGCTCA TTTTTTTTTCCATAGAGATATGGTCTTGCCATGTTGTCCAGGCTGGTCTCAAACTCCTGGGCTCA A G DPP3 Ensembl:ENSG00000254986 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs995097036 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109976,RMVar_hsa_circ_150893 3654 RMVar_ID_3654 Human_SNP_ID_470322888 A-to-I Human chr11 + 66517060 66517060 66517060 TCTCTACTAAAAATACAAAAAATTAGCCGGGCATGGTAGCGGTCGCCTGTACTCCCAGCTACTCA TCTCTACTAAAAATACAAAAAATTAGCCGGGCGTGGTAGCGGTCGCCTGTACTCCCAGCTACTCA A G AP002748.5,BBS1 Ensembl:ENSG00000256349,Ensembl:ENSG00000174483 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs957182110 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150900,RMVar_hsa_circ_378896,RMVar_hsa_circ_97311,RMVar_hsa_circ_150899 3655 RMVar_ID_3655 Human_SNP_ID_470322889 A-to-I Human chr11 + 66517065 66517065 66517065 ACTAAAAATACAAAAAATTAGCCGGGCATGGTAGCGGTCGCCTGTACTCCCAGCTACTCAGGAGG ACTAAAAATACAAAAAATTAGCCGGGCATGGTGGCGGTCGCCTGTACTCCCAGCTACTCAGGAGG A G AP002748.5,BBS1 Ensembl:ENSG00000256349,Ensembl:ENSG00000174483 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1369670406 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150900,RMVar_hsa_circ_378896,RMVar_hsa_circ_97311,RMVar_hsa_circ_150899 3656 RMVar_ID_3656 Human_SNP_ID_470323215 A-to-I Human chr11 + 66518185 66518185 66518185 CTCCCTGTTGGTCAGGCTGGTCTCGAACTCCCAACCTCACGTGATCCACCCACCTCGGCCTCCCA CTCCCTGTTGGTCAGGCTGGTCTCGAACTCCCGACCTCACGTGATCCACCCACCTCGGCCTCCCA A G AP002748.5,BBS1 Ensembl:ENSG00000256349,Ensembl:ENSG00000174483 Protein coding,Protein coding intron,intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1026484446 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11680020 RMVar_hsa_circ_150900,RMVar_hsa_circ_378896,RMVar_hsa_circ_97311,RMVar_hsa_circ_150899 3657 RMVar_ID_3657 Human_SNP_ID_470323410 A-to-I Human chr11 + 66518960 66518960 66518960 TTTATTTTTATTTTTTGTAGAGTTGGGGTCTCACTTTGCTGCCCAAGCTGGTCTTGGACTCCTGG TTTATTTTTATTTTTTGTAGAGTTGGGGTCTCGCTTTGCTGCCCAAGCTGGTCTTGGACTCCTGG A G AP002748.5,BBS1 Ensembl:ENSG00000256349,Ensembl:ENSG00000174483 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs920624366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227103,Human_RBP_ID_11680054 RMVar_hsa_circ_150900,RMVar_hsa_circ_378896,RMVar_hsa_circ_97311,RMVar_hsa_circ_150899 3658 RMVar_ID_3658 Human_SNP_ID_470347070 A-to-I Human chr11 + 66601646 66601646 66601646 GCTGGAGTGCAGTGCTGTGATCATGGCTCACTACAGCCTTGAACTCATGGGCTCAAGCAATCCTC GCTGGAGTGCAGTGCTGTGATCATGGCTCACTGCAGCCTTGAACTCATGGGCTCAAGCAATCCTC A G CCS Ensembl:ENSG00000173992 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs767212045 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11680400 RMVar_hsa_circ_8594,RMVar_hsa_circ_83359,RMVar_hsa_circ_120622,RMVar_hsa_circ_150912,RMVar_hsa_circ_114886,RMVar_hsa_circ_77382,RMVar_hsa_circ_150913,RMVar_hsa_circ_150914,RMVar_hsa_circ_150916 3659 RMVar_ID_3659 Human_SNP_ID_470347586 A-to-I Human chr11 + 66603923 66603923 66603923 GGTGGCGTGCTCTGTAGTCACAGCTACTCGGGAAGCTGAGACAGGAGAATTGCTTGAACCTGGGG GGTGGCGTGCTCTGTAGTCACAGCTACTCGGGTAGCTGAGACAGGAGAATTGCTTGAACCTGGGG A T CCS Ensembl:ENSG00000173992 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs531544437 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8594,RMVar_hsa_circ_83359,RMVar_hsa_circ_120622,RMVar_hsa_circ_150912,RMVar_hsa_circ_114886,RMVar_hsa_circ_77382,RMVar_hsa_circ_150913,RMVar_hsa_circ_150914,RMVar_hsa_circ_150916 3660 RMVar_ID_3660 Human_SNP_ID_470349118 A-to-I Human chr11 + 66609568 66609568 66609568 GCCACCACGCCCGGCTAATTTTTTGTATTTTTAGTAGAGATGGGTTTTCATCATGTTAGCCAGTT GCCACCACGCCCGGCTAATTTTTTGTATTTTTCGTAGAGATGGGTTTTCATCATGTTAGCCAGTT A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1262885484 Functional Loss SNV dbSNP153 33..33 33 - - - 3661 RMVar_ID_3661 Human_SNP_ID_470350801 A-to-I Human chr11 + 66615850 66615850 66615850 GACCTCCGGTGATCTGCTTGCCTTGGTCTCCCAAAGTGCTGGAATTACAGGCGTGAGCCACCGCT GACCTCCGGTGATCTGCTTGCCTTGGTCTCCCCAAGTGCTGGAATTACAGGCGTGAGCCACCGCT A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1029738842 Functional Loss SNV dbSNP153 33..33 33 - - - 3662 RMVar_ID_3662 Human_SNP_ID_470354967 A-to-I Human chr11 + 66629814 66629814 66629814 TGCTTCAAATGTGGCCAGGTGTGGTAGCTCACACCTGTAATTCCCAGCGCTTTGGGAATTTGAGG TGCTTCAAATGTGGCCAGGTGTGGTAGCTCACGCCTGTAATTCCCAGCGCTTTGGGAATTTGAGG A G RBM14,RBM14-RBM4 Ensembl:ENSG00000239306,Ensembl:ENSG00000248643 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1412969817 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117738,RMVar_hsa_circ_150921 3663 RMVar_ID_3663 Human_SNP_ID_470355121 A-to-I Human chr11 + 66630325 66630325 66630325 GACTTGGGGCAGGTGTCATGGCTCACGTTTGTAATCCTAGCACTTTGGGAGGCCGGGGTGGTTGG GACTTGGGGCAGGTGTCATGGCTCACGTTTGTGATCCTAGCACTTTGGGAGGCCGGGGTGGTTGG A G RBM14-RBM4 Ensembl:ENSG00000248643 Protein coding intron GSE38233;GSE107867 cultured B-cells;ASD brains,cerebellum - 24183664,30559470 RNA-Seq:(High) rs1489624049 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11681454,Human_RBP_ID_17799754 RMVar_hsa_circ_117738,RMVar_hsa_circ_150921 3664 RMVar_ID_3664 Human_SNP_ID_470355137 A-to-I Human chr11 + 66630372 66630372 66630372 GGAGGCCGGGGTGGTTGGATCCTTTTGAGTCCAGGAGTTCAAGACCAGCCTGGGCTACATGGGTA GGAGGCCGGGGTGGTTGGATCCTTTTGAGTCCGGGAGTTCAAGACCAGCCTGGGCTACATGGGTA A G RBM14-RBM4 Ensembl:ENSG00000248643 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1393896617 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11681455 RMVar_hsa_circ_117738,RMVar_hsa_circ_150921 3665 RMVar_ID_3665 Human_SNP_ID_470355146 A-to-I Human chr11 + 66630419 66630419 66630419 GCCTGGGCTACATGGGTAAACTTCATCTGTACAAAAAATAAAAAACTAGCCAGCCGTGGTGGTAC GCCTGGGCTACATGGGTAAACTTCATCTGTACCAAAAATAAAAAACTAGCCAGCCGTGGTGGTAC A C RBM14-RBM4 Ensembl:ENSG00000248643 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1168512338 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17560377,Human_RBP_ID_17799755 RMVar_hsa_circ_117738,RMVar_hsa_circ_150921 3666 RMVar_ID_3666 Human_SNP_ID_470355249 A-to-I Human chr11 + 66630722 66630722 66630722 TGTTGCCTAGGCTACACTTGAACACGTGGCTCAAGTGATCTTCCTACCTCAGGCTCCCAAGTAGC TGTTGCCTAGGCTACACTTGAACACGTGGCTCGAGTGATCTTCCTACCTCAGGCTCCCAAGTAGC A G RBM14-RBM4 Ensembl:ENSG00000248643 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956493973 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6087567,Human_RBP_ID_11681470 RMVar_hsa_circ_117738,RMVar_hsa_circ_150921 3667 RMVar_ID_3667 Human_SNP_ID_470355254 A-to-I Human chr11 + 66630735 66630735 66630735 ACACTTGAACACGTGGCTCAAGTGATCTTCCTACCTCAGGCTCCCAAGTAGCTGGGACTACAGGA ACACTTGAACACGTGGCTCAAGTGATCTTCCTGCCTCAGGCTCCCAAGTAGCTGGGACTACAGGA A G RBM14-RBM4 Ensembl:ENSG00000248643 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1166883094 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6087567,Human_RBP_ID_11681470 RMVar_hsa_circ_117738,RMVar_hsa_circ_150921 3668 RMVar_ID_3668 Human_SNP_ID_470355495 A-to-I Human chr11 + 66631547 66631545 66631547 TGACCTCGTGATCTGCCCGCCTTGGCCTCCCAAAGTGCTTGGATTACAGGCGTGAGCCACTACGC TGACCTCGTGATCTGCCCGCCTTGGCCTCCC__AGTGCTTGGATTACAGGCGTGAGCCACTACGC CAA C RBM14-RBM4 Ensembl:ENSG00000248643 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978110868 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_117738,RMVar_hsa_circ_150921 3669 RMVar_ID_3669 Human_SNP_ID_470355574 A-to-I Human chr11 + 66631818 66631818 66631818 CACTACACCCAGCTAATTTTTCTATTTTTAGTAGAGATGGGGTTTTACCATATTGGCCAGGCTGG CACTACACCCAGCTAATTTTTCTATTTTTAGTGGAGATGGGGTTTTACCATATTGGCCAGGCTGG A G RBM14-RBM4 Ensembl:ENSG00000248643 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs913547221 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117738,RMVar_hsa_circ_150921 3670 RMVar_ID_3670 Human_SNP_ID_470355582 A-to-I Human chr11 + 66631837 66631837 66631837 TTCTATTTTTAGTAGAGATGGGGTTTTACCATATTGGCCAGGCTGGTCTCGAACTCCTGACCTCA TTCTATTTTTAGTAGAGATGGGGTTTTACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCA A G RBM14-RBM4 Ensembl:ENSG00000248643 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1167697919 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117738,RMVar_hsa_circ_150921 3671 RMVar_ID_3671 Human_SNP_ID_470355824 A-to-I Human chr11 + 66632801 66632801 66632801 TGTAATCCCAGCTACTCGGGAGGCTGAGGCATAAGAATCGCTTGAACCTGGGAGGCAGAGGTTGC TGTAATCCCAGCTACTCGGGAGGCTGAGGCATGAGAATCGCTTGAACCTGGGAGGCAGAGGTTGC A G RBM14-RBM4 Ensembl:ENSG00000248643 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1275561904 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23305178 RMVar_hsa_circ_117738,RMVar_hsa_circ_150921 3672 RMVar_ID_3672 Human_SNP_ID_470355963 A-to-I Human chr11 + 66633317 66633317 66633317 TTGGCTCACTGCAGCCTCTGCCTCCTGAGCTCAGGTGATTCTCCCACCTCAGCCTCCCAAGTGGC TTGGCTCACTGCAGCCTCTGCCTCCTGAGCTCGGGTGATTCTCCCACCTCAGCCTCCCAAGTGGC A G RBM14-RBM4 Ensembl:ENSG00000248643 Protein coding intron GSE107867 ASD brains,frontal_cortex;ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1443985044 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117738,RMVar_hsa_circ_150921 3673 RMVar_ID_3673 Human_SNP_ID_470355964 A-to-I Human chr11 + 66633317 66633317 66633317 TTGGCTCACTGCAGCCTCTGCCTCCTGAGCTCAGGTGATTCTCCCACCTCAGCCTCCCAAGTGGC TTGGCTCACTGCAGCCTCTGCCTCCTGAGCTCTGGTGATTCTCCCACCTCAGCCTCCCAAGTGGC A T RBM14-RBM4 Ensembl:ENSG00000248643 Protein coding intron GSE107867 ASD brains,frontal_cortex;ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1443985044 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117738,RMVar_hsa_circ_150921 3674 RMVar_ID_3674 Human_SNP_ID_470355974 A-to-I Human chr11 + 66633357 66633357 66633357 CTCCCACCTCAGCCTCCCAAGTGGCTGGAACTACAGGTGTGCACCACCACACCCAGCTAATTTTT CTCCCACCTCAGCCTCCCAAGTGGCTGGAACTGCAGGTGTGCACCACCACACCCAGCTAATTTTT A G RBM14-RBM4 Ensembl:ENSG00000248643 Protein coding intron GSE100210;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229 RNA-Seq:(High) rs1453944818 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117738,RMVar_hsa_circ_150921 3675 RMVar_ID_3675 Human_SNP_ID_470355981 A-to-I Human chr11 + 66633375 66633375 66633375 AAGTGGCTGGAACTACAGGTGTGCACCACCACACCCAGCTAATTTTTTTGTATTTTTAGTAGAGA AAGTGGCTGGAACTACAGGTGTGCACCACCACGCCCAGCTAATTTTTTTGTATTTTTAGTAGAGA A G RBM14-RBM4 Ensembl:ENSG00000248643 Protein coding intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1399356753 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117738,RMVar_hsa_circ_150921 3676 RMVar_ID_3676 Human_SNP_ID_470356006 A-to-I Human chr11 + 66633479 66633479 66633479 ACCTGCCTTGACCTCCCAAAGTGCCGGGATTGAAGGCATGAGACACTGTGCCCGACCAACAAGGT ACCTGCCTTGACCTCCCAAAGTGCCGGGATTGCAGGCATGAGACACTGTGCCCGACCAACAAGGT A C RBM14-RBM4 Ensembl:ENSG00000248643 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1240677718 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11681581,Human_RBP_ID_17560016 RMVar_hsa_circ_117738,RMVar_hsa_circ_150921 3677 RMVar_ID_3677 Human_SNP_ID_470356038 A-to-I Human chr11 + 66633596 66633596 66633596 GCACTTTGGGAGGCTGAGGCGGGTGGATCACCAGAGGTCTGGAGTTTGACACCAGCCTGGCCAAC GCACTTTGGGAGGCTGAGGCGGGTGGATCACCGGAGGTCTGGAGTTTGACACCAGCCTGGCCAAC A G RBM14-RBM4 Ensembl:ENSG00000248643 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1409182830 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17560017 RMVar_hsa_circ_117738,RMVar_hsa_circ_150921 3678 RMVar_ID_3678 Human_SNP_ID_470356093 A-to-I Human chr11 + 66633767 66633767 66633767 CCCGGAGGTGGAGGTTTTCTGTGAGCCGAGATAGTGCCATTGCACTCCAGCCTGGGCAACAAGTG CCCGGAGGTGGAGGTTTTCTGTGAGCCGAGATGGTGCCATTGCACTCCAGCCTGGGCAACAAGTG A G RBM14-RBM4 Ensembl:ENSG00000248643 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1321705959 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23305179 RMVar_hsa_circ_117738,RMVar_hsa_circ_150921 3679 RMVar_ID_3679 Human_SNP_ID_470356137 A-to-I Human chr11 + 66633915 66633907 66633915 TTGGATCAGATCTCTTTAATTGGCCTTTATTTATTTATTTATTTTTTGAGACAGAGTTTTGCTCT TTGGATCAGATCTCTTTAATTGGCC________TTTATTTATTTTTTGAGACAGAGTTTTGCTCT CTTTATTTA C RBM14-RBM4 Ensembl:ENSG00000248643 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs972493776 Functional Loss DEL dbSNP153 26..33 33 - - - RMVar_hsa_circ_117738,RMVar_hsa_circ_150921 3680 RMVar_ID_3680 Human_SNP_ID_470356138 A-to-I Human chr11 + 66633915 66633907 66633915 TTGGATCAGATCTCTTTAATTGGCCTTTATTTATTTATTTATTTTTTGAGACAGAGTTTTGCTCT TTGGATCAGATCTCTTTAATTGGCCTTTA____TTTATTTATTTTTTGAGACAGAGTTTTGCTCT CTTTATTTA CTTTA RBM14-RBM4 Ensembl:ENSG00000248643 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs972493776 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_117738,RMVar_hsa_circ_150921 3681 RMVar_ID_3681 Human_SNP_ID_470356149 A-to-I Human chr11 + 66633935 66633934 66633936 TGGCCTTTATTTATTTATTTATTTTTTGAGACAGAGTTTTGCTCTTGTTGCCCAGGCTGGAGTGT TGGCCTTTATTTATTTATTTATTTTTTGAGAC__AGTTTTGCTCTTGTTGCCCAGGCTGGAGTGT CAG C RBM14-RBM4 Ensembl:ENSG00000248643 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs757662003 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_117738,RMVar_hsa_circ_150921 3682 RMVar_ID_3682 Human_SNP_ID_470356493 A-to-I Human chr11 + 66635153 66635153 66635153 GGGATTACAGGCATGCGCCACCACGTCCACCTAATTTTGTATTTTTAGTAGAGACGGGGTTTCTC GGGATTACAGGCATGCGCCACCACGTCCACCTTATTTTGTATTTTTAGTAGAGACGGGGTTTCTC A T RBM14-RBM4 Ensembl:ENSG00000248643 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1170791104 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117738,RMVar_hsa_circ_150921 3683 RMVar_ID_3683 Human_SNP_ID_470356494 A-to-I Human chr11 + 66635161 66635161 66635161 AGGCATGCGCCACCACGTCCACCTAATTTTGTATTTTTAGTAGAGACGGGGTTTCTCCATGTTGG AGGCATGCGCCACCACGTCCACCTAATTTTGTGTTTTTAGTAGAGACGGGGTTTCTCCATGTTGG A G RBM14-RBM4 Ensembl:ENSG00000248643 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs981489468 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117738,RMVar_hsa_circ_150921 3684 RMVar_ID_3684 Human_SNP_ID_470356608 A-to-I Human chr11 + 66635494 66635494 66635494 GTGGAAGTGTGCGCCTGTAATCCCAGCTACTTAGGAGGCCGAGGCAGGAGAATTGCTTGAACCTG GTGGAAGTGTGCGCCTGTAATCCCAGCTACTTTGGAGGCCGAGGCAGGAGAATTGCTTGAACCTG A T RBM14-RBM4 Ensembl:ENSG00000248643 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,frontal_cortex - 29129909,30559470 RNA-Seq:(High) rs1226311906 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117738,RMVar_hsa_circ_150921 3685 RMVar_ID_3685 Human_SNP_ID_470356797 A-to-I Human chr11 + 66636127 66636127 66636127 CGCCCCCACGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCTGGTAGCTGGGATTACAGGCGCGTG CGCCCCCACGGTTCAAGCAATTCTCCTGCCTCGGCCTCCCTGGTAGCTGGGATTACAGGCGCGTG A G RBM14-RBM4 Ensembl:ENSG00000248643 Protein coding intron GSE47997;GSE38233;GSE100210;GSE107867 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 23474544,24183664,29129909,30559470 RNA-Seq:(High) rs758935939 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117738,RMVar_hsa_circ_150921 3686 RMVar_ID_3686 Human_SNP_ID_470356824 A-to-I Human chr11 + 66636210 66636210 66636210 TTTTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGACATGCTGGTTTTGAACTCCTAA TTTTTTTGTATTTTTAGTAGAGACAGGGTTTCCCCATGTTGGACATGCTGGTTTTGAACTCCTAA A C RBM14-RBM4 Ensembl:ENSG00000248643 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1178583665 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17560018 RMVar_hsa_circ_117738,RMVar_hsa_circ_150921 3687 RMVar_ID_3687 Human_SNP_ID_470356832 A-to-I Human chr11 + 66636241 66636241 66636241 CACCATGTTGGACATGCTGGTTTTGAACTCCTAACCTCAGGTGATCTGCCCACCTCGGCCTCCCA CACCATGTTGGACATGCTGGTTTTGAACTCCTGACCTCAGGTGATCTGCCCACCTCGGCCTCCCA A G RBM14-RBM4 Ensembl:ENSG00000248643 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1028580861 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8356684,Human_RBP_ID_17560018 RMVar_hsa_circ_117738,RMVar_hsa_circ_150921 3688 RMVar_ID_3688 Human_SNP_ID_470356896 A-to-I Human chr11 + 66636393 66636393 66636393 AAGAGTTCGTCTCTATAATAAATTAAAAAAATAGAGAGGCCTGGTGGCACACACGTGTAGTCACA AAGAGTTCGTCTCTATAATAAATTAAAAAAATCGAGAGGCCTGGTGGCACACACGTGTAGTCACA A C RBM14-RBM4 Ensembl:ENSG00000248643 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1379373370 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8356685,Human_RBP_ID_9005655,Human_RBP_ID_11681679,Human_RBP_ID_17560381,Human_RBP_ID_24898329 RMVar_hsa_circ_117738,RMVar_hsa_circ_150921 3689 RMVar_ID_3689 Human_SNP_ID_470357135 A-to-I Human chr11 + 66637256 66637256 66637256 GGGGCCTGCCACCACATTGGGCTAATTTTTGTATTTTTAGTGGAGATGGCGTTCACCATGTTGGC GGGGCCTGCCACCACATTGGGCTAATTTTTGTCTTTTTAGTGGAGATGGCGTTCACCATGTTGGC A C RBM14-RBM4 Ensembl:ENSG00000248643 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1348760468 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6087640,Human_RBP_ID_11681737,Human_RBP_ID_19662788 RMVar_hsa_circ_117738,RMVar_hsa_circ_150921 3690 RMVar_ID_3690 Human_SNP_ID_470357139 A-to-I Human chr11 + 66637281 66637281 66637281 TTTTTGTATTTTTAGTGGAGATGGCGTTCACCATGTTGGCTAGGCTGGTCTTGAACTCCTGACCT TTTTTGTATTTTTAGTGGAGATGGCGTTCACCGTGTTGGCTAGGCTGGTCTTGAACTCCTGACCT A G RBM14-RBM4 Ensembl:ENSG00000248643 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1337858700 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11681738,Human_RBP_ID_18478688 RMVar_hsa_circ_117738,RMVar_hsa_circ_150921 3691 RMVar_ID_3691 Human_SNP_ID_470357158 A-to-I Human chr11 + 66637341 66637341 66637341 GACCTCAGGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGGGCCACCGCA GACCTCAGGTGATCCGCCCGCCTCGGCCTCCCGAAGTGCTGGGATTACAGGCGTGGGCCACCGCA A G RBM14-RBM4 Ensembl:ENSG00000248643 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs765456357 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117738,RMVar_hsa_circ_150921 3692 RMVar_ID_3692 Human_SNP_ID_470360602 A-to-I Human chr11 + 66648296 66648296 66648296 TAATCCCAGCACTTTTGGAGGCTGAGGCAAGCAGGTTGTTTGAGCTCAGGAGTTCAAGACCAGCC TAATCCCAGCACTTTTGGAGGCTGAGGCAAGCTGGTTGTTTGAGCTCAGGAGTTCAAGACCAGCC A T RBM4 Ensembl:ENSG00000173933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934048693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6087823,Human_RBP_ID_11682364 3693 RMVar_ID_3693 Human_SNP_ID_470360711 A-to-I Human chr11 + 66648662 66648661 66648663 CTTGGTGAAACCCCATCTCTACTGAAAAATATAAGTTAGCCGGGCATGGTGGCAGGCGCCTTAAT CTTGGTGAAACCCCATCTCTACTGAAAAATAT__GTTAGCCGGGCATGGTGGCAGGCGCCTTAAT TAA T RBM4 Ensembl:ENSG00000173933 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1201023908 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_9645503,Human_RBP_ID_11682389 3694 RMVar_ID_3694 Human_SNP_ID_470360717 A-to-I Human chr11 + 66648675 66648675 66648675 CATCTCTACTGAAAAATATAAGTTAGCCGGGCATGGTGGCAGGCGCCTTAATTGTGGCTATTTGG CATCTCTACTGAAAAATATAAGTTAGCCGGGCGTGGTGGCAGGCGCCTTAATTGTGGCTATTTGG A G RBM4 Ensembl:ENSG00000173933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1198934584 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11682390 3695 RMVar_ID_3695 Human_SNP_ID_470360869 A-to-I Human chr11 + 66649224 66649224 66649224 AGATGGAGTTTCACCATGGCCAAGCTGGTCTCAAACTCCTGGACTCAAGTGATCCGCCTGCCTCC AGATGGAGTTTCACCATGGCCAAGCTGGTCTCCAACTCCTGGACTCAAGTGATCCGCCTGCCTCC A C RBM4 Ensembl:ENSG00000173933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs964301762 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11682421 3696 RMVar_ID_3696 Human_SNP_ID_470361040 A-to-I Human chr11 + 66649811 66649810 66649811 GTAGCTCACTGTAACTTTGAACTCCTGAGCTCAAGGGATCCTCCCGCCTTGGCCTCCCAGAGTTT GTAGCTCACTGTAACTTTGAACTCCTGAGCTC_AGGGATCCTCCCGCCTTGGCCTCCCAGAGTTT CA C RBM4 Ensembl:ENSG00000173933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1448817671 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_401725,Human_RBP_ID_11682457 Human_Splice_Rec_1263732 3697 RMVar_ID_3697 Human_SNP_ID_470361539 A-to-I Human chr11 + 66651487 66651487 66651487 CTCCTGCCTCACCATCCAGAGTAACTGGGACTACAGGCGCCCGCCACCACACCTGGCTAATTTTT CTCCTGCCTCACCATCCAGAGTAACTGGGACTGCAGGCGCCCGCCACCACACCTGGCTAATTTTT A G RBM4 Ensembl:ENSG00000173933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264787271 Functional Loss SNV dbSNP153 33..33 33 - - - 3698 RMVar_ID_3698 Human_SNP_ID_470362050 A-to-I Human chr11 + 66653436 66653436 66653436 CAGGCTGGAGTGCAGTGATGCGATCTCGGCTCACTGCAACCTCTGCTTCTTGGGTCCAAGCAAAT CAGGCTGGAGTGCAGTGATGCGATCTCGGCTCGCTGCAACCTCTGCTTCTTGGGTCCAAGCAAAT A G RBM4 Ensembl:ENSG00000173933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs948752055 Functional Loss SNV dbSNP153 33..33 33 - - - 3699 RMVar_ID_3699 Human_SNP_ID_470362081 A-to-I Human chr11 + 66653551 66653551 66653551 GCCCAGCTTACTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATATTGGTGAGGCTGTTCTCGA GCCCAGCTTACTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATATTGGTGAGGCTGTTCTCGA A G RBM4 Ensembl:ENSG00000173933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1216431931 Functional Loss SNV dbSNP153 33..33 33 - - - 3700 RMVar_ID_3700 Human_SNP_ID_470363128 A-to-I Human chr11 + 66657312 66657312 66657312 CTAATTTATTTTTTATTTTTATCTTTTGGTAGAGATGGGGTCTCCCTATGTTGCCCAGGCTGGTT CTAATTTATTTTTTATTTTTATCTTTTGGTAGGGATGGGGTCTCCCTATGTTGCCCAGGCTGGTT A G RBM4 Ensembl:ENSG00000173933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs952026346 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17560383 RMVar_hsa_circ_150930 3701 RMVar_ID_3701 Human_SNP_ID_470363200 A-to-I Human chr11 + 66657589 66657589 66657589 CCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGAAGAATCACTTGAACCCGGGAGGTGGAGGGT CCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCGGAAGAATCACTTGAACCCGGGAGGTGGAGGGT A G RBM4 Ensembl:ENSG00000173933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559656349 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150930 3702 RMVar_ID_3702 Human_SNP_ID_470363325 A-to-I Human chr11 + 66657972 66657972 66657972 GAACTCCTGAGCTCTAGCCATTTGCCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG GAACTCCTGAGCTCTAGCCATTTGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG A G RBM4 Ensembl:ENSG00000173933 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1178646082 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11682834 RMVar_hsa_circ_150930 3703 RMVar_ID_3703 Human_SNP_ID_470364650 A-to-I Human chr11 + 66662665 66662665 66662665 GCTCGGGCAATCCACCTGCCTCAGCCTCCCAAAATGCTAGGATTACAGGCGTGAGTCACGCACCT GCTCGGGCAATCCACCTGCCTCAGCCTCCCAAGATGCTAGGATTACAGGCGTGAGTCACGCACCT A G RBM4 Ensembl:ENSG00000173933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1324612095 Functional Loss SNV dbSNP153 33..33 33 - - - 3704 RMVar_ID_3704 Human_SNP_ID_470369075 A-to-I Human chr11 + 66678801 66678801 66678801 CACGAGTTCAGGAGTTCGACACCAGCTTGGCCAACATGGTGAAACCCCGTGTCTACTAAAAATAC CACGAGTTCAGGAGTTCGACACCAGCTTGGCCCACATGGTGAAACCCCGTGTCTACTAAAAATAC A C lnc-RBM4-2,lnc-RBM4-2:2 RNACentral:URS0000D5B40A,RNACentral:URS00008B966F lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1405498138 Functional Loss SNV dbSNP153 33..33 33 - - - 3705 RMVar_ID_3705 Human_SNP_ID_470370075 A-to-I Human chr11 - 66682797 66682795 66682797 GATCATGCCACTGCACTCCAGTCTAGGCAATAAAGTGAGACCCTGTCTCAAAAAAAAAAAAATAG GATCATGCCACTGCACTCCAGTCTAGGCAATA__GTGAGACCCTGTCTCAAAAAAAAAAAAATAG CTT C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1349263913 Functional Loss DEL dbSNP153 33..34 33 - - - 3706 RMVar_ID_3706 Human_SNP_ID_470370116 A-to-I Human chr11 - 66682973 66682973 66682973 GAGGTGAGTGGGTCACTTGAGCTCAGGAGTTCAAGACCAGCCTGGGCAACATGGTGAAACCCCAT GAGGTGAGTGGGTCACTTGAGCTCAGGAGTTCGAGACCAGCCTGGGCAACATGGTGAAACCCCAT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1239294746 Functional Loss SNV dbSNP153 33..33 33 - - - 3707 RMVar_ID_3707 Human_SNP_ID_470370509 A-to-I Human chr11 - 66684454 66684451 66684455 AGTCTGTTTGTTTTTTGTAGAGACGGGGTCTCACTATGTTGCCCAGGTCGGTCTCGAATTCCTGG AGTCTGTTTGTTTTTTGTAGAGACGGGGTCT____ATGTTGCCCAGGTCGGTCTCGAATTCCTGG TAGTG T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006840377 Functional Loss DEL dbSNP153 32..35 33 - - - 3708 RMVar_ID_3708 Human_SNP_ID_470370527 A-to-I Human chr11 - 66684513 66684509 66684513 CTCCCACCTCAGCCTCCCGAGTAGCCTGAACCACAGGCACATGCCATCATACCCGACTAAGTCTG CTCCCACCTCAGCCTCCCGAGTAGCCTGAACC____GCACATGCCATCATACCCGACTAAGTCTG CCTGT C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs199571855 Functional Loss DEL dbSNP153 33..36 33 - - - 3709 RMVar_ID_3709 Human_SNP_ID_470370528 A-to-I Human chr11 - 66684513 66684513 66684513 CTCCCACCTCAGCCTCCCGAGTAGCCTGAACCACAGGCACATGCCATCATACCCGACTAAGTCTG CTCCCACCTCAGCCTCCCGAGTAGCCTGAACCGCAGGCACATGCCATCATACCCGACTAAGTCTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474410099 Functional Loss SNV dbSNP153 33..33 33 - - - 3710 RMVar_ID_3710 Human_SNP_ID_470370540 A-to-I Human chr11 - 66684548 66684548 66684548 CCATTGCAACCTCCACCTCCTGGGTTCAAGCAATCCTCCCACCTCAGCCTCCCGAGTAGCCTGAA CCATTGCAACCTCCACCTCCTGGGTTCAAGCAGTCCTCCCACCTCAGCCTCCCGAGTAGCCTGAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs780061698 Functional Loss SNV dbSNP153 33..33 33 - - - 3711 RMVar_ID_3711 Human_SNP_ID_470374437 A-to-I Human chr11 - 66696485 66696485 66696485 GAAGCCAGAGCTGAAAGCCCTGGTGTCGGAGAAGCTGAGAGACCTGCACAGGCGCTGGGACGAGC GAAGCCAGAGCTGAAAGCCCTGGTGTCGGAGAGGCTGAGAGACCTGCACAGGCGCTGGGACGAGC T C SPTBN2 Ensembl:ENSG00000173898 Protein coding exon GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1449270869 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8356864,Human_RBP_ID_8771311 Human_Splice_Rec_1263814,Human_Splice_Rec_1263888,Human_Splice_Rec_1263960,Human_Splice_Rec_1264074,Human_Splice_Rec_1264166 RMVar_hsa_circ_70940,RMVar_hsa_circ_85085,RMVar_hsa_circ_123670,RMVar_hsa_circ_150935,RMVar_hsa_circ_150936 3712 RMVar_ID_3712 Human_SNP_ID_470381954 A-to-I Human chr11 - 66723362 66723362 66723362 TCCAGACCTCCTTCCTTCCAGAACCCGAGACTACCGAGACTACAGCCCTGGTCCTAGGAAGTAGG TCCAGACCTCCTTCCTTCCAGAACCCGAGACTGCCGAGACTACAGCCCTGGTCCTAGGAAGTAGG T C SPTBN2 Ensembl:ENSG00000173898 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs550370661 Functional Loss SNV dbSNP153 33..33 33 - - - 3713 RMVar_ID_3713 Human_SNP_ID_470381973 A-to-I Human chr11 - 66723427 66723410 66723428 CTGCCTTTGTGTGCCCATGAGTCTCACCACCTACCTGAGTCTCACCACCCAGCACTTCTCTATTC CTGCCTTTGTGTGCCCATGAGTCTCACCACC__________________CAGCACTTCTCTATTC GGGTGGTGAGACTCAGGTA G SPTBN2 Ensembl:ENSG00000173898 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1431224294 Functional Loss DEL dbSNP153 32..49 33 - - - 3714 RMVar_ID_3714 Human_SNP_ID_470382244 A-to-I Human chr11 - 66724749 66724749 66724749 CAAAGGCAGAACCTTTCTGGCTTCCATCATTAACTGGTTCCATGAAGCTGAACCTGACCTGCTTG CAAAGGCAGAACCTTTCTGGCTTCCATCATTAGCTGGTTCCATGAAGCTGAACCTGACCTGCTTG T C SPTBN2 Ensembl:ENSG00000173898 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1194298609 Functional Loss SNV dbSNP153 33..33 33 - - - 3715 RMVar_ID_3715 Human_SNP_ID_470382273 A-to-I Human chr11 - 66724876 66724876 66724876 CTACTTCCTACCACCAGGGCTGTGGTCTTGGCAGTCTCTGGTTCTGGAAAGGAAGGAGGTATGGA CTACTTCCTACCACCAGGGCTGTGGTCTTGGCGGTCTCTGGTTCTGGAAAGGAAGGAGGTATGGA T C SPTBN2 Ensembl:ENSG00000173898 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270338621 Functional Loss SNV dbSNP153 33..33 33 - - - 3716 RMVar_ID_3716 Human_SNP_ID_470382285 A-to-I Human chr11 - 66724936 66724936 66724936 TCCCAGTTGGGCCCCTTTGTAACTTTAACAAAACCCCCAATTCTGCATTTCTCCTGAGCCCTACT TCCCAGTTGGGCCCCTTTGTAACTTTAACAAATCCCCCAATTCTGCATTTCTCCTGAGCCCTACT T A SPTBN2 Ensembl:ENSG00000173898 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1367095701 Functional Loss SNV dbSNP153 33..33 33 - - - 3717 RMVar_ID_3717 Human_SNP_ID_470382288 A-to-I Human chr11 - 66724942 66724942 66724942 TCTGGCTCCCAGTTGGGCCCCTTTGTAACTTTAACAAAACCCCCAATTCTGCATTTCTCCTGAGC TCTGGCTCCCAGTTGGGCCCCTTTGTAACTTTTACAAAACCCCCAATTCTGCATTTCTCCTGAGC T A SPTBN2 Ensembl:ENSG00000173898 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1386327160 Functional Loss SNV dbSNP153 33..33 33 - - - 3718 RMVar_ID_3718 Human_SNP_ID_470387495 A-to-I Human chr11 + 66746045 66746044 66746046 GTTGGCCAGGCTGGTCTTGAACTTCTGACCTCAAGTGATCTGCCCGCCTCCGCCTCCCAAAGTGC GTTGGCCAGGCTGGTCTTGAACTTCTGACCTC__GTGATCTGCCCGCCTCCGCCTCCCAAAGTGC CAA C C11orf80 Ensembl:ENSG00000173715 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1221304309 Functional Loss DEL dbSNP153 33..34 33 - - - 3719 RMVar_ID_3719 Human_SNP_ID_470387937 A-to-I Human chr11 + 66747718 66747717 66747719 AGGGCTCACTTCAGCCTCAATCTTATGGGCTCAAGAGATCATCCTGCCTCAGCCTCCCCAGTGGC AGGGCTCACTTCAGCCTCAATCTTATGGGCTC__GAGATCATCCTGCCTCAGCCTCCCCAGTGGC CAA C C11orf80 Ensembl:ENSG00000173715 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334685628 Functional Loss DEL dbSNP153 33..34 33 - - - 3720 RMVar_ID_3720 Human_SNP_ID_470390134 A-to-I Human chr11 + 66756426 66756426 66756426 GCAGTCTCGGCTCACTGCAACCTCCACCTCCCAGGTTCAAGTGATTCTCATGCCTCAGTCCCCCG GCAGTCTCGGCTCACTGCAACCTCCACCTCCCGGGTTCAAGTGATTCTCATGCCTCAGTCCCCCG A G C11orf80 Ensembl:ENSG00000173715 Protein coding 5'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1194971158 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1264180,Human_Splice_Rec_1264181,Human_Splice_Rec_1264196,Human_Splice_Rec_1264197,Human_Splice_Rec_1264314,Human_Splice_Rec_1264315,Human_Splice_Rec_1264344,Human_Splice_Rec_1264345,Human_Splice_Rec_1264367 RMVar_hsa_circ_150946,RMVar_hsa_circ_72370,RMVar_hsa_circ_310218,RMVar_hsa_circ_317358,RMVar_hsa_circ_357601,RMVar_hsa_circ_321508,RMVar_hsa_circ_312564,RMVar_hsa_circ_294950,RMVar_hsa_circ_307988,RMVar_hsa_circ_279115,RMVar_hsa_circ_150948,RMVar_hsa_circ_150950,RMVar_hsa_circ_150951,RMVar_hsa_circ_150949,RMVar_hsa_circ_150947 3721 RMVar_ID_3721 Human_SNP_ID_470390136 A-to-I Human chr11 + 66756432 66756432 66756432 TCGGCTCACTGCAACCTCCACCTCCCAGGTTCAAGTGATTCTCATGCCTCAGTCCCCCGAGTAGC TCGGCTCACTGCAACCTCCACCTCCCAGGTTCGAGTGATTCTCATGCCTCAGTCCCCCGAGTAGC A G C11orf80 Ensembl:ENSG00000173715 Protein coding 5'UTR GSE99789;GSE107867;GSE123020:GSM3490829,GSM3490830,GSM3490831 esophageal squamous carcinoma cells,EC109;ASD brains,temporal_cortex;esophageal squamous carcinoma cells,EC109 cell line - 29796672,30559470,32596459 RNA-Seq:(High) rs1474101199 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1264180,Human_Splice_Rec_1264181,Human_Splice_Rec_1264196,Human_Splice_Rec_1264197,Human_Splice_Rec_1264314,Human_Splice_Rec_1264315,Human_Splice_Rec_1264344,Human_Splice_Rec_1264345,Human_Splice_Rec_1264367 RMVar_hsa_circ_150946,RMVar_hsa_circ_72370,RMVar_hsa_circ_310218,RMVar_hsa_circ_317358,RMVar_hsa_circ_357601,RMVar_hsa_circ_321508,RMVar_hsa_circ_312564,RMVar_hsa_circ_294950,RMVar_hsa_circ_307988,RMVar_hsa_circ_279115,RMVar_hsa_circ_150948,RMVar_hsa_circ_150950,RMVar_hsa_circ_150951,RMVar_hsa_circ_150949,RMVar_hsa_circ_150947 3722 RMVar_ID_3722 Human_SNP_ID_470390208 A-to-I Human chr11 + 66756789 66756789 66756789 GGTGGAGTGCAGTGGTGCCATCACGGCTCACTACAACCTCTGTTTCCTGGGCTCAGCTGATCTTC GGTGGAGTGCAGTGGTGCCATCACGGCTCACTGCAACCTCTGTTTCCTGGGCTCAGCTGATCTTC A G C11orf80 Ensembl:ENSG00000173715 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1351065837 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150946,RMVar_hsa_circ_72370,RMVar_hsa_circ_310218,RMVar_hsa_circ_317358,RMVar_hsa_circ_357601,RMVar_hsa_circ_321508,RMVar_hsa_circ_312564,RMVar_hsa_circ_294950,RMVar_hsa_circ_307988,RMVar_hsa_circ_279115,RMVar_hsa_circ_150948,RMVar_hsa_circ_150950,RMVar_hsa_circ_150951,RMVar_hsa_circ_150949,RMVar_hsa_circ_150947,RMVar_hsa_circ_150952,RMVar_hsa_circ_150953 3723 RMVar_ID_3723 Human_SNP_ID_470390313 A-to-I Human chr11 + 66757220 66757220 66757220 CAAAAATTAGTCGGGCGCGGTGGCGTATGTCTATAATCCCAGCTACCCAGGAGGCTGAGGCAGGA CAAAAATTAGTCGGGCGCGGTGGCGTATGTCTGTAATCCCAGCTACCCAGGAGGCTGAGGCAGGA A G C11orf80 Ensembl:ENSG00000173715 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs931131376 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150946,RMVar_hsa_circ_72370,RMVar_hsa_circ_310218,RMVar_hsa_circ_317358,RMVar_hsa_circ_357601,RMVar_hsa_circ_321508,RMVar_hsa_circ_312564,RMVar_hsa_circ_294950,RMVar_hsa_circ_307988,RMVar_hsa_circ_279115,RMVar_hsa_circ_150948,RMVar_hsa_circ_150950,RMVar_hsa_circ_150951,RMVar_hsa_circ_150949,RMVar_hsa_circ_150947,RMVar_hsa_circ_150952,RMVar_hsa_circ_150953 3724 RMVar_ID_3724 Human_SNP_ID_470390941 A-to-I Human chr11 + 66759749 66759749 66759749 GGGACTACAGTTGCATGCTGCCACACCCAGCTAATTTTTTGTATCTTAGTAGAGATGGGGTTTCA GGGACTACAGTTGCATGCTGCCACACCCAGCTGATTTTTTGTATCTTAGTAGAGATGGGGTTTCA A G C11orf80 Ensembl:ENSG00000173715 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1248875193 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150955,RMVar_hsa_circ_72370,RMVar_hsa_circ_310218,RMVar_hsa_circ_317358,RMVar_hsa_circ_357601,RMVar_hsa_circ_321508,RMVar_hsa_circ_294950,RMVar_hsa_circ_307988,RMVar_hsa_circ_279115,RMVar_hsa_circ_150948,RMVar_hsa_circ_150950,RMVar_hsa_circ_150951,RMVar_hsa_circ_150949,RMVar_hsa_circ_150947,RMVar_hsa_circ_274651,RMVar_hsa_circ_336385,RMVar_hsa_circ_150953,RMVar_hsa_circ_345505,RMVar_hsa_circ_377429,RMVar_hsa_circ_344408,RMVar_hsa_circ_309700,RMVar_hsa_circ_320889,RMVar_hsa_circ_307201,RMVar_hsa_circ_17767,RMVar_hsa_circ_28718,RMVar_hsa_circ_150956,RMVar_hsa_circ_150954 3725 RMVar_ID_3725 Human_SNP_ID_470391136 A-to-I Human chr11 + 66760537 66760537 66760537 ACAGTGGCTCATGCCTGTAATCCCAGCACTTTAGGAGGCCAAGGCAGGCGGATTGCTTGATCCAG ACAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGCGGATTGCTTGATCCAG A G C11orf80 Ensembl:ENSG00000173715 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1469750876 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150955,RMVar_hsa_circ_72370,RMVar_hsa_circ_310218,RMVar_hsa_circ_317358,RMVar_hsa_circ_357601,RMVar_hsa_circ_321508,RMVar_hsa_circ_294950,RMVar_hsa_circ_307988,RMVar_hsa_circ_279115,RMVar_hsa_circ_150948,RMVar_hsa_circ_150950,RMVar_hsa_circ_150951,RMVar_hsa_circ_150949,RMVar_hsa_circ_150947,RMVar_hsa_circ_274651,RMVar_hsa_circ_336385,RMVar_hsa_circ_150953,RMVar_hsa_circ_345505,RMVar_hsa_circ_377429,RMVar_hsa_circ_344408,RMVar_hsa_circ_309700,RMVar_hsa_circ_320889,RMVar_hsa_circ_307201,RMVar_hsa_circ_17767,RMVar_hsa_circ_28718,RMVar_hsa_circ_150956,RMVar_hsa_circ_150954 3726 RMVar_ID_3726 Human_SNP_ID_470391847 A-to-I Human chr11 + 66762947 66762947 66762947 TGGAGACAGGCCAGCTGAAGTGTCTCACACCTATAATACCAGCACTTCGGGAGGACAAGATGGAA TGGAGACAGGCCAGCTGAAGTGTCTCACACCTCTAATACCAGCACTTCGGGAGGACAAGATGGAA A C C11orf80 Ensembl:ENSG00000173715 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1346065405 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11684222 RMVar_hsa_circ_150955,RMVar_hsa_circ_72370,RMVar_hsa_circ_310218,RMVar_hsa_circ_317358,RMVar_hsa_circ_357601,RMVar_hsa_circ_321508,RMVar_hsa_circ_294950,RMVar_hsa_circ_307988,RMVar_hsa_circ_279115,RMVar_hsa_circ_150948,RMVar_hsa_circ_150950,RMVar_hsa_circ_150951,RMVar_hsa_circ_150949,RMVar_hsa_circ_336385,RMVar_hsa_circ_345505,RMVar_hsa_circ_377429,RMVar_hsa_circ_344408,RMVar_hsa_circ_309700,RMVar_hsa_circ_320889,RMVar_hsa_circ_307201,RMVar_hsa_circ_17767,RMVar_hsa_circ_28718,RMVar_hsa_circ_150956,RMVar_hsa_circ_327709 3727 RMVar_ID_3727 Human_SNP_ID_470394944 A-to-I Human chr11 + 66776268 66776268 66776268 TTTAGTAGAGATGGGATTCTACCATGTTGGCCAGCCTGGTCTTGAACTCCTGACCTCAAGTGATC TTTAGTAGAGATGGGATTCTACCATGTTGGCCGGCCTGGTCTTGAACTCCTGACCTCAAGTGATC A G C11orf80 Ensembl:ENSG00000173715 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167724180 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150955,RMVar_hsa_circ_72370,RMVar_hsa_circ_310218,RMVar_hsa_circ_317358,RMVar_hsa_circ_357601,RMVar_hsa_circ_321508,RMVar_hsa_circ_294950,RMVar_hsa_circ_307988,RMVar_hsa_circ_279115,RMVar_hsa_circ_150948,RMVar_hsa_circ_150950,RMVar_hsa_circ_150951,RMVar_hsa_circ_150949,RMVar_hsa_circ_336385,RMVar_hsa_circ_345505,RMVar_hsa_circ_377429,RMVar_hsa_circ_344408,RMVar_hsa_circ_309700,RMVar_hsa_circ_320889,RMVar_hsa_circ_307201,RMVar_hsa_circ_17767,RMVar_hsa_circ_28718,RMVar_hsa_circ_150956,RMVar_hsa_circ_327709 3728 RMVar_ID_3728 Human_SNP_ID_470395501 A-to-I Human chr11 + 66778405 66778405 66778405 GGGGGATCTTTTGAGCCCAAGAGGTCAAGGCTACAGTGAGCTGCGATCACAGCACTGCACTCTAG GGGGGATCTTTTGAGCCCAAGAGGTCAAGGCTGCAGTGAGCTGCGATCACAGCACTGCACTCTAG A G C11orf80 Ensembl:ENSG00000173715 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs957819934 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150955,RMVar_hsa_circ_72370,RMVar_hsa_circ_310218,RMVar_hsa_circ_317358,RMVar_hsa_circ_357601,RMVar_hsa_circ_321508,RMVar_hsa_circ_294950,RMVar_hsa_circ_307988,RMVar_hsa_circ_279115,RMVar_hsa_circ_150948,RMVar_hsa_circ_150950,RMVar_hsa_circ_150951,RMVar_hsa_circ_150949,RMVar_hsa_circ_336385,RMVar_hsa_circ_345505,RMVar_hsa_circ_377429,RMVar_hsa_circ_344408,RMVar_hsa_circ_309700,RMVar_hsa_circ_320889,RMVar_hsa_circ_307201,RMVar_hsa_circ_17767,RMVar_hsa_circ_28718,RMVar_hsa_circ_150956,RMVar_hsa_circ_327709 3729 RMVar_ID_3729 Human_SNP_ID_470397976 A-to-I Human chr11 + 66788774 66788774 66788774 GAAAATTTTTTTGGTAGAGATGTGGTCTTGCTATGTCGCACAGTCTGGAGTGCAGTGGCTATTCA GAAAATTTTTTTGGTAGAGATGTGGTCTTGCTGTGTCGCACAGTCTGGAGTGCAGTGGCTATTCA A G C11orf80 Ensembl:ENSG00000173715 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1477256375 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150955,RMVar_hsa_circ_72370,RMVar_hsa_circ_310218,RMVar_hsa_circ_317358,RMVar_hsa_circ_357601,RMVar_hsa_circ_321508,RMVar_hsa_circ_307988,RMVar_hsa_circ_279115,RMVar_hsa_circ_150948,RMVar_hsa_circ_150950,RMVar_hsa_circ_150951,RMVar_hsa_circ_150949,RMVar_hsa_circ_336385,RMVar_hsa_circ_345505,RMVar_hsa_circ_377429,RMVar_hsa_circ_344408,RMVar_hsa_circ_320889,RMVar_hsa_circ_307201,RMVar_hsa_circ_17767,RMVar_hsa_circ_28718,RMVar_hsa_circ_150956,RMVar_hsa_circ_150958,RMVar_hsa_circ_348252,RMVar_hsa_circ_350589,RMVar_hsa_circ_281728 3730 RMVar_ID_3730 Human_SNP_ID_470397988 A-to-I Human chr11 + 66788820 66788820 66788820 GGAGTGCAGTGGCTATTCACAGGTGCAGTCATAGCACACTACAGACTTGAACTCCTGAGCTTAAG GGAGTGCAGTGGCTATTCACAGGTGCAGTCATGGCACACTACAGACTTGAACTCCTGAGCTTAAG A G C11orf80 Ensembl:ENSG00000173715 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1376455086 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150955,RMVar_hsa_circ_72370,RMVar_hsa_circ_310218,RMVar_hsa_circ_317358,RMVar_hsa_circ_357601,RMVar_hsa_circ_321508,RMVar_hsa_circ_307988,RMVar_hsa_circ_279115,RMVar_hsa_circ_150948,RMVar_hsa_circ_150950,RMVar_hsa_circ_150951,RMVar_hsa_circ_150949,RMVar_hsa_circ_336385,RMVar_hsa_circ_345505,RMVar_hsa_circ_377429,RMVar_hsa_circ_344408,RMVar_hsa_circ_320889,RMVar_hsa_circ_307201,RMVar_hsa_circ_17767,RMVar_hsa_circ_28718,RMVar_hsa_circ_150956,RMVar_hsa_circ_150958,RMVar_hsa_circ_348252,RMVar_hsa_circ_350589,RMVar_hsa_circ_281728 3731 RMVar_ID_3731 Human_SNP_ID_470398008 A-to-I Human chr11 + 66788897 66788897 66788897 CTCAGCCTGCCGAGTAGCTGGTAGCTGGGACTACAGGTGGGAACTACTGGCACCTGGCTCTGGTG CTCAGCCTGCCGAGTAGCTGGTAGCTGGGACTGCAGGTGGGAACTACTGGCACCTGGCTCTGGTG A G C11orf80 Ensembl:ENSG00000173715 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs898739078 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150955,RMVar_hsa_circ_72370,RMVar_hsa_circ_310218,RMVar_hsa_circ_317358,RMVar_hsa_circ_357601,RMVar_hsa_circ_321508,RMVar_hsa_circ_307988,RMVar_hsa_circ_279115,RMVar_hsa_circ_150948,RMVar_hsa_circ_150950,RMVar_hsa_circ_150951,RMVar_hsa_circ_150949,RMVar_hsa_circ_336385,RMVar_hsa_circ_345505,RMVar_hsa_circ_377429,RMVar_hsa_circ_344408,RMVar_hsa_circ_320889,RMVar_hsa_circ_307201,RMVar_hsa_circ_17767,RMVar_hsa_circ_28718,RMVar_hsa_circ_150956,RMVar_hsa_circ_150958,RMVar_hsa_circ_348252,RMVar_hsa_circ_350589,RMVar_hsa_circ_281728 3732 RMVar_ID_3732 Human_SNP_ID_470398287 A-to-I Human chr11 + 66790158 66790158 66790158 GCCGGGTGTGGTGGCAGCCTGTAGTCCCAGCTACTCTGGAGGCTGAGGCAGGAGAATGGTGTGAA GCCGGGTGTGGTGGCAGCCTGTAGTCCCAGCTGCTCTGGAGGCTGAGGCAGGAGAATGGTGTGAA A G C11orf80 Ensembl:ENSG00000173715 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs776505587 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150955,RMVar_hsa_circ_72370,RMVar_hsa_circ_310218,RMVar_hsa_circ_317358,RMVar_hsa_circ_357601,RMVar_hsa_circ_321508,RMVar_hsa_circ_307988,RMVar_hsa_circ_279115,RMVar_hsa_circ_150948,RMVar_hsa_circ_150950,RMVar_hsa_circ_150951,RMVar_hsa_circ_150949,RMVar_hsa_circ_336385,RMVar_hsa_circ_345505,RMVar_hsa_circ_377429,RMVar_hsa_circ_344408,RMVar_hsa_circ_320889,RMVar_hsa_circ_307201,RMVar_hsa_circ_17767,RMVar_hsa_circ_28718,RMVar_hsa_circ_150956,RMVar_hsa_circ_150958,RMVar_hsa_circ_348252,RMVar_hsa_circ_350589,RMVar_hsa_circ_281728 3733 RMVar_ID_3733 Human_SNP_ID_470398939 A-to-I Human chr11 + 66793167 66793167 66793167 TGGAGTGCAGTGGCACGATCTCAGCTCACTGCAACCTCCATTCCAGGTTCAAGTGATTCTGGTGT TGGAGTGCAGTGGCACGATCTCAGCTCACTGCTACCTCCATTCCAGGTTCAAGTGATTCTGGTGT A T C11orf80 Ensembl:ENSG00000173715 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs979341925 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150955,RMVar_hsa_circ_72370,RMVar_hsa_circ_310218,RMVar_hsa_circ_317358,RMVar_hsa_circ_357601,RMVar_hsa_circ_321508,RMVar_hsa_circ_307988,RMVar_hsa_circ_279115,RMVar_hsa_circ_150948,RMVar_hsa_circ_150950,RMVar_hsa_circ_150951,RMVar_hsa_circ_150949,RMVar_hsa_circ_336385,RMVar_hsa_circ_345505,RMVar_hsa_circ_377429,RMVar_hsa_circ_344408,RMVar_hsa_circ_320889,RMVar_hsa_circ_307201,RMVar_hsa_circ_17767,RMVar_hsa_circ_28718,RMVar_hsa_circ_150956,RMVar_hsa_circ_150958,RMVar_hsa_circ_348252,RMVar_hsa_circ_350589,RMVar_hsa_circ_281728 3734 RMVar_ID_3734 Human_SNP_ID_470398942 A-to-I Human chr11 + 66793179 66793179 66793179 GCACGATCTCAGCTCACTGCAACCTCCATTCCAGGTTCAAGTGATTCTGGTGTCTTAGCCTCCCA GCACGATCTCAGCTCACTGCAACCTCCATTCCCGGTTCAAGTGATTCTGGTGTCTTAGCCTCCCA A C C11orf80 Ensembl:ENSG00000173715 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924944638 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150955,RMVar_hsa_circ_72370,RMVar_hsa_circ_310218,RMVar_hsa_circ_317358,RMVar_hsa_circ_357601,RMVar_hsa_circ_321508,RMVar_hsa_circ_307988,RMVar_hsa_circ_279115,RMVar_hsa_circ_150948,RMVar_hsa_circ_150950,RMVar_hsa_circ_150951,RMVar_hsa_circ_150949,RMVar_hsa_circ_336385,RMVar_hsa_circ_345505,RMVar_hsa_circ_377429,RMVar_hsa_circ_344408,RMVar_hsa_circ_320889,RMVar_hsa_circ_307201,RMVar_hsa_circ_17767,RMVar_hsa_circ_28718,RMVar_hsa_circ_150956,RMVar_hsa_circ_150958,RMVar_hsa_circ_348252,RMVar_hsa_circ_350589,RMVar_hsa_circ_281728 3735 RMVar_ID_3735 Human_SNP_ID_470399097 A-to-I Human chr11 + 66793645 66793645 66793645 TTTTGTATTTTTAGTAGAGACGGGGTTTCATCATCTTGGCCAGCCCTGGTCTTGAACTCCTGACC TTTTGTATTTTTAGTAGAGACGGGGTTTCATCCTCTTGGCCAGCCCTGGTCTTGAACTCCTGACC A C C11orf80 Ensembl:ENSG00000173715 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs891095870 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11684389 RMVar_hsa_circ_150955,RMVar_hsa_circ_72370,RMVar_hsa_circ_310218,RMVar_hsa_circ_317358,RMVar_hsa_circ_357601,RMVar_hsa_circ_321508,RMVar_hsa_circ_307988,RMVar_hsa_circ_279115,RMVar_hsa_circ_150948,RMVar_hsa_circ_150950,RMVar_hsa_circ_150951,RMVar_hsa_circ_150949,RMVar_hsa_circ_336385,RMVar_hsa_circ_345505,RMVar_hsa_circ_377429,RMVar_hsa_circ_344408,RMVar_hsa_circ_320889,RMVar_hsa_circ_307201,RMVar_hsa_circ_17767,RMVar_hsa_circ_28718,RMVar_hsa_circ_150956,RMVar_hsa_circ_150958,RMVar_hsa_circ_348252,RMVar_hsa_circ_350589,RMVar_hsa_circ_281728 3736 RMVar_ID_3736 Human_SNP_ID_470399144 A-to-I Human chr11 + 66793850 66793850 66793850 CATTAAAAGGCCAGGTGCAGTGGCTTATGTGTAATTCTAGTGCTTTGGGAGGCCAAGGTGGGAGG CATTAAAAGGCCAGGTGCAGTGGCTTATGTGTCATTCTAGTGCTTTGGGAGGCCAAGGTGGGAGG A C C11orf80 Ensembl:ENSG00000173715 Protein coding intron GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-Seq:(High) rs964392657 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150955,RMVar_hsa_circ_72370,RMVar_hsa_circ_310218,RMVar_hsa_circ_317358,RMVar_hsa_circ_357601,RMVar_hsa_circ_321508,RMVar_hsa_circ_307988,RMVar_hsa_circ_279115,RMVar_hsa_circ_150948,RMVar_hsa_circ_150950,RMVar_hsa_circ_150951,RMVar_hsa_circ_150949,RMVar_hsa_circ_336385,RMVar_hsa_circ_345505,RMVar_hsa_circ_377429,RMVar_hsa_circ_344408,RMVar_hsa_circ_320889,RMVar_hsa_circ_307201,RMVar_hsa_circ_17767,RMVar_hsa_circ_28718,RMVar_hsa_circ_150956,RMVar_hsa_circ_150958,RMVar_hsa_circ_348252,RMVar_hsa_circ_350589,RMVar_hsa_circ_281728 3737 RMVar_ID_3737 Human_SNP_ID_470399157 A-to-I Human chr11 + 66793924 66793921 66793924 GGCCAAGAGTTTGAGACCAGCCTGGGCAACATAATGAGACCCTGTCTCTACAGAAAATTAAAAAA GGCCAAGAGTTTGAGACCAGCCTGGGCAAC___ATGAGACCCTGTCTCTACAGAAAATTAAAAAA CATA C C11orf80 Ensembl:ENSG00000173715 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1339877536 Functional Loss DEL dbSNP153 31..33 33 - - - RMVar_hsa_circ_150955,RMVar_hsa_circ_72370,RMVar_hsa_circ_310218,RMVar_hsa_circ_317358,RMVar_hsa_circ_357601,RMVar_hsa_circ_321508,RMVar_hsa_circ_307988,RMVar_hsa_circ_279115,RMVar_hsa_circ_150948,RMVar_hsa_circ_150950,RMVar_hsa_circ_150951,RMVar_hsa_circ_150949,RMVar_hsa_circ_336385,RMVar_hsa_circ_345505,RMVar_hsa_circ_377429,RMVar_hsa_circ_344408,RMVar_hsa_circ_320889,RMVar_hsa_circ_307201,RMVar_hsa_circ_17767,RMVar_hsa_circ_28718,RMVar_hsa_circ_150956,RMVar_hsa_circ_150958,RMVar_hsa_circ_348252,RMVar_hsa_circ_350589,RMVar_hsa_circ_281728 3738 RMVar_ID_3738 Human_SNP_ID_470399180 A-to-I Human chr11 + 66794094 66794093 66794094 TGATCATGCCACTGCATTCCAGCCTGAGTGACAAAGCGAGACCCTGTTTCTAAAAAAAAAAAAAA TGATCATGCCACTGCATTCCAGCCTGAGTGAC_AAGCGAGACCCTGTTTCTAAAAAAAAAAAAAA CA C C11orf80 Ensembl:ENSG00000173715 Protein coding intron GSE100210;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229 RNA-Seq:(High) rs1230758846 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_150955,RMVar_hsa_circ_72370,RMVar_hsa_circ_310218,RMVar_hsa_circ_317358,RMVar_hsa_circ_357601,RMVar_hsa_circ_321508,RMVar_hsa_circ_307988,RMVar_hsa_circ_279115,RMVar_hsa_circ_150948,RMVar_hsa_circ_150950,RMVar_hsa_circ_150951,RMVar_hsa_circ_150949,RMVar_hsa_circ_336385,RMVar_hsa_circ_345505,RMVar_hsa_circ_377429,RMVar_hsa_circ_344408,RMVar_hsa_circ_320889,RMVar_hsa_circ_307201,RMVar_hsa_circ_17767,RMVar_hsa_circ_28718,RMVar_hsa_circ_150956,RMVar_hsa_circ_150958,RMVar_hsa_circ_348252,RMVar_hsa_circ_350589,RMVar_hsa_circ_281728 3739 RMVar_ID_3739 Human_SNP_ID_470401905 A-to-I Human chr11 + 66805111 66805111 66805111 TTAATTAAAGCCAGGCGTGGTGGTGTACGCCTATAGTCCCATCTACTTGGGAGGCTGAGGCAGGA TTAATTAAAGCCAGGCGTGGTGGTGTACGCCTGTAGTCCCATCTACTTGGGAGGCTGAGGCAGGA A G C11orf80 Ensembl:ENSG00000173715 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1166267108 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150955,RMVar_hsa_circ_72370,RMVar_hsa_circ_357601,RMVar_hsa_circ_321508,RMVar_hsa_circ_307988,RMVar_hsa_circ_279115,RMVar_hsa_circ_150950,RMVar_hsa_circ_150951,RMVar_hsa_circ_336385,RMVar_hsa_circ_345505,RMVar_hsa_circ_320889,RMVar_hsa_circ_307201,RMVar_hsa_circ_28718,RMVar_hsa_circ_150956,RMVar_hsa_circ_150967,RMVar_hsa_circ_6520,RMVar_hsa_circ_150958,RMVar_hsa_circ_348252,RMVar_hsa_circ_350589,RMVar_hsa_circ_281728,RMVar_hsa_circ_18361,RMVar_hsa_circ_317313,RMVar_hsa_circ_378074,RMVar_hsa_circ_301715,RMVar_hsa_circ_13854,RMVar_hsa_circ_310484,RMVar_hsa_circ_150960,RMVar_hsa_circ_150962,RMVar_hsa_circ_150963,RMVar_hsa_circ_150961,RMVar_hsa_circ_337349,RMVar_hsa_circ_150964,RMVar_hsa_circ_340644,RMVar_hsa_circ_312212,RMVar_hsa_circ_150969,RMVar_hsa_circ_150970,RMVar_hsa_circ_150968,RMVar_hsa_circ_150973,RMVar_hsa_circ_277315,RMVar_hsa_circ_150965,RMVar_hsa_circ_150966,RMVar_hsa_circ_293208,RMVar_hsa_circ_297393,RMVar_hsa_circ_320353,RMVar_hsa_circ_291578,RMVar_hsa_circ_150975,RMVar_hsa_circ_150976,RMVar_hsa_circ_150974,RMVar_hsa_circ_150979,RMVar_hsa_circ_150971,RMVar_hsa_circ_150972,RMVar_hsa_circ_296045,RMVar_hsa_circ_308845,RMVar_hsa_circ_150977,RMVar_hsa_circ_150978 3740 RMVar_ID_3740 Human_SNP_ID_470401992 A-to-I Human chr11 + 66805485 66805485 66805485 GGAGGGGCTTTTTTGTTTTTTTTTTTGGAGACAAGGTCTGGCTCTGTTGCACAGGCCAGAGTGCG GGAGGGGCTTTTTTGTTTTTTTTTTTGGAGACGAGGTCTGGCTCTGTTGCACAGGCCAGAGTGCG A G C11orf80 Ensembl:ENSG00000173715 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1381476853 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150955,RMVar_hsa_circ_72370,RMVar_hsa_circ_357601,RMVar_hsa_circ_321508,RMVar_hsa_circ_307988,RMVar_hsa_circ_279115,RMVar_hsa_circ_150950,RMVar_hsa_circ_150951,RMVar_hsa_circ_336385,RMVar_hsa_circ_345505,RMVar_hsa_circ_320889,RMVar_hsa_circ_307201,RMVar_hsa_circ_28718,RMVar_hsa_circ_150956,RMVar_hsa_circ_150967,RMVar_hsa_circ_6520,RMVar_hsa_circ_150958,RMVar_hsa_circ_348252,RMVar_hsa_circ_350589,RMVar_hsa_circ_281728,RMVar_hsa_circ_18361,RMVar_hsa_circ_317313,RMVar_hsa_circ_378074,RMVar_hsa_circ_301715,RMVar_hsa_circ_13854,RMVar_hsa_circ_310484,RMVar_hsa_circ_150960,RMVar_hsa_circ_150962,RMVar_hsa_circ_150963,RMVar_hsa_circ_150961,RMVar_hsa_circ_337349,RMVar_hsa_circ_150964,RMVar_hsa_circ_340644,RMVar_hsa_circ_312212,RMVar_hsa_circ_150969,RMVar_hsa_circ_150970,RMVar_hsa_circ_150968,RMVar_hsa_circ_150973,RMVar_hsa_circ_277315,RMVar_hsa_circ_150965,RMVar_hsa_circ_150966,RMVar_hsa_circ_293208,RMVar_hsa_circ_297393,RMVar_hsa_circ_320353,RMVar_hsa_circ_291578,RMVar_hsa_circ_150975,RMVar_hsa_circ_150976,RMVar_hsa_circ_150974,RMVar_hsa_circ_150979,RMVar_hsa_circ_150971,RMVar_hsa_circ_150972,RMVar_hsa_circ_296045,RMVar_hsa_circ_308845,RMVar_hsa_circ_150977,RMVar_hsa_circ_150978 3741 RMVar_ID_3741 Human_SNP_ID_470402018 A-to-I Human chr11 + 66805594 66805594 66805594 AACCATCCTCCCACCTCAGCCTCCTAGAGACCACAGGTGCATGCCACCATGCCCAGTTAATTTTT AACCATCCTCCCACCTCAGCCTCCTAGAGACCGCAGGTGCATGCCACCATGCCCAGTTAATTTTT A G C11orf80 Ensembl:ENSG00000173715 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1029816299 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150955,RMVar_hsa_circ_72370,RMVar_hsa_circ_357601,RMVar_hsa_circ_321508,RMVar_hsa_circ_307988,RMVar_hsa_circ_279115,RMVar_hsa_circ_150950,RMVar_hsa_circ_150951,RMVar_hsa_circ_336385,RMVar_hsa_circ_345505,RMVar_hsa_circ_320889,RMVar_hsa_circ_307201,RMVar_hsa_circ_28718,RMVar_hsa_circ_150956,RMVar_hsa_circ_150967,RMVar_hsa_circ_6520,RMVar_hsa_circ_150958,RMVar_hsa_circ_348252,RMVar_hsa_circ_350589,RMVar_hsa_circ_281728,RMVar_hsa_circ_18361,RMVar_hsa_circ_317313,RMVar_hsa_circ_378074,RMVar_hsa_circ_301715,RMVar_hsa_circ_13854,RMVar_hsa_circ_310484,RMVar_hsa_circ_150960,RMVar_hsa_circ_150962,RMVar_hsa_circ_150963,RMVar_hsa_circ_150961,RMVar_hsa_circ_337349,RMVar_hsa_circ_150964,RMVar_hsa_circ_340644,RMVar_hsa_circ_312212,RMVar_hsa_circ_150969,RMVar_hsa_circ_150970,RMVar_hsa_circ_150968,RMVar_hsa_circ_150973,RMVar_hsa_circ_277315,RMVar_hsa_circ_150965,RMVar_hsa_circ_150966,RMVar_hsa_circ_293208,RMVar_hsa_circ_297393,RMVar_hsa_circ_320353,RMVar_hsa_circ_291578,RMVar_hsa_circ_150975,RMVar_hsa_circ_150976,RMVar_hsa_circ_150974,RMVar_hsa_circ_150979,RMVar_hsa_circ_150971,RMVar_hsa_circ_150972,RMVar_hsa_circ_296045,RMVar_hsa_circ_308845,RMVar_hsa_circ_150977,RMVar_hsa_circ_150978 3742 RMVar_ID_3742 Human_SNP_ID_470402240 A-to-I Human chr11 + 66806603 66806603 66806603 CAGCATGGCCAACATGGCAAAACCCTGTCTCTATTAAAAATACAAAAATTAGCTGGACATGGTGG CAGCATGGCCAACATGGCAAAACCCTGTCTCTTTTAAAAATACAAAAATTAGCTGGACATGGTGG A T C11orf80 Ensembl:ENSG00000173715 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1413403348 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150955,RMVar_hsa_circ_72370,RMVar_hsa_circ_357601,RMVar_hsa_circ_321508,RMVar_hsa_circ_307988,RMVar_hsa_circ_279115,RMVar_hsa_circ_150950,RMVar_hsa_circ_150951,RMVar_hsa_circ_336385,RMVar_hsa_circ_345505,RMVar_hsa_circ_320889,RMVar_hsa_circ_307201,RMVar_hsa_circ_28718,RMVar_hsa_circ_150956,RMVar_hsa_circ_150967,RMVar_hsa_circ_6520,RMVar_hsa_circ_150958,RMVar_hsa_circ_348252,RMVar_hsa_circ_350589,RMVar_hsa_circ_281728,RMVar_hsa_circ_18361,RMVar_hsa_circ_317313,RMVar_hsa_circ_378074,RMVar_hsa_circ_301715,RMVar_hsa_circ_13854,RMVar_hsa_circ_310484,RMVar_hsa_circ_150960,RMVar_hsa_circ_150962,RMVar_hsa_circ_150963,RMVar_hsa_circ_150961,RMVar_hsa_circ_337349,RMVar_hsa_circ_150964,RMVar_hsa_circ_340644,RMVar_hsa_circ_312212,RMVar_hsa_circ_150969,RMVar_hsa_circ_150970,RMVar_hsa_circ_150968,RMVar_hsa_circ_150973,RMVar_hsa_circ_277315,RMVar_hsa_circ_150965,RMVar_hsa_circ_150966,RMVar_hsa_circ_293208,RMVar_hsa_circ_297393,RMVar_hsa_circ_320353,RMVar_hsa_circ_291578,RMVar_hsa_circ_150975,RMVar_hsa_circ_150976,RMVar_hsa_circ_150974,RMVar_hsa_circ_150979,RMVar_hsa_circ_150971,RMVar_hsa_circ_150972,RMVar_hsa_circ_296045,RMVar_hsa_circ_308845,RMVar_hsa_circ_150977,RMVar_hsa_circ_150978 3743 RMVar_ID_3743 Human_SNP_ID_470402913 A-to-I Human chr11 + 66809771 66809771 66809771 TGTTGCCCAGGCTAAAGTGCAGTTGTGCGATCATAGCTCACTGCAACCTCGAACTTCTGGGGTTA TGTTGCCCAGGCTAAAGTGCAGTTGTGCGATCGTAGCTCACTGCAACCTCGAACTTCTGGGGTTA A G C11orf80 Ensembl:ENSG00000173715 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1344153854 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150955,RMVar_hsa_circ_72370,RMVar_hsa_circ_357601,RMVar_hsa_circ_321508,RMVar_hsa_circ_307988,RMVar_hsa_circ_279115,RMVar_hsa_circ_150950,RMVar_hsa_circ_150951,RMVar_hsa_circ_336385,RMVar_hsa_circ_345505,RMVar_hsa_circ_320889,RMVar_hsa_circ_307201,RMVar_hsa_circ_28718,RMVar_hsa_circ_150956,RMVar_hsa_circ_150967,RMVar_hsa_circ_6520,RMVar_hsa_circ_150958,RMVar_hsa_circ_348252,RMVar_hsa_circ_350589,RMVar_hsa_circ_281728,RMVar_hsa_circ_18361,RMVar_hsa_circ_317313,RMVar_hsa_circ_378074,RMVar_hsa_circ_301715,RMVar_hsa_circ_13854,RMVar_hsa_circ_310484,RMVar_hsa_circ_150960,RMVar_hsa_circ_150962,RMVar_hsa_circ_150963,RMVar_hsa_circ_150961,RMVar_hsa_circ_337349,RMVar_hsa_circ_150964,RMVar_hsa_circ_340644,RMVar_hsa_circ_312212,RMVar_hsa_circ_150969,RMVar_hsa_circ_150970,RMVar_hsa_circ_150968,RMVar_hsa_circ_150973,RMVar_hsa_circ_277315,RMVar_hsa_circ_150965,RMVar_hsa_circ_150966,RMVar_hsa_circ_293208,RMVar_hsa_circ_297393,RMVar_hsa_circ_320353,RMVar_hsa_circ_291578,RMVar_hsa_circ_150975,RMVar_hsa_circ_150976,RMVar_hsa_circ_150974,RMVar_hsa_circ_150979,RMVar_hsa_circ_150971,RMVar_hsa_circ_150972,RMVar_hsa_circ_296045,RMVar_hsa_circ_308845,RMVar_hsa_circ_150977,RMVar_hsa_circ_150978 3744 RMVar_ID_3744 Human_SNP_ID_470402925 A-to-I Human chr11 + 66809845 66809845 66809845 CCTACCTCAGCCTCTCCTGAGTAGCTGGGACTACAAGCATGCACCATCATGCCTGGCTAATTTTT CCTACCTCAGCCTCTCCTGAGTAGCTGGGACTGCAAGCATGCACCATCATGCCTGGCTAATTTTT A G C11orf80 Ensembl:ENSG00000173715 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1304982615 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150955,RMVar_hsa_circ_72370,RMVar_hsa_circ_357601,RMVar_hsa_circ_321508,RMVar_hsa_circ_307988,RMVar_hsa_circ_279115,RMVar_hsa_circ_150950,RMVar_hsa_circ_150951,RMVar_hsa_circ_336385,RMVar_hsa_circ_345505,RMVar_hsa_circ_320889,RMVar_hsa_circ_307201,RMVar_hsa_circ_28718,RMVar_hsa_circ_150956,RMVar_hsa_circ_150967,RMVar_hsa_circ_6520,RMVar_hsa_circ_150958,RMVar_hsa_circ_348252,RMVar_hsa_circ_350589,RMVar_hsa_circ_281728,RMVar_hsa_circ_18361,RMVar_hsa_circ_317313,RMVar_hsa_circ_378074,RMVar_hsa_circ_301715,RMVar_hsa_circ_13854,RMVar_hsa_circ_310484,RMVar_hsa_circ_150960,RMVar_hsa_circ_150962,RMVar_hsa_circ_150963,RMVar_hsa_circ_150961,RMVar_hsa_circ_337349,RMVar_hsa_circ_150964,RMVar_hsa_circ_340644,RMVar_hsa_circ_312212,RMVar_hsa_circ_150969,RMVar_hsa_circ_150970,RMVar_hsa_circ_150968,RMVar_hsa_circ_150973,RMVar_hsa_circ_277315,RMVar_hsa_circ_150965,RMVar_hsa_circ_150966,RMVar_hsa_circ_293208,RMVar_hsa_circ_297393,RMVar_hsa_circ_320353,RMVar_hsa_circ_291578,RMVar_hsa_circ_150975,RMVar_hsa_circ_150976,RMVar_hsa_circ_150974,RMVar_hsa_circ_150979,RMVar_hsa_circ_150971,RMVar_hsa_circ_150972,RMVar_hsa_circ_296045,RMVar_hsa_circ_308845,RMVar_hsa_circ_150977,RMVar_hsa_circ_150978 3745 RMVar_ID_3745 Human_SNP_ID_470403172 A-to-I Human chr11 + 66811047 66811047 66811047 TTGATCTTAGCTCACTGCAGCCTTGAACTCCTAAGCTCGTGTGACCTTCCCACTTCAGCCTCCTG TTGATCTTAGCTCACTGCAGCCTTGAACTCCTGAGCTCGTGTGACCTTCCCACTTCAGCCTCCTG A G C11orf80 Ensembl:ENSG00000173715 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs939199766 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150955,RMVar_hsa_circ_72370,RMVar_hsa_circ_357601,RMVar_hsa_circ_321508,RMVar_hsa_circ_307988,RMVar_hsa_circ_279115,RMVar_hsa_circ_150950,RMVar_hsa_circ_150951,RMVar_hsa_circ_336385,RMVar_hsa_circ_345505,RMVar_hsa_circ_320889,RMVar_hsa_circ_307201,RMVar_hsa_circ_28718,RMVar_hsa_circ_150956,RMVar_hsa_circ_150967,RMVar_hsa_circ_6520,RMVar_hsa_circ_150958,RMVar_hsa_circ_348252,RMVar_hsa_circ_350589,RMVar_hsa_circ_281728,RMVar_hsa_circ_18361,RMVar_hsa_circ_317313,RMVar_hsa_circ_378074,RMVar_hsa_circ_301715,RMVar_hsa_circ_13854,RMVar_hsa_circ_310484,RMVar_hsa_circ_150960,RMVar_hsa_circ_150962,RMVar_hsa_circ_150963,RMVar_hsa_circ_150961,RMVar_hsa_circ_337349,RMVar_hsa_circ_150964,RMVar_hsa_circ_340644,RMVar_hsa_circ_312212,RMVar_hsa_circ_150969,RMVar_hsa_circ_150970,RMVar_hsa_circ_150968,RMVar_hsa_circ_150973,RMVar_hsa_circ_277315,RMVar_hsa_circ_150965,RMVar_hsa_circ_150966,RMVar_hsa_circ_293208,RMVar_hsa_circ_297393,RMVar_hsa_circ_320353,RMVar_hsa_circ_291578,RMVar_hsa_circ_150975,RMVar_hsa_circ_150976,RMVar_hsa_circ_150974,RMVar_hsa_circ_150979,RMVar_hsa_circ_150971,RMVar_hsa_circ_150972,RMVar_hsa_circ_296045,RMVar_hsa_circ_308845,RMVar_hsa_circ_150977,RMVar_hsa_circ_150978 3746 RMVar_ID_3746 Human_SNP_ID_470403334 A-to-I Human chr11 + 66811868 66811868 66811868 AGGCTGATGCAGAGAGAGGCTCGCTTGAGCACAGGAATTTGAGGCTGCAGTGAGCTATGATCACA AGGCTGATGCAGAGAGAGGCTCGCTTGAGCACGGGAATTTGAGGCTGCAGTGAGCTATGATCACA A G C11orf80 Ensembl:ENSG00000173715 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1184578152 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150955,RMVar_hsa_circ_72370,RMVar_hsa_circ_357601,RMVar_hsa_circ_321508,RMVar_hsa_circ_307988,RMVar_hsa_circ_279115,RMVar_hsa_circ_150950,RMVar_hsa_circ_150951,RMVar_hsa_circ_336385,RMVar_hsa_circ_345505,RMVar_hsa_circ_320889,RMVar_hsa_circ_307201,RMVar_hsa_circ_28718,RMVar_hsa_circ_150956,RMVar_hsa_circ_150967,RMVar_hsa_circ_6520,RMVar_hsa_circ_150958,RMVar_hsa_circ_348252,RMVar_hsa_circ_350589,RMVar_hsa_circ_281728,RMVar_hsa_circ_18361,RMVar_hsa_circ_317313,RMVar_hsa_circ_378074,RMVar_hsa_circ_301715,RMVar_hsa_circ_13854,RMVar_hsa_circ_310484,RMVar_hsa_circ_150960,RMVar_hsa_circ_150962,RMVar_hsa_circ_150963,RMVar_hsa_circ_150961,RMVar_hsa_circ_337349,RMVar_hsa_circ_150964,RMVar_hsa_circ_340644,RMVar_hsa_circ_312212,RMVar_hsa_circ_150969,RMVar_hsa_circ_150970,RMVar_hsa_circ_150968,RMVar_hsa_circ_150973,RMVar_hsa_circ_277315,RMVar_hsa_circ_150965,RMVar_hsa_circ_150966,RMVar_hsa_circ_293208,RMVar_hsa_circ_297393,RMVar_hsa_circ_320353,RMVar_hsa_circ_291578,RMVar_hsa_circ_150975,RMVar_hsa_circ_150976,RMVar_hsa_circ_150974,RMVar_hsa_circ_150979,RMVar_hsa_circ_150971,RMVar_hsa_circ_150972,RMVar_hsa_circ_296045,RMVar_hsa_circ_308845,RMVar_hsa_circ_150977,RMVar_hsa_circ_150978 3747 RMVar_ID_3747 Human_SNP_ID_470403339 A-to-I Human chr11 + 66811892 66811892 66811892 TTGAGCACAGGAATTTGAGGCTGCAGTGAGCTATGATCACATCATTGCACTCCAGTCTGAGCAAC TTGAGCACAGGAATTTGAGGCTGCAGTGAGCTGTGATCACATCATTGCACTCCAGTCTGAGCAAC A G C11orf80 Ensembl:ENSG00000173715 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1193739559 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150955,RMVar_hsa_circ_72370,RMVar_hsa_circ_357601,RMVar_hsa_circ_321508,RMVar_hsa_circ_307988,RMVar_hsa_circ_279115,RMVar_hsa_circ_150950,RMVar_hsa_circ_150951,RMVar_hsa_circ_336385,RMVar_hsa_circ_345505,RMVar_hsa_circ_320889,RMVar_hsa_circ_307201,RMVar_hsa_circ_28718,RMVar_hsa_circ_150956,RMVar_hsa_circ_150967,RMVar_hsa_circ_6520,RMVar_hsa_circ_150958,RMVar_hsa_circ_348252,RMVar_hsa_circ_350589,RMVar_hsa_circ_281728,RMVar_hsa_circ_18361,RMVar_hsa_circ_317313,RMVar_hsa_circ_378074,RMVar_hsa_circ_301715,RMVar_hsa_circ_13854,RMVar_hsa_circ_310484,RMVar_hsa_circ_150960,RMVar_hsa_circ_150962,RMVar_hsa_circ_150963,RMVar_hsa_circ_150961,RMVar_hsa_circ_337349,RMVar_hsa_circ_150964,RMVar_hsa_circ_340644,RMVar_hsa_circ_312212,RMVar_hsa_circ_150969,RMVar_hsa_circ_150970,RMVar_hsa_circ_150968,RMVar_hsa_circ_150973,RMVar_hsa_circ_277315,RMVar_hsa_circ_150965,RMVar_hsa_circ_150966,RMVar_hsa_circ_293208,RMVar_hsa_circ_297393,RMVar_hsa_circ_320353,RMVar_hsa_circ_291578,RMVar_hsa_circ_150975,RMVar_hsa_circ_150976,RMVar_hsa_circ_150974,RMVar_hsa_circ_150979,RMVar_hsa_circ_150971,RMVar_hsa_circ_150972,RMVar_hsa_circ_296045,RMVar_hsa_circ_308845,RMVar_hsa_circ_150977,RMVar_hsa_circ_150978 3748 RMVar_ID_3748 Human_SNP_ID_470403735 A-to-I Human chr11 + 66813479 66813479 66813479 TGCATAGGCTGGGCATGATGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGCAG TGCATAGGCTGGGCATGATGGCTCACGCCTGTCATCCCAGCACTTTGGGAGGCCGAGGTGGGCAG A C C11orf80 Ensembl:ENSG00000173715 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1183731176 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_109805 RMVar_hsa_circ_150955,RMVar_hsa_circ_72370,RMVar_hsa_circ_357601,RMVar_hsa_circ_321508,RMVar_hsa_circ_307988,RMVar_hsa_circ_279115,RMVar_hsa_circ_150950,RMVar_hsa_circ_150951,RMVar_hsa_circ_336385,RMVar_hsa_circ_345505,RMVar_hsa_circ_320889,RMVar_hsa_circ_307201,RMVar_hsa_circ_28718,RMVar_hsa_circ_150956,RMVar_hsa_circ_150967,RMVar_hsa_circ_6520,RMVar_hsa_circ_150958,RMVar_hsa_circ_348252,RMVar_hsa_circ_350589,RMVar_hsa_circ_281728,RMVar_hsa_circ_18361,RMVar_hsa_circ_317313,RMVar_hsa_circ_378074,RMVar_hsa_circ_301715,RMVar_hsa_circ_13854,RMVar_hsa_circ_310484,RMVar_hsa_circ_150960,RMVar_hsa_circ_150962,RMVar_hsa_circ_150963,RMVar_hsa_circ_150961,RMVar_hsa_circ_337349,RMVar_hsa_circ_150964,RMVar_hsa_circ_340644,RMVar_hsa_circ_312212,RMVar_hsa_circ_150969,RMVar_hsa_circ_150970,RMVar_hsa_circ_150968,RMVar_hsa_circ_150973,RMVar_hsa_circ_277315,RMVar_hsa_circ_150965,RMVar_hsa_circ_150966,RMVar_hsa_circ_293208,RMVar_hsa_circ_297393,RMVar_hsa_circ_320353,RMVar_hsa_circ_291578,RMVar_hsa_circ_150975,RMVar_hsa_circ_150976,RMVar_hsa_circ_150974,RMVar_hsa_circ_150979,RMVar_hsa_circ_150971,RMVar_hsa_circ_150972,RMVar_hsa_circ_296045,RMVar_hsa_circ_308845,RMVar_hsa_circ_150977,RMVar_hsa_circ_150978 3749 RMVar_ID_3749 Human_SNP_ID_470408063 A-to-I Human chr11 - 66831839 66831839 66831839 TTGCCTGCCACCATGCCCAGCTAATTTTTTTTATATTTTTAGTAGAGATGGGGTTTCACCATCTT TTGCCTGCCACCATGCCCAGCTAATTTTTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATCTT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1174918588 Functional Loss SNV dbSNP153 33..33 33 - - - 3750 RMVar_ID_3750 Human_SNP_ID_470408071 A-to-I Human chr11 - 66831889 66831889 66831889 GGGTTCAAGCAATTCTCCTGCCTCAGCCACCCAAGTAGTTGGGATTATAGTTGCCTGCCACCATG GGGTTCAAGCAATTCTCCTGCCTCAGCCACCCGAGTAGTTGGGATTATAGTTGCCTGCCACCATG T C lnc-PC-2 RNACentral:URS0000D5D865 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1040278651 Functional Loss SNV dbSNP153 33..33 33 - - - 3751 RMVar_ID_3751 Human_SNP_ID_470408217 A-to-I Human chr11 - 66832262 66832262 66832262 CTCCGTCTTTACTAAAAATAGAAAAAACAATTAGTCGGGCATGGTGGCAGGTGCCTGTAGTCCCA CTCCGTCTTTACTAAAAATAGAAAAAACAATTTGTCGGGCATGGTGGCAGGTGCCTGTAGTCCCA T A lnc-PC-2 RNACentral:URS0000D5D865 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1471770017 Functional Loss SNV dbSNP153 33..33 33 - - - 3752 RMVar_ID_3752 Human_SNP_ID_470408415 A-to-I Human chr11 - 66833077 66833077 66833077 TGCCACTGCACTCCAGTCTGGGCGACAGAGCAAGACTCGGTGTCAAAAAAAAAAAAAAAAAAAAA TGCCACTGCACTCCAGTCTGGGCGACAGAGCAGGACTCGGTGTCAAAAAAAAAAAAAAAAAAAAA T C lnc-PC-2 RNACentral:URS0000D5D865 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1183305229 Functional Loss SNV dbSNP153 33..33 33 - - - 3753 RMVar_ID_3753 Human_SNP_ID_470408459 A-to-I Human chr11 + 66833277 66833277 66833277 TGCCATGTTGGCCAGGCTGGTCTCGAACTCCTAGCCTTAGGTGATCTGGCTGCTTTGGCCTCCCA TGCCATGTTGGCCAGGCTGGTCTCGAACTCCTGGCCTTAGGTGATCTGGCTGCTTTGGCCTCCCA A G C11orf80 Ensembl:ENSG00000173715 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs942179926 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_357601,RMVar_hsa_circ_345505,RMVar_hsa_circ_150956,RMVar_hsa_circ_317313,RMVar_hsa_circ_150963,RMVar_hsa_circ_337349,RMVar_hsa_circ_150969,RMVar_hsa_circ_150970,RMVar_hsa_circ_150979,RMVar_hsa_circ_150971,RMVar_hsa_circ_308845,RMVar_hsa_circ_49163,RMVar_hsa_circ_150981,RMVar_hsa_circ_119590,RMVar_hsa_circ_270738,RMVar_hsa_circ_150982,RMVar_hsa_circ_5443,RMVar_hsa_circ_338982,RMVar_hsa_circ_90981,RMVar_hsa_circ_150991,RMVar_hsa_circ_323658 3754 RMVar_ID_3754 Human_SNP_ID_470408559 A-to-I Human chr11 - 66833731 66833723 66833731 GTTTGCCAGGCAGGTTTCAAACTCCTGACCTCAAGTGATCCACCTGCCTTGCCCTCCCAAAGTGC GTTTGCCAGGCAGGTTTCAAACTCCTGACCTC________CACCTGCCTTGCCCTCCCAAAGTGC GGATCACTT G lnc-PC-2 RNACentral:URS0000D5D865 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1198459609 Functional Loss DEL dbSNP153 33..40 33 - - - 3755 RMVar_ID_3755 Human_SNP_ID_470408775 A-to-I Human chr11 + 66834705 66834705 66834705 TGTTTTTATTTTTTTAGAAACAGGTTCCCGCTATGTTGCCCGGGCTGGAGTGCAGTGACTATTCA TGTTTTTATTTTTTTAGAAACAGGTTCCCGCTCTGTTGCCCGGGCTGGAGTGCAGTGACTATTCA A C C11orf80 Ensembl:ENSG00000173715 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1055364373 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_357601,RMVar_hsa_circ_345505,RMVar_hsa_circ_150956,RMVar_hsa_circ_317313,RMVar_hsa_circ_150963,RMVar_hsa_circ_337349,RMVar_hsa_circ_150969,RMVar_hsa_circ_150970,RMVar_hsa_circ_150979,RMVar_hsa_circ_150971,RMVar_hsa_circ_308845,RMVar_hsa_circ_49163,RMVar_hsa_circ_150981,RMVar_hsa_circ_119590,RMVar_hsa_circ_270738,RMVar_hsa_circ_150982,RMVar_hsa_circ_5443,RMVar_hsa_circ_338982,RMVar_hsa_circ_90981,RMVar_hsa_circ_150991,RMVar_hsa_circ_323658 3756 RMVar_ID_3756 Human_SNP_ID_470408776 A-to-I Human chr11 + 66834705 66834705 66834705 TGTTTTTATTTTTTTAGAAACAGGTTCCCGCTATGTTGCCCGGGCTGGAGTGCAGTGACTATTCA TGTTTTTATTTTTTTAGAAACAGGTTCCCGCTGTGTTGCCCGGGCTGGAGTGCAGTGACTATTCA A G C11orf80 Ensembl:ENSG00000173715 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1055364373 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_357601,RMVar_hsa_circ_345505,RMVar_hsa_circ_150956,RMVar_hsa_circ_317313,RMVar_hsa_circ_150963,RMVar_hsa_circ_337349,RMVar_hsa_circ_150969,RMVar_hsa_circ_150970,RMVar_hsa_circ_150979,RMVar_hsa_circ_150971,RMVar_hsa_circ_308845,RMVar_hsa_circ_49163,RMVar_hsa_circ_150981,RMVar_hsa_circ_119590,RMVar_hsa_circ_270738,RMVar_hsa_circ_150982,RMVar_hsa_circ_5443,RMVar_hsa_circ_338982,RMVar_hsa_circ_90981,RMVar_hsa_circ_150991,RMVar_hsa_circ_323658 3757 RMVar_ID_3757 Human_SNP_ID_470409148 A-to-I Human chr11 + 66836318 66836318 66836318 GGCTCACTGCAAGCTCCACCTCCCGGATTCACACCATTCTCCTGCCTCAAGTAGCTGGGACTTAC GGCTCACTGCAAGCTCCACCTCCCGGATTCACCCCATTCTCCTGCCTCAAGTAGCTGGGACTTAC A C C11orf80 Ensembl:ENSG00000173715 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1045700494 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_357601,RMVar_hsa_circ_345505,RMVar_hsa_circ_150956,RMVar_hsa_circ_317313,RMVar_hsa_circ_150963,RMVar_hsa_circ_337349,RMVar_hsa_circ_150969,RMVar_hsa_circ_150970,RMVar_hsa_circ_150979,RMVar_hsa_circ_150971,RMVar_hsa_circ_308845,RMVar_hsa_circ_49163,RMVar_hsa_circ_150981,RMVar_hsa_circ_119590,RMVar_hsa_circ_270738,RMVar_hsa_circ_150982,RMVar_hsa_circ_5443,RMVar_hsa_circ_338982,RMVar_hsa_circ_90981,RMVar_hsa_circ_150991,RMVar_hsa_circ_323658 3758 RMVar_ID_3758 Human_SNP_ID_470409245 A-to-I Human chr11 - 66836673 66836670 66836674 AAAAATCATATTTTCTGTAGTGACGAGGTCTCACTATGTTGCCCAGGCTGGTCTCAAACTCCTGG AAAAATCATATTTTCTGTAGTGACGAGGTCT____ATGTTGCCCAGGCTGGTCTCAAACTCCTGG TAGTG T lnc-PC-2 RNACentral:URS0000D5D865 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs58307511 Functional Loss DEL dbSNP153 32..35 33 - - - 3759 RMVar_ID_3759 Human_SNP_ID_470409246 A-to-I Human chr11 - 66836670 66836670 66836670 AATCATATTTTCTGTAGTGACGAGGTCTCACTATGTTGCCCAGGCTGGTCTCAAACTCCTGGGCT AATCATATTTTCTGTAGTGACGAGGTCTCACTGTGTTGCCCAGGCTGGTCTCAAACTCCTGGGCT T C lnc-PC-2 RNACentral:URS0000D5D865 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1009191587 Functional Loss SNV dbSNP153 33..33 33 - - - 3760 RMVar_ID_3760 Human_SNP_ID_470410525 A-to-I Human chr11 + 66841699 66841699 66841699 GTTTCTAGCCAGGCAAGGTGGTGTGTGCCTTTAGTCCCAGTTACTCGAGAGGATGAGGCCGGGAG GTTTCTAGCCAGGCAAGGTGGTGTGTGCCTTTCGTCCCAGTTACTCGAGAGGATGAGGCCGGGAG A C C11orf80 Ensembl:ENSG00000173715 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1008244320 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150981,RMVar_hsa_circ_119590,RMVar_hsa_circ_90981,RMVar_hsa_circ_150991 3761 RMVar_ID_3761 Human_SNP_ID_470410599 A-to-I Human chr11 - 66842002 66842002 66842002 AGAGACAGGGGTCTCACCGTGTTGCCCAGGCTAGTCTCAAGCTGTCCTCCCGCCCCAGCTCCCCA AGAGACAGGGGTCTCACCGTGTTGCCCAGGCTGGTCTCAAGCTGTCCTCCCGCCCCAGCTCCCCA T C lnc-PC-2 RNACentral:URS0000D5D865 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1371221405 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11684548 3762 RMVar_ID_3762 Human_SNP_ID_470410605 A-to-I Human chr11 - 66842019 66842019 66842019 TAATTTTTTTTACTTGTAGAGACAGGGGTCTCACCGTGTTGCCCAGGCTAGTCTCAAGCTGTCCT TAATTTTTTTTACTTGTAGAGACAGGGGTCTCCCCGTGTTGCCCAGGCTAGTCTCAAGCTGTCCT T G lnc-PC-2 RNACentral:URS0000D5D865 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs771939186 Functional Loss SNV dbSNP153 33..33 33 - - - 3763 RMVar_ID_3763 Human_SNP_ID_470410632 A-to-I Human chr11 + 66842128 66842128 66842128 CTGAAGCTGAGGCAGTAGGATCGCTTGAGCCCAGGAGGTCGAGGCTGCAGTGAGCCAGGACTGAG CTGAAGCTGAGGCAGTAGGATCGCTTGAGCCCGGGAGGTCGAGGCTGCAGTGAGCCAGGACTGAG A G C11orf80 Ensembl:ENSG00000173715 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1443507328 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150981,RMVar_hsa_circ_119590,RMVar_hsa_circ_90981,RMVar_hsa_circ_150991 3764 RMVar_ID_3764 Human_SNP_ID_470410633 A-to-I Human chr11 + 66842128 66842128 66842128 CTGAAGCTGAGGCAGTAGGATCGCTTGAGCCCAGGAGGTCGAGGCTGCAGTGAGCCAGGACTGAG CTGAAGCTGAGGCAGTAGGATCGCTTGAGCCCTGGAGGTCGAGGCTGCAGTGAGCCAGGACTGAG A T C11orf80 Ensembl:ENSG00000173715 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1443507328 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_150981,RMVar_hsa_circ_119590,RMVar_hsa_circ_90981,RMVar_hsa_circ_150991 3765 RMVar_ID_3765 Human_SNP_ID_470415546 A-to-I Human chr11 - 66855150 66855150 66855150 CACAAAGGGGAGACTCAGTGGGGACCCTCCACATGACTCGGTGATGCAGAACGGTTATGACCTTC CACAAAGGGGAGACTCAGTGGGGACCCTCCACGTGACTCGGTGATGCAGAACGGTTATGACCTTC T C PC Ensembl:ENSG00000173599 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs911013676 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26776486 RMVar_hsa_circ_102572,RMVar_hsa_circ_112043,RMVar_hsa_circ_150997,RMVar_hsa_circ_150998 3766 RMVar_ID_3766 Human_SNP_ID_470427276 A-to-I Human chr11 - 66897326 66897326 66897326 CCTCAGGTAATCTGCCTGCTTCGGCCTCCCAAAGTGCTGGGATTATAGGTGTGAGCCACTGCACC CCTCAGGTAATCTGCCTGCTTCGGCCTCCCAAGGTGCTGGGATTATAGGTGTGAGCCACTGCACC T C PC Ensembl:ENSG00000173599 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1475572075 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_151009,RMVar_hsa_circ_80993 3767 RMVar_ID_3767 Human_SNP_ID_470439114 A-to-I Human chr11 - 66946444 66946444 66946444 TTGTATTTTTAGTAGAGACGGGGTTTCACCATATTGGCCAGGCTGATCTCGAACTCCCGACCTTG TTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGATCTCGAACTCCCGACCTTG T C PC Ensembl:ENSG00000173599 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1565304794 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6088252 RMVar_hsa_circ_151009,RMVar_hsa_circ_80993 3768 RMVar_ID_3768 Human_SNP_ID_470461579 A-to-I Human chr11 + 67035731 67035731 67035731 CGCCCGCCTTGGCCTCCCAAAGTACTGGGATTACAGACGTGAGCCACCGCGCCCGGCCCTTCCTT CGCCCGCCTTGGCCTCCCAAAGTACTGGGATTGCAGACGTGAGCCACCGCGCCCGGCCCTTCCTT A G SYT12 Ensembl:ENSG00000173227 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1259957953 Functional Loss SNV dbSNP153 33..33 33 - - - 3769 RMVar_ID_3769 Human_SNP_ID_470464518 A-to-I Human chr11 - 67045775 67045775 67045775 ACGGCTGTCTTCTTTTTGCTCATCTTCCTCCCATCCTGCAGCAGGTACACCTTGACGAAGGGGTC ACGGCTGTCTTCTTTTTGCTCATCTTCCTCCCGTCCTGCAGCAGGTACACCTTGACGAAGGGGTC T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1381490887 Functional Loss SNV dbSNP153 33..33 33 - - - 3770 RMVar_ID_3770 Human_SNP_ID_470471338 A-to-I Human chr11 + 67072075 67072075 67072075 GTTTTCTTTTTTTTGAGACGGAGTCTCGTTCTATCGCCCAGGCTGGAGTGCAGTGGCGCATTTCA GTTTTCTTTTTTTTGAGACGGAGTCTCGTTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCATTTCA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1316419066 Functional Loss SNV dbSNP153 33..33 33 - - - 3771 RMVar_ID_3771 Human_SNP_ID_470471956 A-to-I Human chr11 + 67074427 67074427 67074427 CAGTGGTTGCAGTGAGCTGAGAACACACCACTACCCTCCAGCCTGGATGACAGAGTGAGACTCTG CAGTGGTTGCAGTGAGCTGAGAACACACCACTGCCCTCCAGCCTGGATGACAGAGTGAGACTCTG A G lnc-KDM2A-4,lnc-KDM2A-4:2 RNACentral:URS00008B3D48,RNACentral:URS00008BE930 lincRNA,lincRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs778258229 Functional Loss SNV dbSNP153 33..33 33 - - - 3772 RMVar_ID_3772 Human_SNP_ID_470485937 A-to-I Human chr11 + 67125314 67125314 67125314 GTGATCTTCCCACGTCAGCTTCCCAGGTAGCTAGGACTACAGCCCTGTGCCACCATGCCTGGTTA GTGATCTTCCCACGTCAGCTTCCCAGGTAGCTGGGACTACAGCCCTGTGCCACCATGCCTGGTTA A G KDM2A Ensembl:ENSG00000173120 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1280099935 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11685274 RMVar_hsa_circ_151014,RMVar_hsa_circ_357875 3773 RMVar_ID_3773 Human_SNP_ID_470485939 A-to-I Human chr11 + 67125320 67125320 67125320 TTCCCACGTCAGCTTCCCAGGTAGCTAGGACTACAGCCCTGTGCCACCATGCCTGGTTAATTTTT TTCCCACGTCAGCTTCCCAGGTAGCTAGGACTGCAGCCCTGTGCCACCATGCCTGGTTAATTTTT A G KDM2A Ensembl:ENSG00000173120 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1352134128 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_151014,RMVar_hsa_circ_357875 3774 RMVar_ID_3774 Human_SNP_ID_470486044 A-to-I Human chr11 + 67125658 67125658 67125658 GCTGGGCACTGGGGGTGGTGGTGCGTGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGA GCTGGGCACTGGGGGTGGTGGTGCGTGCCTGTTATCCCAGCTACTTGGGAGGCTGAGGCAGGAGA A T KDM2A Ensembl:ENSG00000173120 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs987771368 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_151014,RMVar_hsa_circ_357875 3775 RMVar_ID_3775 Human_SNP_ID_470486209 A-to-I Human chr11 + 67126099 67126099 67126099 AGAAACCCCGTCTTTACTGAAAATACAAAATTAGCCGAACGTGGTGACGCATGCCTGTAATCCCA AGAAACCCCGTCTTTACTGAAAATACAAAATTGGCCGAACGTGGTGACGCATGCCTGTAATCCCA A G KDM2A Ensembl:ENSG00000173120 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1009292912 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11685283 RMVar_hsa_circ_151014,RMVar_hsa_circ_357875 3776 RMVar_ID_3776 Human_SNP_ID_470486345 A-to-I Human chr11 + 67126524 67126524 67126524 GAGGTCAGCAGTTTGAGACCAGCCTGACCAACAAGGTGGAACCCTGTCTCTACTAAAAATACAAA GAGGTCAGCAGTTTGAGACCAGCCTGACCAACGAGGTGGAACCCTGTCTCTACTAAAAATACAAA A G KDM2A Ensembl:ENSG00000173120 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs555637620 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_151014,RMVar_hsa_circ_357875 3777 RMVar_ID_3777 Human_SNP_ID_470486517 A-to-I Human chr11 + 67127146 67127146 67127146 TGGAGACAGGGTCTCACTCCGTTGCCCAGGCTAGAGTGCAGTGGTGTGATCATTCCTCTTTGTAG TGGAGACAGGGTCTCACTCCGTTGCCCAGGCTGGAGTGCAGTGGTGTGATCATTCCTCTTTGTAG A G KDM2A Ensembl:ENSG00000173120 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1035862216 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11685298 RMVar_hsa_circ_151014,RMVar_hsa_circ_357875 3778 RMVar_ID_3778 Human_SNP_ID_470487417 A-to-I Human chr11 + 67130345 67130345 67130345 TTATATTGTTTTAGTAGAGACAGGGTTTCACCATGTTGGTCAGGCTGGTCTCAAACTCCTCACCT TTATATTGTTTTAGTAGAGACAGGGTTTCACCGTGTTGGTCAGGCTGGTCTCAAACTCCTCACCT A G KDM2A Ensembl:ENSG00000173120 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs887502043 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_151014,RMVar_hsa_circ_357875 3779 RMVar_ID_3779 Human_SNP_ID_470487428 A-to-I Human chr11 + 67130405 67130404 67130406 CACCTCCAGTGATCCGCCCACTTCGGCCTCCCAAAGTGTTGGGATTACAGGCGTGAGCCACCATG CACCTCCAGTGATCCGCCCACTTCGGCCTCCC__AGTGTTGGGATTACAGGCGTGAGCCACCATG CAA C KDM2A Ensembl:ENSG00000173120 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1397997237 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_151014,RMVar_hsa_circ_357875 3780 RMVar_ID_3780 Human_SNP_ID_470488908 A-to-I Human chr11 + 67135940 67135940 67135940 TACTGAAGTCTAGATTCTAGATAGCTCATCCTATCATATACTTTCATTGCATTCTGTGTTTACCT TACTGAAGTCTAGATTCTAGATAGCTCATCCTGTCATATACTTTCATTGCATTCTGTGTTTACCT A G KDM2A Ensembl:ENSG00000173120 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs538697420 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4595,RMVar_hsa_circ_72699,RMVar_hsa_circ_151014,RMVar_hsa_circ_357875,RMVar_hsa_circ_330836,RMVar_hsa_circ_41037,RMVar_hsa_circ_53993,RMVar_hsa_circ_23665 3781 RMVar_ID_3781 Human_SNP_ID_470488913 A-to-I Human chr11 + 67135945 67135945 67135945 AAGTCTAGATTCTAGATAGCTCATCCTATCATATACTTTCATTGCATTCTGTGTTTACCTTTGTT AAGTCTAGATTCTAGATAGCTCATCCTATCATGTACTTTCATTGCATTCTGTGTTTACCTTTGTT A G KDM2A Ensembl:ENSG00000173120 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1161518467 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4595,RMVar_hsa_circ_72699,RMVar_hsa_circ_151014,RMVar_hsa_circ_357875,RMVar_hsa_circ_330836,RMVar_hsa_circ_41037,RMVar_hsa_circ_53993,RMVar_hsa_circ_23665 3782 RMVar_ID_3782 Human_SNP_ID_470488922 A-to-I Human chr11 + 67135992 67135992 67135992 TCTGTGTTTACCTTTGTTGCCTTTGTGTAACTATAATTAACGTTACTAGTGTGTTTGTTTAATAT TCTGTGTTTACCTTTGTTGCCTTTGTGTAACTGTAATTAACGTTACTAGTGTGTTTGTTTAATAT A G KDM2A Ensembl:ENSG00000173120 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1018318379 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4595,RMVar_hsa_circ_72699,RMVar_hsa_circ_151014,RMVar_hsa_circ_357875,RMVar_hsa_circ_330836,RMVar_hsa_circ_41037,RMVar_hsa_circ_53993,RMVar_hsa_circ_23665 3783 RMVar_ID_3783 Human_SNP_ID_470489107 A-to-I Human chr11 + 67136945 67136945 67136945 CACAAAGGGCTACAAAGGTAAACATAGGCTGCAGTAACAGTATATGATAGAGTGAGCTAATCTAG CACAAAGGGCTACAAAGGTAAACATAGGCTGCTGTAACAGTATATGATAGAGTGAGCTAATCTAG A T KDM2A Ensembl:ENSG00000173120 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1026660023 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4595,RMVar_hsa_circ_72699,RMVar_hsa_circ_151014,RMVar_hsa_circ_357875,RMVar_hsa_circ_330836,RMVar_hsa_circ_41037,RMVar_hsa_circ_53993,RMVar_hsa_circ_23665 3784 RMVar_ID_3784 Human_SNP_ID_470489516 A-to-I Human chr11 + 67138638 67138638 67138638 TCCCATGTCTACCAAAAACACAAAAATTAACCAGGTGTGGTGGTGTGCACCTGTAATCCAACCTA TCCCATGTCTACCAAAAACACAAAAATTAACCGGGTGTGGTGGTGTGCACCTGTAATCCAACCTA A G KDM2A Ensembl:ENSG00000173120 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs912095536 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4595,RMVar_hsa_circ_72699,RMVar_hsa_circ_151014,RMVar_hsa_circ_357875,RMVar_hsa_circ_330836,RMVar_hsa_circ_41037,RMVar_hsa_circ_53993,RMVar_hsa_circ_23665 3785 RMVar_ID_3785 Human_SNP_ID_470489524 A-to-I Human chr11 + 67138660 67138660 67138660 AAAATTAACCAGGTGTGGTGGTGTGCACCTGTAATCCAACCTACTAGGGAAGCTGAGGCAGAAGA AAAATTAACCAGGTGTGGTGGTGTGCACCTGTCATCCAACCTACTAGGGAAGCTGAGGCAGAAGA A C KDM2A Ensembl:ENSG00000173120 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs922074740 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4595,RMVar_hsa_circ_72699,RMVar_hsa_circ_151014,RMVar_hsa_circ_357875,RMVar_hsa_circ_330836,RMVar_hsa_circ_41037,RMVar_hsa_circ_53993,RMVar_hsa_circ_23665 3786 RMVar_ID_3786 Human_SNP_ID_470489527 A-to-I Human chr11 + 67138670 67138670 67138670 AGGTGTGGTGGTGTGCACCTGTAATCCAACCTACTAGGGAAGCTGAGGCAGAAGAATTGCTTGAA AGGTGTGGTGGTGTGCACCTGTAATCCAACCTTCTAGGGAAGCTGAGGCAGAAGAATTGCTTGAA A T KDM2A Ensembl:ENSG00000173120 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs528006466 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4595,RMVar_hsa_circ_72699,RMVar_hsa_circ_151014,RMVar_hsa_circ_357875,RMVar_hsa_circ_330836,RMVar_hsa_circ_41037,RMVar_hsa_circ_53993,RMVar_hsa_circ_23665 3787 RMVar_ID_3787 Human_SNP_ID_470489909 A-to-I Human chr11 + 67140103 67140103 67140103 GGTTTGTGGATTGGGTACGGTGGCTTACACCTATAATCCCAACACTTTGGGAGGCTAAGGCAGGA GGTTTGTGGATTGGGTACGGTGGCTTACACCTGTAATCCCAACACTTTGGGAGGCTAAGGCAGGA A G KDM2A Ensembl:ENSG00000173120 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs141456221 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17560024,Human_RBP_ID_24898973 RMVar_hsa_circ_4595,RMVar_hsa_circ_72699,RMVar_hsa_circ_151014,RMVar_hsa_circ_357875,RMVar_hsa_circ_330836,RMVar_hsa_circ_41037,RMVar_hsa_circ_53993,RMVar_hsa_circ_23665 3788 RMVar_ID_3788 Human_SNP_ID_470490660 A-to-I Human chr11 + 67142686 67142686 67142686 AGATTGCACCATCGCACTCCAGACTGGGGGACAAGCGTGAGACTCCATCTCAAAAAAAAAAGTTA AGATTGCACCATCGCACTCCAGACTGGGGGACGAGCGTGAGACTCCATCTCAAAAAAAAAAGTTA A G KDM2A Ensembl:ENSG00000173120 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1193003336 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4595,RMVar_hsa_circ_72699,RMVar_hsa_circ_151014,RMVar_hsa_circ_357875,RMVar_hsa_circ_330836,RMVar_hsa_circ_41037,RMVar_hsa_circ_53993,RMVar_hsa_circ_23665 3789 RMVar_ID_3789 Human_SNP_ID_470491722 A-to-I Human chr11 + 67146540 67146540 67146540 GTCTTCCTTTTTATTGTTTGAGACAGGGTCTCACTTTGTTATCCACGCTGGAGTGCAGTGGCATA GTCTTCCTTTTTATTGTTTGAGACAGGGTCTCGCTTTGTTATCCACGCTGGAGTGCAGTGGCATA A G KDM2A Ensembl:ENSG00000173120 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1262269145 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4595,RMVar_hsa_circ_72699,RMVar_hsa_circ_151014,RMVar_hsa_circ_357875,RMVar_hsa_circ_330836,RMVar_hsa_circ_41037,RMVar_hsa_circ_53993,RMVar_hsa_circ_23665 3790 RMVar_ID_3790 Human_SNP_ID_470491729 A-to-I Human chr11 + 67146572 67146572 67146572 ACTTTGTTATCCACGCTGGAGTGCAGTGGCATAATCTAGGTTCACTGCAACCTCCACCTCCCAGA ACTTTGTTATCCACGCTGGAGTGCAGTGGCATGATCTAGGTTCACTGCAACCTCCACCTCCCAGA A G KDM2A Ensembl:ENSG00000173120 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs138370035 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4595,RMVar_hsa_circ_72699,RMVar_hsa_circ_151014,RMVar_hsa_circ_357875,RMVar_hsa_circ_330836,RMVar_hsa_circ_41037,RMVar_hsa_circ_53993,RMVar_hsa_circ_23665 3791 RMVar_ID_3791 Human_SNP_ID_470492075 A-to-I Human chr11 + 67147862 67147862 67147862 ACCACACCCAGCTAATTTTTTGTATTTTTAGTAGAGACGAGGTTTTACCATGTTGGCCAGGCTGT ACCACACCCAGCTAATTTTTTGTATTTTTAGTTGAGACGAGGTTTTACCATGTTGGCCAGGCTGT A T KDM2A Ensembl:ENSG00000173120 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs994201990 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4595,RMVar_hsa_circ_72699,RMVar_hsa_circ_151014,RMVar_hsa_circ_357875,RMVar_hsa_circ_330836,RMVar_hsa_circ_41037,RMVar_hsa_circ_53993,RMVar_hsa_circ_23665 3792 RMVar_ID_3792 Human_SNP_ID_470492638 A-to-I Human chr11 + 67149814 67149814 67149814 ACGATCTCGGCTCACTGCAACCTCGGCCTCCCAGGTTCAAGTGATTCTCCTGCCTCAGCCACCCA ACGATCTCGGCTCACTGCAACCTCGGCCTCCCGGGTTCAAGTGATTCTCCTGCCTCAGCCACCCA A G KDM2A Ensembl:ENSG00000173120 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs532916385 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4595,RMVar_hsa_circ_72699,RMVar_hsa_circ_151014,RMVar_hsa_circ_357875,RMVar_hsa_circ_330836,RMVar_hsa_circ_41037,RMVar_hsa_circ_53993,RMVar_hsa_circ_23665 3793 RMVar_ID_3793 Human_SNP_ID_470493149 A-to-I Human chr11 + 67151878 67151878 67151878 GCAATTCTCTTACCTCAACCTCCTGCGTAGCTAGGACTATAGGCATGTACCACCACACCGGGCTA GCAATTCTCTTACCTCAACCTCCTGCGTAGCTGGGACTATAGGCATGTACCACCACACCGGGCTA A G KDM2A Ensembl:ENSG00000173120 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1230715801 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4595,RMVar_hsa_circ_72699,RMVar_hsa_circ_151014,RMVar_hsa_circ_357875,RMVar_hsa_circ_330836,RMVar_hsa_circ_41037,RMVar_hsa_circ_53993,RMVar_hsa_circ_23665 3794 RMVar_ID_3794 Human_SNP_ID_470493150 A-to-I Human chr11 + 67151884 67151884 67151884 CTCTTACCTCAACCTCCTGCGTAGCTAGGACTATAGGCATGTACCACCACACCGGGCTAATTTTT CTCTTACCTCAACCTCCTGCGTAGCTAGGACTGTAGGCATGTACCACCACACCGGGCTAATTTTT A G KDM2A Ensembl:ENSG00000173120 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1295095663 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4595,RMVar_hsa_circ_72699,RMVar_hsa_circ_151014,RMVar_hsa_circ_357875,RMVar_hsa_circ_330836,RMVar_hsa_circ_41037,RMVar_hsa_circ_53993,RMVar_hsa_circ_23665 3795 RMVar_ID_3795 Human_SNP_ID_470504058 A-to-I Human chr11 + 67193805 67193805 67193805 ACTGCTTGAACCCAGGAGCGGGAGGTTGCGGTAAGCTGAGACCATGTCGTTGTATTCCAGCCTGG ACTGCTTGAACCCAGGAGCGGGAGGTTGCGGTGAGCTGAGACCATGTCGTTGTATTCCAGCCTGG A G KDM2A Ensembl:ENSG00000173120 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1221467937 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17560389 RMVar_hsa_circ_4595,RMVar_hsa_circ_72699,RMVar_hsa_circ_151014,RMVar_hsa_circ_357875,RMVar_hsa_circ_330836,RMVar_hsa_circ_41037,RMVar_hsa_circ_5092,RMVar_hsa_circ_151016,RMVar_hsa_circ_80926,RMVar_hsa_circ_285346,RMVar_hsa_circ_354083,RMVar_hsa_circ_366144,RMVar_hsa_circ_120484,RMVar_hsa_circ_151018,RMVar_hsa_circ_73265,RMVar_hsa_circ_151019,RMVar_hsa_circ_151017,RMVar_hsa_circ_5185,RMVar_hsa_circ_151020,RMVar_hsa_circ_323960 3796 RMVar_ID_3796 Human_SNP_ID_470508582 A-to-I Human chr11 + 67209917 67209917 67209917 ACCTCATCTCTACAAAATTTGGAAACTTAGCCAGGCATGGTGGCATGCACCTGTAGTCCTGGTTA ACCTCATCTCTACAAAATTTGGAAACTTAGCCGGGCATGGTGGCATGCACCTGTAGTCCTGGTTA A G KDM2A Ensembl:ENSG00000173120 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1176962143 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4595,RMVar_hsa_circ_72699,RMVar_hsa_circ_41037,RMVar_hsa_circ_151022,RMVar_hsa_circ_5092,RMVar_hsa_circ_80926,RMVar_hsa_circ_354083,RMVar_hsa_circ_366144,RMVar_hsa_circ_120484,RMVar_hsa_circ_151018,RMVar_hsa_circ_73265,RMVar_hsa_circ_151019,RMVar_hsa_circ_151017,RMVar_hsa_circ_101433,RMVar_hsa_circ_292078,RMVar_hsa_circ_151020,RMVar_hsa_circ_323960,RMVar_hsa_circ_340047,RMVar_hsa_circ_341800,RMVar_hsa_circ_293178,RMVar_hsa_circ_284707,RMVar_hsa_circ_265098,RMVar_hsa_circ_151024,RMVar_hsa_circ_151025,RMVar_hsa_circ_151023,RMVar_hsa_circ_151021 3797 RMVar_ID_3797 Human_SNP_ID_470508590 A-to-I Human chr11 + 67209953 67209953 67209953 ATGGTGGCATGCACCTGTAGTCCTGGTTACTCAAGAGACCGAGGTGGGAGGATTGCTTGAGCCTG ATGGTGGCATGCACCTGTAGTCCTGGTTACTCGAGAGACCGAGGTGGGAGGATTGCTTGAGCCTG A G KDM2A Ensembl:ENSG00000173120 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1257070311 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4595,RMVar_hsa_circ_72699,RMVar_hsa_circ_41037,RMVar_hsa_circ_151022,RMVar_hsa_circ_5092,RMVar_hsa_circ_80926,RMVar_hsa_circ_354083,RMVar_hsa_circ_366144,RMVar_hsa_circ_120484,RMVar_hsa_circ_151018,RMVar_hsa_circ_73265,RMVar_hsa_circ_151019,RMVar_hsa_circ_151017,RMVar_hsa_circ_101433,RMVar_hsa_circ_292078,RMVar_hsa_circ_151020,RMVar_hsa_circ_323960,RMVar_hsa_circ_340047,RMVar_hsa_circ_341800,RMVar_hsa_circ_293178,RMVar_hsa_circ_284707,RMVar_hsa_circ_265098,RMVar_hsa_circ_151024,RMVar_hsa_circ_151025,RMVar_hsa_circ_151023,RMVar_hsa_circ_151021 3798 RMVar_ID_3798 Human_SNP_ID_470508603 A-to-I Human chr11 + 67210025 67210025 67210025 GAGGCTGCAGTGAGCTGTGATCACTGTAGCCTAGCCAACATTGCAAGAATCTGTCTCAAAAAAAT GAGGCTGCAGTGAGCTGTGATCACTGTAGCCTGGCCAACATTGCAAGAATCTGTCTCAAAAAAAT A G KDM2A Ensembl:ENSG00000173120 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1041871084 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4595,RMVar_hsa_circ_72699,RMVar_hsa_circ_41037,RMVar_hsa_circ_151022,RMVar_hsa_circ_5092,RMVar_hsa_circ_80926,RMVar_hsa_circ_354083,RMVar_hsa_circ_366144,RMVar_hsa_circ_120484,RMVar_hsa_circ_151018,RMVar_hsa_circ_73265,RMVar_hsa_circ_151019,RMVar_hsa_circ_151017,RMVar_hsa_circ_101433,RMVar_hsa_circ_292078,RMVar_hsa_circ_151020,RMVar_hsa_circ_323960,RMVar_hsa_circ_340047,RMVar_hsa_circ_341800,RMVar_hsa_circ_293178,RMVar_hsa_circ_284707,RMVar_hsa_circ_265098,RMVar_hsa_circ_151024,RMVar_hsa_circ_151025,RMVar_hsa_circ_151023,RMVar_hsa_circ_151021 3799 RMVar_ID_3799 Human_SNP_ID_470508896 A-to-I Human chr11 + 67211345 67211345 67211345 AGTCAAAATATAGAAAATAAGCCAGGTGCGGTAGCTCACGCCTACAATCCCAGCACTCTGGGAGG AGTCAAAATATAGAAAATAAGCCAGGTGCGGTGGCTCACGCCTACAATCCCAGCACTCTGGGAGG A G KDM2A Ensembl:ENSG00000173120 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs528837756 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4595,RMVar_hsa_circ_72699,RMVar_hsa_circ_41037,RMVar_hsa_circ_151022,RMVar_hsa_circ_5092,RMVar_hsa_circ_80926,RMVar_hsa_circ_354083,RMVar_hsa_circ_366144,RMVar_hsa_circ_120484,RMVar_hsa_circ_151018,RMVar_hsa_circ_73265,RMVar_hsa_circ_151019,RMVar_hsa_circ_151017,RMVar_hsa_circ_101433,RMVar_hsa_circ_292078,RMVar_hsa_circ_151020,RMVar_hsa_circ_323960,RMVar_hsa_circ_340047,RMVar_hsa_circ_341800,RMVar_hsa_circ_293178,RMVar_hsa_circ_284707,RMVar_hsa_circ_265098,RMVar_hsa_circ_151024,RMVar_hsa_circ_151025,RMVar_hsa_circ_151023,RMVar_hsa_circ_151021 3800 RMVar_ID_3800 Human_SNP_ID_470513280 A-to-I Human chr11 + 67228860 67228860 67228860 CTGGGCTCAAGCAATCCCCCTCCTGAGTAACTAGGATTACAAGCACACACCACTATGCCCAGCTA CTGGGCTCAAGCAATCCCCCTCCTGAGTAACTCGGATTACAAGCACACACCACTATGCCCAGCTA A C KDM2A Ensembl:ENSG00000173120 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs577771609 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72699,RMVar_hsa_circ_354083,RMVar_hsa_circ_284707,RMVar_hsa_circ_265098,RMVar_hsa_circ_49948,RMVar_hsa_circ_115497,RMVar_hsa_circ_151030,RMVar_hsa_circ_296943,RMVar_hsa_circ_364268,RMVar_hsa_circ_151021,RMVar_hsa_circ_91208,RMVar_hsa_circ_367294,RMVar_hsa_circ_151031,RMVar_hsa_circ_295185,RMVar_hsa_circ_151034 3801 RMVar_ID_3801 Human_SNP_ID_470513281 A-to-I Human chr11 + 67228860 67228860 67228860 CTGGGCTCAAGCAATCCCCCTCCTGAGTAACTAGGATTACAAGCACACACCACTATGCCCAGCTA CTGGGCTCAAGCAATCCCCCTCCTGAGTAACTGGGATTACAAGCACACACCACTATGCCCAGCTA A G KDM2A Ensembl:ENSG00000173120 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs577771609 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72699,RMVar_hsa_circ_354083,RMVar_hsa_circ_284707,RMVar_hsa_circ_265098,RMVar_hsa_circ_49948,RMVar_hsa_circ_115497,RMVar_hsa_circ_151030,RMVar_hsa_circ_296943,RMVar_hsa_circ_364268,RMVar_hsa_circ_151021,RMVar_hsa_circ_91208,RMVar_hsa_circ_367294,RMVar_hsa_circ_151031,RMVar_hsa_circ_295185,RMVar_hsa_circ_151034 3802 RMVar_ID_3802 Human_SNP_ID_470513802 A-to-I Human chr11 + 67231015 67231015 67231015 GTCTCACTCTCTTGCCCAGGCTGGAGTGCAGTAATATGATCGCAGCTCACTGCAGCCTCAACCTC GTCTCACTCTCTTGCCCAGGCTGGAGTGCAGTCATATGATCGCAGCTCACTGCAGCCTCAACCTC A C KDM2A Ensembl:ENSG00000173120 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs989963420 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1126190 RMVar_hsa_circ_72699,RMVar_hsa_circ_354083,RMVar_hsa_circ_284707,RMVar_hsa_circ_265098,RMVar_hsa_circ_49948,RMVar_hsa_circ_115497,RMVar_hsa_circ_151030,RMVar_hsa_circ_296943,RMVar_hsa_circ_364268,RMVar_hsa_circ_151021,RMVar_hsa_circ_91208,RMVar_hsa_circ_367294,RMVar_hsa_circ_151031,RMVar_hsa_circ_295185,RMVar_hsa_circ_151034 3803 RMVar_ID_3803 Human_SNP_ID_470514719 A-to-I Human chr11 + 67234690 67234690 67234690 CAGCCTGGGCAACGTGGCGAAACCTCACCTCCACAAAAATACAAAATTATCCAGGTGTGGTGGTG CAGCCTGGGCAACGTGGCGAAACCTCACCTCCCCAAAAATACAAAATTATCCAGGTGTGGTGGTG A C KDM2A Ensembl:ENSG00000173120 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1258998311 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72699,RMVar_hsa_circ_265098,RMVar_hsa_circ_115497,RMVar_hsa_circ_151030,RMVar_hsa_circ_364268,RMVar_hsa_circ_91208,RMVar_hsa_circ_367294,RMVar_hsa_circ_151031,RMVar_hsa_circ_151034 3804 RMVar_ID_3804 Human_SNP_ID_470531125 A-to-I Human chr11 + 67293792 67293792 67293792 TGCCTACCTGGGCCTCCCACAGTGCTGGGATTACAGGCATGAGCCACCACACCTATCCCTTCACC TGCCTACCTGGGCCTCCCACAGTGCTGGGATTGCAGGCATGAGCCACCACACCTATCCCTTCACC A G ANKRD13D Ensembl:ENSG00000172932 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1250741294 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_151040,RMVar_hsa_circ_82821 3805 RMVar_ID_3805 Human_SNP_ID_470531932 A-to-I Human chr11 + 67297241 67297237 67297241 GCATGTCTTTTCTTTTTTTGACATGGGGTCTCACTCCATCGCCCAGGCTGGAGTGCAGTGGTGTG GCATGTCTTTTCTTTTTTTGACATGGGGT____CTCCATCGCCCAGGCTGGAGTGCAGTGGTGTG TCTCA T ANKRD13D Ensembl:ENSG00000172932 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1325837955 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_750387,Human_RBP_ID_11760055 RMVar_hsa_circ_151040,RMVar_hsa_circ_82821 3806 RMVar_ID_3806 Human_SNP_ID_470536225 A-to-I Human chr11 + 67310227 67310227 67310227 AGGCATGGAAGAGAGCCAGGCAGCCCCGAAAGAAGAGCCTGGGCCACGGCCACGTATAAACCTCC AGGCATGGAAGAGAGCCAGGCAGCCCCGAAAGGAGAGCCTGGGCCACGGCCACGTATAAACCTCC A G SSH3 Ensembl:ENSG00000172830 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs750166856 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18972383 Human_Splice_Rec_1265824 3807 RMVar_ID_3807 Human_SNP_ID_470543533 A-to-I Human chr11 + 67340342 67340342 67340342 TAAAACTAGGCTGGGTACCATGGCATATGACTATAGTCCCAGCACTTTGGGAGGCTGAGGCAGGA TAAAACTAGGCTGGGTACCATGGCATATGACTGTAGTCCCAGCACTTTGGGAGGCTGAGGCAGGA A G RAD9A Ensembl:ENSG00000172613 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs774323515 Functional Loss SNV dbSNP153 33..33 33 - - - 3808 RMVar_ID_3808 Human_SNP_ID_470544337 A-to-I Human chr11 + 67343978 67343977 67343978 GTGGGCTAATTTTTAACAGTTTTTGTAGAGACAAGATTTTGCTATGTTACCTGGGCTGGACTTGA GTGGGCTAATTTTTAACAGTTTTTGTAGAGAC_AGATTTTGCTATGTTACCTGGGCTGGACTTGA CA C RAD9A Ensembl:ENSG00000172613 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs925458544 Functional Loss DEL dbSNP153 33..33 33 - - - 3809 RMVar_ID_3809 Human_SNP_ID_470544341 A-to-I Human chr11 + 67343989 67343987 67343989 TTTAACAGTTTTTGTAGAGACAAGATTTTGCTATGTTACCTGGGCTGGACTTGAACCCTTGGCCT TTTAACAGTTTTTGTAGAGACAAGATTTTGC__TGTTACCTGGGCTGGACTTGAACCCTTGGCCT CTA C RAD9A Ensembl:ENSG00000172613 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1291359162 Functional Loss DEL dbSNP153 32..33 33 - - - 3810 RMVar_ID_3810 Human_SNP_ID_470544342 A-to-I Human chr11 + 67343989 67343989 67343989 TTTAACAGTTTTTGTAGAGACAAGATTTTGCTATGTTACCTGGGCTGGACTTGAACCCTTGGCCT TTTAACAGTTTTTGTAGAGACAAGATTTTGCTGTGTTACCTGGGCTGGACTTGAACCCTTGGCCT A G RAD9A Ensembl:ENSG00000172613 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs556372455 Functional Loss SNV dbSNP153 33..33 33 - - - 3811 RMVar_ID_3811 Human_SNP_ID_470545936 A-to-I Human chr11 + 67350848 67350848 67350848 TCACCCAGGCTGGAGTGCAGTGATGCGGTCTCAGCTCACTGCCAGCTCTGCCTCCCGGGTTCACG TCACCCAGGCTGGAGTGCAGTGATGCGGTCTCGGCTCACTGCCAGCTCTGCCTCCCGGGTTCACG A G RAD9A Ensembl:ENSG00000172613 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1374939086 Functional Loss SNV dbSNP153 33..33 33 - - - 3812 RMVar_ID_3812 Human_SNP_ID_470548107 A-to-I Human chr11 + 67359798 67359798 67359798 GAACTCCTGGGCTCAAGTGAGCCTCCTGCCTCAGCTTCCCAAAGTGCTGGGATTATAGGTGTGCG GAACTCCTGGGCTCAAGTGAGCCTCCTGCCTCTGCTTCCCAAAGTGCTGGGATTATAGGTGTGCG A T RAD9A Ensembl:ENSG00000172613 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs930998596 Functional Loss SNV dbSNP153 33..33 33 - - - 3813 RMVar_ID_3813 Human_SNP_ID_470560404 A-to-I Human chr11 - 67402989 67402989 67402989 AGTCTCGCACTGTCGCCTGGGCTCCACTTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCA AGTCTCGCACTGTCGCCTGGGCTCCACTTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCA T C PPP1CA Ensembl:ENSG00000172531 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1252055651 Functional Loss SNV dbSNP153 33..33 33 - - - 3814 RMVar_ID_3814 Human_SNP_ID_470573462 A-to-I Human chr11 - 67441806 67441806 67441806 CTGACCTCCCCGCTGACAGAGCCGGTGGTGGTACTGGAGGGGCACACCAAGCGAGTGGGCATCAT CTGACCTCCCCGCTGACAGAGCCGGTGGTGGTGCTGGAGGGGCACACCAAGCGAGTGGGCATCAT T C CORO1B Ensembl:ENSG00000172725 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs770607931 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_867927,Human_RBP_ID_4186107,Human_RBP_ID_18188326,Human_RBP_ID_22433143 Human_Splice_Rec_1266468,Human_Splice_Rec_1266469,Human_Splice_Rec_1266488,Human_Splice_Rec_1266489,Human_Splice_Rec_1266510,Human_Splice_Rec_1266511,Human_Splice_Rec_1266530,Human_Splice_Rec_1266531,Human_Splice_Rec_1266560,Human_Splice_Rec_1266561,Human_Splice_Rec_1266572,Human_Splice_Rec_1266573,Human_Splice_Rec_1266582,Human_Splice_Rec_1266590 3815 RMVar_ID_3815 Human_SNP_ID_470576829 A-to-I Human chr11 + 67453086 67453086 67453086 GCCCAGGATGAGTGCAGTGGCACAGTCCCTGCAGCTTCCACCTCCTGGGTTCCAGCGACCCTCCC GCCCAGGATGAGTGCAGTGGCACAGTCCCTGCCGCTTCCACCTCCTGGGTTCCAGCGACCCTCCC A C CABP4 Ensembl:ENSG00000175544 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1413760204 Functional Loss SNV dbSNP153 33..33 33 - - - 3816 RMVar_ID_3816 Human_SNP_ID_470576830 A-to-I Human chr11 + 67453093 67453093 67453093 ATGAGTGCAGTGGCACAGTCCCTGCAGCTTCCACCTCCTGGGTTCCAGCGACCCTCCCATCTCAG ATGAGTGCAGTGGCACAGTCCCTGCAGCTTCCTCCTCCTGGGTTCCAGCGACCCTCCCATCTCAG A T CABP4 Ensembl:ENSG00000175544 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs986847355 Functional Loss SNV dbSNP153 33..33 33 - - - 3817 RMVar_ID_3817 Human_SNP_ID_470576864 A-to-I Human chr11 + 67453232 67453231 67453233 GTTGCCCAGGCTGGTCTTGAACTCGTGAGCTCAAGTGATCCTCCTACCTTGGCCTCCTGAAATGT GTTGCCCAGGCTGGTCTTGAACTCGTGAGCTC__GTGATCCTCCTACCTTGGCCTCCTGAAATGT CAA C CABP4 Ensembl:ENSG00000175544 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1565158525 Functional Loss DEL dbSNP153 33..34 33 - - - 3818 RMVar_ID_3818 Human_SNP_ID_470576941 A-to-I Human chr11 + 67453593 67453593 67453593 CTACTCAGGAGAATCGCTTGAACCCGGGAGGCAGAGGTTGTGGTGAGCCAAGATCGTGCCATCGC CTACTCAGGAGAATCGCTTGAACCCGGGAGGCTGAGGTTGTGGTGAGCCAAGATCGTGCCATCGC A T CABP4 Ensembl:ENSG00000175544 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1454449178 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1266608 3819 RMVar_ID_3819 Human_SNP_ID_470612702 A-to-I Human chr11 + 67584548 67584548 67584548 GGAGGAGGTGGTGACCGTGGAGACGTGGCAGGAGGGCTCACTCAAAGCCTCCTGCGTAAGTGACC GGAGGAGGTGGTGACCGTGGAGACGTGGCAGGGGGGCTCACTCAAAGCCTCCTGCGTAAGTGACC A G GSTP1 Ensembl:ENSG00000084207 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs769620801 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226120,Human_RBP_ID_749000,Human_RBP_ID_4185197,Human_RBP_ID_5313749,Human_RBP_ID_17648459,Human_RBP_ID_17800077,Human_RBP_ID_22435505 Human_Splice_Rec_1267044,Human_Splice_Rec_1267045,Human_Splice_Rec_1267054,Human_Splice_Rec_1267055,Human_Splice_Rec_1267078,Human_Splice_Rec_1267079,Human_Splice_Rec_1267081 RMVar_hsa_circ_103121,RMVar_hsa_circ_109001,RMVar_hsa_circ_125578,RMVar_hsa_circ_151079,RMVar_hsa_circ_124211,RMVar_hsa_circ_151081,RMVar_hsa_circ_93515,RMVar_hsa_circ_151082,RMVar_hsa_circ_151080,RMVar_hsa_circ_318490,RMVar_hsa_circ_151084,RMVar_hsa_circ_114794,RMVar_hsa_circ_151085,RMVar_hsa_circ_151083 3820 RMVar_ID_3820 Human_SNP_ID_470641151 A-to-I Human chr11 - 67682754 67682754 67682754 TGCAGCATCCAGTTCATCTTAAGAATGTCAACAATTAGTCATGCAATAAATGTTCTGGTTTTAAA TGCAGCATCCAGTTCATCTTAAGAATGTCAACGATTAGTCATGCAATAAATGTTCTGGTTTTAAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879110440 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26410684 3821 RMVar_ID_3821 Human_SNP_ID_470641218 A-to-I Human chr11 - 67683014 67683014 67683014 GCATCATCGTTTGGAAAGCATCGCAATAAGACACACACGTTGTGCCGCTGCTGTGGCTCTGAGGC GCATCATCGTTTGGAAAGCATCGCAATAAGACGCACACGTTGTGCCGCTGCTGTGGCTCTGAGGC T C RPL37P2 Ensembl:ENSG00000239559 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs889169888 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1884531 3822 RMVar_ID_3822 Human_SNP_ID_470641224 A-to-I Human chr11 - 67683027 67683027 67683027 GATGACGAAGGGAGCATCATCGTTTGGAAAGCATCGCAATAAGACACACACGTTGTGCCGCTGCT GATGACGAAGGGAGCATCATCGTTTGGAAAGCGTCGCAATAAGACACACACGTTGTGCCGCTGCT T C RPL37P2 Ensembl:ENSG00000239559 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388729069 Functional Loss SNV dbSNP153 33..33 33 - - - 3823 RMVar_ID_3823 Human_SNP_ID_470641228 A-to-I Human chr11 - 67683044 67683044 67683044 CTCGGCCGCAGAAGCGAGATGACGAAGGGAGCATCATCGTTTGGAAAGCATCGCAATAAGACACA CTCGGCCGCAGAAGCGAGATGACGAAGGGAGCGTCATCGTTTGGAAAGCATCGCAATAAGACACA T C RPL37P2 Ensembl:ENSG00000239559 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs999102448 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22893526,Human_RBP_ID_26410685 3824 RMVar_ID_3824 Human_SNP_ID_470752276 A-to-I Human chr11 + 68031568 68031568 68031568 CGGGGTTCCACCATGTTAGCCAGGCTGGTCTCAAACTCCTGACCTCAGGTGATCCACCTGCCTCA CGGGGTTCCACCATGTTAGCCAGGCTGGTCTCCAACTCCTGACCTCAGGTGATCCACCTGCCTCA A C NDUFS8 Ensembl:ENSG00000110717 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs928046993 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1267870 RMVar_hsa_circ_79704,RMVar_hsa_circ_151101 3825 RMVar_ID_3825 Human_SNP_ID_470760513 A-to-I Human chr11 - 68055788 68055788 68055788 CACCCGCCTTGGCCTCCCAAAGTGCTAGGATTACAGGCATGAGCCACCGCGCCCGGCCTCAGCCT CACCCGCCTTGGCCTCCCAAAGTGCTAGGATTGCAGGCATGAGCCACCGCGCCCGGCCTCAGCCT T C CHKA Ensembl:ENSG00000110721 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1299561940 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5166701 RMVar_hsa_circ_77068,RMVar_hsa_circ_111004,RMVar_hsa_circ_98826,RMVar_hsa_circ_151129,RMVar_hsa_circ_151130,RMVar_hsa_circ_151131 3826 RMVar_ID_3826 Human_SNP_ID_470760934 A-to-I Human chr11 - 68057458 68057458 68057458 AAAATTAGCCGGGCCTGGTGGCAGGTGCCTGTAGTCCCAGCTACTGGAGAGGCTGAGGCAGGAGA AAAATTAGCCGGGCCTGGTGGCAGGTGCCTGTCGTCCCAGCTACTGGAGAGGCTGAGGCAGGAGA T G CHKA Ensembl:ENSG00000110721 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs946257944 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77068,RMVar_hsa_circ_111004,RMVar_hsa_circ_98826,RMVar_hsa_circ_151129,RMVar_hsa_circ_151130,RMVar_hsa_circ_151131 3827 RMVar_ID_3827 Human_SNP_ID_470761134 A-to-I Human chr11 - 68058171 68058171 68058171 AGTAATGTAAATCATCCAGGTGTGGTGGCTCAAGCCAGTCATCCAGCACTTTGGGAGGCTGAGGC AGTAATGTAAATCATCCAGGTGTGGTGGCTCAGGCCAGTCATCCAGCACTTTGGGAGGCTGAGGC T C CHKA Ensembl:ENSG00000110721 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1414529331 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77068,RMVar_hsa_circ_111004,RMVar_hsa_circ_98826,RMVar_hsa_circ_151129,RMVar_hsa_circ_151130,RMVar_hsa_circ_151131 3828 RMVar_ID_3828 Human_SNP_ID_470763493 A-to-I Human chr11 - 68067554 68067554 68067554 CTGTTACTGTGTCACCCAGGCTGGTGTGCAGTAGTGCAGTCTAGGCTCCACGTAACCTTAGCCTG CTGTTACTGTGTCACCCAGGCTGGTGTGCAGTGGTGCAGTCTAGGCTCCACGTAACCTTAGCCTG T C CHKA Ensembl:ENSG00000110721 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs976364985 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11772316 RMVar_hsa_circ_3019,RMVar_hsa_circ_77068,RMVar_hsa_circ_98826,RMVar_hsa_circ_11874,RMVar_hsa_circ_151130,RMVar_hsa_circ_151131,RMVar_hsa_circ_290829,RMVar_hsa_circ_357675,RMVar_hsa_circ_377684,RMVar_hsa_circ_29143,RMVar_hsa_circ_61492,RMVar_hsa_circ_151132,RMVar_hsa_circ_61762,RMVar_hsa_circ_320988,RMVar_hsa_circ_340594,RMVar_hsa_circ_21924,RMVar_hsa_circ_333132 3829 RMVar_ID_3829 Human_SNP_ID_470767466 A-to-I Human chr11 - 68084119 68084119 68084119 CCTCAGCCTCCTGAGTAGCTGGGATTACAGGCATGCGCCACTATGCCCGGCTAATTTTTTTGTAT CCTCAGCCTCCTGAGTAGCTGGGATTACAGGCGTGCGCCACTATGCCCGGCTAATTTTTTTGTAT T C CHKA Ensembl:ENSG00000110721 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1035840293 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3019,RMVar_hsa_circ_98826,RMVar_hsa_circ_151131,RMVar_hsa_circ_357675,RMVar_hsa_circ_61142,RMVar_hsa_circ_304060 3830 RMVar_ID_3830 Human_SNP_ID_470767941 A-to-I Human chr11 - 68085392 68085392 68085392 ACATAGTGAGATCTTGTCTCTACAAGAAAAAAAAAAAGGCTAGGTATGGTGGCACATGCCTGTGG ACATAGTGAGATCTTGTCTCTACAAGAAAAAATAAAAGGCTAGGTATGGTGGCACATGCCTGTGG T A CHKA Ensembl:ENSG00000110721 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1004388278 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11688604 RMVar_hsa_circ_3019,RMVar_hsa_circ_98826,RMVar_hsa_circ_151131,RMVar_hsa_circ_357675,RMVar_hsa_circ_61142,RMVar_hsa_circ_304060 3831 RMVar_ID_3831 Human_SNP_ID_470767951 A-to-I Human chr11 - 68085420 68085419 68085421 GCTCAGGAATTCAAGAGCAGCCTGGGTAACATAGTGAGATCTTGTCTCTACAAGAAAAAAAAAAA GCTCAGGAATTCAAGAGCAGCCTGGGTAACA__GTGAGATCTTGTCTCTACAAGAAAAAAAAAAA CTA C CHKA Ensembl:ENSG00000110721 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs901426432 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_3019,RMVar_hsa_circ_98826,RMVar_hsa_circ_151131,RMVar_hsa_circ_357675,RMVar_hsa_circ_61142,RMVar_hsa_circ_304060 3832 RMVar_ID_3832 Human_SNP_ID_470767954 A-to-I Human chr11 - 68085444 68085444 68085444 GACTGTGGCAGGAGGATCACTTGAGCTCAGGAATTCAAGAGCAGCCTGGGTAACATAGTGAGATC GACTGTGGCAGGAGGATCACTTGAGCTCAGGAGTTCAAGAGCAGCCTGGGTAACATAGTGAGATC T C CHKA Ensembl:ENSG00000110721 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs144934009 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11688605 RMVar_hsa_circ_3019,RMVar_hsa_circ_98826,RMVar_hsa_circ_151131,RMVar_hsa_circ_357675,RMVar_hsa_circ_61142,RMVar_hsa_circ_304060 3833 RMVar_ID_3833 Human_SNP_ID_470767968 A-to-I Human chr11 - 68085494 68085494 68085494 TTTTCAGGCTGGTCATGGTGGCTCATGCCTGTAATCTCAGCCCTTTGGGAGACTGTGGCAGGAGG TTTTCAGGCTGGTCATGGTGGCTCATGCCTGTCATCTCAGCCCTTTGGGAGACTGTGGCAGGAGG T G CHKA Ensembl:ENSG00000110721 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1158296669 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24899588,Human_RBP_ID_27557268 RMVar_hsa_circ_3019,RMVar_hsa_circ_98826,RMVar_hsa_circ_151131,RMVar_hsa_circ_357675,RMVar_hsa_circ_61142,RMVar_hsa_circ_304060 3834 RMVar_ID_3834 Human_SNP_ID_470768060 A-to-I Human chr11 - 68085901 68085901 68085901 TAAATAGCCGGGCGTGGTGGCACACACCTGTAATCCCAACTATTCCGGAGGCTGAGGTGGGAGAA TAAATAGCCGGGCGTGGTGGCACACACCTGTAGTCCCAACTATTCCGGAGGCTGAGGTGGGAGAA T C CHKA Ensembl:ENSG00000110721 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1252013284 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3019,RMVar_hsa_circ_98826,RMVar_hsa_circ_151131,RMVar_hsa_circ_357675,RMVar_hsa_circ_61142,RMVar_hsa_circ_304060 3835 RMVar_ID_3835 Human_SNP_ID_470768166 A-to-I Human chr11 - 68086305 68086305 68086305 ATTTTTTTTATTGTATTTTTATTTTATGAGACAGAGTCTCGCTGTCGCCAGGCTGGGGTGCAGTG ATTTTTTTTATTGTATTTTTATTTTATGAGACGGAGTCTCGCTGTCGCCAGGCTGGGGTGCAGTG T C CHKA Ensembl:ENSG00000110721 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1361929624 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11772320 RMVar_hsa_circ_3019,RMVar_hsa_circ_98826,RMVar_hsa_circ_151131,RMVar_hsa_circ_357675,RMVar_hsa_circ_61142,RMVar_hsa_circ_304060 3836 RMVar_ID_3836 Human_SNP_ID_470768208 A-to-I Human chr11 - 68086568 68086568 68086568 TTTGTTTTCATCTCCCAAATGGGGCTTTATTCATTTAGTCATAAACCTACTTCCCTCAGTATTAG TTTGTTTTCATCTCCCAAATGGGGCTTTATTCGTTTAGTCATAAACCTACTTCCCTCAGTATTAG T C CHKA Ensembl:ENSG00000110721 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2511439 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_98,GWAS_ID_99,GWAS_ID_100,GWAS_ID_101,GWAS_ID_102,GWAS_ID_103,GWAS_ID_104,GWAS_ID_105,GWAS_ID_106,GWAS_ID_107,GWAS_ID_108,GWAS_ID_109 RMVar_hsa_circ_3019,RMVar_hsa_circ_98826,RMVar_hsa_circ_151131,RMVar_hsa_circ_357675,RMVar_hsa_circ_61142,RMVar_hsa_circ_304060 3837 RMVar_ID_3837 Human_SNP_ID_470768611 A-to-I Human chr11 - 68088031 68088031 68088031 TTAGCTCGCGGCAACCTCTGCCTCTCAGGTTCAAGCGATTCTTATGCCTCAGTCCCCTGAGTAGC TTAGCTCGCGGCAACCTCTGCCTCTCAGGTTCGAGCGATTCTTATGCCTCAGTCCCCTGAGTAGC T C CHKA Ensembl:ENSG00000110721 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1464021707 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11688635 RMVar_hsa_circ_3019,RMVar_hsa_circ_98826,RMVar_hsa_circ_151131,RMVar_hsa_circ_357675,RMVar_hsa_circ_61142,RMVar_hsa_circ_304060 3838 RMVar_ID_3838 Human_SNP_ID_470769752 A-to-I Human chr11 - 68093140 68093140 68093140 AGCTGGGCGTGGTGGCATGTGCCTGTGGTCCCAGCAACTTTGGAGGCTGAGGTGAGAAGATCTCT AGCTGGGCGTGGTGGCATGTGCCTGTGGTCCCTGCAACTTTGGAGGCTGAGGTGAGAAGATCTCT T A CHKA Ensembl:ENSG00000110721 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1488351384 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3019,RMVar_hsa_circ_98826,RMVar_hsa_circ_151131,RMVar_hsa_circ_357675,RMVar_hsa_circ_61142,RMVar_hsa_circ_304060 3839 RMVar_ID_3839 Human_SNP_ID_470769775 A-to-I Human chr11 - 68093266 68093266 68093266 GCTGGTCATGGTGGCTCACTCCTGTAATTCCAACACTTTGGGAGGCCAAGGCAGGTGGATTGCTT GCTGGTCATGGTGGCTCACTCCTGTAATTCCAGCACTTTGGGAGGCCAAGGCAGGTGGATTGCTT T C CHKA Ensembl:ENSG00000110721 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs544931249 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3019,RMVar_hsa_circ_98826,RMVar_hsa_circ_151131,RMVar_hsa_circ_357675,RMVar_hsa_circ_61142,RMVar_hsa_circ_304060 3840 RMVar_ID_3840 Human_SNP_ID_470770050 A-to-I Human chr11 - 68094491 68094491 68094491 TGCCACCCAGGCTGTAGTGTAGTGGCACAACCATGGCTCACTGCAGCCTCGACCTCCTGGGCTCA TGCCACCCAGGCTGTAGTGTAGTGGCACAACCGTGGCTCACTGCAGCCTCGACCTCCTGGGCTCA T C CHKA Ensembl:ENSG00000110721 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048056992 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_108749,Human_RBP_ID_11688812 RMVar_hsa_circ_3019,RMVar_hsa_circ_98826,RMVar_hsa_circ_151131,RMVar_hsa_circ_357675,RMVar_hsa_circ_61142,RMVar_hsa_circ_304060 3841 RMVar_ID_3841 Human_SNP_ID_470770364 A-to-I Human chr11 - 68095646 68095646 68095646 GGTGTGCAGTGGTGCAATCTCGGCTTACTGCAAACTCTGCCTCCCGGGTTCACGCCATTCTCCTG GGTGTGCAGTGGTGCAATCTCGGCTTACTGCAGACTCTGCCTCCCGGGTTCACGCCATTCTCCTG T C CHKA Ensembl:ENSG00000110721 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1318271649 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3019,RMVar_hsa_circ_98826,RMVar_hsa_circ_151131,RMVar_hsa_circ_357675,RMVar_hsa_circ_61142,RMVar_hsa_circ_304060 3842 RMVar_ID_3842 Human_SNP_ID_470789492 A-to-I Human chr11 - 68168100 68168100 68168100 TCGATCTCAACTCACTGCAACCTTCACCTTCCAGGTTCACGCAATTCTTCTGCCTCAGCCTCCCG TCGATCTCAACTCACTGCAACCTTCACCTTCCGGGTTCACGCAATTCTTCTGCCTCAGCCTCCCG T C KMT5B Ensembl:ENSG00000110066 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1433719471 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_151136,RMVar_hsa_circ_81761,RMVar_hsa_circ_122141,RMVar_hsa_circ_151135,RMVar_hsa_circ_123985,RMVar_hsa_circ_103074,RMVar_hsa_circ_85456,RMVar_hsa_circ_151138,RMVar_hsa_circ_151140,RMVar_hsa_circ_151139,RMVar_hsa_circ_151137,RMVar_hsa_circ_151142,RMVar_hsa_circ_287675,RMVar_hsa_circ_308626,RMVar_hsa_circ_314953,RMVar_hsa_circ_358436,RMVar_hsa_circ_292053,RMVar_hsa_circ_151144,RMVar_hsa_circ_151145,RMVar_hsa_circ_151143 3843 RMVar_ID_3843 Human_SNP_ID_470789584 A-to-I Human chr11 - 68168476 68168476 68168476 CAAAAATTAGCCAGATGTGGTGGTGCGCGCCTATAATTCCAGCTACTCAGGAGGCTGAAGCAGGA CAAAAATTAGCCAGATGTGGTGGTGCGCGCCTGTAATTCCAGCTACTCAGGAGGCTGAAGCAGGA T C KMT5B Ensembl:ENSG00000110066 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs900287010 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_151136,RMVar_hsa_circ_81761,RMVar_hsa_circ_122141,RMVar_hsa_circ_151135,RMVar_hsa_circ_123985,RMVar_hsa_circ_103074,RMVar_hsa_circ_85456,RMVar_hsa_circ_151138,RMVar_hsa_circ_151140,RMVar_hsa_circ_151139,RMVar_hsa_circ_151137,RMVar_hsa_circ_151142,RMVar_hsa_circ_287675,RMVar_hsa_circ_308626,RMVar_hsa_circ_314953,RMVar_hsa_circ_358436,RMVar_hsa_circ_292053,RMVar_hsa_circ_151144,RMVar_hsa_circ_151145,RMVar_hsa_circ_151143 3844 RMVar_ID_3844 Human_SNP_ID_470791162 A-to-I Human chr11 - 68175096 68175096 68175096 AAGAAAGATGAACACTTGGAGAAAGCCTTCAAATGTTTGACTTCAGGCGAATGGGCACGGCACTA AAGAAAGATGAACACTTGGAGAAAGCCTTCAAGTGTTTGACTTCAGGCGAATGGGCACGGCACTA T C KMT5B Ensembl:ENSG00000110066 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1181600453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11689215,Human_RBP_ID_18611889 Human_Splice_Rec_1268274,Human_Splice_Rec_1268275,Human_Splice_Rec_1268292,Human_Splice_Rec_1268293,Human_Splice_Rec_1268310,Human_Splice_Rec_1268311,Human_Splice_Rec_1268332,Human_Splice_Rec_1268333,Human_Splice_Rec_1268352,Human_Splice_Rec_1268353,Human_Splice_Rec_1268370,Human_Splice_Rec_1268371,Human_Splice_Rec_1268388,Human_Splice_Rec_1268389,Human_Splice_Rec_1268406,Human_Splice_Rec_1268407,Human_Splice_Rec_1268418,Human_Splice_Rec_1268419,Human_Splice_Rec_1268430,Human_Splice_Rec_1268431,Human_Splice_Rec_1268436,Human_Splice_Rec_1268437,Human_Splice_Rec_1268446,Human_Splice_Rec_1268447,Human_Splice_Rec_1268454 RMVar_hsa_circ_151136,RMVar_hsa_circ_123985,RMVar_hsa_circ_103074,RMVar_hsa_circ_85456,RMVar_hsa_circ_151138,RMVar_hsa_circ_151137,RMVar_hsa_circ_6409,RMVar_hsa_circ_151147,RMVar_hsa_circ_151142,RMVar_hsa_circ_287675,RMVar_hsa_circ_308626,RMVar_hsa_circ_314953,RMVar_hsa_circ_358436,RMVar_hsa_circ_292053,RMVar_hsa_circ_151144,RMVar_hsa_circ_151145,RMVar_hsa_circ_151143,RMVar_hsa_circ_151149,RMVar_hsa_circ_296035,RMVar_hsa_circ_308110,RMVar_hsa_circ_355415,RMVar_hsa_circ_304832,RMVar_hsa_circ_151148,RMVar_hsa_circ_62875,RMVar_hsa_circ_355392,RMVar_hsa_circ_151146,RMVar_hsa_circ_360763,RMVar_hsa_circ_316213,RMVar_hsa_circ_314258,RMVar_hsa_circ_151150,RMVar_hsa_circ_359785,RMVar_hsa_circ_10331,RMVar_hsa_circ_151153,RMVar_hsa_circ_12537,RMVar_hsa_circ_151151,RMVar_hsa_circ_151152,RMVar_hsa_circ_300267,RMVar_hsa_circ_314067,RMVar_hsa_circ_288414,RMVar_hsa_circ_151154,RMVar_hsa_circ_151155 3845 RMVar_ID_3845 Human_SNP_ID_470795083 A-to-I Human chr11 - 68191124 68191124 68191124 GGATGTGGTGGCTCCTGCCTCTAGTCCCAGCTACTTGGGAGGCTGAGTGGGAGGATTGGTTGAGC GGATGTGGTGGCTCCTGCCTCTAGTCCCAGCTCCTTGGGAGGCTGAGTGGGAGGATTGGTTGAGC T G KMT5B Ensembl:ENSG00000110066 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1225991764 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_151136,RMVar_hsa_circ_123985 3846 RMVar_ID_3846 Human_SNP_ID_470844064 A-to-I Human chr11 + 68376289 68376289 68376289 CTGCAACCTCTGCCTGCTGAGCTCAAGCGATTATCCTGCCTCAGCCTCCCGAGTAGCTTGGACTA CTGCAACCTCTGCCTGCTGAGCTCAAGCGATTGTCCTGCCTCAGCCTCCCGAGTAGCTTGGACTA A G LRP5 Ensembl:ENSG00000162337 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1250513803 Functional Loss SNV dbSNP153 33..33 33 - - - 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 3847 RMVar_ID_3847 Human_SNP_ID_470844071 A-to-I Human chr11 + 68376321 68376321 68376321 ATCCTGCCTCAGCCTCCCGAGTAGCTTGGACTATAGGCACCCGCCACCACACTCGGCTTATTTTT ATCCTGCCTCAGCCTCCCGAGTAGCTTGGACTGTAGGCACCCGCCACCACACTCGGCTTATTTTT A G LRP5 Ensembl:ENSG00000162337 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1387783191 Functional Loss SNV dbSNP153 33..33 33 - - - 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 3848 RMVar_ID_3848 Human_SNP_ID_470844072 A-to-I Human chr11 + 68376323 68376323 68376323 CCTGCCTCAGCCTCCCGAGTAGCTTGGACTATAGGCACCCGCCACCACACTCGGCTTATTTTTTG CCTGCCTCAGCCTCCCGAGTAGCTTGGACTATGGGCACCCGCCACCACACTCGGCTTATTTTTTG A G LRP5 Ensembl:ENSG00000162337 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1373287394 Functional Loss SNV dbSNP153 33..33 33 - - - 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 3849 RMVar_ID_3849 Human_SNP_ID_470844720 A-to-I Human chr11 + 68378782 68378782 68378782 TTTTAGGGTCAGGCGCGGTGGCTCACACCTGTAATCCCAACACTTTGGGAGGCTGGAGTTGGGGT TTTTAGGGTCAGGCGCGGTGGCTCACACCTGTGATCCCAACACTTTGGGAGGCTGGAGTTGGGGT A G LRP5 Ensembl:ENSG00000162337 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1044374721 Functional Loss SNV dbSNP153 33..33 33 - - - 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 3850 RMVar_ID_3850 Human_SNP_ID_470862255 A-to-I Human chr11 + 68441182 68441182 68441182 CTAACTGCAGCCTCTACCTTCTAGGCTCAAGCAATCCTCCCATCTCAGCCCCTAAGTAGCTAGGA CTAACTGCAGCCTCTACCTTCTAGGCTCAAGCGATCCTCCCATCTCAGCCCCTAAGTAGCTAGGA A G LRP5 Ensembl:ENSG00000162337 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1565119786 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81769,RMVar_hsa_circ_151161 3851 RMVar_ID_3851 Human_SNP_ID_470862733 A-to-I Human chr11 + 68443232 68443232 68443232 TTGTGTGTTTAAGAACCTTTGGGCCCAGCGTGATGGCTTGCAGCTGTAATCTCAGCACTTTAGGA TTGTGTGTTTAAGAACCTTTGGGCCCAGCGTGTTGGCTTGCAGCTGTAATCTCAGCACTTTAGGA A T LRP5 Ensembl:ENSG00000162337 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs565998895 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81769,RMVar_hsa_circ_151161 3852 RMVar_ID_3852 Human_SNP_ID_470871750 A-to-I Human chr11 + 68474122 68474122 68474122 TGAAGTGCACTGTGGCATGATCATAGCTTACTACAGCTTCAAACTCCTGGGCTCAAGGAATCCTC TGAAGTGCACTGTGGCATGATCATAGCTTACTGCAGCTTCAAACTCCTGGGCTCAAGGAATCCTC A G PPP6R3 Ensembl:ENSG00000110075 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs377137037 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11759827 RMVar_hsa_circ_74130,RMVar_hsa_circ_350005,RMVar_hsa_circ_9301,RMVar_hsa_circ_41838 3853 RMVar_ID_3853 Human_SNP_ID_470873848 A-to-I Human chr11 + 68479838 68479837 68479839 CTGGCTCACTGTAGCCTCGGACACCTGGACTCATGTGATCCTCCCACCTCAGCCTCCCGAGTAGC CTGGCTCACTGTAGCCTCGGACACCTGGACTC__GTGATCCTCCCACCTCAGCCTCCCGAGTAGC CAT C PPP6R3 Ensembl:ENSG00000110075 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1253335543 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_2278733,Human_RBP_ID_8357416,Human_RBP_ID_11690730 RMVar_hsa_circ_74130,RMVar_hsa_circ_350005,RMVar_hsa_circ_9301,RMVar_hsa_circ_41838 3854 RMVar_ID_3854 Human_SNP_ID_470873849 A-to-I Human chr11 + 68479838 68479838 68479838 CTGGCTCACTGTAGCCTCGGACACCTGGACTCATGTGATCCTCCCACCTCAGCCTCCCGAGTAGC CTGGCTCACTGTAGCCTCGGACACCTGGACTCTTGTGATCCTCCCACCTCAGCCTCCCGAGTAGC A T PPP6R3 Ensembl:ENSG00000110075 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs754516036 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2278733,Human_RBP_ID_8357416,Human_RBP_ID_11690730 RMVar_hsa_circ_74130,RMVar_hsa_circ_350005,RMVar_hsa_circ_9301,RMVar_hsa_circ_41838 3855 RMVar_ID_3855 Human_SNP_ID_470873880 A-to-I Human chr11 + 68479966 68479966 68479966 TGCTATGTTGACCAGGCTGTTCTCTTGGGCTCAAGTGATTATCCTGCCTTGCCCTCCCAAAGTGC TGCTATGTTGACCAGGCTGTTCTCTTGGGCTCGAGTGATTATCCTGCCTTGCCCTCCCAAAGTGC A G PPP6R3 Ensembl:ENSG00000110075 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903772885 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11690738,Human_RBP_ID_23517711 RMVar_hsa_circ_74130,RMVar_hsa_circ_350005,RMVar_hsa_circ_9301,RMVar_hsa_circ_41838 3856 RMVar_ID_3856 Human_SNP_ID_470876971 A-to-I Human chr11 + 68491597 68491597 68491597 GTCCTGAACTTCTGGGCTCAAGCAGTCCTCCTACTTCAGCCTCCTAAAGTGTCGGGATTATAGGT GTCCTGAACTTCTGGGCTCAAGCAGTCCTCCTGCTTCAGCCTCCTAAAGTGTCGGGATTATAGGT A G PPP6R3 Ensembl:ENSG00000110075 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs918459237 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74130,RMVar_hsa_circ_350005,RMVar_hsa_circ_9301,RMVar_hsa_circ_41838 3857 RMVar_ID_3857 Human_SNP_ID_470882700 A-to-I Human chr11 + 68512827 68512826 68512827 ACAAAACGTCAGGTATGAATGTCTGCCCTTACAAACCTTTTGTGCTGGCATTGTACAAGTGCTTG ACAAAACGTCAGGTATGAATGTCTGCCCTTAC_AACCTTTTGTGCTGGCATTGTACAAGTGCTTG CA C PPP6R3 Ensembl:ENSG00000110075 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1208244947 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_151209,RMVar_hsa_circ_273670,RMVar_hsa_circ_324989,RMVar_hsa_circ_74130,RMVar_hsa_circ_350005,RMVar_hsa_circ_9301,RMVar_hsa_circ_41838,RMVar_hsa_circ_357453,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_297619,RMVar_hsa_circ_275384,RMVar_hsa_circ_293288,RMVar_hsa_circ_274270,RMVar_hsa_circ_151213,RMVar_hsa_circ_151215,RMVar_hsa_circ_107895,RMVar_hsa_circ_151214,RMVar_hsa_circ_151211,RMVar_hsa_circ_151212,RMVar_hsa_circ_151210,RMVar_hsa_circ_151207,RMVar_hsa_circ_151208 3858 RMVar_ID_3858 Human_SNP_ID_470887957 A-to-I Human chr11 + 68533594 68533594 68533594 AGGTGTGGTGGCACGGGTCTGTAGTCTCAGCTACTCTGGAGGCTGAGGTGGGAGGATCACCTGAG AGGTGTGGTGGCACGGGTCTGTAGTCTCAGCTGCTCTGGAGGCTGAGGTGGGAGGATCACCTGAG A G PPP6R3 Ensembl:ENSG00000110075 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1286175736 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45873,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_297619,RMVar_hsa_circ_275384,RMVar_hsa_circ_151213,RMVar_hsa_circ_107895,RMVar_hsa_circ_151214,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_363621,RMVar_hsa_circ_318141,RMVar_hsa_circ_74196,RMVar_hsa_circ_56180,RMVar_hsa_circ_56741,RMVar_hsa_circ_49309,RMVar_hsa_circ_270973,RMVar_hsa_circ_315360,RMVar_hsa_circ_151217,RMVar_hsa_circ_329286,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_151218 3859 RMVar_ID_3859 Human_SNP_ID_470897947 A-to-I Human chr11 + 68572668 68572668 68572668 GGCCAGGGGTTCGAGACCAGTCTGGACAACATAGGGAGATCCTGGCTCTACAAAAAATTAGCCGG GGCCAGGGGTTCGAGACCAGTCTGGACAACATGGGGAGATCCTGGCTCTACAAAAAATTAGCCGG A G PPP6R3 Ensembl:ENSG00000110075 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs939110972 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_151209,RMVar_hsa_circ_324989,RMVar_hsa_circ_9301,RMVar_hsa_circ_41838,RMVar_hsa_circ_373954,RMVar_hsa_circ_107895,RMVar_hsa_circ_341886,RMVar_hsa_circ_151207,RMVar_hsa_circ_151208,RMVar_hsa_circ_74196,RMVar_hsa_circ_49309,RMVar_hsa_circ_315360,RMVar_hsa_circ_329940,RMVar_hsa_circ_322361,RMVar_hsa_circ_27823,RMVar_hsa_circ_52327,RMVar_hsa_circ_151222,RMVar_hsa_circ_151223,RMVar_hsa_circ_16302,RMVar_hsa_circ_306222,RMVar_hsa_circ_64476,RMVar_hsa_circ_151229,RMVar_hsa_circ_151230,RMVar_hsa_circ_97759,RMVar_hsa_circ_300116,RMVar_hsa_circ_151234,RMVar_hsa_circ_349824,RMVar_hsa_circ_366475,RMVar_hsa_circ_296401,RMVar_hsa_circ_274025,RMVar_hsa_circ_151236,RMVar_hsa_circ_151237,RMVar_hsa_circ_151235,RMVar_hsa_circ_84137,RMVar_hsa_circ_341477,RMVar_hsa_circ_69345,RMVar_hsa_circ_151243,RMVar_hsa_circ_344130,RMVar_hsa_circ_336680,RMVar_hsa_circ_42205,RMVar_hsa_circ_275013,RMVar_hsa_circ_151246,RMVar_hsa_circ_151244,RMVar_hsa_circ_151245,RMVar_hsa_circ_354165,RMVar_hsa_circ_362768,RMVar_hsa_circ_320682,RMVar_hsa_circ_288113,RMVar_hsa_circ_151248,RMVar_hsa_circ_151249,RMVar_hsa_circ_151247,RMVar_hsa_circ_47787,RMVar_hsa_circ_321006,RMVar_hsa_circ_333424,RMVar_hsa_circ_360142,RMVar_hsa_circ_57535,RMVar_hsa_circ_278579,RMVar_hsa_circ_321720,RMVar_hsa_circ_286808,RMVar_hsa_circ_278438,RMVar_hsa_circ_151251,RMVar_hsa_circ_151253,RMVar_hsa_circ_151254,RMVar_hsa_circ_151252,RMVar_hsa_circ_68037,RMVar_hsa_circ_279641,RMVar_hsa_circ_285278,RMVar_hsa_circ_368277,RMVar_hsa_circ_151250,RMVar_hsa_circ_336249,RMVar_hsa_circ_284914,RMVar_hsa_circ_273918,RMVar_hsa_circ_151255,RMVar_hsa_circ_151257,RMVar_hsa_circ_151258,RMVar_hsa_circ_151256 3860 RMVar_ID_3860 Human_SNP_ID_470897962 A-to-I Human chr11 + 68572711 68572711 68572711 GGCTCTACAAAAAATTAGCCGGATGTGGTGGTACTTGCCTATAGTCCCAGCTACTCAAGAGGCCG GGCTCTACAAAAAATTAGCCGGATGTGGTGGTGCTTGCCTATAGTCCCAGCTACTCAAGAGGCCG A G PPP6R3 Ensembl:ENSG00000110075 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs576011719 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_151209,RMVar_hsa_circ_324989,RMVar_hsa_circ_9301,RMVar_hsa_circ_41838,RMVar_hsa_circ_373954,RMVar_hsa_circ_107895,RMVar_hsa_circ_341886,RMVar_hsa_circ_151207,RMVar_hsa_circ_151208,RMVar_hsa_circ_74196,RMVar_hsa_circ_49309,RMVar_hsa_circ_315360,RMVar_hsa_circ_329940,RMVar_hsa_circ_322361,RMVar_hsa_circ_27823,RMVar_hsa_circ_52327,RMVar_hsa_circ_151222,RMVar_hsa_circ_151223,RMVar_hsa_circ_16302,RMVar_hsa_circ_306222,RMVar_hsa_circ_64476,RMVar_hsa_circ_151229,RMVar_hsa_circ_151230,RMVar_hsa_circ_97759,RMVar_hsa_circ_300116,RMVar_hsa_circ_151234,RMVar_hsa_circ_349824,RMVar_hsa_circ_366475,RMVar_hsa_circ_296401,RMVar_hsa_circ_274025,RMVar_hsa_circ_151236,RMVar_hsa_circ_151237,RMVar_hsa_circ_151235,RMVar_hsa_circ_84137,RMVar_hsa_circ_341477,RMVar_hsa_circ_69345,RMVar_hsa_circ_151243,RMVar_hsa_circ_344130,RMVar_hsa_circ_336680,RMVar_hsa_circ_42205,RMVar_hsa_circ_275013,RMVar_hsa_circ_151246,RMVar_hsa_circ_151244,RMVar_hsa_circ_151245,RMVar_hsa_circ_354165,RMVar_hsa_circ_362768,RMVar_hsa_circ_320682,RMVar_hsa_circ_288113,RMVar_hsa_circ_151248,RMVar_hsa_circ_151249,RMVar_hsa_circ_151247,RMVar_hsa_circ_47787,RMVar_hsa_circ_321006,RMVar_hsa_circ_333424,RMVar_hsa_circ_360142,RMVar_hsa_circ_57535,RMVar_hsa_circ_278579,RMVar_hsa_circ_321720,RMVar_hsa_circ_286808,RMVar_hsa_circ_278438,RMVar_hsa_circ_151251,RMVar_hsa_circ_151253,RMVar_hsa_circ_151254,RMVar_hsa_circ_151252,RMVar_hsa_circ_68037,RMVar_hsa_circ_279641,RMVar_hsa_circ_285278,RMVar_hsa_circ_368277,RMVar_hsa_circ_151250,RMVar_hsa_circ_336249,RMVar_hsa_circ_284914,RMVar_hsa_circ_273918,RMVar_hsa_circ_151255,RMVar_hsa_circ_151257,RMVar_hsa_circ_151258,RMVar_hsa_circ_151256 3861 RMVar_ID_3861 Human_SNP_ID_470899032 A-to-I Human chr11 + 68576290 68576290 68576290 TTGAGAAGTCACTGATTTCTGCTCCACATCCTACTTAGTGTCCATTTCCCTCCATGCCCTGCTGC TTGAGAAGTCACTGATTTCTGCTCCACATCCTGCTTAGTGTCCATTTCCCTCCATGCCCTGCTGC A G PPP6R3 Ensembl:ENSG00000110075 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559051289 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11694030 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 3862 RMVar_ID_3862 Human_SNP_ID_470902159 A-to-I Human chr11 + 68588623 68588623 68588623 GGGACTACAGGTACCCGCCACCGCACCTGGCTAATTTGTTGTATTTTTAGTAGAGACGGGATTTC GGGACTACAGGTACCCGCCACCGCACCTGGCTGATTTGTTGTATTTTTAGTAGAGACGGGATTTC A G PPP6R3 Ensembl:ENSG00000110075 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984839077 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_373954,RMVar_hsa_circ_107895,RMVar_hsa_circ_151207,RMVar_hsa_circ_151208,RMVar_hsa_circ_74196,RMVar_hsa_circ_27823,RMVar_hsa_circ_52327,RMVar_hsa_circ_16302,RMVar_hsa_circ_151230,RMVar_hsa_circ_97759,RMVar_hsa_circ_151234,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_336680,RMVar_hsa_circ_7008,RMVar_hsa_circ_63560,RMVar_hsa_circ_151245,RMVar_hsa_circ_288113,RMVar_hsa_circ_151249,RMVar_hsa_circ_47787,RMVar_hsa_circ_360142,RMVar_hsa_circ_57535,RMVar_hsa_circ_278579,RMVar_hsa_circ_321720,RMVar_hsa_circ_151251,RMVar_hsa_circ_68037,RMVar_hsa_circ_151250,RMVar_hsa_circ_284914,RMVar_hsa_circ_273918,RMVar_hsa_circ_151257,RMVar_hsa_circ_151258,RMVar_hsa_circ_359879,RMVar_hsa_circ_91518,RMVar_hsa_circ_47055,RMVar_hsa_circ_151261,RMVar_hsa_circ_45076,RMVar_hsa_circ_151264,RMVar_hsa_circ_68443,RMVar_hsa_circ_308617,RMVar_hsa_circ_363875,RMVar_hsa_circ_271968,RMVar_hsa_circ_151265,RMVar_hsa_circ_151263,RMVar_hsa_circ_151266,RMVar_hsa_circ_302939,RMVar_hsa_circ_328515,RMVar_hsa_circ_63947,RMVar_hsa_circ_19266 3863 RMVar_ID_3863 Human_SNP_ID_470902262 A-to-I Human chr11 + 68588949 68588949 68588949 TTAATCCTGGCCTGGCATAGTGGCTCACACCTATAATCCCAGCACTTTGGGAGGCCGAGCCGGGC TTAATCCTGGCCTGGCATAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGCCGGGC A G PPP6R3 Ensembl:ENSG00000110075 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs976321574 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24900401 RMVar_hsa_circ_373954,RMVar_hsa_circ_107895,RMVar_hsa_circ_151207,RMVar_hsa_circ_151208,RMVar_hsa_circ_74196,RMVar_hsa_circ_27823,RMVar_hsa_circ_52327,RMVar_hsa_circ_16302,RMVar_hsa_circ_151230,RMVar_hsa_circ_97759,RMVar_hsa_circ_151234,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_336680,RMVar_hsa_circ_7008,RMVar_hsa_circ_63560,RMVar_hsa_circ_151245,RMVar_hsa_circ_288113,RMVar_hsa_circ_151249,RMVar_hsa_circ_47787,RMVar_hsa_circ_360142,RMVar_hsa_circ_57535,RMVar_hsa_circ_278579,RMVar_hsa_circ_321720,RMVar_hsa_circ_151251,RMVar_hsa_circ_68037,RMVar_hsa_circ_151250,RMVar_hsa_circ_284914,RMVar_hsa_circ_273918,RMVar_hsa_circ_151257,RMVar_hsa_circ_151258,RMVar_hsa_circ_359879,RMVar_hsa_circ_91518,RMVar_hsa_circ_47055,RMVar_hsa_circ_151261,RMVar_hsa_circ_45076,RMVar_hsa_circ_151264,RMVar_hsa_circ_68443,RMVar_hsa_circ_308617,RMVar_hsa_circ_363875,RMVar_hsa_circ_271968,RMVar_hsa_circ_151265,RMVar_hsa_circ_151263,RMVar_hsa_circ_151266,RMVar_hsa_circ_302939,RMVar_hsa_circ_328515,RMVar_hsa_circ_63947,RMVar_hsa_circ_19266 3864 RMVar_ID_3864 Human_SNP_ID_470944972 A-to-I Human chr11 - 68755534 68755534 68755534 GTGGTGGCGGGCGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATGGCGTGAACCCG GTGGTGGCGGGCGCCTGTAGTCCCAGCTACTCTGGAGGCTGAGGCAGGAGAATGGCGTGAACCCG T A CPT1A Ensembl:ENSG00000110090 Protein coding intron GSE47997;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 23474544,31158229,31158229 RNA-Seq:(High) rs547364161 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94639,RMVar_hsa_circ_121891,RMVar_hsa_circ_151282,RMVar_hsa_circ_151283 3865 RMVar_ID_3865 Human_SNP_ID_470944973 A-to-I Human chr11 - 68755534 68755534 68755534 GTGGTGGCGGGCGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATGGCGTGAACCCG GTGGTGGCGGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCG T C CPT1A Ensembl:ENSG00000110090 Protein coding intron GSE47997;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 23474544,31158229,31158229 RNA-Seq:(High) rs547364161 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94639,RMVar_hsa_circ_121891,RMVar_hsa_circ_151282,RMVar_hsa_circ_151283 3866 RMVar_ID_3866 Human_SNP_ID_470944974 A-to-I Human chr11 - 68755534 68755534 68755534 GTGGTGGCGGGCGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATGGCGTGAACCCG GTGGTGGCGGGCGCCTGTAGTCCCAGCTACTCCGGAGGCTGAGGCAGGAGAATGGCGTGAACCCG T G CPT1A Ensembl:ENSG00000110090 Protein coding intron GSE47997;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 23474544,31158229,31158229 RNA-Seq:(High) rs547364161 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94639,RMVar_hsa_circ_121891,RMVar_hsa_circ_151282,RMVar_hsa_circ_151283 3867 RMVar_ID_3867 Human_SNP_ID_470944976 A-to-I Human chr11 - 68755538 68755538 68755538 GGGCGTGGTGGCGGGCGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATGGCGTGAA GGGCGTGGTGGCGGGCGCCTGTAGTCCCAGCTGCTCAGGAGGCTGAGGCAGGAGAATGGCGTGAA T C CPT1A Ensembl:ENSG00000110090 Protein coding intron GSE47997;GSE126723:GSM3611827,GSM3611828,GSM3611829 K562 cells&HepG2 cells;Bronchiolar epithelium,BEP2D cell line - 23474544,31158229 RNA-Seq:(High) rs1461804726 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94639,RMVar_hsa_circ_121891,RMVar_hsa_circ_151282,RMVar_hsa_circ_151283 3868 RMVar_ID_3868 Human_SNP_ID_470944980 A-to-I Human chr11 - 68755548 68755548 68755548 AAAATGAGCCGGGCGTGGTGGCGGGCGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGA AAAATGAGCCGGGCGTGGTGGCGGGCGCCTGTGGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGA T C CPT1A Ensembl:ENSG00000110090 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1005987095 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94639,RMVar_hsa_circ_121891,RMVar_hsa_circ_151282,RMVar_hsa_circ_151283 3869 RMVar_ID_3869 Human_SNP_ID_470945013 A-to-I Human chr11 - 68755612 68755612 68755612 GAGGTCAGGAGATGGAGACCATCCTGGCTAACACGGTGAAACCCCGTCTCTACTAAAAATTCAAA GAGGTCAGGAGATGGAGACCATCCTGGCTAACGCGGTGAAACCCCGTCTCTACTAAAAATTCAAA T C CPT1A Ensembl:ENSG00000110090 Protein coding intron GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459,32596459 RNA-Seq:(High) rs1481822045 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_108597 RMVar_hsa_circ_94639,RMVar_hsa_circ_121891,RMVar_hsa_circ_151282,RMVar_hsa_circ_151283 3870 RMVar_ID_3870 Human_SNP_ID_470945038 A-to-I Human chr11 - 68755660 68755660 68755660 TCATGCGTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGCGGATCACGAGGTCAGGAGATGGAG TCATGCGTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGGATCACGAGGTCAGGAGATGGAG T C CPT1A Ensembl:ENSG00000110090 Protein coding intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1259222066 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2217971 RMVar_hsa_circ_94639,RMVar_hsa_circ_121891,RMVar_hsa_circ_151282,RMVar_hsa_circ_151283 3871 RMVar_ID_3871 Human_SNP_ID_470945115 A-to-I Human chr11 - 68755879 68755879 68755879 GAACTCCTGACCTCAGGTGATCCACCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAG GAACTCCTGACCTCAGGTGATCCACCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAG T C CPT1A Ensembl:ENSG00000110090 Protein coding intron GSE38233;GSE99789;GSE107867;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,EC109;ASD brains,Fragile X samples from NIH NeuroBioBank;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29796672,30559470,32596459 RNA-Seq:(High) rs1275084057 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_108599 Human_miRNA_ID_1394146,Human_miRNA_ID_2714754,Human_miRNA_ID_3050738 RMVar_hsa_circ_94639,RMVar_hsa_circ_121891,RMVar_hsa_circ_151282,RMVar_hsa_circ_151283 3872 RMVar_ID_3872 Human_SNP_ID_470945117 A-to-I Human chr11 - 68755888 68755888 68755888 GCTGGTCTCGAACTCCTGACCTCAGGTGATCCACCTGCCTCAGCCTCCCAAAGTGCTGGGATTAC GCTGGTCTCGAACTCCTGACCTCAGGTGATCCGCCTGCCTCAGCCTCCCAAAGTGCTGGGATTAC T C CPT1A Ensembl:ENSG00000110090 Protein coding intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1196278790 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_108599 Human_miRNA_ID_2714754,Human_miRNA_ID_3050738 RMVar_hsa_circ_94639,RMVar_hsa_circ_121891,RMVar_hsa_circ_151282,RMVar_hsa_circ_151283 3873 RMVar_ID_3873 Human_SNP_ID_470945132 A-to-I Human chr11 - 68755931 68755929 68755932 TTTTGTATTTTTAGTAGAGACGGGGTTTCATCATATTGGTCAGGCTGGTCTCGAACTCCTGACCT TTTTGTATTTTTAGTAGAGACGGGGTTTCAT___ATTGGTCAGGCTGGTCTCGAACTCCTGACCT TATG T CPT1A Ensembl:ENSG00000110090 Protein coding intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1171781751 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_94639,RMVar_hsa_circ_121891,RMVar_hsa_circ_151282,RMVar_hsa_circ_151283 3874 RMVar_ID_3874 Human_SNP_ID_470945133 A-to-I Human chr11 - 68755929 68755929 68755929 TTGTATTTTTAGTAGAGACGGGGTTTCATCATATTGGTCAGGCTGGTCTCGAACTCCTGACCTCA TTGTATTTTTAGTAGAGACGGGGTTTCATCATGTTGGTCAGGCTGGTCTCGAACTCCTGACCTCA T C CPT1A Ensembl:ENSG00000110090 Protein coding intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1415471550 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94639,RMVar_hsa_circ_121891,RMVar_hsa_circ_151282,RMVar_hsa_circ_151283 3875 RMVar_ID_3875 Human_SNP_ID_470945157 A-to-I Human chr11 - 68756000 68756000 68756000 TCAAGCGATTCTCCTGTCTCAGCCTCCCAAGTAGCTGGGATTACACGCCCAACACCATGCCCTGC TCAAGCGATTCTCCTGTCTCAGCCTCCCAAGTTGCTGGGATTACACGCCCAACACCATGCCCTGC T A CPT1A Ensembl:ENSG00000110090 Protein coding intron GSE47997;GSE100210;GSE99789;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,29129909,29796672,32596459 RNA-Seq:(High) rs1371671710 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17560057 RMVar_hsa_circ_94639,RMVar_hsa_circ_121891,RMVar_hsa_circ_151282,RMVar_hsa_circ_151283 3876 RMVar_ID_3876 Human_SNP_ID_470945162 A-to-I Human chr11 - 68756025 68756025 68756025 TCACTGCAGCATCTGCCTTGCAGGTTCAAGCGATTCTCCTGTCTCAGCCTCCCAAGTAGCTGGGA TCACTGCAGCATCTGCCTTGCAGGTTCAAGCGGTTCTCCTGTCTCAGCCTCCCAAGTAGCTGGGA T C CPT1A Ensembl:ENSG00000110090 Protein coding intron GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs1311590215 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_108601 RMVar_hsa_circ_94639,RMVar_hsa_circ_121891,RMVar_hsa_circ_151282,RMVar_hsa_circ_151283 3877 RMVar_ID_3877 Human_SNP_ID_470945165 A-to-I Human chr11 - 68756029 68756029 68756029 CGGCTCACTGCAGCATCTGCCTTGCAGGTTCAAGCGATTCTCCTGTCTCAGCCTCCCAAGTAGCT CGGCTCACTGCAGCATCTGCCTTGCAGGTTCAGGCGATTCTCCTGTCTCAGCCTCCCAAGTAGCT T C CPT1A Ensembl:ENSG00000110090 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 29129909,30559470 RNA-Seq:(High) rs931288317 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_108601 RMVar_hsa_circ_94639,RMVar_hsa_circ_121891,RMVar_hsa_circ_151282,RMVar_hsa_circ_151283 3878 RMVar_ID_3878 Human_SNP_ID_470945166 A-to-I Human chr11 - 68756036 68756036 68756036 GCAATCTCGGCTCACTGCAGCATCTGCCTTGCAGGTTCAAGCGATTCTCCTGTCTCAGCCTCCCA GCAATCTCGGCTCACTGCAGCATCTGCCTTGCGGGTTCAAGCGATTCTCCTGTCTCAGCCTCCCA T C CPT1A Ensembl:ENSG00000110090 Protein coding intron GSE38233;GSE100210;GSE107867;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;ASD brains,temporal_cortex;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,30559470,32596459 RNA-Seq:(High) rs547295948 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94639,RMVar_hsa_circ_121891,RMVar_hsa_circ_151282,RMVar_hsa_circ_151283 3879 RMVar_ID_3879 Human_SNP_ID_470945175 A-to-I Human chr11 - 68756065 68756065 68756065 TCTTGTTGCCCAGGCTGGAGTGCAGTGGTGCAATCTCGGCTCACTGCAGCATCTGCCTTGCAGGT TCTTGTTGCCCAGGCTGGAGTGCAGTGGTGCAGTCTCGGCTCACTGCAGCATCTGCCTTGCAGGT T C CPT1A Ensembl:ENSG00000110090 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs993265268 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94639,RMVar_hsa_circ_121891,RMVar_hsa_circ_151282,RMVar_hsa_circ_151283 3880 RMVar_ID_3880 Human_SNP_ID_470945184 A-to-I Human chr11 - 68756099 68756099 68756099 TTTTTTTTTTTTTTTTTTTGAGATGGAGTTTCACTCTTGTTGCCCAGGCTGGAGTGCAGTGGTGC TTTTTTTTTTTTTTTTTTTGAGATGGAGTTTCGCTCTTGTTGCCCAGGCTGGAGTGCAGTGGTGC T C CPT1A Ensembl:ENSG00000110090 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1478487758 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94639,RMVar_hsa_circ_121891,RMVar_hsa_circ_151282,RMVar_hsa_circ_151283 3881 RMVar_ID_3881 Human_SNP_ID_470958521 A-to-I Human chr11 - 68808871 68808871 68808871 GAACTCCTGGACCCAAGTGATCCACCCATCTCAGCCTCCCAAAGTGCTGGGATTATAGACTTGAG GAACTCCTGGACCCAAGTGATCCACCCATCTCTGCCTCCCAAAGTGCTGGGATTATAGACTTGAG T A CPT1A Ensembl:ENSG00000110090 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1055138449 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40006,RMVar_hsa_circ_151289,RMVar_hsa_circ_100355,RMVar_hsa_circ_151301,RMVar_hsa_circ_355338,RMVar_hsa_circ_342205,RMVar_hsa_circ_349947,RMVar_hsa_circ_151306,RMVar_hsa_circ_55858,RMVar_hsa_circ_151315,RMVar_hsa_circ_343058,RMVar_hsa_circ_311028,RMVar_hsa_circ_151318,RMVar_hsa_circ_104805,RMVar_hsa_circ_151316,RMVar_hsa_circ_280013,RMVar_hsa_circ_151319,RMVar_hsa_circ_264857,RMVar_hsa_circ_279055,RMVar_hsa_circ_151320 3882 RMVar_ID_3882 Human_SNP_ID_470958522 A-to-I Human chr11 - 68808871 68808871 68808871 GAACTCCTGGACCCAAGTGATCCACCCATCTCAGCCTCCCAAAGTGCTGGGATTATAGACTTGAG GAACTCCTGGACCCAAGTGATCCACCCATCTCGGCCTCCCAAAGTGCTGGGATTATAGACTTGAG T C CPT1A Ensembl:ENSG00000110090 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1055138449 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40006,RMVar_hsa_circ_151289,RMVar_hsa_circ_100355,RMVar_hsa_circ_151301,RMVar_hsa_circ_355338,RMVar_hsa_circ_342205,RMVar_hsa_circ_349947,RMVar_hsa_circ_151306,RMVar_hsa_circ_55858,RMVar_hsa_circ_151315,RMVar_hsa_circ_343058,RMVar_hsa_circ_311028,RMVar_hsa_circ_151318,RMVar_hsa_circ_104805,RMVar_hsa_circ_151316,RMVar_hsa_circ_280013,RMVar_hsa_circ_151319,RMVar_hsa_circ_264857,RMVar_hsa_circ_279055,RMVar_hsa_circ_151320 3883 RMVar_ID_3883 Human_SNP_ID_470976379 A-to-I Human chr11 - 68877273 68877273 68877273 GCCCAGCTAATTTTTGTATTTGTAGTAGAGATAGGGTTTAATCATATTGCCCAGGCTGGTCTCAA GCCCAGCTAATTTTTGTATTTGTAGTAGAGATGGGGTTTAATCATATTGCCCAGGCTGGTCTCAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs938729900 Functional Loss SNV dbSNP153 33..33 33 - - - 3884 RMVar_ID_3884 Human_SNP_ID_470977527 A-to-I Human chr11 - 68881922 68881922 68881922 ACGGTGGCTTACACCTGTAATCCCAGCACTTTAGGAGGCTGAGGCATGTGGATCTCTTGAGCTCA ACGGTGGCTTACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGCATGTGGATCTCTTGAGCTCA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053568200 Functional Loss SNV dbSNP153 33..33 33 - - - 3885 RMVar_ID_3885 Human_SNP_ID_470981276 A-to-I Human chr11 - 68895826 68895826 68895826 TCTCTACTAAAATTCCAAACAATTAGGTGGGCATGGTGGCACACACATGTAGTCCCAGCTATTTG TCTCTACTAAAATTCCAAACAATTAGGTGGGCTTGGTGGCACACACATGTAGTCCCAGCTATTTG T A MRPL21 Ensembl:ENSG00000197345 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1167159119 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_310704 3886 RMVar_ID_3886 Human_SNP_ID_470985792 A-to-I Human chr11 + 68912129 68912129 68912129 ATTATTATTCACTTACATTTTAAATTTTTTTTATTTTTATTTTTTGGAGACGGAGCCTCACTCTG ATTATTATTCACTTACATTTTAAATTTTTTTTGTTTTTATTTTTTGGAGACGGAGCCTCACTCTG A G IGHMBP2 Ensembl:ENSG00000132740 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1301595999 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6090281 RMVar_hsa_circ_116802,RMVar_hsa_circ_45858,RMVar_hsa_circ_151326 3887 RMVar_ID_3887 Human_SNP_ID_470985832 A-to-I Human chr11 + 68912297 68912296 68912297 GGGATTATAGGCGTGCGCCACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGATGGAGTTTCA GGGATTATAGGCGTGCGCCACCATGCCTGGCT_ATTTTTGTATTTTTAGTAGAGATGGAGTTTCA TA T IGHMBP2 Ensembl:ENSG00000132740 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1309716003 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_116802,RMVar_hsa_circ_45858,RMVar_hsa_circ_151326 3888 RMVar_ID_3888 Human_SNP_ID_470985835 A-to-I Human chr11 + 68912315 68912315 68912315 CACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGATGGAGTTTCACCACATTGGCCAGTCTGG CACCATGCCTGGCTAATTTTTGTATTTTTAGTGGAGATGGAGTTTCACCACATTGGCCAGTCTGG A G IGHMBP2 Ensembl:ENSG00000132740 Protein coding intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1223274397 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116802,RMVar_hsa_circ_45858,RMVar_hsa_circ_151326 3889 RMVar_ID_3889 Human_SNP_ID_470985842 A-to-I Human chr11 + 68912334 68912334 68912334 TTGTATTTTTAGTAGAGATGGAGTTTCACCACATTGGCCAGTCTGGTCTCACTCCTGACTTCAGT TTGTATTTTTAGTAGAGATGGAGTTTCACCACGTTGGCCAGTCTGGTCTCACTCCTGACTTCAGT A G IGHMBP2 Ensembl:ENSG00000132740 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1296461426 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116802,RMVar_hsa_circ_45858,RMVar_hsa_circ_151326 3890 RMVar_ID_3890 Human_SNP_ID_470985968 A-to-I Human chr11 + 68912856 68912856 68912856 GAGGTCAGGAGTTCGAGACCAGCCTGGCTAACATGGTGAAACCCCGTCTCTACTAAAAATACAAA GAGGTCAGGAGTTCGAGACCAGCCTGGCTAACGTGGTGAAACCCCGTCTCTACTAAAAATACAAA A G IGHMBP2 Ensembl:ENSG00000132740 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1436080906 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116802,RMVar_hsa_circ_45858,RMVar_hsa_circ_151326 3891 RMVar_ID_3891 Human_SNP_ID_470986201 A-to-I Human chr11 + 68913520 68913520 68913520 CTTTTTTTTTTCCTCAGAGATGGGGTCTCACTATGTTGTCCAGGGTGGTCTTAAACTCCTGACCT CTTTTTTTTTTCCTCAGAGATGGGGTCTCACTGTGTTGTCCAGGGTGGTCTTAAACTCCTGACCT A G IGHMBP2 Ensembl:ENSG00000132740 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs995829788 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116802,RMVar_hsa_circ_45858,RMVar_hsa_circ_151326 3892 RMVar_ID_3892 Human_SNP_ID_470986244 A-to-I Human chr11 + 68913655 68913655 68913655 AATAGTGGAGCTGTGGCTGGGTGCAGCGGCTCATGTCTGTTATCCTAGCGCTTTGGGAGGCCAAG AATAGTGGAGCTGTGGCTGGGTGCAGCGGCTCCTGTCTGTTATCCTAGCGCTTTGGGAGGCCAAG A C IGHMBP2 Ensembl:ENSG00000132740 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1282730688 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22000854 RMVar_hsa_circ_116802,RMVar_hsa_circ_45858,RMVar_hsa_circ_151326 3893 RMVar_ID_3893 Human_SNP_ID_471030191 A-to-I Human chr11 + 69074721 69074721 69074721 AAATTGTTACAAGGAGAAGGTGTTCGTATGTTAGCTGTGTAACTGAGAGATAACTGATATGACTA AAATTGTTACAAGGAGAAGGTGTTCGTATGTTTGCTGTGTAACTGAGAGATAACTGATATGACTA A T TPCN2,AP003071.5 Ensembl:ENSG00000162341,Ensembl:ENSG00000287725 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1295831823 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23267280,Human_RBP_ID_23518532 RMVar_hsa_circ_62262,RMVar_hsa_circ_125482,RMVar_hsa_circ_151331,RMVar_hsa_circ_91499,RMVar_hsa_circ_41535,RMVar_hsa_circ_69680,RMVar_hsa_circ_109303,RMVar_hsa_circ_151333,RMVar_hsa_circ_86579,RMVar_hsa_circ_151334,RMVar_hsa_circ_151335,RMVar_hsa_circ_371479,RMVar_hsa_circ_49806,RMVar_hsa_circ_336739,RMVar_hsa_circ_127500,RMVar_hsa_circ_151336,RMVar_hsa_circ_151337,RMVar_hsa_circ_317435,RMVar_hsa_circ_151338,RMVar_hsa_circ_151339,RMVar_hsa_circ_22886,RMVar_hsa_circ_77412,RMVar_hsa_circ_151340 3894 RMVar_ID_3894 Human_SNP_ID_471035757 A-to-I Human chr11 + 69091067 69091067 69091067 AGGGTCTTGCTCTGTTACCCAGGCTGGAGTGCAGTGGTGTGATCATGGCTCACTGCAGCCTCCAA AGGGTCTTGCTCTGTTACCCAGGCTGGAGTGCGGTGGTGTGATCATGGCTCACTGCAGCCTCCAA A G TPCN2,AP003071.5 Ensembl:ENSG00000162341,Ensembl:ENSG00000287725 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1236433044 Functional Loss SNV dbSNP153 33..33 33 - - - 3895 RMVar_ID_3895 Human_SNP_ID_471035765 A-to-I Human chr11 + 69091091 69091091 69091091 TGGAGTGCAGTGGTGTGATCATGGCTCACTGCAGCCTCCAACTTGTGGGCTCAAGCAGTCCTCCT TGGAGTGCAGTGGTGTGATCATGGCTCACTGCGGCCTCCAACTTGTGGGCTCAAGCAGTCCTCCT A G TPCN2,AP003071.5 Ensembl:ENSG00000162341,Ensembl:ENSG00000287725 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1377533258 Functional Loss SNV dbSNP153 33..33 33 - - - 3896 RMVar_ID_3896 Human_SNP_ID_471035784 A-to-I Human chr11 + 69091195 69091195 69091195 CACCAGGTCTGGCTAATTGTTTTATTTCTTGTAGAGATGGAGTATCTCTATGTTGCCCAGGCTAT CACCAGGTCTGGCTAATTGTTTTATTTCTTGTGGAGATGGAGTATCTCTATGTTGCCCAGGCTAT A G TPCN2,AP003071.5 Ensembl:ENSG00000162341,Ensembl:ENSG00000287725 Protein coding,Protein coding intron,intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1287517521 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11696738 3897 RMVar_ID_3897 Human_SNP_ID_471186338 A-to-I Human chr11 - 69665414 69665414 69665414 TGGGCCTTAGATTTCTGCCAGCTTGTCTCCTTAACCTAGCGTAGACACAGCCACTGCGAGAGTGC TGGGCCTTAGATTTCTGCCAGCTTGTCTCCTTCACCTAGCGTAGACACAGCCACTGCGAGAGTGC T G LTO1 Ensembl:ENSG00000149716 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1374346675 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48671,RMVar_hsa_circ_40424,RMVar_hsa_circ_151350 3898 RMVar_ID_3898 Human_SNP_ID_471186459 A-to-I Human chr11 - 69665892 69665892 69665892 CGTCCACCTACCAAAGTGCTGGAATTGCAGGCATGAGCCACCACTCCCGGCCTGCTTTTTGTTTT CGTCCACCTACCAAAGTGCTGGAATTGCAGGCGTGAGCCACCACTCCCGGCCTGCTTTTTGTTTT T C LTO1 Ensembl:ENSG00000149716 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1162000436 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48671,RMVar_hsa_circ_40424,RMVar_hsa_circ_151350 3899 RMVar_ID_3899 Human_SNP_ID_120208887 A-to-I Human chr3 - 2132221 2132221 2132221 ATGTCCAAGGTAATTTACATGTCTGGCACACTAGCTGGGAGAGCTAGAATAGCAGCTGGCTGGCC ATGTCCAAGGTAATTTACATGTCTGGCACACTGGCTGGGAGAGCTAGAATAGCAGCTGGCTGGCC T C CNTN4-AS2 Ensembl:ENSG00000227588 lincRNA intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs909065749 Functional Loss SNV dbSNP153 33..33 33 - - - 3900 RMVar_ID_3900 Human_SNP_ID_120515735 A-to-I Human chr3 - 3172497 3172497 3172497 GCATCTTTTAAAAATGATTTTCAGGTGATTCTAATGTCTCTCCAGGTTTGAGAACAATCATGTAA GCATCTTTTAAAAATGATTTTCAGGTGATTCTGATGTCTCTCCAGGTTTGAGAACAATCATGTAA T C CRBN Ensembl:ENSG00000113851 Protein coding intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs780978850 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1961136,Human_RBP_ID_19119259 RMVar_hsa_circ_60313,RMVar_hsa_circ_365596,RMVar_hsa_circ_304560,RMVar_hsa_circ_215457,RMVar_hsa_circ_34416,RMVar_hsa_circ_56046,RMVar_hsa_circ_215454,RMVar_hsa_circ_277307,RMVar_hsa_circ_40336,RMVar_hsa_circ_215455,RMVar_hsa_circ_30119,RMVar_hsa_circ_70441,RMVar_hsa_circ_324769,RMVar_hsa_circ_215456,RMVar_hsa_circ_278406,RMVar_hsa_circ_215458,RMVar_hsa_circ_215460,RMVar_hsa_circ_215462,RMVar_hsa_circ_279870,RMVar_hsa_circ_321327,RMVar_hsa_circ_299597,RMVar_hsa_circ_215463,RMVar_hsa_circ_215461 3901 RMVar_ID_3901 Human_SNP_ID_120710205 A-to-I Human chr3 + 3841612 3841612 3841612 GCCATCTTGGCTCACTGCAACCTCTGCCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGGCCCCTG GCCATCTTGGCTCACTGCAACCTCTGCCTCCCTGGTTCAAGCGATTCTCCTGCCTCAGGCCCCTG A T LRRN1 Ensembl:ENSG00000175928 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1013508298 Functional Loss SNV dbSNP153 33..33 33 - - - 3902 RMVar_ID_3902 Human_SNP_ID_120753448 A-to-I Human chr3 - 3983365 3983365 3983365 GATGAAGCTGTTAACAAAATAAGATTAGATACAGAGGAACAACTAAAAGAAATATTTCCAGAGGT GATGAAGCTGTTAACAAAATAAGATTAGATACGGAGGAACAACTAAAAGAAATATTTCCAGAGGT T C PNPT1P1,SUMF1 Ensembl:ENSG00000229241,Ensembl:ENSG00000144455 Pseudogene,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1399499778 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8264162,Human_RBP_ID_18536414 3903 RMVar_ID_3903 Human_SNP_ID_120753458 A-to-I Human chr3 - 3983406 3983406 3983406 ATGCAGTTTTTACAGATTATGAACATGATAAAATTTCCAGAGATGAAGCTGTTAACAAAATAAGA ATGCAGTTTTTACAGATTATGAACATGATAAAGTTTCCAGAGATGAAGCTGTTAACAAAATAAGA T C PNPT1P1,SUMF1 Ensembl:ENSG00000229241,Ensembl:ENSG00000144455 Pseudogene,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1169828253 Functional Loss SNV dbSNP153 33..33 33 - - - 3904 RMVar_ID_3904 Human_SNP_ID_120753463 A-to-I Human chr3 - 3983416 3983416 3983416 GAGAGACTCTATGCAGTTTTTACAGATTATGAACATGATAAAATTTCCAGAGATGAAGCTGTTAA GAGAGACTCTATGCAGTTTTTACAGATTATGAGCATGATAAAATTTCCAGAGATGAAGCTGTTAA T C PNPT1P1,SUMF1 Ensembl:ENSG00000229241,Ensembl:ENSG00000144455 Pseudogene,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1487990763 Functional Loss SNV dbSNP153 33..33 33 - - - 3905 RMVar_ID_3905 Human_SNP_ID_120839803 A-to-I Human chr3 - 4272889 4272889 4272889 TAAACTTTTCTGTAGAGATGCTGTCTGGCTATATTGCCCAGGTTGGTCTCAAACTCCTGGCCTCA TAAACTTTTCTGTAGAGATGCTGTCTGGCTATGTTGCCCAGGTTGGTCTCAAACTCCTGGCCTCA T C AC023483.1,SUMF1 Ensembl:ENSG00000286579,Ensembl:ENSG00000144455 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1291542323 Functional Loss SNV dbSNP153 33..33 33 - - - 3906 RMVar_ID_3906 Human_SNP_ID_120847584 A-to-I Human chr3 - 4300062 4300062 4300062 AACCCGCCCCCATGATCCAGTCTTCTCCTACTATGCCCCACCTCCAACACTGGGGATTAGATTTC AACCCGCCCCCATGATCCAGTCTTCTCCTACTGTGCCCCACCTCCAACACTGGGGATTAGATTTC T C AC023483.1,SUMF1 Ensembl:ENSG00000286579,Ensembl:ENSG00000144455 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1396943725 Functional Loss SNV dbSNP153 33..33 33 - - - 3907 RMVar_ID_3907 Human_SNP_ID_120887595 A-to-I Human chr3 - 4443271 4443271 4443271 ACCTCATTTTTTAAATTTTTATTTTTTGAGACAGAGTCTGGCTCTGTCACCAAGGCTAGAGTGCG ACCTCATTTTTTAAATTTTTATTTTTTGAGACGGAGTCTGGCTCTGTCACCAAGGCTAGAGTGCG T C SUMF1 Ensembl:ENSG00000144455 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs527864847 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83151,RMVar_hsa_circ_318999,RMVar_hsa_circ_84868,RMVar_hsa_circ_215491,RMVar_hsa_circ_215492,RMVar_hsa_circ_275080,RMVar_hsa_circ_280032,RMVar_hsa_circ_215494,RMVar_hsa_circ_376769,RMVar_hsa_circ_215493,RMVar_hsa_circ_215501 3908 RMVar_ID_3908 Human_SNP_ID_120915681 A-to-I Human chr3 + 4544806 4544806 4544806 TAGCTTTGCTTTCATTGCAACAACAACTTTTTATTTTTTAGACAGGGTCTTACTCTGTTGCCCAG TAGCTTTGCTTTCATTGCAACAACAACTTTTTGTTTTTTAGACAGGGTCTTACTCTGTTGCCCAG A G ITPR1 Ensembl:ENSG00000150995 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs914026272 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7199366,Human_RBP_ID_14835532 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 3909 RMVar_ID_3909 Human_SNP_ID_120915885 A-to-I Human chr3 + 4545548 4545546 4545548 AGGAGGCTGAGGTGTAAGGATCTCTGGACCCTAGGAGACTGAAGCTGAAGTGAGCCATGACTGTG AGGAGGCTGAGGTGTAAGGATCTCTGGACCC__GGAGACTGAAGCTGAAGTGAGCCATGACTGTG CTA C ITPR1 Ensembl:ENSG00000150995 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1324704800 Functional Loss DEL dbSNP153 32..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 3910 RMVar_ID_3910 Human_SNP_ID_120915907 A-to-I Human chr3 + 4545602 4545602 4545602 CCATGACTGTGCCACTGCACTGCAGCCTGGGCAACAGAACGGGACCCGGTCTCAAAAAAAAAAAA CCATGACTGTGCCACTGCACTGCAGCCTGGGCGACAGAACGGGACCCGGTCTCAAAAAAAAAAAA A G ITPR1 Ensembl:ENSG00000150995 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1252208364 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 3911 RMVar_ID_3911 Human_SNP_ID_120976049 A-to-I Human chr3 + 4756810 4756810 4756810 ACCAACTAGAATTATCACTGGATGCAAGTTGGACACTAGTCTTTGGCCATTTATGTAACACCCAG ACCAACTAGAATTATCACTGGATGCAAGTTGGGCACTAGTCTTTGGCCATTTATGTAACACCCAG A G ITPR1 Ensembl:ENSG00000150995 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251836631 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12198,RMVar_hsa_circ_330076,RMVar_hsa_circ_365117,RMVar_hsa_circ_356709,RMVar_hsa_circ_37013,RMVar_hsa_circ_14392,RMVar_hsa_circ_16043,RMVar_hsa_circ_319388,RMVar_hsa_circ_49957,RMVar_hsa_circ_267161,RMVar_hsa_circ_215527,RMVar_hsa_circ_301269,RMVar_hsa_circ_309301,RMVar_hsa_circ_39043,RMVar_hsa_circ_215528,RMVar_hsa_circ_215530,RMVar_hsa_circ_215529 3912 RMVar_ID_3912 Human_SNP_ID_120976085 A-to-I Human chr3 + 4756942 4756941 4756943 ACCTTCCATCTGAGTAGTTCTTGGTAGTAATCAAAGTGTTTTTCACACCTACTGTTTCATAACAA ACCTTCCATCTGAGTAGTTCTTGGTAGTAATC__AGTGTTTTTCACACCTACTGTTTCATAACAA CAA C ITPR1 Ensembl:ENSG00000150995 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1214076912 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_12198,RMVar_hsa_circ_330076,RMVar_hsa_circ_365117,RMVar_hsa_circ_356709,RMVar_hsa_circ_37013,RMVar_hsa_circ_14392,RMVar_hsa_circ_16043,RMVar_hsa_circ_319388,RMVar_hsa_circ_49957,RMVar_hsa_circ_267161,RMVar_hsa_circ_215527,RMVar_hsa_circ_301269,RMVar_hsa_circ_309301,RMVar_hsa_circ_39043,RMVar_hsa_circ_215528,RMVar_hsa_circ_215530,RMVar_hsa_circ_215529 3913 RMVar_ID_3913 Human_SNP_ID_120976085 A-to-I Human chr3 + 4756943 4756941 4756943 CCTTCCATCTGAGTAGTTCTTGGTAGTAATCAAAGTGTTTTTCACACCTACTGTTTCATAACAAC CCTTCCATCTGAGTAGTTCTTGGTAGTAATC__AGTGTTTTTCACACCTACTGTTTCATAACAAC CAA C ITPR1 Ensembl:ENSG00000150995 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1214076912 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_12198,RMVar_hsa_circ_330076,RMVar_hsa_circ_365117,RMVar_hsa_circ_356709,RMVar_hsa_circ_37013,RMVar_hsa_circ_14392,RMVar_hsa_circ_16043,RMVar_hsa_circ_319388,RMVar_hsa_circ_49957,RMVar_hsa_circ_267161,RMVar_hsa_circ_215527,RMVar_hsa_circ_301269,RMVar_hsa_circ_309301,RMVar_hsa_circ_39043,RMVar_hsa_circ_215528,RMVar_hsa_circ_215530,RMVar_hsa_circ_215529 3914 RMVar_ID_3914 Human_SNP_ID_120977297 A-to-I Human chr3 + 4761384 4761384 4761384 AAATGTAGTATTTGGTTTTCTGCTCCTGCATCAATTTGCTTAGGAAAATGACCCCCAGCTGCATC AAATGTAGTATTTGGTTTTCTGCTCCTGCATCCATTTGCTTAGGAAAATGACCCCCAGCTGCATC A C ITPR1 Ensembl:ENSG00000150995 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs959754445 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12198,RMVar_hsa_circ_330076,RMVar_hsa_circ_365117,RMVar_hsa_circ_356709,RMVar_hsa_circ_37013,RMVar_hsa_circ_14392,RMVar_hsa_circ_16043,RMVar_hsa_circ_319388,RMVar_hsa_circ_49957,RMVar_hsa_circ_267161,RMVar_hsa_circ_215527,RMVar_hsa_circ_301269,RMVar_hsa_circ_309301,RMVar_hsa_circ_39043,RMVar_hsa_circ_215528,RMVar_hsa_circ_215530,RMVar_hsa_circ_215529 3915 RMVar_ID_3915 Human_SNP_ID_120977298 A-to-I Human chr3 + 4761384 4761384 4761384 AAATGTAGTATTTGGTTTTCTGCTCCTGCATCAATTTGCTTAGGAAAATGACCCCCAGCTGCATC AAATGTAGTATTTGGTTTTCTGCTCCTGCATCGATTTGCTTAGGAAAATGACCCCCAGCTGCATC A G ITPR1 Ensembl:ENSG00000150995 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs959754445 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12198,RMVar_hsa_circ_330076,RMVar_hsa_circ_365117,RMVar_hsa_circ_356709,RMVar_hsa_circ_37013,RMVar_hsa_circ_14392,RMVar_hsa_circ_16043,RMVar_hsa_circ_319388,RMVar_hsa_circ_49957,RMVar_hsa_circ_267161,RMVar_hsa_circ_215527,RMVar_hsa_circ_301269,RMVar_hsa_circ_309301,RMVar_hsa_circ_39043,RMVar_hsa_circ_215528,RMVar_hsa_circ_215530,RMVar_hsa_circ_215529 3916 RMVar_ID_3916 Human_SNP_ID_120977711 A-to-I Human chr3 + 4762976 4762976 4762976 CCCATCAATGATAGACTGGATAAAGAAATTATAGTACATAAACTATGCAGCCATAAAATGTGGAA CCCATCAATGATAGACTGGATAAAGAAATTATGGTACATAAACTATGCAGCCATAAAATGTGGAA A G ITPR1 Ensembl:ENSG00000150995 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs775956708 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12198,RMVar_hsa_circ_330076,RMVar_hsa_circ_365117,RMVar_hsa_circ_356709,RMVar_hsa_circ_37013,RMVar_hsa_circ_14392,RMVar_hsa_circ_16043,RMVar_hsa_circ_319388,RMVar_hsa_circ_49957,RMVar_hsa_circ_267161,RMVar_hsa_circ_215527,RMVar_hsa_circ_301269,RMVar_hsa_circ_309301,RMVar_hsa_circ_39043,RMVar_hsa_circ_215528,RMVar_hsa_circ_215530,RMVar_hsa_circ_215529 3917 RMVar_ID_3917 Human_SNP_ID_120977747 A-to-I Human chr3 + 4763149 4763149 4763149 CACATGTTCTCATTTACAAGTATGAGCTGAACAATGAGAACACATGGACACAGGGAGGGGAACAA CACATGTTCTCATTTACAAGTATGAGCTGAACGATGAGAACACATGGACACAGGGAGGGGAACAA A G ITPR1 Ensembl:ENSG00000150995 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1282699341 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12198,RMVar_hsa_circ_330076,RMVar_hsa_circ_365117,RMVar_hsa_circ_356709,RMVar_hsa_circ_37013,RMVar_hsa_circ_14392,RMVar_hsa_circ_16043,RMVar_hsa_circ_319388,RMVar_hsa_circ_49957,RMVar_hsa_circ_267161,RMVar_hsa_circ_215527,RMVar_hsa_circ_301269,RMVar_hsa_circ_309301,RMVar_hsa_circ_39043,RMVar_hsa_circ_215528,RMVar_hsa_circ_215530,RMVar_hsa_circ_215529 3918 RMVar_ID_3918 Human_SNP_ID_121041549 A-to-I Human chr3 - 4992620 4992620 4992620 AACTTCTTGGCTGTGCATGGTGGCTCGGGCCTATAATCCCAGCACTTTGGGAGGCCAAGACAAGA AACTTCTTGGCTGTGCATGGTGGCTCGGGCCTGTAATCCCAGCACTTTGGGAGGCCAAGACAAGA T C lnc-SUMF1-12,lnc-SUMF1-12:2,lnc-SUMF1-12:3,lnc-SUMF1-12:4 RNACentral:URS00009BB2CF,RNACentral:URS00009B9C39,RNACentral:URS00009AEAAC,RNACentral:URS0000D5E360 lincRNA,lincRNA,lincRNA,lincRNA exon,intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560895372 Functional Loss SNV dbSNP153 33..33 33 - - - 3919 RMVar_ID_3919 Human_SNP_ID_121083696 A-to-I Human chr3 + 5128114 5128114 5128114 GAACCTGGGAGGCGGAGGTTGCGTTGAGCCGAAATTGAGCGACTGCACTCCAGCCTGGGCAACAG GAACCTGGGAGGCGGAGGTTGCGTTGAGCCGACATTGAGCGACTGCACTCCAGCCTGGGCAACAG A C ARL8B Ensembl:ENSG00000134108 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1174158654 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14884176,Human_RBP_ID_25744821 3920 RMVar_ID_3920 Human_SNP_ID_121084397 A-to-I Human chr3 + 5130207 5130207 5130207 CTCTTAAAAAAAAATATATATTTTTTTTTTGTAGAGACTTCATCTCACTGTGTTGCTCAGCCTGG CTCTTAAAAAAAAATATATATTTTTTTTTTGTTGAGACTTCATCTCACTGTGTTGCTCAGCCTGG A T ARL8B Ensembl:ENSG00000134108 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1261723853 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14884707 3921 RMVar_ID_3921 Human_SNP_ID_121084821 A-to-I Human chr3 + 5131414 5131413 5131415 AAAAATTAAAAAATTTTTTTTTTTTTTGAGACAGAGTCTCACTCTGTCACCCAGGCTGGAGTGCA AAAAATTAAAAAATTTTTTTTTTTTTTGAGAC__AGTCTCACTCTGTCACCCAGGCTGGAGTGCA CAG C ARL8B Ensembl:ENSG00000134108 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459310856 Functional Loss DEL dbSNP153 33..34 33 - - - 3922 RMVar_ID_3922 Human_SNP_ID_121084822 A-to-I Human chr3 + 5131414 5131414 5131414 AAAAATTAAAAAATTTTTTTTTTTTTTGAGACAGAGTCTCACTCTGTCACCCAGGCTGGAGTGCA AAAAATTAAAAAATTTTTTTTTTTTTTGAGACGGAGTCTCACTCTGTCACCCAGGCTGGAGTGCA A G ARL8B Ensembl:ENSG00000134108 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1344320224 Functional Loss SNV dbSNP153 33..33 33 - - - 3923 RMVar_ID_3923 Human_SNP_ID_121503444 A-to-I Human chr3 + 6515325 6515325 6515325 TCACGCCATTCTCCTGCCTCAGCCTCCCTAGTAGCTGAGACTCCAGGTGCCCGCCACCATGCCCG TCACGCCATTCTCCTGCCTCAGCCTCCCTAGTGGCTGAGACTCCAGGTGCCCGCCACCATGCCCG A G AC069277.1 Ensembl:ENSG00000189229 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1385449770 Functional Loss SNV dbSNP153 33..33 33 - - - 3924 RMVar_ID_3924 Human_SNP_ID_121517621 A-to-I Human chr3 + 6564988 6564987 6564988 TCCTGGCTAACCGGTGAAATCCCGTCTCTACTAAAAATACAAAAAATTAGCCGGGTGCGGTGGCG TCCTGGCTAACCGGTGAAATCCCGTCTCTACT_AAAATACAAAAAATTAGCCGGGTGCGGTGGCG TA T AC069277.1 Ensembl:ENSG00000189229 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs781674981 Functional Loss DEL dbSNP153 33..33 33 - - - 3925 RMVar_ID_3925 Human_SNP_ID_121520677 A-to-I Human chr3 + 6575537 6575537 6575537 ATCACACCTGGCTAACTTTTTAATTTTTTTGTAGAGATAGGGTTTCACTATGTTGCCCAGGCTGG ATCACACCTGGCTAACTTTTTAATTTTTTTGTGGAGATAGGGTTTCACTATGTTGCCCAGGCTGG A G AC069277.1 Ensembl:ENSG00000189229 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1313695049 Functional Loss SNV dbSNP153 33..33 33 - - - 3926 RMVar_ID_3926 Human_SNP_ID_121520898 A-to-I Human chr3 + 6576270 6576270 6576270 AAAATTAGCTGGGCATGGTGGTGCAAGCCTTTAGTCCCAGCTACTGGGAAAGCTGAGATGGGAGA AAAATTAGCTGGGCATGGTGGTGCAAGCCTTTCGTCCCAGCTACTGGGAAAGCTGAGATGGGAGA A C AC069277.1 Ensembl:ENSG00000189229 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1390368520 Functional Loss SNV dbSNP153 33..33 33 - - - 3927 RMVar_ID_3927 Human_SNP_ID_121520899 A-to-I Human chr3 + 6576270 6576270 6576270 AAAATTAGCTGGGCATGGTGGTGCAAGCCTTTAGTCCCAGCTACTGGGAAAGCTGAGATGGGAGA AAAATTAGCTGGGCATGGTGGTGCAAGCCTTTGGTCCCAGCTACTGGGAAAGCTGAGATGGGAGA A G AC069277.1 Ensembl:ENSG00000189229 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1390368520 Functional Loss SNV dbSNP153 33..33 33 - - - 3928 RMVar_ID_3928 Human_SNP_ID_121543377 A-to-I Human chr3 + 6653850 6653850 6653850 AAAGTAGTGCATTATTTCACTGTCACATAGCTATAAAGAACTACCTGAGACTGGGTAACTTACAA AAAGTAGTGCATTATTTCACTGTCACATAGCTGTAAAGAACTACCTGAGACTGGGTAACTTACAA A G AC069277.1 Ensembl:ENSG00000189229 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1559215171 Functional Loss SNV dbSNP153 33..33 33 - - - 3929 RMVar_ID_3929 Human_SNP_ID_121543379 A-to-I Human chr3 + 6653852 6653852 6653852 AGTAGTGCATTATTTCACTGTCACATAGCTATAAAGAACTACCTGAGACTGGGTAACTTACAAAT AGTAGTGCATTATTTCACTGTCACATAGCTATGAAGAACTACCTGAGACTGGGTAACTTACAAAT A G AC069277.1 Ensembl:ENSG00000189229 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1437939198 Functional Loss SNV dbSNP153 33..33 33 - - - 3930 RMVar_ID_3930 Human_SNP_ID_121545651 A-to-I Human chr3 + 6662011 6662011 6662011 CACTAGGCTGTGCCCCAGTAGGGACTCTGTATAGTGGTTCTGACCCCACATTTCCCTTCCGGACT CACTAGGCTGTGCCCCAGTAGGGACTCTGTATGGTGGTTCTGACCCCACATTTCCCTTCCGGACT A G AC069277.1 Ensembl:ENSG00000189229 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1437093709 Functional Loss SNV dbSNP153 33..33 33 - - - 3931 RMVar_ID_3931 Human_SNP_ID_121547218 A-to-I Human chr3 + 6667639 6667639 6667639 TCCATCCGGCCTCTCTGGCTCCAGCCTAGCTTAAAGGGACCTGGGTACAACCTGGGCTACAGCGC TCCATCCGGCCTCTCTGGCTCCAGCCTAGCTTGAAGGGACCTGGGTACAACCTGGGCTACAGCGC A G AC069277.1 Ensembl:ENSG00000189229 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965044819 Functional Loss SNV dbSNP153 33..33 33 - - - 3932 RMVar_ID_3932 Human_SNP_ID_121547413 A-to-I Human chr3 + 6668263 6668263 6668263 CCTTTTGGAATGGCAGTGTTTATCTAATGCCTATACTTCCATTGGATCTTGGAAATAAGCAACTT CCTTTTGGAATGGCAGTGTTTATCTAATGCCTGTACTTCCATTGGATCTTGGAAATAAGCAACTT A G AC069277.1 Ensembl:ENSG00000189229 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1240124243 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17573988 3933 RMVar_ID_3933 Human_SNP_ID_121569074 A-to-I Human chr3 + 6738378 6738378 6738378 TTGGTTCACTGCAAACTCCGCCTCCTGGGTTCAAGCCTTTCTCCTGTCTCAGGCTCCCAAGTAGC TTGGTTCACTGCAAACTCCGCCTCCTGGGTTCCAGCCTTTCTCCTGTCTCAGGCTCCCAAGTAGC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs758174412 Functional Loss SNV dbSNP153 33..33 33 - - - 3934 RMVar_ID_3934 Human_SNP_ID_121620910 A-to-I Human chr3 + 6923249 6923249 6923249 GTTGGCCAGGCTGGTCTCGGACTTCTGACCTCAGATGATCCACCTGCCTCGGTCTCCCAAACTGC GTTGGCCAGGCTGGTCTCGGACTTCTGACCTCTGATGATCCACCTGCCTCGGTCTCCCAAACTGC A T GRM7 Ensembl:ENSG00000196277 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs548466095 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93596,RMVar_hsa_circ_215564 3935 RMVar_ID_3935 Human_SNP_ID_122275053 A-to-I Human chr3 - 9385135 9385135 9385135 AGCTCTGCTTTCTTATAAAATCTTTTTGAGACAGAGTTTCGCTCTTGTCGCACAGGCTGGAGTGC AGCTCTGCTTTCTTATAAAATCTTTTTGAGACGGAGTTTCGCTCTTGTCGCACAGGCTGGAGTGC T C THUMPD3-AS1 Ensembl:ENSG00000206573 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1012368860 Functional Loss SNV dbSNP153 33..33 33 - - - 3936 RMVar_ID_3936 Human_SNP_ID_122276374 A-to-I Human chr3 - 9389551 9389550 9389552 GCCCTGAGTGATCTTGCTTTGGGCCTCTCAAAATGTTGAGTTAATAGGCGTGAGCCACCATACCC GCCCTGAGTGATCTTGCTTTGGGCCTCTCAA__TGTTGAGTTAATAGGCGTGAGCCACCATACCC ATT A THUMPD3-AS1 Ensembl:ENSG00000206573 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1461903182 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_14961209,Human_RBP_ID_25772597 RMVar_hsa_circ_31666 3937 RMVar_ID_3937 Human_SNP_ID_122276406 A-to-I Human chr3 - 9389681 9389681 9389681 CTTCTGCCTCAGCCTCCTGAGTAGCTGGAACTATAGGCATGCGCCACCAAGCCTGGGCTTTTAAA CTTCTGCCTCAGCCTCCTGAGTAGCTGGAACTGTAGGCATGCGCCACCAAGCCTGGGCTTTTAAA T C THUMPD3-AS1 Ensembl:ENSG00000206573 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs561437118 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7250207,Human_RBP_ID_25759770 RMVar_hsa_circ_31666 3938 RMVar_ID_3938 Human_SNP_ID_122276470 A-to-I Human chr3 - 9389883 9389882 9389883 TGATTTGGAAGGACTGACTCAAACTAACGAAAATATGAAACCTGTCTTTCTGCTTTGGAGATATT TGATTTGGAAGGACTGACTCAAACTAACGAAA_TATGAAACCTGTCTTTCTGCTTTGGAGATATT AT A THUMPD3-AS1 Ensembl:ENSG00000206573 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs917186351 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_1632340,Human_RBP_ID_2802807,Human_RBP_ID_3719582,Human_RBP_ID_8580237,Human_RBP_ID_21939019,Human_RBP_ID_23025772,Human_RBP_ID_25772598 RMVar_hsa_circ_31666 3939 RMVar_ID_3939 Human_SNP_ID_122276471 A-to-I Human chr3 - 9389883 9389883 9389883 TGATTTGGAAGGACTGACTCAAACTAACGAAAATATGAAACCTGTCTTTCTGCTTTGGAGATATT TGATTTGGAAGGACTGACTCAAACTAACGAAAGTATGAAACCTGTCTTTCTGCTTTGGAGATATT T C THUMPD3-AS1 Ensembl:ENSG00000206573 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1401465755 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1632340,Human_RBP_ID_2802807,Human_RBP_ID_3719582,Human_RBP_ID_8580237,Human_RBP_ID_21939019,Human_RBP_ID_23025772,Human_RBP_ID_25772598 RMVar_hsa_circ_31666 3940 RMVar_ID_3940 Human_SNP_ID_122278150 A-to-I Human chr3 - 9395512 9395512 9395512 GTGATCTTGACTACTGCTTTACAGAGAATTGGATCTGAGGTTAGGCAACATCTCCCTTTTTCTTC GTGATCTTGACTACTGCTTTACAGAGAATTGGGTCTGAGGTTAGGCAACATCTCCCTTTTTCTTC T C THUMPD3-AS1 Ensembl:ENSG00000206573 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1389249569 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5606824,Human_RBP_ID_8211268,Human_RBP_ID_14961470,Human_RBP_ID_20960716 Human_Splice_Rec_389082,Human_Splice_Rec_389083,Human_Splice_Rec_389117,Human_Splice_Rec_389130,Human_Splice_Rec_389131,Human_Splice_Rec_389174,Human_Splice_Rec_389175,Human_Splice_Rec_389192,Human_Splice_Rec_389193 3941 RMVar_ID_3941 Human_SNP_ID_122285354 A-to-I Human chr3 + 9418968 9418968 9418968 CCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGTGTCCACCACTATGCCTGGCTGATTTTTGT CCTGCCTCAGCCTCCCAAGTAGCTGGGATTACGGGTGTCCACCACTATGCCTGGCTGATTTTTGT A G SETD5 Ensembl:ENSG00000168137 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1233494530 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_215635,RMVar_hsa_circ_119323,RMVar_hsa_circ_103294,RMVar_hsa_circ_215634 3942 RMVar_ID_3942 Human_SNP_ID_122292754 A-to-I Human chr3 + 9446090 9446090 9446090 TGGGCGGATCACGAGGTCAGGAGATCGAGACCATCCTCGCTAACACGGTGAAACCTTGTCTCTAC TGGGCGGATCACGAGGTCAGGAGATCGAGACCGTCCTCGCTAACACGGTGAAACCTTGTCTCTAC A G SETD5 Ensembl:ENSG00000168137 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1330993459 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_155776 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_85055,RMVar_hsa_circ_353233,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_332102,RMVar_hsa_circ_72505,RMVar_hsa_circ_215658,RMVar_hsa_circ_62211,RMVar_hsa_circ_3713,RMVar_hsa_circ_64880,RMVar_hsa_circ_43807,RMVar_hsa_circ_346618,RMVar_hsa_circ_215663,RMVar_hsa_circ_302892,RMVar_hsa_circ_359261,RMVar_hsa_circ_61019,RMVar_hsa_circ_65634,RMVar_hsa_circ_22491 3943 RMVar_ID_3943 Human_SNP_ID_122292766 A-to-I Human chr3 + 9446130 9446130 9446130 TAACACGGTGAAACCTTGTCTCTACTAAAAATACAAAAAATTAGCCGGGCGCGGTGGCGGGTGCC TAACACGGTGAAACCTTGTCTCTACTAAAAATCCAAAAAATTAGCCGGGCGCGGTGGCGGGTGCC A C SETD5 Ensembl:ENSG00000168137 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1400357579 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_155776 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_85055,RMVar_hsa_circ_353233,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_332102,RMVar_hsa_circ_72505,RMVar_hsa_circ_215658,RMVar_hsa_circ_62211,RMVar_hsa_circ_3713,RMVar_hsa_circ_64880,RMVar_hsa_circ_43807,RMVar_hsa_circ_346618,RMVar_hsa_circ_215663,RMVar_hsa_circ_302892,RMVar_hsa_circ_359261,RMVar_hsa_circ_61019,RMVar_hsa_circ_65634,RMVar_hsa_circ_22491 3944 RMVar_ID_3944 Human_SNP_ID_122292944 A-to-I Human chr3 + 9446592 9446592 9446592 TCAACTCACCACAATCTCTGCCTCCCGGGTTCAAGCAATTCCCCTTCCTTAGCCTCCCAAGTAGC TCAACTCACCACAATCTCTGCCTCCCGGGTTCTAGCAATTCCCCTTCCTTAGCCTCCCAAGTAGC A T SETD5 Ensembl:ENSG00000168137 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs944967305 Functional Loss SNV dbSNP153 33..33 33 - - - 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_85055,RMVar_hsa_circ_353233,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_332102,RMVar_hsa_circ_72505,RMVar_hsa_circ_215658,RMVar_hsa_circ_62211,RMVar_hsa_circ_3713,RMVar_hsa_circ_64880,RMVar_hsa_circ_43807,RMVar_hsa_circ_346618,RMVar_hsa_circ_215663,RMVar_hsa_circ_302892,RMVar_hsa_circ_359261,RMVar_hsa_circ_61019,RMVar_hsa_circ_65634,RMVar_hsa_circ_22491 3945 RMVar_ID_3945 Human_SNP_ID_122292975 A-to-I Human chr3 + 9446693 9446693 9446693 TTTTTGTATTTTAGTAGAGACGGAGTTTCACCATGTTGGCCACGACGGTCTCAATCTCCCGACCT TTTTTGTATTTTAGTAGAGACGGAGTTTCACCCTGTTGGCCACGACGGTCTCAATCTCCCGACCT A C SETD5 Ensembl:ENSG00000168137 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs544464719 Functional Loss SNV dbSNP153 33..33 33 - - - 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_85055,RMVar_hsa_circ_353233,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_332102,RMVar_hsa_circ_72505,RMVar_hsa_circ_215658,RMVar_hsa_circ_62211,RMVar_hsa_circ_3713,RMVar_hsa_circ_64880,RMVar_hsa_circ_43807,RMVar_hsa_circ_346618,RMVar_hsa_circ_215663,RMVar_hsa_circ_302892,RMVar_hsa_circ_359261,RMVar_hsa_circ_61019,RMVar_hsa_circ_65634,RMVar_hsa_circ_22491 3946 RMVar_ID_3946 Human_SNP_ID_122297716 A-to-I Human chr3 + 9463138 9463138 9463138 GCCTCCTGGGTTCAAGTGATTCTTGTGCCTCCACCTCCTGAGTAACTGGAACTGCAGGCATGCAC GCCTCCTGGGTTCAAGTGATTCTTGTGCCTCCCCCTCCTGAGTAACTGGAACTGCAGGCATGCAC A C SETD5 Ensembl:ENSG00000168137 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs934666678 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_301307,RMVar_hsa_circ_329981,RMVar_hsa_circ_44841,RMVar_hsa_circ_315370,RMVar_hsa_circ_13045,RMVar_hsa_circ_353608,RMVar_hsa_circ_62908,RMVar_hsa_circ_55533,RMVar_hsa_circ_85055,RMVar_hsa_circ_353233,RMVar_hsa_circ_374649,RMVar_hsa_circ_121045,RMVar_hsa_circ_215654,RMVar_hsa_circ_215656,RMVar_hsa_circ_215655,RMVar_hsa_circ_332102,RMVar_hsa_circ_215658,RMVar_hsa_circ_62211,RMVar_hsa_circ_3713,RMVar_hsa_circ_43807,RMVar_hsa_circ_307934,RMVar_hsa_circ_60549,RMVar_hsa_circ_215666,RMVar_hsa_circ_74772,RMVar_hsa_circ_118676,RMVar_hsa_circ_299200,RMVar_hsa_circ_114369,RMVar_hsa_circ_215664,RMVar_hsa_circ_215665 3947 RMVar_ID_3947 Human_SNP_ID_122297728 A-to-I Human chr3 + 9463212 9463212 9463212 TGCTTAATCTTTTTTGTGTATTTAGTAGAGACAGGGTTTTGCCATATTGGCCAGGCTGGTCTCAA TGCTTAATCTTTTTTGTGTATTTAGTAGAGACGGGGTTTTGCCATATTGGCCAGGCTGGTCTCAA A G SETD5 Ensembl:ENSG00000168137 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1265860814 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_301307,RMVar_hsa_circ_329981,RMVar_hsa_circ_44841,RMVar_hsa_circ_315370,RMVar_hsa_circ_13045,RMVar_hsa_circ_353608,RMVar_hsa_circ_62908,RMVar_hsa_circ_55533,RMVar_hsa_circ_85055,RMVar_hsa_circ_353233,RMVar_hsa_circ_374649,RMVar_hsa_circ_121045,RMVar_hsa_circ_215654,RMVar_hsa_circ_215656,RMVar_hsa_circ_215655,RMVar_hsa_circ_332102,RMVar_hsa_circ_215658,RMVar_hsa_circ_62211,RMVar_hsa_circ_3713,RMVar_hsa_circ_43807,RMVar_hsa_circ_307934,RMVar_hsa_circ_60549,RMVar_hsa_circ_215666,RMVar_hsa_circ_74772,RMVar_hsa_circ_118676,RMVar_hsa_circ_299200,RMVar_hsa_circ_114369,RMVar_hsa_circ_215664,RMVar_hsa_circ_215665 3948 RMVar_ID_3948 Human_SNP_ID_122301606 A-to-I Human chr3 + 9476477 9476477 9476477 CATCTTTTTAAATTTAAAAAAAAAAAAAAAAAAAGTTTTCAAAGGAAAAAAAGTTAAAAGAGCCA CATCTTTTTAAATTTAAAAAAAAAAAAAAAAAGAGTTTTCAAAGGAAAAAAAGTTAAAAGAGCCA A G SETD5 Ensembl:ENSG00000168137 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1038860329 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_609069,Human_RBP_ID_27059951 RMVar_hsa_circ_112912,RMVar_hsa_circ_215670 3949 RMVar_ID_3949 Human_SNP_ID_122308255 A-to-I Human chr3 - 9500482 9500482 9500482 TGGACCCTAGCCGGAATCAGATGTTGGGACCTAGTGGGTTCCTGCCACCTGGAACTTACCAAGTC TGGACCCTAGCCGGAATCAGATGTTGGGACCTCGTGGGTTCCTGCCACCTGGAACTTACCAAGTC T G LHFPL4 Ensembl:ENSG00000156959 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1309296560 Functional Loss SNV dbSNP153 33..33 33 - - - 3950 RMVar_ID_3950 Human_SNP_ID_122333243 A-to-I Human chr3 - 9588767 9588767 9588767 AAAATTAGCCGGGCATGGTGGCGGGAGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTAGCCGGGCATGGTGGCGGGAGCCTGTCGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1290834240 Functional Loss SNV dbSNP153 33..33 33 - - - 3951 RMVar_ID_3951 Human_SNP_ID_122350814 A-to-I Human chr3 + 9650973 9650973 9650973 ACCACGCCCAGCTAATTATTGTAGTTTTTAGTAGAGATGGAGTTTCCCCAGGTTGGCCAGGCTGG ACCACGCCCAGCTAATTATTGTAGTTTTTAGTTGAGATGGAGTTTCCCCAGGTTGGCCAGGCTGG A T MTMR14 Ensembl:ENSG00000163719 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1209502224 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84423,RMVar_hsa_circ_215672 3952 RMVar_ID_3952 Human_SNP_ID_122350920 A-to-I Human chr3 + 9651355 9651355 9651355 AAACTCCTAAGCTCAAGCAATCCTCCCACCTCAGCCCCCCAAAATGCTGGGATTACAGGCGTGAG AAACTCCTAAGCTCAAGCAATCCTCCCACCTCCGCCCCCCAAAATGCTGGGATTACAGGCGTGAG A C MTMR14 Ensembl:ENSG00000163719 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs926069472 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84423,RMVar_hsa_circ_215672 3953 RMVar_ID_3953 Human_SNP_ID_122352255 A-to-I Human chr3 + 9656011 9656011 9656011 GAGGTCAGGAGATTGAGACCATCCTGGCCAACATGGTGAAACCCCGTATCTACTAAATATACAAA GAGGTCAGGAGATTGAGACCATCCTGGCCAACGTGGTGAAACCCCGTATCTACTAAATATACAAA A G MTMR14 Ensembl:ENSG00000163719 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs748674667 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84423,RMVar_hsa_circ_115827,RMVar_hsa_circ_215672,RMVar_hsa_circ_322734,RMVar_hsa_circ_215673 3954 RMVar_ID_3954 Human_SNP_ID_122353028 A-to-I Human chr3 + 9658916 9658916 9658916 TTCTTCTGTATTTGAAAATAGTTTGGCTGGGCATGGTGGCTCACGCCTATAATCCTAGTTACTTG TTCTTCTGTATTTGAAAATAGTTTGGCTGGGCGTGGTGGCTCACGCCTATAATCCTAGTTACTTG A G MTMR14 Ensembl:ENSG00000163719 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs979279284 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84423,RMVar_hsa_circ_115827,RMVar_hsa_circ_215672,RMVar_hsa_circ_322734,RMVar_hsa_circ_215673 3955 RMVar_ID_3955 Human_SNP_ID_122353069 A-to-I Human chr3 + 9659092 9659092 9659092 CTTGTCACTACAAAAAATACAAAGCATTAGCCAAGCATCGTGGCATGTGCCTGTAGTCCCAGCTA CTTGTCACTACAAAAAATACAAAGCATTAGCCCAGCATCGTGGCATGTGCCTGTAGTCCCAGCTA A C MTMR14 Ensembl:ENSG00000163719 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs919304746 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84423,RMVar_hsa_circ_115827,RMVar_hsa_circ_215672,RMVar_hsa_circ_322734,RMVar_hsa_circ_215673 3956 RMVar_ID_3956 Human_SNP_ID_122353454 A-to-I Human chr3 + 9660358 9660358 9660358 TTGGCTCACTGCAAACTCTGCCTCCCGGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCTGAGTAGC TTGGCTCACTGCAAACTCTGCCTCCCGGGTTCCAGCAGTTCTCCTGCCTCAGCCTCCTGAGTAGC A C MTMR14 Ensembl:ENSG00000163719 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1341415869 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84423,RMVar_hsa_circ_115827,RMVar_hsa_circ_215672,RMVar_hsa_circ_322734,RMVar_hsa_circ_215673 3957 RMVar_ID_3957 Human_SNP_ID_122353455 A-to-I Human chr3 + 9660362 9660362 9660362 CTCACTGCAAACTCTGCCTCCCGGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCTGAGTAGCTGGG CTCACTGCAAACTCTGCCTCCCGGGTTCAAGCGGTTCTCCTGCCTCAGCCTCCTGAGTAGCTGGG A G MTMR14 Ensembl:ENSG00000163719 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1326374657 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84423,RMVar_hsa_circ_115827,RMVar_hsa_circ_215672,RMVar_hsa_circ_322734,RMVar_hsa_circ_215673 3958 RMVar_ID_3958 Human_SNP_ID_122353456 A-to-I Human chr3 + 9660362 9660362 9660362 CTCACTGCAAACTCTGCCTCCCGGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCTGAGTAGCTGGG CTCACTGCAAACTCTGCCTCCCGGGTTCAAGCTGTTCTCCTGCCTCAGCCTCCTGAGTAGCTGGG A T MTMR14 Ensembl:ENSG00000163719 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1326374657 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84423,RMVar_hsa_circ_115827,RMVar_hsa_circ_215672,RMVar_hsa_circ_322734,RMVar_hsa_circ_215673 3959 RMVar_ID_3959 Human_SNP_ID_122353872 A-to-I Human chr3 + 9661944 9661944 9661944 CCCCGTCTCTACCAAAAATAAAAAAATTACCCAGGTGTGGTGGCTCACACCTGTAGTCACAGCAT CCCCGTCTCTACCAAAAATAAAAAAATTACCCGGGTGTGGTGGCTCACACCTGTAGTCACAGCAT A G MTMR14 Ensembl:ENSG00000163719 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1378112315 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84423,RMVar_hsa_circ_115827,RMVar_hsa_circ_215672,RMVar_hsa_circ_322734,RMVar_hsa_circ_215673 3960 RMVar_ID_3960 Human_SNP_ID_122355169 A-to-I Human chr3 + 9666227 9666227 9666227 GCCATCTTGGCTCACTGTAACCTCTGCCTCCCAGGCTCTAGCGATTCTTGTGCCTCAGCCTCCCA GCCATCTTGGCTCACTGTAACCTCTGCCTCCCGGGCTCTAGCGATTCTTGTGCCTCAGCCTCCCA A G MTMR14 Ensembl:ENSG00000163719 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs902347098 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23886,RMVar_hsa_circ_115827,RMVar_hsa_circ_358221,RMVar_hsa_circ_215673,RMVar_hsa_circ_284552,RMVar_hsa_circ_215674 3961 RMVar_ID_3961 Human_SNP_ID_122364567 A-to-I Human chr3 + 9700991 9700991 9700991 CAGGCATATGCCACCATGTCCAGTGAATTTTTATATTTTCAGTAGAGACAGGGTTTTGCCATGTT CAGGCATATGCCACCATGTCCAGTGAATTTTTGTATTTTCAGTAGAGACAGGGTTTTGCCATGTT A G MTMR14 Ensembl:ENSG00000163719 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1317354604 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115827,RMVar_hsa_circ_215673,RMVar_hsa_circ_377401,RMVar_hsa_circ_215684,RMVar_hsa_circ_215683 3962 RMVar_ID_3962 Human_SNP_ID_122364674 A-to-I Human chr3 + 9701430 9701430 9701430 TGGTGGCATGTGCCTGTAGTCCCAGCTACTTGAGGGGCTGAGGTGGGAGGATGGCTTGAGGCTAC TGGTGGCATGTGCCTGTAGTCCCAGCTACTTGGGGGGCTGAGGTGGGAGGATGGCTTGAGGCTAC A G MTMR14 Ensembl:ENSG00000163719 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1243222518 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22605053 RMVar_hsa_circ_115827,RMVar_hsa_circ_215673,RMVar_hsa_circ_377401,RMVar_hsa_circ_215684,RMVar_hsa_circ_215683 3963 RMVar_ID_3963 Human_SNP_ID_122380702 A-to-I Human chr3 + 9756284 9756284 9756284 GGATTGCACCAGTGCACTCCAGCCTAGGCAACAGAGCGAGACTCCATCTCAAAAACAAACAAAAA GGATTGCACCAGTGCACTCCAGCCTAGGCAACCGAGCGAGACTCCATCTCAAAAACAAACAAAAA A C OGG1 Ensembl:ENSG00000114026 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1435995678 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84285,RMVar_hsa_circ_292327,RMVar_hsa_circ_215688,RMVar_hsa_circ_215689,RMVar_hsa_circ_363095,RMVar_hsa_circ_379004 3964 RMVar_ID_3964 Human_SNP_ID_122381502 A-to-I Human chr3 + 9758699 9758699 9758699 TTGCCCAGGCTGGAGTGCAGTGGCGCGATCTCAGCTCACTGCAACCCCCATCTCCGAGGTTCAAG TTGCCCAGGCTGGAGTGCAGTGGCGCGATCTCGGCTCACTGCAACCCCCATCTCCGAGGTTCAAG A G OGG1 Ensembl:ENSG00000114026 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1239724166 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_292327,RMVar_hsa_circ_215688 3965 RMVar_ID_3965 Human_SNP_ID_122392091 A-to-I Human chr3 + 9795059 9795059 9795059 ACACAGTCTCGCTCTGTCACCCAGGCTGGAGCACAGTGGCGTGATCTCGGCTCACTGCAACCTCA ACACAGTCTCGCTCTGTCACCCAGGCTGGAGCGCAGTGGCGTGATCTCGGCTCACTGCAACCTCA A G ARPC4-TTLL3,ARPC4 Ensembl:ENSG00000250151,Ensembl:ENSG00000241553 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1205367279 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93902,RMVar_hsa_circ_91750,RMVar_hsa_circ_114779,RMVar_hsa_circ_215706,RMVar_hsa_circ_215707,RMVar_hsa_circ_215708 3966 RMVar_ID_3966 Human_SNP_ID_122392104 A-to-I Human chr3 + 9795091 9795091 9795091 ACAGTGGCGTGATCTCGGCTCACTGCAACCTCAGTCTCCTGGGTTCAAGCAATTCTACTGCCTCA ACAGTGGCGTGATCTCGGCTCACTGCAACCTCTGTCTCCTGGGTTCAAGCAATTCTACTGCCTCA A T ARPC4-TTLL3,ARPC4 Ensembl:ENSG00000250151,Ensembl:ENSG00000241553 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1367083378 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93902,RMVar_hsa_circ_91750,RMVar_hsa_circ_114779,RMVar_hsa_circ_215706,RMVar_hsa_circ_215707,RMVar_hsa_circ_215708 3967 RMVar_ID_3967 Human_SNP_ID_122392129 A-to-I Human chr3 + 9795200 9795200 9795200 TTTTGTATTTTTAGTAGAGACGGGGTTTTGCCATGTTGGCCAGGCTGGTCTTGAACTCCTGACCT TTTTGTATTTTTAGTAGAGACGGGGTTTTGCCGTGTTGGCCAGGCTGGTCTTGAACTCCTGACCT A G ARPC4-TTLL3,ARPC4 Ensembl:ENSG00000250151,Ensembl:ENSG00000241553 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1303812015 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93902,RMVar_hsa_circ_91750,RMVar_hsa_circ_114779,RMVar_hsa_circ_215706,RMVar_hsa_circ_215707,RMVar_hsa_circ_215708 3968 RMVar_ID_3968 Human_SNP_ID_122393533 A-to-I Human chr3 + 9799498 9799498 9799498 GGAGTTTGATTCTGTCACCCAGGCTGGAGTACAGTGGTATGATCTTGGCTCACTGCAACTGCCAC GGAGTTTGATTCTGTCACCCAGGCTGGAGTACGGTGGTATGATCTTGGCTCACTGCAACTGCCAC A G ARPC4-TTLL3,ARPC4 Ensembl:ENSG00000250151,Ensembl:ENSG00000241553 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs999028400 Functional Loss SNV dbSNP153 33..33 33 - - - 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_83967,RMVar_hsa_circ_10453,RMVar_hsa_circ_215710,RMVar_hsa_circ_215711,RMVar_hsa_circ_215709 3969 RMVar_ID_3969 Human_SNP_ID_122394584 A-to-I Human chr3 + 9802791 9802791 9802791 CCACCTCCCAGGTCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTATAGGCACGCA CCACCTCCCAGGTCAAGTGATTCTCCTGCCTCTGCCTCCCGAGTAGCTGGGATTATAGGCACGCA A T ARPC4-TTLL3,ARPC4 Ensembl:ENSG00000250151,Ensembl:ENSG00000241553 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs977651122 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6194,RMVar_hsa_circ_93902,RMVar_hsa_circ_91750,RMVar_hsa_circ_114779,RMVar_hsa_circ_215706,RMVar_hsa_circ_215707,RMVar_hsa_circ_215708,RMVar_hsa_circ_299260,RMVar_hsa_circ_10453,RMVar_hsa_circ_215709,RMVar_hsa_circ_97959,RMVar_hsa_circ_283718,RMVar_hsa_circ_215712,RMVar_hsa_circ_215713,RMVar_hsa_circ_121222,RMVar_hsa_circ_215714 3970 RMVar_ID_3970 Human_SNP_ID_122394647 A-to-I Human chr3 + 9803023 9803023 9803023 CTTCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGTGCCCGCCACCATTCCCGGCTAATTTTT CTTCTGCCTCAGCCTCCCGAGTAGCTGGGACTGCAGGTGCCCGCCACCATTCCCGGCTAATTTTT A G ARPC4-TTLL3,ARPC4 Ensembl:ENSG00000250151,Ensembl:ENSG00000241553 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs567533906 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6194,RMVar_hsa_circ_93902,RMVar_hsa_circ_91750,RMVar_hsa_circ_114779,RMVar_hsa_circ_215706,RMVar_hsa_circ_215707,RMVar_hsa_circ_215708,RMVar_hsa_circ_299260,RMVar_hsa_circ_10453,RMVar_hsa_circ_215709,RMVar_hsa_circ_97959,RMVar_hsa_circ_283718,RMVar_hsa_circ_215712,RMVar_hsa_circ_215713,RMVar_hsa_circ_121222,RMVar_hsa_circ_215714 3971 RMVar_ID_3971 Human_SNP_ID_122397770 A-to-I Human chr3 + 9813578 9813578 9813578 AAGGTGGGAGGATAACTTGAGGCTAGGAGTTCAAGACCAGCCTGGGCAACATAGTAAGACTCAGT AAGGTGGGAGGATAACTTGAGGCTAGGAGTTCGAGACCAGCCTGGGCAACATAGTAAGACTCAGT A G ARPC4-TTLL3,TTLL3 Ensembl:ENSG00000250151,Ensembl:ENSG00000214021 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1414656358 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6194,RMVar_hsa_circ_301884,RMVar_hsa_circ_344559,RMVar_hsa_circ_37234,RMVar_hsa_circ_215717,RMVar_hsa_circ_297996,RMVar_hsa_circ_215722,RMVar_hsa_circ_215723 3972 RMVar_ID_3972 Human_SNP_ID_122398010 A-to-I Human chr3 + 9814484 9814484 9814484 CCGGGCCAACATGGTGAAACCCTGTCTCTACTAAAAAAATAGAAAAATTAGCTGGGTGTAGTGGT CCGGGCCAACATGGTGAAACCCTGTCTCTACTGAAAAAATAGAAAAATTAGCTGGGTGTAGTGGT A G ARPC4-TTLL3,TTLL3 Ensembl:ENSG00000250151,Ensembl:ENSG00000214021 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs976636194 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6194,RMVar_hsa_circ_301884,RMVar_hsa_circ_344559,RMVar_hsa_circ_37234,RMVar_hsa_circ_215717,RMVar_hsa_circ_297996,RMVar_hsa_circ_215722,RMVar_hsa_circ_215723 3973 RMVar_ID_3973 Human_SNP_ID_122398018 A-to-I Human chr3 + 9814511 9814511 9814511 CTACTAAAAAAATAGAAAAATTAGCTGGGTGTAGTGGTGTATGCCTGTAATCACAGCTACTTGGG CTACTAAAAAAATAGAAAAATTAGCTGGGTGTGGTGGTGTATGCCTGTAATCACAGCTACTTGGG A G ARPC4-TTLL3,TTLL3 Ensembl:ENSG00000250151,Ensembl:ENSG00000214021 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1238126146 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6194,RMVar_hsa_circ_301884,RMVar_hsa_circ_344559,RMVar_hsa_circ_37234,RMVar_hsa_circ_215717,RMVar_hsa_circ_297996,RMVar_hsa_circ_215722,RMVar_hsa_circ_215723 3974 RMVar_ID_3974 Human_SNP_ID_122398656 A-to-I Human chr3 + 9816690 9816690 9816690 GGTGCGTGTCACCACACCTGGCTGATTTTTGTATTTTTTAGTAGAGATGGGGTTTCACCATGTTG GGTGCGTGTCACCACACCTGGCTGATTTTTGTGTTTTTTAGTAGAGATGGGGTTTCACCATGTTG A G ARPC4-TTLL3,TTLL3 Ensembl:ENSG00000250151,Ensembl:ENSG00000214021 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1026687352 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6194,RMVar_hsa_circ_301884,RMVar_hsa_circ_344559,RMVar_hsa_circ_215724,RMVar_hsa_circ_293251 3975 RMVar_ID_3975 Human_SNP_ID_122398657 A-to-I Human chr3 + 9816700 9816700 9816700 ACCACACCTGGCTGATTTTTGTATTTTTTAGTAGAGATGGGGTTTCACCATGTTGGTGACCTCAG ACCACACCTGGCTGATTTTTGTATTTTTTAGTGGAGATGGGGTTTCACCATGTTGGTGACCTCAG A G ARPC4-TTLL3,TTLL3 Ensembl:ENSG00000250151,Ensembl:ENSG00000214021 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1451455460 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6194,RMVar_hsa_circ_301884,RMVar_hsa_circ_344559,RMVar_hsa_circ_215724,RMVar_hsa_circ_293251 3976 RMVar_ID_3976 Human_SNP_ID_122398721 A-to-I Human chr3 + 9817006 9817006 9817006 CTTTTTTTATTTTTAAGAGATGAGGTCTTGCTATGCTGCCTAGGCTGGTCTTGAACTCCTGGCCT CTTTTTTTATTTTTAAGAGATGAGGTCTTGCTGTGCTGCCTAGGCTGGTCTTGAACTCCTGGCCT A G ARPC4-TTLL3,TTLL3 Ensembl:ENSG00000250151,Ensembl:ENSG00000214021 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1173570806 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14970415,Human_RBP_ID_17573365,Human_RBP_ID_22286385 RMVar_hsa_circ_6194,RMVar_hsa_circ_301884,RMVar_hsa_circ_344559,RMVar_hsa_circ_215724,RMVar_hsa_circ_293251 3977 RMVar_ID_3977 Human_SNP_ID_122398741 A-to-I Human chr3 + 9817087 9817087 9817087 CTCCCACTTCAGCCTCCCAGAGTGCTGGGATTATAGGTGTGAGCCACCGCGCTCGGCCTTGGCAG CTCCCACTTCAGCCTCCCAGAGTGCTGGGATTGTAGGTGTGAGCCACCGCGCTCGGCCTTGGCAG A G ARPC4-TTLL3,TTLL3 Ensembl:ENSG00000250151,Ensembl:ENSG00000214021 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1423295179 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4755893 RMVar_hsa_circ_6194,RMVar_hsa_circ_301884,RMVar_hsa_circ_344559,RMVar_hsa_circ_215724,RMVar_hsa_circ_293251 3978 RMVar_ID_3978 Human_SNP_ID_122398762 A-to-I Human chr3 + 9817169 9817158 9817170 AGGGTGGGCCGGGCACAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGCAG AGGGTGGGCCGGGCACAGTGGC____________TCCCAGCACTTTGGGAGGCCGAGGCAGGCAG CTCACGCCTGTAA C ARPC4-TTLL3,TTLL3 Ensembl:ENSG00000250151,Ensembl:ENSG00000214021 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs755629870 Functional Loss DEL dbSNP153 23..34 33 - - - RMVar_hsa_circ_6194,RMVar_hsa_circ_301884,RMVar_hsa_circ_344559,RMVar_hsa_circ_215724,RMVar_hsa_circ_293251 3979 RMVar_ID_3979 Human_SNP_ID_122398797 A-to-I Human chr3 + 9817261 9817261 9817261 CCTGGCTAACACGGTGAAATGCCGTCTCTATTAAAAATACAACAAATTAGCTGGATGTGGTGTCG CCTGGCTAACACGGTGAAATGCCGTCTCTATTTAAAATACAACAAATTAGCTGGATGTGGTGTCG A T ARPC4-TTLL3,TTLL3 Ensembl:ENSG00000250151,Ensembl:ENSG00000214021 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1019730925 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6194,RMVar_hsa_circ_301884,RMVar_hsa_circ_344559,RMVar_hsa_circ_215724,RMVar_hsa_circ_293251 3980 RMVar_ID_3980 Human_SNP_ID_122398798 A-to-I Human chr3 + 9817272 9817272 9817272 CGGTGAAATGCCGTCTCTATTAAAAATACAACAAATTAGCTGGATGTGGTGTCGGGCGCCTGTAG CGGTGAAATGCCGTCTCTATTAAAAATACAACGAATTAGCTGGATGTGGTGTCGGGCGCCTGTAG A G ARPC4-TTLL3,TTLL3 Ensembl:ENSG00000250151,Ensembl:ENSG00000214021 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1296869498 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6194,RMVar_hsa_circ_301884,RMVar_hsa_circ_344559,RMVar_hsa_circ_215724,RMVar_hsa_circ_293251 3981 RMVar_ID_3981 Human_SNP_ID_122398810 A-to-I Human chr3 + 9817313 9817313 9817313 GGATGTGGTGTCGGGCGCCTGTAGTCCCAGCTACTCTGGAGGCCGAGGCAGGAGAATGGTGTGAA GGATGTGGTGTCGGGCGCCTGTAGTCCCAGCTCCTCTGGAGGCCGAGGCAGGAGAATGGTGTGAA A C ARPC4-TTLL3,TTLL3 Ensembl:ENSG00000250151,Ensembl:ENSG00000214021 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs573062970 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_156547 RMVar_hsa_circ_6194,RMVar_hsa_circ_301884,RMVar_hsa_circ_344559,RMVar_hsa_circ_215724,RMVar_hsa_circ_293251 3982 RMVar_ID_3982 Human_SNP_ID_122401729 A-to-I Human chr3 + 9827520 9827520 9827520 GACTTCCTGTGCTCAAGCAATCCTTCCTCCTCAGCCTCCCAAGTGTCTGAGACCACAGGCATGTA GACTTCCTGTGCTCAAGCAATCCTTCCTCCTCCGCCTCCCAAGTGTCTGAGACCACAGGCATGTA A C ARPC4-TTLL3,TTLL3 Ensembl:ENSG00000250151,Ensembl:ENSG00000214021 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs942571494 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_344559,RMVar_hsa_circ_36155,RMVar_hsa_circ_346108,RMVar_hsa_circ_215725,RMVar_hsa_circ_314566,RMVar_hsa_circ_215727 3983 RMVar_ID_3983 Human_SNP_ID_122404290 A-to-I Human chr3 + 9836178 9836178 9836178 AAAATTAGCTGGGTGTGGTGGCACACACCTGTAGTCCTAGCTACTCGGGAGGCCTAGGTGGGAGG AAAATTAGCTGGGTGTGGTGGCACACACCTGTGGTCCTAGCTACTCGGGAGGCCTAGGTGGGAGG A G TTLL3 Ensembl:ENSG00000214021 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1134280 Functional Loss SNV dbSNP153 33..33 33 - - - 3984 RMVar_ID_3984 Human_SNP_ID_122422161 A-to-I Human chr3 + 9895909 9895909 9895909 CTTAATAGAGACAGGGTCTCACTATGTTGGCCAGACTGGTCTTGAACTCCTGACCTCAGATGATC CTTAATAGAGACAGGGTCTCACTATGTTGGCCGGACTGGTCTTGAACTCCTGACCTCAGATGATC A G lnc-BBS5-6 RNACentral:URS0000E2127A lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1411497464 Functional Loss SNV dbSNP153 33..33 33 - - - 3985 RMVar_ID_3985 Human_SNP_ID_122428812 A-to-I Human chr3 + 9918770 9918770 9918770 GTGTTTTACAGGTATCAACTTATTTAATTCTCACAACAGCCATGTGAGGTGGGACTATTCTTTTG GTGTTTTACAGGTATCAACTTATTTAATTCTCGCAACAGCCATGTGAGGTGGGACTATTCTTTTG A G IL17RC Ensembl:ENSG00000163702 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042909474 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17573999 RMVar_hsa_circ_29996 3986 RMVar_ID_3986 Human_SNP_ID_122429036 A-to-I Human chr3 + 9919659 9919659 9919659 CAGAGCGAGATTCCGTCTCAAAAAAAAAGAATAGTCCCACCTCACATGACTGTTGTGAGAATTAA CAGAGCGAGATTCCGTCTCAAAAAAAAAGAATGGTCCCACCTCACATGACTGTTGTGAGAATTAA A G IL17RC Ensembl:ENSG00000163702 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1191017516 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29996 3987 RMVar_ID_3987 Human_SNP_ID_122436875 A-to-I Human chr3 + 9943587 9943587 9943587 GAGAAGGCAGGCAAGCCCCTTCCCCAGGTAGCAGTGGCAGCTCCAGGCCCTGCCCCATCCCTACT GAGAAGGCAGGCAAGCCCCTTCCCCAGGTAGCCGTGGCAGCTCCAGGCCCTGCCCCATCCCTACT A C AC018809.3,CRELD1 Ensembl:ENSG00000288550,Ensembl:ENSG00000163703 Protein coding,Protein coding intron,intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs568291553 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_932825,Human_RBP_ID_5390502,Human_RBP_ID_17088798,Human_RBP_ID_22363048,Human_RBP_ID_22607516,Human_RBP_ID_22675972,Human_RBP_ID_22725700 3988 RMVar_ID_3988 Human_SNP_ID_122441296 A-to-I Human chr3 - 9957966 9957966 9957966 TTACCAGAATTTTTTTTTTTTTTTGAGACAGAATCTTGCTCTGTCACCCAGGCTGGCGTGCAGTG TTACCAGAATTTTTTTTTTTTTTTGAGACAGACTCTTGCTCTGTCACCCAGGCTGGCGTGCAGTG T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1286460162 Functional Loss SNV dbSNP153 33..33 33 - - - 3989 RMVar_ID_3989 Human_SNP_ID_122447815 A-to-I Human chr3 - 9982792 9982791 9982792 AGCCTCAACATCTCAGGCTCAAGGATCCTCCCACCTCAGCCTCTCGAGTAGCTGGGATTATAAGC AGCCTCAACATCTCAGGCTCAAGGATCCTCCC_CCTCAGCCTCTCGAGTAGCTGGGATTATAAGC GT G EMC3 Ensembl:ENSG00000125037 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167329141 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_108738,RMVar_hsa_circ_215742,RMVar_hsa_circ_340033,RMVar_hsa_circ_320587 3990 RMVar_ID_3990 Human_SNP_ID_122449869 A-to-I Human chr3 + 9990044 9990044 9990044 ACTCCCAGTGTTTTCTCTTTTTTTTTTGAGACAGAGTCTTGCTCTGTCACCCAGGCTGGAGTGCA ACTCCCAGTGTTTTCTCTTTTTTTTTTGAGACGGAGTCTTGCTCTGTCACCCAGGCTGGAGTGCA A G EMC3-AS1 Ensembl:ENSG00000180385 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886806068 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14544451 RMVar_hsa_circ_107386,RMVar_hsa_circ_215751 3991 RMVar_ID_3991 Human_SNP_ID_122451446 A-to-I Human chr3 + 9995763 9995763 9995763 GGGTTCTAGCGATTCTCCTGCCTCACCCTTCCAAGTACCTGGGACTACAGGCACGTGTCACCACA GGGTTCTAGCGATTCTCCTGCCTCACCCTTCCGAGTACCTGGGACTACAGGCACGTGTCACCACA A G EMC3-AS1 Ensembl:ENSG00000180385 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005791693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18342030 RMVar_hsa_circ_107386,RMVar_hsa_circ_215751 3992 RMVar_ID_3992 Human_SNP_ID_122451611 A-to-I Human chr3 + 9996384 9996384 9996384 GGAGGATCCATTGAACCCAGGGAGTTGAGGCTACAGTGAGCCATGATTGTGCCACTGCTCTCCAG GGAGGATCCATTGAACCCAGGGAGTTGAGGCTCCAGTGAGCCATGATTGTGCCACTGCTCTCCAG A C EMC3-AS1 Ensembl:ENSG00000180385 Pseudogene intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs779847852 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107386,RMVar_hsa_circ_215751 3993 RMVar_ID_3993 Human_SNP_ID_122451857 A-to-I Human chr3 + 9997313 9997313 9997313 AGGATGGTCTCGATCTCCTGACCTCGTGATCTACCCGCCTCGCCCTCCCAAAGTCCTGGGATTAC AGGATGGTCTCGATCTCCTGACCTCGTGATCTCCCCGCCTCGCCCTCCCAAAGTCCTGGGATTAC A C EMC3-AS1 Ensembl:ENSG00000180385 Pseudogene intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1045552787 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14544805 RMVar_hsa_circ_107386,RMVar_hsa_circ_215751 3994 RMVar_ID_3994 Human_SNP_ID_122452258 A-to-I Human chr3 + 9998499 9998499 9998499 TCACCCAGGCTGCAGTGCAGTGGCGTGATCATAGTTCACTGCAGCCTGAAACTCCTGGGCTCAAG TCACCCAGGCTGCAGTGCAGTGGCGTGATCATGGTTCACTGCAGCCTGAAACTCCTGGGCTCAAG A G EMC3-AS1 Ensembl:ENSG00000180385 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs538934156 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5250107,Human_RBP_ID_8553892,Human_RBP_ID_17573506 RMVar_hsa_circ_107386,RMVar_hsa_circ_215751 3995 RMVar_ID_3995 Human_SNP_ID_122452259 A-to-I Human chr3 + 9998499 9998499 9998499 TCACCCAGGCTGCAGTGCAGTGGCGTGATCATAGTTCACTGCAGCCTGAAACTCCTGGGCTCAAG TCACCCAGGCTGCAGTGCAGTGGCGTGATCATTGTTCACTGCAGCCTGAAACTCCTGGGCTCAAG A T EMC3-AS1 Ensembl:ENSG00000180385 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs538934156 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5250107,Human_RBP_ID_8553892,Human_RBP_ID_17573506 RMVar_hsa_circ_107386,RMVar_hsa_circ_215751 3996 RMVar_ID_3996 Human_SNP_ID_122452336 A-to-I Human chr3 + 9998831 9998831 9998831 CAAGTTGGAGTGCAGTGGTATGATCCTGGCTCACTGCAACCTCCACTTCCGAGGCTCAAGCGATC CAAGTTGGAGTGCAGTGGTATGATCCTGGCTCGCTGCAACCTCCACTTCCGAGGCTCAAGCGATC A G EMC3-AS1 Ensembl:ENSG00000180385 Pseudogene intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs541095850 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7097172,Human_RBP_ID_14544880,Human_RBP_ID_18341923 RMVar_hsa_circ_107386,RMVar_hsa_circ_215751 3997 RMVar_ID_3997 Human_SNP_ID_122452364 A-to-I Human chr3 + 9998941 9998941 9998941 ATGGTGCCCCGCTAATTTTTTGCAATTTTGGTAGACATAAGGTTTCGTCATGTTACCCAGACTGG ATGGTGCCCCGCTAATTTTTTGCAATTTTGGTGGACATAAGGTTTCGTCATGTTACCCAGACTGG A G EMC3-AS1 Ensembl:ENSG00000180385 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1241979630 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5250108,Human_RBP_ID_8264734,Human_RBP_ID_14544895,Human_RBP_ID_18536144,Human_RBP_ID_20971698 RMVar_hsa_circ_107386,RMVar_hsa_circ_215751 3998 RMVar_ID_3998 Human_SNP_ID_122452370 A-to-I Human chr3 + 9998963 9998963 9998963 CAATTTTGGTAGACATAAGGTTTCGTCATGTTACCCAGACTGGTCTCGAACTTTTGAGCTTAGGA CAATTTTGGTAGACATAAGGTTTCGTCATGTTGCCCAGACTGGTCTCGAACTTTTGAGCTTAGGA A G EMC3-AS1 Ensembl:ENSG00000180385 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1435603125 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1383185,Human_RBP_ID_7097176,Human_RBP_ID_8264734,Human_RBP_ID_14544895,Human_RBP_ID_18517213,Human_RBP_ID_18536582,Human_RBP_ID_23188076 RMVar_hsa_circ_107386,RMVar_hsa_circ_215751 3999 RMVar_ID_3999 Human_SNP_ID_122452473 A-to-I Human chr3 + 9999345 9999345 9999345 CTCTCTGCAATCTCTACCTTGCGGGTTCAGACAATTCTCCTGCCTCAGCCTCCCGTGTAGCTGGG CTCTCTGCAATCTCTACCTTGCGGGTTCAGACGATTCTCCTGCCTCAGCCTCCCGTGTAGCTGGG A G EMC3-AS1 Ensembl:ENSG00000180385 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1247215421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5250109,Human_RBP_ID_14544917 Human_miRNA_ID_2238221,Human_miRNA_ID_2712830,Human_miRNA_ID_3048810 RMVar_hsa_circ_107386,RMVar_hsa_circ_215751 4000 RMVar_ID_4000 Human_SNP_ID_122452605 A-to-I Human chr3 + 9999953 9999953 9999953 TGGTTCTAAGACAGTGAGGAAATTTCCCCAGTATTTAAATATATTCACATAACCAGTTAAATAAA TGGTTCTAAGACAGTGAGGAAATTTCCCCAGTTTTTAAATATATTCACATAACCAGTTAAATAAA A T EMC3-AS1 Ensembl:ENSG00000180385 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1291533655 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107386,RMVar_hsa_circ_215751 4001 RMVar_ID_4001 Human_SNP_ID_122453105 A-to-I Human chr3 + 10001754 10001754 10001754 GTGCTGTGGCTAACGCCTGTAATTCCAGCACTATGAGAGACCGAGGCGGGCAGATCACGAGTTCA GTGCTGTGGCTAACGCCTGTAATTCCAGCACTGTGAGAGACCGAGGCGGGCAGATCACGAGTTCA A G EMC3-AS1 Ensembl:ENSG00000180385 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1231306414 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7097287,Human_RBP_ID_14545302,Human_RBP_ID_17405281,Human_RBP_ID_18517216,Human_RBP_ID_25684383 RMVar_hsa_circ_107386,RMVar_hsa_circ_215751 4002 RMVar_ID_4002 Human_SNP_ID_122453157 A-to-I Human chr3 + 10001924 10001924 10001924 AGGAGGCTGAGGCAGGAGAATTGCATGAACCCAGGAGGTGGAGCTTGCAGTGAGCCGAGATCACG AGGAGGCTGAGGCAGGAGAATTGCATGAACCCTGGAGGTGGAGCTTGCAGTGAGCCGAGATCACG A T EMC3-AS1 Ensembl:ENSG00000180385 Pseudogene intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs534402460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17405282 RMVar_hsa_circ_107386,RMVar_hsa_circ_215751 4003 RMVar_ID_4003 Human_SNP_ID_122453342 A-to-I Human chr3 + 10002486 10002486 10002486 TTCTGTATTTTCTATAGAGATGAGGTTTTGCCATGTTACCCAGGCTGGTCTTGAACTCCTGGGAT TTCTGTATTTTCTATAGAGATGAGGTTTTGCCGTGTTACCCAGGCTGGTCTTGAACTCCTGGGAT A G EMC3-AS1 Ensembl:ENSG00000180385 Pseudogene intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1264659282 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107386,RMVar_hsa_circ_215751 4004 RMVar_ID_4004 Human_SNP_ID_122457759 A-to-I Human chr3 - 10018179 10018179 10018179 GTTGGCCACACTGGTCTCAAACTCCTGACCTCAGGTGACTCACCCACCACGGCCTCCCAAAGTGT GTTGGCCACACTGGTCTCAAACTCCTGACCTCGGGTGACTCACCCACCACGGCCTCCCAAAGTGT T C CIDECP1 Ensembl:ENSG00000186162 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1222370348 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17405333 RMVar_hsa_circ_215750 4005 RMVar_ID_4005 Human_SNP_ID_122458060 A-to-I Human chr3 - 10019538 10019538 10019538 GTTCTTTAATACTTTTGTAGAGACAAGGTCTCACTAGACCAGGCTGGTCTCAAACTCCTGGCCTC GTTCTTTAATACTTTTGTAGAGACAAGGTCTCTCTAGACCAGGCTGGTCTCAAACTCCTGGCCTC T A CIDECP1 Ensembl:ENSG00000186162 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928165544 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5250062 RMVar_hsa_circ_215750 4006 RMVar_ID_4006 Human_SNP_ID_122458061 A-to-I Human chr3 - 10019538 10019538 10019538 GTTCTTTAATACTTTTGTAGAGACAAGGTCTCACTAGACCAGGCTGGTCTCAAACTCCTGGCCTC GTTCTTTAATACTTTTGTAGAGACAAGGTCTCGCTAGACCAGGCTGGTCTCAAACTCCTGGCCTC T C CIDECP1 Ensembl:ENSG00000186162 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928165544 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5250062 RMVar_hsa_circ_215750 4007 RMVar_ID_4007 Human_SNP_ID_122458074 A-to-I Human chr3 - 10019623 10019623 10019623 GCAATCATGGCTCACTGCAGCCTTAACCTCGTAGGCTCAAGTGATCCTCCTGAGTAGCACAAGTG GCAATCATGGCTCACTGCAGCCTTAACCTCGTGGGCTCAAGTGATCCTCCTGAGTAGCACAAGTG T C CIDECP1 Ensembl:ENSG00000186162 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1361921563 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_215750 4008 RMVar_ID_4008 Human_SNP_ID_122458313 A-to-I Human chr3 - 10020586 10020586 10020586 GCTGGAGTGCAGTGGCGCGATCTCAGCTCACTACAACCTCTGCCTTCCAGGTTCAAGCAGCCTCA GCTGGAGTGCAGTGGCGCGATCTCAGCTCACTGCAACCTCTGCCTTCCAGGTTCAAGCAGCCTCA T C CIDECP1 Ensembl:ENSG00000186162 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1220604347 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_215750 4009 RMVar_ID_4009 Human_SNP_ID_122458898 A-to-I Human chr3 - 10022803 10022803 10022803 CAGTAAGAATGATGAGATAGGCTGGGTGCAGTAGCTCTCACCTGGAATCCCAGCACTTTGGGAGT CAGTAAGAATGATGAGATAGGCTGGGTGCAGTGGCTCTCACCTGGAATCCCAGCACTTTGGGAGT T C CIDECP1 Ensembl:ENSG00000186162 Pseudogene intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1436126166 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5250064,Human_RBP_ID_10113490,Human_RBP_ID_14548358,Human_RBP_ID_23956020 RMVar_hsa_circ_215750 4010 RMVar_ID_4010 Human_SNP_ID_122458981 A-to-I Human chr3 - 10023051 10023051 10023051 ATGCCTGTAATCCCAACTACTCAGGAGCCTGAAGCAGGAGAATCGTTTGAACCCAGGAGGTGGAG ATGCCTGTAATCCCAACTACTCAGGAGCCTGACGCAGGAGAATCGTTTGAACCCAGGAGGTGGAG T G CIDECP1 Ensembl:ENSG00000186162 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1020417623 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_215750 4011 RMVar_ID_4011 Human_SNP_ID_122460559 A-to-I Human chr3 + 10029354 10029354 10029354 AGACTCCATCTCTACAAAAAATTTTTTTAATTAGCTGGGCATGGTGGTTTGTGCCTGTGGTCCCA AGACTCCATCTCTACAAAAAATTTTTTTAATTTGCTGGGCATGGTGGTTTGTGCCTGTGGTCCCA A T FANCD2 Ensembl:ENSG00000144554 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1203546927 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17990122 RMVar_hsa_circ_105839,RMVar_hsa_circ_123116,RMVar_hsa_circ_94005,RMVar_hsa_circ_215753,RMVar_hsa_circ_115336,RMVar_hsa_circ_215754,RMVar_hsa_circ_215755,RMVar_hsa_circ_215756 4012 RMVar_ID_4012 Human_SNP_ID_122460568 A-to-I Human chr3 + 10029416 10029416 10029416 CCAGCTACTGAGGAGGCTGAAGTGGAAGGATCACTTGAGCTCAGGAGGTCGAGGGTGCAATGAGT CCAGCTACTGAGGAGGCTGAAGTGGAAGGATCGCTTGAGCTCAGGAGGTCGAGGGTGCAATGAGT A G FANCD2 Ensembl:ENSG00000144554 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs971614490 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105839,RMVar_hsa_circ_123116,RMVar_hsa_circ_94005,RMVar_hsa_circ_215753,RMVar_hsa_circ_115336,RMVar_hsa_circ_215754,RMVar_hsa_circ_215755,RMVar_hsa_circ_215756 4013 RMVar_ID_4013 Human_SNP_ID_122460569 A-to-I Human chr3 + 10029416 10029416 10029416 CCAGCTACTGAGGAGGCTGAAGTGGAAGGATCACTTGAGCTCAGGAGGTCGAGGGTGCAATGAGT CCAGCTACTGAGGAGGCTGAAGTGGAAGGATCTCTTGAGCTCAGGAGGTCGAGGGTGCAATGAGT A T FANCD2 Ensembl:ENSG00000144554 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs971614490 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105839,RMVar_hsa_circ_123116,RMVar_hsa_circ_94005,RMVar_hsa_circ_215753,RMVar_hsa_circ_115336,RMVar_hsa_circ_215754,RMVar_hsa_circ_215755,RMVar_hsa_circ_215756 4014 RMVar_ID_4014 Human_SNP_ID_122460702 A-to-I Human chr3 + 10029960 10029960 10029960 CGCCAGCCACCATGCCCGGCTGATTTTTTTGTATCTTTAGTAGAGACGGGGTTTCACCATGCTGG CGCCAGCCACCATGCCCGGCTGATTTTTTTGTGTCTTTAGTAGAGACGGGGTTTCACCATGCTGG A G FANCD2 Ensembl:ENSG00000144554 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs183013082 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14548446 RMVar_hsa_circ_105839,RMVar_hsa_circ_123116,RMVar_hsa_circ_94005,RMVar_hsa_circ_215753,RMVar_hsa_circ_115336,RMVar_hsa_circ_215754,RMVar_hsa_circ_215755,RMVar_hsa_circ_215756 4015 RMVar_ID_4015 Human_SNP_ID_122460703 A-to-I Human chr3 + 10029960 10029960 10029960 CGCCAGCCACCATGCCCGGCTGATTTTTTTGTATCTTTAGTAGAGACGGGGTTTCACCATGCTGG CGCCAGCCACCATGCCCGGCTGATTTTTTTGTTTCTTTAGTAGAGACGGGGTTTCACCATGCTGG A T FANCD2 Ensembl:ENSG00000144554 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs183013082 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14548446 RMVar_hsa_circ_105839,RMVar_hsa_circ_123116,RMVar_hsa_circ_94005,RMVar_hsa_circ_215753,RMVar_hsa_circ_115336,RMVar_hsa_circ_215754,RMVar_hsa_circ_215755,RMVar_hsa_circ_215756 4016 RMVar_ID_4016 Human_SNP_ID_122460818 A-to-I Human chr3 + 10030302 10030302 10030302 TATTTTTAGTAGAGAAGGGGTTTCACCGTGTTAGTCAGGCTGGTCTCAAACTCCTGACCTCCGGT TATTTTTAGTAGAGAAGGGGTTTCACCGTGTTGGTCAGGCTGGTCTCAAACTCCTGACCTCCGGT A G FANCD2 Ensembl:ENSG00000144554 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1348954249 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105839,RMVar_hsa_circ_123116,RMVar_hsa_circ_94005,RMVar_hsa_circ_215753,RMVar_hsa_circ_115336,RMVar_hsa_circ_215754,RMVar_hsa_circ_215755,RMVar_hsa_circ_215756 4017 RMVar_ID_4017 Human_SNP_ID_122462019 A-to-I Human chr3 + 10034203 10034203 10034203 AAACGAAACAAAACAAAAAAAAACGTGTCTGTAGTCCCAGCTACTTGGGGGGGCTGAGGCAGGAG AAACGAAACAAAACAAAAAAAAACGTGTCTGTCGTCCCAGCTACTTGGGGGGGCTGAGGCAGGAG A C FANCD2 Ensembl:ENSG00000144554 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs940466693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14548495 RMVar_hsa_circ_4119,RMVar_hsa_circ_105839,RMVar_hsa_circ_123116,RMVar_hsa_circ_94005,RMVar_hsa_circ_215753,RMVar_hsa_circ_115336,RMVar_hsa_circ_215754,RMVar_hsa_circ_215755,RMVar_hsa_circ_215756,RMVar_hsa_circ_114606,RMVar_hsa_circ_215757,RMVar_hsa_circ_394 4018 RMVar_ID_4018 Human_SNP_ID_122462020 A-to-I Human chr3 + 10034203 10034203 10034203 AAACGAAACAAAACAAAAAAAAACGTGTCTGTAGTCCCAGCTACTTGGGGGGGCTGAGGCAGGAG AAACGAAACAAAACAAAAAAAAACGTGTCTGTGGTCCCAGCTACTTGGGGGGGCTGAGGCAGGAG A G FANCD2 Ensembl:ENSG00000144554 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs940466693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14548495 RMVar_hsa_circ_4119,RMVar_hsa_circ_105839,RMVar_hsa_circ_123116,RMVar_hsa_circ_94005,RMVar_hsa_circ_215753,RMVar_hsa_circ_115336,RMVar_hsa_circ_215754,RMVar_hsa_circ_215755,RMVar_hsa_circ_215756,RMVar_hsa_circ_114606,RMVar_hsa_circ_215757,RMVar_hsa_circ_394 4019 RMVar_ID_4019 Human_SNP_ID_122465588 A-to-I Human chr3 + 10046260 10046260 10046260 TATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGTCAGGATGGTCTCGATCTCCTGACCTTGTGA TATTTTTAGTAGAGACGGGGTTTCACCGTGTTGGTCAGGATGGTCTCGATCTCCTGACCTTGTGA A G FANCD2 Ensembl:ENSG00000144554 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs571664921 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_96251,RMVar_hsa_circ_104365,RMVar_hsa_circ_215757,RMVar_hsa_circ_105130,RMVar_hsa_circ_215759,RMVar_hsa_circ_80013,RMVar_hsa_circ_215760,RMVar_hsa_circ_215758,RMVar_hsa_circ_77614,RMVar_hsa_circ_215763,RMVar_hsa_circ_120008,RMVar_hsa_circ_215761,RMVar_hsa_circ_99141,RMVar_hsa_circ_215764,RMVar_hsa_circ_117723,RMVar_hsa_circ_84203,RMVar_hsa_circ_215765,RMVar_hsa_circ_45778,RMVar_hsa_circ_215766,RMVar_hsa_circ_127017,RMVar_hsa_circ_215768,RMVar_hsa_circ_215767,RMVar_hsa_circ_119841,RMVar_hsa_circ_122156,RMVar_hsa_circ_215771,RMVar_hsa_circ_215772 4020 RMVar_ID_4020 Human_SNP_ID_122469990 A-to-I Human chr3 + 10059685 10059685 10059685 TTATCCGGGCGTGGTTGGTGGCGGGCACCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA TTATCCGGGCGTGGTTGGTGGCGGGCACCTGTGGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA A G FANCD2 Ensembl:ENSG00000144554 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1425362636 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_154789 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 4021 RMVar_ID_4021 Human_SNP_ID_122470950 A-to-I Human chr3 + 10063330 10063330 10063330 ATGGTGGCAGGCGCCTGTAGTCCCAGCTACTCAGGAGGCTGGGGCAAGAGAATTGCTTGAATCCG ATGGTGGCAGGCGCCTGTAGTCCCAGCTACTCTGGAGGCTGGGGCAAGAGAATTGCTTGAATCCG A T FANCD2 Ensembl:ENSG00000144554 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1277349091 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123116,RMVar_hsa_circ_215754,RMVar_hsa_circ_114606,RMVar_hsa_circ_215757,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_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_92781,RMVar_hsa_circ_75780,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,RMVar_hsa_circ_94327,RMVar_hsa_circ_60378,RMVar_hsa_circ_112809,RMVar_hsa_circ_215783,RMVar_hsa_circ_376157,RMVar_hsa_circ_71957,RMVar_hsa_circ_215787,RMVar_hsa_circ_215788 4022 RMVar_ID_4022 Human_SNP_ID_122474912 A-to-I Human chr3 + 10076148 10076148 10076148 CAGTGAGACTGTATTTCACCCATTCTGCTTCTAGCAGTGTAATATAGCTATTCCACTGGGATCAC CAGTGAGACTGTATTTCACCCATTCTGCTTCTGGCAGTGTAATATAGCTATTCCACTGGGATCAC A G FANCD2 Ensembl:ENSG00000144554 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs401900 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123116,RMVar_hsa_circ_215754,RMVar_hsa_circ_80013,RMVar_hsa_circ_215758,RMVar_hsa_circ_120008,RMVar_hsa_circ_215764,RMVar_hsa_circ_117723,RMVar_hsa_circ_215766,RMVar_hsa_circ_127017,RMVar_hsa_circ_215767,RMVar_hsa_circ_119841,RMVar_hsa_circ_20779,RMVar_hsa_circ_124318,RMVar_hsa_circ_215771,RMVar_hsa_circ_92781,RMVar_hsa_circ_215779,RMVar_hsa_circ_55648,RMVar_hsa_circ_215778,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,RMVar_hsa_circ_94327,RMVar_hsa_circ_78921,RMVar_hsa_circ_112809,RMVar_hsa_circ_215783,RMVar_hsa_circ_376157,RMVar_hsa_circ_215787,RMVar_hsa_circ_215788,RMVar_hsa_circ_89275,RMVar_hsa_circ_215789,RMVar_hsa_circ_215790,RMVar_hsa_circ_115110,RMVar_hsa_circ_215791,RMVar_hsa_circ_215796,RMVar_hsa_circ_274249,RMVar_hsa_circ_77802,RMVar_hsa_circ_98181,RMVar_hsa_circ_215793,RMVar_hsa_circ_215794,RMVar_hsa_circ_304597,RMVar_hsa_circ_292652,RMVar_hsa_circ_10723,RMVar_hsa_circ_93917,RMVar_hsa_circ_105425,RMVar_hsa_circ_85383,RMVar_hsa_circ_215800,RMVar_hsa_circ_215798,RMVar_hsa_circ_215799,RMVar_hsa_circ_215797,RMVar_hsa_circ_48326,RMVar_hsa_circ_215795,RMVar_hsa_circ_332648,RMVar_hsa_circ_299480 4023 RMVar_ID_4023 Human_SNP_ID_122474913 A-to-I Human chr3 + 10076148 10076148 10076148 CAGTGAGACTGTATTTCACCCATTCTGCTTCTAGCAGTGTAATATAGCTATTCCACTGGGATCAC CAGTGAGACTGTATTTCACCCATTCTGCTTCTTGCAGTGTAATATAGCTATTCCACTGGGATCAC A T FANCD2 Ensembl:ENSG00000144554 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs401900 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123116,RMVar_hsa_circ_215754,RMVar_hsa_circ_80013,RMVar_hsa_circ_215758,RMVar_hsa_circ_120008,RMVar_hsa_circ_215764,RMVar_hsa_circ_117723,RMVar_hsa_circ_215766,RMVar_hsa_circ_127017,RMVar_hsa_circ_215767,RMVar_hsa_circ_119841,RMVar_hsa_circ_20779,RMVar_hsa_circ_124318,RMVar_hsa_circ_215771,RMVar_hsa_circ_92781,RMVar_hsa_circ_215779,RMVar_hsa_circ_55648,RMVar_hsa_circ_215778,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,RMVar_hsa_circ_94327,RMVar_hsa_circ_78921,RMVar_hsa_circ_112809,RMVar_hsa_circ_215783,RMVar_hsa_circ_376157,RMVar_hsa_circ_215787,RMVar_hsa_circ_215788,RMVar_hsa_circ_89275,RMVar_hsa_circ_215789,RMVar_hsa_circ_215790,RMVar_hsa_circ_115110,RMVar_hsa_circ_215791,RMVar_hsa_circ_215796,RMVar_hsa_circ_274249,RMVar_hsa_circ_77802,RMVar_hsa_circ_98181,RMVar_hsa_circ_215793,RMVar_hsa_circ_215794,RMVar_hsa_circ_304597,RMVar_hsa_circ_292652,RMVar_hsa_circ_10723,RMVar_hsa_circ_93917,RMVar_hsa_circ_105425,RMVar_hsa_circ_85383,RMVar_hsa_circ_215800,RMVar_hsa_circ_215798,RMVar_hsa_circ_215799,RMVar_hsa_circ_215797,RMVar_hsa_circ_48326,RMVar_hsa_circ_215795,RMVar_hsa_circ_332648,RMVar_hsa_circ_299480 4024 RMVar_ID_4024 Human_SNP_ID_122475104 A-to-I Human chr3 + 10076916 10076916 10076916 TGGGATTACAGGTGCCCACCACCACATCAGCTAATTTTTGTATTTTTAGTAGAGATGGGATTTCA TGGGATTACAGGTGCCCACCACCACATCAGCTGATTTTTGTATTTTTAGTAGAGATGGGATTTCA A G FANCD2 Ensembl:ENSG00000144554 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs899307085 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123116,RMVar_hsa_circ_215754,RMVar_hsa_circ_80013,RMVar_hsa_circ_215758,RMVar_hsa_circ_120008,RMVar_hsa_circ_215764,RMVar_hsa_circ_117723,RMVar_hsa_circ_215766,RMVar_hsa_circ_127017,RMVar_hsa_circ_215767,RMVar_hsa_circ_119841,RMVar_hsa_circ_20779,RMVar_hsa_circ_124318,RMVar_hsa_circ_215771,RMVar_hsa_circ_92781,RMVar_hsa_circ_215779,RMVar_hsa_circ_55648,RMVar_hsa_circ_215778,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,RMVar_hsa_circ_94327,RMVar_hsa_circ_78921,RMVar_hsa_circ_112809,RMVar_hsa_circ_215783,RMVar_hsa_circ_376157,RMVar_hsa_circ_215787,RMVar_hsa_circ_215788,RMVar_hsa_circ_89275,RMVar_hsa_circ_215789,RMVar_hsa_circ_215790,RMVar_hsa_circ_115110,RMVar_hsa_circ_215791,RMVar_hsa_circ_215796,RMVar_hsa_circ_274249,RMVar_hsa_circ_77802,RMVar_hsa_circ_98181,RMVar_hsa_circ_215793,RMVar_hsa_circ_215794,RMVar_hsa_circ_304597,RMVar_hsa_circ_292652,RMVar_hsa_circ_10723,RMVar_hsa_circ_93917,RMVar_hsa_circ_105425,RMVar_hsa_circ_85383,RMVar_hsa_circ_215800,RMVar_hsa_circ_215798,RMVar_hsa_circ_215799,RMVar_hsa_circ_215797,RMVar_hsa_circ_48326,RMVar_hsa_circ_215795,RMVar_hsa_circ_332648,RMVar_hsa_circ_299480 4025 RMVar_ID_4025 Human_SNP_ID_122475659 A-to-I Human chr3 + 10078842 10078842 10078842 AAAAAGAACTAGCCGGGCATGGTGGTGCAGCTATAGTTCCAGCTACTTGGGAGGCTGAGGCATGG AAAAAGAACTAGCCGGGCATGGTGGTGCAGCTCTAGTTCCAGCTACTTGGGAGGCTGAGGCATGG A C FANCD2 Ensembl:ENSG00000144554 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs981751213 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123116,RMVar_hsa_circ_215754,RMVar_hsa_circ_80013,RMVar_hsa_circ_215758,RMVar_hsa_circ_120008,RMVar_hsa_circ_215764,RMVar_hsa_circ_117723,RMVar_hsa_circ_215766,RMVar_hsa_circ_127017,RMVar_hsa_circ_215767,RMVar_hsa_circ_119841,RMVar_hsa_circ_124318,RMVar_hsa_circ_215771,RMVar_hsa_circ_92781,RMVar_hsa_circ_215779,RMVar_hsa_circ_55648,RMVar_hsa_circ_215778,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,RMVar_hsa_circ_94327,RMVar_hsa_circ_78921,RMVar_hsa_circ_112809,RMVar_hsa_circ_215783,RMVar_hsa_circ_376157,RMVar_hsa_circ_215787,RMVar_hsa_circ_215788,RMVar_hsa_circ_89275,RMVar_hsa_circ_215789,RMVar_hsa_circ_215790,RMVar_hsa_circ_115110,RMVar_hsa_circ_215791,RMVar_hsa_circ_215796,RMVar_hsa_circ_77802,RMVar_hsa_circ_98181,RMVar_hsa_circ_215793,RMVar_hsa_circ_215794,RMVar_hsa_circ_304597,RMVar_hsa_circ_292652,RMVar_hsa_circ_10723,RMVar_hsa_circ_93917,RMVar_hsa_circ_105425,RMVar_hsa_circ_85383,RMVar_hsa_circ_215798,RMVar_hsa_circ_215799,RMVar_hsa_circ_215797,RMVar_hsa_circ_82790,RMVar_hsa_circ_48326,RMVar_hsa_circ_215795,RMVar_hsa_circ_288612,RMVar_hsa_circ_341040,RMVar_hsa_circ_115249,RMVar_hsa_circ_215806,RMVar_hsa_circ_215808,RMVar_hsa_circ_215809,RMVar_hsa_circ_215807 4026 RMVar_ID_4026 Human_SNP_ID_122475660 A-to-I Human chr3 + 10078842 10078842 10078842 AAAAAGAACTAGCCGGGCATGGTGGTGCAGCTATAGTTCCAGCTACTTGGGAGGCTGAGGCATGG AAAAAGAACTAGCCGGGCATGGTGGTGCAGCTGTAGTTCCAGCTACTTGGGAGGCTGAGGCATGG A G FANCD2 Ensembl:ENSG00000144554 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs981751213 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123116,RMVar_hsa_circ_215754,RMVar_hsa_circ_80013,RMVar_hsa_circ_215758,RMVar_hsa_circ_120008,RMVar_hsa_circ_215764,RMVar_hsa_circ_117723,RMVar_hsa_circ_215766,RMVar_hsa_circ_127017,RMVar_hsa_circ_215767,RMVar_hsa_circ_119841,RMVar_hsa_circ_124318,RMVar_hsa_circ_215771,RMVar_hsa_circ_92781,RMVar_hsa_circ_215779,RMVar_hsa_circ_55648,RMVar_hsa_circ_215778,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,RMVar_hsa_circ_94327,RMVar_hsa_circ_78921,RMVar_hsa_circ_112809,RMVar_hsa_circ_215783,RMVar_hsa_circ_376157,RMVar_hsa_circ_215787,RMVar_hsa_circ_215788,RMVar_hsa_circ_89275,RMVar_hsa_circ_215789,RMVar_hsa_circ_215790,RMVar_hsa_circ_115110,RMVar_hsa_circ_215791,RMVar_hsa_circ_215796,RMVar_hsa_circ_77802,RMVar_hsa_circ_98181,RMVar_hsa_circ_215793,RMVar_hsa_circ_215794,RMVar_hsa_circ_304597,RMVar_hsa_circ_292652,RMVar_hsa_circ_10723,RMVar_hsa_circ_93917,RMVar_hsa_circ_105425,RMVar_hsa_circ_85383,RMVar_hsa_circ_215798,RMVar_hsa_circ_215799,RMVar_hsa_circ_215797,RMVar_hsa_circ_82790,RMVar_hsa_circ_48326,RMVar_hsa_circ_215795,RMVar_hsa_circ_288612,RMVar_hsa_circ_341040,RMVar_hsa_circ_115249,RMVar_hsa_circ_215806,RMVar_hsa_circ_215808,RMVar_hsa_circ_215809,RMVar_hsa_circ_215807 4027 RMVar_ID_4027 Human_SNP_ID_122475661 A-to-I Human chr3 + 10078844 10078844 10078844 AAAGAACTAGCCGGGCATGGTGGTGCAGCTATAGTTCCAGCTACTTGGGAGGCTGAGGCATGGGG AAAGAACTAGCCGGGCATGGTGGTGCAGCTATGGTTCCAGCTACTTGGGAGGCTGAGGCATGGGG A G FANCD2 Ensembl:ENSG00000144554 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1011815244 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123116,RMVar_hsa_circ_215754,RMVar_hsa_circ_80013,RMVar_hsa_circ_215758,RMVar_hsa_circ_120008,RMVar_hsa_circ_215764,RMVar_hsa_circ_117723,RMVar_hsa_circ_215766,RMVar_hsa_circ_127017,RMVar_hsa_circ_215767,RMVar_hsa_circ_119841,RMVar_hsa_circ_124318,RMVar_hsa_circ_215771,RMVar_hsa_circ_92781,RMVar_hsa_circ_215779,RMVar_hsa_circ_55648,RMVar_hsa_circ_215778,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,RMVar_hsa_circ_94327,RMVar_hsa_circ_78921,RMVar_hsa_circ_112809,RMVar_hsa_circ_215783,RMVar_hsa_circ_376157,RMVar_hsa_circ_215787,RMVar_hsa_circ_215788,RMVar_hsa_circ_89275,RMVar_hsa_circ_215789,RMVar_hsa_circ_215790,RMVar_hsa_circ_115110,RMVar_hsa_circ_215791,RMVar_hsa_circ_215796,RMVar_hsa_circ_77802,RMVar_hsa_circ_98181,RMVar_hsa_circ_215793,RMVar_hsa_circ_215794,RMVar_hsa_circ_304597,RMVar_hsa_circ_292652,RMVar_hsa_circ_10723,RMVar_hsa_circ_93917,RMVar_hsa_circ_105425,RMVar_hsa_circ_85383,RMVar_hsa_circ_215798,RMVar_hsa_circ_215799,RMVar_hsa_circ_215797,RMVar_hsa_circ_82790,RMVar_hsa_circ_48326,RMVar_hsa_circ_215795,RMVar_hsa_circ_288612,RMVar_hsa_circ_341040,RMVar_hsa_circ_115249,RMVar_hsa_circ_215806,RMVar_hsa_circ_215808,RMVar_hsa_circ_215809,RMVar_hsa_circ_215807 4028 RMVar_ID_4028 Human_SNP_ID_122475731 A-to-I Human chr3 + 10079105 10079105 10079105 TCTACTAAAAATACAAAAAAAATTAGCCAGGTATGGTGGCGCATGCTTGTAGTCCCAGGTACTTG TCTACTAAAAATACAAAAAAAATTAGCCAGGTGTGGTGGCGCATGCTTGTAGTCCCAGGTACTTG A G FANCD2 Ensembl:ENSG00000144554 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs545327078 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123116,RMVar_hsa_circ_215754,RMVar_hsa_circ_80013,RMVar_hsa_circ_215758,RMVar_hsa_circ_120008,RMVar_hsa_circ_215764,RMVar_hsa_circ_117723,RMVar_hsa_circ_215766,RMVar_hsa_circ_127017,RMVar_hsa_circ_215767,RMVar_hsa_circ_119841,RMVar_hsa_circ_124318,RMVar_hsa_circ_215771,RMVar_hsa_circ_92781,RMVar_hsa_circ_215779,RMVar_hsa_circ_55648,RMVar_hsa_circ_215778,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,RMVar_hsa_circ_94327,RMVar_hsa_circ_78921,RMVar_hsa_circ_112809,RMVar_hsa_circ_215783,RMVar_hsa_circ_376157,RMVar_hsa_circ_215787,RMVar_hsa_circ_215788,RMVar_hsa_circ_89275,RMVar_hsa_circ_215789,RMVar_hsa_circ_215790,RMVar_hsa_circ_115110,RMVar_hsa_circ_215791,RMVar_hsa_circ_215796,RMVar_hsa_circ_77802,RMVar_hsa_circ_98181,RMVar_hsa_circ_215793,RMVar_hsa_circ_215794,RMVar_hsa_circ_304597,RMVar_hsa_circ_292652,RMVar_hsa_circ_10723,RMVar_hsa_circ_93917,RMVar_hsa_circ_105425,RMVar_hsa_circ_85383,RMVar_hsa_circ_215798,RMVar_hsa_circ_215799,RMVar_hsa_circ_215797,RMVar_hsa_circ_82790,RMVar_hsa_circ_48326,RMVar_hsa_circ_215795,RMVar_hsa_circ_288612,RMVar_hsa_circ_341040,RMVar_hsa_circ_115249,RMVar_hsa_circ_215806,RMVar_hsa_circ_215808,RMVar_hsa_circ_215809,RMVar_hsa_circ_215807 4029 RMVar_ID_4029 Human_SNP_ID_122476110 A-to-I Human chr3 + 10080521 10080521 10080521 GGCAGGGCACAGTGGCTCACGCCTTTAACCCCAACACTTTGGGAGTCCAAGATGGGTGGATTGCT GGCAGGGCACAGTGGCTCACGCCTTTAACCCCCACACTTTGGGAGTCCAAGATGGGTGGATTGCT A C FANCD2 Ensembl:ENSG00000144554 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1325474052 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123116,RMVar_hsa_circ_215754,RMVar_hsa_circ_80013,RMVar_hsa_circ_215758,RMVar_hsa_circ_120008,RMVar_hsa_circ_215764,RMVar_hsa_circ_117723,RMVar_hsa_circ_215766,RMVar_hsa_circ_127017,RMVar_hsa_circ_215767,RMVar_hsa_circ_119841,RMVar_hsa_circ_124318,RMVar_hsa_circ_215771,RMVar_hsa_circ_92781,RMVar_hsa_circ_215779,RMVar_hsa_circ_55648,RMVar_hsa_circ_215778,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,RMVar_hsa_circ_94327,RMVar_hsa_circ_78921,RMVar_hsa_circ_112809,RMVar_hsa_circ_215783,RMVar_hsa_circ_376157,RMVar_hsa_circ_215787,RMVar_hsa_circ_215788,RMVar_hsa_circ_89275,RMVar_hsa_circ_215789,RMVar_hsa_circ_215790,RMVar_hsa_circ_115110,RMVar_hsa_circ_215791,RMVar_hsa_circ_215796,RMVar_hsa_circ_77802,RMVar_hsa_circ_98181,RMVar_hsa_circ_215793,RMVar_hsa_circ_215794,RMVar_hsa_circ_304597,RMVar_hsa_circ_292652,RMVar_hsa_circ_10723,RMVar_hsa_circ_93917,RMVar_hsa_circ_105425,RMVar_hsa_circ_85383,RMVar_hsa_circ_215798,RMVar_hsa_circ_215799,RMVar_hsa_circ_215797,RMVar_hsa_circ_82790,RMVar_hsa_circ_48326,RMVar_hsa_circ_215795,RMVar_hsa_circ_288612,RMVar_hsa_circ_341040,RMVar_hsa_circ_115249,RMVar_hsa_circ_215806,RMVar_hsa_circ_215808,RMVar_hsa_circ_215809,RMVar_hsa_circ_215807 4030 RMVar_ID_4030 Human_SNP_ID_122478383 A-to-I Human chr3 + 10089103 10089103 10089103 GTCAGGAGTTTTGAGACCCACTTGGCCAACATAGTGAAACCCTGTCCCTACTAAAAATACAAAAA GTCAGGAGTTTTGAGACCCACTTGGCCAACATCGTGAAACCCTGTCCCTACTAAAAATACAAAAA A C FANCD2 Ensembl:ENSG00000144554 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1204450505 Functional Loss SNV 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_77302,RMVar_hsa_circ_215781,RMVar_hsa_circ_265956,RMVar_hsa_circ_215782,RMVar_hsa_circ_94327,RMVar_hsa_circ_78921,RMVar_hsa_circ_112809,RMVar_hsa_circ_215783,RMVar_hsa_circ_215788,RMVar_hsa_circ_89275,RMVar_hsa_circ_215789,RMVar_hsa_circ_215790,RMVar_hsa_circ_115110,RMVar_hsa_circ_215791,RMVar_hsa_circ_215796,RMVar_hsa_circ_304597,RMVar_hsa_circ_10723,RMVar_hsa_circ_93917,RMVar_hsa_circ_215795,RMVar_hsa_circ_115249,RMVar_hsa_circ_119367,RMVar_hsa_circ_215806,RMVar_hsa_circ_123801,RMVar_hsa_circ_215812,RMVar_hsa_circ_55591,RMVar_hsa_circ_103351,RMVar_hsa_circ_215814,RMVar_hsa_circ_215815,RMVar_hsa_circ_95112,RMVar_hsa_circ_215816 4031 RMVar_ID_4031 Human_SNP_ID_122486093 A-to-I Human chr3 + 10116971 10116971 10116971 GGGTGTTTAGGACTATAATCGTGGCTGAGTTCAATGGCTTATGTCTGTAATCCCAGCACTTTGGG GGGTGTTTAGGACTATAATCGTGGCTGAGTTCCATGGCTTATGTCTGTAATCCCAGCACTTTGGG A C BRK1 Ensembl:ENSG00000254999 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1304169718 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82252,RMVar_hsa_circ_215819 4032 RMVar_ID_4032 Human_SNP_ID_122486498 A-to-I Human chr3 + 10118627 10118627 10118627 TTCTTGGCTTAGCTTCCTGAGTAGCTGGGACTACAGGTGTGTGCCACCATGCCCGGCTAATATTT TTCTTGGCTTAGCTTCCTGAGTAGCTGGGACTGCAGGTGTGTGCCACCATGCCCGGCTAATATTT A G BRK1 Ensembl:ENSG00000254999 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs532114750 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82252,RMVar_hsa_circ_215819 4033 RMVar_ID_4033 Human_SNP_ID_122487357 A-to-I Human chr3 + 10122157 10122157 10122157 TGTTGGTCAGGTTTGTCTTGAACTCCGACCTCAGGTGATCCGCCCGCCTCGGCCTCCCAAAGTGC TGTTGGTCAGGTTTGTCTTGAACTCCGACCTCGGGTGATCCGCCCGCCTCGGCCTCCCAAAGTGC A G BRK1 Ensembl:ENSG00000254999 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978825545 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82252,RMVar_hsa_circ_215819 4034 RMVar_ID_4034 Human_SNP_ID_122487358 A-to-I Human chr3 + 10122157 10122157 10122157 TGTTGGTCAGGTTTGTCTTGAACTCCGACCTCAGGTGATCCGCCCGCCTCGGCCTCCCAAAGTGC TGTTGGTCAGGTTTGTCTTGAACTCCGACCTCTGGTGATCCGCCCGCCTCGGCCTCCCAAAGTGC A T BRK1 Ensembl:ENSG00000254999 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978825545 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82252,RMVar_hsa_circ_215819 4035 RMVar_ID_4035 Human_SNP_ID_122487874 A-to-I Human chr3 + 10123996 10123996 10123996 ACCTCAGTTGATCTGCCCACCTTGGCTTCCCAAAGTGCTGGGATTACAGGCGTGAGCCATCACGC ACCTCAGTTGATCTGCCCACCTTGGCTTCCCAGAGTGCTGGGATTACAGGCGTGAGCCATCACGC A G BRK1 Ensembl:ENSG00000254999 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1559420062 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82252,RMVar_hsa_circ_215819 4036 RMVar_ID_4036 Human_SNP_ID_122494105 A-to-I Human chr3 + 10143547 10143546 10143548 TTGGCTCACTGCAATCTCCGACTCCCTGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAAC TTGGCTCACTGCAATCTCCGACTCCCTGGTTC__GCGATTCTCCTGCCTCAGCCTCCCAAGTAAC CAA C VHL Ensembl:ENSG00000134086 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1463348984 Functional Loss DEL dbSNP153 33..34 33 - - - 4037 RMVar_ID_4037 Human_SNP_ID_122494129 A-to-I Human chr3 + 10143623 10143623 10143623 GCACGCACTACCATTCCCAGCTAATTTTTTGTATTCTTAGTAGAGACAGGGTTTCACCATGTTGG GCACGCACTACCATTCCCAGCTAATTTTTTGTGTTCTTAGTAGAGACAGGGTTTCACCATGTTGG A G VHL Ensembl:ENSG00000134086 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1371082775 Functional Loss SNV dbSNP153 33..33 33 - - - 4038 RMVar_ID_4038 Human_SNP_ID_122494289 A-to-I Human chr3 + 10144241 10144241 10144241 GTGATCTCAGCACTTTGGGAGGCTGAGGCAGGAGGATTTCTTGAGCCCAGGAGCTGGAGACCAGC GTGATCTCAGCACTTTGGGAGGCTGAGGCAGGCGGATTTCTTGAGCCCAGGAGCTGGAGACCAGC A C VHL Ensembl:ENSG00000134086 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1425196249 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14554250 4039 RMVar_ID_4039 Human_SNP_ID_122494290 A-to-I Human chr3 + 10144241 10144241 10144241 GTGATCTCAGCACTTTGGGAGGCTGAGGCAGGAGGATTTCTTGAGCCCAGGAGCTGGAGACCAGC GTGATCTCAGCACTTTGGGAGGCTGAGGCAGGGGGATTTCTTGAGCCCAGGAGCTGGAGACCAGC A G VHL Ensembl:ENSG00000134086 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1425196249 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14554250 4040 RMVar_ID_4040 Human_SNP_ID_122494345 A-to-I Human chr3 + 10144415 10144415 10144415 GGAAGATCACCCGAACCCAGGAGTTGGAGGCTACAGTGAACTATGATGGTGCCTCTGAATAGTTG GGAAGATCACCCGAACCCAGGAGTTGGAGGCTGCAGTGAACTATGATGGTGCCTCTGAATAGTTG A G VHL Ensembl:ENSG00000134086 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs533914115 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14554256 4041 RMVar_ID_4041 Human_SNP_ID_122494346 A-to-I Human chr3 + 10144415 10144415 10144415 GGAAGATCACCCGAACCCAGGAGTTGGAGGCTACAGTGAACTATGATGGTGCCTCTGAATAGTTG GGAAGATCACCCGAACCCAGGAGTTGGAGGCTTCAGTGAACTATGATGGTGCCTCTGAATAGTTG A T VHL Ensembl:ENSG00000134086 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs533914115 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14554256 4042 RMVar_ID_4042 Human_SNP_ID_122495543 A-to-I Human chr3 + 10147908 10147908 10147908 GAGACCAGGAGTTCTTGACCAGCCTGGACAACAAAGTGAGACCCCAGCTCCACAAAAAAATTTTT GAGACCAGGAGTTCTTGACCAGCCTGGACAACCAAGTGAGACCCCAGCTCCACAAAAAAATTTTT A C VHL Ensembl:ENSG00000134086 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs947937400 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14554376,Human_RBP_ID_18793195 4043 RMVar_ID_4043 Human_SNP_ID_122496026 A-to-I Human chr3 + 10149182 10149182 10149182 TCACCCAGGTTGGAGTGCAGTGGCATGATCTTAGCTCACTGCAACCTCTGCCTCCAGGGCTCAAG TCACCCAGGTTGGAGTGCAGTGGCATGATCTTGGCTCACTGCAACCTCTGCCTCCAGGGCTCAAG A G VHL Ensembl:ENSG00000134086 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs531383130 Functional Loss SNV dbSNP153 33..33 33 - - - 4044 RMVar_ID_4044 Human_SNP_ID_122496057 A-to-I Human chr3 + 10149297 10149297 10149297 ACCATGCCTGGCTAATTTTTTGTGTATTTTGTAGAGACGGGGTTTCGCCATGTTGCCAGGCTGGT ACCATGCCTGGCTAATTTTTTGTGTATTTTGTGGAGACGGGGTTTCGCCATGTTGCCAGGCTGGT A G VHL Ensembl:ENSG00000134086 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs530154637 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14554411 4045 RMVar_ID_4045 Human_SNP_ID_122496675 A-to-I Human chr3 + 10151020 10151020 10151020 GGTTCACGTAATCCTCCTGAGTAGCTGGGATTACAGGCGCCTGCCACCACGCTGGCCAATTTTTG GGTTCACGTAATCCTCCTGAGTAGCTGGGATTGCAGGCGCCTGCCACCACGCTGGCCAATTTTTG A G VHL Ensembl:ENSG00000134086 Protein coding 3'UTR GSE38233;GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,32596459,32596459 RNA-Seq:(High) rs1459644379 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_266488,Human_RBP_ID_9128880,Human_RBP_ID_26510035 Human_miRNA_ID_1400122 4046 RMVar_ID_4046 Human_SNP_ID_122496688 A-to-I Human chr3 + 10151045 10151045 10151045 TGGGATTACAGGCGCCTGCCACCACGCTGGCCAATTTTTGTACTTTTAGTAGAGACAGTGTTTCG TGGGATTACAGGCGCCTGCCACCACGCTGGCCCATTTTTGTACTTTTAGTAGAGACAGTGTTTCG A C VHL Ensembl:ENSG00000134086 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs998300782 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14554525,Human_RBP_ID_26510036 Human_miRNA_ID_878907,Human_miRNA_ID_1811768 4047 RMVar_ID_4047 Human_SNP_ID_122496692 A-to-I Human chr3 + 10151060 10151056 10151060 CTGCCACCACGCTGGCCAATTTTTGTACTTTTAGTAGAGACAGTGTTTCGTCATGTTGGCCAGGC CTGCCACCACGCTGGCCAATTTTTGTACT____GTAGAGACAGTGTTTCGTCATGTTGGCCAGGC TTTTA T VHL Ensembl:ENSG00000134086 Protein coding 3'UTR GSE38233;GSE99789 cultured B-cells;esophageal squamous carcinoma cells,EC109 - 24183664,29796672 RNA-Seq:(High) rs1168010331 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_14554525 Human_miRNA_ID_1433817 4048 RMVar_ID_4048 Human_SNP_ID_122496714 A-to-I Human chr3 + 10151141 10151141 10151141 ACCTCAGGTGATCCGCCCACCTCAGCCTCCCAAAATGGTGGGATTACAGGTGTGTGGGCCACCGT ACCTCAGGTGATCCGCCCACCTCAGCCTCCCAGAATGGTGGGATTACAGGTGTGTGGGCCACCGT A G VHL Ensembl:ENSG00000134086 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs981311820 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7241911,Human_RBP_ID_14554528,Human_RBP_ID_26511622 4049 RMVar_ID_4049 Human_SNP_ID_122496892 A-to-I Human chr3 + 10151791 10151791 10151791 TCCTGTGCTCAAAAATGAGAGTGACGGCTGGCATGGTGGCTCCCGCCTGTAATCCCAGTACTTTG TCCTGTGCTCAAAAATGAGAGTGACGGCTGGCGTGGTGGCTCCCGCCTGTAATCCCAGTACTTTG A G VHL Ensembl:ENSG00000134086 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1058854 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_584662,Human_RBP_ID_7099667,Human_RBP_ID_8209615,Human_RBP_ID_9128882,Human_RBP_ID_14554578,Human_RBP_ID_17574237,Human_RBP_ID_23956866,Human_RBP_ID_26510048 4050 RMVar_ID_4050 Human_SNP_ID_122496902 A-to-I Human chr3 + 10151836 10151836 10151836 CCTGTAATCCCAGTACTTTGGAAAGCCAAGGTAAGAGGATTGCTTGAGCCCAGAACTTCAAGATG CCTGTAATCCCAGTACTTTGGAAAGCCAAGGTGAGAGGATTGCTTGAGCCCAGAACTTCAAGATG A G VHL Ensembl:ENSG00000134086 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037405675 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_584663,Human_RBP_ID_4715775,Human_RBP_ID_7099669,Human_RBP_ID_14554587,Human_RBP_ID_17990411,Human_RBP_ID_18330916,Human_RBP_ID_26510049,Human_RBP_ID_26762901 4051 RMVar_ID_4051 Human_SNP_ID_122496903 A-to-I Human chr3 + 10151836 10151836 10151836 CCTGTAATCCCAGTACTTTGGAAAGCCAAGGTAAGAGGATTGCTTGAGCCCAGAACTTCAAGATG CCTGTAATCCCAGTACTTTGGAAAGCCAAGGTTAGAGGATTGCTTGAGCCCAGAACTTCAAGATG A T VHL Ensembl:ENSG00000134086 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037405675 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_584663,Human_RBP_ID_4715775,Human_RBP_ID_7099669,Human_RBP_ID_14554587,Human_RBP_ID_17990411,Human_RBP_ID_18330916,Human_RBP_ID_26510049,Human_RBP_ID_26762901 4052 RMVar_ID_4052 Human_SNP_ID_122496925 A-to-I Human chr3 + 10151922 10151922 10151922 CCCATCTATACAAAAAATTTTTAAAAATTAGCATGGCGGCACACATCTGTAATCCTAGCTACTTG CCCATCTATACAAAAAATTTTTAAAAATTAGCGTGGCGGCACACATCTGTAATCCTAGCTACTTG A G VHL Ensembl:ENSG00000134086 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs964125414 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_584665,Human_RBP_ID_4715778,Human_RBP_ID_7099675,Human_RBP_ID_8209616,Human_RBP_ID_14554594,Human_RBP_ID_17574004,Human_RBP_ID_17990413,Human_RBP_ID_22371895,Human_RBP_ID_23188175,Human_RBP_ID_23312183,Human_RBP_ID_26501879 4053 RMVar_ID_4053 Human_SNP_ID_122497025 A-to-I Human chr3 + 10152189 10152189 10152189 CAGGAGTTCGAGACCAGCCTGGCCAACATGGTAAAACCCCATTTCTACTAAAAAATACAAGAATT CAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCCATTTCTACTAAAAAATACAAGAATT A G VHL Ensembl:ENSG00000134086 Protein coding 3'UTR GSE38233;GSE100210;GSE99789;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,29796672,29796672,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs886057734 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17990414,Human_RBP_ID_27709790 Clinvar_Rec_30,Clinvar_Rec_166 4054 RMVar_ID_4054 Human_SNP_ID_122497029 A-to-I Human chr3 + 10152222 10152222 10152222 AAACCCCATTTCTACTAAAAAATACAAGAATTAGCTGGGTGTGGTGGCGCATGCCTGTAATCCTA AAACCCCATTTCTACTAAAAAATACAAGAATTGGCTGGGTGTGGTGGCGCATGCCTGTAATCCTA A G VHL Ensembl:ENSG00000134086 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1136254 Functional Loss SNV dbSNP153 33..33 33 - - - 4055 RMVar_ID_4055 Human_SNP_ID_122497062 A-to-I Human chr3 + 10152351 10152351 10152351 ATATCGCACCATTGTACTCCAGCCTGTGTGACAGAGCAATACTCTTGTCTCAAAAAAAAAAAAAA ATATCGCACCATTGTACTCCAGCCTGTGTGACCGAGCAATACTCTTGTCTCAAAAAAAAAAAAAA A C VHL Ensembl:ENSG00000134086 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs967946710 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_584669,Human_RBP_ID_7099681,Human_RBP_ID_23188180 4056 RMVar_ID_4056 Human_SNP_ID_122497151 A-to-I Human chr3 + 10152570 10152570 10152570 GCTGGAGTGCAGTGGTGCGATCTCTGCTCACTACAAGCTCTGCCTCCCGAGTTCAAGTGATTCTC GCTGGAGTGCAGTGGTGCGATCTCTGCTCACTGCAAGCTCTGCCTCCCGAGTTCAAGTGATTCTC A G VHL Ensembl:ENSG00000134086 Protein coding 3'UTR GSE38233;GSE100210;GSE99789 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 24183664,29129909,29796672 RNA-Seq:(High) rs1325969275 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26501886 4057 RMVar_ID_4057 Human_SNP_ID_122497181 A-to-I Human chr3 + 10152672 10152672 10152672 CTGCCACCATGCCTGGCTAATTTTGTGTTTTTAGTGGAGACGGGGTTTCACCATGTTGTCCAGGA CTGCCACCATGCCTGGCTAATTTTGTGTTTTTTGTGGAGACGGGGTTTCACCATGTTGTCCAGGA A T VHL Ensembl:ENSG00000134086 Protein coding 3'UTR GSE38233;GSE100210;GSE99789;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,29796672,32596459,32596459 RNA-Seq:(High) rs1244549737 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_584675,Human_RBP_ID_4715790 4058 RMVar_ID_4058 Human_SNP_ID_122497202 A-to-I Human chr3 + 10152742 10152742 10152742 TTGATCTCCTGACCTTGTGATCCACCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG TTGATCTCCTGACCTTGTGATCCACCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG A G VHL Ensembl:ENSG00000134086 Protein coding 3'UTR GSE38233;GSE99789 cultured B-cells;esophageal squamous carcinoma cells,EC109 - 24183664,29796672 RNA-Seq:(High) rs915120070 Functional Loss SNV dbSNP153 33..33 33 - - - 4059 RMVar_ID_4059 Human_SNP_ID_122497208 A-to-I Human chr3 + 10152764 10152764 10152764 CACCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCGTCCAGCCAGCTTTA CACCCACCTCAGCCTCCCAAAGTGCTGGGATTGCAGGTGTGAGCCACCGCGTCCAGCCAGCTTTA A G VHL Ensembl:ENSG00000134086 Protein coding 3'UTR GSE38233;GSE100210;GSE99789;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,29796672,32596459 RNA-Seq:(High) rs1335663958 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23188188 4060 RMVar_ID_4060 Human_SNP_ID_122497243 A-to-I Human chr3 + 10152879 10152874 10152880 TGTTAAAACCTGCAGGCCGAGCACAGTGGCTCATGCCTGTAATCCCAGCATTTTGGGAGACCAAG TGTTAAAACCTGCAGGCCGAGCACAGTG______GCCTGTAATCCCAGCATTTTGGGAGACCAAG GGCTCAT G VHL Ensembl:ENSG00000134086 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1364700572 Functional Loss DEL dbSNP153 29..34 33 - - - Human_RBP_ID_23188192 4061 RMVar_ID_4061 Human_SNP_ID_122497310 A-to-I Human chr3 + 10153057 10153057 10153057 CCAGCACTTTGGGAGGCCTAGGCGGGTGGATCACGAGGTCAGGAAATCGAGACCATCCTGGCTAA CCAGCACTTTGGGAGGCCTAGGCGGGTGGATCGCGAGGTCAGGAAATCGAGACCATCCTGGCTAA A G VHL Ensembl:ENSG00000134086 Protein coding 3'UTR GSE47997;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,32596459 RNA-Seq:(High) rs1026556299 Functional Loss SNV dbSNP153 33..33 33 - - - 4062 RMVar_ID_4062 Human_SNP_ID_122497315 A-to-I Human chr3 + 10153065 10153065 10153065 TTGGGAGGCCTAGGCGGGTGGATCACGAGGTCAGGAAATCGAGACCATCCTGGCTAACACGGGTG TTGGGAGGCCTAGGCGGGTGGATCACGAGGTCGGGAAATCGAGACCATCCTGGCTAACACGGGTG A G VHL Ensembl:ENSG00000134086 Protein coding 3'UTR GSE47997;GSE38233;GSE107867;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;ASD brains,frontal_cortex;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,30559470,32596459 RNA-Seq:(High) rs1405404507 Functional Loss SNV dbSNP153 33..33 33 - - - 4063 RMVar_ID_4063 Human_SNP_ID_122497322 A-to-I Human chr3 + 10153088 10153088 10153088 CACGAGGTCAGGAAATCGAGACCATCCTGGCTAACACGGGTGAAACCCCGTCTCTATTAAAAAAT CACGAGGTCAGGAAATCGAGACCATCCTGGCTGACACGGGTGAAACCCCGTCTCTATTAAAAAAT A G VHL Ensembl:ENSG00000134086 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1018699364 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23188198 4064 RMVar_ID_4064 Human_SNP_ID_122497345 A-to-I Human chr3 + 10153167 10153167 10153167 GGGCGTGGTGGTGAGCGCCTGTAGTCCCAGCTACTCGAGAGCCTGAGGCAGGAGAATGGCATGAA GGGCGTGGTGGTGAGCGCCTGTAGTCCCAGCTGCTCGAGAGCCTGAGGCAGGAGAATGGCATGAA A G VHL Ensembl:ENSG00000134086 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1362807922 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_584677,Human_RBP_ID_14554632,Human_RBP_ID_23312185 4065 RMVar_ID_4065 Human_SNP_ID_122497398 A-to-I Human chr3 + 10153304 10153304 10153304 CGTCTCAAAAAAAAAAACAAAAAACAAAAATTATCCAGGTGTGGCGGTGGGCGCCTGTGAGGCAG CGTCTCAAAAAAAAAAACAAAAAACAAAAATTGTCCAGGTGTGGCGGTGGGCGCCTGTGAGGCAG A G VHL Ensembl:ENSG00000134086 Protein coding 3'UTR GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459,32596459 RNA-Seq:(High) rs1046330641 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_584679,Human_RBP_ID_17990423,Human_RBP_ID_23188204,Human_RBP_ID_26501900,Human_RBP_ID_27042063 4066 RMVar_ID_4066 Human_SNP_ID_122497427 A-to-I Human chr3 + 10153386 10153386 10153386 GGGAGGCGGAGGTTGCAGTGAGCCAAGATCACACCATTGCACTCCAGCCTGGGCAACAAGAGTGA GGGAGGCGGAGGTTGCAGTGAGCCAAGATCACGCCATTGCACTCCAGCCTGGGCAACAAGAGTGA A G VHL Ensembl:ENSG00000134086 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1008891698 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4715811,Human_RBP_ID_10113896,Human_RBP_ID_25765459 4067 RMVar_ID_4067 Human_SNP_ID_122497432 A-to-I Human chr3 + 10153411 10153410 10153412 AGATCACACCATTGCACTCCAGCCTGGGCAACAAGAGTGAAATTCCATCTCAAAAAGAAACCAAA AGATCACACCATTGCACTCCAGCCTGGGCAAC__GAGTGAAATTCCATCTCAAAAAGAAACCAAA CAA C VHL Ensembl:ENSG00000134086 Protein coding 3'UTR GSE38233;GSE100210;GSE99789 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 24183664,29129909,29796672 RNA-Seq:(High) rs1441667548 Functional Loss DEL dbSNP153 33..34 33 - - - 4068 RMVar_ID_4068 Human_SNP_ID_122497433 A-to-I Human chr3 + 10153418 10153418 10153418 ACCATTGCACTCCAGCCTGGGCAACAAGAGTGAAATTCCATCTCAAAAAGAAACCAAAAAAACAA ACCATTGCACTCCAGCCTGGGCAACAAGAGTGGAATTCCATCTCAAAAAGAAACCAAAAAAACAA A G VHL Ensembl:ENSG00000134086 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs140044688 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_31,Clinvar_Rec_32 4069 RMVar_ID_4069 Human_SNP_ID_122504768 A-to-I Human chr3 + 10177378 10177378 10177378 GAAGATGAGCGCCTCCTGCATTTTCCTTCCCTAGGTGCCTCACCTGACTCACCCTCATCCTGGCC GAAGATGAGCGCCTCCTGCATTTTCCTTCCCTGGGTGCCTCACCTGACTCACCCTCATCCTGGCC A G IRAK2 Ensembl:ENSG00000134070 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs377085311 Functional Loss SNV dbSNP153 33..33 33 - - - 4070 RMVar_ID_4070 Human_SNP_ID_122505229 A-to-I Human chr3 + 10178941 10178941 10178941 CTCCTGCCTCAACTTCCTGAGTAATTGGGACTATAGGCACATGCCACCATGCCTGACTAATTTTT CTCCTGCCTCAACTTCCTGAGTAATTGGGACTGTAGGCACATGCCACCATGCCTGACTAATTTTT A G IRAK2 Ensembl:ENSG00000134070 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs979217439 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57864,RMVar_hsa_circ_354447 4071 RMVar_ID_4071 Human_SNP_ID_122512079 A-to-I Human chr3 + 10204704 10204704 10204704 CTGGGAGGCGGAGGTTGCAGTGAGCCGAGATCACGCCACTGCACTCCAGCTTGGGTGACAGAGAA CTGGGAGGCGGAGGTTGCAGTGAGCCGAGATCGCGCCACTGCACTCCAGCTTGGGTGACAGAGAA A G IRAK2 Ensembl:ENSG00000134070 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs777217186 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55231,RMVar_hsa_circ_57864,RMVar_hsa_circ_354447,RMVar_hsa_circ_337287,RMVar_hsa_circ_362763,RMVar_hsa_circ_368139,RMVar_hsa_circ_356715,RMVar_hsa_circ_323365,RMVar_hsa_circ_215822 4072 RMVar_ID_4072 Human_SNP_ID_122526516 A-to-I Human chr3 + 10255135 10255135 10255135 TGGCTCAGGTGATCTTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCGTGCACCACCATG TGGCTCAGGTGATCTTCCTGCCTCAGCCTCCCCAGTAGCTGGGACTACAGGCGTGCACCACCATG A C TATDN2,AC022384.1 Ensembl:ENSG00000157014,Ensembl:ENSG00000272410 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1418296453 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_215827,RMVar_hsa_circ_101231 4073 RMVar_ID_4073 Human_SNP_ID_122531407 A-to-I Human chr3 + 10272538 10272538 10272538 TTGGCTCACTGCAGCCTCCAGTTCCCAGGTTCAAGCGATTCTCTTGCCTCAGCCTCCTGAGTAGC TTGGCTCACTGCAGCCTCCAGTTCCCAGGTTCCAGCGATTCTCTTGCCTCAGCCTCCTGAGTAGC A C TATDN2,AC022384.1 Ensembl:ENSG00000157014,Ensembl:ENSG00000272410 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1421659376 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_215827,RMVar_hsa_circ_101231,RMVar_hsa_circ_334876 4074 RMVar_ID_4074 Human_SNP_ID_122532029 A-to-I Human chr3 + 10275079 10275079 10275079 ATGATCTCAGCTCACTGCAGCCTTTGCCTCCCAGGTTCAGGGGATTCTCCTGCCTCAGCCACCCA ATGATCTCAGCTCACTGCAGCCTTTGCCTCCCGGGTTCAGGGGATTCTCCTGCCTCAGCCACCCA A G TATDN2,AC022384.1 Ensembl:ENSG00000157014,Ensembl:ENSG00000272410 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1006162486 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_215827,RMVar_hsa_circ_101231,RMVar_hsa_circ_334876 4075 RMVar_ID_4075 Human_SNP_ID_122533843 A-to-I Human chr3 + 10281494 10281494 10281494 GGGATTACAGGTGCCTGCCACCGTGCCCGGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTC GGGATTACAGGTGCCTGCCACCGTGCCCGGCTGATTTTTTGTATTTTTAGTAGAGACGGGGTTTC A G AC022384.1 Ensembl:ENSG00000272410 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs950668781 Functional Loss SNV dbSNP153 33..33 33 - - - 4076 RMVar_ID_4076 Human_SNP_ID_122533847 A-to-I Human chr3 + 10281510 10281510 10281510 GCCACCGTGCCCGGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCGTGTTAACCAAGA GCCACCGTGCCCGGCTAATTTTTTGTATTTTTTGTAGAGACGGGGTTTCACCGTGTTAACCAAGA A T AC022384.1 Ensembl:ENSG00000272410 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1307580988 Functional Loss SNV dbSNP153 33..33 33 - - - 4077 RMVar_ID_4077 Human_SNP_ID_122533945 A-to-I Human chr3 + 10281835 10281832 10281836 GAAACCCTATTTCTACTAAAAATACAAAAACTAGCTGGGTGGGGTGGCACGCGCCTGTAGTCCCA GAAACCCTATTTCTACTAAAAATACAAAAA____CTGGGTGGGGTGGCACGCGCCTGTAGTCCCA ACTAG A AC022384.1 Ensembl:ENSG00000272410 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1345949527 Functional Loss DEL dbSNP153 31..34 33 - - - 4078 RMVar_ID_4078 Human_SNP_ID_122537618 A-to-I Human chr3 + 10293843 10293843 10293843 CTCTGTCACCCAGGCTGGAGTGCAGTGGCACTATCATGGCTCACTGCAGCCTCCACCTCCCTGGA CTCTGTCACCCAGGCTGGAGTGCAGTGGCACTCTCATGGCTCACTGCAGCCTCCACCTCCCTGGA A C GHRLOS Ensembl:ENSG00000240288 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913860056 Functional Loss SNV dbSNP153 33..33 33 - - - 4079 RMVar_ID_4079 Human_SNP_ID_122537619 A-to-I Human chr3 + 10293843 10293843 10293843 CTCTGTCACCCAGGCTGGAGTGCAGTGGCACTATCATGGCTCACTGCAGCCTCCACCTCCCTGGA CTCTGTCACCCAGGCTGGAGTGCAGTGGCACTGTCATGGCTCACTGCAGCCTCCACCTCCCTGGA A G GHRLOS Ensembl:ENSG00000240288 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913860056 Functional Loss SNV dbSNP153 33..33 33 - - - 4080 RMVar_ID_4080 Human_SNP_ID_122541508 A-to-I Human chr3 + 10306721 10306721 10306721 GGGGCAAGTCTTTCCCATGCTGTTCTCATGATAGTGAATAAGTCTCGCTAGATCTGACGATTTTA GGGGCAAGTCTTTCCCATGCTGTTCTCATGATGGTGAATAAGTCTCGCTAGATCTGACGATTTTA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334645151 Functional Loss SNV dbSNP153 33..33 33 - - - 4081 RMVar_ID_4081 Human_SNP_ID_122541517 A-to-I Human chr3 - 10306743 10306743 10306743 TGTGCAGAAAAACTCCCATTTTTAAAATCGTCAGATCTAGCGAGACTTATTCACTATCATGAGAA TGTGCAGAAAAACTCCCATTTTTAAAATCGTCCGATCTAGCGAGACTTATTCACTATCATGAGAA T G SEC13 Ensembl:ENSG00000157020 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1305880693 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118440,RMVar_hsa_circ_215834,RMVar_hsa_circ_90654,RMVar_hsa_circ_215833,RMVar_hsa_circ_321863,RMVar_hsa_circ_127072,RMVar_hsa_circ_215836 4082 RMVar_ID_4082 Human_SNP_ID_122541535 A-to-I Human chr3 + 10306807 10306807 10306807 AAGCTCTCTCTTTTGCCTGCTGCCATCCACGTAAGCTGTGACTTGTTCCTCCTTGCCTTCTGCCA AAGCTCTCTCTTTTGCCTGCTGCCATCCACGTGAGCTGTGACTTGTTCCTCCTTGCCTTCTGCCA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474806579 Functional Loss SNV dbSNP153 33..33 33 - - - 4083 RMVar_ID_4083 Human_SNP_ID_122542214 A-to-I Human chr3 - 10309023 10309023 10309023 TGAGGCAAGAGAATTGCTTGAACCCGGGAGTCAGAGGTTGCAGAGAGCCAAGATCACGCCATTAT TGAGGCAAGAGAATTGCTTGAACCCGGGAGTCCGAGGTTGCAGAGAGCCAAGATCACGCCATTAT T G SEC13 Ensembl:ENSG00000157020 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1368984031 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118440,RMVar_hsa_circ_215834,RMVar_hsa_circ_90654,RMVar_hsa_circ_215833,RMVar_hsa_circ_321863,RMVar_hsa_circ_127072,RMVar_hsa_circ_215836 4084 RMVar_ID_4084 Human_SNP_ID_122544688 A-to-I Human chr3 - 10318245 10318245 10318245 TCTTATTTGTGTCTGTATATCCAGTTCCTAGCACAGTGCTTGGCAGAAAGAAGGTACTTAGAATG TCTTATTTGTGTCTGTATATCCAGTTCCTAGCGCAGTGCTTGGCAGAAAGAAGGTACTTAGAATG T C SEC13 Ensembl:ENSG00000157020 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1559501995 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3680511,Human_RBP_ID_8554447,Human_RBP_ID_14556267 RMVar_hsa_circ_118440,RMVar_hsa_circ_215834 4085 RMVar_ID_4085 Human_SNP_ID_122573045 A-to-I Human chr3 - 10431032 10431032 10431032 CAGCAATTCACTCATATCTTCACGCTCCACTTATCTTTGGGTATCCTAACATTCCCAGTCCTATA CAGCAATTCACTCATATCTTCACGCTCCACTTGTCTTTGGGTATCCTAACATTCCCAGTCCTATA T C ATP2B2 Ensembl:ENSG00000157087 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1348644421 Functional Loss SNV dbSNP153 33..33 33 - - - 4086 RMVar_ID_4086 Human_SNP_ID_122577483 A-to-I Human chr3 - 10449534 10449534 10449534 CCCGAGCAAGGACCGCAGCAAACATGGGTGACATGACCAACAGCGACTTTTACTCCAAAAACCAA CCCGAGCAAGGACCGCAGCAAACATGGGTGACGTGACCAACAGCGACTTTTACTCCAAAAACCAA T C ATP2B2 Ensembl:ENSG00000157087 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1473080344 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_335344 4087 RMVar_ID_4087 Human_SNP_ID_122751100 A-to-I Human chr3 + 11148779 11148778 11148779 GCTGGGAAATATAATATTTTAGTTGGATATTGAGAGAATAGTTATTAAGAGACAAACCACAGTCT GCTGGGAAATATAATATTTTAGTTGGATATTG_GAGAATAGTTATTAAGAGACAAACCACAGTCT GA G HRH1 Ensembl:ENSG00000196639 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1263629681 Functional Loss DEL dbSNP153 33..33 33 - - - 4088 RMVar_ID_4088 Human_SNP_ID_122765332 A-to-I Human chr3 - 11207314 11207314 11207314 GTGATCCACCCGCCTTGGCCTCCCAAAGTGCTAGGATTACAGGCGTGGGACACCGTGCCCAGCCC GTGATCCACCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGGGACACCGTGCCCAGCCC T C AC083855.2 Ensembl:ENSG00000285906 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs998408904 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_394776,Human_Splice_Rec_394777 4089 RMVar_ID_4089 Human_SNP_ID_122767481 A-to-I Human chr3 - 11216434 11216434 11216434 ATATCACAGGATTTCCTTTCTTTTGGATGCTGAATAATATTTTATTGTATGAATACGCCACATTT ATATCACAGGATTTCCTTTCTTTTGGATGCTGGATAATATTTTATTGTATGAATACGCCACATTT T C AC083855.2 Ensembl:ENSG00000285906 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1241114737 Functional Loss SNV dbSNP153 33..33 33 - - - 4090 RMVar_ID_4090 Human_SNP_ID_122767784 A-to-I Human chr3 - 11217637 11217637 11217637 ACATTCATATTGTTGTGCAACCAATCTCCAGAACTCTCTTTATCTTGTAAAACTGAAACTCTATA ACATTCATATTGTTGTGCAACCAATCTCCAGATCTCTCTTTATCTTGTAAAACTGAAACTCTATA T A AC083855.2 Ensembl:ENSG00000285906 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1210420877 Functional Loss SNV dbSNP153 33..33 33 - - - 4091 RMVar_ID_4091 Human_SNP_ID_122767785 A-to-I Human chr3 - 11217637 11217637 11217637 ACATTCATATTGTTGTGCAACCAATCTCCAGAACTCTCTTTATCTTGTAAAACTGAAACTCTATA ACATTCATATTGTTGTGCAACCAATCTCCAGAGCTCTCTTTATCTTGTAAAACTGAAACTCTATA T C AC083855.2 Ensembl:ENSG00000285906 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1210420877 Functional Loss SNV dbSNP153 33..33 33 - - - 4092 RMVar_ID_4092 Human_SNP_ID_122768233 A-to-I Human chr3 - 11219357 11219357 11219357 TACCACTTTAACCATTTTACATGCACAGTTCAATGATACTAACTACATTCACAACCACGCAACCA TACCACTTTAACCATTTTACATGCACAGTTCAGTGATACTAACTACATTCACAACCACGCAACCA T C AC083855.2 Ensembl:ENSG00000285906 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1252065423 Functional Loss SNV dbSNP153 33..33 33 - - - 4093 RMVar_ID_4093 Human_SNP_ID_122792077 A-to-I Human chr3 + 11314828 11314813 11314828 AGCCATGGTGGTGTGTGCCTGTGGTCCCAGCTACTCAGGAGGCTGAGGTAGGAGGATTGATTGAG AGCCATGGTGGTGTGTGC_______________CTCAGGAGGCTGAGGTAGGAGGATTGATTGAG CCTGTGGTCCCAGCTA C ATG7 Ensembl:ENSG00000197548 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1446525455 Functional Loss DEL dbSNP153 19..33 33 - - - RMVar_hsa_circ_46293,RMVar_hsa_circ_109320,RMVar_hsa_circ_107817,RMVar_hsa_circ_266109,RMVar_hsa_circ_337388,RMVar_hsa_circ_87404,RMVar_hsa_circ_215852,RMVar_hsa_circ_370851,RMVar_hsa_circ_373095,RMVar_hsa_circ_375173,RMVar_hsa_circ_374631,RMVar_hsa_circ_372422,RMVar_hsa_circ_271174,RMVar_hsa_circ_277943,RMVar_hsa_circ_109613,RMVar_hsa_circ_215857,RMVar_hsa_circ_215859,RMVar_hsa_circ_215861,RMVar_hsa_circ_215862,RMVar_hsa_circ_215860,RMVar_hsa_circ_215858,RMVar_hsa_circ_215855,RMVar_hsa_circ_215856,RMVar_hsa_circ_215854,RMVar_hsa_circ_23464,RMVar_hsa_circ_309709,RMVar_hsa_circ_215865,RMVar_hsa_circ_86503,RMVar_hsa_circ_324359,RMVar_hsa_circ_215864,RMVar_hsa_circ_363254,RMVar_hsa_circ_314486,RMVar_hsa_circ_86415,RMVar_hsa_circ_306562,RMVar_hsa_circ_72294,RMVar_hsa_circ_215866,RMVar_hsa_circ_215867,RMVar_hsa_circ_215868 4094 RMVar_ID_4094 Human_SNP_ID_122818351 A-to-I Human chr3 + 11417947 11417947 11417947 ATTCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCACCCACCACCATTCTTGGCTGATTTTT ATTCTGCCTCAGCCTCCCGAGTAGCTGGGACTGCAGGCACCCACCACCATTCTTGGCTGATTTTT A G ATG7 Ensembl:ENSG00000197548 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1316940560 Functional Loss SNV dbSNP153 33..33 33 - - - 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_8831,RMVar_hsa_circ_215904,RMVar_hsa_circ_318163,RMVar_hsa_circ_215903 4095 RMVar_ID_4095 Human_SNP_ID_122821957 A-to-I Human chr3 + 11431604 11431604 11431604 CCCTGGCAACCACTAATCTTCTTTCTGTCTGTAAGGATTTTTCTATTCTGGACACATCACATAAA CCCTGGCAACCACTAATCTTCTTTCTGTCTGTGAGGATTTTTCTATTCTGGACACATCACATAAA A G ATG7 Ensembl:ENSG00000197548 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs758760177 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108562,RMVar_hsa_circ_215894,RMVar_hsa_circ_215904 4096 RMVar_ID_4096 Human_SNP_ID_122824903 A-to-I Human chr3 + 11442647 11442647 11442647 TTAGGGCCAGGTGCGTGGGATTACATGCCTGTAATCTCAGCACTTTGGGAGTCTGAGGTGGGAGG TTAGGGCCAGGTGCGTGGGATTACATGCCTGTGATCTCAGCACTTTGGGAGTCTGAGGTGGGAGG A G ATG7 Ensembl:ENSG00000197548 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 29129909,30559470 RNA-Seq:(High) rs941833697 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108562,RMVar_hsa_circ_215894,RMVar_hsa_circ_215904 4097 RMVar_ID_4097 Human_SNP_ID_122825024 A-to-I Human chr3 + 11442846 11442846 11442846 GGGAGGCTGAGATGGGAAGATTGCTAGAGCCCAGGAGTTCGAGGCTGCATTGAGCTAAGATTGTG GGGAGGCTGAGATGGGAAGATTGCTAGAGCCCGGGAGTTCGAGGCTGCATTGAGCTAAGATTGTG A G ATG7 Ensembl:ENSG00000197548 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1035322143 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108562,RMVar_hsa_circ_215894,RMVar_hsa_circ_215904 4098 RMVar_ID_4098 Human_SNP_ID_122827194 A-to-I Human chr3 + 11451311 11451311 11451311 TTGGCTCACTGAAACCTCGGCCTCCTGGGTACAAGTGATTCTCATGCCTCAGCCTCCTGAGTAGC TTGGCTCACTGAAACCTCGGCCTCCTGGGTACTAGTGATTCTCATGCCTCAGCCTCCTGAGTAGC A T ATG7 Ensembl:ENSG00000197548 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1156958248 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108562,RMVar_hsa_circ_215894,RMVar_hsa_circ_215904 4099 RMVar_ID_4099 Human_SNP_ID_122827575 A-to-I Human chr3 + 11452348 11452348 11452348 TGGAGGTTGCAGTGAGCCATGATCACGCCACTACACCCCAGTCTGGGCGACAGAGCGAGAACCTG TGGAGGTTGCAGTGAGCCATGATCACGCCACTGCACCCCAGTCTGGGCGACAGAGCGAGAACCTG A G ATG7 Ensembl:ENSG00000197548 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1196500893 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108562,RMVar_hsa_circ_215894,RMVar_hsa_circ_215904 4100 RMVar_ID_4100 Human_SNP_ID_122831431 A-to-I Human chr3 + 11467003 11467003 11467003 ACAAAAAATTAGGTGTGGTGGCGGGCGCCTGTAATCTCAGCTGCTTTGGAGGCTGAGGCAGGAGA ACAAAAAATTAGGTGTGGTGGCGGGCGCCTGTGATCTCAGCTGCTTTGGAGGCTGAGGCAGGAGA A G ATG7 Ensembl:ENSG00000197548 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1259844198 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108562,RMVar_hsa_circ_215894,RMVar_hsa_circ_215904 4101 RMVar_ID_4101 Human_SNP_ID_122846056 A-to-I Human chr3 + 11516936 11516936 11516936 GAAACCCCGTCTGTACTAAAAATCCACAAATTAGCCGGGTATGGTGGCACGTGCCTGTAGTCCCA GAAACCCCGTCTGTACTAAAAATCCACAAATTGGCCGGGTATGGTGGCACGTGCCTGTAGTCCCA A G ATG7 Ensembl:ENSG00000197548 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1269777362 Functional Loss SNV dbSNP153 33..33 33 - - - 4102 RMVar_ID_4102 Human_SNP_ID_122846414 A-to-I Human chr3 + 11518370 11518370 11518370 GAGATCGAGACCAGCTTGGCCAACAATGGTGAAACCCTGTCTCTACTAAAAATACAAAAATTAGC GAGATCGAGACCAGCTTGGCCAACAATGGTGACACCCTGTCTCTACTAAAAATACAAAAATTAGC A C ATG7 Ensembl:ENSG00000197548 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1418185393 Functional Loss SNV dbSNP153 33..33 33 - - - 4103 RMVar_ID_4103 Human_SNP_ID_122887441 A-to-I Human chr3 - 11669758 11669758 11669758 GGAGGATTTCTTGGGACCAGGAGGTCGAGGCTATAATGAGCTGTGATCACACCATTGTTCTCCAG GGAGGATTTCTTGGGACCAGGAGGTCGAGGCTGTAATGAGCTGTGATCACACCATTGTTCTCCAG T C VGLL4 Ensembl:ENSG00000144560 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934278694 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_215908,RMVar_hsa_circ_93656,RMVar_hsa_circ_215906,RMVar_hsa_circ_273847 4104 RMVar_ID_4104 Human_SNP_ID_122919786 A-to-I Human chr3 - 11794257 11794257 11794257 TGGCATGTACCTGTAGCCCCAGCTACTCAGGAAGATGAGGAGAGAGGATCTCTTGAGCCCAGAAG TGGCATGTACCTGTAGCCCCAGCTACTCAGGAGGATGAGGAGAGAGGATCTCTTGAGCCCAGAAG T C TAMM41 Ensembl:ENSG00000144559 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1396487903 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7107106,Human_RBP_ID_14575417 RMVar_hsa_circ_79069,RMVar_hsa_circ_215911 4105 RMVar_ID_4105 Human_SNP_ID_122922321 A-to-I Human chr3 - 11805166 11805166 11805166 GAAACCCCGTCTCTACTAAAATACAAAAAATTAGCTGGGCGTGGTGGCACATGCCTGTAGTCCCA GAAACCCCGTCTCTACTAAAATACAAAAAATTCGCTGGGCGTGGTGGCACATGCCTGTAGTCCCA T G TAMM41 Ensembl:ENSG00000144559 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1159067840 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79069,RMVar_hsa_circ_215911 4106 RMVar_ID_4106 Human_SNP_ID_122923817 A-to-I Human chr3 - 11810842 11810842 11810842 TAGGGCTGATGTTGAATTTTTGTGCTCAAGCAATTCTCCTGCCTCAGCCTCCCAAACTGTTGGGA TAGGGCTGATGTTGAATTTTTGTGCTCAAGCAGTTCTCCTGCCTCAGCCTCCCAAACTGTTGGGA T C TAMM41 Ensembl:ENSG00000144559 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1471169150 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_395211,Human_Splice_Rec_395216,Human_Splice_Rec_395217 RMVar_hsa_circ_79069,RMVar_hsa_circ_101250,RMVar_hsa_circ_215911,RMVar_hsa_circ_215913,RMVar_hsa_circ_317927,RMVar_hsa_circ_325874,RMVar_hsa_circ_300767,RMVar_hsa_circ_30734,RMVar_hsa_circ_215914,RMVar_hsa_circ_215916,RMVar_hsa_circ_215917,RMVar_hsa_circ_215915,RMVar_hsa_circ_306029,RMVar_hsa_circ_367509,RMVar_hsa_circ_332309,RMVar_hsa_circ_277664,RMVar_hsa_circ_215920,RMVar_hsa_circ_215921,RMVar_hsa_circ_215922 4107 RMVar_ID_4107 Human_SNP_ID_122929581 A-to-I Human chr3 - 11834149 11834149 11834149 TACTCGACCTCCCGGGCTCAACCAATCCTCCCATCTCAGCCTCCTGAGTAGCCGGAACTATAGGC TACTCGACCTCCCGGGCTCAACCAATCCTCCCGTCTCAGCCTCCTGAGTAGCCGGAACTATAGGC T C TAMM41 Ensembl:ENSG00000144559 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1407486747 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79069,RMVar_hsa_circ_101250,RMVar_hsa_circ_215911,RMVar_hsa_circ_215913,RMVar_hsa_circ_325874,RMVar_hsa_circ_30734,RMVar_hsa_circ_215914,RMVar_hsa_circ_332309,RMVar_hsa_circ_215923,RMVar_hsa_circ_215922,RMVar_hsa_circ_215924,RMVar_hsa_circ_377173,RMVar_hsa_circ_305384,RMVar_hsa_circ_215927,RMVar_hsa_circ_215928,RMVar_hsa_circ_371334,RMVar_hsa_circ_215930 4108 RMVar_ID_4108 Human_SNP_ID_123017406 A-to-I Human chr3 - 12184789 12184789 12184789 GTGCCCGTTCCCAGCCTGGCCGGGAGATGGCAAGATGAGGCACTGAAGCTGAGGCCTGGTTTAAT GTGCCCGTTCCCAGCCTGGCCGGGAGATGGCATGATGAGGCACTGAAGCTGAGGCCTGGTTTAAT T A - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs540180858 Functional Loss SNV dbSNP153 33..33 33 - - - 4109 RMVar_ID_4109 Human_SNP_ID_123099522 A-to-I Human chr3 + 12523565 12523563 12523566 TTTTTTTTTTTTTTTTTTTGAGACAAAGTCTCACTTTGTTGCCTTGGCTGGAGTGCAGTGGCACG TTTTTTTTTTTTTTTTTTTGAGACAAAGTCT___TTTGTTGCCTTGGCTGGAGTGCAGTGGCACG TCAC T TSEN2 Ensembl:ENSG00000154743 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1362747693 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_332260,RMVar_hsa_circ_358610,RMVar_hsa_circ_58418,RMVar_hsa_circ_215956,RMVar_hsa_circ_349702,RMVar_hsa_circ_18387,RMVar_hsa_circ_45287,RMVar_hsa_circ_309578,RMVar_hsa_circ_307167,RMVar_hsa_circ_268141,RMVar_hsa_circ_42251,RMVar_hsa_circ_215969,RMVar_hsa_circ_215970,RMVar_hsa_circ_291528 4110 RMVar_ID_4110 Human_SNP_ID_123099551 A-to-I Human chr3 + 12523633 12523633 12523633 TCGATCTCGGCTCACTACAACCTCTGCCTCCCAGGTTCAAACCATTCTCCTGCCTCAGCTTCCCA TCGATCTCGGCTCACTACAACCTCTGCCTCCCGGGTTCAAACCATTCTCCTGCCTCAGCTTCCCA A G TSEN2 Ensembl:ENSG00000154743 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1354495209 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_332260,RMVar_hsa_circ_358610,RMVar_hsa_circ_58418,RMVar_hsa_circ_215956,RMVar_hsa_circ_349702,RMVar_hsa_circ_18387,RMVar_hsa_circ_45287,RMVar_hsa_circ_309578,RMVar_hsa_circ_307167,RMVar_hsa_circ_268141,RMVar_hsa_circ_42251,RMVar_hsa_circ_215969,RMVar_hsa_circ_215970,RMVar_hsa_circ_291528 4111 RMVar_ID_4111 Human_SNP_ID_123100068 A-to-I Human chr3 + 12525593 12525593 12525593 TTTATGTAGTTTTTGAGACAAGGTCTCACTCTATCCCCGAGGGTGGAGTGCAGTGGCACAATCTC TTTATGTAGTTTTTGAGACAAGGTCTCACTCTGTCCCCGAGGGTGGAGTGCAGTGGCACAATCTC A G TSEN2 Ensembl:ENSG00000154743 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs572319290 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_332260,RMVar_hsa_circ_358610,RMVar_hsa_circ_58418,RMVar_hsa_circ_215956,RMVar_hsa_circ_349702,RMVar_hsa_circ_18387,RMVar_hsa_circ_45287,RMVar_hsa_circ_309578,RMVar_hsa_circ_307167,RMVar_hsa_circ_268141,RMVar_hsa_circ_42251,RMVar_hsa_circ_215969,RMVar_hsa_circ_215970,RMVar_hsa_circ_291528 4112 RMVar_ID_4112 Human_SNP_ID_123103234 A-to-I Human chr3 + 12537265 12537265 12537265 CAAATAATTTTAAAAAATTAGCTGGGTGTGGTAGCATGCATCTGTAGTCCCAGCCACTGGGAAGG CAAATAATTTTAAAAAATTAGCTGGGTGTGGTGGCATGCATCTGTAGTCCCAGCCACTGGGAAGG A G TSEN2 Ensembl:ENSG00000154743 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs776887349 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85095,RMVar_hsa_circ_215973,RMVar_hsa_circ_215974 4113 RMVar_ID_4113 Human_SNP_ID_123103694 A-to-I Human chr3 + 12539189 12539189 12539189 GTAGTCTCGCTCTGTCGTCCAGGCTGGAGTCCAATGCTGCGATCTTGGATCACTGCAACCTCTGC GTAGTCTCGCTCTGTCGTCCAGGCTGGAGTCCGATGCTGCGATCTTGGATCACTGCAACCTCTGC A G TSEN2 Ensembl:ENSG00000154743 Protein coding exon GSE38233 cultured B-cells - 24183664 RNA-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 4114 RMVar_ID_4114 Human_SNP_ID_123103722 A-to-I Human chr3 + 12539244 12539244 12539244 CAACCTCTGCCTGCTGGGTTTAAGCGATTCTCATGCCTCAGCCTCCTGAGTAGCTGGGATTACAG CAACCTCTGCCTGCTGGGTTTAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAG A C TSEN2 Ensembl:ENSG00000154743 Protein coding exon GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1471566934 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25694060 Human_Splice_Rec_395778,Human_Splice_Rec_395808 RMVar_hsa_circ_85095,RMVar_hsa_circ_215973,RMVar_hsa_circ_215974 4115 RMVar_ID_4115 Human_SNP_ID_123103723 A-to-I Human chr3 + 12539244 12539244 12539244 CAACCTCTGCCTGCTGGGTTTAAGCGATTCTCATGCCTCAGCCTCCTGAGTAGCTGGGATTACAG CAACCTCTGCCTGCTGGGTTTAAGCGATTCTCGTGCCTCAGCCTCCTGAGTAGCTGGGATTACAG A G TSEN2 Ensembl:ENSG00000154743 Protein coding exon GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1471566934 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25694060 Human_Splice_Rec_395778,Human_Splice_Rec_395808 RMVar_hsa_circ_85095,RMVar_hsa_circ_215973,RMVar_hsa_circ_215974 4116 RMVar_ID_4116 Human_SNP_ID_123103761 A-to-I Human chr3 + 12539314 12539312 12539314 CACCACCACACACGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACTATGTTGGCCAGGC CACCACCACACACGGCTAATTTTTGTATTTT__GTAGAGACGGGGTTTCACTATGTTGGCCAGGC TTA T TSEN2 Ensembl:ENSG00000154743 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs796955979 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_85095,RMVar_hsa_circ_215973,RMVar_hsa_circ_215974 4117 RMVar_ID_4117 Human_SNP_ID_123103762 A-to-I Human chr3 + 12539314 12539314 12539314 CACCACCACACACGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACTATGTTGGCCAGGC CACCACCACACACGGCTAATTTTTGTATTTTTGGTAGAGACGGGGTTTCACTATGTTGGCCAGGC A G TSEN2 Ensembl:ENSG00000154743 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1301279070 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85095,RMVar_hsa_circ_215973,RMVar_hsa_circ_215974 4118 RMVar_ID_4118 Human_SNP_ID_123105847 A-to-I Human chr3 + 12545838 12545838 12545838 ACTCTTATTTATTTATTTAGAGACAGGGTCTCACTCTGTCACCCAAGCTAGAGTGCAGTGGCACG ACTCTTATTTATTTATTTAGAGACAGGGTCTCTCTCTGTCACCCAAGCTAGAGTGCAGTGGCACG A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1014718631 Functional Loss SNV dbSNP153 33..33 33 - - - 4119 RMVar_ID_4119 Human_SNP_ID_123105880 A-to-I Human chr3 + 12545968 12545968 12545968 AGCTGGGACTACAGACACACGCCACTATACCCAACTAATTGTTGTGTTTTTTGGTAGAGATGGGG AGCTGGGACTACAGACACACGCCACTATACCCCACTAATTGTTGTGTTTTTTGGTAGAGATGGGG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879091934 Functional Loss SNV dbSNP153 33..33 33 - - - 4120 RMVar_ID_4120 Human_SNP_ID_123106162 A-to-I Human chr3 + 12546965 12546965 12546965 TGGGGTGTACAATTTAAAAATAATTTTTAGCTAGGTGTGCTGGTGCACGCCTGTAGTCCCAGTTA TGGGGTGTACAATTTAAAAATAATTTTTAGCTCGGTGTGCTGGTGCACGCCTGTAGTCCCAGTTA A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1020315204 Functional Loss SNV dbSNP153 33..33 33 - - - 4121 RMVar_ID_4121 Human_SNP_ID_123106931 A-to-I Human chr3 + 12549647 12549647 12549647 AGTGCTCATTGCAGCCTCAAACTTCTGGGCTCAAGGGATCCTCCCACTTCAGCCTCCCAATCAGC AGTGCTCATTGCAGCCTCAAACTTCTGGGCTCCAGGGATCCTCCCACTTCAGCCTCCCAATCAGC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917130485 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8557447 4122 RMVar_ID_4122 Human_SNP_ID_123106945 A-to-I Human chr3 + 12549734 12549734 12549734 CACAGCTGGCTAATATTTTAATTTTAATTTTTATAGAGACAGGGTCTTGTTATGTTGCCCAGGCT CACAGCTGGCTAATATTTTAATTTTAATTTTTGTAGAGACAGGGTCTTGTTATGTTGCCCAGGCT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444063575 Functional Loss SNV dbSNP153 33..33 33 - - - 4123 RMVar_ID_4123 Human_SNP_ID_123112859 A-to-I Human chr3 + 12572683 12572683 12572683 TCGGCTCACTGCAACCTCTGCTTCCCTGGCTCAGGTGATCCTCCTGCCTCAGCCCCACCGAGTAG TCGGCTCACTGCAACCTCTGCTTCCCTGGCTCGGGTGATCCTCCTGCCTCAGCCCCACCGAGTAG A G MKRN2 Ensembl:ENSG00000075975 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1014207841 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2360,RMVar_hsa_circ_23460,RMVar_hsa_circ_100505,RMVar_hsa_circ_215978,RMVar_hsa_circ_16324,RMVar_hsa_circ_215980,RMVar_hsa_circ_326722 4124 RMVar_ID_4124 Human_SNP_ID_123119582 A-to-I Human chr3 - 12595303 12595302 12595303 CTTTAGGAGGCTGAGGTGGGAGAATCACTTGAAGTCAGGAATTTGAGACCAGCCTGGGCAACATG CTTTAGGAGGCTGAGGTGGGAGAATCACTTGA_GTCAGGAATTTGAGACCAGCCTGGGCAACATG CT C RAF1 Ensembl:ENSG00000132155 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs887749101 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_14332,RMVar_hsa_circ_84407,RMVar_hsa_circ_215987,RMVar_hsa_circ_310115,RMVar_hsa_circ_43270,RMVar_hsa_circ_125826,RMVar_hsa_circ_33183,RMVar_hsa_circ_215989 4125 RMVar_ID_4125 Human_SNP_ID_123120210 A-to-I Human chr3 - 12597667 12597667 12597667 CAAGCGATCCGCCTGCCTCGGCCTCCCAAAGTACTGGGATTGCAGGTGTGAGCCACTGTGCTCAG CAAGCGATCCGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTGCAGGTGTGAGCCACTGTGCTCAG T C RAF1 Ensembl:ENSG00000132155 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1362174708 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25694421 RMVar_hsa_circ_14332,RMVar_hsa_circ_84407,RMVar_hsa_circ_215987,RMVar_hsa_circ_310115,RMVar_hsa_circ_43270,RMVar_hsa_circ_125826,RMVar_hsa_circ_33183,RMVar_hsa_circ_215989 4126 RMVar_ID_4126 Human_SNP_ID_123120435 A-to-I Human chr3 - 12598560 12598560 12598560 CCAGCTAATTTGTTTTACCTTTTGTAGAGACAAGGTCTCACTATGTTGCCCAGGCTGGTCTCCAA CCAGCTAATTTGTTTTACCTTTTGTAGAGACAGGGTCTCACTATGTTGCCCAGGCTGGTCTCCAA T C RAF1 Ensembl:ENSG00000132155 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1448897566 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14332,RMVar_hsa_circ_84407,RMVar_hsa_circ_215987,RMVar_hsa_circ_310115,RMVar_hsa_circ_43270,RMVar_hsa_circ_125826,RMVar_hsa_circ_33183,RMVar_hsa_circ_215989 4127 RMVar_ID_4127 Human_SNP_ID_123122941 A-to-I Human chr3 - 12607829 12607829 12607829 CTCCTGCCTCAGCCTCCCGAGTAGCTCAGACTACAGGCACACACCACCACGCCCAGCTAATTTTT CTCCTGCCTCAGCCTCCCGAGTAGCTCAGACTGCAGGCACACACCACCACGCCCAGCTAATTTTT T C RAF1 Ensembl:ENSG00000132155 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1004464049 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14332,RMVar_hsa_circ_84407,RMVar_hsa_circ_215987,RMVar_hsa_circ_43270,RMVar_hsa_circ_118584,RMVar_hsa_circ_349801,RMVar_hsa_circ_323691,RMVar_hsa_circ_52302,RMVar_hsa_circ_215991,RMVar_hsa_circ_215994,RMVar_hsa_circ_292156,RMVar_hsa_circ_48816,RMVar_hsa_circ_215995,RMVar_hsa_circ_312920,RMVar_hsa_circ_319111,RMVar_hsa_circ_349215,RMVar_hsa_circ_291632,RMVar_hsa_circ_215998,RMVar_hsa_circ_215999,RMVar_hsa_circ_335225,RMVar_hsa_circ_289431,RMVar_hsa_circ_216000,RMVar_hsa_circ_216001 4128 RMVar_ID_4128 Human_SNP_ID_123125162 A-to-I Human chr3 - 12615970 12615970 12615970 TCGGCTCACTGCAACCTCTACCTCCCAGGTTCAAGCGATTCTCCTTGCCTCAGCCTCCCAAGTAG TCGGCTCACTGCAACCTCTACCTCCCAGGTTCGAGCGATTCTCCTTGCCTCAGCCTCCCAAGTAG T C RAF1 Ensembl:ENSG00000132155 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1247594588 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14332,RMVar_hsa_circ_349801,RMVar_hsa_circ_312920,RMVar_hsa_circ_215999,RMVar_hsa_circ_335225,RMVar_hsa_circ_216000,RMVar_hsa_circ_306103,RMVar_hsa_circ_22762 4129 RMVar_ID_4129 Human_SNP_ID_123125480 A-to-I Human chr3 - 12617219 12617219 12617219 AATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCACTCGAACCCGGGAGGCAGAGGTTGCAGT AATCCCAGCTACTTGGGAGGCTGAGGCAGGAGGATCACTCGAACCCGGGAGGCAGAGGTTGCAGT T C RAF1 Ensembl:ENSG00000132155 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs916176845 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14332,RMVar_hsa_circ_349801,RMVar_hsa_circ_312920,RMVar_hsa_circ_215999,RMVar_hsa_circ_335225,RMVar_hsa_circ_216000,RMVar_hsa_circ_306103,RMVar_hsa_circ_22762 4130 RMVar_ID_4130 Human_SNP_ID_123132723 A-to-I Human chr3 - 12642750 12642750 12642750 CACCCCCTGGCCCTGCCCCAATAGCTGGGACTACAGGCCCATGCCACCATACGCAGCTATTTTGT CACCCCCTGGCCCTGCCCCAATAGCTGGGACTTCAGGCCCATGCCACCATACGCAGCTATTTTGT T A RAF1 Ensembl:ENSG00000132155 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946835092 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1616968 4131 RMVar_ID_4131 Human_SNP_ID_123132724 A-to-I Human chr3 - 12642750 12642750 12642750 CACCCCCTGGCCCTGCCCCAATAGCTGGGACTACAGGCCCATGCCACCATACGCAGCTATTTTGT CACCCCCTGGCCCTGCCCCAATAGCTGGGACTGCAGGCCCATGCCACCATACGCAGCTATTTTGT T C RAF1 Ensembl:ENSG00000132155 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946835092 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1616968 4132 RMVar_ID_4132 Human_SNP_ID_123160198 A-to-I Human chr3 - 12739961 12739961 12739961 GTGAGAGCCAGACATGGTGGCTCACACCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAAGA GTGAGAGCCAGACATGGTGGCTCACACCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAAGA T C TMEM40 Ensembl:ENSG00000088726 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs983781017 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98460,RMVar_hsa_circ_114418,RMVar_hsa_circ_216005,RMVar_hsa_circ_216007,RMVar_hsa_circ_216008,RMVar_hsa_circ_122587 4133 RMVar_ID_4133 Human_SNP_ID_123312099 A-to-I Human chr3 - 13316340 13316339 13316340 GCCATGTGGTTGATTTTTCTAAAGCTGGAGAAAGGAAGAATTGTGCCTTGCATATTACTTGAGCT GCCATGTGGTTGATTTTTCTAAAGCTGGAGAA_GGAAGAATTGTGCCTTGCATATTACTTGAGCT CT C NUP210 Ensembl:ENSG00000132182 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1350488050 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_589937,Human_RBP_ID_3686887,Human_RBP_ID_5120203,Human_RBP_ID_7123188,Human_RBP_ID_24382626 4134 RMVar_ID_4134 Human_SNP_ID_123325817 A-to-I Human chr3 - 13367313 13367313 13367313 CTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGACAGGCGCCACCACACGCGGCTAATTCTG CTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTGCAGACAGGCGCCACCACACGCGGCTAATTCTG T C NUP210 Ensembl:ENSG00000132182 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1458104400 Functional Loss SNV dbSNP153 33..33 33 - - - 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 4135 RMVar_ID_4135 Human_SNP_ID_123329297 A-to-I Human chr3 - 13380481 13380481 13380481 TGCGCAATGGTGAGCAGGCTGCTCATCTTGATATCCTCAGTCCCCTATCCCCAAAATGTGGCTCT TGCGCAATGGTGAGCAGGCTGCTCATCTTGATGTCCTCAGTCCCCTATCCCCAAAATGTGGCTCT T C NUP210 Ensembl:ENSG00000132182 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4684933 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_114,GWAS_ID_115,GWAS_ID_116,GWAS_ID_117 RMVar_hsa_circ_122264,RMVar_hsa_circ_216042,RMVar_hsa_circ_89460,RMVar_hsa_circ_216043,RMVar_hsa_circ_4353,RMVar_hsa_circ_97575,RMVar_hsa_circ_216046,RMVar_hsa_circ_8821,RMVar_hsa_circ_84954,RMVar_hsa_circ_120406,RMVar_hsa_circ_367268,RMVar_hsa_circ_377406,RMVar_hsa_circ_38044,RMVar_hsa_circ_216055,RMVar_hsa_circ_216054,RMVar_hsa_circ_346081 4136 RMVar_ID_4136 Human_SNP_ID_123329453 A-to-I Human chr3 - 13381183 13381183 13381183 AGTATAAAGTAATGTTGCTTCATTGAGCAACTATGTTATTTTATTCTGACATTTATCTTTGATGC AGTATAAAGTAATGTTGCTTCATTGAGCAACTGTGTTATTTTATTCTGACATTTATCTTTGATGC T C NUP210 Ensembl:ENSG00000132182 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11707261 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_118,GWAS_ID_119,GWAS_ID_120,GWAS_ID_121 RMVar_hsa_circ_122264,RMVar_hsa_circ_216042,RMVar_hsa_circ_89460,RMVar_hsa_circ_216043,RMVar_hsa_circ_4353,RMVar_hsa_circ_97575,RMVar_hsa_circ_216046,RMVar_hsa_circ_8821,RMVar_hsa_circ_84954,RMVar_hsa_circ_120406,RMVar_hsa_circ_367268,RMVar_hsa_circ_377406,RMVar_hsa_circ_38044,RMVar_hsa_circ_216055,RMVar_hsa_circ_216054,RMVar_hsa_circ_346081 4137 RMVar_ID_4137 Human_SNP_ID_123329939 A-to-I Human chr3 - 13383068 13383068 13383068 ATGATCATGGCTCACAGCAGCTTTGACCTCCCAGGCTCAAGTGATCCTCTCACCTCACACCCCTG ATGATCATGGCTCACAGCAGCTTTGACCTCCCGGGCTCAAGTGATCCTCTCACCTCACACCCCTG T C NUP210 Ensembl:ENSG00000132182 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs562593302 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122264,RMVar_hsa_circ_216042,RMVar_hsa_circ_89460,RMVar_hsa_circ_216043,RMVar_hsa_circ_4353,RMVar_hsa_circ_97575,RMVar_hsa_circ_216046,RMVar_hsa_circ_8821,RMVar_hsa_circ_84954,RMVar_hsa_circ_120406,RMVar_hsa_circ_367268,RMVar_hsa_circ_377406,RMVar_hsa_circ_38044,RMVar_hsa_circ_216055,RMVar_hsa_circ_216054,RMVar_hsa_circ_346081 4138 RMVar_ID_4138 Human_SNP_ID_123336216 A-to-I Human chr3 - 13407798 13407798 13407798 ATATCACTAATAGCCCAGTATTTATGGTTTCAATAAGTGGATGAATGCCTTAAAGACCTCAAGGA ATATCACTAATAGCCCAGTATTTATGGTTTCATTAAGTGGATGAATGCCTTAAAGACCTCAAGGA T A NUP210 Ensembl:ENSG00000132182 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4684936 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8559343 GWAS_ID_122,GWAS_ID_123,GWAS_ID_124,GWAS_ID_125,GWAS_ID_126,GWAS_ID_127,GWAS_ID_128,GWAS_ID_129,GWAS_ID_130,GWAS_ID_131,GWAS_ID_132,GWAS_ID_133,GWAS_ID_134,GWAS_ID_135,GWAS_ID_136,GWAS_ID_137,GWAS_ID_138,GWAS_ID_139,GWAS_ID_140,GWAS_ID_141,GWAS_ID_142,GWAS_ID_143,GWAS_ID_144,GWAS_ID_145,GWAS_ID_146,GWAS_ID_147,GWAS_ID_148,GWAS_ID_149 RMVar_hsa_circ_89460,RMVar_hsa_circ_216043,RMVar_hsa_circ_84954,RMVar_hsa_circ_216054 4139 RMVar_ID_4139 Human_SNP_ID_123336217 A-to-I Human chr3 - 13407798 13407798 13407798 ATATCACTAATAGCCCAGTATTTATGGTTTCAATAAGTGGATGAATGCCTTAAAGACCTCAAGGA ATATCACTAATAGCCCAGTATTTATGGTTTCAGTAAGTGGATGAATGCCTTAAAGACCTCAAGGA T C NUP210 Ensembl:ENSG00000132182 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4684936 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8559343 GWAS_ID_122,GWAS_ID_123,GWAS_ID_124,GWAS_ID_125,GWAS_ID_126,GWAS_ID_127,GWAS_ID_128,GWAS_ID_129,GWAS_ID_130,GWAS_ID_131,GWAS_ID_132,GWAS_ID_133,GWAS_ID_134,GWAS_ID_135,GWAS_ID_136,GWAS_ID_137,GWAS_ID_138,GWAS_ID_139,GWAS_ID_140,GWAS_ID_141,GWAS_ID_142,GWAS_ID_143,GWAS_ID_144,GWAS_ID_145,GWAS_ID_146,GWAS_ID_147,GWAS_ID_148,GWAS_ID_149 RMVar_hsa_circ_89460,RMVar_hsa_circ_216043,RMVar_hsa_circ_84954,RMVar_hsa_circ_216054 4140 RMVar_ID_4140 Human_SNP_ID_123337156 A-to-I Human chr3 - 13411213 13411213 13411213 ACTTTTATTTTTCTGAGACAGATTCTTGCTCTATCACCCAGGCTGCAGTGCAGTGGCACAATTAT ACTTTTATTTTTCTGAGACAGATTCTTGCTCTGTCACCCAGGCTGCAGTGCAGTGGCACAATTAT T C NUP210 Ensembl:ENSG00000132182 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs113595848 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89460,RMVar_hsa_circ_216043,RMVar_hsa_circ_84954,RMVar_hsa_circ_216054 4141 RMVar_ID_4141 Human_SNP_ID_123338423 A-to-I Human chr3 - 13415962 13415962 13415962 TGAGGGGTGACTGTGGGAGGCCAGAGGCCAGCACTACCCTTGCGTGTGGATGTCCTGGGTCCCTC TGAGGGGTGACTGTGGGAGGCCAGAGGCCAGCGCTACCCTTGCGTGTGGATGTCCTGGGTCCCTC T C NUP210 Ensembl:ENSG00000132182 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs9842462 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_150,GWAS_ID_151,GWAS_ID_152,GWAS_ID_153,GWAS_ID_154,GWAS_ID_155,GWAS_ID_156,GWAS_ID_157,GWAS_ID_158,GWAS_ID_159,GWAS_ID_160,GWAS_ID_161,GWAS_ID_162,GWAS_ID_163,GWAS_ID_164,GWAS_ID_165,GWAS_ID_166,GWAS_ID_167,GWAS_ID_168,GWAS_ID_169,GWAS_ID_170,GWAS_ID_171,GWAS_ID_172,GWAS_ID_173,GWAS_ID_174,GWAS_ID_175,GWAS_ID_176,GWAS_ID_177 RMVar_hsa_circ_89460,RMVar_hsa_circ_216043,RMVar_hsa_circ_84954,RMVar_hsa_circ_216054 4142 RMVar_ID_4142 Human_SNP_ID_123338424 A-to-I Human chr3 - 13415962 13415962 13415962 TGAGGGGTGACTGTGGGAGGCCAGAGGCCAGCACTACCCTTGCGTGTGGATGTCCTGGGTCCCTC TGAGGGGTGACTGTGGGAGGCCAGAGGCCAGCCCTACCCTTGCGTGTGGATGTCCTGGGTCCCTC T G NUP210 Ensembl:ENSG00000132182 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs9842462 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_150,GWAS_ID_151,GWAS_ID_152,GWAS_ID_153,GWAS_ID_154,GWAS_ID_155,GWAS_ID_156,GWAS_ID_157,GWAS_ID_158,GWAS_ID_159,GWAS_ID_160,GWAS_ID_161,GWAS_ID_162,GWAS_ID_163,GWAS_ID_164,GWAS_ID_165,GWAS_ID_166,GWAS_ID_167,GWAS_ID_168,GWAS_ID_169,GWAS_ID_170,GWAS_ID_171,GWAS_ID_172,GWAS_ID_173,GWAS_ID_174,GWAS_ID_175,GWAS_ID_176,GWAS_ID_177 RMVar_hsa_circ_89460,RMVar_hsa_circ_216043,RMVar_hsa_circ_84954,RMVar_hsa_circ_216054 4143 RMVar_ID_4143 Human_SNP_ID_123345749 A-to-I Human chr3 - 13444796 13444796 13444796 CTCGCACTCTGTCACTCAGGCTGGAGTTCAGTAGCACGATCTCGGCTCACTGCAACCTCTGCCTC CTCGCACTCTGTCACTCAGGCTGGAGTTCAGTGGCACGATCTCGGCTCACTGCAACCTCTGCCTC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1447830284 Functional Loss SNV dbSNP153 33..33 33 - - - 4144 RMVar_ID_4144 Human_SNP_ID_123347638 A-to-I Human chr3 - 13450951 13450951 13450951 GGGTTCAAGCAATTCCCCTGCCTCAGCCTCCCAAGAAGCTGGGATAACCATATGCCACCGCGCCC GGGTTCAAGCAATTCCCCTGCCTCAGCCTCCCTAGAAGCTGGGATAACCATATGCCACCGCGCCC T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1428815212 Functional Loss SNV dbSNP153 33..33 33 - - - 4145 RMVar_ID_4145 Human_SNP_ID_123533704 A-to-I Human chr3 - 14172985 14172985 14172985 AAGTTTCACAAGGAAAGAGGAAAAGAGGCTGCAGTCATCCTGGGGGTTCAGCAGATGGTCCAGCA AAGTTTCACAAGGAAAGAGGAAAAGAGGCTGCGGTCATCCTGGGGGTTCAGCAGATGGTCCAGCA T C XPC Ensembl:ENSG00000154767 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1126482 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_934846,Human_RBP_ID_1633058,Human_RBP_ID_5530213,Human_RBP_ID_7130824,Human_RBP_ID_9393337,Human_RBP_ID_19009884,Human_RBP_ID_26347771,Human_RBP_ID_27821938 Human_Splice_Rec_397210,Human_Splice_Rec_397240,Human_Splice_Rec_397296 RMVar_hsa_circ_60924,RMVar_hsa_circ_364754,RMVar_hsa_circ_336902 4146 RMVar_ID_4146 Human_SNP_ID_123596040 A-to-I Human chr3 + 14416875 14416875 14416875 AAAGGTTTGTTTTTGTTTTGAGACAGGGTCACACTCTGTCGCCTACGCTGGGGTGCAGTGGTGTC AAAGGTTTGTTTTTGTTTTGAGACAGGGTCACCCTCTGTCGCCTACGCTGGGGTGCAGTGGTGTC A C SLC6A6 Ensembl:ENSG00000131389 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1289858037 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100719,RMVar_hsa_circ_216070 4147 RMVar_ID_4147 Human_SNP_ID_123596041 A-to-I Human chr3 + 14416875 14416875 14416875 AAAGGTTTGTTTTTGTTTTGAGACAGGGTCACACTCTGTCGCCTACGCTGGGGTGCAGTGGTGTC AAAGGTTTGTTTTTGTTTTGAGACAGGGTCACGCTCTGTCGCCTACGCTGGGGTGCAGTGGTGTC A G SLC6A6 Ensembl:ENSG00000131389 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1289858037 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100719,RMVar_hsa_circ_216070 4148 RMVar_ID_4148 Human_SNP_ID_123729029 A-to-I Human chr3 - 14944597 14944597 14944597 GTGATCCTCCCATCTTGGCCTCCCAAAGTGTTAGGATTACAGGCGTGAGCCACCACACCCTGCCT GTGATCCTCCCATCTTGGCCTCCCAAAGTGTTGGGATTACAGGCGTGAGCCACCACACCCTGCCT T C FGD5-AS1 Ensembl:ENSG00000225733 lincRNA intron GSE38233;GSE100210;GSE112787 cultured B-cells;HepG2 cell line;293 Flip-In T-REx cells,empty vector - 24183664,29129909,29967493 RNA-Seq:(High) rs1127505 Functional Loss SNV dbSNP153 33..33 33 - - - 4149 RMVar_ID_4149 Human_SNP_ID_123729040 A-to-I Human chr3 - 14944630 14944630 14944630 TTGACCAGGCTGGTCTCGAACTCCTGGCCTCAAGTGATCCTCCCATCTTGGCCTCCCAAAGTGTT TTGACCAGGCTGGTCTCGAACTCCTGGCCTCAGGTGATCCTCCCATCTTGGCCTCCCAAAGTGTT T C FGD5-AS1 Ensembl:ENSG00000225733 lincRNA intron GSE38233;GSE100210;GSE112787;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;293 Flip-In T-REx cells,empty vector;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,29967493,31158229,31158229,32596459,32596459 RNA-Seq:(High) rs1407314766 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_248726 4150 RMVar_ID_4150 Human_SNP_ID_123729147 A-to-I Human chr3 - 14944928 14944928 14944928 TGGCTCATGCCTGTAATCCCAGCATTTTGGGAAGGTGAGGTGGGTGGATCACCTGAGGTCAGGAG TGGCTCATGCCTGTAATCCCAGCATTTTGGGAGGGTGAGGTGGGTGGATCACCTGAGGTCAGGAG T C FGD5-AS1 Ensembl:ENSG00000225733 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-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 4151 RMVar_ID_4151 Human_SNP_ID_123729150 A-to-I Human chr3 - 14944940 14944940 14944940 GGCCGGGCATGGTGGCTCATGCCTGTAATCCCAGCATTTTGGGAAGGTGAGGTGGGTGGATCACC GGCCGGGCATGGTGGCTCATGCCTGTAATCCCGGCATTTTGGGAAGGTGAGGTGGGTGGATCACC T C FGD5-AS1 Ensembl:ENSG00000225733 lincRNA intron GSE38233;GSE112787 cultured B-cells;293 Flip-In T-REx cells,empty vector - 24183664,29967493 RNA-Seq:(High) rs1138884 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4726914,Human_RBP_ID_5089837,Human_RBP_ID_5654819,Human_RBP_ID_26510848,Human_RBP_ID_27047191,Human_RBP_ID_27314433 RMVar_hsa_circ_216093,RMVar_hsa_circ_112835 4152 RMVar_ID_4152 Human_SNP_ID_123729161 A-to-I Human chr3 - 14944964 14944964 14944964 TTTGTTTTTTTAATAGATGGCATTGGCCGGGCATGGTGGCTCATGCCTGTAATCCCAGCATTTTG TTTGTTTTTTTAATAGATGGCATTGGCCGGGCGTGGTGGCTCATGCCTGTAATCCCAGCATTTTG T C FGD5-AS1 Ensembl:ENSG00000225733 lincRNA intron GSE38233;GSE100210;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,temporal_cortex - 24183664,29129909,30559470 RNA-Seq:(High) rs577099499 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_592375,Human_RBP_ID_1633220,Human_RBP_ID_4759146,Human_RBP_ID_5089837,Human_RBP_ID_5654819,Human_RBP_ID_8211217,Human_RBP_ID_24496178,Human_RBP_ID_26510848,Human_RBP_ID_27047191 RMVar_hsa_circ_216093,RMVar_hsa_circ_112835 4153 RMVar_ID_4153 Human_SNP_ID_123742548 A-to-I Human chr3 + 14993292 14993292 14993292 CCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCCGGGCATGGTGGTGG CCTGGCCAACATGGTGAAACCCCGTCTCTACTGAAAATACAAAAATTAGCCGGGCATGGTGGTGG A G NR2C2 Ensembl:ENSG00000177463 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1380119468 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49950 4154 RMVar_ID_4154 Human_SNP_ID_452817378 A-to-I Human chr11 - 128382 128382 128382 AACAGGCCACCGTGAGGGAGGAACAGGATCGCACTCGGGCTGCTGGGAGGTAGGCAGGGACTTGG AACAGGCCACCGTGAGGGAGGAACAGGATCGCTCTCGGGCTGCTGGGAGGTAGGCAGGGACTTGG T A LINC01001 Ensembl:ENSG00000230724 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1394196514 Functional Loss SNV dbSNP153 33..33 33 - - - 4155 RMVar_ID_4155 Human_SNP_ID_452817643 A-to-I Human chr11 - 129063 129063 129063 GCTCTTGCCCCCACGGCGGCCTCTCGGGGCCAAGTCCCTGCCTGCCTCCCAGCAGCCCGCGTGCG GCTCTTGCCCCCACGGCGGCCTCTCGGGGCCACGTCCCTGCCTGCCTCCCAGCAGCCCGCGTGCG T G LINC01001 Ensembl:ENSG00000230724 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1222610724 Functional Loss SNV dbSNP153 33..33 33 - - - 4156 RMVar_ID_4156 Human_SNP_ID_452918822 A-to-I Human chr11 - 449256 449256 449256 CGAGACCAGCCTAGGCAAAGTGGTGACACCCCATCTTTACTAAAAATACAAAAATTGCCCTGGCA CGAGACCAGCCTAGGCAAAGTGGTGACACCCCCTCTTTACTAAAAATACAAAAATTGCCCTGGCA T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1393147889 Functional Loss SNV dbSNP153 33..33 33 - - - 4157 RMVar_ID_4157 Human_SNP_ID_452923005 A-to-I Human chr11 + 463231 463231 463231 CTAGAAATTAGGCTTAATTTTATTTTTTATTTATTTTATTTTTTTTTGAGATGGAGTCTCGCTCT CTAGAAATTAGGCTTAATTTTATTTTTTATTTTTTTTATTTTTTTTTGAGATGGAGTCTCGCTCT A T PTDSS2 Ensembl:ENSG00000174915 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1463933714 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6075527 RMVar_hsa_circ_88435,RMVar_hsa_circ_315236,RMVar_hsa_circ_309355,RMVar_hsa_circ_147399,RMVar_hsa_circ_147400 4158 RMVar_ID_4158 Human_SNP_ID_452923066 A-to-I Human chr11 + 463388 463388 463388 TAGCTGGGAATACAGGGCCCACCACCATGCCCAGACAGTTTTTGTATTTTTAGTGGAGACGGGGT TAGCTGGGAATACAGGGCCCACCACCATGCCCGGACAGTTTTTGTATTTTTAGTGGAGACGGGGT A G PTDSS2 Ensembl:ENSG00000174915 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444197570 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 4159 RMVar_ID_4159 Human_SNP_ID_452938919 A-to-I Human chr11 + 508349 508349 508349 ACGCCTGGCTAATTGTTGTATTTTATGTAGAGAAGAGGTCTCCCTGTGTTGCCCAGCCTGGTCTT ACGCCTGGCTAATTGTTGTATTTTATGTAGAGGAGAGGTCTCCCTGTGTTGCCCAGCCTGGTCTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs905582917 Functional Loss SNV dbSNP153 33..33 33 - - - 4160 RMVar_ID_4160 Human_SNP_ID_452939398 A-to-I Human chr11 + 509770 509770 509770 TAATTTTAATAGAGACAGGGTTTCAGCGTGTTAGCCAGGATGGTCTCGAGCTCCTGACCTTGTGA TAATTTTAATAGAGACAGGGTTTCAGCGTGTTGGCCAGGATGGTCTCGAGCTCCTGACCTTGTGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005892671 Functional Loss SNV dbSNP153 33..33 33 - - - 4161 RMVar_ID_4161 Human_SNP_ID_452940279 A-to-I Human chr11 + 512216 512216 512216 TGCCTGCCCTGGCCTCCCAAAGTGCTGGGATTATAGGTGTGAGCCACAAAGCCTTTTTGTTTTCA TGCCTGCCCTGGCCTCCCAAAGTGCTGGGATTGTAGGTGTGAGCCACAAAGCCTTTTTGTTTTCA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs763137967 Functional Loss SNV dbSNP153 33..33 33 - - - 4162 RMVar_ID_4162 Human_SNP_ID_452940310 A-to-I Human chr11 + 512305 512305 512305 TCGCCCAGGCTGGAGTGCAGTGGCATGATCTCAGCTCACTGCAACCTCTGCATCCCAGTTCAAGC TCGCCCAGGCTGGAGTGCAGTGGCATGATCTCGGCTCACTGCAACCTCTGCATCCCAGTTCAAGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1303881236 Functional Loss SNV dbSNP153 33..33 33 - - - 4163 RMVar_ID_4163 Human_SNP_ID_452940319 A-to-I Human chr11 + 512338 512338 512338 GCTCACTGCAACCTCTGCATCCCAGTTCAAGCAGTTCTCCGCCTCGGCCTCCTGAGTAGCTGGGA GCTCACTGCAACCTCTGCATCCCAGTTCAAGCGGTTCTCCGCCTCGGCCTCCTGAGTAGCTGGGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs557582388 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11641768 4164 RMVar_ID_4164 Human_SNP_ID_452940627 A-to-I Human chr11 + 513352 513352 513352 TTTTTGTATTGTATTAGAGACAGGGTTTCACCATGTTGGCGAGGCTGGTCCCGAACTCCTGGCCT TTTTTGTATTGTATTAGAGACAGGGTTTCACCGTGTTGGCGAGGCTGGTCCCGAACTCCTGGCCT A G AC137894.3 Ensembl:ENSG00000288033 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1036572255 Functional Loss SNV dbSNP153 33..33 33 - - - 4165 RMVar_ID_4165 Human_SNP_ID_452967020 A-to-I Human chr11 + 582334 582334 582334 TTGCCCAGGCTGGAGTACAGTGGTGCCATCTCAGCTCACTGCAACTTCTGCCTCCCGGGTTCAAG TTGCCCAGGCTGGAGTACAGTGGTGCCATCTCGGCTCACTGCAACTTCTGCCTCCCGGGTTCAAG A G PHRF1 Ensembl:ENSG00000070047 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1004343654 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18825,RMVar_hsa_circ_123643,RMVar_hsa_circ_147423,RMVar_hsa_circ_318600,RMVar_hsa_circ_147421,RMVar_hsa_circ_349239,RMVar_hsa_circ_68954 4166 RMVar_ID_4166 Human_SNP_ID_452967397 A-to-I Human chr11 + 583208 583208 583208 TAAAAATAGAAAAATTAGCCAGTCGTGTTGGCACGCGCCTGTAATCCCAGCTACTTGGGAGGCTG TAAAAATAGAAAAATTAGCCAGTCGTGTTGGCGCGCGCCTGTAATCCCAGCTACTTGGGAGGCTG A G PHRF1 Ensembl:ENSG00000070047 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1171801230 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18825,RMVar_hsa_circ_123643,RMVar_hsa_circ_147423,RMVar_hsa_circ_318600,RMVar_hsa_circ_147421,RMVar_hsa_circ_349239,RMVar_hsa_circ_68954 4167 RMVar_ID_4167 Human_SNP_ID_452968413 A-to-I Human chr11 + 585936 585936 585936 CAGGCTGGAGTGCAATCGTGCAGTCTAGGCTCACTGCAACCTCTGCTTCCCAGGTTCAAGCGATT CAGGCTGGAGTGCAATCGTGCAGTCTAGGCTCCCTGCAACCTCTGCTTCCCAGGTTCAAGCGATT A C PHRF1 Ensembl:ENSG00000070047 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1257583125 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11647904 RMVar_hsa_circ_18825,RMVar_hsa_circ_123643,RMVar_hsa_circ_147423,RMVar_hsa_circ_318600,RMVar_hsa_circ_147421,RMVar_hsa_circ_349239,RMVar_hsa_circ_68954 4168 RMVar_ID_4168 Human_SNP_ID_452969497 A-to-I Human chr11 + 589015 589015 589015 AAAATTATCCGGGCGTGGTACCACGTACCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTATCCGGGCGTGGTACCACGTACCTGTGGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA A G PHRF1 Ensembl:ENSG00000070047 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs765755393 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18825,RMVar_hsa_circ_123643,RMVar_hsa_circ_147421,RMVar_hsa_circ_349239,RMVar_hsa_circ_68954,RMVar_hsa_circ_9181,RMVar_hsa_circ_352573,RMVar_hsa_circ_377204,RMVar_hsa_circ_292143,RMVar_hsa_circ_14890,RMVar_hsa_circ_147424 4169 RMVar_ID_4169 Human_SNP_ID_452973324 A-to-I Human chr11 + 599350 599350 599350 TTGGCTCACTGCATCCTCCACCTTCCGGGTTCAAGTGTTTCTCCTGCCTCAGCCTCCCAAGTAGC TTGGCTCACTGCATCCTCCACCTTCCGGGTTCGAGTGTTTCTCCTGCCTCAGCCTCCCAAGTAGC A G PHRF1 Ensembl:ENSG00000070047 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1187043653 Functional Loss SNV dbSNP153 33..33 33 - - - 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 4170 RMVar_ID_4170 Human_SNP_ID_452974377 A-to-I Human chr11 + 602494 602486 602495 CCTGAGGTCAGGAGTTCAAGGCCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAAGAC CCTGAGGTCAGGAGTTCAAGGCCAG_________CATGGTGAAACCCCATCTCTACTAAAAAGAC GCCTGGCCAA G PHRF1 Ensembl:ENSG00000070047 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1422032879 Functional Loss DEL dbSNP153 26..34 33 - - - RMVar_hsa_circ_123643,RMVar_hsa_circ_147421,RMVar_hsa_circ_269055,RMVar_hsa_circ_96813,RMVar_hsa_circ_147425 4171 RMVar_ID_4171 Human_SNP_ID_452974379 A-to-I Human chr11 + 602497 602497 602497 GAGGTCAGGAGTTCAAGGCCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAAGACTAA GAGGTCAGGAGTTCAAGGCCAGCCTGGCCAACGTGGTGAAACCCCATCTCTACTAAAAAGACTAA A G PHRF1 Ensembl:ENSG00000070047 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs140802650 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123643,RMVar_hsa_circ_147421,RMVar_hsa_circ_269055,RMVar_hsa_circ_96813,RMVar_hsa_circ_147425 4172 RMVar_ID_4172 Human_SNP_ID_452974380 A-to-I Human chr11 + 602497 602497 602497 GAGGTCAGGAGTTCAAGGCCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAAGACTAA GAGGTCAGGAGTTCAAGGCCAGCCTGGCCAACTTGGTGAAACCCCATCTCTACTAAAAAGACTAA A T PHRF1 Ensembl:ENSG00000070047 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs140802650 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123643,RMVar_hsa_circ_147421,RMVar_hsa_circ_269055,RMVar_hsa_circ_96813,RMVar_hsa_circ_147425 4173 RMVar_ID_4173 Human_SNP_ID_452984215 A-to-I Human chr11 + 622513 622513 622513 CAGTCTCGCTCTGTCGTCACCCAGGCTGGAGTACAGTGGTGTGATCTCGGCTCACTGCAACCTCT CAGTCTCGCTCTGTCGTCACCCAGGCTGGAGTGCAGTGGTGTGATCTCGGCTCACTGCAACCTCT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1476589182 Functional Loss SNV dbSNP153 33..33 33 - - - 4174 RMVar_ID_4174 Human_SNP_ID_452988260 A-to-I Human chr11 + 632144 632144 632144 CTCCCACCTCAGATTCCCAAAAAGCTGTGACTATAGGCTCACGCCACCACACCCAGCTAATGTTT CTCCCACCTCAGATTCCCAAAAAGCTGTGACTGTAGGCTCACGCCACCACACCCAGCTAATGTTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025272702 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11661690 4175 RMVar_ID_4175 Human_SNP_ID_452988654 A-to-I Human chr11 + 633441 633441 633441 CCCAGCTGTTCAGGAGGCTGAGGCAGGAGAATAGCGTGAACCCGGGAGGCAGAGGTTGTGGTGAG CCCAGCTGTTCAGGAGGCTGAGGCAGGAGAATGGCGTGAACCCGGGAGGCAGAGGTTGTGGTGAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285989090 Functional Loss SNV dbSNP153 33..33 33 - - - 4176 RMVar_ID_4176 Human_SNP_ID_452988874 A-to-I Human chr11 + 633896 633896 633896 TCACTGCAAGCTCTGCCTCCCGGGTTCACGCCATTCCCTTGCCTCAGCCTCCCGAGTAGCTGGGA TCACTGCAAGCTCTGCCTCCCGGGTTCACGCCGTTCCCTTGCCTCAGCCTCCCGAGTAGCTGGGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1002711094 Functional Loss SNV dbSNP153 33..33 33 - - - 4177 RMVar_ID_4177 Human_SNP_ID_452994547 A-to-I Human chr11 - 645041 645041 645041 CTCCTGCCTCAGCTTCCCGAGTAGCTGGGATTAGAGGTGCCTGCCACCATGCCCAGCTAATTTTT CTCCTGCCTCAGCTTCCCGAGTAGCTGGGATTCGAGGTGCCTGCCACCATGCCCAGCTAATTTTT T G DEAF1 Ensembl:ENSG00000177030 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1287849775 Functional Loss SNV dbSNP153 33..33 33 - - - 4178 RMVar_ID_4178 Human_SNP_ID_452994748 A-to-I Human chr11 - 645597 645597 645597 AAACAGAACTGGGGCGGGGCGCAGTGGCTCACACCTGTCATCCCAGCACTTTGGGAGGCCGAGGC AAACAGAACTGGGGCGGGGCGCAGTGGCTCACGCCTGTCATCCCAGCACTTTGGGAGGCCGAGGC T C DEAF1 Ensembl:ENSG00000177030 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968320824 Functional Loss SNV dbSNP153 33..33 33 - - - 4179 RMVar_ID_4179 Human_SNP_ID_452994896 A-to-I Human chr11 - 646036 646036 646036 GTTGGGCAGGCTGGTCTCGAGCTCCTGGCCTCAGGTGATCTGCCCACCTCGGCCTCCCAACATGA GTTGGGCAGGCTGGTCTCGAGCTCCTGGCCTCGGGTGATCTGCCCACCTCGGCCTCCCAACATGA T C DEAF1 Ensembl:ENSG00000177030 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1380984280 Functional Loss SNV dbSNP153 33..33 33 - - - 4180 RMVar_ID_4180 Human_SNP_ID_452996001 A-to-I Human chr11 - 649310 649310 649310 TCAAGCAATACTCCTCCTTCAGCCTCCCAAGTAACTGGGATTACAGGCACCCGCCACCATGCCCG TCAAGCAATACTCCTCCTTCAGCCTCCCAAGTTACTGGGATTACAGGCACCCGCCACCATGCCCG T A DEAF1 Ensembl:ENSG00000177030 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs181292551 Functional Loss SNV dbSNP153 33..33 33 - - - 4181 RMVar_ID_4181 Human_SNP_ID_452996016 A-to-I Human chr11 - 649365 649365 649365 CAGGCCAGAGTGCAGTGGCACAATCTCAGCTCAGTGCAACCTCCGCTTCCCGGGTTCAAGCAATA CAGGCCAGAGTGCAGTGGCACAATCTCAGCTCGGTGCAACCTCCGCTTCCCGGGTTCAAGCAATA T C DEAF1 Ensembl:ENSG00000177030 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1425712283 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11759915 4182 RMVar_ID_4182 Human_SNP_ID_452996174 A-to-I Human chr11 - 649834 649834 649834 TTTAGTAGAGATGGGGTTTCTCCGTGTTGGCAAGGCTGGTCTCGAACTCCTGACCTCAGGTGATC TTTAGTAGAGATGGGGTTTCTCCGTGTTGGCAGGGCTGGTCTCGAACTCCTGACCTCAGGTGATC T C DEAF1 Ensembl:ENSG00000177030 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1298723705 Functional Loss SNV dbSNP153 33..33 33 - - - 4183 RMVar_ID_4183 Human_SNP_ID_452996204 A-to-I Human chr11 - 649969 649969 649969 CAGGCTGGAGTGCAATGGCACGATCTCAGCCCACTGCAACCTCAACGTCCCGGGTTCAAGTGATT CAGGCTGGAGTGCAATGGCACGATCTCAGCCCCCTGCAACCTCAACGTCCCGGGTTCAAGTGATT T G DEAF1 Ensembl:ENSG00000177030 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs970987011 Functional Loss SNV dbSNP153 33..33 33 - - - 4184 RMVar_ID_4184 Human_SNP_ID_452996219 A-to-I Human chr11 - 650011 650007 650011 TTTGTTTTTGTTTTTGTTTTTTAGACAATCTCACTCTGTCGCCAGGCTGGAGTGCAATGGCACGA TTTGTTTTTGTTTTTGTTTTTTAGACAATCTC____TGTCGCCAGGCTGGAGTGCAATGGCACGA AGAGT A DEAF1 Ensembl:ENSG00000177030 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs942722562 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_6084918,Human_RBP_ID_11669680 4185 RMVar_ID_4185 Human_SNP_ID_452996221 A-to-I Human chr11 - 650016 650016 650016 TTGTTTTTGTTTTTGTTTTTGTTTTTTAGACAATCTCACTCTGTCGCCAGGCTGGAGTGCAATGG TTGTTTTTGTTTTTGTTTTTGTTTTTTAGACAGTCTCACTCTGTCGCCAGGCTGGAGTGCAATGG T C DEAF1 Ensembl:ENSG00000177030 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1314407414 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1162733,Human_RBP_ID_6084918,Human_RBP_ID_11669680 4186 RMVar_ID_4186 Human_SNP_ID_452996419 A-to-I Human chr11 - 650624 650624 650624 AAAAACCTTTTTGGCTGGGTGCAGTGGCCCACACCAGTCATCCCAACACTTTGGGAGGCCAAGAG AAAAACCTTTTTGGCTGGGTGCAGTGGCCCACGCCAGTCATCCCAACACTTTGGGAGGCCAAGAG T C DEAF1 Ensembl:ENSG00000177030 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984405168 Functional Loss SNV dbSNP153 33..33 33 - - - 4187 RMVar_ID_4187 Human_SNP_ID_452996474 A-to-I Human chr11 - 650791 650791 650791 CGCCCCACGCCCAGCTAATTCTTTGTATTTTTAGTTGAGACGGGGTTTCGCCATTTTGCCCAGGC CGCCCCACGCCCAGCTAATTCTTTGTATTTTTTGTTGAGACGGGGTTTCGCCATTTTGCCCAGGC T A DEAF1 Ensembl:ENSG00000177030 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005438686 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11670675 4188 RMVar_ID_4188 Human_SNP_ID_452996476 A-to-I Human chr11 - 650806 650805 650806 GCCTCTACAGATACACGCCCCACGCCCAGCTAATTCTTTGTATTTTTAGTTGAGACGGGGTTTCG GCCTCTACAGATACACGCCCCACGCCCAGCTA_TTCTTTGTATTTTTAGTTGAGACGGGGTTTCG AT A DEAF1 Ensembl:ENSG00000177030 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1564922782 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_6085067 4189 RMVar_ID_4189 Human_SNP_ID_452996542 A-to-I Human chr11 - 651036 651036 651036 ATTGCTTGAACCTGGGAGGCGGAGGTTGCAGTAAGCCAAGATCACTCCACTGCACTCTAGTCTGG ATTGCTTGAACCTGGGAGGCGGAGGTTGCAGTGAGCCAAGATCACTCCACTGCACTCTAGTCTGG T C DEAF1 Ensembl:ENSG00000177030 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs145623560 Functional Loss SNV dbSNP153 33..33 33 - - - 4190 RMVar_ID_4190 Human_SNP_ID_452996570 A-to-I Human chr11 - 651142 651142 651142 CTTGGCTAACATGGTAAGACCCCATCTCTACTAAAAACACAAAAATTAGCCAGGCGTGGTGGCGC CTTGGCTAACATGGTAAGACCCCATCTCTACTGAAAACACAAAAATTAGCCAGGCGTGGTGGCGC T C DEAF1 Ensembl:ENSG00000177030 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1403175785 Functional Loss SNV dbSNP153 33..33 33 - - - 4191 RMVar_ID_4191 Human_SNP_ID_452996777 A-to-I Human chr11 - 651834 651834 651834 TCGCCCAGGCTGGAGTGTAGTGGCGCCATCTCAGCTCACCGCAAGCTCCGCCTCCCAGGTTCACG TCGCCCAGGCTGGAGTGTAGTGGCGCCATCTCGGCTCACCGCAAGCTCCGCCTCCCAGGTTCACG T C DEAF1 Ensembl:ENSG00000177030 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs934587053 Functional Loss SNV dbSNP153 33..33 33 - - - 4192 RMVar_ID_4192 Human_SNP_ID_452996994 A-to-I Human chr11 - 652630 652630 652630 TCTGCCCTCCTTCTCTATTTTCTTTTTGAGACAGTTTTGCTCTGTAGCCCAGGCTGGAGTGCAGT TCTGCCCTCCTTCTCTATTTTCTTTTTGAGACGGTTTTGCTCTGTAGCCCAGGCTGGAGTGCAGT T C DEAF1 Ensembl:ENSG00000177030 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1050367207 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1781436,Human_RBP_ID_11673499 4193 RMVar_ID_4193 Human_SNP_ID_452997080 A-to-I Human chr11 - 652918 652918 652918 CACCATACCTGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTCTCACCACGTTGGGCAAGCTGG CACCATACCTGGCTAATTTTTGTATTTTTAGTGGAGACGGGGTCTCACCACGTTGGGCAAGCTGG T C DEAF1 Ensembl:ENSG00000177030 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1460963718 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11674140 4194 RMVar_ID_4194 Human_SNP_ID_452998318 A-to-I Human chr11 - 656129 656129 656129 AAAGTTTGTCATTTAAAGTAGAGGCACAGGCCAGGCGCGGTGGCTCATGCCTGTAATCCCAGCAC AAAGTTTGTCATTTAAAGTAGAGGCACAGGCCGGGCGCGGTGGCTCATGCCTGTAATCCCAGCAC T C DEAF1 Ensembl:ENSG00000177030 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1287672062 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25398,RMVar_hsa_circ_88751,RMVar_hsa_circ_98127,RMVar_hsa_circ_73638,RMVar_hsa_circ_147430,RMVar_hsa_circ_147431 4195 RMVar_ID_4195 Human_SNP_ID_453001894 A-to-I Human chr11 - 668784 668784 668784 AGGGTTTCACTTTGTCACCCAGGCTGGAGTACAGAGGTGTGACCTCGGCTCACTGCAGCCTCAAG AGGGTTTCACTTTGTCACCCAGGCTGGAGTACTGAGGTGTGACCTCGGCTCACTGCAGCCTCAAG T A DEAF1 Ensembl:ENSG00000177030 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs951755038 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22471519 RMVar_hsa_circ_25398,RMVar_hsa_circ_88751,RMVar_hsa_circ_98127,RMVar_hsa_circ_73638,RMVar_hsa_circ_147430,RMVar_hsa_circ_147431 4196 RMVar_ID_4196 Human_SNP_ID_453002465 A-to-I Human chr11 - 670532 670526 670533 TTTTGGTATTTTAGGAGAGAAGAGGTTTCGCCATGTTGGCGAGGCTGGTCTTAAACTCCAGGCCT TTTTGGTATTTTAGGAGAGAAGAGGTTTCGC_______GCGAGGCTGGTCTTAAACTCCAGGCCT CCAACATG C DEAF1 Ensembl:ENSG00000177030 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404728761 Functional Loss DEL dbSNP153 32..38 33 - - - Human_RBP_ID_23154950 RMVar_hsa_circ_25398,RMVar_hsa_circ_88751,RMVar_hsa_circ_98127,RMVar_hsa_circ_73638,RMVar_hsa_circ_147430,RMVar_hsa_circ_147431 4197 RMVar_ID_4197 Human_SNP_ID_453002505 A-to-I Human chr11 - 670684 670684 670684 TTTTGAGATGGTCTTGCTGTGTCACCCAGGCTAGAGTGCAGTGGTGTGATCTCGGCTCACTGCAG TTTTGAGATGGTCTTGCTGTGTCACCCAGGCTGGAGTGCAGTGGTGTGATCTCGGCTCACTGCAG T C DEAF1 Ensembl:ENSG00000177030 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025330031 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25398,RMVar_hsa_circ_88751,RMVar_hsa_circ_98127,RMVar_hsa_circ_73638,RMVar_hsa_circ_147430,RMVar_hsa_circ_147431 4198 RMVar_ID_4198 Human_SNP_ID_453002639 A-to-I Human chr11 - 670870 670870 670870 AAGAGGCTGAAACGTGAGGATTGCTTGAGCCTAGGAGGTTGATGTTGCAGTGAGCCGTGATCACA AAGAGGCTGAAACGTGAGGATTGCTTGAGCCTGGGAGGTTGATGTTGCAGTGAGCCGTGATCACA T C DEAF1 Ensembl:ENSG00000177030 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1341149133 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11687258 RMVar_hsa_circ_25398,RMVar_hsa_circ_88751,RMVar_hsa_circ_98127,RMVar_hsa_circ_73638,RMVar_hsa_circ_147430,RMVar_hsa_circ_147431 4199 RMVar_ID_4199 Human_SNP_ID_453002858 A-to-I Human chr11 - 671501 671501 671501 AAAATACTTTTTCACTGGGCACAGTGGATCACACTTGTAATCTCAGTGCTTTGAGAGGCTGAGGT AAAATACTTTTTCACTGGGCACAGTGGATCACGCTTGTAATCTCAGTGCTTTGAGAGGCTGAGGT T C DEAF1 Ensembl:ENSG00000177030 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903188349 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11687391 RMVar_hsa_circ_25398,RMVar_hsa_circ_88751,RMVar_hsa_circ_98127,RMVar_hsa_circ_73638,RMVar_hsa_circ_147430,RMVar_hsa_circ_147431 4200 RMVar_ID_4200 Human_SNP_ID_453018291 A-to-I Human chr11 + 718212 718212 718212 AAAATTAGTCGGGTGTGGTGGTGGGTGCCTATAATCCCACGTACTCGGGAAGCTGAAGCAGGAGT AAAATTAGTCGGGTGTGGTGGTGGGTGCCTATGATCCCACGTACTCGGGAAGCTGAAGCAGGAGT A G EPS8L2 Ensembl:ENSG00000177106 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1282226756 Functional Loss SNV dbSNP153 33..33 33 - - - 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 4201 RMVar_ID_4201 Human_SNP_ID_453031822 A-to-I Human chr11 + 757491 757491 757491 ATATTTGTATTTGTTTTTAGAGGCAGGGTTTCACCATGTTGCCCTAGCTGGTTTCGAACTCCTGA ATATTTGTATTTGTTTTTAGAGGCAGGGTTTCTCCATGTTGCCCTAGCTGGTTTCGAACTCCTGA A T TALDO1 Ensembl:ENSG00000177156 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1349156164 Functional Loss SNV dbSNP153 33..33 33 - - - 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 4202 RMVar_ID_4202 Human_SNP_ID_453031925 A-to-I Human chr11 + 757974 757973 757974 GTCTAGGCAATAGGGCAAAACTCTGTCTCTACAAAAAAATATAAAAATTAGCTGGGCATGGGCCA GTCTAGGCAATAGGGCAAAACTCTGTCTCTAC_AAAAAATATAAAAATTAGCTGGGCATGGGCCA CA C TALDO1 Ensembl:ENSG00000177156 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs35724844 Functional Loss DEL dbSNP153 33..33 33 - - - 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 4203 RMVar_ID_4203 Human_SNP_ID_453032822 A-to-I Human chr11 + 760846 760846 760846 CACGAGGTCAGGAGATCGAGACCATCCTGGCTAACACGGTGAAACCCCGACTCCACTAAAAAATA CACGAGGTCAGGAGATCGAGACCATCCTGGCTGACACGGTGAAACCCCGACTCCACTAAAAAATA A G TALDO1 Ensembl:ENSG00000177156 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1231663097 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116849,RMVar_hsa_circ_147450,RMVar_hsa_circ_114881,RMVar_hsa_circ_147449 4204 RMVar_ID_4204 Human_SNP_ID_453032875 A-to-I Human chr11 + 761072 761072 761072 AGAAAACTTTTAGGCCGGGCACGGTGGCTCATACCTGTAATCCTAGCACTCTGGAAGCCTGAGGT AGAAAACTTTTAGGCCGGGCACGGTGGCTCATTCCTGTAATCCTAGCACTCTGGAAGCCTGAGGT A T TALDO1 Ensembl:ENSG00000177156 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1232502665 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116849,RMVar_hsa_circ_147450 4205 RMVar_ID_4205 Human_SNP_ID_453032984 A-to-I Human chr11 - 761414 761414 761414 CTACTGGAACCTCAACTTCCCAGGCTCAAGCGATCCTCCCGCCTCAGCCTCCTAAGTAGCTGGAA CTACTGGAACCTCAACTTCCCAGGCTCAAGCGGTCCTCCCGCCTCAGCCTCCTAAGTAGCTGGAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934735869 Functional Loss SNV dbSNP153 33..33 33 - - - 4206 RMVar_ID_4206 Human_SNP_ID_453032993 A-to-I Human chr11 - 761444 761444 761444 CCAGGCTGGAGTGCAGTGGTACGATCATAGCTACTGGAACCTCAACTTCCCAGGCTCAAGCGATC CCAGGCTGGAGTGCAGTGGTACGATCATAGCTCCTGGAACCTCAACTTCCCAGGCTCAAGCGATC T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1039210028 Functional Loss SNV dbSNP153 33..33 33 - - - 4207 RMVar_ID_4207 Human_SNP_ID_453033126 A-to-I Human chr11 + 761912 761912 761912 GCTCAAGAGATCTCTACCCATCTTGGCCTCCCAAAGTGCTGGGATTATAGGCATGAGCCATTGTG GCTCAAGAGATCTCTACCCATCTTGGCCTCCCCAAGTGCTGGGATTATAGGCATGAGCCATTGTG A C TALDO1 Ensembl:ENSG00000177156 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs942283477 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116849,RMVar_hsa_circ_147450 4208 RMVar_ID_4208 Human_SNP_ID_453033173 A-to-I Human chr11 + 762030 762028 762030 CATTCTCGTCCATGCTGGAGTGCAATGGTGCTATCTCAGCTCACTGCAACCTCCACCTCTGGGGT CATTCTCGTCCATGCTGGAGTGCAATGGTGC__TCTCAGCTCACTGCAACCTCCACCTCTGGGGT CTA C TALDO1 Ensembl:ENSG00000177156 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1028539754 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_116849,RMVar_hsa_circ_147450 4209 RMVar_ID_4209 Human_SNP_ID_453033226 A-to-I Human chr11 + 762224 762224 762224 AGCCTCAGGTGATCCGCCCGCCTCGGCCTCCCAAAGTGTTGGGATCACAGGTTTGAGCCACTGCA AGCCTCAGGTGATCCGCCCGCCTCGGCCTCCCGAAGTGTTGGGATCACAGGTTTGAGCCACTGCA A G TALDO1 Ensembl:ENSG00000177156 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1384369834 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116849,RMVar_hsa_circ_147450 4210 RMVar_ID_4210 Human_SNP_ID_453033227 A-to-I Human chr11 + 762225 762225 762225 GCCTCAGGTGATCCGCCCGCCTCGGCCTCCCAAAGTGTTGGGATCACAGGTTTGAGCCACTGCAC GCCTCAGGTGATCCGCCCGCCTCGGCCTCCCATAGTGTTGGGATCACAGGTTTGAGCCACTGCAC A T TALDO1 Ensembl:ENSG00000177156 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1421210241 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116849,RMVar_hsa_circ_147450 4211 RMVar_ID_4211 Human_SNP_ID_453035514 A-to-I Human chr11 - 767854 767854 767854 AGAGCAAGACTCCATCTCAAAAAAAAAAAAAAAGAAAATATTGTAAACCTAGTGGCTTATAAACA AGAGCAAGACTCCATCTCAAAAAAAAAAAAAAGGAAAATATTGTAAACCTAGTGGCTTATAAACA T C GATD1 Ensembl:ENSG00000177225 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs111776686 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24918672 4212 RMVar_ID_4212 Human_SNP_ID_453035539 A-to-I Human chr11 - 767927 767927 767927 AGAATCGCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCTGACATCGTGCCACTGCACTCTAGTC AGAATCGCTTGAACCCAGGAGGCGGAGGTTGCGGTGAGCTGACATCGTGCCACTGCACTCTAGTC T C GATD1 Ensembl:ENSG00000177225 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1370461169 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5167661 4213 RMVar_ID_4213 Human_SNP_ID_453035556 A-to-I Human chr11 - 767988 767988 767988 AAATTAGCCGGGCGCGGTGGTGGGCGCCTGTAATCCCATTTACTTGGGAGGCTGAGGCAGGAGAA AAATTAGCCGGGCGCGGTGGTGGGCGCCTGTATTCCCATTTACTTGGGAGGCTGAGGCAGGAGAA T A GATD1 Ensembl:ENSG00000177225 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 29129909,30559470 RNA-Seq:(High) rs1253892427 Functional Loss SNV dbSNP153 33..33 33 - - - 4214 RMVar_ID_4214 Human_SNP_ID_453035557 A-to-I Human chr11 - 767988 767988 767988 AAATTAGCCGGGCGCGGTGGTGGGCGCCTGTAATCCCATTTACTTGGGAGGCTGAGGCAGGAGAA AAATTAGCCGGGCGCGGTGGTGGGCGCCTGTAGTCCCATTTACTTGGGAGGCTGAGGCAGGAGAA T C GATD1 Ensembl:ENSG00000177225 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 29129909,30559470 RNA-Seq:(High) rs1253892427 Functional Loss SNV dbSNP153 33..33 33 - - - 4215 RMVar_ID_4215 Human_SNP_ID_453035579 A-to-I Human chr11 - 768028 768028 768028 TGGCCAAGATGGTGAAACCCCGTCTCTACTAAAAATACAGAAATTAGCCGGGCGCGGTGGTGGGC TGGCCAAGATGGTGAAACCCCGTCTCTACTAAGAATACAGAAATTAGCCGGGCGCGGTGGTGGGC T C GATD1 Ensembl:ENSG00000177225 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1387732004 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11721366 4216 RMVar_ID_4216 Human_SNP_ID_453035581 A-to-I Human chr11 - 768033 768033 768033 CAGCCTGGCCAAGATGGTGAAACCCCGTCTCTACTAAAAATACAGAAATTAGCCGGGCGCGGTGG CAGCCTGGCCAAGATGGTGAAACCCCGTCTCTTCTAAAAATACAGAAATTAGCCGGGCGCGGTGG T A GATD1 Ensembl:ENSG00000177225 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1486135920 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11721366 4217 RMVar_ID_4217 Human_SNP_ID_453035608 A-to-I Human chr11 - 768123 768123 768123 AAACTGGCCGGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGTGGA AAACTGGCCGGGCACGGTGGCTCACGCCTGTAGTCCCAGCACTTTGGGAGGCTGAGGCAGGTGGA T C GATD1 Ensembl:ENSG00000177225 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs537183826 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23155074 4218 RMVar_ID_4218 Human_SNP_ID_453035749 A-to-I Human chr11 - 768509 768509 768509 AGCTAGGACTACAGGTGCACACCACCACACCCAGCTAATTTTTGTATTTTTCCTTTTTTTTTTTT AGCTAGGACTACAGGTGCACACCACCACACCCTGCTAATTTTTGTATTTTTCCTTTTTTTTTTTT T A GATD1 Ensembl:ENSG00000177225 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1329591610 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11721385 4219 RMVar_ID_4219 Human_SNP_ID_453035751 A-to-I Human chr11 - 768513 768513 768513 AAGTAGCTAGGACTACAGGTGCACACCACCACACCCAGCTAATTTTTGTATTTTTCCTTTTTTTT AAGTAGCTAGGACTACAGGTGCACACCACCACGCCCAGCTAATTTTTGTATTTTTCCTTTTTTTT T C GATD1 Ensembl:ENSG00000177225 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404016195 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11721385 4220 RMVar_ID_4220 Human_SNP_ID_453035759 A-to-I Human chr11 - 768537 768537 768537 GTGATTCTCCTGCCTCAGCCTCCCAAGTAGCTAGGACTACAGGTGCACACCACCACACCCAGCTA GTGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGTGCACACCACCACACCCAGCTA T C GATD1 Ensembl:ENSG00000177225 Protein coding intron GSE47997;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829 K562 cells&HepG2 cells;ASD brains,Fragile X samples from NIH NeuroBioBank;Bronchiolar epithelium,BEP2D cell line - 23474544,30559470,31158229 RNA-Seq:(High) rs1459547080 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24903576 4221 RMVar_ID_4221 Human_SNP_ID_453035768 A-to-I Human chr11 - 768571 768571 768571 TCGGCTCACTGCAGCCTCCGCCTCCCGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGC TCGGCTCACTGCAGCCTCCGCCTCCCGGGTTCGAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGC T C GATD1 Ensembl:ENSG00000177225 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs955097476 Functional Loss SNV dbSNP153 33..33 33 - - - 4222 RMVar_ID_4222 Human_SNP_ID_453035786 A-to-I Human chr11 - 768617 768617 768617 ATGGAGTCTCACTCTGTCGCCCAGGCTGGAACACAGTGGCACGATCTCGGCTCACTGCAGCCTCC ATGGAGTCTCACTCTGTCGCCCAGGCTGGAACGCAGTGGCACGATCTCGGCTCACTGCAGCCTCC T C GATD1 Ensembl:ENSG00000177225 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs925508877 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11721386,Human_RBP_ID_17560450,Human_RBP_ID_22471530,Human_RBP_ID_22709762,Human_RBP_ID_22896800,Human_RBP_ID_23155081,Human_RBP_ID_23305509,Human_RBP_ID_26410738,Human_RBP_ID_26897654 4223 RMVar_ID_4223 Human_SNP_ID_453035796 A-to-I Human chr11 - 768669 768669 768669 AGCCGCCACGTCCGGCTAACAAGTACTTTTTTATTTTTATTTTATTTTTTGGATGGAGTCTCACT AGCCGCCACGTCCGGCTAACAAGTACTTTTTTGTTTTTATTTTATTTTTTGGATGGAGTCTCACT T C GATD1 Ensembl:ENSG00000177225 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1477192839 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2285490,Human_RBP_ID_6096517,Human_RBP_ID_11721386,Human_RBP_ID_17801616,Human_RBP_ID_27619802 4224 RMVar_ID_4224 Human_SNP_ID_453035817 A-to-I Human chr11 - 768723 768723 768723 ACCTCAGGTGATCCATCTTCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCGCCACGT ACCTCAGGTGATCCATCTTCCTCAGCCTCCCAGAGTGCTGGGATTACAGGCGTGAGCCGCCACGT T C GATD1 Ensembl:ENSG00000177225 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs577904290 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24918674 4225 RMVar_ID_4225 Human_SNP_ID_453035840 A-to-I Human chr11 - 768816 768816 768816 GATTACAGGCGTGAGCCACTGCGCCCGGCGTAATTTTTGTTTTTAGTAGAGATGGGGTTTCATCA GATTACAGGCGTGAGCCACTGCGCCCGGCGTAGTTTTTGTTTTTAGTAGAGATGGGGTTTCATCA T C GATD1 Ensembl:ENSG00000177225 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs896486430 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11721400,Human_RBP_ID_23155085 4226 RMVar_ID_4226 Human_SNP_ID_453035859 A-to-I Human chr11 - 768850 768850 768850 GTGATCCTCCCGCCTCGGCCTCCCAAAGTGTTAGGATTACAGGCGTGAGCCACTGCGCCCGGCGT GTGATCCTCCCGCCTCGGCCTCCCAAAGTGTTTGGATTACAGGCGTGAGCCACTGCGCCCGGCGT T A GATD1 Ensembl:ENSG00000177225 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1007974930 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11721400 4227 RMVar_ID_4227 Human_SNP_ID_453035860 A-to-I Human chr11 - 768850 768850 768850 GTGATCCTCCCGCCTCGGCCTCCCAAAGTGTTAGGATTACAGGCGTGAGCCACTGCGCCCGGCGT GTGATCCTCCCGCCTCGGCCTCCCAAAGTGTTGGGATTACAGGCGTGAGCCACTGCGCCCGGCGT T C GATD1 Ensembl:ENSG00000177225 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1007974930 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11721400 4228 RMVar_ID_4228 Human_SNP_ID_453035930 A-to-I Human chr11 - 769018 769018 769018 TGGCTCACTGCAACCTCTGTCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCGGAGTAGCT TGGCTCACTGCAACCTCTGTCTCCCGGGTTCAGGCGATTCTCCTGCCTCAGCCTCCGGAGTAGCT T C GATD1 Ensembl:ENSG00000177225 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1052481813 Functional Loss SNV dbSNP153 33..33 33 - - - 4229 RMVar_ID_4229 Human_SNP_ID_453035949 A-to-I Human chr11 - 769054 769054 769054 TCTCGTCACCCAGGCTGGAGTGCAGTGGCACAATCTTGGCTCACTGCAACCTCTGTCTCCCGGGT TCTCGTCACCCAGGCTGGAGTGCAGTGGCACAGTCTTGGCTCACTGCAACCTCTGTCTCCCGGGT T C GATD1 Ensembl:ENSG00000177225 Protein coding intron GSE38233;GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,32596459 RNA-Seq:(High) rs1339292186 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23155088,Human_RBP_ID_24918676 4230 RMVar_ID_4230 Human_SNP_ID_453035950 A-to-I Human chr11 - 769055 769055 769055 CTCTCGTCACCCAGGCTGGAGTGCAGTGGCACAATCTTGGCTCACTGCAACCTCTGTCTCCCGGG CTCTCGTCACCCAGGCTGGAGTGCAGTGGCACTATCTTGGCTCACTGCAACCTCTGTCTCCCGGG T A GATD1 Ensembl:ENSG00000177225 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1478147234 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23155088,Human_RBP_ID_24918676 4231 RMVar_ID_4231 Human_SNP_ID_453035971 A-to-I Human chr11 - 769117 769117 769117 TGGTGATGGACCTCTGTGGACAAATGCTTTTTATTTTATTTATTTTTTGAGATGGAGTTTGTCTC TGGTGATGGACCTCTGTGGACAAATGCTTTTTTTTTTATTTATTTTTTGAGATGGAGTTTGTCTC T A GATD1 Ensembl:ENSG00000177225 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs202047001 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6096525 4232 RMVar_ID_4232 Human_SNP_ID_453036041 A-to-I Human chr11 - 769318 769315 769319 AACTCCGTCTCAAAAATAAAAAATAATAAAATAAAGCCGTTCAATAAGGAGAATTTGGAAAAAAG AACTCCGTCTCAAAAATAAAAAATAATAAAA____GCCGTTCAATAAGGAGAATTTGGAAAAAAG CTTTA C GATD1 Ensembl:ENSG00000177225 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1004471843 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_3380562,Human_RBP_ID_17801618,Human_RBP_ID_23155094,Human_RBP_ID_26606055,Human_RBP_ID_27416381 4233 RMVar_ID_4233 Human_SNP_ID_453036043 A-to-I Human chr11 - 769318 769318 769318 AACTCCGTCTCAAAAATAAAAAATAATAAAATAAAGCCGTTCAATAAGGAGAATTTGGAAAAAAG AACTCCGTCTCAAAAATAAAAAATAATAAAATTAAGCCGTTCAATAAGGAGAATTTGGAAAAAAG T A GATD1 Ensembl:ENSG00000177225 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs370065515 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3380562,Human_RBP_ID_17801618,Human_RBP_ID_23155094,Human_RBP_ID_26606055,Human_RBP_ID_27416381 4234 RMVar_ID_4234 Human_SNP_ID_453036068 A-to-I Human chr11 - 769388 769388 769388 TGAACCTGGGAGGCGGAAGTTGCAGTGAGCCAAGATTGCGCCATTGCACTCCAACCTGGGCAATG TGAACCTGGGAGGCGGAAGTTGCAGTGAGCCATGATTGCGCCATTGCACTCCAACCTGGGCAATG T A GATD1 Ensembl:ENSG00000177225 Protein coding intron GSE47997;GSE38233;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,29796672,31158229,32596459,32596459 RNA-Seq:(High) rs966877360 Functional Loss SNV dbSNP153 33..33 33 - - - 4235 RMVar_ID_4235 Human_SNP_ID_453036069 A-to-I Human chr11 - 769388 769388 769388 TGAACCTGGGAGGCGGAAGTTGCAGTGAGCCAAGATTGCGCCATTGCACTCCAACCTGGGCAATG TGAACCTGGGAGGCGGAAGTTGCAGTGAGCCAGGATTGCGCCATTGCACTCCAACCTGGGCAATG T C GATD1 Ensembl:ENSG00000177225 Protein coding intron GSE47997;GSE38233;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,29796672,31158229,32596459,32596459 RNA-Seq:(High) rs966877360 Functional Loss SNV dbSNP153 33..33 33 - - - 4236 RMVar_ID_4236 Human_SNP_ID_453036070 A-to-I Human chr11 - 769389 769389 769389 TTGAACCTGGGAGGCGGAAGTTGCAGTGAGCCAAGATTGCGCCATTGCACTCCAACCTGGGCAAT TTGAACCTGGGAGGCGGAAGTTGCAGTGAGCCCAGATTGCGCCATTGCACTCCAACCTGGGCAAT T G GATD1 Ensembl:ENSG00000177225 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs188882670 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24903597 4237 RMVar_ID_4237 Human_SNP_ID_453036071 A-to-I Human chr11 - 769397 769397 769397 AGAATTGCTTGAACCTGGGAGGCGGAAGTTGCAGTGAGCCAAGATTGCGCCATTGCACTCCAACC AGAATTGCTTGAACCTGGGAGGCGGAAGTTGCGGTGAGCCAAGATTGCGCCATTGCACTCCAACC T C GATD1 Ensembl:ENSG00000177225 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1041179025 Functional Loss SNV dbSNP153 33..33 33 - - - 4238 RMVar_ID_4238 Human_SNP_ID_453036074 A-to-I Human chr11 - 769403 769403 769403 GACGTGAGAATTGCTTGAACCTGGGAGGCGGAAGTTGCAGTGAGCCAAGATTGCGCCATTGCACT GACGTGAGAATTGCTTGAACCTGGGAGGCGGAGGTTGCAGTGAGCCAAGATTGCGCCATTGCACT T C GATD1 Ensembl:ENSG00000177225 Protein coding intron GSE47997;GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,29129909,31158229,31158229,31158229,32596459,32596459 RNA-Seq:(High) rs901335663 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11721428,Human_RBP_ID_18613200 4239 RMVar_ID_4239 Human_SNP_ID_453036075 A-to-I Human chr11 - 769403 769403 769403 GACGTGAGAATTGCTTGAACCTGGGAGGCGGAAGTTGCAGTGAGCCAAGATTGCGCCATTGCACT GACGTGAGAATTGCTTGAACCTGGGAGGCGGACGTTGCAGTGAGCCAAGATTGCGCCATTGCACT T G GATD1 Ensembl:ENSG00000177225 Protein coding intron GSE47997;GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,29129909,31158229,31158229,31158229,32596459,32596459 RNA-Seq:(High) rs901335663 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11721428,Human_RBP_ID_18613200 4240 RMVar_ID_4240 Human_SNP_ID_453036105 A-to-I Human chr11 - 769491 769491 769491 AAGCCTGGCCAACATGGTGAAACTAAAATACAAAAATGAGCCGGGTGTGGTGTCAGGCGCCTGTA AAGCCTGGCCAACATGGTGAAACTAAAATACAGAAATGAGCCGGGTGTGGTGTCAGGCGCCTGTA T C GATD1 Ensembl:ENSG00000177225 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1046197282 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_228014,Human_RBP_ID_11721434,Human_RBP_ID_17801619,Human_RBP_ID_22893995,Human_RBP_ID_23155097 Human_miRNA_ID_180660 4241 RMVar_ID_4241 Human_SNP_ID_453036120 A-to-I Human chr11 - 769533 769533 769533 AGGCCAAGGTGGGTGGATCATCTGAAGTCAGGAGTTTGGGAAAAGCCTGGCCAACATGGTGAAAC AGGCCAAGGTGGGTGGATCATCTGAAGTCAGGCGTTTGGGAAAAGCCTGGCCAACATGGTGAAAC T G GATD1 Ensembl:ENSG00000177225 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1487102284 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_32646,Human_RBP_ID_11721438,Human_RBP_ID_17560211,Human_RBP_ID_26408175 4242 RMVar_ID_4242 Human_SNP_ID_453036126 A-to-I Human chr11 - 769559 769559 769559 CACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGTGGATCATCTGAAGTCAGGAGTTTGG CACGCCTGTAATCCCAGCACTTTGGGAGGCCAGGGTGGGTGGATCATCTGAAGTCAGGAGTTTGG T C GATD1 Ensembl:ENSG00000177225 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1291991889 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11721441,Human_RBP_ID_22709763 4243 RMVar_ID_4243 Human_SNP_ID_453036127 A-to-I Human chr11 - 769560 769560 769560 TCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGTGGATCATCTGAAGTCAGGAGTTTG TCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGTGGATCATCTGAAGTCAGGAGTTTG T C GATD1 Ensembl:ENSG00000177225 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs989445981 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11721441,Human_RBP_ID_22709763 4244 RMVar_ID_4244 Human_SNP_ID_453036187 A-to-I Human chr11 - 769738 769738 769738 TGGCATGGTGGTGGGTGTGTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATGGCGTGAA TGGCATGGTGGTGGGTGTGTGTAGTCCCAGCTCCTTGGGAGGCTGAGGCAGGAGAATGGCGTGAA T G GATD1 Ensembl:ENSG00000177225 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs967177998 Functional Loss SNV dbSNP153 33..33 33 - - - 4245 RMVar_ID_4245 Human_SNP_ID_453036196 A-to-I Human chr11 - 769766 769763 769766 TAAAAAACAAAAATACAAAAAGTTAGCCTGGCATGGTGGTGGGTGTGTGTAGTCCCAGCTACTTG TAAAAAACAAAAATACAAAAAGTTAGCCTGGC___GTGGTGGGTGTGTGTAGTCCCAGCTACTTG CCAT C GATD1 Ensembl:ENSG00000177225 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1249077703 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_11721442,Human_RBP_ID_23155101 4246 RMVar_ID_4246 Human_SNP_ID_453036198 A-to-I Human chr11 - 769766 769766 769766 TAAAAAACAAAAATACAAAAAGTTAGCCTGGCATGGTGGTGGGTGTGTGTAGTCCCAGCTACTTG TAAAAAACAAAAATACAAAAAGTTAGCCTGGCGTGGTGGTGGGTGTGTGTAGTCCCAGCTACTTG T C GATD1 Ensembl:ENSG00000177225 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1032851568 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11721442,Human_RBP_ID_23155101 4247 RMVar_ID_4247 Human_SNP_ID_453036199 A-to-I Human chr11 - 769766 769766 769766 TAAAAAACAAAAATACAAAAAGTTAGCCTGGCATGGTGGTGGGTGTGTGTAGTCCCAGCTACTTG TAAAAAACAAAAATACAAAAAGTTAGCCTGGCCTGGTGGTGGGTGTGTGTAGTCCCAGCTACTTG T G GATD1 Ensembl:ENSG00000177225 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1032851568 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11721442,Human_RBP_ID_23155101 4248 RMVar_ID_4248 Human_SNP_ID_453036210 A-to-I Human chr11 - 769792 769791 769793 CTAACATGGTGAAACCCCATCTCTACTAAAAAACAAAAATACAAAAAGTTAGCCTGGCATGGTGG CTAACATGGTGAAACCCCATCTCTACTAAAA__CAAAAATACAAAAAGTTAGCCTGGCATGGTGG GTT G GATD1 Ensembl:ENSG00000177225 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1183921400 Functional Loss DEL dbSNP153 32..33 33 - - - 4249 RMVar_ID_4249 Human_SNP_ID_453036245 A-to-I Human chr11 - 769895 769895 769895 ACCGTTCAGTTGGGCCGGGCGCAGTGGCTCACACCTGTAACCCCAGCACTTTGGGAGGCCGAGGC ACCGTTCAGTTGGGCCGGGCGCAGTGGCTCACGCCTGTAACCCCAGCACTTTGGGAGGCCGAGGC T C GATD1 Ensembl:ENSG00000177225 Protein coding intron GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459,32596459 RNA-Seq:(High) rs1015669331 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22792279 4250 RMVar_ID_4250 Human_SNP_ID_453036248 A-to-I Human chr11 - 769905 769905 769905 TGATTATAAAACCGTTCAGTTGGGCCGGGCGCAGTGGCTCACACCTGTAACCCCAGCACTTTGGG TGATTATAAAACCGTTCAGTTGGGCCGGGCGCGGTGGCTCACACCTGTAACCCCAGCACTTTGGG T C GATD1 Ensembl:ENSG00000177225 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs961038415 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11721443 4251 RMVar_ID_4251 Human_SNP_ID_453038585 A-to-I Human chr11 - 776059 776059 776059 AGAATTGCTTGAGCCTGGAAGGTGGAGGTTGCAGTGAGCCGAGATCGCACCACTGCACTCCAGCC AGAATTGCTTGAGCCTGGAAGGTGGAGGTTGCGGTGAGCCGAGATCGCACCACTGCACTCCAGCC T C GATD1 Ensembl:ENSG00000177225 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1408880858 Functional Loss SNV dbSNP153 33..33 33 - - - 4252 RMVar_ID_4252 Human_SNP_ID_453039484 A-to-I Human chr11 + 778277 778277 778277 TTTTTTTGTGTTTTGGGTAGAGAGGGGGTCTCACTGTGTTGTCCAAGCTGGTCTCGAACTCCTGA TTTTTTTGTGTTTTGGGTAGAGAGGGGGTCTCTCTGTGTTGTCCAAGCTGGTCTCGAACTCCTGA A T AP006621.3 Ensembl:ENSG00000255284 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1325423120 Functional Loss SNV dbSNP153 33..33 33 - - - 4253 RMVar_ID_4253 Human_SNP_ID_453039502 A-to-I Human chr11 + 778341 778341 778341 ATCTAAAGCGATCTGCCTGCCTTGGCCTCCCAAAGTGCGAGGACTACAGGCGTGAGCCACCGCGC ATCTAAAGCGATCTGCCTGCCTTGGCCTCCCAGAGTGCGAGGACTACAGGCGTGAGCCACCGCGC A G AP006621.3 Ensembl:ENSG00000255284 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335942037 Functional Loss SNV dbSNP153 33..33 33 - - - 4254 RMVar_ID_4254 Human_SNP_ID_453039509 A-to-I Human chr11 + 778354 778354 778354 TGCCTGCCTTGGCCTCCCAAAGTGCGAGGACTACAGGCGTGAGCCACCGCGCCTGGCCTGAAGCA TGCCTGCCTTGGCCTCCCAAAGTGCGAGGACTGCAGGCGTGAGCCACCGCGCCTGGCCTGAAGCA A G AP006621.3 Ensembl:ENSG00000255284 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1462527636 Functional Loss SNV dbSNP153 33..33 33 - - - 4255 RMVar_ID_4255 Human_SNP_ID_453039687 A-to-I Human chr11 + 778864 778864 778864 GAACCCAGCGGGGGCAGAGGTTGCAATGAACCAAGATTGCGCCACTGCACTCCAGCCTGGGCGAC GAACCCAGCGGGGGCAGAGGTTGCAATGAACCCAGATTGCGCCACTGCACTCCAGCCTGGGCGAC A C AP006621.3 Ensembl:ENSG00000255284 lincRNA intron GSE100210;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T4 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs1383005019 Functional Loss SNV dbSNP153 33..33 33 - - - 4256 RMVar_ID_4256 Human_SNP_ID_453041575 A-to-I Human chr11 + 784301 784299 784301 TCTACTAAAAATACAAAAAAAAAAAAAAAATTAACCGGCTGTGGTGGCGAGTTCCTGTGGTCCCA TCTACTAAAAATACAAAAAAAAAAAAAAAAT__ACCGGCTGTGGTGGCGAGTTCCTGTGGTCCCA TTA T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1243089045 Functional Loss DEL dbSNP153 32..33 33 - - - 4257 RMVar_ID_4257 Human_SNP_ID_453041879 A-to-I Human chr11 + 785281 785280 785282 ATTTTCTTGGTGTTTTTGTTGTTGTTTGAGACAGGGTCTGGCTGTGTTGCCCAGGCTGGAGGGCA ATTTTCTTGGTGTTTTTGTTGTTGTTTGAGAC__GGTCTGGCTGTGTTGCCCAGGCTGGAGGGCA CAG C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1565029245 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_3381026,Human_RBP_ID_11728989 4258 RMVar_ID_4258 Human_SNP_ID_453063944 A-to-I Human chr11 - 840183 840183 840183 CTTTCAGAACCACTAAGGTCCCAGCCCTCACTAGGATGTCAGGAGCCAGGTCTAGGCCCAGCTTT CTTTCAGAACCACTAAGGTCCCAGCCCTCACTTGGATGTCAGGAGCCAGGTCTAGGCCCAGCTTT T A POLR2L Ensembl:ENSG00000177700 Protein coding intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1000676155 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_404975,Human_RBP_ID_6099629,Human_RBP_ID_8360186,Human_RBP_ID_11732100,Human_RBP_ID_17233281,Human_RBP_ID_22033844,Human_RBP_ID_23524167 Human_miRNA_ID_793007 4259 RMVar_ID_4259 Human_SNP_ID_453063945 A-to-I Human chr11 - 840183 840183 840183 CTTTCAGAACCACTAAGGTCCCAGCCCTCACTAGGATGTCAGGAGCCAGGTCTAGGCCCAGCTTT CTTTCAGAACCACTAAGGTCCCAGCCCTCACTGGGATGTCAGGAGCCAGGTCTAGGCCCAGCTTT T C POLR2L Ensembl:ENSG00000177700 Protein coding intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1000676155 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_404975,Human_RBP_ID_6099629,Human_RBP_ID_8360186,Human_RBP_ID_11732100,Human_RBP_ID_17233281,Human_RBP_ID_22033844,Human_RBP_ID_23524167 Human_miRNA_ID_793007 4260 RMVar_ID_4260 Human_SNP_ID_453074538 A-to-I Human chr11 - 868361 868361 868361 ATGGTGGCATGTGCCTGTACTCCTGGCTACTCAGGAGGCTGAGATGGGAGGATCGCTTGATGAGG ATGGTGGCATGTGCCTGTACTCCTGGCTACTCGGGAGGCTGAGATGGGAGGATCGCTTGATGAGG T C CHID1 Ensembl:ENSG00000177830 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355179708 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_405477 RMVar_hsa_circ_92271,RMVar_hsa_circ_147494 4261 RMVar_ID_4261 Human_SNP_ID_453076474 A-to-I Human chr11 - 874380 874380 874380 CAGCTCACTGTAGCCTCCACCTCCCAGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGCT CAGCTCACTGTAGCCTCCACCTCCCAGGTTCAGGTGATTCTCCTGCCTCAGCCTCCCAAGTAGCT T C CHID1 Ensembl:ENSG00000177830 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1460936135 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_147495,RMVar_hsa_circ_147496 4262 RMVar_ID_4262 Human_SNP_ID_453078553 A-to-I Human chr11 - 881799 881799 881799 CAGGGTTTTGCCATGTTGTCGAGGCTGGTCTCAAATTCCTAGGCTCAAGCGATCCTCCTGCCTCA CAGGGTTTTGCCATGTTGTCGAGGCTGGTCTCGAATTCCTAGGCTCAAGCGATCCTCCTGCCTCA T C CHID1 Ensembl:ENSG00000177830 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335331668 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11742701 RMVar_hsa_circ_109655,RMVar_hsa_circ_92271,RMVar_hsa_circ_116638,RMVar_hsa_circ_147494,RMVar_hsa_circ_147495,RMVar_hsa_circ_147496 4263 RMVar_ID_4263 Human_SNP_ID_453079855 A-to-I Human chr11 - 885837 885837 885837 ATTTTTCCTTTTTGAATCAACTAAAAAAGGCAAGAGGATTGCTTGAGCCCAGAAGTTCAAGGCTG ATTTTTCCTTTTTGAATCAACTAAAAAAGGCATGAGGATTGCTTGAGCCCAGAAGTTCAAGGCTG T A CHID1 Ensembl:ENSG00000177830 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1370483590 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 4264 RMVar_ID_4264 Human_SNP_ID_453085014 A-to-I Human chr11 - 902314 902314 902314 CTCCATCTTTTGCCAGTGGAACAGCCATGGCTACGATGTCACCAAGGTCTTTGGGAGCAAGTTCA CTCCATCTTTTGCCAGTGGAACAGCCATGGCTGCGATGTCACCAAGGTCTTTGGGAGCAAGTTCA T C CHID1 Ensembl:ENSG00000177830 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs775559505 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_865668,Human_RBP_ID_4181568,Human_RBP_ID_18971642,Human_RBP_ID_22754526 Human_Splice_Rec_1196322,Human_Splice_Rec_1196346,Human_Splice_Rec_1196370,Human_Splice_Rec_1196418,Human_Splice_Rec_1196442,Human_Splice_Rec_1196466,Human_Splice_Rec_1196498,Human_Splice_Rec_1196532,Human_Splice_Rec_1196533,Human_Splice_Rec_1196542,Human_Splice_Rec_1196560,Human_Splice_Rec_1196572,Human_Splice_Rec_1196578,Human_Splice_Rec_1196584 RMVar_hsa_circ_57161,RMVar_hsa_circ_351970,RMVar_hsa_circ_356879,RMVar_hsa_circ_365575,RMVar_hsa_circ_359857,RMVar_hsa_circ_49203,RMVar_hsa_circ_359756,RMVar_hsa_circ_375919,RMVar_hsa_circ_147500 4265 RMVar_ID_4265 Human_SNP_ID_453092500 A-to-I Human chr11 + 927245 927245 927245 CACCATGCCTGGCTGATTTTCGTGTTTTTTGTAGAGATGGGGGGGTCTCGCCATGTTGCCTAGGC CACCATGCCTGGCTGATTTTCGTGTTTTTTGTGGAGATGGGGGGGTCTCGCCATGTTGCCTAGGC A G AP2A2 Ensembl:ENSG00000183020 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1565221212 Functional Loss SNV dbSNP153 33..33 33 - - - 4266 RMVar_ID_4266 Human_SNP_ID_453101887 A-to-I Human chr11 + 960841 960841 960841 CACCCCACACGGCTGGTTTTTGTATTTTTAGTAGAGACGGGGGTTTCTCCATGTTGGTCAGGCTG CACCCCACACGGCTGGTTTTTGTATTTTTAGTGGAGACGGGGGTTTCTCCATGTTGGTCAGGCTG A G AP2A2 Ensembl:ENSG00000183020 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs537310787 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_292644 4267 RMVar_ID_4267 Human_SNP_ID_453102706 A-to-I Human chr11 + 963648 963648 963648 GTTGATCAATTGATTGATCTATTGATTTACTGAGACAAGATCTTGCTCTGTTGACCAGGCTGCCC GTTGATCAATTGATTGATCTATTGATTTACTGCGACAAGATCTTGCTCTGTTGACCAGGCTGCCC A C AP2A2 Ensembl:ENSG00000183020 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1214770867 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_292644 4268 RMVar_ID_4268 Human_SNP_ID_453109238 A-to-I Human chr11 + 985482 985482 985482 GCCGCCTGACTGAGTGCCTGGAGACCATCCTGAACAAAGCCCAAGAACCGCCCAAGTCGAAGAAG GCCGCCTGACTGAGTGCCTGGAGACCATCCTGGACAAAGCCCAAGAACCGCCCAAGTCGAAGAAG A G AP2A2 Ensembl:ENSG00000183020 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1364913203 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_864736,Human_RBP_ID_3938833,Human_RBP_ID_11759241,Human_RBP_ID_26319489 Human_Splice_Rec_1196616,Human_Splice_Rec_1196660,Human_Splice_Rec_1196692,Human_Splice_Rec_1196706,Human_Splice_Rec_1196722 RMVar_hsa_circ_114519,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_103735,RMVar_hsa_circ_147508,RMVar_hsa_circ_147507,RMVar_hsa_circ_376464,RMVar_hsa_circ_147509 4269 RMVar_ID_4269 Human_SNP_ID_453194276 A-to-I Human chr11 + 1232750 1232750 1232750 CGCCTGTGCCGCCAAGGGCGTACAGCTCAGCGACTGGAGGGACGGCGTCTGCAGTGAGTGCCCAC CGCCTGTGCCGCCAAGGGCGTACAGCTCAGCGGCTGGAGGGACGGCGTCTGCAGTGAGTGCCCAC A G MUC5B Ensembl:ENSG00000117983 Protein coding exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs202127660 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_Splice_Rec_1197137,Human_Splice_Rec_1197185 4270 RMVar_ID_4270 Human_SNP_ID_453263208 A-to-I Human chr11 + 1448505 1448505 1448505 TGCCCCAGCAACTGTAGCTCAGTGTTCCCAGCAGCTGCCTGGCCGGATAGGACCAGGGCTCGGCC TGCCCCAGCAACTGTAGCTCAGTGTTCCCAGCCGCTGCCTGGCCGGATAGGACCAGGGCTCGGCC A C BRSK2 Ensembl:ENSG00000174672 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1445272385 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266764 4271 RMVar_ID_4271 Human_SNP_ID_453271670 A-to-I Human chr11 - 1469568 1469568 1469568 CCAAGGAACACCCATGGTGCAGTCCTCAGGCAAGGCCAGGACGGGGCTGAGGCCCTGCGTGGAGA CCAAGGAACACCCATGGTGCAGTCCTCAGGCAGGGCCAGGACGGGGCTGAGGCCCTGCGTGGAGA T C MOB2 Ensembl:ENSG00000182208 Protein coding exon GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs984948705 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_147530,RMVar_hsa_circ_104097 4272 RMVar_ID_4272 Human_SNP_ID_453302925 A-to-I Human chr11 + 1576039 1576039 1576039 ACCACGCCCATCTAAATTTTGTATTTTTTAGTAGAGATTGGGTTTCACCACGTTGGCCAGGCTCG ACCACGCCCATCTAAATTTTGTATTTTTTAGTGGAGATTGGGTTTCACCACGTTGGCCAGGCTCG A G KRTAP5-AS1 Ensembl:ENSG00000233930 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs570169434 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5246027,Human_RBP_ID_8247254 4273 RMVar_ID_4273 Human_SNP_ID_453305014 A-to-I Human chr11 + 1582897 1582897 1582897 ATCTCTACTAAAAATACAAACAAAACAAAATTAGCTGGGCATGGTGGCTCATGCCTGTAGTCCCA ATCTCTACTAAAAATACAAACAAAACAAAATTGGCTGGGCATGGTGGCTCATGCCTGTAGTCCCA A G KRTAP5-AS1 Ensembl:ENSG00000233930 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1217225097 Functional Loss SNV dbSNP153 33..33 33 - - - 4274 RMVar_ID_4274 Human_SNP_ID_453425388 A-to-I Human chr11 + 1981520 1981519 1981521 GCTGGGCCTTCAGGCACAGGGGAGGGTGGCTCAGGGGCCAGCAGCAGACGTTGGTGCCTGCCCCT GCTGGGCCTTCAGGCACAGGGGAGGGTGGCTC__GGGCCAGCAGCAGACGTTGGTGCCTGCCCCT CAG C MRPL23 Ensembl:ENSG00000214026 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1176320419 Functional Loss DEL dbSNP153 33..34 33 - - - 4275 RMVar_ID_4275 Human_SNP_ID_453425393 A-to-I Human chr11 + 1981527 1981527 1981527 CTTCAGGCACAGGGGAGGGTGGCTCAGGGGCCAGCAGCAGACGTTGGTGCCTGCCCCTGCAGCGG CTTCAGGCACAGGGGAGGGTGGCTCAGGGGCCCGCAGCAGACGTTGGTGCCTGCCCCTGCAGCGG A C MRPL23 Ensembl:ENSG00000214026 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs770161845 Functional Loss SNV dbSNP153 33..33 33 - - - 4276 RMVar_ID_4276 Human_SNP_ID_453429378 A-to-I Human chr11 - 1996783 1996783 1996783 GAGAGGGCCCACAGTGGACTTGGTGACGCTGTATGCCCTCACCGCTCAGCCCCTGGGGCTGGCTT GAGAGGGCCCACAGTGGACTTGGTGACGCTGTGTGCCCTCACCGCTCAGCCCCTGGGGCTGGCTT T C MIR675,H19 Ensembl:ENSG00000284010,Ensembl:ENSG00000130600 miRNA,lincRNA exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1160118501 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5169113,Human_RBP_ID_5415810,Human_RBP_ID_5436279,Human_RBP_ID_5460149,Human_RBP_ID_5489409,Human_RBP_ID_5550887 Human_miRNA_ID_2695680,Human_miRNA_ID_3190744 RMVar_hsa_circ_116698,RMVar_hsa_circ_147551,RMVar_hsa_circ_128033,RMVar_hsa_circ_147555 4277 RMVar_ID_4277 Human_SNP_ID_453694758 A-to-I Human chr11 - 2944852 2944852 2944852 CTTCCTAGCAGGCGCAAGGCCTGTGCGGAAGAAACGCCGCTCCCTGCCACCAGGGCTGAAGATGC CTTCCTAGCAGGCGCAAGGCCTGTGCGGAAGATACGCCGCTCCCTGCCACCAGGGCTGAAGATGC T A NAP1L4 Ensembl:ENSG00000205531 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1445613749 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_394406,Human_RBP_ID_5110342,Human_RBP_ID_22160903 RMVar_hsa_circ_77496,RMVar_hsa_circ_126801,RMVar_hsa_circ_104267,RMVar_hsa_circ_147580,RMVar_hsa_circ_147581,RMVar_hsa_circ_147582 4278 RMVar_ID_4278 Human_SNP_ID_453701681 A-to-I Human chr11 - 2969171 2969171 2969171 GCCTGGGCAGCATCGCGAAATCCCATCTCTACAAAAAATAGAAAAGTTAGCTGGGCGTTGTGGTG GCCTGGGCAGCATCGCGAAATCCCATCTCTACGAAAAATAGAAAAGTTAGCTGGGCGTTGTGGTG T C NAP1L4 Ensembl:ENSG00000205531 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1564982984 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11592072 RMVar_hsa_circ_73830,RMVar_hsa_circ_104267,RMVar_hsa_circ_267453,RMVar_hsa_circ_147582,RMVar_hsa_circ_329952,RMVar_hsa_circ_377271,RMVar_hsa_circ_102046,RMVar_hsa_circ_85042,RMVar_hsa_circ_147584,RMVar_hsa_circ_147585,RMVar_hsa_circ_297978,RMVar_hsa_circ_147591,RMVar_hsa_circ_147587,RMVar_hsa_circ_147588,RMVar_hsa_circ_147589,RMVar_hsa_circ_375028,RMVar_hsa_circ_326691,RMVar_hsa_circ_344702,RMVar_hsa_circ_8318,RMVar_hsa_circ_46688,RMVar_hsa_circ_147593,RMVar_hsa_circ_147594 4279 RMVar_ID_4279 Human_SNP_ID_453701682 A-to-I Human chr11 - 2969173 2969173 2969173 CAGCCTGGGCAGCATCGCGAAATCCCATCTCTACAAAAAATAGAAAAGTTAGCTGGGCGTTGTGG CAGCCTGGGCAGCATCGCGAAATCCCATCTCTGCAAAAAATAGAAAAGTTAGCTGGGCGTTGTGG T C NAP1L4 Ensembl:ENSG00000205531 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1325377586 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11592072 RMVar_hsa_circ_73830,RMVar_hsa_circ_104267,RMVar_hsa_circ_267453,RMVar_hsa_circ_147582,RMVar_hsa_circ_329952,RMVar_hsa_circ_377271,RMVar_hsa_circ_102046,RMVar_hsa_circ_85042,RMVar_hsa_circ_147584,RMVar_hsa_circ_147585,RMVar_hsa_circ_297978,RMVar_hsa_circ_147591,RMVar_hsa_circ_147587,RMVar_hsa_circ_147588,RMVar_hsa_circ_147589,RMVar_hsa_circ_375028,RMVar_hsa_circ_326691,RMVar_hsa_circ_344702,RMVar_hsa_circ_8318,RMVar_hsa_circ_46688,RMVar_hsa_circ_147593,RMVar_hsa_circ_147594 4280 RMVar_ID_4280 Human_SNP_ID_453705005 A-to-I Human chr11 - 2980413 2980413 2980413 GGTAGGCTGAGGTGGGAGGATCTCTTGAGGCCAGGAGTTTGGGACTCAGCCTGGGCAACTTAGCC GGTAGGCTGAGGTGGGAGGATCTCTTGAGGCCGGGAGTTTGGGACTCAGCCTGGGCAACTTAGCC T C NAP1L4 Ensembl:ENSG00000205531 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs547435422 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11592705 RMVar_hsa_circ_104267,RMVar_hsa_circ_147582,RMVar_hsa_circ_102046,RMVar_hsa_circ_147585,RMVar_hsa_circ_6937,RMVar_hsa_circ_46688,RMVar_hsa_circ_349725 4281 RMVar_ID_4281 Human_SNP_ID_453705006 A-to-I Human chr11 - 2980413 2980413 2980413 GGTAGGCTGAGGTGGGAGGATCTCTTGAGGCCAGGAGTTTGGGACTCAGCCTGGGCAACTTAGCC GGTAGGCTGAGGTGGGAGGATCTCTTGAGGCCCGGAGTTTGGGACTCAGCCTGGGCAACTTAGCC T G NAP1L4 Ensembl:ENSG00000205531 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs547435422 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11592705 RMVar_hsa_circ_104267,RMVar_hsa_circ_147582,RMVar_hsa_circ_102046,RMVar_hsa_circ_147585,RMVar_hsa_circ_6937,RMVar_hsa_circ_46688,RMVar_hsa_circ_349725 4282 RMVar_ID_4282 Human_SNP_ID_453705020 A-to-I Human chr11 - 2980452 2980452 2980452 GCCAGGCGTGTTGACTCACACCTGTAATCCCAACACTTTGGTAGGCTGAGGTGGGAGGATCTCTT GCCAGGCGTGTTGACTCACACCTGTAATCCCAGCACTTTGGTAGGCTGAGGTGGGAGGATCTCTT T C NAP1L4 Ensembl:ENSG00000205531 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1454433986 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104267,RMVar_hsa_circ_147582,RMVar_hsa_circ_102046,RMVar_hsa_circ_147585,RMVar_hsa_circ_6937,RMVar_hsa_circ_46688,RMVar_hsa_circ_349725 4283 RMVar_ID_4283 Human_SNP_ID_453705023 A-to-I Human chr11 - 2980458 2980458 2980458 GTATAGGCCAGGCGTGTTGACTCACACCTGTAATCCCAACACTTTGGTAGGCTGAGGTGGGAGGA GTATAGGCCAGGCGTGTTGACTCACACCTGTATTCCCAACACTTTGGTAGGCTGAGGTGGGAGGA T A NAP1L4 Ensembl:ENSG00000205531 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs181731524 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104267,RMVar_hsa_circ_147582,RMVar_hsa_circ_102046,RMVar_hsa_circ_147585,RMVar_hsa_circ_6937,RMVar_hsa_circ_46688,RMVar_hsa_circ_349725 4284 RMVar_ID_4284 Human_SNP_ID_453705203 A-to-I Human chr11 - 2981064 2981064 2981064 CTGGCTAATTTTGTTTGTTTGTTTGTTTTTGTAGAGACGAGGTTTCCCCATGTTGCCCAGGCTGG CTGGCTAATTTTGTTTGTTTGTTTGTTTTTGTGGAGACGAGGTTTCCCCATGTTGCCCAGGCTGG T C NAP1L4 Ensembl:ENSG00000205531 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404775902 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3373356,Human_RBP_ID_6066115,Human_RBP_ID_11592746 RMVar_hsa_circ_104267,RMVar_hsa_circ_147582,RMVar_hsa_circ_102046,RMVar_hsa_circ_147585,RMVar_hsa_circ_6937,RMVar_hsa_circ_46688,RMVar_hsa_circ_349725 4285 RMVar_ID_4285 Human_SNP_ID_453705971 A-to-I Human chr11 - 2983492 2983492 2983492 ACATGCCGGGCTGGGCATGGTGCCTCTGTCCTATAATCCCAGCACTTTGAGAGGCTAAGGTGGGA ACATGCCGGGCTGGGCATGGTGCCTCTGTCCTGTAATCCCAGCACTTTGAGAGGCTAAGGTGGGA T C NAP1L4 Ensembl:ENSG00000205531 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs903704657 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11592890,Human_RBP_ID_17794306 RMVar_hsa_circ_104267,RMVar_hsa_circ_147582,RMVar_hsa_circ_102046,RMVar_hsa_circ_147585,RMVar_hsa_circ_6937,RMVar_hsa_circ_46688,RMVar_hsa_circ_349725 4286 RMVar_ID_4286 Human_SNP_ID_453737656 A-to-I Human chr11 - 3096427 3096427 3096427 TTTAGTAGAGATAGGGTTTCACCATGTTGGCCAGGCTGGTCACAAACTCCTGCCCTCAGGTGATC TTTAGTAGAGATAGGGTTTCACCATGTTGGCCGGGCTGGTCACAAACTCCTGCCCTCAGGTGATC T C OSBPL5 Ensembl:ENSG00000021762 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1233077157 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_147612,RMVar_hsa_circ_147611,RMVar_hsa_circ_99648,RMVar_hsa_circ_375574 4287 RMVar_ID_4287 Human_SNP_ID_453743730 A-to-I Human chr11 - 3113463 3113463 3113463 TTTAGTAGAGATGGGGTTTCACTATGTTGGCCAGACTGGTCTTGAACTCCTGACTTTGTGATCCA TTTAGTAGAGATGGGGTTTCACTATGTTGGCCGGACTGGTCTTGAACTCCTGACTTTGTGATCCA T C OSBPL5 Ensembl:ENSG00000021762 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1158110799 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 4288 RMVar_ID_4288 Human_SNP_ID_453743740 A-to-I Human chr11 - 3113492 3113492 3113492 TGCCAACACACCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACTATGTTGGCCAGAC TGCCAACACACCTGGCTAATTTTTGTATTTTTGGTAGAGATGGGGTTTCACTATGTTGGCCAGAC T C OSBPL5 Ensembl:ENSG00000021762 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1197734810 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 4289 RMVar_ID_4289 Human_SNP_ID_453743753 A-to-I Human chr11 - 3113533 3113533 3113533 CTCCTGCCTCAGCCTCACGAGTAGCTGGGATTACAGGTGCCTGCCAACACACCTGGCTAATTTTT CTCCTGCCTCAGCCTCACGAGTAGCTGGGATTGCAGGTGCCTGCCAACACACCTGGCTAATTTTT T C OSBPL5 Ensembl:ENSG00000021762 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1364751238 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 4290 RMVar_ID_4290 Human_SNP_ID_453745081 A-to-I Human chr11 - 3118703 3118703 3118703 GCTGGGCATGGTGGTGGGTGCCCGTGATCCCAACTACTCAGGAGGCTGAGGCAAGAGAATCCCTT GCTGGGCATGGTGGTGGGTGCCCGTGATCCCAGCTACTCAGGAGGCTGAGGCAAGAGAATCCCTT T C OSBPL5 Ensembl:ENSG00000021762 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs373175185 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 4291 RMVar_ID_4291 Human_SNP_ID_453853524 A-to-I Human chr11 + 3529935 3529935 3529935 CCTGGTCAACATGGTGGAACCCCATCTCTACTAAATATCCCAAAATTAGCCAGGTGTGGCGGATG CCTGGTCAACATGGTGGAACCCCATCTCTACTCAATATCCCAAAATTAGCCAGGTGTGGCGGATG A C AC127526.1 Ensembl:ENSG00000254757 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1413198564 Functional Loss SNV dbSNP153 33..33 33 - - - 4292 RMVar_ID_4292 Human_SNP_ID_453902577 A-to-I Human chr11 - 3687229 3687229 3687229 ACTCTGAAAATTCAGTAATAAGAAAACAGGCCAGGTATGGTGCGTCATGCCTATAATCCCAGCAG ACTCTGAAAATTCAGTAATAAGAAAACAGGCCCGGTATGGTGCGTCATGCCTATAATCCCAGCAG T G NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1322376919 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_147644,RMVar_hsa_circ_147645 4293 RMVar_ID_4293 Human_SNP_ID_453902758 A-to-I Human chr11 - 3687863 3687863 3687863 ACTGCACCCAGCCTTGTTTTGTTAGCCAAGATAGTCTCGATCTCCTGACCTCGTGATCCACCCGC ACTGCACCCAGCCTTGTTTTGTTAGCCAAGATGGTCTCGATCTCCTGACCTCGTGATCCACCCGC T C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1051430714 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_147644,RMVar_hsa_circ_147645 4294 RMVar_ID_4294 Human_SNP_ID_453903219 A-to-I Human chr11 - 3689283 3689283 3689283 TGACCTCGTGATCTGCCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGCGAGCCACTGCAC TGACCTCGTGATCTGCCCACCTCAGCCTCCCAGAGTGCTGGGATTACAGGCGCGAGCCACTGCAC T C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1032792598 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_147644,RMVar_hsa_circ_147645 4295 RMVar_ID_4295 Human_SNP_ID_453903388 A-to-I Human chr11 - 3689903 3689903 3689903 GCCAGCCATGGTGGCTCACACCTGTAATCCCAACACTTTGGAAGGCCAAGGCCAGCAGATCACTT GCCAGCCATGGTGGCTCACACCTGTAATCCCAGCACTTTGGAAGGCCAAGGCCAGCAGATCACTT T C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1426412049 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_147644,RMVar_hsa_circ_147645 4296 RMVar_ID_4296 Human_SNP_ID_453905930 A-to-I Human chr11 - 3698419 3698419 3698419 CCAGCCGAACTATGTCTTCTAATTCTTTTTTTAGGACCTTAAACATTGTTTACTTGATTAAAATT CCAGCCGAACTATGTCTTCTAATTCTTTTTTTGGGACCTTAAACATTGTTTACTTGATTAAAATT T C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs553058466 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35,RMVar_hsa_circ_75074,RMVar_hsa_circ_147634,RMVar_hsa_circ_367828,RMVar_hsa_circ_108806,RMVar_hsa_circ_106647,RMVar_hsa_circ_147635,RMVar_hsa_circ_75213,RMVar_hsa_circ_379094,RMVar_hsa_circ_147638,RMVar_hsa_circ_35304,RMVar_hsa_circ_121348,RMVar_hsa_circ_125364,RMVar_hsa_circ_104783,RMVar_hsa_circ_147640,RMVar_hsa_circ_52316,RMVar_hsa_circ_70296,RMVar_hsa_circ_147641,RMVar_hsa_circ_114245,RMVar_hsa_circ_147639,RMVar_hsa_circ_354108,RMVar_hsa_circ_47819,RMVar_hsa_circ_147645,RMVar_hsa_circ_307900,RMVar_hsa_circ_321289,RMVar_hsa_circ_281516,RMVar_hsa_circ_109406,RMVar_hsa_circ_97527,RMVar_hsa_circ_11860,RMVar_hsa_circ_37210,RMVar_hsa_circ_6580,RMVar_hsa_circ_20849,RMVar_hsa_circ_71064,RMVar_hsa_circ_147649,RMVar_hsa_circ_147651,RMVar_hsa_circ_147652,RMVar_hsa_circ_147650,RMVar_hsa_circ_334660,RMVar_hsa_circ_349447,RMVar_hsa_circ_17317,RMVar_hsa_circ_49012,RMVar_hsa_circ_147653,RMVar_hsa_circ_374437,RMVar_hsa_circ_77589,RMVar_hsa_circ_304287,RMVar_hsa_circ_51322,RMVar_hsa_circ_147655,RMVar_hsa_circ_147656,RMVar_hsa_circ_147654 4297 RMVar_ID_4297 Human_SNP_ID_453905932 A-to-I Human chr11 - 3698430 3698430 3698430 AGCCACTGCACCCAGCCGAACTATGTCTTCTAATTCTTTTTTTAGGACCTTAAACATTGTTTACT AGCCACTGCACCCAGCCGAACTATGTCTTCTAGTTCTTTTTTTAGGACCTTAAACATTGTTTACT T C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037225834 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11613564 RMVar_hsa_circ_35,RMVar_hsa_circ_75074,RMVar_hsa_circ_147634,RMVar_hsa_circ_367828,RMVar_hsa_circ_108806,RMVar_hsa_circ_106647,RMVar_hsa_circ_147635,RMVar_hsa_circ_75213,RMVar_hsa_circ_379094,RMVar_hsa_circ_147638,RMVar_hsa_circ_35304,RMVar_hsa_circ_121348,RMVar_hsa_circ_125364,RMVar_hsa_circ_104783,RMVar_hsa_circ_147640,RMVar_hsa_circ_52316,RMVar_hsa_circ_70296,RMVar_hsa_circ_147641,RMVar_hsa_circ_114245,RMVar_hsa_circ_147639,RMVar_hsa_circ_354108,RMVar_hsa_circ_47819,RMVar_hsa_circ_147645,RMVar_hsa_circ_307900,RMVar_hsa_circ_321289,RMVar_hsa_circ_281516,RMVar_hsa_circ_109406,RMVar_hsa_circ_97527,RMVar_hsa_circ_11860,RMVar_hsa_circ_37210,RMVar_hsa_circ_6580,RMVar_hsa_circ_20849,RMVar_hsa_circ_71064,RMVar_hsa_circ_147649,RMVar_hsa_circ_147651,RMVar_hsa_circ_147652,RMVar_hsa_circ_147650,RMVar_hsa_circ_334660,RMVar_hsa_circ_349447,RMVar_hsa_circ_17317,RMVar_hsa_circ_49012,RMVar_hsa_circ_147653,RMVar_hsa_circ_374437,RMVar_hsa_circ_77589,RMVar_hsa_circ_304287,RMVar_hsa_circ_51322,RMVar_hsa_circ_147655,RMVar_hsa_circ_147656,RMVar_hsa_circ_147654 4298 RMVar_ID_4298 Human_SNP_ID_453906073 A-to-I Human chr11 - 3698897 3698897 3698897 ATGTAATATAACATAAAATTTAACTTTTAATCAAGTAAACAATGTTTAAGGTCCTAAACAGAGAA ATGTAATATAACATAAAATTTAACTTTTAATCGAGTAAACAATGTTTAAGGTCCTAAACAGAGAA T C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs533806398 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11613565 RMVar_hsa_circ_35,RMVar_hsa_circ_75074,RMVar_hsa_circ_147634,RMVar_hsa_circ_367828,RMVar_hsa_circ_108806,RMVar_hsa_circ_106647,RMVar_hsa_circ_147635,RMVar_hsa_circ_75213,RMVar_hsa_circ_379094,RMVar_hsa_circ_147638,RMVar_hsa_circ_35304,RMVar_hsa_circ_121348,RMVar_hsa_circ_125364,RMVar_hsa_circ_104783,RMVar_hsa_circ_147640,RMVar_hsa_circ_52316,RMVar_hsa_circ_70296,RMVar_hsa_circ_147641,RMVar_hsa_circ_114245,RMVar_hsa_circ_147639,RMVar_hsa_circ_354108,RMVar_hsa_circ_47819,RMVar_hsa_circ_147645,RMVar_hsa_circ_307900,RMVar_hsa_circ_321289,RMVar_hsa_circ_281516,RMVar_hsa_circ_109406,RMVar_hsa_circ_97527,RMVar_hsa_circ_11860,RMVar_hsa_circ_37210,RMVar_hsa_circ_6580,RMVar_hsa_circ_20849,RMVar_hsa_circ_71064,RMVar_hsa_circ_147649,RMVar_hsa_circ_147651,RMVar_hsa_circ_147652,RMVar_hsa_circ_147650,RMVar_hsa_circ_334660,RMVar_hsa_circ_349447,RMVar_hsa_circ_17317,RMVar_hsa_circ_49012,RMVar_hsa_circ_147653,RMVar_hsa_circ_374437,RMVar_hsa_circ_77589,RMVar_hsa_circ_304287,RMVar_hsa_circ_51322,RMVar_hsa_circ_147655,RMVar_hsa_circ_147656,RMVar_hsa_circ_147654 4299 RMVar_ID_4299 Human_SNP_ID_453906077 A-to-I Human chr11 - 3698901 3698901 3698901 GAATATGTAATATAACATAAAATTTAACTTTTAATCAAGTAAACAATGTTTAAGGTCCTAAACAG GAATATGTAATATAACATAAAATTTAACTTTTTATCAAGTAAACAATGTTTAAGGTCCTAAACAG T A NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1367188190 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11613565 RMVar_hsa_circ_35,RMVar_hsa_circ_75074,RMVar_hsa_circ_147634,RMVar_hsa_circ_367828,RMVar_hsa_circ_108806,RMVar_hsa_circ_106647,RMVar_hsa_circ_147635,RMVar_hsa_circ_75213,RMVar_hsa_circ_379094,RMVar_hsa_circ_147638,RMVar_hsa_circ_35304,RMVar_hsa_circ_121348,RMVar_hsa_circ_125364,RMVar_hsa_circ_104783,RMVar_hsa_circ_147640,RMVar_hsa_circ_52316,RMVar_hsa_circ_70296,RMVar_hsa_circ_147641,RMVar_hsa_circ_114245,RMVar_hsa_circ_147639,RMVar_hsa_circ_354108,RMVar_hsa_circ_47819,RMVar_hsa_circ_147645,RMVar_hsa_circ_307900,RMVar_hsa_circ_321289,RMVar_hsa_circ_281516,RMVar_hsa_circ_109406,RMVar_hsa_circ_97527,RMVar_hsa_circ_11860,RMVar_hsa_circ_37210,RMVar_hsa_circ_6580,RMVar_hsa_circ_20849,RMVar_hsa_circ_71064,RMVar_hsa_circ_147649,RMVar_hsa_circ_147651,RMVar_hsa_circ_147652,RMVar_hsa_circ_147650,RMVar_hsa_circ_334660,RMVar_hsa_circ_349447,RMVar_hsa_circ_17317,RMVar_hsa_circ_49012,RMVar_hsa_circ_147653,RMVar_hsa_circ_374437,RMVar_hsa_circ_77589,RMVar_hsa_circ_304287,RMVar_hsa_circ_51322,RMVar_hsa_circ_147655,RMVar_hsa_circ_147656,RMVar_hsa_circ_147654 4300 RMVar_ID_4300 Human_SNP_ID_453906083 A-to-I Human chr11 - 3698917 3698917 3698917 ATTGCTGGTTCCCGTGGAATATGTAATATAACATAAAATTTAACTTTTAATCAAGTAAACAATGT ATTGCTGGTTCCCGTGGAATATGTAATATAACGTAAAATTTAACTTTTAATCAAGTAAACAATGT T C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs938851531 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35,RMVar_hsa_circ_75074,RMVar_hsa_circ_147634,RMVar_hsa_circ_367828,RMVar_hsa_circ_108806,RMVar_hsa_circ_106647,RMVar_hsa_circ_147635,RMVar_hsa_circ_75213,RMVar_hsa_circ_379094,RMVar_hsa_circ_147638,RMVar_hsa_circ_35304,RMVar_hsa_circ_121348,RMVar_hsa_circ_125364,RMVar_hsa_circ_104783,RMVar_hsa_circ_147640,RMVar_hsa_circ_52316,RMVar_hsa_circ_70296,RMVar_hsa_circ_147641,RMVar_hsa_circ_114245,RMVar_hsa_circ_147639,RMVar_hsa_circ_354108,RMVar_hsa_circ_47819,RMVar_hsa_circ_147645,RMVar_hsa_circ_307900,RMVar_hsa_circ_321289,RMVar_hsa_circ_281516,RMVar_hsa_circ_109406,RMVar_hsa_circ_97527,RMVar_hsa_circ_11860,RMVar_hsa_circ_37210,RMVar_hsa_circ_6580,RMVar_hsa_circ_20849,RMVar_hsa_circ_71064,RMVar_hsa_circ_147649,RMVar_hsa_circ_147651,RMVar_hsa_circ_147652,RMVar_hsa_circ_147650,RMVar_hsa_circ_334660,RMVar_hsa_circ_349447,RMVar_hsa_circ_17317,RMVar_hsa_circ_49012,RMVar_hsa_circ_147653,RMVar_hsa_circ_374437,RMVar_hsa_circ_77589,RMVar_hsa_circ_304287,RMVar_hsa_circ_51322,RMVar_hsa_circ_147655,RMVar_hsa_circ_147656,RMVar_hsa_circ_147654 4301 RMVar_ID_4301 Human_SNP_ID_453906956 A-to-I Human chr11 - 3701814 3701810 3701815 GGGCGTTGTGGCAGGCGCCTGTAGACCCAGCTAGTCAGGAGGCTGAGGCAGGAGAATGGTGTGAA GGGCGTTGTGGCAGGCGCCTGTAGACCCAGC_____AGGAGGCTGAGGCAGGAGAATGGTGTGAA TGACTA T NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1335296801 Functional Loss DEL dbSNP153 32..36 33 - - - RMVar_hsa_circ_75074,RMVar_hsa_circ_147634,RMVar_hsa_circ_367828,RMVar_hsa_circ_108806,RMVar_hsa_circ_106647,RMVar_hsa_circ_147635,RMVar_hsa_circ_75213,RMVar_hsa_circ_147638,RMVar_hsa_circ_35304,RMVar_hsa_circ_121348,RMVar_hsa_circ_125364,RMVar_hsa_circ_104783,RMVar_hsa_circ_147640,RMVar_hsa_circ_52316,RMVar_hsa_circ_147641,RMVar_hsa_circ_114245,RMVar_hsa_circ_147639,RMVar_hsa_circ_47819,RMVar_hsa_circ_147645,RMVar_hsa_circ_307900,RMVar_hsa_circ_321289,RMVar_hsa_circ_109406,RMVar_hsa_circ_97527,RMVar_hsa_circ_11860,RMVar_hsa_circ_37210,RMVar_hsa_circ_6580,RMVar_hsa_circ_9340,RMVar_hsa_circ_20849,RMVar_hsa_circ_71064,RMVar_hsa_circ_147651,RMVar_hsa_circ_147652,RMVar_hsa_circ_147650,RMVar_hsa_circ_349447,RMVar_hsa_circ_17317,RMVar_hsa_circ_374437,RMVar_hsa_circ_77589,RMVar_hsa_circ_51322,RMVar_hsa_circ_106281,RMVar_hsa_circ_147655,RMVar_hsa_circ_147654,RMVar_hsa_circ_361127,RMVar_hsa_circ_74486,RMVar_hsa_circ_147657,RMVar_hsa_circ_147658,RMVar_hsa_circ_109567,RMVar_hsa_circ_326587,RMVar_hsa_circ_147659 4302 RMVar_ID_4302 Human_SNP_ID_453906959 A-to-I Human chr11 - 3701814 3701814 3701814 GGGCGTTGTGGCAGGCGCCTGTAGACCCAGCTAGTCAGGAGGCTGAGGCAGGAGAATGGTGTGAA GGGCGTTGTGGCAGGCGCCTGTAGACCCAGCTGGTCAGGAGGCTGAGGCAGGAGAATGGTGTGAA T C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs558175341 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75074,RMVar_hsa_circ_147634,RMVar_hsa_circ_367828,RMVar_hsa_circ_108806,RMVar_hsa_circ_106647,RMVar_hsa_circ_147635,RMVar_hsa_circ_75213,RMVar_hsa_circ_147638,RMVar_hsa_circ_35304,RMVar_hsa_circ_121348,RMVar_hsa_circ_125364,RMVar_hsa_circ_104783,RMVar_hsa_circ_147640,RMVar_hsa_circ_52316,RMVar_hsa_circ_147641,RMVar_hsa_circ_114245,RMVar_hsa_circ_147639,RMVar_hsa_circ_47819,RMVar_hsa_circ_147645,RMVar_hsa_circ_307900,RMVar_hsa_circ_321289,RMVar_hsa_circ_109406,RMVar_hsa_circ_97527,RMVar_hsa_circ_11860,RMVar_hsa_circ_37210,RMVar_hsa_circ_6580,RMVar_hsa_circ_9340,RMVar_hsa_circ_20849,RMVar_hsa_circ_71064,RMVar_hsa_circ_147651,RMVar_hsa_circ_147652,RMVar_hsa_circ_147650,RMVar_hsa_circ_349447,RMVar_hsa_circ_17317,RMVar_hsa_circ_374437,RMVar_hsa_circ_77589,RMVar_hsa_circ_51322,RMVar_hsa_circ_106281,RMVar_hsa_circ_147655,RMVar_hsa_circ_147654,RMVar_hsa_circ_361127,RMVar_hsa_circ_74486,RMVar_hsa_circ_147657,RMVar_hsa_circ_147658,RMVar_hsa_circ_109567,RMVar_hsa_circ_326587,RMVar_hsa_circ_147659 4303 RMVar_ID_4303 Human_SNP_ID_453907831 A-to-I Human chr11 - 3703963 3703963 3703963 TGTCCTTCAGCCGGGCACAGTGGCTCATGCCTATAATCATAGCACTTTAGGAGACTGAGGAAGGA TGTCCTTCAGCCGGGCACAGTGGCTCATGCCTGTAATCATAGCACTTTAGGAGACTGAGGAAGGA T C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1315909043 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6072449 RMVar_hsa_circ_75074,RMVar_hsa_circ_147634,RMVar_hsa_circ_367828,RMVar_hsa_circ_108806,RMVar_hsa_circ_106647,RMVar_hsa_circ_147635,RMVar_hsa_circ_35304,RMVar_hsa_circ_121348,RMVar_hsa_circ_125364,RMVar_hsa_circ_104783,RMVar_hsa_circ_147640,RMVar_hsa_circ_52316,RMVar_hsa_circ_147641,RMVar_hsa_circ_114245,RMVar_hsa_circ_147639,RMVar_hsa_circ_47819,RMVar_hsa_circ_147645,RMVar_hsa_circ_307900,RMVar_hsa_circ_109406,RMVar_hsa_circ_97527,RMVar_hsa_circ_11860,RMVar_hsa_circ_37210,RMVar_hsa_circ_6580,RMVar_hsa_circ_9340,RMVar_hsa_circ_20849,RMVar_hsa_circ_147651,RMVar_hsa_circ_147652,RMVar_hsa_circ_17317,RMVar_hsa_circ_374437,RMVar_hsa_circ_77589,RMVar_hsa_circ_51322,RMVar_hsa_circ_106281,RMVar_hsa_circ_147655,RMVar_hsa_circ_147654,RMVar_hsa_circ_74486,RMVar_hsa_circ_147661,RMVar_hsa_circ_119513,RMVar_hsa_circ_271689,RMVar_hsa_circ_147658,RMVar_hsa_circ_109567,RMVar_hsa_circ_362217,RMVar_hsa_circ_147659,RMVar_hsa_circ_359547,RMVar_hsa_circ_288748,RMVar_hsa_circ_125448,RMVar_hsa_circ_126192,RMVar_hsa_circ_123681,RMVar_hsa_circ_147665,RMVar_hsa_circ_147667,RMVar_hsa_circ_102009,RMVar_hsa_circ_147666,RMVar_hsa_circ_147663,RMVar_hsa_circ_147664,RMVar_hsa_circ_147662,RMVar_hsa_circ_51107,RMVar_hsa_circ_147660 4304 RMVar_ID_4304 Human_SNP_ID_453911635 A-to-I Human chr11 - 3718522 3718522 3718522 TTTCTTTCTTTCTTCTTTTGAGACAGAGTTTCACTCCTTTGCCCAAGCTGGAGTGCAGTGGTATA TTTCTTTCTTTCTTCTTTTGAGACAGAGTTTCGCTCCTTTGCCCAAGCTGGAGTGCAGTGGTATA T C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1392023477 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19696823 RMVar_hsa_circ_75074,RMVar_hsa_circ_147634,RMVar_hsa_circ_367828,RMVar_hsa_circ_108806,RMVar_hsa_circ_106647,RMVar_hsa_circ_147635,RMVar_hsa_circ_35304,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_47819,RMVar_hsa_circ_147645,RMVar_hsa_circ_307900,RMVar_hsa_circ_109406,RMVar_hsa_circ_97527,RMVar_hsa_circ_37210,RMVar_hsa_circ_6580,RMVar_hsa_circ_65551,RMVar_hsa_circ_20849,RMVar_hsa_circ_147651,RMVar_hsa_circ_147652,RMVar_hsa_circ_374437,RMVar_hsa_circ_77589,RMVar_hsa_circ_106281,RMVar_hsa_circ_147655,RMVar_hsa_circ_147654,RMVar_hsa_circ_74486,RMVar_hsa_circ_147661,RMVar_hsa_circ_119513,RMVar_hsa_circ_271689,RMVar_hsa_circ_147658,RMVar_hsa_circ_109567,RMVar_hsa_circ_362217,RMVar_hsa_circ_147659,RMVar_hsa_circ_125448,RMVar_hsa_circ_126192,RMVar_hsa_circ_123681,RMVar_hsa_circ_147665,RMVar_hsa_circ_102009,RMVar_hsa_circ_147666,RMVar_hsa_circ_147663,RMVar_hsa_circ_147664,RMVar_hsa_circ_147662,RMVar_hsa_circ_125545,RMVar_hsa_circ_147660,RMVar_hsa_circ_330940,RMVar_hsa_circ_375765,RMVar_hsa_circ_326676,RMVar_hsa_circ_128055,RMVar_hsa_circ_126244,RMVar_hsa_circ_95108,RMVar_hsa_circ_83167,RMVar_hsa_circ_42290,RMVar_hsa_circ_77363,RMVar_hsa_circ_147672,RMVar_hsa_circ_147676,RMVar_hsa_circ_29221,RMVar_hsa_circ_50353,RMVar_hsa_circ_147674,RMVar_hsa_circ_147675,RMVar_hsa_circ_147673,RMVar_hsa_circ_147670,RMVar_hsa_circ_147671,RMVar_hsa_circ_147669,RMVar_hsa_circ_67602,RMVar_hsa_circ_282660,RMVar_hsa_circ_147679,RMVar_hsa_circ_106002,RMVar_hsa_circ_44148,RMVar_hsa_circ_68815,RMVar_hsa_circ_74924,RMVar_hsa_circ_333214,RMVar_hsa_circ_345332,RMVar_hsa_circ_147680,RMVar_hsa_circ_335429,RMVar_hsa_circ_280832,RMVar_hsa_circ_147681,RMVar_hsa_circ_147682 4305 RMVar_ID_4305 Human_SNP_ID_453912563 A-to-I Human chr11 - 3721599 3721599 3721599 TGCCTCCCAGGTTCAAGCGATTCTCCTTCCTCAACCTCCCGAGTAGCTGGGATTACAAGCACCCG TGCCTCCCAGGTTCAAGCGATTCTCCTTCCTCCACCTCCCGAGTAGCTGGGATTACAAGCACCCG T G NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1472079834 Functional Loss SNV dbSNP153 33..33 33 - - - 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_109406,RMVar_hsa_circ_97527,RMVar_hsa_circ_37210,RMVar_hsa_circ_6580,RMVar_hsa_circ_20849,RMVar_hsa_circ_147651,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_126192,RMVar_hsa_circ_123681,RMVar_hsa_circ_147665,RMVar_hsa_circ_102009,RMVar_hsa_circ_147663,RMVar_hsa_circ_147664,RMVar_hsa_circ_147662,RMVar_hsa_circ_125545,RMVar_hsa_circ_147660,RMVar_hsa_circ_375765,RMVar_hsa_circ_326676,RMVar_hsa_circ_128055,RMVar_hsa_circ_126244,RMVar_hsa_circ_95108,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_147674,RMVar_hsa_circ_147675,RMVar_hsa_circ_147673,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_324665,RMVar_hsa_circ_363784,RMVar_hsa_circ_373076,RMVar_hsa_circ_285181,RMVar_hsa_circ_306532,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_147686 4306 RMVar_ID_4306 Human_SNP_ID_453912860 A-to-I Human chr11 - 3722704 3722703 3722704 GGATCAGGACCTCTCATCTCAGCCACCCGAGTAGCTGGCACTACAGGCACATGATACCACACCCC GGATCAGGACCTCTCATCTCAGCCACCCGAGT_GCTGGCACTACAGGCACATGATACCACACCCC CT C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1433878626 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_11613996 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_109406,RMVar_hsa_circ_97527,RMVar_hsa_circ_37210,RMVar_hsa_circ_6580,RMVar_hsa_circ_20849,RMVar_hsa_circ_147651,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_126192,RMVar_hsa_circ_123681,RMVar_hsa_circ_147665,RMVar_hsa_circ_102009,RMVar_hsa_circ_147663,RMVar_hsa_circ_147664,RMVar_hsa_circ_147662,RMVar_hsa_circ_125545,RMVar_hsa_circ_147660,RMVar_hsa_circ_375765,RMVar_hsa_circ_326676,RMVar_hsa_circ_128055,RMVar_hsa_circ_126244,RMVar_hsa_circ_95108,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_147674,RMVar_hsa_circ_147675,RMVar_hsa_circ_147673,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_324665,RMVar_hsa_circ_363784,RMVar_hsa_circ_373076,RMVar_hsa_circ_285181,RMVar_hsa_circ_306532,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_147686 4307 RMVar_ID_4307 Human_SNP_ID_453912864 A-to-I Human chr11 - 3722716 3722716 3722716 CTCAACCTCCAGGGATCAGGACCTCTCATCTCAGCCACCCGAGTAGCTGGCACTACAGGCACATG CTCAACCTCCAGGGATCAGGACCTCTCATCTCGGCCACCCGAGTAGCTGGCACTACAGGCACATG T C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1424209042 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6072544,Human_RBP_ID_11613997 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_109406,RMVar_hsa_circ_97527,RMVar_hsa_circ_37210,RMVar_hsa_circ_6580,RMVar_hsa_circ_20849,RMVar_hsa_circ_147651,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_126192,RMVar_hsa_circ_123681,RMVar_hsa_circ_147665,RMVar_hsa_circ_102009,RMVar_hsa_circ_147663,RMVar_hsa_circ_147664,RMVar_hsa_circ_147662,RMVar_hsa_circ_125545,RMVar_hsa_circ_147660,RMVar_hsa_circ_375765,RMVar_hsa_circ_326676,RMVar_hsa_circ_128055,RMVar_hsa_circ_126244,RMVar_hsa_circ_95108,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_147674,RMVar_hsa_circ_147675,RMVar_hsa_circ_147673,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_324665,RMVar_hsa_circ_363784,RMVar_hsa_circ_373076,RMVar_hsa_circ_285181,RMVar_hsa_circ_306532,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_147686 4308 RMVar_ID_4308 Human_SNP_ID_453914490 A-to-I Human chr11 - 3727971 3727971 3727971 TGTCACCCAGGCTGGAGTGCGGTGGCGCTGTCATAGCTCACTGCACCCTTGAATTCCTGGGCTCG TGTCACCCAGGCTGGAGTGCGGTGGCGCTGTCGTAGCTCACTGCACCCTTGAATTCCTGGGCTCG T C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs559426202 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11614084 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_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_102009,RMVar_hsa_circ_147663,RMVar_hsa_circ_147664,RMVar_hsa_circ_147662,RMVar_hsa_circ_125545,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_147673,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_306532,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_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_306895,RMVar_hsa_circ_147694,RMVar_hsa_circ_147696,RMVar_hsa_circ_67580,RMVar_hsa_circ_147695,RMVar_hsa_circ_147693 4309 RMVar_ID_4309 Human_SNP_ID_453917571 A-to-I Human chr11 - 3738494 3738494 3738494 GATTACTGGCATGAGCCACCATGCCTTGCTGTAGTATATTTGTGGTAACCCACTGACTTTCTTCT GATTACTGGCATGAGCCACCATGCCTTGCTGTGGTATATTTGTGGTAACCCACTGACTTTCTTCT T C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1211691739 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11614275 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_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_106002,RMVar_hsa_circ_44148,RMVar_hsa_circ_67070,RMVar_hsa_circ_68815,RMVar_hsa_circ_345332,RMVar_hsa_circ_147680,RMVar_hsa_circ_335429,RMVar_hsa_circ_306864,RMVar_hsa_circ_147681,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_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_374371,RMVar_hsa_circ_272250,RMVar_hsa_circ_147694,RMVar_hsa_circ_67580,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_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 4310 RMVar_ID_4310 Human_SNP_ID_453917581 A-to-I Human chr11 - 3738535 3738535 3738535 GACCTGAAGTAATCTGCTTGCTCAGCTTCCCAAAGTGCTGGGATTACTGGCATGAGCCACCATGC GACCTGAAGTAATCTGCTTGCTCAGCTTCCCAGAGTGCTGGGATTACTGGCATGAGCCACCATGC T C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1055341878 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8351190 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_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_106002,RMVar_hsa_circ_44148,RMVar_hsa_circ_67070,RMVar_hsa_circ_68815,RMVar_hsa_circ_345332,RMVar_hsa_circ_147680,RMVar_hsa_circ_335429,RMVar_hsa_circ_306864,RMVar_hsa_circ_147681,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_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_374371,RMVar_hsa_circ_272250,RMVar_hsa_circ_147694,RMVar_hsa_circ_67580,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_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 4311 RMVar_ID_4311 Human_SNP_ID_453917582 A-to-I Human chr11 - 3738544 3738544 3738544 TGAAGTCCTGACCTGAAGTAATCTGCTTGCTCAGCTTCCCAAAGTGCTGGGATTACTGGCATGAG TGAAGTCCTGACCTGAAGTAATCTGCTTGCTCTGCTTCCCAAAGTGCTGGGATTACTGGCATGAG T A NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1398125477 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8351190 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_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_106002,RMVar_hsa_circ_44148,RMVar_hsa_circ_67070,RMVar_hsa_circ_68815,RMVar_hsa_circ_345332,RMVar_hsa_circ_147680,RMVar_hsa_circ_335429,RMVar_hsa_circ_306864,RMVar_hsa_circ_147681,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_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_374371,RMVar_hsa_circ_272250,RMVar_hsa_circ_147694,RMVar_hsa_circ_67580,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_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 4312 RMVar_ID_4312 Human_SNP_ID_453917590 A-to-I Human chr11 - 3738581 3738581 3738581 TAGAGATAGAGGTTCACCATTTTGGCCAGGCTATTCTTGAAGTCCTGACCTGAAGTAATCTGCTT TAGAGATAGAGGTTCACCATTTTGGCCAGGCTGTTCTTGAAGTCCTGACCTGAAGTAATCTGCTT T C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs751124143 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11614279 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_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_106002,RMVar_hsa_circ_44148,RMVar_hsa_circ_67070,RMVar_hsa_circ_68815,RMVar_hsa_circ_345332,RMVar_hsa_circ_147680,RMVar_hsa_circ_335429,RMVar_hsa_circ_306864,RMVar_hsa_circ_147681,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_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_374371,RMVar_hsa_circ_272250,RMVar_hsa_circ_147694,RMVar_hsa_circ_67580,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_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 4313 RMVar_ID_4313 Human_SNP_ID_453917591 A-to-I Human chr11 - 3738581 3738581 3738581 TAGAGATAGAGGTTCACCATTTTGGCCAGGCTATTCTTGAAGTCCTGACCTGAAGTAATCTGCTT TAGAGATAGAGGTTCACCATTTTGGCCAGGCTCTTCTTGAAGTCCTGACCTGAAGTAATCTGCTT T G NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs751124143 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11614279 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_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_106002,RMVar_hsa_circ_44148,RMVar_hsa_circ_67070,RMVar_hsa_circ_68815,RMVar_hsa_circ_345332,RMVar_hsa_circ_147680,RMVar_hsa_circ_335429,RMVar_hsa_circ_306864,RMVar_hsa_circ_147681,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_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_374371,RMVar_hsa_circ_272250,RMVar_hsa_circ_147694,RMVar_hsa_circ_67580,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_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 4314 RMVar_ID_4314 Human_SNP_ID_453917610 A-to-I Human chr11 - 3738667 3738667 3738667 TCAGACAATTCTCCTGTCTCAGCCTCCTGCGTAGCTGGGACTACAGGTATGTGTCACCATGCCCG TCAGACAATTCTCCTGTCTCAGCCTCCTGCGTGGCTGGGACTACAGGTATGTGTCACCATGCCCG T C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1230882303 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_106002,RMVar_hsa_circ_44148,RMVar_hsa_circ_67070,RMVar_hsa_circ_68815,RMVar_hsa_circ_345332,RMVar_hsa_circ_147680,RMVar_hsa_circ_335429,RMVar_hsa_circ_306864,RMVar_hsa_circ_147681,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_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_374371,RMVar_hsa_circ_272250,RMVar_hsa_circ_147694,RMVar_hsa_circ_67580,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_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 4315 RMVar_ID_4315 Human_SNP_ID_453918120 A-to-I Human chr11 - 3740289 3740289 3740289 CTAGGCTGGTCACGAACTCCTGACCTCAAGCAATCCTCTCGCTTCGGCCTCCCAAAGTGCTGGGG CTAGGCTGGTCACGAACTCCTGACCTCAAGCAGTCCTCTCGCTTCGGCCTCCCAAAGTGCTGGGG T C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1245590428 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_106002,RMVar_hsa_circ_44148,RMVar_hsa_circ_67070,RMVar_hsa_circ_68815,RMVar_hsa_circ_345332,RMVar_hsa_circ_147680,RMVar_hsa_circ_335429,RMVar_hsa_circ_306864,RMVar_hsa_circ_147681,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_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_374371,RMVar_hsa_circ_272250,RMVar_hsa_circ_147694,RMVar_hsa_circ_67580,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_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 4316 RMVar_ID_4316 Human_SNP_ID_453918132 A-to-I Human chr11 - 3740326 3740326 3740326 TTGTATTTTTAGTAGGTATTGGGTTTCACCATATTGGCTAGGCTGGTCACGAACTCCTGACCTCA TTGTATTTTTAGTAGGTATTGGGTTTCACCATGTTGGCTAGGCTGGTCACGAACTCCTGACCTCA T C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs111526141 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11614309,Human_RBP_ID_24884447 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_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_106002,RMVar_hsa_circ_44148,RMVar_hsa_circ_67070,RMVar_hsa_circ_68815,RMVar_hsa_circ_345332,RMVar_hsa_circ_147680,RMVar_hsa_circ_335429,RMVar_hsa_circ_306864,RMVar_hsa_circ_147681,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_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_374371,RMVar_hsa_circ_272250,RMVar_hsa_circ_147694,RMVar_hsa_circ_67580,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_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 4317 RMVar_ID_4317 Human_SNP_ID_453918163 A-to-I Human chr11 - 3740435 3740435 3740435 TTGATCTTGGCTCACTGCAACCTTCGCCTCCCAGGTTCAAGTGATTCTCTTTCCTCAGCCTCTTG TTGATCTTGGCTCACTGCAACCTTCGCCTCCCGGGTTCAAGTGATTCTCTTTCCTCAGCCTCTTG T C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1345752012 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_106002,RMVar_hsa_circ_44148,RMVar_hsa_circ_67070,RMVar_hsa_circ_68815,RMVar_hsa_circ_345332,RMVar_hsa_circ_147680,RMVar_hsa_circ_335429,RMVar_hsa_circ_306864,RMVar_hsa_circ_147681,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_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_374371,RMVar_hsa_circ_272250,RMVar_hsa_circ_147694,RMVar_hsa_circ_67580,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_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 4318 RMVar_ID_4318 Human_SNP_ID_453918168 A-to-I Human chr11 - 3740448 3740448 3740448 TAGTGGTGTGATCTTGATCTTGGCTCACTGCAACCTTCGCCTCCCAGGTTCAAGTGATTCTCTTT TAGTGGTGTGATCTTGATCTTGGCTCACTGCAGCCTTCGCCTCCCAGGTTCAAGTGATTCTCTTT T C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs543481655 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_106002,RMVar_hsa_circ_44148,RMVar_hsa_circ_67070,RMVar_hsa_circ_68815,RMVar_hsa_circ_345332,RMVar_hsa_circ_147680,RMVar_hsa_circ_335429,RMVar_hsa_circ_306864,RMVar_hsa_circ_147681,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_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_374371,RMVar_hsa_circ_272250,RMVar_hsa_circ_147694,RMVar_hsa_circ_67580,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_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 4319 RMVar_ID_4319 Human_SNP_ID_453918375 A-to-I Human chr11 - 3741048 3741048 3741048 GGAGGCTGAGGCAGGCGGATTGCTTGAGGTCAAGCGTTCGAGACCAGCCTGGCCAACATGGCAAA GGAGGCTGAGGCAGGCGGATTGCTTGAGGTCACGCGTTCGAGACCAGCCTGGCCAACATGGCAAA T G NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1009341646 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_106002,RMVar_hsa_circ_44148,RMVar_hsa_circ_67070,RMVar_hsa_circ_68815,RMVar_hsa_circ_345332,RMVar_hsa_circ_147680,RMVar_hsa_circ_335429,RMVar_hsa_circ_306864,RMVar_hsa_circ_147681,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_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_374371,RMVar_hsa_circ_272250,RMVar_hsa_circ_147694,RMVar_hsa_circ_67580,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_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 4320 RMVar_ID_4320 Human_SNP_ID_453918781 A-to-I Human chr11 - 3742599 3742599 3742599 TGCCTCCCAGGTTCAAGCAATTCTGCTGCCTCAGCTTCCTGAGTAGCTGGGATTACAGGTGCCTG TGCCTCCCAGGTTCAAGCAATTCTGCTGCCTCTGCTTCCTGAGTAGCTGGGATTACAGGTGCCTG T A NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1220562399 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24884466 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_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_106002,RMVar_hsa_circ_44148,RMVar_hsa_circ_67070,RMVar_hsa_circ_68815,RMVar_hsa_circ_345332,RMVar_hsa_circ_147680,RMVar_hsa_circ_335429,RMVar_hsa_circ_306864,RMVar_hsa_circ_147681,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_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_374371,RMVar_hsa_circ_272250,RMVar_hsa_circ_147694,RMVar_hsa_circ_67580,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_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 4321 RMVar_ID_4321 Human_SNP_ID_453918980 A-to-I Human chr11 - 3743143 3743143 3743143 ATGATGGCATGTGCATGTAATCCTAGGTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGGACCCG ATGATGGCATGTGCATGTAATCCTAGGTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGGACCCG T C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1371290931 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_106002,RMVar_hsa_circ_44148,RMVar_hsa_circ_67070,RMVar_hsa_circ_68815,RMVar_hsa_circ_345332,RMVar_hsa_circ_147680,RMVar_hsa_circ_335429,RMVar_hsa_circ_306864,RMVar_hsa_circ_147681,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_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_374371,RMVar_hsa_circ_272250,RMVar_hsa_circ_147694,RMVar_hsa_circ_67580,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_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 4322 RMVar_ID_4322 Human_SNP_ID_453918999 A-to-I Human chr11 - 3743198 3743198 3743198 CCTGGCCAACACGGTGAAACCCCATCTCTATTAAAAATGCAAAAATTAGCTGGGCATGATGGCAT CCTGGCCAACACGGTGAAACCCCATCTCTATTTAAAATGCAAAAATTAGCTGGGCATGATGGCAT T A NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs938720959 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_106002,RMVar_hsa_circ_44148,RMVar_hsa_circ_67070,RMVar_hsa_circ_68815,RMVar_hsa_circ_345332,RMVar_hsa_circ_147680,RMVar_hsa_circ_335429,RMVar_hsa_circ_306864,RMVar_hsa_circ_147681,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_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_374371,RMVar_hsa_circ_272250,RMVar_hsa_circ_147694,RMVar_hsa_circ_67580,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_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 4323 RMVar_ID_4323 Human_SNP_ID_453919025 A-to-I Human chr11 - 3743292 3743292 3743292 AAATTATGGGCTGGACCTGGTGGCCCACGCCTATAATCCCAGTACTTTGGGAGGCCGAGGCGGGT AAATTATGGGCTGGACCTGGTGGCCCACGCCTGTAATCCCAGTACTTTGGGAGGCCGAGGCGGGT T C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs536873071 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_106002,RMVar_hsa_circ_44148,RMVar_hsa_circ_67070,RMVar_hsa_circ_68815,RMVar_hsa_circ_345332,RMVar_hsa_circ_147680,RMVar_hsa_circ_335429,RMVar_hsa_circ_306864,RMVar_hsa_circ_147681,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_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_374371,RMVar_hsa_circ_272250,RMVar_hsa_circ_147694,RMVar_hsa_circ_67580,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_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 4324 RMVar_ID_4324 Human_SNP_ID_453920119 A-to-I Human chr11 - 3746830 3746830 3746830 CGGCTCACTGCAACCTCCGCCTCCCGGGCTCAAGCGATTCTCCTGCTTCAGCCTTCCCGAGTAGC CGGCTCACTGCAACCTCCGCCTCCCGGGCTCAGGCGATTCTCCTGCTTCAGCCTTCCCGAGTAGC T C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs948257403 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_271689,RMVar_hsa_circ_147658,RMVar_hsa_circ_109567,RMVar_hsa_circ_147659,RMVar_hsa_circ_125448,RMVar_hsa_circ_123681,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_147672,RMVar_hsa_circ_50353,RMVar_hsa_circ_147670,RMVar_hsa_circ_147671,RMVar_hsa_circ_147669,RMVar_hsa_circ_67602,RMVar_hsa_circ_106002,RMVar_hsa_circ_67070,RMVar_hsa_circ_68815,RMVar_hsa_circ_345332,RMVar_hsa_circ_147680,RMVar_hsa_circ_306864,RMVar_hsa_circ_373076,RMVar_hsa_circ_120713,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_147686,RMVar_hsa_circ_276230,RMVar_hsa_circ_101156,RMVar_hsa_circ_65040,RMVar_hsa_circ_92246,RMVar_hsa_circ_117554,RMVar_hsa_circ_147690,RMVar_hsa_circ_147691,RMVar_hsa_circ_147692,RMVar_hsa_circ_147689,RMVar_hsa_circ_374371,RMVar_hsa_circ_272250,RMVar_hsa_circ_147694,RMVar_hsa_circ_372984,RMVar_hsa_circ_147693,RMVar_hsa_circ_357330,RMVar_hsa_circ_97199,RMVar_hsa_circ_95967,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_101460,RMVar_hsa_circ_301735,RMVar_hsa_circ_273538,RMVar_hsa_circ_91945,RMVar_hsa_circ_78263,RMVar_hsa_circ_147709,RMVar_hsa_circ_147710,RMVar_hsa_circ_147708,RMVar_hsa_circ_287471,RMVar_hsa_circ_147711,RMVar_hsa_circ_147712 4325 RMVar_ID_4325 Human_SNP_ID_453921140 A-to-I Human chr11 - 3750363 3750363 3750363 AGCTGGATGAGGTGGCTCATGCCTGTAATGCCAGGTCTTTGGGAGGCTGAGGTGGGCGGATTACT AGCTGGATGAGGTGGCTCATGCCTGTAATGCCCGGTCTTTGGGAGGCTGAGGTGGGCGGATTACT T G NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749745714 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11614599 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_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_271689,RMVar_hsa_circ_147658,RMVar_hsa_circ_109567,RMVar_hsa_circ_147659,RMVar_hsa_circ_125448,RMVar_hsa_circ_123681,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_147672,RMVar_hsa_circ_50353,RMVar_hsa_circ_147670,RMVar_hsa_circ_147671,RMVar_hsa_circ_147669,RMVar_hsa_circ_67602,RMVar_hsa_circ_106002,RMVar_hsa_circ_67070,RMVar_hsa_circ_68815,RMVar_hsa_circ_345332,RMVar_hsa_circ_147680,RMVar_hsa_circ_306864,RMVar_hsa_circ_373076,RMVar_hsa_circ_120713,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_147686,RMVar_hsa_circ_276230,RMVar_hsa_circ_101156,RMVar_hsa_circ_65040,RMVar_hsa_circ_92246,RMVar_hsa_circ_117554,RMVar_hsa_circ_147690,RMVar_hsa_circ_147691,RMVar_hsa_circ_147692,RMVar_hsa_circ_147689,RMVar_hsa_circ_374371,RMVar_hsa_circ_272250,RMVar_hsa_circ_147694,RMVar_hsa_circ_372984,RMVar_hsa_circ_147693,RMVar_hsa_circ_357330,RMVar_hsa_circ_97199,RMVar_hsa_circ_95967,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_101460,RMVar_hsa_circ_301735,RMVar_hsa_circ_273538,RMVar_hsa_circ_91945,RMVar_hsa_circ_78263,RMVar_hsa_circ_147709,RMVar_hsa_circ_147710,RMVar_hsa_circ_147708,RMVar_hsa_circ_287471,RMVar_hsa_circ_147711,RMVar_hsa_circ_147712 4326 RMVar_ID_4326 Human_SNP_ID_453921518 A-to-I Human chr11 - 3751796 3751796 3751796 GGAGTGCATTGGCATGATCACAGCTCACTGCAACCTCTACCTCCCAGGCTCAAACCATCCTCCCA GGAGTGCATTGGCATGATCACAGCTCACTGCAGCCTCTACCTCCCAGGCTCAAACCATCCTCCCA T C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1296713811 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_271689,RMVar_hsa_circ_147658,RMVar_hsa_circ_109567,RMVar_hsa_circ_147659,RMVar_hsa_circ_125448,RMVar_hsa_circ_123681,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_147672,RMVar_hsa_circ_50353,RMVar_hsa_circ_147670,RMVar_hsa_circ_147671,RMVar_hsa_circ_147669,RMVar_hsa_circ_67602,RMVar_hsa_circ_106002,RMVar_hsa_circ_67070,RMVar_hsa_circ_68815,RMVar_hsa_circ_345332,RMVar_hsa_circ_147680,RMVar_hsa_circ_306864,RMVar_hsa_circ_373076,RMVar_hsa_circ_120713,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_147686,RMVar_hsa_circ_276230,RMVar_hsa_circ_101156,RMVar_hsa_circ_65040,RMVar_hsa_circ_92246,RMVar_hsa_circ_117554,RMVar_hsa_circ_147690,RMVar_hsa_circ_147691,RMVar_hsa_circ_147692,RMVar_hsa_circ_147689,RMVar_hsa_circ_374371,RMVar_hsa_circ_272250,RMVar_hsa_circ_147694,RMVar_hsa_circ_372984,RMVar_hsa_circ_147693,RMVar_hsa_circ_357330,RMVar_hsa_circ_97199,RMVar_hsa_circ_95967,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_101460,RMVar_hsa_circ_301735,RMVar_hsa_circ_273538,RMVar_hsa_circ_91945,RMVar_hsa_circ_78263,RMVar_hsa_circ_147709,RMVar_hsa_circ_147710,RMVar_hsa_circ_147708,RMVar_hsa_circ_287471,RMVar_hsa_circ_147711,RMVar_hsa_circ_147712 4327 RMVar_ID_4327 Human_SNP_ID_453922475 A-to-I Human chr11 - 3754855 3754855 3754855 TTACTGCAGCCTCTGCCTCCCGGGTTTAAGCAATTCTCCTGCTTCAGCCTCCCAAGTGGTTGGGA TTACTGCAGCCTCTGCCTCCCGGGTTTAAGCAGTTCTCCTGCTTCAGCCTCCCAAGTGGTTGGGA T C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1258187185 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11614788 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_97527,RMVar_hsa_circ_37210,RMVar_hsa_circ_38524,RMVar_hsa_circ_12367,RMVar_hsa_circ_147652,RMVar_hsa_circ_77589,RMVar_hsa_circ_106281,RMVar_hsa_circ_147654,RMVar_hsa_circ_147661,RMVar_hsa_circ_147658,RMVar_hsa_circ_109567,RMVar_hsa_circ_147659,RMVar_hsa_circ_125448,RMVar_hsa_circ_123681,RMVar_hsa_circ_147660,RMVar_hsa_circ_128055,RMVar_hsa_circ_126244,RMVar_hsa_circ_83167,RMVar_hsa_circ_50353,RMVar_hsa_circ_147670,RMVar_hsa_circ_147671,RMVar_hsa_circ_147669,RMVar_hsa_circ_106002,RMVar_hsa_circ_67070,RMVar_hsa_circ_68815,RMVar_hsa_circ_147680,RMVar_hsa_circ_373076,RMVar_hsa_circ_120713,RMVar_hsa_circ_147684,RMVar_hsa_circ_147685,RMVar_hsa_circ_85220,RMVar_hsa_circ_84143,RMVar_hsa_circ_121259,RMVar_hsa_circ_147686,RMVar_hsa_circ_101156,RMVar_hsa_circ_65040,RMVar_hsa_circ_92246,RMVar_hsa_circ_117554,RMVar_hsa_circ_147690,RMVar_hsa_circ_147691,RMVar_hsa_circ_147692,RMVar_hsa_circ_374371,RMVar_hsa_circ_147694,RMVar_hsa_circ_372984,RMVar_hsa_circ_147693,RMVar_hsa_circ_357330,RMVar_hsa_circ_97199,RMVar_hsa_circ_95967,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_147701,RMVar_hsa_circ_101460,RMVar_hsa_circ_301735,RMVar_hsa_circ_91945,RMVar_hsa_circ_147713,RMVar_hsa_circ_78263,RMVar_hsa_circ_147709,RMVar_hsa_circ_147708,RMVar_hsa_circ_333940,RMVar_hsa_circ_147712,RMVar_hsa_circ_348744,RMVar_hsa_circ_373682,RMVar_hsa_circ_346114,RMVar_hsa_circ_68884,RMVar_hsa_circ_114985,RMVar_hsa_circ_147714 4328 RMVar_ID_4328 Human_SNP_ID_453922731 A-to-I Human chr11 - 3755711 3755711 3755711 ATCCACCTGCCTTGGCCTCCCAAAGTGGCGGGATTACAGGCGTGAGCCACTGCGCCCGGCCTGCT ATCCACCTGCCTTGGCCTCCCAAAGTGGCGGGGTTACAGGCGTGAGCCACTGCGCCCGGCCTGCT T C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978891067 Functional Loss SNV dbSNP153 33..33 33 - - - 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_97527,RMVar_hsa_circ_37210,RMVar_hsa_circ_38524,RMVar_hsa_circ_12367,RMVar_hsa_circ_147652,RMVar_hsa_circ_77589,RMVar_hsa_circ_106281,RMVar_hsa_circ_147654,RMVar_hsa_circ_147661,RMVar_hsa_circ_147658,RMVar_hsa_circ_109567,RMVar_hsa_circ_147659,RMVar_hsa_circ_125448,RMVar_hsa_circ_123681,RMVar_hsa_circ_147660,RMVar_hsa_circ_128055,RMVar_hsa_circ_126244,RMVar_hsa_circ_83167,RMVar_hsa_circ_50353,RMVar_hsa_circ_147670,RMVar_hsa_circ_147671,RMVar_hsa_circ_147669,RMVar_hsa_circ_106002,RMVar_hsa_circ_67070,RMVar_hsa_circ_68815,RMVar_hsa_circ_147680,RMVar_hsa_circ_373076,RMVar_hsa_circ_120713,RMVar_hsa_circ_147684,RMVar_hsa_circ_147685,RMVar_hsa_circ_85220,RMVar_hsa_circ_84143,RMVar_hsa_circ_121259,RMVar_hsa_circ_147686,RMVar_hsa_circ_101156,RMVar_hsa_circ_65040,RMVar_hsa_circ_92246,RMVar_hsa_circ_117554,RMVar_hsa_circ_147690,RMVar_hsa_circ_147691,RMVar_hsa_circ_147692,RMVar_hsa_circ_374371,RMVar_hsa_circ_147694,RMVar_hsa_circ_372984,RMVar_hsa_circ_147693,RMVar_hsa_circ_357330,RMVar_hsa_circ_97199,RMVar_hsa_circ_95967,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_147701,RMVar_hsa_circ_101460,RMVar_hsa_circ_301735,RMVar_hsa_circ_91945,RMVar_hsa_circ_147713,RMVar_hsa_circ_78263,RMVar_hsa_circ_147709,RMVar_hsa_circ_147708,RMVar_hsa_circ_333940,RMVar_hsa_circ_147712,RMVar_hsa_circ_348744,RMVar_hsa_circ_373682,RMVar_hsa_circ_346114,RMVar_hsa_circ_68884,RMVar_hsa_circ_114985,RMVar_hsa_circ_147714 4329 RMVar_ID_4329 Human_SNP_ID_453922941 A-to-I Human chr11 - 3756525 3756525 3756525 CCAGCTACTCGGGAGGCTGAGGCAGAAGAATCACTTGAACCCAGGAGGCAGAAGTTGCAGTGATG CCAGCTACTCGGGAGGCTGAGGCAGAAGAATCGCTTGAACCCAGGAGGCAGAAGTTGCAGTGATG T C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947550201 Functional Loss SNV dbSNP153 33..33 33 - - - 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_97527,RMVar_hsa_circ_37210,RMVar_hsa_circ_38524,RMVar_hsa_circ_12367,RMVar_hsa_circ_147652,RMVar_hsa_circ_77589,RMVar_hsa_circ_106281,RMVar_hsa_circ_147654,RMVar_hsa_circ_147661,RMVar_hsa_circ_147658,RMVar_hsa_circ_109567,RMVar_hsa_circ_147659,RMVar_hsa_circ_125448,RMVar_hsa_circ_123681,RMVar_hsa_circ_147660,RMVar_hsa_circ_128055,RMVar_hsa_circ_126244,RMVar_hsa_circ_83167,RMVar_hsa_circ_50353,RMVar_hsa_circ_147670,RMVar_hsa_circ_147671,RMVar_hsa_circ_147669,RMVar_hsa_circ_106002,RMVar_hsa_circ_67070,RMVar_hsa_circ_68815,RMVar_hsa_circ_147680,RMVar_hsa_circ_373076,RMVar_hsa_circ_120713,RMVar_hsa_circ_147684,RMVar_hsa_circ_147685,RMVar_hsa_circ_85220,RMVar_hsa_circ_84143,RMVar_hsa_circ_121259,RMVar_hsa_circ_147686,RMVar_hsa_circ_101156,RMVar_hsa_circ_65040,RMVar_hsa_circ_92246,RMVar_hsa_circ_117554,RMVar_hsa_circ_147690,RMVar_hsa_circ_147691,RMVar_hsa_circ_147692,RMVar_hsa_circ_374371,RMVar_hsa_circ_147694,RMVar_hsa_circ_372984,RMVar_hsa_circ_147693,RMVar_hsa_circ_357330,RMVar_hsa_circ_97199,RMVar_hsa_circ_95967,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_147701,RMVar_hsa_circ_101460,RMVar_hsa_circ_301735,RMVar_hsa_circ_91945,RMVar_hsa_circ_147713,RMVar_hsa_circ_78263,RMVar_hsa_circ_147709,RMVar_hsa_circ_147708,RMVar_hsa_circ_333940,RMVar_hsa_circ_147712,RMVar_hsa_circ_348744,RMVar_hsa_circ_373682,RMVar_hsa_circ_346114,RMVar_hsa_circ_68884,RMVar_hsa_circ_114985,RMVar_hsa_circ_147714 4330 RMVar_ID_4330 Human_SNP_ID_453922971 A-to-I Human chr11 - 3756611 3756611 3756611 TCGAGATAGACTGGCCAGCATGGTAAAACCCCATTTCTACTAAAAACACAAAAATTAGCTGGGCA TCGAGATAGACTGGCCAGCATGGTAAAACCCCGTTTCTACTAAAAACACAAAAATTAGCTGGGCA T C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1461043695 Functional Loss SNV dbSNP153 33..33 33 - - - 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_97527,RMVar_hsa_circ_37210,RMVar_hsa_circ_38524,RMVar_hsa_circ_12367,RMVar_hsa_circ_147652,RMVar_hsa_circ_77589,RMVar_hsa_circ_106281,RMVar_hsa_circ_147654,RMVar_hsa_circ_147661,RMVar_hsa_circ_147658,RMVar_hsa_circ_109567,RMVar_hsa_circ_147659,RMVar_hsa_circ_125448,RMVar_hsa_circ_123681,RMVar_hsa_circ_147660,RMVar_hsa_circ_128055,RMVar_hsa_circ_126244,RMVar_hsa_circ_83167,RMVar_hsa_circ_50353,RMVar_hsa_circ_147670,RMVar_hsa_circ_147671,RMVar_hsa_circ_147669,RMVar_hsa_circ_106002,RMVar_hsa_circ_67070,RMVar_hsa_circ_68815,RMVar_hsa_circ_147680,RMVar_hsa_circ_373076,RMVar_hsa_circ_120713,RMVar_hsa_circ_147684,RMVar_hsa_circ_147685,RMVar_hsa_circ_85220,RMVar_hsa_circ_84143,RMVar_hsa_circ_121259,RMVar_hsa_circ_147686,RMVar_hsa_circ_101156,RMVar_hsa_circ_65040,RMVar_hsa_circ_92246,RMVar_hsa_circ_117554,RMVar_hsa_circ_147690,RMVar_hsa_circ_147691,RMVar_hsa_circ_147692,RMVar_hsa_circ_374371,RMVar_hsa_circ_147694,RMVar_hsa_circ_372984,RMVar_hsa_circ_147693,RMVar_hsa_circ_357330,RMVar_hsa_circ_97199,RMVar_hsa_circ_95967,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_147701,RMVar_hsa_circ_101460,RMVar_hsa_circ_301735,RMVar_hsa_circ_91945,RMVar_hsa_circ_147713,RMVar_hsa_circ_78263,RMVar_hsa_circ_147709,RMVar_hsa_circ_147708,RMVar_hsa_circ_333940,RMVar_hsa_circ_147712,RMVar_hsa_circ_348744,RMVar_hsa_circ_373682,RMVar_hsa_circ_346114,RMVar_hsa_circ_68884,RMVar_hsa_circ_114985,RMVar_hsa_circ_147714 4331 RMVar_ID_4331 Human_SNP_ID_453923039 A-to-I Human chr11 - 3756844 3756844 3756844 TGACCTCGTGATCCGCTCACCTCGGCCTCCCAAAAGGTTGGGATTACAGGCGTGAGCCACTGCGC TGACCTCGTGATCCGCTCACCTCGGCCTCCCAGAAGGTTGGGATTACAGGCGTGAGCCACTGCGC T C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs549281440 Functional Loss SNV dbSNP153 33..33 33 - - - 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_97527,RMVar_hsa_circ_37210,RMVar_hsa_circ_38524,RMVar_hsa_circ_12367,RMVar_hsa_circ_147652,RMVar_hsa_circ_77589,RMVar_hsa_circ_106281,RMVar_hsa_circ_147654,RMVar_hsa_circ_147661,RMVar_hsa_circ_147658,RMVar_hsa_circ_109567,RMVar_hsa_circ_147659,RMVar_hsa_circ_125448,RMVar_hsa_circ_123681,RMVar_hsa_circ_147660,RMVar_hsa_circ_128055,RMVar_hsa_circ_126244,RMVar_hsa_circ_83167,RMVar_hsa_circ_50353,RMVar_hsa_circ_147670,RMVar_hsa_circ_147671,RMVar_hsa_circ_147669,RMVar_hsa_circ_106002,RMVar_hsa_circ_67070,RMVar_hsa_circ_68815,RMVar_hsa_circ_147680,RMVar_hsa_circ_373076,RMVar_hsa_circ_120713,RMVar_hsa_circ_147684,RMVar_hsa_circ_147685,RMVar_hsa_circ_85220,RMVar_hsa_circ_84143,RMVar_hsa_circ_121259,RMVar_hsa_circ_147686,RMVar_hsa_circ_101156,RMVar_hsa_circ_65040,RMVar_hsa_circ_92246,RMVar_hsa_circ_117554,RMVar_hsa_circ_147690,RMVar_hsa_circ_147691,RMVar_hsa_circ_147692,RMVar_hsa_circ_374371,RMVar_hsa_circ_147694,RMVar_hsa_circ_372984,RMVar_hsa_circ_147693,RMVar_hsa_circ_357330,RMVar_hsa_circ_97199,RMVar_hsa_circ_95967,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_147701,RMVar_hsa_circ_101460,RMVar_hsa_circ_301735,RMVar_hsa_circ_91945,RMVar_hsa_circ_147713,RMVar_hsa_circ_78263,RMVar_hsa_circ_147709,RMVar_hsa_circ_147708,RMVar_hsa_circ_333940,RMVar_hsa_circ_147712,RMVar_hsa_circ_348744,RMVar_hsa_circ_373682,RMVar_hsa_circ_346114,RMVar_hsa_circ_68884,RMVar_hsa_circ_114985,RMVar_hsa_circ_147714 4332 RMVar_ID_4332 Human_SNP_ID_453923072 A-to-I Human chr11 - 3756923 3756923 3756923 CTGCCACGTCTGGCTAATTTTTTTGTATTCTTAATAGAGACGGGGTTTCACCATGTTAGCCGGGA CTGCCACGTCTGGCTAATTTTTTTGTATTCTTTATAGAGACGGGGTTTCACCATGTTAGCCGGGA T A NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886931349 Functional Loss SNV dbSNP153 33..33 33 - - - 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_97527,RMVar_hsa_circ_37210,RMVar_hsa_circ_38524,RMVar_hsa_circ_12367,RMVar_hsa_circ_147652,RMVar_hsa_circ_77589,RMVar_hsa_circ_106281,RMVar_hsa_circ_147654,RMVar_hsa_circ_147661,RMVar_hsa_circ_147658,RMVar_hsa_circ_109567,RMVar_hsa_circ_147659,RMVar_hsa_circ_125448,RMVar_hsa_circ_123681,RMVar_hsa_circ_147660,RMVar_hsa_circ_128055,RMVar_hsa_circ_126244,RMVar_hsa_circ_83167,RMVar_hsa_circ_50353,RMVar_hsa_circ_147670,RMVar_hsa_circ_147671,RMVar_hsa_circ_147669,RMVar_hsa_circ_106002,RMVar_hsa_circ_67070,RMVar_hsa_circ_68815,RMVar_hsa_circ_147680,RMVar_hsa_circ_373076,RMVar_hsa_circ_120713,RMVar_hsa_circ_147684,RMVar_hsa_circ_147685,RMVar_hsa_circ_85220,RMVar_hsa_circ_84143,RMVar_hsa_circ_121259,RMVar_hsa_circ_147686,RMVar_hsa_circ_101156,RMVar_hsa_circ_65040,RMVar_hsa_circ_92246,RMVar_hsa_circ_117554,RMVar_hsa_circ_147690,RMVar_hsa_circ_147691,RMVar_hsa_circ_147692,RMVar_hsa_circ_374371,RMVar_hsa_circ_147694,RMVar_hsa_circ_372984,RMVar_hsa_circ_147693,RMVar_hsa_circ_357330,RMVar_hsa_circ_97199,RMVar_hsa_circ_95967,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_147701,RMVar_hsa_circ_101460,RMVar_hsa_circ_301735,RMVar_hsa_circ_91945,RMVar_hsa_circ_147713,RMVar_hsa_circ_78263,RMVar_hsa_circ_147709,RMVar_hsa_circ_147708,RMVar_hsa_circ_333940,RMVar_hsa_circ_147712,RMVar_hsa_circ_348744,RMVar_hsa_circ_373682,RMVar_hsa_circ_346114,RMVar_hsa_circ_68884,RMVar_hsa_circ_114985,RMVar_hsa_circ_147714 4333 RMVar_ID_4333 Human_SNP_ID_453923089 A-to-I Human chr11 - 3756996 3756993 3756996 GCAAGCTCCGCTTCCCGGGTTCACACCATTCTACTGCCTCAGCCTCCCAAGTAGCTGGGACTGTA GCAAGCTCCGCTTCCCGGGTTCACACCATTCT___GCCTCAGCCTCCCAAGTAGCTGGGACTGTA CAGT C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs987676277 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_11614903 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_97527,RMVar_hsa_circ_37210,RMVar_hsa_circ_38524,RMVar_hsa_circ_12367,RMVar_hsa_circ_147652,RMVar_hsa_circ_77589,RMVar_hsa_circ_106281,RMVar_hsa_circ_147654,RMVar_hsa_circ_147661,RMVar_hsa_circ_147658,RMVar_hsa_circ_109567,RMVar_hsa_circ_147659,RMVar_hsa_circ_125448,RMVar_hsa_circ_123681,RMVar_hsa_circ_147660,RMVar_hsa_circ_128055,RMVar_hsa_circ_126244,RMVar_hsa_circ_83167,RMVar_hsa_circ_50353,RMVar_hsa_circ_147670,RMVar_hsa_circ_147671,RMVar_hsa_circ_147669,RMVar_hsa_circ_106002,RMVar_hsa_circ_67070,RMVar_hsa_circ_68815,RMVar_hsa_circ_147680,RMVar_hsa_circ_373076,RMVar_hsa_circ_120713,RMVar_hsa_circ_147684,RMVar_hsa_circ_147685,RMVar_hsa_circ_85220,RMVar_hsa_circ_84143,RMVar_hsa_circ_121259,RMVar_hsa_circ_147686,RMVar_hsa_circ_101156,RMVar_hsa_circ_65040,RMVar_hsa_circ_92246,RMVar_hsa_circ_117554,RMVar_hsa_circ_147690,RMVar_hsa_circ_147691,RMVar_hsa_circ_147692,RMVar_hsa_circ_374371,RMVar_hsa_circ_147694,RMVar_hsa_circ_372984,RMVar_hsa_circ_147693,RMVar_hsa_circ_357330,RMVar_hsa_circ_97199,RMVar_hsa_circ_95967,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_147701,RMVar_hsa_circ_101460,RMVar_hsa_circ_301735,RMVar_hsa_circ_91945,RMVar_hsa_circ_147713,RMVar_hsa_circ_78263,RMVar_hsa_circ_147709,RMVar_hsa_circ_147708,RMVar_hsa_circ_333940,RMVar_hsa_circ_147712,RMVar_hsa_circ_348744,RMVar_hsa_circ_373682,RMVar_hsa_circ_346114,RMVar_hsa_circ_68884,RMVar_hsa_circ_114985,RMVar_hsa_circ_147714 4334 RMVar_ID_4334 Human_SNP_ID_453923235 A-to-I Human chr11 - 3757316 3757315 3757317 CACCTGGCTAATTTTTGTGTTTTTGTAGAGACAGGGTTTGCCATGTCACCCAGGCTGGCCTCGAA CACCTGGCTAATTTTTGTGTTTTTGTAGAGA__GGGTTTGCCATGTCACCCAGGCTGGCCTCGAA CTG C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1242501907 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_108729,Human_RBP_ID_11614919 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_97527,RMVar_hsa_circ_37210,RMVar_hsa_circ_38524,RMVar_hsa_circ_12367,RMVar_hsa_circ_147652,RMVar_hsa_circ_77589,RMVar_hsa_circ_106281,RMVar_hsa_circ_147654,RMVar_hsa_circ_147661,RMVar_hsa_circ_147658,RMVar_hsa_circ_109567,RMVar_hsa_circ_147659,RMVar_hsa_circ_125448,RMVar_hsa_circ_123681,RMVar_hsa_circ_147660,RMVar_hsa_circ_128055,RMVar_hsa_circ_126244,RMVar_hsa_circ_83167,RMVar_hsa_circ_50353,RMVar_hsa_circ_147670,RMVar_hsa_circ_147671,RMVar_hsa_circ_147669,RMVar_hsa_circ_106002,RMVar_hsa_circ_67070,RMVar_hsa_circ_68815,RMVar_hsa_circ_147680,RMVar_hsa_circ_373076,RMVar_hsa_circ_120713,RMVar_hsa_circ_147684,RMVar_hsa_circ_147685,RMVar_hsa_circ_85220,RMVar_hsa_circ_84143,RMVar_hsa_circ_121259,RMVar_hsa_circ_147686,RMVar_hsa_circ_101156,RMVar_hsa_circ_65040,RMVar_hsa_circ_92246,RMVar_hsa_circ_117554,RMVar_hsa_circ_147690,RMVar_hsa_circ_147691,RMVar_hsa_circ_147692,RMVar_hsa_circ_374371,RMVar_hsa_circ_147694,RMVar_hsa_circ_372984,RMVar_hsa_circ_147693,RMVar_hsa_circ_357330,RMVar_hsa_circ_97199,RMVar_hsa_circ_95967,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_147701,RMVar_hsa_circ_101460,RMVar_hsa_circ_301735,RMVar_hsa_circ_91945,RMVar_hsa_circ_147713,RMVar_hsa_circ_78263,RMVar_hsa_circ_147709,RMVar_hsa_circ_147708,RMVar_hsa_circ_333940,RMVar_hsa_circ_147712,RMVar_hsa_circ_348744,RMVar_hsa_circ_373682,RMVar_hsa_circ_346114,RMVar_hsa_circ_68884,RMVar_hsa_circ_114985,RMVar_hsa_circ_147714 4335 RMVar_ID_4335 Human_SNP_ID_453923236 A-to-I Human chr11 - 3757316 3757316 3757316 CACCTGGCTAATTTTTGTGTTTTTGTAGAGACAGGGTTTGCCATGTCACCCAGGCTGGCCTCGAA CACCTGGCTAATTTTTGTGTTTTTGTAGAGACGGGGTTTGCCATGTCACCCAGGCTGGCCTCGAA T C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1201165040 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_108729,Human_RBP_ID_11614919 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_97527,RMVar_hsa_circ_37210,RMVar_hsa_circ_38524,RMVar_hsa_circ_12367,RMVar_hsa_circ_147652,RMVar_hsa_circ_77589,RMVar_hsa_circ_106281,RMVar_hsa_circ_147654,RMVar_hsa_circ_147661,RMVar_hsa_circ_147658,RMVar_hsa_circ_109567,RMVar_hsa_circ_147659,RMVar_hsa_circ_125448,RMVar_hsa_circ_123681,RMVar_hsa_circ_147660,RMVar_hsa_circ_128055,RMVar_hsa_circ_126244,RMVar_hsa_circ_83167,RMVar_hsa_circ_50353,RMVar_hsa_circ_147670,RMVar_hsa_circ_147671,RMVar_hsa_circ_147669,RMVar_hsa_circ_106002,RMVar_hsa_circ_67070,RMVar_hsa_circ_68815,RMVar_hsa_circ_147680,RMVar_hsa_circ_373076,RMVar_hsa_circ_120713,RMVar_hsa_circ_147684,RMVar_hsa_circ_147685,RMVar_hsa_circ_85220,RMVar_hsa_circ_84143,RMVar_hsa_circ_121259,RMVar_hsa_circ_147686,RMVar_hsa_circ_101156,RMVar_hsa_circ_65040,RMVar_hsa_circ_92246,RMVar_hsa_circ_117554,RMVar_hsa_circ_147690,RMVar_hsa_circ_147691,RMVar_hsa_circ_147692,RMVar_hsa_circ_374371,RMVar_hsa_circ_147694,RMVar_hsa_circ_372984,RMVar_hsa_circ_147693,RMVar_hsa_circ_357330,RMVar_hsa_circ_97199,RMVar_hsa_circ_95967,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_147701,RMVar_hsa_circ_101460,RMVar_hsa_circ_301735,RMVar_hsa_circ_91945,RMVar_hsa_circ_147713,RMVar_hsa_circ_78263,RMVar_hsa_circ_147709,RMVar_hsa_circ_147708,RMVar_hsa_circ_333940,RMVar_hsa_circ_147712,RMVar_hsa_circ_348744,RMVar_hsa_circ_373682,RMVar_hsa_circ_346114,RMVar_hsa_circ_68884,RMVar_hsa_circ_114985,RMVar_hsa_circ_147714 4336 RMVar_ID_4336 Human_SNP_ID_453923504 A-to-I Human chr11 - 3758199 3758199 3758199 CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACGGGCACCCACCACCACCCCCGGCTAATTTTT CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTGCGGGCACCCACCACCACCCCCGGCTAATTTTT T C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1448689150 Functional Loss SNV dbSNP153 33..33 33 - - - 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_97527,RMVar_hsa_circ_37210,RMVar_hsa_circ_38524,RMVar_hsa_circ_12367,RMVar_hsa_circ_147652,RMVar_hsa_circ_77589,RMVar_hsa_circ_106281,RMVar_hsa_circ_147654,RMVar_hsa_circ_147661,RMVar_hsa_circ_147658,RMVar_hsa_circ_109567,RMVar_hsa_circ_147659,RMVar_hsa_circ_125448,RMVar_hsa_circ_123681,RMVar_hsa_circ_147660,RMVar_hsa_circ_128055,RMVar_hsa_circ_126244,RMVar_hsa_circ_83167,RMVar_hsa_circ_50353,RMVar_hsa_circ_147670,RMVar_hsa_circ_147671,RMVar_hsa_circ_147669,RMVar_hsa_circ_106002,RMVar_hsa_circ_67070,RMVar_hsa_circ_68815,RMVar_hsa_circ_147680,RMVar_hsa_circ_373076,RMVar_hsa_circ_120713,RMVar_hsa_circ_147684,RMVar_hsa_circ_147685,RMVar_hsa_circ_85220,RMVar_hsa_circ_84143,RMVar_hsa_circ_121259,RMVar_hsa_circ_147686,RMVar_hsa_circ_101156,RMVar_hsa_circ_65040,RMVar_hsa_circ_92246,RMVar_hsa_circ_117554,RMVar_hsa_circ_147690,RMVar_hsa_circ_147691,RMVar_hsa_circ_147692,RMVar_hsa_circ_374371,RMVar_hsa_circ_147694,RMVar_hsa_circ_372984,RMVar_hsa_circ_147693,RMVar_hsa_circ_357330,RMVar_hsa_circ_97199,RMVar_hsa_circ_95967,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_147701,RMVar_hsa_circ_101460,RMVar_hsa_circ_301735,RMVar_hsa_circ_91945,RMVar_hsa_circ_147713,RMVar_hsa_circ_78263,RMVar_hsa_circ_147709,RMVar_hsa_circ_147708,RMVar_hsa_circ_333940,RMVar_hsa_circ_147712,RMVar_hsa_circ_348744,RMVar_hsa_circ_373682,RMVar_hsa_circ_346114,RMVar_hsa_circ_68884,RMVar_hsa_circ_114985,RMVar_hsa_circ_147714 4337 RMVar_ID_4337 Human_SNP_ID_453923513 A-to-I Human chr11 - 3758234 3758234 3758234 TCACTGCAAGCCCTGCCTCCTGGGTTCACGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGA TCACTGCAAGCCCTGCCTCCTGGGTTCACGCCTTTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGA T A NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1361748922 Functional Loss SNV dbSNP153 33..33 33 - - - 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_97527,RMVar_hsa_circ_37210,RMVar_hsa_circ_38524,RMVar_hsa_circ_12367,RMVar_hsa_circ_147652,RMVar_hsa_circ_77589,RMVar_hsa_circ_106281,RMVar_hsa_circ_147654,RMVar_hsa_circ_147661,RMVar_hsa_circ_147658,RMVar_hsa_circ_109567,RMVar_hsa_circ_147659,RMVar_hsa_circ_125448,RMVar_hsa_circ_123681,RMVar_hsa_circ_147660,RMVar_hsa_circ_128055,RMVar_hsa_circ_126244,RMVar_hsa_circ_83167,RMVar_hsa_circ_50353,RMVar_hsa_circ_147670,RMVar_hsa_circ_147671,RMVar_hsa_circ_147669,RMVar_hsa_circ_106002,RMVar_hsa_circ_67070,RMVar_hsa_circ_68815,RMVar_hsa_circ_147680,RMVar_hsa_circ_373076,RMVar_hsa_circ_120713,RMVar_hsa_circ_147684,RMVar_hsa_circ_147685,RMVar_hsa_circ_85220,RMVar_hsa_circ_84143,RMVar_hsa_circ_121259,RMVar_hsa_circ_147686,RMVar_hsa_circ_101156,RMVar_hsa_circ_65040,RMVar_hsa_circ_92246,RMVar_hsa_circ_117554,RMVar_hsa_circ_147690,RMVar_hsa_circ_147691,RMVar_hsa_circ_147692,RMVar_hsa_circ_374371,RMVar_hsa_circ_147694,RMVar_hsa_circ_372984,RMVar_hsa_circ_147693,RMVar_hsa_circ_357330,RMVar_hsa_circ_97199,RMVar_hsa_circ_95967,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_147701,RMVar_hsa_circ_101460,RMVar_hsa_circ_301735,RMVar_hsa_circ_91945,RMVar_hsa_circ_147713,RMVar_hsa_circ_78263,RMVar_hsa_circ_147709,RMVar_hsa_circ_147708,RMVar_hsa_circ_333940,RMVar_hsa_circ_147712,RMVar_hsa_circ_348744,RMVar_hsa_circ_373682,RMVar_hsa_circ_346114,RMVar_hsa_circ_68884,RMVar_hsa_circ_114985,RMVar_hsa_circ_147714 4338 RMVar_ID_4338 Human_SNP_ID_453923514 A-to-I Human chr11 - 3758234 3758234 3758234 TCACTGCAAGCCCTGCCTCCTGGGTTCACGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGA TCACTGCAAGCCCTGCCTCCTGGGTTCACGCCGTTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGA T C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1361748922 Functional Loss SNV dbSNP153 33..33 33 - - - 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_97527,RMVar_hsa_circ_37210,RMVar_hsa_circ_38524,RMVar_hsa_circ_12367,RMVar_hsa_circ_147652,RMVar_hsa_circ_77589,RMVar_hsa_circ_106281,RMVar_hsa_circ_147654,RMVar_hsa_circ_147661,RMVar_hsa_circ_147658,RMVar_hsa_circ_109567,RMVar_hsa_circ_147659,RMVar_hsa_circ_125448,RMVar_hsa_circ_123681,RMVar_hsa_circ_147660,RMVar_hsa_circ_128055,RMVar_hsa_circ_126244,RMVar_hsa_circ_83167,RMVar_hsa_circ_50353,RMVar_hsa_circ_147670,RMVar_hsa_circ_147671,RMVar_hsa_circ_147669,RMVar_hsa_circ_106002,RMVar_hsa_circ_67070,RMVar_hsa_circ_68815,RMVar_hsa_circ_147680,RMVar_hsa_circ_373076,RMVar_hsa_circ_120713,RMVar_hsa_circ_147684,RMVar_hsa_circ_147685,RMVar_hsa_circ_85220,RMVar_hsa_circ_84143,RMVar_hsa_circ_121259,RMVar_hsa_circ_147686,RMVar_hsa_circ_101156,RMVar_hsa_circ_65040,RMVar_hsa_circ_92246,RMVar_hsa_circ_117554,RMVar_hsa_circ_147690,RMVar_hsa_circ_147691,RMVar_hsa_circ_147692,RMVar_hsa_circ_374371,RMVar_hsa_circ_147694,RMVar_hsa_circ_372984,RMVar_hsa_circ_147693,RMVar_hsa_circ_357330,RMVar_hsa_circ_97199,RMVar_hsa_circ_95967,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_147701,RMVar_hsa_circ_101460,RMVar_hsa_circ_301735,RMVar_hsa_circ_91945,RMVar_hsa_circ_147713,RMVar_hsa_circ_78263,RMVar_hsa_circ_147709,RMVar_hsa_circ_147708,RMVar_hsa_circ_333940,RMVar_hsa_circ_147712,RMVar_hsa_circ_348744,RMVar_hsa_circ_373682,RMVar_hsa_circ_346114,RMVar_hsa_circ_68884,RMVar_hsa_circ_114985,RMVar_hsa_circ_147714 4339 RMVar_ID_4339 Human_SNP_ID_453923630 A-to-I Human chr11 - 3758593 3758593 3758593 TAAAGTAGAGATGGGGTTTCACCGTGTTGGCGAGGCTGGTTTTGAACTCCTGACCTCAGGCGATC TAAAGTAGAGATGGGGTTTCACCGTGTTGGCGGGGCTGGTTTTGAACTCCTGACCTCAGGCGATC T C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs529249599 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11614991 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_97527,RMVar_hsa_circ_37210,RMVar_hsa_circ_38524,RMVar_hsa_circ_12367,RMVar_hsa_circ_147652,RMVar_hsa_circ_77589,RMVar_hsa_circ_106281,RMVar_hsa_circ_147654,RMVar_hsa_circ_147661,RMVar_hsa_circ_147658,RMVar_hsa_circ_109567,RMVar_hsa_circ_147659,RMVar_hsa_circ_125448,RMVar_hsa_circ_123681,RMVar_hsa_circ_147660,RMVar_hsa_circ_128055,RMVar_hsa_circ_126244,RMVar_hsa_circ_83167,RMVar_hsa_circ_50353,RMVar_hsa_circ_147670,RMVar_hsa_circ_147671,RMVar_hsa_circ_147669,RMVar_hsa_circ_106002,RMVar_hsa_circ_67070,RMVar_hsa_circ_68815,RMVar_hsa_circ_147680,RMVar_hsa_circ_373076,RMVar_hsa_circ_120713,RMVar_hsa_circ_147684,RMVar_hsa_circ_147685,RMVar_hsa_circ_85220,RMVar_hsa_circ_84143,RMVar_hsa_circ_121259,RMVar_hsa_circ_147686,RMVar_hsa_circ_101156,RMVar_hsa_circ_65040,RMVar_hsa_circ_92246,RMVar_hsa_circ_117554,RMVar_hsa_circ_147690,RMVar_hsa_circ_147691,RMVar_hsa_circ_147692,RMVar_hsa_circ_374371,RMVar_hsa_circ_147694,RMVar_hsa_circ_372984,RMVar_hsa_circ_147693,RMVar_hsa_circ_357330,RMVar_hsa_circ_97199,RMVar_hsa_circ_95967,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_147701,RMVar_hsa_circ_101460,RMVar_hsa_circ_301735,RMVar_hsa_circ_91945,RMVar_hsa_circ_147713,RMVar_hsa_circ_78263,RMVar_hsa_circ_147709,RMVar_hsa_circ_147708,RMVar_hsa_circ_333940,RMVar_hsa_circ_147712,RMVar_hsa_circ_348744,RMVar_hsa_circ_373682,RMVar_hsa_circ_346114,RMVar_hsa_circ_68884,RMVar_hsa_circ_114985,RMVar_hsa_circ_147714 4340 RMVar_ID_4340 Human_SNP_ID_453923895 A-to-I Human chr11 - 3759534 3759534 3759534 CAGTGGCATGATCTCGATCTTGGCTCACTGCAAACTCTGCCTCCCGGGTTCAAGCGATTCTCCTG CAGTGGCATGATCTCGATCTTGGCTCACTGCAGACTCTGCCTCCCGGGTTCAAGCGATTCTCCTG T C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1398038496 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11615046 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_97527,RMVar_hsa_circ_37210,RMVar_hsa_circ_38524,RMVar_hsa_circ_12367,RMVar_hsa_circ_147652,RMVar_hsa_circ_77589,RMVar_hsa_circ_106281,RMVar_hsa_circ_147654,RMVar_hsa_circ_147661,RMVar_hsa_circ_147658,RMVar_hsa_circ_109567,RMVar_hsa_circ_147659,RMVar_hsa_circ_125448,RMVar_hsa_circ_123681,RMVar_hsa_circ_147660,RMVar_hsa_circ_128055,RMVar_hsa_circ_126244,RMVar_hsa_circ_83167,RMVar_hsa_circ_50353,RMVar_hsa_circ_147670,RMVar_hsa_circ_147671,RMVar_hsa_circ_147669,RMVar_hsa_circ_106002,RMVar_hsa_circ_67070,RMVar_hsa_circ_68815,RMVar_hsa_circ_147680,RMVar_hsa_circ_373076,RMVar_hsa_circ_120713,RMVar_hsa_circ_147684,RMVar_hsa_circ_147685,RMVar_hsa_circ_85220,RMVar_hsa_circ_84143,RMVar_hsa_circ_121259,RMVar_hsa_circ_147686,RMVar_hsa_circ_101156,RMVar_hsa_circ_65040,RMVar_hsa_circ_92246,RMVar_hsa_circ_117554,RMVar_hsa_circ_147690,RMVar_hsa_circ_147691,RMVar_hsa_circ_147692,RMVar_hsa_circ_374371,RMVar_hsa_circ_147694,RMVar_hsa_circ_372984,RMVar_hsa_circ_147693,RMVar_hsa_circ_357330,RMVar_hsa_circ_97199,RMVar_hsa_circ_95967,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_147701,RMVar_hsa_circ_101460,RMVar_hsa_circ_301735,RMVar_hsa_circ_91945,RMVar_hsa_circ_147713,RMVar_hsa_circ_78263,RMVar_hsa_circ_147709,RMVar_hsa_circ_147708,RMVar_hsa_circ_333940,RMVar_hsa_circ_147712,RMVar_hsa_circ_348744,RMVar_hsa_circ_373682,RMVar_hsa_circ_346114,RMVar_hsa_circ_68884,RMVar_hsa_circ_114985,RMVar_hsa_circ_147714 4341 RMVar_ID_4341 Human_SNP_ID_453923982 A-to-I Human chr11 - 3759881 3759881 3759881 CACACTTGTGAATTGCCACTGCATTCCAGCCTAGGCAACATAGTGAAAGTAGGTCTCTAAAAAAA CACACTTGTGAATTGCCACTGCATTCCAGCCTGGGCAACATAGTGAAAGTAGGTCTCTAAAAAAA T C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1476303135 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11615059,Human_RBP_ID_22890604 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_97527,RMVar_hsa_circ_37210,RMVar_hsa_circ_38524,RMVar_hsa_circ_12367,RMVar_hsa_circ_147652,RMVar_hsa_circ_77589,RMVar_hsa_circ_106281,RMVar_hsa_circ_147654,RMVar_hsa_circ_147661,RMVar_hsa_circ_147658,RMVar_hsa_circ_109567,RMVar_hsa_circ_147659,RMVar_hsa_circ_125448,RMVar_hsa_circ_123681,RMVar_hsa_circ_147660,RMVar_hsa_circ_128055,RMVar_hsa_circ_126244,RMVar_hsa_circ_83167,RMVar_hsa_circ_50353,RMVar_hsa_circ_147670,RMVar_hsa_circ_147671,RMVar_hsa_circ_147669,RMVar_hsa_circ_106002,RMVar_hsa_circ_67070,RMVar_hsa_circ_68815,RMVar_hsa_circ_147680,RMVar_hsa_circ_373076,RMVar_hsa_circ_120713,RMVar_hsa_circ_147684,RMVar_hsa_circ_147685,RMVar_hsa_circ_85220,RMVar_hsa_circ_84143,RMVar_hsa_circ_121259,RMVar_hsa_circ_147686,RMVar_hsa_circ_101156,RMVar_hsa_circ_65040,RMVar_hsa_circ_92246,RMVar_hsa_circ_117554,RMVar_hsa_circ_147690,RMVar_hsa_circ_147691,RMVar_hsa_circ_147692,RMVar_hsa_circ_374371,RMVar_hsa_circ_147694,RMVar_hsa_circ_372984,RMVar_hsa_circ_147693,RMVar_hsa_circ_357330,RMVar_hsa_circ_97199,RMVar_hsa_circ_95967,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_147701,RMVar_hsa_circ_101460,RMVar_hsa_circ_301735,RMVar_hsa_circ_91945,RMVar_hsa_circ_147713,RMVar_hsa_circ_78263,RMVar_hsa_circ_147709,RMVar_hsa_circ_147708,RMVar_hsa_circ_333940,RMVar_hsa_circ_147712,RMVar_hsa_circ_348744,RMVar_hsa_circ_373682,RMVar_hsa_circ_346114,RMVar_hsa_circ_68884,RMVar_hsa_circ_114985,RMVar_hsa_circ_147714 4342 RMVar_ID_4342 Human_SNP_ID_453924638 A-to-I Human chr11 - 3762202 3762202 3762202 GAGATGCTGAGGCAAGAGAATCACTTGAACCCAGGAAGTGGAGGTTGCAGTGACCCGAGATCGCG GAGATGCTGAGGCAAGAGAATCACTTGAACCCGGGAAGTGGAGGTTGCAGTGACCCGAGATCGCG T C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs996386974 Functional Loss SNV dbSNP153 33..33 33 - - - 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_97527,RMVar_hsa_circ_37210,RMVar_hsa_circ_38524,RMVar_hsa_circ_12367,RMVar_hsa_circ_147652,RMVar_hsa_circ_77589,RMVar_hsa_circ_106281,RMVar_hsa_circ_147654,RMVar_hsa_circ_147661,RMVar_hsa_circ_147658,RMVar_hsa_circ_109567,RMVar_hsa_circ_147659,RMVar_hsa_circ_125448,RMVar_hsa_circ_123681,RMVar_hsa_circ_147660,RMVar_hsa_circ_128055,RMVar_hsa_circ_126244,RMVar_hsa_circ_83167,RMVar_hsa_circ_147670,RMVar_hsa_circ_147671,RMVar_hsa_circ_147669,RMVar_hsa_circ_106002,RMVar_hsa_circ_67070,RMVar_hsa_circ_68815,RMVar_hsa_circ_147680,RMVar_hsa_circ_373076,RMVar_hsa_circ_120713,RMVar_hsa_circ_147684,RMVar_hsa_circ_147685,RMVar_hsa_circ_85220,RMVar_hsa_circ_84143,RMVar_hsa_circ_121259,RMVar_hsa_circ_147686,RMVar_hsa_circ_101156,RMVar_hsa_circ_65040,RMVar_hsa_circ_92246,RMVar_hsa_circ_117554,RMVar_hsa_circ_147690,RMVar_hsa_circ_147691,RMVar_hsa_circ_147692,RMVar_hsa_circ_372984,RMVar_hsa_circ_147693,RMVar_hsa_circ_357330,RMVar_hsa_circ_97199,RMVar_hsa_circ_95967,RMVar_hsa_circ_147702,RMVar_hsa_circ_147706,RMVar_hsa_circ_82731,RMVar_hsa_circ_83071,RMVar_hsa_circ_147707,RMVar_hsa_circ_147704,RMVar_hsa_circ_147705,RMVar_hsa_circ_147703,RMVar_hsa_circ_147701,RMVar_hsa_circ_101460,RMVar_hsa_circ_91945,RMVar_hsa_circ_147713,RMVar_hsa_circ_78263,RMVar_hsa_circ_147709,RMVar_hsa_circ_147708,RMVar_hsa_circ_333940,RMVar_hsa_circ_147712,RMVar_hsa_circ_348744,RMVar_hsa_circ_373682,RMVar_hsa_circ_346114,RMVar_hsa_circ_68884,RMVar_hsa_circ_114985,RMVar_hsa_circ_147714,RMVar_hsa_circ_147715,RMVar_hsa_circ_353054,RMVar_hsa_circ_359731,RMVar_hsa_circ_92677,RMVar_hsa_circ_366821 4343 RMVar_ID_4343 Human_SNP_ID_453924647 A-to-I Human chr11 - 3762238 3762238 3762238 GGGTGTGGTGGTGGGTGCCTGTAATACCAGCTACTTGAGATGCTGAGGCAAGAGAATCACTTGAA GGGTGTGGTGGTGGGTGCCTGTAATACCAGCTGCTTGAGATGCTGAGGCAAGAGAATCACTTGAA T C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1356950648 Functional Loss SNV dbSNP153 33..33 33 - - - 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_97527,RMVar_hsa_circ_37210,RMVar_hsa_circ_38524,RMVar_hsa_circ_12367,RMVar_hsa_circ_147652,RMVar_hsa_circ_77589,RMVar_hsa_circ_106281,RMVar_hsa_circ_147654,RMVar_hsa_circ_147661,RMVar_hsa_circ_147658,RMVar_hsa_circ_109567,RMVar_hsa_circ_147659,RMVar_hsa_circ_125448,RMVar_hsa_circ_123681,RMVar_hsa_circ_147660,RMVar_hsa_circ_128055,RMVar_hsa_circ_126244,RMVar_hsa_circ_83167,RMVar_hsa_circ_147670,RMVar_hsa_circ_147671,RMVar_hsa_circ_147669,RMVar_hsa_circ_106002,RMVar_hsa_circ_67070,RMVar_hsa_circ_68815,RMVar_hsa_circ_147680,RMVar_hsa_circ_373076,RMVar_hsa_circ_120713,RMVar_hsa_circ_147684,RMVar_hsa_circ_147685,RMVar_hsa_circ_85220,RMVar_hsa_circ_84143,RMVar_hsa_circ_121259,RMVar_hsa_circ_147686,RMVar_hsa_circ_101156,RMVar_hsa_circ_65040,RMVar_hsa_circ_92246,RMVar_hsa_circ_117554,RMVar_hsa_circ_147690,RMVar_hsa_circ_147691,RMVar_hsa_circ_147692,RMVar_hsa_circ_372984,RMVar_hsa_circ_147693,RMVar_hsa_circ_357330,RMVar_hsa_circ_97199,RMVar_hsa_circ_95967,RMVar_hsa_circ_147702,RMVar_hsa_circ_147706,RMVar_hsa_circ_82731,RMVar_hsa_circ_83071,RMVar_hsa_circ_147707,RMVar_hsa_circ_147704,RMVar_hsa_circ_147705,RMVar_hsa_circ_147703,RMVar_hsa_circ_147701,RMVar_hsa_circ_101460,RMVar_hsa_circ_91945,RMVar_hsa_circ_147713,RMVar_hsa_circ_78263,RMVar_hsa_circ_147709,RMVar_hsa_circ_147708,RMVar_hsa_circ_333940,RMVar_hsa_circ_147712,RMVar_hsa_circ_348744,RMVar_hsa_circ_373682,RMVar_hsa_circ_346114,RMVar_hsa_circ_68884,RMVar_hsa_circ_114985,RMVar_hsa_circ_147714,RMVar_hsa_circ_147715,RMVar_hsa_circ_353054,RMVar_hsa_circ_359731,RMVar_hsa_circ_92677,RMVar_hsa_circ_366821 4344 RMVar_ID_4344 Human_SNP_ID_453924648 A-to-I Human chr11 - 3762238 3762238 3762238 GGGTGTGGTGGTGGGTGCCTGTAATACCAGCTACTTGAGATGCTGAGGCAAGAGAATCACTTGAA GGGTGTGGTGGTGGGTGCCTGTAATACCAGCTCCTTGAGATGCTGAGGCAAGAGAATCACTTGAA T G NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1356950648 Functional Loss SNV dbSNP153 33..33 33 - - - 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_97527,RMVar_hsa_circ_37210,RMVar_hsa_circ_38524,RMVar_hsa_circ_12367,RMVar_hsa_circ_147652,RMVar_hsa_circ_77589,RMVar_hsa_circ_106281,RMVar_hsa_circ_147654,RMVar_hsa_circ_147661,RMVar_hsa_circ_147658,RMVar_hsa_circ_109567,RMVar_hsa_circ_147659,RMVar_hsa_circ_125448,RMVar_hsa_circ_123681,RMVar_hsa_circ_147660,RMVar_hsa_circ_128055,RMVar_hsa_circ_126244,RMVar_hsa_circ_83167,RMVar_hsa_circ_147670,RMVar_hsa_circ_147671,RMVar_hsa_circ_147669,RMVar_hsa_circ_106002,RMVar_hsa_circ_67070,RMVar_hsa_circ_68815,RMVar_hsa_circ_147680,RMVar_hsa_circ_373076,RMVar_hsa_circ_120713,RMVar_hsa_circ_147684,RMVar_hsa_circ_147685,RMVar_hsa_circ_85220,RMVar_hsa_circ_84143,RMVar_hsa_circ_121259,RMVar_hsa_circ_147686,RMVar_hsa_circ_101156,RMVar_hsa_circ_65040,RMVar_hsa_circ_92246,RMVar_hsa_circ_117554,RMVar_hsa_circ_147690,RMVar_hsa_circ_147691,RMVar_hsa_circ_147692,RMVar_hsa_circ_372984,RMVar_hsa_circ_147693,RMVar_hsa_circ_357330,RMVar_hsa_circ_97199,RMVar_hsa_circ_95967,RMVar_hsa_circ_147702,RMVar_hsa_circ_147706,RMVar_hsa_circ_82731,RMVar_hsa_circ_83071,RMVar_hsa_circ_147707,RMVar_hsa_circ_147704,RMVar_hsa_circ_147705,RMVar_hsa_circ_147703,RMVar_hsa_circ_147701,RMVar_hsa_circ_101460,RMVar_hsa_circ_91945,RMVar_hsa_circ_147713,RMVar_hsa_circ_78263,RMVar_hsa_circ_147709,RMVar_hsa_circ_147708,RMVar_hsa_circ_333940,RMVar_hsa_circ_147712,RMVar_hsa_circ_348744,RMVar_hsa_circ_373682,RMVar_hsa_circ_346114,RMVar_hsa_circ_68884,RMVar_hsa_circ_114985,RMVar_hsa_circ_147714,RMVar_hsa_circ_147715,RMVar_hsa_circ_353054,RMVar_hsa_circ_359731,RMVar_hsa_circ_92677,RMVar_hsa_circ_366821 4345 RMVar_ID_4345 Human_SNP_ID_453925510 A-to-I Human chr11 - 3765284 3765284 3765284 AGGTCGGGGAATCATTGAGGTCATGAGTTAGAAGCTGTGGTGCACTATGATCGTGGCTATGAATA AGGTCGGGGAATCATTGAGGTCATGAGTTAGAGGCTGTGGTGCACTATGATCGTGGCTATGAATA T C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559115852 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11615165 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_147639,RMVar_hsa_circ_97527,RMVar_hsa_circ_37210,RMVar_hsa_circ_12367,RMVar_hsa_circ_147652,RMVar_hsa_circ_77589,RMVar_hsa_circ_106281,RMVar_hsa_circ_147654,RMVar_hsa_circ_147661,RMVar_hsa_circ_147658,RMVar_hsa_circ_109567,RMVar_hsa_circ_147659,RMVar_hsa_circ_125448,RMVar_hsa_circ_123681,RMVar_hsa_circ_147660,RMVar_hsa_circ_128055,RMVar_hsa_circ_126244,RMVar_hsa_circ_83167,RMVar_hsa_circ_147670,RMVar_hsa_circ_147671,RMVar_hsa_circ_147669,RMVar_hsa_circ_106002,RMVar_hsa_circ_67070,RMVar_hsa_circ_68815,RMVar_hsa_circ_147680,RMVar_hsa_circ_373076,RMVar_hsa_circ_120713,RMVar_hsa_circ_147684,RMVar_hsa_circ_147685,RMVar_hsa_circ_85220,RMVar_hsa_circ_84143,RMVar_hsa_circ_121259,RMVar_hsa_circ_147686,RMVar_hsa_circ_101156,RMVar_hsa_circ_92246,RMVar_hsa_circ_117554,RMVar_hsa_circ_147690,RMVar_hsa_circ_147691,RMVar_hsa_circ_147692,RMVar_hsa_circ_147693,RMVar_hsa_circ_357330,RMVar_hsa_circ_97199,RMVar_hsa_circ_95967,RMVar_hsa_circ_147702,RMVar_hsa_circ_147706,RMVar_hsa_circ_82731,RMVar_hsa_circ_83071,RMVar_hsa_circ_147707,RMVar_hsa_circ_147704,RMVar_hsa_circ_147705,RMVar_hsa_circ_147703,RMVar_hsa_circ_101460,RMVar_hsa_circ_91945,RMVar_hsa_circ_147713,RMVar_hsa_circ_78263,RMVar_hsa_circ_147709,RMVar_hsa_circ_147708,RMVar_hsa_circ_333940,RMVar_hsa_circ_147712,RMVar_hsa_circ_348744,RMVar_hsa_circ_373682,RMVar_hsa_circ_346114,RMVar_hsa_circ_114985,RMVar_hsa_circ_147714,RMVar_hsa_circ_147717,RMVar_hsa_circ_292347,RMVar_hsa_circ_147715,RMVar_hsa_circ_353054,RMVar_hsa_circ_359731,RMVar_hsa_circ_92677,RMVar_hsa_circ_366821,RMVar_hsa_circ_294499,RMVar_hsa_circ_362354,RMVar_hsa_circ_369953,RMVar_hsa_circ_294297,RMVar_hsa_circ_147719,RMVar_hsa_circ_271621,RMVar_hsa_circ_147718,RMVar_hsa_circ_147716 4346 RMVar_ID_4346 Human_SNP_ID_453925608 A-to-I Human chr11 - 3765679 3765679 3765679 CTCCTGCCTTGGTCTCCTGAGTAACTGGGATTACAGGTGTGCGCCACCGTGCCCGGCTAATTTTT CTCCTGCCTTGGTCTCCTGAGTAACTGGGATTTCAGGTGTGCGCCACCGTGCCCGGCTAATTTTT T A NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444925837 Functional Loss SNV dbSNP153 33..33 33 - - - 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_147639,RMVar_hsa_circ_97527,RMVar_hsa_circ_37210,RMVar_hsa_circ_12367,RMVar_hsa_circ_147652,RMVar_hsa_circ_77589,RMVar_hsa_circ_106281,RMVar_hsa_circ_147654,RMVar_hsa_circ_147661,RMVar_hsa_circ_147658,RMVar_hsa_circ_109567,RMVar_hsa_circ_147659,RMVar_hsa_circ_125448,RMVar_hsa_circ_123681,RMVar_hsa_circ_147660,RMVar_hsa_circ_128055,RMVar_hsa_circ_126244,RMVar_hsa_circ_83167,RMVar_hsa_circ_147670,RMVar_hsa_circ_147671,RMVar_hsa_circ_147669,RMVar_hsa_circ_106002,RMVar_hsa_circ_67070,RMVar_hsa_circ_68815,RMVar_hsa_circ_147680,RMVar_hsa_circ_373076,RMVar_hsa_circ_120713,RMVar_hsa_circ_147684,RMVar_hsa_circ_147685,RMVar_hsa_circ_85220,RMVar_hsa_circ_84143,RMVar_hsa_circ_121259,RMVar_hsa_circ_147686,RMVar_hsa_circ_101156,RMVar_hsa_circ_92246,RMVar_hsa_circ_117554,RMVar_hsa_circ_147690,RMVar_hsa_circ_147691,RMVar_hsa_circ_147692,RMVar_hsa_circ_147693,RMVar_hsa_circ_357330,RMVar_hsa_circ_97199,RMVar_hsa_circ_95967,RMVar_hsa_circ_147702,RMVar_hsa_circ_147706,RMVar_hsa_circ_82731,RMVar_hsa_circ_83071,RMVar_hsa_circ_147707,RMVar_hsa_circ_147704,RMVar_hsa_circ_147705,RMVar_hsa_circ_147703,RMVar_hsa_circ_101460,RMVar_hsa_circ_91945,RMVar_hsa_circ_147713,RMVar_hsa_circ_78263,RMVar_hsa_circ_147709,RMVar_hsa_circ_147708,RMVar_hsa_circ_333940,RMVar_hsa_circ_147712,RMVar_hsa_circ_348744,RMVar_hsa_circ_373682,RMVar_hsa_circ_346114,RMVar_hsa_circ_114985,RMVar_hsa_circ_147714,RMVar_hsa_circ_147717,RMVar_hsa_circ_292347,RMVar_hsa_circ_147715,RMVar_hsa_circ_353054,RMVar_hsa_circ_359731,RMVar_hsa_circ_92677,RMVar_hsa_circ_366821,RMVar_hsa_circ_294499,RMVar_hsa_circ_362354,RMVar_hsa_circ_369953,RMVar_hsa_circ_294297,RMVar_hsa_circ_147719,RMVar_hsa_circ_271621,RMVar_hsa_circ_147718,RMVar_hsa_circ_147716 4347 RMVar_ID_4347 Human_SNP_ID_453925747 A-to-I Human chr11 - 3766227 3766227 3766227 GGGACTACAGGCGTGCACCACCATGTCCAGCTAATTTTTGTAGTTTTTGTAGAGATGGGTTTTCA GGGACTACAGGCGTGCACCACCATGTCCAGCTTATTTTTGTAGTTTTTGTAGAGATGGGTTTTCA T A NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1324456828 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8351221 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_147639,RMVar_hsa_circ_97527,RMVar_hsa_circ_37210,RMVar_hsa_circ_12367,RMVar_hsa_circ_147652,RMVar_hsa_circ_77589,RMVar_hsa_circ_106281,RMVar_hsa_circ_147654,RMVar_hsa_circ_147661,RMVar_hsa_circ_147658,RMVar_hsa_circ_109567,RMVar_hsa_circ_147659,RMVar_hsa_circ_125448,RMVar_hsa_circ_123681,RMVar_hsa_circ_147660,RMVar_hsa_circ_128055,RMVar_hsa_circ_126244,RMVar_hsa_circ_83167,RMVar_hsa_circ_147670,RMVar_hsa_circ_147671,RMVar_hsa_circ_147669,RMVar_hsa_circ_106002,RMVar_hsa_circ_67070,RMVar_hsa_circ_68815,RMVar_hsa_circ_147680,RMVar_hsa_circ_373076,RMVar_hsa_circ_120713,RMVar_hsa_circ_147684,RMVar_hsa_circ_147685,RMVar_hsa_circ_85220,RMVar_hsa_circ_84143,RMVar_hsa_circ_121259,RMVar_hsa_circ_147686,RMVar_hsa_circ_101156,RMVar_hsa_circ_92246,RMVar_hsa_circ_117554,RMVar_hsa_circ_147690,RMVar_hsa_circ_147691,RMVar_hsa_circ_147692,RMVar_hsa_circ_147693,RMVar_hsa_circ_357330,RMVar_hsa_circ_97199,RMVar_hsa_circ_95967,RMVar_hsa_circ_147702,RMVar_hsa_circ_147706,RMVar_hsa_circ_82731,RMVar_hsa_circ_83071,RMVar_hsa_circ_147707,RMVar_hsa_circ_147704,RMVar_hsa_circ_147705,RMVar_hsa_circ_147703,RMVar_hsa_circ_101460,RMVar_hsa_circ_91945,RMVar_hsa_circ_147713,RMVar_hsa_circ_78263,RMVar_hsa_circ_147709,RMVar_hsa_circ_147708,RMVar_hsa_circ_333940,RMVar_hsa_circ_147712,RMVar_hsa_circ_348744,RMVar_hsa_circ_373682,RMVar_hsa_circ_346114,RMVar_hsa_circ_114985,RMVar_hsa_circ_147714,RMVar_hsa_circ_147717,RMVar_hsa_circ_292347,RMVar_hsa_circ_147715,RMVar_hsa_circ_353054,RMVar_hsa_circ_359731,RMVar_hsa_circ_92677,RMVar_hsa_circ_366821,RMVar_hsa_circ_294499,RMVar_hsa_circ_362354,RMVar_hsa_circ_369953,RMVar_hsa_circ_294297,RMVar_hsa_circ_147719,RMVar_hsa_circ_271621,RMVar_hsa_circ_147718,RMVar_hsa_circ_147716 4348 RMVar_ID_4348 Human_SNP_ID_453925778 A-to-I Human chr11 - 3766321 3766321 3766321 TCACCCAGGCTGGAGTGCAGTGGCATGATCTCAGTTCACTGCGTCCTCCGCCTCCTGGGCTAAGC TCACCCAGGCTGGAGTGCAGTGGCATGATCTCCGTTCACTGCGTCCTCCGCCTCCTGGGCTAAGC T G NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1469729248 Functional Loss SNV dbSNP153 33..33 33 - - - 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_147639,RMVar_hsa_circ_97527,RMVar_hsa_circ_37210,RMVar_hsa_circ_12367,RMVar_hsa_circ_147652,RMVar_hsa_circ_77589,RMVar_hsa_circ_106281,RMVar_hsa_circ_147654,RMVar_hsa_circ_147661,RMVar_hsa_circ_147658,RMVar_hsa_circ_109567,RMVar_hsa_circ_147659,RMVar_hsa_circ_125448,RMVar_hsa_circ_123681,RMVar_hsa_circ_147660,RMVar_hsa_circ_128055,RMVar_hsa_circ_126244,RMVar_hsa_circ_83167,RMVar_hsa_circ_147670,RMVar_hsa_circ_147671,RMVar_hsa_circ_147669,RMVar_hsa_circ_106002,RMVar_hsa_circ_67070,RMVar_hsa_circ_68815,RMVar_hsa_circ_147680,RMVar_hsa_circ_373076,RMVar_hsa_circ_120713,RMVar_hsa_circ_147684,RMVar_hsa_circ_147685,RMVar_hsa_circ_85220,RMVar_hsa_circ_84143,RMVar_hsa_circ_121259,RMVar_hsa_circ_147686,RMVar_hsa_circ_101156,RMVar_hsa_circ_92246,RMVar_hsa_circ_117554,RMVar_hsa_circ_147690,RMVar_hsa_circ_147691,RMVar_hsa_circ_147692,RMVar_hsa_circ_147693,RMVar_hsa_circ_357330,RMVar_hsa_circ_97199,RMVar_hsa_circ_95967,RMVar_hsa_circ_147702,RMVar_hsa_circ_147706,RMVar_hsa_circ_82731,RMVar_hsa_circ_83071,RMVar_hsa_circ_147707,RMVar_hsa_circ_147704,RMVar_hsa_circ_147705,RMVar_hsa_circ_147703,RMVar_hsa_circ_101460,RMVar_hsa_circ_91945,RMVar_hsa_circ_147713,RMVar_hsa_circ_78263,RMVar_hsa_circ_147709,RMVar_hsa_circ_147708,RMVar_hsa_circ_333940,RMVar_hsa_circ_147712,RMVar_hsa_circ_348744,RMVar_hsa_circ_373682,RMVar_hsa_circ_346114,RMVar_hsa_circ_114985,RMVar_hsa_circ_147714,RMVar_hsa_circ_147717,RMVar_hsa_circ_292347,RMVar_hsa_circ_147715,RMVar_hsa_circ_353054,RMVar_hsa_circ_359731,RMVar_hsa_circ_92677,RMVar_hsa_circ_366821,RMVar_hsa_circ_294499,RMVar_hsa_circ_362354,RMVar_hsa_circ_369953,RMVar_hsa_circ_294297,RMVar_hsa_circ_147719,RMVar_hsa_circ_271621,RMVar_hsa_circ_147718,RMVar_hsa_circ_147716 4349 RMVar_ID_4349 Human_SNP_ID_453927188 A-to-I Human chr11 - 3771000 3771000 3771000 AAATTAGCCAGGCGTGGTGACAAGCACCTGTAATCCCAACTACTTGGGAGGCTGAGGCAGGAGAA AAATTAGCCAGGCGTGGTGACAAGCACCTGTACTCCCAACTACTTGGGAGGCTGAGGCAGGAGAA T G NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1030630170 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108806,RMVar_hsa_circ_147635,RMVar_hsa_circ_121348,RMVar_hsa_circ_104783,RMVar_hsa_circ_147640,RMVar_hsa_circ_147639,RMVar_hsa_circ_37210,RMVar_hsa_circ_12367,RMVar_hsa_circ_147661,RMVar_hsa_circ_125448,RMVar_hsa_circ_123681,RMVar_hsa_circ_147660,RMVar_hsa_circ_128055,RMVar_hsa_circ_126244,RMVar_hsa_circ_147670,RMVar_hsa_circ_147669,RMVar_hsa_circ_67070,RMVar_hsa_circ_68815,RMVar_hsa_circ_120713,RMVar_hsa_circ_147685,RMVar_hsa_circ_121259,RMVar_hsa_circ_101156,RMVar_hsa_circ_92246,RMVar_hsa_circ_147691,RMVar_hsa_circ_147692,RMVar_hsa_circ_357330,RMVar_hsa_circ_95967,RMVar_hsa_circ_147706,RMVar_hsa_circ_82731,RMVar_hsa_circ_83071,RMVar_hsa_circ_147707,RMVar_hsa_circ_147704,RMVar_hsa_circ_147705,RMVar_hsa_circ_147703,RMVar_hsa_circ_101460,RMVar_hsa_circ_147708,RMVar_hsa_circ_333940,RMVar_hsa_circ_348744,RMVar_hsa_circ_373682,RMVar_hsa_circ_346114,RMVar_hsa_circ_147714,RMVar_hsa_circ_147717,RMVar_hsa_circ_292347,RMVar_hsa_circ_353054,RMVar_hsa_circ_359731,RMVar_hsa_circ_366821,RMVar_hsa_circ_294499,RMVar_hsa_circ_362354,RMVar_hsa_circ_369953,RMVar_hsa_circ_147719,RMVar_hsa_circ_271621,RMVar_hsa_circ_147718,RMVar_hsa_circ_278148,RMVar_hsa_circ_307401,RMVar_hsa_circ_363765,RMVar_hsa_circ_308135,RMVar_hsa_circ_286614,RMVar_hsa_circ_147721,RMVar_hsa_circ_147723,RMVar_hsa_circ_147724,RMVar_hsa_circ_147722,RMVar_hsa_circ_147720 4350 RMVar_ID_4350 Human_SNP_ID_453930761 A-to-I Human chr11 - 3782655 3782655 3782655 GCTTGTAATCCCAGGTACTTTGAGACTGAGGCAGGAGAATAACTTGAACCAAGGAGGAGGAGGTT GCTTGTAATCCCAGGTACTTTGAGACTGAGGCGGGAGAATAACTTGAACCAAGGAGGAGGAGGTT T C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1187689560 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6072872,Human_RBP_ID_11615500 RMVar_hsa_circ_125448,RMVar_hsa_circ_147660,RMVar_hsa_circ_128055,RMVar_hsa_circ_147669,RMVar_hsa_circ_92246,RMVar_hsa_circ_147707 4351 RMVar_ID_4351 Human_SNP_ID_453930774 A-to-I Human chr11 - 3782699 3782699 3782699 TCTCTCCTAAAAATACAAATAATTAGACAGGCATGGTGACACACGCTTGTAATCCCAGGTACTTT TCTCTCCTAAAAATACAAATAATTAGACAGGCGTGGTGACACACGCTTGTAATCCCAGGTACTTT T C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1052565328 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125448,RMVar_hsa_circ_147660,RMVar_hsa_circ_128055,RMVar_hsa_circ_147669,RMVar_hsa_circ_92246,RMVar_hsa_circ_147707 4352 RMVar_ID_4352 Human_SNP_ID_453932891 A-to-I Human chr11 - 3789632 3789632 3789632 ACATGCCTGTGGTCTCAGCTTTTTGGGAGGCTAAAGTGGGAGGATCAGTTGAACCCAGGAGGTCC ACATGCCTGTGGTCTCAGCTTTTTGGGAGGCTTAAGTGGGAGGATCAGTTGAACCCAGGAGGTCC T A NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1488271950 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125448,RMVar_hsa_circ_147660,RMVar_hsa_circ_128055,RMVar_hsa_circ_147669,RMVar_hsa_circ_92246,RMVar_hsa_circ_147707 4353 RMVar_ID_4353 Human_SNP_ID_453933299 A-to-I Human chr11 - 3790981 3790981 3790981 TGACGCAGGAGAATGTCGTGAACCTGGGAGGCAGAGCTTGCAGTCAGCCGAGATTGCGTCACTTC TGACGCAGGAGAATGTCGTGAACCTGGGAGGCGGAGCTTGCAGTCAGCCGAGATTGCGTCACTTC T C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982581522 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11615806 RMVar_hsa_circ_125448,RMVar_hsa_circ_147660,RMVar_hsa_circ_128055,RMVar_hsa_circ_147669,RMVar_hsa_circ_92246,RMVar_hsa_circ_147707 4354 RMVar_ID_4354 Human_SNP_ID_453933300 A-to-I Human chr11 - 3790981 3790981 3790981 TGACGCAGGAGAATGTCGTGAACCTGGGAGGCAGAGCTTGCAGTCAGCCGAGATTGCGTCACTTC TGACGCAGGAGAATGTCGTGAACCTGGGAGGCCGAGCTTGCAGTCAGCCGAGATTGCGTCACTTC T G NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982581522 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11615806 RMVar_hsa_circ_125448,RMVar_hsa_circ_147660,RMVar_hsa_circ_128055,RMVar_hsa_circ_147669,RMVar_hsa_circ_92246,RMVar_hsa_circ_147707 4355 RMVar_ID_4355 Human_SNP_ID_453933313 A-to-I Human chr11 - 3791017 3791016 3791017 GTGGCGGGCGCCTGTAATCCCAGTTACTCGGAAGGCTGACGCAGGAGAATGTCGTGAACCTGGGA GTGGCGGGCGCCTGTAATCCCAGTTACTCGGA_GGCTGACGCAGGAGAATGTCGTGAACCTGGGA CT C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1462303564 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_125448,RMVar_hsa_circ_147660,RMVar_hsa_circ_128055,RMVar_hsa_circ_147669,RMVar_hsa_circ_92246,RMVar_hsa_circ_147707 4356 RMVar_ID_4356 Human_SNP_ID_453933324 A-to-I Human chr11 - 3791033 3791033 3791033 AAATTAGCTGGGCGTGGTGGCGGGCGCCTGTAATCCCAGTTACTCGGAAGGCTGACGCAGGAGAA AAATTAGCTGGGCGTGGTGGCGGGCGCCTGTAGTCCCAGTTACTCGGAAGGCTGACGCAGGAGAA T C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs374907049 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125448,RMVar_hsa_circ_147660,RMVar_hsa_circ_128055,RMVar_hsa_circ_147669,RMVar_hsa_circ_92246,RMVar_hsa_circ_147707 4357 RMVar_ID_4357 Human_SNP_ID_453933548 A-to-I Human chr11 - 3791482 3791482 3791482 TCCCCCAGGCTGGAGTACAATGGTGGGATCTCAACTCACTGCAACCTCCGCCTTCTGGGTTCCAC TCCCCCAGGCTGGAGTACAATGGTGGGATCTCGACTCACTGCAACCTCCGCCTTCTGGGTTCCAC T C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4910799 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_178,GWAS_ID_179,GWAS_ID_180,GWAS_ID_181,GWAS_ID_182,GWAS_ID_183,GWAS_ID_184,GWAS_ID_185,GWAS_ID_186,GWAS_ID_187,GWAS_ID_188 RMVar_hsa_circ_125448,RMVar_hsa_circ_147660,RMVar_hsa_circ_128055,RMVar_hsa_circ_147669,RMVar_hsa_circ_92246,RMVar_hsa_circ_147707 4358 RMVar_ID_4358 Human_SNP_ID_453933549 A-to-I Human chr11 - 3791482 3791482 3791482 TCCCCCAGGCTGGAGTACAATGGTGGGATCTCAACTCACTGCAACCTCCGCCTTCTGGGTTCCAC TCCCCCAGGCTGGAGTACAATGGTGGGATCTCCACTCACTGCAACCTCCGCCTTCTGGGTTCCAC T G NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4910799 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_178,GWAS_ID_179,GWAS_ID_180,GWAS_ID_181,GWAS_ID_182,GWAS_ID_183,GWAS_ID_184,GWAS_ID_185,GWAS_ID_186,GWAS_ID_187,GWAS_ID_188 RMVar_hsa_circ_125448,RMVar_hsa_circ_147660,RMVar_hsa_circ_128055,RMVar_hsa_circ_147669,RMVar_hsa_circ_92246,RMVar_hsa_circ_147707 4359 RMVar_ID_4359 Human_SNP_ID_453933693 A-to-I Human chr11 - 3791760 3791760 3791760 TCGGCTCACTGTAACCTCGCCTCCTGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCT TCGGCTCACTGTAACCTCGCCTCCTGGGTTCACGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCT T G NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1415084536 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125448,RMVar_hsa_circ_147660,RMVar_hsa_circ_128055,RMVar_hsa_circ_147669,RMVar_hsa_circ_92246,RMVar_hsa_circ_147707 4360 RMVar_ID_4360 Human_SNP_ID_453934022 A-to-I Human chr11 - 3792564 3792564 3792564 CTTTGTCACCCAGGCTGGAGTGTTGTGGCACAATCTTGGCTCACTGTAACCTCTGCATTCCGGGT CTTTGTCACCCAGGCTGGAGTGTTGTGGCACAGTCTTGGCTCACTGTAACCTCTGCATTCCGGGT T C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1259339128 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11615841 RMVar_hsa_circ_125448,RMVar_hsa_circ_147660,RMVar_hsa_circ_128055,RMVar_hsa_circ_147669,RMVar_hsa_circ_92246,RMVar_hsa_circ_147707 4361 RMVar_ID_4361 Human_SNP_ID_453934184 A-to-I Human chr11 - 3793059 3793059 3793059 TCGCCCAAGTCGGAGTGCAGTGGCGCTATCTCAGCGTACTCCAACCTCCGCCTCCCAGGTTCAAG TCGCCCAAGTCGGAGTGCAGTGGCGCTATCTCTGCGTACTCCAACCTCCGCCTCCCAGGTTCAAG T A NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs896296405 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11615861 RMVar_hsa_circ_125448,RMVar_hsa_circ_147660,RMVar_hsa_circ_128055,RMVar_hsa_circ_147669,RMVar_hsa_circ_92246,RMVar_hsa_circ_147707 4362 RMVar_ID_4362 Human_SNP_ID_453934185 A-to-I Human chr11 - 3793059 3793059 3793059 TCGCCCAAGTCGGAGTGCAGTGGCGCTATCTCAGCGTACTCCAACCTCCGCCTCCCAGGTTCAAG TCGCCCAAGTCGGAGTGCAGTGGCGCTATCTCGGCGTACTCCAACCTCCGCCTCCCAGGTTCAAG T C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs896296405 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11615861 RMVar_hsa_circ_125448,RMVar_hsa_circ_147660,RMVar_hsa_circ_128055,RMVar_hsa_circ_147669,RMVar_hsa_circ_92246,RMVar_hsa_circ_147707 4363 RMVar_ID_4363 Human_SNP_ID_453934280 A-to-I Human chr11 - 3793395 3793371 3793396 TAGTCCCAGCTACTGGGAGGCTGAGGCAGAGAATCGCTTGAACCCAGGAGGCAGAGGTTGCAGTG TAGTCCCAGCTACTGGGAGGCTGAGGCAGAG_________________________GTTGCAGTG CCTCTGCCTCCTGGGTTCAAGCGATT C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1171605980 Functional Loss DEL dbSNP153 32..56 33 - - - Human_RBP_ID_11615870 RMVar_hsa_circ_125448,RMVar_hsa_circ_147660,RMVar_hsa_circ_128055,RMVar_hsa_circ_147669,RMVar_hsa_circ_92246,RMVar_hsa_circ_147707 4364 RMVar_ID_4364 Human_SNP_ID_453934295 A-to-I Human chr11 - 3793416 3793416 3793416 GGGCACAGTGACACGCACCTGTAGTCCCAGCTACTGGGAGGCTGAGGCAGAGAATCGCTTGAACC GGGCACAGTGACACGCACCTGTAGTCCCAGCTGCTGGGAGGCTGAGGCAGAGAATCGCTTGAACC T C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs952266872 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125448,RMVar_hsa_circ_147660,RMVar_hsa_circ_128055,RMVar_hsa_circ_147669,RMVar_hsa_circ_92246,RMVar_hsa_circ_147707 4365 RMVar_ID_4365 Human_SNP_ID_453934307 A-to-I Human chr11 - 3793452 3793452 3793452 GAAACCCTGAATCTACTAAAAATAGAAAAATTAGTTGGGCACAGTGACACGCACCTGTAGTCCCA GAAACCCTGAATCTACTAAAAATAGAAAAATTTGTTGGGCACAGTGACACGCACCTGTAGTCCCA T A NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1174294283 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11615871 RMVar_hsa_circ_125448,RMVar_hsa_circ_147660,RMVar_hsa_circ_128055,RMVar_hsa_circ_147669,RMVar_hsa_circ_92246,RMVar_hsa_circ_147707 4366 RMVar_ID_4366 Human_SNP_ID_453934721 A-to-I Human chr11 - 3794677 3794677 3794677 CTGGAAGATTGAGACTGCAGTGCTGTGATTGCACCACTGCTTTCCAGCCTGGGAAACTGCGTGAG CTGGAAGATTGAGACTGCAGTGCTGTGATTGCGCCACTGCTTTCCAGCCTGGGAAACTGCGTGAG T C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1054357443 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11615901 RMVar_hsa_circ_125448,RMVar_hsa_circ_147660,RMVar_hsa_circ_128055,RMVar_hsa_circ_147669,RMVar_hsa_circ_92246,RMVar_hsa_circ_147707 4367 RMVar_ID_4367 Human_SNP_ID_453936197 A-to-I Human chr11 + 3798823 3798823 3798823 TCGCCGCCGCGCCCAGCTGATTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGC TCGCCGCCGCGCCCAGCTGATTTTGTATTTTTGGTAGAGATGGGGTTTCACCATGTTGGCCAGGC A G PGAP2 Ensembl:ENSG00000148985 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909243551 Functional Loss SNV dbSNP153 33..33 33 - - - 4368 RMVar_ID_4368 Human_SNP_ID_453936218 A-to-I Human chr11 + 3798877 3798877 3798877 GTTGGCCAGGCTGGTCTCGAACTCCGGAACTCAGGTGATCCGCCCGCCTCGGCCTCCCACAGTGC GTTGGCCAGGCTGGTCTCGAACTCCGGAACTCGGGTGATCCGCCCGCCTCGGCCTCCCACAGTGC A G PGAP2 Ensembl:ENSG00000148985 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053430788 Functional Loss SNV dbSNP153 33..33 33 - - - 4369 RMVar_ID_4369 Human_SNP_ID_453936373 A-to-I Human chr11 + 3799480 3799480 3799480 CGAGAATGGCTTGAACCAGGGAGGCGGAGATTACAGTGAGTGGAGATCCTGCCACTGCGCTCCAG CGAGAATGGCTTGAACCAGGGAGGCGGAGATTGCAGTGAGTGGAGATCCTGCCACTGCGCTCCAG A G PGAP2 Ensembl:ENSG00000148985 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1038205537 Functional Loss SNV dbSNP153 33..33 33 - - - 4370 RMVar_ID_4370 Human_SNP_ID_453936473 A-to-I Human chr11 + 3799856 3799856 3799856 AGGTGTGGTGGCAAGCGCCTGTGGTCCCAGCTACTAGGGAGGCTGAAGTAGGAGGATCGTTTGAG AGGTGTGGTGGCAAGCGCCTGTGGTCCCAGCTGCTAGGGAGGCTGAAGTAGGAGGATCGTTTGAG A G PGAP2 Ensembl:ENSG00000148985 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs748343842 Functional Loss SNV dbSNP153 33..33 33 - - - 4371 RMVar_ID_4371 Human_SNP_ID_453936476 A-to-I Human chr11 + 3799859 3799859 3799859 TGTGGTGGCAAGCGCCTGTGGTCCCAGCTACTAGGGAGGCTGAAGTAGGAGGATCGTTTGAGCCC TGTGGTGGCAAGCGCCTGTGGTCCCAGCTACTGGGGAGGCTGAAGTAGGAGGATCGTTTGAGCCC A G PGAP2 Ensembl:ENSG00000148985 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1271834585 Functional Loss SNV dbSNP153 33..33 33 - - - 4372 RMVar_ID_4372 Human_SNP_ID_453938273 A-to-I Human chr11 + 3805932 3805932 3805932 TTGTCTCGATCTCTTGACCTTGTGATCCGCCCACCTTGGCCTCCCAAAGTGCTGGGATTACAGAT TTGTCTCGATCTCTTGACCTTGTGATCCGCCCCCCTTGGCCTCCCAAAGTGCTGGGATTACAGAT A C PGAP2 Ensembl:ENSG00000148985 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1023833322 Functional Loss SNV dbSNP153 33..33 33 - - - 4373 RMVar_ID_4373 Human_SNP_ID_453939693 A-to-I Human chr11 + 3811651 3811651 3811651 GTCACTGAAGTGTAATATAGAGTCAGTAAATGAATTACAAGTATAACAGAGTTTGACACATGTCC GTCACTGAAGTGTAATATAGAGTCAGTAAATGCATTACAAGTATAACAGAGTTTGACACATGTCC A C PGAP2 Ensembl:ENSG00000148985 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs943205372 Functional Loss SNV dbSNP153 33..33 33 - - - 4374 RMVar_ID_4374 Human_SNP_ID_453939694 A-to-I Human chr11 + 3811655 3811655 3811655 CTGAAGTGTAATATAGAGTCAGTAAATGAATTACAAGTATAACAGAGTTTGACACATGTCCCACC CTGAAGTGTAATATAGAGTCAGTAAATGAATTGCAAGTATAACAGAGTTTGACACATGTCCCACC A G PGAP2 Ensembl:ENSG00000148985 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs575279313 Functional Loss SNV dbSNP153 33..33 33 - - - 4375 RMVar_ID_4375 Human_SNP_ID_453939700 A-to-I Human chr11 + 3811666 3811666 3811666 TATAGAGTCAGTAAATGAATTACAAGTATAACAGAGTTTGACACATGTCCCACCCCATTTACTTT TATAGAGTCAGTAAATGAATTACAAGTATAACGGAGTTTGACACATGTCCCACCCCATTTACTTT A G PGAP2 Ensembl:ENSG00000148985 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs929390688 Functional Loss SNV dbSNP153 33..33 33 - - - 4376 RMVar_ID_4376 Human_SNP_ID_453939705 A-to-I Human chr11 + 3811678 3811678 3811678 AAATGAATTACAAGTATAACAGAGTTTGACACATGTCCCACCCCATTTACTTTGATATCCTAGAG AAATGAATTACAAGTATAACAGAGTTTGACACGTGTCCCACCCCATTTACTTTGATATCCTAGAG A G PGAP2 Ensembl:ENSG00000148985 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs949182921 Functional Loss SNV dbSNP153 33..33 33 - - - 4377 RMVar_ID_4377 Human_SNP_ID_453939800 A-to-I Human chr11 + 3812163 3812163 3812163 AAAGATGTAAGACCACTTTCTCTAGGATATCAAAGTAAGTGGGGTGGGACATATGTCAAACTCTG AAAGATGTAAGACCACTTTCTCTAGGATATCAGAGTAAGTGGGGTGGGACATATGTCAAACTCTG A G PGAP2 Ensembl:ENSG00000148985 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs942631912 Functional Loss SNV dbSNP153 33..33 33 - - - 4378 RMVar_ID_4378 Human_SNP_ID_453939809 A-to-I Human chr11 + 3812200 3812200 3812200 AGTGGGGTGGGACATATGTCAAACTCTGTTATACTTGTAATTCATTTACTGACTCTATATTACCT AGTGGGGTGGGACATATGTCAAACTCTGTTATGCTTGTAATTCATTTACTGACTCTATATTACCT A G PGAP2 Ensembl:ENSG00000148985 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1175140656 Functional Loss SNV dbSNP153 33..33 33 - - - 4379 RMVar_ID_4379 Human_SNP_ID_453939813 A-to-I Human chr11 + 3812215 3812215 3812215 ATGTCAAACTCTGTTATACTTGTAATTCATTTACTGACTCTATATTACCTGAGACAGAGACCCAG ATGTCAAACTCTGTTATACTTGTAATTCATTTGCTGACTCTATATTACCTGAGACAGAGACCCAG A G PGAP2 Ensembl:ENSG00000148985 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879290718 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23504574 4380 RMVar_ID_4380 Human_SNP_ID_453939840 A-to-I Human chr11 + 3812354 3812354 3812354 AGGAGCCTGAGGTGGGAGGATTGCTTGAGCCTAGAAGTCTGAGGCTGGAGTGAGCTATGGTTTTC AGGAGCCTGAGGTGGGAGGATTGCTTGAGCCTGGAAGTCTGAGGCTGGAGTGAGCTATGGTTTTC A G PGAP2 Ensembl:ENSG00000148985 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs890230475 Functional Loss SNV dbSNP153 33..33 33 - - - 4381 RMVar_ID_4381 Human_SNP_ID_453939849 A-to-I Human chr11 + 3812412 3812412 3812412 GGTTTTCTCACTGTACTTCAGCCTGATGACATAGTGAGACCCCCATTTCTAAAAAATAAAATAGG GGTTTTCTCACTGTACTTCAGCCTGATGACATGGTGAGACCCCCATTTCTAAAAAATAAAATAGG A G PGAP2 Ensembl:ENSG00000148985 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1190476524 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23504576 4382 RMVar_ID_4382 Human_SNP_ID_453939866 A-to-I Human chr11 + 3812492 3812492 3812492 CCTGCTCCTTCCCAGGGCTAGTGTAGAGCTCTAGGTAGAAGAAGGATAGGAAGGTAGTTTAGGGA CCTGCTCCTTCCCAGGGCTAGTGTAGAGCTCTCGGTAGAAGAAGGATAGGAAGGTAGTTTAGGGA A C PGAP2 Ensembl:ENSG00000148985 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1384226339 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23504578 4383 RMVar_ID_4383 Human_SNP_ID_453940033 A-to-I Human chr11 + 3813232 3813232 3813232 TGAGAAAGTATTTGGGTTTTTTTATTTGTTTTAGAGGCAGGGTCTCATTTCCGTCACCCAGGCCA TGAGAAAGTATTTGGGTTTTTTTATTTGTTTTGGAGGCAGGGTCTCATTTCCGTCACCCAGGCCA A G PGAP2 Ensembl:ENSG00000148985 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs920674281 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6073032,Human_RBP_ID_11616045 4384 RMVar_ID_4384 Human_SNP_ID_453940034 A-to-I Human chr11 + 3813232 3813232 3813232 TGAGAAAGTATTTGGGTTTTTTTATTTGTTTTAGAGGCAGGGTCTCATTTCCGTCACCCAGGCCA TGAGAAAGTATTTGGGTTTTTTTATTTGTTTTTGAGGCAGGGTCTCATTTCCGTCACCCAGGCCA A T PGAP2 Ensembl:ENSG00000148985 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs920674281 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6073032,Human_RBP_ID_11616045 4385 RMVar_ID_4385 Human_SNP_ID_453940349 A-to-I Human chr11 + 3814681 3814681 3814681 GTGATCCTCCTGCCTCAGCCTTCCAGAGTGCTAGGATTACAGGCTTGAGCCACTGTGCCTAGCCC GTGATCCTCCTGCCTCAGCCTTCCAGAGTGCTGGGATTACAGGCTTGAGCCACTGTGCCTAGCCC A G PGAP2 Ensembl:ENSG00000148985 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1488663303 Functional Loss SNV dbSNP153 33..33 33 - - - 4386 RMVar_ID_4386 Human_SNP_ID_453940782 A-to-I Human chr11 + 3815438 3815438 3815438 TCAAGCGATTCTCCTGTCTCAGCCTCCCGAGTAGCTGGGATTACAGGCACACCGCCACCATGACT TCAAGCGATTCTCCTGTCTCAGCCTCCCGAGTGGCTGGGATTACAGGCACACCGCCACCATGACT A G PGAP2 Ensembl:ENSG00000148985 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928009292 Functional Loss SNV dbSNP153 33..33 33 - - - 4387 RMVar_ID_4387 Human_SNP_ID_453940783 A-to-I Human chr11 + 3815448 3815444 3815449 CTCCTGTCTCAGCCTCCCGAGTAGCTGGGATTACAGGCACACCGCCACCATGACTGGCTAACTTT CTCCTGTCTCAGCCTCCCGAGTAGCTGGG_____AGGCACACCGCCACCATGACTGGCTAACTTT GATTAC G PGAP2 Ensembl:ENSG00000148985 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1214642040 Functional Loss DEL dbSNP153 30..34 33 - - - 4388 RMVar_ID_4388 Human_SNP_ID_453940784 A-to-I Human chr11 + 3815448 3815448 3815448 CTCCTGTCTCAGCCTCCCGAGTAGCTGGGATTACAGGCACACCGCCACCATGACTGGCTAACTTT CTCCTGTCTCAGCCTCCCGAGTAGCTGGGATTCCAGGCACACCGCCACCATGACTGGCTAACTTT A C PGAP2 Ensembl:ENSG00000148985 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1252785315 Functional Loss SNV dbSNP153 33..33 33 - - - 4389 RMVar_ID_4389 Human_SNP_ID_453941409 A-to-I Human chr11 + 3817857 3817857 3817857 TCACTCGAGTTCAGTTCGAGACCAGCCTGGGCAACATGGTGAAACCCCGTCTGTACAAAAAATGC TCACTCGAGTTCAGTTCGAGACCAGCCTGGGCGACATGGTGAAACCCCGTCTGTACAAAAAATGC A G PGAP2 Ensembl:ENSG00000148985 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs954501263 Functional Loss SNV dbSNP153 33..33 33 - - - 4390 RMVar_ID_4390 Human_SNP_ID_453941443 A-to-I Human chr11 + 3817925 3817925 3817925 AAAATTAGCTGGGTGCCCTGGCATGCCCCTGTAGTCCCAGCTACTTGGGAGGCTAAGGCAGGAGA AAAATTAGCTGGGTGCCCTGGCATGCCCCTGTGGTCCCAGCTACTTGGGAGGCTAAGGCAGGAGA A G PGAP2 Ensembl:ENSG00000148985 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1180095434 Functional Loss SNV dbSNP153 33..33 33 - - - 4391 RMVar_ID_4391 Human_SNP_ID_453941762 A-to-I Human chr11 + 3819080 3819080 3819080 TTACATATTTATTTATTTAGAGACAGGATCTCACTCTGTCTCCCAGGCGGGAGTACAGTGACCTG TTACATATTTATTTATTTAGAGACAGGATCTCGCTCTGTCTCCCAGGCGGGAGTACAGTGACCTG A G PGAP2 Ensembl:ENSG00000148985 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459473477 Functional Loss SNV dbSNP153 33..33 33 - - - 4392 RMVar_ID_4392 Human_SNP_ID_453941793 A-to-I Human chr11 + 3819191 3819191 3819191 CGCCTCAGCCTCAGCCTTGGGTAGCTGGGACTACAGGTGCATGCCACCATGCCTGGCTAATTCTT CGCCTCAGCCTCAGCCTTGGGTAGCTGGGACTGCAGGTGCATGCCACCATGCCTGGCTAATTCTT A G PGAP2 Ensembl:ENSG00000148985 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs542360832 Functional Loss SNV dbSNP153 33..33 33 - - - 4393 RMVar_ID_4393 Human_SNP_ID_453942093 A-to-I Human chr11 + 3820566 3820566 3820566 TCTGTAATCCCAGCTACTCGGGAGACTGAGGCAGGAGAATTGCTTGAACCTGGGAGGTGGAGTTT TCTGTAATCCCAGCTACTCGGGAGACTGAGGCGGGAGAATTGCTTGAACCTGGGAGGTGGAGTTT A G PGAP2 Ensembl:ENSG00000148985 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048528742 Functional Loss SNV dbSNP153 33..33 33 - - - 4394 RMVar_ID_4394 Human_SNP_ID_453942180 A-to-I Human chr11 + 3820889 3820889 3820889 CCCTGCAAGGTAGGTGGTGTTATACCCATTTTACCAATGAGGAAATTGGAGCTCAGAGAGGTGAA CCCTGCAAGGTAGGTGGTGTTATACCCATTTTGCCAATGAGGAAATTGGAGCTCAGAGAGGTGAA A G PGAP2 Ensembl:ENSG00000148985 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs894168417 Functional Loss SNV dbSNP153 33..33 33 - - - 4395 RMVar_ID_4395 Human_SNP_ID_453942699 A-to-I Human chr11 + 3822609 3822609 3822609 TGAGTCATGATCATGCTATTGCACTCCAGCCTAGGCGACAGAGTGAGACCCTGTCTCAAAAAGGG TGAGTCATGATCATGCTATTGCACTCCAGCCTGGGCGACAGAGTGAGACCCTGTCTCAAAAAGGG A G PGAP2 Ensembl:ENSG00000148985 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1326681004 Functional Loss SNV dbSNP153 33..33 33 - - - 4396 RMVar_ID_4396 Human_SNP_ID_453943951 A-to-I Human chr11 - 3826263 3826262 3826263 GGTTTGGAGCAGTAGGGAAGACAGGAGATACCAGGGAGCCCATTTTACAGTAGAGATCTGCATCT GGTTTGGAGCAGTAGGGAAGACAGGAGATACC_GGGAGCCCATTTTACAGTAGAGATCTGCATCT CT C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1168132532 Functional Loss DEL dbSNP153 33..33 33 - - - 4397 RMVar_ID_4397 Human_SNP_ID_453967507 A-to-I Human chr11 + 3915846 3915846 3915846 GGGAGGCTGAGGTGGGCAGATCACTTCAGGTCAGGAGTTTGGGACCAGCCTGGCCAACATGGCAA GGGAGGCTGAGGTGGGCAGATCACTTCAGGTCGGGAGTTTGGGACCAGCCTGGCCAACATGGCAA A G STIM1 Ensembl:ENSG00000167323 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1409603250 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104299,RMVar_hsa_circ_147736 4398 RMVar_ID_4398 Human_SNP_ID_453967985 A-to-I Human chr11 + 3917635 3917635 3917635 TTTTGCATTTTTTGTAGAGACAGGATTTTGCCATGTTGCCCAGGCTGGTGTTGAACTCCTGGACT TTTTGCATTTTTTGTAGAGACAGGATTTTGCCGTGTTGCCCAGGCTGGTGTTGAACTCCTGGACT A G STIM1 Ensembl:ENSG00000167323 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167924934 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104299,RMVar_hsa_circ_147736 4399 RMVar_ID_4399 Human_SNP_ID_453968112 A-to-I Human chr11 + 3918259 3918259 3918259 ATACAACAGGCCTGGCATGTTGGTTCAAGCCTATAATTCTAGCATTTTGGGAGGCCAAGGCAGGT ATACAACAGGCCTGGCATGTTGGTTCAAGCCTGTAATTCTAGCATTTTGGGAGGCCAAGGCAGGT A G STIM1 Ensembl:ENSG00000167323 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417015436 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104299,RMVar_hsa_circ_147736 4400 RMVar_ID_4400 Human_SNP_ID_453973733 A-to-I Human chr11 - 3942204 3942200 3942205 CAGACCAGGTTGAAGTCCTGGTTTGGCTACTAACTCGATCACACACCATATCCATTCTTACCTCC CAGACCAGGTTGAAGTCCTGGTTTGGCTACT_____GATCACACACCATATCCATTCTTACCTCC CGAGTT C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1276038198 Functional Loss DEL dbSNP153 32..36 33 - - - 4401 RMVar_ID_4401 Human_SNP_ID_453973733 A-to-I Human chr11 - 3942205 3942200 3942205 ACAGACCAGGTTGAAGTCCTGGTTTGGCTACTAACTCGATCACACACCATATCCATTCTTACCTC ACAGACCAGGTTGAAGTCCTGGTTTGGCTACT_____GATCACACACCATATCCATTCTTACCTC CGAGTT C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1276038198 Functional Loss DEL dbSNP153 33..37 33 - - - 4402 RMVar_ID_4402 Human_SNP_ID_453973737 A-to-I Human chr11 - 3942208 3942203 3942209 TAGACAGACCAGGTTGAAGTCCTGGTTTGGCTACTAACTCGATCACACACCATATCCATTCTTAC TAGACAGACCAGGTTGAAGTCCTGGTTTGGC______CTCGATCACACACCATATCCATTCTTAC GTTAGTA G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1247103784 Functional Loss DEL dbSNP153 32..37 33 - - - 4403 RMVar_ID_4403 Human_SNP_ID_453984571 A-to-I Human chr11 - 3991316 3991316 3991316 ACAATACAAAGAAATTAGCCAGGCAGTGGTGCATGCCTGTAGTTCCAGCTACTCAGAAGCTGAGG ACAATACAAAGAAATTAGCCAGGCAGTGGTGCGTGCCTGTAGTTCCAGCTACTCAGAAGCTGAGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs977445735 Functional Loss SNV dbSNP153 33..33 33 - - - 4404 RMVar_ID_4404 Human_SNP_ID_453984628 A-to-I Human chr11 - 3991566 3991566 3991566 GTATACATACCCAAAGGAAAATAAATTATTCTACTAAAAAGACATGTGCACTCATATGTTCACTG GTATACATACCCAAAGGAAAATAAATTATTCTGCTAAAAAGACATGTGCACTCATATGTTCACTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924286119 Functional Loss SNV dbSNP153 33..33 33 - - - 4405 RMVar_ID_4405 Human_SNP_ID_454006153 A-to-I Human chr11 + 4079431 4079431 4079431 CCCCGTCTCTACTAAAAATACAAGAATTAGCCAGGTGTGGTGGCAGGCACCTGTAATCACAGCTA CCCCGTCTCTACTAAAAATACAAGAATTAGCCGGGTGTGGTGGCAGGCACCTGTAATCACAGCTA A G STIM1 Ensembl:ENSG00000167323 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs752196642 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104299,RMVar_hsa_circ_147736,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 4406 RMVar_ID_4406 Human_SNP_ID_454010297 A-to-I Human chr11 + 4096049 4096048 4096050 GAACATTTCAAAGATGGAGACTTGTTTGAGACAGAGTCTTGCTCTGTCACCCAGGATGGAATGCA GAACATTTCAAAGATGGAGACTTGTTTGAGAC__AGTCTTGCTCTGTCACCCAGGATGGAATGCA CAG C RRM1 Ensembl:ENSG00000167325 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1183955854 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_11616929 RMVar_hsa_circ_147761,RMVar_hsa_circ_127669 4407 RMVar_ID_4407 Human_SNP_ID_454010343 A-to-I Human chr11 + 4096214 4096214 4096214 TGAGTGGCTAATTTTTAAAAATTTCTGGTAGTAAAGGAGTCTTGCTGTGTTTCCCAGTCTGGCCT TGAGTGGCTAATTTTTAAAAATTTCTGGTAGTGAAGGAGTCTTGCTGTGTTTCCCAGTCTGGCCT A G RRM1 Ensembl:ENSG00000167325 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1361499511 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11616932,Human_RBP_ID_22161549 RMVar_hsa_circ_147761,RMVar_hsa_circ_127669 4408 RMVar_ID_4408 Human_SNP_ID_454010549 A-to-I Human chr11 + 4097149 4097149 4097149 TCTACTAAAAACACAAAAGTTAGCCGGACGGTAGTGGTTTGCACCTGTAATCCCAGCTACTCAGG TCTACTAAAAACACAAAAGTTAGCCGGACGGTTGTGGTTTGCACCTGTAATCCCAGCTACTCAGG A T RRM1 Ensembl:ENSG00000167325 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs184178991 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1161977,Human_RBP_ID_11616971 RMVar_hsa_circ_147761,RMVar_hsa_circ_127669 4409 RMVar_ID_4409 Human_SNP_ID_454014378 A-to-I Human chr11 + 4112387 4112386 4112388 ATTATATTCCTTTTTTTTTTTGTTGTTGAGACAAAGTCTCACTCTGTCACCCAGGCTGGAGCGCA ATTATATTCCTTTTTTTTTTTGTTGTTGAGAC__AGTCTCACTCTGTCACCCAGGCTGGAGCGCA CAA C RRM1 Ensembl:ENSG00000167325 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs377371904 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_341423,RMVar_hsa_circ_349916,RMVar_hsa_circ_363370,RMVar_hsa_circ_4282,RMVar_hsa_circ_18840,RMVar_hsa_circ_100738,RMVar_hsa_circ_147768,RMVar_hsa_circ_36523,RMVar_hsa_circ_43661,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 4410 RMVar_ID_4410 Human_SNP_ID_454014378 A-to-I Human chr11 + 4112388 4112386 4112388 TTATATTCCTTTTTTTTTTTGTTGTTGAGACAAAGTCTCACTCTGTCACCCAGGCTGGAGCGCAG TTATATTCCTTTTTTTTTTTGTTGTTGAGAC__AGTCTCACTCTGTCACCCAGGCTGGAGCGCAG CAA C RRM1 Ensembl:ENSG00000167325 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs377371904 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_341423,RMVar_hsa_circ_349916,RMVar_hsa_circ_363370,RMVar_hsa_circ_4282,RMVar_hsa_circ_18840,RMVar_hsa_circ_100738,RMVar_hsa_circ_147768,RMVar_hsa_circ_36523,RMVar_hsa_circ_43661,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 4411 RMVar_ID_4411 Human_SNP_ID_454014379 A-to-I Human chr11 + 4112387 4112387 4112387 ATTATATTCCTTTTTTTTTTTGTTGTTGAGACAAAGTCTCACTCTGTCACCCAGGCTGGAGCGCA ATTATATTCCTTTTTTTTTTTGTTGTTGAGACGAAGTCTCACTCTGTCACCCAGGCTGGAGCGCA A G RRM1 Ensembl:ENSG00000167325 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1192750234 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_341423,RMVar_hsa_circ_349916,RMVar_hsa_circ_363370,RMVar_hsa_circ_4282,RMVar_hsa_circ_18840,RMVar_hsa_circ_100738,RMVar_hsa_circ_147768,RMVar_hsa_circ_36523,RMVar_hsa_circ_43661,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 4412 RMVar_ID_4412 Human_SNP_ID_454014918 A-to-I Human chr11 + 4114812 4114812 4114812 TTGGCTTACTGCAGCCTGCACCTCCCAGGTCCAAGTGATTCTCCTGCCTCAGCTTTACAAATAGT TTGGCTTACTGCAGCCTGCACCTCCCAGGTCCGAGTGATTCTCCTGCCTCAGCTTTACAAATAGT A G RRM1 Ensembl:ENSG00000167325 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1008587185 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_341423,RMVar_hsa_circ_349916,RMVar_hsa_circ_363370,RMVar_hsa_circ_4282,RMVar_hsa_circ_18840,RMVar_hsa_circ_100738,RMVar_hsa_circ_147768,RMVar_hsa_circ_36523,RMVar_hsa_circ_43661,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 4413 RMVar_ID_4413 Human_SNP_ID_454015383 A-to-I Human chr11 + 4116445 4116445 4116445 GAAACCCTGTCTTTACTAAAAATACAACTATTAGCCAGGCGTGGTGGCGTATGCCCATAATCCCA GAAACCCTGTCTTTACTAAAAATACAACTATTGGCCAGGCGTGGTGGCGTATGCCCATAATCCCA A G RRM1 Ensembl:ENSG00000167325 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404931101 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_341423,RMVar_hsa_circ_349916,RMVar_hsa_circ_363370,RMVar_hsa_circ_4282,RMVar_hsa_circ_18840,RMVar_hsa_circ_100738,RMVar_hsa_circ_147768,RMVar_hsa_circ_36523,RMVar_hsa_circ_43661,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 4414 RMVar_ID_4414 Human_SNP_ID_454019830 A-to-I Human chr11 + 4135214 4135214 4135214 TCATTGATCAAAGCCAATCTTTGAACATCCACATTGCTGAGCCTAACTATGGCAAACTCACTAGT TCATTGATCAAAGCCAATCTTTGAACATCCACGTTGCTGAGCCTAACTATGGCAAACTCACTAGT A G RRM1 Ensembl:ENSG00000167325 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1262415615 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1779179,Human_RBP_ID_17804897,Human_RBP_ID_26803156 Human_Splice_Rec_1202615,Human_Splice_Rec_1202651,Human_Splice_Rec_1202691,Human_Splice_Rec_1202733,Human_Splice_Rec_1202757 Human_miRNA_ID_676124,Human_miRNA_ID_732426,Human_miRNA_ID_2269530 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 4415 RMVar_ID_4415 Human_SNP_ID_454478507 A-to-I Human chr11 - 5668179 5668179 5668179 CCTCAGTCAAACTTCTGGGCTCAAATTCTCCCACCTCATCTTCCCAAGTAGTTGGAACTACAGGC CCTCAGTCAAACTTCTGGGCTCAAATTCTCCCGCCTCATCTTCCCAAGTAGTTGGAACTACAGGC T C AC104389.5,TRIM5 Ensembl:ENSG00000239920,Ensembl:ENSG00000132256 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1407697206 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55841 4416 RMVar_ID_4416 Human_SNP_ID_454479002 A-to-I Human chr11 - 5669892 5669892 5669892 TGGATAACTGCAACCTCCGCCTCCTGGGTTCAAACAATTCTTGTGCCTCAGCCGCCTGAGTAGCT TGGATAACTGCAACCTCCGCCTCCTGGGTTCACACAATTCTTGTGCCTCAGCCGCCTGAGTAGCT T G AC104389.5,TRIM5 Ensembl:ENSG00000239920,Ensembl:ENSG00000132256 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1040588583 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55841 4417 RMVar_ID_4417 Human_SNP_ID_454479008 A-to-I Human chr11 - 5669912 5669912 5669912 GGAGTGCAGTGGTGTGATCTTGGATAACTGCAACCTCCGCCTCCTGGGTTCAAACAATTCTTGTG GGAGTGCAGTGGTGTGATCTTGGATAACTGCACCCTCCGCCTCCTGGGTTCAAACAATTCTTGTG T G AC104389.5,TRIM5 Ensembl:ENSG00000239920,Ensembl:ENSG00000132256 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1004426859 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55841 4418 RMVar_ID_4418 Human_SNP_ID_454479186 A-to-I Human chr11 - 5670306 5670306 5670306 GGGTGTGGTGGTGGGAGCCTGTAGTCCCAGCTACTCGGGAGGCTGAAACAGGAGAATGGCATGAA GGGTGTGGTGGTGGGAGCCTGTAGTCCCAGCTGCTCGGGAGGCTGAAACAGGAGAATGGCATGAA T C AC104389.5,TRIM5 Ensembl:ENSG00000239920,Ensembl:ENSG00000132256 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1029139925 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55841 4419 RMVar_ID_4419 Human_SNP_ID_454479191 A-to-I Human chr11 - 5670316 5670316 5670316 AAAATTAGCTGGGTGTGGTGGTGGGAGCCTGTAGTCCCAGCTACTCGGGAGGCTGAAACAGGAGA AAAATTAGCTGGGTGTGGTGGTGGGAGCCTGTGGTCCCAGCTACTCGGGAGGCTGAAACAGGAGA T C AC104389.5,TRIM5 Ensembl:ENSG00000239920,Ensembl:ENSG00000132256 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1298037528 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55841 4420 RMVar_ID_4420 Human_SNP_ID_454479395 A-to-I Human chr11 - 5671043 5671043 5671043 TTTTGTATTTTTTGTAGAGATGGGATTTCACCATGTTGCCCAGGCTGGTCTCAATCCACTTGCCT TTTTGTATTTTTTGTAGAGATGGGATTTCACCGTGTTGCCCAGGCTGGTCTCAATCCACTTGCCT T C AC104389.5,TRIM5 Ensembl:ENSG00000239920,Ensembl:ENSG00000132256 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs996634572 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55841 4421 RMVar_ID_4421 Human_SNP_ID_454479401 A-to-I Human chr11 - 5671078 5671078 5671078 GGGACTACAGCTCCGCACTACCATGCTCACCTAATTTTTGTATTTTTTGTAGAGATGGGATTTCA GGGACTACAGCTCCGCACTACCATGCTCACCTGATTTTTGTATTTTTTGTAGAGATGGGATTTCA T C AC104389.5,TRIM5 Ensembl:ENSG00000239920,Ensembl:ENSG00000132256 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1159776883 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55841 4422 RMVar_ID_4422 Human_SNP_ID_454479420 A-to-I Human chr11 - 5671143 5671143 5671143 TGACTCACTATAGCCTCGACATCCTGAACTCAAGCAATCCCCTCACCTCAGACCCCAGACTAGCT TGACTCACTATAGCCTCGACATCCTGAACTCAGGCAATCCCCTCACCTCAGACCCCAGACTAGCT T C AC104389.5,TRIM5 Ensembl:ENSG00000239920,Ensembl:ENSG00000132256 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285385067 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55841 4423 RMVar_ID_4423 Human_SNP_ID_454479434 A-to-I Human chr11 - 5671195 5671195 5671195 TTTAGACAGAGTCTCACTCTGTTGCCCATGCTAGTATGTAGTGGTGCGATCTTGACTCACTATAG TTTAGACAGAGTCTCACTCTGTTGCCCATGCTGGTATGTAGTGGTGCGATCTTGACTCACTATAG T C AC104389.5,TRIM5 Ensembl:ENSG00000239920,Ensembl:ENSG00000132256 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1276298710 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55841 4424 RMVar_ID_4424 Human_SNP_ID_454656067 A-to-I Human chr11 - 6320345 6320345 6320345 TCCATGCTGGAGACTCTGCGGGAGCGGCAGGGAGGCCTGGCTCGAAGGCAGGGAGGCCTGGCAGG TCCATGCTGGAGACTCTGCGGGAGCGGCAGGGGGGCCTGGCTCGAAGGCAGGGAGGCCTGGCAGG T C CAVIN3 Ensembl:ENSG00000170955 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs745862233 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126440,RMVar_hsa_circ_147817 4425 RMVar_ID_4425 Human_SNP_ID_454656459 A-to-I Human chr11 + 6321532 6321532 6321532 CGGGCGCGGTGGCTCATGCTTGTAATCCCACCACTTTGGGAGGCCGAGGGGGGAGGATCACGTGA CGGGCGCGGTGGCTCATGCTTGTAATCCCACCCCTTTGGGAGGCCGAGGGGGGAGGATCACGTGA A C AC068733.3 Ensembl:ENSG00000282556 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1390573119 Functional Loss SNV dbSNP153 33..33 33 - - - 4426 RMVar_ID_4426 Human_SNP_ID_454656460 A-to-I Human chr11 + 6321532 6321532 6321532 CGGGCGCGGTGGCTCATGCTTGTAATCCCACCACTTTGGGAGGCCGAGGGGGGAGGATCACGTGA CGGGCGCGGTGGCTCATGCTTGTAATCCCACCGCTTTGGGAGGCCGAGGGGGGAGGATCACGTGA A G AC068733.3 Ensembl:ENSG00000282556 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1390573119 Functional Loss SNV dbSNP153 33..33 33 - - - 4427 RMVar_ID_4427 Human_SNP_ID_454700846 A-to-I Human chr11 + 6490968 6490968 6490968 GGGCGTGGTGGCACATGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGTGTGAGGATTGCTTGAT GGGCGTGGTGGCACATGCCTGTAGTCCCAGCTGCTTGGGAGGCTGAGGTGTGAGGATTGCTTGAT A G AC084337.2 Ensembl:ENSG00000283977 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs998799524 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11671233 4428 RMVar_ID_4428 Human_SNP_ID_454700869 A-to-I Human chr11 + 6491066 6491066 6491066 ACCTCACTGCCCTCCAGCCTGGGTGACAGAGCAAGACCCTGTCTCAAAATAATAAAATAAACCAG ACCTCACTGCCCTCCAGCCTGGGTGACAGAGCCAGACCCTGTCTCAAAATAATAAAATAAACCAG A C AC084337.2 Ensembl:ENSG00000283977 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs994886239 Functional Loss SNV dbSNP153 33..33 33 - - - 4429 RMVar_ID_4429 Human_SNP_ID_454701119 A-to-I Human chr11 + 6492148 6492138 6492148 GCATCGGGCCAGGTGCAGTGGTTCACACCTGTAATCCGAATGCTTTGGGAGGCCAAGATGGAAAG GCATCGGGCCAGGTGCAGTGGTT__________ATCCGAATGCTTTGGGAGGCCAAGATGGAAAG TCACACCTGTA T AC084337.2 Ensembl:ENSG00000283977 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs996455607 Functional Loss DEL dbSNP153 24..33 33 - - - 4430 RMVar_ID_4430 Human_SNP_ID_454701126 A-to-I Human chr11 + 6492170 6492170 6492170 TCACACCTGTAATCCGAATGCTTTGGGAGGCCAAGATGGAAAGATTGCTTGAGTTCAGGAGTTCA TCACACCTGTAATCCGAATGCTTTGGGAGGCCGAGATGGAAAGATTGCTTGAGTTCAGGAGTTCA A G AC084337.2 Ensembl:ENSG00000283977 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1327048863 Functional Loss SNV dbSNP153 33..33 33 - - - 4431 RMVar_ID_4431 Human_SNP_ID_454701270 A-to-I Human chr11 + 6492715 6492714 6492715 TGTGTTTTTTTGTTGTTTTTGTTTTTTGAGACAGGGTTTTGCTCTGTTGCCCAGGCTGGAGTGTG TGTGTTTTTTTGTTGTTTTTGTTTTTTGAGAC_GGGTTTTGCTCTGTTGCCCAGGCTGGAGTGTG CA C AC084337.2 Ensembl:ENSG00000283977 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1383787197 Functional Loss DEL dbSNP153 33..33 33 - - - 4432 RMVar_ID_4432 Human_SNP_ID_454701290 A-to-I Human chr11 + 6492818 6492818 6492818 GGCTCAAGTGATCCTTCCACCTCAGTCTCCCAAAGTTTTGGGATTACAGGAATGAGCCACCGCAC GGCTCAAGTGATCCTTCCACCTCAGTCTCCCACAGTTTTGGGATTACAGGAATGAGCCACCGCAC A C AC084337.2 Ensembl:ENSG00000283977 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs113542355 Functional Loss SNV dbSNP153 33..33 33 - - - 4433 RMVar_ID_4433 Human_SNP_ID_454711371 A-to-I Human chr11 + 6534795 6534795 6534795 ATTACCAAACAATGGAGACAGGATCTCAGGCTAGAGTGCAGTGTCATGATCACAGCTCACTGCAG ATTACCAAACAATGGAGACAGGATCTCAGGCTGGAGTGCAGTGTCATGATCACAGCTCACTGCAG A G DNHD1 Ensembl:ENSG00000179532 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1199105355 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_378069,RMVar_hsa_circ_56538,RMVar_hsa_circ_147836,RMVar_hsa_circ_102328,RMVar_hsa_circ_99440,RMVar_hsa_circ_147841,RMVar_hsa_circ_115665,RMVar_hsa_circ_147843,RMVar_hsa_circ_370979,RMVar_hsa_circ_119995,RMVar_hsa_circ_114950,RMVar_hsa_circ_147845,RMVar_hsa_circ_147846,RMVar_hsa_circ_147844,RMVar_hsa_circ_77621,RMVar_hsa_circ_118559,RMVar_hsa_circ_147848,RMVar_hsa_circ_147849,RMVar_hsa_circ_147850 4434 RMVar_ID_4434 Human_SNP_ID_454712759 A-to-I Human chr11 + 6540244 6540244 6540244 ATTAGTCTGTTCTGAGACAGTGTCTTCCATGTAGCCCCCCTACTGTCTTAATCTCCTTGGGATCC ATTAGTCTGTTCTGAGACAGTGTCTTCCATGTGGCCCCCCTACTGTCTTAATCTCCTTGGGATCC A G DNHD1 Ensembl:ENSG00000179532 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs943338035 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96013,RMVar_hsa_circ_378069,RMVar_hsa_circ_147836,RMVar_hsa_circ_102328,RMVar_hsa_circ_99440,RMVar_hsa_circ_147841,RMVar_hsa_circ_115665,RMVar_hsa_circ_147845,RMVar_hsa_circ_147844,RMVar_hsa_circ_77621,RMVar_hsa_circ_118559,RMVar_hsa_circ_147849,RMVar_hsa_circ_126107,RMVar_hsa_circ_147850,RMVar_hsa_circ_105518,RMVar_hsa_circ_147853,RMVar_hsa_circ_90290,RMVar_hsa_circ_147854,RMVar_hsa_circ_147855,RMVar_hsa_circ_147852,RMVar_hsa_circ_127288,RMVar_hsa_circ_105087,RMVar_hsa_circ_110667,RMVar_hsa_circ_88054,RMVar_hsa_circ_147858,RMVar_hsa_circ_147859,RMVar_hsa_circ_147856,RMVar_hsa_circ_147857 4435 RMVar_ID_4435 Human_SNP_ID_455102947 A-to-I Human chr11 - 8001578 8001578 8001578 TGGCTTTTTTCACTTACTCTTTATCCATATTGATATATAGAGGACTGTCTCATTCTGCTTAACAG TGGCTTTTTTCACTTACTCTTTATCCATATTGGTATATAGAGGACTGTCTCATTCTGCTTAACAG T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs550589581 Functional Loss SNV dbSNP153 33..33 33 - - - 4436 RMVar_ID_4436 Human_SNP_ID_455262555 A-to-I Human chr11 - 8614325 8614321 8614325 TTTATTTTTTATTTTTTGAGAGAGAGAGTCTCACTCTGTCATGCAGGCTGGAGTGCAGTGGTATG TTTATTTTTTATTTTTTGAGAGAGAGAGTCTC____TGTCATGCAGGCTGGAGTGCAGTGGTATG AGAGT A TRIM66 Ensembl:ENSG00000166436 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs757363818 Functional Loss DEL dbSNP153 33..36 33 - - - 4437 RMVar_ID_4437 Human_SNP_ID_455267319 A-to-I Human chr11 - 8632294 8632294 8632294 ATTTATTTATTTATTTTTTGAGATGAAATCTCACTCTGCCACCCAGGTTGGAGTGCAGTGGCATG ATTTATTTATTTATTTTTTGAGATGAAATCTCCCTCTGCCACCCAGGTTGGAGTGCAGTGGCATG T G TRIM66 Ensembl:ENSG00000166436 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1425070077 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27351 4438 RMVar_ID_4438 Human_SNP_ID_455267400 A-to-I Human chr11 - 8632532 8632532 8632532 AATCACTTGAACTTAGGAGGTGGAGAGGTTACAGTGAGCTGAGATCGTCTGACTGCACCCCAGCC AATCACTTGAACTTAGGAGGTGGAGAGGTTACGGTGAGCTGAGATCGTCTGACTGCACCCCAGCC T C TRIM66 Ensembl:ENSG00000166436 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs987499828 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27351 4439 RMVar_ID_4439 Human_SNP_ID_455273166 A-to-I Human chr11 - 8655578 8655578 8655578 GGGTTTTTCTATGTTGACCAAGCTGGTCTCGAACTCCTGACCTCAGGTGATCCTCCTGCCTTGGC GGGTTTTTCTATGTTGACCAAGCTGGTCTCGAGCTCCTGACCTCAGGTGATCCTCCTGCCTTGGC T C TRIM66 Ensembl:ENSG00000166436 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1186377542 Functional Loss SNV dbSNP153 33..33 33 - - - 4440 RMVar_ID_4440 Human_SNP_ID_455276640 A-to-I Human chr11 - 8669542 8669542 8669542 GCCTCCTGGGTTCAAGTGATTCTCCTGCGTCAACCTCCCAAATACCTGGGACTACAGCATGTGCC GCCTCCTGGGTTCAAGTGATTCTCCTGCGTCAGCCTCCCAAATACCTGGGACTACAGCATGTGCC T C TRIM66 Ensembl:ENSG00000166436 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904766267 Functional Loss SNV dbSNP153 33..33 33 - - - 4441 RMVar_ID_4441 Human_SNP_ID_455276641 A-to-I Human chr11 - 8669542 8669542 8669542 GCCTCCTGGGTTCAAGTGATTCTCCTGCGTCAACCTCCCAAATACCTGGGACTACAGCATGTGCC GCCTCCTGGGTTCAAGTGATTCTCCTGCGTCACCCTCCCAAATACCTGGGACTACAGCATGTGCC T G TRIM66 Ensembl:ENSG00000166436 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904766267 Functional Loss SNV dbSNP153 33..33 33 - - - 4442 RMVar_ID_4442 Human_SNP_ID_455280661 A-to-I Human chr11 + 8683172 8683172 8683172 TGGCGGGCATCGCCCCCTGCCCCTAATTCCTTAGGCCTTACCACCAAGCTTTTTCCACACAGCCA TGGCGGGCATCGCCCCCTGCCCCTAATTCCTTGGGCCTTACCACCAAGCTTTTTCCACACAGCCA A G RPL27A Ensembl:ENSG00000166441 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs763599632 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22537298 Human_Splice_Rec_1207421,Human_Splice_Rec_1207425,Human_Splice_Rec_1207431,Human_Splice_Rec_1207439,Human_Splice_Rec_1207447,Human_Splice_Rec_1207455,Human_Splice_Rec_1207461,Human_Splice_Rec_1207467,Human_Splice_Rec_1207473 4443 RMVar_ID_4443 Human_SNP_ID_455281821 A-to-I Human chr11 + 8686360 8686360 8686360 TTAAGCGATTCTCCTGCCTCAGCTTCCTGACTAACTGGGATTACAGGCGCCCACCACCATGCCCA TTAAGCGATTCTCCTGCCTCAGCTTCCTGACTGACTGGGATTACAGGCGCCCACCACCATGCCCA A G RPL27A Ensembl:ENSG00000166441 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1421652118 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_405558,Human_RBP_ID_17802777,Human_RBP_ID_26407711 Human_miRNA_ID_2873382 RMVar_hsa_circ_118057,RMVar_hsa_circ_147949 4444 RMVar_ID_4444 Human_SNP_ID_455281832 A-to-I Human chr11 + 8686396 8686396 8686396 GGGATTACAGGCGCCCACCACCATGCCCAGCTAATTTTTGTATTTTCAGTAGAGATGGGGTTTCA GGGATTACAGGCGCCCACCACCATGCCCAGCTGATTTTTGTATTTTCAGTAGAGATGGGGTTTCA A G RPL27A Ensembl:ENSG00000166441 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs549974868 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118057,RMVar_hsa_circ_147949 4445 RMVar_ID_4445 Human_SNP_ID_455282061 A-to-I Human chr11 + 8687235 8687235 8687235 CAGCCTGACCAACCTGGAGAAACCTTGTCTCTACTAAATACACAAAATTAGCCAGGCGTGGTGGC CAGCCTGACCAACCTGGAGAAACCTTGTCTCTGCTAAATACACAAAATTAGCCAGGCGTGGTGGC A G RPL27A Ensembl:ENSG00000166441 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs991687462 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118057,RMVar_hsa_circ_147949 4446 RMVar_ID_4446 Human_SNP_ID_455282081 A-to-I Human chr11 + 8687284 8687284 8687284 AGCCAGGCGTGGTGGCACATGCCTGTAATCCCAGCTACTTTGGAGGCTGAGCCAGGAGAATCTCC AGCCAGGCGTGGTGGCACATGCCTGTAATCCCTGCTACTTTGGAGGCTGAGCCAGGAGAATCTCC A T RPL27A Ensembl:ENSG00000166441 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1269729556 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22369689 RMVar_hsa_circ_118057,RMVar_hsa_circ_147949 4447 RMVar_ID_4447 Human_SNP_ID_455282095 A-to-I Human chr11 + 8687320 8687320 8687320 ACTTTGGAGGCTGAGCCAGGAGAATCTCCAGGAGGCGGAGGTTGCTGTGAGCCGAGATCGTGCCA ACTTTGGAGGCTGAGCCAGGAGAATCTCCAGGCGGCGGAGGTTGCTGTGAGCCGAGATCGTGCCA A C RPL27A Ensembl:ENSG00000166441 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs916351502 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22369689 RMVar_hsa_circ_118057,RMVar_hsa_circ_147949 4448 RMVar_ID_4448 Human_SNP_ID_455282284 A-to-I Human chr11 + 8687698 8687698 8687698 TCGCCCAGGCTGGAGTGCAGTGGTGCGATCTCAGATCACTGCAAGCTCCGCCTCCTAGGTTCAGA TCGCCCAGGCTGGAGTGCAGTGGTGCGATCTCGGATCACTGCAAGCTCCGCCTCCTAGGTTCAGA A G RPL27A Ensembl:ENSG00000166441 Protein coding 3'UTR GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs893106090 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6102732,Human_RBP_ID_11741104 RMVar_hsa_circ_118057,RMVar_hsa_circ_147949 4449 RMVar_ID_4449 Human_SNP_ID_455340767 A-to-I Human chr11 + 8919662 8919662 8919662 TTTTGTTTGTTTGGTTGGTTTTTTTTTGAGACAGTCTCACTCTGTTGCCCAGGCTGGAGTGCAGT TTTTGTTTGTTTGGTTGGTTTTTTTTTGAGACGGTCTCACTCTGTTGCCCAGGCTGGAGTGCAGT A G AKIP1 Ensembl:ENSG00000166452 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1354840429 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6103401 4450 RMVar_ID_4450 Human_SNP_ID_455353549 A-to-I Human chr11 + 8968599 8968599 8968599 CAGGAGGCTGAGGCATAAGAATCCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCTGAGATTGCA CAGGAGGCTGAGGCATAAGAATCCTTGAACCCGGGAGGCGGAGGTTGCAGTGAGCTGAGATTGCA A G TMEM9B-AS1 Ensembl:ENSG00000254860 lincRNA exon GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1028182388 Functional Loss SNV dbSNP153 33..33 33 - - - 4451 RMVar_ID_4451 Human_SNP_ID_455354544 A-to-I Human chr11 + 8972890 8972889 8972891 TTGGTGGTTCATGCCTGTAGTCCCAGCTACTCAAGAGACTGAGGTGGAGAATCACTTGAGCCCAG TTGGTGGTTCATGCCTGTAGTCCCAGCTACTC__GAGACTGAGGTGGAGAATCACTTGAGCCCAG CAA C TMEM9B-AS1 Ensembl:ENSG00000254860 lincRNA intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs942464103 Functional Loss DEL dbSNP153 33..34 33 - - - 4452 RMVar_ID_4452 Human_SNP_ID_455354959 A-to-I Human chr11 + 8974754 8974754 8974754 CAGAACAAGCAGGATGAAAATCACTTATCACTATAGCACCCACCCTTAAGCACAAGGTTATCCAA CAGAACAAGCAGGATGAAAATCACTTATCACTGTAGCACCCACCCTTAAGCACAAGGTTATCCAA A G TMEM9B-AS1 Ensembl:ENSG00000254860 lincRNA intron GSE123020:GSM3490829,GSM3490830,GSM3490831 esophageal squamous carcinoma cells,EC109 cell line - 32596459 RNA-Seq:(High) rs573708451 Functional Loss SNV dbSNP153 33..33 33 - - - 4453 RMVar_ID_4453 Human_SNP_ID_455355254 A-to-I Human chr11 + 8976032 8976032 8976032 TGGGGTGCAGTGGTGTGATCATAGCTCACTGCAGCCTCTGAGCTCCTGGGCTCAAGGGATCCCCC TGGGGTGCAGTGGTGTGATCATAGCTCACTGCTGCCTCTGAGCTCCTGGGCTCAAGGGATCCCCC A T TMEM9B-AS1 Ensembl:ENSG00000254860 lincRNA intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1324254341 Functional Loss SNV dbSNP153 33..33 33 - - - 4454 RMVar_ID_4454 Human_SNP_ID_455355455 A-to-I Human chr11 + 8976744 8976743 8976745 GGTAACAATATATATATATATTTTTTTGAGACAGAGTCTCGCTCTGTTGTCCAGGCTGGAGTGCA GGTAACAATATATATATATATTTTTTTGAGAC__AGTCTCGCTCTGTTGTCCAGGCTGGAGTGCA CAG C TMEM9B-AS1 Ensembl:ENSG00000254860 lincRNA intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1491512463 Functional Loss DEL dbSNP153 33..34 33 - - - 4455 RMVar_ID_4455 Human_SNP_ID_455355476 A-to-I Human chr11 + 8976800 8976800 8976800 TGGAGTGCAGTGGCGTGATCGCGGCTCACTGCAAGCTCCACCTCCCGAGTTCATGCCATTCTCCT TGGAGTGCAGTGGCGTGATCGCGGCTCACTGCTAGCTCCACCTCCCGAGTTCATGCCATTCTCCT A T TMEM9B-AS1 Ensembl:ENSG00000254860 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1566131051 Functional Loss SNV dbSNP153 33..33 33 - - - 4456 RMVar_ID_4456 Human_SNP_ID_455355493 A-to-I Human chr11 + 8976860 8976860 8976860 CTCCTGCATCAGCCTCCTGAGTAGCTGGGACTACAGGTGCCCACCACCACTCCCAGCTAATTTTT CTCCTGCATCAGCCTCCTGAGTAGCTGGGACTGCAGGTGCCCACCACCACTCCCAGCTAATTTTT A G TMEM9B-AS1 Ensembl:ENSG00000254860 lincRNA intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs971776826 Functional Loss SNV dbSNP153 33..33 33 - - - 4457 RMVar_ID_4457 Human_SNP_ID_455395674 A-to-I Human chr11 - 9142080 9142080 9142080 ACAGAAAAAGCACAAACCTATTATGAGACATTAGAGAAGAATGAAGTAGTCCCTGAGGAAAACTG ACAGAAAAAGCACAAACCTATTATGAGACATTGGAGAAGAATGAAGTAGTCCCTGAGGAAAACTG T C DENND5A Ensembl:ENSG00000184014 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1355112789 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_867153,Human_RBP_ID_1783637,Human_RBP_ID_11744853 Human_Splice_Rec_1208610,Human_Splice_Rec_1208618,Human_Splice_Rec_1208662,Human_Splice_Rec_1208666,Human_Splice_Rec_1208694,Human_Splice_Rec_1208700,Human_Splice_Rec_1208710,Human_Splice_Rec_1208724 Human_miRNA_ID_3117662 RMVar_hsa_circ_12862,RMVar_hsa_circ_78783,RMVar_hsa_circ_265448,RMVar_hsa_circ_147994 4458 RMVar_ID_4458 Human_SNP_ID_455411627 A-to-I Human chr11 - 9204117 9204117 9204117 TACCACATGCACAATGCTGAGTATGATGTCCTACATGCTCCCCCTGCTGATGACAGAGACCAGAG TACCACATGCACAATGCTGAGTATGATGTCCTGCATGCTCCCCCTGCTGATGACAGAGACCAGAG T C DENND5A Ensembl:ENSG00000184014 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1366980360 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_406062,Human_RBP_ID_1783691,Human_RBP_ID_18614418,Human_RBP_ID_23526674 Human_miRNA_ID_2221833,Human_miRNA_ID_2484889,Human_miRNA_ID_3073265 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 4459 RMVar_ID_4459 Human_SNP_ID_455420791 A-to-I Human chr11 - 9239121 9239121 9239121 TTAGAAATTGTAGAAGGATGTAGGCCGGGCGCAGTGGCTCACACCTGTAATCCCAGCATTTTGGA TTAGAAATTGTAGAAGGATGTAGGCCGGGCGCGGTGGCTCACACCTGTAATCCCAGCATTTTGGA T C DENND5A Ensembl:ENSG00000184014 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1447310026 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11746751 4460 RMVar_ID_4460 Human_SNP_ID_455422792 A-to-I Human chr11 - 9245909 9245909 9245909 AAGAGATAGGTTGGGCATGGTGGCTCACGCCTATAATCCCAGCACTTTGTGAGGCTGAGGCAGGC AAGAGATAGGTTGGGCATGGTGGCTCACGCCTGTAATCCCAGCACTTTGTGAGGCTGAGGCAGGC T C DENND5A Ensembl:ENSG00000184014 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934631506 Functional Loss SNV dbSNP153 33..33 33 - - - 4461 RMVar_ID_4461 Human_SNP_ID_455435352 A-to-I Human chr11 - 9289135 9289135 9289135 AATTGGTGTGGTGACACACGTCCGTGATCCCAACTACTTGCAAGGCTGAAGTGGGAGAATTGCTT AATTGGTGTGGTGACACACGTCCGTGATCCCAGCTACTTGCAAGGCTGAAGTGGGAGAATTGCTT T C TMEM41B Ensembl:ENSG00000166471 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1295302820 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 4462 RMVar_ID_4462 Human_SNP_ID_455435616 A-to-I Human chr11 - 9290136 9290136 9290136 GACTTTGTGATCCGCCTGCCTCAGACTCCCTAAGTGCTGGGATTACAGGCATGAGCCACCCCACC GACTTTGTGATCCGCCTGCCTCAGACTCCCTACGTGCTGGGATTACAGGCATGAGCCACCCCACC T G TMEM41B Ensembl:ENSG00000166471 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1241432795 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 4463 RMVar_ID_4463 Human_SNP_ID_455435867 A-to-I Human chr11 - 9290988 9290988 9290988 TCCCAGCCTCCTGAGTACCTGGCATTACAGGCATGAGCCACTGTGACTGGCCAATTTTTGTATTT TCCCAGCCTCCTGAGTACCTGGCATTACAGGCCTGAGCCACTGTGACTGGCCAATTTTTGTATTT T G TMEM41B Ensembl:ENSG00000166471 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs568106814 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 4464 RMVar_ID_4464 Human_SNP_ID_455435891 A-to-I Human chr11 - 9291056 9291056 9291056 GCCAGAGGTCAGTGGCATGATCTCGGCTCACTACAACGTCTGCCCTCTGGGTTCAAGAGATTCTC GCCAGAGGTCAGTGGCATGATCTCGGCTCACTGCAACGTCTGCCCTCTGGGTTCAAGAGATTCTC T C TMEM41B Ensembl:ENSG00000166471 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs995389639 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_808784 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 4465 RMVar_ID_4465 Human_SNP_ID_455435956 A-to-I Human chr11 - 9291258 9291258 9291258 CCTGCTTCAGCTTGCCAAGTAGCTGAGATTACAGGCACCTGCCACTGCGCCCGGCTAATTTTTTG CCTGCTTCAGCTTGCCAAGTAGCTGAGATTACGGGCACCTGCCACTGCGCCCGGCTAATTTTTTG T C TMEM41B Ensembl:ENSG00000166471 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1333794938 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 4466 RMVar_ID_4466 Human_SNP_ID_455435957 A-to-I Human chr11 - 9291260 9291260 9291260 CTCCTGCTTCAGCTTGCCAAGTAGCTGAGATTACAGGCACCTGCCACTGCGCCCGGCTAATTTTT CTCCTGCTTCAGCTTGCCAAGTAGCTGAGATTCCAGGCACCTGCCACTGCGCCCGGCTAATTTTT T G TMEM41B Ensembl:ENSG00000166471 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978549057 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 4467 RMVar_ID_4467 Human_SNP_ID_455435970 A-to-I Human chr11 - 9291295 9291295 9291295 CCACTGCAACCTCCGCTGCCCGAGTTCAAGCAATTCTCCTGCTTCAGCTTGCCAAGTAGCTGAGA CCACTGCAACCTCCGCTGCCCGAGTTCAAGCAGTTCTCCTGCTTCAGCTTGCCAAGTAGCTGAGA T C TMEM41B Ensembl:ENSG00000166471 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1156792698 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24908643 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 4468 RMVar_ID_4468 Human_SNP_ID_455435971 A-to-I Human chr11 - 9291296 9291296 9291296 CCCACTGCAACCTCCGCTGCCCGAGTTCAAGCAATTCTCCTGCTTCAGCTTGCCAAGTAGCTGAG CCCACTGCAACCTCCGCTGCCCGAGTTCAAGCGATTCTCCTGCTTCAGCTTGCCAAGTAGCTGAG T C TMEM41B Ensembl:ENSG00000166471 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1022189155 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24908643 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 4469 RMVar_ID_4469 Human_SNP_ID_455436118 A-to-I Human chr11 - 9291672 9291672 9291672 GGAATTGGCCGGGCGTGGTGGCCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGCGGGGTGGA GGAATTGGCCGGGCGTGGTGGCCACACCTGTATTCCCAGCACTTTGGGAGGCCAAGCGGGGTGGA T A TMEM41B Ensembl:ENSG00000166471 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879554235 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226891,Human_RBP_ID_22471567 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 4470 RMVar_ID_4470 Human_SNP_ID_455436147 A-to-I Human chr11 - 9291756 9291756 9291756 TGCAGTGAGCTGAGATCACGCCACTGCCCTCCAGCCTGGACGACAGAGCGAGACTCCTACCACAA TGCAGTGAGCTGAGATCACGCCACTGCCCTCCGGCCTGGACGACAGAGCGAGACTCCTACCACAA T C TMEM41B Ensembl:ENSG00000166471 Protein coding intron GSE38233;GSE100210;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,temporal_cortex - 24183664,29129909,30559470 RNA-Seq:(High) rs1177011565 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11748156 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 4471 RMVar_ID_4471 Human_SNP_ID_455436198 A-to-I Human chr11 - 9291981 9291981 9291981 GAAAAGGAGGCCAGGCACGGTGGCTAACACCTATAATTCCAGTACTTTGGGAGGCCGAGGCAGGT GAAAAGGAGGCCAGGCACGGTGGCTAACACCTGTAATTCCAGTACTTTGGGAGGCCGAGGCAGGT T C TMEM41B Ensembl:ENSG00000166471 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965582817 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24908661 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 4472 RMVar_ID_4472 Human_SNP_ID_455436369 A-to-I Human chr11 - 9292696 9292696 9292696 TTGGGAGTTCAAGACCAGCCTGACCAACATGAAGAAATCCCGTCTCTTCATGTATTTTTTTGTAG TTGGGAGTTCAAGACCAGCCTGACCAACATGAGGAAATCCCGTCTCTTCATGTATTTTTTTGTAG T C TMEM41B Ensembl:ENSG00000166471 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1401291381 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 4473 RMVar_ID_4473 Human_SNP_ID_455436391 A-to-I Human chr11 - 9292774 9292774 9292774 ATTATCAGGGCCGGGTGTGGTGGCTCACACCTATAATCCCAGCACTTTGGGAGACCGAGGCAGGC ATTATCAGGGCCGGGTGTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGACCGAGGCAGGC T C TMEM41B Ensembl:ENSG00000166471 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs908050577 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 4474 RMVar_ID_4474 Human_SNP_ID_455436502 A-to-I Human chr11 - 9293210 9293210 9293210 TAGTCCTAGCTACTTGGGAGGCTGAGGTGGGAAGATCACCTGAGCCCAGGGAAGTTGAGGCTACA TAGTCCTAGCTACTTGGGAGGCTGAGGTGGGAGGATCACCTGAGCCCAGGGAAGTTGAGGCTACA T C TMEM41B Ensembl:ENSG00000166471 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1045641015 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17559842 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 4475 RMVar_ID_4475 Human_SNP_ID_455436503 A-to-I Human chr11 - 9293210 9293210 9293210 TAGTCCTAGCTACTTGGGAGGCTGAGGTGGGAAGATCACCTGAGCCCAGGGAAGTTGAGGCTACA TAGTCCTAGCTACTTGGGAGGCTGAGGTGGGACGATCACCTGAGCCCAGGGAAGTTGAGGCTACA T G TMEM41B Ensembl:ENSG00000166471 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1045641015 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17559842 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 4476 RMVar_ID_4476 Human_SNP_ID_455436716 A-to-I Human chr11 - 9294007 9294007 9294007 TTGGGATTTATTTGTAGATGCCAGGTTTTGCTATGTTGTCTGGGCTGGTGTTGAACTCCTGAGCT TTGGGATTTATTTGTAGATGCCAGGTTTTGCTTTGTTGTCTGGGCTGGTGTTGAACTCCTGAGCT T A TMEM41B Ensembl:ENSG00000166471 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs771290393 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6105477,Human_RBP_ID_11748197,Human_RBP_ID_17560261 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 4477 RMVar_ID_4477 Human_SNP_ID_455436717 A-to-I Human chr11 - 9294007 9294007 9294007 TTGGGATTTATTTGTAGATGCCAGGTTTTGCTATGTTGTCTGGGCTGGTGTTGAACTCCTGAGCT TTGGGATTTATTTGTAGATGCCAGGTTTTGCTGTGTTGTCTGGGCTGGTGTTGAACTCCTGAGCT T C TMEM41B Ensembl:ENSG00000166471 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs771290393 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6105477,Human_RBP_ID_11748197,Human_RBP_ID_17560261 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 4478 RMVar_ID_4478 Human_SNP_ID_455436871 A-to-I Human chr11 - 9294449 9294449 9294449 AGTTTTGCTCTTGTTACACAGGCTGGAGGCACAATCTCTGGTCACTGCAACCTCCACCTCCTAGG AGTTTTGCTCTTGTTACACAGGCTGGAGGCACGATCTCTGGTCACTGCAACCTCCACCTCCTAGG T C TMEM41B Ensembl:ENSG00000166471 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs916036091 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6105479 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 4479 RMVar_ID_4479 Human_SNP_ID_455437167 A-to-I Human chr11 - 9295650 9295650 9295650 CACGCCTGTGATCCCAGCTTCTCAGAAGGCTGAGGCAGGAGAATCGTTTGTACCTGGGAGGCAGA CACGCCTGTGATCCCAGCTTCTCAGAAGGCTGTGGCAGGAGAATCGTTTGTACCTGGGAGGCAGA T A TMEM41B Ensembl:ENSG00000166471 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1021956191 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_284958,RMVar_hsa_circ_148039,RMVar_hsa_circ_148042,RMVar_hsa_circ_270143,RMVar_hsa_circ_323450,RMVar_hsa_circ_148044,RMVar_hsa_circ_62939 4480 RMVar_ID_4480 Human_SNP_ID_455437262 A-to-I Human chr11 - 9296052 9296052 9296052 AGGAATTTGAGACCAGCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAG AGGAATTTGAGACCAGCCTGGCCAACATGGTGGAACCCCGTCTCTACTAAAAATACAAAAATTAG T C TMEM41B Ensembl:ENSG00000166471 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs962872992 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_284958,RMVar_hsa_circ_148039,RMVar_hsa_circ_148042,RMVar_hsa_circ_270143,RMVar_hsa_circ_323450,RMVar_hsa_circ_148044,RMVar_hsa_circ_62939 4481 RMVar_ID_4481 Human_SNP_ID_455437263 A-to-I Human chr11 - 9296058 9296058 9296058 AAGGTCAGGAATTTGAGACCAGCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAA AAGGTCAGGAATTTGAGACCAGCCTGGCCAACGTGGTGAAACCCCGTCTCTACTAAAAATACAAA T C TMEM41B Ensembl:ENSG00000166471 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs532375328 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_284958,RMVar_hsa_circ_148039,RMVar_hsa_circ_148042,RMVar_hsa_circ_270143,RMVar_hsa_circ_323450,RMVar_hsa_circ_148044,RMVar_hsa_circ_62939 4482 RMVar_ID_4482 Human_SNP_ID_455437654 A-to-I Human chr11 - 9297267 9297267 9297267 CAGACTGGCTAACGTGGAGAAACCCCATCTCTACTAAAAATAAAAAAATTAGCTGGGCGTGGTGG CAGACTGGCTAACGTGGAGAAACCCCATCTCTGCTAAAAATAAAAAAATTAGCTGGGCGTGGTGG T C TMEM41B Ensembl:ENSG00000166471 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1214293272 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_284958,RMVar_hsa_circ_148039,RMVar_hsa_circ_148042,RMVar_hsa_circ_270143,RMVar_hsa_circ_323450,RMVar_hsa_circ_148044,RMVar_hsa_circ_62939 4483 RMVar_ID_4483 Human_SNP_ID_455437749 A-to-I Human chr11 - 9297609 9297609 9297609 TTGGCTTACTGCAGCCCCCACCTCCCAGTTCAAGCGATTCTCCTGCCTCAGGCTCCCAAGTAGTT TTGGCTTACTGCAGCCCCCACCTCCCAGTTCAGGCGATTCTCCTGCCTCAGGCTCCCAAGTAGTT T C TMEM41B Ensembl:ENSG00000166471 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs974231390 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_284958,RMVar_hsa_circ_148039,RMVar_hsa_circ_148042,RMVar_hsa_circ_270143,RMVar_hsa_circ_323450,RMVar_hsa_circ_148044,RMVar_hsa_circ_62939 4484 RMVar_ID_4484 Human_SNP_ID_455440499 A-to-I Human chr11 - 9306634 9306634 9306634 TCGCCCAGGCTAGAGTGCGGTGGCGCCATCTCAGCTCACTGCAAGCTCCGCCTCCCGGGTTAATG TCGCCCAGGCTAGAGTGCGGTGGCGCCATCTCCGCTCACTGCAAGCTCCGCCTCCCGGGTTAATG T G TMEM41B Ensembl:ENSG00000166471 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202931358 Functional Loss SNV dbSNP153 33..33 33 - - - 4485 RMVar_ID_4485 Human_SNP_ID_455440745 A-to-I Human chr11 - 9307580 9307580 9307580 AAATTAGCCGGACGTGGTGGCCCACGCCTGTAATCCCAGCTACTTGGGAGGCTAAGGCAGGAGAA AAATTAGCCGGACGTGGTGGCCCACGCCTGTAGTCCCAGCTACTTGGGAGGCTAAGGCAGGAGAA T C TMEM41B Ensembl:ENSG00000166471 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1354628563 Functional Loss SNV dbSNP153 33..33 33 - - - 4486 RMVar_ID_4486 Human_SNP_ID_455440858 A-to-I Human chr11 - 9307943 9307943 9307943 TCACGAGGTCAGGAGATCCAGACCACGGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTAGC TCACGAGGTCAGGAGATCCAGACCACGGTGAAGCCCCGTCTCTACTAAAAATACAAAAAATTAGC T C TMEM41B Ensembl:ENSG00000166471 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1045309364 Functional Loss SNV dbSNP153 33..33 33 - - - 4487 RMVar_ID_4487 Human_SNP_ID_455464718 A-to-I Human chr11 + 9388814 9388814 9388814 CTAGAACTCTTGGCCTCAAGCAGCGTCCTCCCATCTGAGCCTCCCAGGTGGCTGGGACTGCAGAC CTAGAACTCTTGGCCTCAAGCAGCGTCCTCCCGTCTGAGCCTCCCAGGTGGCTGGGACTGCAGAC A G IPO7 Ensembl:ENSG00000205339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10840229 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_148045,RMVar_hsa_circ_76887,RMVar_hsa_circ_120890,RMVar_hsa_circ_148046 4488 RMVar_ID_4488 Human_SNP_ID_455464794 A-to-I Human chr11 + 9389102 9389102 9389102 TTGTGGCAGGTTCTCACTCGGTTGCCCAGGCTAGAGTGCGGTGGCATGATCTTGGCTCACTGTAG TTGTGGCAGGTTCTCACTCGGTTGCCCAGGCTGGAGTGCGGTGGCATGATCTTGGCTCACTGTAG A G IPO7 Ensembl:ENSG00000205339 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1474522348 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11751227 RMVar_hsa_circ_148045,RMVar_hsa_circ_76887,RMVar_hsa_circ_120890,RMVar_hsa_circ_148046 4489 RMVar_ID_4489 Human_SNP_ID_455465697 A-to-I Human chr11 + 9392307 9392307 9392307 TCGGGCAATTCTCCTGCCTCAGCCTCTTGAGTAGCTGGGATTACAGGTATGCATTACCACGTCCG TCGGGCAATTCTCCTGCCTCAGCCTCTTGAGTCGCTGGGATTACAGGTATGCATTACCACGTCCG A C IPO7 Ensembl:ENSG00000205339 Protein coding stop codon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1375372964 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1208863 RMVar_hsa_circ_148045,RMVar_hsa_circ_76887,RMVar_hsa_circ_120890,RMVar_hsa_circ_148046 4490 RMVar_ID_4490 Human_SNP_ID_455465730 A-to-I Human chr11 + 9392377 9392377 9392377 TTTTGTATTTTTAGTAGAGACGGGGTTTCTCCATGTTGGTAGGCTGGTCTCGAACTCCCGAGATC TTTTGTATTTTTAGTAGAGACGGGGTTTCTCCCTGTTGGTAGGCTGGTCTCGAACTCCCGAGATC A C IPO7 Ensembl:ENSG00000205339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs902492332 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_148045,RMVar_hsa_circ_76887,RMVar_hsa_circ_120890,RMVar_hsa_circ_148046 4491 RMVar_ID_4491 Human_SNP_ID_455465863 A-to-I Human chr11 + 9392898 9392892 9392899 TTGAACCTGGGAGGCAGTGGCTGAAGTGAGCCAAGATTGCTCCACTGCACTCTAGCCTGGGCGAC TTGAACCTGGGAGGCAGTGGCTGAAGT_______GATTGCTCCACTGCACTCTAGCCTGGGCGAC TGAGCCAA T IPO7 Ensembl:ENSG00000205339 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1399895832 Functional Loss DEL dbSNP153 28..34 33 - - - Human_RBP_ID_22709815 RMVar_hsa_circ_148045,RMVar_hsa_circ_76887,RMVar_hsa_circ_120890,RMVar_hsa_circ_148046 4492 RMVar_ID_4492 Human_SNP_ID_455466445 A-to-I Human chr11 + 9395323 9395323 9395323 TAGAGTGCAGTGGTACGATCTCGGCTCACTGCAGCCTCCACCTCCCAGGTTCAAGCCATTCTCCA TAGAGTGCAGTGGTACGATCTCGGCTCACTGCGGCCTCCACCTCCCAGGTTCAAGCCATTCTCCA A G IPO7 Ensembl:ENSG00000205339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs955543455 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_148045,RMVar_hsa_circ_76887,RMVar_hsa_circ_120890,RMVar_hsa_circ_148046 4493 RMVar_ID_4493 Human_SNP_ID_455466460 A-to-I Human chr11 + 9395361 9395361 9395361 CACCTCCCAGGTTCAAGCCATTCTCCAGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCGCCCC CACCTCCCAGGTTCAAGCCATTCTCCAGCCTCGGCCTCCTGAGTAGCTGGGATTACAGGCGCCCC A G IPO7 Ensembl:ENSG00000205339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1168233180 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_148045,RMVar_hsa_circ_76887,RMVar_hsa_circ_120890,RMVar_hsa_circ_148046 4494 RMVar_ID_4494 Human_SNP_ID_455466482 A-to-I Human chr11 + 9395424 9395424 9395424 CCCCACTGTGCCCGGTTAATTGTATGTTTACCAGAGATGGGGTTTCACCATGTTGGCCAGGCTGG CCCCACTGTGCCCGGTTAATTGTATGTTTACCGGAGATGGGGTTTCACCATGTTGGCCAGGCTGG A G IPO7 Ensembl:ENSG00000205339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs984094063 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_148045,RMVar_hsa_circ_76887,RMVar_hsa_circ_120890,RMVar_hsa_circ_148046 4495 RMVar_ID_4495 Human_SNP_ID_455468837 A-to-I Human chr11 + 9403941 9403941 9403941 TGGAGTGCAGTGGTGCGAACTCGGCTCTCTGCAACCTCTGCCTCCCAGGTTCAAGCGATTCTTCT TGGAGTGCAGTGGTGCGAACTCGGCTCTCTGCGACCTCTGCCTCCCAGGTTCAAGCGATTCTTCT A G IPO7 Ensembl:ENSG00000205339 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1304926597 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7109,RMVar_hsa_circ_148045,RMVar_hsa_circ_76887,RMVar_hsa_circ_120890,RMVar_hsa_circ_148046,RMVar_hsa_circ_282180,RMVar_hsa_circ_304945,RMVar_hsa_circ_338019,RMVar_hsa_circ_345346,RMVar_hsa_circ_293543,RMVar_hsa_circ_29699 4496 RMVar_ID_4496 Human_SNP_ID_455476908 A-to-I Human chr11 + 9431916 9431916 9431916 AGAATCACTTGAACCCGAGAGGCAGACGCTGCAGTGAGCATAGATCGCGCCACTGCACTCCAGCC AGAATCACTTGAACCCGAGAGGCAGACGCTGCGGTGAGCATAGATCGCGCCACTGCACTCCAGCC A G IPO7 Ensembl:ENSG00000205339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs531375027 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2869,RMVar_hsa_circ_39262,RMVar_hsa_circ_120890,RMVar_hsa_circ_148046,RMVar_hsa_circ_125379,RMVar_hsa_circ_358273,RMVar_hsa_circ_117165,RMVar_hsa_circ_148048,RMVar_hsa_circ_148049,RMVar_hsa_circ_148047,RMVar_hsa_circ_109421,RMVar_hsa_circ_105672,RMVar_hsa_circ_148058,RMVar_hsa_circ_148059,RMVar_hsa_circ_49314,RMVar_hsa_circ_148065,RMVar_hsa_circ_87638,RMVar_hsa_circ_320145,RMVar_hsa_circ_376169,RMVar_hsa_circ_355156,RMVar_hsa_circ_313579,RMVar_hsa_circ_127808,RMVar_hsa_circ_95818,RMVar_hsa_circ_148061,RMVar_hsa_circ_148063,RMVar_hsa_circ_148064,RMVar_hsa_circ_148062,RMVar_hsa_circ_123213,RMVar_hsa_circ_148060,RMVar_hsa_circ_36610,RMVar_hsa_circ_71750,RMVar_hsa_circ_148073,RMVar_hsa_circ_111363,RMVar_hsa_circ_148075,RMVar_hsa_circ_47193,RMVar_hsa_circ_148074,RMVar_hsa_circ_318697,RMVar_hsa_circ_323205,RMVar_hsa_circ_22660,RMVar_hsa_circ_148083,RMVar_hsa_circ_148086,RMVar_hsa_circ_78637,RMVar_hsa_circ_300253,RMVar_hsa_circ_312418,RMVar_hsa_circ_353630,RMVar_hsa_circ_303426,RMVar_hsa_circ_31735,RMVar_hsa_circ_110535,RMVar_hsa_circ_148087,RMVar_hsa_circ_371003,RMVar_hsa_circ_105631,RMVar_hsa_circ_148091,RMVar_hsa_circ_148092,RMVar_hsa_circ_148090 4497 RMVar_ID_4497 Human_SNP_ID_455477071 A-to-I Human chr11 + 9432435 9432435 9432435 TGTTGGCCGGCAGGTCTGGAACTCCTGACCTCAAGTGATCCGCCTCCCTTGACCTCCCAAAGTGC TGTTGGCCGGCAGGTCTGGAACTCCTGACCTCCAGTGATCCGCCTCCCTTGACCTCCCAAAGTGC A C IPO7 Ensembl:ENSG00000205339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs192283557 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2869,RMVar_hsa_circ_39262,RMVar_hsa_circ_120890,RMVar_hsa_circ_148046,RMVar_hsa_circ_125379,RMVar_hsa_circ_358273,RMVar_hsa_circ_117165,RMVar_hsa_circ_148048,RMVar_hsa_circ_148049,RMVar_hsa_circ_148047,RMVar_hsa_circ_109421,RMVar_hsa_circ_105672,RMVar_hsa_circ_148058,RMVar_hsa_circ_148059,RMVar_hsa_circ_49314,RMVar_hsa_circ_148065,RMVar_hsa_circ_87638,RMVar_hsa_circ_320145,RMVar_hsa_circ_376169,RMVar_hsa_circ_355156,RMVar_hsa_circ_313579,RMVar_hsa_circ_127808,RMVar_hsa_circ_95818,RMVar_hsa_circ_148061,RMVar_hsa_circ_148063,RMVar_hsa_circ_148064,RMVar_hsa_circ_148062,RMVar_hsa_circ_123213,RMVar_hsa_circ_148060,RMVar_hsa_circ_36610,RMVar_hsa_circ_71750,RMVar_hsa_circ_148073,RMVar_hsa_circ_111363,RMVar_hsa_circ_148075,RMVar_hsa_circ_47193,RMVar_hsa_circ_148074,RMVar_hsa_circ_318697,RMVar_hsa_circ_323205,RMVar_hsa_circ_22660,RMVar_hsa_circ_148083,RMVar_hsa_circ_148086,RMVar_hsa_circ_78637,RMVar_hsa_circ_300253,RMVar_hsa_circ_312418,RMVar_hsa_circ_353630,RMVar_hsa_circ_303426,RMVar_hsa_circ_31735,RMVar_hsa_circ_110535,RMVar_hsa_circ_148087,RMVar_hsa_circ_371003,RMVar_hsa_circ_105631,RMVar_hsa_circ_148091,RMVar_hsa_circ_148092,RMVar_hsa_circ_148090 4498 RMVar_ID_4498 Human_SNP_ID_455477757 A-to-I Human chr11 + 9434670 9434670 9434670 TAAAAATTAATCAGGCGAGGTGGCGTGTGCCTATAGTCCCAGCTACCTGGGTGGCTGAGGTGGGA TAAAAATTAATCAGGCGAGGTGGCGTGTGCCTGTAGTCCCAGCTACCTGGGTGGCTGAGGTGGGA A G IPO7 Ensembl:ENSG00000205339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1480725334 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39262,RMVar_hsa_circ_120890,RMVar_hsa_circ_148046,RMVar_hsa_circ_358273,RMVar_hsa_circ_117165,RMVar_hsa_circ_148048,RMVar_hsa_circ_148047,RMVar_hsa_circ_109421,RMVar_hsa_circ_105672,RMVar_hsa_circ_148058,RMVar_hsa_circ_148059,RMVar_hsa_circ_49314,RMVar_hsa_circ_87638,RMVar_hsa_circ_376169,RMVar_hsa_circ_355156,RMVar_hsa_circ_313579,RMVar_hsa_circ_127808,RMVar_hsa_circ_95818,RMVar_hsa_circ_148061,RMVar_hsa_circ_148063,RMVar_hsa_circ_148064,RMVar_hsa_circ_148062,RMVar_hsa_circ_123213,RMVar_hsa_circ_148060,RMVar_hsa_circ_36610,RMVar_hsa_circ_71750,RMVar_hsa_circ_148073,RMVar_hsa_circ_111363,RMVar_hsa_circ_148075,RMVar_hsa_circ_47193,RMVar_hsa_circ_148074,RMVar_hsa_circ_318697,RMVar_hsa_circ_323205,RMVar_hsa_circ_148083,RMVar_hsa_circ_148086,RMVar_hsa_circ_78637,RMVar_hsa_circ_300253,RMVar_hsa_circ_312418,RMVar_hsa_circ_353630,RMVar_hsa_circ_31735,RMVar_hsa_circ_371003,RMVar_hsa_circ_316929,RMVar_hsa_circ_148092,RMVar_hsa_circ_148093,RMVar_hsa_circ_102630,RMVar_hsa_circ_367346 4499 RMVar_ID_4499 Human_SNP_ID_455477758 A-to-I Human chr11 + 9434672 9434672 9434672 AAAATTAATCAGGCGAGGTGGCGTGTGCCTATAGTCCCAGCTACCTGGGTGGCTGAGGTGGGAGG AAAATTAATCAGGCGAGGTGGCGTGTGCCTATGGTCCCAGCTACCTGGGTGGCTGAGGTGGGAGG A G IPO7 Ensembl:ENSG00000205339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs910725704 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39262,RMVar_hsa_circ_120890,RMVar_hsa_circ_148046,RMVar_hsa_circ_358273,RMVar_hsa_circ_117165,RMVar_hsa_circ_148048,RMVar_hsa_circ_148047,RMVar_hsa_circ_109421,RMVar_hsa_circ_105672,RMVar_hsa_circ_148058,RMVar_hsa_circ_148059,RMVar_hsa_circ_49314,RMVar_hsa_circ_87638,RMVar_hsa_circ_376169,RMVar_hsa_circ_355156,RMVar_hsa_circ_313579,RMVar_hsa_circ_127808,RMVar_hsa_circ_95818,RMVar_hsa_circ_148061,RMVar_hsa_circ_148063,RMVar_hsa_circ_148064,RMVar_hsa_circ_148062,RMVar_hsa_circ_123213,RMVar_hsa_circ_148060,RMVar_hsa_circ_36610,RMVar_hsa_circ_71750,RMVar_hsa_circ_148073,RMVar_hsa_circ_111363,RMVar_hsa_circ_148075,RMVar_hsa_circ_47193,RMVar_hsa_circ_148074,RMVar_hsa_circ_318697,RMVar_hsa_circ_323205,RMVar_hsa_circ_148083,RMVar_hsa_circ_148086,RMVar_hsa_circ_78637,RMVar_hsa_circ_300253,RMVar_hsa_circ_312418,RMVar_hsa_circ_353630,RMVar_hsa_circ_31735,RMVar_hsa_circ_371003,RMVar_hsa_circ_316929,RMVar_hsa_circ_148092,RMVar_hsa_circ_148093,RMVar_hsa_circ_102630,RMVar_hsa_circ_367346 4500 RMVar_ID_4500 Human_SNP_ID_455480177 A-to-I Human chr11 + 9442687 9442687 9442687 CGCCCGCCTCGGCCTCCCAAACTGCTGAGATTACAGGCGTGAGCCACCACACCCAGCCCCAGTTT CGCCCGCCTCGGCCTCCCAAACTGCTGAGATTGCAGGCGTGAGCCACCACACCCAGCCCCAGTTT A G IPO7 Ensembl:ENSG00000205339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs994980100 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22709816,Human_RBP_ID_23155323 RMVar_hsa_circ_127808,RMVar_hsa_circ_148060,RMVar_hsa_circ_95475,RMVar_hsa_circ_148096,RMVar_hsa_circ_97908,RMVar_hsa_circ_148099,RMVar_hsa_circ_126176,RMVar_hsa_circ_148100 4501 RMVar_ID_4501 Human_SNP_ID_455480228 A-to-I Human chr11 + 9442900 9442900 9442900 AAAAAACTAGCCAGGCATGGTGGCACATGCCTATATTCCCAGCTACTCAGGAGGCTGAGGCAGGA AAAAAACTAGCCAGGCATGGTGGCACATGCCTGTATTCCCAGCTACTCAGGAGGCTGAGGCAGGA A G IPO7 Ensembl:ENSG00000205339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs930356824 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127808,RMVar_hsa_circ_148060,RMVar_hsa_circ_95475,RMVar_hsa_circ_148096,RMVar_hsa_circ_97908,RMVar_hsa_circ_148099,RMVar_hsa_circ_126176,RMVar_hsa_circ_148100 4502 RMVar_ID_4502 Human_SNP_ID_455480596 A-to-I Human chr11 + 9444167 9444167 9444167 GGACATGGTGGTGCACACCTGTAGTCCCAGCTACTTGGGAAGCAGAGGCAGGAGAATCGCTCGAA GGACATGGTGGTGCACACCTGTAGTCCCAGCTGCTTGGGAAGCAGAGGCAGGAGAATCGCTCGAA A G IPO7 Ensembl:ENSG00000205339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1036297077 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127808,RMVar_hsa_circ_148060,RMVar_hsa_circ_95475,RMVar_hsa_circ_148096,RMVar_hsa_circ_97908,RMVar_hsa_circ_148099,RMVar_hsa_circ_126176,RMVar_hsa_circ_148100 4503 RMVar_ID_4503 Human_SNP_ID_455480712 A-to-I Human chr11 + 9444543 9444543 9444543 CACCACCACACCCAACTAATTTTTGTATTTTTAGTAGAGACGAGGTTTCACTATGTTGGCCAGGC CACCACCACACCCAACTAATTTTTGTATTTTTGGTAGAGACGAGGTTTCACTATGTTGGCCAGGC A G IPO7 Ensembl:ENSG00000205339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs551695848 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127808,RMVar_hsa_circ_148060,RMVar_hsa_circ_95475,RMVar_hsa_circ_148096,RMVar_hsa_circ_97908,RMVar_hsa_circ_148099,RMVar_hsa_circ_126176,RMVar_hsa_circ_148100 4504 RMVar_ID_4504 Human_SNP_ID_455481075 A-to-I Human chr11 - 9445987 9445987 9445987 TAGCAGCAATGAAATACCACTAACCCCTTTTTACATACCGAATTCAAGTCACTATCAGAGGTGAG TAGCAGCAATGAAATACCACTAACCCCTTTTTGCATACCGAATTCAAGTCACTATCAGAGGTGAG T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs758596796 Functional Loss SNV dbSNP153 33..33 33 - - - 4505 RMVar_ID_4505 Human_SNP_ID_455486573 A-to-I Human chr11 + 9464201 9464201 9464201 TCACCCAGACTGGAGTGCAGTGGCATGATCTCAGCTCACTGCAGCCTCAACCTCCCTGGCACAAG TCACCCAGACTGGAGTGCAGTGGCATGATCTCGGCTCACTGCAGCCTCAACCTCCCTGGCACAAG A G ZNF143 Ensembl:ENSG00000166478 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs926026046 Functional Loss SNV dbSNP153 33..33 33 - - - 4506 RMVar_ID_4506 Human_SNP_ID_455486610 A-to-I Human chr11 + 9464343 9464343 9464343 CGTTTGTAGGCCAGGCGTGGTGGCTCACGCCTATAATCCCAGTACTTTGGGAGGCTGAGGCAGGT CGTTTGTAGGCCAGGCGTGGTGGCTCACGCCTGTAATCCCAGTACTTTGGGAGGCTGAGGCAGGT A G ZNF143 Ensembl:ENSG00000166478 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1236857229 Functional Loss SNV dbSNP153 33..33 33 - - - 4507 RMVar_ID_4507 Human_SNP_ID_455492313 A-to-I Human chr11 + 9482469 9482469 9482469 ATTTTTTGTATTTTTAGTACAGATGGGGTTTCACTGTGTTAGCCAGGATGGTCTCGATCTCCTGA ATTTTTTGTATTTTTAGTACAGATGGGGTTTCCCTGTGTTAGCCAGGATGGTCTCGATCTCCTGA A C ZNF143 Ensembl:ENSG00000166478 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1004132440 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34486,RMVar_hsa_circ_7369,RMVar_hsa_circ_316548,RMVar_hsa_circ_73911,RMVar_hsa_circ_109232,RMVar_hsa_circ_37825,RMVar_hsa_circ_38199,RMVar_hsa_circ_148106,RMVar_hsa_circ_265513,RMVar_hsa_circ_268350,RMVar_hsa_circ_148107,RMVar_hsa_circ_121245 4508 RMVar_ID_4508 Human_SNP_ID_455492314 A-to-I Human chr11 + 9482469 9482469 9482469 ATTTTTTGTATTTTTAGTACAGATGGGGTTTCACTGTGTTAGCCAGGATGGTCTCGATCTCCTGA ATTTTTTGTATTTTTAGTACAGATGGGGTTTCGCTGTGTTAGCCAGGATGGTCTCGATCTCCTGA A G ZNF143 Ensembl:ENSG00000166478 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1004132440 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34486,RMVar_hsa_circ_7369,RMVar_hsa_circ_316548,RMVar_hsa_circ_73911,RMVar_hsa_circ_109232,RMVar_hsa_circ_37825,RMVar_hsa_circ_38199,RMVar_hsa_circ_148106,RMVar_hsa_circ_265513,RMVar_hsa_circ_268350,RMVar_hsa_circ_148107,RMVar_hsa_circ_121245 4509 RMVar_ID_4509 Human_SNP_ID_455505189 A-to-I Human chr11 + 9526311 9526311 9526311 GGGAGGTTGAGGCTGCAGTGAGCCAAGATCGCACCACTGTACTCCAGCCTGGGCAACAGAGCGAG GGGAGGTTGAGGCTGCAGTGAGCCAAGATCGCGCCACTGTACTCCAGCCTGGGCAACAGAGCGAG A G ZNF143 Ensembl:ENSG00000166478 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1465813076 Functional Loss SNV dbSNP153 33..33 33 - - - 4510 RMVar_ID_4510 Human_SNP_ID_455519646 A-to-I Human chr11 + 9582748 9582748 9582748 ACCACCATGCCCGGCTAATTTTTTGTATTTTTAGTAGAGACGGGTTTCACCATGTTGGCTAAGCT ACCACCATGCCCGGCTAATTTTTTGTATTTTTGGTAGAGACGGGTTTCACCATGTTGGCTAAGCT A G WEE1 Ensembl:ENSG00000166483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1480788358 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24911607 RMVar_hsa_circ_94359,RMVar_hsa_circ_30272,RMVar_hsa_circ_300642,RMVar_hsa_circ_148112 4511 RMVar_ID_4511 Human_SNP_ID_455519647 A-to-I Human chr11 + 9582751 9582751 9582751 ACCATGCCCGGCTAATTTTTTGTATTTTTAGTAGAGACGGGTTTCACCATGTTGGCTAAGCTGGT ACCATGCCCGGCTAATTTTTTGTATTTTTAGTGGAGACGGGTTTCACCATGTTGGCTAAGCTGGT A G WEE1 Ensembl:ENSG00000166483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1300145601 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94359,RMVar_hsa_circ_30272,RMVar_hsa_circ_300642,RMVar_hsa_circ_148112 4512 RMVar_ID_4512 Human_SNP_ID_455519674 A-to-I Human chr11 + 9582825 9582825 9582825 TTGACCTTGTGATCTGCCCACCATGGCCTCCCAAAGTGCTGAGATTACAGGCGTAAGCCACCGTG TTGACCTTGTGATCTGCCCACCATGGCCTCCCGAAGTGCTGAGATTACAGGCGTAAGCCACCGTG A G WEE1 Ensembl:ENSG00000166483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs550565943 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94359,RMVar_hsa_circ_30272,RMVar_hsa_circ_300642,RMVar_hsa_circ_148112 4513 RMVar_ID_4513 Human_SNP_ID_455520386 A-to-I Human chr11 + 9584107 9584107 9584107 ACCTCAAGTGATCCGCCCACCTTGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCACTC ACCTCAAGTGATCCGCCCACCTTGGCCTCCCAGAGTGCTGGGATTACAGGTGTGAGCCACCACTC A G WEE1 Ensembl:ENSG00000166483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1358007298 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94359,RMVar_hsa_circ_30272,RMVar_hsa_circ_300642,RMVar_hsa_circ_148112 4514 RMVar_ID_4514 Human_SNP_ID_455520413 A-to-I Human chr11 + 9584210 9584210 9584210 CAGGCTAGAATGCAGTGGTGCAATTATAGCTCACTGCAGCTTTGAATTCCTGGGCTCAAATGAAC CAGGCTAGAATGCAGTGGTGCAATTATAGCTCGCTGCAGCTTTGAATTCCTGGGCTCAAATGAAC A G WEE1 Ensembl:ENSG00000166483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1275968078 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94359,RMVar_hsa_circ_30272,RMVar_hsa_circ_300642,RMVar_hsa_circ_148112 4515 RMVar_ID_4515 Human_SNP_ID_455520417 A-to-I Human chr11 + 9584236 9584236 9584236 TAGCTCACTGCAGCTTTGAATTCCTGGGCTCAAATGAACCTCCTGCCTCAGACTCACAAGTAGCT TAGCTCACTGCAGCTTTGAATTCCTGGGCTCAGATGAACCTCCTGCCTCAGACTCACAAGTAGCT A G WEE1 Ensembl:ENSG00000166483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1400802486 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11758369 RMVar_hsa_circ_94359,RMVar_hsa_circ_30272,RMVar_hsa_circ_300642,RMVar_hsa_circ_148112 4516 RMVar_ID_4516 Human_SNP_ID_455520439 A-to-I Human chr11 + 9584335 9584335 9584335 TTTAATTTTTTTCTTTTTCTTTTTGTAGAGACAGGGTCTCACTATCTTGCCCAGGCTGGTCTCGA TTTAATTTTTTTCTTTTTCTTTTTGTAGAGACGGGGTCTCACTATCTTGCCCAGGCTGGTCTCGA A G WEE1 Ensembl:ENSG00000166483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs955579174 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11758375 RMVar_hsa_circ_94359,RMVar_hsa_circ_30272,RMVar_hsa_circ_300642,RMVar_hsa_circ_148112 4517 RMVar_ID_4517 Human_SNP_ID_455520457 A-to-I Human chr11 + 9584411 9584411 9584411 TAGGTAATCCTCCTACCTCAGCCTTTCAAAGCACTGGGATTACAGGCTTGAGCCACCATACCTGG TAGGTAATCCTCCTACCTCAGCCTTTCAAAGCTCTGGGATTACAGGCTTGAGCCACCATACCTGG A T WEE1 Ensembl:ENSG00000166483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1242319651 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24919555 RMVar_hsa_circ_94359,RMVar_hsa_circ_30272,RMVar_hsa_circ_300642,RMVar_hsa_circ_148112 4518 RMVar_ID_4518 Human_SNP_ID_455520577 A-to-I Human chr11 + 9584978 9584978 9584978 CCTGTAGTCCCAGCTACTCAGGAGGTTGAATGAAGCATGAGAATTGCTTGAACCTTGTTGCAGTG CCTGTAGTCCCAGCTACTCAGGAGGTTGAATGCAGCATGAGAATTGCTTGAACCTTGTTGCAGTG A C WEE1 Ensembl:ENSG00000166483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1295292358 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94359,RMVar_hsa_circ_30272,RMVar_hsa_circ_300642,RMVar_hsa_circ_148112 4519 RMVar_ID_4519 Human_SNP_ID_455553247 A-to-I Human chr11 + 9712515 9712515 9712515 TAGGAGTTTGAGACCAGCCTGGGCAATATAGCAAGACCTCATCTCTATTTATTTTTTAAATTAAT TAGGAGTTTGAGACCAGCCTGGGCAATATAGCGAGACCTCATCTCTATTTATTTTTTAAATTAAT A G SWAP70 Ensembl:ENSG00000133789 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1196347258 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22632,RMVar_hsa_circ_65778,RMVar_hsa_circ_361192 4520 RMVar_ID_4520 Human_SNP_ID_455582389 A-to-I Human chr11 - 9831287 9831287 9831287 GTATGTTAGAACATAAGAAGGGGCCAGGTGCAATGGCTCATGCCTGTAGTCCCAGCTACTTGGAA GTATGTTAGAACATAAGAAGGGGCCAGGTGCAGTGGCTCATGCCTGTAGTCCCAGCTACTTGGAA T C SBF2 Ensembl:ENSG00000133812 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs937995442 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91477,RMVar_hsa_circ_266277,RMVar_hsa_circ_148124,RMVar_hsa_circ_94571,RMVar_hsa_circ_304499,RMVar_hsa_circ_118501,RMVar_hsa_circ_148126,RMVar_hsa_circ_148128,RMVar_hsa_circ_320496,RMVar_hsa_circ_10524,RMVar_hsa_circ_330341,RMVar_hsa_circ_297660,RMVar_hsa_circ_148133,RMVar_hsa_circ_148134,RMVar_hsa_circ_79433,RMVar_hsa_circ_148136,RMVar_hsa_circ_316164,RMVar_hsa_circ_38103,RMVar_hsa_circ_322397,RMVar_hsa_circ_148138,RMVar_hsa_circ_76380,RMVar_hsa_circ_148137,RMVar_hsa_circ_349568,RMVar_hsa_circ_123216,RMVar_hsa_circ_303694,RMVar_hsa_circ_100032,RMVar_hsa_circ_2402,RMVar_hsa_circ_4481,RMVar_hsa_circ_148139,RMVar_hsa_circ_148140 4521 RMVar_ID_4521 Human_SNP_ID_455583601 A-to-I Human chr11 - 9835448 9835448 9835448 CTTTTTATTTTATTTATTTATTTTTGTAGAGAAGAGGTCTCACTATGTTGCCCAGGCTGGTCTCA CTTTTTATTTTATTTATTTATTTTTGTAGAGATGAGGTCTCACTATGTTGCCCAGGCTGGTCTCA T A SBF2 Ensembl:ENSG00000133812 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs931135265 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91477,RMVar_hsa_circ_148124,RMVar_hsa_circ_94571,RMVar_hsa_circ_118501,RMVar_hsa_circ_148126,RMVar_hsa_circ_148128,RMVar_hsa_circ_10524,RMVar_hsa_circ_297660,RMVar_hsa_circ_148134,RMVar_hsa_circ_79433,RMVar_hsa_circ_38103,RMVar_hsa_circ_148138,RMVar_hsa_circ_76380,RMVar_hsa_circ_148137,RMVar_hsa_circ_349568,RMVar_hsa_circ_123216,RMVar_hsa_circ_303694,RMVar_hsa_circ_100032,RMVar_hsa_circ_72355,RMVar_hsa_circ_2402,RMVar_hsa_circ_4481,RMVar_hsa_circ_148139,RMVar_hsa_circ_148140,RMVar_hsa_circ_52466 4522 RMVar_ID_4522 Human_SNP_ID_455625687 A-to-I Human chr11 - 9995718 9995718 9995718 TGAACCCAGGAGGCGGAGGTCGCAGTGAGCCGAGATCACGCCGTTGCACTCCAGCCTGGACAACA TGAACCCAGGAGGCGGAGGTCGCAGTGAGCCGGGATCACGCCGTTGCACTCCAGCCTGGACAACA T C SBF2 Ensembl:ENSG00000133812 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264991077 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114274,RMVar_hsa_circ_148144,RMVar_hsa_circ_101175,RMVar_hsa_circ_148148,RMVar_hsa_circ_360812,RMVar_hsa_circ_87038,RMVar_hsa_circ_27200,RMVar_hsa_circ_148152,RMVar_hsa_circ_148153,RMVar_hsa_circ_73492,RMVar_hsa_circ_289181,RMVar_hsa_circ_325938,RMVar_hsa_circ_347503,RMVar_hsa_circ_285707,RMVar_hsa_circ_148155,RMVar_hsa_circ_148156,RMVar_hsa_circ_148154,RMVar_hsa_circ_64922,RMVar_hsa_circ_148162,RMVar_hsa_circ_345258,RMVar_hsa_circ_22929,RMVar_hsa_circ_339316,RMVar_hsa_circ_274698,RMVar_hsa_circ_148164,RMVar_hsa_circ_42593,RMVar_hsa_circ_148163,RMVar_hsa_circ_148165,RMVar_hsa_circ_277967,RMVar_hsa_circ_325882,RMVar_hsa_circ_368949,RMVar_hsa_circ_304232,RMVar_hsa_circ_18200,RMVar_hsa_circ_148168,RMVar_hsa_circ_148169,RMVar_hsa_circ_148167,RMVar_hsa_circ_101028,RMVar_hsa_circ_19428,RMVar_hsa_circ_56015,RMVar_hsa_circ_148170,RMVar_hsa_circ_35503,RMVar_hsa_circ_269710 4523 RMVar_ID_4523 Human_SNP_ID_455625697 A-to-I Human chr11 - 9995743 9995743 9995743 CAGGAGGTGAGACAGGAGGCTCACTTGAACCCAGGAGGCGGAGGTCGCAGTGAGCCGAGATCACG CAGGAGGTGAGACAGGAGGCTCACTTGAACCCGGGAGGCGGAGGTCGCAGTGAGCCGAGATCACG T C SBF2 Ensembl:ENSG00000133812 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs748147617 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114274,RMVar_hsa_circ_148144,RMVar_hsa_circ_101175,RMVar_hsa_circ_148148,RMVar_hsa_circ_360812,RMVar_hsa_circ_87038,RMVar_hsa_circ_27200,RMVar_hsa_circ_148152,RMVar_hsa_circ_148153,RMVar_hsa_circ_73492,RMVar_hsa_circ_289181,RMVar_hsa_circ_325938,RMVar_hsa_circ_347503,RMVar_hsa_circ_285707,RMVar_hsa_circ_148155,RMVar_hsa_circ_148156,RMVar_hsa_circ_148154,RMVar_hsa_circ_64922,RMVar_hsa_circ_148162,RMVar_hsa_circ_345258,RMVar_hsa_circ_22929,RMVar_hsa_circ_339316,RMVar_hsa_circ_274698,RMVar_hsa_circ_148164,RMVar_hsa_circ_42593,RMVar_hsa_circ_148163,RMVar_hsa_circ_148165,RMVar_hsa_circ_277967,RMVar_hsa_circ_325882,RMVar_hsa_circ_368949,RMVar_hsa_circ_304232,RMVar_hsa_circ_18200,RMVar_hsa_circ_148168,RMVar_hsa_circ_148169,RMVar_hsa_circ_148167,RMVar_hsa_circ_101028,RMVar_hsa_circ_19428,RMVar_hsa_circ_56015,RMVar_hsa_circ_148170,RMVar_hsa_circ_35503,RMVar_hsa_circ_269710 4524 RMVar_ID_4524 Human_SNP_ID_455633918 A-to-I Human chr11 - 10028200 10028200 10028200 GACTTTTAGAAAGTGGATGGGACGGGTGTGGTAGCTCATGCCTGTAATCACAGTACTTTGGGAGG GACTTTTAGAAAGTGGATGGGACGGGTGTGGTGGCTCATGCCTGTAATCACAGTACTTTGGGAGG T C SBF2 Ensembl:ENSG00000133812 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1565149911 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101175,RMVar_hsa_circ_14656,RMVar_hsa_circ_148148,RMVar_hsa_circ_360812,RMVar_hsa_circ_87038,RMVar_hsa_circ_148152,RMVar_hsa_circ_148153,RMVar_hsa_circ_73492,RMVar_hsa_circ_325938,RMVar_hsa_circ_285707,RMVar_hsa_circ_148155,RMVar_hsa_circ_148154,RMVar_hsa_circ_42593,RMVar_hsa_circ_325882,RMVar_hsa_circ_368949,RMVar_hsa_circ_18200,RMVar_hsa_circ_148169,RMVar_hsa_circ_19428,RMVar_hsa_circ_56015,RMVar_hsa_circ_40152,RMVar_hsa_circ_269710,RMVar_hsa_circ_95817,RMVar_hsa_circ_112635,RMVar_hsa_circ_116839,RMVar_hsa_circ_96817,RMVar_hsa_circ_148174,RMVar_hsa_circ_148176,RMVar_hsa_circ_148177,RMVar_hsa_circ_148175 4525 RMVar_ID_4525 Human_SNP_ID_455674493 A-to-I Human chr11 - 10186417 10186417 10186417 AGCGATCTCCTGCCTCAGTGTCCAGAATAGCTAGGACTACAGGTGTGTGCCACCATGCCCAGCTA AGCGATCTCCTGCCTCAGTGTCCAGAATAGCTGGGACTACAGGTGTGTGCCACCATGCCCAGCTA T C SBF2 Ensembl:ENSG00000133812 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs918863705 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_360812,RMVar_hsa_circ_148153,RMVar_hsa_circ_42593,RMVar_hsa_circ_19428,RMVar_hsa_circ_40152,RMVar_hsa_circ_117770,RMVar_hsa_circ_95817,RMVar_hsa_circ_112635,RMVar_hsa_circ_148176,RMVar_hsa_circ_148177,RMVar_hsa_circ_287161,RMVar_hsa_circ_148180,RMVar_hsa_circ_148181,RMVar_hsa_circ_358975 4526 RMVar_ID_4526 Human_SNP_ID_455693427 A-to-I Human chr11 - 10257938 10257938 10257938 TTATTTTTATTTTTTTGAGACAGTCTTGCTCTATCACCCAGGCTGGAGTGCACTGGCGCGATCTC TTATTTTTATTTTTTTGAGACAGTCTTGCTCTGTCACCCAGGCTGGAGTGCACTGGCGCGATCTC T C SBF2 Ensembl:ENSG00000133812 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049207752 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117770,RMVar_hsa_circ_95817,RMVar_hsa_circ_148177,RMVar_hsa_circ_148181 4527 RMVar_ID_4527 Human_SNP_ID_455693597 A-to-I Human chr11 - 10258363 10258363 10258363 GGCTTATGCCTGTAAATCCCAGCACTTTGGGAAGCCACAGTGGGAGGTTTGTTTGAGGCTGGGAG GGCTTATGCCTGTAAATCCCAGCACTTTGGGACGCCACAGTGGGAGGTTTGTTTGAGGCTGGGAG T G SBF2 Ensembl:ENSG00000133812 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs553277508 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117770,RMVar_hsa_circ_95817,RMVar_hsa_circ_148177,RMVar_hsa_circ_148181 4528 RMVar_ID_4528 Human_SNP_ID_455723650 A-to-I Human chr11 + 10377736 10377736 10377736 AAAACCCAGTCTCTACCAAAAATACAAAAATTAGCCAGGTGTGGTGGCACGTGTCTGTGGTCCCC AAAACCCAGTCTCTACCAAAAATACAAAAATTGGCCAGGTGTGGTGGCACGTGTCTGTGGTCCCC A G AMPD3 Ensembl:ENSG00000133805 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027381352 Functional Loss SNV dbSNP153 33..33 33 - - - 4529 RMVar_ID_4529 Human_SNP_ID_455818017 A-to-I Human chr11 + 10763230 10763230 10763230 GTTATGTGACCTTAGACTAACCACAGTGCTTTACTCTTTCTGGCTGTAGAAACATACTCCCCTTT GTTATGTGACCTTAGACTAACCACAGTGCTTTGCTCTTTCTGGCTGTAGAAACATACTCCCCTTT A G CTR9 Ensembl:ENSG00000198730 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1243060682 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25857,RMVar_hsa_circ_27958,RMVar_hsa_circ_42246,RMVar_hsa_circ_57912,RMVar_hsa_circ_107308,RMVar_hsa_circ_148189 4530 RMVar_ID_4530 Human_SNP_ID_455822025 A-to-I Human chr11 + 10778891 10778891 10778891 AAAGAGAAGGCCCTCCGGTTCTGAGCAGTCTGACAATGAATCTGTGCAGTCAGGGAGAAGCCACT AAAGAGAAGGCCCTCCGGTTCTGAGCAGTCTGGCAATGAATCTGTGCAGTCAGGGAGAAGCCACT A G CTR9 Ensembl:ENSG00000198730 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs201305345 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_1774955,Human_RBP_ID_11514005 RMVar_hsa_circ_117326,RMVar_hsa_circ_107308,RMVar_hsa_circ_148189,RMVar_hsa_circ_148191,RMVar_hsa_circ_148192,RMVar_hsa_circ_101349 4531 RMVar_ID_4531 Human_SNP_ID_455828590 A-to-I Human chr11 - 10802345 10802345 10802345 TGGAGGGACCGTTCATGCCACCCAGGATGAAAATGGATAGGGACCCACTTGGAGGACTTGCTGAT TGGAGGGACCGTTCATGCCACCCAGGATGAAAGTGGATAGGGACCCACTTGGAGGACTTGCTGAT T C EIF4G2 Ensembl:ENSG00000110321 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1564982933 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_29920,Human_RBP_ID_807845,Human_RBP_ID_1453849,Human_RBP_ID_1775148,Human_RBP_ID_2248533,Human_RBP_ID_3367643,Human_RBP_ID_6041085,Human_RBP_ID_8344082,Human_RBP_ID_8766494,Human_RBP_ID_11516571,Human_RBP_ID_17230796,Human_RBP_ID_17347263,Human_RBP_ID_17805528,Human_RBP_ID_18602598,Human_RBP_ID_22379032,Human_RBP_ID_22789567,Human_RBP_ID_22895936,Human_RBP_ID_24866686,Human_RBP_ID_26602258,Human_RBP_ID_26885371,Human_RBP_ID_27614282 Human_Splice_Rec_1210516,Human_Splice_Rec_1210517,Human_Splice_Rec_1210556,Human_Splice_Rec_1210557,Human_Splice_Rec_1210588,Human_Splice_Rec_1210589,Human_Splice_Rec_1210626,Human_Splice_Rec_1210627,Human_Splice_Rec_1210668,Human_Splice_Rec_1210669,Human_Splice_Rec_1210687,Human_Splice_Rec_1210742,Human_Splice_Rec_1210743,Human_Splice_Rec_1210752,Human_Splice_Rec_1210753 RMVar_hsa_circ_14234,RMVar_hsa_circ_56780,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_314342,RMVar_hsa_circ_148203,RMVar_hsa_circ_13727,RMVar_hsa_circ_311523,RMVar_hsa_circ_46090,RMVar_hsa_circ_362635,RMVar_hsa_circ_148204,RMVar_hsa_circ_301121,RMVar_hsa_circ_13240,RMVar_hsa_circ_148205,RMVar_hsa_circ_110537,RMVar_hsa_circ_47004,RMVar_hsa_circ_15704,RMVar_hsa_circ_29177,RMVar_hsa_circ_148208,RMVar_hsa_circ_346519,RMVar_hsa_circ_374422,RMVar_hsa_circ_326437,RMVar_hsa_circ_67139,RMVar_hsa_circ_148209,RMVar_hsa_circ_148210,RMVar_hsa_circ_116957,RMVar_hsa_circ_148212,RMVar_hsa_circ_117426,RMVar_hsa_circ_370220,RMVar_hsa_circ_148213,RMVar_hsa_circ_351499,RMVar_hsa_circ_312291,RMVar_hsa_circ_53958,RMVar_hsa_circ_103847,RMVar_hsa_circ_26531,RMVar_hsa_circ_125018,RMVar_hsa_circ_148215,RMVar_hsa_circ_7310,RMVar_hsa_circ_148216,RMVar_hsa_circ_148214,RMVar_hsa_circ_148217,RMVar_hsa_circ_50683 4532 RMVar_ID_4532 Human_SNP_ID_455831891 A-to-I Human chr11 + 10811930 10811930 10811930 TACAAAAATTAGCCTGTGTCCCACATGCCTGTAGTACCAGCTACTTGGGAGGCTGAGGCAGTAGG TACAAAAATTAGCCTGTGTCCCACATGCCTGTGGTACCAGCTACTTGGGAGGCTGAGGCAGTAGG A G AC116535.2 Ensembl:ENSG00000246308 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1396908439 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1160860 4533 RMVar_ID_4533 Human_SNP_ID_455832493 A-to-I Human chr11 + 10814487 10814487 10814487 GTAAACAATGGAGGAAAAACTATTCTGAATATATTAAACTTGAAATGCCTATTAGATATTCAAAG GTAAACAATGGAGGAAAAACTATTCTGAATATGTTAAACTTGAAATGCCTATTAGATATTCAAAG A G AC116535.2 Ensembl:ENSG00000246308 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1402770624 Functional Loss SNV dbSNP153 33..33 33 - - - 4534 RMVar_ID_4534 Human_SNP_ID_455963665 A-to-I Human chr11 - 11322854 11322854 11322854 GCAAGCCAGGAAGTAGTTCCTAAGCAGAAACTAAATTGACCAGCATCTTGATCTTGGACTTCCCA GCAAGCCAGGAAGTAGTTCCTAAGCAGAAACTGAATTGACCAGCATCTTGATCTTGGACTTCCCA T C GALNT18 Ensembl:ENSG00000110328 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs774298244 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121019,RMVar_hsa_circ_148228,RMVar_hsa_circ_90658,RMVar_hsa_circ_148227,RMVar_hsa_circ_367684,RMVar_hsa_circ_148229 4535 RMVar_ID_4535 Human_SNP_ID_455981427 A-to-I Human chr11 - 11392375 11392375 11392375 CCTCGGGTGATCTGCCTGCCTCGGCCTCCCAGAGTGCTGGGATTACAGGCTAAATGGTGACTTTT CCTCGGGTGATCTGCCTGCCTCGGCCTCCCAGTGTGCTGGGATTACAGGCTAAATGGTGACTTTT T A GALNT18 Ensembl:ENSG00000110328 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1327886256 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121019,RMVar_hsa_circ_148228,RMVar_hsa_circ_113446,RMVar_hsa_circ_148233,RMVar_hsa_circ_268095,RMVar_hsa_circ_20452,RMVar_hsa_circ_297841,RMVar_hsa_circ_148236,RMVar_hsa_circ_148237 4536 RMVar_ID_4536 Human_SNP_ID_456105378 A-to-I Human chr11 + 11905695 11905695 11905695 GTCATTCCTGCATTTAAATTAGCAAGATCTAGAAGATTTTTGACCCTTCAGTGAGTCCTAATAGT GTCATTCCTGCATTTAAATTAGCAAGATCTAGGAGATTTTTGACCCTTCAGTGAGTCCTAATAGT A G USP47 Ensembl:ENSG00000170242 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1026637060 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17560282 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 4537 RMVar_ID_4537 Human_SNP_ID_456105384 A-to-I Human chr11 + 11905722 11905722 11905722 TCTAGAAGATTTTTGACCCTTCAGTGAGTCCTAATAGTGCATGTATTATAAGAGAGAAAGTGAAT TCTAGAAGATTTTTGACCCTTCAGTGAGTCCTGATAGTGCATGTATTATAAGAGAGAAAGTGAAT A G USP47 Ensembl:ENSG00000170242 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1432720102 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17560282,Human_RBP_ID_23490072 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 4538 RMVar_ID_4538 Human_SNP_ID_456105796 A-to-I Human chr11 + 11907822 11907822 11907822 TTTAATATATTAGATATAGACGTAGGCTGGGCATAGTGGCTCACACCTGTAATCCCAGCACTTTA TTTAATATATTAGATATAGACGTAGGCTGGGCGTAGTGGCTCACACCTGTAATCCCAGCACTTTA A G USP47 Ensembl:ENSG00000170242 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1444285031 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227004,Human_RBP_ID_11543099 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 4539 RMVar_ID_4539 Human_SNP_ID_456252576 A-to-I Human chr11 + 12491232 12491232 12491232 TTACCCAGGCTGGAGTACAGTGGCACAATCACAGCCGACTGTAGCCTCTACCTCCCAGGCTCAAA TTACCCAGGCTGGAGTACAGTGGCACAATCACGGCCGACTGTAGCCTCTACCTCCCAGGCTCAAA A G PARVA Ensembl:ENSG00000197702 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1416246771 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27374,RMVar_hsa_circ_48335,RMVar_hsa_circ_367395 4540 RMVar_ID_4540 Human_SNP_ID_456307946 A-to-I Human chr11 + 12709614 12709614 12709614 GTGATCGTAGCCCACTGTGTCCTTGAACTCATAGGCTCAAGTTATCCTCAGCTCCCCCAAGTAGC GTGATCGTAGCCCACTGTGTCCTTGAACTCATGGGCTCAAGTTATCCTCAGCTCCCCCAAGTAGC A G TEAD1 Ensembl:ENSG00000187079 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1012721779 Functional Loss SNV dbSNP153 33..33 33 - - - 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 4541 RMVar_ID_4541 Human_SNP_ID_456308062 A-to-I Human chr11 + 12710056 12710056 12710056 AAAAAAAAAAATGGAATTGTAGGCCAGGCACTATGGCTCACACCTGTAATCCTAGCACTTTGGAA AAAAAAAAAAATGGAATTGTAGGCCAGGCACTGTGGCTCACACCTGTAATCCTAGCACTTTGGAA A G TEAD1 Ensembl:ENSG00000187079 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1203271664 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11556285 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 4542 RMVar_ID_4542 Human_SNP_ID_456340138 A-to-I Human chr11 + 12835449 12835449 12835449 CTGCAGCTTCAGCCTCCCAAGTAGGTGGAATTATAGGCTCGTGCCAGCACACCCGGCTAATTTTT CTGCAGCTTCAGCCTCCCAAGTAGGTGGAATTGTAGGCTCGTGCCAGCACACCCGGCTAATTTTT A G TEAD1 Ensembl:ENSG00000187079 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1273724936 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 4543 RMVar_ID_4543 Human_SNP_ID_456343789 A-to-I Human chr11 + 12848759 12848759 12848759 CTTGAGGCCAGTAGTTCAAAACCAGCATGGGCAACACAGTGAGACCCCATCTCTACAAAAAATTA CTTGAGGCCAGTAGTTCAAAACCAGCATGGGCGACACAGTGAGACCCCATCTCTACAAAAAATTA A G TEAD1 Ensembl:ENSG00000187079 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1234893091 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 4544 RMVar_ID_4544 Human_SNP_ID_456351356 A-to-I Human chr11 + 12877579 12877579 12877579 TACTCAGGAGGCTGAGGTAGGAGAATCACTTGAACCTGGGAAGCGGAGGTTGCAATGAGCTGAGA TACTCAGGAGGCTGAGGTAGGAGAATCACTTGCACCTGGGAAGCGGAGGTTGCAATGAGCTGAGA A C TEAD1 Ensembl:ENSG00000187079 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1334132686 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_319151,RMVar_hsa_circ_371690,RMVar_hsa_circ_328680,RMVar_hsa_circ_93021,RMVar_hsa_circ_567,RMVar_hsa_circ_148284,RMVar_hsa_circ_148288,RMVar_hsa_circ_77799,RMVar_hsa_circ_81685,RMVar_hsa_circ_148289,RMVar_hsa_circ_148286,RMVar_hsa_circ_148287,RMVar_hsa_circ_148285,RMVar_hsa_circ_343891,RMVar_hsa_circ_148283,RMVar_hsa_circ_378295,RMVar_hsa_circ_55572,RMVar_hsa_circ_148295,RMVar_hsa_circ_6416 4545 RMVar_ID_4545 Human_SNP_ID_456371991 A-to-I Human chr11 - 12958357 12958357 12958357 ACAAAATACAAAAATTAGCCTGGAGCATATCTATAGTTCCAGCTACTCAGGGGGCTGAGGTGGGA ACAAAATACAAAAATTAGCCTGGAGCATATCTGTAGTTCCAGCTACTCAGGGGGCTGAGGTGGGA T C LINC00958 RNACentral:URS00009BE47B lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569920633 Functional Loss SNV dbSNP153 33..33 33 - - - 4546 RMVar_ID_4546 Human_SNP_ID_456372098 A-to-I Human chr11 - 12958931 12958931 12958931 TTACCCAGGCTGGTCTCAAACTTCTGGACTCAAGCAATCCTCCCTCCTCGGCCTGTAATTATTTC TTACCCAGGCTGGTCTCAAACTTCTGGACTCAGGCAATCCTCCCTCCTCGGCCTGTAATTATTTC T C LINC00958 RNACentral:URS00009BE47B lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1250619409 Functional Loss SNV dbSNP153 33..33 33 - - - 4547 RMVar_ID_4547 Human_SNP_ID_456372440 A-to-I Human chr11 - 12960330 12960330 12960330 CAACAATTAGCTGAGCATGGTGGTGCACACCTATGGTCCTAGCTACTAGGAGGCTGAGGTGGGAG CAACAATTAGCTGAGCATGGTGGTGCACACCTGTGGTCCTAGCTACTAGGAGGCTGAGGTGGGAG T C LINC00958,LINC00958:2 RNACentral:URS00009BE47B,RNACentral:URS00008B7DF5 lincRNA,lincRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005332260 Functional Loss SNV dbSNP153 33..33 33 - - - 4548 RMVar_ID_4548 Human_SNP_ID_456372870 A-to-I Human chr11 - 12962176 12962176 12962176 TCATCTTCCTGTGTTGCCCAGGCTTGTCTCAAACTCCTGGGCTCAAGTGATCCTCTCACCTCAGC TCATCTTCCTGTGTTGCCCAGGCTTGTCTCAATCTCCTGGGCTCAAGTGATCCTCTCACCTCAGC T A LINC00958 Ensembl:ENSG00000251381 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs905454907 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11561234 4549 RMVar_ID_4549 Human_SNP_ID_456378932 A-to-I Human chr11 - 12988279 12988279 12988279 CTGTGGTCCCAGCTACATGGGAGGCTGAGCCAAGAGGATCTCTTGAGGCCAGGAGGTTGAGGCTG CTGTGGTCCCAGCTACATGGGAGGCTGAGCCAGGAGGATCTCTTGAGGCCAGGAGGTTGAGGCTG T C LINC00958 Ensembl:ENSG00000251381 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1241768506 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75877,RMVar_hsa_circ_148302 4550 RMVar_ID_4550 Human_SNP_ID_456428406 A-to-I Human chr11 - 13179480 13179480 13179480 TTGCCCAGGCTGGAGTGAACCAGCATGATCTCAGTTGACTACAATCTGCGCCTCTCAGCCTCAAG TTGCCCAGGCTGGAGTGAACCAGCATGATCTCTGTTGACTACAATCTGCGCCTCTCAGCCTCAAG T A HSALNG0082761 RNACentral:URS0000E9AA7C lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs553960829 Functional Loss SNV dbSNP153 33..33 33 - - - 4551 RMVar_ID_4551 Human_SNP_ID_456486292 A-to-I Human chr11 - 13412662 13412662 13412662 AGAGTAGATAGTATTGTTTTGGGGAATTATTTATATCTTCCATAGTGCCCAGGATATCATCCTAC AGAGTAGATAGTATTGTTTTGGGGAATTATTTGTATCTTCCATAGTGCCCAGGATATCATCCTAC T C BTBD10 Ensembl:ENSG00000148925 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1565240576 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28620,RMVar_hsa_circ_273865,RMVar_hsa_circ_276822,RMVar_hsa_circ_368178,RMVar_hsa_circ_269321,RMVar_hsa_circ_148312,RMVar_hsa_circ_148313,RMVar_hsa_circ_267339,RMVar_hsa_circ_314631,RMVar_hsa_circ_148314 4552 RMVar_ID_4552 Human_SNP_ID_456560694 A-to-I Human chr11 + 13703219 13703219 13703219 TTTGTTTTTGTTTGAGATAGGGTCTCACCTTTATCGCCCAGGCTGAGAGTGCAGTGACACAATCA TTTGTTTTTGTTTGAGATAGGGTCTCACCTTTGTCGCCCAGGCTGAGAGTGCAGTGACACAATCA A G FAR1 Ensembl:ENSG00000197601 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1382827483 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6057483,Human_RBP_ID_11568250,Human_RBP_ID_23495219 RMVar_hsa_circ_22865,RMVar_hsa_circ_86150,RMVar_hsa_circ_368689,RMVar_hsa_circ_148324,RMVar_hsa_circ_322498,RMVar_hsa_circ_94412,RMVar_hsa_circ_148325 4553 RMVar_ID_4553 Human_SNP_ID_456560877 A-to-I Human chr11 + 13703923 13703923 13703923 AAAATGAGCCGGGCATGGTGGCACACGCCTGTAATCTCAGCTGCTTGGGAGGTTGAGGCAGAAGA AAAATGAGCCGGGCATGGTGGCACACGCCTGTCATCTCAGCTGCTTGGGAGGTTGAGGCAGAAGA A C FAR1 Ensembl:ENSG00000197601 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1481790579 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22865,RMVar_hsa_circ_86150,RMVar_hsa_circ_368689,RMVar_hsa_circ_148324,RMVar_hsa_circ_322498,RMVar_hsa_circ_94412,RMVar_hsa_circ_148325 4554 RMVar_ID_4554 Human_SNP_ID_456703444 A-to-I Human chr11 - 14276397 14276397 14276397 TTGTGTAGAGATGAGGTCTTGCCCTGTTGCCTAAGCTGGTCTCAAACTCCTGGACTCAAGCTGTC TTGTGTAGAGATGAGGTCTTGCCCTGTTGCCTCAGCTGGTCTCAAACTCCTGGACTCAAGCTGTC T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991108518 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1161457,Human_RBP_ID_11570081 4555 RMVar_ID_4555 Human_SNP_ID_456703498 A-to-I Human chr11 - 14276554 14276554 14276554 AGACAAGGTCTTGATCTGTTGCCCAGGTTGGCATGTAGTGGCGCCATCTTGGCTCACTGCAACCT AGACAAGGTCTTGATCTGTTGCCCAGGTTGGCGTGTAGTGGCGCCATCTTGGCTCACTGCAACCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs868921936 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1161460,Human_RBP_ID_11570087,Human_RBP_ID_19614797,Human_RBP_ID_23495612,Human_RBP_ID_24876775 4556 RMVar_ID_4556 Human_SNP_ID_456703770 A-to-I Human chr11 - 14277444 14277444 14277444 ACCAACATGATGAAACCCCATCTCTACTAAAAATACAAAAATTAGCTGGGTGTGGTGGCGGGTGC ACCAACATGATGAAACCCCATCTCTACTAAAACTACAAAAATTAGCTGGGTGTGGTGGCGGGTGC T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264109416 Functional Loss SNV dbSNP153 33..33 33 - - - 4557 RMVar_ID_4557 Human_SNP_ID_456703794 A-to-I Human chr11 - 14277540 14277540 14277540 TAATTGTCTGGGTGCAGTGGCGCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGTGGA TAATTGTCTGGGTGCAGTGGCGCACACCTGTAGTCCCAGCACTTTGGGAGGCTGAGGCAGGTGGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1196091564 Functional Loss SNV dbSNP153 33..33 33 - - - 4558 RMVar_ID_4558 Human_SNP_ID_456712429 A-to-I Human chr11 - 14311586 14311586 14311586 GAGGTGGGCGGATCACCCGAGATCAGGAATTCAAGACCAGCCTGGCCAACATGGTGAAACCCCGT GAGGTGGGCGGATCACCCGAGATCAGGAATTCGAGACCAGCCTGGCCAACATGGTGAAACCCCGT T C RRAS2 Ensembl:ENSG00000133818 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350706388 Functional Loss SNV dbSNP153 33..33 33 - - - 4559 RMVar_ID_4559 Human_SNP_ID_456712430 A-to-I Human chr11 - 14311590 14311590 14311590 GGCTGAGGTGGGCGGATCACCCGAGATCAGGAATTCAAGACCAGCCTGGCCAACATGGTGAAACC GGCTGAGGTGGGCGGATCACCCGAGATCAGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACC T C RRAS2 Ensembl:ENSG00000133818 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1309362849 Functional Loss SNV dbSNP153 33..33 33 - - - 4560 RMVar_ID_4560 Human_SNP_ID_456752204 A-to-I Human chr11 - 14478731 14478731 14478731 TAAAGAATTGTTGGCTGGGTATGGTGGCTCACACTTGTATTCCCAGCACTTTGGGAGGCCAAGGC TAAAGAATTGTTGGCTGGGTATGGTGGCTCACGCTTGTATTCCCAGCACTTTGGGAGGCCAAGGC T C COPB1 Ensembl:ENSG00000129083 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1478417914 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24877037 RMVar_hsa_circ_351486,RMVar_hsa_circ_66374,RMVar_hsa_circ_148334,RMVar_hsa_circ_58168,RMVar_hsa_circ_348044,RMVar_hsa_circ_148339,RMVar_hsa_circ_90582,RMVar_hsa_circ_21318,RMVar_hsa_circ_22526,RMVar_hsa_circ_3028,RMVar_hsa_circ_148342,RMVar_hsa_circ_342729,RMVar_hsa_circ_360951,RMVar_hsa_circ_50738,RMVar_hsa_circ_68851,RMVar_hsa_circ_11113 4561 RMVar_ID_4561 Human_SNP_ID_456753868 A-to-I Human chr11 - 14485370 14485370 14485370 TTAAAACCAGGAGTTTGAGACCAGCCTGGGCAACAAAGAGAGACTCTATCTGTACAGAACCTTTT TTAAAACCAGGAGTTTGAGACCAGCCTGGGCAGCAAAGAGAGACTCTATCTGTACAGAACCTTTT T C COPB1 Ensembl:ENSG00000129083 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1185123250 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_351486,RMVar_hsa_circ_66374,RMVar_hsa_circ_148334,RMVar_hsa_circ_348044,RMVar_hsa_circ_148339,RMVar_hsa_circ_21318,RMVar_hsa_circ_360951,RMVar_hsa_circ_50738,RMVar_hsa_circ_11113,RMVar_hsa_circ_303804,RMVar_hsa_circ_52139,RMVar_hsa_circ_347366 4562 RMVar_ID_4562 Human_SNP_ID_456755245 A-to-I Human chr11 - 14491138 14491138 14491138 CAGGAGGCTGAGGCAGGAGAATCACTCGACCTAGAAGGCGGAGGTTGCAGTAAGCCGAGATCACT CAGGAGGCTGAGGCAGGAGAATCACTCGACCTGGAAGGCGGAGGTTGCAGTAAGCCGAGATCACT T C COPB1 Ensembl:ENSG00000129083 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs891186607 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_351486,RMVar_hsa_circ_66374,RMVar_hsa_circ_148334,RMVar_hsa_circ_348044,RMVar_hsa_circ_148339,RMVar_hsa_circ_21318,RMVar_hsa_circ_360951,RMVar_hsa_circ_50738,RMVar_hsa_circ_93534,RMVar_hsa_circ_11113,RMVar_hsa_circ_303804,RMVar_hsa_circ_347366,RMVar_hsa_circ_286496,RMVar_hsa_circ_355358,RMVar_hsa_circ_353928,RMVar_hsa_circ_148344,RMVar_hsa_circ_342840,RMVar_hsa_circ_358777 4563 RMVar_ID_4563 Human_SNP_ID_456755246 A-to-I Human chr11 - 14491138 14491138 14491138 CAGGAGGCTGAGGCAGGAGAATCACTCGACCTAGAAGGCGGAGGTTGCAGTAAGCCGAGATCACT CAGGAGGCTGAGGCAGGAGAATCACTCGACCTCGAAGGCGGAGGTTGCAGTAAGCCGAGATCACT T G COPB1 Ensembl:ENSG00000129083 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs891186607 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_351486,RMVar_hsa_circ_66374,RMVar_hsa_circ_148334,RMVar_hsa_circ_348044,RMVar_hsa_circ_148339,RMVar_hsa_circ_21318,RMVar_hsa_circ_360951,RMVar_hsa_circ_50738,RMVar_hsa_circ_93534,RMVar_hsa_circ_11113,RMVar_hsa_circ_303804,RMVar_hsa_circ_347366,RMVar_hsa_circ_286496,RMVar_hsa_circ_355358,RMVar_hsa_circ_353928,RMVar_hsa_circ_148344,RMVar_hsa_circ_342840,RMVar_hsa_circ_358777 4564 RMVar_ID_4564 Human_SNP_ID_456755258 A-to-I Human chr11 - 14491177 14491174 14491177 AGCCTGGCATGGTGGCACGTGCCTGTAGTCCCAGATACTCAGGAGGCTGAGGCAGGAGAATCACT AGCCTGGCATGGTGGCACGTGCCTGTAGTCCC___TACTCAGGAGGCTGAGGCAGGAGAATCACT ATCT A COPB1 Ensembl:ENSG00000129083 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1159794390 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_351486,RMVar_hsa_circ_66374,RMVar_hsa_circ_148334,RMVar_hsa_circ_348044,RMVar_hsa_circ_148339,RMVar_hsa_circ_21318,RMVar_hsa_circ_360951,RMVar_hsa_circ_50738,RMVar_hsa_circ_93534,RMVar_hsa_circ_11113,RMVar_hsa_circ_303804,RMVar_hsa_circ_347366,RMVar_hsa_circ_286496,RMVar_hsa_circ_355358,RMVar_hsa_circ_353928,RMVar_hsa_circ_148344,RMVar_hsa_circ_342840,RMVar_hsa_circ_358777 4565 RMVar_ID_4565 Human_SNP_ID_456755260 A-to-I Human chr11 - 14491177 14491177 14491177 AGCCTGGCATGGTGGCACGTGCCTGTAGTCCCAGATACTCAGGAGGCTGAGGCAGGAGAATCACT AGCCTGGCATGGTGGCACGTGCCTGTAGTCCCGGATACTCAGGAGGCTGAGGCAGGAGAATCACT T C COPB1 Ensembl:ENSG00000129083 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1234413093 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_351486,RMVar_hsa_circ_66374,RMVar_hsa_circ_148334,RMVar_hsa_circ_348044,RMVar_hsa_circ_148339,RMVar_hsa_circ_21318,RMVar_hsa_circ_360951,RMVar_hsa_circ_50738,RMVar_hsa_circ_93534,RMVar_hsa_circ_11113,RMVar_hsa_circ_303804,RMVar_hsa_circ_347366,RMVar_hsa_circ_286496,RMVar_hsa_circ_355358,RMVar_hsa_circ_353928,RMVar_hsa_circ_148344,RMVar_hsa_circ_342840,RMVar_hsa_circ_358777 4566 RMVar_ID_4566 Human_SNP_ID_456755269 A-to-I Human chr11 - 14491201 14491201 14491201 TCTACTAAAAAAATAACAAAAATTAGCCTGGCATGGTGGCACGTGCCTGTAGTCCCAGATACTCA TCTACTAAAAAAATAACAAAAATTAGCCTGGCGTGGTGGCACGTGCCTGTAGTCCCAGATACTCA T C COPB1 Ensembl:ENSG00000129083 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1035418751 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_351486,RMVar_hsa_circ_66374,RMVar_hsa_circ_148334,RMVar_hsa_circ_348044,RMVar_hsa_circ_148339,RMVar_hsa_circ_21318,RMVar_hsa_circ_360951,RMVar_hsa_circ_50738,RMVar_hsa_circ_93534,RMVar_hsa_circ_11113,RMVar_hsa_circ_303804,RMVar_hsa_circ_347366,RMVar_hsa_circ_286496,RMVar_hsa_circ_355358,RMVar_hsa_circ_353928,RMVar_hsa_circ_148344,RMVar_hsa_circ_342840,RMVar_hsa_circ_358777 4567 RMVar_ID_4567 Human_SNP_ID_456755598 A-to-I Human chr11 - 14492429 14492429 14492429 TGAAGCAGAAGAATTGCTCGAACCTGGGAGGCAGAGGTTGCGATGAACCGAGATCGCGCTATTGC TGAAGCAGAAGAATTGCTCGAACCTGGGAGGCGGAGGTTGCGATGAACCGAGATCGCGCTATTGC T C COPB1 Ensembl:ENSG00000129083 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1024074693 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_351486,RMVar_hsa_circ_66374,RMVar_hsa_circ_148334,RMVar_hsa_circ_348044,RMVar_hsa_circ_148339,RMVar_hsa_circ_21318,RMVar_hsa_circ_360951,RMVar_hsa_circ_50738,RMVar_hsa_circ_93534,RMVar_hsa_circ_11113,RMVar_hsa_circ_303804,RMVar_hsa_circ_347366,RMVar_hsa_circ_286496,RMVar_hsa_circ_355358,RMVar_hsa_circ_353928,RMVar_hsa_circ_148344,RMVar_hsa_circ_342840,RMVar_hsa_circ_358777 4568 RMVar_ID_4568 Human_SNP_ID_456759089 A-to-I Human chr11 - 14506004 14506004 14506004 GACTAGTTTCTTTTTTGTTGTTTTTTGAGACAAGGTCTTGCCCTCTTGTCCAGGCTGGCGTGCAG GACTAGTTTCTTTTTTGTTGTTTTTTGAGACAGGGTCTTGCCCTCTTGTCCAGGCTGGCGTGCAG T C AC018523.2,PSMA1 Ensembl:ENSG00000256206,Ensembl:ENSG00000129084 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1423885771 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_148334,RMVar_hsa_circ_3278,RMVar_hsa_circ_148345,RMVar_hsa_circ_117409,RMVar_hsa_circ_148349 4569 RMVar_ID_4569 Human_SNP_ID_456759750 A-to-I Human chr11 - 14508622 14508622 14508622 CTCACATGAATTACCTGAATAGCCTTAAAACTATTTCTACCCATAGCCCCACTATCTATTTACCC CTCACATGAATTACCTGAATAGCCTTAAAACTTTTTCTACCCATAGCCCCACTATCTATTTACCC T A AC018523.2,PSMA1 Ensembl:ENSG00000256206,Ensembl:ENSG00000129084 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749275213 Functional Loss SNV dbSNP153 33..33 33 - - - 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 4570 RMVar_ID_4570 Human_SNP_ID_456759751 A-to-I Human chr11 - 14508622 14508622 14508622 CTCACATGAATTACCTGAATAGCCTTAAAACTATTTCTACCCATAGCCCCACTATCTATTTACCC CTCACATGAATTACCTGAATAGCCTTAAAACTGTTTCTACCCATAGCCCCACTATCTATTTACCC T C AC018523.2,PSMA1 Ensembl:ENSG00000256206,Ensembl:ENSG00000129084 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749275213 Functional Loss SNV dbSNP153 33..33 33 - - - 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 4571 RMVar_ID_4571 Human_SNP_ID_456759753 A-to-I Human chr11 - 14508642 14508642 14508642 TGCTCCAATCGCTATCATCTCTCACATGAATTACCTGAATAGCCTTAAAACTATTTCTACCCATA TGCTCCAATCGCTATCATCTCTCACATGAATTCCCTGAATAGCCTTAAAACTATTTCTACCCATA T G AC018523.2,PSMA1 Ensembl:ENSG00000256206,Ensembl:ENSG00000129084 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1021773274 Functional Loss SNV dbSNP153 33..33 33 - - - 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 4572 RMVar_ID_4572 Human_SNP_ID_456759759 A-to-I Human chr11 - 14508661 14508661 14508661 GACGGTCACTCTGTCACTCTGCTCCAATCGCTATCATCTCTCACATGAATTACCTGAATAGCCTT GACGGTCACTCTGTCACTCTGCTCCAATCGCTGTCATCTCTCACATGAATTACCTGAATAGCCTT T C AC018523.2,PSMA1 Ensembl:ENSG00000256206,Ensembl:ENSG00000129084 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs558660083 Functional Loss SNV dbSNP153 33..33 33 - - - 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 4573 RMVar_ID_4573 Human_SNP_ID_456761564 A-to-I Human chr11 - 14515968 14515968 14515968 TGACCTCGTGATCCACCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACAGCAC TGACCTCGTGATCCACCTGCCTCGGCCTCCCAGAGTGCTGGGATTACAGGCGTGAGCCACAGCAC T C AC018523.2,PSMA1 Ensembl:ENSG00000256206,Ensembl:ENSG00000129084 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs553911414 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3278,RMVar_hsa_circ_117409,RMVar_hsa_circ_148349,RMVar_hsa_circ_125571,RMVar_hsa_circ_72093,RMVar_hsa_circ_18949,RMVar_hsa_circ_98278,RMVar_hsa_circ_148352,RMVar_hsa_circ_148353 4574 RMVar_ID_4574 Human_SNP_ID_456761588 A-to-I Human chr11 - 14516044 14516044 14516044 CACCACACCCGGCTAATTTTTGCATTTTTAGTAGAGACGAGGTTTCACCATATTGGCCAGGCTGG CACCACACCCGGCTAATTTTTGCATTTTTAGTCGAGACGAGGTTTCACCATATTGGCCAGGCTGG T G AC018523.2,PSMA1 Ensembl:ENSG00000256206,Ensembl:ENSG00000129084 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1442924381 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3278,RMVar_hsa_circ_117409,RMVar_hsa_circ_148349,RMVar_hsa_circ_125571,RMVar_hsa_circ_72093,RMVar_hsa_circ_18949,RMVar_hsa_circ_98278,RMVar_hsa_circ_148352,RMVar_hsa_circ_148353 4575 RMVar_ID_4575 Human_SNP_ID_456770293 A-to-I Human chr11 - 14553917 14553917 14553917 CTCATATATCGCTGGTGGTAGTGTAAAATGGTATAGCCACTCTGCAAAATAGTTTGGCAATTTCT CTCATATATCGCTGGTGGTAGTGTAAAATGGTGTAGCCACTCTGCAAAATAGTTTGGCAATTTCT T C PSMA1 Ensembl:ENSG00000129084 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270547620 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1161494 RMVar_hsa_circ_98278,RMVar_hsa_circ_148352 4576 RMVar_ID_4576 Human_SNP_ID_456777837 A-to-I Human chr11 - 14586961 14586961 14586961 GGTCAGGAGATCGAGACCATCCTGGCCAACATAGTGGAACCCTGTCTCTACTAAAAATACAAAAA GGTCAGGAGATCGAGACCATCCTGGCCAACATGGTGGAACCCTGTCTCTACTAAAAATACAAAAA T C PSMA1 Ensembl:ENSG00000129084 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1258161855 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98278,RMVar_hsa_circ_148352 4577 RMVar_ID_4577 Human_SNP_ID_456782645 A-to-I Human chr11 - 14605662 14605662 14605662 GCAAAAGAAGCCAGGCACAGTAGCTCATGCCTATAATCCCAGCACTTTGGGAGGCTGAGGCAGGA GCAAAAGAAGCCAGGCACAGTAGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGA T C PSMA1 Ensembl:ENSG00000129084 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1460773168 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98278,RMVar_hsa_circ_148352 4578 RMVar_ID_4578 Human_SNP_ID_456786933 A-to-I Human chr11 - 14625365 14625365 14625365 CAGCTCACTGCAAACTTTGCCTCCCGGGTTCAAGTGATTCTCCTACCTCAGCCTCCCAAGTAGCT CAGCTCACTGCAAACTTTGCCTCCCGGGTTCAGGTGATTCTCCTACCTCAGCCTCCCAAGTAGCT T C PSMA1 Ensembl:ENSG00000129084 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs541427753 Functional Loss SNV dbSNP153 33..33 33 - - - 4579 RMVar_ID_4579 Human_SNP_ID_456786939 A-to-I Human chr11 - 14625391 14625391 14625391 CAGGCTGGAGTGCAGTGGCACAATCTCAGCTCACTGCAAACTTTGCCTCCCGGGTTCAAGTGATT CAGGCTGGAGTGCAGTGGCACAATCTCAGCTCGCTGCAAACTTTGCCTCCCGGGTTCAAGTGATT T C PSMA1 Ensembl:ENSG00000129084 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs762771431 Functional Loss SNV dbSNP153 33..33 33 - - - 4580 RMVar_ID_4580 Human_SNP_ID_456800917 A-to-I Human chr11 + 14673776 14673776 14673776 CAATTCGTACAAGTAATCTCAGGAGATGTGGCACTCCATACACCTGGGACATGGGTGCCTTGGGG CAATTCGTACAAGTAATCTCAGGAGATGTGGCGCTCCATACACCTGGGACATGGGTGCCTTGGGG A G PDE3B Ensembl:ENSG00000152270 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs570791232 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11764250 4581 RMVar_ID_4581 Human_SNP_ID_456817288 A-to-I Human chr11 + 14741218 14741218 14741218 ATATTGTCAGTGGGGTGTTACAGTCTCCCACTATTACTGTGTCGGAGTCTAAGTCTCTTTGTAGG ATATTGTCAGTGGGGTGTTACAGTCTCCCACTGTTACTGTGTCGGAGTCTAAGTCTCTTTGTAGG A G PDE3B Ensembl:ENSG00000152270 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928712632 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11573754 4582 RMVar_ID_4582 Human_SNP_ID_456834544 A-to-I Human chr11 + 14813521 14813521 14813521 AGGCATAGGACTTAGCCGTGTGTGACTCCTGTAATGACAAGAACCCTTGTCATTACATTGAGCAC AGGCATAGGACTTAGCCGTGTGTGACTCCTGTGATGACAAGAACCCTTGTCATTACATTGAGCAC A G PDE3B Ensembl:ENSG00000152270 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs563219987 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21653,RMVar_hsa_circ_295871,RMVar_hsa_circ_328672,RMVar_hsa_circ_330531,RMVar_hsa_circ_346546,RMVar_hsa_circ_268644,RMVar_hsa_circ_148356,RMVar_hsa_circ_148357,RMVar_hsa_circ_346074,RMVar_hsa_circ_148355,RMVar_hsa_circ_319887,RMVar_hsa_circ_302737,RMVar_hsa_circ_289137,RMVar_hsa_circ_36367,RMVar_hsa_circ_342346,RMVar_hsa_circ_148362,RMVar_hsa_circ_148363,RMVar_hsa_circ_148361,RMVar_hsa_circ_358644,RMVar_hsa_circ_367266,RMVar_hsa_circ_349657,RMVar_hsa_circ_282505,RMVar_hsa_circ_336220,RMVar_hsa_circ_65973,RMVar_hsa_circ_148369,RMVar_hsa_circ_313880,RMVar_hsa_circ_148364,RMVar_hsa_circ_148366,RMVar_hsa_circ_148367,RMVar_hsa_circ_148365,RMVar_hsa_circ_320020,RMVar_hsa_circ_333863,RMVar_hsa_circ_148371,RMVar_hsa_circ_8781,RMVar_hsa_circ_148370,RMVar_hsa_circ_148368 4583 RMVar_ID_4583 Human_SNP_ID_456843697 A-to-I Human chr11 + 14851106 14851106 14851106 TGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCACGCCTGGCCCTAAATACGTGGTTTT TGGCCTCCCAAAGTGCTGGGATTACAGGCGTGCGCCACCACGCCTGGCCCTAAATACGTGGTTTT A C PDE3B Ensembl:ENSG00000152270 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs927635651 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_328672,RMVar_hsa_circ_319887,RMVar_hsa_circ_148363,RMVar_hsa_circ_358644,RMVar_hsa_circ_336220,RMVar_hsa_circ_148367,RMVar_hsa_circ_148368,RMVar_hsa_circ_293889,RMVar_hsa_circ_148374,RMVar_hsa_circ_305335,RMVar_hsa_circ_102096,RMVar_hsa_circ_28473,RMVar_hsa_circ_148376,RMVar_hsa_circ_148378,RMVar_hsa_circ_148379 4584 RMVar_ID_4584 Human_SNP_ID_456852779 A-to-I Human chr11 - 14890781 14890781 14890781 CACTTTAGGAGGCCGAGGCGGGCGGATCACGAAATCAGGAGATCGAGACCGTCGTGGCTAACACG CACTTTAGGAGGCCGAGGCGGGCGGATCACGACATCAGGAGATCGAGACCGTCGTGGCTAACACG T G CYP2R1 Ensembl:ENSG00000186104 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1477345699 Functional Loss SNV dbSNP153 33..33 33 - - - 4585 RMVar_ID_4585 Human_SNP_ID_456852789 A-to-I Human chr11 - 14890807 14890807 14890807 GCGGTGGCTCACGCCTATAATCCCAGCACTTTAGGAGGCCGAGGCGGGCGGATCACGAAATCAGG GCGGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGGATCACGAAATCAGG T C CYP2R1 Ensembl:ENSG00000186104 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1033560776 Functional Loss SNV dbSNP153 33..33 33 - - - 4586 RMVar_ID_4586 Human_SNP_ID_456852792 A-to-I Human chr11 - 14890823 14890823 14890823 GTCTAGGTGCCCGGGCGCGGTGGCTCACGCCTATAATCCCAGCACTTTAGGAGGCCGAGGCGGGC GTCTAGGTGCCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTAGGAGGCCGAGGCGGGC T C CYP2R1 Ensembl:ENSG00000186104 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs959364274 Functional Loss SNV dbSNP153 33..33 33 - - - 4587 RMVar_ID_4587 Human_SNP_ID_457290094 A-to-I Human chr11 + 16740482 16740482 16740482 GTGCAGTGGCACGATCGATCAGTGCTCCCTGCAGCCTCCACCTCCCTGGCTCAGGTGATCCTCCT GTGCAGTGGCACGATCGATCAGTGCTCCCTGCGGCCTCCACCTCCCTGGCTCAGGTGATCCTCCT A G C11orf58 Ensembl:ENSG00000110696 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1139198 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1353979 4588 RMVar_ID_4588 Human_SNP_ID_457290096 A-to-I Human chr11 + 16740489 16740489 16740489 GGCACGATCGATCAGTGCTCCCTGCAGCCTCCACCTCCCTGGCTCAGGTGATCCTCCTGCTTCAA GGCACGATCGATCAGTGCTCCCTGCAGCCTCCGCCTCCCTGGCTCAGGTGATCCTCCTGCTTCAA A G C11orf58 Ensembl:ENSG00000110696 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1139200 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1353979 4589 RMVar_ID_4589 Human_SNP_ID_457290101 A-to-I Human chr11 + 16740502 16740502 16740502 AGTGCTCCCTGCAGCCTCCACCTCCCTGGCTCAGGTGATCCTCCTGCTTCAACCCCCTCTTCCCC AGTGCTCCCTGCAGCCTCCACCTCCCTGGCTCCGGTGATCCTCCTGCTTCAACCCCCTCTTCCCC A C C11orf58 Ensembl:ENSG00000110696 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1139201 Functional Loss SNV dbSNP153 33..33 33 - - - 4590 RMVar_ID_4590 Human_SNP_ID_457290102 A-to-I Human chr11 + 16740502 16740502 16740502 AGTGCTCCCTGCAGCCTCCACCTCCCTGGCTCAGGTGATCCTCCTGCTTCAACCCCCTCTTCCCC AGTGCTCCCTGCAGCCTCCACCTCCCTGGCTCGGGTGATCCTCCTGCTTCAACCCCCTCTTCCCC A G C11orf58 Ensembl:ENSG00000110696 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1139201 Functional Loss SNV dbSNP153 33..33 33 - - - 4591 RMVar_ID_4591 Human_SNP_ID_457290117 A-to-I Human chr11 + 16740560 16740560 16740560 CTTCCCCCACCACCACTACAGTAGCTCGGACTACAGGTGTGCACCATTACACCCGACTAATTTTT CTTCCCCCACCACCACTACAGTAGCTCGGACTGCAGGTGTGCACCATTACACCCGACTAATTTTT A G C11orf58 Ensembl:ENSG00000110696 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1423970033 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6059555 4592 RMVar_ID_4592 Human_SNP_ID_457290122 A-to-I Human chr11 + 16740578 16740578 16740578 CAGTAGCTCGGACTACAGGTGTGCACCATTACACCCGACTAATTTTTTGTATTTTTAGTAGAGAC CAGTAGCTCGGACTACAGGTGTGCACCATTACGCCCGACTAATTTTTTGTATTTTTAGTAGAGAC A G C11orf58 Ensembl:ENSG00000110696 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1139202 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6059556 4593 RMVar_ID_4593 Human_SNP_ID_457290126 A-to-I Human chr11 + 16740586 16740586 16740586 CGGACTACAGGTGTGCACCATTACACCCGACTAATTTTTTGTATTTTTAGTAGAGACCAGATTTT CGGACTACAGGTGTGCACCATTACACCCGACTCATTTTTTGTATTTTTAGTAGAGACCAGATTTT A C C11orf58 Ensembl:ENSG00000110696 Protein coding intron GSE38233;GSE100210;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,cerebellum - 24183664,29129909,30559470 RNA-Seq:(High) rs1042685950 Functional Loss SNV dbSNP153 33..33 33 - - - 4594 RMVar_ID_4594 Human_SNP_ID_457290127 A-to-I Human chr11 + 16740586 16740586 16740586 CGGACTACAGGTGTGCACCATTACACCCGACTAATTTTTTGTATTTTTAGTAGAGACCAGATTTT CGGACTACAGGTGTGCACCATTACACCCGACTGATTTTTTGTATTTTTAGTAGAGACCAGATTTT A G C11orf58 Ensembl:ENSG00000110696 Protein coding intron GSE38233;GSE100210;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,cerebellum - 24183664,29129909,30559470 RNA-Seq:(High) rs1042685950 Functional Loss SNV dbSNP153 33..33 33 - - - 4595 RMVar_ID_4595 Human_SNP_ID_457290150 A-to-I Human chr11 + 16740696 16740696 16740696 TGCCCACCTCGGCCTCCCAAAGTGCTGGAATTACAGGTGTGAGCCACCTCGCCCAGCCAGTACTT TGCCCACCTCGGCCTCCCAAAGTGCTGGAATTGCAGGTGTGAGCCACCTCGCCCAGCCAGTACTT A G C11orf58 Ensembl:ENSG00000110696 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1139204 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17559860 4596 RMVar_ID_4596 Human_SNP_ID_457291515 A-to-I Human chr11 + 16746753 16746753 16746753 CAGTCTCACTGCAACCTCTGCCTCCCGGGTTCAAGCAGTTCTCTGCCTCAGCCTCCCAAGTAGCT CAGTCTCACTGCAACCTCTGCCTCCCGGGTTCGAGCAGTTCTCTGCCTCAGCCTCCCAAGTAGCT A G C11orf58 Ensembl:ENSG00000110696 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1219648323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11574977 RMVar_hsa_circ_1071,RMVar_hsa_circ_358044 4597 RMVar_ID_4597 Human_SNP_ID_457293866 A-to-I Human chr11 + 16756395 16756395 16756395 AGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGTTGGGACTACAGTCATGTGCCACTACT AGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCTAGTAGTTGGGACTACAGTCATGTGCCACTACT A T C11orf58 Ensembl:ENSG00000110696 Protein coding 3'UTR GSE38233;GSE100210;GSE99789 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 24183664,29129909,29796672 RNA-Seq:(High) rs949332640 Functional Loss SNV dbSNP153 33..33 33 - - - 4598 RMVar_ID_4598 Human_SNP_ID_457293870 A-to-I Human chr11 + 16756409 16756408 16756410 CTCCTGCCTCAGCCTCCCAAGTAGTTGGGACTACAGTCATGTGCCACTACTCCTGGCTAATTTTT CTCCTGCCTCAGCCTCCCAAGTAGTTGGGACT__AGTCATGTGCCACTACTCCTGGCTAATTTTT TAC T C11orf58 Ensembl:ENSG00000110696 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1249498994 Functional Loss DEL dbSNP153 33..34 33 - - - 4599 RMVar_ID_4599 Human_SNP_ID_457293926 A-to-I Human chr11 + 16756651 16756651 16756651 GAACGTGTTGCCATGTGCGGTGGCTCACACCTATAATCCCAGCACTTTGGGAGGCCGAGGTGGCT GAACGTGTTGCCATGTGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGCT A G C11orf58 Ensembl:ENSG00000110696 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs185991654 Functional Loss SNV dbSNP153 33..33 33 - - - 4600 RMVar_ID_4600 Human_SNP_ID_457293947 A-to-I Human chr11 + 16756722 16756722 16756722 CCTGAAGTCAGGAGTTTGAGACCAGCCTGACCAACATGGAGAAACCCCATCTCTACTAAAAATAC CCTGAAGTCAGGAGTTTGAGACCAGCCTGACCGACATGGAGAAACCCCATCTCTACTAAAAATAC A G C11orf58 Ensembl:ENSG00000110696 Protein coding 3'UTR GSE38233;GSE107867 cultured B-cells;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 24183664,30559470 RNA-Seq:(High) rs1337116331 Functional Loss SNV dbSNP153 33..33 33 - - - 4601 RMVar_ID_4601 Human_SNP_ID_457293968 A-to-I Human chr11 + 16756801 16756801 16756801 GTGGTGGTGCATGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCCA GTGGTGGTGCATGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCCA A G C11orf58 Ensembl:ENSG00000110696 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1237868365 Functional Loss SNV dbSNP153 33..33 33 - - - 4602 RMVar_ID_4602 Human_SNP_ID_457293972 A-to-I Human chr11 + 16756836 16756836 16756836 AGGCTGAGGCAGGAGAATCACTTGAACCCAGGAAGCGGAGGTTGCAGTGAGCCAAGATCACCCCA AGGCTGAGGCAGGAGAATCACTTGAACCCAGGTAGCGGAGGTTGCAGTGAGCCAAGATCACCCCA A T C11orf58 Ensembl:ENSG00000110696 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1285556896 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1214070 4603 RMVar_ID_4603 Human_SNP_ID_457293982 A-to-I Human chr11 + 16756863 16756863 16756863 CCAGGAAGCGGAGGTTGCAGTGAGCCAAGATCACCCCATTGCACTCCAGCCTGGGCAACAAGAGC CCAGGAAGCGGAGGTTGCAGTGAGCCAAGATCGCCCCATTGCACTCCAGCCTGGGCAACAAGAGC A G C11orf58 Ensembl:ENSG00000110696 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1391100132 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1214070 4604 RMVar_ID_4604 Human_SNP_ID_457293999 A-to-I Human chr11 + 16756904 16756904 16756904 CACTCCAGCCTGGGCAACAAGAGCAAAACTCCATCTCAAAAAAAAAAAAAAAAAAAATTTAGAAT CACTCCAGCCTGGGCAACAAGAGCAAAACTCCGTCTCAAAAAAAAAAAAAAAAAAAATTTAGAAT A G C11orf58 Ensembl:ENSG00000110696 Protein coding 3'UTR GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1037632154 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1214070 4605 RMVar_ID_4605 Human_SNP_ID_457294019 A-to-I Human chr11 + 16756912 16756912 16756912 CCTGGGCAACAAGAGCAAAACTCCATCTCAAAAAAAAAAAAAAAAAAAATTTAGAATGTGTTAGA CCTGGGCAACAAGAGCAAAACTCCATCTCAAATAAAAAAAAAAAAAAAATTTAGAATGTGTTAGA A T C11orf58 Ensembl:ENSG00000110696 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1309327261 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1214070 4606 RMVar_ID_4606 Human_SNP_ID_457342852 A-to-I Human chr11 - 16954412 16954412 16954412 CTCCTGTCTCAACCTCCTGAGTAACTGAGACTATAGGTGTGCACTACCACACATGGCTAATTTAA CTCCTGTCTCAACCTCCTGAGTAACTGAGACTTTAGGTGTGCACTACCACACATGGCTAATTTAA T A PLEKHA7 Ensembl:ENSG00000166689 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs747173723 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 4607 RMVar_ID_4607 Human_SNP_ID_457342853 A-to-I Human chr11 - 16954412 16954412 16954412 CTCCTGTCTCAACCTCCTGAGTAACTGAGACTATAGGTGTGCACTACCACACATGGCTAATTTAA CTCCTGTCTCAACCTCCTGAGTAACTGAGACTGTAGGTGTGCACTACCACACATGGCTAATTTAA T C PLEKHA7 Ensembl:ENSG00000166689 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs747173723 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 4608 RMVar_ID_4608 Human_SNP_ID_457355488 A-to-I Human chr11 - 17007797 17007797 17007797 GGCCAAAGCAGGAGGATTGCTTGGGCTCAGGAATTTGAGACTAGCCTGGGCAACATGGTAAAACC GGCCAAAGCAGGAGGATTGCTTGGGCTCAGGATTTTGAGACTAGCCTGGGCAACATGGTAAAACC T A PLEKHA7 Ensembl:ENSG00000166689 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs752833297 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 4609 RMVar_ID_4609 Human_SNP_ID_457373875 A-to-I Human chr11 - 17076650 17076642 17076650 CCAGATACTTGGGATGCAGAGGTGAGAGGATCACCAGAGCCTAGAAGTCCCAGGCTGCAGTGAGC CCAGATACTTGGGATGCAGAGGTGAGAGGATC________CTAGAAGTCCCAGGCTGCAGTGAGC GGCTCTGGT G RPS13 Ensembl:ENSG00000110700 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1313832516 Functional Loss DEL dbSNP153 33..40 33 - - - Human_RBP_ID_11576558,Human_RBP_ID_18605734 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 4610 RMVar_ID_4610 Human_SNP_ID_457383585 A-to-I Human chr11 - 17112910 17112910 17112910 ATGTTGGTGCATGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGGATCACTTGAGCCCA ATGTTGGTGCATGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGGATCACTTGAGCCCA T C PIK3C2A Ensembl:ENSG00000011405 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs746550088 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126123,RMVar_hsa_circ_344936,RMVar_hsa_circ_148448,RMVar_hsa_circ_334889,RMVar_hsa_circ_8677,RMVar_hsa_circ_148451,RMVar_hsa_circ_42157,RMVar_hsa_circ_373124,RMVar_hsa_circ_309628,RMVar_hsa_circ_67722,RMVar_hsa_circ_148452,RMVar_hsa_circ_327626,RMVar_hsa_circ_346095,RMVar_hsa_circ_33768,RMVar_hsa_circ_377506,RMVar_hsa_circ_148458,RMVar_hsa_circ_9690,RMVar_hsa_circ_378889,RMVar_hsa_circ_322331,RMVar_hsa_circ_352620,RMVar_hsa_circ_314081,RMVar_hsa_circ_102808,RMVar_hsa_circ_47019,RMVar_hsa_circ_3293,RMVar_hsa_circ_148466,RMVar_hsa_circ_148461,RMVar_hsa_circ_148462,RMVar_hsa_circ_148463,RMVar_hsa_circ_374157,RMVar_hsa_circ_346776,RMVar_hsa_circ_366768,RMVar_hsa_circ_148464,RMVar_hsa_circ_368133,RMVar_hsa_circ_357487,RMVar_hsa_circ_109254,RMVar_hsa_circ_276157,RMVar_hsa_circ_79922,RMVar_hsa_circ_148468,RMVar_hsa_circ_8646,RMVar_hsa_circ_148467,RMVar_hsa_circ_148471,RMVar_hsa_circ_311180,RMVar_hsa_circ_342261,RMVar_hsa_circ_148465,RMVar_hsa_circ_352480,RMVar_hsa_circ_319696,RMVar_hsa_circ_6746,RMVar_hsa_circ_148473,RMVar_hsa_circ_148472,RMVar_hsa_circ_148477,RMVar_hsa_circ_313198,RMVar_hsa_circ_343789,RMVar_hsa_circ_314793,RMVar_hsa_circ_49961,RMVar_hsa_circ_297641,RMVar_hsa_circ_43619,RMVar_hsa_circ_148478,RMVar_hsa_circ_148475,RMVar_hsa_circ_148476,RMVar_hsa_circ_323508,RMVar_hsa_circ_356296,RMVar_hsa_circ_327494,RMVar_hsa_circ_312966,RMVar_hsa_circ_148480,RMVar_hsa_circ_148481,RMVar_hsa_circ_148482,RMVar_hsa_circ_148479 4611 RMVar_ID_4611 Human_SNP_ID_457386413 A-to-I Human chr11 - 17123389 17123389 17123389 CAAGAATTAGCTGAGCATGGTGCCACGTGCCTATAGTCCTAGCTACTTGGGAGGCTGCAATGGAA CAAGAATTAGCTGAGCATGGTGCCACGTGCCTGTAGTCCTAGCTACTTGGGAGGCTGCAATGGAA T C PIK3C2A Ensembl:ENSG00000011405 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1420601377 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11576839 RMVar_hsa_circ_126123,RMVar_hsa_circ_334889,RMVar_hsa_circ_148451,RMVar_hsa_circ_373124,RMVar_hsa_circ_67722,RMVar_hsa_circ_148452,RMVar_hsa_circ_33768,RMVar_hsa_circ_352620,RMVar_hsa_circ_102808,RMVar_hsa_circ_47019,RMVar_hsa_circ_3293,RMVar_hsa_circ_148463,RMVar_hsa_circ_374157,RMVar_hsa_circ_346776,RMVar_hsa_circ_148464,RMVar_hsa_circ_368133,RMVar_hsa_circ_357487,RMVar_hsa_circ_8646,RMVar_hsa_circ_352480,RMVar_hsa_circ_343789,RMVar_hsa_circ_49961,RMVar_hsa_circ_43619,RMVar_hsa_circ_148478,RMVar_hsa_circ_356296,RMVar_hsa_circ_97728,RMVar_hsa_circ_274714,RMVar_hsa_circ_343646,RMVar_hsa_circ_148479,RMVar_hsa_circ_148484,RMVar_hsa_circ_148485,RMVar_hsa_circ_331340,RMVar_hsa_circ_345201,RMVar_hsa_circ_3314,RMVar_hsa_circ_288952,RMVar_hsa_circ_364608,RMVar_hsa_circ_63623,RMVar_hsa_circ_112446,RMVar_hsa_circ_121538,RMVar_hsa_circ_148487,RMVar_hsa_circ_102170,RMVar_hsa_circ_29489,RMVar_hsa_circ_148490,RMVar_hsa_circ_148491,RMVar_hsa_circ_148492,RMVar_hsa_circ_148489,RMVar_hsa_circ_276713,RMVar_hsa_circ_31143,RMVar_hsa_circ_362080,RMVar_hsa_circ_271555,RMVar_hsa_circ_265765,RMVar_hsa_circ_148494,RMVar_hsa_circ_15456,RMVar_hsa_circ_373364,RMVar_hsa_circ_148493,RMVar_hsa_circ_268244,RMVar_hsa_circ_148495 4612 RMVar_ID_4612 Human_SNP_ID_457386931 A-to-I Human chr11 - 17125568 17125568 17125568 GGAGTTTTGCAGTGAGGCGAAATTGCACCACTACACTCCAGCCTGGGCGACAGAACGAGACTCCA GGAGTTTTGCAGTGAGGCGAAATTGCACCACTGCACTCCAGCCTGGGCGACAGAACGAGACTCCA T C PIK3C2A Ensembl:ENSG00000011405 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1565258832 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126123,RMVar_hsa_circ_334889,RMVar_hsa_circ_148451,RMVar_hsa_circ_373124,RMVar_hsa_circ_67722,RMVar_hsa_circ_148452,RMVar_hsa_circ_33768,RMVar_hsa_circ_352620,RMVar_hsa_circ_102808,RMVar_hsa_circ_47019,RMVar_hsa_circ_3293,RMVar_hsa_circ_148463,RMVar_hsa_circ_374157,RMVar_hsa_circ_346776,RMVar_hsa_circ_148464,RMVar_hsa_circ_368133,RMVar_hsa_circ_357487,RMVar_hsa_circ_8646,RMVar_hsa_circ_352480,RMVar_hsa_circ_343789,RMVar_hsa_circ_49961,RMVar_hsa_circ_43619,RMVar_hsa_circ_148478,RMVar_hsa_circ_356296,RMVar_hsa_circ_97728,RMVar_hsa_circ_274714,RMVar_hsa_circ_343646,RMVar_hsa_circ_148479,RMVar_hsa_circ_148484,RMVar_hsa_circ_148485,RMVar_hsa_circ_331340,RMVar_hsa_circ_345201,RMVar_hsa_circ_3314,RMVar_hsa_circ_288952,RMVar_hsa_circ_364608,RMVar_hsa_circ_63623,RMVar_hsa_circ_112446,RMVar_hsa_circ_121538,RMVar_hsa_circ_148487,RMVar_hsa_circ_102170,RMVar_hsa_circ_29489,RMVar_hsa_circ_148490,RMVar_hsa_circ_148491,RMVar_hsa_circ_148492,RMVar_hsa_circ_148489,RMVar_hsa_circ_276713,RMVar_hsa_circ_31143,RMVar_hsa_circ_362080,RMVar_hsa_circ_271555,RMVar_hsa_circ_265765,RMVar_hsa_circ_148494,RMVar_hsa_circ_15456,RMVar_hsa_circ_373364,RMVar_hsa_circ_148493,RMVar_hsa_circ_268244,RMVar_hsa_circ_148495 4613 RMVar_ID_4613 Human_SNP_ID_457386958 A-to-I Human chr11 - 17125655 17125655 17125655 AAAGTTATAGCCAGGTATGGTGGCTCGTGCCTATAGTCCCAGCTACTTGGGAGGCTGAGACGGGA AAAGTTATAGCCAGGTATGGTGGCTCGTGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGACGGGA T C PIK3C2A Ensembl:ENSG00000011405 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1023827598 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17559871 RMVar_hsa_circ_126123,RMVar_hsa_circ_334889,RMVar_hsa_circ_148451,RMVar_hsa_circ_373124,RMVar_hsa_circ_67722,RMVar_hsa_circ_148452,RMVar_hsa_circ_33768,RMVar_hsa_circ_352620,RMVar_hsa_circ_102808,RMVar_hsa_circ_47019,RMVar_hsa_circ_3293,RMVar_hsa_circ_148463,RMVar_hsa_circ_374157,RMVar_hsa_circ_346776,RMVar_hsa_circ_148464,RMVar_hsa_circ_368133,RMVar_hsa_circ_357487,RMVar_hsa_circ_8646,RMVar_hsa_circ_352480,RMVar_hsa_circ_343789,RMVar_hsa_circ_49961,RMVar_hsa_circ_43619,RMVar_hsa_circ_148478,RMVar_hsa_circ_356296,RMVar_hsa_circ_97728,RMVar_hsa_circ_274714,RMVar_hsa_circ_343646,RMVar_hsa_circ_148479,RMVar_hsa_circ_148484,RMVar_hsa_circ_148485,RMVar_hsa_circ_331340,RMVar_hsa_circ_345201,RMVar_hsa_circ_3314,RMVar_hsa_circ_288952,RMVar_hsa_circ_364608,RMVar_hsa_circ_63623,RMVar_hsa_circ_112446,RMVar_hsa_circ_121538,RMVar_hsa_circ_148487,RMVar_hsa_circ_102170,RMVar_hsa_circ_29489,RMVar_hsa_circ_148490,RMVar_hsa_circ_148491,RMVar_hsa_circ_148492,RMVar_hsa_circ_148489,RMVar_hsa_circ_276713,RMVar_hsa_circ_31143,RMVar_hsa_circ_362080,RMVar_hsa_circ_271555,RMVar_hsa_circ_265765,RMVar_hsa_circ_148494,RMVar_hsa_circ_15456,RMVar_hsa_circ_373364,RMVar_hsa_circ_148493,RMVar_hsa_circ_268244,RMVar_hsa_circ_148495 4614 RMVar_ID_4614 Human_SNP_ID_457387053 A-to-I Human chr11 - 17126002 17126002 17126002 CTCATGCCTCAGCCTCCAGAGTAGCTGAGATTACAGGTGTGTGCTACCATGCCTGGCTAATTTTT CTCATGCCTCAGCCTCCAGAGTAGCTGAGATTGCAGGTGTGTGCTACCATGCCTGGCTAATTTTT T C PIK3C2A Ensembl:ENSG00000011405 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1460349426 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126123,RMVar_hsa_circ_334889,RMVar_hsa_circ_148451,RMVar_hsa_circ_373124,RMVar_hsa_circ_67722,RMVar_hsa_circ_148452,RMVar_hsa_circ_33768,RMVar_hsa_circ_352620,RMVar_hsa_circ_102808,RMVar_hsa_circ_47019,RMVar_hsa_circ_3293,RMVar_hsa_circ_148463,RMVar_hsa_circ_374157,RMVar_hsa_circ_346776,RMVar_hsa_circ_148464,RMVar_hsa_circ_368133,RMVar_hsa_circ_357487,RMVar_hsa_circ_8646,RMVar_hsa_circ_352480,RMVar_hsa_circ_343789,RMVar_hsa_circ_49961,RMVar_hsa_circ_43619,RMVar_hsa_circ_148478,RMVar_hsa_circ_356296,RMVar_hsa_circ_97728,RMVar_hsa_circ_274714,RMVar_hsa_circ_343646,RMVar_hsa_circ_148479,RMVar_hsa_circ_148484,RMVar_hsa_circ_148485,RMVar_hsa_circ_331340,RMVar_hsa_circ_345201,RMVar_hsa_circ_3314,RMVar_hsa_circ_288952,RMVar_hsa_circ_364608,RMVar_hsa_circ_63623,RMVar_hsa_circ_112446,RMVar_hsa_circ_121538,RMVar_hsa_circ_148487,RMVar_hsa_circ_102170,RMVar_hsa_circ_29489,RMVar_hsa_circ_148490,RMVar_hsa_circ_148491,RMVar_hsa_circ_148492,RMVar_hsa_circ_148489,RMVar_hsa_circ_276713,RMVar_hsa_circ_31143,RMVar_hsa_circ_362080,RMVar_hsa_circ_271555,RMVar_hsa_circ_265765,RMVar_hsa_circ_148494,RMVar_hsa_circ_15456,RMVar_hsa_circ_373364,RMVar_hsa_circ_148493,RMVar_hsa_circ_268244,RMVar_hsa_circ_148495 4615 RMVar_ID_4615 Human_SNP_ID_457387949 A-to-I Human chr11 - 17129659 17129659 17129659 TGAACCCAGGAGGCGGAGGTTGCAGTGAGCCAAGATCGTGCCATTGCACTCCAGCCTAGGCAACA TGAACCCAGGAGGCGGAGGTTGCAGTGAGCCAGGATCGTGCCATTGCACTCCAGCCTAGGCAACA T C PIK3C2A Ensembl:ENSG00000011405 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs144091333 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126123,RMVar_hsa_circ_334889,RMVar_hsa_circ_148451,RMVar_hsa_circ_373124,RMVar_hsa_circ_148452,RMVar_hsa_circ_352620,RMVar_hsa_circ_102808,RMVar_hsa_circ_3293,RMVar_hsa_circ_148463,RMVar_hsa_circ_374157,RMVar_hsa_circ_148464,RMVar_hsa_circ_368133,RMVar_hsa_circ_8646,RMVar_hsa_circ_49961,RMVar_hsa_circ_43619,RMVar_hsa_circ_148478,RMVar_hsa_circ_97728,RMVar_hsa_circ_343646,RMVar_hsa_circ_148479,RMVar_hsa_circ_148485,RMVar_hsa_circ_331340,RMVar_hsa_circ_3314,RMVar_hsa_circ_288952,RMVar_hsa_circ_364608,RMVar_hsa_circ_112446,RMVar_hsa_circ_121538,RMVar_hsa_circ_148487,RMVar_hsa_circ_102170,RMVar_hsa_circ_29489,RMVar_hsa_circ_148490,RMVar_hsa_circ_148491,RMVar_hsa_circ_148492,RMVar_hsa_circ_148489,RMVar_hsa_circ_276713,RMVar_hsa_circ_31143,RMVar_hsa_circ_271555,RMVar_hsa_circ_94060,RMVar_hsa_circ_265765,RMVar_hsa_circ_148494,RMVar_hsa_circ_15456,RMVar_hsa_circ_373364,RMVar_hsa_circ_148493,RMVar_hsa_circ_268244,RMVar_hsa_circ_322379,RMVar_hsa_circ_148495,RMVar_hsa_circ_367708,RMVar_hsa_circ_291768,RMVar_hsa_circ_148496,RMVar_hsa_circ_11855,RMVar_hsa_circ_40399,RMVar_hsa_circ_148497,RMVar_hsa_circ_148498 4616 RMVar_ID_4616 Human_SNP_ID_457387958 A-to-I Human chr11 - 17129694 17129694 17129694 CCAGCTACTTGAGAGTCGGAGGCAGGAGAATCACTTGAACCCAGGAGGCGGAGGTTGCAGTGAGC CCAGCTACTTGAGAGTCGGAGGCAGGAGAATCCCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGC T G PIK3C2A Ensembl:ENSG00000011405 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1477480708 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11576947 RMVar_hsa_circ_126123,RMVar_hsa_circ_334889,RMVar_hsa_circ_148451,RMVar_hsa_circ_373124,RMVar_hsa_circ_148452,RMVar_hsa_circ_352620,RMVar_hsa_circ_102808,RMVar_hsa_circ_3293,RMVar_hsa_circ_148463,RMVar_hsa_circ_374157,RMVar_hsa_circ_148464,RMVar_hsa_circ_368133,RMVar_hsa_circ_8646,RMVar_hsa_circ_49961,RMVar_hsa_circ_43619,RMVar_hsa_circ_148478,RMVar_hsa_circ_97728,RMVar_hsa_circ_343646,RMVar_hsa_circ_148479,RMVar_hsa_circ_148485,RMVar_hsa_circ_331340,RMVar_hsa_circ_3314,RMVar_hsa_circ_288952,RMVar_hsa_circ_364608,RMVar_hsa_circ_112446,RMVar_hsa_circ_121538,RMVar_hsa_circ_148487,RMVar_hsa_circ_102170,RMVar_hsa_circ_29489,RMVar_hsa_circ_148490,RMVar_hsa_circ_148491,RMVar_hsa_circ_148492,RMVar_hsa_circ_148489,RMVar_hsa_circ_276713,RMVar_hsa_circ_31143,RMVar_hsa_circ_271555,RMVar_hsa_circ_94060,RMVar_hsa_circ_265765,RMVar_hsa_circ_148494,RMVar_hsa_circ_15456,RMVar_hsa_circ_373364,RMVar_hsa_circ_148493,RMVar_hsa_circ_268244,RMVar_hsa_circ_322379,RMVar_hsa_circ_148495,RMVar_hsa_circ_367708,RMVar_hsa_circ_291768,RMVar_hsa_circ_148496,RMVar_hsa_circ_11855,RMVar_hsa_circ_40399,RMVar_hsa_circ_148497,RMVar_hsa_circ_148498 4617 RMVar_ID_4617 Human_SNP_ID_457388304 A-to-I Human chr11 - 17131105 17131105 17131105 CAGCTCACTGCAAGCTCCACCTCTCGAGTTCAAGCAATTCTCCTGTCTCAGCCTCCTGAGTAACT CAGCTCACTGCAAGCTCCACCTCTCGAGTTCAGGCAATTCTCCTGTCTCAGCCTCCTGAGTAACT T C PIK3C2A Ensembl:ENSG00000011405 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs757165689 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126123,RMVar_hsa_circ_334889,RMVar_hsa_circ_148451,RMVar_hsa_circ_373124,RMVar_hsa_circ_148452,RMVar_hsa_circ_352620,RMVar_hsa_circ_102808,RMVar_hsa_circ_3293,RMVar_hsa_circ_148463,RMVar_hsa_circ_374157,RMVar_hsa_circ_148464,RMVar_hsa_circ_368133,RMVar_hsa_circ_8646,RMVar_hsa_circ_49961,RMVar_hsa_circ_43619,RMVar_hsa_circ_148478,RMVar_hsa_circ_97728,RMVar_hsa_circ_343646,RMVar_hsa_circ_148479,RMVar_hsa_circ_148485,RMVar_hsa_circ_331340,RMVar_hsa_circ_3314,RMVar_hsa_circ_288952,RMVar_hsa_circ_364608,RMVar_hsa_circ_112446,RMVar_hsa_circ_121538,RMVar_hsa_circ_148487,RMVar_hsa_circ_102170,RMVar_hsa_circ_29489,RMVar_hsa_circ_148490,RMVar_hsa_circ_148491,RMVar_hsa_circ_148492,RMVar_hsa_circ_148489,RMVar_hsa_circ_276713,RMVar_hsa_circ_31143,RMVar_hsa_circ_271555,RMVar_hsa_circ_94060,RMVar_hsa_circ_265765,RMVar_hsa_circ_148494,RMVar_hsa_circ_15456,RMVar_hsa_circ_373364,RMVar_hsa_circ_148493,RMVar_hsa_circ_268244,RMVar_hsa_circ_322379,RMVar_hsa_circ_148495,RMVar_hsa_circ_367708,RMVar_hsa_circ_291768,RMVar_hsa_circ_148496,RMVar_hsa_circ_11855,RMVar_hsa_circ_40399,RMVar_hsa_circ_148497,RMVar_hsa_circ_148498 4618 RMVar_ID_4618 Human_SNP_ID_457388416 A-to-I Human chr11 - 17131507 17131507 17131507 TGAGGCAGGAGAATGTCATGAATCCGGGAGGCAGAGCTTTCAGTGAGCTGAGATTGAGCCACCGC TGAGGCAGGAGAATGTCATGAATCCGGGAGGCGGAGCTTTCAGTGAGCTGAGATTGAGCCACCGC T C PIK3C2A Ensembl:ENSG00000011405 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1257365714 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_108326 RMVar_hsa_circ_126123,RMVar_hsa_circ_334889,RMVar_hsa_circ_148451,RMVar_hsa_circ_373124,RMVar_hsa_circ_148452,RMVar_hsa_circ_352620,RMVar_hsa_circ_102808,RMVar_hsa_circ_3293,RMVar_hsa_circ_148463,RMVar_hsa_circ_374157,RMVar_hsa_circ_148464,RMVar_hsa_circ_368133,RMVar_hsa_circ_8646,RMVar_hsa_circ_49961,RMVar_hsa_circ_43619,RMVar_hsa_circ_148478,RMVar_hsa_circ_97728,RMVar_hsa_circ_343646,RMVar_hsa_circ_148479,RMVar_hsa_circ_148485,RMVar_hsa_circ_331340,RMVar_hsa_circ_3314,RMVar_hsa_circ_288952,RMVar_hsa_circ_364608,RMVar_hsa_circ_112446,RMVar_hsa_circ_121538,RMVar_hsa_circ_148487,RMVar_hsa_circ_102170,RMVar_hsa_circ_29489,RMVar_hsa_circ_148490,RMVar_hsa_circ_148491,RMVar_hsa_circ_148492,RMVar_hsa_circ_148489,RMVar_hsa_circ_276713,RMVar_hsa_circ_31143,RMVar_hsa_circ_271555,RMVar_hsa_circ_94060,RMVar_hsa_circ_265765,RMVar_hsa_circ_148494,RMVar_hsa_circ_15456,RMVar_hsa_circ_373364,RMVar_hsa_circ_148493,RMVar_hsa_circ_268244,RMVar_hsa_circ_322379,RMVar_hsa_circ_148495,RMVar_hsa_circ_367708,RMVar_hsa_circ_291768,RMVar_hsa_circ_148496,RMVar_hsa_circ_11855,RMVar_hsa_circ_40399,RMVar_hsa_circ_148497,RMVar_hsa_circ_148498 4619 RMVar_ID_4619 Human_SNP_ID_457400049 A-to-I Human chr11 - 17179313 17179313 17179313 TATAAAAAATTTAAAAATTAGTTGGATGTAGTAGTACATGCCTGTAGTCCCAGCTGCTCAAGAGT TATAAAAAATTTAAAAATTAGTTGGATGTAGTGGTACATGCCTGTAGTCCCAGCTGCTCAAGAGT T C PIK3C2A Ensembl:ENSG00000011405 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs772287793 Functional Loss SNV dbSNP153 33..33 33 - - - 4620 RMVar_ID_4620 Human_SNP_ID_457411716 A-to-I Human chr11 + 17224671 17224671 17224671 TTTTGTATTTTTATTAGAGATGGGGTTTCTCCATGTTGGTTAGGCTGGTCCCGAACTCCCGACCT TTTTGTATTTTTATTAGAGATGGGGTTTCTCCTTGTTGGTTAGGCTGGTCCCGAACTCCCGACCT A T NUCB2 Ensembl:ENSG00000070081 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1018467602 Functional Loss SNV dbSNP153 33..33 33 - - - 4621 RMVar_ID_4621 Human_SNP_ID_457430272 A-to-I Human chr11 + 17298523 17298521 17298523 CCAGGAGTTTGAGGTTGCAGTGAGCCATGATTATATGACTGTACTCTAGCCCGCATGACACAGAG CCAGGAGTTTGAGGTTGCAGTGAGCCATGAT__TATGACTGTACTCTAGCCCGCATGACACAGAG TTA T NUCB2 Ensembl:ENSG00000070081 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1345701660 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_59257,RMVar_hsa_circ_73906,RMVar_hsa_circ_27238,RMVar_hsa_circ_148510,RMVar_hsa_circ_266913,RMVar_hsa_circ_294814,RMVar_hsa_circ_321174,RMVar_hsa_circ_324146,RMVar_hsa_circ_294969,RMVar_hsa_circ_148511,RMVar_hsa_circ_148509,RMVar_hsa_circ_352879 4622 RMVar_ID_4622 Human_SNP_ID_457430273 A-to-I Human chr11 + 17298523 17298523 17298523 CCAGGAGTTTGAGGTTGCAGTGAGCCATGATTATATGACTGTACTCTAGCCCGCATGACACAGAG CCAGGAGTTTGAGGTTGCAGTGAGCCATGATTGTATGACTGTACTCTAGCCCGCATGACACAGAG A G NUCB2 Ensembl:ENSG00000070081 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1373546071 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59257,RMVar_hsa_circ_73906,RMVar_hsa_circ_27238,RMVar_hsa_circ_148510,RMVar_hsa_circ_266913,RMVar_hsa_circ_294814,RMVar_hsa_circ_321174,RMVar_hsa_circ_324146,RMVar_hsa_circ_294969,RMVar_hsa_circ_148511,RMVar_hsa_circ_148509,RMVar_hsa_circ_352879 4623 RMVar_ID_4623 Human_SNP_ID_457438660 A-to-I Human chr11 + 17336126 17336126 17336126 CACCACACCCAGCTAATTTTTTTATTTTTAGTAGAGTCAGGGTTTCACTATGTTGGCCAGGCTGG CACCACACCCAGCTAATTTTTTTATTTTTAGTGGAGTCAGGGTTTCACTATGTTGGCCAGGCTGG A G NUCB2 Ensembl:ENSG00000070081 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1224546798 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_148517 4624 RMVar_ID_4624 Human_SNP_ID_457438930 A-to-I Human chr11 + 17337044 17337044 17337044 CTCACTATAGTCTCGAACTTCTGGGCTCAAGCAATCCTCCTGTCTCAGCTTCCTGAATAGCTGGG CTCACTATAGTCTCGAACTTCTGGGCTCAAGCGATCCTCCTGTCTCAGCTTCCTGAATAGCTGGG A G NUCB2 Ensembl:ENSG00000070081 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1398931548 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_148517 4625 RMVar_ID_4625 Human_SNP_ID_457439056 A-to-I Human chr11 + 17337666 17337666 17337666 TTATTTATTTATTTATTTTTTATTTTTGATACAGAGTTTCACTCTCGTTGCCCAGGCTAGAGTGC TTATTTATTTATTTATTTTTTATTTTTGATACGGAGTTTCACTCTCGTTGCCCAGGCTAGAGTGC A G NUCB2 Ensembl:ENSG00000070081 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388375825 Functional Loss SNV dbSNP153 33..33 33 - - - 4626 RMVar_ID_4626 Human_SNP_ID_457443335 A-to-I Human chr11 + 17355317 17355317 17355317 TACTTGGGAGGCTGAGACAGGAGGATCACTTGAGCCCAGGAGGTGGAGGCTGCAGTGAGCAGTGA TACTTGGGAGGCTGAGACAGGAGGATCACTTGGGCCCAGGAGGTGGAGGCTGCAGTGAGCAGTGA A G NCR3LG1 Ensembl:ENSG00000188211 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1454118988 Functional Loss SNV dbSNP153 33..33 33 - - - 4627 RMVar_ID_4627 Human_SNP_ID_457443455 A-to-I Human chr11 + 17355829 17355825 17355829 TATTTATTTGTTTGTTTTTGAGACAGAGTCTCACTCTGTCACTCGGGCTAGAGTGCAATGGCATT TATTTATTTGTTTGTTTTTGAGACAGAGT____CTCTGTCACTCGGGCTAGAGTGCAATGGCATT TCTCA T NCR3LG1 Ensembl:ENSG00000188211 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs752934291 Functional Loss DEL dbSNP153 30..33 33 - - - 4628 RMVar_ID_4628 Human_SNP_ID_457443459 A-to-I Human chr11 + 17355862 17355862 17355862 CTCTGTCACTCGGGCTAGAGTGCAATGGCATTATCACGGCTGACTGCAGCCTTGAACTTCTGGGC CTCTGTCACTCGGGCTAGAGTGCAATGGCATTGTCACGGCTGACTGCAGCCTTGAACTTCTGGGC A G NCR3LG1 Ensembl:ENSG00000188211 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968289687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11577941 4629 RMVar_ID_4629 Human_SNP_ID_457443483 A-to-I Human chr11 + 17355937 17355937 17355937 CTCTCACCTCAGCCTCCCAAGTAGCTGGGACTACAAGTGCTAACCACCATGCTGGGCTAATTTAT CTCTCACCTCAGCCTCCCAAGTAGCTGGGACTGCAAGTGCTAACCACCATGCTGGGCTAATTTAT A G NCR3LG1 Ensembl:ENSG00000188211 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025031878 Functional Loss SNV dbSNP153 33..33 33 - - - 4630 RMVar_ID_4630 Human_SNP_ID_457574082 A-to-I Human chr11 - 17870271 17870270 17870271 AGCATAATCTCCCTGTATTAGTACATTTTCATACTGCTGTAAATAACTGCCCAAGACTGGATAAT AGCATAATCTCCCTGTATTAGTACATTTTCAT_CTGCTGTAAATAACTGCCCAAGACTGGATAAT GT G SERGEF Ensembl:ENSG00000129158 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559557943 Functional Loss DEL dbSNP153 33..33 33 - - - 4631 RMVar_ID_4631 Human_SNP_ID_457622870 A-to-I Human chr11 - 18087202 18087202 18087202 CCTATTTAGTTCTGAAAATCCAGAATGGCTTGATGTTTACATGCACATTTTACAACTGCTTACTA CCTATTTAGTTCTGAAAATCCAGAATGGCTTGTTGTTTACATGCACATTTTACAACTGCTTACTA T A SAAL1 Ensembl:ENSG00000166788 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs962782801 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_393349,Human_RBP_ID_18605864,Human_RBP_ID_23497578,Human_RBP_ID_24912171 Human_Splice_Rec_1218086,Human_Splice_Rec_1218087,Human_Splice_Rec_1218106,Human_Splice_Rec_1218107,Human_Splice_Rec_1218120,Human_Splice_Rec_1218121,Human_Splice_Rec_1218132,Human_Splice_Rec_1218133,Human_Splice_Rec_1218150,Human_Splice_Rec_1218151,Human_Splice_Rec_1218182,Human_Splice_Rec_1218183,Human_Splice_Rec_1218191 Human_miRNA_ID_2335215,Human_miRNA_ID_2337449,Human_miRNA_ID_2339682,Human_miRNA_ID_2341917,Human_miRNA_ID_2344153 RMVar_hsa_circ_35791,RMVar_hsa_circ_96511,RMVar_hsa_circ_148541,RMVar_hsa_circ_81126,RMVar_hsa_circ_90588,RMVar_hsa_circ_148542,RMVar_hsa_circ_148543,RMVar_hsa_circ_119124,RMVar_hsa_circ_148545,RMVar_hsa_circ_302432,RMVar_hsa_circ_275289,RMVar_hsa_circ_306952,RMVar_hsa_circ_148544,RMVar_hsa_circ_75851,RMVar_hsa_circ_148547,RMVar_hsa_circ_148546 4632 RMVar_ID_4632 Human_SNP_ID_457682318 A-to-I Human chr11 - 18316129 18316129 18316129 TACCATGCCAGGCTAATTTTTAAAGTTTTTGTAGAGATGGGGTCTTGCTATGTTGCCCAGGCTGG TACCATGCCAGGCTAATTTTTAAAGTTTTTGTGGAGATGGGGTCTTGCTATGTTGCCCAGGCTGG T C HPS5 Ensembl:ENSG00000110756 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1217797887 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76873,RMVar_hsa_circ_148575,RMVar_hsa_circ_337241 4633 RMVar_ID_4633 Human_SNP_ID_457682350 A-to-I Human chr11 - 18316256 18316256 18316256 CAGGTTGTCTCTGTTGCTCAGGCCTAAGTGCAATGGGGAGATCCTAGCTCACTGTAACCTCAAAC CAGGTTGTCTCTGTTGCTCAGGCCTAAGTGCAGTGGGGAGATCCTAGCTCACTGTAACCTCAAAC T C HPS5 Ensembl:ENSG00000110756 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1301262320 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76873,RMVar_hsa_circ_148575,RMVar_hsa_circ_337241 4634 RMVar_ID_4634 Human_SNP_ID_457682616 A-to-I Human chr11 - 18317308 18317308 18317308 GAGGTTGCAGTGAGTCGAGGTCATGCCACTGCACTGTAGCCTGGGCAACAGAGTAAGACTCTCTC GAGGTTGCAGTGAGTCGAGGTCATGCCACTGCTCTGTAGCCTGGGCAACAGAGTAAGACTCTCTC T A HPS5 Ensembl:ENSG00000110756 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs948372114 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76873,RMVar_hsa_circ_148575,RMVar_hsa_circ_337241 4635 RMVar_ID_4635 Human_SNP_ID_457682651 A-to-I Human chr11 - 18317420 18317420 18317420 GAAACTTTGTCTCTACTAAAAATACAAAAATTAGCCGGGCAAGGTGGCACGCGCCTGTAATCCCA GAAACTTTGTCTCTACTAAAAATACAAAAATTGGCCGGGCAAGGTGGCACGCGCCTGTAATCCCA T C HPS5 Ensembl:ENSG00000110756 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1341852478 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76873,RMVar_hsa_circ_148575,RMVar_hsa_circ_337241 4636 RMVar_ID_4636 Human_SNP_ID_457685573 A-to-I Human chr11 + 18327730 18327730 18327730 CTCATTTCAGCCTCCCGACTTGCTGGGACTACAGATGTGTACCACCAGGCCCAGCTAATTTTTAT CTCATTTCAGCCTCCCGACTTGCTGGGACTACCGATGTGTACCACCAGGCCCAGCTAATTTTTAT A C GTF2H1 Ensembl:ENSG00000110768 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7936225 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75172 4637 RMVar_ID_4637 Human_SNP_ID_457685574 A-to-I Human chr11 + 18327730 18327730 18327730 CTCATTTCAGCCTCCCGACTTGCTGGGACTACAGATGTGTACCACCAGGCCCAGCTAATTTTTAT CTCATTTCAGCCTCCCGACTTGCTGGGACTACGGATGTGTACCACCAGGCCCAGCTAATTTTTAT A G GTF2H1 Ensembl:ENSG00000110768 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7936225 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75172 4638 RMVar_ID_4638 Human_SNP_ID_457685603 A-to-I Human chr11 + 18327823 18327823 18327823 GTTGCACGGGCTGGTCGCAAACTCCTGGTCTCAGGCAGTCTGTCCGCCTCGGCTTCCTAAAGTGA GTTGCACGGGCTGGTCGCAAACTCCTGGTCTCGGGCAGTCTGTCCGCCTCGGCTTCCTAAAGTGA A G GTF2H1 Ensembl:ENSG00000110768 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1233119659 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75172 4639 RMVar_ID_4639 Human_SNP_ID_457685604 A-to-I Human chr11 + 18327827 18327827 18327827 CACGGGCTGGTCGCAAACTCCTGGTCTCAGGCAGTCTGTCCGCCTCGGCTTCCTAAAGTGATGAG CACGGGCTGGTCGCAAACTCCTGGTCTCAGGCGGTCTGTCCGCCTCGGCTTCCTAAAGTGATGAG A G GTF2H1 Ensembl:ENSG00000110768 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1281159239 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75172 4640 RMVar_ID_4640 Human_SNP_ID_457685660 A-to-I Human chr11 + 18328046 18328046 18328046 TAACATGGTGAAACCCCATCTCTACTAAACATACAAAAATTAGCCAGCCATGGTGGCATGTGCCT TAACATGGTGAAACCCCATCTCTACTAAACATGCAAAAATTAGCCAGCCATGGTGGCATGTGCCT A G GTF2H1 Ensembl:ENSG00000110768 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1292032133 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75172 4641 RMVar_ID_4641 Human_SNP_ID_457685798 A-to-I Human chr11 + 18328468 18328468 18328468 CTGGGAGGAGGAGGTTGCAGTGAGCCAAGATCACGCCACTGCACTCCAGCCTGGGTGACAGAGCA CTGGGAGGAGGAGGTTGCAGTGAGCCAAGATCGCGCCACTGCACTCCAGCCTGGGTGACAGAGCA A G GTF2H1 Ensembl:ENSG00000110768 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1253610363 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75172 4642 RMVar_ID_4642 Human_SNP_ID_457686559 A-to-I Human chr11 + 18331112 18331112 18331112 CTTTCATCCCCAGGCTGGAGTACAATGTTGCGATCTCACCTCACTGCAGCCTCTGCCTCCTGGGC CTTTCATCCCCAGGCTGGAGTACAATGTTGCGGTCTCACCTCACTGCAGCCTCTGCCTCCTGGGC A G GTF2H1 Ensembl:ENSG00000110768 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs899727006 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19621450 RMVar_hsa_circ_75172 4643 RMVar_ID_4643 Human_SNP_ID_457688274 A-to-I Human chr11 + 18337227 18337227 18337227 GAGGTGGGTGGATCACTTGAAGTCAGAAGTTCAAGACCAACCCAGCCAACATGGTGAAACTCCAC GAGGTGGGTGGATCACTTGAAGTCAGAAGTTCGAGACCAACCCAGCCAACATGGTGAAACTCCAC A G GTF2H1 Ensembl:ENSG00000110768 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1424903542 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12993,RMVar_hsa_circ_297397,RMVar_hsa_circ_348743,RMVar_hsa_circ_116221,RMVar_hsa_circ_311867,RMVar_hsa_circ_148582,RMVar_hsa_circ_341215,RMVar_hsa_circ_368481,RMVar_hsa_circ_312626,RMVar_hsa_circ_148583,RMVar_hsa_circ_148584 4644 RMVar_ID_4644 Human_SNP_ID_457690096 A-to-I Human chr11 + 18343947 18343947 18343947 TCTTGACCTCTTGGGCTCAAGCAATCTGCCTTAGGCTCCTGAGTAGCTGGGACTGTAGCACAGGC TCTTGACCTCTTGGGCTCAAGCAATCTGCCTTGGGCTCCTGAGTAGCTGGGACTGTAGCACAGGC A G GTF2H1 Ensembl:ENSG00000110768 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1305736659 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11580717 RMVar_hsa_circ_22723,RMVar_hsa_circ_12993,RMVar_hsa_circ_116221,RMVar_hsa_circ_27045,RMVar_hsa_circ_148582,RMVar_hsa_circ_368481,RMVar_hsa_circ_44053,RMVar_hsa_circ_321904,RMVar_hsa_circ_376156,RMVar_hsa_circ_148585,RMVar_hsa_circ_358951,RMVar_hsa_circ_321678,RMVar_hsa_circ_148586,RMVar_hsa_circ_148587 4645 RMVar_ID_4645 Human_SNP_ID_457690121 A-to-I Human chr11 + 18344028 18344028 18344028 TTTTATTTTTTGTAGAGACAGGGTCTCCCTATATTTCCCAGGCTGGTCTGAACTCCTGGGCTCAA TTTTATTTTTTGTAGAGACAGGGTCTCCCTATGTTTCCCAGGCTGGTCTGAACTCCTGGGCTCAA A G GTF2H1 Ensembl:ENSG00000110768 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs542845614 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22723,RMVar_hsa_circ_12993,RMVar_hsa_circ_116221,RMVar_hsa_circ_27045,RMVar_hsa_circ_148582,RMVar_hsa_circ_368481,RMVar_hsa_circ_44053,RMVar_hsa_circ_321904,RMVar_hsa_circ_376156,RMVar_hsa_circ_148585,RMVar_hsa_circ_358951,RMVar_hsa_circ_321678,RMVar_hsa_circ_148586,RMVar_hsa_circ_148587 4646 RMVar_ID_4646 Human_SNP_ID_457691540 A-to-I Human chr11 + 18348902 18348901 18348903 TTTGTTGTTGTTATTGTTTGTTTTTTTGAGACAGAGTCTTGCTCTGTCACCCAGGCTGGAGTGCA TTTGTTGTTGTTATTGTTTGTTTTTTTGAGAC__AGTCTTGCTCTGTCACCCAGGCTGGAGTGCA CAG C GTF2H1 Ensembl:ENSG00000110768 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs774665126 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_3372297 RMVar_hsa_circ_22723,RMVar_hsa_circ_12993,RMVar_hsa_circ_116221,RMVar_hsa_circ_148582,RMVar_hsa_circ_44053,RMVar_hsa_circ_321904,RMVar_hsa_circ_376156,RMVar_hsa_circ_321678,RMVar_hsa_circ_148586,RMVar_hsa_circ_341439,RMVar_hsa_circ_148587,RMVar_hsa_circ_320307 4647 RMVar_ID_4647 Human_SNP_ID_457691576 A-to-I Human chr11 + 18349056 18349056 18349056 AGCTGGGATTACAGGCGTGCACCACCATACCTAGCTAATTTTTGTATTTTTAGTAGAGACGGAGT AGCTGGGATTACAGGCGTGCACCACCATACCTGGCTAATTTTTGTATTTTTAGTAGAGACGGAGT A G GTF2H1 Ensembl:ENSG00000110768 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1003879206 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22723,RMVar_hsa_circ_12993,RMVar_hsa_circ_116221,RMVar_hsa_circ_148582,RMVar_hsa_circ_44053,RMVar_hsa_circ_321904,RMVar_hsa_circ_376156,RMVar_hsa_circ_321678,RMVar_hsa_circ_148586,RMVar_hsa_circ_341439,RMVar_hsa_circ_148587,RMVar_hsa_circ_320307 4648 RMVar_ID_4648 Human_SNP_ID_457691580 A-to-I Human chr11 + 18349075 18349075 18349075 CACCACCATACCTAGCTAATTTTTGTATTTTTAGTAGAGACGGAGTTTTGCCATATTGGCCAGGC CACCACCATACCTAGCTAATTTTTGTATTTTTGGTAGAGACGGAGTTTTGCCATATTGGCCAGGC A G GTF2H1 Ensembl:ENSG00000110768 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1457798891 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11580760 RMVar_hsa_circ_22723,RMVar_hsa_circ_12993,RMVar_hsa_circ_116221,RMVar_hsa_circ_148582,RMVar_hsa_circ_44053,RMVar_hsa_circ_321904,RMVar_hsa_circ_376156,RMVar_hsa_circ_321678,RMVar_hsa_circ_148586,RMVar_hsa_circ_341439,RMVar_hsa_circ_148587,RMVar_hsa_circ_320307 4649 RMVar_ID_4649 Human_SNP_ID_457691694 A-to-I Human chr11 + 18349544 18349544 18349544 GTCTCTATTAAAAATACAGAAATTAGCCAGGCATGGTGACGTGCGCCTGTAATTCCAGCTACCTG GTCTCTATTAAAAATACAGAAATTAGCCAGGCGTGGTGACGTGCGCCTGTAATTCCAGCTACCTG A G GTF2H1 Ensembl:ENSG00000110768 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs528067605 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22723,RMVar_hsa_circ_12993,RMVar_hsa_circ_116221,RMVar_hsa_circ_148582,RMVar_hsa_circ_44053,RMVar_hsa_circ_321904,RMVar_hsa_circ_376156,RMVar_hsa_circ_321678,RMVar_hsa_circ_148586,RMVar_hsa_circ_341439,RMVar_hsa_circ_148587,RMVar_hsa_circ_320307 4650 RMVar_ID_4650 Human_SNP_ID_457693490 A-to-I Human chr11 + 18356159 18356159 18356159 TAGTCCCAGCACTTTGGGAGGCCGAGGCACGCAGATCACTTGAGAGCTCTAGACCACCCTGGCCA TAGTCCCAGCACTTTGGGAGGCCGAGGCACGCGGATCACTTGAGAGCTCTAGACCACCCTGGCCA A G GTF2H1 Ensembl:ENSG00000110768 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs866619755 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22723,RMVar_hsa_circ_116221,RMVar_hsa_circ_148582,RMVar_hsa_circ_44053,RMVar_hsa_circ_376156,RMVar_hsa_circ_148586,RMVar_hsa_circ_272950,RMVar_hsa_circ_320307,RMVar_hsa_circ_337574,RMVar_hsa_circ_148588 4651 RMVar_ID_4651 Human_SNP_ID_457694838 A-to-I Human chr11 + 18361002 18361002 18361002 TAATTTTTGTATTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTCGACC TAATTTTTGTATTTTAGTAGAGACGGGGTTTCCCCATGTTGGCCAGGCTGGTCTCAAACTCGACC A C GTF2H1 Ensembl:ENSG00000110768 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs895741819 Functional Loss SNV dbSNP153 33..33 33 - - - 4652 RMVar_ID_4652 Human_SNP_ID_457694951 A-to-I Human chr11 + 18361426 18361426 18361426 CGGTGGCTCATGCCTGTAATCCCAGCACATTGAGAGGCCAAGGCAGGCTGATCACTTGAGGTCAG CGGTGGCTCATGCCTGTAATCCCAGCACATTGGGAGGCCAAGGCAGGCTGATCACTTGAGGTCAG A G GTF2H1 Ensembl:ENSG00000110768 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs972916542 Functional Loss SNV dbSNP153 33..33 33 - - - 4653 RMVar_ID_4653 Human_SNP_ID_457694984 A-to-I Human chr11 + 18361548 18361548 18361548 AAAATTAGCCTGGCATGGTGGCGCATGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGACAGGAGA AAAATTAGCCTGGCATGGTGGCGCATGCCTGTGGTCCCAGCTACTCGGGAGGCTGAGACAGGAGA A G GTF2H1 Ensembl:ENSG00000110768 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1480994213 Functional Loss SNV dbSNP153 33..33 33 - - - 4654 RMVar_ID_4654 Human_SNP_ID_457694987 A-to-I Human chr11 + 18361558 18361558 18361558 TGGCATGGTGGCGCATGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGACAGGAGAATTGCTTGAA TGGCATGGTGGCGCATGCCTGTAGTCCCAGCTGCTCGGGAGGCTGAGACAGGAGAATTGCTTGAA A G GTF2H1 Ensembl:ENSG00000110768 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1482626717 Functional Loss SNV dbSNP153 33..33 33 - - - 4655 RMVar_ID_4655 Human_SNP_ID_457694995 A-to-I Human chr11 + 18361573 18361573 18361573 TGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGACAGGAGAATTGCTTGAACCTGGGAGACAGGGG TGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCTTGAACCTGGGAGACAGGGG A G GTF2H1 Ensembl:ENSG00000110768 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1484898743 Functional Loss SNV dbSNP153 33..33 33 - - - 4656 RMVar_ID_4656 Human_SNP_ID_457695609 A-to-I Human chr11 + 18363811 18363811 18363811 AAGGATGCTGAGGGCCAGGCGCGGTGGCTTACACCTGTAATCCCAGTACTTTGGGAGGCTGAGGC AAGGATGCTGAGGGCCAGGCGCGGTGGCTTACGCCTGTAATCCCAGTACTTTGGGAGGCTGAGGC A G GTF2H1 Ensembl:ENSG00000110768 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs567660131 Functional Loss SNV dbSNP153 33..33 33 - - - 4657 RMVar_ID_4657 Human_SNP_ID_457696629 A-to-I Human chr11 + 18367805 18367805 18367805 ATGAGCCCAGGAGATTGAGGCTGCAATGAGCTATGATCACACCACTGCACTACAGCCTGGACAGT ATGAGCCCAGGAGATTGAGGCTGCAATGAGCTGTGATCACACCACTGCACTACAGCCTGGACAGT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910201054 Functional Loss SNV dbSNP153 33..33 33 - - - 4658 RMVar_ID_4658 Human_SNP_ID_457698101 A-to-I Human chr11 + 18372678 18372678 18372678 TAGAGACAAGTTCTTGCCATGTTGCCCAGACTAGTCTTGGACTCCTGGGCTCAAGCAATCTGCGT TAGAGACAAGTTCTTGCCATGTTGCCCAGACTGGTCTTGGACTCCTGGGCTCAAGCAATCTGCGT A G lnc-GTF2H1-1 RNACentral:URS00008BA165 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1362830567 Functional Loss SNV dbSNP153 33..33 33 - - - 4659 RMVar_ID_4659 Human_SNP_ID_457705080 A-to-I Human chr11 + 18398718 18398718 18398718 TCACTGCTAGCTCTGCCTCCCGGGTTCATACCATTCTCCTGTCTCAGCCTCCCAAGTAGCTGGGA TCACTGCTAGCTCTGCCTCCCGGGTTCATACCGTTCTCCTGTCTCAGCCTCCCAAGTAGCTGGGA A G LDHA Ensembl:ENSG00000134333 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1307831133 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91084,RMVar_hsa_circ_114054,RMVar_hsa_circ_148591,RMVar_hsa_circ_148592,RMVar_hsa_circ_148593,RMVar_hsa_circ_108242 4660 RMVar_ID_4660 Human_SNP_ID_457705082 A-to-I Human chr11 + 18398731 18398731 18398731 TGCCTCCCGGGTTCATACCATTCTCCTGTCTCAGCCTCCCAAGTAGCTGGGACTACAGGCACCCA TGCCTCCCGGGTTCATACCATTCTCCTGTCTCGGCCTCCCAAGTAGCTGGGACTACAGGCACCCA A G LDHA Ensembl:ENSG00000134333 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1394628404 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91084,RMVar_hsa_circ_114054,RMVar_hsa_circ_148591,RMVar_hsa_circ_148592,RMVar_hsa_circ_148593,RMVar_hsa_circ_108242 4661 RMVar_ID_4661 Human_SNP_ID_457705087 A-to-I Human chr11 + 18398753 18398753 18398753 CTCCTGTCTCAGCCTCCCAAGTAGCTGGGACTACAGGCACCCACCACCACGCCTGGCTAAATGTT CTCCTGTCTCAGCCTCCCAAGTAGCTGGGACTGCAGGCACCCACCACCACGCCTGGCTAAATGTT A G LDHA Ensembl:ENSG00000134333 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7117399 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91084,RMVar_hsa_circ_114054,RMVar_hsa_circ_148591,RMVar_hsa_circ_148592,RMVar_hsa_circ_148593,RMVar_hsa_circ_108242 4662 RMVar_ID_4662 Human_SNP_ID_457706723 A-to-I Human chr11 + 18404048 18404048 18404048 TGCCTCCCGGGTTCAGGCGATTCTCCTGCCTCAGCCTCCTGGGTACCTGGGACTACAGGCATATG TGCCTCCCGGGTTCAGGCGATTCTCCTGCCTCCGCCTCCTGGGTACCTGGGACTACAGGCATATG A C LDHA Ensembl:ENSG00000134333 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1333561251 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37723,RMVar_hsa_circ_106856,RMVar_hsa_circ_304781,RMVar_hsa_circ_148596,RMVar_hsa_circ_322635 4663 RMVar_ID_4663 Human_SNP_ID_457707187 A-to-I Human chr11 + 18405770 18405770 18405770 TAATGTCCATTAGGCCTGTTCAACACATAGATACTTGATAATTTGACTACAAAAAAGTCTTGTTC TAATGTCCATTAGGCCTGTTCAACACATAGATGCTTGATAATTTGACTACAAAAAAGTCTTGTTC A G AC084117.1,LDHA Ensembl:ENSG00000256006,Ensembl:ENSG00000134333 lincRNA,Protein coding exon,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs3781641 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5553425 Human_Splice_Rec_1218935 Human_miRNA_ID_3150586,Human_miRNA_ID_3166240,Human_miRNA_ID_3166337,Human_miRNA_ID_3186993 RMVar_hsa_circ_106856,RMVar_hsa_circ_148596 4664 RMVar_ID_4664 Human_SNP_ID_457707188 A-to-I Human chr11 + 18405770 18405770 18405770 TAATGTCCATTAGGCCTGTTCAACACATAGATACTTGATAATTTGACTACAAAAAAGTCTTGTTC TAATGTCCATTAGGCCTGTTCAACACATAGATTCTTGATAATTTGACTACAAAAAAGTCTTGTTC A T AC084117.1,LDHA Ensembl:ENSG00000256006,Ensembl:ENSG00000134333 lincRNA,Protein coding exon,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs3781641 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5553425 Human_Splice_Rec_1218935 Human_miRNA_ID_3150586,Human_miRNA_ID_3166240,Human_miRNA_ID_3166337,Human_miRNA_ID_3186993 RMVar_hsa_circ_106856,RMVar_hsa_circ_148596 4665 RMVar_ID_4665 Human_SNP_ID_457707395 A-to-I Human chr11 + 18406515 18406515 18406515 CCAAGGGGTGGATCACCTGAGGTCAGTAGTTCAAGACCAGCCTGACCAACATGGTGAAACCCTGT CCAAGGGGTGGATCACCTGAGGTCAGTAGTTCGAGACCAGCCTGACCAACATGGTGAAACCCTGT A G AC084117.1,LDHA Ensembl:ENSG00000256006,Ensembl:ENSG00000134333 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1415476514 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106856,RMVar_hsa_circ_148596 4666 RMVar_ID_4666 Human_SNP_ID_457707414 A-to-I Human chr11 + 18406595 18406595 18406595 AGAATTAGCCAGGTGTGGTGGCAGGCGCCTGTAATCCCAGCTACTTGGGAGACTGAGGCAGAAGA AGAATTAGCCAGGTGTGGTGGCAGGCGCCTGTGATCCCAGCTACTTGGGAGACTGAGGCAGAAGA A G AC084117.1,LDHA Ensembl:ENSG00000256006,Ensembl:ENSG00000134333 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1024433212 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106856,RMVar_hsa_circ_148596 4667 RMVar_ID_4667 Human_SNP_ID_457707448 A-to-I Human chr11 + 18406717 18406717 18406717 CAGCCTGGGCAACAAGAGTGAAACTCCATCTCAAAAGAAAAAAAAAAGCGGCTGGGCTCTGTGGC CAGCCTGGGCAACAAGAGTGAAACTCCATCTCGAAAGAAAAAAAAAAGCGGCTGGGCTCTGTGGC A G AC084117.1,LDHA Ensembl:ENSG00000256006,Ensembl:ENSG00000134333 lincRNA,Protein coding exon,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10832933 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6111796 Human_Splice_Rec_1218936 RMVar_hsa_circ_106856,RMVar_hsa_circ_148596 4668 RMVar_ID_4668 Human_SNP_ID_457707449 A-to-I Human chr11 + 18406717 18406717 18406717 CAGCCTGGGCAACAAGAGTGAAACTCCATCTCAAAAGAAAAAAAAAAGCGGCTGGGCTCTGTGGC CAGCCTGGGCAACAAGAGTGAAACTCCATCTCTAAAGAAAAAAAAAAGCGGCTGGGCTCTGTGGC A T AC084117.1,LDHA Ensembl:ENSG00000256006,Ensembl:ENSG00000134333 lincRNA,Protein coding exon,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10832933 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6111796 Human_Splice_Rec_1218936 RMVar_hsa_circ_106856,RMVar_hsa_circ_148596 4669 RMVar_ID_4669 Human_SNP_ID_457729662 A-to-I Human chr11 - 18490366 18490366 18490366 GCCTGGCAAAAACAGTATTTGATGAAGCAATTACTGAATTGGATACACTGAATGAAGAGTCTTAT GCCTGGCAAAAACAGTATTTGATGAAGCAATTGCTGAATTGGATACACTGAATGAAGAGTCTTAT T C YWHABP2,TSG101 Ensembl:ENSG00000256464,Ensembl:ENSG00000074319 Pseudogene,Protein coding exon,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1375041229 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17351183 RMVar_hsa_circ_91752,RMVar_hsa_circ_118680,RMVar_hsa_circ_125499,RMVar_hsa_circ_148601,RMVar_hsa_circ_148605,RMVar_hsa_circ_148600,RMVar_hsa_circ_148604,RMVar_hsa_circ_148606,RMVar_hsa_circ_29879 4670 RMVar_ID_4670 Human_SNP_ID_457729671 A-to-I Human chr11 - 18490399 18490399 18490399 ATGAGATTCTAAACTCTACTGAAAAGGCCTGCAGCCTGGCAAAAACAGTATTTGATGAAGCAATT ATGAGATTCTAAACTCTACTGAAAAGGCCTGCTGCCTGGCAAAAACAGTATTTGATGAAGCAATT T A YWHABP2,TSG101 Ensembl:ENSG00000256464,Ensembl:ENSG00000074319 Pseudogene,Protein coding exon,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1459889887 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91752,RMVar_hsa_circ_118680,RMVar_hsa_circ_125499,RMVar_hsa_circ_148601,RMVar_hsa_circ_148605,RMVar_hsa_circ_148600,RMVar_hsa_circ_148604,RMVar_hsa_circ_148606,RMVar_hsa_circ_29879 4671 RMVar_ID_4671 Human_SNP_ID_457733284 A-to-I Human chr11 - 18504021 18504021 18504021 AATTTTTCTATTTTTGTAGAAATGGTTTCGCCATGTTGTCTAGGCTTGCCTTGAACTCCTGGACT AATTTTTCTATTTTTGTAGAAATGGTTTCGCCGTGTTGTCTAGGCTTGCCTTGAACTCCTGGACT T C TSG101 Ensembl:ENSG00000074319 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904214521 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_148608,RMVar_hsa_circ_91752,RMVar_hsa_circ_118680,RMVar_hsa_circ_148605,RMVar_hsa_circ_148600,RMVar_hsa_circ_148606,RMVar_hsa_circ_127586,RMVar_hsa_circ_310762,RMVar_hsa_circ_349090,RMVar_hsa_circ_287965,RMVar_hsa_circ_148609,RMVar_hsa_circ_148607 4672 RMVar_ID_4672 Human_SNP_ID_457733920 A-to-I Human chr11 - 18506568 18506568 18506568 CTCCTGCCTCAGCCTCCCTAGCAGTTGGGACTACAGGCTGTGCCACCATTCCCGGCTAATTTTTG CTCCTGCCTCAGCCTCCCTAGCAGTTGGGACTGCAGGCTGTGCCACCATTCCCGGCTAATTTTTG T C TSG101 Ensembl:ENSG00000074319 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1476113394 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6061378 RMVar_hsa_circ_148608,RMVar_hsa_circ_91752,RMVar_hsa_circ_118680,RMVar_hsa_circ_148605,RMVar_hsa_circ_148600,RMVar_hsa_circ_148606,RMVar_hsa_circ_127586,RMVar_hsa_circ_310762,RMVar_hsa_circ_349090,RMVar_hsa_circ_287965,RMVar_hsa_circ_148609,RMVar_hsa_circ_148607 4673 RMVar_ID_4673 Human_SNP_ID_457735385 A-to-I Human chr11 - 18512242 18512242 18512242 ACCACCACACCTGGCTAATTTTTGTATTTTTTAGTAGAGATGGGGTTTTGCTACATTGGCCAGTC ACCACCACACCTGGCTAATTTTTGTATTTTTTGGTAGAGATGGGGTTTTGCTACATTGGCCAGTC T C TSG101 Ensembl:ENSG00000074319 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs937173046 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_148608,RMVar_hsa_circ_91752,RMVar_hsa_circ_118680,RMVar_hsa_circ_148605,RMVar_hsa_circ_148600,RMVar_hsa_circ_148606,RMVar_hsa_circ_310762,RMVar_hsa_circ_349090,RMVar_hsa_circ_148609,RMVar_hsa_circ_148611,RMVar_hsa_circ_319373,RMVar_hsa_circ_332052,RMVar_hsa_circ_287309 4674 RMVar_ID_4674 Human_SNP_ID_457735679 A-to-I Human chr11 - 18513372 18513372 18513372 AGGATCACTTGAGCCTGGGAATTCGAGGCTGCAGTGAGCCATGATTGCATCACTGTCCTCCAGCC AGGATCACTTGAGCCTGGGAATTCGAGGCTGCGGTGAGCCATGATTGCATCACTGTCCTCCAGCC T C TSG101 Ensembl:ENSG00000074319 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1337170572 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_148608,RMVar_hsa_circ_91752,RMVar_hsa_circ_118680,RMVar_hsa_circ_148605,RMVar_hsa_circ_148600,RMVar_hsa_circ_148606,RMVar_hsa_circ_310762,RMVar_hsa_circ_349090,RMVar_hsa_circ_148609,RMVar_hsa_circ_148611,RMVar_hsa_circ_319373,RMVar_hsa_circ_332052,RMVar_hsa_circ_287309 4675 RMVar_ID_4675 Human_SNP_ID_457735686 A-to-I Human chr11 - 18513398 18513398 18513398 CCAGCTACTCAGGAGGCTAAGGTGAAAGGATCACTTGAGCCTGGGAATTCGAGGCTGCAGTGAGC CCAGCTACTCAGGAGGCTAAGGTGAAAGGATCCCTTGAGCCTGGGAATTCGAGGCTGCAGTGAGC T G TSG101 Ensembl:ENSG00000074319 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1380326391 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_148608,RMVar_hsa_circ_91752,RMVar_hsa_circ_118680,RMVar_hsa_circ_148605,RMVar_hsa_circ_148600,RMVar_hsa_circ_148606,RMVar_hsa_circ_310762,RMVar_hsa_circ_349090,RMVar_hsa_circ_148609,RMVar_hsa_circ_148611,RMVar_hsa_circ_319373,RMVar_hsa_circ_332052,RMVar_hsa_circ_287309 4676 RMVar_ID_4676 Human_SNP_ID_457737647 A-to-I Human chr11 - 18521466 18521466 18521466 TACTTGGGAGGCGGTGGTGGGAGTATCACTTGAGTCCAGGAGGTTGAGGCTGAAGTGAGCCATGA TACTTGGGAGGCGGTGGTGGGAGTATCACTTGGGTCCAGGAGGTTGAGGCTGAAGTGAGCCATGA T C TSG101 Ensembl:ENSG00000074319 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs962490902 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91752,RMVar_hsa_circ_148606 4677 RMVar_ID_4677 Human_SNP_ID_457737650 A-to-I Human chr11 - 18521471 18521471 18521471 CCAGCTACTTGGGAGGCGGTGGTGGGAGTATCACTTGAGTCCAGGAGGTTGAGGCTGAAGTGAGC CCAGCTACTTGGGAGGCGGTGGTGGGAGTATCGCTTGAGTCCAGGAGGTTGAGGCTGAAGTGAGC T C TSG101 Ensembl:ENSG00000074319 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1268881953 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91752,RMVar_hsa_circ_148606 4678 RMVar_ID_4678 Human_SNP_ID_457741968 A-to-I Human chr11 - 18538421 18538421 18538421 TGATCCCAGCTACTTGGGAGTCTGAGGCGCACACCTGTAATCCCAGCTACTTGGGAGGCTGAGGC TGATCCCAGCTACTTGGGAGTCTGAGGCGCACGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGC T C UEVLD Ensembl:ENSG00000151116 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs545440736 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22884,RMVar_hsa_circ_51744,RMVar_hsa_circ_310912,RMVar_hsa_circ_31982,RMVar_hsa_circ_39972,RMVar_hsa_circ_373938,RMVar_hsa_circ_148615,RMVar_hsa_circ_61518,RMVar_hsa_circ_34836,RMVar_hsa_circ_148616,RMVar_hsa_circ_1392 4679 RMVar_ID_4679 Human_SNP_ID_457746680 A-to-I Human chr11 - 18558621 18558621 18558621 TGCCACCATGCCTGGCTGGTTTTTGTATTTTTAGTAGAGGTGGGGTTTCGCCATGTTGGCCAGGC TGCCACCATGCCTGGCTGGTTTTTGTATTTTTGGTAGAGGTGGGGTTTCGCCATGTTGGCCAGGC T C UEVLD Ensembl:ENSG00000151116 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1020416344 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22884,RMVar_hsa_circ_310912,RMVar_hsa_circ_7528,RMVar_hsa_circ_31982,RMVar_hsa_circ_39972,RMVar_hsa_circ_148615,RMVar_hsa_circ_302152,RMVar_hsa_circ_1392,RMVar_hsa_circ_302480,RMVar_hsa_circ_351473,RMVar_hsa_circ_270818,RMVar_hsa_circ_148620,RMVar_hsa_circ_148617,RMVar_hsa_circ_148618,RMVar_hsa_circ_299398,RMVar_hsa_circ_320706,RMVar_hsa_circ_148622,RMVar_hsa_circ_293522,RMVar_hsa_circ_148621,RMVar_hsa_circ_148626,RMVar_hsa_circ_324173,RMVar_hsa_circ_337039,RMVar_hsa_circ_338059,RMVar_hsa_circ_330791,RMVar_hsa_circ_320256,RMVar_hsa_circ_148624,RMVar_hsa_circ_148625,RMVar_hsa_circ_148623 4680 RMVar_ID_4680 Human_SNP_ID_457756074 A-to-I Human chr11 + 18596110 18596110 18596110 GGAGCTCAGCACACCACTGTACTTAACCTCCCATCCCACAAATTAGACCATGCAGCACATCAAGA GGAGCTCAGCACACCACTGTACTTAACCTCCCGTCCCACAAATTAGACCATGCAGCACATCAAGA A G SPTY2D1OS Ensembl:ENSG00000247595 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs747246619 Functional Loss SNV dbSNP153 33..33 33 - - - 4681 RMVar_ID_4681 Human_SNP_ID_457758071 A-to-I Human chr11 + 18604111 18604111 18604111 ACCACGCCTGGCTATTTTTTTGTGTTTTTAGTAGAGACGGGGTTTCACCGTGTTATCCAGGATGG ACCACGCCTGGCTATTTTTTTGTGTTTTTAGTGGAGACGGGGTTTCACCGTGTTATCCAGGATGG A G SPTY2D1OS Ensembl:ENSG00000247595 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985540066 Functional Loss SNV dbSNP153 33..33 33 - - - 4682 RMVar_ID_4682 Human_SNP_ID_457773690 A-to-I Human chr11 + 18665018 18665018 18665018 AGCAGGAAGGCCCATCGGAGCATGTGGATTTGAGCCACCACATTTTTTAACCCTAGATCTCGAAA AGCAGGAAGGCCCATCGGAGCATGTGGATTTGTGCCACCACATTTTTTAACCCTAGATCTCGAAA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031564862 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22790092,Human_RBP_ID_22896087,Human_RBP_ID_26888759 4683 RMVar_ID_4683 Human_SNP_ID_457773692 A-to-I Human chr11 + 18665022 18665022 18665022 GGAAGGCCCATCGGAGCATGTGGATTTGAGCCACCACATTTTTTAACCCTAGATCTCGAAATGCA GGAAGGCCCATCGGAGCATGTGGATTTGAGCCGCCACATTTTTTAACCCTAGATCTCGAAATGCA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878858042 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22790092,Human_RBP_ID_22896087,Human_RBP_ID_26888759 4684 RMVar_ID_4684 Human_SNP_ID_457773695 A-to-I Human chr11 + 18665025 18665025 18665025 AGGCCCATCGGAGCATGTGGATTTGAGCCACCACATTTTTTAACCCTAGATCTCGAAATGCATCG AGGCCCATCGGAGCATGTGGATTTGAGCCACCGCATTTTTTAACCCTAGATCTCGAAATGCATCG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879228353 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22790092,Human_RBP_ID_22896087,Human_RBP_ID_26402933,Human_RBP_ID_26888759,Human_RBP_ID_27410643 4685 RMVar_ID_4685 Human_SNP_ID_457773768 A-to-I Human chr11 - 18665279 18665279 18665279 TTTTTCACCATTGGACAGTTCCACTCTTACACAGCAGCCACATAGTGTTCTTCCATTTAGCTCTC TTTTTCACCATTGGACAGTTCCACTCTTACACGGCAGCCACATAGTGTTCTTCCATTTAGCTCTC T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs879073273 Functional Loss SNV dbSNP153 33..33 33 - - - 4686 RMVar_ID_4686 Human_SNP_ID_457900027 A-to-I Human chr11 + 19159613 19159613 19159613 TATTTCATCCCATTTCCTTTTTAAAAAATTTTAATCATGGCCCATTTAATTCTTTCATGACTCAC TATTTCATCCCATTTCCTTTTTAAAAAATTTTGATCATGGCCCATTTAATTCTTTCATGACTCAC A G ZDHHC13 Ensembl:ENSG00000177054 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1445416010 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6061722 RMVar_hsa_circ_13203,RMVar_hsa_circ_315499,RMVar_hsa_circ_148639,RMVar_hsa_circ_112477,RMVar_hsa_circ_76783,RMVar_hsa_circ_35545,RMVar_hsa_circ_148640,RMVar_hsa_circ_148642,RMVar_hsa_circ_323621,RMVar_hsa_circ_148641,RMVar_hsa_circ_148643 4687 RMVar_ID_4687 Human_SNP_ID_457900040 A-to-I Human chr11 + 19159654 19159654 19159654 CCATTTAATTCTTTCATGACTCACTAATGAATAGCAGCCTGAGATTAAAACAAAAACAAACAAAC CCATTTAATTCTTTCATGACTCACTAATGAATTGCAGCCTGAGATTAAAACAAAAACAAACAAAC A T ZDHHC13 Ensembl:ENSG00000177054 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1236376551 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13203,RMVar_hsa_circ_315499,RMVar_hsa_circ_148639,RMVar_hsa_circ_112477,RMVar_hsa_circ_76783,RMVar_hsa_circ_35545,RMVar_hsa_circ_148640,RMVar_hsa_circ_148642,RMVar_hsa_circ_323621,RMVar_hsa_circ_148641,RMVar_hsa_circ_148643 4688 RMVar_ID_4688 Human_SNP_ID_457900063 A-to-I Human chr11 - 19159761 19159761 19159761 GGTGACAGGACTTGGCCAACACTAAGAGAACAACACACCCCTAAGCTGGACTTGGTCCTGGGCCC GGTGACAGGACTTGGCCAACACTAAGAGAACAGCACACCCCTAAGCTGGACTTGGTCCTGGGCCC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1362174132 Functional Loss SNV dbSNP153 33..33 33 - - - 4689 RMVar_ID_4689 Human_SNP_ID_457900247 A-to-I Human chr11 + 19160687 19160687 19160687 TGTAGAATCAAAGTCATAAATGGTTACAACCCAAGTAACCCCTCTCCCCATTTCTAGGTGACAGG TGTAGAATCAAAGTCATAAATGGTTACAACCCTAGTAACCCCTCTCCCCATTTCTAGGTGACAGG A T ZDHHC13 Ensembl:ENSG00000177054 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1259374616 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13203,RMVar_hsa_circ_315499,RMVar_hsa_circ_148639,RMVar_hsa_circ_112477,RMVar_hsa_circ_76783,RMVar_hsa_circ_35545,RMVar_hsa_circ_148640,RMVar_hsa_circ_148642,RMVar_hsa_circ_323621,RMVar_hsa_circ_148641,RMVar_hsa_circ_148643 4690 RMVar_ID_4690 Human_SNP_ID_457900285 A-to-I Human chr11 + 19160834 19160834 19160834 TTGGATGAGTTTTTTTTGTTTGTTTTTGTTTTAATCTCAGACTGCTATTCGTTAGTGGGTCGTGG TTGGATGAGTTTTTTTTGTTTGTTTTTGTTTTGATCTCAGACTGCTATTCGTTAGTGGGTCGTGG A G ZDHHC13 Ensembl:ENSG00000177054 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1308378300 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6061726 RMVar_hsa_circ_13203,RMVar_hsa_circ_315499,RMVar_hsa_circ_148639,RMVar_hsa_circ_112477,RMVar_hsa_circ_76783,RMVar_hsa_circ_35545,RMVar_hsa_circ_148640,RMVar_hsa_circ_148642,RMVar_hsa_circ_323621,RMVar_hsa_circ_148641,RMVar_hsa_circ_148643 4691 RMVar_ID_4691 Human_SNP_ID_457900290 A-to-I Human chr11 + 19160855 19160855 19160855 GTTTTTGTTTTAATCTCAGACTGCTATTCGTTAGTGGGTCGTGGAAGAATTAAATGGGCCGTGAT GTTTTTGTTTTAATCTCAGACTGCTATTCGTTGGTGGGTCGTGGAAGAATTAAATGGGCCGTGAT A G ZDHHC13 Ensembl:ENSG00000177054 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs769295563 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13203,RMVar_hsa_circ_315499,RMVar_hsa_circ_148639,RMVar_hsa_circ_112477,RMVar_hsa_circ_76783,RMVar_hsa_circ_35545,RMVar_hsa_circ_148640,RMVar_hsa_circ_148642,RMVar_hsa_circ_323621,RMVar_hsa_circ_148641,RMVar_hsa_circ_148643 4692 RMVar_ID_4692 Human_SNP_ID_457900291 A-to-I Human chr11 + 19160855 19160855 19160855 GTTTTTGTTTTAATCTCAGACTGCTATTCGTTAGTGGGTCGTGGAAGAATTAAATGGGCCGTGAT GTTTTTGTTTTAATCTCAGACTGCTATTCGTTTGTGGGTCGTGGAAGAATTAAATGGGCCGTGAT A T ZDHHC13 Ensembl:ENSG00000177054 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs769295563 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13203,RMVar_hsa_circ_315499,RMVar_hsa_circ_148639,RMVar_hsa_circ_112477,RMVar_hsa_circ_76783,RMVar_hsa_circ_35545,RMVar_hsa_circ_148640,RMVar_hsa_circ_148642,RMVar_hsa_circ_323621,RMVar_hsa_circ_148641,RMVar_hsa_circ_148643 4693 RMVar_ID_4693 Human_SNP_ID_457928755 A-to-I Human chr11 - 19274877 19274876 19274878 TTGGATGTTGAACAACTTGGAATTCCAAAACAAGAGTACAGCTGTGTAGTAAAGATGCCTGCTGG TTGGATGTTGAACAACTTGGAATTCCAAAAC__GAGTACAGCTGTGTAGTAAAGATGCCTGCTGG CTT C PCNAP4 Ensembl:ENSG00000254544 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1262587425 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_26410420 4694 RMVar_ID_4694 Human_SNP_ID_458054445 A-to-I Human chr11 + 19787390 19787390 19787390 CTTCTGCCTCAGCCTCCTAAAGTGTTGGGATTACAGACGTGAACCACTGCACCCGGTAGAGTGCT CTTCTGCCTCAGCCTCCTAAAGTGTTGGGATTGCAGACGTGAACCACTGCACCCGGTAGAGTGCT A G NAV2 Ensembl:ENSG00000166833 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs758492156 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107272,RMVar_hsa_circ_148647 4695 RMVar_ID_4695 Human_SNP_ID_458054446 A-to-I Human chr11 + 19787390 19787390 19787390 CTTCTGCCTCAGCCTCCTAAAGTGTTGGGATTACAGACGTGAACCACTGCACCCGGTAGAGTGCT CTTCTGCCTCAGCCTCCTAAAGTGTTGGGATTTCAGACGTGAACCACTGCACCCGGTAGAGTGCT A T NAV2 Ensembl:ENSG00000166833 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs758492156 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107272,RMVar_hsa_circ_148647 4696 RMVar_ID_4696 Human_SNP_ID_458100254 A-to-I Human chr11 + 19970443 19970443 19970443 CATTTGCCTCAGCCTCCCAAAGTGCTGAGATTACAGGCACTGCACCCAGTCCAACAATTTAATTG CATTTGCCTCAGCCTCCCAAAGTGCTGAGATTGCAGGCACTGCACCCAGTCCAACAATTTAATTG A G NAV2 Ensembl:ENSG00000166833 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1330943270 Functional Loss SNV dbSNP153 33..33 33 - - - 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_13725,RMVar_hsa_circ_94749,RMVar_hsa_circ_148658,RMVar_hsa_circ_23139,RMVar_hsa_circ_100448,RMVar_hsa_circ_148660,RMVar_hsa_circ_20504,RMVar_hsa_circ_325778,RMVar_hsa_circ_148662,RMVar_hsa_circ_83061,RMVar_hsa_circ_148663 4697 RMVar_ID_4697 Human_SNP_ID_212147782 A-to-I Human chr4 - 165075212 165075212 165075212 AAAGAAAAGAAAAAAAATTGTATTTCTAGTAGAGACGGGGATTCACCATGTTGGCCAGGCTGATC AAAGAAAAGAAAAAAAATTGTATTTCTAGTAGCGACGGGGATTCACCATGTTGGCCAGGCTGATC T G TMEM192 Ensembl:ENSG00000170088 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1377863059 Functional Loss SNV dbSNP153 33..33 33 - - - 4698 RMVar_ID_4698 Human_SNP_ID_212147784 A-to-I Human chr4 - 165075217 165075217 165075217 AAAAGAAAGAAAAGAAAAAAAATTGTATTTCTAGTAGAGACGGGGATTCACCATGTTGGCCAGGC AAAAGAAAGAAAAGAAAAAAAATTGTATTTCTTGTAGAGACGGGGATTCACCATGTTGGCCAGGC T A TMEM192 Ensembl:ENSG00000170088 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971457146 Functional Loss SNV dbSNP153 33..33 33 - - - 4699 RMVar_ID_4699 Human_SNP_ID_212147909 A-to-I Human chr4 - 165075632 165075632 165075632 CCAGCAGGTGGAGGTTGCAGTGAGGCAAGATCACGCCACTGTACTCTAGCCTGGGCCACAGAGCA CCAGCAGGTGGAGGTTGCAGTGAGGCAAGATCCCGCCACTGTACTCTAGCCTGGGCCACAGAGCA T G TMEM192 Ensembl:ENSG00000170088 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1398478754 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_615954,Human_RBP_ID_15088567 4700 RMVar_ID_4700 Human_SNP_ID_212147929 A-to-I Human chr4 - 165075686 165075686 165075686 GGGTGCCTGTAATCCCAGCTACTCTGGAGGCTAAGGCAGGAGAATTGCTTGAACCCAGCAGGTGG GGGTGCCTGTAATCCCAGCTACTCTGGAGGCTGAGGCAGGAGAATTGCTTGAACCCAGCAGGTGG T C TMEM192 Ensembl:ENSG00000170088 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1466254610 Functional Loss SNV dbSNP153 33..33 33 - - - 4701 RMVar_ID_4701 Human_SNP_ID_212147959 A-to-I Human chr4 - 165075790 165075790 165075790 GCCAAGGTGGGTGGATCACAAGGTCAGGAGTTAGAGACCAGCCTGGCCAAGATGGTGAAACCCCA GCCAAGGTGGGTGGATCACAAGGTCAGGAGTTCGAGACCAGCCTGGCCAAGATGGTGAAACCCCA T G TMEM192 Ensembl:ENSG00000170088 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1339140429 Functional Loss SNV dbSNP153 33..33 33 - - - 4702 RMVar_ID_4702 Human_SNP_ID_212147972 A-to-I Human chr4 - 165075838 165075838 165075838 TTGGGTCGGGTGTGGTAGCTTACGCCTGTAATACCAGCACTTTGGGAGGCCAAGGTGGGTGGATC TTGGGTCGGGTGTGGTAGCTTACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGTGGATC T G TMEM192 Ensembl:ENSG00000170088 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1001779416 Functional Loss SNV dbSNP153 33..33 33 - - - 4703 RMVar_ID_4703 Human_SNP_ID_212147973 A-to-I Human chr4 - 165075840 165075840 165075840 ATTTGGGTCGGGTGTGGTAGCTTACGCCTGTAATACCAGCACTTTGGGAGGCCAAGGTGGGTGGA ATTTGGGTCGGGTGTGGTAGCTTACGCCTGTAGTACCAGCACTTTGGGAGGCCAAGGTGGGTGGA T C TMEM192 Ensembl:ENSG00000170088 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6821749 Functional Loss SNV dbSNP153 33..33 33 - - - 4704 RMVar_ID_4704 Human_SNP_ID_212147977 A-to-I Human chr4 - 165075849 165075849 165075849 ATATTAAAAATTTGGGTCGGGTGTGGTAGCTTACGCCTGTAATACCAGCACTTTGGGAGGCCAAG ATATTAAAAATTTGGGTCGGGTGTGGTAGCTTGCGCCTGTAATACCAGCACTTTGGGAGGCCAAG T C TMEM192 Ensembl:ENSG00000170088 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs539983632 Functional Loss SNV dbSNP153 33..33 33 - - - 4705 RMVar_ID_4705 Human_SNP_ID_212147978 A-to-I Human chr4 - 165075854 165075854 165075854 CAAAAATATTAAAAATTTGGGTCGGGTGTGGTAGCTTACGCCTGTAATACCAGCACTTTGGGAGG CAAAAATATTAAAAATTTGGGTCGGGTGTGGTGGCTTACGCCTGTAATACCAGCACTTTGGGAGG T C TMEM192 Ensembl:ENSG00000170088 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1354655364 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_615955,Human_RBP_ID_18021448 4706 RMVar_ID_4706 Human_SNP_ID_212148008 A-to-I Human chr4 - 165076020 165076020 165076020 ACTTTTTTTGTTTTGTTTTTTTTTTTAGTCTCATCTGTCTCCCAGGCTGGAGTGCAGTGGTGTGA ACTTTTTTTGTTTTGTTTTTTTTTTTAGTCTCTTCTGTCTCCCAGGCTGGAGTGCAGTGGTGTGA T A TMEM192 Ensembl:ENSG00000170088 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1043182595 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5448437,Human_RBP_ID_7285025 4707 RMVar_ID_4707 Human_SNP_ID_212148182 A-to-I Human chr4 - 165076859 165076859 165076859 AGGCAGAGGTTGCAGTGAGCTGAAATTGCACCACTGCATTCCAGCTTGGGCAACAGAGCTAGACT AGGCAGAGGTTGCAGTGAGCTGAAATTGCACCGCTGCATTCCAGCTTGGGCAACAGAGCTAGACT T C TMEM192 Ensembl:ENSG00000170088 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1456939099 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26514026 RMVar_hsa_circ_105236,RMVar_hsa_circ_229407 4708 RMVar_ID_4708 Human_SNP_ID_212148198 A-to-I Human chr4 - 165076939 165076939 165076939 AAATAAGCCAGGCATGGTGGCACGCATCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAA AAATAAGCCAGGCATGGTGGCACGCATCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAA T C TMEM192 Ensembl:ENSG00000170088 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs566235595 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105236,RMVar_hsa_circ_229407 4709 RMVar_ID_4709 Human_SNP_ID_212148199 A-to-I Human chr4 - 165076940 165076940 165076940 AAAATAAGCCAGGCATGGTGGCACGCATCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA AAAATAAGCCAGGCATGGTGGCACGCATCTGTTATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA T A TMEM192 Ensembl:ENSG00000170088 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1326738122 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105236,RMVar_hsa_circ_229407 4710 RMVar_ID_4710 Human_SNP_ID_212148209 A-to-I Human chr4 - 165077004 165077003 165077004 CTGAGGTTAGGAGCTCAAGACCAGCCTGGCCAACATAGTAAAACCCCATCTTTACTAAAAATACA CTGAGGTTAGGAGCTCAAGACCAGCCTGGCCA_CATAGTAAAACCCCATCTTTACTAAAAATACA GT G TMEM192 Ensembl:ENSG00000170088 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1230717427 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_105236,RMVar_hsa_circ_229407 4711 RMVar_ID_4711 Human_SNP_ID_212148284 A-to-I Human chr4 - 165077484 165077484 165077484 CCTTGGCCTCCCAAAGTGTTGGGATTACAGGCATGAGCCACTGTGCCCGGCCTTCCTTTCTTTTT CCTTGGCCTCCCAAAGTGTTGGGATTACAGGCGTGAGCCACTGTGCCCGGCCTTCCTTTCTTTTT T C TMEM192 Ensembl:ENSG00000170088 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1475836535 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26518524 Human_miRNA_ID_1698533,Human_miRNA_ID_1994914,Human_miRNA_ID_2227411,Human_miRNA_ID_2503388 RMVar_hsa_circ_105236,RMVar_hsa_circ_229407 4712 RMVar_ID_4712 Human_SNP_ID_212148300 A-to-I Human chr4 - 165077562 165077562 165077562 TTTTGTATTTTTAGTACAGGCGGGGTTTCACCATGCTGGCCAGGCTGGTCTCAAACTCCTGACCT TTTTGTATTTTTAGTACAGGCGGGGTTTCACCGTGCTGGCCAGGCTGGTCTCAAACTCCTGACCT T C TMEM192 Ensembl:ENSG00000170088 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs572582944 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_972732,Human_miRNA_ID_2440760 RMVar_hsa_circ_105236,RMVar_hsa_circ_229407 4713 RMVar_ID_4713 Human_SNP_ID_212148314 A-to-I Human chr4 - 165077621 165077621 165077621 CCTACCTCAGCCTGCTGAGTAGCTGGGATTACAGGCACATGCCACCATGCCTGGCTAATTTTTGT CCTACCTCAGCCTGCTGAGTAGCTGGGATTACGGGCACATGCCACCATGCCTGGCTAATTTTTGT T C TMEM192 Ensembl:ENSG00000170088 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs777151102 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105236,RMVar_hsa_circ_229407 4714 RMVar_ID_4714 Human_SNP_ID_212148372 A-to-I Human chr4 - 165077798 165077797 165077798 TTTTTTTGTTGTTGTTTTTGAGACAGAGTCTCACCCTGTCGCCCAGGCTGGAGTGCAATGGCGCC TTTTTTTGTTGTTGTTTTTGAGACAGAGTCTC_CCCTGTCGCCCAGGCTGGAGTGCAATGGCGCC GT G TMEM192 Ensembl:ENSG00000170088 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1184479775 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_105236,RMVar_hsa_circ_229407 4715 RMVar_ID_4715 Human_SNP_ID_212148445 A-to-I Human chr4 - 165078036 165078036 165078036 TGTATGGCTGGGAGCAGTTGCTCATGCCTGTAATCTTAGTACTTTGGGAGGCTGAGGCAGGAGGA TGTATGGCTGGGAGCAGTTGCTCATGCCTGTAGTCTTAGTACTTTGGGAGGCTGAGGCAGGAGGA T C TMEM192 Ensembl:ENSG00000170088 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1133361 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8212476,Human_RBP_ID_24043723,Human_RBP_ID_26514035 RMVar_hsa_circ_105236,RMVar_hsa_circ_229407 4716 RMVar_ID_4716 Human_SNP_ID_212148610 A-to-I Human chr4 - 165078882 165078882 165078882 GGGAGGCTGAGGCAGGAGAATGGTGTGGACCCAGGAGGCGGAGCTTGCAGTGAGCCGAGATCACG GGGAGGCTGAGGCAGGAGAATGGTGTGGACCCGGGAGGCGGAGCTTGCAGTGAGCCGAGATCACG T C TMEM192 Ensembl:ENSG00000170088 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs957682021 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105236,RMVar_hsa_circ_229407 4717 RMVar_ID_4717 Human_SNP_ID_212150213 A-to-I Human chr4 - 165086616 165086616 165086616 GTTTGAGAACAGCCTGGCCAACATGGTGAAACACCGTCTCTACTGAAAATACAAAAAAAATTAGC GTTTGAGAACAGCCTGGCCAACATGGTGAAACGCCGTCTCTACTGAAAATACAAAAAAAATTAGC T C TMEM192 Ensembl:ENSG00000170088 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1383125698 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105236,RMVar_hsa_circ_229410,RMVar_hsa_circ_229408,RMVar_hsa_circ_229407,RMVar_hsa_circ_300512,RMVar_hsa_circ_307905,RMVar_hsa_circ_338285,RMVar_hsa_circ_229411,RMVar_hsa_circ_229409 4718 RMVar_ID_4718 Human_SNP_ID_212150273 A-to-I Human chr4 - 165086857 165086857 165086857 TATCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGACATGAGCCACCATGCCCAGCCTGAAAGG TATCCGCCTCGGCCTCCCAAAGTGCTGGGATTGCAGACATGAGCCACCATGCCCAGCCTGAAAGG T C TMEM192 Ensembl:ENSG00000170088 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1268932911 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105236,RMVar_hsa_circ_229410,RMVar_hsa_circ_229408,RMVar_hsa_circ_229407,RMVar_hsa_circ_300512,RMVar_hsa_circ_307905,RMVar_hsa_circ_338285,RMVar_hsa_circ_229411,RMVar_hsa_circ_229409 4719 RMVar_ID_4719 Human_SNP_ID_212185351 A-to-I Human chr4 + 165235466 165235466 165235466 CACATGATCCGCCTGCCTTGGCCTCCCAAAGCACTGGGATTACAGGCATGAGCCCCTGTGCCCAG CACATGATCCGCCTGCCTTGGCCTCCCAAAGCGCTGGGATTACAGGCATGAGCCCCTGTGCCCAG A G KLHL2 Ensembl:ENSG00000109466 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1350113988 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127439,RMVar_hsa_circ_76353,RMVar_hsa_circ_279388,RMVar_hsa_circ_62935,RMVar_hsa_circ_229416,RMVar_hsa_circ_77607,RMVar_hsa_circ_229415,RMVar_hsa_circ_352869,RMVar_hsa_circ_372529,RMVar_hsa_circ_110079,RMVar_hsa_circ_276297,RMVar_hsa_circ_85079,RMVar_hsa_circ_123477,RMVar_hsa_circ_229418,RMVar_hsa_circ_229420,RMVar_hsa_circ_229422,RMVar_hsa_circ_229421,RMVar_hsa_circ_229419,RMVar_hsa_circ_229417,RMVar_hsa_circ_318327,RMVar_hsa_circ_58829,RMVar_hsa_circ_229425 4720 RMVar_ID_4720 Human_SNP_ID_212207496 A-to-I Human chr4 + 165331046 165331046 165331046 AAGATGTAGGCTGGGCGCAGTGGCTCACACCTATAATCCCCACACTTTGGGAGGCTGAGATGGGA AAGATGTAGGCTGGGCGCAGTGGCTCACACCTGTAATCCCCACACTTTGGGAGGCTGAGATGGGA A G MSMO1 Ensembl:ENSG00000052802 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs546701041 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25790012 RMVar_hsa_circ_100844,RMVar_hsa_circ_229435 4721 RMVar_ID_4721 Human_SNP_ID_212207518 A-to-I Human chr4 + 165331155 165331155 165331155 GGGTGACCCCTGTCTCCACAAAAAATTAAAAAAATTAGCCAGGCGTGGTGGCATGTGCCTGTGGT GGGTGACCCCTGTCTCCACAAAAAATTAAAAACATTAGCCAGGCGTGGTGGCATGTGCCTGTGGT A C MSMO1 Ensembl:ENSG00000052802 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs931265002 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100844,RMVar_hsa_circ_229435 4722 RMVar_ID_4722 Human_SNP_ID_212210415 A-to-I Human chr4 + 165342639 165342639 165342639 TTGGCCTCCCAAAGTGCTGGGATTACAGGTGTAAGCCACTGCGCCCGGCCTTTTTAACTTTAAAC TTGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACTGCGCCCGGCCTTTTTAACTTTAAAC A G MSMO1 Ensembl:ENSG00000052802 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs536090786 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15237751,Human_RBP_ID_17409388,Human_RBP_ID_17525625 RMVar_hsa_circ_100844,RMVar_hsa_circ_229435,RMVar_hsa_circ_110729,RMVar_hsa_circ_229437 4723 RMVar_ID_4723 Human_SNP_ID_212225090 A-to-I Human chr4 - 165405568 165405568 165405568 TCTCCAAAGAGAGACAAGGGATTAGTGGAAAAATTAACAGCGTATGCCATGACTATTCCATTTGT TCTCCAAAGAGAGACAAGGGATTAGTGGAAAACTTAACAGCGTATGCCATGACTATTCCATTTGT T G HADHAP1 Ensembl:ENSG00000251596 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1490805032 Functional Loss SNV dbSNP153 33..33 33 - - - 4724 RMVar_ID_4724 Human_SNP_ID_212348949 A-to-I Human chr4 + 165908476 165908476 165908476 GCGGTGACATTTGCCTGTAGTCCCAGCTACTCAGGAGACTGAGGTGAGAGGATCACCTGAGCCTG GCGGTGACATTTGCCTGTAGTCCCAGCTACTCCGGAGACTGAGGTGAGAGGATCACCTGAGCCTG A C TLL1 Ensembl:ENSG00000038295 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1266672683 Functional Loss SNV dbSNP153 33..33 33 - - - 4725 RMVar_ID_4725 Human_SNP_ID_212371730 A-to-I Human chr4 + 166002713 166002713 166002713 ACAGTCCTCCCAGGTTGGCCTTCCGAAGTGCTAGGATTACAGGCATGAGCCACTGCAACCAGCCA ACAGTCCTCCCAGGTTGGCCTTCCGAAGTGCTGGGATTACAGGCATGAGCCACTGCAACCAGCCA A G TLL1 Ensembl:ENSG00000038295 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs948098225 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_229442,RMVar_hsa_circ_48616,RMVar_hsa_circ_284061,RMVar_hsa_circ_319193,RMVar_hsa_circ_266255,RMVar_hsa_circ_229443,RMVar_hsa_circ_229441 4726 RMVar_ID_4726 Human_SNP_ID_212375091 A-to-I Human chr4 + 166017104 166017104 166017104 CAACCCTTGCCGCCTCCCACTCCCTCCCCTCTAGTAGTCCATACTGTCTATTGTTCCTGTCTTTA CAACCCTTGCCGCCTCCCACTCCCTCCCCTCTTGTAGTCCATACTGTCTATTGTTCCTGTCTTTA A T TLL1 Ensembl:ENSG00000038295 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs912902261 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_229442,RMVar_hsa_circ_48616,RMVar_hsa_circ_284061,RMVar_hsa_circ_266255,RMVar_hsa_circ_229444,RMVar_hsa_circ_229441,RMVar_hsa_circ_357058,RMVar_hsa_circ_229445,RMVar_hsa_circ_290178 4727 RMVar_ID_4727 Human_SNP_ID_212375463 A-to-I Human chr4 + 166018797 166018797 166018797 CACCAGTCAGAATAGCTGTTATTAAAAAGATGAAAAATGACAGATGCTGCAGAGGCTGTAGAGTA CACCAGTCAGAATAGCTGTTATTAAAAAGATGGAAAATGACAGATGCTGCAGAGGCTGTAGAGTA A G TLL1 Ensembl:ENSG00000038295 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs116304156 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_229442,RMVar_hsa_circ_48616,RMVar_hsa_circ_284061,RMVar_hsa_circ_266255,RMVar_hsa_circ_229444,RMVar_hsa_circ_229441,RMVar_hsa_circ_357058,RMVar_hsa_circ_229445,RMVar_hsa_circ_290178 4728 RMVar_ID_4728 Human_SNP_ID_212375530 A-to-I Human chr4 + 166019158 166019158 166019158 AAAAATAATGAAATCATGTCCTTTTCAGCCGCATGGATGGAGCTGGAGGCCATAATCCTAAATCA AAAAATAATGAAATCATGTCCTTTTCAGCCGCGTGGATGGAGCTGGAGGCCATAATCCTAAATCA A G TLL1 Ensembl:ENSG00000038295 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1287528165 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2829145 RMVar_hsa_circ_229442,RMVar_hsa_circ_48616,RMVar_hsa_circ_284061,RMVar_hsa_circ_266255,RMVar_hsa_circ_229444,RMVar_hsa_circ_229441,RMVar_hsa_circ_357058,RMVar_hsa_circ_229445,RMVar_hsa_circ_290178 4729 RMVar_ID_4729 Human_SNP_ID_212684443 A-to-I Human chr4 - 167221260 167221260 167221260 GGGCTCAAGTGATCCTCCCACTTTCGCTTCTCAAGTAGCTGGGACTACAGGCATGTACCACCATG GGGCTCAAGTGATCCTCCCACTTTCGCTTCTCGAGTAGCTGGGACTACAGGCATGTACCACCATG T C SPOCK3 Ensembl:ENSG00000196104 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1360533924 Functional Loss SNV dbSNP153 33..33 33 - - - 4730 RMVar_ID_4730 Human_SNP_ID_213041912 A-to-I Human chr4 + 168637823 168637823 168637823 AAAATTAGTTGGGCATGGTGGTGAGTACCGGTAATCCCAGCTACCCGGTTGGCTGAGACAGGAGA AAAATTAGTTGGGCATGGTGGTGAGTACCGGTGATCCCAGCTACCCGGTTGGCTGAGACAGGAGA A G PALLD Ensembl:ENSG00000129116 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs942907203 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99022,RMVar_hsa_circ_229474 4731 RMVar_ID_4731 Human_SNP_ID_213067991 A-to-I Human chr4 + 168746274 168746274 168746274 CCTCATCAAGAGGAGGGACTTGACAGCTACTCAGGAGGCTGAGGCAGGAGAATGGCGTGAACCCG CCTCATCAAGAGGAGGGACTTGACAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCG A G PALLD Ensembl:ENSG00000129116 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs902508368 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_369329,RMVar_hsa_circ_229475 4732 RMVar_ID_4732 Human_SNP_ID_213068776 A-to-I Human chr4 + 168749599 168749599 168749599 CATCATGGGCACCTGTAATCCCAGATACTCAGAAGGCTAAGGCAGGAGAATCACTTGAACCCGAG CATCATGGGCACCTGTAATCCCAGATACTCAGCAGGCTAAGGCAGGAGAATCACTTGAACCCGAG A C PALLD Ensembl:ENSG00000129116 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1379581639 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_369329,RMVar_hsa_circ_229475 4733 RMVar_ID_4733 Human_SNP_ID_213125250 A-to-I Human chr4 - 168990528 168990528 168990528 GGAGGCTGAGGCAAGAGGATCACCTGTGCCCCAGAGGTCCAGGCTGCAGTGAGTCGTGTTTGCAC GGAGGCTGAGGCAAGAGGATCACCTGTGCCCCCGAGGTCCAGGCTGCAGTGAGTCGTGTTTGCAC T G CBR4 Ensembl:ENSG00000145439 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1263987086 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17574908 4734 RMVar_ID_4734 Human_SNP_ID_213125341 A-to-I Human chr4 - 168990916 168990916 168990916 CTGAGTAGCTGGGATTACAGGCGTCCACCACCACCCCCAGCTAATTTTTTGTATTTTTAGTAGAG CTGAGTAGCTGGGATTACAGGCGTCCACCACCCCCCCCAGCTAATTTTTTGTATTTTTAGTAGAG T G CBR4 Ensembl:ENSG00000145439 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs368726699 Functional Loss SNV dbSNP153 33..33 33 - - - 4735 RMVar_ID_4735 Human_SNP_ID_213128496 A-to-I Human chr4 - 169003524 169003524 169003524 CAATCCCTGCTATTGCTTTATCAACTAAGTTTATAGGATATTCTAAATCCTTTGTCATTTCTTTC CAATCCCTGCTATTGCTTTATCAACTAAGTTTGTAGGATATTCTAAATCCTTTGTCATTTCTTTC T C CBR4 Ensembl:ENSG00000145439 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1390429209 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85493,RMVar_hsa_circ_121078,RMVar_hsa_circ_229488,RMVar_hsa_circ_272637,RMVar_hsa_circ_229489,RMVar_hsa_circ_366223,RMVar_hsa_circ_229491,RMVar_hsa_circ_229492 4736 RMVar_ID_4736 Human_SNP_ID_213184228 A-to-I Human chr4 - 169239899 169239899 169239899 CTGCCTCAGCCTCCCAAGTAGCTGGGAGTATAAGTGCACACCACCACGCCCGGCTTATTTTTGTA CTGCCTCAGCCTCCCAAGTAGCTGGGAGTATAGGTGCACACCACCACGCCCGGCTTATTTTTGTA T C SH3RF1 Ensembl:ENSG00000154447 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559977855 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69708 4737 RMVar_ID_4737 Human_SNP_ID_213297871 A-to-I Human chr4 + 169720054 169720054 169720054 AAACGGAAGAGGAAGTTTATTTGTTGAATAGCACAACTCTTTAACCTGAGGGAGTCATCTACTTT AAACGGAAGAGGAAGTTTATTTGTTGAATAGCCCAACTCTTTAACCTGAGGGAGTCATCTACTTT A C CLCN3 Ensembl:ENSG00000109572 Protein coding CDS GSE56152 embryonic stem cells,wild type - 25708366 RNA-Seq:(High) rs1223600423 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17662030,Human_RBP_ID_22289021,Human_RBP_ID_27325405,Human_RBP_ID_27824514 Human_miRNA_ID_625916 RMVar_hsa_circ_118088,RMVar_hsa_circ_229544 4738 RMVar_ID_4738 Human_SNP_ID_213325469 A-to-I Human chr4 + 169833014 169833014 169833014 GAATTTAGATTTGTGCCTAGTGATAAATCAACATTGGAGGCAACATTCACTGCAATGTGTGAATG GAATTTAGATTTGTGCCTAGTGATAAATCAACTTTGGAGGCAACATTCACTGCAATGTGTGAATG A T AC079768.1 Ensembl:ENSG00000248625 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1421278204 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1870545,Human_miRNA_ID_1870546 4739 RMVar_ID_4739 Human_SNP_ID_213929416 A-to-I Human chr4 + 172236439 172236439 172236439 AAAATTAGCCAGGCATGGTGGCAGGCACCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA AAAATTAGCCAGGCATGGTGGCAGGCACCTGTGGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA A G GALNTL6 Ensembl:ENSG00000174473 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1435250620 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_297687,RMVar_hsa_circ_349403,RMVar_hsa_circ_46517,RMVar_hsa_circ_229559,RMVar_hsa_circ_10649 4740 RMVar_ID_4740 Human_SNP_ID_213929421 A-to-I Human chr4 + 172236477 172236477 172236477 AGCTACTTGGGAGGCTGAGGCAGGAGAATGGCATGAACCCGGGAGGCAGGGCTTGCAGTGAGCCA AGCTACTTGGGAGGCTGAGGCAGGAGAATGGCCTGAACCCGGGAGGCAGGGCTTGCAGTGAGCCA A C GALNTL6 Ensembl:ENSG00000174473 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1023280643 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_297687,RMVar_hsa_circ_349403,RMVar_hsa_circ_46517,RMVar_hsa_circ_229559,RMVar_hsa_circ_10649 4741 RMVar_ID_4741 Human_SNP_ID_214144363 A-to-I Human chr4 - 173158636 173158636 173158636 CCAGGACGCAGAGGTGGCAGTGAGCCGAGATCACGCCCCTGCACTCCAGCCTGGGTGGCAGAGCA CCAGGACGCAGAGGTGGCAGTGAGCCGAGATCGCGCCCCTGCACTCCAGCCTGGGTGGCAGAGCA T C AC105285.1 Ensembl:ENSG00000245213 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1250375142 Functional Loss SNV dbSNP153 33..33 33 - - - 4742 RMVar_ID_4742 Human_SNP_ID_214146059 A-to-I Human chr4 - 173166326 173166326 173166326 AGCTAGGACCACATGTGTGAGTCATCATGCCCAGCTAATTTTTTTTTTATTTTTTGTAGAGACGG AGCTAGGACCACATGTGTGAGTCATCATGCCCGGCTAATTTTTTTTTTATTTTTTGTAGAGACGG T C AC105285.1 Ensembl:ENSG00000245213 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs773496623 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1022 4743 RMVar_ID_4743 Human_SNP_ID_214156879 A-to-I Human chr4 + 173210010 173210010 173210010 CAAAAATTAGCTGGGGGTAGAGGTGCGTGCCTATACTCCCAGCTACTCAGGAAGCCGAGGCAGGA CAAAAATTAGCTGGGGGTAGAGGTGCGTGCCTGTACTCCCAGCTACTCAGGAAGCCGAGGCAGGA A G GALNT7 Ensembl:ENSG00000109586 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs374287734 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_229566,RMVar_hsa_circ_75719 4744 RMVar_ID_4744 Human_SNP_ID_214180137 A-to-I Human chr4 - 173314042 173314042 173314042 TCGAAATTTTTTCAGCTCCGATATATCCCCATATGGTAATGCCTGCGATTCAGGACGACTAGCAT TCGAAATTTTTTCAGCTCCGATATATCCCCATGTGGTAATGCCTGCGATTCAGGACGACTAGCAT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170343635 Functional Loss SNV dbSNP153 33..33 33 - - - 4745 RMVar_ID_4745 Human_SNP_ID_214183354 A-to-I Human chr4 - 173328734 173328734 173328734 ATGGTGGTGCATGCCTGTGGTCCTGGCTATTTAGGAGGCTGAGGTGGATCACTTGAGCCTGGGAT ATGGTGGTGCATGCCTGTGGTCCTGGCTATTTGGGAGGCTGAGGTGGATCACTTGAGCCTGGGAT T C AC097534.1 Ensembl:ENSG00000248774 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1490209946 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7287694 4746 RMVar_ID_4746 Human_SNP_ID_214183416 A-to-I Human chr4 - 173328974 173328974 173328974 GGTTCACGCCATTCTCCTGCTACAGCCTCCCAAGTATCTGGGACTACAGGCGCCCACCACCAAGC GGTTCACGCCATTCTCCTGCTACAGCCTCCCAGGTATCTGGGACTACAGGCGCCCACCACCAAGC T C AC097534.1 Ensembl:ENSG00000248774 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs933561271 Functional Loss SNV dbSNP153 33..33 33 - - - 4747 RMVar_ID_4747 Human_SNP_ID_214202193 A-to-I Human chr4 + 173408846 173408846 173408846 AAACCCCGTCTCTACTAAAAATACAAAAAATTAGCCGGATGTGGTGGCGGGCGCCTGTGGTCCCA AAACCCCGTCTCTACTAAAAATACAAAAAATTGGCCGGATGTGGTGGCGGGCGCCTGTGGTCCCA A G AC093849.4 Ensembl:ENSG00000288025 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1346938790 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_229583,RMVar_hsa_circ_229584 4748 RMVar_ID_4748 Human_SNP_ID_214409774 A-to-I Human chr4 - 174234792 174234792 174234792 CAGGAGTTTCAGACCAGCCTGGGCAACATAGTAAGACCACATTTCTTGCTTAACCAGGATGGTCT CAGGAGTTTCAGACCAGCCTGGGCAACATAGTTAGACCACATTTCTTGCTTAACCAGGATGGTCT T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs773166752 Functional Loss SNV dbSNP153 33..33 33 - - - 4749 RMVar_ID_4749 Human_SNP_ID_214409944 A-to-I Human chr4 - 174235424 174235424 174235424 TACTCAGGAGGCTGAGGCAGGAGGATGGCCTGAGCCCAGGAGTTCGAGATTGCAGTGAGCTGTGA TACTCAGGAGGCTGAGGCAGGAGGATGGCCTGGGCCCAGGAGTTCGAGATTGCAGTGAGCTGTGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1306361433 Functional Loss SNV dbSNP153 33..33 33 - - - 4750 RMVar_ID_4750 Human_SNP_ID_214768642 A-to-I Human chr4 - 175690750 175690750 175690750 GAAGTTGTGATTACATTCAGAATCCTGAGGTGAGCAGATCCTCCTGGATTATCTGGATGAGCCCC GAAGTTGTGATTACATTCAGAATCCTGAGGTGGGCAGATCCTCCTGGATTATCTGGATGAGCCCC T C GPM6A Ensembl:ENSG00000150625 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1442720748 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_319988,RMVar_hsa_circ_229606,RMVar_hsa_circ_12964 4751 RMVar_ID_4751 Human_SNP_ID_214768894 A-to-I Human chr4 - 175691813 175691813 175691813 TAAGGATTCTTGTGATTACAATGGGGCTACCCAGATAATCCAGGGTAATCTCCTCACCTCAATAT TAAGGATTCTTGTGATTACAATGGGGCTACCCTGATAATCCAGGGTAATCTCCTCACCTCAATAT T A GPM6A Ensembl:ENSG00000150625 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1322290147 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_319988,RMVar_hsa_circ_229606,RMVar_hsa_circ_12964 4752 RMVar_ID_4752 Human_SNP_ID_214768895 A-to-I Human chr4 - 175691813 175691813 175691813 TAAGGATTCTTGTGATTACAATGGGGCTACCCAGATAATCCAGGGTAATCTCCTCACCTCAATAT TAAGGATTCTTGTGATTACAATGGGGCTACCCGGATAATCCAGGGTAATCTCCTCACCTCAATAT T C GPM6A Ensembl:ENSG00000150625 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1322290147 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_319988,RMVar_hsa_circ_229606,RMVar_hsa_circ_12964 4753 RMVar_ID_4753 Human_SNP_ID_214778594 A-to-I Human chr4 - 175730753 175730753 175730753 GAGATCGAGAACGGCCAGCAGCGGTGGCTCACACCTGGAATCTCAGCACTTTGGGAGGCCGAGGC GAGATCGAGAACGGCCAGCAGCGGTGGCTCACGCCTGGAATCTCAGCACTTTGGGAGGCCGAGGC T C GPM6A Ensembl:ENSG00000150625 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1284707337 Functional Loss SNV dbSNP153 33..33 33 - - - 4754 RMVar_ID_4754 Human_SNP_ID_214782682 A-to-I Human chr4 - 175747223 175747223 175747223 GCTCTGTCACCAAGCTGGAGTGTAGTGACACAATCTCGGCTAACTGCAACTTCTGCCACCTCGGT GCTCTGTCACCAAGCTGGAGTGTAGTGACACAGTCTCGGCTAACTGCAACTTCTGCCACCTCGGT T C GPM6A Ensembl:ENSG00000150625 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs538492782 Functional Loss SNV dbSNP153 33..33 33 - - - 4755 RMVar_ID_4755 Human_SNP_ID_214782683 A-to-I Human chr4 - 175747223 175747223 175747223 GCTCTGTCACCAAGCTGGAGTGTAGTGACACAATCTCGGCTAACTGCAACTTCTGCCACCTCGGT GCTCTGTCACCAAGCTGGAGTGTAGTGACACACTCTCGGCTAACTGCAACTTCTGCCACCTCGGT T G GPM6A Ensembl:ENSG00000150625 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs538492782 Functional Loss SNV dbSNP153 33..33 33 - - - 4756 RMVar_ID_4756 Human_SNP_ID_214787884 A-to-I Human chr4 - 175768839 175768839 175768839 CACCCACCTCGGCCTCCCAAACTGCTGAGATTACAGATGTGAGCCACCGTACCCGGCCAGGATAG CACCCACCTCGGCCTCCCAAACTGCTGAGATTGCAGATGTGAGCCACCGTACCCGGCCAGGATAG T C GPM6A Ensembl:ENSG00000150625 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs554612366 Functional Loss SNV dbSNP153 33..33 33 - - - 4757 RMVar_ID_4757 Human_SNP_ID_214787907 A-to-I Human chr4 - 175768916 175768916 175768916 TAATTTTGGTATTTTTGTAGAGATGGAGTTTCACCTTGTTGGCCAGGCTGGTCTTGAACTCCTGA TAATTTTGGTATTTTTGTAGAGATGGAGTTTCGCCTTGTTGGCCAGGCTGGTCTTGAACTCCTGA T C GPM6A Ensembl:ENSG00000150625 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1430040766 Functional Loss SNV dbSNP153 33..33 33 - - - 4758 RMVar_ID_4758 Human_SNP_ID_214787925 A-to-I Human chr4 - 175768973 175768973 175768973 CTCCTGCCTCAGCCTCCTGAATAGCTGGGATTACAGGCGCCCACCACCACGCCCAGCTAATTTTG CTCCTGCCTCAGCCTCCTGAATAGCTGGGATTGCAGGCGCCCACCACCACGCCCAGCTAATTTTG T C GPM6A Ensembl:ENSG00000150625 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1026297070 Functional Loss SNV dbSNP153 33..33 33 - - - 4759 RMVar_ID_4759 Human_SNP_ID_214793985 A-to-I Human chr4 - 175795487 175795487 175795487 CCTTGGCCACCGAAAATGTTGAGATTATAGGCATGAACCACCATGCCCAGCCCACAGTGCTTTTA CCTTGGCCACCGAAAATGTTGAGATTATAGGCTTGAACCACCATGCCCAGCCCACAGTGCTTTTA T A GPM6A Ensembl:ENSG00000150625 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1355486568 Functional Loss SNV dbSNP153 33..33 33 - - - 4760 RMVar_ID_4760 Human_SNP_ID_214794018 A-to-I Human chr4 - 175795628 175795627 175795628 TCCCACCTCTGCCTCCTCCCAGCTGGGACCACAGGTGTGTCCCACCATGCCCAGCTAACTTTTAA TCCCACCTCTGCCTCCTCCCAGCTGGGACCAC_GGTGTGTCCCACCATGCCCAGCTAACTTTTAA CT C GPM6A Ensembl:ENSG00000150625 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1006236752 Functional Loss DEL dbSNP153 33..33 33 - - - 4761 RMVar_ID_4761 Human_SNP_ID_214826841 A-to-I Human chr4 - 175931970 175931970 175931970 CTCCTGCCTGAGCTTCCAAAGTAGCTAGGACTACAGGCATGCACCACCATACCTGGCTAATTAAT CTCCTGCCTGAGCTTCCAAAGTAGCTAGGACTGCAGGCATGCACCACCATACCTGGCTAATTAAT T C GPM6A Ensembl:ENSG00000150625 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1172643498 Functional Loss SNV dbSNP153 33..33 33 - - - 4762 RMVar_ID_4762 Human_SNP_ID_214834731 A-to-I Human chr4 - 175964523 175964523 175964523 GAAGAAAGTGGCCATCTTCAAGCCAAGGAGAAAGAACTCAGAACAAACCAACCCTGCTGGCACTT GAAGAAAGTGGCCATCTTCAAGCCAAGGAGAAGGAACTCAGAACAAACCAACCCTGCTGGCACTT T C GPM6A Ensembl:ENSG00000150625 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs897780857 Functional Loss SNV dbSNP153 33..33 33 - - - 4763 RMVar_ID_4763 Human_SNP_ID_214927403 A-to-I Human chr4 + 176331183 176331183 176331183 GATGAAAAGCTGGGCTTTTTCTCTAAGATGATAATCTTAAAGCCCAGCTATTAATTGATAATGAA GATGAAAAGCTGGGCTTTTTCTCTAAGATGATCATCTTAAAGCCCAGCTATTAATTGATAATGAA A C SPCS3 Ensembl:ENSG00000129128 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1318770544 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_617287,Human_RBP_ID_22458064,Human_RBP_ID_25792258 RMVar_hsa_circ_85636,RMVar_hsa_circ_108404,RMVar_hsa_circ_100028,RMVar_hsa_circ_229639,RMVar_hsa_circ_229640,RMVar_hsa_circ_229641 4764 RMVar_ID_4764 Human_SNP_ID_214927513 A-to-I Human chr4 + 176331637 176331637 176331637 CTGAGACGGAGATCTGCTCTTACGCCCAGGCTAGAGTGAAGTGGCGCGATCTTGGCTTACTGCAA CTGAGACGGAGATCTGCTCTTACGCCCAGGCTGGAGTGAAGTGGCGCGATCTTGGCTTACTGCAA A G SPCS3 Ensembl:ENSG00000129128 Protein coding 3'UTR GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 29129909,30559470 RNA-Seq:(High) rs918818278 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_617301,Human_RBP_ID_8212101,Human_RBP_ID_15100004,Human_RBP_ID_24430799 Human_miRNA_ID_113120,Human_miRNA_ID_1968290 RMVar_hsa_circ_85636,RMVar_hsa_circ_108404,RMVar_hsa_circ_100028,RMVar_hsa_circ_229639,RMVar_hsa_circ_229640,RMVar_hsa_circ_229641 4765 RMVar_ID_4765 Human_SNP_ID_214927528 A-to-I Human chr4 + 176331682 176331682 176331682 GCGATCTTGGCTTACTGCAACCTCCACCCCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCGG GCGATCTTGGCTTACTGCAACCTCCACCCCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCGG A G SPCS3 Ensembl:ENSG00000129128 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1292261320 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_617302 Human_miRNA_ID_2723343 RMVar_hsa_circ_85636,RMVar_hsa_circ_108404,RMVar_hsa_circ_100028,RMVar_hsa_circ_229639,RMVar_hsa_circ_229640,RMVar_hsa_circ_229641 4766 RMVar_ID_4766 Human_SNP_ID_215181264 A-to-I Human chr4 + 177363850 177363850 177363850 TTGGCTCACTGCAGCCTCAACCTGTCGGACTCAAGCGATCCCCTAGCCTCAGCCTCCCAAGTAGC TTGGCTCACTGCAGCCTCAACCTGTCGGACTCCAGCGATCCCCTAGCCTCAGCCTCCCAAGTAGC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1024031567 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15103176 4767 RMVar_ID_4767 Human_SNP_ID_215181265 A-to-I Human chr4 + 177363850 177363850 177363850 TTGGCTCACTGCAGCCTCAACCTGTCGGACTCAAGCGATCCCCTAGCCTCAGCCTCCCAAGTAGC TTGGCTCACTGCAGCCTCAACCTGTCGGACTCTAGCGATCCCCTAGCCTCAGCCTCCCAAGTAGC A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1024031567 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15103176 4768 RMVar_ID_4768 Human_SNP_ID_391524019 A-to-I Human chr9 - 15303433 15303433 15303433 CTAGGAGGTTGAGGCTGCAGTGAACTCTGATCATGCCACTGCACTCCAGCCTGGGTGACAGACCC CTAGGAGGTTGAGGCTGCAGTGAACTCTGATCCTGCCACTGCACTCCAGCCTGGGTGACAGACCC T G TTC39B Ensembl:ENSG00000155158 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1044487099 Functional Loss SNV dbSNP153 33..33 33 - - - 4769 RMVar_ID_4769 Human_SNP_ID_391567097 A-to-I Human chr9 + 15435647 15435645 15435647 CAGCTACTCTGGAGGCTGGCAGGACAATCACTAGAACCCAGGAGGTGGAGGTTGCAGCGAGCCCA CAGCTACTCTGGAGGCTGGCAGGACAATCAC__GAACCCAGGAGGTGGAGGTTGCAGCGAGCCCA CTA C SNAPC3 Ensembl:ENSG00000164975 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1274484244 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_53117,RMVar_hsa_circ_352234,RMVar_hsa_circ_353051,RMVar_hsa_circ_347769,RMVar_hsa_circ_350739,RMVar_hsa_circ_105679,RMVar_hsa_circ_255814,RMVar_hsa_circ_20695,RMVar_hsa_circ_49560,RMVar_hsa_circ_255815,RMVar_hsa_circ_255813 4770 RMVar_ID_4770 Human_SNP_ID_391568710 A-to-I Human chr9 + 15440786 15440786 15440786 CCTGGCTAACACAGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTAGCTGGGCGCGGTGGCG CCTGGCTAACACAGTGAAACCCCGTCTCTACTGAAAATACAAAAAATTAGCTGGGCGCGGTGGCG A G SNAPC3 Ensembl:ENSG00000164975 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1190712247 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_183481 RMVar_hsa_circ_53117,RMVar_hsa_circ_352234,RMVar_hsa_circ_353051,RMVar_hsa_circ_347769,RMVar_hsa_circ_350739,RMVar_hsa_circ_105679,RMVar_hsa_circ_255814,RMVar_hsa_circ_20695,RMVar_hsa_circ_49560,RMVar_hsa_circ_255815,RMVar_hsa_circ_255813 4771 RMVar_ID_4771 Human_SNP_ID_391568711 A-to-I Human chr9 + 15440792 15440792 15440792 TAACACAGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTAGCTGGGCGCGGTGGCGAGTGTC TAACACAGTGAAACCCCGTCTCTACTAAAAATCCAAAAAATTAGCTGGGCGCGGTGGCGAGTGTC A C SNAPC3 Ensembl:ENSG00000164975 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1374610123 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_183481 RMVar_hsa_circ_53117,RMVar_hsa_circ_352234,RMVar_hsa_circ_353051,RMVar_hsa_circ_347769,RMVar_hsa_circ_350739,RMVar_hsa_circ_105679,RMVar_hsa_circ_255814,RMVar_hsa_circ_20695,RMVar_hsa_circ_49560,RMVar_hsa_circ_255815,RMVar_hsa_circ_255813 4772 RMVar_ID_4772 Human_SNP_ID_391568712 A-to-I Human chr9 + 15440792 15440792 15440792 TAACACAGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTAGCTGGGCGCGGTGGCGAGTGTC TAACACAGTGAAACCCCGTCTCTACTAAAAATGCAAAAAATTAGCTGGGCGCGGTGGCGAGTGTC A G SNAPC3 Ensembl:ENSG00000164975 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1374610123 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_183481 RMVar_hsa_circ_53117,RMVar_hsa_circ_352234,RMVar_hsa_circ_353051,RMVar_hsa_circ_347769,RMVar_hsa_circ_350739,RMVar_hsa_circ_105679,RMVar_hsa_circ_255814,RMVar_hsa_circ_20695,RMVar_hsa_circ_49560,RMVar_hsa_circ_255815,RMVar_hsa_circ_255813 4773 RMVar_ID_4773 Human_SNP_ID_391573629 A-to-I Human chr9 + 15454769 15454769 15454769 ACCATGCTGGCTAACACAGTGAAAGCGTCTCTACTAAAAATACAAAAATTAGCCAGGCGTGGTGG ACCATGCTGGCTAACACAGTGAAAGCGTCTCTTCTAAAAATACAAAAATTAGCCAGGCGTGGTGG A T SNAPC3 Ensembl:ENSG00000164975 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs939373397 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3627,RMVar_hsa_circ_53117,RMVar_hsa_circ_347769,RMVar_hsa_circ_105679,RMVar_hsa_circ_255814,RMVar_hsa_circ_20695,RMVar_hsa_circ_49560,RMVar_hsa_circ_255815,RMVar_hsa_circ_89552,RMVar_hsa_circ_289254,RMVar_hsa_circ_255816,RMVar_hsa_circ_310992,RMVar_hsa_circ_12268,RMVar_hsa_circ_255818,RMVar_hsa_circ_73144,RMVar_hsa_circ_350431 4774 RMVar_ID_4774 Human_SNP_ID_391574454 A-to-I Human chr9 + 15457348 15457348 15457348 CAGGTGTCGTGGCTCACAGCTGTAATCCCAGCACCTTGGGAGGCTGAGGTGGGAGGATCGCTTGA CAGGTGTCGTGGCTCACAGCTGTAATCCCAGCCCCTTGGGAGGCTGAGGTGGGAGGATCGCTTGA A C SNAPC3 Ensembl:ENSG00000164975 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1194306867 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3627,RMVar_hsa_circ_53117,RMVar_hsa_circ_347769,RMVar_hsa_circ_105679,RMVar_hsa_circ_255814,RMVar_hsa_circ_20695,RMVar_hsa_circ_49560,RMVar_hsa_circ_255815,RMVar_hsa_circ_89552,RMVar_hsa_circ_289254,RMVar_hsa_circ_255816,RMVar_hsa_circ_310992,RMVar_hsa_circ_12268,RMVar_hsa_circ_255818,RMVar_hsa_circ_73144,RMVar_hsa_circ_350431 4775 RMVar_ID_4775 Human_SNP_ID_391575341 A-to-I Human chr9 + 15460069 15460069 15460069 TTTATAACATAGTTTAATTTTATATTTATTCCAGATAGTATTTAATTTAGTGCTTTTTACCCATT TTTATAACATAGTTTAATTTTATATTTATTCCCGATAGTATTTAATTTAGTGCTTTTTACCCATT A C SNAPC3 Ensembl:ENSG00000164975 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1303445712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_91599,Human_RBP_ID_7911015,Human_RBP_ID_24443344,Human_RBP_ID_26213739 Human_miRNA_ID_1549198 RMVar_hsa_circ_3627,RMVar_hsa_circ_347769,RMVar_hsa_circ_105679,RMVar_hsa_circ_255814,RMVar_hsa_circ_20695,RMVar_hsa_circ_49560,RMVar_hsa_circ_255815,RMVar_hsa_circ_89552,RMVar_hsa_circ_289254,RMVar_hsa_circ_255816,RMVar_hsa_circ_12268,RMVar_hsa_circ_76337,RMVar_hsa_circ_276049,RMVar_hsa_circ_73144,RMVar_hsa_circ_265336,RMVar_hsa_circ_255819,RMVar_hsa_circ_255820,RMVar_hsa_circ_118699,RMVar_hsa_circ_255821 4776 RMVar_ID_4776 Human_SNP_ID_391575475 A-to-I Human chr9 + 15460508 15460508 15460508 CGCCTCCCGGATTCAAGTGATTCTCCTGCCACAGCCTCCTGAGTAGCTGGGATTGCAGGCACCTG CGCCTCCCGGATTCAAGTGATTCTCCTGCCACGGCCTCCTGAGTAGCTGGGATTGCAGGCACCTG A G SNAPC3 Ensembl:ENSG00000164975 Protein coding 3'UTR GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1033169534 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3627,RMVar_hsa_circ_347769,RMVar_hsa_circ_105679,RMVar_hsa_circ_255814,RMVar_hsa_circ_49560,RMVar_hsa_circ_255815,RMVar_hsa_circ_89552,RMVar_hsa_circ_255816,RMVar_hsa_circ_76337,RMVar_hsa_circ_73144,RMVar_hsa_circ_265336,RMVar_hsa_circ_255820,RMVar_hsa_circ_118699,RMVar_hsa_circ_255821 4777 RMVar_ID_4777 Human_SNP_ID_391575478 A-to-I Human chr9 + 15460520 15460520 15460520 TCAAGTGATTCTCCTGCCACAGCCTCCTGAGTAGCTGGGATTGCAGGCACCTGGCACCATGCCTG TCAAGTGATTCTCCTGCCACAGCCTCCTGAGTGGCTGGGATTGCAGGCACCTGGCACCATGCCTG A G SNAPC3 Ensembl:ENSG00000164975 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1224065063 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3627,RMVar_hsa_circ_347769,RMVar_hsa_circ_105679,RMVar_hsa_circ_255814,RMVar_hsa_circ_49560,RMVar_hsa_circ_255815,RMVar_hsa_circ_89552,RMVar_hsa_circ_255816,RMVar_hsa_circ_76337,RMVar_hsa_circ_73144,RMVar_hsa_circ_265336,RMVar_hsa_circ_255820,RMVar_hsa_circ_118699,RMVar_hsa_circ_255821 4778 RMVar_ID_4778 Human_SNP_ID_391575891 A-to-I Human chr9 - 15461679 15461679 15461679 TATAGGTTTCGTCAGTTTTCCATGTGTAAGATAAATGTCTGTTCTTAGCCATCCAGATATTCAGT TATAGGTTTCGTCAGTTTTCCATGTGTAAGATCAATGTCTGTTCTTAGCCATCCAGATATTCAGT T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432712759 Functional Loss SNV dbSNP153 33..33 33 - - - 4779 RMVar_ID_4779 Human_SNP_ID_391576763 A-to-I Human chr9 - 15464105 15464105 15464105 CTTAGATTTATTCTAGTTAAGCCATAAGTTCAACGTGTAAACTTGTTTTCATTAAAGAATTTTTC CTTAGATTTATTCTAGTTAAGCCATAAGTTCAGCGTGTAAACTTGTTTTCATTAAAGAATTTTTC T C PSIP1 Ensembl:ENSG00000164985 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348307558 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1704034,Human_RBP_ID_18397412,Human_RBP_ID_22518142,Human_RBP_ID_26737280 RMVar_hsa_circ_98452,RMVar_hsa_circ_124498,RMVar_hsa_circ_114356,RMVar_hsa_circ_255823,RMVar_hsa_circ_255825,RMVar_hsa_circ_87910,RMVar_hsa_circ_255824,RMVar_hsa_circ_255822 4780 RMVar_ID_4780 Human_SNP_ID_391577512 A-to-I Human chr9 + 15466213 15466213 15466213 CGGGCTGGCCAACATGGTGAAACCTCATCTCTACTAAAAATACAAAAAATTAGATGGGCGTGGTG CGGGCTGGCCAACATGGTGAAACCTCATCTCTGCTAAAAATACAAAAAATTAGATGGGCGTGGTG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1182441400 Functional Loss SNV dbSNP153 33..33 33 - - - 4781 RMVar_ID_4781 Human_SNP_ID_391590191 A-to-I Human chr9 - 15504018 15504018 15504018 TTTTTGGGCTGGGCGCGGTGGCTTACGCGTGTAATCCCAGCACTTTGGGAGGCTGAAGCGGGCGG TTTTTGGGCTGGGCGCGGTGGCTTACGCGTGTGATCCCAGCACTTTGGGAGGCTGAAGCGGGCGG T C PSIP1 Ensembl:ENSG00000164985 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1031115367 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16629606 RMVar_hsa_circ_313857 4782 RMVar_ID_4782 Human_SNP_ID_391590641 A-to-I Human chr9 - 15505187 15505187 15505187 GACACCTGTAATCCCAACACTTTGGGAGGCCAAGGCGGGAGGGTCACTTGAGTTCAGGAGTTGGA GACACCTGTAATCCCAACACTTTGGGAGGCCAGGGCGGGAGGGTCACTTGAGTTCAGGAGTTGGA T C PSIP1 Ensembl:ENSG00000164985 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs777481878 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_313857 4783 RMVar_ID_4783 Human_SNP_ID_391590647 A-to-I Human chr9 - 15505203 15505203 15505203 GCTGGGTGTGGTGGCTGACACCTGTAATCCCAACACTTTGGGAGGCCAAGGCGGGAGGGTCACTT GCTGGGTGTGGTGGCTGACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGAGGGTCACTT T C PSIP1 Ensembl:ENSG00000164985 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1158580627 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_313857 4784 RMVar_ID_4784 Human_SNP_ID_391647035 A-to-I Human chr9 + 15663880 15663880 15663880 CGCCTGCCTCGGCCTCCCAAAGTGCCGGGATTACATGCGTGAGCCACCGCGCCCGGCTGAGAATT CGCCTGCCTCGGCCTCCCAAAGTGCCGGGATTGCATGCGTGAGCCACCGCGCCCGGCTGAGAATT A G CCDC171 Ensembl:ENSG00000164989 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs954689133 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_31694,RMVar_hsa_circ_62696,RMVar_hsa_circ_33507,RMVar_hsa_circ_7382,RMVar_hsa_circ_69548,RMVar_hsa_circ_10791,RMVar_hsa_circ_26820,RMVar_hsa_circ_30402,RMVar_hsa_circ_333184,RMVar_hsa_circ_361445,RMVar_hsa_circ_328539,RMVar_hsa_circ_255835,RMVar_hsa_circ_319294,RMVar_hsa_circ_344864,RMVar_hsa_circ_112941,RMVar_hsa_circ_255834 4785 RMVar_ID_4785 Human_SNP_ID_391889171 A-to-I Human chr9 - 16463835 16463835 16463835 TGCCTTGGCCTCCCGAAGTGCTGGGATTACAGACATGAGCCACCGGGCCTCCCAAAGTGCTGGGA TGCCTTGGCCTCCCGAAGTGCTGGGATTACAGTCATGAGCCACCGGGCCTCCCAAAGTGCTGGGA T A BNC2 Ensembl:ENSG00000173068 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1229924339 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19642,RMVar_hsa_circ_331231 4786 RMVar_ID_4786 Human_SNP_ID_391900877 A-to-I Human chr9 - 16502248 16502248 16502248 GAACTGAATTCAAGTGATCCTTCCAAGTAGCTAGCACTACAGATGTGTGCCATCACGTCTGGCTA GAACTGAATTCAAGTGATCCTTCCAAGTAGCTCGCACTACAGATGTGTGCCATCACGTCTGGCTA T G BNC2 Ensembl:ENSG00000173068 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042137102 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19642,RMVar_hsa_circ_331231 4787 RMVar_ID_4787 Human_SNP_ID_391947015 A-to-I Human chr9 - 16662556 16662556 16662556 AATTTTTGTATGTTTAGTGGAGACGAGGTTTCACCATATTGGCCAGGCTGGCCTTGAACTCTTGA AATTTTTGTATGTTTAGTGGAGACGAGGTTTCCCCATATTGGCCAGGCTGGCCTTGAACTCTTGA T G BNC2 Ensembl:ENSG00000173068 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs778224034 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_290021,RMVar_hsa_circ_298080,RMVar_hsa_circ_255850,RMVar_hsa_circ_346576,RMVar_hsa_circ_359137,RMVar_hsa_circ_255851 4788 RMVar_ID_4788 Human_SNP_ID_391947038 A-to-I Human chr9 - 16662624 16662624 16662624 TTAAATGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGAGACTACAGGCATGCACCACCATGTTCA TTAAATGATTCTCCTGCCTCAGCCTCCTGAGTGGCTGAGACTACAGGCATGCACCACCATGTTCA T C BNC2 Ensembl:ENSG00000173068 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs567168223 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_290021,RMVar_hsa_circ_298080,RMVar_hsa_circ_255850,RMVar_hsa_circ_346576,RMVar_hsa_circ_359137,RMVar_hsa_circ_255851 4789 RMVar_ID_4789 Human_SNP_ID_392005882 A-to-I Human chr9 - 16849470 16849470 16849470 CCTGTAATCTCAGCTACTTTGGGGGCTGAGGCAGGAGACTTGCTTGAACTTGGGAGGTGGAGGTT CCTGTAATCTCAGCTACTTTGGGGGCTGAGGCGGGAGACTTGCTTGAACTTGGGAGGTGGAGGTT T C BNC2 Ensembl:ENSG00000173068 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs999887487 Functional Loss SNV dbSNP153 33..33 33 - - - 4790 RMVar_ID_4790 Human_SNP_ID_392059458 A-to-I Human chr9 - 17001215 17001215 17001215 TTACCAGGATGGTTGCATGGAAGTCAGAATCCACTAAGGAGTGTGGAAGAACTCACCTGCCAAAT TTACCAGGATGGTTGCATGGAAGTCAGAATCCTCTAAGGAGTGTGGAAGAACTCACCTGCCAAAT T A RF02543-052,RF00017-4567 RNACentral:URS0000973FF9,RNACentral:URS000093B3AD rRNA,SRP RNA exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1271987789 Functional Loss SNV dbSNP153 33..33 33 - - - 4791 RMVar_ID_4791 Human_SNP_ID_392059459 A-to-I Human chr9 - 17001215 17001215 17001215 TTACCAGGATGGTTGCATGGAAGTCAGAATCCACTAAGGAGTGTGGAAGAACTCACCTGCCAAAT TTACCAGGATGGTTGCATGGAAGTCAGAATCCGCTAAGGAGTGTGGAAGAACTCACCTGCCAAAT T C RF02543-052,RF00017-4567 RNACentral:URS0000973FF9,RNACentral:URS000093B3AD rRNA,SRP RNA exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1271987789 Functional Loss SNV dbSNP153 33..33 33 - - - 4792 RMVar_ID_4792 Human_SNP_ID_392107418 A-to-I Human chr9 + 17164935 17164935 17164935 TTGGCTCACTGCGACCTCTGCCACCCGAGTTCAAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGC TTGGCTCACTGCGACCTCTGCCACCCGAGTTCCAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGC A C CNTLN Ensembl:ENSG00000044459 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs370715481 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70856,RMVar_hsa_circ_366610 4793 RMVar_ID_4793 Human_SNP_ID_392163926 A-to-I Human chr9 + 17346058 17346058 17346058 AGTATAAAGAAATACACAAAACTGGATAATTTATAAAGGAAAGAGATTTAATTGACTCACAGTTC AGTATAAAGAAATACACAAAACTGGATAATTTGTAAAGGAAAGAGATTTAATTGACTCACAGTTC A G CNTLN Ensembl:ENSG00000044459 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1162409429 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_326214,RMVar_hsa_circ_54759,RMVar_hsa_circ_255866,RMVar_hsa_circ_60147,RMVar_hsa_circ_369230,RMVar_hsa_circ_290010,RMVar_hsa_circ_334545,RMVar_hsa_circ_366183,RMVar_hsa_circ_317613,RMVar_hsa_circ_280721,RMVar_hsa_circ_57426,RMVar_hsa_circ_255868,RMVar_hsa_circ_46930,RMVar_hsa_circ_255867,RMVar_hsa_circ_30626,RMVar_hsa_circ_255871,RMVar_hsa_circ_286558,RMVar_hsa_circ_362002,RMVar_hsa_circ_368693,RMVar_hsa_circ_364157,RMVar_hsa_circ_304159,RMVar_hsa_circ_29553,RMVar_hsa_circ_255873,RMVar_hsa_circ_316356,RMVar_hsa_circ_347071,RMVar_hsa_circ_351144,RMVar_hsa_circ_255875 4794 RMVar_ID_4794 Human_SNP_ID_392163927 A-to-I Human chr9 + 17346066 17346063 17346067 GAAATACACAAAACTGGATAATTTATAAAGGAAAGAGATTTAATTGACTCACAGTTCCACACGGC GAAATACACAAAACTGGATAATTTATAAAG____GAGATTTAATTGACTCACAGTTCCACACGGC GGAAA G CNTLN Ensembl:ENSG00000044459 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1417987432 Functional Loss DEL dbSNP153 31..34 33 - - - RMVar_hsa_circ_326214,RMVar_hsa_circ_54759,RMVar_hsa_circ_255866,RMVar_hsa_circ_60147,RMVar_hsa_circ_369230,RMVar_hsa_circ_290010,RMVar_hsa_circ_334545,RMVar_hsa_circ_366183,RMVar_hsa_circ_317613,RMVar_hsa_circ_280721,RMVar_hsa_circ_57426,RMVar_hsa_circ_255868,RMVar_hsa_circ_46930,RMVar_hsa_circ_255867,RMVar_hsa_circ_30626,RMVar_hsa_circ_255871,RMVar_hsa_circ_286558,RMVar_hsa_circ_362002,RMVar_hsa_circ_368693,RMVar_hsa_circ_364157,RMVar_hsa_circ_304159,RMVar_hsa_circ_29553,RMVar_hsa_circ_255873,RMVar_hsa_circ_316356,RMVar_hsa_circ_347071,RMVar_hsa_circ_351144,RMVar_hsa_circ_255875 4795 RMVar_ID_4795 Human_SNP_ID_392179126 A-to-I Human chr9 + 17396170 17396170 17396170 TGAATAATACACCCCTAGTTTAGCATATCGTCAAGAAATAACCATAAAAATGGGCAACCAGCACC TGAATAATACACCCCTAGTTTAGCATATCGTCCAGAAATAACCATAAAAATGGGCAACCAGCACC A C CNTLN Ensembl:ENSG00000044459 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs374786652 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_326214,RMVar_hsa_circ_54759,RMVar_hsa_circ_369230,RMVar_hsa_circ_290010,RMVar_hsa_circ_366183,RMVar_hsa_circ_317613,RMVar_hsa_circ_57426,RMVar_hsa_circ_255868,RMVar_hsa_circ_30626,RMVar_hsa_circ_255871,RMVar_hsa_circ_286558,RMVar_hsa_circ_362002,RMVar_hsa_circ_364157,RMVar_hsa_circ_29553,RMVar_hsa_circ_255873,RMVar_hsa_circ_351144,RMVar_hsa_circ_3251,RMVar_hsa_circ_290540,RMVar_hsa_circ_255876,RMVar_hsa_circ_255875,RMVar_hsa_circ_319920,RMVar_hsa_circ_356507,RMVar_hsa_circ_255877,RMVar_hsa_circ_366846,RMVar_hsa_circ_58139,RMVar_hsa_circ_55671,RMVar_hsa_circ_9034,RMVar_hsa_circ_255879,RMVar_hsa_circ_17185 4796 RMVar_ID_4796 Human_SNP_ID_392235540 A-to-I Human chr9 + 17584396 17584396 17584396 GAGGTGGCAGGTGCCTGTAATCCCACCTACCCAGGAGGCTGAGGCAGGAGAATTGCCTGAACCCA GAGGTGGCAGGTGCCTGTAATCCCACCTACCCCGGAGGCTGAGGCAGGAGAATTGCCTGAACCCA A C SH3GL2 Ensembl:ENSG00000107295 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1320234438 Functional Loss SNV dbSNP153 33..33 33 - - - 4797 RMVar_ID_4797 Human_SNP_ID_392237419 A-to-I Human chr9 + 17590783 17590778 17590783 TCACAAAGGTGTATTTAATTCATTTTTGTTTTATTTTGTTTTTGAGACAGGGTCTCACTCTGTCG TCACAAAGGTGTATTTAATTCATTTTTG_____TTTTGTTTTTGAGACAGGGTCTCACTCTGTCG GTTTTA G SH3GL2 Ensembl:ENSG00000107295 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs764203903 Functional Loss DEL dbSNP153 29..33 33 - - - Human_RBP_ID_7912625,Human_RBP_ID_16631674 4798 RMVar_ID_4798 Human_SNP_ID_392237420 A-to-I Human chr9 + 17590783 17590783 17590783 TCACAAAGGTGTATTTAATTCATTTTTGTTTTATTTTGTTTTTGAGACAGGGTCTCACTCTGTCG TCACAAAGGTGTATTTAATTCATTTTTGTTTTGTTTTGTTTTTGAGACAGGGTCTCACTCTGTCG A G SH3GL2 Ensembl:ENSG00000107295 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1269830385 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7912625,Human_RBP_ID_16631674 4799 RMVar_ID_4799 Human_SNP_ID_392245097 A-to-I Human chr9 + 17615534 17615534 17615534 AAAATTAGCCAGGCGTGGCAGCGGGCGCCTGTAATCCCAGCTACTCGGGAAGCTGAGGCAGGAGA AAAATTAGCCAGGCGTGGCAGCGGGCGCCTGTTATCCCAGCTACTCGGGAAGCTGAGGCAGGAGA A T SH3GL2 Ensembl:ENSG00000107295 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs914554604 Functional Loss SNV dbSNP153 33..33 33 - - - 4800 RMVar_ID_4800 Human_SNP_ID_392275905 A-to-I Human chr9 + 17710278 17710278 17710278 GATGTGTTTGCATCCCTTTCTGTCATGACTGTAAGTTTCCTGAGGCCTCCCCAGCCCTGCAGAAC GATGTGTTTGCATCCCTTTCTGTCATGACTGTGAGTTTCCTGAGGCCTCCCCAGCCCTGCAGAAC A G SH3GL2 Ensembl:ENSG00000107295 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1457319747 Functional Loss SNV dbSNP153 33..33 33 - - - 4801 RMVar_ID_4801 Human_SNP_ID_392675110 A-to-I Human chr9 + 19026916 19026916 19026916 AAAAGAAGATGGCAACCGTGTGGGATGAGGCCAAGCAAGATGGAACTGGGGTGGAGGTGCTCAAC AAAAGAAGATGGCAACCGTGTGGGATGAGGCCGAGCAAGATGGAACTGGGGTGGAGGTGCTCAAC A G AL356000.1 Ensembl:ENSG00000236680 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1434825963 Functional Loss SNV dbSNP153 33..33 33 - - - 4802 RMVar_ID_4802 Human_SNP_ID_392675224 A-to-I Human chr9 + 19027199 19027199 19027199 TCCAAATATTGACCTGGACTCCCAGAGGAAGGACAAGTGTGCTGTGATCAAAACCTCTACACGAC TCCAAATATTGACCTGGACTCCCAGAGGAAGGCCAAGTGTGCTGTGATCAAAACCTCTACACGAC A C AL356000.1 Ensembl:ENSG00000236680 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048831612 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1844410 4803 RMVar_ID_4803 Human_SNP_ID_392675225 A-to-I Human chr9 + 19027199 19027199 19027199 TCCAAATATTGACCTGGACTCCCAGAGGAAGGACAAGTGTGCTGTGATCAAAACCTCTACACGAC TCCAAATATTGACCTGGACTCCCAGAGGAAGGGCAAGTGTGCTGTGATCAAAACCTCTACACGAC A G AL356000.1 Ensembl:ENSG00000236680 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048831612 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1844410 4804 RMVar_ID_4804 Human_SNP_ID_392675238 A-to-I Human chr9 + 19027236 19027236 19027236 TGTGCTGTGATCAAAACCTCTACACGACAGACATACTTCCTACCTGTGATTGGATTGGTGGATGT TGTGCTGTGATCAAAACCTCTACACGACAGACGTACTTCCTACCTGTGATTGGATTGGTGGATGT A G AL356000.1 Ensembl:ENSG00000236680 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879007223 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8275781,Human_RBP_ID_18542260 Human_miRNA_ID_1886242,Human_miRNA_ID_1901563 4805 RMVar_ID_4805 Human_SNP_ID_392675243 A-to-I Human chr9 + 19027257 19027257 19027257 ACACGACAGACATACTTCCTACCTGTGATTGGATTGGTGGATGTTGAAAAGCTAAAGCCAGGAGA ACACGACAGACATACTTCCTACCTGTGATTGGGTTGGTGGATGTTGAAAAGCTAAAGCCAGGAGA A G AL356000.1 Ensembl:ENSG00000236680 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1477872927 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5023930 4806 RMVar_ID_4806 Human_SNP_ID_392687252 A-to-I Human chr9 - 19065584 19065584 19065584 CGCTTGCCTCAGCCTCCCAAAGTGGTGGGATTACAGGCGTGAGCCACCGCGCCCAGCCCAAAATT CGCTTGCCTCAGCCTCCCAAAGTGGTGGGATTCCAGGCGTGAGCCACCGCGCCCAGCCCAAAATT T G HAUS6 Ensembl:ENSG00000147874 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1040059283 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_65,RMVar_hsa_circ_255915,RMVar_hsa_circ_78693,RMVar_hsa_circ_45390,RMVar_hsa_circ_300056,RMVar_hsa_circ_13414,RMVar_hsa_circ_50374,RMVar_hsa_circ_23909,RMVar_hsa_circ_276710,RMVar_hsa_circ_314919,RMVar_hsa_circ_347801,RMVar_hsa_circ_286618,RMVar_hsa_circ_38223,RMVar_hsa_circ_255917,RMVar_hsa_circ_255918,RMVar_hsa_circ_265452,RMVar_hsa_circ_265284 4807 RMVar_ID_4807 Human_SNP_ID_392687268 A-to-I Human chr9 - 19065636 19065636 19065636 GGGTTTCATCATGTTGGCGAGGCTGGTCTTCAACTCCTGACCTCAGGTGATCCGCTTGCCTCAGC GGGTTTCATCATGTTGGCGAGGCTGGTCTTCACCTCCTGACCTCAGGTGATCCGCTTGCCTCAGC T G HAUS6 Ensembl:ENSG00000147874 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1030022540 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_65,RMVar_hsa_circ_255915,RMVar_hsa_circ_78693,RMVar_hsa_circ_45390,RMVar_hsa_circ_300056,RMVar_hsa_circ_13414,RMVar_hsa_circ_50374,RMVar_hsa_circ_23909,RMVar_hsa_circ_276710,RMVar_hsa_circ_314919,RMVar_hsa_circ_347801,RMVar_hsa_circ_286618,RMVar_hsa_circ_38223,RMVar_hsa_circ_255917,RMVar_hsa_circ_255918,RMVar_hsa_circ_265452,RMVar_hsa_circ_265284 4808 RMVar_ID_4808 Human_SNP_ID_392687318 A-to-I Human chr9 - 19065802 19065802 19065802 AGTTTCGTTCCTGTTGCCCAGGCTGGAGTGCAATGGCACGATCTCGGCTCACTGCAACTGCTGCC AGTTTCGTTCCTGTTGCCCAGGCTGGAGTGCAGTGGCACGATCTCGGCTCACTGCAACTGCTGCC T C HAUS6 Ensembl:ENSG00000147874 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1351638215 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_65,RMVar_hsa_circ_255915,RMVar_hsa_circ_78693,RMVar_hsa_circ_45390,RMVar_hsa_circ_300056,RMVar_hsa_circ_13414,RMVar_hsa_circ_50374,RMVar_hsa_circ_23909,RMVar_hsa_circ_276710,RMVar_hsa_circ_314919,RMVar_hsa_circ_347801,RMVar_hsa_circ_286618,RMVar_hsa_circ_38223,RMVar_hsa_circ_255917,RMVar_hsa_circ_255918,RMVar_hsa_circ_265452,RMVar_hsa_circ_265284 4809 RMVar_ID_4809 Human_SNP_ID_392688573 A-to-I Human chr9 - 19069899 19069899 19069899 AAAAGGTGTGGTCTTTCTGGGTTGCAGAGGCTAGTCTTTAACTCTTGGCCTCAAGTGATCCTCCT AAAAGGTGTGGTCTTTCTGGGTTGCAGAGGCTGGTCTTTAACTCTTGGCCTCAAGTGATCCTCCT T C HAUS6 Ensembl:ENSG00000147874 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs999209101 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_65,RMVar_hsa_circ_255915,RMVar_hsa_circ_78693,RMVar_hsa_circ_45390,RMVar_hsa_circ_300056,RMVar_hsa_circ_13414,RMVar_hsa_circ_50374,RMVar_hsa_circ_23909,RMVar_hsa_circ_276710,RMVar_hsa_circ_314919,RMVar_hsa_circ_347801,RMVar_hsa_circ_286618,RMVar_hsa_circ_38223,RMVar_hsa_circ_255917,RMVar_hsa_circ_255918,RMVar_hsa_circ_265452,RMVar_hsa_circ_265284 4810 RMVar_ID_4810 Human_SNP_ID_392689202 A-to-I Human chr9 - 19072033 19072033 19072033 GGCATGTGCCACCATGCCCAGCTGATTTTTGTATTTTTAGTAGAGACGGGGCCAGGCTGGTCTCA GGCATGTGCCACCATGCCCAGCTGATTTTTGTGTTTTTAGTAGAGACGGGGCCAGGCTGGTCTCA T C HAUS6 Ensembl:ENSG00000147874 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs929230652 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_65,RMVar_hsa_circ_255915,RMVar_hsa_circ_78693,RMVar_hsa_circ_45390,RMVar_hsa_circ_300056,RMVar_hsa_circ_13414,RMVar_hsa_circ_50374,RMVar_hsa_circ_23909,RMVar_hsa_circ_276710,RMVar_hsa_circ_314919,RMVar_hsa_circ_286618,RMVar_hsa_circ_38223,RMVar_hsa_circ_255917,RMVar_hsa_circ_255918,RMVar_hsa_circ_265284,RMVar_hsa_circ_255920,RMVar_hsa_circ_112509,RMVar_hsa_circ_284016,RMVar_hsa_circ_328767,RMVar_hsa_circ_333058,RMVar_hsa_circ_347154,RMVar_hsa_circ_305585,RMVar_hsa_circ_281086,RMVar_hsa_circ_255922,RMVar_hsa_circ_255923,RMVar_hsa_circ_255921,RMVar_hsa_circ_255919 4811 RMVar_ID_4811 Human_SNP_ID_392689948 A-to-I Human chr9 - 19074410 19074410 19074410 AAAATTAGCCAGGCCTGGTGGTGTGTGTCTGTAGTCCTAGCTATTCAGGAGGCTGAGGCAGGAGA AAAATTAGCCAGGCCTGGTGGTGTGTGTCTGTGGTCCTAGCTATTCAGGAGGCTGAGGCAGGAGA T C HAUS6 Ensembl:ENSG00000147874 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1445016071 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_65,RMVar_hsa_circ_255915,RMVar_hsa_circ_78693,RMVar_hsa_circ_45390,RMVar_hsa_circ_300056,RMVar_hsa_circ_13414,RMVar_hsa_circ_50374,RMVar_hsa_circ_23909,RMVar_hsa_circ_276710,RMVar_hsa_circ_314919,RMVar_hsa_circ_286618,RMVar_hsa_circ_38223,RMVar_hsa_circ_255917,RMVar_hsa_circ_255918,RMVar_hsa_circ_265284,RMVar_hsa_circ_255920,RMVar_hsa_circ_112509,RMVar_hsa_circ_284016,RMVar_hsa_circ_328767,RMVar_hsa_circ_333058,RMVar_hsa_circ_347154,RMVar_hsa_circ_305585,RMVar_hsa_circ_281086,RMVar_hsa_circ_255922,RMVar_hsa_circ_255923,RMVar_hsa_circ_255921,RMVar_hsa_circ_255919 4812 RMVar_ID_4812 Human_SNP_ID_392689996 A-to-I Human chr9 - 19074547 19074547 19074547 CTGCATAGGGCTGGGCATAGCAGCTCACACCTATAATCCTGGCACTTTGGGAAGCCTAGGGTGGA CTGCATAGGGCTGGGCATAGCAGCTCACACCTGTAATCCTGGCACTTTGGGAAGCCTAGGGTGGA T C HAUS6 Ensembl:ENSG00000147874 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs139255517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26215056 RMVar_hsa_circ_65,RMVar_hsa_circ_255915,RMVar_hsa_circ_78693,RMVar_hsa_circ_45390,RMVar_hsa_circ_300056,RMVar_hsa_circ_13414,RMVar_hsa_circ_50374,RMVar_hsa_circ_23909,RMVar_hsa_circ_276710,RMVar_hsa_circ_314919,RMVar_hsa_circ_286618,RMVar_hsa_circ_38223,RMVar_hsa_circ_255917,RMVar_hsa_circ_255918,RMVar_hsa_circ_265284,RMVar_hsa_circ_255920,RMVar_hsa_circ_112509,RMVar_hsa_circ_284016,RMVar_hsa_circ_328767,RMVar_hsa_circ_333058,RMVar_hsa_circ_347154,RMVar_hsa_circ_305585,RMVar_hsa_circ_281086,RMVar_hsa_circ_255922,RMVar_hsa_circ_255923,RMVar_hsa_circ_255921,RMVar_hsa_circ_255919 4813 RMVar_ID_4813 Human_SNP_ID_392692559 A-to-I Human chr9 - 19081846 19081846 19081846 TGGCCAGGCCGGCTTAGAGCTCCTGACCTCAAATGATCCTCTTGCCTCGGCCCCCAAAGTGCTGG TGGCCAGGCCGGCTTAGAGCTCCTGACCTCAAGTGATCCTCTTGCCTCGGCCCCCAAAGTGCTGG T C HAUS6 Ensembl:ENSG00000147874 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1213089877 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_255915,RMVar_hsa_circ_78693,RMVar_hsa_circ_45390,RMVar_hsa_circ_300056,RMVar_hsa_circ_13414,RMVar_hsa_circ_10785,RMVar_hsa_circ_50374,RMVar_hsa_circ_23909,RMVar_hsa_circ_314919,RMVar_hsa_circ_286618,RMVar_hsa_circ_38223,RMVar_hsa_circ_255918,RMVar_hsa_circ_265284,RMVar_hsa_circ_255920,RMVar_hsa_circ_112509,RMVar_hsa_circ_284016,RMVar_hsa_circ_328767,RMVar_hsa_circ_333058,RMVar_hsa_circ_305585,RMVar_hsa_circ_255922,RMVar_hsa_circ_255923,RMVar_hsa_circ_255921,RMVar_hsa_circ_319550,RMVar_hsa_circ_282415,RMVar_hsa_circ_32033,RMVar_hsa_circ_311005,RMVar_hsa_circ_255924,RMVar_hsa_circ_7210,RMVar_hsa_circ_342562,RMVar_hsa_circ_352497,RMVar_hsa_circ_331894,RMVar_hsa_circ_255925,RMVar_hsa_circ_275458,RMVar_hsa_circ_355702,RMVar_hsa_circ_266838 4814 RMVar_ID_4814 Human_SNP_ID_392692581 A-to-I Human chr9 - 19081899 19081897 19081900 TGTGACTCTCTGAAGAGAGACACTTCTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCCGG TGTGACTCTCTGAAGAGAGACACTTCTTTAG___AGACGGGGTTTCACCATGTTGGCCAGGCCGG TCTA T HAUS6 Ensembl:ENSG00000147874 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs200814609 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_255915,RMVar_hsa_circ_78693,RMVar_hsa_circ_45390,RMVar_hsa_circ_300056,RMVar_hsa_circ_13414,RMVar_hsa_circ_10785,RMVar_hsa_circ_50374,RMVar_hsa_circ_23909,RMVar_hsa_circ_314919,RMVar_hsa_circ_286618,RMVar_hsa_circ_38223,RMVar_hsa_circ_255918,RMVar_hsa_circ_265284,RMVar_hsa_circ_255920,RMVar_hsa_circ_112509,RMVar_hsa_circ_284016,RMVar_hsa_circ_328767,RMVar_hsa_circ_333058,RMVar_hsa_circ_305585,RMVar_hsa_circ_255922,RMVar_hsa_circ_255923,RMVar_hsa_circ_255921,RMVar_hsa_circ_319550,RMVar_hsa_circ_282415,RMVar_hsa_circ_32033,RMVar_hsa_circ_311005,RMVar_hsa_circ_255924,RMVar_hsa_circ_7210,RMVar_hsa_circ_342562,RMVar_hsa_circ_352497,RMVar_hsa_circ_331894,RMVar_hsa_circ_255925,RMVar_hsa_circ_275458,RMVar_hsa_circ_355702,RMVar_hsa_circ_266838 4815 RMVar_ID_4815 Human_SNP_ID_392694140 A-to-I Human chr9 - 19086404 19086404 19086404 GTTGGCCAGGCTGGTCTTGAACTCTTGAGCTCAGATGATCTGCATGCCTTGGCCTCCCAAAGTGC GTTGGCCAGGCTGGTCTTGAACTCTTGAGCTCGGATGATCTGCATGCCTTGGCCTCCCAAAGTGC T C HAUS6 Ensembl:ENSG00000147874 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1049672269 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16632412 RMVar_hsa_circ_255915,RMVar_hsa_circ_78693,RMVar_hsa_circ_45390,RMVar_hsa_circ_300056,RMVar_hsa_circ_13414,RMVar_hsa_circ_50374,RMVar_hsa_circ_23909,RMVar_hsa_circ_314919,RMVar_hsa_circ_286618,RMVar_hsa_circ_38223,RMVar_hsa_circ_255918,RMVar_hsa_circ_255920,RMVar_hsa_circ_112509,RMVar_hsa_circ_284016,RMVar_hsa_circ_328767,RMVar_hsa_circ_333058,RMVar_hsa_circ_305585,RMVar_hsa_circ_255922,RMVar_hsa_circ_255923,RMVar_hsa_circ_255921,RMVar_hsa_circ_319550,RMVar_hsa_circ_282415,RMVar_hsa_circ_32033,RMVar_hsa_circ_311005,RMVar_hsa_circ_255924,RMVar_hsa_circ_7210,RMVar_hsa_circ_342562,RMVar_hsa_circ_352497,RMVar_hsa_circ_331894,RMVar_hsa_circ_255925,RMVar_hsa_circ_275458,RMVar_hsa_circ_355702,RMVar_hsa_circ_266838,RMVar_hsa_circ_49938,RMVar_hsa_circ_288144,RMVar_hsa_circ_362853,RMVar_hsa_circ_90936,RMVar_hsa_circ_255926 4816 RMVar_ID_4816 Human_SNP_ID_392694141 A-to-I Human chr9 - 19086404 19086404 19086404 GTTGGCCAGGCTGGTCTTGAACTCTTGAGCTCAGATGATCTGCATGCCTTGGCCTCCCAAAGTGC GTTGGCCAGGCTGGTCTTGAACTCTTGAGCTCCGATGATCTGCATGCCTTGGCCTCCCAAAGTGC T G HAUS6 Ensembl:ENSG00000147874 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1049672269 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16632412 RMVar_hsa_circ_255915,RMVar_hsa_circ_78693,RMVar_hsa_circ_45390,RMVar_hsa_circ_300056,RMVar_hsa_circ_13414,RMVar_hsa_circ_50374,RMVar_hsa_circ_23909,RMVar_hsa_circ_314919,RMVar_hsa_circ_286618,RMVar_hsa_circ_38223,RMVar_hsa_circ_255918,RMVar_hsa_circ_255920,RMVar_hsa_circ_112509,RMVar_hsa_circ_284016,RMVar_hsa_circ_328767,RMVar_hsa_circ_333058,RMVar_hsa_circ_305585,RMVar_hsa_circ_255922,RMVar_hsa_circ_255923,RMVar_hsa_circ_255921,RMVar_hsa_circ_319550,RMVar_hsa_circ_282415,RMVar_hsa_circ_32033,RMVar_hsa_circ_311005,RMVar_hsa_circ_255924,RMVar_hsa_circ_7210,RMVar_hsa_circ_342562,RMVar_hsa_circ_352497,RMVar_hsa_circ_331894,RMVar_hsa_circ_255925,RMVar_hsa_circ_275458,RMVar_hsa_circ_355702,RMVar_hsa_circ_266838,RMVar_hsa_circ_49938,RMVar_hsa_circ_288144,RMVar_hsa_circ_362853,RMVar_hsa_circ_90936,RMVar_hsa_circ_255926 4817 RMVar_ID_4817 Human_SNP_ID_392695550 A-to-I Human chr9 - 19090085 19090085 19090085 CCTGTAATCCCAGCACTCTGGGAGACTGAGACAGGAGGATCCCTTGAGTCCTGGAGTTCAAGACT CCTGTAATCCCAGCACTCTGGGAGACTGAGACGGGAGGATCCCTTGAGTCCTGGAGTTCAAGACT T C HAUS6 Ensembl:ENSG00000147874 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs905121770 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_300056,RMVar_hsa_circ_50374,RMVar_hsa_circ_314919,RMVar_hsa_circ_286618,RMVar_hsa_circ_255918,RMVar_hsa_circ_112509,RMVar_hsa_circ_284016,RMVar_hsa_circ_333058,RMVar_hsa_circ_255922,RMVar_hsa_circ_255923,RMVar_hsa_circ_282415,RMVar_hsa_circ_27289,RMVar_hsa_circ_255924,RMVar_hsa_circ_342562,RMVar_hsa_circ_331894,RMVar_hsa_circ_275458,RMVar_hsa_circ_355702,RMVar_hsa_circ_255929,RMVar_hsa_circ_288144,RMVar_hsa_circ_90936,RMVar_hsa_circ_336397,RMVar_hsa_circ_255926,RMVar_hsa_circ_273314 4818 RMVar_ID_4818 Human_SNP_ID_392695619 A-to-I Human chr9 - 19090336 19090336 19090336 AAAAGATTCTGTTTGGAAGCAAAGTAGCTCTTATTATAATTTGAGGTATCTATAAATAAATACAC AAAAGATTCTGTTTGGAAGCAAAGTAGCTCTTGTTATAATTTGAGGTATCTATAAATAAATACAC T C HAUS6 Ensembl:ENSG00000147874 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1054383426 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_300056,RMVar_hsa_circ_50374,RMVar_hsa_circ_314919,RMVar_hsa_circ_286618,RMVar_hsa_circ_255918,RMVar_hsa_circ_112509,RMVar_hsa_circ_284016,RMVar_hsa_circ_333058,RMVar_hsa_circ_255922,RMVar_hsa_circ_255923,RMVar_hsa_circ_282415,RMVar_hsa_circ_27289,RMVar_hsa_circ_255924,RMVar_hsa_circ_342562,RMVar_hsa_circ_331894,RMVar_hsa_circ_275458,RMVar_hsa_circ_355702,RMVar_hsa_circ_255929,RMVar_hsa_circ_288144,RMVar_hsa_circ_90936,RMVar_hsa_circ_336397,RMVar_hsa_circ_255926,RMVar_hsa_circ_273314 4819 RMVar_ID_4819 Human_SNP_ID_392695766 A-to-I Human chr9 - 19090638 19090638 19090638 GATTCTATGGCTGGGCGAGGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGTCAGGGCGGGC GATTCTATGGCTGGGCGAGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGTCAGGGCGGGC T C HAUS6 Ensembl:ENSG00000147874 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs571867655 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26215171 RMVar_hsa_circ_300056,RMVar_hsa_circ_50374,RMVar_hsa_circ_314919,RMVar_hsa_circ_286618,RMVar_hsa_circ_255918,RMVar_hsa_circ_112509,RMVar_hsa_circ_284016,RMVar_hsa_circ_333058,RMVar_hsa_circ_255922,RMVar_hsa_circ_255923,RMVar_hsa_circ_282415,RMVar_hsa_circ_27289,RMVar_hsa_circ_255924,RMVar_hsa_circ_342562,RMVar_hsa_circ_331894,RMVar_hsa_circ_275458,RMVar_hsa_circ_355702,RMVar_hsa_circ_255929,RMVar_hsa_circ_288144,RMVar_hsa_circ_90936,RMVar_hsa_circ_336397,RMVar_hsa_circ_255926,RMVar_hsa_circ_273314 4820 RMVar_ID_4820 Human_SNP_ID_392695945 A-to-I Human chr9 - 19091136 19091136 19091136 GCCACCATGCCTGCTAATTTTTTTGTATTTTTAGTATAGATGGGGTATCATTATGTTGGCCAGGC GCCACCATGCCTGCTAATTTTTTTGTATTTTTGGTATAGATGGGGTATCATTATGTTGGCCAGGC T C HAUS6 Ensembl:ENSG00000147874 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1390376057 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_300056,RMVar_hsa_circ_50374,RMVar_hsa_circ_314919,RMVar_hsa_circ_286618,RMVar_hsa_circ_255918,RMVar_hsa_circ_112509,RMVar_hsa_circ_284016,RMVar_hsa_circ_333058,RMVar_hsa_circ_255922,RMVar_hsa_circ_255923,RMVar_hsa_circ_282415,RMVar_hsa_circ_27289,RMVar_hsa_circ_255924,RMVar_hsa_circ_342562,RMVar_hsa_circ_331894,RMVar_hsa_circ_275458,RMVar_hsa_circ_355702,RMVar_hsa_circ_255929,RMVar_hsa_circ_288144,RMVar_hsa_circ_90936,RMVar_hsa_circ_336397,RMVar_hsa_circ_255926,RMVar_hsa_circ_273314 4821 RMVar_ID_4821 Human_SNP_ID_392695971 A-to-I Human chr9 - 19091217 19091217 19091217 CGGCTTACTGCAACATCCACTTCCCGGGTTCAAGCGATTCTACTGCTTCAGCCTTCCGAGTAGCT CGGCTTACTGCAACATCCACTTCCCGGGTTCAGGCGATTCTACTGCTTCAGCCTTCCGAGTAGCT T C HAUS6 Ensembl:ENSG00000147874 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1053600565 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18907046 RMVar_hsa_circ_300056,RMVar_hsa_circ_50374,RMVar_hsa_circ_314919,RMVar_hsa_circ_286618,RMVar_hsa_circ_255918,RMVar_hsa_circ_112509,RMVar_hsa_circ_284016,RMVar_hsa_circ_333058,RMVar_hsa_circ_255922,RMVar_hsa_circ_255923,RMVar_hsa_circ_282415,RMVar_hsa_circ_27289,RMVar_hsa_circ_255924,RMVar_hsa_circ_342562,RMVar_hsa_circ_331894,RMVar_hsa_circ_275458,RMVar_hsa_circ_355702,RMVar_hsa_circ_255929,RMVar_hsa_circ_288144,RMVar_hsa_circ_90936,RMVar_hsa_circ_336397,RMVar_hsa_circ_255926,RMVar_hsa_circ_273314 4822 RMVar_ID_4822 Human_SNP_ID_392695982 A-to-I Human chr9 - 19091237 19091237 19091237 GGAGTGCGGTGGCGCGATCTCGGCTTACTGCAACATCCACTTCCCGGGTTCAAGCGATTCTACTG GGAGTGCGGTGGCGCGATCTCGGCTTACTGCAGCATCCACTTCCCGGGTTCAAGCGATTCTACTG T C HAUS6 Ensembl:ENSG00000147874 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1248368634 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_300056,RMVar_hsa_circ_50374,RMVar_hsa_circ_314919,RMVar_hsa_circ_286618,RMVar_hsa_circ_255918,RMVar_hsa_circ_112509,RMVar_hsa_circ_284016,RMVar_hsa_circ_333058,RMVar_hsa_circ_255922,RMVar_hsa_circ_255923,RMVar_hsa_circ_282415,RMVar_hsa_circ_27289,RMVar_hsa_circ_255924,RMVar_hsa_circ_342562,RMVar_hsa_circ_331894,RMVar_hsa_circ_275458,RMVar_hsa_circ_355702,RMVar_hsa_circ_255929,RMVar_hsa_circ_288144,RMVar_hsa_circ_90936,RMVar_hsa_circ_336397,RMVar_hsa_circ_255926,RMVar_hsa_circ_273314 4823 RMVar_ID_4823 Human_SNP_ID_392696344 A-to-I Human chr9 - 19092272 19092264 19092273 GTTTTTTTTTTTTAATACCAGGGTTACACCATATTTCCCAGGCTGGTCTTGAACCCCTGTGCTCA GTTTTTTTTTTTTAATACCAGGGTTACACCA_________GGCTGGTCTTGAACCCCTGTGCTCA CTGGGAAATA C HAUS6 Ensembl:ENSG00000147874 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1362812812 Functional Loss DEL dbSNP153 32..40 33 - - - Human_RBP_ID_17579628,Human_RBP_ID_23201051 RMVar_hsa_circ_300056,RMVar_hsa_circ_50374,RMVar_hsa_circ_314919,RMVar_hsa_circ_286618,RMVar_hsa_circ_255918,RMVar_hsa_circ_112509,RMVar_hsa_circ_284016,RMVar_hsa_circ_333058,RMVar_hsa_circ_255922,RMVar_hsa_circ_255923,RMVar_hsa_circ_282415,RMVar_hsa_circ_27289,RMVar_hsa_circ_255924,RMVar_hsa_circ_342562,RMVar_hsa_circ_331894,RMVar_hsa_circ_275458,RMVar_hsa_circ_355702,RMVar_hsa_circ_255929,RMVar_hsa_circ_288144,RMVar_hsa_circ_90936,RMVar_hsa_circ_336397,RMVar_hsa_circ_255926,RMVar_hsa_circ_273314 4824 RMVar_ID_4824 Human_SNP_ID_392696346 A-to-I Human chr9 - 19092272 19092272 19092272 GTTTTTTTTTTTTAATACCAGGGTTACACCATATTTCCCAGGCTGGTCTTGAACCCCTGTGCTCA GTTTTTTTTTTTTAATACCAGGGTTACACCATGTTTCCCAGGCTGGTCTTGAACCCCTGTGCTCA T C HAUS6 Ensembl:ENSG00000147874 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs111909375 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17579628,Human_RBP_ID_23201051 RMVar_hsa_circ_300056,RMVar_hsa_circ_50374,RMVar_hsa_circ_314919,RMVar_hsa_circ_286618,RMVar_hsa_circ_255918,RMVar_hsa_circ_112509,RMVar_hsa_circ_284016,RMVar_hsa_circ_333058,RMVar_hsa_circ_255922,RMVar_hsa_circ_255923,RMVar_hsa_circ_282415,RMVar_hsa_circ_27289,RMVar_hsa_circ_255924,RMVar_hsa_circ_342562,RMVar_hsa_circ_331894,RMVar_hsa_circ_275458,RMVar_hsa_circ_355702,RMVar_hsa_circ_255929,RMVar_hsa_circ_288144,RMVar_hsa_circ_90936,RMVar_hsa_circ_336397,RMVar_hsa_circ_255926,RMVar_hsa_circ_273314 4825 RMVar_ID_4825 Human_SNP_ID_392699038 A-to-I Human chr9 - 19099447 19099447 19099447 AAAAACAAAAAAGAGGCCGGGTGCGGTGGCTCACGCCTGTAATTCCAGCACTTTGGGAGGCCGAG AAAAACAAAAAAGAGGCCGGGTGCGGTGGCTCGCGCCTGTAATTCCAGCACTTTGGGAGGCCGAG T C HAUS6 Ensembl:ENSG00000147874 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1420258785 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90936,RMVar_hsa_circ_255926 4826 RMVar_ID_4826 Human_SNP_ID_392699135 A-to-I Human chr9 - 19099720 19099720 19099720 ATTGCTCGATGCATTTGTAAATCCAGCTACTCAGAAGGCTGAGGTGGGAGATTGCTTGAGGCCAG ATTGCTCGATGCATTTGTAAATCCAGCTACTCGGAAGGCTGAGGTGGGAGATTGCTTGAGGCCAG T C HAUS6 Ensembl:ENSG00000147874 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1433173847 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16632783,Human_RBP_ID_17579441 RMVar_hsa_circ_90936,RMVar_hsa_circ_255926 4827 RMVar_ID_4827 Human_SNP_ID_392699268 A-to-I Human chr9 - 19100107 19100107 19100107 TCACTGCAACCCCCGCCTCCCTGGTTCAAGCAATTCTCTGCCTCAGCCTCCTGAGTAGCTGGGAA TCACTGCAACCCCCGCCTCCCTGGTTCAAGCAGTTCTCTGCCTCAGCCTCCTGAGTAGCTGGGAA T C HAUS6 Ensembl:ENSG00000147874 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs556988156 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90936,RMVar_hsa_circ_255926 4828 RMVar_ID_4828 Human_SNP_ID_392699270 A-to-I Human chr9 - 19100111 19100111 19100111 GGACTCACTGCAACCCCCGCCTCCCTGGTTCAAGCAATTCTCTGCCTCAGCCTCCTGAGTAGCTG GGACTCACTGCAACCCCCGCCTCCCTGGTTCAGGCAATTCTCTGCCTCAGCCTCCTGAGTAGCTG T C HAUS6 Ensembl:ENSG00000147874 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1231648346 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90936,RMVar_hsa_circ_255926 4829 RMVar_ID_4829 Human_SNP_ID_392699338 A-to-I Human chr9 - 19100304 19100304 19100304 TGGAGTGCAGTGGCCTGAATGTGGCTCACTGCAGCCTCCATCTCCTGGGCTCAAGCGATCCTTCC TGGAGTGCAGTGGCCTGAATGTGGCTCACTGCGGCCTCCATCTCCTGGGCTCAAGCGATCCTTCC T C HAUS6 Ensembl:ENSG00000147874 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1021847453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16632794 RMVar_hsa_circ_90936,RMVar_hsa_circ_255926 4830 RMVar_ID_4830 Human_SNP_ID_392699339 A-to-I Human chr9 - 19100304 19100304 19100304 TGGAGTGCAGTGGCCTGAATGTGGCTCACTGCAGCCTCCATCTCCTGGGCTCAAGCGATCCTTCC TGGAGTGCAGTGGCCTGAATGTGGCTCACTGCCGCCTCCATCTCCTGGGCTCAAGCGATCCTTCC T G HAUS6 Ensembl:ENSG00000147874 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1021847453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16632794 RMVar_hsa_circ_90936,RMVar_hsa_circ_255926 4831 RMVar_ID_4831 Human_SNP_ID_392703327 A-to-I Human chr9 - 19112506 19112500 19112506 TGGGGTTTCACCATGTTGCCCAGGCTGGTCTCAAACTCCTGAGCTCAAGTGATCCACTCACCTCG TGGGGTTTCACCATGTTGCCCAGGCTGGTCTC______CTGAGCTCAAGTGATCCACTCACCTCG GGAGTTT G PLIN2 Ensembl:ENSG00000147872 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1426395975 Functional Loss DEL dbSNP153 33..38 33 - - - 4832 RMVar_ID_4832 Human_SNP_ID_392703994 A-to-I Human chr9 - 19114683 19114683 19114683 ACTTGTGAAATAGGCCAGGCGCTGTGGCTCATACCTGTAATCCCAGCACTTTGGGAGGCCGAGGC ACTTGTGAAATAGGCCAGGCGCTGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGC T C PLIN2 Ensembl:ENSG00000147872 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1041384095 Functional Loss SNV dbSNP153 33..33 33 - - - 4833 RMVar_ID_4833 Human_SNP_ID_392707214 A-to-I Human chr9 - 19125559 19125559 19125559 CCCAGAGGATGGGCACGGTGGCCTGCACCTGTAATCCTAGCACTTTGGGAGGTCTAGATGGGAGG CCCAGAGGATGGGCACGGTGGCCTGCACCTGTTATCCTAGCACTTTGGGAGGTCTAGATGGGAGG T A PLIN2 Ensembl:ENSG00000147872 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs573598660 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17579231 RMVar_hsa_circ_83176,RMVar_hsa_circ_255934,RMVar_hsa_circ_267093 4834 RMVar_ID_4834 Human_SNP_ID_392741071 A-to-I Human chr9 - 19227495 19227494 19227495 AAATTAGCCAGATATGGTGGTGGGTGCCTGTAATCTCAGCTACTAGGGAGGCTGAGACAGGAGAA AAATTAGCCAGATATGGTGGTGGGTGCCTGTA_TCTCAGCTACTAGGGAGGCTGAGACAGGAGAA AT A RF00017-4620,RF00017-4565 RNACentral:URS000092122F,RNACentral:URS000096E4F6 SRP RNA,SRP RNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1397794412 Functional Loss DEL dbSNP153 33..33 33 - - - 4835 RMVar_ID_4835 Human_SNP_ID_392769972 A-to-I Human chr9 + 19314997 19314997 19314997 CAGCCTGGACAACATGATGAAACCCTGTCTCTACTAAAATAAAAAATTAGCTGGGCGTGATGGCG CAGCCTGGACAACATGATGAAACCCTGTCTCTTCTAAAATAAAAAATTAGCTGGGCGTGATGGCG A T DENND4C Ensembl:ENSG00000137145 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs540173026 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8709,RMVar_hsa_circ_31874,RMVar_hsa_circ_48603,RMVar_hsa_circ_324926,RMVar_hsa_circ_331686,RMVar_hsa_circ_308433,RMVar_hsa_circ_255944,RMVar_hsa_circ_255945,RMVar_hsa_circ_292985,RMVar_hsa_circ_336113,RMVar_hsa_circ_360363,RMVar_hsa_circ_319117,RMVar_hsa_circ_255948,RMVar_hsa_circ_13038,RMVar_hsa_circ_255946,RMVar_hsa_circ_255947,RMVar_hsa_circ_337631,RMVar_hsa_circ_296477,RMVar_hsa_circ_288356,RMVar_hsa_circ_45406,RMVar_hsa_circ_255960,RMVar_hsa_circ_294471,RMVar_hsa_circ_255956,RMVar_hsa_circ_255957,RMVar_hsa_circ_255958,RMVar_hsa_circ_255955,RMVar_hsa_circ_300200,RMVar_hsa_circ_312350,RMVar_hsa_circ_318481,RMVar_hsa_circ_297646,RMVar_hsa_circ_10846,RMVar_hsa_circ_273776,RMVar_hsa_circ_35560,RMVar_hsa_circ_255962,RMVar_hsa_circ_255961,RMVar_hsa_circ_269546,RMVar_hsa_circ_367092,RMVar_hsa_circ_255959,RMVar_hsa_circ_335513,RMVar_hsa_circ_64246,RMVar_hsa_circ_266346,RMVar_hsa_circ_99130,RMVar_hsa_circ_255967,RMVar_hsa_circ_316264,RMVar_hsa_circ_321445,RMVar_hsa_circ_60150,RMVar_hsa_circ_76980,RMVar_hsa_circ_22364,RMVar_hsa_circ_255969,RMVar_hsa_circ_255971,RMVar_hsa_circ_255970,RMVar_hsa_circ_255968,RMVar_hsa_circ_255975,RMVar_hsa_circ_299938,RMVar_hsa_circ_359177,RMVar_hsa_circ_301617,RMVar_hsa_circ_255976 4836 RMVar_ID_4836 Human_SNP_ID_392771929 A-to-I Human chr9 + 19320364 19320364 19320364 GGGATTACAGGCGCGCACCACCATGCCTGGCTAATTTTTGTATTTTAAGTGGAGATGAGGTTTAG GGGATTACAGGCGCGCACCACCATGCCTGGCTGATTTTTGTATTTTAAGTGGAGATGAGGTTTAG A G DENND4C Ensembl:ENSG00000137145 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1197940588 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8709,RMVar_hsa_circ_31874,RMVar_hsa_circ_48603,RMVar_hsa_circ_331686,RMVar_hsa_circ_308433,RMVar_hsa_circ_255945,RMVar_hsa_circ_336113,RMVar_hsa_circ_360363,RMVar_hsa_circ_319117,RMVar_hsa_circ_13038,RMVar_hsa_circ_255946,RMVar_hsa_circ_255947,RMVar_hsa_circ_337631,RMVar_hsa_circ_288356,RMVar_hsa_circ_45406,RMVar_hsa_circ_255960,RMVar_hsa_circ_255956,RMVar_hsa_circ_255957,RMVar_hsa_circ_255958,RMVar_hsa_circ_300200,RMVar_hsa_circ_312350,RMVar_hsa_circ_318481,RMVar_hsa_circ_297646,RMVar_hsa_circ_10846,RMVar_hsa_circ_273776,RMVar_hsa_circ_35560,RMVar_hsa_circ_255961,RMVar_hsa_circ_269546,RMVar_hsa_circ_255959,RMVar_hsa_circ_335513,RMVar_hsa_circ_64246,RMVar_hsa_circ_266346,RMVar_hsa_circ_99130,RMVar_hsa_circ_255967,RMVar_hsa_circ_321445,RMVar_hsa_circ_60150,RMVar_hsa_circ_76980,RMVar_hsa_circ_22364,RMVar_hsa_circ_22011,RMVar_hsa_circ_255969,RMVar_hsa_circ_255970,RMVar_hsa_circ_255968,RMVar_hsa_circ_359177,RMVar_hsa_circ_301617,RMVar_hsa_circ_255976,RMVar_hsa_circ_45483,RMVar_hsa_circ_329659,RMVar_hsa_circ_361314,RMVar_hsa_circ_322204,RMVar_hsa_circ_54219,RMVar_hsa_circ_29105,RMVar_hsa_circ_255978,RMVar_hsa_circ_13148,RMVar_hsa_circ_255979 4837 RMVar_ID_4837 Human_SNP_ID_392774376 A-to-I Human chr9 + 19328502 19328502 19328502 GGGCGTGGTGTCAGGCGCCTGTGATCCCAGCTACTCGGGAGGCTAAGGCAGGAGAATCGCTTGAA GGGCGTGGTGTCAGGCGCCTGTGATCCCAGCTCCTCGGGAGGCTAAGGCAGGAGAATCGCTTGAA A C DENND4C Ensembl:ENSG00000137145 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1203700309 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8709,RMVar_hsa_circ_31874,RMVar_hsa_circ_48603,RMVar_hsa_circ_331686,RMVar_hsa_circ_255945,RMVar_hsa_circ_360363,RMVar_hsa_circ_13038,RMVar_hsa_circ_255946,RMVar_hsa_circ_337631,RMVar_hsa_circ_45406,RMVar_hsa_circ_255957,RMVar_hsa_circ_255958,RMVar_hsa_circ_312350,RMVar_hsa_circ_297646,RMVar_hsa_circ_10846,RMVar_hsa_circ_273776,RMVar_hsa_circ_35560,RMVar_hsa_circ_255959,RMVar_hsa_circ_335513,RMVar_hsa_circ_266346,RMVar_hsa_circ_255967,RMVar_hsa_circ_60150,RMVar_hsa_circ_76980,RMVar_hsa_circ_22364,RMVar_hsa_circ_22011,RMVar_hsa_circ_255968,RMVar_hsa_circ_359177,RMVar_hsa_circ_45483,RMVar_hsa_circ_329659,RMVar_hsa_circ_31116,RMVar_hsa_circ_13148,RMVar_hsa_circ_255979,RMVar_hsa_circ_364369,RMVar_hsa_circ_114201,RMVar_hsa_circ_255981,RMVar_hsa_circ_322961,RMVar_hsa_circ_332994,RMVar_hsa_circ_344133,RMVar_hsa_circ_58244,RMVar_hsa_circ_255982,RMVar_hsa_circ_255983 4838 RMVar_ID_4838 Human_SNP_ID_392787718 A-to-I Human chr9 + 19373161 19373161 19373161 ATTAATTGTAGTTTTTGCCACTATTAATGGCAAAAACCGCAATTATTTTTGTACCAACATAATAC ATTAATTGTAGTTTTTGCCACTATTAATGGCAGAAACCGCAATTATTTTTGTACCAACATAATAC A G DENND4C Ensembl:ENSG00000137145 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs554258280 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_187643 4839 RMVar_ID_4839 Human_SNP_ID_392787766 A-to-I Human chr9 - 19373281 19373281 19373281 ATGATTGATTCATTTGTTCCCATTTTAAAACTATTGCAAATTAACATTGGGAAGAGGATGGAAGT ATGATTGATTCATTTGTTCCCATTTTAAAACTGTTGCAAATTAACATTGGGAAGAGGATGGAAGT T C RF00017-4565 RNACentral:URS000096E4F6 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1311440488 Functional Loss SNV dbSNP153 33..33 33 - - - 4840 RMVar_ID_4840 Human_SNP_ID_392787767 A-to-I Human chr9 - 19373281 19373281 19373281 ATGATTGATTCATTTGTTCCCATTTTAAAACTATTGCAAATTAACATTGGGAAGAGGATGGAAGT ATGATTGATTCATTTGTTCCCATTTTAAAACTCTTGCAAATTAACATTGGGAAGAGGATGGAAGT T G RF00017-4565 RNACentral:URS000096E4F6 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1311440488 Functional Loss SNV dbSNP153 33..33 33 - - - 4841 RMVar_ID_4841 Human_SNP_ID_392788560 A-to-I Human chr9 - 19375207 19375207 19375207 CAACATGGTGAAACCCCGTTCCTACTAAAAATACGAAAATTAGCGCATGCCTGTAGTCCCAGCTA CAACATGGTGAAACCCCGTTCCTACTAAAAATGCGAAAATTAGCGCATGCCTGTAGTCCCAGCTA T C RF00017-4565 RNACentral:URS000096E4F6 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1324931937 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3198775,Human_RBP_ID_16634252 4842 RMVar_ID_4842 Human_SNP_ID_392788627 A-to-I Human chr9 - 19375349 19375349 19375349 GTTAAAAAGCTACATAACATGAAAAGAATCTTAGTTGGCAATCAATAATAATATGCAGAACTTAA GTTAAAAAGCTACATAACATGAAAAGAATCTTGGTTGGCAATCAATAATAATATGCAGAACTTAA T C RF00017-4565 RNACentral:URS000096E4F6 SRP RNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1463861127 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16634259,Human_RBP_ID_17436039,Human_RBP_ID_17716383,Human_RBP_ID_18133592,Human_RBP_ID_18397574,Human_RBP_ID_27545170,Human_RBP_ID_27784634 4843 RMVar_ID_4843 Human_SNP_ID_392812521 A-to-I Human chr9 + 19448120 19448120 19448120 TCTCTGCCTCCCGGACTGAAAGTGATTCTCCCACCTCACCCCCTGCAGGGAGCTGGGACTACAGG TCTCTGCCTCCCGGACTGAAAGTGATTCTCCCTCCTCACCCCCTGCAGGGAGCTGGGACTACAGG A T ACER2 Ensembl:ENSG00000177076 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909776289 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89379,RMVar_hsa_circ_256014 4844 RMVar_ID_4844 Human_SNP_ID_392882564 A-to-I Human chr9 - 19666330 19666330 19666330 GCAATCACAACTCACTGCAGCCTCAACCTCCCAGGCTCAGGTGATCCTTCCACCTCAGCCTCTTG GCAATCACAACTCACTGCAGCCTCAACCTCCCGGGCTCAGGTGATCCTTCCACCTCAGCCTCTTG T C SLC24A2 Ensembl:ENSG00000155886 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1329967156 Functional Loss SNV dbSNP153 33..33 33 - - - 4845 RMVar_ID_4845 Human_SNP_ID_393091178 A-to-I Human chr9 - 20345906 20345906 20345906 TGCCATCCCAAGCCCAGTGACCTTACTCGTATACCGTGCCACTTTCCACCAACTTTTTCCAAGTC TGCCATCCCAAGCCCAGTGACCTTACTCGTATGCCGTGCCACTTTCCACCAACTTTTTCCAAGTC T C MLLT3 Ensembl:ENSG00000171843 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs989984298 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17201915,Human_RBP_ID_21659279 Human_miRNA_ID_1687895 RMVar_hsa_circ_256022 4846 RMVar_ID_4846 Human_SNP_ID_393139719 A-to-I Human chr9 - 20525444 20525444 20525444 TTGCCCAGGCTGGAGTGCAGTGGCAGGATCTCAGCACACTGTAACCTCCGCCTTCCGGGTTCAAG TTGCCCAGGCTGGAGTGCAGTGGCAGGATCTCGGCACACTGTAACCTCCGCCTTCCGGGTTCAAG T C MLLT3 Ensembl:ENSG00000171843 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1029664625 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16637192,Human_RBP_ID_26216129 RMVar_hsa_circ_55174 4847 RMVar_ID_4847 Human_SNP_ID_393148512 A-to-I Human chr9 - 20556620 20556620 20556620 GGAGTGCAGTGGTGCGATCTCGGATCACTGCAACCTCCTACTCTTGGGTTCAAGGGATTTTTCTG GGAGTGCAGTGGTGCGATCTCGGATCACTGCAGCCTCCTACTCTTGGGTTCAAGGGATTTTTCTG T C MLLT3 Ensembl:ENSG00000171843 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs542361865 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7914799,Human_RBP_ID_16637897 RMVar_hsa_circ_55174 4848 RMVar_ID_4848 Human_SNP_ID_393153327 A-to-I Human chr9 - 20573373 20573373 20573373 GAGTTCGAGACTAGTCTGGGCAACATGGTGAAACCCATCTTTATGAAAAATACAGAAAATTAGCC GAGTTCGAGACTAGTCTGGGCAACATGGTGAATCCCATCTTTATGAAAAATACAGAAAATTAGCC T A MLLT3 Ensembl:ENSG00000171843 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1369579607 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17579235 RMVar_hsa_circ_55174 4849 RMVar_ID_4849 Human_SNP_ID_393153863 A-to-I Human chr9 - 20575406 20575406 20575406 TTTAATTTTAAAAATGCTTTATTGCTAAAAAAATTGCTAATGATCATCTGGGTCTTCTGCGAGTT TTTAATTTTAAAAATGCTTTATTGCTAAAAAATTTGCTAATGATCATCTGGGTCTTCTGCGAGTT T A MLLT3 Ensembl:ENSG00000171843 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1177795800 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3897449,Human_RBP_ID_8701774 RMVar_hsa_circ_55174 4850 RMVar_ID_4850 Human_SNP_ID_393153864 A-to-I Human chr9 - 20575412 20575412 20575412 AAAAAATTTAATTTTAAAAATGCTTTATTGCTAAAAAAATTGCTAATGATCATCTGGGTCTTCTG AAAAAATTTAATTTTAAAAATGCTTTATTGCTTAAAAAATTGCTAATGATCATCTGGGTCTTCTG T A MLLT3 Ensembl:ENSG00000171843 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1008383063 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3897449,Human_RBP_ID_8701774,Human_RBP_ID_16638382 RMVar_hsa_circ_55174 4851 RMVar_ID_4851 Human_SNP_ID_393184893 A-to-I Human chr9 + 20681370 20681370 20681370 CCTCCCACTTGGCCTCCCAAAGTGCTGGGATTATAGGTGTGAGCCATCATGCCCGGCCTGAGAGG CCTCCCACTTGGCCTCCCAAAGTGCTGGGATTTTAGGTGTGAGCCATCATGCCCGGCCTGAGAGG A T FOCAD Ensembl:ENSG00000188352 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1298850046 Functional Loss SNV dbSNP153 33..33 33 - - - 4852 RMVar_ID_4852 Human_SNP_ID_393189728 A-to-I Human chr9 + 20698648 20698648 20698648 ACTTGAAATCAGCCTCCCAAAGTGTTGGGATTACAGGTGTGAGCCACTGCGCCCGGCTTATGTTT ACTTGAAATCAGCCTCCCAAAGTGTTGGGATTGCAGGTGTGAGCCACTGCGCCCGGCTTATGTTT A G FOCAD Ensembl:ENSG00000188352 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1317336055 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23325,RMVar_hsa_circ_273604,RMVar_hsa_circ_354095,RMVar_hsa_circ_373736,RMVar_hsa_circ_355897,RMVar_hsa_circ_324080,RMVar_hsa_circ_71117,RMVar_hsa_circ_110637,RMVar_hsa_circ_49376,RMVar_hsa_circ_256047,RMVar_hsa_circ_256048,RMVar_hsa_circ_256049 4853 RMVar_ID_4853 Human_SNP_ID_393199869 A-to-I Human chr9 + 20733878 20733878 20733878 AAAAAATTAGCCAGGTATGGTGATGCACACCTATAGCTCCAGATACTTGGGAGGCTTAGGTTCGA AAAAAATTAGCCAGGTATGGTGATGCACACCTGTAGCTCCAGATACTTGGGAGGCTTAGGTTCGA A G FOCAD Ensembl:ENSG00000188352 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs758351843 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23325,RMVar_hsa_circ_273604,RMVar_hsa_circ_354095,RMVar_hsa_circ_373736,RMVar_hsa_circ_355897,RMVar_hsa_circ_71117,RMVar_hsa_circ_110637,RMVar_hsa_circ_49376,RMVar_hsa_circ_9436,RMVar_hsa_circ_109343,RMVar_hsa_circ_16288,RMVar_hsa_circ_282554,RMVar_hsa_circ_289053,RMVar_hsa_circ_301642,RMVar_hsa_circ_256048,RMVar_hsa_circ_256049,RMVar_hsa_circ_323802,RMVar_hsa_circ_363847,RMVar_hsa_circ_319539,RMVar_hsa_circ_293575,RMVar_hsa_circ_290049,RMVar_hsa_circ_287425,RMVar_hsa_circ_288553,RMVar_hsa_circ_284948,RMVar_hsa_circ_88923,RMVar_hsa_circ_275433,RMVar_hsa_circ_275832,RMVar_hsa_circ_97768,RMVar_hsa_circ_49116,RMVar_hsa_circ_72042,RMVar_hsa_circ_18597,RMVar_hsa_circ_256053,RMVar_hsa_circ_256057,RMVar_hsa_circ_256059,RMVar_hsa_circ_256060,RMVar_hsa_circ_256058,RMVar_hsa_circ_256055,RMVar_hsa_circ_256056,RMVar_hsa_circ_256054,RMVar_hsa_circ_346443,RMVar_hsa_circ_256051,RMVar_hsa_circ_256052,RMVar_hsa_circ_359621,RMVar_hsa_circ_256050,RMVar_hsa_circ_354190,RMVar_hsa_circ_337218,RMVar_hsa_circ_343113,RMVar_hsa_circ_308176,RMVar_hsa_circ_31425,RMVar_hsa_circ_88513,RMVar_hsa_circ_91452,RMVar_hsa_circ_62568,RMVar_hsa_circ_66508,RMVar_hsa_circ_99396,RMVar_hsa_circ_256063,RMVar_hsa_circ_256064,RMVar_hsa_circ_256062,RMVar_hsa_circ_75789,RMVar_hsa_circ_17197,RMVar_hsa_circ_256065,RMVar_hsa_circ_256066 4854 RMVar_ID_4854 Human_SNP_ID_393273482 A-to-I Human chr9 + 20983418 20983418 20983418 ACATGGTGAAACCCCGTCTCTACTAAAGGTACAAAAATTAGCTGGGCGTAGTGGCACACACCTGT ACATGGTGAAACCCCGTCTCTACTAAAGGTACGAAAATTAGCTGGGCGTAGTGGCACACACCTGT A G FOCAD Ensembl:ENSG00000188352 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs563855517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_183802 RMVar_hsa_circ_123825,RMVar_hsa_circ_256074,RMVar_hsa_circ_81004,RMVar_hsa_circ_256098,RMVar_hsa_circ_82134,RMVar_hsa_circ_256100,RMVar_hsa_circ_24677,RMVar_hsa_circ_101740,RMVar_hsa_circ_111191,RMVar_hsa_circ_105563,RMVar_hsa_circ_256125,RMVar_hsa_circ_256123,RMVar_hsa_circ_256124,RMVar_hsa_circ_54347,RMVar_hsa_circ_104115,RMVar_hsa_circ_85807,RMVar_hsa_circ_256143,RMVar_hsa_circ_338510,RMVar_hsa_circ_256154,RMVar_hsa_circ_256153,RMVar_hsa_circ_87893,RMVar_hsa_circ_370755,RMVar_hsa_circ_256164,RMVar_hsa_circ_256165,RMVar_hsa_circ_256166,RMVar_hsa_circ_33192,RMVar_hsa_circ_372123 4855 RMVar_ID_4855 Human_SNP_ID_393525139 A-to-I Human chr9 + 21808925 21808925 21808925 CATGTGAAGACACATGGAGAACGCTGCCATCTACAAGCCAAGGAGACTGACCTTAGAAGAAATCA CATGTGAAGACACATGGAGAACGCTGCCATCTGCAAGCCAAGGAGACTGACCTTAGAAGAAATCA A G AL359922.1,MTAP Ensembl:ENSG00000264545,Ensembl:ENSG00000099810 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs746912720 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1035519 RMVar_hsa_circ_256177,RMVar_hsa_circ_127908 4856 RMVar_ID_4856 Human_SNP_ID_393525504 A-to-I Human chr9 + 21810213 21810213 21810213 AGGTGAGATCAAGGTGGATTTCTTGTAAGGTCAGTCTGCTTGGCTTGTACATGGCAATGTTCTCC AGGTGAGATCAAGGTGGATTTCTTGTAAGGTCTGTCTGCTTGGCTTGTACATGGCAATGTTCTCC A T AL359922.1,MTAP Ensembl:ENSG00000264545,Ensembl:ENSG00000099810 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1417306932 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_256177,RMVar_hsa_circ_127908 4857 RMVar_ID_4857 Human_SNP_ID_393541608 A-to-I Human chr9 + 21865373 21865373 21865373 CTTCCCAGCTATGTGGAACTGTGAGTTAATTAAACCTCTTTCCTTTATAAATTACCCAGTCATGG CTTCCCAGCTATGTGGAACTGTGAGTTAATTACACCTCTTTCCTTTATAAATTACCCAGTCATGG A C AL359922.1,MTAP Ensembl:ENSG00000264545,Ensembl:ENSG00000099810 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs945811769 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3202596,Human_RBP_ID_21659435 Human_miRNA_ID_1754948,Human_miRNA_ID_2448489 RMVar_hsa_circ_256177,RMVar_hsa_circ_127908,RMVar_hsa_circ_107351,RMVar_hsa_circ_256180,RMVar_hsa_circ_256179 4858 RMVar_ID_4858 Human_SNP_ID_393541751 A-to-I Human chr9 + 21865870 21865870 21865870 GTGCCTTTTTTATTGCCTAGTAGTATTCTGTCATATGCCTATCTTACAATTTGATTATCTATTCA GTGCCTTTTTTATTGCCTAGTAGTATTCTGTCGTATGCCTATCTTACAATTTGATTATCTATTCA A G AL359922.1,MTAP Ensembl:ENSG00000264545,Ensembl:ENSG00000099810 Protein coding,Protein coding intron,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs534675057 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1704386,Human_RBP_ID_2063338,Human_RBP_ID_3202603,Human_RBP_ID_3897915,Human_RBP_ID_7916369,Human_RBP_ID_8702145,Human_RBP_ID_16642910,Human_RBP_ID_27784818 Human_miRNA_ID_1248249 RMVar_hsa_circ_256177,RMVar_hsa_circ_127908,RMVar_hsa_circ_107351,RMVar_hsa_circ_256180,RMVar_hsa_circ_256179 4859 RMVar_ID_4859 Human_SNP_ID_393561344 A-to-I Human chr9 + 21937119 21937119 21937119 TCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGCAGATCATGAGGTCAAGAGATCAAG TCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCAGATCATGAGGTCAAGAGATCAAG A G AL359922.1,MTAP Ensembl:ENSG00000264545,Ensembl:ENSG00000099810 Protein coding,Protein coding intron,3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs951394577 Functional Loss SNV dbSNP153 33..33 33 - - - 4860 RMVar_ID_4860 Human_SNP_ID_393588327 A-to-I Human chr9 + 22032763 22032763 22032763 ATTTTTCCTGCAGGGATTCCCTCTACAAAATTAAAAACACTGGGCATGTGGAAATAATATTCATG ATTTTTCCTGCAGGGATTCCCTCTACAAAATTGAAAACACTGGGCATGTGGAAATAATATTCATG A G CDKN2B-AS1 Ensembl:ENSG00000240498 lincRNA exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1157385175 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3203545,Human_RBP_ID_10427246 Human_Splice_Rec_1035606,Human_Splice_Rec_1035614,Human_Splice_Rec_1035618,Human_Splice_Rec_1035704 RMVar_hsa_circ_35900,RMVar_hsa_circ_256182,RMVar_hsa_circ_111947,RMVar_hsa_circ_338946,RMVar_hsa_circ_359038,RMVar_hsa_circ_302525,RMVar_hsa_circ_20555,RMVar_hsa_circ_31549,RMVar_hsa_circ_357564 4861 RMVar_ID_4861 Human_SNP_ID_393588328 A-to-I Human chr9 + 22032764 22032764 22032764 TTTTTCCTGCAGGGATTCCCTCTACAAAATTAAAAACACTGGGCATGTGGAAATAATATTCATGC TTTTTCCTGCAGGGATTCCCTCTACAAAATTAGAAACACTGGGCATGTGGAAATAATATTCATGC A G CDKN2B-AS1 Ensembl:ENSG00000240498 lincRNA exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1007631245 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3203545,Human_RBP_ID_10427246 Human_Splice_Rec_1035606,Human_Splice_Rec_1035614,Human_Splice_Rec_1035618,Human_Splice_Rec_1035704 RMVar_hsa_circ_35900,RMVar_hsa_circ_256182,RMVar_hsa_circ_111947,RMVar_hsa_circ_338946,RMVar_hsa_circ_359038,RMVar_hsa_circ_302525,RMVar_hsa_circ_20555,RMVar_hsa_circ_31549,RMVar_hsa_circ_357564 4862 RMVar_ID_4862 Human_SNP_ID_393588355 A-to-I Human chr9 + 22032900 22032900 22032900 AGTGAATAGAAAAGACAATTTAAAGCGTGAATATTATTTCCTCATGCCCAGTGTTTTTAATTTTG AGTGAATAGAAAAGACAATTTAAAGCGTGAATTTTATTTCCTCATGCCCAGTGTTTTTAATTTTG A T CDKN2B-AS1 Ensembl:ENSG00000240498 lincRNA exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1207758682 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5251848 Human_Splice_Rec_1035619,Human_Splice_Rec_1035705 RMVar_hsa_circ_35900,RMVar_hsa_circ_256182,RMVar_hsa_circ_111947,RMVar_hsa_circ_338946,RMVar_hsa_circ_359038,RMVar_hsa_circ_302525,RMVar_hsa_circ_20555,RMVar_hsa_circ_31549,RMVar_hsa_circ_357564 4863 RMVar_ID_4863 Human_SNP_ID_393597064 A-to-I Human chr9 + 22066718 22066717 22066719 TAAAAAGAACATTCGTATTTTAATTTTAGCATAGAGTTACCATCGGGTCTTAGAAATTCTCAGAA TAAAAAGAACATTCGTATTTTAATTTTAGCAT__AGTTACCATCGGGTCTTAGAAATTCTCAGAA TAG T CDKN2B-AS1 Ensembl:ENSG00000240498 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1275411698 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_2252,RMVar_hsa_circ_35900,RMVar_hsa_circ_338946,RMVar_hsa_circ_357564,RMVar_hsa_circ_256183,RMVar_hsa_circ_117696,RMVar_hsa_circ_347125,RMVar_hsa_circ_58605,RMVar_hsa_circ_256185,RMVar_hsa_circ_347198,RMVar_hsa_circ_300534,RMVar_hsa_circ_28689,RMVar_hsa_circ_256190,RMVar_hsa_circ_256191 4864 RMVar_ID_4864 Human_SNP_ID_395018707 A-to-I Human chr9 - 26841962 26841962 26841962 TCTTTATTTTTAAATGTTTGGGCACCAAACCTAAAAGCAAAAGATTGACGAAGCATGTTTCTCTT TCTTTATTTTTAAATGTTTGGGCACCAAACCTGAAAGCAAAAGATTGACGAAGCATGTTTCTCTT T C CAAP1 Ensembl:ENSG00000120159 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs997686718 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7918318,Human_RBP_ID_9235585,Human_RBP_ID_24523222 4865 RMVar_ID_4865 Human_SNP_ID_395026543 A-to-I Human chr9 - 26870719 26870719 26870719 CCGTCTACTTGGGAGACTGAGGCAGGGGGATCACCTGAACCGGGGAGGCAGAGGTTGCAGTGAGC CCGTCTACTTGGGAGACTGAGGCAGGGGGATCTCCTGAACCGGGGAGGCAGAGGTTGCAGTGAGC T A CAAP1 Ensembl:ENSG00000120159 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569510165 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4404,RMVar_hsa_circ_281044,RMVar_hsa_circ_285523,RMVar_hsa_circ_58485,RMVar_hsa_circ_256221,RMVar_hsa_circ_256223 4866 RMVar_ID_4866 Human_SNP_ID_395026544 A-to-I Human chr9 - 26870719 26870719 26870719 CCGTCTACTTGGGAGACTGAGGCAGGGGGATCACCTGAACCGGGGAGGCAGAGGTTGCAGTGAGC CCGTCTACTTGGGAGACTGAGGCAGGGGGATCGCCTGAACCGGGGAGGCAGAGGTTGCAGTGAGC T C CAAP1 Ensembl:ENSG00000120159 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569510165 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4404,RMVar_hsa_circ_281044,RMVar_hsa_circ_285523,RMVar_hsa_circ_58485,RMVar_hsa_circ_256221,RMVar_hsa_circ_256223 4867 RMVar_ID_4867 Human_SNP_ID_395026558 A-to-I Human chr9 - 26870757 26870757 26870757 GAAAAATTAGCTGGGTGTGATGGCGCATGCCTATATTCCCGTCTACTTGGGAGACTGAGGCAGGG GAAAAATTAGCTGGGTGTGATGGCGCATGCCTGTATTCCCGTCTACTTGGGAGACTGAGGCAGGG T C CAAP1 Ensembl:ENSG00000120159 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215728924 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4404,RMVar_hsa_circ_281044,RMVar_hsa_circ_285523,RMVar_hsa_circ_58485,RMVar_hsa_circ_256221,RMVar_hsa_circ_256223 4868 RMVar_ID_4868 Human_SNP_ID_395026577 A-to-I Human chr9 - 26870825 26870824 26870825 ATCGCTTGAGGTCAGGAGTTTGAGACCACCCCAGCTAACATGGTGAAACCCCATCTCTTCTAAAA ATCGCTTGAGGTCAGGAGTTTGAGACCACCCC_GCTAACATGGTGAAACCCCATCTCTTCTAAAA CT C CAAP1 Ensembl:ENSG00000120159 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1181256158 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_4404,RMVar_hsa_circ_281044,RMVar_hsa_circ_285523,RMVar_hsa_circ_58485,RMVar_hsa_circ_256221,RMVar_hsa_circ_256223 4869 RMVar_ID_4869 Human_SNP_ID_395026578 A-to-I Human chr9 - 26870825 26870825 26870825 ATCGCTTGAGGTCAGGAGTTTGAGACCACCCCAGCTAACATGGTGAAACCCCATCTCTTCTAAAA ATCGCTTGAGGTCAGGAGTTTGAGACCACCCCCGCTAACATGGTGAAACCCCATCTCTTCTAAAA T G CAAP1 Ensembl:ENSG00000120159 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs566844412 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4404,RMVar_hsa_circ_281044,RMVar_hsa_circ_285523,RMVar_hsa_circ_58485,RMVar_hsa_circ_256221,RMVar_hsa_circ_256223 4870 RMVar_ID_4870 Human_SNP_ID_395044732 A-to-I Human chr9 - 26934640 26934640 26934640 CCCCGCCTCTACTAAAAATACAAAAATTATCCAGGTGTGGTGATGCCCACCAGTAATCCCAGCTA CCCCGCCTCTACTAAAAATACAAAAATTATCCCGGTGTGGTGATGCCCACCAGTAATCCCAGCTA T G PLAA Ensembl:ENSG00000137055 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1033853120 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38920,RMVar_hsa_circ_317623,RMVar_hsa_circ_256233,RMVar_hsa_circ_337062,RMVar_hsa_circ_256237,RMVar_hsa_circ_26298,RMVar_hsa_circ_286492,RMVar_hsa_circ_256239,RMVar_hsa_circ_329728,RMVar_hsa_circ_256241,RMVar_hsa_circ_295373 4871 RMVar_ID_4871 Human_SNP_ID_395065557 A-to-I Human chr9 + 27009106 27009106 27009106 AACAGATGACATTATCAAAAATATGTCTTTTGAAAACCAAGTCAAGTACCTAGAGATGAAAACCA AACAGATGACATTATCAAAAATATGTCTTTTGGAAACCAAGTCAAGTACCTAGAGATGAAAACCA A G IFT74 Ensembl:ENSG00000096872 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1210786711 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1036404,Human_Splice_Rec_1036405,Human_Splice_Rec_1036450,Human_Splice_Rec_1036451,Human_Splice_Rec_1036489,Human_Splice_Rec_1036526,Human_Splice_Rec_1036527,Human_Splice_Rec_1036572,Human_Splice_Rec_1036573 RMVar_hsa_circ_268438,RMVar_hsa_circ_284986,RMVar_hsa_circ_28643,RMVar_hsa_circ_337382,RMVar_hsa_circ_15306,RMVar_hsa_circ_358725,RMVar_hsa_circ_319358,RMVar_hsa_circ_256243,RMVar_hsa_circ_256244,RMVar_hsa_circ_256246,RMVar_hsa_circ_58247,RMVar_hsa_circ_324616,RMVar_hsa_circ_366701,RMVar_hsa_circ_256245,RMVar_hsa_circ_345244,RMVar_hsa_circ_318445,RMVar_hsa_circ_256250,RMVar_hsa_circ_272805,RMVar_hsa_circ_276458,RMVar_hsa_circ_256251,RMVar_hsa_circ_256248,RMVar_hsa_circ_256249,RMVar_hsa_circ_256247 4872 RMVar_ID_4872 Human_SNP_ID_395065558 A-to-I Human chr9 + 27009106 27009106 27009106 AACAGATGACATTATCAAAAATATGTCTTTTGAAAACCAAGTCAAGTACCTAGAGATGAAAACCA AACAGATGACATTATCAAAAATATGTCTTTTGTAAACCAAGTCAAGTACCTAGAGATGAAAACCA A T IFT74 Ensembl:ENSG00000096872 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1210786711 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1036404,Human_Splice_Rec_1036405,Human_Splice_Rec_1036450,Human_Splice_Rec_1036451,Human_Splice_Rec_1036489,Human_Splice_Rec_1036526,Human_Splice_Rec_1036527,Human_Splice_Rec_1036572,Human_Splice_Rec_1036573 RMVar_hsa_circ_268438,RMVar_hsa_circ_284986,RMVar_hsa_circ_28643,RMVar_hsa_circ_337382,RMVar_hsa_circ_15306,RMVar_hsa_circ_358725,RMVar_hsa_circ_319358,RMVar_hsa_circ_256243,RMVar_hsa_circ_256244,RMVar_hsa_circ_256246,RMVar_hsa_circ_58247,RMVar_hsa_circ_324616,RMVar_hsa_circ_366701,RMVar_hsa_circ_256245,RMVar_hsa_circ_345244,RMVar_hsa_circ_318445,RMVar_hsa_circ_256250,RMVar_hsa_circ_272805,RMVar_hsa_circ_276458,RMVar_hsa_circ_256251,RMVar_hsa_circ_256248,RMVar_hsa_circ_256249,RMVar_hsa_circ_256247 4873 RMVar_ID_4873 Human_SNP_ID_395073547 A-to-I Human chr9 + 27038551 27038551 27038551 CGCCTGTCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCCACCGCGCCCGGCCCAGGAA CGCCTGTCTTGGCCTCCCAAAGTGCTGGGATTGCAGGCGTGAGCCCACCGCGCCCGGCCCAGGAA A G IFT74 Ensembl:ENSG00000096872 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1274082477 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_319358,RMVar_hsa_circ_256244,RMVar_hsa_circ_256246,RMVar_hsa_circ_366701,RMVar_hsa_circ_256245,RMVar_hsa_circ_345244,RMVar_hsa_circ_272805,RMVar_hsa_circ_256247,RMVar_hsa_circ_53929,RMVar_hsa_circ_61426,RMVar_hsa_circ_66791 4874 RMVar_ID_4874 Human_SNP_ID_395082239 A-to-I Human chr9 + 27072225 27072225 27072225 GCCACCACGCCCAGGTAATTTTTTGTATTTTTAGTAGAGATGGAGTTTTGCCATGTTGGCCAGAC GCCACCACGCCCAGGTAATTTTTTGTATTTTTGGTAGAGATGGAGTTTTGCCATGTTGGCCAGAC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1265068765 Functional Loss SNV dbSNP153 33..33 33 - - - 4875 RMVar_ID_4875 Human_SNP_ID_395178997 A-to-I Human chr9 - 27415140 27415140 27415140 ATCTGGTTAGAGGGCTGGGCGTGGTGGCTCACACCTGTAATCCTAGCACTTTGGGAGGCTGAGGC ATCTGGTTAGAGGGCTGGGCGTGGTGGCTCACGCCTGTAATCCTAGCACTTTGGGAGGCTGAGGC T C MOB3B Ensembl:ENSG00000120162 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs938018637 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_339399 4876 RMVar_ID_4876 Human_SNP_ID_395196827 A-to-I Human chr9 - 27486896 27486896 27486896 GAACCCCTGGCCTCAAGTGATCCATCTGCCTCAGCCTCCCAAAGTGCTGGCATTACAAGCGTGAG GAACCCCTGGCCTCAAGTGATCCATCTGCCTCCGCCTCCCAAAGTGCTGGCATTACAAGCGTGAG T G MOB3B Ensembl:ENSG00000120162 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs533316034 Functional Loss SNV dbSNP153 33..33 33 - - - 4877 RMVar_ID_4877 Human_SNP_ID_395642554 A-to-I Human chr9 - 29144137 29144137 29144137 TATAGTAACCGAAACAGCACGGTACTGGTAAAAGAACAAACACATAAACCGATGGAACAGAGTAA TATAGTAACCGAAACAGCACGGTACTGGTAAACGAACAAACACATAAACCGATGGAACAGAGTAA T G lnc-LINGO2-5 RNACentral:URS00008BD0F6 lincRNA intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1483033605 Functional Loss SNV dbSNP153 33..33 33 - - - 4878 RMVar_ID_4878 Human_SNP_ID_395656699 A-to-I Human chr9 - 29198624 29198624 29198624 CAGTGTTTTAATTCAATGTATGTATGGCTTAAAAAATACGGAATGACACAAACTATGCTCTACTA CAGTGTTTTAATTCAATGTATGTATGGCTTAAGAAATACGGAATGACACAAACTATGCTCTACTA T C lnc-LINGO2-5,lnc-LINGO2-2,lnc-LINGO2-2:2,lnc-LINGO2-2:3 RNACentral:URS00008BD0F6,RNACentral:URS00008BAAF6,RNACentral:URS00008B65F1,RNACentral:URS00008B50FC lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs994798080 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3207280 4879 RMVar_ID_4879 Human_SNP_ID_395656705 A-to-I Human chr9 - 29198647 29198647 29198647 TTCACTCTGCTCAGCTAGGAATACAGTGTTTTAATTCAATGTATGTATGGCTTAAAAAATACGGA TTCACTCTGCTCAGCTAGGAATACAGTGTTTTGATTCAATGTATGTATGGCTTAAAAAATACGGA T C lnc-LINGO2-5,lnc-LINGO2-2,lnc-LINGO2-2:2,lnc-LINGO2-2:3 RNACentral:URS00008BD0F6,RNACentral:URS00008BAAF6,RNACentral:URS00008B65F1,RNACentral:URS00008B50FC lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs994606568 Functional Loss SNV dbSNP153 33..33 33 - - - 4880 RMVar_ID_4880 Human_SNP_ID_395822618 A-to-I Human chr9 - 29825554 29825554 29825554 TCTTATTCCTTGGAGCAGGAGAGATTACTCTTAGAATTGCAAATCTTGTAGTATGTCTATGGTAG TCTTATTCCTTGGAGCAGGAGAGATTACTCTTGGAATTGCAAATCTTGTAGTATGTCTATGGTAG T C ME2P1 Ensembl:ENSG00000230097 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1383418432 Functional Loss SNV dbSNP153 33..33 33 - - - 4881 RMVar_ID_4881 Human_SNP_ID_264107601 A-to-I Human chr6 - 277379 277379 277379 TAAGTAAAATAAGCTAGAACAAAAGGATAATTAGTGTATAATTCCACAGTAATTATCCAAGAGGT TAAGTAAAATAAGCTAGAACAAAAGGATAATTGGTGTATAATTCCACAGTAATTATCCAAGAGGT T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1481840563 Functional Loss SNV dbSNP153 33..33 33 - - - 4882 RMVar_ID_4882 Human_SNP_ID_264107612 A-to-I Human chr6 - 277439 277439 277439 AATTCAGCTTTAAAAAGTAATGAAGTTCTGATACTTAAATGAATCTTGAAAACATTATGCTAAGT AATTCAGCTTTAAAAAGTAATGAAGTTCTGATGCTTAAATGAATCTTGAAAACATTATGCTAAGT T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs923937396 Functional Loss SNV dbSNP153 33..33 33 - - - 4883 RMVar_ID_4883 Human_SNP_ID_264216552 A-to-I Human chr6 - 610135 610135 610135 AAACTAGAAGCAGATGGAACGGAAAAAGTAGAAGGATCCATGACGCAGAAACTGGAGAATGTTCT AAACTAGAAGCAGATGGAACGGAAAAAGTAGATGGATCCATGACGCAGAAACTGGAGAATGTTCT T A EXOC2 Ensembl:ENSG00000112685 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1293660236 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2024683,Human_RBP_ID_5622343,Human_RBP_ID_15862495 Human_Splice_Rec_732746,Human_Splice_Rec_732747 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_23168,RMVar_hsa_circ_236869,RMVar_hsa_circ_97473,RMVar_hsa_circ_122135,RMVar_hsa_circ_376358,RMVar_hsa_circ_236870,RMVar_hsa_circ_236868,RMVar_hsa_circ_290393,RMVar_hsa_circ_348999,RMVar_hsa_circ_236872 4884 RMVar_ID_4884 Human_SNP_ID_264393427 A-to-I Human chr6 - 1305974 1305974 1305974 CTCTATGTTGCCCAGACTGGTCTCAAACTTCTAGGCTCAAGCTATCCTTCTATCTCAGCCTCTTG CTCTATGTTGCCCAGACTGGTCTCAAACTTCTGGGCTCAAGCTATCCTTCTATCTCAGCCTCTTG T C LINC01394,LINC01394:2,LINC01394:3,LINC01394:4 RNACentral:URS00008BFF5A,RNACentral:URS00008C018F,RNACentral:URS00008B5069,RNACentral:URS00008B7B78 lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1183899393 Functional Loss SNV dbSNP153 33..33 33 - - - 4885 RMVar_ID_4885 Human_SNP_ID_264485116 A-to-I Human chr6 - 1648091 1648091 1648091 TAGGCGAGGATGTCCTCACTCTCTCAAGAGATATATTTTGAGTCCTCACTATAGGCAAATAGGTA TAGGCGAGGATGTCCTCACTCTCTCAAGAGATGTATTTTGAGTCCTCACTATAGGCAAATAGGTA T C GMDS Ensembl:ENSG00000112699 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1369307255 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22728288 4886 RMVar_ID_4886 Human_SNP_ID_264584438 A-to-I Human chr6 - 2046156 2046156 2046156 CAGGCTGGAGTGCAGTGGCATGATCTTGGCTCACTGTAGACTCTGCTCCCTGGGCTCAAGCGATC CAGGCTGGAGTGCAGTGGCATGATCTTGGCTCGCTGTAGACTCTGCTCCCTGGGCTCAAGCGATC T C GMDS Ensembl:ENSG00000112699 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559093595 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 4887 RMVar_ID_4887 Human_SNP_ID_264592483 A-to-I Human chr6 - 2075088 2075088 2075088 ACAGCCAAAGAAATCCTGAGCAAAAGGAATAAAGCTGGAAGCATCACACTCTCTGACCTCAAAAT ACAGCCAAAGAAATCCTGAGCAAAAGGAATAAGGCTGGAAGCATCACACTCTCTGACCTCAAAAT T C GMDS Ensembl:ENSG00000112699 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1399939750 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 4888 RMVar_ID_4888 Human_SNP_ID_264639814 A-to-I Human chr6 + 2269790 2269790 2269790 GGGATCCTCCTGCCTCAGCCTCCCAAGTAGCTAGGACTACAGGTATGTGCCACCACTCCCAACTA GGGATCCTCCTGCCTCAGCCTCCCAAGTAGCTCGGACTACAGGTATGTGCCACCACTCCCAACTA A C GMDS-DT Ensembl:ENSG00000250903 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs773795889 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_733028,Human_Splice_Rec_733029,Human_Splice_Rec_733046,Human_Splice_Rec_733047,Human_Splice_Rec_733074,Human_Splice_Rec_733075,Human_Splice_Rec_733088,Human_Splice_Rec_733089,Human_Splice_Rec_733100,Human_Splice_Rec_733101,Human_Splice_Rec_733154,Human_Splice_Rec_733160,Human_Splice_Rec_733161,Human_Splice_Rec_733168,Human_Splice_Rec_733169 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 4889 RMVar_ID_4889 Human_SNP_ID_264639815 A-to-I Human chr6 + 2269790 2269790 2269790 GGGATCCTCCTGCCTCAGCCTCCCAAGTAGCTAGGACTACAGGTATGTGCCACCACTCCCAACTA GGGATCCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGTATGTGCCACCACTCCCAACTA A G GMDS-DT Ensembl:ENSG00000250903 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs773795889 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_733028,Human_Splice_Rec_733029,Human_Splice_Rec_733046,Human_Splice_Rec_733047,Human_Splice_Rec_733074,Human_Splice_Rec_733075,Human_Splice_Rec_733088,Human_Splice_Rec_733089,Human_Splice_Rec_733100,Human_Splice_Rec_733101,Human_Splice_Rec_733154,Human_Splice_Rec_733160,Human_Splice_Rec_733161,Human_Splice_Rec_733168,Human_Splice_Rec_733169 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 4890 RMVar_ID_4890 Human_SNP_ID_264639824 A-to-I Human chr6 + 2269844 2269844 2269844 ACTCCCAACTAATTTTTTTATTTTTTGTAGAGACGAGATCTAACTTTGTTGCCCAGGCTGGTATT ACTCCCAACTAATTTTTTTATTTTTTGTAGAGCCGAGATCTAACTTTGTTGCCCAGGCTGGTATT A C GMDS-DT Ensembl:ENSG00000250903 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1243404236 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_354242,RMVar_hsa_circ_271586,RMVar_hsa_circ_236889,RMVar_hsa_circ_236890,RMVar_hsa_circ_236891 4891 RMVar_ID_4891 Human_SNP_ID_264640647 A-to-I Human chr6 + 2273754 2273754 2273754 GCAGTGATTCACACCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCTGGAGGATTGCTTGAGCCTA GCAGTGATTCACACCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCTGGAGGATTGCTTGAGCCTA A G GMDS-DT Ensembl:ENSG00000250903 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1396291886 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_354242,RMVar_hsa_circ_236890,RMVar_hsa_circ_236891 4892 RMVar_ID_4892 Human_SNP_ID_264659888 A-to-I Human chr6 + 2349944 2349944 2349944 AAAATTACCTGGGCATGGTGGCATACACCTGTAGTCCAAGCAACTTTGGAGGCTGAGGTGGGAGG AAAATTACCTGGGCATGGTGGCATACACCTGTTGTCCAAGCAACTTTGGAGGCTGAGGTGGGAGG A T GMDS-DT Ensembl:ENSG00000250903 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1249558705 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17576199 RMVar_hsa_circ_354242,RMVar_hsa_circ_32701,RMVar_hsa_circ_236891,RMVar_hsa_circ_236892 4893 RMVar_ID_4893 Human_SNP_ID_264787829 A-to-I Human chr6 - 2860098 2860098 2860098 GCAAGCTGAGGGAGTGGGCTCCAGCCTTGGCCAGCCCAGAAAGGGGCTCCCACAGTGCAGTGGGG GCAAGCTGAGGGAGTGGGCTCCAGCCTTGGCCCGCCCAGAAAGGGGCTCCCACAGTGCAGTGGGG T G SERPINB9P1 Ensembl:ENSG00000230438 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1208966002 Functional Loss SNV dbSNP153 33..33 33 - - - 4894 RMVar_ID_4894 Human_SNP_ID_264787898 A-to-I Human chr6 - 2860183 2860183 2860183 CCACGTCCACCCGGAACTCCAGCTGGCCAGCAAGCGCTGCACGCAGCCCCGGTTCCCGCTCGTGC CCACGTCCACCCGGAACTCCAGCTGGCCAGCAGGCGCTGCACGCAGCCCCGGTTCCCGCTCGTGC T C SERPINB9P1 Ensembl:ENSG00000230438 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs570131328 Functional Loss SNV dbSNP153 33..33 33 - - - 4895 RMVar_ID_4895 Human_SNP_ID_264816469 A-to-I Human chr6 - 2948533 2948533 2948533 CCTGGGCATGACTGATGCCTTCGAGCTGGGCAAGGCAGACTTCTCTGGAATGTCCCAGACAGACC CCTGGGCATGACTGATGCCTTCGAGCTGGGCACGGCAGACTTCTCTGGAATGTCCCAGACAGACC T G SERPINB6 Ensembl:ENSG00000124570 Protein coding exon GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1028904180 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_660399,Human_RBP_ID_5121818,Human_RBP_ID_24155548 Human_miRNA_ID_2455152,Human_miRNA_ID_2824392,Human_miRNA_ID_2858363 RMVar_hsa_circ_83951,RMVar_hsa_circ_109018,RMVar_hsa_circ_119768,RMVar_hsa_circ_121953,RMVar_hsa_circ_91306,RMVar_hsa_circ_236916,RMVar_hsa_circ_236918,RMVar_hsa_circ_236920,RMVar_hsa_circ_81860,RMVar_hsa_circ_236919,RMVar_hsa_circ_236917,RMVar_hsa_circ_236915 4896 RMVar_ID_4896 Human_SNP_ID_264820587 A-to-I Human chr6 - 2964929 2964929 2964929 AGGAGGCTGACGCTAAAGGATTGCTTGAGGCCAGGAGTTCGAGGCTGCAGTGGGCCGTGATCATG AGGAGGCTGACGCTAAAGGATTGCTTGAGGCCCGGAGTTCGAGGCTGCAGTGGGCCGTGATCATG T G SERPINB6 Ensembl:ENSG00000124570 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1227161574 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83951,RMVar_hsa_circ_236920 4897 RMVar_ID_4897 Human_SNP_ID_264833789 A-to-I Human chr6 - 3016309 3016309 3016309 CTCCTGCCTCGGCCTCCCAAGTAGCTGGGACTACAGGCGCCTACCACCATGCCCGGCTAATTTTT CTCCTGCCTCGGCCTCCCAAGTAGCTGGGACTTCAGGCGCCTACCACCATGCCCGGCTAATTTTT T A lnc-SERPINB6-1,lnc-SERPINB6-1:2 RNACentral:URS00008BF125,RNACentral:URS00008BE890 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs961843756 Functional Loss SNV dbSNP153 33..33 33 - - - 4898 RMVar_ID_4898 Human_SNP_ID_264833797 A-to-I Human chr6 + 3016337 3016337 3016337 CCTGTAGTCCCAGCTACTTGGGAGGCCGAGGCAGGAGACTGGTTTGAACCTGGGAGGTGGAGGTT CCTGTAGTCCCAGCTACTTGGGAGGCCGAGGCGGGAGACTGGTTTGAACCTGGGAGGTGGAGGTT A G NQO2 Ensembl:ENSG00000124588 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1279318438 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102215,RMVar_hsa_circ_236926,RMVar_hsa_circ_368402,RMVar_hsa_circ_80995,RMVar_hsa_circ_236929,RMVar_hsa_circ_77236,RMVar_hsa_circ_119992,RMVar_hsa_circ_92352,RMVar_hsa_circ_325697,RMVar_hsa_circ_236931,RMVar_hsa_circ_236932,RMVar_hsa_circ_96997,RMVar_hsa_circ_236937,RMVar_hsa_circ_236938,RMVar_hsa_circ_77590,RMVar_hsa_circ_236939,RMVar_hsa_circ_236940 4899 RMVar_ID_4899 Human_SNP_ID_264834380 A-to-I Human chr6 + 3018394 3018394 3018394 GAGTGTGGTGGCGGACACCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGCAGAATCGCTTGAA GAGTGTGGTGGCGGACACCTGTAGTCCCAGCTGCTTGGGAGGCTGAGGCAGCAGAATCGCTTGAA A G NQO2 Ensembl:ENSG00000124588 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1406562024 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80995,RMVar_hsa_circ_236929,RMVar_hsa_circ_77236,RMVar_hsa_circ_119992,RMVar_hsa_circ_236931,RMVar_hsa_circ_96997,RMVar_hsa_circ_236938,RMVar_hsa_circ_77590,RMVar_hsa_circ_236939,RMVar_hsa_circ_114497,RMVar_hsa_circ_236940,RMVar_hsa_circ_236942 4900 RMVar_ID_4900 Human_SNP_ID_264835031 A-to-I Human chr6 + 3021051 3021051 3021051 AGCTGGGTGCAGTGGCATGATCATACCTCACTAGGCTCAAGTGATCCTCCTGCCTCAGCATCCCT AGCTGGGTGCAGTGGCATGATCATACCTCACTGGGCTCAAGTGATCCTCCTGCCTCAGCATCCCT A G NQO2 Ensembl:ENSG00000124588 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs931888397 Functional Loss SNV dbSNP153 33..33 33 - - - 4901 RMVar_ID_4901 Human_SNP_ID_264835046 A-to-I Human chr6 + 3021084 3021084 3021084 GGCTCAAGTGATCCTCCTGCCTCAGCATCCCTAGTAACTAGGACTACAGGCACATGCTACCACGC GGCTCAAGTGATCCTCCTGCCTCAGCATCCCTCGTAACTAGGACTACAGGCACATGCTACCACGC A C NQO2 Ensembl:ENSG00000124588 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs927526357 Functional Loss SNV dbSNP153 33..33 33 - - - 4902 RMVar_ID_4902 Human_SNP_ID_264835047 A-to-I Human chr6 + 3021087 3021087 3021087 TCAAGTGATCCTCCTGCCTCAGCATCCCTAGTAACTAGGACTACAGGCACATGCTACCACGCCTG TCAAGTGATCCTCCTGCCTCAGCATCCCTAGTGACTAGGACTACAGGCACATGCTACCACGCCTG A G NQO2 Ensembl:ENSG00000124588 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs750059016 Functional Loss SNV dbSNP153 33..33 33 - - - 4903 RMVar_ID_4903 Human_SNP_ID_264835054 A-to-I Human chr6 + 3021123 3021123 3021123 AGGACTACAGGCACATGCTACCACGCCTGGCTAATTATTTTAATTTTTGGTAGAGACAGGATCTC AGGACTACAGGCACATGCTACCACGCCTGGCTCATTATTTTAATTTTTGGTAGAGACAGGATCTC A C NQO2 Ensembl:ENSG00000124588 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1453219769 Functional Loss SNV dbSNP153 33..33 33 - - - 4904 RMVar_ID_4904 Human_SNP_ID_264835271 A-to-I Human chr6 - 3021992 3021992 3021992 CTCCTGCCTCAGCCTCCCGGGTAGCTGGGACTACAGGCGCCCGCCACCAGACCCGGCTAAATATT CTCCTGCCTCAGCCTCCCGGGTAGCTGGGACTGCAGGCGCCCGCCACCAGACCCGGCTAAATATT T C lnc-SERPINB6-1,lnc-SERPINB6-1:2 RNACentral:URS00008BE890,RNACentral:URS00008B45E2 lincRNA,lincRNA intron,exon GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1021617558 Functional Loss SNV dbSNP153 33..33 33 - - - 4905 RMVar_ID_4905 Human_SNP_ID_264835351 A-to-I Human chr6 + 3022233 3022233 3022233 GAGGCCAGGAGTTCAAGACCAGCTTGGGCAACATAATGAGACCCATCTCTACAAAAAATTTAAAA GAGGCCAGGAGTTCAAGACCAGCTTGGGCAACCTAATGAGACCCATCTCTACAAAAAATTTAAAA A C NQO2 Ensembl:ENSG00000124588 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs556579849 Functional Loss SNV dbSNP153 33..33 33 - - - 4906 RMVar_ID_4906 Human_SNP_ID_264835363 A-to-I Human chr6 + 3022283 3022283 3022283 ACAAAAAATTTAAAAATATACATTAGTTAGGCATGGTGGCACGCACCTGTAATTCCAGCTACTCA ACAAAAAATTTAAAAATATACATTAGTTAGGCGTGGTGGCACGCACCTGTAATTCCAGCTACTCA A G NQO2 Ensembl:ENSG00000124588 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1050550818 Functional Loss SNV dbSNP153 33..33 33 - - - 4907 RMVar_ID_4907 Human_SNP_ID_264835364 A-to-I Human chr6 + 3022283 3022283 3022283 ACAAAAAATTTAAAAATATACATTAGTTAGGCATGGTGGCACGCACCTGTAATTCCAGCTACTCA ACAAAAAATTTAAAAATATACATTAGTTAGGCTTGGTGGCACGCACCTGTAATTCCAGCTACTCA A T NQO2 Ensembl:ENSG00000124588 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1050550818 Functional Loss SNV dbSNP153 33..33 33 - - - 4908 RMVar_ID_4908 Human_SNP_ID_264835368 A-to-I Human chr6 - 3022310 3022310 3022310 TCACGTGACCCTCTTGCTTCAGCCTCCTGAGTAGCTGGAATTACAGGTGCGTGCCACCATGCCTA TCACGTGACCCTCTTGCTTCAGCCTCCTGAGTGGCTGGAATTACAGGTGCGTGCCACCATGCCTA T C lnc-SERPINB6-1,lnc-SERPINB6-1:2 RNACentral:URS00008BE890,RNACentral:URS00008B45E2 lincRNA,lincRNA intron,exon GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1442604908 Functional Loss SNV dbSNP153 33..33 33 - - - 4909 RMVar_ID_4909 Human_SNP_ID_264835371 A-to-I Human chr6 + 3022315 3022315 3022315 ATGGTGGCACGCACCTGTAATTCCAGCTACTCAGGAGGCTGAAGCAAGAGGGTCACGTGAGTCCA ATGGTGGCACGCACCTGTAATTCCAGCTACTCGGGAGGCTGAAGCAAGAGGGTCACGTGAGTCCA A G NQO2 Ensembl:ENSG00000124588 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1325634111 Functional Loss SNV dbSNP153 33..33 33 - - - 4910 RMVar_ID_4910 Human_SNP_ID_264835408 A-to-I Human chr6 - 3022487 3022487 3022487 CCAGGCTGGCCTCAAACTGCTGAACTCAAGCAATCTGCCCATCTTAGCCTCCAAAAATGCTGGGA CCAGGCTGGCCTCAAACTGCTGAACTCAAGCAGTCTGCCCATCTTAGCCTCCAAAAATGCTGGGA T C lnc-SERPINB6-1,lnc-SERPINB6-1:2,lnc-SERPINB6-1:3 RNACentral:URS00008B54B8,RNACentral:URS00008BE890,RNACentral:URS00008B45E2 lincRNA,lincRNA,lincRNA exon,intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs915092361 Functional Loss SNV dbSNP153 33..33 33 - - - 4911 RMVar_ID_4911 Human_SNP_ID_264848591 A-to-I Human chr6 + 3070603 3070603 3070603 GGGATTGTAGGCATGCACTACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGGCTTCA GGGATTGTAGGCATGCACTACCATGCCTGGCTGATTTTTGTATTTTTAGTAGAGACAGGGCTTCA A G RIPK1 Ensembl:ENSG00000137275 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1337325969 Functional Loss SNV dbSNP153 33..33 33 - - - 4912 RMVar_ID_4912 Human_SNP_ID_264864818 A-to-I Human chr6 + 3132711 3132711 3132711 AAACGTAGTCAGGTGTGGTGGCATGTGCCTGTAGTCCCAGCCATTTGGGAGGCTGAGGTGGAGGA AAACGTAGTCAGGTGTGGTGGCATGTGCCTGTTGTCCCAGCCATTTGGGAGGCTGAGGTGGAGGA A T BPHL Ensembl:ENSG00000137274 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1278042978 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_338994,RMVar_hsa_circ_21265,RMVar_hsa_circ_357032 4913 RMVar_ID_4913 Human_SNP_ID_264910149 A-to-I Human chr6 + 3286286 3286286 3286286 AAGCCCAGCTAATTATTTTTTGTATATTTAGTAGAGATGGGGTTTCACTACATTGGTCAGGCTGG AAGCCCAGCTAATTATTTTTTGTATATTTAGTGGAGATGGGGTTTCACTACATTGGTCAGGCTGG A G PSMG4 Ensembl:ENSG00000180822 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1425422530 Functional Loss SNV dbSNP153 33..33 33 - - - 4914 RMVar_ID_4914 Human_SNP_ID_265089639 A-to-I Human chr6 - 3969274 3969274 3969274 GAACTCCTGACCTCAGGTGAGCCACCTGTCTCAGCATCCCAAAGTGCTGGGATTACAGACGTGAG GAACTCCTGACCTCAGGTGAGCCACCTGTCTCTGCATCCCAAAGTGCTGGGATTACAGACGTGAG T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1326338506 Functional Loss SNV dbSNP153 33..33 33 - - - 4915 RMVar_ID_4915 Human_SNP_ID_265099698 A-to-I Human chr6 - 4010807 4010807 4010807 ATGGTGCAGCATGCCTATAGCCCCAGCTACTCAGGAGGCTGAAGTGGGAGGATCACTTGAGACCA ATGGTGCAGCATGCCTATAGCCCCAGCTACTCGGGAGGCTGAAGTGGGAGGATCACTTGAGACCA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs915836770 Functional Loss SNV dbSNP153 33..33 33 - - - 4916 RMVar_ID_4916 Human_SNP_ID_265106493 A-to-I Human chr6 + 4035922 4035922 4035922 GGGAGACAGAGGTTGCAGTGAGCCGAGGTCACACCATTGCACTACAGCCTGTGCAACAAGAGCAA GGGAGACAGAGGTTGCAGTGAGCCGAGGTCACGCCATTGCACTACAGCCTGTGCAACAAGAGCAA A G PRPF4B Ensembl:ENSG00000112739 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1013287907 Functional Loss SNV dbSNP153 33..33 33 - - - 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_121680,RMVar_hsa_circ_236972,RMVar_hsa_circ_236969,RMVar_hsa_circ_56044,RMVar_hsa_circ_236970 4917 RMVar_ID_4917 Human_SNP_ID_265106602 A-to-I Human chr6 + 4036301 4036301 4036301 TGGAGTGCAGTGGCATGATCTCTGCTCACTGCAACCTCTGCCTCCCAGGCTTACACAATCCTCCC TGGAGTGCAGTGGCATGATCTCTGCTCACTGCCACCTCTGCCTCCCAGGCTTACACAATCCTCCC A C PRPF4B Ensembl:ENSG00000112739 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1200710210 Functional Loss SNV dbSNP153 33..33 33 - - - 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_121680,RMVar_hsa_circ_236972,RMVar_hsa_circ_236969,RMVar_hsa_circ_56044,RMVar_hsa_circ_236970 4918 RMVar_ID_4918 Human_SNP_ID_265106630 A-to-I Human chr6 + 4036405 4036405 4036405 CACCACACTTGGCTAATTTTGATATTTTTTGTAGAGATAGGGTTTCGCCATGTTACCCAGGCTGG CACCACACTTGGCTAATTTTGATATTTTTTGTGGAGATAGGGTTTCGCCATGTTACCCAGGCTGG A G PRPF4B Ensembl:ENSG00000112739 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1487056154 Functional Loss SNV dbSNP153 33..33 33 - - - 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_121680,RMVar_hsa_circ_236972,RMVar_hsa_circ_236969,RMVar_hsa_circ_56044,RMVar_hsa_circ_236970 4919 RMVar_ID_4919 Human_SNP_ID_265296909 A-to-I Human chr6 + 4787798 4787798 4787798 TTTTTTTTTTTTTTTTTTTTTTTGGGAGACAGAGTCTCGCTCTGTTGCCCAGGCTGGAGGGCAAT TTTTTTTTTTTTTTTTTTTTTTTGGGAGACAGGGTCTCGCTCTGTTGCCCAGGCTGGAGGGCAAT A G CDYL Ensembl:ENSG00000153046 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1387097925 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99483,RMVar_hsa_circ_75910,RMVar_hsa_circ_236982,RMVar_hsa_circ_236983 4920 RMVar_ID_4920 Human_SNP_ID_265297043 A-to-I Human chr6 + 4788261 4788261 4788261 CCTGTAATCCCAGAACTTCGGGAGGCCAAGGCAGGAGGATCACTTGAGGCCAGGAGTTCAAGACC CCTGTAATCCCAGAACTTCGGGAGGCCAAGGCGGGAGGATCACTTGAGGCCAGGAGTTCAAGACC A G CDYL Ensembl:ENSG00000153046 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs940428603 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99483,RMVar_hsa_circ_75910,RMVar_hsa_circ_236982,RMVar_hsa_circ_236983 4921 RMVar_ID_4921 Human_SNP_ID_265303640 A-to-I Human chr6 + 4813973 4813973 4813973 TTTTTTTTTTTTTTTTGTAGAAACAGGATTTTACCACATTGCCTAGGTTGGTCTTGAACTCCAGC TTTTTTTTTTTTTTTTGTAGAAACAGGATTTTTCCACATTGCCTAGGTTGGTCTTGAACTCCAGC A T CDYL Ensembl:ENSG00000153046 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1289006250 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15842232 RMVar_hsa_circ_99483,RMVar_hsa_circ_75910,RMVar_hsa_circ_236982,RMVar_hsa_circ_236983 4922 RMVar_ID_4922 Human_SNP_ID_265305672 A-to-I Human chr6 + 4821501 4821501 4821501 CATGCCTGTAATCCCGGCACTTTGGGGGGCCGAAGCGGGCGGATCACTTGAGCTCAGGAGTTTGA CATGCCTGTAATCCCGGCACTTTGGGGGGCCGGAGCGGGCGGATCACTTGAGCTCAGGAGTTTGA A G CDYL Ensembl:ENSG00000153046 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1395005294 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99483,RMVar_hsa_circ_75910,RMVar_hsa_circ_236982,RMVar_hsa_circ_236983 4923 RMVar_ID_4923 Human_SNP_ID_265342013 A-to-I Human chr6 + 4952965 4952965 4952965 TATTTTTGTATTTTCAGTAGACACGGAGTCTCACCACGTTGGCCAGGCTGGTCTCGAACTCCTGA TATTTTTGTATTTTCAGTAGACACGGAGTCTCGCCACGTTGGCCAGGCTGGTCTCGAACTCCTGA A G CDYL Ensembl:ENSG00000153046 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968621219 Functional Loss SNV dbSNP153 33..33 33 - - - 4924 RMVar_ID_4924 Human_SNP_ID_265342023 A-to-I Human chr6 + 4953012 4953009 4953013 CTGGTCTCGAACTCCTGACCTCAAGTTGATCCACCCACCTCAGCCTCCCAAAGTGCTGGAATTAC CTGGTCTCGAACTCCTGACCTCAAGTTGAT____CCACCTCAGCCTCCCAAAGTGCTGGAATTAC TCCAC T CDYL Ensembl:ENSG00000153046 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1409451889 Functional Loss DEL dbSNP153 31..34 33 - - - 4925 RMVar_ID_4925 Human_SNP_ID_265342076 A-to-I Human chr6 + 4953205 4953205 4953205 CAGGAGTTGGAGACCAGCCTGGCCAACATGGCAAAACCCCGTCTGTACTAAAAATCCAAAAGTTA CAGGAGTTGGAGACCAGCCTGGCCAACATGGCGAAACCCCGTCTGTACTAAAAATCCAAAAGTTA A G CDYL Ensembl:ENSG00000153046 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs894440579 Functional Loss SNV dbSNP153 33..33 33 - - - 4926 RMVar_ID_4926 Human_SNP_ID_265342084 A-to-I Human chr6 + 4953222 4953222 4953222 CCTGGCCAACATGGCAAAACCCCGTCTGTACTAAAAATCCAAAAGTTAGCCAGGCTTGGTGGTGC CCTGGCCAACATGGCAAAACCCCGTCTGTACTGAAAATCCAAAAGTTAGCCAGGCTTGGTGGTGC A G CDYL Ensembl:ENSG00000153046 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1023935744 Functional Loss SNV dbSNP153 33..33 33 - - - 4927 RMVar_ID_4927 Human_SNP_ID_265342096 A-to-I Human chr6 + 4953255 4953255 4953255 AAAATCCAAAAGTTAGCCAGGCTTGGTGGTGCACGCCTGTAATCCCAACTACTCGAGAGGCTGAG AAAATCCAAAAGTTAGCCAGGCTTGGTGGTGCTCGCCTGTAATCCCAACTACTCGAGAGGCTGAG A T CDYL Ensembl:ENSG00000153046 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1030834513 Functional Loss SNV dbSNP153 33..33 33 - - - 4928 RMVar_ID_4928 Human_SNP_ID_265342100 A-to-I Human chr6 + 4953269 4953269 4953269 AGCCAGGCTTGGTGGTGCACGCCTGTAATCCCAACTACTCGAGAGGCTGAGGTGAGAGAATCGCT AGCCAGGCTTGGTGGTGCACGCCTGTAATCCCGACTACTCGAGAGGCTGAGGTGAGAGAATCGCT A G CDYL Ensembl:ENSG00000153046 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs546639803 Functional Loss SNV dbSNP153 33..33 33 - - - 4929 RMVar_ID_4929 Human_SNP_ID_265380575 A-to-I Human chr6 - 5104377 5104377 5104377 CTAGCTACTCTGGAGCCTGAGGTGGGAGGATCACTTGAGCCTGGAAGGCGGAGGTTGCAGTGAGC CTAGCTACTCTGGAGCCTGAGGTGGGAGGATCGCTTGAGCCTGGAAGGCGGAGGTTGCAGTGAGC T C LYRM4 Ensembl:ENSG00000214113 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1561797733 Functional Loss SNV dbSNP153 33..33 33 - - - 4930 RMVar_ID_4930 Human_SNP_ID_265393254 A-to-I Human chr6 - 5154633 5154633 5154633 TTTGTGTGTTTTTAGTACAGACAGGGTTTCACAGTGTTCGTCAGGATGGTCTCGATCTCCTGACC TTTGTGTGTTTTTAGTACAGACAGGGTTTCACTGTGTTCGTCAGGATGGTCTCGATCTCCTGACC T A LYRM4 Ensembl:ENSG00000214113 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs966761859 Functional Loss SNV dbSNP153 33..33 33 - - - 4931 RMVar_ID_4931 Human_SNP_ID_265393255 A-to-I Human chr6 - 5154633 5154633 5154633 TTTGTGTGTTTTTAGTACAGACAGGGTTTCACAGTGTTCGTCAGGATGGTCTCGATCTCCTGACC TTTGTGTGTTTTTAGTACAGACAGGGTTTCACCGTGTTCGTCAGGATGGTCTCGATCTCCTGACC T G LYRM4 Ensembl:ENSG00000214113 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs966761859 Functional Loss SNV dbSNP153 33..33 33 - - - 4932 RMVar_ID_4932 Human_SNP_ID_265401435 A-to-I Human chr6 - 5188104 5188104 5188104 CCTCAAGTAGTCCTCCCACCTCAGCCTCCCAAAGTGTTGGGATTACAGGTGTGAGCCACCATGCG CCTCAAGTAGTCCTCCCACCTCAGCCTCCCAATGTGTTGGGATTACAGGTGTGAGCCACCATGCG T A LYRM4 Ensembl:ENSG00000214113 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1409595533 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21947530 4933 RMVar_ID_4933 Human_SNP_ID_265417815 A-to-I Human chr6 - 5256086 5256086 5256086 CTAATTTTCTCACCTTAAACTAGGATTTCTCAATCTTGGCATGACCAACCTTTTGGGCCAGCTAA CTAATTTTCTCACCTTAAACTAGGATTTCTCAGTCTTGGCATGACCAACCTTTTGGGCCAGCTAA T C LYRM4 Ensembl:ENSG00000214113 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1266464039 Functional Loss SNV dbSNP153 33..33 33 - - - 4934 RMVar_ID_4934 Human_SNP_ID_265417837 A-to-I Human chr6 - 5256152 5256152 5256152 TCTTCTTGGCTCTTCTTCAGCCAACTCCTTCAATTCTGATGTTCCCTAGAATAGCATCCGTAGCC TCTTCTTGGCTCTTCTTCAGCCAACTCCTTCAGTTCTGATGTTCCCTAGAATAGCATCCGTAGCC T C LYRM4 Ensembl:ENSG00000214113 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1482291845 Functional Loss SNV dbSNP153 33..33 33 - - - 4935 RMVar_ID_4935 Human_SNP_ID_265417838 A-to-I Human chr6 - 5256153 5256153 5256153 GTCTTCTTGGCTCTTCTTCAGCCAACTCCTTCAATTCTGATGTTCCCTAGAATAGCATCCGTAGC GTCTTCTTGGCTCTTCTTCAGCCAACTCCTTCGATTCTGATGTTCCCTAGAATAGCATCCGTAGC T C LYRM4 Ensembl:ENSG00000214113 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs71557552 Functional Loss SNV dbSNP153 33..33 33 - - - 4936 RMVar_ID_4936 Human_SNP_ID_265420542 A-to-I Human chr6 + 5265002 5265002 5265002 GTTTTTTTTTTTTTTTGTAGAGATGAGATTTCACTATGATGTCCAGGGTGGTCTCAAACTCCTCA GTTTTTTTTTTTTTTTGTAGAGATGAGATTTCGCTATGATGTCCAGGGTGGTCTCAAACTCCTCA A G FARS2 Ensembl:ENSG00000145982 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1279089085 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17576206 RMVar_hsa_circ_92755,RMVar_hsa_circ_110533,RMVar_hsa_circ_236996,RMVar_hsa_circ_236997 4937 RMVar_ID_4937 Human_SNP_ID_265421216 A-to-I Human chr6 + 5267711 5267711 5267711 GGGAGGTGGAGCTTGTAGTGAGCTGAGATCGCACCACTGCACTCCAGCTTGGGAGACACAGCGAG GGGAGGTGGAGCTTGTAGTGAGCTGAGATCGCGCCACTGCACTCCAGCTTGGGAGACACAGCGAG A G FARS2 Ensembl:ENSG00000145982 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs572704366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26048333 RMVar_hsa_circ_92755,RMVar_hsa_circ_110533,RMVar_hsa_circ_236996,RMVar_hsa_circ_236997 4938 RMVar_ID_4938 Human_SNP_ID_265428250 A-to-I Human chr6 + 5296211 5296211 5296211 TCGCCTGGGCTGGAGTGCAGTGGTGGGATCTCAGCTCACTGCAAGCTCCGCCTCCCGGGTTCACA TCGCCTGGGCTGGAGTGCAGTGGTGGGATCTCGGCTCACTGCAAGCTCCGCCTCCCGGGTTCACA A G FARS2 Ensembl:ENSG00000145982 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs961206296 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92755,RMVar_hsa_circ_110533,RMVar_hsa_circ_236996,RMVar_hsa_circ_236997 4939 RMVar_ID_4939 Human_SNP_ID_265438761 A-to-I Human chr6 + 5341037 5341037 5341037 AGGCATGGTGACGTGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAA AGGCATGGTGACGTGCGCCTGTAATCCCAGCTTCTCAGGAGGCTGAGGCAGGAGAATCGCTTGAA A T FARS2 Ensembl:ENSG00000145982 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1295143601 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92755,RMVar_hsa_circ_110533,RMVar_hsa_circ_236996,RMVar_hsa_circ_236997 4940 RMVar_ID_4940 Human_SNP_ID_265507299 A-to-I Human chr6 + 5621226 5621226 5621226 TTCCTACCTTAGTCTCCCAAGTAGCTAGGACTACAGGCATAGGCCACCACACTTGGCTAACTTTT TTCCTACCTTAGTCTCCCAAGTAGCTAGGACTGCAGGCATAGGCCACCACACTTGGCTAACTTTT A G FARS2 Ensembl:ENSG00000145982 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs556738065 Functional Loss SNV dbSNP153 33..33 33 - - - 4941 RMVar_ID_4941 Human_SNP_ID_265514270 A-to-I Human chr6 + 5650451 5650451 5650451 TCAAGGAGATTTACCAAGCACCATTATAATTTAAAAAATTAACCCTCTAACAAATTGCGGCATGG TCAAGGAGATTTACCAAGCACCATTATAATTTTAAAAATTAACCCTCTAACAAATTGCGGCATGG A T FARS2 Ensembl:ENSG00000145982 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1010208680 Functional Loss SNV dbSNP153 33..33 33 - - - 4942 RMVar_ID_4942 Human_SNP_ID_265516058 A-to-I Human chr6 + 5658073 5658073 5658073 GAGGTGGGGAATTCAAGACCAGTCTGATGAACATGGAGGAACCCCTTCTCTACTAAAAGTACAAA GAGGTGGGGAATTCAAGACCAGTCTGATGAACGTGGAGGAACCCCTTCTCTACTAAAAGTACAAA A G FARS2 Ensembl:ENSG00000145982 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053580940 Functional Loss SNV dbSNP153 33..33 33 - - - 4943 RMVar_ID_4943 Human_SNP_ID_265535388 A-to-I Human chr6 + 5737275 5737275 5737275 AAGATCCTGGCCGGGCGCAATGGCTCACGCCTATAATCCCAGAGCTTCGGGAGGCCAAGGTGGGT AAGATCCTGGCCGGGCGCAATGGCTCACGCCTGTAATCCCAGAGCTTCGGGAGGCCAAGGTGGGT A G FARS2 Ensembl:ENSG00000145982 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs911717650 Functional Loss SNV dbSNP153 33..33 33 - - - 4944 RMVar_ID_4944 Human_SNP_ID_265590806 A-to-I Human chr6 + 5973522 5973522 5973522 GCATCATGCTGTCTGGAGAAACAGCCAAAGGGAACTATCCTCTGGAGGCTGTGCACATGCAGCAC GCATCATGCTGTCTGGAGAAACAGCCAAAGGGCACTATCCTCTGGAGGCTGTGCACATGCAGCAC A C PKMP5 Ensembl:ENSG00000215057 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1281518173 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1818857,Human_miRNA_ID_1838844,Human_miRNA_ID_1839988,Human_miRNA_ID_1864326,Human_miRNA_ID_1889879,Human_miRNA_ID_1892060,Human_miRNA_ID_1899895 4945 RMVar_ID_4945 Human_SNP_ID_265590807 A-to-I Human chr6 + 5973522 5973522 5973522 GCATCATGCTGTCTGGAGAAACAGCCAAAGGGAACTATCCTCTGGAGGCTGTGCACATGCAGCAC GCATCATGCTGTCTGGAGAAACAGCCAAAGGGGACTATCCTCTGGAGGCTGTGCACATGCAGCAC A G PKMP5 Ensembl:ENSG00000215057 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1281518173 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1818857,Human_miRNA_ID_1838844,Human_miRNA_ID_1839988,Human_miRNA_ID_1864326,Human_miRNA_ID_1889879,Human_miRNA_ID_1892060,Human_miRNA_ID_1899895 4946 RMVar_ID_4946 Human_SNP_ID_265590812 A-to-I Human chr6 + 5973544 5973544 5973544 AGCCAAAGGGAACTATCCTCTGGAGGCTGTGCACATGCAGCACCTGATTGCCTGTGAGGCAGAGG AGCCAAAGGGAACTATCCTCTGGAGGCTGTGCGCATGCAGCACCTGATTGCCTGTGAGGCAGAGG A G PKMP5 Ensembl:ENSG00000215057 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879192008 Functional Loss SNV dbSNP153 33..33 33 - - - 4947 RMVar_ID_4947 Human_SNP_ID_265590818 A-to-I Human chr6 + 5973579 5973579 5973579 TGCAGCACCTGATTGCCTGTGAGGCAGAGGCCACCATCTACCACTTGCAATTATTTGAGGAGTTC TGCAGCACCTGATTGCCTGTGAGGCAGAGGCCGCCATCTACCACTTGCAATTATTTGAGGAGTTC A G PKMP5 Ensembl:ENSG00000215057 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879070348 Functional Loss SNV dbSNP153 33..33 33 - - - 4948 RMVar_ID_4948 Human_SNP_ID_265762069 A-to-I Human chr6 - 6622667 6622667 6622667 ATGCATCATTGTCTATGATATCTGCAATGGAAATGATCACTAGGCAATTTCAGCCTTGCAAATCT ATGCATCATTGTCTATGATATCTGCAATGGAATTGATCACTAGGCAATTTCAGCCTTGCAAATCT T A LY86-AS1 Ensembl:ENSG00000216863 lincRNA exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1427395068 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_735365,Human_Splice_Rec_735379,Human_Splice_Rec_735393,Human_Splice_Rec_735405,Human_Splice_Rec_735417,Human_Splice_Rec_735427,Human_Splice_Rec_735447,Human_Splice_Rec_735449,Human_Splice_Rec_735451,Human_Splice_Rec_735453 4949 RMVar_ID_4949 Human_SNP_ID_265834845 A-to-I Human chr6 + 6895127 6895127 6895127 CTACTCGGGAGGTTGAGGCTGGAGGATTGCTTAAACCCGTGAGGCGGAAGTTGCAGTGAACTGAA CTACTCGGGAGGTTGAGGCTGGAGGATTGCTTCAACCCGTGAGGCGGAAGTTGCAGTGAACTGAA A C lnc-RREB1-9,lnc-RREB1-9:2,lnc-RREB1-9:3,lnc-RREB1-9:4,lnc-RREB1-9:5,lnc-RREB1-9:6 RNACentral:URS0000D574A6,RNACentral:URS00008B38DF,RNACentral:URS0000D597B9,RNACentral:URS00008B4FA1,RNACentral:URS0000D5DE54,RNACentral:URS0000D5B54A lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs944354601 Functional Loss SNV dbSNP153 33..33 33 - - - 4950 RMVar_ID_4950 Human_SNP_ID_265835705 A-to-I Human chr6 + 6898580 6898580 6898580 TGGAGTGCAATGACACCATCTTGGCTCACCACAACCTCCACCTCCGGTTTCAAGTGATTCTCCTG TGGAGTGCAATGACACCATCTTGGCTCACCACCACCTCCACCTCCGGTTTCAAGTGATTCTCCTG A C lnc-RREB1-9,lnc-RREB1-9:2,lnc-RREB1-9:3,lnc-RREB1-9:4,lnc-RREB1-9:5 RNACentral:URS0000D574A6,RNACentral:URS00008B38DF,RNACentral:URS00008B4FA1,RNACentral:URS0000D5DE54,RNACentral:URS0000D5B54A lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs6597234 Functional Loss SNV dbSNP153 33..33 33 - - - 4951 RMVar_ID_4951 Human_SNP_ID_265835706 A-to-I Human chr6 + 6898580 6898580 6898580 TGGAGTGCAATGACACCATCTTGGCTCACCACAACCTCCACCTCCGGTTTCAAGTGATTCTCCTG TGGAGTGCAATGACACCATCTTGGCTCACCACTACCTCCACCTCCGGTTTCAAGTGATTCTCCTG A T lnc-RREB1-9,lnc-RREB1-9:2,lnc-RREB1-9:3,lnc-RREB1-9:4,lnc-RREB1-9:5 RNACentral:URS0000D574A6,RNACentral:URS00008B38DF,RNACentral:URS00008B4FA1,RNACentral:URS0000D5DE54,RNACentral:URS0000D5B54A lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs6597234 Functional Loss SNV dbSNP153 33..33 33 - - - 4952 RMVar_ID_4952 Human_SNP_ID_265910125 A-to-I Human chr6 + 7176959 7176959 7176959 TGTAACTAGGCCAGACATGGTGGCTCACACCTATAATTCCAGCACTTTAGGAGGCTGAGGCGGAC TGTAACTAGGCCAGACATGGTGGCTCACACCTGTAATTCCAGCACTTTAGGAGGCTGAGGCGGAC A G RREB1 Ensembl:ENSG00000124782 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs770580480 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73104,RMVar_hsa_circ_125201,RMVar_hsa_circ_237028,RMVar_hsa_circ_328645,RMVar_hsa_circ_237029,RMVar_hsa_circ_237033,RMVar_hsa_circ_76302,RMVar_hsa_circ_278576,RMVar_hsa_circ_314845,RMVar_hsa_circ_322038,RMVar_hsa_circ_299331,RMVar_hsa_circ_120614,RMVar_hsa_circ_126517,RMVar_hsa_circ_89958,RMVar_hsa_circ_237035,RMVar_hsa_circ_237036,RMVar_hsa_circ_237034,RMVar_hsa_circ_237031,RMVar_hsa_circ_237032,RMVar_hsa_circ_237030 4953 RMVar_ID_4953 Human_SNP_ID_265923518 A-to-I Human chr6 + 7228691 7228691 7228691 CACATCTGGCTAATTTTCTTATTTTTTTTTATAGAGACAAGGTCTTGCTATGTTGCCCAGGCTAG CACATCTGGCTAATTTTCTTATTTTTTTTTATGGAGACAAGGTCTTGCTATGTTGCCCAGGCTAG A G RREB1 Ensembl:ENSG00000124782 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1047938267 Functional Loss SNV dbSNP153 33..33 33 - - - 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 4954 RMVar_ID_4954 Human_SNP_ID_265935759 A-to-I Human chr6 - 7268720 7268720 7268720 GGGCCCTTGGGTCAGCTGTCCCCACCCACTACACTGATGGTGAATGAGGCCAGAAGACAGGGGGC GGGCCCTTGGGTCAGCTGTCCCCACCCACTACTCTGATGGTGAATGAGGCCAGAAGACAGGGGGC T A SSR1 Ensembl:ENSG00000124783 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1165672972 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_667543 4955 RMVar_ID_4955 Human_SNP_ID_265939914 A-to-I Human chr6 - 7281518 7281518 7281518 TGTGGTTTAAAATATTTCTGTTCATATTTTCTAATTTGTTGCCGGAGGTCTTGGGTTTTCTATTT TGTGGTTTAAAATATTTCTGTTCATATTTTCTGATTTGTTGCCGGAGGTCTTGGGTTTTCTATTT T C SSR1 Ensembl:ENSG00000124783 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs537831335 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7624882,Human_RBP_ID_21364369,Human_RBP_ID_27757963 4956 RMVar_ID_4956 Human_SNP_ID_265940309 A-to-I Human chr6 - 7283218 7283218 7283218 ACAATTAGCCGAGCGAGGTGGTGCACGCCTGTAATCCCAGCTACTCATGAGGCTGAGGCAGGAGA ACAATTAGCCGAGCGAGGTGGTGCACGCCTGTGATCCCAGCTACTCATGAGGCTGAGGCAGGAGA T C SSR1 Ensembl:ENSG00000124783 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs995008532 Functional Loss SNV dbSNP153 33..33 33 - - - 4957 RMVar_ID_4957 Human_SNP_ID_265940839 A-to-I Human chr6 - 7285557 7285557 7285557 CTCCTGCTTCAGCTTTCCAAGTATTTGGGACCACAGGCGCACACCACAGGCCTGGCTAATGTTTT CTCCTGCTTCAGCTTTCCAAGTATTTGGGACCGCAGGCGCACACCACAGGCCTGGCTAATGTTTT T C SSR1 Ensembl:ENSG00000124783 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350772564 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7624922,Human_RBP_ID_15872168 4958 RMVar_ID_4958 Human_SNP_ID_265940845 A-to-I Human chr6 - 7285567 7285567 7285567 TCAAGCGATTCTCCTGCTTCAGCTTTCCAAGTATTTGGGACCACAGGCGCACACCACAGGCCTGG TCAAGCGATTCTCCTGCTTCAGCTTTCCAAGTGTTTGGGACCACAGGCGCACACCACAGGCCTGG T C SSR1 Ensembl:ENSG00000124783 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1329495568 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7624922,Human_RBP_ID_15872169,Human_RBP_ID_26018851 4959 RMVar_ID_4959 Human_SNP_ID_265941473 A-to-I Human chr6 - 7288391 7288390 7288391 GTTATTGTATAATTGTTAATCACTTTGCAAATAGGGGCTATCAAATTACCTATATTGGCATTGCT GTTATTGTATAATTGTTAATCACTTTGCAAAT_GGGGCTATCAAATTACCTATATTGGCATTGCT CT C SSR1 Ensembl:ENSG00000124783 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1262385462 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_667644,Human_RBP_ID_1048456,Human_RBP_ID_2025341,Human_RBP_ID_7625001,Human_RBP_ID_8216339,Human_RBP_ID_15872301,Human_RBP_ID_17307873,Human_RBP_ID_17420756,Human_RBP_ID_17536876,Human_RBP_ID_18373116,Human_RBP_ID_21902682,Human_RBP_ID_27758013 Human_miRNA_ID_154499 RMVar_hsa_circ_237046 4960 RMVar_ID_4960 Human_SNP_ID_265941474 A-to-I Human chr6 - 7288391 7288391 7288391 GTTATTGTATAATTGTTAATCACTTTGCAAATAGGGGCTATCAAATTACCTATATTGGCATTGCT GTTATTGTATAATTGTTAATCACTTTGCAAATTGGGGCTATCAAATTACCTATATTGGCATTGCT T A SSR1 Ensembl:ENSG00000124783 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs766026861 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_667644,Human_RBP_ID_1048456,Human_RBP_ID_2025341,Human_RBP_ID_7625001,Human_RBP_ID_8216339,Human_RBP_ID_15872301,Human_RBP_ID_17307873,Human_RBP_ID_17420756,Human_RBP_ID_17536876,Human_RBP_ID_18373116,Human_RBP_ID_21902682,Human_RBP_ID_27758013 Human_miRNA_ID_154499 RMVar_hsa_circ_237046 4961 RMVar_ID_4961 Human_SNP_ID_265944438 A-to-I Human chr6 - 7300932 7300932 7300932 TTATTCAGATGTTAAGATCTGTTGCTGGGTACAGTGGCTCACACCTGTAATCTCAGCACTTTGGG TTATTCAGATGTTAAGATCTGTTGCTGGGTACGGTGGCTCACACCTGTAATCTCAGCACTTTGGG T C SSR1 Ensembl:ENSG00000124783 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1214665127 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16587,RMVar_hsa_circ_287835,RMVar_hsa_circ_41850,RMVar_hsa_circ_237046,RMVar_hsa_circ_348087,RMVar_hsa_circ_237048,RMVar_hsa_circ_237049,RMVar_hsa_circ_364691,RMVar_hsa_circ_114827,RMVar_hsa_circ_363692,RMVar_hsa_circ_237051 4962 RMVar_ID_4962 Human_SNP_ID_265955767 A-to-I Human chr6 - 7339031 7339031 7339031 ACACTGCTGTGCGCCATGTGTTGCTCAGACAGAGTGTGCTGGGCATCAAGGTGAAGATCATGCTG ACACTGCTGTGCGCCATGTGTTGCTCAGACAGGGTGTGCTGGGCATCAAGGTGAAGATCATGCTG T C AL139095.2,SSR1,CAGE1 Ensembl:ENSG00000220472,Ensembl:ENSG00000124783,Ensembl:ENSG00000164304 Pseudogene,Protein coding,Protein coding exon,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878865712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_170878,Human_RBP_ID_4915462,Human_RBP_ID_18086404 4963 RMVar_ID_4963 Human_SNP_ID_265970739 A-to-I Human chr6 + 7395917 7395908 7395918 TTCTGTAGAGACGGGGTTTCTCCATGTTGACCAGGCTGGTTTTGAACTCCTGAGCTCAAGTGATC TTCTGTAGAGACGGGGTTTCTCCA__________GCTGGTTTTGAACTCCTGAGCTCAAGTGATC ATGTTGACCAG A RIOK1 Ensembl:ENSG00000124784 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900186758 Functional Loss DEL dbSNP153 25..34 33 - - - RMVar_hsa_circ_7793,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,RMVar_hsa_circ_308509,RMVar_hsa_circ_338792,RMVar_hsa_circ_35638 4964 RMVar_ID_4964 Human_SNP_ID_266005284 A-to-I Human chr6 - 7516965 7516965 7516965 AAGGGTATGGCTCTCTTGGCATGATGACCAGCATGCTAGTGTGTCCACATGGCAAGACAGTAGAA AAGGGTATGGCTCTCTTGGCATGATGACCAGCGTGCTAGTGTGTCCACATGGCAAGACAGTAGAA T C AL138878.2 Ensembl:ENSG00000234115 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs952172189 Functional Loss SNV dbSNP153 33..33 33 - - - 4965 RMVar_ID_4965 Human_SNP_ID_266026796 A-to-I Human chr6 + 7598004 7598004 7598004 TCTTCTGCCTCAGGTCCCGAGTAGCTGGGACTACAGGCACCTGCCACCACGCCTGGCTAATTTTC TCTTCTGCCTCAGGTCCCGAGTAGCTGGGACTGCAGGCACCTGCCACCACGCCTGGCTAATTTTC A G SNRNP48 Ensembl:ENSG00000168566 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1172451340 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60208,RMVar_hsa_circ_19055 4966 RMVar_ID_4966 Human_SNP_ID_266026811 A-to-I Human chr6 + 7598049 7598049 7598049 ACCACGCCTGGCTAATTTTCTTGTATTTTTTTAGTAGAGACGGGGTTTCACTGTGTTAGCCACGA ACCACGCCTGGCTAATTTTCTTGTATTTTTTTGGTAGAGACGGGGTTTCACTGTGTTAGCCACGA A G SNRNP48 Ensembl:ENSG00000168566 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs902740572 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60208,RMVar_hsa_circ_19055 4967 RMVar_ID_4967 Human_SNP_ID_266029998 A-to-I Human chr6 + 7611383 7611383 7611383 TATGTATTTTTAAATTTTTTTGTAGAGACAGGATCTCACTATGTTCTCCAGCTGGTCTCAAGCTC TATGTATTTTTAAATTTTTTTGTAGAGACAGGGTCTCACTATGTTCTCCAGCTGGTCTCAAGCTC A G SNRNP48 Ensembl:ENSG00000168566 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924315971 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_668327,Human_RBP_ID_3814831,Human_RBP_ID_15942058,Human_RBP_ID_18373583 RMVar_hsa_circ_109071,RMVar_hsa_circ_237074 4968 RMVar_ID_4968 Human_SNP_ID_266096366 A-to-I Human chr6 + 7881542 7881542 7881542 ACCAGACTTTTAAAAAAAAAGAGTTTATTTAGAAAGTATCATAGTGTAAACAAACAAATTGTACC ACCAGACTTTTAAAAAAAAAGAGTTTATTTAGGAAGTATCATAGTGTAAACAAACAAATTGTACC A G BMP6 Ensembl:ENSG00000153162 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1347407495 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3018837,Human_RBP_ID_24172159 4969 RMVar_ID_4969 Human_SNP_ID_266099387 A-to-I Human chr6 - 7891108 7891108 7891108 TGACAACTTCTGTGTAACTGGATTTTCTGGAAATATCCAGTGTAGCTCCAGGGACATCACTTTTA TGACAACTTCTGTGTAACTGGATTTTCTGGAAGTATCCAGTGTAGCTCCAGGGACATCACTTTTA T C BLOC1S5-TXNDC5,TXNDC5 Ensembl:ENSG00000259040,Ensembl:ENSG00000239264 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs554421515 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64775,RMVar_hsa_circ_63059,RMVar_hsa_circ_237086,RMVar_hsa_circ_370266 4970 RMVar_ID_4970 Human_SNP_ID_266116574 A-to-I Human chr6 - 7959119 7959119 7959119 ATTTAAAAAGCAGAGGCCGAGCACGGTGGCTTATGCCTGTAATCCTAGCACTTTGGGAGGCTGAG ATTTAAAAAGCAGAGGCCGAGCACGGTGGCTTGTGCCTGTAATCCTAGCACTTTGGGAGGCTGAG T C BLOC1S5-TXNDC5 Ensembl:ENSG00000259040 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs759855395 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80608,RMVar_hsa_circ_237089 4971 RMVar_ID_4971 Human_SNP_ID_266128101 A-to-I Human chr6 - 8008584 8008584 8008584 AGTTTCGCTCTTGTTGCCCAGGCTGGAGTGCAATGGCGCAACCTTGGCTCACTGCAACCTGCGCC AGTTTCGCTCTTGTTGCCCAGGCTGGAGTGCAGTGGCGCAACCTTGGCTCACTGCAACCTGCGCC T C BLOC1S5-TXNDC5 Ensembl:ENSG00000259040 Protein coding intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1216694070 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80608,RMVar_hsa_circ_237089 4972 RMVar_ID_4972 Human_SNP_ID_266129124 A-to-I Human chr6 - 8012952 8012952 8012952 CTTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGTGCCTAGCCAGTTTGTAACATT CTTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGTGCCTAGCCAGTTTGTAACATT T C BLOC1S5-TXNDC5 Ensembl:ENSG00000259040 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs935720061 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80608,RMVar_hsa_circ_237089 4973 RMVar_ID_4973 Human_SNP_ID_266129125 A-to-I Human chr6 - 8012958 8012958 8012958 TGCCCACTTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGTGCCTAGCCAGTTTGT TGCCCACTTCAGCCTCCCAAAGTGCTGGGATTGCAGGCATGAGCCACTGTGCCTAGCCAGTTTGT T C BLOC1S5-TXNDC5 Ensembl:ENSG00000259040 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs891114541 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80608,RMVar_hsa_circ_237089 4974 RMVar_ID_4974 Human_SNP_ID_266133534 A-to-I Human chr6 - 8030789 8030789 8030789 TGGCTCACTGCAACCTCTGTCTTCTGGGTTCAAGCCATTCTCCTGCCTCAGCCTCCGGACTAGCT TGGCTCACTGCAACCTCTGTCTTCTGGGTTCAGGCCATTCTCCTGCCTCAGCCTCCGGACTAGCT T C BLOC1S5-TXNDC5,EEF1E1-BLOC1S5,BLOC1S5 Ensembl:ENSG00000259040,Ensembl:ENSG00000265818,Ensembl:ENSG00000188428 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1413241785 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33966,RMVar_hsa_circ_265508,RMVar_hsa_circ_315135,RMVar_hsa_circ_88114,RMVar_hsa_circ_237091 4975 RMVar_ID_4975 Human_SNP_ID_266148936 A-to-I Human chr6 - 8094002 8094002 8094002 TTGAGGTTAGGAGTCCGAGATCAGCCTGGCCAACATGGTGGAACCCCCATCTCTGCTAAAAACAG TTGAGGTTAGGAGTCCGAGATCAGCCTGGCCATCATGGTGGAACCCCCATCTCTGCTAAAAACAG T A EEF1E1,EEF1E1-BLOC1S5 Ensembl:ENSG00000124802,Ensembl:ENSG00000265818 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1035977241 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33124 4976 RMVar_ID_4976 Human_SNP_ID_266228098 A-to-I Human chr6 - 8413146 8413146 8413146 TTTGATGGTGTTATTTAAATTGATTCTCTGTTATAAGAGTAAACTGATGAGTTGAAGTCTGGAGA TTTGATGGTGTTATTTAAATTGATTCTCTGTTGTAAGAGTAAACTGATGAGTTGAAGTCTGGAGA T C SLC35B3 Ensembl:ENSG00000124786 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1381304226 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_669306,Human_RBP_ID_1676845,Human_RBP_ID_18374213 4977 RMVar_ID_4977 Human_SNP_ID_266228122 A-to-I Human chr6 - 8413317 8413317 8413317 CCACGTCTAGCAGACTTTACAATAAAATGTCAATATGAAGGACTGTAATTCCTAGCAGTTTATTG CCACGTCTAGCAGACTTTACAATAAAATGTCAGTATGAAGGACTGTAATTCCTAGCAGTTTATTG T C SLC35B3 Ensembl:ENSG00000124786 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs909617402 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_669310,Human_RBP_ID_22514714 4978 RMVar_ID_4978 Human_SNP_ID_266527605 A-to-I Human chr6 - 9618951 9618951 9618951 GAGATCGAGACCATCCTGGCTGGCGCGGTGAAACTCCGTCTCTACTAAAAATACAAAAAATTAGC GAGATCGAGACCATCCTGGCTGGCGCGGTGAACCTCCGTCTCTACTAAAAATACAAAAAATTAGC T G OFCC1 Ensembl:ENSG00000181355 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054213958 Functional Loss SNV dbSNP153 33..33 33 - - - 4979 RMVar_ID_4979 Human_SNP_ID_266771306 A-to-I Human chr6 + 10532703 10532703 10532703 GTTGCCAGTGCTGGTCTTGAACTCCTGGGCCCAAGCGATCCTCCTGCCTCAGCCTCGTGAGCCAC GTTGCCAGTGCTGGTCTTGAACTCCTGGGCCCGAGCGATCCTCCTGCCTCAGCCTCGTGAGCCAC A G GCNT2 Ensembl:ENSG00000111846 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1434300094 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15581779 4980 RMVar_ID_4980 Human_SNP_ID_266771964 A-to-I Human chr6 + 10534758 10534758 10534758 GGTGGCATGCACTGTAGTCTCAGCTGCTGGAGAAGTTGAGGCAGGAGGATCACTTGAGCCCAGGA GGTGGCATGCACTGTAGTCTCAGCTGCTGGAGGAGTTGAGGCAGGAGGATCACTTGAGCCCAGGA A G GCNT2 Ensembl:ENSG00000111846 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1480629153 Functional Loss SNV dbSNP153 33..33 33 - - - 4981 RMVar_ID_4981 Human_SNP_ID_266771979 A-to-I Human chr6 + 10534825 10534825 10534825 TCAAGGGCACAGTGAGCTGCAATAGCACCACTACCCTCAGACTGGGCAACAGAGTGAGACTCTGT TCAAGGGCACAGTGAGCTGCAATAGCACCACTGCCCTCAGACTGGGCAACAGAGTGAGACTCTGT A G GCNT2 Ensembl:ENSG00000111846 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs916833056 Functional Loss SNV dbSNP153 33..33 33 - - - 4982 RMVar_ID_4982 Human_SNP_ID_266772468 A-to-I Human chr6 + 10536425 10536425 10536425 TTGCCCAGGCTGGAGTGCAGTGGCGTGATCTCAGCTCACTGCAAGTTCTCCTCCCGGGTTCACGC TTGCCCAGGCTGGAGTGCAGTGGCGTGATCTCGGCTCACTGCAAGTTCTCCTCCCGGGTTCACGC A G GCNT2 Ensembl:ENSG00000111846 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1485535532 Functional Loss SNV dbSNP153 33..33 33 - - - 4983 RMVar_ID_4983 Human_SNP_ID_266773766 A-to-I Human chr6 + 10539887 10539887 10539887 AGGAGGATCAGAGGATTGCTTGAGACCAGCCTAGGCAACATAGTGAAATTCCATCTCTACAAAAA AGGAGGATCAGAGGATTGCTTGAGACCAGCCTGGGCAACATAGTGAAATTCCATCTCTACAAAAA A G GCNT2 Ensembl:ENSG00000111846 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1418499476 Functional Loss SNV dbSNP153 33..33 33 - - - 4984 RMVar_ID_4984 Human_SNP_ID_266773771 A-to-I Human chr6 + 10539896 10539896 10539896 AGAGGATTGCTTGAGACCAGCCTAGGCAACATAGTGAAATTCCATCTCTACAAAAAATACAAAAG AGAGGATTGCTTGAGACCAGCCTAGGCAACATCGTGAAATTCCATCTCTACAAAAAATACAAAAG A C GCNT2 Ensembl:ENSG00000111846 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444828987 Functional Loss SNV dbSNP153 33..33 33 - - - 4985 RMVar_ID_4985 Human_SNP_ID_266775124 A-to-I Human chr6 + 10544050 10544050 10544050 AAAATAAATAAATGGGCCAGGCCTGGTGGCTCACGCCTGTAATCCCAGAACTTTGGGAGGCCGAG AAAATAAATAAATGGGCCAGGCCTGGTGGCTCGCGCCTGTAATCCCAGAACTTTGGGAGGCCGAG A G GCNT2 Ensembl:ENSG00000111846 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1184898789 Functional Loss SNV dbSNP153 33..33 33 - - - 4986 RMVar_ID_4986 Human_SNP_ID_266777046 A-to-I Human chr6 + 10550620 10550620 10550620 TAAAGTGATCTCCCCACCTCAGCCACCCAAGTAGATGGCATGCACCACTGTGCCTGGCTAACTTT TAAAGTGATCTCCCCACCTCAGCCACCCAAGTGGATGGCATGCACCACTGTGCCTGGCTAACTTT A G GCNT2 Ensembl:ENSG00000111846 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1184695294 Functional Loss SNV dbSNP153 33..33 33 - - - 4987 RMVar_ID_4987 Human_SNP_ID_266777062 A-to-I Human chr6 + 10550683 10550683 10550683 TTTTAATTTTTTTGTAATGACAAGGTCTCACTATGTTGCTCAAGCTGGTCCCAAACTCCTGGGCT TTTTAATTTTTTTGTAATGACAAGGTCTCACTCTGTTGCTCAAGCTGGTCCCAAACTCCTGGGCT A C GCNT2 Ensembl:ENSG00000111846 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs773439704 Functional Loss SNV dbSNP153 33..33 33 - - - 4988 RMVar_ID_4988 Human_SNP_ID_266777063 A-to-I Human chr6 + 10550683 10550683 10550683 TTTTAATTTTTTTGTAATGACAAGGTCTCACTATGTTGCTCAAGCTGGTCCCAAACTCCTGGGCT TTTTAATTTTTTTGTAATGACAAGGTCTCACTGTGTTGCTCAAGCTGGTCCCAAACTCCTGGGCT A G GCNT2 Ensembl:ENSG00000111846 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs773439704 Functional Loss SNV dbSNP153 33..33 33 - - - 4989 RMVar_ID_4989 Human_SNP_ID_266785425 A-to-I Human chr6 + 10578244 10578244 10578244 GAAACCCCGTGTCTAATAAAAACACAAAAATTAGCTGGACACATCTATAATCCCAGCTACTCTGG GAAACCCCGTGTCTAATAAAAACACAAAAATTGGCTGGACACATCTATAATCCCAGCTACTCTGG A G GCNT2 Ensembl:ENSG00000111846 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1426712530 Functional Loss SNV dbSNP153 33..33 33 - - - 4990 RMVar_ID_4990 Human_SNP_ID_266796029 A-to-I Human chr6 + 10614478 10614478 10614478 AAACCCTATCTCTACTAAAAATACAAAAAATTAGCTGGACGTTAGTGGCACGCCCCTCTAGTCCC AAACCCTATCTCTACTAAAAATACAAAAAATTTGCTGGACGTTAGTGGCACGCCCCTCTAGTCCC A T GCNT2 Ensembl:ENSG00000111846 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1446110770 Functional Loss SNV dbSNP153 33..33 33 - - - 4991 RMVar_ID_4991 Human_SNP_ID_266797672 A-to-I Human chr6 + 10619543 10619543 10619543 GCCTAATTTTTAAAAAAATTTTTAGTAGAGATAGGGTCTCACTATGTTGCCCAGGCTGGTCTCGG GCCTAATTTTTAAAAAAATTTTTAGTAGAGATCGGGTCTCACTATGTTGCCCAGGCTGGTCTCGG A C GCNT2 Ensembl:ENSG00000111846 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1315514972 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_738113 4992 RMVar_ID_4992 Human_SNP_ID_266799967 A-to-I Human chr6 + 10628875 10628875 10628875 AAACCCCATCTCTACTAAAAAATATAAAAATTAGCCGGGCTTTGTGGCATGTGCCTGTAATCCCA AAACCCCATCTCTACTAAAAAATATAAAAATTGGCCGGGCTTTGTGGCATGTGCCTGTAATCCCA A G GCNT2 Ensembl:ENSG00000111846 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1398392067 Functional Loss SNV dbSNP153 33..33 33 - - - 4993 RMVar_ID_4993 Human_SNP_ID_266816420 A-to-I Human chr6 - 10693821 10693821 10693821 GGAAGGCTGAGGTGGGAGGATTGCTTGAGCCCAGGAGGTCGAGGCTGCAGTGAGCCGAGATCGCT GGAAGGCTGAGGTGGGAGGATTGCTTGAGCCCTGGAGGTCGAGGCTGCAGTGAGCCGAGATCGCT T A C6orf52 Ensembl:ENSG00000137434 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1178079461 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115917,RMVar_hsa_circ_237098 4994 RMVar_ID_4994 Human_SNP_ID_266819424 A-to-I Human chr6 + 10704770 10704770 10704770 CTCTCCTAGGAGTCTGTCCTTGCAGTGGCTGGAGATGAAGAAGTTATAAGGTTTTTTGACTGTGA CTCTCCTAGGAGTCTGTCCTTGCAGTGGCTGGGGATGAAGAAGTTATAAGGTTTTTTGACTGTGA A G PAK1IP1 Ensembl:ENSG00000111845 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs752400013 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_948037,Human_RBP_ID_2003679,Human_RBP_ID_5121838,Human_RBP_ID_5397898,Human_RBP_ID_15584949,Human_RBP_ID_19130122,Human_RBP_ID_24126512,Human_RBP_ID_26771861 Human_Splice_Rec_738196,Human_Splice_Rec_738197 Human_miRNA_ID_2972928,Human_miRNA_ID_3006113 RMVar_hsa_circ_91689,RMVar_hsa_circ_237104,RMVar_hsa_circ_237101,RMVar_hsa_circ_291716,RMVar_hsa_circ_110872,RMVar_hsa_circ_237105,RMVar_hsa_circ_237107,RMVar_hsa_circ_126681,RMVar_hsa_circ_284854,RMVar_hsa_circ_303939,RMVar_hsa_circ_237106,RMVar_hsa_circ_237108 4995 RMVar_ID_4995 Human_SNP_ID_266826932 A-to-I Human chr6 + 10727714 10727714 10727714 GTGGTGGCGGACGCCTGTAGTCCGAGTTACTCAGGAGGCTGAGACTTGAGAATTGCTTGATCCCA GTGGTGGCGGACGCCTGTAGTCCGAGTTACTCGGGAGGCTGAGACTTGAGAATTGCTTGATCCCA A G TMEM14C Ensembl:ENSG00000111843 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs773785454 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122395,RMVar_hsa_circ_237110,RMVar_hsa_circ_328027,RMVar_hsa_circ_237111 4996 RMVar_ID_4996 Human_SNP_ID_266826938 A-to-I Human chr6 + 10727741 10727741 10727741 TACTCAGGAGGCTGAGACTTGAGAATTGCTTGATCCCAGGAGGTGGAGGTTGCAGTGAGCCAAGA TACTCAGGAGGCTGAGACTTGAGAATTGCTTGGTCCCAGGAGGTGGAGGTTGCAGTGAGCCAAGA A G TMEM14C Ensembl:ENSG00000111843 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs563077960 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122395,RMVar_hsa_circ_237110,RMVar_hsa_circ_328027,RMVar_hsa_circ_237111 4997 RMVar_ID_4997 Human_SNP_ID_266827417 A-to-I Human chr6 + 10729548 10729548 10729548 CCTGTAATCCCAGCAATTTGGGAGGCAGAGGCAGGCGGATCACCTGATGTCAGGGGTTCAAGACC CCTGTAATCCCAGCAATTTGGGAGGCAGAGGCGGGCGGATCACCTGATGTCAGGGGTTCAAGACC A G TMEM14C Ensembl:ENSG00000111843 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1176086008 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17576215 RMVar_hsa_circ_115893,RMVar_hsa_circ_237112,RMVar_hsa_circ_237113 4998 RMVar_ID_4998 Human_SNP_ID_266827429 A-to-I Human chr6 + 10729593 10729593 10729593 GATGTCAGGGGTTCAAGACCATCCTGGCCAACATTGCGAAACCCCGTCTCTATGAAAAATACAAA GATGTCAGGGGTTCAAGACCATCCTGGCCAACGTTGCGAAACCCCGTCTCTATGAAAAATACAAA A G TMEM14C Ensembl:ENSG00000111843 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1272381516 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115893,RMVar_hsa_circ_237112,RMVar_hsa_circ_237113 4999 RMVar_ID_4999 Human_SNP_ID_266827466 A-to-I Human chr6 + 10729717 10729717 10729717 GGAGAATTGCTTCAACCTGGGAAGCGGAGATTACAGTGAGCTGAGATCATGCCACTGCACTCCAG GGAGAATTGCTTCAACCTGGGAAGCGGAGATTGCAGTGAGCTGAGATCATGCCACTGCACTCCAG A G TMEM14C Ensembl:ENSG00000111843 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1013005367 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115893,RMVar_hsa_circ_237112,RMVar_hsa_circ_237113 5000 RMVar_ID_5000 Human_SNP_ID_266827518 A-to-I Human chr6 + 10729896 10729896 10729896 AGAGCGGGCGGATCACTTGAGGTCAGGAGTTCAAGACCAGTCTGCCCAACATGGTGAAACCCCAT AGAGCGGGCGGATCACTTGAGGTCAGGAGTTCGAGACCAGTCTGCCCAACATGGTGAAACCCCAT A G TMEM14C Ensembl:ENSG00000111843 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs931759892 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115893,RMVar_hsa_circ_237112,RMVar_hsa_circ_237113 5001 RMVar_ID_5001 Human_SNP_ID_266828090 A-to-I Human chr6 + 10731873 10731873 10731873 CGACTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCATGCCCGGCAGCCACTG CGACTGCCTCAGCCTCCCAAAGTGCTGGGATTGCAGGTGTGAGCCACCATGCCCGGCAGCCACTG A G RF00017-1033 RNACentral:URS0000984FD7 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1013735239 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115893,RMVar_hsa_circ_237113 5002 RMVar_ID_5002 Human_SNP_ID_266830690 A-to-I Human chr6 + 10741635 10741635 10741635 GTGGGGACTTGGAGAACTTTTCTGTCTAGCTAAAGGATTATAAACACACTAATCAGCACTCTGTG GTGGGGACTTGGAGAACTTTTCTGTCTAGCTAGAGGATTATAAACACACTAATCAGCACTCTGTG A G RF00017-1033 RNACentral:URS0000984FD7 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256427623 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115893,RMVar_hsa_circ_237113 5003 RMVar_ID_5003 Human_SNP_ID_266832414 A-to-I Human chr6 + 10748358 10748354 10748358 GCCTCTGCCTCCTGGGCTCAAGCCATCCTCCCACCTCAGCCTCCCAAGTAGCTGGGATTACAGGT GCCTCTGCCTCCTGGGCTCAAGCCATCCT____CCTCAGCCTCCCAAGTAGCTGGGATTACAGGT TCCCA T TMEM14B,AL024498.2 Ensembl:ENSG00000137210,Ensembl:ENSG00000272162 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1318874342 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_115893,RMVar_hsa_circ_85784,RMVar_hsa_circ_237113,RMVar_hsa_circ_237114 5004 RMVar_ID_5004 Human_SNP_ID_266833640 A-to-I Human chr6 + 10752582 10752582 10752582 GGATTCAAGTGGTTCTCCTGCCTCAGCCTTCTAGGTAGTTGGGATTACAGGTGTCTCCCACCATG GGATTCAAGTGGTTCTCCTGCCTCAGCCTTCTGGGTAGTTGGGATTACAGGTGTCTCCCACCATG A G TMEM14B,AL024498.2 Ensembl:ENSG00000137210,Ensembl:ENSG00000272162 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs972526805 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17576216 RMVar_hsa_circ_237115,RMVar_hsa_circ_85784,RMVar_hsa_circ_237114,RMVar_hsa_circ_285635,RMVar_hsa_circ_237116,RMVar_hsa_circ_373050 5005 RMVar_ID_5005 Human_SNP_ID_266833748 A-to-I Human chr6 + 10753007 10753007 10753007 CGTATAATCCCAGCACTTTGGGAGACCGAGGCAGGCGGCTCACCTGAGGTCGGGAGTTGGAGACC CGTATAATCCCAGCACTTTGGGAGACCGAGGCCGGCGGCTCACCTGAGGTCGGGAGTTGGAGACC A C TMEM14B,AL024498.2 Ensembl:ENSG00000137210,Ensembl:ENSG00000272162 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs746479880 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_237115,RMVar_hsa_circ_85784,RMVar_hsa_circ_237114,RMVar_hsa_circ_285635,RMVar_hsa_circ_237116,RMVar_hsa_circ_373050 5006 RMVar_ID_5006 Human_SNP_ID_266833749 A-to-I Human chr6 + 10753007 10753007 10753007 CGTATAATCCCAGCACTTTGGGAGACCGAGGCAGGCGGCTCACCTGAGGTCGGGAGTTGGAGACC CGTATAATCCCAGCACTTTGGGAGACCGAGGCGGGCGGCTCACCTGAGGTCGGGAGTTGGAGACC A G TMEM14B,AL024498.2 Ensembl:ENSG00000137210,Ensembl:ENSG00000272162 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs746479880 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_237115,RMVar_hsa_circ_85784,RMVar_hsa_circ_237114,RMVar_hsa_circ_285635,RMVar_hsa_circ_237116,RMVar_hsa_circ_373050 5007 RMVar_ID_5007 Human_SNP_ID_266833778 A-to-I Human chr6 + 10753125 10753125 10753125 GGGCTTGGTGGCTGTCACCTGTAATCCCAGCCACTCAGGAGGTTGAGGCAGGAGAATCGCTTGAA GGGCTTGGTGGCTGTCACCTGTAATCCCAGCCGCTCAGGAGGTTGAGGCAGGAGAATCGCTTGAA A G TMEM14B,AL024498.2 Ensembl:ENSG00000137210,Ensembl:ENSG00000272162 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054130409 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_237115,RMVar_hsa_circ_85784,RMVar_hsa_circ_237114,RMVar_hsa_circ_285635,RMVar_hsa_circ_237116,RMVar_hsa_circ_373050 5008 RMVar_ID_5008 Human_SNP_ID_266834843 A-to-I Human chr6 + 10757242 10757242 10757242 TAGGCTGGAGGGCAGTGGTACAATCATATCTCACTGTAGCCTCAAACTCTTGGGTTCAGTCATCC TAGGCTGGAGGGCAGTGGTACAATCATATCTCGCTGTAGCCTCAAACTCTTGGGTTCAGTCATCC A G TMEM14B,AL024498.2 Ensembl:ENSG00000137210,Ensembl:ENSG00000272162 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1055427447 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_334180 5009 RMVar_ID_5009 Human_SNP_ID_266836213 A-to-I Human chr6 + 10761845 10761845 10761845 TCAAGCGATTCTCCTGTCTCAGCCTCCCAAGTAGCTGGGATTACAGACATGCACCACCATGGCTC TCAAGCGATTCTCCTGTCTCAGCCTCCCAAGTCGCTGGGATTACAGACATGCACCACCATGGCTC A C TMEM14B,AL024498.2 Ensembl:ENSG00000137210,Ensembl:ENSG00000272162 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1020727888 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_334180 5010 RMVar_ID_5010 Human_SNP_ID_266836352 A-to-I Human chr6 + 10762426 10762426 10762426 TCACTGTACTGTAACCTCTGCCTCCCAGGTTCAAGCAATTCTCCTACCTCAGCCGCCCAAGTAGC TCACTGTACTGTAACCTCTGCCTCCCAGGTTCCAGCAATTCTCCTACCTCAGCCGCCCAAGTAGC A C TMEM14B,AL024498.2 Ensembl:ENSG00000137210,Ensembl:ENSG00000272162 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1488820360 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_334180 5011 RMVar_ID_5011 Human_SNP_ID_266842191 A-to-I Human chr6 + 10786202 10786202 10786202 GGGAGGCAGAGGTTGCAGTGAGCCAAGATCGCACCACTGCACTCAGCCTGGGCGACAAGAGCAAA GGGAGGCAGAGGTTGCAGTGAGCCAAGATCGCGCCACTGCACTCAGCCTGGGCGACAAGAGCAAA A G TMEM14B,AL024498.2 Ensembl:ENSG00000137210,Ensembl:ENSG00000272162 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs574431668 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8626750 5012 RMVar_ID_5012 Human_SNP_ID_266842657 A-to-I Human chr6 + 10788036 10788035 10788037 ACAACCTTGATCTTTTTTTGATTTTTTGAGACAGTGTCTCGCTCTGTTGCCCAGGCTGGGGTGCA ACAACCTTGATCTTTTTTTGATTTTTTGAGAC__TGTCTCGCTCTGTTGCCCAGGCTGGGGTGCA CAG C TMEM14B,AL024498.2 Ensembl:ENSG00000137210,Ensembl:ENSG00000272162 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215665813 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_15588317 5013 RMVar_ID_5013 Human_SNP_ID_266842658 A-to-I Human chr6 + 10788036 10788036 10788036 ACAACCTTGATCTTTTTTTGATTTTTTGAGACAGTGTCTCGCTCTGTTGCCCAGGCTGGGGTGCA ACAACCTTGATCTTTTTTTGATTTTTTGAGACTGTGTCTCGCTCTGTTGCCCAGGCTGGGGTGCA A T TMEM14B,AL024498.2 Ensembl:ENSG00000137210,Ensembl:ENSG00000272162 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879179334 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15588317 5014 RMVar_ID_5014 Human_SNP_ID_266842696 A-to-I Human chr6 - 10788180 10788180 10788180 TGAGACCAGCCTGGGCAATATGGCAAAACTCCATCTCTACAAAAAAATACAAAAATTAGCCAGAT TGAGACCAGCCTGGGCAATATGGCAAAACTCCGTCTCTACAAAAAAATACAAAAATTAGCCAGAT T C MAK Ensembl:ENSG00000111837 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1443986732 Functional Loss SNV dbSNP153 33..33 33 - - - 5015 RMVar_ID_5015 Human_SNP_ID_266842781 A-to-I Human chr6 - 10788560 10788560 10788560 CCTGGCTAATTTTTTGTATTTTTAATAGAGACAGTGTTTCACCATGTTGGCCAGGCTAGTCTTGA CCTGGCTAATTTTTTGTATTTTTAATAGAGACGGTGTTTCACCATGTTGGCCAGGCTAGTCTTGA T C MAK Ensembl:ENSG00000111837 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1467027020 Functional Loss SNV dbSNP153 33..33 33 - - - 5016 RMVar_ID_5016 Human_SNP_ID_266845151 A-to-I Human chr6 + 10798360 10798360 10798360 CGGTCTCAAGCTCCTGACCTCGTGATCCGCCCACCTTGGCCTCTCAAAGTGCTAGGATTACAGGT CGGTCTCAAGCTCCTGACCTCGTGATCCGCCCGCCTTGGCCTCTCAAAGTGCTAGGATTACAGGT A G TMEM14B,AL024498.2 Ensembl:ENSG00000137210,Ensembl:ENSG00000272162 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1461400273 Functional Loss SNV dbSNP153 33..33 33 - - - 5017 RMVar_ID_5017 Human_SNP_ID_266846646 A-to-I Human chr6 + 10804482 10804482 10804482 ATCCTGCCTCAGCCTCCCGAGCAGCGGGGATTACAGGGGCACACCACCATGCCCAGCTAATTTTT ATCCTGCCTCAGCCTCCCGAGCAGCGGGGATTGCAGGGGCACACCACCATGCCCAGCTAATTTTT A G TMEM14B,AL024498.2 Ensembl:ENSG00000137210,Ensembl:ENSG00000272162 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350345072 Functional Loss SNV dbSNP153 33..33 33 - - - 5018 RMVar_ID_5018 Human_SNP_ID_267144730 A-to-I Human chr6 + 12038381 12038381 12038381 AGAGGCATACAGGGTACACAGAAAAAGTTAAGAATCATCCTCTGGATGGGCGCGGTGGCTCACGA AGAGGCATACAGGGTACACAGAAAAAGTTAAGCATCATCCTCTGGATGGGCGCGGTGGCTCACGA A C HIVEP1 Ensembl:ENSG00000095951 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs972503017 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89332,RMVar_hsa_circ_237173,RMVar_hsa_circ_346820,RMVar_hsa_circ_338569 5019 RMVar_ID_5019 Human_SNP_ID_267144731 A-to-I Human chr6 + 12038381 12038381 12038381 AGAGGCATACAGGGTACACAGAAAAAGTTAAGAATCATCCTCTGGATGGGCGCGGTGGCTCACGA AGAGGCATACAGGGTACACAGAAAAAGTTAAGGATCATCCTCTGGATGGGCGCGGTGGCTCACGA A G HIVEP1 Ensembl:ENSG00000095951 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs972503017 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89332,RMVar_hsa_circ_237173,RMVar_hsa_circ_346820,RMVar_hsa_circ_338569 5020 RMVar_ID_5020 Human_SNP_ID_267334271 A-to-I Human chr6 + 12820205 12820205 12820205 TTTTGTTGTTGTTTTGTTTTGTTTTTTGAGATAGAGTCTCGCTCTGTTGCCAAGGCTGGAGTGCG TTTTGTTGTTGTTTTGTTTTGTTTTTTGAGATGGAGTCTCGCTCTGTTGCCAAGGCTGGAGTGCG A G PHACTR1 Ensembl:ENSG00000112137 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,temporal_cortex - 29129909,30559470 RNA-Seq:(High) rs577108482 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21632 5021 RMVar_ID_5021 Human_SNP_ID_267343037 A-to-I Human chr6 + 12857447 12857447 12857447 TCCTGGCCAACATGGCTGTCTTTACTAAAAATACAAAAATTAGCTGTGTGTGGTGGTGCGTGCCT TCCTGGCCAACATGGCTGTCTTTACTAAAAATGCAAAAATTAGCTGTGTGTGGTGGTGCGTGCCT A G PHACTR1 Ensembl:ENSG00000112137 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1035502795 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21632 5022 RMVar_ID_5022 Human_SNP_ID_267351888 A-to-I Human chr6 + 12895748 12895747 12895748 CATCAGAACTCTACGTATTGATTCTCGAGCCTAGCTGCAAATTAGCATTGCCTGCGGGAATTTCA CATCAGAACTCTACGTATTGATTCTCGAGCCT_GCTGCAAATTAGCATTGCCTGCGGGAATTTCA TA T PHACTR1 Ensembl:ENSG00000112137 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1267478709 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_21632 5023 RMVar_ID_5023 Human_SNP_ID_267361036 A-to-I Human chr6 + 12934796 12934796 12934796 AAGCAGAGGTTGCGGTGAGCCAAGATCATGCCACTACACTCCAGTCTAGGTGACAGAATGAGATC AAGCAGAGGTTGCGGTGAGCCAAGATCATGCCGCTACACTCCAGTCTAGGTGACAGAATGAGATC A G PHACTR1 Ensembl:ENSG00000112137 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1331941986 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21632 5024 RMVar_ID_5024 Human_SNP_ID_267362138 A-to-I Human chr6 + 12939798 12939798 12939798 TTTTCTGACATCCAGTCCAGAACTTTACCTCCAATGCCAAACTGTTTCTTGTTGATTGTTCAAGT TTTTCTGACATCCAGTCCAGAACTTTACCTCCTATGCCAAACTGTTTCTTGTTGATTGTTCAAGT A T PHACTR1 Ensembl:ENSG00000112137 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1381338183 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21632 5025 RMVar_ID_5025 Human_SNP_ID_267444602 A-to-I Human chr6 - 13291158 13291158 13291158 AAAAATAGCCAGGTGTGGTGGTGCACACCTCTAGTCACAGCTACCCGGGAGGCTGAGGCAGTAGA AAAAATAGCCAGGTGTGGTGGTGCACACCTCTCGTCACAGCTACCCGGGAGGCTGAGGCAGTAGA T G TBC1D7,AL008729.1 Ensembl:ENSG00000145979,Ensembl:ENSG00000215022 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1301462301 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118055,RMVar_hsa_circ_237192 5026 RMVar_ID_5026 Human_SNP_ID_267444878 A-to-I Human chr6 - 13292047 13292047 13292047 CCAGGAGGCAGAGGTTGCAGTGAGCTGAGATCATTCCACGGCACTCCAGCCTAGGAGACAGAGCA CCAGGAGGCAGAGGTTGCAGTGAGCTGAGATCGTTCCACGGCACTCCAGCCTAGGAGACAGAGCA T C TBC1D7,AL008729.1 Ensembl:ENSG00000145979,Ensembl:ENSG00000215022 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1345721943 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8271393 RMVar_hsa_circ_118055,RMVar_hsa_circ_237192 5027 RMVar_ID_5027 Human_SNP_ID_267450960 A-to-I Human chr6 - 13316679 13316679 13316679 CAGGAGCCAGATGATGAAGTGTTTCTTGCCATAGCTAAAGCCATGGAGGAAATGGTGGAAGATAG CAGGAGCCAGATGATGAAGTGTTTCTTGCCATCGCTAAAGCCATGGAGGAAATGGTGGAAGATAG T G TBC1D7 Ensembl:ENSG00000145979 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1368472866 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_653402,Human_RBP_ID_18084692,Human_RBP_ID_22460399 Human_Splice_Rec_739300,Human_Splice_Rec_739314,Human_Splice_Rec_739328,Human_Splice_Rec_739340,Human_Splice_Rec_739360,Human_Splice_Rec_739370,Human_Splice_Rec_739380,Human_Splice_Rec_739388,Human_Splice_Rec_739398,Human_Splice_Rec_739406,Human_Splice_Rec_739416,Human_Splice_Rec_739424,Human_Splice_Rec_739430,Human_Splice_Rec_739440,Human_Splice_Rec_739448,Human_Splice_Rec_739456 RMVar_hsa_circ_36441,RMVar_hsa_circ_118055,RMVar_hsa_circ_237192,RMVar_hsa_circ_285006,RMVar_hsa_circ_237196,RMVar_hsa_circ_237194,RMVar_hsa_circ_375816,RMVar_hsa_circ_68130,RMVar_hsa_circ_306522,RMVar_hsa_circ_237197 5028 RMVar_ID_5028 Human_SNP_ID_267518646 A-to-I Human chr6 + 13585059 13585059 13585059 AACAGAGGCCTCAGAAATAACACTACACATCTACAACCATCTGATCTTTGACAAACCTGACAAAA AACAGAGGCCTCAGAAATAACACTACACATCTGCAACCATCTGATCTTTGACAAACCTGACAAAA A G SIRT5 Ensembl:ENSG00000124523 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs916411421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_739536,Human_Splice_Rec_739537 RMVar_hsa_circ_16789,RMVar_hsa_circ_237202,RMVar_hsa_circ_273294,RMVar_hsa_circ_237199,RMVar_hsa_circ_277109,RMVar_hsa_circ_319128,RMVar_hsa_circ_354396,RMVar_hsa_circ_316855,RMVar_hsa_circ_276123,RMVar_hsa_circ_55375,RMVar_hsa_circ_237203,RMVar_hsa_circ_237204,RMVar_hsa_circ_237201,RMVar_hsa_circ_74769,RMVar_hsa_circ_237205 5029 RMVar_ID_5029 Human_SNP_ID_267518992 A-to-I Human chr6 + 13586564 13586564 13586564 CAAAGATCAGATGGTTGTAGATGTGTGGTGTTATTTCTGAGGCCTCTGTTCTGTTCCACCGTGAC CAAAGATCAGATGGTTGTAGATGTGTGGTGTTCTTTCTGAGGCCTCTGTTCTGTTCCACCGTGAC A C SIRT5 Ensembl:ENSG00000124523 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1012450188 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16789,RMVar_hsa_circ_237202,RMVar_hsa_circ_273294,RMVar_hsa_circ_237199,RMVar_hsa_circ_277109,RMVar_hsa_circ_319128,RMVar_hsa_circ_354396,RMVar_hsa_circ_316855,RMVar_hsa_circ_276123,RMVar_hsa_circ_237203,RMVar_hsa_circ_237204,RMVar_hsa_circ_237201,RMVar_hsa_circ_74769,RMVar_hsa_circ_237205 5030 RMVar_ID_5030 Human_SNP_ID_267521990 A-to-I Human chr6 + 13598667 13598667 13598667 GCCCGGCGAATGTGGTGAAACATGTCTCTACTAAGAATACGAAAATTAGCTGGGTGTGGTCACAC GCCCGGCGAATGTGGTGAAACATGTCTCTACTGAGAATACGAAAATTAGCTGGGTGTGGTCACAC A G SIRT5 Ensembl:ENSG00000124523 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1229051422 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16789,RMVar_hsa_circ_237199,RMVar_hsa_circ_277109,RMVar_hsa_circ_354396,RMVar_hsa_circ_237204,RMVar_hsa_circ_18688,RMVar_hsa_circ_237205,RMVar_hsa_circ_360533 5031 RMVar_ID_5031 Human_SNP_ID_267541046 A-to-I Human chr6 - 13669770 13669770 13669770 TGGGCAACATGGAGAAACCCTGTCTGTACAAAAAATGCGAAAAAAAGTTAGCCAGGCATGGTGGC TGGGCAACATGGAGAAACCCTGTCTGTACAAATAATGCGAAAAAAAGTTAGCCAGGCATGGTGGC T A RANBP9 Ensembl:ENSG00000010017 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1183549120 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81702,RMVar_hsa_circ_367336,RMVar_hsa_circ_237208,RMVar_hsa_circ_335565,RMVar_hsa_circ_237221,RMVar_hsa_circ_237222,RMVar_hsa_circ_41001,RMVar_hsa_circ_237231,RMVar_hsa_circ_237230,RMVar_hsa_circ_97913,RMVar_hsa_circ_280339,RMVar_hsa_circ_237233,RMVar_hsa_circ_375584,RMVar_hsa_circ_237234 5032 RMVar_ID_5032 Human_SNP_ID_267541047 A-to-I Human chr6 - 13669770 13669770 13669770 TGGGCAACATGGAGAAACCCTGTCTGTACAAAAAATGCGAAAAAAAGTTAGCCAGGCATGGTGGC TGGGCAACATGGAGAAACCCTGTCTGTACAAACAATGCGAAAAAAAGTTAGCCAGGCATGGTGGC T G RANBP9 Ensembl:ENSG00000010017 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1183549120 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81702,RMVar_hsa_circ_367336,RMVar_hsa_circ_237208,RMVar_hsa_circ_335565,RMVar_hsa_circ_237221,RMVar_hsa_circ_237222,RMVar_hsa_circ_41001,RMVar_hsa_circ_237231,RMVar_hsa_circ_237230,RMVar_hsa_circ_97913,RMVar_hsa_circ_280339,RMVar_hsa_circ_237233,RMVar_hsa_circ_375584,RMVar_hsa_circ_237234 5033 RMVar_ID_5033 Human_SNP_ID_267545388 A-to-I Human chr6 - 13686212 13686193 13686212 TGGTCCCAGCTATATGAGAGGCTGAGCCAGGAAGATCGCTTGAGCCCAGGAGGTCAAGGCTGCAG TGGTCCCAGCTATATGAGAGGCTGAGCCAGGA___________________GGTCAAGGCTGCAG CTCCTGGGCTCAAGCGATCT C RANBP9 Ensembl:ENSG00000010017 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202989171 Functional Loss DEL dbSNP153 33..51 33 - - - Human_RBP_ID_15660986 RMVar_hsa_circ_81702,RMVar_hsa_circ_367336,RMVar_hsa_circ_237208,RMVar_hsa_circ_335565,RMVar_hsa_circ_237221,RMVar_hsa_circ_237222,RMVar_hsa_circ_41001,RMVar_hsa_circ_237231,RMVar_hsa_circ_237230,RMVar_hsa_circ_97913,RMVar_hsa_circ_280339,RMVar_hsa_circ_375584,RMVar_hsa_circ_237234,RMVar_hsa_circ_237235 5034 RMVar_ID_5034 Human_SNP_ID_267546259 A-to-I Human chr6 - 13689399 13689399 13689399 GGGTGTGGTGGCACATGCCTGTAGTCACATCTACTTGGGGAGCCAAGGCAGAAGAATCGCTTGAA GGGTGTGGTGGCACATGCCTGTAGTCACATCTGCTTGGGGAGCCAAGGCAGAAGAATCGCTTGAA T C RANBP9 Ensembl:ENSG00000010017 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs948220124 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7547433,Human_RBP_ID_17576222 RMVar_hsa_circ_81702,RMVar_hsa_circ_367336,RMVar_hsa_circ_237208,RMVar_hsa_circ_335565,RMVar_hsa_circ_237221,RMVar_hsa_circ_237222,RMVar_hsa_circ_41001,RMVar_hsa_circ_237231,RMVar_hsa_circ_237230,RMVar_hsa_circ_97913,RMVar_hsa_circ_280339,RMVar_hsa_circ_375584,RMVar_hsa_circ_237234,RMVar_hsa_circ_237235 5035 RMVar_ID_5035 Human_SNP_ID_267573436 A-to-I Human chr6 - 13778016 13778016 13778016 GAAGGGAGTGTTATCGAGCCGAACTGGGGTCTACTTGCCCTGTGTAGTAAGGTCAAATATCTGTA GAAGGGAGTGTTATCGAGCCGAACTGGGGTCTGCTTGCCCTGTGTAGTAAGGTCAAATATCTGTA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1374754136 Functional Loss SNV dbSNP153 33..33 33 - - - 5036 RMVar_ID_5036 Human_SNP_ID_267575971 A-to-I Human chr6 - 13787813 13787813 13787813 CTACCCTGGCTTATAAGGATTCAGATTACTTTAGGAAATTAGGCATTAGCACTAGGAGGGGGGAA CTACCCTGGCTTATAAGGATTCAGATTACTTTGGGAAATTAGGCATTAGCACTAGGAGGGGGGAA T C MCUR1 Ensembl:ENSG00000050393 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11557522 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5151772,Human_RBP_ID_8896630,Human_RBP_ID_15662564,Human_RBP_ID_17304805,Human_RBP_ID_18366229,Human_RBP_ID_26539751,Human_RBP_ID_27750275 RMVar_hsa_circ_109132,RMVar_hsa_circ_237237 5037 RMVar_ID_5037 Human_SNP_ID_267576019 A-to-I Human chr6 - 13787979 13787979 13787979 ACTCGGGAGGCTGAGACAGGAAAATTGCATGAACCTGGGAGGCAGAGGTTGCAGTGAGCAGAGAT ACTCGGGAGGCTGAGACAGGAAAATTGCATGATCCTGGGAGGCAGAGGTTGCAGTGAGCAGAGAT T A MCUR1 Ensembl:ENSG00000050393 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1328895398 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109132,RMVar_hsa_circ_237237 5038 RMVar_ID_5038 Human_SNP_ID_267576022 A-to-I Human chr6 - 13787990 13787990 13787990 TAATCCTAGCTACTCGGGAGGCTGAGACAGGAAAATTGCATGAACCTGGGAGGCAGAGGTTGCAG TAATCCTAGCTACTCGGGAGGCTGAGACAGGAGAATTGCATGAACCTGGGAGGCAGAGGTTGCAG T C MCUR1 Ensembl:ENSG00000050393 Protein coding 3'UTR GSE47997;GSE107867;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;ASD brains,Fragile X samples from NIH NeuroBioBank;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,30559470,32596459,32596459 RNA-Seq:(High) rs1272696704 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109132,RMVar_hsa_circ_237237 5039 RMVar_ID_5039 Human_SNP_ID_267576058 A-to-I Human chr6 - 13788158 13788158 13788158 CTTACTGATGCTGGGTGCGGTGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCCAAGGCAGGC CTTACTGATGCTGGGTGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGC T C MCUR1 Ensembl:ENSG00000050393 Protein coding 3'UTR GSE38233;GSE99789;GSE112787;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;esophageal squamous carcinoma cells,EC109;293 Flip-In T-REx cells,empty vector;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29796672,29967493,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs529766945 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109132,RMVar_hsa_circ_237237 5040 RMVar_ID_5040 Human_SNP_ID_267576333 A-to-I Human chr6 - 13789159 13789159 13789159 TGACCTCGTGATTCACCCGCCTTGGTCTCCCAAAGTAGTGGGATTACAGGCGTGAGCCGCTGCGC TGACCTCGTGATTCACCCGCCTTGGTCTCCCAGAGTAGTGGGATTACAGGCGTGAGCCGCTGCGC T C MCUR1 Ensembl:ENSG00000050393 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,31158229,32596459 RNA-Seq:(High) rs955713756 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26539756 RMVar_hsa_circ_7100,RMVar_hsa_circ_109132,RMVar_hsa_circ_331721,RMVar_hsa_circ_237237,RMVar_hsa_circ_62883 5041 RMVar_ID_5041 Human_SNP_ID_267576358 A-to-I Human chr6 - 13789218 13789218 13789218 TTTTGTATTTTTAGTAGAGATGAGGTTTCACCATGTTGGCCAGGCTGGTCTCTAACTCCTGACCT TTTTGTATTTTTAGTAGAGATGAGGTTTCACCTTGTTGGCCAGGCTGGTCTCTAACTCCTGACCT T A MCUR1 Ensembl:ENSG00000050393 Protein coding 3'UTR GSE99789;GSE123020:GSM3490829,GSM3490830,GSM3490831 esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109 cell line - 29796672,32596459 RNA-Seq:(High) rs1364122930 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 5042 RMVar_ID_5042 Human_SNP_ID_267576359 A-to-I Human chr6 - 13789218 13789218 13789218 TTTTGTATTTTTAGTAGAGATGAGGTTTCACCATGTTGGCCAGGCTGGTCTCTAACTCCTGACCT TTTTGTATTTTTAGTAGAGATGAGGTTTCACCGTGTTGGCCAGGCTGGTCTCTAACTCCTGACCT T C MCUR1 Ensembl:ENSG00000050393 Protein coding 3'UTR GSE99789;GSE123020:GSM3490829,GSM3490830,GSM3490831 esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109 cell line - 29796672,32596459 RNA-Seq:(High) rs1364122930 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 5043 RMVar_ID_5043 Human_SNP_ID_267576726 A-to-I Human chr6 - 13790568 13790568 13790568 GGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTAAGGTGTGAACCTGGGAGGCGGAGCTTGTAGTG GGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGTGTGAACCTGGGAGGCGGAGCTTGTAGTG T C MCUR1 Ensembl:ENSG00000050393 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1561727889 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 5044 RMVar_ID_5044 Human_SNP_ID_267578617 A-to-I Human chr6 - 13797940 13797940 13797940 CTGCCCACTGCAACCTCCGTCTCCTGGGTTTAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCT CTGCCCACTGCAACCTCCGTCTCCTGGGTTTAGGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCT T C MCUR1 Ensembl:ENSG00000050393 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1051032657 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_237239,RMVar_hsa_circ_31490,RMVar_hsa_circ_109132,RMVar_hsa_circ_331721,RMVar_hsa_circ_237237,RMVar_hsa_circ_105164,RMVar_hsa_circ_302323,RMVar_hsa_circ_44117,RMVar_hsa_circ_27871,RMVar_hsa_circ_237240,RMVar_hsa_circ_237241,RMVar_hsa_circ_338080,RMVar_hsa_circ_237238,RMVar_hsa_circ_299118 5045 RMVar_ID_5045 Human_SNP_ID_704163097 A-to-I Human chr22 + 40048864 40048860 40048864 ATCCATCCATCCATCTTTCTTGTCTTTCTGACAGAGTTTCGCTCTGTCGCCCAGGCTGGAGTGAA ATCCATCCATCCATCTTTCTTGTCTTTCT____GAGTTTCGCTCTGTCGCCCAGGCTGGAGTGAA TGACA T TNRC6B Ensembl:ENSG00000100354 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1415284176 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_20781739 5046 RMVar_ID_5046 Human_SNP_ID_704163098 A-to-I Human chr22 + 40048864 40048863 40048865 ATCCATCCATCCATCTTTCTTGTCTTTCTGACAGAGTTTCGCTCTGTCGCCCAGGCTGGAGTGAA ATCCATCCATCCATCTTTCTTGTCTTTCTGAC__AGTTTCGCTCTGTCGCCCAGGCTGGAGTGAA CAG C TNRC6B Ensembl:ENSG00000100354 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978240398 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_20781739 5047 RMVar_ID_5047 Human_SNP_ID_704169505 A-to-I Human chr22 + 40073922 40073921 40073922 TCTACTAAAAACAAAAAACAATACAAAAAATTAGTCGGGCATGGTGGCGTGTGCCTGTAGTCCCA TCTACTAAAAACAAAAAACAATACAAAAAATT_GTCGGGCATGGTGGCGTGTGCCTGTAGTCCCA TA T TNRC6B Ensembl:ENSG00000100354 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1340904098 Functional Loss DEL dbSNP153 33..33 33 - - - 5048 RMVar_ID_5048 Human_SNP_ID_704169506 A-to-I Human chr22 + 40073922 40073922 40073922 TCTACTAAAAACAAAAAACAATACAAAAAATTAGTCGGGCATGGTGGCGTGTGCCTGTAGTCCCA TCTACTAAAAACAAAAAACAATACAAAAAATTTGTCGGGCATGGTGGCGTGTGCCTGTAGTCCCA A T TNRC6B Ensembl:ENSG00000100354 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1271893270 Functional Loss SNV dbSNP153 33..33 33 - - - 5049 RMVar_ID_5049 Human_SNP_ID_704176340 A-to-I Human chr22 + 40101215 40101204 40101215 GGGGTTTCATTGCGTTAGCCAGGATGGTCTCGATCTCCTAACCTTGTGATCCGCCCACCTCGGTC GGGGTTTCATTGCGTTAGCCAG___________TCTCCTAACCTTGTGATCCGCCCACCTCGGTC GGATGGTCTCGA G TNRC6B Ensembl:ENSG00000100354 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1447748202 Functional Loss DEL dbSNP153 23..33 33 - - - 5050 RMVar_ID_5050 Human_SNP_ID_704181600 A-to-I Human chr22 + 40124892 40124892 40124892 AAAATCGGCCGGGTGTGGTGGCAGGCGCCTGTAGTCCCAGCTACTTGGGAGACTGAGGCAGGAGC AAAATCGGCCGGGTGTGGTGGCAGGCGCCTGTGGTCCCAGCTACTTGGGAGACTGAGGCAGGAGC A G TNRC6B Ensembl:ENSG00000100354 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1449509355 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_214422,RMVar_hsa_circ_99177,RMVar_hsa_circ_272040,RMVar_hsa_circ_353382,RMVar_hsa_circ_271108,RMVar_hsa_circ_51529,RMVar_hsa_circ_76525,RMVar_hsa_circ_214424,RMVar_hsa_circ_214425,RMVar_hsa_circ_214423 5051 RMVar_ID_5051 Human_SNP_ID_704184797 A-to-I Human chr22 + 40136452 40136452 40136452 GCAGAGTGTTGCTCTGTCGCGTAGGCTGGAGTATAGTAGCCTGAACACAGCTCATTGCAGCCTGA GCAGAGTGTTGCTCTGTCGCGTAGGCTGGAGTGTAGTAGCCTGAACACAGCTCATTGCAGCCTGA A G TNRC6B Ensembl:ENSG00000100354 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1338917706 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 5052 RMVar_ID_5052 Human_SNP_ID_704189713 A-to-I Human chr22 + 40154077 40154077 40154077 GTGATCATAGAGCGCTACAGTCTTGAACTCCTAGGCTCAATTGATTCTCCTGCCTCTGTCCCCCG GTGATCATAGAGCGCTACAGTCTTGAACTCCTGGGCTCAATTGATTCTCCTGCCTCTGTCCCCCG A G TNRC6B Ensembl:ENSG00000100354 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1476313658 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 5053 RMVar_ID_5053 Human_SNP_ID_704196606 A-to-I Human chr22 - 40178095 40178095 40178095 GCAGTGCTTAAATCCAGCAAATTGAGGCATACAAGGTAGAAATGGAAATGAAAAAAGGTCCAAAA GCAGTGCTTAAATCCAGCAAATTGAGGCATACGAGGTAGAAATGGAAATGAAAAAAGGTCCAAAA T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1171255873 Functional Loss SNV dbSNP153 33..33 33 - - - 5054 RMVar_ID_5054 Human_SNP_ID_704197956 A-to-I Human chr22 + 40183886 40183886 40183886 CCAGCTAATTTTTTGTATATTTTAGTAGATACAGTGTTTCGGCATGTTGGCCAGGCTGATCTCGA CCAGCTAATTTTTTGTATATTTTAGTAGATACGGTGTTTCGGCATGTTGGCCAGGCTGATCTCGA A G TNRC6B Ensembl:ENSG00000100354 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968825792 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14492237 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 5055 RMVar_ID_5055 Human_SNP_ID_704197963 A-to-I Human chr22 + 40183912 40183912 40183912 AGATACAGTGTTTCGGCATGTTGGCCAGGCTGATCTCGAACTCCTGACCTTGTGATTCACCTGCC AGATACAGTGTTTCGGCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTTGTGATTCACCTGCC A G TNRC6B Ensembl:ENSG00000100354 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs963112902 Functional Loss SNV dbSNP153 33..33 33 - - - 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 5056 RMVar_ID_5056 Human_SNP_ID_704219238 A-to-I Human chr22 + 40268111 40268110 40268112 AATATTAAGAACCAGTTTTCTTTTTTTGAGACAGAGTCTCACTCTGTTGCCCAGGCTGGAGTGCA AATATTAAGAACCAGTTTTCTTTTTTTGAGAC__AGTCTCACTCTGTTGCCCAGGCTGGAGTGCA CAG C TNRC6B Ensembl:ENSG00000100354 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1487217728 Functional Loss DEL dbSNP153 33..34 33 - - - 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_361212,RMVar_hsa_circ_61821,RMVar_hsa_circ_354473,RMVar_hsa_circ_361202,RMVar_hsa_circ_214427,RMVar_hsa_circ_308738,RMVar_hsa_circ_268376,RMVar_hsa_circ_304472,RMVar_hsa_circ_331155,RMVar_hsa_circ_214430 5057 RMVar_ID_5057 Human_SNP_ID_704219277 A-to-I Human chr22 + 40268266 40268266 40268266 CACTGCCATGCCCAGCTAATGTTTGTATTTTTAGTAGAGACAGGATTTCACCATGTTGGCCAGGG CACTGCCATGCCCAGCTAATGTTTGTATTTTTCGTAGAGACAGGATTTCACCATGTTGGCCAGGG A C TNRC6B Ensembl:ENSG00000100354 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1372275192 Functional Loss SNV dbSNP153 33..33 33 - - - 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_361212,RMVar_hsa_circ_61821,RMVar_hsa_circ_354473,RMVar_hsa_circ_361202,RMVar_hsa_circ_214427,RMVar_hsa_circ_308738,RMVar_hsa_circ_268376,RMVar_hsa_circ_304472,RMVar_hsa_circ_331155,RMVar_hsa_circ_214430 5058 RMVar_ID_5058 Human_SNP_ID_704219282 A-to-I Human chr22 + 40268286 40268280 40268286 GTTTGTATTTTTAGTAGAGACAGGATTTCACCATGTTGGCCAGGGTGGTCTCAGACTCCTGACCT GTTTGTATTTTTAGTAGAGACAGGATT______TGTTGGCCAGGGTGGTCTCAGACTCCTGACCT TTCACCA T TNRC6B Ensembl:ENSG00000100354 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1171359205 Functional Loss DEL dbSNP153 28..33 33 - - - 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_361212,RMVar_hsa_circ_61821,RMVar_hsa_circ_354473,RMVar_hsa_circ_361202,RMVar_hsa_circ_214427,RMVar_hsa_circ_308738,RMVar_hsa_circ_268376,RMVar_hsa_circ_304472,RMVar_hsa_circ_331155,RMVar_hsa_circ_214430 5059 RMVar_ID_5059 Human_SNP_ID_704219285 A-to-I Human chr22 + 40268286 40268286 40268286 GTTTGTATTTTTAGTAGAGACAGGATTTCACCATGTTGGCCAGGGTGGTCTCAGACTCCTGACCT GTTTGTATTTTTAGTAGAGACAGGATTTCACCGTGTTGGCCAGGGTGGTCTCAGACTCCTGACCT A G TNRC6B Ensembl:ENSG00000100354 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs953475170 Functional Loss SNV dbSNP153 33..33 33 - - - 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_361212,RMVar_hsa_circ_61821,RMVar_hsa_circ_354473,RMVar_hsa_circ_361202,RMVar_hsa_circ_214427,RMVar_hsa_circ_308738,RMVar_hsa_circ_268376,RMVar_hsa_circ_304472,RMVar_hsa_circ_331155,RMVar_hsa_circ_214430 5060 RMVar_ID_5060 Human_SNP_ID_704219396 A-to-I Human chr22 + 40268723 40268723 40268723 CATGAGGTCAGGAGATCGAGACCATCTTGGCTAACACGGTGAAACCCCGCCTCTACTAAAAAATC CATGAGGTCAGGAGATCGAGACCATCTTGGCTGACACGGTGAAACCCCGCCTCTACTAAAAAATC A G TNRC6B Ensembl:ENSG00000100354 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1043074773 Functional Loss SNV dbSNP153 33..33 33 - - - 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_361212,RMVar_hsa_circ_61821,RMVar_hsa_circ_354473,RMVar_hsa_circ_361202,RMVar_hsa_circ_214427,RMVar_hsa_circ_308738,RMVar_hsa_circ_268376,RMVar_hsa_circ_304472,RMVar_hsa_circ_331155,RMVar_hsa_circ_214430 5061 RMVar_ID_5061 Human_SNP_ID_704236795 A-to-I Human chr22 - 40334776 40334776 40334776 CGTGGAGGGAGGAGGAGAGGAGGAAGGAAGCCACAAGTCACAAATAATTAAAATGGTACTTCTCT CGTGGAGGGAGGAGGAGAGGAGGAAGGAAGCCCCAAGTCACAAATAATTAAAATGGTACTTCTCT T G - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs554117565 Functional Loss SNV dbSNP153 33..33 33 - - - 5062 RMVar_ID_5062 Human_SNP_ID_704241402 A-to-I Human chr22 + 40351787 40351787 40351787 TGGAGTCTCCTGCCTCAGCCTTCCAAGTAGCTAGGACTACAGGCGCCCGCCACCACACCCGGCTA TGGAGTCTCCTGCCTCAGCCTTCCAAGTAGCTGGGACTACAGGCGCCCGCCACCACACCCGGCTA A G AL022238.4,ADSL Ensembl:ENSG00000284431,Ensembl:ENSG00000239900 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965188209 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3246,RMVar_hsa_circ_60997,RMVar_hsa_circ_97636,RMVar_hsa_circ_317233,RMVar_hsa_circ_214449,RMVar_hsa_circ_334311,RMVar_hsa_circ_40538,RMVar_hsa_circ_54088,RMVar_hsa_circ_24188,RMVar_hsa_circ_214451 5063 RMVar_ID_5063 Human_SNP_ID_704241512 A-to-I Human chr22 + 40352254 40352254 40352254 ACTGTAGGCAAGAAAAATGGGGGAGGCTGGGCACGGTGGCTCACACCTGTAATCCCAGCACTTTG ACTGTAGGCAAGAAAAATGGGGGAGGCTGGGCGCGGTGGCTCACACCTGTAATCCCAGCACTTTG A G AL022238.4,ADSL Ensembl:ENSG00000284431,Ensembl:ENSG00000239900 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs964200160 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3246,RMVar_hsa_circ_60997,RMVar_hsa_circ_97636,RMVar_hsa_circ_317233,RMVar_hsa_circ_214449,RMVar_hsa_circ_334311,RMVar_hsa_circ_40538,RMVar_hsa_circ_54088,RMVar_hsa_circ_24188,RMVar_hsa_circ_214451 5064 RMVar_ID_5064 Human_SNP_ID_704241593 A-to-I Human chr22 + 40352510 40352510 40352510 AGATCGCGCCACTGCACTACAGCCTGGGCGACAGAGCGAGACTCCCATCTTAAAAAGAAAAAAAA AGATCGCGCCACTGCACTACAGCCTGGGCGACGGAGCGAGACTCCCATCTTAAAAAGAAAAAAAA A G AL022238.4,ADSL Ensembl:ENSG00000284431,Ensembl:ENSG00000239900 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1373468003 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14494380 RMVar_hsa_circ_3246,RMVar_hsa_circ_60997,RMVar_hsa_circ_97636,RMVar_hsa_circ_317233,RMVar_hsa_circ_214449,RMVar_hsa_circ_334311,RMVar_hsa_circ_40538,RMVar_hsa_circ_54088,RMVar_hsa_circ_24188,RMVar_hsa_circ_214451 5065 RMVar_ID_5065 Human_SNP_ID_704242229 A-to-I Human chr22 + 40354748 40354748 40354748 CAAACATTAGCCAGATTTGGTAGCATGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA CAAACATTAGCCAGATTTGGTAGCATGCCTGTGATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA A G AL022238.4,ADSL Ensembl:ENSG00000284431,Ensembl:ENSG00000239900 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs902197133 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3246,RMVar_hsa_circ_60997,RMVar_hsa_circ_334311,RMVar_hsa_circ_40538,RMVar_hsa_circ_24188,RMVar_hsa_circ_214453,RMVar_hsa_circ_273800,RMVar_hsa_circ_281970,RMVar_hsa_circ_101403,RMVar_hsa_circ_103010,RMVar_hsa_circ_214455,RMVar_hsa_circ_214454,RMVar_hsa_circ_127303,RMVar_hsa_circ_330350,RMVar_hsa_circ_372080,RMVar_hsa_circ_214452,RMVar_hsa_circ_359917,RMVar_hsa_circ_292516,RMVar_hsa_circ_117076,RMVar_hsa_circ_214459,RMVar_hsa_circ_214460,RMVar_hsa_circ_214461,RMVar_hsa_circ_214458 5066 RMVar_ID_5066 Human_SNP_ID_704243127 A-to-I Human chr22 + 40357953 40357953 40357953 GCCACCACGCCCAGTTAATTTTTTGTATTTTTAGTAGAGACAGGGTTTTACCTGTCTCTGTTGGC GCCACCACGCCCAGTTAATTTTTTGTATTTTTTGTAGAGACAGGGTTTTACCTGTCTCTGTTGGC A T AL022238.4,ADSL Ensembl:ENSG00000284431,Ensembl:ENSG00000239900 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1169601078 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14494494 RMVar_hsa_circ_3246,RMVar_hsa_circ_60997,RMVar_hsa_circ_334311,RMVar_hsa_circ_40538,RMVar_hsa_circ_24188,RMVar_hsa_circ_214453,RMVar_hsa_circ_273800,RMVar_hsa_circ_281970,RMVar_hsa_circ_101403,RMVar_hsa_circ_103010,RMVar_hsa_circ_214455,RMVar_hsa_circ_214454,RMVar_hsa_circ_127303,RMVar_hsa_circ_330350,RMVar_hsa_circ_372080,RMVar_hsa_circ_214452,RMVar_hsa_circ_359917,RMVar_hsa_circ_292516,RMVar_hsa_circ_117076,RMVar_hsa_circ_214459,RMVar_hsa_circ_214460,RMVar_hsa_circ_214461,RMVar_hsa_circ_214458 5067 RMVar_ID_5067 Human_SNP_ID_704243250 A-to-I Human chr22 + 40358419 40358419 40358419 CAGCCTGAGCAACAAAGTGAGACCCCGTCACTACAAAAAATTTAAAAATTAGCCAGGCATGGTAT CAGCCTGAGCAACAAAGTGAGACCCCGTCACTGCAAAAAATTTAAAAATTAGCCAGGCATGGTAT A G AL022238.4,ADSL Ensembl:ENSG00000284431,Ensembl:ENSG00000239900 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1013149848 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14494517 RMVar_hsa_circ_3246,RMVar_hsa_circ_60997,RMVar_hsa_circ_334311,RMVar_hsa_circ_40538,RMVar_hsa_circ_24188,RMVar_hsa_circ_214453,RMVar_hsa_circ_273800,RMVar_hsa_circ_281970,RMVar_hsa_circ_101403,RMVar_hsa_circ_103010,RMVar_hsa_circ_214455,RMVar_hsa_circ_214454,RMVar_hsa_circ_127303,RMVar_hsa_circ_330350,RMVar_hsa_circ_372080,RMVar_hsa_circ_214452,RMVar_hsa_circ_359917,RMVar_hsa_circ_292516,RMVar_hsa_circ_117076,RMVar_hsa_circ_214459,RMVar_hsa_circ_214460,RMVar_hsa_circ_214461,RMVar_hsa_circ_214458 5068 RMVar_ID_5068 Human_SNP_ID_704245505 A-to-I Human chr22 + 40367195 40367195 40367195 GGCTTGCTCTGTCACCCAGACTAGAGTGCAGTAGCACAATCTTGGCTCACTGCAACCTCCGCCTC GGCTTGCTCTGTCACCCAGACTAGAGTGCAGTGGCACAATCTTGGCTCACTGCAACCTCCGCCTC A G AL022238.4,ADSL Ensembl:ENSG00000284431,Ensembl:ENSG00000239900 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1396977397 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3246,RMVar_hsa_circ_57881 5069 RMVar_ID_5069 Human_SNP_ID_704245565 A-to-I Human chr22 + 40367417 40367417 40367417 TCTCAGCCTCCCAAAGTTCTGGGATTATAGACATGAGCCACCACACCCAGCCTAATCTTGTTTTC TCTCAGCCTCCCAAAGTTCTGGGATTATAGACGTGAGCCACCACACCCAGCCTAATCTTGTTTTC A G AL022238.4,ADSL Ensembl:ENSG00000284431,Ensembl:ENSG00000239900 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1387510066 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3246,RMVar_hsa_circ_57881 5070 RMVar_ID_5070 Human_SNP_ID_704245567 A-to-I Human chr22 + 40367420 40367420 40367420 CAGCCTCCCAAAGTTCTGGGATTATAGACATGAGCCACCACACCCAGCCTAATCTTGTTTTCTTT CAGCCTCCCAAAGTTCTGGGATTATAGACATGCGCCACCACACCCAGCCTAATCTTGTTTTCTTT A C AL022238.4,ADSL Ensembl:ENSG00000284431,Ensembl:ENSG00000239900 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049597269 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3246,RMVar_hsa_circ_57881 5071 RMVar_ID_5071 Human_SNP_ID_704245895 A-to-I Human chr22 + 40368750 40368750 40368750 GGAGTTCGAGACCAGCTTGACCGACAAGGTGAAACTCCGTCTCTACTAAAAATACAATCAACCGG GGAGTTCGAGACCAGCTTGACCGACAAGGTGATACTCCGTCTCTACTAAAAATACAATCAACCGG A T AL022238.4,ADSL Ensembl:ENSG00000284431,Ensembl:ENSG00000239900 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1198921348 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3246,RMVar_hsa_circ_57881 5072 RMVar_ID_5072 Human_SNP_ID_704248981 A-to-I Human chr22 + 40380466 40380466 40380466 TCAGCTCACTGTAACCTCCGCCTCCCGGGTTCAAGCAATTCTCCCACCTCAGCATCCCGAGTAGT TCAGCTCACTGTAACCTCCGCCTCCCGGGTTCGAGCAATTCTCCCACCTCAGCATCCCGAGTAGT A G AL022238.4,ADSL,SGSM3 Ensembl:ENSG00000284431,Ensembl:ENSG00000239900,Ensembl:ENSG00000100359 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs565691259 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3246,RMVar_hsa_circ_57881,RMVar_hsa_circ_214472,RMVar_hsa_circ_114422 5073 RMVar_ID_5073 Human_SNP_ID_704249041 A-to-I Human chr22 + 40380729 40380729 40380729 AGGCCAAGGTAGGATGACTGATTGAGCCCAGGAATTTAAGACCAGCCTGGGCAACATAGTAAGAC AGGCCAAGGTAGGATGACTGATTGAGCCCAGGTATTTAAGACCAGCCTGGGCAACATAGTAAGAC A T AL022238.4,ADSL,SGSM3 Ensembl:ENSG00000284431,Ensembl:ENSG00000239900,Ensembl:ENSG00000100359 Protein coding,Protein coding,Protein coding intron,intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1286451143 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3246,RMVar_hsa_circ_57881,RMVar_hsa_circ_214472,RMVar_hsa_circ_114422 5074 RMVar_ID_5074 Human_SNP_ID_704252259 A-to-I Human chr22 + 40394632 40394632 40394632 GTGCCACTGCACTCTAGCCTGGGTGACAGAGTAAGACTCCTGTCTCAAAAAAAAAAAAAAAAAAA GTGCCACTGCACTCTAGCCTGGGTGACAGAGTGAGACTCCTGTCTCAAAAAAAAAAAAAAAAAAA A G AL022238.4,SGSM3 Ensembl:ENSG00000284431,Ensembl:ENSG00000100359 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1400480597 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3246,RMVar_hsa_circ_57881,RMVar_hsa_circ_214472,RMVar_hsa_circ_114422 5075 RMVar_ID_5075 Human_SNP_ID_704253746 A-to-I Human chr22 - 40400664 40400664 40400664 CCTGTTAGAAGAGAAAAGAGGAAAGTCATTCTATTTTTATTTTTATTTTTTTTTAGACAGAGTCT CCTGTTAGAAGAGAAAAGAGGAAAGTCATTCTGTTTTTATTTTTATTTTTTTTTAGACAGAGTCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1488781092 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7095929 5076 RMVar_ID_5076 Human_SNP_ID_704275859 A-to-I Human chr22 - 40476671 40476671 40476671 CGGTGGGTGGATCATTTGAGCCCAGGAGTTCAAGACTAGCCTGGGCAACAGGCGAAACCCTGTCT CGGTGGGTGGATCATTTGAGCCCAGGAGTTCAGGACTAGCCTGGGCAACAGGCGAAACCCTGTCT T C MRTFA Ensembl:ENSG00000196588 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1369586110 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 5077 RMVar_ID_5077 Human_SNP_ID_704277560 A-to-I Human chr22 - 40483442 40483442 40483442 TGACCTCGTGATCCACTCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCATTGCGC TGACCTCGTGATCCACTCGCCTCGGCCTCCCAGAGTGCTGGGATTACAGGCGTGAGCCATTGCGC T C MRTFA Ensembl:ENSG00000196588 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1450378782 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 5078 RMVar_ID_5078 Human_SNP_ID_704277683 A-to-I Human chr22 - 40483833 40483833 40483833 AAAATTGGTCAAGCATGCTACTGTGCGTCTGTAGTCCCGATTACTCAGGAGGCTGAGGTGGGAGG AAAATTGGTCAAGCATGCTACTGTGCGTCTGTCGTCCCGATTACTCAGGAGGCTGAGGTGGGAGG T G MRTFA Ensembl:ENSG00000196588 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs938433433 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 5079 RMVar_ID_5079 Human_SNP_ID_704277718 A-to-I Human chr22 - 40483973 40483973 40483973 CATGCCCAATCCCAGCAAAGCCTGTAATCCCAACATTTTGGGAGGTTGAGGTGAGCGGATCACTT CATGCCCAATCCCAGCAAAGCCTGTAATCCCAGCATTTTGGGAGGTTGAGGTGAGCGGATCACTT T C MRTFA Ensembl:ENSG00000196588 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444213838 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 5080 RMVar_ID_5080 Human_SNP_ID_704281462 A-to-I Human chr22 - 40498423 40498423 40498423 AAAAATCAGCTGGGCATGGTAGCTTGTACCTTAGTCCCCGCTACTTGGGAGGCTGAGGTGAGAGG AAAAATCAGCTGGGCATGGTAGCTTGTACCTTGGTCCCCGCTACTTGGGAGGCTGAGGTGAGAGG T C MRTFA Ensembl:ENSG00000196588 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900247001 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 5081 RMVar_ID_5081 Human_SNP_ID_704285819 A-to-I Human chr22 - 40514752 40514752 40514752 GGAAGGGCTGGGCGTGGTGGCTCACATCTGTAATCTCAGCACTTTGGGAGGCCGAAGCGGGTGGA GGAAGGGCTGGGCGTGGTGGCTCACATCTGTAGTCTCAGCACTTTGGGAGGCCGAAGCGGGTGGA T C MRTFA Ensembl:ENSG00000196588 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1445298285 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 5082 RMVar_ID_5082 Human_SNP_ID_704286406 A-to-I Human chr22 - 40517122 40517122 40517122 GTCCAGGAGCTCTAGAACAGCCTGGGCAACATAGTGAGACTGCCATTTCTACAAATAATGAAAAA GTCCAGGAGCTCTAGAACAGCCTGGGCAACATTGTGAGACTGCCATTTCTACAAATAATGAAAAA T A MRTFA Ensembl:ENSG00000196588 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1258497739 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14496915 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 5083 RMVar_ID_5083 Human_SNP_ID_704286413 A-to-I Human chr22 - 40517150 40517150 40517150 GGGATGCCAAGGCAGGAGGATTGCTTGAGTCCAGGAGCTCTAGAACAGCCTGGGCAACATAGTGA GGGATGCCAAGGCAGGAGGATTGCTTGAGTCCGGGAGCTCTAGAACAGCCTGGGCAACATAGTGA T C MRTFA Ensembl:ENSG00000196588 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006323934 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17572827 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 5084 RMVar_ID_5084 Human_SNP_ID_704289800 A-to-I Human chr22 - 40530425 40530425 40530425 AGGTGTGGTGGTGCATGTCTGTAGTCCCAGCTACTTGGGGGGCTGAGGCAGGAGAATTGCTTGAA AGGTGTGGTGGTGCATGTCTGTAGTCCCAGCTGCTTGGGGGGCTGAGGCAGGAGAATTGCTTGAA T C MRTFA Ensembl:ENSG00000196588 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1297557879 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 5085 RMVar_ID_5085 Human_SNP_ID_704289991 A-to-I Human chr22 - 40531237 40531237 40531237 AAAAAAAGCCAGGTATGATGGTGCCCACCTGTAGTCAGAGCTACTTGGGAAGCTGAGGTGGGAGG AAAAAAAGCCAGGTATGATGGTGCCCACCTGTTGTCAGAGCTACTTGGGAAGCTGAGGTGGGAGG T A MRTFA Ensembl:ENSG00000196588 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355591375 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14497382 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 5086 RMVar_ID_5086 Human_SNP_ID_704292762 A-to-I Human chr22 - 40540555 40540555 40540555 GGTTGGTCTCGAACCCCTGATCCACCCACCTCAGCCTCTCAAAGTGCTGGAATTACAGGTTTGAG GGTTGGTCTCGAACCCCTGATCCACCCACCTCGGCCTCTCAAAGTGCTGGAATTACAGGTTTGAG T C MRTFA Ensembl:ENSG00000196588 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1233084669 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 5087 RMVar_ID_5087 Human_SNP_ID_704293784 A-to-I Human chr22 - 40544919 40544919 40544919 ATTTATTTATTTATTTATTTATTTTTCAAGACAGTGTCATGCTCTGTTGCCTAGGCTGGAGGATA ATTTATTTATTTATTTATTTATTTTTCAAGACGGTGTCATGCTCTGTTGCCTAGGCTGGAGGATA T C MRTFA Ensembl:ENSG00000196588 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs554661064 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2719641,Human_RBP_ID_7095951,Human_RBP_ID_14497641 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 5088 RMVar_ID_5088 Human_SNP_ID_704293785 A-to-I Human chr22 - 40544919 40544919 40544919 ATTTATTTATTTATTTATTTATTTTTCAAGACAGTGTCATGCTCTGTTGCCTAGGCTGGAGGATA ATTTATTTATTTATTTATTTATTTTTCAAGACCGTGTCATGCTCTGTTGCCTAGGCTGGAGGATA T G MRTFA Ensembl:ENSG00000196588 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs554661064 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2719641,Human_RBP_ID_7095951,Human_RBP_ID_14497641 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 5089 RMVar_ID_5089 Human_SNP_ID_704294814 A-to-I Human chr22 - 40548849 40548849 40548849 GTGGTATATATATATTTTTGAGACAGAGTCTCACTCTGTTGCCAGGCTGGAGTGCAGTGGCGCGA GTGGTATATATATATTTTTGAGACAGAGTCTCGCTCTGTTGCCAGGCTGGAGTGCAGTGGCGCGA T C MRTFA Ensembl:ENSG00000196588 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256607105 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 5090 RMVar_ID_5090 Human_SNP_ID_704295040 A-to-I Human chr22 - 40549962 40549962 40549962 TCACTGCAGCCTCCGTCTCCCGGGTTCAAGCAATTCTCTTGCCTCAGCCACCCGAGTAGCTGGGA TCACTGCAGCCTCCGTCTCCCGGGTTCAAGCAGTTCTCTTGCCTCAGCCACCCGAGTAGCTGGGA T C MRTFA Ensembl:ENSG00000196588 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs950107861 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 5091 RMVar_ID_5091 Human_SNP_ID_704301427 A-to-I Human chr22 - 40576058 40576058 40576058 TGCCACTGTACTCCAGCCTGGGAGACAGAACAAGACTCCGTCTCAAAAAAAAAAAAAAAAAAGAA TGCCACTGTACTCCAGCCTGGGAGACAGAACAGGACTCCGTCTCAAAAAAAAAAAAAAAAAAGAA T C MRTFA Ensembl:ENSG00000196588 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs567105595 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80394,RMVar_hsa_circ_89916,RMVar_hsa_circ_214485,RMVar_hsa_circ_214486,RMVar_hsa_circ_214488,RMVar_hsa_circ_123843,RMVar_hsa_circ_347051,RMVar_hsa_circ_214495,RMVar_hsa_circ_272139 5092 RMVar_ID_5092 Human_SNP_ID_704301720 A-to-I Human chr22 - 40577222 40577221 40577222 TTTTTTTTTTTTTTTTTTTAGACAAGGGTCTTACTCTGTTACTCAGGCAGGAGTGCATGAGTGCA TTTTTTTTTTTTTTTTTTTAGACAAGGGTCTT_CTCTGTTACTCAGGCAGGAGTGCATGAGTGCA GT G MRTFA Ensembl:ENSG00000196588 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1252382978 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_80394,RMVar_hsa_circ_89916,RMVar_hsa_circ_214485,RMVar_hsa_circ_214486,RMVar_hsa_circ_214488,RMVar_hsa_circ_123843,RMVar_hsa_circ_347051,RMVar_hsa_circ_214495,RMVar_hsa_circ_272139 5093 RMVar_ID_5093 Human_SNP_ID_704301723 A-to-I Human chr22 - 40577222 40577222 40577222 TTTTTTTTTTTTTTTTTTTAGACAAGGGTCTTACTCTGTTACTCAGGCAGGAGTGCATGAGTGCA TTTTTTTTTTTTTTTTTTTAGACAAGGGTCTTGCTCTGTTACTCAGGCAGGAGTGCATGAGTGCA T C MRTFA Ensembl:ENSG00000196588 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1282326414 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80394,RMVar_hsa_circ_89916,RMVar_hsa_circ_214485,RMVar_hsa_circ_214486,RMVar_hsa_circ_214488,RMVar_hsa_circ_123843,RMVar_hsa_circ_347051,RMVar_hsa_circ_214495,RMVar_hsa_circ_272139 5094 RMVar_ID_5094 Human_SNP_ID_704304582 A-to-I Human chr22 - 40588964 40588964 40588964 TTTTTTTTTCCCCTGAGACAAGGTCTTACTCTATTGCCCCAGGCTGGAATGCAGTGGCGCAATCA TTTTTTTTTCCCCTGAGACAAGGTCTTACTCTGTTGCCCCAGGCTGGAATGCAGTGGCGCAATCA T C MRTFA Ensembl:ENSG00000196588 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs751903676 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2719735,Human_RBP_ID_25672761 RMVar_hsa_circ_80394,RMVar_hsa_circ_89916,RMVar_hsa_circ_214485,RMVar_hsa_circ_214486,RMVar_hsa_circ_214488,RMVar_hsa_circ_123843,RMVar_hsa_circ_347051,RMVar_hsa_circ_214495,RMVar_hsa_circ_272139,RMVar_hsa_circ_214496 5095 RMVar_ID_5095 Human_SNP_ID_704305565 A-to-I Human chr22 - 40592645 40592645 40592645 CTACAAAAAACACCAAAAAAAATTAGCCAGGCATGGTGACATGTGCCTGTAGTCCCATTTGCTAG CTACAAAAAACACCAAAAAAAATTAGCCAGGCGTGGTGACATGTGCCTGTAGTCCCATTTGCTAG T C MRTFA Ensembl:ENSG00000196588 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1378661092 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80394,RMVar_hsa_circ_89916,RMVar_hsa_circ_214485,RMVar_hsa_circ_214486,RMVar_hsa_circ_214488,RMVar_hsa_circ_123843,RMVar_hsa_circ_347051,RMVar_hsa_circ_214495,RMVar_hsa_circ_272139,RMVar_hsa_circ_214496 5096 RMVar_ID_5096 Human_SNP_ID_704310380 A-to-I Human chr22 - 40612765 40612765 40612765 TAAACATTGTTTTGTAGAGACAGAGCCTTACTATGTTGTCCGGGCTGGTATCAAACTCCTAGCCT TAAACATTGTTTTGTAGAGACAGAGCCTTACTGTGTTGTCCGGGCTGGTATCAAACTCCTAGCCT T C MRTFA Ensembl:ENSG00000196588 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs551676017 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14498542 5097 RMVar_ID_5097 Human_SNP_ID_704315072 A-to-I Human chr22 - 40630795 40630795 40630795 GAGAGGCTGAGACAGGAGGATTGCTTGAGCCCAGGAGTTTGAGGCTGCAATGAGCTGTGATCACA GAGAGGCTGAGACAGGAGGATTGCTTGAGCCCGGGAGTTTGAGGCTGCAATGAGCTGTGATCACA T C MRTFA Ensembl:ENSG00000196588 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs774518415 Functional Loss SNV dbSNP153 33..33 33 - - - 5098 RMVar_ID_5098 Human_SNP_ID_704315101 A-to-I Human chr22 - 40630930 40630930 40630930 AAGAGCTAGGGCCCATAATAAAAATACCTAGAATGAGAACCTGTGTGGCTGAGTTTGAGGGACAA AAGAGCTAGGGCCCATAATAAAAATACCTAGAGTGAGAACCTGTGTGGCTGAGTTTGAGGGACAA T C MRTFA Ensembl:ENSG00000196588 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs536567129 Functional Loss SNV dbSNP153 33..33 33 - - - 5099 RMVar_ID_5099 Human_SNP_ID_704322318 A-to-I Human chr22 + 40658822 40658822 40658822 TGCCCGGCTAATTTTTTATTTTTCGTAGAGACAAGGTCTTACTATGTTGCCCACGCTGGTCTTGA TGCCCGGCTAATTTTTTATTTTTCGTAGAGACGAGGTCTTACTATGTTGCCCACGCTGGTCTTGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1023500277 Functional Loss SNV dbSNP153 33..33 33 - - - 5100 RMVar_ID_5100 Human_SNP_ID_704343795 A-to-I Human chr22 - 40740398 40740398 40740398 GCACTCCAGGCTGGGCAATAAGAAAGAAACTCAGTCTGGAAAAAAAAAAAAAGACGTTTGCTTTG GCACTCCAGGCTGGGCAATAAGAAAGAAACTCCGTCTGGAAAAAAAAAAAAAGACGTTTGCTTTG T G lnc-SLC25A17-4 RNACentral:URS0000D5C0C4 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917047295 Functional Loss SNV dbSNP153 33..33 33 - - - 5101 RMVar_ID_5101 Human_SNP_ID_704344073 A-to-I Human chr22 - 40741631 40741631 40741631 ACCTCAAGTGATCCACTTGCCTTAGCCTTGTAAAGTGCTAGGATTACAGGCGTGAGCCCCGTGCC ACCTCAAGTGATCCACTTGCCTTAGCCTTGTAGAGTGCTAGGATTACAGGCGTGAGCCCCGTGCC T C lnc-SLC25A17-4 RNACentral:URS0000D5C0C4 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs945675262 Functional Loss SNV dbSNP153 33..33 33 - - - 5102 RMVar_ID_5102 Human_SNP_ID_704344274 A-to-I Human chr22 - 40742318 40742318 40742318 CTTCTGCCTCAGCCCCCTGAGTAGCTGGGACTACAGGCACCCGCCACCATGCCCAGCTAATTTTT CTTCTGCCTCAGCCCCCTGAGTAGCTGGGACTGCAGGCACCCGCCACCATGCCCAGCTAATTTTT T C lnc-SLC25A17-4 RNACentral:URS0000D5C0C4 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs566103851 Functional Loss SNV dbSNP153 33..33 33 - - - 5103 RMVar_ID_5103 Human_SNP_ID_704344276 A-to-I Human chr22 - 40742328 40742328 40742328 TCACGCCGTTCTTCTGCCTCAGCCCCCTGAGTAGCTGGGACTACAGGCACCCGCCACCATGCCCA TCACGCCGTTCTTCTGCCTCAGCCCCCTGAGTGGCTGGGACTACAGGCACCCGCCACCATGCCCA T C lnc-SLC25A17-4 RNACentral:URS0000D5C0C4 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs533346069 Functional Loss SNV dbSNP153 33..33 33 - - - 5104 RMVar_ID_5104 Human_SNP_ID_704344292 A-to-I Human chr22 - 40742377 40742377 40742377 GGAGTGCAGTGGTGCAATCTCCGCTCACTGCAAGCTCTGCCTCCCGGGTTCACGCCGTTCTTCTG GGAGTGCAGTGGTGCAATCTCCGCTCACTGCAGGCTCTGCCTCCCGGGTTCACGCCGTTCTTCTG T C lnc-SLC25A17-4 RNACentral:URS0000D5C0C4 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs377168738 Functional Loss SNV dbSNP153 33..33 33 - - - 5105 RMVar_ID_5105 Human_SNP_ID_704344463 A-to-I Human chr22 - 40742966 40742966 40742966 ACTCGGGACGCTGAGGCAGGAGAATCATTTGAACCTGGGAGATGGAGGTTGCAGTGAGCTGTGAT ACTCGGGACGCTGAGGCAGGAGAATCATTTGAGCCTGGGAGATGGAGGTTGCAGTGAGCTGTGAT T C lnc-SLC25A17-4 RNACentral:URS0000D5C0C4 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs567553562 Functional Loss SNV dbSNP153 33..33 33 - - - 5106 RMVar_ID_5106 Human_SNP_ID_704344471 A-to-I Human chr22 - 40742998 40742998 40742998 AGGCATAGTGGCAGGTGCCTGTAATCCCAGCTACTCGGGACGCTGAGGCAGGAGAATCATTTGAA AGGCATAGTGGCAGGTGCCTGTAATCCCAGCTGCTCGGGACGCTGAGGCAGGAGAATCATTTGAA T C lnc-SLC25A17-4 RNACentral:URS0000D5C0C4 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1438015596 Functional Loss SNV dbSNP153 33..33 33 - - - 5107 RMVar_ID_5107 Human_SNP_ID_704344489 A-to-I Human chr22 - 40743030 40743030 40743030 CCCCATTTGTACTAAAAATACAAAAATTAGCCAGGCATAGTGGCAGGTGCCTGTAATCCCAGCTA CCCCATTTGTACTAAAAATACAAAAATTAGCCGGGCATAGTGGCAGGTGCCTGTAATCCCAGCTA T C lnc-SLC25A17-4 RNACentral:URS0000D5C0C4 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs371168913 Functional Loss SNV dbSNP153 33..33 33 - - - 5108 RMVar_ID_5108 Human_SNP_ID_704344514 A-to-I Human chr22 - 40743073 40743073 40743073 TTGAGGTCAGGGGTTCGAGATCAGCCTGGCCAACATGATGAAACCCCATTTGTACTAAAAATACA TTGAGGTCAGGGGTTCGAGATCAGCCTGGCCAGCATGATGAAACCCCATTTGTACTAAAAATACA T C lnc-SLC25A17-4 RNACentral:URS0000D5C0C4 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs368494241 Functional Loss SNV dbSNP153 33..33 33 - - - 5109 RMVar_ID_5109 Human_SNP_ID_704344623 A-to-I Human chr22 - 40743495 40743495 40743495 TGAACTCCTGACCTCAACTGATCACCCGCCTCAGCCTCCTAAAGTGCTAAGATAGCCACGGTGCC TGAACTCCTGACCTCAACTGATCACCCGCCTCGGCCTCCTAAAGTGCTAAGATAGCCACGGTGCC T C lnc-SLC25A17-4 RNACentral:URS0000D5C0C4 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs371773532 Functional Loss SNV dbSNP153 33..33 33 - - - 5110 RMVar_ID_5110 Human_SNP_ID_704344648 A-to-I Human chr22 - 40743567 40743567 40743567 GGGTCACACCACTGTGCCCGGCTAATTTTTGTATTTTTTGTAGAGACAGGGTTTTCACCATCAGG GGGTCACACCACTGTGCCCGGCTAATTTTTGTGTTTTTTGTAGAGACAGGGTTTTCACCATCAGG T C lnc-SLC25A17-4 RNACentral:URS0000D5C0C4 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904679863 Functional Loss SNV dbSNP153 33..33 33 - - - 5111 RMVar_ID_5111 Human_SNP_ID_704344651 A-to-I Human chr22 - 40743576 40743576 40743576 GGGATTACAGGGTCACACCACTGTGCCCGGCTAATTTTTGTATTTTTTGTAGAGACAGGGTTTTC GGGATTACAGGGTCACACCACTGTGCCCGGCTGATTTTTGTATTTTTTGTAGAGACAGGGTTTTC T C lnc-SLC25A17-4 RNACentral:URS0000D5C0C4 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs376702454 Functional Loss SNV dbSNP153 33..33 33 - - - 5112 RMVar_ID_5112 Human_SNP_ID_704344661 A-to-I Human chr22 - 40743602 40743602 40743602 TTCATGCCTCAGCCTCCCCAGTATCTGGGATTACAGGGTCACACCACTGTGCCCGGCTAATTTTT TTCATGCCTCAGCCTCCCCAGTATCTGGGATTGCAGGGTCACACCACTGTGCCCGGCTAATTTTT T C lnc-SLC25A17-4 RNACentral:URS0000D5C0C4 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs370040695 Functional Loss SNV dbSNP153 33..33 33 - - - 5113 RMVar_ID_5113 Human_SNP_ID_704353635 A-to-I Human chr22 - 40780919 40780919 40780919 GTGATCCTCCCATATCAGCCTCTCAAAGTGCTAAGATTACAGGCATGAGCCACCACACTGGGCAT GTGATCCTCCCATATCAGCCTCTCAAAGTGCTGAGATTACAGGCATGAGCCACCACACTGGGCAT T C SLC25A17 Ensembl:ENSG00000100372 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1300344305 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39961,RMVar_hsa_circ_214499,RMVar_hsa_circ_275168,RMVar_hsa_circ_214500,RMVar_hsa_circ_214504,RMVar_hsa_circ_294085,RMVar_hsa_circ_307594,RMVar_hsa_circ_289744,RMVar_hsa_circ_214502,RMVar_hsa_circ_214503,RMVar_hsa_circ_329245,RMVar_hsa_circ_311156,RMVar_hsa_circ_214505 5114 RMVar_ID_5114 Human_SNP_ID_704354352 A-to-I Human chr22 - 40783888 40783888 40783888 CAACCTGGCCAACATGGCGAAACCCCCTGTCTACTAAAAATACAAAAATTAACTGGGTGTGGTAG CAACCTGGCCAACATGGCGAAACCCCCTGTCTGCTAAAAATACAAAAATTAACTGGGTGTGGTAG T C SLC25A17 Ensembl:ENSG00000100372 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1441943047 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39961,RMVar_hsa_circ_214499,RMVar_hsa_circ_275168,RMVar_hsa_circ_214500,RMVar_hsa_circ_214504,RMVar_hsa_circ_294085,RMVar_hsa_circ_307594,RMVar_hsa_circ_289744,RMVar_hsa_circ_214502,RMVar_hsa_circ_214503,RMVar_hsa_circ_329245,RMVar_hsa_circ_311156,RMVar_hsa_circ_214505 5115 RMVar_ID_5115 Human_SNP_ID_704358347 A-to-I Human chr22 - 40800477 40800477 40800477 GGAAAATTGCTTGAGCCCAGGAGTTCAAGGTTACAGTGAACTATGATCTCGCCACTGCACTGGAG GGAAAATTGCTTGAGCCCAGGAGTTCAAGGTTGCAGTGAACTATGATCTCGCCACTGCACTGGAG T C SLC25A17 Ensembl:ENSG00000100372 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1052257504 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14499560 5116 RMVar_ID_5116 Human_SNP_ID_704358364 A-to-I Human chr22 - 40800563 40800562 40800563 AGTGAGACTCTGTCTTTACAAAAAATAAAATTATCTGGGTGTGGTGACACACATCTGTAGTCCTA AGTGAGACTCTGTCTTTACAAAAAATAAAATT_TCTGGGTGTGGTGACACACATCTGTAGTCCTA AT A SLC25A17 Ensembl:ENSG00000100372 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904818254 Functional Loss DEL dbSNP153 33..33 33 - - - 5117 RMVar_ID_5117 Human_SNP_ID_704358771 A-to-I Human chr22 - 40801929 40801929 40801929 AAAATTAGCTGGGCATGGAGGCGGGCGCCCTTAATCCCAGCTACTCGGGAGGCTGAGACAGGAGA AAAATTAGCTGGGCATGGAGGCGGGCGCCCTTTATCCCAGCTACTCGGGAGGCTGAGACAGGAGA T A SLC25A17 Ensembl:ENSG00000100372 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs767558298 Functional Loss SNV dbSNP153 33..33 33 - - - 5118 RMVar_ID_5118 Human_SNP_ID_704358883 A-to-I Human chr22 - 40802479 40802479 40802479 CACCACGCCTGGCTAAGTTTTGTATTTTTAGTAGAGGGGGAGTTTCACCATGTTGGCCAGGCTGG CACCACGCCTGGCTAAGTTTTGTATTTTTAGTGGAGGGGGAGTTTCACCATGTTGGCCAGGCTGG T C SLC25A17 Ensembl:ENSG00000100372 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900529743 Functional Loss SNV dbSNP153 33..33 33 - - - 5119 RMVar_ID_5119 Human_SNP_ID_704360450 A-to-I Human chr22 - 40809545 40809545 40809545 TTACTGTAGCCCCAACAGCCCAGGCTCAAGCAATTCTCCCACTTCAGCTTCCCAAGTAGCTGGGA TTACTGTAGCCCCAACAGCCCAGGCTCAAGCATTTCTCCCACTTCAGCTTCCCAAGTAGCTGGGA T A SLC25A17 Ensembl:ENSG00000100372 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs761737881 Functional Loss SNV dbSNP153 33..33 33 - - - 5120 RMVar_ID_5120 Human_SNP_ID_704360451 A-to-I Human chr22 - 40809545 40809545 40809545 TTACTGTAGCCCCAACAGCCCAGGCTCAAGCAATTCTCCCACTTCAGCTTCCCAAGTAGCTGGGA TTACTGTAGCCCCAACAGCCCAGGCTCAAGCAGTTCTCCCACTTCAGCTTCCCAAGTAGCTGGGA T C SLC25A17 Ensembl:ENSG00000100372 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs761737881 Functional Loss SNV dbSNP153 33..33 33 - - - 5121 RMVar_ID_5121 Human_SNP_ID_704360452 A-to-I Human chr22 - 40809545 40809545 40809545 TTACTGTAGCCCCAACAGCCCAGGCTCAAGCAATTCTCCCACTTCAGCTTCCCAAGTAGCTGGGA TTACTGTAGCCCCAACAGCCCAGGCTCAAGCACTTCTCCCACTTCAGCTTCCCAAGTAGCTGGGA T G SLC25A17 Ensembl:ENSG00000100372 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs761737881 Functional Loss SNV dbSNP153 33..33 33 - - - 5122 RMVar_ID_5122 Human_SNP_ID_704360460 A-to-I Human chr22 - 40809585 40809585 40809585 ACTGTGTACCCAGGCTGGAGTGCAGTGGCACAATCTCAGCTTACTGTAGCCCCAACAGCCCAGGC ACTGTGTACCCAGGCTGGAGTGCAGTGGCACAGTCTCAGCTTACTGTAGCCCCAACAGCCCAGGC T C SLC25A17 Ensembl:ENSG00000100372 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs796330889 Functional Loss SNV dbSNP153 33..33 33 - - - 5123 RMVar_ID_5123 Human_SNP_ID_704362349 A-to-I Human chr22 - 40816790 40816790 40816790 CCTGGCTAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAAGTAGCCAGGCATGGTGGTGG CCTGGCTAACATGGTGAAACCCCGTCTCTACTTAAAATACAAAAAGTAGCCAGGCATGGTGGTGG T A SLC25A17 Ensembl:ENSG00000100372 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs961793359 Functional Loss SNV dbSNP153 33..33 33 - - - 5124 RMVar_ID_5124 Human_SNP_ID_704362357 A-to-I Human chr22 - 40816804 40816804 40816804 GAGTTCGAGGCCAGCCTGGCTAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAAGTAGCC GAGTTCGAGGCCAGCCTGGCTAACATGGTGAAGCCCCGTCTCTACTAAAAATACAAAAAGTAGCC T C SLC25A17 Ensembl:ENSG00000100372 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs923446610 Functional Loss SNV dbSNP153 33..33 33 - - - 5125 RMVar_ID_5125 Human_SNP_ID_704371015 A-to-I Human chr22 - 40846215 40846213 40846215 AGGTATGCCTGAGGTCAGGCACGGTGACTCACACCTTTAATCCCAGCACTTTGGGAGGCTGAGGC AGGTATGCCTGAGGTCAGGCACGGTGACTCAC__CTTTAATCCCAGCACTTTGGGAGGCTGAGGC GGT G ST13 Ensembl:ENSG00000100380 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs562156277 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_59280,RMVar_hsa_circ_354126,RMVar_hsa_circ_378365,RMVar_hsa_circ_214510,RMVar_hsa_circ_306891,RMVar_hsa_circ_288392,RMVar_hsa_circ_214511,RMVar_hsa_circ_327098,RMVar_hsa_circ_359540,RMVar_hsa_circ_214512 5126 RMVar_ID_5126 Human_SNP_ID_704371754 A-to-I Human chr22 - 40848550 40848550 40848550 AGTAGAGATGGTTTCACCGTGTTGGCCAGGCTAGTCTTGAACTCCTAACCTCAAATGATCCACCC AGTAGAGATGGTTTCACCGTGTTGGCCAGGCTGGTCTTGAACTCCTAACCTCAAATGATCCACCC T C ST13 Ensembl:ENSG00000100380 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1368839598 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14500728 RMVar_hsa_circ_59280,RMVar_hsa_circ_306891,RMVar_hsa_circ_31572,RMVar_hsa_circ_288392,RMVar_hsa_circ_214511,RMVar_hsa_circ_327098 5127 RMVar_ID_5127 Human_SNP_ID_704377903 A-to-I Human chr22 + 40868772 40868772 40868772 GGAGGCTTGAGGCAGGAGAATCACTTGAACCCAGGAGGTGGAGGTTGCAGTGAGCCGAGATCATG GGAGGCTTGAGGCAGGAGAATCACTTGAACCCGGGAGGTGGAGGTTGCAGTGAGCCGAGATCATG A G XPNPEP3 Ensembl:ENSG00000196236 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1030292777 Functional Loss SNV dbSNP153 33..33 33 - - - 5128 RMVar_ID_5128 Human_SNP_ID_704379538 A-to-I Human chr22 + 40875245 40875245 40875245 TCTCCCAGGCTAAACTGCAGCGGCATGATCATATCTCACTGCAGTCTCGACCTCCCAAGCGATCC TCTCCCAGGCTAAACTGCAGCGGCATGATCATTTCTCACTGCAGTCTCGACCTCCCAAGCGATCC A T XPNPEP3 Ensembl:ENSG00000196236 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1413544333 Functional Loss SNV dbSNP153 33..33 33 - - - 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 5129 RMVar_ID_5129 Human_SNP_ID_704379551 A-to-I Human chr22 + 40875282 40875282 40875282 ACTGCAGTCTCGACCTCCCAAGCGATCCTCCCACTTCAGTTTCCCAAGTAGCTAGGACTACAGGC ACTGCAGTCTCGACCTCCCAAGCGATCCTCCCGCTTCAGTTTCCCAAGTAGCTAGGACTACAGGC A G XPNPEP3 Ensembl:ENSG00000196236 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs773513707 Functional Loss SNV dbSNP153 33..33 33 - - - 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 5130 RMVar_ID_5130 Human_SNP_ID_704381524 A-to-I Human chr22 + 40883373 40883373 40883373 TATACAGTTGAGTTCTTTTTTTGTTTTTTTTTAGGCAGGGTCTCACTCTGTCACCCAGGTTGGGA TATACAGTTGAGTTCTTTTTTTGTTTTTTTTTGGGCAGGGTCTCACTCTGTCACCCAGGTTGGGA A G XPNPEP3 Ensembl:ENSG00000196236 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs977000494 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7085493 RMVar_hsa_circ_284435,RMVar_hsa_circ_356905,RMVar_hsa_circ_368796,RMVar_hsa_circ_310423,RMVar_hsa_circ_214515,RMVar_hsa_circ_214516,RMVar_hsa_circ_214518,RMVar_hsa_circ_83622,RMVar_hsa_circ_269191,RMVar_hsa_circ_278374,RMVar_hsa_circ_126281,RMVar_hsa_circ_214519,RMVar_hsa_circ_214517 5131 RMVar_ID_5131 Human_SNP_ID_704381525 A-to-I Human chr22 + 40883373 40883373 40883373 TATACAGTTGAGTTCTTTTTTTGTTTTTTTTTAGGCAGGGTCTCACTCTGTCACCCAGGTTGGGA TATACAGTTGAGTTCTTTTTTTGTTTTTTTTTTGGCAGGGTCTCACTCTGTCACCCAGGTTGGGA A T XPNPEP3 Ensembl:ENSG00000196236 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs977000494 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7085493 RMVar_hsa_circ_284435,RMVar_hsa_circ_356905,RMVar_hsa_circ_368796,RMVar_hsa_circ_310423,RMVar_hsa_circ_214515,RMVar_hsa_circ_214516,RMVar_hsa_circ_214518,RMVar_hsa_circ_83622,RMVar_hsa_circ_269191,RMVar_hsa_circ_278374,RMVar_hsa_circ_126281,RMVar_hsa_circ_214519,RMVar_hsa_circ_214517 5132 RMVar_ID_5132 Human_SNP_ID_704381889 A-to-I Human chr22 + 40884813 40884813 40884813 TTCGGGAGGCCAAGGGAGGTGGATTGCCTGAGATCAGGAGTTCGAGACCAGTCTGGACAACATGG TTCGGGAGGCCAAGGGAGGTGGATTGCCTGAGGTCAGGAGTTCGAGACCAGTCTGGACAACATGG A G XPNPEP3 Ensembl:ENSG00000196236 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1314773294 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_284435,RMVar_hsa_circ_356905,RMVar_hsa_circ_368796,RMVar_hsa_circ_310423,RMVar_hsa_circ_214515,RMVar_hsa_circ_214516,RMVar_hsa_circ_214518,RMVar_hsa_circ_83622,RMVar_hsa_circ_269191,RMVar_hsa_circ_278374,RMVar_hsa_circ_126281,RMVar_hsa_circ_214519,RMVar_hsa_circ_214517 5133 RMVar_ID_5133 Human_SNP_ID_704382845 A-to-I Human chr22 + 40888408 40888408 40888408 TGGGACCATTGGTGCATGCCACTATGCCTGCTAATTTTTTAAATTTTTTGTAGAGACAGGGTTTC TGGGACCATTGGTGCATGCCACTATGCCTGCTGATTTTTTAAATTTTTTGTAGAGACAGGGTTTC A G XPNPEP3 Ensembl:ENSG00000196236 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1351269986 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_356905,RMVar_hsa_circ_368796,RMVar_hsa_circ_310423,RMVar_hsa_circ_214516,RMVar_hsa_circ_214518,RMVar_hsa_circ_83622,RMVar_hsa_circ_269191,RMVar_hsa_circ_126281,RMVar_hsa_circ_329800,RMVar_hsa_circ_214517,RMVar_hsa_circ_284460,RMVar_hsa_circ_214523 5134 RMVar_ID_5134 Human_SNP_ID_704382858 A-to-I Human chr22 + 40888458 40888458 40888458 TAGAGACAGGGTTTCTCAGTGTTGTCCAGGCTAGTCTCGAACTCCTGAGCTCAAGCAGTCCGCCC TAGAGACAGGGTTTCTCAGTGTTGTCCAGGCTGGTCTCGAACTCCTGAGCTCAAGCAGTCCGCCC A G XPNPEP3 Ensembl:ENSG00000196236 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs17849444 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_356905,RMVar_hsa_circ_368796,RMVar_hsa_circ_310423,RMVar_hsa_circ_214516,RMVar_hsa_circ_214518,RMVar_hsa_circ_83622,RMVar_hsa_circ_269191,RMVar_hsa_circ_126281,RMVar_hsa_circ_329800,RMVar_hsa_circ_214517,RMVar_hsa_circ_284460,RMVar_hsa_circ_214523 5135 RMVar_ID_5135 Human_SNP_ID_704382864 A-to-I Human chr22 + 40888478 40888478 40888478 GTTGTCCAGGCTAGTCTCGAACTCCTGAGCTCAAGCAGTCCGCCCACCTTGACCTCCCAAAGTGC GTTGTCCAGGCTAGTCTCGAACTCCTGAGCTCCAGCAGTCCGCCCACCTTGACCTCCCAAAGTGC A C XPNPEP3 Ensembl:ENSG00000196236 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1179475457 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_356905,RMVar_hsa_circ_368796,RMVar_hsa_circ_310423,RMVar_hsa_circ_214516,RMVar_hsa_circ_214518,RMVar_hsa_circ_83622,RMVar_hsa_circ_269191,RMVar_hsa_circ_126281,RMVar_hsa_circ_329800,RMVar_hsa_circ_214517,RMVar_hsa_circ_284460,RMVar_hsa_circ_214523 5136 RMVar_ID_5136 Human_SNP_ID_704382873 A-to-I Human chr22 + 40888491 40888488 40888491 GTCTCGAACTCCTGAGCTCAAGCAGTCCGCCCACCTTGACCTCCCAAAGTGCTGGGATTACAGGT GTCTCGAACTCCTGAGCTCAAGCAGTCCGC___CCTTGACCTCCCAAAGTGCTGGGATTACAGGT CCCA C XPNPEP3 Ensembl:ENSG00000196236 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749860803 Functional Loss DEL dbSNP153 31..33 33 - - - RMVar_hsa_circ_356905,RMVar_hsa_circ_368796,RMVar_hsa_circ_310423,RMVar_hsa_circ_214516,RMVar_hsa_circ_214518,RMVar_hsa_circ_83622,RMVar_hsa_circ_269191,RMVar_hsa_circ_126281,RMVar_hsa_circ_329800,RMVar_hsa_circ_214517,RMVar_hsa_circ_284460,RMVar_hsa_circ_214523 5137 RMVar_ID_5137 Human_SNP_ID_704383056 A-to-I Human chr22 + 40889160 40889160 40889160 TTAGGGGATACTCTTGCCTCAGCCTCCTGAGTAGCTTGGATTACAGGCACATACCACCATGGCTG TTAGGGGATACTCTTGCCTCAGCCTCCTGAGTGGCTTGGATTACAGGCACATACCACCATGGCTG A G XPNPEP3 Ensembl:ENSG00000196236 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1303882014 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_356905,RMVar_hsa_circ_368796,RMVar_hsa_circ_310423,RMVar_hsa_circ_214516,RMVar_hsa_circ_214518,RMVar_hsa_circ_83622,RMVar_hsa_circ_269191,RMVar_hsa_circ_126281,RMVar_hsa_circ_329800,RMVar_hsa_circ_214517,RMVar_hsa_circ_284460,RMVar_hsa_circ_214523 5138 RMVar_ID_5138 Human_SNP_ID_704384208 A-to-I Human chr22 + 40893796 40893794 40893796 GTGCCACTACGCCTGGCTAATTTTGTATTTTTAGTAGAGACGAGGTTTCTCCATATTGGTCAGGC GTGCCACTACGCCTGGCTAATTTTGTATTTT__GTAGAGACGAGGTTTCTCCATATTGGTCAGGC TTA T XPNPEP3 Ensembl:ENSG00000196236 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1311056154 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_356905,RMVar_hsa_circ_368796,RMVar_hsa_circ_310423,RMVar_hsa_circ_214516,RMVar_hsa_circ_214518,RMVar_hsa_circ_83622,RMVar_hsa_circ_269191,RMVar_hsa_circ_126281,RMVar_hsa_circ_329800,RMVar_hsa_circ_214517,RMVar_hsa_circ_284460,RMVar_hsa_circ_214523 5139 RMVar_ID_5139 Human_SNP_ID_704384209 A-to-I Human chr22 + 40893796 40893796 40893796 GTGCCACTACGCCTGGCTAATTTTGTATTTTTAGTAGAGACGAGGTTTCTCCATATTGGTCAGGC GTGCCACTACGCCTGGCTAATTTTGTATTTTTGGTAGAGACGAGGTTTCTCCATATTGGTCAGGC A G XPNPEP3 Ensembl:ENSG00000196236 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1163881135 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_356905,RMVar_hsa_circ_368796,RMVar_hsa_circ_310423,RMVar_hsa_circ_214516,RMVar_hsa_circ_214518,RMVar_hsa_circ_83622,RMVar_hsa_circ_269191,RMVar_hsa_circ_126281,RMVar_hsa_circ_329800,RMVar_hsa_circ_214517,RMVar_hsa_circ_284460,RMVar_hsa_circ_214523 5140 RMVar_ID_5140 Human_SNP_ID_704389635 A-to-I Human chr22 + 40914686 40914686 40914686 TCCTGAAGTGATCCTCTCTTCTCAGACCTCTTAAGTAGCTGGGACTATAGGCACATTGCCACCAT TCCTGAAGTGATCCTCTCTTCTCAGACCTCTTGAGTAGCTGGGACTATAGGCACATTGCCACCAT A G XPNPEP3 Ensembl:ENSG00000196236 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1293765002 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49896,RMVar_hsa_circ_356905,RMVar_hsa_circ_214518,RMVar_hsa_circ_83622,RMVar_hsa_circ_269191,RMVar_hsa_circ_126281,RMVar_hsa_circ_214517,RMVar_hsa_circ_363382,RMVar_hsa_circ_98365,RMVar_hsa_circ_214526,RMVar_hsa_circ_214527,RMVar_hsa_circ_299464,RMVar_hsa_circ_214528 5141 RMVar_ID_5141 Human_SNP_ID_704389783 A-to-I Human chr22 + 40915190 40915190 40915190 TCTCCTGCTTCAGCCTCCCGAGTAGCGGGACTACAGGCACCCACCACCACGCCTGGCTAATTTTT TCTCCTGCTTCAGCCTCCCGAGTAGCGGGACTGCAGGCACCCACCACCACGCCTGGCTAATTTTT A G XPNPEP3 Ensembl:ENSG00000196236 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1042488151 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49896,RMVar_hsa_circ_356905,RMVar_hsa_circ_214518,RMVar_hsa_circ_83622,RMVar_hsa_circ_269191,RMVar_hsa_circ_126281,RMVar_hsa_circ_214517,RMVar_hsa_circ_363382,RMVar_hsa_circ_98365,RMVar_hsa_circ_214526,RMVar_hsa_circ_214527,RMVar_hsa_circ_299464,RMVar_hsa_circ_214528 5142 RMVar_ID_5142 Human_SNP_ID_704389847 A-to-I Human chr22 + 40915502 40915502 40915502 TTGAACCCAGGGGACGGAAGTTGCAGTGAGCTAAGATTGGACTCTGCACTCCAGCCTGGGTGACA TTGAACCCAGGGGACGGAAGTTGCAGTGAGCTGAGATTGGACTCTGCACTCCAGCCTGGGTGACA A G XPNPEP3 Ensembl:ENSG00000196236 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1367630323 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49896,RMVar_hsa_circ_356905,RMVar_hsa_circ_214518,RMVar_hsa_circ_83622,RMVar_hsa_circ_269191,RMVar_hsa_circ_126281,RMVar_hsa_circ_214517,RMVar_hsa_circ_363382,RMVar_hsa_circ_98365,RMVar_hsa_circ_214526,RMVar_hsa_circ_214527,RMVar_hsa_circ_299464,RMVar_hsa_circ_214528 5143 RMVar_ID_5143 Human_SNP_ID_704390004 A-to-I Human chr22 + 40916171 40916171 40916171 AAAATTAGCTGAGTGTGGTGGCGGGCACCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAAT AAAATTAGCTGAGTGTGGTGGCGGGCACCTGTTATCCCAGCTACTCGGGAGGCTGAGGCAGGAAT A T XPNPEP3 Ensembl:ENSG00000196236 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1323919007 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49896,RMVar_hsa_circ_356905,RMVar_hsa_circ_214518,RMVar_hsa_circ_83622,RMVar_hsa_circ_269191,RMVar_hsa_circ_126281,RMVar_hsa_circ_214517,RMVar_hsa_circ_363382,RMVar_hsa_circ_98365,RMVar_hsa_circ_214526,RMVar_hsa_circ_214527,RMVar_hsa_circ_299464,RMVar_hsa_circ_214528 5144 RMVar_ID_5144 Human_SNP_ID_704390780 A-to-I Human chr22 + 40919548 40919548 40919548 CACCATGCCTGGCTAATATTTTGTTTTTTTGTAGAGACACGGTTTCGCTATGTTGCCCAGGCTGG CACCATGCCTGGCTAATATTTTGTTTTTTTGTGGAGACACGGTTTCGCTATGTTGCCCAGGCTGG A G XPNPEP3 Ensembl:ENSG00000196236 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1340369343 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49896,RMVar_hsa_circ_356905,RMVar_hsa_circ_214518,RMVar_hsa_circ_83622,RMVar_hsa_circ_269191,RMVar_hsa_circ_126281,RMVar_hsa_circ_214517,RMVar_hsa_circ_363382,RMVar_hsa_circ_98365,RMVar_hsa_circ_214526,RMVar_hsa_circ_214527,RMVar_hsa_circ_299464,RMVar_hsa_circ_214528 5145 RMVar_ID_5145 Human_SNP_ID_704392539 A-to-I Human chr22 + 40927201 40927201 40927201 ATATACTAAAGATCCAGACATCAGGGCTGGGCACAGCGGTTCCGCCTGTAATCCCAGCACTTTGG ATATACTAAAGATCCAGACATCAGGGCTGGGCCCAGCGGTTCCGCCTGTAATCCCAGCACTTTGG A C XPNPEP3 Ensembl:ENSG00000196236 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1418793483 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21896576 RMVar_hsa_circ_214518,RMVar_hsa_circ_83622,RMVar_hsa_circ_269191,RMVar_hsa_circ_126281,RMVar_hsa_circ_214517,RMVar_hsa_circ_98365,RMVar_hsa_circ_214526,RMVar_hsa_circ_214527 5146 RMVar_ID_5146 Human_SNP_ID_704392540 A-to-I Human chr22 + 40927203 40927203 40927203 ATACTAAAGATCCAGACATCAGGGCTGGGCACAGCGGTTCCGCCTGTAATCCCAGCACTTTGGGA ATACTAAAGATCCAGACATCAGGGCTGGGCACGGCGGTTCCGCCTGTAATCCCAGCACTTTGGGA A G XPNPEP3 Ensembl:ENSG00000196236 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs3200561 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21896576 RMVar_hsa_circ_214518,RMVar_hsa_circ_83622,RMVar_hsa_circ_269191,RMVar_hsa_circ_126281,RMVar_hsa_circ_214517,RMVar_hsa_circ_98365,RMVar_hsa_circ_214526,RMVar_hsa_circ_214527 5147 RMVar_ID_5147 Human_SNP_ID_704392550 A-to-I Human chr22 + 40927245 40927245 40927245 CCTGTAATCCCAGCACTTTGGGAGGTCCAGGCAGGTGGATCTCTTGAGACCAGGAGGTCAAGACC CCTGTAATCCCAGCACTTTGGGAGGTCCAGGCGGGTGGATCTCTTGAGACCAGGAGGTCAAGACC A G XPNPEP3 Ensembl:ENSG00000196236 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs3200563 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23949623 Human_miRNA_ID_2781916,Human_miRNA_ID_2787478 RMVar_hsa_circ_214518,RMVar_hsa_circ_83622,RMVar_hsa_circ_269191,RMVar_hsa_circ_126281,RMVar_hsa_circ_214517,RMVar_hsa_circ_98365,RMVar_hsa_circ_214526,RMVar_hsa_circ_214527 5148 RMVar_ID_5148 Human_SNP_ID_704392552 A-to-I Human chr22 + 40927264 40927264 40927264 GGGAGGTCCAGGCAGGTGGATCTCTTGAGACCAGGAGGTCAAGACCAGCCTGGCCAACGTGGTGA GGGAGGTCCAGGCAGGTGGATCTCTTGAGACCGGGAGGTCAAGACCAGCCTGGCCAACGTGGTGA A G XPNPEP3 Ensembl:ENSG00000196236 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1136921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23949623 Human_miRNA_ID_255022 RMVar_hsa_circ_214518,RMVar_hsa_circ_83622,RMVar_hsa_circ_269191,RMVar_hsa_circ_126281,RMVar_hsa_circ_214517,RMVar_hsa_circ_98365,RMVar_hsa_circ_214526,RMVar_hsa_circ_214527 5149 RMVar_ID_5149 Human_SNP_ID_704392553 A-to-I Human chr22 + 40927272 40927272 40927272 CAGGCAGGTGGATCTCTTGAGACCAGGAGGTCAAGACCAGCCTGGCCAACGTGGTGAAACACTGT CAGGCAGGTGGATCTCTTGAGACCAGGAGGTCGAGACCAGCCTGGCCAACGTGGTGAAACACTGT A G XPNPEP3 Ensembl:ENSG00000196236 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs926533871 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23949623 Human_miRNA_ID_468933,Human_miRNA_ID_607082,Human_miRNA_ID_1265638 RMVar_hsa_circ_214518,RMVar_hsa_circ_83622,RMVar_hsa_circ_269191,RMVar_hsa_circ_126281,RMVar_hsa_circ_214517,RMVar_hsa_circ_98365,RMVar_hsa_circ_214526,RMVar_hsa_circ_214527 5150 RMVar_ID_5150 Human_SNP_ID_704392560 A-to-I Human chr22 + 40927296 40927296 40927296 AGGAGGTCAAGACCAGCCTGGCCAACGTGGTGAAACACTGTCTCTACTAAAAATACAAAAATGAG AGGAGGTCAAGACCAGCCTGGCCAACGTGGTGGAACACTGTCTCTACTAAAAATACAAAAATGAG A G XPNPEP3 Ensembl:ENSG00000196236 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs3180260 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_498974,Human_miRNA_ID_2172678 RMVar_hsa_circ_214518,RMVar_hsa_circ_83622,RMVar_hsa_circ_269191,RMVar_hsa_circ_126281,RMVar_hsa_circ_214517,RMVar_hsa_circ_98365,RMVar_hsa_circ_214526,RMVar_hsa_circ_214527 5151 RMVar_ID_5151 Human_SNP_ID_704392565 A-to-I Human chr22 + 40927312 40927312 40927312 CCTGGCCAACGTGGTGAAACACTGTCTCTACTAAAAATACAAAAATGAGCTGGGTGTGATGATAC CCTGGCCAACGTGGTGAAACACTGTCTCTACTGAAAATACAAAAATGAGCTGGGTGTGATGATAC A G XPNPEP3 Ensembl:ENSG00000196236 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs5995966 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_33 RMVar_hsa_circ_214518,RMVar_hsa_circ_83622,RMVar_hsa_circ_269191,RMVar_hsa_circ_126281,RMVar_hsa_circ_214517,RMVar_hsa_circ_98365,RMVar_hsa_circ_214526,RMVar_hsa_circ_214527 5152 RMVar_ID_5152 Human_SNP_ID_704392578 A-to-I Human chr22 + 40927363 40927363 40927363 GGGTGTGATGATACATGCCTGTAATCCTGGCTACTTGGGAGGCTGAGGCATGAGAATTGCTTGAA GGGTGTGATGATACATGCCTGTAATCCTGGCTGCTTGGGAGGCTGAGGCATGAGAATTGCTTGAA A G XPNPEP3 Ensembl:ENSG00000196236 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1136926 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_214518,RMVar_hsa_circ_83622,RMVar_hsa_circ_269191,RMVar_hsa_circ_126281,RMVar_hsa_circ_214517,RMVar_hsa_circ_98365,RMVar_hsa_circ_214526,RMVar_hsa_circ_214527 5153 RMVar_ID_5153 Human_SNP_ID_704392597 A-to-I Human chr22 + 40927461 40927461 40927461 ATGCGACTGCACTCCAGCCTGGGTGACTGAGCAAGACTCTGCCTCAAAAAAACAAATAAATAAAT ATGCGACTGCACTCCAGCCTGGGTGACTGAGCGAGACTCTGCCTCAAAAAAACAAATAAATAAAT A G XPNPEP3 Ensembl:ENSG00000196236 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1379320224 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7085533 RMVar_hsa_circ_214518,RMVar_hsa_circ_83622,RMVar_hsa_circ_269191,RMVar_hsa_circ_126281,RMVar_hsa_circ_214517,RMVar_hsa_circ_98365,RMVar_hsa_circ_214526,RMVar_hsa_circ_214527 5154 RMVar_ID_5154 Human_SNP_ID_704392670 A-to-I Human chr22 + 40927764 40927764 40927764 GGGCGTGGTGGCGGATGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATGGCGTGAA GGGCGTGGTGGCGGATGCCTGTAGTCCCAGCTGCTCAGGAGGCTGAGGCAGGAGAATGGCGTGAA A G XPNPEP3 Ensembl:ENSG00000196236 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs3179547 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_214518,RMVar_hsa_circ_83622,RMVar_hsa_circ_269191,RMVar_hsa_circ_126281,RMVar_hsa_circ_214517,RMVar_hsa_circ_98365,RMVar_hsa_circ_214526,RMVar_hsa_circ_214527 5155 RMVar_ID_5155 Human_SNP_ID_704392873 A-to-I Human chr22 + 40928284 40928284 40928284 GATGGAGTGCAGTGGCGTAATCTCAGCTCACTACAACCTCCACCACCTGGGTTCAGGCAATTCTC GATGGAGTGCAGTGGCGTAATCTCAGCTCACTGCAACCTCCACCACCTGGGTTCAGGCAATTCTC A G XPNPEP3 Ensembl:ENSG00000196236 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs890095197 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_214518,RMVar_hsa_circ_83622,RMVar_hsa_circ_269191,RMVar_hsa_circ_126281,RMVar_hsa_circ_214517,RMVar_hsa_circ_98365,RMVar_hsa_circ_214526,RMVar_hsa_circ_214527 5156 RMVar_ID_5156 Human_SNP_ID_704392892 A-to-I Human chr22 + 40928372 40928372 40928372 GGGACTACAGGTGCACGCTGCCATGCCCAGCTAATTTTTTGTATTTTAGTAGAGACAGGGTTTCA GGGACTACAGGTGCACGCTGCCATGCCCAGCTTATTTTTTGTATTTTAGTAGAGACAGGGTTTCA A T XPNPEP3 Ensembl:ENSG00000196236 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1045729219 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_214518,RMVar_hsa_circ_83622,RMVar_hsa_circ_269191,RMVar_hsa_circ_126281,RMVar_hsa_circ_214517,RMVar_hsa_circ_98365,RMVar_hsa_circ_214526,RMVar_hsa_circ_214527 5157 RMVar_ID_5157 Human_SNP_ID_704392914 A-to-I Human chr22 + 40928475 40928475 40928475 GCAATCCGCCCACCTCAGCCTCCCAAAGTGCTAGGATTACAGGCATGAGCCACTGCGCCCGGTGT GCAATCCGCCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGCGCCCGGTGT A G XPNPEP3 Ensembl:ENSG00000196236 Protein coding 3'UTR GSE47997;GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 23474544,29129909,31158229 RNA-Seq:(High) rs1323943163 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_214518,RMVar_hsa_circ_83622,RMVar_hsa_circ_269191,RMVar_hsa_circ_126281,RMVar_hsa_circ_214517,RMVar_hsa_circ_98365,RMVar_hsa_circ_214526,RMVar_hsa_circ_214527 5158 RMVar_ID_5158 Human_SNP_ID_704393107 A-to-I Human chr22 + 40929223 40929223 40929223 TCTTTTTTTTTTTTTTTTTGAGACGGAGTCTCACACTGTCACCGGGGCTGGTGTGCAATAGCGAG TCTTTTTTTTTTTTTTTTTGAGACGGAGTCTCGCACTGTCACCGGGGCTGGTGTGCAATAGCGAG A G XPNPEP3 Ensembl:ENSG00000196236 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1471747954 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7085545 Human_miRNA_ID_2878381 RMVar_hsa_circ_214518,RMVar_hsa_circ_83622,RMVar_hsa_circ_269191,RMVar_hsa_circ_126281,RMVar_hsa_circ_214517,RMVar_hsa_circ_98365,RMVar_hsa_circ_214526,RMVar_hsa_circ_214527 5159 RMVar_ID_5159 Human_SNP_ID_704393120 A-to-I Human chr22 + 40929291 40929291 40929291 TCAGCTCCCTGCAACCTCCATCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAATAGC TCAGCTCCCTGCAACCTCCATCTCCCAGGTTCGAGCGATTCTCCTGCCTCAGCCTCCCGAATAGC A G XPNPEP3 Ensembl:ENSG00000196236 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1284135887 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_152452 RMVar_hsa_circ_214518,RMVar_hsa_circ_83622,RMVar_hsa_circ_269191,RMVar_hsa_circ_126281,RMVar_hsa_circ_214517,RMVar_hsa_circ_98365,RMVar_hsa_circ_214526,RMVar_hsa_circ_214527 5160 RMVar_ID_5160 Human_SNP_ID_704393146 A-to-I Human chr22 + 40929372 40929372 40929372 TGCCACCACACCCGGCTATTTTTTTGTATTTTAAATAGAGACGAGGTTTCACTGTGTTGGCCAGG TGCCACCACACCCGGCTATTTTTTTGTATTTTTAATAGAGACGAGGTTTCACTGTGTTGGCCAGG A T XPNPEP3 Ensembl:ENSG00000196236 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1217327028 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_214518,RMVar_hsa_circ_83622,RMVar_hsa_circ_269191,RMVar_hsa_circ_126281,RMVar_hsa_circ_214517,RMVar_hsa_circ_98365,RMVar_hsa_circ_214526,RMVar_hsa_circ_214527 5161 RMVar_ID_5161 Human_SNP_ID_704393166 A-to-I Human chr22 + 40929427 40929427 40929427 GTTGGCCAGGCTGGTCTCGAACTCCTGACCTCATGATCTGCCCGCCTCGGCCTCCCTAAGTGCTG GTTGGCCAGGCTGGTCTCGAACTCCTGACCTCGTGATCTGCCCGCCTCGGCCTCCCTAAGTGCTG A G XPNPEP3 Ensembl:ENSG00000196236 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs979112771 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_214518,RMVar_hsa_circ_83622,RMVar_hsa_circ_269191,RMVar_hsa_circ_126281,RMVar_hsa_circ_214517,RMVar_hsa_circ_98365,RMVar_hsa_circ_214526,RMVar_hsa_circ_214527 5162 RMVar_ID_5162 Human_SNP_ID_704393362 A-to-I Human chr22 + 40930204 40930204 40930204 CAGGCTGGAGTGCAGTGGCACGATCTTGGCTCACTGCAACCTCCATCTCCCGGGTTCAGGCAATT CAGGCTGGAGTGCAGTGGCACGATCTTGGCTCTCTGCAACCTCCATCTCCCGGGTTCAGGCAATT A T XPNPEP3 Ensembl:ENSG00000196236 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1183099963 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_214518,RMVar_hsa_circ_83622,RMVar_hsa_circ_269191,RMVar_hsa_circ_126281,RMVar_hsa_circ_214517,RMVar_hsa_circ_98365,RMVar_hsa_circ_214526,RMVar_hsa_circ_214527 5163 RMVar_ID_5163 Human_SNP_ID_704393398 A-to-I Human chr22 + 40930390 40930390 40930390 TGACCTCATAATCTGCCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCAC TGACCTCATAATCTGCCCACCTCAGCCTCCCAGAGTGCTGGGATTACAGGCGTGAGCCACTGCAC A G XPNPEP3 Ensembl:ENSG00000196236 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs138848856 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_34,Clinvar_Rec_35,Clinvar_Rec_36 RMVar_hsa_circ_214518,RMVar_hsa_circ_83622,RMVar_hsa_circ_269191,RMVar_hsa_circ_126281,RMVar_hsa_circ_214517,RMVar_hsa_circ_98365,RMVar_hsa_circ_214526,RMVar_hsa_circ_214527 5164 RMVar_ID_5164 Human_SNP_ID_704393627 A-to-I Human chr22 + 40931452 40931452 40931452 ATACTATAGTAAAGTTGGGTGCAGTGGATCACAGCTATAATCCCAGCACTTTGGGAGACCAAGGA ATACTATAGTAAAGTTGGGTGCAGTGGATCACCGCTATAATCCCAGCACTTTGGGAGACCAAGGA A C XPNPEP3 Ensembl:ENSG00000196236 Protein coding 3'UTR GSE47997;GSE38233;GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;cultured B-cells;cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,24183664,24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1228491483 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26498809 RMVar_hsa_circ_214518,RMVar_hsa_circ_83622,RMVar_hsa_circ_269191,RMVar_hsa_circ_126281,RMVar_hsa_circ_214517,RMVar_hsa_circ_98365,RMVar_hsa_circ_214526,RMVar_hsa_circ_214527 5165 RMVar_ID_5165 Human_SNP_ID_704393628 A-to-I Human chr22 + 40931456 40931453 40931456 TATAGTAAAGTTGGGTGCAGTGGATCACAGCTATAATCCCAGCACTTTGGGAGACCAAGGAGGGA TATAGTAAAGTTGGGTGCAGTGGATCACAG___TAATCCCAGCACTTTGGGAGACCAAGGAGGGA GCTA G XPNPEP3 Ensembl:ENSG00000196236 Protein coding 3'UTR GSE47997;GSE38233;GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;cultured B-cells;cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,24183664,24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1380931572 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_26498809 RMVar_hsa_circ_214518,RMVar_hsa_circ_83622,RMVar_hsa_circ_269191,RMVar_hsa_circ_126281,RMVar_hsa_circ_214517,RMVar_hsa_circ_98365,RMVar_hsa_circ_214526,RMVar_hsa_circ_214527 5166 RMVar_ID_5166 Human_SNP_ID_704393629 A-to-I Human chr22 + 40931458 40931458 40931458 TAGTAAAGTTGGGTGCAGTGGATCACAGCTATAATCCCAGCACTTTGGGAGACCAAGGAGGGATG TAGTAAAGTTGGGTGCAGTGGATCACAGCTATGATCCCAGCACTTTGGGAGACCAAGGAGGGATG A G XPNPEP3 Ensembl:ENSG00000196236 Protein coding 3'UTR GSE47997;GSE38233;GSE38233;GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;cultured B-cells;cultured B-cells;cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 23474544,24183664,24183664,24183664,31158229,31158229 RNA-Seq:(High) rs903330033 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26498809 RMVar_hsa_circ_214518,RMVar_hsa_circ_83622,RMVar_hsa_circ_269191,RMVar_hsa_circ_126281,RMVar_hsa_circ_214517,RMVar_hsa_circ_98365,RMVar_hsa_circ_214526,RMVar_hsa_circ_214527 5167 RMVar_ID_5167 Human_SNP_ID_704393664 A-to-I Human chr22 + 40931587 40931587 40931587 AAATTTAAAGTTAGCCAGGTGTGGTGGTTTGCACCTATAGTCCCAGCTACTCAGGAGGCTGAGGT AAATTTAAAGTTAGCCAGGTGTGGTGGTTTGCTCCTATAGTCCCAGCTACTCAGGAGGCTGAGGT A T XPNPEP3 Ensembl:ENSG00000196236 Protein coding 3'UTR GSE38233;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;Bronchiolar epithelium,BERP35T4 cell line - 24183664,31158229 RNA-Seq:(High) rs1425683614 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_214518,RMVar_hsa_circ_83622,RMVar_hsa_circ_269191,RMVar_hsa_circ_126281,RMVar_hsa_circ_214517,RMVar_hsa_circ_98365,RMVar_hsa_circ_214526,RMVar_hsa_circ_214527 5168 RMVar_ID_5168 Human_SNP_ID_704393666 A-to-I Human chr22 + 40931591 40931591 40931591 TTAAAGTTAGCCAGGTGTGGTGGTTTGCACCTATAGTCCCAGCTACTCAGGAGGCTGAGGTGGGA TTAAAGTTAGCCAGGTGTGGTGGTTTGCACCTGTAGTCCCAGCTACTCAGGAGGCTGAGGTGGGA A G XPNPEP3 Ensembl:ENSG00000196236 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,24183664,29129909,31158229,31158229 RNA-Seq:(High) rs1268817296 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_214518,RMVar_hsa_circ_83622,RMVar_hsa_circ_269191,RMVar_hsa_circ_126281,RMVar_hsa_circ_214517,RMVar_hsa_circ_98365,RMVar_hsa_circ_214526,RMVar_hsa_circ_214527 5169 RMVar_ID_5169 Human_SNP_ID_704393682 A-to-I Human chr22 + 40931696 40931696 40931696 TGATTGTGCCACTTCACCCTGGGCAACAGAGAAAGACCCTGTCTCAATAAAAAAGAAGAGAAAAA TGATTGTGCCACTTCACCCTGGGCAACAGAGAGAGACCCTGTCTCAATAAAAAAGAAGAGAAAAA A G XPNPEP3 Ensembl:ENSG00000196236 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs11557846 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2158256 RMVar_hsa_circ_214518,RMVar_hsa_circ_83622,RMVar_hsa_circ_269191,RMVar_hsa_circ_126281,RMVar_hsa_circ_214517,RMVar_hsa_circ_98365,RMVar_hsa_circ_214526,RMVar_hsa_circ_214527 5170 RMVar_ID_5170 Human_SNP_ID_704399978 A-to-I Human chr22 + 40955289 40955289 40955289 TTCCTTTTTTTTTTTTTTTGTTTTTTTCAGAGACGGGATCTCGCTTTGTTGCCCAGGCTGGTCTC TTCCTTTTTTTTTTTTTTTGTTTTTTTCAGAGTCGGGATCTCGCTTTGTTGCCCAGGCTGGTCTC A T RBX1 Ensembl:ENSG00000100387 Protein coding intron GSE38233;GSE107867 cultured B-cells;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 24183664,30559470 RNA-Seq:(High) rs1467378616 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7085640,Human_RBP_ID_14501644 RMVar_hsa_circ_214518,RMVar_hsa_circ_83622,RMVar_hsa_circ_126281,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 5171 RMVar_ID_5171 Human_SNP_ID_704399996 A-to-I Human chr22 + 40955360 40955360 40955360 GCTTCAAGTGATCCTCCCACTTTGGCCTTCCAAAATGTTGCGATTATAGGCGTGAGCCACTGTGG GCTTCAAGTGATCCTCCCACTTTGGCCTTCCAGAATGTTGCGATTATAGGCGTGAGCCACTGTGG A G RBX1 Ensembl:ENSG00000100387 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs989252842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14501652,Human_RBP_ID_25673498 RMVar_hsa_circ_214518,RMVar_hsa_circ_83622,RMVar_hsa_circ_126281,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 5172 RMVar_ID_5172 Human_SNP_ID_704400350 A-to-I Human chr22 + 40956780 40956780 40956780 CTCTTAGGCCAGGCGTGGTGGCTTACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGCAG CTCTTAGGCCAGGCGTGGTGGCTTACACCTGTGATCCCAGCACTTTGGGAGGCCAAGGCGGGCAG A G RBX1 Ensembl:ENSG00000100387 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1460176919 Functional Loss SNV dbSNP153 33..33 33 - - - 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 5173 RMVar_ID_5173 Human_SNP_ID_704400571 A-to-I Human chr22 + 40957547 40957547 40957547 GTGGTCCCAGCTACTTGGGAGGCTGAGGTGGGAAGATCCCTTGAGCCCGGGAGGCAGAGGTGACA GTGGTCCCAGCTACTTGGGAGGCTGAGGTGGGCAGATCCCTTGAGCCCGGGAGGCAGAGGTGACA A C RBX1 Ensembl:ENSG00000100387 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1321299195 Functional Loss SNV dbSNP153 33..33 33 - - - 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 5174 RMVar_ID_5174 Human_SNP_ID_704400655 A-to-I Human chr22 + 40957911 40957911 40957911 CAGTGGCACGATCTCGGCTTACTGCAGTCTCCACCTTCTGGGTTCAAACAATTCTCCTGCCTCAG CAGTGGCACGATCTCGGCTTACTGCAGTCTCCGCCTTCTGGGTTCAAACAATTCTCCTGCCTCAG A G RBX1 Ensembl:ENSG00000100387 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1338527352 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14501739 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 5175 RMVar_ID_5175 Human_SNP_ID_704400677 A-to-I Human chr22 + 40958026 40958026 40958026 TTTTGTATTTTTAGTAGAAATGGGGTTTCACTATGTTGGCCAGGCTGGTCTCGAGCTCCTGACCT TTTTGTATTTTTAGTAGAAATGGGGTTTCACTGTGTTGGCCAGGCTGGTCTCGAGCTCCTGACCT A G RBX1 Ensembl:ENSG00000100387 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1283413227 Functional Loss SNV dbSNP153 33..33 33 - - - 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 5176 RMVar_ID_5176 Human_SNP_ID_704400690 A-to-I Human chr22 + 40958083 40958083 40958083 CCTGACCTCATGATCACCCATCTCGGCCCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCAT CCTGACCTCATGATCACCCATCTCGGCCCCCAGAGTGCTGGGATTACAGGTGTGAGCCACCGCAT A G RBX1 Ensembl:ENSG00000100387 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1163361209 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14501741 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 5177 RMVar_ID_5177 Human_SNP_ID_704400888 A-to-I Human chr22 + 40958943 40958943 40958943 TCAAGCTATTCTCCTGCCTCAGCCTCCTGAGCAGCTGAGACTGCAGGTATGCACCAGCATGCCCA TCAAGCTATTCTCCTGCCTCAGCCTCCTGAGCGGCTGAGACTGCAGGTATGCACCAGCATGCCCA A G RBX1 Ensembl:ENSG00000100387 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1358636373 Functional Loss SNV dbSNP153 33..33 33 - - - 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 5178 RMVar_ID_5178 Human_SNP_ID_704400898 A-to-I Human chr22 + 40958997 40958997 40958997 CAGCATGCCCAGCTAATTTTTGTATTTTTAGTAGAAACAGGGTTTCACCATGTTGGCCAGTCTGG CAGCATGCCCAGCTAATTTTTGTATTTTTAGTGGAAACAGGGTTTCACCATGTTGGCCAGTCTGG A G RBX1 Ensembl:ENSG00000100387 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs752944784 Functional Loss SNV dbSNP153 33..33 33 - - - 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 5179 RMVar_ID_5179 Human_SNP_ID_704401072 A-to-I Human chr22 + 40959668 40959668 40959668 CCCCATCTCTACTAAAAATACAAAAAATAGCCAGGCATGGTGGCGCATGCCTGTAGTCCCAGCTA CCCCATCTCTACTAAAAATACAAAAAATAGCCCGGCATGGTGGCGCATGCCTGTAGTCCCAGCTA A C RBX1 Ensembl:ENSG00000100387 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs536356637 Functional Loss SNV dbSNP153 33..33 33 - - - 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 5180 RMVar_ID_5180 Human_SNP_ID_704401127 A-to-I Human chr22 + 40959861 40959861 40959861 AATCTTGGTCGGATGCAGTGGCTCACGCCTGTAATCTCAGCACCATGGGAGGCCGAGGCAGGCAG AATCTTGGTCGGATGCAGTGGCTCACGCCTGTGATCTCAGCACCATGGGAGGCCGAGGCAGGCAG A G RBX1 Ensembl:ENSG00000100387 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1242271300 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14501812 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 5181 RMVar_ID_5181 Human_SNP_ID_704401382 A-to-I Human chr22 + 40960953 40960952 40960954 CCCGGTTAATTGTTTGTATTTTTAGAAGAGACAGAGTTTCGCCATGTTGGCCAGGCTGGTCTCGA CCCGGTTAATTGTTTGTATTTTTAGAAGAGAC__AGTTTCGCCATGTTGGCCAGGCTGGTCTCGA CAG C RBX1 Ensembl:ENSG00000100387 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1428193783 Functional Loss DEL dbSNP153 33..34 33 - - - 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 5182 RMVar_ID_5182 Human_SNP_ID_704401707 A-to-I Human chr22 + 40961968 40961967 40961969 CACCATGCCTGGCTAATTTTTGCCTTCTTAGTAGAGAGGGGGTTTTGCCATGTTTGCCAGGCTGG CACCATGCCTGGCTAATTTTTGCCTTCTTAGT__AGAGGGGGTTTTGCCATGTTTGCCAGGCTGG TAG T RBX1 Ensembl:ENSG00000100387 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1322260042 Functional Loss DEL dbSNP153 33..34 33 - - - 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 5183 RMVar_ID_5183 Human_SNP_ID_704401764 A-to-I Human chr22 + 40962123 40962122 40962124 GTTTGTTTGTTTGTTTGTTTGTTTTTTGAGACAGAGTCTTGCTCTTTTGCCCAGGCTGGAGTACA GTTTGTTTGTTTGTTTGTTTGTTTTTTGAGAC__AGTCTTGCTCTTTTGCCCAGGCTGGAGTACA CAG C RBX1 Ensembl:ENSG00000100387 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1397705973 Functional Loss DEL dbSNP153 33..34 33 - - - 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 5184 RMVar_ID_5184 Human_SNP_ID_704401786 A-to-I Human chr22 + 40962227 40962227 40962227 GGGTTCAAGCAATTCTCCTACCTCAGCCTCCCAAGTAACTGGGATTGCAGACATGTACCACCATG GGGTTCAAGCAATTCTCCTACCTCAGCCTCCCTAGTAACTGGGATTGCAGACATGTACCACCATG A T RBX1 Ensembl:ENSG00000100387 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs962738864 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14501882 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 5185 RMVar_ID_5185 Human_SNP_ID_704401788 A-to-I Human chr22 + 40962231 40962231 40962231 TCAAGCAATTCTCCTACCTCAGCCTCCCAAGTAACTGGGATTGCAGACATGTACCACCATGCACC TCAAGCAATTCTCCTACCTCAGCCTCCCAAGTGACTGGGATTGCAGACATGTACCACCATGCACC A G RBX1 Ensembl:ENSG00000100387 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1241855609 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14501882 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 5186 RMVar_ID_5186 Human_SNP_ID_704402002 A-to-I Human chr22 + 40962957 40962957 40962957 TGACCTCATGATGTGCCTGCCTCGGCCTCCCAAAGTGCTGAGATTACAGGAGTGAGCCATCGCGC TGACCTCATGATGTGCCTGCCTCGGCCTCCCAGAGTGCTGAGATTACAGGAGTGAGCCATCGCGC A G RBX1 Ensembl:ENSG00000100387 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs979085693 Functional Loss SNV dbSNP153 33..33 33 - - - 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 5187 RMVar_ID_5187 Human_SNP_ID_704402025 A-to-I Human chr22 + 40963042 40963042 40963042 TTTTCATATTTTTAGTAGAGACAGGTTTCACCATGTTGGGTGGGCTAGTCTTGAACTCCTGACCT TTTTCATATTTTTAGTAGAGACAGGTTTCACCGTGTTGGGTGGGCTAGTCTTGAACTCCTGACCT A G RBX1 Ensembl:ENSG00000100387 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1439050918 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14501902 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 5188 RMVar_ID_5188 Human_SNP_ID_704402119 A-to-I Human chr22 + 40963515 40963515 40963515 AAATTAGCCAGGCATGGTGGTGTGCGCCTGTTAATTCCAGCTACTTGGGAGTCTGAGACACGAGA AAATTAGCCAGGCATGGTGGTGTGCGCCTGTTGATTCCAGCTACTTGGGAGTCTGAGACACGAGA A G RBX1 Ensembl:ENSG00000100387 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs995708003 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14501926 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 5189 RMVar_ID_5189 Human_SNP_ID_704402156 A-to-I Human chr22 + 40963678 40963678 40963678 AAAACTCAGTCTAGGCAACATGGTGAAACTCCATCTCTACAAAAAATACAAACAATTAGCTGGTG AAAACTCAGTCTAGGCAACATGGTGAAACTCCGTCTCTACAAAAAATACAAACAATTAGCTGGTG A G RBX1 Ensembl:ENSG00000100387 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs889081450 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20767774 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 5190 RMVar_ID_5190 Human_SNP_ID_704402493 A-to-I Human chr22 + 40965049 40965049 40965049 TAAATAGGCCGGACGCGGTGGCTCACGCCTGTAATCCCAGCACTCTGGGAGGCCGAGGCGGGTGC TAAATAGGCCGGACGCGGTGGCTCACGCCTGTGATCCCAGCACTCTGGGAGGCCGAGGCGGGTGC A G RBX1 Ensembl:ENSG00000100387 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1172256877 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83622,RMVar_hsa_circ_214517,RMVar_hsa_circ_270699,RMVar_hsa_circ_214532,RMVar_hsa_circ_360751,RMVar_hsa_circ_214535 5191 RMVar_ID_5191 Human_SNP_ID_704402621 A-to-I Human chr22 + 40965472 40965472 40965472 TGTTTTTTGTTTTTTTTTTGAGACGGAGTCTCACTATGTGGCCCAGGCTGGAGCGCAGTGACGCA TGTTTTTTGTTTTTTTTTTGAGACGGAGTCTCCCTATGTGGCCCAGGCTGGAGCGCAGTGACGCA A C RBX1 Ensembl:ENSG00000100387 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1301444414 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83622,RMVar_hsa_circ_214517,RMVar_hsa_circ_270699,RMVar_hsa_circ_214532,RMVar_hsa_circ_360751,RMVar_hsa_circ_214535 5192 RMVar_ID_5192 Human_SNP_ID_704402655 A-to-I Human chr22 + 40965624 40965624 40965624 CACCACACCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCGCCATGTTGGCCAGGCTGG CACCACACCCAGCTAATTTTTGTATTTTTAGTGGAGATGGGGTTTCGCCATGTTGGCCAGGCTGG A G RBX1 Ensembl:ENSG00000100387 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1001567209 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83622,RMVar_hsa_circ_214517,RMVar_hsa_circ_270699,RMVar_hsa_circ_214532,RMVar_hsa_circ_360751,RMVar_hsa_circ_214535 5193 RMVar_ID_5193 Human_SNP_ID_704428149 A-to-I Human chr22 - 41064276 41064276 41064276 ACCCCAATGCAGACCAGCCGCCACAGCAGGGCATTGCCTTCGAACAGACGCCGTGGGTCCTTCTG ACCCCAATGCAGACCAGCCGCCACAGCAGGGCGTTGCCTTCGAACAGACGCCGTGGGTCCTTCTG T C L13705-009,L13304-001 RNACentral:URS00001E2917,RNACentral:URS000044B5AA misc_RNA,scRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879050166 Functional Loss SNV dbSNP153 33..33 33 - - - 5194 RMVar_ID_5194 Human_SNP_ID_704428150 A-to-I Human chr22 - 41064276 41064276 41064276 ACCCCAATGCAGACCAGCCGCCACAGCAGGGCATTGCCTTCGAACAGACGCCGTGGGTCCTTCTG ACCCCAATGCAGACCAGCCGCCACAGCAGGGCCTTGCCTTCGAACAGACGCCGTGGGTCCTTCTG T G L13705-009,L13304-001 RNACentral:URS00001E2917,RNACentral:URS000044B5AA misc_RNA,scRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879050166 Functional Loss SNV dbSNP153 33..33 33 - - - 5195 RMVar_ID_5195 Human_SNP_ID_704428154 A-to-I Human chr22 - 41064286 41064286 41064286 CTCATCCAGCACCCCAATGCAGACCAGCCGCCACAGCAGGGCATTGCCTTCGAACAGACGCCGTG CTCATCCAGCACCCCAATGCAGACCAGCCGCCGCAGCAGGGCATTGCCTTCGAACAGACGCCGTG T C L13705-009,L13304-001 RNACentral:URS00001E2917,RNACentral:URS000044B5AA misc_RNA,scRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879168972 Functional Loss SNV dbSNP153 33..33 33 - - - 5196 RMVar_ID_5196 Human_SNP_ID_704428156 A-to-I Human chr22 - 41064298 41064298 41064298 CTTCATCTTGCCCTCATCCAGCACCCCAATGCAGACCAGCCGCCACAGCAGGGCATTGCCTTCGA CTTCATCTTGCCCTCATCCAGCACCCCAATGCGGACCAGCCGCCACAGCAGGGCATTGCCTTCGA T C L13705-009,L13304-001 RNACentral:URS00001E2917,RNACentral:URS000044B5AA misc_RNA,scRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879101686 Functional Loss SNV dbSNP153 33..33 33 - - - 5197 RMVar_ID_5197 Human_SNP_ID_704438270 A-to-I Human chr22 + 41099280 41099280 41099280 GAGACAGGGAGTCCTGACCTCGTGATCCACCCACCTCGGCCTCCCAAAATGTTGGGATTACAGGC GAGACAGGGAGTCCTGACCTCGTGATCCACCCGCCTCGGCCTCCCAAAATGTTGGGATTACAGGC A G EP300 Ensembl:ENSG00000100393 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs899262696 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_214536,RMVar_hsa_circ_96967,RMVar_hsa_circ_112894,RMVar_hsa_circ_214537 5198 RMVar_ID_5198 Human_SNP_ID_704438271 A-to-I Human chr22 + 41099280 41099280 41099280 GAGACAGGGAGTCCTGACCTCGTGATCCACCCACCTCGGCCTCCCAAAATGTTGGGATTACAGGC GAGACAGGGAGTCCTGACCTCGTGATCCACCCTCCTCGGCCTCCCAAAATGTTGGGATTACAGGC A T EP300 Ensembl:ENSG00000100393 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs899262696 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_214536,RMVar_hsa_circ_96967,RMVar_hsa_circ_112894,RMVar_hsa_circ_214537 5199 RMVar_ID_5199 Human_SNP_ID_704444008 A-to-I Human chr22 + 41116877 41116877 41116877 CAGCTCAGGAGTGTAAGACCAGCCAGGTCAACATGGCAAGCTCCGCCTCTACTAAAAATACAAAA CAGCTCAGGAGTGTAAGACCAGCCAGGTCAACGTGGCAAGCTCCGCCTCTACTAAAAATACAAAA A G EP300 Ensembl:ENSG00000100393 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs951135125 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_214536,RMVar_hsa_circ_96967,RMVar_hsa_circ_112894,RMVar_hsa_circ_214537 5200 RMVar_ID_5200 Human_SNP_ID_704444028 A-to-I Human chr22 + 41116939 41116939 41116939 AAATTTAGCTCGGTGTGGTGGTGCGCACTTGTAGTCACAGCTACTTGGGAGGCTGAGATGGTAGA AAATTTAGCTCGGTGTGGTGGTGCGCACTTGTCGTCACAGCTACTTGGGAGGCTGAGATGGTAGA A C EP300 Ensembl:ENSG00000100393 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1252330116 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_214536,RMVar_hsa_circ_96967,RMVar_hsa_circ_112894,RMVar_hsa_circ_214537 5201 RMVar_ID_5201 Human_SNP_ID_704445349 A-to-I Human chr22 + 41120844 41120832 41120845 AGGCTTACGCGATCCTCCTACCTCAGACTCCTAAGTAGCTAGTACTACAAGGACTGTCATGCCCT AGGCTTACGCGATCCTCCTAC_____________GTAGCTAGTACTACAAGGACTGTCATGCCCT CCTCAGACTCCTAA C EP300 Ensembl:ENSG00000100393 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs908067198 Functional Loss DEL dbSNP153 22..34 33 - - - Human_RBP_ID_14503150 RMVar_hsa_circ_61612,RMVar_hsa_circ_214536,RMVar_hsa_circ_96967,RMVar_hsa_circ_112894,RMVar_hsa_circ_214537,RMVar_hsa_circ_303989,RMVar_hsa_circ_316674,RMVar_hsa_circ_342320,RMVar_hsa_circ_350989,RMVar_hsa_circ_360687,RMVar_hsa_circ_318286,RMVar_hsa_circ_308943,RMVar_hsa_circ_282404,RMVar_hsa_circ_67948,RMVar_hsa_circ_214539,RMVar_hsa_circ_214540,RMVar_hsa_circ_214538 5202 RMVar_ID_5202 Human_SNP_ID_704445351 A-to-I Human chr22 + 41120844 41120844 41120844 AGGCTTACGCGATCCTCCTACCTCAGACTCCTAAGTAGCTAGTACTACAAGGACTGTCATGCCCT AGGCTTACGCGATCCTCCTACCTCAGACTCCTGAGTAGCTAGTACTACAAGGACTGTCATGCCCT A G EP300 Ensembl:ENSG00000100393 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1242068674 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14503150 RMVar_hsa_circ_61612,RMVar_hsa_circ_214536,RMVar_hsa_circ_96967,RMVar_hsa_circ_112894,RMVar_hsa_circ_214537,RMVar_hsa_circ_303989,RMVar_hsa_circ_316674,RMVar_hsa_circ_342320,RMVar_hsa_circ_350989,RMVar_hsa_circ_360687,RMVar_hsa_circ_318286,RMVar_hsa_circ_308943,RMVar_hsa_circ_282404,RMVar_hsa_circ_67948,RMVar_hsa_circ_214539,RMVar_hsa_circ_214540,RMVar_hsa_circ_214538 5203 RMVar_ID_5203 Human_SNP_ID_704450391 A-to-I Human chr22 + 41136540 41136540 41136540 AAAGTTAACGGGGCATGGTGGCGTGCACCTGTAGTCCCAGCTACTGATGAGGCTGAGGTGGGAGG AAAGTTAACGGGGCATGGTGGCGTGCACCTGTGGTCCCAGCTACTGATGAGGCTGAGGTGGGAGG A G EP300 Ensembl:ENSG00000100393 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1302261496 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25673894 RMVar_hsa_circ_214543,RMVar_hsa_circ_61612,RMVar_hsa_circ_214536,RMVar_hsa_circ_96967,RMVar_hsa_circ_112894,RMVar_hsa_circ_214537,RMVar_hsa_circ_303989,RMVar_hsa_circ_350989,RMVar_hsa_circ_360687,RMVar_hsa_circ_67948,RMVar_hsa_circ_214539,RMVar_hsa_circ_214538,RMVar_hsa_circ_290513,RMVar_hsa_circ_343214,RMVar_hsa_circ_357085,RMVar_hsa_circ_357569,RMVar_hsa_circ_289102,RMVar_hsa_circ_289966,RMVar_hsa_circ_125932,RMVar_hsa_circ_120724,RMVar_hsa_circ_80226,RMVar_hsa_circ_89813,RMVar_hsa_circ_214547,RMVar_hsa_circ_214549,RMVar_hsa_circ_214550,RMVar_hsa_circ_214548,RMVar_hsa_circ_214545,RMVar_hsa_circ_214546,RMVar_hsa_circ_214544,RMVar_hsa_circ_100237,RMVar_hsa_circ_214557,RMVar_hsa_circ_102183,RMVar_hsa_circ_103802,RMVar_hsa_circ_101874,RMVar_hsa_circ_214558,RMVar_hsa_circ_344108,RMVar_hsa_circ_214556,RMVar_hsa_circ_214560,RMVar_hsa_circ_74330,RMVar_hsa_circ_337665,RMVar_hsa_circ_214559,RMVar_hsa_circ_309269,RMVar_hsa_circ_122834,RMVar_hsa_circ_267084,RMVar_hsa_circ_114332,RMVar_hsa_circ_67686,RMVar_hsa_circ_281247,RMVar_hsa_circ_214563,RMVar_hsa_circ_214565,RMVar_hsa_circ_214566,RMVar_hsa_circ_214564,RMVar_hsa_circ_321588,RMVar_hsa_circ_275617,RMVar_hsa_circ_278510,RMVar_hsa_circ_265093,RMVar_hsa_circ_214567,RMVar_hsa_circ_214568,RMVar_hsa_circ_214569 5204 RMVar_ID_5204 Human_SNP_ID_704452057 A-to-I Human chr22 + 41141866 41141866 41141866 GCCTGTCTAATTTTTGTATTTTTCGTAGAGACAGGGTTTTGCCATGTTGGCCTAGCTGATCTCAA GCCTGTCTAATTTTTGTATTTTTCGTAGAGACGGGGTTTTGCCATGTTGGCCTAGCTGATCTCAA A G EP300 Ensembl:ENSG00000100393 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs114980245 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_37 RMVar_hsa_circ_214543,RMVar_hsa_circ_61612,RMVar_hsa_circ_96967,RMVar_hsa_circ_214537,RMVar_hsa_circ_360687,RMVar_hsa_circ_357085,RMVar_hsa_circ_357569,RMVar_hsa_circ_289966,RMVar_hsa_circ_125932,RMVar_hsa_circ_120724,RMVar_hsa_circ_80226,RMVar_hsa_circ_89813,RMVar_hsa_circ_214547,RMVar_hsa_circ_214548,RMVar_hsa_circ_214545,RMVar_hsa_circ_214546,RMVar_hsa_circ_214544,RMVar_hsa_circ_100237,RMVar_hsa_circ_214557,RMVar_hsa_circ_102183,RMVar_hsa_circ_101874,RMVar_hsa_circ_214558,RMVar_hsa_circ_74330,RMVar_hsa_circ_214559,RMVar_hsa_circ_122834,RMVar_hsa_circ_267084,RMVar_hsa_circ_114332,RMVar_hsa_circ_67686,RMVar_hsa_circ_281247,RMVar_hsa_circ_214565,RMVar_hsa_circ_214566,RMVar_hsa_circ_265093,RMVar_hsa_circ_214569,RMVar_hsa_circ_320234,RMVar_hsa_circ_214573,RMVar_hsa_circ_214574,RMVar_hsa_circ_357329,RMVar_hsa_circ_365393,RMVar_hsa_circ_360639,RMVar_hsa_circ_124497 5205 RMVar_ID_5205 Human_SNP_ID_704452077 A-to-I Human chr22 + 41141945 41141945 41141945 ATGATCCGCCCACCTTGGCATCCCAAAGTACTAGGATTACAGGCATGAGCCACCACTCCCTGCCT ATGATCCGCCCACCTTGGCATCCCAAAGTACTGGGATTACAGGCATGAGCCACCACTCCCTGCCT A G EP300 Ensembl:ENSG00000100393 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1173351610 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_214543,RMVar_hsa_circ_61612,RMVar_hsa_circ_96967,RMVar_hsa_circ_214537,RMVar_hsa_circ_360687,RMVar_hsa_circ_357085,RMVar_hsa_circ_357569,RMVar_hsa_circ_289966,RMVar_hsa_circ_125932,RMVar_hsa_circ_120724,RMVar_hsa_circ_80226,RMVar_hsa_circ_89813,RMVar_hsa_circ_214547,RMVar_hsa_circ_214548,RMVar_hsa_circ_214545,RMVar_hsa_circ_214546,RMVar_hsa_circ_214544,RMVar_hsa_circ_100237,RMVar_hsa_circ_214557,RMVar_hsa_circ_102183,RMVar_hsa_circ_101874,RMVar_hsa_circ_214558,RMVar_hsa_circ_74330,RMVar_hsa_circ_214559,RMVar_hsa_circ_122834,RMVar_hsa_circ_267084,RMVar_hsa_circ_114332,RMVar_hsa_circ_67686,RMVar_hsa_circ_281247,RMVar_hsa_circ_214565,RMVar_hsa_circ_214566,RMVar_hsa_circ_265093,RMVar_hsa_circ_214569,RMVar_hsa_circ_320234,RMVar_hsa_circ_214573,RMVar_hsa_circ_214574,RMVar_hsa_circ_357329,RMVar_hsa_circ_365393,RMVar_hsa_circ_360639,RMVar_hsa_circ_124497 5206 RMVar_ID_5206 Human_SNP_ID_704452274 A-to-I Human chr22 + 41142713 41142713 41142713 GGAGACCATCCTGGCTAACACGGTGAAACCCCATCTCTACTAAAAATACAAAACAATTAGCCGGG GGAGACCATCCTGGCTAACACGGTGAAACCCCGTCTCTACTAAAAATACAAAACAATTAGCCGGG A G EP300 Ensembl:ENSG00000100393 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1172933253 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_214543,RMVar_hsa_circ_61612,RMVar_hsa_circ_96967,RMVar_hsa_circ_214537,RMVar_hsa_circ_360687,RMVar_hsa_circ_357085,RMVar_hsa_circ_357569,RMVar_hsa_circ_289966,RMVar_hsa_circ_125932,RMVar_hsa_circ_120724,RMVar_hsa_circ_80226,RMVar_hsa_circ_89813,RMVar_hsa_circ_214547,RMVar_hsa_circ_214548,RMVar_hsa_circ_214545,RMVar_hsa_circ_214546,RMVar_hsa_circ_214544,RMVar_hsa_circ_100237,RMVar_hsa_circ_214557,RMVar_hsa_circ_102183,RMVar_hsa_circ_101874,RMVar_hsa_circ_214558,RMVar_hsa_circ_74330,RMVar_hsa_circ_214559,RMVar_hsa_circ_122834,RMVar_hsa_circ_267084,RMVar_hsa_circ_114332,RMVar_hsa_circ_67686,RMVar_hsa_circ_281247,RMVar_hsa_circ_214565,RMVar_hsa_circ_214566,RMVar_hsa_circ_265093,RMVar_hsa_circ_214569,RMVar_hsa_circ_320234,RMVar_hsa_circ_214573,RMVar_hsa_circ_214574,RMVar_hsa_circ_357329,RMVar_hsa_circ_365393,RMVar_hsa_circ_360639,RMVar_hsa_circ_124497 5207 RMVar_ID_5207 Human_SNP_ID_704452461 A-to-I Human chr22 + 41143313 41143313 41143313 GTCTCTATAAAAAATACAAAAATTAGCCAGGCATGGAGGTGTGTGCCTGTAGTCCCAGCTACTCA GTCTCTATAAAAAATACAAAAATTAGCCAGGCCTGGAGGTGTGTGCCTGTAGTCCCAGCTACTCA A C EP300 Ensembl:ENSG00000100393 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1254349309 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_214543,RMVar_hsa_circ_61612,RMVar_hsa_circ_96967,RMVar_hsa_circ_214537,RMVar_hsa_circ_360687,RMVar_hsa_circ_357085,RMVar_hsa_circ_357569,RMVar_hsa_circ_289966,RMVar_hsa_circ_125932,RMVar_hsa_circ_120724,RMVar_hsa_circ_80226,RMVar_hsa_circ_89813,RMVar_hsa_circ_214547,RMVar_hsa_circ_214548,RMVar_hsa_circ_214545,RMVar_hsa_circ_214546,RMVar_hsa_circ_214544,RMVar_hsa_circ_100237,RMVar_hsa_circ_214557,RMVar_hsa_circ_102183,RMVar_hsa_circ_101874,RMVar_hsa_circ_214558,RMVar_hsa_circ_74330,RMVar_hsa_circ_214559,RMVar_hsa_circ_122834,RMVar_hsa_circ_267084,RMVar_hsa_circ_114332,RMVar_hsa_circ_67686,RMVar_hsa_circ_281247,RMVar_hsa_circ_214565,RMVar_hsa_circ_214566,RMVar_hsa_circ_265093,RMVar_hsa_circ_214569,RMVar_hsa_circ_320234,RMVar_hsa_circ_214573,RMVar_hsa_circ_214574,RMVar_hsa_circ_357329,RMVar_hsa_circ_365393,RMVar_hsa_circ_360639,RMVar_hsa_circ_124497 5208 RMVar_ID_5208 Human_SNP_ID_704452580 A-to-I Human chr22 + 41143669 41143669 41143669 ACCATCTAAGCTCACTGCAACCTCTGCCTCCCAGATTCAGTTGATTCTTGTACCTCAGCATCCCC ACCATCTAAGCTCACTGCAACCTCTGCCTCCCGGATTCAGTTGATTCTTGTACCTCAGCATCCCC A G EP300 Ensembl:ENSG00000100393 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1224270483 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14503503 RMVar_hsa_circ_214543,RMVar_hsa_circ_61612,RMVar_hsa_circ_96967,RMVar_hsa_circ_214537,RMVar_hsa_circ_360687,RMVar_hsa_circ_357085,RMVar_hsa_circ_357569,RMVar_hsa_circ_289966,RMVar_hsa_circ_125932,RMVar_hsa_circ_120724,RMVar_hsa_circ_80226,RMVar_hsa_circ_89813,RMVar_hsa_circ_214547,RMVar_hsa_circ_214548,RMVar_hsa_circ_214545,RMVar_hsa_circ_214546,RMVar_hsa_circ_214544,RMVar_hsa_circ_100237,RMVar_hsa_circ_214557,RMVar_hsa_circ_102183,RMVar_hsa_circ_101874,RMVar_hsa_circ_214558,RMVar_hsa_circ_74330,RMVar_hsa_circ_214559,RMVar_hsa_circ_122834,RMVar_hsa_circ_267084,RMVar_hsa_circ_114332,RMVar_hsa_circ_67686,RMVar_hsa_circ_281247,RMVar_hsa_circ_214565,RMVar_hsa_circ_214566,RMVar_hsa_circ_265093,RMVar_hsa_circ_214569,RMVar_hsa_circ_320234,RMVar_hsa_circ_214573,RMVar_hsa_circ_214574,RMVar_hsa_circ_357329,RMVar_hsa_circ_365393,RMVar_hsa_circ_360639,RMVar_hsa_circ_124497 5209 RMVar_ID_5209 Human_SNP_ID_704452599 A-to-I Human chr22 + 41143751 41143751 41143751 GCATGCATCACCACACCTAACTAATGTTTTGTATTTTCAGTAGAGACAGGGTTTCACACCATGTT GCATGCATCACCACACCTAACTAATGTTTTGTGTTTTCAGTAGAGACAGGGTTTCACACCATGTT A G EP300 Ensembl:ENSG00000100393 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1265633725 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14503505 RMVar_hsa_circ_214543,RMVar_hsa_circ_61612,RMVar_hsa_circ_96967,RMVar_hsa_circ_214537,RMVar_hsa_circ_360687,RMVar_hsa_circ_357085,RMVar_hsa_circ_357569,RMVar_hsa_circ_289966,RMVar_hsa_circ_125932,RMVar_hsa_circ_120724,RMVar_hsa_circ_80226,RMVar_hsa_circ_89813,RMVar_hsa_circ_214547,RMVar_hsa_circ_214548,RMVar_hsa_circ_214545,RMVar_hsa_circ_214546,RMVar_hsa_circ_214544,RMVar_hsa_circ_100237,RMVar_hsa_circ_214557,RMVar_hsa_circ_102183,RMVar_hsa_circ_101874,RMVar_hsa_circ_214558,RMVar_hsa_circ_74330,RMVar_hsa_circ_214559,RMVar_hsa_circ_122834,RMVar_hsa_circ_267084,RMVar_hsa_circ_114332,RMVar_hsa_circ_67686,RMVar_hsa_circ_281247,RMVar_hsa_circ_214565,RMVar_hsa_circ_214566,RMVar_hsa_circ_265093,RMVar_hsa_circ_214569,RMVar_hsa_circ_320234,RMVar_hsa_circ_214573,RMVar_hsa_circ_214574,RMVar_hsa_circ_357329,RMVar_hsa_circ_365393,RMVar_hsa_circ_360639,RMVar_hsa_circ_124497 5210 RMVar_ID_5210 Human_SNP_ID_704455631 A-to-I Human chr22 + 41152923 41152923 41152923 GGGACTGCATGCGCATGCCACCATGCCCGTCTAATTTTTGTATTTTTAGTAGAGACAGGATTTCA GGGACTGCATGCGCATGCCACCATGCCCGTCTGATTTTTGTATTTTTAGTAGAGACAGGATTTCA A G EP300 Ensembl:ENSG00000100393 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1420292660 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_214543,RMVar_hsa_circ_61612,RMVar_hsa_circ_357085,RMVar_hsa_circ_357569,RMVar_hsa_circ_102183,RMVar_hsa_circ_214558,RMVar_hsa_circ_267084,RMVar_hsa_circ_114332,RMVar_hsa_circ_214566,RMVar_hsa_circ_265093,RMVar_hsa_circ_357329,RMVar_hsa_circ_365393,RMVar_hsa_circ_360639,RMVar_hsa_circ_362344,RMVar_hsa_circ_346954,RMVar_hsa_circ_96540,RMVar_hsa_circ_33074,RMVar_hsa_circ_75156,RMVar_hsa_circ_214579,RMVar_hsa_circ_317494,RMVar_hsa_circ_33472,RMVar_hsa_circ_214580,RMVar_hsa_circ_25792 5211 RMVar_ID_5211 Human_SNP_ID_704455830 A-to-I Human chr22 + 41153585 41153585 41153585 CAGCCTGGCCAATATGGTGAAACTCTGTCTCTACTAAAAGTACAAAAGTTAGCCGGGTGTGGTGG CAGCCTGGCCAATATGGTGAAACTCTGTCTCTGCTAAAAGTACAAAAGTTAGCCGGGTGTGGTGG A G EP300 Ensembl:ENSG00000100393 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1485828755 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_214543,RMVar_hsa_circ_61612,RMVar_hsa_circ_357085,RMVar_hsa_circ_357569,RMVar_hsa_circ_102183,RMVar_hsa_circ_214558,RMVar_hsa_circ_267084,RMVar_hsa_circ_114332,RMVar_hsa_circ_214566,RMVar_hsa_circ_265093,RMVar_hsa_circ_357329,RMVar_hsa_circ_365393,RMVar_hsa_circ_360639,RMVar_hsa_circ_362344,RMVar_hsa_circ_346954,RMVar_hsa_circ_96540,RMVar_hsa_circ_33074,RMVar_hsa_circ_75156,RMVar_hsa_circ_214579,RMVar_hsa_circ_317494,RMVar_hsa_circ_33472,RMVar_hsa_circ_214580,RMVar_hsa_circ_25792 5212 RMVar_ID_5212 Human_SNP_ID_704455847 A-to-I Human chr22 + 41153656 41153656 41153656 CCCGTAGTCCCATCTACTTGGGAGGCTGAGGCAGAAGAATCACTTGAACCCGGGAGATGGAAGGA CCCGTAGTCCCATCTACTTGGGAGGCTGAGGCGGAAGAATCACTTGAACCCGGGAGATGGAAGGA A G EP300 Ensembl:ENSG00000100393 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs774099167 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14503606 RMVar_hsa_circ_214543,RMVar_hsa_circ_61612,RMVar_hsa_circ_357085,RMVar_hsa_circ_357569,RMVar_hsa_circ_102183,RMVar_hsa_circ_214558,RMVar_hsa_circ_267084,RMVar_hsa_circ_114332,RMVar_hsa_circ_214566,RMVar_hsa_circ_265093,RMVar_hsa_circ_357329,RMVar_hsa_circ_365393,RMVar_hsa_circ_360639,RMVar_hsa_circ_362344,RMVar_hsa_circ_346954,RMVar_hsa_circ_96540,RMVar_hsa_circ_33074,RMVar_hsa_circ_75156,RMVar_hsa_circ_214579,RMVar_hsa_circ_317494,RMVar_hsa_circ_33472,RMVar_hsa_circ_214580,RMVar_hsa_circ_25792 5213 RMVar_ID_5213 Human_SNP_ID_704456134 A-to-I Human chr22 + 41154559 41154559 41154559 GCCACCATGTCCGACTAATTTTTTATATTTTTAGTAGAGACGAGGTTTCACCATGTTGGCCAGGC GCCACCATGTCCGACTAATTTTTTATATTTTTCGTAGAGACGAGGTTTCACCATGTTGGCCAGGC A C EP300 Ensembl:ENSG00000100393 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs935184570 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25674008 RMVar_hsa_circ_214543,RMVar_hsa_circ_61612,RMVar_hsa_circ_357085,RMVar_hsa_circ_357569,RMVar_hsa_circ_102183,RMVar_hsa_circ_214558,RMVar_hsa_circ_267084,RMVar_hsa_circ_114332,RMVar_hsa_circ_214566,RMVar_hsa_circ_265093,RMVar_hsa_circ_357329,RMVar_hsa_circ_365393,RMVar_hsa_circ_360639,RMVar_hsa_circ_362344,RMVar_hsa_circ_346954,RMVar_hsa_circ_96540,RMVar_hsa_circ_33074,RMVar_hsa_circ_75156,RMVar_hsa_circ_214579,RMVar_hsa_circ_317494,RMVar_hsa_circ_33472,RMVar_hsa_circ_214580,RMVar_hsa_circ_25792 5214 RMVar_ID_5214 Human_SNP_ID_704456604 A-to-I Human chr22 + 41156159 41156159 41156159 TCTCAGCCTCCCGAGTAGCTGGGATTACAGGCATGTGCCACCATGCCCGGCTAATTTTGTATTTT TCTCAGCCTCCCGAGTAGCTGGGATTACAGGCGTGTGCCACCATGCCCGGCTAATTTTGTATTTT A G EP300 Ensembl:ENSG00000100393 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1387393542 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_214543,RMVar_hsa_circ_61612,RMVar_hsa_circ_357085,RMVar_hsa_circ_357569,RMVar_hsa_circ_102183,RMVar_hsa_circ_214558,RMVar_hsa_circ_267084,RMVar_hsa_circ_114332,RMVar_hsa_circ_214566,RMVar_hsa_circ_265093,RMVar_hsa_circ_365393,RMVar_hsa_circ_360639,RMVar_hsa_circ_362344,RMVar_hsa_circ_346954,RMVar_hsa_circ_96540,RMVar_hsa_circ_30364,RMVar_hsa_circ_33074,RMVar_hsa_circ_214579,RMVar_hsa_circ_33472,RMVar_hsa_circ_338091,RMVar_hsa_circ_25792,RMVar_hsa_circ_338980,RMVar_hsa_circ_373365,RMVar_hsa_circ_286339,RMVar_hsa_circ_324950,RMVar_hsa_circ_41719,RMVar_hsa_circ_214582,RMVar_hsa_circ_214584,RMVar_hsa_circ_214585,RMVar_hsa_circ_214583,RMVar_hsa_circ_214581 5215 RMVar_ID_5215 Human_SNP_ID_704456724 A-to-I Human chr22 + 41156537 41156537 41156537 GAGTTCAGGAGTTGGAGACCAGCCTCACCAACATGGTGAAACCCCATCTCTACTAAAAATATAAA GAGTTCAGGAGTTGGAGACCAGCCTCACCAACGTGGTGAAACCCCATCTCTACTAAAAATATAAA A G EP300 Ensembl:ENSG00000100393 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs773330438 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_214543,RMVar_hsa_circ_61612,RMVar_hsa_circ_357085,RMVar_hsa_circ_357569,RMVar_hsa_circ_102183,RMVar_hsa_circ_214558,RMVar_hsa_circ_267084,RMVar_hsa_circ_114332,RMVar_hsa_circ_214566,RMVar_hsa_circ_265093,RMVar_hsa_circ_365393,RMVar_hsa_circ_360639,RMVar_hsa_circ_362344,RMVar_hsa_circ_346954,RMVar_hsa_circ_96540,RMVar_hsa_circ_30364,RMVar_hsa_circ_33074,RMVar_hsa_circ_214579,RMVar_hsa_circ_33472,RMVar_hsa_circ_338091,RMVar_hsa_circ_25792,RMVar_hsa_circ_338980,RMVar_hsa_circ_373365,RMVar_hsa_circ_286339,RMVar_hsa_circ_324950,RMVar_hsa_circ_41719,RMVar_hsa_circ_214582,RMVar_hsa_circ_214584,RMVar_hsa_circ_214585,RMVar_hsa_circ_214583,RMVar_hsa_circ_214581 5216 RMVar_ID_5216 Human_SNP_ID_704473724 A-to-I Human chr22 + 41211473 41211473 41211473 AGTGATCCCCCACCTCAGCCTCCCAAAGTGCTAGGATTACAGGCATGAGCCACCGCACCCAGCCC AGTGATCCCCCACCTCAGCCTCCCAAAGTGCTTGGATTACAGGCATGAGCCACCGCACCCAGCCC A T L3MBTL2 Ensembl:ENSG00000100395 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1479456686 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72377,RMVar_hsa_circ_107484,RMVar_hsa_circ_214598,RMVar_hsa_circ_56689 5217 RMVar_ID_5217 Human_SNP_ID_704475736 A-to-I Human chr22 + 41218419 41218419 41218419 CCTGTAATCCCAGCTACTTGGGAGGCCGAGACAGGAGAATCCCTTGAACCTGAGAGGCGGAGGTT CCTGTAATCCCAGCTACTTGGGAGGCCGAGACCGGAGAATCCCTTGAACCTGAGAGGCGGAGGTT A C L3MBTL2 Ensembl:ENSG00000100395 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946908136 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13377,RMVar_hsa_circ_107484,RMVar_hsa_circ_214598,RMVar_hsa_circ_56689,RMVar_hsa_circ_35460,RMVar_hsa_circ_214599,RMVar_hsa_circ_84741 5218 RMVar_ID_5218 Human_SNP_ID_704475820 A-to-I Human chr22 + 41218741 41218741 41218741 CCCCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCGGAGTAGCTGGGATTACAGGCATGTG CCCCTCCCAGGTTCAAGCGATTCTCCTGCCTCGGCCTCCGGAGTAGCTGGGATTACAGGCATGTG A G L3MBTL2 Ensembl:ENSG00000100395 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1169320631 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13377,RMVar_hsa_circ_107484,RMVar_hsa_circ_214598,RMVar_hsa_circ_56689,RMVar_hsa_circ_35460,RMVar_hsa_circ_214599,RMVar_hsa_circ_84741 5219 RMVar_ID_5219 Human_SNP_ID_704483664 A-to-I Human chr22 - 41244481 41244481 41244481 TCACCTGAGCCCAAGAAGTGGATGCTGCAGCAAGCCGTGATCGTGCCACTGCACTCCAGCATGAC TCACCTGAGCCCAAGAAGTGGATGCTGCAGCAGGCCGTGATCGTGCCACTGCACTCCAGCATGAC T C L13705-009,L13304-001 RNACentral:URS00001E2917,RNACentral:URS000044B5AA misc_RNA,scRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984723551 Functional Loss SNV dbSNP153 33..33 33 - - - 5220 RMVar_ID_5220 Human_SNP_ID_704487880 A-to-I Human chr22 - 41258792 41258792 41258792 AAATTAGTCGGGTGTGGTGGCGCACGCCTGTAATCTCAGCTACTCAGGAGGCTGAGGCAGGAGAA AAATTAGTCGGGTGTGGTGGCGCACGCCTGTAGTCTCAGCTACTCAGGAGGCTGAGGCAGGAGAA T C RANGAP1 Ensembl:ENSG00000100401 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs922171410 Functional Loss SNV dbSNP153 33..33 33 - - - 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 5221 RMVar_ID_5221 Human_SNP_ID_704488166 A-to-I Human chr22 - 41259884 41259884 41259884 CTCCCACCTCAGCCTCCCGATTAGCTGGGACTACAGGTGTGCACCACCATGCCCACCCAGTTAAT CTCCCACCTCAGCCTCCCGATTAGCTGGGACTGCAGGTGTGCACCACCATGCCCACCCAGTTAAT T C RANGAP1 Ensembl:ENSG00000100401 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs960672206 Functional Loss SNV dbSNP153 33..33 33 - - - 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 5222 RMVar_ID_5222 Human_SNP_ID_704488170 A-to-I Human chr22 - 41259894 41259894 41259894 TCAAGTGATCCTCCCACCTCAGCCTCCCGATTAGCTGGGACTACAGGTGTGCACCACCATGCCCA TCAAGTGATCCTCCCACCTCAGCCTCCCGATTCGCTGGGACTACAGGTGTGCACCACCATGCCCA T G RANGAP1 Ensembl:ENSG00000100401 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1227443424 Functional Loss SNV dbSNP153 33..33 33 - - - 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 5223 RMVar_ID_5223 Human_SNP_ID_704488203 A-to-I Human chr22 - 41260004 41260004 41260004 CCCTGAACCCAAAAAAAAAAAAAATTTTATTGAGGCAGGGTCTCGCTCTGTTGCCCAGGCTGGAG CCCTGAACCCAAAAAAAAAAAAAATTTTATTGCGGCAGGGTCTCGCTCTGTTGCCCAGGCTGGAG T G RANGAP1 Ensembl:ENSG00000100401 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1425437293 Functional Loss SNV dbSNP153 33..33 33 - - - 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 5224 RMVar_ID_5224 Human_SNP_ID_704490070 A-to-I Human chr22 - 41266716 41266716 41266716 CAGCCTGGCCAACATGCTGAAACCCTGTGTCTACAAAAGTACAAAAATTAGCTGGGCGTGATGGC CAGCCTGGCCAACATGCTGAAACCCTGTGTCTTCAAAAGTACAAAAATTAGCTGGGCGTGATGGC T A RANGAP1 Ensembl:ENSG00000100401 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1392727373 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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 5225 RMVar_ID_5225 Human_SNP_ID_704490205 A-to-I Human chr22 - 41267154 41267154 41267154 TCATTTCTGGCCAGGCGTGGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCCGAGGCGGGC TCATTTCTGGCCAGGCGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGC T C RANGAP1 Ensembl:ENSG00000100401 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs570010923 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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 5226 RMVar_ID_5226 Human_SNP_ID_704490249 A-to-I Human chr22 - 41267333 41267333 41267333 CGCCCAACCTCCTTTTATTTTTTTTTAAAGACAGGGTCTTGCTCTGTTGCCCAGGCTGGTCTTGA CGCCCAACCTCCTTTTATTTTTTTTTAAAGACGGGGTCTTGCTCTGTTGCCCAGGCTGGTCTTGA T C RANGAP1 Ensembl:ENSG00000100401 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1046356656 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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 5227 RMVar_ID_5227 Human_SNP_ID_704490250 A-to-I Human chr22 - 41267333 41267333 41267333 CGCCCAACCTCCTTTTATTTTTTTTTAAAGACAGGGTCTTGCTCTGTTGCCCAGGCTGGTCTTGA CGCCCAACCTCCTTTTATTTTTTTTTAAAGACCGGGTCTTGCTCTGTTGCCCAGGCTGGTCTTGA T G RANGAP1 Ensembl:ENSG00000100401 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1046356656 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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 5228 RMVar_ID_5228 Human_SNP_ID_704491944 A-to-I Human chr22 - 41273071 41273071 41273071 CCACGATCAGTCGGGCACGATGGCTCACAGCTATAATCCCAGCACTTTGGAAGGCCAAGGCCCAG CCACGATCAGTCGGGCACGATGGCTCACAGCTGTAATCCCAGCACTTTGGAAGGCCAAGGCCCAG T C RANGAP1 Ensembl:ENSG00000100401 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1230076756 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14504686 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 5229 RMVar_ID_5229 Human_SNP_ID_704492826 A-to-I Human chr22 - 41276403 41276403 41276403 AAACTCTTGACCTCAGGTGATCCTCAGGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG AAACTCTTGACCTCAGGTGATCCTCAGGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG T C RANGAP1 Ensembl:ENSG00000100401 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1315188534 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85248,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_214609,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_100108,RMVar_hsa_circ_335522,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,RMVar_hsa_circ_273308,RMVar_hsa_circ_214637 5230 RMVar_ID_5230 Human_SNP_ID_704493365 A-to-I Human chr22 - 41278097 41278097 41278097 GGGAGGCGGAGGTTGCAGTGAGCCGAGATGGCACCACTGTACTCCAGCCTCGGTGACAGAACGAG GGGAGGCGGAGGTTGCAGTGAGCCGAGATGGCCCCACTGTACTCCAGCCTCGGTGACAGAACGAG T G RANGAP1 Ensembl:ENSG00000100401 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941414594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25683182 RMVar_hsa_circ_85248,RMVar_hsa_circ_123402,RMVar_hsa_circ_94083,RMVar_hsa_circ_104363,RMVar_hsa_circ_214608,RMVar_hsa_circ_214609,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_100108,RMVar_hsa_circ_335522,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,RMVar_hsa_circ_273308,RMVar_hsa_circ_214637 5231 RMVar_ID_5231 Human_SNP_ID_704493584 A-to-I Human chr22 - 41278882 41278882 41278882 CTCTCACCTCGGCCTCCCAAAGTGTTGGGATTACAGGCGTGAGCCACCGTGCCCGGCCCCTTATT CTCTCACCTCGGCCTCCCAAAGTGTTGGGATTGCAGGCGTGAGCCACCGTGCCCGGCCCCTTATT T C RANGAP1 Ensembl:ENSG00000100401 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285948040 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85248,RMVar_hsa_circ_123402,RMVar_hsa_circ_94083,RMVar_hsa_circ_104363,RMVar_hsa_circ_214608,RMVar_hsa_circ_214609,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_100108,RMVar_hsa_circ_335522,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,RMVar_hsa_circ_273308,RMVar_hsa_circ_214637 5232 RMVar_ID_5232 Human_SNP_ID_704493726 A-to-I Human chr22 - 41279345 41279345 41279345 CTGCCTCAGCCTCCTGAGTAGCTAGGACTATAAGCACCCACCACCATGCTCCGCTAATTTTTTGT CTGCCTCAGCCTCCTGAGTAGCTAGGACTATAGGCACCCACCACCATGCTCCGCTAATTTTTTGT T C RANGAP1 Ensembl:ENSG00000100401 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1349712886 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14504910 RMVar_hsa_circ_85248,RMVar_hsa_circ_123402,RMVar_hsa_circ_94083,RMVar_hsa_circ_104363,RMVar_hsa_circ_214608,RMVar_hsa_circ_214609,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_100108,RMVar_hsa_circ_335522,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,RMVar_hsa_circ_273308,RMVar_hsa_circ_214637 5233 RMVar_ID_5233 Human_SNP_ID_704494462 A-to-I Human chr22 - 41282002 41282002 41282002 CTCCCACCTCAGCCTCCCCAGTGGCTGGGATTACTGGTGCACACCACCATACCCTGCTAATTGTA CTCCCACCTCAGCCTCCCCAGTGGCTGGGATTGCTGGTGCACACCACCATACCCTGCTAATTGTA T C RANGAP1 Ensembl:ENSG00000100401 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs1030938951 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85248,RMVar_hsa_circ_94083,RMVar_hsa_circ_214606,RMVar_hsa_circ_214607,RMVar_hsa_circ_81774,RMVar_hsa_circ_214628,RMVar_hsa_circ_104098,RMVar_hsa_circ_214636 5234 RMVar_ID_5234 Human_SNP_ID_704494517 A-to-I Human chr22 - 41282176 41282176 41282176 TGCCTCAGCCTCTCCAGTAGCTGGGACTGACTACAGGCACGTGCCACCACACCCAGCTAATTTTT TGCCTCAGCCTCTCCAGTAGCTGGGACTGACTGCAGGCACGTGCCACCACACCCAGCTAATTTTT T C RANGAP1 Ensembl:ENSG00000100401 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1399057158 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14505041 RMVar_hsa_circ_85248,RMVar_hsa_circ_94083,RMVar_hsa_circ_214606,RMVar_hsa_circ_214607,RMVar_hsa_circ_81774,RMVar_hsa_circ_214628,RMVar_hsa_circ_104098,RMVar_hsa_circ_214636 5235 RMVar_ID_5235 Human_SNP_ID_704494612 A-to-I Human chr22 - 41282444 41282444 41282444 ATGGTGGTGGGTGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATGACATGAACCTT ATGGTGGTGGGTGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGACATGAACCTT T C RANGAP1 Ensembl:ENSG00000100401 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1042086734 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85248,RMVar_hsa_circ_94083,RMVar_hsa_circ_214606,RMVar_hsa_circ_214607,RMVar_hsa_circ_81774,RMVar_hsa_circ_214628,RMVar_hsa_circ_104098,RMVar_hsa_circ_214636 5236 RMVar_ID_5236 Human_SNP_ID_704494617 A-to-I Human chr22 - 41282457 41282457 41282457 AAATTAGCTGGACATGGTGGTGGGTGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAA AAATTAGCTGGACATGGTGGTGGGTGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAA T C RANGAP1 Ensembl:ENSG00000100401 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1441752443 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85248,RMVar_hsa_circ_94083,RMVar_hsa_circ_214606,RMVar_hsa_circ_214607,RMVar_hsa_circ_81774,RMVar_hsa_circ_214628,RMVar_hsa_circ_104098,RMVar_hsa_circ_214636 5237 RMVar_ID_5237 Human_SNP_ID_704494628 A-to-I Human chr22 - 41282489 41282489 41282489 GGTGAAACCCTGTCTCTACTAAAAATACAAAAAAATTAGCTGGACATGGTGGTGGGTGCCTGTAA GGTGAAACCCTGTCTCTACTAAAAATACAAAATAATTAGCTGGACATGGTGGTGGGTGCCTGTAA T A RANGAP1 Ensembl:ENSG00000100401 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1467164685 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85248,RMVar_hsa_circ_94083,RMVar_hsa_circ_214606,RMVar_hsa_circ_214607,RMVar_hsa_circ_81774,RMVar_hsa_circ_214628,RMVar_hsa_circ_104098,RMVar_hsa_circ_214636 5238 RMVar_ID_5238 Human_SNP_ID_704494654 A-to-I Human chr22 - 41282594 41282594 41282594 TTATTGGCCAAGCGTGGTGGCTCATGCGTGTAATCCCAGCACTTTGGGAGGCTGAGGCGAGTGGA TTATTGGCCAAGCGTGGTGGCTCATGCGTGTATTCCCAGCACTTTGGGAGGCTGAGGCGAGTGGA T A RANGAP1 Ensembl:ENSG00000100401 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1361750387 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14541012,Human_RBP_ID_20768522 RMVar_hsa_circ_85248,RMVar_hsa_circ_94083,RMVar_hsa_circ_214606,RMVar_hsa_circ_214607,RMVar_hsa_circ_104098,RMVar_hsa_circ_214636 5239 RMVar_ID_5239 Human_SNP_ID_704495043 A-to-I Human chr22 - 41283998 41283998 41283998 GTGATCCGCCCACCTCAGCCTCCCAAAGTACTAGGATTATAGGTGTGAGCCTTTGCGCCCGGCCC GTGATCCGCCCACCTCAGCCTCCCAAAGTACTGGGATTATAGGTGTGAGCCTTTGCGCCCGGCCC T C RANGAP1 Ensembl:ENSG00000100401 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053881342 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14505143 RMVar_hsa_circ_85248,RMVar_hsa_circ_94083,RMVar_hsa_circ_214606,RMVar_hsa_circ_214607,RMVar_hsa_circ_104098,RMVar_hsa_circ_214636 5240 RMVar_ID_5240 Human_SNP_ID_704495044 A-to-I Human chr22 - 41283998 41283998 41283998 GTGATCCGCCCACCTCAGCCTCCCAAAGTACTAGGATTATAGGTGTGAGCCTTTGCGCCCGGCCC GTGATCCGCCCACCTCAGCCTCCCAAAGTACTCGGATTATAGGTGTGAGCCTTTGCGCCCGGCCC T G RANGAP1 Ensembl:ENSG00000100401 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053881342 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14505143 RMVar_hsa_circ_85248,RMVar_hsa_circ_94083,RMVar_hsa_circ_214606,RMVar_hsa_circ_214607,RMVar_hsa_circ_104098,RMVar_hsa_circ_214636 5241 RMVar_ID_5241 Human_SNP_ID_704495081 A-to-I Human chr22 - 41284125 41284102 41284125 CTCTTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCCCCCGCCACCAGGCCCGGCTAATTTTT CTCTTGCCTCAGCCTCCCGAGTAGCTGGGACT_______________________GCTAATTTTT CCGGGCCTGGTGGCGGGGGCCTGT C RANGAP1 Ensembl:ENSG00000100401 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1157154906 Functional Loss DEL dbSNP153 33..55 33 - - - RMVar_hsa_circ_85248,RMVar_hsa_circ_94083,RMVar_hsa_circ_214606,RMVar_hsa_circ_214607,RMVar_hsa_circ_104098,RMVar_hsa_circ_214636 5242 RMVar_ID_5242 Human_SNP_ID_704495094 A-to-I Human chr22 - 41284125 41284125 41284125 CTCTTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCCCCCGCCACCAGGCCCGGCTAATTTTT CTCTTGCCTCAGCCTCCCGAGTAGCTGGGACTGCAGGCCCCCGCCACCAGGCCCGGCTAATTTTT T C RANGAP1 Ensembl:ENSG00000100401 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs566707522 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85248,RMVar_hsa_circ_94083,RMVar_hsa_circ_214606,RMVar_hsa_circ_214607,RMVar_hsa_circ_104098,RMVar_hsa_circ_214636 5243 RMVar_ID_5243 Human_SNP_ID_704499053 A-to-I Human chr22 - 41296960 41296960 41296960 GTGATCTGTCCGCCTCGGCCTCCCAAAGTGCTAGGATTATAGGCCTGAGCCACTGCGCCCAGTCG GTGATCTGTCCGCCTCGGCCTCCCAAAGTGCTGGGATTATAGGCCTGAGCCACTGCGCCCAGTCG T C L13705-009,L13304-001 RNACentral:URS00001E2917,RNACentral:URS000044B5AA misc_RNA,scRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1344580316 Functional Loss SNV dbSNP153 33..33 33 - - - 5244 RMVar_ID_5244 Human_SNP_ID_704509976 A-to-I Human chr22 + 41337993 41337993 41337993 GGGTTCAAACCATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGGTTACAGGCTCCTGCCACCATG GGGTTCAAACCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGGTTACAGGCTCCTGCCACCATG A G ZC3H7B Ensembl:ENSG00000100403 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs879908355 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101564,RMVar_hsa_circ_268550,RMVar_hsa_circ_214638,RMVar_hsa_circ_99618,RMVar_hsa_circ_93662,RMVar_hsa_circ_81532,RMVar_hsa_circ_214641,RMVar_hsa_circ_109932,RMVar_hsa_circ_214642,RMVar_hsa_circ_100415,RMVar_hsa_circ_117936,RMVar_hsa_circ_214643,RMVar_hsa_circ_301352,RMVar_hsa_circ_110549,RMVar_hsa_circ_95694,RMVar_hsa_circ_214645,RMVar_hsa_circ_214647,RMVar_hsa_circ_17376,RMVar_hsa_circ_214648,RMVar_hsa_circ_214646,RMVar_hsa_circ_214644 5245 RMVar_ID_5245 Human_SNP_ID_704511951 A-to-I Human chr22 + 41344945 41344945 41344945 TTCTTGCCTCAGCCTCTTGAGTAGCTGAGACTACAGGCACATGCCACCACACCCAGCTTATTCTT TTCTTGCCTCAGCCTCTTGAGTAGCTGAGACTGCAGGCACATGCCACCACACCCAGCTTATTCTT A G ZC3H7B Ensembl:ENSG00000100403 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1487359352 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268550,RMVar_hsa_circ_99618,RMVar_hsa_circ_93662,RMVar_hsa_circ_214641,RMVar_hsa_circ_110549,RMVar_hsa_circ_95694,RMVar_hsa_circ_214645,RMVar_hsa_circ_214646,RMVar_hsa_circ_78802,RMVar_hsa_circ_347139,RMVar_hsa_circ_214644,RMVar_hsa_circ_360233,RMVar_hsa_circ_214650,RMVar_hsa_circ_97772,RMVar_hsa_circ_214654,RMVar_hsa_circ_93732,RMVar_hsa_circ_214655 5246 RMVar_ID_5246 Human_SNP_ID_704520087 A-to-I Human chr22 + 41374605 41374605 41374605 AGGCAAGGCAGTGCACACCTGAAATCCGAGCTACTCTGGAGGCTGGGGCAGGAGGATTGCTTGAG AGGCAAGGCAGTGCACACCTGAAATCCGAGCTGCTCTGGAGGCTGGGGCAGGAGGATTGCTTGAG A G TEF Ensembl:ENSG00000167074 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1347558918 Functional Loss SNV dbSNP153 33..33 33 - - - 5247 RMVar_ID_5247 Human_SNP_ID_704532038 A-to-I Human chr22 + 41415177 41415177 41415177 TCGGTTCACTGCAACCGCCACCTCCCGGGTTCAAGCGATTCTCCTGCCTCGGCCTCTCTAGTAGC TCGGTTCACTGCAACCGCCACCTCCCGGGTTCGAGCGATTCTCCTGCCTCGGCCTCTCTAGTAGC A G lnc-TEF-1,lnc-TEF-1:2 RNACentral:URS00009B15C0,RNACentral:URS00008B60BA lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1323354894 Functional Loss SNV dbSNP153 33..33 33 - - - 5248 RMVar_ID_5248 Human_SNP_ID_704532251 A-to-I Human chr22 + 41416052 41416052 41416052 CACAGTACTGGGGGCTGGGCGCGGTGGCTGACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGC CACAGTACTGGGGGCTGGGCGCGGTGGCTGACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGC A G lnc-TEF-1,lnc-TEF-1:2 RNACentral:URS00009B15C0,RNACentral:URS00008B60BA lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1304249414 Functional Loss SNV dbSNP153 33..33 33 - - - 5249 RMVar_ID_5249 Human_SNP_ID_704533819 A-to-I Human chr22 + 41421611 41421611 41421611 CCACGCCCACCTAATTTTTATATTTTTTGTAGAAATGGTGTTTTACTGTCTTGCCCAGGCTGGTC CCACGCCCACCTAATTTTTATATTTTTTGTAGGAATGGTGTTTTACTGTCTTGCCCAGGCTGGTC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982116964 Functional Loss SNV dbSNP153 33..33 33 - - - 5250 RMVar_ID_5250 Human_SNP_ID_704533821 A-to-I Human chr22 + 41421623 41421623 41421623 AATTTTTATATTTTTTGTAGAAATGGTGTTTTACTGTCTTGCCCAGGCTGGTCTTGAACTCCTGA AATTTTTATATTTTTTGTAGAAATGGTGTTTTGCTGTCTTGCCCAGGCTGGTCTTGAACTCCTGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025582076 Functional Loss SNV dbSNP153 33..33 33 - - - 5251 RMVar_ID_5251 Human_SNP_ID_704536237 A-to-I Human chr22 + 41431027 41431027 41431027 ATGTATTTATTTATTCATTTAGCGATCCTCCTACCTCAGCCTCCAGAGTAGCTGGGACACAGGTA ATGTATTTATTTATTCATTTAGCGATCCTCCTGCCTCAGCCTCCAGAGTAGCTGGGACACAGGTA A G AL008582.1 Ensembl:ENSG00000273424 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs923478905 Functional Loss SNV dbSNP153 33..33 33 - - - 5252 RMVar_ID_5252 Human_SNP_ID_704536239 A-to-I Human chr22 + 41431044 41431044 41431044 TTTAGCGATCCTCCTACCTCAGCCTCCAGAGTAGCTGGGACACAGGTATGCGCCACCACACTCGG TTTAGCGATCCTCCTACCTCAGCCTCCAGAGTGGCTGGGACACAGGTATGCGCCACCACACTCGG A G AL008582.1 Ensembl:ENSG00000273424 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1376669007 Functional Loss SNV dbSNP153 33..33 33 - - - 5253 RMVar_ID_5253 Human_SNP_ID_704539496 A-to-I Human chr22 - 41443460 41443460 41443460 CAAAAATTAGCCGGGCGTGGTCCCGCGTGCCTATAATCCCAGCTACTCGGGAGGCTGAGGCGGGA CAAAAATTAGCCGGGCGTGGTCCCGCGTGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCGGGA T C TOB2 Ensembl:ENSG00000183864 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1344695518 Functional Loss SNV dbSNP153 33..33 33 - - - 5254 RMVar_ID_5254 Human_SNP_ID_704539513 A-to-I Human chr22 - 41443484 41443483 41443484 GAAGCCCCGTCTCTACTAAAAATACAAAAATTAGCCGGGCGTGGTCCCGCGTGCCTATAATCCCA GAAGCCCCGTCTCTACTAAAAATACAAAAATT_GCCGGGCGTGGTCCCGCGTGCCTATAATCCCA CT C TOB2 Ensembl:ENSG00000183864 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1201491121 Functional Loss DEL dbSNP153 33..33 33 - - - 5255 RMVar_ID_5255 Human_SNP_ID_704539819 A-to-I Human chr22 - 41444403 41444403 41444403 CCGCCTACGTTTGGGTTGAGTCGAGTTTTCCTAGCTCCTGAGGAACATGGAGTGCCCTAGAAAGG CCGCCTACGTTTGGGTTGAGTCGAGTTTTCCTGGCTCCTGAGGAACATGGAGTGCCCTAGAAAGG T C TOB2 Ensembl:ENSG00000183864 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs106860 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8551374,Human_RBP_ID_14505912,Human_RBP_ID_25674785 GWAS_ID_189,GWAS_ID_190,GWAS_ID_191,GWAS_ID_192,GWAS_ID_193,GWAS_ID_194,GWAS_ID_195 5256 RMVar_ID_5256 Human_SNP_ID_704544612 A-to-I Human chr22 - 41460111 41460111 41460111 TCGAGAAGCAAAGATCTGTTCTCCATATTGGTATGTTCTCCCTCAACCAAGATCTTCTAAAAAGA TCGAGAAGCAAAGATCTGTTCTCCATATTGGTGTGTTCTCCCTCAACCAAGATCTTCTAAAAAGA T C PHF5A Ensembl:ENSG00000100410 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs922873698 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_581525,Human_RBP_ID_1612681,Human_RBP_ID_14506060,Human_RBP_ID_17702145,Human_RBP_ID_17987262,Human_RBP_ID_27309051,Human_RBP_ID_27494717 RMVar_hsa_circ_75997,RMVar_hsa_circ_98699,RMVar_hsa_circ_88245,RMVar_hsa_circ_214663,RMVar_hsa_circ_214664,RMVar_hsa_circ_214665,RMVar_hsa_circ_214662,RMVar_hsa_circ_378703 5257 RMVar_ID_5257 Human_SNP_ID_704545158 A-to-I Human chr22 - 41462031 41462031 41462031 TCTAGCCAGTAGTGCTCTGTACCCCCAAGACCATGTGTCAAATTAAGTGAATTAATGAAGACACA TCTAGCCAGTAGTGCTCTGTACCCCCAAGACCGTGTGTCAAATTAAGTGAATTAATGAAGACACA T C PHF5A Ensembl:ENSG00000100410 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs5751108 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14506082 GWAS_ID_196,GWAS_ID_197,GWAS_ID_198,GWAS_ID_199 RMVar_hsa_circ_75997,RMVar_hsa_circ_98699,RMVar_hsa_circ_88245,RMVar_hsa_circ_214663,RMVar_hsa_circ_214664,RMVar_hsa_circ_214662 5258 RMVar_ID_5258 Human_SNP_ID_704545516 A-to-I Human chr22 - 41463506 41463506 41463506 GGCTAGGCTGATCTTGAACTCCTGACCTTGTGATCCACCCACCTTGGCCTCCCAAAGTTGCTGGG GGCTAGGCTGATCTTGAACTCCTGACCTTGTGGTCCACCCACCTTGGCCTCCCAAAGTTGCTGGG T C PHF5A Ensembl:ENSG00000100410 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1379178195 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75997,RMVar_hsa_circ_98699,RMVar_hsa_circ_88245,RMVar_hsa_circ_214663,RMVar_hsa_circ_214664,RMVar_hsa_circ_214662 5259 RMVar_ID_5259 Human_SNP_ID_704545529 A-to-I Human chr22 - 41463552 41463552 41463552 CCTGGCTAATTTTTTGTTTTTAGTAGAGACAGAGTTTCACCATGTTGGCTAGGCTGATCTTGAAC CCTGGCTAATTTTTTGTTTTTAGTAGAGACAGTGTTTCACCATGTTGGCTAGGCTGATCTTGAAC T A PHF5A Ensembl:ENSG00000100410 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6002385 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75997,RMVar_hsa_circ_98699,RMVar_hsa_circ_88245,RMVar_hsa_circ_214663,RMVar_hsa_circ_214664,RMVar_hsa_circ_214662 5260 RMVar_ID_5260 Human_SNP_ID_704545530 A-to-I Human chr22 - 41463552 41463552 41463552 CCTGGCTAATTTTTTGTTTTTAGTAGAGACAGAGTTTCACCATGTTGGCTAGGCTGATCTTGAAC CCTGGCTAATTTTTTGTTTTTAGTAGAGACAGGGTTTCACCATGTTGGCTAGGCTGATCTTGAAC T C PHF5A Ensembl:ENSG00000100410 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6002385 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75997,RMVar_hsa_circ_98699,RMVar_hsa_circ_88245,RMVar_hsa_circ_214663,RMVar_hsa_circ_214664,RMVar_hsa_circ_214662 5261 RMVar_ID_5261 Human_SNP_ID_704545531 A-to-I Human chr22 - 41463552 41463552 41463552 CCTGGCTAATTTTTTGTTTTTAGTAGAGACAGAGTTTCACCATGTTGGCTAGGCTGATCTTGAAC CCTGGCTAATTTTTTGTTTTTAGTAGAGACAGCGTTTCACCATGTTGGCTAGGCTGATCTTGAAC T G PHF5A Ensembl:ENSG00000100410 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6002385 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75997,RMVar_hsa_circ_98699,RMVar_hsa_circ_88245,RMVar_hsa_circ_214663,RMVar_hsa_circ_214664,RMVar_hsa_circ_214662 5262 RMVar_ID_5262 Human_SNP_ID_704545535 A-to-I Human chr22 - 41463563 41463563 41463563 GCACCACCACGCCTGGCTAATTTTTTGTTTTTAGTAGAGACAGAGTTTCACCATGTTGGCTAGGC GCACCACCACGCCTGGCTAATTTTTTGTTTTTGGTAGAGACAGAGTTTCACCATGTTGGCTAGGC T C PHF5A Ensembl:ENSG00000100410 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1468581292 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75997,RMVar_hsa_circ_98699,RMVar_hsa_circ_88245,RMVar_hsa_circ_214663,RMVar_hsa_circ_214664,RMVar_hsa_circ_214662 5263 RMVar_ID_5263 Human_SNP_ID_704545635 A-to-I Human chr22 - 41463818 41463818 41463818 ACGATCTCGGCTCATTACAATCTCCGCCTCCCAGGTTCAAGCGATTCTCCTGCCTAAGCTTCCCA ACGATCTCGGCTCATTACAATCTCCGCCTCCCGGGTTCAAGCGATTCTCCTGCCTAAGCTTCCCA T C PHF5A Ensembl:ENSG00000100410 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1013663474 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25674849 RMVar_hsa_circ_75997,RMVar_hsa_circ_98699,RMVar_hsa_circ_88245,RMVar_hsa_circ_214663,RMVar_hsa_circ_214664,RMVar_hsa_circ_214662 5264 RMVar_ID_5264 Human_SNP_ID_704545964 A-to-I Human chr22 - 41465366 41465366 41465366 CTGAGGTCAGGAGTTTGAGAGCAGCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATACG CTGAGGTCAGGAGTTTGAGAGCAGCCTGGCCAGCATGGTGAAACCCCGTCTCTACTAAAAATACG T C PHF5A Ensembl:ENSG00000100410 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs959889219 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75997,RMVar_hsa_circ_98699,RMVar_hsa_circ_88245,RMVar_hsa_circ_214663,RMVar_hsa_circ_214664,RMVar_hsa_circ_214662 5265 RMVar_ID_5265 Human_SNP_ID_704546184 A-to-I Human chr22 - 41466284 41466284 41466284 AACTCTGAGCCAAATGCCAGGAGAGAGAGCTTATAGACTAGTGCTACAGGCAAGATTTACCCCAT AACTCTGAGCCAAATGCCAGGAGAGAGAGCTTTTAGACTAGTGCTACAGGCAAGATTTACCCCAT T A PHF5A Ensembl:ENSG00000100410 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs5758368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14506163 GWAS_ID_200,GWAS_ID_201,GWAS_ID_202,GWAS_ID_203,GWAS_ID_204 RMVar_hsa_circ_75997,RMVar_hsa_circ_98699,RMVar_hsa_circ_88245,RMVar_hsa_circ_214663,RMVar_hsa_circ_214664,RMVar_hsa_circ_214662 5266 RMVar_ID_5266 Human_SNP_ID_704546185 A-to-I Human chr22 - 41466284 41466284 41466284 AACTCTGAGCCAAATGCCAGGAGAGAGAGCTTATAGACTAGTGCTACAGGCAAGATTTACCCCAT AACTCTGAGCCAAATGCCAGGAGAGAGAGCTTGTAGACTAGTGCTACAGGCAAGATTTACCCCAT T C PHF5A Ensembl:ENSG00000100410 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs5758368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14506163 GWAS_ID_200,GWAS_ID_201,GWAS_ID_202,GWAS_ID_203,GWAS_ID_204 RMVar_hsa_circ_75997,RMVar_hsa_circ_98699,RMVar_hsa_circ_88245,RMVar_hsa_circ_214663,RMVar_hsa_circ_214664,RMVar_hsa_circ_214662 5267 RMVar_ID_5267 Human_SNP_ID_704546343 A-to-I Human chr22 - 41466992 41466992 41466992 TTGTTTTTTGCTTCTTGTTTTTTGTTTTTTTGAGATGGGGTCTCTTGCTCTGTGGCCCAGGCTGG TTGTTTTTTGCTTCTTGTTTTTTGTTTTTTTGTGATGGGGTCTCTTGCTCTGTGGCCCAGGCTGG T A PHF5A Ensembl:ENSG00000100410 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs539985949 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75997,RMVar_hsa_circ_98699,RMVar_hsa_circ_88245,RMVar_hsa_circ_214663,RMVar_hsa_circ_214664,RMVar_hsa_circ_214662 5268 RMVar_ID_5268 Human_SNP_ID_704554865 A-to-I Human chr22 + 41500585 41500585 41500585 TTTTGTAGTTTTAGTAGAGATGGGGTTTTGCCATGTTGCCCAGGCTGGTCTCGAATTCCTGAGCT TTTTGTAGTTTTAGTAGAGATGGGGTTTTGCCGTGTTGCCCAGGCTGGTCTCGAATTCCTGAGCT A G ACO2 Ensembl:ENSG00000100412 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs970588583 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108181,RMVar_hsa_circ_117404,RMVar_hsa_circ_214667,RMVar_hsa_circ_80756,RMVar_hsa_circ_214666,RMVar_hsa_circ_314363,RMVar_hsa_circ_214668 5269 RMVar_ID_5269 Human_SNP_ID_704555295 A-to-I Human chr22 + 41502702 41502702 41502702 GCAATCTCGGCTCACTGCAACCTCCACCTCCCAGGCTCAAGCGATTGTCCTGCCTCAGCCTCCTG GCAATCTCGGCTCACTGCAACCTCCACCTCCCCGGCTCAAGCGATTGTCCTGCCTCAGCCTCCTG A C ACO2 Ensembl:ENSG00000100412 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1280260532 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108181,RMVar_hsa_circ_117404,RMVar_hsa_circ_214667,RMVar_hsa_circ_80756,RMVar_hsa_circ_214666,RMVar_hsa_circ_314363,RMVar_hsa_circ_214668 5270 RMVar_ID_5270 Human_SNP_ID_704555518 A-to-I Human chr22 + 41503572 41503572 41503572 GGGATGGTCTCAATCTCCTGACCTTGTGATCCACCCGCCTCAGTCTCCCAAAGTGCTGAGGTGAC GGGATGGTCTCAATCTCCTGACCTTGTGATCCCCCCGCCTCAGTCTCCCAAAGTGCTGAGGTGAC A C ACO2 Ensembl:ENSG00000100412 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs952163281 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108181,RMVar_hsa_circ_117404,RMVar_hsa_circ_214667,RMVar_hsa_circ_80756,RMVar_hsa_circ_214666,RMVar_hsa_circ_314363,RMVar_hsa_circ_214668 5271 RMVar_ID_5271 Human_SNP_ID_704555519 A-to-I Human chr22 + 41503572 41503572 41503572 GGGATGGTCTCAATCTCCTGACCTTGTGATCCACCCGCCTCAGTCTCCCAAAGTGCTGAGGTGAC GGGATGGTCTCAATCTCCTGACCTTGTGATCCGCCCGCCTCAGTCTCCCAAAGTGCTGAGGTGAC A G ACO2 Ensembl:ENSG00000100412 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs952163281 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108181,RMVar_hsa_circ_117404,RMVar_hsa_circ_214667,RMVar_hsa_circ_80756,RMVar_hsa_circ_214666,RMVar_hsa_circ_314363,RMVar_hsa_circ_214668 5272 RMVar_ID_5272 Human_SNP_ID_704555873 A-to-I Human chr22 + 41504779 41504779 41504779 AGGGTCTTGCTCTGTTACCCAGGCTGGAGTGCAGTGGTTCGATCATGGCTTACTGCAGCCTTGAC AGGGTCTTGCTCTGTTACCCAGGCTGGAGTGCGGTGGTTCGATCATGGCTTACTGCAGCCTTGAC A G ACO2 Ensembl:ENSG00000100412 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1268070257 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108181,RMVar_hsa_circ_117404,RMVar_hsa_circ_214667,RMVar_hsa_circ_80756,RMVar_hsa_circ_214666,RMVar_hsa_circ_314363,RMVar_hsa_circ_214668 5273 RMVar_ID_5273 Human_SNP_ID_704555887 A-to-I Human chr22 + 41504853 41504853 41504853 TCAATCCATCCTCCCACCTCAGCCTTCCCAGTATCTGGGACTATAGGCACATGCCACCATGCCTG TCAATCCATCCTCCCACCTCAGCCTTCCCAGTGTCTGGGACTATAGGCACATGCCACCATGCCTG A G ACO2 Ensembl:ENSG00000100412 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1371846375 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108181,RMVar_hsa_circ_117404,RMVar_hsa_circ_214667,RMVar_hsa_circ_80756,RMVar_hsa_circ_214666,RMVar_hsa_circ_314363,RMVar_hsa_circ_214668 5274 RMVar_ID_5274 Human_SNP_ID_704555891 A-to-I Human chr22 + 41504863 41504863 41504863 CTCCCACCTCAGCCTTCCCAGTATCTGGGACTATAGGCACATGCCACCATGCCTGGCTTCTTTTT CTCCCACCTCAGCCTTCCCAGTATCTGGGACTGTAGGCACATGCCACCATGCCTGGCTTCTTTTT A G ACO2 Ensembl:ENSG00000100412 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1380918425 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108181,RMVar_hsa_circ_117404,RMVar_hsa_circ_214667,RMVar_hsa_circ_80756,RMVar_hsa_circ_214666,RMVar_hsa_circ_314363,RMVar_hsa_circ_214668 5275 RMVar_ID_5275 Human_SNP_ID_704555981 A-to-I Human chr22 + 41505297 41505297 41505297 TAAAATTAGCCAATGTGGTGGTGCGTGCCTATAATCCCAGTTACTCAGAGGCTGAGGTGGGAGGA TAAAATTAGCCAATGTGGTGGTGCGTGCCTATGATCCCAGTTACTCAGAGGCTGAGGTGGGAGGA A G ACO2 Ensembl:ENSG00000100412 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1160667616 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108181,RMVar_hsa_circ_117404,RMVar_hsa_circ_214667,RMVar_hsa_circ_80756,RMVar_hsa_circ_214666,RMVar_hsa_circ_314363,RMVar_hsa_circ_214668 5276 RMVar_ID_5276 Human_SNP_ID_704555996 A-to-I Human chr22 + 41505368 41505368 41505368 GAGCCTGAAAGGTTGAGGCTGCAGTGAGCTACAATTGTGCCACTACACTCCAGCCTGGGTGACAG GAGCCTGAAAGGTTGAGGCTGCAGTGAGCTACGATTGTGCCACTACACTCCAGCCTGGGTGACAG A G ACO2 Ensembl:ENSG00000100412 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1221552475 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108181,RMVar_hsa_circ_117404,RMVar_hsa_circ_214667,RMVar_hsa_circ_80756,RMVar_hsa_circ_214666,RMVar_hsa_circ_314363,RMVar_hsa_circ_214668 5277 RMVar_ID_5277 Human_SNP_ID_704562590 A-to-I Human chr22 - 41528942 41528942 41528942 TGGTTTTGGATTCTTGTTTTCCTTGCAAGAACAAAAGGTTCTCTAGAATCCTTCAGCCACCAATG TGGTTTTGGATTCTTGTTTTCCTTGCAAGAACGAAAGGTTCTCTAGAATCCTTCAGCCACCAATG T C POLR3H Ensembl:ENSG00000100413 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1286916638 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1943726,Human_RBP_ID_17515498,Human_RBP_ID_17987326,Human_RBP_ID_22085661,Human_RBP_ID_27039073,Human_RBP_ID_27309132 Human_miRNA_ID_1133568,Human_miRNA_ID_2798116,Human_miRNA_ID_2798117,Human_miRNA_ID_2799080,Human_miRNA_ID_2799081,Human_miRNA_ID_2800463,Human_miRNA_ID_2800464,Human_miRNA_ID_2807776,Human_miRNA_ID_2807777,Human_miRNA_ID_2810920,Human_miRNA_ID_2810921,Human_miRNA_ID_2814062,Human_miRNA_ID_2814063,Human_miRNA_ID_2833654,Human_miRNA_ID_2833655,Human_miRNA_ID_2853175,Human_miRNA_ID_2853176,Human_miRNA_ID_2854237,Human_miRNA_ID_2854238,Human_miRNA_ID_2861321,Human_miRNA_ID_2861322,Human_miRNA_ID_2876133,Human_miRNA_ID_2876134,Human_miRNA_ID_2928397,Human_miRNA_ID_2928398 RMVar_hsa_circ_214684,RMVar_hsa_circ_84127,RMVar_hsa_circ_214685,RMVar_hsa_circ_377486 5278 RMVar_ID_5278 Human_SNP_ID_704564337 A-to-I Human chr22 + 41534628 41534628 41534628 ACGCTGTGGAATGGCCCCGCGCACGGTGGCTCAAGTCTGTAATCCCAGCACTTTGGGAGGTCGAG ACGCTGTGGAATGGCCCCGCGCACGGTGGCTCGAGTCTGTAATCCCAGCACTTTGGGAGGTCGAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1286389166 Functional Loss SNV dbSNP153 33..33 33 - - - 5279 RMVar_ID_5279 Human_SNP_ID_704565422 A-to-I Human chr22 - 41538487 41538487 41538487 GGGAGGTAAAGGCGGGTGCATCACCTGAGGTCAGGAGTTCTAGACCAGCCTGGCCAACATGGCAA GGGAGGTAAAGGCGGGTGCATCACCTGAGGTCGGGAGTTCTAGACCAGCCTGGCCAACATGGCAA T C POLR3H Ensembl:ENSG00000100413 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1486401549 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_214685,RMVar_hsa_circ_377486,RMVar_hsa_circ_299866,RMVar_hsa_circ_214688 5280 RMVar_ID_5280 Human_SNP_ID_704565559 A-to-I Human chr22 - 41539018 41539017 41539018 GACCTCGTGATCCGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCCCC GACCTCGTGATCCGCCCACCTCGGCCTCCCAA_GTGCTGGGATTACAGGCGTGAGCCACTGCCCC CT C POLR3H Ensembl:ENSG00000100413 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1425182247 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_214685,RMVar_hsa_circ_377486,RMVar_hsa_circ_299866,RMVar_hsa_circ_214688 5281 RMVar_ID_5281 Human_SNP_ID_704578400 A-to-I Human chr22 - 41586148 41586148 41586148 AGGTGGCCGCCTTCCTGCAGAAGCTACGAAGTAGAGTGCAGATCGGTGTGGTGGGCGGCTCTGAC AGGTGGCCGCCTTCCTGCAGAAGCTACGAAGTCGAGTGCAGATCGGTGTGGTGGGCGGCTCTGAC T G PMM1 Ensembl:ENSG00000100417 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs762507816 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_782057,Human_RBP_ID_4709113,Human_RBP_ID_14507375 Human_Splice_Rec_2170954,Human_Splice_Rec_2170955,Human_Splice_Rec_2170982,Human_Splice_Rec_2170983,Human_Splice_Rec_2170994,Human_Splice_Rec_2170995,Human_Splice_Rec_2171008,Human_Splice_Rec_2171009,Human_Splice_Rec_2171016,Human_Splice_Rec_2171017,Human_Splice_Rec_2171022,Human_Splice_Rec_2171023,Human_Splice_Rec_2171030 RMVar_hsa_circ_17915,RMVar_hsa_circ_309282 5282 RMVar_ID_5282 Human_SNP_ID_704578998 A-to-I Human chr22 - 41588331 41588331 41588331 CCTGTAATCCTAGCTAGTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCCGAGAGGCAGAAGTT CCTGTAATCCTAGCTAGTCGGGAGGCTGAGGCGGGAGAATCACTTGAACCCGAGAGGCAGAAGTT T C PMM1 Ensembl:ENSG00000100417 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs550198653 Functional Loss SNV dbSNP153 33..33 33 - - - 5283 RMVar_ID_5283 Human_SNP_ID_704579834 A-to-I Human chr22 - 41590928 41590928 41590928 ATAAAATAAAATAAACATAAAAGTAAGTAAAAATACAAAAATTAGGTGGGCATGGTGGCACACGC ATAAAATAAAATAAACATAAAAGTAAGTAAAAGTACAAAAATTAGGTGGGCATGGTGGCACACGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1238721028 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2720393 5284 RMVar_ID_5284 Human_SNP_ID_704579880 A-to-I Human chr22 - 41591123 41591123 41591123 AAAATTAGCCGGGCGTGGTGGCGCACTTCTGTAGTTTCAGCTACTCAGGAGGCTGAGGCAGGAGA AAAATTAGCCGGGCGTGGTGGCGCACTTCTGTGGTTTCAGCTACTCAGGAGGCTGAGGCAGGAGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1244073391 Functional Loss SNV dbSNP153 33..33 33 - - - 5285 RMVar_ID_5285 Human_SNP_ID_704581191 A-to-I Human chr22 - 41595003 41595003 41595003 CAACCTCTGGGTTCATGCGATGCTCCTGCCTCAGTCACCTGAGTAGCTGGGATTACAGGCATGCG CAACCTCTGGGTTCATGCGATGCTCCTGCCTCGGTCACCTGAGTAGCTGGGATTACAGGCATGCG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs762899633 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14507524 5286 RMVar_ID_5286 Human_SNP_ID_704582158 A-to-I Human chr22 - 41599288 41599288 41599288 TTAGTTAGATTTTGGGAAAGTGAGCATGAAGAAGGGACTCAGAGCTGCCAGGTACCCGAGTCTCA TTAGTTAGATTTTGGGAAAGTGAGCATGAAGAGGGGACTCAGAGCTGCCAGGTACCCGAGTCTCA T C DESI1 Ensembl:ENSG00000100418 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs11552897 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_581617,Human_RBP_ID_1943765,Human_RBP_ID_7087240,Human_RBP_ID_14507703 Human_miRNA_ID_544884,Human_miRNA_ID_580119,Human_miRNA_ID_583088,Human_miRNA_ID_2211001 RMVar_hsa_circ_100552,RMVar_hsa_circ_108119,RMVar_hsa_circ_110812,RMVar_hsa_circ_214696,RMVar_hsa_circ_214697,RMVar_hsa_circ_214698 5287 RMVar_ID_5287 Human_SNP_ID_704582221 A-to-I Human chr22 - 41599582 41599582 41599582 GCACTCCAGCCTGGGCGACAGAGTGAGACTCCATCTCAAAAAAATAAAATAATGAAGTGGAATCA GCACTCCAGCCTGGGCGACAGAGTGAGACTCCGTCTCAAAAAAATAAAATAATGAAGTGGAATCA T C DESI1 Ensembl:ENSG00000100418 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1239271043 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26499006 RMVar_hsa_circ_100552,RMVar_hsa_circ_108119,RMVar_hsa_circ_110812,RMVar_hsa_circ_214696,RMVar_hsa_circ_214697,RMVar_hsa_circ_214698 5288 RMVar_ID_5288 Human_SNP_ID_704582222 A-to-I Human chr22 - 41599589 41599588 41599589 TACCAGTGCACTCCAGCCTGGGCGACAGAGTGAGACTCCATCTCAAAAAAATAAAATAATGAAGT TACCAGTGCACTCCAGCCTGGGCGACAGAGTG_GACTCCATCTCAAAAAAATAAAATAATGAAGT CT C DESI1 Ensembl:ENSG00000100418 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1569063668 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_26499006 RMVar_hsa_circ_100552,RMVar_hsa_circ_108119,RMVar_hsa_circ_110812,RMVar_hsa_circ_214696,RMVar_hsa_circ_214697,RMVar_hsa_circ_214698 5289 RMVar_ID_5289 Human_SNP_ID_704582224 A-to-I Human chr22 - 41599595 41599595 41599595 AGATCGTACCAGTGCACTCCAGCCTGGGCGACAGAGTGAGACTCCATCTCAAAAAAATAAAATAA AGATCGTACCAGTGCACTCCAGCCTGGGCGACGGAGTGAGACTCCATCTCAAAAAAATAAAATAA T C DESI1 Ensembl:ENSG00000100418 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1569063672 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22725464,Human_RBP_ID_26499006 RMVar_hsa_circ_100552,RMVar_hsa_circ_108119,RMVar_hsa_circ_110812,RMVar_hsa_circ_214696,RMVar_hsa_circ_214697,RMVar_hsa_circ_214698 5290 RMVar_ID_5290 Human_SNP_ID_704582237 A-to-I Human chr22 - 41599632 41599632 41599632 TCGCTTGAACCCGGGAGGCAGAGATTGCGATGAGCCGAGATCGTACCAGTGCACTCCAGCCTGGG TCGCTTGAACCCGGGAGGCAGAGATTGCGATGGGCCGAGATCGTACCAGTGCACTCCAGCCTGGG T C DESI1 Ensembl:ENSG00000100418 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1178576047 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14507722,Human_RBP_ID_22725464,Human_RBP_ID_26500406 RMVar_hsa_circ_100552,RMVar_hsa_circ_108119,RMVar_hsa_circ_110812,RMVar_hsa_circ_214696,RMVar_hsa_circ_214697,RMVar_hsa_circ_214698 5291 RMVar_ID_5291 Human_SNP_ID_704582246 A-to-I Human chr22 - 41599656 41599656 41599656 ACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGGGAGGCAGAGATTGCGATGAGCCGAGAT ACTCGGGAGGCTGAGGCAGGAGAATCGCTTGATCCCGGGAGGCAGAGATTGCGATGAGCCGAGAT T A DESI1 Ensembl:ENSG00000100418 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs988001023 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100552,RMVar_hsa_circ_108119,RMVar_hsa_circ_110812,RMVar_hsa_circ_214696,RMVar_hsa_circ_214697,RMVar_hsa_circ_214698 5292 RMVar_ID_5292 Human_SNP_ID_704582259 A-to-I Human chr22 - 41599692 41599692 41599692 AGCCGGGCATGGTGGCGCATGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCT AGCCGGGCATGGTGGCGCATGCCTGTAGTCCCCGCTACTCGGGAGGCTGAGGCAGGAGAATCGCT T G DESI1 Ensembl:ENSG00000100418 Protein coding 3'UTR GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs898587357 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100552,RMVar_hsa_circ_108119,RMVar_hsa_circ_110812,RMVar_hsa_circ_214696,RMVar_hsa_circ_214697,RMVar_hsa_circ_214698 5293 RMVar_ID_5293 Human_SNP_ID_704582262 A-to-I Human chr22 - 41599698 41599698 41599698 AAAATTAGCCGGGCATGGTGGCGCATGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTAGCCGGGCATGGTGGCGCATGCCTGTTGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA T A DESI1 Ensembl:ENSG00000100418 Protein coding 3'UTR GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1569063737 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100552,RMVar_hsa_circ_108119,RMVar_hsa_circ_110812,RMVar_hsa_circ_214696,RMVar_hsa_circ_214697,RMVar_hsa_circ_214698 5294 RMVar_ID_5294 Human_SNP_ID_704582270 A-to-I Human chr22 - 41599716 41599716 41599716 CGTCTCTACTAAAAATACAAAATTAGCCGGGCATGGTGGCGCATGCCTGTAGTCCCAGCTACTCG CGTCTCTACTAAAAATACAAAATTAGCCGGGCGTGGTGGCGCATGCCTGTAGTCCCAGCTACTCG T C DESI1 Ensembl:ENSG00000100418 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1432998659 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100552,RMVar_hsa_circ_108119,RMVar_hsa_circ_110812,RMVar_hsa_circ_214696,RMVar_hsa_circ_214697,RMVar_hsa_circ_214698 5295 RMVar_ID_5295 Human_SNP_ID_704582301 A-to-I Human chr22 - 41599832 41599832 41599832 ATGTGAGGCCTGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGCAG ATGTGAGGCCTGGCGCGGTGGCTCACGCCTGTTATCCCAGCACTTTGGGAGGCCGAGGCAGGCAG T A DESI1 Ensembl:ENSG00000100418 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1185994725 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100552,RMVar_hsa_circ_108119,RMVar_hsa_circ_110812,RMVar_hsa_circ_214696,RMVar_hsa_circ_214697,RMVar_hsa_circ_214698 5296 RMVar_ID_5296 Human_SNP_ID_704582316 A-to-I Human chr22 - 41599868 41599868 41599868 TGGCCAGAAAATACCTTTGATATGGAAAGAATAATGATGTGAGGCCTGGCGCGGTGGCTCACGCC TGGCCAGAAAATACCTTTGATATGGAAAGAATGATGATGTGAGGCCTGGCGCGGTGGCTCACGCC T C DESI1 Ensembl:ENSG00000100418 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs779831995 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_581621,Human_RBP_ID_23187492 RMVar_hsa_circ_100552,RMVar_hsa_circ_108119,RMVar_hsa_circ_110812,RMVar_hsa_circ_214696,RMVar_hsa_circ_214697,RMVar_hsa_circ_214698 5297 RMVar_ID_5297 Human_SNP_ID_704582333 A-to-I Human chr22 - 41599953 41599953 41599953 GCTGGTCTGGAACTCCTGACCTCGGGTGATCCACCTCCCTTGGCCTCCCAAAGTGCTGGGATTAC GCTGGTCTGGAACTCCTGACCTCGGGTGATCCGCCTCCCTTGGCCTCCCAAAGTGCTGGGATTAC T C DESI1 Ensembl:ENSG00000100418 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1351630077 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22725465,Human_RBP_ID_26789860 RMVar_hsa_circ_100552,RMVar_hsa_circ_108119,RMVar_hsa_circ_110812,RMVar_hsa_circ_214696,RMVar_hsa_circ_214697,RMVar_hsa_circ_214698 5298 RMVar_ID_5298 Human_SNP_ID_704582395 A-to-I Human chr22 - 41600185 41600182 41600185 TCTAAGAAAATACCTTTATTTTAATTATTATTATTTTTTGAGACGGAGTCTCGCTCTACCACCCA TCTAAGAAAATACCTTTATTTTAATTATTATT___TTTTGAGACGGAGTCTCGCTCTACCACCCA AAAT A DESI1 Ensembl:ENSG00000100418 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1411034474 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_7087247,Human_RBP_ID_14507724 RMVar_hsa_circ_100552,RMVar_hsa_circ_108119,RMVar_hsa_circ_110812,RMVar_hsa_circ_214696,RMVar_hsa_circ_214697,RMVar_hsa_circ_214698 5299 RMVar_ID_5299 Human_SNP_ID_704582396 A-to-I Human chr22 - 41600185 41600185 41600185 TCTAAGAAAATACCTTTATTTTAATTATTATTATTTTTTGAGACGGAGTCTCGCTCTACCACCCA TCTAAGAAAATACCTTTATTTTAATTATTATTTTTTTTTGAGACGGAGTCTCGCTCTACCACCCA T A DESI1 Ensembl:ENSG00000100418 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs932920453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7087247,Human_RBP_ID_14507724 RMVar_hsa_circ_100552,RMVar_hsa_circ_108119,RMVar_hsa_circ_110812,RMVar_hsa_circ_214696,RMVar_hsa_circ_214697,RMVar_hsa_circ_214698 5300 RMVar_ID_5300 Human_SNP_ID_704585666 A-to-I Human chr22 - 41613181 41613181 41613181 ATGGAAATGTTCTAGATCTGCACTGTCCAGTAAGTAAACACTAGTCACATGTGGCTATTGAATAC ATGGAAATGTTCTAGATCTGCACTGTCCAGTAGGTAAACACTAGTCACATGTGGCTATTGAATAC T C DESI1 Ensembl:ENSG00000100418 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs3179418 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3674089 RMVar_hsa_circ_108119,RMVar_hsa_circ_214698 5301 RMVar_ID_5301 Human_SNP_ID_704588876 A-to-I Human chr22 + 41624299 41624299 41624299 AGTCTCAGCTGCTTGGGAGGCTGAGGCACGAGAATTGCTTGAACCGGGGAGGCAGAGGCTACAGT AGTCTCAGCTGCTTGGGAGGCTGAGGCACGAGGATTGCTTGAACCGGGGAGGCAGAGGCTACAGT A G XRCC6 Ensembl:ENSG00000196419 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1040455394 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22480209 RMVar_hsa_circ_64805,RMVar_hsa_circ_336045,RMVar_hsa_circ_357356,RMVar_hsa_circ_73353 5302 RMVar_ID_5302 Human_SNP_ID_704588930 A-to-I Human chr22 + 41624429 41624429 41624429 AAAATAGGGGCCGGGCGCGGTGGCTCACCTCTATAATCCCAGTACTTTGGGAGGCCGAGGCAGGT AAAATAGGGGCCGGGCGCGGTGGCTCACCTCTGTAATCCCAGTACTTTGGGAGGCCGAGGCAGGT A G XRCC6 Ensembl:ENSG00000196419 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1250978983 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64805,RMVar_hsa_circ_336045,RMVar_hsa_circ_357356,RMVar_hsa_circ_73353 5303 RMVar_ID_5303 Human_SNP_ID_704589846 A-to-I Human chr22 + 41627037 41627035 41627037 ATCTCAAGTGATCCTCCCGCCTTGGTCTCCCAAAGTGTTGGGATTACAGGCATGAGCCACTGTGC ATCTCAAGTGATCCTCCCGCCTTGGTCTCCC__AGTGTTGGGATTACAGGCATGAGCCACTGTGC CAA C XRCC6 Ensembl:ENSG00000196419 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs954189081 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_64805,RMVar_hsa_circ_336045,RMVar_hsa_circ_357356,RMVar_hsa_circ_73353 5304 RMVar_ID_5304 Human_SNP_ID_704589974 A-to-I Human chr22 + 41627450 41627450 41627450 CTGGGCCAACATGGTAAAACTGCGTCTCTACTAAAAATACAAAATTAGCTGGGAGTGGTGGCGGG CTGGGCCAACATGGTAAAACTGCGTCTCTACTGAAAATACAAAATTAGCTGGGAGTGGTGGCGGG A G XRCC6 Ensembl:ENSG00000196419 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs542510173 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64805,RMVar_hsa_circ_336045,RMVar_hsa_circ_357356,RMVar_hsa_circ_73353 5305 RMVar_ID_5305 Human_SNP_ID_704589996 A-to-I Human chr22 + 41627500 41627500 41627500 GGGAGTGGTGGCGGGCGTCTATAATCCCAGCTAGTTGGGAGGCTGAGGCAGGAGAATCGCTTGAA GGGAGTGGTGGCGGGCGTCTATAATCCCAGCTGGTTGGGAGGCTGAGGCAGGAGAATCGCTTGAA A G XRCC6 Ensembl:ENSG00000196419 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1311308553 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64805,RMVar_hsa_circ_336045,RMVar_hsa_circ_357356,RMVar_hsa_circ_73353 5306 RMVar_ID_5306 Human_SNP_ID_704590813 A-to-I Human chr22 + 41630123 41630123 41630123 CTCCTGCCTCAGCCTCCCGAGTAGGTGAGATTACAGGCACGTGTCACCATGCCCAGCTAATTTTT CTCCTGCCTCAGCCTCCCGAGTAGGTGAGATTGCAGGCACGTGTCACCATGCCCAGCTAATTTTT A G XRCC6 Ensembl:ENSG00000196419 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1033037259 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75351,RMVar_hsa_circ_64805,RMVar_hsa_circ_336045,RMVar_hsa_circ_73353,RMVar_hsa_circ_282945,RMVar_hsa_circ_315492,RMVar_hsa_circ_117917,RMVar_hsa_circ_214701 5307 RMVar_ID_5307 Human_SNP_ID_704591439 A-to-I Human chr22 + 41631813 41631813 41631813 GGGAGGTGGAGGTTGTAGCAAGCCGAGATCACACCACTGTACTCCAGCCTGGGCACCATTGAGCA GGGAGGTGGAGGTTGTAGCAAGCCGAGATCACGCCACTGTACTCCAGCCTGGGCACCATTGAGCA A G XRCC6 Ensembl:ENSG00000196419 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs370707482 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14508514 RMVar_hsa_circ_75351,RMVar_hsa_circ_64805,RMVar_hsa_circ_336045,RMVar_hsa_circ_73353,RMVar_hsa_circ_282945,RMVar_hsa_circ_315492,RMVar_hsa_circ_117917,RMVar_hsa_circ_214701 5308 RMVar_ID_5308 Human_SNP_ID_704591742 A-to-I Human chr22 + 41632696 41632696 41632696 AAAAAAAGAATAAGCTGGGTGTGGTGGTGTGCACTTGTAGTCCCAGCTACTCAGGAGGCCGGGGT AAAAAAAGAATAAGCTGGGTGTGGTGGTGTGCTCTTGTAGTCCCAGCTACTCAGGAGGCCGGGGT A T XRCC6 Ensembl:ENSG00000196419 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1016991901 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75351,RMVar_hsa_circ_64805,RMVar_hsa_circ_336045,RMVar_hsa_circ_73353,RMVar_hsa_circ_282945,RMVar_hsa_circ_315492,RMVar_hsa_circ_117917,RMVar_hsa_circ_214701 5309 RMVar_ID_5309 Human_SNP_ID_704592053 A-to-I Human chr22 + 41633655 41633655 41633655 TGCCCACTTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCACCTGGCCAACCGTG TGCCCACTTCGGCCTCCCAAAGTGCTGGGATTCCAGGCATGAGCCACCGCACCTGGCCAACCGTG A C XRCC6 Ensembl:ENSG00000196419 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1324407307 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75351,RMVar_hsa_circ_64805,RMVar_hsa_circ_336045,RMVar_hsa_circ_73353,RMVar_hsa_circ_282945,RMVar_hsa_circ_315492,RMVar_hsa_circ_117917,RMVar_hsa_circ_214701 5310 RMVar_ID_5310 Human_SNP_ID_704592054 A-to-I Human chr22 + 41633655 41633655 41633655 TGCCCACTTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCACCTGGCCAACCGTG TGCCCACTTCGGCCTCCCAAAGTGCTGGGATTGCAGGCATGAGCCACCGCACCTGGCCAACCGTG A G XRCC6 Ensembl:ENSG00000196419 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1324407307 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75351,RMVar_hsa_circ_64805,RMVar_hsa_circ_336045,RMVar_hsa_circ_73353,RMVar_hsa_circ_282945,RMVar_hsa_circ_315492,RMVar_hsa_circ_117917,RMVar_hsa_circ_214701 5311 RMVar_ID_5311 Human_SNP_ID_704592057 A-to-I Human chr22 + 41633661 41633661 41633661 CTTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCACCTGGCCAACCGTGGACCTC CTTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCACCTGGCCAACCGTGGACCTC A G XRCC6 Ensembl:ENSG00000196419 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs8141447 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25675301 RMVar_hsa_circ_75351,RMVar_hsa_circ_64805,RMVar_hsa_circ_336045,RMVar_hsa_circ_73353,RMVar_hsa_circ_282945,RMVar_hsa_circ_315492,RMVar_hsa_circ_117917,RMVar_hsa_circ_214701 5312 RMVar_ID_5312 Human_SNP_ID_704592264 A-to-I Human chr22 + 41634405 41634405 41634405 TAGAGACATTGTTTTGCCATGTTGCCCAGGCTAGTTTCAAACTTCTGTAGCAATCCTCCTGTGTT TAGAGACATTGTTTTGCCATGTTGCCCAGGCTGGTTTCAAACTTCTGTAGCAATCCTCCTGTGTT A G XRCC6 Ensembl:ENSG00000196419 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs555884617 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14508587 RMVar_hsa_circ_75351,RMVar_hsa_circ_64805,RMVar_hsa_circ_336045,RMVar_hsa_circ_73353,RMVar_hsa_circ_282945,RMVar_hsa_circ_315492,RMVar_hsa_circ_117917,RMVar_hsa_circ_214701 5313 RMVar_ID_5313 Human_SNP_ID_704592365 A-to-I Human chr22 + 41634706 41634706 41634706 AGCTAGGATTACAGGCACGTGCTACCACATCCAACTAATTTTTGTATTTTTAGTAGAGTTGGGGT AGCTAGGATTACAGGCACGTGCTACCACATCCGACTAATTTTTGTATTTTTAGTAGAGTTGGGGT A G XRCC6 Ensembl:ENSG00000196419 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs899920204 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23014080 RMVar_hsa_circ_75351,RMVar_hsa_circ_64805,RMVar_hsa_circ_336045,RMVar_hsa_circ_73353,RMVar_hsa_circ_282945,RMVar_hsa_circ_315492,RMVar_hsa_circ_117917,RMVar_hsa_circ_214701 5314 RMVar_ID_5314 Human_SNP_ID_704593444 A-to-I Human chr22 + 41638574 41638574 41638574 TTGGGATGCCGAGGCGGGTGGATCACAAGTTCAAGAGATTGAGACCATCCTGGCCTACATGGTGA TTGGGATGCCGAGGCGGGTGGATCACAAGTTCGAGAGATTGAGACCATCCTGGCCTACATGGTGA A G XRCC6 Ensembl:ENSG00000196419 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1301259431 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26762421 RMVar_hsa_circ_43901,RMVar_hsa_circ_75351,RMVar_hsa_circ_336045,RMVar_hsa_circ_73353,RMVar_hsa_circ_117917,RMVar_hsa_circ_74063,RMVar_hsa_circ_214701,RMVar_hsa_circ_51161,RMVar_hsa_circ_109143,RMVar_hsa_circ_99012,RMVar_hsa_circ_123630,RMVar_hsa_circ_214703,RMVar_hsa_circ_214704,RMVar_hsa_circ_33548,RMVar_hsa_circ_34399,RMVar_hsa_circ_214705 5315 RMVar_ID_5315 Human_SNP_ID_704594816 A-to-I Human chr22 + 41643302 41643302 41643302 TTGGTGGTGGGCGCCTGTAGTCCCAGCTACTCAGGTGACTGAGGCAGGAGAATCACTTGAACCCG TTGGTGGTGGGCGCCTGTAGTCCCAGCTACTCGGGTGACTGAGGCAGGAGAATCACTTGAACCCG A G XRCC6 Ensembl:ENSG00000196419 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1285242330 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43901,RMVar_hsa_circ_75351,RMVar_hsa_circ_336045,RMVar_hsa_circ_73353,RMVar_hsa_circ_117917,RMVar_hsa_circ_74063,RMVar_hsa_circ_214701,RMVar_hsa_circ_51161,RMVar_hsa_circ_109143,RMVar_hsa_circ_99012,RMVar_hsa_circ_123630,RMVar_hsa_circ_214703,RMVar_hsa_circ_214704,RMVar_hsa_circ_33548,RMVar_hsa_circ_34399,RMVar_hsa_circ_214705 5316 RMVar_ID_5316 Human_SNP_ID_704595627 A-to-I Human chr22 + 41646156 41646156 41646156 AAACACCGTCTCTACTAAAATAAAAAGAAATTAGCTGGGTGTCGTGGCAGGTGCCTGTAATCCCA AAACACCGTCTCTACTAAAATAAAAAGAAATTCGCTGGGTGTCGTGGCAGGTGCCTGTAATCCCA A C XRCC6 Ensembl:ENSG00000196419 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs975296128 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43901,RMVar_hsa_circ_75351,RMVar_hsa_circ_336045,RMVar_hsa_circ_73353,RMVar_hsa_circ_117917,RMVar_hsa_circ_74063,RMVar_hsa_circ_214701,RMVar_hsa_circ_51161,RMVar_hsa_circ_109143,RMVar_hsa_circ_99012,RMVar_hsa_circ_123630,RMVar_hsa_circ_214703,RMVar_hsa_circ_214704,RMVar_hsa_circ_33548,RMVar_hsa_circ_34399,RMVar_hsa_circ_214705 5317 RMVar_ID_5317 Human_SNP_ID_704595930 A-to-I Human chr22 + 41647216 41647216 41647216 GACCTCCTGGACTCAAGCGATCCTTCTGTCTCAGCCTCCCAAGTAGCTGGGATCACAGGCATGTG GACCTCCTGGACTCAAGCGATCCTTCTGTCTCGGCCTCCCAAGTAGCTGGGATCACAGGCATGTG A G XRCC6 Ensembl:ENSG00000196419 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1003420807 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43901,RMVar_hsa_circ_336045,RMVar_hsa_circ_73353,RMVar_hsa_circ_117917,RMVar_hsa_circ_214701,RMVar_hsa_circ_51161,RMVar_hsa_circ_109143,RMVar_hsa_circ_99012,RMVar_hsa_circ_123630,RMVar_hsa_circ_214703,RMVar_hsa_circ_214704,RMVar_hsa_circ_33548,RMVar_hsa_circ_321706,RMVar_hsa_circ_214705 5318 RMVar_ID_5318 Human_SNP_ID_704596096 A-to-I Human chr22 + 41647753 41647753 41647753 GTTTTTTTGTTTCGTTTTGTTTTGTTTTGTTTAATAGAGATGAGGTCTCACTATGTTGCTCAGGC GTTTTTTTGTTTCGTTTTGTTTTGTTTTGTTTGATAGAGATGAGGTCTCACTATGTTGCTCAGGC A G XRCC6 Ensembl:ENSG00000196419 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1387973743 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17572845 RMVar_hsa_circ_43901,RMVar_hsa_circ_336045,RMVar_hsa_circ_73353,RMVar_hsa_circ_117917,RMVar_hsa_circ_214701,RMVar_hsa_circ_51161,RMVar_hsa_circ_109143,RMVar_hsa_circ_99012,RMVar_hsa_circ_123630,RMVar_hsa_circ_214703,RMVar_hsa_circ_214704,RMVar_hsa_circ_33548,RMVar_hsa_circ_321706,RMVar_hsa_circ_214705 5319 RMVar_ID_5319 Human_SNP_ID_704596464 A-to-I Human chr22 + 41649053 41649053 41649053 ACCCAGGAGTTTGAGATCAGCCTGGGCATCATAGCGAGACCCTGTCTCTACTAAAAAACTAAAAA ACCCAGGAGTTTGAGATCAGCCTGGGCATCATTGCGAGACCCTGTCTCTACTAAAAAACTAAAAA A T XRCC6 Ensembl:ENSG00000196419 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs150008437 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43901,RMVar_hsa_circ_336045,RMVar_hsa_circ_73353,RMVar_hsa_circ_117917,RMVar_hsa_circ_214701,RMVar_hsa_circ_51161,RMVar_hsa_circ_109143,RMVar_hsa_circ_99012,RMVar_hsa_circ_123630,RMVar_hsa_circ_214703,RMVar_hsa_circ_214704,RMVar_hsa_circ_33548,RMVar_hsa_circ_321706,RMVar_hsa_circ_214705 5320 RMVar_ID_5320 Human_SNP_ID_704596705 A-to-I Human chr22 + 41649284 41649284 41649284 AACCTCTTGGGTTCAGTTGATCCTCCCACCTCAGCCACCTGGGTAGCTGGGACTACAGGCTCATG AACCTCTTGGGTTCAGTTGATCCTCCCACCTCGGCCACCTGGGTAGCTGGGACTACAGGCTCATG A G XRCC6 Ensembl:ENSG00000196419 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1317914135 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43901,RMVar_hsa_circ_336045,RMVar_hsa_circ_73353,RMVar_hsa_circ_117917,RMVar_hsa_circ_214701,RMVar_hsa_circ_51161,RMVar_hsa_circ_109143,RMVar_hsa_circ_99012,RMVar_hsa_circ_123630,RMVar_hsa_circ_214703,RMVar_hsa_circ_214704,RMVar_hsa_circ_33548,RMVar_hsa_circ_321706,RMVar_hsa_circ_214705 5321 RMVar_ID_5321 Human_SNP_ID_704596726 A-to-I Human chr22 + 41649376 41649376 41649376 TTTTTTTTTTTTCATAGAGACAGGATCTCACTATGTTACCCAGGCTGGTCTCGAATTCCTGGGCT TTTTTTTTTTTTCATAGAGACAGGATCTCACTTTGTTACCCAGGCTGGTCTCGAATTCCTGGGCT A T XRCC6 Ensembl:ENSG00000196419 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs186969431 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17572846 RMVar_hsa_circ_43901,RMVar_hsa_circ_336045,RMVar_hsa_circ_73353,RMVar_hsa_circ_117917,RMVar_hsa_circ_214701,RMVar_hsa_circ_51161,RMVar_hsa_circ_109143,RMVar_hsa_circ_99012,RMVar_hsa_circ_123630,RMVar_hsa_circ_214703,RMVar_hsa_circ_214704,RMVar_hsa_circ_33548,RMVar_hsa_circ_321706,RMVar_hsa_circ_214705 5322 RMVar_ID_5322 Human_SNP_ID_704596745 A-to-I Human chr22 + 41649441 41649441 41649441 CAAACGATCCAGCTGCCTTGGCCTCACAAAGTATTGGGATTACAGGCATGAGTCAACGTGCCCTG CAAACGATCCAGCTGCCTTGGCCTCACAAAGTGTTGGGATTACAGGCATGAGTCAACGTGCCCTG A G XRCC6 Ensembl:ENSG00000196419 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs986043100 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17572846 RMVar_hsa_circ_43901,RMVar_hsa_circ_336045,RMVar_hsa_circ_73353,RMVar_hsa_circ_117917,RMVar_hsa_circ_214701,RMVar_hsa_circ_51161,RMVar_hsa_circ_109143,RMVar_hsa_circ_99012,RMVar_hsa_circ_123630,RMVar_hsa_circ_214703,RMVar_hsa_circ_214704,RMVar_hsa_circ_33548,RMVar_hsa_circ_321706,RMVar_hsa_circ_214705 5323 RMVar_ID_5323 Human_SNP_ID_704596746 A-to-I Human chr22 + 41649441 41649441 41649441 CAAACGATCCAGCTGCCTTGGCCTCACAAAGTATTGGGATTACAGGCATGAGTCAACGTGCCCTG CAAACGATCCAGCTGCCTTGGCCTCACAAAGTTTTGGGATTACAGGCATGAGTCAACGTGCCCTG A T XRCC6 Ensembl:ENSG00000196419 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs986043100 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17572846 RMVar_hsa_circ_43901,RMVar_hsa_circ_336045,RMVar_hsa_circ_73353,RMVar_hsa_circ_117917,RMVar_hsa_circ_214701,RMVar_hsa_circ_51161,RMVar_hsa_circ_109143,RMVar_hsa_circ_99012,RMVar_hsa_circ_123630,RMVar_hsa_circ_214703,RMVar_hsa_circ_214704,RMVar_hsa_circ_33548,RMVar_hsa_circ_321706,RMVar_hsa_circ_214705 5324 RMVar_ID_5324 Human_SNP_ID_704597504 A-to-I Human chr22 + 41651863 41651863 41651863 TGGAGTGAAGTGGCGCAATCTCGGCTCACTGCAATCTCCGTCCCCTGGGTTCAAGCGAGTCTCCT TGGAGTGAAGTGGCGCAATCTCGGCTCACTGCCATCTCCGTCCCCTGGGTTCAAGCGAGTCTCCT A C XRCC6 Ensembl:ENSG00000196419 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs540773801 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14508994 RMVar_hsa_circ_336045,RMVar_hsa_circ_117917,RMVar_hsa_circ_214701,RMVar_hsa_circ_51161,RMVar_hsa_circ_109143,RMVar_hsa_circ_99012,RMVar_hsa_circ_123630,RMVar_hsa_circ_214703,RMVar_hsa_circ_214704,RMVar_hsa_circ_321706,RMVar_hsa_circ_214705 5325 RMVar_ID_5325 Human_SNP_ID_704597505 A-to-I Human chr22 + 41651863 41651863 41651863 TGGAGTGAAGTGGCGCAATCTCGGCTCACTGCAATCTCCGTCCCCTGGGTTCAAGCGAGTCTCCT TGGAGTGAAGTGGCGCAATCTCGGCTCACTGCGATCTCCGTCCCCTGGGTTCAAGCGAGTCTCCT A G XRCC6 Ensembl:ENSG00000196419 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs540773801 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14508994 RMVar_hsa_circ_336045,RMVar_hsa_circ_117917,RMVar_hsa_circ_214701,RMVar_hsa_circ_51161,RMVar_hsa_circ_109143,RMVar_hsa_circ_99012,RMVar_hsa_circ_123630,RMVar_hsa_circ_214703,RMVar_hsa_circ_214704,RMVar_hsa_circ_321706,RMVar_hsa_circ_214705 5326 RMVar_ID_5326 Human_SNP_ID_704597661 A-to-I Human chr22 + 41652389 41652382 41652390 ATAATTTGCTTTTTTTTTTTTTTTCTGGAGACAGTGTCTCACTCTGTCACCCAGGCTAGAGTCCA ATAATTTGCTTTTTTTTTTTTTTTCT________TGTCTCACTCTGTCACCCAGGCTAGAGTCCA TGGAGACAG T XRCC6 Ensembl:ENSG00000196419 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1555907190 Functional Loss DEL dbSNP153 27..34 33 - - - Human_RBP_ID_14509015 RMVar_hsa_circ_336045,RMVar_hsa_circ_117917,RMVar_hsa_circ_214701,RMVar_hsa_circ_51161,RMVar_hsa_circ_109143,RMVar_hsa_circ_99012,RMVar_hsa_circ_123630,RMVar_hsa_circ_214703,RMVar_hsa_circ_214704,RMVar_hsa_circ_321706,RMVar_hsa_circ_214705 5327 RMVar_ID_5327 Human_SNP_ID_704597788 A-to-I Human chr22 + 41652839 41652839 41652839 GGGACTACAGGCGTGCACTACCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTTA GGGACTACAGGCGTGCACTACCATGCCCAGCTGATTTTTGTATTTTTAGTAGAGATGGGGTTTTA A G XRCC6 Ensembl:ENSG00000196419 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1278654069 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_336045,RMVar_hsa_circ_117917,RMVar_hsa_circ_214701,RMVar_hsa_circ_51161,RMVar_hsa_circ_109143,RMVar_hsa_circ_99012,RMVar_hsa_circ_123630,RMVar_hsa_circ_214703,RMVar_hsa_circ_214704,RMVar_hsa_circ_321706,RMVar_hsa_circ_214705 5328 RMVar_ID_5328 Human_SNP_ID_704597894 A-to-I Human chr22 + 41653297 41653297 41653297 GTGGTGGTGTGTGACTGTAGTCCCAGCTATTCAGGAAGCAGAAGTGGGAAGATTGCTTGAGCTTG GTGGTGGTGTGTGACTGTAGTCCCAGCTATTCGGGAAGCAGAAGTGGGAAGATTGCTTGAGCTTG A G XRCC6 Ensembl:ENSG00000196419 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs945218128 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_336045,RMVar_hsa_circ_117917,RMVar_hsa_circ_214701,RMVar_hsa_circ_51161,RMVar_hsa_circ_109143,RMVar_hsa_circ_99012,RMVar_hsa_circ_123630,RMVar_hsa_circ_214703,RMVar_hsa_circ_214704,RMVar_hsa_circ_321706,RMVar_hsa_circ_214705 5329 RMVar_ID_5329 Human_SNP_ID_704601905 A-to-I Human chr22 - 41668044 41668044 41668044 TTCTCTACTAGGAATACAAAAATTGGCTGGGCATGGTGGCACATGCCTGTAATCCCAGCTACGTA TTCTCTACTAGGAATACAAAAATTGGCTGGGCGTGGTGGCACATGCCTGTAATCCCAGCTACGTA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1181589864 Functional Loss SNV dbSNP153 33..33 33 - - - 5330 RMVar_ID_5330 Human_SNP_ID_704604000 A-to-I Human chr22 - 41675559 41675559 41675559 AAATTAGCTAAACACAGTGGCACGTGCCTGTAATCCCAGCTGCTTGGGAGACTGAGGCAGGAGAA AAATTAGCTAAACACAGTGGCACGTGCCTGTATTCCCAGCTGCTTGGGAGACTGAGGCAGGAGAA T A SNU13 Ensembl:ENSG00000100138 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs940478449 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85280,RMVar_hsa_circ_94119,RMVar_hsa_circ_214711,RMVar_hsa_circ_80412,RMVar_hsa_circ_214712,RMVar_hsa_circ_214710 5331 RMVar_ID_5331 Human_SNP_ID_704604436 A-to-I Human chr22 - 41677290 41677290 41677290 CAAACTCTGAGTTCAAACAATCTACCTGCCTCAGCCTCCCAGTGGGCTGGGATTACAGGTGTGAG CAAACTCTGAGTTCAAACAATCTACCTGCCTCGGCCTCCCAGTGGGCTGGGATTACAGGTGTGAG T C SNU13 Ensembl:ENSG00000100138 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355951016 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85280,RMVar_hsa_circ_94119,RMVar_hsa_circ_214711,RMVar_hsa_circ_80412,RMVar_hsa_circ_214712,RMVar_hsa_circ_214710 5332 RMVar_ID_5332 Human_SNP_ID_704604448 A-to-I Human chr22 - 41677341 41677341 41677341 TTTTATATTTTTAGTAGAGATGGGGTTTTGCCATGTTGCCCAGGCTGGTCTCAAACTCTGAGTTC TTTTATATTTTTAGTAGAGATGGGGTTTTGCCGTGTTGCCCAGGCTGGTCTCAAACTCTGAGTTC T C SNU13 Ensembl:ENSG00000100138 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs990843008 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85280,RMVar_hsa_circ_94119,RMVar_hsa_circ_214711,RMVar_hsa_circ_80412,RMVar_hsa_circ_214712,RMVar_hsa_circ_214710 5333 RMVar_ID_5333 Human_SNP_ID_704604459 A-to-I Human chr22 - 41677403 41677403 41677403 CTCCCACCTCAGCGTCCCAGGTAGCTGGAACTACAGGTGTACGCCACCACACCTGGCTAATTTTT CTCCCACCTCAGCGTCCCAGGTAGCTGGAACTGCAGGTGTACGCCACCACACCTGGCTAATTTTT T C SNU13 Ensembl:ENSG00000100138 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs908118696 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85280,RMVar_hsa_circ_94119,RMVar_hsa_circ_214711,RMVar_hsa_circ_80412,RMVar_hsa_circ_214712,RMVar_hsa_circ_214710 5334 RMVar_ID_5334 Human_SNP_ID_704604479 A-to-I Human chr22 - 41677475 41677475 41677475 GCAGCCCAGGCTGGAGTGCATTGGCATTGATCATGGCTCACTGCAGCCACGACCTCCTGGGCTTA GCAGCCCAGGCTGGAGTGCATTGGCATTGATCGTGGCTCACTGCAGCCACGACCTCCTGGGCTTA T C SNU13 Ensembl:ENSG00000100138 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs892919294 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85280,RMVar_hsa_circ_94119,RMVar_hsa_circ_214711,RMVar_hsa_circ_80412,RMVar_hsa_circ_214712,RMVar_hsa_circ_214710 5335 RMVar_ID_5335 Human_SNP_ID_704604965 A-to-I Human chr22 - 41679331 41679331 41679331 TCTGGTCTCGAACTCCTGATCTCAGGTGATCTACCTGCCTTGGCCTCCCAAAGTGCTGCTGGGAT TCTGGTCTCGAACTCCTGATCTCAGGTGATCTGCCTGCCTTGGCCTCCCAAAGTGCTGCTGGGAT T C SNU13 Ensembl:ENSG00000100138 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs187625303 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14509357 RMVar_hsa_circ_85280,RMVar_hsa_circ_94119,RMVar_hsa_circ_214711,RMVar_hsa_circ_80412,RMVar_hsa_circ_214712,RMVar_hsa_circ_214710 5336 RMVar_ID_5336 Human_SNP_ID_704604966 A-to-I Human chr22 - 41679331 41679331 41679331 TCTGGTCTCGAACTCCTGATCTCAGGTGATCTACCTGCCTTGGCCTCCCAAAGTGCTGCTGGGAT TCTGGTCTCGAACTCCTGATCTCAGGTGATCTCCCTGCCTTGGCCTCCCAAAGTGCTGCTGGGAT T G SNU13 Ensembl:ENSG00000100138 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs187625303 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14509357 RMVar_hsa_circ_85280,RMVar_hsa_circ_94119,RMVar_hsa_circ_214711,RMVar_hsa_circ_80412,RMVar_hsa_circ_214712,RMVar_hsa_circ_214710 5337 RMVar_ID_5337 Human_SNP_ID_704606068 A-to-I Human chr22 - 41683054 41683054 41683054 AGGAGGTTGCAGTGAGCCAAGATGCCACCACTACACTCCAGCCTGGGTGACAGAGCGAGACCCTG AGGAGGTTGCAGTGAGCCAAGATGCCACCACTGCACTCCAGCCTGGGTGACAGAGCGAGACCCTG T C SNU13 Ensembl:ENSG00000100138 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs367850248 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85280,RMVar_hsa_circ_214710 5338 RMVar_ID_5338 Human_SNP_ID_704606506 A-to-I Human chr22 - 41684972 41684972 41684972 TTTGTATTCTTAGTAGAGACGGGGGTTTCACCATGTCATCCAGGCTGGTCTTGAACTCCTGACCT TTTGTATTCTTAGTAGAGACGGGGGTTTCACCGTGTCATCCAGGCTGGTCTTGAACTCCTGACCT T C SNU13 Ensembl:ENSG00000100138 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs759076709 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85280,RMVar_hsa_circ_214710 5339 RMVar_ID_5339 Human_SNP_ID_704606513 A-to-I Human chr22 - 41684999 41684999 41684999 GGTGCCTGCCACCACACCCAGATAATTTTTGTATTCTTAGTAGAGACGGGGGTTTCACCATGTCA GGTGCCTGCCACCACACCCAGATAATTTTTGTGTTCTTAGTAGAGACGGGGGTTTCACCATGTCA T C SNU13 Ensembl:ENSG00000100138 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1014431572 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85280,RMVar_hsa_circ_214710 5340 RMVar_ID_5340 Human_SNP_ID_704606518 A-to-I Human chr22 - 41685012 41685012 41685012 AGCTGGGATTACAGGTGCCTGCCACCACACCCAGATAATTTTTGTATTCTTAGTAGAGACGGGGG AGCTGGGATTACAGGTGCCTGCCACCACACCCGGATAATTTTTGTATTCTTAGTAGAGACGGGGG T C SNU13 Ensembl:ENSG00000100138 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1005436280 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85280,RMVar_hsa_circ_214710 5341 RMVar_ID_5341 Human_SNP_ID_704606958 A-to-I Human chr22 - 41686586 41686586 41686586 TCAAATAAAACATTTGTATGGCCGGACGTGGTAGCTCACACCTGTAATCCCAGCACTTTGGGAGG TCAAATAAAACATTTGTATGGCCGGACGTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGG T C SNU13 Ensembl:ENSG00000100138 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1236035140 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85280,RMVar_hsa_circ_214710 5342 RMVar_ID_5342 Human_SNP_ID_704607143 A-to-I Human chr22 - 41687158 41687158 41687158 GGTCCGGAGTTTGAGACCAGCCTGGCCAACATAGTGAAACCCTGTTTCTACTAAAAATTCAAAAA GGTCCGGAGTTTGAGACCAGCCTGGCCAACATGGTGAAACCCTGTTTCTACTAAAAATTCAAAAA T C SNU13 Ensembl:ENSG00000100138 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1320253575 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85280,RMVar_hsa_circ_214710 5343 RMVar_ID_5343 Human_SNP_ID_704626675 A-to-I Human chr22 + 41756613 41756613 41756613 CTCCTGCGTCAGCTTCCTGAGTAGCTAGGACTACAGGCACTTGCCACCACGCTTGTCTAATTTTT CTCCTGCGTCAGCTTCCTGAGTAGCTAGGACTGCAGGCACTTGCCACCACGCTTGTCTAATTTTT A G MEI1 Ensembl:ENSG00000167077 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1016803293 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70875 5344 RMVar_ID_5344 Human_SNP_ID_704627004 A-to-I Human chr22 + 41757928 41757928 41757928 CAGGAGTTTGAGACCAGCCTGGCCAACATGGCAAAACCCTGCCTCTACTAAAAATACAAAAAATT CAGGAGTTTGAGACCAGCCTGGCCAACATGGCCAAACCCTGCCTCTACTAAAAATACAAAAAATT A C MEI1 Ensembl:ENSG00000167077 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1262958906 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70875 5345 RMVar_ID_5345 Human_SNP_ID_704635961 A-to-I Human chr22 + 41791316 41791316 41791316 CCAGACCAGCCTGGGCAACACAGCACAACCCTATCTCTATAAAAAATACAAAAAATTAGCTGGAC CCAGACCAGCCTGGGCAACACAGCACAACCCTCTCTCTATAAAAAATACAAAAAATTAGCTGGAC A C MEI1 Ensembl:ENSG00000167077 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1413220339 Functional Loss SNV dbSNP153 33..33 33 - - - 5346 RMVar_ID_5346 Human_SNP_ID_704635962 A-to-I Human chr22 + 41791316 41791316 41791316 CCAGACCAGCCTGGGCAACACAGCACAACCCTATCTCTATAAAAAATACAAAAAATTAGCTGGAC CCAGACCAGCCTGGGCAACACAGCACAACCCTGTCTCTATAAAAAATACAAAAAATTAGCTGGAC A G MEI1 Ensembl:ENSG00000167077 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1413220339 Functional Loss SNV dbSNP153 33..33 33 - - - 5347 RMVar_ID_5347 Human_SNP_ID_704635973 A-to-I Human chr22 + 41791341 41791341 41791341 CAACCCTATCTCTATAAAAAATACAAAAAATTAGCTGGACGTGGTGGCACATGCCTGTAGTTCCA CAACCCTATCTCTATAAAAAATACAAAAAATTGGCTGGACGTGGTGGCACATGCCTGTAGTTCCA A G MEI1 Ensembl:ENSG00000167077 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs995854530 Functional Loss SNV dbSNP153 33..33 33 - - - 5348 RMVar_ID_5348 Human_SNP_ID_704637519 A-to-I Human chr22 + 41797544 41797544 41797544 TGAGACAGGAGAACTGCTTGAACTTGGGCGGCAGAGGTTGCAGTCAGCTAAGATTGCACCACTGC TGAGACAGGAGAACTGCTTGAACTTGGGCGGCGGAGGTTGCAGTCAGCTAAGATTGCACCACTGC A G MEI1 Ensembl:ENSG00000167077 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1004524788 Functional Loss SNV dbSNP153 33..33 33 - - - 5349 RMVar_ID_5349 Human_SNP_ID_704641175 A-to-I Human chr22 + 41811533 41811533 41811533 TCACTGCAACCTCTGCCTCCCAGGTTCAAGTGATTCTTGTGCCTCAGCCTCCCGAGTAGCTGGAA TCACTGCAACCTCTGCCTCCCAGGTTCAAGTGGTTCTTGTGCCTCAGCCTCCCGAGTAGCTGGAA A G CCDC134 Ensembl:ENSG00000100147 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs148226160 Functional Loss SNV dbSNP153 33..33 33 - - - 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 5350 RMVar_ID_5350 Human_SNP_ID_704641298 A-to-I Human chr22 + 41812193 41812193 41812193 CCTGTAATCCCAGCACTTTGGGAAGCCGAGGCAGGCGGATTACTTGAGTTCGAGTTTGAGACCAG CCTGTAATCCCAGCACTTTGGGAAGCCGAGGCGGGCGGATTACTTGAGTTCGAGTTTGAGACCAG A G CCDC134 Ensembl:ENSG00000100147 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs993562097 Functional Loss SNV dbSNP153 33..33 33 - - - 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 5351 RMVar_ID_5351 Human_SNP_ID_704641312 A-to-I Human chr22 + 41812256 41812256 41812256 AGCCTGGCCAAACACGGTGAAACCCCATCTCTACCAAAAATATAAAAAAGTAGCCGGGTGTGGTG AGCCTGGCCAAACACGGTGAAACCCCATCTCTGCCAAAAATATAAAAAAGTAGCCGGGTGTGGTG A G CCDC134 Ensembl:ENSG00000100147 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs934337225 Functional Loss SNV dbSNP153 33..33 33 - - - 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 5352 RMVar_ID_5352 Human_SNP_ID_704641415 A-to-I Human chr22 + 41812540 41812540 41812540 TAATTTCAGGCCGAGTGCAGTGGCTCATGCCTATAATCCCAGAGCTTTAGAAGGCCGAGGTAGGA TAATTTCAGGCCGAGTGCAGTGGCTCATGCCTGTAATCCCAGAGCTTTAGAAGGCCGAGGTAGGA A G CCDC134 Ensembl:ENSG00000100147 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1206499868 Functional Loss SNV dbSNP153 33..33 33 - - - 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 5353 RMVar_ID_5353 Human_SNP_ID_704647262 A-to-I Human chr22 + 41835647 41835647 41835647 ACCGTGCCTGGCCGAGCCACCTAATTTTTTTTAGAGACAGTGTCTGGCTGTTGCCCAGGCTGGAG ACCGTGCCTGGCCGAGCCACCTAATTTTTTTTGGAGACAGTGTCTGGCTGTTGCCCAGGCTGGAG A G SREBF2 Ensembl:ENSG00000198911 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs543907830 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10054357,Human_RBP_ID_14510054,Human_RBP_ID_24494476,Human_RBP_ID_27039258 RMVar_hsa_circ_122139,RMVar_hsa_circ_214730,RMVar_hsa_circ_85583,RMVar_hsa_circ_214729 5354 RMVar_ID_5354 Human_SNP_ID_704647315 A-to-I Human chr22 + 41835886 41835886 41835886 GGCACATGCAGTCCTCCTGTCTTGGCCTCCCAAAGTGCTGGGATTACTGGCATGAGCCACTGTAC GGCACATGCAGTCCTCCTGTCTTGGCCTCCCACAGTGCTGGGATTACTGGCATGAGCCACTGTAC A C SREBF2 Ensembl:ENSG00000198911 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1406873290 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122139,RMVar_hsa_circ_214730,RMVar_hsa_circ_85583,RMVar_hsa_circ_214729 5355 RMVar_ID_5355 Human_SNP_ID_704647359 A-to-I Human chr22 + 41836116 41836116 41836116 CCATTTCTCTGTCCTTCCAGAAGACCTGGTTTATAACAGTGCATAAGGCTTTTTCTCAAAATAGT CCATTTCTCTGTCCTTCCAGAAGACCTGGTTTGTAACAGTGCATAAGGCTTTTTCTCAAAATAGT A G SREBF2 Ensembl:ENSG00000198911 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1177779103 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2720565 RMVar_hsa_circ_122139,RMVar_hsa_circ_214730,RMVar_hsa_circ_85583,RMVar_hsa_circ_214729 5356 RMVar_ID_5356 Human_SNP_ID_704647364 A-to-I Human chr22 + 41836146 41836146 41836146 TTATAACAGTGCATAAGGCTTTTTCTCAAAATAGTTATATACCGCACAAGGAAGAGGTGTGGCTG TTATAACAGTGCATAAGGCTTTTTCTCAAAATGGTTATATACCGCACAAGGAAGAGGTGTGGCTG A G SREBF2 Ensembl:ENSG00000198911 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1453981099 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122139,RMVar_hsa_circ_214730,RMVar_hsa_circ_85583,RMVar_hsa_circ_214729 5357 RMVar_ID_5357 Human_SNP_ID_704647898 A-to-I Human chr22 + 41838088 41838087 41838089 TGTTATATATCTCTATTTTGAGAAAGGGCCTCATGTGCCATTACACACCAGGTCTTCTGGAAGGG TGTTATATATCTCTATTTTGAGAAAGGGCCTC__GTGCCATTACACACCAGGTCTTCTGGAAGGG CAT C SREBF2 Ensembl:ENSG00000198911 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs906314667 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_7087882,Human_RBP_ID_14510134 RMVar_hsa_circ_122139,RMVar_hsa_circ_214730,RMVar_hsa_circ_85583,RMVar_hsa_circ_214729 5358 RMVar_ID_5358 Human_SNP_ID_704648988 A-to-I Human chr22 + 41842786 41842786 41842786 CCGAGCCGGGTGAATCATGGGGTCAGGAGATCAAGACCATCCTGGCTAACATGGTGAAACCCTGT CCGAGCCGGGTGAATCATGGGGTCAGGAGATCGAGACCATCCTGGCTAACATGGTGAAACCCTGT A G SREBF2 Ensembl:ENSG00000198911 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1248714255 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122139,RMVar_hsa_circ_214730,RMVar_hsa_circ_85583,RMVar_hsa_circ_214729 5359 RMVar_ID_5359 Human_SNP_ID_704649195 A-to-I Human chr22 + 41843726 41843726 41843726 TGTTTATCAAGAAGTGTCTGTCCAGGCGCAGTAGCTCATACCTGTAATCCTAGCACTTTGGGAGG TGTTTATCAAGAAGTGTCTGTCCAGGCGCAGTGGCTCATACCTGTAATCCTAGCACTTTGGGAGG A G SREBF2 Ensembl:ENSG00000198911 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1060487 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17572850 RMVar_hsa_circ_122139,RMVar_hsa_circ_214730,RMVar_hsa_circ_85583,RMVar_hsa_circ_214729 5360 RMVar_ID_5360 Human_SNP_ID_704649199 A-to-I Human chr22 + 41843739 41843739 41843739 GTGTCTGTCCAGGCGCAGTAGCTCATACCTGTAATCCTAGCACTTTGGGAGGCCAAGATGAGAGG GTGTCTGTCCAGGCGCAGTAGCTCATACCTGTCATCCTAGCACTTTGGGAGGCCAAGATGAGAGG A C SREBF2 Ensembl:ENSG00000198911 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs879808521 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17572850 RMVar_hsa_circ_122139,RMVar_hsa_circ_214730,RMVar_hsa_circ_85583,RMVar_hsa_circ_214729 5361 RMVar_ID_5361 Human_SNP_ID_704649200 A-to-I Human chr22 + 41843739 41843739 41843739 GTGTCTGTCCAGGCGCAGTAGCTCATACCTGTAATCCTAGCACTTTGGGAGGCCAAGATGAGAGG GTGTCTGTCCAGGCGCAGTAGCTCATACCTGTGATCCTAGCACTTTGGGAGGCCAAGATGAGAGG A G SREBF2 Ensembl:ENSG00000198911 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs879808521 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17572850 RMVar_hsa_circ_122139,RMVar_hsa_circ_214730,RMVar_hsa_circ_85583,RMVar_hsa_circ_214729 5362 RMVar_ID_5362 Human_SNP_ID_704650767 A-to-I Human chr22 + 41850019 41850019 41850019 AAAATTAGCCGGGCGTAGTGGCACACACCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCGAGAGA AAAATTAGCCGGGCGTAGTGGCACACACCTGTGGTCCCAGCTACTCGGGAGGCTGAGGCGAGAGA A G SREBF2 Ensembl:ENSG00000198911 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs545461019 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122139,RMVar_hsa_circ_214730,RMVar_hsa_circ_85583,RMVar_hsa_circ_214729 5363 RMVar_ID_5363 Human_SNP_ID_704650986 A-to-I Human chr22 + 41850840 41850840 41850840 TTGGCTCACTGCAACCTCTGCCTCCAGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGC TTGGCTCACTGCAACCTCTGCCTCCAGGGTTCCAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGC A C SREBF2 Ensembl:ENSG00000198911 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1431553305 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122139,RMVar_hsa_circ_214730,RMVar_hsa_circ_85583,RMVar_hsa_circ_214729 5364 RMVar_ID_5364 Human_SNP_ID_704651240 A-to-I Human chr22 + 41851678 41851678 41851678 ACCACGCCCAGCTGATTTTTTGTATTTTAAGTAGAGAGAGGGTTTCACCCTGTTGGCCAGGCTGA ACCACGCCCAGCTGATTTTTTGTATTTTAAGTCGAGAGAGGGTTTCACCCTGTTGGCCAGGCTGA A C SREBF2 Ensembl:ENSG00000198911 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs544861589 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122139,RMVar_hsa_circ_214730,RMVar_hsa_circ_85583,RMVar_hsa_circ_214729 5365 RMVar_ID_5365 Human_SNP_ID_704651248 A-to-I Human chr22 + 41851704 41851704 41851704 TTAAGTAGAGAGAGGGTTTCACCCTGTTGGCCAGGCTGATCTTGAACTCCTGACTGCAGGTGATC TTAAGTAGAGAGAGGGTTTCACCCTGTTGGCCTGGCTGATCTTGAACTCCTGACTGCAGGTGATC A T SREBF2 Ensembl:ENSG00000198911 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1028247933 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17572854 RMVar_hsa_circ_122139,RMVar_hsa_circ_214730,RMVar_hsa_circ_85583,RMVar_hsa_circ_214729 5366 RMVar_ID_5366 Human_SNP_ID_704652066 A-to-I Human chr22 + 41854423 41854423 41854423 ACCTCAGGTGATCCACCCGCCTCGGCCTCCCAAAGTGCTGAGATTGCAGGGGTGAACCACCATGC ACCTCAGGTGATCCACCCGCCTCGGCCTCCCACAGTGCTGAGATTGCAGGGGTGAACCACCATGC A C SREBF2 Ensembl:ENSG00000198911 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs955634445 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122139,RMVar_hsa_circ_214730,RMVar_hsa_circ_85583,RMVar_hsa_circ_214729 5367 RMVar_ID_5367 Human_SNP_ID_704652108 A-to-I Human chr22 + 41854611 41854611 41854611 TATTTAGAATCCGGGGGTGGTGGCTCATTCCTATAATCCCAGCACTTTGGGAGGCTGAGGCGGGC TATTTAGAATCCGGGGGTGGTGGCTCATTCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGC A G SREBF2 Ensembl:ENSG00000198911 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs996943083 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122139,RMVar_hsa_circ_214730,RMVar_hsa_circ_85583,RMVar_hsa_circ_214729 5368 RMVar_ID_5368 Human_SNP_ID_704652144 A-to-I Human chr22 + 41854771 41854770 41854771 CGTGCCTGTAATGCCAGCTACTCAGGAGCCTGAGGCTTGAGAATTGCTTGAACGTGGGAGGCGGA CGTGCCTGTAATGCCAGCTACTCAGGAGCCTG_GGCTTGAGAATTGCTTGAACGTGGGAGGCGGA GA G SREBF2 Ensembl:ENSG00000198911 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355921244 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_8551697,Human_RBP_ID_14510647 RMVar_hsa_circ_122139,RMVar_hsa_circ_214730,RMVar_hsa_circ_85583,RMVar_hsa_circ_214729 5369 RMVar_ID_5369 Human_SNP_ID_704652145 A-to-I Human chr22 + 41854771 41854771 41854771 CGTGCCTGTAATGCCAGCTACTCAGGAGCCTGAGGCTTGAGAATTGCTTGAACGTGGGAGGCGGA CGTGCCTGTAATGCCAGCTACTCAGGAGCCTGTGGCTTGAGAATTGCTTGAACGTGGGAGGCGGA A T SREBF2 Ensembl:ENSG00000198911 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1457487289 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8551697,Human_RBP_ID_14510647 RMVar_hsa_circ_122139,RMVar_hsa_circ_214730,RMVar_hsa_circ_85583,RMVar_hsa_circ_214729 5370 RMVar_ID_5370 Human_SNP_ID_704652299 A-to-I Human chr22 + 41855370 41855370 41855370 CATGGTTAAATTAAACTTCGTCTACTAAAAATACAAAAATTAGCTGGGTGTGGTGGCGGGCACCT CATGGTTAAATTAAACTTCGTCTACTAAAAATGCAAAAATTAGCTGGGTGTGGTGGCGGGCACCT A G SREBF2 Ensembl:ENSG00000198911 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1044656287 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122139,RMVar_hsa_circ_214730,RMVar_hsa_circ_85583,RMVar_hsa_circ_214729 5371 RMVar_ID_5371 Human_SNP_ID_704652403 A-to-I Human chr22 + 41855778 41855778 41855778 GTAGTATAACTTTTTTTTTTTTTTTTTGAGTCAGGGGTCTTGCTCTGTTGTTCCAGGCTTGAGTA GTAGTATAACTTTTTTTTTTTTTTTTTGAGTCGGGGGTCTTGCTCTGTTGTTCCAGGCTTGAGTA A G SREBF2 Ensembl:ENSG00000198911 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1044601965 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7088017,Human_RBP_ID_14510661 RMVar_hsa_circ_122139,RMVar_hsa_circ_214730,RMVar_hsa_circ_85583,RMVar_hsa_circ_214729 5372 RMVar_ID_5372 Human_SNP_ID_704652410 A-to-I Human chr22 + 41855810 41855810 41855810 AGGGGTCTTGCTCTGTTGTTCCAGGCTTGAGTACAGTGGTACAGTCGTGGCTCACTGCAGCCTTG AGGGGTCTTGCTCTGTTGTTCCAGGCTTGAGTGCAGTGGTACAGTCGTGGCTCACTGCAGCCTTG A G SREBF2 Ensembl:ENSG00000198911 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1398545509 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122139,RMVar_hsa_circ_214730,RMVar_hsa_circ_85583,RMVar_hsa_circ_214729 5373 RMVar_ID_5373 Human_SNP_ID_704652525 A-to-I Human chr22 + 41856266 41856266 41856266 CTCCCACCTCAGCCTGCCGAGTAGCTGGGCCTACAGGTGCGTGCCACCATGCCCCCTGCTAAAGT CTCCCACCTCAGCCTGCCGAGTAGCTGGGCCTGCAGGTGCGTGCCACCATGCCCCCTGCTAAAGT A G SREBF2 Ensembl:ENSG00000198911 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1050507543 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122139,RMVar_hsa_circ_214730,RMVar_hsa_circ_85583,RMVar_hsa_circ_214729 5374 RMVar_ID_5374 Human_SNP_ID_704652546 A-to-I Human chr22 + 41856338 41856338 41856338 TTTTGTAGAGATGGAGTCTCGCTATGTTGCCCAAGCTGGTCTCAAACTCCTGAACTTGAGCGATC TTTTGTAGAGATGGAGTCTCGCTATGTTGCCCCAGCTGGTCTCAAACTCCTGAACTTGAGCGATC A C SREBF2 Ensembl:ENSG00000198911 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs969082284 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122139,RMVar_hsa_circ_214730,RMVar_hsa_circ_85583,RMVar_hsa_circ_214729 5375 RMVar_ID_5375 Human_SNP_ID_704652554 A-to-I Human chr22 + 41856381 41856372 41856381 AAACTCCTGAACTTGAGCGATCTGGCCACCTCAGCCTCTCAAAGTGCTGGGATTACAGGCATGTG AAACTCCTGAACTTGAGCGATCTG_________GCCTCTCAAAGTGCTGGGATTACAGGCATGTG GGCCACCTCA G SREBF2 Ensembl:ENSG00000198911 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs960467579 Functional Loss DEL dbSNP153 25..33 33 - - - RMVar_hsa_circ_122139,RMVar_hsa_circ_214730,RMVar_hsa_circ_85583,RMVar_hsa_circ_214729 5376 RMVar_ID_5376 Human_SNP_ID_704652557 A-to-I Human chr22 + 41856376 41856376 41856376 GTCTCAAACTCCTGAACTTGAGCGATCTGGCCACCTCAGCCTCTCAAAGTGCTGGGATTACAGGC GTCTCAAACTCCTGAACTTGAGCGATCTGGCCCCCTCAGCCTCTCAAAGTGCTGGGATTACAGGC A C SREBF2 Ensembl:ENSG00000198911 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1201541228 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122139,RMVar_hsa_circ_214730,RMVar_hsa_circ_85583,RMVar_hsa_circ_214729 5377 RMVar_ID_5377 Human_SNP_ID_704652650 A-to-I Human chr22 + 41856873 41856873 41856873 GAGGCAGGTGGATCACCTAAGGTCAGGAGTTCAAGACCAGCCTGGCCAACACGAAGTCTCTACTA GAGGCAGGTGGATCACCTAAGGTCAGGAGTTCCAGACCAGCCTGGCCAACACGAAGTCTCTACTA A C SREBF2 Ensembl:ENSG00000198911 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1223572036 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122139,RMVar_hsa_circ_214730,RMVar_hsa_circ_85583,RMVar_hsa_circ_214729 5378 RMVar_ID_5378 Human_SNP_ID_704652682 A-to-I Human chr22 + 41856973 41856973 41856973 GCTGTAATCCCGGCTACATGGGAGGCTGAGACAGGAGAGTTGCTTGAACCTGGGAGACAGAAGTT GCTGTAATCCCGGCTACATGGGAGGCTGAGACCGGAGAGTTGCTTGAACCTGGGAGACAGAAGTT A C SREBF2 Ensembl:ENSG00000198911 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1269210629 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122139,RMVar_hsa_circ_214730,RMVar_hsa_circ_85583,RMVar_hsa_circ_214729 5379 RMVar_ID_5379 Human_SNP_ID_704653420 A-to-I Human chr22 + 41859850 41859850 41859850 TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCACCCAGGCTGGAGTGCAGTGGCGCAATCTCGGT TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCAATCTCGGT A G SREBF2 Ensembl:ENSG00000198911 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1212689954 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122139,RMVar_hsa_circ_214730,RMVar_hsa_circ_85583,RMVar_hsa_circ_214729 5380 RMVar_ID_5380 Human_SNP_ID_704653689 A-to-I Human chr22 + 41860867 41860867 41860867 CCACCACTGCCTTCCAGCCTGGGCAAGAGAGCAAGACCCTGTCTCAAAAAAATAAAAAAAAAAGA CCACCACTGCCTTCCAGCCTGGGCAAGAGAGCGAGACCCTGTCTCAAAAAAATAAAAAAAAAAGA A G SREBF2 Ensembl:ENSG00000198911 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1238664587 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122139,RMVar_hsa_circ_214730,RMVar_hsa_circ_85583,RMVar_hsa_circ_214729 5381 RMVar_ID_5381 Human_SNP_ID_704654427 A-to-I Human chr22 + 41863964 41863936 41863964 AGTACAGTGACGCAGTCATCTCGGCTTACTGCAACCTCTGCCTCCTGGGTTCAAGCGATTCTCCT AGTAC____________________________ACCTCTGCCTCCTGGGTTCAAGCGATTCTCCT CAGTGACGCAGTCATCTCGGCTTACTGCA C SREBF2 Ensembl:ENSG00000198911 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs746763239 Functional Loss DEL dbSNP153 6..33 33 - - - RMVar_hsa_circ_122139,RMVar_hsa_circ_214730,RMVar_hsa_circ_85583,RMVar_hsa_circ_214729 5382 RMVar_ID_5382 Human_SNP_ID_704656243 A-to-I Human chr22 + 41869609 41869609 41869609 AGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAAGCACCTGCCACTGCA AGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAAGCACCTGCCACTGCA A G SREBF2 Ensembl:ENSG00000198911 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs968729124 Functional Loss SNV dbSNP153 33..33 33 - - - 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_287927,RMVar_hsa_circ_214729,RMVar_hsa_circ_29319,RMVar_hsa_circ_8651,RMVar_hsa_circ_214732,RMVar_hsa_circ_34127,RMVar_hsa_circ_354754,RMVar_hsa_circ_355447,RMVar_hsa_circ_37548 5383 RMVar_ID_5383 Human_SNP_ID_704658758 A-to-I Human chr22 + 41879122 41879122 41879122 GGCTCAAGTGATCCTCTCACCTTGACGTCCCAAAGTGTTAGGATTACAGGCATGAGCCACCACGC GGCTCAAGTGATCCTCTCACCTTGACGTCCCAGAGTGTTAGGATTACAGGCATGAGCCACCACGC A G SREBF2 Ensembl:ENSG00000198911 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1289222475 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9595,RMVar_hsa_circ_24121,RMVar_hsa_circ_214730,RMVar_hsa_circ_85583,RMVar_hsa_circ_354754,RMVar_hsa_circ_88010,RMVar_hsa_circ_214734,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_214735,RMVar_hsa_circ_302948,RMVar_hsa_circ_368734,RMVar_hsa_circ_214738,RMVar_hsa_circ_214739,RMVar_hsa_circ_106158,RMVar_hsa_circ_214740,RMVar_hsa_circ_214741 5384 RMVar_ID_5384 Human_SNP_ID_704659612 A-to-I Human chr22 + 41882683 41882683 41882683 CAAAAATTAGCCGGGTGTGGTGGCACGTGCCTATAATCCCAGTTACTCGAGAGGCTAAGGCAGGA CAAAAATTAGCCGGGTGTGGTGGCACGTGCCTGTAATCCCAGTTACTCGAGAGGCTAAGGCAGGA A G SREBF2 Ensembl:ENSG00000198911 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs550821668 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24121,RMVar_hsa_circ_214730,RMVar_hsa_circ_85583,RMVar_hsa_circ_354754,RMVar_hsa_circ_88010,RMVar_hsa_circ_214734,RMVar_hsa_circ_214733,RMVar_hsa_circ_125188,RMVar_hsa_circ_335945,RMVar_hsa_circ_348704,RMVar_hsa_circ_354402,RMVar_hsa_circ_45165,RMVar_hsa_circ_214736,RMVar_hsa_circ_214735,RMVar_hsa_circ_368734,RMVar_hsa_circ_214738,RMVar_hsa_circ_214739,RMVar_hsa_circ_295221,RMVar_hsa_circ_214741,RMVar_hsa_circ_344694,RMVar_hsa_circ_214743 5385 RMVar_ID_5385 Human_SNP_ID_704659956 A-to-I Human chr22 + 41884191 41884191 41884191 AGAGTCTCGCTCTGTTGCCCAGGCTGGAGTGCAGTGGTGCGATCTCAGCTCACTGCAACCTCCGC AGAGTCTCGCTCTGTTGCCCAGGCTGGAGTGCGGTGGTGCGATCTCAGCTCACTGCAACCTCCGC A G SREBF2 Ensembl:ENSG00000198911 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1018085079 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24121,RMVar_hsa_circ_214730,RMVar_hsa_circ_85583,RMVar_hsa_circ_354754,RMVar_hsa_circ_88010,RMVar_hsa_circ_214734,RMVar_hsa_circ_214733,RMVar_hsa_circ_125188,RMVar_hsa_circ_335945,RMVar_hsa_circ_348704,RMVar_hsa_circ_354402,RMVar_hsa_circ_45165,RMVar_hsa_circ_214736,RMVar_hsa_circ_214735,RMVar_hsa_circ_368734,RMVar_hsa_circ_214738,RMVar_hsa_circ_214739,RMVar_hsa_circ_295221,RMVar_hsa_circ_214741,RMVar_hsa_circ_344694,RMVar_hsa_circ_214743 5386 RMVar_ID_5386 Human_SNP_ID_704659974 A-to-I Human chr22 + 41884235 41884235 41884235 TCAGCTCACTGCAACCTCCGCATCGCAGGCTCAAGCAATTCTTCTGCCTCAGCCTTCCAAGTAGC TCAGCTCACTGCAACCTCCGCATCGCAGGCTCGAGCAATTCTTCTGCCTCAGCCTTCCAAGTAGC A G SREBF2 Ensembl:ENSG00000198911 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1369900339 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24121,RMVar_hsa_circ_214730,RMVar_hsa_circ_85583,RMVar_hsa_circ_354754,RMVar_hsa_circ_88010,RMVar_hsa_circ_214734,RMVar_hsa_circ_214733,RMVar_hsa_circ_125188,RMVar_hsa_circ_335945,RMVar_hsa_circ_348704,RMVar_hsa_circ_354402,RMVar_hsa_circ_45165,RMVar_hsa_circ_214736,RMVar_hsa_circ_214735,RMVar_hsa_circ_368734,RMVar_hsa_circ_214738,RMVar_hsa_circ_214739,RMVar_hsa_circ_295221,RMVar_hsa_circ_214741,RMVar_hsa_circ_344694,RMVar_hsa_circ_214743 5387 RMVar_ID_5387 Human_SNP_ID_704663046 A-to-I Human chr22 + 41895636 41895636 41895636 TTTTGTACTTTTAGTAGAGATGAGGTTTCACCATGTCATTCAGGCTGGTCTTGAACTCCTGATCT TTTTGTACTTTTAGTAGAGATGAGGTTTCACCGTGTCATTCAGGCTGGTCTTGAACTCCTGATCT A G SREBF2 Ensembl:ENSG00000198911 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs987678378 Functional Loss SNV dbSNP153 33..33 33 - - - 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_70877,RMVar_hsa_circ_92420,RMVar_hsa_circ_214745,RMVar_hsa_circ_285826,RMVar_hsa_circ_214748,RMVar_hsa_circ_22318 5388 RMVar_ID_5388 Human_SNP_ID_704669149 A-to-I Human chr22 - 41916909 41916909 41916909 TTTTTTTTTTTTGTTTGTTTGTTTGTTTTTTTAAGACGGAGTCTCAATCTGTTTCCCAGGCTGGA TTTTTTTTTTTTGTTTGTTTGTTTGTTTTTTTTAGACGGAGTCTCAATCTGTTTCCCAGGCTGGA T A HSALNG0135671 RNACentral:URS0000EA9A62 lincRNA exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1366761802 Functional Loss SNV dbSNP153 33..33 33 - - - 5389 RMVar_ID_5389 Human_SNP_ID_704669654 A-to-I Human chr22 - 41918681 41918681 41918681 GGCATGGTGGCGGGTCCTTATAAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGGTTGAA GGCATGGTGGCGGGTCCTTATAAATCCCAGCTGCTCGGGAGGCTGAGGCAGGAGAATTGGTTGAA T C HSALNG0135671 RNACentral:URS0000EA9A62 lincRNA exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs942289619 Functional Loss SNV dbSNP153 33..33 33 - - - 5390 RMVar_ID_5390 Human_SNP_ID_704669681 A-to-I Human chr22 - 41918790 41918790 41918790 TTGAACCTGGGAGGCGGAGGTTGGAGTGAGCCAAGATCGCGCCACTGGACTCCAGCTGGGCGACA TTGAACCTGGGAGGCGGAGGTTGGAGTGAGCCCAGATCGCGCCACTGGACTCCAGCTGGGCGACA T G HSALNG0135671 RNACentral:URS0000EA9A62 lincRNA exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1233673578 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4701929,Human_RBP_ID_25675853 5391 RMVar_ID_5391 Human_SNP_ID_704673191 A-to-I Human chr22 - 41930815 41930814 41930815 AAAAAAAAAGACTTGAATAAAGAAATTAGGCCAGGAGTGGTGGCTCATGCCTGTAATCCCAGCAC AAAAAAAAAGACTTGAATAAAGAAATTAGGCC_GGAGTGGTGGCTCATGCCTGTAATCCCAGCAC CT C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1318284504 Functional Loss DEL dbSNP153 33..33 33 - - - 5392 RMVar_ID_5392 Human_SNP_ID_704674796 A-to-I Human chr22 - 41936874 41936874 41936874 CGCCCAGGCTGGAGTGCAGTGGCGTGATCTCAACTCACTGCAGCCTCTGCTCCCTGGTTCAAGTG CGCCCAGGCTGGAGTGCAGTGGCGTGATCTCAGCTCACTGCAGCCTCTGCTCCCTGGTTCAAGTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1303335696 Functional Loss SNV dbSNP153 33..33 33 - - - 5393 RMVar_ID_5393 Human_SNP_ID_704675157 A-to-I Human chr22 - 41938256 41938256 41938256 AGGCCTGTAGTCTCAACTACTCGGGAGGCTGAAGCAGGAGAATCACTTGAACCTGGGAGGCGGAG AGGCCTGTAGTCTCAACTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCTGGGAGGCGGAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1569424937 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25676094 5394 RMVar_ID_5394 Human_SNP_ID_704675184 A-to-I Human chr22 - 41938341 41938341 41938341 AAAAAAAAAAGCGAGACCAGCCTGGCCAACATAGTGAAACCCTGTCTCTACTAAAAATACAAAAA AAAAAAAAAAGCGAGACCAGCCTGGCCAACATGGTGAAACCCTGTCTCTACTAAAAATACAAAAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1400167351 Functional Loss SNV dbSNP153 33..33 33 - - - 5395 RMVar_ID_5395 Human_SNP_ID_704711762 A-to-I Human chr22 + 42079904 42079904 42079904 GGAGCGGCTCAGGCCGGAGCCTGGTACCGTCGAGGTCAGTCATCGTTACCCGCAGCGGCGCCATT GGAGCGGCTCAGGCCGGAGCCTGGTACCGTCGGGGTCAGTCATCGTTACCCGCAGCGGCGCCATT A G SMDT1 Ensembl:ENSG00000183172 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs17852210 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_582015,Human_RBP_ID_4702245,Human_RBP_ID_26822628 Human_Splice_Rec_2172029,Human_Splice_Rec_2172033,Human_Splice_Rec_2172035 5396 RMVar_ID_5396 Human_SNP_ID_704714885 A-to-I Human chr22 + 42090712 42090712 42090712 CTGAAAATGGGCTTCACGAAGGTGCTGGCGGTAGAAGTAGCTTGGCGGACGCCGCTCCCCGCCAT CTGAAAATGGGCTTCACGAAGGTGCTGGCGGTGGAAGTAGCTTGGCGGACGCCGCTCCCCGCCAT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs762811777 Functional Loss SNV dbSNP153 33..33 33 - - - 5397 RMVar_ID_5397 Human_SNP_ID_704719495 A-to-I Human chr22 - 42108411 42108411 42108411 CTGTGAGAGGAGGAGATAAAAAACTAAAACCCAAATATGATATAATGTGCAAAGTAAAATCCTGG CTGTGAGAGGAGGAGATAAAAAACTAAAACCCGAATATGATATAATGTGCAAAGTAAAATCCTGG T C OLA1P1 Ensembl:ENSG00000213790 Pseudogene exon GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs878925875 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17583817,Human_RBP_ID_26499204 5398 RMVar_ID_5398 Human_SNP_ID_704723374 A-to-I Human chr22 + 42122974 42122974 42122974 CCTTAGGTGGCCCAGGCTGGTGTTGAATTCCTAGGCTCAAACAATCCTCCTGCCTTAGCCTCCCA CCTTAGGTGGCCCAGGCTGGTGTTGAATTCCTCGGCTCAAACAATCCTCCTGCCTTAGCCTCCCA A C NDUFA6-DT Ensembl:ENSG00000237037 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1218412526 Functional Loss SNV dbSNP153 33..33 33 - - - 5399 RMVar_ID_5399 Human_SNP_ID_704762063 A-to-I Human chr22 - 42244967 42244967 42244967 GCAAATCTTGTGCCTCAACCACCCCAGTAGCTAGGATTACAGGTGCGCACCACCATGCCCAGCTG GCAAATCTTGTGCCTCAACCACCCCAGTAGCTGGGATTACAGGTGCGCACCACCATGCCCAGCTG T C TCF20 Ensembl:ENSG00000100207 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1035487535 Functional Loss SNV dbSNP153 33..33 33 - - - 5400 RMVar_ID_5400 Human_SNP_ID_704763918 A-to-I Human chr22 - 42251631 42251631 42251631 AGGCATGGTTGCAAGTGCCTGTAGTCCCCGCTACTCGGGATGCTGAGGCACGAGAATCACTTGAA AGGCATGGTTGCAAGTGCCTGTAGTCCCCGCTGCTCGGGATGCTGAGGCACGAGAATCACTTGAA T C TCF20 Ensembl:ENSG00000100207 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879457902 Functional Loss SNV dbSNP153 33..33 33 - - - 5401 RMVar_ID_5401 Human_SNP_ID_704767854 A-to-I Human chr22 - 42265387 42265387 42265387 TGAGGATCATTTGAACCTGAGAGGTTGAGGCTACAGTGAGCCATGTTGTTGCCATTGTACTCCAG TGAGGATCATTTGAACCTGAGAGGTTGAGGCTGCAGTGAGCCATGTTGTTGCCATTGTACTCCAG T C TCF20 Ensembl:ENSG00000100207 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs557663030 Functional Loss SNV dbSNP153 33..33 33 - - - 5402 RMVar_ID_5402 Human_SNP_ID_704768504 A-to-I Human chr22 - 42267618 42267618 42267618 CGGCCCACTGTAACCTCCGCCTCCCGGGTTCAAGCAATTCTCCCACCTCAGCCTCCTGAGTAGCT CGGCCCACTGTAACCTCCGCCTCCCGGGTTCAGGCAATTCTCCCACCTCAGCCTCCTGAGTAGCT T C TCF20 Ensembl:ENSG00000100207 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs568535644 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14514024 5403 RMVar_ID_5403 Human_SNP_ID_704782438 A-to-I Human chr22 - 42321690 42321690 42321690 GGCCCACCTCCGCCTTCCAAAGTGCTAGGATTACAGGTGTGAGTCACCGCGCCCAGCCTGGTCCC GGCCCACCTCCGCCTTCCAAAGTGCTAGGATTTCAGGTGTGAGTCACCGCGCCCAGCCTGGTCCC T A TCF20 Ensembl:ENSG00000100207 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs977209375 Functional Loss SNV dbSNP153 33..33 33 - - - 5404 RMVar_ID_5404 Human_SNP_ID_704816602 A-to-I Human chr22 + 42450756 42450756 42450756 ACAAGAGTTGGAGGTTTCAGTGAGCTGAGATTACGCTATTGCACTCCAGCCTGGGCGGCAGAGTG ACAAGAGTTGGAGGTTTCAGTGAGCTGAGATTGCGCTATTGCACTCCAGCCTGGGCGGCAGAGTG A G - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs574198935 Functional Loss SNV dbSNP153 33..33 33 - - - 5405 RMVar_ID_5405 Human_SNP_ID_704836247 A-to-I Human chr22 - 42517057 42517057 42517057 GCCAGGCTGGTCTCGAACTGCTGACCTGAAGTAATCCGCCCCCTTCAGCCTCCCAACGTGCTGGG GCCAGGCTGGTCTCGAACTGCTGACCTGAAGTTATCCGCCCCCTTCAGCCTCCCAACGTGCTGGG T A RRP7A Ensembl:ENSG00000189306 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1482707095 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93865,RMVar_hsa_circ_214789,RMVar_hsa_circ_80340,RMVar_hsa_circ_214791 5406 RMVar_ID_5406 Human_SNP_ID_704836285 A-to-I Human chr22 - 42517169 42517169 42517169 GGTTCAAGTGATTCTCCTGCCGCAGCCTCCCAAGCAGCTGGAATTACAGGCGCCCACCACCATGC GGTTCAAGTGATTCTCCTGCCGCAGCCTCCCAGGCAGCTGGAATTACAGGCGCCCACCACCATGC T C RRP7A Ensembl:ENSG00000189306 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs983009583 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93865,RMVar_hsa_circ_214789,RMVar_hsa_circ_80340,RMVar_hsa_circ_214791 5407 RMVar_ID_5407 Human_SNP_ID_704836286 A-to-I Human chr22 - 42517170 42517170 42517170 GGGTTCAAGTGATTCTCCTGCCGCAGCCTCCCAAGCAGCTGGAATTACAGGCGCCCACCACCATG GGGTTCAAGTGATTCTCCTGCCGCAGCCTCCCGAGCAGCTGGAATTACAGGCGCCCACCACCATG T C RRP7A Ensembl:ENSG00000189306 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs908311293 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93865,RMVar_hsa_circ_214789,RMVar_hsa_circ_80340,RMVar_hsa_circ_214791 5408 RMVar_ID_5408 Human_SNP_ID_704836305 A-to-I Human chr22 - 42517215 42517215 42517215 AGGCTGGAGCACAGCGTTCACAACTCACTGCAACCTCCGCTTCCCGGGTTCAAGTGATTCTCCTG AGGCTGGAGCACAGCGTTCACAACTCACTGCAGCCTCCGCTTCCCGGGTTCAAGTGATTCTCCTG T C RRP7A Ensembl:ENSG00000189306 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350515101 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93865,RMVar_hsa_circ_214789,RMVar_hsa_circ_80340,RMVar_hsa_circ_214791 5409 RMVar_ID_5409 Human_SNP_ID_704852422 A-to-I Human chr22 - 42567617 42567617 42567617 GCCCAGGCCGGACTGCGAACTGCAGTGGCGCAATCTCGGCTCACTGCAAGCTCTGCTTCCCGGGT GCCCAGGCCGGACTGCGAACTGCAGTGGCGCAGTCTCGGCTCACTGCAAGCTCTGCTTCCCGGGT T C RRP7BP Ensembl:ENSG00000182841 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1393466737 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8262587,Human_RBP_ID_18516496 RMVar_hsa_circ_93865,RMVar_hsa_circ_214789,RMVar_hsa_circ_80340,RMVar_hsa_circ_96579,RMVar_hsa_circ_214791,RMVar_hsa_circ_214792 5410 RMVar_ID_5410 Human_SNP_ID_704852676 A-to-I Human chr22 - 42568162 42568162 42568162 AAATTTAGCTGGGTGTGGTAGCGCACACCTGTAGTCCTAGCCACTCCGGAGGCTGAGGTGGGAAG AAATTTAGCTGGGTGTGGTAGCGCACACCTGTCGTCCTAGCCACTCCGGAGGCTGAGGTGGGAAG T G RRP7BP Ensembl:ENSG00000182841 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs911938198 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18516738 RMVar_hsa_circ_93865,RMVar_hsa_circ_214789,RMVar_hsa_circ_80340,RMVar_hsa_circ_96579,RMVar_hsa_circ_214791,RMVar_hsa_circ_214792 5411 RMVar_ID_5411 Human_SNP_ID_704852684 A-to-I Human chr22 - 42568175 42568175 42568175 CTACAAAAGTAAAAAATTTAGCTGGGTGTGGTAGCGCACACCTGTAGTCCTAGCCACTCCGGAGG CTACAAAAGTAAAAAATTTAGCTGGGTGTGGTGGCGCACACCTGTAGTCCTAGCCACTCCGGAGG T C RRP7BP Ensembl:ENSG00000182841 Pseudogene intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1432851550 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93865,RMVar_hsa_circ_214789,RMVar_hsa_circ_80340,RMVar_hsa_circ_96579,RMVar_hsa_circ_214791,RMVar_hsa_circ_214792 5412 RMVar_ID_5412 Human_SNP_ID_704852906 A-to-I Human chr22 - 42568785 42568785 42568785 ATTTTTGTATTTTTTGGTAGAGACAGGGTTTCACCATGTTGGCGAGGCTGGTCTTTAACTCCTGG ATTTTTGTATTTTTTGGTAGAGACAGGGTTTCCCCATGTTGGCGAGGCTGGTCTTTAACTCCTGG T G RRP7BP Ensembl:ENSG00000182841 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1213664706 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93865,RMVar_hsa_circ_214789,RMVar_hsa_circ_80340,RMVar_hsa_circ_96579,RMVar_hsa_circ_214791,RMVar_hsa_circ_214792 5413 RMVar_ID_5413 Human_SNP_ID_704852949 A-to-I Human chr22 - 42568914 42568914 42568914 TCCCACCACTGCACTCCAGCCTGGGCGATCTCAGCTCACTGCAATCTCCGCCTCCCGAGTTAAAG TCCCACCACTGCACTCCAGCCTGGGCGATCTCCGCTCACTGCAATCTCCGCCTCCCGAGTTAAAG T G RRP7BP Ensembl:ENSG00000182841 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs914887308 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93865,RMVar_hsa_circ_214789,RMVar_hsa_circ_80340,RMVar_hsa_circ_96579,RMVar_hsa_circ_214791,RMVar_hsa_circ_214792 5414 RMVar_ID_5414 Human_SNP_ID_704853191 A-to-I Human chr22 - 42569484 42569484 42569484 AAGCTGAGGCAGGTGGATCGCCTGAGGTCAGAAGTTCGAGACCAGTTTGGCAAACGTGGTGAAAC AAGCTGAGGCAGGTGGATCGCCTGAGGTCAGACGTTCGAGACCAGTTTGGCAAACGTGGTGAAAC T G RRP7BP Ensembl:ENSG00000182841 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1368599023 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17400249 RMVar_hsa_circ_93865,RMVar_hsa_circ_214789,RMVar_hsa_circ_80340,RMVar_hsa_circ_96579,RMVar_hsa_circ_214791,RMVar_hsa_circ_214792 5415 RMVar_ID_5415 Human_SNP_ID_704853524 A-to-I Human chr22 - 42570256 42570256 42570256 TGCGCCACCAGGCCTAATTTTGTATTTTTAGTAGCGACAGGGTTTCACCATGTTGGTCAGGCTGG TGCGCCACCAGGCCTAATTTTGTATTTTTAGTCGCGACAGGGTTTCACCATGTTGGTCAGGCTGG T G RRP7BP Ensembl:ENSG00000182841 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs533589164 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93865,RMVar_hsa_circ_214789,RMVar_hsa_circ_80340,RMVar_hsa_circ_96579,RMVar_hsa_circ_214791,RMVar_hsa_circ_214792 5416 RMVar_ID_5416 Human_SNP_ID_704857386 A-to-I Human chr22 - 42579055 42579055 42579055 ACGACTCACTGCAACCTCCACTTCCTGGGTTCAAGCGATTCTCCTGCCACAGCATCCCGAGCAGC ACGACTCACTGCAACCTCCACTTCCTGGGTTCGAGCGATTCTCCTGCCACAGCATCCCGAGCAGC T C RRP7BP Ensembl:ENSG00000182841 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1386664346 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4702802,Human_RBP_ID_17400735 RMVar_hsa_circ_96579,RMVar_hsa_circ_214792,RMVar_hsa_circ_372848,RMVar_hsa_circ_214795 5417 RMVar_ID_5417 Human_SNP_ID_704859789 A-to-I Human chr22 - 42586164 42586162 42586165 GTAGTCCTAGCTCCTTAGGAGGCTGTGGCAGGAGAACTGCTTGAGCCTAGGAGATGGAGGCTGAT GTAGTCCTAGCTCCTTAGGAGGCTGTGGCAG___AACTGCTTGAGCCTAGGAGATGGAGGCTGAT TCTC T POLDIP3 Ensembl:ENSG00000100227 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947188790 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_105860,RMVar_hsa_circ_114548,RMVar_hsa_circ_214796,RMVar_hsa_circ_96290,RMVar_hsa_circ_214798,RMVar_hsa_circ_214797 5418 RMVar_ID_5418 Human_SNP_ID_704859793 A-to-I Human chr22 - 42586180 42586180 42586180 ATGGTGGTACACGCCTGTAGTCCTAGCTCCTTAGGAGGCTGTGGCAGGAGAACTGCTTGAGCCTA ATGGTGGTACACGCCTGTAGTCCTAGCTCCTTCGGAGGCTGTGGCAGGAGAACTGCTTGAGCCTA T G POLDIP3 Ensembl:ENSG00000100227 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1374940290 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105860,RMVar_hsa_circ_114548,RMVar_hsa_circ_214796,RMVar_hsa_circ_96290,RMVar_hsa_circ_214798,RMVar_hsa_circ_214797 5419 RMVar_ID_5419 Human_SNP_ID_704860551 A-to-I Human chr22 - 42588798 42588798 42588798 TATGAGGAAACCCCATCTCTACTAAAAATACAAAATTAGCCAGGTGTGGTGGTACATGCCTGTAA TATGAGGAAACCCCATCTCTACTAAAAATACAGAATTAGCCAGGTGTGGTGGTACATGCCTGTAA T C POLDIP3 Ensembl:ENSG00000100227 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs887902718 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105860,RMVar_hsa_circ_114548,RMVar_hsa_circ_214796,RMVar_hsa_circ_96290,RMVar_hsa_circ_214798,RMVar_hsa_circ_214797 5420 RMVar_ID_5420 Human_SNP_ID_704860552 A-to-I Human chr22 - 42588798 42588798 42588798 TATGAGGAAACCCCATCTCTACTAAAAATACAAAATTAGCCAGGTGTGGTGGTACATGCCTGTAA TATGAGGAAACCCCATCTCTACTAAAAATACACAATTAGCCAGGTGTGGTGGTACATGCCTGTAA T G POLDIP3 Ensembl:ENSG00000100227 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs887902718 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105860,RMVar_hsa_circ_114548,RMVar_hsa_circ_214796,RMVar_hsa_circ_96290,RMVar_hsa_circ_214798,RMVar_hsa_circ_214797 5421 RMVar_ID_5421 Human_SNP_ID_704860564 A-to-I Human chr22 - 42588832 42588832 42588832 CACCTGATTGGGAGTTCGAGACCAGCTTGACCAATATGAGGAAACCCCATCTCTACTAAAAATAC CACCTGATTGGGAGTTCGAGACCAGCTTGACCGATATGAGGAAACCCCATCTCTACTAAAAATAC T C POLDIP3 Ensembl:ENSG00000100227 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1356371847 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105860,RMVar_hsa_circ_114548,RMVar_hsa_circ_214796,RMVar_hsa_circ_96290,RMVar_hsa_circ_214798,RMVar_hsa_circ_214797 5422 RMVar_ID_5422 Human_SNP_ID_704860972 A-to-I Human chr22 - 42590355 42590355 42590355 ACGTGGCAAGACCCTGTCTCAAAAAATAAATTAGCTGGGCGCGTGGTGGCGTGTGCCTGTAGTCC ACGTGGCAAGACCCTGTCTCAAAAAATAAATTGGCTGGGCGCGTGGTGGCGTGTGCCTGTAGTCC T C POLDIP3 Ensembl:ENSG00000100227 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1204068765 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105860,RMVar_hsa_circ_114548,RMVar_hsa_circ_214796,RMVar_hsa_circ_96290,RMVar_hsa_circ_214798,RMVar_hsa_circ_214797 5423 RMVar_ID_5423 Human_SNP_ID_704875222 A-to-I Human chr22 - 42633744 42633744 42633744 ACTTTCGCTCTTGTTGCCCAGGCTGGAGTGCAATGGCACAATCTCGACTCACCGCAACCTCCACT ACTTTCGCTCTTGTTGCCCAGGCTGGAGTGCAGTGGCACAATCTCGACTCACCGCAACCTCCACT T C CYB5R3 Ensembl:ENSG00000100243 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1297040879 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_377343,RMVar_hsa_circ_214806,RMVar_hsa_circ_99591,RMVar_hsa_circ_352613 5424 RMVar_ID_5424 Human_SNP_ID_704899032 A-to-I Human chr22 - 42715948 42715932 42715949 CATTCCTGTAATCCCACCTACTCAGGAGGCTGAGGCAGAAGAATCGCTTGAACGCAGGAGGCGGA CATTCCTGTAATCCCACCTACTCAGGAGGCT_________________TGAACGCAGGAGGCGGA AAGCGATTCTTCTGCCTC A A4GALT Ensembl:ENSG00000128274 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1333567350 Functional Loss DEL dbSNP153 32..48 33 - - - 5425 RMVar_ID_5425 Human_SNP_ID_704899080 A-to-I Human chr22 - 42716113 42716113 42716113 AATTATATTTCTGAGGCCGGGCGCAGTGGTTCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAA AATTATATTTCTGAGGCCGGGCGCAGTGGTTCGTGCCTGTAATCCCAGCACTTTGGGAGGCCGAA T C A4GALT Ensembl:ENSG00000128274 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1200772904 Functional Loss SNV dbSNP153 33..33 33 - - - 5426 RMVar_ID_5426 Human_SNP_ID_704926336 A-to-I Human chr22 - 42810003 42810002 42810004 TCCCCAATTTTTTTTTTTTTTTTTTTTTTTTTAAGATGGAGTCTTGCTCTGTCACCCAGGCTGGA TCCCCAATTTTTTTTTTTTTTTTTTTTTTTT__AGATGGAGTCTTGCTCTGTCACCCAGGCTGGA TTA T ARFGAP3 Ensembl:ENSG00000242247 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1491333876 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_22634,RMVar_hsa_circ_15451,RMVar_hsa_circ_287958,RMVar_hsa_circ_339625,RMVar_hsa_circ_64051,RMVar_hsa_circ_68856,RMVar_hsa_circ_214811,RMVar_hsa_circ_214812,RMVar_hsa_circ_324087,RMVar_hsa_circ_346051,RMVar_hsa_circ_31222,RMVar_hsa_circ_214814,RMVar_hsa_circ_214815,RMVar_hsa_circ_87698,RMVar_hsa_circ_358578 5427 RMVar_ID_5427 Human_SNP_ID_704926344 A-to-I Human chr22 - 42810003 42810003 42810003 TCCCCAATTTTTTTTTTTTTTTTTTTTTTTTTAAGATGGAGTCTTGCTCTGTCACCCAGGCTGGA TCCCCAATTTTTTTTTTTTTTTTTTTTTTTTTTAGATGGAGTCTTGCTCTGTCACCCAGGCTGGA T A ARFGAP3 Ensembl:ENSG00000242247 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1461909869 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22634,RMVar_hsa_circ_15451,RMVar_hsa_circ_287958,RMVar_hsa_circ_339625,RMVar_hsa_circ_64051,RMVar_hsa_circ_68856,RMVar_hsa_circ_214811,RMVar_hsa_circ_214812,RMVar_hsa_circ_324087,RMVar_hsa_circ_346051,RMVar_hsa_circ_31222,RMVar_hsa_circ_214814,RMVar_hsa_circ_214815,RMVar_hsa_circ_87698,RMVar_hsa_circ_358578 5428 RMVar_ID_5428 Human_SNP_ID_704926345 A-to-I Human chr22 - 42810003 42810003 42810003 TCCCCAATTTTTTTTTTTTTTTTTTTTTTTTTAAGATGGAGTCTTGCTCTGTCACCCAGGCTGGA TCCCCAATTTTTTTTTTTTTTTTTTTTTTTTTGAGATGGAGTCTTGCTCTGTCACCCAGGCTGGA T C ARFGAP3 Ensembl:ENSG00000242247 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1461909869 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22634,RMVar_hsa_circ_15451,RMVar_hsa_circ_287958,RMVar_hsa_circ_339625,RMVar_hsa_circ_64051,RMVar_hsa_circ_68856,RMVar_hsa_circ_214811,RMVar_hsa_circ_214812,RMVar_hsa_circ_324087,RMVar_hsa_circ_346051,RMVar_hsa_circ_31222,RMVar_hsa_circ_214814,RMVar_hsa_circ_214815,RMVar_hsa_circ_87698,RMVar_hsa_circ_358578 5429 RMVar_ID_5429 Human_SNP_ID_704930074 A-to-I Human chr22 - 42825169 42825169 42825169 GTTCACTGCAGCCTGGCCCAAGAGATTCTCCTACCTCAGCCTCCCAAGTAGCTGGGACCACAGGC GTTCACTGCAGCCTGGCCCAAGAGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACCACAGGC T C ARFGAP3 Ensembl:ENSG00000242247 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968913259 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25676828 RMVar_hsa_circ_214819,RMVar_hsa_circ_22634,RMVar_hsa_circ_15451,RMVar_hsa_circ_287958,RMVar_hsa_circ_214812,RMVar_hsa_circ_346051,RMVar_hsa_circ_69170,RMVar_hsa_circ_214815,RMVar_hsa_circ_87698,RMVar_hsa_circ_358578,RMVar_hsa_circ_364626,RMVar_hsa_circ_327237,RMVar_hsa_circ_328404,RMVar_hsa_circ_100099,RMVar_hsa_circ_28705,RMVar_hsa_circ_214820,RMVar_hsa_circ_60259,RMVar_hsa_circ_214818,RMVar_hsa_circ_317501,RMVar_hsa_circ_214823 5430 RMVar_ID_5430 Human_SNP_ID_704930674 A-to-I Human chr22 - 42827443 42827443 42827443 ATAATGGCTTGAACCCGGGAGGCGAAGGTTGCAGTGAGCCGAGATCGTGCCATTGCACTCCAGCT ATAATGGCTTGAACCCGGGAGGCGAAGGTTGCCGTGAGCCGAGATCGTGCCATTGCACTCCAGCT T G ARFGAP3 Ensembl:ENSG00000242247 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1016461770 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_214819,RMVar_hsa_circ_22634,RMVar_hsa_circ_15451,RMVar_hsa_circ_287958,RMVar_hsa_circ_214812,RMVar_hsa_circ_346051,RMVar_hsa_circ_69170,RMVar_hsa_circ_214815,RMVar_hsa_circ_87698,RMVar_hsa_circ_327237,RMVar_hsa_circ_100099,RMVar_hsa_circ_28705,RMVar_hsa_circ_68745,RMVar_hsa_circ_60259,RMVar_hsa_circ_214818,RMVar_hsa_circ_317501,RMVar_hsa_circ_318145,RMVar_hsa_circ_214823,RMVar_hsa_circ_329883,RMVar_hsa_circ_274758,RMVar_hsa_circ_214824,RMVar_hsa_circ_214825 5431 RMVar_ID_5431 Human_SNP_ID_704930800 A-to-I Human chr22 - 42827917 42827916 42827917 AGTATGGTTGGGCGCGGTAGCTCACGCCTGTAATACCAACACTTTGGGAGGCCAAGGTGGGAGGT AGTATGGTTGGGCGCGGTAGCTCACGCCTGTA_TACCAACACTTTGGGAGGCCAAGGTGGGAGGT AT A ARFGAP3 Ensembl:ENSG00000242247 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs961678624 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_17572860 RMVar_hsa_circ_214819,RMVar_hsa_circ_22634,RMVar_hsa_circ_15451,RMVar_hsa_circ_287958,RMVar_hsa_circ_214812,RMVar_hsa_circ_346051,RMVar_hsa_circ_69170,RMVar_hsa_circ_214815,RMVar_hsa_circ_87698,RMVar_hsa_circ_327237,RMVar_hsa_circ_100099,RMVar_hsa_circ_28705,RMVar_hsa_circ_68745,RMVar_hsa_circ_60259,RMVar_hsa_circ_214818,RMVar_hsa_circ_317501,RMVar_hsa_circ_318145,RMVar_hsa_circ_214823,RMVar_hsa_circ_329883,RMVar_hsa_circ_274758,RMVar_hsa_circ_214824,RMVar_hsa_circ_214825 5432 RMVar_ID_5432 Human_SNP_ID_704930801 A-to-I Human chr22 - 42827918 42827918 42827918 AAGTATGGTTGGGCGCGGTAGCTCACGCCTGTAATACCAACACTTTGGGAGGCCAAGGTGGGAGG AAGTATGGTTGGGCGCGGTAGCTCACGCCTGTGATACCAACACTTTGGGAGGCCAAGGTGGGAGG T C ARFGAP3 Ensembl:ENSG00000242247 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs899021982 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17572860 RMVar_hsa_circ_214819,RMVar_hsa_circ_22634,RMVar_hsa_circ_15451,RMVar_hsa_circ_287958,RMVar_hsa_circ_214812,RMVar_hsa_circ_346051,RMVar_hsa_circ_69170,RMVar_hsa_circ_214815,RMVar_hsa_circ_87698,RMVar_hsa_circ_327237,RMVar_hsa_circ_100099,RMVar_hsa_circ_28705,RMVar_hsa_circ_68745,RMVar_hsa_circ_60259,RMVar_hsa_circ_214818,RMVar_hsa_circ_317501,RMVar_hsa_circ_318145,RMVar_hsa_circ_214823,RMVar_hsa_circ_329883,RMVar_hsa_circ_274758,RMVar_hsa_circ_214824,RMVar_hsa_circ_214825 5433 RMVar_ID_5433 Human_SNP_ID_704930802 A-to-I Human chr22 - 42827918 42827918 42827918 AAGTATGGTTGGGCGCGGTAGCTCACGCCTGTAATACCAACACTTTGGGAGGCCAAGGTGGGAGG AAGTATGGTTGGGCGCGGTAGCTCACGCCTGTCATACCAACACTTTGGGAGGCCAAGGTGGGAGG T G ARFGAP3 Ensembl:ENSG00000242247 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs899021982 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17572860 RMVar_hsa_circ_214819,RMVar_hsa_circ_22634,RMVar_hsa_circ_15451,RMVar_hsa_circ_287958,RMVar_hsa_circ_214812,RMVar_hsa_circ_346051,RMVar_hsa_circ_69170,RMVar_hsa_circ_214815,RMVar_hsa_circ_87698,RMVar_hsa_circ_327237,RMVar_hsa_circ_100099,RMVar_hsa_circ_28705,RMVar_hsa_circ_68745,RMVar_hsa_circ_60259,RMVar_hsa_circ_214818,RMVar_hsa_circ_317501,RMVar_hsa_circ_318145,RMVar_hsa_circ_214823,RMVar_hsa_circ_329883,RMVar_hsa_circ_274758,RMVar_hsa_circ_214824,RMVar_hsa_circ_214825 5434 RMVar_ID_5434 Human_SNP_ID_704930807 A-to-I Human chr22 - 42827931 42827931 42827931 AATTAAAATAACAAAGTATGGTTGGGCGCGGTAGCTCACGCCTGTAATACCAACACTTTGGGAGG AATTAAAATAACAAAGTATGGTTGGGCGCGGTGGCTCACGCCTGTAATACCAACACTTTGGGAGG T C ARFGAP3 Ensembl:ENSG00000242247 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1026100535 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17572860 RMVar_hsa_circ_214819,RMVar_hsa_circ_22634,RMVar_hsa_circ_15451,RMVar_hsa_circ_287958,RMVar_hsa_circ_214812,RMVar_hsa_circ_346051,RMVar_hsa_circ_69170,RMVar_hsa_circ_214815,RMVar_hsa_circ_87698,RMVar_hsa_circ_327237,RMVar_hsa_circ_100099,RMVar_hsa_circ_28705,RMVar_hsa_circ_68745,RMVar_hsa_circ_60259,RMVar_hsa_circ_214818,RMVar_hsa_circ_317501,RMVar_hsa_circ_318145,RMVar_hsa_circ_214823,RMVar_hsa_circ_329883,RMVar_hsa_circ_274758,RMVar_hsa_circ_214824,RMVar_hsa_circ_214825 5435 RMVar_ID_5435 Human_SNP_ID_704930898 A-to-I Human chr22 - 42828249 42828248 42828249 TGGCCCTCATCTTTGTATTTTTTAGTAGATACAGGGTTTCACCATGTTGGCCAGGCTGATCTTGA TGGCCCTCATCTTTGTATTTTTTAGTAGATAC_GGGTTTCACCATGTTGGCCAGGCTGATCTTGA CT C ARFGAP3 Ensembl:ENSG00000242247 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1228560615 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_214819,RMVar_hsa_circ_22634,RMVar_hsa_circ_15451,RMVar_hsa_circ_287958,RMVar_hsa_circ_214812,RMVar_hsa_circ_346051,RMVar_hsa_circ_69170,RMVar_hsa_circ_214815,RMVar_hsa_circ_87698,RMVar_hsa_circ_327237,RMVar_hsa_circ_100099,RMVar_hsa_circ_28705,RMVar_hsa_circ_68745,RMVar_hsa_circ_60259,RMVar_hsa_circ_214818,RMVar_hsa_circ_317501,RMVar_hsa_circ_318145,RMVar_hsa_circ_214823,RMVar_hsa_circ_329883,RMVar_hsa_circ_274758,RMVar_hsa_circ_214824,RMVar_hsa_circ_214825 5436 RMVar_ID_5436 Human_SNP_ID_704930899 A-to-I Human chr22 - 42828249 42828249 42828249 TGGCCCTCATCTTTGTATTTTTTAGTAGATACAGGGTTTCACCATGTTGGCCAGGCTGATCTTGA TGGCCCTCATCTTTGTATTTTTTAGTAGATACGGGGTTTCACCATGTTGGCCAGGCTGATCTTGA T C ARFGAP3 Ensembl:ENSG00000242247 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1429062910 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_214819,RMVar_hsa_circ_22634,RMVar_hsa_circ_15451,RMVar_hsa_circ_287958,RMVar_hsa_circ_214812,RMVar_hsa_circ_346051,RMVar_hsa_circ_69170,RMVar_hsa_circ_214815,RMVar_hsa_circ_87698,RMVar_hsa_circ_327237,RMVar_hsa_circ_100099,RMVar_hsa_circ_28705,RMVar_hsa_circ_68745,RMVar_hsa_circ_60259,RMVar_hsa_circ_214818,RMVar_hsa_circ_317501,RMVar_hsa_circ_318145,RMVar_hsa_circ_214823,RMVar_hsa_circ_329883,RMVar_hsa_circ_274758,RMVar_hsa_circ_214824,RMVar_hsa_circ_214825 5437 RMVar_ID_5437 Human_SNP_ID_704930918 A-to-I Human chr22 - 42828300 42828300 42828300 TCCCCCTTGGCCTCCCAAAGTGCCGGGATTACAGGTGTGAGCTACCGCGCCTGGCCCTCATCTTT TCCCCCTTGGCCTCCCAAAGTGCCGGGATTACGGGTGTGAGCTACCGCGCCTGGCCCTCATCTTT T C ARFGAP3 Ensembl:ENSG00000242247 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs929088197 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_214819,RMVar_hsa_circ_22634,RMVar_hsa_circ_15451,RMVar_hsa_circ_287958,RMVar_hsa_circ_214812,RMVar_hsa_circ_346051,RMVar_hsa_circ_69170,RMVar_hsa_circ_214815,RMVar_hsa_circ_87698,RMVar_hsa_circ_327237,RMVar_hsa_circ_100099,RMVar_hsa_circ_28705,RMVar_hsa_circ_68745,RMVar_hsa_circ_60259,RMVar_hsa_circ_214818,RMVar_hsa_circ_317501,RMVar_hsa_circ_318145,RMVar_hsa_circ_214823,RMVar_hsa_circ_329883,RMVar_hsa_circ_274758,RMVar_hsa_circ_214824,RMVar_hsa_circ_214825 5438 RMVar_ID_5438 Human_SNP_ID_704930946 A-to-I Human chr22 - 42828401 42828401 42828401 CAGGCATGTGCCACCACTCCTGGCTAATTTTTATATTTTTAGTAGAGACGGGTTTCACCATGTTG CAGGCATGTGCCACCACTCCTGGCTAATTTTTGTATTTTTAGTAGAGACGGGTTTCACCATGTTG T C ARFGAP3 Ensembl:ENSG00000242247 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs56138607 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_214819,RMVar_hsa_circ_22634,RMVar_hsa_circ_15451,RMVar_hsa_circ_287958,RMVar_hsa_circ_214812,RMVar_hsa_circ_346051,RMVar_hsa_circ_69170,RMVar_hsa_circ_214815,RMVar_hsa_circ_87698,RMVar_hsa_circ_327237,RMVar_hsa_circ_100099,RMVar_hsa_circ_28705,RMVar_hsa_circ_68745,RMVar_hsa_circ_60259,RMVar_hsa_circ_214818,RMVar_hsa_circ_317501,RMVar_hsa_circ_318145,RMVar_hsa_circ_214823,RMVar_hsa_circ_329883,RMVar_hsa_circ_274758,RMVar_hsa_circ_214824,RMVar_hsa_circ_214825 5439 RMVar_ID_5439 Human_SNP_ID_704931044 A-to-I Human chr22 - 42828739 42828739 42828739 CGGAGGTTGCAGTGAGCCGAGTTCGCACCACTACACTCCGCCTGGGCAACAGAACAGGACTCTGT CGGAGGTTGCAGTGAGCCGAGTTCGCACCACTGCACTCCGCCTGGGCAACAGAACAGGACTCTGT T C ARFGAP3 Ensembl:ENSG00000242247 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs577949807 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_214819,RMVar_hsa_circ_22634,RMVar_hsa_circ_15451,RMVar_hsa_circ_287958,RMVar_hsa_circ_214812,RMVar_hsa_circ_346051,RMVar_hsa_circ_69170,RMVar_hsa_circ_214815,RMVar_hsa_circ_87698,RMVar_hsa_circ_327237,RMVar_hsa_circ_100099,RMVar_hsa_circ_28705,RMVar_hsa_circ_68745,RMVar_hsa_circ_60259,RMVar_hsa_circ_214818,RMVar_hsa_circ_317501,RMVar_hsa_circ_318145,RMVar_hsa_circ_214823,RMVar_hsa_circ_329883,RMVar_hsa_circ_274758,RMVar_hsa_circ_214824,RMVar_hsa_circ_214825 5440 RMVar_ID_5440 Human_SNP_ID_704931073 A-to-I Human chr22 - 42828873 42828873 42828873 CAAGGCCAGCCTGGCCAACATTGCAGGACCCTATCTCTACTAAAAATACAAAAATTAGCCAGGCA CAAGGCCAGCCTGGCCAACATTGCAGGACCCTGTCTCTACTAAAAATACAAAAATTAGCCAGGCA T C ARFGAP3 Ensembl:ENSG00000242247 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1018915775 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_214819,RMVar_hsa_circ_22634,RMVar_hsa_circ_15451,RMVar_hsa_circ_287958,RMVar_hsa_circ_214812,RMVar_hsa_circ_346051,RMVar_hsa_circ_69170,RMVar_hsa_circ_214815,RMVar_hsa_circ_87698,RMVar_hsa_circ_327237,RMVar_hsa_circ_100099,RMVar_hsa_circ_28705,RMVar_hsa_circ_68745,RMVar_hsa_circ_60259,RMVar_hsa_circ_214818,RMVar_hsa_circ_317501,RMVar_hsa_circ_318145,RMVar_hsa_circ_214823,RMVar_hsa_circ_329883,RMVar_hsa_circ_274758,RMVar_hsa_circ_214824,RMVar_hsa_circ_214825 5441 RMVar_ID_5441 Human_SNP_ID_704931074 A-to-I Human chr22 - 42828873 42828873 42828873 CAAGGCCAGCCTGGCCAACATTGCAGGACCCTATCTCTACTAAAAATACAAAAATTAGCCAGGCA CAAGGCCAGCCTGGCCAACATTGCAGGACCCTCTCTCTACTAAAAATACAAAAATTAGCCAGGCA T G ARFGAP3 Ensembl:ENSG00000242247 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1018915775 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_214819,RMVar_hsa_circ_22634,RMVar_hsa_circ_15451,RMVar_hsa_circ_287958,RMVar_hsa_circ_214812,RMVar_hsa_circ_346051,RMVar_hsa_circ_69170,RMVar_hsa_circ_214815,RMVar_hsa_circ_87698,RMVar_hsa_circ_327237,RMVar_hsa_circ_100099,RMVar_hsa_circ_28705,RMVar_hsa_circ_68745,RMVar_hsa_circ_60259,RMVar_hsa_circ_214818,RMVar_hsa_circ_317501,RMVar_hsa_circ_318145,RMVar_hsa_circ_214823,RMVar_hsa_circ_329883,RMVar_hsa_circ_274758,RMVar_hsa_circ_214824,RMVar_hsa_circ_214825 5442 RMVar_ID_5442 Human_SNP_ID_704948353 A-to-I Human chr22 - 42890653 42890653 42890653 TGGAGTGCAGTGGTGCAATCTCAGCTCACTGCAACCTGTGCCTCCTGGGTTCAAGCAATTCTGCC TGGAGTGCAGTGGTGCAATCTCAGCTCACTGCGACCTGTGCCTCCTGGGTTCAAGCAATTCTGCC T C PACSIN2 Ensembl:ENSG00000100266 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1218050229 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_366692,RMVar_hsa_circ_81967,RMVar_hsa_circ_85728,RMVar_hsa_circ_214835,RMVar_hsa_circ_214836,RMVar_hsa_circ_214834,RMVar_hsa_circ_214840,RMVar_hsa_circ_47789,RMVar_hsa_circ_60137,RMVar_hsa_circ_122735,RMVar_hsa_circ_340192,RMVar_hsa_circ_214839,RMVar_hsa_circ_126629,RMVar_hsa_circ_264836 5443 RMVar_ID_5443 Human_SNP_ID_704948358 A-to-I Human chr22 - 42890668 42890668 42890668 CTCTCTCTCCCAGGCTGGAGTGCAGTGGTGCAATCTCAGCTCACTGCAACCTGTGCCTCCTGGGT CTCTCTCTCCCAGGCTGGAGTGCAGTGGTGCAGTCTCAGCTCACTGCAACCTGTGCCTCCTGGGT T C PACSIN2 Ensembl:ENSG00000100266 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1206429699 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_366692,RMVar_hsa_circ_81967,RMVar_hsa_circ_85728,RMVar_hsa_circ_214835,RMVar_hsa_circ_214836,RMVar_hsa_circ_214834,RMVar_hsa_circ_214840,RMVar_hsa_circ_47789,RMVar_hsa_circ_60137,RMVar_hsa_circ_122735,RMVar_hsa_circ_340192,RMVar_hsa_circ_214839,RMVar_hsa_circ_126629,RMVar_hsa_circ_264836 5444 RMVar_ID_5444 Human_SNP_ID_704973105 A-to-I Human chr22 - 42984258 42984258 42984258 TAAAAAGTGCTAAGTGCTAGGTAGTGGGTGGTAGCTCACACCTGTAATCCCAGCACTGTGGGAGG TAAAAAGTGCTAAGTGCTAGGTAGTGGGTGGTGGCTCACACCTGTAATCCCAGCACTGTGGGAGG T C PACSIN2 Ensembl:ENSG00000100266 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs761956899 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5203468,Human_RBP_ID_25676947 RMVar_hsa_circ_85728,RMVar_hsa_circ_214836 5445 RMVar_ID_5445 Human_SNP_ID_704974602 A-to-I Human chr22 - 42989722 42989722 42989722 ATCTCAGCTCACTGCTGCAATCTCTGCCTCCCAGGTTCAAATGATTCTCCTACCTCAGCCTCCCA ATCTCAGCTCACTGCTGCAATCTCTGCCTCCCTGGTTCAAATGATTCTCCTACCTCAGCCTCCCA T A PACSIN2 Ensembl:ENSG00000100266 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1325337399 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85728,RMVar_hsa_circ_214836 5446 RMVar_ID_5446 Human_SNP_ID_704974603 A-to-I Human chr22 - 42989722 42989722 42989722 ATCTCAGCTCACTGCTGCAATCTCTGCCTCCCAGGTTCAAATGATTCTCCTACCTCAGCCTCCCA ATCTCAGCTCACTGCTGCAATCTCTGCCTCCCGGGTTCAAATGATTCTCCTACCTCAGCCTCCCA T C PACSIN2 Ensembl:ENSG00000100266 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1325337399 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85728,RMVar_hsa_circ_214836 5447 RMVar_ID_5447 Human_SNP_ID_704975541 A-to-I Human chr22 - 42992942 42992942 42992942 CCAGGCTGGTCTCAAACTCCTGAGCTCGGGCAATCTGCCCGCCTCAGCCTCCCAGAGTGCTAGGA CCAGGCTGGTCTCAAACTCCTGAGCTCGGGCAGTCTGCCCGCCTCAGCCTCCCAGAGTGCTAGGA T C PACSIN2 Ensembl:ENSG00000100266 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs759762343 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85728,RMVar_hsa_circ_214836 5448 RMVar_ID_5448 Human_SNP_ID_704979764 A-to-I Human chr22 - 43010007 43010007 43010007 AAATTAGTCGGGTATGGTGGCGTGCGCCTATAATCTCAGCTACTCGGGAGGCTGAGGCAGGAGAA AAATTAGTCGGGTATGGTGGCGTGCGCCTATAGTCTCAGCTACTCGGGAGGCTGAGGCAGGAGAA T C PACSIN2 Ensembl:ENSG00000100266 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1365193691 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85728,RMVar_hsa_circ_214836 5449 RMVar_ID_5449 Human_SNP_ID_704979795 A-to-I Human chr22 - 43010147 43010147 43010147 ATAATAAAATGGGGCTGGGCGCTGTGGCTCACACCTGTAATCCCAGCACTATGGGAAGTAAAGGA ATAATAAAATGGGGCTGGGCGCTGTGGCTCACCCCTGTAATCCCAGCACTATGGGAAGTAAAGGA T G PACSIN2 Ensembl:ENSG00000100266 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1020482305 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17572864 RMVar_hsa_circ_85728,RMVar_hsa_circ_214836 5450 RMVar_ID_5450 Human_SNP_ID_704997951 A-to-I Human chr22 - 43074176 43074176 43074176 GTGATCCGCCCGCCTTGGCCTCCCAAAGTGCTAGGATTACAGGCGTGAGCCACTGTGCCTGGCCA GTGATCCGCCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGTGCCTGGCCA T C TTLL1 Ensembl:ENSG00000100271 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1382128877 Functional Loss SNV dbSNP153 33..33 33 - - - 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_354862 5451 RMVar_ID_5451 Human_SNP_ID_705016143 A-to-I Human chr22 - 43136120 43136120 43136120 CCTACCTTAGCCTCCTGAGTGGCTTGGATTACAGACACGGGCAACCACACCTGGCTAACTTTTGT CCTACCTTAGCCTCCTGAGTGGCTTGGATTACTGACACGGGCAACCACACCTGGCTAACTTTTGT T A MCAT Ensembl:ENSG00000100294 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1397040878 Functional Loss SNV dbSNP153 33..33 33 - - - 5452 RMVar_ID_5452 Human_SNP_ID_705016146 A-to-I Human chr22 - 43136149 43136136 43136149 GCCTGGACCTCCTGGGCTCAAGTGTTCCTCCTACCTTAGCCTCCTGAGTGGCTTGGATTACAGAC GCCTGGACCTCCTGGGCTCAAGTGTTCCTCCT_____________GAGTGGCTTGGATTACAGAC CAGGAGGCTAAGGT C MCAT Ensembl:ENSG00000100294 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1242665090 Functional Loss DEL dbSNP153 33..45 33 - - - 5453 RMVar_ID_5453 Human_SNP_ID_705016840 A-to-I Human chr22 - 43138571 43138571 43138571 TGCCACGCCCGGCTAATTTTTGTATTTTTGGTAGTGACAGGGTTTTACCATGTTGTCTAGTCTGG TGCCACGCCCGGCTAATTTTTGTATTTTTGGTGGTGACAGGGTTTTACCATGTTGTCTAGTCTGG T C MCAT Ensembl:ENSG00000100294 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs939616068 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_334529 5454 RMVar_ID_5454 Human_SNP_ID_705016863 A-to-I Human chr22 - 43138650 43138650 43138650 TCACTGTAGCCTCAACTTCCTGGGCTCCAGCAATCCTCCCACCTCAGCCTCCCAAGTAGCTGGGA TCACTGTAGCCTCAACTTCCTGGGCTCCAGCAGTCCTCCCACCTCAGCCTCCCAAGTAGCTGGGA T C MCAT Ensembl:ENSG00000100294 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs879495610 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_334529 5455 RMVar_ID_5455 Human_SNP_ID_705016872 A-to-I Human chr22 - 43138701 43138684 43138701 ACAGGGTCTCGCTCTGTCACCCAGGCTGGAATACAGTGGCATGAACACAGCTCACTGTAGCCTCA ACAGGGTCTCGCTCTGTCACCCAGGCTGGAAT_________________GCTCACTGTAGCCTCA CTGTGTTCATGCCACTGT C MCAT Ensembl:ENSG00000100294 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1305122332 Functional Loss DEL dbSNP153 33..49 33 - - - RMVar_hsa_circ_334529 5456 RMVar_ID_5456 Human_SNP_ID_705017321 A-to-I Human chr22 - 43140505 43140505 43140505 ATCTCTACCGAAAATACAAAAATTAGCCAGGCATGTTGGTGTGCGCCTGTAGTCCCAGCTCGAGT ATCTCTACCGAAAATACAAAAATTAGCCAGGCGTGTTGGTGTGCGCCTGTAGTCCCAGCTCGAGT T C MCAT Ensembl:ENSG00000100294 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs530442157 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_334529 5457 RMVar_ID_5457 Human_SNP_ID_705017329 A-to-I Human chr22 - 43140537 43140537 43140537 TAGACCACCCTGGGCAACATGGTGAAAACCCCATCTCTACCGAAAATACAAAAATTAGCCAGGCA TAGACCACCCTGGGCAACATGGTGAAAACCCCGTCTCTACCGAAAATACAAAAATTAGCCAGGCA T C MCAT Ensembl:ENSG00000100294 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs756469828 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_334529 5458 RMVar_ID_5458 Human_SNP_ID_705238120 A-to-I Human chr22 + 43947220 43947220 43947220 GTCTCTACTAAAAATACAAAAATTATCTGGGCATGGTGGTGCATGCCTGTAATCCCAGCTATTCG GTCTCTACTAAAAATACAAAAATTATCTGGGCGTGGTGGTGCATGCCTGTAATCCCAGCTATTCG A G PNPLA3 Ensembl:ENSG00000100344 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1195863804 Functional Loss SNV dbSNP153 33..33 33 - - - 5459 RMVar_ID_5459 Human_SNP_ID_705238750 A-to-I Human chr22 + 43949526 43949526 43949526 GCATGTGCCACCACGCCCAGCTAATTTTTTGTATTTTTAGTAGAGATGGGGTTTCTCCAGGTTGG GCATGTGCCACCACGCCCAGCTAATTTTTTGTGTTTTTAGTAGAGATGGGGTTTCTCCAGGTTGG A G PNPLA3 Ensembl:ENSG00000100344 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs1484848010 Functional Loss SNV dbSNP153 33..33 33 - - - 5460 RMVar_ID_5460 Human_SNP_ID_705238752 A-to-I Human chr22 + 43949532 43949532 43949532 GCCACCACGCCCAGCTAATTTTTTGTATTTTTAGTAGAGATGGGGTTTCTCCAGGTTGGTCAGGC GCCACCACGCCCAGCTAATTTTTTGTATTTTTGGTAGAGATGGGGTTTCTCCAGGTTGGTCAGGC A G PNPLA3 Ensembl:ENSG00000100344 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229,31158229 RNA-Seq:(High) rs913383072 Functional Loss SNV dbSNP153 33..33 33 - - - 5461 RMVar_ID_5461 Human_SNP_ID_705239072 A-to-I Human chr22 + 43950636 43950636 43950636 GGCAACATTCTTTTTTTTTTTTTTTTTTTTTGAGGCAGGGTCCCGCTCTGTCATCCAGGCTAGAG GGCAACATTCTTTTTTTTTTTTTTTTTTTTTGGGGCAGGGTCCCGCTCTGTCATCCAGGCTAGAG A G PNPLA3 Ensembl:ENSG00000100344 Protein coding intron GSE100210;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229 RNA-Seq:(High) rs1299888180 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14517945 5462 RMVar_ID_5462 Human_SNP_ID_705239073 A-to-I Human chr22 + 43950636 43950636 43950636 GGCAACATTCTTTTTTTTTTTTTTTTTTTTTGAGGCAGGGTCCCGCTCTGTCATCCAGGCTAGAG GGCAACATTCTTTTTTTTTTTTTTTTTTTTTGTGGCAGGGTCCCGCTCTGTCATCCAGGCTAGAG A T PNPLA3 Ensembl:ENSG00000100344 Protein coding intron GSE100210;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229 RNA-Seq:(High) rs1299888180 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14517945 5463 RMVar_ID_5463 Human_SNP_ID_705239083 A-to-I Human chr22 + 43950665 43950665 43950665 TTGAGGCAGGGTCCCGCTCTGTCATCCAGGCTAGAGTACGGTGGTGCAATCATAGTTCACTGCAG TTGAGGCAGGGTCCCGCTCTGTCATCCAGGCTGGAGTACGGTGGTGCAATCATAGTTCACTGCAG A G PNPLA3 Ensembl:ENSG00000100344 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1457923269 Functional Loss SNV dbSNP153 33..33 33 - - - 5464 RMVar_ID_5464 Human_SNP_ID_705239105 A-to-I Human chr22 + 43950774 43950774 43950774 AAGTAGCTGGAACCACATGTGTGCACTACCACACCCAGCTAGTTTTTTTTTGTAGAGACAGGGCC AAGTAGCTGGAACCACATGTGTGCACTACCACGCCCAGCTAGTTTTTTTTTGTAGAGACAGGGCC A G PNPLA3 Ensembl:ENSG00000100344 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913737338 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23951714 5465 RMVar_ID_5465 Human_SNP_ID_705239128 A-to-I Human chr22 + 43950846 43950846 43950846 GTTGCCCAGGCTGGTCTCCAAGTCCTGGGCTCAAGTGATGCTCCTGCCTTGGCCTTCCAAAGTGC GTTGCCCAGGCTGGTCTCCAAGTCCTGGGCTCGAGTGATGCTCCTGCCTTGGCCTTCCAAAGTGC A G PNPLA3 Ensembl:ENSG00000100344 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1257698386 Functional Loss SNV dbSNP153 33..33 33 - - - 5466 RMVar_ID_5466 Human_SNP_ID_705239140 A-to-I Human chr22 + 43950880 43950878 43950880 GTGATGCTCCTGCCTTGGCCTTCCAAAGTGCTAGGATTACAGGTGTGAGCTACCATGCCTGGTCC GTGATGCTCCTGCCTTGGCCTTCCAAAGTGC__GGATTACAGGTGTGAGCTACCATGCCTGGTCC CTA C PNPLA3 Ensembl:ENSG00000100344 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1400438532 Functional Loss DEL dbSNP153 32..33 33 - - - 5467 RMVar_ID_5467 Human_SNP_ID_705239141 A-to-I Human chr22 + 43950880 43950880 43950880 GTGATGCTCCTGCCTTGGCCTTCCAAAGTGCTAGGATTACAGGTGTGAGCTACCATGCCTGGTCC GTGATGCTCCTGCCTTGGCCTTCCAAAGTGCTGGGATTACAGGTGTGAGCTACCATGCCTGGTCC A G PNPLA3 Ensembl:ENSG00000100344 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs573880788 Functional Loss SNV dbSNP153 33..33 33 - - - 5468 RMVar_ID_5468 Human_SNP_ID_705239213 A-to-I Human chr22 + 43951215 43951215 43951215 CCTGTAATCCCAGCAACCAGGGAGGCTGAGGCAGGAGAATCACTTGAACCCAGGAGGTGGAGGTT CCTGTAATCCCAGCAACCAGGGAGGCTGAGGCCGGAGAATCACTTGAACCCAGGAGGTGGAGGTT A C PNPLA3 Ensembl:ENSG00000100344 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1374721863 Functional Loss SNV dbSNP153 33..33 33 - - - 5469 RMVar_ID_5469 Human_SNP_ID_705239214 A-to-I Human chr22 + 43951215 43951215 43951215 CCTGTAATCCCAGCAACCAGGGAGGCTGAGGCAGGAGAATCACTTGAACCCAGGAGGTGGAGGTT CCTGTAATCCCAGCAACCAGGGAGGCTGAGGCGGGAGAATCACTTGAACCCAGGAGGTGGAGGTT A G PNPLA3 Ensembl:ENSG00000100344 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1374721863 Functional Loss SNV dbSNP153 33..33 33 - - - 5470 RMVar_ID_5470 Human_SNP_ID_705239222 A-to-I Human chr22 + 43951234 43951234 43951234 GGGAGGCTGAGGCAGGAGAATCACTTGAACCCAGGAGGTGGAGGTTGCAGTGACCCGAGATGCAG GGGAGGCTGAGGCAGGAGAATCACTTGAACCCGGGAGGTGGAGGTTGCAGTGACCCGAGATGCAG A G PNPLA3 Ensembl:ENSG00000100344 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1386239309 Functional Loss SNV dbSNP153 33..33 33 - - - 5471 RMVar_ID_5471 Human_SNP_ID_705277698 A-to-I Human chr22 + 44096795 44096795 44096795 CTGTCCTTGGGCACGTTTTATTGCAGCTGGCTATGACGCACAAGGTGGGGAGGGCGGGGGCTCGG CTGTCCTTGGGCACGTTTTATTGCAGCTGGCTGTGACGCACAAGGTGGGGAGGGCGGGGGCTCGG A G PARVB Ensembl:ENSG00000188677 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2299849 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_205,GWAS_ID_206 RMVar_hsa_circ_16447,RMVar_hsa_circ_214940,RMVar_hsa_circ_308836,RMVar_hsa_circ_310547,RMVar_hsa_circ_354388,RMVar_hsa_circ_46473,RMVar_hsa_circ_214938,RMVar_hsa_circ_214939 5472 RMVar_ID_5472 Human_SNP_ID_705296246 A-to-I Human chr22 + 44158899 44158899 44158899 GTCAGGGAGGCAGACAATGTAAGCTGGTGGCGACAGCCAGAGAAATAGCAGAAATGGGGCCAGTG GTCAGGGAGGCAGACAATGTAAGCTGGTGGCGGCAGCCAGAGAAATAGCAGAAATGGGGCCAGTG A G PARVB Ensembl:ENSG00000188677 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs139072 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_207,GWAS_ID_208,GWAS_ID_209 RMVar_hsa_circ_46473,RMVar_hsa_circ_50138,RMVar_hsa_circ_349207,RMVar_hsa_circ_214944,RMVar_hsa_circ_214946,RMVar_hsa_circ_273408 5473 RMVar_ID_5473 Human_SNP_ID_705299456 A-to-I Human chr22 + 44170126 44170126 44170126 AGGCTCAATTGATCCTCCCACCTCAGCCTCCCAAGTAGCGGGGACCACAAGTGCACACCACTAGG AGGCTCAATTGATCCTCCCACCTCAGCCTCCCGAGTAGCGGGGACCACAAGTGCACACCACTAGG A G PARVB Ensembl:ENSG00000188677 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1014565325 Functional Loss SNV dbSNP153 33..33 33 - - - 5474 RMVar_ID_5474 Human_SNP_ID_705299751 A-to-I Human chr22 + 44171218 44171218 44171218 GGATTGGGATTTGAAAAGAACAGAGCTTGGCCAGGTGCGGTGGCTCACGCCTGTAATCCCAGCAC GGATTGGGATTTGAAAAGAACAGAGCTTGGCCCGGTGCGGTGGCTCACGCCTGTAATCCCAGCAC A C PARVB Ensembl:ENSG00000188677 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1012478929 Functional Loss SNV dbSNP153 33..33 33 - - - 5475 RMVar_ID_5475 Human_SNP_ID_705299791 A-to-I Human chr22 + 44171415 44171415 44171415 TATTCGGGAGGCTGAGGCAGGAGAATTGCATGAACCCAGGAGGTGGAAGTTGCAGTGAGCTGAGA TATTCGGGAGGCTGAGGCAGGAGAATTGCATGGACCCAGGAGGTGGAAGTTGCAGTGAGCTGAGA A G PARVB Ensembl:ENSG00000188677 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968496317 Functional Loss SNV dbSNP153 33..33 33 - - - 5476 RMVar_ID_5476 Human_SNP_ID_705482165 A-to-I Human chr22 + 44812542 44812542 44812542 CCACGCCCGGCTAATTTTTGTATTTTTAGTGGAGACGGGTTTTCACCATGTTGGCCAGGATGGTC CCACGCCCGGCTAATTTTTGTATTTTTAGTGGCGACGGGTTTTCACCATGTTGGCCAGGATGGTC A C ARHGAP8,PRR5-ARHGAP8 Ensembl:ENSG00000241484,Ensembl:ENSG00000248405 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs557986702 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_214955,RMVar_hsa_circ_39488,RMVar_hsa_circ_66902,RMVar_hsa_circ_214954,RMVar_hsa_circ_296274,RMVar_hsa_circ_322684,RMVar_hsa_circ_303226 5477 RMVar_ID_5477 Human_SNP_ID_705487810 A-to-I Human chr22 + 44829102 44829102 44829102 CAAGACCAGCCTGGCCGGTATGGTGAAACCCTATCTCTACTAAAAATACAAAAAAAAAAAAAAAA CAAGACCAGCCTGGCCGGTATGGTGAAACCCTGTCTCTACTAAAAATACAAAAAAAAAAAAAAAA A G ARHGAP8,PRR5-ARHGAP8 Ensembl:ENSG00000241484,Ensembl:ENSG00000248405 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1456495502 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39488,RMVar_hsa_circ_214956,RMVar_hsa_circ_298778 5478 RMVar_ID_5478 Human_SNP_ID_705496679 A-to-I Human chr22 + 44855933 44855933 44855933 GGAAGCACGGTGTTGGCATCTGCTTGGCTTCCAGGGAGGCCTCAGGAAGCTTTCAATTATGACGG GGAAGCACGGTGTTGGCATCTGCTTGGCTTCCGGGGAGGCCTCAGGAAGCTTTCAATTATGACGG A G ARHGAP8,PRR5-ARHGAP8 Ensembl:ENSG00000241484,Ensembl:ENSG00000248405 Protein coding,Protein coding intron,intron GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 31158229,32596459 RNA-Seq:(High) rs985265879 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115898,RMVar_hsa_circ_214958 5479 RMVar_ID_5479 Human_SNP_ID_705496687 A-to-I Human chr22 + 44855959 44855959 44855959 GCTTCCAGGGAGGCCTCAGGAAGCTTTCAATTATGACGGAGGGCAAAGGAGGAGCAGGTGTCTCA GCTTCCAGGGAGGCCTCAGGAAGCTTTCAATTGTGACGGAGGGCAAAGGAGGAGCAGGTGTCTCA A G ARHGAP8,PRR5-ARHGAP8 Ensembl:ENSG00000241484,Ensembl:ENSG00000248405 Protein coding,Protein coding intron,intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1021752946 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14519114 RMVar_hsa_circ_115898,RMVar_hsa_circ_214958 5480 RMVar_ID_5480 Human_SNP_ID_705496721 A-to-I Human chr22 + 44856035 44856035 44856035 TGGGAGCAAGATGGGGTGAGGTCATGCCACACACTTAACCAGATCTCTTGAGAAATCACTCACTC TGGGAGCAAGATGGGGTGAGGTCATGCCACACCCTTAACCAGATCTCTTGAGAAATCACTCACTC A C ARHGAP8,PRR5-ARHGAP8 Ensembl:ENSG00000241484,Ensembl:ENSG00000248405 Protein coding,Protein coding intron,intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1569182949 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115898,RMVar_hsa_circ_214958 5481 RMVar_ID_5481 Human_SNP_ID_705498010 A-to-I Human chr22 + 44858462 44858462 44858462 CCATCTCGGCTCAGTGCAGCCTCTGTCTTCTGAGTTCAAGCAATTCTCCAGCTTCAGCCTCCCAT CCATCTCGGCTCAGTGCAGCCTCTGTCTTCTGCGTTCAAGCAATTCTCCAGCTTCAGCCTCCCAT A C ARHGAP8,PRR5-ARHGAP8 Ensembl:ENSG00000241484,Ensembl:ENSG00000248405 Protein coding,Protein coding intron,intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1304968151 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14519178 RMVar_hsa_circ_115898,RMVar_hsa_circ_214958 5482 RMVar_ID_5482 Human_SNP_ID_705498011 A-to-I Human chr22 + 44858462 44858462 44858462 CCATCTCGGCTCAGTGCAGCCTCTGTCTTCTGAGTTCAAGCAATTCTCCAGCTTCAGCCTCCCAT CCATCTCGGCTCAGTGCAGCCTCTGTCTTCTGGGTTCAAGCAATTCTCCAGCTTCAGCCTCCCAT A G ARHGAP8,PRR5-ARHGAP8 Ensembl:ENSG00000241484,Ensembl:ENSG00000248405 Protein coding,Protein coding intron,intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1304968151 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14519178 RMVar_hsa_circ_115898,RMVar_hsa_circ_214958 5483 RMVar_ID_5483 Human_SNP_ID_705498734 A-to-I Human chr22 + 44859447 44859447 44859447 TGCCATAATTGGAAGCCTCCTGAGGCTTCTCCAGAAGCTGAACAGGTGCTGGTGCCATGCTTGTA TGCCATAATTGGAAGCCTCCTGAGGCTTCTCCCGAAGCTGAACAGGTGCTGGTGCCATGCTTGTA A C ARHGAP8,PRR5-ARHGAP8 Ensembl:ENSG00000241484,Ensembl:ENSG00000248405 Protein coding,Protein coding intron,intron GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs536464765 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115898,RMVar_hsa_circ_214958 5484 RMVar_ID_5484 Human_SNP_ID_705498735 A-to-I Human chr22 + 44859447 44859447 44859447 TGCCATAATTGGAAGCCTCCTGAGGCTTCTCCAGAAGCTGAACAGGTGCTGGTGCCATGCTTGTA TGCCATAATTGGAAGCCTCCTGAGGCTTCTCCGGAAGCTGAACAGGTGCTGGTGCCATGCTTGTA A G ARHGAP8,PRR5-ARHGAP8 Ensembl:ENSG00000241484,Ensembl:ENSG00000248405 Protein coding,Protein coding intron,intron GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs536464765 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115898,RMVar_hsa_circ_214958 5485 RMVar_ID_5485 Human_SNP_ID_705584364 A-to-I Human chr22 - 45133623 45133623 45133623 CAGCTCACTGCAACCTCCTCCTGCTGGGTTCAAACGATTCTCCTGCCTCAGCCTCCTGAGTAGCT CAGCTCACTGCAACCTCCTCCTGCTGGGTTCAGACGATTCTCCTGCCTCAGCCTCCTGAGTAGCT T C NUP50-DT Ensembl:ENSG00000226328 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1440360986 Functional Loss SNV dbSNP153 33..33 33 - - - 5486 RMVar_ID_5486 Human_SNP_ID_705588958 A-to-I Human chr22 - 45151317 45151317 45151317 TTGTTTGCTAGAGTCTGGGTTGTGTCCCCCCAAAATTCATCTTTTGAAGTCCTAATCCCTGTACC TTGTTTGCTAGAGTCTGGGTTGTGTCCCCCCAGAATTCATCTTTTGAAGTCCTAATCCCTGTACC T C NUP50-DT Ensembl:ENSG00000226328 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1378422729 Functional Loss SNV dbSNP153 33..33 33 - - - 5487 RMVar_ID_5487 Human_SNP_ID_705590518 A-to-I Human chr22 - 45157169 45157169 45157169 TGTAGCAATGTAGCACAGACTGAGTGGTTTAAACAAAAGATTGATTTCCTCACCGTCCTGGAGTC TGTAGCAATGTAGCACAGACTGAGTGGTTTAATCAAAAGATTGATTTCCTCACCGTCCTGGAGTC T A NUP50-DT Ensembl:ENSG00000226328 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1162584364 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1101930 5488 RMVar_ID_5488 Human_SNP_ID_705592193 A-to-I Human chr22 - 45162992 45162992 45162992 TTATATTTTTAGTAGAGACGGGTTTTCACCATATTGGTCAGGCTGGTCTCGAACTCGTGACCTCA TTATATTTTTAGTAGAGACGGGTTTTCACCATGTTGGTCAGGCTGGTCTCGAACTCGTGACCTCA T C NUP50-DT Ensembl:ENSG00000226328 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs189661763 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14519495 5489 RMVar_ID_5489 Human_SNP_ID_705592216 A-to-I Human chr22 - 45163055 45163055 45163055 CTCCTGCCTCAGCCTCCCGAGTAGTTGGGATTACAGTCGTGCGCCACCACGCCCGGCTAATGTTT CTCCTGCCTCAGCCTCCCGAGTAGTTGGGATTCCAGTCGTGCGCCACCACGCCCGGCTAATGTTT T G NUP50-DT Ensembl:ENSG00000226328 lincRNA intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1271137470 Functional Loss SNV dbSNP153 33..33 33 - - - 5490 RMVar_ID_5490 Human_SNP_ID_705592219 A-to-I Human chr22 - 45163065 45163065 45163065 TCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGTTGGGATTACAGTCGTGCGCCACCACGCCCG TCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTGGTTGGGATTACAGTCGTGCGCCACCACGCCCG T C NUP50-DT Ensembl:ENSG00000226328 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1014348495 Functional Loss SNV dbSNP153 33..33 33 - - - 5491 RMVar_ID_5491 Human_SNP_ID_705592234 A-to-I Human chr22 - 45163114 45163114 45163114 GGAGTGAAGTGGCACGATCTTGGCCTACTGCAACCTCTGCCTCCCGGATTCAAGCGATTCTCCTG GGAGTGAAGTGGCACGATCTTGGCCTACTGCAGCCTCTGCCTCCCGGATTCAAGCGATTCTCCTG T C NUP50-DT Ensembl:ENSG00000226328 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs530886757 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14519496 5492 RMVar_ID_5492 Human_SNP_ID_705596685 A-to-I Human chr22 + 45176883 45176883 45176883 CCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCATGCACCACCATGCCCAGCTAATTTTTGT CCTGCCTCAGCCTCCCGAGTAGCTGGGACTACGGGCATGCACCACCATGCCCAGCTAATTTTTGT A G NUP50 Ensembl:ENSG00000093000 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs890480679 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58728,RMVar_hsa_circ_336326 5493 RMVar_ID_5493 Human_SNP_ID_705596997 A-to-I Human chr22 + 45177965 45177964 45177965 CCTGGCCAACATGACGAAACCCCATCTCTACTAAAATACAAAAATTAGCCGGGTGTGGTGGCGGG CCTGGCCAACATGACGAAACCCCATCTCTACT_AAATACAAAAATTAGCCGGGTGTGGTGGCGGG TA T NUP50 Ensembl:ENSG00000093000 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs71315127 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_58728,RMVar_hsa_circ_336326 5494 RMVar_ID_5494 Human_SNP_ID_705597020 A-to-I Human chr22 + 45178015 45178015 45178015 GGGTGTGGTGGCGGGTGCCCGTAATCCCACCTACTCGGGAGGTTGAGGCAGGAGAATCGCTTGAA GGGTGTGGTGGCGGGTGCCCGTAATCCCACCTGCTCGGGAGGTTGAGGCAGGAGAATCGCTTGAA A G NUP50 Ensembl:ENSG00000093000 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1026372662 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58728,RMVar_hsa_circ_336326 5495 RMVar_ID_5495 Human_SNP_ID_705597576 A-to-I Human chr22 + 45179675 45179675 45179675 GGGAGGCCAAAGTGGAAGGCTCACCTGAGGCCAGGAGTTTGAGACCAGCCTGGGCAACATAGCAA GGGAGGCCAAAGTGGAAGGCTCACCTGAGGCCGGGAGTTTGAGACCAGCCTGGGCAACATAGCAA A G NUP50 Ensembl:ENSG00000093000 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1171424712 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58728,RMVar_hsa_circ_342491 5496 RMVar_ID_5496 Human_SNP_ID_705598409 A-to-I Human chr22 + 45182337 45182334 45182337 GTGGCGCACGCCTGTAATCCCAGCTGTTTGGGAGGCTGAGGCATGAGAATTGCTTGAACCCTGAG GTGGCGCACGCCTGTAATCCCAGCTGTTTG___GGCTGAGGCATGAGAATTGCTTGAACCCTGAG GGGA G NUP50 Ensembl:ENSG00000093000 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1437324197 Functional Loss DEL dbSNP153 31..33 33 - - - 5497 RMVar_ID_5497 Human_SNP_ID_705598410 A-to-I Human chr22 + 45182337 45182337 45182337 GTGGCGCACGCCTGTAATCCCAGCTGTTTGGGAGGCTGAGGCATGAGAATTGCTTGAACCCTGAG GTGGCGCACGCCTGTAATCCCAGCTGTTTGGGGGGCTGAGGCATGAGAATTGCTTGAACCCTGAG A G NUP50 Ensembl:ENSG00000093000 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1456346373 Functional Loss SNV dbSNP153 33..33 33 - - - 5498 RMVar_ID_5498 Human_SNP_ID_705598420 A-to-I Human chr22 + 45182374 45182374 45182374 GAGGCATGAGAATTGCTTGAACCCTGAGAAGCAGAGGTTGCAGTGAGCCAAGATCATGCCACTGC GAGGCATGAGAATTGCTTGAACCCTGAGAAGCGGAGGTTGCAGTGAGCCAAGATCATGCCACTGC A G NUP50 Ensembl:ENSG00000093000 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs140678899 Functional Loss SNV dbSNP153 33..33 33 - - - 5499 RMVar_ID_5499 Human_SNP_ID_705602571 A-to-I Human chr22 - 45194408 45194408 45194408 TAAGACCTTAGGTTTCCTCAGCGGAAAACTGTACTTTAATCCCAAACCCCCTTTAAGACATATTG TAAGACCTTAGGTTTCCTCAGCGGAAAACTGTTCTTTAATCCCAAACCCCCTTTAAGACATATTG T A KIAA0930 Ensembl:ENSG00000100364 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs112115936 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17702251,Human_RBP_ID_17988223 RMVar_hsa_circ_78864,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_214968,RMVar_hsa_circ_76949,RMVar_hsa_circ_214969,RMVar_hsa_circ_214967,RMVar_hsa_circ_214964,RMVar_hsa_circ_214965,RMVar_hsa_circ_214963,RMVar_hsa_circ_214961 5500 RMVar_ID_5500 Human_SNP_ID_705602572 A-to-I Human chr22 - 45194408 45194408 45194408 TAAGACCTTAGGTTTCCTCAGCGGAAAACTGTACTTTAATCCCAAACCCCCTTTAAGACATATTG TAAGACCTTAGGTTTCCTCAGCGGAAAACTGTGCTTTAATCCCAAACCCCCTTTAAGACATATTG T C KIAA0930 Ensembl:ENSG00000100364 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs112115936 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17702251,Human_RBP_ID_17988223 RMVar_hsa_circ_78864,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_214968,RMVar_hsa_circ_76949,RMVar_hsa_circ_214969,RMVar_hsa_circ_214967,RMVar_hsa_circ_214964,RMVar_hsa_circ_214965,RMVar_hsa_circ_214963,RMVar_hsa_circ_214961 5501 RMVar_ID_5501 Human_SNP_ID_705602574 A-to-I Human chr22 - 45194413 45194413 45194413 CCCTTTAAGACCTTAGGTTTCCTCAGCGGAAAACTGTACTTTAATCCCAAACCCCCTTTAAGACA CCCTTTAAGACCTTAGGTTTCCTCAGCGGAAAGCTGTACTTTAATCCCAAACCCCCTTTAAGACA T C KIAA0930 Ensembl:ENSG00000100364 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs112207040 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27495358 RMVar_hsa_circ_78864,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_214968,RMVar_hsa_circ_76949,RMVar_hsa_circ_214969,RMVar_hsa_circ_214967,RMVar_hsa_circ_214964,RMVar_hsa_circ_214965,RMVar_hsa_circ_214963,RMVar_hsa_circ_214961 5502 RMVar_ID_5502 Human_SNP_ID_705602591 A-to-I Human chr22 - 45194478 45194478 45194478 AATGCGGGGAAGACTAATGCATGGTGACACCTAGTTTTCCTCAACAGGACACTTGATCCCAAAAC AATGCGGGGAAGACTAATGCATGGTGACACCTCGTTTTCCTCAACAGGACACTTGATCCCAAAAC T G KIAA0930 Ensembl:ENSG00000100364 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1285281293 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_582687,Human_RBP_ID_2721787,Human_RBP_ID_17988224 RMVar_hsa_circ_78864,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_214968,RMVar_hsa_circ_76949,RMVar_hsa_circ_214969,RMVar_hsa_circ_214967,RMVar_hsa_circ_214964,RMVar_hsa_circ_214965,RMVar_hsa_circ_214963,RMVar_hsa_circ_214961 5503 RMVar_ID_5503 Human_SNP_ID_705604551 A-to-I Human chr22 - 45200430 45200430 45200430 TAGTTTCCCCATGTGTCAGATGGGCTGACGCTAGCCCCTGTCTCACGGAGCTGGAGGCTCAGAGG TAGTTTCCCCATGTGTCAGATGGGCTGACGCTGGCCCCTGTCTCACGGAGCTGGAGGCTCAGAGG T C KIAA0930 Ensembl:ENSG00000100364 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1233705081 Functional Loss SNV dbSNP153 33..33 33 - - - 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 5504 RMVar_ID_5504 Human_SNP_ID_705640560 A-to-I Human chr22 + 45317354 45317354 45317354 CAAGCCGAGATTGCGCCATTGCACTCTAGCCTAGGCAACAAGAGTGAAACTCACTCTCAAAACAC CAAGCCGAGATTGCGCCATTGCACTCTAGCCTGGGCAACAAGAGTGAAACTCACTCTCAAAACAC A G FAM118A Ensembl:ENSG00000100376 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1393660329 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_214974,RMVar_hsa_circ_374596 5505 RMVar_ID_5505 Human_SNP_ID_705645004 A-to-I Human chr22 + 45332923 45332923 45332923 GCGCCACCATGCCTGGCTAATTTTGTATTTTTAGTAGAGATAGGGTTTCACCATGTTGGTCAGGC GCGCCACCATGCCTGGCTAATTTTGTATTTTTGGTAGAGATAGGGTTTCACCATGTTGGTCAGGC A G FAM118A Ensembl:ENSG00000100376 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs910575512 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56853,RMVar_hsa_circ_68942,RMVar_hsa_circ_214978,RMVar_hsa_circ_93063,RMVar_hsa_circ_214979,RMVar_hsa_circ_347303 5506 RMVar_ID_5506 Human_SNP_ID_705645086 A-to-I Human chr22 + 45333237 45333237 45333237 CTAGTGACAGTCTGTAACTAGAACTTTAAAGTAACTTCAGGCTGGGCACCGTGGCTCACGCCTGT CTAGTGACAGTCTGTAACTAGAACTTTAAAGTGACTTCAGGCTGGGCACCGTGGCTCACGCCTGT A G FAM118A Ensembl:ENSG00000100376 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1211556564 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21896860 RMVar_hsa_circ_56853,RMVar_hsa_circ_68942,RMVar_hsa_circ_214978,RMVar_hsa_circ_93063,RMVar_hsa_circ_214979,RMVar_hsa_circ_347303 5507 RMVar_ID_5507 Human_SNP_ID_705645605 A-to-I Human chr22 + 45335169 45335169 45335169 TTTGCCAGCTGGCTCCTTCAGCGAGTCCTCGCACCAAGCCTGGGAGGTAGAGGTGAGGGCAGCGA TTTGCCAGCTGGCTCCTTCAGCGAGTCCTCGCGCCAAGCCTGGGAGGTAGAGGTGAGGGCAGCGA A G FAM118A Ensembl:ENSG00000100376 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2350629 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22086649,Human_RBP_ID_22550841,Human_RBP_ID_22674444 Human_Splice_Rec_2175319 GWAS_ID_210,GWAS_ID_211,GWAS_ID_212,GWAS_ID_213,GWAS_ID_214 RMVar_hsa_circ_56853,RMVar_hsa_circ_68942,RMVar_hsa_circ_214978,RMVar_hsa_circ_93063,RMVar_hsa_circ_214979,RMVar_hsa_circ_347303 5508 RMVar_ID_5508 Human_SNP_ID_705645606 A-to-I Human chr22 + 45335169 45335169 45335169 TTTGCCAGCTGGCTCCTTCAGCGAGTCCTCGCACCAAGCCTGGGAGGTAGAGGTGAGGGCAGCGA TTTGCCAGCTGGCTCCTTCAGCGAGTCCTCGCTCCAAGCCTGGGAGGTAGAGGTGAGGGCAGCGA A T FAM118A Ensembl:ENSG00000100376 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2350629 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22086649,Human_RBP_ID_22550841,Human_RBP_ID_22674444 Human_Splice_Rec_2175319 GWAS_ID_210,GWAS_ID_211,GWAS_ID_212,GWAS_ID_213,GWAS_ID_214 RMVar_hsa_circ_56853,RMVar_hsa_circ_68942,RMVar_hsa_circ_214978,RMVar_hsa_circ_93063,RMVar_hsa_circ_214979,RMVar_hsa_circ_347303 5509 RMVar_ID_5509 Human_SNP_ID_705647319 A-to-I Human chr22 + 45340983 45340983 45340983 CACCACCATGCCCAGCTAATTTTTTTATTTTTAGTAGAGTTGGAGTTTCACCATGTTGGCCAGGA CACCACCATGCCCAGCTAATTTTTTTATTTTTCGTAGAGTTGGAGTTTCACCATGTTGGCCAGGA A C FAM118A Ensembl:ENSG00000100376 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1480049560 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14520479 RMVar_hsa_circ_93063,RMVar_hsa_circ_214979 5510 RMVar_ID_5510 Human_SNP_ID_705647334 A-to-I Human chr22 + 45341037 45341036 45341037 GTTGGCCAGGATGGTCTCGAACTCTTGACCTCAGGTGATCCACCCGCCTTGGCCTCCCAAAGTGC GTTGGCCAGGATGGTCTCGAACTCTTGACCTC_GGTGATCCACCCGCCTTGGCCTCCCAAAGTGC CA C FAM118A Ensembl:ENSG00000100376 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1450413736 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_93063,RMVar_hsa_circ_214979 5511 RMVar_ID_5511 Human_SNP_ID_705647335 A-to-I Human chr22 + 45341037 45341037 45341037 GTTGGCCAGGATGGTCTCGAACTCTTGACCTCAGGTGATCCACCCGCCTTGGCCTCCCAAAGTGC GTTGGCCAGGATGGTCTCGAACTCTTGACCTCGGGTGATCCACCCGCCTTGGCCTCCCAAAGTGC A G FAM118A Ensembl:ENSG00000100376 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs763647872 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93063,RMVar_hsa_circ_214979 5512 RMVar_ID_5512 Human_SNP_ID_705647344 A-to-I Human chr22 + 45341071 45341071 45341071 GTGATCCACCCGCCTTGGCCTCCCAAAGTGCTAGGATTACAGGCATGAGCCACTGCGCCCAGCAA GTGATCCACCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGCGCCCAGCAA A G FAM118A Ensembl:ENSG00000100376 Protein coding 3'UTR GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs941398673 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93063,RMVar_hsa_circ_214979 5513 RMVar_ID_5513 Human_SNP_ID_705693483 A-to-I Human chr22 + 45519914 45519913 45519914 GAGATCACCCGGGCGCGGTGGCTCACCCCTGTAATCCCAGCACTTTGGGAGACCAAGGCGGGTGG GAGATCACCCGGGCGCGGTGGCTCACCCCTGT_ATCCCAGCACTTTGGGAGACCAAGGCGGGTGG TA T FBLN1 Ensembl:ENSG00000077942 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1293691344 Functional Loss DEL 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_214984,RMVar_hsa_circ_214985 5514 RMVar_ID_5514 Human_SNP_ID_705694398 A-to-I Human chr22 + 45523619 45523619 45523619 CCAGCTGCCGGTGAGGCTGAGGCAGGAGAATCACTTGAACCCAGGAAGCGGAGGTTGCAGTGAGC CCAGCTGCCGGTGAGGCTGAGGCAGGAGAATCGCTTGAACCCAGGAAGCGGAGGTTGCAGTGAGC A G FBLN1 Ensembl:ENSG00000077942 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1016309835 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 5515 RMVar_ID_5515 Human_SNP_ID_705715855 A-to-I Human chr22 + 45599734 45599734 45599734 GAGGTCAGGAGTTTGAGACTAGCCTGATCAACATGGAGAAACCCCGTCTCTACTAAAAATATAAA GAGGTCAGGAGTTTGAGACTAGCCTGATCAACGTGGAGAAACCCCGTCTCTACTAAAAATATAAA A G FBLN1 Ensembl:ENSG00000077942 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs574088912 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107083,RMVar_hsa_circ_214990,RMVar_hsa_circ_111789,RMVar_hsa_circ_215004,RMVar_hsa_circ_91015,RMVar_hsa_circ_215006 5516 RMVar_ID_5516 Human_SNP_ID_705717904 A-to-I Human chr22 + 45606411 45606411 45606411 ACTGGGCCCGTTAGTCTTTGCTCCCTGATACTATCTGATACCATCTGGTCTCACTCCTTCCTTCC ACTGGGCCCGTTAGTCTTTGCTCCCTGATACTGTCTGATACCATCTGGTCTCACTCCTTCCTTCC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1387683259 Functional Loss SNV dbSNP153 33..33 33 - - - 5517 RMVar_ID_5517 Human_SNP_ID_705730613 A-to-I Human chr22 + 45655131 45655131 45655131 CTCACTATAACCTCAAACTCCTGGGCTCAAGCAATTCTATTGCCCCAGCTTCCTGAATAGCTGGG CTCACTATAACCTCAAACTCCTGGGCTCAAGCTATTCTATTGCCCCAGCTTCCTGAATAGCTGGG A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1389593982 Functional Loss SNV dbSNP153 33..33 33 - - - 5518 RMVar_ID_5518 Human_SNP_ID_705740426 A-to-I Human chr22 + 45695633 45695633 45695633 CTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCGCCTGCCGCCGCACTCGGCTGATTTTT CTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTGCAGGCGCCTGCCGCCGCACTCGGCTGATTTTT A G ATXN10 Ensembl:ENSG00000130638 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1416157634 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_215016,RMVar_hsa_circ_97228,RMVar_hsa_circ_84094,RMVar_hsa_circ_106749,RMVar_hsa_circ_119628,RMVar_hsa_circ_215009,RMVar_hsa_circ_215010,RMVar_hsa_circ_113082,RMVar_hsa_circ_270513,RMVar_hsa_circ_215011,RMVar_hsa_circ_215012,RMVar_hsa_circ_215013,RMVar_hsa_circ_323566,RMVar_hsa_circ_315440,RMVar_hsa_circ_274330,RMVar_hsa_circ_281487,RMVar_hsa_circ_273382,RMVar_hsa_circ_215017,RMVar_hsa_circ_215022,RMVar_hsa_circ_215014,RMVar_hsa_circ_215015,RMVar_hsa_circ_278539,RMVar_hsa_circ_283692,RMVar_hsa_circ_315660,RMVar_hsa_circ_278740,RMVar_hsa_circ_215023,RMVar_hsa_circ_215020,RMVar_hsa_circ_215021 5519 RMVar_ID_5519 Human_SNP_ID_705749068 A-to-I Human chr22 + 45730457 45730457 45730457 CATTTAGGTTGTTTGTTTGTTTGTTTTGAGACAAAGCCTTGCTCTGTCGCCCAAGCTGGAGCACA CATTTAGGTTGTTTGTTTGTTTGTTTTGAGACGAAGCCTTGCTCTGTCGCCCAAGCTGGAGCACA A G ATXN10 Ensembl:ENSG00000130638 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1177707795 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113082,RMVar_hsa_circ_270513,RMVar_hsa_circ_215013,RMVar_hsa_circ_315440,RMVar_hsa_circ_215024,RMVar_hsa_circ_28976,RMVar_hsa_circ_215014,RMVar_hsa_circ_278740,RMVar_hsa_circ_215023,RMVar_hsa_circ_275917,RMVar_hsa_circ_108537,RMVar_hsa_circ_215025,RMVar_hsa_circ_324029,RMVar_hsa_circ_215031,RMVar_hsa_circ_215034,RMVar_hsa_circ_270309,RMVar_hsa_circ_351949,RMVar_hsa_circ_215035 5520 RMVar_ID_5520 Human_SNP_ID_705749093 A-to-I Human chr22 + 45730560 45730560 45730560 GGTTCAGTCAATTCTCCTGTCTTGGCTACCCAAATAACTGGGATTATAGGTGCACACCACCACCA GGTTCAGTCAATTCTCCTGTCTTGGCTACCCAGATAACTGGGATTATAGGTGCACACCACCACCA A G ATXN10 Ensembl:ENSG00000130638 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1382799325 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113082,RMVar_hsa_circ_270513,RMVar_hsa_circ_215013,RMVar_hsa_circ_315440,RMVar_hsa_circ_215024,RMVar_hsa_circ_28976,RMVar_hsa_circ_215014,RMVar_hsa_circ_278740,RMVar_hsa_circ_215023,RMVar_hsa_circ_275917,RMVar_hsa_circ_108537,RMVar_hsa_circ_215025,RMVar_hsa_circ_324029,RMVar_hsa_circ_215031,RMVar_hsa_circ_215034,RMVar_hsa_circ_270309,RMVar_hsa_circ_351949,RMVar_hsa_circ_215035 5521 RMVar_ID_5521 Human_SNP_ID_705755604 A-to-I Human chr22 + 45754744 45754744 45754744 AGATATGGTGGCTCATGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGGATCGCTTGAA AGATATGGTGGCTCATGCCTGTAGTCCCAGCTGCTTGGGAGGCTGAGGCAGGAGGATCGCTTGAA A G ATXN10 Ensembl:ENSG00000130638 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1382180551 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25677864 RMVar_hsa_circ_215024,RMVar_hsa_circ_108537,RMVar_hsa_circ_90837,RMVar_hsa_circ_215038 5522 RMVar_ID_5522 Human_SNP_ID_705755944 A-to-I Human chr22 + 45756169 45756169 45756169 TTTACCTAGACTTTTTTTTTTTTTAAAGAGACAAGGTTGTGCTTTCTCACCCAGGCTGGAGTGCA TTTACCTAGACTTTTTTTTTTTTTAAAGAGACGAGGTTGTGCTTTCTCACCCAGGCTGGAGTGCA A G ATXN10 Ensembl:ENSG00000130638 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs943609276 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14521325 RMVar_hsa_circ_215024,RMVar_hsa_circ_108537,RMVar_hsa_circ_90837,RMVar_hsa_circ_215038 5523 RMVar_ID_5523 Human_SNP_ID_705868586 A-to-I Human chr22 + 46152975 46152975 46152975 GGGCATGGTGGCGGACATCTGTAATCCCAGCTACTCAAGAAACTGAGGCAGGAGAATCGCTTGAG GGGCATGGTGGCGGACATCTGTAATCCCAGCTTCTCAAGAAACTGAGGCAGGAGAATCGCTTGAG A T PPARA Ensembl:ENSG00000186951 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1292124147 Functional Loss SNV dbSNP153 33..33 33 - - - 5524 RMVar_ID_5524 Human_SNP_ID_705888440 A-to-I Human chr22 + 46228415 46228415 46228415 AAATTAACCAGGCGTGGTTGGTGGGTGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA AAATTAACCAGGCGTGGTTGGTGGGTGCCTGTGATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA A G PPARA Ensembl:ENSG00000186951 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1003473799 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_364721,RMVar_hsa_circ_69600 5525 RMVar_ID_5525 Human_SNP_ID_705891039 A-to-I Human chr22 + 46239502 46239502 46239502 TGCCCACACACAGGGGAGCAGCATCTCGTATGACGTCTGGAAGGAACTTCGGTTGTGTAAAGGGA TGCCCACACACAGGGGAGCAGCATCTCGTATGCCGTCTGGAAGGAACTTCGGTTGTGTAAAGGGA A C PPARA Ensembl:ENSG00000186951 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs945998743 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23952783 Human_miRNA_ID_1392518 5526 RMVar_ID_5526 Human_SNP_ID_705906100 A-to-I Human chr22 + 46292253 46292253 46292253 TCATCCAGGTTGGAATGCAGTGGTGTGATCACAGTTCACTGTAAACTCAAACTCCTGGGCTCAAG TCATCCAGGTTGGAATGCAGTGGTGTGATCACTGTTCACTGTAAACTCAAACTCCTGGGCTCAAG A T TTC38 Ensembl:ENSG00000075234 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 29129909,30559470 RNA-Seq:(High) rs1474656697 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18791573,Human_RBP_ID_25680532 Human_Splice_Rec_2176080,Human_Splice_Rec_2176081 RMVar_hsa_circ_87203,RMVar_hsa_circ_215072,RMVar_hsa_circ_103456,RMVar_hsa_circ_215074,RMVar_hsa_circ_110881,RMVar_hsa_circ_215078 5527 RMVar_ID_5527 Human_SNP_ID_705909504 A-to-I Human chr22 + 46304792 46304792 46304792 CTTGTTCCCAGCAGTTTGAGACCAGCCTGGGCAACATGAGGAGATCCCATCTCTACAAAAAATAC CTTGTTCCCAGCAGTTTGAGACCAGCCTGGGCGACATGAGGAGATCCCATCTCTACAAAAAATAC A G GTSE1 Ensembl:ENSG00000075218 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560552159 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25509,RMVar_hsa_circ_215081 5528 RMVar_ID_5528 Human_SNP_ID_705911615 A-to-I Human chr22 + 46312532 46312532 46312532 ATGGTGGTGAGCAACGGCAGTCCCAGCTACTCAGGAGGCTGAGGTGGGATGATTGCTTGAGCCCA ATGGTGGTGAGCAACGGCAGTCCCAGCTACTCGGGAGGCTGAGGTGGGATGATTGCTTGAGCCCA A G GTSE1 Ensembl:ENSG00000075218 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1045965547 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6108,RMVar_hsa_circ_344587,RMVar_hsa_circ_25509,RMVar_hsa_circ_215081,RMVar_hsa_circ_336903,RMVar_hsa_circ_341430,RMVar_hsa_circ_215083,RMVar_hsa_circ_66120,RMVar_hsa_circ_327277,RMVar_hsa_circ_19640,RMVar_hsa_circ_215084 5529 RMVar_ID_5529 Human_SNP_ID_705917398 A-to-I Human chr22 + 46333558 46333558 46333558 CAGACAGAACCAGTGTACATCTTACACGTATTAATTGATGTCCTGTGTCTCCCTAATATGTATCA CAGACAGAACCAGTGTACATCTTACACGTATTTATTGATGTCCTGTGTCTCCCTAATATGTATCA A T TRMU Ensembl:ENSG00000100416 Protein coding exon GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1001559228 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1613602,Human_RBP_ID_2723885,Human_RBP_ID_3675118,Human_RBP_ID_8552781,Human_RBP_ID_17515719,Human_RBP_ID_18791617,Human_RBP_ID_27495521 Human_miRNA_ID_2627947,Human_miRNA_ID_2748783 RMVar_hsa_circ_215088,RMVar_hsa_circ_92961 5530 RMVar_ID_5530 Human_SNP_ID_705917533 A-to-I Human chr22 + 46334072 46334072 46334072 CCGAGGCGGGCGGATCACAAGGTCAGGAGATCAAGACCATCCTGGCCAACATGGTGAAATGCCGT CCGAGGCGGGCGGATCACAAGGTCAGGAGATCGAGACCATCCTGGCCAACATGGTGAAATGCCGT A G TRMU Ensembl:ENSG00000100416 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417340380 Functional Loss SNV dbSNP153 33..33 33 - - - 5531 RMVar_ID_5531 Human_SNP_ID_705984694 A-to-I Human chr22 - 46544268 46544268 46544268 TGTTTTTAGTGGAGACAGGGTTTCGCCGTGTTAGCCAGGATGGTCTCCATCTCCTGACCTCATGA TGTTTTTAGTGGAGACAGGGTTTCGCCGTGTTCGCCAGGATGGTCTCCATCTCCTGACCTCATGA T G lnc-CDPF1-1,RF00017-124 RNACentral:URS0000D58ABB,RNACentral:URS000099C5B7 lincRNA,SRP RNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1312747045 Functional Loss SNV dbSNP153 33..33 33 - - - 5532 RMVar_ID_5532 Human_SNP_ID_706027911 A-to-I Human chr22 - 46685158 46685154 46685158 GCTGAGGCAGGAGAATCGCTTGAACCCAAGAAAGAGGTGGAGGTTGCGGTGAGCCAAGATTGCGC GCTGAGGCAGGAGAATCGCTTGAACCCAAGAA____GTGGAGGTTGCGGTGAGCCAAGATTGCGC CCTCT C CERK Ensembl:ENSG00000100422 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1463365962 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_268955 5533 RMVar_ID_5533 Human_SNP_ID_706027912 A-to-I Human chr22 - 46685158 46685155 46685159 GCTGAGGCAGGAGAATCGCTTGAACCCAAGAAAGAGGTGGAGGTTGCGGTGAGCCAAGATTGCGC GCTGAGGCAGGAGAATCGCTTGAACCCAAGA____GGTGGAGGTTGCGGTGAGCCAAGATTGCGC CTCTT C CERK Ensembl:ENSG00000100422 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs3830883 Functional Loss DEL dbSNP153 32..35 33 - - - GWAS_ID_215,GWAS_ID_216,GWAS_ID_217,GWAS_ID_218,GWAS_ID_219,GWAS_ID_220,GWAS_ID_221 RMVar_hsa_circ_268955 5534 RMVar_ID_5534 Human_SNP_ID_706031951 A-to-I Human chr22 - 46698860 46698860 46698860 GTCTTCCTCCGTCACTCAGGCTGGAGTGCAGTAGCACGATCACGGTTCACTGCAGCCTTGACCTC GTCTTCCTCCGTCACTCAGGCTGGAGTGCAGTGGCACGATCACGGTTCACTGCAGCCTTGACCTC T C CERK Ensembl:ENSG00000100422 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1315405674 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4825,RMVar_hsa_circ_18547,RMVar_hsa_circ_370003,RMVar_hsa_circ_268955,RMVar_hsa_circ_78712,RMVar_hsa_circ_215134,RMVar_hsa_circ_215135,RMVar_hsa_circ_331037,RMVar_hsa_circ_338545,RMVar_hsa_circ_299894,RMVar_hsa_circ_85837,RMVar_hsa_circ_215136,RMVar_hsa_circ_215137,RMVar_hsa_circ_25482,RMVar_hsa_circ_266429,RMVar_hsa_circ_215138,RMVar_hsa_circ_719 5535 RMVar_ID_5535 Human_SNP_ID_706036327 A-to-I Human chr22 - 46713688 46713688 46713688 TGTTTTCACATTGATTCATGTTGGTCGCACCCAGTAGTTTGCTTATTTCATGACTGAAGGATGCT TGTTTTCACATTGATTCATGTTGGTCGCACCCGGTAGTTTGCTTATTTCATGACTGAAGGATGCT T C CERK Ensembl:ENSG00000100422 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs135703 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14523914,Human_RBP_ID_17147649 GWAS_ID_222 RMVar_hsa_circ_18547,RMVar_hsa_circ_268955,RMVar_hsa_circ_25482,RMVar_hsa_circ_330381,RMVar_hsa_circ_719,RMVar_hsa_circ_127219,RMVar_hsa_circ_334074,RMVar_hsa_circ_344224,RMVar_hsa_circ_215144,RMVar_hsa_circ_215145 5536 RMVar_ID_5536 Human_SNP_ID_706036340 A-to-I Human chr22 - 46713724 46713724 46713724 TGCTCCTGGGTGGAAGCCTCCAGTCTCTCTGCATACTGTTTTCACATTGATTCATGTTGGTCGCA TGCTCCTGGGTGGAAGCCTCCAGTCTCTCTGCGTACTGTTTTCACATTGATTCATGTTGGTCGCA T C CERK Ensembl:ENSG00000100422 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs13054785 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_223,GWAS_ID_224,GWAS_ID_225,GWAS_ID_226 RMVar_hsa_circ_18547,RMVar_hsa_circ_268955,RMVar_hsa_circ_25482,RMVar_hsa_circ_330381,RMVar_hsa_circ_719,RMVar_hsa_circ_127219,RMVar_hsa_circ_334074,RMVar_hsa_circ_344224,RMVar_hsa_circ_215144,RMVar_hsa_circ_215145 5537 RMVar_ID_5537 Human_SNP_ID_706037016 A-to-I Human chr22 - 46716721 46716721 46716721 TTGGCCAGGCTGATCTTGAACTCTTGGCCTCAAGTGATCTACCTGCCTCAGCCTCCCAAAGTGCT TTGGCCAGGCTGATCTTGAACTCTTGGCCTCAGGTGATCTACCTGCCTCAGCCTCCCAAAGTGCT T C CERK Ensembl:ENSG00000100422 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs983667263 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18547,RMVar_hsa_circ_268955,RMVar_hsa_circ_25482,RMVar_hsa_circ_330381,RMVar_hsa_circ_719,RMVar_hsa_circ_127219,RMVar_hsa_circ_334074,RMVar_hsa_circ_344224,RMVar_hsa_circ_215144,RMVar_hsa_circ_215145 5538 RMVar_ID_5538 Human_SNP_ID_706062488 A-to-I Human chr22 + 46807834 46807834 46807834 TTTTAGAAATTTTATACAGGGCCAGGTGAAGTAGCTCATACTTGTAATCCCAGCAGTTGGGAGGC TTTTAGAAATTTTATACAGGGCCAGGTGAAGTGGCTCATACTTGTAATCCCAGCAGTTGGGAGGC A G TBC1D22A Ensembl:ENSG00000054611 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs780817007 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17208601 RMVar_hsa_circ_50769,RMVar_hsa_circ_8138,RMVar_hsa_circ_333121,RMVar_hsa_circ_331055,RMVar_hsa_circ_271069,RMVar_hsa_circ_53449 5539 RMVar_ID_5539 Human_SNP_ID_706149444 A-to-I Human chr22 + 47119680 47119680 47119680 CAGCACGCCCGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACTATGTTGGCCAGGCTGG CAGCACGCCCGGCTAATTTTTGTATTTTTAGTGGAGACAGGGTTTCACTATGTTGGCCAGGCTGG A G TBC1D22A Ensembl:ENSG00000054611 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs944055004 Functional Loss SNV dbSNP153 33..33 33 - - - 5540 RMVar_ID_5540 Human_SNP_ID_706166239 A-to-I Human chr22 + 47174625 47174624 47174626 TGTGACTGGTTCCATCATGGACCGGTTCCTCCATGGACCGGTTCCTCCGTGGACCGGTTCCGCCA TGTGACTGGTTCCATCATGGACCGGTTCCTCC__GGACCGGTTCCTCCGTGGACCGGTTCCGCCA CAT C TBC1D22A Ensembl:ENSG00000054611 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1321981179 Functional Loss DEL dbSNP153 33..34 33 - - - 5541 RMVar_ID_5541 Human_SNP_ID_706166240 A-to-I Human chr22 + 47174625 47174625 47174625 TGTGACTGGTTCCATCATGGACCGGTTCCTCCATGGACCGGTTCCTCCGTGGACCGGTTCCGCCA TGTGACTGGTTCCATCATGGACCGGTTCCTCCGTGGACCGGTTCCTCCGTGGACCGGTTCCGCCA A G TBC1D22A Ensembl:ENSG00000054611 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs56869004 Functional Loss SNV dbSNP153 33..33 33 - - - 5542 RMVar_ID_5542 Human_SNP_ID_706947125 A-to-I Human chr22 - 49806075 49806075 49806075 CGAGACCAGCCTGGCCAACATAGCAAAACCCCATCTTCACTGAAAACATAAAAATTAGCTGGGTG CGAGACCAGCCTGGCCAACATAGCAAAACCCCTTCTTCACTGAAAACATAAAAATTAGCTGGGTG T A BRD1 Ensembl:ENSG00000100425 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs901459433 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265202,RMVar_hsa_circ_360593,RMVar_hsa_circ_75323,RMVar_hsa_circ_28290,RMVar_hsa_circ_343990 5543 RMVar_ID_5543 Human_SNP_ID_706949684 A-to-I Human chr22 - 49815395 49815395 49815395 GGAATTACAGGTGCACGTCACCACGCCCAACTAATTTTTGTGTTTTTAGTGGAGATGGGGTTTCG GGAATTACAGGTGCACGTCACCACGCCCAACTGATTTTTGTGTTTTTAGTGGAGATGGGGTTTCG T C BRD1 Ensembl:ENSG00000100425 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1308784827 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265202,RMVar_hsa_circ_360593,RMVar_hsa_circ_75323,RMVar_hsa_circ_28290,RMVar_hsa_circ_343990 5544 RMVar_ID_5544 Human_SNP_ID_706949685 A-to-I Human chr22 - 49815398 49815398 49815398 GCCGGAATTACAGGTGCACGTCACCACGCCCAACTAATTTTTGTGTTTTTAGTGGAGATGGGGTT GCCGGAATTACAGGTGCACGTCACCACGCCCAGCTAATTTTTGTGTTTTTAGTGGAGATGGGGTT T C BRD1 Ensembl:ENSG00000100425 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs777414481 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265202,RMVar_hsa_circ_360593,RMVar_hsa_circ_75323,RMVar_hsa_circ_28290,RMVar_hsa_circ_343990 5545 RMVar_ID_5545 Human_SNP_ID_706950036 A-to-I Human chr22 - 49816727 49816727 49816727 GGCCACCTGGCCCTAGTCTATTTTATAGAGACAGGGTCTCACTATGTTGTCCAGGCTGATCTTGA GGCCACCTGGCCCTAGTCTATTTTATAGAGACGGGGTCTCACTATGTTGTCCAGGCTGATCTTGA T C BRD1 Ensembl:ENSG00000100425 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1275636949 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265202,RMVar_hsa_circ_360593,RMVar_hsa_circ_75323,RMVar_hsa_circ_28290,RMVar_hsa_circ_343990 5546 RMVar_ID_5546 Human_SNP_ID_706950378 A-to-I Human chr22 - 49817955 49817955 49817955 CTGTTAGAAAAGTTGACTGGGTGCGGTGGCTCAGGCTAGTAATCCTAACACTGGAAGGCTGAGGT CTGTTAGAAAAGTTGACTGGGTGCGGTGGCTCGGGCTAGTAATCCTAACACTGGAAGGCTGAGGT T C BRD1 Ensembl:ENSG00000100425 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs551793823 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14527848,Human_RBP_ID_17148803,Human_RBP_ID_18791976 RMVar_hsa_circ_265202,RMVar_hsa_circ_360593,RMVar_hsa_circ_75323,RMVar_hsa_circ_28290,RMVar_hsa_circ_343990 5547 RMVar_ID_5547 Human_SNP_ID_706950874 A-to-I Human chr22 - 49819624 49819624 49819624 TAACATGGTGAAAACCCATCTGTACTAAAAATATAAAAATTAGCCAGGCGTGGTGGTGCGCGCCT TAACATGGTGAAAACCCATCTGTACTAAAAATGTAAAAATTAGCCAGGCGTGGTGGTGCGCGCCT T C BRD1 Ensembl:ENSG00000100425 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1017497002 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265202,RMVar_hsa_circ_360593,RMVar_hsa_circ_75323,RMVar_hsa_circ_28290,RMVar_hsa_circ_343990 5548 RMVar_ID_5548 Human_SNP_ID_706950958 A-to-I Human chr22 - 49819886 49819886 49819886 ACCTCAGGTGATCCACCCGCCTCGAACTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCGC ACCTCAGGTGATCCACCCGCCTCGAACTCCCACAGTGCTGGGATTACAGGCGTGAGCCACTGCGC T G BRD1 Ensembl:ENSG00000100425 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934343474 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25679216 RMVar_hsa_circ_265202,RMVar_hsa_circ_360593,RMVar_hsa_circ_75323,RMVar_hsa_circ_28290,RMVar_hsa_circ_343990 5549 RMVar_ID_5549 Human_SNP_ID_706951170 A-to-I Human chr22 - 49820538 49820538 49820538 GCAGTGGCGTGATCATGGCTTACAGTAGCCTCAAACTCTTGGACTCAAGCGATCTTCCCGCCTCA GCAGTGGCGTGATCATGGCTTACAGTAGCCTCTAACTCTTGGACTCAAGCGATCTTCCCGCCTCA T A BRD1 Ensembl:ENSG00000100425 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1009061890 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8553302,Human_RBP_ID_14527953 RMVar_hsa_circ_265202,RMVar_hsa_circ_360593,RMVar_hsa_circ_75323,RMVar_hsa_circ_28290,RMVar_hsa_circ_343990 5550 RMVar_ID_5550 Human_SNP_ID_706983521 A-to-I Human chr22 + 49925522 49925522 49925522 CTACGTCTGTGTGTGTCCTGACGGCTTCGAAGAAACGGAAGATGCCTGTGTGCCGCCGGCAGAGG CTACGTCTGTGTGTGTCCTGACGGCTTCGAAGGAACGGAAGATGCCTGTGTGCCGCCGGCAGAGG A G CRELD2 Ensembl:ENSG00000184164 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs11545763 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_583196,Human_RBP_ID_3962511,Human_RBP_ID_17660671,Human_RBP_ID_22454777,Human_RBP_ID_23954033,Human_RBP_ID_26346152 Human_Splice_Rec_2178193,Human_Splice_Rec_2178211,Human_Splice_Rec_2178243,Human_Splice_Rec_2178259,Human_Splice_Rec_2178291 Clinvar_Rec_38 GWAS_ID_227,GWAS_ID_228,GWAS_ID_229,GWAS_ID_230,GWAS_ID_231,GWAS_ID_232,GWAS_ID_233,GWAS_ID_234,GWAS_ID_235,GWAS_ID_236,GWAS_ID_237,GWAS_ID_238,GWAS_ID_239,GWAS_ID_240,GWAS_ID_241,GWAS_ID_242,GWAS_ID_243,GWAS_ID_244,GWAS_ID_245,GWAS_ID_246,GWAS_ID_247,GWAS_ID_248,GWAS_ID_249,GWAS_ID_250,GWAS_ID_251,GWAS_ID_252,GWAS_ID_253,GWAS_ID_254,GWAS_ID_255,GWAS_ID_256,GWAS_ID_257,GWAS_ID_258,GWAS_ID_259,GWAS_ID_260 5551 RMVar_ID_5551 Human_SNP_ID_706997205 A-to-I Human chr22 + 49963797 49963797 49963797 TCCCGGCCCCGCCTGTCAGAAGATGAACATGTATAGTGGCTAACTTAAGGGGAGTGGGTGACCCT TCCCGGCCCCGCCTGTCAGAAGATGAACATGTTTAGTGGCTAACTTAAGGGGAGTGGGTGACCCT A T PIM3 Ensembl:ENSG00000198355 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs906872743 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1613888,Human_RBP_ID_4706230,Human_RBP_ID_14528695,Human_RBP_ID_17988791,Human_RBP_ID_18330349,Human_RBP_ID_18792058,Human_RBP_ID_22821318,Human_RBP_ID_23954051,Human_RBP_ID_26500497 RMVar_hsa_circ_111261,RMVar_hsa_circ_87503,RMVar_hsa_circ_89523,RMVar_hsa_circ_215199,RMVar_hsa_circ_215200,RMVar_hsa_circ_215201 5552 RMVar_ID_5552 Human_SNP_ID_707072264 A-to-I Human chr22 + 50207249 50207249 50207249 GGTTCAAGCGATTCTCCTACCTCAGTCCCCCCAAATAGCTGGGGTTACAGACGTGCGCCACCACG GGTTCAAGCGATTCTCCTACCTCAGTCCCCCCGAATAGCTGGGGTTACAGACGTGCGCCACCACG A G SELENOO Ensembl:ENSG00000073169 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs574624434 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_332091,RMVar_hsa_circ_215217 5553 RMVar_ID_5553 Human_SNP_ID_707072276 A-to-I Human chr22 + 50207289 50207289 50207289 GGGGTTACAGACGTGCGCCACCACGTCCAGCTAATTTTTATATTTTTAGTACAGACAGGGTTTCT GGGGTTACAGACGTGCGCCACCACGTCCAGCTGATTTTTATATTTTTAGTACAGACAGGGTTTCT A G SELENOO Ensembl:ENSG00000073169 Protein coding intron GSE107867 ASD brains,cerebellum;ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs925659331 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_332091,RMVar_hsa_circ_215217 5554 RMVar_ID_5554 Human_SNP_ID_707072593 A-to-I Human chr22 + 50208345 50208345 50208345 CCAGCTACTCGGGAGGCTGAGGCAGTAGAATCACTTGAACCCAGAAGTTGGAGGTTGTGGTGAGG CCAGCTACTCGGGAGGCTGAGGCAGTAGAATCCCTTGAACCCAGAAGTTGGAGGTTGTGGTGAGG A C SELENOO Ensembl:ENSG00000073169 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs958376903 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_332091,RMVar_hsa_circ_215217 5555 RMVar_ID_5555 Human_SNP_ID_707074569 A-to-I Human chr22 + 50213480 50213462 50213481 TTATCTTGGAGAACTTTCTGTGTGCCCTGGAGAAGACGGTGTGCTCTCTTTTGCTGGGCAGAGCG TTATCTTGGAGAACT___________________GACGGTGTGCTCTCTTTTGCTGGGCAGAGCG TTTCTGTGTGCCCTGGAGAA T SELENOO Ensembl:ENSG00000073169 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1173757128 Functional Loss DEL dbSNP153 16..34 33 - - - Human_RBP_ID_14529161,Human_RBP_ID_17147217 RMVar_hsa_circ_12707,RMVar_hsa_circ_8288,RMVar_hsa_circ_61724,RMVar_hsa_circ_58023,RMVar_hsa_circ_123246,RMVar_hsa_circ_215218 5556 RMVar_ID_5556 Human_SNP_ID_707127149 A-to-I Human chr22 + 50352943 50352943 50352943 AAGTTTAGCTGAATGTGGTGGTGCATGCCTATAGTCCCAGCTACTGGGGAGGCTGAGGTAGGAGG AAGTTTAGCTGAATGTGGTGGTGCATGCCTATGGTCCCAGCTACTGGGGAGGCTGAGGTAGGAGG A G PPP6R2 Ensembl:ENSG00000100239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs192787979 Functional Loss SNV dbSNP153 33..33 33 - - - 5557 RMVar_ID_5557 Human_SNP_ID_707127830 A-to-I Human chr22 + 50355009 50355009 50355009 GAGACTACAGGTGCCTGCCACCATGCCTGGCTAATTTTTTATTTTTTGTGGAGACAGGGCCTTGC GAGACTACAGGTGCCTGCCACCATGCCTGGCTCATTTTTTATTTTTTGTGGAGACAGGGCCTTGC A C PPP6R2 Ensembl:ENSG00000100239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs926001387 Functional Loss SNV dbSNP153 33..33 33 - - - 5558 RMVar_ID_5558 Human_SNP_ID_707127831 A-to-I Human chr22 + 50355009 50355009 50355009 GAGACTACAGGTGCCTGCCACCATGCCTGGCTAATTTTTTATTTTTTGTGGAGACAGGGCCTTGC GAGACTACAGGTGCCTGCCACCATGCCTGGCTGATTTTTTATTTTTTGTGGAGACAGGGCCTTGC A G PPP6R2 Ensembl:ENSG00000100239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs926001387 Functional Loss SNV dbSNP153 33..33 33 - - - 5559 RMVar_ID_5559 Human_SNP_ID_707128197 A-to-I Human chr22 + 50355757 50355757 50355757 GTTAGCCAGGATGGTCTCGATCTCCTTACCTCATGATCCGCCCGCCTCGGCCTCCCAAATTGCTG GTTAGCCAGGATGGTCTCGATCTCCTTACCTCGTGATCCGCCCGCCTCGGCCTCCCAAATTGCTG A G PPP6R2 Ensembl:ENSG00000100239 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1192565872 Functional Loss SNV dbSNP153 33..33 33 - - - 5560 RMVar_ID_5560 Human_SNP_ID_707133925 A-to-I Human chr22 + 50374803 50374803 50374803 GGGCGTGGTGGTGCGCGCCTGTATTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAA GGGCGTGGTGGTGCGCGCCTGTATTCCCAGCTGCTCAGGAGGCTGAGGCAGGAGAATTGCTTGAA A G PPP6R2 Ensembl:ENSG00000100239 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs563526801 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3218,RMVar_hsa_circ_102802,RMVar_hsa_circ_271808,RMVar_hsa_circ_299255,RMVar_hsa_circ_370504,RMVar_hsa_circ_271960,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_215290,RMVar_hsa_circ_215292,RMVar_hsa_circ_215291,RMVar_hsa_circ_215289,RMVar_hsa_circ_215287,RMVar_hsa_circ_215284,RMVar_hsa_circ_215285 5561 RMVar_ID_5561 Human_SNP_ID_707134460 A-to-I Human chr22 + 50376562 50376562 50376562 CTTCTGTCTCAGCCTTCTGAGTGGCTGGGACTACAGGCACACACCACCACACCTGGCTAATTCTT CTTCTGTCTCAGCCTTCTGAGTGGCTGGGACTGCAGGCACACACCACCACACCTGGCTAATTCTT A G PPP6R2 Ensembl:ENSG00000100239 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs567105037 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3218,RMVar_hsa_circ_102802,RMVar_hsa_circ_271808,RMVar_hsa_circ_299255,RMVar_hsa_circ_370504,RMVar_hsa_circ_271960,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_215290,RMVar_hsa_circ_215292,RMVar_hsa_circ_215291,RMVar_hsa_circ_215289,RMVar_hsa_circ_215287,RMVar_hsa_circ_215284,RMVar_hsa_circ_215285 5562 RMVar_ID_5562 Human_SNP_ID_707134461 A-to-I Human chr22 + 50376562 50376562 50376562 CTTCTGTCTCAGCCTTCTGAGTGGCTGGGACTACAGGCACACACCACCACACCTGGCTAATTCTT CTTCTGTCTCAGCCTTCTGAGTGGCTGGGACTTCAGGCACACACCACCACACCTGGCTAATTCTT A T PPP6R2 Ensembl:ENSG00000100239 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs567105037 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3218,RMVar_hsa_circ_102802,RMVar_hsa_circ_271808,RMVar_hsa_circ_299255,RMVar_hsa_circ_370504,RMVar_hsa_circ_271960,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_215290,RMVar_hsa_circ_215292,RMVar_hsa_circ_215291,RMVar_hsa_circ_215289,RMVar_hsa_circ_215287,RMVar_hsa_circ_215284,RMVar_hsa_circ_215285 5563 RMVar_ID_5563 Human_SNP_ID_707136273 A-to-I Human chr22 + 50382931 50382931 50382931 ACAGTCTCAGCTCACTGCAACCTCTGCCTCCCAGACTCAAGCGATTCTCCTGCCTCAGTCTCCCG ACAGTCTCAGCTCACTGCAACCTCTGCCTCCCTGACTCAAGCGATTCTCCTGCCTCAGTCTCCCG A T PPP6R2 Ensembl:ENSG00000100239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs945264722 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3218,RMVar_hsa_circ_102802,RMVar_hsa_circ_271808,RMVar_hsa_circ_299255,RMVar_hsa_circ_370504,RMVar_hsa_circ_271960,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_215290,RMVar_hsa_circ_215292,RMVar_hsa_circ_215291,RMVar_hsa_circ_215289,RMVar_hsa_circ_215287,RMVar_hsa_circ_215284,RMVar_hsa_circ_215285 5564 RMVar_ID_5564 Human_SNP_ID_707136308 A-to-I Human chr22 + 50383099 50383099 50383099 ACCTCATGTGATCTGTCTGCCTTGGCCTCCCAAAGTTCTGGGATTACAGGCATAAGCCAGCACAC ACCTCATGTGATCTGTCTGCCTTGGCCTCCCAGAGTTCTGGGATTACAGGCATAAGCCAGCACAC A G PPP6R2 Ensembl:ENSG00000100239 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1022833006 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3218,RMVar_hsa_circ_102802,RMVar_hsa_circ_271808,RMVar_hsa_circ_299255,RMVar_hsa_circ_370504,RMVar_hsa_circ_271960,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_215290,RMVar_hsa_circ_215292,RMVar_hsa_circ_215291,RMVar_hsa_circ_215289,RMVar_hsa_circ_215287,RMVar_hsa_circ_215284,RMVar_hsa_circ_215285 5565 RMVar_ID_5565 Human_SNP_ID_707136796 A-to-I Human chr22 + 50384820 50384814 50384821 GGAAGTGCAGGGGCACAATCATGGCTCACTGCAGCTTCAACCTCCTGGGCTCAAGCGATCCTCCC GGAAGTGCAGGGGCACAATCATGGCTC_______CTTCAACCTCCTGGGCTCAAGCGATCCTCCC CACTGCAG C PPP6R2 Ensembl:ENSG00000100239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1169189673 Functional Loss DEL dbSNP153 28..34 33 - - - RMVar_hsa_circ_3218,RMVar_hsa_circ_102802,RMVar_hsa_circ_271808,RMVar_hsa_circ_299255,RMVar_hsa_circ_370504,RMVar_hsa_circ_271960,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_215290,RMVar_hsa_circ_215292,RMVar_hsa_circ_215291,RMVar_hsa_circ_215289,RMVar_hsa_circ_215287,RMVar_hsa_circ_215284,RMVar_hsa_circ_215285 5566 RMVar_ID_5566 Human_SNP_ID_707137764 A-to-I Human chr22 + 50388357 50388357 50388357 TTGAGGCTGCAGTGTGCCAAAATCCCACCACTACACTCCAGCCTTGGCAACAGAGCAAGACCCTA TTGAGGCTGCAGTGTGCCAAAATCCCACCACTTCACTCCAGCCTTGGCAACAGAGCAAGACCCTA A T PPP6R2 Ensembl:ENSG00000100239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs971930352 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3218,RMVar_hsa_circ_102802,RMVar_hsa_circ_271808,RMVar_hsa_circ_299255,RMVar_hsa_circ_370504,RMVar_hsa_circ_271960,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_215290,RMVar_hsa_circ_215292,RMVar_hsa_circ_215291,RMVar_hsa_circ_215289,RMVar_hsa_circ_215287,RMVar_hsa_circ_215284,RMVar_hsa_circ_215285 5567 RMVar_ID_5567 Human_SNP_ID_707138164 A-to-I Human chr22 + 50389764 50389764 50389764 GGGATTTCAGATGTGCACCACCATGCCTGGCTAATTTTTGTATTTGTGGTAGAGATGGGGTTGGC GGGATTTCAGATGTGCACCACCATGCCTGGCTGATTTTTGTATTTGTGGTAGAGATGGGGTTGGC A G PPP6R2 Ensembl:ENSG00000100239 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1283455086 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3218,RMVar_hsa_circ_102802,RMVar_hsa_circ_299255,RMVar_hsa_circ_370504,RMVar_hsa_circ_271960,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_215290,RMVar_hsa_circ_215291,RMVar_hsa_circ_215289,RMVar_hsa_circ_215287,RMVar_hsa_circ_215284,RMVar_hsa_circ_215285,RMVar_hsa_circ_69050,RMVar_hsa_circ_350104 5568 RMVar_ID_5568 Human_SNP_ID_707138265 A-to-I Human chr22 + 50390091 50390091 50390091 TCGGCTTACTACAACCTCTGCTTCTCGGGTTCAGGCGATTCTCCTGCCTCAGCCTCCCAAGTAGC TCGGCTTACTACAACCTCTGCTTCTCGGGTTCGGGCGATTCTCCTGCCTCAGCCTCCCAAGTAGC A G PPP6R2 Ensembl:ENSG00000100239 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1311462805 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3218,RMVar_hsa_circ_102802,RMVar_hsa_circ_299255,RMVar_hsa_circ_370504,RMVar_hsa_circ_271960,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_215290,RMVar_hsa_circ_215291,RMVar_hsa_circ_215289,RMVar_hsa_circ_215287,RMVar_hsa_circ_215284,RMVar_hsa_circ_215285,RMVar_hsa_circ_69050,RMVar_hsa_circ_350104 5569 RMVar_ID_5569 Human_SNP_ID_707138383 A-to-I Human chr22 + 50390538 50390538 50390538 GTAACAGGCCAGGCGTGGTGGTTCACACCTGTATTCCCAGCATTTTGGGAGGCTGAGGCAGGAGA GTAACAGGCCAGGCGTGGTGGTTCACACCTGTGTTCCCAGCATTTTGGGAGGCTGAGGCAGGAGA A G PPP6R2 Ensembl:ENSG00000100239 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1379602792 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3218,RMVar_hsa_circ_102802,RMVar_hsa_circ_299255,RMVar_hsa_circ_370504,RMVar_hsa_circ_271960,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_215290,RMVar_hsa_circ_215291,RMVar_hsa_circ_215289,RMVar_hsa_circ_215287,RMVar_hsa_circ_215284,RMVar_hsa_circ_215285,RMVar_hsa_circ_69050,RMVar_hsa_circ_350104 5570 RMVar_ID_5570 Human_SNP_ID_707139925 A-to-I Human chr22 + 50395810 50395810 50395810 GCTGGTTTCAGACTCCTGGGCTCAAGCAATCCACCCACCTCGGCCTCCCAAAGTGCTGGGATTAT GCTGGTTTCAGACTCCTGGGCTCAAGCAATCCTCCCACCTCGGCCTCCCAAAGTGCTGGGATTAT A T PPP6R2 Ensembl:ENSG00000100239 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs551799228 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17572893 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 5571 RMVar_ID_5571 Human_SNP_ID_707141661 A-to-I Human chr22 + 50401346 50401346 50401346 CTCCTGCCTCAGCCTCCCGTGTAGCTGGAACTACAGACGCCCACCACCACGCCCGGCTAATTTTT CTCCTGCCTCAGCCTCCCGTGTAGCTGGAACTGCAGACGCCCACCACCACGCCCGGCTAATTTTT A G PPP6R2 Ensembl:ENSG00000100239 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900733619 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14530637 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 5572 RMVar_ID_5572 Human_SNP_ID_707142153 A-to-I Human chr22 + 50403060 50403060 50403060 CATGGTAAAACCCCGTCTCTACCAAAAATACAAAAGTTAGCCGAGCATGGTGGTGCATGCCTGTA CATGGTAAAACCCCGTCTCTACCAAAAATACAGAAGTTAGCCGAGCATGGTGGTGCATGCCTGTA A G PPP6R2 Ensembl:ENSG00000100239 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1272288843 Functional Loss SNV dbSNP153 33..33 33 - - - 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 5573 RMVar_ID_5573 Human_SNP_ID_707142154 A-to-I Human chr22 + 50403060 50403060 50403060 CATGGTAAAACCCCGTCTCTACCAAAAATACAAAAGTTAGCCGAGCATGGTGGTGCATGCCTGTA CATGGTAAAACCCCGTCTCTACCAAAAATACATAAGTTAGCCGAGCATGGTGGTGCATGCCTGTA A T PPP6R2 Ensembl:ENSG00000100239 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1272288843 Functional Loss SNV dbSNP153 33..33 33 - - - 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 5574 RMVar_ID_5574 Human_SNP_ID_707143553 A-to-I Human chr22 + 50408023 50408023 50408023 CTCCCACCTCGGCCTCCTGAGTAGCTGGGACTACAGGCACATAACACCACACCTGGCTAGTTTTT CTCCCACCTCGGCCTCCTGAGTAGCTGGGACTTCAGGCACATAACACCACACCTGGCTAGTTTTT A T PPP6R2 Ensembl:ENSG00000100239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1569436868 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4858,RMVar_hsa_circ_3218,RMVar_hsa_circ_102802,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_215287,RMVar_hsa_circ_215284,RMVar_hsa_circ_215285,RMVar_hsa_circ_215296,RMVar_hsa_circ_336539,RMVar_hsa_circ_353939,RMVar_hsa_circ_115339,RMVar_hsa_circ_119587,RMVar_hsa_circ_15996,RMVar_hsa_circ_215297,RMVar_hsa_circ_215298,RMVar_hsa_circ_323326,RMVar_hsa_circ_334170,RMVar_hsa_circ_308440,RMVar_hsa_circ_12727,RMVar_hsa_circ_45138,RMVar_hsa_circ_73474,RMVar_hsa_circ_215299,RMVar_hsa_circ_215300,RMVar_hsa_circ_353536,RMVar_hsa_circ_215301 5575 RMVar_ID_5575 Human_SNP_ID_707144212 A-to-I Human chr22 + 50410623 50410623 50410623 ATTCTCGTGCCTCAGCCTCCCGTCTGGGGGATAGAGTGAGATTCTGTCTCCAAAAAAAAGAAAAA ATTCTCGTGCCTCAGCCTCCCGTCTGGGGGATGGAGTGAGATTCTGTCTCCAAAAAAAAGAAAAA A G PPP6R2 Ensembl:ENSG00000100239 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1403187847 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7092693,Human_RBP_ID_22725534 RMVar_hsa_circ_4858,RMVar_hsa_circ_3218,RMVar_hsa_circ_102802,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_215287,RMVar_hsa_circ_215284,RMVar_hsa_circ_215285,RMVar_hsa_circ_215296,RMVar_hsa_circ_336539,RMVar_hsa_circ_353939,RMVar_hsa_circ_115339,RMVar_hsa_circ_119587,RMVar_hsa_circ_15996,RMVar_hsa_circ_215297,RMVar_hsa_circ_215298,RMVar_hsa_circ_323326,RMVar_hsa_circ_334170,RMVar_hsa_circ_308440,RMVar_hsa_circ_12727,RMVar_hsa_circ_45138,RMVar_hsa_circ_73474,RMVar_hsa_circ_215299,RMVar_hsa_circ_215300,RMVar_hsa_circ_353536,RMVar_hsa_circ_215301 5576 RMVar_ID_5576 Human_SNP_ID_707144400 A-to-I Human chr22 + 50411381 50411381 50411381 TGGGGCTGAGACAGGAGAATCACTTGAACCTGAAGGCGGAGGTTGCAGTGAGCCAAGATTGGGCC TGGGGCTGAGACAGGAGAATCACTTGAACCTGCAGGCGGAGGTTGCAGTGAGCCAAGATTGGGCC A C PPP6R2 Ensembl:ENSG00000100239 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1393517334 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17573112,Human_RBP_ID_22480256,Human_RBP_ID_22725535 RMVar_hsa_circ_4858,RMVar_hsa_circ_3218,RMVar_hsa_circ_102802,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_215287,RMVar_hsa_circ_215284,RMVar_hsa_circ_215285,RMVar_hsa_circ_215296,RMVar_hsa_circ_336539,RMVar_hsa_circ_353939,RMVar_hsa_circ_115339,RMVar_hsa_circ_119587,RMVar_hsa_circ_15996,RMVar_hsa_circ_215297,RMVar_hsa_circ_215298,RMVar_hsa_circ_323326,RMVar_hsa_circ_334170,RMVar_hsa_circ_308440,RMVar_hsa_circ_12727,RMVar_hsa_circ_45138,RMVar_hsa_circ_73474,RMVar_hsa_circ_215299,RMVar_hsa_circ_215300,RMVar_hsa_circ_353536,RMVar_hsa_circ_215301 5577 RMVar_ID_5577 Human_SNP_ID_707144650 A-to-I Human chr22 + 50412228 50412228 50412228 TTTTTCTTTTTTTGGAGATAGACTCTCACTCTATCCCCCAGGCTGGAGTGCAGTGGTGTGATCTC TTTTTCTTTTTTTGGAGATAGACTCTCACTCTGTCCCCCAGGCTGGAGTGCAGTGGTGTGATCTC A G PPP6R2 Ensembl:ENSG00000100239 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1230757163 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17572896 RMVar_hsa_circ_4858,RMVar_hsa_circ_3218,RMVar_hsa_circ_102802,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_215287,RMVar_hsa_circ_215284,RMVar_hsa_circ_215285,RMVar_hsa_circ_215296,RMVar_hsa_circ_336539,RMVar_hsa_circ_353939,RMVar_hsa_circ_115339,RMVar_hsa_circ_119587,RMVar_hsa_circ_15996,RMVar_hsa_circ_215297,RMVar_hsa_circ_215298,RMVar_hsa_circ_323326,RMVar_hsa_circ_334170,RMVar_hsa_circ_308440,RMVar_hsa_circ_12727,RMVar_hsa_circ_45138,RMVar_hsa_circ_73474,RMVar_hsa_circ_215299,RMVar_hsa_circ_215300,RMVar_hsa_circ_353536,RMVar_hsa_circ_215301 5578 RMVar_ID_5578 Human_SNP_ID_707144962 A-to-I Human chr22 + 50413197 50413197 50413197 GGCTGGTCTCGACCTCAGTCTGGTCTGACCTCAGGTGATCCACCCACCTCGGCCTCCCAAAGTGC GGCTGGTCTCGACCTCAGTCTGGTCTGACCTCTGGTGATCCACCCACCTCGGCCTCCCAAAGTGC A T PPP6R2 Ensembl:ENSG00000100239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1433488365 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4858,RMVar_hsa_circ_3218,RMVar_hsa_circ_102802,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_215287,RMVar_hsa_circ_215284,RMVar_hsa_circ_215285,RMVar_hsa_circ_215296,RMVar_hsa_circ_336539,RMVar_hsa_circ_353939,RMVar_hsa_circ_115339,RMVar_hsa_circ_119587,RMVar_hsa_circ_15996,RMVar_hsa_circ_215297,RMVar_hsa_circ_215298,RMVar_hsa_circ_323326,RMVar_hsa_circ_334170,RMVar_hsa_circ_308440,RMVar_hsa_circ_12727,RMVar_hsa_circ_45138,RMVar_hsa_circ_73474,RMVar_hsa_circ_215299,RMVar_hsa_circ_215300,RMVar_hsa_circ_353536,RMVar_hsa_circ_215301 5579 RMVar_ID_5579 Human_SNP_ID_707148937 A-to-I Human chr22 + 50427068 50427068 50427068 AAAATTAGCTGGGTGTGGTGGCATGTGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA AAAATTAGCTGGGTGTGGTGGCATGTGCCTGTGGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA A G PPP6R2 Ensembl:ENSG00000100239 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1056622258 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_12727,RMVar_hsa_circ_45138,RMVar_hsa_circ_23987,RMVar_hsa_circ_79344,RMVar_hsa_circ_215303,RMVar_hsa_circ_128190,RMVar_hsa_circ_215305 5580 RMVar_ID_5580 Human_SNP_ID_707153931 A-to-I Human chr22 + 50442728 50442728 50442728 TCCGCCACCACCAGGCCCGGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACTGTGTTAG TCCGCCACCACCAGGCCCGGCTAATTTTTTGTGTTTTTAGTAGAGACGGGGTTTCACTGTGTTAG A G PPP6R2 Ensembl:ENSG00000100239 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935259927 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119587,RMVar_hsa_circ_215297 5581 RMVar_ID_5581 Human_SNP_ID_707154005 A-to-I Human chr22 + 50442891 50442891 50442891 TGAAATTCTTAACAGTCTTTACCCTGCCAGGCACAGTGGCTCACGCCTGTAATCCCAGCACTTTG TGAAATTCTTAACAGTCTTTACCCTGCCAGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTTTG A G PPP6R2 Ensembl:ENSG00000100239 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048335977 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119587,RMVar_hsa_circ_215297 5582 RMVar_ID_5582 Human_SNP_ID_707154007 A-to-I Human chr22 + 50442893 50442893 50442893 AAATTCTTAACAGTCTTTACCCTGCCAGGCACAGTGGCTCACGCCTGTAATCCCAGCACTTTGGG AAATTCTTAACAGTCTTTACCCTGCCAGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG A G PPP6R2 Ensembl:ENSG00000100239 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs368775187 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119587,RMVar_hsa_circ_215297 5583 RMVar_ID_5583 Human_SNP_ID_707154015 A-to-I Human chr22 + 50442909 50442909 50442909 TTACCCTGCCAGGCACAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGTGG TTACCCTGCCAGGCACAGTGGCTCACGCCTGTCATCCCAGCACTTTGGGAGGCCGAGGTGGGTGG A C PPP6R2 Ensembl:ENSG00000100239 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1246045411 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119587,RMVar_hsa_circ_215297 5584 RMVar_ID_5584 Human_SNP_ID_707154078 A-to-I Human chr22 + 50443054 50443054 50443054 AGGCGTGGTGGCAGGCGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAA AGGCGTGGTGGCAGGCGCCTGTAGTCCCAGCTGCTTGGGAGGCTGAGGCAGGAGAATCGCTTGAA A G PPP6R2 Ensembl:ENSG00000100239 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs895384696 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_152025 RMVar_hsa_circ_119587,RMVar_hsa_circ_215297 5585 RMVar_ID_5585 Human_SNP_ID_707154880 A-to-I Human chr22 + 50444665 50444665 50444665 TTGTTTTGTTTTTAAAGAATACAGAAGGAGCCAAGCTTTTTTGCACTTTGTATCCAGCTGCAAGC TTGTTTTGTTTTTAAAGAATACAGAAGGAGCCGAGCTTTTTTGCACTTTGTATCCAGCTGCAAGC A G PPP6R2 Ensembl:ENSG00000100239 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs531307427 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5119832,Human_RBP_ID_14531263,Human_RBP_ID_18168892 5586 RMVar_ID_5586 Human_SNP_ID_707178721 A-to-I Human chr22 - 50503492 50503492 50503492 CCCCGCTGGCACCAGTCAGCGGGGAGAAGCGCAGGCCAGCCTCCCAGAAAGACTCCGGAGCTGCC CCCCGCTGGCACCAGTCAGCGGGGAGAAGCGCGGGCCAGCCTCCCAGAAAGACTCCGGAGCTGCC T C LMF2 Ensembl:ENSG00000100258 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs759486806 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10864,Human_RBP_ID_22768360 RMVar_hsa_circ_98001,RMVar_hsa_circ_108211,RMVar_hsa_circ_113377,RMVar_hsa_circ_115325,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_215349,RMVar_hsa_circ_215346,RMVar_hsa_circ_215344,RMVar_hsa_circ_215341,RMVar_hsa_circ_215342 5587 RMVar_ID_5587 Human_SNP_ID_707205707 A-to-I Human chr22 - 50579738 50579738 50579738 GAGCAGAGAAAACTGGAAGAAGATTTGCTGGTAGAAGTCAGTCGGTGAGGAAGGAGGGGCAGGGT GAGCAGAGAAAACTGGAAGAAGATTTGCTGGTGGAAGTCAGTCGGTGAGGAAGGAGGGGCAGGGT T C CHKB-CPT1B,CHKB Ensembl:ENSG00000254413,Ensembl:ENSG00000100288 Protein coding,Protein coding exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1413085946 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5601759,Human_RBP_ID_14531922,Human_RBP_ID_23015186 Human_Splice_Rec_2181550,Human_Splice_Rec_2181551,Human_Splice_Rec_2181593,Human_Splice_Rec_2181638,Human_Splice_Rec_2181658,Human_Splice_Rec_2181659,Human_Splice_Rec_2181666,Human_Splice_Rec_2181667,Human_Splice_Rec_2181678,Human_Splice_Rec_2181679,Human_Splice_Rec_2181692,Human_Splice_Rec_2181693,Human_Splice_Rec_2181710,Human_Splice_Rec_2181711,Human_Splice_Rec_2181730,Human_Splice_Rec_2181731,Human_Splice_Rec_2181744,Human_Splice_Rec_2181745,Human_Splice_Rec_2181760,Human_Splice_Rec_2181761 5588 RMVar_ID_5588 Human_SNP_ID_707219473 A-to-I Human chr22 - 50623555 50623555 50623555 GGTAGCATTTGTCCTAGCAATTTGGGAGGTTGAGGTGGGAGAATCACTTCAGCCCACTAGGTCGA GGTAGCATTTGTCCTAGCAATTTGGGAGGTTGGGGTGGGAGAATCACTTCAGCCCACTAGGTCGA T C ARSA Ensembl:ENSG00000100299 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005504967 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94609,RMVar_hsa_circ_215370 5589 RMVar_ID_5589 Human_SNP_ID_707219534 A-to-I Human chr22 - 50623777 50623777 50623777 CTCCTGCCTCAGCCTCCCTAGTAGCTGGAACTACAGGTGTGTGCTGCCATGCCCAGCTAATTTTT CTCCTGCCTCAGCCTCCCTAGTAGCTGGAACTGCAGGTGTGTGCTGCCATGCCCAGCTAATTTTT T C ARSA Ensembl:ENSG00000100299 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs866107366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2181869 RMVar_hsa_circ_94609,RMVar_hsa_circ_215370 5590 RMVar_ID_5590 Human_SNP_ID_707219551 A-to-I Human chr22 - 50623855 50623855 50623855 TCGCTCTGTCGCCCAGGCTAGAGTGCAGTGGTACCATCTCCGCTCACTGCAACCTCCGCCTCCCG TCGCTCTGTCGCCCAGGCTAGAGTGCAGTGGTTCCATCTCCGCTCACTGCAACCTCCGCCTCCCG T A ARSA Ensembl:ENSG00000100299 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs957072421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2181868,Human_Splice_Rec_2181869 RMVar_hsa_circ_94609,RMVar_hsa_circ_215370 5591 RMVar_ID_5591 Human_SNP_ID_707219552 A-to-I Human chr22 - 50623855 50623855 50623855 TCGCTCTGTCGCCCAGGCTAGAGTGCAGTGGTACCATCTCCGCTCACTGCAACCTCCGCCTCCCG TCGCTCTGTCGCCCAGGCTAGAGTGCAGTGGTGCCATCTCCGCTCACTGCAACCTCCGCCTCCCG T C ARSA Ensembl:ENSG00000100299 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs957072421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2181868,Human_Splice_Rec_2181869 RMVar_hsa_circ_94609,RMVar_hsa_circ_215370 5592 RMVar_ID_5592 Human_SNP_ID_707219673 A-to-I Human chr22 - 50624106 50624105 50624107 GATCGCACCATTGCACTCCAGCCTGGGCAACAAGAGAAAAACTCTGTCTCAAAAAACAAAAAATC GATCGCACCATTGCACTCCAGCCTGGGCAAC__GAGAAAAACTCTGTCTCAAAAAACAAAAAATC CTT C ARSA Ensembl:ENSG00000100299 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1401333841 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_94609,RMVar_hsa_circ_215370 5593 RMVar_ID_5593 Human_SNP_ID_707219677 A-to-I Human chr22 - 50624132 50624132 50624132 GGGAGGCGGTGGTTGCAGTGAGCCGAGATCGCACCATTGCACTCCAGCCTGGGCAACAAGAGAAA GGGAGGCGGTGGTTGCAGTGAGCCGAGATCGCGCCATTGCACTCCAGCCTGGGCAACAAGAGAAA T C ARSA Ensembl:ENSG00000100299 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490832,GSM3490833,GSM3490834 Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 31158229,32596459 RNA-Seq:(High) rs1395424621 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94609,RMVar_hsa_circ_215370 5594 RMVar_ID_5594 Human_SNP_ID_707244729 A-to-I Human chr22 + 50708946 50708946 50708946 AGGAGTTTGAGACCAGCCTGGGGAACATGGCGAAACCCTATCTCTACTAAAAATACAAAAATTAT AGGAGTTTGAGACCAGCCTGGGGAACATGGCGGAACCCTATCTCTACTAAAAATACAAAAATTAT A G SHANK3 Ensembl:ENSG00000251322 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs890601264 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268566,RMVar_hsa_circ_378835,RMVar_hsa_circ_61556,RMVar_hsa_circ_350621 5595 RMVar_ID_5595 Human_SNP_ID_707244764 A-to-I Human chr22 + 50709084 50709084 50709084 ACGTGGAGGTTGCAGTGAGCCAAGATCATGCCAGTGCACTCCAGCCTGGGCAACAGAGCGAGACC ACGTGGAGGTTGCAGTGAGCCAAGATCATGCCTGTGCACTCCAGCCTGGGCAACAGAGCGAGACC A T SHANK3 Ensembl:ENSG00000251322 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1244367509 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268566,RMVar_hsa_circ_378835,RMVar_hsa_circ_61556,RMVar_hsa_circ_350621 5596 RMVar_ID_5596 Human_SNP_ID_505804917 A-to-I Human chr12 + 70254826 70254825 70254826 AACATGGAAAACCCTGTCTCTACTAAAAATACAAAAAATTAGCCAGGCATGGTGGCACGTGTCTC AACATGGAAAACCCTGTCTCTACTAAAAATAC_AAAAATTAGCCAGGCATGGTGGCACGTGTCTC CA C CNOT2 Ensembl:ENSG00000111596 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1362514996 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_124403,RMVar_hsa_circ_92345,RMVar_hsa_circ_158218,RMVar_hsa_circ_158220 5597 RMVar_ID_5597 Human_SNP_ID_505812145 A-to-I Human chr12 + 70284324 70284324 70284324 TGGAGTGCAGTGGCACCATCTCCGCTCACTGCAACCTCTGCCACCTGGGTTCAAGCAATTTTCGT TGGAGTGCAGTGGCACCATCTCCGCTCACTGCGACCTCTGCCACCTGGGTTCAAGCAATTTTCGT A G CNOT2 Ensembl:ENSG00000111596 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1255234627 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124403,RMVar_hsa_circ_92345,RMVar_hsa_circ_158218,RMVar_hsa_circ_158222,RMVar_hsa_circ_158226,RMVar_hsa_circ_304055,RMVar_hsa_circ_158220,RMVar_hsa_circ_352944,RMVar_hsa_circ_375722,RMVar_hsa_circ_307286,RMVar_hsa_circ_272837,RMVar_hsa_circ_277640,RMVar_hsa_circ_270807,RMVar_hsa_circ_158224,RMVar_hsa_circ_158225,RMVar_hsa_circ_158223,RMVar_hsa_circ_158227 5598 RMVar_ID_5598 Human_SNP_ID_505827605 A-to-I Human chr12 + 70347512 70347512 70347512 AAAATTAGCTGGGCCTGGTGGAGGGTGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTAGCTGGGCCTGGTGGAGGGTGCCTGTGGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA A G CNOT2 Ensembl:ENSG00000111596 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs995078570 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113264,RMVar_hsa_circ_158245,RMVar_hsa_circ_114078,RMVar_hsa_circ_158246 5599 RMVar_ID_5599 Human_SNP_ID_505887739 A-to-I Human chr12 - 70599910 70599910 70599910 GTAGCTATTCACAGGCACTATTATGATGCACTATAGCCTCCAATACCTGGACCCAAGCAACCCTC GTAGCTATTCACAGGCACTATTATGATGCACTGTAGCCTCCAATACCTGGACCCAAGCAACCCTC T C PTPRB Ensembl:ENSG00000127329 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1198588542 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37968,RMVar_hsa_circ_158256,RMVar_hsa_circ_91701,RMVar_hsa_circ_98964,RMVar_hsa_circ_266653,RMVar_hsa_circ_158258 5600 RMVar_ID_5600 Human_SNP_ID_506129612 A-to-I Human chr12 - 71615592 71615592 71615592 GAATCACTTGAACCTGGGAGGTGGAGGTTGCAATGAGCTGAGATCATGCCACTGCACTCCAGCCT GAATCACTTGAACCTGGGAGGTGGAGGTTGCAGTGAGCTGAGATCATGCCACTGCACTCCAGCCT T C ZFC3H1 Ensembl:ENSG00000133858 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs888803670 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_158266,RMVar_hsa_circ_158267,RMVar_hsa_circ_120461,RMVar_hsa_circ_50848,RMVar_hsa_circ_10921,RMVar_hsa_circ_37631,RMVar_hsa_circ_53141,RMVar_hsa_circ_265041,RMVar_hsa_circ_7401,RMVar_hsa_circ_69966,RMVar_hsa_circ_107487,RMVar_hsa_circ_72760,RMVar_hsa_circ_54137,RMVar_hsa_circ_158269 5601 RMVar_ID_5601 Human_SNP_ID_506129712 A-to-I Human chr12 - 71616098 71616098 71616098 GAGATCTTGGGGTTTCACCCAAGTTGTTAGCCAGGCTGATCTTGAACTCCTGACCTTAAGTGAAC GAGATCTTGGGGTTTCACCCAAGTTGTTAGCCGGGCTGATCTTGAACTCCTGACCTTAAGTGAAC T C ZFC3H1 Ensembl:ENSG00000133858 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,frontal_cortex - 29129909,30559470 RNA-Seq:(High) rs1480685135 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_158266,RMVar_hsa_circ_158267,RMVar_hsa_circ_120461,RMVar_hsa_circ_50848,RMVar_hsa_circ_10921,RMVar_hsa_circ_37631,RMVar_hsa_circ_53141,RMVar_hsa_circ_265041,RMVar_hsa_circ_7401,RMVar_hsa_circ_69966,RMVar_hsa_circ_107487,RMVar_hsa_circ_72760,RMVar_hsa_circ_54137,RMVar_hsa_circ_158269 5602 RMVar_ID_5602 Human_SNP_ID_506129747 A-to-I Human chr12 - 71616258 71616258 71616258 GGGTCTCACTTTATAACATGGGCTGGAGCACAATGGTGTGATCTCAGCTCACTGTAACCTCTGCC GGGTCTCACTTTATAACATGGGCTGGAGCACAGTGGTGTGATCTCAGCTCACTGTAACCTCTGCC T C ZFC3H1 Ensembl:ENSG00000133858 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs944558942 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_158266,RMVar_hsa_circ_158267,RMVar_hsa_circ_120461,RMVar_hsa_circ_50848,RMVar_hsa_circ_10921,RMVar_hsa_circ_37631,RMVar_hsa_circ_53141,RMVar_hsa_circ_265041,RMVar_hsa_circ_7401,RMVar_hsa_circ_69966,RMVar_hsa_circ_107487,RMVar_hsa_circ_72760,RMVar_hsa_circ_54137,RMVar_hsa_circ_158269 5603 RMVar_ID_5603 Human_SNP_ID_506140269 A-to-I Human chr12 - 71657841 71657841 71657841 GGGACTACAGGCCTGCACCACCACGCCTGGCTAATTTTTTAATTTTTAGTAGAGATGGGGTTTCA GGGACTACAGGCCTGCACCACCACGCCTGGCTGATTTTTTAATTTTTAGTAGAGATGGGGTTTCA T C ZFC3H1 Ensembl:ENSG00000133858 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs775951019 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_158266,RMVar_hsa_circ_158276,RMVar_hsa_circ_94801,RMVar_hsa_circ_158284,RMVar_hsa_circ_158287,RMVar_hsa_circ_158289,RMVar_hsa_circ_118996,RMVar_hsa_circ_158290,RMVar_hsa_circ_158292,RMVar_hsa_circ_158291 5604 RMVar_ID_5604 Human_SNP_ID_506140285 A-to-I Human chr12 - 71657902 71657902 71657902 TCCCTGCAACCTCCGCCTCCTGAGTTCAAGCAATTCTCTTGCCTCAGCGTCTCAAGTACCTGGGA TCCCTGCAACCTCCGCCTCCTGAGTTCAAGCAGTTCTCTTGCCTCAGCGTCTCAAGTACCTGGGA T C ZFC3H1 Ensembl:ENSG00000133858 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs12314790 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_158266,RMVar_hsa_circ_158276,RMVar_hsa_circ_94801,RMVar_hsa_circ_158284,RMVar_hsa_circ_158287,RMVar_hsa_circ_158289,RMVar_hsa_circ_118996,RMVar_hsa_circ_158290,RMVar_hsa_circ_158292,RMVar_hsa_circ_158291 5605 RMVar_ID_5605 Human_SNP_ID_506140436 A-to-I Human chr12 - 71658453 71658453 71658453 GAAACTCCATCTCTACTAAAAATACAAAAATTAGCTGGGCATGGTGGCACGCACCTGTAATCCAA GAAACTCCATCTCTACTAAAAATACAAAAATTCGCTGGGCATGGTGGCACGCACCTGTAATCCAA T G ZFC3H1 Ensembl:ENSG00000133858 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1310037297 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_158266,RMVar_hsa_circ_158276,RMVar_hsa_circ_94801,RMVar_hsa_circ_158284,RMVar_hsa_circ_158287,RMVar_hsa_circ_158289,RMVar_hsa_circ_118996,RMVar_hsa_circ_158290,RMVar_hsa_circ_158292,RMVar_hsa_circ_158291 5606 RMVar_ID_5606 Human_SNP_ID_506151080 A-to-I Human chr12 + 71702343 71702343 71702343 TGCTTTTTTTGTTTATGTGTTTGTTTTTTGAGACAGAGTCTCACACTGTGGCCCAGGCTGGACTC TGCTTTTTTTGTTTATGTGTTTGTTTTTTGAGGCAGAGTCTCACACTGTGGCCCAGGCTGGACTC A G TMEM19 Ensembl:ENSG00000139291 Protein coding 3'UTR GSE38233;GSE100210;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,cerebellum - 24183664,29129909,30559470 RNA-Seq:(High) rs936463357 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3414031,Human_RBP_ID_26419720 5607 RMVar_ID_5607 Human_SNP_ID_506151081 A-to-I Human chr12 + 71702345 71702345 71702345 CTTTTTTTGTTTATGTGTTTGTTTTTTGAGACAGAGTCTCACACTGTGGCCCAGGCTGGACTCCA CTTTTTTTGTTTATGTGTTTGTTTTTTGAGACGGAGTCTCACACTGTGGCCCAGGCTGGACTCCA A G TMEM19 Ensembl:ENSG00000139291 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs1055258573 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3414031,Human_RBP_ID_26419720 5608 RMVar_ID_5608 Human_SNP_ID_506151121 A-to-I Human chr12 + 71702505 71702505 71702505 GCCCGGCTAATTTTTGTATTTTCAGTAGAGACAGGGTTTCGCCACGTTGGCTAGGCTGGTCTCGA GCCCGGCTAATTTTTGTATTTTCAGTAGAGACGGGGTTTCGCCACGTTGGCTAGGCTGGTCTCGA A G TMEM19 Ensembl:ENSG00000139291 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs988400372 Functional Loss SNV dbSNP153 33..33 33 - - - 5609 RMVar_ID_5609 Human_SNP_ID_506151142 A-to-I Human chr12 + 71702587 71702587 71702587 ATCTGCCCATCTCAGCCTCCCAAAGATCTATTACAAGATGTGAGCCACTGTGCCCAGCCACCAGG ATCTGCCCATCTCAGCCTCCCAAAGATCTATTGCAAGATGTGAGCCACTGTGCCCAGCCACCAGG A G TMEM19 Ensembl:ENSG00000139291 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1235081380 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4241145 5610 RMVar_ID_5610 Human_SNP_ID_506151143 A-to-I Human chr12 + 71702589 71702589 71702589 CTGCCCATCTCAGCCTCCCAAAGATCTATTACAAGATGTGAGCCACTGTGCCCAGCCACCAGGGC CTGCCCATCTCAGCCTCCCAAAGATCTATTACGAGATGTGAGCCACTGTGCCCAGCCACCAGGGC A G TMEM19 Ensembl:ENSG00000139291 Protein coding 3'UTR GSE107867 ASD brains,cerebellum;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs886259492 Functional Loss SNV dbSNP153 33..33 33 - - - 5611 RMVar_ID_5611 Human_SNP_ID_506151237 A-to-I Human chr12 + 71702996 71702996 71702996 GAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACACCGTCTCTACTAAAAATACAAA GAGGTCAGGAGTTCGAGACCAGCCTGGCCAACGTGGTGAAACACCGTCTCTACTAAAAATACAAA A G TMEM19 Ensembl:ENSG00000139291 Protein coding 3'UTR GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1421229876 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_116234 5612 RMVar_ID_5612 Human_SNP_ID_506151244 A-to-I Human chr12 + 71703024 71703024 71703024 CAACATGGTGAAACACCGTCTCTACTAAAAATACAAAAAATTAGGTGTGGTGGTGCGTGCCTGTA CAACATGGTGAAACACCGTCTCTACTAAAAATGCAAAAAATTAGGTGTGGTGGTGCGTGCCTGTA A G TMEM19 Ensembl:ENSG00000139291 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1245935557 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26419722 5613 RMVar_ID_5613 Human_SNP_ID_506152057 A-to-I Human chr12 + 71706164 71706164 71706164 CGCCTCCTGGGTTCAAGTGATTCCCCTGCCTCAGCTTCCTGAGTAGCTGGGACTACAGGCGTGCA CGCCTCCTGGGTTCAAGTGATTCCCCTGCCTCCGCTTCCTGAGTAGCTGGGACTACAGGCGTGCA A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1206982760 Functional Loss SNV dbSNP153 33..33 33 - - - 5614 RMVar_ID_5614 Human_SNP_ID_506168800 A-to-I Human chr12 + 71774577 71774576 71774577 GGTCAGGAGTTCAAAACCAGCCTGGCCAACATAGTGAAACCCCGCTCTAATAAAAATACAAAAAT GGTCAGGAGTTCAAAACCAGCCTGGCCAACAT_GTGAAACCCCGCTCTAATAAAAATACAAAAAT TA T RAB21 Ensembl:ENSG00000080371 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1370124112 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_44485,RMVar_hsa_circ_309111 5615 RMVar_ID_5615 Human_SNP_ID_506173653 A-to-I Human chr12 + 71793965 71793965 71793965 TGGCTGGGAGCCATGGCTCATGCCTGTAATCCAGCACTTTGGGAGGCTGAGGTGGGTGGATGGAT TGGCTGGGAGCCATGGCTCATGCCTGTAATCCGGCACTTTGGGAGGCTGAGGTGGGTGGATGGAT A G RAB21 Ensembl:ENSG00000080371 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs538267397 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2353209 5616 RMVar_ID_5616 Human_SNP_ID_506173718 A-to-I Human chr12 + 71794226 71794221 71794227 CCTGGACGACAGAGTGAGGCCCTGTCTCAAAAAAAGAAAAAAGAAAAAAAAAAGTTAAAAGTTGT CCTGGACGACAGAGTGAGGCCCTGTCTC______AGAAAAAAGAAAAAAAAAAGTTAAAAGTTGT CAAAAAA C RAB21 Ensembl:ENSG00000080371 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1265548645 Functional Loss DEL dbSNP153 29..34 33 - - - 5617 RMVar_ID_5617 Human_SNP_ID_506174749 A-to-I Human chr12 + 71798197 71798197 71798197 CCTCTGCCTCCCAGGTTCAAGCAATTATTCCTACCTTAGCCTCCCAAGTAGCTGGGACTACAGGT CCTCTGCCTCCCAGGTTCAAGCAATTATTCCTGCCTTAGCCTCCCAAGTAGCTGGGACTACAGGT A G RAB21 Ensembl:ENSG00000080371 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1476894262 Functional Loss SNV dbSNP153 33..33 33 - - - 5618 RMVar_ID_5618 Human_SNP_ID_506199639 A-to-I Human chr12 + 71899922 71899922 71899922 TTGAGGCCACAGTGAGCTGCGATTGTGCCACTACACTCCGGCCTGGGTGACAGAGCGAGACCCCT TTGAGGCCACAGTGAGCTGCGATTGTGCCACTGCACTCCGGCCTGGGTGACAGAGCGAGACCCCT A G TBC1D15 Ensembl:ENSG00000121749 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1489389893 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25002955 RMVar_hsa_circ_4012,RMVar_hsa_circ_65635,RMVar_hsa_circ_66292,RMVar_hsa_circ_70523,RMVar_hsa_circ_10631,RMVar_hsa_circ_332293,RMVar_hsa_circ_72837,RMVar_hsa_circ_158300,RMVar_hsa_circ_21787,RMVar_hsa_circ_342324,RMVar_hsa_circ_47428,RMVar_hsa_circ_36822,RMVar_hsa_circ_70329 5619 RMVar_ID_5619 Human_SNP_ID_506205608 A-to-I Human chr12 + 71924378 71924374 71924378 AGTCTGCTTTTTTAAAATTTTTTTTCTTGAGAAAGAGTCTTGCTCTGTTGCCCAGGCTGGAGTGC AGTCTGCTTTTTTAAAATTTTTTTTCTTG____AGAGTCTTGCTCTGTTGCCCAGGCTGGAGTGC GAGAA G TBC1D15 Ensembl:ENSG00000121749 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1249620644 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_2368872 5620 RMVar_ID_5620 Human_SNP_ID_506205610 A-to-I Human chr12 + 71924378 71924378 71924378 AGTCTGCTTTTTTAAAATTTTTTTTCTTGAGAAAGAGTCTTGCTCTGTTGCCCAGGCTGGAGTGC AGTCTGCTTTTTTAAAATTTTTTTTCTTGAGAGAGAGTCTTGCTCTGTTGCCCAGGCTGGAGTGC A G TBC1D15 Ensembl:ENSG00000121749 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1011909596 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2368872 5621 RMVar_ID_5621 Human_SNP_ID_507006273 A-to-I Human chr12 - 75111210 75111210 75111210 GAGGGTGAAGAATACATGCACTCTAACATATTATCTTCCTTTATGAACACAGAGAATTACAGCAC GAGGGTGAAGAATACATGCACTCTAACATATTGTCTTCCTTTATGAACACAGAGAATTACAGCAC T C KCNC2 Ensembl:ENSG00000166006 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1206260525 Functional Loss SNV dbSNP153 33..33 33 - - - 5622 RMVar_ID_5622 Human_SNP_ID_507073896 A-to-I Human chr12 - 75382557 75382557 75382557 TGGCTTACAGCAACCTCCGCTTCTTGGGTTCAAGTGATTCTCATGACTCAGCCTCCTGAGTAGCT TGGCTTACAGCAACCTCCGCTTCTTGGGTTCAGGTGATTCTCATGACTCAGCCTCCTGAGTAGCT T C CAPS2 Ensembl:ENSG00000180881 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1259713076 Functional Loss SNV dbSNP153 33..33 33 - - - 5623 RMVar_ID_5623 Human_SNP_ID_507101687 A-to-I Human chr12 - 75496101 75496101 75496101 TACTTGGGAGGCTGAGGCAGGAGGATCGCCTGAACCCGTGAGATGGAGGTTGCAGTGAGCTGAGA TACTTGGGAGGCTGAGGCAGGAGGATCGCCTGTACCCGTGAGATGGAGGTTGCAGTGAGCTGAGA T A KRR1 Ensembl:ENSG00000111615 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs1391787938 Functional Loss SNV dbSNP153 33..33 33 - - - 5624 RMVar_ID_5624 Human_SNP_ID_507101729 A-to-I Human chr12 - 75496292 75496292 75496292 GGAGTGCAGTGGTACAATCTCTGCTCACTGCAACCTCCACCTCCTGGGCTCAAGTGATTGTCCTG GGAGTGCAGTGGTACAATCTCTGCTCACTGCAGCCTCCACCTCCTGGGCTCAAGTGATTGTCCTG T C KRR1 Ensembl:ENSG00000111615 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs983292192 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_866653 5625 RMVar_ID_5625 Human_SNP_ID_507236641 A-to-I Human chr12 - 76051578 76051578 76051578 GAAGGATCACTTGAGGCCAGCCTGGGCAACATAGCGAGACCCTGTCTCTAAAAAAGAAAAGTGCT GAAGGATCACTTGAGGCCAGCCTGGGCAACATGGCGAGACCCTGTCTCTAAAAAAGAAAAGTGCT T C NAP1L1 Ensembl:ENSG00000187109 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1317087961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25003497 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_105090,RMVar_hsa_circ_158352,RMVar_hsa_circ_30780,RMVar_hsa_circ_125978,RMVar_hsa_circ_77163,RMVar_hsa_circ_80567,RMVar_hsa_circ_158354,RMVar_hsa_circ_158355,RMVar_hsa_circ_158356,RMVar_hsa_circ_158353,RMVar_hsa_circ_83129,RMVar_hsa_circ_117311,RMVar_hsa_circ_41971,RMVar_hsa_circ_127945,RMVar_hsa_circ_158358,RMVar_hsa_circ_158359,RMVar_hsa_circ_158357,RMVar_hsa_circ_78378,RMVar_hsa_circ_158360,RMVar_hsa_circ_158361 5626 RMVar_ID_5626 Human_SNP_ID_507238087 A-to-I Human chr12 - 76057210 76057210 76057210 TCTTGGCTCACTGCAGCTCATTCCTGGGCCCAAGCTATTCTCCCACCTCAGCCTCCCAAGTTGCT TCTTGGCTCACTGCAGCTCATTCCTGGGCCCAGGCTATTCTCCCACCTCAGCCTCCCAAGTTGCT T C NAP1L1 Ensembl:ENSG00000187109 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1291235783 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12035229 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_41971,RMVar_hsa_circ_158357,RMVar_hsa_circ_78378,RMVar_hsa_circ_40655,RMVar_hsa_circ_158361,RMVar_hsa_circ_303154,RMVar_hsa_circ_351187,RMVar_hsa_circ_16718 5627 RMVar_ID_5627 Human_SNP_ID_507238222 A-to-I Human chr12 + 76057731 76057731 76057731 ACAATGATTAGAGAAGAATTTTCCAAATGAATATGCAAAACTTACTGTGGAAAATTCACCCAAAC ACAATGATTAGAGAAGAATTTTCCAAATGAATTTGCAAAACTTACTGTGGAAAATTCACCCAAAC A T AC011611.5 Ensembl:ENSG00000257941 Pseudogene exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs878942714 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1874891 5628 RMVar_ID_5628 Human_SNP_ID_507243285 A-to-I Human chr12 - 76076831 76076831 76076831 GAGCAATAGTCTATATCATAGCCTAGGTGCGTAGTAGGCTATACCATCTAGGTTTGTGTAAGTAT GAGCAATAGTCTATATCATAGCCTAGGTGCGTCGTAGGCTATACCATCTAGGTTTGTGTAAGTAT T G NAP1L1 Ensembl:ENSG00000187109 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1277292375 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12036204,Human_RBP_ID_17561217 RMVar_hsa_circ_268347 5629 RMVar_ID_5629 Human_SNP_ID_507243292 A-to-I Human chr12 - 76076870 76076870 76076870 ATTCAATACAGTCACATGCTGTATAGGTGTGTAGCCTGGGAGCAATAGTCTATATCATAGCCTAG ATTCAATACAGTCACATGCTGTATAGGTGTGTGGCCTGGGAGCAATAGTCTATATCATAGCCTAG T C NAP1L1 Ensembl:ENSG00000187109 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs914015894 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12036205,Human_RBP_ID_17561217 RMVar_hsa_circ_268347 5630 RMVar_ID_5630 Human_SNP_ID_507243296 A-to-I Human chr12 - 76076893 76076893 76076893 ATTATATTAAAGTTGCCTATGGTATTCAATACAGTCACATGCTGTATAGGTGTGTAGCCTGGGAG ATTATATTAAAGTTGCCTATGGTATTCAATACGGTCACATGCTGTATAGGTGTGTAGCCTGGGAG T C NAP1L1 Ensembl:ENSG00000187109 Protein coding intron GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;ASD brains,temporal_cortex;Bronchiolar epithelium,BEP2D cell line - 29129909,30559470,31158229 RNA-Seq:(High) rs1022255398 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6222450,Human_RBP_ID_17561217 RMVar_hsa_circ_268347 5631 RMVar_ID_5631 Human_SNP_ID_507243927 A-to-I Human chr12 - 76079269 76079269 76079269 CTCCTGCCCCAGCCTTCCAAAGTGCTGAGACTATAGACGTGAGCTACCGCACATGGCCTCACCTT CTCCTGCCCCAGCCTTCCAAAGTGCTGAGACTGTAGACGTGAGCTACCGCACATGGCCTCACCTT T C NAP1L1 Ensembl:ENSG00000187109 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1340088870 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6222507,Human_RBP_ID_8384011,Human_RBP_ID_12036367,Human_RBP_ID_25004120 RMVar_hsa_circ_268347 5632 RMVar_ID_5632 Human_SNP_ID_507244083 A-to-I Human chr12 - 76079808 76079808 76079808 TGGAGAATGCATACCTGTAGTCCCAGCTACTCAGGAGGCTGAGGTGAGAGGATCACTTGAGCCTG TGGAGAATGCATACCTGTAGTCCCAGCTACTCGGGAGGCTGAGGTGAGAGGATCACTTGAGCCTG T C NAP1L1 Ensembl:ENSG00000187109 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1138894 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17112160,Human_RBP_ID_17561218 RMVar_hsa_circ_268347 5633 RMVar_ID_5633 Human_SNP_ID_507337378 A-to-I Human chr12 - 76450875 76450875 76450875 CGCCAACCAAAGATTTGCATCAGCCATCTCTTAGTCCAGCAAGTCCTCATAGCCAGGGTAGGAAG CGCCAACCAAAGATTTGCATCAGCCATCTCTTCGTCCAGCAAGTCCTCATAGCCAGGGTAGGAAG T G OSBPL8 Ensembl:ENSG00000091039 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1400659878 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_33753,Human_RBP_ID_17827264,Human_RBP_ID_26323175 Human_Splice_Rec_1401019,Human_Splice_Rec_1401065,Human_Splice_Rec_1401111,Human_Splice_Rec_1401155,Human_Splice_Rec_1401205,Human_Splice_Rec_1401283,Human_Splice_Rec_1401295,Human_Splice_Rec_1401307 Human_miRNA_ID_1962301,Human_miRNA_ID_2542062,Human_miRNA_ID_2543932,Human_miRNA_ID_2545782,Human_miRNA_ID_2547636,Human_miRNA_ID_2549500,Human_miRNA_ID_2551369,Human_miRNA_ID_2556780,Human_miRNA_ID_2558663,Human_miRNA_ID_2589081 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_279309,RMVar_hsa_circ_44360,RMVar_hsa_circ_20034,RMVar_hsa_circ_304652,RMVar_hsa_circ_342160,RMVar_hsa_circ_158379,RMVar_hsa_circ_26827,RMVar_hsa_circ_158378 5634 RMVar_ID_5634 Human_SNP_ID_507355699 A-to-I Human chr12 - 76526774 76526774 76526774 TGGTGGTGCACGCCTGTAATCCCAGCTACTTGAGAGACTGAGACAGGAGAGTTGCTGGAACCCGG TGGTGGTGCACGCCTGTAATCCCAGCTACTTGGGAGACTGAGACAGGAGAGTTGCTGGAACCCGG T C OSBPL8 Ensembl:ENSG00000091039 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270366835 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_115482 RMVar_hsa_circ_342160,RMVar_hsa_circ_26827,RMVar_hsa_circ_319806 5635 RMVar_ID_5635 Human_SNP_ID_507356588 A-to-I Human chr12 - 76530132 76530132 76530132 TGAGGATCCCTTGTTTCCAATAGTTTGAGATTATAGTGAACTATGATCTTGCCACCACACTCCTG TGAGGATCCCTTGTTTCCAATAGTTTGAGATTCTAGTGAACTATGATCTTGCCACCACACTCCTG T G OSBPL8 Ensembl:ENSG00000091039 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1321057682 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_342160,RMVar_hsa_circ_26827,RMVar_hsa_circ_319806 5636 RMVar_ID_5636 Human_SNP_ID_507361237 A-to-I Human chr12 - 76549539 76549539 76549539 GGGCATGGTGGCAGGTGCCTGTAATCCCAGCTACTTAGGAGTCTGAGGCAGGAGAATCACTTGAA GGGCATGGTGGCAGGTGCCTGTAATCCCAGCTGCTTAGGAGTCTGAGGCAGGAGAATCACTTGAA T C OSBPL8 Ensembl:ENSG00000091039 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1336487226 Functional Loss SNV dbSNP153 33..33 33 - - - 5637 RMVar_ID_5637 Human_SNP_ID_507429903 A-to-I Human chr12 + 76831780 76831780 76831780 GTGATCCTCCCACCTCAGCCTCCTGAGAAGCTAGGACTACAGGCACAAGCCACCATGCCTGGCTA GTGATCCTCCCACCTCAGCCTCCTGAGAAGCTGGGACTACAGGCACAAGCCACCATGCCTGGCTA A G ZDHHC17 Ensembl:ENSG00000186908 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1288937977 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12038160 RMVar_hsa_circ_341680,RMVar_hsa_circ_82543,RMVar_hsa_circ_58010,RMVar_hsa_circ_1172,RMVar_hsa_circ_158388,RMVar_hsa_circ_265737,RMVar_hsa_circ_301033,RMVar_hsa_circ_356659 5638 RMVar_ID_5638 Human_SNP_ID_507429904 A-to-I Human chr12 + 76831794 76831794 76831794 TCAGCCTCCTGAGAAGCTAGGACTACAGGCACAAGCCACCATGCCTGGCTAATTTGCGTATTTTT TCAGCCTCCTGAGAAGCTAGGACTACAGGCACGAGCCACCATGCCTGGCTAATTTGCGTATTTTT A G ZDHHC17 Ensembl:ENSG00000186908 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1157110328 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_341680,RMVar_hsa_circ_82543,RMVar_hsa_circ_58010,RMVar_hsa_circ_1172,RMVar_hsa_circ_158388,RMVar_hsa_circ_265737,RMVar_hsa_circ_301033,RMVar_hsa_circ_356659 5639 RMVar_ID_5639 Human_SNP_ID_507431227 A-to-I Human chr12 + 76837261 76837261 76837261 AGGTTCAGGTGGCTCTTGTGCCTCAGACTCTCAAGTAGCTAGGATTACAGGCATGTGCCACCACA AGGTTCAGGTGGCTCTTGTGCCTCAGACTCTCCAGTAGCTAGGATTACAGGCATGTGCCACCACA A C ZDHHC17 Ensembl:ENSG00000186908 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs888069711 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_341680,RMVar_hsa_circ_82543,RMVar_hsa_circ_58010,RMVar_hsa_circ_1172,RMVar_hsa_circ_158388,RMVar_hsa_circ_265737,RMVar_hsa_circ_301033,RMVar_hsa_circ_356659 5640 RMVar_ID_5640 Human_SNP_ID_507431231 A-to-I Human chr12 + 76837277 76837277 76837277 TGTGCCTCAGACTCTCAAGTAGCTAGGATTACAGGCATGTGCCACCACACCTGGCTATTTTCTAT TGTGCCTCAGACTCTCAAGTAGCTAGGATTACGGGCATGTGCCACCACACCTGGCTATTTTCTAT A G ZDHHC17 Ensembl:ENSG00000186908 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1487227562 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_341680,RMVar_hsa_circ_82543,RMVar_hsa_circ_58010,RMVar_hsa_circ_1172,RMVar_hsa_circ_158388,RMVar_hsa_circ_265737,RMVar_hsa_circ_301033,RMVar_hsa_circ_356659 5641 RMVar_ID_5641 Human_SNP_ID_507503144 A-to-I Human chr12 - 77143114 77143114 77143114 GGGTTCGGGTGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGACATGCACCACCATG GGGTTCGGGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGACATGCACCACCATG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1003672357 Functional Loss SNV dbSNP153 33..33 33 - - - 5642 RMVar_ID_5642 Human_SNP_ID_507952114 A-to-I Human chr12 + 78946501 78946501 78946501 ACAAGGCAAAACTGCATCTTTACTAAAAATACAGAAATTAGCCAGGTGTGGTGGCACACACCTGC ACAAGGCAAAACTGCATCTTTACTAAAAATACTGAAATTAGCCAGGTGTGGTGGCACACACCTGC A T SYT1 Ensembl:ENSG00000067715 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1222107863 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51947,RMVar_hsa_circ_324820,RMVar_hsa_circ_333141,RMVar_hsa_circ_21325,RMVar_hsa_circ_47417,RMVar_hsa_circ_287301,RMVar_hsa_circ_307887,RMVar_hsa_circ_158485,RMVar_hsa_circ_158486,RMVar_hsa_circ_158484,RMVar_hsa_circ_158487 5643 RMVar_ID_5643 Human_SNP_ID_507995185 A-to-I Human chr12 + 79126390 79126390 79126390 TCAAACAATTCTCCTGCCTCAGCCTCCAGAGTAGCTGGGATTGCAGGCATGTGCCACCACACCTA TCAAACAATTCTCCTGCCTCAGCCTCCAGAGTGGCTGGGATTGCAGGCATGTGCCACCACACCTA A G SYT1 Ensembl:ENSG00000067715 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1019334216 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36430,RMVar_hsa_circ_51947,RMVar_hsa_circ_333141,RMVar_hsa_circ_47417,RMVar_hsa_circ_343651,RMVar_hsa_circ_42570,RMVar_hsa_circ_308387,RMVar_hsa_circ_74479 5644 RMVar_ID_5644 Human_SNP_ID_507995679 A-to-I Human chr12 + 79128726 79128726 79128726 GTGCAACAAACCACCATGGCACGTGTATACCTATGTAATAAACCTGCACGTTCTGCACATGTATC GTGCAACAAACCACCATGGCACGTGTATACCTTTGTAATAAACCTGCACGTTCTGCACATGTATC A T SYT1 Ensembl:ENSG00000067715 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1401237851 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36430,RMVar_hsa_circ_51947,RMVar_hsa_circ_333141,RMVar_hsa_circ_47417,RMVar_hsa_circ_343651,RMVar_hsa_circ_42570,RMVar_hsa_circ_308387,RMVar_hsa_circ_74479 5645 RMVar_ID_5645 Human_SNP_ID_507996497 A-to-I Human chr12 + 79132338 79132338 79132338 TGGTATGGTGGCACGTGCCTGTCGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCGTTTGAA TGGTATGGTGGCACGTGCCTGTCGTCCCAGCTCCTCAGGAGGCTGAGGCAGGAGAATCGTTTGAA A C SYT1 Ensembl:ENSG00000067715 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs576299848 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36430,RMVar_hsa_circ_51947,RMVar_hsa_circ_333141,RMVar_hsa_circ_47417,RMVar_hsa_circ_343651,RMVar_hsa_circ_42570,RMVar_hsa_circ_308387,RMVar_hsa_circ_74479 5646 RMVar_ID_5646 Human_SNP_ID_508095102 A-to-I Human chr12 - 79552951 79552951 79552951 AGAAGGAACAAACTCCGGACACGCCATCTTTAAGAACTGTAACACTTACCACGAGGGTCCGCGGC AGAAGGAACAAACTCCGGACACGCCATCTTTAGGAACTGTAACACTTACCACGAGGGTCCGCGGC T C lnc-PAWR-7 RNACentral:URS00008C1D46 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1229344144 Functional Loss SNV dbSNP153 33..33 33 - - - 5647 RMVar_ID_5647 Human_SNP_ID_508097106 A-to-I Human chr12 - 79560979 79560977 79560980 AACTGTAGACAAGAAATCCAGCCAGGCACAGTAGCTCACTACTGTAATCCCAGCACTTTGGGAGG AACTGTAGACAAGAAATCCAGCCAGGCACAG___CTCACTACTGTAATCCCAGCACTTTGGGAGG GCTA G lnc-PAWR-7 RNACentral:URS00008C1D46 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1423708506 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_2357826,Human_RBP_ID_12040714 5648 RMVar_ID_5648 Human_SNP_ID_508098044 A-to-I Human chr12 - 79563980 79563980 79563980 TTTTGTAGAGTTGGGGTTTCCCCTTGTTGCCCAGGCTGGTTTTGAACTCCTGAGCTCAAGCAATC TTTTGTAGAGTTGGGGTTTCCCCTTGTTGCCCGGGCTGGTTTTGAACTCCTGAGCTCAAGCAATC T C lnc-PAWR-7 RNACentral:URS00008C1D46 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs762215214 Functional Loss SNV dbSNP153 33..33 33 - - - 5649 RMVar_ID_5649 Human_SNP_ID_508105614 A-to-I Human chr12 - 79594754 79594753 79594755 CAAGGTGCCATTGCACTCCAGCCTGGGTGACAAGAGTGAAACACTGCCATACATACATACACACA CAAGGTGCCATTGCACTCCAGCCTGGGTGAC__GAGTGAAACACTGCCATACATACATACACACA CTT C PAWR Ensembl:ENSG00000177425 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs199967882 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_158506,RMVar_hsa_circ_158507,RMVar_hsa_circ_344629,RMVar_hsa_circ_354315,RMVar_hsa_circ_359912 5650 RMVar_ID_5650 Human_SNP_ID_508106933 A-to-I Human chr12 - 79600658 79600648 79600659 ATAGTAAGACACGTCTCTACAAAAAAAAAAAAAAAAAAAAAAGCCAGGTATGGTGGTGGCATATG ATAGTAAGACACGTCTCTACAAAAAAAAAAA___________GCCAGGTATGGTGGTGGCATATG CTTTTTTTTTTT C PAWR Ensembl:ENSG00000177425 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1025749975 Functional Loss DEL dbSNP153 32..42 33 - - - RMVar_hsa_circ_68261,RMVar_hsa_circ_158507,RMVar_hsa_circ_354315 5651 RMVar_ID_5651 Human_SNP_ID_508106934 A-to-I Human chr12 - 79600658 79600648 79600659 ATAGTAAGACACGTCTCTACAAAAAAAAAAAAAAAAAAAAAAGCCAGGTATGGTGGTGGCATATG ATAGTAAGACACGTCTCTACAAAAAAAAAAA__________AGCCAGGTATGGTGGTGGCATATG CTTTTTTTTTTT CT PAWR Ensembl:ENSG00000177425 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1025749975 Functional Loss DEL dbSNP153 32..41 33 - - - RMVar_hsa_circ_68261,RMVar_hsa_circ_158507,RMVar_hsa_circ_354315 5652 RMVar_ID_5652 Human_SNP_ID_508106935 A-to-I Human chr12 - 79600658 79600648 79600659 ATAGTAAGACACGTCTCTACAAAAAAAAAAAAAAAAAAAAAAGCCAGGTATGGTGGTGGCATATG ATAGTAAGACACGTCTCTACAAAAAAAAAAA_______AAAAGCCAGGTATGGTGGTGGCATATG CTTTTTTTTTTT CTTTT PAWR Ensembl:ENSG00000177425 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1025749975 Functional Loss DEL dbSNP153 32..38 33 - - - RMVar_hsa_circ_68261,RMVar_hsa_circ_158507,RMVar_hsa_circ_354315 5653 RMVar_ID_5653 Human_SNP_ID_508106936 A-to-I Human chr12 - 79600658 79600648 79600659 ATAGTAAGACACGTCTCTACAAAAAAAAAAAAAAAAAAAAAAGCCAGGTATGGTGGTGGCATATG ATAGTAAGACACGTCTCTACAAAAAAAAAAA______AAAAAGCCAGGTATGGTGGTGGCATATG CTTTTTTTTTTT CTTTTT PAWR Ensembl:ENSG00000177425 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1025749975 Functional Loss DEL dbSNP153 32..37 33 - - - RMVar_hsa_circ_68261,RMVar_hsa_circ_158507,RMVar_hsa_circ_354315 5654 RMVar_ID_5654 Human_SNP_ID_508106937 A-to-I Human chr12 - 79600658 79600648 79600659 ATAGTAAGACACGTCTCTACAAAAAAAAAAAAAAAAAAAAAAGCCAGGTATGGTGGTGGCATATG ATAGTAAGACACGTCTCTACAAAAAAAAAAA_____AAAAAAGCCAGGTATGGTGGTGGCATATG CTTTTTTTTTTT CTTTTTT PAWR Ensembl:ENSG00000177425 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1025749975 Functional Loss DEL dbSNP153 32..36 33 - - - RMVar_hsa_circ_68261,RMVar_hsa_circ_158507,RMVar_hsa_circ_354315 5655 RMVar_ID_5655 Human_SNP_ID_508106938 A-to-I Human chr12 - 79600658 79600648 79600659 ATAGTAAGACACGTCTCTACAAAAAAAAAAAAAAAAAAAAAAGCCAGGTATGGTGGTGGCATATG ATAGTAAGACACGTCTCTACAAAAAAAAAAA____AAAAAAAGCCAGGTATGGTGGTGGCATATG CTTTTTTTTTTT CTTTTTTT PAWR Ensembl:ENSG00000177425 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1025749975 Functional Loss DEL dbSNP153 32..35 33 - - - RMVar_hsa_circ_68261,RMVar_hsa_circ_158507,RMVar_hsa_circ_354315 5656 RMVar_ID_5656 Human_SNP_ID_508106939 A-to-I Human chr12 - 79600658 79600648 79600659 ATAGTAAGACACGTCTCTACAAAAAAAAAAAAAAAAAAAAAAGCCAGGTATGGTGGTGGCATATG ATAGTAAGACACGTCTCTACAAAAAAAAAAA___AAAAAAAAGCCAGGTATGGTGGTGGCATATG CTTTTTTTTTTT CTTTTTTTT PAWR Ensembl:ENSG00000177425 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1025749975 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_68261,RMVar_hsa_circ_158507,RMVar_hsa_circ_354315 5657 RMVar_ID_5657 Human_SNP_ID_508106940 A-to-I Human chr12 - 79600658 79600648 79600659 ATAGTAAGACACGTCTCTACAAAAAAAAAAAAAAAAAAAAAAGCCAGGTATGGTGGTGGCATATG ATAGTAAGACACGTCTCTACAAAAAAAAAAA__AAAAAAAAAGCCAGGTATGGTGGTGGCATATG CTTTTTTTTTTT CTTTTTTTTT PAWR Ensembl:ENSG00000177425 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1025749975 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_68261,RMVar_hsa_circ_158507,RMVar_hsa_circ_354315 5658 RMVar_ID_5658 Human_SNP_ID_508107442 A-to-I Human chr12 - 79602778 79602770 79602778 AACATAGTGACACGTCTCTACAAAAAAAAAAAAAAAAAAATTAGCCAGGTATGGTGGCATATGCC AACATAGTGACACGTCTCTACAAAAAAAAAAA________TTAGCCAGGTATGGTGGCATATGCC ATTTTTTTT A PAWR Ensembl:ENSG00000177425 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1037453130 Functional Loss DEL dbSNP153 33..40 33 - - - RMVar_hsa_circ_68261,RMVar_hsa_circ_158507,RMVar_hsa_circ_354315 5659 RMVar_ID_5659 Human_SNP_ID_508107442 A-to-I Human chr12 - 79602777 79602770 79602778 ACATAGTGACACGTCTCTACAAAAAAAAAAAAAAAAAAATTAGCCAGGTATGGTGGCATATGCCT ACATAGTGACACGTCTCTACAAAAAAAAAAA________TTAGCCAGGTATGGTGGCATATGCCT ATTTTTTTT A PAWR Ensembl:ENSG00000177425 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1037453130 Functional Loss DEL dbSNP153 32..39 33 - - - RMVar_hsa_circ_68261,RMVar_hsa_circ_158507,RMVar_hsa_circ_354315 5660 RMVar_ID_5660 Human_SNP_ID_508107443 A-to-I Human chr12 - 79602778 79602770 79602778 AACATAGTGACACGTCTCTACAAAAAAAAAAAAAAAAAAATTAGCCAGGTATGGTGGCATATGCC AACATAGTGACACGTCTCTACAAAAAAAAAAA_______ATTAGCCAGGTATGGTGGCATATGCC ATTTTTTTT AT PAWR Ensembl:ENSG00000177425 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1037453130 Functional Loss DEL dbSNP153 33..39 33 - - - RMVar_hsa_circ_68261,RMVar_hsa_circ_158507,RMVar_hsa_circ_354315 5661 RMVar_ID_5661 Human_SNP_ID_508107443 A-to-I Human chr12 - 79602777 79602770 79602778 ACATAGTGACACGTCTCTACAAAAAAAAAAAAAAAAAAATTAGCCAGGTATGGTGGCATATGCCT ACATAGTGACACGTCTCTACAAAAAAAAAAA_______ATTAGCCAGGTATGGTGGCATATGCCT ATTTTTTTT AT PAWR Ensembl:ENSG00000177425 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1037453130 Functional Loss DEL dbSNP153 32..38 33 - - - RMVar_hsa_circ_68261,RMVar_hsa_circ_158507,RMVar_hsa_circ_354315 5662 RMVar_ID_5662 Human_SNP_ID_508107444 A-to-I Human chr12 - 79602778 79602770 79602778 AACATAGTGACACGTCTCTACAAAAAAAAAAAAAAAAAAATTAGCCAGGTATGGTGGCATATGCC AACATAGTGACACGTCTCTACAAAAAAAAAAA______AATTAGCCAGGTATGGTGGCATATGCC ATTTTTTTT ATT PAWR Ensembl:ENSG00000177425 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1037453130 Functional Loss DEL dbSNP153 33..38 33 - - - RMVar_hsa_circ_68261,RMVar_hsa_circ_158507,RMVar_hsa_circ_354315 5663 RMVar_ID_5663 Human_SNP_ID_508107444 A-to-I Human chr12 - 79602777 79602770 79602778 ACATAGTGACACGTCTCTACAAAAAAAAAAAAAAAAAAATTAGCCAGGTATGGTGGCATATGCCT ACATAGTGACACGTCTCTACAAAAAAAAAAA______AATTAGCCAGGTATGGTGGCATATGCCT ATTTTTTTT ATT PAWR Ensembl:ENSG00000177425 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1037453130 Functional Loss DEL dbSNP153 32..37 33 - - - RMVar_hsa_circ_68261,RMVar_hsa_circ_158507,RMVar_hsa_circ_354315 5664 RMVar_ID_5664 Human_SNP_ID_508107445 A-to-I Human chr12 - 79602778 79602770 79602778 AACATAGTGACACGTCTCTACAAAAAAAAAAAAAAAAAAATTAGCCAGGTATGGTGGCATATGCC AACATAGTGACACGTCTCTACAAAAAAAAAAA_____AAATTAGCCAGGTATGGTGGCATATGCC ATTTTTTTT ATTT PAWR Ensembl:ENSG00000177425 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1037453130 Functional Loss DEL dbSNP153 33..37 33 - - - RMVar_hsa_circ_68261,RMVar_hsa_circ_158507,RMVar_hsa_circ_354315 5665 RMVar_ID_5665 Human_SNP_ID_508107445 A-to-I Human chr12 - 79602777 79602770 79602778 ACATAGTGACACGTCTCTACAAAAAAAAAAAAAAAAAAATTAGCCAGGTATGGTGGCATATGCCT ACATAGTGACACGTCTCTACAAAAAAAAAAA_____AAATTAGCCAGGTATGGTGGCATATGCCT ATTTTTTTT ATTT PAWR Ensembl:ENSG00000177425 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1037453130 Functional Loss DEL dbSNP153 32..36 33 - - - RMVar_hsa_circ_68261,RMVar_hsa_circ_158507,RMVar_hsa_circ_354315 5666 RMVar_ID_5666 Human_SNP_ID_508107446 A-to-I Human chr12 - 79602778 79602770 79602778 AACATAGTGACACGTCTCTACAAAAAAAAAAAAAAAAAAATTAGCCAGGTATGGTGGCATATGCC AACATAGTGACACGTCTCTACAAAAAAAAAAA___AAAAATTAGCCAGGTATGGTGGCATATGCC ATTTTTTTT ATTTTT PAWR Ensembl:ENSG00000177425 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1037453130 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_68261,RMVar_hsa_circ_158507,RMVar_hsa_circ_354315 5667 RMVar_ID_5667 Human_SNP_ID_508107446 A-to-I Human chr12 - 79602777 79602770 79602778 ACATAGTGACACGTCTCTACAAAAAAAAAAAAAAAAAAATTAGCCAGGTATGGTGGCATATGCCT ACATAGTGACACGTCTCTACAAAAAAAAAAA___AAAAATTAGCCAGGTATGGTGGCATATGCCT ATTTTTTTT ATTTTT PAWR Ensembl:ENSG00000177425 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1037453130 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_68261,RMVar_hsa_circ_158507,RMVar_hsa_circ_354315 5668 RMVar_ID_5668 Human_SNP_ID_508107447 A-to-I Human chr12 - 79602778 79602770 79602778 AACATAGTGACACGTCTCTACAAAAAAAAAAAAAAAAAAATTAGCCAGGTATGGTGGCATATGCC AACATAGTGACACGTCTCTACAAAAAAAAAAA__AAAAAATTAGCCAGGTATGGTGGCATATGCC ATTTTTTTT ATTTTTT PAWR Ensembl:ENSG00000177425 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1037453130 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_68261,RMVar_hsa_circ_158507,RMVar_hsa_circ_354315 5669 RMVar_ID_5669 Human_SNP_ID_508107447 A-to-I Human chr12 - 79602777 79602770 79602778 ACATAGTGACACGTCTCTACAAAAAAAAAAAAAAAAAAATTAGCCAGGTATGGTGGCATATGCCT ACATAGTGACACGTCTCTACAAAAAAAAAAA__AAAAAATTAGCCAGGTATGGTGGCATATGCCT ATTTTTTTT ATTTTTT PAWR Ensembl:ENSG00000177425 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1037453130 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_68261,RMVar_hsa_circ_158507,RMVar_hsa_circ_354315 5670 RMVar_ID_5670 Human_SNP_ID_508107448 A-to-I Human chr12 - 79602778 79602770 79602778 AACATAGTGACACGTCTCTACAAAAAAAAAAAAAAAAAAATTAGCCAGGTATGGTGGCATATGCC AACATAGTGACACGTCTCTACAAAAAAAAAAA_AAAAAAATTAGCCAGGTATGGTGGCATATGCC ATTTTTTTT ATTTTTTT PAWR Ensembl:ENSG00000177425 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1037453130 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_68261,RMVar_hsa_circ_158507,RMVar_hsa_circ_354315 5671 RMVar_ID_5671 Human_SNP_ID_508107514 A-to-I Human chr12 - 79603050 79603050 79603050 TTTTATAGAGACAGAGTCTCATTATGTTGTCCAGACTGGTCTTGAACTCCTGGACCTAAGCAGTC TTTTATAGAGACAGAGTCTCATTATGTTGTCCCGACTGGTCTTGAACTCCTGGACCTAAGCAGTC T G PAWR Ensembl:ENSG00000177425 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1422291233 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17561221 RMVar_hsa_circ_68261,RMVar_hsa_circ_158507,RMVar_hsa_circ_354315 5672 RMVar_ID_5672 Human_SNP_ID_508107522 A-to-I Human chr12 - 79603078 79603078 79603078 ATGCCTGACTAATTTTTTATTTTTTTAATTTTATAGAGACAGAGTCTCATTATGTTGTCCAGACT ATGCCTGACTAATTTTTTATTTTTTTAATTTTGTAGAGACAGAGTCTCATTATGTTGTCCAGACT T C PAWR Ensembl:ENSG00000177425 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs908120336 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6251908,Human_RBP_ID_12041851,Human_RBP_ID_17561221 RMVar_hsa_circ_68261,RMVar_hsa_circ_158507,RMVar_hsa_circ_354315 5673 RMVar_ID_5673 Human_SNP_ID_508107524 A-to-I Human chr12 - 79603092 79603085 79603092 AGGAACATGCCACCATGCCTGACTAATTTTTTATTTTTTTAATTTTATAGAGACAGAGTCTCATT AGGAACATGCCACCATGCCTGACTAATTTTTT_______TAATTTTATAGAGACAGAGTCTCATT AAAAAAAT A PAWR Ensembl:ENSG00000177425 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251413181 Functional Loss DEL dbSNP153 33..39 33 - - - Human_RBP_ID_6251908 RMVar_hsa_circ_68261,RMVar_hsa_circ_158507,RMVar_hsa_circ_354315 5674 RMVar_ID_5674 Human_SNP_ID_508107528 A-to-I Human chr12 - 79603092 79603092 79603092 AGGAACATGCCACCATGCCTGACTAATTTTTTATTTTTTTAATTTTATAGAGACAGAGTCTCATT AGGAACATGCCACCATGCCTGACTAATTTTTTTTTTTTTTAATTTTATAGAGACAGAGTCTCATT T A PAWR Ensembl:ENSG00000177425 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1565998279 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6251908 RMVar_hsa_circ_68261,RMVar_hsa_circ_158507,RMVar_hsa_circ_354315 5675 RMVar_ID_5675 Human_SNP_ID_508107533 A-to-I Human chr12 - 79603113 79603113 79603113 GTCCCAAGTGCTTGGGACTCCAGGAACATGCCACCATGCCTGACTAATTTTTTATTTTTTTAATT GTCCCAAGTGCTTGGGACTCCAGGAACATGCCGCCATGCCTGACTAATTTTTTATTTTTTTAATT T C PAWR Ensembl:ENSG00000177425 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs543775000 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6225088 RMVar_hsa_circ_68261,RMVar_hsa_circ_158507,RMVar_hsa_circ_354315 5676 RMVar_ID_5676 Human_SNP_ID_508111321 A-to-I Human chr12 - 79618189 79618189 79618189 TGGAGGCGGATGTTGCAGTCAGCTGAGATCACACCACTGCATTCCAGCCTGGGTGACAGCGAGAC TGGAGGCGGATGTTGCAGTCAGCTGAGATCACGCCACTGCATTCCAGCCTGGGTGACAGCGAGAC T C PAWR Ensembl:ENSG00000177425 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1361750185 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12042077 RMVar_hsa_circ_158507,RMVar_hsa_circ_354315,RMVar_hsa_circ_295027 5677 RMVar_ID_5677 Human_SNP_ID_508115300 A-to-I Human chr12 - 79632644 79632644 79632644 GCCAGGCTGGGCACATGGTATGCTGCACGCCTATAATCCCAGAACTTTGTGAGACTGAGGCAGGT GCCAGGCTGGGCACATGGTATGCTGCACGCCTGTAATCCCAGAACTTTGTGAGACTGAGGCAGGT T C PAWR Ensembl:ENSG00000177425 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs771573067 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12042150 5678 RMVar_ID_5678 Human_SNP_ID_508117347 A-to-I Human chr12 - 79640082 79640082 79640082 TGGCTAACATGGTGAAACCTTGTCTTTACTAAAAATACAAAAATTAGCCAGGTGTGTTCGCAGGC TGGCTAACATGGTGAAACCTTGTCTTTACTAACAATACAAAAATTAGCCAGGTGTGTTCGCAGGC T G PAWR Ensembl:ENSG00000177425 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs570255121 Functional Loss SNV dbSNP153 33..33 33 - - - 5679 RMVar_ID_5679 Human_SNP_ID_508152932 A-to-I Human chr12 - 79786405 79786405 79786405 ACAGCTACATGATACAAATATGGAACTAACAGATCTTAAATTACAGTTGGAAAAGGCCACCCAGG ACAGCTACATGATACAAATATGGAACTAACAGGTCTTAAATTACAGTTGGAAAAGGCCACCCAGG T C PPP1R12A Ensembl:ENSG00000058272 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1212427839 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1802192,Human_RBP_ID_12043348 Human_Splice_Rec_1402390,Human_Splice_Rec_1402391,Human_Splice_Rec_1402438,Human_Splice_Rec_1402439,Human_Splice_Rec_1402504,Human_Splice_Rec_1402505,Human_Splice_Rec_1402514,Human_Splice_Rec_1402515,Human_Splice_Rec_1402536,Human_Splice_Rec_1402537,Human_Splice_Rec_1402547,Human_Splice_Rec_1402562,Human_Splice_Rec_1402563,Human_Splice_Rec_1402612,Human_Splice_Rec_1402613,Human_Splice_Rec_1402658,Human_Splice_Rec_1402659,Human_Splice_Rec_1402668,Human_Splice_Rec_1402669 RMVar_hsa_circ_40338,RMVar_hsa_circ_64063,RMVar_hsa_circ_84302,RMVar_hsa_circ_158508,RMVar_hsa_circ_158509,RMVar_hsa_circ_67342,RMVar_hsa_circ_295419,RMVar_hsa_circ_338588,RMVar_hsa_circ_158510,RMVar_hsa_circ_280863,RMVar_hsa_circ_370789,RMVar_hsa_circ_49883,RMVar_hsa_circ_158511,RMVar_hsa_circ_33394,RMVar_hsa_circ_158512 5680 RMVar_ID_5680 Human_SNP_ID_508152933 A-to-I Human chr12 - 79786405 79786405 79786405 ACAGCTACATGATACAAATATGGAACTAACAGATCTTAAATTACAGTTGGAAAAGGCCACCCAGG ACAGCTACATGATACAAATATGGAACTAACAGCTCTTAAATTACAGTTGGAAAAGGCCACCCAGG T G PPP1R12A Ensembl:ENSG00000058272 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1212427839 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1802192,Human_RBP_ID_12043348 Human_Splice_Rec_1402390,Human_Splice_Rec_1402391,Human_Splice_Rec_1402438,Human_Splice_Rec_1402439,Human_Splice_Rec_1402504,Human_Splice_Rec_1402505,Human_Splice_Rec_1402514,Human_Splice_Rec_1402515,Human_Splice_Rec_1402536,Human_Splice_Rec_1402537,Human_Splice_Rec_1402547,Human_Splice_Rec_1402562,Human_Splice_Rec_1402563,Human_Splice_Rec_1402612,Human_Splice_Rec_1402613,Human_Splice_Rec_1402658,Human_Splice_Rec_1402659,Human_Splice_Rec_1402668,Human_Splice_Rec_1402669 RMVar_hsa_circ_40338,RMVar_hsa_circ_64063,RMVar_hsa_circ_84302,RMVar_hsa_circ_158508,RMVar_hsa_circ_158509,RMVar_hsa_circ_67342,RMVar_hsa_circ_295419,RMVar_hsa_circ_338588,RMVar_hsa_circ_158510,RMVar_hsa_circ_280863,RMVar_hsa_circ_370789,RMVar_hsa_circ_49883,RMVar_hsa_circ_158511,RMVar_hsa_circ_33394,RMVar_hsa_circ_158512 5681 RMVar_ID_5681 Human_SNP_ID_508155810 A-to-I Human chr12 - 79799227 79799227 79799227 AGAGAATCACTTGAACCCGGGAGGCAGAGGTTACAGTGAGCTGAGATCGCGCCACTGCACTCCAG AGAGAATCACTTGAACCCGGGAGGCAGAGGTTGCAGTGAGCTGAGATCGCGCCACTGCACTCCAG T C PPP1R12A Ensembl:ENSG00000058272 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1362773865 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64063,RMVar_hsa_circ_49883,RMVar_hsa_circ_41937,RMVar_hsa_circ_60026,RMVar_hsa_circ_33394,RMVar_hsa_circ_78609,RMVar_hsa_circ_281167,RMVar_hsa_circ_158514,RMVar_hsa_circ_73583,RMVar_hsa_circ_17268,RMVar_hsa_circ_158515,RMVar_hsa_circ_70468 5682 RMVar_ID_5682 Human_SNP_ID_508155813 A-to-I Human chr12 - 79799234 79799234 79799234 TGAGGTGAGAGAATCACTTGAACCCGGGAGGCAGAGGTTACAGTGAGCTGAGATCGCGCCACTGC TGAGGTGAGAGAATCACTTGAACCCGGGAGGCGGAGGTTACAGTGAGCTGAGATCGCGCCACTGC T C PPP1R12A Ensembl:ENSG00000058272 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1302981731 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64063,RMVar_hsa_circ_49883,RMVar_hsa_circ_41937,RMVar_hsa_circ_60026,RMVar_hsa_circ_33394,RMVar_hsa_circ_78609,RMVar_hsa_circ_281167,RMVar_hsa_circ_158514,RMVar_hsa_circ_73583,RMVar_hsa_circ_17268,RMVar_hsa_circ_158515,RMVar_hsa_circ_70468 5683 RMVar_ID_5683 Human_SNP_ID_508155817 A-to-I Human chr12 - 79799245 79799245 79799245 ACTCAGGAGGCTGAGGTGAGAGAATCACTTGAACCCGGGAGGCAGAGGTTACAGTGAGCTGAGAT ACTCAGGAGGCTGAGGTGAGAGAATCACTTGATCCCGGGAGGCAGAGGTTACAGTGAGCTGAGAT T A PPP1R12A Ensembl:ENSG00000058272 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1438922564 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64063,RMVar_hsa_circ_49883,RMVar_hsa_circ_41937,RMVar_hsa_circ_60026,RMVar_hsa_circ_33394,RMVar_hsa_circ_78609,RMVar_hsa_circ_281167,RMVar_hsa_circ_158514,RMVar_hsa_circ_73583,RMVar_hsa_circ_17268,RMVar_hsa_circ_158515,RMVar_hsa_circ_70468 5684 RMVar_ID_5684 Human_SNP_ID_508155948 A-to-I Human chr12 - 79799789 79799782 79799789 CCCAGGCTGGGCTCGAATTCCTGGGCTCAAGCAATCAGCCTGCTTCAGCCTTCCAATGTGCTGGA CCCAGGCTGGGCTCGAATTCCTGGGCTCAAGC_______CTGCTTCAGCCTTCCAATGTGCTGGA GGCTGATT G PPP1R12A Ensembl:ENSG00000058272 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1173135705 Functional Loss DEL dbSNP153 33..39 33 - - - RMVar_hsa_circ_64063,RMVar_hsa_circ_49883,RMVar_hsa_circ_41937,RMVar_hsa_circ_60026,RMVar_hsa_circ_33394,RMVar_hsa_circ_78609,RMVar_hsa_circ_281167,RMVar_hsa_circ_158514,RMVar_hsa_circ_73583,RMVar_hsa_circ_17268,RMVar_hsa_circ_158515,RMVar_hsa_circ_70468 5685 RMVar_ID_5685 Human_SNP_ID_508155978 A-to-I Human chr12 - 79799897 79799897 79799897 TCAGGTGATCCTCTCATCTCAGCCTCCCGAGTAACTGGGAGTACAGGCATGTGCCACATGCCTGG TCAGGTGATCCTCTCATCTCAGCCTCCCGAGTGACTGGGAGTACAGGCATGTGCCACATGCCTGG T C PPP1R12A Ensembl:ENSG00000058272 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1027337555 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64063,RMVar_hsa_circ_49883,RMVar_hsa_circ_41937,RMVar_hsa_circ_60026,RMVar_hsa_circ_33394,RMVar_hsa_circ_78609,RMVar_hsa_circ_281167,RMVar_hsa_circ_158514,RMVar_hsa_circ_73583,RMVar_hsa_circ_17268,RMVar_hsa_circ_158515,RMVar_hsa_circ_70468 5686 RMVar_ID_5686 Human_SNP_ID_508182209 A-to-I Human chr12 - 79910250 79910250 79910250 GTTTCGAAGTCCTGACCTCAGGTGATCCTCCCACCTCATCCTCCTAAAGTGCTGGGATTACAGGC GTTTCGAAGTCCTGACCTCAGGTGATCCTCCCGCCTCATCCTCCTAAAGTGCTGGGATTACAGGC T C PPP1R12A Ensembl:ENSG00000058272 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1157745275 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15943,RMVar_hsa_circ_45403,RMVar_hsa_circ_35743,RMVar_hsa_circ_80456,RMVar_hsa_circ_158532 5687 RMVar_ID_5687 Human_SNP_ID_508187274 A-to-I Human chr12 - 79930590 79930590 79930590 TTTTGTATTTTTAGTAGAGATGCGGTTTCTCTATGTTGATCAGACTGGTCTCGAACTCCTGACCT TTTTGTATTTTTAGTAGAGATGCGGTTTCTCTTTGTTGATCAGACTGGTCTCGAACTCCTGACCT T A PPP1R12A Ensembl:ENSG00000058272 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs544345435 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12044872,Human_RBP_ID_25006300 RMVar_hsa_circ_15943,RMVar_hsa_circ_45403,RMVar_hsa_circ_35743,RMVar_hsa_circ_80456,RMVar_hsa_circ_158532 5688 RMVar_ID_5688 Human_SNP_ID_508187275 A-to-I Human chr12 - 79930590 79930590 79930590 TTTTGTATTTTTAGTAGAGATGCGGTTTCTCTATGTTGATCAGACTGGTCTCGAACTCCTGACCT TTTTGTATTTTTAGTAGAGATGCGGTTTCTCTGTGTTGATCAGACTGGTCTCGAACTCCTGACCT T C PPP1R12A Ensembl:ENSG00000058272 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs544345435 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12044872,Human_RBP_ID_25006300 RMVar_hsa_circ_15943,RMVar_hsa_circ_45403,RMVar_hsa_circ_35743,RMVar_hsa_circ_80456,RMVar_hsa_circ_158532 5689 RMVar_ID_5689 Human_SNP_ID_508187276 A-to-I Human chr12 - 79930590 79930590 79930590 TTTTGTATTTTTAGTAGAGATGCGGTTTCTCTATGTTGATCAGACTGGTCTCGAACTCCTGACCT TTTTGTATTTTTAGTAGAGATGCGGTTTCTCTCTGTTGATCAGACTGGTCTCGAACTCCTGACCT T G PPP1R12A Ensembl:ENSG00000058272 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs544345435 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12044872,Human_RBP_ID_25006300 RMVar_hsa_circ_15943,RMVar_hsa_circ_45403,RMVar_hsa_circ_35743,RMVar_hsa_circ_80456,RMVar_hsa_circ_158532 5690 RMVar_ID_5690 Human_SNP_ID_513113870 A-to-I Human chr12 - 100009456 100009456 100009456 GAGGCCAAGTACAAGTTGTGCAAAGTGAGAAAAATCTTTGTGGGCACAAAAGGAATCTCTCGTCT GAGGCCAAGTACAAGTTGTGCAAAGTGAGAAAGATCTTTGTGGGCACAAAAGGAATCTCTCGTCT T C RPS4XP1 Ensembl:ENSG00000214203 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878998246 Functional Loss SNV dbSNP153 33..33 33 - - - 5691 RMVar_ID_5691 Human_SNP_ID_513119802 A-to-I Human chr12 - 100033804 100033804 100033804 ACTTGAGGCTGGGCGCGGTGGCTCATCCCTGTAATCTCAGCACTTTGGGAGGCCAAATTGGGCAG ACTTGAGGCTGGGCGCGGTGGCTCATCCCTGTCATCTCAGCACTTTGGGAGGCCAAATTGGGCAG T G UHRF1BP1L,AC126474.2 Ensembl:ENSG00000111647,Ensembl:ENSG00000280088 Protein coding,Other intron,exon GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1444884813 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_3146568,Human_miRNA_ID_3146802,Human_miRNA_ID_3154855,Human_miRNA_ID_3156739,Human_miRNA_ID_3161538,Human_miRNA_ID_3161773,Human_miRNA_ID_3168096,Human_miRNA_ID_3168314,Human_miRNA_ID_3168534,Human_miRNA_ID_3168754,Human_miRNA_ID_3168969,Human_miRNA_ID_3180368,Human_miRNA_ID_3180586,Human_miRNA_ID_3195426,Human_miRNA_ID_3197838,Human_miRNA_ID_3198212,Human_miRNA_ID_3198597,Human_miRNA_ID_3198815,Human_miRNA_ID_3199086,Human_miRNA_ID_3199451,Human_miRNA_ID_3199784,Human_miRNA_ID_3200020,Human_miRNA_ID_3200942,Human_miRNA_ID_3215870 5692 RMVar_ID_5692 Human_SNP_ID_513120227 A-to-I Human chr12 - 100035561 100035561 100035561 CCCCAGGTGATCCGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGTACC CCCCAGGTGATCCGCCCACCTCGGCCTCCCAAGGTGCTGGGATTACAGGCGTGAGCCACCGTACC T C UHRF1BP1L Ensembl:ENSG00000111647 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1218572311 Functional Loss SNV dbSNP153 33..33 33 - - - 5693 RMVar_ID_5693 Human_SNP_ID_513120297 A-to-I Human chr12 - 100035771 100035771 100035771 TGAGGTTTCGCTCTTGTTGCCCAGGCTGGAGTACAATGGTGTGATCTTAGCTCACCGCAACCTCC TGAGGTTTCGCTCTTGTTGCCCAGGCTGGAGTGCAATGGTGTGATCTTAGCTCACCGCAACCTCC T C UHRF1BP1L Ensembl:ENSG00000111647 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs561663267 Functional Loss SNV dbSNP153 33..33 33 - - - 5694 RMVar_ID_5694 Human_SNP_ID_513123205 A-to-I Human chr12 - 100047460 100047460 100047460 AATTTTGCTCTTGTTGCCCAGGCTTGAGTGCAATGGCACGATCTCAGCCTACTGCAAACCTCTGC AATTTTGCTCTTGTTGCCCAGGCTTGAGTGCAGTGGCACGATCTCAGCCTACTGCAAACCTCTGC T C UHRF1BP1L Ensembl:ENSG00000111647 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs907699722 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57646,RMVar_hsa_circ_288377,RMVar_hsa_circ_326254,RMVar_hsa_circ_268072,RMVar_hsa_circ_159118 5695 RMVar_ID_5695 Human_SNP_ID_513129482 A-to-I Human chr12 - 100070884 100070884 100070884 GGTTCAAGTGATTCTCCTGAGTAGCTGGGACTACAGGCATGCACCACCACATCTGGCTGATTTTT GGTTCAAGTGATTCTCCTGAGTAGCTGGGACTTCAGGCATGCACCACCACATCTGGCTGATTTTT T A UHRF1BP1L Ensembl:ENSG00000111647 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1199825604 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57646,RMVar_hsa_circ_288377,RMVar_hsa_circ_288587,RMVar_hsa_circ_311731,RMVar_hsa_circ_159118,RMVar_hsa_circ_49976,RMVar_hsa_circ_127644,RMVar_hsa_circ_159119,RMVar_hsa_circ_159120,RMVar_hsa_circ_265188,RMVar_hsa_circ_85458,RMVar_hsa_circ_159125,RMVar_hsa_circ_57074,RMVar_hsa_circ_159124 5696 RMVar_ID_5696 Human_SNP_ID_513156664 A-to-I Human chr12 - 100175667 100175655 100175668 GGGATTTTCCCGCCTCAGCCTCCCAAGTAGCTAGGACTACAGGTGTGTGCCACCACGCTCTGCTA GGGATTTTCCCGCCTCAGCCTCCCAAGTAGC_____________GTGTGCCACCACGCTCTGCTA CACCTGTAGTCCTA C AC010203.1 Ensembl:ENSG00000257489 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1173833951 Functional Loss DEL dbSNP153 32..44 33 - - - 5697 RMVar_ID_5697 Human_SNP_ID_513164451 A-to-I Human chr12 + 100207936 100207936 100207936 TAACCCCATCAGTTTGGGAGGCTGAGGCGAGTAGATCACTTGAGTTTAGGATTTGAGATCAGCCT TAACCCCATCAGTTTGGGAGGCTGAGGCGAGTGGATCACTTGAGTTTAGGATTTGAGATCAGCCT A G ACTR6 Ensembl:ENSG00000075089 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277126122 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34622,RMVar_hsa_circ_16715,RMVar_hsa_circ_318171,RMVar_hsa_circ_159151,RMVar_hsa_circ_311920,RMVar_hsa_circ_65023,RMVar_hsa_circ_338762,RMVar_hsa_circ_291315,RMVar_hsa_circ_159152,RMVar_hsa_circ_159153 5698 RMVar_ID_5698 Human_SNP_ID_513164484 A-to-I Human chr12 + 100208040 100208040 100208040 AAAATTAGTTGGGCATGGTGACACGCACCTGTAGTCCCAGCTACTTAGGAAGCTGAGGCAGAAGG AAAATTAGTTGGGCATGGTGACACGCACCTGTCGTCCCAGCTACTTAGGAAGCTGAGGCAGAAGG A C ACTR6 Ensembl:ENSG00000075089 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs574587936 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34622,RMVar_hsa_circ_16715,RMVar_hsa_circ_318171,RMVar_hsa_circ_159151,RMVar_hsa_circ_311920,RMVar_hsa_circ_65023,RMVar_hsa_circ_338762,RMVar_hsa_circ_291315,RMVar_hsa_circ_159152,RMVar_hsa_circ_159153 5699 RMVar_ID_5699 Human_SNP_ID_513164676 A-to-I Human chr12 + 100208917 100208917 100208917 CACAGGTATGTGCTGCCACATCTGGCTGATTTATTTATTTTTTGTAGAGACAGGGTCTCATTTTG CACAGGTATGTGCTGCCACATCTGGCTGATTTGTTTATTTTTTGTAGAGACAGGGTCTCATTTTG A G ACTR6 Ensembl:ENSG00000075089 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1414131912 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34622,RMVar_hsa_circ_16715,RMVar_hsa_circ_318171,RMVar_hsa_circ_159151,RMVar_hsa_circ_311920,RMVar_hsa_circ_65023,RMVar_hsa_circ_338762,RMVar_hsa_circ_291315,RMVar_hsa_circ_159152,RMVar_hsa_circ_159153 5700 RMVar_ID_5700 Human_SNP_ID_513176557 A-to-I Human chr12 - 100260259 100260259 100260259 AAGATTAGCCAGGTGTCGTGGTGCGTGCCTATAATCCTAGCTACTCTGGAGGCTGAGGCATGAGA AAGATTAGCCAGGTGTCGTGGTGCGTGCCTATGATCCTAGCTACTCTGGAGGCTGAGGCATGAGA T C DEPDC4 Ensembl:ENSG00000166153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1205380310 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_159160,RMVar_hsa_circ_98564,RMVar_hsa_circ_159159,RMVar_hsa_circ_309183,RMVar_hsa_circ_62205 5701 RMVar_ID_5701 Human_SNP_ID_513176682 A-to-I Human chr12 - 100260810 100260810 100260810 CTCACTGTAAACTCTGCCTCCCAGGTTCAAGCAAGTCTTGTGCCTCAGCCTCCAGAGTAGTTGGA CTCACTGTAAACTCTGCCTCCCAGGTTCAAGCGAGTCTTGTGCCTCAGCCTCCAGAGTAGTTGGA T C DEPDC4 Ensembl:ENSG00000166153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1380109953 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_159160,RMVar_hsa_circ_98564,RMVar_hsa_circ_159159,RMVar_hsa_circ_309183,RMVar_hsa_circ_62205 5702 RMVar_ID_5702 Human_SNP_ID_513181792 A-to-I Human chr12 + 100281212 100281212 100281212 TGCCATTCCTGGCTAATTTTCGAATTTTTTGTAGGGACAGGGTTTCTCCATGTTTCCCAGGCTGG TGCCATTCCTGGCTAATTTTCGAATTTTTTGTGGGGACAGGGTTTCTCCATGTTTCCCAGGCTGG A G SCYL2 Ensembl:ENSG00000136021 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs534887843 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_159161 5703 RMVar_ID_5703 Human_SNP_ID_513182277 A-to-I Human chr12 + 100282941 100282941 100282941 TGATCAGTTCTCCACTATCCTTCTGTTTTTCTAGGTAACTATAACTACCCAATATTGCAGCCATG TGATCAGTTCTCCACTATCCTTCTGTTTTTCTCGGTAACTATAACTACCCAATATTGCAGCCATG A C SCYL2 Ensembl:ENSG00000136021 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1013375499 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_874959,Human_RBP_ID_4248233,Human_RBP_ID_25017591 RMVar_hsa_circ_58554,RMVar_hsa_circ_317137,RMVar_hsa_circ_360986,RMVar_hsa_circ_159161,RMVar_hsa_circ_368950,RMVar_hsa_circ_373859,RMVar_hsa_circ_350332,RMVar_hsa_circ_352434,RMVar_hsa_circ_325940,RMVar_hsa_circ_270654,RMVar_hsa_circ_309200,RMVar_hsa_circ_269868 5704 RMVar_ID_5704 Human_SNP_ID_513262915 A-to-I Human chr12 + 100627460 100627460 100627460 CCAGGCCCAGCTAATTTTTTTGTATTTTCAGTAGAGATGGGGGTTTCACCATGTCGGCCAGGCTG CCAGGCCCAGCTAATTTTTTTGTATTTTCAGTGGAGATGGGGGTTTCACCATGTCGGCCAGGCTG A G GAS2L3 Ensembl:ENSG00000139354 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490829,GSM3490830,GSM3490831 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,EC109 cell line - 29129909,31158229,31158229,32596459 RNA-Seq:(High) rs1158163530 Functional Loss SNV dbSNP153 33..33 33 - - - 5705 RMVar_ID_5705 Human_SNP_ID_513262918 A-to-I Human chr12 + 100627475 100627475 100627475 TTTTTTGTATTTTCAGTAGAGATGGGGGTTTCACCATGTCGGCCAGGCTGATCTCAAACTCCTGA TTTTTTGTATTTTCAGTAGAGATGGGGGTTTCGCCATGTCGGCCAGGCTGATCTCAAACTCCTGA A G GAS2L3 Ensembl:ENSG00000139354 Protein coding 3'UTR GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs1056670009 Functional Loss SNV dbSNP153 33..33 33 - - - 5706 RMVar_ID_5706 Human_SNP_ID_513428461 A-to-I Human chr12 + 101314936 101314935 101314936 CAGCCTAGTGAAATCCCGTCTCTACTAAAAATACAAAAATTAGCTGGGCATGGTGGTGCCTGCCT CAGCCTAGTGAAATCCCGTCTCTACTAAAAAT_CAAAAATTAGCTGGGCATGGTGGTGCCTGCCT TA T UTP20 Ensembl:ENSG00000120800 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946140780 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_9132,RMVar_hsa_circ_28847,RMVar_hsa_circ_67587,RMVar_hsa_circ_110546,RMVar_hsa_circ_159239,RMVar_hsa_circ_95319,RMVar_hsa_circ_65437,RMVar_hsa_circ_159244,RMVar_hsa_circ_265543,RMVar_hsa_circ_328370,RMVar_hsa_circ_127748,RMVar_hsa_circ_159246,RMVar_hsa_circ_359234,RMVar_hsa_circ_316048,RMVar_hsa_circ_87729,RMVar_hsa_circ_106587,RMVar_hsa_circ_159247,RMVar_hsa_circ_89728,RMVar_hsa_circ_80368,RMVar_hsa_circ_159251,RMVar_hsa_circ_159252,RMVar_hsa_circ_159250,RMVar_hsa_circ_363803,RMVar_hsa_circ_159254,RMVar_hsa_circ_159255 5707 RMVar_ID_5707 Human_SNP_ID_513428466 A-to-I Human chr12 + 101314945 101314945 101314945 GAAATCCCGTCTCTACTAAAAATACAAAAATTAGCTGGGCATGGTGGTGCCTGCCTGTAAGTCCC GAAATCCCGTCTCTACTAAAAATACAAAAATTGGCTGGGCATGGTGGTGCCTGCCTGTAAGTCCC A G UTP20 Ensembl:ENSG00000120800 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1451268746 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9132,RMVar_hsa_circ_28847,RMVar_hsa_circ_67587,RMVar_hsa_circ_110546,RMVar_hsa_circ_159239,RMVar_hsa_circ_95319,RMVar_hsa_circ_65437,RMVar_hsa_circ_159244,RMVar_hsa_circ_265543,RMVar_hsa_circ_328370,RMVar_hsa_circ_127748,RMVar_hsa_circ_159246,RMVar_hsa_circ_359234,RMVar_hsa_circ_316048,RMVar_hsa_circ_87729,RMVar_hsa_circ_106587,RMVar_hsa_circ_159247,RMVar_hsa_circ_89728,RMVar_hsa_circ_80368,RMVar_hsa_circ_159251,RMVar_hsa_circ_159252,RMVar_hsa_circ_159250,RMVar_hsa_circ_363803,RMVar_hsa_circ_159254,RMVar_hsa_circ_159255 5708 RMVar_ID_5708 Human_SNP_ID_513443948 A-to-I Human chr12 - 101379880 101379880 101379880 GGGAGGCAGAGGTTGCAGTGACCCGAGATCACACCACTGCACGCCAGCCTGGGTGACAGAGTGAG GGGAGGCAGAGGTTGCAGTGACCCGAGATCACGCCACTGCACGCCAGCCTGGGTGACAGAGTGAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1339619159 Functional Loss SNV dbSNP153 33..33 33 - - - 5709 RMVar_ID_5709 Human_SNP_ID_513445054 A-to-I Human chr12 - 101383990 101383990 101383990 CTTTTTAAAAATAAACTCTGGCTGGGTACAGTAGCTCACTTCTATAGTCTCAACACTTTGGGAGG CTTTTTAAAAATAAACTCTGGCTGGGTACAGTGGCTCACTTCTATAGTCTCAACACTTTGGGAGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215491827 Functional Loss SNV dbSNP153 33..33 33 - - - 5710 RMVar_ID_5710 Human_SNP_ID_513448527 A-to-I Human chr12 - 101397664 101397664 101397664 GAAACCTCATCTCTACTAAAAATACAAAAATTAGCTGGGCGTGGCAGCGGGCACCTGTAGTCCCA GAAACCTCATCTCTACTAAAAATACAAAAATTGGCTGGGCGTGGCAGCGGGCACCTGTAGTCCCA T C ARL1 Ensembl:ENSG00000120805 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1229567310 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_355113,RMVar_hsa_circ_364857,RMVar_hsa_circ_296853,RMVar_hsa_circ_159282 5711 RMVar_ID_5711 Human_SNP_ID_513448894 A-to-I Human chr12 - 101399249 101399249 101399249 CTCCTGATCTGCCAGCCTTGGCCTCCCAAAGTACTGGGATTACAGGCATGAGCCACCGCGCTCAG CTCCTGATCTGCCAGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCGCTCAG T C ARL1 Ensembl:ENSG00000120805 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1250432845 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_355113,RMVar_hsa_circ_364857,RMVar_hsa_circ_296853,RMVar_hsa_circ_159282 5712 RMVar_ID_5712 Human_SNP_ID_513448923 A-to-I Human chr12 - 101399355 101399355 101399355 GGCTTCTGCCACCACACCCGGCTTATTTTTGTATTTGTAGCAGAGATGGGGTTTCACCATGTTGG GGCTTCTGCCACCACACCCGGCTTATTTTTGTGTTTGTAGCAGAGATGGGGTTTCACCATGTTGG T C ARL1 Ensembl:ENSG00000120805 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1326342717 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_355113,RMVar_hsa_circ_364857,RMVar_hsa_circ_296853,RMVar_hsa_circ_159282 5713 RMVar_ID_5713 Human_SNP_ID_513450161 A-to-I Human chr12 - 101404308 101404308 101404308 CATAGCTCACTGCAGCGTCTACCTCTACCTCTACCTCCTGGGCTCAAGCGATCTTCCCACCTCAG CATAGCTCACTGCAGCGTCTACCTCTACCTCTGCCTCCTGGGCTCAAGCGATCTTCCCACCTCAG T C ARL1 Ensembl:ENSG00000120805 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1468012396 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12318,RMVar_hsa_circ_296853,RMVar_hsa_circ_159282 5714 RMVar_ID_5714 Human_SNP_ID_513536356 A-to-I Human chr12 + 101745879 101745879 101745879 AATATGGTGGAACCCCCGTCTCTACTAAAAATACAAAAATTAGCAGGGTGTGGTGGCATGCACCT AATATGGTGGAACCCCCGTCTCTACTAAAAATGCAAAAATTAGCAGGGTGTGGTGGCATGCACCT A G NONHSAG012082.2 RNACentral:URS00009B616C lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1194632811 Functional Loss SNV dbSNP153 33..33 33 - - - 5715 RMVar_ID_5715 Human_SNP_ID_513539209 A-to-I Human chr12 - 101758112 101758112 101758112 ATCACTTGAACCCGAGAGGTGGAAGTTGCAGTAAGCTGAGATCGCGCCACTGCACTCCAGCCTGG ATCACTTGAACCCGAGAGGTGGAAGTTGCAGTTAGCTGAGATCGCGCCACTGCACTCCAGCCTGG T A GNPTAB Ensembl:ENSG00000111670 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs545894539 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2308,RMVar_hsa_circ_10438,RMVar_hsa_circ_33888,RMVar_hsa_circ_301460,RMVar_hsa_circ_159288,RMVar_hsa_circ_274970,RMVar_hsa_circ_57027,RMVar_hsa_circ_159290,RMVar_hsa_circ_4897,RMVar_hsa_circ_329739,RMVar_hsa_circ_159289,RMVar_hsa_circ_306157,RMVar_hsa_circ_159291,RMVar_hsa_circ_159292 5716 RMVar_ID_5716 Human_SNP_ID_513545229 A-to-I Human chr12 - 101781603 101781603 101781603 CATGGCTCACCACAGCCCCAACTCCGGGGCTCAGATGATCCTCCCATCTCAGCCTCCTGAGTAGC CATGGCTCACCACAGCCCCAACTCCGGGGCTCCGATGATCCTCCCATCTCAGCCTCCTGAGTAGC T G GNPTAB Ensembl:ENSG00000111670 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1428329755 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4897,RMVar_hsa_circ_26322,RMVar_hsa_circ_27259,RMVar_hsa_circ_267094,RMVar_hsa_circ_303731,RMVar_hsa_circ_159296,RMVar_hsa_circ_10182,RMVar_hsa_circ_159295,RMVar_hsa_circ_159297,RMVar_hsa_circ_370865,RMVar_hsa_circ_373813,RMVar_hsa_circ_159298,RMVar_hsa_circ_39284,RMVar_hsa_circ_159303,RMVar_hsa_circ_95699,RMVar_hsa_circ_159300,RMVar_hsa_circ_304408,RMVar_hsa_circ_315571,RMVar_hsa_circ_303309,RMVar_hsa_circ_159305,RMVar_hsa_circ_274160,RMVar_hsa_circ_159304,RMVar_hsa_circ_159302,RMVar_hsa_circ_268117 5717 RMVar_ID_5717 Human_SNP_ID_513548236 A-to-I Human chr12 - 101794397 101794397 101794397 CGATCCTCTTACCTCAGCCTCCCAAAGTGTTAAGATTACAGGTGTGAGCCACCATACCTGGCCAG CGATCCTCTTACCTCAGCCTCCCAAAGTGTTAGGATTACAGGTGTGAGCCACCATACCTGGCCAG T C GNPTAB Ensembl:ENSG00000111670 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1039432731 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39284,RMVar_hsa_circ_35905,RMVar_hsa_circ_159305,RMVar_hsa_circ_274160,RMVar_hsa_circ_272003,RMVar_hsa_circ_159307,RMVar_hsa_circ_345782 5718 RMVar_ID_5718 Human_SNP_ID_513553112 A-to-I Human chr12 - 101814133 101814133 101814133 CACCATACCTGGCTAATTTTTGTAGTTTTTGTAGAGATGGTGTTTCATCATGTTGCCCAGCTGGT CACCATACCTGGCTAATTTTTGTAGTTTTTGTGGAGATGGTGTTTCATCATGTTGCCCAGCTGGT T C GNPTAB Ensembl:ENSG00000111670 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1036893992 Functional Loss SNV dbSNP153 33..33 33 - - - 5719 RMVar_ID_5719 Human_SNP_ID_513553113 A-to-I Human chr12 - 101814133 101814133 101814133 CACCATACCTGGCTAATTTTTGTAGTTTTTGTAGAGATGGTGTTTCATCATGTTGCCCAGCTGGT CACCATACCTGGCTAATTTTTGTAGTTTTTGTCGAGATGGTGTTTCATCATGTTGCCCAGCTGGT T G GNPTAB Ensembl:ENSG00000111670 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1036893992 Functional Loss SNV dbSNP153 33..33 33 - - - 5720 RMVar_ID_5720 Human_SNP_ID_513569906 A-to-I Human chr12 + 101880469 101880469 101880469 CCACCACGCCCAGCTAATATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGC CCACCACGCCCAGCTAATATTTTTGTATTTTTGGTAGAGACGGGGTTTCACCATGTTGGCCAGGC A G DRAM1 Ensembl:ENSG00000136048 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1024791592 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91341,RMVar_hsa_circ_101936,RMVar_hsa_circ_159311,RMVar_hsa_circ_159312 5721 RMVar_ID_5721 Human_SNP_ID_513571888 A-to-I Human chr12 + 101888365 101888365 101888365 GTTGGTTAGGCTGGTCTCGAACTCTTGACCTCAGGCGATCCACCCACCTCAGCCTCCCGAAGTGC GTTGGTTAGGCTGGTCTCGAACTCTTGACCTCGGGCGATCCACCCACCTCAGCCTCCCGAAGTGC A G DRAM1 Ensembl:ENSG00000136048 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1239245585 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91341,RMVar_hsa_circ_101936,RMVar_hsa_circ_159311,RMVar_hsa_circ_159312 5722 RMVar_ID_5722 Human_SNP_ID_513576522 A-to-I Human chr12 + 101905805 101905805 101905805 ATTTATTTATTTATGTATTTATTTATTTTTTGAGATGGAGTCTCGCTCTGTCTCCCAGACTGTAT ATTTATTTATTTATGTATTTATTTATTTTTTGCGATGGAGTCTCGCTCTGTCTCCCAGACTGTAT A C DRAM1 Ensembl:ENSG00000136048 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs771223968 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91341,RMVar_hsa_circ_159314,RMVar_hsa_circ_159312,RMVar_hsa_circ_361742,RMVar_hsa_circ_310622,RMVar_hsa_circ_159315,RMVar_hsa_circ_89797,RMVar_hsa_circ_346945,RMVar_hsa_circ_159317,RMVar_hsa_circ_159318 5723 RMVar_ID_5723 Human_SNP_ID_513577945 A-to-I Human chr12 + 101911007 101911007 101911007 CCTGTAATCCCAGCACGTTGGGAGGCCGAGGCAGGTGGATCACTTGAGGTCAGGAGTTCGGGACC CCTGTAATCCCAGCACGTTGGGAGGCCGAGGCGGGTGGATCACTTGAGGTCAGGAGTTCGGGACC A G DRAM1 Ensembl:ENSG00000136048 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs965495894 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91341,RMVar_hsa_circ_159314,RMVar_hsa_circ_159312,RMVar_hsa_circ_361742,RMVar_hsa_circ_310622,RMVar_hsa_circ_159315,RMVar_hsa_circ_89797,RMVar_hsa_circ_346945,RMVar_hsa_circ_159317,RMVar_hsa_circ_159318,RMVar_hsa_circ_286751,RMVar_hsa_circ_304156,RMVar_hsa_circ_159319 5724 RMVar_ID_5724 Human_SNP_ID_513578179 A-to-I Human chr12 + 101912078 101912078 101912078 AAAACTAGCCAGGTGTGGTGGTGGGCACCTGTAATCCCAGCTGCTGAGGAGGCTGAGGCAGGAGA AAAACTAGCCAGGTGTGGTGGTGGGCACCTGTCATCCCAGCTGCTGAGGAGGCTGAGGCAGGAGA A C DRAM1 Ensembl:ENSG00000136048 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1366879883 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91341,RMVar_hsa_circ_159314,RMVar_hsa_circ_159312,RMVar_hsa_circ_361742,RMVar_hsa_circ_310622,RMVar_hsa_circ_159315,RMVar_hsa_circ_89797,RMVar_hsa_circ_346945,RMVar_hsa_circ_159317,RMVar_hsa_circ_159318,RMVar_hsa_circ_286751,RMVar_hsa_circ_304156,RMVar_hsa_circ_159319 5725 RMVar_ID_5725 Human_SNP_ID_513579237 A-to-I Human chr12 + 101916235 101916235 101916235 AGATATCGAGGTTAGAAACATGGGCCTAGGCCAGGTGCTGTGGTTCATGCCTGTAATCCCAGCAC AGATATCGAGGTTAGAAACATGGGCCTAGGCCCGGTGCTGTGGTTCATGCCTGTAATCCCAGCAC A C DRAM1 Ensembl:ENSG00000136048 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs977815260 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_361742,RMVar_hsa_circ_159315,RMVar_hsa_circ_89797,RMVar_hsa_circ_159318,RMVar_hsa_circ_286751 5726 RMVar_ID_5726 Human_SNP_ID_513630315 A-to-I Human chr12 + 102136978 102136977 102136979 GTTTTTTTTGTTTGTTTGTTTGTTTTTGAGACAGAGTCTCACTCTGTCACCCAGGCTGGAGTGCA GTTTTTTTTGTTTGTTTGTTTGTTTTTGAGAC__AGTCTCACTCTGTCACCCAGGCTGGAGTGCA CAG C PARPBP Ensembl:ENSG00000185480 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1424567846 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_65937,RMVar_hsa_circ_371761,RMVar_hsa_circ_159332,RMVar_hsa_circ_159333 5727 RMVar_ID_5727 Human_SNP_ID_514029291 A-to-I Human chr12 - 103774934 103774934 103774934 TGATCTCGGCTCACTGCAACCTCTTGCCTCCCAGGTTCAAGCAATTTTCGTGCCTCAGCCTCCCG TGATCTCGGCTCACTGCAACCTCTTGCCTCCCGGGTTCAAGCAATTTTCGTGCCTCAGCCTCCCG T C NT5DC3 Ensembl:ENSG00000111696 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1168360196 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116970,RMVar_hsa_circ_159344 5728 RMVar_ID_5728 Human_SNP_ID_514060069 A-to-I Human chr12 - 103906979 103906979 103906979 CTCACTGCAACCTCCATCTCCCGATTCAAGCAATTCTCCTGCCTCTGCCTCCCAAGTAGCTGGGA CTCACTGCAACCTCCATCTCCCGATTCAAGCAGTTCTCCTGCCTCTGCCTCCCAAGTAGCTGGGA T C TTC41P Ensembl:ENSG00000214198 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs544577993 Functional Loss SNV dbSNP153 33..33 33 - - - 5729 RMVar_ID_5729 Human_SNP_ID_514075099 A-to-I Human chr12 + 103967725 103967725 103967725 GTGATCCACCTGCCTCGGCCTCCCAAAGTGCTAGGATTACAAATGTGAGCCACCGGGCCCAGCCG GTGATCCACCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAAATGTGAGCCACCGGGCCCAGCCG A G TDG Ensembl:ENSG00000139372 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1273850826 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123406,RMVar_hsa_circ_159365 5730 RMVar_ID_5730 Human_SNP_ID_514075246 A-to-I Human chr12 + 103968101 103968101 103968101 ATCACTTTGGCCTCCCAAAGTGCTGGGATTACAAGCATGAGCCAAAGCGCCCAGCCTAGACTTTA ATCACTTTGGCCTCCCAAAGTGCTGGGATTACCAGCATGAGCCAAAGCGCCCAGCCTAGACTTTA A C TDG Ensembl:ENSG00000139372 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs952080667 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123406,RMVar_hsa_circ_159365 5731 RMVar_ID_5731 Human_SNP_ID_514075725 A-to-I Human chr12 + 103970371 103970371 103970371 ATAGATGCATGTACCTGTAGTCCCAGCTGCTCAGGAGACTGAGGTGAGAGGATTGTCTGAGCCCA ATAGATGCATGTACCTGTAGTCCCAGCTGCTCGGGAGACTGAGGTGAGAGGATTGTCTGAGCCCA A G TDG Ensembl:ENSG00000139372 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1356100989 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6122529,Human_RBP_ID_11785986 RMVar_hsa_circ_123406,RMVar_hsa_circ_159365 5732 RMVar_ID_5732 Human_SNP_ID_514098343 A-to-I Human chr12 - 104057338 104057338 104057338 TTTTTTATTTTTTGTAGAGACGGGGTCTCCCTATGTTGCTCAGGCTGGTCTTGAACTCCTGAGCT TTTTTTATTTTTTGTAGAGACGGGGTCTCCCTTTGTTGCTCAGGCTGGTCTTGAACTCCTGAGCT T A GLT8D2 Ensembl:ENSG00000120820 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs537348412 Functional Loss SNV dbSNP153 33..33 33 - - - 5733 RMVar_ID_5733 Human_SNP_ID_514098344 A-to-I Human chr12 - 104057338 104057338 104057338 TTTTTTATTTTTTGTAGAGACGGGGTCTCCCTATGTTGCTCAGGCTGGTCTTGAACTCCTGAGCT TTTTTTATTTTTTGTAGAGACGGGGTCTCCCTGTGTTGCTCAGGCTGGTCTTGAACTCCTGAGCT T C GLT8D2 Ensembl:ENSG00000120820 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs537348412 Functional Loss SNV dbSNP153 33..33 33 - - - 5734 RMVar_ID_5734 Human_SNP_ID_514137625 A-to-I Human chr12 + 104229247 104229247 104229247 TTGGCTCATTGCAACTTCTACCTCCTGGGCTCAAGCAATCCTCCCACCTCAGCCTCCTCAGTAGC TTGGCTCATTGCAACTTCTACCTCCTGGGCTCGAGCAATCCTCCCACCTCAGCCTCCTCAGTAGC A G TXNRD1 Ensembl:ENSG00000198431 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs930635101 Functional Loss SNV dbSNP153 33..33 33 - - - 5735 RMVar_ID_5735 Human_SNP_ID_514148632 A-to-I Human chr12 - 104271310 104271310 104271310 TTAGTGGCGGGCACCTGTAGTCCCAGAAACTCAGGAGGCTGAGGCAGGAGAATGGCATGAACCTG TTAGTGGCGGGCACCTGTAGTCCCAGAAACTCGGGAGGCTGAGGCAGGAGAATGGCATGAACCTG T C AC089983.1 Ensembl:ENSG00000257732 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs952425753 Functional Loss SNV dbSNP153 33..33 33 - - - 5736 RMVar_ID_5736 Human_SNP_ID_514148633 A-to-I Human chr12 - 104271310 104271310 104271310 TTAGTGGCGGGCACCTGTAGTCCCAGAAACTCAGGAGGCTGAGGCAGGAGAATGGCATGAACCTG TTAGTGGCGGGCACCTGTAGTCCCAGAAACTCCGGAGGCTGAGGCAGGAGAATGGCATGAACCTG T G AC089983.1 Ensembl:ENSG00000257732 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs952425753 Functional Loss SNV dbSNP153 33..33 33 - - - 5737 RMVar_ID_5737 Human_SNP_ID_514149176 A-to-I Human chr12 + 104273394 104273394 104273394 AGGTGGGTGGATCACAAGGTCAGGAGTTCGAGACCAGCCTGGCCAACGTAGTGAAACCCCGTCTG AGGTGGGTGGATCACAAGGTCAGGAGTTCGAGGCCAGCCTGGCCAACGTAGTGAAACCCCGTCTG A G TXNRD1 Ensembl:ENSG00000198431 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251072333 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59710 5738 RMVar_ID_5738 Human_SNP_ID_514153624 A-to-I Human chr12 + 104291401 104291401 104291401 TTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGTCAGGCTGGTCTCGAACTCCTGACCT TTTTGTATTTTTAGTAGAGATGGGGTTTCACCGTGTTGGTCAGGCTGGTCTCGAACTCCTGACCT A G TXNRD1 Ensembl:ENSG00000198431 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041240146 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 5739 RMVar_ID_5739 Human_SNP_ID_514153732 A-to-I Human chr12 + 104291729 104291729 104291729 TGGTCTTGAACTTTTGACGCCGTGATCCACCCACTTCGGCCTTCCAAAGTGCTGGGATTATGGGC TGGTCTTGAACTTTTGACGCCGTGATCCACCCCCTTCGGCCTTCCAAAGTGCTGGGATTATGGGC A C TXNRD1 Ensembl:ENSG00000198431 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1172375708 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 5740 RMVar_ID_5740 Human_SNP_ID_514153805 A-to-I Human chr12 - 104292084 104292084 104292084 GGGAAAAGGGGATGAGGAAGAAACAATATTAAAAGGAGAAAGGAAAAGTGGACATTTTGAAGAGC GGGAAAAGGGGATGAGGAAGAAACAATATTAAGAGGAGAAAGGAAAAGTGGACATTTTGAAGAGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs567021920 Functional Loss SNV dbSNP153 33..33 33 - - - 5741 RMVar_ID_5741 Human_SNP_ID_514155196 A-to-I Human chr12 + 104297521 104297521 104297521 CCGAGTAGCTGGGATTGCAGGCATGCGCCACCACGTCTGGCTAATTTTGTATTTTTAGTAGAGAC CCGAGTAGCTGGGATTGCAGGCATGCGCCACCGCGTCTGGCTAATTTTGTATTTTTAGTAGAGAC A G TXNRD1 Ensembl:ENSG00000198431 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs770299288 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 5742 RMVar_ID_5742 Human_SNP_ID_514155226 A-to-I Human chr12 + 104297617 104297617 104297617 GAACTCCTGACCTCAGGTGATCCGCCTGCGTCAGCCTCCAAAAGTGCTGAGATTACAGGTGTAAG GAACTCCTGACCTCAGGTGATCCGCCTGCGTCGGCCTCCAAAAGTGCTGAGATTACAGGTGTAAG A G TXNRD1 Ensembl:ENSG00000198431 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1288428198 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 5743 RMVar_ID_5743 Human_SNP_ID_514160668 A-to-I Human chr12 + 104317978 104317978 104317978 CCTGGCCAACATGGCAAAACTGCGTCTCTACTAAAAATATAAACAATTAGCTGGGCATGATGGCC CCTGGCCAACATGGCAAAACTGCGTCTCTACTGAAAATATAAACAATTAGCTGGGCATGATGGCC A G TXNRD1 Ensembl:ENSG00000198431 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031254815 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_361855,RMVar_hsa_circ_285014,RMVar_hsa_circ_56236,RMVar_hsa_circ_62185,RMVar_hsa_circ_159396,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_12512,RMVar_hsa_circ_159397,RMVar_hsa_circ_159398,RMVar_hsa_circ_47757,RMVar_hsa_circ_76150,RMVar_hsa_circ_353210,RMVar_hsa_circ_159402 5744 RMVar_ID_5744 Human_SNP_ID_514161525 A-to-I Human chr12 - 104321340 104321340 104321340 TTTTTGCCTTTTACTGTGAATGTAGAATCAAGAAACCTACAGGCAAACCCACTTACTTTAATTGG TTTTTGCCTTTTACTGTGAATGTAGAATCAAGGAACCTACAGGCAAACCCACTTACTTTAATTGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1214961686 Functional Loss SNV dbSNP153 33..33 33 - - - 5745 RMVar_ID_5745 Human_SNP_ID_514166116 A-to-I Human chr12 + 104338433 104338433 104338433 CTCTGGCCATTTTTCCAGGTGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGT CTCTGGCCATTTTTCCAGGTGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGT A G TXNRD1 Ensembl:ENSG00000198431 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1291578895 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_285014,RMVar_hsa_circ_286706,RMVar_hsa_circ_159397,RMVar_hsa_circ_352554,RMVar_hsa_circ_275981,RMVar_hsa_circ_159406,RMVar_hsa_circ_159407,RMVar_hsa_circ_80885,RMVar_hsa_circ_325144 5746 RMVar_ID_5746 Human_SNP_ID_514167917 A-to-I Human chr12 + 104346082 104346082 104346082 TCACCCAGGCTGGAGTGCAGTGGTGTGATCTCAGTTCACTGCAGCCTTGACCTTTCAAGCTCAAG TCACCCAGGCTGGAGTGCAGTGGTGTGATCTCGGTTCACTGCAGCCTTGACCTTTCAAGCTCAAG A G TXNRD1 Ensembl:ENSG00000198431 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1190327304 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1417184,Human_Splice_Rec_1417185 RMVar_hsa_circ_159407,RMVar_hsa_circ_80885 5747 RMVar_ID_5747 Human_SNP_ID_514168081 A-to-I Human chr12 + 104346839 104346839 104346839 ACTATTGGCCAGGCACAGTGGCTCATGCCTGTAATCTAAGCACTTTGGGAGGCCGAGGCAGGTGG ACTATTGGCCAGGCACAGTGGCTCATGCCTGTCATCTAAGCACTTTGGGAGGCCGAGGCAGGTGG A C TXNRD1 Ensembl:ENSG00000198431 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1464494962 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11788224 RMVar_hsa_circ_159407,RMVar_hsa_circ_80885 5748 RMVar_ID_5748 Human_SNP_ID_514168110 A-to-I Human chr12 + 104346974 104346974 104346974 AAAATTATCCGAGCATGGTGGCAGGTGCCTGTAATCCCACCTACTCGGGAGGCTGAGGCAGGAGA AAAATTATCCGAGCATGGTGGCAGGTGCCTGTGATCCCACCTACTCGGGAGGCTGAGGCAGGAGA A G TXNRD1 Ensembl:ENSG00000198431 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1209439139 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_159407,RMVar_hsa_circ_80885 5749 RMVar_ID_5749 Human_SNP_ID_514184400 A-to-I Human chr12 + 104414412 104414412 104414412 ACCTGTGTGTGTTTGTGCTGTGAATTAAATATATATGTCCCCGTAAAATTCCTGTGTTGAAGCCT ACCTGTGTGTGTTTGTGCTGTGAATTAAATATTTATGTCCCCGTAAAATTCCTGTGTTGAAGCCT A T lnc-TXNRD1-3 RNACentral:URS00009BE262 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1174101308 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3390750 5750 RMVar_ID_5750 Human_SNP_ID_514190229 A-to-I Human chr12 + 104439467 104439467 104439467 GCCCCAGTCTCTCCTTCTGCCTTCTGCCCCTTAGTCGAATTCTTTCTTCTGAGGAGGCAAAAATT GCCCCAGTCTCTCCTTCTGCCTTCTGCCCCTTCGTCGAATTCTTTCTTCTGAGGAGGCAAAAATT A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991402986 Functional Loss SNV dbSNP153 33..33 33 - - - 5751 RMVar_ID_5751 Human_SNP_ID_514190230 A-to-I Human chr12 + 104439467 104439467 104439467 GCCCCAGTCTCTCCTTCTGCCTTCTGCCCCTTAGTCGAATTCTTTCTTCTGAGGAGGCAAAAATT GCCCCAGTCTCTCCTTCTGCCTTCTGCCCCTTTGTCGAATTCTTTCTTCTGAGGAGGCAAAAATT A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991402986 Functional Loss SNV dbSNP153 33..33 33 - - - 5752 RMVar_ID_5752 Human_SNP_ID_514319343 A-to-I Human chr12 + 104995949 104995947 104995949 TGACCTCGTGTTCCACCCTTCTTGACCTGCCAAAGTGTTGGGATTACAGGCATGAGCCACCGTGC TGACCTCGTGTTCCACCCTTCTTGACCTGCC__AGTGTTGGGATTACAGGCATGAGCCACCGTGC CAA C C12orf45 Ensembl:ENSG00000151131 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1183685508 Functional Loss DEL dbSNP153 32..33 33 - - - Human_Splice_Rec_1417303,Human_Splice_Rec_1417311,Human_Splice_Rec_1417319,Human_Splice_Rec_1417327 RMVar_hsa_circ_272804,RMVar_hsa_circ_364855,RMVar_hsa_circ_159444,RMVar_hsa_circ_364982 5753 RMVar_ID_5753 Human_SNP_ID_514319344 A-to-I Human chr12 + 104995949 104995949 104995949 TGACCTCGTGTTCCACCCTTCTTGACCTGCCAAAGTGTTGGGATTACAGGCATGAGCCACCGTGC TGACCTCGTGTTCCACCCTTCTTGACCTGCCACAGTGTTGGGATTACAGGCATGAGCCACCGTGC A C C12orf45 Ensembl:ENSG00000151131 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1456821470 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1417303,Human_Splice_Rec_1417311,Human_Splice_Rec_1417319,Human_Splice_Rec_1417327 RMVar_hsa_circ_272804,RMVar_hsa_circ_364855,RMVar_hsa_circ_159444,RMVar_hsa_circ_364982 5754 RMVar_ID_5754 Human_SNP_ID_514350895 A-to-I Human chr12 + 105124418 105124418 105124418 TCATGTTTTTGTGCTGGTTGGGAACTGAACCTATGGTTTCTGTGAGGTGTGCCTGTATTGTGTTT TCATGTTTTTGTGCTGGTTGGGAACTGAACCTGTGGTTTCTGTGAGGTGTGCCTGTATTGTGTTT A G WASHC4 Ensembl:ENSG00000136051 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1196830 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_216,RMVar_hsa_circ_37136,RMVar_hsa_circ_354817,RMVar_hsa_circ_318565,RMVar_hsa_circ_61137,RMVar_hsa_circ_80717,RMVar_hsa_circ_34198,RMVar_hsa_circ_33146,RMVar_hsa_circ_35120,RMVar_hsa_circ_159456,RMVar_hsa_circ_159457,RMVar_hsa_circ_159458,RMVar_hsa_circ_303507,RMVar_hsa_circ_43972,RMVar_hsa_circ_70770,RMVar_hsa_circ_21778,RMVar_hsa_circ_24261,RMVar_hsa_circ_159460,RMVar_hsa_circ_33128,RMVar_hsa_circ_42554,RMVar_hsa_circ_2601,RMVar_hsa_circ_34317,RMVar_hsa_circ_11161,RMVar_hsa_circ_344616,RMVar_hsa_circ_339409,RMVar_hsa_circ_54799,RMVar_hsa_circ_18894,RMVar_hsa_circ_63535,RMVar_hsa_circ_159464,RMVar_hsa_circ_87669,RMVar_hsa_circ_159466 5755 RMVar_ID_5755 Human_SNP_ID_514357641 A-to-I Human chr12 + 105150619 105150619 105150619 CAGCGTGGGCAACATGGCGAAACCTCATCTCTACTAATAATACCAAAATTAGCCGGGCATGGTGG CAGCGTGGGCAACATGGCGAAACCTCATCTCTGCTAATAATACCAAAATTAGCCGGGCATGGTGG A G WASHC4 Ensembl:ENSG00000136051 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1342537338 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37136,RMVar_hsa_circ_354817,RMVar_hsa_circ_42554,RMVar_hsa_circ_2601,RMVar_hsa_circ_6079,RMVar_hsa_circ_34317,RMVar_hsa_circ_344616,RMVar_hsa_circ_339409,RMVar_hsa_circ_159464,RMVar_hsa_circ_341948,RMVar_hsa_circ_108083,RMVar_hsa_circ_70568,RMVar_hsa_circ_352641,RMVar_hsa_circ_159468,RMVar_hsa_circ_57806,RMVar_hsa_circ_16195,RMVar_hsa_circ_74170,RMVar_hsa_circ_14939,RMVar_hsa_circ_54873,RMVar_hsa_circ_7055,RMVar_hsa_circ_300722,RMVar_hsa_circ_367358,RMVar_hsa_circ_299786,RMVar_hsa_circ_159474,RMVar_hsa_circ_159475 5756 RMVar_ID_5756 Human_SNP_ID_514357967 A-to-I Human chr12 + 105151656 105151656 105151656 GGTGCACACCACCACACCCAGCTAATTTTAGTATTTTTAGTAGAGATGGGGTTTCACCATATTGG GGTGCACACCACCACACCCAGCTAATTTTAGTGTTTTTAGTAGAGATGGGGTTTCACCATATTGG A G WASHC4 Ensembl:ENSG00000136051 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1285535992 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37136,RMVar_hsa_circ_354817,RMVar_hsa_circ_42554,RMVar_hsa_circ_2601,RMVar_hsa_circ_6079,RMVar_hsa_circ_34317,RMVar_hsa_circ_344616,RMVar_hsa_circ_339409,RMVar_hsa_circ_159464,RMVar_hsa_circ_341948,RMVar_hsa_circ_108083,RMVar_hsa_circ_70568,RMVar_hsa_circ_352641,RMVar_hsa_circ_159468,RMVar_hsa_circ_57806,RMVar_hsa_circ_16195,RMVar_hsa_circ_74170,RMVar_hsa_circ_14939,RMVar_hsa_circ_54873,RMVar_hsa_circ_7055,RMVar_hsa_circ_300722,RMVar_hsa_circ_367358,RMVar_hsa_circ_299786,RMVar_hsa_circ_159474,RMVar_hsa_circ_159475 5757 RMVar_ID_5757 Human_SNP_ID_514357968 A-to-I Human chr12 + 105151662 105151662 105151662 CACCACCACACCCAGCTAATTTTAGTATTTTTAGTAGAGATGGGGTTTCACCATATTGGTCAGAC CACCACCACACCCAGCTAATTTTAGTATTTTTGGTAGAGATGGGGTTTCACCATATTGGTCAGAC A G WASHC4 Ensembl:ENSG00000136051 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs543234344 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37136,RMVar_hsa_circ_354817,RMVar_hsa_circ_42554,RMVar_hsa_circ_2601,RMVar_hsa_circ_6079,RMVar_hsa_circ_34317,RMVar_hsa_circ_344616,RMVar_hsa_circ_339409,RMVar_hsa_circ_159464,RMVar_hsa_circ_341948,RMVar_hsa_circ_108083,RMVar_hsa_circ_70568,RMVar_hsa_circ_352641,RMVar_hsa_circ_159468,RMVar_hsa_circ_57806,RMVar_hsa_circ_16195,RMVar_hsa_circ_74170,RMVar_hsa_circ_14939,RMVar_hsa_circ_54873,RMVar_hsa_circ_7055,RMVar_hsa_circ_300722,RMVar_hsa_circ_367358,RMVar_hsa_circ_299786,RMVar_hsa_circ_159474,RMVar_hsa_circ_159475 5758 RMVar_ID_5758 Human_SNP_ID_514363286 A-to-I Human chr12 - 105173800 105173800 105173800 AATTGGACCTAATAGCATTTCTTTGTGCAGTTAGGTGATGAGCACTGCTTTGAGGCCCAAGCACT AATTGGACCTAATAGCATTTCTTTGTGCAGTTGGGTGATGAGCACTGCTTTGAGGCCCAAGCACT T C APPL2 Ensembl:ENSG00000136044 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1264316760 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4197768,Human_RBP_ID_6124404 RMVar_hsa_circ_110047,RMVar_hsa_circ_159480 5759 RMVar_ID_5759 Human_SNP_ID_514369503 A-to-I Human chr12 - 105195792 105195792 105195792 CCTCACCTTCCCAAAATGCTGGGACTGCAGGCATGAGCCACTGCACCTGGCCCTGGAACCCCATT CCTCACCTTCCCAAAATGCTGGGACTGCAGGCGTGAGCCACTGCACCTGGCCCTGGAACCCCATT T C APPL2 Ensembl:ENSG00000136044 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1190702597 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4600,RMVar_hsa_circ_19669,RMVar_hsa_circ_58936,RMVar_hsa_circ_110047,RMVar_hsa_circ_159480,RMVar_hsa_circ_159481,RMVar_hsa_circ_98053,RMVar_hsa_circ_371991,RMVar_hsa_circ_38627,RMVar_hsa_circ_159482,RMVar_hsa_circ_159483,RMVar_hsa_circ_337263,RMVar_hsa_circ_105673,RMVar_hsa_circ_159485 5760 RMVar_ID_5760 Human_SNP_ID_514369506 A-to-I Human chr12 - 105195809 105195809 105195809 CTCAAGCCATCCTCCTGCCTCACCTTCCCAAAATGCTGGGACTGCAGGCATGAGCCACTGCACCT CTCAAGCCATCCTCCTGCCTCACCTTCCCAAACTGCTGGGACTGCAGGCATGAGCCACTGCACCT T G APPL2 Ensembl:ENSG00000136044 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1371149836 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4600,RMVar_hsa_circ_19669,RMVar_hsa_circ_58936,RMVar_hsa_circ_110047,RMVar_hsa_circ_159480,RMVar_hsa_circ_159481,RMVar_hsa_circ_98053,RMVar_hsa_circ_371991,RMVar_hsa_circ_38627,RMVar_hsa_circ_159482,RMVar_hsa_circ_159483,RMVar_hsa_circ_337263,RMVar_hsa_circ_105673,RMVar_hsa_circ_159485 5761 RMVar_ID_5761 Human_SNP_ID_514369507 A-to-I Human chr12 - 105195810 105195810 105195810 GCTCAAGCCATCCTCCTGCCTCACCTTCCCAAAATGCTGGGACTGCAGGCATGAGCCACTGCACC GCTCAAGCCATCCTCCTGCCTCACCTTCCCAAGATGCTGGGACTGCAGGCATGAGCCACTGCACC T C APPL2 Ensembl:ENSG00000136044 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1202622194 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4600,RMVar_hsa_circ_19669,RMVar_hsa_circ_58936,RMVar_hsa_circ_110047,RMVar_hsa_circ_159480,RMVar_hsa_circ_159481,RMVar_hsa_circ_98053,RMVar_hsa_circ_371991,RMVar_hsa_circ_38627,RMVar_hsa_circ_159482,RMVar_hsa_circ_159483,RMVar_hsa_circ_337263,RMVar_hsa_circ_105673,RMVar_hsa_circ_159485 5762 RMVar_ID_5762 Human_SNP_ID_514615392 A-to-I Human chr12 - 106238360 106238360 106238360 GCAAAGCATCCAGGCGGTTCTGAATGTGAAGCACTACACCCAGCAGAGTCCCGGTGCCCTCTGTC GCAAAGCATCCAGGCGGTTCTGAATGTGAAGCCCTACACCCAGCAGAGTCCCGGTGCCCTCTGTC T G CKAP4 Ensembl:ENSG00000136026 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs139021046 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_409078,Human_RBP_ID_1785598,Human_RBP_ID_4249150,Human_RBP_ID_8178709,Human_RBP_ID_8363899,Human_RBP_ID_11791575,Human_RBP_ID_17242975,Human_RBP_ID_17467705,Human_RBP_ID_17831507,Human_RBP_ID_18254552,Human_RBP_ID_23533910,Human_RBP_ID_24463785 Human_miRNA_ID_291478,Human_miRNA_ID_1510855,Human_miRNA_ID_1641136 5763 RMVar_ID_5763 Human_SNP_ID_514637770 A-to-I Human chr12 + 106327319 106327319 106327319 GGACTCAAGGGATTCTCCTGTCTCAGCTTCCCAAGTAGCTAGGACTACAGGCATGTGCCACCACG GGACTCAAGGGATTCTCCTGTCTCAGCTTCCCGAGTAGCTAGGACTACAGGCATGTGCCACCACG A G TCP11L2 Ensembl:ENSG00000166046 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs894403813 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94218,RMVar_hsa_circ_62612,RMVar_hsa_circ_74242,RMVar_hsa_circ_159512 5764 RMVar_ID_5764 Human_SNP_ID_514785952 A-to-I Human chr12 + 106967358 106967358 106967358 TTGGCCCACTGCAACCTCCGCTTCCTGGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCCAAGTAGC TTGGCCCACTGCAACCTCCGCTTCCTGGGTTCGAGCAGTTCTCCTGCCTCAGCCTCCCAAGTAGC A G TMEM263 Ensembl:ENSG00000151135 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1023544301 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1418812,Human_Splice_Rec_1418813 5765 RMVar_ID_5765 Human_SNP_ID_514788372 A-to-I Human chr12 - 106978008 106978008 106978008 AGCTATAAAGGAAACACTAGAATTTCTCCAGGAGCAAGGTTTCACCAGCTTTGAAATTCTCCAGC AGCTATAAAGGAAACACTAGAATTTCTCCAGGGGCAAGGTTTCACCAGCTTTGAAATTCTCCAGC T C MTERF2 Ensembl:ENSG00000120832 Protein coding CDS GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs753627218 Functional Loss SNV dbSNP153 33..33 33 - - - 5766 RMVar_ID_5766 Human_SNP_ID_514961438 A-to-I Human chr12 + 107698827 107698827 107698827 GTTGCCTGGGCTGGTCTCGAACTCCCGGCCTCAAGCGATGTTCCCACGTTAGCTTCCCAAGGTCC GTTGCCTGGGCTGGTCTCGAACTCCCGGCCTCCAGCGATGTTCCCACGTTAGCTTCCCAAGGTCC A C PWP1 Ensembl:ENSG00000136045 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1346175249 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114180,RMVar_hsa_circ_317567,RMVar_hsa_circ_287745,RMVar_hsa_circ_159585 5767 RMVar_ID_5767 Human_SNP_ID_514961493 A-to-I Human chr12 + 107699049 107699049 107699049 ACTTTGGGAGGCCGAGAGTGGATCATGAGGTCAGGAGTTCCTGACCACCCTGGCCAACGTGGCAA ACTTTGGGAGGCCGAGAGTGGATCATGAGGTCTGGAGTTCCTGACCACCCTGGCCAACGTGGCAA A T PWP1 Ensembl:ENSG00000136045 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1047820426 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114180,RMVar_hsa_circ_317567,RMVar_hsa_circ_287745,RMVar_hsa_circ_159585 5768 RMVar_ID_5768 Human_SNP_ID_514973486 A-to-I Human chr12 - 107747064 107747063 107747064 TACCCCAGGCTGGTCTTGAACTCCTGGACTCAAGTGATCCTCCCTTCTCAGCCTCCCAAACTGCT TACCCCAGGCTGGTCTTGAACTCCTGGACTCA_GTGATCCTCCCTTCTCAGCCTCCCAAACTGCT CT C PRDM4 Ensembl:ENSG00000110851 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1252456004 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_94769,RMVar_hsa_circ_44036,RMVar_hsa_circ_159594,RMVar_hsa_circ_65672,RMVar_hsa_circ_159592,RMVar_hsa_circ_371055,RMVar_hsa_circ_269399,RMVar_hsa_circ_286798,RMVar_hsa_circ_159596 5769 RMVar_ID_5769 Human_SNP_ID_514974123 A-to-I Human chr12 - 107749507 107749507 107749507 GTAGAGAAGGCCATGTGTTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGAAAG GTAGAGAAGGCCATGTGTTGGCTCACACCTGTGATCCCAGCACTTTGGGAGGCTGAGGCAGAAAG T C PRDM4 Ensembl:ENSG00000110851 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs117732799 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94769,RMVar_hsa_circ_44036,RMVar_hsa_circ_159594,RMVar_hsa_circ_65672,RMVar_hsa_circ_159592,RMVar_hsa_circ_371055,RMVar_hsa_circ_269399,RMVar_hsa_circ_286798,RMVar_hsa_circ_159596 5770 RMVar_ID_5770 Human_SNP_ID_514974124 A-to-I Human chr12 - 107749513 107749513 107749513 AGGTAAGTAGAGAAGGCCATGTGTTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGC AGGTAAGTAGAGAAGGCCATGTGTTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGC T C PRDM4 Ensembl:ENSG00000110851 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037258089 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94769,RMVar_hsa_circ_44036,RMVar_hsa_circ_159594,RMVar_hsa_circ_65672,RMVar_hsa_circ_159592,RMVar_hsa_circ_371055,RMVar_hsa_circ_269399,RMVar_hsa_circ_286798,RMVar_hsa_circ_159596 5771 RMVar_ID_5771 Human_SNP_ID_515166702 A-to-I Human chr12 - 108526829 108526829 108526829 GGAATTTGCCTTCTGAACTTTGAGATCCACTGACCTTTTGTATAATTAAGAGTGGACAATGGGGA GGAATTTGCCTTCTGAACTTTGAGATCCACTGGCCTTTTGTATAATTAAGAGTGGACAATGGGGA T C SART3 Ensembl:ENSG00000075856 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4964716 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11795893 RMVar_hsa_circ_44654,RMVar_hsa_circ_364089,RMVar_hsa_circ_364163 5772 RMVar_ID_5772 Human_SNP_ID_515166946 A-to-I Human chr12 - 108527984 108527984 108527984 GAGGTGGGCGGATCACCTGAGGTCAGGGGTCAAGATCAACCTGGCCAACATGGTGAAAACCTGCC GAGGTGGGCGGATCACCTGAGGTCAGGGGTCAGGATCAACCTGGCCAACATGGTGAAAACCTGCC T C SART3 Ensembl:ENSG00000075856 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs986571802 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44654,RMVar_hsa_circ_364089,RMVar_hsa_circ_364163 5773 RMVar_ID_5773 Human_SNP_ID_515170051 A-to-I Human chr12 - 108540404 108540404 108540404 GTCTTCAACACTTGACCTTTAGAGTCCCCTGCAAGGGAGATTTGCTGGTAACAGATTTTCTGTGT GTCTTCAACACTTGACCTTTAGAGTCCCCTGCTAGGGAGATTTGCTGGTAACAGATTTTCTGTGT T A SART3 Ensembl:ENSG00000075856 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10861940 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_261 RMVar_hsa_circ_364089,RMVar_hsa_circ_364163,RMVar_hsa_circ_68805,RMVar_hsa_circ_365849,RMVar_hsa_circ_22333,RMVar_hsa_circ_31176,RMVar_hsa_circ_60236,RMVar_hsa_circ_47264,RMVar_hsa_circ_22139,RMVar_hsa_circ_72240 5774 RMVar_ID_5774 Human_SNP_ID_515170052 A-to-I Human chr12 - 108540404 108540404 108540404 GTCTTCAACACTTGACCTTTAGAGTCCCCTGCAAGGGAGATTTGCTGGTAACAGATTTTCTGTGT GTCTTCAACACTTGACCTTTAGAGTCCCCTGCGAGGGAGATTTGCTGGTAACAGATTTTCTGTGT T C SART3 Ensembl:ENSG00000075856 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10861940 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_261 RMVar_hsa_circ_364089,RMVar_hsa_circ_364163,RMVar_hsa_circ_68805,RMVar_hsa_circ_365849,RMVar_hsa_circ_22333,RMVar_hsa_circ_31176,RMVar_hsa_circ_60236,RMVar_hsa_circ_47264,RMVar_hsa_circ_22139,RMVar_hsa_circ_72240 5775 RMVar_ID_5775 Human_SNP_ID_515170053 A-to-I Human chr12 - 108540404 108540404 108540404 GTCTTCAACACTTGACCTTTAGAGTCCCCTGCAAGGGAGATTTGCTGGTAACAGATTTTCTGTGT GTCTTCAACACTTGACCTTTAGAGTCCCCTGCCAGGGAGATTTGCTGGTAACAGATTTTCTGTGT T G SART3 Ensembl:ENSG00000075856 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10861940 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_261 RMVar_hsa_circ_364089,RMVar_hsa_circ_364163,RMVar_hsa_circ_68805,RMVar_hsa_circ_365849,RMVar_hsa_circ_22333,RMVar_hsa_circ_31176,RMVar_hsa_circ_60236,RMVar_hsa_circ_47264,RMVar_hsa_circ_22139,RMVar_hsa_circ_72240 5776 RMVar_ID_5776 Human_SNP_ID_515171347 A-to-I Human chr12 - 108545783 108545783 108545783 TTTTCTATTTTTAGTAGAGACGGGGTTTCACCATATTGGCCAGGCTGGTTTCGATCTCCTGACCT TTTTCTATTTTTAGTAGAGACGGGGTTTCACCGTATTGGCCAGGCTGGTTTCGATCTCCTGACCT T C SART3 Ensembl:ENSG00000075856 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1248100761 Functional Loss SNV dbSNP153 33..33 33 - - - 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 5777 RMVar_ID_5777 Human_SNP_ID_515171515 A-to-I Human chr12 - 108546328 108546328 108546328 AGGCGTGGTGGCATGCTCCTGTTGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATTGCTTGAA AGGCGTGGTGGCATGCTCCTGTTGTCCCAGCTGCTTGGGAGGCTGAGGCAGGAGAATTGCTTGAA T C SART3 Ensembl:ENSG00000075856 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs889892532 Functional Loss SNV dbSNP153 33..33 33 - - - 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 5778 RMVar_ID_5778 Human_SNP_ID_515171609 A-to-I Human chr12 - 108546722 108546722 108546722 GAGCCCAGGAGTTCGAAATCAGCCTGCCCAACATGGGGAAAACCCCATCTCCACTAAAAATACAA GAGCCCAGGAGTTCGAAATCAGCCTGCCCAACGTGGGGAAAACCCCATCTCCACTAAAAATACAA T C SART3 Ensembl:ENSG00000075856 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs774744744 Functional Loss SNV dbSNP153 33..33 33 - - - 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 5779 RMVar_ID_5779 Human_SNP_ID_515173681 A-to-I Human chr12 - 108555541 108555541 108555541 TTCACCTCAGCCTTTCGAGTAGCTGGGACCACAGGCATGTGCCACCAGACTCAGCTAATTTTTAC TTCACCTCAGCCTTTCGAGTAGCTGGGACCACGGGCATGTGCCACCAGACTCAGCTAATTTTTAC T C SART3 Ensembl:ENSG00000075856 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1183006566 Functional Loss SNV dbSNP153 33..33 33 - - - 5780 RMVar_ID_5780 Human_SNP_ID_515211323 A-to-I Human chr12 - 108706763 108706763 108706763 TCTGACCAACATAGTGAAACCCTGTCTCTGCTAAAAATACAAAAATTAGCTGGGTGCAGTGTAGT TCTGACCAACATAGTGAAACCCTGTCTCTGCTTAAAATACAAAAATTAGCTGGGTGCAGTGTAGT T A CORO1C Ensembl:ENSG00000110880 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444923834 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98336,RMVar_hsa_circ_159621,RMVar_hsa_circ_110657,RMVar_hsa_circ_159622,RMVar_hsa_circ_76550,RMVar_hsa_circ_159639 5781 RMVar_ID_5781 Human_SNP_ID_515211341 A-to-I Human chr12 - 108706870 108706870 108706870 TATGATTTTATAAAAATACGGCTAGGCATGGTAGCTCACACCTGTAATCCCAGCACTTTGTGAGG TATGATTTTATAAAAATACGGCTAGGCATGGTGGCTCACACCTGTAATCCCAGCACTTTGTGAGG T C CORO1C Ensembl:ENSG00000110880 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1019722508 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98336,RMVar_hsa_circ_159621,RMVar_hsa_circ_110657,RMVar_hsa_circ_159622,RMVar_hsa_circ_76550,RMVar_hsa_circ_159639 5782 RMVar_ID_5782 Human_SNP_ID_515211346 A-to-I Human chr12 - 108706879 108706879 108706879 ATTGTTTGTTATGATTTTATAAAAATACGGCTAGGCATGGTAGCTCACACCTGTAATCCCAGCAC ATTGTTTGTTATGATTTTATAAAAATACGGCTCGGCATGGTAGCTCACACCTGTAATCCCAGCAC T G CORO1C Ensembl:ENSG00000110880 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs972784828 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98336,RMVar_hsa_circ_159621,RMVar_hsa_circ_110657,RMVar_hsa_circ_159622,RMVar_hsa_circ_76550,RMVar_hsa_circ_159639 5783 RMVar_ID_5783 Human_SNP_ID_515231320 A-to-I Human chr12 - 108791248 108791248 108791248 AAAATTAGCTGGGTGTGATGGTGCATGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCACGAGA AAAATTAGCTGGGTGTGATGGTGCATGCCTGTGATCCCAGCTACTCAGGAGGCTGAGGCACGAGA T C SSH1 Ensembl:ENSG00000084112 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1232368883 Functional Loss SNV dbSNP153 33..33 33 - - - 5784 RMVar_ID_5784 Human_SNP_ID_515231422 A-to-I Human chr12 - 108791637 108791637 108791637 CTCCTACCTCAGCCTCCTGAGTAGCTGGGACCACAGGCGCATGCTACCACACCCGGTTAATCTTT CTCCTACCTCAGCCTCCTGAGTAGCTGGGACCGCAGGCGCATGCTACCACACCCGGTTAATCTTT T C SSH1 Ensembl:ENSG00000084112 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1275734992 Functional Loss SNV dbSNP153 33..33 33 - - - 5785 RMVar_ID_5785 Human_SNP_ID_515231433 A-to-I Human chr12 - 108791664 108791664 108791664 GCCTTGACCTCCCAGGCTCAAGTGATCCTCCTACCTCAGCCTCCTGAGTAGCTGGGACCACAGGC GCCTTGACCTCCCAGGCTCAAGTGATCCTCCTGCCTCAGCCTCCTGAGTAGCTGGGACCACAGGC T C SSH1 Ensembl:ENSG00000084112 Protein coding intron GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line - 24183664,31158229 RNA-Seq:(High) rs572066582 Functional Loss SNV dbSNP153 33..33 33 - - - 5786 RMVar_ID_5786 Human_SNP_ID_515231452 A-to-I Human chr12 - 108791743 108791740 108791744 TATAGATAGATACATACTATAGACAAGTTCTCACTGTTTCCCATGCTGGAGTACAGTGGCATGAT TATAGATAGATACATACTATAGACAAGTTCT____GTTTCCCATGCTGGAGTACAGTGGCATGAT CAGTG C SSH1 Ensembl:ENSG00000084112 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1291846216 Functional Loss DEL dbSNP153 32..35 33 - - - 5787 RMVar_ID_5787 Human_SNP_ID_515237399 A-to-I Human chr12 - 108812991 108812991 108812991 GGGCATAGTGGCATGTGCCTGTGGTCCTAGCTACTCAGGAGGCTGAGGTGGGAGGATTGATTAGG GGGCATAGTGGCATGTGCCTGTGGTCCTAGCTGCTCAGGAGGCTGAGGTGGGAGGATTGATTAGG T C SSH1 Ensembl:ENSG00000084112 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900978042 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_159641,RMVar_hsa_circ_373889,RMVar_hsa_circ_81949,RMVar_hsa_circ_159642,RMVar_hsa_circ_44566,RMVar_hsa_circ_25518,RMVar_hsa_circ_159645,RMVar_hsa_circ_159644,RMVar_hsa_circ_114166,RMVar_hsa_circ_4564,RMVar_hsa_circ_303883 5788 RMVar_ID_5788 Human_SNP_ID_515241694 A-to-I Human chr12 - 108829858 108829858 108829858 GGGTCAACTGATTCTCCCACTTTGACCTCCCAAAGTGCTGTGATTACAGGCATGAGCTACCATGC GGGTCAACTGATTCTCCCACTTTGACCTCCCAGAGTGCTGTGATTACAGGCATGAGCTACCATGC T C SSH1 Ensembl:ENSG00000084112 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs551106924 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13798,RMVar_hsa_circ_4564,RMVar_hsa_circ_327782,RMVar_hsa_circ_159652 5789 RMVar_ID_5789 Human_SNP_ID_515246662 A-to-I Human chr12 - 108849457 108849457 108849457 GAACTCCTGGGGCCAAGCTATCTTCCCACCTCAGCCTCCCAAGTAGCTGGGACTACAGGCGTGCG GAACTCCTGGGGCCAAGCTATCTTCCCACCTCTGCCTCCCAAGTAGCTGGGACTACAGGCGTGCG T A SSH1 Ensembl:ENSG00000084112 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs554932428 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13798,RMVar_hsa_circ_4564,RMVar_hsa_circ_327782,RMVar_hsa_circ_159652 5790 RMVar_ID_5790 Human_SNP_ID_515247475 A-to-I Human chr12 - 108852344 108852344 108852344 TGTGCTTGTAGTCCCAGCTACTTGGGGGGCTGAGGCGGGGGAATCGCTTGAACCCGGGAGGCAGA TGTGCTTGTAGTCCCAGCTACTTGGGGGGCTGGGGCGGGGGAATCGCTTGAACCCGGGAGGCAGA T C SSH1 Ensembl:ENSG00000084112 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1007758829 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13798,RMVar_hsa_circ_4564,RMVar_hsa_circ_327782,RMVar_hsa_circ_159652 5791 RMVar_ID_5791 Human_SNP_ID_515297217 A-to-I Human chr12 + 109054410 109054410 109054410 TGGGCATGTGGTGTGCAGCTGTGGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGGATCACCTGAG TGGGCATGTGGTGTGCAGCTGTGGTCCCAGCTCCTTGGGAGGCTGAGGCAGGAGGATCACCTGAG A C USP30 Ensembl:ENSG00000135093 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1271455421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24925797 RMVar_hsa_circ_77775,RMVar_hsa_circ_159667 5792 RMVar_ID_5792 Human_SNP_ID_515298531 A-to-I Human chr12 + 109059294 109059294 109059294 TCAGCTCACTGCAACCTTCACCTCTCAGGTTCAAGTGATTCTTGTGCCTCAGCCTCCTGAGTAGC TCAGCTCACTGCAACCTTCACCTCTCAGGTTCCAGTGATTCTTGTGCCTCAGCCTCCTGAGTAGC A C USP30 Ensembl:ENSG00000135093 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1050779382 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2277,RMVar_hsa_circ_77775,RMVar_hsa_circ_159667 5793 RMVar_ID_5793 Human_SNP_ID_515298618 A-to-I Human chr12 + 109059688 109059688 109059688 GCTGCATGCCACCACGCCCGGCTAATGTTTGTATTTTTAGTAGAGACAGTGTTCGCCATGTTAGC GCTGCATGCCACCACGCCCGGCTAATGTTTGTGTTTTTAGTAGAGACAGTGTTCGCCATGTTAGC A G USP30 Ensembl:ENSG00000135093 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs988488707 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2277,RMVar_hsa_circ_77775,RMVar_hsa_circ_159667 5794 RMVar_ID_5794 Human_SNP_ID_515306008 A-to-I Human chr12 - 109091201 109091201 109091201 TTAAATTATCTGTAGGTCTCACTGTGTTACCCAGGCTGTTAATTGAACTCCTGGCCTTGAGTGAT TTAAATTATCTGTAGGTCTCACTGTGTTACCCCGGCTGTTAATTGAACTCCTGGCCTTGAGTGAT T G ALKBH2 Ensembl:ENSG00000189046 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1233348720 Functional Loss SNV dbSNP153 33..33 33 - - - 5795 RMVar_ID_5795 Human_SNP_ID_515309870 A-to-I Human chr12 + 109104185 109104185 109104185 ATTCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCCGCCACCACACCCGGCTGATTTTT ATTCTGCCTCAGCCTCCCGAGTAGCTGGGACTGCAGGCGCCCGCCACCACACCCGGCTGATTTTT A G UNG Ensembl:ENSG00000076248 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1335930026 Functional Loss SNV dbSNP153 33..33 33 - - - 5796 RMVar_ID_5796 Human_SNP_ID_515310123 A-to-I Human chr12 + 109105122 109105122 109105122 TTTTAGTAGAGACTGGGTTTCACCATGTTGACAAGGCTGGTCTTGAACTCCTGACCTCAAGCGAT TTTTAGTAGAGACTGGGTTTCACCATGTTGACGAGGCTGGTCTTGAACTCCTGACCTCAAGCGAT A G UNG Ensembl:ENSG00000076248 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1398244258 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1420508,Human_Splice_Rec_1420509 5797 RMVar_ID_5797 Human_SNP_ID_515310130 A-to-I Human chr12 + 109105182 109105182 109105182 GCGATCCTCCCATCTTGGTCTCCCAAAGTGCTAGGATTACAGATGTAAGCCACCGCACCCGACCA GCGATCCTCCCATCTTGGTCTCCCAAAGTGCTGGGATTACAGATGTAAGCCACCGCACCCGACCA A G UNG Ensembl:ENSG00000076248 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1057387519 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1420508,Human_Splice_Rec_1420509 5798 RMVar_ID_5798 Human_SNP_ID_515310134 A-to-I Human chr12 + 109105196 109105189 109105196 TTGGTCTCCCAAAGTGCTAGGATTACAGATGTAAGCCACCGCACCCGACCAGGTTGAGTACTTTG TTGGTCTCCCAAAGTGCTAGGATTAC_______AGCCACCGCACCCGACCAGGTTGAGTACTTTG CAGATGTA C UNG Ensembl:ENSG00000076248 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1305547601 Functional Loss DEL dbSNP153 27..33 33 - - - Human_Splice_Rec_1420509 5799 RMVar_ID_5799 Human_SNP_ID_515310308 A-to-I Human chr12 + 109105909 109105900 109105909 CTTAGGCTGAAGATCTGATTTCAGGGGGGTAGAGGGGTGGCCCCCAATCGGCCTCCCAGACTTAA CTTAGGCTGAAGATCTGATTTCAG_________GGGGTGGCCCCCAATCGGCCTCCCAGACTTAA GGGGGGTAGA G UNG Ensembl:ENSG00000076248 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1374310034 Functional Loss DEL dbSNP153 25..33 33 - - - 5800 RMVar_ID_5800 Human_SNP_ID_515310314 A-to-I Human chr12 + 109105909 109105908 109105909 CTTAGGCTGAAGATCTGATTTCAGGGGGGTAGAGGGGTGGCCCCCAATCGGCCTCCCAGACTTAA CTTAGGCTGAAGATCTGATTTCAGGGGGGTAG_GGGGTGGCCCCCAATCGGCCTCCCAGACTTAA GA G UNG Ensembl:ENSG00000076248 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs574661862 Functional Loss DEL dbSNP153 33..33 33 - - - 5801 RMVar_ID_5801 Human_SNP_ID_515310316 A-to-I Human chr12 + 109105909 109105909 109105909 CTTAGGCTGAAGATCTGATTTCAGGGGGGTAGAGGGGTGGCCCCCAATCGGCCTCCCAGACTTAA CTTAGGCTGAAGATCTGATTTCAGGGGGGTAGCGGGGTGGCCCCCAATCGGCCTCCCAGACTTAA A C UNG Ensembl:ENSG00000076248 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs246078 Functional Loss SNV dbSNP153 33..33 33 - - - 5802 RMVar_ID_5802 Human_SNP_ID_515310317 A-to-I Human chr12 + 109105909 109105909 109105909 CTTAGGCTGAAGATCTGATTTCAGGGGGGTAGAGGGGTGGCCCCCAATCGGCCTCCCAGACTTAA CTTAGGCTGAAGATCTGATTTCAGGGGGGTAGGGGGGTGGCCCCCAATCGGCCTCCCAGACTTAA A G UNG Ensembl:ENSG00000076248 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs246078 Functional Loss SNV dbSNP153 33..33 33 - - - 5803 RMVar_ID_5803 Human_SNP_ID_515310536 A-to-I Human chr12 + 109106817 109106817 109106817 GCTACTTGGGAGGCAGAGGTTGCAGTTAGCTGAGATCATGCCACTGCACTCCAGCCTGGCAACAG GCTACTTGGGAGGCAGAGGTTGCAGTTAGCTGGGATCATGCCACTGCACTCCAGCCTGGCAACAG A G UNG Ensembl:ENSG00000076248 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1279449694 Functional Loss SNV dbSNP153 33..33 33 - - - 5804 RMVar_ID_5804 Human_SNP_ID_515310798 A-to-I Human chr12 + 109107330 109107330 109107330 TCAAGCAATCCTCCCACCTTAGTCACCTGAGTAGCAGGGACCACAGGCGTGCGCCACCACACCTG TCAAGCAATCCTCCCACCTTAGTCACCTGAGTTGCAGGGACCACAGGCGTGCGCCACCACACCTG A T UNG Ensembl:ENSG00000076248 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1199160354 Functional Loss SNV dbSNP153 33..33 33 - - - 5805 RMVar_ID_5805 Human_SNP_ID_515311122 A-to-I Human chr12 + 109108557 109108557 109108557 AGGAGGCTGAGGTGGGAGAGTAACTTGAGCCTAGGAGGTGGAGGCTACAGTGGGCCACAGTCATG AGGAGGCTGAGGTGGGAGAGTAACTTGAGCCTGGGAGGTGGAGGCTACAGTGGGCCACAGTCATG A G UNG Ensembl:ENSG00000076248 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1046257625 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17808507 5806 RMVar_ID_5806 Human_SNP_ID_515311177 A-to-I Human chr12 + 109108760 109108760 109108760 TCAAGTGATCCTGCCACCTCAGTCTTCTGTGTAGCTAGGACTGCAGGTGCATGCCATCACACTTG TCAAGTGATCCTGCCACCTCAGTCTTCTGTGTGGCTAGGACTGCAGGTGCATGCCATCACACTTG A G UNG Ensembl:ENSG00000076248 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1286570590 Functional Loss SNV dbSNP153 33..33 33 - - - 5807 RMVar_ID_5807 Human_SNP_ID_515311407 A-to-I Human chr12 + 109109602 109109602 109109602 GTCAAGAGATCGAGACCATCCTGGCCAATATGATGAAACCCCATCTCTACTAAAAATACAAAAAT GTCAAGAGATCGAGACCATCCTGGCCAATATGGTGAAACCCCATCTCTACTAAAAATACAAAAAT A G UNG Ensembl:ENSG00000076248 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs574248526 Functional Loss SNV dbSNP153 33..33 33 - - - 5808 RMVar_ID_5808 Human_SNP_ID_515398778 A-to-I Human chr12 - 109452955 109452955 109452955 GAACCTGGTCTGTGAATCAAGAAACAGTTGGGATCAGACCATGTGGTCTCTAAATCCCCTTGCTC GAACCTGGTCTGTGAATCAAGAAACAGTTGGGGTCAGACCATGTGGTCTCTAAATCCCCTTGCTC T C KCTD10 Ensembl:ENSG00000110906 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1308074855 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_409919 5809 RMVar_ID_5809 Human_SNP_ID_515398814 A-to-I Human chr12 - 109453113 109453113 109453113 AAGGCTGCAGTGAGCTATGATTGTGCCACTGCACTCCAGCCTGGGTGACAGAGCAACACTCCCTC AAGGCTGCAGTGAGCTATGATTGTGCCACTGCGCTCCAGCCTGGGTGACAGAGCAACACTCCCTC T C KCTD10 Ensembl:ENSG00000110906 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1292390221 Functional Loss SNV dbSNP153 33..33 33 - - - 5810 RMVar_ID_5810 Human_SNP_ID_515398848 A-to-I Human chr12 - 109453288 109453288 109453288 CTACTTGGGAGGCTGAGGTGGGAGAATCATTTAAGCCCAGTAGTTCAAGACCAGCCTGGGCAACA CTACTTGGGAGGCTGAGGTGGGAGAATCATTTGAGCCCAGTAGTTCAAGACCAGCCTGGGCAACA T C KCTD10 Ensembl:ENSG00000110906 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs571314732 Functional Loss SNV dbSNP153 33..33 33 - - - 5811 RMVar_ID_5811 Human_SNP_ID_515398855 A-to-I Human chr12 - 109453328 109453328 109453328 AAAAATAGCTGGGCATGGTGGTGTGTGCCTGTAGTCTAAACTACTTGGGAGGCTGAGGTGGGAGA AAAAATAGCTGGGCATGGTGGTGTGTGCCTGTGGTCTAAACTACTTGGGAGGCTGAGGTGGGAGA T C KCTD10 Ensembl:ENSG00000110906 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1274542101 Functional Loss SNV dbSNP153 33..33 33 - - - 5812 RMVar_ID_5812 Human_SNP_ID_515499278 A-to-I Human chr12 - 109851752 109851752 109851752 CTACTAAAAATATAGAATTAGCCAGGCATGGTAGCGCACGCCTGTAATCCCATCTTCTTGGGAGG CTACTAAAAATATAGAATTAGCCAGGCATGGTGGCGCACGCCTGTAATCCCATCTTCTTGGGAGG T C GLTP Ensembl:ENSG00000139433 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1448477152 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_410016 5813 RMVar_ID_5813 Human_SNP_ID_515499302 A-to-I Human chr12 - 109851849 109851847 109851849 GAGCGAAACTCTGTCTCAAAAAAAAAAAAAAGAGGTGGGTGGATTACTTGAGGTCAGGGTTTGAG GAGCGAAACTCTGTCTCAAAAAAAAAAAAAAG__GTGGGTGGATTACTTGAGGTCAGGGTTTGAG CCT C GLTP Ensembl:ENSG00000139433 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1376275372 Functional Loss DEL dbSNP153 33..34 33 - - - 5814 RMVar_ID_5814 Human_SNP_ID_515499956 A-to-I Human chr12 - 109854308 109854308 109854308 TCGCCCAGGCTGGAGTGCAGTGGCACAGTCTTAGCTTACCGCAACCTCCACTTCCCAGGCTCAAG TCGCCCAGGCTGGAGTGCAGTGGCACAGTCTTGGCTTACCGCAACCTCCACTTCCCAGGCTCAAG T C GLTP Ensembl:ENSG00000139433 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1298274088 Functional Loss SNV dbSNP153 33..33 33 - - - 5815 RMVar_ID_5815 Human_SNP_ID_515503608 A-to-I Human chr12 - 109869935 109869935 109869935 GTTCGAGATATGGTGAAACCTTGTCTCTTTTAAAAATACAAAAATTAGCCAGGCATGGTGGCACA GTTCGAGATATGGTGAAACCTTGTCTCTTTTACAAATACAAAAATTAGCCAGGCATGGTGGCACA T G GLTP Ensembl:ENSG00000139433 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs936123562 Functional Loss SNV dbSNP153 33..33 33 - - - 5816 RMVar_ID_5816 Human_SNP_ID_515520818 A-to-I Human chr12 - 109940623 109940598 109940623 TGCCCACCTCTGCCTCCCAACATGCTGGGATTATGGGTGTGAGCCACCGCACCTGGCCATGTAGA TGCCCACCTCTGCCTCCCAACATGCTGGGATT_________________________CATGTAGA GGCCAGGTGCGGTGGCTCACACCCAT G GIT2 Ensembl:ENSG00000139436 Protein coding intron GSE38233;GSE100210;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,frontal_cortex - 24183664,29129909,30559470 RNA-Seq:(High) rs1238257788 Functional Loss DEL dbSNP153 33..57 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 5817 RMVar_ID_5817 Human_SNP_ID_515520867 A-to-I Human chr12 - 109940816 109940816 109940816 GGAGTGCAGTAGTACGATCTCATCTCACTGCAACCTCCGCCTCCTAGGCTCAAGAGATCATCTCA GGAGTGCAGTAGTACGATCTCATCTCACTGCAGCCTCCGCCTCCTAGGCTCAAGAGATCATCTCA T C GIT2 Ensembl:ENSG00000139436 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1255216151 Functional Loss SNV dbSNP153 33..33 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 5818 RMVar_ID_5818 Human_SNP_ID_515521129 A-to-I Human chr12 - 109941694 109941694 109941694 CAACATAGTGAAACCCCATCTCTACTAAAAATACAAAATTAGCTCGGTATGGTGGTGCATGCCTG CAACATAGTGAAACCCCATCTCTACTAAAAATGCAAAATTAGCTCGGTATGGTGGTGCATGCCTG T C GIT2 Ensembl:ENSG00000139436 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs539077624 Functional Loss SNV dbSNP153 33..33 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 5819 RMVar_ID_5819 Human_SNP_ID_515521149 A-to-I Human chr12 - 109941796 109941796 109941796 AAAAAATTGGCAGGGTGCGGTGGCTCACACCTATAATCTCAGCACTTTTGGAGGCTGAGGCGGGA AAAAAATTGGCAGGGTGCGGTGGCTCACACCTGTAATCTCAGCACTTTTGGAGGCTGAGGCGGGA T C GIT2 Ensembl:ENSG00000139436 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs887713130 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24926447 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 5820 RMVar_ID_5820 Human_SNP_ID_515521300 A-to-I Human chr12 - 109942406 109942406 109942406 TCACTTGAACCTGGGAGGCCGAGGCAGAAGTTACAGTGATCCAGGATTGCACCACTGCACTCCAG TCACTTGAACCTGGGAGGCCGAGGCAGAAGTTGCAGTGATCCAGGATTGCACCACTGCACTCCAG T C GIT2 Ensembl:ENSG00000139436 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982754748 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11800923 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 5821 RMVar_ID_5821 Human_SNP_ID_515521309 A-to-I Human chr12 - 109942449 109942449 109942449 GGTGCCTGTAGTCCCAGCTACTTGGGAGGCTTAGGCAGGAGAATCACTTGAACCTGGGAGGCCGA GGTGCCTGTAGTCCCAGCTACTTGGGAGGCTTGGGCAGGAGAATCACTTGAACCTGGGAGGCCGA T C GIT2 Ensembl:ENSG00000139436 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1211345193 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24926462 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 5822 RMVar_ID_5822 Human_SNP_ID_515521658 A-to-I Human chr12 - 109944115 109944115 109944115 ACAATAGCTATTTACAGGCATGGTCATAGCGTACTGCAGCCTCAAACTCCTGGGCTCAAGCAGTC ACAATAGCTATTTACAGGCATGGTCATAGCGTGCTGCAGCCTCAAACTCCTGGGCTCAAGCAGTC T C GIT2 Ensembl:ENSG00000139436 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs954635042 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11800951,Human_RBP_ID_17561260 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 5823 RMVar_ID_5823 Human_SNP_ID_515521668 A-to-I Human chr12 - 109944174 109944173 109944175 ATTCGTTTTTTTATTTTTTATTTTTTAGAGACAGAGTCTCATGTTGCCCAGTCTGTAGTACAATA ATTCGTTTTTTTATTTTTTATTTTTTAGAGA__GAGTCTCATGTTGCCCAGTCTGTAGTACAATA CTG C GIT2 Ensembl:ENSG00000139436 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs772868301 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_11800955 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 5824 RMVar_ID_5824 Human_SNP_ID_515523644 A-to-I Human chr12 - 109953558 109953558 109953558 CAGTGGTGCAGTCATGGTTCACTGCAGCCTCAATCTCCTGGGCTCAAGCAATCCTCCTGTCTTAG CAGTGGTGCAGTCATGGTTCACTGCAGCCTCAGTCTCCTGGGCTCAAGCAATCCTCCTGTCTTAG T C GIT2 Ensembl:ENSG00000139436 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1384055441 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20382,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_159745,RMVar_hsa_circ_30936,RMVar_hsa_circ_159744,RMVar_hsa_circ_345919,RMVar_hsa_circ_83049,RMVar_hsa_circ_335714,RMVar_hsa_circ_362494,RMVar_hsa_circ_106891,RMVar_hsa_circ_57464,RMVar_hsa_circ_159746,RMVar_hsa_circ_159747,RMVar_hsa_circ_37991,RMVar_hsa_circ_14539,RMVar_hsa_circ_16135,RMVar_hsa_circ_66797,RMVar_hsa_circ_343068,RMVar_hsa_circ_71444,RMVar_hsa_circ_42105 5825 RMVar_ID_5825 Human_SNP_ID_515527691 A-to-I Human chr12 - 109970914 109970914 109970914 GTGATGGTGCATGCCTGTGGTCTCACCTACTCAGGAGGCTGATGTGGGAAGATCACCTGAGCCCA GTGATGGTGCATGCCTGTGGTCTCACCTACTCGGGAGGCTGATGTGGGAAGATCACCTGAGCCCA T C GIT2 Ensembl:ENSG00000139436 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1430691166 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6072,RMVar_hsa_circ_119788,RMVar_hsa_circ_159740,RMVar_hsa_circ_159745,RMVar_hsa_circ_30936,RMVar_hsa_circ_83049,RMVar_hsa_circ_159747,RMVar_hsa_circ_66797,RMVar_hsa_circ_71444,RMVar_hsa_circ_94773,RMVar_hsa_circ_21638,RMVar_hsa_circ_102178,RMVar_hsa_circ_82793,RMVar_hsa_circ_159750,RMVar_hsa_circ_159751,RMVar_hsa_circ_159752,RMVar_hsa_circ_62471,RMVar_hsa_circ_159753,RMVar_hsa_circ_278122,RMVar_hsa_circ_336994 5826 RMVar_ID_5826 Human_SNP_ID_515530888 A-to-I Human chr12 - 109984603 109984603 109984603 ATCTGTATTGAAAAATAAAAAGTTAGCAGGGCATGGTGGCCGGCGCCTGTAGTCCCAGCTGTTTG ATCTGTATTGAAAAATAAAAAGTTAGCAGGGCGTGGTGGCCGGCGCCTGTAGTCCCAGCTGTTTG T C GIT2 Ensembl:ENSG00000139436 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1312091039 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6072,RMVar_hsa_circ_159745,RMVar_hsa_circ_30936,RMVar_hsa_circ_71444,RMVar_hsa_circ_94773,RMVar_hsa_circ_82793,RMVar_hsa_circ_159750,RMVar_hsa_circ_159751,RMVar_hsa_circ_52431,RMVar_hsa_circ_90810,RMVar_hsa_circ_159753,RMVar_hsa_circ_278122,RMVar_hsa_circ_336994,RMVar_hsa_circ_284875,RMVar_hsa_circ_34251,RMVar_hsa_circ_159755,RMVar_hsa_circ_159756,RMVar_hsa_circ_55687,RMVar_hsa_circ_69661 5827 RMVar_ID_5827 Human_SNP_ID_515530891 A-to-I Human chr12 - 109984619 109984619 109984619 AACATAGTGAGACCTCATCTGTATTGAAAAATAAAAAGTTAGCAGGGCATGGTGGCCGGCGCCTG AACATAGTGAGACCTCATCTGTATTGAAAAATTAAAAGTTAGCAGGGCATGGTGGCCGGCGCCTG T A GIT2 Ensembl:ENSG00000139436 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1221293099 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6072,RMVar_hsa_circ_159745,RMVar_hsa_circ_30936,RMVar_hsa_circ_71444,RMVar_hsa_circ_94773,RMVar_hsa_circ_82793,RMVar_hsa_circ_159750,RMVar_hsa_circ_159751,RMVar_hsa_circ_52431,RMVar_hsa_circ_90810,RMVar_hsa_circ_159753,RMVar_hsa_circ_278122,RMVar_hsa_circ_336994,RMVar_hsa_circ_284875,RMVar_hsa_circ_34251,RMVar_hsa_circ_159755,RMVar_hsa_circ_159756,RMVar_hsa_circ_55687,RMVar_hsa_circ_69661 5828 RMVar_ID_5828 Human_SNP_ID_515531601 A-to-I Human chr12 - 109987569 109987569 109987569 CCAGCTACCTGGGAGGCTGAGGTTGGAGGATGACTTGAGCCCAGGAGGTGGAGGTTGCAGTGAGC CCAGCTACCTGGGAGGCTGAGGTTGGAGGATGGCTTGAGCCCAGGAGGTGGAGGTTGCAGTGAGC T C GIT2 Ensembl:ENSG00000139436 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1472504817 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6072,RMVar_hsa_circ_159745,RMVar_hsa_circ_30936,RMVar_hsa_circ_71444,RMVar_hsa_circ_94773,RMVar_hsa_circ_82793,RMVar_hsa_circ_159750,RMVar_hsa_circ_159751,RMVar_hsa_circ_52431,RMVar_hsa_circ_90810,RMVar_hsa_circ_159753,RMVar_hsa_circ_278122,RMVar_hsa_circ_336994,RMVar_hsa_circ_284875,RMVar_hsa_circ_34251,RMVar_hsa_circ_159755,RMVar_hsa_circ_159756,RMVar_hsa_circ_55687,RMVar_hsa_circ_69661 5829 RMVar_ID_5829 Human_SNP_ID_532676308 A-to-I Human chr13 - 60040051 60040051 60040051 TTTGTATTTTTAGTAGAGACAGGCCTCACCATATTGGCCAGGCTGGTCTTGAATTCCTGACCTCT TTTGTATTTTTAGTAGAGACAGGCCTCACCATGTTGGCCAGGCTGGTCTTGAATTCCTGACCTCT T C DIAPH3 Ensembl:ENSG00000139734 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs547324261 Functional Loss SNV dbSNP153 33..33 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 5830 RMVar_ID_5830 Human_SNP_ID_534345525 A-to-I Human chr13 - 66539994 66539994 66539994 ATAGTGGTTCAGGCCTGTAATCTCAGCTACTCAGGAGGCTAAGGTAGGAGCATGGCTTGAGCCCA ATAGTGGTTCAGGCCTGTAATCTCAGCTACTCCGGAGGCTAAGGTAGGAGCATGGCTTGAGCCCA T G PCDH9 Ensembl:ENSG00000184226 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 29129909,30559470 RNA-Seq:(High) rs938820603 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9033897 RMVar_hsa_circ_96620,RMVar_hsa_circ_163640 5831 RMVar_ID_5831 Human_SNP_ID_534345565 A-to-I Human chr13 - 66540163 66540163 66540163 AGTCATTAATATTCTAAACTTTGCCAGGAACAATGGCTCACACTTGTAATCCCAGCACTTTGGCA AGTCATTAATATTCTAAACTTTGCCAGGAACAGTGGCTCACACTTGTAATCCCAGCACTTTGGCA T C PCDH9 Ensembl:ENSG00000184226 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1346410891 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96620,RMVar_hsa_circ_163640 5832 RMVar_ID_5832 Human_SNP_ID_534349767 A-to-I Human chr13 - 66557948 66557948 66557948 GGGTCTCTCCATGTTGCCCACACTGGTCTCCAAACTCCTGGCCTGAAGCGATCCTCCAGTCTTGG GGGTCTCTCCATGTTGCCCACACTGGTCTCCATACTCCTGGCCTGAAGCGATCCTCCAGTCTTGG T A PCDH9 Ensembl:ENSG00000184226 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1566414906 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96620,RMVar_hsa_circ_163640 5833 RMVar_ID_5833 Human_SNP_ID_534351596 A-to-I Human chr13 - 66564415 66564415 66564415 ATGCCTGTAATCCTAGCACTTTGAGAGGTCAAAGGGAGAGAATCATTTGAGCCCAGGAGTTCAAG ATGCCTGTAATCCTAGCACTTTGAGAGGTCAACGGGAGAGAATCATTTGAGCCCAGGAGTTCAAG T G PCDH9 Ensembl:ENSG00000184226 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1226136730 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96620,RMVar_hsa_circ_163640 5834 RMVar_ID_5834 Human_SNP_ID_534355419 A-to-I Human chr13 - 66580510 66580510 66580510 CATTGACAAATACTCCCACACTACCCCACTCCATATTTCTTAGCATTTGACAATATTAGGCACTT CATTGACAAATACTCCCACACTACCCCACTCCCTATTTCTTAGCATTTGACAATATTAGGCACTT T G PCDH9 Ensembl:ENSG00000184226 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1015022684 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96620,RMVar_hsa_circ_163640 5835 RMVar_ID_5835 Human_SNP_ID_534355428 A-to-I Human chr13 - 66580544 66580544 66580544 CAACAGTTTTATCACCCCAGAAAGATGTCCATACCATTGACAAATACTCCCACACTACCCCACTC CAACAGTTTTATCACCCCAGAAAGATGTCCATCCCATTGACAAATACTCCCACACTACCCCACTC T G PCDH9 Ensembl:ENSG00000184226 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1023108611 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96620,RMVar_hsa_circ_163640 5836 RMVar_ID_5836 Human_SNP_ID_534356539 A-to-I Human chr13 - 66585207 66585207 66585207 ATAAAAATTCTCTTCAGAAAAATAATGCATATATGCATTTAATAAAATAAATAAATGCATGCACC ATAAAAATTCTCTTCAGAAAAATAATGCATATGTGCATTTAATAAAATAAATAAATGCATGCACC T C PCDH9 Ensembl:ENSG00000184226 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs958155271 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96620,RMVar_hsa_circ_163640 5837 RMVar_ID_5837 Human_SNP_ID_534356540 A-to-I Human chr13 - 66585207 66585207 66585207 ATAAAAATTCTCTTCAGAAAAATAATGCATATATGCATTTAATAAAATAAATAAATGCATGCACC ATAAAAATTCTCTTCAGAAAAATAATGCATATCTGCATTTAATAAAATAAATAAATGCATGCACC T G PCDH9 Ensembl:ENSG00000184226 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs958155271 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96620,RMVar_hsa_circ_163640 5838 RMVar_ID_5838 Human_SNP_ID_534390874 A-to-I Human chr13 - 66727211 66727211 66727211 TGTCATCCTGGCTGGTGTGCAGTGGCATGATCATAGCTCACTGCAGCCTTGGACTGGGCTCAGGG TGTCATCCTGGCTGGTGTGCAGTGGCATGATCCTAGCTCACTGCAGCCTTGGACTGGGCTCAGGG T G PCDH9 Ensembl:ENSG00000184226 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1201205658 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96620,RMVar_hsa_circ_163640,RMVar_hsa_circ_45969 5839 RMVar_ID_5839 Human_SNP_ID_534416198 A-to-I Human chr13 - 66824572 66824572 66824572 GGGCTGACTGCAACATCTGTCTCCTGGGTTCAAGCAATTCTCCTGCCTCAGCCTACCGGGTAGCT GGGCTGACTGCAACATCTGTCTCCTGGGTTCACGCAATTCTCCTGCCTCAGCCTACCGGGTAGCT T G PCDH9 Ensembl:ENSG00000184226 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs923693662 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96620,RMVar_hsa_circ_163640,RMVar_hsa_circ_45969 5840 RMVar_ID_5840 Human_SNP_ID_534418767 A-to-I Human chr13 - 66834414 66834414 66834414 TCAGGGGCTGGGAGTGGTGGCTCATGACTGTAATCCAAGCACTCTGGGAGGCCGAGGCGGGTGGA TCAGGGGCTGGGAGTGGTGGCTCATGACTGTAGTCCAAGCACTCTGGGAGGCCGAGGCGGGTGGA T C PCDH9 Ensembl:ENSG00000184226 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1293102467 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96620,RMVar_hsa_circ_163640,RMVar_hsa_circ_45969 5841 RMVar_ID_5841 Human_SNP_ID_534426631 A-to-I Human chr13 - 66866685 66866685 66866685 TCAAGTGATTCTTCTGCCTCAGCTTCCTGAGTAGCTGGGACTATAGGCGCTCGCCACCACGGCCG TCAAGTGATTCTTCTGCCTCAGCTTCCTGAGTGGCTGGGACTATAGGCGCTCGCCACCACGGCCG T C PCDH9 Ensembl:ENSG00000184226 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs536227462 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_163645,RMVar_hsa_circ_96620,RMVar_hsa_circ_163640,RMVar_hsa_circ_45969 5842 RMVar_ID_5842 Human_SNP_ID_534444439 A-to-I Human chr13 - 66939645 66939645 66939645 GGGAGGCTGAGGTGGGTGGATCACTTGAGGTCAGGAGTTCAAGACCAGCCGTGTCTCTACTAAAA GGGAGGCTGAGGTGGGTGGATCACTTGAGGTCGGGAGTTCAAGACCAGCCGTGTCTCTACTAAAA T C PCDH9 Ensembl:ENSG00000184226 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs968586924 Functional Loss SNV dbSNP153 33..33 33 - - - 5843 RMVar_ID_5843 Human_SNP_ID_534448021 A-to-I Human chr13 - 66954849 66954849 66954849 TGAGGCAGGAGAATGGCGTGAACCTGGGAGGCAGAGTTTTCAGTGAGCTGAGATCACGCCACTGC TGAGGCAGGAGAATGGCGTGAACCTGGGAGGCGGAGTTTTCAGTGAGCTGAGATCACGCCACTGC T C PCDH9 Ensembl:ENSG00000184226 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1354589192 Functional Loss SNV dbSNP153 33..33 33 - - - 5844 RMVar_ID_5844 Human_SNP_ID_534453260 A-to-I Human chr13 - 66977781 66977781 66977781 AGAAGCACCATTTCCCAGCACTCTTTTCTGGTAGAAGCTGGGTTCCTGGTGGAAATGATGCTGCT AGAAGCACCATTTCCCAGCACTCTTTTCTGGTGGAAGCTGGGTTCCTGGTGGAAATGATGCTGCT T C PCDH9 Ensembl:ENSG00000184226 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1179387606 Functional Loss SNV dbSNP153 33..33 33 - - - 5845 RMVar_ID_5845 Human_SNP_ID_534455434 A-to-I Human chr13 - 66986112 66986112 66986112 GTGAAGAAGACATGTTTGCTTCCCCTTCCACCATGATTATAAGTTTCCTGAGGCCTCCCCAGCCA GTGAAGAAGACATGTTTGCTTCCCCTTCCACCGTGATTATAAGTTTCCTGAGGCCTCCCCAGCCA T C PCDH9 Ensembl:ENSG00000184226 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1461587290 Functional Loss SNV dbSNP153 33..33 33 - - - 5846 RMVar_ID_5846 Human_SNP_ID_534463028 A-to-I Human chr13 - 67018462 67018462 67018462 GGCAGACGCCACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACTATGTTGA GGCAGACGCCACCACGCCCAGCTAATTTTTGTGTTTTTAGTAGAGACGGGGTTTCACTATGTTGA T C PCDH9 Ensembl:ENSG00000184226 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1257688518 Functional Loss SNV dbSNP153 33..33 33 - - - 5847 RMVar_ID_5847 Human_SNP_ID_534463029 A-to-I Human chr13 - 67018471 67018471 67018471 GGGACTACAGGCAGACGCCACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCA GGGACTACAGGCAGACGCCACCACGCCCAGCTGATTTTTGTATTTTTAGTAGAGACGGGGTTTCA T C PCDH9 Ensembl:ENSG00000184226 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1193627343 Functional Loss SNV dbSNP153 33..33 33 - - - 5848 RMVar_ID_5848 Human_SNP_ID_534466491 A-to-I Human chr13 - 67032251 67032251 67032251 TAGTCCCAGCTACTTGCGAGGTTGAGGTGGGAAGATGGCTTGAGCCCGGGAAGTGTAGGCTACAG TAGTCCCAGCTACTTGCGAGGTTGAGGTGGGAGGATGGCTTGAGCCCGGGAAGTGTAGGCTACAG T C PCDH9 Ensembl:ENSG00000184226 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1041901430 Functional Loss SNV dbSNP153 33..33 33 - - - 5849 RMVar_ID_5849 Human_SNP_ID_534466492 A-to-I Human chr13 - 67032251 67032251 67032251 TAGTCCCAGCTACTTGCGAGGTTGAGGTGGGAAGATGGCTTGAGCCCGGGAAGTGTAGGCTACAG TAGTCCCAGCTACTTGCGAGGTTGAGGTGGGACGATGGCTTGAGCCCGGGAAGTGTAGGCTACAG T G PCDH9 Ensembl:ENSG00000184226 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1041901430 Functional Loss SNV dbSNP153 33..33 33 - - - 5850 RMVar_ID_5850 Human_SNP_ID_534471019 A-to-I Human chr13 - 67051530 67051530 67051530 AAATTAGCTGGGCGTGGTGGCACGCACCTGTAATCCCAGCTATTCGGGAGGCTGAGGCAGGAGAA AAATTAGCTGGGCGTGGTGGCACGCACCTGTAGTCCCAGCTATTCGGGAGGCTGAGGCAGGAGAA T C PCDH9 Ensembl:ENSG00000184226 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs550056991 Functional Loss SNV dbSNP153 33..33 33 - - - 5851 RMVar_ID_5851 Human_SNP_ID_534485285 A-to-I Human chr13 - 67112821 67112821 67112821 CCAGCTACTCGGGAAGCTGAGGTGTGAGGATCACTGGAGCCTTGGGAGGTCGAGGCTGCAGTTAA CCAGCTACTCGGGAAGCTGAGGTGTGAGGATCTCTGGAGCCTTGGGAGGTCGAGGCTGCAGTTAA T A PCDH9 Ensembl:ENSG00000184226 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs559232356 Functional Loss SNV dbSNP153 33..33 33 - - - 5852 RMVar_ID_5852 Human_SNP_ID_534485286 A-to-I Human chr13 - 67112821 67112821 67112821 CCAGCTACTCGGGAAGCTGAGGTGTGAGGATCACTGGAGCCTTGGGAGGTCGAGGCTGCAGTTAA CCAGCTACTCGGGAAGCTGAGGTGTGAGGATCGCTGGAGCCTTGGGAGGTCGAGGCTGCAGTTAA T C PCDH9 Ensembl:ENSG00000184226 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs559232356 Functional Loss SNV dbSNP153 33..33 33 - - - 5853 RMVar_ID_5853 Human_SNP_ID_534491901 A-to-I Human chr13 - 67141405 67141405 67141405 TAAAGAGAGAGAGAGAGAGAGAAGATCTTACTATATTGCCCAGGCTGGTCTTGAACTCCTGGGGT TAAAGAGAGAGAGAGAGAGAGAAGATCTTACTGTATTGCCCAGGCTGGTCTTGAACTCCTGGGGT T C PCDH9 Ensembl:ENSG00000184226 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1247531016 Functional Loss SNV dbSNP153 33..33 33 - - - 5854 RMVar_ID_5854 Human_SNP_ID_534495232 A-to-I Human chr13 - 67154848 67154848 67154848 ATACAAAAAATTTGCTGGGTGTGGTGACACGCACCTGTAGTACCAGCTACTAGGGAGGCTGAGGC ATACAAAAAATTTGCTGGGTGTGGTGACACGCGCCTGTAGTACCAGCTACTAGGGAGGCTGAGGC T C PCDH9 Ensembl:ENSG00000184226 Protein coding intron GSE107867 ASD brains,cerebellum;ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs533805459 Functional Loss SNV dbSNP153 33..33 33 - - - 5855 RMVar_ID_5855 Human_SNP_ID_534497009 A-to-I Human chr13 - 67162039 67162039 67162039 CCCAGAAGATAGAGCAAAAAACTCTACTTCCAAGGTCGTTTAGGAAGGCGGACTTGAACAAAACA CCCAGAAGATAGAGCAAAAAACTCTACTTCCAGGGTCGTTTAGGAAGGCGGACTTGAACAAAACA T C PCDH9 Ensembl:ENSG00000184226 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs547387641 Functional Loss SNV dbSNP153 33..33 33 - - - 5856 RMVar_ID_5856 Human_SNP_ID_534499124 A-to-I Human chr13 - 67170803 67170803 67170803 CTTGTGCCTCAGCCTCCCGAGTAGATGGGATTACAGGAGTGCACCACCAGGCCCAGCTAATTTTT CTTGTGCCTCAGCCTCCCGAGTAGATGGGATTGCAGGAGTGCACCACCAGGCCCAGCTAATTTTT T C PCDH9 Ensembl:ENSG00000184226 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs975673663 Functional Loss SNV dbSNP153 33..33 33 - - - 5857 RMVar_ID_5857 Human_SNP_ID_534502512 A-to-I Human chr13 - 67184469 67184469 67184469 CCGCCTTAGCCTCCCAGAGTTCTGTGATTACAAGCATGAGTCACCATGCCTGGGCCCTACCCTTA CCGCCTTAGCCTCCCAGAGTTCTGTGATTACAGGCATGAGTCACCATGCCTGGGCCCTACCCTTA T C PCDH9 Ensembl:ENSG00000184226 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs986586301 Functional Loss SNV dbSNP153 33..33 33 - - - 5858 RMVar_ID_5858 Human_SNP_ID_534502602 A-to-I Human chr13 - 67184717 67184717 67184717 TTGTTTGTTGGTTGGTTTTTAGACAGGGTCTCACTTTTTCACCCAGGCTGGAATGCAGTGGTGCG TTGTTTGTTGGTTGGTTTTTAGACAGGGTCTCCCTTTTTCACCCAGGCTGGAATGCAGTGGTGCG T G PCDH9 Ensembl:ENSG00000184226 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs938651920 Functional Loss SNV dbSNP153 33..33 33 - - - 5859 RMVar_ID_5859 Human_SNP_ID_535911163 A-to-I Human chr13 + 72732637 72732637 72732637 AGGCAAAGGTTGCAGTGAGCTGAGATCATGCCATTGCACTCTAGCCTGGGGGACAGAGCAAGACT AGGCAAAGGTTGCAGTGAGCTGAGATCATGCCCTTGCACTCTAGCCTGGGGGACAGAGCAAGACT A C BORA Ensembl:ENSG00000136122 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965976331 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9741798,Human_RBP_ID_25080062 RMVar_hsa_circ_58769,RMVar_hsa_circ_41622,RMVar_hsa_circ_115217,RMVar_hsa_circ_277681,RMVar_hsa_circ_341171,RMVar_hsa_circ_61438,RMVar_hsa_circ_163687,RMVar_hsa_circ_163688 5860 RMVar_ID_5860 Human_SNP_ID_535923278 A-to-I Human chr13 - 72780269 72780269 72780269 CAGGCTGGAGTGCAGTGGTGTGATCTCTGCTCACTGCAACCTCCACCTCCCAAGTTCAAGCGATT CAGGCTGGAGTGCAGTGGTGTGATCTCTGCTCGCTGCAACCTCCACCTCCCAAGTTCAAGCGATT T C DIS3 Ensembl:ENSG00000083520 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs919986746 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42945,RMVar_hsa_circ_70087,RMVar_hsa_circ_355305,RMVar_hsa_circ_108474,RMVar_hsa_circ_163696 5861 RMVar_ID_5861 Human_SNP_ID_535959241 A-to-I Human chr13 + 72920666 72920666 72920666 GATTGGAGCCAGACGCACTGGCATGTACCTGTAATCCCAGCTTCTGGGGAGCCTGAGGCAGAAGG GATTGGAGCCAGACGCACTGGCATGTACCTGTCATCCCAGCTTCTGGGGAGCCTGAGGCAGAAGG A C PIBF1 Ensembl:ENSG00000083535 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1448857851 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_163699,RMVar_hsa_circ_372291,RMVar_hsa_circ_117928,RMVar_hsa_circ_163700,RMVar_hsa_circ_70924,RMVar_hsa_circ_69026,RMVar_hsa_circ_370151,RMVar_hsa_circ_163703,RMVar_hsa_circ_288184,RMVar_hsa_circ_9812,RMVar_hsa_circ_47180,RMVar_hsa_circ_284214,RMVar_hsa_circ_331032,RMVar_hsa_circ_163713,RMVar_hsa_circ_163714,RMVar_hsa_circ_63778,RMVar_hsa_circ_312958,RMVar_hsa_circ_163716,RMVar_hsa_circ_341264,RMVar_hsa_circ_163715,RMVar_hsa_circ_314046,RMVar_hsa_circ_163717,RMVar_hsa_circ_316159,RMVar_hsa_circ_350899,RMVar_hsa_circ_351068,RMVar_hsa_circ_163718,RMVar_hsa_circ_163719,RMVar_hsa_circ_329957,RMVar_hsa_circ_342258,RMVar_hsa_circ_319332,RMVar_hsa_circ_163723,RMVar_hsa_circ_163725,RMVar_hsa_circ_163724,RMVar_hsa_circ_163721,RMVar_hsa_circ_163722,RMVar_hsa_circ_328386,RMVar_hsa_circ_163720,RMVar_hsa_circ_276845,RMVar_hsa_circ_163727,RMVar_hsa_circ_163728,RMVar_hsa_circ_163729,RMVar_hsa_circ_163726 5862 RMVar_ID_5862 Human_SNP_ID_535962349 A-to-I Human chr13 + 72932107 72932107 72932107 GGAACTGTAGCTACGCACTACTGTGCCTGGCTAATTTTTGTATTTTTTTGGTAGAGACAGGGTTT GGAACTGTAGCTACGCACTACTGTGCCTGGCTGATTTTTGTATTTTTTTGGTAGAGACAGGGTTT A G PIBF1 Ensembl:ENSG00000083535 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025048972 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117928,RMVar_hsa_circ_163700,RMVar_hsa_circ_70924,RMVar_hsa_circ_370151,RMVar_hsa_circ_163703,RMVar_hsa_circ_9812,RMVar_hsa_circ_47180,RMVar_hsa_circ_331032,RMVar_hsa_circ_163714,RMVar_hsa_circ_312958,RMVar_hsa_circ_341264,RMVar_hsa_circ_163715,RMVar_hsa_circ_163717,RMVar_hsa_circ_350899,RMVar_hsa_circ_351068,RMVar_hsa_circ_163719,RMVar_hsa_circ_329957,RMVar_hsa_circ_342258,RMVar_hsa_circ_163723,RMVar_hsa_circ_163725,RMVar_hsa_circ_163724,RMVar_hsa_circ_163721,RMVar_hsa_circ_163722,RMVar_hsa_circ_328386,RMVar_hsa_circ_58451,RMVar_hsa_circ_163727,RMVar_hsa_circ_163728,RMVar_hsa_circ_163726,RMVar_hsa_circ_163731,RMVar_hsa_circ_30104,RMVar_hsa_circ_163730 5863 RMVar_ID_5863 Human_SNP_ID_535971300 A-to-I Human chr13 + 72968934 72968934 72968934 GTGATGGCACGCTTCTGTAGTCCTGGCTACTCAGGAGGCTGAGGTGGGAGGATGAGTTGAGCCTG GTGATGGCACGCTTCTGTAGTCCTGGCTACTCCGGAGGCTGAGGTGGGAGGATGAGTTGAGCCTG A C PIBF1 Ensembl:ENSG00000083535 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270461711 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117928,RMVar_hsa_circ_163700,RMVar_hsa_circ_70924,RMVar_hsa_circ_370151,RMVar_hsa_circ_163703,RMVar_hsa_circ_163732,RMVar_hsa_circ_47180,RMVar_hsa_circ_331032,RMVar_hsa_circ_312958,RMVar_hsa_circ_341264,RMVar_hsa_circ_350899,RMVar_hsa_circ_329957,RMVar_hsa_circ_163725,RMVar_hsa_circ_163724,RMVar_hsa_circ_328386,RMVar_hsa_circ_163726,RMVar_hsa_circ_163731,RMVar_hsa_circ_30104,RMVar_hsa_circ_163734,RMVar_hsa_circ_276701,RMVar_hsa_circ_295137,RMVar_hsa_circ_163733 5864 RMVar_ID_5864 Human_SNP_ID_535987399 A-to-I Human chr13 + 73030916 73030916 73030916 TTCCTACCTCAGCCTCCCAAAGTGCTGGGATTATAAACATGAGCCACCTCGCCTGTCCTCATATC TTCCTACCTCAGCCTCCCAAAGTGCTGGGATTGTAAACATGAGCCACCTCGCCTGTCCTCATATC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1224639089 Functional Loss SNV dbSNP153 33..33 33 - - - 5865 RMVar_ID_5865 Human_SNP_ID_535997594 A-to-I Human chr13 + 73068973 73068973 73068973 CAAAAATTAGCTGGGCATGGTGGCACATGCCTATAGTCCCAGCTACTTGGGAGCCTGATGCAGGA CAAAAATTAGCTGGGCATGGTGGCACATGCCTGTAGTCCCAGCTACTTGGGAGCCTGATGCAGGA A G KLF5 Ensembl:ENSG00000102554 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs990426163 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2389939 RMVar_hsa_circ_117961,RMVar_hsa_circ_163735 5866 RMVar_ID_5866 Human_SNP_ID_535997599 A-to-I Human chr13 + 73069007 73069007 73069007 AGTCCCAGCTACTTGGGAGCCTGATGCAGGAGAATTGCTTGAACCTGGGAGGCAGAGGTTGTGGT AGTCCCAGCTACTTGGGAGCCTGATGCAGGAGCATTGCTTGAACCTGGGAGGCAGAGGTTGTGGT A C KLF5 Ensembl:ENSG00000102554 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256663036 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117961,RMVar_hsa_circ_163735 5867 RMVar_ID_5867 Human_SNP_ID_729949016 A-to-I Human chrX - 120437941 120437941 120437941 TGAGGCAGGAGAATCACTTGAACCCGGGAGGCAGAGGTTGCGGTGAGCCAAGAGCGCACCATTGC TGAGGCAGGAGAATCACTTGAACCCGGGAGGCGGAGGTTGCGGTGAGCCAAGAGCGCACCATTGC T C LAMP2 Ensembl:ENSG00000005893 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1168063141 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_726958,Human_RBP_ID_5050363,Human_RBP_ID_24326161 RMVar_hsa_circ_91824,RMVar_hsa_circ_263681 5868 RMVar_ID_5868 Human_SNP_ID_729967749 A-to-I Human chrX - 120547573 120547573 120547573 CTCTCACCTTGGCCCCCCAAAATGTTGGGATTACAGGCATGAACCACTGTACCCAGCCCAAGTAG CTCTCACCTTGGCCCCCCAAAATGTTGGGATTGCAGGCATGAACCACTGTACCCAGCCCAAGTAG T C CUL4B Ensembl:ENSG00000158290 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs921757285 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21311,RMVar_hsa_circ_36168,RMVar_hsa_circ_50585,RMVar_hsa_circ_9166,RMVar_hsa_circ_19921 5869 RMVar_ID_5869 Human_SNP_ID_729978494 A-to-I Human chrX + 120610303 120610291 120610304 GAGATCATGCCACTGCACTCCAGCCGGGTGACAAAGCAAGACTCCATCTCAAAAAAACAAACGGC GAGATCATGCCACTGCACTCC_____________AGCAAGACTCCATCTCAAAAAAACAAACGGC CAGCCGGGTGACAA C MCTS1 Ensembl:ENSG00000232119 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1395155446 Functional Loss DEL dbSNP153 22..34 33 - - - RMVar_hsa_circ_19404,RMVar_hsa_circ_53548,RMVar_hsa_circ_263693 5870 RMVar_ID_5870 Human_SNP_ID_729979971 A-to-I Human chrX + 120620265 120620265 120620265 GGGAGGCGGAGCTTGCAGTGAGCTGAGATCGCACCACTGCATTCCAGCCTGGACAACAGAGCGAA GGGAGGCGGAGCTTGCAGTGAGCTGAGATCGCGCCACTGCATTCCAGCCTGGACAACAGAGCGAA A G MCTS1 Ensembl:ENSG00000232119 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965143681 Functional Loss SNV dbSNP153 33..33 33 - - - 5871 RMVar_ID_5871 Human_SNP_ID_729980253 A-to-I Human chrX - 120621481 120621481 120621481 CATATTCTTTCTTTCTTTTGAGATGGAGTCTCACTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCA CATATTCTTTCTTTCTTTTGAGATGGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCA T C lnc-C1GALT1C1-1 RNACentral:URS00008B403B lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1164203943 Functional Loss SNV dbSNP153 33..33 33 - - - 5872 RMVar_ID_5872 Human_SNP_ID_730034976 A-to-I Human chrX + 121048582 121048582 121048582 ACATGAGCATTTTAGGAATGACACCAGGGTTTAGAGATAAAACATTTGTTGTTCAGGGATTTGGT ACATGAGCATTTTAGGAATGACACCAGGGTTTGGAGATAAAACATTTGTTGTTCAGGGATTTGGT A G GLUD2 Ensembl:ENSG00000182890 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs776965882 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 5873 RMVar_ID_5873 Human_SNP_ID_730035112 A-to-I Human chrX + 121049252 121049252 121049252 CACAATGGAGCGTTCTGCCAGGCAAATTATGCACACAGCCATGAAGTATAACCTGGGATTGGACC CACAATGGAGCGTTCTGCCAGGCAAATTATGCGCACAGCCATGAAGTATAACCTGGGATTGGACC A G GLUD2 Ensembl:ENSG00000182890 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs778620218 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 5874 RMVar_ID_5874 Human_SNP_ID_730501071 A-to-I Human chrX - 123608279 123608279 123608279 CTCCTGCCTCACCCTCCCTAGTAGTTGGGACTACAAGCACGTGCCACCACGCCTGGCTAATTTTT CTCCTGCCTCACCCTCCCTAGTAGTTGGGACTGCAAGCACGTGCCACCACGCCTGGCTAATTTTT T C THOC2 Ensembl:ENSG00000125676 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1204086075 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16807459 RMVar_hsa_circ_263704 5875 RMVar_ID_5875 Human_SNP_ID_730513772 A-to-I Human chrX - 123683886 123683886 123683886 TTGTTAGAACTGTCTTATGGGCCAGGCGTGGTAGCTTACACCTGTAATTCCAGCATTTTTGGAGG TTGTTAGAACTGTCTTATGGGCCAGGCGTGGTGGCTTACACCTGTAATTCCAGCATTTTTGGAGG T C THOC2 Ensembl:ENSG00000125676 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1371055012 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21959032 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 5876 RMVar_ID_5876 Human_SNP_ID_730514853 A-to-I Human chrX - 123690994 123690994 123690994 TTGCCCTGGCAGGTCTCGAACTCCTGAGCTCAAGCTATCTACCTGCCTTGGCCTCCTAAATTGCT TTGCCCTGGCAGGTCTCGAACTCCTGAGCTCACGCTATCTACCTGCCTTGGCCTCCTAAATTGCT T G THOC2 Ensembl:ENSG00000125676 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1323633522 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16809594,Human_RBP_ID_26302817 RMVar_hsa_circ_5358,RMVar_hsa_circ_53709,RMVar_hsa_circ_57239,RMVar_hsa_circ_21392,RMVar_hsa_circ_14091,RMVar_hsa_circ_54617,RMVar_hsa_circ_43527,RMVar_hsa_circ_32078,RMVar_hsa_circ_42837,RMVar_hsa_circ_297130,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_311158,RMVar_hsa_circ_286032,RMVar_hsa_circ_288342,RMVar_hsa_circ_320937,RMVar_hsa_circ_73439,RMVar_hsa_circ_263720,RMVar_hsa_circ_263721,RMVar_hsa_circ_263719 5877 RMVar_ID_5877 Human_SNP_ID_730548816 A-to-I Human chrX + 123862330 123862330 123862330 ACCTCAGGTGATGCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTAAAGGTATGAGCCACCTCGC ACCTCAGGTGATGCACCCGCCTCGGCCTCCCAGAGTGCTGGGATTAAAGGTATGAGCCACCTCGC A G XIAP Ensembl:ENSG00000101966 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984753491 Functional Loss SNV dbSNP153 33..33 33 - - - 5878 RMVar_ID_5878 Human_SNP_ID_730548866 A-to-I Human chrX + 123862605 123862605 123862605 ATTTGACACCTGACGCTGTGGCTCATGTCTGTAATCCCAGCACTTTGGGACGCCAAGGCGGGCAG ATTTGACACCTGACGCTGTGGCTCATGTCTGTGATCCCAGCACTTTGGGACGCCAAGGCGGGCAG A G XIAP Ensembl:ENSG00000101966 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1200917454 Functional Loss SNV dbSNP153 33..33 33 - - - 5879 RMVar_ID_5879 Human_SNP_ID_730548911 A-to-I Human chrX + 123862812 123862812 123862812 AGGAGGCAGAGGCTGCAGTGAGCCGAGATTGCACCACTGTACTCCAGCCTGGGTGACAACAGTGC AGGAGGCAGAGGCTGCAGTGAGCCGAGATTGCGCCACTGTACTCCAGCCTGGGTGACAACAGTGC A G XIAP Ensembl:ENSG00000101966 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1177220962 Functional Loss SNV dbSNP153 33..33 33 - - - 5880 RMVar_ID_5880 Human_SNP_ID_730549061 A-to-I Human chrX + 123863626 123863626 123863626 CTGCCTCCCAGGTTCAAGCAGTTTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCATGCG CTGCCTCCCAGGTTCAAGCAGTTTCCTGCCTCGGCCTCCCGAGTAGCTGGGATTACAGGCATGCG A G XIAP Ensembl:ENSG00000101966 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1399473797 Functional Loss SNV dbSNP153 33..33 33 - - - 5881 RMVar_ID_5881 Human_SNP_ID_730549062 A-to-I Human chrX + 123863626 123863626 123863626 CTGCCTCCCAGGTTCAAGCAGTTTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCATGCG CTGCCTCCCAGGTTCAAGCAGTTTCCTGCCTCTGCCTCCCGAGTAGCTGGGATTACAGGCATGCG A T XIAP Ensembl:ENSG00000101966 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1399473797 Functional Loss SNV dbSNP153 33..33 33 - - - 5882 RMVar_ID_5882 Human_SNP_ID_730550554 A-to-I Human chrX + 123869444 123869444 123869444 TACTTAGGAGGCTGAGGCAGGAAAATTACTTGAGCCTGGGAGGTGGAGGTTGCAGTGAGCTGAGA TACTTAGGAGGCTGAGGCAGGAAAATTACTTGCGCCTGGGAGGTGGAGGTTGCAGTGAGCTGAGA A C XIAP Ensembl:ENSG00000101966 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1452920375 Functional Loss SNV dbSNP153 33..33 33 - - - 5883 RMVar_ID_5883 Human_SNP_ID_730551036 A-to-I Human chrX + 123872026 123872026 123872026 TGGAGGCTAAGGCACGAGAATTGCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCCGAGATTGTG TGGAGGCTAAGGCACGAGAATTGCTTGAACCCGGGAGGCGGAGGTTGCAGTGAGCCGAGATTGTG A G XIAP Ensembl:ENSG00000101966 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1284690775 Functional Loss SNV dbSNP153 33..33 33 - - - 5884 RMVar_ID_5884 Human_SNP_ID_730551037 A-to-I Human chrX + 123872026 123872026 123872026 TGGAGGCTAAGGCACGAGAATTGCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCCGAGATTGTG TGGAGGCTAAGGCACGAGAATTGCTTGAACCCTGGAGGCGGAGGTTGCAGTGAGCCGAGATTGTG A T XIAP Ensembl:ENSG00000101966 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1284690775 Functional Loss SNV dbSNP153 33..33 33 - - - 5885 RMVar_ID_5885 Human_SNP_ID_730551935 A-to-I Human chrX + 123876446 123876446 123876446 AAAAAACTAGTCAAACACAGTGGTTCACGCCTATAATCACAACACTTTGGGAGGCCAAGTCAGGA AAAAAACTAGTCAAACACAGTGGTTCACGCCTGTAATCACAACACTTTGGGAGGCCAAGTCAGGA A G XIAP Ensembl:ENSG00000101966 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs761379578 Functional Loss SNV dbSNP153 33..33 33 - - - 5886 RMVar_ID_5886 Human_SNP_ID_730551943 A-to-I Human chrX + 123876494 123876494 123876494 GGGAGGCCAAGTCAGGAGTATAGCTTGAGTCCAGGAATTCCAGACCAGCCTGTACAGCATAGAGA GGGAGGCCAAGTCAGGAGTATAGCTTGAGTCCGGGAATTCCAGACCAGCCTGTACAGCATAGAGA A G XIAP Ensembl:ENSG00000101966 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1366964246 Functional Loss SNV dbSNP153 33..33 33 - - - 5887 RMVar_ID_5887 Human_SNP_ID_730551949 A-to-I Human chrX + 123876522 123876522 123876522 GTCCAGGAATTCCAGACCAGCCTGTACAGCATAGAGAAACCACATCTCTAAGAAAACTTTTTAAA GTCCAGGAATTCCAGACCAGCCTGTACAGCATGGAGAAACCACATCTCTAAGAAAACTTTTTAAA A G XIAP Ensembl:ENSG00000101966 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1348420205 Functional Loss SNV dbSNP153 33..33 33 - - - 5888 RMVar_ID_5888 Human_SNP_ID_730551959 A-to-I Human chrX + 123876582 123876582 123876582 TTAAAATTAGCAGGGCATGGTGGCATGTGGCTATAGTCCCAGCTACTCAGGAGGCTGAGGTGGGA TTAAAATTAGCAGGGCATGGTGGCATGTGGCTGTAGTCCCAGCTACTCAGGAGGCTGAGGTGGGA A G XIAP Ensembl:ENSG00000101966 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs555060248 Functional Loss SNV dbSNP153 33..33 33 - - - 5889 RMVar_ID_5889 Human_SNP_ID_730551974 A-to-I Human chrX + 123876675 123876675 123876675 TACAGTGAGCTATGATCACACTACTGCACTCCAACTCGGGCAACAGAGCAAGGCCTTGTCTTTTA TACAGTGAGCTATGATCACACTACTGCACTCCGACTCGGGCAACAGAGCAAGGCCTTGTCTTTTA A G XIAP Ensembl:ENSG00000101966 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1424564374 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16811168 5890 RMVar_ID_5890 Human_SNP_ID_730555482 A-to-I Human chrX + 123892994 123892994 123892994 AGGCCTGCGCCACCATGCCCGGCTAACTTTTTATATTTTTAGTAGAGACGGAGTTTTACCATATT AGGCCTGCGCCACCATGCCCGGCTAACTTTTTGTATTTTTAGTAGAGACGGAGTTTTACCATATT A G XIAP Ensembl:ENSG00000101966 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1245212966 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98508,RMVar_hsa_circ_330435,RMVar_hsa_circ_311218,RMVar_hsa_circ_263727 5891 RMVar_ID_5891 Human_SNP_ID_730557275 A-to-I Human chrX + 123901348 123901348 123901348 TCAAGGCTGCAGTGAGCCATGATCATGCCACTACACTTCGGCCTGGGCAACTGAGCAAGATCTTG TCAAGGCTGCAGTGAGCCATGATCATGCCACTGCACTTCGGCCTGGGCAACTGAGCAAGATCTTG A G XIAP Ensembl:ENSG00000101966 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs963082215 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5892 RMVar_ID_5892 Human_SNP_ID_730557756 A-to-I Human chrX + 123903832 123903832 123903832 TTAAACAGCCAGGCGTGGTGGCACACGCCTGTAGTTCCAGCTGCTTGGGAGGCTGAGGCAGGAGG TTAAACAGCCAGGCGTGGTGGCACACGCCTGTGGTTCCAGCTGCTTGGGAGGCTGAGGCAGGAGG A G XIAP Ensembl:ENSG00000101966 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053125704 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5893 RMVar_ID_5893 Human_SNP_ID_730557757 A-to-I Human chrX + 123903859 123903859 123903859 CCTGTAGTTCCAGCTGCTTGGGAGGCTGAGGCAGGAGGATTGCTTGAGACCAGGAGCTCAAGGCT CCTGTAGTTCCAGCTGCTTGGGAGGCTGAGGCGGGAGGATTGCTTGAGACCAGGAGCTCAAGGCT A G XIAP Ensembl:ENSG00000101966 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1429674820 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5894 RMVar_ID_5894 Human_SNP_ID_730558733 A-to-I Human chrX + 123909108 123909108 123909108 TGGAGTGCAGTGGAGTGATCTCTGCTCACTGCAACCTCCGCCTTCTGGGTTCAAGCGATTCTCGT TGGAGTGCAGTGGAGTGATCTCTGCTCACTGCGACCTCCGCCTTCTGGGTTCAAGCGATTCTCGT A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1387192342 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5895 RMVar_ID_5895 Human_SNP_ID_730558753 A-to-I Human chrX + 123909168 123909168 123909168 CTCGTGCCTCAGCTTCCTGAGTAGCTGGAATTACAGGCAGGTGCCACCATGCCCGACTAATTTTT CTCGTGCCTCAGCTTCCTGAGTAGCTGGAATTGCAGGCAGGTGCCACCATGCCCGACTAATTTTT A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE38233;GSE99789;GSE107867;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;esophageal squamous carcinoma cells,EC109;ASD brains,temporal_cortex;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29796672,30559470,32596459 RNA-Seq:(High) rs1272239539 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5896 RMVar_ID_5896 Human_SNP_ID_730558771 A-to-I Human chrX + 123909216 123909216 123909216 ATGCCCGACTAATTTTTTTTTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGGTA ATGCCCGACTAATTTTTTTTTATTTTTAGTAGGGACGGGGTTTCACCATGTTGGCCAGGCTGGTA A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1426701810 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5897 RMVar_ID_5897 Human_SNP_ID_730558780 A-to-I Human chrX + 123909231 123909231 123909231 TTTTTTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGGTATCAAACTCCTGACCT TTTTTTATTTTTAGTAGAGACGGGGTTTCACCGTGTTGGCCAGGCTGGTATCAAACTCCTGACCT A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line - 23474544,24183664,29129909,29796672,31158229 RNA-Seq:(High) rs1362178795 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5898 RMVar_ID_5898 Human_SNP_ID_730558790 A-to-I Human chrX + 123909251 123909251 123909251 CGGGGTTTCACCATGTTGGCCAGGCTGGTATCAAACTCCTGACCTCAAGAGATCCACTCGCCTTG CGGGGTTTCACCATGTTGGCCAGGCTGGTATCGAACTCCTGACCTCAAGAGATCCACTCGCCTTG A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1187995802 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5899 RMVar_ID_5899 Human_SNP_ID_730558793 A-to-I Human chrX + 123909265 123909264 123909266 GTTGGCCAGGCTGGTATCAAACTCCTGACCTCAAGAGATCCACTCGCCTTGCCCTCCCAAAGTGC GTTGGCCAGGCTGGTATCAAACTCCTGACCTC__GAGATCCACTCGCCTTGCCCTCCCAAAGTGC CAA C XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE100210;GSE99789;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490829,GSM3490830,GSM3490831 HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,EC109 cell line - 29129909,29796672,31158229,32596459 RNA-Seq:(High) rs1156961909 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5900 RMVar_ID_5900 Human_SNP_ID_730558797 A-to-I Human chrX + 123909274 123909274 123909274 GCTGGTATCAAACTCCTGACCTCAAGAGATCCACTCGCCTTGCCCTCCCAAAGTGCTGGGATTAC GCTGGTATCAAACTCCTGACCTCAAGAGATCCTCTCGCCTTGCCCTCCCAAAGTGCTGGGATTAC A T XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE123020:GSM3490829,GSM3490830,GSM3490831 esophageal squamous carcinoma cells,EC109 cell line - 32596459 RNA-Seq:(High) rs1454515447 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5901 RMVar_ID_5901 Human_SNP_ID_730559150 A-to-I Human chrX + 123910721 123910721 123910721 GAAACCCCGTCTCTACTAAAAAACAGAAAATTAGCCGGGCGTGGTGGCGGGCGCCTGTAGTCCCA GAAACCCCGTCTCTACTAAAAAACAGAAAATTGGCCGGGCGTGGTGGCGGGCGCCTGTAGTCCCA A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE38233;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;Bronchiolar epithelium,BERP35T4 cell line - 24183664,31158229 RNA-Seq:(High) rs1184318384 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5902 RMVar_ID_5902 Human_SNP_ID_730559180 A-to-I Human chrX + 123910800 123910800 123910800 TGAGGCAGGAGAATGGTGTGAACCCGGGAGGCAGAGCTTGCAGTGAGCCGAGATCTCGCCACTGC TGAGGCAGGAGAATGGTGTGAACCCGGGAGGCGGAGCTTGCAGTGAGCCGAGATCTCGCCACTGC A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1490234402 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5903 RMVar_ID_5903 Human_SNP_ID_730559357 A-to-I Human chrX + 123911288 123911288 123911288 TCACCTGAGGTCGGGAGGTCGAGACCAGCCTGACCAACATGGAGAAACCCCGTCTCTACTAAAAA TCACCTGAGGTCGGGAGGTCGAGACCAGCCTGGCCAACATGGAGAAACCCCGTCTCTACTAAAAA A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1308130728 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_267327,Human_miRNA_ID_1544735,Human_miRNA_ID_1597298 RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5904 RMVar_ID_5904 Human_SNP_ID_730559691 A-to-I Human chrX + 123912458 123912458 123912458 AAGTATATGATGCCAGCCTGGACAAAAGGCAAAACCCTGTCTCTACAAAAAATACAAAAATTAGC AAGTATATGATGCCAGCCTGGACAAAAGGCAAGACCCTGTCTCTACAAAAAATACAAAAATTAGC A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270221863 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9243054 Human_miRNA_ID_728549 RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5905 RMVar_ID_5905 Human_SNP_ID_730559696 A-to-I Human chrX + 123912470 123912470 123912470 CCAGCCTGGACAAAAGGCAAAACCCTGTCTCTACAAAAAATACAAAAATTAGCTGGGCATGGTGG CCAGCCTGGACAAAAGGCAAAACCCTGTCTCTGCAAAAAATACAAAAATTAGCTGGGCATGGTGG A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1333797050 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5906 RMVar_ID_5906 Human_SNP_ID_730559699 A-to-I Human chrX + 123912476 123912476 123912476 TGGACAAAAGGCAAAACCCTGTCTCTACAAAAAATACAAAAATTAGCTGGGCATGGTGGTGTGTG TGGACAAAAGGCAAAACCCTGTCTCTACAAAACATACAAAAATTAGCTGGGCATGGTGGTGTGTG A C XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs755335432 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_188084 Clinvar_Rec_39 RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5907 RMVar_ID_5907 Human_SNP_ID_730559700 A-to-I Human chrX + 123912476 123912476 123912476 TGGACAAAAGGCAAAACCCTGTCTCTACAAAAAATACAAAAATTAGCTGGGCATGGTGGTGTGTG TGGACAAAAGGCAAAACCCTGTCTCTACAAAATATACAAAAATTAGCTGGGCATGGTGGTGTGTG A T XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs755335432 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_188084 Clinvar_Rec_39 RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5908 RMVar_ID_5908 Human_SNP_ID_730559702 A-to-I Human chrX + 123912479 123912479 123912479 ACAAAAGGCAAAACCCTGTCTCTACAAAAAATACAAAAATTAGCTGGGCATGGTGGTGTGTGCCT ACAAAAGGCAAAACCCTGTCTCTACAAAAAATGCAAAAATTAGCTGGGCATGGTGGTGTGTGCCT A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs190306615 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26574684 RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5909 RMVar_ID_5909 Human_SNP_ID_730559707 A-to-I Human chrX + 123912488 123912488 123912488 AAAACCCTGTCTCTACAAAAAATACAAAAATTAGCTGGGCATGGTGGTGTGTGCCTGTAGTCCTG AAAACCCTGTCTCTACAAAAAATACAAAAATTGGCTGGGCATGGTGGTGTGTGCCTGTAGTCCTG A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs181987556 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26574684 Human_miRNA_ID_2429529,Human_miRNA_ID_2489329 RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5910 RMVar_ID_5910 Human_SNP_ID_730559718 A-to-I Human chrX + 123912524 123912524 123912524 GGGCATGGTGGTGTGTGCCTGTAGTCCTGGCTACTCCGGAGCCTGAGGTGGGAGGATCGCTTGAG GGGCATGGTGGTGTGTGCCTGTAGTCCTGGCTGCTCCGGAGCCTGAGGTGGGAGGATCGCTTGAG A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1323228713 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_727410,Human_RBP_ID_8932615,Human_RBP_ID_17580508,Human_RBP_ID_26573945 RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5911 RMVar_ID_5911 Human_SNP_ID_730559730 A-to-I Human chrX + 123912567 123912567 123912567 TGAGGTGGGAGGATCGCTTGAGTCTGGGAGGCAGAGGCTGCATTGAGCTATGATCATGGCACTGC TGAGGTGGGAGGATCGCTTGAGTCTGGGAGGCGGAGGCTGCATTGAGCTATGATCATGGCACTGC A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE38233;GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,32596459 RNA-Seq:(High) rs769405965 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7972874,Human_RBP_ID_16811689,Human_RBP_ID_17580508,Human_RBP_ID_26573945 RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5912 RMVar_ID_5912 Human_SNP_ID_730559736 A-to-I Human chrX + 123912590 123912590 123912590 CTGGGAGGCAGAGGCTGCATTGAGCTATGATCATGGCACTGCATTCCAGCCTGGGTGACAGTGCA CTGGGAGGCAGAGGCTGCATTGAGCTATGATCGTGGCACTGCATTCCAGCCTGGGTGACAGTGCA A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,31158229,31158229,31158229,32596459 RNA-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 5913 RMVar_ID_5913 Human_SNP_ID_730559789 A-to-I Human chrX + 123912728 123912728 123912728 TTTTTAATTTAAACAGTCTCACTGTGTTGCCCAGGATGGAGTGCAATGGCACAATCTTGGCTCAT TTTTTAATTTAAACAGTCTCACTGTGTTGCCCGGGATGGAGTGCAATGGCACAATCTTGGCTCAT A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1161978205 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7972875,Human_RBP_ID_17580150 Human_miRNA_ID_256137,Human_miRNA_ID_1160163,Human_miRNA_ID_2041952,Human_miRNA_ID_2275852,Human_miRNA_ID_2401746,Human_miRNA_ID_2495672,Human_miRNA_ID_2501594,Human_miRNA_ID_3020930,Human_miRNA_ID_3109622,Human_miRNA_ID_3111070 RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5914 RMVar_ID_5914 Human_SNP_ID_730559791 A-to-I Human chrX + 123912740 123912740 123912740 ACAGTCTCACTGTGTTGCCCAGGATGGAGTGCAATGGCACAATCTTGGCTCATGGCAAACTCTGC ACAGTCTCACTGTGTTGCCCAGGATGGAGTGCGATGGCACAATCTTGGCTCATGGCAAACTCTGC A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE47997;GSE38233;GSE38233;GSE38233;GSE100210;GSE107867;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;cultured B-cells;cultured B-cells;cultured B-cells;HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank;ASD brains,temporal_cortex;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,24183664,24183664,24183664,29129909,30559470,30559470,31158229,31158229,31158229,31158229,31158229 RNA-Seq:(High) rs1399488429 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17580150,Human_RBP_ID_26574686 Human_miRNA_ID_687417,Human_miRNA_ID_890021,Human_miRNA_ID_1066588,Human_miRNA_ID_1077928,Human_miRNA_ID_2275852,Human_miRNA_ID_2401746,Human_miRNA_ID_2495672,Human_miRNA_ID_2501594,Human_miRNA_ID_3109622,Human_miRNA_ID_3111070 RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5915 RMVar_ID_5915 Human_SNP_ID_730559794 A-to-I Human chrX + 123912746 123912746 123912746 TCACTGTGTTGCCCAGGATGGAGTGCAATGGCACAATCTTGGCTCATGGCAAACTCTGCCTCGCA TCACTGTGTTGCCCAGGATGGAGTGCAATGGCGCAATCTTGGCTCATGGCAAACTCTGCCTCGCA A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE107867 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;ASD brains,temporal_cortex - 23474544,24183664,29129909,30559470 RNA-Seq:(High) rs777587060 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17580150,Human_RBP_ID_26574686 Human_miRNA_ID_630620,Human_miRNA_ID_1503594 RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5916 RMVar_ID_5916 Human_SNP_ID_730559796 A-to-I Human chrX + 123912748 123912748 123912748 ACTGTGTTGCCCAGGATGGAGTGCAATGGCACAATCTTGGCTCATGGCAAACTCTGCCTCGCAAG ACTGTGTTGCCCAGGATGGAGTGCAATGGCACGATCTTGGCTCATGGCAAACTCTGCCTCGCAAG A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE47997;GSE38233;GSE38233;GSE100210;GSE100210;GSE99789;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831 K562 cells&HepG2 cells;cultured B-cells;cultured B-cells;HepG2 cell line;HepG2 cell line;esophageal squamous carcinoma cells,EC109;ASD brains,temporal_cortex;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line - 23474544,24183664,24183664,29129909,29129909,29796672,30559470,31158229,31158229,31158229,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs746759024 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17580150,Human_RBP_ID_26574686 Human_miRNA_ID_630620,Human_miRNA_ID_1503594 RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5917 RMVar_ID_5917 Human_SNP_ID_730559809 A-to-I Human chrX + 123912778 123912778 123912778 ACAATCTTGGCTCATGGCAAACTCTGCCTCGCAAGCAGCTGGGACTACAGGCATGCTCCACGGTG ACAATCTTGGCTCATGGCAAACTCTGCCTCGCCAGCAGCTGGGACTACAGGCATGCTCCACGGTG A C XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1199923618 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17580509,Human_RBP_ID_26568887 Human_miRNA_ID_583407,Human_miRNA_ID_683522 RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5918 RMVar_ID_5918 Human_SNP_ID_730559813 A-to-I Human chrX + 123912789 123912789 123912789 TCATGGCAAACTCTGCCTCGCAAGCAGCTGGGACTACAGGCATGCTCCACGGTGCCCAGTTAATT TCATGGCAAACTCTGCCTCGCAAGCAGCTGGGGCTACAGGCATGCTCCACGGTGCCCAGTTAATT A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444306240 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17580509,Human_RBP_ID_26568887 Human_miRNA_ID_277892,Human_miRNA_ID_583407 RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5919 RMVar_ID_5919 Human_SNP_ID_730559816 A-to-I Human chrX + 123912792 123912792 123912792 TGGCAAACTCTGCCTCGCAAGCAGCTGGGACTACAGGCATGCTCCACGGTGCCCAGTTAATTTTT TGGCAAACTCTGCCTCGCAAGCAGCTGGGACTGCAGGCATGCTCCACGGTGCCCAGTTAATTTTT A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE38233;GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,32596459,32596459 RNA-Seq:(High) rs748757861 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17580509 Human_miRNA_ID_277892,Human_miRNA_ID_583407,Human_miRNA_ID_605582,Human_miRNA_ID_1401067 RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5920 RMVar_ID_5920 Human_SNP_ID_730559817 A-to-I Human chrX + 123912794 123912794 123912794 GCAAACTCTGCCTCGCAAGCAGCTGGGACTACAGGCATGCTCCACGGTGCCCAGTTAATTTTTTT GCAAACTCTGCCTCGCAAGCAGCTGGGACTACGGGCATGCTCCACGGTGCCCAGTTAATTTTTTT A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350264359 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_277892,Human_miRNA_ID_605582,Human_miRNA_ID_1401067,Human_miRNA_ID_1699268 RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5921 RMVar_ID_5921 Human_SNP_ID_730559830 A-to-I Human chrX + 123912830 123912830 123912830 ATGCTCCACGGTGCCCAGTTAATTTTTTTTGTATTCTTAGTAGAGACAGGGTTTCACCATGTTGG ATGCTCCACGGTGCCCAGTTAATTTTTTTTGTGTTCTTAGTAGAGACAGGGTTTCACCATGTTGG A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,29796672,31158229,31158229,32596459 RNA-Seq:(High) rs774754642 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_186375 Human_miRNA_ID_758349,Human_miRNA_ID_1180863,Human_miRNA_ID_1635224,Human_miRNA_ID_1675719 RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5922 RMVar_ID_5922 Human_SNP_ID_730559832 A-to-I Human chrX + 123912836 123912836 123912836 CACGGTGCCCAGTTAATTTTTTTTGTATTCTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGC CACGGTGCCCAGTTAATTTTTTTTGTATTCTTCGTAGAGACAGGGTTTCACCATGTTGGCCAGGC A C XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE38233;GSE100210;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,cerebellum - 24183664,29129909,30559470 RNA-Seq:(High) rs1350924090 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5923 RMVar_ID_5923 Human_SNP_ID_730559833 A-to-I Human chrX + 123912836 123912836 123912836 CACGGTGCCCAGTTAATTTTTTTTGTATTCTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGC CACGGTGCCCAGTTAATTTTTTTTGTATTCTTGGTAGAGACAGGGTTTCACCATGTTGGCCAGGC A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE38233;GSE100210;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,cerebellum - 24183664,29129909,30559470 RNA-Seq:(High) rs1350924090 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5924 RMVar_ID_5924 Human_SNP_ID_730559835 A-to-I Human chrX + 123912839 123912839 123912839 GGTGCCCAGTTAATTTTTTTTGTATTCTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTAG GGTGCCCAGTTAATTTTTTTTGTATTCTTAGTGGAGACAGGGTTTCACCATGTTGGCCAGGCTAG A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE99789;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;ASD brains,frontal_cortex;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,29129909,29796672,30559470,31158229,31158229,31158229,32596459,32596459 RNA-Seq:(High) rs762121592 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5925 RMVar_ID_5925 Human_SNP_ID_730559839 A-to-I Human chrX + 123912845 123912845 123912845 CAGTTAATTTTTTTTGTATTCTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTAGTCTTGA CAGTTAATTTTTTTTGTATTCTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTAGTCTTGA A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,31158229,32596459,32596459 RNA-Seq:(High) rs1256618390 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5926 RMVar_ID_5926 Human_SNP_ID_730559846 A-to-I Human chrX + 123912865 123912865 123912865 CTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTAGTCTTGAATTTCTGACCTCAAGTGATT CTTAGTAGAGACAGGGTTTCACCATGTTGGCCGGGCTAGTCTTGAATTTCTGACCTCAAGTGATT A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE38233;GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,30559470,31158229 RNA-Seq:(High) rs760882653 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5927 RMVar_ID_5927 Human_SNP_ID_730559847 A-to-I Human chrX + 123912870 123912870 123912870 TAGAGACAGGGTTTCACCATGTTGGCCAGGCTAGTCTTGAATTTCTGACCTCAAGTGATTCATCT TAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAATTTCTGACCTCAAGTGATTCATCT A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE38233;GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;ASD brains,frontal_cortex;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,30559470,31158229,31158229,31158229 RNA-Seq:(High) rs766569196 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5928 RMVar_ID_5928 Human_SNP_ID_730559856 A-to-I Human chrX + 123912906 123912906 123912906 TTGAATTTCTGACCTCAAGTGATTCATCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCACG TTGAATTTCTGACCTCAAGTGATTCATCTCCCGAAGTGCTGGGATTACAGGCGTGAGCCACCACG A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-Seq:(High) rs1167646245 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18402261 RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5929 RMVar_ID_5929 Human_SNP_ID_730559857 A-to-I Human chrX + 123912907 123912907 123912907 TGAATTTCTGACCTCAAGTGATTCATCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCACGG TGAATTTCTGACCTCAAGTGATTCATCTCCCAGAGTGCTGGGATTACAGGCGTGAGCCACCACGG A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs759563910 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18402261 RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5930 RMVar_ID_5930 Human_SNP_ID_730559858 A-to-I Human chrX + 123912920 123912920 123912920 TCAAGTGATTCATCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCACGGCCGGCTAATTTTT TCAAGTGATTCATCTCCCAAAGTGCTGGGATTGCAGGCGTGAGCCACCACGGCCGGCTAATTTTT A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs764041352 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_727414,Human_RBP_ID_18144962 Human_Splice_Rec_2233687 RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5931 RMVar_ID_5931 Human_SNP_ID_730559859 A-to-I Human chrX + 123912920 123912920 123912920 TCAAGTGATTCATCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCACGGCCGGCTAATTTTT TCAAGTGATTCATCTCCCAAAGTGCTGGGATTTCAGGCGTGAGCCACCACGGCCGGCTAATTTTT A T XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs764041352 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_727414,Human_RBP_ID_18144962 Human_Splice_Rec_2233687 RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5932 RMVar_ID_5932 Human_SNP_ID_730559863 A-to-I Human chrX + 123912929 123912929 123912929 TCATCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCACGGCCGGCTAATTTTTGTATTTTTT TCATCTCCCAAAGTGCTGGGATTACAGGCGTGGGCCACCACGGCCGGCTAATTTTTGTATTTTTT A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1303280109 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_727414,Human_RBP_ID_18144962 Human_Splice_Rec_2233687 RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5933 RMVar_ID_5933 Human_SNP_ID_730559883 A-to-I Human chrX + 123912987 123912987 123912987 ATTTTTTAGTAGTGACTGGTTTCGCGGTGTTGACCAGGCTGGTCTCGAACTCCTGATCTCAGGTG ATTTTTTAGTAGTGACTGGTTTCGCGGTGTTGTCCAGGCTGGTCTCGAACTCCTGATCTCAGGTG A T XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs977953033 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2233687 RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5934 RMVar_ID_5934 Human_SNP_ID_730559885 A-to-I Human chrX + 123912990 123912990 123912990 TTTTAGTAGTGACTGGTTTCGCGGTGTTGACCAGGCTGGTCTCGAACTCCTGATCTCAGGTGATC TTTTAGTAGTGACTGGTTTCGCGGTGTTGACCCGGCTGGTCTCGAACTCCTGATCTCAGGTGATC A C XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1569480729 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2233687 RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5935 RMVar_ID_5935 Human_SNP_ID_730559893 A-to-I Human chrX + 123913002 123913002 123913002 CTGGTTTCGCGGTGTTGACCAGGCTGGTCTCGAACTCCTGATCTCAGGTGATCTGCCTGCCTCGG CTGGTTTCGCGGTGTTGACCAGGCTGGTCTCGGACTCCTGATCTCAGGTGATCTGCCTGCCTCGG A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1376566726 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2233687 RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5936 RMVar_ID_5936 Human_SNP_ID_730559895 A-to-I Human chrX + 123913015 123913015 123913015 GTTGACCAGGCTGGTCTCGAACTCCTGATCTCAGGTGATCTGCCTGCCTCGGCCTCACAAAGTGC GTTGACCAGGCTGGTCTCGAACTCCTGATCTCGGGTGATCTGCCTGCCTCGGCCTCACAAAGTGC A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE38233;GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,32596459,32596459 RNA-Seq:(High) rs989856897 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2233687 RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5937 RMVar_ID_5937 Human_SNP_ID_730559903 A-to-I Human chrX + 123913039 123913037 123913039 CTGATCTCAGGTGATCTGCCTGCCTCGGCCTCACAAAGTGCTGGGATTACAGGTGTGAACCACTG CTGATCTCAGGTGATCTGCCTGCCTCGGCCT__CAAAGTGCTGGGATTACAGGTGTGAACCACTG TCA T XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE38233;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,32596459 RNA-Seq:(High) rs759477664 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_5050994 RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5938 RMVar_ID_5938 Human_SNP_ID_730559904 A-to-I Human chrX + 123913039 123913039 123913039 CTGATCTCAGGTGATCTGCCTGCCTCGGCCTCACAAAGTGCTGGGATTACAGGTGTGAACCACTG CTGATCTCAGGTGATCTGCCTGCCTCGGCCTCGCAAAGTGCTGGGATTACAGGTGTGAACCACTG A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE38233;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,32596459 RNA-Seq:(High) rs1275608508 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5050994 RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5939 RMVar_ID_5939 Human_SNP_ID_730559910 A-to-I Human chrX + 123913055 123913055 123913055 TGCCTGCCTCGGCCTCACAAAGTGCTGGGATTACAGGTGTGAACCACTGCTCCCGGCCTTGTGTG TGCCTGCCTCGGCCTCACAAAGTGCTGGGATTGCAGGTGTGAACCACTGCTCCCGGCCTTGTGTG A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE38233;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;esophageal squamous carcinoma cells,EC109 cell line - 24183664,32596459 RNA-Seq:(High) rs1179829771 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5940 RMVar_ID_5940 Human_SNP_ID_730559956 A-to-I Human chrX + 123913198 123913198 123913198 TGTATCTTCAAAGTAGACAAATGGCGCCGGGCACGGTGGCTCACGCCTGTAATCCCAGCAGTTTC TGTATCTTCAAAGTAGACAAATGGCGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCAGTTTC A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs192084571 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_727416,Human_RBP_ID_18144964 RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5941 RMVar_ID_5941 Human_SNP_ID_730559972 A-to-I Human chrX + 123913257 123913257 123913257 AGTTTCCGAGGCTGAGGCAGGCGGCTCACCTGAGGTCAGGAGTTGGAGACCAGCCTGGCCAACAT AGTTTCCGAGGCTGAGGCAGGCGGCTCACCTGGGGTCAGGAGTTGGAGACCAGCCTGGCCAACAT A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,29796672,31158229,32596459 RNA-Seq:(High) rs772635403 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2233688 Human_miRNA_ID_469784,Human_miRNA_ID_607916,Human_miRNA_ID_2790624,Human_miRNA_ID_2820249 RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5942 RMVar_ID_5942 Human_SNP_ID_730559974 A-to-I Human chrX + 123913262 123913262 123913262 CCGAGGCTGAGGCAGGCGGCTCACCTGAGGTCAGGAGTTGGAGACCAGCCTGGCCAACATGCTGA CCGAGGCTGAGGCAGGCGGCTCACCTGAGGTCGGGAGTTGGAGACCAGCCTGGCCAACATGCTGA A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE100210;GSE99789;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,EC109;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,29796672,30559470,31158229,31158229,32596459 RNA-Seq:(High) rs773552965 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2233688 Human_miRNA_ID_469784,Human_miRNA_ID_607916,Human_miRNA_ID_2790624,Human_miRNA_ID_2820249 RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5943 RMVar_ID_5943 Human_SNP_ID_730559980 A-to-I Human chrX + 123913276 123913276 123913276 GGCGGCTCACCTGAGGTCAGGAGTTGGAGACCAGCCTGGCCAACATGCTGAAACCCTGTCTGTAC GGCGGCTCACCTGAGGTCAGGAGTTGGAGACCGGCCTGGCCAACATGCTGAAACCCTGTCTGTAC A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs185262868 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9243055 Human_Splice_Rec_2233688 Human_miRNA_ID_274399 RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5944 RMVar_ID_5944 Human_SNP_ID_730559991 A-to-I Human chrX + 123913315 123913315 123913315 CCAACATGCTGAAACCCTGTCTGTACAAAAATACAAAAATAGCTGGGCATGGTGGCGCATGCCTG CCAACATGCTGAAACCCTGTCTGTACAAAAATGCAAAAATAGCTGGGCATGGTGGCGCATGCCTG A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE47997;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 23474544,29129909,29796672,31158229,31158229 RNA-Seq:(High) rs771119064 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5051003,Human_RBP_ID_18144965,Human_RBP_ID_18402265 Human_Splice_Rec_2233688 RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5945 RMVar_ID_5945 Human_SNP_ID_730559992 A-to-I Human chrX + 123913317 123913317 123913317 AACATGCTGAAACCCTGTCTGTACAAAAATACAAAAATAGCTGGGCATGGTGGCGCATGCCTGTA AACATGCTGAAACCCTGTCTGTACAAAAATACGAAAATAGCTGGGCATGGTGGCGCATGCCTGTA A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs776739092 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18144965,Human_RBP_ID_18402265 Human_Splice_Rec_2233688 Human_miRNA_ID_188087 RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5946 RMVar_ID_5946 Human_SNP_ID_730559993 A-to-I Human chrX + 123913318 123913318 123913318 ACATGCTGAAACCCTGTCTGTACAAAAATACAAAAATAGCTGGGCATGGTGGCGCATGCCTGTAG ACATGCTGAAACCCTGTCTGTACAAAAATACAGAAATAGCTGGGCATGGTGGCGCATGCCTGTAG A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs759850948 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18144965,Human_RBP_ID_18402265 Human_Splice_Rec_2233688 Human_miRNA_ID_188087 RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5947 RMVar_ID_5947 Human_SNP_ID_730559996 A-to-I Human chrX + 123913323 123913323 123913323 CTGAAACCCTGTCTGTACAAAAATACAAAAATAGCTGGGCATGGTGGCGCATGCCTGTAGTCCCA CTGAAACCCTGTCTGTACAAAAATACAAAAATGGCTGGGCATGGTGGCGCATGCCTGTAGTCCCA A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line - 23474544,24183664,29129909,29796672,31158229,32596459 RNA-Seq:(High) rs765199563 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18144965,Human_RBP_ID_18402265 Human_Splice_Rec_2233688 RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5948 RMVar_ID_5948 Human_SNP_ID_730559999 A-to-I Human chrX + 123913331 123913331 123913331 CTGTCTGTACAAAAATACAAAAATAGCTGGGCATGGTGGCGCATGCCTGTAGTCCCAGCTACTAG CTGTCTGTACAAAAATACAAAAATAGCTGGGCGTGGTGGCGCATGCCTGTAGTCCCAGCTACTAG A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1235831543 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9243056,Human_RBP_ID_18144965 Human_Splice_Rec_2233688 RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5949 RMVar_ID_5949 Human_SNP_ID_730560006 A-to-I Human chrX + 123913349 123913349 123913349 AAAAATAGCTGGGCATGGTGGCGCATGCCTGTAGTCCCAGCTACTAGAGCGACTGAGGCAGGAGA AAAAATAGCTGGGCATGGTGGCGCATGCCTGTGGTCCCAGCTACTAGAGCGACTGAGGCAGGAGA A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1037333297 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9243056,Human_RBP_ID_24327190 Human_miRNA_ID_277871,Human_miRNA_ID_2422754 RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5950 RMVar_ID_5950 Human_SNP_ID_730560009 A-to-I Human chrX + 123913376 123913376 123913376 CCTGTAGTCCCAGCTACTAGAGCGACTGAGGCAGGAGAATTGCTTGAACCTGGGAGGCGGAGGTT CCTGTAGTCCCAGCTACTAGAGCGACTGAGGCGGGAGAATTGCTTGAACCTGGGAGGCGGAGGTT A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs752887647 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7972882,Human_RBP_ID_9243056,Human_RBP_ID_16811699,Human_RBP_ID_24327190 Human_miRNA_ID_1200754,Human_miRNA_ID_1350736,Human_miRNA_ID_2743245 RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5951 RMVar_ID_5951 Human_SNP_ID_730560012 A-to-I Human chrX + 123913390 123913390 123913390 TACTAGAGCGACTGAGGCAGGAGAATTGCTTGAACCTGGGAGGCGGAGGTTGCAGGGAGCCAAGA TACTAGAGCGACTGAGGCAGGAGAATTGCTTGGACCTGGGAGGCGGAGGTTGCAGGGAGCCAAGA A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1468978749 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16811699 Human_miRNA_ID_1465577,Human_miRNA_ID_2743245 RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5952 RMVar_ID_5952 Human_SNP_ID_730560023 A-to-I Human chrX + 123913419 123913419 123913419 TTGAACCTGGGAGGCGGAGGTTGCAGGGAGCCAAGATGGCGCCACCGCACTCCAGCCTAGGTGAT TTGAACCTGGGAGGCGGAGGTTGCAGGGAGCCGAGATGGCGCCACCGCACTCCAGCCTAGGTGAT A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE100210;GSE107867;GSE107867;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490829,GSM3490830,GSM3490831 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;ASD brains,temporal_cortex;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,EC109 cell line - 29129909,30559470,30559470,30559470,31158229,31158229,32596459 RNA-Seq:(High) rs1323545188 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5953 RMVar_ID_5953 Human_SNP_ID_730560033 A-to-I Human chrX + 123913445 123913445 123913445 GGAGCCAAGATGGCGCCACCGCACTCCAGCCTAGGTGATAGAGTGAGACTCCCTCTCAAAAACAA GGAGCCAAGATGGCGCCACCGCACTCCAGCCTGGGTGATAGAGTGAGACTCCCTCTCAAAAACAA A G XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs182574700 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 5954 RMVar_ID_5954 Human_SNP_ID_730576481 A-to-I Human chrX + 123999574 123999574 123999574 TCAAGTGATTCTCTGGCCTCAGCCACCCAAGTAGCTGGGACTACGGGTGTGTGTCCCCATGTATG TCAAGTGATTCTCTGGCCTCAGCCACCCAAGTGGCTGGGACTACGGGTGTGTGTCCCCATGTATG A G STAG2 Ensembl:ENSG00000101972 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs942632771 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_263729,RMVar_hsa_circ_117204 5955 RMVar_ID_5955 Human_SNP_ID_730576793 A-to-I Human chrX + 124001108 124001108 124001108 TATTGAAGAAGAAAAAAAATTTTTTTTTCTTTAGAGACGGAGTCTTGCTTTGTCACCCAGGCTGG TATTGAAGAAGAAAAAAAATTTTTTTTTCTTTCGAGACGGAGTCTTGCTTTGTCACCCAGGCTGG A C STAG2 Ensembl:ENSG00000101972 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1015474169 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_263729,RMVar_hsa_circ_117204 5956 RMVar_ID_5956 Human_SNP_ID_730587546 A-to-I Human chrX + 124058261 124058261 124058261 CTCACTGCAGCCTCTGCCTCCCAGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCCGAGTAGCTGGG CTCACTGCAGCCTCTGCCTCCCAGGTTCAAGCGGTTCTCCTGCCTCAGCCTCCCGAGTAGCTGGG A G STAG2 Ensembl:ENSG00000101972 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1299179814 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6628,RMVar_hsa_circ_263729,RMVar_hsa_circ_117204,RMVar_hsa_circ_14925,RMVar_hsa_circ_53320,RMVar_hsa_circ_263737,RMVar_hsa_circ_279257,RMVar_hsa_circ_266253,RMVar_hsa_circ_73424,RMVar_hsa_circ_74906,RMVar_hsa_circ_79702,RMVar_hsa_circ_263739,RMVar_hsa_circ_320824,RMVar_hsa_circ_263740,RMVar_hsa_circ_21281 5957 RMVar_ID_5957 Human_SNP_ID_730886812 A-to-I Human chrX - 125785425 125785425 125785425 ATGCAGAAAATTAGCCGGGCGTGGTGGCGGGCACCTGTGGTCCCAGCTACTCGGGAGGCTGAGGC ATGCAGAAAATTAGCCGGGCGTGGTGGCGGGCGCCTGTGGTCCCAGCTACTCGGGAGGCTGAGGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs922090162 Functional Loss SNV dbSNP153 33..33 33 - - - 5958 RMVar_ID_5958 Human_SNP_ID_731013925 A-to-I Human chrX + 126472003 126472003 126472003 CCTCCGCTACCATAATCATCGCTATTCCCACCAGCGTCAAAGTATTTAGCTGACTCGCTACACTC CCTCCGCTACCATAATCATCGCTATTCCCACCGGCGTCAAAGTATTTAGCTGACTCGCTACACTC A G MTCO1P53 Ensembl:ENSG00000230916 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs995769787 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1827218 5959 RMVar_ID_5959 Human_SNP_ID_731649601 A-to-I Human chrX - 129852044 129852044 129852044 CCCTTCTTGCCTTTCTGCTCCTGCCTATATGCATCCAGAGCTTCTTTTTTTTTTCTTTTTTTCTT CCCTTCTTGCCTTTCTGCTCCTGCCTATATGCTTCCAGAGCTTCTTTTTTTTTTCTTTTTTTCTT T A - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1176152400 Functional Loss SNV dbSNP153 33..33 33 - - - 5960 RMVar_ID_5960 Human_SNP_ID_731678367 A-to-I Human chrX + 130011269 130011269 130011269 TTGTTGTTGTTGTTGTTTTGAGACAGGGTCTCACTCTGTCGCCCAGGTTGAAGTGCAGTGGTGGG TTGTTGTTGTTGTTGTTTTGAGACAGGGTCTCTCTCTGTCGCCCAGGTTGAAGTGCAGTGGTGGG A T BCORL1 Ensembl:ENSG00000085185 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1470557224 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19552,RMVar_hsa_circ_55194,RMVar_hsa_circ_59862,RMVar_hsa_circ_41662 5961 RMVar_ID_5961 Human_SNP_ID_731714497 A-to-I Human chrX - 130207565 130207565 130207565 CTGAGGTCAGGAGTTTAAGACCAACCTGGCCAACATGGCAAAACCCCATCTCTACTAAAAATGCA CTGAGGTCAGGAGTTTAAGACCAACCTGGCCAGCATGGCAAAACCCCATCTCTACTAAAAATGCA T C ZNF280C Ensembl:ENSG00000056277 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1413483258 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_65019,RMVar_hsa_circ_70388,RMVar_hsa_circ_264839 5962 RMVar_ID_5962 Human_SNP_ID_731741106 A-to-I Human chrX + 130363924 130363924 130363924 CCTGGCTAATTTAAAAAATTTTTTTAAGAGATAGAGTCTTACTGTATTGCCCAGGTTTGTCTAGA CCTGGCTAATTTAAAAAATTTTTTTAAGAGATGGAGTCTTACTGTATTGCCCAGGTTTGTCTAGA A G SLC25A14 Ensembl:ENSG00000102078 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1428979869 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16958501 RMVar_hsa_circ_94128,RMVar_hsa_circ_263875 5963 RMVar_ID_5963 Human_SNP_ID_731741110 A-to-I Human chrX + 130363954 130363954 130363954 ATAGAGTCTTACTGTATTGCCCAGGTTTGTCTAGAACTCCTCCTCAAGTGATCCTCCTGCCTCAC ATAGAGTCTTACTGTATTGCCCAGGTTTGTCTGGAACTCCTCCTCAAGTGATCCTCCTGCCTCAC A G SLC25A14 Ensembl:ENSG00000102078 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027492374 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16818292 RMVar_hsa_circ_94128,RMVar_hsa_circ_263875 5964 RMVar_ID_5964 Human_SNP_ID_731763604 A-to-I Human chrX + 130496267 130496264 130496268 GTGTGACAGAACGTATCACTGATGACTGATAGAAAGCCCTCTTTCACTCTGATTACCCACTCACT GTGTGACAGAACGTATCACTGATGACTGAT____AGCCCTCTTTCACTCTGATTACCCACTCACT TAGAA T DENND10P1 Ensembl:ENSG00000221930 Pseudogene exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs778254003 Functional Loss DEL dbSNP153 31..34 33 - - - RMVar_hsa_circ_268525 5965 RMVar_ID_5965 Human_SNP_ID_731974289 A-to-I Human chrX - 131704908 131704908 131704908 GGAGTCCTTGCTTAGTCTCGTTTGAGGCTTTAAAAGAGACCTGGACATTGGCGGTACCTTGGTAT GGAGTCCTTGCTTAGTCTCGTTTGAGGCTTTAGAAGAGACCTGGACATTGGCGGTACCTTGGTAT T C FIRRE Ensembl:ENSG00000213468 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041155136 Functional Loss SNV dbSNP153 33..33 33 - - - 5966 RMVar_ID_5966 Human_SNP_ID_731979929 A-to-I Human chrX - 131734617 131734617 131734617 AAAAGAGACCTGGACATTGGCAATATCTTGCTATAGAACCTGGAGTGTGAAGCTTCTAATAACAA AAAAGAGACCTGGACATTGGCAATATCTTGCTGTAGAACCTGGAGTGTGAAGCTTCTAATAACAA T C FIRRE Ensembl:ENSG00000213468 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913820361 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5640050 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 5967 RMVar_ID_5967 Human_SNP_ID_731980842 A-to-I Human chrX - 131739506 131739494 131739506 ACTTGTTTTAACAGCTATAGTACATGGTGGCCAGTCAAGGTGCCTCGTGCCTGTAATCCTAGCAC ACTTGTTTTAACAGCTATAGTACATGGTGGCC____________TCGTGCCTGTAATCCTAGCAC AGGCACCTTGACT A FIRRE Ensembl:ENSG00000213468 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1452505113 Functional Loss DEL dbSNP153 33..44 33 - - - Human_RBP_ID_3931684 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 5968 RMVar_ID_5968 Human_SNP_ID_731981243 A-to-I Human chrX - 131741713 131741713 131741713 AAAGGACACCAGGACTTTGGCGGTGTCTTGGTATAGAACCTGGAGTGTGAAGGTTCTAATACCAA AAAGGACACCAGGACTTTGGCGGTGTCTTGGTGTAGAACCTGGAGTGTGAAGGTTCTAATACCAA T C FIRRE Ensembl:ENSG00000213468 lincRNA intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs939025250 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 5969 RMVar_ID_5969 Human_SNP_ID_731981731 A-to-I Human chrX - 131743913 131743913 131743913 TACTTGGGAGGCTGAGGCAGGAGAATGGCGTGAACTCGGGAGGTAGAGCTTGCAGTAAGCCAAGA TACTTGGGAGGCTGAGGCAGGAGAATGGCGTGCACTCGGGAGGTAGAGCTTGCAGTAAGCCAAGA T G FIRRE Ensembl:ENSG00000213468 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1292318446 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,RMVar_hsa_circ_315484 5970 RMVar_ID_5970 Human_SNP_ID_731981740 A-to-I Human chrX - 131743954 131743954 131743954 AAAATTAGCGGGGCGTGTTGGCAGGCGCCTGTAGTCCCAGGTACTTGGGAGGCTGAGGCAGGAGA AAAATTAGCGGGGCGTGTTGGCAGGCGCCTGTTGTCCCAGGTACTTGGGAGGCTGAGGCAGGAGA T A FIRRE Ensembl:ENSG00000213468 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1569458660 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,RMVar_hsa_circ_315484 5971 RMVar_ID_5971 Human_SNP_ID_731981988 A-to-I Human chrX - 131745521 131745521 131745521 GTATTTTTAGTAGAGACGGGTTTCACCATTTTAGCCAGGATGGTCTCAATCTCCTTACCTTGTGA GTATTTTTAGTAGAGACGGGTTTCACCATTTTGGCCAGGATGGTCTCAATCTCCTTACCTTGTGA T C FIRRE Ensembl:ENSG00000213468 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1304535084 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,RMVar_hsa_circ_315484 5972 RMVar_ID_5972 Human_SNP_ID_731982042 A-to-I Human chrX - 131745814 131745814 131745814 TACTGGGTGGCCGGGCATGACACCTCATGCCTATAATCCTAGCACTTTGGGAGTCTGAGATAGGA TACTGGGTGGCCGGGCATGACACCTCATGCCTGTAATCCTAGCACTTTGGGAGTCTGAGATAGGA T C FIRRE Ensembl:ENSG00000213468 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334794315 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,RMVar_hsa_circ_315484 5973 RMVar_ID_5973 Human_SNP_ID_731982379 A-to-I Human chrX - 131747888 131747888 131747888 CTCCTACCTGAGACTCTTGAGTAGCTGAGATTACAGACGCCCGCCACCACCCCCAGCTAATTTTT CTCCTACCTGAGACTCTTGAGTAGCTGAGATTGCAGACGCCCGCCACCACCCCCAGCTAATTTTT T C FIRRE Ensembl:ENSG00000213468 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1308236288 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16819257 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,RMVar_hsa_circ_315484 5974 RMVar_ID_5974 Human_SNP_ID_731991296 A-to-I Human chrX - 131794418 131794418 131794418 ATGTTCTTCAAGCTGCTCTGCTCCTGGGCCCAAGCTATTCTCCTGCCTCAGCCTTCCAAGAAGCT ATGTTCTTCAAGCTGCTCTGCTCCTGGGCCCAGGCTATTCTCCTGCCTCAGCCTTCCAAGAAGCT T C FIRRE Ensembl:ENSG00000213468 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1401424277 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1064195,Human_RBP_ID_2070409,Human_RBP_ID_3931693,Human_RBP_ID_5052320,Human_RBP_ID_18915431,Human_RBP_ID_26301171 Human_Splice_Rec_2236208,Human_Splice_Rec_2236209,Human_Splice_Rec_2236247,Human_Splice_Rec_2236267,Human_Splice_Rec_2236289,Human_Splice_Rec_2236313,Human_Splice_Rec_2236330,Human_Splice_Rec_2236391,Human_Splice_Rec_2236392,Human_Splice_Rec_2236418,Human_Splice_Rec_2236424 RMVar_hsa_circ_311647,RMVar_hsa_circ_263890,RMVar_hsa_circ_299007,RMVar_hsa_circ_263891,RMVar_hsa_circ_314230,RMVar_hsa_circ_91211,RMVar_hsa_circ_263892,RMVar_hsa_circ_263893,RMVar_hsa_circ_321134,RMVar_hsa_circ_266281,RMVar_hsa_circ_124553,RMVar_hsa_circ_263906,RMVar_hsa_circ_267739,RMVar_hsa_circ_263903,RMVar_hsa_circ_325060,RMVar_hsa_circ_263905,RMVar_hsa_circ_268805,RMVar_hsa_circ_372124,RMVar_hsa_circ_324976,RMVar_hsa_circ_127990,RMVar_hsa_circ_263908,RMVar_hsa_circ_263907,RMVar_hsa_circ_87070,RMVar_hsa_circ_118974,RMVar_hsa_circ_263912,RMVar_hsa_circ_116178,RMVar_hsa_circ_96057,RMVar_hsa_circ_263914,RMVar_hsa_circ_263915,RMVar_hsa_circ_112193,RMVar_hsa_circ_124030,RMVar_hsa_circ_263916,RMVar_hsa_circ_263917,RMVar_hsa_circ_263919,RMVar_hsa_circ_114646,RMVar_hsa_circ_263918 5975 RMVar_ID_5975 Human_SNP_ID_732064575 A-to-I Human chrX - 132210457 132210457 132210457 ATTTTACATGGCAGCAGAATGCCTGGGATGCTAACAAAGGCTACTGAAAGACTAAACTCTATTTG ATTTTACATGGCAGCAGAATGCCTGGGATGCTGACAAAGGCTACTGAAAGACTAAACTCTATTTG T C RAP2C Ensembl:ENSG00000123728 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs967726278 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17580172,Human_RBP_ID_23317411 RMVar_hsa_circ_87393,RMVar_hsa_circ_263922 5976 RMVar_ID_5976 Human_SNP_ID_732071993 A-to-I Human chrX + 132254308 132254308 132254308 TTATTTTACTTTTAGAAACAGAGTCTCACTCTATCACTCAGGCTGGAGTGTAGTGGTGCGATTAT TTATTTTACTTTTAGAAACAGAGTCTCACTCTGTCACTCAGGCTGGAGTGTAGTGGTGCGATTAT A G RAP2C-AS1 Ensembl:ENSG00000232160 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs895520194 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_263925 5977 RMVar_ID_5977 Human_SNP_ID_732100457 A-to-I Human chrX + 132430282 132430282 132430282 AAAATCGCAAAAATAATACCTGGAGTCCCTGTATACCCTTCACCCAGATTCCCCTACTGTTAAAT AAAATCGCAAAAATAATACCTGGAGTCCCTGTGTACCCTTCACCCAGATTCCCCTACTGTTAAAT A G RAP2C-AS1 Ensembl:ENSG00000232160 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1344199867 Functional Loss SNV dbSNP153 33..33 33 - - - 5978 RMVar_ID_5978 Human_SNP_ID_732430228 A-to-I Human chrX + 134418901 134418901 134418901 ATCTGACTCTGTTGTCCAGGCTGGAGTGCAGTAGTGTGATCATGACTCACTGCAGCCTTGACCTT ATCTGACTCTGTTGTCCAGGCTGGAGTGCAGTGGTGTGATCATGACTCACTGCAGCCTTGACCTT A G PHF6 Ensembl:ENSG00000156531 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1268594688 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7734,RMVar_hsa_circ_122191,RMVar_hsa_circ_263941,RMVar_hsa_circ_109681,RMVar_hsa_circ_8894,RMVar_hsa_circ_2946,RMVar_hsa_circ_263943,RMVar_hsa_circ_27339,RMVar_hsa_circ_302226 5979 RMVar_ID_5979 Human_SNP_ID_732489090 A-to-I Human chrX - 134777431 134777428 134777432 ACCTCTGCTTCCCGGGCTCAAGCCATCCACCCACCTCGGCCTCCCGAATAGCTGGGACTACAGGT ACCTCTGCTTCCCGGGCTCAAGCCATCCACC____TCGGCCTCCCGAATAGCTGGGACTACAGGT AGGTG A FAM122B Ensembl:ENSG00000156504 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1489090620 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_16827628 5980 RMVar_ID_5980 Human_SNP_ID_732489477 A-to-I Human chrX - 134779172 134779172 134779172 CACCTACCTTGGCCTCCCAAAGTGTTGGGATTATAGGCATGAGCCACTGCGCCTGGCCAACTTTT CACCTACCTTGGCCTCCCAAAGTGTTGGGATTGTAGGCATGAGCCACTGCGCCTGGCCAACTTTT T C FAM122B Ensembl:ENSG00000156504 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1343571099 Functional Loss SNV dbSNP153 33..33 33 - - - 5981 RMVar_ID_5981 Human_SNP_ID_732498985 A-to-I Human chrX + 134835787 134835787 134835787 GTGATCCTCTTGCCTCAGCCTCCCAACTAGCTAGGACTACAGGTGCACACCACTATGCCTGGATA GTGATCCTCTTGCCTCAGCCTCCCAACTAGCTCGGACTACAGGTGCACACCACTATGCCTGGATA A C FAM122C Ensembl:ENSG00000156500 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs774488388 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2237364,Human_Splice_Rec_2237428,Human_Splice_Rec_2237471 5982 RMVar_ID_5982 Human_SNP_ID_732499041 A-to-I Human chrX + 134836057 134836057 134836057 ACGGGGTTTCACCATATTGGTCCGACTGGTCTAGAACTCCTGACCTCAGGTGATCCACCCGCCTC ACGGGGTTTCACCATATTGGTCCGACTGGTCTGGAACTCCTGACCTCAGGTGATCCACCCGCCTC A G FAM122C Ensembl:ENSG00000156500 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1169668300 Functional Loss SNV dbSNP153 33..33 33 - - - 5983 RMVar_ID_5983 Human_SNP_ID_732500067 A-to-I Human chrX + 134840975 134840975 134840975 GGTCAAATATTTATTTATGTATTTATTTATTTATTGAGACAGGGTCTCATATTGTTGCCAGGCTG GGTCAAATATTTATTTATGTATTTATTTATTTTTTGAGACAGGGTCTCATATTGTTGCCAGGCTG A T FAM122C Ensembl:ENSG00000156500 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs975615008 Functional Loss SNV dbSNP153 33..33 33 - - - 5984 RMVar_ID_5984 Human_SNP_ID_732500068 A-to-I Human chrX + 134840983 134840983 134840983 ATTTATTTATGTATTTATTTATTTATTGAGACAGGGTCTCATATTGTTGCCAGGCTGGAGTGCAG ATTTATTTATGTATTTATTTATTTATTGAGACGGGGTCTCATATTGTTGCCAGGCTGGAGTGCAG A G FAM122C Ensembl:ENSG00000156500 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1211030962 Functional Loss SNV dbSNP153 33..33 33 - - - 5985 RMVar_ID_5985 Human_SNP_ID_732500070 A-to-I Human chrX + 134840991 134840990 134840992 ATGTATTTATTTATTTATTGAGACAGGGTCTCATATTGTTGCCAGGCTGGAGTGCAGTGGCACAA ATGTATTTATTTATTTATTGAGACAGGGTCTC__ATTGTTGCCAGGCTGGAGTGCAGTGGCACAA CAT C FAM122C Ensembl:ENSG00000156500 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs944629422 Functional Loss DEL dbSNP153 33..34 33 - - - 5986 RMVar_ID_5986 Human_SNP_ID_732500095 A-to-I Human chrX + 134841178 134841178 134841178 GTAGAGATGAGGTCTTGTTGTTACCCAGGCTGATCTCGAACTCGTGAGCTCAAGGATTCCTCCTG GTAGAGATGAGGTCTTGTTGTTACCCAGGCTGCTCTCGAACTCGTGAGCTCAAGGATTCCTCCTG A C FAM122C Ensembl:ENSG00000156500 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs994768270 Functional Loss SNV dbSNP153 33..33 33 - - - 5987 RMVar_ID_5987 Human_SNP_ID_732500289 A-to-I Human chrX + 134842347 134842347 134842347 TTTTTTTAATTTCTCTGGGCGCGGTGGCTCACACCTGTAATCCTAGCACTTTGGGAGGCCGAGGT TTTTTTTAATTTCTCTGGGCGCGGTGGCTCACGCCTGTAATCCTAGCACTTTGGGAGGCCGAGGT A G FAM122C Ensembl:ENSG00000156500 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs891266694 Functional Loss SNV dbSNP153 33..33 33 - - - 5988 RMVar_ID_5988 Human_SNP_ID_732500319 A-to-I Human chrX + 134842487 134842487 134842487 AAAATTAGCTGGGCGTGGTGGTGGGCACCTGTAGTCCCAGCTACTCAGGAGGCTGAATCGGGAGA AAAATTAGCTGGGCGTGGTGGTGGGCACCTGTGGTCCCAGCTACTCAGGAGGCTGAATCGGGAGA A G FAM122C Ensembl:ENSG00000156500 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1300518276 Functional Loss SNV dbSNP153 33..33 33 - - - 5989 RMVar_ID_5989 Human_SNP_ID_732500365 A-to-I Human chrX + 134842711 134842710 134842711 CCTGAGGTCAGGAGTTTGAAACCAGCCTGGCCAACACGGTGAAACCCCATCTCTGCTAAACATAC CCTGAGGTCAGGAGTTTGAAACCAGCCTGGCC_ACACGGTGAAACCCCATCTCTGCTAAACATAC CA C FAM122C Ensembl:ENSG00000156500 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1347595830 Functional Loss DEL dbSNP153 33..33 33 - - - 5990 RMVar_ID_5990 Human_SNP_ID_732500448 A-to-I Human chrX + 134843084 134843084 134843084 TAGCCGGGCCTGGTGGCATGCGCCTGTAATCCAAGCTACTCAGGAGGCTGAGACAGGAGAATCGC TAGCCGGGCCTGGTGGCATGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAGACAGGAGAATCGC A C FAM122C Ensembl:ENSG00000156500 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1409358017 Functional Loss SNV dbSNP153 33..33 33 - - - 5991 RMVar_ID_5991 Human_SNP_ID_732500451 A-to-I Human chrX + 134843089 134843089 134843089 GGGCCTGGTGGCATGCGCCTGTAATCCAAGCTACTCAGGAGGCTGAGACAGGAGAATCGCTTGAA GGGCCTGGTGGCATGCGCCTGTAATCCAAGCTGCTCAGGAGGCTGAGACAGGAGAATCGCTTGAA A G FAM122C Ensembl:ENSG00000156500 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1445054652 Functional Loss SNV dbSNP153 33..33 33 - - - 5992 RMVar_ID_5992 Human_SNP_ID_732500685 A-to-I Human chrX + 134843978 134843978 134843978 AGAGTGTTGCTCTCTGTCATTCAGGCTGGAGTACAGTAGTGCAATTTCAGCTCACTGCAACCTTT AGAGTGTTGCTCTCTGTCATTCAGGCTGGAGTGCAGTAGTGCAATTTCAGCTCACTGCAACCTTT A G FAM122C Ensembl:ENSG00000156500 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1171459994 Functional Loss SNV dbSNP153 33..33 33 - - - 5993 RMVar_ID_5993 Human_SNP_ID_732500687 A-to-I Human chrX + 134843983 134843983 134843983 GTTGCTCTCTGTCATTCAGGCTGGAGTACAGTAGTGCAATTTCAGCTCACTGCAACCTTTGCCTC GTTGCTCTCTGTCATTCAGGCTGGAGTACAGTGGTGCAATTTCAGCTCACTGCAACCTTTGCCTC A G FAM122C Ensembl:ENSG00000156500 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277494231 Functional Loss SNV dbSNP153 33..33 33 - - - 5994 RMVar_ID_5994 Human_SNP_ID_732503256 A-to-I Human chrX + 134860227 134860227 134860227 GATTCTTGTGCTTCAGTCTTCTGAGTGGGACTACAGACGCATGCCACCATGCTCATTTATTCTTT GATTCTTGTGCTTCAGTCTTCTGAGTGGGACTCCAGACGCATGCCACCATGCTCATTTATTCTTT A C lnc-FAM122C-1,RF00017-4520 RNACentral:URS00008BE00C,RNACentral:URS000099C2D3 lincRNA,SRP RNA exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1245761086 Functional Loss SNV dbSNP153 33..33 33 - - - 5995 RMVar_ID_5995 Human_SNP_ID_732512014 A-to-I Human chrX - 134913195 134913195 134913195 ACTTTTTGTATGTTTAGTGGAGACAGGGTTTCACCATGTCTACCAGGCTGGTCTCGAACTCCTGA ACTTTTTGTATGTTTAGTGGAGACAGGGTTTCCCCATGTCTACCAGGCTGGTCTCGAACTCCTGA T G MOSPD1 Ensembl:ENSG00000101928 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459999965 Functional Loss SNV dbSNP153 33..33 33 - - - 5996 RMVar_ID_5996 Human_SNP_ID_463239380 A-to-I Human chr11 - 40243813 40243813 40243813 GTGGTGGCAGGAGCCTATAATCCCAGCTACTCAAGAGCTGAGGCAGGAGAATCACTTGAAGCTGA GTGGTGGCAGGAGCCTATAATCCCAGCTACTCGAGAGCTGAGGCAGGAGAATCACTTGAAGCTGA T C LRRC4C Ensembl:ENSG00000148948 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1425606298 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7529,RMVar_hsa_circ_39906,RMVar_hsa_circ_42641 5997 RMVar_ID_5997 Human_SNP_ID_463249482 A-to-I Human chr11 - 40284993 40284993 40284993 AGTGCCTCTTGTTGGTGGAGGAGATACATTCCATGATCCCCAGTGGATGCCCGAAACCACTGATA AGTGCCTCTTGTTGGTGGAGGAGATACATTCCTTGATCCCCAGTGGATGCCCGAAACCACTGATA T A LRRC4C Ensembl:ENSG00000148948 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs943722977 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7529,RMVar_hsa_circ_39906,RMVar_hsa_circ_42641 5998 RMVar_ID_5998 Human_SNP_ID_463249506 A-to-I Human chr11 - 40285102 40285102 40285102 CTAAGTGAGGATTAAGGAAAAAAATACATGTTATATTTTCAGTACAGTGCCTGGTGCATATCAAA CTAAGTGAGGATTAAGGAAAAAAATACATGTTGTATTTTCAGTACAGTGCCTGGTGCATATCAAA T C LRRC4C Ensembl:ENSG00000148948 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1012779165 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7529,RMVar_hsa_circ_39906,RMVar_hsa_circ_42641 5999 RMVar_ID_5999 Human_SNP_ID_464053121 A-to-I Human chr11 + 43320562 43320562 43320562 GCCCAGTAGTTCGAGAACAGCCTGGGCAACATAGGGAAATCCGCCTTTAAAATTAGCCAGGCGTG GCCCAGTAGTTCGAGAACAGCCTGGGCAACATGGGGAAATCCGCCTTTAAAATTAGCCAGGCGTG A G API5 Ensembl:ENSG00000166181 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs773106655 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36087,RMVar_hsa_circ_321989,RMVar_hsa_circ_322721,RMVar_hsa_circ_149209 6000 RMVar_ID_6000 Human_SNP_ID_464064447 A-to-I Human chr11 + 43365200 43365200 43365200 ATAGCTCACCGTGACCTTGAACTCCTAGGCTCAAGTGATCTTCCCACCACAACCTCCCTAGTACC ATAGCTCACCGTGACCTTGAACTCCTAGGCTCGAGTGATCTTCCCACCACAACCTCCCTAGTACC A G TTC17 Ensembl:ENSG00000052841 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1487886008 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11618485 6001 RMVar_ID_6001 Human_SNP_ID_464064771 A-to-I Human chr11 + 43366455 43366455 43366455 TTGAGCCCGGGAGGTGGAGGTTGTAGTGACCCAAGATAGTGCCACTGTACTCCAGCTTGCGTGAC TTGAGCCCGGGAGGTGGAGGTTGTAGTGACCCTAGATAGTGCCACTGTACTCCAGCTTGCGTGAC A T TTC17 Ensembl:ENSG00000052841 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1047814854 Functional Loss SNV dbSNP153 33..33 33 - - - 6002 RMVar_ID_6002 Human_SNP_ID_464079471 A-to-I Human chr11 + 43424141 43424141 43424141 GCGGAGTCTCGCTCGCTCTTGTCGCCCAGGCTAGAGTGCAGTGGCTCTGTCTCGGCTCACTGCCA GCGGAGTCTCGCTCGCTCTTGTCGCCCAGGCTGGAGTGCAGTGGCTCTGTCTCGGCTCACTGCCA A G TTC17 Ensembl:ENSG00000052841 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1302690325 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1047,RMVar_hsa_circ_19185,RMVar_hsa_circ_42649,RMVar_hsa_circ_149224,RMVar_hsa_circ_318619,RMVar_hsa_circ_60755,RMVar_hsa_circ_337228,RMVar_hsa_circ_309070,RMVar_hsa_circ_149228,RMVar_hsa_circ_149227,RMVar_hsa_circ_29733,RMVar_hsa_circ_320268,RMVar_hsa_circ_326683,RMVar_hsa_circ_103891,RMVar_hsa_circ_17953,RMVar_hsa_circ_149234,RMVar_hsa_circ_149235,RMVar_hsa_circ_149236,RMVar_hsa_circ_149233,RMVar_hsa_circ_109597,RMVar_hsa_circ_57808,RMVar_hsa_circ_149237,RMVar_hsa_circ_358125,RMVar_hsa_circ_56342,RMVar_hsa_circ_35073,RMVar_hsa_circ_49353,RMVar_hsa_circ_92549,RMVar_hsa_circ_40523,RMVar_hsa_circ_149240 6003 RMVar_ID_6003 Human_SNP_ID_464082417 A-to-I Human chr11 + 43436272 43436272 43436272 TGCTGAAGAAGAGCCCTCTGAGAGAGGAACAGAGGAGGACCCTGTATTCTCTGTTGAGAATTCAG TGCTGAAGAAGAGCCCTCTGAGAGAGGAACAGGGGAGGACCCTGTATTCTCTGTTGAGAATTCAG A G TTC17 Ensembl:ENSG00000052841 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs17853132 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3940312,Human_RBP_ID_18973449,Human_RBP_ID_27803354 Human_Splice_Rec_1230125,Human_Splice_Rec_1230165,Human_Splice_Rec_1230179 RMVar_hsa_circ_1047,RMVar_hsa_circ_19185,RMVar_hsa_circ_42649,RMVar_hsa_circ_149224,RMVar_hsa_circ_318619,RMVar_hsa_circ_60755,RMVar_hsa_circ_337228,RMVar_hsa_circ_309070,RMVar_hsa_circ_149228,RMVar_hsa_circ_149227,RMVar_hsa_circ_29733,RMVar_hsa_circ_320268,RMVar_hsa_circ_326683,RMVar_hsa_circ_103891,RMVar_hsa_circ_17953,RMVar_hsa_circ_149234,RMVar_hsa_circ_149235,RMVar_hsa_circ_149236,RMVar_hsa_circ_149233,RMVar_hsa_circ_109597,RMVar_hsa_circ_57808,RMVar_hsa_circ_149237,RMVar_hsa_circ_358125,RMVar_hsa_circ_56342,RMVar_hsa_circ_35073,RMVar_hsa_circ_49353,RMVar_hsa_circ_92549,RMVar_hsa_circ_40523,RMVar_hsa_circ_116051,RMVar_hsa_circ_149240,RMVar_hsa_circ_149241 6004 RMVar_ID_6004 Human_SNP_ID_464091634 A-to-I Human chr11 + 43475410 43475410 43475410 CTAAAGGTGCAGTGGCGTGATCACCACTCACTACAGCCTCAACCTCCCAGGTTAAAGCAATCCTT CTAAAGGTGCAGTGGCGTGATCACCACTCACTGCAGCCTCAACCTCCCAGGTTAAAGCAATCCTT A G TTC17 Ensembl:ENSG00000052841 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1194842278 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92549,RMVar_hsa_circ_149240 6005 RMVar_ID_6005 Human_SNP_ID_464091652 A-to-I Human chr11 + 43475524 43475524 43475524 CCAGCTAATTTTTAAATTTTTTAAATAGAGACAAGGTCTTCCCTGTGTTGCCCAGGTTCCTGGAC CCAGCTAATTTTTAAATTTTTTAAATAGAGACGAGGTCTTCCCTGTGTTGCCCAGGTTCCTGGAC A G TTC17 Ensembl:ENSG00000052841 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1214496899 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17559899 RMVar_hsa_circ_92549,RMVar_hsa_circ_149240 6006 RMVar_ID_6006 Human_SNP_ID_464141300 A-to-I Human chr11 + 43682871 43682871 43682871 AGTGGTGTGGTGGTGTGATCATAGCCAACTGCAGCCTCGAACTCTTGGGTTCAAGTGATCCTCCC AGTGGTGTGGTGGTGTGATCATAGCCAACTGCGGCCTCGAACTCTTGGGTTCAAGTGATCCTCCC A G AC068205.2,HSD17B12 Ensembl:ENSG00000283341,Ensembl:ENSG00000149084 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1259880453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17559901 RMVar_hsa_circ_991 6007 RMVar_ID_6007 Human_SNP_ID_464146519 A-to-I Human chr11 + 43705952 43705952 43705952 TCCCGGTTAATTTTTGTATTTTTTGTAGAGACAGGGTTTCACTATATTGCCTAGGCTGGTAGATT TCCCGGTTAATTTTTGTATTTTTTGTAGAGACGGGGTTTCACTATATTGCCTAGGCTGGTAGATT A G AC068205.2,HSD17B12 Ensembl:ENSG00000283341,Ensembl:ENSG00000149084 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903813038 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_991 6008 RMVar_ID_6008 Human_SNP_ID_464153170 A-to-I Human chr11 + 43735728 43735728 43735728 GTTGTTGTATTAGTATGTTTTCACACTGCTGTAAAGAACTACCTGAGACTCTGTCATTTATAAAG GTTGTTGTATTAGTATGTTTTCACACTGCTGTGAAGAACTACCTGAGACTCTGTCATTTATAAAG A G AC068205.2,HSD17B12 Ensembl:ENSG00000283341,Ensembl:ENSG00000149084 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1183125750 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1079776,Human_RBP_ID_11767506,Human_RBP_ID_23505248 RMVar_hsa_circ_991 6009 RMVar_ID_6009 Human_SNP_ID_464179544 A-to-I Human chr11 + 43856847 43856847 43856847 TCCCAGTTAGAAAATAGTTGTAGGCTAAGCACAGTGGCTTACACCTGTAAACTCAATGCTTTGGG TCCCAGTTAGAAAATAGTTGTAGGCTAAGCACGGTGGCTTACACCTGTAAACTCAATGCTTTGGG A G - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs913148044 Functional Loss SNV dbSNP153 33..33 33 - - - 6010 RMVar_ID_6010 Human_SNP_ID_464179547 A-to-I Human chr11 + 43856863 43856863 43856863 GTTGTAGGCTAAGCACAGTGGCTTACACCTGTAAACTCAATGCTTTGGGAGGCTGAGACAGGAGG GTTGTAGGCTAAGCACAGTGGCTTACACCTGTCAACTCAATGCTTTGGGAGGCTGAGACAGGAGG A C - - Other Unknown GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1274833194 Functional Loss SNV dbSNP153 33..33 33 - - - 6011 RMVar_ID_6011 Human_SNP_ID_464179580 A-to-I Human chr11 + 43856980 43856980 43856980 GTCTCTACAAAAAAATTAAAAAATAAAAAATTAGCCAGGTGTGGTGGCACGCACCTGTAGTCCCA GTCTCTACAAAAAAATTAAAAAATAAAAAATTGGCCAGGTGTGGTGGCACGCACCTGTAGTCCCA A G - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs55885036 Functional Loss SNV dbSNP153 33..33 33 - - - 6012 RMVar_ID_6012 Human_SNP_ID_464179591 A-to-I Human chr11 + 43857000 43857000 43857000 AAATAAAAAATTAGCCAGGTGTGGTGGCACGCACCTGTAGTCCCAGCTACTTGGAAGGCTGAGGC AAATAAAAAATTAGCCAGGTGTGGTGGCACGCCCCTGTAGTCCCAGCTACTTGGAAGGCTGAGGC A C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs921602007 Functional Loss SNV dbSNP153 33..33 33 - - - 6013 RMVar_ID_6013 Human_SNP_ID_464179592 A-to-I Human chr11 + 43857006 43857006 43857006 AAAATTAGCCAGGTGTGGTGGCACGCACCTGTAGTCCCAGCTACTTGGAAGGCTGAGGCAGGAGG AAAATTAGCCAGGTGTGGTGGCACGCACCTGTCGTCCCAGCTACTTGGAAGGCTGAGGCAGGAGG A C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs952989882 Functional Loss SNV dbSNP153 33..33 33 - - - 6014 RMVar_ID_6014 Human_SNP_ID_464180598 A-to-I Human chr11 + 43860733 43860733 43860733 GAAACTGGTCTCACTGTGTCCCCTAGGCATGTACGATGGCATGATCTTGGCTCACTGCAGCCTCA GAAACTGGTCTCACTGTGTCCCCTAGGCATGTGCGATGGCATGATCTTGGCTCACTGCAGCCTCA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1039664813 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11621039 6015 RMVar_ID_6015 Human_SNP_ID_464180626 A-to-I Human chr11 + 43860851 43860851 43860851 GTTGCCCAAGCTGGTCTGGAACTCCTGGGCTTAAATGATCCTCCGGCCTTGGCCTCCCGAAGTGT GTTGCCCAAGCTGGTCTGGAACTCCTGGGCTTGAATGATCCTCCGGCCTTGGCCTCCCGAAGTGT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1323752794 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8351519 6016 RMVar_ID_6016 Human_SNP_ID_464180645 A-to-I Human chr11 + 43860899 43860899 43860899 TTGGCCTCCCGAAGTGTTGGGATTACAGGCGTAAGCCAAGGCACCTGGCCTCTGATTGTTTTCTA TTGGCCTCCCGAAGTGTTGGGATTACAGGCGTGAGCCAAGGCACCTGGCCTCTGATTGTTTTCTA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1286908166 Functional Loss SNV dbSNP153 33..33 33 - - - 6017 RMVar_ID_6017 Human_SNP_ID_464181327 A-to-I Human chr11 + 43863875 43863875 43863875 CGCCTGCCTTGGCATCCCAAAGTGCTGGGATTATAGGTGTGAGCCACTGCACCAGGCTGGCGTTT CGCCTGCCTTGGCATCCCAAAGTGCTGGGATTGTAGGTGTGAGCCACTGCACCAGGCTGGCGTTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1020941378 Functional Loss SNV dbSNP153 33..33 33 - - - 6018 RMVar_ID_6018 Human_SNP_ID_464189399 A-to-I Human chr11 + 43898500 43898500 43898500 GGGCAGATGGACACCAACGGCTTGGTGAGAGCACTCGGGGAGGAAGCCCTGCTGAGATACGTTCT GGGCAGATGGACACCAACGGCTTGGTGAGAGCGCTCGGGGAGGAAGCCCTGCTGAGATACGTTCT A G ALKBH3,SEC14L1P1 Ensembl:ENSG00000166199,Ensembl:ENSG00000213693 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs983508147 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22522203 RMVar_hsa_circ_22093,RMVar_hsa_circ_48194,RMVar_hsa_circ_149254,RMVar_hsa_circ_93334,RMVar_hsa_circ_294653,RMVar_hsa_circ_95506,RMVar_hsa_circ_149257,RMVar_hsa_circ_75694,RMVar_hsa_circ_149259,RMVar_hsa_circ_149260,RMVar_hsa_circ_68460,RMVar_hsa_circ_357493 6019 RMVar_ID_6019 Human_SNP_ID_464189477 A-to-I Human chr11 + 43898740 43898740 43898740 AAGAGACTGGGCCGACTTCTCATCCTGCGGTCACCCAGGGTATTTCCTGTGCTCTGGACGCTGGT AAGAGACTGGGCCGACTTCTCATCCTGCGGTCGCCCAGGGTATTTCCTGTGCTCTGGACGCTGGT A G ALKBH3,SEC14L1P1 Ensembl:ENSG00000166199,Ensembl:ENSG00000213693 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1467122549 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18607863 RMVar_hsa_circ_22093,RMVar_hsa_circ_48194,RMVar_hsa_circ_149254,RMVar_hsa_circ_93334,RMVar_hsa_circ_294653,RMVar_hsa_circ_95506,RMVar_hsa_circ_149257,RMVar_hsa_circ_75694,RMVar_hsa_circ_149259,RMVar_hsa_circ_149260,RMVar_hsa_circ_68460,RMVar_hsa_circ_357493 6020 RMVar_ID_6020 Human_SNP_ID_464270693 A-to-I Human chr11 + 44247327 44247327 44247327 GGAGTGCAACAATAGCATGGTCTCGGCTCACTACATCCTCCGCCTCCCAGGTTCAAGTGATTCTC GGAGTGCAACAATAGCATGGTCTCGGCTCACTGCATCCTCCGCCTCCCAGGTTCAAGTGATTCTC A G EXT2 Ensembl:ENSG00000151348 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459874042 Functional Loss SNV dbSNP153 33..33 33 - - - 6021 RMVar_ID_6021 Human_SNP_ID_464281802 A-to-I Human chr11 - 44291687 44291687 44291687 AAATTCAATTGTTTGGCCAGGCGCAATGGCTCATGCCTGTAATCCTAGCACTTCGGGAGGCTGAG AAATTCAATTGTTTGGCCAGGCGCAATGGCTCCTGCCTGTAATCCTAGCACTTCGGGAGGCTGAG T G ALX4 Ensembl:ENSG00000052850 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1378954830 Functional Loss SNV dbSNP153 33..33 33 - - - 6022 RMVar_ID_6022 Human_SNP_ID_464281809 A-to-I Human chr11 - 44291694 44291694 44291694 GGCTAAGAAATTCAATTGTTTGGCCAGGCGCAATGGCTCATGCCTGTAATCCTAGCACTTCGGGA GGCTAAGAAATTCAATTGTTTGGCCAGGCGCAGTGGCTCATGCCTGTAATCCTAGCACTTCGGGA T C ALX4 Ensembl:ENSG00000052850 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1374776054 Functional Loss SNV dbSNP153 33..33 33 - - - 6023 RMVar_ID_6023 Human_SNP_ID_464516408 A-to-I Human chr11 + 45233234 45233234 45233234 GTGCAAAGGGGAAGGGAGCACGGCCTTCGGAGAGGGAGCCGGGGAAGGCCAGCAGGCAGGGTTGG GTGCAAAGGGGAAGGGAGCACGGCCTTCGGAGTGGGAGCCGGGGAAGGCCAGCAGGCAGGGTTGG A T PRDM11 Ensembl:ENSG00000019485 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1221875462 Functional Loss SNV dbSNP153 33..33 33 - - - 6024 RMVar_ID_6024 Human_SNP_ID_464670200 A-to-I Human chr11 + 45864940 45864938 45864941 CACAATCATGCCTGGCTAATTGTTGTCCTTTTAGTAGAGACAGGGTTTCACCCTGTTGGCCTGAC CACAATCATGCCTGGCTAATTGTTGTCCTTT___TAGAGACAGGGTTTCACCCTGTTGGCCTGAC TTAG T CRY2 Ensembl:ENSG00000121671 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1028374449 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_267601,RMVar_hsa_circ_97184,RMVar_hsa_circ_18390,RMVar_hsa_circ_149297,RMVar_hsa_circ_279591,RMVar_hsa_circ_149298 6025 RMVar_ID_6025 Human_SNP_ID_464682698 A-to-I Human chr11 - 45912436 45912436 45912436 GGAGTGTAGTGGTGCAATCTTGGCTCACTGCAAGCTCTGCCTCCCGGGTTCATGCCATTCTCCTG GGAGTGTAGTGGTGCAATCTTGGCTCACTGCACGCTCTGCCTCCCGGGTTCATGCCATTCTCCTG T G PEX16 Ensembl:ENSG00000121680 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1381711863 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_149305,RMVar_hsa_circ_116679 6026 RMVar_ID_6026 Human_SNP_ID_464682843 A-to-I Human chr11 - 45912983 45912983 45912983 CAAAAAAAAAAAAAAAATAATAATAATTAGCCAGACATGGTGGTGTGCGCCTGTAAGTCCTAGCT CAAAAAAAAAAAAAAAATAATAATAATTAGCCGGACATGGTGGTGTGCGCCTGTAAGTCCTAGCT T C PEX16 Ensembl:ENSG00000121680 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs147749008 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_149305,RMVar_hsa_circ_116679 6027 RMVar_ID_6027 Human_SNP_ID_464682891 A-to-I Human chr11 - 45913098 45913098 45913098 TGGCATAGGCTGGGCAGCAGTGGCTCACACCTATAATCCTAGCACTTTAGGAGGCCAAGGCAGGA TGGCATAGGCTGGGCAGCAGTGGCTCACACCTGTAATCCTAGCACTTTAGGAGGCCAAGGCAGGA T C PEX16 Ensembl:ENSG00000121680 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1395186680 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_149305,RMVar_hsa_circ_116679 6028 RMVar_ID_6028 Human_SNP_ID_464698795 A-to-I Human chr11 - 45974546 45974546 45974546 AGGAGAATGAGATGGGAGGATTACTTGAGCCCAGGAGGTCAAGGCTGCAGTGAGCTGTGATTACG AGGAGAATGAGATGGGAGGATTACTTGAGCCCGGGAGGTCAAGGCTGCAGTGAGCTGTGATTACG T C PHF21A Ensembl:ENSG00000135365 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1414130332 Functional Loss SNV dbSNP153 33..33 33 - - - 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 6029 RMVar_ID_6029 Human_SNP_ID_464698810 A-to-I Human chr11 - 45974614 45974614 45974614 CACGTCTCTACTAAAAATAAAAAAAATTAGCCAGGTGTGGTAGCACCTGCCTTTAGTCCAAGGTA CACGTCTCTACTAAAAATAAAAAAAATTAGCCGGGTGTGGTAGCACCTGCCTTTAGTCCAAGGTA T C PHF21A Ensembl:ENSG00000135365 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs562257784 Functional Loss SNV dbSNP153 33..33 33 - - - 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 6030 RMVar_ID_6030 Human_SNP_ID_464709526 A-to-I Human chr11 - 46022504 46022504 46022504 TTAGCCATGATCATGCCACTGCAACCTAGCCTAGGTGACAAAGGGAGACCCTGTCTTTTTGTTTC TTAGCCATGATCATGCCACTGCAACCTAGCCTCGGTGACAAAGGGAGACCCTGTCTTTTTGTTTC T G PHF21A Ensembl:ENSG00000135365 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1306208672 Functional Loss SNV dbSNP153 33..33 33 - - - 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_25414 6031 RMVar_ID_6031 Human_SNP_ID_464789142 A-to-I Human chr11 + 46359609 46359609 46359609 ACGTGGTTTTATATTTATATTTATTTATATTTATTTATTTATTTTGAGATGGAGTCTCGCTCTGT ACGTGGTTTTATATTTATATTTATTTATATTTCTTTATTTATTTTGAGATGGAGTCTCGCTCTGT A C DGKZ Ensembl:ENSG00000149091 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1565027149 Functional Loss SNV dbSNP153 33..33 33 - - - 6032 RMVar_ID_6032 Human_SNP_ID_464790447 A-to-I Human chr11 + 46364597 46364597 46364597 AAGAGCTGAGCTGTGCAGAACTCTGCTTCCCTAGGCACCTCCACCCTGTCCATCTCTCCCCCAAC AAGAGCTGAGCTGTGCAGAACTCTGCTTCCCTGGGCACCTCCACCCTGTCCATCTCTCCCCCAAC A G DGKZ Ensembl:ENSG00000149091 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1471111901 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11623966,Human_RBP_ID_17074121 6033 RMVar_ID_6033 Human_SNP_ID_464790448 A-to-I Human chr11 + 46364597 46364597 46364597 AAGAGCTGAGCTGTGCAGAACTCTGCTTCCCTAGGCACCTCCACCCTGTCCATCTCTCCCCCAAC AAGAGCTGAGCTGTGCAGAACTCTGCTTCCCTTGGCACCTCCACCCTGTCCATCTCTCCCCCAAC A T DGKZ Ensembl:ENSG00000149091 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1471111901 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11623966,Human_RBP_ID_17074121 6034 RMVar_ID_6034 Human_SNP_ID_464790734 A-to-I Human chr11 + 46365977 46365977 46365977 GCACCCACCTCCCTGGGACTCCAGGGCTCCCTAGGGTGCAATGGGGGAGAGCATCAGTGCCCCAA GCACCCACCTCCCTGGGACTCCAGGGCTCCCTCGGGTGCAATGGGGGAGAGCATCAGTGCCCCAA A C DGKZ Ensembl:ENSG00000149091 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1038898536 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_259704,Human_RBP_ID_18477668 6035 RMVar_ID_6035 Human_SNP_ID_464802611 A-to-I Human chr11 - 46404153 46404153 46404153 ACAAGATCTCGCTCTTCCATCCAGGCTGGAGTACAGTGACACGAACACGGCTCACTGCAGCCTCG ACAAGATCTCGCTCTTCCATCCAGGCTGGAGTGCAGTGACACGAACACGGCTCACTGCAGCCTCG T C AMBRA1 Ensembl:ENSG00000110497 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs903818613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6075575,Human_RBP_ID_11624061 6036 RMVar_ID_6036 Human_SNP_ID_464802909 A-to-I Human chr11 - 46405621 46405621 46405621 CCTAGGCTCAAGCGATCTTCCTGCCTCAGCCTACTGACTAGCTGGGACTACAGGTGTGTGCCACC CCTAGGCTCAAGCGATCTTCCTGCCTCAGCCTGCTGACTAGCTGGGACTACAGGTGTGTGCCACC T C AMBRA1 Ensembl:ENSG00000110497 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1386729137 Functional Loss SNV dbSNP153 33..33 33 - - - 6037 RMVar_ID_6037 Human_SNP_ID_464817709 A-to-I Human chr11 - 46469067 46469067 46469067 GTGATTTCGGCTCACTGCAACCTCCGCCTCCCAGGTTCAAGTGATTCTCCTGCCTCAGCCTCTTG GTGATTTCGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGTGATTCTCCTGCCTCAGCCTCTTG T C AMBRA1 Ensembl:ENSG00000110497 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1057452436 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25772,RMVar_hsa_circ_269632,RMVar_hsa_circ_94466,RMVar_hsa_circ_149338,RMVar_hsa_circ_39539,RMVar_hsa_circ_326618,RMVar_hsa_circ_26810,RMVar_hsa_circ_149341,RMVar_hsa_circ_339423,RMVar_hsa_circ_372836,RMVar_hsa_circ_282599,RMVar_hsa_circ_83037,RMVar_hsa_circ_3866,RMVar_hsa_circ_149342,RMVar_hsa_circ_149344,RMVar_hsa_circ_149345,RMVar_hsa_circ_149343,RMVar_hsa_circ_24087,RMVar_hsa_circ_373523,RMVar_hsa_circ_376836,RMVar_hsa_circ_36468,RMVar_hsa_circ_149348,RMVar_hsa_circ_283927,RMVar_hsa_circ_149349 6038 RMVar_ID_6038 Human_SNP_ID_464833938 A-to-I Human chr11 - 46539314 46539314 46539314 ACCTCAGGTGATCTGCCCACCTTGGCCTCCCAAAGTGCTGGGATTCCAGGTGTGAGCCACTGCGC ACCTCAGGTGATCTGCCCACCTTGGCCTCCCAGAGTGCTGGGATTCCAGGTGTGAGCCACTGCGC T C AMBRA1 Ensembl:ENSG00000110497 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs184050449 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24886373 RMVar_hsa_circ_269632,RMVar_hsa_circ_39539,RMVar_hsa_circ_26810,RMVar_hsa_circ_339423,RMVar_hsa_circ_83037,RMVar_hsa_circ_54114,RMVar_hsa_circ_149342,RMVar_hsa_circ_149343,RMVar_hsa_circ_373523,RMVar_hsa_circ_149348,RMVar_hsa_circ_283927,RMVar_hsa_circ_113499,RMVar_hsa_circ_149349,RMVar_hsa_circ_317376,RMVar_hsa_circ_376545,RMVar_hsa_circ_270037,RMVar_hsa_circ_114642,RMVar_hsa_circ_107160,RMVar_hsa_circ_90523,RMVar_hsa_circ_149353,RMVar_hsa_circ_149357,RMVar_hsa_circ_149355,RMVar_hsa_circ_149356,RMVar_hsa_circ_149354,RMVar_hsa_circ_102281,RMVar_hsa_circ_266765,RMVar_hsa_circ_149352,RMVar_hsa_circ_327985,RMVar_hsa_circ_269649,RMVar_hsa_circ_149366,RMVar_hsa_circ_265817,RMVar_hsa_circ_271697,RMVar_hsa_circ_87459,RMVar_hsa_circ_117466,RMVar_hsa_circ_149368,RMVar_hsa_circ_89360,RMVar_hsa_circ_149369,RMVar_hsa_circ_149370,RMVar_hsa_circ_149371 6039 RMVar_ID_6039 Human_SNP_ID_464836735 A-to-I Human chr11 - 46549865 46549865 46549865 GCAGTGAGCCGAGATTGCGCTGTTGCACTCCAACTGGGGCCACAGAGTGAGACTCTGTCCCCCAC GCAGTGAGCCGAGATTGCGCTGTTGCACTCCACCTGGGGCCACAGAGTGAGACTCTGTCCCCCAC T G AMBRA1 Ensembl:ENSG00000110497 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1176264598 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83037,RMVar_hsa_circ_149342,RMVar_hsa_circ_114642,RMVar_hsa_circ_149352,RMVar_hsa_circ_85092,RMVar_hsa_circ_269575,RMVar_hsa_circ_149376 6040 RMVar_ID_6040 Human_SNP_ID_464839891 A-to-I Human chr11 - 46563363 46563363 46563363 AAAATTACTGGGGCGTAGTTATATACACCTGTAGTCCCAGCTTCTGGGGAGGCCGAGATGGGAAG AAAATTACTGGGGCGTAGTTATATACACCTGTGGTCCCAGCTTCTGGGGAGGCCGAGATGGGAAG T C AMBRA1 Ensembl:ENSG00000110497 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs577499363 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22471598 RMVar_hsa_circ_83037,RMVar_hsa_circ_149342,RMVar_hsa_circ_114642,RMVar_hsa_circ_149352,RMVar_hsa_circ_85092,RMVar_hsa_circ_269575,RMVar_hsa_circ_149376 6041 RMVar_ID_6041 Human_SNP_ID_464839952 A-to-I Human chr11 - 46563648 46563648 46563648 TTTAGTAGAGACGGGGTTTCACTACATTGGCCAGGCTGGTCTCAAACTCCTGACTTCAAGTGATC TTTAGTAGAGACGGGGTTTCACTACATTGGCCCGGCTGGTCTCAAACTCCTGACTTCAAGTGATC T G AMBRA1 Ensembl:ENSG00000110497 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1414383834 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83037,RMVar_hsa_circ_149342,RMVar_hsa_circ_114642,RMVar_hsa_circ_149352,RMVar_hsa_circ_85092,RMVar_hsa_circ_269575,RMVar_hsa_circ_149376 6042 RMVar_ID_6042 Human_SNP_ID_464840369 A-to-I Human chr11 - 46565195 46565195 46565195 GGAGTGCAATGGCATAATCTCGGCTCATTGCAACCTTCGCCTCCTGGGCTCAAGTGATTTCTCCC GGAGTGCAATGGCATAATCTCGGCTCATTGCAGCCTTCGCCTCCTGGGCTCAAGTGATTTCTCCC T C AMBRA1 Ensembl:ENSG00000110497 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025264011 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83037,RMVar_hsa_circ_149342,RMVar_hsa_circ_114642,RMVar_hsa_circ_149352,RMVar_hsa_circ_85092,RMVar_hsa_circ_269575,RMVar_hsa_circ_149376 6043 RMVar_ID_6043 Human_SNP_ID_464840857 A-to-I Human chr11 - 46567119 46567119 46567119 TGCAGTAAGTCGAGATGGGACCACTGCACTCCAGTCTGGGCTACAGAGCAAGACTCTGTCTCAAA TGCAGTAAGTCGAGATGGGACCACTGCACTCCCGTCTGGGCTACAGAGCAAGACTCTGTCTCAAA T G AMBRA1 Ensembl:ENSG00000110497 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs895022864 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83037,RMVar_hsa_circ_149342,RMVar_hsa_circ_114642,RMVar_hsa_circ_149352,RMVar_hsa_circ_85092,RMVar_hsa_circ_269575,RMVar_hsa_circ_149376 6044 RMVar_ID_6044 Human_SNP_ID_464842088 A-to-I Human chr11 - 46571518 46571518 46571518 GGTATGTGCCACCATGGCTGGCTAATTTTTGTATTTTTTGTAGAGATGGGGTTTTGCCAGATTGC GGTATGTGCCACCATGGCTGGCTAATTTTTGTGTTTTTTGTAGAGATGGGGTTTTGCCAGATTGC T C AMBRA1 Ensembl:ENSG00000110497 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1248648414 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83037,RMVar_hsa_circ_149342,RMVar_hsa_circ_114642,RMVar_hsa_circ_149352,RMVar_hsa_circ_85092,RMVar_hsa_circ_269575,RMVar_hsa_circ_149376 6045 RMVar_ID_6045 Human_SNP_ID_464846198 A-to-I Human chr11 - 46586093 46586093 46586093 TTTAAAAATCATTATTATTTTCGGCTGGGTGCAGTGGCTAATGCCTGTAATCCCAGCACTTTGGG TTTAAAAATCATTATTATTTTCGGCTGGGTGCGGTGGCTAATGCCTGTAATCCCAGCACTTTGGG T C AMBRA1 Ensembl:ENSG00000110497 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1461887361 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83037,RMVar_hsa_circ_149342,RMVar_hsa_circ_114642,RMVar_hsa_circ_149352,RMVar_hsa_circ_85092,RMVar_hsa_circ_269575,RMVar_hsa_circ_149376 6046 RMVar_ID_6046 Human_SNP_ID_464847550 A-to-I Human chr11 - 46591778 46591778 46591778 ATCTCGGCTCACTGCAAACTTCTCCGCCTCCCAGGTTCAAGCAATTCTCTGCCTCAGCCTCCTGA ATCTCGGCTCACTGCAAACTTCTCCGCCTCCCGGGTTCAAGCAATTCTCTGCCTCAGCCTCCTGA T C AMBRA1 Ensembl:ENSG00000110497 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1436204459 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11626428,Human_RBP_ID_24886478 RMVar_hsa_circ_83037,RMVar_hsa_circ_149342,RMVar_hsa_circ_114642,RMVar_hsa_circ_149352,RMVar_hsa_circ_85092,RMVar_hsa_circ_269575,RMVar_hsa_circ_149376 6047 RMVar_ID_6047 Human_SNP_ID_464849769 A-to-I Human chr11 - 46599530 46599530 46599530 CTCTGACGTCAGTCTTCCGAGTAGCTGGGACTACAGGCACACACCACCATACCCAGTTAATTCTT CTCTGACGTCAGTCTTCCGAGTAGCTGGGACTGCAGGCACACACCACCATACCCAGTTAATTCTT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1426100155 Functional Loss SNV dbSNP153 33..33 33 - - - 6048 RMVar_ID_6048 Human_SNP_ID_464855548 A-to-I Human chr11 + 46620134 46620134 46620134 TTTTTTGCAATGGAGTTTCACTCTTGTTGCCCAGGCTGGAGGACAGTGGCATGATCTCGGCACAC TTTTTTGCAATGGAGTTTCACTCTTGTTGCCCGGGCTGGAGGACAGTGGCATGATCTCGGCACAC A G ATG13 Ensembl:ENSG00000175224 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs951331997 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_149380,RMVar_hsa_circ_81584 6049 RMVar_ID_6049 Human_SNP_ID_464856954 A-to-I Human chr11 + 46624851 46624851 46624851 GCGCAAGAGTTTGAGACCAGCCTGAGCAACATAGTGAGATGCTGTCTTTACAAAAAAATAAAAAA GCGCAAGAGTTTGAGACCAGCCTGAGCAACATGGTGAGATGCTGTCTTTACAAAAAAATAAAAAA A G ATG13 Ensembl:ENSG00000175224 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1012999639 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_149380,RMVar_hsa_circ_81584 6050 RMVar_ID_6050 Human_SNP_ID_464856967 A-to-I Human chr11 + 46624886 46624886 46624886 GAGATGCTGTCTTTACAAAAAAATAAAAAATTACCTGGGCATGGTGGTGTGCACCTGTAGTCCCA GAGATGCTGTCTTTACAAAAAAATAAAAAATTGCCTGGGCATGGTGGTGTGCACCTGTAGTCCCA A G ATG13 Ensembl:ENSG00000175224 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs997301264 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_149380,RMVar_hsa_circ_81584 6051 RMVar_ID_6051 Human_SNP_ID_464856968 A-to-I Human chr11 + 46624886 46624886 46624886 GAGATGCTGTCTTTACAAAAAAATAAAAAATTACCTGGGCATGGTGGTGTGCACCTGTAGTCCCA GAGATGCTGTCTTTACAAAAAAATAAAAAATTTCCTGGGCATGGTGGTGTGCACCTGTAGTCCCA A T ATG13 Ensembl:ENSG00000175224 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs997301264 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_149380,RMVar_hsa_circ_81584 6052 RMVar_ID_6052 Human_SNP_ID_464857117 A-to-I Human chr11 + 46625350 46625350 46625350 CAGGCTGGAGTGCAATGACATGATCACAGCTCACTGCAGCCATACCTCCTGGGTTCGAGTGATCT CAGGCTGGAGTGCAATGACATGATCACAGCTCCCTGCAGCCATACCTCCTGGGTTCGAGTGATCT A C ATG13 Ensembl:ENSG00000175224 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1341578479 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1233862,Human_Splice_Rec_1234050,Human_Splice_Rec_1234051 RMVar_hsa_circ_149380,RMVar_hsa_circ_81584 6053 RMVar_ID_6053 Human_SNP_ID_464860466 A-to-I Human chr11 + 46638314 46638314 46638314 CAAAAATCAGCTGGGCGAGGTGGCGCATGCCTATAATCCCAGCTACTCAGGGAGGCTGAGGCACC CAAAAATCAGCTGGGCGAGGTGGCGCATGCCTGTAATCCCAGCTACTCAGGGAGGCTGAGGCACC A G ATG13 Ensembl:ENSG00000175224 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965409141 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38317,RMVar_hsa_circ_317820,RMVar_hsa_circ_74949,RMVar_hsa_circ_111038,RMVar_hsa_circ_149381 6054 RMVar_ID_6054 Human_SNP_ID_464860608 A-to-I Human chr11 + 46638839 46638839 46638839 TTTTGTTTGTTTGTTTTTTGAGACAGAGTCTCACTCTGTCACCCAGGCTGGAGTGCAATGTTGTG TTTTGTTTGTTTGTTTTTTGAGACAGAGTCTCGCTCTGTCACCCAGGCTGGAGTGCAATGTTGTG A G ATG13 Ensembl:ENSG00000175224 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984064381 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38317,RMVar_hsa_circ_317820,RMVar_hsa_circ_74949,RMVar_hsa_circ_111038,RMVar_hsa_circ_149381 6055 RMVar_ID_6055 Human_SNP_ID_464866005 A-to-I Human chr11 + 46658639 46658639 46658639 CTCACCGCAGCCTTCACCTCTTGGGTTCAAACAGTTCTCCTGCCTGAGCCTCCCGAGTAGCTGGG CTCACCGCAGCCTTCACCTCTTGGGTTCAAACTGTTCTCCTGCCTGAGCCTCCCGAGTAGCTGGG A T ATG13 Ensembl:ENSG00000175224 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs943150323 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38317,RMVar_hsa_circ_317820,RMVar_hsa_circ_111038,RMVar_hsa_circ_358090,RMVar_hsa_circ_149381,RMVar_hsa_circ_36012,RMVar_hsa_circ_75975,RMVar_hsa_circ_124904,RMVar_hsa_circ_337819,RMVar_hsa_circ_149385,RMVar_hsa_circ_149386 6056 RMVar_ID_6056 Human_SNP_ID_464872844 A-to-I Human chr11 - 46683242 46683242 46683242 GGCCAGGAACTCAAGACCAGCCTGGGCAACATAGTGAGACCTGTCTCTACAAAATAAAAAGTAGA GGCCAGGAACTCAAGACCAGCCTGGGCAACATGGTGAGACCTGTCTCTACAAAATAAAAAGTAGA T C ARHGAP1 Ensembl:ENSG00000175220 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs549735926 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99639,RMVar_hsa_circ_120451,RMVar_hsa_circ_149395,RMVar_hsa_circ_149397,RMVar_hsa_circ_87347,RMVar_hsa_circ_149396,RMVar_hsa_circ_118713,RMVar_hsa_circ_368866,RMVar_hsa_circ_149399,RMVar_hsa_circ_120970,RMVar_hsa_circ_149402,RMVar_hsa_circ_96305,RMVar_hsa_circ_149403 6057 RMVar_ID_6057 Human_SNP_ID_464874101 A-to-I Human chr11 - 46688681 46688681 46688681 GCCAGGAGCTCAAGACCCAGCCATGGCAAGATAGTGAGATCTGTCTCTACAAAAAATTTTAAAAT GCCAGGAGCTCAAGACCCAGCCATGGCAAGATGGTGAGATCTGTCTCTACAAAAAATTTTAAAAT T C ARHGAP1 Ensembl:ENSG00000175220 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs573257636 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99639,RMVar_hsa_circ_120451,RMVar_hsa_circ_149395,RMVar_hsa_circ_149397,RMVar_hsa_circ_87347,RMVar_hsa_circ_149396,RMVar_hsa_circ_118713,RMVar_hsa_circ_368866,RMVar_hsa_circ_149399,RMVar_hsa_circ_88973,RMVar_hsa_circ_120970,RMVar_hsa_circ_149403,RMVar_hsa_circ_299843,RMVar_hsa_circ_149404 6058 RMVar_ID_6058 Human_SNP_ID_464891642 A-to-I Human chr11 - 46754981 46754981 46754981 GATCAGTTTCTGATAGCCACTTTTATGCAGCTAAGACTCATCTACAACACACACATGGCAGATGA GATCAGTTTCTGATAGCCACTTTTATGCAGCTGAGACTCATCTACAACACACACATGGCAGATGA T C CKAP5 Ensembl:ENSG00000175216 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs925589298 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_31563,Human_RBP_ID_396862,Human_RBP_ID_17234020 Human_Splice_Rec_1234470,Human_Splice_Rec_1234471,Human_Splice_Rec_1234672,Human_Splice_Rec_1234673,Human_Splice_Rec_1234704,Human_Splice_Rec_1234705,Human_Splice_Rec_1234714,Human_Splice_Rec_1234715 Human_miRNA_ID_2947454 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 6059 RMVar_ID_6059 Human_SNP_ID_464895104 A-to-I Human chr11 - 46769547 46769547 46769547 GGACTACAGGCATGCGCCATCACACCTGGCTAAATTTTTTACTTTTTATAGAGATGAGGTTTTGT GGACTACAGGCATGCGCCATCACACCTGGCTACATTTTTTACTTTTTATAGAGATGAGGTTTTGT T G CKAP5 Ensembl:ENSG00000175216 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1180339961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18608151,Human_RBP_ID_24886733 RMVar_hsa_circ_429,RMVar_hsa_circ_1052,RMVar_hsa_circ_24301,RMVar_hsa_circ_23336,RMVar_hsa_circ_288220,RMVar_hsa_circ_4657,RMVar_hsa_circ_149424,RMVar_hsa_circ_82769,RMVar_hsa_circ_265498,RMVar_hsa_circ_21691,RMVar_hsa_circ_149425,RMVar_hsa_circ_49487,RMVar_hsa_circ_103312,RMVar_hsa_circ_344999,RMVar_hsa_circ_24518,RMVar_hsa_circ_4107,RMVar_hsa_circ_27850,RMVar_hsa_circ_99847,RMVar_hsa_circ_149433,RMVar_hsa_circ_349937,RMVar_hsa_circ_69163,RMVar_hsa_circ_15860,RMVar_hsa_circ_149434 6060 RMVar_ID_6060 Human_SNP_ID_464898604 A-to-I Human chr11 - 46784285 46784285 46784285 AATCTCGGCTCACTGCAACCCTCCCGGGTTCAAGTGATTCTCCTGCTTCAGCCTCCCGCATAGCT AATCTCGGCTCACTGCAACCCTCCCGGGTTCAGGTGATTCTCCTGCTTCAGCCTCCCGCATAGCT T C CKAP5 Ensembl:ENSG00000175216 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1291569376 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_429,RMVar_hsa_circ_24301,RMVar_hsa_circ_288220,RMVar_hsa_circ_149424,RMVar_hsa_circ_82769,RMVar_hsa_circ_265498,RMVar_hsa_circ_149425,RMVar_hsa_circ_344999,RMVar_hsa_circ_4527,RMVar_hsa_circ_4107,RMVar_hsa_circ_27850,RMVar_hsa_circ_349937,RMVar_hsa_circ_69163,RMVar_hsa_circ_15860,RMVar_hsa_circ_273463,RMVar_hsa_circ_149437,RMVar_hsa_circ_102661,RMVar_hsa_circ_149438,RMVar_hsa_circ_376367,RMVar_hsa_circ_292146,RMVar_hsa_circ_329211,RMVar_hsa_circ_21282,RMVar_hsa_circ_9489,RMVar_hsa_circ_10949,RMVar_hsa_circ_149439,RMVar_hsa_circ_149440,RMVar_hsa_circ_39137,RMVar_hsa_circ_98735,RMVar_hsa_circ_149442,RMVar_hsa_circ_274162,RMVar_hsa_circ_334842,RMVar_hsa_circ_339610,RMVar_hsa_circ_39382,RMVar_hsa_circ_117759,RMVar_hsa_circ_149446,RMVar_hsa_circ_149447,RMVar_hsa_circ_149445,RMVar_hsa_circ_149449,RMVar_hsa_circ_272360,RMVar_hsa_circ_312680,RMVar_hsa_circ_357143,RMVar_hsa_circ_363341,RMVar_hsa_circ_309573,RMVar_hsa_circ_7833,RMVar_hsa_circ_81884,RMVar_hsa_circ_149451,RMVar_hsa_circ_149452,RMVar_hsa_circ_149450,RMVar_hsa_circ_149448 6061 RMVar_ID_6061 Human_SNP_ID_464898621 A-to-I Human chr11 - 46784324 46784324 46784324 GAGTTTCACTCTGTCGCCCAGGCTGGAATGCAATGGTGCAATCTCGGCTCACTGCAACCCTCCCG GAGTTTCACTCTGTCGCCCAGGCTGGAATGCATTGGTGCAATCTCGGCTCACTGCAACCCTCCCG T A CKAP5 Ensembl:ENSG00000175216 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs571380414 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_429,RMVar_hsa_circ_24301,RMVar_hsa_circ_288220,RMVar_hsa_circ_149424,RMVar_hsa_circ_82769,RMVar_hsa_circ_265498,RMVar_hsa_circ_149425,RMVar_hsa_circ_344999,RMVar_hsa_circ_4527,RMVar_hsa_circ_4107,RMVar_hsa_circ_27850,RMVar_hsa_circ_349937,RMVar_hsa_circ_69163,RMVar_hsa_circ_15860,RMVar_hsa_circ_273463,RMVar_hsa_circ_149437,RMVar_hsa_circ_102661,RMVar_hsa_circ_149438,RMVar_hsa_circ_376367,RMVar_hsa_circ_292146,RMVar_hsa_circ_329211,RMVar_hsa_circ_21282,RMVar_hsa_circ_9489,RMVar_hsa_circ_10949,RMVar_hsa_circ_149439,RMVar_hsa_circ_149440,RMVar_hsa_circ_39137,RMVar_hsa_circ_98735,RMVar_hsa_circ_149442,RMVar_hsa_circ_274162,RMVar_hsa_circ_334842,RMVar_hsa_circ_339610,RMVar_hsa_circ_39382,RMVar_hsa_circ_117759,RMVar_hsa_circ_149446,RMVar_hsa_circ_149447,RMVar_hsa_circ_149445,RMVar_hsa_circ_149449,RMVar_hsa_circ_272360,RMVar_hsa_circ_312680,RMVar_hsa_circ_357143,RMVar_hsa_circ_363341,RMVar_hsa_circ_309573,RMVar_hsa_circ_7833,RMVar_hsa_circ_81884,RMVar_hsa_circ_149451,RMVar_hsa_circ_149452,RMVar_hsa_circ_149450,RMVar_hsa_circ_149448 6062 RMVar_ID_6062 Human_SNP_ID_464898622 A-to-I Human chr11 - 46784324 46784324 46784324 GAGTTTCACTCTGTCGCCCAGGCTGGAATGCAATGGTGCAATCTCGGCTCACTGCAACCCTCCCG GAGTTTCACTCTGTCGCCCAGGCTGGAATGCAGTGGTGCAATCTCGGCTCACTGCAACCCTCCCG T C CKAP5 Ensembl:ENSG00000175216 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs571380414 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_429,RMVar_hsa_circ_24301,RMVar_hsa_circ_288220,RMVar_hsa_circ_149424,RMVar_hsa_circ_82769,RMVar_hsa_circ_265498,RMVar_hsa_circ_149425,RMVar_hsa_circ_344999,RMVar_hsa_circ_4527,RMVar_hsa_circ_4107,RMVar_hsa_circ_27850,RMVar_hsa_circ_349937,RMVar_hsa_circ_69163,RMVar_hsa_circ_15860,RMVar_hsa_circ_273463,RMVar_hsa_circ_149437,RMVar_hsa_circ_102661,RMVar_hsa_circ_149438,RMVar_hsa_circ_376367,RMVar_hsa_circ_292146,RMVar_hsa_circ_329211,RMVar_hsa_circ_21282,RMVar_hsa_circ_9489,RMVar_hsa_circ_10949,RMVar_hsa_circ_149439,RMVar_hsa_circ_149440,RMVar_hsa_circ_39137,RMVar_hsa_circ_98735,RMVar_hsa_circ_149442,RMVar_hsa_circ_274162,RMVar_hsa_circ_334842,RMVar_hsa_circ_339610,RMVar_hsa_circ_39382,RMVar_hsa_circ_117759,RMVar_hsa_circ_149446,RMVar_hsa_circ_149447,RMVar_hsa_circ_149445,RMVar_hsa_circ_149449,RMVar_hsa_circ_272360,RMVar_hsa_circ_312680,RMVar_hsa_circ_357143,RMVar_hsa_circ_363341,RMVar_hsa_circ_309573,RMVar_hsa_circ_7833,RMVar_hsa_circ_81884,RMVar_hsa_circ_149451,RMVar_hsa_circ_149452,RMVar_hsa_circ_149450,RMVar_hsa_circ_149448 6063 RMVar_ID_6063 Human_SNP_ID_464900486 A-to-I Human chr11 - 46792350 46792350 46792350 TGAGATTTCACCATGTCGTCCAGCCTGGTCTCAAACTCCTGACCTCAAATTATCTGCCTGCCTCA TGAGATTTCACCATGTCGTCCAGCCTGGTCTCCAACTCCTGACCTCAAATTATCTGCCTGCCTCA T G CKAP5 Ensembl:ENSG00000175216 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348582101 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11627991 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 6064 RMVar_ID_6064 Human_SNP_ID_464903200 A-to-I Human chr11 - 46803376 46803376 46803376 TAGTCCCAGCCAGTCGGGAGGCTGAGGTGGGAAGATCGCTTGAACCTGGGAGGGGGAGGTTGCGG TAGTCCCAGCCAGTCGGGAGGCTGAGGTGGGAGGATCGCTTGAACCTGGGAGGGGGAGGTTGCGG T C CKAP5 Ensembl:ENSG00000175216 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs930753753 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4527,RMVar_hsa_circ_15860,RMVar_hsa_circ_10949,RMVar_hsa_circ_98735,RMVar_hsa_circ_149442,RMVar_hsa_circ_39382,RMVar_hsa_circ_4397,RMVar_hsa_circ_51065,RMVar_hsa_circ_81884,RMVar_hsa_circ_149452,RMVar_hsa_circ_60445,RMVar_hsa_circ_355600,RMVar_hsa_circ_51687,RMVar_hsa_circ_303570,RMVar_hsa_circ_41637,RMVar_hsa_circ_272556,RMVar_hsa_circ_306702,RMVar_hsa_circ_69991,RMVar_hsa_circ_149459,RMVar_hsa_circ_288842,RMVar_hsa_circ_149460,RMVar_hsa_circ_298263,RMVar_hsa_circ_351505 6065 RMVar_ID_6065 Human_SNP_ID_464903211 A-to-I Human chr11 - 46803407 46803407 46803407 AAACATTAGCAGGTGTGGTAGCATGTGCCTTTAGTCCCAGCCAGTCGGGAGGCTGAGGTGGGAAG AAACATTAGCAGGTGTGGTAGCATGTGCCTTTCGTCCCAGCCAGTCGGGAGGCTGAGGTGGGAAG T G CKAP5 Ensembl:ENSG00000175216 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1186050952 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4527,RMVar_hsa_circ_15860,RMVar_hsa_circ_10949,RMVar_hsa_circ_98735,RMVar_hsa_circ_149442,RMVar_hsa_circ_39382,RMVar_hsa_circ_4397,RMVar_hsa_circ_51065,RMVar_hsa_circ_81884,RMVar_hsa_circ_149452,RMVar_hsa_circ_60445,RMVar_hsa_circ_355600,RMVar_hsa_circ_51687,RMVar_hsa_circ_303570,RMVar_hsa_circ_41637,RMVar_hsa_circ_272556,RMVar_hsa_circ_306702,RMVar_hsa_circ_69991,RMVar_hsa_circ_149459,RMVar_hsa_circ_288842,RMVar_hsa_circ_149460,RMVar_hsa_circ_298263,RMVar_hsa_circ_351505 6066 RMVar_ID_6066 Human_SNP_ID_464909880 A-to-I Human chr11 - 46831667 46831667 46831667 AATTAGACAGATGTGGTGGTGCATGCCCCAGTAGTCCTAGCTACTCAGGAGGCTGAGGCAGGAGG AATTAGACAGATGTGGTGGTGCATGCCCCAGTGGTCCTAGCTACTCAGGAGGCTGAGGCAGGAGG T C CKAP5 Ensembl:ENSG00000175216 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs963885252 Functional Loss SNV dbSNP153 33..33 33 - - - 6067 RMVar_ID_6067 Human_SNP_ID_464909883 A-to-I Human chr11 - 46831695 46831695 46831695 AGACCCTGTCTCTACAAAAAAATTTAAAAATTAGACAGATGTGGTGGTGCATGCCCCAGTAGTCC AGACCCTGTCTCTACAAAAAAATTTAAAAATTGGACAGATGTGGTGGTGCATGCCCCAGTAGTCC T C CKAP5 Ensembl:ENSG00000175216 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432903560 Functional Loss SNV dbSNP153 33..33 33 - - - 6068 RMVar_ID_6068 Human_SNP_ID_464960321 A-to-I Human chr11 + 47053919 47053919 47053919 GTGAGTCATGATTATGCCACTGACTCTAGCCTAGGTGACAGCGAGATCCTGCTTCAAAAAAACAA GTGAGTCATGATTATGCCACTGACTCTAGCCTGGGTGACAGCGAGATCCTGCTTCAAAAAAACAA A G C11orf49 Ensembl:ENSG00000149179 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256223723 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126219,RMVar_hsa_circ_109485,RMVar_hsa_circ_149475,RMVar_hsa_circ_149477,RMVar_hsa_circ_115318,RMVar_hsa_circ_149476 6069 RMVar_ID_6069 Human_SNP_ID_464964756 A-to-I Human chr11 + 47075241 47075241 47075241 TAAAACTACAAAAATTAGCCAGGTGTGATGGCAGATGTCTGTAGTCCCAGCTACTTGGGACTTGA TAAAACTACAAAAATTAGCCAGGTGTGATGGCGGATGTCTGTAGTCCCAGCTACTTGGGACTTGA A G C11orf49 Ensembl:ENSG00000149179 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1471799643 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126219,RMVar_hsa_circ_109485,RMVar_hsa_circ_149475,RMVar_hsa_circ_149477,RMVar_hsa_circ_115318,RMVar_hsa_circ_149476 6070 RMVar_ID_6070 Human_SNP_ID_464974562 A-to-I Human chr11 + 47121616 47121616 47121616 TAGCAATTGATTATTATCTCTTTTTTACAGACAAAGAAATTGATCCCTAAGTGTAAGTAGCTTGT TAGCAATTGATTATTATCTCTTTTTTACAGACGAAGAAATTGATCCCTAAGTGTAAGTAGCTTGT A G C11orf49 Ensembl:ENSG00000149179 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1424444990 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126219,RMVar_hsa_circ_109485,RMVar_hsa_circ_149475,RMVar_hsa_circ_149477,RMVar_hsa_circ_115318,RMVar_hsa_circ_149476 6071 RMVar_ID_6071 Human_SNP_ID_464974613 A-to-I Human chr11 + 47121890 47121890 47121890 GCCCAGGAGTTTGAAACCAGCCTGGGCAACATAGTAAACACAGTGACATCCCTACAAAAAAAAAA GCCCAGGAGTTTGAAACCAGCCTGGGCAACATGGTAAACACAGTGACATCCCTACAAAAAAAAAA A G C11orf49 Ensembl:ENSG00000149179 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1217985161 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126219,RMVar_hsa_circ_109485,RMVar_hsa_circ_149475,RMVar_hsa_circ_149477,RMVar_hsa_circ_115318,RMVar_hsa_circ_149476 6072 RMVar_ID_6072 Human_SNP_ID_464984085 A-to-I Human chr11 - 47163115 47163115 47163115 CAGACGGGAGTGCAGTGGCACGATCATGGCTCACTGCAGCCTCAACCTCCTGGGTTCAAGTGATC CAGACGGGAGTGCAGTGGCACGATCATGGCTCCCTGCAGCCTCAACCTCCTGGGTTCAAGTGATC T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1339014538 Functional Loss SNV dbSNP153 33..33 33 - - - 6073 RMVar_ID_6073 Human_SNP_ID_464985838 A-to-I Human chr11 - 47168573 47168573 47168573 GTGGTTGCAGTGAGCCAAGATTGCACCACTGGACTCCAGCCTGGGCGACAGAGTGAGAATCTGTC GTGGTTGCAGTGAGCCAAGATTGCACCACTGGGCTCCAGCCTGGGCGACAGAGTGAGAATCTGTC T C ARFGAP2,AC090589.3 Ensembl:ENSG00000149182,Ensembl:ENSG00000270060 Protein coding,lincRNA intron,exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1291823084 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1235438 RMVar_hsa_circ_101647,RMVar_hsa_circ_34157,RMVar_hsa_circ_74477,RMVar_hsa_circ_84663,RMVar_hsa_circ_149483,RMVar_hsa_circ_149484 6074 RMVar_ID_6074 Human_SNP_ID_464985843 A-to-I Human chr11 - 47168597 47168597 47168597 AGAATCGCTTGAACCTGGGAGGTGGTGGTTGCAGTGAGCCAAGATTGCACCACTGGACTCCAGCC AGAATCGCTTGAACCTGGGAGGTGGTGGTTGCGGTGAGCCAAGATTGCACCACTGGACTCCAGCC T C ARFGAP2,AC090589.3 Ensembl:ENSG00000149182,Ensembl:ENSG00000270060 Protein coding,lincRNA intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1315382802 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101647,RMVar_hsa_circ_34157,RMVar_hsa_circ_74477,RMVar_hsa_circ_84663,RMVar_hsa_circ_149483,RMVar_hsa_circ_149484 6075 RMVar_ID_6075 Human_SNP_ID_464985872 A-to-I Human chr11 - 47168688 47168686 47168689 CGAAACCCTGTCTCTACTGAAAAAACACAAAAAATCAGCTGGGTGTGGTGACGTGCACTGTAGTC CGAAACCCTGTCTCTACTGAAAAAACACAAA___TCAGCTGGGTGTGGTGACGTGCACTGTAGTC ATTT A ARFGAP2,AC090589.3 Ensembl:ENSG00000149182,Ensembl:ENSG00000270060 Protein coding,lincRNA intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs929230445 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_17796556 RMVar_hsa_circ_101647,RMVar_hsa_circ_34157,RMVar_hsa_circ_74477,RMVar_hsa_circ_84663,RMVar_hsa_circ_149483,RMVar_hsa_circ_149484 6076 RMVar_ID_6076 Human_SNP_ID_464985874 A-to-I Human chr11 - 47168687 47168687 47168687 GAAACCCTGTCTCTACTGAAAAAACACAAAAAATCAGCTGGGTGTGGTGACGTGCACTGTAGTCC GAAACCCTGTCTCTACTGAAAAAACACAAAAATTCAGCTGGGTGTGGTGACGTGCACTGTAGTCC T A ARFGAP2,AC090589.3 Ensembl:ENSG00000149182,Ensembl:ENSG00000270060 Protein coding,lincRNA intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1255310093 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17796556 RMVar_hsa_circ_101647,RMVar_hsa_circ_34157,RMVar_hsa_circ_74477,RMVar_hsa_circ_84663,RMVar_hsa_circ_149483,RMVar_hsa_circ_149484 6077 RMVar_ID_6077 Human_SNP_ID_464985875 A-to-I Human chr11 - 47168687 47168687 47168687 GAAACCCTGTCTCTACTGAAAAAACACAAAAAATCAGCTGGGTGTGGTGACGTGCACTGTAGTCC GAAACCCTGTCTCTACTGAAAAAACACAAAAAGTCAGCTGGGTGTGGTGACGTGCACTGTAGTCC T C ARFGAP2,AC090589.3 Ensembl:ENSG00000149182,Ensembl:ENSG00000270060 Protein coding,lincRNA intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1255310093 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17796556 RMVar_hsa_circ_101647,RMVar_hsa_circ_34157,RMVar_hsa_circ_74477,RMVar_hsa_circ_84663,RMVar_hsa_circ_149483,RMVar_hsa_circ_149484 6078 RMVar_ID_6078 Human_SNP_ID_464986155 A-to-I Human chr11 - 47169766 47169766 47169766 GCTGGAGTGCAATGGTGTGATCTCAGCTCACCACAACCTCCGCCTCCGGGGTTCAAGCTATTCTC GCTGGAGTGCAATGGTGTGATCTCAGCTCACCGCAACCTCCGCCTCCGGGGTTCAAGCTATTCTC T C ARFGAP2 Ensembl:ENSG00000149182 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1259879927 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101647,RMVar_hsa_circ_34157,RMVar_hsa_circ_74477,RMVar_hsa_circ_84663,RMVar_hsa_circ_149483,RMVar_hsa_circ_149484 6079 RMVar_ID_6079 Human_SNP_ID_464986248 A-to-I Human chr11 - 47170145 47170145 47170145 TTATTTTTGTATTTTAGTAGAGATGGGGTTTCACCATGTTGCCCAGGCTGGTGTAAAACTACTAG TTATTTTTGTATTTTAGTAGAGATGGGGTTTCCCCATGTTGCCCAGGCTGGTGTAAAACTACTAG T G ARFGAP2 Ensembl:ENSG00000149182 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1309869033 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11631224 RMVar_hsa_circ_101647,RMVar_hsa_circ_34157,RMVar_hsa_circ_74477,RMVar_hsa_circ_84663,RMVar_hsa_circ_149483,RMVar_hsa_circ_149484 6080 RMVar_ID_6080 Human_SNP_ID_464986265 A-to-I Human chr11 - 47170238 47170227 47170238 CCCACTGCAGCCTCCGCCTCCCAGATTCAAGCAATTCTCCTGCCTCAGCCTCCTGAGAAGCTGTG CCCACTGCAGCCTCCGCCTCCCAGATTCAAGC___________CTCAGCCTCCTGAGAAGCTGTG GGCAGGAGAATT G ARFGAP2 Ensembl:ENSG00000149182 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs980516930 Functional Loss DEL dbSNP153 33..43 33 - - - RMVar_hsa_circ_101647,RMVar_hsa_circ_34157,RMVar_hsa_circ_74477,RMVar_hsa_circ_84663,RMVar_hsa_circ_149483,RMVar_hsa_circ_149484 6081 RMVar_ID_6081 Human_SNP_ID_464986279 A-to-I Human chr11 - 47170267 47170267 47170267 CAGGCTGGAGTTCAGTGGTGTGATCTCAGCCCACTGCAGCCTCCGCCTCCCAGATTCAAGCAATT CAGGCTGGAGTTCAGTGGTGTGATCTCAGCCCGCTGCAGCCTCCGCCTCCCAGATTCAAGCAATT T C ARFGAP2 Ensembl:ENSG00000149182 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1362469542 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11631225 RMVar_hsa_circ_101647,RMVar_hsa_circ_34157,RMVar_hsa_circ_74477,RMVar_hsa_circ_84663,RMVar_hsa_circ_149483,RMVar_hsa_circ_149484 6082 RMVar_ID_6082 Human_SNP_ID_464986411 A-to-I Human chr11 - 47170707 47170707 47170707 TCCTGGGTTTAAGTACCTTGGCTTCACAAAGTACTGGGATTACAGATGTGAGCCACCATGTCTGG TCCTGGGTTTAAGTACCTTGGCTTCACAAAGTGCTGGGATTACAGATGTGAGCCACCATGTCTGG T C ARFGAP2 Ensembl:ENSG00000149182 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs754235613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1264725 RMVar_hsa_circ_101647,RMVar_hsa_circ_34157,RMVar_hsa_circ_74477,RMVar_hsa_circ_84663,RMVar_hsa_circ_149483,RMVar_hsa_circ_149484 6083 RMVar_ID_6083 Human_SNP_ID_464988780 A-to-I Human chr11 - 47177768 47177768 47177768 CTGGGACCCAGGGAGGGGAGGGGCCTTTGTCTAGGGAAGGGACTGGTAGGGAAGGGACGAGTCTA CTGGGACCCAGGGAGGGGAGGGGCCTTTGTCTCGGGAAGGGACTGGTAGGGAAGGGACGAGTCTA T G PACSIN3 Ensembl:ENSG00000165912 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs941007530 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_807871,Human_RBP_ID_9352633,Human_RBP_ID_9415454,Human_RBP_ID_17649534,Human_RBP_ID_18159370,Human_RBP_ID_26408419 Human_miRNA_ID_2210446 RMVar_hsa_circ_80682,RMVar_hsa_circ_112915,RMVar_hsa_circ_82806,RMVar_hsa_circ_149490,RMVar_hsa_circ_149492,RMVar_hsa_circ_76795,RMVar_hsa_circ_149491,RMVar_hsa_circ_149489 6084 RMVar_ID_6084 Human_SNP_ID_464999054 A-to-I Human chr11 + 47217744 47217744 47217744 AAACCCCGTCTCTACTAAAGATACAAAAAATTAGCTGGATGTGGTGGTGTGCGCCTGTAGTCCCA AAACCCCGTCTCTACTAAAGATACAAAAAATTGGCTGGATGTGGTGGTGTGCGCCTGTAGTCCCA A G DDB2 Ensembl:ENSG00000134574 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs904138470 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115720,RMVar_hsa_circ_341997,RMVar_hsa_circ_312085,RMVar_hsa_circ_121105,RMVar_hsa_circ_298445,RMVar_hsa_circ_149496,RMVar_hsa_circ_149497,RMVar_hsa_circ_149499,RMVar_hsa_circ_111960,RMVar_hsa_circ_149498 6085 RMVar_ID_6085 Human_SNP_ID_464999341 A-to-I Human chr11 + 47219044 47219044 47219044 TTGGCTCACTGCAAGCTCCGCCTCCCGGATTCATGCCATTCTCCTGCCTCAGCCTCCCCAGCAGC TTGGCTCACTGCAAGCTCCGCCTCCCGGATTCGTGCCATTCTCCTGCCTCAGCCTCCCCAGCAGC A G DDB2 Ensembl:ENSG00000134574 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs909931043 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115720,RMVar_hsa_circ_341997,RMVar_hsa_circ_312085,RMVar_hsa_circ_121105,RMVar_hsa_circ_298445,RMVar_hsa_circ_149496,RMVar_hsa_circ_149497,RMVar_hsa_circ_149499,RMVar_hsa_circ_111960,RMVar_hsa_circ_149498 6086 RMVar_ID_6086 Human_SNP_ID_464999414 A-to-I Human chr11 + 47219460 47219460 47219460 ATAGCTCACTGCAGCCTCCACCTTCCTGACTCAAGGAATCCTCCGGCTTCAGCCTCCCATGTATC ATAGCTCACTGCAGCCTCCACCTTCCTGACTCCAGGAATCCTCCGGCTTCAGCCTCCCATGTATC A C DDB2 Ensembl:ENSG00000134574 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs940202532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1354428 RMVar_hsa_circ_115720,RMVar_hsa_circ_341997,RMVar_hsa_circ_312085,RMVar_hsa_circ_121105,RMVar_hsa_circ_298445,RMVar_hsa_circ_149496,RMVar_hsa_circ_149497,RMVar_hsa_circ_149499,RMVar_hsa_circ_111960,RMVar_hsa_circ_149498 6087 RMVar_ID_6087 Human_SNP_ID_464999436 A-to-I Human chr11 + 47219552 47219552 47219552 CTGGCTAATTTTTAGAGATGTGGTCTCTCTATATTGCCCAGGCTGGTCTCAAACTACTGGCCTCA CTGGCTAATTTTTAGAGATGTGGTCTCTCTATGTTGCCCAGGCTGGTCTCAAACTACTGGCCTCA A G DDB2 Ensembl:ENSG00000134574 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs557150203 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17559943 RMVar_hsa_circ_115720,RMVar_hsa_circ_341997,RMVar_hsa_circ_312085,RMVar_hsa_circ_121105,RMVar_hsa_circ_298445,RMVar_hsa_circ_149496,RMVar_hsa_circ_149497,RMVar_hsa_circ_149499,RMVar_hsa_circ_111960,RMVar_hsa_circ_149498 6088 RMVar_ID_6088 Human_SNP_ID_464999856 A-to-I Human chr11 + 47221468 47221467 47221469 CTAATTTTTGTTTTGTTTTGTTTTTTTAAGACAGAGTTTCACTCTATTGCCCAGGCTGGAGTGCA CTAATTTTTGTTTTGTTTTGTTTTTTTAAGAC__AGTTTCACTCTATTGCCCAGGCTGGAGTGCA CAG C DDB2 Ensembl:ENSG00000134574 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1035262350 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_11631577,Human_RBP_ID_23153938 RMVar_hsa_circ_115720,RMVar_hsa_circ_341997,RMVar_hsa_circ_312085,RMVar_hsa_circ_121105,RMVar_hsa_circ_298445,RMVar_hsa_circ_149496,RMVar_hsa_circ_149497,RMVar_hsa_circ_149499,RMVar_hsa_circ_111960,RMVar_hsa_circ_149498 6089 RMVar_ID_6089 Human_SNP_ID_464999861 A-to-I Human chr11 + 47221481 47221481 47221481 TGTTTTGTTTTTTTAAGACAGAGTTTCACTCTATTGCCCAGGCTGGAGTGCAGTAGCACGATCTC TGTTTTGTTTTTTTAAGACAGAGTTTCACTCTGTTGCCCAGGCTGGAGTGCAGTAGCACGATCTC A G DDB2 Ensembl:ENSG00000134574 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1246181090 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115720,RMVar_hsa_circ_341997,RMVar_hsa_circ_312085,RMVar_hsa_circ_121105,RMVar_hsa_circ_298445,RMVar_hsa_circ_149496,RMVar_hsa_circ_149497,RMVar_hsa_circ_149499,RMVar_hsa_circ_111960,RMVar_hsa_circ_149498 6090 RMVar_ID_6090 Human_SNP_ID_464999887 A-to-I Human chr11 + 47221610 47221610 47221610 GGGATTACAGGAGCCTACCACCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCA GGGATTACAGGAGCCTACCACCATGCCCAGCTGATTTTTGTATTTTTAGTAGAGACGGGGTTTCA A G DDB2 Ensembl:ENSG00000134574 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1421774470 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115720,RMVar_hsa_circ_341997,RMVar_hsa_circ_312085,RMVar_hsa_circ_121105,RMVar_hsa_circ_298445,RMVar_hsa_circ_149496,RMVar_hsa_circ_149497,RMVar_hsa_circ_149499,RMVar_hsa_circ_111960,RMVar_hsa_circ_149498 6091 RMVar_ID_6091 Human_SNP_ID_465000087 A-to-I Human chr11 + 47222526 47222526 47222526 CCACCATACCTGGCTAATTTTAAAATTTTGTTATAGAGACAGAGGTCTCACTGTGTTGCACAGGC CCACCATACCTGGCTAATTTTAAAATTTTGTTGTAGAGACAGAGGTCTCACTGTGTTGCACAGGC A G DDB2 Ensembl:ENSG00000134574 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs781493486 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115720,RMVar_hsa_circ_341997,RMVar_hsa_circ_312085,RMVar_hsa_circ_121105,RMVar_hsa_circ_298445,RMVar_hsa_circ_149496,RMVar_hsa_circ_149497,RMVar_hsa_circ_149499,RMVar_hsa_circ_111960,RMVar_hsa_circ_149498 6092 RMVar_ID_6092 Human_SNP_ID_465000211 A-to-I Human chr11 + 47223235 47223234 47223235 GGCTGGGCGCTGTGGCTTACGCCTGTAATCCCAGCATTTTGGGGGGCCAAGGCAAGTGGATCATT GGCTGGGCGCTGTGGCTTACGCCTGTAATCCC_GCATTTTGGGGGGCCAAGGCAAGTGGATCATT CA C DDB2 Ensembl:ENSG00000134574 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs767449553 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_115720,RMVar_hsa_circ_341997,RMVar_hsa_circ_312085,RMVar_hsa_circ_121105,RMVar_hsa_circ_298445,RMVar_hsa_circ_149496,RMVar_hsa_circ_149497,RMVar_hsa_circ_149499,RMVar_hsa_circ_111960,RMVar_hsa_circ_149498 6093 RMVar_ID_6093 Human_SNP_ID_465000297 A-to-I Human chr11 + 47223531 47223531 47223531 GGCTGGGCGCGGTGGCTGACACCTGTAATCCCAGCGCTTTGGGAGGCCGAGGCAGGCGGATCACG GGCTGGGCGCGGTGGCTGACACCTGTAATCCCGGCGCTTTGGGAGGCCGAGGCAGGCGGATCACG A G DDB2 Ensembl:ENSG00000134574 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs960732640 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115720,RMVar_hsa_circ_341997,RMVar_hsa_circ_312085,RMVar_hsa_circ_121105,RMVar_hsa_circ_298445,RMVar_hsa_circ_149496,RMVar_hsa_circ_149497,RMVar_hsa_circ_149499,RMVar_hsa_circ_111960,RMVar_hsa_circ_149498 6094 RMVar_ID_6094 Human_SNP_ID_465000307 A-to-I Human chr11 + 47223569 47223568 47223570 TTGGGAGGCCGAGGCAGGCGGATCACGAGATCAAGAGATTGAGACCACCCTGGCTAACACGGTGA TTGGGAGGCCGAGGCAGGCGGATCACGAGATC__GAGATTGAGACCACCCTGGCTAACACGGTGA CAA C DDB2 Ensembl:ENSG00000134574 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1461302845 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_11631609 RMVar_hsa_circ_115720,RMVar_hsa_circ_341997,RMVar_hsa_circ_312085,RMVar_hsa_circ_121105,RMVar_hsa_circ_298445,RMVar_hsa_circ_149496,RMVar_hsa_circ_149497,RMVar_hsa_circ_149499,RMVar_hsa_circ_111960,RMVar_hsa_circ_149498 6095 RMVar_ID_6095 Human_SNP_ID_465000650 A-to-I Human chr11 + 47225105 47225105 47225105 GGGATTACAAGTGTGCACCACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGACCAAGTTTCA GGGATTACAAGTGTGCACCACCACGCCCAGCTGATTTTTGTATTTTTAGTAGAGACCAAGTTTCA A G DDB2 Ensembl:ENSG00000134574 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1375852730 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115720,RMVar_hsa_circ_341997,RMVar_hsa_circ_312085,RMVar_hsa_circ_121105,RMVar_hsa_circ_298445,RMVar_hsa_circ_149496,RMVar_hsa_circ_149497,RMVar_hsa_circ_149499,RMVar_hsa_circ_111960,RMVar_hsa_circ_149498 6096 RMVar_ID_6096 Human_SNP_ID_465001081 A-to-I Human chr11 + 47226795 47226795 47226795 ACAGGGTCTTACTTGGTCACCCAGGCTGCAGTACAGTGGCACAATCATAGCTCACTGCAGCCTCG ACAGGGTCTTACTTGGTCACCCAGGCTGCAGTTCAGTGGCACAATCATAGCTCACTGCAGCCTCG A T DDB2 Ensembl:ENSG00000134574 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1232443071 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11631632 RMVar_hsa_circ_115720,RMVar_hsa_circ_341997,RMVar_hsa_circ_312085,RMVar_hsa_circ_121105,RMVar_hsa_circ_298445,RMVar_hsa_circ_149496,RMVar_hsa_circ_149497,RMVar_hsa_circ_149499,RMVar_hsa_circ_111960,RMVar_hsa_circ_149498 6097 RMVar_ID_6097 Human_SNP_ID_465001090 A-to-I Human chr11 + 47226842 47226842 47226842 TAGCTCACTGCAGCCTCGAACTTCTGGGCTCCAGTGATCCTGCTGCCTTAGCCACCCGAGTAACT TAGCTCACTGCAGCCTCGAACTTCTGGGCTCCGGTGATCCTGCTGCCTTAGCCACCCGAGTAACT A G DDB2 Ensembl:ENSG00000134574 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560943922 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11631633 RMVar_hsa_circ_115720,RMVar_hsa_circ_341997,RMVar_hsa_circ_312085,RMVar_hsa_circ_121105,RMVar_hsa_circ_298445,RMVar_hsa_circ_149496,RMVar_hsa_circ_149497,RMVar_hsa_circ_149499,RMVar_hsa_circ_111960,RMVar_hsa_circ_149498 6098 RMVar_ID_6098 Human_SNP_ID_465001098 A-to-I Human chr11 + 47226871 47226871 47226871 TCCAGTGATCCTGCTGCCTTAGCCACCCGAGTAACTGGGACTGCAGGTGCTCACCATCATACCTT TCCAGTGATCCTGCTGCCTTAGCCACCCGAGTTACTGGGACTGCAGGTGCTCACCATCATACCTT A T DDB2 Ensembl:ENSG00000134574 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1472908221 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11631633 RMVar_hsa_circ_115720,RMVar_hsa_circ_341997,RMVar_hsa_circ_312085,RMVar_hsa_circ_121105,RMVar_hsa_circ_298445,RMVar_hsa_circ_149496,RMVar_hsa_circ_149497,RMVar_hsa_circ_149499,RMVar_hsa_circ_111960,RMVar_hsa_circ_149498 6099 RMVar_ID_6099 Human_SNP_ID_465001935 A-to-I Human chr11 + 47229900 47229900 47229900 CCACCCAGGCTGGAATGCAGTGGCAGGATCATAGCTAACTACAGCCTTGAACTCCTGGGCTCAAG CCACCCAGGCTGGAATGCAGTGGCAGGATCATCGCTAACTACAGCCTTGAACTCCTGGGCTCAAG A C DDB2 Ensembl:ENSG00000134574 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs769110911 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115720,RMVar_hsa_circ_341997,RMVar_hsa_circ_312085,RMVar_hsa_circ_121105,RMVar_hsa_circ_298445,RMVar_hsa_circ_149496,RMVar_hsa_circ_149497,RMVar_hsa_circ_149499,RMVar_hsa_circ_111960,RMVar_hsa_circ_149498 6100 RMVar_ID_6100 Human_SNP_ID_465001972 A-to-I Human chr11 + 47230071 47230055 47230072 GCCTGTAACAGCACTTTGGGACGTTGAGGTGGAAGGATTGCTTGAGCCCAGGAATTTGAGACTGG GCCTGTAACAGCACTTT_________________GGATTGCTTGAGCCCAGGAATTTGAGACTGG TGGGACGTTGAGGTGGAA T DDB2 Ensembl:ENSG00000134574 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs148013513 Functional Loss DEL dbSNP153 18..34 33 - - - Human_RBP_ID_24887575 GWAS_ID_262,GWAS_ID_263,GWAS_ID_264,GWAS_ID_265,GWAS_ID_266,GWAS_ID_267,GWAS_ID_268,GWAS_ID_269,GWAS_ID_270,GWAS_ID_271,GWAS_ID_272,GWAS_ID_273,GWAS_ID_274,GWAS_ID_275,GWAS_ID_276,GWAS_ID_277,GWAS_ID_278,GWAS_ID_279,GWAS_ID_280,GWAS_ID_281,GWAS_ID_282,GWAS_ID_283,GWAS_ID_284,GWAS_ID_285,GWAS_ID_286,GWAS_ID_287,GWAS_ID_288,GWAS_ID_289 RMVar_hsa_circ_115720,RMVar_hsa_circ_341997,RMVar_hsa_circ_312085,RMVar_hsa_circ_121105,RMVar_hsa_circ_298445,RMVar_hsa_circ_149496,RMVar_hsa_circ_149497,RMVar_hsa_circ_149499,RMVar_hsa_circ_111960,RMVar_hsa_circ_149498 6101 RMVar_ID_6101 Human_SNP_ID_465002371 A-to-I Human chr11 + 47231579 47231579 47231579 AGGGTCTTGCTCTGTCACCCACGCTAGAGTGCAGTGATTCGATCGCAACTCACTGCAGCCTCGAC AGGGTCTTGCTCTGTCACCCACGCTAGAGTGCCGTGATTCGATCGCAACTCACTGCAGCCTCGAC A C DDB2 Ensembl:ENSG00000134574 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1342238518 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115720,RMVar_hsa_circ_341997,RMVar_hsa_circ_312085,RMVar_hsa_circ_121105,RMVar_hsa_circ_298445,RMVar_hsa_circ_149496,RMVar_hsa_circ_149497,RMVar_hsa_circ_149499,RMVar_hsa_circ_111960,RMVar_hsa_circ_149498 6102 RMVar_ID_6102 Human_SNP_ID_465002395 A-to-I Human chr11 + 47231662 47231662 47231662 TTCCCACCTCAGCCTTCTGAGTAGCTAGAACCACATGCACCTACCACCATGTCTAAATTTTTTTT TTCCCACCTCAGCCTTCTGAGTAGCTAGAACCCCATGCACCTACCACCATGTCTAAATTTTTTTT A C DDB2 Ensembl:ENSG00000134574 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1325202626 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115720,RMVar_hsa_circ_341997,RMVar_hsa_circ_312085,RMVar_hsa_circ_121105,RMVar_hsa_circ_298445,RMVar_hsa_circ_149496,RMVar_hsa_circ_149497,RMVar_hsa_circ_149499,RMVar_hsa_circ_111960,RMVar_hsa_circ_149498 6103 RMVar_ID_6103 Human_SNP_ID_465007618 A-to-I Human chr11 + 47251350 47251350 47251350 ACTAAACGGGACCTAGGCCGGACATGGCTCACACCTGTAATCCCAGCACTTTGGGAGGACGAGGC ACTAAACGGGACCTAGGCCGGACATGGCTCACTCCTGTAATCCCAGCACTTTGGGAGGACGAGGC A T NR1H3 Ensembl:ENSG00000025434 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006053946 Functional Loss SNV dbSNP153 33..33 33 - - - 6104 RMVar_ID_6104 Human_SNP_ID_465008140 A-to-I Human chr11 + 47253183 47253183 47253183 TAAAGGTGAGGTTTCGCCATGTTGCCTAGGCTAGTCTCAAACTCCTGGACTCAAGCGATCTGCCC TAAAGGTGAGGTTTCGCCATGTTGCCTAGGCTGGTCTCAAACTCCTGGACTCAAGCGATCTGCCC A G NR1H3 Ensembl:ENSG00000025434 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1165932851 Functional Loss SNV dbSNP153 33..33 33 - - - 6105 RMVar_ID_6105 Human_SNP_ID_465018148 A-to-I Human chr11 + 47287431 47287431 47287431 TTTGATTTTTTATTTTTTTTATTTTCTGAGACAGTGTCACTCCGTCACCCAGGCTGGATGGAGTG TTTGATTTTTTATTTTTTTTATTTTCTGAGACTGTGTCACTCCGTCACCCAGGCTGGATGGAGTG A T MADD Ensembl:ENSG00000110514 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027371800 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5168343,Human_RBP_ID_17559947 RMVar_hsa_circ_13669,RMVar_hsa_circ_359569,RMVar_hsa_circ_33334,RMVar_hsa_circ_54290,RMVar_hsa_circ_371840,RMVar_hsa_circ_149512,RMVar_hsa_circ_108152,RMVar_hsa_circ_149513,RMVar_hsa_circ_56757 6106 RMVar_ID_6106 Human_SNP_ID_465018192 A-to-I Human chr11 + 47287590 47287590 47287590 TACCACCTCGCCTGGCTAATTGTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGC TACCACCTCGCCTGGCTAATTGTTGTATTTTTGGTAGAGACGGGGTTTCACCATGTTGGCCAGGC A G MADD Ensembl:ENSG00000110514 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs562082868 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13669,RMVar_hsa_circ_359569,RMVar_hsa_circ_33334,RMVar_hsa_circ_54290,RMVar_hsa_circ_371840,RMVar_hsa_circ_149512,RMVar_hsa_circ_108152,RMVar_hsa_circ_149513,RMVar_hsa_circ_56757 6107 RMVar_ID_6107 Human_SNP_ID_465018200 A-to-I Human chr11 + 47287610 47287610 47287610 TGTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGACCT TGTTGTATTTTTAGTAGAGACGGGGTTTCACCGTGTTGGCCAGGCTGGTCTTGAACTCCTGACCT A G MADD Ensembl:ENSG00000110514 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs750318098 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13669,RMVar_hsa_circ_359569,RMVar_hsa_circ_33334,RMVar_hsa_circ_54290,RMVar_hsa_circ_371840,RMVar_hsa_circ_149512,RMVar_hsa_circ_108152,RMVar_hsa_circ_149513,RMVar_hsa_circ_56757 6108 RMVar_ID_6108 Human_SNP_ID_465018212 A-to-I Human chr11 + 47287671 47287671 47287671 ACCTTGAGTGATCTGCCCACCTTGGCCTCCCAAAGTGCCAGGATTACAGGTGTGAGCCACTGCAC ACCTTGAGTGATCTGCCCACCTTGGCCTCCCAGAGTGCCAGGATTACAGGTGTGAGCCACTGCAC A G MADD Ensembl:ENSG00000110514 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1275361281 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13669,RMVar_hsa_circ_359569,RMVar_hsa_circ_33334,RMVar_hsa_circ_54290,RMVar_hsa_circ_371840,RMVar_hsa_circ_149512,RMVar_hsa_circ_108152,RMVar_hsa_circ_149513,RMVar_hsa_circ_56757 6109 RMVar_ID_6109 Human_SNP_ID_465026654 A-to-I Human chr11 + 47319244 47319244 47319244 ACATCCACCCACCGACTTCAAGAGATTCTCCTACCTCAGACTCCCGAGTAGCTGGGACTACAGGC ACATCCACCCACCGACTTCAAGAGATTCTCCTGCCTCAGACTCCCGAGTAGCTGGGACTACAGGC A G MADD Ensembl:ENSG00000110514 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1565550683 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108152,RMVar_hsa_circ_149513,RMVar_hsa_circ_113803,RMVar_hsa_circ_149517 6110 RMVar_ID_6110 Human_SNP_ID_465041307 A-to-I Human chr11 - 47362390 47362387 47362391 TTTTTAAACATTTTTTGTAGAGATAGGGTCTCACTATGTTGCCCAGGCCGGTCTCAAACTCCTGG TTTTTAAACATTTTTTGTAGAGATAGGGTCT____ATGTTGCCCAGGCCGGTCTCAAACTCCTGG TAGTG T SPI1 Ensembl:ENSG00000066336 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1435091157 Functional Loss DEL dbSNP153 32..35 33 - - - RMVar_hsa_circ_149524,RMVar_hsa_circ_304539,RMVar_hsa_circ_298672,RMVar_hsa_circ_149525,RMVar_hsa_circ_372617 6111 RMVar_ID_6111 Human_SNP_ID_465041308 A-to-I Human chr11 - 47362390 47362390 47362390 TTTTTAAACATTTTTTGTAGAGATAGGGTCTCACTATGTTGCCCAGGCCGGTCTCAAACTCCTGG TTTTTAAACATTTTTTGTAGAGATAGGGTCTCCCTATGTTGCCCAGGCCGGTCTCAAACTCCTGG T G SPI1 Ensembl:ENSG00000066336 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1047825162 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_149524,RMVar_hsa_circ_304539,RMVar_hsa_circ_298672,RMVar_hsa_circ_149525,RMVar_hsa_circ_372617 6112 RMVar_ID_6112 Human_SNP_ID_465042743 A-to-I Human chr11 - 47367960 47367960 47367960 TCACAAGGTCAAGAGATTGAGACCTGGCTAACATGGTGAAACCCCATCTCTACTAAAAATACAAA TCACAAGGTCAAGAGATTGAGACCTGGCTAACGTGGTGAAACCCCATCTCTACTAAAAATACAAA T C SPI1 Ensembl:ENSG00000066336 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs966572181 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_149524,RMVar_hsa_circ_304539,RMVar_hsa_circ_298672,RMVar_hsa_circ_149525,RMVar_hsa_circ_372617 6113 RMVar_ID_6113 Human_SNP_ID_465044167 A-to-I Human chr11 - 47373547 47373547 47373547 GCCTCCTGGGTCCAAGCGATTCTCTTGCCTCAACATCCCAAGTAGCTAGGATTACAATCGTGCAC GCCTCCTGGGTCCAAGCGATTCTCTTGCCTCAGCATCCCAAGTAGCTAGGATTACAATCGTGCAC T C SPI1 Ensembl:ENSG00000066336 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1271645222 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_149524,RMVar_hsa_circ_304539,RMVar_hsa_circ_298672,RMVar_hsa_circ_149525,RMVar_hsa_circ_372617 6114 RMVar_ID_6114 Human_SNP_ID_465056985 A-to-I Human chr11 - 47421791 47421791 47421791 AAAATTAGCCGGGTGTGGTGGTGTGCGCCTGTAATTCCAGCTACTTGGGAGGCTGAGGCAGGAGA AAAATTAGCCGGGTGTGGTGGTGTGCGCCTGTCATTCCAGCTACTTGGGAGGCTGAGGCAGGAGA T G PSMC3 Ensembl:ENSG00000165916 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1345116368 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107277,RMVar_hsa_circ_124811,RMVar_hsa_circ_114541,RMVar_hsa_circ_149534,RMVar_hsa_circ_95983,RMVar_hsa_circ_102948,RMVar_hsa_circ_105397,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_149535,RMVar_hsa_circ_102589,RMVar_hsa_circ_125693,RMVar_hsa_circ_149541,RMVar_hsa_circ_149542 6115 RMVar_ID_6115 Human_SNP_ID_465057014 A-to-I Human chr11 - 47421875 47421875 47421875 GGCTGAGGTGGGCAGATCACTTGAGGTCAGGAATTCGAGACCAGCCTGGCCAACATGGTGAAACA GGCTGAGGTGGGCAGATCACTTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACA T C PSMC3 Ensembl:ENSG00000165916 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs997896994 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24887827 RMVar_hsa_circ_107277,RMVar_hsa_circ_124811,RMVar_hsa_circ_114541,RMVar_hsa_circ_149534,RMVar_hsa_circ_95983,RMVar_hsa_circ_102948,RMVar_hsa_circ_105397,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_149535,RMVar_hsa_circ_102589,RMVar_hsa_circ_125693,RMVar_hsa_circ_149541,RMVar_hsa_circ_149542 6116 RMVar_ID_6116 Human_SNP_ID_465057093 A-to-I Human chr11 - 47422194 47422194 47422194 ACTAAAAATACAAAAAATTAGCTGGGCGTGGTAGCAGGCGCCTGTAGTCCCAGATGCCTGGGAGG ACTAAAAATACAAAAAATTAGCTGGGCGTGGTTGCAGGCGCCTGTAGTCCCAGATGCCTGGGAGG T A PSMC3 Ensembl:ENSG00000165916 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1038911611 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_109452 RMVar_hsa_circ_107277,RMVar_hsa_circ_124811,RMVar_hsa_circ_114541,RMVar_hsa_circ_149534,RMVar_hsa_circ_95983,RMVar_hsa_circ_102948,RMVar_hsa_circ_105397,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_149535,RMVar_hsa_circ_102589,RMVar_hsa_circ_125693,RMVar_hsa_circ_149541,RMVar_hsa_circ_149542 6117 RMVar_ID_6117 Human_SNP_ID_465072408 A-to-I Human chr11 - 47480260 47480260 47480260 CAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCTGGGTGTGATGGTACACACCT CAACATGGTGAAACCCCGTCTCTACTAAAAATGCAAAAATTAGCTGGGTGTGATGGTACACACCT T C CELF1 Ensembl:ENSG00000149187 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs545999540 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119120,RMVar_hsa_circ_37929,RMVar_hsa_circ_149551,RMVar_hsa_circ_288701,RMVar_hsa_circ_375912,RMVar_hsa_circ_332850,RMVar_hsa_circ_19919,RMVar_hsa_circ_35187,RMVar_hsa_circ_5549,RMVar_hsa_circ_19207,RMVar_hsa_circ_149553,RMVar_hsa_circ_149554,RMVar_hsa_circ_75150,RMVar_hsa_circ_149555,RMVar_hsa_circ_11194,RMVar_hsa_circ_295519,RMVar_hsa_circ_361828,RMVar_hsa_circ_348304,RMVar_hsa_circ_149556,RMVar_hsa_circ_283690,RMVar_hsa_circ_318259,RMVar_hsa_circ_341549,RMVar_hsa_circ_36084,RMVar_hsa_circ_149559,RMVar_hsa_circ_149560,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 6118 RMVar_ID_6118 Human_SNP_ID_465072555 A-to-I Human chr11 - 47480888 47480888 47480888 GGGATTACAGTCATGTGCCACCACGCCTGGCTAATTTTTGTAGTTTTAGTAGAGACAGGGTTTTG GGGATTACAGTCATGTGCCACCACGCCTGGCTGATTTTTGTAGTTTTAGTAGAGACAGGGTTTTG T C CELF1 Ensembl:ENSG00000149187 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs535361936 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11633877 RMVar_hsa_circ_119120,RMVar_hsa_circ_37929,RMVar_hsa_circ_149551,RMVar_hsa_circ_288701,RMVar_hsa_circ_375912,RMVar_hsa_circ_332850,RMVar_hsa_circ_19919,RMVar_hsa_circ_35187,RMVar_hsa_circ_5549,RMVar_hsa_circ_19207,RMVar_hsa_circ_149553,RMVar_hsa_circ_149554,RMVar_hsa_circ_75150,RMVar_hsa_circ_149555,RMVar_hsa_circ_11194,RMVar_hsa_circ_295519,RMVar_hsa_circ_361828,RMVar_hsa_circ_348304,RMVar_hsa_circ_149556,RMVar_hsa_circ_283690,RMVar_hsa_circ_318259,RMVar_hsa_circ_341549,RMVar_hsa_circ_36084,RMVar_hsa_circ_149559,RMVar_hsa_circ_149560,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 6119 RMVar_ID_6119 Human_SNP_ID_465072566 A-to-I Human chr11 - 47480924 47480924 47480924 ATCTCTGCTCACTGCAACCTCCAACTGCAAGCAGCTGGGATTACAGTCATGTGCCACCACGCCTG ATCTCTGCTCACTGCAACCTCCAACTGCAAGCGGCTGGGATTACAGTCATGTGCCACCACGCCTG T C CELF1 Ensembl:ENSG00000149187 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1020499130 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17560594 RMVar_hsa_circ_119120,RMVar_hsa_circ_37929,RMVar_hsa_circ_149551,RMVar_hsa_circ_288701,RMVar_hsa_circ_375912,RMVar_hsa_circ_332850,RMVar_hsa_circ_19919,RMVar_hsa_circ_35187,RMVar_hsa_circ_5549,RMVar_hsa_circ_19207,RMVar_hsa_circ_149553,RMVar_hsa_circ_149554,RMVar_hsa_circ_75150,RMVar_hsa_circ_149555,RMVar_hsa_circ_11194,RMVar_hsa_circ_295519,RMVar_hsa_circ_361828,RMVar_hsa_circ_348304,RMVar_hsa_circ_149556,RMVar_hsa_circ_283690,RMVar_hsa_circ_318259,RMVar_hsa_circ_341549,RMVar_hsa_circ_36084,RMVar_hsa_circ_149559,RMVar_hsa_circ_149560,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 6120 RMVar_ID_6120 Human_SNP_ID_465072943 A-to-I Human chr11 - 47482037 47482037 47482037 CATCACACCCAGCTAATTTTTGTATTTCTAGTAGGGATGGGCTTTCACTGTGTTGGCCAGGCTGG CATCACACCCAGCTAATTTTTGTATTTCTAGTGGGGATGGGCTTTCACTGTGTTGGCCAGGCTGG T C CELF1 Ensembl:ENSG00000149187 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1167950464 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6077411 RMVar_hsa_circ_119120,RMVar_hsa_circ_37929,RMVar_hsa_circ_149551,RMVar_hsa_circ_288701,RMVar_hsa_circ_375912,RMVar_hsa_circ_332850,RMVar_hsa_circ_19919,RMVar_hsa_circ_35187,RMVar_hsa_circ_5549,RMVar_hsa_circ_19207,RMVar_hsa_circ_149553,RMVar_hsa_circ_149554,RMVar_hsa_circ_75150,RMVar_hsa_circ_149555,RMVar_hsa_circ_11194,RMVar_hsa_circ_295519,RMVar_hsa_circ_361828,RMVar_hsa_circ_348304,RMVar_hsa_circ_149556,RMVar_hsa_circ_283690,RMVar_hsa_circ_318259,RMVar_hsa_circ_341549,RMVar_hsa_circ_36084,RMVar_hsa_circ_149559,RMVar_hsa_circ_149560,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 6121 RMVar_ID_6121 Human_SNP_ID_465072949 A-to-I Human chr11 - 47482102 47482102 47482102 CCACCTCGGGTTCAAGTGATTCTCCTGCCTCAACTTCCCAAGTAGCTGGGACTACAGACACACAC CCACCTCGGGTTCAAGTGATTCTCCTGCCTCAGCTTCCCAAGTAGCTGGGACTACAGACACACAC T C CELF1 Ensembl:ENSG00000149187 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1374626285 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23304982 RMVar_hsa_circ_119120,RMVar_hsa_circ_37929,RMVar_hsa_circ_149551,RMVar_hsa_circ_288701,RMVar_hsa_circ_375912,RMVar_hsa_circ_332850,RMVar_hsa_circ_19919,RMVar_hsa_circ_35187,RMVar_hsa_circ_5549,RMVar_hsa_circ_19207,RMVar_hsa_circ_149553,RMVar_hsa_circ_149554,RMVar_hsa_circ_75150,RMVar_hsa_circ_149555,RMVar_hsa_circ_11194,RMVar_hsa_circ_295519,RMVar_hsa_circ_361828,RMVar_hsa_circ_348304,RMVar_hsa_circ_149556,RMVar_hsa_circ_283690,RMVar_hsa_circ_318259,RMVar_hsa_circ_341549,RMVar_hsa_circ_36084,RMVar_hsa_circ_149559,RMVar_hsa_circ_149560,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 6122 RMVar_ID_6122 Human_SNP_ID_465072952 A-to-I Human chr11 - 47482120 47482120 47482120 CTTGGCTTACTGCAACCTCCACCTCGGGTTCAAGTGATTCTCCTGCCTCAACTTCCCAAGTAGCT CTTGGCTTACTGCAACCTCCACCTCGGGTTCAGGTGATTCTCCTGCCTCAACTTCCCAAGTAGCT T C CELF1 Ensembl:ENSG00000149187 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,frontal_cortex - 29129909,30559470 RNA-Seq:(High) rs574179343 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119120,RMVar_hsa_circ_37929,RMVar_hsa_circ_149551,RMVar_hsa_circ_288701,RMVar_hsa_circ_375912,RMVar_hsa_circ_332850,RMVar_hsa_circ_19919,RMVar_hsa_circ_35187,RMVar_hsa_circ_5549,RMVar_hsa_circ_19207,RMVar_hsa_circ_149553,RMVar_hsa_circ_149554,RMVar_hsa_circ_75150,RMVar_hsa_circ_149555,RMVar_hsa_circ_11194,RMVar_hsa_circ_295519,RMVar_hsa_circ_361828,RMVar_hsa_circ_348304,RMVar_hsa_circ_149556,RMVar_hsa_circ_283690,RMVar_hsa_circ_318259,RMVar_hsa_circ_341549,RMVar_hsa_circ_36084,RMVar_hsa_circ_149559,RMVar_hsa_circ_149560,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 6123 RMVar_ID_6123 Human_SNP_ID_465075656 A-to-I Human chr11 - 47492179 47492179 47492179 GCCCAGGAGTTTCAGACCAGCCCTTGCAACATAGTGAGACCCTCTCTCTACAAAAAAATGTTAAA GCCCAGGAGTTTCAGACCAGCCCTTGCAACATTGTGAGACCCTCTCTCTACAAAAAAATGTTAAA T A CELF1 Ensembl:ENSG00000149187 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1009054896 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_375912,RMVar_hsa_circ_332850,RMVar_hsa_circ_5549,RMVar_hsa_circ_149554,RMVar_hsa_circ_75150,RMVar_hsa_circ_348304,RMVar_hsa_circ_72610,RMVar_hsa_circ_342676,RMVar_hsa_circ_149564,RMVar_hsa_circ_290863,RMVar_hsa_circ_149567,RMVar_hsa_circ_116927,RMVar_hsa_circ_52645,RMVar_hsa_circ_149574,RMVar_hsa_circ_275263,RMVar_hsa_circ_149576 6124 RMVar_ID_6124 Human_SNP_ID_465075657 A-to-I Human chr11 - 47492179 47492179 47492179 GCCCAGGAGTTTCAGACCAGCCCTTGCAACATAGTGAGACCCTCTCTCTACAAAAAAATGTTAAA GCCCAGGAGTTTCAGACCAGCCCTTGCAACATGGTGAGACCCTCTCTCTACAAAAAAATGTTAAA T C CELF1 Ensembl:ENSG00000149187 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1009054896 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_375912,RMVar_hsa_circ_332850,RMVar_hsa_circ_5549,RMVar_hsa_circ_149554,RMVar_hsa_circ_75150,RMVar_hsa_circ_348304,RMVar_hsa_circ_72610,RMVar_hsa_circ_342676,RMVar_hsa_circ_149564,RMVar_hsa_circ_290863,RMVar_hsa_circ_149567,RMVar_hsa_circ_116927,RMVar_hsa_circ_52645,RMVar_hsa_circ_149574,RMVar_hsa_circ_275263,RMVar_hsa_circ_149576 6125 RMVar_ID_6125 Human_SNP_ID_465075681 A-to-I Human chr11 - 47492267 47492267 47492267 AAACACTCAAAAGAAAATAGGCCAGGCGCAGTAGTTCCATGCCTATAATCCCAGCACTTTGGGAG AAACACTCAAAAGAAAATAGGCCAGGCGCAGTGGTTCCATGCCTATAATCCCAGCACTTTGGGAG T C CELF1 Ensembl:ENSG00000149187 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1051382051 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_375912,RMVar_hsa_circ_332850,RMVar_hsa_circ_5549,RMVar_hsa_circ_149554,RMVar_hsa_circ_75150,RMVar_hsa_circ_348304,RMVar_hsa_circ_72610,RMVar_hsa_circ_342676,RMVar_hsa_circ_149564,RMVar_hsa_circ_290863,RMVar_hsa_circ_149567,RMVar_hsa_circ_116927,RMVar_hsa_circ_52645,RMVar_hsa_circ_149574,RMVar_hsa_circ_275263,RMVar_hsa_circ_149576 6126 RMVar_ID_6126 Human_SNP_ID_465075746 A-to-I Human chr11 - 47492547 47492547 47492547 CTTTGTATTTTTTGGTAGAGACGGAGTTTACCATGTTGGCCAGGGTGGTCTCGAACTCCTGACCT CTTTGTATTTTTTGGTAGAGACGGAGTTTACCGTGTTGGCCAGGGTGGTCTCGAACTCCTGACCT T C CELF1 Ensembl:ENSG00000149187 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1464416741 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24888055 RMVar_hsa_circ_375912,RMVar_hsa_circ_332850,RMVar_hsa_circ_5549,RMVar_hsa_circ_149554,RMVar_hsa_circ_75150,RMVar_hsa_circ_348304,RMVar_hsa_circ_72610,RMVar_hsa_circ_342676,RMVar_hsa_circ_149564,RMVar_hsa_circ_290863,RMVar_hsa_circ_149567,RMVar_hsa_circ_116927,RMVar_hsa_circ_52645,RMVar_hsa_circ_149574,RMVar_hsa_circ_275263,RMVar_hsa_circ_149576 6127 RMVar_ID_6127 Human_SNP_ID_465075750 A-to-I Human chr11 - 47492563 47492563 47492563 CACACCCAGCTAATTGCTTTGTATTTTTTGGTAGAGACGGAGTTTACCATGTTGGCCAGGGTGGT CACACCCAGCTAATTGCTTTGTATTTTTTGGTGGAGACGGAGTTTACCATGTTGGCCAGGGTGGT T C CELF1 Ensembl:ENSG00000149187 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1168724775 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_375912,RMVar_hsa_circ_332850,RMVar_hsa_circ_5549,RMVar_hsa_circ_149554,RMVar_hsa_circ_75150,RMVar_hsa_circ_348304,RMVar_hsa_circ_72610,RMVar_hsa_circ_342676,RMVar_hsa_circ_149564,RMVar_hsa_circ_290863,RMVar_hsa_circ_149567,RMVar_hsa_circ_116927,RMVar_hsa_circ_52645,RMVar_hsa_circ_149574,RMVar_hsa_circ_275263,RMVar_hsa_circ_149576 6128 RMVar_ID_6128 Human_SNP_ID_465078552 A-to-I Human chr11 - 47503978 47503978 47503978 GTAGAGATAGGTCTCTCTTTGTTGGTCAGACTAGTCTCAAACTCCTGGGCTTGAACAGTCTGCCC GTAGAGATAGGTCTCTCTTTGTTGGTCAGACTGGTCTCAAACTCCTGGGCTTGAACAGTCTGCCC T C CELF1 Ensembl:ENSG00000149187 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1321041910 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11634424 RMVar_hsa_circ_364920,RMVar_hsa_circ_149578,RMVar_hsa_circ_298170 6129 RMVar_ID_6129 Human_SNP_ID_465080810 A-to-I Human chr11 - 47512291 47512291 47512291 AAAATTAGCCAGGCTTGGTGGCCAGTGCCTGTAGTCCCAGCTACTCAGGAGGTTGAGGCAGGAGA AAAATTAGCCAGGCTTGGTGGCCAGTGCCTGTGGTCCCAGCTACTCAGGAGGTTGAGGCAGGAGA T C CELF1 Ensembl:ENSG00000149187 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1465090170 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_149579 6130 RMVar_ID_6130 Human_SNP_ID_465081816 A-to-I Human chr11 - 47516186 47516186 47516186 TCTCTTTTTATTTTTATTTTTTATTTTGAGACAGAGTCTTGCTCTGTCACCCAGGCTGGAGTGCA TCTCTTTTTATTTTTATTTTTTATTTTGAGACTGAGTCTTGCTCTGTCACCCAGGCTGGAGTGCA T A CELF1 Ensembl:ENSG00000149187 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1435353456 Functional Loss SNV dbSNP153 33..33 33 - - - 6131 RMVar_ID_6131 Human_SNP_ID_465082041 A-to-I Human chr11 - 47517062 47517062 47517062 TTGAATTTTTTTGTAGAGATAAGTCTCACTATATTGCCTGGGCTGGTCTGGAACTTGTGGGCTCA TTGAATTTTTTTGTAGAGATAAGTCTCACTATGTTGCCTGGGCTGGTCTGGAACTTGTGGGCTCA T C CELF1 Ensembl:ENSG00000149187 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1269790765 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11634843 6132 RMVar_ID_6132 Human_SNP_ID_465082621 A-to-I Human chr11 - 47519313 47519313 47519313 CCACGCCGGGCTAATTTGTTTGTATTTGTAGTAGAGATGGGGTTTCACCCCGTTGGCCAGGCTGG CCACGCCGGGCTAATTTGTTTGTATTTGTAGTGGAGATGGGGTTTCACCCCGTTGGCCAGGCTGG T C CELF1 Ensembl:ENSG00000149187 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1299389842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8352445,Human_RBP_ID_11634927 RMVar_hsa_circ_91451,RMVar_hsa_circ_149580 6133 RMVar_ID_6133 Human_SNP_ID_465083357 A-to-I Human chr11 - 47521973 47521973 47521973 CCGGGAGATGGAGGTTGTGATGAGCTGAGATCATGCCATTGCACTCCAGCCTGGGCAACAAGAGC CCGGGAGATGGAGGTTGTGATGAGCTGAGATCGTGCCATTGCACTCCAGCCTGGGCAACAAGAGC T C CELF1 Ensembl:ENSG00000149187 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1021983011 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9641697,Human_RBP_ID_23153984 6134 RMVar_ID_6134 Human_SNP_ID_465083396 A-to-I Human chr11 - 47522114 47522114 47522114 GAGGTCGGGAGTTCAAGACCAGCCTGACCAACATGGAGAAACCCCGTGTCTACTAAAAATACAAA GAGGTCGGGAGTTCAAGACCAGCCTGACCAACGTGGAGAAACCCCGTGTCTACTAAAAATACAAA T C CELF1 Ensembl:ENSG00000149187 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs962464006 Functional Loss SNV dbSNP153 33..33 33 - - - 6135 RMVar_ID_6135 Human_SNP_ID_465083491 A-to-I Human chr11 - 47522474 47522474 47522474 GCTCTGTCACCAAGGCTGGAGTGCAATGGCACAATCTCAGCTCACTGCAACCTCTGCCTCCCGGG GCTCTGTCACCAAGGCTGGAGTGCAATGGCACGATCTCAGCTCACTGCAACCTCTGCCTCCCGGG T C CELF1 Ensembl:ENSG00000149187 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1472162475 Functional Loss SNV dbSNP153 33..33 33 - - - 6136 RMVar_ID_6136 Human_SNP_ID_465085169 A-to-I Human chr11 - 47529216 47529205 47529217 GATTAGAAGTAGAAACTGGAGCCAGGAGCTATAGTGCCAGCTACCCGGGAGGCTGAGGTGGGATA GATTAGAAGTAGAAACTGGAGCCAGGAGCTA____________CCCGGGAGGCTGAGGTGGGATA GTAGCTGGCACTA G CELF1 Ensembl:ENSG00000149187 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1565891870 Functional Loss DEL dbSNP153 32..43 33 - - - Human_RBP_ID_9641735,Human_RBP_ID_11635361,Human_RBP_ID_24888292 6137 RMVar_ID_6137 Human_SNP_ID_465086251 A-to-I Human chr11 - 47533269 47533269 47533269 TTGGCCAGGCTAGTCTTGAATTCCTGACCTCAAGTGATCCCCCCGCCTCAGCTTCCCAAATTGCT TTGGCCAGGCTAGTCTTGAATTCCTGACCTCAGGTGATCCCCCCGCCTCAGCTTCCCAAATTGCT T C CELF1 Ensembl:ENSG00000149187 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037647380 Functional Loss SNV dbSNP153 33..33 33 - - - 6138 RMVar_ID_6138 Human_SNP_ID_465086285 A-to-I Human chr11 - 47533430 47533430 47533430 TTTAGTAGAGAGGGGGTTTCACCATGTTGCCCAGGCTGGTCGTGAACTCCTGAGCTCAGGCAATC TTTAGTAGAGAGGGGGTTTCACCATGTTGCCCGGGCTGGTCGTGAACTCCTGAGCTCAGGCAATC T C CELF1 Ensembl:ENSG00000149187 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1338070632 Functional Loss SNV dbSNP153 33..33 33 - - - 6139 RMVar_ID_6139 Human_SNP_ID_465086331 A-to-I Human chr11 - 47533571 47533571 47533571 TAGCCCAGGCTGGAGTGCGGTGGTGCGATCTCAGCTCACTGCCACTTCCGCCTTCCGGAGTTTAA TAGCCCAGGCTGGAGTGCGGTGGTGCGATCTCGGCTCACTGCCACTTCCGCCTTCCGGAGTTTAA T C CELF1 Ensembl:ENSG00000149187 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs534572969 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11768419 6140 RMVar_ID_6140 Human_SNP_ID_465086622 A-to-I Human chr11 - 47534132 47534132 47534132 CTCAGCTACTTCGGAGGCTGAGGCAGGAGAGTAGTTTGAACTAAGGAGGCGGAGGTTGCAGTGAG CTCAGCTACTTCGGAGGCTGAGGCAGGAGAGTGGTTTGAACTAAGGAGGCGGAGGTTGCAGTGAG T C CELF1 Ensembl:ENSG00000149187 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs999172722 Functional Loss SNV dbSNP153 33..33 33 - - - 6141 RMVar_ID_6141 Human_SNP_ID_465086689 A-to-I Human chr11 - 47534325 47534325 47534325 AAATCTTGATAGAAAAAATACTAAATATGGCCAGGCGCCGTGGCTCATGCCTGTAATCCCAGCAC AAATCTTGATAGAAAAAATACTAAATATGGCCTGGCGCCGTGGCTCATGCCTGTAATCCCAGCAC T A CELF1 Ensembl:ENSG00000149187 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1484997533 Functional Loss SNV dbSNP153 33..33 33 - - - 6142 RMVar_ID_6142 Human_SNP_ID_465089185 A-to-I Human chr11 - 47542361 47542359 47542361 GGTGCAGATACGGCTTTATTTATTTGAGACAGAGTTTCACTCTTGTTGCCCAGGGTGGAGTGCAG GGTGCAGATACGGCTTTATTTATTTGAGACAG__TTTCACTCTTGTTGCCCAGGGTGGAGTGCAG ACT A CELF1 Ensembl:ENSG00000149187 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs767069308 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_11635858 6143 RMVar_ID_6143 Human_SNP_ID_465089469 A-to-I Human chr11 - 47543397 47543397 47543397 GGGGCTTTTTTGGGCTGTTGTTTTCCGAGACAAGGTCTCATTGTGTCACTCAGGCTGGAGTGCAG GGGGCTTTTTTGGGCTGTTGTTTTCCGAGACAGGGTCTCATTGTGTCACTCAGGCTGGAGTGCAG T C CELF1 Ensembl:ENSG00000149187 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1473213186 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11635891,Human_RBP_ID_22471611 6144 RMVar_ID_6144 Human_SNP_ID_465089950 A-to-I Human chr11 - 47545384 47545384 47545384 CTCTGTCGCCCAGGCTAGCGTACAGTGGTTCAATCTCGGCTCACTGCAACCTCTGCTGGGAGGGG CTCTGTCGCCCAGGCTAGCGTACAGTGGTTCAGTCTCGGCTCACTGCAACCTCTGCTGGGAGGGG T C CELF1 Ensembl:ENSG00000149187 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1178323231 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11635976,Human_RBP_ID_23507686 6145 RMVar_ID_6145 Human_SNP_ID_465089955 A-to-I Human chr11 - 47545400 47545400 47545400 TTGAGACAGAGTCCCGCTCTGTCGCCCAGGCTAGCGTACAGTGGTTCAATCTCGGCTCACTGCAA TTGAGACAGAGTCCCGCTCTGTCGCCCAGGCTGGCGTACAGTGGTTCAATCTCGGCTCACTGCAA T C CELF1 Ensembl:ENSG00000149187 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1409972915 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227716,Human_RBP_ID_751314,Human_RBP_ID_11635979 6146 RMVar_ID_6146 Human_SNP_ID_465090054 A-to-I Human chr11 - 47545773 47545773 47545773 TAATCCCAGCACTTTGGAAGACTGAGGCGGGCAGATTGCTTGAGCTCAGGAGCTTGAGACCAGCC TAATCCCAGCACTTTGGAAGACTGAGGCGGGCGGATTGCTTGAGCTCAGGAGCTTGAGACCAGCC T C CELF1 Ensembl:ENSG00000149187 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1002806270 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_193704 6147 RMVar_ID_6147 Human_SNP_ID_465090513 A-to-I Human chr11 - 47546903 47546903 47546903 GCCATGACCCCCAGCTAATTTTTTGTATTTTTAGTAGAGACGGAGGTTTCTCCAGGTTGGTCAAG GCCATGACCCCCAGCTAATTTTTTGTATTTTTCGTAGAGACGGAGGTTTCTCCAGGTTGGTCAAG T G CELF1 Ensembl:ENSG00000149187 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs546315431 Functional Loss SNV dbSNP153 33..33 33 - - - 6148 RMVar_ID_6148 Human_SNP_ID_465090967 A-to-I Human chr11 - 47548187 47548183 47548187 TCAAGCGATTCTCCTACCTCAGCCTCCCGAGTAGCTGGGATTACAGGTTCCTGCCACTGTGCCTG TCAAGCGATTCTCCTACCTCAGCCTCCCGAGT____GGGATTACAGGTTCCTGCCACTGTGCCTG CAGCT C CELF1 Ensembl:ENSG00000149187 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1361404874 Functional Loss DEL dbSNP153 33..36 33 - - - 6149 RMVar_ID_6149 Human_SNP_ID_465090968 A-to-I Human chr11 - 47548187 47548187 47548187 TCAAGCGATTCTCCTACCTCAGCCTCCCGAGTAGCTGGGATTACAGGTTCCTGCCACTGTGCCTG TCAAGCGATTCTCCTACCTCAGCCTCCCGAGTGGCTGGGATTACAGGTTCCTGCCACTGTGCCTG T C CELF1 Ensembl:ENSG00000149187 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs569698797 Functional Loss SNV dbSNP153 33..33 33 - - - 6150 RMVar_ID_6150 Human_SNP_ID_465090975 A-to-I Human chr11 - 47548216 47548216 47548216 TGGCTCACTGCAATCTCTGTCGCCCTGGTTCAAGCGATTCTCCTACCTCAGCCTCCCGAGTAGCT TGGCTCACTGCAATCTCTGTCGCCCTGGTTCAGGCGATTCTCCTACCTCAGCCTCCCGAGTAGCT T C CELF1 Ensembl:ENSG00000149187 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs565647780 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11636076 6151 RMVar_ID_6151 Human_SNP_ID_465092990 A-to-I Human chr11 - 47554903 47554903 47554903 TCCCAGCACTTTGAGAGGCAGAGGCGGGCAGAACACTTGCAGTCAGGAGTTTGAGACCAGCCTGA TCCCAGCACTTTGAGAGGCAGAGGCGGGCAGATCACTTGCAGTCAGGAGTTTGAGACCAGCCTGA T A CELF1 Ensembl:ENSG00000149187 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1036254438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_397191 6152 RMVar_ID_6152 Human_SNP_ID_465093793 A-to-I Human chr11 - 47557993 47557992 47557993 AAATTAGTTGGGCATGCTGGCAGGTACAGGTAATTCCAGTTACTCGGGAGGATGAGGCAGGAGAA AAATTAGTTGGGCATGCTGGCAGGTACAGGTA_TTCCAGTTACTCGGGAGGATGAGGCAGGAGAA AT A CELF1 Ensembl:ENSG00000149187 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1420744164 Functional Loss DEL dbSNP153 33..33 33 - - - 6153 RMVar_ID_6153 Human_SNP_ID_465095450 A-to-I Human chr11 - 47563670 47563670 47563670 TATATTTTGTTTTTGAGACGGAGTCTCCTTCTATTGACTAGGCTGAAGTGTAGTGGCGCCATCTC TATATTTTGTTTTTGAGACGGAGTCTCCTTCTGTTGACTAGGCTGAAGTGTAGTGGCGCCATCTC T C CELF1 Ensembl:ENSG00000149187 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs549977473 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11636326 6154 RMVar_ID_6154 Human_SNP_ID_465096253 A-to-I Human chr11 + 47566372 47566372 47566372 GGGAGTGGTGGCGTGCGCCTGTACTCCCAGCTACTTGGGAGGCTAAGGCAGGAGAATCACTTTAG GGGAGTGGTGGCGTGCGCCTGTACTCCCAGCTGCTTGGGAGGCTAAGGCAGGAGAATCACTTTAG A G PTPMT1,NDUFS3 Ensembl:ENSG00000110536,Ensembl:ENSG00000213619 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1297144536 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107459,RMVar_hsa_circ_149582 6155 RMVar_ID_6155 Human_SNP_ID_465096825 A-to-I Human chr11 + 47568747 47568747 47568747 TTGTTTTGCTCTTGTCTCCCAGGCTGGAGTACAATGGTGCGATCTCTGCTCACTGCAACCTCTCC TTGTTTTGCTCTTGTCTCCCAGGCTGGAGTACGATGGTGCGATCTCTGCTCACTGCAACCTCTCC A G PTPMT1,NDUFS3 Ensembl:ENSG00000110536,Ensembl:ENSG00000213619 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs935390865 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107459,RMVar_hsa_circ_149582 6156 RMVar_ID_6156 Human_SNP_ID_465096840 A-to-I Human chr11 + 47568856 47568855 47568856 GGGATCACAGGCATCCACCACCACGCATGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCC GGGATCACAGGCATCCACCACCACGCATGGCT_ATTTTTGTATTTTTAGTAGAGACAGGGTTTCC TA T PTPMT1,NDUFS3 Ensembl:ENSG00000110536,Ensembl:ENSG00000213619 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs924443561 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_107459,RMVar_hsa_circ_149582 6157 RMVar_ID_6157 Human_SNP_ID_465096909 A-to-I Human chr11 + 47569176 47569176 47569176 GGGAGGCTGAGGCAGGCGGATGACCTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGATGA GGGAGGCTGAGGCAGGCGGATGACCTGAGGTCGGGAGTTCGAGACCAGCCTGGCCAACATGATGA A G PTPMT1,NDUFS3 Ensembl:ENSG00000110536,Ensembl:ENSG00000213619 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs912629339 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_108684 RMVar_hsa_circ_107459,RMVar_hsa_circ_149582 6158 RMVar_ID_6158 Human_SNP_ID_465097758 A-to-I Human chr11 + 47572574 47572574 47572574 TCACAGGCTATAGAACAAAAGTACAATTGGGCATCTTTCCTTATGTCCTGGGATCAGGGGTGCTT TCACAGGCTATAGAACAAAAGTACAATTGGGCCTCTTTCCTTATGTCCTGGGATCAGGGGTGCTT A C PTPMT1,NDUFS3 Ensembl:ENSG00000110536,Ensembl:ENSG00000213619 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs565904578 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11636386 Human_miRNA_ID_2626765,Human_miRNA_ID_2747592 RMVar_hsa_circ_107459,RMVar_hsa_circ_149582,RMVar_hsa_circ_96565,RMVar_hsa_circ_149584 6159 RMVar_ID_6159 Human_SNP_ID_465097768 A-to-I Human chr11 + 47572627 47572627 47572627 TCAGGGGTGCTTACATTTAACATTGATCAGGTAAAGAGGAGAGGCTGTGCCTAAGGTCTGAGAAA TCAGGGGTGCTTACATTTAACATTGATCAGGTGAAGAGGAGAGGCTGTGCCTAAGGTCTGAGAAA A G PTPMT1,NDUFS3 Ensembl:ENSG00000110536,Ensembl:ENSG00000213619 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1056618104 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_752487,Human_RBP_ID_11636394,Human_RBP_ID_23507717 RMVar_hsa_circ_107459,RMVar_hsa_circ_149582,RMVar_hsa_circ_96565,RMVar_hsa_circ_149584 6160 RMVar_ID_6160 Human_SNP_ID_465101049 A-to-I Human chr11 + 47582805 47582805 47582805 AGTGCTTGAGTCCAGGAGTTCGAGAACAGCCTAGGCAACATGGTGAAACCTCTTCTCTACAAAAA AGTGCTTGAGTCCAGGAGTTCGAGAACAGCCTCGGCAACATGGTGAAACCTCTTCTCTACAAAAA A C NDUFS3 Ensembl:ENSG00000213619 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1004864238 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107459,RMVar_hsa_circ_149582,RMVar_hsa_circ_96565,RMVar_hsa_circ_149584,RMVar_hsa_circ_84774,RMVar_hsa_circ_149590 6161 RMVar_ID_6161 Human_SNP_ID_465101088 A-to-I Human chr11 + 47582952 47582952 47582952 CTAGAAGGCGGAGGTTGCAGTGAGCCGAGATCACGCCACTGCTCTCCAGCCTGGGCAACAGAGTG CTAGAAGGCGGAGGTTGCAGTGAGCCGAGATCGCGCCACTGCTCTCCAGCCTGGGCAACAGAGTG A G NDUFS3 Ensembl:ENSG00000213619 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs55822708 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107459,RMVar_hsa_circ_149582,RMVar_hsa_circ_96565,RMVar_hsa_circ_149584,RMVar_hsa_circ_84774,RMVar_hsa_circ_149590 6162 RMVar_ID_6162 Human_SNP_ID_465109573 A-to-I Human chr11 - 47614023 47614023 47614023 TGTCTTGCAGTGGCTGATCTCGGCTCACTGCAACCTCCACCTCCTGGGTTCAAGCAATTCTCGTT TGTCTTGCAGTGGCTGATCTCGGCTCACTGCAGCCTCCACCTCCTGGGTTCAAGCAATTCTCGTT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1229926471 Functional Loss SNV dbSNP153 33..33 33 - - - 6163 RMVar_ID_6163 Human_SNP_ID_465110218 A-to-I Human chr11 - 47616506 47616504 47616506 CCTGGCCAATATATCTACTAAAAATACAAAAAAATTAGTCGGGCATGGTGGCACGCACCTGTAGT CCTGGCCAATATATCTACTAAAAATACAAAAA__TTAGTCGGGCATGGTGGCACGCACCTGTAGT ATT A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1043432954 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_24888602 6164 RMVar_ID_6164 Human_SNP_ID_465110219 A-to-I Human chr11 - 47616506 47616504 47616506 CCTGGCCAATATATCTACTAAAAATACAAAAAAATTAGTCGGGCATGGTGGCACGCACCTGTAGT CCTGGCCAATATATCTACTAAAAATACAAAAA_ATTAGTCGGGCATGGTGGCACGCACCTGTAGT ATT AT - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1043432954 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_24888602 6165 RMVar_ID_6165 Human_SNP_ID_465113755 A-to-I Human chr11 - 47631370 47631370 47631370 AGTTTCACTCTTGTTGCCCAGGCTGGAGTGCAATGGCACAATCTTGGCTCACTGCAACCTCAGCC AGTTTCACTCTTGTTGCCCAGGCTGGAGTGCAGTGGCACAATCTTGGCTCACTGCAACCTCAGCC T C MTCH2 Ensembl:ENSG00000109919 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1023073416 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118157,RMVar_hsa_circ_149594,RMVar_hsa_circ_101708,RMVar_hsa_circ_149593,RMVar_hsa_circ_363423,RMVar_hsa_circ_336867,RMVar_hsa_circ_275826,RMVar_hsa_circ_21540,RMVar_hsa_circ_149596,RMVar_hsa_circ_149597,RMVar_hsa_circ_149595,RMVar_hsa_circ_295381,RMVar_hsa_circ_278524,RMVar_hsa_circ_149608,RMVar_hsa_circ_149604,RMVar_hsa_circ_304166,RMVar_hsa_circ_376194,RMVar_hsa_circ_77511,RMVar_hsa_circ_149606,RMVar_hsa_circ_149607,RMVar_hsa_circ_331910,RMVar_hsa_circ_127394,RMVar_hsa_circ_149610,RMVar_hsa_circ_75981,RMVar_hsa_circ_149611,RMVar_hsa_circ_327658,RMVar_hsa_circ_149613 6166 RMVar_ID_6166 Human_SNP_ID_465115157 A-to-I Human chr11 - 47635931 47635931 47635931 TAGAGATGGGGTTTCACCATGTTGGCCAGGCTAGACTTGAACTCCTGACCTCAGGTGATCTGCCC TAGAGATGGGGTTTCACCATGTTGGCCAGGCTTGACTTGAACTCCTGACCTCAGGTGATCTGCCC T A MTCH2 Ensembl:ENSG00000109919 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1398679370 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_149608,RMVar_hsa_circ_304166,RMVar_hsa_circ_331910,RMVar_hsa_circ_149610,RMVar_hsa_circ_92371,RMVar_hsa_circ_122903,RMVar_hsa_circ_149615,RMVar_hsa_circ_149616,RMVar_hsa_circ_296967 6167 RMVar_ID_6167 Human_SNP_ID_465115163 A-to-I Human chr11 - 47635965 47635965 47635965 CGCCCCAATGCTCCGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGC CGCCCCAATGCTCCGCTAATTTTTGTATTTTTGGTAGAGATGGGGTTTCACCATGTTGGCCAGGC T C MTCH2 Ensembl:ENSG00000109919 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs763985066 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_149608,RMVar_hsa_circ_304166,RMVar_hsa_circ_331910,RMVar_hsa_circ_149610,RMVar_hsa_circ_92371,RMVar_hsa_circ_122903,RMVar_hsa_circ_149615,RMVar_hsa_circ_149616,RMVar_hsa_circ_296967 6168 RMVar_ID_6168 Human_SNP_ID_465115327 A-to-I Human chr11 - 47636569 47636569 47636569 TACCACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGAGGGGGTTTCGCCATGTCAGCCAGGC TACCACCACGCCCAGCTAATTTTTGTATTTTTGGTAGAGAGGGGGTTTCGCCATGTCAGCCAGGC T C MTCH2 Ensembl:ENSG00000109919 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1403231562 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_149608,RMVar_hsa_circ_304166,RMVar_hsa_circ_331910,RMVar_hsa_circ_149610,RMVar_hsa_circ_92371,RMVar_hsa_circ_122903,RMVar_hsa_circ_149615,RMVar_hsa_circ_149616,RMVar_hsa_circ_296967 6169 RMVar_ID_6169 Human_SNP_ID_465115350 A-to-I Human chr11 - 47636646 47636646 47636646 CTCACTGCAGCTTCCACCTACCGGGTTCAAGCAATTCTCCTGCCCCAGCTTCCCACGTAGCTGGG CTCACTGCAGCTTCCACCTACCGGGTTCAAGCGATTCTCCTGCCCCAGCTTCCCACGTAGCTGGG T C MTCH2 Ensembl:ENSG00000109919 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1436261036 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_149608,RMVar_hsa_circ_304166,RMVar_hsa_circ_331910,RMVar_hsa_circ_149610,RMVar_hsa_circ_92371,RMVar_hsa_circ_122903,RMVar_hsa_circ_149615,RMVar_hsa_circ_149616,RMVar_hsa_circ_296967 6170 RMVar_ID_6170 Human_SNP_ID_465116383 A-to-I Human chr11 - 47640283 47640283 47640283 CTCTTGTCACCCAGACTGGCATGCAATGGCACAATCTCGGCTCACTGCAACCTCCGCCTCCCAGG CTCTTGTCACCCAGACTGGCATGCAATGGCACGATCTCGGCTCACTGCAACCTCCGCCTCCCAGG T C MTCH2 Ensembl:ENSG00000109919 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs201631541 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92371,RMVar_hsa_circ_149616 6171 RMVar_ID_6171 Human_SNP_ID_465139791 A-to-I Human chr11 - 47733377 47733377 47733377 CAGAGATTGCTCCACTGTACTCTAGCCTGGGCAACAGAGCCAGAGTCCGAGTCCGTCTCTAAAAA CAGAGATTGCTCCACTGTACTCTAGCCTGGGCGACAGAGCCAGAGTCCGAGTCCGTCTCTAAAAA T C FNBP4 Ensembl:ENSG00000109920 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7107473 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_149624,RMVar_hsa_circ_72508,RMVar_hsa_circ_102697,RMVar_hsa_circ_149621,RMVar_hsa_circ_360503,RMVar_hsa_circ_83550,RMVar_hsa_circ_104369,RMVar_hsa_circ_73476,RMVar_hsa_circ_149625,RMVar_hsa_circ_44057,RMVar_hsa_circ_79080,RMVar_hsa_circ_149626,RMVar_hsa_circ_341159,RMVar_hsa_circ_363061,RMVar_hsa_circ_347752,RMVar_hsa_circ_280985,RMVar_hsa_circ_275399,RMVar_hsa_circ_334477,RMVar_hsa_circ_347418,RMVar_hsa_circ_267765,RMVar_hsa_circ_149628,RMVar_hsa_circ_149630,RMVar_hsa_circ_287,RMVar_hsa_circ_149629,RMVar_hsa_circ_149627,RMVar_hsa_circ_281683,RMVar_hsa_circ_318962,RMVar_hsa_circ_360840,RMVar_hsa_circ_304523,RMVar_hsa_circ_276943,RMVar_hsa_circ_149634,RMVar_hsa_circ_149635,RMVar_hsa_circ_149633,RMVar_hsa_circ_351317 6172 RMVar_ID_6172 Human_SNP_ID_465139804 A-to-I Human chr11 - 47733408 47733408 47733408 TCGCTTGAACCCAGGAGGTGAAGGTTGCGAGCAGAGATTGCTCCACTGTACTCTAGCCTGGGCAA TCGCTTGAACCCAGGAGGTGAAGGTTGCGAGCGGAGATTGCTCCACTGTACTCTAGCCTGGGCAA T C FNBP4 Ensembl:ENSG00000109920 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1284840226 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_149624,RMVar_hsa_circ_72508,RMVar_hsa_circ_102697,RMVar_hsa_circ_149621,RMVar_hsa_circ_360503,RMVar_hsa_circ_83550,RMVar_hsa_circ_104369,RMVar_hsa_circ_73476,RMVar_hsa_circ_149625,RMVar_hsa_circ_44057,RMVar_hsa_circ_79080,RMVar_hsa_circ_149626,RMVar_hsa_circ_341159,RMVar_hsa_circ_363061,RMVar_hsa_circ_347752,RMVar_hsa_circ_280985,RMVar_hsa_circ_275399,RMVar_hsa_circ_334477,RMVar_hsa_circ_347418,RMVar_hsa_circ_267765,RMVar_hsa_circ_149628,RMVar_hsa_circ_149630,RMVar_hsa_circ_287,RMVar_hsa_circ_149629,RMVar_hsa_circ_149627,RMVar_hsa_circ_281683,RMVar_hsa_circ_318962,RMVar_hsa_circ_360840,RMVar_hsa_circ_304523,RMVar_hsa_circ_276943,RMVar_hsa_circ_149634,RMVar_hsa_circ_149635,RMVar_hsa_circ_149633,RMVar_hsa_circ_351317 6173 RMVar_ID_6173 Human_SNP_ID_465140829 A-to-I Human chr11 - 47737011 47737011 47737011 TTTTAGTAGAGACGGTTCTACTGTGTTAGCCAAGATGGTCTCGATCTCCTGACCTCGTGATCTTT TTTTAGTAGAGACGGTTCTACTGTGTTAGCCAGGATGGTCTCGATCTCCTGACCTCGTGATCTTT T C FNBP4 Ensembl:ENSG00000109920 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1384338791 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18608569 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_149639 6174 RMVar_ID_6174 Human_SNP_ID_465141307 A-to-I Human chr11 - 47738773 47738773 47738773 GGAAGGCTGAGGCAGGAGAATTGCTTGAACCCAGGAGGTTGAGATTGCAATGAGCCGAGATAGCT GGAAGGCTGAGGCAGGAGAATTGCTTGAACCCGGGAGGTTGAGATTGCAATGAGCCGAGATAGCT T C FNBP4 Ensembl:ENSG00000109920 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs944824087 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23305000 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_149639 6175 RMVar_ID_6175 Human_SNP_ID_465141323 A-to-I Human chr11 - 47738837 47738837 47738837 AAAAAAAAAAAAAAAAAAAAAATTACCTGGGCATGGTGGCAAACACCTGAAGCCCCAGCTACTTG AAAAAAAAAAAAAAAAAAAAAATTACCTGGGCGTGGTGGCAAACACCTGAAGCCCCAGCTACTTG T C FNBP4 Ensembl:ENSG00000109920 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1166252735 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24889089 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_149639 6176 RMVar_ID_6176 Human_SNP_ID_465141464 A-to-I Human chr11 - 47739216 47739216 47739216 GACTTAATAAAAAGTTTTAGGCCGGATGCAATAGCTCAGCTTTAATCCCAGCATTCTGGGAGGCT GACTTAATAAAAAGTTTTAGGCCGGATGCAATGGCTCAGCTTTAATCCCAGCATTCTGGGAGGCT T C FNBP4 Ensembl:ENSG00000109920 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10769293 Functional Loss SNV dbSNP153 33..33 33 - - - 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_149639 6177 RMVar_ID_6177 Human_SNP_ID_465141691 A-to-I Human chr11 - 47740046 47740046 47740046 CCTATAATCCAAGCACTTTGGGAGACCGAGACAGACGGATCACCCGAGATTGAGAGTTCGAGACC CCTATAATCCAAGCACTTTGGGAGACCGAGACTGACGGATCACCCGAGATTGAGAGTTCGAGACC T A FNBP4 Ensembl:ENSG00000109920 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10838756 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11638226,Human_RBP_ID_23305459 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_149639 6178 RMVar_ID_6178 Human_SNP_ID_465141692 A-to-I Human chr11 - 47740046 47740046 47740046 CCTATAATCCAAGCACTTTGGGAGACCGAGACAGACGGATCACCCGAGATTGAGAGTTCGAGACC CCTATAATCCAAGCACTTTGGGAGACCGAGACGGACGGATCACCCGAGATTGAGAGTTCGAGACC T C FNBP4 Ensembl:ENSG00000109920 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10838756 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11638226,Human_RBP_ID_23305459 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_149639 6179 RMVar_ID_6179 Human_SNP_ID_465141704 A-to-I Human chr11 - 47740075 47740075 47740075 TAAGAGAGAGGATGTTGGCCTGGCTCACGCCTATAATCCAAGCACTTTGGGAGACCGAGACAGAC TAAGAGAGAGGATGTTGGCCTGGCTCACGCCTGTAATCCAAGCACTTTGGGAGACCGAGACAGAC T C FNBP4 Ensembl:ENSG00000109920 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs996709191 Functional Loss SNV dbSNP153 33..33 33 - - - 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_149639 6180 RMVar_ID_6180 Human_SNP_ID_465141739 A-to-I Human chr11 - 47740198 47740198 47740198 GTTGGCCAGGCTAATCTCGAACTCCCGACCTCAGGTGATCCGCCCGTCTCTGCCTCCCAAAGTGC GTTGGCCAGGCTAATCTCGAACTCCCGACCTCGGGTGATCCGCCCGTCTCTGCCTCCCAAAGTGC T C FNBP4 Ensembl:ENSG00000109920 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348569020 Functional Loss SNV dbSNP153 33..33 33 - - - 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_149639 6181 RMVar_ID_6181 Human_SNP_ID_465141740 A-to-I Human chr11 - 47740198 47740198 47740198 GTTGGCCAGGCTAATCTCGAACTCCCGACCTCAGGTGATCCGCCCGTCTCTGCCTCCCAAAGTGC GTTGGCCAGGCTAATCTCGAACTCCCGACCTCCGGTGATCCGCCCGTCTCTGCCTCCCAAAGTGC T G FNBP4 Ensembl:ENSG00000109920 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348569020 Functional Loss SNV dbSNP153 33..33 33 - - - 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_149639 6182 RMVar_ID_6182 Human_SNP_ID_465141767 A-to-I Human chr11 - 47740266 47740266 47740266 GGATTACAGGCGCACGCCACCTTGCGCAGCTAATTTTTGTATTTTTAGTACAGACAGGGTTTTAT GGATTACAGGCGCACGCCACCTTGCGCAGCTAGTTTTTGTATTTTTAGTACAGACAGGGTTTTAT T C FNBP4 Ensembl:ENSG00000109920 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1279993210 Functional Loss SNV dbSNP153 33..33 33 - - - 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_149639 6183 RMVar_ID_6183 Human_SNP_ID_465141914 A-to-I Human chr11 - 47740696 47740696 47740696 CCCAGCTACTTGGGAGACTGAGGCAGGAAATCACCTGAACCCAGGAGGCGGAAGTTGGAGTGAGC CCCAGCTACTTGGGAGACTGAGGCAGGAAATCGCCTGAACCCAGGAGGCGGAAGTTGGAGTGAGC T C FNBP4 Ensembl:ENSG00000109920 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1247706843 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8352584 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_149639 6184 RMVar_ID_6184 Human_SNP_ID_465142107 A-to-I Human chr11 - 47741369 47741369 47741369 AGGCCAGGAGTCAAGACCAGCCTGGACAATATAGCAAGACACTGTCTCTAAAATGTTTTTTAAAA AGGCCAGGAGTCAAGACCAGCCTGGACAATATGGCAAGACACTGTCTCTAAAATGTTTTTTAAAA T C FNBP4 Ensembl:ENSG00000109920 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1408891777 Functional Loss SNV dbSNP153 33..33 33 - - - 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_149639 6185 RMVar_ID_6185 Human_SNP_ID_465143757 A-to-I Human chr11 - 47747193 47747193 47747193 CTCAAAAACAGAAACAAAAATGAGCTGGGTGTAGTGGTGCATCCCTGTAATCCCAGCTACTTGGG CTCAAAAACAGAAACAAAAATGAGCTGGGTGTGGTGGTGCATCCCTGTAATCCCAGCTACTTGGG T C FNBP4 Ensembl:ENSG00000109920 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs149832964 Functional Loss SNV dbSNP153 33..33 33 - - - 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_149629,RMVar_hsa_circ_318962,RMVar_hsa_circ_360840,RMVar_hsa_circ_276943,RMVar_hsa_circ_149635,RMVar_hsa_circ_324092,RMVar_hsa_circ_56774,RMVar_hsa_circ_149638,RMVar_hsa_circ_71013,RMVar_hsa_circ_354843,RMVar_hsa_circ_267069,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_58118,RMVar_hsa_circ_294542 6186 RMVar_ID_6186 Human_SNP_ID_465143758 A-to-I Human chr11 - 47747193 47747193 47747193 CTCAAAAACAGAAACAAAAATGAGCTGGGTGTAGTGGTGCATCCCTGTAATCCCAGCTACTTGGG CTCAAAAACAGAAACAAAAATGAGCTGGGTGTCGTGGTGCATCCCTGTAATCCCAGCTACTTGGG T G FNBP4 Ensembl:ENSG00000109920 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs149832964 Functional Loss SNV dbSNP153 33..33 33 - - - 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_149629,RMVar_hsa_circ_318962,RMVar_hsa_circ_360840,RMVar_hsa_circ_276943,RMVar_hsa_circ_149635,RMVar_hsa_circ_324092,RMVar_hsa_circ_56774,RMVar_hsa_circ_149638,RMVar_hsa_circ_71013,RMVar_hsa_circ_354843,RMVar_hsa_circ_267069,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_58118,RMVar_hsa_circ_294542 6187 RMVar_ID_6187 Human_SNP_ID_465143802 A-to-I Human chr11 - 47747345 47747345 47747345 AAAAAATTAGCCAGGCTTGGTGGCTCTCGCCTATAATCCCAGCTGCTCAGGAGGCTGAGGCAGGG AAAAAATTAGCCAGGCTTGGTGGCTCTCGCCTGTAATCCCAGCTGCTCAGGAGGCTGAGGCAGGG T C FNBP4 Ensembl:ENSG00000109920 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1024197837 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22471613 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_149629,RMVar_hsa_circ_318962,RMVar_hsa_circ_360840,RMVar_hsa_circ_276943,RMVar_hsa_circ_149635,RMVar_hsa_circ_324092,RMVar_hsa_circ_56774,RMVar_hsa_circ_149638,RMVar_hsa_circ_71013,RMVar_hsa_circ_354843,RMVar_hsa_circ_267069,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_58118,RMVar_hsa_circ_294542 6188 RMVar_ID_6188 Human_SNP_ID_465143823 A-to-I Human chr11 - 47747411 47747411 47747411 CTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACGTGGTGAAACCCTGTGTCTACTAAAAGTACA CTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAGCGTGGTGAAACCCTGTGTCTACTAAAAGTACA T C FNBP4 Ensembl:ENSG00000109920 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs182351837 Functional Loss SNV dbSNP153 33..33 33 - - - 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_149629,RMVar_hsa_circ_318962,RMVar_hsa_circ_360840,RMVar_hsa_circ_276943,RMVar_hsa_circ_149635,RMVar_hsa_circ_324092,RMVar_hsa_circ_56774,RMVar_hsa_circ_149638,RMVar_hsa_circ_71013,RMVar_hsa_circ_354843,RMVar_hsa_circ_267069,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_58118,RMVar_hsa_circ_294542 6189 RMVar_ID_6189 Human_SNP_ID_465143944 A-to-I Human chr11 - 47747848 47747848 47747848 TGCCTCCCAGGTTCAAGCGATTCTTCTGCCTCAGCCTCCCGAATAGCTGGGATTACAGGCGCACG TGCCTCCCAGGTTCAAGCGATTCTTCTGCCTCCGCCTCCCGAATAGCTGGGATTACAGGCGCACG T G FNBP4 Ensembl:ENSG00000109920 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs893072409 Functional Loss SNV dbSNP153 33..33 33 - - - 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_149629,RMVar_hsa_circ_318962,RMVar_hsa_circ_360840,RMVar_hsa_circ_276943,RMVar_hsa_circ_149635,RMVar_hsa_circ_324092,RMVar_hsa_circ_56774,RMVar_hsa_circ_149638,RMVar_hsa_circ_71013,RMVar_hsa_circ_354843,RMVar_hsa_circ_267069,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_58118,RMVar_hsa_circ_294542 6190 RMVar_ID_6190 Human_SNP_ID_465147116 A-to-I Human chr11 - 47758694 47758694 47758694 CCACCACAGCCAGCTAATTTTTTGTTTTTAGTAGAGGTGGGATTTCACCATGTTGGCCAGGATAG CCACCACAGCCAGCTAATTTTTTGTTTTTAGTGGAGGTGGGATTTCACCATGTTGGCCAGGATAG T C FNBP4 Ensembl:ENSG00000109920 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1211347792 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104369,RMVar_hsa_circ_149625,RMVar_hsa_circ_360840,RMVar_hsa_circ_359423,RMVar_hsa_circ_90929,RMVar_hsa_circ_7244,RMVar_hsa_circ_149640,RMVar_hsa_circ_149647,RMVar_hsa_circ_149650,RMVar_hsa_circ_56304,RMVar_hsa_circ_268721 6191 RMVar_ID_6191 Human_SNP_ID_465147134 A-to-I Human chr11 - 47758772 47758772 47758772 TCACTGCAATGTCCACCTTCCGGGTTCAAGCAATTCTCATGCCTCAGCCTCCTGAGTAGCTGGGA TCACTGCAATGTCCACCTTCCGGGTTCAAGCAGTTCTCATGCCTCAGCCTCCTGAGTAGCTGGGA T C FNBP4 Ensembl:ENSG00000109920 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1459123572 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104369,RMVar_hsa_circ_149625,RMVar_hsa_circ_360840,RMVar_hsa_circ_359423,RMVar_hsa_circ_90929,RMVar_hsa_circ_7244,RMVar_hsa_circ_149640,RMVar_hsa_circ_149647,RMVar_hsa_circ_149650,RMVar_hsa_circ_56304,RMVar_hsa_circ_268721 6192 RMVar_ID_6192 Human_SNP_ID_465147149 A-to-I Human chr11 - 47758823 47758823 47758823 GACGGAGTCTCGCCCTGTCACCAGGCTGGAATACAGTGACGTGATCTCAGCTCACTGCAATGTCC GACGGAGTCTCGCCCTGTCACCAGGCTGGAATGCAGTGACGTGATCTCAGCTCACTGCAATGTCC T C FNBP4 Ensembl:ENSG00000109920 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1245407949 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17560312 RMVar_hsa_circ_104369,RMVar_hsa_circ_149625,RMVar_hsa_circ_360840,RMVar_hsa_circ_359423,RMVar_hsa_circ_90929,RMVar_hsa_circ_7244,RMVar_hsa_circ_149640,RMVar_hsa_circ_149647,RMVar_hsa_circ_149650,RMVar_hsa_circ_56304,RMVar_hsa_circ_268721 6193 RMVar_ID_6193 Human_SNP_ID_465147338 A-to-I Human chr11 - 47759396 47759396 47759396 CAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAAAATTAGCCAGGCGTGGT CAGCCTGGCCAACATGGTGAAACCCCATCTCTCCTAAAAATACAAAAAAATTAGCCAGGCGTGGT T G FNBP4 Ensembl:ENSG00000109920 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs955342196 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104369,RMVar_hsa_circ_149625,RMVar_hsa_circ_360840,RMVar_hsa_circ_359423,RMVar_hsa_circ_90929,RMVar_hsa_circ_7244,RMVar_hsa_circ_149640,RMVar_hsa_circ_149647,RMVar_hsa_circ_149650,RMVar_hsa_circ_56304,RMVar_hsa_circ_268721 6194 RMVar_ID_6194 Human_SNP_ID_465147866 A-to-I Human chr11 - 47761438 47761438 47761438 ACTGGCTCATGCCACCATCCCCAGCTAATTTTATATTTTTAGTAGAGACAGGGTTTCAGCATCTT ACTGGCTCATGCCACCATCCCCAGCTAATTTTTTATTTTTAGTAGAGACAGGGTTTCAGCATCTT T A FNBP4 Ensembl:ENSG00000109920 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs780251529 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104369,RMVar_hsa_circ_149625,RMVar_hsa_circ_360840,RMVar_hsa_circ_359423,RMVar_hsa_circ_90929,RMVar_hsa_circ_7244,RMVar_hsa_circ_149640,RMVar_hsa_circ_149647,RMVar_hsa_circ_149650,RMVar_hsa_circ_56304,RMVar_hsa_circ_268721 6195 RMVar_ID_6195 Human_SNP_ID_465147922 A-to-I Human chr11 - 47761667 47761667 47761667 GTGATCCTCCTTCCTTGGCCTCCCAAAATGCTAGGATTATAGATGTGAGCCACCGTGACCATCCT GTGATCCTCCTTCCTTGGCCTCCCAAAATGCTGGGATTATAGATGTGAGCCACCGTGACCATCCT T C FNBP4 Ensembl:ENSG00000109920 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1484628096 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2271237,Human_RBP_ID_11638641,Human_RBP_ID_17560605 RMVar_hsa_circ_104369,RMVar_hsa_circ_149625,RMVar_hsa_circ_360840,RMVar_hsa_circ_359423,RMVar_hsa_circ_90929,RMVar_hsa_circ_7244,RMVar_hsa_circ_149640,RMVar_hsa_circ_149647,RMVar_hsa_circ_149650,RMVar_hsa_circ_56304,RMVar_hsa_circ_268721 6196 RMVar_ID_6196 Human_SNP_ID_465148134 A-to-I Human chr11 - 47762399 47762399 47762399 AAATAGGCGGGGCACGGTGGTTCACGCGTGTAATTCCAGCACTTTGGGAGGCCAAGGCGGGCGGA AAATAGGCGGGGCACGGTGGTTCACGCGTGTAGTTCCAGCACTTTGGGAGGCCAAGGCGGGCGGA T C FNBP4 Ensembl:ENSG00000109920 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1399621198 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104369,RMVar_hsa_circ_149625,RMVar_hsa_circ_360840,RMVar_hsa_circ_359423,RMVar_hsa_circ_90929,RMVar_hsa_circ_7244,RMVar_hsa_circ_149640,RMVar_hsa_circ_149647,RMVar_hsa_circ_149650,RMVar_hsa_circ_56304,RMVar_hsa_circ_268721 6197 RMVar_ID_6197 Human_SNP_ID_465148215 A-to-I Human chr11 - 47762730 47762730 47762730 AATTTTTGTATTTTCAGTAGAGACGGTTCACCATGTTGGCCAGGCTGGTCTGGAACTCCTGACTT AATTTTTGTATTTTCAGTAGAGACGGTTCACCTTGTTGGCCAGGCTGGTCTGGAACTCCTGACTT T A FNBP4 Ensembl:ENSG00000109920 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs866561229 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104369,RMVar_hsa_circ_149625,RMVar_hsa_circ_360840,RMVar_hsa_circ_359423,RMVar_hsa_circ_90929,RMVar_hsa_circ_7244,RMVar_hsa_circ_149640,RMVar_hsa_circ_149647,RMVar_hsa_circ_149650,RMVar_hsa_circ_56304,RMVar_hsa_circ_268721 6198 RMVar_ID_6198 Human_SNP_ID_465148216 A-to-I Human chr11 - 47762730 47762730 47762730 AATTTTTGTATTTTCAGTAGAGACGGTTCACCATGTTGGCCAGGCTGGTCTGGAACTCCTGACTT AATTTTTGTATTTTCAGTAGAGACGGTTCACCGTGTTGGCCAGGCTGGTCTGGAACTCCTGACTT T C FNBP4 Ensembl:ENSG00000109920 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs866561229 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104369,RMVar_hsa_circ_149625,RMVar_hsa_circ_360840,RMVar_hsa_circ_359423,RMVar_hsa_circ_90929,RMVar_hsa_circ_7244,RMVar_hsa_circ_149640,RMVar_hsa_circ_149647,RMVar_hsa_circ_149650,RMVar_hsa_circ_56304,RMVar_hsa_circ_268721 6199 RMVar_ID_6199 Human_SNP_ID_465148568 A-to-I Human chr11 - 47763773 47763773 47763773 GCTCTGGGCCAGGCACAGTGGCTCACGCTTGTAATCCCAGCATTTTGGGAGGCCGAGGCAGGTGG GCTCTGGGCCAGGCACAGTGGCTCACGCTTGTGATCCCAGCATTTTGGGAGGCCGAGGCAGGTGG T C FNBP4 Ensembl:ENSG00000109920 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs922309522 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24889321 RMVar_hsa_circ_104369,RMVar_hsa_circ_149625,RMVar_hsa_circ_360840,RMVar_hsa_circ_359423,RMVar_hsa_circ_90929,RMVar_hsa_circ_7244,RMVar_hsa_circ_149640,RMVar_hsa_circ_149647,RMVar_hsa_circ_149650,RMVar_hsa_circ_56304,RMVar_hsa_circ_268721 6200 RMVar_ID_6200 Human_SNP_ID_465149258 A-to-I Human chr11 - 47765713 47765713 47765713 TGCCTCCTGGGTTCAAGCGATCCTTCTGCCTCAGCCTCCCGAGTAGTTGGGATTACAAGCGAGTG TGCCTCCTGGGTTCAAGCGATCCTTCTGCCTCTGCCTCCCGAGTAGTTGGGATTACAAGCGAGTG T A FNBP4 Ensembl:ENSG00000109920 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs899355555 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90929,RMVar_hsa_circ_149650 6201 RMVar_ID_6201 Human_SNP_ID_465153938 A-to-I Human chr11 - 47782070 47782070 47782070 ACCATGTTGGCCAGGCTGGTCTCGGAACTCCTAACCTCAAGTGATCCACCCACCTCGGCCTCCCA ACCATGTTGGCCAGGCTGGTCTCGGAACTCCTCACCTCAAGTGATCCACCCACCTCGGCCTCCCA T G NUP160 Ensembl:ENSG00000030066 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1436611745 Functional Loss SNV dbSNP153 33..33 33 - - - 6202 RMVar_ID_6202 Human_SNP_ID_465158511 A-to-I Human chr11 - 47798639 47798639 47798639 AAATTTTTTTGTAGAGATGGGGGTCTTGCCATATTGCCCAGGCTGGCCTTGAGCAATCCTGCTGC AAATTTTTTTGTAGAGATGGGGGTCTTGCCATCTTGCCCAGGCTGGCCTTGAGCAATCCTGCTGC T G NUP160 Ensembl:ENSG00000030066 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1407589284 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_373104,RMVar_hsa_circ_352463,RMVar_hsa_circ_42816,RMVar_hsa_circ_51616,RMVar_hsa_circ_31768,RMVar_hsa_circ_62759,RMVar_hsa_circ_149652,RMVar_hsa_circ_109870,RMVar_hsa_circ_50527,RMVar_hsa_circ_149657,RMVar_hsa_circ_149658,RMVar_hsa_circ_47121,RMVar_hsa_circ_27747,RMVar_hsa_circ_28477,RMVar_hsa_circ_104454,RMVar_hsa_circ_319393,RMVar_hsa_circ_340051,RMVar_hsa_circ_302165,RMVar_hsa_circ_92217,RMVar_hsa_circ_102271,RMVar_hsa_circ_45602,RMVar_hsa_circ_149662,RMVar_hsa_circ_149664,RMVar_hsa_circ_149665,RMVar_hsa_circ_149666,RMVar_hsa_circ_149663,RMVar_hsa_circ_115231,RMVar_hsa_circ_90337,RMVar_hsa_circ_345496,RMVar_hsa_circ_317760,RMVar_hsa_circ_149667,RMVar_hsa_circ_149668,RMVar_hsa_circ_117638,RMVar_hsa_circ_149671,RMVar_hsa_circ_94554,RMVar_hsa_circ_149673,RMVar_hsa_circ_57124,RMVar_hsa_circ_149672,RMVar_hsa_circ_285232,RMVar_hsa_circ_313095,RMVar_hsa_circ_294432,RMVar_hsa_circ_103615,RMVar_hsa_circ_119511,RMVar_hsa_circ_149675,RMVar_hsa_circ_149676,RMVar_hsa_circ_149677,RMVar_hsa_circ_106379,RMVar_hsa_circ_35496,RMVar_hsa_circ_149679,RMVar_hsa_circ_149680,RMVar_hsa_circ_149681,RMVar_hsa_circ_59503,RMVar_hsa_circ_11887 6203 RMVar_ID_6203 Human_SNP_ID_465158808 A-to-I Human chr11 - 47799812 47799812 47799812 AGTGGGTGCAGTGGCTCACGCCTGTAATCCCAACACTTTGAGAGGCTAAGGCAGGAGGATCACTG AGTGGGTGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGAGAGGCTAAGGCAGGAGGATCACTG T C NUP160 Ensembl:ENSG00000030066 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs998097345 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_373104,RMVar_hsa_circ_352463,RMVar_hsa_circ_42816,RMVar_hsa_circ_51616,RMVar_hsa_circ_31768,RMVar_hsa_circ_62759,RMVar_hsa_circ_149652,RMVar_hsa_circ_109870,RMVar_hsa_circ_50527,RMVar_hsa_circ_149657,RMVar_hsa_circ_149658,RMVar_hsa_circ_47121,RMVar_hsa_circ_27747,RMVar_hsa_circ_28477,RMVar_hsa_circ_104454,RMVar_hsa_circ_319393,RMVar_hsa_circ_340051,RMVar_hsa_circ_302165,RMVar_hsa_circ_92217,RMVar_hsa_circ_102271,RMVar_hsa_circ_45602,RMVar_hsa_circ_149662,RMVar_hsa_circ_149664,RMVar_hsa_circ_149665,RMVar_hsa_circ_149666,RMVar_hsa_circ_149663,RMVar_hsa_circ_115231,RMVar_hsa_circ_90337,RMVar_hsa_circ_345496,RMVar_hsa_circ_317760,RMVar_hsa_circ_149667,RMVar_hsa_circ_149668,RMVar_hsa_circ_117638,RMVar_hsa_circ_149671,RMVar_hsa_circ_94554,RMVar_hsa_circ_149673,RMVar_hsa_circ_57124,RMVar_hsa_circ_149672,RMVar_hsa_circ_285232,RMVar_hsa_circ_313095,RMVar_hsa_circ_294432,RMVar_hsa_circ_103615,RMVar_hsa_circ_119511,RMVar_hsa_circ_149675,RMVar_hsa_circ_149676,RMVar_hsa_circ_149677,RMVar_hsa_circ_106379,RMVar_hsa_circ_35496,RMVar_hsa_circ_149679,RMVar_hsa_circ_149680,RMVar_hsa_circ_149681,RMVar_hsa_circ_59503,RMVar_hsa_circ_11887 6204 RMVar_ID_6204 Human_SNP_ID_465163236 A-to-I Human chr11 - 47816518 47816518 47816518 CACCCGCCTCAGCCTCCCAAAGTGCTGGGATTATAGGCATGAGCCACCACACCCAGCTTGCATAG CACCCGCCTCAGCCTCCCAAAGTGCTGGGATTGTAGGCATGAGCCACCACACCCAGCTTGCATAG T C NUP160 Ensembl:ENSG00000030066 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1202734203 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4885,RMVar_hsa_circ_373104,RMVar_hsa_circ_31768,RMVar_hsa_circ_62759,RMVar_hsa_circ_149652,RMVar_hsa_circ_109870,RMVar_hsa_circ_149658,RMVar_hsa_circ_27747,RMVar_hsa_circ_28477,RMVar_hsa_circ_115231,RMVar_hsa_circ_90337,RMVar_hsa_circ_149667,RMVar_hsa_circ_149673,RMVar_hsa_circ_103615,RMVar_hsa_circ_149679,RMVar_hsa_circ_269747,RMVar_hsa_circ_59747,RMVar_hsa_circ_28324,RMVar_hsa_circ_87719,RMVar_hsa_circ_327508,RMVar_hsa_circ_34452,RMVar_hsa_circ_149685,RMVar_hsa_circ_149686,RMVar_hsa_circ_372538,RMVar_hsa_circ_320412,RMVar_hsa_circ_149687,RMVar_hsa_circ_149688,RMVar_hsa_circ_302860,RMVar_hsa_circ_38226,RMVar_hsa_circ_99327,RMVar_hsa_circ_149694,RMVar_hsa_circ_125713,RMVar_hsa_circ_303579,RMVar_hsa_circ_149697,RMVar_hsa_circ_149698,RMVar_hsa_circ_289312,RMVar_hsa_circ_302304,RMVar_hsa_circ_65185,RMVar_hsa_circ_149703,RMVar_hsa_circ_149700,RMVar_hsa_circ_288119,RMVar_hsa_circ_264887,RMVar_hsa_circ_312027,RMVar_hsa_circ_278189,RMVar_hsa_circ_149702,RMVar_hsa_circ_8092 6205 RMVar_ID_6205 Human_SNP_ID_465163248 A-to-I Human chr11 - 47816582 47816582 47816582 TTAGTAGAGACAAGGTTTTGCCATATTGGCCAAGCTTGTCTCGAACTCCTGGCCTCAAATGATCC TTAGTAGAGACAAGGTTTTGCCATATTGGCCACGCTTGTCTCGAACTCCTGGCCTCAAATGATCC T G NUP160 Ensembl:ENSG00000030066 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs555551620 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4885,RMVar_hsa_circ_373104,RMVar_hsa_circ_31768,RMVar_hsa_circ_62759,RMVar_hsa_circ_149652,RMVar_hsa_circ_109870,RMVar_hsa_circ_149658,RMVar_hsa_circ_27747,RMVar_hsa_circ_28477,RMVar_hsa_circ_115231,RMVar_hsa_circ_90337,RMVar_hsa_circ_149667,RMVar_hsa_circ_149673,RMVar_hsa_circ_103615,RMVar_hsa_circ_149679,RMVar_hsa_circ_269747,RMVar_hsa_circ_59747,RMVar_hsa_circ_28324,RMVar_hsa_circ_87719,RMVar_hsa_circ_327508,RMVar_hsa_circ_34452,RMVar_hsa_circ_149685,RMVar_hsa_circ_149686,RMVar_hsa_circ_372538,RMVar_hsa_circ_320412,RMVar_hsa_circ_149687,RMVar_hsa_circ_149688,RMVar_hsa_circ_302860,RMVar_hsa_circ_38226,RMVar_hsa_circ_99327,RMVar_hsa_circ_149694,RMVar_hsa_circ_125713,RMVar_hsa_circ_303579,RMVar_hsa_circ_149697,RMVar_hsa_circ_149698,RMVar_hsa_circ_289312,RMVar_hsa_circ_302304,RMVar_hsa_circ_65185,RMVar_hsa_circ_149703,RMVar_hsa_circ_149700,RMVar_hsa_circ_288119,RMVar_hsa_circ_264887,RMVar_hsa_circ_312027,RMVar_hsa_circ_278189,RMVar_hsa_circ_149702,RMVar_hsa_circ_8092 6206 RMVar_ID_6206 Human_SNP_ID_465165436 A-to-I Human chr11 - 47824523 47824523 47824523 TCACTGCAAGCTCCGCCTCCCGGGTTCACACCATTCTCCTACCTCAGCCTCTCGAATAGCTGGGA TCACTGCAAGCTCCGCCTCCCGGGTTCACACCGTTCTCCTACCTCAGCCTCTCGAATAGCTGGGA T C NUP160 Ensembl:ENSG00000030066 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs927106411 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24916943 RMVar_hsa_circ_31768,RMVar_hsa_circ_27747,RMVar_hsa_circ_115231,RMVar_hsa_circ_149673,RMVar_hsa_circ_103615,RMVar_hsa_circ_149679,RMVar_hsa_circ_28324,RMVar_hsa_circ_87719,RMVar_hsa_circ_149686,RMVar_hsa_circ_99327,RMVar_hsa_circ_149694,RMVar_hsa_circ_125713,RMVar_hsa_circ_149698,RMVar_hsa_circ_289312,RMVar_hsa_circ_149700,RMVar_hsa_circ_312027,RMVar_hsa_circ_331740,RMVar_hsa_circ_8092,RMVar_hsa_circ_350262,RMVar_hsa_circ_149705,RMVar_hsa_circ_80207,RMVar_hsa_circ_46979,RMVar_hsa_circ_37606,RMVar_hsa_circ_304667,RMVar_hsa_circ_346288,RMVar_hsa_circ_149707,RMVar_hsa_circ_336155 6207 RMVar_ID_6207 Human_SNP_ID_465166167 A-to-I Human chr11 - 47827107 47827107 47827107 CCACCTCGGCTTCCCAATGTGCTGGGATTACAAGTGTGAACCACAGCACCCAGCCTGAATTTTTC CCACCTCGGCTTCCCAATGTGCTGGGATTACAGGTGTGAACCACAGCACCCAGCCTGAATTTTTC T C NUP160 Ensembl:ENSG00000030066 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1389507844 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1238562,Human_Splice_Rec_1238563 RMVar_hsa_circ_31768,RMVar_hsa_circ_27747,RMVar_hsa_circ_115231,RMVar_hsa_circ_149673,RMVar_hsa_circ_103615,RMVar_hsa_circ_149679,RMVar_hsa_circ_28324,RMVar_hsa_circ_87719,RMVar_hsa_circ_149686,RMVar_hsa_circ_99327,RMVar_hsa_circ_149694,RMVar_hsa_circ_125713,RMVar_hsa_circ_149698,RMVar_hsa_circ_289312,RMVar_hsa_circ_149700,RMVar_hsa_circ_312027,RMVar_hsa_circ_331740,RMVar_hsa_circ_8092,RMVar_hsa_circ_350262,RMVar_hsa_circ_149705,RMVar_hsa_circ_80207,RMVar_hsa_circ_46979,RMVar_hsa_circ_37606,RMVar_hsa_circ_304667,RMVar_hsa_circ_346288,RMVar_hsa_circ_149707,RMVar_hsa_circ_336155,RMVar_hsa_circ_320032 6208 RMVar_ID_6208 Human_SNP_ID_465166169 A-to-I Human chr11 - 47827110 47827110 47827110 CACCCACCTCGGCTTCCCAATGTGCTGGGATTACAAGTGTGAACCACAGCACCCAGCCTGAATTT CACCCACCTCGGCTTCCCAATGTGCTGGGATTGCAAGTGTGAACCACAGCACCCAGCCTGAATTT T C NUP160 Ensembl:ENSG00000030066 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1319644150 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1238562,Human_Splice_Rec_1238563 RMVar_hsa_circ_31768,RMVar_hsa_circ_27747,RMVar_hsa_circ_115231,RMVar_hsa_circ_149673,RMVar_hsa_circ_103615,RMVar_hsa_circ_149679,RMVar_hsa_circ_28324,RMVar_hsa_circ_87719,RMVar_hsa_circ_149686,RMVar_hsa_circ_99327,RMVar_hsa_circ_149694,RMVar_hsa_circ_125713,RMVar_hsa_circ_149698,RMVar_hsa_circ_289312,RMVar_hsa_circ_149700,RMVar_hsa_circ_312027,RMVar_hsa_circ_331740,RMVar_hsa_circ_8092,RMVar_hsa_circ_350262,RMVar_hsa_circ_149705,RMVar_hsa_circ_80207,RMVar_hsa_circ_46979,RMVar_hsa_circ_37606,RMVar_hsa_circ_304667,RMVar_hsa_circ_346288,RMVar_hsa_circ_149707,RMVar_hsa_circ_336155,RMVar_hsa_circ_320032 6209 RMVar_ID_6209 Human_SNP_ID_465166407 A-to-I Human chr11 - 47828010 47828010 47828010 CAAAAATTAGCTGAGCATGGTGGCTCATTCCTATAGTACCAGCTATTTGAGGGGCTGAGATGGCA CAAAAATTAGCTGAGCATGGTGGCTCATTCCTGTAGTACCAGCTATTTGAGGGGCTGAGATGGCA T C NUP160 Ensembl:ENSG00000030066 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1168859667 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_31768,RMVar_hsa_circ_27747,RMVar_hsa_circ_115231,RMVar_hsa_circ_149673,RMVar_hsa_circ_103615,RMVar_hsa_circ_149679,RMVar_hsa_circ_28324,RMVar_hsa_circ_87719,RMVar_hsa_circ_149686,RMVar_hsa_circ_99327,RMVar_hsa_circ_149694,RMVar_hsa_circ_125713,RMVar_hsa_circ_149698,RMVar_hsa_circ_289312,RMVar_hsa_circ_149700,RMVar_hsa_circ_312027,RMVar_hsa_circ_331740,RMVar_hsa_circ_8092,RMVar_hsa_circ_350262,RMVar_hsa_circ_149705,RMVar_hsa_circ_80207,RMVar_hsa_circ_46979,RMVar_hsa_circ_37606,RMVar_hsa_circ_304667,RMVar_hsa_circ_346288,RMVar_hsa_circ_149707,RMVar_hsa_circ_336155,RMVar_hsa_circ_320032 6210 RMVar_ID_6210 Human_SNP_ID_465169245 A-to-I Human chr11 - 47839366 47839366 47839366 AACCCAAGGGCCAGGCGCTGTGGCTCACGTCTATAATCCCAGCACTGTGGGAGGCCAAGGCAGGT AACCCAAGGGCCAGGCGCTGTGGCTCACGTCTGTAATCCCAGCACTGTGGGAGGCCAAGGCAGGT T C NUP160 Ensembl:ENSG00000030066 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1032775576 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8352676 RMVar_hsa_circ_115231,RMVar_hsa_circ_149673,RMVar_hsa_circ_103615,RMVar_hsa_circ_149679,RMVar_hsa_circ_28324,RMVar_hsa_circ_125713,RMVar_hsa_circ_149698,RMVar_hsa_circ_312027,RMVar_hsa_circ_8092,RMVar_hsa_circ_350262,RMVar_hsa_circ_45497,RMVar_hsa_circ_149705,RMVar_hsa_circ_80207,RMVar_hsa_circ_46979,RMVar_hsa_circ_37606,RMVar_hsa_circ_346288,RMVar_hsa_circ_279109,RMVar_hsa_circ_43917,RMVar_hsa_circ_149709 6211 RMVar_ID_6211 Human_SNP_ID_465170822 A-to-I Human chr11 - 47846053 47846053 47846053 TGGCTTACTGCAGTCTCCGCCTCCTGGGTTCAAGTGACCCTCCCACCTCAGCCTCCCAAGTAGCT TGGCTTACTGCAGTCTCCGCCTCCTGGGTTCATGTGACCCTCCCACCTCAGCCTCCCAAGTAGCT T A NUP160 Ensembl:ENSG00000030066 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1382686259 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 6212 RMVar_ID_6212 Human_SNP_ID_465185341 A-to-I Human chr11 - 47905526 47905526 47905526 CTCCCAGCAAAGCCGTGGCCGCCCGGGCAGCAAGATCCACTGTCCGGCAGAGGAAAAATGCCAGC CTCCCAGCAAAGCCGTGGCCGCCCGGGCAGCAGGATCCACTGTCCGGCAGAGGAAAAATGCCAGC T C AC023232.1 Ensembl:ENSG00000254780 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878909508 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1864805,Human_miRNA_ID_1906460 6213 RMVar_ID_6213 Human_SNP_ID_465185342 A-to-I Human chr11 - 47905527 47905527 47905527 TCTCCCAGCAAAGCCGTGGCCGCCCGGGCAGCAAGATCCACTGTCCGGCAGAGGAAAAATGCCAG TCTCCCAGCAAAGCCGTGGCCGCCCGGGCAGCGAGATCCACTGTCCGGCAGAGGAAAAATGCCAG T C AC023232.1 Ensembl:ENSG00000254780 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879085346 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1864805,Human_miRNA_ID_1906460 6214 RMVar_ID_6214 Human_SNP_ID_465185345 A-to-I Human chr11 - 47905530 47905530 47905530 CACTCTCCCAGCAAAGCCGTGGCCGCCCGGGCAGCAAGATCCACTGTCCGGCAGAGGAAAAATGC CACTCTCCCAGCAAAGCCGTGGCCGCCCGGGCGGCAAGATCCACTGTCCGGCAGAGGAAAAATGC T C AC023232.1 Ensembl:ENSG00000254780 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878957081 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1864805,Human_miRNA_ID_1906460 6215 RMVar_ID_6215 Human_SNP_ID_465206968 A-to-I Human chr11 + 47994121 47994121 47994121 GAGCTCCGGCAATCCACCCGCTGCAGTCTCCCAAAGTGCTGGGATTACAGTTGTGAGCCACTGTG GAGCTCCGGCAATCCACCCGCTGCAGTCTCCCGAAGTGCTGGGATTACAGTTGTGAGCCACTGTG A G PTPRJ Ensembl:ENSG00000149177 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1303193888 Functional Loss SNV dbSNP153 33..33 33 - - - 6216 RMVar_ID_6216 Human_SNP_ID_465208622 A-to-I Human chr11 + 48001182 48001182 48001182 CACCTAGCTAGTTTTTGTGTTTTCGTAGAAACAAGGTTTCACCATGTTTGCCAGGCTGGTCTTGA CACCTAGCTAGTTTTTGTGTTTTCGTAGAAACGAGGTTTCACCATGTTTGCCAGGCTGGTCTTGA A G PTPRJ Ensembl:ENSG00000149177 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1193715601 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11640636 6217 RMVar_ID_6217 Human_SNP_ID_465213743 A-to-I Human chr11 + 48023671 48023671 48023671 GGGTGTGGTGGTGCGCGCCTGTAGTCCCAGCTACTTGTGAGGCTGAGGTAGGAGAATCACTTGAA GGGTGTGGTGGTGCGCGCCTGTAGTCCCAGCTGCTTGTGAGGCTGAGGTAGGAGAATCACTTGAA A G PTPRJ Ensembl:ENSG00000149177 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs897025678 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22891151 6218 RMVar_ID_6218 Human_SNP_ID_465213760 A-to-I Human chr11 + 48023757 48023757 48023757 TGAGCCGAGATCACACCATTGTACTCCAGCCTAGGCGACAGAGTGAGACTCGGACTCAAAAATAA TGAGCCGAGATCACACCATTGTACTCCAGCCTGGGCGACAGAGTGAGACTCGGACTCAAAAATAA A G PTPRJ Ensembl:ENSG00000149177 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1292297291 Functional Loss SNV dbSNP153 33..33 33 - - - 6219 RMVar_ID_6219 Human_SNP_ID_465213923 A-to-I Human chr11 + 48024337 48024337 48024337 CTCCTGTCTCAGCCTCCCGAGTAGCTGGGACTACAGACGCATGCCACCACAGCCGGCTAATTTTT CTCCTGTCTCAGCCTCCCGAGTAGCTGGGACTGCAGACGCATGCCACCACAGCCGGCTAATTTTT A G PTPRJ Ensembl:ENSG00000149177 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355389528 Functional Loss SNV dbSNP153 33..33 33 - - - 6220 RMVar_ID_6220 Human_SNP_ID_465224745 A-to-I Human chr11 + 48069334 48069334 48069334 GTTGGCCAGACTGGTCTTGAACTCCTGACCTCAAGAATCCACCTGCCTTGGCCTCCCAAAGTGCT GTTGGCCAGACTGGTCTTGAACTCCTGACCTCCAGAATCCACCTGCCTTGGCCTCCCAAAGTGCT A C PTPRJ Ensembl:ENSG00000149177 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs942701149 Functional Loss SNV dbSNP153 33..33 33 - - - 6221 RMVar_ID_6221 Human_SNP_ID_465227999 A-to-I Human chr11 + 48083264 48083264 48083264 CCTGACCAACATGGTGAAACCATATCTCTACTAAAAATAAAAAATTAGCTGAGCGTGGTGGTGTG CCTGACCAACATGGTGAAACCATATCTCTACTGAAAATAAAAAATTAGCTGAGCGTGGTGGTGTG A G PTPRJ Ensembl:ENSG00000149177 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs574860409 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2271616 6222 RMVar_ID_6222 Human_SNP_ID_465231264 A-to-I Human chr11 + 48097777 48097777 48097777 CCCAGGCTAGTCTCAAACTCCTGAGCTCAGGCAATCCCCAGCCTCAGCCCCCCAAAGTGCTAGGA CCCAGGCTAGTCTCAAACTCCTGAGCTCAGGCTATCCCCAGCCTCAGCCCCCCAAAGTGCTAGGA A T PTPRJ Ensembl:ENSG00000149177 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1296489904 Functional Loss SNV dbSNP153 33..33 33 - - - 6223 RMVar_ID_6223 Human_SNP_ID_123749663 A-to-I Human chr3 + 15020842 15020842 15020842 TGAGGAAAAATTTGACCTACAGCTGCCGGAGCAACCAAGACTGCATCATCAATAAACATCACCGG TGAGGAAAAATTTGACCTACAGCTGCCGGAGCGACCAAGACTGCATCATCAATAAACATCACCGG A G NR2C2 Ensembl:ENSG00000177463 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1320790412 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1952319,Human_RBP_ID_3964778,Human_RBP_ID_14672044,Human_RBP_ID_17288693,Human_RBP_ID_18012722,Human_RBP_ID_27499177 Human_Splice_Rec_398036,Human_Splice_Rec_398037,Human_Splice_Rec_398072,Human_Splice_Rec_398073,Human_Splice_Rec_398100,Human_Splice_Rec_398101,Human_Splice_Rec_398124,Human_Splice_Rec_398125,Human_Splice_Rec_398152,Human_Splice_Rec_398158,Human_Splice_Rec_398159,Human_Splice_Rec_398184,Human_Splice_Rec_398185 RMVar_hsa_circ_216097,RMVar_hsa_circ_24163,RMVar_hsa_circ_331601,RMVar_hsa_circ_371945,RMVar_hsa_circ_378209,RMVar_hsa_circ_343621,RMVar_hsa_circ_123808,RMVar_hsa_circ_24124,RMVar_hsa_circ_216098,RMVar_hsa_circ_216105,RMVar_hsa_circ_21219,RMVar_hsa_circ_295747,RMVar_hsa_circ_329903,RMVar_hsa_circ_216095,RMVar_hsa_circ_216096,RMVar_hsa_circ_373433,RMVar_hsa_circ_331371,RMVar_hsa_circ_321355,RMVar_hsa_circ_311004,RMVar_hsa_circ_282084,RMVar_hsa_circ_216107,RMVar_hsa_circ_216108,RMVar_hsa_circ_216106,RMVar_hsa_circ_54468,RMVar_hsa_circ_216103,RMVar_hsa_circ_216104,RMVar_hsa_circ_278508,RMVar_hsa_circ_280593,RMVar_hsa_circ_307390,RMVar_hsa_circ_122688,RMVar_hsa_circ_216112,RMVar_hsa_circ_216114,RMVar_hsa_circ_216115,RMVar_hsa_circ_216113,RMVar_hsa_circ_6509 6224 RMVar_ID_6224 Human_SNP_ID_123752442 A-to-I Human chr3 + 15031467 15031467 15031467 CCTCAAACTCCTGGTCTTGAACTCCTGGGCTCAGGTGATCCTCCTGCCTCAGCCTCCCAAGTAGC CCTCAAACTCCTGGTCTTGAACTCCTGGGCTCGGGTGATCCTCCTGCCTCAGCCTCCCAAGTAGC A G NR2C2 Ensembl:ENSG00000177463 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1358645881 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_216097,RMVar_hsa_circ_371945,RMVar_hsa_circ_343621,RMVar_hsa_circ_123808,RMVar_hsa_circ_216105,RMVar_hsa_circ_295747,RMVar_hsa_circ_216095,RMVar_hsa_circ_216096,RMVar_hsa_circ_373433,RMVar_hsa_circ_311004,RMVar_hsa_circ_54468,RMVar_hsa_circ_216103,RMVar_hsa_circ_216104,RMVar_hsa_circ_307390,RMVar_hsa_circ_36715,RMVar_hsa_circ_216112,RMVar_hsa_circ_8100,RMVar_hsa_circ_293590,RMVar_hsa_circ_309201,RMVar_hsa_circ_216118,RMVar_hsa_circ_288953,RMVar_hsa_circ_36064,RMVar_hsa_circ_216120 6225 RMVar_ID_6225 Human_SNP_ID_123752547 A-to-I Human chr3 + 15031918 15031917 15031919 ACCTGGCTAATTTTTGTATTTTTAATAGAGACAGGGTTTCATTATGTTGCCCAGGCTGGTCTCGA ACCTGGCTAATTTTTGTATTTTTAATAGAGAC__GGTTTCATTATGTTGCCCAGGCTGGTCTCGA CAG C NR2C2 Ensembl:ENSG00000177463 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1295815426 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_216097,RMVar_hsa_circ_371945,RMVar_hsa_circ_343621,RMVar_hsa_circ_123808,RMVar_hsa_circ_216105,RMVar_hsa_circ_295747,RMVar_hsa_circ_216095,RMVar_hsa_circ_216096,RMVar_hsa_circ_373433,RMVar_hsa_circ_311004,RMVar_hsa_circ_54468,RMVar_hsa_circ_216103,RMVar_hsa_circ_216104,RMVar_hsa_circ_307390,RMVar_hsa_circ_36715,RMVar_hsa_circ_216112,RMVar_hsa_circ_8100,RMVar_hsa_circ_293590,RMVar_hsa_circ_309201,RMVar_hsa_circ_216118,RMVar_hsa_circ_288953,RMVar_hsa_circ_36064,RMVar_hsa_circ_216120 6226 RMVar_ID_6226 Human_SNP_ID_123753538 A-to-I Human chr3 + 15035840 15035840 15035840 CCTGAGCTTGGGCGTTCGAAACCAGCCTGGGCAACATGGCGAAACCTCGTCTCTACTAAAAATAC CCTGAGCTTGGGCGTTCGAAACCAGCCTGGGCTACATGGCGAAACCTCGTCTCTACTAAAAATAC A T NR2C2 Ensembl:ENSG00000177463 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1047437749 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_371945,RMVar_hsa_circ_343621,RMVar_hsa_circ_295747,RMVar_hsa_circ_216095,RMVar_hsa_circ_216096,RMVar_hsa_circ_54468,RMVar_hsa_circ_216103,RMVar_hsa_circ_36715,RMVar_hsa_circ_8100,RMVar_hsa_circ_309201,RMVar_hsa_circ_369123,RMVar_hsa_circ_216122 6227 RMVar_ID_6227 Human_SNP_ID_123753735 A-to-I Human chr3 + 15036567 15036567 15036567 AGGCTGGAGTGCAGTAGCAATCATAGCTCACTACAGCCTTGAACCCCTGGGCTCAAGTGATCCTC AGGCTGGAGTGCAGTAGCAATCATAGCTCACTGCAGCCTTGAACCCCTGGGCTCAAGTGATCCTC A G NR2C2 Ensembl:ENSG00000177463 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs890309191 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_371945,RMVar_hsa_circ_343621,RMVar_hsa_circ_295747,RMVar_hsa_circ_216095,RMVar_hsa_circ_216096,RMVar_hsa_circ_54468,RMVar_hsa_circ_216103,RMVar_hsa_circ_36715,RMVar_hsa_circ_8100,RMVar_hsa_circ_309201,RMVar_hsa_circ_369123,RMVar_hsa_circ_216122 6228 RMVar_ID_6228 Human_SNP_ID_123753767 A-to-I Human chr3 + 15036663 15036663 15036663 CAGGCATGTGCCATCACACCCAGATAATTTTTATATTTTTTAATAGAGATGAGGTTTCGCTGTGC CAGGCATGTGCCATCACACCCAGATAATTTTTGTATTTTTTAATAGAGATGAGGTTTCGCTGTGC A G NR2C2 Ensembl:ENSG00000177463 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs750495425 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_371945,RMVar_hsa_circ_343621,RMVar_hsa_circ_295747,RMVar_hsa_circ_216095,RMVar_hsa_circ_216096,RMVar_hsa_circ_54468,RMVar_hsa_circ_216103,RMVar_hsa_circ_36715,RMVar_hsa_circ_8100,RMVar_hsa_circ_309201,RMVar_hsa_circ_369123,RMVar_hsa_circ_216122 6229 RMVar_ID_6229 Human_SNP_ID_123759004 A-to-I Human chr3 - 15055951 15055951 15055951 CCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGCGTCCGGCCTGAAGCTTTTCCA CCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCGTCCGGCCTGAAGCTTTTCCA T C MRPS25 Ensembl:ENSG00000131368 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs368170245 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14674095 6230 RMVar_ID_6230 Human_SNP_ID_123759099 A-to-I Human chr3 - 15056209 15056209 15056209 CAGTCTGTTTGAATCTTTTTTTTTTTTGAGACAGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCA CAGTCTGTTTGAATCTTTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCA T C MRPS25 Ensembl:ENSG00000131368 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569976372 Functional Loss SNV dbSNP153 33..33 33 - - - 6231 RMVar_ID_6231 Human_SNP_ID_123759525 A-to-I Human chr3 - 15057945 15057945 15057945 GGGAGGCAGAGGTTGCAGTGAGCCAAGATCGCACCACTGCACGCCAGCCTGGGCAACAGAGTGAG GGGAGGCAGAGGTTGCAGTGAGCCAAGATCGCGCCACTGCACGCCAGCCTGGGCAACAGAGTGAG T C MRPS25 Ensembl:ENSG00000131368 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264779861 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25705348 6232 RMVar_ID_6232 Human_SNP_ID_123759529 A-to-I Human chr3 - 15057953 15057953 15057953 TTGAGCCTGGGAGGCAGAGGTTGCAGTGAGCCAAGATCGCACCACTGCACGCCAGCCTGGGCAAC TTGAGCCTGGGAGGCAGAGGTTGCAGTGAGCCGAGATCGCACCACTGCACGCCAGCCTGGGCAAC T C MRPS25 Ensembl:ENSG00000131368 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1479909429 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25767311 6233 RMVar_ID_6233 Human_SNP_ID_123759533 A-to-I Human chr3 - 15057970 15057969 15057970 GGCTGAGGCAGGATTGCTTGAGCCTGGGAGGCAGAGGTTGCAGTGAGCCAAGATCGCACCACTGC GGCTGAGGCAGGATTGCTTGAGCCTGGGAGGC_GAGGTTGCAGTGAGCCAAGATCGCACCACTGC CT C MRPS25 Ensembl:ENSG00000131368 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs534149734 Functional Loss DEL dbSNP153 33..33 33 - - - 6234 RMVar_ID_6234 Human_SNP_ID_123759534 A-to-I Human chr3 - 15057970 15057970 15057970 GGCTGAGGCAGGATTGCTTGAGCCTGGGAGGCAGAGGTTGCAGTGAGCCAAGATCGCACCACTGC GGCTGAGGCAGGATTGCTTGAGCCTGGGAGGCGGAGGTTGCAGTGAGCCAAGATCGCACCACTGC T C MRPS25 Ensembl:ENSG00000131368 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1471198524 Functional Loss SNV dbSNP153 33..33 33 - - - 6235 RMVar_ID_6235 Human_SNP_ID_123759565 A-to-I Human chr3 - 15058155 15058155 15058155 AGTGCTGTGGGCCTGGTGGCACAGTGGCTCACACCTGTAATCCCAGTACTTTGGGAGGCTGAAGA AGTGCTGTGGGCCTGGTGGCACAGTGGCTCACGCCTGTAATCCCAGTACTTTGGGAGGCTGAAGA T C MRPS25 Ensembl:ENSG00000131368 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1283412932 Functional Loss SNV dbSNP153 33..33 33 - - - 6236 RMVar_ID_6236 Human_SNP_ID_123763595 A-to-I Human chr3 - 15072209 15072209 15072209 CTCTGTATTTTTAGTAGAGGTAGAGTTTCACCATTTTGGCCAGGCTGGTTTCGAACTCCTGGCCT CTCTGTATTTTTAGTAGAGGTAGAGTTTCACCGTTTTGGCCAGGCTGGTTTCGAACTCCTGGCCT T C RBSN Ensembl:ENSG00000131381 Protein coding 3'UTR GSE38233;GSE99789;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29796672,32596459 RNA-Seq:(High) rs900146852 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14674802 RMVar_hsa_circ_100635,RMVar_hsa_circ_216128 6237 RMVar_ID_6237 Human_SNP_ID_123763620 A-to-I Human chr3 - 15072270 15072270 15072270 TTTGTGCCTCAGCCCCCTGAATAGCTAGGATTACAGGCGTGGGCCACCACGCCTGGTTAATCTCT TTTGTGCCTCAGCCCCCTGAATAGCTAGGATTGCAGGCGTGGGCCACCACGCCTGGTTAATCTCT T C RBSN Ensembl:ENSG00000131381 Protein coding 3'UTR GSE38233;GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,32596459,32596459 RNA-Seq:(High) rs1356119681 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100635,RMVar_hsa_circ_216128 6238 RMVar_ID_6238 Human_SNP_ID_123763647 A-to-I Human chr3 - 15072386 15072386 15072386 GCACTGATGAGATTTTTTATTTTTTTTGAGACAGAGTTTCACTTTGTTGCCCAGGCTGGAGTGTA GCACTGATGAGATTTTTTATTTTTTTTGAGACCGAGTTTCACTTTGTTGCCCAGGCTGGAGTGTA T G RBSN Ensembl:ENSG00000131381 Protein coding 3'UTR GSE38233;GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;ASD brains,temporal_cortex;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,30559470,31158229,32596459 RNA-Seq:(High) rs927999690 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100635,RMVar_hsa_circ_216128 6239 RMVar_ID_6239 Human_SNP_ID_123763730 A-to-I Human chr3 - 15072746 15072746 15072746 TCGCACCACTGCACTCCAGCCTGGGCAGTGAGAGTGAGACTCCGTCTCAAAAAAAAATAAGAGTG TCGCACCACTGCACTCCAGCCTGGGCAGTGAGGGTGAGACTCCGTCTCAAAAAAAAATAAGAGTG T C RBSN Ensembl:ENSG00000131381 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs905485975 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100635,RMVar_hsa_circ_216128 6240 RMVar_ID_6240 Human_SNP_ID_123799209 A-to-I Human chr3 + 15214580 15214580 15214580 ACCCCTACAAAAATTGAAAAAATTTGCTGGGCATGGTGGTGTGTGCCTGTAGTCCCAGCTCCTCA ACCCCTACAAAAATTGAAAAAATTTGCTGGGCGTGGTGGTGTGTGCCTGTAGTCCCAGCTCCTCA A G CAPN7 Ensembl:ENSG00000131375 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs997014052 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60347,RMVar_hsa_circ_84590,RMVar_hsa_circ_279852,RMVar_hsa_circ_344278,RMVar_hsa_circ_216138,RMVar_hsa_circ_352969,RMVar_hsa_circ_353163,RMVar_hsa_circ_283828,RMVar_hsa_circ_307466,RMVar_hsa_circ_282445,RMVar_hsa_circ_268990,RMVar_hsa_circ_278745,RMVar_hsa_circ_65298,RMVar_hsa_circ_216140,RMVar_hsa_circ_216142,RMVar_hsa_circ_57751,RMVar_hsa_circ_216143,RMVar_hsa_circ_216141,RMVar_hsa_circ_216139 6241 RMVar_ID_6241 Human_SNP_ID_123799547 A-to-I Human chr3 + 15215822 15215822 15215822 AGTTAAGAACATTCATGTACACGCAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAG AGTTAAGAACATTCATGTACACGCAGTGGCTCGTGCCTGTAATCCCAGCACTTTGGGAGGCCAAG A G CAPN7 Ensembl:ENSG00000131375 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1427439554 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60347,RMVar_hsa_circ_84590,RMVar_hsa_circ_279852,RMVar_hsa_circ_344278,RMVar_hsa_circ_216138,RMVar_hsa_circ_352969,RMVar_hsa_circ_353163,RMVar_hsa_circ_283828,RMVar_hsa_circ_307466,RMVar_hsa_circ_282445,RMVar_hsa_circ_268990,RMVar_hsa_circ_278745,RMVar_hsa_circ_65298,RMVar_hsa_circ_216140,RMVar_hsa_circ_216142,RMVar_hsa_circ_57751,RMVar_hsa_circ_216143,RMVar_hsa_circ_216141,RMVar_hsa_circ_216139 6242 RMVar_ID_6242 Human_SNP_ID_123799549 A-to-I Human chr3 + 15215830 15215830 15215830 ACATTCATGTACACGCAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGACAG ACATTCATGTACACGCAGTGGCTCATGCCTGTGATCCCAGCACTTTGGGAGGCCAAGGCAGACAG A G CAPN7 Ensembl:ENSG00000131375 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs528513736 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60347,RMVar_hsa_circ_84590,RMVar_hsa_circ_279852,RMVar_hsa_circ_344278,RMVar_hsa_circ_216138,RMVar_hsa_circ_352969,RMVar_hsa_circ_353163,RMVar_hsa_circ_283828,RMVar_hsa_circ_307466,RMVar_hsa_circ_282445,RMVar_hsa_circ_268990,RMVar_hsa_circ_278745,RMVar_hsa_circ_65298,RMVar_hsa_circ_216140,RMVar_hsa_circ_216142,RMVar_hsa_circ_57751,RMVar_hsa_circ_216143,RMVar_hsa_circ_216141,RMVar_hsa_circ_216139 6243 RMVar_ID_6243 Human_SNP_ID_123815897 A-to-I Human chr3 - 15274626 15274626 15274626 GTCCAGTGGTGGTGGCATGGACCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATTACT GTCCAGTGGTGGTGGCATGGACCTGTAGTCCCCGCTACTCAGGAGGCTGAGGCAGGAGAATTACT T G SH3BP5 Ensembl:ENSG00000131370 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432540129 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_216169,RMVar_hsa_circ_369940,RMVar_hsa_circ_315080 6244 RMVar_ID_6244 Human_SNP_ID_123825289 A-to-I Human chr3 - 15311959 15311959 15311959 ACTGGACTACAAGACTGAAGATGGCTGGTTGCAGTGGCTCACGCCTGTAATCACAACAGTTTGGG ACTGGACTACAAGACTGAAGATGGCTGGTTGCGGTGGCTCACGCCTGTAATCACAACAGTTTGGG T C SH3BP5 Ensembl:ENSG00000131370 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs553438040 Functional Loss SNV dbSNP153 33..33 33 - - - 6245 RMVar_ID_6245 Human_SNP_ID_123842255 A-to-I Human chr3 - 15382196 15382196 15382196 GACTAATGAAAAGTGGCCGGGCACAGATGCTCATGCCTATAATCCCAGCACTTCGGGAGGGTGAG GACTAATGAAAAGTGGCCGGGCACAGATGCTCGTGCCTATAATCCCAGCACTTCGGGAGGGTGAG T C METTL6 Ensembl:ENSG00000206562 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs913306274 Functional Loss SNV dbSNP153 33..33 33 - - - 6246 RMVar_ID_6246 Human_SNP_ID_123842795 A-to-I Human chr3 - 15384577 15384577 15384577 GTGCCATCACACCCAACTAATTTTTTTTTCTTACAGAGAGATGGTCTCGCTATGTTGCCCAGGCT GTGCCATCACACCCAACTAATTTTTTTTTCTTGCAGAGAGATGGTCTCGCTATGTTGCCCAGGCT T C METTL6 Ensembl:ENSG00000206562 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1263038418 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_398645 6247 RMVar_ID_6247 Human_SNP_ID_123849551 A-to-I Human chr3 - 15410334 15410332 15410335 TGGGCGACAGAGCAAAAGTCTGTCTCAAAAAAAACAAAAAAAATTTGAAAGATCACATTCACATA TGGGCGACAGAGCAAAAGTCTGTCTCAAAAA___CAAAAAAAATTTGAAAGATCACATTCACATA GTTT G METTL6 Ensembl:ENSG00000206562 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs372175784 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_10073500,Human_RBP_ID_25767447 6248 RMVar_ID_6248 Human_SNP_ID_123849555 A-to-I Human chr3 - 15410334 15410334 15410334 TGGGCGACAGAGCAAAAGTCTGTCTCAAAAAAAACAAAAAAAATTTGAAAGATCACATTCACATA TGGGCGACAGAGCAAAAGTCTGTCTCAAAAAAGACAAAAAAAATTTGAAAGATCACATTCACATA T C METTL6 Ensembl:ENSG00000206562 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1312367165 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10073500,Human_RBP_ID_25767447 6249 RMVar_ID_6249 Human_SNP_ID_123849572 A-to-I Human chr3 - 15410390 15410390 15410390 TGAGCCTGGAAGGTGGAGGTTGCAGTAAGTCGAGATCACGCTACTGCACTCCAGCCTGGGCGACA TGAGCCTGGAAGGTGGAGGTTGCAGTAAGTCGTGATCACGCTACTGCACTCCAGCCTGGGCGACA T A METTL6 Ensembl:ENSG00000206562 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1259822415 Functional Loss SNV dbSNP153 33..33 33 - - - 6250 RMVar_ID_6250 Human_SNP_ID_123849590 A-to-I Human chr3 - 15410470 15410470 15410470 TCTGTCTCTACAGAAAATACAAAAATTAGCCAAATGTGGTGGCATGTGCCTGTAGTCCCAGCTGG TCTGTCTCTACAGAAAATACAAAAATTAGCCATATGTGGTGGCATGTGCCTGTAGTCCCAGCTGG T A METTL6 Ensembl:ENSG00000206562 Protein coding intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs759562322 Functional Loss SNV dbSNP153 33..33 33 - - - 6251 RMVar_ID_6251 Human_SNP_ID_123849683 A-to-I Human chr3 - 15410851 15410851 15410851 TTTATATATTTTTTGAGACAGGATCTTGTGGTACGCAGGCTGGAGTGCAGTGGTGTGTGATCACA TTTATATATTTTTTGAGACAGGATCTTGTGGTGCGCAGGCTGGAGTGCAGTGGTGTGTGATCACA T C METTL6 Ensembl:ENSG00000206562 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1465849842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14682772,Human_RBP_ID_26510100 6252 RMVar_ID_6252 Human_SNP_ID_123849960 A-to-I Human chr3 - 15411914 15411914 15411914 CTAAAAATACAAAAAAATTAACCAGGCATGGTAGTGTGTGCCTGTAGTCCCAGCTACTTAAGAGG CTAAAAATACAAAAAAATTAACCAGGCATGGTCGTGTGTGCCTGTAGTCCCAGCTACTTAAGAGG T G METTL6 Ensembl:ENSG00000206562 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,31158229,31158229 RNA-Seq:(High) rs1476130957 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_274004,RMVar_hsa_circ_271125,RMVar_hsa_circ_216172,RMVar_hsa_circ_216173 6253 RMVar_ID_6253 Human_SNP_ID_123850131 A-to-I Human chr3 - 15412547 15412547 15412547 CCAGAAGATGGAGGCTGCAGTGAGCTATGATCATACCACTGCCCTCCAGCCTGGGCGACAGGGCG CCAGAAGATGGAGGCTGCAGTGAGCTATGATCGTACCACTGCCCTCCAGCCTGGGCGACAGGGCG T C METTL6 Ensembl:ENSG00000206562 Protein coding intron GSE38233;GSE107867 cultured B-cells;ASD brains,frontal_cortex - 24183664,30559470 RNA-Seq:(High) rs1230828617 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_274004,RMVar_hsa_circ_271125,RMVar_hsa_circ_216172,RMVar_hsa_circ_216173 6254 RMVar_ID_6254 Human_SNP_ID_123850157 A-to-I Human chr3 - 15412648 15412648 15412648 GTCTCTACTAAAAATAAAAAAAAAAAAATATTAGCCAGGAGTGGTGGCATGCACTTGTGGTCCTG GTCTCTACTAAAAATAAAAAAAAAAAAATATTTGCCAGGAGTGGTGGCATGCACTTGTGGTCCTG T A METTL6 Ensembl:ENSG00000206562 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1198541673 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25706826 RMVar_hsa_circ_274004,RMVar_hsa_circ_271125,RMVar_hsa_circ_216172,RMVar_hsa_circ_216173 6255 RMVar_ID_6255 Human_SNP_ID_123850196 A-to-I Human chr3 - 15412733 15412733 15412733 AGCTGCAAAATTATTTGGGAGACTGAGATAGAAGGATCACTTGAGCTCAGGAGTTCGAGACCAGC AGCTGCAAAATTATTTGGGAGACTGAGATAGATGGATCACTTGAGCTCAGGAGTTCGAGACCAGC T A METTL6 Ensembl:ENSG00000206562 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs927857514 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14682815 RMVar_hsa_circ_274004,RMVar_hsa_circ_271125,RMVar_hsa_circ_216172,RMVar_hsa_circ_216173 6256 RMVar_ID_6256 Human_SNP_ID_123850282 A-to-I Human chr3 - 15413133 15413133 15413133 TCAAGTGATTCTCATGCCTCAGCCTCCCAAGTAGCAAGGATTACAAGTGTGTGCCACCACACCCA TCAAGTGATTCTCATGCCTCAGCCTCCCAAGTGGCAAGGATTACAAGTGTGTGCCACCACACCCA T C METTL6 Ensembl:ENSG00000206562 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs950788890 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_274004,RMVar_hsa_circ_271125,RMVar_hsa_circ_216172,RMVar_hsa_circ_216173 6257 RMVar_ID_6257 Human_SNP_ID_123850362 A-to-I Human chr3 - 15413510 15413510 15413510 TGGAGTGCAGTGGTGTGATCTTGGCTCACTGCAGCCTCCACCTTCCAGACTCAAGTGATCCACCG TGGAGTGCAGTGGTGTGATCTTGGCTCACTGCGGCCTCCACCTTCCAGACTCAAGTGATCCACCG T C METTL6 Ensembl:ENSG00000206562 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1259596386 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_274004,RMVar_hsa_circ_271125,RMVar_hsa_circ_216172,RMVar_hsa_circ_216173 6258 RMVar_ID_6258 Human_SNP_ID_123850382 A-to-I Human chr3 - 15413566 15413566 15413566 TTGGGGTTTGGTTTTTTTGTTGTTTTTGAGACAGAGTCTAATTCTGTCACCCAGGCTGGAGTGCA TTGGGGTTTGGTTTTTTTGTTGTTTTTGAGACGGAGTCTAATTCTGTCACCCAGGCTGGAGTGCA T C METTL6 Ensembl:ENSG00000206562 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1051545577 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7141469,Human_RBP_ID_14682828 RMVar_hsa_circ_274004,RMVar_hsa_circ_271125,RMVar_hsa_circ_216172,RMVar_hsa_circ_216173 6259 RMVar_ID_6259 Human_SNP_ID_123850671 A-to-I Human chr3 - 15414493 15414493 15414493 AAATTAGCCGGGCATGGTGGCGGGCACCTATAATCCCAGCTACTCGGGAGGCTGAGACACGAGAA AAATTAGCCGGGCATGGTGGCGGGCACCTATAGTCCCAGCTACTCGGGAGGCTGAGACACGAGAA T C METTL6 Ensembl:ENSG00000206562 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1212746650 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_274004,RMVar_hsa_circ_216172,RMVar_hsa_circ_216175,RMVar_hsa_circ_275726,RMVar_hsa_circ_301705,RMVar_hsa_circ_216174 6260 RMVar_ID_6260 Human_SNP_ID_123850673 A-to-I Human chr3 - 15414496 15414496 15414496 CAAAAATTAGCCGGGCATGGTGGCGGGCACCTATAATCCCAGCTACTCGGGAGGCTGAGACACGA CAAAAATTAGCCGGGCATGGTGGCGGGCACCTGTAATCCCAGCTACTCGGGAGGCTGAGACACGA T C METTL6 Ensembl:ENSG00000206562 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1279905999 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_274004,RMVar_hsa_circ_216172,RMVar_hsa_circ_216175,RMVar_hsa_circ_275726,RMVar_hsa_circ_301705,RMVar_hsa_circ_216174 6261 RMVar_ID_6261 Human_SNP_ID_123850727 A-to-I Human chr3 - 15414738 15414738 15414738 TTAATTTTTGTGTAGAGATGGGGTCTCACTATATTGCCCAGGTTGGTCTCTAACATTTTAATCCT TTAATTTTTGTGTAGAGATGGGGTCTCACTATGTTGCCCAGGTTGGTCTCTAACATTTTAATCCT T C METTL6 Ensembl:ENSG00000206562 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1400059980 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17573526 Human_Splice_Rec_398681 RMVar_hsa_circ_274004,RMVar_hsa_circ_216172,RMVar_hsa_circ_216175,RMVar_hsa_circ_275726,RMVar_hsa_circ_301705,RMVar_hsa_circ_216174 6262 RMVar_ID_6262 Human_SNP_ID_123850744 A-to-I Human chr3 - 15414800 15414800 15414800 CTCCCACCTCAGCCTCTGAAGTAGTTGGGACTACAGGACGCACTACCAGATCCAGCTAATTTTTA CTCCCACCTCAGCCTCTGAAGTAGTTGGGACTGCAGGACGCACTACCAGATCCAGCTAATTTTTA T C METTL6 Ensembl:ENSG00000206562 Protein coding intron GSE38233;GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,32596459 RNA-Seq:(High) rs1441028809 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14682866 Human_Splice_Rec_398681 RMVar_hsa_circ_274004,RMVar_hsa_circ_216172,RMVar_hsa_circ_216175,RMVar_hsa_circ_275726,RMVar_hsa_circ_301705,RMVar_hsa_circ_216174 6263 RMVar_ID_6263 Human_SNP_ID_123850774 A-to-I Human chr3 - 15414900 15414900 15414900 TATTTATTTTTGAGACAGGGTCTTGCTGTGTCACTCAGGCTGGAGTGCAGTGGCATGGACGTGGC TATTTATTTTTGAGACAGGGTCTTGCTGTGTCGCTCAGGCTGGAGTGCAGTGGCATGGACGTGGC T C METTL6 Ensembl:ENSG00000206562 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1301748850 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_398680,Human_Splice_Rec_398700 RMVar_hsa_circ_274004,RMVar_hsa_circ_216172,RMVar_hsa_circ_216175,RMVar_hsa_circ_275726,RMVar_hsa_circ_301705,RMVar_hsa_circ_216174 6264 RMVar_ID_6264 Human_SNP_ID_123908155 A-to-I Human chr3 + 15642960 15642960 15642960 TGAGGCAGGAGAATCACTTGAACCTGGGAGGCAGGAGTTGCGGTGAGAAAGATCGCGCCACTGCA TGAGGCAGGAGAATCACTTGAACCTGGGAGGCGGGAGTTGCGGTGAGAAAGATCGCGCCACTGCA A G BTD Ensembl:ENSG00000169814 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1007771171 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87295,RMVar_hsa_circ_216208 6265 RMVar_ID_6265 Human_SNP_ID_123917956 A-to-I Human chr3 - 15681172 15681172 15681172 AAGTTGTAAGTAATCTAGAGATGACTTAAAGTATATGAGAAGATGTGCATAGGTTATACACAAAT AAGTTGTAAGTAATCTAGAGATGACTTAAAGTGTATGAGAAGATGTGCATAGGTTATACACAAAT T C ANKRD28 Ensembl:ENSG00000206560 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1435092844 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2409,RMVar_hsa_circ_269508,RMVar_hsa_circ_363026,RMVar_hsa_circ_58632,RMVar_hsa_circ_369600,RMVar_hsa_circ_313904,RMVar_hsa_circ_39792,RMVar_hsa_circ_86013,RMVar_hsa_circ_268633,RMVar_hsa_circ_17449,RMVar_hsa_circ_34667,RMVar_hsa_circ_216213,RMVar_hsa_circ_216214,RMVar_hsa_circ_216212,RMVar_hsa_circ_41108,RMVar_hsa_circ_371894,RMVar_hsa_circ_39536,RMVar_hsa_circ_52942,RMVar_hsa_circ_216216,RMVar_hsa_circ_216215,RMVar_hsa_circ_378599,RMVar_hsa_circ_30615,RMVar_hsa_circ_216218,RMVar_hsa_circ_1810,RMVar_hsa_circ_326230,RMVar_hsa_circ_216220 6266 RMVar_ID_6266 Human_SNP_ID_123920169 A-to-I Human chr3 - 15690693 15690693 15690693 GGGCATGGTGACGTGTACCTCTGGTCCCTGCTACTCAGGAGGCTGAGGTGGGAGGATCACTTAAG GGGCATGGTGACGTGTACCTCTGGTCCCTGCTCCTCAGGAGGCTGAGGTGGGAGGATCACTTAAG T G ANKRD28 Ensembl:ENSG00000206560 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1308400974 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2409,RMVar_hsa_circ_58632,RMVar_hsa_circ_369600,RMVar_hsa_circ_39792,RMVar_hsa_circ_268633,RMVar_hsa_circ_17449,RMVar_hsa_circ_34667,RMVar_hsa_circ_216214,RMVar_hsa_circ_41108,RMVar_hsa_circ_10027,RMVar_hsa_circ_82297,RMVar_hsa_circ_52942,RMVar_hsa_circ_216215,RMVar_hsa_circ_313816,RMVar_hsa_circ_365997,RMVar_hsa_circ_127368,RMVar_hsa_circ_125450,RMVar_hsa_circ_216221,RMVar_hsa_circ_216223,RMVar_hsa_circ_216224,RMVar_hsa_circ_216222,RMVar_hsa_circ_59797,RMVar_hsa_circ_91525,RMVar_hsa_circ_108502,RMVar_hsa_circ_216227,RMVar_hsa_circ_318189,RMVar_hsa_circ_72612,RMVar_hsa_circ_216228 6267 RMVar_ID_6267 Human_SNP_ID_123950103 A-to-I Human chr3 - 15811942 15811942 15811942 TGCTGTGTTGGCCAGACTGGTCTTGAACTCCTAACTGAAGTGATCCACCCACCTTGACCTCCCAA TGCTGTGTTGGCCAGACTGGTCTTGAACTCCTGACTGAAGTGATCCACCCACCTTGACCTCCCAA T C ANKRD28 Ensembl:ENSG00000206560 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1471191373 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100377,RMVar_hsa_circ_216231,RMVar_hsa_circ_216240,RMVar_hsa_circ_335396,RMVar_hsa_circ_291183,RMVar_hsa_circ_216252,RMVar_hsa_circ_216255,RMVar_hsa_circ_302918,RMVar_hsa_circ_216254,RMVar_hsa_circ_216256,RMVar_hsa_circ_291096 6268 RMVar_ID_6268 Human_SNP_ID_123955277 A-to-I Human chr3 - 15834058 15834058 15834058 AGACAATTTTAAAAAAGCTTTCACACAGTAAAAGAAACAGTGAACAGAGTAAACATACAACCTAC AGACAATTTTAAAAAAGCTTTCACACAGTAAATGAAACAGTGAACAGAGTAAACATACAACCTAC T A ANKRD28 Ensembl:ENSG00000206560 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs980590988 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100377,RMVar_hsa_circ_216231 6269 RMVar_ID_6269 Human_SNP_ID_123957160 A-to-I Human chr3 - 15841884 15841884 15841884 CTGGATCATATGGTAGTGCTAGTGCCATTTTTAGTTTTTTGAGGAACCTCCAAACTGTTCTCCCT CTGGATCATATGGTAGTGCTAGTGCCATTTTTGGTTTTTTGAGGAACCTCCAAACTGTTCTCCCT T C ANKRD28 Ensembl:ENSG00000206560 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1050551785 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100377,RMVar_hsa_circ_216231 6270 RMVar_ID_6270 Human_SNP_ID_124087194 A-to-I Human chr3 - 16378006 16378006 16378006 TGAACTCGGCAGGCAGCAGTGCTCCGGTGTCTACTGCCAACAGCACCGAGGATGCCAGAGATGCA TGAACTCGGCAGGCAGCAGTGCTCCGGTGTCTGCTGCCAACAGCACCGAGGATGCCAGAGATGCA T C RFTN1 Ensembl:ENSG00000131378 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1366795814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_399840,Human_Splice_Rec_399858,Human_Splice_Rec_399884,Human_Splice_Rec_399890,Human_Splice_Rec_399896,Human_Splice_Rec_399904,Human_Splice_Rec_399912,Human_Splice_Rec_399920 Human_miRNA_ID_2584800 RMVar_hsa_circ_89779,RMVar_hsa_circ_216280,RMVar_hsa_circ_216283,RMVar_hsa_circ_84793,RMVar_hsa_circ_338575,RMVar_hsa_circ_216282,RMVar_hsa_circ_334487,RMVar_hsa_circ_216284,RMVar_hsa_circ_30348,RMVar_hsa_circ_357427 6271 RMVar_ID_6271 Human_SNP_ID_124236738 A-to-I Human chr3 + 16986433 16986433 16986433 TTCTTTTTTTCTTTCTTGAAAGACAAGATCTCACTCTGTCATCCAGGCTGGAATGCAGTGGCATG TTCTTTTTTTCTTTCTTGAAAGACAAGATCTCGCTCTGTCATCCAGGCTGGAATGCAGTGGCATG A G PLCL2 Ensembl:ENSG00000154822 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs774518252 Functional Loss SNV dbSNP153 33..33 33 - - - 6272 RMVar_ID_6272 Human_SNP_ID_124287334 A-to-I Human chr3 - 17197514 17197514 17197514 AAATTAGCTGGGCTTGGTGGCACACACCTGTAATTCTAGCTATTTGGGAGGTTGAGGTGAAAAGA AAATTAGCTGGGCTTGGTGGCACACACCTGTAGTTCTAGCTATTTGGGAGGTTGAGGTGAAAAGA T C TBC1D5 Ensembl:ENSG00000131374 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs940101081 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93803,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_14947,RMVar_hsa_circ_299946,RMVar_hsa_circ_97576,RMVar_hsa_circ_216300,RMVar_hsa_circ_216301,RMVar_hsa_circ_303689,RMVar_hsa_circ_71316,RMVar_hsa_circ_274749,RMVar_hsa_circ_64117,RMVar_hsa_circ_216302,RMVar_hsa_circ_216303 6273 RMVar_ID_6273 Human_SNP_ID_124300760 A-to-I Human chr3 - 17255849 17255849 17255849 TGTATTTTTAGTAGACGGGGTTTCACCGTGTTAGCCAAGATGGTCTCAATCTCCTGACCTCGTGA TGTATTTTTAGTAGACGGGGTTTCACCGTGTTGGCCAAGATGGTCTCAATCTCCTGACCTCGTGA T C TBC1D5 Ensembl:ENSG00000131374 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs562576107 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1898,RMVar_hsa_circ_93803,RMVar_hsa_circ_118271,RMVar_hsa_circ_115931,RMVar_hsa_circ_216299,RMVar_hsa_circ_216298,RMVar_hsa_circ_14947,RMVar_hsa_circ_299946,RMVar_hsa_circ_97576,RMVar_hsa_circ_216300,RMVar_hsa_circ_216301,RMVar_hsa_circ_71316,RMVar_hsa_circ_216305,RMVar_hsa_circ_298666,RMVar_hsa_circ_302564,RMVar_hsa_circ_352952,RMVar_hsa_circ_18487,RMVar_hsa_circ_328839,RMVar_hsa_circ_43371,RMVar_hsa_circ_266713,RMVar_hsa_circ_216306,RMVar_hsa_circ_366472,RMVar_hsa_circ_71033,RMVar_hsa_circ_316820,RMVar_hsa_circ_216308,RMVar_hsa_circ_216307 6274 RMVar_ID_6274 Human_SNP_ID_124413046 A-to-I Human chr3 - 17709594 17709593 17709594 GAATCATTATTATTTCAATGTGCCGTTAGACAAGGTTCTTTGAATGCCAGTAACAGAAACCCATA GAATCATTATTATTTCAATGTGCCGTTAGACA_GGTTCTTTGAATGCCAGTAACAGAAACCCATA CT C TBC1D5 Ensembl:ENSG00000131374 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs943599788 Functional Loss DEL dbSNP153 33..33 33 - - - 6275 RMVar_ID_6275 Human_SNP_ID_124413048 A-to-I Human chr3 - 17709599 17709599 17709599 CAGTGGAATCATTATTATTTCAATGTGCCGTTAGACAAGGTTCTTTGAATGCCAGTAACAGAAAC CAGTGGAATCATTATTATTTCAATGTGCCGTTGGACAAGGTTCTTTGAATGCCAGTAACAGAAAC T C TBC1D5 Ensembl:ENSG00000131374 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973491057 Functional Loss SNV dbSNP153 33..33 33 - - - 6276 RMVar_ID_6276 Human_SNP_ID_124416605 A-to-I Human chr3 - 17724185 17724185 17724185 CCATAGGCACAGCCATTTGGGAGACTGAGGCTAGAGGATTGCTTGAGCCCAGTGAGGCTGCAGTG CCATAGGCACAGCCATTTGGGAGACTGAGGCTGGAGGATTGCTTGAGCCCAGTGAGGCTGCAGTG T C TBC1D5 Ensembl:ENSG00000131374 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913858608 Functional Loss SNV dbSNP153 33..33 33 - - - 6277 RMVar_ID_6277 Human_SNP_ID_124453282 A-to-I Human chr3 - 17872069 17872069 17872069 AGCCAATTGTAATGATATCAATGATGTCAAACAGCTGAAACCTGGCTACTTAGAAGCTACTGTGG AGCCAATTGTAATGATATCAATGATGTCAAACGGCTGAAACCTGGCTACTTAGAAGCTACTGTGG T C TBC1D5,AC104297.1 Ensembl:ENSG00000131374,Ensembl:ENSG00000213383 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879096660 Functional Loss SNV dbSNP153 33..33 33 - - - 6278 RMVar_ID_6278 Human_SNP_ID_124453291 A-to-I Human chr3 - 17872116 17872116 17872116 GAAACTAACTGGAAAGTCATTGCCATCAATGTAGATGATCCTGATGCAGCCAATTGTAATGATAT GAAACTAACTGGAAAGTCATTGCCATCAATGTGGATGATCCTGATGCAGCCAATTGTAATGATAT T C TBC1D5,AC104297.1 Ensembl:ENSG00000131374,Ensembl:ENSG00000213383 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878943392 Functional Loss SNV dbSNP153 33..33 33 - - - 6279 RMVar_ID_6279 Human_SNP_ID_124612426 A-to-I Human chr3 - 18538932 18538932 18538932 TGCTGGCAGGAGCTGACTGCTGAGTTGTAGCTAGTGCTGGTGTGGACACTGCTTTGGGTTCGGTC TGCTGGCAGGAGCTGACTGCTGAGTTGTAGCTGGTGCTGGTGTGGACACTGCTTTGGGTTCGGTC T C - - Other Unknown GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs779219867 Functional Loss SNV dbSNP153 33..33 33 - - - 6280 RMVar_ID_6280 Human_SNP_ID_124966565 A-to-I Human chr3 - 19936228 19936228 19936228 CTCCCACTTCAGCCTCTCAGATAGCTGAGACTACAGATGTGAGCCACCACGCTGGGCTAATTGAA CTCCCACTTCAGCCTCTCAGATAGCTGAGACTTCAGATGTGAGCCACCACGCTGGGCTAATTGAA T A EFHB Ensembl:ENSG00000163576 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251515448 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_401331 6281 RMVar_ID_6281 Human_SNP_ID_124966566 A-to-I Human chr3 - 19936228 19936228 19936228 CTCCCACTTCAGCCTCTCAGATAGCTGAGACTACAGATGTGAGCCACCACGCTGGGCTAATTGAA CTCCCACTTCAGCCTCTCAGATAGCTGAGACTGCAGATGTGAGCCACCACGCTGGGCTAATTGAA T C EFHB Ensembl:ENSG00000163576 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251515448 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_401331 6282 RMVar_ID_6282 Human_SNP_ID_124969755 A-to-I Human chr3 - 19947381 19947381 19947381 GCGTCGCCTGCTCTTAGCGCCGCTCCCCTCACACTGGACTGTGCGGGGCTCGTGCCGTGGTGCCG GCGTCGCCTGCTCTTAGCGCCGCTCCCCTCACGCTGGACTGTGCGGGGCTCGTGCCGTGGTGCCG T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs565563133 Functional Loss SNV dbSNP153 33..33 33 - - - 6283 RMVar_ID_6283 Human_SNP_ID_124971997 A-to-I Human chr3 + 19954671 19954671 19954671 AAAACCCCGTCTTTACAAAAAATACGAAAATTAACCGGGCATGGTGGCACACACCTGTAGTCCCA AAAACCCCGTCTTTACAAAAAATACGAAAATTCACCGGGCATGGTGGCACACACCTGTAGTCCCA A C RAB5A Ensembl:ENSG00000144566 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs546095782 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25727265 RMVar_hsa_circ_59041,RMVar_hsa_circ_82064,RMVar_hsa_circ_216358 6284 RMVar_ID_6284 Human_SNP_ID_124972021 A-to-I Human chr3 + 19954781 19954781 19954781 CGGAGGTTACAGTGAGCCGAGACTGCACCACCACACTCCAGCCTGGGTGACAGTGAGAACCCTGT CGGAGGTTACAGTGAGCCGAGACTGCACCACCGCACTCCAGCCTGGGTGACAGTGAGAACCCTGT A G RAB5A Ensembl:ENSG00000144566 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1218573905 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25769489 RMVar_hsa_circ_59041,RMVar_hsa_circ_82064,RMVar_hsa_circ_216358 6285 RMVar_ID_6285 Human_SNP_ID_124975036 A-to-I Human chr3 + 19965299 19965299 19965299 CTAGTGTTAGCCGGGTGTGGTTGTGTGTGCCTATAGTCCCAACTACTCTGGAGGCTGACTTGGGA CTAGTGTTAGCCGGGTGTGGTTGTGTGTGCCTGTAGTCCCAACTACTCTGGAGGCTGACTTGGGA A G RAB5A Ensembl:ENSG00000144566 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs545635778 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59041,RMVar_hsa_circ_82064,RMVar_hsa_circ_216358 6286 RMVar_ID_6286 Human_SNP_ID_124978261 A-to-I Human chr3 + 19976551 19976551 19976551 CTACTAAAAATACAAAATTAGCTGGAGATGGTAGTGCATGCCTGTAATCCCAGCTACTTGGGAGG CTACTAAAAATACAAAATTAGCTGGAGATGGTGGTGCATGCCTGTAATCCCAGCTACTTGGGAGG A G RAB5A Ensembl:ENSG00000144566 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1040865173 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12430,RMVar_hsa_circ_82064,RMVar_hsa_circ_216358,RMVar_hsa_circ_279786,RMVar_hsa_circ_216361,RMVar_hsa_circ_322995,RMVar_hsa_circ_216362 6287 RMVar_ID_6287 Human_SNP_ID_124978452 A-to-I Human chr3 + 19977212 19977212 19977212 CTGCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCGCCCACCACCACTCCTGGCTAATTTTT CTGCTGCCTCAGCCTCCCAAGTAGCTGGGACTGCAGGCGCCCACCACCACTCCTGGCTAATTTTT A G RAB5A Ensembl:ENSG00000144566 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1040482889 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12430,RMVar_hsa_circ_82064,RMVar_hsa_circ_216358,RMVar_hsa_circ_279786,RMVar_hsa_circ_216361,RMVar_hsa_circ_322995,RMVar_hsa_circ_216362 6288 RMVar_ID_6288 Human_SNP_ID_124978498 A-to-I Human chr3 + 19977333 19977333 19977333 CCTGACCTTGTGATCCACCCGCCTCCGCCTCCAAAAGTGCTAGGATTACAGGCGTGAGCCACCAC CCTGACCTTGTGATCCACCCGCCTCCGCCTCCCAAAGTGCTAGGATTACAGGCGTGAGCCACCAC A C RAB5A Ensembl:ENSG00000144566 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1384232477 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12430,RMVar_hsa_circ_82064,RMVar_hsa_circ_216358,RMVar_hsa_circ_279786,RMVar_hsa_circ_216361,RMVar_hsa_circ_322995,RMVar_hsa_circ_216362 6289 RMVar_ID_6289 Human_SNP_ID_124979010 A-to-I Human chr3 + 19979046 19979046 19979046 TCGCCCAGGCTGGAGTGCAATGGTACGATCTCAGCTCACTGCAACCTCCACTTCCCGGATTCAAG TCGCCCAGGCTGGAGTGCAATGGTACGATCTCGGCTCACTGCAACCTCCACTTCCCGGATTCAAG A G RAB5A Ensembl:ENSG00000144566 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1484594733 Functional Loss SNV dbSNP153 33..33 33 - - - 6290 RMVar_ID_6290 Human_SNP_ID_124979014 A-to-I Human chr3 + 19979056 19979056 19979056 TGGAGTGCAATGGTACGATCTCAGCTCACTGCAACCTCCACTTCCCGGATTCAAGCGGTTCTCCT TGGAGTGCAATGGTACGATCTCAGCTCACTGCCACCTCCACTTCCCGGATTCAAGCGGTTCTCCT A C RAB5A Ensembl:ENSG00000144566 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1230046478 Functional Loss SNV dbSNP153 33..33 33 - - - 6291 RMVar_ID_6291 Human_SNP_ID_124979903 A-to-I Human chr3 + 19982134 19982122 19982134 TGGTGCACACCCTGTAGTCTCAGCTACTTGGAAAGCTGAGGTGGGAGGATCTTTTGAGCCCAGGA TGGTGCACACCCTGTAGTCTC____________AGCTGAGGTGGGAGGATCTTTTGAGCCCAGGA CAGCTACTTGGAA C RAB5A Ensembl:ENSG00000144566 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1295864015 Functional Loss DEL dbSNP153 22..33 33 - - - 6292 RMVar_ID_6292 Human_SNP_ID_124980207 A-to-I Human chr3 + 19983175 19983175 19983175 CCTGGGCAACATGGTGAAACCCCGTCTCTACTAAAAAACAAAAATTAGCTGGGTGTGGTGGGGCA CCTGGGCAACATGGTGAAACCCCGTCTCTACTTAAAAACAAAAATTAGCTGGGTGTGGTGGGGCA A T RAB5A Ensembl:ENSG00000144566 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1337184879 Functional Loss SNV dbSNP153 33..33 33 - - - 6293 RMVar_ID_6293 Human_SNP_ID_124980225 A-to-I Human chr3 + 19983261 19983243 19983262 GAGAGGCCAAGGCACGAGAATCACTTGAACCCAGGAGGTGGAGGTTGCAGTGAACTGAGATCACG GAGAGGCCAAGGCAC___________________GAGGTGGAGGTTGCAGTGAACTGAGATCACG CGAGAATCACTTGAACCCAG C RAB5A Ensembl:ENSG00000144566 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1269102993 Functional Loss DEL dbSNP153 16..34 33 - - - 6294 RMVar_ID_6294 Human_SNP_ID_125016694 A-to-I Human chr3 + 20121842 20121842 20121842 AATCAGTGGGTAGACTCATGAACAAGCCTGCCAAGATTGAATGAGATGAGCTGAAATCAGCCACC AATCAGTGGGTAGACTCATGAACAAGCCTGCCGAGATTGAATGAGATGAGCTGAAATCAGCCACC A G KAT2B Ensembl:ENSG00000114166 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048125916 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1643,RMVar_hsa_circ_47393,RMVar_hsa_circ_59577,RMVar_hsa_circ_264963,RMVar_hsa_circ_359691,RMVar_hsa_circ_67552,RMVar_hsa_circ_23476,RMVar_hsa_circ_216365,RMVar_hsa_circ_352543,RMVar_hsa_circ_66482,RMVar_hsa_circ_14827,RMVar_hsa_circ_327415,RMVar_hsa_circ_340396,RMVar_hsa_circ_216368,RMVar_hsa_circ_279603,RMVar_hsa_circ_333466,RMVar_hsa_circ_216369 6295 RMVar_ID_6295 Human_SNP_ID_125019271 A-to-I Human chr3 + 20131671 20131671 20131671 CTCCCTGCGTCTGCGACCTCCTGTGCTCAGGTAATCCTCCTACCTCAGCATTCTGAGTAGTTGGG CTCCCTGCGTCTGCGACCTCCTGTGCTCAGGTGATCCTCCTACCTCAGCATTCTGAGTAGTTGGG A G KAT2B Ensembl:ENSG00000114166 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs896722993 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1643,RMVar_hsa_circ_47393,RMVar_hsa_circ_59577,RMVar_hsa_circ_359691,RMVar_hsa_circ_216365,RMVar_hsa_circ_66482,RMVar_hsa_circ_12718,RMVar_hsa_circ_14827,RMVar_hsa_circ_279603,RMVar_hsa_circ_333466,RMVar_hsa_circ_216369,RMVar_hsa_circ_299696,RMVar_hsa_circ_308727,RMVar_hsa_circ_28653,RMVar_hsa_circ_216371,RMVar_hsa_circ_216372,RMVar_hsa_circ_216374,RMVar_hsa_circ_33657,RMVar_hsa_circ_356532 6296 RMVar_ID_6296 Human_SNP_ID_125028310 A-to-I Human chr3 - 20168906 20168906 20168906 TCAGCCAGGCACGAGAAACTACTAACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGCAG TCAGCCAGGCACGAGAAACTACTAACACCTGTGATCCCAGCACTTTGGGAGGCCAAGGCGGGCAG T C SGO1 Ensembl:ENSG00000129810 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs542168570 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92634,RMVar_hsa_circ_216378 6297 RMVar_ID_6297 Human_SNP_ID_125028654 A-to-I Human chr3 - 20170315 20170315 20170315 CAGCTTACCGCAACCTCCGCCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGACTCCCGAGTAGCT CAGCTTACCGCAACCTCCGCCTCCCAGGTTCAGGCGATTCTCCTGCCTCAGACTCCCGAGTAGCT T C SGO1 Ensembl:ENSG00000129810 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs942915437 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92634,RMVar_hsa_circ_216378 6298 RMVar_ID_6298 Human_SNP_ID_125030543 A-to-I Human chr3 - 20176916 20176916 20176916 GGGCTGTTTCCGTAGTTAAATTGAGTTATATAATGTGTTTTCAGGTGGAACTCTCCAACTTGATA GGGCTGTTTCCGTAGTTAAATTGAGTTATATAGTGTGTTTTCAGGTGGAACTCTCCAACTTGATA T C SGO1 Ensembl:ENSG00000129810 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1449003583 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9620,RMVar_hsa_circ_92634,RMVar_hsa_circ_216378,RMVar_hsa_circ_13095,RMVar_hsa_circ_35653,RMVar_hsa_circ_66875 6299 RMVar_ID_6299 Human_SNP_ID_125522865 A-to-I Human chr3 - 21966634 21966634 21966634 GAGATTGTAGTGAACCGAGATTGCACCACTGCACTCCAACCTGGGCTACAGAGTGTGACTGCGTC GAGATTGTAGTGAACCGAGATTGCACCACTGCGCTCCAACCTGGGCTACAGAGTGTGACTGCGTC T C ZNF385D Ensembl:ENSG00000151789 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1159148929 Functional Loss SNV dbSNP153 33..33 33 - - - 6300 RMVar_ID_6300 Human_SNP_ID_125903627 A-to-I Human chr3 + 23242039 23242039 23242039 TCAAGCTATCCTGCTGCCTCAGCCTCTCAAGTAGCTGAGACTACAGGATTGGGCTAACACACCTA TCAAGCTATCCTGCTGCCTCAGCCTCTCAAGTGGCTGAGACTACAGGATTGGGCTAACACACCTA A G UBE2E2 Ensembl:ENSG00000182247 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs962727614 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1625179,Human_RBP_ID_14773277 RMVar_hsa_circ_357623,RMVar_hsa_circ_360518,RMVar_hsa_circ_216388 6301 RMVar_ID_6301 Human_SNP_ID_125903852 A-to-I Human chr3 + 23242921 23242921 23242921 CTGCCTGGCCAACATGGTGAAACCCTGTCTCTACTAAAAACACAAAACTTAGGTGGGTGTGTTGG CTGCCTGGCCAACATGGTGAAACCCTGTCTCTGCTAAAAACACAAAACTTAGGTGGGTGTGTTGG A G UBE2E2 Ensembl:ENSG00000182247 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1038403076 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_357623,RMVar_hsa_circ_360518,RMVar_hsa_circ_216388 6302 RMVar_ID_6302 Human_SNP_ID_125903853 A-to-I Human chr3 + 23242924 23242924 23242924 CCTGGCCAACATGGTGAAACCCTGTCTCTACTAAAAACACAAAACTTAGGTGGGTGTGTTGGCTT CCTGGCCAACATGGTGAAACCCTGTCTCTACTGAAAACACAAAACTTAGGTGGGTGTGTTGGCTT A G UBE2E2 Ensembl:ENSG00000182247 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs919949097 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_357623,RMVar_hsa_circ_360518,RMVar_hsa_circ_216388 6303 RMVar_ID_6303 Human_SNP_ID_125903855 A-to-I Human chr3 + 23242927 23242927 23242927 GGCCAACATGGTGAAACCCTGTCTCTACTAAAAACACAAAACTTAGGTGGGTGTGTTGGCTTATG GGCCAACATGGTGAAACCCTGTCTCTACTAAACACACAAAACTTAGGTGGGTGTGTTGGCTTATG A C UBE2E2 Ensembl:ENSG00000182247 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs929975624 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_357623,RMVar_hsa_circ_360518,RMVar_hsa_circ_216388 6304 RMVar_ID_6304 Human_SNP_ID_125904999 A-to-I Human chr3 + 23247083 23247083 23247083 TGTTATGTTGCCCACGTTGGTCTTGAAATCCTAGACCCAAGCAGTCCTCCTGCCTCAGCTCCCAA TGTTATGTTGCCCACGTTGGTCTTGAAATCCTGGACCCAAGCAGTCCTCCTGCCTCAGCTCCCAA A G UBE2E2 Ensembl:ENSG00000182247 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1344315067 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14773418 RMVar_hsa_circ_357623,RMVar_hsa_circ_360518,RMVar_hsa_circ_216388 6305 RMVar_ID_6305 Human_SNP_ID_125905091 A-to-I Human chr3 + 23247410 23247410 23247410 CGGAGTCTCGCTCTGTCACCAGGCTGGAGTGCAATGGCATGATCTCGGCTCACCAGAACCTCTGC CGGAGTCTCGCTCTGTCACCAGGCTGGAGTGCGATGGCATGATCTCGGCTCACCAGAACCTCTGC A G UBE2E2 Ensembl:ENSG00000182247 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs552873373 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_357623,RMVar_hsa_circ_360518,RMVar_hsa_circ_216388 6306 RMVar_ID_6306 Human_SNP_ID_125905117 A-to-I Human chr3 + 23247472 23247472 23247472 TGCCTCCCGCGTACAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGTGCCCG TGCCTCCCGCGTACAAGCGATTCTCCTGCCTCGGCCTCCTGAGTAGCTGGGATTACAGGTGCCCG A G UBE2E2 Ensembl:ENSG00000182247 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs377490269 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_357623,RMVar_hsa_circ_360518,RMVar_hsa_circ_216388 6307 RMVar_ID_6307 Human_SNP_ID_125905142 A-to-I Human chr3 + 23247556 23247556 23247556 TTTGTATTTTCAGTAGGACGGGGTTTCTCCATATTGGTCAGGCTGGTCTCAAACTCTCAACCTCA TTTGTATTTTCAGTAGGACGGGGTTTCTCCATCTTGGTCAGGCTGGTCTCAAACTCTCAACCTCA A C UBE2E2 Ensembl:ENSG00000182247 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs918217156 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7180589 RMVar_hsa_circ_357623,RMVar_hsa_circ_360518,RMVar_hsa_circ_216388 6308 RMVar_ID_6308 Human_SNP_ID_125905512 A-to-I Human chr3 + 23249015 23249015 23249015 TATTCTGGCCGGGTGCAGTGGCTCATGCCTGTAATTCTAGCACTTTGAGAGGCTGACGTGGGAGG TATTCTGGCCGGGTGCAGTGGCTCATGCCTGTTATTCTAGCACTTTGAGAGGCTGACGTGGGAGG A T UBE2E2 Ensembl:ENSG00000182247 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1478033769 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14773511,Human_RBP_ID_17024588 RMVar_hsa_circ_357623,RMVar_hsa_circ_360518,RMVar_hsa_circ_216388 6309 RMVar_ID_6309 Human_SNP_ID_125907191 A-to-I Human chr3 + 23255225 23255225 23255225 CCCACATCAGCCTCCTAGGTAGATGGGACTACAGGCACACACCACTGTGCCCCGCTAATTTTTGT CCCACATCAGCCTCCTAGGTAGATGGGACTACGGGCACACACCACTGTGCCCCGCTAATTTTTGT A G UBE2E2 Ensembl:ENSG00000182247 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs563033806 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_357623,RMVar_hsa_circ_360518,RMVar_hsa_circ_216388 6310 RMVar_ID_6310 Human_SNP_ID_125907937 A-to-I Human chr3 + 23257599 23257599 23257599 TCTCATGAGGCCCAGACTGGACTCTAATTCCTAGGCACAAGTGATCCTCCCACCTCAGCCTCCGT TCTCATGAGGCCCAGACTGGACTCTAATTCCTGGGCACAAGTGATCCTCCCACCTCAGCCTCCGT A G UBE2E2 Ensembl:ENSG00000182247 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1196713548 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7180646,Human_RBP_ID_14773749 RMVar_hsa_circ_357623,RMVar_hsa_circ_360518,RMVar_hsa_circ_216388 6311 RMVar_ID_6311 Human_SNP_ID_125908907 A-to-I Human chr3 + 23260999 23260999 23260999 GTGGCATGTGCCTGTAGTCTCAGCTACCTGGGAAGCTGATGTGGGAGGATCTCTTGAGCCCAGGA GTGGCATGTGCCTGTAGTCTCAGCTACCTGGGGAGCTGATGTGGGAGGATCTCTTGAGCCCAGGA A G UBE2E2 Ensembl:ENSG00000182247 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs759999517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14773817 RMVar_hsa_circ_357623,RMVar_hsa_circ_360518 6312 RMVar_ID_6312 Human_SNP_ID_125917431 A-to-I Human chr3 + 23290387 23290387 23290387 AATGTATGTGTAAATCACCTGGAGGTCTTGTTAAAAGTGTAGACCTTGTTTTAGAGATCTGGGAT AATGTATGTGTAAATCACCTGGAGGTCTTGTTTAAAGTGTAGACCTTGTTTTAGAGATCTGGGAT A T UBE2E2 Ensembl:ENSG00000182247 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1369144031 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14774533,Human_RBP_ID_23994769 RMVar_hsa_circ_357623,RMVar_hsa_circ_360518 6313 RMVar_ID_6313 Human_SNP_ID_125917858 A-to-I Human chr3 + 23291708 23291708 23291708 TAAGGGGCTTTTTTTTTTTTTTTTTTTTTGACAGGGTCACTCTGTTGCCCAGGCTGGAGTGCAGT TAAGGGGCTTTTTTTTTTTTTTTTTTTTTGACTGGGTCACTCTGTTGCCCAGGCTGGAGTGCAGT A T UBE2E2 Ensembl:ENSG00000182247 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1327124362 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14774566 RMVar_hsa_circ_357623,RMVar_hsa_circ_360518 6314 RMVar_ID_6314 Human_SNP_ID_125922620 A-to-I Human chr3 + 23305753 23305752 23305754 ACCATTCTTTTTATTTTTTATTTTTTACAGACAGGCTCTCACTCTGTCACCCAGGTTGGAGTATA ACCATTCTTTTTATTTTTTATTTTTTACAGAC__GCTCTCACTCTGTCACCCAGGTTGGAGTATA CAG C UBE2E2 Ensembl:ENSG00000182247 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1309288159 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_7180833,Human_RBP_ID_14774777 RMVar_hsa_circ_357623,RMVar_hsa_circ_360518 6315 RMVar_ID_6315 Human_SNP_ID_125926145 A-to-I Human chr3 + 23318661 23318661 23318661 GTGAAAGGGGAAACCCCTTATAAAAACATCAGATCTGGTGAGACTTTTACTTACCACTTATTCAC GTGAAAGGGGAAACCCCTTATAAAAACATCAGCTCTGGTGAGACTTTTACTTACCACTTATTCAC A C UBE2E2 Ensembl:ENSG00000182247 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs752535526 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_357623,RMVar_hsa_circ_360518 6316 RMVar_ID_6316 Human_SNP_ID_125928886 A-to-I Human chr3 + 23329015 23329015 23329015 GGCTTTTTGCACATGCACTATTTAAATTGAGTACAATACTCAATACTTACGCCCTTGCCCCCTTC GGCTTTTTGCACATGCACTATTTAAATTGAGTGCAATACTCAATACTTACGCCCTTGCCCCCTTC A G UBE2E2 Ensembl:ENSG00000182247 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1302796990 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_357623,RMVar_hsa_circ_360518 6317 RMVar_ID_6317 Human_SNP_ID_125941613 A-to-I Human chr3 + 23371163 23371163 23371163 GTGATCCTCCCATTTCAGCATCCCAAGTAGCTAGGAGTACAGCTGCATGCCACCGCACCTGGCTA GTGATCCTCCCATTTCAGCATCCCAAGTAGCTGGGAGTACAGCTGCATGCCACCGCACCTGGCTA A G UBE2E2 Ensembl:ENSG00000182247 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs948710305 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7181071 RMVar_hsa_circ_357623,RMVar_hsa_circ_360518 6318 RMVar_ID_6318 Human_SNP_ID_125949820 A-to-I Human chr3 + 23402114 23402114 23402114 CCTGACAGGTGATCCACCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCG CCTGACAGGTGATCCACCTGCCTCAGCCTCCCGAAGTGCTGGGATTACAGGCGTGAGCCACCGCG A G UBE2E2 Ensembl:ENSG00000182247 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1344098613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25728330 RMVar_hsa_circ_357623,RMVar_hsa_circ_360518 6319 RMVar_ID_6319 Human_SNP_ID_125950161 A-to-I Human chr3 + 23403549 23403549 23403549 ATGCATTAAATGTCATTGTAGGGGCTGGGCACAGTGGCTCATGCCTGTAATCCCAGCACTTAGGG ATGCATTAAATGTCATTGTAGGGGCTGGGCACGGTGGCTCATGCCTGTAATCCCAGCACTTAGGG A G UBE2E2 Ensembl:ENSG00000182247 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1338970443 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_357623,RMVar_hsa_circ_360518 6320 RMVar_ID_6320 Human_SNP_ID_125976032 A-to-I Human chr3 + 23503644 23503644 23503644 GGGAGGCTGAGACAGGTGGATCATTTGAGATCAGGAGTTCGAGACCAGCCTGGCCAACATGGCAA GGGAGGCTGAGACAGGTGGATCATTTGAGATCCGGAGTTCGAGACCAGCCTGGCCAACATGGCAA A C UBE2E2 Ensembl:ENSG00000182247 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992946635 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_357623,RMVar_hsa_circ_216390,RMVar_hsa_circ_283041 6321 RMVar_ID_6321 Human_SNP_ID_125976056 A-to-I Human chr3 + 23503747 23503747 23503747 ATGGTGACTCACACTTGTAATTCCAGCTTCTCAGGAGGCTGAGGCATGAGAATTACTTGAACCCA ATGGTGACTCACACTTGTAATTCCAGCTTCTCGGGAGGCTGAGGCATGAGAATTACTTGAACCCA A G UBE2E2 Ensembl:ENSG00000182247 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1323538828 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_357623,RMVar_hsa_circ_216390,RMVar_hsa_circ_283041 6322 RMVar_ID_6322 Human_SNP_ID_126066252 A-to-I Human chr3 + 23846335 23846335 23846335 CTGTAGTCCTAGCTACTTGGGAGGCTTGAGGTAGGAGGATTGCTTGAGGCTAGGAGTTTGAGTTC CTGTAGTCCTAGCTACTTGGGAGGCTTGAGGTGGGAGGATTGCTTGAGGCTAGGAGTTTGAGTTC A G UBE2E1 Ensembl:ENSG00000170142 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs940534995 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7182087 RMVar_hsa_circ_358580 6323 RMVar_ID_6323 Human_SNP_ID_126066325 A-to-I Human chr3 + 23846621 23846621 23846621 GGGAGGCTGAGGCCCGGCAATCACTTGAACCCAGGGGGCGGAGGCTGCAGTGAGCTGAGATCGTG GGGAGGCTGAGGCCCGGCAATCACTTGAACCCCGGGGGCGGAGGCTGCAGTGAGCTGAGATCGTG A C UBE2E1 Ensembl:ENSG00000170142 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1429594703 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_358580 6324 RMVar_ID_6324 Human_SNP_ID_126066793 A-to-I Human chr3 + 23848259 23848259 23848259 GGGAGGCCAAGGCGGATGGATCACTTGAGGTCAGGAGTTTGAGACCAGCCTGGCCAACATGATGA GGGAGGCCAAGGCGGATGGATCACTTGAGGTCGGGAGTTTGAGACCAGCCTGGCCAACATGATGA A G UBE2E1 Ensembl:ENSG00000170142 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs780917494 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_358580 6325 RMVar_ID_6325 Human_SNP_ID_126081557 A-to-I Human chr3 + 23901374 23901373 23901375 GCCCAGTGAATTCTTGTACTTTTTGTAGAGACAGGGTTTCACCACGTGGCCCAGGCTGGTCTCGA GCCCAGTGAATTCTTGTACTTTTTGTAGAGAC__GGTTTCACCACGTGGCCCAGGCTGGTCTCGA CAG C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1491491916 Functional Loss DEL dbSNP153 33..34 33 - - - 6326 RMVar_ID_6326 Human_SNP_ID_126082052 A-to-I Human chr3 + 23903383 23903383 23903383 GCAATCTGCCTGCTTCTGCCTCCCAAAGTGCTAGGATTACAGGCATGAGCCACTGCACTGGGCCT GCAATCTGCCTGCTTCTGCCTCCCAAAGTGCTCGGATTACAGGCATGAGCCACTGCACTGGGCCT A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1435319226 Functional Loss SNV dbSNP153 33..33 33 - - - 6327 RMVar_ID_6327 Human_SNP_ID_126087696 A-to-I Human chr3 + 23921714 23921714 23921714 CTTCTGCCTCGGCCTCCCAAATAGCCAGGACTACAGGCGCACACTGCCATGCCCAGCTAAGTTTT CTTCTGCCTCGGCCTCCCAAATAGCCAGGACTGCAGGCGCACACTGCCATGCCCAGCTAAGTTTT A G RPL15 Ensembl:ENSG00000174748 Protein coding 3'UTR GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs762026925 Functional Loss SNV dbSNP153 33..33 33 - - - 6328 RMVar_ID_6328 Human_SNP_ID_126087745 A-to-I Human chr3 + 23921894 23921894 23921894 ACCACCCCCAGCCCAATTTTTATTTTTTGTACAGACAGGATCTCACTATGTTGCCCAGGTTGGTC ACCACCCCCAGCCCAATTTTTATTTTTTGTACCGACAGGATCTCACTATGTTGCCCAGGTTGGTC A C RPL15 Ensembl:ENSG00000174748 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935504610 Functional Loss SNV dbSNP153 33..33 33 - - - 6329 RMVar_ID_6329 Human_SNP_ID_126096810 A-to-I Human chr3 + 23953287 23953287 23953287 ATTGCTTGGACCCAGGAGGTGGAGGTTGCTGTAAGTCGAGATTGTGACACTGCACTCCGGCCTGG ATTGCTTGGACCCAGGAGGTGGAGGTTGCTGTGAGTCGAGATTGTGACACTGCACTCCGGCCTGG A G NR1D2 Ensembl:ENSG00000174738 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459663293 Functional Loss SNV dbSNP153 33..33 33 - - - 6330 RMVar_ID_6330 Human_SNP_ID_126097112 A-to-I Human chr3 + 23954276 23954276 23954276 AGCGACAATCCTCCCACCTCAGCCCCCAAAGTACTATGATTACAGGCATGAGCCAGTGTGCCGGG AGCGACAATCCTCCCACCTCAGCCCCCAAAGTGCTATGATTACAGGCATGAGCCAGTGTGCCGGG A G NR1D2 Ensembl:ENSG00000174738 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1279732150 Functional Loss SNV dbSNP153 33..33 33 - - - 6331 RMVar_ID_6331 Human_SNP_ID_126101621 A-to-I Human chr3 + 23969258 23969258 23969258 CCGTGAGCCGAGATCACACCAGCTTGCATTCCAGCTTGGGTGACAGAGCGAGACTCCGTGTTAAA CCGTGAGCCGAGATCACACCAGCTTGCATTCCCGCTTGGGTGACAGAGCGAGACTCCGTGTTAAA A C NR1D2 Ensembl:ENSG00000174738 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270157572 Functional Loss SNV dbSNP153 33..33 33 - - - 6332 RMVar_ID_6332 Human_SNP_ID_126102035 A-to-I Human chr3 + 23970843 23970843 23970843 CTCTCTTGCTGCCCAGGCTGGAGTGCAATGGCATGATCTCTGTTCACCGCAACCTCCCTCTCCTA CTCTCTTGCTGCCCAGGCTGGAGTGCAATGGCGTGATCTCTGTTCACCGCAACCTCCCTCTCCTA A G NR1D2 Ensembl:ENSG00000174738 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910051966 Functional Loss SNV dbSNP153 33..33 33 - - - 6333 RMVar_ID_6333 Human_SNP_ID_126231049 A-to-I Human chr3 - 24473936 24473936 24473936 TTCATCCCCCAACACCCAACAGGCCACAGTGTATGATGTTCCCCTCCCTGTGTCCATGTGTTCTC TTCATCCCCCAACACCCAACAGGCCACAGTGTGTGATGTTCCCCTCCCTGTGTCCATGTGTTCTC T C THRB Ensembl:ENSG00000151090 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1336118304 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17089135 6334 RMVar_ID_6334 Human_SNP_ID_126561569 A-to-I Human chr3 - 25621427 25621427 25621427 AGCCCAGGTGGTTGAGGCTGCAGTGAGCTGATATCGTGCCACGGCACTCCAGCCTGGGTGACAAA AGCCCAGGTGGTTGAGGCTGCAGTGAGCTGATGTCGTGCCACGGCACTCCAGCCTGGGTGACAAA T C TOP2B Ensembl:ENSG00000077097 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1392786703 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25730018 RMVar_hsa_circ_2809,RMVar_hsa_circ_4992,RMVar_hsa_circ_86264,RMVar_hsa_circ_121985,RMVar_hsa_circ_116280,RMVar_hsa_circ_109342,RMVar_hsa_circ_92319,RMVar_hsa_circ_216436,RMVar_hsa_circ_216438,RMVar_hsa_circ_216440,RMVar_hsa_circ_78593,RMVar_hsa_circ_216439,RMVar_hsa_circ_216437,RMVar_hsa_circ_216435,RMVar_hsa_circ_299340,RMVar_hsa_circ_32892,RMVar_hsa_circ_216443,RMVar_hsa_circ_41683,RMVar_hsa_circ_74197,RMVar_hsa_circ_62915,RMVar_hsa_circ_37506,RMVar_hsa_circ_40884,RMVar_hsa_circ_7607,RMVar_hsa_circ_216448,RMVar_hsa_circ_70993,RMVar_hsa_circ_321189,RMVar_hsa_circ_216449,RMVar_hsa_circ_74828,RMVar_hsa_circ_60084,RMVar_hsa_circ_350032,RMVar_hsa_circ_81240,RMVar_hsa_circ_12987,RMVar_hsa_circ_376791,RMVar_hsa_circ_40037,RMVar_hsa_circ_100560,RMVar_hsa_circ_117243,RMVar_hsa_circ_216456,RMVar_hsa_circ_108180,RMVar_hsa_circ_85158,RMVar_hsa_circ_216458,RMVar_hsa_circ_216460,RMVar_hsa_circ_71960,RMVar_hsa_circ_216461,RMVar_hsa_circ_216459,RMVar_hsa_circ_216457 6335 RMVar_ID_6335 Human_SNP_ID_126561599 A-to-I Human chr3 - 25621557 25621557 25621557 CAGGAGTTGAAGACCAGCCTGGGCAACATGGCAAAACCCTGTCTCTACAAAAATACAAAAATTAG CAGGAGTTGAAGACCAGCCTGGGCAACATGGCGAAACCCTGTCTCTACAAAAATACAAAAATTAG T C TOP2B Ensembl:ENSG00000077097 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1368672745 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2809,RMVar_hsa_circ_4992,RMVar_hsa_circ_86264,RMVar_hsa_circ_121985,RMVar_hsa_circ_116280,RMVar_hsa_circ_109342,RMVar_hsa_circ_92319,RMVar_hsa_circ_216436,RMVar_hsa_circ_216438,RMVar_hsa_circ_216440,RMVar_hsa_circ_78593,RMVar_hsa_circ_216439,RMVar_hsa_circ_216437,RMVar_hsa_circ_216435,RMVar_hsa_circ_299340,RMVar_hsa_circ_32892,RMVar_hsa_circ_216443,RMVar_hsa_circ_41683,RMVar_hsa_circ_74197,RMVar_hsa_circ_62915,RMVar_hsa_circ_37506,RMVar_hsa_circ_40884,RMVar_hsa_circ_7607,RMVar_hsa_circ_216448,RMVar_hsa_circ_70993,RMVar_hsa_circ_321189,RMVar_hsa_circ_216449,RMVar_hsa_circ_74828,RMVar_hsa_circ_60084,RMVar_hsa_circ_350032,RMVar_hsa_circ_81240,RMVar_hsa_circ_12987,RMVar_hsa_circ_376791,RMVar_hsa_circ_40037,RMVar_hsa_circ_100560,RMVar_hsa_circ_117243,RMVar_hsa_circ_216456,RMVar_hsa_circ_108180,RMVar_hsa_circ_85158,RMVar_hsa_circ_216458,RMVar_hsa_circ_216460,RMVar_hsa_circ_71960,RMVar_hsa_circ_216461,RMVar_hsa_circ_216459,RMVar_hsa_circ_216457 6336 RMVar_ID_6336 Human_SNP_ID_126561614 A-to-I Human chr3 - 25621634 25621634 25621634 TTAGAGTAGGCCAGGTGCAGTGACTCATGTCTATAATCCCAGCACTTTGGGAGGCTGAGCTGGGC TTAGAGTAGGCCAGGTGCAGTGACTCATGTCTCTAATCCCAGCACTTTGGGAGGCTGAGCTGGGC T G TOP2B Ensembl:ENSG00000077097 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1207234259 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2809,RMVar_hsa_circ_4992,RMVar_hsa_circ_86264,RMVar_hsa_circ_121985,RMVar_hsa_circ_116280,RMVar_hsa_circ_109342,RMVar_hsa_circ_92319,RMVar_hsa_circ_216436,RMVar_hsa_circ_216438,RMVar_hsa_circ_216440,RMVar_hsa_circ_78593,RMVar_hsa_circ_216439,RMVar_hsa_circ_216437,RMVar_hsa_circ_216435,RMVar_hsa_circ_299340,RMVar_hsa_circ_32892,RMVar_hsa_circ_216443,RMVar_hsa_circ_41683,RMVar_hsa_circ_74197,RMVar_hsa_circ_62915,RMVar_hsa_circ_37506,RMVar_hsa_circ_40884,RMVar_hsa_circ_7607,RMVar_hsa_circ_216448,RMVar_hsa_circ_70993,RMVar_hsa_circ_321189,RMVar_hsa_circ_216449,RMVar_hsa_circ_74828,RMVar_hsa_circ_60084,RMVar_hsa_circ_350032,RMVar_hsa_circ_81240,RMVar_hsa_circ_12987,RMVar_hsa_circ_376791,RMVar_hsa_circ_40037,RMVar_hsa_circ_100560,RMVar_hsa_circ_117243,RMVar_hsa_circ_216456,RMVar_hsa_circ_108180,RMVar_hsa_circ_85158,RMVar_hsa_circ_216458,RMVar_hsa_circ_216460,RMVar_hsa_circ_71960,RMVar_hsa_circ_216461,RMVar_hsa_circ_216459,RMVar_hsa_circ_216457 6337 RMVar_ID_6337 Human_SNP_ID_126569377 A-to-I Human chr3 - 25651802 25651802 25651802 GAAGTACAGTGGCACAATCTTGGCTCACTGCAACCTCTGCCTCAGGTTCAAGTGATTCTTCTGCC GAAGTACAGTGGCACAATCTTGGCTCACTGCAGCCTCTGCCTCAGGTTCAAGTGATTCTTCTGCC T C TOP2B Ensembl:ENSG00000077097 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1209664414 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78593,RMVar_hsa_circ_216435,RMVar_hsa_circ_216477 6338 RMVar_ID_6338 Human_SNP_ID_127030069 A-to-I Human chr3 - 27373404 27373404 27373404 ATATGTGAAATGTCTTTTGGTTTATTCCAACAATTATTTATTTTAGAAAGTAAGTTTAAAGACTT ATATGTGAAATGTCTTTTGGTTTATTCCAACAGTTATTTATTTTAGAAAGTAAGTTTAAAGACTT T C SLC4A7 Ensembl:ENSG00000033867 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs187211286 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_599524,Human_RBP_ID_2778499,Human_RBP_ID_7184548,Human_RBP_ID_17703775,Human_RBP_ID_23288356,Human_RBP_ID_27717611 Human_miRNA_ID_1775062 6339 RMVar_ID_6339 Human_SNP_ID_127032179 A-to-I Human chr3 - 27382205 27382205 27382205 TGAGGCAGGACAGTTGGTTGAACCCAGGAGGCAGAGATTGCAGTGAGCCAAGATCATACCAGTGC TGAGGCAGGACAGTTGGTTGAACCCAGGAGGCGGAGATTGCAGTGAGCCAAGATCATACCAGTGC T C SLC4A7 Ensembl:ENSG00000033867 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1166377141 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17573534 RMVar_hsa_circ_216512,RMVar_hsa_circ_41208,RMVar_hsa_circ_216510,RMVar_hsa_circ_216511,RMVar_hsa_circ_284163,RMVar_hsa_circ_290390,RMVar_hsa_circ_324409,RMVar_hsa_circ_325668,RMVar_hsa_circ_306024,RMVar_hsa_circ_286857,RMVar_hsa_circ_275807,RMVar_hsa_circ_282283,RMVar_hsa_circ_271091,RMVar_hsa_circ_216516,RMVar_hsa_circ_216520,RMVar_hsa_circ_9998,RMVar_hsa_circ_15937,RMVar_hsa_circ_216522,RMVar_hsa_circ_216523,RMVar_hsa_circ_216521,RMVar_hsa_circ_216518,RMVar_hsa_circ_216519,RMVar_hsa_circ_216517,RMVar_hsa_circ_216514,RMVar_hsa_circ_216515,RMVar_hsa_circ_216513 6340 RMVar_ID_6340 Human_SNP_ID_127051035 A-to-I Human chr3 - 27455850 27455850 27455850 AGGTTTTGTTTTTTGTGTTTTTTTTTGAGACAAGGTCTCGTTCTGTTGCCCAGGCTAGAGTGCGG AGGTTTTGTTTTTTGTGTTTTTTTTTGAGACAGGGTCTCGTTCTGTTGCCCAGGCTAGAGTGCGG T C SLC4A7 Ensembl:ENSG00000033867 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991517853 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3704375,Human_RBP_ID_14784279 RMVar_hsa_circ_100194,RMVar_hsa_circ_216560 6341 RMVar_ID_6341 Human_SNP_ID_127055350 A-to-I Human chr3 - 27471575 27471575 27471575 CTGAGGTCAGGAGTTTGAGACCAGTCTGACCAACGTGGAGGAACCCCATCTCTACTAAAAATACA CTGAGGTCAGGAGTTTGAGACCAGTCTGACCACCGTGGAGGAACCCCATCTCTACTAAAAATACA T G SLC4A7 Ensembl:ENSG00000033867 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1203871795 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14784529 RMVar_hsa_circ_100194,RMVar_hsa_circ_216560 6342 RMVar_ID_6342 Human_SNP_ID_127056143 A-to-I Human chr3 - 27474527 27474527 27474527 TTTTGTATTTTTAGTAGGGACCGGGTTTCACTATGTTGGCCAGACTGGTCTCAAACTCCTGACCT TTTTGTATTTTTAGTAGGGACCGGGTTTCACTGTGTTGGCCAGACTGGTCTCAAACTCCTGACCT T C SLC4A7 Ensembl:ENSG00000033867 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs999477153 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100194,RMVar_hsa_circ_216560 6343 RMVar_ID_6343 Human_SNP_ID_127056233 A-to-I Human chr3 - 27474925 27474925 27474925 TTTTGTGTTTGTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCAGGTCTCGAACTCCTGACCT TTTTGTGTTTGTAGTAGAGATGGGGTTTCACCCTGTTGGCCAGGCAGGTCTCGAACTCCTGACCT T G SLC4A7 Ensembl:ENSG00000033867 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1421762398 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100194,RMVar_hsa_circ_216560 6344 RMVar_ID_6344 Human_SNP_ID_127059532 A-to-I Human chr3 - 27486518 27486518 27486518 CAAGCATAGCACTTGCGGCAGATCATCTTGTCACAGTTGTATTTCTGGGAGAGCTGGCAGAGGGA CAAGCATAGCACTTGCGGCAGATCATCTTGTCGCAGTTGTATTTCTGGGAGAGCTGGCAGAGGGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878981397 Functional Loss SNV dbSNP153 33..33 33 - - - 6345 RMVar_ID_6345 Human_SNP_ID_127059539 A-to-I Human chr3 - 27486549 27486549 27486549 CTTGCAGCAGTTGACAGCACGGGGGTGCAGGCAAGCATAGCACTTGCGGCAGATCATCTTGTCAC CTTGCAGCAGTTGACAGCACGGGGGTGCAGGCGAGCATAGCACTTGCGGCAGATCATCTTGTCAC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878860848 Functional Loss SNV dbSNP153 33..33 33 - - - 6346 RMVar_ID_6346 Human_SNP_ID_127245797 A-to-I Human chr3 - 28220877 28220877 28220877 TAGGATGTTGTGATATATGAAGCAAGACAGGTATTGCCCAGACTGGGGCAGGCCAGTGAGGATGA TAGGATGTTGTGATATATGAAGCAAGACAGGTGTTGCCCAGACTGGGGCAGGCCAGTGAGGATGA T C HSALNG0024841 RNACentral:URS0000EB038B lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1189421308 Functional Loss SNV dbSNP153 33..33 33 - - - 6347 RMVar_ID_6347 Human_SNP_ID_127251119 A-to-I Human chr3 + 28243130 28243130 28243130 CAGGCTGGAGTGCAGTGGCGCTATCTCGGCTCACTGTAGCCTCCGCCTACTGGGTTCAAGCAATT CAGGCTGGAGTGCAGTGGCGCTATCTCGGCTCCCTGTAGCCTCCGCCTACTGGGTTCAAGCAATT A C CMC1 Ensembl:ENSG00000187118 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs977880843 Functional Loss SNV dbSNP153 33..33 33 - - - 6348 RMVar_ID_6348 Human_SNP_ID_127251153 A-to-I Human chr3 + 28243230 28243230 28243230 GGCGCCCGCCACCACGGCCGGCTAATTTTTGTATTTTTAGTAGAGATGAGGTTTCGCCGTGTTCG GGCGCCCGCCACCACGGCCGGCTAATTTTTGTGTTTTTAGTAGAGATGAGGTTTCGCCGTGTTCG A G CMC1 Ensembl:ENSG00000187118 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1241697523 Functional Loss SNV dbSNP153 33..33 33 - - - 6349 RMVar_ID_6349 Human_SNP_ID_127251154 A-to-I Human chr3 + 28243236 28243236 28243236 CGCCACCACGGCCGGCTAATTTTTGTATTTTTAGTAGAGATGAGGTTTCGCCGTGTTCGCCATGC CGCCACCACGGCCGGCTAATTTTTGTATTTTTGGTAGAGATGAGGTTTCGCCGTGTTCGCCATGC A G CMC1 Ensembl:ENSG00000187118 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs761862955 Functional Loss SNV dbSNP153 33..33 33 - - - 6350 RMVar_ID_6350 Human_SNP_ID_127251171 A-to-I Human chr3 + 28243290 28243290 28243290 GTTCGCCATGCTGGTCTGGAACTCCTGACCTCAAGTGATCTGCCTGACTTGGCCTCCCAAAGTGC GTTCGCCATGCTGGTCTGGAACTCCTGACCTCCAGTGATCTGCCTGACTTGGCCTCCCAAAGTGC A C CMC1 Ensembl:ENSG00000187118 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs568384390 Functional Loss SNV dbSNP153 33..33 33 - - - 6351 RMVar_ID_6351 Human_SNP_ID_127251514 A-to-I Human chr3 + 28244658 28244658 28244658 GGCTGAGGAATGAGAATTTGAGCCTGGAAGGCAGCGGTTGCAGTGAGCCGAGGTTGCGCCACTGC GGCTGAGGAATGAGAATTTGAGCCTGGAAGGCCGCGGTTGCAGTGAGCCGAGGTTGCGCCACTGC A C CMC1 Ensembl:ENSG00000187118 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs766631906 Functional Loss SNV dbSNP153 33..33 33 - - - 6352 RMVar_ID_6352 Human_SNP_ID_127272614 A-to-I Human chr3 - 28331916 28331916 28331916 TATCTGTAGCACAGCCTGGAGTGCAGTGGCGCAATCATGGGATAGCATGAATTTTGAGGACTGTT TATCTGTAGCACAGCCTGGAGTGCAGTGGCGCTATCATGGGATAGCATGAATTTTGAGGACTGTT T A AZI2 Ensembl:ENSG00000163512 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232882104 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7185265,Human_RBP_ID_10092687,Human_RBP_ID_14785830 Human_Splice_Rec_404606,Human_Splice_Rec_404610,Human_Splice_Rec_404612,Human_Splice_Rec_404624,Human_Splice_Rec_404638 RMVar_hsa_circ_87680,RMVar_hsa_circ_61704,RMVar_hsa_circ_216568 6353 RMVar_ID_6353 Human_SNP_ID_127272615 A-to-I Human chr3 - 28331916 28331916 28331916 TATCTGTAGCACAGCCTGGAGTGCAGTGGCGCAATCATGGGATAGCATGAATTTTGAGGACTGTT TATCTGTAGCACAGCCTGGAGTGCAGTGGCGCCATCATGGGATAGCATGAATTTTGAGGACTGTT T G AZI2 Ensembl:ENSG00000163512 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232882104 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7185265,Human_RBP_ID_10092687,Human_RBP_ID_14785830 Human_Splice_Rec_404606,Human_Splice_Rec_404610,Human_Splice_Rec_404612,Human_Splice_Rec_404624,Human_Splice_Rec_404638 RMVar_hsa_circ_87680,RMVar_hsa_circ_61704,RMVar_hsa_circ_216568 6354 RMVar_ID_6354 Human_SNP_ID_127273072 A-to-I Human chr3 - 28333961 28333961 28333961 GACTCTAGGGCCAAAGAAGTAAAAGAGATACTAGATCAGTAAAATTAAGTTGGTTTAGAAGACGT GACTCTAGGGCCAAAGAAGTAAAAGAGATACTGGATCAGTAAAATTAAGTTGGTTTAGAAGACGT T C AZI2 Ensembl:ENSG00000163512 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1184703460 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87680,RMVar_hsa_circ_61704,RMVar_hsa_circ_3188,RMVar_hsa_circ_39741,RMVar_hsa_circ_216568 6355 RMVar_ID_6355 Human_SNP_ID_127273077 A-to-I Human chr3 - 28333987 28333987 28333987 GAACCATTGATCCTGTGAGAAATACAGACTCTAGGGCCAAAGAAGTAAAAGAGATACTAGATCAG GAACCATTGATCCTGTGAGAAATACAGACTCTTGGGCCAAAGAAGTAAAAGAGATACTAGATCAG T A AZI2 Ensembl:ENSG00000163512 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1442790102 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87680,RMVar_hsa_circ_61704,RMVar_hsa_circ_3188,RMVar_hsa_circ_39741,RMVar_hsa_circ_216568 6356 RMVar_ID_6356 Human_SNP_ID_127273287 A-to-I Human chr3 - 28334974 28334974 28334974 GTATTTCTCACAGGATCAACTGTTCTGAATATAAATGGCTGGAATATTAGGGGACACAGTTTTAT GTATTTCTCACAGGATCAACTGTTCTGAATATGAATGGCTGGAATATTAGGGGACACAGTTTTAT T C AZI2 Ensembl:ENSG00000163512 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs901624018 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87680,RMVar_hsa_circ_61704,RMVar_hsa_circ_3188,RMVar_hsa_circ_39741,RMVar_hsa_circ_216568 6357 RMVar_ID_6357 Human_SNP_ID_127273288 A-to-I Human chr3 - 28334976 28334976 28334976 CTGTATTTCTCACAGGATCAACTGTTCTGAATATAAATGGCTGGAATATTAGGGGACACAGTTTT CTGTATTTCTCACAGGATCAACTGTTCTGAATGTAAATGGCTGGAATATTAGGGGACACAGTTTT T C AZI2 Ensembl:ENSG00000163512 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs997206894 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87680,RMVar_hsa_circ_61704,RMVar_hsa_circ_3188,RMVar_hsa_circ_39741,RMVar_hsa_circ_216568 6358 RMVar_ID_6358 Human_SNP_ID_127273294 A-to-I Human chr3 - 28335013 28335013 28335013 TGATCCAGTATCTCTTTTACTTCTTTGGCCCAAGAGTCTGTATTTCTCACAGGATCAACTGTTCT TGATCCAGTATCTCTTTTACTTCTTTGGCCCATGAGTCTGTATTTCTCACAGGATCAACTGTTCT T A AZI2 Ensembl:ENSG00000163512 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs915631975 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87680,RMVar_hsa_circ_61704,RMVar_hsa_circ_3188,RMVar_hsa_circ_39741,RMVar_hsa_circ_216568 6359 RMVar_ID_6359 Human_SNP_ID_104470522 A-to-I Human chr2 + 181928751 181928751 181928751 GGGTTCACGCCATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCGCCAGCCACTACG GGGTTCACGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCAGCCACTACG A G ITPRID2 Ensembl:ENSG00000138434 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs899663769 Functional Loss SNV dbSNP153 33..33 33 - - - 6360 RMVar_ID_6360 Human_SNP_ID_104521193 A-to-I Human chr2 - 182145536 182145536 182145536 TTTAGTAGAGACAGGGTTTCAGCGTGTTGCCCAGGCTGGTCTCGAACTCCTGAGCTCAGGCAATC TTTAGTAGAGACAGGGTTTCAGCGTGTTGCCCCGGCTGGTCTCGAACTCCTGAGCTCAGGCAATC T G PDE1A Ensembl:ENSG00000115252 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1321457313 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_204977 6361 RMVar_ID_6361 Human_SNP_ID_104577330 A-to-I Human chr2 - 182377517 182377517 182377517 TTTCTTGTCAACACTTGACAATGTCTGTATTAATCTGTTCTTGCATCACTATCAAGAAATACCTG TTTCTTGTCAACACTTGACAATGTCTGTATTATTCTGTTCTTGCATCACTATCAAGAAATACCTG T A PDE1A Ensembl:ENSG00000115252 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1481217668 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8506574 RMVar_hsa_circ_267333 6362 RMVar_ID_6362 Human_SNP_ID_104578409 A-to-I Human chr2 - 182381620 182381620 182381620 TTTATTAGAGATGGAGTTTCACCCTGTTGGCCAGGCTGGTCTCAAACTCCTGATCTCGTGATCTG TTTATTAGAGATGGAGTTTCACCCTGTTGGCCGGGCTGGTCTCAAACTCCTGATCTCGTGATCTG T C PDE1A Ensembl:ENSG00000115252 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1362907528 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267333 6363 RMVar_ID_6363 Human_SNP_ID_104600532 A-to-I Human chr2 - 182472347 182472347 182472347 TGTGGCTGAATAGTATTTCATTGTGTATATATACCACATTTTCTTTATCCAGTTATCCATTGATG TGTGGCTGAATAGTATTTCATTGTGTATATATGCCACATTTTCTTTATCCAGTTATCCATTGATG T C PDE1A Ensembl:ENSG00000115252 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs927141046 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267333 6364 RMVar_ID_6364 Human_SNP_ID_104663000 A-to-I Human chr2 + 182722677 182722677 182722677 AAACTAAAATACAGCCAGGCGCGGTGGCTCACACCTGTATAATCCCAGCACTTTGGGAGGCCAAG AAACTAAAATACAGCCAGGCGCGGTGGCTCACGCCTGTATAATCCCAGCACTTTGGGAGGCCAAG A G DNAJC10 Ensembl:ENSG00000077232 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1366578163 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2882,RMVar_hsa_circ_87514,RMVar_hsa_circ_339650,RMVar_hsa_circ_350311,RMVar_hsa_circ_204989,RMVar_hsa_circ_362787,RMVar_hsa_circ_342114,RMVar_hsa_circ_56057,RMVar_hsa_circ_40015,RMVar_hsa_circ_1840,RMVar_hsa_circ_204990,RMVar_hsa_circ_204992,RMVar_hsa_circ_204993,RMVar_hsa_circ_204991,RMVar_hsa_circ_65749 6365 RMVar_ID_6365 Human_SNP_ID_104713808 A-to-I Human chr2 - 182923559 182923547 182923560 ATAACTAATTTAACAATTTCATGGCCAGGCGTAGTGGCACACGCCTATTTCAGCACTTTGGGAGG ATAACTAATTTAACAATTTCATGGCCAGGCG_____________CTATTTCAGCACTTTGGGAGG GGCGTGTGCCACTA G NCKAP1 Ensembl:ENSG00000061676 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167201835 Functional Loss DEL dbSNP153 32..44 33 - - - 6366 RMVar_ID_6366 Human_SNP_ID_104713811 A-to-I Human chr2 - 182923559 182923559 182923559 ATAACTAATTTAACAATTTCATGGCCAGGCGTAGTGGCACACGCCTATTTCAGCACTTTGGGAGG ATAACTAATTTAACAATTTCATGGCCAGGCGTGGTGGCACACGCCTATTTCAGCACTTTGGGAGG T C NCKAP1 Ensembl:ENSG00000061676 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs927998586 Functional Loss SNV dbSNP153 33..33 33 - - - 6367 RMVar_ID_6367 Human_SNP_ID_104720254 A-to-I Human chr2 - 182950961 182950961 182950961 GGGTGTGGTGGTGGGCACTTGTAATCCCAGCTACTAGGGAGGCTGAGGCAGGAGAATCACTTGAA GGGTGTGGTGGTGGGCACTTGTAATCCCAGCTGCTAGGGAGGCTGAGGCAGGAGAATCACTTGAA T C NCKAP1 Ensembl:ENSG00000061676 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs970571476 Functional Loss SNV dbSNP153 33..33 33 - - - 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_308488,RMVar_hsa_circ_61751,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_19205,RMVar_hsa_circ_299114,RMVar_hsa_circ_205005,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_275980,RMVar_hsa_circ_290492,RMVar_hsa_circ_97135,RMVar_hsa_circ_35298,RMVar_hsa_circ_63256,RMVar_hsa_circ_26770,RMVar_hsa_circ_205013,RMVar_hsa_circ_205015,RMVar_hsa_circ_205017,RMVar_hsa_circ_205018,RMVar_hsa_circ_205019,RMVar_hsa_circ_205016,RMVar_hsa_circ_205014,RMVar_hsa_circ_205011,RMVar_hsa_circ_205012 6368 RMVar_ID_6368 Human_SNP_ID_104756546 A-to-I Human chr2 + 183096510 183096510 183096510 CACCCACCTTGGCCTCTCTAAATACTGGGATTACAGGCGTGAGCCACTGCATCCGACCTCATTTT CACCCACCTTGGCCTCTCTAAATACTGGGATTGCAGGCGTGAGCCACTGCATCCGACCTCATTTT A G DUSP19 Ensembl:ENSG00000162999 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1396719096 Functional Loss SNV dbSNP153 33..33 33 - - - 6369 RMVar_ID_6369 Human_SNP_ID_104756751 A-to-I Human chr2 + 183097296 183097296 183097296 AGTGATCCTCCCGCCTTAGCCTCCCAAGTGCTAGGATTACAGGCATCAGCCACCACGCCTGGCCT AGTGATCCTCCCGCCTTAGCCTCCCAAGTGCTGGGATTACAGGCATCAGCCACCACGCCTGGCCT A G DUSP19 Ensembl:ENSG00000162999 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs942489603 Functional Loss SNV dbSNP153 33..33 33 - - - 6370 RMVar_ID_6370 Human_SNP_ID_104756881 A-to-I Human chr2 + 183097985 183097985 183097985 GTGATCTTGGCTCACTGCAACCTCTGCCTCCCAGCTTCAAGCGATTCTCCTGTATCAGCCTCCCA GTGATCTTGGCTCACTGCAACCTCTGCCTCCCGGCTTCAAGCGATTCTCCTGTATCAGCCTCCCA A G DUSP19 Ensembl:ENSG00000162999 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1215523293 Functional Loss SNV dbSNP153 33..33 33 - - - 6371 RMVar_ID_6371 Human_SNP_ID_104756928 A-to-I Human chr2 + 183098169 183098169 183098169 CACACGCCTTGGTCTCCCAAAGTGCTGGGATTACGGTGTTAGCCACTACACCTGGCCTGGATTGT CACACGCCTTGGTCTCCCAAAGTGCTGGGATTGCGGTGTTAGCCACTACACCTGGCCTGGATTGT A G DUSP19 Ensembl:ENSG00000162999 Protein coding 3'UTR GSE47997;GSE100210;GSE107867 K562 cells&HepG2 cells;HepG2 cell line;ASD brains,temporal_cortex - 23474544,29129909,30559470 RNA-Seq:(High) rs1021980218 Functional Loss SNV dbSNP153 33..33 33 - - - 6372 RMVar_ID_6372 Human_SNP_ID_104765479 A-to-I Human chr2 + 183132162 183132162 183132162 CCTCCCACCTCTTCTCCCTAGTAGCAGGGACTACAGATGTGGACCACCATGCCTGGCTAACTTTT CCTCCCACCTCTTCTCCCTAGTAGCAGGGACTGCAGATGTGGACCACCATGCCTGGCTAACTTTT A G NUP35 Ensembl:ENSG00000163002 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1329603195 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110351,RMVar_hsa_circ_114739,RMVar_hsa_circ_205072,RMVar_hsa_circ_273283,RMVar_hsa_circ_205073,RMVar_hsa_circ_342910,RMVar_hsa_circ_115576,RMVar_hsa_circ_205076,RMVar_hsa_circ_103366,RMVar_hsa_circ_205077,RMVar_hsa_circ_205078 6373 RMVar_ID_6373 Human_SNP_ID_104765579 A-to-I Human chr2 + 183132497 183132497 183132497 GGACGATTGCTTGAGCCTGGGAAGCTCAGGCTACAGTGGGCTGTGATCGTGTTACTGCACTCAGC GGACGATTGCTTGAGCCTGGGAAGCTCAGGCTGCAGTGGGCTGTGATCGTGTTACTGCACTCAGC A G NUP35 Ensembl:ENSG00000163002 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270093063 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110351,RMVar_hsa_circ_114739,RMVar_hsa_circ_205072,RMVar_hsa_circ_273283,RMVar_hsa_circ_205073,RMVar_hsa_circ_342910,RMVar_hsa_circ_115576,RMVar_hsa_circ_205076,RMVar_hsa_circ_103366,RMVar_hsa_circ_205077,RMVar_hsa_circ_205078 6374 RMVar_ID_6374 Human_SNP_ID_104769214 A-to-I Human chr2 + 183145948 183145948 183145948 AAAAGAAAAAATATAATCACTTAAGAATTTCAAAAATCTGCTGTGCATGGTAGCTCACGCTTGGA AAAAGAAAAAATATAATCACTTAAGAATTTCAGAAATCTGCTGTGCATGGTAGCTCACGCTTGGA A G NUP35 Ensembl:ENSG00000163002 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs918494022 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13709510 RMVar_hsa_circ_114739,RMVar_hsa_circ_205073,RMVar_hsa_circ_342910,RMVar_hsa_circ_60476,RMVar_hsa_circ_103366,RMVar_hsa_circ_320287,RMVar_hsa_circ_205078,RMVar_hsa_circ_316410,RMVar_hsa_circ_205079,RMVar_hsa_circ_205080 6375 RMVar_ID_6375 Human_SNP_ID_104769219 A-to-I Human chr2 + 183145967 183145967 183145967 CTTAAGAATTTCAAAAATCTGCTGTGCATGGTAGCTCACGCTTGGAATTGCAGCACTTTGGGAGG CTTAAGAATTTCAAAAATCTGCTGTGCATGGTGGCTCACGCTTGGAATTGCAGCACTTTGGGAGG A G NUP35 Ensembl:ENSG00000163002 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs186380763 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114739,RMVar_hsa_circ_205073,RMVar_hsa_circ_342910,RMVar_hsa_circ_60476,RMVar_hsa_circ_103366,RMVar_hsa_circ_320287,RMVar_hsa_circ_205078,RMVar_hsa_circ_316410,RMVar_hsa_circ_205079,RMVar_hsa_circ_205080 6376 RMVar_ID_6376 Human_SNP_ID_104769221 A-to-I Human chr2 + 183145972 183145972 183145972 GAATTTCAAAAATCTGCTGTGCATGGTAGCTCACGCTTGGAATTGCAGCACTTTGGGAGGCCAAG GAATTTCAAAAATCTGCTGTGCATGGTAGCTCCCGCTTGGAATTGCAGCACTTTGGGAGGCCAAG A C NUP35 Ensembl:ENSG00000163002 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs542082409 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114739,RMVar_hsa_circ_205073,RMVar_hsa_circ_342910,RMVar_hsa_circ_60476,RMVar_hsa_circ_103366,RMVar_hsa_circ_320287,RMVar_hsa_circ_205078,RMVar_hsa_circ_316410,RMVar_hsa_circ_205079,RMVar_hsa_circ_205080 6377 RMVar_ID_6377 Human_SNP_ID_104772987 A-to-I Human chr2 + 183160588 183160588 183160588 GTATTTTTAGTAGAGATGGGACCATGTTGGCCAGGGTGGTCTCAAACTTTTGACCTCAAGTAATC GTATTTTTAGTAGAGATGGGACCATGTTGGCCGGGGTGGTCTCAAACTTTTGACCTCAAGTAATC A G NUP35 Ensembl:ENSG00000163002 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs376426358 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_205081,RMVar_hsa_circ_116855,RMVar_hsa_circ_205079,RMVar_hsa_circ_205082,RMVar_hsa_circ_205083,RMVar_hsa_circ_205084 6378 RMVar_ID_6378 Human_SNP_ID_104772991 A-to-I Human chr2 + 183160617 183160617 183160617 GCCAGGGTGGTCTCAAACTTTTGACCTCAAGTAATCTGCCCACCTTGGCCTCCCAAAGTGCTGGG GCCAGGGTGGTCTCAAACTTTTGACCTCAAGTGATCTGCCCACCTTGGCCTCCCAAAGTGCTGGG A G NUP35 Ensembl:ENSG00000163002 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs763134044 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25492026 RMVar_hsa_circ_205081,RMVar_hsa_circ_116855,RMVar_hsa_circ_205079,RMVar_hsa_circ_205082,RMVar_hsa_circ_205083,RMVar_hsa_circ_205084 6379 RMVar_ID_6379 Human_SNP_ID_104772997 A-to-I Human chr2 + 183160626 183160626 183160626 GTCTCAAACTTTTGACCTCAAGTAATCTGCCCACCTTGGCCTCCCAAAGTGCTGGGATTACAGAC GTCTCAAACTTTTGACCTCAAGTAATCTGCCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGAC A G NUP35 Ensembl:ENSG00000163002 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1350534958 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25492026 RMVar_hsa_circ_205081,RMVar_hsa_circ_116855,RMVar_hsa_circ_205079,RMVar_hsa_circ_205082,RMVar_hsa_circ_205083,RMVar_hsa_circ_205084 6380 RMVar_ID_6380 Human_SNP_ID_104782980 A-to-I Human chr2 + 183199368 183199368 183199368 AAAAACAAAAACAAAAACCTCAAAATGGCTTAAAGACCTGCACATAAGACCTGAAACTACAAAAC AAAAACAAAAACAAAAACCTCAAAATGGCTTAGAGACCTGCACATAAGACCTGAAACTACAAAAC A G AC021851.1 Ensembl:ENSG00000272800 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs571935980 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2607040,Human_RBP_ID_13711050 6381 RMVar_ID_6381 Human_SNP_ID_105168832 A-to-I Human chr2 + 184739548 184739548 184739548 CCTTAGTAGCTGGGACTACAGGTGCTCACCACAAAGCCTGGCTCATTTTTTTTATTAGTAGAGAC CCTTAGTAGCTGGGACTACAGGTGCTCACCACGAAGCCTGGCTCATTTTTTTTATTAGTAGAGAC A G ZNF804A Ensembl:ENSG00000170396 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs533423840 Functional Loss SNV dbSNP153 33..33 33 - - - 6382 RMVar_ID_6382 Human_SNP_ID_105351724 A-to-I Human chr2 + 185450092 185450092 185450092 GCAATCTCGGCTCATTGCATTCTCTGCCTCCCAGATTCAAGTGATTCTCCTGCCTCAGCCTCCGG GCAATCTCGGCTCATTGCATTCTCTGCCTCCCTGATTCAAGTGATTCTCCTGCCTCAGCCTCCGG A T AC009315.1 Ensembl:ENSG00000286797 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1428348493 Functional Loss SNV dbSNP153 33..33 33 - - - 6383 RMVar_ID_6383 Human_SNP_ID_105576613 A-to-I Human chr2 - 186356908 186356908 186356908 TTGCCTAGAATTGTCTTGAACTCCTGGCTTCAAGCTATTCTCTTGCCTTTGCCTCCTAAATTGTT TTGCCTAGAATTGTCTTGAACTCCTGGCTTCAGGCTATTCTCTTGCCTTTGCCTCCTAAATTGTT T C LINC01473 Ensembl:ENSG00000237877 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs912813893 Functional Loss SNV dbSNP153 33..33 33 - - - 6384 RMVar_ID_6384 Human_SNP_ID_105618315 A-to-I Human chr2 + 186526031 186526031 186526031 TAAGACAAGTATGGCTGTGTGTGGTAGCTCACACCCATAATCCCAGCACTTCGGGAGGCCACGGC TAAGACAAGTATGGCTGTGTGTGGTAGCTCACGCCCATAATCCCAGCACTTCGGGAGGCCACGGC A G lnc-ZC3H15-2 RNACentral:URS00008B37A6 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956323535 Functional Loss SNV dbSNP153 33..33 33 - - - 6385 RMVar_ID_6385 Human_SNP_ID_105642053 A-to-I Human chr2 + 186628575 186628575 186628575 TAAGTAACTTGACCGTGGCTAACCAGCTAGTAAATAAGAGAGTATAGACCTGACACCACATGTGT TAAGTAACTTGACCGTGGCTAACCAGCTAGTAGATAAGAGAGTATAGACCTGACACCACATGTGT A G ITGAV Ensembl:ENSG00000138448 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1320920371 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1618,RMVar_hsa_circ_107753,RMVar_hsa_circ_126182,RMVar_hsa_circ_62027,RMVar_hsa_circ_37199,RMVar_hsa_circ_78211,RMVar_hsa_circ_123574,RMVar_hsa_circ_205113,RMVar_hsa_circ_205112,RMVar_hsa_circ_205118,RMVar_hsa_circ_101868,RMVar_hsa_circ_205117,RMVar_hsa_circ_205119,RMVar_hsa_circ_57753 6386 RMVar_ID_6386 Human_SNP_ID_105642061 A-to-I Human chr2 + 186628628 186628628 186628628 CACCACATGTGTCTACACCACTACACTGCACTATGTCAAATCAACAATATACTTATCATTTCCTG CACCACATGTGTCTACACCACTACACTGCACTGTGTCAAATCAACAATATACTTATCATTTCCTG A G ITGAV Ensembl:ENSG00000138448 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs186705940 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17570077,Human_RBP_ID_25492518 RMVar_hsa_circ_1618,RMVar_hsa_circ_107753,RMVar_hsa_circ_126182,RMVar_hsa_circ_62027,RMVar_hsa_circ_37199,RMVar_hsa_circ_78211,RMVar_hsa_circ_123574,RMVar_hsa_circ_205113,RMVar_hsa_circ_205112,RMVar_hsa_circ_205118,RMVar_hsa_circ_101868,RMVar_hsa_circ_205117,RMVar_hsa_circ_205119,RMVar_hsa_circ_57753 6387 RMVar_ID_6387 Human_SNP_ID_105642110 A-to-I Human chr2 + 186628874 186628874 186628874 ATTATTGATTTGAAACAGTACAGTGTAGTGTTATAGACACACCTGGGTTCAGGTCCTACTCTCTT ATTATTGATTTGAAACAGTACAGTGTAGTGTTGTAGACACACCTGGGTTCAGGTCCTACTCTCTT A G ITGAV Ensembl:ENSG00000138448 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs763845852 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569348 RMVar_hsa_circ_1618,RMVar_hsa_circ_107753,RMVar_hsa_circ_126182,RMVar_hsa_circ_62027,RMVar_hsa_circ_37199,RMVar_hsa_circ_78211,RMVar_hsa_circ_123574,RMVar_hsa_circ_205113,RMVar_hsa_circ_205112,RMVar_hsa_circ_205118,RMVar_hsa_circ_101868,RMVar_hsa_circ_205117,RMVar_hsa_circ_205119,RMVar_hsa_circ_57753 6388 RMVar_ID_6388 Human_SNP_ID_105645784 A-to-I Human chr2 + 186644037 186644037 186644037 ACAATCACAGCTCACTGCAGACTCGACTTCCCAGGCTCAAGCAATTCTCATACCTCACCCTCCCA ACAATCACAGCTCACTGCAGACTCGACTTCCCTGGCTCAAGCAATTCTCATACCTCACCCTCCCA A T ITGAV Ensembl:ENSG00000138448 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1442435183 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126182,RMVar_hsa_circ_78211,RMVar_hsa_circ_123574,RMVar_hsa_circ_205112,RMVar_hsa_circ_205118,RMVar_hsa_circ_101868,RMVar_hsa_circ_205117,RMVar_hsa_circ_369693,RMVar_hsa_circ_205119,RMVar_hsa_circ_57753,RMVar_hsa_circ_375443,RMVar_hsa_circ_315673,RMVar_hsa_circ_321664,RMVar_hsa_circ_205123,RMVar_hsa_circ_205124,RMVar_hsa_circ_205125,RMVar_hsa_circ_53738,RMVar_hsa_circ_60895,RMVar_hsa_circ_205126,RMVar_hsa_circ_54189,RMVar_hsa_circ_205128,RMVar_hsa_circ_113210,RMVar_hsa_circ_5819,RMVar_hsa_circ_6388,RMVar_hsa_circ_205129,RMVar_hsa_circ_205131,RMVar_hsa_circ_370445 6389 RMVar_ID_6389 Human_SNP_ID_105856474 A-to-I Human chr2 - 187540839 187540839 187540839 TCACCCAGGCTGGAGTGCAGTGACACAATCTCAGCTCACTACAACCTCCACCTCCTGGGATCAAA TCACCCAGGCTGGAGTGCAGTGACACAATCTCTGCTCACTACAACCTCCACCTCCTGGGATCAAA T A TFPI Ensembl:ENSG00000003436 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs892545068 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17570098 RMVar_hsa_circ_205152,RMVar_hsa_circ_124744,RMVar_hsa_circ_368194 6390 RMVar_ID_6390 Human_SNP_ID_106051145 A-to-I Human chr2 + 188354308 188354308 188354308 TTGGGTCTGGTTCCCAAACTGATGCCTACCCTACTCCCTAGGTCCAAACTTTCAGAGCATTTCTA TTGGGTCTGGTTCCCAAACTGATGCCTACCCTGCTCCCTAGGTCCAAACTTTCAGAGCATTTCTA A G GULP1 Ensembl:ENSG00000144366 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs976961090 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_205155,RMVar_hsa_circ_205156 6391 RMVar_ID_6391 Human_SNP_ID_106270178 A-to-I Human chr2 - 189285533 189285533 189285533 CTATTTCATCTCAACTTCAGTTTTCTCTTTCTATAAAATAAACATTTCTTGCCTTGCTCATCTTA CTATTTCATCTCAACTTCAGTTTTCTCTTTCTGTAAAATAAACATTTCTTGCCTTGCTCATCTTA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs745322909 Functional Loss SNV dbSNP153 33..33 33 - - - 6392 RMVar_ID_6392 Human_SNP_ID_106270183 A-to-I Human chr2 - 189285563 189285563 189285563 AGCTGTGGTATGTGACCTTCTGGAAATCAGCTATTTCATCTCAACTTCAGTTTTCTCTTTCTATA AGCTGTGGTATGTGACCTTCTGGAAATCAGCTGTTTCATCTCAACTTCAGTTTTCTCTTTCTATA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs998975580 Functional Loss SNV dbSNP153 33..33 33 - - - 6393 RMVar_ID_6393 Human_SNP_ID_106377839 A-to-I Human chr2 - 189747823 189747823 189747823 AAATTAGCCAGGTGTGGTGGCAGGCGCCTGTAACCGCAGCTACTCAAGAGGCTGAGGCAGGAGAA AAATTAGCCAGGTGTGGTGGCAGGCGCCTGTATCCGCAGCTACTCAAGAGGCTGAGGCAGGAGAA T A OSGEPL1 Ensembl:ENSG00000128694 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1313892479 Functional Loss SNV dbSNP153 33..33 33 - - - 6394 RMVar_ID_6394 Human_SNP_ID_106378326 A-to-I Human chr2 - 189750040 189750040 189750040 TTACTGCATGCAACCTCTACCTTCTGGGTTCAAGCGATTCTCCTGCTTCAGCCTCCTGAGTAGCT TTACTGCATGCAACCTCTACCTTCTGGGTTCAGGCGATTCTCCTGCTTCAGCCTCCTGAGTAGCT T C OSGEPL1 Ensembl:ENSG00000128694 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971320155 Functional Loss SNV dbSNP153 33..33 33 - - - 6395 RMVar_ID_6395 Human_SNP_ID_106378797 A-to-I Human chr2 + 189752059 189752059 189752059 CCAGCTACTCAGGAGGCTGAGGCATGACAATCACTTGAATATGGGAAGCAGAGGTTGCAGTGAGC CCAGCTACTCAGGAGGCTGAGGCATGACAATCCCTTGAATATGGGAAGCAGAGGTTGCAGTGAGC A C ANKAR Ensembl:ENSG00000151687 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs930993165 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_205323,RMVar_hsa_circ_94795 6396 RMVar_ID_6396 Human_SNP_ID_106382506 A-to-I Human chr2 - 189766642 189766642 189766642 CCAGCTCACTGCAACGTCTGCCTCCCAGGTTCAAGTGATTCTCATGCCTCAGCCTCCCACGTAGC CCAGCTCACTGCAACGTCTGCCTCCCAGGTTCCAGTGATTCTCATGCCTCAGCCTCCCACGTAGC T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1174394300 Functional Loss SNV dbSNP153 33..33 33 - - - 6397 RMVar_ID_6397 Human_SNP_ID_106386760 A-to-I Human chr2 + 189784562 189784562 189784562 CGGGTGAGACGCTGGCTGCTTGCGGCTAGTGGATGGTAATTGCCTGCCTCGCGCTAGCAGGAAGG CGGGTGAGACGCTGGCTGCTTGCGGCTAGTGGGTGGTAATTGCCTGCCTCGCGCTAGCAGGAAGG A G PMS1 Ensembl:ENSG00000064933 Protein coding 5'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053607307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_540542,Human_RBP_ID_4623764,Human_RBP_ID_18421967,Human_RBP_ID_23843947,Human_RBP_ID_27840138 Human_Splice_Rec_337269,Human_Splice_Rec_337285,Human_Splice_Rec_337307,Human_Splice_Rec_337327,Human_Splice_Rec_337347,Human_Splice_Rec_337357,Human_Splice_Rec_337363,Human_Splice_Rec_337391,Human_Splice_Rec_337413,Human_Splice_Rec_337435,Human_Splice_Rec_337443,Human_Splice_Rec_337467,Human_Splice_Rec_337493,Human_Splice_Rec_337515 6398 RMVar_ID_6398 Human_SNP_ID_106387665 A-to-I Human chr2 + 189787688 189787688 189787688 GTACATTATAGTTCTGTTGAACAGTGCTGGATAGAGTACTGGTTAAAATGGCAGGCTCTGAAATC GTACATTATAGTTCTGTTGAACAGTGCTGGATCGAGTACTGGTTAAAATGGCAGGCTCTGAAATC A C PMS1 Ensembl:ENSG00000064933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1178369981 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38332,RMVar_hsa_circ_329150,RMVar_hsa_circ_333943,RMVar_hsa_circ_39517,RMVar_hsa_circ_205328,RMVar_hsa_circ_20717 6399 RMVar_ID_6399 Human_SNP_ID_106387668 A-to-I Human chr2 + 189787702 189787702 189787702 TGTTGAACAGTGCTGGATAGAGTACTGGTTAAAATGGCAGGCTCTGAAATCACGCTACTTTGGTT TGTTGAACAGTGCTGGATAGAGTACTGGTTAAGATGGCAGGCTCTGAAATCACGCTACTTTGGTT A G PMS1 Ensembl:ENSG00000064933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs990829224 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38332,RMVar_hsa_circ_329150,RMVar_hsa_circ_333943,RMVar_hsa_circ_39517,RMVar_hsa_circ_205328,RMVar_hsa_circ_20717 6400 RMVar_ID_6400 Human_SNP_ID_106387678 A-to-I Human chr2 + 189787726 189787726 189787726 CTGGTTAAAATGGCAGGCTCTGAAATCACGCTACTTTGGTTTTATCCTAGCTCTTACTAACAGCT CTGGTTAAAATGGCAGGCTCTGAAATCACGCTGCTTTGGTTTTATCCTAGCTCTTACTAACAGCT A G PMS1 Ensembl:ENSG00000064933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs927007452 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38332,RMVar_hsa_circ_329150,RMVar_hsa_circ_333943,RMVar_hsa_circ_39517,RMVar_hsa_circ_205328,RMVar_hsa_circ_20717 6401 RMVar_ID_6401 Human_SNP_ID_106387679 A-to-I Human chr2 + 189787752 189787748 189787752 CACGCTACTTTGGTTTTATCCTAGCTCTTACTAACAGCTATATGATACTGAGGAAATTAAACTTT CACGCTACTTTGGTTTTATCCTAGCTCTT____ACAGCTATATGATACTGAGGAAATTAAACTTT TACTA T PMS1 Ensembl:ENSG00000064933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1320229918 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_38332,RMVar_hsa_circ_329150,RMVar_hsa_circ_333943,RMVar_hsa_circ_39517,RMVar_hsa_circ_205328,RMVar_hsa_circ_20717 6402 RMVar_ID_6402 Human_SNP_ID_106387687 A-to-I Human chr2 + 189787787 189787787 189787787 AGCTATATGATACTGAGGAAATTAAACTTTCTAAAACTCAATCAGCTAATCTATAAAATGGAGAC AGCTATATGATACTGAGGAAATTAAACTTTCTGAAACTCAATCAGCTAATCTATAAAATGGAGAC A G PMS1 Ensembl:ENSG00000064933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037811176 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38332,RMVar_hsa_circ_329150,RMVar_hsa_circ_333943,RMVar_hsa_circ_39517,RMVar_hsa_circ_205328,RMVar_hsa_circ_20717 6403 RMVar_ID_6403 Human_SNP_ID_106397199 A-to-I Human chr2 + 189827585 189827585 189827585 GCAGATCTCTTTGACATACTGATTTTCAACCTAAATGCCCATCAAATGATGAATGGATAAAGAAA GCAGATCTCTTTGACATACTGATTTTCAACCTCAATGCCCATCAAATGATGAATGGATAAAGAAA A C PMS1 Ensembl:ENSG00000064933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1216967207 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18312817 RMVar_hsa_circ_39517,RMVar_hsa_circ_205331,RMVar_hsa_circ_6501,RMVar_hsa_circ_287764,RMVar_hsa_circ_337115,RMVar_hsa_circ_20717,RMVar_hsa_circ_374677,RMVar_hsa_circ_332543,RMVar_hsa_circ_289507,RMVar_hsa_circ_125318,RMVar_hsa_circ_205335,RMVar_hsa_circ_205336,RMVar_hsa_circ_205333,RMVar_hsa_circ_205334,RMVar_hsa_circ_205332,RMVar_hsa_circ_73139,RMVar_hsa_circ_205329,RMVar_hsa_circ_205330,RMVar_hsa_circ_21324,RMVar_hsa_circ_348368,RMVar_hsa_circ_277493,RMVar_hsa_circ_205344,RMVar_hsa_circ_346722 6404 RMVar_ID_6404 Human_SNP_ID_106500202 A-to-I Human chr2 - 190257704 190257704 190257704 AGAAGGCCCTCGTGTGATGTTGGCACCATGATATTGGGCTTCCCAGCCTCCAGAACTGTGAGAAA AGAAGGCCCTCGTGTGATGTTGGCACCATGATTTTGGGCTTCCCAGCCTCCAGAACTGTGAGAAA T A HIBCH Ensembl:ENSG00000198130 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1023467521 Functional Loss SNV dbSNP153 33..33 33 - - - 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 6405 RMVar_ID_6405 Human_SNP_ID_106508565 A-to-I Human chr2 - 190290975 190290970 190290975 ACAGGGTGTCACTCTTCTCTCCAGGCTAGAGTACAGTGGTGTGATGATGGCTCACTGTAGCCTCA ACAGGGTGTCACTCTTCTCTCCAGGCTAGAGT_____GGTGTGATGATGGCTCACTGTAGCCTCA CACTGT C HIBCH Ensembl:ENSG00000198130 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1357994885 Functional Loss DEL dbSNP153 33..37 33 - - - 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_205360,RMVar_hsa_circ_205359,RMVar_hsa_circ_205363,RMVar_hsa_circ_12686,RMVar_hsa_circ_311649,RMVar_hsa_circ_318178,RMVar_hsa_circ_337097,RMVar_hsa_circ_354860 6406 RMVar_ID_6406 Human_SNP_ID_106526662 A-to-I Human chr2 - 190366278 190366275 190366279 AGACAGAGCGAGAGAGACAGAGAGCGAGAGAGAGACAGGAAGAGTGAAAGAGACAGAGGGAAAGA AGACAGAGCGAGAGAGACAGAGAGCGAGAGA____CAGGAAGAGTGAAAGAGACAGAGGGAAAGA GTCTC G - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs143015591 Functional Loss DEL dbSNP153 32..35 33 - - - 6407 RMVar_ID_6407 Human_SNP_ID_106582868 A-to-I Human chr2 - 190618708 190618708 190618708 GGGCTTGGTGAAACGTGCCAGTAGTCCTAGCTACTTGAGGGGCTGAGGCAGAAGGATTGCTCGAG GGGCTTGGTGAAACGTGCCAGTAGTCCTAGCTGCTTGAGGGGCTGAGGCAGAAGGATTGCTCGAG T C AC006460.2 Ensembl:ENSG00000284052 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1450403529 Functional Loss SNV dbSNP153 33..33 33 - - - 6408 RMVar_ID_6408 Human_SNP_ID_106585683 A-to-I Human chr2 - 190631974 190631974 190631974 TCAGTTCACTGCAGGCTCTACCTCCTGAGCTCAGGTGATTCTCCCACCTCAGCCTCCCGAGTAGC TCAGTTCACTGCAGGCTCTACCTCCTGAGCTCGGGTGATTCTCCCACCTCAGCCTCCCGAGTAGC T C AC006460.2 Ensembl:ENSG00000284052 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1280153374 Functional Loss SNV dbSNP153 33..33 33 - - - 6409 RMVar_ID_6409 Human_SNP_ID_106644656 A-to-I Human chr2 + 190885337 190885337 190885337 CCTCAGCCTCCCGAGTAGCTGGGATTACAGGCACCCGCCACCATGCGTGGCTAATTTTTGTTTTT CCTCAGCCTCCCGAGTAGCTGGGATTACAGGCGCCCGCCACCATGCGTGGCTAATTTTTGTTTTT A G GLS Ensembl:ENSG00000115419 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs764879956 Functional Loss SNV dbSNP153 33..33 33 - - - 6410 RMVar_ID_6410 Human_SNP_ID_106644666 A-to-I Human chr2 + 190885357 190885357 190885357 GGGATTACAGGCACCCGCCACCATGCGTGGCTAATTTTTGTTTTTAGTAGAGATGGGGTTTCACC GGGATTACAGGCACCCGCCACCATGCGTGGCTCATTTTTGTTTTTAGTAGAGATGGGGTTTCACC A C GLS Ensembl:ENSG00000115419 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs889531509 Functional Loss SNV dbSNP153 33..33 33 - - - 6411 RMVar_ID_6411 Human_SNP_ID_106644668 A-to-I Human chr2 + 190885370 190885370 190885370 CCCGCCACCATGCGTGGCTAATTTTTGTTTTTAGTAGAGATGGGGTTTCACCATGTTGGCTGGGC CCCGCCACCATGCGTGGCTAATTTTTGTTTTTGGTAGAGATGGGGTTTCACCATGTTGGCTGGGC A G GLS Ensembl:ENSG00000115419 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1389302372 Functional Loss SNV dbSNP153 33..33 33 - - - 6412 RMVar_ID_6412 Human_SNP_ID_106644838 A-to-I Human chr2 + 190886019 190886019 190886019 CTCAGCCCCCCATGTAGCTGGGACTTACAGGCACGTGCCACCACACCTGGCTAATTTTTGTATTT CTCAGCCCCCCATGTAGCTGGGACTTACAGGCCCGTGCCACCACACCTGGCTAATTTTTGTATTT A C GLS Ensembl:ENSG00000115419 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1310992433 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13720740 6413 RMVar_ID_6413 Human_SNP_ID_106644850 A-to-I Human chr2 + 190886065 190886065 190886065 CTGGCTAATTTTTGTATTTTTAGTAAGATGGGAATTTACCATGTCAGCCAGGATGGTCTCGACCT CTGGCTAATTTTTGTATTTTTAGTAAGATGGGTATTTACCATGTCAGCCAGGATGGTCTCGACCT A T GLS Ensembl:ENSG00000115419 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1192841198 Functional Loss SNV dbSNP153 33..33 33 - - - 6414 RMVar_ID_6414 Human_SNP_ID_106652411 A-to-I Human chr2 + 190917833 190917833 190917833 TTTTCTGGCTGGTCATGGTGGCTCACACCTGTAATCTCAGCACTTTGGGAGGTTGAGGTAAGAGG TTTTCTGGCTGGTCATGGTGGCTCACACCTGTGATCTCAGCACTTTGGGAGGTTGAGGTAAGAGG A G GLS Ensembl:ENSG00000115419 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1326502846 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13721494 RMVar_hsa_circ_44676,RMVar_hsa_circ_6451,RMVar_hsa_circ_72331,RMVar_hsa_circ_351484,RMVar_hsa_circ_15686,RMVar_hsa_circ_205395,RMVar_hsa_circ_205396,RMVar_hsa_circ_102168,RMVar_hsa_circ_304067,RMVar_hsa_circ_205401,RMVar_hsa_circ_205400,RMVar_hsa_circ_328624,RMVar_hsa_circ_341056,RMVar_hsa_circ_298761,RMVar_hsa_circ_293857,RMVar_hsa_circ_279266,RMVar_hsa_circ_277925,RMVar_hsa_circ_205403,RMVar_hsa_circ_205407,RMVar_hsa_circ_205405,RMVar_hsa_circ_205406,RMVar_hsa_circ_205404,RMVar_hsa_circ_74611,RMVar_hsa_circ_1242,RMVar_hsa_circ_369932,RMVar_hsa_circ_205402,RMVar_hsa_circ_205411,RMVar_hsa_circ_11773,RMVar_hsa_circ_105015,RMVar_hsa_circ_205413 6415 RMVar_ID_6415 Human_SNP_ID_106656469 A-to-I Human chr2 - 190934500 190934500 190934500 ATGCAACACAAATATGCAGTAAGGCCTTGAGAAGCATCCAGTTAGGATATGCATCTGAACATTCA ATGCAACACAAATATGCAGTAAGGCCTTGAGAGGCATCCAGTTAGGATATGCATCTGAACATTCA T C STAT1 Ensembl:ENSG00000115415 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1259299615 Functional Loss SNV dbSNP153 33..33 33 - - - 6416 RMVar_ID_6416 Human_SNP_ID_106656554 A-to-I Human chr2 + 190934865 190934865 190934865 GAGCAGAAATTTTTATAGAAAAGTATAAACGGAAGAAGAGATAAGATACTGCGAATAGGCCCTCA GAGCAGAAATTTTTATAGAAAAGTATAAACGGCAGAAGAGATAAGATACTGCGAATAGGCCCTCA A C GLS Ensembl:ENSG00000115419 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1201092197 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_540848,Human_RBP_ID_9960807,Human_RBP_ID_13721941,Human_RBP_ID_17946695,Human_RBP_ID_18312919,Human_RBP_ID_27476442 RMVar_hsa_circ_15686,RMVar_hsa_circ_328624,RMVar_hsa_circ_341056,RMVar_hsa_circ_205402,RMVar_hsa_circ_11773,RMVar_hsa_circ_205417,RMVar_hsa_circ_329139,RMVar_hsa_circ_291420,RMVar_hsa_circ_205418 6417 RMVar_ID_6417 Human_SNP_ID_106663550 A-to-I Human chr2 - 190964021 190964021 190964021 AAGGAGGACAAATCTCTTGATGCAGACTCTTAATGACAGGCTTGGAAACAAATGTTTGTTAGTTG AAGGAGGACAAATCTCTTGATGCAGACTCTTAGTGACAGGCTTGGAAACAAATGTTTGTTAGTTG T C STAT1 Ensembl:ENSG00000115415 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs971844848 Functional Loss SNV dbSNP153 33..33 33 - - - 6418 RMVar_ID_6418 Human_SNP_ID_106670488 A-to-I Human chr2 - 190992832 190992832 190992832 TGAGCCGAGATTGCGCCATTGCTCTCCAGCCTAGGAGACGGAGCAAGACTCTGTCTCAAAAAAAA TGAGCCGAGATTGCGCCATTGCTCTCCAGCCTGGGAGACGGAGCAAGACTCTGTCTCAAAAAAAA T C STAT1,RAB1AP1 Ensembl:ENSG00000115415,Ensembl:ENSG00000229023 Protein coding,Pseudogene intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1471536531 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25583888 RMVar_hsa_circ_366724,RMVar_hsa_circ_116795,RMVar_hsa_circ_40446,RMVar_hsa_circ_205424,RMVar_hsa_circ_57217,RMVar_hsa_circ_205425,RMVar_hsa_circ_127937,RMVar_hsa_circ_104634,RMVar_hsa_circ_205426,RMVar_hsa_circ_205427,RMVar_hsa_circ_120364,RMVar_hsa_circ_57746,RMVar_hsa_circ_205428,RMVar_hsa_circ_97167,RMVar_hsa_circ_368826,RMVar_hsa_circ_48494,RMVar_hsa_circ_56812,RMVar_hsa_circ_54569,RMVar_hsa_circ_64830 6419 RMVar_ID_6419 Human_SNP_ID_106675251 A-to-I Human chr2 - 191012191 191012191 191012191 CCAGGCTGGTCTTGAACTCCGGAGCTCAGGCAATCCGCCCACCTTGGCCTCCGAAAGTGCTGGGA CCAGGCTGGTCTTGAACTCCGGAGCTCAGGCAGTCCGCCCACCTTGGCCTCCGAAAGTGCTGGGA T C STAT1 Ensembl:ENSG00000115415 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs561357858 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_366724,RMVar_hsa_circ_40446,RMVar_hsa_circ_104634,RMVar_hsa_circ_205426,RMVar_hsa_circ_57746,RMVar_hsa_circ_205428,RMVar_hsa_circ_97167,RMVar_hsa_circ_48494,RMVar_hsa_circ_54569,RMVar_hsa_circ_61940,RMVar_hsa_circ_25676,RMVar_hsa_circ_327676,RMVar_hsa_circ_321839,RMVar_hsa_circ_23670,RMVar_hsa_circ_342563 6420 RMVar_ID_6420 Human_SNP_ID_106833555 A-to-I Human chr2 + 191692496 191692496 191692496 TGCAATCTCAGCTCACTGCAACCTCTGCCTCCAAGATTGAGGCGATTCTCCCACCTCAGGCTCCT TGCAATCTCAGCTCACTGCAACCTCTGCCTCCGAGATTGAGGCGATTCTCCCACCTCAGGCTCCT A G NABP1 Ensembl:ENSG00000173559 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1390313206 Functional Loss SNV dbSNP153 33..33 33 - - - 6421 RMVar_ID_6421 Human_SNP_ID_737722444 A-to-I Human chrM + 1675 1675 1675 AGATTTCAACTTAACTTGACCGCTCTGAGCTAAACCTAGCCCCAAACCCACTCCACCTTACTACC AGATTTCAACTTAACTTGACCGCTCTGAGCTAGACCTAGCCCCAAACCCACTCCACCTTACTACC A G MT-RNR2 Ensembl:ENSG00000210082 Other exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879000481 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_723288,Human_RBP_ID_1120062,Human_RBP_ID_1708771,Human_RBP_ID_2067620,Human_RBP_ID_3233460,Human_RBP_ID_3911846,Human_RBP_ID_5251956,Human_RBP_ID_5431570,Human_RBP_ID_5454865,Human_RBP_ID_5516725,Human_RBP_ID_5637185,Human_RBP_ID_7959645,Human_RBP_ID_8161410,Human_RBP_ID_8239506,Human_RBP_ID_8276579,Human_RBP_ID_8709724,Human_RBP_ID_8931288,Human_RBP_ID_9241140,Human_RBP_ID_10443873,Human_RBP_ID_16770864,Human_RBP_ID_17057544,Human_RBP_ID_17065830,Human_RBP_ID_17177685,Human_RBP_ID_17203018,Human_RBP_ID_17323982,Human_RBP_ID_17551242,Human_RBP_ID_17717159,Human_RBP_ID_18142171,Human_RBP_ID_18203787,Human_RBP_ID_18212773,Human_RBP_ID_18521659,Human_RBP_ID_18542700,Human_RBP_ID_21764563,Human_RBP_ID_21957577,Human_RBP_ID_22412291,Human_RBP_ID_22839649,Human_RBP_ID_23096004,Human_RBP_ID_24317874,Human_RBP_ID_26245925,Human_RBP_ID_26567212,Human_RBP_ID_26752570,Human_RBP_ID_27162882,Human_RBP_ID_27377499,Human_RBP_ID_27548279,Human_RBP_ID_27570829 6422 RMVar_ID_6422 Human_SNP_ID_737724385 A-to-I Human chrM + 11800 11800 11800 ACTCACAGTCGCATCATAATCCTCTCTCAAGGACTTCAAACTCTACTCCCACTAATAGCTTTTTG ACTCACAGTCGCATCATAATCCTCTCTCAAGGGCTTCAAACTCTACTCCCACTAATAGCTTTTTG A G MT-ND4 Ensembl:ENSG00000198886 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1556423995 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_271217,Human_RBP_ID_287481,Human_RBP_ID_723113,Human_RBP_ID_1228292,Human_RBP_ID_1340139,Human_RBP_ID_1404062,Human_RBP_ID_1708488,Human_RBP_ID_2067483,Human_RBP_ID_3233100,Human_RBP_ID_3911703,Human_RBP_ID_5431527,Human_RBP_ID_5482658,Human_RBP_ID_5516634,Human_RBP_ID_7959233,Human_RBP_ID_8161231,Human_RBP_ID_8276405,Human_RBP_ID_8709463,Human_RBP_ID_8931099,Human_RBP_ID_9241377,Human_RBP_ID_16770261,Human_RBP_ID_17057717,Human_RBP_ID_17202567,Human_RBP_ID_17323853,Human_RBP_ID_17439217,Human_RBP_ID_17550970,Human_RBP_ID_17717108,Human_RBP_ID_18141940,Human_RBP_ID_18203621,Human_RBP_ID_18212548,Human_RBP_ID_18521527,Human_RBP_ID_18542533,Human_RBP_ID_18912583,Human_RBP_ID_21763490,Human_RBP_ID_21957134,Human_RBP_ID_22518641,Human_RBP_ID_22839318,Human_RBP_ID_23096424,Human_RBP_ID_23201692,Human_RBP_ID_23300907,Human_RBP_ID_24317553,Human_RBP_ID_26244950,Human_RBP_ID_26566970,Human_RBP_ID_26740408,Human_RBP_ID_26752468,Human_RBP_ID_27140125,Human_RBP_ID_27162672,Human_RBP_ID_27377351,Human_RBP_ID_27548043 6423 RMVar_ID_6423 Human_SNP_ID_618509531 A-to-I Human chr17 - 15435705 15435705 15435705 TTGCTCTGTCACCCAGGCAGGAGGGCAATGGCACAACCTCTGCTCATTGCAACCTCCACTGCCAA TTGCTCTGTCACCCAGGCAGGAGGGCAATGGCGCAACCTCTGCTCATTGCAACCTCCACTGCCAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1435514537 Functional Loss SNV dbSNP153 33..33 33 - - - 6424 RMVar_ID_6424 Human_SNP_ID_618526617 A-to-I Human chr17 - 15503217 15503217 15503217 TATTTTATTTTTTGTAGAGACGGTCTCGCCACATTGCCCAGACTGGTCTGAAAGTCTTGGGCTCA TATTTTATTTTTTGTAGAGACGGTCTCGCCACTTTGCCCAGACTGGTCTGAAAGTCTTGGGCTCA T A TVP23C-CDRT4,CDRT4,TVP23C Ensembl:ENSG00000259024,Ensembl:ENSG00000239704,Ensembl:ENSG00000175106 Protein coding,Protein coding,Protein coding intron,5'UTR,CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1443481946 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2494238,Human_RBP_ID_5088285,Human_RBP_ID_12895406,Human_RBP_ID_22587645,Human_RBP_ID_24559057,Human_RBP_ID_25335322 Human_Splice_Rec_1782032,Human_Splice_Rec_1782066 6425 RMVar_ID_6425 Human_SNP_ID_618530090 A-to-I Human chr17 - 15517910 15517910 15517910 CTCCCGCCTTGGCCTCCCAAAATACTGGGATTACAGGTGTGAGCCACCGCATCTGGCTGAGGCTG CTCCCGCCTTGGCCTCCCAAAATACTGGGATTGCAGGTGTGAGCCACCGCATCTGGCTGAGGCTG T C TVP23C-CDRT4,TVP23C Ensembl:ENSG00000259024,Ensembl:ENSG00000175106 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs895690324 Functional Loss SNV dbSNP153 33..33 33 - - - 6426 RMVar_ID_6426 Human_SNP_ID_618530461 A-to-I Human chr17 - 15519438 15519438 15519438 AGATGGGGTCTTACTCTGTCACCTGGGCTGGAATGCAGTGGCATGATCATGGGTCACTGCAGCCT AGATGGGGTCTTACTCTGTCACCTGGGCTGGAGTGCAGTGGCATGATCATGGGTCACTGCAGCCT T C TVP23C-CDRT4,TVP23C Ensembl:ENSG00000259024,Ensembl:ENSG00000175106 Protein coding,Protein coding intron,intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs939400693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12895802,Human_RBP_ID_23712084 6427 RMVar_ID_6427 Human_SNP_ID_618552115 A-to-I Human chr17 - 15612318 15612318 15612318 TTTTTTTAGTAGAGGCGGGGTTTCACCGTGTTAGCCCCGATGGTCTTGATCTCCTGACCTTGTGA TTTTTTTAGTAGAGGCGGGGTTTCACCGTGTTTGCCCCGATGGTCTTGATCTCCTGACCTTGTGA T A AC005324.3,CDRT1 Ensembl:ENSG00000251537,Ensembl:ENSG00000241322 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs915122900 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_361100,RMVar_hsa_circ_362007,RMVar_hsa_circ_60520 6428 RMVar_ID_6428 Human_SNP_ID_618559260 A-to-I Human chr17 - 15639234 15639234 15639234 TGAGACCAGCCTGGGCAACGTAGTAAGCTCCTATCTCTACAAAAAATATAAAAATTAGTTGGGCA TGAGACCAGCCTGGGCAACGTAGTAAGCTCCTCTCTCTACAAAAAATATAAAAATTAGTTGGGCA T G AC005324.3,TRIM16 Ensembl:ENSG00000251537,Ensembl:ENSG00000221926 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1263459111 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60520,RMVar_hsa_circ_357695,RMVar_hsa_circ_62166,RMVar_hsa_circ_116456,RMVar_hsa_circ_345767,RMVar_hsa_circ_182219,RMVar_hsa_circ_345310 6429 RMVar_ID_6429 Human_SNP_ID_618563318 A-to-I Human chr17 - 15656807 15656807 15656807 TTGAGGCTGCAGTGAGCTGTGATTGCACCACTACGTTACAGCCTGGGCGACAAAGTTTTGAGACC TTGAGGCTGCAGTGAGCTGTGATTGCACCACTGCGTTACAGCCTGGGCGACAAAGTTTTGAGACC T C TRIM16 Ensembl:ENSG00000221926 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992113205 Functional Loss SNV dbSNP153 33..33 33 - - - 6430 RMVar_ID_6430 Human_SNP_ID_618564989 A-to-I Human chr17 - 15664499 15664499 15664499 CATCAGTGTTTTGCCCACCTTTGTTGTCACTCAAACTCCTGACCTCAAGTGATCCGCCCACCTCG CATCAGTGTTTTGCCCACCTTTGTTGTCACTCGAACTCCTGACCTCAAGTGATCCGCCCACCTCG T C TRIM16 Ensembl:ENSG00000221926 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1364343046 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12896554 RMVar_hsa_circ_303372,RMVar_hsa_circ_325632 6431 RMVar_ID_6431 Human_SNP_ID_618569268 A-to-I Human chr17 - 15683159 15683158 15683160 GGGGAAAACTTCAATCCAGAACCTCTTACCACAGTTTCTGGTAGAATGCTGGCAATTTCCAGGAA GGGGAAAACTTCAATCCAGAACCTCTTACCA__GTTTCTGGTAGAATGCTGGCAATTTCCAGGAA CTG C TRIM16 Ensembl:ENSG00000221926 Protein coding 5'UTR GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1253850152 Functional Loss DEL dbSNP153 32..33 33 - - - 6432 RMVar_ID_6432 Human_SNP_ID_618646040 A-to-I Human chr17 - 15987323 15987323 15987323 TTTGGCTCATCAGCCACCCAGGCCTTGGACCTAGTTGATCGACAGTCCATCACCTTAATCTCATC TTTGGCTCATCAGCCACCCAGGCCTTGGACCTCGTTGATCGACAGTCCATCACCTTAATCTCATC T G ZSWIM7 Ensembl:ENSG00000214941 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs751030992 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12897732,Human_RBP_ID_23712354,Human_RBP_ID_26954860 Human_Splice_Rec_1782904,Human_Splice_Rec_1782905,Human_Splice_Rec_1782914,Human_Splice_Rec_1782915,Human_Splice_Rec_1782928,Human_Splice_Rec_1782929,Human_Splice_Rec_1782936,Human_Splice_Rec_1782937,Human_Splice_Rec_1782950,Human_Splice_Rec_1782951,Human_Splice_Rec_1782962,Human_Splice_Rec_1782963,Human_Splice_Rec_1782972,Human_Splice_Rec_1782973,Human_Splice_Rec_1782980,Human_Splice_Rec_1782981,Human_Splice_Rec_1782990,Human_Splice_Rec_1782991,Human_Splice_Rec_1783000,Human_Splice_Rec_1783001,Human_Splice_Rec_1783010,Human_Splice_Rec_1783011,Human_Splice_Rec_1783018,Human_Splice_Rec_1783019,Human_Splice_Rec_1783030,Human_Splice_Rec_1783031,Human_Splice_Rec_1783042,Human_Splice_Rec_1783043,Human_Splice_Rec_1783052,Human_Splice_Rec_1783053,Human_Splice_Rec_1783058,Human_Splice_Rec_1783059,Human_Splice_Rec_1783064,Human_Splice_Rec_1783065 Human_miRNA_ID_1981168,Human_miRNA_ID_1981169,Human_miRNA_ID_1982892,Human_miRNA_ID_1982893 RMVar_hsa_circ_105153,RMVar_hsa_circ_182224,RMVar_hsa_circ_302268,RMVar_hsa_circ_292697,RMVar_hsa_circ_182226,RMVar_hsa_circ_182227,RMVar_hsa_circ_182229,RMVar_hsa_circ_182228,RMVar_hsa_circ_371830 6433 RMVar_ID_6433 Human_SNP_ID_618646930 A-to-I Human chr17 + 15991001 15991001 15991001 TCGGTGTGTGCCACCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTGGAACCTG TCGGTGTGTGCCACCTGTAGTCCCAGCTACTCTGGAGGCTGAGGCAGGAGAATCACTGGAACCTG A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1171150435 Functional Loss SNV dbSNP153 33..33 33 - - - 6434 RMVar_ID_6434 Human_SNP_ID_618646940 A-to-I Human chr17 - 15991046 15991046 15991046 TGGAGTACAGTGGCGCGATCTCAACTCACTGCAGCCTCTGCCTCCCAGGTTCCAGTGATTCTCCT TGGAGTACAGTGGCGCGATCTCAACTCACTGCCGCCTCTGCCTCCCAGGTTCCAGTGATTCTCCT T G ZSWIM7 Ensembl:ENSG00000214941 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs998709389 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1783028 RMVar_hsa_circ_105153,RMVar_hsa_circ_182227 6435 RMVar_ID_6435 Human_SNP_ID_618652850 A-to-I Human chr17 + 16013051 16013051 16013051 CATGGTGAGATCCTGTCTCTTCAAAAAATAAAAAAATTACCTGGGCACGGTGGCACATGCCTGTG CATGGTGAGATCCTGTCTCTTCAAAAAATAAACAAATTACCTGGGCACGGTGGCACATGCCTGTG A C TTC19 Ensembl:ENSG00000011295 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1289087230 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12898332,Human_RBP_ID_23308003,Human_RBP_ID_25251407 RMVar_hsa_circ_23724,RMVar_hsa_circ_22001,RMVar_hsa_circ_286109,RMVar_hsa_circ_182231,RMVar_hsa_circ_367367,RMVar_hsa_circ_341324 6436 RMVar_ID_6436 Human_SNP_ID_618653773 A-to-I Human chr17 + 16017302 16017302 16017302 ACCTTTTAAAAATTAGTGAGGCGAAAAAAATTAGCCAGGCATGGTGACGGGTGCCTATAGTCCCA ACCTTTTAAAAATTAGTGAGGCGAAAAAAATTCGCCAGGCATGGTGACGGGTGCCTATAGTCCCA A C TTC19 Ensembl:ENSG00000011295 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1343102906 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25251502 RMVar_hsa_circ_23724,RMVar_hsa_circ_22001,RMVar_hsa_circ_286109,RMVar_hsa_circ_182231,RMVar_hsa_circ_367367,RMVar_hsa_circ_341324 6437 RMVar_ID_6437 Human_SNP_ID_618654093 A-to-I Human chr17 + 16018530 16018530 16018530 TTTCTTTTGATTTGTTTTTTGTTTTTTGAGATAGGGTCTCACTGTGTCGCCCAGGCTGGAGTGCA TTTCTTTTGATTTGTTTTTTGTTTTTTGAGATGGGGTCTCACTGTGTCGCCCAGGCTGGAGTGCA A G TTC19 Ensembl:ENSG00000011295 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1354627933 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25251533 RMVar_hsa_circ_23724,RMVar_hsa_circ_22001,RMVar_hsa_circ_286109,RMVar_hsa_circ_182231,RMVar_hsa_circ_367367,RMVar_hsa_circ_341324 6438 RMVar_ID_6438 Human_SNP_ID_618654231 A-to-I Human chr17 - 16019122 16019122 16019122 CGCCATGTTGGCCAGGCTGGTCTTGAACTCCTAACCTCAGGTGATCCACCTGTCCCGGCTTCTCA CGCCATGTTGGCCAGGCTGGTCTTGAACTCCTCACCTCAGGTGATCCACCTGTCCCGGCTTCTCA T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1226145214 Functional Loss SNV dbSNP153 33..33 33 - - - 6439 RMVar_ID_6439 Human_SNP_ID_618654773 A-to-I Human chr17 - 16021206 16021206 16021206 TTTTTTTGTATTTTTATTAGAGACGGGGTTTCACAATATTTGCCAGGCTGGTCTTGAACTCCTGA TTTTTTTGTATTTTTATTAGAGACGGGGTTTCGCAATATTTGCCAGGCTGGTCTTGAACTCCTGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1207976964 Functional Loss SNV dbSNP153 33..33 33 - - - 6440 RMVar_ID_6440 Human_SNP_ID_618662767 A-to-I Human chr17 - 16050961 16050961 16050961 AGGCATGGTGGCATGCACCTGTAGTCCCAGCTACTTGGGAGCCTGAGGTGGGAGGATCACGTGAG AGGCATGGTGGCATGCACCTGTAGTCCCAGCTGCTTGGGAGCCTGAGGTGGGAGGATCACGTGAG T C NCOR1 Ensembl:ENSG00000141027 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1452519607 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32572,RMVar_hsa_circ_182243,RMVar_hsa_circ_316035,RMVar_hsa_circ_182237,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_20051,RMVar_hsa_circ_182246,RMVar_hsa_circ_348241,RMVar_hsa_circ_333492,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 6441 RMVar_ID_6441 Human_SNP_ID_618685815 A-to-I Human chr17 - 16136368 16136368 16136368 AGGCAACATAGCGAGACCCATCCTGTCTTTACAAAATAATAGAAAAAATTAGCCGGGCATGATGG AGGCAACATAGCGAGACCCATCCTGTCTTTACGAAATAATAGAAAAAATTAGCCGGGCATGATGG T C NCOR1 Ensembl:ENSG00000141027 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1437610997 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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 6442 RMVar_ID_6442 Human_SNP_ID_618685846 A-to-I Human chr17 - 16136471 16136471 16136471 AGCACTTTTTCTGTCTGGGTGTAGTGGCTCACACCTGTAATCCCCGTACTTTGGGAGGCTGGGGC AGCACTTTTTCTGTCTGGGTGTAGTGGCTCACGCCTGTAATCCCCGTACTTTGGGAGGCTGGGGC T C NCOR1 Ensembl:ENSG00000141027 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1055117145 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17565770 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_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 6443 RMVar_ID_6443 Human_SNP_ID_618697739 A-to-I Human chr17 - 16180488 16180488 16180488 CCTCAGCCTCCCAAAGTGCTAGGATTATAAGCATGAACCACTGAGCCCACCCCAGATATCTTTAT CCTCAGCCTCCCAAAGTGCTAGGATTATAAGCGTGAACCACTGAGCCCACCCCAGATATCTTTAT T C NCOR1 Ensembl:ENSG00000141027 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1371042264 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12901377 RMVar_hsa_circ_79163,RMVar_hsa_circ_182246,RMVar_hsa_circ_98921,RMVar_hsa_circ_123782,RMVar_hsa_circ_182261,RMVar_hsa_circ_182262,RMVar_hsa_circ_85654,RMVar_hsa_circ_182275,RMVar_hsa_circ_23603,RMVar_hsa_circ_17899,RMVar_hsa_circ_119362,RMVar_hsa_circ_182284,RMVar_hsa_circ_353205,RMVar_hsa_circ_339704,RMVar_hsa_circ_84455,RMVar_hsa_circ_182291,RMVar_hsa_circ_87362,RMVar_hsa_circ_81717,RMVar_hsa_circ_182303,RMVar_hsa_circ_52472,RMVar_hsa_circ_182306,RMVar_hsa_circ_289128,RMVar_hsa_circ_182305,RMVar_hsa_circ_182310,RMVar_hsa_circ_309827,RMVar_hsa_circ_285704,RMVar_hsa_circ_182311 6444 RMVar_ID_6444 Human_SNP_ID_618705635 A-to-I Human chr17 - 16208648 16208648 16208648 CAGGGTCTCATTATGTTGCTCAGGCTGACCTCAAATTGCTGGGCTCAAGTGATCCTCCCACCTTG CAGGGTCTCATTATGTTGCTCAGGCTGACCTCTAATTGCTGGGCTCAAGTGATCCTCCCACCTTG T A NCOR1 Ensembl:ENSG00000141027 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs565354338 Functional Loss SNV dbSNP153 33..33 33 - - - 6445 RMVar_ID_6445 Human_SNP_ID_618709087 A-to-I Human chr17 + 16219667 16219667 16219667 TCAGTTCACTGCAACCTACGCCTCCTGAGTTTAAGCAATTCTCTTACCTCAGCCTCTCGAGTAGC TCAGTTCACTGCAACCTACGCCTCCTGAGTTTGAGCAATTCTCTTACCTCAGCCTCTCGAGTAGC A G PIGL Ensembl:ENSG00000108474 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs764243124 Functional Loss SNV dbSNP153 33..33 33 - - - 6446 RMVar_ID_6446 Human_SNP_ID_618709728 A-to-I Human chr17 + 16221902 16221902 16221902 CGGCCTCCCAGAATGCTGGGATTACAGACGTGAGCCACCACGCCTGGCCAATTTTTGCATTTTTA CGGCCTCCCAGAATGCTGGGATTACAGACGTGTGCCACCACGCCTGGCCAATTTTTGCATTTTTA A T PIGL Ensembl:ENSG00000108474 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1568774184 Functional Loss SNV dbSNP153 33..33 33 - - - 6447 RMVar_ID_6447 Human_SNP_ID_618718088 A-to-I Human chr17 + 16256720 16256720 16256720 TTTTTGTGTGTTTGTTTGTTTGTTTGTTTTTGAGACAGGGTATCACTCTGTCACTGGAGTGCAGT TTTTTGTGTGTTTGTTTGTTTGTTTGTTTTTGCGACAGGGTATCACTCTGTCACTGGAGTGCAGT A C PIGL Ensembl:ENSG00000108474 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs550784089 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70177,RMVar_hsa_circ_66197 6448 RMVar_ID_6448 Human_SNP_ID_618721102 A-to-I Human chr17 + 16268862 16268862 16268862 TCGGCTCACTGTAGCCTCTGCCTCCAGGATTCAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGC TCGGCTCACTGTAGCCTCTGCCTCCAGGATTCTAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGC A T PIGL Ensembl:ENSG00000108474 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs767255497 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70177,RMVar_hsa_circ_66197 6449 RMVar_ID_6449 Human_SNP_ID_618729917 A-to-I Human chr17 + 16308856 16308856 16308856 CCCTCTGTTGCCCAGGCTGGAATGGTGTGATCATGGCTCACTGTAACCTTGGACCCCTGGACTCC CCCTCTGTTGCCCAGGCTGGAATGGTGTGATCCTGGCTCACTGTAACCTTGGACCCCTGGACTCC A C PIGL Ensembl:ENSG00000108474 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1018764931 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56446,RMVar_hsa_circ_66197 6450 RMVar_ID_6450 Human_SNP_ID_618729918 A-to-I Human chr17 + 16308856 16308856 16308856 CCCTCTGTTGCCCAGGCTGGAATGGTGTGATCATGGCTCACTGTAACCTTGGACCCCTGGACTCC CCCTCTGTTGCCCAGGCTGGAATGGTGTGATCGTGGCTCACTGTAACCTTGGACCCCTGGACTCC A G PIGL Ensembl:ENSG00000108474 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1018764931 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56446,RMVar_hsa_circ_66197 6451 RMVar_ID_6451 Human_SNP_ID_618738639 A-to-I Human chr17 + 16341377 16341377 16341377 GTGAGCCATGTTCATGTATTGCACTGCAGCCTAGGTGACCGAGCAAGACAGTCTCAAAATAACTA GTGAGCCATGTTCATGTATTGCACTGCAGCCTCGGTGACCGAGCAAGACAGTCTCAAAATAACTA A C PIGL Ensembl:ENSG00000108474 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs940286895 Functional Loss SNV dbSNP153 33..33 33 - - - 6452 RMVar_ID_6452 Human_SNP_ID_618740175 A-to-I Human chr17 - 16346991 16346991 16346991 AAAAAATCGGCTAGGTGTGGTGTTGCATGCCTATAGTCCCAGGTACTCGGGAGGCTGAGGTGGGA AAAAAATCGGCTAGGTGTGGTGTTGCATGCCTGTAGTCCCAGGTACTCGGGAGGCTGAGGTGGGA T C CENPV Ensembl:ENSG00000166582 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs959645526 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22475562,Human_RBP_ID_25252667 RMVar_hsa_circ_182318,RMVar_hsa_circ_99226,RMVar_hsa_circ_126839,RMVar_hsa_circ_182319,RMVar_hsa_circ_78721,RMVar_hsa_circ_340516,RMVar_hsa_circ_182320 6453 RMVar_ID_6453 Human_SNP_ID_618740187 A-to-I Human chr17 - 16347018 16347018 16347018 AGCGAGACCCCCATGTCTACAAAAAATAAAAAATCGGCTAGGTGTGGTGTTGCATGCCTATAGTC AGCGAGACCCCCATGTCTACAAAAAATAAAAAGTCGGCTAGGTGTGGTGTTGCATGCCTATAGTC T C CENPV Ensembl:ENSG00000166582 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1328117702 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12901990 RMVar_hsa_circ_182318,RMVar_hsa_circ_99226,RMVar_hsa_circ_126839,RMVar_hsa_circ_182319,RMVar_hsa_circ_78721,RMVar_hsa_circ_340516,RMVar_hsa_circ_182320 6454 RMVar_ID_6454 Human_SNP_ID_618740453 A-to-I Human chr17 - 16348294 16348294 16348294 AAATTAGCTGGGCGTTGTAGTGCATGCCTGTAATCCCAGCTACTTGGGAGGCCAAGGCAGGAGAA AAATTAGCTGGGCGTTGTAGTGCATGCCTGTAGTCCCAGCTACTTGGGAGGCCAAGGCAGGAGAA T C CENPV Ensembl:ENSG00000166582 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1490947254 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_483753 RMVar_hsa_circ_182318,RMVar_hsa_circ_99226,RMVar_hsa_circ_126839,RMVar_hsa_circ_182319,RMVar_hsa_circ_78721,RMVar_hsa_circ_340516,RMVar_hsa_circ_182320 6455 RMVar_ID_6455 Human_SNP_ID_618740457 A-to-I Human chr17 - 16348308 16348308 16348308 TACTAAAAATACAAAAATTAGCTGGGCGTTGTAGTGCATGCCTGTAATCCCAGCTACTTGGGAGG TACTAAAAATACAAAAATTAGCTGGGCGTTGTGGTGCATGCCTGTAATCCCAGCTACTTGGGAGG T C CENPV Ensembl:ENSG00000166582 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1482626574 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_483753 RMVar_hsa_circ_182318,RMVar_hsa_circ_99226,RMVar_hsa_circ_126839,RMVar_hsa_circ_182319,RMVar_hsa_circ_78721,RMVar_hsa_circ_340516,RMVar_hsa_circ_182320 6456 RMVar_ID_6456 Human_SNP_ID_618740472 A-to-I Human chr17 - 16348345 16348345 16348345 GAGGACCAGCCTGGCCAACATGGTGAAACCCTATCTCTACTAAAAATACAAAAATTAGCTGGGCG GAGGACCAGCCTGGCCAACATGGTGAAACCCTGTCTCTACTAAAAATACAAAAATTAGCTGGGCG T C CENPV Ensembl:ENSG00000166582 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs941024117 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22947302,Human_RBP_ID_25252694,Human_RBP_ID_26955092 RMVar_hsa_circ_182318,RMVar_hsa_circ_99226,RMVar_hsa_circ_126839,RMVar_hsa_circ_182319,RMVar_hsa_circ_78721,RMVar_hsa_circ_340516,RMVar_hsa_circ_182320 6457 RMVar_ID_6457 Human_SNP_ID_618743133 A-to-I Human chr17 + 16357744 16357744 16357744 TCGGCTCACTGCAACCTTTGCCTCCTGGATTCAAGCTATTCTCCTGCCTCAGCCTCTGAGTAGCT TCGGCTCACTGCAACCTTTGCCTCCTGGATTCCAGCTATTCTCCTGCCTCAGCCTCTGAGTAGCT A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1479783899 Functional Loss SNV dbSNP153 33..33 33 - - - 6458 RMVar_ID_6458 Human_SNP_ID_618749372 A-to-I Human chr17 - 16381931 16381931 16381931 GGCTCCACCTCAAGGGTGATGGTCTTGCCGGTAAGGGTTTTCACGAAGATCTGCATTTTGACCTA GGCTCCACCTCAAGGGTGATGGTCTTGCCGGTCAGGGTTTTCACGAAGATCTGCATTTTGACCTA T G - - Other Unknown GSE107867 ASD brains,cerebellum;ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs542187113 Functional Loss SNV dbSNP153 33..33 33 - - - 6459 RMVar_ID_6459 Human_SNP_ID_618749837 A-to-I Human chr17 + 16383095 16383095 16383095 AAAATTAGCTGGGCGTCGTGTCGCCTGCCTGTAGTCCCAGCTATTCGGGAGGCTGAGGCAGGAGA AAAATTAGCTGGGCGTCGTGTCGCCTGCCTGTGGTCCCAGCTATTCGGGAGGCTGAGGCAGGAGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs922956066 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26447485 6460 RMVar_ID_6460 Human_SNP_ID_618750108 A-to-I Human chr17 + 16383884 16383884 16383884 GGCACACCAGCTAATTTTTGTATTTTCAGTAGAGTTGGGGTTTTACCATGTTGACCAAGCTGGTC GGCACACCAGCTAATTTTTGTATTTTCAGTAGTGTTGGGGTTTTACCATGTTGACCAAGCTGGTC A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1396488806 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23167118,Human_RBP_ID_26447489 6461 RMVar_ID_6461 Human_SNP_ID_618763581 A-to-I Human chr17 + 16432642 16432642 16432642 TTTTTATTTTTTGTAGAGAAGAAGGTCTCACTATGTTGCCCCGGCCTCAGGTGATCCTCCCACCT TTTTTATTTTTTGTAGAGAAGAAGGTCTCACTGTGTTGCCCCGGCCTCAGGTGATCCTCCCACCT A G TRPV2 Ensembl:ENSG00000187688 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs961339121 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_372497,RMVar_hsa_circ_182329 6462 RMVar_ID_6462 Human_SNP_ID_618766417 A-to-I Human chr17 + 16441776 16441776 16441776 GACGGATTCTCTATGTTGCCCAGGCTGGTCTCAGGCTCCTGGGCTCAGATGGTCCTCCTGCCTCA GACGGATTCTCTATGTTGCCCAGGCTGGTCTCCGGCTCCTGGGCTCAGATGGTCCTCCTGCCTCA A C SNHG29 Ensembl:ENSG00000175061 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935138576 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237295,Human_RBP_ID_483876,Human_RBP_ID_766881,Human_RBP_ID_1528494,Human_RBP_ID_3513498,Human_RBP_ID_4467452,Human_RBP_ID_5088437,Human_RBP_ID_5649195,Human_RBP_ID_6563433,Human_RBP_ID_8193421,Human_RBP_ID_8254978,Human_RBP_ID_8445148,Human_RBP_ID_9069433,Human_RBP_ID_12902306,Human_RBP_ID_17258152,Human_RBP_ID_22803236,Human_RBP_ID_24414883,Human_RBP_ID_24477850,Human_RBP_ID_26447539,Human_RBP_ID_26769413,Human_RBP_ID_27250049 Human_miRNA_ID_2404376,Human_miRNA_ID_2404377,Human_miRNA_ID_2994779,Human_miRNA_ID_2994780,Human_miRNA_ID_3173656,Human_miRNA_ID_3208632 RMVar_hsa_circ_182333,RMVar_hsa_circ_78035,RMVar_hsa_circ_182334,RMVar_hsa_circ_79114 6463 RMVar_ID_6463 Human_SNP_ID_618769404 A-to-I Human chr17 + 16452593 16452593 16452593 CCAAGTAGCTGATTACAGACGCCTGCCACCACACCCCGCTAATTTTTTGTATCTTAATAGAGATG CCAAGTAGCTGATTACAGACGCCTGCCACCACGCCCCGCTAATTTTTTGTATCTTAATAGAGATG A G SNHG29 Ensembl:ENSG00000175061 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1408356934 Functional Loss SNV dbSNP153 33..33 33 - - - 6464 RMVar_ID_6464 Human_SNP_ID_618771067 A-to-I Human chr17 + 16457831 16457831 16457831 TCTACAAGAAAAAAAAAAACAAAAAATTAGCTAGGCATGGTGGTGCCTGCCTGCAGTCCCAGCTA TCTACAAGAAAAAAAAAAACAAAAAATTAGCTGGGCATGGTGGTGCCTGCCTGCAGTCCCAGCTA A G SNHG29 Ensembl:ENSG00000175061 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs961454120 Functional Loss SNV dbSNP153 33..33 33 - - - 6465 RMVar_ID_6465 Human_SNP_ID_618774062 A-to-I Human chr17 + 16470850 16470850 16470850 AAATGTATTCTCTCATAGTTTTGGAGACCAGAAATCTGAAATCAGGGTGTTGGCAGAGCTGCACT AAATGTATTCTCTCATAGTTTTGGAGACCAGATATCTGAAATCAGGGTGTTGGCAGAGCTGCACT A T SNHG29 Ensembl:ENSG00000175061 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1240148269 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1849910,Human_RBP_ID_12903467 6466 RMVar_ID_6466 Human_SNP_ID_618843198 A-to-I Human chr17 - 16772000 16772000 16772000 TTTGGTAACATACCTGCTACTTCTGCAGTTAGATCATTTTGCAACTTCTGCTGCATCTGAAATAA TTTGGTAACATACCTGCTACTTCTGCAGTTAGGTCATTTTGCAACTTCTGCTGCATCTGAAATAA T C - - Other Unknown GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1434897957 Functional Loss SNV dbSNP153 33..33 33 - - - 6467 RMVar_ID_6467 Human_SNP_ID_618889988 A-to-I Human chr17 - 16953830 16953830 16953830 GGGAGGTGGAGGTTGCTGTGAGCCAAGATCACACCCACTGCACTCCAGCCTGGGCAACAGAGAAA GGGAGGTGGAGGTTGCTGTGAGCCAAGATCACGCCCACTGCACTCCAGCCTGGGCAACAGAGAAA T C TNFRSF13B Ensembl:ENSG00000240505 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7222430 Functional Loss SNV dbSNP153 33..33 33 - - - 6468 RMVar_ID_6468 Human_SNP_ID_618890117 A-to-I Human chr17 - 16954362 16954362 16954362 TTCCTTTTTTAGAGACTGGGTCTCACTCTGTTATCCAGGCTGGAGTGCAGTGATGTGGTCATAGC TTCCTTTTTTAGAGACTGGGTCTCACTCTGTTTTCCAGGCTGGAGTGCAGTGATGTGGTCATAGC T A TNFRSF13B Ensembl:ENSG00000240505 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1334695281 Functional Loss SNV dbSNP153 33..33 33 - - - 6469 RMVar_ID_6469 Human_SNP_ID_618890152 A-to-I Human chr17 - 16954473 16954473 16954473 TGAAGATAGATGGACTTGACTGTCAGCTTTGCATGGTTTCAGGAGGGAAGGAAGATAAACCCCTG TGAAGATAGATGGACTTGACTGTCAGCTTTGCGTGGTTTCAGGAGGGAAGGAAGATAAACCCCTG T C TNFRSF13B Ensembl:ENSG00000240505 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4985783 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_290 6470 RMVar_ID_6470 Human_SNP_ID_618891467 A-to-I Human chr17 - 16960360 16960360 16960360 GCTCTGGCTAGTTCTCCTGGTGCTATGTTGAAAAGAAGTGGCAAATGTGTGTATCCTGGCCTTGT GCTCTGGCTAGTTCTCCTGGTGCTATGTTGAAGAGAAGTGGCAAATGTGTGTATCCTGGCCTTGT T C TNFRSF13B Ensembl:ENSG00000240505 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs9889948 Functional Loss SNV dbSNP153 33..33 33 - - - 6471 RMVar_ID_6471 Human_SNP_ID_618910919 A-to-I Human chr17 + 17034638 17034638 17034638 TTCTTCTTAGAATAAATTCACAGGTTGGGATTACTAGGGCAAAAGGTAAGCACATTGTTAAGGCT TTCTTCTTAGAATAAATTCACAGGTTGGGATTCCTAGGGCAAAAGGTAAGCACATTGTTAAGGCT A C AC104024.3 Ensembl:ENSG00000287114 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1235395927 Functional Loss SNV dbSNP153 33..33 33 - - - 6472 RMVar_ID_6472 Human_SNP_ID_618950779 A-to-I Human chr17 + 17186660 17186660 17186660 AGGATTGCTTGAGCCCGGGAGGTCGAGGCTGCAATCAGTCATGATCGTGTCACTGCACTCCAGCC AGGATTGCTTGAGCCCGGGAGGTCGAGGCTGCGATCAGTCATGATCGTGTCACTGCACTCCAGCC A G MPRIP Ensembl:ENSG00000133030 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs1292036489 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4408082,Human_RBP_ID_5441160,Human_RBP_ID_12905888 RMVar_hsa_circ_99099,RMVar_hsa_circ_182343,RMVar_hsa_circ_64299,RMVar_hsa_circ_120812,RMVar_hsa_circ_182374,RMVar_hsa_circ_122407,RMVar_hsa_circ_182378 6473 RMVar_ID_6473 Human_SNP_ID_618951477 A-to-I Human chr17 + 17189268 17189268 17189268 TGGAGTGTAGTGGCATGATCTCGGCTCACTGCAACCTCTGCCTCCCAGGTTCATGCCATTCTCCT TGGAGTGTAGTGGCATGATCTCGGCTCACTGCCACCTCTGCCTCCCAGGTTCATGCCATTCTCCT A C MPRIP Ensembl:ENSG00000133030 Protein coding 3'UTR GSE107867;GSE123020:GSM3490829,GSM3490830,GSM3490831 ASD brains,temporal_cortex;esophageal squamous carcinoma cells,EC109 cell line - 30559470,32596459 RNA-Seq:(High) rs998129872 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1785252 RMVar_hsa_circ_99099,RMVar_hsa_circ_182343,RMVar_hsa_circ_64299,RMVar_hsa_circ_120812,RMVar_hsa_circ_182374,RMVar_hsa_circ_122407,RMVar_hsa_circ_182378 6474 RMVar_ID_6474 Human_SNP_ID_618957800 A-to-I Human chr17 - 17210134 17210134 17210134 AAATTAGCTAGGCGTGGTGTCAGGCACCTGTAATCCCAGCTGCTCAGGAGGCTGAGGCAGGAGAA AAATTAGCTAGGCGTGGTGTCAGGCACCTGTATTCCCAGCTGCTCAGGAGGCTGAGGCAGGAGAA T A AC055811.2 Ensembl:ENSG00000264187 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1166606201 Functional Loss SNV dbSNP153 33..33 33 - - - 6475 RMVar_ID_6475 Human_SNP_ID_618957801 A-to-I Human chr17 - 17210134 17210134 17210134 AAATTAGCTAGGCGTGGTGTCAGGCACCTGTAATCCCAGCTGCTCAGGAGGCTGAGGCAGGAGAA AAATTAGCTAGGCGTGGTGTCAGGCACCTGTAGTCCCAGCTGCTCAGGAGGCTGAGGCAGGAGAA T C AC055811.2 Ensembl:ENSG00000264187 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1166606201 Functional Loss SNV dbSNP153 33..33 33 - - - 6476 RMVar_ID_6476 Human_SNP_ID_618958118 A-to-I Human chr17 - 17211147 17211147 17211147 GTAGTGCAGTGGTGTGATCTCGGCTCACTGCAAGCTCCGACTCCCTGGTTCAAGCAATTCAGCCT GTAGTGCAGTGGTGTGATCTCGGCTCACTGCAGGCTCCGACTCCCTGGTTCAAGCAATTCAGCCT T C AC055811.2 Ensembl:ENSG00000264187 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs534810007 Functional Loss SNV dbSNP153 33..33 33 - - - 6477 RMVar_ID_6477 Human_SNP_ID_618961616 A-to-I Human chr17 - 17222254 17222254 17222254 ATTGATGTGGAACTCACTTCTTCCTGGGTTCAAGTGATTCTCCTGCCCCAGCCTCCCAAGTAGCT ATTGATGTGGAACTCACTTCTTCCTGGGTTCAGGTGATTCTCCTGCCCCAGCCTCCCAAGTAGCT T C FLCN,AC055811.2 Ensembl:ENSG00000154803,Ensembl:ENSG00000264187 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs540649533 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2718,RMVar_hsa_circ_341830,RMVar_hsa_circ_10993,RMVar_hsa_circ_7049,RMVar_hsa_circ_28716,RMVar_hsa_circ_377704 6478 RMVar_ID_6478 Human_SNP_ID_618962417 A-to-I Human chr17 - 17224713 17224712 17224713 GCCAACATGGTGAAACCCCCTCTCTAAAAAAAATACAAAAAAATTAGCCAGGCGTGGTGGCACAC GCCAACATGGTGAAACCCCCTCTCTAAAAAAA_TACAAAAAAATTAGCCAGGCGTGGTGGCACAC AT A FLCN,AC055811.2 Ensembl:ENSG00000154803,Ensembl:ENSG00000264187 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs533953146 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_2718,RMVar_hsa_circ_10993,RMVar_hsa_circ_108392,RMVar_hsa_circ_7049,RMVar_hsa_circ_28716,RMVar_hsa_circ_182386,RMVar_hsa_circ_367641,RMVar_hsa_circ_370906,RMVar_hsa_circ_334202,RMVar_hsa_circ_182385,RMVar_hsa_circ_182387 6479 RMVar_ID_6479 Human_SNP_ID_618962419 A-to-I Human chr17 - 17224713 17224713 17224713 GCCAACATGGTGAAACCCCCTCTCTAAAAAAAATACAAAAAAATTAGCCAGGCGTGGTGGCACAC GCCAACATGGTGAAACCCCCTCTCTAAAAAAAGTACAAAAAAATTAGCCAGGCGTGGTGGCACAC T C FLCN,AC055811.2 Ensembl:ENSG00000154803,Ensembl:ENSG00000264187 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1228574665 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2718,RMVar_hsa_circ_10993,RMVar_hsa_circ_108392,RMVar_hsa_circ_7049,RMVar_hsa_circ_28716,RMVar_hsa_circ_182386,RMVar_hsa_circ_367641,RMVar_hsa_circ_370906,RMVar_hsa_circ_334202,RMVar_hsa_circ_182385,RMVar_hsa_circ_182387 6480 RMVar_ID_6480 Human_SNP_ID_618962580 A-to-I Human chr17 - 17225412 17225412 17225412 CACTGTGCCCCACCTTTTTAAAATTTTTTTGTAGAGATGAGGTCTCAGTATGTTGCCCAGGTTGG CACTGTGCCCCACCTTTTTAAAATTTTTTTGTGGAGATGAGGTCTCAGTATGTTGCCCAGGTTGG T C FLCN,AC055811.2 Ensembl:ENSG00000154803,Ensembl:ENSG00000264187 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285069699 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12906643,Human_RBP_ID_18690326 RMVar_hsa_circ_2718,RMVar_hsa_circ_10993,RMVar_hsa_circ_108392,RMVar_hsa_circ_7049,RMVar_hsa_circ_28716,RMVar_hsa_circ_182386,RMVar_hsa_circ_367641,RMVar_hsa_circ_370906,RMVar_hsa_circ_334202,RMVar_hsa_circ_182385,RMVar_hsa_circ_182387 6481 RMVar_ID_6481 Human_SNP_ID_618962604 A-to-I Human chr17 - 17225528 17225528 17225528 TTTTGTATTTTTAGTAGAGAAGAGATTTCACCATGTTGGCCGAGCTGGTCTTGAACTCCTGACCT TTTTGTATTTTTAGTAGAGAAGAGATTTCACCGTGTTGGCCGAGCTGGTCTTGAACTCCTGACCT T C FLCN,AC055811.2 Ensembl:ENSG00000154803,Ensembl:ENSG00000264187 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1028840799 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12906651 RMVar_hsa_circ_2718,RMVar_hsa_circ_10993,RMVar_hsa_circ_108392,RMVar_hsa_circ_7049,RMVar_hsa_circ_28716,RMVar_hsa_circ_182386,RMVar_hsa_circ_367641,RMVar_hsa_circ_370906,RMVar_hsa_circ_334202,RMVar_hsa_circ_182385,RMVar_hsa_circ_182387 6482 RMVar_ID_6482 Human_SNP_ID_618962605 A-to-I Human chr17 - 17225540 17225540 17225540 GCCCGGCTAATTTTTTGTATTTTTAGTAGAGAAGAGATTTCACCATGTTGGCCGAGCTGGTCTTG GCCCGGCTAATTTTTTGTATTTTTAGTAGAGAGGAGATTTCACCATGTTGGCCGAGCTGGTCTTG T C FLCN,AC055811.2 Ensembl:ENSG00000154803,Ensembl:ENSG00000264187 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1339746539 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12906654 RMVar_hsa_circ_2718,RMVar_hsa_circ_10993,RMVar_hsa_circ_108392,RMVar_hsa_circ_7049,RMVar_hsa_circ_28716,RMVar_hsa_circ_182386,RMVar_hsa_circ_367641,RMVar_hsa_circ_370906,RMVar_hsa_circ_334202,RMVar_hsa_circ_182385,RMVar_hsa_circ_182387 6483 RMVar_ID_6483 Human_SNP_ID_618969083 A-to-I Human chr17 - 17249359 17249359 17249359 AGAACGCACCACTGCACTCCAGCCTGGGGGACAGCGAGACTCCATCTCAAATAAATAAATAAATA AGAACGCACCACTGCACTCCAGCCTGGGGGACGGCGAGACTCCATCTCAAATAAATAAATAAATA T C COPS3 Ensembl:ENSG00000141030 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs918292832 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_30913,RMVar_hsa_circ_182391,RMVar_hsa_circ_75079,RMVar_hsa_circ_330730 6484 RMVar_ID_6484 Human_SNP_ID_618970040 A-to-I Human chr17 - 17253104 17253104 17253104 CTCTCACCTCAGCCTCCCAAGTAGCTGTGACTACAGATGTGTGCCACCACACCCAGCTAATTTTT CTCTCACCTCAGCCTCCCAAGTAGCTGTGACTGCAGATGTGTGCCACCACACCCAGCTAATTTTT T C COPS3 Ensembl:ENSG00000141030 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs554719928 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_30913,RMVar_hsa_circ_182391,RMVar_hsa_circ_75079,RMVar_hsa_circ_330730 6485 RMVar_ID_6485 Human_SNP_ID_618975418 A-to-I Human chr17 - 17273704 17273704 17273704 AGGACCACAGGTGTACACCACCACGCCCGCCTAATTTTTGTGTTTTTTTGTAAAGACAGGGTTTC AGGACCACAGGTGTACACCACCACGCCCGCCTGATTTTTGTGTTTTTTTGTAAAGACAGGGTTTC T C COPS3 Ensembl:ENSG00000141030 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1003614171 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12907568 RMVar_hsa_circ_67035,RMVar_hsa_circ_182403,RMVar_hsa_circ_323590 6486 RMVar_ID_6486 Human_SNP_ID_618975419 A-to-I Human chr17 - 17273704 17273704 17273704 AGGACCACAGGTGTACACCACCACGCCCGCCTAATTTTTGTGTTTTTTTGTAAAGACAGGGTTTC AGGACCACAGGTGTACACCACCACGCCCGCCTCATTTTTGTGTTTTTTTGTAAAGACAGGGTTTC T G COPS3 Ensembl:ENSG00000141030 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1003614171 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12907568 RMVar_hsa_circ_67035,RMVar_hsa_circ_182403,RMVar_hsa_circ_323590 6487 RMVar_ID_6487 Human_SNP_ID_618975825 A-to-I Human chr17 - 17275229 17275229 17275229 AAAACTAGCCGGGTGTGTTGGCGCATGCCTGTAGTCCCAGCTACTCAGGTGGCTGAGGCATGAGA AAAACTAGCCGGGTGTGTTGGCGCATGCCTGTGGTCCCAGCTACTCAGGTGGCTGAGGCATGAGA T C COPS3 Ensembl:ENSG00000141030 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1031139119 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67035,RMVar_hsa_circ_182403,RMVar_hsa_circ_323590 6488 RMVar_ID_6488 Human_SNP_ID_618976369 A-to-I Human chr17 - 17277583 17277583 17277583 AGACCCCTGTCTCTGCAAAAAACTTAAAAAATAAGATGGGCATGGTGACGTACACCTGTAGTTCC AGACCCCTGTCTCTGCAAAAAACTTAAAAAATCAGATGGGCATGGTGACGTACACCTGTAGTTCC T G COPS3 Ensembl:ENSG00000141030 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1295194248 Functional Loss SNV dbSNP153 33..33 33 - - - 6489 RMVar_ID_6489 Human_SNP_ID_618990613 A-to-I Human chr17 + 17331010 17331010 17331010 GGCAATCGCCTGCCTCAGCCTCCCAAAGTGCTAGGATTACAGGCGTGAGCCACTGGACCCGGCCT GGCAATCGCCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGGACCCGGCCT A G NT5M Ensembl:ENSG00000205309 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1381611950 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24577,RMVar_hsa_circ_118122,RMVar_hsa_circ_182405 6490 RMVar_ID_6490 Human_SNP_ID_619029247 A-to-I Human chr17 + 17485153 17485153 17485153 TCCGTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCACACGCCACCATGCCTTTGTAAAAAAC TCCGTGCCTCAGCCTCCCAAGTAGCTGGGACTGCAGGCACACGCCACCATGCCTTTGTAAAAAAC A G MED9 Ensembl:ENSG00000141026 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1024555710 Functional Loss SNV dbSNP153 33..33 33 - - - 6491 RMVar_ID_6491 Human_SNP_ID_619034242 A-to-I Human chr17 + 17501647 17501647 17501647 ATGATCGGGGCTGGGCGCGGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCCGAGGCGATC ATGATCGGGGCTGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGATC A G - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1279240840 Functional Loss SNV dbSNP153 33..33 33 - - - 6492 RMVar_ID_6492 Human_SNP_ID_619083565 A-to-I Human chr17 + 17688199 17688199 17688199 GGCTCCATTTCCCTCCCCTTTAAAATGAGGATAATAGGCAGGGCGCGGTGGCTTACGTCTATAAT GGCTCCATTTCCCTCCCCTTTAAAATGAGGATGATAGGCAGGGCGCGGTGGCTTACGTCTATAAT A G RAI1 Ensembl:ENSG00000108557 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749461303 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57371 6493 RMVar_ID_6493 Human_SNP_ID_619123808 A-to-I Human chr17 - 17834318 17834318 17834318 GGGAGGTCGAAGCAAGAGGATGACTTGTGTCCAGGAGTTTGAGACCAGCCTGGGCAACATGACAA GGGAGGTCGAAGCAAGAGGATGACTTGTGTCCCGGAGTTTGAGACCAGCCTGGGCAACATGACAA T G SREBF1 Ensembl:ENSG00000072310 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1467912374 Functional Loss SNV dbSNP153 33..33 33 - - - 6494 RMVar_ID_6494 Human_SNP_ID_619128408 A-to-I Human chr17 - 17852733 17852733 17852733 AGCCTCCCCAGTAGCTGGGACTACAGGCGCATACCACCACACCCAACTAATTTTGTATTTTTAGT AGCCTCCCCAGTAGCTGGGACTACAGGCGCATGCCACCACACCCAACTAATTTTGTATTTTTAGT T C TOM1L2 Ensembl:ENSG00000175662 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1473460625 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108718,RMVar_hsa_circ_182410 6495 RMVar_ID_6495 Human_SNP_ID_619129819 A-to-I Human chr17 - 17858721 17858721 17858721 AAAATTAGCTGGGCGTGGCAGCGCATGCTTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGCGA AAAATTAGCTGGGCGTGGCAGCGCATGCTTGTCATCCCAGCTACTTGGGAGGCTGAGGCAGGCGA T G TOM1L2 Ensembl:ENSG00000175662 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1409728061 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25254065 RMVar_hsa_circ_108718,RMVar_hsa_circ_182410 6496 RMVar_ID_6496 Human_SNP_ID_619129959 A-to-I Human chr17 - 17859263 17859263 17859263 CGAGACCAGCCTGACCAACATGGAGAAACCCCATCTCTACTAAAAATACAAAATTAGCTGGGCAT CGAGACCAGCCTGACCAACATGGAGAAACCCCGTCTCTACTAAAAATACAAAATTAGCTGGGCAT T C TOM1L2 Ensembl:ENSG00000175662 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1057367420 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108718,RMVar_hsa_circ_182410 6497 RMVar_ID_6497 Human_SNP_ID_619129964 A-to-I Human chr17 - 17859276 17859276 17859276 GAGGTCGGAAGTTCGAGACCAGCCTGACCAACATGGAGAAACCCCATCTCTACTAAAAATACAAA GAGGTCGGAAGTTCGAGACCAGCCTGACCAACGTGGAGAAACCCCATCTCTACTAAAAATACAAA T C TOM1L2 Ensembl:ENSG00000175662 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1044828078 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108718,RMVar_hsa_circ_182410 6498 RMVar_ID_6498 Human_SNP_ID_619129982 A-to-I Human chr17 - 17859347 17859347 17859347 GGGAAGGCTGGGCACAGTGGCTCATGCCTGTAATCTCAGCACTTTGGGAGGCCGAGGCGGGCGGA GGGAAGGCTGGGCACAGTGGCTCATGCCTGTAGTCTCAGCACTTTGGGAGGCCGAGGCGGGCGGA T C TOM1L2 Ensembl:ENSG00000175662 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1165583132 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108718,RMVar_hsa_circ_182410 6499 RMVar_ID_6499 Human_SNP_ID_619130088 A-to-I Human chr17 - 17859805 17859805 17859805 GCGATCTTGGCTCACTGCAGCTTTCCTCTCCCAGGTTCAAGCGATTGTCCTGCCTCAGCCTCCTG GCGATCTTGGCTCACTGCAGCTTTCCTCTCCCCGGTTCAAGCGATTGTCCTGCCTCAGCCTCCTG T G TOM1L2 Ensembl:ENSG00000175662 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1183893901 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108718,RMVar_hsa_circ_182410 6500 RMVar_ID_6500 Human_SNP_ID_619143951 A-to-I Human chr17 - 17916866 17916866 17916866 GGTGTGAGCCACTGTGCCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACTGTGTTGA GGTGTGAGCCACTGTGCCTGGCTAATTTTTGTGTTTTTAGTAGAGACAGGGTTTCACTGTGTTGA T C TOM1L2 Ensembl:ENSG00000175662 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037270896 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266551 6501 RMVar_ID_6501 Human_SNP_ID_619144854 A-to-I Human chr17 - 17920479 17920479 17920479 ACAAATTAGCTGGTGTGGTGACAGACACATGTAGTCCCAGCTGCTTGGGAGACTGAGGCTGGAGA ACAAATTAGCTGGTGTGGTGACAGACACATGTCGTCCCAGCTGCTTGGGAGACTGAGGCTGGAGA T G TOM1L2 Ensembl:ENSG00000175662 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1383672054 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8445743,Human_RBP_ID_12910804 RMVar_hsa_circ_266551 6502 RMVar_ID_6502 Human_SNP_ID_619152755 A-to-I Human chr17 - 17954506 17954506 17954506 TAGTTCGAGACTAGCCTGGCCAACATGGCGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCA TAGTTCGAGACTAGCCTGGCCAACATGGCGAATCCCCGTCTCTACTAAAAATACAAAAATTAGCA T A TOM1L2 Ensembl:ENSG00000175662 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1294296738 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266551 6503 RMVar_ID_6503 Human_SNP_ID_619152759 A-to-I Human chr17 - 17954516 17954516 17954516 CTGAGGTCAGTAGTTCGAGACTAGCCTGGCCAACATGGCGAAACCCCGTCTCTACTAAAAATACA CTGAGGTCAGTAGTTCGAGACTAGCCTGGCCACCATGGCGAAACCCCGTCTCTACTAAAAATACA T G TOM1L2 Ensembl:ENSG00000175662 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1568373741 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266551 6504 RMVar_ID_6504 Human_SNP_ID_619154809 A-to-I Human chr17 - 17962776 17962776 17962776 TTTTGCAATTTTAGTAGAGATAGGGTTTCACCATGTTGGCCAGGTTGGTCTCGATCTCTTGACCT TTTTGCAATTTTAGTAGAGATAGGGTTTCACCCTGTTGGCCAGGTTGGTCTCGATCTCTTGACCT T G TOM1L2 Ensembl:ENSG00000175662 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1010582849 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266551 6505 RMVar_ID_6505 Human_SNP_ID_619164698 A-to-I Human chr17 - 18003398 18003398 18003398 TCACTGCAACCTCTGCCTCCTGAGTTCAAGCAATTCTCTGCCTCAGTCTCCTGAGTAGCTAGGAT TCACTGCAACCTCTGCCTCCTGAGTTCAAGCAGTTCTCTGCCTCAGTCTCCTGAGTAGCTAGGAT T C ATPAF2 Ensembl:ENSG00000171953 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1185192848 Functional Loss SNV dbSNP153 33..33 33 - - - 6506 RMVar_ID_6506 Human_SNP_ID_619166183 A-to-I Human chr17 - 18009231 18009231 18009231 TAAATTATTATTTGTAGAGAGGGGGTCTCGCTATGTTACCCAGGCTGGTCTCAAATTCCAGGGCT TAAATTATTATTTGTAGAGAGGGGGTCTCGCTGTGTTACCCAGGCTGGTCTCAAATTCCAGGGCT T C ATPAF2 Ensembl:ENSG00000171953 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs578191122 Functional Loss SNV dbSNP153 33..33 33 - - - 6507 RMVar_ID_6507 Human_SNP_ID_619187701 A-to-I Human chr17 + 18095534 18095534 18095534 CTCCTGCCTCAGTCTCCCAAGTAGCTGGGATTACAGGCATGCACCACCCCGCCCGGCTAATTTTT CTCCTGCCTCAGTCTCCCAAGTAGCTGGGATTGCAGGCATGCACCACCCCGCCCGGCTAATTTTT A G DRG2 Ensembl:ENSG00000108591 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1263527023 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29462,RMVar_hsa_circ_80883,RMVar_hsa_circ_102789,RMVar_hsa_circ_182429,RMVar_hsa_circ_36323,RMVar_hsa_circ_182430 6508 RMVar_ID_6508 Human_SNP_ID_619214773 A-to-I Human chr17 + 18191708 18191708 18191708 ACGTGCCTCTGGGGCCGAGCATGGTGGCTCACACTTGTAATCCCAGCACTTTGGGAGGCCGAGGT ACGTGCCTCTGGGGCCGAGCATGGTGGCTCACGCTTGTAATCCCAGCACTTTGGGAGGCCGAGGT A G ALKBH5 Ensembl:ENSG00000091542 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1374370861 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_182436,RMVar_hsa_circ_109858 6509 RMVar_ID_6509 Human_SNP_ID_619215168 A-to-I Human chr17 + 18193058 18193058 18193058 TTTTTGTATTTTTGTAGAGACGGGGTTTCACCATGTCGGCCAGACTGGTTACGAACTCCTAACCT TTTTTGTATTTTTGTAGAGACGGGGTTTCACCCTGTCGGCCAGACTGGTTACGAACTCCTAACCT A C ALKBH5 Ensembl:ENSG00000091542 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1191849338 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_182436,RMVar_hsa_circ_109858 6510 RMVar_ID_6510 Human_SNP_ID_619215169 A-to-I Human chr17 + 18193058 18193058 18193058 TTTTTGTATTTTTGTAGAGACGGGGTTTCACCATGTCGGCCAGACTGGTTACGAACTCCTAACCT TTTTTGTATTTTTGTAGAGACGGGGTTTCACCGTGTCGGCCAGACTGGTTACGAACTCCTAACCT A G ALKBH5 Ensembl:ENSG00000091542 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1191849338 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_182436,RMVar_hsa_circ_109858 6511 RMVar_ID_6511 Human_SNP_ID_619215239 A-to-I Human chr17 + 18193286 18193286 18193286 AATAAAGGTTTGGGCCGGGCGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGC AATAAAGGTTTGGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGC A G ALKBH5 Ensembl:ENSG00000091542 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1013483439 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_182436,RMVar_hsa_circ_109858 6512 RMVar_ID_6512 Human_SNP_ID_619239558 A-to-I Human chr17 - 18271812 18271812 18271812 GTGATCTACCAGCCTCGGCCTCCCAAAGTGCTAGGATTAACAGGCAGGAGCCATCACACCTGGTC GTGATCTACCAGCCTCGGCCTCCCAAAGTGCTGGGATTAACAGGCAGGAGCCATCACACCTGGTC T C TOP3A Ensembl:ENSG00000177302 Protein coding intron GSE38233;GSE100210;GSE112787 cultured B-cells;HepG2 cell line;293 Flip-In T-REx cells,empty vector - 24183664,29129909,29967493 RNA-Seq:(High) rs1409333650 Functional Loss SNV dbSNP153 33..33 33 - - - 6513 RMVar_ID_6513 Human_SNP_ID_619239560 A-to-I Human chr17 - 18271819 18271819 18271819 ACCTCAGGTGATCTACCAGCCTCGGCCTCCCAAAGTGCTAGGATTAACAGGCAGGAGCCATCACA ACCTCAGGTGATCTACCAGCCTCGGCCTCCCAGAGTGCTAGGATTAACAGGCAGGAGCCATCACA T C TOP3A Ensembl:ENSG00000177302 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1396863784 Functional Loss SNV dbSNP153 33..33 33 - - - 6514 RMVar_ID_6514 Human_SNP_ID_619239580 A-to-I Human chr17 - 18271860 18271860 18271860 CGGGGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTCGTGACCTCAGGTGATCTACCAGCCTCG CGGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCGTGACCTCAGGTGATCTACCAGCCTCG T C TOP3A Ensembl:ENSG00000177302 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs963065909 Functional Loss SNV dbSNP153 33..33 33 - - - 6515 RMVar_ID_6515 Human_SNP_ID_619239581 A-to-I Human chr17 - 18271860 18271860 18271860 CGGGGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTCGTGACCTCAGGTGATCTACCAGCCTCG CGGGGTTTCACCATGTTGGCCAGGCTGGTCTCCAACTCGTGACCTCAGGTGATCTACCAGCCTCG T G TOP3A Ensembl:ENSG00000177302 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs963065909 Functional Loss SNV dbSNP153 33..33 33 - - - 6516 RMVar_ID_6516 Human_SNP_ID_619239586 A-to-I Human chr17 - 18271871 18271871 18271871 TTTAGTAAAGACGGGGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTCGTGACCTCAGGTGATC TTTAGTAAAGACGGGGTTTCACCATGTTGGCCTGGCTGGTCTCAAACTCGTGACCTCAGGTGATC T A TOP3A Ensembl:ENSG00000177302 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1167470711 Functional Loss SNV dbSNP153 33..33 33 - - - 6517 RMVar_ID_6517 Human_SNP_ID_619239594 A-to-I Human chr17 - 18271896 18271896 18271896 ACACCCAGCTAATTTGTTTAGTATTTTTAGTAAAGACGGGGTTTCACCATGTTGGCCAGGCTGGT ACACCCAGCTAATTTGTTTAGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGGT T C TOP3A Ensembl:ENSG00000177302 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1336265247 Functional Loss SNV dbSNP153 33..33 33 - - - 6518 RMVar_ID_6518 Human_SNP_ID_619239632 A-to-I Human chr17 - 18272075 18272068 18272075 GTTCTTCACCCATTTTTTATTTTTTATTTTTTATTTTTTTTTGAGATGGAGTTTCGCTCTTGTGC GTTCTTCACCCATTTTTTATTTTTTATTTTTT_______TTTGAGATGGAGTTTCGCTCTTGTGC AAAAAAAT A TOP3A Ensembl:ENSG00000177302 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs779396652 Functional Loss DEL dbSNP153 33..39 33 - - - Human_RBP_ID_6566253 6519 RMVar_ID_6519 Human_SNP_ID_619239635 A-to-I Human chr17 - 18272075 18272075 18272075 GTTCTTCACCCATTTTTTATTTTTTATTTTTTATTTTTTTTTGAGATGGAGTTTCGCTCTTGTGC GTTCTTCACCCATTTTTTATTTTTTATTTTTTTTTTTTTTTTGAGATGGAGTTTCGCTCTTGTGC T A TOP3A Ensembl:ENSG00000177302 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs531070679 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6566253 6520 RMVar_ID_6520 Human_SNP_ID_619239636 A-to-I Human chr17 - 18272082 18272082 18272082 GATTTAAGTTCTTCACCCATTTTTTATTTTTTATTTTTTATTTTTTTTTGAGATGGAGTTTCGCT GATTTAAGTTCTTCACCCATTTTTTATTTTTTGTTTTTTATTTTTTTTTGAGATGGAGTTTCGCT T C TOP3A Ensembl:ENSG00000177302 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1057082658 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6566253 6521 RMVar_ID_6521 Human_SNP_ID_619239676 A-to-I Human chr17 - 18272248 18272248 18272248 TTCCTTTCCTTTTCTTGTATTATAGCCATCCTAGTGTTTTGTCATCCTAGTGGGTATGAAGTGGC TTCCTTTCCTTTTCTTGTATTATAGCCATCCTGGTGTTTTGTCATCCTAGTGGGTATGAAGTGGC T C TOP3A Ensembl:ENSG00000177302 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs1048711418 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5274885,Human_RBP_ID_21889956 6522 RMVar_ID_6522 Human_SNP_ID_619240072 A-to-I Human chr17 - 18273902 18273902 18273902 GAATCCAACCCCGGCAGGGCGTGGAGGCTCACACCTGTAATCCAGCACTTAGGGAGGCCAAGGCT GAATCCAACCCCGGCAGGGCGTGGAGGCTCACGCCTGTAATCCAGCACTTAGGGAGGCCAAGGCT T C TOP3A Ensembl:ENSG00000177302 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1371397809 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26457161 6523 RMVar_ID_6523 Human_SNP_ID_619240119 A-to-I Human chr17 - 18274052 18274052 18274052 TGCGCCTGTAGACCCGGCTACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAACCCGGGAGGCGGA TGCGCCTGTAGACCCGGCTACTCAGGAGGCTGGGGCAGGAGAATTGCTTGAACCCGGGAGGCGGA T C TOP3A Ensembl:ENSG00000177302 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1356696223 Functional Loss SNV dbSNP153 33..33 33 - - - 6524 RMVar_ID_6524 Human_SNP_ID_619240124 A-to-I Human chr17 - 18274065 18274065 18274065 AGGTGTGGCGGTGTGCGCCTGTAGACCCGGCTACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAA AGGTGTGGCGGTGTGCGCCTGTAGACCCGGCTGCTCAGGAGGCTGAGGCAGGAGAATTGCTTGAA T C TOP3A Ensembl:ENSG00000177302 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1414634261 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12914011 6525 RMVar_ID_6525 Human_SNP_ID_619240140 A-to-I Human chr17 - 18274111 18274111 18274111 GCAACATGGTGAAACCCTGTCTCTACTAAAATACAAAAAATTAGCCAGGTGTGGCGGTGTGCGCC GCAACATGGTGAAACCCTGTCTCTACTAAAATTCAAAAAATTAGCCAGGTGTGGCGGTGTGCGCC T A TOP3A Ensembl:ENSG00000177302 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984273525 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27250658 6526 RMVar_ID_6526 Human_SNP_ID_619240141 A-to-I Human chr17 - 18274111 18274111 18274111 GCAACATGGTGAAACCCTGTCTCTACTAAAATACAAAAAATTAGCCAGGTGTGGCGGTGTGCGCC GCAACATGGTGAAACCCTGTCTCTACTAAAATGCAAAAAATTAGCCAGGTGTGGCGGTGTGCGCC T C TOP3A Ensembl:ENSG00000177302 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984273525 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27250658 6527 RMVar_ID_6527 Human_SNP_ID_619240154 A-to-I Human chr17 - 18274164 18274164 18274164 GGGAGGCTGTGGGGGGCGGATTGCCTGAGCTCAGGAGTTCGAGACCAGCCAGGGCAACATGGTGA GGGAGGCTGTGGGGGGCGGATTGCCTGAGCTCGGGAGTTCGAGACCAGCCAGGGCAACATGGTGA T C TOP3A Ensembl:ENSG00000177302 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs771904370 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25254460 6528 RMVar_ID_6528 Human_SNP_ID_619240155 A-to-I Human chr17 - 18274164 18274164 18274164 GGGAGGCTGTGGGGGGCGGATTGCCTGAGCTCAGGAGTTCGAGACCAGCCAGGGCAACATGGTGA GGGAGGCTGTGGGGGGCGGATTGCCTGAGCTCCGGAGTTCGAGACCAGCCAGGGCAACATGGTGA T G TOP3A Ensembl:ENSG00000177302 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs771904370 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25254460 6529 RMVar_ID_6529 Human_SNP_ID_619240159 A-to-I Human chr17 - 18274169 18274169 18274169 ACTTTGGGAGGCTGTGGGGGGCGGATTGCCTGAGCTCAGGAGTTCGAGACCAGCCAGGGCAACAT ACTTTGGGAGGCTGTGGGGGGCGGATTGCCTGGGCTCAGGAGTTCGAGACCAGCCAGGGCAACAT T C TOP3A Ensembl:ENSG00000177302 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs777130428 Functional Loss SNV dbSNP153 33..33 33 - - - 6530 RMVar_ID_6530 Human_SNP_ID_619241589 A-to-I Human chr17 - 18278736 18278736 18278736 TGATTTTGTGATCCGCCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTTTGAGCCACCACAC TGATTTTGTGATCCGCCCGCCTCAGCCTCCCAGAGTGCTGGGATTACAGGTTTGAGCCACCACAC T C TOP3A Ensembl:ENSG00000177302 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs934540774 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_388,RMVar_hsa_circ_371166,RMVar_hsa_circ_376134,RMVar_hsa_circ_182487,RMVar_hsa_circ_182488 6531 RMVar_ID_6531 Human_SNP_ID_619241932 A-to-I Human chr17 - 18280039 18280039 18280039 TGAAGTGATTCTTCTGCCTCAGCGTCCTGAGTAGCTGGGATTACAGGCATGCACCACTATGCCTG TGAAGTGATTCTTCTGCCTCAGCGTCCTGAGTGGCTGGGATTACAGGCATGCACCACTATGCCTG T C TOP3A Ensembl:ENSG00000177302 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs181977640 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_388,RMVar_hsa_circ_371166,RMVar_hsa_circ_376134,RMVar_hsa_circ_182487,RMVar_hsa_circ_182488 6532 RMVar_ID_6532 Human_SNP_ID_619243746 A-to-I Human chr17 - 18287153 18287153 18287153 CCTCAAACTGTCCTCCTACCTCAACCTCCCAAAGTGTTGGGATTACAGGAGTGAGCCACTGCACC CCTCAAACTGTCCTCCTACCTCAACCTCCCAAGGTGTTGGGATTACAGGAGTGAGCCACTGCACC T C TOP3A Ensembl:ENSG00000177302 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1001093512 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10483380,Human_RBP_ID_17565780 RMVar_hsa_circ_388,RMVar_hsa_circ_371166,RMVar_hsa_circ_1055,RMVar_hsa_circ_36910,RMVar_hsa_circ_340808,RMVar_hsa_circ_182487,RMVar_hsa_circ_347391,RMVar_hsa_circ_341698,RMVar_hsa_circ_333807,RMVar_hsa_circ_182493,RMVar_hsa_circ_182494,RMVar_hsa_circ_356195,RMVar_hsa_circ_320312,RMVar_hsa_circ_182495,RMVar_hsa_circ_337324,RMVar_hsa_circ_305391,RMVar_hsa_circ_16123,RMVar_hsa_circ_9346,RMVar_hsa_circ_182497,RMVar_hsa_circ_182498,RMVar_hsa_circ_182499 6533 RMVar_ID_6533 Human_SNP_ID_619243876 A-to-I Human chr17 - 18287686 18287686 18287686 CCGGCCCCTAAAAAAATTTGTTTTGGAGAGATAGCATCTTACTCTGTCACCCAGGCTAGGTCACA CCGGCCCCTAAAAAAATTTGTTTTGGAGAGATGGCATCTTACTCTGTCACCCAGGCTAGGTCACA T C TOP3A Ensembl:ENSG00000177302 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs375156472 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12914207,Human_RBP_ID_23167282 RMVar_hsa_circ_388,RMVar_hsa_circ_371166,RMVar_hsa_circ_1055,RMVar_hsa_circ_36910,RMVar_hsa_circ_340808,RMVar_hsa_circ_182487,RMVar_hsa_circ_347391,RMVar_hsa_circ_341698,RMVar_hsa_circ_333807,RMVar_hsa_circ_182493,RMVar_hsa_circ_182494,RMVar_hsa_circ_356195,RMVar_hsa_circ_320312,RMVar_hsa_circ_182495,RMVar_hsa_circ_337324,RMVar_hsa_circ_305391,RMVar_hsa_circ_16123,RMVar_hsa_circ_9346,RMVar_hsa_circ_182497,RMVar_hsa_circ_182498,RMVar_hsa_circ_182499 6534 RMVar_ID_6534 Human_SNP_ID_619246361 A-to-I Human chr17 - 18296573 18296573 18296573 TTTTGTTTGTTTGTTTGTTTGTTTTTTGAGACAGAGTCTTGCTCTGTCGCCAGGCTGGAGTGCAG TTTTGTTTGTTTGTTTGTTTGTTTTTTGAGACGGAGTCTTGCTCTGTCGCCAGGCTGGAGTGCAG T C TOP3A Ensembl:ENSG00000177302 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs949828462 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_371166,RMVar_hsa_circ_1055,RMVar_hsa_circ_36910,RMVar_hsa_circ_182487,RMVar_hsa_circ_341698,RMVar_hsa_circ_356195,RMVar_hsa_circ_182495,RMVar_hsa_circ_16123,RMVar_hsa_circ_9346,RMVar_hsa_circ_312192,RMVar_hsa_circ_182499,RMVar_hsa_circ_305656,RMVar_hsa_circ_69908,RMVar_hsa_circ_117220,RMVar_hsa_circ_37543,RMVar_hsa_circ_54695,RMVar_hsa_circ_53291,RMVar_hsa_circ_121064,RMVar_hsa_circ_182501,RMVar_hsa_circ_182502,RMVar_hsa_circ_182500,RMVar_hsa_circ_64243,RMVar_hsa_circ_35303,RMVar_hsa_circ_182505,RMVar_hsa_circ_317353,RMVar_hsa_circ_182504,RMVar_hsa_circ_182507,RMVar_hsa_circ_273006,RMVar_hsa_circ_352280,RMVar_hsa_circ_182508,RMVar_hsa_circ_6208 6535 RMVar_ID_6535 Human_SNP_ID_619247357 A-to-I Human chr17 - 18299181 18299181 18299181 CCTCAAGTGATTCTCCAGCCCCAGCCTCCCAAAGTACTGGGATTACAGGCATAAGCCACCACACC CCTCAAGTGATTCTCCAGCCCCAGCCTCCCAACGTACTGGGATTACAGGCATAAGCCACCACACC T G TOP3A Ensembl:ENSG00000177302 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1451333701 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_371166,RMVar_hsa_circ_1055,RMVar_hsa_circ_36910,RMVar_hsa_circ_182487,RMVar_hsa_circ_341698,RMVar_hsa_circ_356195,RMVar_hsa_circ_182495,RMVar_hsa_circ_16123,RMVar_hsa_circ_9346,RMVar_hsa_circ_312192,RMVar_hsa_circ_182499,RMVar_hsa_circ_305656,RMVar_hsa_circ_69908,RMVar_hsa_circ_117220,RMVar_hsa_circ_37543,RMVar_hsa_circ_54695,RMVar_hsa_circ_53291,RMVar_hsa_circ_121064,RMVar_hsa_circ_182501,RMVar_hsa_circ_182502,RMVar_hsa_circ_182500,RMVar_hsa_circ_64243,RMVar_hsa_circ_35303,RMVar_hsa_circ_182505,RMVar_hsa_circ_317353,RMVar_hsa_circ_182504,RMVar_hsa_circ_182507,RMVar_hsa_circ_273006,RMVar_hsa_circ_352280,RMVar_hsa_circ_182508,RMVar_hsa_circ_6208 6536 RMVar_ID_6536 Human_SNP_ID_619249434 A-to-I Human chr17 - 18306507 18306507 18306507 AAAAATTTAACCAGGCATGGTGATGTATGCCTATAGTCCCAGCTACTAGTAAGGCTGAGGAAGGA AAAAATTTAACCAGGCATGGTGATGTATGCCTGTAGTCCCAGCTACTAGTAAGGCTGAGGAAGGA T C TOP3A Ensembl:ENSG00000177302 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1240159261 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1055,RMVar_hsa_circ_36910,RMVar_hsa_circ_312192,RMVar_hsa_circ_117220,RMVar_hsa_circ_54695,RMVar_hsa_circ_53291,RMVar_hsa_circ_182501,RMVar_hsa_circ_182500,RMVar_hsa_circ_64243,RMVar_hsa_circ_182505,RMVar_hsa_circ_317353,RMVar_hsa_circ_182507,RMVar_hsa_circ_273006,RMVar_hsa_circ_47256,RMVar_hsa_circ_182508,RMVar_hsa_circ_291093,RMVar_hsa_circ_328604,RMVar_hsa_circ_182510,RMVar_hsa_circ_182512,RMVar_hsa_circ_318957,RMVar_hsa_circ_182513,RMVar_hsa_circ_329934,RMVar_hsa_circ_49377,RMVar_hsa_circ_288754 6537 RMVar_ID_6537 Human_SNP_ID_619249448 A-to-I Human chr17 - 18306556 18306556 18306556 TGAGACCAGCCTGGGCAACATAGTGAGACCCTATCTCTCAAAAAAAAAAAAAAATTTAACCAGGC TGAGACCAGCCTGGGCAACATAGTGAGACCCTCTCTCTCAAAAAAAAAAAAAAATTTAACCAGGC T G TOP3A Ensembl:ENSG00000177302 Protein coding intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs925051185 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25338380 RMVar_hsa_circ_1055,RMVar_hsa_circ_36910,RMVar_hsa_circ_312192,RMVar_hsa_circ_117220,RMVar_hsa_circ_54695,RMVar_hsa_circ_53291,RMVar_hsa_circ_182501,RMVar_hsa_circ_182500,RMVar_hsa_circ_64243,RMVar_hsa_circ_182505,RMVar_hsa_circ_317353,RMVar_hsa_circ_182507,RMVar_hsa_circ_273006,RMVar_hsa_circ_47256,RMVar_hsa_circ_182508,RMVar_hsa_circ_291093,RMVar_hsa_circ_328604,RMVar_hsa_circ_182510,RMVar_hsa_circ_182512,RMVar_hsa_circ_318957,RMVar_hsa_circ_182513,RMVar_hsa_circ_329934,RMVar_hsa_circ_49377,RMVar_hsa_circ_288754 6538 RMVar_ID_6538 Human_SNP_ID_619250477 A-to-I Human chr17 - 18309989 18309989 18309989 TCTATAGACATTCGCTGGGCGTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGC TCTATAGACATTCGCTGGGCGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGC T C TOP3A Ensembl:ENSG00000177302 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs974176163 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117220,RMVar_hsa_circ_182500 6539 RMVar_ID_6539 Human_SNP_ID_619254109 A-to-I Human chr17 + 18321566 18321566 18321566 CATGAGGGATGTAATAGTAGTAACTGGCCTGTACAGTGGCTCATGCCTGTAATCCCAAATCTTTG CATGAGGGATGTAATAGTAGTAACTGGCCTGTGCAGTGGCTCATGCCTGTAATCCCAAATCTTTG A G SMCR8 Ensembl:ENSG00000176994 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1357305383 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12915049 6540 RMVar_ID_6540 Human_SNP_ID_619254152 A-to-I Human chr17 + 18321709 18321709 18321709 AAAAAATTATCTGGGTGTGGTGGCATACGCCTATAGTACCAAATACTTGGGAGGCCAAGGTGGGA AAAAAATTATCTGGGTGTGGTGGCATACGCCTGTAGTACCAAATACTTGGGAGGCCAAGGTGGGA A G SMCR8 Ensembl:ENSG00000176994 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1473560823 Functional Loss SNV dbSNP153 33..33 33 - - - 6541 RMVar_ID_6541 Human_SNP_ID_619254153 A-to-I Human chr17 + 18321711 18321711 18321711 AAAATTATCTGGGTGTGGTGGCATACGCCTATAGTACCAAATACTTGGGAGGCCAAGGTGGGAGG AAAATTATCTGGGTGTGGTGGCATACGCCTATGGTACCAAATACTTGGGAGGCCAAGGTGGGAGG A G SMCR8 Ensembl:ENSG00000176994 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs932240030 Functional Loss SNV dbSNP153 33..33 33 - - - 6542 RMVar_ID_6542 Human_SNP_ID_619258055 A-to-I Human chr17 - 18336483 18336483 18336483 TTTTGTATTATTAGTAGAGACAGGGTTTCACTATGTTGACCCAGCTGGTCTTGAACTCCTGACCT TTTTGTATTATTAGTAGAGACAGGGTTTCACTGTGTTGACCCAGCTGGTCTTGAACTCCTGACCT T C SHMT1 Ensembl:ENSG00000176974 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1247837474 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72651,RMVar_hsa_circ_368027,RMVar_hsa_circ_326812,RMVar_hsa_circ_65473,RMVar_hsa_circ_66171,RMVar_hsa_circ_60812,RMVar_hsa_circ_277869,RMVar_hsa_circ_342378,RMVar_hsa_circ_365279,RMVar_hsa_circ_322602,RMVar_hsa_circ_182516,RMVar_hsa_circ_62892,RMVar_hsa_circ_322104,RMVar_hsa_circ_346427,RMVar_hsa_circ_376688,RMVar_hsa_circ_63769,RMVar_hsa_circ_182517 6543 RMVar_ID_6543 Human_SNP_ID_619259658 A-to-I Human chr17 - 18341531 18341531 18341531 GGTTCACGCCATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCGCCCGCCACCATAT GGTTCACGCCATTCTCCTGCCTCAGCCTCCCAGGTAGCTGGGATTACAGGCGCCCGCCACCATAT T C SHMT1 Ensembl:ENSG00000176974 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1272224019 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_368027,RMVar_hsa_circ_326812,RMVar_hsa_circ_66171,RMVar_hsa_circ_182519,RMVar_hsa_circ_277869,RMVar_hsa_circ_342378,RMVar_hsa_circ_322602,RMVar_hsa_circ_182516,RMVar_hsa_circ_62892,RMVar_hsa_circ_322104,RMVar_hsa_circ_346427,RMVar_hsa_circ_63769,RMVar_hsa_circ_325126,RMVar_hsa_circ_362553,RMVar_hsa_circ_182517,RMVar_hsa_circ_294671,RMVar_hsa_circ_182521,RMVar_hsa_circ_293025,RMVar_hsa_circ_182520 6544 RMVar_ID_6544 Human_SNP_ID_619259876 A-to-I Human chr17 - 18342402 18342402 18342402 CTGAGTGGGAGAATCGCTTGAGCCTGGGAGGTAGAGGTTGCAATGAGCCGAGATGGCACCACCGC CTGAGTGGGAGAATCGCTTGAGCCTGGGAGGTGGAGGTTGCAATGAGCCGAGATGGCACCACCGC T C SHMT1 Ensembl:ENSG00000176974 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs8074369 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17565783 RMVar_hsa_circ_368027,RMVar_hsa_circ_326812,RMVar_hsa_circ_66171,RMVar_hsa_circ_182519,RMVar_hsa_circ_277869,RMVar_hsa_circ_342378,RMVar_hsa_circ_322602,RMVar_hsa_circ_182516,RMVar_hsa_circ_62892,RMVar_hsa_circ_322104,RMVar_hsa_circ_346427,RMVar_hsa_circ_63769,RMVar_hsa_circ_325126,RMVar_hsa_circ_362553,RMVar_hsa_circ_182517,RMVar_hsa_circ_294671,RMVar_hsa_circ_182521,RMVar_hsa_circ_293025,RMVar_hsa_circ_182520 6545 RMVar_ID_6545 Human_SNP_ID_619260428 A-to-I Human chr17 - 18344484 18344484 18344484 TTTTTCCTTTTTGTGGAGAACAAGATCTCACTATGTTGCCCAGGCGGGTCTCAAACTCCTGGACT TTTTTCCTTTTTGTGGAGAACAAGATCTCACTGTGTTGCCCAGGCGGGTCTCAAACTCCTGGACT T C SHMT1 Ensembl:ENSG00000176974 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1246911940 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_368027,RMVar_hsa_circ_326812,RMVar_hsa_circ_66171,RMVar_hsa_circ_182519,RMVar_hsa_circ_277869,RMVar_hsa_circ_342378,RMVar_hsa_circ_322602,RMVar_hsa_circ_182516,RMVar_hsa_circ_62892,RMVar_hsa_circ_322104,RMVar_hsa_circ_346427,RMVar_hsa_circ_63769,RMVar_hsa_circ_325126,RMVar_hsa_circ_362553,RMVar_hsa_circ_182517,RMVar_hsa_circ_294671,RMVar_hsa_circ_182521,RMVar_hsa_circ_293025,RMVar_hsa_circ_182520 6546 RMVar_ID_6546 Human_SNP_ID_619262829 A-to-I Human chr17 - 18352656 18352655 18352657 ACCACCACACCCAGCTAATTTTTTGTAGAGACAGAGTTTCACCCAGGCTGTTGTTGCCCAGGCTG ACCACCACACCCAGCTAATTTTTTGTAGAGA__GAGTTTCACCCAGGCTGTTGTTGCCCAGGCTG CTG C SHMT1 Ensembl:ENSG00000176974 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1485585109 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_12915634 RMVar_hsa_circ_368027,RMVar_hsa_circ_66171,RMVar_hsa_circ_322602,RMVar_hsa_circ_62892,RMVar_hsa_circ_322104,RMVar_hsa_circ_325126,RMVar_hsa_circ_362553,RMVar_hsa_circ_182517,RMVar_hsa_circ_182521,RMVar_hsa_circ_70950,RMVar_hsa_circ_361718,RMVar_hsa_circ_328777,RMVar_hsa_circ_354852 6547 RMVar_ID_6547 Human_SNP_ID_619262837 A-to-I Human chr17 - 18352692 18352692 18352692 CCTCAGCCTACTGAGTCGCTGGGACTACAGGCACACACCACCACACCCAGCTAATTTTTTGTAGA CCTCAGCCTACTGAGTCGCTGGGACTACAGGCGCACACCACCACACCCAGCTAATTTTTTGTAGA T C SHMT1 Ensembl:ENSG00000176974 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1353253841 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_368027,RMVar_hsa_circ_66171,RMVar_hsa_circ_322602,RMVar_hsa_circ_62892,RMVar_hsa_circ_322104,RMVar_hsa_circ_325126,RMVar_hsa_circ_362553,RMVar_hsa_circ_182517,RMVar_hsa_circ_182521,RMVar_hsa_circ_70950,RMVar_hsa_circ_361718,RMVar_hsa_circ_328777,RMVar_hsa_circ_354852 6548 RMVar_ID_6548 Human_SNP_ID_619348266 A-to-I Human chr17 + 18725765 18725765 18725765 TAATCCCAGCACTTTGGGAGGCCAAGGACGGCAGATTGCTTGAGGCCAGGAGTTTGAGACCAGCC TAATCCCAGCACTTTGGGAGGCCAAGGACGGCGGATTGCTTGAGGCCAGGAGTTTGAGACCAGCC A G TRIM16L Ensembl:ENSG00000108448 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1259068936 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101043,RMVar_hsa_circ_72866,RMVar_hsa_circ_182530,RMVar_hsa_circ_76716,RMVar_hsa_circ_182532 6549 RMVar_ID_6549 Human_SNP_ID_619348277 A-to-I Human chr17 + 18725819 18725819 18725819 TGAGACCAGCCTGGGCAACGTAGTAAGCTCCTATCTCTACAAAAAATATAAAAATTAGTTGGGCA TGAGACCAGCCTGGGCAACGTAGTAAGCTCCTGTCTCTACAAAAAATATAAAAATTAGTTGGGCA A G TRIM16L Ensembl:ENSG00000108448 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1158466839 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101043,RMVar_hsa_circ_72866,RMVar_hsa_circ_182530,RMVar_hsa_circ_76716,RMVar_hsa_circ_182532 6550 RMVar_ID_6550 Human_SNP_ID_619348457 A-to-I Human chr17 + 18726536 18726536 18726536 GGGATAGGGCTGGAGTGCAGTGGCGCAATCTCAGCTCACTGCAAGCTCTGCCTCCTAGGTTCATG GGGATAGGGCTGGAGTGCAGTGGCGCAATCTCTGCTCACTGCAAGCTCTGCCTCCTAGGTTCATG A T TRIM16L Ensembl:ENSG00000108448 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs976766517 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101043,RMVar_hsa_circ_72866,RMVar_hsa_circ_182530,RMVar_hsa_circ_76716,RMVar_hsa_circ_182532 6551 RMVar_ID_6551 Human_SNP_ID_619350830 A-to-I Human chr17 + 18735671 18735671 18735671 GTTTGCAGTAATTCTTTTTTTTTTTTTTTTTGAGACGGAGTCTCGCACTGTTGCCCAGGCTGGAG GTTTGCAGTAATTCTTTTTTTTTTTTTTTTTGGGACGGAGTCTCGCACTGTTGCCCAGGCTGGAG A G TRIM16L Ensembl:ENSG00000108448 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1245047884 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101043,RMVar_hsa_circ_182530 6552 RMVar_ID_6552 Human_SNP_ID_619350831 A-to-I Human chr17 + 18735671 18735671 18735671 GTTTGCAGTAATTCTTTTTTTTTTTTTTTTTGAGACGGAGTCTCGCACTGTTGCCCAGGCTGGAG GTTTGCAGTAATTCTTTTTTTTTTTTTTTTTGTGACGGAGTCTCGCACTGTTGCCCAGGCTGGAG A T TRIM16L Ensembl:ENSG00000108448 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1245047884 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101043,RMVar_hsa_circ_182530 6553 RMVar_ID_6553 Human_SNP_ID_619362243 A-to-I Human chr17 + 18782395 18782395 18782395 GGGCGTGATGGTGCACGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAA GGGCGTGATGGTGCACGCCTGTAGTCCCAGCTGCTCGGGAGGCTGAGGCAGGAGAATCGCTTGAA A G TVP23B Ensembl:ENSG00000171928 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417407056 Functional Loss SNV dbSNP153 33..33 33 - - - 6554 RMVar_ID_6554 Human_SNP_ID_619368012 A-to-I Human chr17 + 18805782 18805782 18805782 GGGGCTAGAAAGTATGTGTTGGCACTAGAAACATTGTCAAGATTTGTTCTGTGGTGTAGGTATGC GGGGCTAGAAAGTATGTGTTGGCACTAGAAACGTTGTCAAGATTTGTTCTGTGGTGTAGGTATGC A G TVP23B Ensembl:ENSG00000171928 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1460922556 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_484620,Human_RBP_ID_1850585,Human_RBP_ID_6566889,Human_RBP_ID_13223540,Human_RBP_ID_18289542,Human_RBP_ID_26447780 Human_miRNA_ID_1203417,Human_miRNA_ID_1442035,Human_miRNA_ID_1761115 6555 RMVar_ID_6555 Human_SNP_ID_619379762 A-to-I Human chr17 + 18863329 18863329 18863329 CCGAGGCTGGTCTCAAACTCTTGGGCTCAAGCAGTCAGCCCACCTTGGCCTCACAAGGTGCTGGG CCGAGGCTGGTCTCAAACTCTTGGGCTCAAGCGGTCAGCCCACCTTGGCCTCACAAGGTGCTGGG A G PRPSAP2 Ensembl:ENSG00000141127 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs891559099 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12916167 RMVar_hsa_circ_54562,RMVar_hsa_circ_348798,RMVar_hsa_circ_362269,RMVar_hsa_circ_54643 6556 RMVar_ID_6556 Human_SNP_ID_619381163 A-to-I Human chr17 + 18868825 18868825 18868825 GCAGTTCTCCTATTTCAGCCCCCCAAAGTGCTAGGATTACAGGTGTGAGCCACCAGGCCTGGCCC GCAGTTCTCCTATTTCAGCCCCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCAGGCCTGGCCC A G PRPSAP2 Ensembl:ENSG00000141127 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1166350410 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_182552,RMVar_hsa_circ_182541,RMVar_hsa_circ_292187,RMVar_hsa_circ_348798,RMVar_hsa_circ_362269,RMVar_hsa_circ_54643,RMVar_hsa_circ_318162,RMVar_hsa_circ_319066,RMVar_hsa_circ_301908,RMVar_hsa_circ_294166,RMVar_hsa_circ_282359,RMVar_hsa_circ_270567,RMVar_hsa_circ_182545,RMVar_hsa_circ_182547,RMVar_hsa_circ_182546,RMVar_hsa_circ_182543,RMVar_hsa_circ_182544,RMVar_hsa_circ_182542,RMVar_hsa_circ_18883,RMVar_hsa_circ_61257,RMVar_hsa_circ_320604,RMVar_hsa_circ_350660,RMVar_hsa_circ_355834,RMVar_hsa_circ_51696,RMVar_hsa_circ_281478,RMVar_hsa_circ_182550,RMVar_hsa_circ_182551,RMVar_hsa_circ_315518,RMVar_hsa_circ_362933,RMVar_hsa_circ_366841,RMVar_hsa_circ_314770,RMVar_hsa_circ_182554,RMVar_hsa_circ_182555,RMVar_hsa_circ_182553 6557 RMVar_ID_6557 Human_SNP_ID_619381500 A-to-I Human chr17 + 18869947 18869947 18869947 TTGGCTCACTGCAACATCCGCCTCTCAGGTTCAAGCGATACTCCTGCCTCAGCCTCCCAAATAGG TTGGCTCACTGCAACATCCGCCTCTCAGGTTCGAGCGATACTCCTGCCTCAGCCTCCCAAATAGG A G PRPSAP2 Ensembl:ENSG00000141127 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1435464389 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_182552,RMVar_hsa_circ_182541,RMVar_hsa_circ_292187,RMVar_hsa_circ_348798,RMVar_hsa_circ_362269,RMVar_hsa_circ_54643,RMVar_hsa_circ_318162,RMVar_hsa_circ_319066,RMVar_hsa_circ_301908,RMVar_hsa_circ_294166,RMVar_hsa_circ_282359,RMVar_hsa_circ_270567,RMVar_hsa_circ_182545,RMVar_hsa_circ_182547,RMVar_hsa_circ_182546,RMVar_hsa_circ_182543,RMVar_hsa_circ_182544,RMVar_hsa_circ_182542,RMVar_hsa_circ_18883,RMVar_hsa_circ_61257,RMVar_hsa_circ_320604,RMVar_hsa_circ_350660,RMVar_hsa_circ_355834,RMVar_hsa_circ_51696,RMVar_hsa_circ_281478,RMVar_hsa_circ_182550,RMVar_hsa_circ_182551,RMVar_hsa_circ_315518,RMVar_hsa_circ_362933,RMVar_hsa_circ_366841,RMVar_hsa_circ_314770,RMVar_hsa_circ_182554,RMVar_hsa_circ_182555,RMVar_hsa_circ_182553 6558 RMVar_ID_6558 Human_SNP_ID_619384412 A-to-I Human chr17 + 18881754 18881753 18881754 CGGGGTTTTGCCATGTTCCCCAGGCTGATCTCAAACTCCTGAGCTCAAGCAGTTTGTCAGCCTTG CGGGGTTTTGCCATGTTCCCCAGGCTGATCTC_AACTCCTGAGCTCAAGCAGTTTGTCAGCCTTG CA C PRPSAP2 Ensembl:ENSG00000141127 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs930648423 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_182541,RMVar_hsa_circ_292187,RMVar_hsa_circ_348798,RMVar_hsa_circ_362269,RMVar_hsa_circ_54643,RMVar_hsa_circ_319066,RMVar_hsa_circ_301908,RMVar_hsa_circ_294166,RMVar_hsa_circ_270567,RMVar_hsa_circ_182545,RMVar_hsa_circ_182543,RMVar_hsa_circ_182544,RMVar_hsa_circ_182542,RMVar_hsa_circ_61257,RMVar_hsa_circ_320604,RMVar_hsa_circ_350660,RMVar_hsa_circ_51696,RMVar_hsa_circ_182551,RMVar_hsa_circ_315518,RMVar_hsa_circ_314770,RMVar_hsa_circ_182554,RMVar_hsa_circ_182555,RMVar_hsa_circ_288252,RMVar_hsa_circ_351172,RMVar_hsa_circ_19950,RMVar_hsa_circ_346473 6559 RMVar_ID_6559 Human_SNP_ID_619391190 A-to-I Human chr17 + 18909680 18909680 18909680 TAATTCCAGCACTTTGGGAGGCCACGGTGGGCAGATCATCTGAGGTCAGGAGTTGAAGACCAGCC TAATTCCAGCACTTTGGGAGGCCACGGTGGGCGGATCATCTGAGGTCAGGAGTTGAAGACCAGCC A G PRPSAP2 Ensembl:ENSG00000141127 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1439826540 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_182541,RMVar_hsa_circ_292187,RMVar_hsa_circ_362269,RMVar_hsa_circ_54643,RMVar_hsa_circ_301908,RMVar_hsa_circ_294166,RMVar_hsa_circ_182543,RMVar_hsa_circ_182542,RMVar_hsa_circ_350660,RMVar_hsa_circ_51696,RMVar_hsa_circ_182558,RMVar_hsa_circ_311844,RMVar_hsa_circ_19950,RMVar_hsa_circ_310516,RMVar_hsa_circ_60407,RMVar_hsa_circ_182559 6560 RMVar_ID_6560 Human_SNP_ID_619391303 A-to-I Human chr17 + 18910158 18910158 18910158 TAAGACAAAATGGCCAGGCGCAAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGTCGAGGT TAAGACAAAATGGCCAGGCGCAAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGTCGAGGT A G PRPSAP2 Ensembl:ENSG00000141127 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs942239019 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_182541,RMVar_hsa_circ_292187,RMVar_hsa_circ_362269,RMVar_hsa_circ_54643,RMVar_hsa_circ_301908,RMVar_hsa_circ_294166,RMVar_hsa_circ_182543,RMVar_hsa_circ_182542,RMVar_hsa_circ_350660,RMVar_hsa_circ_51696,RMVar_hsa_circ_182558,RMVar_hsa_circ_311844,RMVar_hsa_circ_19950,RMVar_hsa_circ_310516,RMVar_hsa_circ_60407,RMVar_hsa_circ_182559 6561 RMVar_ID_6561 Human_SNP_ID_619392151 A-to-I Human chr17 + 18913651 18913651 18913651 GCTCATTGCAGTCTCACCTCCTGGGCCCAAGCAGTCCTCCCACTTCAGCCTCATGAGTAGATGGA GCTCATTGCAGTCTCACCTCCTGGGCCCAAGCCGTCCTCCCACTTCAGCCTCATGAGTAGATGGA A C PRPSAP2 Ensembl:ENSG00000141127 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs907417765 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_182541,RMVar_hsa_circ_292187,RMVar_hsa_circ_362269,RMVar_hsa_circ_54643,RMVar_hsa_circ_294166,RMVar_hsa_circ_182542,RMVar_hsa_circ_51696,RMVar_hsa_circ_310516,RMVar_hsa_circ_60407,RMVar_hsa_circ_182559,RMVar_hsa_circ_182561,RMVar_hsa_circ_321550,RMVar_hsa_circ_373576,RMVar_hsa_circ_182560 6562 RMVar_ID_6562 Human_SNP_ID_619392161 A-to-I Human chr17 + 18913713 18913713 18913713 GGAACTACAAGCACTTGCCACCGCACCTGGCTAATTTTTGTATTTTTTGTAGAGACAAAGTTTTA GGAACTACAAGCACTTGCCACCGCACCTGGCTGATTTTTGTATTTTTTGTAGAGACAAAGTTTTA A G PRPSAP2 Ensembl:ENSG00000141127 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1368847955 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_182541,RMVar_hsa_circ_292187,RMVar_hsa_circ_362269,RMVar_hsa_circ_54643,RMVar_hsa_circ_294166,RMVar_hsa_circ_182542,RMVar_hsa_circ_51696,RMVar_hsa_circ_310516,RMVar_hsa_circ_60407,RMVar_hsa_circ_182559,RMVar_hsa_circ_182561,RMVar_hsa_circ_321550,RMVar_hsa_circ_373576,RMVar_hsa_circ_182560 6563 RMVar_ID_6563 Human_SNP_ID_619392912 A-to-I Human chr17 + 18916634 18916634 18916634 GAACCCCTGACTTCAGGTGATCCGTCCACCTCAGCCTCCCAAAGTACTGGAATTACAGGCATGAG GAACCCCTGACTTCAGGTGATCCGTCCACCTCGGCCTCCCAAAGTACTGGAATTACAGGCATGAG A G PRPSAP2 Ensembl:ENSG00000141127 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1368650039 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_182541,RMVar_hsa_circ_292187,RMVar_hsa_circ_362269,RMVar_hsa_circ_54643,RMVar_hsa_circ_294166,RMVar_hsa_circ_182542,RMVar_hsa_circ_51696,RMVar_hsa_circ_310516,RMVar_hsa_circ_60407,RMVar_hsa_circ_182559,RMVar_hsa_circ_182561,RMVar_hsa_circ_321550,RMVar_hsa_circ_373576,RMVar_hsa_circ_182560 6564 RMVar_ID_6564 Human_SNP_ID_619392917 A-to-I Human chr17 + 18916647 18916647 18916647 CAGGTGATCCGTCCACCTCAGCCTCCCAAAGTACTGGAATTACAGGCATGAGCCACTGCACCCGG CAGGTGATCCGTCCACCTCAGCCTCCCAAAGTGCTGGAATTACAGGCATGAGCCACTGCACCCGG A G PRPSAP2 Ensembl:ENSG00000141127 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1178493543 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_182541,RMVar_hsa_circ_292187,RMVar_hsa_circ_362269,RMVar_hsa_circ_54643,RMVar_hsa_circ_294166,RMVar_hsa_circ_182542,RMVar_hsa_circ_51696,RMVar_hsa_circ_310516,RMVar_hsa_circ_60407,RMVar_hsa_circ_182559,RMVar_hsa_circ_182561,RMVar_hsa_circ_321550,RMVar_hsa_circ_373576,RMVar_hsa_circ_182560 6565 RMVar_ID_6565 Human_SNP_ID_619395609 A-to-I Human chr17 + 18927912 18927912 18927912 GCAATCCTCCTGCCTCAGCCTCCCAAGTAGCTAGGACTACAGGTGCGTACCTCCATGCATGGCTA GCAATCCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGTGCGTACCTCCATGCATGGCTA A G PRPSAP2 Ensembl:ENSG00000141127 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1184610144 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_182541,RMVar_hsa_circ_292187,RMVar_hsa_circ_362269,RMVar_hsa_circ_310516,RMVar_hsa_circ_182559,RMVar_hsa_circ_321550,RMVar_hsa_circ_182563,RMVar_hsa_circ_182560,RMVar_hsa_circ_285905 6566 RMVar_ID_6566 Human_SNP_ID_619443125 A-to-I Human chr17 + 19244275 19244275 19244275 GAGGCCAGGAGTTGGAGACCAGCATGGCCAACATGGCGAAACCCCATTTCTACTAAAAATACAAA GAGGCCAGGAGTTGGAGACCAGCATGGCCAACGTGGCGAAACCCCATTTCTACTAAAAATACAAA A G EPN2 Ensembl:ENSG00000072134 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1381884311 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_182564,RMVar_hsa_circ_110734,RMVar_hsa_circ_119994,RMVar_hsa_circ_182565 6567 RMVar_ID_6567 Human_SNP_ID_619455545 A-to-I Human chr17 + 19293602 19293602 19293602 TTTTGTAGAGGTGGGGTTTTGCCACGTTGCCCAGGCTGATCTGGAACTCCTGGGCTCAAGCTATC TTTTGTAGAGGTGGGGTTTTGCCACGTTGCCCGGGCTGATCTGGAACTCCTGGGCTCAAGCTATC A G EPN2 Ensembl:ENSG00000072134 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1478023514 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12918189 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 6568 RMVar_ID_6568 Human_SNP_ID_619456162 A-to-I Human chr17 + 19295395 19295392 19295395 CACACGCGCGTGCGCGCAAAATAGCCAGGTGTAGTGGTGCATGCCTGTAGTCCCAGCTACCTGGG CACACGCGCGTGCGCGCAAAATAGCCAGGT___GTGGTGCATGCCTGTAGTCCCAGCTACCTGGG TGTA T EPN2 Ensembl:ENSG00000072134 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1314994062 Functional Loss DEL dbSNP153 31..33 33 - - - 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 6569 RMVar_ID_6569 Human_SNP_ID_619456163 A-to-I Human chr17 + 19295395 19295395 19295395 CACACGCGCGTGCGCGCAAAATAGCCAGGTGTAGTGGTGCATGCCTGTAGTCCCAGCTACCTGGG CACACGCGCGTGCGCGCAAAATAGCCAGGTGTGGTGGTGCATGCCTGTAGTCCCAGCTACCTGGG A G EPN2 Ensembl:ENSG00000072134 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs995330022 Functional Loss SNV dbSNP153 33..33 33 - - - 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 6570 RMVar_ID_6570 Human_SNP_ID_619456368 A-to-I Human chr17 + 19296174 19296174 19296174 TTCATTCTATTTTTTTTTTTTTAAACTGGGACAGAGTCTCACCCCGTCACCCAGGCTGGAGTGCA TTCATTCTATTTTTTTTTTTTTAAACTGGGACGGAGTCTCACCCCGTCACCCAGGCTGGAGTGCA A G EPN2 Ensembl:ENSG00000072134 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1245990128 Functional Loss SNV dbSNP153 33..33 33 - - - 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 6571 RMVar_ID_6571 Human_SNP_ID_619470055 A-to-I Human chr17 - 19349526 19349526 19349526 AATTTAAAAATTAGGCATGGCAGCACACGCCTATAGTCCCAGCTACTTGGGAGGCTGAGGTGGGA AATTTAAAAATTAGGCATGGCAGCACACGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGTGGGA T C B9D1 Ensembl:ENSG00000108641 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs940803556 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105448,RMVar_hsa_circ_182572 6572 RMVar_ID_6572 Human_SNP_ID_619471601 A-to-I Human chr17 - 19356229 19356229 19356229 AAATTAGCTTGGCATGGGGGTGGGCGCCTGTAATCTTAGCTACTTGGGGGGCTGAGGCAGAAGGA AAATTAGCTTGGCATGGGGGTGGGCGCCTGTAGTCTTAGCTACTTGGGGGGCTGAGGCAGAAGGA T C B9D1 Ensembl:ENSG00000108641 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982715753 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105448,RMVar_hsa_circ_182572 6573 RMVar_ID_6573 Human_SNP_ID_619476107 A-to-I Human chr17 - 19375695 19375695 19375695 CTCTATCGCCCAGGCTGGAGTGCACTGGCACGATCTCGGCTCACTGCAACATCTGCACCCCAGGT CTCTATCGCCCAGGCTGGAGTGCACTGGCACGGTCTCGGCTCACTGCAACATCTGCACCCCAGGT T C B9D1 Ensembl:ENSG00000108641 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs981274755 Functional Loss SNV dbSNP153 33..33 33 - - - 6574 RMVar_ID_6574 Human_SNP_ID_619527700 A-to-I Human chr17 + 19578057 19578057 19578057 CAGGCTGGAGTGCGGTGGTGCGATCATAGCTCACTGCAGCCTCGAACTCTTGGGCTTCAAGCAAT CAGGCTGGAGTGCGGTGGTGCGATCATAGCTCTCTGCAGCCTCGAACTCTTGGGCTTCAAGCAAT A T SLC47A1 Ensembl:ENSG00000142494 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1378684511 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_484779 Human_Splice_Rec_1791004,Human_Splice_Rec_1791005,Human_Splice_Rec_1791040,Human_Splice_Rec_1791041 6575 RMVar_ID_6575 Human_SNP_ID_619549642 A-to-I Human chr17 + 19669666 19669666 19669666 TTTCTTTTTTTTCTTGTTTGAGATAGGGTCTCACTCTGTCACCCAAGCCAGAGTACAGTGGTGCA TTTCTTTTTTTTCTTGTTTGAGATAGGGTCTCTCTCTGTCACCCAAGCCAGAGTACAGTGGTGCA A T ALDH3A2 Ensembl:ENSG00000072210 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1291189763 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12919598 RMVar_hsa_circ_279133,RMVar_hsa_circ_327040,RMVar_hsa_circ_182590,RMVar_hsa_circ_182587,RMVar_hsa_circ_288462,RMVar_hsa_circ_182591,RMVar_hsa_circ_182589,RMVar_hsa_circ_377920 6576 RMVar_ID_6576 Human_SNP_ID_619556019 A-to-I Human chr17 + 19696341 19696341 19696341 AAAATTAGCCAGGCAGAGTGGTGCGCACCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA AAAATTAGCCAGGCAGAGTGGTGCGCACCTGTGGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs563688239 Functional Loss SNV dbSNP153 33..33 33 - - - 6577 RMVar_ID_6577 Human_SNP_ID_619595920 A-to-I Human chr17 - 19847731 19847731 19847731 CAGCCTGGCCAACATGGCAAAACCCTGTCTCTACAAAAATAGAAAAATTAGCTGGGCATGGTGAT CAGCCTGGCCAACATGGCAAAACCCTGTCTCTGCAAAAATAGAAAAATTAGCTGGGCATGGTGAT T C ULK2 Ensembl:ENSG00000083290 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1206064885 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47281,RMVar_hsa_circ_1647,RMVar_hsa_circ_73729,RMVar_hsa_circ_17308,RMVar_hsa_circ_14324,RMVar_hsa_circ_370981,RMVar_hsa_circ_112718,RMVar_hsa_circ_182625,RMVar_hsa_circ_182626,RMVar_hsa_circ_325503,RMVar_hsa_circ_298994,RMVar_hsa_circ_18008,RMVar_hsa_circ_182631,RMVar_hsa_circ_182637,RMVar_hsa_circ_117391,RMVar_hsa_circ_370728,RMVar_hsa_circ_377874,RMVar_hsa_circ_182639,RMVar_hsa_circ_85187,RMVar_hsa_circ_182640,RMVar_hsa_circ_182638,RMVar_hsa_circ_182642,RMVar_hsa_circ_310872,RMVar_hsa_circ_297537,RMVar_hsa_circ_182643 6578 RMVar_ID_6578 Human_SNP_ID_619599540 A-to-I Human chr17 - 19861025 19861025 19861025 AGTCTTGCTCTTGTCGCCCAGGGTGGAGTGCAATGGCACAATCTCAGCTCATTGCACCTCTGCCT AGTCTTGCTCTTGTCGCCCAGGGTGGAGTGCAGTGGCACAATCTCAGCTCATTGCACCTCTGCCT T C ULK2 Ensembl:ENSG00000083290 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs548121291 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1792184,Human_Splice_Rec_1792185 RMVar_hsa_circ_47281,RMVar_hsa_circ_1647,RMVar_hsa_circ_73729,RMVar_hsa_circ_14324,RMVar_hsa_circ_370981,RMVar_hsa_circ_112718,RMVar_hsa_circ_182625,RMVar_hsa_circ_182626,RMVar_hsa_circ_325503,RMVar_hsa_circ_18008,RMVar_hsa_circ_117391,RMVar_hsa_circ_370728,RMVar_hsa_circ_182639,RMVar_hsa_circ_182640,RMVar_hsa_circ_4156,RMVar_hsa_circ_310872,RMVar_hsa_circ_182643 6579 RMVar_ID_6579 Human_SNP_ID_619613497 A-to-I Human chr17 - 19914559 19914559 19914559 CGACTCACTGCAGCCTCATCTTCTTGGGCTCAAATGATCCTCTCACCTCAGCCTCTCGAGTAGCT CGACTCACTGCAGCCTCATCTTCTTGGGCTCACATGATCCTCTCACCTCAGCCTCTCGAGTAGCT T G AKAP10 Ensembl:ENSG00000108599 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1468278205 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_182646,RMVar_hsa_circ_283696,RMVar_hsa_circ_337786,RMVar_hsa_circ_182644,RMVar_hsa_circ_79397,RMVar_hsa_circ_355420,RMVar_hsa_circ_377190,RMVar_hsa_circ_297786,RMVar_hsa_circ_304128,RMVar_hsa_circ_280509,RMVar_hsa_circ_182647,RMVar_hsa_circ_265687,RMVar_hsa_circ_269797,RMVar_hsa_circ_182645,RMVar_hsa_circ_269219 6580 RMVar_ID_6580 Human_SNP_ID_619614302 A-to-I Human chr17 - 19917687 19917687 19917687 CAAGTGATCCGCCCACCTTGGCCTCCCAAAGTACTGGGCTTACAGGCGTGAGCTTGTATTGGGTA CAAGTGATCCGCCCACCTTGGCCTCCCAAAGTGCTGGGCTTACAGGCGTGAGCTTGTATTGGGTA T C AKAP10 Ensembl:ENSG00000108599 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1377039136 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12920443 RMVar_hsa_circ_182646,RMVar_hsa_circ_283696,RMVar_hsa_circ_337786,RMVar_hsa_circ_182644,RMVar_hsa_circ_79397,RMVar_hsa_circ_355420,RMVar_hsa_circ_377190,RMVar_hsa_circ_297786,RMVar_hsa_circ_304128,RMVar_hsa_circ_280509,RMVar_hsa_circ_182647,RMVar_hsa_circ_265687,RMVar_hsa_circ_269797,RMVar_hsa_circ_182645,RMVar_hsa_circ_269219 6581 RMVar_ID_6581 Human_SNP_ID_619617642 A-to-I Human chr17 - 19931076 19931076 19931076 TGGAAATTCTGGGCTCAAATAATCCACCCACCACAGCCTCCTGAATAGCTGGGACTAGAGGCATG TGGAAATTCTGGGCTCAAATAATCCACCCACCGCAGCCTCCTGAATAGCTGGGACTAGAGGCATG T C AKAP10 Ensembl:ENSG00000108599 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1038780477 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25256295 RMVar_hsa_circ_182646,RMVar_hsa_circ_283696,RMVar_hsa_circ_182644,RMVar_hsa_circ_79397,RMVar_hsa_circ_355420,RMVar_hsa_circ_377190,RMVar_hsa_circ_297786,RMVar_hsa_circ_304128,RMVar_hsa_circ_182652,RMVar_hsa_circ_284441,RMVar_hsa_circ_265687,RMVar_hsa_circ_269797,RMVar_hsa_circ_182645,RMVar_hsa_circ_269219,RMVar_hsa_circ_325024,RMVar_hsa_circ_326829,RMVar_hsa_circ_331626,RMVar_hsa_circ_287014,RMVar_hsa_circ_273397,RMVar_hsa_circ_268259,RMVar_hsa_circ_182654,RMVar_hsa_circ_182655,RMVar_hsa_circ_182653,RMVar_hsa_circ_9818,RMVar_hsa_circ_318615,RMVar_hsa_circ_182650,RMVar_hsa_circ_182651,RMVar_hsa_circ_365125,RMVar_hsa_circ_338489,RMVar_hsa_circ_268751,RMVar_hsa_circ_296472,RMVar_hsa_circ_267784,RMVar_hsa_circ_182656,RMVar_hsa_circ_182658,RMVar_hsa_circ_182659,RMVar_hsa_circ_182657 6582 RMVar_ID_6582 Human_SNP_ID_619618570 A-to-I Human chr17 - 19934472 19934472 19934472 GTAGTGGCATGCACCTATAGTTCCAGCTACTCAGGAGGCTGAAGCTGGAGGATTGCATGAGCCTG GTAGTGGCATGCACCTATAGTTCCAGCTACTCCGGAGGCTGAAGCTGGAGGATTGCATGAGCCTG T G AKAP10 Ensembl:ENSG00000108599 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978760696 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_283696,RMVar_hsa_circ_182644,RMVar_hsa_circ_79397,RMVar_hsa_circ_355420,RMVar_hsa_circ_377190,RMVar_hsa_circ_304128,RMVar_hsa_circ_182652,RMVar_hsa_circ_265687,RMVar_hsa_circ_269797,RMVar_hsa_circ_182645,RMVar_hsa_circ_269219,RMVar_hsa_circ_325024,RMVar_hsa_circ_326829,RMVar_hsa_circ_331626,RMVar_hsa_circ_287014,RMVar_hsa_circ_273397,RMVar_hsa_circ_268259,RMVar_hsa_circ_182654,RMVar_hsa_circ_182655,RMVar_hsa_circ_182653,RMVar_hsa_circ_290015,RMVar_hsa_circ_9818,RMVar_hsa_circ_318615,RMVar_hsa_circ_182651,RMVar_hsa_circ_365125,RMVar_hsa_circ_338489,RMVar_hsa_circ_268751,RMVar_hsa_circ_267784,RMVar_hsa_circ_182658,RMVar_hsa_circ_182659,RMVar_hsa_circ_182657,RMVar_hsa_circ_308872,RMVar_hsa_circ_366754,RMVar_hsa_circ_313967,RMVar_hsa_circ_299553,RMVar_hsa_circ_182662,RMVar_hsa_circ_279057,RMVar_hsa_circ_182663,RMVar_hsa_circ_182660,RMVar_hsa_circ_182661 6583 RMVar_ID_6583 Human_SNP_ID_619618683 A-to-I Human chr17 - 19934925 19934925 19934925 ACACTGCAACTTCTGCCTCCCAGGTTCAACCAATTATCCTGCCTCATCCTCCCAAGTAGCTGGGA ACACTGCAACTTCTGCCTCCCAGGTTCAACCAGTTATCCTGCCTCATCCTCCCAAGTAGCTGGGA T C AKAP10 Ensembl:ENSG00000108599 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1415209937 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23308046 RMVar_hsa_circ_283696,RMVar_hsa_circ_182644,RMVar_hsa_circ_79397,RMVar_hsa_circ_355420,RMVar_hsa_circ_377190,RMVar_hsa_circ_304128,RMVar_hsa_circ_182652,RMVar_hsa_circ_265687,RMVar_hsa_circ_269797,RMVar_hsa_circ_182645,RMVar_hsa_circ_269219,RMVar_hsa_circ_325024,RMVar_hsa_circ_326829,RMVar_hsa_circ_331626,RMVar_hsa_circ_287014,RMVar_hsa_circ_273397,RMVar_hsa_circ_268259,RMVar_hsa_circ_182654,RMVar_hsa_circ_182655,RMVar_hsa_circ_182653,RMVar_hsa_circ_290015,RMVar_hsa_circ_9818,RMVar_hsa_circ_318615,RMVar_hsa_circ_182651,RMVar_hsa_circ_365125,RMVar_hsa_circ_338489,RMVar_hsa_circ_268751,RMVar_hsa_circ_267784,RMVar_hsa_circ_182658,RMVar_hsa_circ_182659,RMVar_hsa_circ_182657,RMVar_hsa_circ_308872,RMVar_hsa_circ_366754,RMVar_hsa_circ_313967,RMVar_hsa_circ_299553,RMVar_hsa_circ_182662,RMVar_hsa_circ_279057,RMVar_hsa_circ_182663,RMVar_hsa_circ_182660,RMVar_hsa_circ_182661 6584 RMVar_ID_6584 Human_SNP_ID_619618700 A-to-I Human chr17 - 19934993 19934993 19934993 TTGATTGATTGATTGAGACAGAGTTTCACTCCATTGTCCAGGCTGGAGTGCAGTTGCACAGTCTT TTGATTGATTGATTGAGACAGAGTTTCACTCCGTTGTCCAGGCTGGAGTGCAGTTGCACAGTCTT T C AKAP10 Ensembl:ENSG00000108599 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs901230886 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_283696,RMVar_hsa_circ_182644,RMVar_hsa_circ_79397,RMVar_hsa_circ_355420,RMVar_hsa_circ_377190,RMVar_hsa_circ_304128,RMVar_hsa_circ_182652,RMVar_hsa_circ_265687,RMVar_hsa_circ_269797,RMVar_hsa_circ_182645,RMVar_hsa_circ_269219,RMVar_hsa_circ_325024,RMVar_hsa_circ_326829,RMVar_hsa_circ_331626,RMVar_hsa_circ_287014,RMVar_hsa_circ_273397,RMVar_hsa_circ_268259,RMVar_hsa_circ_182654,RMVar_hsa_circ_182655,RMVar_hsa_circ_182653,RMVar_hsa_circ_290015,RMVar_hsa_circ_9818,RMVar_hsa_circ_318615,RMVar_hsa_circ_182651,RMVar_hsa_circ_365125,RMVar_hsa_circ_338489,RMVar_hsa_circ_268751,RMVar_hsa_circ_267784,RMVar_hsa_circ_182658,RMVar_hsa_circ_182659,RMVar_hsa_circ_182657,RMVar_hsa_circ_308872,RMVar_hsa_circ_366754,RMVar_hsa_circ_313967,RMVar_hsa_circ_299553,RMVar_hsa_circ_182662,RMVar_hsa_circ_279057,RMVar_hsa_circ_182663,RMVar_hsa_circ_182660,RMVar_hsa_circ_182661 6585 RMVar_ID_6585 Human_SNP_ID_619628200 A-to-I Human chr17 - 19970651 19970651 19970651 ACCCTGCTAATTCTTGTGTTTTCAGTAGAGACAGGGTTTCACCATGTTGGCAAGGCTGGTCTCGA ACCCTGCTAATTCTTGTGTTTTCAGTAGAGACGGGGTTTCACCATGTTGGCAAGGCTGGTCTCGA T C AKAP10 Ensembl:ENSG00000108599 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1377030881 Functional Loss SNV dbSNP153 33..33 33 - - - 6586 RMVar_ID_6586 Human_SNP_ID_619628201 A-to-I Human chr17 - 19970657 19970657 19970657 CACCACACCCTGCTAATTCTTGTGTTTTCAGTAGAGACAGGGTTTCACCATGTTGGCAAGGCTGG CACCACACCCTGCTAATTCTTGTGTTTTCAGTGGAGACAGGGTTTCACCATGTTGGCAAGGCTGG T C AKAP10 Ensembl:ENSG00000108599 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1304856190 Functional Loss SNV dbSNP153 33..33 33 - - - 6587 RMVar_ID_6587 Human_SNP_ID_619628873 A-to-I Human chr17 - 19973183 19973183 19973183 TTGGGGTCAGGAGTTTGAGACCAGCCTGGCCAACATGGTGAAACCCTGTCTCTACTAAAAATACA TTGGGGTCAGGAGTTTGAGACCAGCCTGGCCATCATGGTGAAACCCTGTCTCTACTAAAAATACA T A AKAP10 Ensembl:ENSG00000108599 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs770148188 Functional Loss SNV dbSNP153 33..33 33 - - - 6588 RMVar_ID_6588 Human_SNP_ID_619629106 A-to-I Human chr17 - 19974129 19974129 19974129 TGGAGTGCAGTGGCGGATCTTGGCTCACTGCAACCTCCGCCTCCTGGGTTCAAGTGATTCTCCTG TGGAGTGCAGTGGCGGATCTTGGCTCACTGCAGCCTCCGCCTCCTGGGTTCAAGTGATTCTCCTG T C AKAP10 Ensembl:ENSG00000108599 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1434378721 Functional Loss SNV dbSNP153 33..33 33 - - - 6589 RMVar_ID_6589 Human_SNP_ID_619629366 A-to-I Human chr17 - 19975298 19975298 19975298 CTAATGCCGAGATGCCAAACATGGTGGTTCATATCTGTAATCCCAGTATTTTAGGAGGCCGAGGC CTAATGCCGAGATGCCAAACATGGTGGTTCATGTCTGTAATCCCAGTATTTTAGGAGGCCGAGGC T C AKAP10 Ensembl:ENSG00000108599 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs527710687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12921870,Human_RBP_ID_25256556 6590 RMVar_ID_6590 Human_SNP_ID_619665920 A-to-I Human chr17 + 20116085 20116076 20116085 CTATAATATATCAATAACTTTCTTTTTTATTTATTTTATTTATTTATTTTTTTGAGATGGAGTCT CTATAATATATCAATAACTTTCTT_________TTTTATTTATTTATTTTTTTGAGATGGAGTCT TTTTTATTTA T SPECC1 Ensembl:ENSG00000128487 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1451940819 Functional Loss DEL dbSNP153 25..33 33 - - - Human_RBP_ID_6660904 RMVar_hsa_circ_114616,RMVar_hsa_circ_182679,RMVar_hsa_circ_182682,RMVar_hsa_circ_110443,RMVar_hsa_circ_120355,RMVar_hsa_circ_182683 6591 RMVar_ID_6591 Human_SNP_ID_619665921 A-to-I Human chr17 + 20116081 20116081 20116081 TAGACTATAATATATCAATAACTTTCTTTTTTATTTATTTTATTTATTTATTTTTTTGAGATGGA TAGACTATAATATATCAATAACTTTCTTTTTTGTTTATTTTATTTATTTATTTTTTTGAGATGGA A G SPECC1 Ensembl:ENSG00000128487 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1245886485 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6660904 RMVar_hsa_circ_114616,RMVar_hsa_circ_182679,RMVar_hsa_circ_182682,RMVar_hsa_circ_110443,RMVar_hsa_circ_120355,RMVar_hsa_circ_182683 6592 RMVar_ID_6592 Human_SNP_ID_619677226 A-to-I Human chr17 + 20161934 20161934 20161934 CTCCTGCCTCAGCCTCTTGAGTACCTGGGACTACAGGTGCGTGCCACCATGCCTGGCTAATTTTT CTCCTGCCTCAGCCTCTTGAGTACCTGGGACTGCAGGTGCGTGCCACCATGCCTGGCTAATTTTT A G SPECC1 Ensembl:ENSG00000128487 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs775662841 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114616,RMVar_hsa_circ_182679,RMVar_hsa_circ_182682,RMVar_hsa_circ_110443,RMVar_hsa_circ_120355,RMVar_hsa_circ_182683 6593 RMVar_ID_6593 Human_SNP_ID_619677343 A-to-I Human chr17 + 20162353 20162353 20162353 ATTTTTTAGTAGACACAGGGTTTCACCGCGTTAGCCAGGCTGGTCTCCATCTCCTGACATTGTGA ATTTTTTAGTAGACACAGGGTTTCACCGCGTTGGCCAGGCTGGTCTCCATCTCCTGACATTGTGA A G SPECC1 Ensembl:ENSG00000128487 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1164889439 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114616,RMVar_hsa_circ_182679,RMVar_hsa_circ_182682,RMVar_hsa_circ_110443,RMVar_hsa_circ_120355,RMVar_hsa_circ_182683 6594 RMVar_ID_6594 Human_SNP_ID_619695883 A-to-I Human chr17 + 20233571 20233571 20233571 TTTAGTTATTTATTTTTAGAGATGGGGGTCTCACTATGTTGCCCAGGCTGGACTCGAACTACTGA TTTAGTTATTTATTTTTAGAGATGGGGGTCTCCCTATGTTGCCCAGGCTGGACTCGAACTACTGA A C SPECC1,AC004702.1 Ensembl:ENSG00000128487,Ensembl:ENSG00000263494 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1386802308 Functional Loss SNV dbSNP153 33..33 33 - - - 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_302130,RMVar_hsa_circ_182688,RMVar_hsa_circ_11564,RMVar_hsa_circ_305730,RMVar_hsa_circ_371077,RMVar_hsa_circ_182691,RMVar_hsa_circ_182694,RMVar_hsa_circ_99026 6595 RMVar_ID_6595 Human_SNP_ID_619703661 A-to-I Human chr17 + 20263236 20263236 20263236 GAAGCCATAAGAACCAATAGCTATGACTTCTTATTCTTTCCTGTGTCCTTGGCAGCGTGACTGAT GAAGCCATAAGAACCAATAGCTATGACTTCTTCTTCTTTCCTGTGTCCTTGGCAGCGTGACTGAT A C SPECC1,AC004702.1 Ensembl:ENSG00000128487,Ensembl:ENSG00000263494 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1458122537 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12848,RMVar_hsa_circ_114616,RMVar_hsa_circ_182679,RMVar_hsa_circ_120355,RMVar_hsa_circ_182683,RMVar_hsa_circ_371077,RMVar_hsa_circ_182691,RMVar_hsa_circ_119982,RMVar_hsa_circ_284769,RMVar_hsa_circ_318903,RMVar_hsa_circ_182698,RMVar_hsa_circ_182700,RMVar_hsa_circ_182699,RMVar_hsa_circ_316249,RMVar_hsa_circ_182702,RMVar_hsa_circ_316420 6596 RMVar_ID_6596 Human_SNP_ID_619707387 A-to-I Human chr17 + 20277884 20277884 20277884 TTTCACTCAGCACAGCGTCCTCAGGCCCACTTATGTTGTGGCGTGTGTCAGCCACGCTGCTTCTG TTTCACTCAGCACAGCGTCCTCAGGCCCACTTTTGTTGTGGCGTGTGTCAGCCACGCTGCTTCTG A T SPECC1,AC004702.1 Ensembl:ENSG00000128487,Ensembl:ENSG00000263494 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985870733 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12848,RMVar_hsa_circ_114616,RMVar_hsa_circ_182679,RMVar_hsa_circ_120355,RMVar_hsa_circ_182683,RMVar_hsa_circ_371077,RMVar_hsa_circ_182691,RMVar_hsa_circ_119982,RMVar_hsa_circ_284769,RMVar_hsa_circ_318903,RMVar_hsa_circ_182698,RMVar_hsa_circ_182700,RMVar_hsa_circ_182699,RMVar_hsa_circ_316249,RMVar_hsa_circ_182702,RMVar_hsa_circ_316420 6597 RMVar_ID_6597 Human_SNP_ID_619708633 A-to-I Human chr17 + 20282983 20282983 20282983 GGAGGATTGCTTGACCTCGGGAGTTCAAGACCAGCCTGGGCAACATAGTGAGACCCCATCTCTAA GGAGGATTGCTTGACCTCGGGAGTTCAAGACCGGCCTGGGCAACATAGTGAGACCCCATCTCTAA A G SPECC1,AC004702.1 Ensembl:ENSG00000128487,Ensembl:ENSG00000263494 Protein coding,lincRNA intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1486935789 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12848,RMVar_hsa_circ_114616,RMVar_hsa_circ_182679,RMVar_hsa_circ_120355,RMVar_hsa_circ_182683,RMVar_hsa_circ_371077,RMVar_hsa_circ_182691,RMVar_hsa_circ_119982,RMVar_hsa_circ_284769,RMVar_hsa_circ_318903,RMVar_hsa_circ_182698,RMVar_hsa_circ_182700,RMVar_hsa_circ_182699,RMVar_hsa_circ_316249,RMVar_hsa_circ_182702,RMVar_hsa_circ_316420 6598 RMVar_ID_6598 Human_SNP_ID_619714073 A-to-I Human chr17 + 20302666 20302666 20302666 TCAAGGGATCCTCCCACCTCAGGCTTCAGAGTAGCTGGGATTACAGGCATGTTGCCACCACGTCT TCAAGGGATCCTCCCACCTCAGGCTTCAGAGTGGCTGGGATTACAGGCATGTTGCCACCACGTCT A G SPECC1,AC004702.1 Ensembl:ENSG00000128487,Ensembl:ENSG00000263494 Protein coding,lincRNA intron,intron GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 29129909,30559470 RNA-Seq:(High) rs1014309394 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120355,RMVar_hsa_circ_182683,RMVar_hsa_circ_371077,RMVar_hsa_circ_182691,RMVar_hsa_circ_119982,RMVar_hsa_circ_284769,RMVar_hsa_circ_182700,RMVar_hsa_circ_182699,RMVar_hsa_circ_316249,RMVar_hsa_circ_182702,RMVar_hsa_circ_316420,RMVar_hsa_circ_182705,RMVar_hsa_circ_279784 6599 RMVar_ID_6599 Human_SNP_ID_619714543 A-to-I Human chr17 + 20304222 20304222 20304222 TGAGAAACGAGAATCACTTGGACCTGGGAGGCAGAGGTTGCAGTGAGCTGAGCTCAAGCCACTAC TGAGAAACGAGAATCACTTGGACCTGGGAGGCTGAGGTTGCAGTGAGCTGAGCTCAAGCCACTAC A T SPECC1,AC004702.1 Ensembl:ENSG00000128487,Ensembl:ENSG00000263494 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs907393909 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120355,RMVar_hsa_circ_182683,RMVar_hsa_circ_371077,RMVar_hsa_circ_182691,RMVar_hsa_circ_119982,RMVar_hsa_circ_284769,RMVar_hsa_circ_182700,RMVar_hsa_circ_182699,RMVar_hsa_circ_316249,RMVar_hsa_circ_182702,RMVar_hsa_circ_316420,RMVar_hsa_circ_182705,RMVar_hsa_circ_279784 6600 RMVar_ID_6600 Human_SNP_ID_619717100 A-to-I Human chr17 + 20314519 20314518 20314519 GCCCTTGGCTGGGTGTGGTAGCTCGTGGCTGTAATCCCAGCACTTTAGGAAGCCAAGGCAGTAGG GCCCTTGGCTGGGTGTGGTAGCTCGTGGCTGT_ATCCCAGCACTTTAGGAAGCCAAGGCAGTAGG TA T SPECC1,AC004702.1 Ensembl:ENSG00000128487,Ensembl:ENSG00000263494 Protein coding,lincRNA 3'UTR,intron GSE100210;GSE107867 HepG2 cell line;ASD brains,frontal_cortex - 29129909,30559470 RNA-Seq:(High) rs555831289 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_484892 Human_miRNA_ID_1943261,Human_miRNA_ID_1946306,Human_miRNA_ID_2117452,Human_miRNA_ID_2201034,Human_miRNA_ID_2204097,Human_miRNA_ID_2316638,Human_miRNA_ID_2319794,Human_miRNA_ID_2322950,Human_miRNA_ID_2326123,Human_miRNA_ID_2329222,Human_miRNA_ID_2520500,Human_miRNA_ID_2523663,Human_miRNA_ID_2775502,Human_miRNA_ID_2816555,Human_miRNA_ID_2822852,Human_miRNA_ID_2828986,Human_miRNA_ID_2832144,Human_miRNA_ID_2836264,Human_miRNA_ID_2841619,Human_miRNA_ID_2863818,Human_miRNA_ID_3113551 RMVar_hsa_circ_119982,RMVar_hsa_circ_182700,RMVar_hsa_circ_122205,RMVar_hsa_circ_182706 6601 RMVar_ID_6601 Human_SNP_ID_619717128 A-to-I Human chr17 + 20314621 20314618 20314622 ATGAGCATACCACTGCACTCCAGCCTGTGTGAAAGAGCCAGACCCTGTCTCAAAAAAATGATAAA ATGAGCATACCACTGCACTCCAGCCTGTGT____GAGCCAGACCCTGTCTCAAAAAAATGATAAA TGAAA T SPECC1,AC004702.1 Ensembl:ENSG00000128487,Ensembl:ENSG00000263494 Protein coding,lincRNA 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900623009 Functional Loss DEL dbSNP153 31..34 33 - - - RMVar_hsa_circ_119982,RMVar_hsa_circ_182700,RMVar_hsa_circ_122205,RMVar_hsa_circ_182706 6602 RMVar_ID_6602 Human_SNP_ID_619717675 A-to-I Human chr17 + 20316471 20316471 20316471 TCACTGCAACCTCCGCCGCCCGTGTTTAAGCGATTCTCCTGCCTCAGCCTCCCATGTGGCTGGGA TCACTGCAACCTCCGCCGCCCGTGTTTAAGCGTTTCTCCTGCCTCAGCCTCCCATGTGGCTGGGA A T SPECC1,AC004702.1 Ensembl:ENSG00000128487,Ensembl:ENSG00000263494 Protein coding,lincRNA 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1393638369 Functional Loss SNV dbSNP153 33..33 33 - - - 6603 RMVar_ID_6603 Human_SNP_ID_619718076 A-to-I Human chr17 + 20317686 20317686 20317686 AGTTTGAGGCTGCAGTAAGCTGTGTTTGTGCCACTGCACTCTGGCCTGGGCCAAAGAGCAAGACC AGTTTGAGGCTGCAGTAAGCTGTGTTTGTGCCTCTGCACTCTGGCCTGGGCCAAAGAGCAAGACC A T SPECC1,AC004702.1 Ensembl:ENSG00000128487,Ensembl:ENSG00000263494 Protein coding,lincRNA 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1359247015 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6568819,Human_RBP_ID_12924076 6604 RMVar_ID_6604 Human_SNP_ID_619720826 A-to-I Human chr17 + 20327713 20327713 20327713 GAAAAATTAGCTGGACATGGTGGAGCGTGCCTATGGTCCCAGCTACTCAGGAGGCTGAGGCAGGA GAAAAATTAGCTGGACATGGTGGAGCGTGCCTGTGGTCCCAGCTACTCAGGAGGCTGAGGCAGGA A G CCDC144CP Ensembl:ENSG00000154898 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270436163 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17378883 RMVar_hsa_circ_15662 6605 RMVar_ID_6605 Human_SNP_ID_619787133 A-to-I Human chr17 - 20612915 20612915 20612915 GCTCCAGAATCACCTGCTTGCACTCCTCGATCACCTGCCGCAGCACAGGGCGGGAGAAGTGGTCC GCTCCAGAATCACCTGCTTGCACTCCTCGATCCCCTGCCGCAGCACAGGGCGGGAGAAGTGGTCC T G LINC02088 Ensembl:ENSG00000227685 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs963786058 Functional Loss SNV dbSNP153 33..33 33 - - - 6606 RMVar_ID_6606 Human_SNP_ID_619787403 A-to-I Human chr17 + 20613892 20613892 20613892 ACAGCCACACGTCTGTATGCACCGACTGCTCCACCGTCTTCCACAGGGACTGCTACTACGACAAC ACAGCCACACGTCTGTATGCACCGACTGCTCCGCCGTCTTCCACAGGGACTGCTACTACGACAAC A G AC087499.4 Ensembl:ENSG00000235546 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417331078 Functional Loss SNV dbSNP153 33..33 33 - - - 6607 RMVar_ID_6607 Human_SNP_ID_619889339 A-to-I Human chr17 - 21000779 21000773 21000779 GGATTATAGGCGTGAGCCACCGCACCTGGCCTATGAGTGGTCTTTTAATTAGGAACAAATCTAAT GGATTATAGGCGTGAGCCACCGCACCTGGCCT______GGTCTTTTAATTAGGAACAAATCTAAT CACTCAT C USP22 Ensembl:ENSG00000124422 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1445863355 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_484965,Human_RBP_ID_1850939,Human_RBP_ID_3515077,Human_RBP_ID_6569045,Human_RBP_ID_8190924,Human_RBP_ID_8446595,Human_RBP_ID_8814160,Human_RBP_ID_12925011,Human_RBP_ID_17263864,Human_RBP_ID_23715867,Human_RBP_ID_26447912,Human_RBP_ID_27662400 Human_miRNA_ID_192480,Human_miRNA_ID_1135865,Human_miRNA_ID_1138378 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 6608 RMVar_ID_6608 Human_SNP_ID_619889340 A-to-I Human chr17 - 21000779 21000779 21000779 GGATTATAGGCGTGAGCCACCGCACCTGGCCTATGAGTGGTCTTTTAATTAGGAACAAATCTAAT GGATTATAGGCGTGAGCCACCGCACCTGGCCTGTGAGTGGTCTTTTAATTAGGAACAAATCTAAT T C USP22 Ensembl:ENSG00000124422 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1337708460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_484965,Human_RBP_ID_1850939,Human_RBP_ID_3515077,Human_RBP_ID_6569045,Human_RBP_ID_8190924,Human_RBP_ID_8446595,Human_RBP_ID_8814160,Human_RBP_ID_12925011,Human_RBP_ID_17263864,Human_RBP_ID_23715867,Human_RBP_ID_26447912,Human_RBP_ID_27662400 Human_miRNA_ID_192480,Human_miRNA_ID_1135865,Human_miRNA_ID_1138378 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 6609 RMVar_ID_6609 Human_SNP_ID_619890861 A-to-I Human chr17 - 21005549 21005549 21005549 ACTGAGGGAGGTGACAGTACTGTTCTAAGGTCAGGGTCTCAAAGATCTTGGTGTTTCCTGCCAAA ACTGAGGGAGGTGACAGTACTGTTCTAAGGTCGGGGTCTCAAAGATCTTGGTGTTTCCTGCCAAA T C USP22 Ensembl:ENSG00000124422 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs572117640 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12925205 RMVar_hsa_circ_26559,RMVar_hsa_circ_182717,RMVar_hsa_circ_84782,RMVar_hsa_circ_104605,RMVar_hsa_circ_182719,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_110332,RMVar_hsa_circ_125521,RMVar_hsa_circ_108933,RMVar_hsa_circ_51758,RMVar_hsa_circ_182724,RMVar_hsa_circ_182726,RMVar_hsa_circ_182727,RMVar_hsa_circ_182725,RMVar_hsa_circ_182723,RMVar_hsa_circ_372154,RMVar_hsa_circ_182729 6610 RMVar_ID_6610 Human_SNP_ID_619898713 A-to-I Human chr17 - 21032782 21032782 21032782 GGTGTGTGCCACCATGCCCAGCTAATTTTTGCATTTTTTGTAGAGATGAGGTTTCACCATTTGGC GGTGTGTGCCACCATGCCCAGCTAATTTTTGCTTTTTTTGTAGAGATGAGGTTTCACCATTTGGC T A USP22 Ensembl:ENSG00000124422 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs113698492 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12926495 RMVar_hsa_circ_124521,RMVar_hsa_circ_182749 6611 RMVar_ID_6611 Human_SNP_ID_619898714 A-to-I Human chr17 - 21032782 21032782 21032782 GGTGTGTGCCACCATGCCCAGCTAATTTTTGCATTTTTTGTAGAGATGAGGTTTCACCATTTGGC GGTGTGTGCCACCATGCCCAGCTAATTTTTGCGTTTTTTGTAGAGATGAGGTTTCACCATTTGGC T C USP22 Ensembl:ENSG00000124422 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs113698492 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12926495 RMVar_hsa_circ_124521,RMVar_hsa_circ_182749 6612 RMVar_ID_6612 Human_SNP_ID_619899082 A-to-I Human chr17 - 21033923 21033923 21033923 CCAACATGGTGAAACCTCATCTGTACTAAAATACAAAAAGTTAGCCGAGCATGGTGGCACGCGCC CCAACATGGTGAAACCTCATCTGTACTAAAATGCAAAAAGTTAGCCGAGCATGGTGGCACGCGCC T C USP22 Ensembl:ENSG00000124422 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs915493054 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12926542,Human_RBP_ID_25257357 RMVar_hsa_circ_124521,RMVar_hsa_circ_182749 6613 RMVar_ID_6613 Human_SNP_ID_619900619 A-to-I Human chr17 - 21039100 21039100 21039100 AAAAATACACAAAATTAGCTGGGCATGGTGGCACGCGCCTGTAATCCCAGCTACTCGTGAGGCTG AAAAATACACAAAATTAGCTGGGCATGGTGGCTCGCGCCTGTAATCCCAGCTACTCGTGAGGCTG T A USP22 Ensembl:ENSG00000124422 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1456218082 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124521,RMVar_hsa_circ_182749 6614 RMVar_ID_6614 Human_SNP_ID_619900695 A-to-I Human chr17 - 21039334 21039334 21039334 ACCTCAGGTGATCCGCCCATCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCGC ACCTCAGGTGATCCGCCCATCTTGGCCTCCCATAGTGCTGGGATTACAGGCATGAGCCACCGCGC T A USP22 Ensembl:ENSG00000124422 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs557053914 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25257422 RMVar_hsa_circ_124521,RMVar_hsa_circ_182749 6615 RMVar_ID_6615 Human_SNP_ID_619900760 A-to-I Human chr17 - 21039525 21039525 21039525 GTTTTCACTCTTTTTGCCCAGGCTGGAGGGCAATGGCGTGATCTCGGCTCACCACAGCCTCCCCC GTTTTCACTCTTTTTGCCCAGGCTGGAGGGCAGTGGCGTGATCTCGGCTCACCACAGCCTCCCCC T C USP22 Ensembl:ENSG00000124422 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs547170701 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124521,RMVar_hsa_circ_182749 6616 RMVar_ID_6616 Human_SNP_ID_619901237 A-to-I Human chr17 - 21041038 21041038 21041038 TCTACTAAAAATACGAAAAGTAGCCGGGTGTGATGGCGGGCGCCTGTAATCCCAGCTACTCCAGA TCTACTAAAAATACGAAAAGTAGCCGGGTGTGTTGGCGGGCGCCTGTAATCCCAGCTACTCCAGA T A USP22 Ensembl:ENSG00000124422 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1301803270 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124521,RMVar_hsa_circ_182749 6617 RMVar_ID_6617 Human_SNP_ID_619901425 A-to-I Human chr17 - 21041538 21041538 21041538 GCTGGAGTGCAGTGGCGCGATTTCGGCTCACTACAATCTCCGCCTCCCGGGTTCAGCCGATTCTC GCTGGAGTGCAGTGGCGCGATTTCGGCTCACTGCAATCTCCGCCTCCCGGGTTCAGCCGATTCTC T C USP22 Ensembl:ENSG00000124422 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1313237183 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12926898 RMVar_hsa_circ_124521,RMVar_hsa_circ_182749 6618 RMVar_ID_6618 Human_SNP_ID_619926099 A-to-I Human chr17 + 21137984 21137984 21137984 TCGATCTCCCGACCTCGTGATCTGCTTGCCTCAGCCTCCCATAGTTCTGGGATTACATATTTCTG TCGATCTCCCGACCTCGTGATCTGCTTGCCTCGGCCTCCCATAGTTCTGGGATTACATATTTCTG A G DHRS7B Ensembl:ENSG00000109016 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006912793 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86338,RMVar_hsa_circ_99774,RMVar_hsa_circ_182758,RMVar_hsa_circ_182759 6619 RMVar_ID_6619 Human_SNP_ID_619931459 A-to-I Human chr17 + 21159609 21159609 21159609 TAAAGGACTGTTATCAGTTGGAATGGTGGCTGATGTCTATAATCCCAGCACTTTGGGAGGCCAAG TAAAGGACTGTTATCAGTTGGAATGGTGGCTGTTGTCTATAATCCCAGCACTTTGGGAGGCCAAG A T DHRS7B Ensembl:ENSG00000109016 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1268244223 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86338,RMVar_hsa_circ_99774,RMVar_hsa_circ_182758,RMVar_hsa_circ_182759 6620 RMVar_ID_6620 Human_SNP_ID_619931461 A-to-I Human chr17 + 21159615 21159615 21159615 ACTGTTATCAGTTGGAATGGTGGCTGATGTCTATAATCCCAGCACTTTGGGAGGCCAAGATGAGA ACTGTTATCAGTTGGAATGGTGGCTGATGTCTGTAATCCCAGCACTTTGGGAGGCCAAGATGAGA A G DHRS7B Ensembl:ENSG00000109016 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs943036848 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86338,RMVar_hsa_circ_99774,RMVar_hsa_circ_182758,RMVar_hsa_circ_182759 6621 RMVar_ID_6621 Human_SNP_ID_619931499 A-to-I Human chr17 + 21159751 21159751 21159751 TTAAAGTTAGCTAGTCACAGTGGTGTGTGCCTATAGTCCTAGCTACTTGGGAAGCTGAGGCAGGA TTAAAGTTAGCTAGTCACAGTGGTGTGTGCCTGTAGTCCTAGCTACTTGGGAAGCTGAGGCAGGA A G DHRS7B Ensembl:ENSG00000109016 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1257488395 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86338,RMVar_hsa_circ_99774,RMVar_hsa_circ_182758,RMVar_hsa_circ_182759 6622 RMVar_ID_6622 Human_SNP_ID_619932823 A-to-I Human chr17 + 21165822 21165822 21165822 CCTGTAGTCGCAGCTACGCGGGAGGCTGAGGCAGAAGAATTACTTGAACCCAGGAGGTGGAGGTT CCTGTAGTCGCAGCTACGCGGGAGGCTGAGGCTGAAGAATTACTTGAACCCAGGAGGTGGAGGTT A T DHRS7B Ensembl:ENSG00000109016 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1275910029 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86338,RMVar_hsa_circ_99774,RMVar_hsa_circ_182758,RMVar_hsa_circ_182759 6623 RMVar_ID_6623 Human_SNP_ID_619935068 A-to-I Human chr17 + 21175786 21175786 21175786 ATGGCGAAACCTCATCTCTACAAAAGTTAGCCAAGCATGGTGGCATGTGCCTGTAGTCCCGGCAA ATGGCGAAACCTCATCTCTACAAAAGTTAGCCGAGCATGGTGGCATGTGCCTGTAGTCCCGGCAA A G DHRS7B Ensembl:ENSG00000109016 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1002864164 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2367,RMVar_hsa_circ_86338,RMVar_hsa_circ_99774,RMVar_hsa_circ_182758,RMVar_hsa_circ_182759,RMVar_hsa_circ_90331,RMVar_hsa_circ_182760 6624 RMVar_ID_6624 Human_SNP_ID_619939671 A-to-I Human chr17 - 21195732 21195732 21195732 TTGAAGGCTGAGTGCAGTAGCTCATGCCTGTAATCCCAGCACGTTGGGAGGCTGAGGCAGGAGGA TTGAAGGCTGAGTGCAGTAGCTCATGCCTGTAGTCCCAGCACGTTGGGAGGCTGAGGCAGGAGGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1398286184 Functional Loss SNV dbSNP153 33..33 33 - - - 6625 RMVar_ID_6625 Human_SNP_ID_619942934 A-to-I Human chr17 - 21208281 21208281 21208281 CCTGTTATAAAAGAAACACTTTGGCCGGGCGCAGTGGCTCATGCCTGTAATCCCAACACTTTGGG CCTGTTATAAAAGAAACACTTTGGCCGGGCGCGGTGGCTCATGCCTGTAATCCCAACACTTTGGG T C TMEM11 Ensembl:ENSG00000178307 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1225547503 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108723,RMVar_hsa_circ_182766 6626 RMVar_ID_6626 Human_SNP_ID_619956629 A-to-I Human chr17 - 21260016 21260016 21260016 GTGACCAACACAAGAACATATGCCAGTTCCTCATAGAGACTGGACTGGCTAAGGACGATCAGCTG GTGACCAACACAAGAACATATGCCAGTTCCTCGTAGAGACTGGACTGGCTAAGGACGATCAGCTG T C EIF1P5 Ensembl:ENSG00000266563 Pseudogene exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs879205433 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1877007 6627 RMVar_ID_6627 Human_SNP_ID_619956632 A-to-I Human chr17 - 21260039 21260039 21260039 TGGAGAAGTACTTCAGCTATAGGGTGACCAACACAAGAACATATGCCAGTTCCTCATAGAGACTG TGGAGAAGTACTTCAGCTATAGGGTGACCAACGCAAGAACATATGCCAGTTCCTCATAGAGACTG T C EIF1P5 Ensembl:ENSG00000266563 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878871212 Functional Loss SNV dbSNP153 33..33 33 - - - 6628 RMVar_ID_6628 Human_SNP_ID_619965195 A-to-I Human chr17 + 21292554 21292554 21292554 CATTTTTGTTTTGTTTTATTTTTTGTAGAGACAGGATTTTGTCATGTTGCCCAGGCTAGTATTGA CATTTTTGTTTTGTTTTATTTTTTGTAGAGACGGGATTTTGTCATGTTGCCCAGGCTAGTATTGA A G MAP2K3 Ensembl:ENSG00000034152 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1252798021 Functional Loss SNV dbSNP153 33..33 33 - - - 6629 RMVar_ID_6629 Human_SNP_ID_620035084 A-to-I Human chr17 - 21543243 21543243 21543243 TGTCCTGGTGGTAGTGAGTGAGTTCTTGCTCTATGGAACATGAGAGCTGGTTGTTGTGAAAGCGC TGTCCTGGTGGTAGTGAGTGAGTTCTTGCTCTGTGGAACATGAGAGCTGGTTGTTGTGAAAGCGC T C LINC02693 Ensembl:ENSG00000212719 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1272976004 Functional Loss SNV dbSNP153 33..33 33 - - - 6630 RMVar_ID_6630 Human_SNP_ID_620799100 A-to-I Human chr17 + 27083529 27083529 27083529 CACATACACCACCACATGCTCCACCCCAATCTATTTGGCCAGTAATAAGTGCTCTCGGGTCTAGG CACATACACCACCACATGCTCCACCCCAATCTGTTTGGCCAGTAATAAGTGCTCTCGGGTCTAGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878876452 Functional Loss SNV dbSNP153 33..33 33 - - - 6631 RMVar_ID_6631 Human_SNP_ID_620799114 A-to-I Human chr17 + 27083559 27083559 27083559 CTATTTGGCCAGTAATAAGTGCTCTCGGGTCTAGGGCATGGGGCTGTCATTGGCTGCTACCACCA CTATTTGGCCAGTAATAAGTGCTCTCGGGTCTGGGGCATGGGGCTGTCATTGGCTGCTACCACCA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879186451 Functional Loss SNV dbSNP153 33..33 33 - - - 6632 RMVar_ID_6632 Human_SNP_ID_620860731 A-to-I Human chr17 + 27297305 27297305 27297305 CTCCTGCCTCACCCTCCCGAGTAGCTGGGATTACAGGTTCGTGCCACCACACCTGGCTGATTTTT CTCCTGCCTCACCCTCCCGAGTAGCTGGGATTGCAGGTTCGTGCCACCACACCTGGCTGATTTTT A G WSB1 Ensembl:ENSG00000109046 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1046626987 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1793853 6633 RMVar_ID_6633 Human_SNP_ID_620861073 A-to-I Human chr17 + 27298483 27298483 27298483 GTGGGTCATGCCTTAATCTCACCGCTTTGGGAAACCAAGGTGGGAGGATCGTTTGAGGCCAGGAG GTGGGTCATGCCTTAATCTCACCGCTTTGGGACACCAAGGTGGGAGGATCGTTTGAGGCCAGGAG A C WSB1 Ensembl:ENSG00000109046 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1162480046 Functional Loss SNV dbSNP153 33..33 33 - - - 6634 RMVar_ID_6634 Human_SNP_ID_620863832 A-to-I Human chr17 + 27309152 27309152 27309152 TAAATACACCATGATACGGAAACTAGAAGGACATCACCATGATGTGGTAGCTTGTGACTTTTCTC TAAATACACCATGATACGGAAACTAGAAGGACTTCACCATGATGTGGTAGCTTGTGACTTTTCTC A T WSB1 Ensembl:ENSG00000109046 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1316396735 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_896302,Human_RBP_ID_1529718,Human_RBP_ID_1851484,Human_RBP_ID_6571387,Human_RBP_ID_8089114,Human_RBP_ID_9346183,Human_RBP_ID_9377706,Human_RBP_ID_12934270,Human_RBP_ID_17887480,Human_RBP_ID_18438548,Human_RBP_ID_18470004,Human_RBP_ID_18988053,Human_RBP_ID_22061115,Human_RBP_ID_22655971,Human_RBP_ID_22948049,Human_RBP_ID_23114241,Human_RBP_ID_25335381,Human_RBP_ID_26334050,Human_RBP_ID_27662633,Human_RBP_ID_27812389 Human_Splice_Rec_1793918,Human_Splice_Rec_1793932,Human_Splice_Rec_1793950,Human_Splice_Rec_1793962 Human_miRNA_ID_2277093 RMVar_hsa_circ_119708,RMVar_hsa_circ_21029,RMVar_hsa_circ_371789,RMVar_hsa_circ_309793,RMVar_hsa_circ_182771,RMVar_hsa_circ_182772,RMVar_hsa_circ_182776,RMVar_hsa_circ_280009,RMVar_hsa_circ_285337,RMVar_hsa_circ_182774,RMVar_hsa_circ_281906,RMVar_hsa_circ_182777,RMVar_hsa_circ_108747,RMVar_hsa_circ_273217,RMVar_hsa_circ_320257,RMVar_hsa_circ_182775,RMVar_hsa_circ_273238,RMVar_hsa_circ_182783,RMVar_hsa_circ_182784,RMVar_hsa_circ_182782,RMVar_hsa_circ_182785,RMVar_hsa_circ_182786 6635 RMVar_ID_6635 Human_SNP_ID_620864853 A-to-I Human chr17 + 27312807 27312807 27312807 GACTTACGAAAGTTGAATTGGGTGAGGCGGGCAAATCACCTGAGGTCAGCAGTTTGAGACTAGCC GACTTACGAAAGTTGAATTGGGTGAGGCGGGCGAATCACCTGAGGTCAGCAGTTTGAGACTAGCC A G WSB1 Ensembl:ENSG00000109046 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs11550665 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_485372,Human_RBP_ID_768342,Human_RBP_ID_25258899 6636 RMVar_ID_6636 Human_SNP_ID_620864897 A-to-I Human chr17 + 27312985 27312985 27312985 ATTGCTTGAACCCAGGAGGTGGAGGTTGCAGTAAGCCAAGATCACACCACTGCACTCCAACCTGG ATTGCTTGAACCCAGGAGGTGGAGGTTGCAGTGAGCCAAGATCACACCACTGCACTCCAACCTGG A G WSB1 Ensembl:ENSG00000109046 Protein coding exon GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs878966575 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26448153 6637 RMVar_ID_6637 Human_SNP_ID_620865286 A-to-I Human chr17 + 27314482 27314482 27314482 CCTGTACTCCTAGCTACTTAGGAGGCTGAGGCAAGAGAATTGCTTGAACTGGAGAAATGGAGGTT CCTGTACTCCTAGCTACTTAGGAGGCTGAGGCGAGAGAATTGCTTGAACTGGAGAAATGGAGGTT A G WSB1 Ensembl:ENSG00000109046 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1221685409 Functional Loss SNV dbSNP153 33..33 33 - - - 6638 RMVar_ID_6638 Human_SNP_ID_620870316 A-to-I Human chr17 + 27337045 27337045 27337045 CCAGCTACTGGGGACGCTGAGGCAGGAGGATCACTTGAGCCCAGGAGGTTGACGCTCAGTGAACT CCAGCTACTGGGGACGCTGAGGCAGGAGGATCGCTTGAGCCCAGGAGGTTGACGCTCAGTGAACT A G AC026254.2 Ensembl:ENSG00000266313 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs961232354 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18691941 6639 RMVar_ID_6639 Human_SNP_ID_620902598 A-to-I Human chr17 + 27472976 27472966 27472977 CAGTGTTTCCTAGGCTGGAGTTCCATGGCACCATCATGGCTCACTGCAGCCTCTGTCTACCTCTC CAGTGTTTCCTAGGCTGGAGTTC___________CATGGCTCACTGCAGCCTCTGTCTACCTCTC CCATGGCACCAT C KSR1 Ensembl:ENSG00000141068 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1209389291 Functional Loss DEL dbSNP153 24..34 33 - - - Human_RBP_ID_17565528 6640 RMVar_ID_6640 Human_SNP_ID_620934196 A-to-I Human chr17 + 27606030 27606030 27606030 GGGCTGGTGCAGTGGCCCATGTCTGTAATCCCAACACTTTGGGAGGCCAAGGTGGAAGGATTGCT GGGCTGGTGCAGTGGCCCATGTCTGTAATCCCCACACTTTGGGAGGCCAAGGTGGAAGGATTGCT A C KSR1 Ensembl:ENSG00000141068 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1166742969 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118334,RMVar_hsa_circ_182793,RMVar_hsa_circ_345352,RMVar_hsa_circ_50008,RMVar_hsa_circ_87288,RMVar_hsa_circ_182797,RMVar_hsa_circ_378818 6641 RMVar_ID_6641 Human_SNP_ID_621046117 A-to-I Human chr17 + 28050921 28050920 28050922 CAGCCCAAGAGTTCGAGACCAGCCTGGACAACATAGTGAAATCTCATCTCCACTAAAAGTACAGA CAGCCCAAGAGTTCGAGACCAGCCTGGACAAC__AGTGAAATCTCATCTCCACTAAAAGTACAGA CAT C NLK Ensembl:ENSG00000087095 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1434742827 Functional Loss DEL dbSNP153 33..34 33 - - - 6642 RMVar_ID_6642 Human_SNP_ID_621049043 A-to-I Human chr17 + 28063152 28063151 28063152 TGGGGTTTTGTTATGTTGTCCAGGCTGTTCTCAAACTCTTGGGATCAAGCTCTCCGCCCACTTTG TGGGGTTTTGTTATGTTGTCCAGGCTGTTCTC_AACTCTTGGGATCAAGCTCTCCGCCCACTTTG CA C NLK Ensembl:ENSG00000087095 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1252618071 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_12936182 6643 RMVar_ID_6643 Human_SNP_ID_621050624 A-to-I Human chr17 + 28070193 28070193 28070193 AGGAGGCGGAGGTTGCAGTGAGCCAAGATCGCACCACCGCGCTCCAGCCTGGGCAACAGAGCAAG AGGAGGCGGAGGTTGCAGTGAGCCAAGATCGCGCCACCGCGCTCCAGCCTGGGCAACAGAGCAAG A G NLK Ensembl:ENSG00000087095 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1477935100 Functional Loss SNV dbSNP153 33..33 33 - - - 6644 RMVar_ID_6644 Human_SNP_ID_621054053 A-to-I Human chr17 + 28085673 28085673 28085673 TGAGACAGGAGAACCGCTTGAACCCAGGAGGCAGAGGCTGCAGTGAGCCAAGATGGTGCCACTGC TGAGACAGGAGAACCGCTTGAACCCAGGAGGCGGAGGCTGCAGTGAGCCAAGATGGTGCCACTGC A G NLK Ensembl:ENSG00000087095 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1297748395 Functional Loss SNV dbSNP153 33..33 33 - - - 6645 RMVar_ID_6645 Human_SNP_ID_621058023 A-to-I Human chr17 + 28104395 28104395 28104395 CTCCTTCCTTAGCCTCCTGAGTAGCTGGGATTACAGGCACACGCCACTATGCCCAGCTAATTTTT CTCCTTCCTTAGCCTCCTGAGTAGCTGGGATTGCAGGCACACGCCACTATGCCCAGCTAATTTTT A G NLK Ensembl:ENSG00000087095 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1471183511 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_182806 6646 RMVar_ID_6646 Human_SNP_ID_621079685 A-to-I Human chr17 + 28201458 28201458 28201458 AATCACAGCTTCTCGGGAGGCTGAGGAAGAATAGCTTGAACCCAGGAGGTGGAGGTTGCAGTGAG AATCACAGCTTCTCGGGAGGCTGAGGAAGAATCGCTTGAACCCAGGAGGTGGAGGTTGCAGTGAG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913110905 Functional Loss SNV dbSNP153 33..33 33 - - - 6647 RMVar_ID_6647 Human_SNP_ID_621079686 A-to-I Human chr17 + 28201458 28201458 28201458 AATCACAGCTTCTCGGGAGGCTGAGGAAGAATAGCTTGAACCCAGGAGGTGGAGGTTGCAGTGAG AATCACAGCTTCTCGGGAGGCTGAGGAAGAATTGCTTGAACCCAGGAGGTGGAGGTTGCAGTGAG A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913110905 Functional Loss SNV dbSNP153 33..33 33 - - - 6648 RMVar_ID_6648 Human_SNP_ID_621109411 A-to-I Human chr17 + 28326981 28326981 28326981 CCCTCACCTTCTTCCATTTTTTTTTTTTTTTTAAGACAGTCTCACTCTGTTGCCCAGGCTGGAGT CCCTCACCTTCTTCCATTTTTTTTTTTTTTTTTAGACAGTCTCACTCTGTTGCCCAGGCTGGAGT A T TMEM97 Ensembl:ENSG00000109084 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1061480 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6572588,Human_RBP_ID_12938006,Human_RBP_ID_22803627,Human_RBP_ID_22960296,Human_RBP_ID_24478126,Human_RBP_ID_26448263,Human_RBP_ID_26957383,Human_RBP_ID_27251554,Human_RBP_ID_27450111 6649 RMVar_ID_6649 Human_SNP_ID_621109480 A-to-I Human chr17 + 28327205 28327205 28327205 GTTGCCCAGGTTGGTCTCGAACGCCTAGGCTCAAGTGATCTGCCCACCTCAGTCTCCCTAAGTGC GTTGCCCAGGTTGGTCTCGAACGCCTAGGCTCGAGTGATCTGCCCACCTCAGTCTCCCTAAGTGC A G TMEM97 Ensembl:ENSG00000109084 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1376059830 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_768358,Human_RBP_ID_4412936,Human_RBP_ID_6572600,Human_RBP_ID_8191834,Human_RBP_ID_12938018,Human_RBP_ID_23717572,Human_RBP_ID_26448274 6650 RMVar_ID_6650 Human_SNP_ID_621109854 A-to-I Human chr17 - 28328656 28328656 28328656 AAATGAATTTATTGACCAATTTATTTTTCAGAAATGAACTGAAAATTTCGCTTTTATAGTAGGAA AAATGAATTTATTGACCAATTTATTTTTCAGAGATGAACTGAAAATTTCGCTTTTATAGTAGGAA T C IFT20 Ensembl:ENSG00000109083 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1273691506 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1851813,Human_RBP_ID_5115091,Human_RBP_ID_18289965,Human_RBP_ID_25259652 Human_Splice_Rec_1794936,Human_Splice_Rec_1794946,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 6651 RMVar_ID_6651 Human_SNP_ID_621126179 A-to-I Human chr17 + 28386977 28386977 28386977 CCCAGGCTGTTCTCAAACTCCTGGCCTCAAGCAATCTTCCCAACTTAGCCTCCCAAAGTGTTGAG CCCAGGCTGTTCTCAAACTCCTGGCCTCAAGCCATCTTCCCAACTTAGCCTCCCAAAGTGTTGAG A C SARM1 Ensembl:ENSG00000004139 Protein coding intron GSE47997;GSE38233;GSE38233 K562 cells&HepG2 cells;cultured B-cells;cultured B-cells - 23474544,24183664,24183664 RNA-Seq:(High) rs897306300 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80080,RMVar_hsa_circ_327482,RMVar_hsa_circ_377723,RMVar_hsa_circ_182841 6652 RMVar_ID_6652 Human_SNP_ID_621126731 A-to-I Human chr17 + 28388810 28388810 28388810 TTTTTGTTTTTGAGGTAGAGTCTCGCTCTGTCACTCAGGCTGGAGTGCAATGGCGTGATCTTGGC TTTTTGTTTTTGAGGTAGAGTCTCGCTCTGTCCCTCAGGCTGGAGTGCAATGGCGTGATCTTGGC A C SARM1 Ensembl:ENSG00000004139 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs547013711 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80080,RMVar_hsa_circ_182841 6653 RMVar_ID_6653 Human_SNP_ID_621126774 A-to-I Human chr17 + 28388947 28388947 28388947 TGCCCGCCACCACGGCTGGCTAATTTTTTTGTATTTTTAGTAGAGACAGGGTTTCACCGTGTTAG TGCCCGCCACCACGGCTGGCTAATTTTTTTGTGTTTTTAGTAGAGACAGGGTTTCACCGTGTTAG A G SARM1 Ensembl:ENSG00000004139 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1275147041 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80080,RMVar_hsa_circ_182841 6654 RMVar_ID_6654 Human_SNP_ID_621126931 A-to-I Human chr17 + 28389767 28389767 28389767 AAAATTAGCCAGGCATGGTGGCGCACACCTGTAATCCCAGCTACTCAGGAGACTGAGGCAGGGGA AAAATTAGCCAGGCATGGTGGCGCACACCTGTCATCCCAGCTACTCAGGAGACTGAGGCAGGGGA A C SARM1 Ensembl:ENSG00000004139 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1555586636 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80080,RMVar_hsa_circ_182841 6655 RMVar_ID_6655 Human_SNP_ID_621127498 A-to-I Human chr17 + 28392148 28392148 28392148 TTTTTTTTTTTGAGGCACAGTCTTGCTCTATCACCAGGTTGGAGTGCAGTGGTGAGATCTTGGTC TTTTTTTTTTTGAGGCACAGTCTTGCTCTATCTCCAGGTTGGAGTGCAGTGGTGAGATCTTGGTC A T SARM1 Ensembl:ENSG00000004139 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1263382223 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80080,RMVar_hsa_circ_182841 6656 RMVar_ID_6656 Human_SNP_ID_621127505 A-to-I Human chr17 + 28392191 28392191 28392191 GTGCAGTGGTGAGATCTTGGTCGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGTGATTCCCCT GTGCAGTGGTGAGATCTTGGTCGGCTCACTGCTACCTCCGCCTCCCGGGTTCAAGTGATTCCCCT A T SARM1 Ensembl:ENSG00000004139 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1337969118 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80080,RMVar_hsa_circ_182841 6657 RMVar_ID_6657 Human_SNP_ID_621127518 A-to-I Human chr17 + 28392253 28392253 28392253 CCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCACACGCCACCATATCCAGCTAATTTATAT CCTGCCTCAGCCTCCTGAGTAGCTGGGACTACGGGCACACGCCACCATATCCAGCTAATTTATAT A G SARM1 Ensembl:ENSG00000004139 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs531805631 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80080,RMVar_hsa_circ_182841 6658 RMVar_ID_6658 Human_SNP_ID_621127519 A-to-I Human chr17 + 28392253 28392253 28392253 CCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCACACGCCACCATATCCAGCTAATTTATAT CCTGCCTCAGCCTCCTGAGTAGCTGGGACTACTGGCACACGCCACCATATCCAGCTAATTTATAT A T SARM1 Ensembl:ENSG00000004139 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs531805631 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80080,RMVar_hsa_circ_182841 6659 RMVar_ID_6659 Human_SNP_ID_621127533 A-to-I Human chr17 + 28392301 28392301 28392301 ATCCAGCTAATTTATATATATATATTTTTAGTAGAGACGGGGTTTCACCATCTTGGCCAAGATGG ATCCAGCTAATTTATATATATATATTTTTAGTGGAGACGGGGTTTCACCATCTTGGCCAAGATGG A G SARM1 Ensembl:ENSG00000004139 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1293725891 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80080,RMVar_hsa_circ_182841 6660 RMVar_ID_6660 Human_SNP_ID_621171008 A-to-I Human chr17 - 28562897 28562897 28562897 CAGGGGTTCAAGACCAGCCTGGGCAACATGGCAAAACCCCATCTCTACAAAAAATAAAAAAAATT CAGGGGTTCAAGACCAGCCTGGGCAACATGGCGAAACCCCATCTCTACAAAAAATAAAAAAAATT T C AC005726.1,PIGS Ensembl:ENSG00000258472,Ensembl:ENSG00000087111 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs936341280 Functional Loss SNV dbSNP153 33..33 33 - - - 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 6661 RMVar_ID_6661 Human_SNP_ID_621171009 A-to-I Human chr17 - 28562897 28562897 28562897 CAGGGGTTCAAGACCAGCCTGGGCAACATGGCAAAACCCCATCTCTACAAAAAATAAAAAAAATT CAGGGGTTCAAGACCAGCCTGGGCAACATGGCCAAACCCCATCTCTACAAAAAATAAAAAAAATT T G AC005726.1,PIGS Ensembl:ENSG00000258472,Ensembl:ENSG00000087111 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs936341280 Functional Loss SNV dbSNP153 33..33 33 - - - 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 6662 RMVar_ID_6662 Human_SNP_ID_621171011 A-to-I Human chr17 - 28562902 28562902 28562902 GAACTCAGGGGTTCAAGACCAGCCTGGGCAACATGGCAAAACCCCATCTCTACAAAAAATAAAAA GAACTCAGGGGTTCAAGACCAGCCTGGGCAACGTGGCAAAACCCCATCTCTACAAAAAATAAAAA T C AC005726.1,PIGS Ensembl:ENSG00000258472,Ensembl:ENSG00000087111 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1480369642 Functional Loss SNV dbSNP153 33..33 33 - - - 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 6663 RMVar_ID_6663 Human_SNP_ID_621171014 A-to-I Human chr17 - 28562920 28562920 28562920 GAGGCGGGCAGTTTGCTTGAACTCAGGGGTTCAAGACCAGCCTGGGCAACATGGCAAAACCCCAT GAGGCGGGCAGTTTGCTTGAACTCAGGGGTTCGAGACCAGCCTGGGCAACATGGCAAAACCCCAT T C AC005726.1,PIGS Ensembl:ENSG00000258472,Ensembl:ENSG00000087111 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1261022786 Functional Loss SNV dbSNP153 33..33 33 - - - 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 6664 RMVar_ID_6664 Human_SNP_ID_621171647 A-to-I Human chr17 - 28565672 28565672 28565672 GTTCCCCGAGCTGGTCTCAAACTCCTAGGCTTAAGCAATCTTCCCACCTCGGACCCTAAAGTGCT GTTCCCCGAGCTGGTCTCAAACTCCTAGGCTTTAGCAATCTTCCCACCTCGGACCCTAAAGTGCT T A AC005726.1,PIGS Ensembl:ENSG00000258472,Ensembl:ENSG00000087111 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1216298824 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17566377 RMVar_hsa_circ_97593,RMVar_hsa_circ_88032,RMVar_hsa_circ_182849,RMVar_hsa_circ_182848 6665 RMVar_ID_6665 Human_SNP_ID_621171704 A-to-I Human chr17 - 28565864 28565864 28565864 CACCATGCCTGGCTAATTTTTGTAATTTTAGTAGAAACGGGGTTTCACCATGGTGGCCAGGCTGG CACCATGCCTGGCTAATTTTTGTAATTTTAGTGGAAACGGGGTTTCACCATGGTGGCCAGGCTGG T C AC005726.1,PIGS Ensembl:ENSG00000258472,Ensembl:ENSG00000087111 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1306533928 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97593,RMVar_hsa_circ_88032,RMVar_hsa_circ_182849,RMVar_hsa_circ_182848 6666 RMVar_ID_6666 Human_SNP_ID_621177491 A-to-I Human chr17 - 28588774 28588774 28588774 GGGTGGCTGAGGCATGAGAATTGCTTGAACCTAGGAGGTAGAGGTTGCAGTGAGCCGAGATCACC GGGTGGCTGAGGCATGAGAATTGCTTGAACCTGGGAGGTAGAGGTTGCAGTGAGCCGAGATCACC T C AC005726.1,SPAG5 Ensembl:ENSG00000258472,Ensembl:ENSG00000076382 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1207647253 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12939304 RMVar_hsa_circ_112923,RMVar_hsa_circ_182867,RMVar_hsa_circ_63792,RMVar_hsa_circ_182870,RMVar_hsa_circ_84737,RMVar_hsa_circ_118253,RMVar_hsa_circ_182871 6667 RMVar_ID_6667 Human_SNP_ID_621177503 A-to-I Human chr17 - 28588819 28588819 28588819 AAGTTAGCTGGGTATGGTAGTGCACTCCTGTAATCCCAGCTACTTGGGTGGCTGAGGCATGAGAA AAGTTAGCTGGGTATGGTAGTGCACTCCTGTAGTCCCAGCTACTTGGGTGGCTGAGGCATGAGAA T C AC005726.1,SPAG5 Ensembl:ENSG00000258472,Ensembl:ENSG00000076382 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1337730742 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112923,RMVar_hsa_circ_182867,RMVar_hsa_circ_63792,RMVar_hsa_circ_182870,RMVar_hsa_circ_84737,RMVar_hsa_circ_118253,RMVar_hsa_circ_182871 6668 RMVar_ID_6668 Human_SNP_ID_621177506 A-to-I Human chr17 - 28588833 28588833 28588833 TATTAAAAATACAAAAGTTAGCTGGGTATGGTAGTGCACTCCTGTAATCCCAGCTACTTGGGTGG TATTAAAAATACAAAAGTTAGCTGGGTATGGTCGTGCACTCCTGTAATCCCAGCTACTTGGGTGG T G AC005726.1,SPAG5 Ensembl:ENSG00000258472,Ensembl:ENSG00000076382 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1170409078 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112923,RMVar_hsa_circ_182867,RMVar_hsa_circ_63792,RMVar_hsa_circ_182870,RMVar_hsa_circ_84737,RMVar_hsa_circ_118253,RMVar_hsa_circ_182871 6669 RMVar_ID_6669 Human_SNP_ID_621178439 A-to-I Human chr17 - 28592667 28592667 28592667 TTTCAGAAGTTGCTGCTGTATCTGAGAAACCTATCTTTCAGGAATCTCCGTCCCATCTCTTAGAG TTTCAGAAGTTGCTGCTGTATCTGAGAAACCTGTCTTTCAGGAATCTCCGTCCCATCTCTTAGAG T C AC005726.1,SPAG5 Ensembl:ENSG00000258472,Ensembl:ENSG00000076382 Protein coding,Protein coding intron,CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1230843129 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1285202,Human_RBP_ID_3951982,Human_RBP_ID_12939373,Human_RBP_ID_22061146 Human_miRNA_ID_2135153,Human_miRNA_ID_2701600 RMVar_hsa_circ_112923,RMVar_hsa_circ_182867,RMVar_hsa_circ_182870,RMVar_hsa_circ_84737,RMVar_hsa_circ_118253,RMVar_hsa_circ_182871,RMVar_hsa_circ_306509,RMVar_hsa_circ_182874,RMVar_hsa_circ_182875,RMVar_hsa_circ_123990,RMVar_hsa_circ_182876 6670 RMVar_ID_6670 Human_SNP_ID_621182574 A-to-I Human chr17 - 28606842 28606842 28606842 CCTCAGGTAATTCACTCGTCTTGGCCTTCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCTCC CCTCAGGTAATTCACTCGTCTTGGCCTTCCAAGGTGCTGGGATTACAGGCGTGAGCCACTGCTCC T C AC005726.1,RSKR Ensembl:ENSG00000258472,Ensembl:ENSG00000167524 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1050684315 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23167694 6671 RMVar_ID_6671 Human_SNP_ID_621182640 A-to-I Human chr17 - 28607110 28607106 28607111 CTGTGATGCTTTTTCTTTCTTTTTTTTTTTTGAGACTGAGTTTTGCTCTTGTCACCCAGACTGGA CTGTGATGCTTTTTCTTTCTTTTTTTTTTTT_____TGAGTTTTGCTCTTGTCACCCAGACTGGA AGTCTC A AC005726.1,RSKR Ensembl:ENSG00000258472,Ensembl:ENSG00000167524 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1176301666 Functional Loss DEL dbSNP153 32..36 33 - - - Human_RBP_ID_6573153,Human_RBP_ID_17565533 6672 RMVar_ID_6672 Human_SNP_ID_621182772 A-to-I Human chr17 - 28607658 28607658 28607658 TCACTGTAGCCTCTGCCTCCCAGGTTCTAGCAATTCTCCTGCCTCAGCCTCGTGGGTAGCTGGGA TCACTGTAGCCTCTGCCTCCCAGGTTCTAGCAGTTCTCCTGCCTCAGCCTCGTGGGTAGCTGGGA T C AC005726.1,RSKR Ensembl:ENSG00000258472,Ensembl:ENSG00000167524 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs995405803 Functional Loss SNV dbSNP153 33..33 33 - - - 6673 RMVar_ID_6673 Human_SNP_ID_621182941 A-to-I Human chr17 - 28608412 28608412 28608412 AGATGGAGGTTGCAATGAGTGAAGATCGTGCCACTGCATCCAGCCTGAGCAACAGAGTGAGATCT AGATGGAGGTTGCAATGAGTGAAGATCGTGCCGCTGCATCCAGCCTGAGCAACAGAGTGAGATCT T C AC005726.1,RSKR Ensembl:ENSG00000258472,Ensembl:ENSG00000167524 Protein coding,Protein coding intron,intron GSE47997;GSE100210;GSE107867;GSE107867 K562 cells&HepG2 cells;HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank;ASD brains,temporal_cortex - 23474544,29129909,30559470,30559470 RNA-Seq:(High) rs1386384955 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6573174,Human_RBP_ID_12939550 6674 RMVar_ID_6674 Human_SNP_ID_621182944 A-to-I Human chr17 - 28608423 28608423 28608423 TTGAACCCAGGAGATGGAGGTTGCAATGAGTGAAGATCGTGCCACTGCATCCAGCCTGAGCAACA TTGAACCCAGGAGATGGAGGTTGCAATGAGTGGAGATCGTGCCACTGCATCCAGCCTGAGCAACA T C AC005726.1,RSKR Ensembl:ENSG00000258472,Ensembl:ENSG00000167524 Protein coding,Protein coding intron,intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1008124247 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12939550 6675 RMVar_ID_6675 Human_SNP_ID_621182945 A-to-I Human chr17 - 28608423 28608423 28608423 TTGAACCCAGGAGATGGAGGTTGCAATGAGTGAAGATCGTGCCACTGCATCCAGCCTGAGCAACA TTGAACCCAGGAGATGGAGGTTGCAATGAGTGCAGATCGTGCCACTGCATCCAGCCTGAGCAACA T G AC005726.1,RSKR Ensembl:ENSG00000258472,Ensembl:ENSG00000167524 Protein coding,Protein coding intron,intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1008124247 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12939550 6676 RMVar_ID_6676 Human_SNP_ID_621182948 A-to-I Human chr17 - 28608430 28608430 28608430 GAATTGCTTGAACCCAGGAGATGGAGGTTGCAATGAGTGAAGATCGTGCCACTGCATCCAGCCTG GAATTGCTTGAACCCAGGAGATGGAGGTTGCAGTGAGTGAAGATCGTGCCACTGCATCCAGCCTG T C AC005726.1,RSKR Ensembl:ENSG00000258472,Ensembl:ENSG00000167524 Protein coding,Protein coding intron,intron GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs569659960 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12939551,Human_RBP_ID_25260270 6677 RMVar_ID_6677 Human_SNP_ID_621182955 A-to-I Human chr17 - 28608479 28608479 28608479 CATGAGGGCACACACTGTAGTCCCAGCTACTCAGGAGGCTGAGGGGGAAGAATTGCTTGAACCCA CATGAGGGCACACACTGTAGTCCCAGCTACTCCGGAGGCTGAGGGGGAAGAATTGCTTGAACCCA T G AC005726.1,RSKR Ensembl:ENSG00000258472,Ensembl:ENSG00000167524 Protein coding,Protein coding intron,intron GSE47997;GSE38233;GSE100210;GSE107867 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;ASD brains,temporal_cortex - 23474544,24183664,29129909,30559470 RNA-Seq:(High) rs1359551538 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12939553 6678 RMVar_ID_6678 Human_SNP_ID_621182958 A-to-I Human chr17 - 28608493 28608493 28608493 AAAAATTAGCTGGTCATGAGGGCACACACTGTAGTCCCAGCTACTCAGGAGGCTGAGGGGGAAGA AAAAATTAGCTGGTCATGAGGGCACACACTGTGGTCCCAGCTACTCAGGAGGCTGAGGGGGAAGA T C AC005726.1,RSKR Ensembl:ENSG00000258472,Ensembl:ENSG00000167524 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs879318545 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12939553 6679 RMVar_ID_6679 Human_SNP_ID_621182962 A-to-I Human chr17 - 28608518 28608518 28608518 AACCCCGTTTCTCCCCAAAAAATACAAAAATTAGCTGGTCATGAGGGCACACACTGTAGTCCCAG AACCCCGTTTCTCCCCAAAAAATACAAAAATTTGCTGGTCATGAGGGCACACACTGTAGTCCCAG T A AC005726.1,RSKR Ensembl:ENSG00000258472,Ensembl:ENSG00000167524 Protein coding,Protein coding intron,intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs903500961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12939553 6680 RMVar_ID_6680 Human_SNP_ID_621182964 A-to-I Human chr17 - 28608533 28608533 28608533 TGGCCAACATGGTGAAACCCCGTTTCTCCCCAAAAAATACAAAAATTAGCTGGTCATGAGGGCAC TGGCCAACATGGTGAAACCCCGTTTCTCCCCAGAAAATACAAAAATTAGCTGGTCATGAGGGCAC T C AC005726.1,RSKR Ensembl:ENSG00000258472,Ensembl:ENSG00000167524 Protein coding,Protein coding intron,intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1425155764 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25260273 6681 RMVar_ID_6681 Human_SNP_ID_621182965 A-to-I Human chr17 - 28608534 28608534 28608534 CTGGCCAACATGGTGAAACCCCGTTTCTCCCCAAAAAATACAAAAATTAGCTGGTCATGAGGGCA CTGGCCAACATGGTGAAACCCCGTTTCTCCCCCAAAAATACAAAAATTAGCTGGTCATGAGGGCA T G AC005726.1,RSKR Ensembl:ENSG00000258472,Ensembl:ENSG00000167524 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs997077384 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25260273 6682 RMVar_ID_6682 Human_SNP_ID_621183119 A-to-I Human chr17 - 28609115 28609115 28609115 AGAACTGCTTGAACCCTGGAGGCCAAGGTTGCAGTGAGCCAAGATTGTGCCATTGAACTCCTGGG AGAACTGCTTGAACCCTGGAGGCCAAGGTTGCGGTGAGCCAAGATTGTGCCATTGAACTCCTGGG T C AC005726.1,RSKR Ensembl:ENSG00000258472,Ensembl:ENSG00000167524 Protein coding,Protein coding intron,intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs543307824 Functional Loss SNV dbSNP153 33..33 33 - - - 6683 RMVar_ID_6683 Human_SNP_ID_621183127 A-to-I Human chr17 - 28609153 28609153 28609153 ACACCTGTAGTCCCAGCTACTCAGAAGGCTGAAGCAGGAGAACTGCTTGAACCCTGGAGGCCAAG ACACCTGTAGTCCCAGCTACTCAGAAGGCTGAGGCAGGAGAACTGCTTGAACCCTGGAGGCCAAG T C AC005726.1,RSKR Ensembl:ENSG00000258472,Ensembl:ENSG00000167524 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs950869893 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12939571,Human_RBP_ID_25260281 6684 RMVar_ID_6684 Human_SNP_ID_621183279 A-to-I Human chr17 - 28609809 28609809 28609809 ACCTCAAGTGATCGGCCTGCCTTGGCCTCCCAAAGTGCTGGAATTACAGGTAGGTGTGAGCCACT ACCTCAAGTGATCGGCCTGCCTTGGCCTCCCAGAGTGCTGGAATTACAGGTAGGTGTGAGCCACT T C AC005726.1,RSKR Ensembl:ENSG00000258472,Ensembl:ENSG00000167524 Protein coding,Protein coding intron,intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs994456378 Functional Loss SNV dbSNP153 33..33 33 - - - 6685 RMVar_ID_6685 Human_SNP_ID_621188478 A-to-I Human chr17 - 28628334 28628334 28628334 CAGCCAAAAAGCCAAAGCGGGGTGTCCCAACTAGTGCCTCAGCCCCACCTCGTGTTAACACTCCC CAGCCAAAAAGCCAAAGCGGGGTGTCCCAACTGGTGCCTCAGCCCCACCTCGTGTTAACACTCCC T C KIAA0100 Ensembl:ENSG00000007202 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1190032738 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_485866,Human_RBP_ID_5114587,Human_RBP_ID_26812043 Human_Splice_Rec_1796133,Human_Splice_Rec_1796207,Human_Splice_Rec_1796281 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_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_309752,RMVar_hsa_circ_278938,RMVar_hsa_circ_90520,RMVar_hsa_circ_96387,RMVar_hsa_circ_4594,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_182916,RMVar_hsa_circ_182918,RMVar_hsa_circ_83485,RMVar_hsa_circ_182917,RMVar_hsa_circ_292052 6686 RMVar_ID_6686 Human_SNP_ID_621188585 A-to-I Human chr17 - 28628785 28628785 28628785 GGATTACCAGTGCCAGCCACCATGCCCAGCTAATTTTTTGTATTTTTAGTAGAGATGGGGTTTCA GGATTACCAGTGCCAGCCACCATGCCCAGCTACTTTTTTGTATTTTTAGTAGAGATGGGGTTTCA T G KIAA0100 Ensembl:ENSG00000007202 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1396860190 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25260479 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_182916,RMVar_hsa_circ_182918,RMVar_hsa_circ_83485,RMVar_hsa_circ_182917 6687 RMVar_ID_6687 Human_SNP_ID_621188615 A-to-I Human chr17 - 28628903 28628903 28628903 TTGAGACTGCGTCTCTCTCTGTCGCCTGGGCTAGAGTGCAGTGGTGTGATCTCGGCTCACTGCAA TTGAGACTGCGTCTCTCTCTGTCGCCTGGGCTGGAGTGCAGTGGTGTGATCTCGGCTCACTGCAA T C KIAA0100 Ensembl:ENSG00000007202 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs974662558 Functional Loss SNV dbSNP153 33..33 33 - - - 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_182916,RMVar_hsa_circ_182918,RMVar_hsa_circ_83485,RMVar_hsa_circ_182917 6688 RMVar_ID_6688 Human_SNP_ID_621188753 A-to-I Human chr17 - 28629405 28629405 28629405 ATACCTGTAATCCCCAGGTACTTGGAGACTGAAGCATGAGAATCGCTTGAACCTGGGAGGCAGAG ATACCTGTAATCCCCAGGTACTTGGAGACTGAGGCATGAGAATCGCTTGAACCTGGGAGGCAGAG T C KIAA0100 Ensembl:ENSG00000007202 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs543710083 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6573257,Human_RBP_ID_12939961 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_182916,RMVar_hsa_circ_182918,RMVar_hsa_circ_83485,RMVar_hsa_circ_182917 6689 RMVar_ID_6689 Human_SNP_ID_621190486 A-to-I Human chr17 - 28635071 28635071 28635071 TCCTTATCAGTATGACTTTTCTCGAACTCTAGATGAGGCTGTGGGAGTTCAGAAGTGGCTGAAGG TCCTTATCAGTATGACTTTTCTCGAACTCTAGTTGAGGCTGTGGGAGTTCAGAAGTGGCTGAAGG T A KIAA0100 Ensembl:ENSG00000007202 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs752231198 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1530159,Human_RBP_ID_1852123,Human_RBP_ID_3516374,Human_RBP_ID_5525451,Human_RBP_ID_8814937,Human_RBP_ID_9258200,Human_RBP_ID_9288855,Human_RBP_ID_12940015,Human_RBP_ID_22061161,Human_RBP_ID_26957642 Human_miRNA_ID_2797952,Human_miRNA_ID_2798918,Human_miRNA_ID_2800299,Human_miRNA_ID_2807614,Human_miRNA_ID_2810758,Human_miRNA_ID_2813900,Human_miRNA_ID_2833490,Human_miRNA_ID_2853013,Human_miRNA_ID_2854075,Human_miRNA_ID_2861157,Human_miRNA_ID_2868595 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 6690 RMVar_ID_6690 Human_SNP_ID_621190487 A-to-I Human chr17 - 28635071 28635071 28635071 TCCTTATCAGTATGACTTTTCTCGAACTCTAGATGAGGCTGTGGGAGTTCAGAAGTGGCTGAAGG TCCTTATCAGTATGACTTTTCTCGAACTCTAGGTGAGGCTGTGGGAGTTCAGAAGTGGCTGAAGG T C KIAA0100 Ensembl:ENSG00000007202 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs752231198 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1530159,Human_RBP_ID_1852123,Human_RBP_ID_3516374,Human_RBP_ID_5525451,Human_RBP_ID_8814937,Human_RBP_ID_9258200,Human_RBP_ID_9288855,Human_RBP_ID_12940015,Human_RBP_ID_22061161,Human_RBP_ID_26957642 Human_miRNA_ID_2797952,Human_miRNA_ID_2798918,Human_miRNA_ID_2800299,Human_miRNA_ID_2807614,Human_miRNA_ID_2810758,Human_miRNA_ID_2813900,Human_miRNA_ID_2833490,Human_miRNA_ID_2853013,Human_miRNA_ID_2854075,Human_miRNA_ID_2861157,Human_miRNA_ID_2868595 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 6691 RMVar_ID_6691 Human_SNP_ID_621195789 A-to-I Human chr17 - 28652181 28652181 28652181 ATGAGCTTTCTTTTTCTTTTTCTTTTTTTTTTAAGATGGGTTCTTGCTGTGTTATTCAGGCTGGA ATGAGCTTTCTTTTTCTTTTTCTTTTTTTTTTTAGATGGGTTCTTGCTGTGTTATTCAGGCTGGA T A SDF2 Ensembl:ENSG00000132581 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1209108725 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6661220 RMVar_hsa_circ_182959,RMVar_hsa_circ_291816 6692 RMVar_ID_6692 Human_SNP_ID_621195790 A-to-I Human chr17 - 28652181 28652181 28652181 ATGAGCTTTCTTTTTCTTTTTCTTTTTTTTTTAAGATGGGTTCTTGCTGTGTTATTCAGGCTGGA ATGAGCTTTCTTTTTCTTTTTCTTTTTTTTTTGAGATGGGTTCTTGCTGTGTTATTCAGGCTGGA T C SDF2 Ensembl:ENSG00000132581 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1209108725 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6661220 RMVar_hsa_circ_182959,RMVar_hsa_circ_291816 6693 RMVar_ID_6693 Human_SNP_ID_621195862 A-to-I Human chr17 - 28652475 28652475 28652475 TGAAACCCCGTATCTACTAAAGTACAAAAATTAGCTGGGCATGGTGGCGGGAGCCTGTGATCCCA TGAAACCCCGTATCTACTAAAGTACAAAAATTCGCTGGGCATGGTGGCGGGAGCCTGTGATCCCA T G SDF2 Ensembl:ENSG00000132581 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042333046 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_182959,RMVar_hsa_circ_291816 6694 RMVar_ID_6694 Human_SNP_ID_621197280 A-to-I Human chr17 - 28657915 28657915 28657915 GACCTCCTGGGCTCAAGCAATCCTCACATCTCAGCGTCCTGAGTAGCTGGGACTACAAGTGCACC GACCTCCTGGGCTCAAGCAATCCTCACATCTCGGCGTCCTGAGTAGCTGGGACTACAAGTGCACC T C SDF2 Ensembl:ENSG00000132581 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs891303542 Functional Loss SNV dbSNP153 33..33 33 - - - 6695 RMVar_ID_6695 Human_SNP_ID_621197294 A-to-I Human chr17 - 28657968 28657968 28657968 CTACATTTACCCGTGTAACTGGCAGTGACACAATTACGACTCATTGCAGCCTTGACCTCCTGGGC CTACATTTACCCGTGTAACTGGCAGTGACACAGTTACGACTCATTGCAGCCTTGACCTCCTGGGC T C SDF2 Ensembl:ENSG00000132581 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs981007891 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12940390 6696 RMVar_ID_6696 Human_SNP_ID_621200003 A-to-I Human chr17 + 28666607 28666607 28666607 GGAGTCTCGCTCTGTCACCTTGGCTGGAGTGCAATGGCATGATCTCGACTCACTGCAAGCTCTGA GGAGTCTCGCTCTGTCACCTTGGCTGGAGTGCGATGGCATGATCTCGACTCACTGCAAGCTCTGA A G SUPT6H Ensembl:ENSG00000109111 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs990714916 Functional Loss SNV dbSNP153 33..33 33 - - - 6697 RMVar_ID_6697 Human_SNP_ID_621200005 A-to-I Human chr17 + 28666613 28666613 28666613 TCGCTCTGTCACCTTGGCTGGAGTGCAATGGCATGATCTCGACTCACTGCAAGCTCTGACTCCCA TCGCTCTGTCACCTTGGCTGGAGTGCAATGGCCTGATCTCGACTCACTGCAAGCTCTGACTCCCA A C SUPT6H Ensembl:ENSG00000109111 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs940728995 Functional Loss SNV dbSNP153 33..33 33 - - - 6698 RMVar_ID_6698 Human_SNP_ID_621200018 A-to-I Human chr17 + 28666669 28666669 28666669 TGACTCCCACGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCGTGCA TGACTCCCACGTTCAAGCGATTCTCCTGCCTCGGCCTCCTGAGTAGCTGGGATTACAGGCGTGCA A G SUPT6H Ensembl:ENSG00000109111 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs550316422 Functional Loss SNV dbSNP153 33..33 33 - - - 6699 RMVar_ID_6699 Human_SNP_ID_621200029 A-to-I Human chr17 + 28666717 28666717 28666717 GGGATTACAGGCGTGCACCACCACACCCGGCTAATTTTTGTATTTTTAGTGGAGACAGGGTTTCA GGGATTACAGGCGTGCACCACCACACCCGGCTGATTTTTGTATTTTTAGTGGAGACAGGGTTTCA A G SUPT6H Ensembl:ENSG00000109111 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1038610204 Functional Loss SNV dbSNP153 33..33 33 - - - 6700 RMVar_ID_6700 Human_SNP_ID_621200031 A-to-I Human chr17 + 28666732 28666732 28666732 CACCACCACACCCGGCTAATTTTTGTATTTTTAGTGGAGACAGGGTTTCATCATGCTGGCCAGGC CACCACCACACCCGGCTAATTTTTGTATTTTTGGTGGAGACAGGGTTTCATCATGCTGGCCAGGC A G SUPT6H Ensembl:ENSG00000109111 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1009901879 Functional Loss SNV dbSNP153 33..33 33 - - - 6701 RMVar_ID_6701 Human_SNP_ID_621200034 A-to-I Human chr17 + 28666741 28666741 28666741 ACCCGGCTAATTTTTGTATTTTTAGTGGAGACAGGGTTTCATCATGCTGGCCAGGCTGGTCTCGA ACCCGGCTAATTTTTGTATTTTTAGTGGAGACTGGGTTTCATCATGCTGGCCAGGCTGGTCTCGA A T SUPT6H Ensembl:ENSG00000109111 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1209582666 Functional Loss SNV dbSNP153 33..33 33 - - - 6702 RMVar_ID_6702 Human_SNP_ID_621201056 A-to-I Human chr17 + 28669923 28669923 28669923 GTGCCATTGCACTTCATCCTGGGTGAGAGAGTAAGACTCTGTCTCAAAATAAGTAAATTAAGTAA GTGCCATTGCACTTCATCCTGGGTGAGAGAGTGAGACTCTGTCTCAAAATAAGTAAATTAAGTAA A G SUPT6H Ensembl:ENSG00000109111 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1031121284 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6573427 6703 RMVar_ID_6703 Human_SNP_ID_621201650 A-to-I Human chr17 + 28672500 28672500 28672500 CAGTGGTGCAATCTCAGCTCACTGCAACCTCCACCTCCCGGGGTCAAACCATTCTCCTGCCTAAG CAGTGGTGCAATCTCAGCTCACTGCAACCTCCGCCTCCCGGGGTCAAACCATTCTCCTGCCTAAG A G SUPT6H Ensembl:ENSG00000109111 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459918517 Functional Loss SNV dbSNP153 33..33 33 - - - 6704 RMVar_ID_6704 Human_SNP_ID_621201711 A-to-I Human chr17 + 28672744 28672744 28672744 CCTAATGGCTTTTTTTTTTAAGACAGAGTCTCACTCTCTCGCCAGGCTGGAATGCAGTGGCGCAA CCTAATGGCTTTTTTTTTTAAGACAGAGTCTCTCTCTCTCGCCAGGCTGGAATGCAGTGGCGCAA A T SUPT6H Ensembl:ENSG00000109111 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1158047616 Functional Loss SNV dbSNP153 33..33 33 - - - 6705 RMVar_ID_6705 Human_SNP_ID_621201731 A-to-I Human chr17 + 28672802 28672802 28672802 GGCGCAATCTGCAACCTCCACCTTCCGGATTCAAGAGATTCTCCTGCCTCAGCCTCCTGAGTAGC GGCGCAATCTGCAACCTCCACCTTCCGGATTCCAGAGATTCTCCTGCCTCAGCCTCCTGAGTAGC A C SUPT6H Ensembl:ENSG00000109111 Protein coding 5'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs182501709 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12940711,Human_RBP_ID_25260804 Human_Splice_Rec_1796456,Human_Splice_Rec_1796457 Human_miRNA_ID_2233366 RMVar_hsa_circ_124875,RMVar_hsa_circ_182961 6706 RMVar_ID_6706 Human_SNP_ID_621212006 A-to-I Human chr17 - 28709794 28709794 28709794 AGGGATTTCACCATGTTGACCATGCTGGTCTCAAACTCCGGACCTCAAGTGATCCGCCCACCTCG AGGGATTTCACCATGTTGACCATGCTGGTCTCGAACTCCGGACCTCAAGTGATCCGCCCACCTCG T C PROCA1 Ensembl:ENSG00000167525 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1051163272 Functional Loss SNV dbSNP153 33..33 33 - - - 6707 RMVar_ID_6707 Human_SNP_ID_621212007 A-to-I Human chr17 - 28709794 28709794 28709794 AGGGATTTCACCATGTTGACCATGCTGGTCTCAAACTCCGGACCTCAAGTGATCCGCCCACCTCG AGGGATTTCACCATGTTGACCATGCTGGTCTCCAACTCCGGACCTCAAGTGATCCGCCCACCTCG T G PROCA1 Ensembl:ENSG00000167525 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1051163272 Functional Loss SNV dbSNP153 33..33 33 - - - 6708 RMVar_ID_6708 Human_SNP_ID_621212014 A-to-I Human chr17 - 28709814 28709814 28709814 TTTTGGATTTTTATTAGAGAAGGGATTTCACCATGTTGACCATGCTGGTCTCAAACTCCGGACCT TTTTGGATTTTTATTAGAGAAGGGATTTCACCTTGTTGACCATGCTGGTCTCAAACTCCGGACCT T A PROCA1 Ensembl:ENSG00000167525 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1235573920 Functional Loss SNV dbSNP153 33..33 33 - - - 6709 RMVar_ID_6709 Human_SNP_ID_621212015 A-to-I Human chr17 - 28709814 28709814 28709814 TTTTGGATTTTTATTAGAGAAGGGATTTCACCATGTTGACCATGCTGGTCTCAAACTCCGGACCT TTTTGGATTTTTATTAGAGAAGGGATTTCACCGTGTTGACCATGCTGGTCTCAAACTCCGGACCT T C PROCA1 Ensembl:ENSG00000167525 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1235573920 Functional Loss SNV dbSNP153 33..33 33 - - - 6710 RMVar_ID_6710 Human_SNP_ID_621212172 A-to-I Human chr17 - 28710421 28710421 28710421 CTCACTGCAAACTCCACCTCCCGGGTTCAAACAATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGG CTCACTGCAAACTCCACCTCCCGGGTTCAAACGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGG T C PROCA1 Ensembl:ENSG00000167525 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs949417905 Functional Loss SNV dbSNP153 33..33 33 - - - 6711 RMVar_ID_6711 Human_SNP_ID_621212180 A-to-I Human chr17 - 28710450 28710450 28710450 CAGGCTGGAGTGCAGTGGCGCAATATCGGCTCACTGCAAACTCCACCTCCCGGGTTCAAACAATT CAGGCTGGAGTGCAGTGGCGCAATATCGGCTCGCTGCAAACTCCACCTCCCGGGTTCAAACAATT T C PROCA1 Ensembl:ENSG00000167525 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1002440814 Functional Loss SNV dbSNP153 33..33 33 - - - 6712 RMVar_ID_6712 Human_SNP_ID_621216130 A-to-I Human chr17 + 28722308 28722308 28722308 TGGCCCGATTCTCCTGCCTCAGCCTCTTGAGTAGCTCGGACTACAGGCGTGCACCACCATGACCA TGGCCCGATTCTCCTGCCTCAGCCTCTTGAGTGGCTCGGACTACAGGCGTGCACCACCATGACCA A G RPL23A Ensembl:ENSG00000198242 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1032363853 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75810,RMVar_hsa_circ_81228,RMVar_hsa_circ_183005,RMVar_hsa_circ_124131,RMVar_hsa_circ_183007,RMVar_hsa_circ_92588,RMVar_hsa_circ_183009,RMVar_hsa_circ_183010 6713 RMVar_ID_6713 Human_SNP_ID_621216134 A-to-I Human chr17 + 28722320 28722320 28722320 CCTGCCTCAGCCTCTTGAGTAGCTCGGACTACAGGCGTGCACCACCATGACCAGCTAATTTTTGT CCTGCCTCAGCCTCTTGAGTAGCTCGGACTACGGGCGTGCACCACCATGACCAGCTAATTTTTGT A G RPL23A Ensembl:ENSG00000198242 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1009508259 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75810,RMVar_hsa_circ_81228,RMVar_hsa_circ_183005,RMVar_hsa_circ_124131,RMVar_hsa_circ_183007,RMVar_hsa_circ_92588,RMVar_hsa_circ_183009,RMVar_hsa_circ_183010 6714 RMVar_ID_6714 Human_SNP_ID_621216142 A-to-I Human chr17 + 28722359 28722359 28722359 CACCACCATGACCAGCTAATTTTTGTATTTTTAGTTGAGAGGGAGTTTCACCATGTTGGCCAGGA CACCACCATGACCAGCTAATTTTTGTATTTTTGGTTGAGAGGGAGTTTCACCATGTTGGCCAGGA A G RPL23A Ensembl:ENSG00000198242 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1056506385 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12940939 RMVar_hsa_circ_75810,RMVar_hsa_circ_81228,RMVar_hsa_circ_183005,RMVar_hsa_circ_124131,RMVar_hsa_circ_183007,RMVar_hsa_circ_92588,RMVar_hsa_circ_183009,RMVar_hsa_circ_183010 6715 RMVar_ID_6715 Human_SNP_ID_621216148 A-to-I Human chr17 + 28722379 28722370 28722380 TTTTGTATTTTTAGTTGAGAGGGAGTTTCACCATGTTGGCCAGGATGGTCACGATCTCTTGACCT TTTTGTATTTTTAGTTGAGAGGGA__________GTTGGCCAGGATGGTCACGATCTCTTGACCT AGTTTCACCAT A RPL23A Ensembl:ENSG00000198242 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1331280895 Functional Loss DEL dbSNP153 25..34 33 - - - Human_RBP_ID_12940940,Human_RBP_ID_25260962 RMVar_hsa_circ_75810,RMVar_hsa_circ_81228,RMVar_hsa_circ_183005,RMVar_hsa_circ_124131,RMVar_hsa_circ_183007,RMVar_hsa_circ_92588,RMVar_hsa_circ_183009,RMVar_hsa_circ_183010 6716 RMVar_ID_6716 Human_SNP_ID_621216151 A-to-I Human chr17 + 28722376 28722376 28722376 AATTTTTGTATTTTTAGTTGAGAGGGAGTTTCACCATGTTGGCCAGGATGGTCACGATCTCTTGA AATTTTTGTATTTTTAGTTGAGAGGGAGTTTCGCCATGTTGGCCAGGATGGTCACGATCTCTTGA A G RPL23A Ensembl:ENSG00000198242 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1387255993 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12940940 RMVar_hsa_circ_75810,RMVar_hsa_circ_81228,RMVar_hsa_circ_183005,RMVar_hsa_circ_124131,RMVar_hsa_circ_183007,RMVar_hsa_circ_92588,RMVar_hsa_circ_183009,RMVar_hsa_circ_183010 6717 RMVar_ID_6717 Human_SNP_ID_621216152 A-to-I Human chr17 + 28722379 28722379 28722379 TTTTGTATTTTTAGTTGAGAGGGAGTTTCACCATGTTGGCCAGGATGGTCACGATCTCTTGACCT TTTTGTATTTTTAGTTGAGAGGGAGTTTCACCTTGTTGGCCAGGATGGTCACGATCTCTTGACCT A T RPL23A Ensembl:ENSG00000198242 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs562504887 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12940940,Human_RBP_ID_25260962 RMVar_hsa_circ_75810,RMVar_hsa_circ_81228,RMVar_hsa_circ_183005,RMVar_hsa_circ_124131,RMVar_hsa_circ_183007,RMVar_hsa_circ_92588,RMVar_hsa_circ_183009,RMVar_hsa_circ_183010 6718 RMVar_ID_6718 Human_SNP_ID_621216153 A-to-I Human chr17 + 28722388 28722388 28722388 TTTAGTTGAGAGGGAGTTTCACCATGTTGGCCAGGATGGTCACGATCTCTTGACCTCGTGATCAG TTTAGTTGAGAGGGAGTTTCACCATGTTGGCCTGGATGGTCACGATCTCTTGACCTCGTGATCAG A T RPL23A Ensembl:ENSG00000198242 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1321192171 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75810,RMVar_hsa_circ_81228,RMVar_hsa_circ_183005,RMVar_hsa_circ_124131,RMVar_hsa_circ_183007,RMVar_hsa_circ_92588,RMVar_hsa_circ_183009,RMVar_hsa_circ_183010 6719 RMVar_ID_6719 Human_SNP_ID_621216166 A-to-I Human chr17 + 28722437 28722436 28722437 TTGACCTCGTGATCAGCCTGCCTCAGCCTCCCAAAGTGCTGGGAATACAGCCATGAGCCAGCACA TTGACCTCGTGATCAGCCTGCCTCAGCCTCCC_AAGTGCTGGGAATACAGCCATGAGCCAGCACA CA C RPL23A Ensembl:ENSG00000198242 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1261690876 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_75810,RMVar_hsa_circ_81228,RMVar_hsa_circ_183005,RMVar_hsa_circ_124131,RMVar_hsa_circ_183007,RMVar_hsa_circ_92588,RMVar_hsa_circ_183009,RMVar_hsa_circ_183010 6720 RMVar_ID_6720 Human_SNP_ID_621231491 A-to-I Human chr17 - 28771629 28771629 28771629 TTTCCCGGGCTGGTGTGCAGTGGCAAAATCTCAGCTCACGACAACCTCTGCCTCCCAGGTTCAAG TTTCCCGGGCTGGTGTGCAGTGGCAAAATCTCGGCTCACGACAACCTCTGCCTCCCAGGTTCAAG T C FAM222B Ensembl:ENSG00000173065 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs902267733 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_285541 6721 RMVar_ID_6721 Human_SNP_ID_621239074 A-to-I Human chr17 - 28799903 28799903 28799903 GTTTTCTTATTGTTTAAAGAGCCTTTCTTGCCAGGTGTGGTGACTCACACCTATAATCCTAGAAC GTTTTCTTATTGTTTAAAGAGCCTTTCTTGCCTGGTGTGGTGACTCACACCTATAATCCTAGAAC T A FAM222B Ensembl:ENSG00000173065 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1028265993 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17566800 6722 RMVar_ID_6722 Human_SNP_ID_621239807 A-to-I Human chr17 - 28802387 28802387 28802387 CACTTTAAAGCTGGGGGTTTCTGGCTGGGCGCAGTGGCTCATGTCTATAATCCCAGCACTTTGGG CACTTTAAAGCTGGGGGTTTCTGGCTGGGCGCGGTGGCTCATGTCTATAATCCCAGCACTTTGGG T C FAM222B Ensembl:ENSG00000173065 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs966176304 Functional Loss SNV dbSNP153 33..33 33 - - - 6723 RMVar_ID_6723 Human_SNP_ID_621242000 A-to-I Human chr17 - 28811357 28811357 28811357 CGGCTCACTGCAACCTCTGCCTCCAGGGTTCAAGCGATTCCCCTGTCTTAGCCTCCTGAGTAGCT CGGCTCACTGCAACCTCTGCCTCCAGGGTTCAGGCGATTCCCCTGTCTTAGCCTCCTGAGTAGCT T C FAM222B Ensembl:ENSG00000173065 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1414066218 Functional Loss SNV dbSNP153 33..33 33 - - - 6724 RMVar_ID_6724 Human_SNP_ID_621242800 A-to-I Human chr17 - 28813700 28813700 28813700 CTACTAAAAAATACAAAAAAAAAAAAAAAATTAGCTGGGCGTGATGGCGGCCACCTGTAGTCCCA CTACTAAAAAATACAAAAAAAAAAAAAAAATTGGCTGGGCGTGATGGCGGCCACCTGTAGTCCCA T C FAM222B Ensembl:ENSG00000173065 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1442336939 Functional Loss SNV dbSNP153 33..33 33 - - - 6725 RMVar_ID_6725 Human_SNP_ID_621242927 A-to-I Human chr17 - 28814096 28814096 28814096 TGCTCACTGTACTCTGCCAAGTAGCTGGGACTACCGTGCGAGTTACCACGCCTAGCTACCTCTAA TGCTCACTGTACTCTGCCAAGTAGCTGGGACTGCCGTGCGAGTTACCACGCCTAGCTACCTCTAA T C FAM222B Ensembl:ENSG00000173065 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs550027479 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_767403 6726 RMVar_ID_6726 Human_SNP_ID_621244892 A-to-I Human chr17 - 28821919 28821919 28821919 GCTCTGTCGCCCAGGCTGGAGTGCAATGGTGCAATCTCGGCTCACTGCAACCTCTGCCCAGCCCC GCTCTGTCGCCCAGGCTGGAGTGCAATGGTGCGATCTCGGCTCACTGCAACCTCTGCCCAGCCCC T C FAM222B Ensembl:ENSG00000173065 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935732136 Functional Loss SNV dbSNP153 33..33 33 - - - 6727 RMVar_ID_6727 Human_SNP_ID_621245810 A-to-I Human chr17 - 28825037 28825037 28825037 ATTGTAGTGCGGGCACAGTGGTTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGCGG ATTGTAGTGCGGGCACAGTGGTTCACGCCTGTGATCCCAGCACTTTGGGAGGCCAAGGCGGGCGG T C FAM222B Ensembl:ENSG00000173065 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1372468553 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17565812 6728 RMVar_ID_6728 Human_SNP_ID_621245881 A-to-I Human chr17 - 28825341 28825341 28825341 TAACCTCCACCACCGGGCTAAGGGATCCTCCCACCCCAGCCTCTCAAGTAGCTGGGACCATAGGT TAACCTCCACCACCGGGCTAAGGGATCCTCCCCCCCCAGCCTCTCAAGTAGCTGGGACCATAGGT T G FAM222B Ensembl:ENSG00000173065 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1200053688 Functional Loss SNV dbSNP153 33..33 33 - - - 6729 RMVar_ID_6729 Human_SNP_ID_621246419 A-to-I Human chr17 - 28827319 28827319 28827319 GATCTCACTGTGTTACCCAGGCTTGGAGTGCCATGGCACTGTCATAGCTCACTGCAGCTTCTAAA GATCTCACTGTGTTACCCAGGCTTGGAGTGCCGTGGCACTGTCATAGCTCACTGCAGCTTCTAAA T C FAM222B Ensembl:ENSG00000173065 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs558695732 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12942242 6730 RMVar_ID_6730 Human_SNP_ID_621246426 A-to-I Human chr17 - 28827352 28827352 28827352 TTTTTCACTTTTTCTTTTTTTTTCAATAGACAAGATCTCACTGTGTTACCCAGGCTTGGAGTGCC TTTTTCACTTTTTCTTTTTTTTTCAATAGACAGGATCTCACTGTGTTACCCAGGCTTGGAGTGCC T C FAM222B Ensembl:ENSG00000173065 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs918638428 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6573847,Human_RBP_ID_12942242,Human_RBP_ID_23167824 6731 RMVar_ID_6731 Human_SNP_ID_621247007 A-to-I Human chr17 - 28829408 28829408 28829408 CAGCACTTTGGGAGGCCGAGTTGGGGCGGATCACCTGAGGTCGGGAGTTTGAGACCAGCCTGAGC CAGCACTTTGGGAGGCCGAGTTGGGGCGGATCTCCTGAGGTCGGGAGTTTGAGACCAGCCTGAGC T A FAM222B Ensembl:ENSG00000173065 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1018056290 Functional Loss SNV dbSNP153 33..33 33 - - - 6732 RMVar_ID_6732 Human_SNP_ID_621247008 A-to-I Human chr17 - 28829408 28829408 28829408 CAGCACTTTGGGAGGCCGAGTTGGGGCGGATCACCTGAGGTCGGGAGTTTGAGACCAGCCTGAGC CAGCACTTTGGGAGGCCGAGTTGGGGCGGATCCCCTGAGGTCGGGAGTTTGAGACCAGCCTGAGC T G FAM222B Ensembl:ENSG00000173065 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1018056290 Functional Loss SNV dbSNP153 33..33 33 - - - 6733 RMVar_ID_6733 Human_SNP_ID_621247171 A-to-I Human chr17 - 28829988 28829988 28829988 AAAATTAGCCAGGCATGGTGGCTTGCGCCTGTAGTCCCGGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTAGCCAGGCATGGTGGCTTGCGCCTGTTGTCCCGGCTACTCGGGAGGCTGAGGCAGGAGA T A FAM222B Ensembl:ENSG00000173065 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1014362005 Functional Loss SNV dbSNP153 33..33 33 - - - 6734 RMVar_ID_6734 Human_SNP_ID_621247979 A-to-I Human chr17 - 28833088 28833088 28833088 TCGAACTCCTGACCTTGTTATCCGCCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCCTGAG TCGAACTCCTGACCTTGTTATCCGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCCTGAG T C FAM222B Ensembl:ENSG00000173065 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049635119 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12942339 6735 RMVar_ID_6735 Human_SNP_ID_621248724 A-to-I Human chr17 - 28835812 28835812 28835812 AAAAAATGAGCCGGGTGTGGTGGCATGCACCTATAGTCCCAGGTACTTGGGAGGCTGAGGTGGGA AAAAAATGAGCCGGGTGTGGTGGCATGCACCTGTAGTCCCAGGTACTTGGGAGGCTGAGGTGGGA T C FAM222B Ensembl:ENSG00000173065 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1478105101 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183023 6736 RMVar_ID_6736 Human_SNP_ID_621249360 A-to-I Human chr17 - 28838047 28838047 28838047 TGGCCAGTCTGGTCTCGAACTCCTGACCTCAAATGTTCCACCCGCCTCTACCTCCCAAAGTGCTG TGGCCAGTCTGGTCTCGAACTCCTGACCTCAAGTGTTCCACCCGCCTCTACCTCCCAAAGTGCTG T C FAM222B Ensembl:ENSG00000173065 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1014320447 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12942444 6737 RMVar_ID_6737 Human_SNP_ID_621249425 A-to-I Human chr17 - 28838277 28838277 28838277 CGCGCCCGGCCTATTTGTTGTTTTTTTGAGACAGGGTCTCACTCTGTCGCCCAGACTGGAGTGCA CGCGCCCGGCCTATTTGTTGTTTTTTTGAGACGGGGTCTCACTCTGTCGCCCAGACTGGAGTGCA T C FAM222B Ensembl:ENSG00000173065 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1413667726 Functional Loss SNV dbSNP153 33..33 33 - - - 6738 RMVar_ID_6738 Human_SNP_ID_621249445 A-to-I Human chr17 - 28838324 28838324 28838324 TGCCTACCTCGGCCTCCCAAAGTGTTGGGATTACAGGCGTGAGCCACCGCGCCCGGCCTATTTGT TGCCTACCTCGGCCTCCCAAAGTGTTGGGATTGCAGGCGTGAGCCACCGCGCCCGGCCTATTTGT T C FAM222B Ensembl:ENSG00000173065 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1198116156 Functional Loss SNV dbSNP153 33..33 33 - - - 6739 RMVar_ID_6739 Human_SNP_ID_621249642 A-to-I Human chr17 - 28839095 28839095 28839095 TCTCGCCATTCTCCTGCCTCAGCCTCCCTAGTAGCTGGAACTACAGGCACCCGCCACCATGCCTG TCTCGCCATTCTCCTGCCTCAGCCTCCCTAGTGGCTGGAACTACAGGCACCCGCCACCATGCCTG T C FAM222B Ensembl:ENSG00000173065 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs915370057 Functional Loss SNV dbSNP153 33..33 33 - - - 6740 RMVar_ID_6740 Human_SNP_ID_621250068 A-to-I Human chr17 - 28840839 28840839 28840839 CTCCTGCCTCAGCCTCCCTAGTACCTGGGATTATAGGCACGTGCCACCATACCCGGCTAATTTTT CTCCTGCCTCAGCCTCCCTAGTACCTGGGATTGTAGGCACGTGCCACCATACCCGGCTAATTTTT T C FAM222B Ensembl:ENSG00000173065 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1451008829 Functional Loss SNV dbSNP153 33..33 33 - - - 6741 RMVar_ID_6741 Human_SNP_ID_621254519 A-to-I Human chr17 + 28856805 28856805 28856805 GCGATCTTGGCTCACTGCAAGCTCCACCTCCCAGGTTGACGCCATTCTCCTGCCTCAGCCTCCTG GCGATCTTGGCTCACTGCAAGCTCCACCTCCCCGGTTGACGCCATTCTCCTGCCTCAGCCTCCTG A C ERAL1 Ensembl:ENSG00000132591 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs867914685 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91655,RMVar_hsa_circ_94475,RMVar_hsa_circ_183024,RMVar_hsa_circ_183025 6742 RMVar_ID_6742 Human_SNP_ID_621254736 A-to-I Human chr17 + 28857638 28857638 28857638 ATGGTGAAACCCTGTCTCTACTAAAAAAATACAAAAATTAGCCGGGTGTGGTGGTGCACGCCTGT ATGGTGAAACCCTGTCTCTACTAAAAAAATACGAAAATTAGCCGGGTGTGGTGGTGCACGCCTGT A G ERAL1 Ensembl:ENSG00000132591 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1263308168 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91655,RMVar_hsa_circ_94475,RMVar_hsa_circ_183024,RMVar_hsa_circ_183025 6743 RMVar_ID_6743 Human_SNP_ID_621260114 A-to-I Human chr17 - 28879528 28879528 28879528 ATCCTCTGTCTCCTTGCTCCAATGGAGGCAGAAGAGCCCAGGACCCAAGCGTCTTGGCAGGGGTG ATCCTCTGTCTCCTTGCTCCAATGGAGGCAGAGGAGCCCAGGACCCAAGCGTCTTGGCAGGGGTG T C FLOT2 Ensembl:ENSG00000132589 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1321756081 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_486017,Human_RBP_ID_20194419,Human_RBP_ID_26448539 Human_miRNA_ID_2041081,Human_miRNA_ID_2554836,Human_miRNA_ID_3020065 RMVar_hsa_circ_89777,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_183037,RMVar_hsa_circ_183034,RMVar_hsa_circ_183031,RMVar_hsa_circ_183032 6744 RMVar_ID_6744 Human_SNP_ID_621273778 A-to-I Human chr17 - 28932320 28932320 28932320 AGACCCAGCCTTCGGCAACATAGTGAAACCCTATTTCTACAAAAAATATAAAATTTAGCCCAGCG AGACCCAGCCTTCGGCAACATAGTGAAACCCTGTTTCTACAAAAAATATAAAATTTAGCCCAGCG T C PHF12 Ensembl:ENSG00000109118 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984534841 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90398,RMVar_hsa_circ_183047,RMVar_hsa_circ_97720,RMVar_hsa_circ_183056 6745 RMVar_ID_6745 Human_SNP_ID_621273867 A-to-I Human chr17 - 28932846 28932846 28932846 CACCTCCTGGGTTCAAGCAATTCTCTTGCCTCAGCTTCCCCAGTAGCTGGGACTACAAGTGCACA CACCTCCTGGGTTCAAGCAATTCTCTTGCCTCGGCTTCCCCAGTAGCTGGGACTACAAGTGCACA T C PHF12 Ensembl:ENSG00000109118 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1355534708 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90398,RMVar_hsa_circ_183047,RMVar_hsa_circ_97720,RMVar_hsa_circ_183056 6746 RMVar_ID_6746 Human_SNP_ID_621273869 A-to-I Human chr17 - 28932859 28932859 28932859 TCACTGCAACCTCCACCTCCTGGGTTCAAGCAATTCTCTTGCCTCAGCTTCCCCAGTAGCTGGGA TCACTGCAACCTCCACCTCCTGGGTTCAAGCAGTTCTCTTGCCTCAGCTTCCCCAGTAGCTGGGA T C PHF12 Ensembl:ENSG00000109118 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1235089115 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90398,RMVar_hsa_circ_183047,RMVar_hsa_circ_97720,RMVar_hsa_circ_183056 6747 RMVar_ID_6747 Human_SNP_ID_621274088 A-to-I Human chr17 - 28933865 28933865 28933865 TTTTTGTATTTTTGTAGAAATGGGGTCTCACCATGTTGCCCAGCCTGGCCTCTAACTCCTGGGGT TTTTTGTATTTTTGTAGAAATGGGGTCTCACCGTGTTGCCCAGCCTGGCCTCTAACTCCTGGGGT T C PHF12 Ensembl:ENSG00000109118 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs755399813 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90398,RMVar_hsa_circ_183047,RMVar_hsa_circ_97720,RMVar_hsa_circ_183056 6748 RMVar_ID_6748 Human_SNP_ID_621274455 A-to-I Human chr17 - 28935410 28935410 28935410 AAAATTAGCCCAGTGTGGTGGTGCATGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCACAACA AAAATTAGCCCAGTGTGGTGGTGCATGCCTGTGATCCCAGCTACTCAGGAGGCTGAGGCACAACA T C PHF12 Ensembl:ENSG00000109118 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs144847460 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90398,RMVar_hsa_circ_183047,RMVar_hsa_circ_97720,RMVar_hsa_circ_183056 6749 RMVar_ID_6749 Human_SNP_ID_621276932 A-to-I Human chr17 - 28946829 28946829 28946829 CGGAAAGTACAAGAGTAAGGTTGAAGCCGAGTATGGTGGCTCATGCCTGTAATCCCAGCACTTAA CGGAAAGTACAAGAGTAAGGTTGAAGCCGAGTGTGGTGGCTCATGCCTGTAATCCCAGCACTTAA T C PHF12 Ensembl:ENSG00000109118 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1567973620 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12943619 RMVar_hsa_circ_90398,RMVar_hsa_circ_183047,RMVar_hsa_circ_97720,RMVar_hsa_circ_183056 6750 RMVar_ID_6750 Human_SNP_ID_621312181 A-to-I Human chr17 - 29088238 29088238 29088238 CATCCTGGCTAACACGGTGAAACCCTGTCTCTACTAAAAATACAAAACATTAGCCGGGCGTGGTG CATCCTGGCTAACACGGTGAAACCCTGTCTCTGCTAAAAATACAAAACATTAGCCGGGCGTGGTG T C MYO18A Ensembl:ENSG00000196535 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs558660641 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_134523 RMVar_hsa_circ_59539,RMVar_hsa_circ_71390 6751 RMVar_ID_6751 Human_SNP_ID_621312196 A-to-I Human chr17 - 29088272 29088272 29088272 AGGTGGGCGGATCACGAGGTCAGGAGATCGAGACCATCCTGGCTAACACGGTGAAACCCTGTCTC AGGTGGGCGGATCACGAGGTCAGGAGATCGAGGCCATCCTGGCTAACACGGTGAAACCCTGTCTC T C MYO18A Ensembl:ENSG00000196535 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs892216972 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_134523 RMVar_hsa_circ_59539,RMVar_hsa_circ_71390 6752 RMVar_ID_6752 Human_SNP_ID_621312197 A-to-I Human chr17 - 29088272 29088272 29088272 AGGTGGGCGGATCACGAGGTCAGGAGATCGAGACCATCCTGGCTAACACGGTGAAACCCTGTCTC AGGTGGGCGGATCACGAGGTCAGGAGATCGAGCCCATCCTGGCTAACACGGTGAAACCCTGTCTC T G MYO18A Ensembl:ENSG00000196535 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs892216972 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_134523 RMVar_hsa_circ_59539,RMVar_hsa_circ_71390 6753 RMVar_ID_6753 Human_SNP_ID_621334229 A-to-I Human chr17 - 29175636 29175636 29175636 TAGTAGGCCGGACACAGTGGTTCACACCTGTAATCCCAGGACTTTGGGAGGCTGAGATAGGCAGA TAGTAGGCCGGACACAGTGGTTCACACCTGTAGTCCCAGGACTTTGGGAGGCTGAGATAGGCAGA T C MYO18A Ensembl:ENSG00000196535 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs990271558 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17565816 RMVar_hsa_circ_98280,RMVar_hsa_circ_183075 6754 RMVar_ID_6754 Human_SNP_ID_621334336 A-to-I Human chr17 - 29176053 29176051 29176054 CGAATTTTTCCAGACTGCTGTTTTTTTTGAGAAGGAGTCTCGCTCTGTCACCCAGGCTGGAGTGC CGAATTTTTCCAGACTGCTGTTTTTTTTGAG___GAGTCTCGCTCTGTCACCCAGGCTGGAGTGC CCTT C MYO18A Ensembl:ENSG00000196535 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs918441114 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_98280,RMVar_hsa_circ_183075 6755 RMVar_ID_6755 Human_SNP_ID_621334337 A-to-I Human chr17 - 29176053 29176053 29176053 CGAATTTTTCCAGACTGCTGTTTTTTTTGAGAAGGAGTCTCGCTCTGTCACCCAGGCTGGAGTGC CGAATTTTTCCAGACTGCTGTTTTTTTTGAGAGGGAGTCTCGCTCTGTCACCCAGGCTGGAGTGC T C MYO18A Ensembl:ENSG00000196535 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1376312080 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98280,RMVar_hsa_circ_183075 6756 RMVar_ID_6756 Human_SNP_ID_621357437 A-to-I Human chr17 - 29271296 29271296 29271296 CTTACCTCGTGATCCACCTGCCTCGGCCTCCCAAAGTGCTGAGATTACAGATGTGAGCCCCTCCG CTTACCTCGTGATCCACCTGCCTCGGCCTCCCGAAGTGCTGAGATTACAGATGTGAGCCCCTCCG T C NUFIP2 Ensembl:ENSG00000108256 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1345023428 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_365370 6757 RMVar_ID_6757 Human_SNP_ID_621357483 A-to-I Human chr17 - 29271454 29271454 29271454 CGGCTCACTGCAACCTCCGTCTACGGGGTTCAAGTGATTCTCCTGCCTTAGCCTGCTCAGTAGCT CGGCTCACTGCAACCTCCGTCTACGGGGTTCATGTGATTCTCCTGCCTTAGCCTGCTCAGTAGCT T A NUFIP2 Ensembl:ENSG00000108256 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1567676909 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_365370 6758 RMVar_ID_6758 Human_SNP_ID_621357616 A-to-I Human chr17 - 29271888 29271888 29271888 TTTTGTGTTTTTAGTAGAGATGGGATTTCACCATGTTGGTCAGGCTGGTCTTGAACTCCTGACCT TTTTGTGTTTTTAGTAGAGATGGGATTTCACCGTGTTGGTCAGGCTGGTCTTGAACTCCTGACCT T C NUFIP2 Ensembl:ENSG00000108256 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1012069616 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_365370 6759 RMVar_ID_6759 Human_SNP_ID_621357638 A-to-I Human chr17 - 29271951 29271951 29271951 CTCCTGTCTCAGCCTCCTGAGTAGCTAGGACTACCGGTGCCCGCCCCCACACTTGGCTAACTTTT CTCCTGTCTCAGCCTCCTGAGTAGCTAGGACTGCCGGTGCCCGCCCCCACACTTGGCTAACTTTT T C NUFIP2 Ensembl:ENSG00000108256 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1319161510 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12944843 RMVar_hsa_circ_365370 6760 RMVar_ID_6760 Human_SNP_ID_621357824 A-to-I Human chr17 - 29272379 29272376 29272379 GAAATTAGCCGGGCTTGGTGGCATGCGCCTGTAGTCTCAGCTATTCGGGAGGCTGAGGCGGGAGA GAAATTAGCCGGGCTTGGTGGCATGCGCCTGT___CTCAGCTATTCGGGAGGCTGAGGCGGGAGA GACT G NUFIP2 Ensembl:ENSG00000108256 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1237239426 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_365370 6761 RMVar_ID_6761 Human_SNP_ID_621358031 A-to-I Human chr17 - 29272913 29272913 29272913 AGGTGGTGGAGGTTGCAGTGAGCTGAGATCGCACCACTGCTGCTCTTCAGCCTGGGCGACAGCAA AGGTGGTGGAGGTTGCAGTGAGCTGAGATCGCGCCACTGCTGCTCTTCAGCCTGGGCGACAGCAA T C NUFIP2 Ensembl:ENSG00000108256 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs923332052 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9850799,Human_RBP_ID_12944855 RMVar_hsa_circ_365370 6762 RMVar_ID_6762 Human_SNP_ID_621358675 A-to-I Human chr17 - 29275115 29275090 29275115 TTGGGGGGGGCTGAGGCAGGAGAATTGCCTGAAGCCAGGAGGTGGAGGTTGCAGTGAGCCGAGAT TTGGGGGGGGCTGAGGCAGGAGAATTGCCTGA_________________________GCCGAGAT CTCACTGCAACCTCCACCTCCTGGCT C NUFIP2 Ensembl:ENSG00000108256 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1374911731 Functional Loss DEL dbSNP153 33..57 33 - - - RMVar_hsa_circ_365370 6763 RMVar_ID_6763 Human_SNP_ID_621358679 A-to-I Human chr17 - 29275111 29275111 29275111 GGGGGGCTGAGGCAGGAGAATTGCCTGAAGCCAGGAGGTGGAGGTTGCAGTGAGCCGAGATCGAG GGGGGGCTGAGGCAGGAGAATTGCCTGAAGCCGGGAGGTGGAGGTTGCAGTGAGCCGAGATCGAG T C NUFIP2 Ensembl:ENSG00000108256 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1348495642 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_365370 6764 RMVar_ID_6764 Human_SNP_ID_621359091 A-to-I Human chr17 - 29276449 29276449 29276449 GCGTGCCTGTAGTCCCAGCTACTCAGGAGACTAAGGCAGGAGAATCGCTTGAACCTGGGAGGTGG GCGTGCCTGTAGTCCCAGCTACTCAGGAGACTTAGGCAGGAGAATCGCTTGAACCTGGGAGGTGG T A NUFIP2 Ensembl:ENSG00000108256 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1375337007 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_365370 6765 RMVar_ID_6765 Human_SNP_ID_621359097 A-to-I Human chr17 - 29276461 29276461 29276461 AGGCATGGTGGCGCGTGCCTGTAGTCCCAGCTACTCAGGAGACTAAGGCAGGAGAATCGCTTGAA AGGCATGGTGGCGCGTGCCTGTAGTCCCAGCTGCTCAGGAGACTAAGGCAGGAGAATCGCTTGAA T C NUFIP2 Ensembl:ENSG00000108256 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs916043067 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_365370 6766 RMVar_ID_6766 Human_SNP_ID_621359109 A-to-I Human chr17 - 29276493 29276493 29276493 ATCTCTCCTAAAACAATATACAAAAATTAGCCAGGCATGGTGGCGCGTGCCTGTAGTCCCAGCTA ATCTCTCCTAAAACAATATACAAAAATTAGCCGGGCATGGTGGCGCGTGCCTGTAGTCCCAGCTA T C NUFIP2 Ensembl:ENSG00000108256 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1485298534 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12944957 RMVar_hsa_circ_365370 6767 RMVar_ID_6767 Human_SNP_ID_621359275 A-to-I Human chr17 - 29277198 29277198 29277198 CAGTGTGGTGAAACCCGGTCTCTACTAAAAATACAAAAATGAGCCGGGCATGGTGGCACGTGCCT CAGTGTGGTGAAACCCGGTCTCTACTAAAAATTCAAAAATGAGCCGGGCATGGTGGCACGTGCCT T A NUFIP2 Ensembl:ENSG00000108256 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1305859309 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_365370 6768 RMVar_ID_6768 Human_SNP_ID_621359289 A-to-I Human chr17 - 29277267 29277267 29277267 AAATCCCAGCATTTTAGGAGGCTGAGGTGGGCAGATCCCCTGAGGTCAGGAGTTCGAGACCAGCC AAATCCCAGCATTTTAGGAGGCTGAGGTGGGCGGATCCCCTGAGGTCAGGAGTTCGAGACCAGCC T C NUFIP2 Ensembl:ENSG00000108256 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs978610011 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_365370 6769 RMVar_ID_6769 Human_SNP_ID_621359409 A-to-I Human chr17 - 29277830 29277830 29277830 TTTGTATTTTTAGTAGAGACTGAGGTTTCACCATGTTGGTCAGGCTGGTCTCAAACTCCTGACCT TTTGTATTTTTAGTAGAGACTGAGGTTTCACCGTGTTGGTCAGGCTGGTCTCAAACTCCTGACCT T C NUFIP2 Ensembl:ENSG00000108256 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223476494 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_365370 6770 RMVar_ID_6770 Human_SNP_ID_621359946 A-to-I Human chr17 - 29279625 29279625 29279625 GGAGGCTGAGATGGAGGATATCACCAAGCCCAAGAGGTCAAAGATGCAGTGAGCCATAATCGTGC GGAGGCTGAGATGGAGGATATCACCAAGCCCATGAGGTCAAAGATGCAGTGAGCCATAATCGTGC T A NUFIP2 Ensembl:ENSG00000108256 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1003795780 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17565547 RMVar_hsa_circ_365370 6771 RMVar_ID_6771 Human_SNP_ID_621360005 A-to-I Human chr17 - 29279857 29279857 29279857 CTGAGATCACACCACTGCACTCTATCCAGCCTAGGAGACACAGCAAGACTTCACCTCAAAAAATG CTGAGATCACACCACTGCACTCTATCCAGCCTGGGAGACACAGCAAGACTTCACCTCAAAAAATG T C NUFIP2 Ensembl:ENSG00000108256 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs764823081 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12945074 RMVar_hsa_circ_365370 6772 RMVar_ID_6772 Human_SNP_ID_621360021 A-to-I Human chr17 - 29279901 29279901 29279901 GGTGGGAGAATCGCTTGAATCTGGGAGGTGGAAGTTGCAGTGGGCTGAGATCACACCACTGCACT GGTGGGAGAATCGCTTGAATCTGGGAGGTGGAGGTTGCAGTGGGCTGAGATCACACCACTGCACT T C NUFIP2 Ensembl:ENSG00000108256 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1414453217 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17565817 RMVar_hsa_circ_365370 6773 RMVar_ID_6773 Human_SNP_ID_621360073 A-to-I Human chr17 - 29280097 29280097 29280097 TTAAAAATAGGCTGGGGCCGGACATGGCTCACACTTGTAATCCCAGCACGTTGGGAGGCTGAGGC TTAAAAATAGGCTGGGGCCGGACATGGCTCACGCTTGTAATCCCAGCACGTTGGGAGGCTGAGGC T C NUFIP2 Ensembl:ENSG00000108256 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017061850 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_365370 6774 RMVar_ID_6774 Human_SNP_ID_621360200 A-to-I Human chr17 - 29280642 29280642 29280642 TCACCCTGTGACTCAGGCTGGAATGCAGTGGTATGATCCTAGCTCACTGCACCCTTGAACTCCTG TCACCCTGTGACTCAGGCTGGAATGCAGTGGTGTGATCCTAGCTCACTGCACCCTTGAACTCCTG T C NUFIP2 Ensembl:ENSG00000108256 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1359190001 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12945097,Human_RBP_ID_17565818 RMVar_hsa_circ_365370 6775 RMVar_ID_6775 Human_SNP_ID_621360225 A-to-I Human chr17 - 29280768 29280768 29280768 TTGGCCAGACTGGTCTTGAACTCTTGACCTCAAGTTCTCCGCCCACCTCCGCCTCCGAAAGTGCT TTGGCCAGACTGGTCTTGAACTCTTGACCTCAGGTTCTCCGCCCACCTCCGCCTCCGAAAGTGCT T C NUFIP2 Ensembl:ENSG00000108256 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs918859738 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12945098,Human_RBP_ID_22717393 RMVar_hsa_circ_365370 6776 RMVar_ID_6776 Human_SNP_ID_621360229 A-to-I Human chr17 - 29280794 29280794 29280794 TTTAGTAGAGACGGGGTTTCGCCATGTTGGCCAGACTGGTCTTGAACTCTTGACCTCAAGTTCTC TTTAGTAGAGACGGGGTTTCGCCATGTTGGCCGGACTGGTCTTGAACTCTTGACCTCAAGTTCTC T C NUFIP2 Ensembl:ENSG00000108256 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1253963186 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12945098 RMVar_hsa_circ_365370 6777 RMVar_ID_6777 Human_SNP_ID_621360645 A-to-I Human chr17 - 29282043 29282043 29282043 AAAAAGGGGATTTGTGCTGGGTGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAG AAAAAGGGGATTTGTGCTGGGTGCGGTGGCTCGCGCCTGTAATCCCAGCACTTTGGGAGGCCAAG T C NUFIP2 Ensembl:ENSG00000108256 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1047512235 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_365370 6778 RMVar_ID_6778 Human_SNP_ID_621360720 A-to-I Human chr17 - 29282312 29282312 29282312 GACCTCATGAGCCACCTGCCTTGGCCTCCCAAAGTGCTGGGATTACGGGTGTGAGCCACTGCACC GACCTCATGAGCCACCTGCCTTGGCCTCCCAACGTGCTGGGATTACGGGTGTGAGCCACTGCACC T G NUFIP2 Ensembl:ENSG00000108256 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1482836711 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9850895,Human_RBP_ID_17565819 RMVar_hsa_circ_365370 6779 RMVar_ID_6779 Human_SNP_ID_621361006 A-to-I Human chr17 - 29283441 29283441 29283441 CCAGCTACTTGGGAGGCTTAGGAGGGAGGATCACTTGTCCCTGGGAGATCCAGGTCTGCAGTGAG CCAGCTACTTGGGAGGCTTAGGAGGGAGGATCTCTTGTCCCTGGGAGATCCAGGTCTGCAGTGAG T A NUFIP2 Ensembl:ENSG00000108256 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1423932882 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17565549 RMVar_hsa_circ_365370 6780 RMVar_ID_6780 Human_SNP_ID_621361007 A-to-I Human chr17 - 29283441 29283441 29283441 CCAGCTACTTGGGAGGCTTAGGAGGGAGGATCACTTGTCCCTGGGAGATCCAGGTCTGCAGTGAG CCAGCTACTTGGGAGGCTTAGGAGGGAGGATCGCTTGTCCCTGGGAGATCCAGGTCTGCAGTGAG T C NUFIP2 Ensembl:ENSG00000108256 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1423932882 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17565549 RMVar_hsa_circ_365370 6781 RMVar_ID_6781 Human_SNP_ID_621362507 A-to-I Human chr17 - 29288107 29288107 29288107 CCCGGGAGGTGGAGCTTACAGTGAGCGGAGATAGCGCCACTGCACTCCAGCCTGGGCGACAGAGT CCCGGGAGGTGGAGCTTACAGTGAGCGGAGATCGCGCCACTGCACTCCAGCCTGGGCGACAGAGT T G NUFIP2 Ensembl:ENSG00000108256 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs892839266 Functional Loss SNV dbSNP153 33..33 33 - - - 6782 RMVar_ID_6782 Human_SNP_ID_621362722 A-to-I Human chr17 - 29288987 29288987 29288987 AGGCACATGCCCCACGCCCAGCTAATTTTTGTATTTGTAGTAGAGACAGGGTTTCTCCATGTTGC AGGCACATGCCCCACGCCCAGCTAATTTTTGTGTTTGTAGTAGAGACAGGGTTTCTCCATGTTGC T C NUFIP2 Ensembl:ENSG00000108256 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1299707145 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12945440 6783 RMVar_ID_6783 Human_SNP_ID_621362753 A-to-I Human chr17 - 29289124 29289124 29289124 CTTTTCTTCTTGAAAGAGGGTCTCACTTTGTCACTCAAGCTAGAAGGCAGTTGTGCCATCTCAGT CTTTTCTTCTTGAAAGAGGGTCTCACTTTGTCGCTCAAGCTAGAAGGCAGTTGTGCCATCTCAGT T C NUFIP2 Ensembl:ENSG00000108256 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs749182010 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12945442 6784 RMVar_ID_6784 Human_SNP_ID_621362838 A-to-I Human chr17 - 29289480 29289480 29289480 TCAAGCCATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCGTGCACCACCATGCCTG TCAAGCCATTCTCCTGCCTCAGCCTCCCAAGTGGCTGGGATTACAGGCGTGCACCACCATGCCTG T C NUFIP2 Ensembl:ENSG00000108256 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs953791999 Functional Loss SNV dbSNP153 33..33 33 - - - 6785 RMVar_ID_6785 Human_SNP_ID_621363015 A-to-I Human chr17 - 29290102 29290102 29290102 GGCGGGCAGATCACTTGAGGTCAGGAGTTCGAAACCAGCCAGGCCAACGTGGCGGAACTGGGCAT GGCGGGCAGATCACTTGAGGTCAGGAGTTCGAGACCAGCCAGGCCAACGTGGCGGAACTGGGCAT T C NUFIP2 Ensembl:ENSG00000108256 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs921329203 Functional Loss SNV dbSNP153 33..33 33 - - - 6786 RMVar_ID_6786 Human_SNP_ID_621363022 A-to-I Human chr17 - 29290127 29290127 29290127 TAATCCCAGCACTTTGGGAGGCCCAGGCGGGCAGATCACTTGAGGTCAGGAGTTCGAAACCAGCC TAATCCCAGCACTTTGGGAGGCCCAGGCGGGCCGATCACTTGAGGTCAGGAGTTCGAAACCAGCC T G NUFIP2 Ensembl:ENSG00000108256 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs979138728 Functional Loss SNV dbSNP153 33..33 33 - - - 6787 RMVar_ID_6787 Human_SNP_ID_621390169 A-to-I Human chr17 + 29395737 29395737 29395737 TGGAATGCAATAGCGTGATCACAGCGTATTGCAGCCTCAGCCTCCCGGGTTCAAGTGCTCTTCCC TGGAATGCAATAGCGTGATCACAGCGTATTGCGGCCTCAGCCTCCCGGGTTCAAGTGCTCTTCCC A G AC068025.2,TAOK1 Ensembl:ENSG00000266111,Ensembl:ENSG00000160551 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs962674128 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12945788 RMVar_hsa_circ_95392,RMVar_hsa_circ_56294,RMVar_hsa_circ_183082,RMVar_hsa_circ_90691,RMVar_hsa_circ_183081 6788 RMVar_ID_6788 Human_SNP_ID_621391167 A-to-I Human chr17 + 29398121 29398120 29398121 ACTCATGGGGGCTCAGGCAGTCCTCCCTCCTCAGCATCCCAAAGAGCTGGGATTACAGGCATGAG ACTCATGGGGGCTCAGGCAGTCCTCCCTCCTC_GCATCCCAAAGAGCTGGGATTACAGGCATGAG CA C AC068025.2,TAOK1 Ensembl:ENSG00000266111,Ensembl:ENSG00000160551 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1203936601 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5248344,Human_RBP_ID_17566408 RMVar_hsa_circ_95392,RMVar_hsa_circ_56294,RMVar_hsa_circ_183082,RMVar_hsa_circ_90691,RMVar_hsa_circ_183081 6789 RMVar_ID_6789 Human_SNP_ID_621391231 A-to-I Human chr17 + 29398345 29398345 29398345 TCTCCTGCCTCAGCCTCCCAACAGCTGGGATTACAGGTATGCGCCACCATGCCCAGCTAATTTTT TCTCCTGCCTCAGCCTCCCAACAGCTGGGATTCCAGGTATGCGCCACCATGCCCAGCTAATTTTT A C AC068025.2,TAOK1 Ensembl:ENSG00000266111,Ensembl:ENSG00000160551 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1050419787 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95392,RMVar_hsa_circ_56294,RMVar_hsa_circ_183082,RMVar_hsa_circ_90691,RMVar_hsa_circ_183081 6790 RMVar_ID_6790 Human_SNP_ID_621391233 A-to-I Human chr17 + 29398351 29398351 29398351 GCCTCAGCCTCCCAACAGCTGGGATTACAGGTATGCGCCACCATGCCCAGCTAATTTTTTGTATT GCCTCAGCCTCCCAACAGCTGGGATTACAGGTGTGCGCCACCATGCCCAGCTAATTTTTTGTATT A G AC068025.2,TAOK1 Ensembl:ENSG00000266111,Ensembl:ENSG00000160551 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1228454821 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95392,RMVar_hsa_circ_56294,RMVar_hsa_circ_183082,RMVar_hsa_circ_90691,RMVar_hsa_circ_183081 6791 RMVar_ID_6791 Human_SNP_ID_621391635 A-to-I Human chr17 + 29399863 29399863 29399863 GCGATCCTCTCACCTCAGCCACCTCAGCAGCTAGGACTACAGGCGTGCACCACCACACCTGGCTA GCGATCCTCTCACCTCAGCCACCTCAGCAGCTGGGACTACAGGCGTGCACCACCACACCTGGCTA A G AC068025.2,TAOK1 Ensembl:ENSG00000266111,Ensembl:ENSG00000160551 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971822620 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95392,RMVar_hsa_circ_56294,RMVar_hsa_circ_183082,RMVar_hsa_circ_90691,RMVar_hsa_circ_183081 6792 RMVar_ID_6792 Human_SNP_ID_621392280 A-to-I Human chr17 + 29402321 29402320 29402321 TAAAAAAAGAAGACTTTCTATTTAATTTTTTTAAGACGGTCTCAGTCCCCTTCCCTATGCTAGAG TAAAAAAAGAAGACTTTCTATTTAATTTTTTT_AGACGGTCTCAGTCCCCTTCCCTATGCTAGAG TA T AC068025.2,TAOK1 Ensembl:ENSG00000266111,Ensembl:ENSG00000160551 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1478904230 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_6575260,Human_RBP_ID_12945945,Human_RBP_ID_23718622 RMVar_hsa_circ_95392,RMVar_hsa_circ_56294,RMVar_hsa_circ_183082,RMVar_hsa_circ_90691,RMVar_hsa_circ_183081 6793 RMVar_ID_6793 Human_SNP_ID_621392281 A-to-I Human chr17 + 29402321 29402321 29402321 TAAAAAAAGAAGACTTTCTATTTAATTTTTTTAAGACGGTCTCAGTCCCCTTCCCTATGCTAGAG TAAAAAAAGAAGACTTTCTATTTAATTTTTTTGAGACGGTCTCAGTCCCCTTCCCTATGCTAGAG A G AC068025.2,TAOK1 Ensembl:ENSG00000266111,Ensembl:ENSG00000160551 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs868142803 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6575260,Human_RBP_ID_12945945,Human_RBP_ID_23718622 RMVar_hsa_circ_95392,RMVar_hsa_circ_56294,RMVar_hsa_circ_183082,RMVar_hsa_circ_90691,RMVar_hsa_circ_183081 6794 RMVar_ID_6794 Human_SNP_ID_621392312 A-to-I Human chr17 + 29402442 29402442 29402442 CTTTTACCTCAGCCTACCAAGTAGCTGAGACTACAGTCATGCGCCACCATACCTGACTAATTCTT CTTTTACCTCAGCCTACCAAGTAGCTGAGACTGCAGTCATGCGCCACCATACCTGACTAATTCTT A G AC068025.2,TAOK1 Ensembl:ENSG00000266111,Ensembl:ENSG00000160551 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1020871315 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95392,RMVar_hsa_circ_56294,RMVar_hsa_circ_183082,RMVar_hsa_circ_90691,RMVar_hsa_circ_183081 6795 RMVar_ID_6795 Human_SNP_ID_621392765 A-to-I Human chr17 + 29404296 29404296 29404296 GTGATCCTCCTGCCTCAGCCCCACAAGTAGCTAGGACTACAGCCCTGTGCTACCACACCCAGCGA GTGATCCTCCTGCCTCAGCCCCACAAGTAGCTGGGACTACAGCCCTGTGCTACCACACCCAGCGA A G TAOK1 Ensembl:ENSG00000160551 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1458575006 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12945995 RMVar_hsa_circ_95392,RMVar_hsa_circ_56294,RMVar_hsa_circ_183082,RMVar_hsa_circ_90691,RMVar_hsa_circ_183081 6796 RMVar_ID_6796 Human_SNP_ID_621392839 A-to-I Human chr17 + 29404647 29404647 29404647 GCCTCATCTCTACTAAAAATAAAAAATTAGCCAAGTACGGTGGCATGTGCCTGTGGTCCCAGCTA GCCTCATCTCTACTAAAAATAAAAAATTAGCCTAGTACGGTGGCATGTGCCTGTGGTCCCAGCTA A T TAOK1 Ensembl:ENSG00000160551 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1567708820 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12945998 RMVar_hsa_circ_95392,RMVar_hsa_circ_56294,RMVar_hsa_circ_183082,RMVar_hsa_circ_90691,RMVar_hsa_circ_183081 6797 RMVar_ID_6797 Human_SNP_ID_621392855 A-to-I Human chr17 + 29404729 29404729 29404729 GGAGGATTGCTGGAACCTAGGAGGATGGAGTTACAGTGAGCCATGGTTGTGCTACTGCATTCCAG GGAGGATTGCTGGAACCTAGGAGGATGGAGTTGCAGTGAGCCATGGTTGTGCTACTGCATTCCAG A G TAOK1 Ensembl:ENSG00000160551 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1400045884 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95392,RMVar_hsa_circ_56294,RMVar_hsa_circ_183082,RMVar_hsa_circ_90691,RMVar_hsa_circ_183081 6798 RMVar_ID_6798 Human_SNP_ID_621393268 A-to-I Human chr17 + 29406577 29406577 29406577 TGAGACTGGATCTCACTGTTTTGCCCAGACTGAAGTGCAATGGCACAATCACGGCTCACTGTAGC TGAGACTGGATCTCACTGTTTTGCCCAGACTGGAGTGCAATGGCACAATCACGGCTCACTGTAGC A G TAOK1 Ensembl:ENSG00000160551 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7208552 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95392,RMVar_hsa_circ_56294,RMVar_hsa_circ_183082,RMVar_hsa_circ_90691,RMVar_hsa_circ_183081 6799 RMVar_ID_6799 Human_SNP_ID_621393269 A-to-I Human chr17 + 29406577 29406577 29406577 TGAGACTGGATCTCACTGTTTTGCCCAGACTGAAGTGCAATGGCACAATCACGGCTCACTGTAGC TGAGACTGGATCTCACTGTTTTGCCCAGACTGTAGTGCAATGGCACAATCACGGCTCACTGTAGC A T TAOK1 Ensembl:ENSG00000160551 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7208552 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95392,RMVar_hsa_circ_56294,RMVar_hsa_circ_183082,RMVar_hsa_circ_90691,RMVar_hsa_circ_183081 6800 RMVar_ID_6800 Human_SNP_ID_621393303 A-to-I Human chr17 + 29406716 29406716 29406716 ACCCACCCCCCCAACTAAGCAGCTGGGAGACTACTGGCATACACCACCATGGCCAGCTAATTTTT ACCCACCCCCCCAACTAAGCAGCTGGGAGACTCCTGGCATACACCACCATGGCCAGCTAATTTTT A C TAOK1 Ensembl:ENSG00000160551 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1216283715 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95392,RMVar_hsa_circ_56294,RMVar_hsa_circ_183082,RMVar_hsa_circ_90691,RMVar_hsa_circ_183081 6801 RMVar_ID_6801 Human_SNP_ID_621398307 A-to-I Human chr17 + 29425568 29425568 29425568 GAGTAAGGTGGTGTGTGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGTAGGAGGATGGCTTGAG GAGTAAGGTGGTGTGTGCCTGTAGTCCCAGCTGCTCGGGAGGCTGAGGTAGGAGGATGGCTTGAG A G TAOK1 Ensembl:ENSG00000160551 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251971648 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95392,RMVar_hsa_circ_56294,RMVar_hsa_circ_183082,RMVar_hsa_circ_90691,RMVar_hsa_circ_183081 6802 RMVar_ID_6802 Human_SNP_ID_621398862 A-to-I Human chr17 + 29427820 29427820 29427820 GTGGTGGTGGACGCCTGTAATCACAGCTGCTCAGGAGGTTGAGGCACGAGAATTGTTTGAATCCG GTGGTGGTGGACGCCTGTAATCACAGCTGCTCGGGAGGTTGAGGCACGAGAATTGTTTGAATCCG A G TAOK1 Ensembl:ENSG00000160551 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559200869 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12946619 RMVar_hsa_circ_95392,RMVar_hsa_circ_56294,RMVar_hsa_circ_183082,RMVar_hsa_circ_90691,RMVar_hsa_circ_183081 6803 RMVar_ID_6803 Human_SNP_ID_621409259 A-to-I Human chr17 + 29470913 29470913 29470913 GGAAGGCCGAGGCAGGCGGATCACTTGAGGTCAGGAGTTTGAGACCAGCCTGGCCAATGTGGTGG GGAAGGCCGAGGCAGGCGGATCACTTGAGGTCGGGAGTTTGAGACCAGCCTGGCCAATGTGGTGG A G TAOK1 Ensembl:ENSG00000160551 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs954082909 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95392,RMVar_hsa_circ_183084,RMVar_hsa_circ_183092,RMVar_hsa_circ_288142,RMVar_hsa_circ_300315,RMVar_hsa_circ_326091,RMVar_hsa_circ_183082,RMVar_hsa_circ_90691,RMVar_hsa_circ_183081,RMVar_hsa_circ_359090,RMVar_hsa_circ_372593,RMVar_hsa_circ_353842,RMVar_hsa_circ_311255,RMVar_hsa_circ_314930,RMVar_hsa_circ_302855,RMVar_hsa_circ_299506,RMVar_hsa_circ_299620,RMVar_hsa_circ_64065,RMVar_hsa_circ_183094,RMVar_hsa_circ_183095,RMVar_hsa_circ_183093,RMVar_hsa_circ_183088,RMVar_hsa_circ_183090,RMVar_hsa_circ_183091,RMVar_hsa_circ_183089,RMVar_hsa_circ_183086,RMVar_hsa_circ_183087,RMVar_hsa_circ_183085,RMVar_hsa_circ_5164,RMVar_hsa_circ_323110,RMVar_hsa_circ_373334,RMVar_hsa_circ_183083,RMVar_hsa_circ_183099,RMVar_hsa_circ_378504,RMVar_hsa_circ_350728,RMVar_hsa_circ_369044,RMVar_hsa_circ_337674,RMVar_hsa_circ_64997,RMVar_hsa_circ_314389,RMVar_hsa_circ_59612,RMVar_hsa_circ_183101,RMVar_hsa_circ_183103,RMVar_hsa_circ_4845,RMVar_hsa_circ_183102,RMVar_hsa_circ_183100 6804 RMVar_ID_6804 Human_SNP_ID_621409997 A-to-I Human chr17 + 29473531 29473531 29473531 GGTGGCAGGAGGAATGCTTGAACCCAGGAGGCAGAAGTTGTAGTGAGCCAAGATCATGCCACTGC GGTGGCAGGAGGAATGCTTGAACCCAGGAGGCGGAAGTTGTAGTGAGCCAAGATCATGCCACTGC A G TAOK1 Ensembl:ENSG00000160551 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs143590008 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_291 RMVar_hsa_circ_95392,RMVar_hsa_circ_183084,RMVar_hsa_circ_183092,RMVar_hsa_circ_288142,RMVar_hsa_circ_300315,RMVar_hsa_circ_326091,RMVar_hsa_circ_183082,RMVar_hsa_circ_90691,RMVar_hsa_circ_183081,RMVar_hsa_circ_359090,RMVar_hsa_circ_372593,RMVar_hsa_circ_353842,RMVar_hsa_circ_311255,RMVar_hsa_circ_314930,RMVar_hsa_circ_302855,RMVar_hsa_circ_299506,RMVar_hsa_circ_299620,RMVar_hsa_circ_64065,RMVar_hsa_circ_183094,RMVar_hsa_circ_183095,RMVar_hsa_circ_183093,RMVar_hsa_circ_183088,RMVar_hsa_circ_183090,RMVar_hsa_circ_183091,RMVar_hsa_circ_183089,RMVar_hsa_circ_183086,RMVar_hsa_circ_183087,RMVar_hsa_circ_183085,RMVar_hsa_circ_5164,RMVar_hsa_circ_323110,RMVar_hsa_circ_373334,RMVar_hsa_circ_183083,RMVar_hsa_circ_183099,RMVar_hsa_circ_378504,RMVar_hsa_circ_350728,RMVar_hsa_circ_369044,RMVar_hsa_circ_337674,RMVar_hsa_circ_64997,RMVar_hsa_circ_314389,RMVar_hsa_circ_59612,RMVar_hsa_circ_183101,RMVar_hsa_circ_183103,RMVar_hsa_circ_4845,RMVar_hsa_circ_183102,RMVar_hsa_circ_183100 6805 RMVar_ID_6805 Human_SNP_ID_621410438 A-to-I Human chr17 + 29475426 29475426 29475426 GATGAGCATGGTGGTGTGCGCCTGTAGACCCAAATACTTGGGAGGCTGAGGTGGGAGGATCACTT GATGAGCATGGTGGTGTGCGCCTGTAGACCCACATACTTGGGAGGCTGAGGTGGGAGGATCACTT A C TAOK1 Ensembl:ENSG00000160551 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1036444333 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95392,RMVar_hsa_circ_183084,RMVar_hsa_circ_183092,RMVar_hsa_circ_288142,RMVar_hsa_circ_300315,RMVar_hsa_circ_326091,RMVar_hsa_circ_183082,RMVar_hsa_circ_90691,RMVar_hsa_circ_183081,RMVar_hsa_circ_359090,RMVar_hsa_circ_372593,RMVar_hsa_circ_353842,RMVar_hsa_circ_311255,RMVar_hsa_circ_314930,RMVar_hsa_circ_302855,RMVar_hsa_circ_299506,RMVar_hsa_circ_299620,RMVar_hsa_circ_64065,RMVar_hsa_circ_183094,RMVar_hsa_circ_183095,RMVar_hsa_circ_183093,RMVar_hsa_circ_183088,RMVar_hsa_circ_183090,RMVar_hsa_circ_183091,RMVar_hsa_circ_183089,RMVar_hsa_circ_183086,RMVar_hsa_circ_183087,RMVar_hsa_circ_183085,RMVar_hsa_circ_5164,RMVar_hsa_circ_323110,RMVar_hsa_circ_373334,RMVar_hsa_circ_183083,RMVar_hsa_circ_183099,RMVar_hsa_circ_378504,RMVar_hsa_circ_350728,RMVar_hsa_circ_369044,RMVar_hsa_circ_337674,RMVar_hsa_circ_64997,RMVar_hsa_circ_314389,RMVar_hsa_circ_59612,RMVar_hsa_circ_183101,RMVar_hsa_circ_183103,RMVar_hsa_circ_4845,RMVar_hsa_circ_183102,RMVar_hsa_circ_183100 6806 RMVar_ID_6806 Human_SNP_ID_621419743 A-to-I Human chr17 + 29514564 29514564 29514564 TAATTTATTTTTTGTAGAAACAGTGTTGCCATATTCTCCAAACTGGTCTCAAACTCCTGGGCTCA TAATTTATTTTTTGTAGAAACAGTGTTGCCATGTTCTCCAAACTGGTCTCAAACTCCTGGGCTCA A G TAOK1 Ensembl:ENSG00000160551 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1317160829 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183084,RMVar_hsa_circ_326091,RMVar_hsa_circ_183082,RMVar_hsa_circ_90691,RMVar_hsa_circ_311255,RMVar_hsa_circ_183085,RMVar_hsa_circ_183083,RMVar_hsa_circ_369044,RMVar_hsa_circ_59753,RMVar_hsa_circ_183104,RMVar_hsa_circ_21785,RMVar_hsa_circ_183114,RMVar_hsa_circ_365610,RMVar_hsa_circ_376890,RMVar_hsa_circ_350043,RMVar_hsa_circ_278895,RMVar_hsa_circ_183113,RMVar_hsa_circ_275292,RMVar_hsa_circ_347311,RMVar_hsa_circ_338871,RMVar_hsa_circ_294129,RMVar_hsa_circ_183116,RMVar_hsa_circ_183117,RMVar_hsa_circ_183115,RMVar_hsa_circ_46343,RMVar_hsa_circ_339761,RMVar_hsa_circ_31703,RMVar_hsa_circ_47275,RMVar_hsa_circ_111637,RMVar_hsa_circ_357825,RMVar_hsa_circ_183130,RMVar_hsa_circ_266686,RMVar_hsa_circ_299530,RMVar_hsa_circ_183132,RMVar_hsa_circ_183133,RMVar_hsa_circ_306409,RMVar_hsa_circ_355627,RMVar_hsa_circ_366812 6807 RMVar_ID_6807 Human_SNP_ID_621420596 A-to-I Human chr17 + 29517981 29517980 29517981 GGGTGCAAGTGATTTTCGTGCCTCAGCCTCCCAAATAGCTAGGATTACAGGTGTGCACCACCACA GGGTGCAAGTGATTTTCGTGCCTCAGCCTCCC_AATAGCTAGGATTACAGGTGTGCACCACCACA CA C TAOK1 Ensembl:ENSG00000160551 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1274096964 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_183084,RMVar_hsa_circ_326091,RMVar_hsa_circ_183082,RMVar_hsa_circ_90691,RMVar_hsa_circ_311255,RMVar_hsa_circ_183085,RMVar_hsa_circ_183083,RMVar_hsa_circ_369044,RMVar_hsa_circ_59753,RMVar_hsa_circ_183104,RMVar_hsa_circ_21785,RMVar_hsa_circ_183114,RMVar_hsa_circ_365610,RMVar_hsa_circ_376890,RMVar_hsa_circ_350043,RMVar_hsa_circ_275292,RMVar_hsa_circ_347311,RMVar_hsa_circ_338871,RMVar_hsa_circ_183116,RMVar_hsa_circ_183115,RMVar_hsa_circ_46343,RMVar_hsa_circ_31703,RMVar_hsa_circ_47275,RMVar_hsa_circ_111637,RMVar_hsa_circ_183130,RMVar_hsa_circ_266686,RMVar_hsa_circ_299530,RMVar_hsa_circ_183132,RMVar_hsa_circ_183135,RMVar_hsa_circ_355627,RMVar_hsa_circ_366812,RMVar_hsa_circ_281268,RMVar_hsa_circ_357943,RMVar_hsa_circ_283749,RMVar_hsa_circ_183136 6808 RMVar_ID_6808 Human_SNP_ID_621420598 A-to-I Human chr17 + 29517989 29517989 29517989 GTGATTTTCGTGCCTCAGCCTCCCAAATAGCTAGGATTACAGGTGTGCACCACCACACCCAACTA GTGATTTTCGTGCCTCAGCCTCCCAAATAGCTGGGATTACAGGTGTGCACCACCACACCCAACTA A G TAOK1 Ensembl:ENSG00000160551 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs764155354 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183084,RMVar_hsa_circ_326091,RMVar_hsa_circ_183082,RMVar_hsa_circ_90691,RMVar_hsa_circ_311255,RMVar_hsa_circ_183085,RMVar_hsa_circ_183083,RMVar_hsa_circ_369044,RMVar_hsa_circ_59753,RMVar_hsa_circ_183104,RMVar_hsa_circ_21785,RMVar_hsa_circ_183114,RMVar_hsa_circ_365610,RMVar_hsa_circ_376890,RMVar_hsa_circ_350043,RMVar_hsa_circ_275292,RMVar_hsa_circ_347311,RMVar_hsa_circ_338871,RMVar_hsa_circ_183116,RMVar_hsa_circ_183115,RMVar_hsa_circ_46343,RMVar_hsa_circ_31703,RMVar_hsa_circ_47275,RMVar_hsa_circ_111637,RMVar_hsa_circ_183130,RMVar_hsa_circ_266686,RMVar_hsa_circ_299530,RMVar_hsa_circ_183132,RMVar_hsa_circ_183135,RMVar_hsa_circ_355627,RMVar_hsa_circ_366812,RMVar_hsa_circ_281268,RMVar_hsa_circ_357943,RMVar_hsa_circ_283749,RMVar_hsa_circ_183136 6809 RMVar_ID_6809 Human_SNP_ID_621420931 A-to-I Human chr17 + 29519329 29519329 29519329 GGTCAGGAGTTTGAGACCAGCCTGGCCAACATAGTGAAACCCCATCTCTACTTTTAGTAGAGATA GGTCAGGAGTTTGAGACCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTTTTAGTAGAGATA A G TAOK1 Ensembl:ENSG00000160551 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs776094757 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183084,RMVar_hsa_circ_326091,RMVar_hsa_circ_183082,RMVar_hsa_circ_90691,RMVar_hsa_circ_311255,RMVar_hsa_circ_183085,RMVar_hsa_circ_183083,RMVar_hsa_circ_369044,RMVar_hsa_circ_59753,RMVar_hsa_circ_183104,RMVar_hsa_circ_21785,RMVar_hsa_circ_183114,RMVar_hsa_circ_365610,RMVar_hsa_circ_376890,RMVar_hsa_circ_350043,RMVar_hsa_circ_275292,RMVar_hsa_circ_347311,RMVar_hsa_circ_338871,RMVar_hsa_circ_183116,RMVar_hsa_circ_183115,RMVar_hsa_circ_46343,RMVar_hsa_circ_31703,RMVar_hsa_circ_47275,RMVar_hsa_circ_111637,RMVar_hsa_circ_183130,RMVar_hsa_circ_266686,RMVar_hsa_circ_299530,RMVar_hsa_circ_183132,RMVar_hsa_circ_183135,RMVar_hsa_circ_355627,RMVar_hsa_circ_366812,RMVar_hsa_circ_281268,RMVar_hsa_circ_357943,RMVar_hsa_circ_283749,RMVar_hsa_circ_183136 6810 RMVar_ID_6810 Human_SNP_ID_621420952 A-to-I Human chr17 + 29519396 29519396 29519396 AACAAATGAGCCGGACGAGGTGGCGGGCGCCTATAATTCCAGCTACTCAGGAGGCTGAGGCATGA AACAAATGAGCCGGACGAGGTGGCGGGCGCCTGTAATTCCAGCTACTCAGGAGGCTGAGGCATGA A G TAOK1 Ensembl:ENSG00000160551 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs913817922 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183084,RMVar_hsa_circ_326091,RMVar_hsa_circ_183082,RMVar_hsa_circ_90691,RMVar_hsa_circ_311255,RMVar_hsa_circ_183085,RMVar_hsa_circ_183083,RMVar_hsa_circ_369044,RMVar_hsa_circ_59753,RMVar_hsa_circ_183104,RMVar_hsa_circ_21785,RMVar_hsa_circ_183114,RMVar_hsa_circ_365610,RMVar_hsa_circ_376890,RMVar_hsa_circ_350043,RMVar_hsa_circ_275292,RMVar_hsa_circ_347311,RMVar_hsa_circ_338871,RMVar_hsa_circ_183116,RMVar_hsa_circ_183115,RMVar_hsa_circ_46343,RMVar_hsa_circ_31703,RMVar_hsa_circ_47275,RMVar_hsa_circ_111637,RMVar_hsa_circ_183130,RMVar_hsa_circ_266686,RMVar_hsa_circ_299530,RMVar_hsa_circ_183132,RMVar_hsa_circ_183135,RMVar_hsa_circ_355627,RMVar_hsa_circ_366812,RMVar_hsa_circ_281268,RMVar_hsa_circ_357943,RMVar_hsa_circ_283749,RMVar_hsa_circ_183136 6811 RMVar_ID_6811 Human_SNP_ID_621421179 A-to-I Human chr17 + 29520450 29520450 29520450 TGTCTCTACAAATTTTTTTTTTTTGAGACTCTATTGCCCAGGCTGGAATGCAGTGGTGTGATCTC TGTCTCTACAAATTTTTTTTTTTTGAGACTCTGTTGCCCAGGCTGGAATGCAGTGGTGTGATCTC A G TAOK1 Ensembl:ENSG00000160551 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs944226368 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183084,RMVar_hsa_circ_326091,RMVar_hsa_circ_183082,RMVar_hsa_circ_90691,RMVar_hsa_circ_311255,RMVar_hsa_circ_183085,RMVar_hsa_circ_183083,RMVar_hsa_circ_369044,RMVar_hsa_circ_59753,RMVar_hsa_circ_183104,RMVar_hsa_circ_21785,RMVar_hsa_circ_183114,RMVar_hsa_circ_365610,RMVar_hsa_circ_376890,RMVar_hsa_circ_350043,RMVar_hsa_circ_275292,RMVar_hsa_circ_347311,RMVar_hsa_circ_338871,RMVar_hsa_circ_183116,RMVar_hsa_circ_183115,RMVar_hsa_circ_46343,RMVar_hsa_circ_31703,RMVar_hsa_circ_47275,RMVar_hsa_circ_111637,RMVar_hsa_circ_183130,RMVar_hsa_circ_266686,RMVar_hsa_circ_299530,RMVar_hsa_circ_183132,RMVar_hsa_circ_183135,RMVar_hsa_circ_355627,RMVar_hsa_circ_366812,RMVar_hsa_circ_281268,RMVar_hsa_circ_357943,RMVar_hsa_circ_283749,RMVar_hsa_circ_183136 6812 RMVar_ID_6812 Human_SNP_ID_621421286 A-to-I Human chr17 + 29520862 29520862 29520862 CCTGGCCAACATGGTGAAAACCCATCTATACTAAAGATACAAAAATTAGCCAGGCGTGGTGGCAC CCTGGCCAACATGGTGAAAACCCATCTATACTGAAGATACAAAAATTAGCCAGGCGTGGTGGCAC A G TAOK1 Ensembl:ENSG00000160551 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1365534587 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183084,RMVar_hsa_circ_326091,RMVar_hsa_circ_183082,RMVar_hsa_circ_90691,RMVar_hsa_circ_311255,RMVar_hsa_circ_183085,RMVar_hsa_circ_183083,RMVar_hsa_circ_369044,RMVar_hsa_circ_59753,RMVar_hsa_circ_183104,RMVar_hsa_circ_21785,RMVar_hsa_circ_183114,RMVar_hsa_circ_365610,RMVar_hsa_circ_376890,RMVar_hsa_circ_350043,RMVar_hsa_circ_275292,RMVar_hsa_circ_347311,RMVar_hsa_circ_338871,RMVar_hsa_circ_183116,RMVar_hsa_circ_183115,RMVar_hsa_circ_46343,RMVar_hsa_circ_31703,RMVar_hsa_circ_47275,RMVar_hsa_circ_111637,RMVar_hsa_circ_183130,RMVar_hsa_circ_266686,RMVar_hsa_circ_299530,RMVar_hsa_circ_183132,RMVar_hsa_circ_183135,RMVar_hsa_circ_355627,RMVar_hsa_circ_366812,RMVar_hsa_circ_281268,RMVar_hsa_circ_357943,RMVar_hsa_circ_283749,RMVar_hsa_circ_183136 6813 RMVar_ID_6813 Human_SNP_ID_621421776 A-to-I Human chr17 + 29522952 29522952 29522952 CAAAAATTAGTTGGGTGTGGCGGCACATGCCTATAGTCCCAGCTACTCGGGGGGCTGAAGCAGGA CAAAAATTAGTTGGGTGTGGCGGCACATGCCTGTAGTCCCAGCTACTCGGGGGGCTGAAGCAGGA A G TAOK1 Ensembl:ENSG00000160551 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs762092861 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25263261 RMVar_hsa_circ_183084,RMVar_hsa_circ_183082,RMVar_hsa_circ_90691,RMVar_hsa_circ_311255,RMVar_hsa_circ_183083,RMVar_hsa_circ_183114,RMVar_hsa_circ_365610,RMVar_hsa_circ_376890,RMVar_hsa_circ_347311,RMVar_hsa_circ_338871,RMVar_hsa_circ_183115,RMVar_hsa_circ_31703,RMVar_hsa_circ_47275,RMVar_hsa_circ_266686,RMVar_hsa_circ_355627,RMVar_hsa_circ_281268,RMVar_hsa_circ_357943,RMVar_hsa_circ_183136,RMVar_hsa_circ_266644,RMVar_hsa_circ_363054 6814 RMVar_ID_6814 Human_SNP_ID_621422356 A-to-I Human chr17 + 29525429 29525428 29525430 CACCATGCCCGACCTTGTTTTCTTTCTGAAACAGAGTTTCGCTCTTGTCGCCTAGGCTGGAGTGC CACCATGCCCGACCTTGTTTTCTTTCTGAAAC__AGTTTCGCTCTTGTCGCCTAGGCTGGAGTGC CAG C TAOK1 Ensembl:ENSG00000160551 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs575396225 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_183084,RMVar_hsa_circ_183082,RMVar_hsa_circ_90691,RMVar_hsa_circ_311255,RMVar_hsa_circ_183083,RMVar_hsa_circ_183114,RMVar_hsa_circ_365610,RMVar_hsa_circ_376890,RMVar_hsa_circ_347311,RMVar_hsa_circ_338871,RMVar_hsa_circ_183115,RMVar_hsa_circ_31703,RMVar_hsa_circ_47275,RMVar_hsa_circ_266686,RMVar_hsa_circ_355627,RMVar_hsa_circ_281268,RMVar_hsa_circ_357943,RMVar_hsa_circ_183136,RMVar_hsa_circ_266644,RMVar_hsa_circ_363054 6815 RMVar_ID_6815 Human_SNP_ID_621422557 A-to-I Human chr17 + 29526181 29526181 29526181 CTTGCTCTCCTAGCTACTTGGGAGGCTGAGGCAGGAGAATCACTTGAACCCGGAAGGCGGAGGAA CTTGCTCTCCTAGCTACTTGGGAGGCTGAGGCGGGAGAATCACTTGAACCCGGAAGGCGGAGGAA A G TAOK1 Ensembl:ENSG00000160551 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs529783102 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183084,RMVar_hsa_circ_183082,RMVar_hsa_circ_90691,RMVar_hsa_circ_311255,RMVar_hsa_circ_183083,RMVar_hsa_circ_183114,RMVar_hsa_circ_365610,RMVar_hsa_circ_376890,RMVar_hsa_circ_347311,RMVar_hsa_circ_338871,RMVar_hsa_circ_183115,RMVar_hsa_circ_31703,RMVar_hsa_circ_47275,RMVar_hsa_circ_266686,RMVar_hsa_circ_355627,RMVar_hsa_circ_281268,RMVar_hsa_circ_357943,RMVar_hsa_circ_183136,RMVar_hsa_circ_266644,RMVar_hsa_circ_363054 6816 RMVar_ID_6816 Human_SNP_ID_621423076 A-to-I Human chr17 + 29528300 29528300 29528300 TCAAACTCGACCTCAAATGATCTGGCCACCTCAGCCTCCCAAAGTGCTGGGATTGCAGGCGTGAG TCAAACTCGACCTCAAATGATCTGGCCACCTCGGCCTCCCAAAGTGCTGGGATTGCAGGCGTGAG A G TAOK1 Ensembl:ENSG00000160551 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1000163380 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183084,RMVar_hsa_circ_183082,RMVar_hsa_circ_90691,RMVar_hsa_circ_311255,RMVar_hsa_circ_183083,RMVar_hsa_circ_183114,RMVar_hsa_circ_365610,RMVar_hsa_circ_376890,RMVar_hsa_circ_347311,RMVar_hsa_circ_338871,RMVar_hsa_circ_183115,RMVar_hsa_circ_31703,RMVar_hsa_circ_47275,RMVar_hsa_circ_266686,RMVar_hsa_circ_355627,RMVar_hsa_circ_281268,RMVar_hsa_circ_357943,RMVar_hsa_circ_183136,RMVar_hsa_circ_266644,RMVar_hsa_circ_363054 6817 RMVar_ID_6817 Human_SNP_ID_621423295 A-to-I Human chr17 + 29529105 29529105 29529105 GTGATCCTTCTGCCTCAGCCTCCCTAGCAGCTAGGACTACAGGTGAACATCATTATGCCTGGCTA GTGATCCTTCTGCCTCAGCCTCCCTAGCAGCTGGGACTACAGGTGAACATCATTATGCCTGGCTA A G TAOK1 Ensembl:ENSG00000160551 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1045256169 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183084,RMVar_hsa_circ_183082,RMVar_hsa_circ_90691,RMVar_hsa_circ_311255,RMVar_hsa_circ_183083,RMVar_hsa_circ_183114,RMVar_hsa_circ_365610,RMVar_hsa_circ_376890,RMVar_hsa_circ_347311,RMVar_hsa_circ_338871,RMVar_hsa_circ_183115,RMVar_hsa_circ_31703,RMVar_hsa_circ_47275,RMVar_hsa_circ_266686,RMVar_hsa_circ_355627,RMVar_hsa_circ_281268,RMVar_hsa_circ_357943,RMVar_hsa_circ_183136,RMVar_hsa_circ_266644,RMVar_hsa_circ_363054 6818 RMVar_ID_6818 Human_SNP_ID_621423321 A-to-I Human chr17 + 29529238 29529238 29529238 CTATAAACAATCCTGCCTTGGCCTCCCAAAGTACTGGGATTACAGGCATGAGCCACAATAACTCT CTATAAACAATCCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACAATAACTCT A G TAOK1 Ensembl:ENSG00000160551 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1034740666 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183084,RMVar_hsa_circ_183082,RMVar_hsa_circ_90691,RMVar_hsa_circ_311255,RMVar_hsa_circ_183083,RMVar_hsa_circ_183114,RMVar_hsa_circ_365610,RMVar_hsa_circ_376890,RMVar_hsa_circ_347311,RMVar_hsa_circ_338871,RMVar_hsa_circ_183115,RMVar_hsa_circ_31703,RMVar_hsa_circ_47275,RMVar_hsa_circ_266686,RMVar_hsa_circ_355627,RMVar_hsa_circ_281268,RMVar_hsa_circ_357943,RMVar_hsa_circ_183136,RMVar_hsa_circ_266644,RMVar_hsa_circ_363054 6819 RMVar_ID_6819 Human_SNP_ID_621423348 A-to-I Human chr17 + 29529332 29529332 29529332 ATTTTCTAAGCCAGGTACAGTGGCTCATGCCTATAATTACTGTACTTTTAGGGGCTGAGGTGGGA ATTTTCTAAGCCAGGTACAGTGGCTCATGCCTGTAATTACTGTACTTTTAGGGGCTGAGGTGGGA A G TAOK1 Ensembl:ENSG00000160551 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1200186103 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183084,RMVar_hsa_circ_183082,RMVar_hsa_circ_90691,RMVar_hsa_circ_311255,RMVar_hsa_circ_183083,RMVar_hsa_circ_183114,RMVar_hsa_circ_365610,RMVar_hsa_circ_376890,RMVar_hsa_circ_347311,RMVar_hsa_circ_338871,RMVar_hsa_circ_183115,RMVar_hsa_circ_31703,RMVar_hsa_circ_47275,RMVar_hsa_circ_266686,RMVar_hsa_circ_355627,RMVar_hsa_circ_281268,RMVar_hsa_circ_357943,RMVar_hsa_circ_183136,RMVar_hsa_circ_266644,RMVar_hsa_circ_363054 6820 RMVar_ID_6820 Human_SNP_ID_621423444 A-to-I Human chr17 + 29529808 29529808 29529808 GAATCGGTTGAACTCAGGGAGGCGGCGGTTGCAGTGAGCCAAGATTGCGCCATTGGACTCCAGCC GAATCGGTTGAACTCAGGGAGGCGGCGGTTGCGGTGAGCCAAGATTGCGCCATTGGACTCCAGCC A G TAOK1 Ensembl:ENSG00000160551 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1194698805 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183084,RMVar_hsa_circ_183082,RMVar_hsa_circ_90691,RMVar_hsa_circ_311255,RMVar_hsa_circ_183083,RMVar_hsa_circ_183114,RMVar_hsa_circ_365610,RMVar_hsa_circ_376890,RMVar_hsa_circ_347311,RMVar_hsa_circ_338871,RMVar_hsa_circ_183115,RMVar_hsa_circ_31703,RMVar_hsa_circ_47275,RMVar_hsa_circ_266686,RMVar_hsa_circ_355627,RMVar_hsa_circ_281268,RMVar_hsa_circ_357943,RMVar_hsa_circ_183136,RMVar_hsa_circ_266644,RMVar_hsa_circ_363054 6821 RMVar_ID_6821 Human_SNP_ID_621423976 A-to-I Human chr17 + 29531586 29531586 29531586 AGAATTCGAGAGCAGCCTGCCCAACATGGCGAAACCTCGTCTCTACTAAAAATACAAAAATTAGC AGAATTCGAGAGCAGCCTGCCCAACATGGCGAGACCTCGTCTCTACTAAAAATACAAAAATTAGC A G TAOK1 Ensembl:ENSG00000160551 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1186526537 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183084,RMVar_hsa_circ_183082,RMVar_hsa_circ_90691,RMVar_hsa_circ_311255,RMVar_hsa_circ_183083,RMVar_hsa_circ_183114,RMVar_hsa_circ_376890,RMVar_hsa_circ_338871,RMVar_hsa_circ_31703,RMVar_hsa_circ_47275,RMVar_hsa_circ_266686,RMVar_hsa_circ_355627,RMVar_hsa_circ_281268,RMVar_hsa_circ_183136,RMVar_hsa_circ_363054,RMVar_hsa_circ_183137,RMVar_hsa_circ_311529 6822 RMVar_ID_6822 Human_SNP_ID_621423995 A-to-I Human chr17 + 29531640 29531640 29531640 CAAAAATTAGCCAGGCGTGGTGGTGGGCGCCCATAATCCCAGCTACTCTGGAGGCGGAGGCGGGA CAAAAATTAGCCAGGCGTGGTGGTGGGCGCCCTTAATCCCAGCTACTCTGGAGGCGGAGGCGGGA A T TAOK1 Ensembl:ENSG00000160551 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs911183698 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25263310 RMVar_hsa_circ_183084,RMVar_hsa_circ_183082,RMVar_hsa_circ_90691,RMVar_hsa_circ_311255,RMVar_hsa_circ_183083,RMVar_hsa_circ_183114,RMVar_hsa_circ_376890,RMVar_hsa_circ_338871,RMVar_hsa_circ_31703,RMVar_hsa_circ_47275,RMVar_hsa_circ_266686,RMVar_hsa_circ_355627,RMVar_hsa_circ_281268,RMVar_hsa_circ_183136,RMVar_hsa_circ_363054,RMVar_hsa_circ_183137,RMVar_hsa_circ_311529 6823 RMVar_ID_6823 Human_SNP_ID_621423996 A-to-I Human chr17 + 29531642 29531642 29531642 AAAATTAGCCAGGCGTGGTGGTGGGCGCCCATAATCCCAGCTACTCTGGAGGCGGAGGCGGGAGA AAAATTAGCCAGGCGTGGTGGTGGGCGCCCATGATCCCAGCTACTCTGGAGGCGGAGGCGGGAGA A G TAOK1 Ensembl:ENSG00000160551 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1416105554 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183084,RMVar_hsa_circ_183082,RMVar_hsa_circ_90691,RMVar_hsa_circ_311255,RMVar_hsa_circ_183083,RMVar_hsa_circ_183114,RMVar_hsa_circ_376890,RMVar_hsa_circ_338871,RMVar_hsa_circ_31703,RMVar_hsa_circ_47275,RMVar_hsa_circ_266686,RMVar_hsa_circ_355627,RMVar_hsa_circ_281268,RMVar_hsa_circ_183136,RMVar_hsa_circ_363054,RMVar_hsa_circ_183137,RMVar_hsa_circ_311529 6824 RMVar_ID_6824 Human_SNP_ID_621424021 A-to-I Human chr17 + 29531695 29531695 29531695 GGAGGCGGGAGAATCACCTGAACCCCGGGGGCAGAGGTTGCAGTGAGCCGAGATTGCGCCATTGC GGAGGCGGGAGAATCACCTGAACCCCGGGGGCGGAGGTTGCAGTGAGCCGAGATTGCGCCATTGC A G TAOK1 Ensembl:ENSG00000160551 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs920284416 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183084,RMVar_hsa_circ_183082,RMVar_hsa_circ_90691,RMVar_hsa_circ_311255,RMVar_hsa_circ_183083,RMVar_hsa_circ_183114,RMVar_hsa_circ_376890,RMVar_hsa_circ_338871,RMVar_hsa_circ_31703,RMVar_hsa_circ_47275,RMVar_hsa_circ_266686,RMVar_hsa_circ_355627,RMVar_hsa_circ_281268,RMVar_hsa_circ_183136,RMVar_hsa_circ_363054,RMVar_hsa_circ_183137,RMVar_hsa_circ_311529 6825 RMVar_ID_6825 Human_SNP_ID_621424153 A-to-I Human chr17 + 29532013 29532013 29532013 CTCCCGAATAGCTGAGACTACAGGCGCATGCCACCAAGCCCAGCTAATTTTTTGTATTTTTAGTG CTCCCGAATAGCTGAGACTACAGGCGCATGCCCCCAAGCCCAGCTAATTTTTTGTATTTTTAGTG A C TAOK1 Ensembl:ENSG00000160551 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs983079586 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183084,RMVar_hsa_circ_183082,RMVar_hsa_circ_90691,RMVar_hsa_circ_311255,RMVar_hsa_circ_183083,RMVar_hsa_circ_183114,RMVar_hsa_circ_376890,RMVar_hsa_circ_338871,RMVar_hsa_circ_31703,RMVar_hsa_circ_47275,RMVar_hsa_circ_266686,RMVar_hsa_circ_355627,RMVar_hsa_circ_281268,RMVar_hsa_circ_183136,RMVar_hsa_circ_363054,RMVar_hsa_circ_183137,RMVar_hsa_circ_311529 6826 RMVar_ID_6826 Human_SNP_ID_621426289 A-to-I Human chr17 + 29539141 29539141 29539141 AAAATTAGTTGGATATAGTGGTGTGCGCCTGTAGTACCAGCTCCTCTGGAGGCTGAGGTGTGGAG AAAATTAGTTGGATATAGTGGTGTGCGCCTGTGGTACCAGCTCCTCTGGAGGCTGAGGTGTGGAG A G TAOK1 Ensembl:ENSG00000160551 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1340974181 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183082,RMVar_hsa_circ_90691,RMVar_hsa_circ_183083,RMVar_hsa_circ_82344,RMVar_hsa_circ_183138 6827 RMVar_ID_6827 Human_SNP_ID_621426587 A-to-I Human chr17 + 29540401 29540401 29540401 TGTTTGTTTGTTTTGAGACTAAGTCCCATTCTATTGCCCAGGCTGGAGTGCAGTAGCCCCATCTT TGTTTGTTTGTTTTGAGACTAAGTCCCATTCTGTTGCCCAGGCTGGAGTGCAGTAGCCCCATCTT A G TAOK1 Ensembl:ENSG00000160551 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs151210950 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183082,RMVar_hsa_circ_90691,RMVar_hsa_circ_183083,RMVar_hsa_circ_82344,RMVar_hsa_circ_183138 6828 RMVar_ID_6828 Human_SNP_ID_621426790 A-to-I Human chr17 + 29541262 29541262 29541262 CTCCCAAGAAGCAGGGATTACAGACGTGTGCCACCGCGCCTGGCTAATTTTTGTATTTTTAGTAG CTCCCAAGAAGCAGGGATTACAGACGTGTGCCCCCGCGCCTGGCTAATTTTTGTATTTTTAGTAG A C TAOK1 Ensembl:ENSG00000160551 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1003172272 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183082,RMVar_hsa_circ_90691,RMVar_hsa_circ_183083,RMVar_hsa_circ_82344,RMVar_hsa_circ_183138 6829 RMVar_ID_6829 Human_SNP_ID_621426890 A-to-I Human chr17 + 29541629 29541629 29541629 GAAACCCCATCTCTACTAAAAATACAAAAATTAGCTGGATGTGGTAGCACATGCCTGTAATCCCA GAAACCCCATCTCTACTAAAAATACAAAAATTGGCTGGATGTGGTAGCACATGCCTGTAATCCCA A G TAOK1 Ensembl:ENSG00000160551 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1361982650 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183082,RMVar_hsa_circ_90691,RMVar_hsa_circ_183083,RMVar_hsa_circ_82344,RMVar_hsa_circ_183138 6830 RMVar_ID_6830 Human_SNP_ID_621426894 A-to-I Human chr17 + 29541655 29541655 29541655 AAAATTAGCTGGATGTGGTAGCACATGCCTGTAATCCCAGCTACATGGGAGGCTGAGGCTAGAGA AAAATTAGCTGGATGTGGTAGCACATGCCTGTGATCCCAGCTACATGGGAGGCTGAGGCTAGAGA A G TAOK1 Ensembl:ENSG00000160551 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs755247405 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183082,RMVar_hsa_circ_90691,RMVar_hsa_circ_183083,RMVar_hsa_circ_82344,RMVar_hsa_circ_183138 6831 RMVar_ID_6831 Human_SNP_ID_621426906 A-to-I Human chr17 + 29541730 29541730 29541730 CCCAGGATGCGGAGGTTGCAGTGAGCTGAGATAGTGACATTCCACTCCAGCCCAGGCGACAGTGC CCCAGGATGCGGAGGTTGCAGTGAGCTGAGATCGTGACATTCCACTCCAGCCCAGGCGACAGTGC A C TAOK1 Ensembl:ENSG00000160551 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1305008519 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25263345 RMVar_hsa_circ_183082,RMVar_hsa_circ_90691,RMVar_hsa_circ_183083,RMVar_hsa_circ_82344,RMVar_hsa_circ_183138 6832 RMVar_ID_6832 Human_SNP_ID_621431508 A-to-I Human chr17 - 29560715 29560715 29560715 GGGAGGCGGAGCTTGCAGTGAGCTGAGATCGCACCACTGCACTCCAGCCTGGGCGACAGAGTAAG GGGAGGCGGAGCTTGCAGTGAGCTGAGATCGCGCCACTGCACTCCAGCCTGGGCGACAGAGTAAG T C ABHD15 Ensembl:ENSG00000168792 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs930119625 Functional Loss SNV dbSNP153 33..33 33 - - - 6833 RMVar_ID_6833 Human_SNP_ID_621431509 A-to-I Human chr17 - 29560715 29560715 29560715 GGGAGGCGGAGCTTGCAGTGAGCTGAGATCGCACCACTGCACTCCAGCCTGGGCGACAGAGTAAG GGGAGGCGGAGCTTGCAGTGAGCTGAGATCGCCCCACTGCACTCCAGCCTGGGCGACAGAGTAAG T G ABHD15 Ensembl:ENSG00000168792 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs930119625 Functional Loss SNV dbSNP153 33..33 33 - - - 6834 RMVar_ID_6834 Human_SNP_ID_621434477 A-to-I Human chr17 + 29569949 29569949 29569949 CTTATTATTATTATTATTTGAAATGGAATCTCACTCTGTTGCCCAGGCTGGAGTGCAGTGGCACT CTTATTATTATTATTATTTGAAATGGAATCTCGCTCTGTTGCCCAGGCTGGAGTGCAGTGGCACT A G TP53I13,AC104564.3,ABHD15-AS1 Ensembl:ENSG00000167543,Ensembl:ENSG00000264290,Ensembl:ENSG00000264031 Protein coding,lincRNA,lincRNA intron,exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1371593609 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183142,RMVar_hsa_circ_106650 6835 RMVar_ID_6835 Human_SNP_ID_621444797 A-to-I Human chr17 + 29605987 29605987 29605987 CAGGCTGGAGTGCAGTGGCATGATCTCGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGCGGTT CAGGCTGGAGTGCAGTGGCATGATCTCGGCTCGCTGCAACCTCCGCCTCCCGGGTTCAAGCGGTT A G ABHD15-AS1,ANKRD13B Ensembl:ENSG00000264031,Ensembl:ENSG00000198720 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1044021818 Functional Loss SNV dbSNP153 33..33 33 - - - 6836 RMVar_ID_6836 Human_SNP_ID_621447330 A-to-I Human chr17 + 29614358 29614358 29614358 AGTGGGGAGCATATTGGGCTGGGGTAAGCACTAGACCCAAGTAGACTGGACACAAAGGGCTCGCC AGTGGGGAGCATATTGGGCTGGGGTAAGCACTGGACCCAAGTAGACTGGACACAAAGGGCTCGCC A G ABHD15-AS1,ANKRD13B Ensembl:ENSG00000264031,Ensembl:ENSG00000198720 lincRNA,Protein coding intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs777025921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1131823,Human_RBP_ID_5466298,Human_RBP_ID_5580691,Human_RBP_ID_8192752,Human_RBP_ID_12948229,Human_RBP_ID_18290515,Human_RBP_ID_26458883 Human_miRNA_ID_474142,Human_miRNA_ID_1563613,Human_miRNA_ID_2843880,Human_miRNA_ID_3114688 RMVar_hsa_circ_95205,RMVar_hsa_circ_183159 6837 RMVar_ID_6837 Human_SNP_ID_621453709 A-to-I Human chr17 - 29637700 29637700 29637700 TCAGCTCACTGCATCCTCACCCTCCTGGGTTCAAGCAATCCTCCCACCTCAGCCCCCTGAGTAGC TCAGCTCACTGCATCCTCACCCTCCTGGGTTCTAGCAATCCTCCCACCTCAGCCCCCTGAGTAGC T A SSH2 Ensembl:ENSG00000141298 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1010862788 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23718981 RMVar_hsa_circ_32468,RMVar_hsa_circ_116148,RMVar_hsa_circ_90513,RMVar_hsa_circ_101763,RMVar_hsa_circ_326053,RMVar_hsa_circ_183164,RMVar_hsa_circ_183165,RMVar_hsa_circ_377613,RMVar_hsa_circ_183163,RMVar_hsa_circ_353074,RMVar_hsa_circ_318516,RMVar_hsa_circ_299000,RMVar_hsa_circ_183169,RMVar_hsa_circ_183170 6838 RMVar_ID_6838 Human_SNP_ID_621455083 A-to-I Human chr17 - 29643689 29643689 29643689 AGGAGTTCGAGACCAGCCTGGCCAACATGGCTAAACCCCGTCTCTACTAAAAATACAAAAATTAG AGGAGTTCGAGACCAGCCTGGCCAACATGGCTGAACCCCGTCTCTACTAAAAATACAAAAATTAG T C SSH2 Ensembl:ENSG00000141298 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs755573484 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32468,RMVar_hsa_circ_116148,RMVar_hsa_circ_90513,RMVar_hsa_circ_101763,RMVar_hsa_circ_326053,RMVar_hsa_circ_183164,RMVar_hsa_circ_183165,RMVar_hsa_circ_377613,RMVar_hsa_circ_183163,RMVar_hsa_circ_353074,RMVar_hsa_circ_318516,RMVar_hsa_circ_299000,RMVar_hsa_circ_183169,RMVar_hsa_circ_183170 6839 RMVar_ID_6839 Human_SNP_ID_621461795 A-to-I Human chr17 - 29673510 29673510 29673510 GCTGGAGTGCAGTGGCACCATCTCAGCTAACTACAGCCTCCGTCTCCCAGGTTCAAGCGATTCTC GCTGGAGTGCAGTGGCACCATCTCAGCTAACTGCAGCCTCCGTCTCCCAGGTTCAAGCGATTCTC T C SSH2 Ensembl:ENSG00000141298 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031419093 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25263536 RMVar_hsa_circ_116148,RMVar_hsa_circ_90513,RMVar_hsa_circ_101763,RMVar_hsa_circ_183164,RMVar_hsa_circ_183165,RMVar_hsa_circ_183163,RMVar_hsa_circ_353074,RMVar_hsa_circ_24996,RMVar_hsa_circ_183174,RMVar_hsa_circ_183172,RMVar_hsa_circ_89282,RMVar_hsa_circ_75798,RMVar_hsa_circ_336019,RMVar_hsa_circ_183171,RMVar_hsa_circ_352588,RMVar_hsa_circ_334863,RMVar_hsa_circ_277386,RMVar_hsa_circ_183175,RMVar_hsa_circ_183173,RMVar_hsa_circ_376730,RMVar_hsa_circ_9226,RMVar_hsa_circ_81308,RMVar_hsa_circ_183180,RMVar_hsa_circ_303841,RMVar_hsa_circ_183186,RMVar_hsa_circ_183189,RMVar_hsa_circ_278071,RMVar_hsa_circ_322525,RMVar_hsa_circ_315410,RMVar_hsa_circ_298644,RMVar_hsa_circ_183190,RMVar_hsa_circ_183188,RMVar_hsa_circ_378507,RMVar_hsa_circ_378612,RMVar_hsa_circ_309421,RMVar_hsa_circ_357633,RMVar_hsa_circ_29932,RMVar_hsa_circ_183191 6840 RMVar_ID_6840 Human_SNP_ID_621462840 A-to-I Human chr17 - 29678210 29678210 29678210 GCTCGCCTGTAATCCCAGCTACTGGGGAGGCTAAGGCAGGGGAATTGCTTGAACCTGGGAGGCAG GCTCGCCTGTAATCCCAGCTACTGGGGAGGCTGAGGCAGGGGAATTGCTTGAACCTGGGAGGCAG T C SSH2 Ensembl:ENSG00000141298 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1309914568 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90513,RMVar_hsa_circ_101763,RMVar_hsa_circ_183164,RMVar_hsa_circ_183163,RMVar_hsa_circ_353074,RMVar_hsa_circ_24996,RMVar_hsa_circ_183172,RMVar_hsa_circ_75798,RMVar_hsa_circ_336019,RMVar_hsa_circ_334863,RMVar_hsa_circ_183173,RMVar_hsa_circ_376730,RMVar_hsa_circ_183180,RMVar_hsa_circ_303841,RMVar_hsa_circ_183189,RMVar_hsa_circ_278071,RMVar_hsa_circ_322525,RMVar_hsa_circ_315410,RMVar_hsa_circ_378612,RMVar_hsa_circ_357633,RMVar_hsa_circ_29932,RMVar_hsa_circ_75661,RMVar_hsa_circ_76984,RMVar_hsa_circ_125151,RMVar_hsa_circ_183191,RMVar_hsa_circ_285861,RMVar_hsa_circ_183194,RMVar_hsa_circ_183195,RMVar_hsa_circ_319165,RMVar_hsa_circ_296408,RMVar_hsa_circ_125995,RMVar_hsa_circ_183197,RMVar_hsa_circ_183199,RMVar_hsa_circ_183201,RMVar_hsa_circ_183200,RMVar_hsa_circ_183198,RMVar_hsa_circ_183196 6841 RMVar_ID_6841 Human_SNP_ID_621469725 A-to-I Human chr17 - 29707623 29707623 29707623 TGTTCGCGAGGCTGAGGCACGAGAATCGTTTGAGCCCAGGAGGCAGAGGTTGCAGTGAGCCAAGA TGTTCGCGAGGCTGAGGCACGAGAATCGTTTGCGCCCAGGAGGCAGAGGTTGCAGTGAGCCAAGA T G SSH2 Ensembl:ENSG00000141298 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs541602643 Functional Loss SNV dbSNP153 33..33 33 - - - 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_183198,RMVar_hsa_circ_183208,RMVar_hsa_circ_183196,RMVar_hsa_circ_376304,RMVar_hsa_circ_26469 6842 RMVar_ID_6842 Human_SNP_ID_621479747 A-to-I Human chr17 - 29749864 29749864 29749864 AAATTAATCGGGCGTGGTGGCGGGCACCTGTAATCTCAGCTACTCAGGAGACTGAGGCAGGAGAA AAATTAATCGGGCGTGGTGGCGGGCACCTGTAGTCTCAGCTACTCAGGAGACTGAGGCAGGAGAA T C SSH2 Ensembl:ENSG00000141298 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1303645006 Functional Loss SNV dbSNP153 33..33 33 - - - 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 6843 RMVar_ID_6843 Human_SNP_ID_621480599 A-to-I Human chr17 - 29753406 29753406 29753406 AGCAGATAAGCCGGGCGCAGTGGCTCACACCTATAATCCCAGCACTTTGGGAGGCTGAGGTTGGG AGCAGATAAGCCGGGCGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGTTGGG T C SSH2 Ensembl:ENSG00000141298 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs545871002 Functional Loss SNV dbSNP153 33..33 33 - - - 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 6844 RMVar_ID_6844 Human_SNP_ID_621481120 A-to-I Human chr17 - 29755800 29755800 29755800 AAAATTAGCCGGGTGCGGTGGCGGGTGCCTGTAGTCCCAGCCACTCAGCAGGCTGAGGCAGGAGA AAAATTAGCCGGGTGCGGTGGCGGGTGCCTGTGGTCCCAGCCACTCAGCAGGCTGAGGCAGGAGA T C SSH2 Ensembl:ENSG00000141298 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941448127 Functional Loss SNV dbSNP153 33..33 33 - - - 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 6845 RMVar_ID_6845 Human_SNP_ID_621481121 A-to-I Human chr17 - 29755800 29755800 29755800 AAAATTAGCCGGGTGCGGTGGCGGGTGCCTGTAGTCCCAGCCACTCAGCAGGCTGAGGCAGGAGA AAAATTAGCCGGGTGCGGTGGCGGGTGCCTGTCGTCCCAGCCACTCAGCAGGCTGAGGCAGGAGA T G SSH2 Ensembl:ENSG00000141298 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941448127 Functional Loss SNV dbSNP153 33..33 33 - - - 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 6846 RMVar_ID_6846 Human_SNP_ID_621481455 A-to-I Human chr17 - 29756884 29756884 29756884 TTGAGAGGCTGAGGCAGATGGATCACGAGGTCAGGAGTTCGAGACCAGCCTGGCCAGCATGGTGA TTGAGAGGCTGAGGCAGATGGATCACGAGGTCCGGAGTTCGAGACCAGCCTGGCCAGCATGGTGA T G SSH2 Ensembl:ENSG00000141298 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs955891859 Functional Loss SNV dbSNP153 33..33 33 - - - 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 6847 RMVar_ID_6847 Human_SNP_ID_621493099 A-to-I Human chr17 - 29809684 29809684 29809684 GGGCACGGTGGTGTGTGCCTGTAGTCTCAGTTACTCAGGAGGCTGAGGTGGGGGAATCTCTTGAA GGGCACGGTGGTGTGTGCCTGTAGTCTCAGTTGCTCAGGAGGCTGAGGTGGGGGAATCTCTTGAA T C SSH2 Ensembl:ENSG00000141298 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1050092833 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4443,RMVar_hsa_circ_101763,RMVar_hsa_circ_183163,RMVar_hsa_circ_125995,RMVar_hsa_circ_183196,RMVar_hsa_circ_72845 6848 RMVar_ID_6848 Human_SNP_ID_621497352 A-to-I Human chr17 - 29829672 29829672 29829672 TTCCCCAGCAATCAGTACAATGTCTAGCACATAGGAGGTACTCTGTACATATTGGTTAAAAGAAG TTCCCCAGCAATCAGTACAATGTCTAGCACATTGGAGGTACTCTGTACATATTGGTTAAAAGAAG T A SSH2 Ensembl:ENSG00000141298 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1331450828 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4443,RMVar_hsa_circ_101763,RMVar_hsa_circ_183163,RMVar_hsa_circ_125995,RMVar_hsa_circ_183196,RMVar_hsa_circ_72845 6849 RMVar_ID_6849 Human_SNP_ID_621509608 A-to-I Human chr17 - 29888169 29888169 29888169 CAGTGGCATGATCATGGCTCACTGCAGCCTCAACCTTCTGGGCTCAAGTAATTCTCCTGCCTCAG CAGTGGCATGATCATGGCTCACTGCAGCCTCAGCCTTCTGGGCTCAAGTAATTCTCCTGCCTCAG T C SSH2 Ensembl:ENSG00000141298 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982198369 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101763,RMVar_hsa_circ_183163,RMVar_hsa_circ_125995,RMVar_hsa_circ_183196 6850 RMVar_ID_6850 Human_SNP_ID_621512624 A-to-I Human chr17 - 29902038 29902038 29902038 TTATGCCTGTAATCCCAACACTTTGGAAGGCCAAGGTAGGAGGATCCCTTGAGGCCAGGAGTTCA TTATGCCTGTAATCCCAACACTTTGGAAGGCCGAGGTAGGAGGATCCCTTGAGGCCAGGAGTTCA T C SSH2 Ensembl:ENSG00000141298 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1485670633 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101763,RMVar_hsa_circ_183163,RMVar_hsa_circ_125995,RMVar_hsa_circ_183196 6851 RMVar_ID_6851 Human_SNP_ID_399859694 A-to-I Human chr9 - 61857069 61857069 61857069 GACCTGGTAGCCCTGACGCAACTTCGGCTGGCACAAACCCACAGAGAGTGGGAAAGAAACACACA GACCTGGTAGCCCTGACGCAACTTCGGCTGGCTCAAACCCACAGAGAGTGGGAAAGAAACACACA T A - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1218754531 Functional Loss SNV dbSNP153 33..33 33 - - - 6852 RMVar_ID_6852 Human_SNP_ID_399917839 A-to-I Human chr9 + 62421749 62421749 62421749 CTCTGACCTTAGCCTCCTGAGTAGCTGGAACTACAGGTGCATGCCACCATGCCTGGCTAATTAAT CTCTGACCTTAGCCTCCTGAGTAGCTGGAACTGCAGGTGCATGCCACCATGCCTGGCTAATTAAT A G FGF7P6 Ensembl:ENSG00000227449 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1281343998 Functional Loss SNV dbSNP153 33..33 33 - - - 6853 RMVar_ID_6853 Human_SNP_ID_400065815 A-to-I Human chr9 - 63320870 63320870 63320870 AAAATAGTTGGGCATGGTGGCATGCACCTATAATCTCAACTACTCGGGAGGCTAAGGCAGGAGAA AAAATAGTTGGGCATGGTGGCATGCACCTATAGTCTCAACTACTCGGGAGGCTAAGGCAGGAGAA T C BMS1P10,AQP7P1 Ensembl:ENSG00000237238,Ensembl:ENSG00000186466 Pseudogene,Pseudogene intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1250904225 Functional Loss SNV dbSNP153 33..33 33 - - - 6854 RMVar_ID_6854 Human_SNP_ID_400065830 A-to-I Human chr9 - 63320907 63320907 63320907 CAACATCGTGAAACCCTGTCTCTACTAAAAATACAAAAAAATAGTTGGGCATGGTGGCATGCACC CAACATCGTGAAACCCTGTCTCTACTAAAAATGCAAAAAAATAGTTGGGCATGGTGGCATGCACC T C BMS1P10,AQP7P1 Ensembl:ENSG00000237238,Ensembl:ENSG00000186466 Pseudogene,Pseudogene intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1480327014 Functional Loss SNV dbSNP153 33..33 33 - - - 6855 RMVar_ID_6855 Human_SNP_ID_400206251 A-to-I Human chr9 - 63834282 63834282 63834282 AGGAGGCTGAGACAGGAGGATTGTTTGAGCCCAGGAGTTCAAGGCTGCAGTGAGCTCTGATCACC AGGAGGCTGAGACAGGAGGATTGTTTGAGCCCTGGAGTTCAAGGCTGCAGTGAGCTCTGATCACC T A FRG1JP Ensembl:ENSG00000215548 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1416358334 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64073 6856 RMVar_ID_6856 Human_SNP_ID_400552170 A-to-I Human chr9 - 65314472 65314472 65314472 TGGTTTGAGACAGAATCTCACTGTGTCCCCCAAGTTGGAGTGCGGTGGTGCGATCTCGGCTCACT TGGTTTGAGACAGAATCTCACTGTGTCCCCCAGGTTGGAGTGCGGTGGTGCGATCTCGGCTCACT T C CBWD4P Ensembl:ENSG00000204778 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1338977646 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16755805 6857 RMVar_ID_6857 Human_SNP_ID_400552171 A-to-I Human chr9 - 65314472 65314472 65314472 TGGTTTGAGACAGAATCTCACTGTGTCCCCCAAGTTGGAGTGCGGTGGTGCGATCTCGGCTCACT TGGTTTGAGACAGAATCTCACTGTGTCCCCCACGTTGGAGTGCGGTGGTGCGATCTCGGCTCACT T G CBWD4P Ensembl:ENSG00000204778 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1338977646 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16755805 6858 RMVar_ID_6858 Human_SNP_ID_400552174 A-to-I Human chr9 - 65314485 65314482 65314486 CAGAATCTCACTCTGGTTTGAGACAGAATCTCACTGTGTCCCCCAAGTTGGAGTGCGGTGGTGCG CAGAATCTCACTCTGGTTTGAGACAGAATCT____GTGTCCCCCAAGTTGGAGTGCGGTGGTGCG CAGTG C CBWD4P Ensembl:ENSG00000204778 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1451660506 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_16755805 6859 RMVar_ID_6859 Human_SNP_ID_400625128 A-to-I Human chr9 - 65668944 65668944 65668944 TGTCCTCCTGAGGGGATGAACACTGTGTGTTCACCTGGCAGAAGGAGACAGAAATAAGCTTTCAC TGTCCTCCTGAGGGGATGAACACTGTGTGTTCGCCTGGCAGAAGGAGACAGAAATAAGCTTTCAC T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1421787696 Functional Loss SNV dbSNP153 33..33 33 - - - 6860 RMVar_ID_6860 Human_SNP_ID_400633372 A-to-I Human chr9 + 65700310 65700310 65700310 CATTAATAAAACAGACTTGGTTCCAGAAGAAGATGTAAAGAAATTAAGAACGACAATTAGGTACA CATTAATAAAACAGACTTGGTTCCAGAAGAAGGTGTAAAGAAATTAAGAACGACAATTAGGTACA A G CBWD5 Ensembl:ENSG00000147996 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1461274264 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1047856,Human_Splice_Rec_1047857,Human_Splice_Rec_1047886,Human_Splice_Rec_1047887,Human_Splice_Rec_1047916,Human_Splice_Rec_1047917,Human_Splice_Rec_1047946,Human_Splice_Rec_1047947,Human_Splice_Rec_1047974,Human_Splice_Rec_1047975,Human_Splice_Rec_1048000,Human_Splice_Rec_1048001,Human_Splice_Rec_1048056,Human_Splice_Rec_1048057,Human_Splice_Rec_1048082,Human_Splice_Rec_1048083,Human_Splice_Rec_1048112,Human_Splice_Rec_1048113,Human_Splice_Rec_1048136,Human_Splice_Rec_1048137,Human_Splice_Rec_1048192,Human_Splice_Rec_1048206,Human_Splice_Rec_1048207,Human_Splice_Rec_1048220,Human_Splice_Rec_1048221,Human_Splice_Rec_1048252,Human_Splice_Rec_1048253,Human_Splice_Rec_1048262,Human_Splice_Rec_1048266,Human_Splice_Rec_1048267,Human_Splice_Rec_1048269 RMVar_hsa_circ_2723,RMVar_hsa_circ_52493,RMVar_hsa_circ_352217,RMVar_hsa_circ_363215,RMVar_hsa_circ_360272,RMVar_hsa_circ_43260,RMVar_hsa_circ_10781,RMVar_hsa_circ_18472,RMVar_hsa_circ_42681,RMVar_hsa_circ_36654 6861 RMVar_ID_6861 Human_SNP_ID_400634270 A-to-I Human chr9 - 65704650 65704650 65704650 CCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCACCCAGCCCAAATCTCCAGTT CCTTGGCCTCCCAAAGTGCTGGGATTACAGGCTTGAGCCACCGCACCCAGCCCAAATCTCCAGTT T A - - Other Unknown GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1470379982 Functional Loss SNV dbSNP153 33..33 33 - - - 6862 RMVar_ID_6862 Human_SNP_ID_400634271 A-to-I Human chr9 - 65704650 65704650 65704650 CCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCACCCAGCCCAAATCTCCAGTT CCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCACCCAGCCCAAATCTCCAGTT T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1470379982 Functional Loss SNV dbSNP153 33..33 33 - - - 6863 RMVar_ID_6863 Human_SNP_ID_401012652 A-to-I Human chr9 - 68235001 68235001 68235001 TGTCCTCCTGAGGGGATGAACACTGTGTGTTCACCTGGCAGAAGGAGACAGAAATAAGCTTTCAC TGTCCTCCTGAGGGGATGAACACTGTGTGTTCGCCTGGCAGAAGGAGACAGAAATAAGCTTTCAC T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs797035381 Functional Loss SNV dbSNP153 33..33 33 - - - 6864 RMVar_ID_6864 Human_SNP_ID_401142028 A-to-I Human chr9 + 68784205 68784205 68784205 TTCATAACGTCCATCATTATTCTGTAGACTGTAAGGGCTTACTTAGCTCGTGTAAGAATTATCCT TTCATAACGTCCATCATTATTCTGTAGACTGTGAGGGCTTACTTAGCTCGTGTAAGAATTATCCT A G FAM122A,PIP5K1B Ensembl:ENSG00000187866,Ensembl:ENSG00000107242 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1311604048 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18909594 6865 RMVar_ID_6865 Human_SNP_ID_401209188 A-to-I Human chr9 + 69075902 69075902 69075902 AATTTGTGTATTTTTTGTAGAGATGGGGTTTCACCATGTTGCCCAGGCTGGTCTCTAACACTTAG AATTTGTGTATTTTTTGTAGAGATGGGGTTTCGCCATGTTGCCCAGGCTGGTCTCTAACACTTAG A G AL358113.1,FXN Ensembl:ENSG00000285130,Ensembl:ENSG00000165060 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1282527949 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_257025 6866 RMVar_ID_6866 Human_SNP_ID_401209199 A-to-I Human chr9 + 69075939 69075939 69075939 GTTGCCCAGGCTGGTCTCTAACACTTAGGCTCAAGTGATCCACCTGCCTCGTCCTCCCAAGATGC GTTGCCCAGGCTGGTCTCTAACACTTAGGCTCTAGTGATCCACCTGCCTCGTCCTCCCAAGATGC A T AL358113.1,FXN Ensembl:ENSG00000285130,Ensembl:ENSG00000165060 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs974615124 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_257025 6867 RMVar_ID_6867 Human_SNP_ID_401209447 A-to-I Human chr9 + 69076938 69076937 69076939 TAGAGTAAGAAATGCCTTTTCTTTTTTGAGACAGAGTCTTGCTCTGTCACCCAGGCTGGAGTGCA TAGAGTAAGAAATGCCTTTTCTTTTTTGAGAC__AGTCTTGCTCTGTCACCCAGGCTGGAGTGCA CAG C AL358113.1,FXN Ensembl:ENSG00000285130,Ensembl:ENSG00000165060 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1478786806 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_257025 6868 RMVar_ID_6868 Human_SNP_ID_401209505 A-to-I Human chr9 + 69077173 69077173 69077173 TGACCTAGTAATCCACCTGCCTCCGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCAC TGACCTAGTAATCCACCTGCCTCCGCCTCCCAGAGTGCTGGGATTACAGGCGTGAGCCACTGCAC A G AL358113.1,FXN Ensembl:ENSG00000285130,Ensembl:ENSG00000165060 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1337972751 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_257025 6869 RMVar_ID_6869 Human_SNP_ID_401209856 A-to-I Human chr9 + 69078649 69078649 69078649 TACCCCCTCACACTCAACACTTTGACTCCAGCAATCCCAAATCCCCAGATCCCTAAGTGTGCTGT TACCCCCTCACACTCAACACTTTGACTCCAGCGATCCCAAATCCCCAGATCCCTAAGTGTGCTGT A G AL358113.1,FXN Ensembl:ENSG00000285130,Ensembl:ENSG00000165060 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569435256 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_257025 6870 RMVar_ID_6870 Human_SNP_ID_401215670 A-to-I Human chr9 + 69102060 69102060 69102060 GCACGTCTGTAGTCCCAGCTACTGGGAAGACTAAAGTGAGAGAACTGCTTGAGCCCAGAGGTCGA GCACGTCTGTAGTCCCAGCTACTGGGAAGACTGAAGTGAGAGAACTGCTTGAGCCCAGAGGTCGA A G AL358113.1 Ensembl:ENSG00000285130 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs999536012 Functional Loss SNV dbSNP153 33..33 33 - - - 6871 RMVar_ID_6871 Human_SNP_ID_401246336 A-to-I Human chr9 + 69223437 69223437 69223437 TCACACCATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTGTAGGCGCCCGCCACCACACCCG TCACACCATTCTCCTGCCTCAGCCTCCCAAGTTGCTGGGACTGTAGGCGCCCGCCACCACACCCG A T TJP2,AL358113.1 Ensembl:ENSG00000119139,Ensembl:ENSG00000285130 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1182258511 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60440,RMVar_hsa_circ_377966,RMVar_hsa_circ_54414,RMVar_hsa_circ_68473,RMVar_hsa_circ_23691,RMVar_hsa_circ_355517,RMVar_hsa_circ_121491,RMVar_hsa_circ_62793,RMVar_hsa_circ_54019,RMVar_hsa_circ_257026 6872 RMVar_ID_6872 Human_SNP_ID_401504428 A-to-I Human chr9 + 70304431 70304431 70304431 TCAATAGGTCGGGCACAGTGACTCATGCTTATAATCCTAGCACTTTGGGAGGCCAAGGCAAGCCG TCAATAGGTCGGGCACAGTGACTCATGCTTATGATCCTAGCACTTTGGGAGGCCAAGGCAAGCCG A G SMC5 Ensembl:ENSG00000198887 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs920069454 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84117,RMVar_hsa_circ_257064,RMVar_hsa_circ_125615,RMVar_hsa_circ_104729,RMVar_hsa_circ_257067,RMVar_hsa_circ_112896,RMVar_hsa_circ_265842,RMVar_hsa_circ_93479,RMVar_hsa_circ_108886,RMVar_hsa_circ_257070,RMVar_hsa_circ_257071,RMVar_hsa_circ_371839,RMVar_hsa_circ_257074,RMVar_hsa_circ_99480,RMVar_hsa_circ_257075,RMVar_hsa_circ_257073,RMVar_hsa_circ_70218,RMVar_hsa_circ_257079,RMVar_hsa_circ_94318,RMVar_hsa_circ_257080,RMVar_hsa_circ_56349,RMVar_hsa_circ_103828,RMVar_hsa_circ_353024,RMVar_hsa_circ_52623,RMVar_hsa_circ_257082 6873 RMVar_ID_6873 Human_SNP_ID_401508675 A-to-I Human chr9 + 70321620 70321620 70321620 CTGGGGCTGGTCTCGAACACCAGACCTCAATCAGTCCTCCCGCCTCAGCCTCCCAAAGTGCTAGG CTGGGGCTGGTCTCGAACACCAGACCTCAATCCGTCCTCCCGCCTCAGCCTCCCAAAGTGCTAGG A C SMC5 Ensembl:ENSG00000198887 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1035346231 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26227462 RMVar_hsa_circ_84117,RMVar_hsa_circ_257064,RMVar_hsa_circ_125615,RMVar_hsa_circ_104729,RMVar_hsa_circ_257067,RMVar_hsa_circ_112896,RMVar_hsa_circ_265842,RMVar_hsa_circ_108886,RMVar_hsa_circ_257070,RMVar_hsa_circ_257071,RMVar_hsa_circ_371839,RMVar_hsa_circ_257074,RMVar_hsa_circ_99480,RMVar_hsa_circ_257075,RMVar_hsa_circ_257073,RMVar_hsa_circ_70218,RMVar_hsa_circ_94318,RMVar_hsa_circ_257080,RMVar_hsa_circ_103828,RMVar_hsa_circ_52623,RMVar_hsa_circ_70028,RMVar_hsa_circ_97992,RMVar_hsa_circ_257082,RMVar_hsa_circ_257084,RMVar_hsa_circ_308924,RMVar_hsa_circ_126926,RMVar_hsa_circ_257083,RMVar_hsa_circ_293643,RMVar_hsa_circ_42235,RMVar_hsa_circ_45302,RMVar_hsa_circ_257086,RMVar_hsa_circ_257085,RMVar_hsa_circ_257087,RMVar_hsa_circ_118200 6874 RMVar_ID_6874 Human_SNP_ID_401512520 A-to-I Human chr9 + 70337724 70337724 70337724 ATGATCCACCCGCCTCGGCCTCCCAAAGTGCTAGGATTACAGGTGTGAGCCACTACACCTGGCCA ATGATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACTACACCTGGCCA A G SMC5 Ensembl:ENSG00000198887 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1405774319 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_257064,RMVar_hsa_circ_125615,RMVar_hsa_circ_104729,RMVar_hsa_circ_257067,RMVar_hsa_circ_112896,RMVar_hsa_circ_108886,RMVar_hsa_circ_257071,RMVar_hsa_circ_257074,RMVar_hsa_circ_99480,RMVar_hsa_circ_257073,RMVar_hsa_circ_94318,RMVar_hsa_circ_257080,RMVar_hsa_circ_103828,RMVar_hsa_circ_257088,RMVar_hsa_circ_97992,RMVar_hsa_circ_257082,RMVar_hsa_circ_257084,RMVar_hsa_circ_126926,RMVar_hsa_circ_42235,RMVar_hsa_circ_45302,RMVar_hsa_circ_257086,RMVar_hsa_circ_126596,RMVar_hsa_circ_257087,RMVar_hsa_circ_118200,RMVar_hsa_circ_315823,RMVar_hsa_circ_359013,RMVar_hsa_circ_287275,RMVar_hsa_circ_257089,RMVar_hsa_circ_257090,RMVar_hsa_circ_92249 6875 RMVar_ID_6875 Human_SNP_ID_401512655 A-to-I Human chr9 + 70338291 70338291 70338291 CCTCGGCCTCCCAAAGTACTGGGATTACAGGCATGTGCCACCATGCCCAGCCATTTGCATAATTT CCTCGGCCTCCCAAAGTACTGGGATTACAGGCGTGTGCCACCATGCCCAGCCATTTGCATAATTT A G SMC5 Ensembl:ENSG00000198887 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1188237128 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_257064,RMVar_hsa_circ_125615,RMVar_hsa_circ_104729,RMVar_hsa_circ_257067,RMVar_hsa_circ_112896,RMVar_hsa_circ_108886,RMVar_hsa_circ_257071,RMVar_hsa_circ_257074,RMVar_hsa_circ_99480,RMVar_hsa_circ_257073,RMVar_hsa_circ_94318,RMVar_hsa_circ_257080,RMVar_hsa_circ_103828,RMVar_hsa_circ_257088,RMVar_hsa_circ_97992,RMVar_hsa_circ_257082,RMVar_hsa_circ_257084,RMVar_hsa_circ_126926,RMVar_hsa_circ_42235,RMVar_hsa_circ_45302,RMVar_hsa_circ_257086,RMVar_hsa_circ_126596,RMVar_hsa_circ_257087,RMVar_hsa_circ_118200,RMVar_hsa_circ_315823,RMVar_hsa_circ_359013,RMVar_hsa_circ_287275,RMVar_hsa_circ_257089,RMVar_hsa_circ_257090,RMVar_hsa_circ_92249 6876 RMVar_ID_6876 Human_SNP_ID_401814677 A-to-I Human chr9 + 71589582 71589582 71589582 CATCTTGGCTCCTGTGGAGGCCTGCTGGGAACAGGACTTCTAAAAGGAACTATATCTGGAAGGCT CATCTTGGCTCCTGTGGAGGCCTGCTGGGAACCGGACTTCTAAAAGGAACTATATCTGGAAGGCT A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1486908634 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5030958,Human_RBP_ID_17716712,Human_RBP_ID_26566803 6877 RMVar_ID_6877 Human_SNP_ID_401814683 A-to-I Human chr9 + 71589603 71589603 71589603 CTGCTGGGAACAGGACTTCTAAAAGGAACTATATCTGGAAGGCTGTGGTCCAATGCCATTTTTGC CTGCTGGGAACAGGACTTCTAAAAGGAACTATGTCTGGAAGGCTGTGGTCCAATGCCATTTTTGC A G RPL35AP21 Ensembl:ENSG00000229814 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559447636 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26564104 Human_miRNA_ID_1827413 6878 RMVar_ID_6878 Human_SNP_ID_401838409 A-to-I Human chr9 - 71687964 71687964 71687964 TAGTCTCACCTACTGAGGAGGCTAGGACAGGAAGATCCCTTGAGCCCAAGAGTTTGAGGCTGCAG TAGTCTCACCTACTGAGGAGGCTAGGACAGGAGGATCCCTTGAGCCCAAGAGTTTGAGGCTGCAG T C CEMIP2 Ensembl:ENSG00000135048 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1307331247 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17579291 RMVar_hsa_circ_88121,RMVar_hsa_circ_65755,RMVar_hsa_circ_109070,RMVar_hsa_circ_257112,RMVar_hsa_circ_257113 6879 RMVar_ID_6879 Human_SNP_ID_401849475 A-to-I Human chr9 - 71728924 71728924 71728924 TGGGAGGCTGGGGTGGGAGGATACTTGAGCCCAGGAGGTGGAGGCTGCTGTGAGCCAAGATTGCG TGGGAGGCTGGGGTGGGAGGATACTTGAGCCCCGGAGGTGGAGGCTGCTGTGAGCCAAGATTGCG T G CEMIP2 Ensembl:ENSG00000135048 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1279345136 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16694519,Human_RBP_ID_17579292 RMVar_hsa_circ_69455,RMVar_hsa_circ_109070,RMVar_hsa_circ_265277,RMVar_hsa_circ_257113,RMVar_hsa_circ_364243,RMVar_hsa_circ_47808,RMVar_hsa_circ_43415,RMVar_hsa_circ_58750,RMVar_hsa_circ_13412,RMVar_hsa_circ_75409,RMVar_hsa_circ_359905,RMVar_hsa_circ_75019,RMVar_hsa_circ_257123,RMVar_hsa_circ_356255,RMVar_hsa_circ_257124,RMVar_hsa_circ_257125 6880 RMVar_ID_6880 Human_SNP_ID_401892927 A-to-I Human chr9 - 71907575 71907575 71907575 CCCAGGAGGCAGAGGTTGTGGTGAGCCAAGATAGCACCATTGCACTCCAGCGTGGGCAGCAAGAG CCCAGGAGGCAGAGGTTGTGGTGAGCCAAGATGGCACCATTGCACTCCAGCGTGGGCAGCAAGAG T C ABHD17B Ensembl:ENSG00000107362 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1465751484 Functional Loss SNV dbSNP153 33..33 33 - - - 6881 RMVar_ID_6881 Human_SNP_ID_401894424 A-to-I Human chr9 + 71912723 71912723 71912723 CCTGGCCAACATGGCGAAACTCCCAATCTGCTAAAAATACAAAAATTAGCCGACGTGGTGACGGG CCTGGCCAACATGGCGAAACTCCCAATCTGCTGAAAATACAAAAATTAGCCGACGTGGTGACGGG A G C9orf85 Ensembl:ENSG00000155621 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs916615538 Functional Loss SNV dbSNP153 33..33 33 - - - 6882 RMVar_ID_6882 Human_SNP_ID_401901141 A-to-I Human chr9 + 71943707 71943707 71943707 TAGGATTACAGGCATGCGCCAGCACCCCGGCTAATTTTGTACTTTTAGTAGAGACGGGGTTTCTC TAGGATTACAGGCATGCGCCAGCACCCCGGCTGATTTTGTACTTTTAGTAGAGACGGGGTTTCTC A G C9orf85 Ensembl:ENSG00000155621 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1158441164 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_257139,RMVar_hsa_circ_280566,RMVar_hsa_circ_337769 6883 RMVar_ID_6883 Human_SNP_ID_401903437 A-to-I Human chr9 + 71953865 71953865 71953865 TCACACCTGTAATCCCAGCACTTTGAGAAGCTAAGGCAGGAGGATCACTTGATTCTAGGAGTTTG TCACACCTGTAATCCCAGCACTTTGAGAAGCTGAGGCAGGAGGATCACTTGATTCTAGGAGTTTG A G C9orf85 Ensembl:ENSG00000155621 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1433433800 Functional Loss SNV dbSNP153 33..33 33 - - - 6884 RMVar_ID_6884 Human_SNP_ID_401905049 A-to-I Human chr9 + 71961195 71961195 71961195 CGGTCTCCCAGAGTGCTGGGATTTACAGGTGTAAGCCACCACGCCTGGCCTCCAGCATTTCTTAT CGGTCTCCCAGAGTGCTGGGATTTACAGGTGTGAGCCACCACGCCTGGCCTCCAGCATTTCTTAT A G C9orf85 Ensembl:ENSG00000155621 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334316429 Functional Loss SNV dbSNP153 33..33 33 - - - 6885 RMVar_ID_6885 Human_SNP_ID_401908242 A-to-I Human chr9 + 71973108 71973103 71973108 CGGAGATTGAAGTGAGCTGAGTTCGTGCCATTACACTCCAGCCTGGGTGACAGAGTGAGACTCTG CGGAGATTGAAGTGAGCTGAGTTCGTGC_____CACTCCAGCCTGGGTGACAGAGTGAGACTCTG CCATTA C C9orf85 Ensembl:ENSG00000155621 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1190186291 Functional Loss DEL dbSNP153 29..33 33 - - - Human_miRNA_ID_97292,Human_miRNA_ID_1771909 6886 RMVar_ID_6886 Human_SNP_ID_401908244 A-to-I Human chr9 + 71973108 71973108 71973108 CGGAGATTGAAGTGAGCTGAGTTCGTGCCATTACACTCCAGCCTGGGTGACAGAGTGAGACTCTG CGGAGATTGAAGTGAGCTGAGTTCGTGCCATTTCACTCCAGCCTGGGTGACAGAGTGAGACTCTG A T C9orf85 Ensembl:ENSG00000155621 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1159202961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_97292,Human_miRNA_ID_1771909 6887 RMVar_ID_6887 Human_SNP_ID_401908611 A-to-I Human chr9 + 71974401 71974401 71974401 TAGTAGCGGGGACTGCAGGCCTGCACCACCACACCTGGGTAATTTTTGTATTTTTAGTAGAGACG TAGTAGCGGGGACTGCAGGCCTGCACCACCACGCCTGGGTAATTTTTGTATTTTTAGTAGAGACG A G C9orf85 Ensembl:ENSG00000155621 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs763526503 Functional Loss SNV dbSNP153 33..33 33 - - - 6888 RMVar_ID_6888 Human_SNP_ID_401908908 A-to-I Human chr9 + 71975651 71975651 71975651 GGTCGGGAGTTCGAGACCAGCCTGACCAACACAGAGAAACCCCATCTCTACTAAAAACACAAAAT GGTCGGGAGTTCGAGACCAGCCTGACCAACACGGAGAAACCCCATCTCTACTAAAAACACAAAAT A G C9orf85 Ensembl:ENSG00000155621 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1407985075 Functional Loss SNV dbSNP153 33..33 33 - - - 6889 RMVar_ID_6889 Human_SNP_ID_401975405 A-to-I Human chr9 + 72257049 72257049 72257049 GTGATCCTCCCACCTCAGCATTCTAAAGTGCTAGGATTACAGACATGAGCTACTGCACCCAGCCA GTGATCCTCCCACCTCAGCATTCTAAAGTGCTGGGATTACAGACATGAGCTACTGCACCCAGCCA A G GDA Ensembl:ENSG00000119125 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215019457 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1052150 6890 RMVar_ID_6890 Human_SNP_ID_402191184 A-to-I Human chr9 + 73154497 73154497 73154497 TTGTTATGTCGCCCAGGATGGAGTGTAGTGGTACAATCTCGGCTCACTGCAGCCTCCGCCTCTTC TTGTTATGTCGCCCAGGATGGAGTGTAGTGGTGCAATCTCGGCTCACTGCAGCCTCCGCCTCTTC A G ANXA1 Ensembl:ENSG00000135046 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1412162237 Functional Loss SNV dbSNP153 33..33 33 - - - 6891 RMVar_ID_6891 Human_SNP_ID_402359254 A-to-I Human chr9 - 73846234 73846234 73846234 CTTATAAATTCATAGATTACCTGTTTTCCCCCAGAGTTTTAGATTTGGCTCACAAAGTGTACTTT CTTATAAATTCATAGATTACCTGTTTTCCCCCCGAGTTTTAGATTTGGCTCACAAAGTGTACTTT T G lnc-ALDH1A1-10 RNACentral:URS0000D5D5CA lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs571264200 Functional Loss SNV dbSNP153 33..33 33 - - - 6892 RMVar_ID_6892 Human_SNP_ID_564645765 A-to-I Human chr14 + 90031598 90031598 90031598 AGAACTGCTTGAACCCGGGTGGCAGAGGCTGCAGTGAGCCGAGATCACACCACTGCACTCCAGAC AGAACTGCTTGAACCCGGGTGGCAGAGGCTGCGGTGAGCCGAGATCACACCACTGCACTCCAGAC A G TDP1 Ensembl:ENSG00000042088 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1203653505 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_282519,RMVar_hsa_circ_168475,RMVar_hsa_circ_330776,RMVar_hsa_circ_168477,RMVar_hsa_circ_18201,RMVar_hsa_circ_290119,RMVar_hsa_circ_168478,RMVar_hsa_circ_266495,RMVar_hsa_circ_326682,RMVar_hsa_circ_168485,RMVar_hsa_circ_366605 6893 RMVar_ID_6893 Human_SNP_ID_564701199 A-to-I Human chr14 + 90265998 90265998 90265998 AAGCTCTATTCTGAGCATGGTGGCTCATGCCTATAATCCTAGCACTGTGAGAGGTCAAGGCGGAT AAGCTCTATTCTGAGCATGGTGGCTCATGCCTGTAATCCTAGCACTGTGAGAGGTCAAGGCGGAT A G PSMC1 Ensembl:ENSG00000100764 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs369703411 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110444,RMVar_hsa_circ_168487,RMVar_hsa_circ_80921,RMVar_hsa_circ_168488,RMVar_hsa_circ_88224,RMVar_hsa_circ_371330,RMVar_hsa_circ_125226,RMVar_hsa_circ_168489,RMVar_hsa_circ_168490,RMVar_hsa_circ_168491 6894 RMVar_ID_6894 Human_SNP_ID_564701530 A-to-I Human chr14 + 90267265 90267233 90267265 GATTCTCCTGCCTTAGCCTCTCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTAGG G________________________________ATTCTCCTGCCTCAGCCTCCCGAGTAGCTAGG GATTCTCCTGCCTTAGCCTCTCGGGTTCAAGCA G PSMC1 Ensembl:ENSG00000100764 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1473446806 Functional Loss DEL dbSNP153 2..33 33 - - - RMVar_hsa_circ_110444,RMVar_hsa_circ_168487,RMVar_hsa_circ_80921,RMVar_hsa_circ_168488,RMVar_hsa_circ_88224,RMVar_hsa_circ_371330,RMVar_hsa_circ_125226,RMVar_hsa_circ_168489,RMVar_hsa_circ_168490,RMVar_hsa_circ_168491 6895 RMVar_ID_6895 Human_SNP_ID_564701537 A-to-I Human chr14 + 90267265 90267265 90267265 GATTCTCCTGCCTTAGCCTCTCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTAGG GATTCTCCTGCCTTAGCCTCTCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTAGG A G PSMC1 Ensembl:ENSG00000100764 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903010756 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110444,RMVar_hsa_circ_168487,RMVar_hsa_circ_80921,RMVar_hsa_circ_168488,RMVar_hsa_circ_88224,RMVar_hsa_circ_371330,RMVar_hsa_circ_125226,RMVar_hsa_circ_168489,RMVar_hsa_circ_168490,RMVar_hsa_circ_168491 6896 RMVar_ID_6896 Human_SNP_ID_564702988 A-to-I Human chr14 - 90273215 90273215 90273215 GTAACTTGTTATAGTATTAACAGAAAACTAATACACACTCCTCATTCAGTGTGGGCCCTACAACC GTAACTTGTTATAGTATTAACAGAAAACTAATTCACACTCCTCATTCAGTGTGGGCCCTACAACC T A NRDE2 Ensembl:ENSG00000119720 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10143776 Functional Loss SNV dbSNP153 33..33 33 - - - 6897 RMVar_ID_6897 Human_SNP_ID_564702989 A-to-I Human chr14 - 90273215 90273215 90273215 GTAACTTGTTATAGTATTAACAGAAAACTAATACACACTCCTCATTCAGTGTGGGCCCTACAACC GTAACTTGTTATAGTATTAACAGAAAACTAATGCACACTCCTCATTCAGTGTGGGCCCTACAACC T C NRDE2 Ensembl:ENSG00000119720 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10143776 Functional Loss SNV dbSNP153 33..33 33 - - - 6898 RMVar_ID_6898 Human_SNP_ID_564705407 A-to-I Human chr14 - 90281271 90281270 90281271 CAGGTGCGCACCACTGTGCTGGGCTAATTTTTATATTTTTGTAGAGACAGCGTTTTGCCATGTTG CAGGTGCGCACCACTGTGCTGGGCTAATTTTT_TATTTTTGTAGAGACAGCGTTTTGCCATGTTG AT A NRDE2 Ensembl:ENSG00000119720 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1306470624 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_12440247 RMVar_hsa_circ_3399,RMVar_hsa_circ_9884,RMVar_hsa_circ_168492 6899 RMVar_ID_6899 Human_SNP_ID_564777496 A-to-I Human chr14 - 90564651 90564651 90564651 TCCCAACTCTGCCTCTCAAAAGTGTTGAAATTACAGGCCTGAACCACTGTGCCCAGCCCAGCAGT TCCCAACTCTGCCTCTCAAAAGTGTTGAAATTGCAGGCCTGAACCACTGTGCCCAGCCCAGCAGT T C TTC7B Ensembl:ENSG00000165914 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs970960622 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_168504,RMVar_hsa_circ_90909 6900 RMVar_ID_6900 Human_SNP_ID_564798884 A-to-I Human chr14 - 90655034 90655034 90655034 AGAGAAAACGTCAGAGTTCAAGGCCAAAGGCTACTTAGCTCTGGGGCTCACGTACAGTCTGCAGG AGAGAAAACGTCAGAGTTCAAGGCCAAAGGCTGCTTAGCTCTGGGGCTCACGTACAGTCTGCAGG T C TTC7B Ensembl:ENSG00000165914 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1468688741 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3945056 Human_Splice_Rec_1544804,Human_Splice_Rec_1544805,Human_Splice_Rec_1544830,Human_Splice_Rec_1544831,Human_Splice_Rec_1544906,Human_Splice_Rec_1544907,Human_Splice_Rec_1544914,Human_Splice_Rec_1544915,Human_Splice_Rec_1544926,Human_Splice_Rec_1544927 RMVar_hsa_circ_168504,RMVar_hsa_circ_90909,RMVar_hsa_circ_311365,RMVar_hsa_circ_26407,RMVar_hsa_circ_33094,RMVar_hsa_circ_337775,RMVar_hsa_circ_349245,RMVar_hsa_circ_300924,RMVar_hsa_circ_168512,RMVar_hsa_circ_11202,RMVar_hsa_circ_42783,RMVar_hsa_circ_10446,RMVar_hsa_circ_168521,RMVar_hsa_circ_168515,RMVar_hsa_circ_168516,RMVar_hsa_circ_270058,RMVar_hsa_circ_288826,RMVar_hsa_circ_308932,RMVar_hsa_circ_298526,RMVar_hsa_circ_287616,RMVar_hsa_circ_126842,RMVar_hsa_circ_168519,RMVar_hsa_circ_168520,RMVar_hsa_circ_168518,RMVar_hsa_circ_29468,RMVar_hsa_circ_103414,RMVar_hsa_circ_168523,RMVar_hsa_circ_168524 6901 RMVar_ID_6901 Human_SNP_ID_564822411 A-to-I Human chr14 - 90757324 90757324 90757324 TACTCCTACCTTGTCCTCCCAAAGTGCTGGGAATACAGATGTGAGCCACCGCGCCAGGACTGCTT TACTCCTACCTTGTCCTCCCAAAGTGCTGGGATTACAGATGTGAGCCACCGCGCCAGGACTGCTT T A TTC7B Ensembl:ENSG00000165914 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs922024839 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_168504,RMVar_hsa_circ_90909,RMVar_hsa_circ_311365,RMVar_hsa_circ_33094,RMVar_hsa_circ_337775,RMVar_hsa_circ_300924,RMVar_hsa_circ_168512,RMVar_hsa_circ_168516,RMVar_hsa_circ_298526,RMVar_hsa_circ_29468,RMVar_hsa_circ_291492,RMVar_hsa_circ_45408,RMVar_hsa_circ_168528,RMVar_hsa_circ_325648,RMVar_hsa_circ_336445,RMVar_hsa_circ_312985,RMVar_hsa_circ_168533,RMVar_hsa_circ_314456,RMVar_hsa_circ_272885,RMVar_hsa_circ_168537,RMVar_hsa_circ_13814,RMVar_hsa_circ_168536,RMVar_hsa_circ_291186,RMVar_hsa_circ_168538 6902 RMVar_ID_6902 Human_SNP_ID_564822412 A-to-I Human chr14 - 90757324 90757324 90757324 TACTCCTACCTTGTCCTCCCAAAGTGCTGGGAATACAGATGTGAGCCACCGCGCCAGGACTGCTT TACTCCTACCTTGTCCTCCCAAAGTGCTGGGAGTACAGATGTGAGCCACCGCGCCAGGACTGCTT T C TTC7B Ensembl:ENSG00000165914 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs922024839 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_168504,RMVar_hsa_circ_90909,RMVar_hsa_circ_311365,RMVar_hsa_circ_33094,RMVar_hsa_circ_337775,RMVar_hsa_circ_300924,RMVar_hsa_circ_168512,RMVar_hsa_circ_168516,RMVar_hsa_circ_298526,RMVar_hsa_circ_29468,RMVar_hsa_circ_291492,RMVar_hsa_circ_45408,RMVar_hsa_circ_168528,RMVar_hsa_circ_325648,RMVar_hsa_circ_336445,RMVar_hsa_circ_312985,RMVar_hsa_circ_168533,RMVar_hsa_circ_314456,RMVar_hsa_circ_272885,RMVar_hsa_circ_168537,RMVar_hsa_circ_13814,RMVar_hsa_circ_168536,RMVar_hsa_circ_291186,RMVar_hsa_circ_168538 6903 RMVar_ID_6903 Human_SNP_ID_564910132 A-to-I Human chr14 + 91115684 91115684 91115684 CATCCGGCCTGGCCTCCCAAAGTGCTGGGATTATAGGCGTGAGCCACCACACCTAGCCAGGAAGC CATCCGGCCTGGCCTCCCAAAGTGCTGGGATTGTAGGCGTGAGCCACCACACCTAGCCAGGAAGC A G DGLUCY Ensembl:ENSG00000133943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs755883654 Functional Loss SNV dbSNP153 33..33 33 - - - 6904 RMVar_ID_6904 Human_SNP_ID_564911749 A-to-I Human chr14 + 91122168 91122167 91122168 AGTAATTTTATTAAGGAGCTTTTTATTTTTTTATTTTTTTTTTTGAGACAGGGTCCCACCCTGTT AGTAATTTTATTAAGGAGCTTTTTATTTTTTT_TTTTTTTTTTTGAGACAGGGTCCCACCCTGTT TA T DGLUCY Ensembl:ENSG00000133943 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1455362455 Functional Loss DEL dbSNP153 33..33 33 - - - 6905 RMVar_ID_6905 Human_SNP_ID_564911750 A-to-I Human chr14 + 91122168 91122168 91122168 AGTAATTTTATTAAGGAGCTTTTTATTTTTTTATTTTTTTTTTTGAGACAGGGTCCCACCCTGTT AGTAATTTTATTAAGGAGCTTTTTATTTTTTTTTTTTTTTTTTTGAGACAGGGTCCCACCCTGTT A T DGLUCY Ensembl:ENSG00000133943 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1212578485 Functional Loss SNV dbSNP153 33..33 33 - - - 6906 RMVar_ID_6906 Human_SNP_ID_564912243 A-to-I Human chr14 + 91124111 91124111 91124111 CATCATGCCCGGCTAATTTTTGTATTTTTAGTAGTGACGGGGTTTCACCATGTTGGCTGGGATGG CATCATGCCCGGCTAATTTTTGTATTTTTAGTCGTGACGGGGTTTCACCATGTTGGCTGGGATGG A C DGLUCY Ensembl:ENSG00000133943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1007864405 Functional Loss SNV dbSNP153 33..33 33 - - - 6907 RMVar_ID_6907 Human_SNP_ID_564912356 A-to-I Human chr14 + 91124644 91124644 91124644 ACTCTGATTCTGTGGTTAATCAGAAACAAATCAGCCTGTTTCATAGAAGCCTTTGTTGTTTGTTC ACTCTGATTCTGTGGTTAATCAGAAACAAATCGGCCTGTTTCATAGAAGCCTTTGTTGTTTGTTC A G DGLUCY Ensembl:ENSG00000133943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4900070 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_292,GWAS_ID_293,GWAS_ID_294,GWAS_ID_295,GWAS_ID_296,GWAS_ID_297,GWAS_ID_298,GWAS_ID_299,GWAS_ID_300,GWAS_ID_301,GWAS_ID_302,GWAS_ID_303,GWAS_ID_304,GWAS_ID_305,GWAS_ID_306,GWAS_ID_307,GWAS_ID_308,GWAS_ID_309 6908 RMVar_ID_6908 Human_SNP_ID_564912357 A-to-I Human chr14 + 91124644 91124644 91124644 ACTCTGATTCTGTGGTTAATCAGAAACAAATCAGCCTGTTTCATAGAAGCCTTTGTTGTTTGTTC ACTCTGATTCTGTGGTTAATCAGAAACAAATCTGCCTGTTTCATAGAAGCCTTTGTTGTTTGTTC A T DGLUCY Ensembl:ENSG00000133943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4900070 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_292,GWAS_ID_293,GWAS_ID_294,GWAS_ID_295,GWAS_ID_296,GWAS_ID_297,GWAS_ID_298,GWAS_ID_299,GWAS_ID_300,GWAS_ID_301,GWAS_ID_302,GWAS_ID_303,GWAS_ID_304,GWAS_ID_305,GWAS_ID_306,GWAS_ID_307,GWAS_ID_308,GWAS_ID_309 6909 RMVar_ID_6909 Human_SNP_ID_564913256 A-to-I Human chr14 + 91128215 91128215 91128215 AAAGATCCAGGCCGGTACGGTGGCTCACACCTATAATCCCAGCACTTTGGGAGGCTGAGGCAGGT AAAGATCCAGGCCGGTACGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGT A G DGLUCY Ensembl:ENSG00000133943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1276670889 Functional Loss SNV dbSNP153 33..33 33 - - - 6910 RMVar_ID_6910 Human_SNP_ID_564914196 A-to-I Human chr14 + 91131973 91131973 91131973 GTGCCACCACACCCAGCTAATTTTGTATTTTTAGTAGAGACAGGGTTTCTCCATGTTCGTCAGGC GTGCCACCACACCCAGCTAATTTTGTATTTTTGGTAGAGACAGGGTTTCTCCATGTTCGTCAGGC A G DGLUCY Ensembl:ENSG00000133943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs964411491 Functional Loss SNV dbSNP153 33..33 33 - - - 6911 RMVar_ID_6911 Human_SNP_ID_564914276 A-to-I Human chr14 + 91132378 91132378 91132378 CTTGAGCCTAGGAGTTCAAGACCAGGCAGGGCAACATAGTGAGATCCCATCTCTACCAAAAAATA CTTGAGCCTAGGAGTTCAAGACCAGGCAGGGCCACATAGTGAGATCCCATCTCTACCAAAAAATA A C DGLUCY Ensembl:ENSG00000133943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs534547913 Functional Loss SNV dbSNP153 33..33 33 - - - 6912 RMVar_ID_6912 Human_SNP_ID_564914926 A-to-I Human chr14 + 91135004 91135004 91135004 TGGAGTGCATTGGTGTGATCTCTGCTCATTGCAACCTCCCCCTCCCAGGCTCAAGCAATCCTCCC TGGAGTGCATTGGTGTGATCTCTGCTCATTGCGACCTCCCCCTCCCAGGCTCAAGCAATCCTCCC A G DGLUCY Ensembl:ENSG00000133943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs545536395 Functional Loss SNV dbSNP153 33..33 33 - - - 6913 RMVar_ID_6913 Human_SNP_ID_564916773 A-to-I Human chr14 + 91142120 91142120 91142120 CATCTGCCTCTGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCATCGTGCCCGGCCAGAGAGG CATCTGCCTCTGCCTCCCAAAGTGCTGGGATTGCAGGCGTGAGCCATCGTGCCCGGCCAGAGAGG A G DGLUCY Ensembl:ENSG00000133943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1361029391 Functional Loss SNV dbSNP153 33..33 33 - - - 6914 RMVar_ID_6914 Human_SNP_ID_564918256 A-to-I Human chr14 + 91147964 91147956 91147965 GGGAGGCTGAGGCAGGTGGATCACTTAAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATAGTGA GGGAGGCTGAGGCAGGTGGATCACT_________GAGTTCAAGACCAGCCTGGCCAACATAGTGA TTAAGGTCAG T DGLUCY Ensembl:ENSG00000133943 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1566966180 Functional Loss DEL dbSNP153 26..34 33 - - - RMVar_hsa_circ_39467,RMVar_hsa_circ_91919,RMVar_hsa_circ_303039,RMVar_hsa_circ_168567,RMVar_hsa_circ_168568,RMVar_hsa_circ_32656,RMVar_hsa_circ_366483 6915 RMVar_ID_6915 Human_SNP_ID_564918267 A-to-I Human chr14 + 91148003 91148003 91148003 CAAGACCAGCCTGGCCAACATAGTGAAACCCCATTTCTACTAAAAATACAAAAATTAGCCAGGTG CAAGACCAGCCTGGCCAACATAGTGAAACCCCGTTTCTACTAAAAATACAAAAATTAGCCAGGTG A G DGLUCY Ensembl:ENSG00000133943 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs539927010 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39467,RMVar_hsa_circ_91919,RMVar_hsa_circ_303039,RMVar_hsa_circ_168567,RMVar_hsa_circ_168568,RMVar_hsa_circ_32656,RMVar_hsa_circ_366483 6916 RMVar_ID_6916 Human_SNP_ID_564918280 A-to-I Human chr14 + 91148053 91148053 91148053 AAAATTAGCCAGGTGCAGTGGCACGCACCTGTAATCCCAGCTACTTGGGAGGGTGAGGCAGGAGA AAAATTAGCCAGGTGCAGTGGCACGCACCTGTGATCCCAGCTACTTGGGAGGGTGAGGCAGGAGA A G DGLUCY Ensembl:ENSG00000133943 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs925432933 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39467,RMVar_hsa_circ_91919,RMVar_hsa_circ_303039,RMVar_hsa_circ_168567,RMVar_hsa_circ_168568,RMVar_hsa_circ_32656,RMVar_hsa_circ_366483 6917 RMVar_ID_6917 Human_SNP_ID_564918382 A-to-I Human chr14 + 91148445 91148445 91148445 TCAGGCTGGTCTCGAACTCCTGAGCTCAAGCGATCCACCCACCTTGGCCTCTCAAAGTGCTGGGA TCAGGCTGGTCTCGAACTCCTGAGCTCAAGCGTTCCACCCACCTTGGCCTCTCAAAGTGCTGGGA A T DGLUCY Ensembl:ENSG00000133943 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs957406384 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39467,RMVar_hsa_circ_91919,RMVar_hsa_circ_303039,RMVar_hsa_circ_168567,RMVar_hsa_circ_168568,RMVar_hsa_circ_32656,RMVar_hsa_circ_366483 6918 RMVar_ID_6918 Human_SNP_ID_564918455 A-to-I Human chr14 + 91148744 91148744 91148744 AAGGCAGGAGGATCACTTGAGCTCAAGAGTTCAAGACCAGCCTTGGACAAGATAGTGAAACCTTG AAGGCAGGAGGATCACTTGAGCTCAAGAGTTCGAGACCAGCCTTGGACAAGATAGTGAAACCTTG A G DGLUCY Ensembl:ENSG00000133943 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs192799947 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39467,RMVar_hsa_circ_91919,RMVar_hsa_circ_303039,RMVar_hsa_circ_168567,RMVar_hsa_circ_168568,RMVar_hsa_circ_32656,RMVar_hsa_circ_366483 6919 RMVar_ID_6919 Human_SNP_ID_564918456 A-to-I Human chr14 + 91148747 91148747 91148747 GCAGGAGGATCACTTGAGCTCAAGAGTTCAAGACCAGCCTTGGACAAGATAGTGAAACCTTGTCT GCAGGAGGATCACTTGAGCTCAAGAGTTCAAGGCCAGCCTTGGACAAGATAGTGAAACCTTGTCT A G DGLUCY Ensembl:ENSG00000133943 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs538134303 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39467,RMVar_hsa_circ_91919,RMVar_hsa_circ_303039,RMVar_hsa_circ_168567,RMVar_hsa_circ_168568,RMVar_hsa_circ_32656,RMVar_hsa_circ_366483 6920 RMVar_ID_6920 Human_SNP_ID_564918476 A-to-I Human chr14 + 91148842 91148842 91148842 ATGGTGCAGTGTACCTGTAGTAGCAGCTACTGAGGAAGCTGAGGTAGGAGGATCGCTTGATCCCA ATGGTGCAGTGTACCTGTAGTAGCAGCTACTGCGGAAGCTGAGGTAGGAGGATCGCTTGATCCCA A C DGLUCY Ensembl:ENSG00000133943 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1405940256 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1545365 RMVar_hsa_circ_39467,RMVar_hsa_circ_91919,RMVar_hsa_circ_303039,RMVar_hsa_circ_168567,RMVar_hsa_circ_168568,RMVar_hsa_circ_32656,RMVar_hsa_circ_366483 6921 RMVar_ID_6921 Human_SNP_ID_564918477 A-to-I Human chr14 + 91148842 91148842 91148842 ATGGTGCAGTGTACCTGTAGTAGCAGCTACTGAGGAAGCTGAGGTAGGAGGATCGCTTGATCCCA ATGGTGCAGTGTACCTGTAGTAGCAGCTACTGGGGAAGCTGAGGTAGGAGGATCGCTTGATCCCA A G DGLUCY Ensembl:ENSG00000133943 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1405940256 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1545365 RMVar_hsa_circ_39467,RMVar_hsa_circ_91919,RMVar_hsa_circ_303039,RMVar_hsa_circ_168567,RMVar_hsa_circ_168568,RMVar_hsa_circ_32656,RMVar_hsa_circ_366483 6922 RMVar_ID_6922 Human_SNP_ID_564918479 A-to-I Human chr14 + 91148845 91148845 91148845 GTGCAGTGTACCTGTAGTAGCAGCTACTGAGGAAGCTGAGGTAGGAGGATCGCTTGATCCCAGGA GTGCAGTGTACCTGTAGTAGCAGCTACTGAGGGAGCTGAGGTAGGAGGATCGCTTGATCCCAGGA A G DGLUCY Ensembl:ENSG00000133943 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs577918600 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1545365 RMVar_hsa_circ_39467,RMVar_hsa_circ_91919,RMVar_hsa_circ_303039,RMVar_hsa_circ_168567,RMVar_hsa_circ_168568,RMVar_hsa_circ_32656,RMVar_hsa_circ_366483 6923 RMVar_ID_6923 Human_SNP_ID_564918523 A-to-I Human chr14 + 91148986 91148986 91148986 AAGAAAAGTAAAGGCTACGCGCGGTGGCTCATACCTGTAATTTCAGCACTTTGGGAGGCCGAGGC AAGAAAAGTAAAGGCTACGCGCGGTGGCTCATGCCTGTAATTTCAGCACTTTGGGAGGCCGAGGC A G DGLUCY Ensembl:ENSG00000133943 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1317646194 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39467,RMVar_hsa_circ_91919,RMVar_hsa_circ_303039,RMVar_hsa_circ_168567,RMVar_hsa_circ_168568,RMVar_hsa_circ_32656,RMVar_hsa_circ_366483 6924 RMVar_ID_6924 Human_SNP_ID_564921197 A-to-I Human chr14 + 91158947 91158947 91158947 GACCTCCTGGGATCAAGTGGTCCTTCCACCTCAACCTCCCAAGTAGCTAGGACTACAGGCATGCA GACCTCCTGGGATCAAGTGGTCCTTCCACCTCGACCTCCCAAGTAGCTAGGACTACAGGCATGCA A G DGLUCY Ensembl:ENSG00000133943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1389501936 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1545272 RMVar_hsa_circ_39467,RMVar_hsa_circ_91919,RMVar_hsa_circ_303039,RMVar_hsa_circ_327835,RMVar_hsa_circ_168567,RMVar_hsa_circ_168568,RMVar_hsa_circ_32656,RMVar_hsa_circ_366483,RMVar_hsa_circ_10478,RMVar_hsa_circ_320528 6925 RMVar_ID_6925 Human_SNP_ID_564923110 A-to-I Human chr14 + 91166500 91166500 91166500 CAACCTGGCCACCATAGTGAAACCCCATCCCTACTAAAAATACAAAAATTAGCTGGGCACAGTGA CAACCTGGCCACCATAGTGAAACCCCATCCCTGCTAAAAATACAAAAATTAGCTGGGCACAGTGA A G DGLUCY Ensembl:ENSG00000133943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1449768778 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39467,RMVar_hsa_circ_91919,RMVar_hsa_circ_109231,RMVar_hsa_circ_327835,RMVar_hsa_circ_168567,RMVar_hsa_circ_32656,RMVar_hsa_circ_366483,RMVar_hsa_circ_10478,RMVar_hsa_circ_168570,RMVar_hsa_circ_71387 6926 RMVar_ID_6926 Human_SNP_ID_564923943 A-to-I Human chr14 + 91169584 91169584 91169584 GCTGTGTACCACCATGCCTGGCTAGTTTTTGTATTTTTAGTATAGACGGGGTTTCACCTTGTTGC GCTGTGTACCACCATGCCTGGCTAGTTTTTGTGTTTTTAGTATAGACGGGGTTTCACCTTGTTGC A G DGLUCY Ensembl:ENSG00000133943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1209000655 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39467,RMVar_hsa_circ_32656,RMVar_hsa_circ_10478,RMVar_hsa_circ_34415,RMVar_hsa_circ_366443,RMVar_hsa_circ_340783 6927 RMVar_ID_6927 Human_SNP_ID_564923968 A-to-I Human chr14 + 91169671 91169671 91169671 AGTTCAAGTGATCTGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGTCATGAGCCACCGTGC AGTTCAAGTGATCTGCCCGCCTCGGCCTCCCAGAGTGCTGGGATTACAGTCATGAGCCACCGTGC A G DGLUCY Ensembl:ENSG00000133943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs978722392 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39467,RMVar_hsa_circ_32656,RMVar_hsa_circ_10478,RMVar_hsa_circ_34415,RMVar_hsa_circ_366443,RMVar_hsa_circ_340783 6928 RMVar_ID_6928 Human_SNP_ID_564926751 A-to-I Human chr14 + 91180099 91180099 91180099 TTTAATAGAGACAGGGTTTCACTATGTTGCCCAGGCTGGTCTTGAACTCCTGACCTCAGGTGATC TTTAATAGAGACAGGGTTTCACTATGTTGCCCGGGCTGGTCTTGAACTCCTGACCTCAGGTGATC A G DGLUCY Ensembl:ENSG00000133943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1389898111 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39467,RMVar_hsa_circ_32656,RMVar_hsa_circ_10478,RMVar_hsa_circ_366443,RMVar_hsa_circ_340783,RMVar_hsa_circ_168572,RMVar_hsa_circ_77107,RMVar_hsa_circ_329892 6929 RMVar_ID_6929 Human_SNP_ID_564926807 A-to-I Human chr14 + 91180310 91180310 91180310 AGAATAAAGTCGGGCTGGGCGTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGTCAAGAG AGAATAAAGTCGGGCTGGGCGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGTCAAGAG A G DGLUCY Ensembl:ENSG00000133943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1033298836 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39467,RMVar_hsa_circ_32656,RMVar_hsa_circ_10478,RMVar_hsa_circ_366443,RMVar_hsa_circ_340783,RMVar_hsa_circ_168572,RMVar_hsa_circ_77107,RMVar_hsa_circ_329892 6930 RMVar_ID_6930 Human_SNP_ID_564930178 A-to-I Human chr14 + 91192761 91192761 91192761 TGACAGTGGAGGTTGCAGTTAGCCAAGATCGCACCAATGCACTCCAGCCTGGGTGACAGAGTAAA TGACAGTGGAGGTTGCAGTTAGCCAAGATCGCGCCAATGCACTCCAGCCTGGGTGACAGAGTAAA A G DGLUCY Ensembl:ENSG00000133943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1295301583 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3280,RMVar_hsa_circ_32656,RMVar_hsa_circ_340783,RMVar_hsa_circ_329892,RMVar_hsa_circ_59975,RMVar_hsa_circ_294313,RMVar_hsa_circ_341560,RMVar_hsa_circ_168573 6931 RMVar_ID_6931 Human_SNP_ID_564932555 A-to-I Human chr14 + 91201479 91201479 91201479 TGCCACCACGCCCAGCTAATTTTTGTATTTTTAGTAGACATGGGGTTTCACTATGTTGGCCAGGA TGCCACCACGCCCAGCTAATTTTTGTATTTTTGGTAGACATGGGGTTTCACTATGTTGGCCAGGA A G DGLUCY Ensembl:ENSG00000133943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs558327592 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_329892,RMVar_hsa_circ_59975,RMVar_hsa_circ_341560,RMVar_hsa_circ_356404,RMVar_hsa_circ_66369,RMVar_hsa_circ_306885 6932 RMVar_ID_6932 Human_SNP_ID_564936509 A-to-I Human chr14 + 91216368 91216368 91216368 GGGGCCATTAAGAATCCCTGGTCCAGCTGGGTACGGTGACTCATGCCTATAATCTCAGCACTTTG GGGGCCATTAAGAATCCCTGGTCCAGCTGGGTGCGGTGACTCATGCCTATAATCTCAGCACTTTG A G DGLUCY Ensembl:ENSG00000133943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1285870 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1545681 RMVar_hsa_circ_66369,RMVar_hsa_circ_13697 6933 RMVar_ID_6933 Human_SNP_ID_564936569 A-to-I Human chr14 + 91216564 91216564 91216564 TACCTGGGAGGCTGAAGTGGGAGGATCGCTTGAGCCCAGGAATCCAAGGCTGCAGTGAGCTATGT TACCTGGGAGGCTGAAGTGGGAGGATCGCTTGGGCCCAGGAATCCAAGGCTGCAGTGAGCTATGT A G DGLUCY Ensembl:ENSG00000133943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs946966981 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66369,RMVar_hsa_circ_13697 6934 RMVar_ID_6934 Human_SNP_ID_564936574 A-to-I Human chr14 + 91216585 91216585 91216585 AGGATCGCTTGAGCCCAGGAATCCAAGGCTGCAGTGAGCTATGTTCACTTCACTGCACTCCAGCC AGGATCGCTTGAGCCCAGGAATCCAAGGCTGCGGTGAGCTATGTTCACTTCACTGCACTCCAGCC A G DGLUCY Ensembl:ENSG00000133943 Protein coding intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1208289576 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66369,RMVar_hsa_circ_13697 6935 RMVar_ID_6935 Human_SNP_ID_564937215 A-to-I Human chr14 + 91218695 91218695 91218695 AAAGTGCTGAGATTACAGGCGTGAGCCACCACACCTGGCCTAAAATGGGGATTTTTTAAAAGCAA AAAGTGCTGAGATTACAGGCGTGAGCCACCACGCCTGGCCTAAAATGGGGATTTTTTAAAAGCAA A G DGLUCY Ensembl:ENSG00000133943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1285864 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66369,RMVar_hsa_circ_13697 6936 RMVar_ID_6936 Human_SNP_ID_564937281 A-to-I Human chr14 + 91218930 91218930 91218930 GGCCGGGCATGGTGGCTCTCACCTGTATTCCCAGAACTTTGGGAGGCTGAGGCGGGCAGATCACT GGCCGGGCATGGTGGCTCTCACCTGTATTCCCCGAACTTTGGGAGGCTGAGGCGGGCAGATCACT A C DGLUCY Ensembl:ENSG00000133943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1243702539 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66369,RMVar_hsa_circ_13697 6937 RMVar_ID_6937 Human_SNP_ID_564937333 A-to-I Human chr14 + 91219164 91219149 91219164 ATGACACCACTGCACTCCAGCCTGGGTGACAGAGTGAGGCTCTGTCTCAAAAAAAAAAGAAAAAA ATGACACCACTGCACTCC_______________GTGAGGCTCTGTCTCAAAAAAAAAAGAAAAAA CAGCCTGGGTGACAGA C DGLUCY Ensembl:ENSG00000133943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1260494989 Functional Loss DEL dbSNP153 19..33 33 - - - RMVar_hsa_circ_66369,RMVar_hsa_circ_13697 6938 RMVar_ID_6938 Human_SNP_ID_564937335 A-to-I Human chr14 + 91219164 91219152 91219165 ATGACACCACTGCACTCCAGCCTGGGTGACAGAGTGAGGCTCTGTCTCAAAAAAAAAAGAAAAAA ATGACACCACTGCACTCCAGC_____________TGAGGCTCTGTCTCAAAAAAAAAAGAAAAAA CCTGGGTGACAGAG C DGLUCY Ensembl:ENSG00000133943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1229727463 Functional Loss DEL dbSNP153 22..34 33 - - - RMVar_hsa_circ_66369,RMVar_hsa_circ_13697 6939 RMVar_ID_6939 Human_SNP_ID_564937829 A-to-I Human chr14 + 91220947 91220947 91220947 GGCAGGAAAGAGGCTAAGGAAACGTGGGGCTCATGGTATAAACAAACACCAGGAAAGGTTTCCTG GGCAGGAAAGAGGCTAAGGAAACGTGGGGCTCGTGGTATAAACAAACACCAGGAAAGGTTTCCTG A G DGLUCY Ensembl:ENSG00000133943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1285860 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_310,GWAS_ID_311 RMVar_hsa_circ_66369,RMVar_hsa_circ_13697 6940 RMVar_ID_6940 Human_SNP_ID_564981885 A-to-I Human chr14 - 91384513 91384513 91384513 GGTGATGATTATGATGAAGAAGGTGAAGAAGCAGATGAGGAAGGGGAAGAAGGAGGAGATGAGGA GGTGATGATTATGATGAAGAAGGTGAAGAAGCGGATGAGGAAGGGGAAGAAGGAGGAGATGAGGA T C CCDC88C Ensembl:ENSG00000015133 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1349523234 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_38582,Human_RBP_ID_17067598,Human_RBP_ID_26432748 Human_Splice_Rec_1545840 RMVar_hsa_circ_49370,RMVar_hsa_circ_66874,RMVar_hsa_circ_121341,RMVar_hsa_circ_168589 6941 RMVar_ID_6941 Human_SNP_ID_565001506 A-to-I Human chr14 - 91460794 91460794 91460794 TAACGTGGTGAAACCCCGTTTCTACTAAAAATACAAAAATTAGCCAGGCGTGGTGGCGGGCGCCT TAACGTGGTGAAACCCCGTTTCTACTAAAAATCCAAAAATTAGCCAGGCGTGGTGGCGGGCGCCT T G PPP4R3A Ensembl:ENSG00000100796 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1179660228 Functional Loss SNV dbSNP153 33..33 33 - - - 6942 RMVar_ID_6942 Human_SNP_ID_565001507 A-to-I Human chr14 - 91460799 91460799 91460799 CTGGCTAACGTGGTGAAACCCCGTTTCTACTAAAAATACAAAAATTAGCCAGGCGTGGTGGCGGG CTGGCTAACGTGGTGAAACCCCGTTTCTACTACAAATACAAAAATTAGCCAGGCGTGGTGGCGGG T G PPP4R3A Ensembl:ENSG00000100796 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1382512799 Functional Loss SNV dbSNP153 33..33 33 - - - 6943 RMVar_ID_6943 Human_SNP_ID_565002092 A-to-I Human chr14 - 91462843 91462843 91462843 AGATATAAAATCATTAACTGCTCATGTAATTGAAAATTACTGGAAAGCACTGGAAGATGTAGATT AGATATAAAATCATTAACTGCTCATGTAATTGGAAATTACTGGAAAGCACTGGAAGATGTAGATT T C PPP4R3A Ensembl:ENSG00000100796 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs756118736 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1277200,Human_RBP_ID_1500883,Human_RBP_ID_1825853,Human_RBP_ID_2429565,Human_RBP_ID_17855115,Human_RBP_ID_18658681 Human_Splice_Rec_1545866,Human_Splice_Rec_1545894,Human_Splice_Rec_1545918,Human_Splice_Rec_1545930,Human_Splice_Rec_1545960,Human_Splice_Rec_1545986 Human_miRNA_ID_2843705 RMVar_hsa_circ_266801,RMVar_hsa_circ_307387,RMVar_hsa_circ_321102,RMVar_hsa_circ_96370,RMVar_hsa_circ_107702,RMVar_hsa_circ_366551,RMVar_hsa_circ_168592,RMVar_hsa_circ_344744,RMVar_hsa_circ_168593,RMVar_hsa_circ_326944,RMVar_hsa_circ_168594,RMVar_hsa_circ_58685 6944 RMVar_ID_6944 Human_SNP_ID_565002213 A-to-I Human chr14 - 91463337 91463337 91463337 TAGATAGCTGGGTGCAGTGGCTCGCACCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGCAGA TAGATAGCTGGGTGCAGTGGCTCGCACCTGTAGTCCCAGCACTTTGGGAGGCCGAGGCAGGCAGA T C PPP4R3A Ensembl:ENSG00000100796 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1453067228 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266801,RMVar_hsa_circ_321102,RMVar_hsa_circ_96370,RMVar_hsa_circ_107702,RMVar_hsa_circ_168592,RMVar_hsa_circ_344744,RMVar_hsa_circ_168593,RMVar_hsa_circ_326944,RMVar_hsa_circ_168594,RMVar_hsa_circ_58685 6945 RMVar_ID_6945 Human_SNP_ID_565002253 A-to-I Human chr14 - 91463494 91463494 91463494 AGGAGTTCAAGCCTGCAGTGAGCTATAATCATACCACTATATCTCAACCTAGGTGCCAGAACGAG AGGAGTTCAAGCCTGCAGTGAGCTATAATCATTCCACTATATCTCAACCTAGGTGCCAGAACGAG T A PPP4R3A Ensembl:ENSG00000100796 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1190049570 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17855116 RMVar_hsa_circ_266801,RMVar_hsa_circ_321102,RMVar_hsa_circ_96370,RMVar_hsa_circ_107702,RMVar_hsa_circ_168592,RMVar_hsa_circ_344744,RMVar_hsa_circ_168593,RMVar_hsa_circ_326944,RMVar_hsa_circ_168594,RMVar_hsa_circ_58685 6946 RMVar_ID_6946 Human_SNP_ID_565002399 A-to-I Human chr14 - 91464149 91464149 91464149 ACCCGACTAATTTTTGTATTTGTAGTAGAGATAGGGTCTCACTATTGGCCAGGCAGGTCTCAACC ACCCGACTAATTTTTGTATTTGTAGTAGAGATGGGGTCTCACTATTGGCCAGGCAGGTCTCAACC T C PPP4R3A Ensembl:ENSG00000100796 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs921017514 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266801,RMVar_hsa_circ_321102,RMVar_hsa_circ_96370,RMVar_hsa_circ_107702,RMVar_hsa_circ_168592,RMVar_hsa_circ_344744,RMVar_hsa_circ_168593,RMVar_hsa_circ_326944,RMVar_hsa_circ_168594,RMVar_hsa_circ_58685 6947 RMVar_ID_6947 Human_SNP_ID_565002418 A-to-I Human chr14 - 91464221 91464221 91464221 CACCTCCCAGGTTCATGCGATTCTTCTGCCTCAGCCTCTAGAGTAGCTGGGATTACAGACATGCG CACCTCCCAGGTTCATGCGATTCTTCTGCCTCGGCCTCTAGAGTAGCTGGGATTACAGACATGCG T C PPP4R3A Ensembl:ENSG00000100796 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1396892089 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266801,RMVar_hsa_circ_321102,RMVar_hsa_circ_96370,RMVar_hsa_circ_107702,RMVar_hsa_circ_168592,RMVar_hsa_circ_344744,RMVar_hsa_circ_168593,RMVar_hsa_circ_326944,RMVar_hsa_circ_168594,RMVar_hsa_circ_58685 6948 RMVar_ID_6948 Human_SNP_ID_565003831 A-to-I Human chr14 - 91469709 91469709 91469709 AAATAGAAAGCTGGGTGTGGTGGTGCACGCCTATAGTCCCAACTACTCGGGAGGCTGAGGCAGAA AAATAGAAAGCTGGGTGTGGTGGTGCACGCCTGTAGTCCCAACTACTCGGGAGGCTGAGGCAGAA T C PPP4R3A Ensembl:ENSG00000100796 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1431706014 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266801,RMVar_hsa_circ_45923,RMVar_hsa_circ_96370,RMVar_hsa_circ_107702,RMVar_hsa_circ_168592,RMVar_hsa_circ_168593,RMVar_hsa_circ_168594,RMVar_hsa_circ_58685,RMVar_hsa_circ_319132,RMVar_hsa_circ_346436,RMVar_hsa_circ_348072,RMVar_hsa_circ_308709,RMVar_hsa_circ_168595,RMVar_hsa_circ_168597,RMVar_hsa_circ_8081,RMVar_hsa_circ_168596,RMVar_hsa_circ_62539,RMVar_hsa_circ_168599 6949 RMVar_ID_6949 Human_SNP_ID_565004517 A-to-I Human chr14 - 91472592 91472592 91472592 GGCGTGGTGGCAGGTGCCTTGTGGTCCCAGCTACTGGGGAGGCTGAGGCAGGAGAATGGCGTGAA GGCGTGGTGGCAGGTGCCTTGTGGTCCCAGCTGCTGGGGAGGCTGAGGCAGGAGAATGGCGTGAA T C PPP4R3A Ensembl:ENSG00000100796 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1237448320 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266801,RMVar_hsa_circ_45923,RMVar_hsa_circ_96370,RMVar_hsa_circ_107702,RMVar_hsa_circ_168592,RMVar_hsa_circ_168593,RMVar_hsa_circ_168594,RMVar_hsa_circ_58685,RMVar_hsa_circ_319132,RMVar_hsa_circ_346436,RMVar_hsa_circ_308709,RMVar_hsa_circ_168595,RMVar_hsa_circ_8081,RMVar_hsa_circ_168596,RMVar_hsa_circ_62539,RMVar_hsa_circ_168600,RMVar_hsa_circ_317028,RMVar_hsa_circ_332951,RMVar_hsa_circ_358021,RMVar_hsa_circ_318421,RMVar_hsa_circ_23395,RMVar_hsa_circ_313249,RMVar_hsa_circ_168601 6950 RMVar_ID_6950 Human_SNP_ID_565004551 A-to-I Human chr14 - 91472741 91472741 91472741 TTCATGACAAAAATGTCCCTAAAAGGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAAGCGGA TTCATGACAAAAATGTCCCTAAAAGGCCTGTAGTCCCAGCACTTTGGGAGGCCAAGGCAAGCGGA T C PPP4R3A Ensembl:ENSG00000100796 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1325643387 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266801,RMVar_hsa_circ_45923,RMVar_hsa_circ_96370,RMVar_hsa_circ_107702,RMVar_hsa_circ_168592,RMVar_hsa_circ_168593,RMVar_hsa_circ_168594,RMVar_hsa_circ_58685,RMVar_hsa_circ_319132,RMVar_hsa_circ_346436,RMVar_hsa_circ_308709,RMVar_hsa_circ_168595,RMVar_hsa_circ_8081,RMVar_hsa_circ_168596,RMVar_hsa_circ_62539,RMVar_hsa_circ_168600,RMVar_hsa_circ_317028,RMVar_hsa_circ_332951,RMVar_hsa_circ_358021,RMVar_hsa_circ_318421,RMVar_hsa_circ_23395,RMVar_hsa_circ_313249,RMVar_hsa_circ_168601 6951 RMVar_ID_6951 Human_SNP_ID_565006195 A-to-I Human chr14 - 91479147 91479147 91479147 AAAACCTCGTCTCTACTAAAACTACAAAAATTAGCCAGGCGTGATGGTGGACACCTGTAATCCCA AAAACCTCGTCTCTACTAAAACTACAAAAATTTGCCAGGCGTGATGGTGGACACCTGTAATCCCA T A PPP4R3A Ensembl:ENSG00000100796 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1159118642 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45923,RMVar_hsa_circ_96370,RMVar_hsa_circ_168592,RMVar_hsa_circ_168594,RMVar_hsa_circ_8081,RMVar_hsa_circ_7554,RMVar_hsa_circ_168600,RMVar_hsa_circ_332951,RMVar_hsa_circ_318421,RMVar_hsa_circ_23395,RMVar_hsa_circ_168601,RMVar_hsa_circ_306621,RMVar_hsa_circ_348410,RMVar_hsa_circ_265206,RMVar_hsa_circ_40281,RMVar_hsa_circ_168603,RMVar_hsa_circ_168604,RMVar_hsa_circ_14151,RMVar_hsa_circ_314337,RMVar_hsa_circ_331213,RMVar_hsa_circ_168605 6952 RMVar_ID_6952 Human_SNP_ID_565006397 A-to-I Human chr14 - 91479680 91479680 91479680 ACAATTAGCTAAACGTGATGGTGGACGCCTGTAATCCCAGACTCGGGAGGCTGAGACGAGAGAAT ACAATTAGCTAAACGTGATGGTGGACGCCTGTGATCCCAGACTCGGGAGGCTGAGACGAGAGAAT T C PPP4R3A Ensembl:ENSG00000100796 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs543197378 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45923,RMVar_hsa_circ_96370,RMVar_hsa_circ_168592,RMVar_hsa_circ_168594,RMVar_hsa_circ_8081,RMVar_hsa_circ_7554,RMVar_hsa_circ_168600,RMVar_hsa_circ_332951,RMVar_hsa_circ_318421,RMVar_hsa_circ_23395,RMVar_hsa_circ_168601,RMVar_hsa_circ_306621,RMVar_hsa_circ_348410,RMVar_hsa_circ_265206,RMVar_hsa_circ_40281,RMVar_hsa_circ_168603,RMVar_hsa_circ_168604,RMVar_hsa_circ_14151,RMVar_hsa_circ_314337,RMVar_hsa_circ_331213,RMVar_hsa_circ_168605 6953 RMVar_ID_6953 Human_SNP_ID_565006443 A-to-I Human chr14 - 91479885 91479885 91479885 TATACCTGTAATCCCACCACTTTGGGAAGCCAAGGCAGGAGGATCGATTGAACCCAGAAGTTAAA TATACCTGTAATCCCACCACTTTGGGAAGCCACGGCAGGAGGATCGATTGAACCCAGAAGTTAAA T G PPP4R3A Ensembl:ENSG00000100796 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985228797 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45923,RMVar_hsa_circ_96370,RMVar_hsa_circ_168592,RMVar_hsa_circ_168594,RMVar_hsa_circ_8081,RMVar_hsa_circ_7554,RMVar_hsa_circ_168600,RMVar_hsa_circ_332951,RMVar_hsa_circ_318421,RMVar_hsa_circ_23395,RMVar_hsa_circ_168601,RMVar_hsa_circ_306621,RMVar_hsa_circ_348410,RMVar_hsa_circ_265206,RMVar_hsa_circ_40281,RMVar_hsa_circ_168603,RMVar_hsa_circ_168604,RMVar_hsa_circ_14151,RMVar_hsa_circ_314337,RMVar_hsa_circ_331213,RMVar_hsa_circ_168605 6954 RMVar_ID_6954 Human_SNP_ID_565006778 A-to-I Human chr14 - 91481295 91481295 91481295 TCTTGCTCTGTCACCCAGGCTGTAGGGCAATAATGCAGTCTCAGCGACTGCAACCTCCACCTTCG TCTTGCTCTGTCACCCAGGCTGTAGGGCAATAGTGCAGTCTCAGCGACTGCAACCTCCACCTTCG T C PPP4R3A Ensembl:ENSG00000100796 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs547838491 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12443080 RMVar_hsa_circ_45923,RMVar_hsa_circ_96370,RMVar_hsa_circ_168592,RMVar_hsa_circ_168594,RMVar_hsa_circ_8081,RMVar_hsa_circ_7554,RMVar_hsa_circ_168600,RMVar_hsa_circ_332951,RMVar_hsa_circ_318421,RMVar_hsa_circ_23395,RMVar_hsa_circ_168601,RMVar_hsa_circ_306621,RMVar_hsa_circ_348410,RMVar_hsa_circ_265206,RMVar_hsa_circ_40281,RMVar_hsa_circ_168603,RMVar_hsa_circ_168604,RMVar_hsa_circ_14151,RMVar_hsa_circ_314337,RMVar_hsa_circ_331213,RMVar_hsa_circ_168605 6955 RMVar_ID_6955 Human_SNP_ID_565010498 A-to-I Human chr14 - 91495439 91495435 91495440 GACTGGGAATGTGCCTGTAGTCCCAGCTACTCAGGTGGCTGAGGCAGGAGAATTGCTTGAACCCA GACTGGGAATGTGCCTGTAGTCCCAGCTACT_____GGCTGAGGCAGGAGAATTGCTTGAACCCA CACCTG C PPP4R3A Ensembl:ENSG00000100796 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1303327983 Functional Loss DEL dbSNP153 32..36 33 - - - 6956 RMVar_ID_6956 Human_SNP_ID_565010500 A-to-I Human chr14 - 91495443 91495443 91495443 TCTGGACTGGGAATGTGCCTGTAGTCCCAGCTACTCAGGTGGCTGAGGCAGGAGAATTGCTTGAA TCTGGACTGGGAATGTGCCTGTAGTCCCAGCTTCTCAGGTGGCTGAGGCAGGAGAATTGCTTGAA T A PPP4R3A Ensembl:ENSG00000100796 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs906958929 Functional Loss SNV dbSNP153 33..33 33 - - - 6957 RMVar_ID_6957 Human_SNP_ID_565010501 A-to-I Human chr14 - 91495443 91495443 91495443 TCTGGACTGGGAATGTGCCTGTAGTCCCAGCTACTCAGGTGGCTGAGGCAGGAGAATTGCTTGAA TCTGGACTGGGAATGTGCCTGTAGTCCCAGCTGCTCAGGTGGCTGAGGCAGGAGAATTGCTTGAA T C PPP4R3A Ensembl:ENSG00000100796 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs906958929 Functional Loss SNV dbSNP153 33..33 33 - - - 6958 RMVar_ID_6958 Human_SNP_ID_565011290 A-to-I Human chr14 - 91498288 91498288 91498288 CACTGTCAATTAGGCTGGAGTGCAGTGGCACAATCTTGGCTTACTGCAACCTCTGCCTCCCAGGT CACTGTCAATTAGGCTGGAGTGCAGTGGCACAGTCTTGGCTTACTGCAACCTCTGCCTCCCAGGT T C PPP4R3A Ensembl:ENSG00000100796 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs953847381 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12443339 6959 RMVar_ID_6959 Human_SNP_ID_565012033 A-to-I Human chr14 - 91500924 91500924 91500924 GGGTTCAAGCAGTCGTCCTGCCTCAGCTTCCCAAGTAGCTGGTACTACAGGCACATACCACCATG GGGTTCAAGCAGTCGTCCTGCCTCAGCTTCCCGAGTAGCTGGTACTACAGGCACATACCACCATG T C PPP4R3A Ensembl:ENSG00000100796 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs748837613 Functional Loss SNV dbSNP153 33..33 33 - - - 6960 RMVar_ID_6960 Human_SNP_ID_565012572 A-to-I Human chr14 - 91503126 91503123 91503126 GAAAATTAGCTGGGCATGTGGCACATACTTGTAGTCTTAGCTACTCAGGAGGCTGAAGCCAGAGA GAAAATTAGCTGGGCATGTGGCACATACTTGT___CTTAGCTACTCAGGAGGCTGAAGCCAGAGA GACT G PPP4R3A Ensembl:ENSG00000100796 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879519591 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_12443469 6961 RMVar_ID_6961 Human_SNP_ID_565012948 A-to-I Human chr14 - 91504485 91504485 91504485 CGATTCTCCCGCCTCAGCCTTACGAGTAGCTGACATTACAGGTGCCTGCCACCACGCCTGGTGAA CGATTCTCCCGCCTCAGCCTTACGAGTAGCTGGCATTACAGGTGCCTGCCACCACGCCTGGTGAA T C PPP4R3A Ensembl:ENSG00000100796 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10139669 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_312,GWAS_ID_313,GWAS_ID_314,GWAS_ID_315,GWAS_ID_316,GWAS_ID_317,GWAS_ID_318,GWAS_ID_319,GWAS_ID_320,GWAS_ID_321,GWAS_ID_322,GWAS_ID_323,GWAS_ID_324,GWAS_ID_325,GWAS_ID_326,GWAS_ID_327,GWAS_ID_328,GWAS_ID_329,GWAS_ID_330,GWAS_ID_331,GWAS_ID_332,GWAS_ID_333,GWAS_ID_334,GWAS_ID_335,GWAS_ID_336,GWAS_ID_337,GWAS_ID_338,GWAS_ID_339,GWAS_ID_340,GWAS_ID_341,GWAS_ID_342,GWAS_ID_343,GWAS_ID_344,GWAS_ID_345,GWAS_ID_346,GWAS_ID_347,GWAS_ID_348,GWAS_ID_349,GWAS_ID_350,GWAS_ID_351,GWAS_ID_352,GWAS_ID_353,GWAS_ID_354,GWAS_ID_355,GWAS_ID_356,GWAS_ID_357,GWAS_ID_358,GWAS_ID_359,GWAS_ID_360,GWAS_ID_361,GWAS_ID_362,GWAS_ID_363,GWAS_ID_364 6962 RMVar_ID_6962 Human_SNP_ID_565013158 A-to-I Human chr14 - 91505218 91505218 91505218 GAACTGCTGACATCAGGTGATCCGCCCTCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG GAACTGCTGACATCAGGTGATCCGCCCTCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG T C PPP4R3A Ensembl:ENSG00000100796 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1383300856 Functional Loss SNV dbSNP153 33..33 33 - - - 6963 RMVar_ID_6963 Human_SNP_ID_565013195 A-to-I Human chr14 - 91505331 91505331 91505331 ATTCTCATGCTTCAAGCCTCAAGCCTGGGATTACAGGCGTCTGCCATCATGCATGGCTAATTTTT ATTCTCATGCTTCAAGCCTCAAGCCTGGGATTTCAGGCGTCTGCCATCATGCATGGCTAATTTTT T A PPP4R3A Ensembl:ENSG00000100796 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1018065369 Functional Loss SNV dbSNP153 33..33 33 - - - 6964 RMVar_ID_6964 Human_SNP_ID_565013407 A-to-I Human chr14 - 91506084 91506084 91506084 AAATGTAGCCAGGTGTGGTGGCGGGCGCCTGTAGTCCCAGCTGCTCAGGAGGCTGAGGCAGGAGA AAATGTAGCCAGGTGTGGTGGCGGGCGCCTGTGGTCCCAGCTGCTCAGGAGGCTGAGGCAGGAGA T C PPP4R3A Ensembl:ENSG00000100796 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs139109577 Functional Loss SNV dbSNP153 33..33 33 - - - 6965 RMVar_ID_6965 Human_SNP_ID_565013472 A-to-I Human chr14 - 91506352 91506352 91506352 TTCTTACAACAGTGTCTGATTTAGTGCTATTAACCATATTAAACTCCCATGTTACTGTCTACTTG TTCTTACAACAGTGTCTGATTTAGTGCTATTAGCCATATTAAACTCCCATGTTACTGTCTACTTG T C PPP4R3A Ensembl:ENSG00000100796 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2180886 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_365,GWAS_ID_366,GWAS_ID_367,GWAS_ID_368,GWAS_ID_369,GWAS_ID_370,GWAS_ID_371,GWAS_ID_372,GWAS_ID_373,GWAS_ID_374,GWAS_ID_375,GWAS_ID_376,GWAS_ID_377,GWAS_ID_378,GWAS_ID_379,GWAS_ID_380,GWAS_ID_381,GWAS_ID_382,GWAS_ID_383,GWAS_ID_384,GWAS_ID_385,GWAS_ID_386,GWAS_ID_387,GWAS_ID_388,GWAS_ID_389,GWAS_ID_390,GWAS_ID_391,GWAS_ID_392,GWAS_ID_393,GWAS_ID_394,GWAS_ID_395,GWAS_ID_396,GWAS_ID_397,GWAS_ID_398,GWAS_ID_399,GWAS_ID_400,GWAS_ID_401,GWAS_ID_402,GWAS_ID_403,GWAS_ID_404,GWAS_ID_405,GWAS_ID_406,GWAS_ID_407,GWAS_ID_408,GWAS_ID_409,GWAS_ID_410,GWAS_ID_411,GWAS_ID_412,GWAS_ID_413,GWAS_ID_414,GWAS_ID_415,GWAS_ID_416,GWAS_ID_417 6966 RMVar_ID_6966 Human_SNP_ID_565013582 A-to-I Human chr14 - 91506738 91506738 91506738 CAAGACCAGCCTGGGCAACATGGCGAAACCCCATCTCTACAAAACATACAAACATTAGCTGGTGC CAAGACCAGCCTGGGCAACATGGCGAAACCCCGTCTCTACAAAACATACAAACATTAGCTGGTGC T C PPP4R3A Ensembl:ENSG00000100796 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs56125230 Functional Loss SNV dbSNP153 33..33 33 - - - 6967 RMVar_ID_6967 Human_SNP_ID_565013603 A-to-I Human chr14 - 91506825 91506825 91506825 TGGACTTAGGCTGGGTGCGGTGGCTCACGCCTATAATCCCAGCATTTTGGGATGCCCAGGCCGAC TGGACTTAGGCTGGGTGCGGTGGCTCACGCCTGTAATCCCAGCATTTTGGGATGCCCAGGCCGAC T C PPP4R3A Ensembl:ENSG00000100796 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs955840444 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17562620 6968 RMVar_ID_6968 Human_SNP_ID_565078631 A-to-I Human chr14 - 91779052 91779052 91779052 TATTTTTTTTTAAGTAGAGACAGGATTTTGCCATGTTTGCCAGGTTGGCCTTGAACTCCTGACCT TATTTTTTTTTAAGTAGAGACAGGATTTTGCCGTGTTTGCCAGGTTGGCCTTGAACTCCTGACCT T C CATSPERB Ensembl:ENSG00000133962 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1322854912 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1546132,Human_Splice_Rec_1546133 6969 RMVar_ID_6969 Human_SNP_ID_565100637 A-to-I Human chr14 - 91876994 91876994 91876994 TACAAAAAAAAAAGTTAGCCGGTCATGGTGGCAGGCACCTGTAGTCTCAGCTACCTGGGGCAGTG TACAAAAAAAAAAGTTAGCCGGTCATGGTGGCGGGCACCTGTAGTCTCAGCTACCTGGGGCAGTG T C FBLN5 Ensembl:ENSG00000140092 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1046827518 Functional Loss SNV dbSNP153 33..33 33 - - - 6970 RMVar_ID_6970 Human_SNP_ID_565100648 A-to-I Human chr14 - 91877039 91877039 91877039 CAGGAGCTCAAGACCAGCTTGGGCAACATGGCAAAACTCTGTCTCTACAAAAAAAAAAGTTAGCC CAGGAGCTCAAGACCAGCTTGGGCAACATGGCGAAACTCTGTCTCTACAAAAAAAAAAGTTAGCC T C FBLN5 Ensembl:ENSG00000140092 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1434073433 Functional Loss SNV dbSNP153 33..33 33 - - - 6971 RMVar_ID_6971 Human_SNP_ID_565101150 A-to-I Human chr14 - 91878997 91878997 91878997 CAGCTCATTGAAGCCTCAACCTTTTGGGCTCAAACAATCGTCCTGCCTCAGCCTTTTAAGTAGCT CAGCTCATTGAAGCCTCAACCTTTTGGGCTCAGACAATCGTCCTGCCTCAGCCTTTTAAGTAGCT T C FBLN5 Ensembl:ENSG00000140092 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1246265632 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_365710 6972 RMVar_ID_6972 Human_SNP_ID_565114786 A-to-I Human chr14 + 91933465 91933465 91933465 CCCAACTAATTTTTGTATTTTTAGGGGGTTTCATCATGTTGGCCAGGCTGGTCTCGAACTCCTGA CCCAACTAATTTTTGTATTTTTAGGGGGTTTCGTCATGTTGGCCAGGCTGGTCTCGAACTCCTGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879049855 Functional Loss SNV dbSNP153 33..33 33 - - - 6973 RMVar_ID_6973 Human_SNP_ID_565139098 A-to-I Human chr14 - 92032285 92032285 92032285 AAATTAGCTGGATGTGGTGGTGCACACCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAC AAATTAGCTGGATGTGGTGGTGCACACCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAC T C TRIP11 Ensembl:ENSG00000100815 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1025812321 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69375,RMVar_hsa_circ_18509,RMVar_hsa_circ_11530,RMVar_hsa_circ_273572,RMVar_hsa_circ_77561,RMVar_hsa_circ_168641,RMVar_hsa_circ_168642,RMVar_hsa_circ_23926,RMVar_hsa_circ_283588,RMVar_hsa_circ_21117,RMVar_hsa_circ_298196 6974 RMVar_ID_6974 Human_SNP_ID_565139734 A-to-I Human chr14 - 92034728 92034728 92034728 CTTGGAAGGCTGAAGCGAGAGAGTTTGAGGCTACAGTGAGCCATGATCACACCACTATACTCCAG CTTGGAAGGCTGAAGCGAGAGAGTTTGAGGCTGCAGTGAGCCATGATCACACCACTATACTCCAG T C TRIP11 Ensembl:ENSG00000100815 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1338439289 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77561,RMVar_hsa_circ_168642 6975 RMVar_ID_6975 Human_SNP_ID_565139751 A-to-I Human chr14 - 92034800 92034800 92034800 GTGAAACCTCATCTCTCCAAAAAAGTAAAAAAATTAGGTAGGTGTGGTCGCATGTGCCTGTAGTT GTGAAACCTCATCTCTCCAAAAAAGTAAAAAACTTAGGTAGGTGTGGTCGCATGTGCCTGTAGTT T G TRIP11 Ensembl:ENSG00000100815 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1186410208 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77561,RMVar_hsa_circ_168642 6976 RMVar_ID_6976 Human_SNP_ID_565144475 A-to-I Human chr14 - 92054075 92054075 92054075 AAAAATTAGCCAGGCGTGGTTGGTGTGCGCCTATTATGCCAGCTACTTGGGAGGCTGATGCAGGA AAAAATTAGCCAGGCGTGGTTGGTGTGCGCCTGTTATGCCAGCTACTTGGGAGGCTGATGCAGGA T C ATXN3 Ensembl:ENSG00000066427 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256433694 Functional Loss SNV dbSNP153 33..33 33 - - - 6977 RMVar_ID_6977 Human_SNP_ID_565145788 A-to-I Human chr14 - 92059604 92059604 92059604 CCATGTTAGGCTGGTCTCAAACTCCTGACCTCAGGTGATCTGCCTGCCTTGGCCTCCCAAAGTGC CCATGTTAGGCTGGTCTCAAACTCCTGACCTCGGGTGATCTGCCTGCCTTGGCCTCCCAAAGTGC T C ATXN3 Ensembl:ENSG00000066427 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1004396548 Functional Loss SNV dbSNP153 33..33 33 - - - 6978 RMVar_ID_6978 Human_SNP_ID_565145790 A-to-I Human chr14 - 92059616 92059616 92059616 GACGGGCTTTTACCATGTTAGGCTGGTCTCAAACTCCTGACCTCAGGTGATCTGCCTGCCTTGGC GACGGGCTTTTACCATGTTAGGCTGGTCTCAAGCTCCTGACCTCAGGTGATCTGCCTGCCTTGGC T C ATXN3 Ensembl:ENSG00000066427 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1304736828 Functional Loss SNV dbSNP153 33..33 33 - - - 6979 RMVar_ID_6979 Human_SNP_ID_565145815 A-to-I Human chr14 - 92059690 92059690 92059690 CCTCAGCCTCCCAAGTACCTGGGATTACAGGCACCTGCCACTACACCTGGCGAATATTTGTTTTT CCTCAGCCTCCCAAGTACCTGGGATTACAGGCCCCTGCCACTACACCTGGCGAATATTTGTTTTT T G ATXN3 Ensembl:ENSG00000066427 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs969266308 Functional Loss SNV dbSNP153 33..33 33 - - - 6980 RMVar_ID_6980 Human_SNP_ID_565145900 A-to-I Human chr14 - 92059961 92059961 92059961 AACCCAGGAGGTGGAGGTTGCAGTGAGCTGAGATCGTGCCATTGCACTCTAGCCTGGGCAACAAG AACCCAGGAGGTGGAGGTTGCAGTGAGCTGAGCTCGTGCCATTGCACTCTAGCCTGGGCAACAAG T G ATXN3 Ensembl:ENSG00000066427 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1464007062 Functional Loss SNV dbSNP153 33..33 33 - - - 6981 RMVar_ID_6981 Human_SNP_ID_565145916 A-to-I Human chr14 - 92060040 92060029 92060040 ATACAAAACTTAAGCCAGGTATGGTGGCGGGCACCTGTAATCCCAGTTACTTGGGAGGCTGAGGC ATACAAAACTTAAGCCAGGTATGGTGGCGGGC___________CAGTTACTTGGGAGGCTGAGGC GGGATTACAGGT G ATXN3 Ensembl:ENSG00000066427 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs974492777 Functional Loss DEL dbSNP153 33..43 33 - - - 6982 RMVar_ID_6982 Human_SNP_ID_565145919 A-to-I Human chr14 - 92060040 92060040 92060040 ATACAAAACTTAAGCCAGGTATGGTGGCGGGCACCTGTAATCCCAGTTACTTGGGAGGCTGAGGC ATACAAAACTTAAGCCAGGTATGGTGGCGGGCCCCTGTAATCCCAGTTACTTGGGAGGCTGAGGC T G ATXN3 Ensembl:ENSG00000066427 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1197892053 Functional Loss SNV dbSNP153 33..33 33 - - - 6983 RMVar_ID_6983 Human_SNP_ID_565146235 A-to-I Human chr14 - 92060870 92060870 92060870 AAATTAGCTGGGCGCGGTGGCAGGTGCCTGTAATCCCAGCTACCTGGGAGTCTGAGGCAGGAGAA AAATTAGCTGGGCGCGGTGGCAGGTGCCTGTAGTCCCAGCTACCTGGGAGTCTGAGGCAGGAGAA T C ATXN3 Ensembl:ENSG00000066427 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs3178662 Functional Loss SNV dbSNP153 33..33 33 - - - 6984 RMVar_ID_6984 Human_SNP_ID_565146278 A-to-I Human chr14 - 92061004 92061004 92061004 GTGGCGGCTGGGCGTGGTAGCTCACGCCTGTAATCCCAGCATTTTGGGAGGCCGAAGTGGGTGGA GTGGCGGCTGGGCGTGGTAGCTCACGCCTGTATTCCCAGCATTTTGGGAGGCCGAAGTGGGTGGA T A ATXN3 Ensembl:ENSG00000066427 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1331880597 Functional Loss SNV dbSNP153 33..33 33 - - - 6985 RMVar_ID_6985 Human_SNP_ID_565146528 A-to-I Human chr14 - 92062197 92062197 92062197 GCTGGAGGGCAGTGGCATGATCTCGGCTCACTACAACTTCCACCTCCCGGGTTCAAGCAATTCTC GCTGGAGGGCAGTGGCATGATCTCGGCTCACTGCAACTTCCACCTCCCGGGTTCAAGCAATTCTC T C ATXN3 Ensembl:ENSG00000066427 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs766144891 Functional Loss SNV dbSNP153 33..33 33 - - - 6986 RMVar_ID_6986 Human_SNP_ID_565148457 A-to-I Human chr14 - 92070390 92070390 92070390 TATTTTTAGTAGAGACAGGGTTTCACCATGTTAGCCAGGATGGTCTCAATCTCCTGACCTCATGA TATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGATGGTCTCAATCTCCTGACCTCATGA T C ATXN3 Ensembl:ENSG00000066427 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1225173833 Functional Loss SNV dbSNP153 33..33 33 - - - 6987 RMVar_ID_6987 Human_SNP_ID_565148460 A-to-I Human chr14 - 92070406 92070406 92070406 CCTGGCTAATTTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTAGCCAGGATGGTCTCAA CCTGGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTAGCCAGGATGGTCTCAA T C ATXN3 Ensembl:ENSG00000066427 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1213763885 Functional Loss SNV dbSNP153 33..33 33 - - - 6988 RMVar_ID_6988 Human_SNP_ID_565148461 A-to-I Human chr14 - 92070412 92070412 92070412 ACATCGCCTGGCTAATTTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTAGCCAGGATGG ACATCGCCTGGCTAATTTTTTGTATTTTTAGTGGAGACAGGGTTTCACCATGTTAGCCAGGATGG T C ATXN3 Ensembl:ENSG00000066427 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1278447207 Functional Loss SNV dbSNP153 33..33 33 - - - 6989 RMVar_ID_6989 Human_SNP_ID_565149965 A-to-I Human chr14 - 92075267 92075267 92075267 CTAGCTATTTGGCAGGCTGAGGCAGGAGAATCACTTGAACCTGGGAGGCAGAGGTTGCAGTGAGC CTAGCTATTTGGCAGGCTGAGGCAGGAGAATCGCTTGAACCTGGGAGGCAGAGGTTGCAGTGAGC T C ATXN3 Ensembl:ENSG00000066427 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs758405707 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25119295 RMVar_hsa_circ_15777,RMVar_hsa_circ_301964,RMVar_hsa_circ_317302,RMVar_hsa_circ_358909,RMVar_hsa_circ_346759,RMVar_hsa_circ_313362,RMVar_hsa_circ_286081,RMVar_hsa_circ_115259,RMVar_hsa_circ_168646,RMVar_hsa_circ_168648,RMVar_hsa_circ_168650,RMVar_hsa_circ_9543,RMVar_hsa_circ_168649,RMVar_hsa_circ_168647,RMVar_hsa_circ_168645 6990 RMVar_ID_6990 Human_SNP_ID_565161286 A-to-I Human chr14 - 92117747 92117747 92117747 GTGATCTGCCCACCTCAGCATCCCAAAGTGCTAGGATTACAGGCATGAACCACCGCACCTGGCCC GTGATCTGCCCACCTCAGCATCCCAAAGTGCTGGGATTACAGGCATGAACCACCGCACCTGGCCC T C NDUFB1 Ensembl:ENSG00000183648 Protein coding intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1461218281 Functional Loss SNV dbSNP153 33..33 33 - - - 6991 RMVar_ID_6991 Human_SNP_ID_565161292 A-to-I Human chr14 - 92117763 92117763 92117763 GAACTCCTAATCTCAAGTGATCTGCCCACCTCAGCATCCCAAAGTGCTAGGATTACAGGCATGAA GAACTCCTAATCTCAAGTGATCTGCCCACCTCCGCATCCCAAAGTGCTAGGATTACAGGCATGAA T G NDUFB1 Ensembl:ENSG00000183648 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1460020949 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25119415 6992 RMVar_ID_6992 Human_SNP_ID_565161300 A-to-I Human chr14 - 92117832 92117832 92117832 CACCACACCCGGCTAATTTTTGTGCTTTTAGTAGAAATGGGGTTTTGCCATGTTGGCCAGGCTGG CACCACACCCGGCTAATTTTTGTGCTTTTAGTGGAAATGGGGTTTTGCCATGTTGGCCAGGCTGG T C NDUFB1 Ensembl:ENSG00000183648 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs759282538 Functional Loss SNV dbSNP153 33..33 33 - - - 6993 RMVar_ID_6993 Human_SNP_ID_565161515 A-to-I Human chr14 - 92118811 92118811 92118811 TGCCACTACGCCCACCTAATTTTTGTATTTTTAGTAGAGATGGAGTTTCACCATGTTGGCCAGGC TGCCACTACGCCCACCTAATTTTTGTATTTTTGGTAGAGATGGAGTTTCACCATGTTGGCCAGGC T C NDUFB1 Ensembl:ENSG00000183648 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1012239319 Functional Loss SNV dbSNP153 33..33 33 - - - 6994 RMVar_ID_6994 Human_SNP_ID_565161532 A-to-I Human chr14 - 92118887 92118887 92118887 TCACTGCAACCTCTGCCTCCCGAGTTCAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAACTGGGA TCACTGCAACCTCTGCCTCCCGAGTTCAAGCAGTTCTCCTGCCTCAGCCTCCTGAGTAACTGGGA T C NDUFB1 Ensembl:ENSG00000183648 Protein coding 5'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1383703608 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1547226 6995 RMVar_ID_6995 Human_SNP_ID_565161625 A-to-I Human chr14 - 92119124 92119121 92119124 GATTTTTTGTAGAGACAGGGTTTTGCCATGTTAACCAGGCTAGTCTCAAGCTCCTAGGCTCAAGC GATTTTTTGTAGAGACAGGGTTTTGCCATGTT___CAGGCTAGTCTCAAGCTCCTAGGCTCAAGC GGTT G NDUFB1 Ensembl:ENSG00000183648 Protein coding intron GSE38233;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;esophageal squamous carcinoma cells,EC109 cell line - 24183664,32596459 RNA-Seq:(High) rs1351519151 Functional Loss DEL dbSNP153 33..35 33 - - - 6996 RMVar_ID_6996 Human_SNP_ID_565161648 A-to-I Human chr14 - 92119212 92119212 92119212 CGTCTCTTGGGCTCAAGCAATCCTCCCACCTCAGCCTCCGAAGTAGCTGGGACTACAGGCATATA CGTCTCTTGGGCTCAAGCAATCCTCCCACCTCGGCCTCCGAAGTAGCTGGGACTACAGGCATATA T C NDUFB1 Ensembl:ENSG00000183648 Protein coding intron GSE38233;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,32596459 RNA-Seq:(High) rs1353037300 Functional Loss SNV dbSNP153 33..33 33 - - - 6997 RMVar_ID_6997 Human_SNP_ID_565161649 A-to-I Human chr14 - 92119225 92119225 92119225 TCATTGCAACCTCCGTCTCTTGGGCTCAAGCAATCCTCCCACCTCAGCCTCCGAAGTAGCTGGGA TCATTGCAACCTCCGTCTCTTGGGCTCAAGCATTCCTCCCACCTCAGCCTCCGAAGTAGCTGGGA T A NDUFB1 Ensembl:ENSG00000183648 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1256232199 Functional Loss SNV dbSNP153 33..33 33 - - - 6998 RMVar_ID_6998 Human_SNP_ID_565161650 A-to-I Human chr14 - 92119225 92119225 92119225 TCATTGCAACCTCCGTCTCTTGGGCTCAAGCAATCCTCCCACCTCAGCCTCCGAAGTAGCTGGGA TCATTGCAACCTCCGTCTCTTGGGCTCAAGCAGTCCTCCCACCTCAGCCTCCGAAGTAGCTGGGA T C NDUFB1 Ensembl:ENSG00000183648 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1256232199 Functional Loss SNV dbSNP153 33..33 33 - - - 6999 RMVar_ID_6999 Human_SNP_ID_565161673 A-to-I Human chr14 - 92119276 92119276 92119276 ACAGCATCACGCTCTGTCGTCCAGGCTAGAGTACAGTGGTGTGATCTCAGGTCATTGCAACCTCC ACAGCATCACGCTCTGTCGTCCAGGCTAGAGTCCAGTGGTGTGATCTCAGGTCATTGCAACCTCC T G NDUFB1 Ensembl:ENSG00000183648 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs1269628179 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12472077 7000 RMVar_ID_7000 Human_SNP_ID_565161674 A-to-I Human chr14 - 92119281 92119281 92119281 TTGAGACAGCATCACGCTCTGTCGTCCAGGCTAGAGTACAGTGGTGTGATCTCAGGTCATTGCAA TTGAGACAGCATCACGCTCTGTCGTCCAGGCTGGAGTACAGTGGTGTGATCTCAGGTCATTGCAA T C NDUFB1 Ensembl:ENSG00000183648 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs1224438791 Functional Loss SNV dbSNP153 33..33 33 - - - 7001 RMVar_ID_7001 Human_SNP_ID_565161684 A-to-I Human chr14 - 92119306 92119306 92119306 TAACCTAGTAGTCTTTTTTTTTTTTTTGAGACAGCATCACGCTCTGTCGTCCAGGCTAGAGTACA TAACCTAGTAGTCTTTTTTTTTTTTTTGAGACGGCATCACGCTCTGTCGTCCAGGCTAGAGTACA T C NDUFB1 Ensembl:ENSG00000183648 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1286169871 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12472078 7002 RMVar_ID_7002 Human_SNP_ID_565161846 A-to-I Human chr14 - 92119854 92119854 92119854 AGAAGATTGAGGTGGGAAGATCACTTGAGCTCAGGAGTTCAAGACTGCAGTGGACTATTATAACT AGAAGATTGAGGTGGGAAGATCACTTGAGCTCGGGAGTTCAAGACTGCAGTGGACTATTATAACT T C NDUFB1 Ensembl:ENSG00000183648 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1312073748 Functional Loss SNV dbSNP153 33..33 33 - - - 7003 RMVar_ID_7003 Human_SNP_ID_565161848 A-to-I Human chr14 - 92119883 92119880 92119883 TAAATTAGCACCCGTAGCTCCAGCTTCTCAGAAGATTGAGGTGGGAAGATCACTTGAGCTCAGGA TAAATTAGCACCCGTAGCTCCAGCTTCTCAGA___TTGAGGTGGGAAGATCACTTGAGCTCAGGA ATCT A NDUFB1 Ensembl:ENSG00000183648 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 31158229,32596459,32596459 RNA-Seq:(High) rs1335507321 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_276612,Human_RBP_ID_17562621 7004 RMVar_ID_7004 Human_SNP_ID_565162023 A-to-I Human chr14 - 92120495 92120494 92120496 AAATACAAAATTAGCTGGGCATGGTGGCGCATACCTGTAATCCCAGCTACTTGGGAGGCTGAGGT AAATACAAAATTAGCTGGGCATGGTGGCGCA__CCTGTAATCCCAGCTACTTGGGAGGCTGAGGT GTA G NDUFB1 Ensembl:ENSG00000183648 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1232565373 Functional Loss DEL dbSNP153 32..33 33 - - - 7005 RMVar_ID_7005 Human_SNP_ID_565162055 A-to-I Human chr14 - 92120573 92120573 92120573 GGCCTAGGCGGGCGGACCACCTGAGGTTGGGAATTCAAGACCAGCCTGACCAACATGGAGAAACC GGCCTAGGCGGGCGGACCACCTGAGGTTGGGAGTTCAAGACCAGCCTGACCAACATGGAGAAACC T C NDUFB1 Ensembl:ENSG00000183648 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1279147017 Functional Loss SNV dbSNP153 33..33 33 - - - 7006 RMVar_ID_7006 Human_SNP_ID_565162132 A-to-I Human chr14 - 92120738 92120738 92120738 ACCAGCCCGGCCAACAGTGAAACCCCATCTCTACTTAAAAATACAAAAATTAGCCGGGCGTGGTG ACCAGCCCGGCCAACAGTGAAACCCCATCTCTGCTTAAAAATACAAAAATTAGCCGGGCGTGGTG T C NDUFB1 Ensembl:ENSG00000183648 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs751007457 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23161277 7007 RMVar_ID_7007 Human_SNP_ID_565162147 A-to-I Human chr14 - 92120788 92120788 92120788 CAACACTTTGGAAGGCCGAGGTGGCCGGATCAAGAGGTCAGGAGTTTGAGACCAGCCCGGCCAAC CAACACTTTGGAAGGCCGAGGTGGCCGGATCACGAGGTCAGGAGTTTGAGACCAGCCCGGCCAAC T G NDUFB1 Ensembl:ENSG00000183648 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1352074899 Functional Loss SNV dbSNP153 33..33 33 - - - 7008 RMVar_ID_7008 Human_SNP_ID_565162148 A-to-I Human chr14 - 92120789 92120789 92120789 CCAACACTTTGGAAGGCCGAGGTGGCCGGATCAAGAGGTCAGGAGTTTGAGACCAGCCCGGCCAA CCAACACTTTGGAAGGCCGAGGTGGCCGGATCGAGAGGTCAGGAGTTTGAGACCAGCCCGGCCAA T C NDUFB1 Ensembl:ENSG00000183648 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1053699299 Functional Loss SNV dbSNP153 33..33 33 - - - 7009 RMVar_ID_7009 Human_SNP_ID_565162218 A-to-I Human chr14 - 92120995 92120995 92120995 ACCACACCCGGCTAATTTTTTGTATATTTAGTAGAGACGAGGGTTTCACTATGTTGGCCAGGCTG ACCACACCCGGCTAATTTTTTGTATATTTAGTGGAGACGAGGGTTTCACTATGTTGGCCAGGCTG T C NDUFB1 Ensembl:ENSG00000183648 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1480789630 Functional Loss SNV dbSNP153 33..33 33 - - - 7010 RMVar_ID_7010 Human_SNP_ID_565162236 A-to-I Human chr14 - 92121079 92121067 92121080 CGGCTCACTCCAACCTCCGCCTCCCGGGTTCAAGCGATTCTCCCGTCTCAGCAGCCCAAGTAGCT CGGCTCACTCCAACCTCCGCCTCCCGGGTTC_____________GTCTCAGCAGCCCAAGTAGCT CGGGAGAATCGCTT C NDUFB1 Ensembl:ENSG00000183648 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1421218854 Functional Loss DEL dbSNP153 32..44 33 - - - 7011 RMVar_ID_7011 Human_SNP_ID_565164938 A-to-I Human chr14 + 92131619 92131619 92131619 CCAGTACTTTAGGAGGCTGAGGTGGGCAGATCACTTGAGTTCAGGAGTTCGAGACCAGCCTGGCC CCAGTACTTTAGGAGGCTGAGGTGGGCAGATCCCTTGAGTTCAGGAGTTCGAGACCAGCCTGGCC A C CPSF2 Ensembl:ENSG00000165934 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1567017000 Functional Loss SNV dbSNP153 33..33 33 - - - 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_269781,RMVar_hsa_circ_39866,RMVar_hsa_circ_323754,RMVar_hsa_circ_168663,RMVar_hsa_circ_348244,RMVar_hsa_circ_311703,RMVar_hsa_circ_168665 7012 RMVar_ID_7012 Human_SNP_ID_565165103 A-to-I Human chr14 + 92132260 92132260 92132260 GGGTTCAAGTTATTCTCCTTCCTCAGCCTCCCAAGTAGCTGAGATTACAGGCATGCACCACCCGG GGGTTCAAGTTATTCTCCTTCCTCAGCCTCCCGAGTAGCTGAGATTACAGGCATGCACCACCCGG A G CPSF2 Ensembl:ENSG00000165934 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1255046667 Functional Loss SNV dbSNP153 33..33 33 - - - 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_269781,RMVar_hsa_circ_39866,RMVar_hsa_circ_323754,RMVar_hsa_circ_168663,RMVar_hsa_circ_348244,RMVar_hsa_circ_311703,RMVar_hsa_circ_168665 7013 RMVar_ID_7013 Human_SNP_ID_565165122 A-to-I Human chr14 + 92132318 92132318 92132318 CACCCGGCCGGCTAAGTTTTTGTATTTTTAGTAGAAACAGGGTTTCACCATATTAGCCAGACTGG CACCCGGCCGGCTAAGTTTTTGTATTTTTAGTGGAAACAGGGTTTCACCATATTAGCCAGACTGG A G CPSF2 Ensembl:ENSG00000165934 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1255065582 Functional Loss SNV dbSNP153 33..33 33 - - - 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_269781,RMVar_hsa_circ_39866,RMVar_hsa_circ_323754,RMVar_hsa_circ_168663,RMVar_hsa_circ_348244,RMVar_hsa_circ_311703,RMVar_hsa_circ_168665 7014 RMVar_ID_7014 Human_SNP_ID_565167292 A-to-I Human chr14 + 92140771 92140771 92140771 CCATCTCTACAAAAAAAAAGAAAATTTTTGCCAGACGTGGTGGTACAGGCCCGTAGTTCCAGCTG CCATCTCTACAAAAAAAAAGAAAATTTTTGCCGGACGTGGTGGTACAGGCCCGTAGTTCCAGCTG A G CPSF2 Ensembl:ENSG00000165934 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1028065962 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_168661,RMVar_hsa_circ_90785,RMVar_hsa_circ_50899,RMVar_hsa_circ_281926,RMVar_hsa_circ_269781,RMVar_hsa_circ_22196,RMVar_hsa_circ_168668,RMVar_hsa_circ_93595,RMVar_hsa_circ_168663,RMVar_hsa_circ_348244,RMVar_hsa_circ_311703,RMVar_hsa_circ_109255,RMVar_hsa_circ_76585,RMVar_hsa_circ_78326,RMVar_hsa_circ_168669,RMVar_hsa_circ_56232,RMVar_hsa_circ_168666,RMVar_hsa_circ_168667,RMVar_hsa_circ_87654,RMVar_hsa_circ_32618,RMVar_hsa_circ_43166,RMVar_hsa_circ_27918,RMVar_hsa_circ_168673 7015 RMVar_ID_7015 Human_SNP_ID_565167300 A-to-I Human chr14 + 92140793 92140793 92140793 AATTTTTGCCAGACGTGGTGGTACAGGCCCGTAGTTCCAGCTGCTTGGGAGGCTGGGGTGGGAGG AATTTTTGCCAGACGTGGTGGTACAGGCCCGTGGTTCCAGCTGCTTGGGAGGCTGGGGTGGGAGG A G CPSF2 Ensembl:ENSG00000165934 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1386158810 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_168661,RMVar_hsa_circ_90785,RMVar_hsa_circ_50899,RMVar_hsa_circ_281926,RMVar_hsa_circ_269781,RMVar_hsa_circ_22196,RMVar_hsa_circ_168668,RMVar_hsa_circ_93595,RMVar_hsa_circ_168663,RMVar_hsa_circ_348244,RMVar_hsa_circ_311703,RMVar_hsa_circ_109255,RMVar_hsa_circ_76585,RMVar_hsa_circ_78326,RMVar_hsa_circ_168669,RMVar_hsa_circ_56232,RMVar_hsa_circ_168666,RMVar_hsa_circ_168667,RMVar_hsa_circ_87654,RMVar_hsa_circ_32618,RMVar_hsa_circ_43166,RMVar_hsa_circ_27918,RMVar_hsa_circ_168673 7016 RMVar_ID_7016 Human_SNP_ID_565169850 A-to-I Human chr14 + 92151759 92151759 92151759 ATTTGCAAAAATATAGAATAATGCTATAGGCCAGGTGCGGTGGCTCATGACTGTAATCCCAGCAC ATTTGCAAAAATATAGAATAATGCTATAGGCCCGGTGCGGTGGCTCATGACTGTAATCCCAGCAC A C CPSF2 Ensembl:ENSG00000165934 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1372318082 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_168661,RMVar_hsa_circ_90785,RMVar_hsa_circ_50899,RMVar_hsa_circ_168668,RMVar_hsa_circ_93595,RMVar_hsa_circ_348244,RMVar_hsa_circ_109255,RMVar_hsa_circ_76585,RMVar_hsa_circ_78326,RMVar_hsa_circ_168669,RMVar_hsa_circ_56232,RMVar_hsa_circ_168666,RMVar_hsa_circ_168667,RMVar_hsa_circ_87654,RMVar_hsa_circ_32618,RMVar_hsa_circ_27918,RMVar_hsa_circ_60018,RMVar_hsa_circ_168673,RMVar_hsa_circ_360097,RMVar_hsa_circ_353540,RMVar_hsa_circ_273515,RMVar_hsa_circ_168676,RMVar_hsa_circ_168675 7017 RMVar_ID_7017 Human_SNP_ID_565174328 A-to-I Human chr14 + 92169951 92169946 92169951 CTTGAGCTCAGGAGTTTGAGACCAACCTGGGCAACATAGTGAGAACTCATCTCTATTAAAAATCA CTTGAGCTCAGGAGTTTGAGACCAACCT_____ACATAGTGAGAACTCATCTCTATTAAAAATCA TGGGCA T CPSF2 Ensembl:ENSG00000165934 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1009992038 Functional Loss DEL dbSNP153 29..33 33 - - - Human_RBP_ID_12444995 7018 RMVar_ID_7018 Human_SNP_ID_565174334 A-to-I Human chr14 + 92169973 92169973 92169973 CAACCTGGGCAACATAGTGAGAACTCATCTCTATTAAAAATCAGAAAAATTGGCCAGGTGTGGTG CAACCTGGGCAACATAGTGAGAACTCATCTCTCTTAAAAATCAGAAAAATTGGCCAGGTGTGGTG A C CPSF2 Ensembl:ENSG00000165934 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs996052484 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12444995 7019 RMVar_ID_7019 Human_SNP_ID_565221375 A-to-I Human chr14 + 92361930 92361930 92361930 GGAACCTGGATATGGCATCTCAAAGGGGAGGCAAAGACAGCACCTTGGGAAACACCCTATTCTGG GGAACCTGGATATGGCATCTCAAAGGGGAGGCGAAGACAGCACCTTGGGAAACACCCTATTCTGG A G SLC24A4 Ensembl:ENSG00000140090 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1481293922 Functional Loss SNV dbSNP153 33..33 33 - - - 7020 RMVar_ID_7020 Human_SNP_ID_565269271 A-to-I Human chr14 - 92555945 92555942 92555945 AGTGGGAGACGCCCCCACTCACCCCAGCCACCACCCGGTGCAGGATCCTGGCCACCTCTGCCTGG AGTGGGAGACGCCCCCACTCACCCCAGCCACC___CGGTGCAGGATCCTGGCCACCTCTGCCTGG GGGT G - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs760845110 Functional Loss DEL dbSNP153 33..35 33 - - - 7021 RMVar_ID_7021 Human_SNP_ID_565306613 A-to-I Human chr14 - 92705879 92705879 92705879 TCATGTCTGCAATCCCAGCACGTTGGGAGGCCAAGGTGGGTGGCTCACCTGAAGTCAGGAGTTCC TCATGTCTGCAATCCCAGCACGTTGGGAGGCCGAGGTGGGTGGCTCACCTGAAGTCAGGAGTTCC T C LGMN Ensembl:ENSG00000100600 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1053482237 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107561,RMVar_hsa_circ_168684 7022 RMVar_ID_7022 Human_SNP_ID_565316036 A-to-I Human chr14 - 92742554 92742554 92742554 GGCTGGGTGCAGTGGCTCACATCTGTAATCCCAGCACTTTGGGAGGCTAAGGCAGGTGCATCACT GGCTGGGTGCAGTGGCTCACATCTGTAATCCCCGCACTTTGGGAGGCTAAGGCAGGTGCATCACT T G LGMN Ensembl:ENSG00000100600 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1042706392 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96704,RMVar_hsa_circ_168690 7023 RMVar_ID_7023 Human_SNP_ID_565363392 A-to-I Human chr14 + 92932734 92932731 92932734 TACGGCTTCAGGGGCCCTGGGCCGCAGCTGCGACGAGGCTGGAGGCCATCCTCCCGGGAGGACAG TACGGCTTCAGGGGCCCTGGGCCGCAGCTG___CGAGGCTGGAGGCCATCCTCCCGGGAGGACAG GCGA G CHGA Ensembl:ENSG00000100604 Protein coding CDS GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs757076345 Functional Loss DEL dbSNP153 31..33 33 - - - 7024 RMVar_ID_7024 Human_SNP_ID_565397946 A-to-I Human chr14 - 93072711 93072711 93072711 CCGCTTGGGGCTGAGGTGGGAGGATCACTTGAACCCAGGAGGTCGAGGCTGCAGTGAACTGAGAT CCGCTTGGGGCTGAGGTGGGAGGATCACTTGAGCCCAGGAGGTCGAGGCTGCAGTGAACTGAGAT T C ITPK1 Ensembl:ENSG00000100605 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1257089897 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82381,RMVar_hsa_circ_168714,RMVar_hsa_circ_328829,RMVar_hsa_circ_168715 7025 RMVar_ID_7025 Human_SNP_ID_565397947 A-to-I Human chr14 - 93072717 93072717 93072717 GTATGACCGCTTGGGGCTGAGGTGGGAGGATCACTTGAACCCAGGAGGTCGAGGCTGCAGTGAAC GTATGACCGCTTGGGGCTGAGGTGGGAGGATCGCTTGAACCCAGGAGGTCGAGGCTGCAGTGAAC T C ITPK1 Ensembl:ENSG00000100605 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474245557 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82381,RMVar_hsa_circ_168714,RMVar_hsa_circ_328829,RMVar_hsa_circ_168715 7026 RMVar_ID_7026 Human_SNP_ID_565428540 A-to-I Human chr14 - 93182847 93182847 93182847 TGGCTCACTGCATCCTCCGCCTTCCAGGTTTAAGCTATTCTCCTGCCTCAGTTGCCCGAGTAGCT TGGCTCACTGCATCCTCCGCCTTCCAGGTTTAGGCTATTCTCCTGCCTCAGTTGCCCGAGTAGCT T C MOAP1 Ensembl:ENSG00000165943 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1035119902 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4305899,Human_RBP_ID_18658977 Human_miRNA_ID_575061 7027 RMVar_ID_7027 Human_SNP_ID_565433821 A-to-I Human chr14 - 93202935 93202935 93202935 CCTCCTGTAGCCATACTTTGATTTTGCTTTAAAAAGATTATTGAATCCTTTTAAAAATATATATT CCTCCTGTAGCCATACTTTGATTTTGCTTTAACAAGATTATTGAATCCTTTTAAAAATATATATT T G GON7 Ensembl:ENSG00000170270 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1179626431 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_453854,Human_RBP_ID_1501181 7028 RMVar_ID_7028 Human_SNP_ID_565444870 A-to-I Human chr14 - 93245121 93245121 93245121 GCCATGACTCACACCTGTAATCCCAACACTTTAGGAGGCTGAAGTGGGAGGATCACTTGAGCCCA GCCATGACTCACACCTGTAATCCCAACACTTTGGGAGGCTGAAGTGGGAGGATCACTTGAGCCCA T C BTBD7 Ensembl:ENSG00000011114 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444464381 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106641,RMVar_hsa_circ_110334,RMVar_hsa_circ_168727,RMVar_hsa_circ_168729,RMVar_hsa_circ_94171,RMVar_hsa_circ_168728 7029 RMVar_ID_7029 Human_SNP_ID_565446632 A-to-I Human chr14 - 93252224 93252224 93252224 CTTACTACAACCTTCTCCTCCCGAGTTCAAGCAGTTCTCGTGCCTCAGCCTCCTGAGTAGCTGGG CTTACTACAACCTTCTCCTCCCGAGTTCAAGCGGTTCTCGTGCCTCAGCCTCCTGAGTAGCTGGG T C BTBD7 Ensembl:ENSG00000011114 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348748506 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106641,RMVar_hsa_circ_168727,RMVar_hsa_circ_94171,RMVar_hsa_circ_168728,RMVar_hsa_circ_122664,RMVar_hsa_circ_264930,RMVar_hsa_circ_57358,RMVar_hsa_circ_168730,RMVar_hsa_circ_342667,RMVar_hsa_circ_168732 7030 RMVar_ID_7030 Human_SNP_ID_565450830 A-to-I Human chr14 - 93270471 93270471 93270471 CTAGGCTTGTCTCGAACTCCTGACCTCGGGTAATCTACCTGCCTCAGCCTCTTAAAGTGTGGGAT CTAGGCTTGTCTCGAACTCCTGACCTCGGGTAGTCTACCTGCCTCAGCCTCTTAAAGTGTGGGAT T C BTBD7 Ensembl:ENSG00000011114 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1033156441 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106641,RMVar_hsa_circ_168727,RMVar_hsa_circ_168735,RMVar_hsa_circ_335723,RMVar_hsa_circ_317187,RMVar_hsa_circ_168739,RMVar_hsa_circ_339866,RMVar_hsa_circ_168736 7031 RMVar_ID_7031 Human_SNP_ID_565496145 A-to-I Human chr14 + 93462191 93462191 93462191 AGCCAGATGTGGTGACCGGCACCTGTAATCCCAGCTACTGGCAGGGCTCAGGCAGGAGAATCACG AGCCAGATGTGGTGACCGGCACCTGTAATCCCGGCTACTGGCAGGGCTCAGGCAGGAGAATCACG A G UNC79 Ensembl:ENSG00000133958 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs888169170 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_168745 7032 RMVar_ID_7032 Human_SNP_ID_565496146 A-to-I Human chr14 + 93462191 93462191 93462191 AGCCAGATGTGGTGACCGGCACCTGTAATCCCAGCTACTGGCAGGGCTCAGGCAGGAGAATCACG AGCCAGATGTGGTGACCGGCACCTGTAATCCCTGCTACTGGCAGGGCTCAGGCAGGAGAATCACG A T UNC79 Ensembl:ENSG00000133958 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs888169170 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_168745 7033 RMVar_ID_7033 Human_SNP_ID_565640302 A-to-I Human chr14 - 94053259 94053259 94053259 CAAGGAGGTTGAGGCTGCAGTGAGCCATGATCATGCCACTGCTCTCCAGCCTGGGCAGCAGAGTG CAAGGAGGTTGAGGCTGCAGTGAGCCATGATCTTGCCACTGCTCTCCAGCCTGGGCAGCAGAGTG T A DDX24 Ensembl:ENSG00000089737 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1016426252 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94544,RMVar_hsa_circ_120930,RMVar_hsa_circ_168812,RMVar_hsa_circ_168813 7034 RMVar_ID_7034 Human_SNP_ID_565640303 A-to-I Human chr14 - 94053259 94053259 94053259 CAAGGAGGTTGAGGCTGCAGTGAGCCATGATCATGCCACTGCTCTCCAGCCTGGGCAGCAGAGTG CAAGGAGGTTGAGGCTGCAGTGAGCCATGATCGTGCCACTGCTCTCCAGCCTGGGCAGCAGAGTG T C DDX24 Ensembl:ENSG00000089737 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1016426252 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94544,RMVar_hsa_circ_120930,RMVar_hsa_circ_168812,RMVar_hsa_circ_168813 7035 RMVar_ID_7035 Human_SNP_ID_565645275 A-to-I Human chr14 - 94072682 94072682 94072682 TGAACTACAGGCATGTGCCACCATGCCCGGCTACTTTTTGCATTTTTAGTAGAGACAGGGTTTCA TGAACTACAGGCATGTGCCACCATGCCCGGCTCCTTTTTGCATTTTTAGTAGAGACAGGGTTTCA T G DDX24 Ensembl:ENSG00000089737 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1365775997 Functional Loss SNV dbSNP153 33..33 33 - - - 7036 RMVar_ID_7036 Human_SNP_ID_565651739 A-to-I Human chr14 + 94098286 94098286 94098286 GCCCTTCAGGAGAATGTTCCATGCCACTCCCTAGTTTCTGGTGGCTGCTGTCAGTCTTCGACGTC GCCCTTCAGGAGAATGTTCCATGCCACTCCCTGGTTTCTGGTGGCTGCTGTCAGTCTTCGACGTC A G IFI27L1 Ensembl:ENSG00000165948 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1487713000 Functional Loss SNV dbSNP153 33..33 33 - - - 7037 RMVar_ID_7037 Human_SNP_ID_565659061 A-to-I Human chr14 - 94127874 94127871 94127874 TCTTCTCTCCCAGCTGAACCCGAGGCTAAAGAAGATGAGGCAAGAGAAAATGTACCCCAAGGTGA TCTTCTCTCCCAGCTGAACCCGAGGCTAAAGA___TGAGGCAAGAGAAAATGTACCCCAAGGTGA ATCT A IFI27L2 Ensembl:ENSG00000119632 Protein coding exon GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs751140047 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_118164,RMVar_hsa_circ_122174,RMVar_hsa_circ_118619,RMVar_hsa_circ_168817,RMVar_hsa_circ_168818,RMVar_hsa_circ_168819 7038 RMVar_ID_7038 Human_SNP_ID_565912578 A-to-I Human chr14 - 95095993 95095993 95095993 CTGTATTGAAAGACTCGGAATATGGTTGTTTGAAGATTCCACCAAGATGTATGTTTGATCATCCA CTGTATTGAAAGACTCGGAATATGGTTGTTTGGAGATTCCACCAAGATGTATGTTTGATCATCCA T C DICER1 Ensembl:ENSG00000100697 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991814398 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1501516,Human_RBP_ID_1826453,Human_RBP_ID_8797583,Human_RBP_ID_27648883 RMVar_hsa_circ_96636,RMVar_hsa_circ_122457,RMVar_hsa_circ_113315,RMVar_hsa_circ_105806,RMVar_hsa_circ_168830,RMVar_hsa_circ_168832,RMVar_hsa_circ_93536,RMVar_hsa_circ_168833,RMVar_hsa_circ_168831,RMVar_hsa_circ_168829,RMVar_hsa_circ_69216,RMVar_hsa_circ_24293,RMVar_hsa_circ_81178,RMVar_hsa_circ_168835,RMVar_hsa_circ_117005,RMVar_hsa_circ_46406,RMVar_hsa_circ_168836 7039 RMVar_ID_7039 Human_SNP_ID_566207361 A-to-I Human chr14 + 96262650 96262649 96262651 TTTTTTTTTGTTGTTGTTGTTGTTGTTGAGACAGGGTCTCAGTCCGTCGGCCCAGACTGAAGTGC TTTTTTTTTGTTGTTGTTGTTGTTGTTGAGAC__GGTCTCAGTCCGTCGGCCCAGACTGAAGTGC CAG C AL355102.2,BDKRB1 Ensembl:ENSG00000258691,Ensembl:ENSG00000100739 Protein coding,Protein coding intron,intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1260602224 Functional Loss DEL dbSNP153 33..34 33 - - - 7040 RMVar_ID_7040 Human_SNP_ID_566226639 A-to-I Human chr14 - 96339355 96339355 96339355 TGTATATACACCACATACATATATATGTGTGTATATATATGTTTGTGTATATATGTGTATATATG TGTATATACACCACATACATATATATGTGTGTGTATATATGTTTGTGTATATATGTGTATATATG T C ATG2B Ensembl:ENSG00000066739 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs531362062 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_373964,RMVar_hsa_circ_124156,RMVar_hsa_circ_168859,RMVar_hsa_circ_168860,RMVar_hsa_circ_33979,RMVar_hsa_circ_68643,RMVar_hsa_circ_106700,RMVar_hsa_circ_266298,RMVar_hsa_circ_168869,RMVar_hsa_circ_84046,RMVar_hsa_circ_168873,RMVar_hsa_circ_351938,RMVar_hsa_circ_126729,RMVar_hsa_circ_72818,RMVar_hsa_circ_168878,RMVar_hsa_circ_168879,RMVar_hsa_circ_370812,RMVar_hsa_circ_329818,RMVar_hsa_circ_362803,RMVar_hsa_circ_53405,RMVar_hsa_circ_92376,RMVar_hsa_circ_168880,RMVar_hsa_circ_27163,RMVar_hsa_circ_168884,RMVar_hsa_circ_16240,RMVar_hsa_circ_168885 7041 RMVar_ID_7041 Human_SNP_ID_566273172 A-to-I Human chr14 + 96522484 96522482 96522484 CCAGACTGGAGTGCAGTGGCATGATCTTAGCTAACTGTATCCTCCACCTCCCGGGCTCAGGCAAT CCAGACTGGAGTGCAGTGGCATGATCTTAGC__ACTGTATCCTCCACCTCCCGGGCTCAGGCAAT CTA C PAPOLA Ensembl:ENSG00000090060 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1353108016 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_12451696 RMVar_hsa_circ_168896,RMVar_hsa_circ_276529,RMVar_hsa_circ_297411,RMVar_hsa_circ_321239,RMVar_hsa_circ_368207,RMVar_hsa_circ_301955,RMVar_hsa_circ_290528,RMVar_hsa_circ_113309,RMVar_hsa_circ_272413,RMVar_hsa_circ_270026,RMVar_hsa_circ_90362,RMVar_hsa_circ_168897,RMVar_hsa_circ_65420,RMVar_hsa_circ_168892,RMVar_hsa_circ_168894,RMVar_hsa_circ_168895,RMVar_hsa_circ_168893,RMVar_hsa_circ_168890,RMVar_hsa_circ_168891,RMVar_hsa_circ_168889 7042 RMVar_ID_7042 Human_SNP_ID_566273725 A-to-I Human chr14 + 96524570 96524570 96524570 TTTTGAGACAGGGTCTGACTGTCGCCCAGGCTAGAGTGCAGTGGCGTGATCATGGCTCACGTAGC TTTTGAGACAGGGTCTGACTGTCGCCCAGGCTTGAGTGCAGTGGCGTGATCATGGCTCACGTAGC A T PAPOLA Ensembl:ENSG00000090060 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1050707262 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18936992 RMVar_hsa_circ_168896,RMVar_hsa_circ_276529,RMVar_hsa_circ_297411,RMVar_hsa_circ_321239,RMVar_hsa_circ_368207,RMVar_hsa_circ_301955,RMVar_hsa_circ_290528,RMVar_hsa_circ_113309,RMVar_hsa_circ_272413,RMVar_hsa_circ_270026,RMVar_hsa_circ_90362,RMVar_hsa_circ_168897,RMVar_hsa_circ_65420,RMVar_hsa_circ_168892,RMVar_hsa_circ_168894,RMVar_hsa_circ_168895,RMVar_hsa_circ_168893,RMVar_hsa_circ_168890,RMVar_hsa_circ_168891,RMVar_hsa_circ_168889 7043 RMVar_ID_7043 Human_SNP_ID_566273743 A-to-I Human chr14 + 96524633 96524633 96524633 GCCTTGACCTGTAGGACTCAAGCAATCCTCCCACCTTAGCCACCTGATTAGCTGGGACTATATGT GCCTTGACCTGTAGGACTCAAGCAATCCTCCCTCCTTAGCCACCTGATTAGCTGGGACTATATGT A T PAPOLA Ensembl:ENSG00000090060 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1261323621 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12451722 RMVar_hsa_circ_168896,RMVar_hsa_circ_276529,RMVar_hsa_circ_297411,RMVar_hsa_circ_321239,RMVar_hsa_circ_368207,RMVar_hsa_circ_301955,RMVar_hsa_circ_290528,RMVar_hsa_circ_113309,RMVar_hsa_circ_272413,RMVar_hsa_circ_270026,RMVar_hsa_circ_90362,RMVar_hsa_circ_168897,RMVar_hsa_circ_65420,RMVar_hsa_circ_168892,RMVar_hsa_circ_168894,RMVar_hsa_circ_168895,RMVar_hsa_circ_168893,RMVar_hsa_circ_168890,RMVar_hsa_circ_168891,RMVar_hsa_circ_168889 7044 RMVar_ID_7044 Human_SNP_ID_566275229 A-to-I Human chr14 + 96530527 96530527 96530527 TCCTACCTCAGCCCCCCCAAGTAGGTGGGACTACAGGCGCTTGTCACCATGCCTGGCTAATTTTT TCCTACCTCAGCCCCCCCAAGTAGGTGGGACTGCAGGCGCTTGTCACCATGCCTGGCTAATTTTT A G PAPOLA Ensembl:ENSG00000090060 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs994152616 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12451882 RMVar_hsa_circ_276529,RMVar_hsa_circ_321239,RMVar_hsa_circ_368207,RMVar_hsa_circ_301955,RMVar_hsa_circ_290528,RMVar_hsa_circ_113309,RMVar_hsa_circ_270026,RMVar_hsa_circ_90362,RMVar_hsa_circ_168892,RMVar_hsa_circ_168894,RMVar_hsa_circ_168895,RMVar_hsa_circ_168893,RMVar_hsa_circ_168890,RMVar_hsa_circ_168891,RMVar_hsa_circ_168889,RMVar_hsa_circ_45063,RMVar_hsa_circ_52202,RMVar_hsa_circ_324131,RMVar_hsa_circ_168900,RMVar_hsa_circ_55250,RMVar_hsa_circ_36520 7045 RMVar_ID_7045 Human_SNP_ID_566275298 A-to-I Human chr14 + 96530845 96530845 96530845 GTTTTTGTTTTGCTGTTTTGAGTCAGGGTTTTACTCCTGTCACCCAGGCTGGAGTGCGGTGGCAT GTTTTTGTTTTGCTGTTTTGAGTCAGGGTTTTGCTCCTGTCACCCAGGCTGGAGTGCGGTGGCAT A G PAPOLA Ensembl:ENSG00000090060 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1209553439 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12451895 RMVar_hsa_circ_276529,RMVar_hsa_circ_321239,RMVar_hsa_circ_368207,RMVar_hsa_circ_301955,RMVar_hsa_circ_290528,RMVar_hsa_circ_113309,RMVar_hsa_circ_270026,RMVar_hsa_circ_90362,RMVar_hsa_circ_168892,RMVar_hsa_circ_168894,RMVar_hsa_circ_168895,RMVar_hsa_circ_168893,RMVar_hsa_circ_168890,RMVar_hsa_circ_168891,RMVar_hsa_circ_168889,RMVar_hsa_circ_45063,RMVar_hsa_circ_52202,RMVar_hsa_circ_324131,RMVar_hsa_circ_168900,RMVar_hsa_circ_55250,RMVar_hsa_circ_36520 7046 RMVar_ID_7046 Human_SNP_ID_566275326 A-to-I Human chr14 + 96530908 96530908 96530908 ATGGTTTTGACTTACCGCAACCTCCGCCTTCCAGGCTCAAATGATTTTTCTGCCTCAGCCTCCCA ATGGTTTTGACTTACCGCAACCTCCGCCTTCCTGGCTCAAATGATTTTTCTGCCTCAGCCTCCCA A T PAPOLA Ensembl:ENSG00000090060 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1225311366 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_276529,RMVar_hsa_circ_321239,RMVar_hsa_circ_368207,RMVar_hsa_circ_301955,RMVar_hsa_circ_290528,RMVar_hsa_circ_113309,RMVar_hsa_circ_270026,RMVar_hsa_circ_90362,RMVar_hsa_circ_168892,RMVar_hsa_circ_168894,RMVar_hsa_circ_168895,RMVar_hsa_circ_168893,RMVar_hsa_circ_168890,RMVar_hsa_circ_168891,RMVar_hsa_circ_168889,RMVar_hsa_circ_45063,RMVar_hsa_circ_52202,RMVar_hsa_circ_324131,RMVar_hsa_circ_168900,RMVar_hsa_circ_55250,RMVar_hsa_circ_36520 7047 RMVar_ID_7047 Human_SNP_ID_566275343 A-to-I Human chr14 + 96530989 96530989 96530989 CCATAGCTGAGACCACAGGTGTGTGCCACTACACCTGGCTAATTTTTTTGTAGTTTTTGTTTTTG CCATAGCTGAGACCACAGGTGTGTGCCACTACCCCTGGCTAATTTTTTTGTAGTTTTTGTTTTTG A C PAPOLA Ensembl:ENSG00000090060 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs923427408 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18659535 RMVar_hsa_circ_276529,RMVar_hsa_circ_321239,RMVar_hsa_circ_368207,RMVar_hsa_circ_301955,RMVar_hsa_circ_290528,RMVar_hsa_circ_113309,RMVar_hsa_circ_270026,RMVar_hsa_circ_90362,RMVar_hsa_circ_168892,RMVar_hsa_circ_168894,RMVar_hsa_circ_168895,RMVar_hsa_circ_168893,RMVar_hsa_circ_168890,RMVar_hsa_circ_168891,RMVar_hsa_circ_168889,RMVar_hsa_circ_45063,RMVar_hsa_circ_52202,RMVar_hsa_circ_324131,RMVar_hsa_circ_168900,RMVar_hsa_circ_55250,RMVar_hsa_circ_36520 7048 RMVar_ID_7048 Human_SNP_ID_566275344 A-to-I Human chr14 + 96530989 96530989 96530989 CCATAGCTGAGACCACAGGTGTGTGCCACTACACCTGGCTAATTTTTTTGTAGTTTTTGTTTTTG CCATAGCTGAGACCACAGGTGTGTGCCACTACGCCTGGCTAATTTTTTTGTAGTTTTTGTTTTTG A G PAPOLA Ensembl:ENSG00000090060 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs923427408 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18659535 RMVar_hsa_circ_276529,RMVar_hsa_circ_321239,RMVar_hsa_circ_368207,RMVar_hsa_circ_301955,RMVar_hsa_circ_290528,RMVar_hsa_circ_113309,RMVar_hsa_circ_270026,RMVar_hsa_circ_90362,RMVar_hsa_circ_168892,RMVar_hsa_circ_168894,RMVar_hsa_circ_168895,RMVar_hsa_circ_168893,RMVar_hsa_circ_168890,RMVar_hsa_circ_168891,RMVar_hsa_circ_168889,RMVar_hsa_circ_45063,RMVar_hsa_circ_52202,RMVar_hsa_circ_324131,RMVar_hsa_circ_168900,RMVar_hsa_circ_55250,RMVar_hsa_circ_36520 7049 RMVar_ID_7049 Human_SNP_ID_567061571 A-to-I Human chr14 - 99511447 99511447 99511447 AAGGAGTCTCATTTGTAACCAAGATGGAATTCACAGTATGTTGTTACATTCACACTTAAAAAATA AAGGAGTCTCATTTGTAACCAAGATGGAATTCGCAGTATGTTGTTACATTCACACTTAAAAAATA T C CCDC85C Ensembl:ENSG00000205476 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1038834353 Functional Loss SNV dbSNP153 33..33 33 - - - 7050 RMVar_ID_7050 Human_SNP_ID_567088079 A-to-I Human chr14 + 99613400 99613400 99613400 CAGGCTGGAGTGCAGTGGTGCCATCTCGGCTCACCACAGCCTCGACCTCCTGGGCTCAAGCAATT CAGGCTGGAGTGCAGTGGTGCCATCTCGGCTCGCCACAGCCTCGACCTCCTGGGCTCAAGCAATT A G AL160313.2 Ensembl:ENSG00000247970 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1368007807 Functional Loss SNV dbSNP153 33..33 33 - - - 7051 RMVar_ID_7051 Human_SNP_ID_567147450 A-to-I Human chr14 + 99846005 99846005 99846005 CCAGGAGGCGGCGGTTGCAGTGAGCTGAGATCACGCCACTGCACTCCAGCCTGGGCAATAGAGCA CCAGGAGGCGGCGGTTGCAGTGAGCTGAGATCGCGCCACTGCACTCCAGCCTGGGCAATAGAGCA A G EML1 Ensembl:ENSG00000066629 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs370654398 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110014,RMVar_hsa_circ_168974,RMVar_hsa_circ_168973,RMVar_hsa_circ_168975 7052 RMVar_ID_7052 Human_SNP_ID_567169939 A-to-I Human chr14 - 99940330 99940330 99940330 TAATGTAAACGTTGCAACCTTGTTGGTATTCAATGTGCACTGTGTCATATATTGTACAACAAAAG TAATGTAAACGTTGCAACCTTGTTGGTATTCAGTGTGCACTGTGTCATATATTGTACAACAAAAG T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs575168570 Functional Loss SNV dbSNP153 33..33 33 - - - 7053 RMVar_ID_7053 Human_SNP_ID_567250331 A-to-I Human chr14 + 100245072 100245072 100245072 CATTCTCCTGCCTCAGCCTCCAGAGTAGCTGGAACTACAGGCGCCCGCTGCCACACCCGGCTAAT CATTCTCCTGCCTCAGCCTCCAGAGTAGCTGGGACTACAGGCGCCCGCTGCCACACCCGGCTAAT A G YY1 Ensembl:ENSG00000100811 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1018663367 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90088,RMVar_hsa_circ_169021 7054 RMVar_ID_7054 Human_SNP_ID_567253122 A-to-I Human chr14 + 100254544 100254544 100254544 CAGTGGTGCAATTTCAGCTTACTGCAAACTCTACCTCCCAGGTTCAAGCGGTTCTTTTGCCTCAG CAGTGGTGCAATTTCAGCTTACTGCAAACTCTGCCTCCCAGGTTCAAGCGGTTCTTTTGCCTCAG A G YY1 Ensembl:ENSG00000100811 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1004976573 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90088,RMVar_hsa_circ_169021 7055 RMVar_ID_7055 Human_SNP_ID_567255740 A-to-I Human chr14 + 100264126 100264126 100264126 GCCTCAAGTGATCCTCCTGCCTCGGTCTCTCAAATTGTTGGGATGACAGGTATGAGCCACTGCAC GCCTCAAGTGATCCTCCTGCCTCGGTCTCTCAGATTGTTGGGATGACAGGTATGAGCCACTGCAC A G YY1,AL157871.5 Ensembl:ENSG00000100811,Ensembl:ENSG00000258904 Protein coding,lincRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs954677651 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12266255 RMVar_hsa_circ_24801,RMVar_hsa_circ_90088,RMVar_hsa_circ_169021,RMVar_hsa_circ_313465,RMVar_hsa_circ_103268,RMVar_hsa_circ_169023 7056 RMVar_ID_7056 Human_SNP_ID_567255776 A-to-I Human chr14 + 100264289 100264289 100264289 ACCCCCACCTCCTGGGTTCAAGCGATTCTCCTACCTCAGCCCCCCAAGTAGCTGGGATTACAGGT ACCCCCACCTCCTGGGTTCAAGCGATTCTCCTGCCTCAGCCCCCCAAGTAGCTGGGATTACAGGT A G YY1,AL157871.5 Ensembl:ENSG00000100811,Ensembl:ENSG00000258904 Protein coding,lincRNA intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1209495534 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24801,RMVar_hsa_circ_90088,RMVar_hsa_circ_169021,RMVar_hsa_circ_313465,RMVar_hsa_circ_103268,RMVar_hsa_circ_169023 7057 RMVar_ID_7057 Human_SNP_ID_567255799 A-to-I Human chr14 + 100264377 100264377 100264377 TTTTGTGTTTTTAGTAGAGACGGAGTTTCACCATGTTGGCCAGCCTGGTCTCGAACTCCTGACCT TTTTGTGTTTTTAGTAGAGACGGAGTTTCACCGTGTTGGCCAGCCTGGTCTCGAACTCCTGACCT A G YY1,AL157871.5 Ensembl:ENSG00000100811,Ensembl:ENSG00000258904 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1455364781 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24801,RMVar_hsa_circ_90088,RMVar_hsa_circ_169021,RMVar_hsa_circ_313465,RMVar_hsa_circ_103268,RMVar_hsa_circ_169023 7058 RMVar_ID_7058 Human_SNP_ID_567255808 A-to-I Human chr14 + 100264410 100264410 100264410 TGTTGGCCAGCCTGGTCTCGAACTCCTGACCTAAAGTGATCCACCCACCTTGGCTTCCCAAAATG TGTTGGCCAGCCTGGTCTCGAACTCCTGACCTGAAGTGATCCACCCACCTTGGCTTCCCAAAATG A G YY1,AL157871.5 Ensembl:ENSG00000100811,Ensembl:ENSG00000258904 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs949872156 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23160141 RMVar_hsa_circ_24801,RMVar_hsa_circ_90088,RMVar_hsa_circ_169021,RMVar_hsa_circ_313465,RMVar_hsa_circ_103268,RMVar_hsa_circ_169023 7059 RMVar_ID_7059 Human_SNP_ID_567257760 A-to-I Human chr14 + 100271818 100271818 100271818 AGGCATGTGCCACCACGCCTGGCTAACTTTTTATTTTTTTTAGAGACGGGGTGTTGCTTTCTTGC AGGCATGTGCCACCACGCCTGGCTAACTTTTTTTTTTTTTTAGAGACGGGGTGTTGCTTTCTTGC A T YY1 Ensembl:ENSG00000100811 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1029516288 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6322832,Human_RBP_ID_12266578 RMVar_hsa_circ_24801,RMVar_hsa_circ_90088,RMVar_hsa_circ_169021,RMVar_hsa_circ_313465,RMVar_hsa_circ_103268,RMVar_hsa_circ_169023 7060 RMVar_ID_7060 Human_SNP_ID_567258274 A-to-I Human chr14 + 100273428 100273428 100273428 TACTGCCTTCGGCTTCCCGAGTGGTTGGGACTATCGACACACACCACCATGCCTGGCTGATTTTG TACTGCCTTCGGCTTCCCGAGTGGTTGGGACTGTCGACACACACCACCATGCCTGGCTGATTTTG A G YY1 Ensembl:ENSG00000100811 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs755622069 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6322868,Human_RBP_ID_12266639 RMVar_hsa_circ_24801,RMVar_hsa_circ_90088,RMVar_hsa_circ_169021,RMVar_hsa_circ_313465,RMVar_hsa_circ_103268,RMVar_hsa_circ_169023 7061 RMVar_ID_7061 Human_SNP_ID_567264594 A-to-I Human chr14 - 100296377 100296377 100296377 TCACCCTAGGTGGAGTGCAGTGGTGCAATCATAGCCCACTGCAGCCTTGATTTCCCAGGCTCAAG TCACCCTAGGTGGAGTGCAGTGGTGCAATCATGGCCCACTGCAGCCTTGATTTCCCAGGCTCAAG T C SLC25A29 Ensembl:ENSG00000197119 Protein coding 5'UTR GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,29796672,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs1254715143 Functional Loss SNV dbSNP153 33..33 33 - - - 7062 RMVar_ID_7062 Human_SNP_ID_567264652 A-to-I Human chr14 - 100296582 100296582 100296582 AAAAGAAAAAAGAAGGAAAGTGCACACATCCTAGGTGTACAAGTCGTCGCAAAACACATGCGTGG AAAAGAAAAAAGAAGGAAAGTGCACACATCCTGGGTGTACAAGTCGTCGCAAAACACATGCGTGG T C SLC25A29 Ensembl:ENSG00000197119 Protein coding intron GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs959860120 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2404450 7063 RMVar_ID_7063 Human_SNP_ID_567264671 A-to-I Human chr14 - 100296631 100296631 100296631 TCGCGTCACTGCACTCCAGCCTGGGCAACGGAATGAGACTCCGTCTCAAAAAAGAAAAAAGAAGG TCGCGTCACTGCACTCCAGCCTGGGCAACGGAGTGAGACTCCGTCTCAAAAAAGAAAAAAGAAGG T C SLC25A29 Ensembl:ENSG00000197119 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs530221120 Functional Loss SNV dbSNP153 33..33 33 - - - 7064 RMVar_ID_7064 Human_SNP_ID_567264687 A-to-I Human chr14 - 100296667 100296667 100296667 GTGAATCCGGGAGGCGGAGCTTGCAGTGAGCCAAGATCGCGTCACTGCACTCCAGCCTGGGCAAC GTGAATCCGGGAGGCGGAGCTTGCAGTGAGCCGAGATCGCGTCACTGCACTCCAGCCTGGGCAAC T C SLC25A29 Ensembl:ENSG00000197119 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs879697204 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25124488 7065 RMVar_ID_7065 Human_SNP_ID_567264771 A-to-I Human chr14 - 100296887 100296887 100296887 CATATAGAAAGTGCACACATCCTGGCCAGGCTAGTGGCTCATGCCTGTAATCCCAGCACTTCTGG CATATAGAAAGTGCACACATCCTGGCCAGGCTGGTGGCTCATGCCTGTAATCCCAGCACTTCTGG T C SLC25A29 Ensembl:ENSG00000197119 Protein coding intron GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1467831108 Functional Loss SNV dbSNP153 33..33 33 - - - 7066 RMVar_ID_7066 Human_SNP_ID_567264803 A-to-I Human chr14 - 100296994 100296994 100296994 CAAGTGATTCTCCTGCCTCGGTTCCCCCCCCAACCCCCTGGGTAGCTGGGATTACAGGCACGTGC CAAGTGATTCTCCTGCCTCGGTTCCCCCCCCAGCCCCCTGGGTAGCTGGGATTACAGGCACGTGC T C SLC25A29 Ensembl:ENSG00000197119 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs575292726 Functional Loss SNV dbSNP153 33..33 33 - - - 7067 RMVar_ID_7067 Human_SNP_ID_567264815 A-to-I Human chr14 - 100297024 100297024 100297024 TGGCTTACTGCAACTTCTTCCTCCTGGGTTCAAGTGATTCTCCTGCCTCGGTTCCCCCCCCAACC TGGCTTACTGCAACTTCTTCCTCCTGGGTTCAGGTGATTCTCCTGCCTCGGTTCCCCCCCCAACC T C SLC25A29 Ensembl:ENSG00000197119 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 29129909,30559470 RNA-Seq:(High) rs1485907416 Functional Loss SNV dbSNP153 33..33 33 - - - 7068 RMVar_ID_7068 Human_SNP_ID_567265712 A-to-I Human chr14 - 100300511 100300511 100300511 GGGTGTGGTGGCTCATGCCTGTTGTCTCAGCTACTTGGGAGGCTAAGGCAGGAGGGTCGATTGAG GGGTGTGGTGGCTCATGCCTGTTGTCTCAGCTGCTTGGGAGGCTAAGGCAGGAGGGTCGATTGAG T C SLC25A29 Ensembl:ENSG00000197119 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs186549514 Functional Loss SNV dbSNP153 33..33 33 - - - 7069 RMVar_ID_7069 Human_SNP_ID_567265723 A-to-I Human chr14 - 100300561 100300561 100300561 GCCTGGGCAGCATGGCAAGACCCATCCTGCCAAAATTACAAAAATTAGCTGGGTGTGGTGGCTCA GCCTGGGCAGCATGGCAAGACCCATCCTGCCACAATTACAAAAATTAGCTGGGTGTGGTGGCTCA T G SLC25A29 Ensembl:ENSG00000197119 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs972976056 Functional Loss SNV dbSNP153 33..33 33 - - - 7070 RMVar_ID_7070 Human_SNP_ID_567265743 A-to-I Human chr14 - 100300659 100300659 100300659 GGTTCAAAACTACACATTGGGCACAGTGGCTCATGTCTGTAATCCCAGCACTTTGGGAGGCTTGG GGTTCAAAACTACACATTGGGCACAGTGGCTCTTGTCTGTAATCCCAGCACTTTGGGAGGCTTGG T A SLC25A29 Ensembl:ENSG00000197119 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991926573 Functional Loss SNV dbSNP153 33..33 33 - - - 7071 RMVar_ID_7071 Human_SNP_ID_567265744 A-to-I Human chr14 - 100300659 100300659 100300659 GGTTCAAAACTACACATTGGGCACAGTGGCTCATGTCTGTAATCCCAGCACTTTGGGAGGCTTGG GGTTCAAAACTACACATTGGGCACAGTGGCTCGTGTCTGTAATCCCAGCACTTTGGGAGGCTTGG T C SLC25A29 Ensembl:ENSG00000197119 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991926573 Functional Loss SNV dbSNP153 33..33 33 - - - 7072 RMVar_ID_7072 Human_SNP_ID_567266038 A-to-I Human chr14 - 100301715 100301715 100301715 ACGAGGTCAGGAGATCGAGACCATCCTGGCTAACAAAGGTGAAACCCCGTCTCTACTAAATATGC ACGAGGTCAGGAGATCGAGACCATCCTGGCTAGCAAAGGTGAAACCCCGTCTCTACTAAATATGC T C SLC25A29 Ensembl:ENSG00000197119 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1339939962 Functional Loss SNV dbSNP153 33..33 33 - - - 7073 RMVar_ID_7073 Human_SNP_ID_567275674 A-to-I Human chr14 - 100335086 100335086 100335086 GGCTGAGCTGGTGCCCGAGGCAGGAAGGAGCCACTCAGGACATGTGGAGCCATCTCTCACGTGGC GGCTGAGCTGGTGCCCGAGGCAGGAAGGAGCCTCTCAGGACATGTGGAGCCATCTCTCACGTGGC T A WARS1 Ensembl:ENSG00000140105 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2234532 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92847,RMVar_hsa_circ_124164,RMVar_hsa_circ_127132,RMVar_hsa_circ_108099,RMVar_hsa_circ_169031,RMVar_hsa_circ_82436,RMVar_hsa_circ_91764,RMVar_hsa_circ_169033,RMVar_hsa_circ_169034,RMVar_hsa_circ_169032,RMVar_hsa_circ_169029,RMVar_hsa_circ_169030 7074 RMVar_ID_7074 Human_SNP_ID_567275675 A-to-I Human chr14 - 100335086 100335086 100335086 GGCTGAGCTGGTGCCCGAGGCAGGAAGGAGCCACTCAGGACATGTGGAGCCATCTCTCACGTGGC GGCTGAGCTGGTGCCCGAGGCAGGAAGGAGCCGCTCAGGACATGTGGAGCCATCTCTCACGTGGC T C WARS1 Ensembl:ENSG00000140105 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2234532 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92847,RMVar_hsa_circ_124164,RMVar_hsa_circ_127132,RMVar_hsa_circ_108099,RMVar_hsa_circ_169031,RMVar_hsa_circ_82436,RMVar_hsa_circ_91764,RMVar_hsa_circ_169033,RMVar_hsa_circ_169034,RMVar_hsa_circ_169032,RMVar_hsa_circ_169029,RMVar_hsa_circ_169030 7075 RMVar_ID_7075 Human_SNP_ID_567275789 A-to-I Human chr14 - 100335502 100335502 100335502 GTGGTGGCAGGCACCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCTG GTGGTGGCAGGCACCTGTAATCCCAGCTACTCTGGAGGCTGAGGCAGGAGAATCACTTGAACCTG T A WARS1 Ensembl:ENSG00000140105 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1427160942 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92847,RMVar_hsa_circ_124164,RMVar_hsa_circ_127132,RMVar_hsa_circ_108099,RMVar_hsa_circ_169031,RMVar_hsa_circ_82436,RMVar_hsa_circ_91764,RMVar_hsa_circ_169033,RMVar_hsa_circ_169034,RMVar_hsa_circ_169032,RMVar_hsa_circ_169029,RMVar_hsa_circ_169030 7076 RMVar_ID_7076 Human_SNP_ID_567275793 A-to-I Human chr14 - 100335526 100335526 100335526 TAAAAATACAAAAATTAGCCAGGCGTGGTGGCAGGCACCTGTAATCCCAGCTACTCAGGAGGCTG TAAAAATACAAAAATTAGCCAGGCGTGGTGGCCGGCACCTGTAATCCCAGCTACTCAGGAGGCTG T G WARS1 Ensembl:ENSG00000140105 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs963571908 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92847,RMVar_hsa_circ_124164,RMVar_hsa_circ_127132,RMVar_hsa_circ_108099,RMVar_hsa_circ_169031,RMVar_hsa_circ_82436,RMVar_hsa_circ_91764,RMVar_hsa_circ_169033,RMVar_hsa_circ_169034,RMVar_hsa_circ_169032,RMVar_hsa_circ_169029,RMVar_hsa_circ_169030 7077 RMVar_ID_7077 Human_SNP_ID_567275946 A-to-I Human chr14 - 100336081 100336081 100336081 TTAGTAGAGACAGGGTTTTACCGTCTTATTCAAGATGGTCTCGACCTCCCGACCTCGTGATCCAC TTAGTAGAGACAGGGTTTTACCGTCTTATTCAGGATGGTCTCGACCTCCCGACCTCGTGATCCAC T C WARS1 Ensembl:ENSG00000140105 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1408585173 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12267055 RMVar_hsa_circ_92847,RMVar_hsa_circ_124164,RMVar_hsa_circ_127132,RMVar_hsa_circ_108099,RMVar_hsa_circ_169031,RMVar_hsa_circ_82436,RMVar_hsa_circ_91764,RMVar_hsa_circ_169033,RMVar_hsa_circ_169034,RMVar_hsa_circ_169032,RMVar_hsa_circ_169029,RMVar_hsa_circ_169030 7078 RMVar_ID_7078 Human_SNP_ID_567276294 A-to-I Human chr14 - 100337345 100337345 100337345 AGCAGTGGGTCCCCCACTGGCTGTGCGCCCCCAACCGGCTGTGCGCCTTGGCCTTTCCCGGGTCC AGCAGTGGGTCCCCCACTGGCTGTGCGCCCCCTACCGGCTGTGCGCCTTGGCCTTTCCCGGGTCC T A WARS1 Ensembl:ENSG00000140105 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4905951 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3583,RMVar_hsa_circ_92847,RMVar_hsa_circ_127132,RMVar_hsa_circ_108099,RMVar_hsa_circ_169031,RMVar_hsa_circ_82436,RMVar_hsa_circ_91764,RMVar_hsa_circ_169033,RMVar_hsa_circ_169034,RMVar_hsa_circ_169032,RMVar_hsa_circ_169030,RMVar_hsa_circ_277427,RMVar_hsa_circ_355351,RMVar_hsa_circ_362448,RMVar_hsa_circ_53910,RMVar_hsa_circ_169035 7079 RMVar_ID_7079 Human_SNP_ID_567276295 A-to-I Human chr14 - 100337345 100337345 100337345 AGCAGTGGGTCCCCCACTGGCTGTGCGCCCCCAACCGGCTGTGCGCCTTGGCCTTTCCCGGGTCC AGCAGTGGGTCCCCCACTGGCTGTGCGCCCCCGACCGGCTGTGCGCCTTGGCCTTTCCCGGGTCC T C WARS1 Ensembl:ENSG00000140105 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4905951 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3583,RMVar_hsa_circ_92847,RMVar_hsa_circ_127132,RMVar_hsa_circ_108099,RMVar_hsa_circ_169031,RMVar_hsa_circ_82436,RMVar_hsa_circ_91764,RMVar_hsa_circ_169033,RMVar_hsa_circ_169034,RMVar_hsa_circ_169032,RMVar_hsa_circ_169030,RMVar_hsa_circ_277427,RMVar_hsa_circ_355351,RMVar_hsa_circ_362448,RMVar_hsa_circ_53910,RMVar_hsa_circ_169035 7080 RMVar_ID_7080 Human_SNP_ID_567276356 A-to-I Human chr14 - 100337616 100337616 100337616 GACCTCCTGGCCTCAATCGATCCTCCCCCCTCAGCCTCCCAAAATGCTGAGATTACTGGCACAAG GACCTCCTGGCCTCAATCGATCCTCCCCCCTCCGCCTCCCAAAATGCTGAGATTACTGGCACAAG T G WARS1 Ensembl:ENSG00000140105 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1194495547 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3583,RMVar_hsa_circ_92847,RMVar_hsa_circ_127132,RMVar_hsa_circ_108099,RMVar_hsa_circ_169031,RMVar_hsa_circ_82436,RMVar_hsa_circ_91764,RMVar_hsa_circ_169033,RMVar_hsa_circ_169034,RMVar_hsa_circ_169032,RMVar_hsa_circ_169030,RMVar_hsa_circ_277427,RMVar_hsa_circ_355351,RMVar_hsa_circ_362448,RMVar_hsa_circ_53910,RMVar_hsa_circ_169035 7081 RMVar_ID_7081 Human_SNP_ID_567276629 A-to-I Human chr14 - 100338685 100338685 100338685 TCATGCCTGCAGTTCCAGCACTTTGGGAGGCCAAGGCAGGCGAATCACCTGAGGTTGGGAGTTCA TCATGCCTGCAGTTCCAGCACTTTGGGAGGCCGAGGCAGGCGAATCACCTGAGGTTGGGAGTTCA T C WARS1 Ensembl:ENSG00000140105 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1566834743 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3583,RMVar_hsa_circ_92847,RMVar_hsa_circ_127132,RMVar_hsa_circ_108099,RMVar_hsa_circ_169031,RMVar_hsa_circ_82436,RMVar_hsa_circ_91764,RMVar_hsa_circ_169033,RMVar_hsa_circ_169034,RMVar_hsa_circ_169032,RMVar_hsa_circ_169030,RMVar_hsa_circ_277427,RMVar_hsa_circ_355351,RMVar_hsa_circ_362448,RMVar_hsa_circ_53910,RMVar_hsa_circ_169035 7082 RMVar_ID_7082 Human_SNP_ID_567276674 A-to-I Human chr14 - 100338944 100338944 100338944 ATGACACCACGCCCAGCTAATTTTGTAGTTTCAGTAGAGACGGGGTTTCTTCATGTTGGTCAGGC ATGACACCACGCCCAGCTAATTTTGTAGTTTCGGTAGAGACGGGGTTTCTTCATGTTGGTCAGGC T C WARS1 Ensembl:ENSG00000140105 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs190061498 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3583,RMVar_hsa_circ_92847,RMVar_hsa_circ_127132,RMVar_hsa_circ_108099,RMVar_hsa_circ_169031,RMVar_hsa_circ_82436,RMVar_hsa_circ_91764,RMVar_hsa_circ_169033,RMVar_hsa_circ_169034,RMVar_hsa_circ_169032,RMVar_hsa_circ_169030,RMVar_hsa_circ_277427,RMVar_hsa_circ_355351,RMVar_hsa_circ_362448,RMVar_hsa_circ_53910,RMVar_hsa_circ_169035 7083 RMVar_ID_7083 Human_SNP_ID_567276689 A-to-I Human chr14 - 100339005 100339005 100339005 GCCTCCCGGGTTCAAGCGATTCTCCTGCCTCAACCTCCCAAATAGCTGGGATTACAGGCACATGA GCCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAATAGCTGGGATTACAGGCACATGA T C WARS1 Ensembl:ENSG00000140105 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs970376437 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3583,RMVar_hsa_circ_92847,RMVar_hsa_circ_127132,RMVar_hsa_circ_108099,RMVar_hsa_circ_169031,RMVar_hsa_circ_82436,RMVar_hsa_circ_91764,RMVar_hsa_circ_169033,RMVar_hsa_circ_169034,RMVar_hsa_circ_169032,RMVar_hsa_circ_169030,RMVar_hsa_circ_277427,RMVar_hsa_circ_355351,RMVar_hsa_circ_362448,RMVar_hsa_circ_53910,RMVar_hsa_circ_169035 7084 RMVar_ID_7084 Human_SNP_ID_567276895 A-to-I Human chr14 - 100339402 100339402 100339402 GTATTTTGGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGGTCTTGATCTCCTGACCTCGTAA GTATTTTGGTAGAGACGGGGTTTCACCGTGTTGGCCAGGATGGTCTTGATCTCCTGACCTCGTAA T C WARS1 Ensembl:ENSG00000140105 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs555210102 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3583,RMVar_hsa_circ_92847,RMVar_hsa_circ_127132,RMVar_hsa_circ_108099,RMVar_hsa_circ_169031,RMVar_hsa_circ_82436,RMVar_hsa_circ_91764,RMVar_hsa_circ_169033,RMVar_hsa_circ_169034,RMVar_hsa_circ_169032,RMVar_hsa_circ_169030,RMVar_hsa_circ_277427,RMVar_hsa_circ_355351,RMVar_hsa_circ_362448,RMVar_hsa_circ_53910,RMVar_hsa_circ_169035 7085 RMVar_ID_7085 Human_SNP_ID_567276928 A-to-I Human chr14 - 100339450 100339450 100339450 GAGTAGCTGGGCCTACAGGCGCCCACCACCACACCCAGCTAATTTTTTGTATTTTGGTAGAGACG GAGTAGCTGGGCCTACAGGCGCCCACCACCACTCCCAGCTAATTTTTTGTATTTTGGTAGAGACG T A WARS1 Ensembl:ENSG00000140105 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11620717 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3583,RMVar_hsa_circ_92847,RMVar_hsa_circ_127132,RMVar_hsa_circ_108099,RMVar_hsa_circ_169031,RMVar_hsa_circ_82436,RMVar_hsa_circ_91764,RMVar_hsa_circ_169033,RMVar_hsa_circ_169034,RMVar_hsa_circ_169032,RMVar_hsa_circ_169030,RMVar_hsa_circ_277427,RMVar_hsa_circ_355351,RMVar_hsa_circ_362448,RMVar_hsa_circ_53910,RMVar_hsa_circ_169035 7086 RMVar_ID_7086 Human_SNP_ID_567276929 A-to-I Human chr14 - 100339450 100339450 100339450 GAGTAGCTGGGCCTACAGGCGCCCACCACCACACCCAGCTAATTTTTTGTATTTTGGTAGAGACG GAGTAGCTGGGCCTACAGGCGCCCACCACCACGCCCAGCTAATTTTTTGTATTTTGGTAGAGACG T C WARS1 Ensembl:ENSG00000140105 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11620717 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3583,RMVar_hsa_circ_92847,RMVar_hsa_circ_127132,RMVar_hsa_circ_108099,RMVar_hsa_circ_169031,RMVar_hsa_circ_82436,RMVar_hsa_circ_91764,RMVar_hsa_circ_169033,RMVar_hsa_circ_169034,RMVar_hsa_circ_169032,RMVar_hsa_circ_169030,RMVar_hsa_circ_277427,RMVar_hsa_circ_355351,RMVar_hsa_circ_362448,RMVar_hsa_circ_53910,RMVar_hsa_circ_169035 7087 RMVar_ID_7087 Human_SNP_ID_567277423 A-to-I Human chr14 - 100341191 100341191 100341191 TTGTTTATGGCCAGGTGCGATAGCTCACACCTATAATTCCAGCACTTTGAGAGGCCGAGGCAGGT TTGTTTATGGCCAGGTGCGATAGCTCACACCTGTAATTCCAGCACTTTGAGAGGCCGAGGCAGGT T C WARS1 Ensembl:ENSG00000140105 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1177969120 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3583,RMVar_hsa_circ_92847,RMVar_hsa_circ_127132,RMVar_hsa_circ_108099,RMVar_hsa_circ_169031,RMVar_hsa_circ_82436,RMVar_hsa_circ_91764,RMVar_hsa_circ_169033,RMVar_hsa_circ_169034,RMVar_hsa_circ_169032,RMVar_hsa_circ_169030,RMVar_hsa_circ_277427,RMVar_hsa_circ_355351,RMVar_hsa_circ_362448,RMVar_hsa_circ_53910,RMVar_hsa_circ_169035 7088 RMVar_ID_7088 Human_SNP_ID_567279968 A-to-I Human chr14 - 100350348 100350348 100350348 TTGCTCTGTCGCCCAAACTGGAGAGCAGTGGCATGATCTCGGCTTACTGCAATATCTGCCTCCTG TTGCTCTGTCGCCCAAACTGGAGAGCAGTGGCTTGATCTCGGCTTACTGCAATATCTGCCTCCTG T A WARS1 Ensembl:ENSG00000140105 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1252260255 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3583,RMVar_hsa_circ_92847,RMVar_hsa_circ_108099,RMVar_hsa_circ_169031,RMVar_hsa_circ_82436,RMVar_hsa_circ_91764,RMVar_hsa_circ_169033,RMVar_hsa_circ_169034,RMVar_hsa_circ_169032,RMVar_hsa_circ_362448,RMVar_hsa_circ_53910,RMVar_hsa_circ_22120,RMVar_hsa_circ_315426,RMVar_hsa_circ_310387,RMVar_hsa_circ_169036,RMVar_hsa_circ_2855,RMVar_hsa_circ_266798 7089 RMVar_ID_7089 Human_SNP_ID_567279969 A-to-I Human chr14 - 100350348 100350348 100350348 TTGCTCTGTCGCCCAAACTGGAGAGCAGTGGCATGATCTCGGCTTACTGCAATATCTGCCTCCTG TTGCTCTGTCGCCCAAACTGGAGAGCAGTGGCGTGATCTCGGCTTACTGCAATATCTGCCTCCTG T C WARS1 Ensembl:ENSG00000140105 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1252260255 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3583,RMVar_hsa_circ_92847,RMVar_hsa_circ_108099,RMVar_hsa_circ_169031,RMVar_hsa_circ_82436,RMVar_hsa_circ_91764,RMVar_hsa_circ_169033,RMVar_hsa_circ_169034,RMVar_hsa_circ_169032,RMVar_hsa_circ_362448,RMVar_hsa_circ_53910,RMVar_hsa_circ_22120,RMVar_hsa_circ_315426,RMVar_hsa_circ_310387,RMVar_hsa_circ_169036,RMVar_hsa_circ_2855,RMVar_hsa_circ_266798 7090 RMVar_ID_7090 Human_SNP_ID_567283049 A-to-I Human chr14 - 100363581 100363581 100363581 GCAATCCTCTGACTTCAGCCTCCCGATGAGCTAGGAACACAGGTGTGTGCCACCACACCTGGCTA GCAATCCTCTGACTTCAGCCTCCCGATGAGCTGGGAACACAGGTGTGTGCCACCACACCTGGCTA T C WARS1 Ensembl:ENSG00000140105 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1304898142 Functional Loss SNV dbSNP153 33..33 33 - - - 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 7091 RMVar_ID_7091 Human_SNP_ID_567283934 A-to-I Human chr14 + 100366778 100366778 100366778 CTAAGGGATCCGTGGGGCCACAATGAAGCTTGAAGATACATGGGTGGCTTTGCAAAGAGTGTTTC CTAAGGGATCCGTGGGGCCACAATGAAGCTTGGAGATACATGGGTGGCTTTGCAAAGAGTGTTTC A G AL157871.3 Ensembl:ENSG00000258581 Pseudogene exon GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs878989366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1883251 7092 RMVar_ID_7092 Human_SNP_ID_567284701 A-to-I Human chr14 - 100369837 100369837 100369837 CAACATGGTGAAACCCTCCCTCTACTAAAAATACAAAAATTCGCTGGGCATGGTGGCAGGCAGCC CAACATGGTGAAACCCTCCCTCTACTAAAAATGCAAAAATTCGCTGGGCATGGTGGCAGGCAGCC T C WARS1 Ensembl:ENSG00000140105 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1276248969 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17844515 RMVar_hsa_circ_82436,RMVar_hsa_circ_169034,RMVar_hsa_circ_53910,RMVar_hsa_circ_95133,RMVar_hsa_circ_121644,RMVar_hsa_circ_169046,RMVar_hsa_circ_169047 7093 RMVar_ID_7093 Human_SNP_ID_567284703 A-to-I Human chr14 - 100369839 100369839 100369839 GCCAACATGGTGAAACCCTCCCTCTACTAAAAATACAAAAATTCGCTGGGCATGGTGGCAGGCAG GCCAACATGGTGAAACCCTCCCTCTACTAAAACTACAAAAATTCGCTGGGCATGGTGGCAGGCAG T G WARS1 Ensembl:ENSG00000140105 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1369767517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17844515 RMVar_hsa_circ_82436,RMVar_hsa_circ_169034,RMVar_hsa_circ_53910,RMVar_hsa_circ_95133,RMVar_hsa_circ_121644,RMVar_hsa_circ_169046,RMVar_hsa_circ_169047 7094 RMVar_ID_7094 Human_SNP_ID_567406119 A-to-I Human chr14 + 100846418 100846418 100846418 CGCGAGCCCCAGAAGGATCTGGGAGTAAACTTAACATTCACTGTGTCTCTGCTCTGCATCCGCCA CGCGAGCCCCAGAAGGATCTGGGAGTAAACTTGACATTCACTGTGTCTCTGCTCTGCATCCGCCA A G MEG3,AL117190.1 Ensembl:ENSG00000214548,Ensembl:ENSG00000258399 lincRNA,lincRNA intron,intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1039190136 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9038843,Human_RBP_ID_23611025 7095 RMVar_ID_7095 Human_SNP_ID_567407279 A-to-I Human chr14 + 100851441 100851440 100851441 CACATCCAGGGGTTGGTGCAGGGAAAGGCCAGAAGGTGGCCAGGCGCACCTGAGAAGGGGGACCC CACATCCAGGGGTTGGTGCAGGGAAAGGCCAG_AGGTGGCCAGGCGCACCTGAGAAGGGGGACCC GA G MEG3,AL117190.1 Ensembl:ENSG00000214548,Ensembl:ENSG00000258399 lincRNA,lincRNA intron,intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1353437494 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_9038910 7096 RMVar_ID_7096 Human_SNP_ID_567407290 A-to-I Human chr14 + 100851476 100851476 100851476 GTGGCCAGGCGCACCTGAGAAGGGGGACCCAGAAGCCCCGGGACCCAGGAGCCCTGGGCAAGCCA GTGGCCAGGCGCACCTGAGAAGGGGGACCCAGCAGCCCCGGGACCCAGGAGCCCTGGGCAAGCCA A C MEG3,AL117190.1 Ensembl:ENSG00000214548,Ensembl:ENSG00000258399 lincRNA,lincRNA intron,intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs893379458 Functional Loss SNV dbSNP153 33..33 33 - - - 7097 RMVar_ID_7097 Human_SNP_ID_567408566 A-to-I Human chr14 + 100856455 100856455 100856455 AGTCACTGTGAGAGCTGGAGTTGAGTCTGCCTACGGGGGAGGACTGCGGCACCTACCTCGCAGGG AGTCACTGTGAGAGCTGGAGTTGAGTCTGCCTTCGGGGGAGGACTGCGGCACCTACCTCGCAGGG A T MEG3,AL117190.1 Ensembl:ENSG00000214548,Ensembl:ENSG00000258399 lincRNA,lincRNA intron,intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1005871346 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9038980,Human_RBP_ID_23611112 7098 RMVar_ID_7098 Human_SNP_ID_567436649 A-to-I Human chr14 + 100960067 100960067 100960067 ATGGTGGCGCATGTCTTTAATTCCAGCTACTCAGGAGGCTGAGGCAGGAGAAACGCTTGAACCCG ATGGTGGCGCATGTCTTTAATTCCAGCTACTCCGGAGGCTGAGGCAGGAGAAACGCTTGAACCCG A C MEG8 Ensembl:ENSG00000225746 lincRNA exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1351304286 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1554382,Human_Splice_Rec_1554608 RMVar_hsa_circ_683,RMVar_hsa_circ_65404,RMVar_hsa_circ_59785,RMVar_hsa_circ_11975,RMVar_hsa_circ_14809,RMVar_hsa_circ_16180,RMVar_hsa_circ_59653,RMVar_hsa_circ_57518,RMVar_hsa_circ_361257,RMVar_hsa_circ_357937,RMVar_hsa_circ_356090,RMVar_hsa_circ_347619,RMVar_hsa_circ_53803,RMVar_hsa_circ_69506,RMVar_hsa_circ_169067,RMVar_hsa_circ_169075,RMVar_hsa_circ_346589,RMVar_hsa_circ_347480,RMVar_hsa_circ_351799,RMVar_hsa_circ_338316,RMVar_hsa_circ_303280,RMVar_hsa_circ_302748,RMVar_hsa_circ_271892,RMVar_hsa_circ_300317,RMVar_hsa_circ_58561,RMVar_hsa_circ_63007,RMVar_hsa_circ_56479,RMVar_hsa_circ_169078,RMVar_hsa_circ_6042,RMVar_hsa_circ_37401,RMVar_hsa_circ_3977,RMVar_hsa_circ_345391,RMVar_hsa_circ_357346,RMVar_hsa_circ_169076,RMVar_hsa_circ_169077,RMVar_hsa_circ_366433,RMVar_hsa_circ_368364,RMVar_hsa_circ_360818,RMVar_hsa_circ_354046,RMVar_hsa_circ_316235,RMVar_hsa_circ_314846,RMVar_hsa_circ_294144,RMVar_hsa_circ_290817,RMVar_hsa_circ_700,RMVar_hsa_circ_65539,RMVar_hsa_circ_284444,RMVar_hsa_circ_57893,RMVar_hsa_circ_59194,RMVar_hsa_circ_169086,RMVar_hsa_circ_169088,RMVar_hsa_circ_169089,RMVar_hsa_circ_169087,RMVar_hsa_circ_169084,RMVar_hsa_circ_169085,RMVar_hsa_circ_319895,RMVar_hsa_circ_318204,RMVar_hsa_circ_63908,RMVar_hsa_circ_50249,RMVar_hsa_circ_169097,RMVar_hsa_circ_367012,RMVar_hsa_circ_343334,RMVar_hsa_circ_329039,RMVar_hsa_circ_18655,RMVar_hsa_circ_12089,RMVar_hsa_circ_15927,RMVar_hsa_circ_347185,RMVar_hsa_circ_356082,RMVar_hsa_circ_169098,RMVar_hsa_circ_367618,RMVar_hsa_circ_348481,RMVar_hsa_circ_333722,RMVar_hsa_circ_57842,RMVar_hsa_circ_24205,RMVar_hsa_circ_353309,RMVar_hsa_circ_331642,RMVar_hsa_circ_57946,RMVar_hsa_circ_299603,RMVar_hsa_circ_28603,RMVar_hsa_circ_169103,RMVar_hsa_circ_6587,RMVar_hsa_circ_19513,RMVar_hsa_circ_169105,RMVar_hsa_circ_169104,RMVar_hsa_circ_66409,RMVar_hsa_circ_32342,RMVar_hsa_circ_53200,RMVar_hsa_circ_27321,RMVar_hsa_circ_47489,RMVar_hsa_circ_66488,RMVar_hsa_circ_40766,RMVar_hsa_circ_347102,RMVar_hsa_circ_169108,RMVar_hsa_circ_351062,RMVar_hsa_circ_357450,RMVar_hsa_circ_329063,RMVar_hsa_circ_338046,RMVar_hsa_circ_311779,RMVar_hsa_circ_46107,RMVar_hsa_circ_49507,RMVar_hsa_circ_51180,RMVar_hsa_circ_48168,RMVar_hsa_circ_42568,RMVar_hsa_circ_65915,RMVar_hsa_circ_169110,RMVar_hsa_circ_44308,RMVar_hsa_circ_13301,RMVar_hsa_circ_24412,RMVar_hsa_circ_61595,RMVar_hsa_circ_69786,RMVar_hsa_circ_335898,RMVar_hsa_circ_364781,RMVar_hsa_circ_309577,RMVar_hsa_circ_62878,RMVar_hsa_circ_45636,RMVar_hsa_circ_8590,RMVar_hsa_circ_47283,RMVar_hsa_circ_73487 7099 RMVar_ID_7099 Human_SNP_ID_567660139 A-to-I Human chr14 + 101818527 101818527 101818527 CGTGGTGGCGGGTGCCTGTAATCCCAGCTACTAGGGAGGTTGAGGCAGGAGAATCACTTAAACCT CGTGGTGGCGGGTGCCTGTAATCCCAGCTACTGGGGAGGTTGAGGCAGGAGAATCACTTAAACCT A G PPP2R5C Ensembl:ENSG00000078304 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1251529648 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_119720 RMVar_hsa_circ_169138,RMVar_hsa_circ_89959,RMVar_hsa_circ_169139,RMVar_hsa_circ_118240 7100 RMVar_ID_7100 Human_SNP_ID_567671218 A-to-I Human chr14 + 101863806 101863806 101863806 TGTAATCCCAGCTACTTGGAAGACTGAGGCAGAAGAATCACTTGAACCCGGGAGTGGGAGGTTGC TGTAATCCCAGCTACTTGGAAGACTGAGGCAGCAGAATCACTTGAACCCGGGAGTGGGAGGTTGC A C PPP2R5C Ensembl:ENSG00000078304 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1333903175 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8274,RMVar_hsa_circ_17037,RMVar_hsa_circ_169138,RMVar_hsa_circ_89959,RMVar_hsa_circ_169139,RMVar_hsa_circ_118240,RMVar_hsa_circ_314746,RMVar_hsa_circ_268038,RMVar_hsa_circ_85649,RMVar_hsa_circ_169141,RMVar_hsa_circ_169140 7101 RMVar_ID_7101 Human_SNP_ID_567672151 A-to-I Human chr14 + 101867601 101867601 101867601 GGAGCTCGAGACCAGCCTGACCAGTATGGTGTAACCTCATCTCTACTAAAAATATGAAAATTAGC GGAGCTCGAGACCAGCCTGACCAGTATGGTGTGACCTCATCTCTACTAAAAATATGAAAATTAGC A G PPP2R5C Ensembl:ENSG00000078304 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924085328 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8274,RMVar_hsa_circ_17037,RMVar_hsa_circ_169138,RMVar_hsa_circ_89959,RMVar_hsa_circ_169139,RMVar_hsa_circ_118240,RMVar_hsa_circ_314746,RMVar_hsa_circ_268038,RMVar_hsa_circ_85649,RMVar_hsa_circ_169141,RMVar_hsa_circ_169140 7102 RMVar_ID_7102 Human_SNP_ID_567672155 A-to-I Human chr14 + 101867613 101867613 101867613 CAGCCTGACCAGTATGGTGTAACCTCATCTCTACTAAAAATATGAAAATTAGCCAGGCATGGTGG CAGCCTGACCAGTATGGTGTAACCTCATCTCTGCTAAAAATATGAAAATTAGCCAGGCATGGTGG A G PPP2R5C Ensembl:ENSG00000078304 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1448962124 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8274,RMVar_hsa_circ_17037,RMVar_hsa_circ_169138,RMVar_hsa_circ_89959,RMVar_hsa_circ_169139,RMVar_hsa_circ_118240,RMVar_hsa_circ_314746,RMVar_hsa_circ_268038,RMVar_hsa_circ_85649,RMVar_hsa_circ_169141,RMVar_hsa_circ_169140 7103 RMVar_ID_7103 Human_SNP_ID_567677107 A-to-I Human chr14 + 101887301 101887301 101887301 CTTGCTGCATAACCAGCCATGGGTCATGCTCTATCCTCACCCTGGCCCTGCAGCAAGGCTGTGCA CTTGCTGCATAACCAGCCATGGGTCATGCTCTGTCCTCACCCTGGCCCTGCAGCAAGGCTGTGCA A G PPP2R5C Ensembl:ENSG00000078304 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1007451966 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19912646 RMVar_hsa_circ_8274,RMVar_hsa_circ_17037,RMVar_hsa_circ_169138,RMVar_hsa_circ_89959,RMVar_hsa_circ_268038,RMVar_hsa_circ_169142,RMVar_hsa_circ_272381,RMVar_hsa_circ_169141,RMVar_hsa_circ_302301,RMVar_hsa_circ_327619,RMVar_hsa_circ_371565,RMVar_hsa_circ_310225,RMVar_hsa_circ_287401,RMVar_hsa_circ_122123,RMVar_hsa_circ_169144,RMVar_hsa_circ_169145,RMVar_hsa_circ_169143,RMVar_hsa_circ_169146,RMVar_hsa_circ_304354,RMVar_hsa_circ_351212,RMVar_hsa_circ_26051,RMVar_hsa_circ_322908,RMVar_hsa_circ_372974,RMVar_hsa_circ_51153 7104 RMVar_ID_7104 Human_SNP_ID_567697840 A-to-I Human chr14 + 101967692 101967692 101967692 CAAGACCCTATCTCTACAGAAAATTAAAAAATAAGCCAGGCATGGTGGTGTATGCCAGTAGTTCC CAAGACCCTATCTCTACAGAAAATTAAAAAATTAGCCAGGCATGGTGGTGTATGCCAGTAGTTCC A T DYNC1H1 Ensembl:ENSG00000197102 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1368710879 Functional Loss SNV dbSNP153 33..33 33 - - - 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 7105 RMVar_ID_7105 Human_SNP_ID_567705232 A-to-I Human chr14 + 101996875 101996875 101996875 AAACTCCTGGACTCAAGTAATCCACCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCAAGAA AAACTCCTGGACTCAAGTAATCCACCTGCCTCCGCCTCCCAAAGTGCTGGGATTACAGGCAAGAA A C DYNC1H1 Ensembl:ENSG00000197102 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1188406790 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_100522,RMVar_hsa_circ_103974,RMVar_hsa_circ_169166,RMVar_hsa_circ_169167,RMVar_hsa_circ_169164,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_82703,RMVar_hsa_circ_169190,RMVar_hsa_circ_88091,RMVar_hsa_circ_169189,RMVar_hsa_circ_105453,RMVar_hsa_circ_352907,RMVar_hsa_circ_169193,RMVar_hsa_circ_336104,RMVar_hsa_circ_277110,RMVar_hsa_circ_90357,RMVar_hsa_circ_47390,RMVar_hsa_circ_112304,RMVar_hsa_circ_169196,RMVar_hsa_circ_169197,RMVar_hsa_circ_169198,RMVar_hsa_circ_169195,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_268155,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_169214,RMVar_hsa_circ_62534,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 7106 RMVar_ID_7106 Human_SNP_ID_567706988 A-to-I Human chr14 + 102003282 102003280 102003282 TATCTCTGGCAGTTTTCTTTTTTTTTTTTTTGAGATGGAGTCTTGCTCTGTCGCCCAGGCTGGAG TATCTCTGGCAGTTTTCTTTTTTTTTTTTTT__GATGGAGTCTTGCTCTGTCGCCCAGGCTGGAG TGA T DYNC1H1 Ensembl:ENSG00000197102 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1293116996 Functional Loss DEL dbSNP153 32..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_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_62534,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_2837,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_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_312591,RMVar_hsa_circ_169244,RMVar_hsa_circ_169245,RMVar_hsa_circ_169243 7107 RMVar_ID_7107 Human_SNP_ID_567706990 A-to-I Human chr14 + 102003282 102003282 102003282 TATCTCTGGCAGTTTTCTTTTTTTTTTTTTTGAGATGGAGTCTTGCTCTGTCGCCCAGGCTGGAG TATCTCTGGCAGTTTTCTTTTTTTTTTTTTTGTGATGGAGTCTTGCTCTGTCGCCCAGGCTGGAG A T DYNC1H1 Ensembl:ENSG00000197102 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1252644066 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_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_62534,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_2837,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_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_312591,RMVar_hsa_circ_169244,RMVar_hsa_circ_169245,RMVar_hsa_circ_169243 7108 RMVar_ID_7108 Human_SNP_ID_567707064 A-to-I Human chr14 + 102003529 102003529 102003529 GGTGAGCCGCTCACCTAAGTCACCTAAGTGCTAGGATTACAGGCATGAGCCACTGCACCCAGCCT GGTGAGCCGCTCACCTAAGTCACCTAAGTGCTGGGATTACAGGCATGAGCCACTGCACCCAGCCT A G DYNC1H1 Ensembl:ENSG00000197102 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1440436740 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17562751 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_62534,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_2837,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_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_312591,RMVar_hsa_circ_169244,RMVar_hsa_circ_169245,RMVar_hsa_circ_169243 7109 RMVar_ID_7109 Human_SNP_ID_567711834 A-to-I Human chr14 + 102021997 102021997 102021997 ATCTCTACTAAAAATACAAAAATTAGCTGGGCATGGTAGCATATGCCTGTAATCCCAGCTACTGA ATCTCTACTAAAAATACAAAAATTAGCTGGGCGTGGTAGCATATGCCTGTAATCCCAGCTACTGA A G DYNC1H1 Ensembl:ENSG00000197102 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs753195698 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_169285,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_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_169299,RMVar_hsa_circ_169297,RMVar_hsa_circ_278395,RMVar_hsa_circ_169302,RMVar_hsa_circ_169303 7110 RMVar_ID_7110 Human_SNP_ID_567713011 A-to-I Human chr14 + 102026319 102026319 102026319 GGCATTTTTATAGTAGAGTGTTTTTTTCCTCCATGATCATGGTATGTCTCTTCATGTATTGAGGT GGCATTTTTATAGTAGAGTGTTTTTTTCCTCCGTGATCATGGTATGTCTCTTCATGTATTGAGGT A G DYNC1H1 Ensembl:ENSG00000197102 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4900530 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_418,GWAS_ID_419,GWAS_ID_420,GWAS_ID_421,GWAS_ID_422,GWAS_ID_423,GWAS_ID_424,GWAS_ID_425,GWAS_ID_426,GWAS_ID_427,GWAS_ID_428,GWAS_ID_429,GWAS_ID_430,GWAS_ID_431 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_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_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_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_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_169275,RMVar_hsa_circ_82380,RMVar_hsa_circ_88408,RMVar_hsa_circ_169279,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_169284,RMVar_hsa_circ_169282,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_62402,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,RMVar_hsa_circ_312872,RMVar_hsa_circ_85017,RMVar_hsa_circ_127490,RMVar_hsa_circ_87538,RMVar_hsa_circ_169298,RMVar_hsa_circ_169299,RMVar_hsa_circ_169297,RMVar_hsa_circ_169303 7111 RMVar_ID_7111 Human_SNP_ID_567713012 A-to-I Human chr14 + 102026319 102026319 102026319 GGCATTTTTATAGTAGAGTGTTTTTTTCCTCCATGATCATGGTATGTCTCTTCATGTATTGAGGT GGCATTTTTATAGTAGAGTGTTTTTTTCCTCCTTGATCATGGTATGTCTCTTCATGTATTGAGGT A T DYNC1H1 Ensembl:ENSG00000197102 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4900530 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_418,GWAS_ID_419,GWAS_ID_420,GWAS_ID_421,GWAS_ID_422,GWAS_ID_423,GWAS_ID_424,GWAS_ID_425,GWAS_ID_426,GWAS_ID_427,GWAS_ID_428,GWAS_ID_429,GWAS_ID_430,GWAS_ID_431 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_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_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_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_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_169275,RMVar_hsa_circ_82380,RMVar_hsa_circ_88408,RMVar_hsa_circ_169279,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_169284,RMVar_hsa_circ_169282,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_62402,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,RMVar_hsa_circ_312872,RMVar_hsa_circ_85017,RMVar_hsa_circ_127490,RMVar_hsa_circ_87538,RMVar_hsa_circ_169298,RMVar_hsa_circ_169299,RMVar_hsa_circ_169297,RMVar_hsa_circ_169303 7112 RMVar_ID_7112 Human_SNP_ID_567714330 A-to-I Human chr14 + 102031803 102031803 102031803 ATGGAGAAACCCCGTCTCTACTAAAAATAGGAAATTAGCTGGGCGTGGTGGTGCATACCTGTAAT ATGGAGAAACCCCGTCTCTACTAAAAATAGGAGATTAGCTGGGCGTGGTGGTGCATACCTGTAAT A G DYNC1H1 Ensembl:ENSG00000197102 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs934444870 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_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_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_112304,RMVar_hsa_circ_169197,RMVar_hsa_circ_169198,RMVar_hsa_circ_118005,RMVar_hsa_circ_169200,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_100507,RMVar_hsa_circ_114823,RMVar_hsa_circ_169218,RMVar_hsa_circ_169219,RMVar_hsa_circ_169217,RMVar_hsa_circ_124093,RMVar_hsa_circ_92772,RMVar_hsa_circ_28807,RMVar_hsa_circ_113343,RMVar_hsa_circ_169220,RMVar_hsa_circ_169222,RMVar_hsa_circ_169221,RMVar_hsa_circ_105884,RMVar_hsa_circ_77475,RMVar_hsa_circ_114068,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_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_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_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_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_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_169275,RMVar_hsa_circ_96466,RMVar_hsa_circ_82380,RMVar_hsa_circ_88408,RMVar_hsa_circ_169279,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_169284,RMVar_hsa_circ_169282,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_127573,RMVar_hsa_circ_169295,RMVar_hsa_circ_169296,RMVar_hsa_circ_312872,RMVar_hsa_circ_85017,RMVar_hsa_circ_127490,RMVar_hsa_circ_87538,RMVar_hsa_circ_169298,RMVar_hsa_circ_169299,RMVar_hsa_circ_169297,RMVar_hsa_circ_102267,RMVar_hsa_circ_169303,RMVar_hsa_circ_127230,RMVar_hsa_circ_99306,RMVar_hsa_circ_169304,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_77415,RMVar_hsa_circ_30290,RMVar_hsa_circ_97484,RMVar_hsa_circ_169309,RMVar_hsa_circ_169311,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_94509,RMVar_hsa_circ_169317,RMVar_hsa_circ_169318,RMVar_hsa_circ_121359,RMVar_hsa_circ_169315,RMVar_hsa_circ_169319,RMVar_hsa_circ_93345,RMVar_hsa_circ_115331,RMVar_hsa_circ_169322,RMVar_hsa_circ_98214,RMVar_hsa_circ_169321,RMVar_hsa_circ_169323 7113 RMVar_ID_7113 Human_SNP_ID_567718094 A-to-I Human chr14 + 102045490 102045490 102045490 AAAACTAGCCAGGTGTGGTGGTGGGTGCCTGTAATCCCAGCTACTCTGGAGGCTGAGGCAGGAGA AAAACTAGCCAGGTGTGGTGGTGGGTGCCTGTCATCCCAGCTACTCTGGAGGCTGAGGCAGGAGA A C DYNC1H1 Ensembl:ENSG00000197102 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs970147750 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90357,RMVar_hsa_circ_169198,RMVar_hsa_circ_99123,RMVar_hsa_circ_169207,RMVar_hsa_circ_98599,RMVar_hsa_circ_169241,RMVar_hsa_circ_125165,RMVar_hsa_circ_169258,RMVar_hsa_circ_88408,RMVar_hsa_circ_169280,RMVar_hsa_circ_87538,RMVar_hsa_circ_169303,RMVar_hsa_circ_110513,RMVar_hsa_circ_169309,RMVar_hsa_circ_108051,RMVar_hsa_circ_169330,RMVar_hsa_circ_99163,RMVar_hsa_circ_169344,RMVar_hsa_circ_102150,RMVar_hsa_circ_112281,RMVar_hsa_circ_169346,RMVar_hsa_circ_169347,RMVar_hsa_circ_82211,RMVar_hsa_circ_169360,RMVar_hsa_circ_50150 7114 RMVar_ID_7114 Human_SNP_ID_567719806 A-to-I Human chr14 + 102050069 102050069 102050069 CACCTCAGCCTGGGTTTTGGCTTCCGCCTCACAGGTTTGAAACTTCAAGGGGCCACGTGCAACAA CACCTCAGCCTGGGTTTTGGCTTCCGCCTCACGGGTTTGAAACTTCAAGGGGCCACGTGCAACAA A G DYNC1H1 Ensembl:ENSG00000197102 Protein coding intron GSE100210;GSE105773;GSE105773 HepG2 cell line;Glioblastoma cells,U87MG;Glioblastoma cells,U87MG - 29129909,29724793,29724793 RNA-Seq:(High) rs879199744 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_40308 RMVar_hsa_circ_90357,RMVar_hsa_circ_169198,RMVar_hsa_circ_98599,RMVar_hsa_circ_169241,RMVar_hsa_circ_125165,RMVar_hsa_circ_169258,RMVar_hsa_circ_88408,RMVar_hsa_circ_169280,RMVar_hsa_circ_87538,RMVar_hsa_circ_169303,RMVar_hsa_circ_110513,RMVar_hsa_circ_169309,RMVar_hsa_circ_108051,RMVar_hsa_circ_169330,RMVar_hsa_circ_99163,RMVar_hsa_circ_169344,RMVar_hsa_circ_82211,RMVar_hsa_circ_169360,RMVar_hsa_circ_36490,RMVar_hsa_circ_120761,RMVar_hsa_circ_169366,RMVar_hsa_circ_347306 7115 RMVar_ID_7115 Human_SNP_ID_567720354 A-to-I Human chr14 + 102051878 102051878 102051878 GCCCAGCTAATTACTATATTTTTAGTAGAGACAGGGCTTCACCGTGTTGGCCAGGCTGGTCTCAA GCCCAGCTAATTACTATATTTTTAGTAGAGACGGGGCTTCACCGTGTTGGCCAGGCTGGTCTCAA A G DYNC1H1 Ensembl:ENSG00000197102 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1011373314 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12270647 7116 RMVar_ID_7116 Human_SNP_ID_567720465 A-to-I Human chr14 + 102052322 102052321 102052322 TGTCGGCTAATTTTTGTATCTTTTGTAGAGACAAGGTTTCACCATGTTGCTCGGGCTGGTCTCGA TGTCGGCTAATTTTTGTATCTTTTGTAGAGAC_AGGTTTCACCATGTTGCTCGGGCTGGTCTCGA CA C DYNC1H1 Ensembl:ENSG00000197102 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1349216968 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_12270657 7117 RMVar_ID_7117 Human_SNP_ID_567720468 A-to-I Human chr14 + 102052333 102052333 102052333 TTTTGTATCTTTTGTAGAGACAAGGTTTCACCATGTTGCTCGGGCTGGTCTCGAACTCCTGAGCT TTTTGTATCTTTTGTAGAGACAAGGTTTCACCGTGTTGCTCGGGCTGGTCTCGAACTCCTGAGCT A G DYNC1H1 Ensembl:ENSG00000197102 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1268538383 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25082814 7118 RMVar_ID_7118 Human_SNP_ID_567730857 A-to-I Human chr14 - 102083543 102083543 102083543 AGAACCAGAAACATATCTATTATATCACAGGTAAGAGAACACTATGTTACAGTCATACACGTCGT AGAACCAGAAACATATCTATTATATCACAGGTGAGAGAACACTATGTTACAGTCATACACGTCGT T C HSP90AA1 Ensembl:ENSG00000080824 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs770713637 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1170958,Human_RBP_ID_1502649,Human_RBP_ID_1814616,Human_RBP_ID_2405413,Human_RBP_ID_3441600,Human_RBP_ID_6324582,Human_RBP_ID_8398940,Human_RBP_ID_8792786,Human_RBP_ID_12270952,Human_RBP_ID_17478266,Human_RBP_ID_18528750,Human_RBP_ID_18645154,Human_RBP_ID_19064382,Human_RBP_ID_22921129,Human_RBP_ID_26920205,Human_RBP_ID_27223780 RMVar_hsa_circ_74031,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_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 7119 RMVar_ID_7119 Human_SNP_ID_567736766 A-to-I Human chr14 - 102100039 102100039 102100039 AGACCACAGGCGCATGCCACCACTGCCTGGCTAATTTTTGTATTTTTTGTAAAGATGAGAGTTCC AGACCACAGGCGCATGCCACCACTGCCTGGCTGATTTTTGTATTTTTTGTAAAGATGAGAGTTCC T C HSP90AA1 Ensembl:ENSG00000080824 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1453465234 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102877,RMVar_hsa_circ_169368,RMVar_hsa_circ_16211 7120 RMVar_ID_7120 Human_SNP_ID_567745198 A-to-I Human chr14 - 102134249 102134249 102134249 TCCATGTCGGCTCTCTGCAACCTCCACCTCCTAGGCCCTGGCAAACCTCCCAAGTAGCTGGGACT TCCATGTCGGCTCTCTGCAACCTCCACCTCCTGGGCCCTGGCAAACCTCCCAAGTAGCTGGGACT T C HSP90AA1 Ensembl:ENSG00000080824 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs987460491 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102877,RMVar_hsa_circ_169368 7121 RMVar_ID_7121 Human_SNP_ID_567748377 A-to-I Human chr14 + 102144116 102144116 102144116 GAGGAGGGCTCTTGAGCCGAAGAGTTAAGGTTACAGTGAGCTATGATTGTGCCACTGTACCCCAA GAGGAGGGCTCTTGAGCCGAAGAGTTAAGGTTCCAGTGAGCTATGATTGTGCCACTGTACCCCAA A C WDR20 Ensembl:ENSG00000140153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749414634 Functional Loss SNV dbSNP153 33..33 33 - - - 7122 RMVar_ID_7122 Human_SNP_ID_567748905 A-to-I Human chr14 + 102146264 102146264 102146264 TGGCTCACTGTGACCTCTGGCACCCGGGTTTTAAGCGATTCTCCTGCCTCAGCCTCCGAAGTAGC TGGCTCACTGTGACCTCTGGCACCCGGGTTTTGAGCGATTCTCCTGCCTCAGCCTCCGAAGTAGC A G WDR20 Ensembl:ENSG00000140153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1168812416 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12271168 7123 RMVar_ID_7123 Human_SNP_ID_567748906 A-to-I Human chr14 + 102146264 102146264 102146264 TGGCTCACTGTGACCTCTGGCACCCGGGTTTTAAGCGATTCTCCTGCCTCAGCCTCCGAAGTAGC TGGCTCACTGTGACCTCTGGCACCCGGGTTTTTAGCGATTCTCCTGCCTCAGCCTCCGAAGTAGC A T WDR20 Ensembl:ENSG00000140153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1168812416 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12271168 7124 RMVar_ID_7124 Human_SNP_ID_567749726 A-to-I Human chr14 + 102149265 102149265 102149265 GTTGCCTAGTCTGACCTTGAACTCCTGGGCTCAAGTGATGCTTTTGCCTTGTGCTCCCAAAGTGC GTTGCCTAGTCTGACCTTGAACTCCTGGGCTCGAGTGATGCTTTTGCCTTGTGCTCCCAAAGTGC A G WDR20 Ensembl:ENSG00000140153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935102603 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23611680 7125 RMVar_ID_7125 Human_SNP_ID_567749987 A-to-I Human chr14 + 102150279 102150279 102150279 GGGAGGATTTCTTGAGGCTAGGAGTTGGAAACAAGCCTGGACAACATAGTGAGACCCCATCTCTA GGGAGGATTTCTTGAGGCTAGGAGTTGGAAACCAGCCTGGACAACATAGTGAGACCCCATCTCTA A C WDR20 Ensembl:ENSG00000140153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1184038497 Functional Loss SNV dbSNP153 33..33 33 - - - 7126 RMVar_ID_7126 Human_SNP_ID_567753134 A-to-I Human chr14 + 102162693 102162693 102162693 GGCTGGAGTGCAGTGTGATCTCAGCTCACTGCAACCTCTGCCTCCTGGGCTCAAGCCAGCCTCCC GGCTGGAGTGCAGTGTGATCTCAGCTCACTGCGACCTCTGCCTCCTGGGCTCAAGCCAGCCTCCC A G WDR20 Ensembl:ENSG00000140153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1462423395 Functional Loss SNV dbSNP153 33..33 33 - - - 7127 RMVar_ID_7127 Human_SNP_ID_567753182 A-to-I Human chr14 + 102162864 102162864 102162864 GAATTACTGGACTCAAGGTATCTGCCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG GAATTACTGGACTCAAGGTATCTGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG A G WDR20 Ensembl:ENSG00000140153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs767845320 Functional Loss SNV dbSNP153 33..33 33 - - - 7128 RMVar_ID_7128 Human_SNP_ID_567768225 A-to-I Human chr14 + 102220589 102220589 102220589 AAAACTACAAAAAGTTAGCTGGGCGTGGTGGCAGGCGCCTGTAGTCCAAGGTACTTGGGAGGCTG AAAACTACAAAAAGTTAGCTGGGCGTGGTGGCGGGCGCCTGTAGTCCAAGGTACTTGGGAGGCTG A G WDR20 Ensembl:ENSG00000140153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904295400 Functional Loss SNV dbSNP153 33..33 33 - - - 7129 RMVar_ID_7129 Human_SNP_ID_567768300 A-to-I Human chr14 + 102220796 102220795 102220797 TTTTTATTATCTATCTTTTCATTTTTTGAGACAGGGTCTTGCTCTATCCCCCAGGCTGGAGTGCA TTTTTATTATCTATCTTTTCATTTTTTGAGAC__GGTCTTGCTCTATCCCCCAGGCTGGAGTGCA CAG C WDR20 Ensembl:ENSG00000140153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1213513742 Functional Loss DEL dbSNP153 33..34 33 - - - 7130 RMVar_ID_7130 Human_SNP_ID_567768301 A-to-I Human chr14 + 102220796 102220796 102220796 TTTTTATTATCTATCTTTTCATTTTTTGAGACAGGGTCTTGCTCTATCCCCCAGGCTGGAGTGCA TTTTTATTATCTATCTTTTCATTTTTTGAGACGGGGTCTTGCTCTATCCCCCAGGCTGGAGTGCA A G WDR20 Ensembl:ENSG00000140153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1228214344 Functional Loss SNV dbSNP153 33..33 33 - - - 7131 RMVar_ID_7131 Human_SNP_ID_567768302 A-to-I Human chr14 + 102220796 102220796 102220796 TTTTTATTATCTATCTTTTCATTTTTTGAGACAGGGTCTTGCTCTATCCCCCAGGCTGGAGTGCA TTTTTATTATCTATCTTTTCATTTTTTGAGACTGGGTCTTGCTCTATCCCCCAGGCTGGAGTGCA A T WDR20 Ensembl:ENSG00000140153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1228214344 Functional Loss SNV dbSNP153 33..33 33 - - - 7132 RMVar_ID_7132 Human_SNP_ID_567768306 A-to-I Human chr14 + 102220809 102220809 102220809 TCTTTTCATTTTTTGAGACAGGGTCTTGCTCTATCCCCCAGGCTGGAGTGCAGTGGATCGCGGCT TCTTTTCATTTTTTGAGACAGGGTCTTGCTCTGTCCCCCAGGCTGGAGTGCAGTGGATCGCGGCT A G WDR20 Ensembl:ENSG00000140153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs754451163 Functional Loss SNV dbSNP153 33..33 33 - - - 7133 RMVar_ID_7133 Human_SNP_ID_567768328 A-to-I Human chr14 + 102220912 102220912 102220912 TGCCACACAGCCTCCTGAGTAGCTGGGATGACAGCCGTGCGCCACCACACCCGGCTAATTTTGTA TGCCACACAGCCTCCTGAGTAGCTGGGATGACGGCCGTGCGCCACCACACCCGGCTAATTTTGTA A G WDR20 Ensembl:ENSG00000140153 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1207496113 Functional Loss SNV dbSNP153 33..33 33 - - - 7134 RMVar_ID_7134 Human_SNP_ID_567783653 A-to-I Human chr14 - 102280124 102280124 102280124 CAGAAAGCAGATCCAGGATGTACCTCACCACCAGGAAACCATGTCCGTTAGGTAACCGCACACAC CAGAAAGCAGATCCAGGATGTACCTCACCACCGGGAAACCATGTCCGTTAGGTAACCGCACACAC T C MOK Ensembl:ENSG00000080823 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs895052812 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36672 7135 RMVar_ID_7135 Human_SNP_ID_567795629 A-to-I Human chr14 + 102322730 102322730 102322730 GGGGCTACATGTATGCACCATCATGCCTGGCTAATTTAAAAATGTTTTGTAGAGACAGGGTCCCG GGGGCTACATGTATGCACCATCATGCCTGGCTGATTTAAAAATGTTTTGTAGAGACAGGGTCCCG A G ZNF839 Ensembl:ENSG00000022976 Protein coding intron GSE38233;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;Bronchiolar epithelium,BERP35T4 cell line - 24183664,31158229 RNA-Seq:(High) rs35829645 Functional Loss SNV dbSNP153 33..33 33 - - - 7136 RMVar_ID_7136 Human_SNP_ID_567795983 A-to-I Human chr14 + 102324289 102324288 102324289 GGGTAACGCCGGGCACGGTGGTTCATGCCTGTAATCTCAGCACTTTGGGAGGCTGAGGCGGACAG GGGTAACGCCGGGCACGGTGGTTCATGCCTGT_ATCTCAGCACTTTGGGAGGCTGAGGCGGACAG TA T ZNF839 Ensembl:ENSG00000022976 Protein coding intron GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,31158229,31158229,31158229,31158229 RNA-Seq:(High) rs1338659612 Functional Loss DEL dbSNP153 33..33 33 - - - 7137 RMVar_ID_7137 Human_SNP_ID_567796071 A-to-I Human chr14 + 102324594 102324594 102324594 ATGGTGGCACACACCTGTGATCCCAGCTATTCAGTAGGCTGAGGCAGGAGAATCATTTGAACCTG ATGGTGGCACACACCTGTGATCCCAGCTATTCGGTAGGCTGAGGCAGGAGAATCATTTGAACCTG A G ZNF839 Ensembl:ENSG00000022976 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1187764352 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9757285 7138 RMVar_ID_7138 Human_SNP_ID_567796127 A-to-I Human chr14 + 102324819 102324819 102324819 AAAAATACAAAAATTAGCCGGGGCGTGGTGGTACGTGCCTGTAATCCCAGATACTTGGGAGACTG AAAAATACAAAAATTAGCCGGGGCGTGGTGGTGCGTGCCTGTAATCCCAGATACTTGGGAGACTG A G ZNF839 Ensembl:ENSG00000022976 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs966165919 Functional Loss SNV dbSNP153 33..33 33 - - - 7139 RMVar_ID_7139 Human_SNP_ID_567796248 A-to-I Human chr14 + 102325278 102325278 102325278 GAGAGAATCGCTGAAACTGGGAGGCAGAGGTTACAGTGAACTGAGATCGCACCACTGCACTCTAG GAGAGAATCGCTGAAACTGGGAGGCAGAGGTTGCAGTGAACTGAGATCGCACCACTGCACTCTAG A G ZNF839 Ensembl:ENSG00000022976 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs562198952 Functional Loss SNV dbSNP153 33..33 33 - - - 7140 RMVar_ID_7140 Human_SNP_ID_567798670 A-to-I Human chr14 + 102333352 102333352 102333352 TCAATCATGGCTCACTGCAGCCTCCACCTCCCAGGCTCAATTGATCTTCCTGCATCAGCCTCCCG TCAATCATGGCTCACTGCAGCCTCCACCTCCCGGGCTCAATTGATCTTCCTGCATCAGCCTCCCG A G ZNF839 Ensembl:ENSG00000022976 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs910694524 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5739,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_5642,RMVar_hsa_circ_43378,RMVar_hsa_circ_327534 7141 RMVar_ID_7141 Human_SNP_ID_567799325 A-to-I Human chr14 + 102335923 102335923 102335923 AAGAAGGGCCACGTGCAGTGGCTTATGCTTGTAGTCCCAGTGCTTTGGGAGACTGAGGCAGGTGG AAGAAGGGCCACGTGCAGTGGCTTATGCTTGTCGTCCCAGTGCTTTGGGAGACTGAGGCAGGTGG A C ZNF839 Ensembl:ENSG00000022976 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs545716237 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5739,RMVar_hsa_circ_286331,RMVar_hsa_circ_169398,RMVar_hsa_circ_5642,RMVar_hsa_circ_327534,RMVar_hsa_circ_47349,RMVar_hsa_circ_169399,RMVar_hsa_circ_368652 7142 RMVar_ID_7142 Human_SNP_ID_567800428 A-to-I Human chr14 + 102339487 102339487 102339487 GAGCCACAGGCCAGGTGCAGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCCGAGGTGGGC GAGCCACAGGCCAGGTGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGC A G ZNF839 Ensembl:ENSG00000022976 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1353469119 Functional Loss SNV dbSNP153 33..33 33 - - - 7143 RMVar_ID_7143 Human_SNP_ID_567802188 A-to-I Human chr14 - 102345922 102345922 102345922 ATGGTGCTGCATGCCTGTAATCCTAACTACTCAGGAGCCTGAGGCAGGAGAATCCCTTGAACCCG ATGGTGCTGCATGCCTGTAATCCTAACTACTCGGGAGCCTGAGGCAGGAGAATCCCTTGAACCCG T C CINP Ensembl:ENSG00000100865 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs950335314 Functional Loss SNV dbSNP153 33..33 33 - - - 7144 RMVar_ID_7144 Human_SNP_ID_567802352 A-to-I Human chr14 - 102346561 102346561 102346561 GGAGTGCAGTGGTGCAATCTCGGCTCATCACAACCTCCGCCTCCCGGGTTCAAGCGATTCTCCCC GGAGTGCAGTGGTGCAATCTCGGCTCATCACAGCCTCCGCCTCCCGGGTTCAAGCGATTCTCCCC T C CINP Ensembl:ENSG00000100865 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335337414 Functional Loss SNV dbSNP153 33..33 33 - - - 7145 RMVar_ID_7145 Human_SNP_ID_567802353 A-to-I Human chr14 - 102346564 102346564 102346564 GCTGGAGTGCAGTGGTGCAATCTCGGCTCATCACAACCTCCGCCTCCCGGGTTCAAGCGATTCTC GCTGGAGTGCAGTGGTGCAATCTCGGCTCATCGCAACCTCCGCCTCCCGGGTTCAAGCGATTCTC T C CINP Ensembl:ENSG00000100865 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941719931 Functional Loss SNV dbSNP153 33..33 33 - - - 7146 RMVar_ID_7146 Human_SNP_ID_567802370 A-to-I Human chr14 - 102346631 102346627 102346631 CTAAGTTTATTAAGACTATTGTAACTTTATTTATTTTTTGAGACAGAGTCTCGCTCTTGTTGCCC CTAAGTTTATTAAGACTATTGTAACTTTATTT____TTTGAGACAGAGTCTCGCTCTTGTTGCCC AAAAT A CINP Ensembl:ENSG00000100865 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1280843058 Functional Loss DEL dbSNP153 33..36 33 - - - 7147 RMVar_ID_7147 Human_SNP_ID_567802371 A-to-I Human chr14 - 102346631 102346631 102346631 CTAAGTTTATTAAGACTATTGTAACTTTATTTATTTTTTGAGACAGAGTCTCGCTCTTGTTGCCC CTAAGTTTATTAAGACTATTGTAACTTTATTTTTTTTTTGAGACAGAGTCTCGCTCTTGTTGCCC T A CINP Ensembl:ENSG00000100865 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs577360364 Functional Loss SNV dbSNP153 33..33 33 - - - 7148 RMVar_ID_7148 Human_SNP_ID_567802562 A-to-I Human chr14 - 102347459 102347459 102347459 CTCATGCCTCAGCCTCCAGAGTAGTTGGGACTACAGGCACGCGCCGCCACACCCAGCTAATGTTT CTCATGCCTCAGCCTCCAGAGTAGTTGGGACTGCAGGCACGCGCCGCCACACCCAGCTAATGTTT T C CINP Ensembl:ENSG00000100865 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs898767691 Functional Loss SNV dbSNP153 33..33 33 - - - 7149 RMVar_ID_7149 Human_SNP_ID_567802620 A-to-I Human chr14 - 102347649 102347649 102347649 GAGGGAAAGGTGACAGTTTTGAAACAGACCGAAGAGACTGGCCAAAAGCTAGGGCATGGGGAGAA GAGGGAAAGGTGACAGTTTTGAAACAGACCGAGGAGACTGGCCAAAAGCTAGGGCATGGGGAGAA T C CINP Ensembl:ENSG00000100865 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1051071339 Functional Loss SNV dbSNP153 33..33 33 - - - 7150 RMVar_ID_7150 Human_SNP_ID_567802704 A-to-I Human chr14 - 102348121 102348121 102348121 TTTTGGGCCAGGTGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGCGGA TTTTGGGCCAGGTGCGGTGGCTCATGCCTGTACTCCCAGCACTTTGGGAGGCCGAGGTGGGCGGA T G CINP Ensembl:ENSG00000100865 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1253224940 Functional Loss SNV dbSNP153 33..33 33 - - - 7151 RMVar_ID_7151 Human_SNP_ID_567804090 A-to-I Human chr14 - 102353967 102353967 102353967 TTCTTGCCTCAGCCTCCCGAGTAGCTGGGACTACAAGCATGAACCATCATGCCCGGCTAATTTTT TTCTTGCCTCAGCCTCCCGAGTAGCTGGGACTGCAAGCATGAACCATCATGCCCGGCTAATTTTT T C CINP Ensembl:ENSG00000100865 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1233040575 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_342880 7152 RMVar_ID_7152 Human_SNP_ID_567804095 A-to-I Human chr14 - 102353989 102353989 102353989 TACTTCCTGGGCTTAAGTGATCTTCTTGCCTCAGCCTCCCGAGTAGCTGGGACTACAAGCATGAA TACTTCCTGGGCTTAAGTGATCTTCTTGCCTCGGCCTCCCGAGTAGCTGGGACTACAAGCATGAA T C CINP Ensembl:ENSG00000100865 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1328342144 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_342880 7153 RMVar_ID_7153 Human_SNP_ID_567807028 A-to-I Human chr14 + 102365664 102365664 102365664 ATTATATGATTCAATTTTGATGAAATCTCCAGAATAGGCGAACTGTAGACAGAGAGGAGATCAGT ATTATATGATTCAATTTTGATGAAATCTCCAGCATAGGCGAACTGTAGACAGAGAGGAGATCAGT A C TECPR2 Ensembl:ENSG00000196663 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335824000 Functional Loss SNV dbSNP153 33..33 33 - - - 7154 RMVar_ID_7154 Human_SNP_ID_567807410 A-to-I Human chr14 + 102367475 102367475 102367475 CTGACCTACTCTGCCTACAGCTTGCCTATTCTAGACATTTTGTATACATGGAATCATATAATATA CTGACCTACTCTGCCTACAGCTTGCCTATTCTTGACATTTTGTATACATGGAATCATATAATATA A T TECPR2 Ensembl:ENSG00000196663 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs757565334 Functional Loss SNV dbSNP153 33..33 33 - - - 7155 RMVar_ID_7155 Human_SNP_ID_567807929 A-to-I Human chr14 + 102369564 102369564 102369564 CTTGTGCCTCAGCCTCCTGAGTAGATGGTACTACAGGCACGCACCACCACACCTGGCTACTTTTT CTTGTGCCTCAGCCTCCTGAGTAGATGGTACTGCAGGCACGCACCACCACACCTGGCTACTTTTT A G TECPR2 Ensembl:ENSG00000196663 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1003627077 Functional Loss SNV dbSNP153 33..33 33 - - - 7156 RMVar_ID_7156 Human_SNP_ID_567809799 A-to-I Human chr14 + 102377289 102377289 102377289 GTGATCCTTTTGCTTCAACTTCCTGAGTAGCTAGGACCACAGGGATGACTGCCACACCCAGCTAG GTGATCCTTTTGCTTCAACTTCCTGAGTAGCTGGGACCACAGGGATGACTGCCACACCCAGCTAG A G TECPR2 Ensembl:ENSG00000196663 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992167541 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45553,RMVar_hsa_circ_294672,RMVar_hsa_circ_320497,RMVar_hsa_circ_314981,RMVar_hsa_circ_288761,RMVar_hsa_circ_169403,RMVar_hsa_circ_169405,RMVar_hsa_circ_169407,RMVar_hsa_circ_35936,RMVar_hsa_circ_169406,RMVar_hsa_circ_169404 7157 RMVar_ID_7157 Human_SNP_ID_567809800 A-to-I Human chr14 + 102377289 102377289 102377289 GTGATCCTTTTGCTTCAACTTCCTGAGTAGCTAGGACCACAGGGATGACTGCCACACCCAGCTAG GTGATCCTTTTGCTTCAACTTCCTGAGTAGCTTGGACCACAGGGATGACTGCCACACCCAGCTAG A T TECPR2 Ensembl:ENSG00000196663 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992167541 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45553,RMVar_hsa_circ_294672,RMVar_hsa_circ_320497,RMVar_hsa_circ_314981,RMVar_hsa_circ_288761,RMVar_hsa_circ_169403,RMVar_hsa_circ_169405,RMVar_hsa_circ_169407,RMVar_hsa_circ_35936,RMVar_hsa_circ_169406,RMVar_hsa_circ_169404 7158 RMVar_ID_7158 Human_SNP_ID_567823933 A-to-I Human chr14 + 102432443 102432442 102432444 TGTATTTATATTATTTATTTATTTTTTGCGACAGAGTTTCGCTCGTCGCCCAGGCTGGAGTGCAA TGTATTTATATTATTTATTTATTTTTTGCGAC__AGTTTCGCTCGTCGCCCAGGCTGGAGTGCAA CAG C TECPR2 Ensembl:ENSG00000196663 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs780703227 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_45553,RMVar_hsa_circ_288761,RMVar_hsa_circ_169407,RMVar_hsa_circ_35936,RMVar_hsa_circ_22690,RMVar_hsa_circ_45590,RMVar_hsa_circ_127684,RMVar_hsa_circ_309868,RMVar_hsa_circ_169409,RMVar_hsa_circ_347375,RMVar_hsa_circ_72494,RMVar_hsa_circ_169410 7159 RMVar_ID_7159 Human_SNP_ID_567830556 A-to-I Human chr14 + 102457359 102457359 102457359 CACCCGTCTTGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACTGCGCCTGACCCAAGAGA CACCCGTCTTGGCCTCCCAAAGTGCTGGGATTCCAGGTGTGAGCCACTGCGCCTGACCCAAGAGA A C TECPR2 Ensembl:ENSG00000196663 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1440102696 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_288761,RMVar_hsa_circ_169407,RMVar_hsa_circ_22690,RMVar_hsa_circ_45590,RMVar_hsa_circ_127684,RMVar_hsa_circ_309868,RMVar_hsa_circ_169409,RMVar_hsa_circ_315379,RMVar_hsa_circ_169410,RMVar_hsa_circ_266060,RMVar_hsa_circ_169414,RMVar_hsa_circ_45748,RMVar_hsa_circ_266510 7160 RMVar_ID_7160 Human_SNP_ID_567835489 A-to-I Human chr14 + 102478534 102478534 102478534 GAAATCCCATCTCTATGAAAAATACAAAAGTTAGCCAGGTGTGGTGGCATGTGCCTGTAGTTCCA GAAATCCCATCTCTATGAAAAATACAAAAGTTGGCCAGGTGTGGTGGCATGTGCCTGTAGTTCCA A G TECPR2 Ensembl:ENSG00000196663 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031138080 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127684,RMVar_hsa_circ_169409,RMVar_hsa_circ_266510 7161 RMVar_ID_7161 Human_SNP_ID_567868563 A-to-I Human chr14 + 102595233 102595233 102595233 TCTAAAATGGAAAACATTTATCAGATTGCAGTAGCTCACACCTGTAGTCCCAACACTTGGGGAGG TCTAAAATGGAAAACATTTATCAGATTGCAGTTGCTCACACCTGTAGTCCCAACACTTGGGGAGG A T RCOR1 Ensembl:ENSG00000089902 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs892501824 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12274174 7162 RMVar_ID_7162 Human_SNP_ID_567868565 A-to-I Human chr14 + 102595240 102595240 102595240 TGGAAAACATTTATCAGATTGCAGTAGCTCACACCTGTAGTCCCAACACTTGGGGAGGCCAAGGC TGGAAAACATTTATCAGATTGCAGTAGCTCACGCCTGTAGTCCCAACACTTGGGGAGGCCAAGGC A G RCOR1 Ensembl:ENSG00000089902 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893774514 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12274174 7163 RMVar_ID_7163 Human_SNP_ID_567868574 A-to-I Human chr14 + 102595268 102595268 102595268 TCACACCTGTAGTCCCAACACTTGGGGAGGCCAAGGCTGGAGGATCTCTGGAGCTCAGGAGTTGG TCACACCTGTAGTCCCAACACTTGGGGAGGCCCAGGCTGGAGGATCTCTGGAGCTCAGGAGTTGG A C RCOR1 Ensembl:ENSG00000089902 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1397152812 Functional Loss SNV dbSNP153 33..33 33 - - - 7164 RMVar_ID_7164 Human_SNP_ID_567868580 A-to-I Human chr14 + 102595292 102595292 102595292 GGGAGGCCAAGGCTGGAGGATCTCTGGAGCTCAGGAGTTGGAGACCAGCCTGGGCAATGTAGTCA GGGAGGCCAAGGCTGGAGGATCTCTGGAGCTCGGGAGTTGGAGACCAGCCTGGGCAATGTAGTCA A G RCOR1 Ensembl:ENSG00000089902 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1298763519 Functional Loss SNV dbSNP153 33..33 33 - - - 7165 RMVar_ID_7165 Human_SNP_ID_567868595 A-to-I Human chr14 + 102595346 102595345 102595346 CAATGTAGTCAGACTCTGTCTCAACAAAAAATAAAAAAATTAGCTGGGCATGGTGGCATGTGCCT CAATGTAGTCAGACTCTGTCTCAACAAAAAAT_AAAAAATTAGCTGGGCATGGTGGCATGTGCCT TA T RCOR1 Ensembl:ENSG00000089902 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1014291134 Functional Loss DEL dbSNP153 33..33 33 - - - 7166 RMVar_ID_7166 Human_SNP_ID_567870536 A-to-I Human chr14 + 102601164 102601164 102601164 TGAGCGTAGATGGCACCACTGCACTCCAGCCTAGGTGACAAAGTGAGACTCTGTCTCAAAAAAAA TGAGCGTAGATGGCACCACTGCACTCCAGCCTGGGTGACAAAGTGAGACTCTGTCTCAAAAAAAA A G RCOR1 Ensembl:ENSG00000089902 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs865833858 Functional Loss SNV dbSNP153 33..33 33 - - - 7167 RMVar_ID_7167 Human_SNP_ID_567870556 A-to-I Human chr14 + 102601247 102601247 102601247 GGTGGCCAGGCTGGTTTCGAACTCTTGACCTCAGGTGATTGACCCGCCTTGGCCTCCCAAAGTGC GGTGGCCAGGCTGGTTTCGAACTCTTGACCTCCGGTGATTGACCCGCCTTGGCCTCCCAAAGTGC A C RCOR1 Ensembl:ENSG00000089902 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs959470112 Functional Loss SNV dbSNP153 33..33 33 - - - 7168 RMVar_ID_7168 Human_SNP_ID_567871299 A-to-I Human chr14 + 102603690 102603690 102603690 TTGCCCAGGCTGGAGTGCGGTGGCTTAATCTCAGCTCACTGCAACCTTCATCTCCTGGGCTCACA TTGCCCAGGCTGGAGTGCGGTGGCTTAATCTCGGCTCACTGCAACCTTCATCTCCTGGGCTCACA A G RCOR1 Ensembl:ENSG00000089902 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1021738694 Functional Loss SNV dbSNP153 33..33 33 - - - 7169 RMVar_ID_7169 Human_SNP_ID_567877437 A-to-I Human chr14 + 102624460 102624460 102624460 CCAGGAGGCAGAGGTTACAGTGAGCCAAGATCATGCCAACTGCACTCCAGCCTGGGCATCAGTCT CCAGGAGGCAGAGGTTACAGTGAGCCAAGATCGTGCCAACTGCACTCCAGCCTGGGCATCAGTCT A G RCOR1 Ensembl:ENSG00000089902 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1414051623 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17562641,Human_RBP_ID_23306997 7170 RMVar_ID_7170 Human_SNP_ID_567877631 A-to-I Human chr14 + 102625109 102625109 102625109 GTTGCCCAGGCTGGTCTGGAACTCCTCACCTCAAGGGATCCTCTTGCCTGGGCCTCCCAAAGTGT GTTGCCCAGGCTGGTCTGGAACTCCTCACCTCGAGGGATCCTCTTGCCTGGGCCTCCCAAAGTGT A G RCOR1 Ensembl:ENSG00000089902 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs922625661 Functional Loss SNV dbSNP153 33..33 33 - - - 7171 RMVar_ID_7171 Human_SNP_ID_567878200 A-to-I Human chr14 + 102627393 102627393 102627393 TTTAAAAACTTTTTTGCCGGGTGTGGTGGCTCACGCCCGTAATCCCAACACTTTGGGAGGCCAAG TTTAAAAACTTTTTTGCCGGGTGTGGTGGCTCTCGCCCGTAATCCCAACACTTTGGGAGGCCAAG A T RCOR1 Ensembl:ENSG00000089902 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1219085233 Functional Loss SNV dbSNP153 33..33 33 - - - 7172 RMVar_ID_7172 Human_SNP_ID_567880763 A-to-I Human chr14 + 102635393 102635393 102635393 GGGTGTCATGGCAGGTGCCTGTATTCCCAGCTACTCGGGAGGCTGAGGTGGGAGAACTGCTTGAA GGGTGTCATGGCAGGTGCCTGTATTCCCAGCTTCTCGGGAGGCTGAGGTGGGAGAACTGCTTGAA A T RCOR1 Ensembl:ENSG00000089902 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1416188902 Functional Loss SNV dbSNP153 33..33 33 - - - 7173 RMVar_ID_7173 Human_SNP_ID_567882375 A-to-I Human chr14 + 102640746 102640746 102640746 CCTGTAATTCCAGCATTTTGGGAGACTGAGGTAGGAGGGACACTTGAGCCCAGCCTGGGCAACAT CCTGTAATTCCAGCATTTTGGGAGACTGAGGTGGGAGGGACACTTGAGCCCAGCCTGGGCAACAT A G RCOR1 Ensembl:ENSG00000089902 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1187307950 Functional Loss SNV dbSNP153 33..33 33 - - - 7174 RMVar_ID_7174 Human_SNP_ID_567886963 A-to-I Human chr14 + 102657717 102657717 102657717 AAAATTAGCCGGACTTGGTGGTGCGTGCCTGTAATCCCAGCTACTGGGGAGACAGAGGTGAGAGA AAAATTAGCCGGACTTGGTGGTGCGTGCCTGTGATCCCAGCTACTGGGGAGACAGAGGTGAGAGA A G RCOR1 Ensembl:ENSG00000089902 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs750705657 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12275037 7175 RMVar_ID_7175 Human_SNP_ID_567890338 A-to-I Human chr14 + 102671473 102671473 102671473 GCTGGAGTGCAGCAGGGTGATCATAGCTCACTACAGCCTTGAACTCTTGGGCTCAAGCAATCCTT GCTGGAGTGCAGCAGGGTGATCATAGCTCACTGCAGCCTTGAACTCTTGGGCTCAAGCAATCCTT A G RCOR1 Ensembl:ENSG00000089902 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1050133600 Functional Loss SNV dbSNP153 33..33 33 - - - 7176 RMVar_ID_7176 Human_SNP_ID_567905423 A-to-I Human chr14 + 102725652 102725652 102725652 GCAAGTGGAGTGCAGTGGTACGATCTTAGCTCACTGCAGCCTCCATCTCCCGAGCTCTTGATTCT GCAAGTGGAGTGCAGTGGTACGATCTTAGCTCTCTGCAGCCTCCATCTCCCGAGCTCTTGATTCT A T RCOR1 Ensembl:ENSG00000089902 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs201177379 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1360819 7177 RMVar_ID_7177 Human_SNP_ID_567905596 A-to-I Human chr14 + 102726206 102726206 102726206 AAAATTAGCTGGGCGTGGAGGCAGGTGCCTGTAGTTGCGGCTACTTGAGAGGCTGAGGCAGAGGA AAAATTAGCTGGGCGTGGAGGCAGGTGCCTGTGGTTGCGGCTACTTGAGAGGCTGAGGCAGAGGA A G RCOR1 Ensembl:ENSG00000089902 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs562865831 Functional Loss SNV dbSNP153 33..33 33 - - - 7178 RMVar_ID_7178 Human_SNP_ID_567908099 A-to-I Human chr14 + 102735364 102735364 102735364 TTTTGTATTTTTAGTAGAGACGGGGTTTCTCCATGCTGCCCAGGCTAGTCTTGAACTCCTGACCT TTTTGTATTTTTAGTAGAGACGGGGTTTCTCCCTGCTGCCCAGGCTAGTCTTGAACTCCTGACCT A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1339293228 Functional Loss SNV dbSNP153 33..33 33 - - - 7179 RMVar_ID_7179 Human_SNP_ID_567922107 A-to-I Human chr14 + 102784322 102784322 102784322 TCGACTCACTGCAACCTCCGCCCCCTGGGTTCAAGCTATTCTCCTGCCCCAGCCTCCTGAGTAGC TCGACTCACTGCAACCTCCGCCCCCTGGGTTCGAGCTATTCTCCTGCCCCAGCCTCCTGAGTAGC A G TRAF3 Ensembl:ENSG00000131323 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs375087493 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18645512 RMVar_hsa_circ_92668,RMVar_hsa_circ_95533,RMVar_hsa_circ_169427,RMVar_hsa_circ_169428 7180 RMVar_ID_7180 Human_SNP_ID_567922766 A-to-I Human chr14 + 102786933 102786933 102786933 GGAGGAGTGCTTGAGCCCAGGAGGTCGAGGCTACAGTGAGGTGTTACTGTGTCACCATACTTCCG GGAGGAGTGCTTGAGCCCAGGAGGTCGAGGCTGCAGTGAGGTGTTACTGTGTCACCATACTTCCG A G TRAF3 Ensembl:ENSG00000131323 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs545064729 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92668,RMVar_hsa_circ_95533,RMVar_hsa_circ_169427,RMVar_hsa_circ_169428 7181 RMVar_ID_7181 Human_SNP_ID_567923065 A-to-I Human chr14 + 102787991 102787991 102787991 CTCATGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGTATGCACCACCCCACCTGGCTAATTTTT CTCATGCCTCAGCCTCCCGAGTAGCTGGGATTGCAGGTATGCACCACCCCACCTGGCTAATTTTT A G TRAF3 Ensembl:ENSG00000131323 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs774222916 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92668,RMVar_hsa_circ_95533,RMVar_hsa_circ_169427,RMVar_hsa_circ_169428 7182 RMVar_ID_7182 Human_SNP_ID_567923084 A-to-I Human chr14 + 102788034 102788034 102788034 CCACCCCACCTGGCTAATTTTTGTATTTTTTTAGTAGAGACAGGGTTTCACCATTGTTGACCAGG CCACCCCACCTGGCTAATTTTTGTATTTTTTTGGTAGAGACAGGGTTTCACCATTGTTGACCAGG A G TRAF3 Ensembl:ENSG00000131323 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1336920191 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92668,RMVar_hsa_circ_95533,RMVar_hsa_circ_169427,RMVar_hsa_circ_169428 7183 RMVar_ID_7183 Human_SNP_ID_567924502 A-to-I Human chr14 + 102793280 102793280 102793280 CTCAAGTGGTCCTCCCACCCAGCTGCCTGAGTAGCTGGTACTACAGGCACTTGCCACCACACCCA CTCAAGTGGTCCTCCCACCCAGCTGCCTGAGTGGCTGGTACTACAGGCACTTGCCACCACACCCA A G TRAF3 Ensembl:ENSG00000131323 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs903787730 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_441561 RMVar_hsa_circ_92668,RMVar_hsa_circ_95533,RMVar_hsa_circ_169427,RMVar_hsa_circ_169428 7184 RMVar_ID_7184 Human_SNP_ID_567926697 A-to-I Human chr14 + 102801593 102801593 102801593 GTCTCACTCTGTCACCCAGGCTGAGGTGCAGTAGTACAATCACAGCTCACTGCAGCCTCGATTTC GTCTCACTCTGTCACCCAGGCTGAGGTGCAGTCGTACAATCACAGCTCACTGCAGCCTCGATTTC A C TRAF3 Ensembl:ENSG00000131323 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs990464988 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92668,RMVar_hsa_circ_95533,RMVar_hsa_circ_169427,RMVar_hsa_circ_169428 7185 RMVar_ID_7185 Human_SNP_ID_567927553 A-to-I Human chr14 + 102804587 102804587 102804587 TCAGCTCACAGGAGCATCAACCTCCTGGGCTCAAGTGATCCTCCCACCTCAGCCTCCCAAGTAGC TCAGCTCACAGGAGCATCAACCTCCTGGGCTCGAGTGATCCTCCCACCTCAGCCTCCCAAGTAGC A G TRAF3 Ensembl:ENSG00000131323 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1008240709 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92668,RMVar_hsa_circ_95533,RMVar_hsa_circ_169427,RMVar_hsa_circ_169428 7186 RMVar_ID_7186 Human_SNP_ID_567927558 A-to-I Human chr14 + 102804613 102804613 102804613 GGGCTCAAGTGATCCTCCCACCTCAGCCTCCCAAGTAGCTGGAACTACAGGTGCAAGCCACCACA GGGCTCAAGTGATCCTCCCACCTCAGCCTCCCGAGTAGCTGGAACTACAGGTGCAAGCCACCACA A G TRAF3 Ensembl:ENSG00000131323 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1450567775 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92668,RMVar_hsa_circ_95533,RMVar_hsa_circ_169427,RMVar_hsa_circ_169428 7187 RMVar_ID_7187 Human_SNP_ID_567937292 A-to-I Human chr14 + 102841987 102841987 102841987 ATATAAAATGCCGGGCGCAGTGGCTCACACCTATAATCCCAATTCTTTGGGAGGCTGAGGTGGGC ATATAAAATGCCGGGCGCAGTGGCTCACACCTGTAATCCCAATTCTTTGGGAGGCTGAGGTGGGC A G TRAF3 Ensembl:ENSG00000131323 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs373195547 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_169430,RMVar_hsa_circ_92668,RMVar_hsa_circ_95533,RMVar_hsa_circ_273169,RMVar_hsa_circ_169427,RMVar_hsa_circ_169428,RMVar_hsa_circ_309358,RMVar_hsa_circ_318210,RMVar_hsa_circ_276988,RMVar_hsa_circ_169432,RMVar_hsa_circ_23381,RMVar_hsa_circ_169431,RMVar_hsa_circ_169429 7188 RMVar_ID_7188 Human_SNP_ID_567937730 A-to-I Human chr14 + 102843590 102843590 102843590 GAACTCCTGATTTCAAGCAATCCACCCATCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG GAACTCCTGATTTCAAGCAATCCACCCATCTCCGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG A C TRAF3 Ensembl:ENSG00000131323 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1225298230 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_169430,RMVar_hsa_circ_92668,RMVar_hsa_circ_95533,RMVar_hsa_circ_273169,RMVar_hsa_circ_169427,RMVar_hsa_circ_169428,RMVar_hsa_circ_309358,RMVar_hsa_circ_318210,RMVar_hsa_circ_276988,RMVar_hsa_circ_169432,RMVar_hsa_circ_23381,RMVar_hsa_circ_169431,RMVar_hsa_circ_169429 7189 RMVar_ID_7189 Human_SNP_ID_567937731 A-to-I Human chr14 + 102843590 102843590 102843590 GAACTCCTGATTTCAAGCAATCCACCCATCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG GAACTCCTGATTTCAAGCAATCCACCCATCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG A G TRAF3 Ensembl:ENSG00000131323 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1225298230 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_169430,RMVar_hsa_circ_92668,RMVar_hsa_circ_95533,RMVar_hsa_circ_273169,RMVar_hsa_circ_169427,RMVar_hsa_circ_169428,RMVar_hsa_circ_309358,RMVar_hsa_circ_318210,RMVar_hsa_circ_276988,RMVar_hsa_circ_169432,RMVar_hsa_circ_23381,RMVar_hsa_circ_169431,RMVar_hsa_circ_169429 7190 RMVar_ID_7190 Human_SNP_ID_567943160 A-to-I Human chr14 + 102865578 102865578 102865578 CTGGAGTGCAGTGGCACGATCTCGGGTCACTGAAACCTCTGCCTCCCAGGTTCAAGCAATTCTCC CTGGAGTGCAGTGGCACGATCTCGGGTCACTGGAACCTCTGCCTCCCAGGTTCAAGCAATTCTCC A G TRAF3 Ensembl:ENSG00000131323 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs897973525 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_169430,RMVar_hsa_circ_92668,RMVar_hsa_circ_95533,RMVar_hsa_circ_273169,RMVar_hsa_circ_169427,RMVar_hsa_circ_169428,RMVar_hsa_circ_309358,RMVar_hsa_circ_318210,RMVar_hsa_circ_276988,RMVar_hsa_circ_169432,RMVar_hsa_circ_23381,RMVar_hsa_circ_169431,RMVar_hsa_circ_169429 7191 RMVar_ID_7191 Human_SNP_ID_567943161 A-to-I Human chr14 + 102865578 102865578 102865578 CTGGAGTGCAGTGGCACGATCTCGGGTCACTGAAACCTCTGCCTCCCAGGTTCAAGCAATTCTCC CTGGAGTGCAGTGGCACGATCTCGGGTCACTGTAACCTCTGCCTCCCAGGTTCAAGCAATTCTCC A T TRAF3 Ensembl:ENSG00000131323 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs897973525 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_169430,RMVar_hsa_circ_92668,RMVar_hsa_circ_95533,RMVar_hsa_circ_273169,RMVar_hsa_circ_169427,RMVar_hsa_circ_169428,RMVar_hsa_circ_309358,RMVar_hsa_circ_318210,RMVar_hsa_circ_276988,RMVar_hsa_circ_169432,RMVar_hsa_circ_23381,RMVar_hsa_circ_169431,RMVar_hsa_circ_169429 7192 RMVar_ID_7192 Human_SNP_ID_567945662 A-to-I Human chr14 + 102874846 102874846 102874846 AGCTAATTTTTTAAAAAAATTTTTGTAGAGATAGGGTCTCATTGTGTTGCCTAGGCTGGTCTCAA AGCTAATTTTTTAAAAAAATTTTTGTAGAGATGGGGTCTCATTGTGTTGCCTAGGCTGGTCTCAA A G TRAF3 Ensembl:ENSG00000131323 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1038627995 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_169430,RMVar_hsa_circ_92668,RMVar_hsa_circ_95533,RMVar_hsa_circ_273169,RMVar_hsa_circ_169427,RMVar_hsa_circ_169428,RMVar_hsa_circ_309358,RMVar_hsa_circ_318210,RMVar_hsa_circ_276988,RMVar_hsa_circ_169432,RMVar_hsa_circ_23381,RMVar_hsa_circ_169431,RMVar_hsa_circ_28884,RMVar_hsa_circ_285399,RMVar_hsa_circ_297681,RMVar_hsa_circ_336338,RMVar_hsa_circ_169429,RMVar_hsa_circ_297188,RMVar_hsa_circ_273716,RMVar_hsa_circ_169435,RMVar_hsa_circ_169437,RMVar_hsa_circ_169438,RMVar_hsa_circ_169436,RMVar_hsa_circ_169434,RMVar_hsa_circ_169439,RMVar_hsa_circ_100298 7193 RMVar_ID_7193 Human_SNP_ID_567947212 A-to-I Human chr14 + 102879823 102879823 102879823 CTTGTGTGGTACTTCAGATGTTTCCAGTTATTAAGAACTCTTGAGGCTGGGTGTGGTAGCTCACA CTTGTGTGGTACTTCAGATGTTTCCAGTTATTGAGAACTCTTGAGGCTGGGTGTGGTAGCTCACA A G TRAF3 Ensembl:ENSG00000131323 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs944274887 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12277507 RMVar_hsa_circ_2753,RMVar_hsa_circ_169430,RMVar_hsa_circ_95533,RMVar_hsa_circ_273169,RMVar_hsa_circ_169428,RMVar_hsa_circ_309358,RMVar_hsa_circ_318210,RMVar_hsa_circ_23381,RMVar_hsa_circ_169431,RMVar_hsa_circ_28884,RMVar_hsa_circ_297681,RMVar_hsa_circ_336338,RMVar_hsa_circ_169429,RMVar_hsa_circ_297188,RMVar_hsa_circ_273716,RMVar_hsa_circ_169435,RMVar_hsa_circ_169437,RMVar_hsa_circ_169438,RMVar_hsa_circ_169436,RMVar_hsa_circ_64275,RMVar_hsa_circ_169439,RMVar_hsa_circ_100298,RMVar_hsa_circ_9633 7194 RMVar_ID_7194 Human_SNP_ID_567947218 A-to-I Human chr14 + 102879855 102879843 102879855 AAGAACTCTTGAGGCTGGGTGTGGTAGCTCACACCTGTGTGCCCAGCACTTTGGGAGGCTGAAAC AAGAACTCTTGAGGCTGGGTG____________CCTGTGTGCCCAGCACTTTGGGAGGCTGAAAC GTGGTAGCTCACA G TRAF3 Ensembl:ENSG00000131323 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1262694140 Functional Loss DEL dbSNP153 22..33 33 - - - RMVar_hsa_circ_2753,RMVar_hsa_circ_169430,RMVar_hsa_circ_95533,RMVar_hsa_circ_273169,RMVar_hsa_circ_169428,RMVar_hsa_circ_309358,RMVar_hsa_circ_318210,RMVar_hsa_circ_23381,RMVar_hsa_circ_169431,RMVar_hsa_circ_28884,RMVar_hsa_circ_297681,RMVar_hsa_circ_336338,RMVar_hsa_circ_169429,RMVar_hsa_circ_297188,RMVar_hsa_circ_273716,RMVar_hsa_circ_169435,RMVar_hsa_circ_169437,RMVar_hsa_circ_169438,RMVar_hsa_circ_169436,RMVar_hsa_circ_64275,RMVar_hsa_circ_169439,RMVar_hsa_circ_100298,RMVar_hsa_circ_9633 7195 RMVar_ID_7195 Human_SNP_ID_567948204 A-to-I Human chr14 + 102883689 102883689 102883689 CTCACTGTAACCTTCGCCTCCCAGGTTCAAGCAATTTTCCTGCCTCAGCCTCACGAGTAGCTGGG CTCACTGTAACCTTCGCCTCCCAGGTTCAAGCGATTTTCCTGCCTCAGCCTCACGAGTAGCTGGG A G TRAF3 Ensembl:ENSG00000131323 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1482272219 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2753,RMVar_hsa_circ_169430,RMVar_hsa_circ_95533,RMVar_hsa_circ_273169,RMVar_hsa_circ_169428,RMVar_hsa_circ_309358,RMVar_hsa_circ_318210,RMVar_hsa_circ_23381,RMVar_hsa_circ_169431,RMVar_hsa_circ_28884,RMVar_hsa_circ_297681,RMVar_hsa_circ_336338,RMVar_hsa_circ_169429,RMVar_hsa_circ_297188,RMVar_hsa_circ_273716,RMVar_hsa_circ_169435,RMVar_hsa_circ_169437,RMVar_hsa_circ_169438,RMVar_hsa_circ_169436,RMVar_hsa_circ_64275,RMVar_hsa_circ_169439,RMVar_hsa_circ_100298,RMVar_hsa_circ_9633 7196 RMVar_ID_7196 Human_SNP_ID_567948205 A-to-I Human chr14 + 102883689 102883689 102883689 CTCACTGTAACCTTCGCCTCCCAGGTTCAAGCAATTTTCCTGCCTCAGCCTCACGAGTAGCTGGG CTCACTGTAACCTTCGCCTCCCAGGTTCAAGCTATTTTCCTGCCTCAGCCTCACGAGTAGCTGGG A T TRAF3 Ensembl:ENSG00000131323 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1482272219 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2753,RMVar_hsa_circ_169430,RMVar_hsa_circ_95533,RMVar_hsa_circ_273169,RMVar_hsa_circ_169428,RMVar_hsa_circ_309358,RMVar_hsa_circ_318210,RMVar_hsa_circ_23381,RMVar_hsa_circ_169431,RMVar_hsa_circ_28884,RMVar_hsa_circ_297681,RMVar_hsa_circ_336338,RMVar_hsa_circ_169429,RMVar_hsa_circ_297188,RMVar_hsa_circ_273716,RMVar_hsa_circ_169435,RMVar_hsa_circ_169437,RMVar_hsa_circ_169438,RMVar_hsa_circ_169436,RMVar_hsa_circ_64275,RMVar_hsa_circ_169439,RMVar_hsa_circ_100298,RMVar_hsa_circ_9633 7197 RMVar_ID_7197 Human_SNP_ID_567949029 A-to-I Human chr14 + 102886635 102886635 102886635 AAAACTAGCCAGGTGTGGTGGCGCGCACCTGTAATCCCAGCTATTCAGGAGGCCGAGGCAGGAGA AAAACTAGCCAGGTGTGGTGGCGCGCACCTGTGATCCCAGCTATTCAGGAGGCCGAGGCAGGAGA A G TRAF3 Ensembl:ENSG00000131323 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1334359959 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2753,RMVar_hsa_circ_169430,RMVar_hsa_circ_273169,RMVar_hsa_circ_309358,RMVar_hsa_circ_318210,RMVar_hsa_circ_169431,RMVar_hsa_circ_28884,RMVar_hsa_circ_297681,RMVar_hsa_circ_169429,RMVar_hsa_circ_297188,RMVar_hsa_circ_273716,RMVar_hsa_circ_169437,RMVar_hsa_circ_169438,RMVar_hsa_circ_169436,RMVar_hsa_circ_9633,RMVar_hsa_circ_169441,RMVar_hsa_circ_109812,RMVar_hsa_circ_325489,RMVar_hsa_circ_349615,RMVar_hsa_circ_301249,RMVar_hsa_circ_169442,RMVar_hsa_circ_169440 7198 RMVar_ID_7198 Human_SNP_ID_567949034 A-to-I Human chr14 + 102886649 102886649 102886649 GTGGTGGCGCGCACCTGTAATCCCAGCTATTCAGGAGGCCGAGGCAGGAGAATCATTTGAACCGG GTGGTGGCGCGCACCTGTAATCCCAGCTATTCCGGAGGCCGAGGCAGGAGAATCATTTGAACCGG A C TRAF3 Ensembl:ENSG00000131323 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1442060338 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2753,RMVar_hsa_circ_169430,RMVar_hsa_circ_273169,RMVar_hsa_circ_309358,RMVar_hsa_circ_318210,RMVar_hsa_circ_169431,RMVar_hsa_circ_28884,RMVar_hsa_circ_297681,RMVar_hsa_circ_169429,RMVar_hsa_circ_297188,RMVar_hsa_circ_273716,RMVar_hsa_circ_169437,RMVar_hsa_circ_169438,RMVar_hsa_circ_169436,RMVar_hsa_circ_9633,RMVar_hsa_circ_169441,RMVar_hsa_circ_109812,RMVar_hsa_circ_325489,RMVar_hsa_circ_349615,RMVar_hsa_circ_301249,RMVar_hsa_circ_169442,RMVar_hsa_circ_169440 7199 RMVar_ID_7199 Human_SNP_ID_567949302 A-to-I Human chr14 + 102887712 102887712 102887712 TGCCTCCTGGGTTCACACCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCTG TGCCTCCTGGGTTCACACCATTCTCCTGCCTCGGCCTCCCGAGTAGCTGGGACTACAGGCGCCTG A G TRAF3 Ensembl:ENSG00000131323 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs898396379 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2753,RMVar_hsa_circ_169430,RMVar_hsa_circ_273169,RMVar_hsa_circ_309358,RMVar_hsa_circ_318210,RMVar_hsa_circ_169431,RMVar_hsa_circ_28884,RMVar_hsa_circ_297681,RMVar_hsa_circ_169429,RMVar_hsa_circ_297188,RMVar_hsa_circ_273716,RMVar_hsa_circ_169437,RMVar_hsa_circ_169438,RMVar_hsa_circ_169436,RMVar_hsa_circ_9633,RMVar_hsa_circ_169441,RMVar_hsa_circ_109812,RMVar_hsa_circ_325489,RMVar_hsa_circ_349615,RMVar_hsa_circ_301249,RMVar_hsa_circ_169442,RMVar_hsa_circ_169440 7200 RMVar_ID_7200 Human_SNP_ID_567949318 A-to-I Human chr14 + 102887760 102887760 102887760 GGGACTACAGGCGCCTGCCACCACGCCCGGCTAATTTCTTGTATTTTTTAGTAGAGACGGGGTTT GGGACTACAGGCGCCTGCCACCACGCCCGGCTGATTTCTTGTATTTTTTAGTAGAGACGGGGTTT A G TRAF3 Ensembl:ENSG00000131323 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1270211965 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2753,RMVar_hsa_circ_169430,RMVar_hsa_circ_273169,RMVar_hsa_circ_309358,RMVar_hsa_circ_318210,RMVar_hsa_circ_169431,RMVar_hsa_circ_28884,RMVar_hsa_circ_297681,RMVar_hsa_circ_169429,RMVar_hsa_circ_297188,RMVar_hsa_circ_273716,RMVar_hsa_circ_169437,RMVar_hsa_circ_169438,RMVar_hsa_circ_169436,RMVar_hsa_circ_9633,RMVar_hsa_circ_169441,RMVar_hsa_circ_109812,RMVar_hsa_circ_325489,RMVar_hsa_circ_349615,RMVar_hsa_circ_301249,RMVar_hsa_circ_169442,RMVar_hsa_circ_169440 7201 RMVar_ID_7201 Human_SNP_ID_567949322 A-to-I Human chr14 + 102887777 102887777 102887777 CCACCACGCCCGGCTAATTTCTTGTATTTTTTAGTAGAGACGGGGTTTCACCTTGTTAGCCAGCA CCACCACGCCCGGCTAATTTCTTGTATTTTTTGGTAGAGACGGGGTTTCACCTTGTTAGCCAGCA A G TRAF3 Ensembl:ENSG00000131323 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs979566747 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2753,RMVar_hsa_circ_169430,RMVar_hsa_circ_273169,RMVar_hsa_circ_309358,RMVar_hsa_circ_318210,RMVar_hsa_circ_169431,RMVar_hsa_circ_28884,RMVar_hsa_circ_297681,RMVar_hsa_circ_169429,RMVar_hsa_circ_297188,RMVar_hsa_circ_273716,RMVar_hsa_circ_169437,RMVar_hsa_circ_169438,RMVar_hsa_circ_169436,RMVar_hsa_circ_9633,RMVar_hsa_circ_169441,RMVar_hsa_circ_109812,RMVar_hsa_circ_325489,RMVar_hsa_circ_349615,RMVar_hsa_circ_301249,RMVar_hsa_circ_169442,RMVar_hsa_circ_169440 7202 RMVar_ID_7202 Human_SNP_ID_567949323 A-to-I Human chr14 + 102887780 102887780 102887780 CCACGCCCGGCTAATTTCTTGTATTTTTTAGTAGAGACGGGGTTTCACCTTGTTAGCCAGCATGG CCACGCCCGGCTAATTTCTTGTATTTTTTAGTGGAGACGGGGTTTCACCTTGTTAGCCAGCATGG A G TRAF3 Ensembl:ENSG00000131323 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1383842739 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2753,RMVar_hsa_circ_169430,RMVar_hsa_circ_273169,RMVar_hsa_circ_309358,RMVar_hsa_circ_318210,RMVar_hsa_circ_169431,RMVar_hsa_circ_28884,RMVar_hsa_circ_297681,RMVar_hsa_circ_169429,RMVar_hsa_circ_297188,RMVar_hsa_circ_273716,RMVar_hsa_circ_169437,RMVar_hsa_circ_169438,RMVar_hsa_circ_169436,RMVar_hsa_circ_9633,RMVar_hsa_circ_169441,RMVar_hsa_circ_109812,RMVar_hsa_circ_325489,RMVar_hsa_circ_349615,RMVar_hsa_circ_301249,RMVar_hsa_circ_169442,RMVar_hsa_circ_169440 7203 RMVar_ID_7203 Human_SNP_ID_567950657 A-to-I Human chr14 + 102893133 102893133 102893133 CTTTGTGGCCGGGCATGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCTGAGGC CTTTGTGGCCGGGCATGGTGGCTCATGCCTGTGATCCCAGCACTTTGGGAGGCCGAGGCTGAGGC A G TRAF3 Ensembl:ENSG00000131323 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs758738651 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_169430,RMVar_hsa_circ_273169,RMVar_hsa_circ_309358,RMVar_hsa_circ_169429,RMVar_hsa_circ_297188,RMVar_hsa_circ_273716,RMVar_hsa_circ_169437,RMVar_hsa_circ_169438,RMVar_hsa_circ_57713,RMVar_hsa_circ_349615,RMVar_hsa_circ_301249,RMVar_hsa_circ_169440,RMVar_hsa_circ_270454,RMVar_hsa_circ_169444,RMVar_hsa_circ_169445,RMVar_hsa_circ_331318 7204 RMVar_ID_7204 Human_SNP_ID_567950700 A-to-I Human chr14 + 102893267 102893267 102893267 CAAAAATTACGCCAGCATAGTGGCAGGCGCCTATAGTCCCAGCTACTTGGGAGGCTGAGGCAGGA CAAAAATTACGCCAGCATAGTGGCAGGCGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGA A G TRAF3 Ensembl:ENSG00000131323 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1329390632 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_169430,RMVar_hsa_circ_273169,RMVar_hsa_circ_309358,RMVar_hsa_circ_169429,RMVar_hsa_circ_297188,RMVar_hsa_circ_273716,RMVar_hsa_circ_169437,RMVar_hsa_circ_169438,RMVar_hsa_circ_57713,RMVar_hsa_circ_349615,RMVar_hsa_circ_301249,RMVar_hsa_circ_169440,RMVar_hsa_circ_270454,RMVar_hsa_circ_169444,RMVar_hsa_circ_169445,RMVar_hsa_circ_331318 7205 RMVar_ID_7205 Human_SNP_ID_567951089 A-to-I Human chr14 + 102894954 102894954 102894954 AATTCCTTGGGCTCAAGTGGTCCGTCTGCCTCAGCCTTCCAAAGTGCTGAGACTACACGTATGAG AATTCCTTGGGCTCAAGTGGTCCGTCTGCCTCCGCCTTCCAAAGTGCTGAGACTACACGTATGAG A C TRAF3 Ensembl:ENSG00000131323 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1335690915 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_169430,RMVar_hsa_circ_273169,RMVar_hsa_circ_309358,RMVar_hsa_circ_169429,RMVar_hsa_circ_297188,RMVar_hsa_circ_273716,RMVar_hsa_circ_169437,RMVar_hsa_circ_169438,RMVar_hsa_circ_57713,RMVar_hsa_circ_349615,RMVar_hsa_circ_301249,RMVar_hsa_circ_169440,RMVar_hsa_circ_270454,RMVar_hsa_circ_169444,RMVar_hsa_circ_169445,RMVar_hsa_circ_331318 7206 RMVar_ID_7206 Human_SNP_ID_567966765 A-to-I Human chr14 - 102944289 102944289 102944289 AGGCTGCCAGCTCATGGCCACGGCCACACTCAAGAGGAACTCTGGCACCTGCCTGTTTGTGGCCG AGGCTGCCAGCTCATGGCCACGGCCACACTCAGGAGGAACTCTGGCACCTGCCTGTTTGTGGCCG T C CDC42BPB Ensembl:ENSG00000198752 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs768628164 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_40454,Human_RBP_ID_4282744,Human_RBP_ID_27429618 Human_miRNA_ID_2865904 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 7207 RMVar_ID_7207 Human_SNP_ID_567977548 A-to-I Human chr14 - 102979012 102979012 102979012 TTCCCAGATAAAGAACTTTGCTTATATTTTTTATTTTTTGAGACTGATCTCCTTCTGTCACCCAG TTCCCAGATAAAGAACTTTGCTTATATTTTTTGTTTTTTGAGACTGATCTCCTTCTGTCACCCAG T C CDC42BPB Ensembl:ENSG00000198752 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1440328318 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12278319 RMVar_hsa_circ_125390,RMVar_hsa_circ_169450,RMVar_hsa_circ_111755,RMVar_hsa_circ_169461,RMVar_hsa_circ_127645,RMVar_hsa_circ_169464,RMVar_hsa_circ_169470,RMVar_hsa_circ_91123,RMVar_hsa_circ_266038,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_169478,RMVar_hsa_circ_169479,RMVar_hsa_circ_120295,RMVar_hsa_circ_113125,RMVar_hsa_circ_346493,RMVar_hsa_circ_169481,RMVar_hsa_circ_169482,RMVar_hsa_circ_169484,RMVar_hsa_circ_56137,RMVar_hsa_circ_77559,RMVar_hsa_circ_169483,RMVar_hsa_circ_371750 7208 RMVar_ID_7208 Human_SNP_ID_567982047 A-to-I Human chr14 - 102995209 102995208 102995210 GATCGCGCCATTGCACTCCAGCCTGGAGAACAAGAGCGATACTCTGTCTCAAAAAAAAAAAAGAG GATCGCGCCATTGCACTCCAGCCTGGAGAAC__GAGCGATACTCTGTCTCAAAAAAAAAAAAGAG CTT C CDC42BPB Ensembl:ENSG00000198752 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1159501062 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_125390,RMVar_hsa_circ_169450,RMVar_hsa_circ_111755,RMVar_hsa_circ_169461,RMVar_hsa_circ_266038,RMVar_hsa_circ_110907,RMVar_hsa_circ_169479,RMVar_hsa_circ_120295,RMVar_hsa_circ_113125,RMVar_hsa_circ_169481,RMVar_hsa_circ_169482,RMVar_hsa_circ_26737,RMVar_hsa_circ_37679,RMVar_hsa_circ_56137,RMVar_hsa_circ_366743,RMVar_hsa_circ_33158,RMVar_hsa_circ_350938,RMVar_hsa_circ_169487,RMVar_hsa_circ_366763 7209 RMVar_ID_7209 Human_SNP_ID_567993791 A-to-I Human chr14 - 103037476 103037476 103037476 AAGCCTGAGCGACATAGCAAGGCCCCGATTCTACAAATTATACAAAAATTAGCTGGGCATGGTGG AAGCCTGAGCGACATAGCAAGGCCCCGATTCTCCAAATTATACAAAAATTAGCTGGGCATGGTGG T G CDC42BPB Ensembl:ENSG00000198752 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1254497203 Functional Loss SNV dbSNP153 33..33 33 - - - 7210 RMVar_ID_7210 Human_SNP_ID_567996501 A-to-I Human chr14 - 103047091 103047091 103047091 TCAGTAGAGATGGGATTTCACCATGTTGGCCAAGCTGTTCTCGAACTCCTTACCTCGTGATCCAC TCAGTAGAGATGGGATTTCACCATGTTGGCCAGGCTGTTCTCGAACTCCTTACCTCGTGATCCAC T C CDC42BPB Ensembl:ENSG00000198752 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941689745 Functional Loss SNV dbSNP153 33..33 33 - - - 7211 RMVar_ID_7211 Human_SNP_ID_568064925 A-to-I Human chr14 - 103298091 103298091 103298091 AAACTCCTGACCCCAAGTGATCCTCCCGCCTCAGCCTCCCGAGGTGCTGGGATTATAGGTGTGAG AAACTCCTGACCCCAAGTGATCCTCCCGCCTCGGCCTCCCGAGGTGCTGGGATTATAGGTGTGAG T C lnc-CKB-5,lnc-CKB-5:2 RNACentral:URS00008C398C,RNACentral:URS00009B5D73 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1309177199 Functional Loss SNV dbSNP153 33..33 33 - - - 7212 RMVar_ID_7212 Human_SNP_ID_568074631 A-to-I Human chr14 - 103332980 103332980 103332980 AGGAGAATCCTTGAACCCGGGAGGCACAGGTTACAGTGAGCCGAGATCACACCACTGCACTCCAG AGGAGAATCCTTGAACCCGGGAGGCACAGGTTGCAGTGAGCCGAGATCACACCACTGCACTCCAG T C LOC105370687-001 RNACentral:URS0000D77FE8 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1024585464 Functional Loss SNV dbSNP153 33..33 33 - - - 7213 RMVar_ID_7213 Human_SNP_ID_568074644 A-to-I Human chr14 - 103333006 103333006 103333006 ATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCCTTGAACCCGGGAGGCACAGGTTACAGTGA ATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAGTCCTTGAACCCGGGAGGCACAGGTTACAGTGA T C LOC105370687-001 RNACentral:URS0000D77FE8 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1356810464 Functional Loss SNV dbSNP153 33..33 33 - - - 7214 RMVar_ID_7214 Human_SNP_ID_568074661 A-to-I Human chr14 - 103333038 103333038 103333038 AAAAATTAGCTGGGCGTGGTGGCTCGCTTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAA AAAAATTAGCTGGGCGTGGTGGCTCGCTTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAA T C LOC105370687-001 RNACentral:URS0000D77FE8 lincRNA exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1230624161 Functional Loss SNV dbSNP153 33..33 33 - - - 7215 RMVar_ID_7215 Human_SNP_ID_568079488 A-to-I Human chr14 - 103344634 103344634 103344634 GCAAAATTGGGTGGAATTTCCCCTACTGCCCCAGCCAGGCATTGCTTCTGACTGCAGCATTAGGC GCAAAATTGGGTGGAATTTCCCCTACTGCCCCGGCCAGGCATTGCTTCTGACTGCAGCATTAGGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs371209434 Functional Loss SNV dbSNP153 33..33 33 - - - 7216 RMVar_ID_7216 Human_SNP_ID_568104449 A-to-I Human chr14 + 103432660 103432660 103432660 ATCACTCGAGCTCAGGAATTCGAGATCAGCCTAGGCAGCACAGAGAGACCCGTCTCTACCAAAAA ATCACTCGAGCTCAGGAATTCGAGATCAGCCTGGGCAGCACAGAGAGACCCGTCTCTACCAAAAA A G MARK3 Ensembl:ENSG00000075413 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1041698829 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_169502,RMVar_hsa_circ_169508,RMVar_hsa_circ_306212,RMVar_hsa_circ_109771,RMVar_hsa_circ_169507,RMVar_hsa_circ_169510,RMVar_hsa_circ_284483,RMVar_hsa_circ_328268,RMVar_hsa_circ_343824,RMVar_hsa_circ_312730,RMVar_hsa_circ_169511,RMVar_hsa_circ_169509 7217 RMVar_ID_7217 Human_SNP_ID_568105968 A-to-I Human chr14 + 103438797 103438793 103438797 AGGCAGATTGCTGAGCTCAGGAGTTCAAGACCAGCCTGGGCAACATGGCAAAACCCTGTCTCTAC AGGCAGATTGCTGAGCTCAGGAGTTCAAG____GCCTGGGCAACATGGCAAAACCCTGTCTCTAC GACCA G MARK3 Ensembl:ENSG00000075413 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs903185567 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_169502,RMVar_hsa_circ_169508,RMVar_hsa_circ_306212,RMVar_hsa_circ_109771,RMVar_hsa_circ_169507,RMVar_hsa_circ_169510,RMVar_hsa_circ_284483,RMVar_hsa_circ_328268,RMVar_hsa_circ_343824,RMVar_hsa_circ_312730,RMVar_hsa_circ_169511,RMVar_hsa_circ_169509 7218 RMVar_ID_7218 Human_SNP_ID_568106129 A-to-I Human chr14 + 103439488 103439488 103439488 TGGAGTGCAGTAGTGCGATCTCAGCTCACTGTAACCTCTGCCTCCCAAGTTCAAGCGATTCTTGT TGGAGTGCAGTAGTGCGATCTCAGCTCACTGTCACCTCTGCCTCCCAAGTTCAAGCGATTCTTGT A C MARK3 Ensembl:ENSG00000075413 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs745912774 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_169502,RMVar_hsa_circ_169508,RMVar_hsa_circ_306212,RMVar_hsa_circ_109771,RMVar_hsa_circ_169507,RMVar_hsa_circ_169510,RMVar_hsa_circ_284483,RMVar_hsa_circ_328268,RMVar_hsa_circ_343824,RMVar_hsa_circ_312730,RMVar_hsa_circ_169511,RMVar_hsa_circ_169509 7219 RMVar_ID_7219 Human_SNP_ID_568107153 A-to-I Human chr14 + 103443629 103443629 103443629 AGCGGTCACAGTGGAAGTCGTCTTTGAGACTTAGAGCGTTTGAGGAAGGGGTCGTCTTTAAAATA AGCGGTCACAGTGGAAGTCGTCTTTGAGACTTGGAGCGTTTGAGGAAGGGGTCGTCTTTAAAATA A G MARK3 Ensembl:ENSG00000075413 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs757657937 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12280644 RMVar_hsa_circ_169502,RMVar_hsa_circ_169508,RMVar_hsa_circ_306212,RMVar_hsa_circ_109771,RMVar_hsa_circ_169507,RMVar_hsa_circ_169510,RMVar_hsa_circ_284483,RMVar_hsa_circ_328268,RMVar_hsa_circ_343824,RMVar_hsa_circ_312730,RMVar_hsa_circ_169511,RMVar_hsa_circ_169509 7220 RMVar_ID_7220 Human_SNP_ID_568108048 A-to-I Human chr14 + 103447256 103447252 103447257 AGGAGGTCAAGGCTACAGTGAACTATGATCACACCACTGCACTTCAACCTGGGCAGCAGAGCGAG AGGAGGTCAAGGCTACAGTGAACTATGAT_____CACTGCACTTCAACCTGGGCAGCAGAGCGAG TCACAC T MARK3 Ensembl:ENSG00000075413 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1301250472 Functional Loss DEL dbSNP153 30..34 33 - - - Human_RBP_ID_22921377,Human_RBP_ID_25124740 RMVar_hsa_circ_169502,RMVar_hsa_circ_169508,RMVar_hsa_circ_306212,RMVar_hsa_circ_109771,RMVar_hsa_circ_169507,RMVar_hsa_circ_169510,RMVar_hsa_circ_284483,RMVar_hsa_circ_328268,RMVar_hsa_circ_343824,RMVar_hsa_circ_312730,RMVar_hsa_circ_169511,RMVar_hsa_circ_169509 7221 RMVar_ID_7221 Human_SNP_ID_568113906 A-to-I Human chr14 + 103468600 103468600 103468600 CACCTGCCTTGGCCTCCCAGAGCGCTGGAATTACAGGCATGAGCCACCGTGCCTGGCCAGCATTT CACCTGCCTTGGCCTCCCAGAGCGCTGGAATTTCAGGCATGAGCCACCGTGCCTGGCCAGCATTT A T MARK3 Ensembl:ENSG00000075413 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1457514475 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24402,RMVar_hsa_circ_169510,RMVar_hsa_circ_312730,RMVar_hsa_circ_169509,RMVar_hsa_circ_311738,RMVar_hsa_circ_323142,RMVar_hsa_circ_13215,RMVar_hsa_circ_169516,RMVar_hsa_circ_169517,RMVar_hsa_circ_306814,RMVar_hsa_circ_319704,RMVar_hsa_circ_95136,RMVar_hsa_circ_329672,RMVar_hsa_circ_169519,RMVar_hsa_circ_169520,RMVar_hsa_circ_169518,RMVar_hsa_circ_322538,RMVar_hsa_circ_169531,RMVar_hsa_circ_169528,RMVar_hsa_circ_169529,RMVar_hsa_circ_371310,RMVar_hsa_circ_80019,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_169539,RMVar_hsa_circ_169536,RMVar_hsa_circ_298998,RMVar_hsa_circ_363113,RMVar_hsa_circ_314223,RMVar_hsa_circ_169537,RMVar_hsa_circ_169538,RMVar_hsa_circ_327373,RMVar_hsa_circ_328498,RMVar_hsa_circ_370823 7222 RMVar_ID_7222 Human_SNP_ID_568115201 A-to-I Human chr14 + 103473074 103473074 103473074 AACTCAGATGGATCTCAAGGGAATTATACTGCATGAAAGTACACAAAAGGTTACATTCCATGGAT AACTCAGATGGATCTCAAGGGAATTATACTGCCTGAAAGTACACAAAAGGTTACATTCCATGGAT A C MARK3 Ensembl:ENSG00000075413 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs12434605 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24402,RMVar_hsa_circ_169510,RMVar_hsa_circ_312730,RMVar_hsa_circ_169509,RMVar_hsa_circ_311738,RMVar_hsa_circ_323142,RMVar_hsa_circ_13215,RMVar_hsa_circ_169516,RMVar_hsa_circ_169517,RMVar_hsa_circ_306814,RMVar_hsa_circ_319704,RMVar_hsa_circ_95136,RMVar_hsa_circ_329672,RMVar_hsa_circ_169519,RMVar_hsa_circ_169520,RMVar_hsa_circ_169518,RMVar_hsa_circ_322538,RMVar_hsa_circ_169531,RMVar_hsa_circ_169528,RMVar_hsa_circ_169529,RMVar_hsa_circ_371310,RMVar_hsa_circ_80019,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_169539,RMVar_hsa_circ_169536,RMVar_hsa_circ_298998,RMVar_hsa_circ_363113,RMVar_hsa_circ_314223,RMVar_hsa_circ_169537,RMVar_hsa_circ_169538,RMVar_hsa_circ_327373,RMVar_hsa_circ_328498,RMVar_hsa_circ_370823 7223 RMVar_ID_7223 Human_SNP_ID_568115202 A-to-I Human chr14 + 103473074 103473074 103473074 AACTCAGATGGATCTCAAGGGAATTATACTGCATGAAAGTACACAAAAGGTTACATTCCATGGAT AACTCAGATGGATCTCAAGGGAATTATACTGCGTGAAAGTACACAAAAGGTTACATTCCATGGAT A G MARK3 Ensembl:ENSG00000075413 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs12434605 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24402,RMVar_hsa_circ_169510,RMVar_hsa_circ_312730,RMVar_hsa_circ_169509,RMVar_hsa_circ_311738,RMVar_hsa_circ_323142,RMVar_hsa_circ_13215,RMVar_hsa_circ_169516,RMVar_hsa_circ_169517,RMVar_hsa_circ_306814,RMVar_hsa_circ_319704,RMVar_hsa_circ_95136,RMVar_hsa_circ_329672,RMVar_hsa_circ_169519,RMVar_hsa_circ_169520,RMVar_hsa_circ_169518,RMVar_hsa_circ_322538,RMVar_hsa_circ_169531,RMVar_hsa_circ_169528,RMVar_hsa_circ_169529,RMVar_hsa_circ_371310,RMVar_hsa_circ_80019,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_169539,RMVar_hsa_circ_169536,RMVar_hsa_circ_298998,RMVar_hsa_circ_363113,RMVar_hsa_circ_314223,RMVar_hsa_circ_169537,RMVar_hsa_circ_169538,RMVar_hsa_circ_327373,RMVar_hsa_circ_328498,RMVar_hsa_circ_370823 7224 RMVar_ID_7224 Human_SNP_ID_568115203 A-to-I Human chr14 + 103473074 103473074 103473074 AACTCAGATGGATCTCAAGGGAATTATACTGCATGAAAGTACACAAAAGGTTACATTCCATGGAT AACTCAGATGGATCTCAAGGGAATTATACTGCTTGAAAGTACACAAAAGGTTACATTCCATGGAT A T MARK3 Ensembl:ENSG00000075413 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs12434605 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24402,RMVar_hsa_circ_169510,RMVar_hsa_circ_312730,RMVar_hsa_circ_169509,RMVar_hsa_circ_311738,RMVar_hsa_circ_323142,RMVar_hsa_circ_13215,RMVar_hsa_circ_169516,RMVar_hsa_circ_169517,RMVar_hsa_circ_306814,RMVar_hsa_circ_319704,RMVar_hsa_circ_95136,RMVar_hsa_circ_329672,RMVar_hsa_circ_169519,RMVar_hsa_circ_169520,RMVar_hsa_circ_169518,RMVar_hsa_circ_322538,RMVar_hsa_circ_169531,RMVar_hsa_circ_169528,RMVar_hsa_circ_169529,RMVar_hsa_circ_371310,RMVar_hsa_circ_80019,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_169539,RMVar_hsa_circ_169536,RMVar_hsa_circ_298998,RMVar_hsa_circ_363113,RMVar_hsa_circ_314223,RMVar_hsa_circ_169537,RMVar_hsa_circ_169538,RMVar_hsa_circ_327373,RMVar_hsa_circ_328498,RMVar_hsa_circ_370823 7225 RMVar_ID_7225 Human_SNP_ID_568116834 A-to-I Human chr14 + 103479074 103479074 103479074 AGACGGTCTCACTCTGTCACCTAGGCTAAAGTACAATGGTGCAAACACGGCTCATTGCAACTTCG AGACGGTCTCACTCTGTCACCTAGGCTAAAGTGCAATGGTGCAAACACGGCTCATTGCAACTTCG A G MARK3 Ensembl:ENSG00000075413 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs538013875 Functional Loss SNV dbSNP153 33..33 33 - - - 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 7226 RMVar_ID_7226 Human_SNP_ID_568117008 A-to-I Human chr14 + 103479726 103479726 103479726 GCGATCTCAGCTCACCGCAACCTCTACCTCCCAGGTTTAAGTGATTCTCCTACCTCAGCCTCCTG GCGATCTCAGCTCACCGCAACCTCTACCTCCCGGGTTTAAGTGATTCTCCTACCTCAGCCTCCTG A G MARK3 Ensembl:ENSG00000075413 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1467599585 Functional Loss SNV dbSNP153 33..33 33 - - - 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 7227 RMVar_ID_7227 Human_SNP_ID_568117759 A-to-I Human chr14 + 103482432 103482432 103482432 AGTCCCAGCTACCAGGGAGACTGAGGCAGGAGAATTACTTGAACCCAGGAGGCAGAGTTTGCAGT AGTCCCAGCTACCAGGGAGACTGAGGCAGGAGCATTACTTGAACCCAGGAGGCAGAGTTTGCAGT A C MARK3 Ensembl:ENSG00000075413 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs535943476 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_169509,RMVar_hsa_circ_323142,RMVar_hsa_circ_169517,RMVar_hsa_circ_95136,RMVar_hsa_circ_169518,RMVar_hsa_circ_46555,RMVar_hsa_circ_169535,RMVar_hsa_circ_325968,RMVar_hsa_circ_363113,RMVar_hsa_circ_169537,RMVar_hsa_circ_169538,RMVar_hsa_circ_327373,RMVar_hsa_circ_328498,RMVar_hsa_circ_307718 7228 RMVar_ID_7228 Human_SNP_ID_568117760 A-to-I Human chr14 + 103482432 103482432 103482432 AGTCCCAGCTACCAGGGAGACTGAGGCAGGAGAATTACTTGAACCCAGGAGGCAGAGTTTGCAGT AGTCCCAGCTACCAGGGAGACTGAGGCAGGAGGATTACTTGAACCCAGGAGGCAGAGTTTGCAGT A G MARK3 Ensembl:ENSG00000075413 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs535943476 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_169509,RMVar_hsa_circ_323142,RMVar_hsa_circ_169517,RMVar_hsa_circ_95136,RMVar_hsa_circ_169518,RMVar_hsa_circ_46555,RMVar_hsa_circ_169535,RMVar_hsa_circ_325968,RMVar_hsa_circ_363113,RMVar_hsa_circ_169537,RMVar_hsa_circ_169538,RMVar_hsa_circ_327373,RMVar_hsa_circ_328498,RMVar_hsa_circ_307718 7229 RMVar_ID_7229 Human_SNP_ID_568118213 A-to-I Human chr14 + 103484226 103484226 103484226 CTGCGATGGAGTCTCGCTCTTTTACCCAGGCTAGAGTGCAATGGCACGATCTCGGGTCACTGCAA CTGCGATGGAGTCTCGCTCTTTTACCCAGGCTGGAGTGCAATGGCACGATCTCGGGTCACTGCAA A G MARK3 Ensembl:ENSG00000075413 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1362733981 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_169509,RMVar_hsa_circ_323142,RMVar_hsa_circ_169517,RMVar_hsa_circ_95136,RMVar_hsa_circ_169518,RMVar_hsa_circ_46555,RMVar_hsa_circ_169535,RMVar_hsa_circ_325968,RMVar_hsa_circ_363113,RMVar_hsa_circ_169537,RMVar_hsa_circ_169538,RMVar_hsa_circ_327373,RMVar_hsa_circ_328498,RMVar_hsa_circ_307718 7230 RMVar_ID_7230 Human_SNP_ID_568118220 A-to-I Human chr14 + 103484252 103484252 103484252 CAGGCTAGAGTGCAATGGCACGATCTCGGGTCACTGCAACCTCCATCTCCCGGGTTCATGCAGTT CAGGCTAGAGTGCAATGGCACGATCTCGGGTCGCTGCAACCTCCATCTCCCGGGTTCATGCAGTT A G MARK3 Ensembl:ENSG00000075413 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs982847567 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_169509,RMVar_hsa_circ_323142,RMVar_hsa_circ_169517,RMVar_hsa_circ_95136,RMVar_hsa_circ_169518,RMVar_hsa_circ_46555,RMVar_hsa_circ_169535,RMVar_hsa_circ_325968,RMVar_hsa_circ_363113,RMVar_hsa_circ_169537,RMVar_hsa_circ_169538,RMVar_hsa_circ_327373,RMVar_hsa_circ_328498,RMVar_hsa_circ_307718 7231 RMVar_ID_7231 Human_SNP_ID_568118242 A-to-I Human chr14 + 103484326 103484326 103484326 CAGCCTCCCAGTAGCTGGGATTACAGGCACACACCACCACACCTGGCTGATTTTTGTATTTTTAA CAGCCTCCCAGTAGCTGGGATTACAGGCACACGCCACCACACCTGGCTGATTTTTGTATTTTTAA A G MARK3 Ensembl:ENSG00000075413 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1555401447 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_169509,RMVar_hsa_circ_323142,RMVar_hsa_circ_169517,RMVar_hsa_circ_95136,RMVar_hsa_circ_169518,RMVar_hsa_circ_46555,RMVar_hsa_circ_169535,RMVar_hsa_circ_325968,RMVar_hsa_circ_363113,RMVar_hsa_circ_169537,RMVar_hsa_circ_169538,RMVar_hsa_circ_327373,RMVar_hsa_circ_328498,RMVar_hsa_circ_307718 7232 RMVar_ID_7232 Human_SNP_ID_568118561 A-to-I Human chr14 + 103485373 103485373 103485373 ATAGTGTACTGTAGCCTTGAACTCCTGGGCTCAAATGATCCTCCTGTGTTGGCTTCTTGAGTAGC ATAGTGTACTGTAGCCTTGAACTCCTGGGCTCCAATGATCCTCCTGTGTTGGCTTCTTGAGTAGC A C MARK3 Ensembl:ENSG00000075413 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs949466261 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12281560 RMVar_hsa_circ_169509,RMVar_hsa_circ_323142,RMVar_hsa_circ_169517,RMVar_hsa_circ_95136,RMVar_hsa_circ_169518,RMVar_hsa_circ_46555,RMVar_hsa_circ_169535,RMVar_hsa_circ_325968,RMVar_hsa_circ_363113,RMVar_hsa_circ_169537,RMVar_hsa_circ_169538,RMVar_hsa_circ_327373,RMVar_hsa_circ_328498,RMVar_hsa_circ_307718 7233 RMVar_ID_7233 Human_SNP_ID_568118578 A-to-I Human chr14 + 103485463 103485463 103485463 ACCTGGCTAATTTTTTATTTTTTGTAGAGATGAAGTCTTCCCATGTTACCCAGGCTGGTCTCAAA ACCTGGCTAATTTTTTATTTTTTGTAGAGATGCAGTCTTCCCATGTTACCCAGGCTGGTCTCAAA A C MARK3 Ensembl:ENSG00000075413 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1326601458 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17562759 RMVar_hsa_circ_169509,RMVar_hsa_circ_323142,RMVar_hsa_circ_169517,RMVar_hsa_circ_95136,RMVar_hsa_circ_169518,RMVar_hsa_circ_46555,RMVar_hsa_circ_169535,RMVar_hsa_circ_325968,RMVar_hsa_circ_363113,RMVar_hsa_circ_169537,RMVar_hsa_circ_169538,RMVar_hsa_circ_327373,RMVar_hsa_circ_328498,RMVar_hsa_circ_307718 7234 RMVar_ID_7234 Human_SNP_ID_568118594 A-to-I Human chr14 + 103485541 103485541 103485541 GGGATCCTCCAGTCTCAGCCTTCCAAAACACTAGGTTTACAGGCATGAGCCACCATGCCTGTCCT GGGATCCTCCAGTCTCAGCCTTCCAAAACACTGGGTTTACAGGCATGAGCCACCATGCCTGTCCT A G MARK3 Ensembl:ENSG00000075413 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs184700106 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1171121,Human_RBP_ID_12281565,Human_RBP_ID_23306684 RMVar_hsa_circ_169509,RMVar_hsa_circ_323142,RMVar_hsa_circ_169517,RMVar_hsa_circ_95136,RMVar_hsa_circ_169518,RMVar_hsa_circ_46555,RMVar_hsa_circ_169535,RMVar_hsa_circ_325968,RMVar_hsa_circ_363113,RMVar_hsa_circ_169537,RMVar_hsa_circ_169538,RMVar_hsa_circ_327373,RMVar_hsa_circ_328498,RMVar_hsa_circ_307718 7235 RMVar_ID_7235 Human_SNP_ID_568118787 A-to-I Human chr14 + 103486328 103486328 103486328 AGGTGTGGTGGTACATGCCGGTAGTCCCAGCTATTTGGGAGGCTGAGGCAGGAGGATGGTTTGAG AGGTGTGGTGGTACATGCCGGTAGTCCCAGCTCTTTGGGAGGCTGAGGCAGGAGGATGGTTTGAG A C MARK3 Ensembl:ENSG00000075413 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1390712688 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_169509,RMVar_hsa_circ_323142,RMVar_hsa_circ_169517,RMVar_hsa_circ_95136,RMVar_hsa_circ_169518,RMVar_hsa_circ_46555,RMVar_hsa_circ_169535,RMVar_hsa_circ_325968,RMVar_hsa_circ_363113,RMVar_hsa_circ_169537,RMVar_hsa_circ_169538,RMVar_hsa_circ_327373,RMVar_hsa_circ_328498,RMVar_hsa_circ_307718 7236 RMVar_ID_7236 Human_SNP_ID_568118788 A-to-I Human chr14 + 103486328 103486328 103486328 AGGTGTGGTGGTACATGCCGGTAGTCCCAGCTATTTGGGAGGCTGAGGCAGGAGGATGGTTTGAG AGGTGTGGTGGTACATGCCGGTAGTCCCAGCTGTTTGGGAGGCTGAGGCAGGAGGATGGTTTGAG A G MARK3 Ensembl:ENSG00000075413 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1390712688 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_169509,RMVar_hsa_circ_323142,RMVar_hsa_circ_169517,RMVar_hsa_circ_95136,RMVar_hsa_circ_169518,RMVar_hsa_circ_46555,RMVar_hsa_circ_169535,RMVar_hsa_circ_325968,RMVar_hsa_circ_363113,RMVar_hsa_circ_169537,RMVar_hsa_circ_169538,RMVar_hsa_circ_327373,RMVar_hsa_circ_328498,RMVar_hsa_circ_307718 7237 RMVar_ID_7237 Human_SNP_ID_568118800 A-to-I Human chr14 + 103486396 103486396 103486396 GGGAGATGGAGGTTGTAGTGAGCCGAGATCACACCATTGTATTCCAGCCTGGACGGTAGAGCCAG GGGAGATGGAGGTTGTAGTGAGCCGAGATCACGCCATTGTATTCCAGCCTGGACGGTAGAGCCAG A G MARK3 Ensembl:ENSG00000075413 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 29129909,30559470 RNA-Seq:(High) rs1054078513 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6327418,Human_RBP_ID_12281597 RMVar_hsa_circ_169509,RMVar_hsa_circ_323142,RMVar_hsa_circ_169517,RMVar_hsa_circ_95136,RMVar_hsa_circ_169518,RMVar_hsa_circ_46555,RMVar_hsa_circ_169535,RMVar_hsa_circ_325968,RMVar_hsa_circ_363113,RMVar_hsa_circ_169537,RMVar_hsa_circ_169538,RMVar_hsa_circ_327373,RMVar_hsa_circ_328498,RMVar_hsa_circ_307718 7238 RMVar_ID_7238 Human_SNP_ID_568118974 A-to-I Human chr14 + 103487050 103487050 103487050 ACGATTCTTATACCTCAGCCTCCTGAGTAGCTAGGATTACAGGGGCCCGCCACCACACCCAACTA ACGATTCTTATACCTCAGCCTCCTGAGTAGCTGGGATTACAGGGGCCCGCCACCACACCCAACTA A G MARK3 Ensembl:ENSG00000075413 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1170563882 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_169509,RMVar_hsa_circ_323142,RMVar_hsa_circ_169517,RMVar_hsa_circ_95136,RMVar_hsa_circ_169518,RMVar_hsa_circ_46555,RMVar_hsa_circ_169535,RMVar_hsa_circ_325968,RMVar_hsa_circ_363113,RMVar_hsa_circ_169537,RMVar_hsa_circ_169538,RMVar_hsa_circ_327373,RMVar_hsa_circ_328498,RMVar_hsa_circ_307718 7239 RMVar_ID_7239 Human_SNP_ID_568119199 A-to-I Human chr14 + 103487933 103487933 103487933 AGCCGGGCGTGGTGGTGGGTGCCTGTAGTCCCAGCTACTTGGGAGACTGAGGCAGGAGAATGGCG AGCCGGGCGTGGTGGTGGGTGCCTGTAGTCCCGGCTACTTGGGAGACTGAGGCAGGAGAATGGCG A G MARK3 Ensembl:ENSG00000075413 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs547442949 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_169509,RMVar_hsa_circ_323142,RMVar_hsa_circ_169517,RMVar_hsa_circ_95136,RMVar_hsa_circ_169518,RMVar_hsa_circ_46555,RMVar_hsa_circ_169535,RMVar_hsa_circ_325968,RMVar_hsa_circ_363113,RMVar_hsa_circ_169537,RMVar_hsa_circ_169538,RMVar_hsa_circ_327373,RMVar_hsa_circ_328498,RMVar_hsa_circ_307718 7240 RMVar_ID_7240 Human_SNP_ID_568119317 A-to-I Human chr14 + 103488390 103488390 103488390 TGGTCTCCTTGATCTGTGTGGGGCCTAGAGTTACTTCCACCACAGCAAAATCTCATTATTGTTGC TGGTCTCCTTGATCTGTGTGGGGCCTAGAGTTGCTTCCACCACAGCAAAATCTCATTATTGTTGC A G MARK3 Ensembl:ENSG00000075413 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7146717 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_169509,RMVar_hsa_circ_323142,RMVar_hsa_circ_169517,RMVar_hsa_circ_95136,RMVar_hsa_circ_169518,RMVar_hsa_circ_46555,RMVar_hsa_circ_169535,RMVar_hsa_circ_325968,RMVar_hsa_circ_363113,RMVar_hsa_circ_169537,RMVar_hsa_circ_169538,RMVar_hsa_circ_327373,RMVar_hsa_circ_328498,RMVar_hsa_circ_307718 7241 RMVar_ID_7241 Human_SNP_ID_568119318 A-to-I Human chr14 + 103488390 103488390 103488390 TGGTCTCCTTGATCTGTGTGGGGCCTAGAGTTACTTCCACCACAGCAAAATCTCATTATTGTTGC TGGTCTCCTTGATCTGTGTGGGGCCTAGAGTTTCTTCCACCACAGCAAAATCTCATTATTGTTGC A T MARK3 Ensembl:ENSG00000075413 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7146717 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_169509,RMVar_hsa_circ_323142,RMVar_hsa_circ_169517,RMVar_hsa_circ_95136,RMVar_hsa_circ_169518,RMVar_hsa_circ_46555,RMVar_hsa_circ_169535,RMVar_hsa_circ_325968,RMVar_hsa_circ_363113,RMVar_hsa_circ_169537,RMVar_hsa_circ_169538,RMVar_hsa_circ_327373,RMVar_hsa_circ_328498,RMVar_hsa_circ_307718 7242 RMVar_ID_7242 Human_SNP_ID_568119476 A-to-I Human chr14 + 103489158 103489158 103489158 TCAGAGGGAAAATGGATCAGATAACACTTCATAGAGATGACGACATCTGGTTCATTTTTGAAGAG TCAGAGGGAAAATGGATCAGATAACACTTCATGGAGATGACGACATCTGGTTCATTTTTGAAGAG A G MARK3 Ensembl:ENSG00000075413 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs911556 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_169509,RMVar_hsa_circ_323142,RMVar_hsa_circ_169517,RMVar_hsa_circ_95136,RMVar_hsa_circ_169518,RMVar_hsa_circ_46555,RMVar_hsa_circ_169535,RMVar_hsa_circ_325968,RMVar_hsa_circ_363113,RMVar_hsa_circ_169537,RMVar_hsa_circ_169538,RMVar_hsa_circ_327373,RMVar_hsa_circ_328498,RMVar_hsa_circ_307718 7243 RMVar_ID_7243 Human_SNP_ID_568119477 A-to-I Human chr14 + 103489158 103489158 103489158 TCAGAGGGAAAATGGATCAGATAACACTTCATAGAGATGACGACATCTGGTTCATTTTTGAAGAG TCAGAGGGAAAATGGATCAGATAACACTTCATTGAGATGACGACATCTGGTTCATTTTTGAAGAG A T MARK3 Ensembl:ENSG00000075413 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs911556 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_169509,RMVar_hsa_circ_323142,RMVar_hsa_circ_169517,RMVar_hsa_circ_95136,RMVar_hsa_circ_169518,RMVar_hsa_circ_46555,RMVar_hsa_circ_169535,RMVar_hsa_circ_325968,RMVar_hsa_circ_363113,RMVar_hsa_circ_169537,RMVar_hsa_circ_169538,RMVar_hsa_circ_327373,RMVar_hsa_circ_328498,RMVar_hsa_circ_307718 7244 RMVar_ID_7244 Human_SNP_ID_568120594 A-to-I Human chr14 + 103493396 103493396 103493396 ACATCCATTAGCATTAACTAGAAGTCAGACGCATCAGAAGGTTTCTATTTACCCTCTTACTCACT ACATCCATTAGCATTAACTAGAAGTCAGACGCCTCAGAAGGTTTCTATTTACCCTCTTACTCACT A C MARK3 Ensembl:ENSG00000075413 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2756137 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95136,RMVar_hsa_circ_169518,RMVar_hsa_circ_291516,RMVar_hsa_circ_169543 7245 RMVar_ID_7245 Human_SNP_ID_568120595 A-to-I Human chr14 + 103493396 103493396 103493396 ACATCCATTAGCATTAACTAGAAGTCAGACGCATCAGAAGGTTTCTATTTACCCTCTTACTCACT ACATCCATTAGCATTAACTAGAAGTCAGACGCGTCAGAAGGTTTCTATTTACCCTCTTACTCACT A G MARK3 Ensembl:ENSG00000075413 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2756137 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95136,RMVar_hsa_circ_169518,RMVar_hsa_circ_291516,RMVar_hsa_circ_169543 7246 RMVar_ID_7246 Human_SNP_ID_568120811 A-to-I Human chr14 + 103494069 103494069 103494069 AGGCCTGGCCAACATGGCAAAACCCCATCTCTACTAAAAATACAAAAATTAGCCAGGGGTGGTGG AGGCCTGGCCAACATGGCAAAACCCCATCTCTTCTAAAAATACAAAAATTAGCCAGGGGTGGTGG A T MARK3 Ensembl:ENSG00000075413 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1352084951 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95136,RMVar_hsa_circ_169518,RMVar_hsa_circ_291516,RMVar_hsa_circ_169543 7247 RMVar_ID_7247 Human_SNP_ID_568121242 A-to-I Human chr14 + 103495429 103495429 103495429 TTGAACCCAGGAGGCGTAGGTTGCAGAGAGCCAAGATCACACCATTGCACTCCAGCCTGGCGACA TTGAACCCAGGAGGCGTAGGTTGCAGAGAGCCGAGATCACACCATTGCACTCCAGCCTGGCGACA A G MARK3 Ensembl:ENSG00000075413 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs527808940 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95136,RMVar_hsa_circ_169518,RMVar_hsa_circ_291516,RMVar_hsa_circ_169543 7248 RMVar_ID_7248 Human_SNP_ID_568121465 A-to-I Human chr14 + 103496317 103496317 103496317 GAAGATTAGGAAATGTCCAGGCACCATGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCTGAG GAAGATTAGGAAATGTCCAGGCACCATGGCTCGTGCCTATAATCCCAGCACTTTGGGAGGCTGAG A G MARK3 Ensembl:ENSG00000075413 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1276122496 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95136,RMVar_hsa_circ_169518,RMVar_hsa_circ_291516,RMVar_hsa_circ_169543 7249 RMVar_ID_7249 Human_SNP_ID_568121832 A-to-I Human chr14 + 103498046 103498046 103498046 CGAGACTAGACTGGCCAACATGGCAAAACCCTATCTCTACTGAAAATATAGAAATTAACTGGGCA CGAGACTAGACTGGCCAACATGGCAAAACCCTCTCTCTACTGAAAATATAGAAATTAACTGGGCA A C MARK3 Ensembl:ENSG00000075413 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs549562204 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95136,RMVar_hsa_circ_169518,RMVar_hsa_circ_291516,RMVar_hsa_circ_169543 7250 RMVar_ID_7250 Human_SNP_ID_568121833 A-to-I Human chr14 + 103498046 103498046 103498046 CGAGACTAGACTGGCCAACATGGCAAAACCCTATCTCTACTGAAAATATAGAAATTAACTGGGCA CGAGACTAGACTGGCCAACATGGCAAAACCCTGTCTCTACTGAAAATATAGAAATTAACTGGGCA A G MARK3 Ensembl:ENSG00000075413 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs549562204 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95136,RMVar_hsa_circ_169518,RMVar_hsa_circ_291516,RMVar_hsa_circ_169543 7251 RMVar_ID_7251 Human_SNP_ID_568139161 A-to-I Human chr14 - 103557829 103557829 103557829 GGCACCATGCCTGGCTAATTTTTGTATTTTTAATAGAGTTGAGATTTCACCATGATGGTCAGGCT GGCACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGTTGAGATTTCACCATGATGGTCAGGCT T C BAG5 Ensembl:ENSG00000166170 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1313747340 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4283317,Human_RBP_ID_6327895,Human_RBP_ID_12282726 7252 RMVar_ID_7252 Human_SNP_ID_568141327 A-to-I Human chr14 + 103563895 103563890 103563896 GTTAATTAAAAATTGGACGGGCTCCGTGGCTCACGCTTGTAATCCCAGCACTTTGGGAGGCCGAG GTTAATTAAAAATTGGACGGGCTCCGTG______GCTTGTAATCCCAGCACTTTGGGAGGCCGAG GGCTCAC G COA8,AL139300.1,KLC1 Ensembl:ENSG00000256053,Ensembl:ENSG00000256500,Ensembl:ENSG00000126214 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1044154788 Functional Loss DEL dbSNP153 29..34 33 - - - RMVar_hsa_circ_34025 7253 RMVar_ID_7253 Human_SNP_ID_568145611 A-to-I Human chr14 + 103579834 103579834 103579834 AAGACACAAAACTTAGCTGGACGTGGTGGCGTATGCCTGTAATCCCAGCTACTTGGGAGGCTGAG AAGACACAAAACTTAGCTGGACGTGGTGGCGTGTGCCTGTAATCCCAGCTACTTGGGAGGCTGAG A G COA8,AL139300.1,KLC1 Ensembl:ENSG00000256053,Ensembl:ENSG00000256500,Ensembl:ENSG00000126214 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1286997036 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11437,RMVar_hsa_circ_169555,RMVar_hsa_circ_169557,RMVar_hsa_circ_280815,RMVar_hsa_circ_47020,RMVar_hsa_circ_169556,RMVar_hsa_circ_124329,RMVar_hsa_circ_169558,RMVar_hsa_circ_169559,RMVar_hsa_circ_169560 7254 RMVar_ID_7254 Human_SNP_ID_568145612 A-to-I Human chr14 + 103579834 103579834 103579834 AAGACACAAAACTTAGCTGGACGTGGTGGCGTATGCCTGTAATCCCAGCTACTTGGGAGGCTGAG AAGACACAAAACTTAGCTGGACGTGGTGGCGTTTGCCTGTAATCCCAGCTACTTGGGAGGCTGAG A T COA8,AL139300.1,KLC1 Ensembl:ENSG00000256053,Ensembl:ENSG00000256500,Ensembl:ENSG00000126214 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1286997036 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11437,RMVar_hsa_circ_169555,RMVar_hsa_circ_169557,RMVar_hsa_circ_280815,RMVar_hsa_circ_47020,RMVar_hsa_circ_169556,RMVar_hsa_circ_124329,RMVar_hsa_circ_169558,RMVar_hsa_circ_169559,RMVar_hsa_circ_169560 7255 RMVar_ID_7255 Human_SNP_ID_568147195 A-to-I Human chr14 + 103585741 103585741 103585741 GGGACTACAGACGCACGCCACTACACCCGGCTAATTTTTGTACTTTTAGTAGAGACGGGGTTTCA GGGACTACAGACGCACGCCACTACACCCGGCTCATTTTTGTACTTTTAGTAGAGACGGGGTTTCA A C COA8,AL139300.1,KLC1 Ensembl:ENSG00000256053,Ensembl:ENSG00000256500,Ensembl:ENSG00000126214 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1369799679 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11437,RMVar_hsa_circ_169555,RMVar_hsa_circ_169557,RMVar_hsa_circ_280815,RMVar_hsa_circ_169556,RMVar_hsa_circ_124329,RMVar_hsa_circ_169558,RMVar_hsa_circ_169559,RMVar_hsa_circ_169560 7256 RMVar_ID_7256 Human_SNP_ID_568148689 A-to-I Human chr14 + 103590739 103590739 103590739 AAAATTAGCTGGGTGTGGTGGCACGCACCTGTAATCCCAGCTGCTCTGGAGGCTGAGGCATGCGA AAAATTAGCTGGGTGTGGTGGCACGCACCTGTGATCCCAGCTGCTCTGGAGGCTGAGGCATGCGA A G COA8,AL139300.1,KLC1 Ensembl:ENSG00000256053,Ensembl:ENSG00000256500,Ensembl:ENSG00000126214 Protein coding,Protein coding,Protein coding 3'UTR,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1351999556 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2252705,Human_miRNA_ID_2825475,Human_miRNA_ID_2859446,Human_miRNA_ID_2890729 RMVar_hsa_circ_169557,RMVar_hsa_circ_124329,RMVar_hsa_circ_169561,RMVar_hsa_circ_169560 7257 RMVar_ID_7257 Human_SNP_ID_568148701 A-to-I Human chr14 + 103590778 103590778 103590778 GCTGCTCTGGAGGCTGAGGCATGCGACGCTTGAACCCAGGAGGCGGAGGTTGCAGTGATCCAAGA GCTGCTCTGGAGGCTGAGGCATGCGACGCTTGCACCCAGGAGGCGGAGGTTGCAGTGATCCAAGA A C COA8,AL139300.1,KLC1 Ensembl:ENSG00000256053,Ensembl:ENSG00000256500,Ensembl:ENSG00000126214 Protein coding,Protein coding,Protein coding 3'UTR,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1329134737 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1815442 Human_miRNA_ID_2742844 RMVar_hsa_circ_169557,RMVar_hsa_circ_124329,RMVar_hsa_circ_169561,RMVar_hsa_circ_169560 7258 RMVar_ID_7258 Human_SNP_ID_568151923 A-to-I Human chr14 + 103602792 103602792 103602792 TAAAAACAAAAATCGGCTGGGCATGCTGAGGTAAGAGAATCGACTGAACCCAGGAGGCAGAGATT TAAAAACAAAAATCGGCTGGGCATGCTGAGGTGAGAGAATCGACTGAACCCAGGAGGCAGAGATT A G COA8,AL139300.1,KLC1 Ensembl:ENSG00000256053,Ensembl:ENSG00000256500,Ensembl:ENSG00000126214 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1055705244 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124329,RMVar_hsa_circ_169560 7259 RMVar_ID_7259 Human_SNP_ID_568161652 A-to-I Human chr14 + 103637905 103637905 103637905 TAGAGACAGGGTTTCATGGCATTGCCCTGGCTAGTCTTTAACTTCTGGGCTCAAATGATCTGCTC TAGAGACAGGGTTTCATGGCATTGCCCTGGCTGGTCTTTAACTTCTGGGCTCAAATGATCTGCTC A G AL139300.1,KLC1 Ensembl:ENSG00000256500,Ensembl:ENSG00000126214 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417628703 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124329,RMVar_hsa_circ_169560,RMVar_hsa_circ_169563,RMVar_hsa_circ_95264 7260 RMVar_ID_7260 Human_SNP_ID_568166524 A-to-I Human chr14 + 103655403 103655403 103655403 CGGCTCACTGCATCCTCTGCCTCCTGGGCTCAAATGATTCTCCTGCCTCAGCCTCCCAAGTAGCT CGGCTCACTGCATCCTCTGCCTCCTGGGCTCAGATGATTCTCCTGCCTCAGCCTCCCAAGTAGCT A G AL139300.1,KLC1 Ensembl:ENSG00000256500,Ensembl:ENSG00000126214 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1366806883 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124329,RMVar_hsa_circ_16874,RMVar_hsa_circ_169560,RMVar_hsa_circ_315490,RMVar_hsa_circ_169563,RMVar_hsa_circ_95264,RMVar_hsa_circ_353885,RMVar_hsa_circ_363394,RMVar_hsa_circ_53862,RMVar_hsa_circ_53212,RMVar_hsa_circ_169565,RMVar_hsa_circ_169566 7261 RMVar_ID_7261 Human_SNP_ID_568167544 A-to-I Human chr14 + 103659077 103659077 103659077 TTGGCTCACTGCAGCCTCCACCTCCTGGGTTCAAGCGATTCTCCCTTCTCAGCCTTCCAAGTAGC TTGGCTCACTGCAGCCTCCACCTCCTGGGTTCGAGCGATTCTCCCTTCTCAGCCTTCCAAGTAGC A G AL139300.1,KLC1 Ensembl:ENSG00000256500,Ensembl:ENSG00000126214 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1379920298 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124329,RMVar_hsa_circ_16874,RMVar_hsa_circ_169560,RMVar_hsa_circ_315490,RMVar_hsa_circ_169563,RMVar_hsa_circ_95264,RMVar_hsa_circ_363394,RMVar_hsa_circ_53862,RMVar_hsa_circ_53212,RMVar_hsa_circ_169566 7262 RMVar_ID_7262 Human_SNP_ID_568167923 A-to-I Human chr14 + 103660574 103660574 103660574 ATTTTGGGAGGCTGAAGCGGGTGGATTACCTGAGGCCAGGAGTTCAAGACCAGCCTGGCCAACAT ATTTTGGGAGGCTGAAGCGGGTGGATTACCTGGGGCCAGGAGTTCAAGACCAGCCTGGCCAACAT A G AL139300.1,KLC1 Ensembl:ENSG00000256500,Ensembl:ENSG00000126214 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1372596702 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124329,RMVar_hsa_circ_16874,RMVar_hsa_circ_169560,RMVar_hsa_circ_315490,RMVar_hsa_circ_169563,RMVar_hsa_circ_95264,RMVar_hsa_circ_363394,RMVar_hsa_circ_53862,RMVar_hsa_circ_53212,RMVar_hsa_circ_169566 7263 RMVar_ID_7263 Human_SNP_ID_568170293 A-to-I Human chr14 + 103668871 103668871 103668871 ACGATCTCTGCTCACTGCAAGCTCCACCTCCCAGGTTCACGCCATTCTCCTGCCTCAGCCTCCCG ACGATCTCTGCTCACTGCAAGCTCCACCTCCCGGGTTCACGCCATTCTCCTGCCTCAGCCTCCCG A G AL139300.1,KLC1 Ensembl:ENSG00000256500,Ensembl:ENSG00000126214 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1201043743 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102941,RMVar_hsa_circ_16874,RMVar_hsa_circ_363394,RMVar_hsa_circ_53862,RMVar_hsa_circ_53212,RMVar_hsa_circ_112770,RMVar_hsa_circ_370173,RMVar_hsa_circ_169566,RMVar_hsa_circ_373540,RMVar_hsa_circ_299927,RMVar_hsa_circ_345738,RMVar_hsa_circ_108065,RMVar_hsa_circ_109160,RMVar_hsa_circ_103318,RMVar_hsa_circ_169573,RMVar_hsa_circ_90830,RMVar_hsa_circ_99287,RMVar_hsa_circ_90255,RMVar_hsa_circ_169577,RMVar_hsa_circ_81208,RMVar_hsa_circ_84202,RMVar_hsa_circ_169579,RMVar_hsa_circ_169578,RMVar_hsa_circ_169575,RMVar_hsa_circ_169576,RMVar_hsa_circ_169574,RMVar_hsa_circ_169569,RMVar_hsa_circ_169571,RMVar_hsa_circ_169572,RMVar_hsa_circ_169570,RMVar_hsa_circ_169582,RMVar_hsa_circ_169567,RMVar_hsa_circ_169568,RMVar_hsa_circ_97252 7264 RMVar_ID_7264 Human_SNP_ID_568173703 A-to-I Human chr14 + 103681515 103681515 103681515 AGAATCTTGCTCTCTCGCCCAGGCTGGAGTGCAGTCACGCTATCTCGGCTCACTGCAACCTCTGC AGAATCTTGCTCTCTCGCCCAGGCTGGAGTGCGGTCACGCTATCTCGGCTCACTGCAACCTCTGC A G AL139300.1,KLC1 Ensembl:ENSG00000256500,Ensembl:ENSG00000126214 Protein coding,Protein coding intron,intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1418302655 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102941,RMVar_hsa_circ_53862,RMVar_hsa_circ_112770,RMVar_hsa_circ_109160,RMVar_hsa_circ_103318,RMVar_hsa_circ_99287,RMVar_hsa_circ_84202,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_45105,RMVar_hsa_circ_366606,RMVar_hsa_circ_116514,RMVar_hsa_circ_169592,RMVar_hsa_circ_63011,RMVar_hsa_circ_169593,RMVar_hsa_circ_43006,RMVar_hsa_circ_92719,RMVar_hsa_circ_8553 7265 RMVar_ID_7265 Human_SNP_ID_568173706 A-to-I Human chr14 + 103681524 103681524 103681524 CTCTCTCGCCCAGGCTGGAGTGCAGTCACGCTATCTCGGCTCACTGCAACCTCTGCCTCCTGGTT CTCTCTCGCCCAGGCTGGAGTGCAGTCACGCTGTCTCGGCTCACTGCAACCTCTGCCTCCTGGTT A G AL139300.1,KLC1 Ensembl:ENSG00000256500,Ensembl:ENSG00000126214 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs551468115 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102941,RMVar_hsa_circ_53862,RMVar_hsa_circ_112770,RMVar_hsa_circ_109160,RMVar_hsa_circ_103318,RMVar_hsa_circ_99287,RMVar_hsa_circ_84202,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_45105,RMVar_hsa_circ_366606,RMVar_hsa_circ_116514,RMVar_hsa_circ_169592,RMVar_hsa_circ_63011,RMVar_hsa_circ_169593,RMVar_hsa_circ_43006,RMVar_hsa_circ_92719,RMVar_hsa_circ_8553 7266 RMVar_ID_7266 Human_SNP_ID_568173990 A-to-I Human chr14 + 103682514 103682512 103682514 TGAGACCAGCTTGGCCAACATGGGGAAACTCTATCTCTACTAAAAATGCAAAAATTAGCTGGGCA TGAGACCAGCTTGGCCAACATGGGGAAACTC__TCTCTACTAAAAATGCAAAAATTAGCTGGGCA CTA C AL139300.1,KLC1 Ensembl:ENSG00000256500,Ensembl:ENSG00000126214 Protein coding,Protein coding intron,intron GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs1462863487 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_102941,RMVar_hsa_circ_53862,RMVar_hsa_circ_112770,RMVar_hsa_circ_109160,RMVar_hsa_circ_103318,RMVar_hsa_circ_99287,RMVar_hsa_circ_84202,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_45105,RMVar_hsa_circ_366606,RMVar_hsa_circ_116514,RMVar_hsa_circ_169592,RMVar_hsa_circ_63011,RMVar_hsa_circ_169593,RMVar_hsa_circ_43006,RMVar_hsa_circ_92719,RMVar_hsa_circ_8553 7267 RMVar_ID_7267 Human_SNP_ID_568173991 A-to-I Human chr14 + 103682514 103682514 103682514 TGAGACCAGCTTGGCCAACATGGGGAAACTCTATCTCTACTAAAAATGCAAAAATTAGCTGGGCA TGAGACCAGCTTGGCCAACATGGGGAAACTCTCTCTCTACTAAAAATGCAAAAATTAGCTGGGCA A C AL139300.1,KLC1 Ensembl:ENSG00000256500,Ensembl:ENSG00000126214 Protein coding,Protein coding intron,intron GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs554930763 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102941,RMVar_hsa_circ_53862,RMVar_hsa_circ_112770,RMVar_hsa_circ_109160,RMVar_hsa_circ_103318,RMVar_hsa_circ_99287,RMVar_hsa_circ_84202,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_45105,RMVar_hsa_circ_366606,RMVar_hsa_circ_116514,RMVar_hsa_circ_169592,RMVar_hsa_circ_63011,RMVar_hsa_circ_169593,RMVar_hsa_circ_43006,RMVar_hsa_circ_92719,RMVar_hsa_circ_8553 7268 RMVar_ID_7268 Human_SNP_ID_568173992 A-to-I Human chr14 + 103682514 103682514 103682514 TGAGACCAGCTTGGCCAACATGGGGAAACTCTATCTCTACTAAAAATGCAAAAATTAGCTGGGCA TGAGACCAGCTTGGCCAACATGGGGAAACTCTGTCTCTACTAAAAATGCAAAAATTAGCTGGGCA A G AL139300.1,KLC1 Ensembl:ENSG00000256500,Ensembl:ENSG00000126214 Protein coding,Protein coding intron,intron GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs554930763 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102941,RMVar_hsa_circ_53862,RMVar_hsa_circ_112770,RMVar_hsa_circ_109160,RMVar_hsa_circ_103318,RMVar_hsa_circ_99287,RMVar_hsa_circ_84202,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_45105,RMVar_hsa_circ_366606,RMVar_hsa_circ_116514,RMVar_hsa_circ_169592,RMVar_hsa_circ_63011,RMVar_hsa_circ_169593,RMVar_hsa_circ_43006,RMVar_hsa_circ_92719,RMVar_hsa_circ_8553 7269 RMVar_ID_7269 Human_SNP_ID_568174419 A-to-I Human chr14 + 103684039 103684039 103684039 GTCTGTGCGAAAAAAACAAAAATCAGCCAGGCATGGTCGTGCGCGCCTGTAATCCCAGTTACTCA GTCTGTGCGAAAAAAACAAAAATCAGCCAGGCCTGGTCGTGCGCGCCTGTAATCCCAGTTACTCA A C AL139300.1,KLC1 Ensembl:ENSG00000256500,Ensembl:ENSG00000126214 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1319001388 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12283896 RMVar_hsa_circ_102941,RMVar_hsa_circ_53862,RMVar_hsa_circ_112770,RMVar_hsa_circ_109160,RMVar_hsa_circ_103318,RMVar_hsa_circ_99287,RMVar_hsa_circ_84202,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_45105,RMVar_hsa_circ_366606,RMVar_hsa_circ_116514,RMVar_hsa_circ_169592,RMVar_hsa_circ_63011,RMVar_hsa_circ_169593,RMVar_hsa_circ_43006,RMVar_hsa_circ_92719,RMVar_hsa_circ_8553 7270 RMVar_ID_7270 Human_SNP_ID_568175925 A-to-I Human chr14 + 103690069 103690069 103690069 GGGCCAGGTGGTGCATGCCTGTGGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTGGAA GGGCCAGGTGGTGCATGCCTGTGGTCCCAGCTTCTCAGGAGGCTGAGGCAGGAGAATCACTGGAA A T KLC1 Ensembl:ENSG00000126214 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs555964943 Functional Loss SNV dbSNP153 33..33 33 - - - 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_63011,RMVar_hsa_circ_169593,RMVar_hsa_circ_43006,RMVar_hsa_circ_92719 7271 RMVar_ID_7271 Human_SNP_ID_568175926 A-to-I Human chr14 + 103690076 103690076 103690076 GTGGTGCATGCCTGTGGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTGGAACCCAGTA GTGGTGCATGCCTGTGGTCCCAGCTACTCAGGGGGCTGAGGCAGGAGAATCACTGGAACCCAGTA A G KLC1 Ensembl:ENSG00000126214 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs941108825 Functional Loss SNV dbSNP153 33..33 33 - - - 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_63011,RMVar_hsa_circ_169593,RMVar_hsa_circ_43006,RMVar_hsa_circ_92719 7272 RMVar_ID_7272 Human_SNP_ID_568175939 A-to-I Human chr14 + 103690130 103690130 103690130 GGAACCCAGTAGGGCAGAGGTTGCAGTGAGCCAAGATCACACCACTGCACTCCAGCCTGGGCGAT GGAACCCAGTAGGGCAGAGGTTGCAGTGAGCCGAGATCACACCACTGCACTCCAGCCTGGGCGAT A G KLC1 Ensembl:ENSG00000126214 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs893509473 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9783185,Human_RBP_ID_22921553,Human_RBP_ID_25085665 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_63011,RMVar_hsa_circ_169593,RMVar_hsa_circ_43006,RMVar_hsa_circ_92719 7273 RMVar_ID_7273 Human_SNP_ID_568177677 A-to-I Human chr14 + 103696040 103696039 103696040 CTGTGTGTGGTCGTTCTGGTGAGAGGAACCCCACGCGAGAGTCAGCACCTGTTTCTTCAGAGTTG CTGTGTGTGGTCGTTCTGGTGAGAGGAACCCTGCGCGAGAGTCAGCACCTGTTTCTTCAGAGTTG CA TG KLC1 Ensembl:ENSG00000126214 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs386780975 Functional Loss MNV dbSNP153 32..33 33 - - - Human_RBP_ID_5315920,Human_RBP_ID_25085699 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 7274 RMVar_ID_7274 Human_SNP_ID_568177678 A-to-I Human chr14 + 103696040 103696039 103696040 CTGTGTGTGGTCGTTCTGGTGAGAGGAACCCCACGCGAGAGTCAGCACCTGTTTCTTCAGAGTTG CTGTGTGTGGTCGTTCTGGTGAGAGGAACCCC_CGCGAGAGTCAGCACCTGTTTCTTCAGAGTTG CA C KLC1 Ensembl:ENSG00000126214 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1555426075 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5315920,Human_RBP_ID_25085699 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 7275 RMVar_ID_7275 Human_SNP_ID_568177680 A-to-I Human chr14 + 103696040 103696040 103696040 CTGTGTGTGGTCGTTCTGGTGAGAGGAACCCCACGCGAGAGTCAGCACCTGTTTCTTCAGAGTTG CTGTGTGTGGTCGTTCTGGTGAGAGGAACCCCCCGCGAGAGTCAGCACCTGTTTCTTCAGAGTTG A C KLC1 Ensembl:ENSG00000126214 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs861543 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5315920,Human_RBP_ID_25085699 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 7276 RMVar_ID_7276 Human_SNP_ID_568177681 A-to-I Human chr14 + 103696040 103696040 103696040 CTGTGTGTGGTCGTTCTGGTGAGAGGAACCCCACGCGAGAGTCAGCACCTGTTTCTTCAGAGTTG CTGTGTGTGGTCGTTCTGGTGAGAGGAACCCCGCGCGAGAGTCAGCACCTGTTTCTTCAGAGTTG A G KLC1 Ensembl:ENSG00000126214 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs861543 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5315920,Human_RBP_ID_25085699 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 7277 RMVar_ID_7277 Human_SNP_ID_568177682 A-to-I Human chr14 + 103696040 103696040 103696040 CTGTGTGTGGTCGTTCTGGTGAGAGGAACCCCACGCGAGAGTCAGCACCTGTTTCTTCAGAGTTG CTGTGTGTGGTCGTTCTGGTGAGAGGAACCCCTCGCGAGAGTCAGCACCTGTTTCTTCAGAGTTG A T KLC1 Ensembl:ENSG00000126214 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs861543 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5315920,Human_RBP_ID_25085699 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 7278 RMVar_ID_7278 Human_SNP_ID_568183686 A-to-I Human chr14 - 103714682 103714682 103714682 GAAAAAGACTCCATCTCAGAAAGCACACAAAAAAAAGAAGAAAATGTTTGTTCATCCTGCCTTTA GAAAAAGACTCCATCTCAGAAAGCACACAAAATAAAGAAGAAAATGTTTGTTCATCCTGCCTTTA T A XRCC3 Ensembl:ENSG00000126215 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1346515174 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1815579,Human_RBP_ID_18646315,Human_RBP_ID_22921585 7279 RMVar_ID_7279 Human_SNP_ID_568183687 A-to-I Human chr14 - 103714685 103714685 103714685 ACAGAAAAAGACTCCATCTCAGAAAGCACACAAAAAAAAGAAGAAAATGTTTGTTCATCCTGCCT ACAGAAAAAGACTCCATCTCAGAAAGCACACAGAAAAAAGAAGAAAATGTTTGTTCATCCTGCCT T C XRCC3 Ensembl:ENSG00000126215 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs148235356 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1273988,Human_RBP_ID_9758486,Human_RBP_ID_22921586,Human_RBP_ID_23160463,Human_RBP_ID_25124882 7280 RMVar_ID_7280 Human_SNP_ID_568183688 A-to-I Human chr14 - 103714685 103714685 103714685 ACAGAAAAAGACTCCATCTCAGAAAGCACACAAAAAAAAGAAGAAAATGTTTGTTCATCCTGCCT ACAGAAAAAGACTCCATCTCAGAAAGCACACACAAAAAAGAAGAAAATGTTTGTTCATCCTGCCT T G XRCC3 Ensembl:ENSG00000126215 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs148235356 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1273988,Human_RBP_ID_9758486,Human_RBP_ID_22921586,Human_RBP_ID_23160463,Human_RBP_ID_25124882 7281 RMVar_ID_7281 Human_SNP_ID_568238082 A-to-I Human chr14 - 103914580 103914580 103914580 CCCAGGCTGGTCTTGAACTCCTGGGCTCAAGCAGTCCTCCAATCTTGGCTTCCCAAAGTGCTGGA CCCAGGCTGGTCTTGAACTCCTGGGCTCAAGCGGTCCTCCAATCTTGGCTTCCCAAAGTGCTGGA T C ATP5MPL Ensembl:ENSG00000156411 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs747749027 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1559810,Human_Splice_Rec_1559848,Human_Splice_Rec_1559854 RMVar_hsa_circ_112952,RMVar_hsa_circ_81085,RMVar_hsa_circ_92576,RMVar_hsa_circ_169619,RMVar_hsa_circ_169620,RMVar_hsa_circ_356888,RMVar_hsa_circ_169621 7282 RMVar_ID_7282 Human_SNP_ID_568238425 A-to-I Human chr14 - 103915529 103915529 103915529 CAGCCTGGCCAACATGGCAAAACCCTCTCTCTACTAAAAATACAAAAATTAGCCAGGCGTGGTGG CAGCCTGGCCAACATGGCAAAACCCTCTCTCTCCTAAAAATACAAAAATTAGCCAGGCGTGGTGG T G ATP5MPL Ensembl:ENSG00000156411 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs559774346 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81085,RMVar_hsa_circ_169620 7283 RMVar_ID_7283 Human_SNP_ID_568238669 A-to-I Human chr14 - 103916515 103916515 103916515 TTACCCAAATTAGTCTCGAGCTCCTGGACTCAAGTGACCCTCCCACATCAGCCTCCCAAAGCGCT TTACCCAAATTAGTCTCGAGCTCCTGGACTCATGTGACCCTCCCACATCAGCCTCCCAAAGCGCT T A ATP5MPL Ensembl:ENSG00000156411 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1452607884 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12285964 RMVar_hsa_circ_81085,RMVar_hsa_circ_169620 7284 RMVar_ID_7284 Human_SNP_ID_568469910 A-to-I Human chr14 + 104746306 104746306 104746306 GAAACGCTGCCTGGGTGGAAAGCAGACACCACAGGCGCCAGGAGGTGGGAGGACCTGCCCCCACA GAAACGCTGCCTGGGTGGAAAGCAGACACCACGGGCGCCAGGAGGTGGGAGGACCTGCCCCCACA A G ADSS1 Ensembl:ENSG00000185100 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs532710620 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1560500,Human_Splice_Rec_1560501,Human_Splice_Rec_1560540,Human_Splice_Rec_1560541,Human_Splice_Rec_1560564,Human_Splice_Rec_1560565,Human_Splice_Rec_1560584,Human_Splice_Rec_1560585,Human_Splice_Rec_1560594,Human_Splice_Rec_1560595,Human_Splice_Rec_1560597,Human_Splice_Rec_1560600,Human_Splice_Rec_1560601,Human_Splice_Rec_1560603,Human_Splice_Rec_1560605 RMVar_hsa_circ_28385 7285 RMVar_ID_7285 Human_SNP_ID_568495495 A-to-I Human chr14 + 104833235 104833235 104833235 AGACAGGTGCCACCAAGCCTGGCTAATTTTTTATATTTTTAGTAGAGACCGGGTTTCACTGTGTT AGACAGGTGCCACCAAGCCTGGCTAATTTTTTGTATTTTTAGTAGAGACCGGGTTTCACTGTGTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917033176 Functional Loss SNV dbSNP153 33..33 33 - - - 7286 RMVar_ID_7286 Human_SNP_ID_568526134 A-to-I Human chr14 - 104937521 104937521 104937521 TTTGTTGAATGCCTCACTAATGGCAAGTTTCAAGATGTTTTGGGTGACAATGCACACATGCTGGG TTTGTTGAATGCCTCACTAATGGCAAGTTTCAGGATGTTTTGGGTGACAATGCACACATGCTGGG T C AHNAK2 Ensembl:ENSG00000185567 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1301630348 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_442218,Human_RBP_ID_23614218 Human_miRNA_ID_1689123 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 7287 RMVar_ID_7287 Human_SNP_ID_568531216 A-to-I Human chr14 - 104946577 104946577 104946577 GTCGAGGCCCCGAGAGCAAAGCTGGATGGTGCACGGCTGGAGGGTGACCTGTCCCTGGCCGACAA GTCGAGGCCCCGAGAGCAAAGCTGGATGGTGCGCGGCTGGAGGGTGACCTGTCCCTGGCCGACAA T C AHNAK2 Ensembl:ENSG00000185567 Protein coding exon GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs781664318 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2514973,Human_miRNA_ID_2974308,Human_miRNA_ID_3007497 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 7288 RMVar_ID_7288 Human_SNP_ID_568531217 A-to-I Human chr14 - 104946577 104946577 104946577 GTCGAGGCCCCGAGAGCAAAGCTGGATGGTGCACGGCTGGAGGGTGACCTGTCCCTGGCCGACAA GTCGAGGCCCCGAGAGCAAAGCTGGATGGTGCCCGGCTGGAGGGTGACCTGTCCCTGGCCGACAA T G AHNAK2 Ensembl:ENSG00000185567 Protein coding exon GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs781664318 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2514973,Human_miRNA_ID_2974308,Human_miRNA_ID_3007497 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 7289 RMVar_ID_7289 Human_SNP_ID_568531236 A-to-I Human chr14 - 104946597 104946597 104946597 TGCCCAGCGTGGAGGTGGACGTCGAGGCCCCGAGAGCAAAGCTGGATGGTGCACGGCTGGAGGGT TGCCCAGCGTGGAGGTGGACGTCGAGGCCCCGGGAGCAAAGCTGGATGGTGCACGGCTGGAGGGT T C AHNAK2 Ensembl:ENSG00000185567 Protein coding exon GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1297173134 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2898927 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 7290 RMVar_ID_7290 Human_SNP_ID_568550155 A-to-I Human chr14 - 104998552 104998552 104998552 GAAAAACAAAAAACAAAAAGAGAGGCCAAGGCAGGAAGACTGCTTGAGCTCAGGAGTTCAAAACC GAAAAACAAAAAACAAAAAGAGAGGCCAAGGCCGGAAGACTGCTTGAGCTCAGGAGTTCAAAACC T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1484323801 Functional Loss SNV dbSNP153 33..33 33 - - - 7291 RMVar_ID_7291 Human_SNP_ID_97026182 A-to-I Human chr2 - 151250487 151250487 151250487 TCACACCATTCTCCTGCCTCAACCTCTGGAGTAGCTGGGACTACAGGTGCCCACCACCACGCCCG TCACACCATTCTCCTGCCTCAACCTCTGGAGTGGCTGGGACTACAGGTGCCCACCACCACGCCCG T C RBM43 Ensembl:ENSG00000184898 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1383926193 Functional Loss SNV dbSNP153 33..33 33 - - - 7292 RMVar_ID_7292 Human_SNP_ID_97033341 A-to-I Human chr2 - 151280079 151280079 151280079 GCGATTCTCCTGCCTCAGCCTCCTGAATAGCCAGGATTACAGGCGTTTGCCACCACGCCCAGCTA GCGATTCTCCTGCCTCAGCCTCCTGAATAGCCGGGATTACAGGCGTTTGCCACCACGCCCAGCTA T C NMI Ensembl:ENSG00000123609 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1475279403 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_52362,RMVar_hsa_circ_355000,RMVar_hsa_circ_203795,RMVar_hsa_circ_101799,RMVar_hsa_circ_118116,RMVar_hsa_circ_203797 7293 RMVar_ID_7293 Human_SNP_ID_97068293 A-to-I Human chr2 + 151418388 151418388 151418388 CACCACACCTGGCAAATTTTTGTATTTTTAGCAGAGACAGGGTTTTGCCACGTTGGCCAGTCTGG CACCACACCTGGCAAATTTTTGTATTTTTAGCGGAGACAGGGTTTTGCCACGTTGGCCAGTCTGG A G RIF1 Ensembl:ENSG00000080345 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs770708104 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3030,RMVar_hsa_circ_12233,RMVar_hsa_circ_26364,RMVar_hsa_circ_62785,RMVar_hsa_circ_359352,RMVar_hsa_circ_371158,RMVar_hsa_circ_51202,RMVar_hsa_circ_4299,RMVar_hsa_circ_9290,RMVar_hsa_circ_203800,RMVar_hsa_circ_275934,RMVar_hsa_circ_309258,RMVar_hsa_circ_318295,RMVar_hsa_circ_313333,RMVar_hsa_circ_303696,RMVar_hsa_circ_7498,RMVar_hsa_circ_7957,RMVar_hsa_circ_203801,RMVar_hsa_circ_203803,RMVar_hsa_circ_203802,RMVar_hsa_circ_82174,RMVar_hsa_circ_203805 7294 RMVar_ID_7294 Human_SNP_ID_97068400 A-to-I Human chr2 + 151418807 151418807 151418807 GAGGCATTGAGAATCACTTGCACCCGGGAGGCAGAGGTTGCAGTGAGCTGAGATTGCACCACTGC GAGGCATTGAGAATCACTTGCACCCGGGAGGCGGAGGTTGCAGTGAGCTGAGATTGCACCACTGC A G RIF1 Ensembl:ENSG00000080345 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1263810588 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3030,RMVar_hsa_circ_12233,RMVar_hsa_circ_26364,RMVar_hsa_circ_62785,RMVar_hsa_circ_359352,RMVar_hsa_circ_371158,RMVar_hsa_circ_51202,RMVar_hsa_circ_4299,RMVar_hsa_circ_9290,RMVar_hsa_circ_203800,RMVar_hsa_circ_275934,RMVar_hsa_circ_309258,RMVar_hsa_circ_318295,RMVar_hsa_circ_313333,RMVar_hsa_circ_303696,RMVar_hsa_circ_7498,RMVar_hsa_circ_7957,RMVar_hsa_circ_203801,RMVar_hsa_circ_203803,RMVar_hsa_circ_203802,RMVar_hsa_circ_82174,RMVar_hsa_circ_203805 7295 RMVar_ID_7295 Human_SNP_ID_97068980 A-to-I Human chr2 + 151420635 151420635 151420635 GGCATGCGCCTGTAGTCTCAGATGCTTGGGAGACTAAGGCGGGAGGGTTGCTTGACCAGAAATTT GGCATGCGCCTGTAGTCTCAGATGCTTGGGAGCCTAAGGCGGGAGGGTTGCTTGACCAGAAATTT A C RIF1 Ensembl:ENSG00000080345 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs12693029 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3030,RMVar_hsa_circ_12233,RMVar_hsa_circ_26364,RMVar_hsa_circ_62785,RMVar_hsa_circ_371158,RMVar_hsa_circ_51202,RMVar_hsa_circ_4299,RMVar_hsa_circ_9290,RMVar_hsa_circ_203800,RMVar_hsa_circ_309258,RMVar_hsa_circ_318295,RMVar_hsa_circ_313333,RMVar_hsa_circ_303696,RMVar_hsa_circ_7498,RMVar_hsa_circ_35615,RMVar_hsa_circ_7957,RMVar_hsa_circ_203801,RMVar_hsa_circ_203802,RMVar_hsa_circ_82174,RMVar_hsa_circ_88261,RMVar_hsa_circ_296246,RMVar_hsa_circ_335371,RMVar_hsa_circ_203805,RMVar_hsa_circ_308025,RMVar_hsa_circ_290258,RMVar_hsa_circ_46562,RMVar_hsa_circ_203807,RMVar_hsa_circ_203809,RMVar_hsa_circ_203810,RMVar_hsa_circ_203811,RMVar_hsa_circ_203808,RMVar_hsa_circ_203806 7296 RMVar_ID_7296 Human_SNP_ID_97068981 A-to-I Human chr2 + 151420635 151420635 151420635 GGCATGCGCCTGTAGTCTCAGATGCTTGGGAGACTAAGGCGGGAGGGTTGCTTGACCAGAAATTT GGCATGCGCCTGTAGTCTCAGATGCTTGGGAGGCTAAGGCGGGAGGGTTGCTTGACCAGAAATTT A G RIF1 Ensembl:ENSG00000080345 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs12693029 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3030,RMVar_hsa_circ_12233,RMVar_hsa_circ_26364,RMVar_hsa_circ_62785,RMVar_hsa_circ_371158,RMVar_hsa_circ_51202,RMVar_hsa_circ_4299,RMVar_hsa_circ_9290,RMVar_hsa_circ_203800,RMVar_hsa_circ_309258,RMVar_hsa_circ_318295,RMVar_hsa_circ_313333,RMVar_hsa_circ_303696,RMVar_hsa_circ_7498,RMVar_hsa_circ_35615,RMVar_hsa_circ_7957,RMVar_hsa_circ_203801,RMVar_hsa_circ_203802,RMVar_hsa_circ_82174,RMVar_hsa_circ_88261,RMVar_hsa_circ_296246,RMVar_hsa_circ_335371,RMVar_hsa_circ_203805,RMVar_hsa_circ_308025,RMVar_hsa_circ_290258,RMVar_hsa_circ_46562,RMVar_hsa_circ_203807,RMVar_hsa_circ_203809,RMVar_hsa_circ_203810,RMVar_hsa_circ_203811,RMVar_hsa_circ_203808,RMVar_hsa_circ_203806 7297 RMVar_ID_7297 Human_SNP_ID_97069237 A-to-I Human chr2 + 151421599 151421577 151421599 TTGAAGGTCTTGTTTTGTTTTTTGTTTGAGACAAGGTCTCACTATATTACCCAAGCTGGTCTCGA TTGAAGGTCTT______________________AGGTCTCACTATATTACCCAAGCTGGTCTCGA TGTTTTGTTTTTTGTTTGAGACA T RIF1 Ensembl:ENSG00000080345 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1014642120 Functional Loss DEL dbSNP153 12..33 33 - - - Human_RBP_ID_13636657 RMVar_hsa_circ_3030,RMVar_hsa_circ_12233,RMVar_hsa_circ_26364,RMVar_hsa_circ_62785,RMVar_hsa_circ_371158,RMVar_hsa_circ_51202,RMVar_hsa_circ_4299,RMVar_hsa_circ_9290,RMVar_hsa_circ_203800,RMVar_hsa_circ_309258,RMVar_hsa_circ_318295,RMVar_hsa_circ_313333,RMVar_hsa_circ_303696,RMVar_hsa_circ_7498,RMVar_hsa_circ_35615,RMVar_hsa_circ_7957,RMVar_hsa_circ_203801,RMVar_hsa_circ_203802,RMVar_hsa_circ_82174,RMVar_hsa_circ_88261,RMVar_hsa_circ_296246,RMVar_hsa_circ_335371,RMVar_hsa_circ_203805,RMVar_hsa_circ_308025,RMVar_hsa_circ_290258,RMVar_hsa_circ_46562,RMVar_hsa_circ_203807,RMVar_hsa_circ_203809,RMVar_hsa_circ_203810,RMVar_hsa_circ_203811,RMVar_hsa_circ_203808,RMVar_hsa_circ_203806 7298 RMVar_ID_7298 Human_SNP_ID_97071211 A-to-I Human chr2 + 151428095 151428095 151428095 ACAAAACAAAACAAAAATTAGCTGGGCGTGGTAGTATTAGCCAGTAATCCCAGCTACTTGGAAGG ACAAAACAAAACAAAAATTAGCTGGGCGTGGTTGTATTAGCCAGTAATCCCAGCTACTTGGAAGG A T RIF1 Ensembl:ENSG00000080345 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1333502911 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6835464,Human_RBP_ID_25470829 RMVar_hsa_circ_3030,RMVar_hsa_circ_12233,RMVar_hsa_circ_26364,RMVar_hsa_circ_371158,RMVar_hsa_circ_51202,RMVar_hsa_circ_4299,RMVar_hsa_circ_9290,RMVar_hsa_circ_203800,RMVar_hsa_circ_309258,RMVar_hsa_circ_318295,RMVar_hsa_circ_313333,RMVar_hsa_circ_303696,RMVar_hsa_circ_35615,RMVar_hsa_circ_7957,RMVar_hsa_circ_203801,RMVar_hsa_circ_203802,RMVar_hsa_circ_82174,RMVar_hsa_circ_88261,RMVar_hsa_circ_296246,RMVar_hsa_circ_335371,RMVar_hsa_circ_203805,RMVar_hsa_circ_308025,RMVar_hsa_circ_290258,RMVar_hsa_circ_46562,RMVar_hsa_circ_48192,RMVar_hsa_circ_203807,RMVar_hsa_circ_203809,RMVar_hsa_circ_203810,RMVar_hsa_circ_203811,RMVar_hsa_circ_203808,RMVar_hsa_circ_292906,RMVar_hsa_circ_313098,RMVar_hsa_circ_203806,RMVar_hsa_circ_359074,RMVar_hsa_circ_301506,RMVar_hsa_circ_276327,RMVar_hsa_circ_203812,RMVar_hsa_circ_203814,RMVar_hsa_circ_203815,RMVar_hsa_circ_203813 7299 RMVar_ID_7299 Human_SNP_ID_97082906 A-to-I Human chr2 + 151466954 151466954 151466954 ACTTTGAAAGTATTCCTTTGGCCAGGCTCGGTAGCTCACACCTGTAATCCCAGGCATGGGATTTG ACTTTGAAAGTATTCCTTTGGCCAGGCTCGGTGGCTCACACCTGTAATCCCAGGCATGGGATTTG A G RIF1 Ensembl:ENSG00000080345 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs550091499 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4299,RMVar_hsa_circ_82174,RMVar_hsa_circ_88261,RMVar_hsa_circ_203805,RMVar_hsa_circ_203811,RMVar_hsa_circ_47737,RMVar_hsa_circ_99656,RMVar_hsa_circ_36784,RMVar_hsa_circ_203842,RMVar_hsa_circ_30906,RMVar_hsa_circ_45195,RMVar_hsa_circ_83207,RMVar_hsa_circ_203843,RMVar_hsa_circ_311710,RMVar_hsa_circ_203846,RMVar_hsa_circ_203848,RMVar_hsa_circ_203847,RMVar_hsa_circ_203849,RMVar_hsa_circ_62557,RMVar_hsa_circ_203851 7300 RMVar_ID_7300 Human_SNP_ID_97082928 A-to-I Human chr2 + 151467027 151467027 151467027 AGGCAGGTGGATCACCTGAGGGTCGGGAGTTCAAGACCAGCCTGACCAACATGGAGAAACCCCAT AGGCAGGTGGATCACCTGAGGGTCGGGAGTTCGAGACCAGCCTGACCAACATGGAGAAACCCCAT A G RIF1 Ensembl:ENSG00000080345 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs551018041 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4299,RMVar_hsa_circ_82174,RMVar_hsa_circ_88261,RMVar_hsa_circ_203805,RMVar_hsa_circ_203811,RMVar_hsa_circ_47737,RMVar_hsa_circ_99656,RMVar_hsa_circ_36784,RMVar_hsa_circ_203842,RMVar_hsa_circ_30906,RMVar_hsa_circ_45195,RMVar_hsa_circ_83207,RMVar_hsa_circ_203843,RMVar_hsa_circ_311710,RMVar_hsa_circ_203846,RMVar_hsa_circ_203848,RMVar_hsa_circ_203847,RMVar_hsa_circ_203849,RMVar_hsa_circ_62557,RMVar_hsa_circ_203851 7301 RMVar_ID_7301 Human_SNP_ID_97083071 A-to-I Human chr2 + 151467490 151467490 151467490 CCTCAGCCTCTTGAGTAGCTGGCATTACAGGCATGTGCCACTAAGCCCAGCTAATTTTTGTACTT CCTCAGCCTCTTGAGTAGCTGGCATTACAGGCGTGTGCCACTAAGCCCAGCTAATTTTTGTACTT A G RIF1 Ensembl:ENSG00000080345 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1432817555 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4299,RMVar_hsa_circ_82174,RMVar_hsa_circ_88261,RMVar_hsa_circ_203805,RMVar_hsa_circ_203811,RMVar_hsa_circ_47737,RMVar_hsa_circ_99656,RMVar_hsa_circ_36784,RMVar_hsa_circ_203842,RMVar_hsa_circ_30906,RMVar_hsa_circ_45195,RMVar_hsa_circ_83207,RMVar_hsa_circ_203843,RMVar_hsa_circ_311710,RMVar_hsa_circ_203846,RMVar_hsa_circ_203848,RMVar_hsa_circ_203847,RMVar_hsa_circ_203849,RMVar_hsa_circ_62557,RMVar_hsa_circ_203851 7302 RMVar_ID_7302 Human_SNP_ID_97083088 A-to-I Human chr2 + 151467534 151467534 151467534 GCCCAGCTAATTTTTGTACTTTTAGTAGAGATAAGGTTTCACCATGTTGGTCAGGCTGGTCTTGA GCCCAGCTAATTTTTGTACTTTTAGTAGAGATGAGGTTTCACCATGTTGGTCAGGCTGGTCTTGA A G RIF1 Ensembl:ENSG00000080345 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs951282042 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4299,RMVar_hsa_circ_82174,RMVar_hsa_circ_88261,RMVar_hsa_circ_203805,RMVar_hsa_circ_203811,RMVar_hsa_circ_47737,RMVar_hsa_circ_99656,RMVar_hsa_circ_36784,RMVar_hsa_circ_203842,RMVar_hsa_circ_30906,RMVar_hsa_circ_45195,RMVar_hsa_circ_83207,RMVar_hsa_circ_203843,RMVar_hsa_circ_311710,RMVar_hsa_circ_203846,RMVar_hsa_circ_203848,RMVar_hsa_circ_203847,RMVar_hsa_circ_203849,RMVar_hsa_circ_62557,RMVar_hsa_circ_203851 7303 RMVar_ID_7303 Human_SNP_ID_97085861 A-to-I Human chr2 + 151477434 151477434 151477434 GGATTGTCATGTAGTATCTTTTTTTTTTTTTGAGACACAGTCTTGCTCTGTTGCCTATGCTGGAG GGATTGTCATGTAGTATCTTTTTTTTTTTTTGTGACACAGTCTTGCTCTGTTGCCTATGCTGGAG A T RIF1 Ensembl:ENSG00000080345 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1286361227 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2592993,Human_RBP_ID_23181843 RMVar_hsa_circ_203848,RMVar_hsa_circ_360347,RMVar_hsa_circ_348949,RMVar_hsa_circ_203853 7304 RMVar_ID_7304 Human_SNP_ID_97085903 A-to-I Human chr2 + 151477554 151477554 151477554 CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGTGCCCGCCACCATGCCCGGCTAATTTTT CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTGCAGGTGCCCGCCACCATGCCCGGCTAATTTTT A G RIF1 Ensembl:ENSG00000080345 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1308058820 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_203848,RMVar_hsa_circ_360347,RMVar_hsa_circ_348949,RMVar_hsa_circ_203853 7305 RMVar_ID_7305 Human_SNP_ID_97086116 A-to-I Human chr2 + 151478343 151478343 151478343 TCCTGTCTCTACTAAAAATACAAAAACCAGCCAGGCATGTTGGCGCATACTTGTAATCTCAGCTA TCCTGTCTCTACTAAAAATACAAAAACCAGCCCGGCATGTTGGCGCATACTTGTAATCTCAGCTA A C RIF1 Ensembl:ENSG00000080345 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs887644592 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_203848,RMVar_hsa_circ_360347,RMVar_hsa_circ_348949,RMVar_hsa_circ_203853 7306 RMVar_ID_7306 Human_SNP_ID_97086117 A-to-I Human chr2 + 151478343 151478343 151478343 TCCTGTCTCTACTAAAAATACAAAAACCAGCCAGGCATGTTGGCGCATACTTGTAATCTCAGCTA TCCTGTCTCTACTAAAAATACAAAAACCAGCCGGGCATGTTGGCGCATACTTGTAATCTCAGCTA A G RIF1 Ensembl:ENSG00000080345 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs887644592 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_203848,RMVar_hsa_circ_360347,RMVar_hsa_circ_348949,RMVar_hsa_circ_203853 7307 RMVar_ID_7307 Human_SNP_ID_97086134 A-to-I Human chr2 + 151478406 151478406 151478406 TACTCAGGAGGCTGAGACATGAGAATTGCTTGAACCTTTTAGGCGGAGGTTGCAGTGAGCCGAGA TACTCAGGAGGCTGAGACATGAGAATTGCTTGGACCTTTTAGGCGGAGGTTGCAGTGAGCCGAGA A G RIF1 Ensembl:ENSG00000080345 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs772314308 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13638245 RMVar_hsa_circ_203848,RMVar_hsa_circ_360347,RMVar_hsa_circ_348949,RMVar_hsa_circ_203853 7308 RMVar_ID_7308 Human_SNP_ID_97086142 A-to-I Human chr2 + 151478441 151478441 151478441 CTTTTAGGCGGAGGTTGCAGTGAGCCGAGATCATGCCATTGCGCGACAGAGCAAGTCTCTGTCTC CTTTTAGGCGGAGGTTGCAGTGAGCCGAGATCGTGCCATTGCGCGACAGAGCAAGTCTCTGTCTC A G RIF1 Ensembl:ENSG00000080345 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1012276604 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569953,Human_RBP_ID_25471393 RMVar_hsa_circ_203848,RMVar_hsa_circ_360347,RMVar_hsa_circ_348949,RMVar_hsa_circ_203853 7309 RMVar_ID_7309 Human_SNP_ID_97152005 A-to-I Human chr2 - 151756360 151756360 151756360 GGTCTCTGTTAGGGCTCCTGGTCTGAACCTTTAAGTGGCTATGGCAAAGCAACAATGGGCCTTGT GGTCTCTGTTAGGGCTCCTGGTCTGAACCTTTGAGTGGCTATGGCAAAGCAACAATGGGCCTTGT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs975178454 Functional Loss SNV dbSNP153 33..33 33 - - - 7310 RMVar_ID_7310 Human_SNP_ID_97160274 A-to-I Human chr2 - 151790976 151790976 151790976 AACACCCAAAGGGGCTGGGTGTGGTGGCTCACACCTGTAATGTCAGCACTTTGGGAGGCCCAGGC AACACCCAAAGGGGCTGGGTGTGGTGGCTCACGCCTGTAATGTCAGCACTTTGGGAGGCCCAGGC T C ARL5A Ensembl:ENSG00000162980 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924276371 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_52869,RMVar_hsa_circ_372353,RMVar_hsa_circ_336360,RMVar_hsa_circ_203859 7311 RMVar_ID_7311 Human_SNP_ID_97190346 A-to-I Human chr2 - 151919300 151919300 151919300 TTGAGCCCAGGAGTGTGAGGCTGCAGTGAGCTATGACTGTGCCACAGTACTCCAGCCTGGATGAA TTGAGCCCAGGAGTGTGAGGCTGCAGTGAGCTGTGACTGTGCCACAGTACTCCAGCCTGGATGAA T C AC068547.1,CACNB4 Ensembl:ENSG00000283228,Ensembl:ENSG00000182389 Protein coding,Protein coding intron,intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1035372623 Functional Loss SNV dbSNP153 33..33 33 - - - 7312 RMVar_ID_7312 Human_SNP_ID_97190776 A-to-I Human chr2 - 151920882 151920882 151920882 CGTCCGCCTTGGCCTCCCAAAGTGCTAGGATTACAGGCGTGAGTCACCGTGCCTGGCCTCAAGTA CGTCCGCCTTGGCCTCCCAAAGTGCTAGGATTGCAGGCGTGAGTCACCGTGCCTGGCCTCAAGTA T C AC068547.1,CACNB4 Ensembl:ENSG00000283228,Ensembl:ENSG00000182389 Protein coding,Protein coding intron,intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs557581245 Functional Loss SNV dbSNP153 33..33 33 - - - 7313 RMVar_ID_7313 Human_SNP_ID_97218989 A-to-I Human chr2 - 152043958 152043958 152043958 CAAGTGATCCTCTCACCTTAGTCTCCTGAGTAACTGGGACTATAGGAATGTGCCATCAAGCCCGG CAAGTGATCCTCTCACCTTAGTCTCCTGAGTAGCTGGGACTATAGGAATGTGCCATCAAGCCCGG T C CACNB4 Ensembl:ENSG00000182389 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1207246211 Functional Loss SNV dbSNP153 33..33 33 - - - 7314 RMVar_ID_7314 Human_SNP_ID_97235835 A-to-I Human chr2 - 152115569 152115569 152115569 TATCCTAATAAAGGCTTTCCGGTTGGCTGGGCATGGTGGCTCACACTTCTAATCCCAGCACTTTG TATCCTAATAAAGGCTTTCCGGTTGGCTGGGCGTGGTGGCTCACACTTCTAATCCCAGCACTTTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1052562859 Functional Loss SNV dbSNP153 33..33 33 - - - 7315 RMVar_ID_7315 Human_SNP_ID_97237950 A-to-I Human chr2 - 152123940 152123940 152123940 GAGATGAGTGAATCAACTTTTTCTTTCTGATTAATAGACATATCCAGTTCAATCACATGGTGGAA GAGATGAGTGAATCAACTTTTTCTTTCTGATTTATAGACATATCCAGTTCAATCACATGGTGGAA T A STAM2 Ensembl:ENSG00000115145 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348995835 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_203871,RMVar_hsa_circ_89636,RMVar_hsa_circ_203875,RMVar_hsa_circ_292682,RMVar_hsa_circ_306270,RMVar_hsa_circ_308169,RMVar_hsa_circ_310042,RMVar_hsa_circ_297840,RMVar_hsa_circ_281494,RMVar_hsa_circ_203873,RMVar_hsa_circ_203874,RMVar_hsa_circ_203872 7316 RMVar_ID_7316 Human_SNP_ID_97239183 A-to-I Human chr2 - 152129285 152129285 152129285 ATGATTAGCTGGGCTTGGTGGTGTGCGCCTGTAGTCCCAGCTCCTCAAGAAGCTGAGGTGGGAAG ATGATTAGCTGGGCTTGGTGGTGTGCGCCTGTCGTCCCAGCTCCTCAAGAAGCTGAGGTGGGAAG T G STAM2 Ensembl:ENSG00000115145 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1391358982 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_137,RMVar_hsa_circ_203871,RMVar_hsa_circ_89636,RMVar_hsa_circ_203875,RMVar_hsa_circ_292682,RMVar_hsa_circ_308169,RMVar_hsa_circ_310042,RMVar_hsa_circ_297840,RMVar_hsa_circ_281494,RMVar_hsa_circ_203873,RMVar_hsa_circ_203874,RMVar_hsa_circ_331911,RMVar_hsa_circ_203872,RMVar_hsa_circ_269081,RMVar_hsa_circ_203876 7317 RMVar_ID_7317 Human_SNP_ID_97244829 A-to-I Human chr2 - 152152061 152152061 152152061 TGGTGCACACCTGTAGTCCTAGCTACTCGGGAAGCTGAGGTGGGAGGATCACGTGAGCCCCGGGA TGGTGCACACCTGTAGTCCTAGCTACTCGGGAGGCTGAGGTGGGAGGATCACGTGAGCCCCGGGA T C STAM2 Ensembl:ENSG00000115145 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968105365 Functional Loss SNV dbSNP153 33..33 33 - - - 7318 RMVar_ID_7318 Human_SNP_ID_97244847 A-to-I Human chr2 - 152152123 152152123 152152123 GAACCTGGGCAACATGGCAAAACCCCGTCTCCACAAAAAATACGAAACTTAGTTGGGCGTGATGG GAACCTGGGCAACATGGCAAAACCCCGTCTCCGCAAAAAATACGAAACTTAGTTGGGCGTGATGG T C STAM2 Ensembl:ENSG00000115145 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs774901419 Functional Loss SNV dbSNP153 33..33 33 - - - 7319 RMVar_ID_7319 Human_SNP_ID_97244866 A-to-I Human chr2 - 152152205 152152205 152152205 TGGGCATGATGGCTCAAACTAGTAATCTCAGCACTTTGGGAGGCCGAGGTGGGCAGATCATTTGA TGGGCATGATGGCTCAAACTAGTAATCTCAGCTCTTTGGGAGGCCGAGGTGGGCAGATCATTTGA T A STAM2 Ensembl:ENSG00000115145 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs949185314 Functional Loss SNV dbSNP153 33..33 33 - - - 7320 RMVar_ID_7320 Human_SNP_ID_97248731 A-to-I Human chr2 - 152166081 152166081 152166081 CACCCTCCACCTCCCAGGTTCAATCTGGGACTACAGATGTGCACCACCATGCCTGGCTAGTTTTT CACCCTCCACCTCCCAGGTTCAATCTGGGACTGCAGATGTGCACCACCATGCCTGGCTAGTTTTT T C STAM2 Ensembl:ENSG00000115145 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs980404389 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13642002 7321 RMVar_ID_7321 Human_SNP_ID_97290893 A-to-I Human chr2 + 152346234 152346234 152346234 TGTAGTAGAGACGGGGTTTCATCATGTTGCCCAAGCTGCTCTTGAACTCCCAACCTCAGGTGATC TGTAGTAGAGACGGGGTTTCATCATGTTGCCCGAGCTGCTCTTGAACTCCCAACCTCAGGTGATC A G FMNL2 Ensembl:ENSG00000157827 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs773648958 Functional Loss SNV dbSNP153 33..33 33 - - - 7322 RMVar_ID_7322 Human_SNP_ID_97301532 A-to-I Human chr2 + 152390206 152390206 152390206 TCGGAGCTGGACCTGGTGGTCCCTTTCCGTGTAAACTTCCGGCTGAAAGGGAAGGACATGGTGGT TCGGAGCTGGACCTGGTGGTCCCTTTCCGTGTGAACTTCCGGCTGAAAGGGAAGGACATGGTGGT A G FMNL2,AC012066.1 Ensembl:ENSG00000157827,Ensembl:ENSG00000213197 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1317361953 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5099637,Human_RBP_ID_23119331 7323 RMVar_ID_7323 Human_SNP_ID_97301615 A-to-I Human chr2 - 152390547 152390547 152390547 TCAGAATCTCCTGTTTCTTCTGTTCGTCTGAGATTGGCAGCCCCATGGACTTCTGTCTCTGGTCA TCAGAATCTCCTGTTTCTTCTGTTCGTCTGAGGTTGGCAGCCCCATGGACTTCTGTCTCTGGTCA T C - - Other Unknown GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs893667698 Functional Loss SNV dbSNP153 33..33 33 - - - 7324 RMVar_ID_7324 Human_SNP_ID_97308153 A-to-I Human chr2 + 152419389 152419389 152419389 CATGCTGTGGAATAGCCCTCAAAAAAGGAAGAAATTCTGTCATTTGCGACAACATGAGTGGAATT CATGCTGTGGAATAGCCCTCAAAAAAGGAAGACATTCTGTCATTTGCGACAACATGAGTGGAATT A C FMNL2 Ensembl:ENSG00000157827 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs891038100 Functional Loss SNV dbSNP153 33..33 33 - - - 7325 RMVar_ID_7325 Human_SNP_ID_97355339 A-to-I Human chr2 + 152624257 152624257 152624257 TCGGTGCACTGCAACCTCTGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTTCCGAGTAGC TCGGTGCACTGCAACCTCTGCCTCCCGGGTTCGAGCGATTCTCCTGCCTCAGCCTTCCGAGTAGC A G FMNL2 Ensembl:ENSG00000157827 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1224029013 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23980,RMVar_hsa_circ_124580,RMVar_hsa_circ_203896,RMVar_hsa_circ_104068,RMVar_hsa_circ_203902,RMVar_hsa_circ_67247,RMVar_hsa_circ_203905,RMVar_hsa_circ_37389,RMVar_hsa_circ_47245 7326 RMVar_ID_7326 Human_SNP_ID_97372724 A-to-I Human chr2 - 152689797 152689797 152689797 TTTTTTTTTTTGCTTGTTTGTTTGTTTTTGAGACAGAGTCTCTGTTGCCCAGGCTGGAGTGCAGT TTTTTTTTTTTGCTTGTTTGTTTGTTTTTGAGGCAGAGTCTCTGTTGCCCAGGCTGGAGTGCAGT T C PRPF40A Ensembl:ENSG00000196504 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs971463372 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13644933 RMVar_hsa_circ_42443,RMVar_hsa_circ_79634,RMVar_hsa_circ_203921,RMVar_hsa_circ_203924,RMVar_hsa_circ_113329,RMVar_hsa_circ_63193,RMVar_hsa_circ_90444,RMVar_hsa_circ_347103,RMVar_hsa_circ_203930,RMVar_hsa_circ_339096,RMVar_hsa_circ_203932,RMVar_hsa_circ_15842,RMVar_hsa_circ_24510 7327 RMVar_ID_7327 Human_SNP_ID_97388985 A-to-I Human chr2 + 152747839 152747839 152747839 GTGATCCACCCGCCTTGGCCTCCCAAAGTGCTAGGATTGCAGGCGTGAGCCACCATGCCTGGCCA GTGATCCACCCGCCTTGGCCTCCCAAAGTGCTGGGATTGCAGGCGTGAGCCACCATGCCTGGCCA A G ARL6IP6 Ensembl:ENSG00000177917 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1178704847 Functional Loss SNV dbSNP153 33..33 33 - - - 7328 RMVar_ID_7328 Human_SNP_ID_97894021 A-to-I Human chr2 - 154783466 154783466 154783466 TGAGACAGATCCAGGGTGTTAGTAGTGGCAGGAAAATATAATAAAGAGCCTTTCTCTTGCTGCAT TGAGACAGATCCAGGGTGTTAGTAGTGGCAGGGAAATATAATAAAGAGCCTTTCTCTTGCTGCAT T C lnc-RPRM-10 RNACentral:URS00008BC482 lincRNA intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1015322449 Functional Loss SNV dbSNP153 33..33 33 - - - 7329 RMVar_ID_7329 Human_SNP_ID_97902571 A-to-I Human chr2 + 154821821 154821821 154821821 TGCCACCACACCTGGCTATTTTTTGTATTTTTAGTAGAGACCAGGTTTCACTATGTGGGCCCAGC TGCCACCACACCTGGCTATTTTTTGTATTTTTCGTAGAGACCAGGTTTCACTATGTGGGCCCAGC A C KCNJ3 Ensembl:ENSG00000162989 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1344158362 Functional Loss SNV dbSNP153 33..33 33 - - - 7330 RMVar_ID_7330 Human_SNP_ID_98269900 A-to-I Human chr2 + 156361256 156361256 156361256 GTTGTCCAGGCTGGTCTTGAACTCCTGGCCTCAAGCAGTCCTCCTGCCTTGGACTCCCAAAGTGC GTTGTCCAGGCTGGTCTTGAACTCCTGGCCTCCAGCAGTCCTCCTGCCTTGGACTCCCAAAGTGC A C lnc-GPD2-1,lnc-GPD2-1:2,lnc-GPD2-1:3,lnc-GPD2-1:4,lnc-GPD2-1:5,lnc-GPD2-1:6,lnc-GPD2-1:7,lnc-GPD2-1:8 RNACentral:URS0000D5B7B5,RNACentral:URS0000D5E15D,RNACentral:URS0000D5E179,RNACentral:URS0000D5BA48,RNACentral:URS0000D5C8EA,RNACentral:URS0000D5930A,RNACentral:URS0000D572CA,RNACentral:URS0000D5AD30 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,exon,exon,intron,exon,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs531680138 Functional Loss SNV dbSNP153 33..33 33 - - - 7331 RMVar_ID_7331 Human_SNP_ID_98306085 A-to-I Human chr2 + 156515240 156515240 156515240 AAGACCAACATGGCGAATCCTCATCTCTACTAAAAATACAAGAAATTAGCCAGGTGCGGTGGCAT AAGACCAACATGGCGAATCCTCATCTCTACTACAAATACAAGAAATTAGCCAGGTGCGGTGGCAT A C GPD2 Ensembl:ENSG00000115159 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs773882232 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1642,RMVar_hsa_circ_203948,RMVar_hsa_circ_318252,RMVar_hsa_circ_275700,RMVar_hsa_circ_203946,RMVar_hsa_circ_270059,RMVar_hsa_circ_302205,RMVar_hsa_circ_10400,RMVar_hsa_circ_203950 7332 RMVar_ID_7332 Human_SNP_ID_98306097 A-to-I Human chr2 + 156515281 156515281 156515281 GAAATTAGCCAGGTGCGGTGGCATGCACTTGTAGTCCCAGCTACTTGGGGGGCTGAGGTGGCTGC GAAATTAGCCAGGTGCGGTGGCATGCACTTGTGGTCCCAGCTACTTGGGGGGCTGAGGTGGCTGC A G GPD2 Ensembl:ENSG00000115159 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1371634141 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1642,RMVar_hsa_circ_203948,RMVar_hsa_circ_318252,RMVar_hsa_circ_275700,RMVar_hsa_circ_203946,RMVar_hsa_circ_270059,RMVar_hsa_circ_302205,RMVar_hsa_circ_10400,RMVar_hsa_circ_203950 7333 RMVar_ID_7333 Human_SNP_ID_98617796 A-to-I Human chr2 - 157864493 157864493 157864493 TGTGGTGTCCAAGTGTGATTATAGTGGATCACACCTGTAATCACAGCACTTTGGGAGGCCAAGGC TGTGGTGTCCAAGTGTGATTATAGTGGATCACGCCTGTAATCACAGCACTTTGGGAGGCCAAGGC T C ACVR1 Ensembl:ENSG00000115170 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1434418370 Functional Loss SNV dbSNP153 33..33 33 - - - 7334 RMVar_ID_7334 Human_SNP_ID_98664575 A-to-I Human chr2 + 158065856 158065856 158065856 AAGAACCTCATTGTTGTACTGCTGTTCATTGCATTGCAGGCCTTGGGAGAGCTCCAGTACTTGTT AAGAACCTCATTGTTGTACTGCTGTTCATTGCGTTGCAGGCCTTGGGAGAGCTCCAGTACTTGTT A G UPP2,PTP4A1P1 Ensembl:ENSG00000007001,Ensembl:ENSG00000231158 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1462833003 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_60679,Human_RBP_ID_1900619,Human_RBP_ID_2596571,Human_RBP_ID_4627871,Human_RBP_ID_5099680,Human_RBP_ID_5588694,Human_RBP_ID_6840052,Human_RBP_ID_8258756,Human_RBP_ID_13652002,Human_RBP_ID_17697522,Human_RBP_ID_18534001,Human_RBP_ID_20619398,Human_RBP_ID_22394416,Human_RBP_ID_22813854,Human_RBP_ID_26488022 Human_miRNA_ID_1829758 7335 RMVar_ID_7335 Human_SNP_ID_98768712 A-to-I Human chr2 + 158482349 158482349 158482349 TCCTTCCTTCCTTTCCAAGACATGGTCTTGCTATGTTGCCCAGGCTGGACTCAAACTCCTGGACC TCCTTCCTTCCTTTCCAAGACATGGTCTTGCTCTGTTGCCCAGGCTGGACTCAAACTCCTGGACC A C PKP4 Ensembl:ENSG00000144283 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs547557792 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18948342 RMVar_hsa_circ_203985,RMVar_hsa_circ_76123 7336 RMVar_ID_7336 Human_SNP_ID_98793770 A-to-I Human chr2 - 158584217 158584217 158584217 CAAAGCTGCCATCTGTGGGATTATGACTAAACACCTCTAAGTCAGAATACCGCCCAGGCAGAACC CAAAGCTGCCATCTGTGGGATTATGACTAAACGCCTCTAAGTCAGAATACCGCCCAGGCAGAACC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs78760284 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6840568,Human_RBP_ID_8843153,Human_RBP_ID_26749825,Human_RBP_ID_27158788 7337 RMVar_ID_7337 Human_SNP_ID_98793771 A-to-I Human chr2 - 158584221 158584221 158584221 GGGGCAAAGCTGCCATCTGTGGGATTATGACTAAACACCTCTAAGTCAGAATACCGCCCAGGCAG GGGGCAAAGCTGCCATCTGTGGGATTATGACTGAACACCTCTAAGTCAGAATACCGCCCAGGCAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs79153602 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6840568,Human_RBP_ID_8843153,Human_RBP_ID_26749825,Human_RBP_ID_27158317 7338 RMVar_ID_7338 Human_SNP_ID_98807534 A-to-I Human chr2 + 158643865 158643865 158643865 TGAGCTCACTGCAACCTCTGCCTCCCGGGTTCAAGCGATTCTCTCGCCTCAGCCTCCTGAGTAAC TGAGCTCACTGCAACCTCTGCCTCCCGGGTTCCAGCGATTCTCTCGCCTCAGCCTCCTGAGTAAC A C PKP4 Ensembl:ENSG00000144283 Protein coding intron GSE100210;GSE107867;GSE107867 HepG2 cell line;ASD brains,temporal_cortex;ASD brains,temporal_cortex - 29129909,30559470,30559470 RNA-Seq:(High) rs889163911 Functional Loss SNV dbSNP153 33..33 33 - - - 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 7339 RMVar_ID_7339 Human_SNP_ID_98807535 A-to-I Human chr2 + 158643865 158643865 158643865 TGAGCTCACTGCAACCTCTGCCTCCCGGGTTCAAGCGATTCTCTCGCCTCAGCCTCCTGAGTAAC TGAGCTCACTGCAACCTCTGCCTCCCGGGTTCGAGCGATTCTCTCGCCTCAGCCTCCTGAGTAAC A G PKP4 Ensembl:ENSG00000144283 Protein coding intron GSE100210;GSE107867;GSE107867 HepG2 cell line;ASD brains,temporal_cortex;ASD brains,temporal_cortex - 29129909,30559470,30559470 RNA-Seq:(High) rs889163911 Functional Loss SNV dbSNP153 33..33 33 - - - 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 7340 RMVar_ID_7340 Human_SNP_ID_98807561 A-to-I Human chr2 + 158643946 158643946 158643946 CGCCACCAAACCCAGCTAATTTTTGTATTTTTAGTAGAGATGGAGTCTCACCATGTTGGCCAGAC CGCCACCAAACCCAGCTAATTTTTGTATTTTTGGTAGAGATGGAGTCTCACCATGTTGGCCAGAC A G PKP4 Ensembl:ENSG00000144283 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs906226998 Functional Loss SNV dbSNP153 33..33 33 - - - 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 7341 RMVar_ID_7341 Human_SNP_ID_98807563 A-to-I Human chr2 + 158643966 158643966 158643966 TTTTGTATTTTTAGTAGAGATGGAGTCTCACCATGTTGGCCAGACTGGTCTCCAACTTCTGACCT TTTTGTATTTTTAGTAGAGATGGAGTCTCACCGTGTTGGCCAGACTGGTCTCCAACTTCTGACCT A G PKP4 Ensembl:ENSG00000144283 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251727569 Functional Loss SNV dbSNP153 33..33 33 - - - 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 7342 RMVar_ID_7342 Human_SNP_ID_98892560 A-to-I Human chr2 + 158975670 158975670 158975670 GTTGCCCAGGCTCGTCTCGAACTCCTGGCCTCAAGCAATCCTTCCACCTCAGTTTCCCAAAGTGC GTTGCCCAGGCTCGTCTCGAACTCCTGGCCTCGAGCAATCCTTCCACCTCAGTTTCCCAAAGTGC A G TANC1 Ensembl:ENSG00000115183 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs938775433 Functional Loss SNV dbSNP153 33..33 33 - - - 7343 RMVar_ID_7343 Human_SNP_ID_98899083 A-to-I Human chr2 + 159003900 159003900 159003900 ACTTCAGGCTCAGGTCCAGATAGGGGGCAAGGATACAGCTCGCAGAAAGAAGAAGGTGGTACATA ACTTCAGGCTCAGGTCCAGATAGGGGGCAAGGGTACAGCTCGCAGAAAGAAGAAGGTGGTACATA A G TANC1 Ensembl:ENSG00000115183 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1486900170 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2489628,Human_miRNA_ID_2751706 RMVar_hsa_circ_204014,RMVar_hsa_circ_306123,RMVar_hsa_circ_354222,RMVar_hsa_circ_358287,RMVar_hsa_circ_353754,RMVar_hsa_circ_67915,RMVar_hsa_circ_122905,RMVar_hsa_circ_204016,RMVar_hsa_circ_204015 7344 RMVar_ID_7344 Human_SNP_ID_98899101 A-to-I Human chr2 - 159003972 159003971 159003972 ACCAGCTATATTATTCACAGCCAGTTTTTTTTAGAGAACTCTGAAGCTTTTTGTCATCAGCTGTG ACCAGCTATATTATTCACAGCCAGTTTTTTTT_GAGAACTCTGAAGCTTTTTGTCATCAGCTGTG CT C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs375638271 Functional Loss DEL dbSNP153 33..33 33 - - - 7345 RMVar_ID_7345 Human_SNP_ID_98899949 A-to-I Human chr2 + 159007335 159007335 159007335 CAACCAACTAATTTTGTATCTTTAATAGAGACAGGGTTTTTCCATGTTGGTCAGGCTGGTCTTGA CAACCAACTAATTTTGTATCTTTAATAGAGACGGGGTTTTTCCATGTTGGTCAGGCTGGTCTTGA A G TANC1 Ensembl:ENSG00000115183 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1326921515 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23832403 RMVar_hsa_circ_204014,RMVar_hsa_circ_306123,RMVar_hsa_circ_354222,RMVar_hsa_circ_358287,RMVar_hsa_circ_353754,RMVar_hsa_circ_67915,RMVar_hsa_circ_122905,RMVar_hsa_circ_204016,RMVar_hsa_circ_204015 7346 RMVar_ID_7346 Human_SNP_ID_98917739 A-to-I Human chr2 + 159083128 159083128 159083128 CCATATGTCCAGCTAATTTTTGTATTTTTAGTAGGGATGGGGTTTCACCATGTTGGTTCAAGACC CCATATGTCCAGCTAATTTTTGTATTTTTAGTGGGGATGGGGTTTCACCATGTTGGTTCAAGACC A G TANC1 Ensembl:ENSG00000115183 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909787477 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_204014,RMVar_hsa_circ_306123,RMVar_hsa_circ_358287,RMVar_hsa_circ_67915,RMVar_hsa_circ_204018,RMVar_hsa_circ_296971,RMVar_hsa_circ_324236,RMVar_hsa_circ_270280 7347 RMVar_ID_7347 Human_SNP_ID_98951434 A-to-I Human chr2 + 159220743 159220743 159220743 CCCCTGAGTAGCTGGGAATACAGGCATGCACCACCGTACCTGGCTAATTTTTAGAGACACGGTTT CCCCTGAGTAGCTGGGAATACAGGCATGCACCGCCGTACCTGGCTAATTTTTAGAGACACGGTTT A G TANC1 Ensembl:ENSG00000115183 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1030116249 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97002,RMVar_hsa_circ_204025,RMVar_hsa_circ_76056,RMVar_hsa_circ_204035,RMVar_hsa_circ_110420,RMVar_hsa_circ_204037,RMVar_hsa_circ_7749,RMVar_hsa_circ_117431,RMVar_hsa_circ_76821,RMVar_hsa_circ_204039,RMVar_hsa_circ_204040 7348 RMVar_ID_7348 Human_SNP_ID_98956028 A-to-I Human chr2 - 159236777 159236777 159236777 ACTAAAAATACAAAACATTAGCCAGATGTGGTACCAGGTGCCTGTGATCCCAGCTACTTGGGAGG ACTAAAAATACAAAACATTAGCCAGATGTGGTCCCAGGTGCCTGTGATCCCAGCTACTTGGGAGG T G WDSUB1 Ensembl:ENSG00000196151 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1010664853 Functional Loss SNV dbSNP153 33..33 33 - - - 7349 RMVar_ID_7349 Human_SNP_ID_98956623 A-to-I Human chr2 - 159239173 159239173 159239173 TAATGAGACCCCCTTCTCTACAAAAAATTTTTAAAAATTAGCCAGGTGTTGTGGTGTATGCCTGT TAATGAGACCCCCTTCTCTACAAAAAATTTTTTAAAATTAGCCAGGTGTTGTGGTGTATGCCTGT T A WDSUB1 Ensembl:ENSG00000196151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs574897482 Functional Loss SNV dbSNP153 33..33 33 - - - 7350 RMVar_ID_7350 Human_SNP_ID_98956624 A-to-I Human chr2 - 159239173 159239173 159239173 TAATGAGACCCCCTTCTCTACAAAAAATTTTTAAAAATTAGCCAGGTGTTGTGGTGTATGCCTGT TAATGAGACCCCCTTCTCTACAAAAAATTTTTGAAAATTAGCCAGGTGTTGTGGTGTATGCCTGT T C WDSUB1 Ensembl:ENSG00000196151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs574897482 Functional Loss SNV dbSNP153 33..33 33 - - - 7351 RMVar_ID_7351 Human_SNP_ID_98959345 A-to-I Human chr2 + 159248745 159248744 159248745 CTCCCACCTCAGCCTCCTGAGTAGCTGGGACTACAGGCACATGGCACCATGCCCAGTTAATTTAT CTCCCACCTCAGCCTCCTGAGTAGCTGGGACT_CAGGCACATGGCACCATGCCCAGTTAATTTAT TA T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs772570179 Functional Loss DEL dbSNP153 33..33 33 - - - 7352 RMVar_ID_7352 Human_SNP_ID_98961396 A-to-I Human chr2 + 159257216 159257216 159257216 TAGAGATGGGGTTTCACCATGTTGCCCAAGCTAATCTCAGACTCCTGGGCTCACGCAATCCATCC TAGAGATGGGGTTTCACCATGTTGCCCAAGCTGATCTCAGACTCCTGGGCTCACGCAATCCATCC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1330500306 Functional Loss SNV dbSNP153 33..33 33 - - - 7353 RMVar_ID_7353 Human_SNP_ID_98976489 A-to-I Human chr2 - 159323026 159323025 159323027 TTACCTCGCCACTGCACTCCAGCCTGGGCAACAGAGTGAGATTGTCTCAAAAAAAAAAAAAAAAG TTACCTCGCCACTGCACTCCAGCCTGGGCAA__GAGTGAGATTGTCTCAAAAAAAAAAAAAAAAG CTG C BAZ2B Ensembl:ENSG00000123636 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1464833449 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_204054 7354 RMVar_ID_7354 Human_SNP_ID_98976517 A-to-I Human chr2 - 159323131 159323131 159323131 AAAGTACAAAAATTAGCTGGGCATGGTGGTGTATGCCTGTAGTCCCAGCTACTCAGGGATGAGGC AAAGTACAAAAATTAGCTGGGCATGGTGGTGTGTGCCTGTAGTCCCAGCTACTCAGGGATGAGGC T C BAZ2B Ensembl:ENSG00000123636 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1036403052 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_204054 7355 RMVar_ID_7355 Human_SNP_ID_98976529 A-to-I Human chr2 - 159323163 159323163 159323163 CTGGCCAATATGGTGAAATCTCATCTCTACTAAAAGTACAAAAATTAGCTGGGCATGGTGGTGTA CTGGCCAATATGGTGAAATCTCATCTCTACTACAAGTACAAAAATTAGCTGGGCATGGTGGTGTA T G BAZ2B Ensembl:ENSG00000123636 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1219715573 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_204054 7356 RMVar_ID_7356 Human_SNP_ID_98976635 A-to-I Human chr2 - 159323721 159323721 159323721 CGGCTCACTGCAATCTCTGCCTCCCGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGCT CGGCTCACTGCAATCTCTGCCTCCCGGGTTCATGTGATTCTCCTGCCTCAGCCTCCCAAGTAGCT T A BAZ2B Ensembl:ENSG00000123636 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1389503922 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_204054 7357 RMVar_ID_7357 Human_SNP_ID_98976636 A-to-I Human chr2 - 159323722 159323722 159323722 TCGGCTCACTGCAATCTCTGCCTCCCGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGC TCGGCTCACTGCAATCTCTGCCTCCCGGGTTCTAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGC T A BAZ2B Ensembl:ENSG00000123636 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1036176365 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_204054 7358 RMVar_ID_7358 Human_SNP_ID_98979571 A-to-I Human chr2 - 159335051 159335051 159335051 TGATTTCTTGCCAGTTATGGTGGTGCATGCTGATAGTCCCAGCTACTCCAGAGGCCAAGGCAGGA TGATTTCTTGCCAGTTATGGTGGTGCATGCTGGTAGTCCCAGCTACTCCAGAGGCCAAGGCAGGA T C BAZ2B Ensembl:ENSG00000123636 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs925435409 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59412,RMVar_hsa_circ_72710,RMVar_hsa_circ_342698,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_27172,RMVar_hsa_circ_44448,RMVar_hsa_circ_204057,RMVar_hsa_circ_74566,RMVar_hsa_circ_204058,RMVar_hsa_circ_378608,RMVar_hsa_circ_57275,RMVar_hsa_circ_33702 7359 RMVar_ID_7359 Human_SNP_ID_98999949 A-to-I Human chr2 - 159423310 159423310 159423310 AGCCATTCTTTTGTTTGTTTGTTTGTTTAGATAGAGTCTTGCTCTGTCACCCAGGCTGGAGTGCA AGCCATTCTTTTGTTTGTTTGTTTGTTTAGATGGAGTCTTGCTCTGTCACCCAGGCTGGAGTGCA T C BAZ2B Ensembl:ENSG00000123636 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1023411159 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59412,RMVar_hsa_circ_72710,RMVar_hsa_circ_352353,RMVar_hsa_circ_36083,RMVar_hsa_circ_78584,RMVar_hsa_circ_204058,RMVar_hsa_circ_21926,RMVar_hsa_circ_69693,RMVar_hsa_circ_67314,RMVar_hsa_circ_70041,RMVar_hsa_circ_114754,RMVar_hsa_circ_349798,RMVar_hsa_circ_204070,RMVar_hsa_circ_15882,RMVar_hsa_circ_70105,RMVar_hsa_circ_15782,RMVar_hsa_circ_78347,RMVar_hsa_circ_68899,RMVar_hsa_circ_269243,RMVar_hsa_circ_204071,RMVar_hsa_circ_354040,RMVar_hsa_circ_69346,RMVar_hsa_circ_63314,RMVar_hsa_circ_13112 7360 RMVar_ID_7360 Human_SNP_ID_99002146 A-to-I Human chr2 - 159432878 159432878 159432878 CCTGCAAAATCTTTAGTGGAACAATTCAGAGGAACAGATTCAGACATTCCCAGTAGTAAAGATTC CCTGCAAAATCTTTAGTGGAACAATTCAGAGGGACAGATTCAGACATTCCCAGTAGTAAAGATTC T C BAZ2B Ensembl:ENSG00000123636 Protein coding CDS GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1453728052 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9347267,Human_RBP_ID_18748415,Human_RBP_ID_27817695 Human_miRNA_ID_2978461 RMVar_hsa_circ_59412,RMVar_hsa_circ_72710,RMVar_hsa_circ_36083,RMVar_hsa_circ_78584,RMVar_hsa_circ_204058,RMVar_hsa_circ_21926,RMVar_hsa_circ_69693,RMVar_hsa_circ_114754,RMVar_hsa_circ_349798,RMVar_hsa_circ_204070,RMVar_hsa_circ_15782,RMVar_hsa_circ_78347,RMVar_hsa_circ_204071,RMVar_hsa_circ_354040,RMVar_hsa_circ_13112,RMVar_hsa_circ_338472,RMVar_hsa_circ_355396,RMVar_hsa_circ_350686,RMVar_hsa_circ_71198,RMVar_hsa_circ_68600,RMVar_hsa_circ_60211,RMVar_hsa_circ_327641,RMVar_hsa_circ_204074,RMVar_hsa_circ_366206,RMVar_hsa_circ_204075,RMVar_hsa_circ_67363 7361 RMVar_ID_7361 Human_SNP_ID_99027359 A-to-I Human chr2 - 159542593 159542593 159542593 TTACTCTCTTGCCTGGGCTGGATTGCAGTGGTATGATCATAGCTCATGGCAGCCATGAACTCCTG TTACTCTCTTGCCTGGGCTGGATTGCAGTGGTGTGATCATAGCTCATGGCAGCCATGAACTCCTG T C BAZ2B Ensembl:ENSG00000123636 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1015257192 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72710,RMVar_hsa_circ_204084,RMVar_hsa_circ_312940,RMVar_hsa_circ_81141,RMVar_hsa_circ_204082,RMVar_hsa_circ_295892 7362 RMVar_ID_7362 Human_SNP_ID_99029239 A-to-I Human chr2 - 159551037 159551037 159551037 GCCCTGGAGTTAAAGACCAACCTGGGCAATATAGTGAGACTTTGTCTCTACAAAATAATAAACAA GCCCTGGAGTTAAAGACCAACCTGGGCAATATCGTGAGACTTTGTCTCTACAAAATAATAAACAA T G BAZ2B Ensembl:ENSG00000123636 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs999506127 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72710,RMVar_hsa_circ_204084,RMVar_hsa_circ_312940,RMVar_hsa_circ_81141,RMVar_hsa_circ_204082,RMVar_hsa_circ_295892,RMVar_hsa_circ_204085 7363 RMVar_ID_7363 Human_SNP_ID_99032903 A-to-I Human chr2 - 159566188 159566188 159566188 TGACCAACATGGAGAAACCCCATCTCTACTAAAAATACAAAATTAGCCAGACGTGGTGGTGCATG TGACCAACATGGAGAAACCCCATCTCTACTAACAATACAAAATTAGCCAGACGTGGTGGTGCATG T G BAZ2B Ensembl:ENSG00000123636 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1559790858 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72710,RMVar_hsa_circ_81141,RMVar_hsa_circ_204082,RMVar_hsa_circ_204085,RMVar_hsa_circ_204086,RMVar_hsa_circ_204087 7364 RMVar_ID_7364 Human_SNP_ID_99032904 A-to-I Human chr2 - 159566193 159566193 159566193 CAGCCTGACCAACATGGAGAAACCCCATCTCTACTAAAAATACAAAATTAGCCAGACGTGGTGGT CAGCCTGACCAACATGGAGAAACCCCATCTCTGCTAAAAATACAAAATTAGCCAGACGTGGTGGT T C BAZ2B Ensembl:ENSG00000123636 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs968779133 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72710,RMVar_hsa_circ_81141,RMVar_hsa_circ_204082,RMVar_hsa_circ_204085,RMVar_hsa_circ_204086,RMVar_hsa_circ_204087 7365 RMVar_ID_7365 Human_SNP_ID_99040809 A-to-I Human chr2 - 159598730 159598730 159598730 ACTCCTTCAGCCTCCCAAGTAGCTGGGATTACAGGTGCCTGGCTAATTTTTGTATTTTTAGTAGA ACTCCTTCAGCCTCCCAAGTAGCTGGGATTACTGGTGCCTGGCTAATTTTTGTATTTTTAGTAGA T A BAZ2B Ensembl:ENSG00000123636 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1191817390 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72710,RMVar_hsa_circ_81141,RMVar_hsa_circ_204082,RMVar_hsa_circ_204087 7366 RMVar_ID_7366 Human_SNP_ID_99042506 A-to-I Human chr2 - 159605716 159605716 159605716 TAAATTTTTATTATTATTAATTTTTTAGAGACAGGGTCTTGCTCTGTTGCCCAGACTGGACTGAA TAAATTTTTATTATTATTAATTTTTTAGAGACGGGGTCTTGCTCTGTTGCCCAGACTGGACTGAA T C BAZ2B Ensembl:ENSG00000123636 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1230152775 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13657899 RMVar_hsa_circ_72710,RMVar_hsa_circ_81141,RMVar_hsa_circ_204082,RMVar_hsa_circ_204087 7367 RMVar_ID_7367 Human_SNP_ID_99056289 A-to-I Human chr2 - 159666345 159666345 159666345 TGAGGTTGGAAGATCACCTGAGTCAGTGAGGCAGAGATTGCAGTGAGCTAAAATTGGGCCATTGC TGAGGTTGGAAGATCACCTGAGTCAGTGAGGCTGAGATTGCAGTGAGCTAAAATTGGGCCATTGC T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs779063851 Functional Loss SNV dbSNP153 33..33 33 - - - 7368 RMVar_ID_7368 Human_SNP_ID_99068528 A-to-I Human chr2 + 159715531 159715531 159715531 ACCATGTCTGACTAATTTTTATATTTTTTTATAGAGACAGTTTCACCATGTTTCCCAGGCTGGTC ACCATGTCTGACTAATTTTTATATTTTTTTATCGAGACAGTTTCACCATGTTTCCCAGGCTGGTC A C MARCHF7 Ensembl:ENSG00000136536 Protein coding intron GSE38233;GSE105773 cultured B-cells;Glioblastoma cells,U87MG - 24183664,29724793 RNA-Seq:(High) rs1327760518 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18403,RMVar_hsa_circ_99514,RMVar_hsa_circ_332572,RMVar_hsa_circ_366916,RMVar_hsa_circ_204090,RMVar_hsa_circ_339189,RMVar_hsa_circ_65907 7369 RMVar_ID_7369 Human_SNP_ID_99072529 A-to-I Human chr2 + 159730910 159730910 159730910 TGTTTTTGATTGTTTGTTTGTTTCTTTTTTTGAGACAGGATCTCACTCTGTTACCCAGGCTGGAG TGTTTTTGATTGTTTGTTTGTTTCTTTTTTTGCGACAGGATCTCACTCTGTTACCCAGGCTGGAG A C MARCHF7 Ensembl:ENSG00000136536 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs759534497 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3601160,Human_RBP_ID_6842019 RMVar_hsa_circ_204093,RMVar_hsa_circ_18403,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_302519,RMVar_hsa_circ_204092,RMVar_hsa_circ_270992,RMVar_hsa_circ_300620,RMVar_hsa_circ_339415,RMVar_hsa_circ_311898,RMVar_hsa_circ_287878,RMVar_hsa_circ_269594,RMVar_hsa_circ_204095,RMVar_hsa_circ_204096,RMVar_hsa_circ_204094 7370 RMVar_ID_7370 Human_SNP_ID_99072531 A-to-I Human chr2 + 159730914 159730914 159730914 TTTGATTGTTTGTTTGTTTCTTTTTTTGAGACAGGATCTCACTCTGTTACCCAGGCTGGAGTGAG TTTGATTGTTTGTTTGTTTCTTTTTTTGAGACCGGATCTCACTCTGTTACCCAGGCTGGAGTGAG A C MARCHF7 Ensembl:ENSG00000136536 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs769121659 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3601160 RMVar_hsa_circ_204093,RMVar_hsa_circ_18403,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_302519,RMVar_hsa_circ_204092,RMVar_hsa_circ_270992,RMVar_hsa_circ_300620,RMVar_hsa_circ_339415,RMVar_hsa_circ_311898,RMVar_hsa_circ_287878,RMVar_hsa_circ_269594,RMVar_hsa_circ_204095,RMVar_hsa_circ_204096,RMVar_hsa_circ_204094 7371 RMVar_ID_7371 Human_SNP_ID_99072555 A-to-I Human chr2 + 159730967 159730967 159730967 GGCTGGAGTGAGTGGTGCAATCACGGCTCACTACAGCCTAGACCTCCCAGGCTCAAGTGGTCCTC GGCTGGAGTGAGTGGTGCAATCACGGCTCACTGCAGCCTAGACCTCCCAGGCTCAAGTGGTCCTC A G MARCHF7 Ensembl:ENSG00000136536 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1443304249 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1297973,Human_RBP_ID_25476001 RMVar_hsa_circ_204093,RMVar_hsa_circ_18403,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_302519,RMVar_hsa_circ_204092,RMVar_hsa_circ_270992,RMVar_hsa_circ_300620,RMVar_hsa_circ_339415,RMVar_hsa_circ_311898,RMVar_hsa_circ_287878,RMVar_hsa_circ_269594,RMVar_hsa_circ_204095,RMVar_hsa_circ_204096,RMVar_hsa_circ_204094 7372 RMVar_ID_7372 Human_SNP_ID_99072565 A-to-I Human chr2 + 159731026 159731026 159731026 GTCCTCTCACCTCAGCCTCTCCTCCAGCAGCTAGGACTGCAGGGACGTGCCACCATGCCTAGCTA GTCCTCTCACCTCAGCCTCTCCTCCAGCAGCTGGGACTGCAGGGACGTGCCACCATGCCTAGCTA A G MARCHF7 Ensembl:ENSG00000136536 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1407713084 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6842020 RMVar_hsa_circ_204093,RMVar_hsa_circ_18403,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_302519,RMVar_hsa_circ_204092,RMVar_hsa_circ_270992,RMVar_hsa_circ_300620,RMVar_hsa_circ_339415,RMVar_hsa_circ_311898,RMVar_hsa_circ_287878,RMVar_hsa_circ_269594,RMVar_hsa_circ_204095,RMVar_hsa_circ_204096,RMVar_hsa_circ_204094 7373 RMVar_ID_7373 Human_SNP_ID_99076491 A-to-I Human chr2 + 159745516 159745516 159745516 ATCTTCACTAAAAATACAAAAATTAGCCGGGCATGGTGGCACGCGCCTTGTAGTCCCAGATATTC ATCTTCACTAAAAATACAAAAATTAGCCGGGCGTGGTGGCACGCGCCTTGTAGTCCCAGATATTC A G MARCHF7 Ensembl:ENSG00000136536 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs767883231 Functional Loss SNV dbSNP153 33..33 33 - - - 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 7374 RMVar_ID_7374 Human_SNP_ID_99082997 A-to-I Human chr2 - 159770082 159770082 159770082 TGTGAACTAAAAGAGTTCTAAAGGAGTTCTTAAAGGAGTGGTAGAATTTGGGTAGGAAAGTGATT TGTGAACTAAAAGAGTTCTAAAGGAGTTCTTAGAGGAGTGGTAGAATTTGGGTAGGAAAGTGATT T C CD302 Ensembl:ENSG00000241399 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11702 Functional Loss SNV dbSNP153 33..33 33 - - - 7375 RMVar_ID_7375 Human_SNP_ID_99082998 A-to-I Human chr2 - 159770083 159770083 159770083 ATGTGAACTAAAAGAGTTCTAAAGGAGTTCTTAAAGGAGTGGTAGAATTTGGGTAGGAAAGTGAT ATGTGAACTAAAAGAGTTCTAAAGGAGTTCTTCAAGGAGTGGTAGAATTTGGGTAGGAAAGTGAT T G CD302 Ensembl:ENSG00000241399 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1254649722 Functional Loss SNV dbSNP153 33..33 33 - - - 7376 RMVar_ID_7376 Human_SNP_ID_99099738 A-to-I Human chr2 - 159838858 159838858 159838858 CTGGGAGGTGGAGGTTGCAGTGAGCCGAGATTATACCACTGCATTCCAGCCTGGGCGACAGAGTG CTGGGAGGTGGAGGTTGCAGTGAGCCGAGATTCTACCACTGCATTCCAGCCTGGGCGACAGAGTG T G LY75-CD302,LY75 Ensembl:ENSG00000248672,Ensembl:ENSG00000054219 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1286586678 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_371112,RMVar_hsa_circ_204118 7377 RMVar_ID_7377 Human_SNP_ID_99099914 A-to-I Human chr2 - 159839677 159839677 159839677 CATCAGCAGCATGGCTGGGCACCGTGGTGCACACCCGTAGTCCCATTTACTCTGGAGGCAAGAGG CATCAGCAGCATGGCTGGGCACCGTGGTGCACGCCCGTAGTCCCATTTACTCTGGAGGCAAGAGG T C LY75-CD302,LY75 Ensembl:ENSG00000248672,Ensembl:ENSG00000054219 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs968386643 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_371112,RMVar_hsa_circ_204118 7378 RMVar_ID_7378 Human_SNP_ID_99100127 A-to-I Human chr2 - 159840387 159840387 159840387 TTGTATTTTTTGTAAAGATGAGGTTTTGCCATATTGCCCAAGCTGGTCTCAAATGCCTAGACTCA TTGTATTTTTTGTAAAGATGAGGTTTTGCCATTTTGCCCAAGCTGGTCTCAAATGCCTAGACTCA T A LY75-CD302,LY75 Ensembl:ENSG00000248672,Ensembl:ENSG00000054219 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1055068954 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_371112,RMVar_hsa_circ_204118 7379 RMVar_ID_7379 Human_SNP_ID_99100129 A-to-I Human chr2 - 159840389 159840389 159840389 TTTTGTATTTTTTGTAAAGATGAGGTTTTGCCATATTGCCCAAGCTGGTCTCAAATGCCTAGACT TTTTGTATTTTTTGTAAAGATGAGGTTTTGCCGTATTGCCCAAGCTGGTCTCAAATGCCTAGACT T C LY75-CD302,LY75 Ensembl:ENSG00000248672,Ensembl:ENSG00000054219 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1326553612 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_371112,RMVar_hsa_circ_204118 7380 RMVar_ID_7380 Human_SNP_ID_99100163 A-to-I Human chr2 - 159840515 159840515 159840515 CAGGCTGGAGTACAGTGGTGTGATCACACTTCACTGCAGCCTTGACCTCCCGGGCTCAAGCGATC CAGGCTGGAGTACAGTGGTGTGATCACACTTCTCTGCAGCCTTGACCTCCCGGGCTCAAGCGATC T A LY75-CD302,LY75 Ensembl:ENSG00000248672,Ensembl:ENSG00000054219 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs945600704 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_371112,RMVar_hsa_circ_204118 7381 RMVar_ID_7381 Human_SNP_ID_99106385 A-to-I Human chr2 - 159866912 159866912 159866912 TAGAAAGTTGAGGATGAACCTCTAAAAAGGCTACCAGTGGGAGCCTCTACAATGCAGGTGACAAA TAGAAAGTTGAGGATGAACCTCTAAAAAGGCTGCCAGTGGGAGCCTCTACAATGCAGGTGACAAA T C LY75-CD302,LY75 Ensembl:ENSG00000248672,Ensembl:ENSG00000054219 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2729721 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_432,GWAS_ID_433 RMVar_hsa_circ_45719 7382 RMVar_ID_7382 Human_SNP_ID_99107151 A-to-I Human chr2 - 159870329 159870329 159870329 CCCCCACTTCAGCCTCCCAAGTAGCTGGGACTACAATCACATGCCACCACACCCAGCTAATGTTT CCCCCACTTCAGCCTCCCAAGTAGCTGGGACTGCAATCACATGCCACCACACCCAGCTAATGTTT T C LY75-CD302,LY75 Ensembl:ENSG00000248672,Ensembl:ENSG00000054219 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1401224614 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45719 7383 RMVar_ID_7383 Human_SNP_ID_99107472 A-to-I Human chr2 - 159871721 159871712 159871722 CAGGTGATCTGCCCACCTCAGCCTCCCAAAGTACTGGGATTACAGGCATTAGCCACCACACCCAG CAGGTGATCTGCCCACCTCAGCCTCCCAAAG__________ACAGGCATTAGCCACCACACCCAG TAATCCCAGTA T LY75-CD302,LY75 Ensembl:ENSG00000248672,Ensembl:ENSG00000054219 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1313805578 Functional Loss DEL dbSNP153 32..41 33 - - - RMVar_hsa_circ_45719 7384 RMVar_ID_7384 Human_SNP_ID_99107474 A-to-I Human chr2 - 159871721 159871721 159871721 CAGGTGATCTGCCCACCTCAGCCTCCCAAAGTACTGGGATTACAGGCATTAGCCACCACACCCAG CAGGTGATCTGCCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATTAGCCACCACACCCAG T C LY75-CD302,LY75 Ensembl:ENSG00000248672,Ensembl:ENSG00000054219 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1038969897 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45719 7385 RMVar_ID_7385 Human_SNP_ID_99107478 A-to-I Human chr2 - 159871734 159871734 159871734 GAACTTCTGACCTCAGGTGATCTGCCCACCTCAGCCTCCCAAAGTACTGGGATTACAGGCATTAG GAACTTCTGACCTCAGGTGATCTGCCCACCTCGGCCTCCCAAAGTACTGGGATTACAGGCATTAG T C LY75-CD302,LY75 Ensembl:ENSG00000248672,Ensembl:ENSG00000054219 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs890412203 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45719 7386 RMVar_ID_7386 Human_SNP_ID_99122832 A-to-I Human chr2 - 159936220 159936220 159936220 GGCTGGGCGCGGTGGCTCACGCCTGTAATCCCAGCAACTTTGGGAGGCCGAGGCGGGTGGATCAC GGCTGGGCGCGGTGGCTCACGCCTGTAATCCCGGCAACTTTGGGAGGCCGAGGCGGGTGGATCAC T C PLA2R1 Ensembl:ENSG00000153246 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1044758708 Functional Loss SNV dbSNP153 33..33 33 - - - 7387 RMVar_ID_7387 Human_SNP_ID_99177619 A-to-I Human chr2 - 160163427 160163427 160163427 GGGTTTCACCATGTTGGCCAGACTGGTCTCGAACTCCTGATCTCAAATGATCCACCCACCTCGAC GGGTTTCACCATGTTGGCCAGACTGGTCTCGATCTCCTGATCTCAAATGATCCACCCACCTCGAC T A ITGB6,AC092153.1 Ensembl:ENSG00000115221,Ensembl:ENSG00000285155 Protein coding,lincRNA intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs920839780 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84964,RMVar_hsa_circ_106503,RMVar_hsa_circ_101857,RMVar_hsa_circ_204123,RMVar_hsa_circ_204125,RMVar_hsa_circ_66696,RMVar_hsa_circ_204126 7388 RMVar_ID_7388 Human_SNP_ID_99241010 A-to-I Human chr2 - 160431130 160431130 160431130 AGTCTAATTTTATTAGACTATTTTATTAGACTATTGCCTAGGTAACCCAGGCCATTCTTGGATTC AGTCTAATTTTATTAGACTATTTTATTAGACTGTTGCCTAGGTAACCCAGGCCATTCTTGGATTC T C RBMS1 Ensembl:ENSG00000153250 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1266064636 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1320 7389 RMVar_ID_7389 Human_SNP_ID_99453919 A-to-I Human chr2 + 161322573 161322573 161322573 CTCCACGCCCAGCTAATTTTTTTATTTTTAGTAGAGGTGGGGTTTCACCAAGTTGGCCGGGCTGG CTCCACGCCCAGCTAATTTTTTTATTTTTAGTGGAGGTGGGGTTTCACCAAGTTGGCCGGGCTGG A G PSMD14 Ensembl:ENSG00000115233 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs746931069 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13661040 RMVar_hsa_circ_75435,RMVar_hsa_circ_364499 7390 RMVar_ID_7390 Human_SNP_ID_99458097 A-to-I Human chr2 - 161341220 161341220 161341220 ACTGGTGCGGCGTGGGGCGGCCGCGAGCCCGGAGCCTGCCCGCGCGCCCCCGGAACCCGCGCCCC ACTGGTGCGGCGTGGGGCGGCCGCGAGCCCGGGGCCTGCCCGCGCGCCCCCGGAACCCGCGCCCC T C MXRA7P1 Ensembl:ENSG00000232320 Pseudogene exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1413497495 Functional Loss SNV dbSNP153 33..33 33 - - - 7391 RMVar_ID_7391 Human_SNP_ID_99682176 A-to-I Human chr2 - 162263333 162263333 162263333 AAAAACGTGATATTTGTTGACACCTCAAAAACAGTCTACATAAGTTACAGTAGTACAAAATAGAA AAAAACGTGATATTTGTTGACACCTCAAAAACGGTCTACATAAGTTACAGTAGTACAAAATAGAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1390622320 Functional Loss SNV dbSNP153 33..33 33 - - - 7392 RMVar_ID_7392 Human_SNP_ID_100270196 A-to-I Human chr2 - 164707320 164707320 164707320 CCTAGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCCAGGTGTCATATTGC CCTAGCCAACATGGTGAAACCCCATCTCTACTGAAAATACAAAAATTAGCCAGGTGTCATATTGC T C COBLL1 Ensembl:ENSG00000082438 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054831901 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39680,RMVar_hsa_circ_364897,RMVar_hsa_circ_341025,RMVar_hsa_circ_328563,RMVar_hsa_circ_57967,RMVar_hsa_circ_204253,RMVar_hsa_circ_67546,RMVar_hsa_circ_63442,RMVar_hsa_circ_64521,RMVar_hsa_circ_62460,RMVar_hsa_circ_63142 7393 RMVar_ID_7393 Human_SNP_ID_100324951 A-to-I Human chr2 - 164947301 164947301 164947301 GTGGCAAAACCCCGTCTCTGCTAAAAATACAAAAATTAGCCAGGCATGGTGGTGGGCACCTGCAA GTGGCAAAACCCCGTCTCTGCTAAAAATACAAGAATTAGCCAGGCATGGTGGTGGGCACCTGCAA T C SLC38A11 Ensembl:ENSG00000169507 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1183029270 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22184,RMVar_hsa_circ_53481,RMVar_hsa_circ_55499 7394 RMVar_ID_7394 Human_SNP_ID_290423723 A-to-I Human chr6 - 105100320 105100320 105100320 TATTTTTAGTAGAGATGGGGTTTCACTGTGTTAGCCAGGATGGTCTCGATCTCCTGACCTCGTGA TATTTTTAGTAGAGATGGGGTTTCACTGTGTTGGCCAGGATGGTCTCGATCTCCTGACCTCGTGA T C BVES Ensembl:ENSG00000112276 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs369491691 Functional Loss SNV dbSNP153 33..33 33 - - - 7395 RMVar_ID_7395 Human_SNP_ID_290680282 A-to-I Human chr6 - 106198719 106198719 106198719 CAGGTTGGAGCGCAGTGGTGCAATCTTGGCTAACTGCAACCTCCACCTCCGGGTTCAAGTGATTC CAGGTTGGAGCGCAGTGGTGCAATCTTGGCTAGCTGCAACCTCCACCTCCGGGTTCAAGTGATTC T C ATG5 Ensembl:ENSG00000057663 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs752473495 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15583838 7396 RMVar_ID_7396 Human_SNP_ID_290780259 A-to-I Human chr6 - 106609363 106609363 106609363 TTTCGTAGAGATGTGATCTCATGATGTTGCCCAGGCTGATCTTCAACTCCTGGGCTCAAGCAATC TTTCGTAGAGATGTGATCTCATGATGTTGCCCGGGCTGATCTTCAACTCCTGGGCTCAAGCAATC T C RTN4IP1 Ensembl:ENSG00000130347 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1273733043 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_308896,RMVar_hsa_circ_374041,RMVar_hsa_circ_240694,RMVar_hsa_circ_240696,RMVar_hsa_circ_329411 7397 RMVar_ID_7397 Human_SNP_ID_290788759 A-to-I Human chr6 + 106643965 106643965 106643965 GCGATCTCGGCTCGCTGCAGCCTCCGCCTCCCAGCTTCAAGCGATTCTCCTGACTCAGCCTCCCA GCGATCTCGGCTCGCTGCAGCCTCCGCCTCCCGGCTTCAAGCGATTCTCCTGACTCAGCCTCCCA A G QRSL1 Ensembl:ENSG00000130348 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1319165357 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13324,RMVar_hsa_circ_272784,RMVar_hsa_circ_67402,RMVar_hsa_circ_62321,RMVar_hsa_circ_40693,RMVar_hsa_circ_72464,RMVar_hsa_circ_72492 7398 RMVar_ID_7398 Human_SNP_ID_290793936 A-to-I Human chr6 + 106666058 106666051 106666058 CTTTTAGGCTGGGTGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGAGCGG CTTTTAGGCTGGGTGCAGTGGCTCAC_______ATCCCAGCACTTTGGGAGGCCAAGGCGAGCGG CACCTGTA C QRSL1 Ensembl:ENSG00000130348 Protein coding 3'UTR GSE38233;GSE100210;GSE99789 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 24183664,29129909,29796672 RNA-Seq:(High) rs1562174278 Functional Loss DEL dbSNP153 27..33 33 - - - 7399 RMVar_ID_7399 Human_SNP_ID_290794392 A-to-I Human chr6 + 106668008 106668008 106668008 GAGAGATGGGCTCTCCCTGTGTTGCCCAGGCTAGTCTCAAACTCCTGGGCTCAAGTGATCTGCCT GAGAGATGGGCTCTCCCTGTGTTGCCCAGGCTGGTCTCAAACTCCTGGGCTCAAGTGATCTGCCT A G QRSL1 Ensembl:ENSG00000130348 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1226130458 Functional Loss SNV dbSNP153 33..33 33 - - - 7400 RMVar_ID_7400 Human_SNP_ID_290881870 A-to-I Human chr6 + 107035295 107035295 107035295 AGCTGGGATTACAGGCACGCACCACCATGCCCAGCTAATTTTGTATTTTTAGCAGAGACCGGGTT AGCTGGGATTACAGGCACGCACCACCATGCCCGGCTAATTTTGTATTTTTAGCAGAGACCGGGTT A G MTRES1 Ensembl:ENSG00000130349 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1316319102 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_367028 7401 RMVar_ID_7401 Human_SNP_ID_290881890 A-to-I Human chr6 + 107035381 107035381 107035381 AAACTCCCAAACTCAGGTCATCAGTCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAG AAACTCCCAAACTCAGGTCATCAGTCCACCTCTGCCTCCCAAAGTGCTGGGATTACAGGCATGAG A T MTRES1 Ensembl:ENSG00000130349 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1362983330 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_367028 7402 RMVar_ID_7402 Human_SNP_ID_290882936 A-to-I Human chr6 + 107039572 107039572 107039572 GTACTCCTGACCTCAGGTGATCCACCCACCTCAGCCTCCCAAAGTGCTGAGATTACAGGCGTGAA GTACTCCTGACCTCAGGTGATCCACCCACCTCGGCCTCCCAAAGTGCTGAGATTACAGGCGTGAA A G MTRES1 Ensembl:ENSG00000130349 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1554227328 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_367028 7403 RMVar_ID_7403 Human_SNP_ID_290883316 A-to-I Human chr6 + 107040748 107040748 107040748 AAAATTAGCCGGGCGAGGTGGCAGGCGCCTGTAGTCCCAGCTGCTTGAGAGGCTGAGGCAGGAGA AAAATTAGCCGGGCGAGGTGGCAGGCGCCTGTTGTCCCAGCTGCTTGAGAGGCTGAGGCAGGAGA A T MTRES1 Ensembl:ENSG00000130349 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs943129077 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_240701,RMVar_hsa_circ_367028,RMVar_hsa_circ_300689 7404 RMVar_ID_7404 Human_SNP_ID_290883402 A-to-I Human chr6 + 107040955 107040955 107040955 GTTGGTTAAGAATGCACGCTTTGGCTGGGCGCAGTGGCTCATGTCTGTAATCCGAGCACTTTGGG GTTGGTTAAGAATGCACGCTTTGGCTGGGCGCGGTGGCTCATGTCTGTAATCCGAGCACTTTGGG A G MTRES1 Ensembl:ENSG00000130349 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs189803927 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_240701,RMVar_hsa_circ_367028,RMVar_hsa_circ_300689 7405 RMVar_ID_7405 Human_SNP_ID_290883409 A-to-I Human chr6 + 107040971 107040971 107040971 CGCTTTGGCTGGGCGCAGTGGCTCATGTCTGTAATCCGAGCACTTTGGGAGGCCAAGGCGGGCGG CGCTTTGGCTGGGCGCAGTGGCTCATGTCTGTGATCCGAGCACTTTGGGAGGCCAAGGCGGGCGG A G MTRES1 Ensembl:ENSG00000130349 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1168657984 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_240701,RMVar_hsa_circ_367028,RMVar_hsa_circ_300689 7406 RMVar_ID_7406 Human_SNP_ID_290883427 A-to-I Human chr6 + 107041009 107041009 107041009 AGCACTTTGGGAGGCCAAGGCGGGCGGATCACAAGGTCAGGAGATCGAGACCATCCTGGCTAGCA AGCACTTTGGGAGGCCAAGGCGGGCGGATCACGAGGTCAGGAGATCGAGACCATCCTGGCTAGCA A G MTRES1 Ensembl:ENSG00000130349 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs62429963 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_240701,RMVar_hsa_circ_367028,RMVar_hsa_circ_300689 7407 RMVar_ID_7407 Human_SNP_ID_290883693 A-to-I Human chr6 + 107041655 107041655 107041655 TCACGCCATTCTCCTGCCTCAGCCTCCCGAGTAGTTGGGAATACAGGCGCCCACCACCACGCCTG TCACGCCATTCTCCTGCCTCAGCCTCCCGAGTTGTTGGGAATACAGGCGCCCACCACCACGCCTG A T MTRES1 Ensembl:ENSG00000130349 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968539407 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_240701,RMVar_hsa_circ_367028,RMVar_hsa_circ_300689 7408 RMVar_ID_7408 Human_SNP_ID_290883737 A-to-I Human chr6 + 107041801 107041801 107041801 CCACCCACCTCCGCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCCTGGCGAAGATTT CCACCCACCTCCGCTCCCAAAGTGCTGGGATTGCAGGCGTGAGCCACCGCGCCTGGCGAAGATTT A G MTRES1 Ensembl:ENSG00000130349 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1554227817 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26539610 RMVar_hsa_circ_240701,RMVar_hsa_circ_367028,RMVar_hsa_circ_300689 7409 RMVar_ID_7409 Human_SNP_ID_290896276 A-to-I Human chr6 - 107086612 107086612 107086612 CTCCAGTCCTGGATTTGGTCTGTCTTTTTTTTAAGACGGAGTCTTGCTCTGTCTCTGGCCAGAGT CTCCAGTCCTGGATTTGGTCTGTCTTTTTTTTTAGACGGAGTCTTGCTCTGTCTCTGGCCAGAGT T A BEND3 Ensembl:ENSG00000178409 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1554234311 Functional Loss SNV dbSNP153 33..33 33 - - - 7410 RMVar_ID_7410 Human_SNP_ID_290903257 A-to-I Human chr6 - 107113138 107113138 107113138 GTGCTTTTTTTTTTTAGACAGAGTCTCGCTCTATCACCAGGCTGTAGTGCAGTGGCGTGATCTCT GTGCTTTTTTTTTTTAGACAGAGTCTCGCTCTGTCACCAGGCTGTAGTGCAGTGGCGTGATCTCT T C BEND3 Ensembl:ENSG00000178409 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1293348072 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15585892 7411 RMVar_ID_7411 Human_SNP_ID_290914280 A-to-I Human chr6 - 107153390 107153389 107153390 AAATTTTGGTCTTGAACCACAGACATCCAATTACAGAAAGAATATAAGCAATCTCACAGGCCTGC AAATTTTGGTCTTGAACCACAGACATCCAATT_CAGAAAGAATATAAGCAATCTCACAGGCCTGC GT G PDSS2 Ensembl:ENSG00000164494 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1256062426 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_18059505,Human_RBP_ID_18363478 RMVar_hsa_circ_84083,RMVar_hsa_circ_240703 7412 RMVar_ID_7412 Human_SNP_ID_290919658 A-to-I Human chr6 - 107175040 107175040 107175040 GCCTGGCTAATTTTTGTATTTTTAGTAGAAACAGGTTTCACCATGTTGGCCAGGCTGGTCTTGAA GCCTGGCTAATTTTTGTATTTTTAGTAGAAACGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAA T C PDSS2 Ensembl:ENSG00000164494 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs894378612 Functional Loss SNV dbSNP153 33..33 33 - - - 7413 RMVar_ID_7413 Human_SNP_ID_290919878 A-to-I Human chr6 - 107176180 107176180 107176180 AAAATTAGCTGAGTGTGGTGGCGCTTACCTATAATCCCAGCTACTGGGGAGGCTGAGGCAGAAGA AAAATTAGCTGAGTGTGGTGGCGCTTACCTATGATCCCAGCTACTGGGGAGGCTGAGGCAGAAGA T C PDSS2 Ensembl:ENSG00000164494 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs372392205 Functional Loss SNV dbSNP153 33..33 33 - - - 7414 RMVar_ID_7414 Human_SNP_ID_290922573 A-to-I Human chr6 - 107188186 107188186 107188186 TTTTGTAGAGATGGGGTTTTACCACATTGCTCAGGCTGGTCTCGAACTCCTGAACTCAAAGCGAT TTTTGTAGAGATGGGGTTTTACCACATTGCTCGGGCTGGTCTCGAACTCCTGAACTCAAAGCGAT T C PDSS2 Ensembl:ENSG00000164494 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1050225409 Functional Loss SNV dbSNP153 33..33 33 - - - 7415 RMVar_ID_7415 Human_SNP_ID_290922574 A-to-I Human chr6 - 107188193 107188193 107188193 TTGTATTTTTTGTAGAGATGGGGTTTTACCACATTGCTCAGGCTGGTCTCGAACTCCTGAACTCA TTGTATTTTTTGTAGAGATGGGGTTTTACCACCTTGCTCAGGCTGGTCTCGAACTCCTGAACTCA T G PDSS2 Ensembl:ENSG00000164494 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1447671795 Functional Loss SNV dbSNP153 33..33 33 - - - 7416 RMVar_ID_7416 Human_SNP_ID_290933265 A-to-I Human chr6 - 107233595 107233595 107233595 GTTGCCCGGGCTGGTCTGGAACTCCTGGCCTCAGGTGATCCTCCCATCTCAGCCTCCCAAAGCAC GTTGCCCGGGCTGGTCTGGAACTCCTGGCCTCGGGTGATCCTCCCATCTCAGCCTCCCAAAGCAC T C PDSS2 Ensembl:ENSG00000164494 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1452645390 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16387,RMVar_hsa_circ_360236,RMVar_hsa_circ_365982 7417 RMVar_ID_7417 Human_SNP_ID_290942105 A-to-I Human chr6 - 107272864 107272864 107272864 AGCCTCAAACTCCTGGGCTCAAGCGATCTCTTACCTCAGCCTCCTGAGTAGCTGGCTGGCTAATT AGCCTCAAACTCCTGGGCTCAAGCGATCTCTTTCCTCAGCCTCCTGAGTAGCTGGCTGGCTAATT T A PDSS2 Ensembl:ENSG00000164494 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1386678277 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16387,RMVar_hsa_circ_107221,RMVar_hsa_circ_108302,RMVar_hsa_circ_365907,RMVar_hsa_circ_240708,RMVar_hsa_circ_240709 7418 RMVar_ID_7418 Human_SNP_ID_290973375 A-to-I Human chr6 - 107413412 107413412 107413412 CCCACCTCAGCCTCCCAGGTAGCTGGGACTACAGGCATGTACCACAATGCCTGGCTAAATTTCTT CCCACCTCAGCCTCCCAGGTAGCTGGGACTACCGGCATGTACCACAATGCCTGGCTAAATTTCTT T G PDSS2 Ensembl:ENSG00000164494 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1219419233 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107221,RMVar_hsa_circ_240709 7419 RMVar_ID_7419 Human_SNP_ID_290975746 A-to-I Human chr6 - 107424182 107424182 107424182 AAGAAATTAGCCGGATGTGGTAATGCTCGCCTATGGTCCCAGTTACTTGAGATGCTGTCATGGGA AAGAAATTAGCCGGATGTGGTAATGCTCGCCTGTGGTCCCAGTTACTTGAGATGCTGTCATGGGA T C PDSS2 Ensembl:ENSG00000164494 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs531478894 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15587108 RMVar_hsa_circ_107221,RMVar_hsa_circ_240709 7420 RMVar_ID_7420 Human_SNP_ID_290979971 A-to-I Human chr6 - 107442365 107442365 107442365 TTGCCCAGGCTGGAGTGCAGTGGTGTGATCTCAGCTCAGTGCGACCTCTGCCTCCTGGATTCGAG TTGCCCAGGCTGGAGTGCAGTGGTGTGATCTCGGCTCAGTGCGACCTCTGCCTCCTGGATTCGAG T C PDSS2 Ensembl:ENSG00000164494 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1353917094 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107221,RMVar_hsa_circ_240709 7421 RMVar_ID_7421 Human_SNP_ID_290983130 A-to-I Human chr6 - 107455736 107455736 107455736 TTTTTTTTTTTTTTGAGACAGAGTCTCGCTCTATCGCCAGGCTGGAGTGCCCAGTGGCCTGATCT TTTTTTTTTTTTTTGAGACAGAGTCTCGCTCTGTCGCCAGGCTGGAGTGCCCAGTGGCCTGATCT T C PDSS2 Ensembl:ENSG00000164494 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs555061146 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107221,RMVar_hsa_circ_240709 7422 RMVar_ID_7422 Human_SNP_ID_290983796 A-to-I Human chr6 - 107458296 107458295 107458296 TATTTTTAGTAGATACGGGGTTTCACCGTGTTAGCCAGGATCGTCTCAATCTCCTGACCTCGTGA TATTTTTAGTAGATACGGGGTTTCACCGTGTT_GCCAGGATCGTCTCAATCTCCTGACCTCGTGA CT C PDSS2 Ensembl:ENSG00000164494 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1361925202 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_107221,RMVar_hsa_circ_240709 7423 RMVar_ID_7423 Human_SNP_ID_290995661 A-to-I Human chr6 + 107507370 107507370 107507370 TCTTCTCACCCAGGCTGGAGAGCAGTGGTGCTATCTTGGCTCACTGCAACCTCTGCCTCCCGAGT TCTTCTCACCCAGGCTGGAGAGCAGTGGTGCTGTCTTGGCTCACTGCAACCTCTGCCTCCCGAGT A G SOBP Ensembl:ENSG00000112320 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs761706288 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_240713,RMVar_hsa_circ_240715,RMVar_hsa_circ_291569,RMVar_hsa_circ_275203,RMVar_hsa_circ_240714,RMVar_hsa_circ_47756,RMVar_hsa_circ_28499 7424 RMVar_ID_7424 Human_SNP_ID_290997157 A-to-I Human chr6 + 107513943 107513943 107513943 AATTTTCACAACTCTTTGTGGATGCTATTATTAACCTTGTTTTACAGATGAGAAAACTGAGGCCC AATTTTCACAACTCTTTGTGGATGCTATTATTTACCTTGTTTTACAGATGAGAAAACTGAGGCCC A T SOBP Ensembl:ENSG00000112320 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs891437418 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_240713,RMVar_hsa_circ_240715,RMVar_hsa_circ_291569,RMVar_hsa_circ_275203,RMVar_hsa_circ_240714,RMVar_hsa_circ_47756,RMVar_hsa_circ_28499 7425 RMVar_ID_7425 Human_SNP_ID_290999163 A-to-I Human chr6 + 107522727 107522727 107522727 ATCATGCCCAGCTAATTTTTGTATTTTTTTGTAGAGATGGTGTTTCACCATGTTGCCCAGGCTGG ATCATGCCCAGCTAATTTTTGTATTTTTTTGTGGAGATGGTGTTTCACCATGTTGCCCAGGCTGG A G SOBP Ensembl:ENSG00000112320 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1159002370 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_240715,RMVar_hsa_circ_291569,RMVar_hsa_circ_275203,RMVar_hsa_circ_240714,RMVar_hsa_circ_47756,RMVar_hsa_circ_28499 7426 RMVar_ID_7426 Human_SNP_ID_291044098 A-to-I Human chr6 - 107717743 107717743 107717743 AGGAGTTTGAGACCAGCCTGACCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAGATTAG AGGAGTTTGAGACCAGCCTGACCAACATGGTGCAACCCCGTCTCTACTAAAAATACAAAGATTAG T G SCML4 Ensembl:ENSG00000146285 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1200811470 Functional Loss SNV dbSNP153 33..33 33 - - - 7427 RMVar_ID_7427 Human_SNP_ID_291083146 A-to-I Human chr6 - 107877572 107877572 107877572 GCCAGACGTGGTGCATGCCTGTAGTCTCAGCTACTTGGGAAGCTGAGGTGGGAGGATCACTTGAG GCCAGACGTGGTGCATGCCTGTAGTCTCAGCTGCTTGGGAAGCTGAGGTGGGAGGATCACTTGAG T C SEC63 Ensembl:ENSG00000025796 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs149758039 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12467,RMVar_hsa_circ_48741,RMVar_hsa_circ_59053,RMVar_hsa_circ_378651,RMVar_hsa_circ_266285,RMVar_hsa_circ_278169,RMVar_hsa_circ_320968,RMVar_hsa_circ_378111,RMVar_hsa_circ_268737,RMVar_hsa_circ_35889,RMVar_hsa_circ_40943,RMVar_hsa_circ_16249 7428 RMVar_ID_7428 Human_SNP_ID_291093737 A-to-I Human chr6 - 107918503 107918503 107918503 ATTTTTAGTAGAGACAGGGTTTTATGTTGGTCAGGCTAGTCTTGAACTCCTGACCTCAGGTGATC ATTTTTAGTAGAGACAGGGTTTTATGTTGGTCCGGCTAGTCTTGAACTCCTGACCTCAGGTGATC T G SEC63 Ensembl:ENSG00000025796 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1159068338 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15589664 RMVar_hsa_circ_173,RMVar_hsa_circ_48741,RMVar_hsa_circ_320968,RMVar_hsa_circ_35889,RMVar_hsa_circ_286430,RMVar_hsa_circ_325358,RMVar_hsa_circ_336658,RMVar_hsa_circ_240722,RMVar_hsa_circ_313956,RMVar_hsa_circ_240723,RMVar_hsa_circ_240724,RMVar_hsa_circ_80125,RMVar_hsa_circ_240727,RMVar_hsa_circ_307172,RMVar_hsa_circ_345929,RMVar_hsa_circ_276293,RMVar_hsa_circ_240728,RMVar_hsa_circ_362460,RMVar_hsa_circ_240730,RMVar_hsa_circ_89451,RMVar_hsa_circ_285183,RMVar_hsa_circ_240731,RMVar_hsa_circ_362975,RMVar_hsa_circ_240734,RMVar_hsa_circ_38924,RMVar_hsa_circ_350170,RMVar_hsa_circ_240735,RMVar_hsa_circ_240736,RMVar_hsa_circ_10920,RMVar_hsa_circ_335360,RMVar_hsa_circ_240741,RMVar_hsa_circ_282163,RMVar_hsa_circ_240740,RMVar_hsa_circ_240739,RMVar_hsa_circ_339507,RMVar_hsa_circ_314609,RMVar_hsa_circ_240743,RMVar_hsa_circ_240742,RMVar_hsa_circ_62630,RMVar_hsa_circ_5963,RMVar_hsa_circ_73169,RMVar_hsa_circ_282930,RMVar_hsa_circ_240745,RMVar_hsa_circ_374614,RMVar_hsa_circ_240746 7429 RMVar_ID_7429 Human_SNP_ID_291093955 A-to-I Human chr6 - 107919197 107919197 107919197 AAGGTTGAAATCAACTTCTGGCCAGGCGCGGTAGCTCATGCCTGTAATCCCAGCACTTTGGGAGG AAGGTTGAAATCAACTTCTGGCCAGGCGCGGTTGCTCATGCCTGTAATCCCAGCACTTTGGGAGG T A SEC63 Ensembl:ENSG00000025796 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs936772182 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_173,RMVar_hsa_circ_48741,RMVar_hsa_circ_320968,RMVar_hsa_circ_35889,RMVar_hsa_circ_286430,RMVar_hsa_circ_325358,RMVar_hsa_circ_336658,RMVar_hsa_circ_240722,RMVar_hsa_circ_313956,RMVar_hsa_circ_240723,RMVar_hsa_circ_240724,RMVar_hsa_circ_80125,RMVar_hsa_circ_240727,RMVar_hsa_circ_307172,RMVar_hsa_circ_345929,RMVar_hsa_circ_276293,RMVar_hsa_circ_240728,RMVar_hsa_circ_362460,RMVar_hsa_circ_240730,RMVar_hsa_circ_89451,RMVar_hsa_circ_285183,RMVar_hsa_circ_240731,RMVar_hsa_circ_362975,RMVar_hsa_circ_240734,RMVar_hsa_circ_38924,RMVar_hsa_circ_350170,RMVar_hsa_circ_240735,RMVar_hsa_circ_240736,RMVar_hsa_circ_10920,RMVar_hsa_circ_335360,RMVar_hsa_circ_240741,RMVar_hsa_circ_282163,RMVar_hsa_circ_240740,RMVar_hsa_circ_240739,RMVar_hsa_circ_339507,RMVar_hsa_circ_314609,RMVar_hsa_circ_240743,RMVar_hsa_circ_240742,RMVar_hsa_circ_62630,RMVar_hsa_circ_5963,RMVar_hsa_circ_73169,RMVar_hsa_circ_282930,RMVar_hsa_circ_240745,RMVar_hsa_circ_374614,RMVar_hsa_circ_240746 7430 RMVar_ID_7430 Human_SNP_ID_291093956 A-to-I Human chr6 - 107919197 107919197 107919197 AAGGTTGAAATCAACTTCTGGCCAGGCGCGGTAGCTCATGCCTGTAATCCCAGCACTTTGGGAGG AAGGTTGAAATCAACTTCTGGCCAGGCGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGG T C SEC63 Ensembl:ENSG00000025796 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs936772182 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_173,RMVar_hsa_circ_48741,RMVar_hsa_circ_320968,RMVar_hsa_circ_35889,RMVar_hsa_circ_286430,RMVar_hsa_circ_325358,RMVar_hsa_circ_336658,RMVar_hsa_circ_240722,RMVar_hsa_circ_313956,RMVar_hsa_circ_240723,RMVar_hsa_circ_240724,RMVar_hsa_circ_80125,RMVar_hsa_circ_240727,RMVar_hsa_circ_307172,RMVar_hsa_circ_345929,RMVar_hsa_circ_276293,RMVar_hsa_circ_240728,RMVar_hsa_circ_362460,RMVar_hsa_circ_240730,RMVar_hsa_circ_89451,RMVar_hsa_circ_285183,RMVar_hsa_circ_240731,RMVar_hsa_circ_362975,RMVar_hsa_circ_240734,RMVar_hsa_circ_38924,RMVar_hsa_circ_350170,RMVar_hsa_circ_240735,RMVar_hsa_circ_240736,RMVar_hsa_circ_10920,RMVar_hsa_circ_335360,RMVar_hsa_circ_240741,RMVar_hsa_circ_282163,RMVar_hsa_circ_240740,RMVar_hsa_circ_240739,RMVar_hsa_circ_339507,RMVar_hsa_circ_314609,RMVar_hsa_circ_240743,RMVar_hsa_circ_240742,RMVar_hsa_circ_62630,RMVar_hsa_circ_5963,RMVar_hsa_circ_73169,RMVar_hsa_circ_282930,RMVar_hsa_circ_240745,RMVar_hsa_circ_374614,RMVar_hsa_circ_240746 7431 RMVar_ID_7431 Human_SNP_ID_291121839 A-to-I Human chr6 - 108028326 108028326 108028326 CACCACGCCTGGCTAATTTTTTTTGTATTTTTAGTAGAGACGGGGTTTCACTGTGTTGGTCGGGA CACCACGCCTGGCTAATTTTTTTTGTATTTTTGGTAGAGACGGGGTTTCACTGTGTTGGTCGGGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1473865800 Functional Loss SNV dbSNP153 33..33 33 - - - 7432 RMVar_ID_7432 Human_SNP_ID_291125216 A-to-I Human chr6 - 108042167 108042167 108042167 TTAGCCTCCCAAAGTGCTGGGATTACAAGCATAAGCACCACACCTGGCTGAACATCAGATATTTT TTAGCCTCCCAAAGTGCTGGGATTACAAGCATGAGCACCACACCTGGCTGAACATCAGATATTTT T C OSTM1 Ensembl:ENSG00000081087 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1046652 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_799890 RMVar_hsa_circ_265883 7433 RMVar_ID_7433 Human_SNP_ID_291125232 A-to-I Human chr6 - 108042260 108042260 108042260 TTAATTTTTTTTTTTTTTTTTTTTGTAGAGACAGTGTCTCACTATGTTGCCCAAGCTGGTCTTGA TTAATTTTTTTTTTTTTTTTTTTTGTAGAGACGGTGTCTCACTATGTTGCCCAAGCTGGTCTTGA T C OSTM1 Ensembl:ENSG00000081087 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1476063569 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_799890 RMVar_hsa_circ_265883 7434 RMVar_ID_7434 Human_SNP_ID_291125328 A-to-I Human chr6 - 108042419 108042419 108042419 AGAGCCAGACCTTGTCTCAAAAAAAAAAAAAAAAAAAGAAAAAAGAAAGTACTGTCTGTCTTAAA AGAGCCAGACCTTGTCTCAAAAAAAAAAAAAAGAAAAGAAAAAAGAAAGTACTGTCTGTCTTAAA T C OSTM1 Ensembl:ENSG00000081087 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs564822548 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25949725 RMVar_hsa_circ_265883 7435 RMVar_ID_7435 Human_SNP_ID_291125406 A-to-I Human chr6 - 108042691 108042691 108042691 ATGAGTACCATCAGCTGGACACAGTGTCTCATACCTGTATTTGCAGCACTTTGGGAGGCTGAAGC ATGAGTACCATCAGCTGGACACAGTGTCTCATGCCTGTATTTGCAGCACTTTGGGAGGCTGAAGC T C OSTM1 Ensembl:ENSG00000081087 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs3198289 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22618985 RMVar_hsa_circ_265883 7436 RMVar_ID_7436 Human_SNP_ID_291131340 A-to-I Human chr6 - 108068084 108068084 108068084 ATTTGTGTCAAATCCTGCTGAGAGAATTGGAGATATATCTGTCAACACTGGCAGTATTGGTGACA ATTTGTGTCAAATCCTGCTGAGAGAATTGGAGGTATATCTGTCAACACTGGCAGTATTGGTGACA T C OSTM1 Ensembl:ENSG00000081087 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1231271283 Functional Loss SNV dbSNP153 33..33 33 - - - 7437 RMVar_ID_7437 Human_SNP_ID_291131361 A-to-I Human chr6 - 108068173 108068171 108068174 AAGGTGACTGAGAAGGAAGAATTGGAGAGATAAAGAAGAATGAGGAGAGCATGATGCCCTGTAAA AAGGTGACTGAGAAGGAAGAATTGGAGAGAT___GAAGAATGAGGAGAGCATGATGCCCTGTAAA CTTT C OSTM1 Ensembl:ENSG00000081087 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs534746955 Functional Loss DEL dbSNP153 32..34 33 - - - 7438 RMVar_ID_7438 Human_SNP_ID_291168437 A-to-I Human chr6 - 108221657 108221657 108221657 CCTGTAGTCCCAGCACTCAGGAGGCTGAGGCAAGAGGATCACTTTGAGTCCAGGAGGCAGAGGTT CCTGTAGTCCCAGCACTCAGGAGGCTGAGGCAGGAGGATCACTTTGAGTCCAGGAGGCAGAGGTT T C SNX3 Ensembl:ENSG00000112335 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1436305857 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86247,RMVar_hsa_circ_113806,RMVar_hsa_circ_240755,RMVar_hsa_circ_240756,RMVar_hsa_circ_301194 7439 RMVar_ID_7439 Human_SNP_ID_291175131 A-to-I Human chr6 - 108247446 108247445 108247446 GAAGGATCACTTGAGCCCAAGTGGTTGAGGCTACATTAAGCCGTGGTCGTGCCACTGCACTCCAG GAAGGATCACTTGAGCCCAAGTGGTTGAGGCT_CATTAAGCCGTGGTCGTGCCACTGCACTCCAG GT G SNX3 Ensembl:ENSG00000112335 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1286891819 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_86247,RMVar_hsa_circ_240755 7440 RMVar_ID_7440 Human_SNP_ID_291175132 A-to-I Human chr6 - 108247446 108247446 108247446 GAAGGATCACTTGAGCCCAAGTGGTTGAGGCTACATTAAGCCGTGGTCGTGCCACTGCACTCCAG GAAGGATCACTTGAGCCCAAGTGGTTGAGGCTTCATTAAGCCGTGGTCGTGCCACTGCACTCCAG T A SNX3 Ensembl:ENSG00000112335 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs539594846 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86247,RMVar_hsa_circ_240755 7441 RMVar_ID_7441 Human_SNP_ID_291175241 A-to-I Human chr6 - 108247876 108247876 108247876 CCAGGCTGGTTTTGAACTCCTGAGCTCAAGCAATCCTCCTGCCTCTGCCTCCCAAAGTGCTGGGA CCAGGCTGGTTTTGAACTCCTGAGCTCAAGCAGTCCTCCTGCCTCTGCCTCCCAAAGTGCTGGGA T C SNX3 Ensembl:ENSG00000112335 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs542377418 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86247,RMVar_hsa_circ_240755 7442 RMVar_ID_7442 Human_SNP_ID_291177300 A-to-I Human chr6 - 108256064 108256064 108256064 CACCACACCCAGCTAATTTTTAAATTATTTGTAGAGACGAGATCTCACTATGTTGCCCAGGCTGC CACCACACCCAGCTAATTTTTAAATTATTTGTGGAGACGAGATCTCACTATGTTGCCCAGGCTGC T C SNX3 Ensembl:ENSG00000112335 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs556653882 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86247,RMVar_hsa_circ_240755 7443 RMVar_ID_7443 Human_SNP_ID_291177617 A-to-I Human chr6 - 108257427 108257427 108257427 CTCACTGCATTCTCAAACTCGAGGACTCAAGTATTCCCCCCGCCTCAGCCTCCCAAGTAGCTGGA CTCACTGCATTCTCAAACTCGAGGACTCAAGTGTTCCCCCCGCCTCAGCCTCCCAAGTAGCTGGA T C SNX3 Ensembl:ENSG00000112335 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs908968991 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15591089 RMVar_hsa_circ_86247,RMVar_hsa_circ_240755 7444 RMVar_ID_7444 Human_SNP_ID_291187873 A-to-I Human chr6 + 108297368 108297368 108297368 GACCTCAGGTGATCCGGAGCCTCGGCCCCCCAAAATGCTGGGATTACAGGCGTGAGCCATGGTGC GACCTCAGGTGATCCGGAGCCTCGGCCCCCCAGAATGCTGGGATTACAGGCGTGAGCCATGGTGC A G AFG1L Ensembl:ENSG00000135537 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs113255499 Functional Loss SNV dbSNP153 33..33 33 - - - 7445 RMVar_ID_7445 Human_SNP_ID_291252054 A-to-I Human chr6 + 108585736 108585736 108585736 CAGAGGCTACTTAGGGTGCCTTAGGAAAAGGTATCGTTATTATTATTCCATTAGTCTGTAACCTT CAGAGGCTACTTAGGGTGCCTTAGGAAAAGGTTTCGTTATTATTATTCCATTAGTCTGTAACCTT A T FOXO3 Ensembl:ENSG00000118689 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs989855985 Functional Loss SNV dbSNP153 33..33 33 - - - 7446 RMVar_ID_7446 Human_SNP_ID_291252056 A-to-I Human chr6 + 108585742 108585739 108585742 CTACTTAGGGTGCCTTAGGAAAAGGTATCGTTATTATTATTCCATTAGTCTGTAACCTTCTAGAT CTACTTAGGGTGCCTTAGGAAAAGGTATCG___TTATTATTCCATTAGTCTGTAACCTTCTAGAT GTTA G FOXO3 Ensembl:ENSG00000118689 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1297077036 Functional Loss DEL dbSNP153 31..33 33 - - - 7447 RMVar_ID_7447 Human_SNP_ID_291252065 A-to-I Human chr6 + 108585778 108585778 108585778 TTATTCCATTAGTCTGTAACCTTCTAGATTTTAGCTGAATGAAACTCTAAACCACTTAAAACACA TTATTCCATTAGTCTGTAACCTTCTAGATTTTTGCTGAATGAAACTCTAAACCACTTAAAACACA A T FOXO3 Ensembl:ENSG00000118689 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs929493673 Functional Loss SNV dbSNP153 33..33 33 - - - 7448 RMVar_ID_7448 Human_SNP_ID_291297973 A-to-I Human chr6 - 108786163 108786163 108786163 CGTGCATCAGACCAATGAGGTGAAATCTGGAGAAGCAGTAGAACCCTTGGGCACCAGGATCACCC CGTGCATCAGACCAATGAGGTGAAATCTGGAGGAGCAGTAGAACCCTTGGGCACCAGGATCACCC T C ZNF259P1 Ensembl:ENSG00000219565 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs972845542 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18060053 7449 RMVar_ID_7449 Human_SNP_ID_291356185 A-to-I Human chr6 - 109041280 109041280 109041280 ATTTAGTTTTTGAGACAGAGTCTCACTCTGCCACCCAGACTGGCACAATCACAACTCACTGCAGC ATTTAGTTTTTGAGACAGAGTCTCACTCTGCCGCCCAGACTGGCACAATCACAACTCACTGCAGC T C SESN1 Ensembl:ENSG00000080546 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs931423378 Functional Loss SNV dbSNP153 33..33 33 - - - 7450 RMVar_ID_7450 Human_SNP_ID_291385456 A-to-I Human chr6 + 109167609 109167609 109167609 TGAGGCAGGATAATTGCTTGAACCTGGGAGGCAGAGGTTGCGGTGAGCCGAGATTGTGCCACTGC TGAGGCAGGATAATTGCTTGAACCTGGGAGGCGGAGGTTGCGGTGAGCCGAGATTGTGCCACTGC A G CCDC162P Ensembl:ENSG00000203799 Pseudogene intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1473009320 Functional Loss SNV dbSNP153 33..33 33 - - - 7451 RMVar_ID_7451 Human_SNP_ID_291385477 A-to-I Human chr6 + 109167664 109167664 109167664 GTGCCACTGCACTCCAGCCTGGGCAACAGAGCAAGACTCTGCCTCAAAGCAAAAAAAAAAAGAAA GTGCCACTGCACTCCAGCCTGGGCAACAGAGCTAGACTCTGCCTCAAAGCAAAAAAAAAAAGAAA A T CCDC162P Ensembl:ENSG00000203799 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1405695281 Functional Loss SNV dbSNP153 33..33 33 - - - 7452 RMVar_ID_7452 Human_SNP_ID_291385755 A-to-I Human chr6 + 109168779 109168779 109168779 CACCATGCCCTGCTAATTTTTTGTATTTTAGTAGAGATGGGGTTTCACTGTATTGCCCAGGCTGG CACCATGCCCTGCTAATTTTTTGTATTTTAGTTGAGATGGGGTTTCACTGTATTGCCCAGGCTGG A T CCDC162P Ensembl:ENSG00000203799 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1411737416 Functional Loss SNV dbSNP153 33..33 33 - - - 7453 RMVar_ID_7453 Human_SNP_ID_291385861 A-to-I Human chr6 + 109169127 109169127 109169127 ATGTGCCTGTAATCCCGGGTACTCGGGAGGCTAAGGCCAGAGGATTGCTTGAACCAGGGAGGCGG ATGTGCCTGTAATCCCGGGTACTCGGGAGGCTGAGGCCAGAGGATTGCTTGAACCAGGGAGGCGG A G CCDC162P Ensembl:ENSG00000203799 Pseudogene intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1392986226 Functional Loss SNV dbSNP153 33..33 33 - - - 7454 RMVar_ID_7454 Human_SNP_ID_291434514 A-to-I Human chr6 - 109375307 109375307 109375307 CAGCCTGTATTTTCTCTCTTAATGTAAGCATTATGGTATACACTTTACCCATCCTGCTCTTGATT CAGCCTGTATTTTCTCTCTTAATGTAAGCATTGTGGTATACACTTTACCCATCCTGCTCTTGATT T C CD164 Ensembl:ENSG00000135535 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1562239707 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90965,RMVar_hsa_circ_240814,RMVar_hsa_circ_355750,RMVar_hsa_circ_361793 7455 RMVar_ID_7455 Human_SNP_ID_291458344 A-to-I Human chr6 - 109464743 109464743 109464743 AGAGTGTAGTGGCACAATCATTGCTCACTGTAACCTCGAATTCCTGGGCTCAAGCAACCCTCCCA AGAGTGTAGTGGCACAATCATTGCTCACTGTAGCCTCGAATTCCTGGGCTCAAGCAACCCTCCCA T C MICAL1,ZBTB24 Ensembl:ENSG00000135596,Ensembl:ENSG00000112365 Protein coding,Protein coding intron,3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs11538252 Functional Loss SNV dbSNP153 33..33 33 - - - 7456 RMVar_ID_7456 Human_SNP_ID_291458353 A-to-I Human chr6 - 109464800 109464800 109464800 TATCTTCTCCTAATCTTTCCTTTTTTAGAGACAGGGTCTCACTGTATCACCCAGGCCAGAGTGTA TATCTTCTCCTAATCTTTCCTTTTTTAGAGACGGGGTCTCACTGTATCACCCAGGCCAGAGTGTA T C MICAL1,ZBTB24 Ensembl:ENSG00000135596,Ensembl:ENSG00000112365 Protein coding,Protein coding intron,3'UTR GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs1192479754 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7517454,Human_RBP_ID_15597794 7457 RMVar_ID_7457 Human_SNP_ID_291467076 A-to-I Human chr6 - 109499731 109499731 109499731 AGCCGTCTGTGATGGTACACATCTGTAATCCTAGCTACTTGGGAGGCTGAGGCACAAGAATCACT AGCCGTCTGTGATGGTACACATCTGTAATCCTGGCTACTTGGGAGGCTGAGGCACAAGAATCACT T C AK9 Ensembl:ENSG00000155085 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1246642653 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45731,RMVar_hsa_circ_353699 7458 RMVar_ID_7458 Human_SNP_ID_291467084 A-to-I Human chr6 - 109499763 109499763 109499763 AAACCCTGTCTCTACTAAAAGTACAAAAAATTAGCCGTCTGTGATGGTACACATCTGTAATCCTA AAACCCTGTCTCTACTAAAAGTACAAAAAATTTGCCGTCTGTGATGGTACACATCTGTAATCCTA T A AK9 Ensembl:ENSG00000155085 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs149744860 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45731,RMVar_hsa_circ_353699 7459 RMVar_ID_7459 Human_SNP_ID_291623848 A-to-I Human chr6 - 110153363 110153363 110153363 ACATTGTACAGCTAGTTATTTTTATCTGCCATAAGGTCAAACTGGAACAGAAACCAGAACAGTAG ACATTGTACAGCTAGTTATTTTTATCTGCCATGAGGTCAAACTGGAACAGAAACCAGAACAGTAG T C WASF1 Ensembl:ENSG00000112290 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs987094641 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63606,RMVar_hsa_circ_25384,RMVar_hsa_circ_240889,RMVar_hsa_circ_285803 7460 RMVar_ID_7460 Human_SNP_ID_291623850 A-to-I Human chr6 - 110153365 110153365 110153365 TTACATTGTACAGCTAGTTATTTTTATCTGCCATAAGGTCAAACTGGAACAGAAACCAGAACAGT TTACATTGTACAGCTAGTTATTTTTATCTGCCGTAAGGTCAAACTGGAACAGAAACCAGAACAGT T C WASF1 Ensembl:ENSG00000112290 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs534269856 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63606,RMVar_hsa_circ_25384,RMVar_hsa_circ_240889,RMVar_hsa_circ_285803 7461 RMVar_ID_7461 Human_SNP_ID_291641250 A-to-I Human chr6 + 110231234 110231234 110231234 TTATAAAATCAAGATAGTCCGGACGCGGTGGCACATGCCTGTAATCCCAGCACTTTGGGAGGCTG TTATAAAATCAAGATAGTCCGGACGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTG A T CDC40 Ensembl:ENSG00000168438 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1029476581 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7518297,Human_RBP_ID_8895221,Human_RBP_ID_15599826 Human_miRNA_ID_1333187 7462 RMVar_ID_7462 Human_SNP_ID_291731026 A-to-I Human chr6 - 110610454 110610454 110610454 AAAAAAACCCTTAATGCACTGTTATCTCCTAAATATTTAGTAAATTAATACTATTTAATTTTTTT AAAAAAACCCTTAATGCACTGTTATCTCCTAAGTATTTAGTAAATTAATACTATTTAATTTTTTT T C CDK19 Ensembl:ENSG00000155111 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs574292356 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_824737 RMVar_hsa_circ_100945,RMVar_hsa_circ_240902,RMVar_hsa_circ_84526,RMVar_hsa_circ_240901 7463 RMVar_ID_7463 Human_SNP_ID_291731027 A-to-I Human chr6 - 110610454 110610454 110610454 AAAAAAACCCTTAATGCACTGTTATCTCCTAAATATTTAGTAAATTAATACTATTTAATTTTTTT AAAAAAACCCTTAATGCACTGTTATCTCCTAACTATTTAGTAAATTAATACTATTTAATTTTTTT T G CDK19 Ensembl:ENSG00000155111 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs574292356 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_824737 RMVar_hsa_circ_100945,RMVar_hsa_circ_240902,RMVar_hsa_circ_84526,RMVar_hsa_circ_240901 7464 RMVar_ID_7464 Human_SNP_ID_291737922 A-to-I Human chr6 - 110640900 110640900 110640900 CAGGCTTGAGTGCAATGGCACGCTCACAGCTCACTCTAGCCTCGACCTCCTGGGCTCAAGCAGTC CAGGCTTGAGTGCAATGGCACGCTCACAGCTCCCTCTAGCCTCGACCTCCTGGGCTCAAGCAGTC T G CDK19 Ensembl:ENSG00000155111 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs983935588 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54241,RMVar_hsa_circ_5890,RMVar_hsa_circ_100945,RMVar_hsa_circ_68844,RMVar_hsa_circ_240902,RMVar_hsa_circ_50434,RMVar_hsa_circ_80269,RMVar_hsa_circ_88718,RMVar_hsa_circ_240904,RMVar_hsa_circ_240906,RMVar_hsa_circ_78429,RMVar_hsa_circ_240905,RMVar_hsa_circ_240909,RMVar_hsa_circ_281979,RMVar_hsa_circ_318766,RMVar_hsa_circ_335812,RMVar_hsa_circ_240911,RMVar_hsa_circ_55201,RMVar_hsa_circ_302653,RMVar_hsa_circ_240910,RMVar_hsa_circ_306404,RMVar_hsa_circ_371744,RMVar_hsa_circ_277983,RMVar_hsa_circ_240912 7465 RMVar_ID_7465 Human_SNP_ID_291757081 A-to-I Human chr6 - 110722861 110722858 110722861 TAGAAGATCAGGAATCCTTTTTTTTTTGAGATAGGGTCTCACTCTGTCACCCAGGCTGTAGTACA TAGAAGATCAGGAATCCTTTTTTTTTTGAGAT___GTCTCACTCTGTCACCCAGGCTGTAGTACA CCCT C CDK19 Ensembl:ENSG00000155111 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1400848961 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_15600780 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 7466 RMVar_ID_7466 Human_SNP_ID_291757083 A-to-I Human chr6 - 110722861 110722861 110722861 TAGAAGATCAGGAATCCTTTTTTTTTTGAGATAGGGTCTCACTCTGTCACCCAGGCTGTAGTACA TAGAAGATCAGGAATCCTTTTTTTTTTGAGATGGGGTCTCACTCTGTCACCCAGGCTGTAGTACA T C CDK19 Ensembl:ENSG00000155111 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215696512 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15600780 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 7467 RMVar_ID_7467 Human_SNP_ID_291759298 A-to-I Human chr6 - 110732285 110732285 110732285 CGCCGTGACAGCCAGGCTAGTCTCAAATTCCTAACCTAAAGTGATCCACCTGCCTCCATCTCCGA CGCCGTGACAGCCAGGCTAGTCTCAAATTCCTCACCTAAAGTGATCCACCTGCCTCCATCTCCGA T G CDK19 Ensembl:ENSG00000155111 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1055357877 Functional Loss SNV dbSNP153 33..33 33 - - - 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 7468 RMVar_ID_7468 Human_SNP_ID_291764761 A-to-I Human chr6 - 110755315 110755315 110755315 TCACAAGGGGCTAGGCATGGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGTGAGGCAAGCG TCACAAGGGGCTAGGCATGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGTGAGGCAAGCG T C CDK19 Ensembl:ENSG00000155111 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs540862385 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50434,RMVar_hsa_circ_78429,RMVar_hsa_circ_240905,RMVar_hsa_circ_18043,RMVar_hsa_circ_55201,RMVar_hsa_circ_280451,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 7469 RMVar_ID_7469 Human_SNP_ID_291764762 A-to-I Human chr6 - 110755315 110755315 110755315 TCACAAGGGGCTAGGCATGGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGTGAGGCAAGCG TCACAAGGGGCTAGGCATGGTGGCTCACGCCTCTAATCCCAGCACTTTGGGAGGTGAGGCAAGCG T G CDK19 Ensembl:ENSG00000155111 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs540862385 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50434,RMVar_hsa_circ_78429,RMVar_hsa_circ_240905,RMVar_hsa_circ_18043,RMVar_hsa_circ_55201,RMVar_hsa_circ_280451,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 7470 RMVar_ID_7470 Human_SNP_ID_291766243 A-to-I Human chr6 - 110761194 110761194 110761194 CCTGTGGTCCCTGCTACTCTGGAGGCTGAGGCAGGAGGATGACTTGAGCCAAGGCATTCGAGACC CCTGTGGTCCCTGCTACTCTGGAGGCTGAGGCGGGAGGATGACTTGAGCCAAGGCATTCGAGACC T C CDK19 Ensembl:ENSG00000155111 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968788254 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50434,RMVar_hsa_circ_78429,RMVar_hsa_circ_240905,RMVar_hsa_circ_18043,RMVar_hsa_circ_55201,RMVar_hsa_circ_280451,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 7471 RMVar_ID_7471 Human_SNP_ID_291772496 A-to-I Human chr6 - 110787298 110787298 110787298 ACAATCTCCACTCACTGCAAACTCTGCCTCCCAGGTTCAAACGATTCTCCTGCCTCAGCCTCCCA ACAATCTCCACTCACTGCAAACTCTGCCTCCCCGGTTCAAACGATTCTCCTGCCTCAGCCTCCCA T G CDK19 Ensembl:ENSG00000155111 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946608675 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_240919,RMVar_hsa_circ_240918 7472 RMVar_ID_7472 Human_SNP_ID_291791007 A-to-I Human chr6 + 110858764 110858764 110858764 CCATCGGGCTGCAGATGGGCACCAACAAATGCACCAGCCAGTCGGGCATGACCGCGTACAGCACA CCATCGGGCTGCAGATGGGCACCAACAAATGCCCCAGCCAGTCGGGCATGACCGCGTACAGCACA A C CNN2P9 Ensembl:ENSG00000213149 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900162570 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17422369 7473 RMVar_ID_7473 Human_SNP_ID_291791008 A-to-I Human chr6 + 110858764 110858764 110858764 CCATCGGGCTGCAGATGGGCACCAACAAATGCACCAGCCAGTCGGGCATGACCGCGTACAGCACA CCATCGGGCTGCAGATGGGCACCAACAAATGCTCCAGCCAGTCGGGCATGACCGCGTACAGCACA A T CNN2P9 Ensembl:ENSG00000213149 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900162570 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17422369 7474 RMVar_ID_7474 Human_SNP_ID_291797187 A-to-I Human chr6 + 110882216 110882216 110882216 TGCAGTGGCACGATCTTGGCTCACTGCAACCTAATTTTAAAAATGGCTCTGTCGACTGTATAAAG TGCAGTGGCACGATCTTGGCTCACTGCAACCTGATTTTAAAAATGGCTCTGTCGACTGTATAAAG A G AMD1 Ensembl:ENSG00000123505 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1279596 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_434,GWAS_ID_435,GWAS_ID_436,GWAS_ID_437,GWAS_ID_438,GWAS_ID_439,GWAS_ID_440,GWAS_ID_441,GWAS_ID_442,GWAS_ID_443,GWAS_ID_444,GWAS_ID_445,GWAS_ID_446,GWAS_ID_447,GWAS_ID_448,GWAS_ID_449,GWAS_ID_450,GWAS_ID_451 RMVar_hsa_circ_112997,RMVar_hsa_circ_240925,RMVar_hsa_circ_89724,RMVar_hsa_circ_240924 7475 RMVar_ID_7475 Human_SNP_ID_291797700 A-to-I Human chr6 + 110884148 110884148 110884148 TTGGGTGGCAAATAAGTGGGGCAGATGCAAATAACATAGCAAAGGAGTTCATAACAAACCTGACA TTGGGTGGCAAATAAGTGGGGCAGATGCAAATGACATAGCAAAGGAGTTCATAACAAACCTGACA A G AMD1 Ensembl:ENSG00000123505 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1016113277 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112997,RMVar_hsa_circ_240925,RMVar_hsa_circ_89724,RMVar_hsa_circ_240924 7476 RMVar_ID_7476 Human_SNP_ID_291798327 A-to-I Human chr6 + 110886445 110886443 110886445 CCTCAGCCTCAGCCTCCTGAGTAGCTGAGATTATAAGCACCTGCCACCACGCCCGGCTAATTTTT CCTCAGCCTCAGCCTCCTGAGTAGCTGAGAT__TAAGCACCTGCCACCACGCCCGGCTAATTTTT TTA T AMD1 Ensembl:ENSG00000123505 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1321760852 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_112997,RMVar_hsa_circ_240925,RMVar_hsa_circ_89724,RMVar_hsa_circ_240924 7477 RMVar_ID_7477 Human_SNP_ID_291801048 A-to-I Human chr6 + 110896739 110896739 110896739 ACGTTTTTGTTCTGTCACCCAGGCTGGAGTGCAATGGCGTGATCTCGGCTCACTGCAACCTCCAC ACGTTTTTGTTCTGTCACCCAGGCTGGAGTGCGATGGCGTGATCTCGGCTCACTGCAACCTCCAC A G AMD1 Ensembl:ENSG00000123505 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs765852120 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7519312 7478 RMVar_ID_7478 Human_SNP_ID_291801155 A-to-I Human chr6 + 110897164 110897154 110897165 CTCTACAATAAATAAAAGGAAATTGAGGCTGTAATGAGCTGTGATTGTACCACTGTACTCTAGCC CTCTACAATAAATAAAAGGAAAT___________TGAGCTGTGATTGTACCACTGTACTCTAGCC TTGAGGCTGTAA T AMD1 Ensembl:ENSG00000123505 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1377650385 Functional Loss DEL dbSNP153 24..34 33 - - - Human_RBP_ID_2004774,Human_RBP_ID_15603117,Human_RBP_ID_22513063 7479 RMVar_ID_7479 Human_SNP_ID_291801412 A-to-I Human chr6 + 110898071 110898071 110898071 GGGAGTGGTGGCGCATGCCTGTAGTCCCAGCTACTCAGAAGGCTGAGGCAGAAGAATCACTTGAA GGGAGTGGTGGCGCATGCCTGTAGTCCCAGCTGCTCAGAAGGCTGAGGCAGAAGAATCACTTGAA A G AMD1 Ensembl:ENSG00000123505 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs988552464 Functional Loss SNV dbSNP153 33..33 33 - - - 7480 RMVar_ID_7480 Human_SNP_ID_291801420 A-to-I Human chr6 + 110898102 110898102 110898102 TACTCAGAAGGCTGAGGCAGAAGAATCACTTGAACCCGGGAGGCTGAGGTTGCGGTGAGTCGAGA TACTCAGAAGGCTGAGGCAGAAGAATCACTTGGACCCGGGAGGCTGAGGTTGCGGTGAGTCGAGA A G AMD1 Ensembl:ENSG00000123505 Protein coding 3'UTR GSE38233;GSE107867 cultured B-cells;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 24183664,30559470 RNA-Seq:(High) rs564243033 Functional Loss SNV dbSNP153 33..33 33 - - - 7481 RMVar_ID_7481 Human_SNP_ID_291818190 A-to-I Human chr6 + 110962959 110962959 110962959 CACCACCAGGGCCAGCTAATTTTTGTATTTTTAGTATAGACGGGGTTTTACAGTGTTGGCCAGGA CACCACCAGGGCCAGCTAATTTTTGTATTTTTGGTATAGACGGGGTTTTACAGTGTTGGCCAGGA A G GTF3C6 Ensembl:ENSG00000155115 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1367150847 Functional Loss SNV dbSNP153 33..33 33 - - - 7482 RMVar_ID_7482 Human_SNP_ID_291819243 A-to-I Human chr6 + 110967136 110967135 110967137 GATCGTACCCACTGCACTCCAGCCTGGGTGACAGAGCGAGACTTTGTCTTAAAAAAAAAAACATT GATCGTACCCACTGCACTCCAGCCTGGGTGAC__AGCGAGACTTTGTCTTAAAAAAAAAAACATT CAG C GTF3C6 Ensembl:ENSG00000155115 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444136005 Functional Loss DEL dbSNP153 33..34 33 - - - 7483 RMVar_ID_7483 Human_SNP_ID_291819244 A-to-I Human chr6 + 110967136 110967136 110967136 GATCGTACCCACTGCACTCCAGCCTGGGTGACAGAGCGAGACTTTGTCTTAAAAAAAAAAACATT GATCGTACCCACTGCACTCCAGCCTGGGTGACGGAGCGAGACTTTGTCTTAAAAAAAAAAACATT A G GTF3C6 Ensembl:ENSG00000155115 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1338417321 Functional Loss SNV dbSNP153 33..33 33 - - - 7484 RMVar_ID_7484 Human_SNP_ID_291819511 A-to-I Human chr6 + 110968162 110968144 110968163 TTAGAATTAGCTGGACATAGTGTCGTGTGCCTATGGTACCAGCTACTGGGCAGCTGACGTGGGAG TTAGAATTAGCTGGA___________________GGTACCAGCTACTGGGCAGCTGACGTGGGAG ACATAGTGTCGTGTGCCTAT A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1199402843 Functional Loss DEL dbSNP153 16..34 33 - - - Human_RBP_ID_7519379 7485 RMVar_ID_7485 Human_SNP_ID_291819513 A-to-I Human chr6 + 110968162 110968149 110968163 TTAGAATTAGCTGGACATAGTGTCGTGTGCCTATGGTACCAGCTACTGGGCAGCTGACGTGGGAG TTAGAATTAGCTGGACATAG______________GGTACCAGCTACTGGGCAGCTGACGTGGGAG GTGTCGTGTGCCTAT G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1342209432 Functional Loss DEL dbSNP153 21..34 33 - - - Human_RBP_ID_7519379 7486 RMVar_ID_7486 Human_SNP_ID_291819520 A-to-I Human chr6 + 110968162 110968162 110968162 TTAGAATTAGCTGGACATAGTGTCGTGTGCCTATGGTACCAGCTACTGGGCAGCTGACGTGGGAG TTAGAATTAGCTGGACATAGTGTCGTGTGCCTGTGGTACCAGCTACTGGGCAGCTGACGTGGGAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs561452040 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7519379 7487 RMVar_ID_7487 Human_SNP_ID_291819827 A-to-I Human chr6 + 110969156 110969156 110969156 ATAATCTCCCTTTTTTTTTTTGAGACAGTCTCACGCTGTTGCCCAGGCTGGAGTGCAGTGGCAAG ATAATCTCCCTTTTTTTTTTTGAGACAGTCTCGCGCTGTTGCCCAGGCTGGAGTGCAGTGGCAAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1168508686 Functional Loss SNV dbSNP153 33..33 33 - - - 7488 RMVar_ID_7488 Human_SNP_ID_291819845 A-to-I Human chr6 + 110969199 110969199 110969199 CAGGCTGGAGTGCAGTGGCAAGATCTCTGCTCACTGCAAGCTCCGCCTCCCGAGTTCACGCCATT CAGGCTGGAGTGCAGTGGCAAGATCTCTGCTCGCTGCAAGCTCCGCCTCCCGAGTTCACGCCATT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1280587838 Functional Loss SNV dbSNP153 33..33 33 - - - 7489 RMVar_ID_7489 Human_SNP_ID_291819861 A-to-I Human chr6 + 110969264 110969264 110969264 CTCCTGCCTCAGCCTCCCGAGTGGCTGGGACTACAGGTGACCACCACCATGCCTGGCTAATTTTT CTCCTGCCTCAGCCTCCCGAGTGGCTGGGACTGCAGGTGACCACCACCATGCCTGGCTAATTTTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1236535086 Functional Loss SNV dbSNP153 33..33 33 - - - 7490 RMVar_ID_7490 Human_SNP_ID_291820083 A-to-I Human chr6 + 110969946 110969946 110969946 CCTGGCTGTGTTTTTTTTAATTTTTTTTGAAGAGATGGGGTCTCATTATGTTGCCCAGGCTGGTC CCTGGCTGTGTTTTTTTTAATTTTTTTTGAAGGGATGGGGTCTCATTATGTTGCCCAGGCTGGTC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs762447786 Functional Loss SNV dbSNP153 33..33 33 - - - 7491 RMVar_ID_7491 Human_SNP_ID_291820290 A-to-I Human chr6 + 110970856 110970856 110970856 TTTTTTTTTTTTTTAAATCAAGTTCTGGCTCTATCACCCAGGCTGTAGTGCAGTGGCACAATCTG TTTTTTTTTTTTTTAAATCAAGTTCTGGCTCTGTCACCCAGGCTGTAGTGCAGTGGCACAATCTG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1012909925 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15603383 7492 RMVar_ID_7492 Human_SNP_ID_291820867 A-to-I Human chr6 + 110973305 110973305 110973305 GACTTTGGGAGGCCAAAGCAGGAGGACTGCCTAAACTAGGAGTTCAAGACCAGCCTGGGCAAGAT GACTTTGGGAGGCCAAAGCAGGAGGACTGCCTGAACTAGGAGTTCAAGACCAGCCTGGGCAAGAT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1394414994 Functional Loss SNV dbSNP153 33..33 33 - - - 7493 RMVar_ID_7493 Human_SNP_ID_291824329 A-to-I Human chr6 + 110986692 110986692 110986692 AGGCATAGTATGGGCCAGGCACAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGT AGGCATAGTATGGGCCAGGCACAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGT A G RPF2 Ensembl:ENSG00000197498 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1164390467 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42743,RMVar_hsa_circ_322095,RMVar_hsa_circ_375247,RMVar_hsa_circ_69969,RMVar_hsa_circ_25677,RMVar_hsa_circ_240936 7494 RMVar_ID_7494 Human_SNP_ID_291825916 A-to-I Human chr6 + 110992808 110992808 110992808 CCTTAAGAAAATCATCAGGGGCCAGACACAGTAGCTCACGCCTGTAATCCCAGCACTTTGGGAGG CCTTAAGAAAATCATCAGGGGCCAGACACAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGG A G RPF2 Ensembl:ENSG00000197498 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893151873 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17830,RMVar_hsa_circ_322095,RMVar_hsa_circ_69969,RMVar_hsa_circ_25677,RMVar_hsa_circ_353526 7495 RMVar_ID_7495 Human_SNP_ID_291826008 A-to-I Human chr6 + 110993179 110993179 110993179 GTTGCCCAATCTGGTTTTAAACTCCTGAGCTCAAATGATCTGCCTGCCTTGGCCTCCTAAAGTAC GTTGCCCAATCTGGTTTTAAACTCCTGAGCTCGAATGATCTGCCTGCCTTGGCCTCCTAAAGTAC A G RPF2 Ensembl:ENSG00000197498 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs763684668 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8627575 RMVar_hsa_circ_17830,RMVar_hsa_circ_322095,RMVar_hsa_circ_69969,RMVar_hsa_circ_25677,RMVar_hsa_circ_353526 7496 RMVar_ID_7496 Human_SNP_ID_291826769 A-to-I Human chr6 + 110996001 110996001 110996001 ACCATACCCAGCTAATTTTTTGTATTTTTCTTAGAGACAGGGTTTCACTATGTTGCTCAGGCTGG ACCATACCCAGCTAATTTTTTGTATTTTTCTTCGAGACAGGGTTTCACTATGTTGCTCAGGCTGG A C RPF2 Ensembl:ENSG00000197498 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1484062152 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15603787 RMVar_hsa_circ_17830,RMVar_hsa_circ_322095,RMVar_hsa_circ_69969,RMVar_hsa_circ_25677,RMVar_hsa_circ_353526 7497 RMVar_ID_7497 Human_SNP_ID_291827497 A-to-I Human chr6 + 110998834 110998834 110998834 AAGAAATAGATTACACACCTGTAATCCTAGTTACACAGGAGGCTAAGACAGGAGAATTGTTTGAA AAGAAATAGATTACACACCTGTAATCCTAGTTGCACAGGAGGCTAAGACAGGAGAATTGTTTGAA A G RPF2 Ensembl:ENSG00000197498 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1244347233 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17830,RMVar_hsa_circ_322095,RMVar_hsa_circ_25677,RMVar_hsa_circ_13088,RMVar_hsa_circ_278146,RMVar_hsa_circ_353526 7498 RMVar_ID_7498 Human_SNP_ID_291827499 A-to-I Human chr6 + 110998838 110998838 110998838 AATAGATTACACACCTGTAATCCTAGTTACACAGGAGGCTAAGACAGGAGAATTGTTTGAACCAG AATAGATTACACACCTGTAATCCTAGTTACACGGGAGGCTAAGACAGGAGAATTGTTTGAACCAG A G RPF2 Ensembl:ENSG00000197498 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1436613334 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17830,RMVar_hsa_circ_322095,RMVar_hsa_circ_25677,RMVar_hsa_circ_13088,RMVar_hsa_circ_278146,RMVar_hsa_circ_353526 7499 RMVar_ID_7499 Human_SNP_ID_291829342 A-to-I Human chr6 + 111006290 111006290 111006290 ATGGCATCTCGCTCTCACCCAAGCTAGAGTGCAGTGGTGCAATCTCGGCTCACTACAACCTCTGT ATGGCATCTCGCTCTCACCCAAGCTAGAGTGCGGTGGTGCAATCTCGGCTCACTACAACCTCTGT A G RPF2 Ensembl:ENSG00000197498 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs560029053 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17830,RMVar_hsa_circ_322095,RMVar_hsa_circ_37969,RMVar_hsa_circ_13088,RMVar_hsa_circ_278146,RMVar_hsa_circ_353526 7500 RMVar_ID_7500 Human_SNP_ID_291889794 A-to-I Human chr6 + 111267566 111267566 111267566 GAAATGGGCCGGGTGCAGTGGCTAAAGCCTGTAATCCCAGCACTTTGGGAGGCCGAGACGGGCAG GAAATGGGCCGGGTGCAGTGGCTAAAGCCTGTGATCCCAGCACTTTGGGAGGCCGAGACGGGCAG A G MFSD4B Ensembl:ENSG00000173214 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs763473823 Functional Loss SNV dbSNP153 33..33 33 - - - 7501 RMVar_ID_7501 Human_SNP_ID_291890232 A-to-I Human chr6 + 111269255 111269255 111269255 GGTGTCTCACTCTGTCACTCAGGCTGGAGTGCAATGACGTGATCTCAGCTCACTGCAACCTCTGC GGTGTCTCACTCTGTCACTCAGGCTGGAGTGCTATGACGTGATCTCAGCTCACTGCAACCTCTGC A T MFSD4B Ensembl:ENSG00000173214 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1299656910 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25952817 7502 RMVar_ID_7502 Human_SNP_ID_291890255 A-to-I Human chr6 + 111269339 111269339 111269339 CTTCTGCCTCGGCCTCCTGAGTAGCTGGGATTACAGGCATGCGCCACCATGCCCAGCTAATTTTT CTTCTGCCTCGGCCTCCTGAGTAGCTGGGATTGCAGGCATGCGCCACCATGCCCAGCTAATTTTT A G MFSD4B Ensembl:ENSG00000173214 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs528561990 Functional Loss SNV dbSNP153 33..33 33 - - - 7503 RMVar_ID_7503 Human_SNP_ID_291890511 A-to-I Human chr6 + 111270412 111270412 111270412 AGTTCTAAAAACTGAGCTAAGAGCAGGACATGATGGCTCACACCTGTAATCCCAGCTACTCAGGA AGTTCTAAAAACTGAGCTAAGAGCAGGACATGTTGGCTCACACCTGTAATCCCAGCTACTCAGGA A T MFSD4B Ensembl:ENSG00000173214 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs534324430 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15605474 7504 RMVar_ID_7504 Human_SNP_ID_291890760 A-to-I Human chr6 + 111271131 111271131 111271131 GGTGCGGTGGCTCACGCCAAGATGGCGCCACTACACTCCAGCCTGGGCAACAGAGGGAGACTCCA GGTGCGGTGGCTCACGCCAAGATGGCGCCACTGCACTCCAGCCTGGGCAACAGAGGGAGACTCCA A G MFSD4B Ensembl:ENSG00000173214 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1478906615 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26041784 7505 RMVar_ID_7505 Human_SNP_ID_291890900 A-to-I Human chr6 + 111271676 111271676 111271676 TCCAGAACTTTTGGCTGGGCATGGTGGCTCACACCTGTAATCACAGCACTTTGGGAGGCTGAGGT TCCAGAACTTTTGGCTGGGCATGGTGGCTCACCCCTGTAATCACAGCACTTTGGGAGGCTGAGGT A C MFSD4B Ensembl:ENSG00000173214 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1239533303 Functional Loss SNV dbSNP153 33..33 33 - - - 7506 RMVar_ID_7506 Human_SNP_ID_291891016 A-to-I Human chr6 + 111271883 111271883 111271883 CCCACTTCTGGGGAGGCTGAGGCACGAGAATCACTTGAACTTGGGAGGCAGAGTTTACAGTAAGC CCCACTTCTGGGGAGGCTGAGGCACGAGAATCGCTTGAACTTGGGAGGCAGAGTTTACAGTAAGC A G MFSD4B Ensembl:ENSG00000173214 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1243469471 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15605509 7507 RMVar_ID_7507 Human_SNP_ID_291891208 A-to-I Human chr6 + 111272611 111272611 111272611 TCTGCTCACTGCAACCTCTGTCTCCCAGGTTCAAGCCATTCTCATTCCTCAGCCACCCAAGTAGC TCTGCTCACTGCAACCTCTGTCTCCCAGGTTCCAGCCATTCTCATTCCTCAGCCACCCAAGTAGC A C MFSD4B Ensembl:ENSG00000173214 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs572321308 Functional Loss SNV dbSNP153 33..33 33 - - - 7508 RMVar_ID_7508 Human_SNP_ID_291891212 A-to-I Human chr6 + 111272622 111272622 111272622 CAACCTCTGTCTCCCAGGTTCAAGCCATTCTCATTCCTCAGCCACCCAAGTAGCTGGGATTACAG CAACCTCTGTCTCCCAGGTTCAAGCCATTCTCCTTCCTCAGCCACCCAAGTAGCTGGGATTACAG A C MFSD4B Ensembl:ENSG00000173214 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs924833965 Functional Loss SNV dbSNP153 33..33 33 - - - 7509 RMVar_ID_7509 Human_SNP_ID_291891213 A-to-I Human chr6 + 111272622 111272622 111272622 CAACCTCTGTCTCCCAGGTTCAAGCCATTCTCATTCCTCAGCCACCCAAGTAGCTGGGATTACAG CAACCTCTGTCTCCCAGGTTCAAGCCATTCTCGTTCCTCAGCCACCCAAGTAGCTGGGATTACAG A G MFSD4B Ensembl:ENSG00000173214 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs924833965 Functional Loss SNV dbSNP153 33..33 33 - - - 7510 RMVar_ID_7510 Human_SNP_ID_291891404 A-to-I Human chr6 + 111273254 111273254 111273254 CTCACTGCAGTCTCAAGCTTTTAGGCTCAAGCAGTCCCCTGCCTCAGCCTTCTGAGCAACTAGGA CTCACTGCAGTCTCAAGCTTTTAGGCTCAAGCGGTCCCCTGCCTCAGCCTTCTGAGCAACTAGGA A G MFSD4B Ensembl:ENSG00000173214 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042873345 Functional Loss SNV dbSNP153 33..33 33 - - - 7511 RMVar_ID_7511 Human_SNP_ID_291891405 A-to-I Human chr6 + 111273254 111273254 111273254 CTCACTGCAGTCTCAAGCTTTTAGGCTCAAGCAGTCCCCTGCCTCAGCCTTCTGAGCAACTAGGA CTCACTGCAGTCTCAAGCTTTTAGGCTCAAGCTGTCCCCTGCCTCAGCCTTCTGAGCAACTAGGA A T MFSD4B Ensembl:ENSG00000173214 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042873345 Functional Loss SNV dbSNP153 33..33 33 - - - 7512 RMVar_ID_7512 Human_SNP_ID_291891575 A-to-I Human chr6 + 111273825 111273825 111273825 ACGGCTCACTGTAGTTTTGACCTCCTGAGCTCAAGTGATTCTCTTGCTTCAGCCTTTTGAGTAGT ACGGCTCACTGTAGTTTTGACCTCCTGAGCTCCAGTGATTCTCTTGCTTCAGCCTTTTGAGTAGT A C MFSD4B Ensembl:ENSG00000173214 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1212166740 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15605583 7513 RMVar_ID_7513 Human_SNP_ID_291891641 A-to-I Human chr6 + 111274056 111274056 111274056 TTTTAAATTATTTCTAGAGACAAGGTCTCACTATGTTGCGCAGGCTGGTCTCAAACTCCTGGGCT TTTTAAATTATTTCTAGAGACAAGGTCTCACTGTGTTGCGCAGGCTGGTCTCAAACTCCTGGGCT A G MFSD4B Ensembl:ENSG00000173214 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1176677244 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27086656 7514 RMVar_ID_7514 Human_SNP_ID_291892674 A-to-I Human chr6 + 111278449 111278449 111278449 CAACGTCTTTCTTTTCTGATGGTGATTGATATAGTTTGGCTGTGTCCCCACCCAAATCTCATCTT CAACGTCTTTCTTTTCTGATGGTGATTGATATTGTTTGGCTGTGTCCCCACCCAAATCTCATCTT A T MFSD4B Ensembl:ENSG00000173214 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs951333708 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15605806,Human_RBP_ID_18851697 Human_Splice_Rec_802392,Human_Splice_Rec_802408,Human_Splice_Rec_802442,Human_Splice_Rec_802446,Human_Splice_Rec_802458,Human_Splice_Rec_802462 Human_miRNA_ID_3192550 7515 RMVar_ID_7515 Human_SNP_ID_291895782 A-to-I Human chr6 + 111290979 111290979 111290979 AGCACCCCACTCTAGTACCAACTCACTGTATTAGTCTGTTTTCACACTGCTGATAAAGACATACC AGCACCCCACTCTAGTACCAACTCACTGTATTGGTCTGTTTTCACACTGCTGATAAAGACATACC A G MFSD4B Ensembl:ENSG00000173214 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1441001716 Functional Loss SNV dbSNP153 33..33 33 - - - 7516 RMVar_ID_7516 Human_SNP_ID_291895793 A-to-I Human chr6 + 111291046 111291045 111291046 AGACTGGGTAATTTGTAAAGAAAAAGAGGTTTAATGGACTCAGTTCCACGTGGCTGGGGAGGCCT AGACTGGGTAATTTGTAAAGAAAAAGAGGTTT_ATGGACTCAGTTCCACGTGGCTGGGGAGGCCT TA T MFSD4B Ensembl:ENSG00000173214 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1156938198 Functional Loss DEL dbSNP153 33..33 33 - - - 7517 RMVar_ID_7517 Human_SNP_ID_291896214 A-to-I Human chr6 + 111292757 111292756 111292757 ACATGGCGAAACCCCGTCTCTACTAAAAATACAAAAAAATTAGCTGGGCGTGGTGGCAGGCATTT ACATGGCGAAACCCCGTCTCTACTAAAAATAC_AAAAAATTAGCTGGGCGTGGTGGCAGGCATTT CA C MFSD4B Ensembl:ENSG00000173214 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs59174968 Functional Loss DEL dbSNP153 33..33 33 - - - 7518 RMVar_ID_7518 Human_SNP_ID_291896216 A-to-I Human chr6 + 111292757 111292757 111292757 ACATGGCGAAACCCCGTCTCTACTAAAAATACAAAAAAATTAGCTGGGCGTGGTGGCAGGCATTT ACATGGCGAAACCCCGTCTCTACTAAAAATACTAAAAAATTAGCTGGGCGTGGTGGCAGGCATTT A T MFSD4B Ensembl:ENSG00000173214 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1247589726 Functional Loss SNV dbSNP153 33..33 33 - - - 7519 RMVar_ID_7519 Human_SNP_ID_291896847 A-to-I Human chr6 + 111294990 111294990 111294990 GCTGGAGTGCAATGGCGCGATTTCTGCTCACTACAACCTCTGTCTCCTGGGTTCAAACGATTCTC GCTGGAGTGCAATGGCGCGATTTCTGCTCACTGCAACCTCTGTCTCCTGGGTTCAAACGATTCTC A G MFSD4B Ensembl:ENSG00000173214 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1245048417 Functional Loss SNV dbSNP153 33..33 33 - - - 7520 RMVar_ID_7520 Human_SNP_ID_291896945 A-to-I Human chr6 + 111295233 111295233 111295233 GCGATTCTCCTGCCTCAGCCTCCTGAGTAGCTAGGATTACAGGCACCCCCCACCACGTCTGGCTA GCGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCACCCCCCACCACGTCTGGCTA A G MFSD4B Ensembl:ENSG00000173214 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1422486152 Functional Loss SNV dbSNP153 33..33 33 - - - 7521 RMVar_ID_7521 Human_SNP_ID_291900201 A-to-I Human chr6 - 111305348 111305348 111305348 GGACTCAAGCAATCCTCCCACTTCAGCTGCCTAAGGGCTGGGATTACAGGCATGAACCATGATGC GGACTCAAGCAATCCTCCCACTTCAGCTGCCTCAGGGCTGGGATTACAGGCATGAACCATGATGC T G REV3L Ensembl:ENSG00000009413 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1416713460 Functional Loss SNV dbSNP153 33..33 33 - - - 7522 RMVar_ID_7522 Human_SNP_ID_291902608 A-to-I Human chr6 + 111314963 111314963 111314963 ACCTTGAATACCTGGGCTCAAGTGGTCCTCCTACTTCAGCCTCTGGAACAGCTGGGACTACAGGC ACCTTGAATACCTGGGCTCAAGTGGTCCTCCTGCTTCAGCCTCTGGAACAGCTGGGACTACAGGC A G MFSD4B Ensembl:ENSG00000173214 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs556080844 Functional Loss SNV dbSNP153 33..33 33 - - - 7523 RMVar_ID_7523 Human_SNP_ID_291939121 A-to-I Human chr6 - 111465186 111465186 111465186 ATCCTGGCTACTCAGGGGGCTGAGCCAGGAGAATCACTTGAACCCGGGAGGCAGAGGTTGCAGTG ATCCTGGCTACTCAGGGGGCTGAGCCAGGAGAGTCACTTGAACCCGGGAGGCAGAGGTTGCAGTG T C REV3L Ensembl:ENSG00000009413 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1290441903 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57503,RMVar_hsa_circ_77645,RMVar_hsa_circ_240969,RMVar_hsa_circ_8297,RMVar_hsa_circ_73262,RMVar_hsa_circ_93025,RMVar_hsa_circ_295421,RMVar_hsa_circ_240981,RMVar_hsa_circ_240989,RMVar_hsa_circ_240990,RMVar_hsa_circ_240991,RMVar_hsa_circ_329514,RMVar_hsa_circ_240996,RMVar_hsa_circ_240993,RMVar_hsa_circ_295409,RMVar_hsa_circ_241001,RMVar_hsa_circ_278158,RMVar_hsa_circ_241002,RMVar_hsa_circ_241004,RMVar_hsa_circ_319786,RMVar_hsa_circ_335691,RMVar_hsa_circ_241005 7524 RMVar_ID_7524 Human_SNP_ID_291945531 A-to-I Human chr6 + 111488062 111488062 111488062 CAGTCATAGATGTTACATGCTTGTTTTGTATTAACTTTGTTACTCTCTTGAGTTCCTGCACCTCA CAGTCATAGATGTTACATGCTTGTTTTGTATTTACTTTGTTACTCTCTTGAGTTCCTGCACCTCA A T TRAF3IP2-AS1 Ensembl:ENSG00000231889 lincRNA intron GSE100210;GSE107867 HepG2 cell line;ASD brains,temporal_cortex - 29129909,30559470 RNA-Seq:(High) rs535999999 Functional Loss SNV dbSNP153 33..33 33 - - - 7525 RMVar_ID_7525 Human_SNP_ID_291945536 A-to-I Human chr6 + 111488071 111488071 111488071 ATGTTACATGCTTGTTTTGTATTAACTTTGTTACTCTCTTGAGTTCCTGCACCTCATAGGTCCAC ATGTTACATGCTTGTTTTGTATTAACTTTGTTGCTCTCTTGAGTTCCTGCACCTCATAGGTCCAC A G TRAF3IP2-AS1 Ensembl:ENSG00000231889 lincRNA intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1194555593 Functional Loss SNV dbSNP153 33..33 33 - - - 7526 RMVar_ID_7526 Human_SNP_ID_291945862 A-to-I Human chr6 + 111489520 111489520 111489520 ATTGCTTGAGCCCAGGAGTTTAAGACCAGCCTAGGCAACATGGTGAAACCCTGTGGGACTGAGAG ATTGCTTGAGCCCAGGAGTTTAAGACCAGCCTGGGCAACATGGTGAAACCCTGTGGGACTGAGAG A G TRAF3IP2-AS1 Ensembl:ENSG00000231889 lincRNA intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1360171435 Functional Loss SNV dbSNP153 33..33 33 - - - 7527 RMVar_ID_7527 Human_SNP_ID_291951487 A-to-I Human chr6 + 111514710 111514709 111514711 GCTCAAATTTTTGTTTTGTTTTGTTTTGAGACAGAGTCTCACTTTGTCGCCCAGGCTGGAGTGCA GCTCAAATTTTTGTTTTGTTTTGTTTTGAGAC__AGTCTCACTTTGTCGCCCAGGCTGGAGTGCA CAG C TRAF3IP2-AS1 Ensembl:ENSG00000231889 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1357502323 Functional Loss DEL dbSNP153 33..34 33 - - - 7528 RMVar_ID_7528 Human_SNP_ID_291952504 A-to-I Human chr6 + 111519125 111519125 111519125 GGCTCACTGCAACCTCCACCTCCCAGGTTCAGACGATTCTCCTGTCTCAGCCCCCCAGGTGGCTG GGCTCACTGCAACCTCCACCTCCCAGGTTCAGCCGATTCTCCTGTCTCAGCCCCCCAGGTGGCTG A C TRAF3IP2-AS1 Ensembl:ENSG00000231889 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1194203370 Functional Loss SNV dbSNP153 33..33 33 - - - 7529 RMVar_ID_7529 Human_SNP_ID_291952536 A-to-I Human chr6 + 111519288 111519288 111519288 TCAAGTGATCTGCCTTCCAAACTGCTGGGATTACAGGCATGAGCCACCACACCGGACTCAATTCT TCAAGTGATCTGCCTTCCAAACTGCTGGGATTGCAGGCATGAGCCACCACACCGGACTCAATTCT A G TRAF3IP2-AS1 Ensembl:ENSG00000231889 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1002798355 Functional Loss SNV dbSNP153 33..33 33 - - - 7530 RMVar_ID_7530 Human_SNP_ID_291961128 A-to-I Human chr6 - 111558468 111558465 111558469 AGATCATGTCACTGCACTCTAGCTTGGGAGACAGAGCGAGACTCCGTCTCAAAAAACAAACAAAC AGATCATGTCACTGCACTCTAGCTTGGGAGA____GCGAGACTCCGTCTCAAAAAACAAACAAAC CTCTG C TRAF3IP2 Ensembl:ENSG00000056972 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1368336506 Functional Loss DEL dbSNP153 32..35 33 - - - 7531 RMVar_ID_7531 Human_SNP_ID_291965607 A-to-I Human chr6 + 111578608 111578608 111578608 AAGGTTTCAGTGAGTCGAGATCTCGCCACTGCACTCCACCCTAAGTGACAGAGTCAGATCCTGTC AAGGTTTCAGTGAGTCGAGATCTCGCCACTGCCCTCCACCCTAAGTGACAGAGTCAGATCCTGTC A C TRAF3IP2-AS1 Ensembl:ENSG00000231889 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1034168120 Functional Loss SNV dbSNP153 33..33 33 - - - 7532 RMVar_ID_7532 Human_SNP_ID_291965861 A-to-I Human chr6 + 111579652 111579651 111579652 TACTTAGGAGGCTGAGGTGGGAGGATCGCTTGAACCTGTAAGGTAGAGGTTGCAGTGAGTCAAGT TACTTAGGAGGCTGAGGTGGGAGGATCGCTTG_ACCTGTAAGGTAGAGGTTGCAGTGAGTCAAGT GA G TRAF3IP2-AS1 Ensembl:ENSG00000231889 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1361170905 Functional Loss DEL dbSNP153 33..33 33 - - - 7533 RMVar_ID_7533 Human_SNP_ID_291993731 A-to-I Human chr6 - 111698239 111698239 111698239 ATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCTGGGAGGTGGAGGTTGCGGTG ATCCCAGCTACTCAGGAGGCTGAGGCAGGAGACTCACTTGAACCTGGGAGGTGGAGGTTGCGGTG T G FYN Ensembl:ENSG00000010810 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs372075115 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_241017,RMVar_hsa_circ_241014,RMVar_hsa_circ_338829,RMVar_hsa_circ_324158,RMVar_hsa_circ_285441,RMVar_hsa_circ_300067,RMVar_hsa_circ_283713,RMVar_hsa_circ_241015,RMVar_hsa_circ_241016,RMVar_hsa_circ_241018,RMVar_hsa_circ_109879,RMVar_hsa_circ_241019,RMVar_hsa_circ_326460 7534 RMVar_ID_7534 Human_SNP_ID_291993733 A-to-I Human chr6 - 111698245 111698245 111698245 CCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCTGGGAGGTGGAGGTT CCTGTAATCCCAGCTACTCAGGAGGCTGAGGCGGGAGAATCACTTGAACCTGGGAGGTGGAGGTT T C FYN Ensembl:ENSG00000010810 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1388077918 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_241017,RMVar_hsa_circ_241014,RMVar_hsa_circ_338829,RMVar_hsa_circ_324158,RMVar_hsa_circ_285441,RMVar_hsa_circ_300067,RMVar_hsa_circ_283713,RMVar_hsa_circ_241015,RMVar_hsa_circ_241016,RMVar_hsa_circ_241018,RMVar_hsa_circ_109879,RMVar_hsa_circ_241019,RMVar_hsa_circ_326460 7535 RMVar_ID_7535 Human_SNP_ID_291993754 A-to-I Human chr6 - 111698311 111698311 111698311 CTGACCAGCATGGAGAAACCCTGCCTCTACTAAAAATACAAAATTAGCCGGGCATGGTGGTGCAT CTGACCAGCATGGAGAAACCCTGCCTCTACTACAAATACAAAATTAGCCGGGCATGGTGGTGCAT T G FYN Ensembl:ENSG00000010810 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1044463119 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_241017,RMVar_hsa_circ_241014,RMVar_hsa_circ_338829,RMVar_hsa_circ_324158,RMVar_hsa_circ_285441,RMVar_hsa_circ_300067,RMVar_hsa_circ_283713,RMVar_hsa_circ_241015,RMVar_hsa_circ_241016,RMVar_hsa_circ_241018,RMVar_hsa_circ_109879,RMVar_hsa_circ_241019,RMVar_hsa_circ_326460 7536 RMVar_ID_7536 Human_SNP_ID_293087896 A-to-I Human chr6 + 116164895 116164894 116164895 CATAAGGTCAGGAGATCGAGACCATCCTGGCTAACATGGTGAAACCCCGTCTCTACTAAAAAAAT CATAAGGTCAGGAGATCGAGACCATCCTGGCT_ACATGGTGAAACCCCGTCTCTACTAAAAAAAT TA T NT5DC1 Ensembl:ENSG00000178425 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs771597037 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_106830,RMVar_hsa_circ_114000,RMVar_hsa_circ_241086,RMVar_hsa_circ_108337,RMVar_hsa_circ_241087,RMVar_hsa_circ_241088 7537 RMVar_ID_7537 Human_SNP_ID_293088542 A-to-I Human chr6 + 116167451 116167451 116167451 AGCCAGGATGGTCTCAATCTCCTGGCCTTGTGATCCACTTGCCTTGGCCTCCCAAAGTGCTAGGA AGCCAGGATGGTCTCAATCTCCTGGCCTTGTGGTCCACTTGCCTTGGCCTCCCAAAGTGCTAGGA A G NT5DC1 Ensembl:ENSG00000178425 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1180319917 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106830,RMVar_hsa_circ_114000,RMVar_hsa_circ_241086,RMVar_hsa_circ_108337,RMVar_hsa_circ_241087,RMVar_hsa_circ_241088 7538 RMVar_ID_7538 Human_SNP_ID_293112756 A-to-I Human chr6 - 116273865 116273864 116273866 AGATTGAGCCATGGCACTCCAGCCTGGGGACAAGAGAGACTTCGTCTCAAAAAAAAAAAAAAACA AGATTGAGCCATGGCACTCCAGCCTGGGGAC__GAGAGACTTCGTCTCAAAAAAAAAAAAAAACA CTT C TSPYL1 Ensembl:ENSG00000189241 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1162522261 Functional Loss DEL dbSNP153 32..33 33 - - - 7539 RMVar_ID_7539 Human_SNP_ID_293117782 A-to-I Human chr6 + 116294299 116294299 116294299 TTTGGTTCAGCCTCCCAAAGTGTTGGGATTATAGGAGTGAGCCACTGTGCCTGGCCAAAAATGAT TTTGGTTCAGCCTCCCAAAGTGTTGGGATTATGGGAGTGAGCCACTGTGCCTGGCCAAAAATGAT A G DSE Ensembl:ENSG00000111817 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985501241 Functional Loss SNV dbSNP153 33..33 33 - - - 7540 RMVar_ID_7540 Human_SNP_ID_293121753 A-to-I Human chr6 + 116311880 116311880 116311880 AGTTATCACCATCCAAAATTACATTTACTTATATGTAAATGTAAAGCAGGGACTTGACAGTCTTA AGTTATCACCATCCAAAATTACATTTACTTATGTGTAAATGTAAAGCAGGGACTTGACAGTCTTA A G DSE Ensembl:ENSG00000111817 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1347852355 Functional Loss SNV dbSNP153 33..33 33 - - - 7541 RMVar_ID_7541 Human_SNP_ID_293200024 A-to-I Human chr6 - 116645873 116645873 116645873 GAGAAAAAAAACCGAACATTATGCTTACTAATACTTGATCCTGGATGTCCTTCTCGAGAAATGCA GAGAAAAAAAACCGAACATTATGCTTACTAATGCTTGATCCTGGATGTCCTTCTCGAGAAATGCA T C ZUP1 Ensembl:ENSG00000153975 Protein coding exon GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs764621157 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_651780,Human_RBP_ID_2005795,Human_RBP_ID_8895980,Human_RBP_ID_15617901,Human_RBP_ID_17304441,Human_RBP_ID_24130615,Human_RBP_ID_25955692,Human_RBP_ID_27748288 Human_Splice_Rec_804944 Human_miRNA_ID_2009767,Human_miRNA_ID_2281505,Human_miRNA_ID_2283069,Human_miRNA_ID_2631119 RMVar_hsa_circ_241103,RMVar_hsa_circ_113305,RMVar_hsa_circ_299784,RMVar_hsa_circ_325730,RMVar_hsa_circ_241100,RMVar_hsa_circ_313488,RMVar_hsa_circ_282023,RMVar_hsa_circ_241101,RMVar_hsa_circ_241102 7542 RMVar_ID_7542 Human_SNP_ID_293200271 A-to-I Human chr6 - 116646783 116646783 116646783 TTGCTTGAGCCCAGCAGTTTGAGACCAGCCTGAGTGACATAGTGAGACCCTGTCTCTACAAAAAC TTGCTTGAGCCCAGCAGTTTGAGACCAGCCTGGGTGACATAGTGAGACCCTGTCTCTACAAAAAC T C ZUP1 Ensembl:ENSG00000153975 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs992481812 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_241103,RMVar_hsa_circ_299784,RMVar_hsa_circ_325730,RMVar_hsa_circ_313488,RMVar_hsa_circ_282023,RMVar_hsa_circ_241101,RMVar_hsa_circ_241102 7543 RMVar_ID_7543 Human_SNP_ID_293200387 A-to-I Human chr6 - 116647350 116647349 116647351 TTTTTGTTTGTTTGTTTGTTTTTTTAGACAGAATCTCACTCTGTTGCTCAGGCTGGAGTGCAGTG TTTTTGTTTGTTTGTTTGTTTTTTTAGACAG__TCTCACTCTGTTGCTCAGGCTGGAGTGCAGTG ATT A ZUP1 Ensembl:ENSG00000153975 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1365283971 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_241103,RMVar_hsa_circ_299784,RMVar_hsa_circ_325730,RMVar_hsa_circ_313488,RMVar_hsa_circ_282023,RMVar_hsa_circ_241101,RMVar_hsa_circ_241102 7544 RMVar_ID_7544 Human_SNP_ID_293200388 A-to-I Human chr6 - 116647350 116647350 116647350 TTTTTGTTTGTTTGTTTGTTTTTTTAGACAGAATCTCACTCTGTTGCTCAGGCTGGAGTGCAGTG TTTTTGTTTGTTTGTTTGTTTTTTTAGACAGAGTCTCACTCTGTTGCTCAGGCTGGAGTGCAGTG T C ZUP1 Ensembl:ENSG00000153975 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6568959 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_452,GWAS_ID_453,GWAS_ID_454,GWAS_ID_455,GWAS_ID_456,GWAS_ID_457,GWAS_ID_458,GWAS_ID_459,GWAS_ID_460,GWAS_ID_461,GWAS_ID_462,GWAS_ID_463,GWAS_ID_464,GWAS_ID_465,GWAS_ID_466,GWAS_ID_467,GWAS_ID_468,GWAS_ID_469,GWAS_ID_470,GWAS_ID_471,GWAS_ID_472,GWAS_ID_473,GWAS_ID_474,GWAS_ID_475,GWAS_ID_476,GWAS_ID_477,GWAS_ID_478,GWAS_ID_479,GWAS_ID_480,GWAS_ID_481,GWAS_ID_482,GWAS_ID_483,GWAS_ID_484,GWAS_ID_485,GWAS_ID_486,GWAS_ID_487,GWAS_ID_488,GWAS_ID_489,GWAS_ID_490,GWAS_ID_491,GWAS_ID_492,GWAS_ID_493,GWAS_ID_494,GWAS_ID_495,GWAS_ID_496,GWAS_ID_497,GWAS_ID_498,GWAS_ID_499,GWAS_ID_500,GWAS_ID_501,GWAS_ID_502,GWAS_ID_503,GWAS_ID_504,GWAS_ID_505,GWAS_ID_506,GWAS_ID_507,GWAS_ID_508,GWAS_ID_509,GWAS_ID_510,GWAS_ID_511,GWAS_ID_512,GWAS_ID_513,GWAS_ID_514,GWAS_ID_515,GWAS_ID_516,GWAS_ID_517,GWAS_ID_518,GWAS_ID_519,GWAS_ID_520,GWAS_ID_521,GWAS_ID_522,GWAS_ID_523,GWAS_ID_524,GWAS_ID_525,GWAS_ID_526,GWAS_ID_527,GWAS_ID_528,GWAS_ID_529,GWAS_ID_530,GWAS_ID_531,GWAS_ID_532,GWAS_ID_533,GWAS_ID_534,GWAS_ID_535,GWAS_ID_536,GWAS_ID_537,GWAS_ID_538,GWAS_ID_539,GWAS_ID_540,GWAS_ID_541,GWAS_ID_542,GWAS_ID_543,GWAS_ID_544,GWAS_ID_545,GWAS_ID_546,GWAS_ID_547,GWAS_ID_548,GWAS_ID_549,GWAS_ID_550,GWAS_ID_551,GWAS_ID_552,GWAS_ID_553,GWAS_ID_554,GWAS_ID_555,GWAS_ID_556,GWAS_ID_557,GWAS_ID_558,GWAS_ID_559,GWAS_ID_560,GWAS_ID_561,GWAS_ID_562,GWAS_ID_563,GWAS_ID_564,GWAS_ID_565,GWAS_ID_566,GWAS_ID_567,GWAS_ID_568,GWAS_ID_569,GWAS_ID_570,GWAS_ID_571,GWAS_ID_572,GWAS_ID_573,GWAS_ID_574,GWAS_ID_575,GWAS_ID_576,GWAS_ID_577,GWAS_ID_578,GWAS_ID_579,GWAS_ID_580,GWAS_ID_581,GWAS_ID_582,GWAS_ID_583,GWAS_ID_584,GWAS_ID_585,GWAS_ID_586,GWAS_ID_587,GWAS_ID_588,GWAS_ID_589,GWAS_ID_590,GWAS_ID_591,GWAS_ID_592,GWAS_ID_593,GWAS_ID_594,GWAS_ID_595,GWAS_ID_596,GWAS_ID_597,GWAS_ID_598,GWAS_ID_599,GWAS_ID_600,GWAS_ID_601,GWAS_ID_602,GWAS_ID_603,GWAS_ID_604,GWAS_ID_605,GWAS_ID_606,GWAS_ID_607,GWAS_ID_608,GWAS_ID_609,GWAS_ID_610,GWAS_ID_611,GWAS_ID_612,GWAS_ID_613,GWAS_ID_614,GWAS_ID_615,GWAS_ID_616,GWAS_ID_617,GWAS_ID_618,GWAS_ID_619,GWAS_ID_620 RMVar_hsa_circ_241103,RMVar_hsa_circ_299784,RMVar_hsa_circ_325730,RMVar_hsa_circ_313488,RMVar_hsa_circ_282023,RMVar_hsa_circ_241101,RMVar_hsa_circ_241102 7545 RMVar_ID_7545 Human_SNP_ID_293339452 A-to-I Human chr6 - 117220093 117220093 117220093 GGGTAAAACCCATAGCAAGAGGTGAGCCTATTATTATATATGCCCCTTGGACAAAGACTGAACTT GGGTAAAACCCATAGCAAGAGGTGAGCCTATTGTTATATATGCCCCTTGGACAAAGACTGAACTT T C AB755814 RNACentral:URS000042AFE7 antisense RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1294310154 Functional Loss SNV dbSNP153 33..33 33 - - - 7546 RMVar_ID_7546 Human_SNP_ID_293423283 A-to-I Human chr6 - 117564102 117564102 117564102 ATGGTGGCACATGCTTGTAGCTCCAGCTACTCAGGAGGCTGAGGTGGAAGGATTGCTTGAGCCTA ATGGTGGCACATGCTTGTAGCTCCAGCTACTCGGGAGGCTGAGGTGGAAGGATTGCTTGAGCCTA T C AL132671.2,GOPC Ensembl:ENSG00000282218,Ensembl:ENSG00000047932 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1314131536 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17576437 RMVar_hsa_circ_80795,RMVar_hsa_circ_105935,RMVar_hsa_circ_241142,RMVar_hsa_circ_241143 7547 RMVar_ID_7547 Human_SNP_ID_293444894 A-to-I Human chr6 - 117658858 117658858 117658858 TCGGACTCAGCCCGCCTGCACTCAGGTGAAATAAACAGCCATGTTGCTCACAGAAAGCCTGTTTG TCGGACTCAGCCCGCCTGCACTCAGGTGAAATGAACAGCCATGTTGCTCACAGAAAGCCTGTTTG T C LOC101927919,LOC101927919:2,LOC101927919:3,LOC101927919:4,LOC101927919:5,LOC101927919:6,piR-32559 RNACentral:URS0000D6D4AE,RNACentral:URS0000D6DCC7,RNACentral:URS0000D6E930,RNACentral:URS0000D6D754,RNACentral:URS0000D5C35D,RNACentral:URS0000D5A46A,RNACentral:URS0000616DEF lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,piRNA intron,intron,intron,intron,intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1477200487 Functional Loss SNV dbSNP153 33..33 33 - - - 7548 RMVar_ID_7548 Human_SNP_ID_293444947 A-to-I Human chr6 - 117659057 117659057 117659057 TTCTGCCCTACCCTAACTGATCAATGTTCTTTATAATCTCTCCGACCCTTAAGAAGTTTCTTTGT TTCTGCCCTACCCTAACTGATCAATGTTCTTTCTAATCTCTCCGACCCTTAAGAAGTTTCTTTGT T G LOC101927919,LOC101927919:2,LOC101927919:3,LOC101927919:4,LOC101927919:5,LOC101927919:6 RNACentral:URS0000D6D4AE,RNACentral:URS0000D6DCC7,RNACentral:URS0000D6E930,RNACentral:URS0000D6D754,RNACentral:URS0000D5C35D,RNACentral:URS0000D5A46A lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs577768167 Functional Loss SNV dbSNP153 33..33 33 - - - 7549 RMVar_ID_7549 Human_SNP_ID_293451615 A-to-I Human chr6 + 117685488 117685488 117685488 GCAGCCTTGAACTCCTGGGCAGCCTCCTGAGTAGGTTGTACTACAGGCACAAGCCACCATGCCTG GCAGCCTTGAACTCCTGGGCAGCCTCCTGAGTGGGTTGTACTACAGGCACAAGCCACCATGCCTG A G NUS1 Ensembl:ENSG00000153989 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs964709094 Functional Loss SNV dbSNP153 33..33 33 - - - 7550 RMVar_ID_7550 Human_SNP_ID_293732883 A-to-I Human chr6 - 118853582 118853582 118853582 TTGCCCAGGCTGGTCTCAAATTCTTGGGCTCAAATGTTCCACTTGCCTCGGCCTTTCAGAGCACT TTGCCCAGGCTGGTCTCAAATTCTTGGGCTCAGATGTTCCACTTGCCTCGGCCTTTCAGAGCACT T C MCM9 Ensembl:ENSG00000111877 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1010082262 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3367,RMVar_hsa_circ_241179,RMVar_hsa_circ_334432,RMVar_hsa_circ_241181,RMVar_hsa_circ_241183,RMVar_hsa_circ_302558,RMVar_hsa_circ_241184 7551 RMVar_ID_7551 Human_SNP_ID_293746541 A-to-I Human chr6 - 118910824 118910824 118910824 TACAACAGAAAATGGCCAATTAATGGTCCTGTATAAGTGGAAAACTGTTAAGGAGGTCTCAGGTT TACAACAGAAAATGGCCAATTAATGGTCCTGTGTAAGTGGAAAACTGTTAAGGAGGTCTCAGGTT T C MCM9 Ensembl:ENSG00000111877 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs762251186 Functional Loss SNV dbSNP153 33..33 33 - - - 7552 RMVar_ID_7552 Human_SNP_ID_293752773 A-to-I Human chr6 + 118936057 118936057 118936057 GACTTACAGTTCAGCATGGCTGGGGAGACTTCAGGAAACTTAAAATCATGGCAGAAGCGGGAGCA GACTTACAGTTCAGCATGGCTGGGGAGACTTCGGGAAACTTAAAATCATGGCAGAAGCGGGAGCA A G AL137009.2 Ensembl:ENSG00000253194 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1260430010 Functional Loss SNV dbSNP153 33..33 33 - - - 7553 RMVar_ID_7553 Human_SNP_ID_293765339 A-to-I Human chr6 - 118991427 118991427 118991427 CGGGAACGGTGGCTCACACCTGTAATCCCAGCACTTTAGGAGGCCGAGGTAGGTGGATCTCATTT CGGGAACGGTGGCTCACACCTGTAATCCCAGCTCTTTAGGAGGCCGAGGTAGGTGGATCTCATTT T A FAM184A Ensembl:ENSG00000111879 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1463581748 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10502,RMVar_hsa_circ_15134,RMVar_hsa_circ_241186,RMVar_hsa_circ_11905,RMVar_hsa_circ_269656 7554 RMVar_ID_7554 Human_SNP_ID_293852624 A-to-I Human chr6 + 119357404 119357404 119357404 GAGTTTTGCTTTTGTGGTTCAGGCTGGAGTGCAATGGCATGATCTCGGCCCACTGCAACCTCTGC GAGTTTTGCTTTTGTGGTTCAGGCTGGAGTGCGATGGCATGATCTCGGCCCACTGCAACCTCTGC A G AL078600.1 Ensembl:ENSG00000287100 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1377281359 Functional Loss SNV dbSNP153 33..33 33 - - - 7555 RMVar_ID_7555 Human_SNP_ID_430821174 A-to-I Human chr10 + 45430518 45430517 45430518 CAGGCACCATGGTGGTACACAACTGTAGTCCCAGCTACTTGAGAGGCTGAGGCAGGAGGCTCACT CAGGCACCATGGTGGTACACAACTGTAGTCCC_GCTACTTGAGAGGCTGAGGCAGGAGGCTCACT CA C ALOX5 Ensembl:ENSG00000012779 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1228744991 Functional Loss DEL dbSNP153 33..33 33 - - - 7556 RMVar_ID_7556 Human_SNP_ID_430866306 A-to-I Human chr10 - 45619177 45619177 45619177 AAAAAAAGCTGAGCGTGGTGGTGCGTGCCCATAGTCCCAGCTACTCGGGAGGCTGAGGCAGAAGA AAAAAAAGCTGAGCGTGGTGGTGCGTGCCCATGGTCCCAGCTACTCGGGAGGCTGAGGCAGAAGA T C ZFAND4 Ensembl:ENSG00000172671 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1315659997 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13729,RMVar_hsa_circ_350397 7557 RMVar_ID_7557 Human_SNP_ID_430866307 A-to-I Human chr10 - 45619179 45619179 45619179 AAAAAAAAAGCTGAGCGTGGTGGTGCGTGCCCATAGTCCCAGCTACTCGGGAGGCTGAGGCAGAA AAAAAAAAAGCTGAGCGTGGTGGTGCGTGCCCGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGAA T C ZFAND4 Ensembl:ENSG00000172671 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1287073609 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13729,RMVar_hsa_circ_350397 7558 RMVar_ID_7558 Human_SNP_ID_430866529 A-to-I Human chr10 - 45620223 45620223 45620223 CACCTTGGCCTCCCAAAGTGCTAGGATTACAGATGTGAGCCACCGCGCCCAGCCTCACAAGAGTT CACCTTGGCCTCCCAAAGTGCTAGGATTACAGGTGTGAGCCACCGCGCCCAGCCTCACAAGAGTT T C ZFAND4 Ensembl:ENSG00000172671 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10736836 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13729,RMVar_hsa_circ_350397 7559 RMVar_ID_7559 Human_SNP_ID_430866533 A-to-I Human chr10 - 45620233 45620233 45620233 TTGATTCGCCCACCTTGGCCTCCCAAAGTGCTAGGATTACAGATGTGAGCCACCGCGCCCAGCCT TTGATTCGCCCACCTTGGCCTCCCAAAGTGCTGGGATTACAGATGTGAGCCACCGCGCCCAGCCT T C ZFAND4 Ensembl:ENSG00000172671 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1415816121 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13729,RMVar_hsa_circ_350397 7560 RMVar_ID_7560 Human_SNP_ID_430869002 A-to-I Human chr10 - 45629741 45629741 45629741 CTCCCACCTCAGCCTCCCAAGTAGCTGGGACTACGGGCTCCTGCCACCATGCCCAGCTAATTTTT CTCCCACCTCAGCCTCCCAAGTAGCTGGGACTTCGGGCTCCTGCCACCATGCCCAGCTAATTTTT T A ZFAND4 Ensembl:ENSG00000172671 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs763071143 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55587,RMVar_hsa_circ_75387,RMVar_hsa_circ_13729,RMVar_hsa_circ_350397,RMVar_hsa_circ_287346 7561 RMVar_ID_7561 Human_SNP_ID_430895296 A-to-I Human chr10 + 45728072 45728072 45728072 TTAAAAGGAGACAGGGTTTTGCCCTGTCGCCCAGGCTGGAGTGCAAGTGGCTCGATCTTGGCTCA TTAAAAGGAGACAGGGTTTTGCCCTGTCGCCCCGGCTGGAGTGCAAGTGGCTCGATCTTGGCTCA A C WASHC2C Ensembl:ENSG00000172661 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1483098227 Functional Loss SNV dbSNP153 33..33 33 - - - 7562 RMVar_ID_7562 Human_SNP_ID_430895334 A-to-I Human chr10 + 45728290 45728290 45728290 GGACTCTAGCGATAACCCTGCCTCAGCCTCCCAAAGTGTTGGATTACAAGCGTGAGCCACCATAC GGACTCTAGCGATAACCCTGCCTCAGCCTCCCGAAGTGTTGGATTACAAGCGTGAGCCACCATAC A G WASHC2C Ensembl:ENSG00000172661 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs553222839 Functional Loss SNV dbSNP153 33..33 33 - - - 7563 RMVar_ID_7563 Human_SNP_ID_430927604 A-to-I Human chr10 - 45852140 45852140 45852140 TGGGAGGCCGAGGCGGGCAGATCACGAAGTCAAGAGACGGAGACCATCCTGCCTAACACGTTGAA TGGGAGGCCGAGGCGGGCAGATCACGAAGTCAGGAGACGGAGACCATCCTGCCTAACACGTTGAA T C AGAP4 Ensembl:ENSG00000188234 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1265531033 Functional Loss SNV dbSNP153 33..33 33 - - - 7564 RMVar_ID_7564 Human_SNP_ID_430927607 A-to-I Human chr10 - 45852154 45852154 45852154 GTAATCCCAGACTGTGGGAGGCCGAGGCGGGCAGATCACGAAGTCAAGAGACGGAGACCATCCTG GTAATCCCAGACTGTGGGAGGCCGAGGCGGGCGGATCACGAAGTCAAGAGACGGAGACCATCCTG T C AGAP4 Ensembl:ENSG00000188234 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1289800711 Functional Loss SNV dbSNP153 33..33 33 - - - 7565 RMVar_ID_7565 Human_SNP_ID_430957634 A-to-I Human chr10 + 45994573 45994573 45994573 GTGATGCTCCCATCTCAGCCTCCCAAGATGCTAGGACTACAGGCACACGCCACCATGCCTGGCTA GTGATGCTCCCATCTCAGCCTCCCAAGATGCTGGGACTACAGGCACACGCCACCATGCCTGGCTA A G TIMM23 Ensembl:ENSG00000265354 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1429573914 Functional Loss SNV dbSNP153 33..33 33 - - - 7566 RMVar_ID_7566 Human_SNP_ID_430957637 A-to-I Human chr10 + 45994579 45994579 45994579 CTCCCATCTCAGCCTCCCAAGATGCTAGGACTACAGGCACACGCCACCATGCCTGGCTAATTTTT CTCCCATCTCAGCCTCCCAAGATGCTAGGACTGCAGGCACACGCCACCATGCCTGGCTAATTTTT A G TIMM23 Ensembl:ENSG00000265354 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1453901144 Functional Loss SNV dbSNP153 33..33 33 - - - 7567 RMVar_ID_7567 Human_SNP_ID_430960671 A-to-I Human chr10 + 46005848 46005848 46005848 TTAGTCGGTACTGGGGTTCTTTTAAGCCCCGTAGGTCTGTAGAATATTTTAAAAGGCTAGAATTA TTAGTCGGTACTGGGGTTCTTTTAAGCCCCGTGGGTCTGTAGAATATTTTAAAAGGCTAGAATTA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1378955315 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5974511,Human_RBP_ID_11369984 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 7568 RMVar_ID_7568 Human_SNP_ID_430961252 A-to-I Human chr10 + 46007692 46007692 46007692 ATAGCACACTGCAGCCTTGACCTCCCAGACACAAGATTCTCCCACCTCAGCCTCCTGAGTAGCTG ATAGCACACTGCAGCCTTGACCTCCCAGACACCAGATTCTCCCACCTCAGCCTCCTGAGTAGCTG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1554920162 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5974449,Human_RBP_ID_11369939 RMVar_hsa_circ_96127,RMVar_hsa_circ_143390,RMVar_hsa_circ_143394,RMVar_hsa_circ_143384,RMVar_hsa_circ_143389,RMVar_hsa_circ_119392,RMVar_hsa_circ_87154,RMVar_hsa_circ_82047 7569 RMVar_ID_7569 Human_SNP_ID_430961289 A-to-I Human chr10 + 46007823 46007823 46007823 GTTGCCCAGGCTGGTGTTAAACTCCTTGGCTCAAGCAATCTTCCTACCTCTGCCTCCCAAAGTGC GTTGCCCAGGCTGGTGTTAAACTCCTTGGCTCGAGCAATCTTCCTACCTCTGCCTCCCAAAGTGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1188662675 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17777963 RMVar_hsa_circ_96127,RMVar_hsa_circ_143390,RMVar_hsa_circ_143394,RMVar_hsa_circ_143384,RMVar_hsa_circ_143389,RMVar_hsa_circ_119392,RMVar_hsa_circ_87154,RMVar_hsa_circ_82047 7570 RMVar_ID_7570 Human_SNP_ID_431069016 A-to-I Human chr10 + 46449697 46449697 46449697 TCCTTGGAACCCATGATCCTCACTGTACAAACATGGAAACTGAGACCAAGGACTATGAGACAGTG TCCTTGGAACCCATGATCCTCACTGTACAAACGTGGAAACTGAGACCAAGGACTATGAGACAGTG A G LINC00842,AC244230.2 Ensembl:ENSG00000285294,Ensembl:ENSG00000285402 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202426802 Functional Loss SNV dbSNP153 33..33 33 - - - 7571 RMVar_ID_7571 Human_SNP_ID_431070348 A-to-I Human chr10 + 46455705 46455705 46455705 AAAAAGAAAAAAAAAGATTTAATTTTTTAATTAGCTGGACATGGTGGTATGCACCTGTGGTGCTA AAAAAGAAAAAAAAAGATTTAATTTTTTAATTTGCTGGACATGGTGGTATGCACCTGTGGTGCTA A T AC244230.2 Ensembl:ENSG00000285402 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1385787619 Functional Loss SNV dbSNP153 33..33 33 - - - 7572 RMVar_ID_7572 Human_SNP_ID_431070883 A-to-I Human chr10 + 46458534 46458534 46458534 AGGCAGAAGCTGCAGTGAGCCAAGATCGTGCCATTGCACTCCAGCCTGGGCAGCATGAGTGAAAC AGGCAGAAGCTGCAGTGAGCCAAGATCGTGCCTTTGCACTCCAGCCTGGGCAGCATGAGTGAAAC A T AC244230.2 Ensembl:ENSG00000285402 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1199050920 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2218396 7573 RMVar_ID_7573 Human_SNP_ID_431110112 A-to-I Human chr10 - 46591271 46591271 46591271 TCACTTCAGCCTTAACCTCCCGGGCTCACGCAATACTCCTGCCCCAGCCCTCCAAGTAGCTGGGA TCACTTCAGCCTTAACCTCCCGGGCTCACGCAGTACTCCTGCCCCAGCCCTCCAAGTAGCTGGGA T C AL356056.2 Ensembl:ENSG00000231187 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1289967613 Functional Loss SNV dbSNP153 33..33 33 - - - 7574 RMVar_ID_7574 Human_SNP_ID_431118582 A-to-I Human chr10 - 46634242 46634242 46634242 AATTTATTTTTTAGAGACAGGATCTCACTGTTACCCAGGCTGGAGTGCAGTGGTCTGATCATAGC AATTTATTTTTTAGAGACAGGATCTCACTGTTCCCCAGGCTGGAGTGCAGTGGTCTGATCATAGC T G SHLD2P1 Ensembl:ENSG00000165874 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1274185292 Functional Loss SNV dbSNP153 33..33 33 - - - 7575 RMVar_ID_7575 Human_SNP_ID_431152624 A-to-I Human chr10 + 46809430 46809430 46809430 TTTTTTTTAGTGGAGACGAGGTTTCACTATGTAAGTGAAGCTGGTCTCGAACTCCTGACCTCAGA TTTTTTTTAGTGGAGACGAGGTTTCACTATGTTAGTGAAGCTGGTCTCGAACTCCTGACCTCAGA A T BMS1P1 Ensembl:ENSG00000204177 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1435384249 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11485030 7576 RMVar_ID_7576 Human_SNP_ID_431410814 A-to-I Human chr10 - 48046737 48046737 48046737 AAAACATTGGCTGGGCATGGTGGCTCATTCCTATAGTTCAGGCTACTCAGGAGCCTGAGGTAGGA AAAACATTGGCTGGGCATGGTGGCTCATTCCTGTAGTTCAGGCTACTCAGGAGCCTGAGGTAGGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1320758023 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17346981 7577 RMVar_ID_7577 Human_SNP_ID_431465405 A-to-I Human chr10 + 48313396 48313396 48313396 CGGAGGTTGCAGTGAGCTGAGATCGTGCCACTACACTCCAGCCTGGGCGGCAGAGGTGTAGACTC CGGAGGTTGCAGTGAGCTGAGATCGTGCCACTGCACTCCAGCCTGGGCGGCAGAGGTGTAGACTC A G MAPK8 Ensembl:ENSG00000107643 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1186615156 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1261,RMVar_hsa_circ_311199,RMVar_hsa_circ_332922,RMVar_hsa_circ_315434,RMVar_hsa_circ_11781,RMVar_hsa_circ_51276,RMVar_hsa_circ_6086 7578 RMVar_ID_7578 Human_SNP_ID_431492555 A-to-I Human chr10 + 48421590 48421590 48421590 ACTTTGGGAGGCCGAGGCTCGTGGATCACTCGAGGCTAGGAGTTCTAGACCAGCCTGAGCAACAT ACTTTGGGAGGCCGAGGCTCGTGGATCACTCGCGGCTAGGAGTTCTAGACCAGCCTGAGCAACAT A C MAPK8 Ensembl:ENSG00000107643 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1466891561 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1261,RMVar_hsa_circ_11781,RMVar_hsa_circ_51276,RMVar_hsa_circ_5515,RMVar_hsa_circ_16977,RMVar_hsa_circ_61034,RMVar_hsa_circ_325786,RMVar_hsa_circ_332690,RMVar_hsa_circ_143348,RMVar_hsa_circ_11229,RMVar_hsa_circ_48543,RMVar_hsa_circ_46855,RMVar_hsa_circ_348214,RMVar_hsa_circ_301759,RMVar_hsa_circ_143352 7579 RMVar_ID_7579 Human_SNP_ID_431588392 A-to-I Human chr10 + 48799941 48799941 48799941 CAGAGTCTCACTCTGTTGCCAGACCGGAGTGCAGTGGCACAATCTCGGCTCACAGCAACCTCTGT CAGAGTCTCACTCTGTTGCCAGACCGGAGTGCGGTGGCACAATCTCGGCTCACAGCAACCTCTGT A G WDFY4 Ensembl:ENSG00000128815 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1263862549 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 7580 RMVar_ID_7580 Human_SNP_ID_431755466 A-to-I Human chr10 - 49438520 49438520 49438520 TCCCCTCCCAAATGTTGCATTGTAGCTCCCAGAATTCCCATGTGCTGTGGGAGGGACCCAGTGGG TCCCCTCCCAAATGTTGCATTGTAGCTCCCAGGATTCCCATGTGCTGTGGGAGGGACCCAGTGGG T C lnc-ERCC6-1 RNACentral:URS00008BE7F7 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042846308 Functional Loss SNV dbSNP153 33..33 33 - - - 7581 RMVar_ID_7581 Human_SNP_ID_431776273 A-to-I Human chr10 - 49525534 49525534 49525534 TTATGTGGTAATTTTGCCAGAGATGAATTTCAACTAATGAAAGAGGGATACTTTCTGGTGACTTT TTATGTGGTAATTTTGCCAGAGATGAATTTCAGCTAATGAAAGAGGGATACTTTCTGGTGACTTT T C ERCC6 Ensembl:ENSG00000225830 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs759944917 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267720,RMVar_hsa_circ_23428,RMVar_hsa_circ_68698,RMVar_hsa_circ_143370,RMVar_hsa_circ_361236,RMVar_hsa_circ_315857 7582 RMVar_ID_7582 Human_SNP_ID_431776274 A-to-I Human chr10 - 49525540 49525540 49525540 TTTTGGTTATGTGGTAATTTTGCCAGAGATGAATTTCAACTAATGAAAGAGGGATACTTTCTGGT TTTTGGTTATGTGGTAATTTTGCCAGAGATGAGTTTCAACTAATGAAAGAGGGATACTTTCTGGT T C ERCC6 Ensembl:ENSG00000225830 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1382699241 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267720,RMVar_hsa_circ_23428,RMVar_hsa_circ_68698,RMVar_hsa_circ_143370,RMVar_hsa_circ_361236,RMVar_hsa_circ_315857 7583 RMVar_ID_7583 Human_SNP_ID_431881576 A-to-I Human chr10 + 49963795 49963795 49963795 CAAGACCAGCCTGGCCAACATGATGAAACCCCATCTCTACTAAAATACAAAAACTAGCCGGGCAT CAAGACCAGCCTGGCCAACATGATGAAACCCCGTCTCTACTAAAATACAAAAACTAGCCGGGCAT A G TIMM23B-AGAP6,TIMM23B Ensembl:ENSG00000178440,Ensembl:ENSG00000204152 lincRNA,Pseudogene intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1268634554 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_274469,RMVar_hsa_circ_273667,RMVar_hsa_circ_329752,RMVar_hsa_circ_297312 7584 RMVar_ID_7584 Human_SNP_ID_431881577 A-to-I Human chr10 + 49963795 49963795 49963795 CAAGACCAGCCTGGCCAACATGATGAAACCCCATCTCTACTAAAATACAAAAACTAGCCGGGCAT CAAGACCAGCCTGGCCAACATGATGAAACCCCTTCTCTACTAAAATACAAAAACTAGCCGGGCAT A T TIMM23B-AGAP6,TIMM23B Ensembl:ENSG00000178440,Ensembl:ENSG00000204152 lincRNA,Pseudogene intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1268634554 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_274469,RMVar_hsa_circ_273667,RMVar_hsa_circ_329752,RMVar_hsa_circ_297312 7585 RMVar_ID_7585 Human_SNP_ID_431882501 A-to-I Human chr10 + 49966671 49966668 49966672 AACATGATGAAACCCCATCTCTACTAAAATAAAAAAACTAGCCGGGCATGATAGCGGGTGCCTGT AACATGATGAAACCCCATCTCTACTAAAAT____AAACTAGCCGGGCATGATAGCGGGTGCCTGT TAAAA T TIMM23B-AGAP6,TIMM23B Ensembl:ENSG00000178440,Ensembl:ENSG00000204152 lincRNA,Pseudogene intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170500622 Functional Loss DEL dbSNP153 31..34 33 - - - RMVar_hsa_circ_274469,RMVar_hsa_circ_273667,RMVar_hsa_circ_329752,RMVar_hsa_circ_297312 7586 RMVar_ID_7586 Human_SNP_ID_431882502 A-to-I Human chr10 + 49966671 49966668 49966672 AACATGATGAAACCCCATCTCTACTAAAATAAAAAAACTAGCCGGGCATGATAGCGGGTGCCTGT AACATGATGAAACCCCATCTCTACTAAAATA___AAACTAGCCGGGCATGATAGCGGGTGCCTGT TAAAA TA TIMM23B-AGAP6,TIMM23B Ensembl:ENSG00000178440,Ensembl:ENSG00000204152 lincRNA,Pseudogene intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170500622 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_274469,RMVar_hsa_circ_273667,RMVar_hsa_circ_329752,RMVar_hsa_circ_297312 7587 RMVar_ID_7587 Human_SNP_ID_431882506 A-to-I Human chr10 + 49966671 49966671 49966671 AACATGATGAAACCCCATCTCTACTAAAATAAAAAAACTAGCCGGGCATGATAGCGGGTGCCTGT AACATGATGAAACCCCATCTCTACTAAAATAATAAAACTAGCCGGGCATGATAGCGGGTGCCTGT A T TIMM23B-AGAP6,TIMM23B Ensembl:ENSG00000178440,Ensembl:ENSG00000204152 lincRNA,Pseudogene intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1192310047 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_274469,RMVar_hsa_circ_273667,RMVar_hsa_circ_329752,RMVar_hsa_circ_297312 7588 RMVar_ID_7588 Human_SNP_ID_431882509 A-to-I Human chr10 + 49966678 49966678 49966678 TGAAACCCCATCTCTACTAAAATAAAAAAACTAGCCGGGCATGATAGCGGGTGCCTGTAATCCCA TGAAACCCCATCTCTACTAAAATAAAAAAACTGGCCGGGCATGATAGCGGGTGCCTGTAATCCCA A G TIMM23B-AGAP6,TIMM23B Ensembl:ENSG00000178440,Ensembl:ENSG00000204152 lincRNA,Pseudogene intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1211253700 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_274469,RMVar_hsa_circ_273667,RMVar_hsa_circ_329752,RMVar_hsa_circ_297312 7589 RMVar_ID_7589 Human_SNP_ID_431882625 A-to-I Human chr10 + 49967045 49967045 49967045 GGGTTCAAGTGATGCTCCCATCTCAACCTCCCAAGATGCTAGGACTACAGGCACATGCCACCATG GGGTTCAAGTGATGCTCCCATCTCAACCTCCCCAGATGCTAGGACTACAGGCACATGCCACCATG A C TIMM23B-AGAP6,TIMM23B Ensembl:ENSG00000178440,Ensembl:ENSG00000204152 lincRNA,Pseudogene intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1554855549 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_274469,RMVar_hsa_circ_273667,RMVar_hsa_circ_329752,RMVar_hsa_circ_297312 7590 RMVar_ID_7590 Human_SNP_ID_431882635 A-to-I Human chr10 + 49967085 49967085 49967085 AGGACTACAGGCACATGCCACCATGCCTGGCTAATTTTTTTGTGTTTTTTGTAGAGACAGGGTTT AGGACTACAGGCACATGCCACCATGCCTGGCTGATTTTTTTGTGTTTTTTGTAGAGACAGGGTTT A G TIMM23B-AGAP6,TIMM23B Ensembl:ENSG00000178440,Ensembl:ENSG00000204152 lincRNA,Pseudogene intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1310759740 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11370225 RMVar_hsa_circ_274469,RMVar_hsa_circ_273667,RMVar_hsa_circ_329752,RMVar_hsa_circ_297312 7591 RMVar_ID_7591 Human_SNP_ID_431882995 A-to-I Human chr10 + 49968585 49968585 49968585 GGCCTGGCACAGTGGCTCATGTCTGTAATCCCAGCACTTTGGGAGTCCAAGGCGGGAGGATCACA GGCCTGGCACAGTGGCTCATGTCTGTAATCCCGGCACTTTGGGAGTCCAAGGCGGGAGGATCACA A G TIMM23B-AGAP6,TIMM23B Ensembl:ENSG00000178440,Ensembl:ENSG00000204152 lincRNA,Pseudogene intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1471494276 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_274469,RMVar_hsa_circ_273667,RMVar_hsa_circ_329752,RMVar_hsa_circ_297312 7592 RMVar_ID_7592 Human_SNP_ID_431883003 A-to-I Human chr10 + 49968615 49968615 49968615 CCAGCACTTTGGGAGTCCAAGGCGGGAGGATCACAAGGTCAGGAGATTGAGACCATCCTGGCTAA CCAGCACTTTGGGAGTCCAAGGCGGGAGGATCTCAAGGTCAGGAGATTGAGACCATCCTGGCTAA A T TIMM23B-AGAP6,TIMM23B Ensembl:ENSG00000178440,Ensembl:ENSG00000204152 lincRNA,Pseudogene intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1267763247 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_274469,RMVar_hsa_circ_273667,RMVar_hsa_circ_329752,RMVar_hsa_circ_297312 7593 RMVar_ID_7593 Human_SNP_ID_431884363 A-to-I Human chr10 + 49973420 49973420 49973420 TCCAGTTGCTGGGCACAATGGTTCACACCTGTAATCTCAGCACGTTTGGAGGGCAAGGCAGGAGG TCCAGTTGCTGGGCACAATGGTTCACACCTGTCATCTCAGCACGTTTGGAGGGCAAGGCAGGAGG A C TIMM23B-AGAP6,TIMM23B Ensembl:ENSG00000178440,Ensembl:ENSG00000204152 lincRNA,Pseudogene intron,exon GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1297320654 Functional Loss SNV dbSNP153 33..33 33 - - - 7594 RMVar_ID_7594 Human_SNP_ID_431884495 A-to-I Human chr10 + 49973999 49973999 49973999 AATTTTTTGTGTTTTAGTAGAGACGGGGTTTTACCATGTTGGCCAGGATGGTCTCGATCCCCCGA AATTTTTTGTGTTTTAGTAGAGACGGGGTTTTGCCATGTTGGCCAGGATGGTCTCGATCCCCCGA A G TIMM23B-AGAP6,TIMM23B Ensembl:ENSG00000178440,Ensembl:ENSG00000204152 lincRNA,Pseudogene intron,exon GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1485751167 Functional Loss SNV dbSNP153 33..33 33 - - - 7595 RMVar_ID_7595 Human_SNP_ID_431886606 A-to-I Human chr10 + 49981434 49981434 49981434 TCTCTGTCTCTCTCTCTCTTTTTTTTTTTTTGAGAGGGAGTCTCACTCTGTCGCCCAGGCTGGAG TCTCTGTCTCTCTCTCTCTTTTTTTTTTTTTGCGAGGGAGTCTCACTCTGTCGCCCAGGCTGGAG A C TIMM23B-AGAP6 Ensembl:ENSG00000178440 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1288896230 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2219983,Human_RBP_ID_11370341 7596 RMVar_ID_7596 Human_SNP_ID_431886651 A-to-I Human chr10 + 49981605 49981605 49981605 CCCGGCTAATTTTTGTGATTTTTTTTTTTAGTAGAGATGAGGTTTTACTATGTAGGCGAAGTTGG CCCGGCTAATTTTTGTGATTTTTTTTTTTAGTGGAGATGAGGTTTTACTATGTAGGCGAAGTTGG A G TIMM23B-AGAP6 Ensembl:ENSG00000178440 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444005265 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11370343,Human_RBP_ID_22881791 7597 RMVar_ID_7597 Human_SNP_ID_431886653 A-to-I Human chr10 + 49981622 49981622 49981622 ATTTTTTTTTTTAGTAGAGATGAGGTTTTACTATGTAGGCGAAGTTGGTCTCGAACTCCTGACCT ATTTTTTTTTTTAGTAGAGATGAGGTTTTACTGTGTAGGCGAAGTTGGTCTCGAACTCCTGACCT A G TIMM23B-AGAP6 Ensembl:ENSG00000178440 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256800276 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2219984,Human_RBP_ID_11370347 7598 RMVar_ID_7598 Human_SNP_ID_431890081 A-to-I Human chr10 + 49993709 49993709 49993709 AGGCATGGTGGCATGTGCCTGTACTCCCAGCTAATCAGGAGGCTAAGGCTGAAGAATTGGTTGAA AGGCATGGTGGCATGTGCCTGTACTCCCAGCTTATCAGGAGGCTAAGGCTGAAGAATTGGTTGAA A T TIMM23B-AGAP6,AGAP6 Ensembl:ENSG00000178440,Ensembl:ENSG00000204149 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1554861509 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120567,RMVar_hsa_circ_378399,RMVar_hsa_circ_143399,RMVar_hsa_circ_108890,RMVar_hsa_circ_143400,RMVar_hsa_circ_143398,RMVar_hsa_circ_269000 7599 RMVar_ID_7599 Human_SNP_ID_431914856 A-to-I Human chr10 + 50087885 50087885 50087885 TTGTCCAGGCTGGAGTGCCGTGGCATGATCTCAGCTCACTGCAACCTCCGCCTCCTGGGTTCAAA TTGTCCAGGCTGGAGTGCCGTGGCATGATCTCGGCTCACTGCAACCTCCGCCTCCTGGGTTCAAA A G WASHC2A Ensembl:ENSG00000099290 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1487884447 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72003,RMVar_hsa_circ_143405,RMVar_hsa_circ_100726,RMVar_hsa_circ_355925,RMVar_hsa_circ_364223,RMVar_hsa_circ_368912,RMVar_hsa_circ_359328,RMVar_hsa_circ_55855,RMVar_hsa_circ_62991,RMVar_hsa_circ_54261,RMVar_hsa_circ_44619,RMVar_hsa_circ_86280,RMVar_hsa_circ_111034,RMVar_hsa_circ_143409,RMVar_hsa_circ_143410 7600 RMVar_ID_7600 Human_SNP_ID_431976684 A-to-I Human chr10 - 50365866 50365866 50365866 GCACACATGTTTATTGCAGTACCATTTACAATAGCAAAGACATGGAACCAACCCAAATGCCCATC GCACACATGTTTATTGCAGTACCATTTACAATGGCAAAGACATGGAACCAACCCAAATGCCCATC T C SGMS1 Ensembl:ENSG00000198964 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs565364746 Functional Loss SNV dbSNP153 33..33 33 - - - 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 7601 RMVar_ID_7601 Human_SNP_ID_431976687 A-to-I Human chr10 - 50365892 50365890 50365892 TAAATCATTCTAGTATAAAGACACATGCACACATGTTTATTGCAGTACCATTTACAATAGCAAAG TAAATCATTCTAGTATAAAGACACATGCACAC__GTTTATTGCAGTACCATTTACAATAGCAAAG CAT C SGMS1 Ensembl:ENSG00000198964 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1165474481 Functional Loss DEL dbSNP153 33..34 33 - - - 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 7602 RMVar_ID_7602 Human_SNP_ID_431981106 A-to-I Human chr10 - 50384723 50384723 50384723 AAAGTAGGCCGGGCACAGTGGGTCATGACAGTAATAACAGCACTTTGGGAGGCTGAGGCAAGAGG AAAGTAGGCCGGGCACAGTGGGTCATGACAGTCATAACAGCACTTTGGGAGGCTGAGGCAAGAGG T G SGMS1 Ensembl:ENSG00000198964 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1478449311 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11370671 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 7603 RMVar_ID_7603 Human_SNP_ID_432012490 A-to-I Human chr10 - 50528669 50528669 50528669 TTCTAGGGCTCCTGGACTCAAGCGATCCTTTCACCTTGGCTTCCCAAAGTGCTGGGATTACAGGT TTCTAGGGCTCCTGGACTCAAGCGATCCTTTCCCCTTGGCTTCCCAAAGTGCTGGGATTACAGGT T G SGMS1 Ensembl:ENSG00000198964 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1345269431 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115717,RMVar_hsa_circ_143420,RMVar_hsa_circ_111729,RMVar_hsa_circ_143421,RMVar_hsa_circ_25269,RMVar_hsa_circ_367186,RMVar_hsa_circ_271046,RMVar_hsa_circ_143426,RMVar_hsa_circ_278260,RMVar_hsa_circ_143432,RMVar_hsa_circ_143435,RMVar_hsa_circ_143433,RMVar_hsa_circ_119967,RMVar_hsa_circ_143434,RMVar_hsa_circ_143436,RMVar_hsa_circ_276645 7604 RMVar_ID_7604 Human_SNP_ID_432203922 A-to-I Human chr10 + 51335596 51335596 51335596 CTCTGTTCCCCAGGCTGGAGTGCAGTGGCACGATGTCGGCTTACTGCAAACTCGGCCTCCAAGGT CTCTGTTCCCCAGGCTGGAGTGCAGTGGCACGTTGTCGGCTTACTGCAAACTCGGCCTCCAAGGT A T PRKG1 Ensembl:ENSG00000185532 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1346875398 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8056829 7605 RMVar_ID_7605 Human_SNP_ID_432436586 A-to-I Human chr10 - 52290734 52290734 52290734 CTCCTGCTCCAGACTTTTGAGTAGTTAGGACTATAGGTGCACATCAGCACACCTGGCTAGTATTT CTCCTGCTCCAGACTTTTGAGTAGTTAGGACTTTAGGTGCACATCAGCACACCTGGCTAGTATTT T A PRKG1-AS1 Ensembl:ENSG00000236671 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1333508726 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_143454 7606 RMVar_ID_7606 Human_SNP_ID_433942920 A-to-I Human chr10 - 58205716 58205716 58205716 TCATCACCTGAGTAGCGTACATTGTACCTAATATGTAGTTTTTTAAATCCCTAGCCACCCTTCCC TCATCACCTGAGTAGCGTACATTGTACCTAATTTGTAGTTTTTTAAATCCCTAGCCACCCTTCCC T A IPMK Ensembl:ENSG00000151151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1364537689 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11378887 7607 RMVar_ID_7607 Human_SNP_ID_433956900 A-to-I Human chr10 - 58261746 58261746 58261746 AAAACCCTGTCTCTACAAAAAATGCAAAAATTAGCCGGATGTGTTGGTGGCGCCTATAGTCCCAG AAAACCCTGTCTCTACAAAAAATGCAAAAATTGGCCGGATGTGTTGGTGGCGCCTATAGTCCCAG T C IPMK Ensembl:ENSG00000151151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934986908 Functional Loss SNV dbSNP153 33..33 33 - - - 7608 RMVar_ID_7608 Human_SNP_ID_433962978 A-to-I Human chr10 + 58287007 58287007 58287007 AAGGCTGGAGTGCAGTGGCACAATCTCGGCTCACCGCAACTTCCCCTCCCAGGTTCAAGCCTCAG AAGGCTGGAGTGCAGTGGCACAATCTCGGCTCCCCGCAACTTCCCCTCCCAGGTTCAAGCCTCAG A C CISD1 Ensembl:ENSG00000122873 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1240312625 Functional Loss SNV dbSNP153 33..33 33 - - - 7609 RMVar_ID_7609 Human_SNP_ID_433962988 A-to-I Human chr10 + 58287060 58287060 58287060 TTCAAGCCTCAGCCTCCTGAGTAGCTGGGATTATGCGCACTCGCCACCATGCCTGGCTAATTTTT TTCAAGCCTCAGCCTCCTGAGTAGCTGGGATTCTGCGCACTCGCCACCATGCCTGGCTAATTTTT A C CISD1 Ensembl:ENSG00000122873 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs937255460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5980887 7610 RMVar_ID_7610 Human_SNP_ID_433963012 A-to-I Human chr10 + 58287173 58287173 58287173 GAACTCTTGACCTCAAATGATCCACCCACCTCAACCTCCCAAAGTGTTGAGATTACAGGCATGAG GAACTCTTGACCTCAAATGATCCACCCACCTCCACCTCCCAAAGTGTTGAGATTACAGGCATGAG A C CISD1 Ensembl:ENSG00000122873 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1300687719 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24817608 7611 RMVar_ID_7611 Human_SNP_ID_433988361 A-to-I Human chr10 + 58397890 58397890 58397890 GGCTCAAGTGATCCTTCCGAGTCGTTGGGACTACAGTAGGTGAACACCACCATGCCTGGCTAATT GGCTCAAGTGATCCTTCCGAGTCGTTGGGACTGCAGTAGGTGAACACCACCATGCCTGGCTAATT A G TFAM Ensembl:ENSG00000108064 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404356291 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_379221,Human_RBP_ID_1767928,Human_RBP_ID_5981548,Human_RBP_ID_8335894,Human_RBP_ID_11380265,Human_RBP_ID_17779207,Human_RBP_ID_18242261,Human_RBP_ID_23460906,Human_RBP_ID_27608791 RMVar_hsa_circ_266056 7612 RMVar_ID_7612 Human_SNP_ID_571906724 A-to-I Human chr15 - 30046058 30046058 30046058 TTTTTTTTTTTGAATGAGAAAACATTTATTCCATCTCCAAACAGCATCCCAGGGCCGGGCATCTC TTTTTTTTTTTGAATGAGAAAACATTTATTCCGTCTCCAAACAGCATCCCAGGGCCGGGCATCTC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs902820480 Functional Loss SNV dbSNP153 33..33 33 - - - 7613 RMVar_ID_7613 Human_SNP_ID_571982790 A-to-I Human chr15 + 30485056 30485056 30485056 AAGATCTTGGCTCACTACAACTTCCGCCTCCTAGGTTCAAGCAATTCTCGTGCCTTAGCCTGCCA AAGATCTTGGCTCACTACAACTTCCGCCTCCTGGGTTCAAGCAATTCTCGTGCCTTAGCCTGCCA A G AC127502.1 Ensembl:ENSG00000215302 Pseudogene intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1338285132 Functional Loss SNV dbSNP153 33..33 33 - - - 7614 RMVar_ID_7614 Human_SNP_ID_571982826 A-to-I Human chr15 + 30485163 30485163 30485163 TTTTGTATATTTTGTAGAGACGGGGTTTTGCCATGTTGGCTAGGCTGGTCTTGAACTCCCGACCT TTTTGTATATTTTGTAGAGACGGGGTTTTGCCGTGTTGGCTAGGCTGGTCTTGAACTCCCGACCT A G AC127502.1 Ensembl:ENSG00000215302 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1380709716 Functional Loss SNV dbSNP153 33..33 33 - - - 7615 RMVar_ID_7615 Human_SNP_ID_571983306 A-to-I Human chr15 + 30487125 30487123 30487125 CCCAGCACTTTGGGAGGCCGAGGCGGCAGATCACAGTGTCAGGAGATCGAGACCATCCTGGCTAA CCCAGCACTTTGGGAGGCCGAGGCGGCAGAT__CAGTGTCAGGAGATCGAGACCATCCTGGCTAA TCA T AC127502.1 Ensembl:ENSG00000215302 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1567436128 Functional Loss DEL dbSNP153 32..33 33 - - - 7616 RMVar_ID_7616 Human_SNP_ID_572011364 A-to-I Human chr15 - 30623253 30623253 30623253 TTTTGTAATTTTAGTAGAGACAGGGTTTCGCCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCT TTTTGTAATTTTAGTAGAGACAGGGTTTCGCCCTGTTGGCCAGGCTGGTCTCGAACTCCTGACCT T G AC091057.3 Ensembl:ENSG00000247728 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1303286595 Functional Loss SNV dbSNP153 33..33 33 - - - 7617 RMVar_ID_7617 Human_SNP_ID_572021786 A-to-I Human chr15 + 30662834 30662832 30662834 TTGGCCAGGCTGATCTGGAACTCTTGACCTCAAATAATCCACCCATCTCAGCCTCCCAAAGTGCT TTGGCCAGGCTGATCTGGAACTCTTGACCTC__ATAATCCACCCATCTCAGCCTCCCAAAGTGCT CAA C AC091057.6,ARHGAP11B,AC091057.1 Ensembl:ENSG00000285035,Ensembl:ENSG00000284906,Ensembl:ENSG00000187951 Pseudogene,Protein coding,lincRNA intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1452320693 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_25133098 RMVar_hsa_circ_170440,RMVar_hsa_circ_170439,RMVar_hsa_circ_371621,RMVar_hsa_circ_377077 7618 RMVar_ID_7618 Human_SNP_ID_572021882 A-to-I Human chr15 + 30663180 30663180 30663180 CTGGGAGGTTGAGGCTGCAGTGGGCTATTATCATGCTACTGCACTCCAGCTGGGTAACAGAGCAA CTGGGAGGTTGAGGCTGCAGTGGGCTATTATCGTGCTACTGCACTCCAGCTGGGTAACAGAGCAA A G AC091057.6,ARHGAP11B,AC091057.1 Ensembl:ENSG00000285035,Ensembl:ENSG00000284906,Ensembl:ENSG00000187951 Pseudogene,Protein coding,lincRNA intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978010159 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5246996 RMVar_hsa_circ_170440,RMVar_hsa_circ_170439,RMVar_hsa_circ_371621,RMVar_hsa_circ_377077 7619 RMVar_ID_7619 Human_SNP_ID_572051830 A-to-I Human chr15 + 30786377 30786377 30786377 TTAAAATTTTTTTGTAGCGATGGAGTCTCGTTATGTTGCCCGGACTGGTCTCGAACTCTTGGCCC TTAAAATTTTTTTGTAGCGATGGAGTCTCGTTGTGTTGCCCGGACTGGTCTCGAACTCTTGGCCC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1439065746 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8414813,Human_RBP_ID_12487291 7620 RMVar_ID_7620 Human_SNP_ID_572084071 A-to-I Human chr15 + 30907198 30907198 30907198 GAACTCTTGGTCCCAAGCGATCCTCCTGCCTCAGCCTCCCAAAGCACTGGGATTACAAGCATAAG GAACTCTTGGTCCCAAGCGATCCTCCTGCCTCGGCCTCCCAAAGCACTGGGATTACAAGCATAAG A G FAN1 Ensembl:ENSG00000198690 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1304065280 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_62386,RMVar_hsa_circ_115269,RMVar_hsa_circ_359455,RMVar_hsa_circ_170442,RMVar_hsa_circ_170443 7621 RMVar_ID_7621 Human_SNP_ID_572091723 A-to-I Human chr15 + 30934581 30934581 30934581 GTTTTTGTATTTTTTAGAGATGGGGTTCCACCATGTTGCCCAGGCTGATCTCAAATCCCCAGGCT GTTTTTGTATTTTTTAGAGATGGGGTTCCACCGTGTTGCCCAGGCTGATCTCAAATCCCCAGGCT A G FAN1 Ensembl:ENSG00000198690 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1050519716 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47541,RMVar_hsa_circ_86884,RMVar_hsa_circ_170449 7622 RMVar_ID_7622 Human_SNP_ID_572092570 A-to-I Human chr15 - 30937768 30937767 30937768 TAATGGTCAACAAAATTTTTCTCTTTTAAAAAAGTTCATTATGAGCTGGGTACAGTGGCTCAATG TAATGGTCAACAAAATTTTTCTCTTTTAAAAA_GTTCATTATGAGCTGGGTACAGTGGCTCAATG CT C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs887061111 Functional Loss DEL dbSNP153 33..33 33 - - - 7623 RMVar_ID_7623 Human_SNP_ID_572403502 A-to-I Human chr15 - 32169709 32169709 32169709 AAAGTTTCTCTTGTTTTAAGTTGCCCATCTCCAGTGAATCCACCCAAGGACTTTGAGCCAGCTTT AAAGTTTCTCTTGTTTTAAGTTGCCCATCTCCCGTGAATCCACCCAAGGACTTTGAGCCAGCTTT T G - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1366031544 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97189,RMVar_hsa_circ_101928,RMVar_hsa_circ_170469,RMVar_hsa_circ_170470 7624 RMVar_ID_7624 Human_SNP_ID_572455011 A-to-I Human chr15 - 32468275 32468275 32468275 TTGGACCGGAGGCGCGGTGGCTCACGCCTGCAATCCCAGCACCCAGGGAGGCGGAGGCGGGTGGA TTGGACCGGAGGCGCGGTGGCTCACGCCTGCACTCCCAGCACCCAGGGAGGCGGAGGCGGGTGGA T G - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1382172986 Functional Loss SNV dbSNP153 33..33 33 - - - 7625 RMVar_ID_7625 Human_SNP_ID_572463548 A-to-I Human chr15 - 32520522 32520522 32520522 CATTGTGAAACCTCGTCTCTACTAAAAATACAAAAAAATTAGCCGGGAGTGGTGGTGGGCGCCTG CATTGTGAAACCTCGTCTCTACTAAAAATACAGAAAAATTAGCCGGGAGTGGTGGTGGGCGCCTG T C AC135983.3 Ensembl:ENSG00000223509 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037283794 Functional Loss SNV dbSNP153 33..33 33 - - - 7626 RMVar_ID_7626 Human_SNP_ID_572463593 A-to-I Human chr15 - 32520630 32520628 32520653 ATTGTCTAAAATCCAGCCAGGCGCGGTGGTTCACGCCTGTACTCCCAGCACTTTGGGAGGCTGAG ATTGTCTAAGATCCAGCCAGGCGTGGTGGTTCACACCTGTACTCCCAGCACTTTGGGAGGCTGAG CGTGAACCACCGCGCCTGGCTGGATT TGTGAACCACCACGCCTGGCTGGATC AC135983.3 Ensembl:ENSG00000223509 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs71270746 Functional Loss MNV dbSNP153 10..35 33 - - - Human_RBP_ID_17563585,Human_RBP_ID_22523361 7627 RMVar_ID_7627 Human_SNP_ID_572464091 A-to-I Human chr15 - 32522552 32522552 32522552 TTTTGTATATTTTGTAGAGACGGGGTTTCGCCATGTTGGCTAGGCTGGTCTTGAACTCCCGACCT TTTTGTATATTTTGTAGAGACGGGGTTTCGCCGTGTTGGCTAGGCTGGTCTTGAACTCCCGACCT T C AC135983.3 Ensembl:ENSG00000223509 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1397736201 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17367190 7628 RMVar_ID_7628 Human_SNP_ID_572464127 A-to-I Human chr15 - 32522653 32522653 32522653 TTGGCTCACTACAACTTCCGCCTCCTAGGTTGAAGCAATTCTAGTGCCTTAGCCTGCCAAGTAGC TTGGCTCACTACAACTTCCGCCTCCTAGGTTGGAGCAATTCTAGTGCCTTAGCCTGCCAAGTAGC T C AC135983.3 Ensembl:ENSG00000223509 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1366487041 Functional Loss SNV dbSNP153 33..33 33 - - - 7629 RMVar_ID_7629 Human_SNP_ID_572464136 A-to-I Human chr15 - 32522675 32522675 32522675 GCTGGAGTGTGGAGGCAAGATCTTGGCTCACTACAACTTCCGCCTCCTAGGTTGAAGCAATTCTA GCTGGAGTGTGGAGGCAAGATCTTGGCTCACTGCAACTTCCGCCTCCTAGGTTGAAGCAATTCTA T C AC135983.3 Ensembl:ENSG00000223509 Pseudogene intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1435628461 Functional Loss SNV dbSNP153 33..33 33 - - - 7630 RMVar_ID_7630 Human_SNP_ID_572474766 A-to-I Human chr15 - 32580296 32580296 32580296 CCCGGTCCAATTTAGTAACCAGAAAGGAATAGATCTGCCTGGCGTGGTGCCTCCCCCTTGTGATC CCCGGTCCAATTTAGTAACCAGAAAGGAATAGGTCTGCCTGGCGTGGTGCCTCCCCCTTGTGATC T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1198734780 Functional Loss SNV dbSNP153 33..33 33 - - - 7631 RMVar_ID_7631 Human_SNP_ID_572481671 A-to-I Human chr15 - 32612647 32612647 32612647 TTTTGTAATTTTAGTAGAGACAGGGTTTCGCCATGTTGGCCAGGCTGGTCTCGAACTTCTGACCT TTTTGTAATTTTAGTAGAGACAGGGTTTCGCCCTGTTGGCCAGGCTGGTCTCGAACTTCTGACCT T G AC123768.3 Ensembl:ENSG00000262728 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1441091794 Functional Loss SNV dbSNP153 33..33 33 - - - 7632 RMVar_ID_7632 Human_SNP_ID_572484298 A-to-I Human chr15 + 32621670 32621670 32621670 ACACAGTGAAACCCCGTCTCTACTAAAAATACAAAACATTAGCTGAGTGTGGTAGCACGCACCTG ACACAGTGAAACCCCGTCTCTACTAAAAATACGAAACATTAGCTGAGTGTGGTAGCACGCACCTG A G ARHGAP11A Ensembl:ENSG00000198826 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs528787851 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4331,RMVar_hsa_circ_101200,RMVar_hsa_circ_105871,RMVar_hsa_circ_170474,RMVar_hsa_circ_66213,RMVar_hsa_circ_170475 7633 RMVar_ID_7633 Human_SNP_ID_572484309 A-to-I Human chr15 + 32621704 32621704 32621704 AACATTAGCTGAGTGTGGTAGCACGCACCTGTAGTTCCAGCTACTCGGGAGGCTGAGGCAGGGGA AACATTAGCTGAGTGTGGTAGCACGCACCTGTCGTTCCAGCTACTCGGGAGGCTGAGGCAGGGGA A C ARHGAP11A Ensembl:ENSG00000198826 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1222986080 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4331,RMVar_hsa_circ_101200,RMVar_hsa_circ_105871,RMVar_hsa_circ_170474,RMVar_hsa_circ_66213,RMVar_hsa_circ_170475 7634 RMVar_ID_7634 Human_SNP_ID_572488682 A-to-I Human chr15 + 32638178 32638178 32638178 TCACTGCAAGCTCCACTTCCTGGGTTCATGCCATTTTCCTGCCTCAGCCTCCCGAGTAGCTGGGA TCACTGCAAGCTCCACTTCCTGGGTTCATGCCGTTTTCCTGCCTCAGCCTCCCGAGTAGCTGGGA A G ARHGAP11A Ensembl:ENSG00000198826 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1434438584 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_420346,Human_miRNA_ID_1657451 7635 RMVar_ID_7635 Human_SNP_ID_572488753 A-to-I Human chr15 + 32638351 32638351 32638351 CCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCACGCCCGGCTAGACTTTACCTTT CCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCACGCCCGGCTAGACTTTACCTTT A G ARHGAP11A Ensembl:ENSG00000198826 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs996219123 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1697538 7636 RMVar_ID_7636 Human_SNP_ID_572489823 A-to-I Human chr15 + 32642447 32642447 32642447 AAAATTAGCCGGGTTTGGTTGTGGGCGCCTGTAATTCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTAGCCGGGTTTGGTTGTGGGCGCCTGTGATTCCAGCTACTCGGGAGGCTGAGGCAGGAGA A G SCG5 Ensembl:ENSG00000166922 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1019625016 Functional Loss SNV dbSNP153 33..33 33 - - - 7637 RMVar_ID_7637 Human_SNP_ID_572491809 A-to-I Human chr15 + 32650927 32650927 32650927 AACATTAAAATACCCACGTTCTGCCGGGCGCGATGGCTCACGCCTGTAATCCCAGCACTTTGGGA AACATTAAAATACCCACGTTCTGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGA A G SCG5 Ensembl:ENSG00000166922 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1323843145 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6417698 RMVar_hsa_circ_376146,RMVar_hsa_circ_96230,RMVar_hsa_circ_170478,RMVar_hsa_circ_170479 7638 RMVar_ID_7638 Human_SNP_ID_572556377 A-to-I Human chr15 - 32891380 32891380 32891380 AGCTGGGCGTGGTGGCGGGTGCCTGTGGTCCCAGCTGCTTGGGAGGCTGAGGCAGGAGAATGGCG AGCTGGGCGTGGTGGCGGGTGCCTGTGGTCCCGGCTGCTTGGGAGGCTGAGGCAGGAGAATGGCG T C FMN1 Ensembl:ENSG00000248905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs896465325 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_170485,RMVar_hsa_circ_320482,RMVar_hsa_circ_377884,RMVar_hsa_circ_170486,RMVar_hsa_circ_170488,RMVar_hsa_circ_295968,RMVar_hsa_circ_340071,RMVar_hsa_circ_170487 7639 RMVar_ID_7639 Human_SNP_ID_572643500 A-to-I Human chr15 - 33161760 33161760 33161760 GTGCTCGCCACCACACCTGGCTAATATTTTGTATTTTTAGTGGAGACGGGGTTTCACCGTGTTGG GTGCTCGCCACCACACCTGGCTAATATTTTGTGTTTTTAGTGGAGACGGGGTTTCACCGTGTTGG T C FMN1 Ensembl:ENSG00000248905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs765558307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12489108 7640 RMVar_ID_7640 Human_SNP_ID_572821180 A-to-I Human chr15 + 33850217 33850217 33850217 CCTGGCCAACATAGTGAAACCCCGTCTCTACTAAAAATACAAAAAAATTAGCTGAGCGTGGTGGT CCTGGCCAACATAGTGAAACCCCGTCTCTACTGAAAATACAAAAAAATTAGCTGAGCGTGGTGGT A G RYR3 Ensembl:ENSG00000198838 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1305555772 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_332939,RMVar_hsa_circ_50174,RMVar_hsa_circ_40019 7641 RMVar_ID_7641 Human_SNP_ID_572827750 A-to-I Human chr15 - 33866700 33866700 33866700 CCAGTTTGTGCAAAACCATCTGTGACTGAAGAAAAAAACATGGAACCTGAGCAACCAAGTACCTC CCAGTTTGTGCAAAACCATCTGTGACTGAAGAGAAAAACATGGAACCTGAGCAACCAAGTACCTC T C AVEN Ensembl:ENSG00000169857 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1378711313 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18981320 Human_Splice_Rec_1579750,Human_Splice_Rec_1579756 RMVar_hsa_circ_77315,RMVar_hsa_circ_100574,RMVar_hsa_circ_170515,RMVar_hsa_circ_170516 7642 RMVar_ID_7642 Human_SNP_ID_572849687 A-to-I Human chr15 - 33945786 33945786 33945786 GGTCAGGAGATCGAGACTATCCTGGCCAACATAGCGAAACCCCGTCTCTACGAAAATACAAAAAA GGTCAGGAGATCGAGACTATCCTGGCCAACATGGCGAAACCCCGTCTCTACGAAAATACAAAAAA T C AVEN Ensembl:ENSG00000169857 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs551527369 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_170517,RMVar_hsa_circ_100574,RMVar_hsa_circ_170516,RMVar_hsa_circ_84374 7643 RMVar_ID_7643 Human_SNP_ID_572884535 A-to-I Human chr15 - 34087934 34087934 34087934 TTTGAGTGGCCTCAAACTCCTGGGCTCAAGCTATCCACCTGCCTCAGCCTCCCAAAGCACTGGGA TTTGAGTGGCCTCAAACTCCTGGGCTCAAGCTGTCCACCTGCCTCAGCCTCCCAAAGCACTGGGA T C EMC7 Ensembl:ENSG00000134153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1393383854 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_170521,RMVar_hsa_circ_170522,RMVar_hsa_circ_170520 7644 RMVar_ID_7644 Human_SNP_ID_572886953 A-to-I Human chr15 - 34097131 34097129 34097131 TACTCGGGAGACTGAGGAAGGAGAATGGCGTGAACGCAGGAGGCGGAGCTTGCAGTGAGCCGAGA TACTCGGGAGACTGAGGAAGGAGAATGGCGTG__CGCAGGAGGCGGAGCTTGCAGTGAGCCGAGA GTT G EMC7 Ensembl:ENSG00000134153 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1203620928 Functional Loss DEL dbSNP153 33..34 33 - - - 7645 RMVar_ID_7645 Human_SNP_ID_572886965 A-to-I Human chr15 - 34097172 34097172 34097172 AAAATTAACCGGGCGTGATGGAGGGCGCCTGTAGTCCCAGCTACTCGGGAGACTGAGGAAGGAGA AAAATTAACCGGGCGTGATGGAGGGCGCCTGTGGTCCCAGCTACTCGGGAGACTGAGGAAGGAGA T C EMC7 Ensembl:ENSG00000134153 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs965950367 Functional Loss SNV dbSNP153 33..33 33 - - - 7646 RMVar_ID_7646 Human_SNP_ID_572887088 A-to-I Human chr15 - 34097784 34097784 34097784 TTGTATTTTTAGTAGAGACAGGGTTTCACCGTATTAGTCAGGATGGTCTCGTCATCTTGCTTTTT TTGTATTTTTAGTAGAGACAGGGTTTCACCGTGTTAGTCAGGATGGTCTCGTCATCTTGCTTTTT T C EMC7 Ensembl:ENSG00000134153 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1366641038 Functional Loss SNV dbSNP153 33..33 33 - - - 7647 RMVar_ID_7647 Human_SNP_ID_572887115 A-to-I Human chr15 - 34097887 34097887 34097887 TCGGCTCATTGCAACTTCCGCCTCCCAGGTTCAAGTGATTCTCCTGCCCCAGCCTCCTGAGTAGC TCGGCTCATTGCAACTTCCGCCTCCCAGGTTCGAGTGATTCTCCTGCCCCAGCCTCCTGAGTAGC T C EMC7 Ensembl:ENSG00000134153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1390265374 Functional Loss SNV dbSNP153 33..33 33 - - - 7648 RMVar_ID_7648 Human_SNP_ID_572887578 A-to-I Human chr15 - 34099773 34099773 34099773 TAGTGGGACCCCATTTCTACAAAAAATAAATAATTAGCCAGGAGTGGTGGTGTGCACCTGTAGTC TAGTGGGACCCCATTTCTACAAAAAATAAATACTTAGCCAGGAGTGGTGGTGTGCACCTGTAGTC T G EMC7 Ensembl:ENSG00000134153 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs977255486 Functional Loss SNV dbSNP153 33..33 33 - - - 7649 RMVar_ID_7649 Human_SNP_ID_572887579 A-to-I Human chr15 - 34099787 34099787 34099787 CAGCTGGGGCAACATAGTGGGACCCCATTTCTACAAAAAATAAATAATTAGCCAGGAGTGGTGGT CAGCTGGGGCAACATAGTGGGACCCCATTTCTGCAAAAAATAAATAATTAGCCAGGAGTGGTGGT T C EMC7 Ensembl:ENSG00000134153 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1208433168 Functional Loss SNV dbSNP153 33..33 33 - - - 7650 RMVar_ID_7650 Human_SNP_ID_572887672 A-to-I Human chr15 - 34100209 34100209 34100209 AGCCTCCTCAGTAGATAGGACTACAGGCGGACACCATCATGTCCAGCTAATTTTTTAATTTTTTG AGCCTCCTCAGTAGATAGGACTACAGGCGGACTCCATCATGTCCAGCTAATTTTTTAATTTTTTG T A EMC7 Ensembl:ENSG00000134153 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2705351 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_621,GWAS_ID_622,GWAS_ID_623 7651 RMVar_ID_7651 Human_SNP_ID_572887673 A-to-I Human chr15 - 34100209 34100209 34100209 AGCCTCCTCAGTAGATAGGACTACAGGCGGACACCATCATGTCCAGCTAATTTTTTAATTTTTTG AGCCTCCTCAGTAGATAGGACTACAGGCGGACGCCATCATGTCCAGCTAATTTTTTAATTTTTTG T C EMC7 Ensembl:ENSG00000134153 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2705351 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_621,GWAS_ID_622,GWAS_ID_623 7652 RMVar_ID_7652 Human_SNP_ID_572887679 A-to-I Human chr15 - 34100229 34100229 34100229 TCAAGTGATCCTCCTGTCTCAGCCTCCTCAGTAGATAGGACTACAGGCGGACACCATCATGTCCA TCAAGTGATCCTCCTGTCTCAGCCTCCTCAGTGGATAGGACTACAGGCGGACACCATCATGTCCA T C EMC7 Ensembl:ENSG00000134153 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs899434875 Functional Loss SNV dbSNP153 33..33 33 - - - 7653 RMVar_ID_7653 Human_SNP_ID_572889298 A-to-I Human chr15 + 34106244 34106244 34106244 CACAAGGTCAGGAGTTTGAGACTAGCCTGGCCAACATGGTGAAACCCTGTCTCTACTAAAAATAC CACAAGGTCAGGAGTTTGAGACTAGCCTGGCCGACATGGTGAAACCCTGTCTCTACTAAAAATAC A G PGBD4 Ensembl:ENSG00000182405 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs147954291 Functional Loss SNV dbSNP153 33..33 33 - - - 7654 RMVar_ID_7654 Human_SNP_ID_572896701 A-to-I Human chr15 - 34136861 34136860 34136861 ACCACGCCCGGGTAATTTTTTTGTATTTTTTTAGTAGAGACGGGGTTTCACCGTGTTAGGCAGGA ACCACGCCCGGGTAATTTTTTTGTATTTTTTT_GTAGAGACGGGGTTTCACCGTGTTAGGCAGGA CT C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1186987109 Functional Loss DEL dbSNP153 33..33 33 - - - 7655 RMVar_ID_7655 Human_SNP_ID_572896702 A-to-I Human chr15 - 34136861 34136861 34136861 ACCACGCCCGGGTAATTTTTTTGTATTTTTTTAGTAGAGACGGGGTTTCACCGTGTTAGGCAGGA ACCACGCCCGGGTAATTTTTTTGTATTTTTTTGGTAGAGACGGGGTTTCACCGTGTTAGGCAGGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1443010386 Functional Loss SNV dbSNP153 33..33 33 - - - 7656 RMVar_ID_7656 Human_SNP_ID_572898253 A-to-I Human chr15 - 34142900 34142900 34142900 CGAGACCATCCCGGCCAACATGGTGAAACCCCATCTCTACTAAAACACAAAAAATTAGCCGGGCG CGAGACCATCCCGGCCAACATGGTGAAACCCCGTCTCTACTAAAACACAAAAAATTAGCCGGGCG T C KATNBL1 Ensembl:ENSG00000134152 Protein coding intron GSE47997;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,32596459 RNA-Seq:(High) rs763927160 Functional Loss SNV dbSNP153 33..33 33 - - - 7657 RMVar_ID_7657 Human_SNP_ID_572898259 A-to-I Human chr15 - 34142913 34142913 34142913 GAGCTCAGGAGATCGAGACCATCCCGGCCAACATGGTGAAACCCCATCTCTACTAAAACACAAAA GAGCTCAGGAGATCGAGACCATCCCGGCCAACGTGGTGAAACCCCATCTCTACTAAAACACAAAA T C KATNBL1 Ensembl:ENSG00000134152 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1289418243 Functional Loss SNV dbSNP153 33..33 33 - - - 7658 RMVar_ID_7658 Human_SNP_ID_572898260 A-to-I Human chr15 - 34142915 34142915 34142915 ACGAGCTCAGGAGATCGAGACCATCCCGGCCAACATGGTGAAACCCCATCTCTACTAAAACACAA ACGAGCTCAGGAGATCGAGACCATCCCGGCCAGCATGGTGAAACCCCATCTCTACTAAAACACAA T C KATNBL1 Ensembl:ENSG00000134152 Protein coding intron GSE47997;GSE38233;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,32596459 RNA-Seq:(High) rs970007164 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25133704 7659 RMVar_ID_7659 Human_SNP_ID_572898274 A-to-I Human chr15 - 34142939 34142939 34142939 TTGGGAGGCCAAGGTGGGCAGATCACGAGCTCAGGAGATCGAGACCATCCCGGCCAACATGGTGA TTGGGAGGCCAAGGTGGGCAGATCACGAGCTCGGGAGATCGAGACCATCCCGGCCAACATGGTGA T C KATNBL1 Ensembl:ENSG00000134152 Protein coding intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1327923300 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1579832 7660 RMVar_ID_7660 Human_SNP_ID_572898383 A-to-I Human chr15 - 34143257 34143257 34143257 TTGGCCAGGCTGGTTTCGAACTCCTGACCTCAAGTGACCCACCCACCTCCCCCTCCCAAAGTAAT TTGGCCAGGCTGGTTTCGAACTCCTGACCTCAGGTGACCCACCCACCTCCCCCTCCCAAAGTAAT T C KATNBL1 Ensembl:ENSG00000134152 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1357824651 Functional Loss SNV dbSNP153 33..33 33 - - - 7661 RMVar_ID_7661 Human_SNP_ID_572898394 A-to-I Human chr15 - 34143318 34143318 34143318 TGGGATTACACACATGCCTGGCTAATTTTTGTATTTTTAGTGGAGACGGGATTTCACCACGTTGG TGGGATTACACACATGCCTGGCTAATTTTTGTGTTTTTAGTGGAGACGGGATTTCACCACGTTGG T C KATNBL1 Ensembl:ENSG00000134152 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1189747392 Functional Loss SNV dbSNP153 33..33 33 - - - 7662 RMVar_ID_7662 Human_SNP_ID_572898396 A-to-I Human chr15 - 34143327 34143327 34143327 CCGAGTAGCTGGGATTACACACATGCCTGGCTAATTTTTGTATTTTTAGTGGAGACGGGATTTCA CCGAGTAGCTGGGATTACACACATGCCTGGCTGATTTTTGTATTTTTAGTGGAGACGGGATTTCA T C KATNBL1 Ensembl:ENSG00000134152 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971791193 Functional Loss SNV dbSNP153 33..33 33 - - - 7663 RMVar_ID_7663 Human_SNP_ID_572898407 A-to-I Human chr15 - 34143378 34143378 34143378 TCACTGCAACCTCTGCCTCCTGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGA TCACTGCAACCTCTGCCTCCTGGGTTCAAGTGGTTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGA T C KATNBL1 Ensembl:ENSG00000134152 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs113704568 Functional Loss SNV dbSNP153 33..33 33 - - - 7664 RMVar_ID_7664 Human_SNP_ID_572898408 A-to-I Human chr15 - 34143378 34143378 34143378 TCACTGCAACCTCTGCCTCCTGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGA TCACTGCAACCTCTGCCTCCTGGGTTCAAGTGCTTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGA T G KATNBL1 Ensembl:ENSG00000134152 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs113704568 Functional Loss SNV dbSNP153 33..33 33 - - - 7665 RMVar_ID_7665 Human_SNP_ID_572898419 A-to-I Human chr15 - 34143419 34143419 34143419 GCTCTGTCGTCCAGGCTGGAGTGCAGTGGCACAAGCTCAGCTCACTGCAACCTCTGCCTCCTGGG GCTCTGTCGTCCAGGCTGGAGTGCAGTGGCACGAGCTCAGCTCACTGCAACCTCTGCCTCCTGGG T C KATNBL1 Ensembl:ENSG00000134152 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1369858986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12489561,Human_RBP_ID_25184862 7666 RMVar_ID_7666 Human_SNP_ID_572898434 A-to-I Human chr15 - 34143456 34143456 34143456 AATTTTTTTTGTTGTTTTTGTTTTGAGACTGAATCTCGCTCTGTCGTCCAGGCTGGAGTGCAGTG AATTTTTTTTGTTGTTTTTGTTTTGAGACTGAGTCTCGCTCTGTCGTCCAGGCTGGAGTGCAGTG T C KATNBL1 Ensembl:ENSG00000134152 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs186750831 Functional Loss SNV dbSNP153 33..33 33 - - - 7667 RMVar_ID_7667 Human_SNP_ID_572898561 A-to-I Human chr15 - 34143880 34143880 34143880 TCACTACAAGCTCCACCTCCCAGGTTCACGCCATTCTCCTGCCTCAGCCTCCCGATTAGCTGGGA TCACTACAAGCTCCACCTCCCAGGTTCACGCCGTTCTCCTGCCTCAGCCTCCCGATTAGCTGGGA T C KATNBL1 Ensembl:ENSG00000134152 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1321774051 Functional Loss SNV dbSNP153 33..33 33 - - - 7668 RMVar_ID_7668 Human_SNP_ID_572898573 A-to-I Human chr15 - 34143920 34143920 34143920 CTCTGTCGCCCAGGCTGGAGTGTGGTGGCGCAATCTCGGCTCACTACAAGCTCCACCTCCCAGGT CTCTGTCGCCCAGGCTGGAGTGTGGTGGCGCAGTCTCGGCTCACTACAAGCTCCACCTCCCAGGT T C KATNBL1 Ensembl:ENSG00000134152 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs551559771 Functional Loss SNV dbSNP153 33..33 33 - - - 7669 RMVar_ID_7669 Human_SNP_ID_572898808 A-to-I Human chr15 - 34144794 34144794 34144794 GGGAGGCCAAGGCAAGCAGATCACCTGAGGTCAGGAGTTCGAGACCAGCCTGGTTGGTGAAACCC GGGAGGCCAAGGCAAGCAGATCACCTGAGGTCTGGAGTTCGAGACCAGCCTGGTTGGTGAAACCC T A KATNBL1 Ensembl:ENSG00000134152 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1173136584 Functional Loss SNV dbSNP153 33..33 33 - - - 7670 RMVar_ID_7670 Human_SNP_ID_572898812 A-to-I Human chr15 - 34144809 34144809 34144809 TAATCCTAGCACTTAGGGAGGCCAAGGCAAGCAGATCACCTGAGGTCAGGAGTTCGAGACCAGCC TAATCCTAGCACTTAGGGAGGCCAAGGCAAGCGGATCACCTGAGGTCAGGAGTTCGAGACCAGCC T C KATNBL1 Ensembl:ENSG00000134152 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1420292954 Functional Loss SNV dbSNP153 33..33 33 - - - 7671 RMVar_ID_7671 Human_SNP_ID_572898813 A-to-I Human chr15 - 34144809 34144809 34144809 TAATCCTAGCACTTAGGGAGGCCAAGGCAAGCAGATCACCTGAGGTCAGGAGTTCGAGACCAGCC TAATCCTAGCACTTAGGGAGGCCAAGGCAAGCCGATCACCTGAGGTCAGGAGTTCGAGACCAGCC T G KATNBL1 Ensembl:ENSG00000134152 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1420292954 Functional Loss SNV dbSNP153 33..33 33 - - - 7672 RMVar_ID_7672 Human_SNP_ID_572898816 A-to-I Human chr15 - 34144839 34144839 34144839 AGTTAGGCCGGGCACAGTGGCTTACGCCTGTAATCCTAGCACTTAGGGAGGCCAAGGCAAGCAGA AGTTAGGCCGGGCACAGTGGCTTACGCCTGTATTCCTAGCACTTAGGGAGGCCAAGGCAAGCAGA T A KATNBL1 Ensembl:ENSG00000134152 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1214025628 Functional Loss SNV dbSNP153 33..33 33 - - - 7673 RMVar_ID_7673 Human_SNP_ID_572899544 A-to-I Human chr15 - 34147943 34147943 34147943 AGATCACTTTGAACCCAGGAGTTGGAGGTTGCAGTAAGCTGTGATTATGCAACTACATTCCAGCC AGATCACTTTGAACCCAGGAGTTGGAGGTTGCCGTAAGCTGTGATTATGCAACTACATTCCAGCC T G KATNBL1 Ensembl:ENSG00000134152 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1293755892 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17563167 RMVar_hsa_circ_40464,RMVar_hsa_circ_324450,RMVar_hsa_circ_337094,RMVar_hsa_circ_349532,RMVar_hsa_circ_315947,RMVar_hsa_circ_378795 7674 RMVar_ID_7674 Human_SNP_ID_572908802 A-to-I Human chr15 - 34183911 34183911 34183911 ACCTGCCTCGGCCTCCCAGAGTGCTGAAATTAAGGCATGAGCCACCGCACCCAGCCGAGTTTAGG ACCTGCCTCGGCCTCCCAGAGTGCTGAAATTACGGCATGAGCCACCGCACCCAGCCGAGTTTAGG T G KATNBL1 Ensembl:ENSG00000134152 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1424962557 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_340802 7675 RMVar_ID_7675 Human_SNP_ID_572920969 A-to-I Human chr15 + 34230010 34230010 34230010 TATACCATAACCCAAGGCTGAAAATAATGTAGAAAACTTTATTTTTGTTTCCAGTACAGAGCAAA TATACCATAACCCAAGGCTGAAAATAATGTAGCAAACTTTATTTTTGTTTCCAGTACAGAGCAAA A C EMC4 Ensembl:ENSG00000128463 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1278114040 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1828457,Human_RBP_ID_5141360,Human_RBP_ID_6418331,Human_RBP_ID_17858841,Human_RBP_ID_21887980,Human_RBP_ID_22387801,Human_RBP_ID_23208823,Human_RBP_ID_23648541 7676 RMVar_ID_7676 Human_SNP_ID_572920997 A-to-I Human chr15 - 34230084 34230082 34230085 GGAGATGCTGCAACAGTTCTTGATTTAGCAGCAGTTATTCTCTTGTTTACATAGTTATGTTTTTT GGAGATGCTGCAACAGTTCTTGATTTAGCAG___TTATTCTCTTGTTTACATAGTTATGTTTTTT ACTG A SLC12A6 Ensembl:ENSG00000140199 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1327169987 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_6418334,Human_RBP_ID_8947390 7677 RMVar_ID_7677 Human_SNP_ID_572920998 A-to-I Human chr15 - 34230084 34230084 34230084 GGAGATGCTGCAACAGTTCTTGATTTAGCAGCAGTTATTCTCTTGTTTACATAGTTATGTTTTTT GGAGATGCTGCAACAGTTCTTGATTTAGCAGCGGTTATTCTCTTGTTTACATAGTTATGTTTTTT T C SLC12A6 Ensembl:ENSG00000140199 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1255661906 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6418334,Human_RBP_ID_8947390 7678 RMVar_ID_7678 Human_SNP_ID_572921269 A-to-I Human chr15 - 34231108 34231108 34231108 CCTCAGGTGATCCGCCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGTGCC CCTCAGGTGATCCGCCCGCCTTGGCCTCCCAAGGTGCTGGGATTACAGGCGTGAGCCACTGTGCC T C SLC12A6 Ensembl:ENSG00000140199 Protein coding 3'UTR GSE47997;GSE38233;GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;cultured B-cells;cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,24183664,24183664,31158229,31158229,31158229 RNA-Seq:(High) rs958752052 Functional Loss SNV dbSNP153 33..33 33 - - - 7679 RMVar_ID_7679 Human_SNP_ID_572921270 A-to-I Human chr15 - 34231110 34231110 34231110 AACCTCAGGTGATCCGCCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGTG AACCTCAGGTGATCCGCCCGCCTTGGCCTCCCCAAGTGCTGGGATTACAGGCGTGAGCCACTGTG T G SLC12A6 Ensembl:ENSG00000140199 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs990618951 Functional Loss SNV dbSNP153 33..33 33 - - - 7680 RMVar_ID_7680 Human_SNP_ID_572921297 A-to-I Human chr15 - 34231206 34231195 34231207 AAGCATGTGCCACCACACCCAGCTAATTTTGTATTTTCAGTAGAGACGGGGTTTCTCTACTGAAA AAGCATGTGCCACCACACCCAGCTAATTTTG____________AGACGGGGTTTCTCTACTGAAA TCTACTGAAAATA T SLC12A6 Ensembl:ENSG00000140199 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1267464808 Functional Loss DEL dbSNP153 32..43 33 - - - 7681 RMVar_ID_7681 Human_SNP_ID_572921298 A-to-I Human chr15 - 34231197 34231197 34231197 CCACCACACCCAGCTAATTTTGTATTTTCAGTAGAGACGGGGTTTCTCTACTGAAACTGATGTTG CCACCACACCCAGCTAATTTTGTATTTTCAGTGGAGACGGGGTTTCTCTACTGAAACTGATGTTG T C SLC12A6 Ensembl:ENSG00000140199 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs886051040 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_40 7682 RMVar_ID_7682 Human_SNP_ID_572921315 A-to-I Human chr15 - 34231262 34231262 34231262 TGCCTCCTGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGAATTACAAGCATGTG TGCCTCCTGGGTTCAAGCGATTCTCCTGCCTCGGCCTCCCGAGTAGCTGGAATTACAAGCATGTG T C SLC12A6 Ensembl:ENSG00000140199 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs890860839 Functional Loss SNV dbSNP153 33..33 33 - - - 7683 RMVar_ID_7683 Human_SNP_ID_572921319 A-to-I Human chr15 - 34231275 34231275 34231275 TCACCGCAACCTCTGCCTCCTGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGAA TCACCGCAACCTCTGCCTCCTGGGTTCAAGCGGTTCTCCTGCCTCAGCCTCCCGAGTAGCTGGAA T C SLC12A6 Ensembl:ENSG00000140199 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1312475529 Functional Loss SNV dbSNP153 33..33 33 - - - 7684 RMVar_ID_7684 Human_SNP_ID_572921322 A-to-I Human chr15 - 34231279 34231278 34231280 TGGCTCACCGCAACCTCTGCCTCCTGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCT TGGCTCACCGCAACCTCTGCCTCCTGGGTTC__GCGATTCTCCTGCCTCAGCCTCCCGAGTAGCT CTT C SLC12A6 Ensembl:ENSG00000140199 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1341271748 Functional Loss DEL dbSNP153 32..33 33 - - - 7685 RMVar_ID_7685 Human_SNP_ID_572921322 A-to-I Human chr15 - 34231280 34231278 34231280 TTGGCTCACCGCAACCTCTGCCTCCTGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGC TTGGCTCACCGCAACCTCTGCCTCCTGGGTTC__GCGATTCTCCTGCCTCAGCCTCCCGAGTAGC CTT C SLC12A6 Ensembl:ENSG00000140199 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1341271748 Functional Loss DEL dbSNP153 33..34 33 - - - 7686 RMVar_ID_7686 Human_SNP_ID_572921464 A-to-I Human chr15 - 34231650 34231650 34231650 GGGAGGTGGAACTTGCAGTGAACCGAGATTGCACCACTGCACTCCAGCCTGGGCGACAGAGGGAG GGGAGGTGGAACTTGCAGTGAACCGAGATTGCGCCACTGCACTCCAGCCTGGGCGACAGAGGGAG T C SLC12A6 Ensembl:ENSG00000140199 Protein coding 3'UTR GSE38233;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;ASD brains,temporal_cortex;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,30559470,31158229,31158229,31158229 RNA-Seq:(High) rs923093610 Functional Loss SNV dbSNP153 33..33 33 - - - 7687 RMVar_ID_7687 Human_SNP_ID_572921465 A-to-I Human chr15 - 34231650 34231650 34231650 GGGAGGTGGAACTTGCAGTGAACCGAGATTGCACCACTGCACTCCAGCCTGGGCGACAGAGGGAG GGGAGGTGGAACTTGCAGTGAACCGAGATTGCCCCACTGCACTCCAGCCTGGGCGACAGAGGGAG T G SLC12A6 Ensembl:ENSG00000140199 Protein coding 3'UTR GSE38233;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;ASD brains,temporal_cortex;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,30559470,31158229,31158229,31158229 RNA-Seq:(High) rs923093610 Functional Loss SNV dbSNP153 33..33 33 - - - 7688 RMVar_ID_7688 Human_SNP_ID_572921472 A-to-I Human chr15 - 34231661 34231661 34231661 GGCGTGAACCCGGGAGGTGGAACTTGCAGTGAACCGAGATTGCACCACTGCACTCCAGCCTGGGC GGCGTGAACCCGGGAGGTGGAACTTGCAGTGAGCCGAGATTGCACCACTGCACTCCAGCCTGGGC T C SLC12A6 Ensembl:ENSG00000140199 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs886051042 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_41 7689 RMVar_ID_7689 Human_SNP_ID_572921475 A-to-I Human chr15 - 34231666 34231666 34231666 AGAATGGCGTGAACCCGGGAGGTGGAACTTGCAGTGAACCGAGATTGCACCACTGCACTCCAGCC AGAATGGCGTGAACCCGGGAGGTGGAACTTGCGGTGAACCGAGATTGCACCACTGCACTCCAGCC T C SLC12A6 Ensembl:ENSG00000140199 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1250080683 Functional Loss SNV dbSNP153 33..33 33 - - - 7690 RMVar_ID_7690 Human_SNP_ID_572921476 A-to-I Human chr15 - 34231666 34231666 34231666 AGAATGGCGTGAACCCGGGAGGTGGAACTTGCAGTGAACCGAGATTGCACCACTGCACTCCAGCC AGAATGGCGTGAACCCGGGAGGTGGAACTTGCCGTGAACCGAGATTGCACCACTGCACTCCAGCC T G SLC12A6 Ensembl:ENSG00000140199 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1250080683 Functional Loss SNV dbSNP153 33..33 33 - - - 7691 RMVar_ID_7691 Human_SNP_ID_572921515 A-to-I Human chr15 - 34231754 34231754 34231754 AAACCCTGTCTCTACAAAAATACAAAAAAATTAGTCGGGCATGGTGGCGGGCGCCTGTAGTCCCA AAACCCTGTCTCTACAAAAATACAAAAAAATTCGTCGGGCATGGTGGCGGGCGCCTGTAGTCCCA T G SLC12A6 Ensembl:ENSG00000140199 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs931619573 Functional Loss SNV dbSNP153 33..33 33 - - - 7692 RMVar_ID_7692 Human_SNP_ID_572921546 A-to-I Human chr15 - 34231836 34231836 34231836 CCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGCGGATCACGAGGTCAGGAGATTTGAGACCA CCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGGATCACGAGGTCAGGAGATTTGAGACCA T C SLC12A6 Ensembl:ENSG00000140199 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1046116385 Functional Loss SNV dbSNP153 33..33 33 - - - 7693 RMVar_ID_7693 Human_SNP_ID_572921665 A-to-I Human chr15 - 34232304 34232304 34232304 AGGATCATTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCCAGGATTGCACCTCTGCACTCCAGCC AGGATCATTTGAACCCAGGAGGCGGAGGTTGCGGTGAGCCAGGATTGCACCTCTGCACTCCAGCC T C SLC12A6 Ensembl:ENSG00000140199 Protein coding 3'UTR GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1443227935 Functional Loss SNV dbSNP153 33..33 33 - - - 7694 RMVar_ID_7694 Human_SNP_ID_572921685 A-to-I Human chr15 - 34232384 34232384 34232384 GTCTATACTAAAAATACAAAAATTAGCTGGGCATGGTGGTGCATGCCTGTGATCCCAGCAACACG GTCTATACTAAAAATACAAAAATTAGCTGGGCGTGGTGGTGCATGCCTGTGATCCCAGCAACACG T C SLC12A6 Ensembl:ENSG00000140199 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1038446005 Functional Loss SNV dbSNP153 33..33 33 - - - 7695 RMVar_ID_7695 Human_SNP_ID_572921692 A-to-I Human chr15 - 34232407 34232407 34232407 CCTGGCCAACATGGTGAAAACCTGTCTATACTAAAAATACAAAAATTAGCTGGGCATGGTGGTGC CCTGGCCAACATGGTGAAAACCTGTCTATACTGAAAATACAAAAATTAGCTGGGCATGGTGGTGC T C SLC12A6 Ensembl:ENSG00000140199 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831 Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line - 31158229,32596459 RNA-Seq:(High) rs571583480 Functional Loss SNV dbSNP153 33..33 33 - - - 7696 RMVar_ID_7696 Human_SNP_ID_572925349 A-to-I Human chr15 - 34247807 34247807 34247807 CTAGCTACTGGGAAGGCTGAGGCAGAAAGATCACTTGAACCCAGGAGGTTGAGGCTACAGTCAGT CTAGCTACTGGGAAGGCTGAGGCAGAAAGATCCCTTGAACCCAGGAGGTTGAGGCTACAGTCAGT T G SLC12A6 Ensembl:ENSG00000140199 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs12902276 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57278,RMVar_hsa_circ_282622,RMVar_hsa_circ_4247,RMVar_hsa_circ_349344,RMVar_hsa_circ_348561,RMVar_hsa_circ_311141,RMVar_hsa_circ_170534,RMVar_hsa_circ_170535,RMVar_hsa_circ_96154 7697 RMVar_ID_7697 Human_SNP_ID_572930762 A-to-I Human chr15 - 34270386 34270386 34270386 ATAATGATAATTTAAAAAATGAGCCAGGCACAATGGCACACGCCTGTAGTCCCAGCACTTTAGGA ATAATGATAATTTAAAAAATGAGCCAGGCACAGTGGCACACGCCTGTAGTCCCAGCACTTTAGGA T C SLC12A6 Ensembl:ENSG00000140199 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs904291784 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_349344,RMVar_hsa_circ_45955 7698 RMVar_ID_7698 Human_SNP_ID_572930801 A-to-I Human chr15 - 34270606 34270606 34270606 TGGAGACGGGGTTTCACCATGTTGTCCAGTCTAGTCTCAAACTCCAAGCCTCAAGTGATCCGCCT TGGAGACGGGGTTTCACCATGTTGTCCAGTCTGGTCTCAAACTCCAAGCCTCAAGTGATCCGCCT T C SLC12A6 Ensembl:ENSG00000140199 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1194574495 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_349344,RMVar_hsa_circ_45955 7699 RMVar_ID_7699 Human_SNP_ID_572948933 A-to-I Human chr15 - 34342477 34342477 34342477 TCACTGCAACCTCCGCCTCCTGGGCTCAAACAATCCTTCTGCCTCAGCCTCCCGAGTAGTTGGGA TCACTGCAACCTCCGCCTCCTGGGCTCAAACAGTCCTTCTGCCTCAGCCTCCCGAGTAGTTGGGA T C NOP10 Ensembl:ENSG00000182117 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1253967889 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102468,RMVar_hsa_circ_170546 7700 RMVar_ID_7700 Human_SNP_ID_572949040 A-to-I Human chr15 - 34342820 34342820 34342820 AATTCTGGCGGGGCGCAGTGGCTCCCGCCTGTAATCCTAGCACTTTGGGAGGCCGAGGCGGGTGG AATTCTGGCGGGGCGCAGTGGCTCCCGCCTGTGATCCTAGCACTTTGGGAGGCCGAGGCGGGTGG T C NOP10 Ensembl:ENSG00000182117 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1310140162 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102468,RMVar_hsa_circ_170546 7701 RMVar_ID_7701 Human_SNP_ID_572960278 A-to-I Human chr15 - 34380392 34380392 34380392 TCTTCTTAATGTATTTAGTGAAGATCATAAGAAATCCTTTAAGAGTTTAAATGTCTCTGAAACAG TCTTCTTAATGTATTTAGTGAAGATCATAAGACATCCTTTAAGAGTTTAAATGTCTCTGAAACAG T G GOLGA8A Ensembl:ENSG00000175265 Protein coding exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs879264451 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_170549,RMVar_hsa_circ_80767 7702 RMVar_ID_7702 Human_SNP_ID_572984902 A-to-I Human chr15 - 34495433 34495433 34495433 GCCCGCAGTGTGATGCGCCGGTCACGCCGCTCAATGTCGAAGTAGCAGCTGGCATTCTTGGTGGA GCCCGCAGTGTGATGCGCCGGTCACGCCGCTCTATGTCGAAGTAGCAGCTGGCATTCTTGGTGGA T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1032481488 Functional Loss SNV dbSNP153 33..33 33 - - - 7703 RMVar_ID_7703 Human_SNP_ID_572984903 A-to-I Human chr15 - 34495433 34495433 34495433 GCCCGCAGTGTGATGCGCCGGTCACGCCGCTCAATGTCGAAGTAGCAGCTGGCATTCTTGGTGGA GCCCGCAGTGTGATGCGCCGGTCACGCCGCTCGATGTCGAAGTAGCAGCTGGCATTCTTGGTGGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1032481488 Functional Loss SNV dbSNP153 33..33 33 - - - 7704 RMVar_ID_7704 Human_SNP_ID_572992640 A-to-I Human chr15 - 34531994 34531994 34531994 ATCACTTTAATTTGACTCTCCCCACAGAAACAACAGAAGAAACAAGTGGAACATCAGCTGGAAGA ATCACTTTAATTTGACTCTCCCCACAGAAACAGCAGAAGAAACAAGTGGAACATCAGCTGGAAGA T C GOLGA8B Ensembl:ENSG00000215252 Protein coding CDS GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs765375876 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1580878,Human_Splice_Rec_1580879,Human_Splice_Rec_1580906,Human_Splice_Rec_1580907,Human_Splice_Rec_1580950,Human_Splice_Rec_1580951,Human_Splice_Rec_1580994,Human_Splice_Rec_1580995,Human_Splice_Rec_1581020,Human_Splice_Rec_1581021 7705 RMVar_ID_7705 Human_SNP_ID_572995077 A-to-I Human chr15 - 34553940 34553940 34553940 CTATTTAATTTAACAGCTCTACTGAGATGAAGAAAGAAAAAGAATACCTGCTCAGCTCCAGAGAC CTATTTAATTTAACAGCTCTACTGAGATGAAGTAAGAAAAAGAATACCTGCTCAGCTCCAGAGAC T A GOLGA8B Ensembl:ENSG00000215252 Protein coding exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1371656313 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_885350,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 7706 RMVar_ID_7706 Human_SNP_ID_572995078 A-to-I Human chr15 - 34553940 34553940 34553940 CTATTTAATTTAACAGCTCTACTGAGATGAAGAAAGAAAAAGAATACCTGCTCAGCTCCAGAGAC CTATTTAATTTAACAGCTCTACTGAGATGAAGGAAGAAAAAGAATACCTGCTCAGCTCCAGAGAC T C GOLGA8B Ensembl:ENSG00000215252 Protein coding exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1371656313 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_885350,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 7707 RMVar_ID_7707 Human_SNP_ID_573065695 A-to-I Human chr15 + 34850410 34850409 34850411 GGAGATGTGCTCACGCATAGTGGCTAGGGATTAAGAGACAAAGGCAACAGGAGCAGACACCAGGT GGAGATGTGCTCACGCATAGTGGCTAGGGATT__GAGACAAAGGCAACAGGAGCAGACACCAGGT TAA T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992823736 Functional Loss DEL dbSNP153 33..34 33 - - - 7708 RMVar_ID_7708 Human_SNP_ID_573065696 A-to-I Human chr15 + 34850410 34850410 34850410 GGAGATGTGCTCACGCATAGTGGCTAGGGATTAAGAGACAAAGGCAACAGGAGCAGACACCAGGT GGAGATGTGCTCACGCATAGTGGCTAGGGATTGAGAGACAAAGGCAACAGGAGCAGACACCAGGT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1207562602 Functional Loss SNV dbSNP153 33..33 33 - - - 7709 RMVar_ID_7709 Human_SNP_ID_573089886 A-to-I Human chr15 - 34950360 34950360 34950360 AAGAGGGCCGGGAGTGGTGGCTTACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGTGGA AAGAGGGCCGGGAGTGGTGGCTTACACCTGTAGTCCCAGCACTTTGGGAGGCCAAGGCGGGTGGA T C AQR Ensembl:ENSG00000021776 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs527741495 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121343,RMVar_hsa_circ_170569,RMVar_hsa_circ_115011,RMVar_hsa_circ_170586,RMVar_hsa_circ_170598,RMVar_hsa_circ_127020,RMVar_hsa_circ_82898,RMVar_hsa_circ_120855,RMVar_hsa_circ_170615,RMVar_hsa_circ_170616,RMVar_hsa_circ_265134,RMVar_hsa_circ_170625,RMVar_hsa_circ_305822,RMVar_hsa_circ_346696,RMVar_hsa_circ_125093,RMVar_hsa_circ_170624 7710 RMVar_ID_7710 Human_SNP_ID_573090459 A-to-I Human chr15 - 34952881 34952881 34952881 ATTAGAAAGATAATGCTCTTGGAATTTAGGTAAGTTATAAGGCATTCCATTGATGAAAGAGATAA ATTAGAAAGATAATGCTCTTGGAATTTAGGTACGTTATAAGGCATTCCATTGATGAAAGAGATAA T G AQR Ensembl:ENSG00000021776 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1206803618 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9345189,Human_RBP_ID_19067833,Human_RBP_ID_22650536 Human_Splice_Rec_1581158,Human_Splice_Rec_1581226,Human_Splice_Rec_1581300,Human_Splice_Rec_1581308 RMVar_hsa_circ_121343,RMVar_hsa_circ_170569,RMVar_hsa_circ_115011,RMVar_hsa_circ_170586,RMVar_hsa_circ_170598,RMVar_hsa_circ_127020,RMVar_hsa_circ_82898,RMVar_hsa_circ_120855,RMVar_hsa_circ_170615,RMVar_hsa_circ_170616,RMVar_hsa_circ_265134,RMVar_hsa_circ_170625,RMVar_hsa_circ_305822,RMVar_hsa_circ_346696,RMVar_hsa_circ_125093,RMVar_hsa_circ_170624 7711 RMVar_ID_7711 Human_SNP_ID_573126473 A-to-I Human chr15 - 35092762 35092762 35092762 TCTCCCAGGTTGTCACAGACATTCATCTCCTCAACTTCCCCATACTTCTCCCCCAGTTCTATAAA TCTCCCAGGTTGTCACAGACATTCATCTCCTCTACTTCCCCATACTTCTCCCCCAGTTCTATAAA T A - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs879220153 Functional Loss SNV dbSNP153 33..33 33 - - - 7712 RMVar_ID_7712 Human_SNP_ID_573126486 A-to-I Human chr15 - 35092817 35092817 35092817 CTTTTCCGCATCTTCCTCACGGGGAAGCTTGAAGTACACGTTCCCCACCAGGTGGTCTCCCAGGT CTTTTCCGCATCTTCCTCACGGGGAAGCTTGACGTACACGTTCCCCACCAGGTGGTCTCCCAGGT T G - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs878996918 Functional Loss SNV dbSNP153 33..33 33 - - - 7713 RMVar_ID_7713 Human_SNP_ID_573173135 A-to-I Human chr15 - 35298541 35298541 35298541 AAATCCACTGACTGAAATACTTAAGTGTCTTAATAAAGTGGTCCTACTAAGGAACATGGTTGGTG AAATCCACTGACTGAAATACTTAAGTGTCTTACTAAAGTGGTCCTACTAAGGAACATGGTTGGTG T G RBM17P4,DPH6 Ensembl:ENSG00000259585,Ensembl:ENSG00000134146 Pseudogene,Protein coding exon,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1424071726 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5567727,Human_RBP_ID_17368219 7714 RMVar_ID_7714 Human_SNP_ID_573518671 A-to-I Human chr15 + 36770639 36770639 36770639 CCCAGCTAATTTTTGTGTTTTTTGTTAGAGACAGGGTTTCACCATGTTGGCCAGGCGGTCTCAAA CCCAGCTAATTTTTGTGTTTTTTGTTAGAGACGGGGTTTCACCATGTTGGCCAGGCGGTCTCAAA A G C15orf41 Ensembl:ENSG00000186073 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs983177804 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99290,RMVar_hsa_circ_170635 7715 RMVar_ID_7715 Human_SNP_ID_573576314 A-to-I Human chr15 - 37017511 37017511 37017511 GCACTTCTGGGCTCAAGCGATCTTTGCACCTCAGCCTTCCAAGTAGCTGGGACTACAGGCATGAC GCACTTCTGGGCTCAAGCGATCTTTGCACCTCCGCCTTCCAAGTAGCTGGGACTACAGGCATGAC T G MEIS2 Ensembl:ENSG00000134138 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1434561224 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_170645,RMVar_hsa_circ_170648,RMVar_hsa_circ_318109,RMVar_hsa_circ_334033,RMVar_hsa_circ_328146,RMVar_hsa_circ_170649 7716 RMVar_ID_7716 Human_SNP_ID_574310147 A-to-I Human chr15 + 39972188 39972188 39972188 GGAGACCAGCCTGGGCAGTGTGGTGAAACCCTATCTCTACAAAAAATATAAAAATTAGCCAGGCC GGAGACCAGCCTGGGCAGTGTGGTGAAACCCTGTCTCTACAAAAAATATAAAAATTAGCCAGGCC A G EIF2AK4 Ensembl:ENSG00000128829 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs954885511 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36913,RMVar_hsa_circ_89240,RMVar_hsa_circ_275567,RMVar_hsa_circ_170841 7717 RMVar_ID_7717 Human_SNP_ID_574361236 A-to-I Human chr15 + 40171142 40171142 40171142 AATTTTTAATAGAGATGACTTCTCTCTCTGTTACCCAGGCTGGTCTTGAACTCCTGAGCTCAAGC AATTTTTAATAGAGATGACTTCTCTCTCTGTTGCCCAGGCTGGTCTTGAACTCCTGAGCTCAAGC A G BUB1B Ensembl:ENSG00000156970 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1011909133 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57449,RMVar_hsa_circ_170868,RMVar_hsa_circ_304852,RMVar_hsa_circ_330682,RMVar_hsa_circ_170867 7718 RMVar_ID_7718 Human_SNP_ID_574367751 A-to-I Human chr15 + 40198035 40198035 40198035 GGAAAATGAAAGTCCATTTTAGGGCCAGGCACAGTGGCTCACACCTGTAATCCCAGCACTTTGGG GGAAAATGAAAGTCCATTTTAGGGCCAGGCACCGTGGCTCACACCTGTAATCCCAGCACTTTGGG A C BUB1B Ensembl:ENSG00000156970 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1198559603 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7105,RMVar_hsa_circ_52119,RMVar_hsa_circ_318811,RMVar_hsa_circ_80030,RMVar_hsa_circ_25011,RMVar_hsa_circ_37594,RMVar_hsa_circ_170871,RMVar_hsa_circ_350386,RMVar_hsa_circ_376054,RMVar_hsa_circ_50270,RMVar_hsa_circ_67094,RMVar_hsa_circ_170872,RMVar_hsa_circ_170876,RMVar_hsa_circ_89266,RMVar_hsa_circ_367136,RMVar_hsa_circ_18787,RMVar_hsa_circ_283656,RMVar_hsa_circ_170877 7719 RMVar_ID_7719 Human_SNP_ID_574367752 A-to-I Human chr15 + 40198035 40198035 40198035 GGAAAATGAAAGTCCATTTTAGGGCCAGGCACAGTGGCTCACACCTGTAATCCCAGCACTTTGGG GGAAAATGAAAGTCCATTTTAGGGCCAGGCACGGTGGCTCACACCTGTAATCCCAGCACTTTGGG A G BUB1B Ensembl:ENSG00000156970 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1198559603 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7105,RMVar_hsa_circ_52119,RMVar_hsa_circ_318811,RMVar_hsa_circ_80030,RMVar_hsa_circ_25011,RMVar_hsa_circ_37594,RMVar_hsa_circ_170871,RMVar_hsa_circ_350386,RMVar_hsa_circ_376054,RMVar_hsa_circ_50270,RMVar_hsa_circ_67094,RMVar_hsa_circ_170872,RMVar_hsa_circ_170876,RMVar_hsa_circ_89266,RMVar_hsa_circ_367136,RMVar_hsa_circ_18787,RMVar_hsa_circ_283656,RMVar_hsa_circ_170877 7720 RMVar_ID_7720 Human_SNP_ID_574370417 A-to-I Human chr15 + 40208930 40208930 40208930 AATCAAACTCACTGGGCTCAGGTGATCCTCCTACCTCAGCCTCCCGAGTAGCTGGGACCACAACT AATCAAACTCACTGGGCTCAGGTGATCCTCCTCCCTCAGCCTCCCGAGTAGCTGGGACCACAACT A C BUB1B Ensembl:ENSG00000156970 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs966961197 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_52119,RMVar_hsa_circ_25011,RMVar_hsa_circ_376054,RMVar_hsa_circ_50270,RMVar_hsa_circ_67094,RMVar_hsa_circ_170872,RMVar_hsa_circ_170876,RMVar_hsa_circ_89266,RMVar_hsa_circ_59437,RMVar_hsa_circ_38143,RMVar_hsa_circ_22068,RMVar_hsa_circ_125647,RMVar_hsa_circ_31760,RMVar_hsa_circ_170881,RMVar_hsa_circ_303251,RMVar_hsa_circ_363499 7721 RMVar_ID_7721 Human_SNP_ID_574370418 A-to-I Human chr15 + 40208930 40208930 40208930 AATCAAACTCACTGGGCTCAGGTGATCCTCCTACCTCAGCCTCCCGAGTAGCTGGGACCACAACT AATCAAACTCACTGGGCTCAGGTGATCCTCCTTCCTCAGCCTCCCGAGTAGCTGGGACCACAACT A T BUB1B Ensembl:ENSG00000156970 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs966961197 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_52119,RMVar_hsa_circ_25011,RMVar_hsa_circ_376054,RMVar_hsa_circ_50270,RMVar_hsa_circ_67094,RMVar_hsa_circ_170872,RMVar_hsa_circ_170876,RMVar_hsa_circ_89266,RMVar_hsa_circ_59437,RMVar_hsa_circ_38143,RMVar_hsa_circ_22068,RMVar_hsa_circ_125647,RMVar_hsa_circ_31760,RMVar_hsa_circ_170881,RMVar_hsa_circ_303251,RMVar_hsa_circ_363499 7722 RMVar_ID_7722 Human_SNP_ID_574370511 A-to-I Human chr15 + 40209300 40209300 40209300 AAAATTAGCCGGGCATGGTGGCGGGTGTCTGTAGTCCCAGCTACTCTGGAGGCTGAGGCAGGAGA AAAATTAGCCGGGCATGGTGGCGGGTGTCTGTCGTCCCAGCTACTCTGGAGGCTGAGGCAGGAGA A C BUB1B Ensembl:ENSG00000156970 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs188626357 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_52119,RMVar_hsa_circ_25011,RMVar_hsa_circ_376054,RMVar_hsa_circ_50270,RMVar_hsa_circ_67094,RMVar_hsa_circ_170872,RMVar_hsa_circ_170876,RMVar_hsa_circ_89266,RMVar_hsa_circ_59437,RMVar_hsa_circ_38143,RMVar_hsa_circ_22068,RMVar_hsa_circ_125647,RMVar_hsa_circ_31760,RMVar_hsa_circ_170881,RMVar_hsa_circ_303251,RMVar_hsa_circ_363499 7723 RMVar_ID_7723 Human_SNP_ID_574371945 A-to-I Human chr15 + 40215351 40215351 40215351 AAAATTAGCCAGGTATGGTGGTGCATGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGAAGGAGA AAAATTAGCCAGGTATGGTGGTGCATGCCTGTCATCCCAGCTACTTGGGAGGCTGAGGAAGGAGA A C BUB1B Ensembl:ENSG00000156970 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1369117838 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25011,RMVar_hsa_circ_50270,RMVar_hsa_circ_67094,RMVar_hsa_circ_31760,RMVar_hsa_circ_89056,RMVar_hsa_circ_170882 7724 RMVar_ID_7724 Human_SNP_ID_574372023 A-to-I Human chr15 + 40215648 40215648 40215648 CAAGATAGCCAGCCGTGGTGGCAGGTGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGA CAAGATAGCCAGCCGTGGTGGCAGGTGCCTGTGGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGA A G BUB1B Ensembl:ENSG00000156970 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1566829317 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25011,RMVar_hsa_circ_50270,RMVar_hsa_circ_67094,RMVar_hsa_circ_31760,RMVar_hsa_circ_89056,RMVar_hsa_circ_170882 7725 RMVar_ID_7725 Human_SNP_ID_574372134 A-to-I Human chr15 + 40216177 40216177 40216177 ATTTTACAATTACACTGGGCATGGTGACTCACATCTGTAATCCCAGCACTTTGGGAGACCAAGGC ATTTTACAATTACACTGGGCATGGTGACTCACGTCTGTAATCCCAGCACTTTGGGAGACCAAGGC A G BUB1B Ensembl:ENSG00000156970 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1228201364 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6422089 RMVar_hsa_circ_25011,RMVar_hsa_circ_50270,RMVar_hsa_circ_67094,RMVar_hsa_circ_31760,RMVar_hsa_circ_89056,RMVar_hsa_circ_170882 7726 RMVar_ID_7726 Human_SNP_ID_574372148 A-to-I Human chr15 + 40216273 40216273 40216273 CAGTCTGGGCAATATAATGAGACCTCATCTCTACAAAAAATTAAGAAATTAGCCAGGCATGGTGG CAGTCTGGGCAATATAATGAGACCTCATCTCTGCAAAAAATTAAGAAATTAGCCAGGCATGGTGG A G BUB1B Ensembl:ENSG00000156970 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1285586789 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25011,RMVar_hsa_circ_50270,RMVar_hsa_circ_67094,RMVar_hsa_circ_31760,RMVar_hsa_circ_89056,RMVar_hsa_circ_170882 7727 RMVar_ID_7727 Human_SNP_ID_574372149 A-to-I Human chr15 + 40216273 40216273 40216273 CAGTCTGGGCAATATAATGAGACCTCATCTCTACAAAAAATTAAGAAATTAGCCAGGCATGGTGG CAGTCTGGGCAATATAATGAGACCTCATCTCTTCAAAAAATTAAGAAATTAGCCAGGCATGGTGG A T BUB1B Ensembl:ENSG00000156970 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1285586789 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25011,RMVar_hsa_circ_50270,RMVar_hsa_circ_67094,RMVar_hsa_circ_31760,RMVar_hsa_circ_89056,RMVar_hsa_circ_170882 7728 RMVar_ID_7728 Human_SNP_ID_574372159 A-to-I Human chr15 + 40216299 40216299 40216299 ATCTCTACAAAAAATTAAGAAATTAGCCAGGCATGGTGGCACACACCAGTAGTCCCAGCTACTCG ATCTCTACAAAAAATTAAGAAATTAGCCAGGCCTGGTGGCACACACCAGTAGTCCCAGCTACTCG A C BUB1B Ensembl:ENSG00000156970 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1476711214 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25011,RMVar_hsa_circ_50270,RMVar_hsa_circ_67094,RMVar_hsa_circ_31760,RMVar_hsa_circ_89056,RMVar_hsa_circ_170882 7729 RMVar_ID_7729 Human_SNP_ID_574372164 A-to-I Human chr15 + 40216307 40216307 40216307 AAAAAATTAAGAAATTAGCCAGGCATGGTGGCACACACCAGTAGTCCCAGCTACTCGGGAGGCTG AAAAAATTAAGAAATTAGCCAGGCATGGTGGCTCACACCAGTAGTCCCAGCTACTCGGGAGGCTG A T BUB1B Ensembl:ENSG00000156970 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1035467346 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25011,RMVar_hsa_circ_50270,RMVar_hsa_circ_67094,RMVar_hsa_circ_31760,RMVar_hsa_circ_89056,RMVar_hsa_circ_170882 7730 RMVar_ID_7730 Human_SNP_ID_574373025 A-to-I Human chr15 + 40219460 40219460 40219460 ACTTACTAAGTCAGCCGGGCATGGTGGCTCACACCTGTAATCACAGCACTTTGGGAGGCCGAGGC ACTTACTAAGTCAGCCGGGCATGGTGGCTCACGCCTGTAATCACAGCACTTTGGGAGGCCGAGGC A G BUB1B-PAK6,BUB1B,PAK6 Ensembl:ENSG00000259288,Ensembl:ENSG00000156970,Ensembl:ENSG00000137843 Protein coding,Protein coding,Protein coding intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1400582164 Functional Loss SNV dbSNP153 33..33 33 - - - 7731 RMVar_ID_7731 Human_SNP_ID_574373043 A-to-I Human chr15 + 40219534 40219534 40219534 GAGGTCAGGAGTTTGAGAGCAGCCTGGGCAACATGGCGAAACCTTGTCTCTACTCAAAATACAAG GAGGTCAGGAGTTTGAGAGCAGCCTGGGCAACGTGGCGAAACCTTGTCTCTACTCAAAATACAAG A G BUB1B-PAK6,BUB1B,PAK6 Ensembl:ENSG00000259288,Ensembl:ENSG00000156970,Ensembl:ENSG00000137843 Protein coding,Protein coding,Protein coding intron,intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1222153948 Functional Loss SNV dbSNP153 33..33 33 - - - 7732 RMVar_ID_7732 Human_SNP_ID_574375827 A-to-I Human chr15 + 40231395 40231395 40231395 CAACCAAGCTGGGCATGGTGGTTCACACCTGTAATCCCAGCTACTCACGAGGCTGAGGTGGGAGG CAACCAAGCTGGGCATGGTGGTTCACACCTGTCATCCCAGCTACTCACGAGGCTGAGGTGGGAGG A C BUB1B-PAK6,PAK6 Ensembl:ENSG00000259288,Ensembl:ENSG00000137843 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1032384136 Functional Loss SNV dbSNP153 33..33 33 - - - 7733 RMVar_ID_7733 Human_SNP_ID_574385470 A-to-I Human chr15 + 40267548 40267548 40267548 GGGCGCGGTGGCGGGCGCCTGTAGTCCAAGCTACTCAGGAGGCTGAGGCAGGAGAATGGCGTGAA GGGCGCGGTGGCGGGCGCCTGTAGTCCAAGCTGCTCAGGAGGCTGAGGCAGGAGAATGGCGTGAA A G PAK6 Ensembl:ENSG00000137843 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1192491298 Functional Loss SNV dbSNP153 33..33 33 - - - 7734 RMVar_ID_7734 Human_SNP_ID_574419234 A-to-I Human chr15 + 40387861 40387861 40387861 GGGACCCCATCTCTACTAAAAATACAAAAATTAGCCAGGCATGGTGGCGCATGTCTGTAATCCCA GGGACCCCATCTCTACTAAAAATACAAAAATTGGCCAGGCATGGTGGCGCATGTCTGTAATCCCA A G KNSTRN Ensembl:ENSG00000128944 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1201062582 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59058,RMVar_hsa_circ_11221,RMVar_hsa_circ_316189,RMVar_hsa_circ_44115,RMVar_hsa_circ_170892,RMVar_hsa_circ_170888,RMVar_hsa_circ_170889,RMVar_hsa_circ_299977,RMVar_hsa_circ_315451,RMVar_hsa_circ_170891,RMVar_hsa_circ_63787,RMVar_hsa_circ_170893,RMVar_hsa_circ_353325,RMVar_hsa_circ_366612 7735 RMVar_ID_7735 Human_SNP_ID_574419236 A-to-I Human chr15 + 40387869 40387869 40387869 ATCTCTACTAAAAATACAAAAATTAGCCAGGCATGGTGGCGCATGTCTGTAATCCCAGCTACTCA ATCTCTACTAAAAATACAAAAATTAGCCAGGCCTGGTGGCGCATGTCTGTAATCCCAGCTACTCA A C KNSTRN Ensembl:ENSG00000128944 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs539730346 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59058,RMVar_hsa_circ_11221,RMVar_hsa_circ_316189,RMVar_hsa_circ_44115,RMVar_hsa_circ_170892,RMVar_hsa_circ_170888,RMVar_hsa_circ_170889,RMVar_hsa_circ_299977,RMVar_hsa_circ_315451,RMVar_hsa_circ_170891,RMVar_hsa_circ_63787,RMVar_hsa_circ_170893,RMVar_hsa_circ_353325,RMVar_hsa_circ_366612 7736 RMVar_ID_7736 Human_SNP_ID_574419237 A-to-I Human chr15 + 40387869 40387869 40387869 ATCTCTACTAAAAATACAAAAATTAGCCAGGCATGGTGGCGCATGTCTGTAATCCCAGCTACTCA ATCTCTACTAAAAATACAAAAATTAGCCAGGCGTGGTGGCGCATGTCTGTAATCCCAGCTACTCA A G KNSTRN Ensembl:ENSG00000128944 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs539730346 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59058,RMVar_hsa_circ_11221,RMVar_hsa_circ_316189,RMVar_hsa_circ_44115,RMVar_hsa_circ_170892,RMVar_hsa_circ_170888,RMVar_hsa_circ_170889,RMVar_hsa_circ_299977,RMVar_hsa_circ_315451,RMVar_hsa_circ_170891,RMVar_hsa_circ_63787,RMVar_hsa_circ_170893,RMVar_hsa_circ_353325,RMVar_hsa_circ_366612 7737 RMVar_ID_7737 Human_SNP_ID_574419602 A-to-I Human chr15 + 40389212 40389212 40389212 TTGTTGCCACCCAGGCTGGAGTGCAATGGCGCAATCTCAGCTCACCACAACCTCCGCCTCCTGGG TTGTTGCCACCCAGGCTGGAGTGCAATGGCGCGATCTCAGCTCACCACAACCTCCGCCTCCTGGG A G KNSTRN Ensembl:ENSG00000128944 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1312116061 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1584400 RMVar_hsa_circ_59058,RMVar_hsa_circ_11221,RMVar_hsa_circ_316189,RMVar_hsa_circ_44115,RMVar_hsa_circ_170892,RMVar_hsa_circ_170888,RMVar_hsa_circ_170889,RMVar_hsa_circ_299977,RMVar_hsa_circ_315451,RMVar_hsa_circ_170891,RMVar_hsa_circ_63787,RMVar_hsa_circ_170893,RMVar_hsa_circ_353325,RMVar_hsa_circ_366612 7738 RMVar_ID_7738 Human_SNP_ID_574419603 A-to-I Human chr15 + 40389212 40389212 40389212 TTGTTGCCACCCAGGCTGGAGTGCAATGGCGCAATCTCAGCTCACCACAACCTCCGCCTCCTGGG TTGTTGCCACCCAGGCTGGAGTGCAATGGCGCTATCTCAGCTCACCACAACCTCCGCCTCCTGGG A T KNSTRN Ensembl:ENSG00000128944 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1312116061 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1584400 RMVar_hsa_circ_59058,RMVar_hsa_circ_11221,RMVar_hsa_circ_316189,RMVar_hsa_circ_44115,RMVar_hsa_circ_170892,RMVar_hsa_circ_170888,RMVar_hsa_circ_170889,RMVar_hsa_circ_299977,RMVar_hsa_circ_315451,RMVar_hsa_circ_170891,RMVar_hsa_circ_63787,RMVar_hsa_circ_170893,RMVar_hsa_circ_353325,RMVar_hsa_circ_366612 7739 RMVar_ID_7739 Human_SNP_ID_574419606 A-to-I Human chr15 + 40389218 40389218 40389218 CCACCCAGGCTGGAGTGCAATGGCGCAATCTCAGCTCACCACAACCTCCGCCTCCTGGGTTCAAG CCACCCAGGCTGGAGTGCAATGGCGCAATCTCGGCTCACCACAACCTCCGCCTCCTGGGTTCAAG A G KNSTRN Ensembl:ENSG00000128944 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1207382984 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1584400 RMVar_hsa_circ_59058,RMVar_hsa_circ_11221,RMVar_hsa_circ_316189,RMVar_hsa_circ_44115,RMVar_hsa_circ_170892,RMVar_hsa_circ_170888,RMVar_hsa_circ_170889,RMVar_hsa_circ_299977,RMVar_hsa_circ_315451,RMVar_hsa_circ_170891,RMVar_hsa_circ_63787,RMVar_hsa_circ_170893,RMVar_hsa_circ_353325,RMVar_hsa_circ_366612 7740 RMVar_ID_7740 Human_SNP_ID_574419648 A-to-I Human chr15 + 40389324 40389324 40389324 GCATGCGCCACCACGCCTGACTAATCTTTTGTAATTTTAGTAGAGACAGGGTTTCTCTTATCTTG GCATGCGCCACCACGCCTGACTAATCTTTTGTGATTTTAGTAGAGACAGGGTTTCTCTTATCTTG A G KNSTRN Ensembl:ENSG00000128944 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1191322989 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59058,RMVar_hsa_circ_11221,RMVar_hsa_circ_316189,RMVar_hsa_circ_44115,RMVar_hsa_circ_170892,RMVar_hsa_circ_170888,RMVar_hsa_circ_170889,RMVar_hsa_circ_299977,RMVar_hsa_circ_315451,RMVar_hsa_circ_170891,RMVar_hsa_circ_63787,RMVar_hsa_circ_170893,RMVar_hsa_circ_353325,RMVar_hsa_circ_366612 7741 RMVar_ID_7741 Human_SNP_ID_574419650 A-to-I Human chr15 + 40389330 40389330 40389330 GCCACCACGCCTGACTAATCTTTTGTAATTTTAGTAGAGACAGGGTTTCTCTTATCTTGGTCAGG GCCACCACGCCTGACTAATCTTTTGTAATTTTGGTAGAGACAGGGTTTCTCTTATCTTGGTCAGG A G KNSTRN Ensembl:ENSG00000128944 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1333241995 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59058,RMVar_hsa_circ_11221,RMVar_hsa_circ_316189,RMVar_hsa_circ_44115,RMVar_hsa_circ_170892,RMVar_hsa_circ_170888,RMVar_hsa_circ_170889,RMVar_hsa_circ_299977,RMVar_hsa_circ_315451,RMVar_hsa_circ_170891,RMVar_hsa_circ_63787,RMVar_hsa_circ_170893,RMVar_hsa_circ_353325,RMVar_hsa_circ_366612 7742 RMVar_ID_7742 Human_SNP_ID_574421189 A-to-I Human chr15 + 40394978 40394978 40394978 CACCACCACACCCAGCTAATTTTTGTATTTTTAGTAGAGGCGTGGTTTCACCATGTTGGCCAACT CACCACCACACCCAGCTAATTTTTGTATTTTTTGTAGAGGCGTGGTTTCACCATGTTGGCCAACT A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1173215559 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12497260 7743 RMVar_ID_7743 Human_SNP_ID_574421248 A-to-I Human chr15 + 40395205 40395193 40395206 CAGCCTCCCAAAATGCTGGGATTACAGGCGTGAGCCACCACGCCCAGCCCTCCCTGCACTCTTAA CAGCCTCCCAAAATGCTGGGA_____________CCACCACGCCCAGCCCTCCCTGCACTCTTAA ATTACAGGCGTGAG A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1047922870 Functional Loss DEL dbSNP153 22..34 33 - - - 7744 RMVar_ID_7744 Human_SNP_ID_574421380 A-to-I Human chr15 + 40395706 40395706 40395706 CATGCCTGTAATCCTGACACTTCGGGAGGCTGAAGTGGGTGGATCACGATGTCAGGAGTTAGAGA CATGCCTGTAATCCTGACACTTCGGGAGGCTGTAGTGGGTGGATCACGATGTCAGGAGTTAGAGA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1566925067 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6422374 7745 RMVar_ID_7745 Human_SNP_ID_574421389 A-to-I Human chr15 + 40395747 40395747 40395747 GATCACGATGTCAGGAGTTAGAGATCAGCCTGACCATCATGATGAAACCCTGTCTCTACTAAAAA GATCACGATGTCAGGAGTTAGAGATCAGCCTGGCCATCATGATGAAACCCTGTCTCTACTAAAAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1241865676 Functional Loss SNV dbSNP153 33..33 33 - - - 7746 RMVar_ID_7746 Human_SNP_ID_574421587 A-to-I Human chr15 + 40396600 40396598 40396600 TTTAAAATGGTTGAGGCCGGGTGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAG TTTAAAATGGTTGAGGCCGGGTGCGGTGGCT__CACCTGTAATCCCAGCACTTTGGGAGGCCAAG TCA T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049134910 Functional Loss DEL dbSNP153 32..33 33 - - - 7747 RMVar_ID_7747 Human_SNP_ID_574421588 A-to-I Human chr15 + 40396602 40396602 40396602 TAAAATGGTTGAGGCCGGGTGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGT TAAAATGGTTGAGGCCGGGTGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1035389074 Functional Loss SNV dbSNP153 33..33 33 - - - 7748 RMVar_ID_7748 Human_SNP_ID_574421624 A-to-I Human chr15 + 40396739 40396738 40396739 CAAAAATTAGCCGGTTGTGGTGGCGGGTGCCTATAGTCGCAGCTACTTGGGTGGCTGAGGCAGGA CAAAAATTAGCCGGTTGTGGTGGCGGGTGCCT_TAGTCGCAGCTACTTGGGTGGCTGAGGCAGGA TA T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1362222483 Functional Loss DEL dbSNP153 33..33 33 - - - 7749 RMVar_ID_7749 Human_SNP_ID_574421625 A-to-I Human chr15 + 40396739 40396739 40396739 CAAAAATTAGCCGGTTGTGGTGGCGGGTGCCTATAGTCGCAGCTACTTGGGTGGCTGAGGCAGGA CAAAAATTAGCCGGTTGTGGTGGCGGGTGCCTTTAGTCGCAGCTACTTGGGTGGCTGAGGCAGGA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs892799463 Functional Loss SNV dbSNP153 33..33 33 - - - 7750 RMVar_ID_7750 Human_SNP_ID_574421628 A-to-I Human chr15 + 40396741 40396741 40396741 AAAATTAGCCGGTTGTGGTGGCGGGTGCCTATAGTCGCAGCTACTTGGGTGGCTGAGGCAGGAGA AAAATTAGCCGGTTGTGGTGGCGGGTGCCTATGGTCGCAGCTACTTGGGTGGCTGAGGCAGGAGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs552362415 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_456588 7751 RMVar_ID_7751 Human_SNP_ID_574421762 A-to-I Human chr15 + 40397200 40397200 40397200 GACCTCCTGGGCTCAAGTGATCCTCCTGCCTCAGCCCCCCAAGTAACTGGGACTACAGGCACACA GACCTCCTGGGCTCAAGTGATCCTCCTGCCTCTGCCCCCCAAGTAACTGGGACTACAGGCACACA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1047973146 Functional Loss SNV dbSNP153 33..33 33 - - - 7752 RMVar_ID_7752 Human_SNP_ID_574421935 A-to-I Human chr15 + 40397678 40397678 40397678 TTTTTAAATTTTTGGTAGAGCTGGGGGCTCTCACTATGTTGCCCAGGCTGATCTTGAACTCCTGG TTTTTAAATTTTTGGTAGAGCTGGGGGCTCTCGCTATGTTGCCCAGGCTGATCTTGAACTCCTGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1184360925 Functional Loss SNV dbSNP153 33..33 33 - - - 7753 RMVar_ID_7753 Human_SNP_ID_574422024 A-to-I Human chr15 + 40398065 40398065 40398065 GGCCAGACACAGTGGCTCATGCTTGTAATCCCAGCACTTTGGAAGACTGGGGCGGGAGGAGTACT GGCCAGACACAGTGGCTCATGCTTGTAATCCCGGCACTTTGGAAGACTGGGGCGGGAGGAGTACT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1481538021 Functional Loss SNV dbSNP153 33..33 33 - - - 7754 RMVar_ID_7754 Human_SNP_ID_574423297 A-to-I Human chr15 + 40402225 40402225 40402225 AGGAGATAGGGTCTTTCTATGTTGCCCAGACTAGACTCCAACCCCTGGGCTCAAGCAATCCTCCT AGGAGATAGGGTCTTTCTATGTTGCCCAGACTCGACTCCAACCCCTGGGCTCAAGCAATCCTCCT A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1201474511 Functional Loss SNV dbSNP153 33..33 33 - - - 7755 RMVar_ID_7755 Human_SNP_ID_574460237 A-to-I Human chr15 - 40545864 40545864 40545864 TAGTTACATGAATGAGGTGTGGCGGCAAGGCTAGAGAGAAGTGGATATGGGAGCATTTGCAAGGA TAGTTACATGAATGAGGTGTGGCGGCAAGGCTGGAGAGAAGTGGATATGGGAGCATTTGCAAGGA T C CCDC32 Ensembl:ENSG00000128891 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs544521764 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12497996 7756 RMVar_ID_7756 Human_SNP_ID_574460324 A-to-I Human chr15 - 40546254 40546254 40546254 CCAGAAGGCGGAGGTTGCAGTGAGCCAAGATCATGCCACTGCCCTCCAGCCTGGGTGACAGGGTG CCAGAAGGCGGAGGTTGCAGTGAGCCAAGATCGTGCCACTGCCCTCCAGCCTGGGTGACAGGGTG T C CCDC32 Ensembl:ENSG00000128891 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1371046674 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25185056 7757 RMVar_ID_7757 Human_SNP_ID_574461353 A-to-I Human chr15 - 40551368 40551368 40551368 GGATGGATTTTTTTGTTTTGAGATGGAGTCTCACTCTCTTGCCCAGGCTGGAGTGCAGTGGCGCC GGATGGATTTTTTTGTTTTGAGATGGAGTCTCGCTCTCTTGCCCAGGCTGGAGTGCAGTGGCGCC T C CCDC32 Ensembl:ENSG00000128891 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1311716862 Functional Loss SNV dbSNP153 33..33 33 - - - 7758 RMVar_ID_7758 Human_SNP_ID_574461426 A-to-I Human chr15 - 40551745 40551745 40551745 TGGAGGGCAGTGGCACGGTCTCAGCTCACTGCAGTCTTGACCTCCTGGGCTCAGGTGATCCTGCC TGGAGGGCAGTGGCACGGTCTCAGCTCACTGCGGTCTTGACCTCCTGGGCTCAGGTGATCCTGCC T C CCDC32 Ensembl:ENSG00000128891 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1566982072 Functional Loss SNV dbSNP153 33..33 33 - - - 7759 RMVar_ID_7759 Human_SNP_ID_574467171 A-to-I Human chr15 + 40573128 40573128 40573128 CTCACTGCAACCTCCGCCTCCTGGGTTCAAGCAATTATCCTGCCTCAGCCTCCCAGGTAGCTGGG CTCACTGCAACCTCCGCCTCCTGGGTTCAAGCGATTATCCTGCCTCAGCCTCCCAGGTAGCTGGG A G RPUSD2 Ensembl:ENSG00000166133 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1237331788 Functional Loss SNV dbSNP153 33..33 33 - - - 7760 RMVar_ID_7760 Human_SNP_ID_574467190 A-to-I Human chr15 + 40573205 40573205 40573205 CGCCACCACGCCTGGCTAATTTTGTATTTTTTAGTAGAGACGGGGTTTCTTCATGTTGGTCAGGC CGCCACCACGCCTGGCTAATTTTGTATTTTTTGGTAGAGACGGGGTTTCTTCATGTTGGTCAGGC A G RPUSD2 Ensembl:ENSG00000166133 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1054931992 Functional Loss SNV dbSNP153 33..33 33 - - - 7761 RMVar_ID_7761 Human_SNP_ID_574472598 A-to-I Human chr15 - 40593840 40593840 40593840 CTAATCCATTGTGCTCTGCACGCGTGGGTTCGAATCCCATCCTCGTCGATGTGGTGGCTTACTTT CTAATCCATTGTGCTCTGCACGCGTGGGTTCGCATCCCATCCTCGTCGATGTGGTGGCTTACTTT T G tRNA-Ser-GCT-4-2 RNACentral:URS00002034DC tRNA intron GSE100210 HepG2 cell line - 29129909 RNA-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 7762 RMVar_ID_7762 Human_SNP_ID_574481997 A-to-I Human chr15 + 40627094 40627094 40627094 TCTTTGTATTTTCAGTAGAGTCAGGGTTTCACAATGTTGGCCAGGCTGGTCTTAAACTCCTGATC TCTTTGTATTTTCAGTAGAGTCAGGGTTTCACCATGTTGGCCAGGCTGGTCTTAAACTCCTGATC A C KNL1 Ensembl:ENSG00000137812 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1399002286 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25136006 RMVar_hsa_circ_68971,RMVar_hsa_circ_113580,RMVar_hsa_circ_170912,RMVar_hsa_circ_101858,RMVar_hsa_circ_71997,RMVar_hsa_circ_339715,RMVar_hsa_circ_265957,RMVar_hsa_circ_170915,RMVar_hsa_circ_71883,RMVar_hsa_circ_122680,RMVar_hsa_circ_170916,RMVar_hsa_circ_170917,RMVar_hsa_circ_61350,RMVar_hsa_circ_118473,RMVar_hsa_circ_170918 7763 RMVar_ID_7763 Human_SNP_ID_574485159 A-to-I Human chr15 + 40639089 40639089 40639089 TGCTGGGATTACAGGCATGAGCCTCTGCACCCAGCCTGCCATTTCTTTTTTAACCAGTACATATA TGCTGGGATTACAGGCATGAGCCTCTGCACCCGGCCTGCCATTTCTTTTTTAACCAGTACATATA A G KNL1 Ensembl:ENSG00000137812 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs8031057 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4069,RMVar_hsa_circ_113580,RMVar_hsa_circ_170912,RMVar_hsa_circ_59934,RMVar_hsa_circ_101858,RMVar_hsa_circ_71997,RMVar_hsa_circ_265957,RMVar_hsa_circ_71883,RMVar_hsa_circ_122680,RMVar_hsa_circ_170916,RMVar_hsa_circ_170917,RMVar_hsa_circ_61350,RMVar_hsa_circ_329968,RMVar_hsa_circ_51206,RMVar_hsa_circ_55045,RMVar_hsa_circ_9243,RMVar_hsa_circ_364494,RMVar_hsa_circ_170919,RMVar_hsa_circ_74030,RMVar_hsa_circ_56729,RMVar_hsa_circ_96755,RMVar_hsa_circ_170920 7764 RMVar_ID_7764 Human_SNP_ID_574485160 A-to-I Human chr15 + 40639089 40639089 40639089 TGCTGGGATTACAGGCATGAGCCTCTGCACCCAGCCTGCCATTTCTTTTTTAACCAGTACATATA TGCTGGGATTACAGGCATGAGCCTCTGCACCCTGCCTGCCATTTCTTTTTTAACCAGTACATATA A T KNL1 Ensembl:ENSG00000137812 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs8031057 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4069,RMVar_hsa_circ_113580,RMVar_hsa_circ_170912,RMVar_hsa_circ_59934,RMVar_hsa_circ_101858,RMVar_hsa_circ_71997,RMVar_hsa_circ_265957,RMVar_hsa_circ_71883,RMVar_hsa_circ_122680,RMVar_hsa_circ_170916,RMVar_hsa_circ_170917,RMVar_hsa_circ_61350,RMVar_hsa_circ_329968,RMVar_hsa_circ_51206,RMVar_hsa_circ_55045,RMVar_hsa_circ_9243,RMVar_hsa_circ_364494,RMVar_hsa_circ_170919,RMVar_hsa_circ_74030,RMVar_hsa_circ_56729,RMVar_hsa_circ_96755,RMVar_hsa_circ_170920 7765 RMVar_ID_7765 Human_SNP_ID_574491044 A-to-I Human chr15 + 40660092 40660092 40660092 CGCCACCACACCTAGCTAATTTTTGCATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCTAGG CGCCACCACACCTAGCTAATTTTTGCATTTTTGGTAGAGATGGGGTTTCACCATGTTGGCCTAGG A G KNL1 Ensembl:ENSG00000137812 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs991777642 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265957 7766 RMVar_ID_7766 Human_SNP_ID_574491255 A-to-I Human chr15 + 40660918 40660918 40660918 CTGGGAGGTGGAGATTGTGGTGAGCCAGGATCATGCCACTGGCCTCCAGCCTGGGTGACAGAACC CTGGGAGGTGGAGATTGTGGTGAGCCAGGATCTTGCCACTGGCCTCCAGCCTGGGTGACAGAACC A T KNL1 Ensembl:ENSG00000137812 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs906393727 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265957 7767 RMVar_ID_7767 Human_SNP_ID_574491803 A-to-I Human chr15 + 40662758 40662743 40662759 AAAATGGGTGAATAGCCTGAGTCCAGGAATTCAAGACCAGCCTGGGCAACATGGCAAAACCCCAC AAAATGGGTGAATAGCCT________________GACCAGCCTGGGCAACATGGCAAAACCCCAC TGAGTCCAGGAATTCAA T KNL1 Ensembl:ENSG00000137812 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1567025819 Functional Loss DEL dbSNP153 19..34 33 - - - 7768 RMVar_ID_7768 Human_SNP_ID_574491815 A-to-I Human chr15 + 40662797 40662796 40662797 GCCTGGGCAACATGGCAAAACCCCACCTCTACAAAAAATACGAAAGTTAGCCAGTCATGGTGGCT GCCTGGGCAACATGGCAAAACCCCACCTCTAC_AAAAATACGAAAGTTAGCCAGTCATGGTGGCT CA C KNL1 Ensembl:ENSG00000137812 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1036203311 Functional Loss DEL dbSNP153 33..33 33 - - - 7769 RMVar_ID_7769 Human_SNP_ID_574491816 A-to-I Human chr15 + 40662797 40662797 40662797 GCCTGGGCAACATGGCAAAACCCCACCTCTACAAAAAATACGAAAGTTAGCCAGTCATGGTGGCT GCCTGGGCAACATGGCAAAACCCCACCTCTACTAAAAATACGAAAGTTAGCCAGTCATGGTGGCT A T KNL1 Ensembl:ENSG00000137812 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1039533635 Functional Loss SNV dbSNP153 33..33 33 - - - 7770 RMVar_ID_7770 Human_SNP_ID_574491817 A-to-I Human chr15 + 40662800 40662800 40662800 TGGGCAACATGGCAAAACCCCACCTCTACAAAAAATACGAAAGTTAGCCAGTCATGGTGGCTTGC TGGGCAACATGGCAAAACCCCACCTCTACAAAGAATACGAAAGTTAGCCAGTCATGGTGGCTTGC A G KNL1 Ensembl:ENSG00000137812 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1403067377 Functional Loss SNV dbSNP153 33..33 33 - - - 7771 RMVar_ID_7771 Human_SNP_ID_574491908 A-to-I Human chr15 + 40663177 40663177 40663177 CGCCTCCTGGGTTCACGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGTGCCCA CGCCTCCTGGGTTCACGCCATTCTCCTGCCTCCGCCTCCCGAGTAGCTGGGACTACAGGTGCCCA A C KNL1 Ensembl:ENSG00000137812 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1035354988 Functional Loss SNV dbSNP153 33..33 33 - - - 7772 RMVar_ID_7772 Human_SNP_ID_574491938 A-to-I Human chr15 + 40663258 40663258 40663258 ATTTTTTGTCTTTTTAGTAGAAATGGGGTTTCACGATGTTAGCCAGGATGGTCTCGATCTCCTGA ATTTTTTGTCTTTTTAGTAGAAATGGGGTTTCTCGATGTTAGCCAGGATGGTCTCGATCTCCTGA A T KNL1 Ensembl:ENSG00000137812 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs919332857 Functional Loss SNV dbSNP153 33..33 33 - - - 7773 RMVar_ID_7773 Human_SNP_ID_574491964 A-to-I Human chr15 + 40663317 40663317 40663317 TCCTGACCTCGTGATCCGCCTGCCTCGGCTTCAAAGTGCTGGGATTACAGGTGTGAGCCACCACA TCCTGACCTCGTGATCCGCCTGCCTCGGCTTCGAAGTGCTGGGATTACAGGTGTGAGCCACCACA A G KNL1 Ensembl:ENSG00000137812 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs939950396 Functional Loss SNV dbSNP153 33..33 33 - - - 7774 RMVar_ID_7774 Human_SNP_ID_574491967 A-to-I Human chr15 + 40663331 40663331 40663331 TCCGCCTGCCTCGGCTTCAAAGTGCTGGGATTACAGGTGTGAGCCACCACACCCAGCAATGTTTT TCCGCCTGCCTCGGCTTCAAAGTGCTGGGATTCCAGGTGTGAGCCACCACACCCAGCAATGTTTT A C KNL1 Ensembl:ENSG00000137812 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1321897085 Functional Loss SNV dbSNP153 33..33 33 - - - 7775 RMVar_ID_7775 Human_SNP_ID_574499126 A-to-I Human chr15 - 40688598 40688598 40688598 GGAGTGCAGTGGCGCGATCTTGGCTCACTGCAACCTCTACCTCCTGGGTTCAAGCAATCCTCCTG GGAGTGCAGTGGCGCGATCTTGGCTCACTGCATCCTCTACCTCCTGGGTTCAAGCAATCCTCCTG T A RAD51-AS1 Ensembl:ENSG00000245849 lincRNA intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1197370866 Functional Loss SNV dbSNP153 33..33 33 - - - 7776 RMVar_ID_7776 Human_SNP_ID_574499671 A-to-I Human chr15 - 40690601 40690601 40690601 GGGAGATTGCTTGAGCCCAGGAGTTCAAGGTTACAGTGAGCTATGATTGCACCTTGCACCACTGC GGGAGATTGCTTGAGCCCAGGAGTTCAAGGTTTCAGTGAGCTATGATTGCACCTTGCACCACTGC T A RAD51-AS1 Ensembl:ENSG00000245849 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1276029559 Functional Loss SNV dbSNP153 33..33 33 - - - 7777 RMVar_ID_7777 Human_SNP_ID_574499672 A-to-I Human chr15 - 40690601 40690601 40690601 GGGAGATTGCTTGAGCCCAGGAGTTCAAGGTTACAGTGAGCTATGATTGCACCTTGCACCACTGC GGGAGATTGCTTGAGCCCAGGAGTTCAAGGTTGCAGTGAGCTATGATTGCACCTTGCACCACTGC T C RAD51-AS1 Ensembl:ENSG00000245849 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1276029559 Functional Loss SNV dbSNP153 33..33 33 - - - 7778 RMVar_ID_7778 Human_SNP_ID_574499679 A-to-I Human chr15 - 40690620 40690620 40690620 TGTCTGGGAAGCTGAGGAGGGGAGATTGCTTGAGCCCAGGAGTTCAAGGTTACAGTGAGCTATGA TGTCTGGGAAGCTGAGGAGGGGAGATTGCTTGTGCCCAGGAGTTCAAGGTTACAGTGAGCTATGA T A RAD51-AS1 Ensembl:ENSG00000245849 lincRNA intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs573328046 Functional Loss SNV dbSNP153 33..33 33 - - - 7779 RMVar_ID_7779 Human_SNP_ID_574499720 A-to-I Human chr15 - 40690750 40690750 40690750 CTCCAGACCTCATGATCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGACGTGAGCCACCGCGC CTCCAGACCTCATGATCCGCCTCGGCCTCCCAGAGTGCTGGGATTACAGACGTGAGCCACCGCGC T C RAD51-AS1 Ensembl:ENSG00000245849 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1034055740 Functional Loss SNV dbSNP153 33..33 33 - - - 7780 RMVar_ID_7780 Human_SNP_ID_574499721 A-to-I Human chr15 - 40690750 40690750 40690750 CTCCAGACCTCATGATCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGACGTGAGCCACCGCGC CTCCAGACCTCATGATCCGCCTCGGCCTCCCACAGTGCTGGGATTACAGACGTGAGCCACCGCGC T G RAD51-AS1 Ensembl:ENSG00000245849 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1034055740 Functional Loss SNV dbSNP153 33..33 33 - - - 7781 RMVar_ID_7781 Human_SNP_ID_574500024 A-to-I Human chr15 - 40691600 40691600 40691600 AAACTGGGAGGCAGAGGTTGCAGTGAGCTGAGATCGTGCCACTGCACTCCAGCCTGGATGACAGA AAACTGGGAGGCAGAGGTTGCAGTGAGCTGAGGTCGTGCCACTGCACTCCAGCCTGGATGACAGA T C RAD51-AS1 Ensembl:ENSG00000245849 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1295706691 Functional Loss SNV dbSNP153 33..33 33 - - - 7782 RMVar_ID_7782 Human_SNP_ID_574500030 A-to-I Human chr15 - 40691630 40691630 40691630 CGCAGGAGGCCAAGGCAGGAGAATCGCATGAAACTGGGAGGCAGAGGTTGCAGTGAGCTGAGATC CGCAGGAGGCCAAGGCAGGAGAATCGCATGAACCTGGGAGGCAGAGGTTGCAGTGAGCTGAGATC T G RAD51-AS1 Ensembl:ENSG00000245849 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928485588 Functional Loss SNV dbSNP153 33..33 33 - - - 7783 RMVar_ID_7783 Human_SNP_ID_574500327 A-to-I Human chr15 - 40692778 40692778 40692778 CTGTTCAAGTTGGCCTTGAACTCCTGGCCTCAAGTGATCCTCCCACCTTGGCCTCCCAAAGTGTT CTGTTCAAGTTGGCCTTGAACTCCTGGCCTCAGGTGATCCTCCCACCTTGGCCTCCCAAAGTGTT T C RAD51-AS1 Ensembl:ENSG00000245849 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1354644945 Functional Loss SNV dbSNP153 33..33 33 - - - 7784 RMVar_ID_7784 Human_SNP_ID_574500552 A-to-I Human chr15 - 40693525 40693525 40693525 GGAGAGGCCAGGCGCGGTGGCTCAAGCCTGTAATCCCAGAACTTTGGGAGGCCAAGGTGGGCGGA GGAGAGGCCAGGCGCGGTGGCTCAAGCCTGTAGTCCCAGAACTTTGGGAGGCCAAGGTGGGCGGA T C RAD51-AS1 Ensembl:ENSG00000245849 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904872123 Functional Loss SNV dbSNP153 33..33 33 - - - 7785 RMVar_ID_7785 Human_SNP_ID_574500558 A-to-I Human chr15 - 40693548 40693548 40693548 AGCGACAACAACAAAACATGTAAGGAGAGGCCAGGCGCGGTGGCTCAAGCCTGTAATCCCAGAAC AGCGACAACAACAAAACATGTAAGGAGAGGCCGGGCGCGGTGGCTCAAGCCTGTAATCCCAGAAC T C RAD51-AS1 Ensembl:ENSG00000245849 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1359494476 Functional Loss SNV dbSNP153 33..33 33 - - - 7786 RMVar_ID_7786 Human_SNP_ID_574500611 A-to-I Human chr15 - 40693735 40693734 40693736 CCCCATATCTCAAAAAAAAAAAAAAAAAAAATAAGCTGGGCGTGGTGGCTTGTGCCTGTGGTCTC CCCCATATCTCAAAAAAAAAAAAAAAAAAAA__AGCTGGGCGTGGTGGCTTGTGCCTGTGGTCTC TTA T RAD51-AS1 Ensembl:ENSG00000245849 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1446472196 Functional Loss DEL dbSNP153 32..33 33 - - - 7787 RMVar_ID_7787 Human_SNP_ID_574500795 A-to-I Human chr15 - 40694294 40694294 40694294 CCAGTAATCCCAGCAGTTTAGGAGGCCAAGGCAGGCGGATCACCTGAGGTCAGGGGTTGGAGATA CCAGTAATCCCAGCAGTTTAGGAGGCCAAGGCTGGCGGATCACCTGAGGTCAGGGGTTGGAGATA T A RAD51-AS1 Ensembl:ENSG00000245849 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1265368569 Functional Loss SNV dbSNP153 33..33 33 - - - 7788 RMVar_ID_7788 Human_SNP_ID_574500797 A-to-I Human chr15 - 40694307 40694307 40694307 GCGGTGGTTCACGCCAGTAATCCCAGCAGTTTAGGAGGCCAAGGCAGGCGGATCACCTGAGGTCA GCGGTGGTTCACGCCAGTAATCCCAGCAGTTTTGGAGGCCAAGGCAGGCGGATCACCTGAGGTCA T A RAD51-AS1 Ensembl:ENSG00000245849 lincRNA intron GSE47997;GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831 K562 cells&HepG2 cells;HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line - 23474544,29129909,31158229,31158229,32596459 RNA-Seq:(High) rs1284934159 Functional Loss SNV dbSNP153 33..33 33 - - - 7789 RMVar_ID_7789 Human_SNP_ID_574500801 A-to-I Human chr15 - 40694324 40694324 40694324 GCTGAGTAGGGCCGGGCGCGGTGGTTCACGCCAGTAATCCCAGCAGTTTAGGAGGCCAAGGCAGG GCTGAGTAGGGCCGGGCGCGGTGGTTCACGCCGGTAATCCCAGCAGTTTAGGAGGCCAAGGCAGG T C RAD51-AS1 Ensembl:ENSG00000245849 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1360827295 Functional Loss SNV dbSNP153 33..33 33 - - - 7790 RMVar_ID_7790 Human_SNP_ID_574505214 A-to-I Human chr15 + 40709574 40709574 40709574 TTTTGTGTTTTTAGTAGAGAGGGGGTTTCACCATGTTGGCCAGGCTCCTCTTGAACTCCTGATCT TTTTGTGTTTTTAGTAGAGAGGGGGTTTCACCGTGTTGGCCAGGCTCCTCTTGAACTCCTGATCT A G RAD51 Ensembl:ENSG00000051180 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1321940077 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13886,RMVar_hsa_circ_13728,RMVar_hsa_circ_23170,RMVar_hsa_circ_27115,RMVar_hsa_circ_370580,RMVar_hsa_circ_170937,RMVar_hsa_circ_313576,RMVar_hsa_circ_295775,RMVar_hsa_circ_170938 7791 RMVar_ID_7791 Human_SNP_ID_574516411 A-to-I Human chr15 - 40748728 40748728 40748728 GGGCGTGGTGGTGCATGCCTGTAATCCCAGCTATTCCGGAGGCTGAGGCAGGAGAATCACTTGAA GGGCGTGGTGGTGCATGCCTGTAATCCCAGCTGTTCCGGAGGCTGAGGCAGGAGAATCACTTGAA T C RMDN3 Ensembl:ENSG00000137824 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1193383597 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93545,RMVar_hsa_circ_372955,RMVar_hsa_circ_170950,RMVar_hsa_circ_170951 7792 RMVar_ID_7792 Human_SNP_ID_574516557 A-to-I Human chr15 - 40749296 40749296 40749296 TTGCCCAGCCTGTTCTTGAACTCTTGGCCTCAAGCAGTTCTCCCACATCAGCCTCCAAGTGCTGA TTGCCCAGCCTGTTCTTGAACTCTTGGCCTCAGGCAGTTCTCCCACATCAGCCTCCAAGTGCTGA T C RMDN3 Ensembl:ENSG00000137824 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs952174551 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93545,RMVar_hsa_circ_372955,RMVar_hsa_circ_170950,RMVar_hsa_circ_170951 7793 RMVar_ID_7793 Human_SNP_ID_574516908 A-to-I Human chr15 - 40750588 40750588 40750588 ATCAGTCCAGGTGTGGTGGTGGCTCATGGGTAATCCCAGCACTTTGGGAGGCCGAGACAGGAGGA ATCAGTCCAGGTGTGGTGGTGGCTCATGGGTAGTCCCAGCACTTTGGGAGGCCGAGACAGGAGGA T C RMDN3 Ensembl:ENSG00000137824 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs780834851 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5354862 RMVar_hsa_circ_93545,RMVar_hsa_circ_372955,RMVar_hsa_circ_170950,RMVar_hsa_circ_170951 7794 RMVar_ID_7794 Human_SNP_ID_574520030 A-to-I Human chr15 - 40762315 40762315 40762315 TACTCGGGAGGCTGAGGCAGGAGAATGGCGTGAACCTGGGAGGCGGAGCTTGCAGTGAGCCGAGA TACTCGGGAGGCTGAGGCAGGAGAATGGCGTGGACCTGGGAGGCGGAGCTTGCAGTGAGCCGAGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs961281703 Functional Loss SNV dbSNP153 33..33 33 - - - 7795 RMVar_ID_7795 Human_SNP_ID_574520075 A-to-I Human chr15 - 40762447 40762447 40762447 TTGGGAGGCCGAGGCGGGCGGATCACGAGGTCAGGAAATCGAGACCATCCTGGCTTAACACAGTG TTGGGAGGCCGAGGCGGGCGGATCACGAGGTCCGGAAATCGAGACCATCCTGGCTTAACACAGTG T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232230257 Functional Loss SNV dbSNP153 33..33 33 - - - 7796 RMVar_ID_7796 Human_SNP_ID_574529970 A-to-I Human chr15 - 40800222 40800222 40800222 CTCTACTAAAAATACAAAAATTAGCTGGGCGTAGTGGCAGTTGCCTGTAGTCTCATGTACTCGAG CTCTACTAAAAATACAAAAATTAGCTGGGCGTGGTGGCAGTTGCCTGTAGTCTCATGTACTCGAG T C DNAJC17 Ensembl:ENSG00000104129 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1390037781 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125059,RMVar_hsa_circ_170959 7797 RMVar_ID_7797 Human_SNP_ID_574558313 A-to-I Human chr15 + 40904320 40904320 40904320 CAAGAATTTTCTTGGAGTCGCCCGGGCATGGTAGCTCACGCCTATAATCCCAGCACTTTGGGAGG CAAGAATTTTCTTGGAGTCGCCCGGGCATGGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs538348601 Functional Loss SNV dbSNP153 33..33 33 - - - 7798 RMVar_ID_7798 Human_SNP_ID_574558340 A-to-I Human chr15 + 40904400 40904400 40904400 CACAAGGTCAGGAGATCGAGACAATCCTGGCTAACACGATGAAACCCCGTCTCTCCTAAAAATAC CACAAGGTCAGGAGATCGAGACAATCCTGGCTGACACGATGAAACCCCGTCTCTCCTAAAAATAC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947119580 Functional Loss SNV dbSNP153 33..33 33 - - - 7799 RMVar_ID_7799 Human_SNP_ID_574578612 A-to-I Human chr15 + 40971945 40971945 40971945 CTCAGCCTCCCGAGTAGTTGGGAATTATAGGTATCCACCACCATGCCTGGCTAATTTTTGCGTTT CTCAGCCTCCCGAGTAGTTGGGAATTATAGGTGTCCACCACCATGCCTGGCTAATTTTTGCGTTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1387494543 Functional Loss SNV dbSNP153 33..33 33 - - - 7800 RMVar_ID_7800 Human_SNP_ID_574578618 A-to-I Human chr15 + 40971955 40971955 40971955 CGAGTAGTTGGGAATTATAGGTATCCACCACCATGCCTGGCTAATTTTTGCGTTTTTAGTGCAGA CGAGTAGTTGGGAATTATAGGTATCCACCACCCTGCCTGGCTAATTTTTGCGTTTTTAGTGCAGA A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054099839 Functional Loss SNV dbSNP153 33..33 33 - - - 7801 RMVar_ID_7801 Human_SNP_ID_574578628 A-to-I Human chr15 + 40972000 40972000 40972000 TTTTGCGTTTTTAGTGCAGACAGGGTTTCACCATGTTGACCAGGCTGGTCTCAAACTCCTGACCT TTTTGCGTTTTTAGTGCAGACAGGGTTTCACCGTGTTGACCAGGCTGGTCTCAAACTCCTGACCT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs770416923 Functional Loss SNV dbSNP153 33..33 33 - - - 7802 RMVar_ID_7802 Human_SNP_ID_574580107 A-to-I Human chr15 - 40975837 40975837 40975837 ACAGCTACACTGCCACAAATTGTCTGTGAGACAGGATTTTGCTCTGTCACCCAGGCTGGAGTGCA ACAGCTACACTGCCACAAATTGTCTGTGAGACGGGATTTTGCTCTGTCACCCAGGCTGGAGTGCA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1326068836 Functional Loss SNV dbSNP153 33..33 33 - - - 7803 RMVar_ID_7803 Human_SNP_ID_574583315 A-to-I Human chr15 - 40985864 40985864 40985864 TTGCTGTGTTGCCCAGACTGGAGTACAGTGTCACAATCCTGGCTCACCACAACCTCCACTTCCTG TTGCTGTGTTGCCCAGACTGGAGTACAGTGTCTCAATCCTGGCTCACCACAACCTCCACTTCCTG T A INO80 Ensembl:ENSG00000128908 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1385796901 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8438,RMVar_hsa_circ_92257,RMVar_hsa_circ_121224,RMVar_hsa_circ_170976,RMVar_hsa_circ_111223,RMVar_hsa_circ_170975,RMVar_hsa_circ_170977,RMVar_hsa_circ_90539,RMVar_hsa_circ_170978,RMVar_hsa_circ_298434,RMVar_hsa_circ_363812,RMVar_hsa_circ_170980,RMVar_hsa_circ_170981 7804 RMVar_ID_7804 Human_SNP_ID_574586299 A-to-I Human chr15 - 40997051 40997051 40997051 GCTGGTCTTGAACTCTGAGGCCCAAGTGATCCACCTGCCTCAGCCTCCCAAAGTACTGGGATTAC GCTGGTCTTGAACTCTGAGGCCCAAGTGATCCGCCTGCCTCAGCCTCCCAAAGTACTGGGATTAC T C INO80 Ensembl:ENSG00000128908 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947743222 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12500174 RMVar_hsa_circ_8438,RMVar_hsa_circ_92257,RMVar_hsa_circ_121224,RMVar_hsa_circ_170976,RMVar_hsa_circ_111223,RMVar_hsa_circ_170975,RMVar_hsa_circ_170977,RMVar_hsa_circ_90539,RMVar_hsa_circ_170978,RMVar_hsa_circ_170983,RMVar_hsa_circ_170981,RMVar_hsa_circ_89339,RMVar_hsa_circ_21238 7805 RMVar_ID_7805 Human_SNP_ID_574587254 A-to-I Human chr15 - 41000619 41000619 41000619 GCAATTAGAACTCACTGCATCCTTGACCTCCCAGGCTCTAGTGACTCTCCTACCTCAGCCTCCCA GCAATTAGAACTCACTGCATCCTTGACCTCCCGGGCTCTAGTGACTCTCCTACCTCAGCCTCCCA T C INO80 Ensembl:ENSG00000128908 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs370286537 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2439542,Human_RBP_ID_12500208 RMVar_hsa_circ_92257,RMVar_hsa_circ_121224,RMVar_hsa_circ_170976,RMVar_hsa_circ_111223,RMVar_hsa_circ_170975,RMVar_hsa_circ_170977,RMVar_hsa_circ_90539,RMVar_hsa_circ_170978,RMVar_hsa_circ_15350,RMVar_hsa_circ_170983,RMVar_hsa_circ_89339,RMVar_hsa_circ_265329,RMVar_hsa_circ_293692,RMVar_hsa_circ_32785,RMVar_hsa_circ_170984 7806 RMVar_ID_7806 Human_SNP_ID_574597265 A-to-I Human chr15 - 41039236 41039236 41039236 GTGTTGGCTCATGCCTTTAATCTCAGTACTTTAGGAGGCTGAGGTGGGAGGATTGCTTGGAGCCA GTGTTGGCTCATGCCTTTAATCTCAGTACTTTTGGAGGCTGAGGTGGGAGGATTGCTTGGAGCCA T A INO80 Ensembl:ENSG00000128908 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs889206822 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25185107 RMVar_hsa_circ_92257,RMVar_hsa_circ_121224,RMVar_hsa_circ_170976,RMVar_hsa_circ_111223,RMVar_hsa_circ_170975,RMVar_hsa_circ_170977,RMVar_hsa_circ_90539,RMVar_hsa_circ_170978,RMVar_hsa_circ_15350,RMVar_hsa_circ_170983,RMVar_hsa_circ_89339,RMVar_hsa_circ_265329,RMVar_hsa_circ_96852,RMVar_hsa_circ_170986,RMVar_hsa_circ_317056,RMVar_hsa_circ_118564,RMVar_hsa_circ_38200,RMVar_hsa_circ_170987,RMVar_hsa_circ_170988,RMVar_hsa_circ_334805,RMVar_hsa_circ_170990,RMVar_hsa_circ_170991,RMVar_hsa_circ_16209 7807 RMVar_ID_7807 Human_SNP_ID_574597275 A-to-I Human chr15 - 41039275 41039275 41039275 TAGAAATAGTATTGTTAAATTGGATCTAGGCCAGGTGTGGTGTTGGCTCATGCCTTTAATCTCAG TAGAAATAGTATTGTTAAATTGGATCTAGGCCGGGTGTGGTGTTGGCTCATGCCTTTAATCTCAG T C INO80 Ensembl:ENSG00000128908 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1384494836 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92257,RMVar_hsa_circ_121224,RMVar_hsa_circ_170976,RMVar_hsa_circ_111223,RMVar_hsa_circ_170975,RMVar_hsa_circ_170977,RMVar_hsa_circ_90539,RMVar_hsa_circ_170978,RMVar_hsa_circ_15350,RMVar_hsa_circ_170983,RMVar_hsa_circ_89339,RMVar_hsa_circ_265329,RMVar_hsa_circ_96852,RMVar_hsa_circ_170986,RMVar_hsa_circ_317056,RMVar_hsa_circ_118564,RMVar_hsa_circ_38200,RMVar_hsa_circ_170987,RMVar_hsa_circ_170988,RMVar_hsa_circ_334805,RMVar_hsa_circ_170990,RMVar_hsa_circ_170991,RMVar_hsa_circ_16209 7808 RMVar_ID_7808 Human_SNP_ID_574597582 A-to-I Human chr15 - 41040653 41040653 41040653 TTGTTCAGGCCGGCCTCGAACTCTGGCCTCAAACAATCCTCCGGCCTCAGCCTCCCAAAGTGCTG TTGTTCAGGCCGGCCTCGAACTCTGGCCTCAAGCAATCCTCCGGCCTCAGCCTCCCAAAGTGCTG T C INO80 Ensembl:ENSG00000128908 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1319236204 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92257,RMVar_hsa_circ_121224,RMVar_hsa_circ_170976,RMVar_hsa_circ_111223,RMVar_hsa_circ_170975,RMVar_hsa_circ_170977,RMVar_hsa_circ_90539,RMVar_hsa_circ_170978,RMVar_hsa_circ_15350,RMVar_hsa_circ_170983,RMVar_hsa_circ_89339,RMVar_hsa_circ_265329,RMVar_hsa_circ_96852,RMVar_hsa_circ_170986,RMVar_hsa_circ_317056,RMVar_hsa_circ_118564,RMVar_hsa_circ_38200,RMVar_hsa_circ_170987,RMVar_hsa_circ_170988,RMVar_hsa_circ_334805,RMVar_hsa_circ_170990,RMVar_hsa_circ_170991,RMVar_hsa_circ_16209 7809 RMVar_ID_7809 Human_SNP_ID_574605597 A-to-I Human chr15 - 41069375 41069375 41069375 ACGAGGTCAGGAAGTCGAGATCATCCTGGCTAACATGGTGAAACCCCGTCTCTACTAAAAATACA ACGAGGTCAGGAAGTCGAGATCATCCTGGCTAGCATGGTGAAACCCCGTCTCTACTAAAAATACA T C INO80 Ensembl:ENSG00000128908 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1354333815 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_599,RMVar_hsa_circ_92257,RMVar_hsa_circ_170978,RMVar_hsa_circ_15350,RMVar_hsa_circ_170983,RMVar_hsa_circ_89339,RMVar_hsa_circ_96852,RMVar_hsa_circ_170986,RMVar_hsa_circ_118564,RMVar_hsa_circ_170993,RMVar_hsa_circ_170988,RMVar_hsa_circ_340068,RMVar_hsa_circ_375539,RMVar_hsa_circ_362379,RMVar_hsa_circ_351258,RMVar_hsa_circ_337666,RMVar_hsa_circ_317916,RMVar_hsa_circ_170995,RMVar_hsa_circ_170994,RMVar_hsa_circ_60772,RMVar_hsa_circ_336402,RMVar_hsa_circ_371833,RMVar_hsa_circ_71454,RMVar_hsa_circ_171002,RMVar_hsa_circ_171003,RMVar_hsa_circ_265736,RMVar_hsa_circ_266111,RMVar_hsa_circ_333491,RMVar_hsa_circ_93473,RMVar_hsa_circ_348116,RMVar_hsa_circ_171004,RMVar_hsa_circ_10948,RMVar_hsa_circ_50094,RMVar_hsa_circ_70352,RMVar_hsa_circ_33455,RMVar_hsa_circ_326792,RMVar_hsa_circ_332302,RMVar_hsa_circ_310959,RMVar_hsa_circ_67698,RMVar_hsa_circ_46166,RMVar_hsa_circ_171011,RMVar_hsa_circ_16942,RMVar_hsa_circ_171012,RMVar_hsa_circ_171010,RMVar_hsa_circ_319185,RMVar_hsa_circ_378848,RMVar_hsa_circ_171015,RMVar_hsa_circ_171014,RMVar_hsa_circ_65314,RMVar_hsa_circ_276129 7810 RMVar_ID_7810 Human_SNP_ID_574607551 A-to-I Human chr15 - 41076249 41076249 41076249 TCAAGCGATTCTCCTGCTTCAGCCTCCTAAGTAGCTGGGATTACAGGCGCCTGCCACCATGCCTG TCAAGCGATTCTCCTGCTTCAGCCTCCTAAGTGGCTGGGATTACAGGCGCCTGCCACCATGCCTG T C INO80 Ensembl:ENSG00000128908 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1277280589 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92257,RMVar_hsa_circ_170978,RMVar_hsa_circ_15350,RMVar_hsa_circ_118564,RMVar_hsa_circ_170993,RMVar_hsa_circ_170988,RMVar_hsa_circ_340068,RMVar_hsa_circ_362379,RMVar_hsa_circ_337666,RMVar_hsa_circ_317916,RMVar_hsa_circ_336402,RMVar_hsa_circ_371833,RMVar_hsa_circ_71454,RMVar_hsa_circ_171002,RMVar_hsa_circ_171003,RMVar_hsa_circ_266111,RMVar_hsa_circ_333491,RMVar_hsa_circ_93473,RMVar_hsa_circ_171004,RMVar_hsa_circ_10948,RMVar_hsa_circ_70352,RMVar_hsa_circ_33455,RMVar_hsa_circ_326792,RMVar_hsa_circ_310959,RMVar_hsa_circ_46166,RMVar_hsa_circ_171011,RMVar_hsa_circ_171012,RMVar_hsa_circ_319185,RMVar_hsa_circ_115728,RMVar_hsa_circ_65314,RMVar_hsa_circ_299635,RMVar_hsa_circ_318821,RMVar_hsa_circ_331745,RMVar_hsa_circ_301825,RMVar_hsa_circ_271744,RMVar_hsa_circ_171020,RMVar_hsa_circ_171022,RMVar_hsa_circ_171024,RMVar_hsa_circ_171023,RMVar_hsa_circ_171021,RMVar_hsa_circ_28703,RMVar_hsa_circ_294282,RMVar_hsa_circ_369789,RMVar_hsa_circ_127897,RMVar_hsa_circ_171026,RMVar_hsa_circ_171027,RMVar_hsa_circ_171025,RMVar_hsa_circ_282540,RMVar_hsa_circ_54622,RMVar_hsa_circ_2069,RMVar_hsa_circ_59266,RMVar_hsa_circ_45288 7811 RMVar_ID_7811 Human_SNP_ID_574611138 A-to-I Human chr15 - 41089026 41089026 41089026 GCCACCATGCCTGGCTAATTTTTTTTATTTTTAGTAGAGATGTGGTTTCATCATGTTGGCCAGGC GCCACCATGCCTGGCTAATTTTTTTTATTTTTGGTAGAGATGTGGTTTCATCATGTTGGCCAGGC T C INO80 Ensembl:ENSG00000128908 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs953772701 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12501375 RMVar_hsa_circ_13904,RMVar_hsa_circ_92257,RMVar_hsa_circ_170978,RMVar_hsa_circ_15350,RMVar_hsa_circ_170993,RMVar_hsa_circ_340068,RMVar_hsa_circ_317916,RMVar_hsa_circ_371833,RMVar_hsa_circ_171003,RMVar_hsa_circ_333491,RMVar_hsa_circ_10948,RMVar_hsa_circ_326792,RMVar_hsa_circ_46166,RMVar_hsa_circ_115728,RMVar_hsa_circ_318821,RMVar_hsa_circ_331745,RMVar_hsa_circ_171024,RMVar_hsa_circ_171023,RMVar_hsa_circ_127897,RMVar_hsa_circ_171025,RMVar_hsa_circ_127167,RMVar_hsa_circ_54622,RMVar_hsa_circ_2069,RMVar_hsa_circ_349691,RMVar_hsa_circ_329363,RMVar_hsa_circ_171031,RMVar_hsa_circ_171032,RMVar_hsa_circ_171033,RMVar_hsa_circ_350399,RMVar_hsa_circ_352416,RMVar_hsa_circ_292211,RMVar_hsa_circ_74237,RMVar_hsa_circ_55716 7812 RMVar_ID_7812 Human_SNP_ID_574614616 A-to-I Human chr15 - 41101033 41101033 41101033 TTGATGCCAGGCGTTTGAGACCAGCCTGGCCAACATGGTAAAACTCCATCTCTACTAAAAATACA TTGATGCCAGGCGTTTGAGACCAGCCTGGCCATCATGGTAAAACTCCATCTCTACTAAAAATACA T A INO80 Ensembl:ENSG00000128908 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs974147219 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92257,RMVar_hsa_circ_170978,RMVar_hsa_circ_127897,RMVar_hsa_circ_171025,RMVar_hsa_circ_127167,RMVar_hsa_circ_171033 7813 RMVar_ID_7813 Human_SNP_ID_574615358 A-to-I Human chr15 - 41103972 41103972 41103972 ACCTCAGGTGATCAGCCTTCCTTGGCCTCCCAAGGTGCTGGGATTACAGGCGTGAGCCACTGCGC ACCTCAGGTGATCAGCCTTCCTTGGCCTCCCAGGGTGCTGGGATTACAGGCGTGAGCCACTGCGC T C INO80 Ensembl:ENSG00000128908 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1323514292 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92257,RMVar_hsa_circ_170978,RMVar_hsa_circ_127897,RMVar_hsa_circ_171025,RMVar_hsa_circ_127167,RMVar_hsa_circ_171033 7814 RMVar_ID_7814 Human_SNP_ID_574615385 A-to-I Human chr15 - 41104053 41104053 41104053 CCACACCTGACTAACTTTGTTGTATTTTTAGTAGAGACGAGGTTTCTCCATGTTGGTCAGATGGC CCACACCTGACTAACTTTGTTGTATTTTTAGTGGAGACGAGGTTTCTCCATGTTGGTCAGATGGC T C INO80 Ensembl:ENSG00000128908 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1045131506 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92257,RMVar_hsa_circ_170978,RMVar_hsa_circ_127897,RMVar_hsa_circ_171025,RMVar_hsa_circ_127167,RMVar_hsa_circ_171033 7815 RMVar_ID_7815 Human_SNP_ID_574617161 A-to-I Human chr15 - 41110283 41110283 41110283 AAAATTGGGTGAGTGTGCTGGCACGTGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGTAGA AAAATTGGGTGAGTGTGCTGGCACGTGCCTGTGGTCCCAGCTACTTGGGAGGCTGAGGCAGTAGA T C INO80 Ensembl:ENSG00000128908 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs564126391 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92257,RMVar_hsa_circ_170978,RMVar_hsa_circ_127897,RMVar_hsa_circ_171025,RMVar_hsa_circ_127167,RMVar_hsa_circ_171033 7816 RMVar_ID_7816 Human_SNP_ID_574617812 A-to-I Human chr15 - 41112705 41112705 41112705 AGGCTCACTGCACCCTCTGCCTCCCGGGTTCAAGAAATTCTCCTGCTTCATTCTCCCAAGTAGCT AGGCTCACTGCACCCTCTGCCTCCCGGGTTCAGGAAATTCTCCTGCTTCATTCTCCCAAGTAGCT T C INO80 Ensembl:ENSG00000128908 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs944489343 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12501661 RMVar_hsa_circ_92257,RMVar_hsa_circ_170978,RMVar_hsa_circ_127897,RMVar_hsa_circ_171025,RMVar_hsa_circ_127167,RMVar_hsa_circ_171033 7817 RMVar_ID_7817 Human_SNP_ID_574617965 A-to-I Human chr15 - 41113008 41113008 41113008 GGGATGCTGAGGTGAGAGGATGGCTTGAGCCCAGGAGGCAGAGATTGCAGTGAGCCGAGATCGAG GGGATGCTGAGGTGAGAGGATGGCTTGAGCCCGGGAGGCAGAGATTGCAGTGAGCCGAGATCGAG T C INO80 Ensembl:ENSG00000128908 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1174068600 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92257,RMVar_hsa_circ_170978,RMVar_hsa_circ_127897,RMVar_hsa_circ_171025,RMVar_hsa_circ_127167,RMVar_hsa_circ_171033 7818 RMVar_ID_7818 Human_SNP_ID_574631458 A-to-I Human chr15 - 41163832 41163832 41163832 TAATTGCTTAGCTTCTCGATTCCTTGCTGTGAATGTTGCTTTGAGGTCATCCCGTTTCATTTTCA TAATTGCTTAGCTTCTCGATTCCTTGCTGTGAGTGTTGCTTTGAGGTCATCCCGTTTCATTTTCA T C lnc-EXD1-1 RNACentral:URS00008BD8C6 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1408544419 Functional Loss SNV dbSNP153 33..33 33 - - - 7819 RMVar_ID_7819 Human_SNP_ID_574650761 A-to-I Human chr15 + 41234089 41234089 41234089 CTCCCGCTTCAGCGTCCCAAGTAGCTAGGACTACAGGCGCATACCACCATGCTTACCTGATTTTT CTCCCGCTTCAGCGTCCCAAGTAGCTAGGACTGCAGGCGCATACCACCATGCTTACCTGATTTTT A G CHP1 Ensembl:ENSG00000187446 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1377626448 Functional Loss SNV dbSNP153 33..33 33 - - - 7820 RMVar_ID_7820 Human_SNP_ID_574651938 A-to-I Human chr15 + 41238801 41238801 41238801 CTGAACCTGGGAGGCAGAGTTTGCAGTGAGCCAAGATCGCGCCACTGCACTCCATCCTGGGTGAC CTGAACCTGGGAGGCAGAGTTTGCAGTGAGCCGAGATCGCGCCACTGCACTCCATCCTGGGTGAC A G CHP1 Ensembl:ENSG00000187446 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1409763216 Functional Loss SNV dbSNP153 33..33 33 - - - 7821 RMVar_ID_7821 Human_SNP_ID_574656788 A-to-I Human chr15 + 41257677 41257677 41257677 TGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCGAGATAGTTGGGATTACAGCCACATG TGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCCGCCTCCGAGATAGTTGGGATTACAGCCACATG A C CHP1 Ensembl:ENSG00000187446 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs546587632 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_291411,RMVar_hsa_circ_340146,RMVar_hsa_circ_294318,RMVar_hsa_circ_171038,RMVar_hsa_circ_171040,RMVar_hsa_circ_278288,RMVar_hsa_circ_171039,RMVar_hsa_circ_48808,RMVar_hsa_circ_293038,RMVar_hsa_circ_288109,RMVar_hsa_circ_171041,RMVar_hsa_circ_9883 7822 RMVar_ID_7822 Human_SNP_ID_574662688 A-to-I Human chr15 + 41280988 41280988 41280988 TCAAGCAATTCTCCCACCTCAGCCTCCCAAGTAGCTGGGATTACAGACGTGTGCCACCATACCTG TCAAGCAATTCTCCCACCTCAGCCTCCCAAGTGGCTGGGATTACAGACGTGTGCCACCATACCTG A G CHP1 Ensembl:ENSG00000187446 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1383823809 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116348,RMVar_hsa_circ_121813,RMVar_hsa_circ_171042,RMVar_hsa_circ_171043 7823 RMVar_ID_7823 Human_SNP_ID_574662700 A-to-I Human chr15 + 41281024 41281024 41281024 GGGATTACAGACGTGTGCCACCATACCTGGGTAATTTTTGCATTTTTAGTGGAGAGGGAGTTTCA GGGATTACAGACGTGTGCCACCATACCTGGGTGATTTTTGCATTTTTAGTGGAGAGGGAGTTTCA A G CHP1 Ensembl:ENSG00000187446 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1343295049 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6423690,Human_RBP_ID_12653921,Human_RBP_ID_17249731,Human_RBP_ID_20019751,Human_RBP_ID_26433656 RMVar_hsa_circ_116348,RMVar_hsa_circ_121813,RMVar_hsa_circ_171042,RMVar_hsa_circ_171043 7824 RMVar_ID_7824 Human_SNP_ID_574664426 A-to-I Human chr15 + 41287715 41287715 41287715 GGGCGCGGTGGCTCATGCCTGTAATCCTGGCTACTCAGGAGGCTGTGGCAGGAGTATCGCTTGAA GGGCGCGGTGGCTCATGCCTGTAATCCTGGCTCCTCAGGAGGCTGTGGCAGGAGTATCGCTTGAA A C OIP5-AS1,AC087721.2 Ensembl:ENSG00000247556,Ensembl:ENSG00000285920 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1463392263 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8251459,Human_RBP_ID_12502127 RMVar_hsa_circ_121853,RMVar_hsa_circ_171044 7825 RMVar_ID_7825 Human_SNP_ID_574664593 A-to-I Human chr15 + 41288188 41288188 41288188 TTGAACTCCTGACCTCGTGATCCGCCCACCTTAGCCTCCCAAAATGCTGAGATTGGAGGTGTGAG TTGAACTCCTGACCTCGTGATCCGCCCACCTTGGCCTCCCAAAATGCTGAGATTGGAGGTGTGAG A G OIP5-AS1,AC087721.2 Ensembl:ENSG00000247556,Ensembl:ENSG00000285920 lincRNA,Protein coding intron,intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1269491052 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121853,RMVar_hsa_circ_171044 7826 RMVar_ID_7826 Human_SNP_ID_574664597 A-to-I Human chr15 + 41288197 41288197 41288197 TGACCTCGTGATCCGCCCACCTTAGCCTCCCAAAATGCTGAGATTGGAGGTGTGAGCCACCGCGC TGACCTCGTGATCCGCCCACCTTAGCCTCCCACAATGCTGAGATTGGAGGTGTGAGCCACCGCGC A C OIP5-AS1,AC087721.2 Ensembl:ENSG00000247556,Ensembl:ENSG00000285920 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1260171509 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3490403,Human_RBP_ID_12502138 RMVar_hsa_circ_121853,RMVar_hsa_circ_171044 7827 RMVar_ID_7827 Human_SNP_ID_574664902 A-to-I Human chr15 + 41289502 41289502 41289502 CCTGGCCAACATGGTGAAACTGTGTCTTTACTAAAAATACAAAAATTAGTCGGGCATAGTGGTAA CCTGGCCAACATGGTGAAACTGTGTCTTTACTGAAAATACAAAAATTAGTCGGGCATAGTGGTAA A G OIP5-AS1,AC087721.2 Ensembl:ENSG00000247556,Ensembl:ENSG00000285920 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs922411367 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2439766,Human_RBP_ID_3490410 RMVar_hsa_circ_121853,RMVar_hsa_circ_171044 7828 RMVar_ID_7828 Human_SNP_ID_574666407 A-to-I Human chr15 + 41293936 41293936 41293936 CAGGTTGGAATGCAGTGGTGCGATCTCGTCTCACTGCAACGTCTGCCCCTCGGACTCAAGTTGTC CAGGTTGGAATGCAGTGGTGCGATCTCGTCTCTCTGCAACGTCTGCCCCTCGGACTCAAGTTGTC A T OIP5-AS1,AC087721.2 Ensembl:ENSG00000247556,Ensembl:ENSG00000285920 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904938825 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3490412,Human_RBP_ID_5247225,Human_RBP_ID_12502326 RMVar_hsa_circ_121853,RMVar_hsa_circ_171044 7829 RMVar_ID_7829 Human_SNP_ID_574666629 A-to-I Human chr15 + 41294895 41294895 41294895 TTTCAGTTTTTGTAGAGACAGAATGTCAGTATATTGCCAGGCTAGTCTCGAACTCGTGAGCTCAA TTTCAGTTTTTGTAGAGACAGAATGTCAGTATGTTGCCAGGCTAGTCTCGAACTCGTGAGCTCAA A G OIP5-AS1,AC087721.2 Ensembl:ENSG00000247556,Ensembl:ENSG00000285920 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1372929499 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12502352,Human_RBP_ID_22579170 RMVar_hsa_circ_121853,RMVar_hsa_circ_171044 7830 RMVar_ID_7830 Human_SNP_ID_574667111 A-to-I Human chr15 + 41296847 41296847 41296847 GAAGATGCAGTGCTACCTTATTTTTCATTTTTATTTTTTGGAGACAGAGTCTCACTCTGTTGCCC GAAGATGCAGTGCTACCTTATTTTTCATTTTTTTTTTTTGGAGACAGAGTCTCACTCTGTTGCCC A T OIP5-AS1,AC087721.2 Ensembl:ENSG00000247556,Ensembl:ENSG00000285920 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs963711820 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6423765,Human_RBP_ID_12502431,Human_RBP_ID_25183292 Human_Splice_Rec_1586382 RMVar_hsa_circ_121853,RMVar_hsa_circ_171044 7831 RMVar_ID_7831 Human_SNP_ID_574667342 A-to-I Human chr15 + 41297671 41297663 41297671 TTCTTTTTTTTGTTTGTTTGTTTGTTTGTTTGAGACGGAGTCACGTTCTGTTGCCTGGGCTGGAG TTCTTTTTTTTGTTTGTTTGTTTGT________GACGGAGTCACGTTCTGTTGCCTGGGCTGGAG TTTGTTTGA T OIP5-AS1,AC087721.2 Ensembl:ENSG00000247556,Ensembl:ENSG00000285920 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1326021149 Functional Loss DEL dbSNP153 26..33 33 - - - Human_RBP_ID_6423770,Human_RBP_ID_12502441,Human_RBP_ID_23650766 RMVar_hsa_circ_121853,RMVar_hsa_circ_171044 7832 RMVar_ID_7832 Human_SNP_ID_574667395 A-to-I Human chr15 + 41297832 41297832 41297832 CGTTACCACGCCCAGCTAATTTTTGTATCTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGC CGTTACCACGCCCAGCTAATTTTTGTATCTTTGGTAGAGACGGGGTTTCACCATGTTGGCCAGGC A G OIP5-AS1,AC087721.2 Ensembl:ENSG00000247556,Ensembl:ENSG00000285920 lincRNA,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1278285317 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121853,RMVar_hsa_circ_171044 7833 RMVar_ID_7833 Human_SNP_ID_574667564 A-to-I Human chr15 + 41298725 41298725 41298725 TGAGACCAGCCTGACCAACATGGAGAAACCCCATCTCTACTAAAAATAGAAAATTAGCCAGGTGT TGAGACCAGCCTGACCAACATGGAGAAACCCCGTCTCTACTAAAAATAGAAAATTAGCCAGGTGT A G OIP5-AS1,AC087721.2 Ensembl:ENSG00000247556,Ensembl:ENSG00000285920 lincRNA,Protein coding exon,intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1465844142 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6485515,Human_RBP_ID_23161507 RMVar_hsa_circ_121853,RMVar_hsa_circ_171044 7834 RMVar_ID_7834 Human_SNP_ID_574667570 A-to-I Human chr15 + 41298748 41298748 41298748 AGAAACCCCATCTCTACTAAAAATAGAAAATTAGCCAGGTGTGGTGGTAGATACGTGTAATCCCA AGAAACCCCATCTCTACTAAAAATAGAAAATTTGCCAGGTGTGGTGGTAGATACGTGTAATCCCA A T OIP5-AS1,AC087721.2 Ensembl:ENSG00000247556,Ensembl:ENSG00000285920 lincRNA,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1402324499 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121853,RMVar_hsa_circ_171044 7835 RMVar_ID_7835 Human_SNP_ID_574667689 A-to-I Human chr15 + 41299136 41299136 41299136 TGGATGTTTGATTTTTATTTATTTATTTATTTATTTTTTGAGGCAGTCTCTCTCTGTTGCCCAGG TGGATGTTTGATTTTTATTTATTTATTTATTTTTTTTTTGAGGCAGTCTCTCTCTGTTGCCCAGG A T OIP5-AS1,AC087721.2 Ensembl:ENSG00000247556,Ensembl:ENSG00000285920 lincRNA,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1440262750 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2439784,Human_RBP_ID_3473779,Human_RBP_ID_4320475,Human_RBP_ID_6423783,Human_RBP_ID_8416176,Human_RBP_ID_12502465,Human_RBP_ID_23161510,Human_RBP_ID_24473406 Human_miRNA_ID_3086425,Human_miRNA_ID_3214288 RMVar_hsa_circ_121853,RMVar_hsa_circ_171044 7836 RMVar_ID_7836 Human_SNP_ID_574667722 A-to-I Human chr15 + 41299253 41299253 41299253 GCGATTCTCCTGCCTCAGCCTCCCAAGTAGCTAGGATTACAGGCGCGCACCACCACGCTCAGCCT GCGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCGCGCACCACCACGCTCAGCCT A G OIP5-AS1,AC087721.2 Ensembl:ENSG00000247556,Ensembl:ENSG00000285920 lincRNA,Protein coding exon,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs3210775 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17859873,Human_RBP_ID_27434893 RMVar_hsa_circ_121853,RMVar_hsa_circ_171044 7837 RMVar_ID_7837 Human_SNP_ID_574668159 A-to-I Human chr15 + 41301045 41301045 41301045 CAGGCTGGAGTGCAGTGGCACAATCTTTGCTCACTGTAACCTCTGCCTCTTGGGTTCAAGTGATT CAGGCTGGAGTGCAGTGGCACAATCTTTGCTCTCTGTAACCTCTGCCTCTTGGGTTCAAGTGATT A T OIP5-AS1,AC087721.2 Ensembl:ENSG00000247556,Ensembl:ENSG00000285920 lincRNA,Protein coding exon,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs918273035 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_456899,Human_RBP_ID_8799483 Human_miRNA_ID_3165740 7838 RMVar_ID_7838 Human_SNP_ID_574668491 A-to-I Human chr15 + 41302238 41302238 41302238 TGCACAAGGGCCAGGTGCGGTGGCTTACACCTATAATCCCAGCACTTTGGGAGGCCAAGGTGGGC TGCACAAGGGCCAGGTGCGGTGGCTTACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGC A G OIP5-AS1,AC087721.2 Ensembl:ENSG00000247556,Ensembl:ENSG00000285920 lincRNA,Protein coding exon,intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs1008105422 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8183619 7839 RMVar_ID_7839 Human_SNP_ID_574668522 A-to-I Human chr15 + 41302363 41302363 41302363 TAAAAATACAAAACTTAGCTGGGCATGGTGGCACATGCCTGTAATCCCAGCTACTCAGGAGGCTG TAAAAATACAAAACTTAGCTGGGCATGGTGGCCCATGCCTGTAATCCCAGCTACTCAGGAGGCTG A C OIP5-AS1,AC087721.2 Ensembl:ENSG00000247556,Ensembl:ENSG00000285920 lincRNA,Protein coding exon,intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1567020994 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25136897 7840 RMVar_ID_7840 Human_SNP_ID_574668529 A-to-I Human chr15 + 41302383 41302383 41302383 GGGCATGGTGGCACATGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGTAGAATCACTTAAA GGGCATGGTGGCACATGCCTGTAATCCCAGCTGCTCAGGAGGCTGAGGCAGTAGAATCACTTAAA A G OIP5-AS1,AC087721.2 Ensembl:ENSG00000247556,Ensembl:ENSG00000285920 lincRNA,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1243881537 Functional Loss SNV dbSNP153 33..33 33 - - - 7841 RMVar_ID_7841 Human_SNP_ID_574668530 A-to-I Human chr15 + 41302387 41302387 41302387 ATGGTGGCACATGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGTAGAATCACTTAAACCTG ATGGTGGCACATGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGTAGAATCACTTAAACCTG A G OIP5-AS1,AC087721.2 Ensembl:ENSG00000247556,Ensembl:ENSG00000285920 lincRNA,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1322115123 Functional Loss SNV dbSNP153 33..33 33 - - - 7842 RMVar_ID_7842 Human_SNP_ID_574668542 A-to-I Human chr15 + 41302454 41302454 41302454 AGGCGGAGGTTGCAGTGAGCTGAGATCACACCACTGTACTCCAGCCTGGTGACAGTAAGACTCCA AGGCGGAGGTTGCAGTGAGCTGAGATCACACCGCTGTACTCCAGCCTGGTGACAGTAAGACTCCA A G OIP5-AS1,AC087721.2 Ensembl:ENSG00000247556,Ensembl:ENSG00000285920 lincRNA,Protein coding exon,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1157510430 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_456936,Human_RBP_ID_5646587,Human_RBP_ID_12502581 7843 RMVar_ID_7843 Human_SNP_ID_574669262 A-to-I Human chr15 + 41305325 41305325 41305325 TCTCAGCTCACTGCAACCTCCACCTCCCGAGTAGCTGGGATTACAGACATGCACCACCACCCTCA TCTCAGCTCACTGCAACCTCCACCTCCCGAGTGGCTGGGATTACAGACATGCACCACCACCCTCA A G OIP5-AS1,AC087721.2 Ensembl:ENSG00000247556,Ensembl:ENSG00000285920 lincRNA,Protein coding exon,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1192966318 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_3207751 7844 RMVar_ID_7844 Human_SNP_ID_574669265 A-to-I Human chr15 + 41305335 41305335 41305335 CTGCAACCTCCACCTCCCGAGTAGCTGGGATTACAGACATGCACCACCACCCTCAGCTAATTTTT CTGCAACCTCCACCTCCCGAGTAGCTGGGATTGCAGACATGCACCACCACCCTCAGCTAATTTTT A G OIP5-AS1,AC087721.2 Ensembl:ENSG00000247556,Ensembl:ENSG00000285920 lincRNA,Protein coding exon,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1433814507 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_3207751 7845 RMVar_ID_7845 Human_SNP_ID_574669275 A-to-I Human chr15 + 41305361 41305360 41305361 GGGATTACAGACATGCACCACCACCCTCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCG GGGATTACAGACATGCACCACCACCCTCAGCT_ATTTTTGTATTTTTAGTAGAGACGGGGTTTCG TA T OIP5-AS1,AC087721.2 Ensembl:ENSG00000247556,Ensembl:ENSG00000285920 lincRNA,Protein coding exon,intron GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-Seq:(High) rs1302840714 Functional Loss DEL dbSNP153 33..33 33 - - - 7846 RMVar_ID_7846 Human_SNP_ID_574669277 A-to-I Human chr15 + 41305361 41305361 41305361 GGGATTACAGACATGCACCACCACCCTCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCG GGGATTACAGACATGCACCACCACCCTCAGCTGATTTTTGTATTTTTAGTAGAGACGGGGTTTCG A G OIP5-AS1,AC087721.2 Ensembl:ENSG00000247556,Ensembl:ENSG00000285920 lincRNA,Protein coding exon,intron GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-Seq:(High) rs1380165304 Functional Loss SNV dbSNP153 33..33 33 - - - 7847 RMVar_ID_7847 Human_SNP_ID_574669281 A-to-I Human chr15 + 41305370 41305370 41305370 GACATGCACCACCACCCTCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCGCCATGTTGG GACATGCACCACCACCCTCAGCTAATTTTTGTGTTTTTAGTAGAGACGGGGTTTCGCCATGTTGG A G OIP5-AS1,AC087721.2 Ensembl:ENSG00000247556,Ensembl:ENSG00000285920 lincRNA,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1373443769 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_125443 7848 RMVar_ID_7848 Human_SNP_ID_574669284 A-to-I Human chr15 + 41305379 41305379 41305379 CACCACCCTCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCGCCATGTTGGCCAGGCTGG CACCACCCTCAGCTAATTTTTGTATTTTTAGTGGAGACGGGGTTTCGCCATGTTGGCCAGGCTGG A G OIP5-AS1,AC087721.2 Ensembl:ENSG00000247556,Ensembl:ENSG00000285920 lincRNA,Protein coding exon,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1132641 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6485545 7849 RMVar_ID_7849 Human_SNP_ID_574669319 A-to-I Human chr15 + 41305449 41305449 41305449 AACTCCTGGCCTTACGTGATCCGCCCCCCCTTAGCCTTCCAAAGTGCTGGGATTACAGGTGTGAG AACTCCTGGCCTTACGTGATCCGCCCCCCCTTGGCCTTCCAAAGTGCTGGGATTACAGGTGTGAG A G OIP5-AS1,AC087721.2 Ensembl:ENSG00000247556,Ensembl:ENSG00000285920 lincRNA,Protein coding exon,intron GSE38233;GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,30559470,31158229,31158229,31158229 RNA-Seq:(High) rs1350713502 Functional Loss SNV dbSNP153 33..33 33 - - - 7850 RMVar_ID_7850 Human_SNP_ID_574669320 A-to-I Human chr15 + 41305457 41305457 41305457 GCCTTACGTGATCCGCCCCCCCTTAGCCTTCCAAAGTGCTGGGATTACAGGTGTGAGCCACTGCA GCCTTACGTGATCCGCCCCCCCTTAGCCTTCCGAAGTGCTGGGATTACAGGTGTGAGCCACTGCA A G OIP5-AS1,AC087721.2 Ensembl:ENSG00000247556,Ensembl:ENSG00000285920 lincRNA,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1258209276 Functional Loss SNV dbSNP153 33..33 33 - - - 7851 RMVar_ID_7851 Human_SNP_ID_574669321 A-to-I Human chr15 + 41305458 41305458 41305458 CCTTACGTGATCCGCCCCCCCTTAGCCTTCCAAAGTGCTGGGATTACAGGTGTGAGCCACTGCAC CCTTACGTGATCCGCCCCCCCTTAGCCTTCCAGAGTGCTGGGATTACAGGTGTGAGCCACTGCAC A G OIP5-AS1,AC087721.2 Ensembl:ENSG00000247556,Ensembl:ENSG00000285920 lincRNA,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs796082497 Functional Loss SNV dbSNP153 33..33 33 - - - 7852 RMVar_ID_7852 Human_SNP_ID_574669962 A-to-I Human chr15 - 41307977 41307977 41307977 TTATGCTTTTTTTGAGGGGAGGGTGGTGAGACAGGGTCTCACTCTGTCACCCAGGCCTGAGTGCA TTATGCTTTTTTTGAGGGGAGGGTGGTGAGACGGGGTCTCACTCTGTCACCCAGGCCTGAGTGCA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs915154988 Functional Loss SNV dbSNP153 33..33 33 - - - 7853 RMVar_ID_7853 Human_SNP_ID_574670210 A-to-I Human chr15 + 41308838 41308838 41308838 CTTCTGCCTCAGGTTCCTGAGTAGCTGGGATTACAGGTGCGCACCACCATGCCTGGCTAATTTTT CTTCTGCCTCAGGTTCCTGAGTAGCTGGGATTGCAGGTGCGCACCACCATGCCTGGCTAATTTTT A G OIP5-AS1,AC087721.2 Ensembl:ENSG00000247556,Ensembl:ENSG00000285920 lincRNA,Protein coding exon,exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1026308277 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1586427 7854 RMVar_ID_7854 Human_SNP_ID_574670818 A-to-I Human chr15 + 41311623 41311623 41311623 ATAGATTCTCACTGTCACCCAGGCTAGAATGCAATGGCGTGATCTTGGCTCACTGCAACCTCTGC ATAGATTCTCACTGTCACCCAGGCTAGAATGCTATGGCGTGATCTTGGCTCACTGCAACCTCTGC A T AC087721.2 Ensembl:ENSG00000285920 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1325008250 Functional Loss SNV dbSNP153 33..33 33 - - - 7855 RMVar_ID_7855 Human_SNP_ID_574671205 A-to-I Human chr15 - 41312829 41312829 41312829 GGTCAGGAGATGGAGACCATCCTGGCTAACACAGTGAAACCCCATCTCTATTACAAATACAAAAA GGTCAGGAGATGGAGACCATCCTGGCTAACACCGTGAAACCCCATCTCTATTACAAATACAAAAA T G OIP5 Ensembl:ENSG00000104147 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs771325557 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104612,RMVar_hsa_circ_171048,RMVar_hsa_circ_95181,RMVar_hsa_circ_171047 7856 RMVar_ID_7856 Human_SNP_ID_574671846 A-to-I Human chr15 - 41315353 41315353 41315353 GTGATCTCAGCTCATTGCAACCTCCGCCTCCCAGGTTCAAGTGATTCTCCTGCCTTGCCTCCCAA GTGATCTCAGCTCATTGCAACCTCCGCCTCCCGGGTTCAAGTGATTCTCCTGCCTTGCCTCCCAA T C OIP5 Ensembl:ENSG00000104147 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1349672198 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_171048,RMVar_hsa_circ_95181,RMVar_hsa_circ_321186 7857 RMVar_ID_7857 Human_SNP_ID_574673909 A-to-I Human chr15 - 41322217 41322217 41322217 CTAGGCTGCTCTCGAATTCCTGGGCTCAAGCTATCTGCCCACTTTGGCCTCTCATAGTGCTGGGA CTAGGCTGCTCTCGAATTCCTGGGCTCAAGCTGTCTGCCCACTTTGGCCTCTCATAGTGCTGGGA T C OIP5 Ensembl:ENSG00000104147 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs895071335 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_171048,RMVar_hsa_circ_95181 7858 RMVar_ID_7858 Human_SNP_ID_574673910 A-to-I Human chr15 - 41322217 41322217 41322217 CTAGGCTGCTCTCGAATTCCTGGGCTCAAGCTATCTGCCCACTTTGGCCTCTCATAGTGCTGGGA CTAGGCTGCTCTCGAATTCCTGGGCTCAAGCTCTCTGCCCACTTTGGCCTCTCATAGTGCTGGGA T G OIP5 Ensembl:ENSG00000104147 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs895071335 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_171048,RMVar_hsa_circ_95181 7859 RMVar_ID_7859 Human_SNP_ID_574676498 A-to-I Human chr15 - 41331577 41331577 41331577 CAATCCTTTTAGATATTAGAACTTTTTGATACAGGGTCTTGCTCTCGCCCAGGCTGGAGTGCACT CAATCCTTTTAGATATTAGAACTTTTTGATACGGGGTCTTGCTCTCGCCCAGGCTGGAGTGCACT T C OIP5 Ensembl:ENSG00000104147 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1435638633 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6423990,Human_RBP_ID_12502970 RMVar_hsa_circ_171048,RMVar_hsa_circ_95181 7860 RMVar_ID_7860 Human_SNP_ID_574677609 A-to-I Human chr15 + 41334737 41334737 41334737 TGTGTGTGTGTGTGTGTATTTTTAGTAGAGATAGGGTTTCACCATCTTGCCCAGGCTGGTCTTGA TGTGTGTGTGTGTGTGTATTTTTAGTAGAGATGGGGTTTCACCATCTTGCCCAGGCTGGTCTTGA A G NUSAP1,AC087721.2 Ensembl:ENSG00000137804,Ensembl:ENSG00000285920 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1230686771 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99120,RMVar_hsa_circ_171049 7861 RMVar_ID_7861 Human_SNP_ID_574678654 A-to-I Human chr15 + 41338072 41338070 41338072 CTCCTGCCTCAGCCACCCGAGTTCCTGGGATTATAGGTGCCTGCCACCATGCCCAGCTAATTTTT CTCCTGCCTCAGCCACCCGAGTTCCTGGGAT__TAGGTGCCTGCCACCATGCCCAGCTAATTTTT TTA T NUSAP1,AC087721.2 Ensembl:ENSG00000137804,Ensembl:ENSG00000285920 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1489444174 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_99120,RMVar_hsa_circ_171049 7862 RMVar_ID_7862 Human_SNP_ID_574680184 A-to-I Human chr15 + 41344198 41344198 41344198 ATCAAACCATTGCACTCCACCCTGGGAGACAGAATGAGACTCCATCTCAAAAAAAAAAAAAAAAA ATCAAACCATTGCACTCCACCCTGGGAGACAGGATGAGACTCCATCTCAAAAAAAAAAAAAAAAA A G AC087721.1,NUSAP1,AC087721.2 Ensembl:ENSG00000259396,Ensembl:ENSG00000137804,Ensembl:ENSG00000285920 lincRNA,Protein coding,Protein coding exon,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1278555304 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1586706 RMVar_hsa_circ_5714,RMVar_hsa_circ_99120,RMVar_hsa_circ_66562,RMVar_hsa_circ_304812,RMVar_hsa_circ_171049,RMVar_hsa_circ_68859,RMVar_hsa_circ_64721 7863 RMVar_ID_7863 Human_SNP_ID_574680470 A-to-I Human chr15 + 41345165 41345165 41345165 GGGACTACAGCCTTGTATCACCATTCCTGGCTATTTTTTGTATTTTTAGTAGAGACGGGGTTTCA GGGACTACAGCCTTGTATCACCATTCCTGGCTGTTTTTTGTATTTTTAGTAGAGACGGGGTTTCA A G NUSAP1,AC087721.2 Ensembl:ENSG00000137804,Ensembl:ENSG00000285920 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs183691838 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12503124 RMVar_hsa_circ_5714,RMVar_hsa_circ_99120,RMVar_hsa_circ_66562,RMVar_hsa_circ_304812,RMVar_hsa_circ_171049,RMVar_hsa_circ_68859,RMVar_hsa_circ_64721 7864 RMVar_ID_7864 Human_SNP_ID_574680481 A-to-I Human chr15 + 41345220 41345220 41345220 CGGGGTTTCACAATATTGCCCGGGCTGGTCTCAAACTCCTGGGCTCAAGTAGTTTGCCTACCTCT CGGGGTTTCACAATATTGCCCGGGCTGGTCTCTAACTCCTGGGCTCAAGTAGTTTGCCTACCTCT A T NUSAP1,AC087721.2 Ensembl:ENSG00000137804,Ensembl:ENSG00000285920 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs920828594 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5714,RMVar_hsa_circ_99120,RMVar_hsa_circ_66562,RMVar_hsa_circ_304812,RMVar_hsa_circ_171049,RMVar_hsa_circ_68859,RMVar_hsa_circ_64721 7865 RMVar_ID_7865 Human_SNP_ID_574680702 A-to-I Human chr15 + 41346080 41346080 41346080 GAGATGGAGTCTTGCCCTGAGTAACTGGGATTACAGATGCACACCACCATGCCCAGCTAATTTTT GAGATGGAGTCTTGCCCTGAGTAACTGGGATTGCAGATGCACACCACCATGCCCAGCTAATTTTT A G NUSAP1,AC087721.2 Ensembl:ENSG00000137804,Ensembl:ENSG00000285920 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1355829710 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5714,RMVar_hsa_circ_99120,RMVar_hsa_circ_66562,RMVar_hsa_circ_304812,RMVar_hsa_circ_171049,RMVar_hsa_circ_68859,RMVar_hsa_circ_64721 7866 RMVar_ID_7866 Human_SNP_ID_574681103 A-to-I Human chr15 + 41347598 41347598 41347598 AGCACTTTGGGAGGCTGAGGTGGGCGGATCACAAGGTCAACAGATCGAGACCATCCTGGCTAACA AGCACTTTGGGAGGCTGAGGTGGGCGGATCACCAGGTCAACAGATCGAGACCATCCTGGCTAACA A C NUSAP1,AC087721.2 Ensembl:ENSG00000137804,Ensembl:ENSG00000285920 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1041292772 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5714,RMVar_hsa_circ_99120,RMVar_hsa_circ_66562,RMVar_hsa_circ_304812,RMVar_hsa_circ_171049,RMVar_hsa_circ_68859,RMVar_hsa_circ_64721 7867 RMVar_ID_7867 Human_SNP_ID_574682433 A-to-I Human chr15 + 41353174 41353173 41353175 TATCCTTTCTTTGTTTTGTTTTGTTTTGAGACAGAGTCTCTCTCTGTTGCCCAGGCGGGAGTACA TATCCTTTCTTTGTTTTGTTTTGTTTTGAGAC__AGTCTCTCTCTGTTGCCCAGGCGGGAGTACA CAG C NUSAP1,AC087721.2 Ensembl:ENSG00000137804,Ensembl:ENSG00000285920 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs563001631 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_99120,RMVar_hsa_circ_66562,RMVar_hsa_circ_171049,RMVar_hsa_circ_68859,RMVar_hsa_circ_64721,RMVar_hsa_circ_58522,RMVar_hsa_circ_26884,RMVar_hsa_circ_303269,RMVar_hsa_circ_335592,RMVar_hsa_circ_36821,RMVar_hsa_circ_355511,RMVar_hsa_circ_55546,RMVar_hsa_circ_74842,RMVar_hsa_circ_171051 7868 RMVar_ID_7868 Human_SNP_ID_574682897 A-to-I Human chr15 + 41355039 41355039 41355039 GAGACTCCATCTCAAAAAAAAAAAATAGAGACAGAGTCTTGCTGTGTTGCCCAGGCTCGTCTCAA GAGACTCCATCTCAAAAAAAAAAAATAGAGACGGAGTCTTGCTGTGTTGCCCAGGCTCGTCTCAA A G NUSAP1,AC087721.2 Ensembl:ENSG00000137804,Ensembl:ENSG00000285920 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1297818080 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99120,RMVar_hsa_circ_66562,RMVar_hsa_circ_171049,RMVar_hsa_circ_68859,RMVar_hsa_circ_64721,RMVar_hsa_circ_58522,RMVar_hsa_circ_26884,RMVar_hsa_circ_303269,RMVar_hsa_circ_335592,RMVar_hsa_circ_36821,RMVar_hsa_circ_355511,RMVar_hsa_circ_55546,RMVar_hsa_circ_74842,RMVar_hsa_circ_171051 7869 RMVar_ID_7869 Human_SNP_ID_574683100 A-to-I Human chr15 + 41355741 41355741 41355741 CTCTGTTGCCCAGGCTGGAGTGCAGTTGCGCGATCTCGGCTCACTGCAAGTTCCGCCTCCCGGGT CTCTGTTGCCCAGGCTGGAGTGCAGTTGCGCGGTCTCGGCTCACTGCAAGTTCCGCCTCCCGGGT A G NUSAP1,AC087721.2 Ensembl:ENSG00000137804,Ensembl:ENSG00000285920 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs547440668 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99120,RMVar_hsa_circ_66562,RMVar_hsa_circ_171049,RMVar_hsa_circ_68859,RMVar_hsa_circ_64721,RMVar_hsa_circ_58522,RMVar_hsa_circ_26884,RMVar_hsa_circ_303269,RMVar_hsa_circ_335592,RMVar_hsa_circ_36821,RMVar_hsa_circ_355511,RMVar_hsa_circ_55546,RMVar_hsa_circ_74842,RMVar_hsa_circ_171051 7870 RMVar_ID_7870 Human_SNP_ID_574683610 A-to-I Human chr15 + 41357561 41357561 41357561 CACCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGTGTCCCGAGTAGCTGGGATTACAGGCGTGCG CACCTCCCGGGTTCAAGCGATTCTCCTGCCTCGGTGTCCCGAGTAGCTGGGATTACAGGCGTGCG A G NUSAP1,AC087721.2 Ensembl:ENSG00000137804,Ensembl:ENSG00000285920 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1004943185 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99120,RMVar_hsa_circ_171049,RMVar_hsa_circ_68859,RMVar_hsa_circ_64721,RMVar_hsa_circ_271619,RMVar_hsa_circ_58522,RMVar_hsa_circ_26884,RMVar_hsa_circ_303269,RMVar_hsa_circ_335592,RMVar_hsa_circ_355511,RMVar_hsa_circ_55546,RMVar_hsa_circ_74842,RMVar_hsa_circ_171051,RMVar_hsa_circ_290985,RMVar_hsa_circ_302110,RMVar_hsa_circ_326781,RMVar_hsa_circ_274675,RMVar_hsa_circ_171054,RMVar_hsa_circ_171056,RMVar_hsa_circ_97704,RMVar_hsa_circ_171055,RMVar_hsa_circ_171052,RMVar_hsa_circ_171053 7871 RMVar_ID_7871 Human_SNP_ID_574684094 A-to-I Human chr15 + 41359695 41359695 41359695 CTCTTGTTGCCCAGACTGGAGGGCAATGGTACAGTCTCAGCTCACTGCAACCTCTGCCTCCCTGA CTCTTGTTGCCCAGACTGGAGGGCAATGGTACGGTCTCAGCTCACTGCAACCTCTGCCTCCCTGA A G NUSAP1,AC087721.2 Ensembl:ENSG00000137804,Ensembl:ENSG00000285920 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1475417702 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99120,RMVar_hsa_circ_171049,RMVar_hsa_circ_64721,RMVar_hsa_circ_271619,RMVar_hsa_circ_26884,RMVar_hsa_circ_335592,RMVar_hsa_circ_355511,RMVar_hsa_circ_74842,RMVar_hsa_circ_171051,RMVar_hsa_circ_302110,RMVar_hsa_circ_326781,RMVar_hsa_circ_274675,RMVar_hsa_circ_171054,RMVar_hsa_circ_97704,RMVar_hsa_circ_171055,RMVar_hsa_circ_171052,RMVar_hsa_circ_171053,RMVar_hsa_circ_365954 7872 RMVar_ID_7872 Human_SNP_ID_574685093 A-to-I Human chr15 + 41363573 41363573 41363573 TTTTTCAGTTTTTTGTAGAGACAGGCCTCCCTATGTTGTCCAGGCTGGTCTCAAACTCCTAGGCT TTTTTCAGTTTTTTGTAGAGACAGGCCTCCCTGTGTTGTCCAGGCTGGTCTCAAACTCCTAGGCT A G NUSAP1,AC087721.2 Ensembl:ENSG00000137804,Ensembl:ENSG00000285920 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs891890349 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99120,RMVar_hsa_circ_171049,RMVar_hsa_circ_64721,RMVar_hsa_circ_271619,RMVar_hsa_circ_26884,RMVar_hsa_circ_335592,RMVar_hsa_circ_355511,RMVar_hsa_circ_74842,RMVar_hsa_circ_171051,RMVar_hsa_circ_302110,RMVar_hsa_circ_326781,RMVar_hsa_circ_274675,RMVar_hsa_circ_171054,RMVar_hsa_circ_97704,RMVar_hsa_circ_171055,RMVar_hsa_circ_171052,RMVar_hsa_circ_171053,RMVar_hsa_circ_365954 7873 RMVar_ID_7873 Human_SNP_ID_574686501 A-to-I Human chr15 + 41369288 41369288 41369288 AGTTTTTCAAACTTAAAAATGGCTTTAAGTTTAGAATTCTATTTATTGAATTAGCTTGGAATATG AGTTTTTCAAACTTAAAAATGGCTTTAAGTTTCGAATTCTATTTATTGAATTAGCTTGGAATATG A C NUSAP1,AC087721.2 Ensembl:ENSG00000137804,Ensembl:ENSG00000285920 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs372182924 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12503566 RMVar_hsa_circ_99120,RMVar_hsa_circ_171049,RMVar_hsa_circ_64721,RMVar_hsa_circ_50013,RMVar_hsa_circ_271619,RMVar_hsa_circ_26884,RMVar_hsa_circ_335592,RMVar_hsa_circ_74842,RMVar_hsa_circ_326781,RMVar_hsa_circ_274675,RMVar_hsa_circ_171054,RMVar_hsa_circ_97704,RMVar_hsa_circ_171052,RMVar_hsa_circ_171053,RMVar_hsa_circ_365954,RMVar_hsa_circ_14501,RMVar_hsa_circ_48944 7874 RMVar_ID_7874 Human_SNP_ID_574687693 A-to-I Human chr15 + 41373624 41373624 41373624 AGTGCCCGCCACCACGCCCGGCTAATTTTTGTATTTTTGGTAGAGACAGGGTGTCACCGTATTGG AGTGCCCGCCACCACGCCCGGCTAATTTTTGTGTTTTTGGTAGAGACAGGGTGTCACCGTATTGG A G NUSAP1,AC087721.2 Ensembl:ENSG00000137804,Ensembl:ENSG00000285920 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1216435080 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12503642 RMVar_hsa_circ_99120,RMVar_hsa_circ_171049,RMVar_hsa_circ_64721,RMVar_hsa_circ_50013,RMVar_hsa_circ_271619,RMVar_hsa_circ_335592,RMVar_hsa_circ_74842,RMVar_hsa_circ_274675,RMVar_hsa_circ_171054,RMVar_hsa_circ_97704,RMVar_hsa_circ_171052,RMVar_hsa_circ_171053,RMVar_hsa_circ_365954,RMVar_hsa_circ_171058,RMVar_hsa_circ_312886,RMVar_hsa_circ_14501,RMVar_hsa_circ_325674,RMVar_hsa_circ_171060,RMVar_hsa_circ_105150,RMVar_hsa_circ_171059 7875 RMVar_ID_7875 Human_SNP_ID_574692958 A-to-I Human chr15 - 41390251 41390251 41390251 TATATAAGTAGACAACAATTTTGGCTGGGTCCAGTGGCTCACATCTGTAATCCTAGCACTTTGGG TATATAAGTAGACAACAATTTTGGCTGGGTCCTGTGGCTCACATCTGTAATCCTAGCACTTTGGG T A NDUFAF1 Ensembl:ENSG00000137806 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs562784575 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12503835 7876 RMVar_ID_7876 Human_SNP_ID_574693266 A-to-I Human chr15 - 41391378 41391378 41391378 GACATCAAGTGATCCACCCGACTCGCCTCCCAAGGTATTGGGATTATAGGCGTTTGAGCCACCAC GACATCAAGTGATCCACCCGACTCGCCTCCCAGGGTATTGGGATTATAGGCGTTTGAGCCACCAC T C NDUFAF1 Ensembl:ENSG00000137806 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs561834076 Functional Loss SNV dbSNP153 33..33 33 - - - 7877 RMVar_ID_7877 Human_SNP_ID_574693286 A-to-I Human chr15 - 41391437 41391437 41391437 TATTTTTAGGAGAGATGGGGTTTCATTCACCAAGTTGGCCAGGCTGGTTTCGAACTCCTGACATC TATTTTTAGGAGAGATGGGGTTTCATTCACCAGGTTGGCCAGGCTGGTTTCGAACTCCTGACATC T C NDUFAF1 Ensembl:ENSG00000137806 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1258122171 Functional Loss SNV dbSNP153 33..33 33 - - - 7878 RMVar_ID_7878 Human_SNP_ID_574694052 A-to-I Human chr15 - 41393982 41393982 41393982 GTCCTAGGCCAGGCGTGGTGGCTCATGTCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGTAA GTCCTAGGCCAGGCGTGGTGGCTCATGTCTGTGATCCCAGCACTTTGGGAGGCCAAGGTGGGTAA T C NDUFAF1 Ensembl:ENSG00000137806 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1004507798 Functional Loss SNV dbSNP153 33..33 33 - - - 7879 RMVar_ID_7879 Human_SNP_ID_574694123 A-to-I Human chr15 - 41394056 41394056 41394056 TCATTGCACTCCAGCCTGGGCAACAAGAGCCAAACTTTGTCTCAAAAAAAAAAAAAAAAAAAAAA TCATTGCACTCCAGCCTGGGCAACAAGAGCCAGACTTTGTCTCAAAAAAAAAAAAAAAAAAAAAA T C NDUFAF1 Ensembl:ENSG00000137806 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1191626597 Functional Loss SNV dbSNP153 33..33 33 - - - 7880 RMVar_ID_7880 Human_SNP_ID_574702565 A-to-I Human chr15 + 41423463 41423463 41423463 GGCACGCTGGGCTCACTGTAGCCTCCGCCTCTAGGTTCAAGTGATTCTCCTGCCTTAGCCTCCCG GGCACGCTGGGCTCACTGTAGCCTCCGCCTCTGGGTTCAAGTGATTCTCCTGCCTTAGCCTCCCG A G RTF1 Ensembl:ENSG00000137815 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1236756842 Functional Loss SNV dbSNP153 33..33 33 - - - 7881 RMVar_ID_7881 Human_SNP_ID_574703064 A-to-I Human chr15 + 41425287 41425287 41425287 CTGTGTCCGGCTAATTTTTTTTTTGTATTTTTAGTAGGCACGGGTTTCACCATGTTAGCCAGGAT CTGTGTCCGGCTAATTTTTTTTTTGTATTTTTGGTAGGCACGGGTTTCACCATGTTAGCCAGGAT A G RTF1 Ensembl:ENSG00000137815 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417370690 Functional Loss SNV dbSNP153 33..33 33 - - - 7882 RMVar_ID_7882 Human_SNP_ID_574706966 A-to-I Human chr15 + 41438674 41438674 41438674 CCTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCTGTCTCTACTAAAAATAC CCTGAGGTCAGGAGTTCGAGACCAGCCTGGCCGACATGGTGAAACCCTGTCTCTACTAAAAATAC A G RTF1 Ensembl:ENSG00000137815 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1185686280 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_124587 RMVar_hsa_circ_354186,RMVar_hsa_circ_359950,RMVar_hsa_circ_365252,RMVar_hsa_circ_347353,RMVar_hsa_circ_265896,RMVar_hsa_circ_285994,RMVar_hsa_circ_171066 7883 RMVar_ID_7883 Human_SNP_ID_574706996 A-to-I Human chr15 + 41438753 41438753 41438753 CGTGGTGGTGCACGCCTGTAATCCCAGCTACTAAGGAGGCTGAGGCAGGAGAATTGCTTGAACTC CGTGGTGGTGCACGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAACTC A C RTF1 Ensembl:ENSG00000137815 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs918522518 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_354186,RMVar_hsa_circ_359950,RMVar_hsa_circ_365252,RMVar_hsa_circ_347353,RMVar_hsa_circ_265896,RMVar_hsa_circ_285994,RMVar_hsa_circ_171066 7884 RMVar_ID_7884 Human_SNP_ID_574706997 A-to-I Human chr15 + 41438753 41438753 41438753 CGTGGTGGTGCACGCCTGTAATCCCAGCTACTAAGGAGGCTGAGGCAGGAGAATTGCTTGAACTC CGTGGTGGTGCACGCCTGTAATCCCAGCTACTGAGGAGGCTGAGGCAGGAGAATTGCTTGAACTC A G RTF1 Ensembl:ENSG00000137815 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs918522518 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_354186,RMVar_hsa_circ_359950,RMVar_hsa_circ_365252,RMVar_hsa_circ_347353,RMVar_hsa_circ_265896,RMVar_hsa_circ_285994,RMVar_hsa_circ_171066 7885 RMVar_ID_7885 Human_SNP_ID_574706998 A-to-I Human chr15 + 41438753 41438753 41438753 CGTGGTGGTGCACGCCTGTAATCCCAGCTACTAAGGAGGCTGAGGCAGGAGAATTGCTTGAACTC CGTGGTGGTGCACGCCTGTAATCCCAGCTACTTAGGAGGCTGAGGCAGGAGAATTGCTTGAACTC A T RTF1 Ensembl:ENSG00000137815 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs918522518 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_354186,RMVar_hsa_circ_359950,RMVar_hsa_circ_365252,RMVar_hsa_circ_347353,RMVar_hsa_circ_265896,RMVar_hsa_circ_285994,RMVar_hsa_circ_171066 7886 RMVar_ID_7886 Human_SNP_ID_574708066 A-to-I Human chr15 + 41442428 41442428 41442428 TGACCTCATGATCCGCCGGCCTCATCCTCCCAAAGTGCTGGGATCACAGGTGTGAGCCACCATCA TGACCTCATGATCCGCCGGCCTCATCCTCCCAGAGTGCTGGGATCACAGGTGTGAGCCACCATCA A G RTF1 Ensembl:ENSG00000137815 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1171455479 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_354186,RMVar_hsa_circ_359950,RMVar_hsa_circ_365252,RMVar_hsa_circ_347353,RMVar_hsa_circ_265896,RMVar_hsa_circ_285994,RMVar_hsa_circ_171066 7887 RMVar_ID_7887 Human_SNP_ID_574712321 A-to-I Human chr15 + 41459291 41459291 41459291 GGTACTTGGGAGGCTGAGTCAGCAGGAGTATCATTTGAGCCCGGAATGTAGAGTTTGCAATGAGC GGTACTTGGGAGGCTGAGTCAGCAGGAGTATCCTTTGAGCCCGGAATGTAGAGTTTGCAATGAGC A C RTF1 Ensembl:ENSG00000137815 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1430823607 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12504059 RMVar_hsa_circ_71070,RMVar_hsa_circ_359950,RMVar_hsa_circ_365252,RMVar_hsa_circ_347353,RMVar_hsa_circ_265896,RMVar_hsa_circ_322430,RMVar_hsa_circ_171066,RMVar_hsa_circ_358885,RMVar_hsa_circ_21735,RMVar_hsa_circ_341781,RMVar_hsa_circ_50026,RMVar_hsa_circ_67672,RMVar_hsa_circ_355015,RMVar_hsa_circ_89538,RMVar_hsa_circ_23082,RMVar_hsa_circ_171068,RMVar_hsa_circ_171069 7888 RMVar_ID_7888 Human_SNP_ID_574726777 A-to-I Human chr15 - 41509693 41509693 41509693 CACCATGCCCGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGTCAGGCTAG CACCATGCCCGGCTAATTTTTGTATTTTTAGTTGAGATGGGGTTTCACCATGTTGGTCAGGCTAG T A LTK Ensembl:ENSG00000062524 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1045316721 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_124170 RMVar_hsa_circ_41735 7889 RMVar_ID_7889 Human_SNP_ID_574726811 A-to-I Human chr15 - 41509819 41509818 41509819 GTCTGGCTCTGTTGCCCAGGCTGGAGTGCAGTAGTACAAATCTCAGCTCACTGCAACCTCCGCCT GTCTGGCTCTGTTGCCCAGGCTGGAGTGCAGT_GTACAAATCTCAGCTCACTGCAACCTCCGCCT CT C LTK Ensembl:ENSG00000062524 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1566871421 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_41735 7890 RMVar_ID_7890 Human_SNP_ID_574729248 A-to-I Human chr15 - 41517332 41517332 41517332 CATCCTGATATCTGGGGCTTCTGAAGGTCTGTACTGGGAGTGAAGAGTGGCTTAGCTATTTACCC CATCCTGATATCTGGGGCTTCTGAAGGTCTGTGCTGGGAGTGAAGAGTGGCTTAGCTATTTACCC T C RPAP1 Ensembl:ENSG00000103932 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs11070333 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5113121,Human_RBP_ID_9052109,Human_RBP_ID_18189654,Human_RBP_ID_23208837 RMVar_hsa_circ_112881,RMVar_hsa_circ_117726,RMVar_hsa_circ_121854,RMVar_hsa_circ_122638,RMVar_hsa_circ_116277,RMVar_hsa_circ_171078,RMVar_hsa_circ_171082,RMVar_hsa_circ_80485,RMVar_hsa_circ_100795,RMVar_hsa_circ_171083,RMVar_hsa_circ_171084,RMVar_hsa_circ_171080,RMVar_hsa_circ_171081,RMVar_hsa_circ_171079 7891 RMVar_ID_7891 Human_SNP_ID_574729658 A-to-I Human chr15 - 41518618 41518618 41518618 CTGGAGTGCAGTGGCGCGCTCGGCTCACTGCAACCTCCGCCCCTGGGTTCAAGCGACTCCCCTGC CTGGAGTGCAGTGGCGCGCTCGGCTCACTGCAGCCTCCGCCCCTGGGTTCAAGCGACTCCCCTGC T C RPAP1 Ensembl:ENSG00000103932 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1047232598 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112881,RMVar_hsa_circ_117726,RMVar_hsa_circ_122638,RMVar_hsa_circ_116277,RMVar_hsa_circ_171082,RMVar_hsa_circ_80485,RMVar_hsa_circ_171083,RMVar_hsa_circ_171084,RMVar_hsa_circ_171080,RMVar_hsa_circ_171081 7892 RMVar_ID_7892 Human_SNP_ID_574730033 A-to-I Human chr15 - 41520189 41520188 41520189 TGGCTCACGCCTGTAATTCCATCACTCTGGGAAGCTGAGGTGGGTGGATCACTTAAGGTCAGGAG TGGCTCACGCCTGTAATTCCATCACTCTGGGA_GCTGAGGTGGGTGGATCACTTAAGGTCAGGAG CT C RPAP1 Ensembl:ENSG00000103932 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1411320461 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_112881,RMVar_hsa_circ_117726,RMVar_hsa_circ_122638,RMVar_hsa_circ_116277,RMVar_hsa_circ_171082,RMVar_hsa_circ_80485,RMVar_hsa_circ_171083,RMVar_hsa_circ_171084,RMVar_hsa_circ_171080,RMVar_hsa_circ_171081 7893 RMVar_ID_7893 Human_SNP_ID_574734599 A-to-I Human chr15 - 41534523 41534523 41534523 GGAATGCAGTGGCACGATCTCGGCTCACTGCAACCTCCACCTTCACGGCTCAAGCAATCCTCCCA GGAATGCAGTGGCACGATCTCGGCTCACTGCAGCCTCCACCTTCACGGCTCAAGCAATCCTCCCA T C RPAP1 Ensembl:ENSG00000103932 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1185522013 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122638,RMVar_hsa_circ_171084,RMVar_hsa_circ_115870,RMVar_hsa_circ_113089,RMVar_hsa_circ_13078,RMVar_hsa_circ_171086,RMVar_hsa_circ_93979,RMVar_hsa_circ_171087,RMVar_hsa_circ_124804,RMVar_hsa_circ_171085,RMVar_hsa_circ_92112,RMVar_hsa_circ_171093,RMVar_hsa_circ_55731,RMVar_hsa_circ_171094,RMVar_hsa_circ_123132,RMVar_hsa_circ_171096,RMVar_hsa_circ_42218 7894 RMVar_ID_7894 Human_SNP_ID_574734600 A-to-I Human chr15 - 41534523 41534523 41534523 GGAATGCAGTGGCACGATCTCGGCTCACTGCAACCTCCACCTTCACGGCTCAAGCAATCCTCCCA GGAATGCAGTGGCACGATCTCGGCTCACTGCACCCTCCACCTTCACGGCTCAAGCAATCCTCCCA T G RPAP1 Ensembl:ENSG00000103932 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1185522013 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122638,RMVar_hsa_circ_171084,RMVar_hsa_circ_115870,RMVar_hsa_circ_113089,RMVar_hsa_circ_13078,RMVar_hsa_circ_171086,RMVar_hsa_circ_93979,RMVar_hsa_circ_171087,RMVar_hsa_circ_124804,RMVar_hsa_circ_171085,RMVar_hsa_circ_92112,RMVar_hsa_circ_171093,RMVar_hsa_circ_55731,RMVar_hsa_circ_171094,RMVar_hsa_circ_123132,RMVar_hsa_circ_171096,RMVar_hsa_circ_42218 7895 RMVar_ID_7895 Human_SNP_ID_574748075 A-to-I Human chr15 + 41583248 41583248 41583248 TCGATCTCCTGACCTCGTGATCTGCCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCTTCAG TCGATCTCCTGACCTCGTGATCTGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCTTCAG A G TYRO3 Ensembl:ENSG00000092445 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs995300811 Functional Loss SNV dbSNP153 33..33 33 - - - 7896 RMVar_ID_7896 Human_SNP_ID_574758929 A-to-I Human chr15 + 41624518 41624518 41624518 CACCACACCTAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACTATATTGGCCAGGCTGG CACCACACCTAGCTAATTTTTGTATTTTTAGTGGAGACGGGGTTTCACTATATTGGCCAGGCTGG A G MGA Ensembl:ENSG00000174197 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1194473312 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103369,RMVar_hsa_circ_171106 7897 RMVar_ID_7897 Human_SNP_ID_574773457 A-to-I Human chr15 + 41679055 41679055 41679055 GAGATTCCATTTTCTTTTCTTTTTCTTTTTTGAGACTGAGTCTTGCTCTGTTTCCCAGGCTGGAA GAGATTCCATTTTCTTTTCTTTTTCTTTTTTGTGACTGAGTCTTGCTCTGTTTCCCAGGCTGGAA A T MGA Ensembl:ENSG00000174197 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1333787848 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12505071 RMVar_hsa_circ_62516,RMVar_hsa_circ_267133,RMVar_hsa_circ_289216,RMVar_hsa_circ_361602,RMVar_hsa_circ_362942,RMVar_hsa_circ_293603,RMVar_hsa_circ_99996,RMVar_hsa_circ_119055,RMVar_hsa_circ_63725,RMVar_hsa_circ_171110,RMVar_hsa_circ_28966,RMVar_hsa_circ_61298,RMVar_hsa_circ_171112,RMVar_hsa_circ_171111,RMVar_hsa_circ_171108,RMVar_hsa_circ_171109 7898 RMVar_ID_7898 Human_SNP_ID_574781845 A-to-I Human chr15 + 41709330 41709329 41709330 AGATCACACCACTGCACTCCAGCCGGAGTGACAGAGCGAGACCCTGTCTCAAACAAACAAACAAA AGATCACACCACTGCACTCCAGCCGGAGTGAC_GAGCGAGACCCTGTCTCAAACAAACAAACAAA CA C MGA Ensembl:ENSG00000174197 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1239919935 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_62516,RMVar_hsa_circ_267133,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_51708,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_322677,RMVar_hsa_circ_68198,RMVar_hsa_circ_286685,RMVar_hsa_circ_17990,RMVar_hsa_circ_46819,RMVar_hsa_circ_171127,RMVar_hsa_circ_171128 7899 RMVar_ID_7899 Human_SNP_ID_574783311 A-to-I Human chr15 + 41714693 41714693 41714693 TTTTTATATTTTAGTAGAGACGGGGTTTCACCATGTTGCGTAGGCTGGTCTTGAACTCCTGAGCT TTTTTATATTTTAGTAGAGACGGGGTTTCACCGTGTTGCGTAGGCTGGTCTTGAACTCCTGAGCT A G MGA Ensembl:ENSG00000174197 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1437888380 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_62516,RMVar_hsa_circ_361602,RMVar_hsa_circ_362942,RMVar_hsa_circ_99996,RMVar_hsa_circ_63725,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_127319,RMVar_hsa_circ_76617,RMVar_hsa_circ_103973,RMVar_hsa_circ_171116,RMVar_hsa_circ_171120,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_17990,RMVar_hsa_circ_50622,RMVar_hsa_circ_171128,RMVar_hsa_circ_358555,RMVar_hsa_circ_368129,RMVar_hsa_circ_375598,RMVar_hsa_circ_57489,RMVar_hsa_circ_171129 7900 RMVar_ID_7900 Human_SNP_ID_574789610 A-to-I Human chr15 + 41738585 41738585 41738585 TTGAAAACAGAGGTTTGCCTGATACAATTTCTAGTGAGACTAGACTCCCTAAAATACAAGCATGG TTGAAAACAGAGGTTTGCCTGATACAATTTCTGGTGAGACTAGACTCCCTAAAATACAAGCATGG A G MGA Ensembl:ENSG00000174197 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2577951 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_624,GWAS_ID_625,GWAS_ID_626,GWAS_ID_627 RMVar_hsa_circ_62516,RMVar_hsa_circ_99996,RMVar_hsa_circ_63725,RMVar_hsa_circ_61298,RMVar_hsa_circ_171108,RMVar_hsa_circ_328073,RMVar_hsa_circ_267209,RMVar_hsa_circ_127319,RMVar_hsa_circ_76617,RMVar_hsa_circ_103973,RMVar_hsa_circ_1212,RMVar_hsa_circ_171116,RMVar_hsa_circ_171117,RMVar_hsa_circ_171114,RMVar_hsa_circ_171115,RMVar_hsa_circ_84,RMVar_hsa_circ_50622,RMVar_hsa_circ_358555,RMVar_hsa_circ_64804,RMVar_hsa_circ_353908,RMVar_hsa_circ_24182,RMVar_hsa_circ_6130,RMVar_hsa_circ_34392,RMVar_hsa_circ_267676,RMVar_hsa_circ_367661,RMVar_hsa_circ_313219,RMVar_hsa_circ_110263,RMVar_hsa_circ_81076,RMVar_hsa_circ_171133,RMVar_hsa_circ_171134 7901 RMVar_ID_7901 Human_SNP_ID_574789611 A-to-I Human chr15 + 41738585 41738585 41738585 TTGAAAACAGAGGTTTGCCTGATACAATTTCTAGTGAGACTAGACTCCCTAAAATACAAGCATGG TTGAAAACAGAGGTTTGCCTGATACAATTTCTTGTGAGACTAGACTCCCTAAAATACAAGCATGG A T MGA Ensembl:ENSG00000174197 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2577951 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_624,GWAS_ID_625,GWAS_ID_626,GWAS_ID_627 RMVar_hsa_circ_62516,RMVar_hsa_circ_99996,RMVar_hsa_circ_63725,RMVar_hsa_circ_61298,RMVar_hsa_circ_171108,RMVar_hsa_circ_328073,RMVar_hsa_circ_267209,RMVar_hsa_circ_127319,RMVar_hsa_circ_76617,RMVar_hsa_circ_103973,RMVar_hsa_circ_1212,RMVar_hsa_circ_171116,RMVar_hsa_circ_171117,RMVar_hsa_circ_171114,RMVar_hsa_circ_171115,RMVar_hsa_circ_84,RMVar_hsa_circ_50622,RMVar_hsa_circ_358555,RMVar_hsa_circ_64804,RMVar_hsa_circ_353908,RMVar_hsa_circ_24182,RMVar_hsa_circ_6130,RMVar_hsa_circ_34392,RMVar_hsa_circ_267676,RMVar_hsa_circ_367661,RMVar_hsa_circ_313219,RMVar_hsa_circ_110263,RMVar_hsa_circ_81076,RMVar_hsa_circ_171133,RMVar_hsa_circ_171134 7902 RMVar_ID_7902 Human_SNP_ID_574793224 A-to-I Human chr15 + 41751578 41751578 41751578 AAACCCCGTGTCTACTAAAAATACAAAAAATTAGCCAGGTGTGGTGATGGGTGCCTGTAATCCCA AAACCCCGTGTCTACTAAAAATACAAAAAATTCGCCAGGTGTGGTGATGGGTGCCTGTAATCCCA A C MGA Ensembl:ENSG00000174197 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1365009367 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_631,RMVar_hsa_circ_63725,RMVar_hsa_circ_61298,RMVar_hsa_circ_267209,RMVar_hsa_circ_127319,RMVar_hsa_circ_76617,RMVar_hsa_circ_103973,RMVar_hsa_circ_171116,RMVar_hsa_circ_171114,RMVar_hsa_circ_171115,RMVar_hsa_circ_84,RMVar_hsa_circ_358555,RMVar_hsa_circ_64804,RMVar_hsa_circ_24182,RMVar_hsa_circ_367661,RMVar_hsa_circ_81076,RMVar_hsa_circ_98042,RMVar_hsa_circ_171134,RMVar_hsa_circ_328827,RMVar_hsa_circ_115588,RMVar_hsa_circ_171137,RMVar_hsa_circ_171138,RMVar_hsa_circ_30975,RMVar_hsa_circ_296087,RMVar_hsa_circ_171140,RMVar_hsa_circ_333437,RMVar_hsa_circ_171139,RMVar_hsa_circ_343003,RMVar_hsa_circ_322735,RMVar_hsa_circ_274463,RMVar_hsa_circ_171141 7903 RMVar_ID_7903 Human_SNP_ID_574793894 A-to-I Human chr15 + 41754022 41754022 41754022 GTCACTGCAGCCTCGAACTCCTGGCCTCAAGCAATCCTCCCACCTCAGGTTTCCGAGTAGCTGTA GTCACTGCAGCCTCGAACTCCTGGCCTCAAGCGATCCTCCCACCTCAGGTTTCCGAGTAGCTGTA A G MGA Ensembl:ENSG00000174197 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1009962752 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_631,RMVar_hsa_circ_63725,RMVar_hsa_circ_61298,RMVar_hsa_circ_267209,RMVar_hsa_circ_127319,RMVar_hsa_circ_76617,RMVar_hsa_circ_103973,RMVar_hsa_circ_171116,RMVar_hsa_circ_171114,RMVar_hsa_circ_171115,RMVar_hsa_circ_84,RMVar_hsa_circ_358555,RMVar_hsa_circ_64804,RMVar_hsa_circ_24182,RMVar_hsa_circ_367661,RMVar_hsa_circ_81076,RMVar_hsa_circ_98042,RMVar_hsa_circ_171134,RMVar_hsa_circ_328827,RMVar_hsa_circ_115588,RMVar_hsa_circ_171137,RMVar_hsa_circ_171138,RMVar_hsa_circ_30975,RMVar_hsa_circ_296087,RMVar_hsa_circ_171140,RMVar_hsa_circ_333437,RMVar_hsa_circ_171139,RMVar_hsa_circ_343003,RMVar_hsa_circ_322735,RMVar_hsa_circ_274463,RMVar_hsa_circ_171141 7904 RMVar_ID_7904 Human_SNP_ID_574796453 A-to-I Human chr15 + 41763658 41763658 41763658 TCAGCTATTTAGGAGGCTGAGGCAGGAGAATCACTTTAACCCGGAAGGTGGAAGTTGTGGTGAGC TCAGCTATTTAGGAGGCTGAGGCAGGAGAATCGCTTTAACCCGGAAGGTGGAAGTTGTGGTGAGC A G MGA Ensembl:ENSG00000174197 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1197769 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_628,GWAS_ID_629,GWAS_ID_630,GWAS_ID_631,GWAS_ID_632,GWAS_ID_633,GWAS_ID_634 RMVar_hsa_circ_127319,RMVar_hsa_circ_76617,RMVar_hsa_circ_171114,RMVar_hsa_circ_171115,RMVar_hsa_circ_339736 7905 RMVar_ID_7905 Human_SNP_ID_574798393 A-to-I Human chr15 + 41770923 41770923 41770923 TGGAGTGCAGTGGTGCCGTCTTGGCTCACTGCAAGCTCTGCCTCCCGGGTTTACGCCATTGTCCT TGGAGTGCAGTGGTGCCGTCTTGGCTCACTGCGAGCTCTGCCTCCCGGGTTTACGCCATTGTCCT A G MGA Ensembl:ENSG00000174197 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1385198532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12506370 7906 RMVar_ID_7906 Human_SNP_ID_574798410 A-to-I Human chr15 + 41770973 41770973 41770973 TTACGCCATTGTCCTGCCTCAGCCTCCGGAGTAGCTGGGACTACAGGCGCCCGACACTGTGCCCG TTACGCCATTGTCCTGCCTCAGCCTCCGGAGTGGCTGGGACTACAGGCGCCCGACACTGTGCCCG A G MGA Ensembl:ENSG00000174197 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs969750441 Functional Loss SNV dbSNP153 33..33 33 - - - 7907 RMVar_ID_7907 Human_SNP_ID_574801185 A-to-I Human chr15 + 41781520 41781520 41781520 CCCTGCTATGCCGGGCATGGTGGTGCACACCTATAGCCCCAGCATCTTAGGAGGCTGAGGCGGGA CCCTGCTATGCCGGGCATGGTGGTGCACACCTGTAGCCCCAGCATCTTAGGAGGCTGAGGCGGGA A G MAPKBP1 Ensembl:ENSG00000137802 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1449805192 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99150,RMVar_hsa_circ_171150 7908 RMVar_ID_7908 Human_SNP_ID_574805636 A-to-I Human chr15 + 41798376 41798376 41798376 GTGATCTCGGCTCACTGCAACCTCCACCTCCCAGGTTCAAATGAATCTCATGCCTCAGCCTCCTG GTGATCTCGGCTCACTGCAACCTCCACCTCCCGGGTTCAAATGAATCTCATGCCTCAGCCTCCTG A G MAPKBP1 Ensembl:ENSG00000137802 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs918314707 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99150,RMVar_hsa_circ_171150 7909 RMVar_ID_7909 Human_SNP_ID_574814694 A-to-I Human chr15 + 41829921 41829921 41829921 TGAGACACCATCGTGTGGTGGCATGTGCCTGTAGTCCCACCTCCTGAGGCAAGAGGATTGTTTGA TGAGACACCATCGTGTGGTGGCATGTGCCTGTGGTCCCACCTCCTGAGGCAAGAGGATTGTTTGA A G JMJD7-PLA2G4B,JMJD7 Ensembl:ENSG00000168970,Ensembl:ENSG00000243789 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935708012 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12507277 RMVar_hsa_circ_171153,RMVar_hsa_circ_97423 7910 RMVar_ID_7910 Human_SNP_ID_574815923 A-to-I Human chr15 + 41833629 41833629 41833629 TTTTTGTAGAGATGGGGTCTCCCTACGTTGCCAAGGCTGGTCTTGACCTCCCGGCCTCAGCAATC TTTTTGTAGAGATGGGGTCTCCCTACGTTGCCGAGGCTGGTCTTGACCTCCCGGCCTCAGCAATC A G JMJD7-PLA2G4B,JMJD7 Ensembl:ENSG00000168970,Ensembl:ENSG00000243789 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1384323988 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_171153,RMVar_hsa_circ_97423 7911 RMVar_ID_7911 Human_SNP_ID_574844218 A-to-I Human chr15 - 41915135 41915135 41915135 AATGTATATGTAGTTCACACTTACACTCTGACACAGATCTCATTGTGTCCAATGATGTGTGTGTG AATGTATATGTAGTTCACACTTACACTCTGACGCAGATCTCATTGTGTCCAATGATGTGTGTGTG T C EHD4 Ensembl:ENSG00000103966 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1184956345 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37826,RMVar_hsa_circ_91169,RMVar_hsa_circ_171166 7912 RMVar_ID_7912 Human_SNP_ID_574844235 A-to-I Human chr15 - 41915214 41915214 41915214 AAATGACAAAATGACAGTTTTTCTCTAGGCTAATAACTCAATGAGCAGAAAGGAAAGTCCTCCCT AAATGACAAAATGACAGTTTTTCTCTAGGCTAGTAACTCAATGAGCAGAAAGGAAAGTCCTCCCT T C EHD4 Ensembl:ENSG00000103966 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1232719339 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37826,RMVar_hsa_circ_91169,RMVar_hsa_circ_171166 7913 RMVar_ID_7913 Human_SNP_ID_574850122 A-to-I Human chr15 - 41940100 41940100 41940100 CTCAAAAGCTGAGTGGCTGGGCGCGGTGGCTCACGCCTATAATCCCAGCCCTTTGGGAGGCCGAG CTCAAAAGCTGAGTGGCTGGGCGCGGTGGCTCCCGCCTATAATCCCAGCCCTTTGGGAGGCCGAG T G EHD4 Ensembl:ENSG00000103966 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1311588814 Functional Loss SNV dbSNP153 33..33 33 - - - 7914 RMVar_ID_7914 Human_SNP_ID_574855182 A-to-I Human chr15 - 41959960 41959960 41959960 CAATAGAAACTGCTTTTTTTTTTTTTTTTTTGAGGTGGAGTCTCACCCAGTCTGGAATGCAGTGG CAATAGAAACTGCTTTTTTTTTTTTTTTTTTGTGGTGGAGTCTCACCCAGTCTGGAATGCAGTGG T A EHD4 Ensembl:ENSG00000103966 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1263547667 Functional Loss SNV dbSNP153 33..33 33 - - - 7915 RMVar_ID_7915 Human_SNP_ID_574912718 A-to-I Human chr15 - 42181783 42181783 42181783 ATTGCTTGAGCCTGGGAGATGGAGGCGGCAGTAAGCCGTGATCACACCACTCACTGCATTCCAGC ATTGCTTGAGCCTGGGAGATGGAGGCGGCAGTGAGCCGTGATCACACCACTCACTGCATTCCAGC T C VPS39 Ensembl:ENSG00000166887 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1292476604 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4317,RMVar_hsa_circ_5747,RMVar_hsa_circ_35356,RMVar_hsa_circ_76047,RMVar_hsa_circ_7933,RMVar_hsa_circ_31789,RMVar_hsa_circ_87213,RMVar_hsa_circ_171173,RMVar_hsa_circ_348155,RMVar_hsa_circ_367513,RMVar_hsa_circ_369537,RMVar_hsa_circ_171174,RMVar_hsa_circ_171175,RMVar_hsa_circ_171176,RMVar_hsa_circ_306151,RMVar_hsa_circ_342936,RMVar_hsa_circ_365248,RMVar_hsa_circ_337848,RMVar_hsa_circ_115855,RMVar_hsa_circ_125109,RMVar_hsa_circ_86954,RMVar_hsa_circ_98544,RMVar_hsa_circ_81647,RMVar_hsa_circ_171178,RMVar_hsa_circ_171180,RMVar_hsa_circ_171182,RMVar_hsa_circ_171183,RMVar_hsa_circ_171181,RMVar_hsa_circ_171179 7916 RMVar_ID_7916 Human_SNP_ID_574914571 A-to-I Human chr15 - 42189628 42189628 42189628 GACCTCCTGGGTCAAGGGATTCTCCTGCTTCAACCCCCTGAGTAGCTGGGATTACAGGCACCCAC GACCTCCTGGGTCAAGGGATTCTCCTGCTTCAGCCCCCTGAGTAGCTGGGATTACAGGCACCCAC T C VPS39 Ensembl:ENSG00000166887 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1259716572 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25138136 RMVar_hsa_circ_35356,RMVar_hsa_circ_7933,RMVar_hsa_circ_31789,RMVar_hsa_circ_87213,RMVar_hsa_circ_171173,RMVar_hsa_circ_369537,RMVar_hsa_circ_171176,RMVar_hsa_circ_306151,RMVar_hsa_circ_98544,RMVar_hsa_circ_81647,RMVar_hsa_circ_171178,RMVar_hsa_circ_171179,RMVar_hsa_circ_36022,RMVar_hsa_circ_330502,RMVar_hsa_circ_339790,RMVar_hsa_circ_367326,RMVar_hsa_circ_16432,RMVar_hsa_circ_171185,RMVar_hsa_circ_9974 7917 RMVar_ID_7917 Human_SNP_ID_574923321 A-to-I Human chr15 - 42226626 42226626 42226626 CTCTCCTCTTAACTTCATGATTTTTGGCATGCAGCCTCTCCACCTCTCTGGCCTTAGTTTCCTTT CTCTCCTCTTAACTTCATGATTTTTGGCATGCGGCCTCTCCACCTCTCTGGCCTTAGTTTCCTTT T C TMEM87A Ensembl:ENSG00000103978 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1678989 Functional Loss SNV dbSNP153 33..33 33 - - - 7918 RMVar_ID_7918 Human_SNP_ID_574926057 A-to-I Human chr15 - 42237911 42237911 42237911 CTCAAGACAAGATAATGCTTTCATATTAGTTAATGTTAAGCTCCAAAGGAAGAATTATTTCTTAA CTCAAGACAAGATAATGCTTTCATATTAGTTAGTGTTAAGCTCCAAAGGAAGAATTATTTCTTAA T C TMEM87A Ensembl:ENSG00000103978 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4923934 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28828,RMVar_hsa_circ_115584,RMVar_hsa_circ_26833,RMVar_hsa_circ_109570,RMVar_hsa_circ_78896,RMVar_hsa_circ_19735,RMVar_hsa_circ_171189,RMVar_hsa_circ_171190,RMVar_hsa_circ_171192,RMVar_hsa_circ_333728,RMVar_hsa_circ_171191,RMVar_hsa_circ_171193,RMVar_hsa_circ_290554,RMVar_hsa_circ_345413,RMVar_hsa_circ_313245 7919 RMVar_ID_7919 Human_SNP_ID_574931791 A-to-I Human chr15 - 42260122 42260122 42260122 GTAATAGTCTCACTTCAGCCTCCCAAAGTGCTAGGATTATAGGCGTGAGCCACTGCACCTAGCCT GTAATAGTCTCACTTCAGCCTCCCAAAGTGCTGGGATTATAGGCGTGAGCCACTGCACCTAGCCT T C TMEM87A Ensembl:ENSG00000103978 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs912655390 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115584,RMVar_hsa_circ_26833,RMVar_hsa_circ_78896,RMVar_hsa_circ_171189,RMVar_hsa_circ_171190,RMVar_hsa_circ_18371,RMVar_hsa_circ_171192,RMVar_hsa_circ_333728,RMVar_hsa_circ_171193,RMVar_hsa_circ_290554,RMVar_hsa_circ_279379,RMVar_hsa_circ_171195,RMVar_hsa_circ_171196,RMVar_hsa_circ_289473 7920 RMVar_ID_7920 Human_SNP_ID_574936719 A-to-I Human chr15 + 42277816 42277816 42277816 TAGAGAGGGGGTTTCACCATGTTGGTCAGGCTAGTCTTGAATTCCTGACCTCAGATGATCCATCC TAGAGAGGGGGTTTCACCATGTTGGTCAGGCTGGTCTTGAATTCCTGACCTCAGATGATCCATCC A G GANC Ensembl:ENSG00000214013 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956483284 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6504 7921 RMVar_ID_7921 Human_SNP_ID_574936810 A-to-I Human chr15 + 42278003 42278003 42278003 AAAAATTGTATTATACAGTATAGCTTTCTAACATATTCCCTCTCTGTTTAATAGGAAGAAAAGCG AAAAATTGTATTATACAGTATAGCTTTCTAACGTATTCCCTCTCTGTTTAATAGGAAGAAAAGCG A G GANC Ensembl:ENSG00000214013 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs12916523 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22540545 Human_Splice_Rec_1589317,Human_Splice_Rec_1589325 RMVar_hsa_circ_6504 7922 RMVar_ID_7922 Human_SNP_ID_574936811 A-to-I Human chr15 + 42278003 42278003 42278003 AAAAATTGTATTATACAGTATAGCTTTCTAACATATTCCCTCTCTGTTTAATAGGAAGAAAAGCG AAAAATTGTATTATACAGTATAGCTTTCTAACTTATTCCCTCTCTGTTTAATAGGAAGAAAAGCG A T GANC Ensembl:ENSG00000214013 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs12916523 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22540545 Human_Splice_Rec_1589317,Human_Splice_Rec_1589325 RMVar_hsa_circ_6504 7923 RMVar_ID_7923 Human_SNP_ID_574956345 A-to-I Human chr15 + 42354537 42354537 42354537 TAATTTTAATAAAAATATGTGGGGGTCTCACTATGTTGCCCAGGCTAGTCTTGAACTCCCGGACT TAATTTTAATAAAAATATGTGGGGGTCTCACTGTGTTGCCCAGGCTAGTCTTGAACTCCCGGACT A G AC012651.1,GANC Ensembl:ENSG00000258461,Ensembl:ENSG00000214013 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs914242872 Functional Loss SNV dbSNP153 33..33 33 - - - 7924 RMVar_ID_7924 Human_SNP_ID_574972482 A-to-I Human chr15 - 42415959 42415959 42415959 GGGAGGCTGAGGCAGGCAGATCACCTGAGGCTAGGAGTTGCAGACCAGCCTGGCCAACATGGCAA GGGAGGCTGAGGCAGGCAGATCACCTGAGGCTGGGAGTTGCAGACCAGCCTGGCCAACATGGCAA T C ZNF106 Ensembl:ENSG00000103994 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs758000394 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26437539 RMVar_hsa_circ_82168,RMVar_hsa_circ_109960,RMVar_hsa_circ_171206,RMVar_hsa_circ_171207 7925 RMVar_ID_7925 Human_SNP_ID_574974307 A-to-I Human chr15 - 42423150 42423149 42423150 TTGCCCAGGCTGGTCTTGAACTCCTGAGCTCAAGTAATCTGCCCAGCTCGGCCTCCCAAAGTTTT TTGCCCAGGCTGGTCTTGAACTCCTGAGCTCA_GTAATCTGCCCAGCTCGGCCTCCCAAAGTTTT CT C ZNF106 Ensembl:ENSG00000103994 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1209611606 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_18005,RMVar_hsa_circ_82168,RMVar_hsa_circ_109960,RMVar_hsa_circ_171208,RMVar_hsa_circ_171206,RMVar_hsa_circ_171207,RMVar_hsa_circ_333637,RMVar_hsa_circ_365995,RMVar_hsa_circ_376537,RMVar_hsa_circ_49455,RMVar_hsa_circ_171209,RMVar_hsa_circ_87771,RMVar_hsa_circ_125596,RMVar_hsa_circ_267558,RMVar_hsa_circ_171210 7926 RMVar_ID_7926 Human_SNP_ID_574974343 A-to-I Human chr15 - 42423294 42423294 42423294 GCGATCTTGACTCACTGCAGCCTCAACCTCCTAGGCTCAAGGGATCCTCCCACCTCAGCCCCCCA GCGATCTTGACTCACTGCAGCCTCAACCTCCTGGGCTCAAGGGATCCTCCCACCTCAGCCCCCCA T C ZNF106 Ensembl:ENSG00000103994 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1344013760 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18005,RMVar_hsa_circ_82168,RMVar_hsa_circ_109960,RMVar_hsa_circ_171208,RMVar_hsa_circ_171206,RMVar_hsa_circ_171207,RMVar_hsa_circ_333637,RMVar_hsa_circ_365995,RMVar_hsa_circ_376537,RMVar_hsa_circ_49455,RMVar_hsa_circ_171209,RMVar_hsa_circ_87771,RMVar_hsa_circ_125596,RMVar_hsa_circ_267558,RMVar_hsa_circ_171210 7927 RMVar_ID_7927 Human_SNP_ID_574985482 A-to-I Human chr15 - 42465190 42465190 42465190 CACCTTTAAAAAATGAAATGTAGGCCAGGTGCAGTGGCTGATGCCTGTAATCCGAGCATTTTGGA CACCTTTAAAAAATGAAATGTAGGCCAGGTGCCGTGGCTGATGCCTGTAATCCGAGCATTTTGGA T G ZNF106 Ensembl:ENSG00000103994 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1271406288 Functional Loss SNV dbSNP153 33..33 33 - - - 7928 RMVar_ID_7928 Human_SNP_ID_574986218 A-to-I Human chr15 - 42468201 42468201 42468201 ATAGTGGCGCATGCCTGTAATCGAGGCTACTCAGGAGGCTGAGGCAGGAGAAACTCTTGAAACCC ATAGTGGCGCATGCCTGTAATCGAGGCTACTCGGGAGGCTGAGGCAGGAGAAACTCTTGAAACCC T C ZNF106 Ensembl:ENSG00000103994 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1250636267 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16356 7929 RMVar_ID_7929 Human_SNP_ID_574993452 A-to-I Human chr15 + 42496502 42496502 42496502 ACTTTGGGAGGTCGAGGAGAGAGGATCATATGAGATCAGGAGTTCGAGACCAGCCTGGCCAACAT ACTTTGGGAGGTCGAGGAGAGAGGATCATATGCGATCAGGAGTTCGAGACCAGCCTGGCCAACAT A C SNAP23 Ensembl:ENSG00000092531 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1400210350 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116901,RMVar_hsa_circ_171221,RMVar_hsa_circ_92076,RMVar_hsa_circ_171220 7930 RMVar_ID_7930 Human_SNP_ID_574995982 A-to-I Human chr15 + 42507018 42507018 42507018 TTTTTGATTATTTGTAGAGAACGGGTCTCACTATGTTGCCCAGGCTGGTCTTGAATTCCTGGCCT TTTTTGATTATTTGTAGAGAACGGGTCTCACTGTGTTGCCCAGGCTGGTCTTGAATTCCTGGCCT A G SNAP23 Ensembl:ENSG00000092531 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1326786564 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116901,RMVar_hsa_circ_171221,RMVar_hsa_circ_92076,RMVar_hsa_circ_171220 7931 RMVar_ID_7931 Human_SNP_ID_575002069 A-to-I Human chr15 + 42532271 42532271 42532271 TGTCACCACGCTCGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTCAAGCTGGT TGTCACCACGCTCGGCTAATTTTTGTATTTTTCGTAGAGACAGGGTTTCACCATGTCAAGCTGGT A C SNAP23 Ensembl:ENSG00000092531 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs765866602 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_457313 RMVar_hsa_circ_89188,RMVar_hsa_circ_111107,RMVar_hsa_circ_171223,RMVar_hsa_circ_96563,RMVar_hsa_circ_171224,RMVar_hsa_circ_171229 7932 RMVar_ID_7932 Human_SNP_ID_575002075 A-to-I Human chr15 + 42532291 42532291 42532291 TTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTCAAGCTGGTCTTGGACTCCTGACGTCGTG TTTTGTATTTTTAGTAGAGACAGGGTTTCACCGTGTCAAGCTGGTCTTGGACTCCTGACGTCGTG A G SNAP23 Ensembl:ENSG00000092531 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053782508 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_457313 Human_miRNA_ID_1411383 RMVar_hsa_circ_89188,RMVar_hsa_circ_111107,RMVar_hsa_circ_171223,RMVar_hsa_circ_96563,RMVar_hsa_circ_171224,RMVar_hsa_circ_171229 7933 RMVar_ID_7933 Human_SNP_ID_575002076 A-to-I Human chr15 + 42532291 42532291 42532291 TTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTCAAGCTGGTCTTGGACTCCTGACGTCGTG TTTTGTATTTTTAGTAGAGACAGGGTTTCACCTTGTCAAGCTGGTCTTGGACTCCTGACGTCGTG A T SNAP23 Ensembl:ENSG00000092531 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053782508 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_457313 Human_miRNA_ID_1411383 RMVar_hsa_circ_89188,RMVar_hsa_circ_111107,RMVar_hsa_circ_171223,RMVar_hsa_circ_96563,RMVar_hsa_circ_171224,RMVar_hsa_circ_171229 7934 RMVar_ID_7934 Human_SNP_ID_575002079 A-to-I Human chr15 + 42532296 42532296 42532296 TATTTTTAGTAGAGACAGGGTTTCACCATGTCAAGCTGGTCTTGGACTCCTGACGTCGTGATCCA TATTTTTAGTAGAGACAGGGTTTCACCATGTCTAGCTGGTCTTGGACTCCTGACGTCGTGATCCA A T SNAP23 Ensembl:ENSG00000092531 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1196594326 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_457313,Human_RBP_ID_12509087 Human_miRNA_ID_1411383,Human_miRNA_ID_1531974 RMVar_hsa_circ_89188,RMVar_hsa_circ_111107,RMVar_hsa_circ_171223,RMVar_hsa_circ_96563,RMVar_hsa_circ_171224,RMVar_hsa_circ_171229 7935 RMVar_ID_7935 Human_SNP_ID_575002089 A-to-I Human chr15 + 42532345 42532345 42532345 CTGACGTCGTGATCCACCCGCCTTGGCCTCCCAAAGTACTGGGATTACAGGCGTGAGCCACTGTG CTGACGTCGTGATCCACCCGCCTTGGCCTCCCGAAGTACTGGGATTACAGGCGTGAGCCACTGTG A G SNAP23 Ensembl:ENSG00000092531 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1344863499 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2678882,Human_miRNA_ID_3080926 RMVar_hsa_circ_89188,RMVar_hsa_circ_111107,RMVar_hsa_circ_171223,RMVar_hsa_circ_96563,RMVar_hsa_circ_171224,RMVar_hsa_circ_171229 7936 RMVar_ID_7936 Human_SNP_ID_575003507 A-to-I Human chr15 - 42538534 42538534 42538534 AAAAAAATGGAGCCAGGCAGAGGCAGGCATCTATAGTCCCAGCTATTGAGGAGGCCTGAGGCTGG AAAAAAATGGAGCCAGGCAGAGGCAGGCATCTGTAGTCCCAGCTATTGAGGAGGCCTGAGGCTGG T C LRRC57,AC018362.3 Ensembl:ENSG00000180979,Ensembl:ENSG00000285942 Protein coding,Protein coding 3'UTR,intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1015612369 Functional Loss SNV dbSNP153 33..33 33 - - - 7937 RMVar_ID_7937 Human_SNP_ID_575003642 A-to-I Human chr15 - 42539164 42539164 42539164 TATATGTATTTTTTGAGACAGGGTCTTGCTCTATTGCCCAGGCTGAAGTGCAGTGGCATGATCAC TATATGTATTTTTTGAGACAGGGTCTTGCTCTGTTGCCCAGGCTGAAGTGCAGTGGCATGATCAC T C LRRC57,AC018362.3 Ensembl:ENSG00000180979,Ensembl:ENSG00000285942 Protein coding,Protein coding 3'UTR,intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs570578862 Functional Loss SNV dbSNP153 33..33 33 - - - 7938 RMVar_ID_7938 Human_SNP_ID_575003875 A-to-I Human chr15 - 42540004 42540004 42540004 TTTAGTAGAGACGGGGTTTCACCATGTTGGTCAGGCTGATCTCAAACTCCTGACCTCAGTTGATC TTTAGTAGAGACGGGGTTTCACCATGTTGGTCGGGCTGATCTCAAACTCCTGACCTCAGTTGATC T C LRRC57,AC018362.3 Ensembl:ENSG00000180979,Ensembl:ENSG00000285942 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1175313823 Functional Loss SNV dbSNP153 33..33 33 - - - 7939 RMVar_ID_7939 Human_SNP_ID_575004228 A-to-I Human chr15 - 42541392 42541392 42541392 TCAACTGATTCTTGTGCCTCATTCTCCTGAGTAATTGGGATTACAGGCATGCACCACCACACCCA TCAACTGATTCTTGTGCCTCATTCTCCTGAGTCATTGGGATTACAGGCATGCACCACCACACCCA T G LRRC57,AC018362.3 Ensembl:ENSG00000180979,Ensembl:ENSG00000285942 Protein coding,Protein coding 3'UTR,intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1043908825 Functional Loss SNV dbSNP153 33..33 33 - - - 7940 RMVar_ID_7940 Human_SNP_ID_575004616 A-to-I Human chr15 - 42542956 42542956 42542956 TGAGGCAGGAGAATTGCTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCCGAGATCATGCCATTGC TGAGGCAGGAGAATTGCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCCGAGATCATGCCATTGC T C LRRC57,AC018362.3 Ensembl:ENSG00000180979,Ensembl:ENSG00000285942 Protein coding,Protein coding 3'UTR,intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs974000085 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93518,RMVar_hsa_circ_171230 7941 RMVar_ID_7941 Human_SNP_ID_575004764 A-to-I Human chr15 - 42543419 42543419 42543419 AAGGCGGGTGGCTCACTTGAGGCTAGGAGTTCAAGACTAGCGTGGCCAACATGAGGAAACCCTGT AAGGCGGGTGGCTCACTTGAGGCTAGGAGTTCGAGACTAGCGTGGCCAACATGAGGAAACCCTGT T C LRRC57,AC018362.3 Ensembl:ENSG00000180979,Ensembl:ENSG00000285942 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs978435493 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26437544 Human_miRNA_ID_1264669,Human_miRNA_ID_1689199,Human_miRNA_ID_2675542,Human_miRNA_ID_2926293 RMVar_hsa_circ_93518,RMVar_hsa_circ_171230 7942 RMVar_ID_7942 Human_SNP_ID_575004775 A-to-I Human chr15 - 42543475 42543475 42543475 GCACTTTGGCCTGGGCATGGTGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCCAAGGCGGGT GCACTTTGGCCTGGGCATGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGT T C LRRC57,AC018362.3 Ensembl:ENSG00000180979,Ensembl:ENSG00000285942 Protein coding,Protein coding 3'UTR,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1195172757 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21887698,Human_RBP_ID_23209053,Human_RBP_ID_26437545 Human_miRNA_ID_1943015,Human_miRNA_ID_1946060,Human_miRNA_ID_2086690,Human_miRNA_ID_2117206,Human_miRNA_ID_2200786,Human_miRNA_ID_2203849,Human_miRNA_ID_2316356,Human_miRNA_ID_2319511,Human_miRNA_ID_2322669,Human_miRNA_ID_2325841,Human_miRNA_ID_2328951,Human_miRNA_ID_2520218,Human_miRNA_ID_2523380,Human_miRNA_ID_2775214,Human_miRNA_ID_2816307,Human_miRNA_ID_2822579,Human_miRNA_ID_2828702,Human_miRNA_ID_2831861,Human_miRNA_ID_2835981,Human_miRNA_ID_2841335,Human_miRNA_ID_2846440,Human_miRNA_ID_2849461,Human_miRNA_ID_2863570,Human_miRNA_ID_3113302 RMVar_hsa_circ_93518,RMVar_hsa_circ_171230 7943 RMVar_ID_7943 Human_SNP_ID_575004950 A-to-I Human chr15 - 42544303 42544303 42544303 CTACCTTGGCCTCCCAAAGTGTTGAGATTGCAAGTGTGAGCCTCTGCACCTGGCCAAAACTATGT CTACCTTGGCCTCCCAAAGTGTTGAGATTGCAGGTGTGAGCCTCTGCACCTGGCCAAAACTATGT T C LRRC57,AC018362.3 Ensembl:ENSG00000180979,Ensembl:ENSG00000285942 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1033031758 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12509163 RMVar_hsa_circ_93518,RMVar_hsa_circ_171230 7944 RMVar_ID_7944 Human_SNP_ID_575005002 A-to-I Human chr15 - 42544558 42544558 42544558 GCAGCCTCCCAAGGTGCTGGGATTACAGGTGTAAGCCACCACACCCGGCCCTATGTGCTTTATTT GCAGCCTCCCAAGGTGCTGGGATTACAGGTGTTAGCCACCACACCCGGCCCTATGTGCTTTATTT T A LRRC57,AC018362.3 Ensembl:ENSG00000180979,Ensembl:ENSG00000285942 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs756764541 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93518,RMVar_hsa_circ_171230 7945 RMVar_ID_7945 Human_SNP_ID_575005003 A-to-I Human chr15 - 42544558 42544558 42544558 GCAGCCTCCCAAGGTGCTGGGATTACAGGTGTAAGCCACCACACCCGGCCCTATGTGCTTTATTT GCAGCCTCCCAAGGTGCTGGGATTACAGGTGTGAGCCACCACACCCGGCCCTATGTGCTTTATTT T C LRRC57,AC018362.3 Ensembl:ENSG00000180979,Ensembl:ENSG00000285942 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs756764541 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93518,RMVar_hsa_circ_171230 7946 RMVar_ID_7946 Human_SNP_ID_575007080 A-to-I Human chr15 + 42551504 42551504 42551504 CTCTACTACAAATACAAAAATCAGCCGGGTATAGTGGTAGGTGCCTGTAATCCCAGCTACTCGGG CTCTACTACAAATACAAAAATCAGCCGGGTATGGTGGTAGGTGCCTGTAATCCCAGCTACTCGGG A G HAUS2 Ensembl:ENSG00000137814 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1459971136 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12509233 7947 RMVar_ID_7947 Human_SNP_ID_575009302 A-to-I Human chr15 + 42558700 42558700 42558700 CAAAAGTTGGCCAGATGTAGTGGCTCACACCTATAATCCTCGCACTTTGGGAGGCCAAGGTGGGA CAAAAGTTGGCCAGATGTAGTGGCTCACACCTGTAATCCTCGCACTTTGGGAGGCCAAGGTGGGA A G HAUS2 Ensembl:ENSG00000137814 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs918696558 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1353,RMVar_hsa_circ_12733,RMVar_hsa_circ_279456,RMVar_hsa_circ_171231,RMVar_hsa_circ_171232 7948 RMVar_ID_7948 Human_SNP_ID_575010940 A-to-I Human chr15 + 42564899 42564899 42564899 CTCTTGTTGCCCAGGCTGGAGTGCAATGGCACAATCTCGGCTCAGTGCAACCTCCGCCTCTTGGG CTCTTGTTGCCCAGGCTGGAGTGCAATGGCACGATCTCGGCTCAGTGCAACCTCCGCCTCTTGGG A G HAUS2 Ensembl:ENSG00000137814 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs747905002 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_171232 7949 RMVar_ID_7949 Human_SNP_ID_575011549 A-to-I Human chr15 + 42567280 42567280 42567280 AAAATTAGCCGACCATGGTGGTGCATGCCTGTAGTCCCAGCTATTCGGGAGGCTGAGGTAAGAGG AAAATTAGCCGACCATGGTGGTGCATGCCTGTGGTCCCAGCTATTCGGGAGGCTGAGGTAAGAGG A G HAUS2 Ensembl:ENSG00000137814 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1411981383 Functional Loss SNV dbSNP153 33..33 33 - - - 7950 RMVar_ID_7950 Human_SNP_ID_575011556 A-to-I Human chr15 + 42567307 42567307 42567307 CCTGTAGTCCCAGCTATTCGGGAGGCTGAGGTAAGAGGATCACCTAAGCCTGTGAGGTCATGGTT CCTGTAGTCCCAGCTATTCGGGAGGCTGAGGTGAGAGGATCACCTAAGCCTGTGAGGTCATGGTT A G HAUS2 Ensembl:ENSG00000137814 Protein coding 3'UTR GSE38233;GSE99789;GSE107867;GSE107867 cultured B-cells;esophageal squamous carcinoma cells,EC109;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 24183664,29796672,30559470,30559470 RNA-Seq:(High) rs1050320574 Functional Loss SNV dbSNP153 33..33 33 - - - 7951 RMVar_ID_7951 Human_SNP_ID_575011698 A-to-I Human chr15 + 42567885 42567885 42567885 AAAAAATACAAAAATTAGCCAGGCATGGTAGCATGTGCCTGTAATCCCAGCTACTCAGGAGGCTG AAAAAATACAAAAATTAGCCAGGCATGGTAGCGTGTGCCTGTAATCCCAGCTACTCAGGAGGCTG A G HAUS2 Ensembl:ENSG00000137814 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1456429429 Functional Loss SNV dbSNP153 33..33 33 - - - 7952 RMVar_ID_7952 Human_SNP_ID_575012076 A-to-I Human chr15 + 42569436 42569436 42569436 TCAAGTGATCCTCCCACCTCAGCCTCCCAAGTAGCTGGGACTATAGGCACGCGCCACCACGCCTG TCAAGTGATCCTCCCACCTCAGCCTCCCAAGTGGCTGGGACTATAGGCACGCGCCACCACGCCTG A G HAUS2 Ensembl:ENSG00000137814 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1317381656 Functional Loss SNV dbSNP153 33..33 33 - - - 7953 RMVar_ID_7953 Human_SNP_ID_575012078 A-to-I Human chr15 + 42569446 42569444 42569446 CTCCCACCTCAGCCTCCCAAGTAGCTGGGACTATAGGCACGCGCCACCACGCCTGGCTAATTTTT CTCCCACCTCAGCCTCCCAAGTAGCTGGGAC__TAGGCACGCGCCACCACGCCTGGCTAATTTTT CTA C HAUS2 Ensembl:ENSG00000137814 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1325192023 Functional Loss DEL dbSNP153 32..33 33 - - - 7954 RMVar_ID_7954 Human_SNP_ID_575012081 A-to-I Human chr15 + 42569446 42569446 42569446 CTCCCACCTCAGCCTCCCAAGTAGCTGGGACTATAGGCACGCGCCACCACGCCTGGCTAATTTTT CTCCCACCTCAGCCTCCCAAGTAGCTGGGACTGTAGGCACGCGCCACCACGCCTGGCTAATTTTT A G HAUS2 Ensembl:ENSG00000137814 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1217134780 Functional Loss SNV dbSNP153 33..33 33 - - - 7955 RMVar_ID_7955 Human_SNP_ID_575012082 A-to-I Human chr15 + 42569452 42569452 42569452 CCTCAGCCTCCCAAGTAGCTGGGACTATAGGCACGCGCCACCACGCCTGGCTAATTTTTGTATTT CCTCAGCCTCCCAAGTAGCTGGGACTATAGGCGCGCGCCACCACGCCTGGCTAATTTTTGTATTT A G HAUS2 Ensembl:ENSG00000137814 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1411064435 Functional Loss SNV dbSNP153 33..33 33 - - - 7956 RMVar_ID_7956 Human_SNP_ID_575012093 A-to-I Human chr15 + 42569472 42569472 42569472 GGGACTATAGGCACGCGCCACCACGCCTGGCTAATTTTTGTATTTTCTGTAGAGACAGAGTTTTG GGGACTATAGGCACGCGCCACCACGCCTGGCTCATTTTTGTATTTTCTGTAGAGACAGAGTTTTG A C HAUS2 Ensembl:ENSG00000137814 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1196388265 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12509445 7957 RMVar_ID_7957 Human_SNP_ID_575012101 A-to-I Human chr15 + 42569496 42569495 42569497 GCCTGGCTAATTTTTGTATTTTCTGTAGAGACAGAGTTTTGCCATGTTGTTGAGGCTGGTCTTGA GCCTGGCTAATTTTTGTATTTTCTGTAGAGAC__AGTTTTGCCATGTTGTTGAGGCTGGTCTTGA CAG C HAUS2 Ensembl:ENSG00000137814 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1052605644 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_12509446 7958 RMVar_ID_7958 Human_SNP_ID_575012112 A-to-I Human chr15 + 42569559 42569559 42569559 GAACTCCTGGGTTCAAACGACCCTCCCGCCTCAGCCTCCGAAAGTGCTGGGAGTACAGGTGTTAG GAACTCCTGGGTTCAAACGACCCTCCCGCCTCGGCCTCCGAAAGTGCTGGGAGTACAGGTGTTAG A G HAUS2 Ensembl:ENSG00000137814 Protein coding 3'UTR GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs1182650102 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26433947 7959 RMVar_ID_7959 Human_SNP_ID_575012116 A-to-I Human chr15 + 42569568 42569568 42569568 GGTTCAAACGACCCTCCCGCCTCAGCCTCCGAAAGTGCTGGGAGTACAGGTGTTAGCCACTGCGC GGTTCAAACGACCCTCCCGCCTCAGCCTCCGACAGTGCTGGGAGTACAGGTGTTAGCCACTGCGC A C HAUS2 Ensembl:ENSG00000137814 Protein coding 3'UTR GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1205870967 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26437554 7960 RMVar_ID_7960 Human_SNP_ID_575015159 A-to-I Human chr15 - 42581337 42581337 42581337 GACGCTCTTCTCCACCACACCAGGAGAAACTCAAATCATTTATGATAGAAAGTTTCTGTTGGATC GACGCTCTTCTCCACCACACCAGGAGAAACTCCAATCATTTATGATAGAAAGTTTCTGTTGGATC T G EIF4EBP2P2 Ensembl:ENSG00000260282 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs186316269 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5568452 7961 RMVar_ID_7961 Human_SNP_ID_575038269 A-to-I Human chr15 + 42669889 42669889 42669889 CCTGGCCAACATGGTGAAACCCCACCTCTACTAAAAATACAAAAGTTAGCCGGGCGTGGTGGTGG CCTGGCCAACATGGTGAAACCCCACCTCTACTGAAAATACAAAAGTTAGCCGGGCGTGGTGGTGG A G STARD9 Ensembl:ENSG00000159433 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1000182591 Functional Loss SNV dbSNP153 33..33 33 - - - 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 7962 RMVar_ID_7962 Human_SNP_ID_575038609 A-to-I Human chr15 + 42671218 42671218 42671218 GCAGTGGCGCGATCTTAGCTCACTGCAACCTCAACCTCCTGGGCTCAAGTGATTCTCCTGCCTAA GCAGTGGCGCGATCTTAGCTCACTGCAACCTCCACCTCCTGGGCTCAAGTGATTCTCCTGCCTAA A C STARD9 Ensembl:ENSG00000159433 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1328076720 Functional Loss SNV dbSNP153 33..33 33 - - - 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 7963 RMVar_ID_7963 Human_SNP_ID_575038764 A-to-I Human chr15 + 42671839 42671839 42671839 AATTTTTGTGTTTTTAGTAGAGACGGGGATTCACCATGTTGGCCAGGCTGGTCTTGAATTCCTAA AATTTTTGTGTTTTTAGTAGAGACGGGGATTCGCCATGTTGGCCAGGCTGGTCTTGAATTCCTAA A G STARD9 Ensembl:ENSG00000159433 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs557213863 Functional Loss SNV dbSNP153 33..33 33 - - - 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 7964 RMVar_ID_7964 Human_SNP_ID_575038765 A-to-I Human chr15 + 42671842 42671842 42671842 TTTTGTGTTTTTAGTAGAGACGGGGATTCACCATGTTGGCCAGGCTGGTCTTGAATTCCTAACCT TTTTGTGTTTTTAGTAGAGACGGGGATTCACCGTGTTGGCCAGGCTGGTCTTGAATTCCTAACCT A G STARD9 Ensembl:ENSG00000159433 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1235492479 Functional Loss SNV dbSNP153 33..33 33 - - - 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 7965 RMVar_ID_7965 Human_SNP_ID_575038772 A-to-I Human chr15 + 42671870 42671870 42671870 CACCATGTTGGCCAGGCTGGTCTTGAATTCCTAACCTCAAGTGATCCACCCATCTTGGTCTCCTA CACCATGTTGGCCAGGCTGGTCTTGAATTCCTCACCTCAAGTGATCCACCCATCTTGGTCTCCTA A C STARD9 Ensembl:ENSG00000159433 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1188266350 Functional Loss SNV dbSNP153 33..33 33 - - - 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 7966 RMVar_ID_7966 Human_SNP_ID_575038984 A-to-I Human chr15 + 42672888 42672888 42672888 GGGAGGCTGAGGTAGGCAGATCACCTGAGGTGAGGAGTTCGAGACAACCCTGGACAACATGGCGA GGGAGGCTGAGGTAGGCAGATCACCTGAGGTGGGGAGTTCGAGACAACCCTGGACAACATGGCGA A G STARD9 Ensembl:ENSG00000159433 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1566922692 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12509717,Human_RBP_ID_18662689 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 7967 RMVar_ID_7967 Human_SNP_ID_575054031 A-to-I Human chr15 - 42723834 42723834 42723834 GGGCATGGTGGTGTGTGCCTGTAATCCCAGCTACTCAGGAGGATGAGGCAGGAGACCTGCTTGAA GGGCATGGTGGTGTGTGCCTGTAATCCCAGCTGCTCAGGAGGATGAGGCAGGAGACCTGCTTGAA T C CDAN1 Ensembl:ENSG00000140326 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs752891192 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83426,RMVar_hsa_circ_171260 7968 RMVar_ID_7968 Human_SNP_ID_575060140 A-to-I Human chr15 - 42740161 42740161 42740161 CACAGAATATATGTACACTGGCGATGCTGACCATGCCTCCCAGGTACCCTGGCTCTGGGTTCCTT CACAGAATATATGTACACTGGCGATGCTGACCGTGCCTCCCAGGTACCCTGGCTCTGGGTTCCTT T C TTBK2 Ensembl:ENSG00000128881 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs73410961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9052238 7969 RMVar_ID_7969 Human_SNP_ID_575102428 A-to-I Human chr15 - 42915938 42915938 42915938 ACAAAACCTCTGCTTTCTTTCTTTTTTTGGAGACAGGGTCTTGCTCTGTTGCCCAGGCTGGAGTG ACAAAACCTCTGCTTTCTTTCTTTTTTTGGAGCCAGGGTCTTGCTCTGTTGCCCAGGCTGGAGTG T G TTBK2 Ensembl:ENSG00000128881 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1337797672 Functional Loss SNV dbSNP153 33..33 33 - - - 7970 RMVar_ID_7970 Human_SNP_ID_575109439 A-to-I Human chr15 - 42946210 42946210 42946210 TGAGGCAGGAGAATTGCTTGAAACTGGAAGGCAGAGGTTGCCCTGAGCCGTGATCGTACCACGGC TGAGGCAGGAGAATTGCTTGAAACTGGAAGGCGGAGGTTGCCCTGAGCCGTGATCGTACCACGGC T C UBR1 Ensembl:ENSG00000159459 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167939093 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127642,RMVar_hsa_circ_171319 7971 RMVar_ID_7971 Human_SNP_ID_575118509 A-to-I Human chr15 - 42985380 42985380 42985380 CCATTGCACTCCAGCTTGGGCAACAAGAGCGAAAGTCTGTCTCAAAAAAAAAATTGTACCCAAAA CCATTGCACTCCAGCTTGGGCAACAAGAGCGAGAGTCTGTCTCAAAAAAAAAATTGTACCCAAAA T C UBR1 Ensembl:ENSG00000159459 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs141472166 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_123274 RMVar_hsa_circ_75,RMVar_hsa_circ_33019,RMVar_hsa_circ_171324,RMVar_hsa_circ_22298,RMVar_hsa_circ_74071,RMVar_hsa_circ_92284,RMVar_hsa_circ_171322,RMVar_hsa_circ_374380,RMVar_hsa_circ_97564,RMVar_hsa_circ_107762,RMVar_hsa_circ_86839,RMVar_hsa_circ_171326,RMVar_hsa_circ_171325,RMVar_hsa_circ_93039,RMVar_hsa_circ_171323,RMVar_hsa_circ_127576,RMVar_hsa_circ_171333,RMVar_hsa_circ_320558,RMVar_hsa_circ_102048,RMVar_hsa_circ_123970,RMVar_hsa_circ_20702,RMVar_hsa_circ_1441,RMVar_hsa_circ_26064,RMVar_hsa_circ_171343,RMVar_hsa_circ_171334,RMVar_hsa_circ_171336,RMVar_hsa_circ_171337,RMVar_hsa_circ_171335,RMVar_hsa_circ_362232,RMVar_hsa_circ_370694,RMVar_hsa_circ_307106,RMVar_hsa_circ_342836,RMVar_hsa_circ_121930,RMVar_hsa_circ_317559,RMVar_hsa_circ_350471,RMVar_hsa_circ_369792,RMVar_hsa_circ_171342,RMVar_hsa_circ_374485,RMVar_hsa_circ_366675,RMVar_hsa_circ_301799,RMVar_hsa_circ_315078,RMVar_hsa_circ_274495,RMVar_hsa_circ_100176,RMVar_hsa_circ_116212,RMVar_hsa_circ_41620,RMVar_hsa_circ_123252,RMVar_hsa_circ_171346,RMVar_hsa_circ_171350,RMVar_hsa_circ_5319,RMVar_hsa_circ_14587,RMVar_hsa_circ_171352,RMVar_hsa_circ_171351,RMVar_hsa_circ_171348,RMVar_hsa_circ_171349,RMVar_hsa_circ_171347,RMVar_hsa_circ_171344,RMVar_hsa_circ_171345,RMVar_hsa_circ_127950,RMVar_hsa_circ_273378,RMVar_hsa_circ_171354,RMVar_hsa_circ_171355,RMVar_hsa_circ_309975,RMVar_hsa_circ_348532,RMVar_hsa_circ_302507,RMVar_hsa_circ_19658,RMVar_hsa_circ_32418,RMVar_hsa_circ_15122,RMVar_hsa_circ_85012,RMVar_hsa_circ_171356,RMVar_hsa_circ_171357,RMVar_hsa_circ_171358 7972 RMVar_ID_7972 Human_SNP_ID_575118557 A-to-I Human chr15 - 42985577 42985577 42985577 AGGCTGAGGTGGGCGGATCACCTAAGGTCAGAAGTGCGAGACCAGCCTGGCTAACATGCTGAAAC AGGCTGAGGTGGGCGGATCACCTAAGGTCAGAGGTGCGAGACCAGCCTGGCTAACATGCTGAAAC T C UBR1 Ensembl:ENSG00000159459 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1297981923 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75,RMVar_hsa_circ_33019,RMVar_hsa_circ_171324,RMVar_hsa_circ_22298,RMVar_hsa_circ_74071,RMVar_hsa_circ_92284,RMVar_hsa_circ_171322,RMVar_hsa_circ_374380,RMVar_hsa_circ_97564,RMVar_hsa_circ_107762,RMVar_hsa_circ_86839,RMVar_hsa_circ_171326,RMVar_hsa_circ_171325,RMVar_hsa_circ_93039,RMVar_hsa_circ_171323,RMVar_hsa_circ_127576,RMVar_hsa_circ_171333,RMVar_hsa_circ_320558,RMVar_hsa_circ_102048,RMVar_hsa_circ_123970,RMVar_hsa_circ_20702,RMVar_hsa_circ_1441,RMVar_hsa_circ_26064,RMVar_hsa_circ_171343,RMVar_hsa_circ_171334,RMVar_hsa_circ_171336,RMVar_hsa_circ_171337,RMVar_hsa_circ_171335,RMVar_hsa_circ_362232,RMVar_hsa_circ_370694,RMVar_hsa_circ_307106,RMVar_hsa_circ_342836,RMVar_hsa_circ_121930,RMVar_hsa_circ_317559,RMVar_hsa_circ_350471,RMVar_hsa_circ_369792,RMVar_hsa_circ_171342,RMVar_hsa_circ_374485,RMVar_hsa_circ_366675,RMVar_hsa_circ_301799,RMVar_hsa_circ_315078,RMVar_hsa_circ_274495,RMVar_hsa_circ_100176,RMVar_hsa_circ_116212,RMVar_hsa_circ_41620,RMVar_hsa_circ_123252,RMVar_hsa_circ_171346,RMVar_hsa_circ_171350,RMVar_hsa_circ_5319,RMVar_hsa_circ_14587,RMVar_hsa_circ_171352,RMVar_hsa_circ_171351,RMVar_hsa_circ_171348,RMVar_hsa_circ_171349,RMVar_hsa_circ_171347,RMVar_hsa_circ_171344,RMVar_hsa_circ_171345,RMVar_hsa_circ_127950,RMVar_hsa_circ_273378,RMVar_hsa_circ_171354,RMVar_hsa_circ_171355,RMVar_hsa_circ_309975,RMVar_hsa_circ_348532,RMVar_hsa_circ_302507,RMVar_hsa_circ_19658,RMVar_hsa_circ_32418,RMVar_hsa_circ_15122,RMVar_hsa_circ_85012,RMVar_hsa_circ_171356,RMVar_hsa_circ_171357,RMVar_hsa_circ_171358 7973 RMVar_ID_7973 Human_SNP_ID_575118566 A-to-I Human chr15 - 42985626 42985626 42985626 ACCCGAGGTCGGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGAAGGCTGAGGTGGGCGG ACCCGAGGTCGGGCGCAGTGGCTCACGCCTGTCATCCCAGCACTTTGGAAGGCTGAGGTGGGCGG T G UBR1 Ensembl:ENSG00000159459 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1392434935 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6426508 RMVar_hsa_circ_75,RMVar_hsa_circ_33019,RMVar_hsa_circ_171324,RMVar_hsa_circ_22298,RMVar_hsa_circ_74071,RMVar_hsa_circ_92284,RMVar_hsa_circ_171322,RMVar_hsa_circ_374380,RMVar_hsa_circ_97564,RMVar_hsa_circ_107762,RMVar_hsa_circ_86839,RMVar_hsa_circ_171326,RMVar_hsa_circ_171325,RMVar_hsa_circ_93039,RMVar_hsa_circ_171323,RMVar_hsa_circ_127576,RMVar_hsa_circ_171333,RMVar_hsa_circ_320558,RMVar_hsa_circ_102048,RMVar_hsa_circ_123970,RMVar_hsa_circ_20702,RMVar_hsa_circ_1441,RMVar_hsa_circ_26064,RMVar_hsa_circ_171343,RMVar_hsa_circ_171334,RMVar_hsa_circ_171336,RMVar_hsa_circ_171337,RMVar_hsa_circ_171335,RMVar_hsa_circ_362232,RMVar_hsa_circ_370694,RMVar_hsa_circ_307106,RMVar_hsa_circ_342836,RMVar_hsa_circ_121930,RMVar_hsa_circ_317559,RMVar_hsa_circ_350471,RMVar_hsa_circ_369792,RMVar_hsa_circ_171342,RMVar_hsa_circ_374485,RMVar_hsa_circ_366675,RMVar_hsa_circ_301799,RMVar_hsa_circ_315078,RMVar_hsa_circ_274495,RMVar_hsa_circ_100176,RMVar_hsa_circ_116212,RMVar_hsa_circ_41620,RMVar_hsa_circ_123252,RMVar_hsa_circ_171346,RMVar_hsa_circ_171350,RMVar_hsa_circ_5319,RMVar_hsa_circ_14587,RMVar_hsa_circ_171352,RMVar_hsa_circ_171351,RMVar_hsa_circ_171348,RMVar_hsa_circ_171349,RMVar_hsa_circ_171347,RMVar_hsa_circ_171344,RMVar_hsa_circ_171345,RMVar_hsa_circ_127950,RMVar_hsa_circ_273378,RMVar_hsa_circ_171354,RMVar_hsa_circ_171355,RMVar_hsa_circ_309975,RMVar_hsa_circ_348532,RMVar_hsa_circ_302507,RMVar_hsa_circ_19658,RMVar_hsa_circ_32418,RMVar_hsa_circ_15122,RMVar_hsa_circ_85012,RMVar_hsa_circ_171356,RMVar_hsa_circ_171357,RMVar_hsa_circ_171358 7974 RMVar_ID_7974 Human_SNP_ID_575118627 A-to-I Human chr15 - 42985861 42985861 42985861 CCTCAGCCTCCTGAGCAGTTGGGACCATAGGCATGTGCCACCACGCCCAGCTAATTTTTGTGTTT CCTCAGCCTCCTGAGCAGTTGGGACCATAGGCGTGTGCCACCACGCCCAGCTAATTTTTGTGTTT T C UBR1 Ensembl:ENSG00000159459 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs550952939 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75,RMVar_hsa_circ_33019,RMVar_hsa_circ_171324,RMVar_hsa_circ_22298,RMVar_hsa_circ_74071,RMVar_hsa_circ_92284,RMVar_hsa_circ_171322,RMVar_hsa_circ_374380,RMVar_hsa_circ_97564,RMVar_hsa_circ_107762,RMVar_hsa_circ_86839,RMVar_hsa_circ_171326,RMVar_hsa_circ_171325,RMVar_hsa_circ_93039,RMVar_hsa_circ_171323,RMVar_hsa_circ_127576,RMVar_hsa_circ_171333,RMVar_hsa_circ_320558,RMVar_hsa_circ_102048,RMVar_hsa_circ_123970,RMVar_hsa_circ_20702,RMVar_hsa_circ_1441,RMVar_hsa_circ_26064,RMVar_hsa_circ_171343,RMVar_hsa_circ_171334,RMVar_hsa_circ_171336,RMVar_hsa_circ_171337,RMVar_hsa_circ_171335,RMVar_hsa_circ_362232,RMVar_hsa_circ_370694,RMVar_hsa_circ_307106,RMVar_hsa_circ_342836,RMVar_hsa_circ_121930,RMVar_hsa_circ_317559,RMVar_hsa_circ_350471,RMVar_hsa_circ_369792,RMVar_hsa_circ_171342,RMVar_hsa_circ_374485,RMVar_hsa_circ_366675,RMVar_hsa_circ_301799,RMVar_hsa_circ_315078,RMVar_hsa_circ_274495,RMVar_hsa_circ_100176,RMVar_hsa_circ_116212,RMVar_hsa_circ_41620,RMVar_hsa_circ_123252,RMVar_hsa_circ_171346,RMVar_hsa_circ_171350,RMVar_hsa_circ_5319,RMVar_hsa_circ_14587,RMVar_hsa_circ_171352,RMVar_hsa_circ_171351,RMVar_hsa_circ_171348,RMVar_hsa_circ_171349,RMVar_hsa_circ_171347,RMVar_hsa_circ_171344,RMVar_hsa_circ_171345,RMVar_hsa_circ_127950,RMVar_hsa_circ_273378,RMVar_hsa_circ_171354,RMVar_hsa_circ_171355,RMVar_hsa_circ_309975,RMVar_hsa_circ_348532,RMVar_hsa_circ_302507,RMVar_hsa_circ_19658,RMVar_hsa_circ_32418,RMVar_hsa_circ_15122,RMVar_hsa_circ_85012,RMVar_hsa_circ_171356,RMVar_hsa_circ_171357,RMVar_hsa_circ_171358 7975 RMVar_ID_7975 Human_SNP_ID_575121914 A-to-I Human chr15 - 42999645 42999645 42999645 TTTTGTATTTTTTGTAGAGACAGGGTTTCACTATGTTTCCCAGGCTGTTCTCTAACTCCTGGGCT TTTTGTATTTTTTGTAGAGACAGGGTTTCACTGTGTTTCCCAGGCTGTTCTCTAACTCCTGGGCT T C UBR1 Ensembl:ENSG00000159459 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs987985667 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75,RMVar_hsa_circ_33019,RMVar_hsa_circ_171324,RMVar_hsa_circ_22298,RMVar_hsa_circ_74071,RMVar_hsa_circ_374380,RMVar_hsa_circ_86839,RMVar_hsa_circ_171323,RMVar_hsa_circ_127576,RMVar_hsa_circ_102048,RMVar_hsa_circ_123970,RMVar_hsa_circ_20702,RMVar_hsa_circ_1441,RMVar_hsa_circ_26064,RMVar_hsa_circ_171343,RMVar_hsa_circ_171334,RMVar_hsa_circ_171336,RMVar_hsa_circ_171335,RMVar_hsa_circ_370694,RMVar_hsa_circ_307106,RMVar_hsa_circ_121930,RMVar_hsa_circ_317559,RMVar_hsa_circ_350471,RMVar_hsa_circ_369792,RMVar_hsa_circ_374485,RMVar_hsa_circ_366675,RMVar_hsa_circ_301799,RMVar_hsa_circ_100176,RMVar_hsa_circ_116212,RMVar_hsa_circ_41620,RMVar_hsa_circ_123252,RMVar_hsa_circ_171346,RMVar_hsa_circ_171350,RMVar_hsa_circ_5319,RMVar_hsa_circ_14587,RMVar_hsa_circ_171351,RMVar_hsa_circ_171348,RMVar_hsa_circ_171349,RMVar_hsa_circ_171347,RMVar_hsa_circ_171344,RMVar_hsa_circ_171345,RMVar_hsa_circ_127950,RMVar_hsa_circ_171354,RMVar_hsa_circ_171355,RMVar_hsa_circ_309975,RMVar_hsa_circ_348532,RMVar_hsa_circ_19658,RMVar_hsa_circ_32418,RMVar_hsa_circ_15122,RMVar_hsa_circ_13663,RMVar_hsa_circ_85012,RMVar_hsa_circ_171357,RMVar_hsa_circ_171358,RMVar_hsa_circ_329820,RMVar_hsa_circ_300369,RMVar_hsa_circ_268396,RMVar_hsa_circ_293029,RMVar_hsa_circ_68803,RMVar_hsa_circ_171359,RMVar_hsa_circ_171361,RMVar_hsa_circ_171363,RMVar_hsa_circ_171362,RMVar_hsa_circ_171360,RMVar_hsa_circ_171366,RMVar_hsa_circ_94597,RMVar_hsa_circ_284177,RMVar_hsa_circ_344455,RMVar_hsa_circ_376483,RMVar_hsa_circ_305777,RMVar_hsa_circ_275589,RMVar_hsa_circ_171367,RMVar_hsa_circ_171365 7976 RMVar_ID_7976 Human_SNP_ID_575164203 A-to-I Human chr15 + 43171291 43171291 43171291 TTGGGAGGCAGAGGTTGCAGTGAGCCGAGATCATGTCACTGCACTCCAGCTTGGGCAACAGAGCG TTGGGAGGCAGAGGTTGCAGTGAGCCGAGATCCTGTCACTGCACTCCAGCTTGGGCAACAGAGCG A C TMEM62 Ensembl:ENSG00000137842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs977126779 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49270,RMVar_hsa_circ_86603,RMVar_hsa_circ_37940,RMVar_hsa_circ_47235,RMVar_hsa_circ_171411,RMVar_hsa_circ_47211,RMVar_hsa_circ_331912,RMVar_hsa_circ_47460,RMVar_hsa_circ_64395 7977 RMVar_ID_7977 Human_SNP_ID_575164204 A-to-I Human chr15 + 43171291 43171291 43171291 TTGGGAGGCAGAGGTTGCAGTGAGCCGAGATCATGTCACTGCACTCCAGCTTGGGCAACAGAGCG TTGGGAGGCAGAGGTTGCAGTGAGCCGAGATCGTGTCACTGCACTCCAGCTTGGGCAACAGAGCG A G TMEM62 Ensembl:ENSG00000137842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs977126779 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49270,RMVar_hsa_circ_86603,RMVar_hsa_circ_37940,RMVar_hsa_circ_47235,RMVar_hsa_circ_171411,RMVar_hsa_circ_47211,RMVar_hsa_circ_331912,RMVar_hsa_circ_47460,RMVar_hsa_circ_64395 7978 RMVar_ID_7978 Human_SNP_ID_575168298 A-to-I Human chr15 + 43188906 43188906 43188906 CGAGACCAGTGTGGCCAGTGTGGCAAAACCCCATCTCTACTAAAAATACAAAAAATTAGCTGGGT CGAGACCAGTGTGGCCAGTGTGGCAAAACCCCGTCTCTACTAAAAATACAAAAAATTAGCTGGGT A G CCNDBP1 Ensembl:ENSG00000166946 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1457441744 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26537,RMVar_hsa_circ_171424 7979 RMVar_ID_7979 Human_SNP_ID_575168338 A-to-I Human chr15 + 43189043 43189043 43189043 GAGGTTGCAGTGAGCCAAGATTGCGCCATTGCACTCCAGCCTGGGTGACAGAGTGAGACTCTGTC GAGGTTGCAGTGAGCCAAGATTGCGCCATTGCCCTCCAGCCTGGGTGACAGAGTGAGACTCTGTC A C CCNDBP1 Ensembl:ENSG00000166946 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs572239852 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26537,RMVar_hsa_circ_171424 7980 RMVar_ID_7980 Human_SNP_ID_575168339 A-to-I Human chr15 + 43189043 43189043 43189043 GAGGTTGCAGTGAGCCAAGATTGCGCCATTGCACTCCAGCCTGGGTGACAGAGTGAGACTCTGTC GAGGTTGCAGTGAGCCAAGATTGCGCCATTGCGCTCCAGCCTGGGTGACAGAGTGAGACTCTGTC A G CCNDBP1 Ensembl:ENSG00000166946 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs572239852 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26537,RMVar_hsa_circ_171424 7981 RMVar_ID_7981 Human_SNP_ID_575209063 A-to-I Human chr15 + 43352968 43352968 43352968 AGCTGCAGCTCTCTTTTTTTTTTTTTTCAACAAAGGCTCTCACTCTGTTCCCCAGGCTGGAGTGC AGCTGCAGCTCTCTTTTTTTTTTTTTTCAACAGAGGCTCTCACTCTGTTCCCCAGGCTGGAGTGC A G ADAL Ensembl:ENSG00000168803 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs370805359 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6426887,Human_RBP_ID_26433976 RMVar_hsa_circ_89242,RMVar_hsa_circ_171434 7982 RMVar_ID_7982 Human_SNP_ID_575218206 A-to-I Human chr15 + 43387926 43387926 43387926 GCTGAAGTGCAGTGGAGCAGTCGCGGCTCACTACAAACTCCGCCTCCCGGGTTGAAGCAATTCAC GCTGAAGTGCAGTGGAGCAGTCGCGGCTCACTCCAAACTCCGCCTCCCGGGTTGAAGCAATTCAC A C TUBGCP4 Ensembl:ENSG00000137822 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs919897249 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88554,RMVar_hsa_circ_339561,RMVar_hsa_circ_110580,RMVar_hsa_circ_171444,RMVar_hsa_circ_171445,RMVar_hsa_circ_171450,RMVar_hsa_circ_365307,RMVar_hsa_circ_171452,RMVar_hsa_circ_171453,RMVar_hsa_circ_375915,RMVar_hsa_circ_373328,RMVar_hsa_circ_171454,RMVar_hsa_circ_171455,RMVar_hsa_circ_104193 7983 RMVar_ID_7983 Human_SNP_ID_575218207 A-to-I Human chr15 + 43387926 43387926 43387926 GCTGAAGTGCAGTGGAGCAGTCGCGGCTCACTACAAACTCCGCCTCCCGGGTTGAAGCAATTCAC GCTGAAGTGCAGTGGAGCAGTCGCGGCTCACTGCAAACTCCGCCTCCCGGGTTGAAGCAATTCAC A G TUBGCP4 Ensembl:ENSG00000137822 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs919897249 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88554,RMVar_hsa_circ_339561,RMVar_hsa_circ_110580,RMVar_hsa_circ_171444,RMVar_hsa_circ_171445,RMVar_hsa_circ_171450,RMVar_hsa_circ_365307,RMVar_hsa_circ_171452,RMVar_hsa_circ_171453,RMVar_hsa_circ_375915,RMVar_hsa_circ_373328,RMVar_hsa_circ_171454,RMVar_hsa_circ_171455,RMVar_hsa_circ_104193 7984 RMVar_ID_7984 Human_SNP_ID_575219116 A-to-I Human chr15 + 43391999 43391999 43391999 ATTGCTTGAACCTCGGAGGCAGAGGTTGCAGCAAGCTGAGATGGTGCCACTGCATTCCAGCCTGG ATTGCTTGAACCTCGGAGGCAGAGGTTGCAGCCAGCTGAGATGGTGCCACTGCATTCCAGCCTGG A C TUBGCP4 Ensembl:ENSG00000137822 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909185056 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88554,RMVar_hsa_circ_339561,RMVar_hsa_circ_110580,RMVar_hsa_circ_171444,RMVar_hsa_circ_171445,RMVar_hsa_circ_171450,RMVar_hsa_circ_365307,RMVar_hsa_circ_171452,RMVar_hsa_circ_171453,RMVar_hsa_circ_375915,RMVar_hsa_circ_373328,RMVar_hsa_circ_171454,RMVar_hsa_circ_171455,RMVar_hsa_circ_104193 7985 RMVar_ID_7985 Human_SNP_ID_575221348 A-to-I Human chr15 + 43400448 43400448 43400448 GAGACAGGGTCTTTCTCTGTTTCCCAGGCTGGAATGCAGTGGTACAGTCATAGCTCACTGAAGCC GAGACAGGGTCTTTCTCTGTTTCCCAGGCTGGCATGCAGTGGTACAGTCATAGCTCACTGAAGCC A C TUBGCP4 Ensembl:ENSG00000137822 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs987880601 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88554,RMVar_hsa_circ_110580,RMVar_hsa_circ_171445,RMVar_hsa_circ_22718,RMVar_hsa_circ_171450,RMVar_hsa_circ_365307,RMVar_hsa_circ_171452,RMVar_hsa_circ_373328,RMVar_hsa_circ_171454,RMVar_hsa_circ_171455,RMVar_hsa_circ_104193,RMVar_hsa_circ_273259,RMVar_hsa_circ_62632,RMVar_hsa_circ_171456,RMVar_hsa_circ_373827,RMVar_hsa_circ_171457,RMVar_hsa_circ_286810,RMVar_hsa_circ_171459,RMVar_hsa_circ_291432,RMVar_hsa_circ_171461,RMVar_hsa_circ_374302,RMVar_hsa_circ_289362,RMVar_hsa_circ_171462,RMVar_hsa_circ_171464,RMVar_hsa_circ_290240,RMVar_hsa_circ_171463 7986 RMVar_ID_7986 Human_SNP_ID_575244202 A-to-I Human chr15 - 43486214 43486214 43486214 GTGCCACCATGCCCGGCTAATTTTGTATTTTTAGTGGAGATAGGGTTTCTCCATGTTCGTCAGGC GTGCCACCATGCCCGGCTAATTTTGTATTTTTCGTGGAGATAGGGTTTCTCCATGTTCGTCAGGC T G TP53BP1 Ensembl:ENSG00000067369 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1159911916 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_889,RMVar_hsa_circ_171468,RMVar_hsa_circ_52051 7987 RMVar_ID_7987 Human_SNP_ID_575245114 A-to-I Human chr15 - 43490015 43490015 43490015 CCAGCTATTCAGGAGACTGAGATAGAAGGATCACTTGAGCCTGGAAGATTGAGGCTGCAGTCAGC CCAGCTATTCAGGAGACTGAGATAGAAGGATCGCTTGAGCCTGGAAGATTGAGGCTGCAGTCAGC T C TP53BP1 Ensembl:ENSG00000067369 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1183341710 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12512937 RMVar_hsa_circ_889,RMVar_hsa_circ_171468,RMVar_hsa_circ_52051 7988 RMVar_ID_7988 Human_SNP_ID_575252699 A-to-I Human chr15 + 43520639 43520639 43520639 ATTCTCAATATAAATTCCTACATCTCTCCCTCAGGCCAGAGGACCCTTTGCCACCAGAGTGAGAT ATTCTCAATATAAATTCCTACATCTCTCCCTCCGGCCAGAGGACCCTTTGCCACCAGAGTGAGAT A C MAP1A Ensembl:ENSG00000166963 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1566976749 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4343514 Human_Splice_Rec_1593045,Human_Splice_Rec_1593055 RMVar_hsa_circ_112964,RMVar_hsa_circ_96924,RMVar_hsa_circ_171501 7989 RMVar_ID_7989 Human_SNP_ID_575258890 A-to-I Human chr15 - 43542412 43542412 43542412 TGCTATGCGCCTGTAGTCTGAGCTACTCAGGAAGCTGAGGTTGGAGGATCGCTTGAACCTGGGAG TGCTATGCGCCTGTAGTCTGAGCTACTCAGGACGCTGAGGTTGGAGGATCGCTTGAACCTGGGAG T G PPIP5K1 Ensembl:ENSG00000168781 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1322050962 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6074,RMVar_hsa_circ_98294,RMVar_hsa_circ_100077,RMVar_hsa_circ_171507,RMVar_hsa_circ_76194,RMVar_hsa_circ_171508,RMVar_hsa_circ_171506 7990 RMVar_ID_7990 Human_SNP_ID_575259902 A-to-I Human chr15 - 43546781 43546781 43546781 ATGGTGGTGCACACCTGTAGTCCCAGCTACTCAGGAGACTGAGGTGGAAGAATCACCTGAGCCCC ATGGTGGTGCACACCTGTAGTCCCAGCTACTCCGGAGACTGAGGTGGAAGAATCACCTGAGCCCC T G PPIP5K1 Ensembl:ENSG00000168781 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1411864532 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6074,RMVar_hsa_circ_98294,RMVar_hsa_circ_100077,RMVar_hsa_circ_171507,RMVar_hsa_circ_76194,RMVar_hsa_circ_171508,RMVar_hsa_circ_171506 7991 RMVar_ID_7991 Human_SNP_ID_575260764 A-to-I Human chr15 - 43549957 43549957 43549957 TATAAAGTAATTTTTTGCTGAGATAGGGTCTTATTCTGTCACCCAGGCTTGAGTGTAGTTGTGCC TATAAAGTAATTTTTTGCTGAGATAGGGTCTTGTTCTGTCACCCAGGCTTGAGTGTAGTTGTGCC T C PPIP5K1 Ensembl:ENSG00000168781 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1303221483 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6074,RMVar_hsa_circ_98294,RMVar_hsa_circ_100077,RMVar_hsa_circ_171507,RMVar_hsa_circ_76194,RMVar_hsa_circ_171508,RMVar_hsa_circ_171506 7992 RMVar_ID_7992 Human_SNP_ID_575261433 A-to-I Human chr15 - 43552455 43552455 43552455 GAGATCTGCTGGCTTCGGTCTCCCAAAATGCTAGGATTACAGGCATGAGCCACTGCGCCCAGCCA GAGATCTGCTGGCTTCGGTCTCCCAAAATGCTTGGATTACAGGCATGAGCCACTGCGCCCAGCCA T A PPIP5K1 Ensembl:ENSG00000168781 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1381692459 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25139925 RMVar_hsa_circ_6074,RMVar_hsa_circ_98294,RMVar_hsa_circ_100077,RMVar_hsa_circ_171507,RMVar_hsa_circ_76194,RMVar_hsa_circ_171508,RMVar_hsa_circ_171506 7993 RMVar_ID_7993 Human_SNP_ID_575261434 A-to-I Human chr15 - 43552455 43552455 43552455 GAGATCTGCTGGCTTCGGTCTCCCAAAATGCTAGGATTACAGGCATGAGCCACTGCGCCCAGCCA GAGATCTGCTGGCTTCGGTCTCCCAAAATGCTGGGATTACAGGCATGAGCCACTGCGCCCAGCCA T C PPIP5K1 Ensembl:ENSG00000168781 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1381692459 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25139925 RMVar_hsa_circ_6074,RMVar_hsa_circ_98294,RMVar_hsa_circ_100077,RMVar_hsa_circ_171507,RMVar_hsa_circ_76194,RMVar_hsa_circ_171508,RMVar_hsa_circ_171506 7994 RMVar_ID_7994 Human_SNP_ID_575274561 A-to-I Human chr15 - 43633404 43633404 43633404 TGCTGGGAAATGAAGTCAGAGAGAGAATGGTGACCTGATCCTGTAGGGTTATGGGTGCCATTGTA TGCTGGGAAATGAAGTCAGAGAGAGAATGGTGGCCTGATCCTGTAGGGTTATGGGTGCCATTGTA T C CATSPER2 Ensembl:ENSG00000166762 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs547705367 Functional Loss SNV dbSNP153 33..33 33 - - - 7995 RMVar_ID_7995 Human_SNP_ID_575274825 A-to-I Human chr15 - 43634432 43634432 43634432 GTGGGCAGATGACTTGAGCTCAGGAGTTCGAGACTAAACTAGGCAATATGGTAAAATCCTGTCTC GTGGGCAGATGACTTGAGCTCAGGAGTTCGAGGCTAAACTAGGCAATATGGTAAAATCCTGTCTC T C CATSPER2 Ensembl:ENSG00000166762 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1238499356 Functional Loss SNV dbSNP153 33..33 33 - - - 7996 RMVar_ID_7996 Human_SNP_ID_575277286 A-to-I Human chr15 - 43643355 43643350 43643355 AGAGTGAGTGGGAATCCATCTCAAAAAAAAAAAGAAAGAAATTATGTTTCAACATCAGTATTCCT AGAGTGAGTGGGAATCCATCTCAAAAAAAAAA_____GAAATTATGTTTCAACATCAGTATTCCT CTTTCT C CATSPER2 Ensembl:ENSG00000166762 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1271446779 Functional Loss DEL dbSNP153 33..37 33 - - - Human_RBP_ID_25140035 RMVar_hsa_circ_171526,RMVar_hsa_circ_97014 7997 RMVar_ID_7997 Human_SNP_ID_575277288 A-to-I Human chr15 - 43643355 43643354 43643355 AGAGTGAGTGGGAATCCATCTCAAAAAAAAAAAGAAAGAAATTATGTTTCAACATCAGTATTCCT AGAGTGAGTGGGAATCCATCTCAAAAAAAAAA_GAAAGAAATTATGTTTCAACATCAGTATTCCT CT C CATSPER2 Ensembl:ENSG00000166762 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs955447618 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_25140035 RMVar_hsa_circ_171526,RMVar_hsa_circ_97014 7998 RMVar_ID_7998 Human_SNP_ID_575277775 A-to-I Human chr15 - 43645101 43645101 43645101 CAGTGAGCCATCATGCAACGGAACTCCAGCCTAGGTGACAAAGTGAGACCCTGTCTCAAAAAAAT CAGTGAGCCATCATGCAACGGAACTCCAGCCTGGGTGACAAAGTGAGACCCTGTCTCAAAAAAAT T C CATSPER2 Ensembl:ENSG00000166762 Protein coding intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1238910120 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23307151 RMVar_hsa_circ_171526,RMVar_hsa_circ_97014 7999 RMVar_ID_7999 Human_SNP_ID_575278286 A-to-I Human chr15 - 43646996 43646996 43646996 AAGAGGAAGTGAGGCCGGGCACGCCGGCTCACACGTGTAATCCTAGCACTTTGGGAGGCCGGGGC AAGAGGAAGTGAGGCCGGGCACGCCGGCTCACGCGTGTAATCCTAGCACTTTGGGAGGCCGGGGC T C CATSPER2 Ensembl:ENSG00000166762 Protein coding intron GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line - 24183664,31158229 RNA-Seq:(High) rs1427237458 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_171526,RMVar_hsa_circ_97014 8000 RMVar_ID_8000 Human_SNP_ID_575281610 A-to-I Human chr15 - 43657571 43657571 43657571 AAAAATTAGCCGGGCATTGTGGCGGGCCTGTAATCTCAGCTACTTGGGAGGCTGAGGCAGGGGAA AAAAATTAGCCGGGCATTGTGGCGGGCCTGTAGTCTCAGCTACTTGGGAGGCTGAGGCAGGGGAA T C CATSPER2 Ensembl:ENSG00000166762 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1343781991 Functional Loss SNV dbSNP153 33..33 33 - - - 8001 RMVar_ID_8001 Human_SNP_ID_575292345 A-to-I Human chr15 - 43730946 43730946 43730946 ATTTAGCAGGGTGGGCATGGGCACTCATGCCTATAATACCAGCATTTTCGAAAACTGAGGTGGGC ATTTAGCAGGGTGGGCATGGGCACTCATGCCTGTAATACCAGCATTTTCGAAAACTGAGGTGGGC T C CATSPER2P1 Ensembl:ENSG00000205771 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1038594973 Functional Loss SNV dbSNP153 33..33 33 - - - 8002 RMVar_ID_8002 Human_SNP_ID_575294317 A-to-I Human chr15 - 43739614 43739614 43739614 ACAAGAATCAGTGGGTATGGTGATGTGCACCTATGGTTCCAGTTACTCAGGAGGCTGAGGCAGAA ACAAGAATCAGTGGGTATGGTGATGTGCACCTGTGGTTCCAGTTACTCAGGAGGCTGAGGCAGAA T C CATSPER2P1 Ensembl:ENSG00000205771 Pseudogene intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1282984019 Functional Loss SNV dbSNP153 33..33 33 - - - 8003 RMVar_ID_8003 Human_SNP_ID_575294318 A-to-I Human chr15 - 43739614 43739614 43739614 ACAAGAATCAGTGGGTATGGTGATGTGCACCTATGGTTCCAGTTACTCAGGAGGCTGAGGCAGAA ACAAGAATCAGTGGGTATGGTGATGTGCACCTCTGGTTCCAGTTACTCAGGAGGCTGAGGCAGAA T G CATSPER2P1 Ensembl:ENSG00000205771 Pseudogene intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1282984019 Functional Loss SNV dbSNP153 33..33 33 - - - 8004 RMVar_ID_8004 Human_SNP_ID_575294324 A-to-I Human chr15 - 43739637 43739637 43739637 GAAACCCCATCTCTACTAAAAATACAAGAATCAGTGGGTATGGTGATGTGCACCTATGGTTCCAG GAAACCCCATCTCTACTAAAAATACAAGAATCTGTGGGTATGGTGATGTGCACCTATGGTTCCAG T A CATSPER2P1 Ensembl:ENSG00000205771 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs997648922 Functional Loss SNV dbSNP153 33..33 33 - - - 8005 RMVar_ID_8005 Human_SNP_ID_575294325 A-to-I Human chr15 - 43739637 43739637 43739637 GAAACCCCATCTCTACTAAAAATACAAGAATCAGTGGGTATGGTGATGTGCACCTATGGTTCCAG GAAACCCCATCTCTACTAAAAATACAAGAATCGGTGGGTATGGTGATGTGCACCTATGGTTCCAG T C CATSPER2P1 Ensembl:ENSG00000205771 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs997648922 Functional Loss SNV dbSNP153 33..33 33 - - - 8006 RMVar_ID_8006 Human_SNP_ID_575294335 A-to-I Human chr15 - 43739666 43739666 43739666 GAGTTCAAGACCAACCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAGAATCAGTG GAGTTCAAGACCAACCTGGCCAACATGGTGAATCCCCATCTCTACTAAAAATACAAGAATCAGTG T A CATSPER2P1 Ensembl:ENSG00000205771 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1490807318 Functional Loss SNV dbSNP153 33..33 33 - - - 8007 RMVar_ID_8007 Human_SNP_ID_575294336 A-to-I Human chr15 - 43739666 43739666 43739666 GAGTTCAAGACCAACCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAGAATCAGTG GAGTTCAAGACCAACCTGGCCAACATGGTGAACCCCCATCTCTACTAAAAATACAAGAATCAGTG T G CATSPER2P1 Ensembl:ENSG00000205771 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1490807318 Functional Loss SNV dbSNP153 33..33 33 - - - 8008 RMVar_ID_8008 Human_SNP_ID_575294380 A-to-I Human chr15 - 43739838 43739838 43739838 CGCCCGCCTCGGCCTCCCAAAGAGCTGGGATTACAGGCATGAGCCACCGCGCCCAGCCAGAATTA CGCCCGCCTCGGCCTCCCAAAGAGCTGGGATTCCAGGCATGAGCCACCGCGCCCAGCCAGAATTA T G CATSPER2P1 Ensembl:ENSG00000205771 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1404611412 Functional Loss SNV dbSNP153 33..33 33 - - - 8009 RMVar_ID_8009 Human_SNP_ID_575294540 A-to-I Human chr15 - 43740398 43740398 43740398 ATATTAGGAGGGTGAGGTGGGAGGATCACTTGAGCCCAGGGGATTGAGGCAGCAGTGAGCTATGA ATATTAGGAGGGTGAGGTGGGAGGATCACTTGCGCCCAGGGGATTGAGGCAGCAGTGAGCTATGA T G CATSPER2P1 Ensembl:ENSG00000205771 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1171272310 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17563627 8010 RMVar_ID_8010 Human_SNP_ID_575294626 A-to-I Human chr15 - 43740708 43740708 43740708 GCCATCACACCTGGCTAATTTTGTGTATTTTTAGTAGTGATGGGGTTTCACTGTGTTAGCCAGGA GCCATCACACCTGGCTAATTTTGTGTATTTTTGGTAGTGATGGGGTTTCACTGTGTTAGCCAGGA T C CATSPER2P1 Ensembl:ENSG00000205771 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1288243175 Functional Loss SNV dbSNP153 33..33 33 - - - 8011 RMVar_ID_8011 Human_SNP_ID_575294627 A-to-I Human chr15 - 43740708 43740708 43740708 GCCATCACACCTGGCTAATTTTGTGTATTTTTAGTAGTGATGGGGTTTCACTGTGTTAGCCAGGA GCCATCACACCTGGCTAATTTTGTGTATTTTTCGTAGTGATGGGGTTTCACTGTGTTAGCCAGGA T G CATSPER2P1 Ensembl:ENSG00000205771 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1288243175 Functional Loss SNV dbSNP153 33..33 33 - - - 8012 RMVar_ID_8012 Human_SNP_ID_575294924 A-to-I Human chr15 - 43741999 43741999 43741999 CCTCATCTCTACAAAAAATACAAAAATTAGCTAGGTGTGGTGGCACATGCCTGTAGTCCCAGCTA CCTCATCTCTACAAAAAATACAAAAATTAGCTGGGTGTGGTGGCACATGCCTGTAGTCCCAGCTA T C CATSPER2P1 Ensembl:ENSG00000205771 Pseudogene intron GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line - 24183664,31158229 RNA-Seq:(High) rs967567326 Functional Loss SNV dbSNP153 33..33 33 - - - 8013 RMVar_ID_8013 Human_SNP_ID_575294943 A-to-I Human chr15 - 43742085 43742085 43742085 CCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGAGGATTGCTTGAGCTCAGGAGTTTGAGACC CCTGTAATCCCAGCACTTTGGGAGGCTGAGGCTGGAGGATTGCTTGAGCTCAGGAGTTTGAGACC T A CATSPER2P1 Ensembl:ENSG00000205771 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs915997998 Functional Loss SNV dbSNP153 33..33 33 - - - 8014 RMVar_ID_8014 Human_SNP_ID_575294944 A-to-I Human chr15 - 43742085 43742085 43742085 CCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGAGGATTGCTTGAGCTCAGGAGTTTGAGACC CCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGAGGATTGCTTGAGCTCAGGAGTTTGAGACC T C CATSPER2P1 Ensembl:ENSG00000205771 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs915997998 Functional Loss SNV dbSNP153 33..33 33 - - - 8015 RMVar_ID_8015 Human_SNP_ID_575294953 A-to-I Human chr15 - 43742120 43742120 43742120 AGCTTATCTCTGGGGCCCAGGCATGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAG AGCTTATCTCTGGGGCCCAGGCATGGTGGCTCGTGCCTGTAATCCCAGCACTTTGGGAGGCTGAG T C CATSPER2P1 Ensembl:ENSG00000205771 Pseudogene intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1158507241 Functional Loss SNV dbSNP153 33..33 33 - - - 8016 RMVar_ID_8016 Human_SNP_ID_575295035 A-to-I Human chr15 - 43742453 43742453 43742453 CTCCCACGTCAGCCTCCTGAGTAGCTTGGACTACAGGTGCATGCCACTACACCAAGCTAATTATG CTCCCACGTCAGCCTCCTGAGTAGCTTGGACTCCAGGTGCATGCCACTACACCAAGCTAATTATG T G CATSPER2P1 Ensembl:ENSG00000205771 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1180461789 Functional Loss SNV dbSNP153 33..33 33 - - - 8017 RMVar_ID_8017 Human_SNP_ID_575295153 A-to-I Human chr15 - 43742904 43742904 43742904 CACCCGCCTCGGCCTCCCAGAGTGCTGGGATTACAGGGGTGAGCCACTGCGCCCAGCCTAACATT CACCCGCCTCGGCCTCCCAGAGTGCTGGGATTTCAGGGGTGAGCCACTGCGCCCAGCCTAACATT T A CATSPER2P1 Ensembl:ENSG00000205771 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs774011113 Functional Loss SNV dbSNP153 33..33 33 - - - 8018 RMVar_ID_8018 Human_SNP_ID_575295450 A-to-I Human chr15 - 43743909 43743909 43743909 GGGAGGCTGAGGCAGGAGAATCGCTTGAACCCAGGAGGCGTAGGTTTCAGTGAGCTGAGATTGTG GGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGGGAGGCGTAGGTTTCAGTGAGCTGAGATTGTG T C CATSPER2P1 Ensembl:ENSG00000205771 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1408310601 Functional Loss SNV dbSNP153 33..33 33 - - - 8019 RMVar_ID_8019 Human_SNP_ID_575295455 A-to-I Human chr15 - 43743945 43743945 43743945 TGGGCGTGGTGGCATGGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAA TGGGCGTGGTGGCATGGCCTGTAGTCCCAGCTGCTCGGGAGGCTGAGGCAGGAGAATCGCTTGAA T C CATSPER2P1 Ensembl:ENSG00000205771 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs911473745 Functional Loss SNV dbSNP153 33..33 33 - - - 8020 RMVar_ID_8020 Human_SNP_ID_575296898 A-to-I Human chr15 + 43748371 43748371 43748371 ATAGTGGCACATGCCTGTAATCCCAGCTACTCAGGAAGCTGAGGCAGGAGAATAGCTTGAACCCA ATAGTGGCACATGCCTGTAATCCCAGCTACTCGGGAAGCTGAGGCAGGAGAATAGCTTGAACCCA A G PDIA3 Ensembl:ENSG00000167004 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1023388466 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_171531,RMVar_hsa_circ_114800,RMVar_hsa_circ_124137,RMVar_hsa_circ_171532 8021 RMVar_ID_8021 Human_SNP_ID_575297134 A-to-I Human chr15 + 43749173 43749173 43749173 TGGAGTGCAGTGGCATGGTCTGGGCTCACTGCAACCTCCGCCTCCCGTGTTCAAGTGATTCTCCT TGGAGTGCAGTGGCATGGTCTGGGCTCACTGCGACCTCCGCCTCCCGTGTTCAAGTGATTCTCCT A G PDIA3 Ensembl:ENSG00000167004 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1345819012 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_171531,RMVar_hsa_circ_114800,RMVar_hsa_circ_124137,RMVar_hsa_circ_171532 8022 RMVar_ID_8022 Human_SNP_ID_575297149 A-to-I Human chr15 + 43749211 43749211 43749211 CGCCTCCCGTGTTCAAGTGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCACGCA CGCCTCCCGTGTTCAAGTGATTCTCCTGCCTCTGCCTCCTGAGTAGCTGGGATTACAGGCACGCA A T PDIA3 Ensembl:ENSG00000167004 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1398911432 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_171531,RMVar_hsa_circ_114800,RMVar_hsa_circ_124137,RMVar_hsa_circ_171532 8023 RMVar_ID_8023 Human_SNP_ID_575297162 A-to-I Human chr15 + 43749233 43749233 43749233 CTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCACGCACCACCAAGCCCGGCTAATTTTT CTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTGCAGGCACGCACCACCAAGCCCGGCTAATTTTT A G PDIA3 Ensembl:ENSG00000167004 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs779882119 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_171531,RMVar_hsa_circ_114800,RMVar_hsa_circ_124137,RMVar_hsa_circ_171532 8024 RMVar_ID_8024 Human_SNP_ID_575297189 A-to-I Human chr15 + 43749298 43749298 43749298 GTATTTTAGTAGAGACGGGGTTTCACCATGTTAGCCTGATGGTGAACTCCTGACCTCAGGAGATC GTATTTTAGTAGAGACGGGGTTTCACCATGTTCGCCTGATGGTGAACTCCTGACCTCAGGAGATC A C PDIA3 Ensembl:ENSG00000167004 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1441520218 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_171531,RMVar_hsa_circ_114800,RMVar_hsa_circ_124137,RMVar_hsa_circ_171532 8025 RMVar_ID_8025 Human_SNP_ID_575297190 A-to-I Human chr15 + 43749298 43749298 43749298 GTATTTTAGTAGAGACGGGGTTTCACCATGTTAGCCTGATGGTGAACTCCTGACCTCAGGAGATC GTATTTTAGTAGAGACGGGGTTTCACCATGTTTGCCTGATGGTGAACTCCTGACCTCAGGAGATC A T PDIA3 Ensembl:ENSG00000167004 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1441520218 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_171531,RMVar_hsa_circ_114800,RMVar_hsa_circ_124137,RMVar_hsa_circ_171532 8026 RMVar_ID_8026 Human_SNP_ID_575297193 A-to-I Human chr15 + 43749304 43749304 43749304 TAGTAGAGACGGGGTTTCACCATGTTAGCCTGATGGTGAACTCCTGACCTCAGGAGATCCACCCT TAGTAGAGACGGGGTTTCACCATGTTAGCCTGTTGGTGAACTCCTGACCTCAGGAGATCCACCCT A T PDIA3 Ensembl:ENSG00000167004 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1303006188 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_171531,RMVar_hsa_circ_114800,RMVar_hsa_circ_124137,RMVar_hsa_circ_171532 8027 RMVar_ID_8027 Human_SNP_ID_575300116 A-to-I Human chr15 + 43760270 43760270 43760270 AAAACTAGCCAGGTGGGATGGTGCATGCCTGTAGACCCAGCTACTCAGGAGACTGAGGCGAGAGG AAAACTAGCCAGGTGGGATGGTGCATGCCTGTGGACCCAGCTACTCAGGAGACTGAGGCGAGAGG A G PDIA3 Ensembl:ENSG00000167004 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs925965825 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17563367 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_285307,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_171536,RMVar_hsa_circ_171537,RMVar_hsa_circ_171538 8028 RMVar_ID_8028 Human_SNP_ID_575314662 A-to-I Human chr15 - 43808476 43808476 43808476 GAAAGTCCTTTGGTGGGCCAGGTACATTGGCTAATGCCTGTAATCTTAACATTTTGGGAGGCAAG GAAAGTCCTTTGGTGGGCCAGGTACATTGGCTGATGCCTGTAATCTTAACATTTTGGGAGGCAAG T C MFAP1 Ensembl:ENSG00000140259 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs879566033 Functional Loss SNV dbSNP153 33..33 33 - - - 8029 RMVar_ID_8029 Human_SNP_ID_575315303 A-to-I Human chr15 - 43810905 43810905 43810905 TAAAAATACAAAAATTAGTCGGGCATGGTGGCACACACCTGTAATCCCAGCTACTCAGGAGGCTG TAAAAATACAAAAATTAGTCGGGCATGGTGGCGCACACCTGTAATCCCAGCTACTCAGGAGGCTG T C MFAP1 Ensembl:ENSG00000140259 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs34158502 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3164,RMVar_hsa_circ_267845,RMVar_hsa_circ_378570 8030 RMVar_ID_8030 Human_SNP_ID_575315406 A-to-I Human chr15 - 43811287 43811287 43811287 CCTCAGCCTCCTGCGTAGCTGGGACTACAGGTATATGCCACCACGCCCAGCTAATTTTTGTATTT CCTCAGCCTCCTGCGTAGCTGGGACTACAGGTGTATGCCACCACGCCCAGCTAATTTTTGTATTT T C MFAP1 Ensembl:ENSG00000140259 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1434057391 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3164,RMVar_hsa_circ_267845,RMVar_hsa_circ_378570 8031 RMVar_ID_8031 Human_SNP_ID_575316077 A-to-I Human chr15 - 43813720 43813720 43813720 GGATCAGGAGGTCAGGAGTTCAAGACCAGCCTAGCCAAGATGGTGAAACCCCATCTCTACTAAAA GGATCAGGAGGTCAGGAGTTCAAGACCAGCCTGGCCAAGATGGTGAAACCCCATCTCTACTAAAA T C MFAP1 Ensembl:ENSG00000140259 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1438707526 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123979,RMVar_hsa_circ_3164,RMVar_hsa_circ_378570,RMVar_hsa_circ_171549 8032 RMVar_ID_8032 Human_SNP_ID_575317311 A-to-I Human chr15 - 43818647 43818646 43818647 TTTAAGCAATCCTCCTGCCTCAACCTTCCAAAATGCTGCGATTATAGGCATGAGCCACTGCACCT TTTAAGCAATCCTCCTGCCTCAACCTTCCAAA_TGCTGCGATTATAGGCATGAGCCACTGCACCT AT A MFAP1 Ensembl:ENSG00000140259 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1567177627 Functional Loss DEL dbSNP153 33..33 33 - - - 8033 RMVar_ID_8033 Human_SNP_ID_575317395 A-to-I Human chr15 - 43819009 43819009 43819009 TTTTGTATTTTTAGTAGAGACGGAGTTTTGCCATGTTGGGCAGGCTGGTCTCGAACTCCTAGCCT TTTTGTATTTTTAGTAGAGACGGAGTTTTGCCTTGTTGGGCAGGCTGGTCTCGAACTCCTAGCCT T A MFAP1 Ensembl:ENSG00000140259 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1230241693 Functional Loss SNV dbSNP153 33..33 33 - - - 8034 RMVar_ID_8034 Human_SNP_ID_575320515 A-to-I Human chr15 + 43829697 43829697 43829697 CCCGGCTAATTTTTTATATTTTCAGTAGAGACAGGGTTCCACCATGTTCGCCAGGATGGTCTCGA CCCGGCTAATTTTTTATATTTTCAGTAGAGACGGGGTTCCACCATGTTCGCCAGGATGGTCTCGA A G WDR76 Ensembl:ENSG00000092470 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223351072 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19272,RMVar_hsa_circ_368745 8035 RMVar_ID_8035 Human_SNP_ID_575320640 A-to-I Human chr15 + 43830127 43830127 43830127 GAGCTCAACCAGTCCTCCAACCTCAGACTCCCAAAGTGCTAGGATTATAGGCTTGAGCCACCACA GAGCTCAACCAGTCCTCCAACCTCAGACTCCCCAAGTGCTAGGATTATAGGCTTGAGCCACCACA A C WDR76 Ensembl:ENSG00000092470 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs527844112 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19272,RMVar_hsa_circ_368745 8036 RMVar_ID_8036 Human_SNP_ID_575321028 A-to-I Human chr15 + 43831475 43831475 43831475 TACTTTTTTTTTTTGAGACAGGGTCTCACTCTATTACCCAGGATGGAGTGCAGAGGCACGATCTC TACTTTTTTTTTTTGAGACAGGGTCTCACTCTGTTACCCAGGATGGAGTGCAGAGGCACGATCTC A G WDR76 Ensembl:ENSG00000092470 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs550415698 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19272,RMVar_hsa_circ_368745 8037 RMVar_ID_8037 Human_SNP_ID_575325455 A-to-I Human chr15 + 43846389 43846389 43846389 CTCACTGCAGCCTCAACTTCCCACGGTCAAGCAATTCTCCACCTCAGCTTCCTGCGTAGCTGGGA CTCACTGCAGCCTCAACTTCCCACGGTCAAGCGATTCTCCACCTCAGCTTCCTGCGTAGCTGGGA A G WDR76 Ensembl:ENSG00000092470 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1474448510 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 8038 RMVar_ID_8038 Human_SNP_ID_575325811 A-to-I Human chr15 + 43847560 43847560 43847560 TCTCTGCCTCAGCCTCCCAAGTGGCTGGGATTACAGGCGTCCGCTACCACACCTGGCTAATTTTT TCTCTGCCTCAGCCTCCCAAGTGGCTGGGATTGCAGGCGTCCGCTACCACACCTGGCTAATTTTT A G WDR76 Ensembl:ENSG00000092470 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1455370291 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 8039 RMVar_ID_8039 Human_SNP_ID_575325834 A-to-I Human chr15 + 43847606 43847606 43847606 CCACACCTGGCTAATTTTTTTGTTTTTTTAGTAGAGATGGGGTTTCACCATCTTGGCCAGGCTGG CCACACCTGGCTAATTTTTTTGTTTTTTTAGTGGAGATGGGGTTTCACCATCTTGGCCAGGCTGG A G WDR76 Ensembl:ENSG00000092470 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs550755484 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 8040 RMVar_ID_8040 Human_SNP_ID_575325941 A-to-I Human chr15 + 43848038 43848038 43848038 ATGGCTTAAGCCCACTAATTTGAGACCTGCCTAGGTGACATAGTGAGATGCCTGTCTCTTAAAAA ATGGCTTAAGCCCACTAATTTGAGACCTGCCTTGGTGACATAGTGAGATGCCTGTCTCTTAAAAA A T WDR76 Ensembl:ENSG00000092470 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1175617084 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 8041 RMVar_ID_8041 Human_SNP_ID_575326261 A-to-I Human chr15 + 43849054 43849054 43849054 AAAATTAGCCAAGCATGGTGGTGGGTGCCTGTAATCCCAGCGACTCAGGAGGCTGAGACAGGAGA AAAATTAGCCAAGCATGGTGGTGGGTGCCTGTGATCCCAGCGACTCAGGAGGCTGAGACAGGAGA A G WDR76 Ensembl:ENSG00000092470 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs537822000 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 8042 RMVar_ID_8042 Human_SNP_ID_575326440 A-to-I Human chr15 + 43849655 43849655 43849655 CTGCCTCCCCGGTTCAAGCAATTCTCTGCCTCAGCCTCCTGAGTAGCTGGAATTACAGGTGTCTG CTGCCTCCCCGGTTCAAGCAATTCTCTGCCTCGGCCTCCTGAGTAGCTGGAATTACAGGTGTCTG A G WDR76 Ensembl:ENSG00000092470 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs548203170 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 8043 RMVar_ID_8043 Human_SNP_ID_575326443 A-to-I Human chr15 + 43849677 43849677 43849677 TCTCTGCCTCAGCCTCCTGAGTAGCTGGAATTACAGGTGTCTGCCACCACGCCCGGCTAATTTTT TCTCTGCCTCAGCCTCCTGAGTAGCTGGAATTTCAGGTGTCTGCCACCACGCCCGGCTAATTTTT A T WDR76 Ensembl:ENSG00000092470 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1044229104 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 8044 RMVar_ID_8044 Human_SNP_ID_575329080 A-to-I Human chr15 + 43858480 43858480 43858480 CATGTTGAGGCTGGTTTCGAACTCCTGATCTCAGATGATCCACCTGCCTCCACCTCCCAAAGTGC CATGTTGAGGCTGGTTTCGAACTCCTGATCTCCGATGATCCACCTGCCTCCACCTCCCAAAGTGC A C WDR76 Ensembl:ENSG00000092470 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1260431156 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85971,RMVar_hsa_circ_171555,RMVar_hsa_circ_43869,RMVar_hsa_circ_373274,RMVar_hsa_circ_171557,RMVar_hsa_circ_101226,RMVar_hsa_circ_171558,RMVar_hsa_circ_323387,RMVar_hsa_circ_171559 8045 RMVar_ID_8045 Human_SNP_ID_575333731 A-to-I Human chr15 + 43875300 43875300 43875300 TTGAGCCTGGGAGGTCAAAGCTGCAGTAAACCAAGATCACACCACTGCATTCCAACCTGAGCAAC TTGAGCCTGGGAGGTCAAAGCTGCAGTAAACCGAGATCACACCACTGCATTCCAACCTGAGCAAC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355534375 Functional Loss SNV dbSNP153 33..33 33 - - - 8046 RMVar_ID_8046 Human_SNP_ID_575333918 A-to-I Human chr15 + 43875509 43875509 43875509 CCTAGTTTGTGTGTGTTTTGAGATGGAGTCTTACTCTGTCGCCCAGGTTGGAATGCAGTGGTGCA CCTAGTTTGTGTGTGTTTTGAGATGGAGTCTTGCTCTGTCGCCCAGGTTGGAATGCAGTGGTGCA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1288561110 Functional Loss SNV dbSNP153 33..33 33 - - - 8047 RMVar_ID_8047 Human_SNP_ID_575334127 A-to-I Human chr15 - 43876035 43876035 43876035 TCTGGGATGAGATTCAATGAAGTGGCCACACAATATAGTGAAGATAAAGCCAGGCAAGGGGGCGT TCTGGGATGAGATTCAATGAAGTGGCCACACAGTATAGTGAAGATAAAGCCAGGCAAGGGGGCGT T C FRMD5,PIN4P1 Ensembl:ENSG00000171877,Ensembl:ENSG00000227973 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878996051 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1829088 RMVar_hsa_circ_80728,RMVar_hsa_circ_17566,RMVar_hsa_circ_171562 8048 RMVar_ID_8048 Human_SNP_ID_575376810 A-to-I Human chr15 - 44050825 44050825 44050825 GGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCTGAGTGTGGTGGTGCGCACCTGTAATC GGTGAAACCCCGTCTCTACTAAAAATACAAAAGTTAGCTGAGTGTGGTGGTGCGCACCTGTAATC T C FRMD5 Ensembl:ENSG00000171877 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs948346389 Functional Loss SNV dbSNP153 33..33 33 - - - 8049 RMVar_ID_8049 Human_SNP_ID_575376817 A-to-I Human chr15 - 44050851 44050850 44050851 GAGTTTGAGACCAGCCTGGCCGGCATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCT GAGTTTGAGACCAGCCTGGCCGGCATGGTGAA_CCCCGTCTCTACTAAAAATACAAAAATTAGCT GT G FRMD5 Ensembl:ENSG00000171877 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1411275349 Functional Loss DEL dbSNP153 33..33 33 - - - 8050 RMVar_ID_8050 Human_SNP_ID_575376819 A-to-I Human chr15 - 44050853 44050853 44050853 AGGAGTTTGAGACCAGCCTGGCCGGCATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAG AGGAGTTTGAGACCAGCCTGGCCGGCATGGTGCAACCCCGTCTCTACTAAAAATACAAAAATTAG T G FRMD5 Ensembl:ENSG00000171877 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1436601998 Functional Loss SNV dbSNP153 33..33 33 - - - 8051 RMVar_ID_8051 Human_SNP_ID_575387062 A-to-I Human chr15 - 44095959 44095959 44095959 CAAGTGATCCACCCACCTCAGCCTCCCAAAGTATTGGGATTATAGGCGTGAGCCGCCGCACCCGG CAAGTGATCCACCCACCTCAGCCTCCCAAAGTTTTGGGATTATAGGCGTGAGCCGCCGCACCCGG T A FRMD5 Ensembl:ENSG00000171877 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1478624692 Functional Loss SNV dbSNP153 33..33 33 - - - 8052 RMVar_ID_8052 Human_SNP_ID_575391881 A-to-I Human chr15 - 44116328 44116328 44116328 TTGAGCCCAGGATTTCAGAGTTAAAGTGAGCTATGATTGTATCACTGCCCTCCAGCCTGGGCAAA TTGAGCCCAGGATTTCAGAGTTAAAGTGAGCTGTGATTGTATCACTGCCCTCCAGCCTGGGCAAA T C FRMD5 Ensembl:ENSG00000171877 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs547567977 Functional Loss SNV dbSNP153 33..33 33 - - - 8053 RMVar_ID_8053 Human_SNP_ID_575401077 A-to-I Human chr15 - 44154213 44154213 44154213 GCTCAATTGATCCTCCCACCTCAGCCTCCTGAATAGCTGAGATGAAAAGCATGCACCACCAAACC GCTCAATTGATCCTCCCACCTCAGCCTCCTGAGTAGCTGAGATGAAAAGCATGCACCACCAAACC T C FRMD5 Ensembl:ENSG00000171877 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1208207403 Functional Loss SNV dbSNP153 33..33 33 - - - 8054 RMVar_ID_8054 Human_SNP_ID_575405287 A-to-I Human chr15 - 44171842 44171837 44171843 CCAGAATCATTTGAACCCGGGAGACAGAAGTTACAGTGAGCCTAGATCACGCCGCTGTGCTCCAG CCAGAATCATTTGAACCCGGGAGACAGAAGT______GAGCCTAGATCACGCCGCTGTGCTCCAG CACTGTA C FRMD5 Ensembl:ENSG00000171877 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1469598759 Functional Loss DEL dbSNP153 32..37 33 - - - 8055 RMVar_ID_8055 Human_SNP_ID_575444501 A-to-I Human chr15 + 44329781 44329781 44329781 AAAATTAGCTGGGCATGATGGCGTATGCCTGTAGTCCTAGCTGCTTGGGAGGCTGAGGTGGGAGG AAAATTAGCTGGGCATGATGGCGTATGCCTGTGGTCCTAGCTGCTTGGGAGGCTGAGGTGGGAGG A G CASC4 Ensembl:ENSG00000166734 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1407859896 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16529,RMVar_hsa_circ_171572,RMVar_hsa_circ_297779,RMVar_hsa_circ_305032,RMVar_hsa_circ_320503,RMVar_hsa_circ_171573,RMVar_hsa_circ_291128,RMVar_hsa_circ_171571,RMVar_hsa_circ_294358,RMVar_hsa_circ_284629,RMVar_hsa_circ_171574,RMVar_hsa_circ_171575,RMVar_hsa_circ_171576 8056 RMVar_ID_8056 Human_SNP_ID_575446810 A-to-I Human chr15 + 44339522 44339522 44339522 CACCAAGCTCAGCTAATTTTTGTATTTTCAGTAGAGACGAGGTTTCACCATGTTGGCCAGCTGGT CACCAAGCTCAGCTAATTTTTGTATTTTCAGTGGAGACGAGGTTTCACCATGTTGGCCAGCTGGT A G CASC4 Ensembl:ENSG00000166734 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1279328489 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_297779,RMVar_hsa_circ_171571,RMVar_hsa_circ_284629,RMVar_hsa_circ_171578,RMVar_hsa_circ_171576,RMVar_hsa_circ_287679,RMVar_hsa_circ_324965,RMVar_hsa_circ_171581 8057 RMVar_ID_8057 Human_SNP_ID_575448664 A-to-I Human chr15 + 44346987 44346987 44346987 ATATCTTAGGAAAAAAAAAAATGGCTAGGCATAGTGGCACACACCTGTAGTCCTAGCTACTTGGG ATATCTTAGGAAAAAAAAAAATGGCTAGGCATGGTGGCACACACCTGTAGTCCTAGCTACTTGGG A G CASC4 Ensembl:ENSG00000166734 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1473228717 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_297779,RMVar_hsa_circ_171571,RMVar_hsa_circ_284629,RMVar_hsa_circ_171578,RMVar_hsa_circ_171576,RMVar_hsa_circ_287679,RMVar_hsa_circ_324965,RMVar_hsa_circ_171581 8058 RMVar_ID_8058 Human_SNP_ID_575457937 A-to-I Human chr15 + 44383806 44383806 44383806 TCAAATGATCCTCCCTTCTCACCTTCCTCAGTAGCTGAGACCACAGGCATGTGCCATCACACCTG TCAAATGATCCTCCCTTCTCACCTTCCTCAGTTGCTGAGACCACAGGCATGTGCCATCACACCTG A T CASC4 Ensembl:ENSG00000166734 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1279901515 Functional Loss SNV dbSNP153 33..33 33 - - - 8059 RMVar_ID_8059 Human_SNP_ID_575461428 A-to-I Human chr15 + 44398942 44398942 44398942 CACCCACCTCGGCCTCCCAAAATTCTGGGATTACAGGCGTGAGCCACCATGCCTGGCCCCGTAAT CACCCACCTCGGCCTCCCAAAATTCTGGGATTGCAGGCGTGAGCCACCATGCCTGGCCCCGTAAT A G CASC4 Ensembl:ENSG00000166734 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1023787754 Functional Loss SNV dbSNP153 33..33 33 - - - 8060 RMVar_ID_8060 Human_SNP_ID_575463326 A-to-I Human chr15 + 44407536 44407536 44407536 GGACTCAAGCAATCAGGCCACCTCGGTCTCCCAAAGTGTTCGGATTATAGGCATGAGCCGCTGCA GGACTCAAGCAATCAGGCCACCTCGGTCTCCCCAAGTGTTCGGATTATAGGCATGAGCCGCTGCA A C CASC4 Ensembl:ENSG00000166734 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs965535218 Functional Loss SNV dbSNP153 33..33 33 - - - 8061 RMVar_ID_8061 Human_SNP_ID_575474622 A-to-I Human chr15 + 44449734 44449734 44449734 AAAAGTAGCCAGGCGTGGTGGCACTAGCCTGTAATCCCAGCACTTTGGGAGGCTGAGAAGGATGA AAAAGTAGCCAGGCGTGGTGGCACTAGCCTGTTATCCCAGCACTTTGGGAGGCTGAGAAGGATGA A T CTDSPL2 Ensembl:ENSG00000137770 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs936968175 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_171584,RMVar_hsa_circ_92000 8062 RMVar_ID_8062 Human_SNP_ID_575477476 A-to-I Human chr15 + 44460135 44460135 44460135 TTTATTTTATTTTATTTATTTATTTTTGAAACAGAGTCTTGCTCTGTCTCCAGGCTGGAGTGCAG TTTATTTTATTTTATTTATTTATTTTTGAAACGGAGTCTTGCTCTGTCTCCAGGCTGGAGTGCAG A G CTDSPL2 Ensembl:ENSG00000137770 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1421260204 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12516381 RMVar_hsa_circ_69757,RMVar_hsa_circ_171584,RMVar_hsa_circ_92000,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 8063 RMVar_ID_8063 Human_SNP_ID_575480298 A-to-I Human chr15 + 44470589 44470588 44470589 CCTACCTCAGCCTCCCGAGTAAGTGGGATTACAGGCACCTGCCACCACTCCCAGCTAATTTTTAT CCTACCTCAGCCTCCCGAGTAAGTGGGATTAC_GGCACCTGCCACCACTCCCAGCTAATTTTTAT CA C CTDSPL2 Ensembl:ENSG00000137770 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1407104492 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_69757,RMVar_hsa_circ_171584,RMVar_hsa_circ_92000,RMVar_hsa_circ_354023,RMVar_hsa_circ_327814,RMVar_hsa_circ_278698,RMVar_hsa_circ_35505,RMVar_hsa_circ_65780,RMVar_hsa_circ_171589,RMVar_hsa_circ_12303,RMVar_hsa_circ_171588 8064 RMVar_ID_8064 Human_SNP_ID_575481288 A-to-I Human chr15 + 44474242 44474242 44474242 CACGCCTGTAACGCCTGTAATCCTAGCACTTTAGGAGGCCGAGAAGGGCAGAGGGTGGATTGCCT CACGCCTGTAACGCCTGTAATCCTAGCACTTTCGGAGGCCGAGAAGGGCAGAGGGTGGATTGCCT A C CTDSPL2 Ensembl:ENSG00000137770 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1465801496 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69757,RMVar_hsa_circ_171584,RMVar_hsa_circ_92000,RMVar_hsa_circ_354023,RMVar_hsa_circ_327814,RMVar_hsa_circ_278698,RMVar_hsa_circ_35505,RMVar_hsa_circ_65780,RMVar_hsa_circ_171589,RMVar_hsa_circ_12303,RMVar_hsa_circ_171588 8065 RMVar_ID_8065 Human_SNP_ID_575487264 A-to-I Human chr15 + 44497726 44497726 44497726 TAAAAATTTGTATTTTAGGGACTGGGTGTGGTAGCTCATGCCTGTAATCCTAGAACTTTGGGAGG TAAAAATTTGTATTTTAGGGACTGGGTGTGGTGGCTCATGCCTGTAATCCTAGAACTTTGGGAGG A G CTDSPL2 Ensembl:ENSG00000137770 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1490803799 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1278,RMVar_hsa_circ_354023,RMVar_hsa_circ_35505,RMVar_hsa_circ_65780,RMVar_hsa_circ_171589,RMVar_hsa_circ_68277,RMVar_hsa_circ_286875,RMVar_hsa_circ_171591,RMVar_hsa_circ_361990,RMVar_hsa_circ_27347,RMVar_hsa_circ_52061,RMVar_hsa_circ_97612,RMVar_hsa_circ_336422,RMVar_hsa_circ_53651,RMVar_hsa_circ_171598,RMVar_hsa_circ_171597,RMVar_hsa_circ_371086,RMVar_hsa_circ_69114,RMVar_hsa_circ_16500,RMVar_hsa_circ_171601,RMVar_hsa_circ_306118,RMVar_hsa_circ_327231,RMVar_hsa_circ_310054,RMVar_hsa_circ_171602,RMVar_hsa_circ_171603 8066 RMVar_ID_8066 Human_SNP_ID_575488652 A-to-I Human chr15 + 44504123 44504123 44504123 TAATCCCAGCACTTTGGGAGGCGGAGATGGGCAGATCACCTGAGGCCAGGAGTTCAGGACCACCC TAATCCCAGCACTTTGGGAGGCGGAGATGGGCCGATCACCTGAGGCCAGGAGTTCAGGACCACCC A C CTDSPL2 Ensembl:ENSG00000137770 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1209351798 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1278,RMVar_hsa_circ_35505,RMVar_hsa_circ_65780,RMVar_hsa_circ_68277,RMVar_hsa_circ_361990,RMVar_hsa_circ_27347,RMVar_hsa_circ_52061,RMVar_hsa_circ_97612,RMVar_hsa_circ_53651,RMVar_hsa_circ_171598,RMVar_hsa_circ_16500,RMVar_hsa_circ_306118,RMVar_hsa_circ_327231,RMVar_hsa_circ_310054,RMVar_hsa_circ_171602,RMVar_hsa_circ_171605,RMVar_hsa_circ_115675 8067 RMVar_ID_8067 Human_SNP_ID_575488804 A-to-I Human chr15 + 44504749 44504749 44504749 AAAATTAGCCGGGCATGGTGGGGAGCACCTATAGTCCCAGCTACTCGATAGGCTGAGGCAGGAGG AAAATTAGCCGGGCATGGTGGGGAGCACCTATGGTCCCAGCTACTCGATAGGCTGAGGCAGGAGG A G CTDSPL2 Ensembl:ENSG00000137770 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1406714333 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12516874 RMVar_hsa_circ_1278,RMVar_hsa_circ_35505,RMVar_hsa_circ_65780,RMVar_hsa_circ_68277,RMVar_hsa_circ_361990,RMVar_hsa_circ_27347,RMVar_hsa_circ_52061,RMVar_hsa_circ_97612,RMVar_hsa_circ_53651,RMVar_hsa_circ_171598,RMVar_hsa_circ_16500,RMVar_hsa_circ_306118,RMVar_hsa_circ_327231,RMVar_hsa_circ_310054,RMVar_hsa_circ_171602,RMVar_hsa_circ_171605,RMVar_hsa_circ_115675 8068 RMVar_ID_8068 Human_SNP_ID_575488998 A-to-I Human chr15 + 44505544 44505544 44505544 TCACCTGAGGTCAGAGAGTTCGAGACCAGCCTAAACAACATGGTGAAACCCTGTCTCTACTAAAA TCACCTGAGGTCAGAGAGTTCGAGACCAGCCTCAACAACATGGTGAAACCCTGTCTCTACTAAAA A C CTDSPL2 Ensembl:ENSG00000137770 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs188209801 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1278,RMVar_hsa_circ_35505,RMVar_hsa_circ_65780,RMVar_hsa_circ_68277,RMVar_hsa_circ_361990,RMVar_hsa_circ_27347,RMVar_hsa_circ_52061,RMVar_hsa_circ_97612,RMVar_hsa_circ_53651,RMVar_hsa_circ_171598,RMVar_hsa_circ_16500,RMVar_hsa_circ_306118,RMVar_hsa_circ_327231,RMVar_hsa_circ_310054,RMVar_hsa_circ_171602,RMVar_hsa_circ_171605,RMVar_hsa_circ_115675 8069 RMVar_ID_8069 Human_SNP_ID_575488999 A-to-I Human chr15 + 44505544 44505544 44505544 TCACCTGAGGTCAGAGAGTTCGAGACCAGCCTAAACAACATGGTGAAACCCTGTCTCTACTAAAA TCACCTGAGGTCAGAGAGTTCGAGACCAGCCTGAACAACATGGTGAAACCCTGTCTCTACTAAAA A G CTDSPL2 Ensembl:ENSG00000137770 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs188209801 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1278,RMVar_hsa_circ_35505,RMVar_hsa_circ_65780,RMVar_hsa_circ_68277,RMVar_hsa_circ_361990,RMVar_hsa_circ_27347,RMVar_hsa_circ_52061,RMVar_hsa_circ_97612,RMVar_hsa_circ_53651,RMVar_hsa_circ_171598,RMVar_hsa_circ_16500,RMVar_hsa_circ_306118,RMVar_hsa_circ_327231,RMVar_hsa_circ_310054,RMVar_hsa_circ_171602,RMVar_hsa_circ_171605,RMVar_hsa_circ_115675 8070 RMVar_ID_8070 Human_SNP_ID_575489203 A-to-I Human chr15 + 44506210 44506210 44506210 TGCTACTGAGGCCGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTTACCCTGTTGGCCAGGC TGCTACTGAGGCCGGCTAATTTTTGTATTTTTGGTAGAGATGGGGTTTTACCCTGTTGGCCAGGC A G CTDSPL2 Ensembl:ENSG00000137770 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs945630284 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1278,RMVar_hsa_circ_35505,RMVar_hsa_circ_65780,RMVar_hsa_circ_68277,RMVar_hsa_circ_361990,RMVar_hsa_circ_27347,RMVar_hsa_circ_52061,RMVar_hsa_circ_97612,RMVar_hsa_circ_53651,RMVar_hsa_circ_171598,RMVar_hsa_circ_16500,RMVar_hsa_circ_306118,RMVar_hsa_circ_327231,RMVar_hsa_circ_310054,RMVar_hsa_circ_171602,RMVar_hsa_circ_171605,RMVar_hsa_circ_115675 8071 RMVar_ID_8071 Human_SNP_ID_575489217 A-to-I Human chr15 + 44506239 44506239 44506239 TTTAGTAGAGATGGGGTTTTACCCTGTTGGCCAGGCTGGTCTTGAACTCCTCACCTCAAGTGATC TTTAGTAGAGATGGGGTTTTACCCTGTTGGCCGGGCTGGTCTTGAACTCCTCACCTCAAGTGATC A G CTDSPL2 Ensembl:ENSG00000137770 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs760698170 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1278,RMVar_hsa_circ_35505,RMVar_hsa_circ_65780,RMVar_hsa_circ_68277,RMVar_hsa_circ_361990,RMVar_hsa_circ_27347,RMVar_hsa_circ_52061,RMVar_hsa_circ_97612,RMVar_hsa_circ_53651,RMVar_hsa_circ_171598,RMVar_hsa_circ_16500,RMVar_hsa_circ_306118,RMVar_hsa_circ_327231,RMVar_hsa_circ_310054,RMVar_hsa_circ_171602,RMVar_hsa_circ_171605,RMVar_hsa_circ_115675 8072 RMVar_ID_8072 Human_SNP_ID_575489458 A-to-I Human chr15 + 44506989 44506989 44506989 CAGGGTTTCACCGTGTAAGCCAGGACGGTCTCAATCTCCTGACCTCGTGATCCGCCCACCTCGGC CAGGGTTTCACCGTGTAAGCCAGGACGGTCTCCATCTCCTGACCTCGTGATCCGCCCACCTCGGC A C CTDSPL2 Ensembl:ENSG00000137770 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1398099458 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1278,RMVar_hsa_circ_35505,RMVar_hsa_circ_65780,RMVar_hsa_circ_68277,RMVar_hsa_circ_361990,RMVar_hsa_circ_27347,RMVar_hsa_circ_52061,RMVar_hsa_circ_97612,RMVar_hsa_circ_53651,RMVar_hsa_circ_171598,RMVar_hsa_circ_16500,RMVar_hsa_circ_306118,RMVar_hsa_circ_327231,RMVar_hsa_circ_310054,RMVar_hsa_circ_171602,RMVar_hsa_circ_171605,RMVar_hsa_circ_115675 8073 RMVar_ID_8073 Human_SNP_ID_575489459 A-to-I Human chr15 + 44506989 44506989 44506989 CAGGGTTTCACCGTGTAAGCCAGGACGGTCTCAATCTCCTGACCTCGTGATCCGCCCACCTCGGC CAGGGTTTCACCGTGTAAGCCAGGACGGTCTCGATCTCCTGACCTCGTGATCCGCCCACCTCGGC A G CTDSPL2 Ensembl:ENSG00000137770 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1398099458 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1278,RMVar_hsa_circ_35505,RMVar_hsa_circ_65780,RMVar_hsa_circ_68277,RMVar_hsa_circ_361990,RMVar_hsa_circ_27347,RMVar_hsa_circ_52061,RMVar_hsa_circ_97612,RMVar_hsa_circ_53651,RMVar_hsa_circ_171598,RMVar_hsa_circ_16500,RMVar_hsa_circ_306118,RMVar_hsa_circ_327231,RMVar_hsa_circ_310054,RMVar_hsa_circ_171602,RMVar_hsa_circ_171605,RMVar_hsa_circ_115675 8074 RMVar_ID_8074 Human_SNP_ID_575489475 A-to-I Human chr15 + 44507041 44507040 44507041 CGCCCACCTCGGCCTCCCAAAGTGCTGAGATTACAGGCGTGAGCCACCGCGCCTGGCTTTTTTTG CGCCCACCTCGGCCTCCCAAAGTGCTGAGATT_CAGGCGTGAGCCACCGCGCCTGGCTTTTTTTG TA T CTDSPL2 Ensembl:ENSG00000137770 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1175681275 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_1278,RMVar_hsa_circ_35505,RMVar_hsa_circ_65780,RMVar_hsa_circ_68277,RMVar_hsa_circ_361990,RMVar_hsa_circ_27347,RMVar_hsa_circ_52061,RMVar_hsa_circ_97612,RMVar_hsa_circ_53651,RMVar_hsa_circ_171598,RMVar_hsa_circ_16500,RMVar_hsa_circ_306118,RMVar_hsa_circ_327231,RMVar_hsa_circ_310054,RMVar_hsa_circ_171602,RMVar_hsa_circ_171605,RMVar_hsa_circ_115675 8075 RMVar_ID_8075 Human_SNP_ID_575489476 A-to-I Human chr15 + 44507041 44507041 44507041 CGCCCACCTCGGCCTCCCAAAGTGCTGAGATTACAGGCGTGAGCCACCGCGCCTGGCTTTTTTTG CGCCCACCTCGGCCTCCCAAAGTGCTGAGATTGCAGGCGTGAGCCACCGCGCCTGGCTTTTTTTG A G CTDSPL2 Ensembl:ENSG00000137770 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1373680285 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1278,RMVar_hsa_circ_35505,RMVar_hsa_circ_65780,RMVar_hsa_circ_68277,RMVar_hsa_circ_361990,RMVar_hsa_circ_27347,RMVar_hsa_circ_52061,RMVar_hsa_circ_97612,RMVar_hsa_circ_53651,RMVar_hsa_circ_171598,RMVar_hsa_circ_16500,RMVar_hsa_circ_306118,RMVar_hsa_circ_327231,RMVar_hsa_circ_310054,RMVar_hsa_circ_171602,RMVar_hsa_circ_171605,RMVar_hsa_circ_115675 8076 RMVar_ID_8076 Human_SNP_ID_575489512 A-to-I Human chr15 + 44507133 44507133 44507133 AGACTGAGTCTCGCTACTCTGTCGCCCAGGCTAGAGTATGGTGGCACCATCTCAGCTCACTGCAA AGACTGAGTCTCGCTACTCTGTCGCCCAGGCTGGAGTATGGTGGCACCATCTCAGCTCACTGCAA A G CTDSPL2 Ensembl:ENSG00000137770 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1237954798 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1278,RMVar_hsa_circ_35505,RMVar_hsa_circ_65780,RMVar_hsa_circ_68277,RMVar_hsa_circ_361990,RMVar_hsa_circ_27347,RMVar_hsa_circ_52061,RMVar_hsa_circ_97612,RMVar_hsa_circ_53651,RMVar_hsa_circ_171598,RMVar_hsa_circ_16500,RMVar_hsa_circ_306118,RMVar_hsa_circ_327231,RMVar_hsa_circ_310054,RMVar_hsa_circ_171602,RMVar_hsa_circ_171605,RMVar_hsa_circ_115675 8077 RMVar_ID_8077 Human_SNP_ID_575489749 A-to-I Human chr15 + 44508136 44508136 44508136 ACAGGGTTTCATTCTGCCACCCAGGCTAGAGTACAGTGACATGATCACATCTCACTGCAGCCTCA ACAGGGTTTCATTCTGCCACCCAGGCTAGAGTGCAGTGACATGATCACATCTCACTGCAGCCTCA A G CTDSPL2 Ensembl:ENSG00000137770 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs576555319 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12516943 RMVar_hsa_circ_1278,RMVar_hsa_circ_35505,RMVar_hsa_circ_65780,RMVar_hsa_circ_68277,RMVar_hsa_circ_361990,RMVar_hsa_circ_27347,RMVar_hsa_circ_52061,RMVar_hsa_circ_97612,RMVar_hsa_circ_53651,RMVar_hsa_circ_171598,RMVar_hsa_circ_16500,RMVar_hsa_circ_306118,RMVar_hsa_circ_327231,RMVar_hsa_circ_310054,RMVar_hsa_circ_171602,RMVar_hsa_circ_171605,RMVar_hsa_circ_115675 8078 RMVar_ID_8078 Human_SNP_ID_575489750 A-to-I Human chr15 + 44508136 44508136 44508136 ACAGGGTTTCATTCTGCCACCCAGGCTAGAGTACAGTGACATGATCACATCTCACTGCAGCCTCA ACAGGGTTTCATTCTGCCACCCAGGCTAGAGTTCAGTGACATGATCACATCTCACTGCAGCCTCA A T CTDSPL2 Ensembl:ENSG00000137770 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs576555319 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12516943 RMVar_hsa_circ_1278,RMVar_hsa_circ_35505,RMVar_hsa_circ_65780,RMVar_hsa_circ_68277,RMVar_hsa_circ_361990,RMVar_hsa_circ_27347,RMVar_hsa_circ_52061,RMVar_hsa_circ_97612,RMVar_hsa_circ_53651,RMVar_hsa_circ_171598,RMVar_hsa_circ_16500,RMVar_hsa_circ_306118,RMVar_hsa_circ_327231,RMVar_hsa_circ_310054,RMVar_hsa_circ_171602,RMVar_hsa_circ_171605,RMVar_hsa_circ_115675 8079 RMVar_ID_8079 Human_SNP_ID_575489782 A-to-I Human chr15 + 44508273 44508272 44508274 CCTGGCTAATTTTTGTATTTTTTTGTAGAGACAGGGTTTCGCCATGTTGCCCAGGCTAGTCTCAA CCTGGCTAATTTTTGTATTTTTTTGTAGAGAC__GGTTTCGCCATGTTGCCCAGGCTAGTCTCAA CAG C CTDSPL2 Ensembl:ENSG00000137770 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs368669977 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_1278,RMVar_hsa_circ_35505,RMVar_hsa_circ_65780,RMVar_hsa_circ_68277,RMVar_hsa_circ_361990,RMVar_hsa_circ_27347,RMVar_hsa_circ_52061,RMVar_hsa_circ_97612,RMVar_hsa_circ_53651,RMVar_hsa_circ_171598,RMVar_hsa_circ_16500,RMVar_hsa_circ_306118,RMVar_hsa_circ_327231,RMVar_hsa_circ_310054,RMVar_hsa_circ_171602,RMVar_hsa_circ_171605,RMVar_hsa_circ_115675 8080 RMVar_ID_8080 Human_SNP_ID_575489858 A-to-I Human chr15 + 44508635 44508635 44508635 AAAAGTTTCAAAGATGTTTCTTTTTGAAAGTTATGGTCTGCCGGGCGCTGTGGCTAGCCCCTGTA AAAAGTTTCAAAGATGTTTCTTTTTGAAAGTTCTGGTCTGCCGGGCGCTGTGGCTAGCCCCTGTA A C CTDSPL2 Ensembl:ENSG00000137770 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1314247625 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6428965,Human_RBP_ID_12516957 RMVar_hsa_circ_1278,RMVar_hsa_circ_35505,RMVar_hsa_circ_65780,RMVar_hsa_circ_68277,RMVar_hsa_circ_361990,RMVar_hsa_circ_27347,RMVar_hsa_circ_52061,RMVar_hsa_circ_97612,RMVar_hsa_circ_53651,RMVar_hsa_circ_171598,RMVar_hsa_circ_16500,RMVar_hsa_circ_306118,RMVar_hsa_circ_327231,RMVar_hsa_circ_310054,RMVar_hsa_circ_171602,RMVar_hsa_circ_171605,RMVar_hsa_circ_115675 8081 RMVar_ID_8081 Human_SNP_ID_575489904 A-to-I Human chr15 + 44508780 44508780 44508780 CTGTGTCTACTAAAAATACAAAAAACTTAGGCATGGTGGCGGAGCCCTGTCAGCTGAGCTATTCG CTGTGTCTACTAAAAATACAAAAAACTTAGGCTTGGTGGCGGAGCCCTGTCAGCTGAGCTATTCG A T CTDSPL2 Ensembl:ENSG00000137770 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs762776674 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6428967 RMVar_hsa_circ_1278,RMVar_hsa_circ_35505,RMVar_hsa_circ_65780,RMVar_hsa_circ_68277,RMVar_hsa_circ_361990,RMVar_hsa_circ_27347,RMVar_hsa_circ_52061,RMVar_hsa_circ_97612,RMVar_hsa_circ_53651,RMVar_hsa_circ_171598,RMVar_hsa_circ_16500,RMVar_hsa_circ_306118,RMVar_hsa_circ_327231,RMVar_hsa_circ_310054,RMVar_hsa_circ_171602,RMVar_hsa_circ_171605,RMVar_hsa_circ_115675 8082 RMVar_ID_8082 Human_SNP_ID_575490130 A-to-I Human chr15 + 44509689 44509689 44509689 ATATATATGGCTGGGTGCGGTGGCTCATGCCTATAATCCCAGGACTTTGGGAGGCCAAGGCAGGC ATATATATGGCTGGGTGCGGTGGCTCATGCCTGTAATCCCAGGACTTTGGGAGGCCAAGGCAGGC A G CTDSPL2 Ensembl:ENSG00000137770 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1325716019 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1278,RMVar_hsa_circ_35505,RMVar_hsa_circ_65780,RMVar_hsa_circ_68277,RMVar_hsa_circ_361990,RMVar_hsa_circ_27347,RMVar_hsa_circ_52061,RMVar_hsa_circ_97612,RMVar_hsa_circ_53651,RMVar_hsa_circ_171598,RMVar_hsa_circ_16500,RMVar_hsa_circ_306118,RMVar_hsa_circ_327231,RMVar_hsa_circ_310054,RMVar_hsa_circ_171602,RMVar_hsa_circ_171605,RMVar_hsa_circ_115675 8083 RMVar_ID_8083 Human_SNP_ID_575490224 A-to-I Human chr15 + 44510018 44510007 44510019 ACAACACCTTTTTTTTTTTGAGACGGAGTCTCACTCTGTTGCCCAGACTGGAGTGCAGTAGCGCA ACAACACCTTTTTTTTTTTGAG____________TCTGTTGCCCAGACTGGAGTGCAGTAGCGCA GACGGAGTCTCAC G CTDSPL2 Ensembl:ENSG00000137770 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs997861208 Functional Loss DEL dbSNP153 23..34 33 - - - RMVar_hsa_circ_1278,RMVar_hsa_circ_35505,RMVar_hsa_circ_65780,RMVar_hsa_circ_68277,RMVar_hsa_circ_361990,RMVar_hsa_circ_27347,RMVar_hsa_circ_52061,RMVar_hsa_circ_97612,RMVar_hsa_circ_53651,RMVar_hsa_circ_171598,RMVar_hsa_circ_16500,RMVar_hsa_circ_306118,RMVar_hsa_circ_327231,RMVar_hsa_circ_310054,RMVar_hsa_circ_171602,RMVar_hsa_circ_171605,RMVar_hsa_circ_115675 8084 RMVar_ID_8084 Human_SNP_ID_575490258 A-to-I Human chr15 + 44510127 44510127 44510127 CCGGTCTCAGCCTCCCCAGTAGCTGGGACTACAGGTGCATGCCACCACGTCCAGCTAATTTTTGT CCGGTCTCAGCCTCCCCAGTAGCTGGGACTACGGGTGCATGCCACCACGTCCAGCTAATTTTTGT A G CTDSPL2 Ensembl:ENSG00000137770 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs905716594 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1278,RMVar_hsa_circ_35505,RMVar_hsa_circ_65780,RMVar_hsa_circ_68277,RMVar_hsa_circ_361990,RMVar_hsa_circ_27347,RMVar_hsa_circ_52061,RMVar_hsa_circ_97612,RMVar_hsa_circ_53651,RMVar_hsa_circ_171598,RMVar_hsa_circ_16500,RMVar_hsa_circ_306118,RMVar_hsa_circ_327231,RMVar_hsa_circ_310054,RMVar_hsa_circ_171602,RMVar_hsa_circ_171605,RMVar_hsa_circ_115675 8085 RMVar_ID_8085 Human_SNP_ID_575490270 A-to-I Human chr15 + 44510178 44510178 44510178 CAGCTAATTTTTGTATATTTAGTAGTATATTTAGTAGAGACAGGGTTTCAACATGTTAGTCTGGC CAGCTAATTTTTGTATATTTAGTAGTATATTTCGTAGAGACAGGGTTTCAACATGTTAGTCTGGC A C CTDSPL2 Ensembl:ENSG00000137770 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs938063690 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1278,RMVar_hsa_circ_35505,RMVar_hsa_circ_65780,RMVar_hsa_circ_68277,RMVar_hsa_circ_361990,RMVar_hsa_circ_27347,RMVar_hsa_circ_52061,RMVar_hsa_circ_97612,RMVar_hsa_circ_53651,RMVar_hsa_circ_171598,RMVar_hsa_circ_16500,RMVar_hsa_circ_306118,RMVar_hsa_circ_327231,RMVar_hsa_circ_310054,RMVar_hsa_circ_171602,RMVar_hsa_circ_171605,RMVar_hsa_circ_115675 8086 RMVar_ID_8086 Human_SNP_ID_575490272 A-to-I Human chr15 + 44510187 44510187 44510187 TTTGTATATTTAGTAGTATATTTAGTAGAGACAGGGTTTCAACATGTTAGTCTGGCTGGTCTCAA TTTGTATATTTAGTAGTATATTTAGTAGAGACGGGGTTTCAACATGTTAGTCTGGCTGGTCTCAA A G CTDSPL2 Ensembl:ENSG00000137770 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1056668615 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12516975,Human_RBP_ID_23161711 RMVar_hsa_circ_1278,RMVar_hsa_circ_35505,RMVar_hsa_circ_65780,RMVar_hsa_circ_68277,RMVar_hsa_circ_361990,RMVar_hsa_circ_27347,RMVar_hsa_circ_52061,RMVar_hsa_circ_97612,RMVar_hsa_circ_53651,RMVar_hsa_circ_171598,RMVar_hsa_circ_16500,RMVar_hsa_circ_306118,RMVar_hsa_circ_327231,RMVar_hsa_circ_310054,RMVar_hsa_circ_171602,RMVar_hsa_circ_171605,RMVar_hsa_circ_115675 8087 RMVar_ID_8087 Human_SNP_ID_575491574 A-to-I Human chr15 + 44515615 44515615 44515615 TAATAGGGCCAGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGTCTGGCTA TAATAGGGCCAGGCGCGGTGGCTCACGCCTGTTATCCCAGCACTTTGGGAGGCTGAGTCTGGCTA A T CTDSPL2 Ensembl:ENSG00000137770 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1304924819 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1278,RMVar_hsa_circ_35505,RMVar_hsa_circ_27347,RMVar_hsa_circ_52061,RMVar_hsa_circ_97612,RMVar_hsa_circ_171598,RMVar_hsa_circ_16500,RMVar_hsa_circ_306118,RMVar_hsa_circ_327231,RMVar_hsa_circ_171602,RMVar_hsa_circ_329597,RMVar_hsa_circ_348059,RMVar_hsa_circ_171606 8088 RMVar_ID_8088 Human_SNP_ID_575493451 A-to-I Human chr15 + 44522962 44522962 44522962 GTTTGGCCTCTATTGCTTGATGAAACTTTGGCAGGATGTAGTGGTGCACACCTATTTAATCCCAC GTTTGGCCTCTATTGCTTGATGAAACTTTGGCGGGATGTAGTGGTGCACACCTATTTAATCCCAC A G CTDSPL2 Ensembl:ENSG00000137770 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4611428 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_635 RMVar_hsa_circ_171608,RMVar_hsa_circ_109903 8089 RMVar_ID_8089 Human_SNP_ID_575493512 A-to-I Human chr15 + 44523180 44523180 44523180 CACCACGCCTGGCTAATTTTTGTATTTTTAGTAGAGACTGGGTTTCACCACATTGGCCAGGCTGA CACCACGCCTGGCTAATTTTTGTATTTTTAGTGGAGACTGGGTTTCACCACATTGGCCAGGCTGA A G CTDSPL2 Ensembl:ENSG00000137770 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1433214017 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_171608,RMVar_hsa_circ_109903 8090 RMVar_ID_8090 Human_SNP_ID_575497915 A-to-I Human chr15 + 44539469 44539469 44539469 TCGCTCTGTCACCCAGGCTGGAGTGCAGTGGCACAATCTCCGCTCACTGCAAGCTCCGCCTCCCA TCGCTCTGTCACCCAGGCTGGAGTGCAGTGGCGCAATCTCCGCTCACTGCAAGCTCCGCCTCCCA A G EIF3J Ensembl:ENSG00000104131 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1485020461 Functional Loss SNV dbSNP153 33..33 33 - - - 8091 RMVar_ID_8091 Human_SNP_ID_575497916 A-to-I Human chr15 + 44539471 44539471 44539471 GCTCTGTCACCCAGGCTGGAGTGCAGTGGCACAATCTCCGCTCACTGCAAGCTCCGCCTCCCAGG GCTCTGTCACCCAGGCTGGAGTGCAGTGGCACGATCTCCGCTCACTGCAAGCTCCGCCTCCCAGG A G EIF3J Ensembl:ENSG00000104131 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1186092571 Functional Loss SNV dbSNP153 33..33 33 - - - 8092 RMVar_ID_8092 Human_SNP_ID_575499347 A-to-I Human chr15 + 44544443 44544443 44544443 TAGTAGAAAACTGGCCAGGCGTGGTGGCTCACACCTGTAATCCCAACACTTTGGGAGGCTGAGGT TAGTAGAAAACTGGCCAGGCGTGGTGGCTCACGCCTGTAATCCCAACACTTTGGGAGGCTGAGGT A G EIF3J Ensembl:ENSG00000104131 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1385279934 Functional Loss SNV dbSNP153 33..33 33 - - - 8093 RMVar_ID_8093 Human_SNP_ID_575499382 A-to-I Human chr15 + 44544570 44544570 44544570 TACTAAAAATACAAAATTAGCCAGTTCGTGGTAGCACATGCCTGTAATCCCAGCCACTTGGGAGG TACTAAAAATACAAAATTAGCCAGTTCGTGGTGGCACATGCCTGTAATCCCAGCCACTTGGGAGG A G EIF3J Ensembl:ENSG00000104131 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1475622502 Functional Loss SNV dbSNP153 33..33 33 - - - 8094 RMVar_ID_8094 Human_SNP_ID_575500376 A-to-I Human chr15 + 44548276 44548276 44548276 GTCTCTACTAAAAATACAAAAATTAGCCCGGCATGATGGTGGACACCTGTAATCCCAGCTACTCC GTCTCTACTAAAAATACAAAAATTAGCCCGGCGTGATGGTGGACACCTGTAATCCCAGCTACTCC A G EIF3J Ensembl:ENSG00000104131 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1183993390 Functional Loss SNV dbSNP153 33..33 33 - - - 8095 RMVar_ID_8095 Human_SNP_ID_575501363 A-to-I Human chr15 + 44551893 44551893 44551893 TGCTCTGTCGCTAGGCTGGAGTACAGTGGCACAATCTCGGCTCAGTGCAACCTCTGCCTCCCGAA TGCTCTGTCGCTAGGCTGGAGTACAGTGGCACGATCTCGGCTCAGTGCAACCTCTGCCTCCCGAA A G EIF3J Ensembl:ENSG00000104131 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1003022891 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_30737,RMVar_hsa_circ_300962,RMVar_hsa_circ_332229,RMVar_hsa_circ_171609 8096 RMVar_ID_8096 Human_SNP_ID_575501684 A-to-I Human chr15 + 44553149 44553149 44553149 TTGAGGCTGCAGTGAGCCATGACTGCGCCACTACACTCCAGCCTAGGTGACAGAGCAAGATCCTG TTGAGGCTGCAGTGAGCCATGACTGCGCCACTGCACTCCAGCCTAGGTGACAGAGCAAGATCCTG A G EIF3J Ensembl:ENSG00000104131 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1273311035 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25141743 RMVar_hsa_circ_30737,RMVar_hsa_circ_300962,RMVar_hsa_circ_332229,RMVar_hsa_circ_171609 8097 RMVar_ID_8097 Human_SNP_ID_575504701 A-to-I Human chr15 + 44563538 44563538 44563538 TTTTCTAATTTTAGTAGAGACAGCGTTCTGCTATGTTGGCTAGGCTGGTGTTGAACTCCGGGCCT TTTTCTAATTTTAGTAGAGACAGCGTTCTGCTCTGTTGGCTAGGCTGGTGTTGAACTCCGGGCCT A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs557188718 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4323280,Human_RBP_ID_12518038,Human_RBP_ID_23652983 8098 RMVar_ID_8098 Human_SNP_ID_575504702 A-to-I Human chr15 + 44563538 44563538 44563538 TTTTCTAATTTTAGTAGAGACAGCGTTCTGCTATGTTGGCTAGGCTGGTGTTGAACTCCGGGCCT TTTTCTAATTTTAGTAGAGACAGCGTTCTGCTGTGTTGGCTAGGCTGGTGTTGAACTCCGGGCCT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs557188718 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4323280,Human_RBP_ID_12518038,Human_RBP_ID_23652983 8099 RMVar_ID_8099 Human_SNP_ID_575504883 A-to-I Human chr15 - 44564067 44564067 44564067 AATCACTTGAACCTGGGGACAGAGGCTGCAGTAAGCTGAGATCGTGCCACTATACTCCAGCCTGG AATCACTTGAACCTGGGGACAGAGGCTGCAGTGAGCTGAGATCGTGCCACTATACTCCAGCCTGG T C SPG11 Ensembl:ENSG00000104133 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs940846281 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_171615,RMVar_hsa_circ_171616 8100 RMVar_ID_8100 Human_SNP_ID_575505767 A-to-I Human chr15 + 44566730 44566730 44566730 ACCTCAACATTCTTTTTTTGAGATGGAGTCACACTCTGTCACCTACGCTGGAGTGCAATGGGCGC ACCTCAACATTCTTTTTTTGAGATGGAGTCACGCTCTGTCACCTACGCTGGAGTGCAATGGGCGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170046512 Functional Loss SNV dbSNP153 33..33 33 - - - 8101 RMVar_ID_8101 Human_SNP_ID_575505787 A-to-I Human chr15 + 44566779 44566779 44566779 GGAGTGCAATGGGCGCGATCTTGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGTGATCCACCT GGAGTGCAATGGGCGCGATCTTGGCTCACTGCGACCTCCGCCTCCCGGGTTCAAGTGATCCACCT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1408412425 Functional Loss SNV dbSNP153 33..33 33 - - - 8102 RMVar_ID_8102 Human_SNP_ID_575505821 A-to-I Human chr15 + 44566903 44566903 44566903 TTTTTGTATTTTAGTAGAGACAGGATTGCACCATGTTGCCCAGGCTGGTGTTGAACTCCTGAGCT TTTTTGTATTTTAGTAGAGACAGGATTGCACCGTGTTGCCCAGGCTGGTGTTGAACTCCTGAGCT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1057350271 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17860919 8103 RMVar_ID_8103 Human_SNP_ID_575505823 A-to-I Human chr15 - 44566906 44566906 44566906 CTGAGCTCAGGAGTTCAACACCAGCCTGGGCAACATGGTGCAATCCTGTCTCTACTAAAATACAA CTGAGCTCAGGAGTTCAACACCAGCCTGGGCATCATGGTGCAATCCTGTCTCTACTAAAATACAA T A SPG11 Ensembl:ENSG00000104133 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs996554964 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51212,RMVar_hsa_circ_57337,RMVar_hsa_circ_171616,RMVar_hsa_circ_100282,RMVar_hsa_circ_58416,RMVar_hsa_circ_110438,RMVar_hsa_circ_171617,RMVar_hsa_circ_88596,RMVar_hsa_circ_171618,RMVar_hsa_circ_23413,RMVar_hsa_circ_171619,RMVar_hsa_circ_70710,RMVar_hsa_circ_25392 8104 RMVar_ID_8104 Human_SNP_ID_575505842 A-to-I Human chr15 + 44566971 44566971 44566971 GCAATCCACCTACCTTGGCCTCCCAAAGTGCTAGGATTACAGGCATGAGCCACTGTGCCGGGCCA GCAATCCACCTACCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGTGCCGGGCCA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs972490763 Functional Loss SNV dbSNP153 33..33 33 - - - 8105 RMVar_ID_8105 Human_SNP_ID_575505888 A-to-I Human chr15 + 44567166 44567166 44567166 CAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATAGTCAAACCCCATCTCTATTAAAAATACAAA CAGGTCAGGAGTTCAAGACCAGCCTGGCCAACGTAGTCAAACCCCATCTCTATTAAAAATACAAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1385791752 Functional Loss SNV dbSNP153 33..33 33 - - - 8106 RMVar_ID_8106 Human_SNP_ID_575505912 A-to-I Human chr15 - 44567226 44567226 44567226 CCGCCTCAGCCTCCCAAGTAGCTGGGATTACAAGCACCTGCCACCACACCCGGCTAATTTTTTGT CCGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCACCTGCCACCACACCCGGCTAATTTTTTGT T C SPG11 Ensembl:ENSG00000104133 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1208850456 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51212,RMVar_hsa_circ_57337,RMVar_hsa_circ_171616,RMVar_hsa_circ_100282,RMVar_hsa_circ_58416,RMVar_hsa_circ_110438,RMVar_hsa_circ_171617,RMVar_hsa_circ_88596,RMVar_hsa_circ_171618,RMVar_hsa_circ_23413,RMVar_hsa_circ_171619,RMVar_hsa_circ_70710,RMVar_hsa_circ_25392 8107 RMVar_ID_8107 Human_SNP_ID_575508482 A-to-I Human chr15 - 44575627 44575627 44575627 AGCCAGGTGTGGTGGTGCACGCCTGTAATCCCAGCTACTCGAGAGGCTGAGGCACGAGAATCTAT AGCCAGGTGTGGTGGTGCACGCCTGTAATCCCTGCTACTCGAGAGGCTGAGGCACGAGAATCTAT T A SPG11 Ensembl:ENSG00000104133 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs991080761 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57337,RMVar_hsa_circ_171616,RMVar_hsa_circ_100282,RMVar_hsa_circ_58416,RMVar_hsa_circ_110438,RMVar_hsa_circ_171617,RMVar_hsa_circ_88596,RMVar_hsa_circ_171618,RMVar_hsa_circ_171619,RMVar_hsa_circ_70710,RMVar_hsa_circ_127373,RMVar_hsa_circ_17881,RMVar_hsa_circ_171623,RMVar_hsa_circ_94693,RMVar_hsa_circ_111664,RMVar_hsa_circ_171628,RMVar_hsa_circ_62997,RMVar_hsa_circ_350187,RMVar_hsa_circ_171629,RMVar_hsa_circ_377118,RMVar_hsa_circ_121255,RMVar_hsa_circ_171631,RMVar_hsa_circ_84688,RMVar_hsa_circ_171630,RMVar_hsa_circ_51500 8108 RMVar_ID_8108 Human_SNP_ID_575508590 A-to-I Human chr15 - 44576014 44576014 44576014 CCTCAGCCTCCTGAGTAGCTGGGATTACAGGCATGCGCCACCACACCCAGCTAACTTTAAATTTT CCTCAGCCTCCTGAGTAGCTGGGATTACAGGCGTGCGCCACCACACCCAGCTAACTTTAAATTTT T C SPG11 Ensembl:ENSG00000104133 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1478576689 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57337,RMVar_hsa_circ_171616,RMVar_hsa_circ_100282,RMVar_hsa_circ_58416,RMVar_hsa_circ_110438,RMVar_hsa_circ_171617,RMVar_hsa_circ_88596,RMVar_hsa_circ_171618,RMVar_hsa_circ_171619,RMVar_hsa_circ_70710,RMVar_hsa_circ_127373,RMVar_hsa_circ_17881,RMVar_hsa_circ_171623,RMVar_hsa_circ_94693,RMVar_hsa_circ_111664,RMVar_hsa_circ_171628,RMVar_hsa_circ_62997,RMVar_hsa_circ_350187,RMVar_hsa_circ_171629,RMVar_hsa_circ_377118,RMVar_hsa_circ_121255,RMVar_hsa_circ_171631,RMVar_hsa_circ_84688,RMVar_hsa_circ_171630,RMVar_hsa_circ_51500 8109 RMVar_ID_8109 Human_SNP_ID_575508709 A-to-I Human chr15 - 44576386 44576386 44576386 CCTCAGCCTCCCAAAGTGCTGGGGTTACAGGCATGAGCCACCACACCTGGCCTGACCCCCTTCTT CCTCAGCCTCCCAAAGTGCTGGGGTTACAGGCGTGAGCCACCACACCTGGCCTGACCCCCTTCTT T C SPG11 Ensembl:ENSG00000104133 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs943993011 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57337,RMVar_hsa_circ_171616,RMVar_hsa_circ_100282,RMVar_hsa_circ_58416,RMVar_hsa_circ_110438,RMVar_hsa_circ_171617,RMVar_hsa_circ_88596,RMVar_hsa_circ_171618,RMVar_hsa_circ_171619,RMVar_hsa_circ_70710,RMVar_hsa_circ_127373,RMVar_hsa_circ_17881,RMVar_hsa_circ_171623,RMVar_hsa_circ_94693,RMVar_hsa_circ_111664,RMVar_hsa_circ_171628,RMVar_hsa_circ_62997,RMVar_hsa_circ_350187,RMVar_hsa_circ_171629,RMVar_hsa_circ_377118,RMVar_hsa_circ_121255,RMVar_hsa_circ_171631,RMVar_hsa_circ_84688,RMVar_hsa_circ_171630,RMVar_hsa_circ_51500 8110 RMVar_ID_8110 Human_SNP_ID_575508869 A-to-I Human chr15 - 44576903 44576903 44576903 AGAATCGCTTGAACTCAGGAGGCAGAGGTTGCAGTGAACCGAGATGGTGCCACTGCACTCTAGCC AGAATCGCTTGAACTCAGGAGGCAGAGGTTGCGGTGAACCGAGATGGTGCCACTGCACTCTAGCC T C SPG11 Ensembl:ENSG00000104133 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1362074472 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12518351 RMVar_hsa_circ_57337,RMVar_hsa_circ_171616,RMVar_hsa_circ_100282,RMVar_hsa_circ_58416,RMVar_hsa_circ_110438,RMVar_hsa_circ_171617,RMVar_hsa_circ_88596,RMVar_hsa_circ_171618,RMVar_hsa_circ_171619,RMVar_hsa_circ_70710,RMVar_hsa_circ_127373,RMVar_hsa_circ_17881,RMVar_hsa_circ_171623,RMVar_hsa_circ_94693,RMVar_hsa_circ_111664,RMVar_hsa_circ_171628,RMVar_hsa_circ_62997,RMVar_hsa_circ_350187,RMVar_hsa_circ_171629,RMVar_hsa_circ_377118,RMVar_hsa_circ_121255,RMVar_hsa_circ_171631,RMVar_hsa_circ_84688,RMVar_hsa_circ_171630,RMVar_hsa_circ_51500 8111 RMVar_ID_8111 Human_SNP_ID_575508874 A-to-I Human chr15 - 44576912 44576912 44576912 TGAGGCAGGAGAATCGCTTGAACTCAGGAGGCAGAGGTTGCAGTGAACCGAGATGGTGCCACTGC TGAGGCAGGAGAATCGCTTGAACTCAGGAGGCTGAGGTTGCAGTGAACCGAGATGGTGCCACTGC T A SPG11 Ensembl:ENSG00000104133 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs544790188 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57337,RMVar_hsa_circ_171616,RMVar_hsa_circ_100282,RMVar_hsa_circ_58416,RMVar_hsa_circ_110438,RMVar_hsa_circ_171617,RMVar_hsa_circ_88596,RMVar_hsa_circ_171618,RMVar_hsa_circ_171619,RMVar_hsa_circ_70710,RMVar_hsa_circ_127373,RMVar_hsa_circ_17881,RMVar_hsa_circ_171623,RMVar_hsa_circ_94693,RMVar_hsa_circ_111664,RMVar_hsa_circ_171628,RMVar_hsa_circ_62997,RMVar_hsa_circ_350187,RMVar_hsa_circ_171629,RMVar_hsa_circ_377118,RMVar_hsa_circ_121255,RMVar_hsa_circ_171631,RMVar_hsa_circ_84688,RMVar_hsa_circ_171630,RMVar_hsa_circ_51500 8112 RMVar_ID_8112 Human_SNP_ID_575508875 A-to-I Human chr15 - 44576912 44576912 44576912 TGAGGCAGGAGAATCGCTTGAACTCAGGAGGCAGAGGTTGCAGTGAACCGAGATGGTGCCACTGC TGAGGCAGGAGAATCGCTTGAACTCAGGAGGCGGAGGTTGCAGTGAACCGAGATGGTGCCACTGC T C SPG11 Ensembl:ENSG00000104133 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs544790188 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57337,RMVar_hsa_circ_171616,RMVar_hsa_circ_100282,RMVar_hsa_circ_58416,RMVar_hsa_circ_110438,RMVar_hsa_circ_171617,RMVar_hsa_circ_88596,RMVar_hsa_circ_171618,RMVar_hsa_circ_171619,RMVar_hsa_circ_70710,RMVar_hsa_circ_127373,RMVar_hsa_circ_17881,RMVar_hsa_circ_171623,RMVar_hsa_circ_94693,RMVar_hsa_circ_111664,RMVar_hsa_circ_171628,RMVar_hsa_circ_62997,RMVar_hsa_circ_350187,RMVar_hsa_circ_171629,RMVar_hsa_circ_377118,RMVar_hsa_circ_121255,RMVar_hsa_circ_171631,RMVar_hsa_circ_84688,RMVar_hsa_circ_171630,RMVar_hsa_circ_51500 8113 RMVar_ID_8113 Human_SNP_ID_575508890 A-to-I Human chr15 - 44576991 44576991 44576991 AAACTTCATATCTACTAAAAATACAAAAAATTAGCTGGGCGTGGTGGTGCACACCCGTAATCCCA AAACTTCATATCTACTAAAAATACAAAAAATTGGCTGGGCGTGGTGGTGCACACCCGTAATCCCA T C SPG11 Ensembl:ENSG00000104133 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1402263799 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57337,RMVar_hsa_circ_171616,RMVar_hsa_circ_100282,RMVar_hsa_circ_58416,RMVar_hsa_circ_110438,RMVar_hsa_circ_171617,RMVar_hsa_circ_88596,RMVar_hsa_circ_171618,RMVar_hsa_circ_171619,RMVar_hsa_circ_70710,RMVar_hsa_circ_127373,RMVar_hsa_circ_17881,RMVar_hsa_circ_171623,RMVar_hsa_circ_94693,RMVar_hsa_circ_111664,RMVar_hsa_circ_171628,RMVar_hsa_circ_62997,RMVar_hsa_circ_350187,RMVar_hsa_circ_171629,RMVar_hsa_circ_377118,RMVar_hsa_circ_121255,RMVar_hsa_circ_171631,RMVar_hsa_circ_84688,RMVar_hsa_circ_171630,RMVar_hsa_circ_51500 8114 RMVar_ID_8114 Human_SNP_ID_575508994 A-to-I Human chr15 - 44577446 44577446 44577446 CAGGCTGGAGTGCAGTGGTGCAAACATGGCTCACTGCAGACTCAACCTCCAGGGCTCAAGCAGTC CAGGCTGGAGTGCAGTGGTGCAAACATGGCTCGCTGCAGACTCAACCTCCAGGGCTCAAGCAGTC T C SPG11 Ensembl:ENSG00000104133 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1367936767 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57337,RMVar_hsa_circ_171616,RMVar_hsa_circ_100282,RMVar_hsa_circ_58416,RMVar_hsa_circ_110438,RMVar_hsa_circ_171617,RMVar_hsa_circ_88596,RMVar_hsa_circ_171618,RMVar_hsa_circ_171619,RMVar_hsa_circ_70710,RMVar_hsa_circ_127373,RMVar_hsa_circ_17881,RMVar_hsa_circ_171623,RMVar_hsa_circ_94693,RMVar_hsa_circ_111664,RMVar_hsa_circ_171628,RMVar_hsa_circ_62997,RMVar_hsa_circ_350187,RMVar_hsa_circ_171629,RMVar_hsa_circ_377118,RMVar_hsa_circ_121255,RMVar_hsa_circ_171631,RMVar_hsa_circ_84688,RMVar_hsa_circ_171630,RMVar_hsa_circ_51500 8115 RMVar_ID_8115 Human_SNP_ID_575510376 A-to-I Human chr15 - 44582426 44582426 44582426 CGCCTGCCTCAGCCTCCCGAATAGCTGGGATTACAGGCGTGTACCACCACGCTTGGCTACTTTTT CGCCTGCCTCAGCCTCCCGAATAGCTGGGATTGCAGGCGTGTACCACCACGCTTGGCTACTTTTT T C SPG11 Ensembl:ENSG00000104133 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs961661845 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57337,RMVar_hsa_circ_171616,RMVar_hsa_circ_100282,RMVar_hsa_circ_58416,RMVar_hsa_circ_110438,RMVar_hsa_circ_171617,RMVar_hsa_circ_88596,RMVar_hsa_circ_171618,RMVar_hsa_circ_171619,RMVar_hsa_circ_70710,RMVar_hsa_circ_127373,RMVar_hsa_circ_17881,RMVar_hsa_circ_171623,RMVar_hsa_circ_94693,RMVar_hsa_circ_111664,RMVar_hsa_circ_171628,RMVar_hsa_circ_62997,RMVar_hsa_circ_350187,RMVar_hsa_circ_171629,RMVar_hsa_circ_377118,RMVar_hsa_circ_121255,RMVar_hsa_circ_171631,RMVar_hsa_circ_84688,RMVar_hsa_circ_171630,RMVar_hsa_circ_51500 8116 RMVar_ID_8116 Human_SNP_ID_575510603 A-to-I Human chr15 - 44583314 44583314 44583314 AGCTGGGATTACTGGCTAATTTTTGTATTAGTAGAGACCGGGTTTCACCATGTTGGCCAGGCTGG AGCTGGGATTACTGGCTAATTTTTGTATTAGTGGAGACCGGGTTTCACCATGTTGGCCAGGCTGG T C SPG11 Ensembl:ENSG00000104133 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs545120319 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12518450 RMVar_hsa_circ_57337,RMVar_hsa_circ_171616,RMVar_hsa_circ_100282,RMVar_hsa_circ_58416,RMVar_hsa_circ_110438,RMVar_hsa_circ_171617,RMVar_hsa_circ_88596,RMVar_hsa_circ_171618,RMVar_hsa_circ_171619,RMVar_hsa_circ_70710,RMVar_hsa_circ_127373,RMVar_hsa_circ_17881,RMVar_hsa_circ_171623,RMVar_hsa_circ_94693,RMVar_hsa_circ_111664,RMVar_hsa_circ_171628,RMVar_hsa_circ_62997,RMVar_hsa_circ_350187,RMVar_hsa_circ_171629,RMVar_hsa_circ_377118,RMVar_hsa_circ_121255,RMVar_hsa_circ_171631,RMVar_hsa_circ_84688,RMVar_hsa_circ_171630,RMVar_hsa_circ_51500 8117 RMVar_ID_8117 Human_SNP_ID_575515756 A-to-I Human chr15 - 44600919 44600919 44600919 CAACTCTTGACCTCAGGTCATCCGCCTGCCTTAGTCTCCCAAAGTGCTGGGATTACAGGCGTGAG CAACTCTTGACCTCAGGTCATCCGCCTGCCTTCGTCTCCCAAAGTGCTGGGATTACAGGCGTGAG T G SPG11 Ensembl:ENSG00000104133 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs566692520 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12817,RMVar_hsa_circ_110438,RMVar_hsa_circ_88596,RMVar_hsa_circ_171618,RMVar_hsa_circ_171619,RMVar_hsa_circ_48341,RMVar_hsa_circ_62997,RMVar_hsa_circ_171631,RMVar_hsa_circ_84688,RMVar_hsa_circ_356103,RMVar_hsa_circ_342215,RMVar_hsa_circ_11365,RMVar_hsa_circ_324202,RMVar_hsa_circ_171639,RMVar_hsa_circ_171640,RMVar_hsa_circ_30561,RMVar_hsa_circ_351325,RMVar_hsa_circ_171642,RMVar_hsa_circ_321065,RMVar_hsa_circ_346008,RMVar_hsa_circ_376388,RMVar_hsa_circ_38330,RMVar_hsa_circ_171645,RMVar_hsa_circ_171643,RMVar_hsa_circ_171644,RMVar_hsa_circ_322222,RMVar_hsa_circ_92348,RMVar_hsa_circ_30058,RMVar_hsa_circ_171652,RMVar_hsa_circ_27965,RMVar_hsa_circ_321959,RMVar_hsa_circ_4756,RMVar_hsa_circ_328778,RMVar_hsa_circ_340315,RMVar_hsa_circ_323140,RMVar_hsa_circ_114809,RMVar_hsa_circ_284541,RMVar_hsa_circ_37659,RMVar_hsa_circ_171655,RMVar_hsa_circ_171657,RMVar_hsa_circ_171658,RMVar_hsa_circ_171656,RMVar_hsa_circ_171654 8118 RMVar_ID_8118 Human_SNP_ID_575515806 A-to-I Human chr15 - 44601113 44601113 44601113 AGTTTCACTCTTGTTGCCCAGGCTGGAGTGCAATGGCGCGATCTTGGCTCACCACAACCTCTGCC AGTTTCACTCTTGTTGCCCAGGCTGGAGTGCAGTGGCGCGATCTTGGCTCACCACAACCTCTGCC T C SPG11 Ensembl:ENSG00000104133 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1044569237 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12817,RMVar_hsa_circ_110438,RMVar_hsa_circ_88596,RMVar_hsa_circ_171618,RMVar_hsa_circ_171619,RMVar_hsa_circ_48341,RMVar_hsa_circ_62997,RMVar_hsa_circ_171631,RMVar_hsa_circ_84688,RMVar_hsa_circ_356103,RMVar_hsa_circ_342215,RMVar_hsa_circ_11365,RMVar_hsa_circ_324202,RMVar_hsa_circ_171639,RMVar_hsa_circ_171640,RMVar_hsa_circ_30561,RMVar_hsa_circ_351325,RMVar_hsa_circ_171642,RMVar_hsa_circ_321065,RMVar_hsa_circ_346008,RMVar_hsa_circ_376388,RMVar_hsa_circ_38330,RMVar_hsa_circ_171645,RMVar_hsa_circ_171643,RMVar_hsa_circ_171644,RMVar_hsa_circ_322222,RMVar_hsa_circ_92348,RMVar_hsa_circ_30058,RMVar_hsa_circ_171652,RMVar_hsa_circ_27965,RMVar_hsa_circ_321959,RMVar_hsa_circ_4756,RMVar_hsa_circ_328778,RMVar_hsa_circ_340315,RMVar_hsa_circ_323140,RMVar_hsa_circ_114809,RMVar_hsa_circ_284541,RMVar_hsa_circ_37659,RMVar_hsa_circ_171655,RMVar_hsa_circ_171657,RMVar_hsa_circ_171658,RMVar_hsa_circ_171656,RMVar_hsa_circ_171654 8119 RMVar_ID_8119 Human_SNP_ID_575515987 A-to-I Human chr15 - 44601674 44601674 44601674 CGTGCCTCTAAGTCCTAGCTACTTAGGAGGCTAAGGCAGGAGAATCACTTGAACCCAGGAGGCGG CGTGCCTCTAAGTCCTAGCTACTTAGGAGGCTGAGGCAGGAGAATCACTTGAACCCAGGAGGCGG T C SPG11 Ensembl:ENSG00000104133 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1471871677 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12817,RMVar_hsa_circ_110438,RMVar_hsa_circ_88596,RMVar_hsa_circ_171618,RMVar_hsa_circ_171619,RMVar_hsa_circ_48341,RMVar_hsa_circ_62997,RMVar_hsa_circ_171631,RMVar_hsa_circ_84688,RMVar_hsa_circ_356103,RMVar_hsa_circ_342215,RMVar_hsa_circ_11365,RMVar_hsa_circ_324202,RMVar_hsa_circ_171639,RMVar_hsa_circ_171640,RMVar_hsa_circ_30561,RMVar_hsa_circ_351325,RMVar_hsa_circ_171642,RMVar_hsa_circ_321065,RMVar_hsa_circ_346008,RMVar_hsa_circ_376388,RMVar_hsa_circ_38330,RMVar_hsa_circ_171645,RMVar_hsa_circ_171643,RMVar_hsa_circ_171644,RMVar_hsa_circ_322222,RMVar_hsa_circ_92348,RMVar_hsa_circ_30058,RMVar_hsa_circ_171652,RMVar_hsa_circ_27965,RMVar_hsa_circ_321959,RMVar_hsa_circ_4756,RMVar_hsa_circ_328778,RMVar_hsa_circ_340315,RMVar_hsa_circ_323140,RMVar_hsa_circ_114809,RMVar_hsa_circ_284541,RMVar_hsa_circ_37659,RMVar_hsa_circ_171655,RMVar_hsa_circ_171657,RMVar_hsa_circ_171658,RMVar_hsa_circ_171656,RMVar_hsa_circ_171654 8120 RMVar_ID_8120 Human_SNP_ID_575523638 A-to-I Human chr15 - 44630853 44630853 44630853 CATTCTCAGACTGGGTGCAGTGTCTCACGCCTATGATCCCAGCACTTTGGGAGGCCGAGATGGGT CATTCTCAGACTGGGTGCAGTGTCTCACGCCTCTGATCCCAGCACTTTGGGAGGCCGAGATGGGT T G SPG11 Ensembl:ENSG00000104133 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs116654021 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12817,RMVar_hsa_circ_88596,RMVar_hsa_circ_171619,RMVar_hsa_circ_30058,RMVar_hsa_circ_24945,RMVar_hsa_circ_27965,RMVar_hsa_circ_323140,RMVar_hsa_circ_284541,RMVar_hsa_circ_171655,RMVar_hsa_circ_171654,RMVar_hsa_circ_42234,RMVar_hsa_circ_320602,RMVar_hsa_circ_60873,RMVar_hsa_circ_192,RMVar_hsa_circ_370229,RMVar_hsa_circ_171666,RMVar_hsa_circ_350670,RMVar_hsa_circ_329662,RMVar_hsa_circ_171671,RMVar_hsa_circ_42722,RMVar_hsa_circ_54497,RMVar_hsa_circ_171672,RMVar_hsa_circ_325985,RMVar_hsa_circ_291751,RMVar_hsa_circ_316551,RMVar_hsa_circ_309337,RMVar_hsa_circ_171678,RMVar_hsa_circ_171675,RMVar_hsa_circ_171676,RMVar_hsa_circ_171677,RMVar_hsa_circ_171674,RMVar_hsa_circ_32752,RMVar_hsa_circ_295652,RMVar_hsa_circ_326215,RMVar_hsa_circ_38969,RMVar_hsa_circ_171679 8121 RMVar_ID_8121 Human_SNP_ID_575524942 A-to-I Human chr15 - 44635392 44635392 44635392 TACTAAAACCTTTTTAGAAACAAGGTCTCACTATGTTGCCCAGGCTGGTCTCAAACTCCTGGGCT TACTAAAACCTTTTTAGAAACAAGGTCTCACTGTGTTGCCCAGGCTGGTCTCAAACTCCTGGGCT T C SPG11 Ensembl:ENSG00000104133 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs907428558 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12817,RMVar_hsa_circ_88596,RMVar_hsa_circ_171619,RMVar_hsa_circ_30058,RMVar_hsa_circ_24945,RMVar_hsa_circ_323140,RMVar_hsa_circ_284541,RMVar_hsa_circ_171655,RMVar_hsa_circ_171654,RMVar_hsa_circ_320602,RMVar_hsa_circ_192,RMVar_hsa_circ_370229,RMVar_hsa_circ_171666,RMVar_hsa_circ_350670,RMVar_hsa_circ_329662,RMVar_hsa_circ_171671,RMVar_hsa_circ_42722,RMVar_hsa_circ_171672,RMVar_hsa_circ_325985,RMVar_hsa_circ_291751,RMVar_hsa_circ_316551,RMVar_hsa_circ_171678,RMVar_hsa_circ_171675,RMVar_hsa_circ_171676,RMVar_hsa_circ_171677,RMVar_hsa_circ_32752,RMVar_hsa_circ_295652,RMVar_hsa_circ_38969,RMVar_hsa_circ_171679,RMVar_hsa_circ_171682,RMVar_hsa_circ_265268,RMVar_hsa_circ_309350,RMVar_hsa_circ_311246,RMVar_hsa_circ_321266,RMVar_hsa_circ_293475,RMVar_hsa_circ_171684,RMVar_hsa_circ_171683,RMVar_hsa_circ_171681 8122 RMVar_ID_8122 Human_SNP_ID_575528927 A-to-I Human chr15 - 44650268 44650268 44650268 GTGATCATCCCGGCTTGGCCTCCCAAAGTGCTAGGATTACAGGCGTGAGCCACCATGCTTAGCCT GTGATCATCCCGGCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCATGCTTAGCCT T C SPG11 Ensembl:ENSG00000104133 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1173248880 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12817,RMVar_hsa_circ_88596,RMVar_hsa_circ_171619,RMVar_hsa_circ_30058,RMVar_hsa_circ_323140,RMVar_hsa_circ_284541,RMVar_hsa_circ_171655,RMVar_hsa_circ_171654,RMVar_hsa_circ_320602,RMVar_hsa_circ_192,RMVar_hsa_circ_370229,RMVar_hsa_circ_171666,RMVar_hsa_circ_350670,RMVar_hsa_circ_329662,RMVar_hsa_circ_171671,RMVar_hsa_circ_171672,RMVar_hsa_circ_325985,RMVar_hsa_circ_291751,RMVar_hsa_circ_316551,RMVar_hsa_circ_85176,RMVar_hsa_circ_171678,RMVar_hsa_circ_171675,RMVar_hsa_circ_171676,RMVar_hsa_circ_171677,RMVar_hsa_circ_32752,RMVar_hsa_circ_295652,RMVar_hsa_circ_171679,RMVar_hsa_circ_171682,RMVar_hsa_circ_265268,RMVar_hsa_circ_309350,RMVar_hsa_circ_321266,RMVar_hsa_circ_293475,RMVar_hsa_circ_171684,RMVar_hsa_circ_171683,RMVar_hsa_circ_117389,RMVar_hsa_circ_290661,RMVar_hsa_circ_303400,RMVar_hsa_circ_171687,RMVar_hsa_circ_171689,RMVar_hsa_circ_171690,RMVar_hsa_circ_171688,RMVar_hsa_circ_171686 8123 RMVar_ID_8123 Human_SNP_ID_575528994 A-to-I Human chr15 - 44650506 44650506 44650506 GGGACCACAGGCACGCACCACCACTCCCAGCTAATTTTTGTATTTTTAGTAGAGACGACGTCTCG GGGACCACAGGCACGCACCACCACTCCCAGCTGATTTTTGTATTTTTAGTAGAGACGACGTCTCG T C SPG11 Ensembl:ENSG00000104133 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1235726715 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12817,RMVar_hsa_circ_88596,RMVar_hsa_circ_171619,RMVar_hsa_circ_30058,RMVar_hsa_circ_323140,RMVar_hsa_circ_284541,RMVar_hsa_circ_171655,RMVar_hsa_circ_171654,RMVar_hsa_circ_320602,RMVar_hsa_circ_192,RMVar_hsa_circ_370229,RMVar_hsa_circ_171666,RMVar_hsa_circ_350670,RMVar_hsa_circ_329662,RMVar_hsa_circ_171671,RMVar_hsa_circ_171672,RMVar_hsa_circ_325985,RMVar_hsa_circ_291751,RMVar_hsa_circ_316551,RMVar_hsa_circ_85176,RMVar_hsa_circ_171678,RMVar_hsa_circ_171675,RMVar_hsa_circ_171676,RMVar_hsa_circ_171677,RMVar_hsa_circ_32752,RMVar_hsa_circ_295652,RMVar_hsa_circ_171679,RMVar_hsa_circ_171682,RMVar_hsa_circ_265268,RMVar_hsa_circ_309350,RMVar_hsa_circ_321266,RMVar_hsa_circ_293475,RMVar_hsa_circ_171684,RMVar_hsa_circ_171683,RMVar_hsa_circ_117389,RMVar_hsa_circ_290661,RMVar_hsa_circ_303400,RMVar_hsa_circ_171687,RMVar_hsa_circ_171689,RMVar_hsa_circ_171690,RMVar_hsa_circ_171688,RMVar_hsa_circ_171686 8124 RMVar_ID_8124 Human_SNP_ID_575531109 A-to-I Human chr15 - 44657970 44657970 44657970 CAGGCTGGAGTGCAGTGGCGTGATCTCGGCTCACTGCAACCCCTGCCTCCTGGGCTCAAGCGATT CAGGCTGGAGTGCAGTGGCGTGATCTCGGCTCTCTGCAACCCCTGCCTCCTGGGCTCAAGCGATT T A SPG11 Ensembl:ENSG00000104133 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs997697012 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12817,RMVar_hsa_circ_30058,RMVar_hsa_circ_323140,RMVar_hsa_circ_284541,RMVar_hsa_circ_171654,RMVar_hsa_circ_320602,RMVar_hsa_circ_192,RMVar_hsa_circ_370229,RMVar_hsa_circ_171666,RMVar_hsa_circ_329662,RMVar_hsa_circ_171672,RMVar_hsa_circ_325985,RMVar_hsa_circ_291751,RMVar_hsa_circ_316551,RMVar_hsa_circ_85176,RMVar_hsa_circ_171678,RMVar_hsa_circ_171676,RMVar_hsa_circ_171677,RMVar_hsa_circ_295652,RMVar_hsa_circ_309350,RMVar_hsa_circ_293475,RMVar_hsa_circ_171684,RMVar_hsa_circ_171683,RMVar_hsa_circ_303400,RMVar_hsa_circ_126301,RMVar_hsa_circ_171687,RMVar_hsa_circ_171686,RMVar_hsa_circ_295205,RMVar_hsa_circ_171693,RMVar_hsa_circ_88863,RMVar_hsa_circ_310631,RMVar_hsa_circ_171692,RMVar_hsa_circ_171694 8125 RMVar_ID_8125 Human_SNP_ID_575549626 A-to-I Human chr15 + 44733100 44733100 44733100 CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCACCCACCACCACGCCCCGCTAATTTTT CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTGCAGGCACCCACCACCACGCCCCGCTAATTTTT A G TRIM69 Ensembl:ENSG00000185880 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1017282212 Functional Loss SNV dbSNP153 33..33 33 - - - 8126 RMVar_ID_8126 Human_SNP_ID_575549783 A-to-I Human chr15 + 44733526 44733526 44733526 CAGCCTGGCCAACATGGCAAAACCCCGTCTCTACTAAAAATACAAAATTAGCTGAGTGTGGTGGT CAGCCTGGCCAACATGGCAAAACCCCGTCTCTCCTAAAAATACAAAATTAGCTGAGTGTGGTGGT A C TRIM69 Ensembl:ENSG00000185880 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1453276569 Functional Loss SNV dbSNP153 33..33 33 - - - 8127 RMVar_ID_8127 Human_SNP_ID_695542277 A-to-I Human chr21 + 41173652 41173652 41173652 TCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAACCTGGGAGGCAAAGGTT TCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCGGGAGAATTGCTTGAACCTGGGAGGCAAAGGTT A G BACE2 Ensembl:ENSG00000182240 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1172228161 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84580,RMVar_hsa_circ_212361 8128 RMVar_ID_8128 Human_SNP_ID_695542464 A-to-I Human chr21 + 41174196 41174196 41174196 TAAACAGTCTCGCTCTGTTGCCAGGCTGGAGTACAGTGGCCTGATCTTGGCTCACTGCAACCTCC TAAACAGTCTCGCTCTGTTGCCAGGCTGGAGTGCAGTGGCCTGATCTTGGCTCACTGCAACCTCC A G BACE2 Ensembl:ENSG00000182240 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1211546376 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84580,RMVar_hsa_circ_212361 8129 RMVar_ID_8129 Human_SNP_ID_695542527 A-to-I Human chr21 + 41174409 41174409 41174409 GTGATCTGCCCACCTCGGCCTCCCAAAGTGCTAGGATTACAGGCGTGAGCCACCGCGCGGCCAAG GTGATCTGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCGGCCAAG A G BACE2 Ensembl:ENSG00000182240 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs953215997 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84580,RMVar_hsa_circ_212361 8130 RMVar_ID_8130 Human_SNP_ID_695551850 A-to-I Human chr21 + 41213631 41213631 41213631 CCCGTCTCTACTAAAATACAAAAAAATTAGCCAGGCTTGGTGGTGGGTGCCTGTAGTCCCAGCTA CCCGTCTCTACTAAAATACAAAAAAATTAGCCGGGCTTGGTGGTGGGTGCCTGTAGTCCCAGCTA A G BACE2 Ensembl:ENSG00000182240 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1363588623 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84580,RMVar_hsa_circ_212361 8131 RMVar_ID_8131 Human_SNP_ID_695553886 A-to-I Human chr21 + 41221748 41221748 41221748 TACTCGGGAGGCTGAGGCAGGAGAATGGCGTGAGCCCAGGAGGAGGAGCTTGCAGTGAGCTGAGA TACTCGGGAGGCTGAGGCAGGAGAATGGCGTGGGCCCAGGAGGAGGAGCTTGCAGTGAGCTGAGA A G BACE2 Ensembl:ENSG00000182240 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1226327313 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84580,RMVar_hsa_circ_212361 8132 RMVar_ID_8132 Human_SNP_ID_695554296 A-to-I Human chr21 + 41223076 41223076 41223076 AAACTGAGAGCTGAAAACAACAGGAATGGGCCAGGTGCAGTGGCTCATGCCTGTAATCCCAGCAC AAACTGAGAGCTGAAAACAACAGGAATGGGCCGGGTGCAGTGGCTCATGCCTGTAATCCCAGCAC A G BACE2 Ensembl:ENSG00000182240 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1364350680 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84580,RMVar_hsa_circ_212361 8133 RMVar_ID_8133 Human_SNP_ID_695554645 A-to-I Human chr21 + 41224380 41224380 41224380 GGGACTGCAGGCGTGTGCCACCACGTCCGGCTAATTTTTTGTATTTTTAGTAGAGATGGGGTTTC GGGACTGCAGGCGTGTGCCACCACGTCCGGCTGATTTTTTGTATTTTTAGTAGAGATGGGGTTTC A G BACE2 Ensembl:ENSG00000182240 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1490683877 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84580,RMVar_hsa_circ_212361 8134 RMVar_ID_8134 Human_SNP_ID_695554660 A-to-I Human chr21 + 41224450 41224450 41224450 GTTAGCCAGGATCCACTCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGTGC GTTAGCCAGGATCCACTCACCTCGGCCTCCCACAGTGCTGGGATTACAGGCGTGAGCCACTGTGC A C BACE2 Ensembl:ENSG00000182240 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs747293434 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84580,RMVar_hsa_circ_212361 8135 RMVar_ID_8135 Human_SNP_ID_695554799 A-to-I Human chr21 + 41224979 41224979 41224979 CTAGTCGGCTGGGTGCGGTGGCTCACGCCTGTAATCCCAGCACCTTGGGAGGCCGAGGCGGGCAG CTAGTCGGCTGGGTGCGGTGGCTCACGCCTGTGATCCCAGCACCTTGGGAGGCCGAGGCGGGCAG A G BACE2 Ensembl:ENSG00000182240 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1298675239 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84580,RMVar_hsa_circ_212361 8136 RMVar_ID_8136 Human_SNP_ID_695555681 A-to-I Human chr21 + 41228411 41228411 41228411 TTAGACTGTTGTGCTGCTATAAGAGAATACCCAAGGCTGGGGAGTTTATAAAGAAAAGAGGTTTA TTAGACTGTTGTGCTGCTATAAGAGAATACCCGAGGCTGGGGAGTTTATAAAGAAAAGAGGTTTA A G BACE2 Ensembl:ENSG00000182240 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs993708482 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_212362,RMVar_hsa_circ_357499,RMVar_hsa_circ_372978,RMVar_hsa_circ_126652,RMVar_hsa_circ_298531,RMVar_hsa_circ_212363,RMVar_hsa_circ_212364 8137 RMVar_ID_8137 Human_SNP_ID_695556624 A-to-I Human chr21 + 41232760 41232760 41232760 CTCACCAGAAGCAGATGCCAGCAACATGCTTCATGCACAGCCTACAGAACCATGAGCCAAAATCA CTCACCAGAAGCAGATGCCAGCAACATGCTTCCTGCACAGCCTACAGAACCATGAGCCAAAATCA A C BACE2 Ensembl:ENSG00000182240 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1450602688 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_212362,RMVar_hsa_circ_357499,RMVar_hsa_circ_372978,RMVar_hsa_circ_126652,RMVar_hsa_circ_298531,RMVar_hsa_circ_212363,RMVar_hsa_circ_212364 8138 RMVar_ID_8138 Human_SNP_ID_695566812 A-to-I Human chr21 + 41275378 41275378 41275378 GGATTTTCCCTTTCTGTCTCCCCAGAAATTGCAGGTGCTGCAGTGTCTGAAATTTCCGGGCCTTT GGATTTTCCCTTTCTGTCTCCCCAGAAATTGCTGGTGCTGCAGTGTCTGAAATTTCCGGGCCTTT A T BACE2 Ensembl:ENSG00000182240 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1233883847 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_572666 Human_Splice_Rec_2123810,Human_Splice_Rec_2123824,Human_Splice_Rec_2123840,Human_Splice_Rec_2123860,Human_Splice_Rec_2123880,Human_Splice_Rec_2123902 8139 RMVar_ID_8139 Human_SNP_ID_695604977 A-to-I Human chr21 + 41429857 41429851 41429858 TTGAACCCGGGAGGTGGAGGTTGCAGTGAGCCAAGATTGCGCCACTGCTCTCCAGCCTGGTGACA TTGAACCCGGGAGGTGGAGGTTGCAGT_______GATTGCGCCACTGCTCTCCAGCCTGGTGACA TGAGCCAA T MX1 Ensembl:ENSG00000157601 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1235233280 Functional Loss DEL dbSNP153 28..34 33 - - - RMVar_hsa_circ_212377,RMVar_hsa_circ_72250,RMVar_hsa_circ_212379,RMVar_hsa_circ_79996,RMVar_hsa_circ_82123,RMVar_hsa_circ_87703,RMVar_hsa_circ_212382,RMVar_hsa_circ_212383,RMVar_hsa_circ_77251,RMVar_hsa_circ_212384,RMVar_hsa_circ_98106,RMVar_hsa_circ_212385 8140 RMVar_ID_8140 Human_SNP_ID_695609860 A-to-I Human chr21 + 41448542 41448542 41448542 TAAGAAGGGGTCTTGGCCGGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAG TAAGAAGGGGTCTTGGCCGGGCACGGTGGCTCCCGCCTGTAATCCCAGCACTTTGGGAGGCCGAG A C MX1 Ensembl:ENSG00000157601 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs895930378 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82123,RMVar_hsa_circ_87703,RMVar_hsa_circ_212382,RMVar_hsa_circ_212384,RMVar_hsa_circ_98106,RMVar_hsa_circ_212385,RMVar_hsa_circ_105600,RMVar_hsa_circ_125265,RMVar_hsa_circ_212386,RMVar_hsa_circ_115764,RMVar_hsa_circ_212387,RMVar_hsa_circ_73059,RMVar_hsa_circ_84036,RMVar_hsa_circ_212388,RMVar_hsa_circ_212389,RMVar_hsa_circ_60703,RMVar_hsa_circ_104830,RMVar_hsa_circ_322561,RMVar_hsa_circ_212391 8141 RMVar_ID_8141 Human_SNP_ID_695609861 A-to-I Human chr21 + 41448542 41448542 41448542 TAAGAAGGGGTCTTGGCCGGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAG TAAGAAGGGGTCTTGGCCGGGCACGGTGGCTCGCGCCTGTAATCCCAGCACTTTGGGAGGCCGAG A G MX1 Ensembl:ENSG00000157601 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs895930378 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82123,RMVar_hsa_circ_87703,RMVar_hsa_circ_212382,RMVar_hsa_circ_212384,RMVar_hsa_circ_98106,RMVar_hsa_circ_212385,RMVar_hsa_circ_105600,RMVar_hsa_circ_125265,RMVar_hsa_circ_212386,RMVar_hsa_circ_115764,RMVar_hsa_circ_212387,RMVar_hsa_circ_73059,RMVar_hsa_circ_84036,RMVar_hsa_circ_212388,RMVar_hsa_circ_212389,RMVar_hsa_circ_60703,RMVar_hsa_circ_104830,RMVar_hsa_circ_322561,RMVar_hsa_circ_212391 8142 RMVar_ID_8142 Human_SNP_ID_695609862 A-to-I Human chr21 + 41448542 41448542 41448542 TAAGAAGGGGTCTTGGCCGGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAG TAAGAAGGGGTCTTGGCCGGGCACGGTGGCTCTCGCCTGTAATCCCAGCACTTTGGGAGGCCGAG A T MX1 Ensembl:ENSG00000157601 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs895930378 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82123,RMVar_hsa_circ_87703,RMVar_hsa_circ_212382,RMVar_hsa_circ_212384,RMVar_hsa_circ_98106,RMVar_hsa_circ_212385,RMVar_hsa_circ_105600,RMVar_hsa_circ_125265,RMVar_hsa_circ_212386,RMVar_hsa_circ_115764,RMVar_hsa_circ_212387,RMVar_hsa_circ_73059,RMVar_hsa_circ_84036,RMVar_hsa_circ_212388,RMVar_hsa_circ_212389,RMVar_hsa_circ_60703,RMVar_hsa_circ_104830,RMVar_hsa_circ_322561,RMVar_hsa_circ_212391 8143 RMVar_ID_8143 Human_SNP_ID_695611895 A-to-I Human chr21 + 41456058 41456058 41456058 GAGGCCAGGAGTTTGAGACCAGCCTGGCCAACATGGCGAAACCCGGTCTCTACTAAAAATACAAA GAGGCCAGGAGTTTGAGACCAGCCTGGCCAACGTGGCGAAACCCGGTCTCTACTAAAAATACAAA A G MX1 Ensembl:ENSG00000157601 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1387701420 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82123,RMVar_hsa_circ_87703,RMVar_hsa_circ_212382,RMVar_hsa_circ_212384,RMVar_hsa_circ_98106,RMVar_hsa_circ_212385,RMVar_hsa_circ_105600,RMVar_hsa_circ_125265,RMVar_hsa_circ_212386,RMVar_hsa_circ_115764,RMVar_hsa_circ_212387,RMVar_hsa_circ_84036,RMVar_hsa_circ_212388,RMVar_hsa_circ_212389,RMVar_hsa_circ_104830,RMVar_hsa_circ_212391,RMVar_hsa_circ_123492,RMVar_hsa_circ_212392 8144 RMVar_ID_8144 Human_SNP_ID_695611899 A-to-I Human chr21 + 41456064 41456064 41456064 AGGAGTTTGAGACCAGCCTGGCCAACATGGCGAAACCCGGTCTCTACTAAAAATACAAAAAAATT AGGAGTTTGAGACCAGCCTGGCCAACATGGCGGAACCCGGTCTCTACTAAAAATACAAAAAAATT A G MX1 Ensembl:ENSG00000157601 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs770410462 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82123,RMVar_hsa_circ_87703,RMVar_hsa_circ_212382,RMVar_hsa_circ_212384,RMVar_hsa_circ_98106,RMVar_hsa_circ_212385,RMVar_hsa_circ_105600,RMVar_hsa_circ_125265,RMVar_hsa_circ_212386,RMVar_hsa_circ_115764,RMVar_hsa_circ_212387,RMVar_hsa_circ_84036,RMVar_hsa_circ_212388,RMVar_hsa_circ_212389,RMVar_hsa_circ_104830,RMVar_hsa_circ_212391,RMVar_hsa_circ_123492,RMVar_hsa_circ_212392 8145 RMVar_ID_8145 Human_SNP_ID_695611907 A-to-I Human chr21 + 41456080 41456080 41456080 CCTGGCCAACATGGCGAAACCCGGTCTCTACTAAAAATACAAAAAAATTAGCTGTGCATGGTGGC CCTGGCCAACATGGCGAAACCCGGTCTCTACTGAAAATACAAAAAAATTAGCTGTGCATGGTGGC A G MX1 Ensembl:ENSG00000157601 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1014499437 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82123,RMVar_hsa_circ_87703,RMVar_hsa_circ_212382,RMVar_hsa_circ_212384,RMVar_hsa_circ_98106,RMVar_hsa_circ_212385,RMVar_hsa_circ_105600,RMVar_hsa_circ_125265,RMVar_hsa_circ_212386,RMVar_hsa_circ_115764,RMVar_hsa_circ_212387,RMVar_hsa_circ_84036,RMVar_hsa_circ_212388,RMVar_hsa_circ_212389,RMVar_hsa_circ_104830,RMVar_hsa_circ_212391,RMVar_hsa_circ_123492,RMVar_hsa_circ_212392 8146 RMVar_ID_8146 Human_SNP_ID_695611921 A-to-I Human chr21 + 41456121 41456121 41456121 AAAAAATTAGCTGTGCATGGTGGCCCATGCCTATAGTCCCAGCTACTTGGGAAGCTGAGATATGA AAAAAATTAGCTGTGCATGGTGGCCCATGCCTGTAGTCCCAGCTACTTGGGAAGCTGAGATATGA A G MX1 Ensembl:ENSG00000157601 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs901692997 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82123,RMVar_hsa_circ_87703,RMVar_hsa_circ_212382,RMVar_hsa_circ_212384,RMVar_hsa_circ_98106,RMVar_hsa_circ_212385,RMVar_hsa_circ_105600,RMVar_hsa_circ_125265,RMVar_hsa_circ_212386,RMVar_hsa_circ_115764,RMVar_hsa_circ_212387,RMVar_hsa_circ_84036,RMVar_hsa_circ_212388,RMVar_hsa_circ_212389,RMVar_hsa_circ_104830,RMVar_hsa_circ_212391,RMVar_hsa_circ_123492,RMVar_hsa_circ_212392 8147 RMVar_ID_8147 Human_SNP_ID_695611988 A-to-I Human chr21 + 41456379 41456379 41456379 GCAAGTCCAAAATCCCAGGGCAGGCCAGCAGGAAGAGCAGGCCAGAAATTGCAGCAGGAGCTAAG GCAAGTCCAAAATCCCAGGGCAGGCCAGCAGGGAGAGCAGGCCAGAAATTGCAGCAGGAGCTAAG A G MX1 Ensembl:ENSG00000157601 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs386760 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82123,RMVar_hsa_circ_87703,RMVar_hsa_circ_212382,RMVar_hsa_circ_212384,RMVar_hsa_circ_98106,RMVar_hsa_circ_212385,RMVar_hsa_circ_105600,RMVar_hsa_circ_125265,RMVar_hsa_circ_212386,RMVar_hsa_circ_115764,RMVar_hsa_circ_212387,RMVar_hsa_circ_84036,RMVar_hsa_circ_212388,RMVar_hsa_circ_212389,RMVar_hsa_circ_104830,RMVar_hsa_circ_212391,RMVar_hsa_circ_123492,RMVar_hsa_circ_212392 8148 RMVar_ID_8148 Human_SNP_ID_695612098 A-to-I Human chr21 + 41456879 41456879 41456879 TGCATCCTGAGATCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCACGTG TGCATCCTGAGATCAAGCGATTCTCCTGCCTCGGCCTCCTGAGTAGCTGGGACTACAGGCACGTG A G MX1 Ensembl:ENSG00000157601 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1345409759 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82123,RMVar_hsa_circ_87703,RMVar_hsa_circ_212382,RMVar_hsa_circ_212384,RMVar_hsa_circ_98106,RMVar_hsa_circ_212385,RMVar_hsa_circ_105600,RMVar_hsa_circ_125265,RMVar_hsa_circ_212386,RMVar_hsa_circ_115764,RMVar_hsa_circ_212387,RMVar_hsa_circ_84036,RMVar_hsa_circ_212388,RMVar_hsa_circ_212389,RMVar_hsa_circ_104830,RMVar_hsa_circ_212391,RMVar_hsa_circ_123492,RMVar_hsa_circ_212392 8149 RMVar_ID_8149 Human_SNP_ID_695612857 A-to-I Human chr21 + 41459716 41459716 41459716 CTACTCAGGAGGCTGAGACATGAGAATTGCTTAAACCCGGGAGGTGGAGGTTGCAGTGAGCCCAG CTACTCAGGAGGCTGAGACATGAGAATTGCTTCAACCCGGGAGGTGGAGGTTGCAGTGAGCCCAG A C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs149285801 Functional Loss SNV dbSNP153 33..33 33 - - - 8150 RMVar_ID_8150 Human_SNP_ID_695612858 A-to-I Human chr21 + 41459716 41459716 41459716 CTACTCAGGAGGCTGAGACATGAGAATTGCTTAAACCCGGGAGGTGGAGGTTGCAGTGAGCCCAG CTACTCAGGAGGCTGAGACATGAGAATTGCTTTAACCCGGGAGGTGGAGGTTGCAGTGAGCCCAG A T - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs149285801 Functional Loss SNV dbSNP153 33..33 33 - - - 8151 RMVar_ID_8151 Human_SNP_ID_695620621 A-to-I Human chr21 - 41485527 41485527 41485527 CCCCAGCCTCAGCCCCCCAAGTGGCTGGGACTACAGGTGCTCGCCACCACACCTGGCTAATTTTT CCCCAGCCTCAGCCCCCCAAGTGGCTGGGACTGCAGGTGCTCGCCACCACACCTGGCTAATTTTT T C TMPRSS2 Ensembl:ENSG00000184012 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs912671149 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57752,RMVar_hsa_circ_58529 8152 RMVar_ID_8152 Human_SNP_ID_695621203 A-to-I Human chr21 - 41487917 41487917 41487917 GCGGTGGCGGGTGCCTGTAATTCCAGCTATTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCTG GCGGTGGCGGGTGCCTGTAATTCCAGCTATTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCTG T C TMPRSS2 Ensembl:ENSG00000184012 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1001409060 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57752,RMVar_hsa_circ_58529 8153 RMVar_ID_8153 Human_SNP_ID_695621214 A-to-I Human chr21 - 41487966 41487966 41487966 CAATATGGTGAAACCTTATCTCCACTAAAAATACAAAAATTAGCCAAGCGCGGTGGCGGGTGCCT CAATATGGTGAAACCTTATCTCCACTAAAAATGCAAAAATTAGCCAAGCGCGGTGGCGGGTGCCT T C TMPRSS2 Ensembl:ENSG00000184012 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs926484905 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57752,RMVar_hsa_circ_58529 8154 RMVar_ID_8154 Human_SNP_ID_695742980 A-to-I Human chr21 - 41927262 41927262 41927262 ACTTAGGAGGCTAAGGCAGGAGAATTGCTTAAACCCAGGAGGCGGAGGCTGCAGTGAGCCAAGAT ACTTAGGAGGCTAAGGCAGGAGAATTGCTTAAGCCCAGGAGGCGGAGGCTGCAGTGAGCCAAGAT T C C2CD2 Ensembl:ENSG00000157617 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs184492438 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39121,RMVar_hsa_circ_212406 8155 RMVar_ID_8155 Human_SNP_ID_695760148 A-to-I Human chr21 - 41992844 41992844 41992844 TCAGGTCCTTTAGTGCTTCTCAGTCAACAGACAGGGAGGGAGCTTCCCCTGTGACTGAGGTGCGC TCAGGTCCTTTAGTGCTTCTCAGTCAACAGACTGGGAGGGAGCTTCCCCTGTGACTGAGGTGCGC T A ZBTB21 Ensembl:ENSG00000173276 Protein coding CDS GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs779562322 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1604689,Human_RBP_ID_4673325,Human_RBP_ID_9299080,Human_RBP_ID_27490184 Human_miRNA_ID_2444658,Human_miRNA_ID_2444659 RMVar_hsa_circ_114414,RMVar_hsa_circ_109444,RMVar_hsa_circ_212412,RMVar_hsa_circ_212413 8156 RMVar_ID_8156 Human_SNP_ID_695955895 A-to-I Human chr21 + 42714224 42714224 42714224 TATTTTTAGTAGAGATGGGGTTTCACTGCATTAGCCAGGATGGTCTCGCTCTCCTGACCTCATGA TATTTTTAGTAGAGATGGGGTTTCACTGCATTCGCCAGGATGGTCTCGCTCTCCTGACCTCATGA A C PDE9A Ensembl:ENSG00000160191 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs987049573 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 8157 RMVar_ID_8157 Human_SNP_ID_695990115 A-to-I Human chr21 - 42838907 42838907 42838907 GTTCGAGATTCTCCTGCCTCAGCCTCCTGAATAGCTAGAATTACAGGTGTCCACCACGCCCGGCT GTTCGAGATTCTCCTGCCTCAGCCTCCTGAATGGCTAGAATTACAGGTGTCCACCACGCCCGGCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935579443 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23008363 8158 RMVar_ID_8158 Human_SNP_ID_695990132 A-to-I Human chr21 - 42838954 42838954 42838954 GGAGTGCAGTGGTGCAATCTTGGCTCACTGCAACCTCAGCCTCTCAGGTTCGAGATTCTCCTGCC GGAGTGCAGTGGTGCAATCTTGGCTCACTGCATCCTCAGCCTCTCAGGTTCGAGATTCTCCTGCC T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs543238951 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1937664 8159 RMVar_ID_8159 Human_SNP_ID_695990133 A-to-I Human chr21 - 42838954 42838954 42838954 GGAGTGCAGTGGTGCAATCTTGGCTCACTGCAACCTCAGCCTCTCAGGTTCGAGATTCTCCTGCC GGAGTGCAGTGGTGCAATCTTGGCTCACTGCAGCCTCAGCCTCTCAGGTTCGAGATTCTCCTGCC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs543238951 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1937664 8160 RMVar_ID_8160 Human_SNP_ID_695991896 A-to-I Human chr21 - 42843471 42843466 42843471 GGGAGTTTGAGGCTGCAGCAAGCCGTGATTGCACTACTGCATTCCAGCCTGGGTGACAGAGTGAC GGGAGTTTGAGGCTGCAGCAAGCCGTGATTGC_____TGCATTCCAGCCTGGGTGACAGAGTGAC AGTAGT A WDR4 Ensembl:ENSG00000160193 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1434030684 Functional Loss DEL dbSNP153 33..37 33 - - - Human_RBP_ID_207771,Human_RBP_ID_14317334,Human_RBP_ID_17572461,Human_RBP_ID_23928514,Human_RBP_ID_25645656 RMVar_hsa_circ_83292,RMVar_hsa_circ_87955,RMVar_hsa_circ_102409,RMVar_hsa_circ_86509,RMVar_hsa_circ_212430,RMVar_hsa_circ_212432,RMVar_hsa_circ_80464,RMVar_hsa_circ_212433,RMVar_hsa_circ_212431,RMVar_hsa_circ_212429 8161 RMVar_ID_8161 Human_SNP_ID_695991927 A-to-I Human chr21 - 42843559 42843559 42843559 AAAAAAAAAAAAAATTAGCCAGGTGTGGTGGCACATGCCTGTAGTCCCAGCTGCTCGGGAGGCTG AAAAAAAAAAAAAATTAGCCAGGTGTGGTGGCTCATGCCTGTAGTCCCAGCTGCTCGGGAGGCTG T A WDR4 Ensembl:ENSG00000160193 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049244609 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83292,RMVar_hsa_circ_87955,RMVar_hsa_circ_102409,RMVar_hsa_circ_86509,RMVar_hsa_circ_212430,RMVar_hsa_circ_212432,RMVar_hsa_circ_80464,RMVar_hsa_circ_212433,RMVar_hsa_circ_212431,RMVar_hsa_circ_212429 8162 RMVar_ID_8162 Human_SNP_ID_695991970 A-to-I Human chr21 - 42843690 42843690 42843690 ACATGCCTGTTGTCCCAGTTATTTGAGAGGCTAAAGCAGGAGAATCGCTTGAACCTGGGAGGCGG ACATGCCTGTTGTCCCAGTTATTTGAGAGGCTGAAGCAGGAGAATCGCTTGAACCTGGGAGGCGG T C WDR4 Ensembl:ENSG00000160193 Protein coding intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1159227943 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83292,RMVar_hsa_circ_87955,RMVar_hsa_circ_102409,RMVar_hsa_circ_86509,RMVar_hsa_circ_212430,RMVar_hsa_circ_212432,RMVar_hsa_circ_80464,RMVar_hsa_circ_212433,RMVar_hsa_circ_212431,RMVar_hsa_circ_212429 8163 RMVar_ID_8163 Human_SNP_ID_695991982 A-to-I Human chr21 - 42843749 42843749 42843749 CAGCTTGGCCAATATGGTGAAACCCTGTCTCTACTAAAAATATAAAAAATTAGCTGGGCACATGC CAGCTTGGCCAATATGGTGAAACCCTGTCTCTGCTAAAAATATAAAAAATTAGCTGGGCACATGC T C WDR4 Ensembl:ENSG00000160193 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1138783 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10038862,Human_RBP_ID_23010156,Human_RBP_ID_25645663 RMVar_hsa_circ_83292,RMVar_hsa_circ_87955,RMVar_hsa_circ_102409,RMVar_hsa_circ_86509,RMVar_hsa_circ_212430,RMVar_hsa_circ_212432,RMVar_hsa_circ_80464,RMVar_hsa_circ_212433,RMVar_hsa_circ_212431,RMVar_hsa_circ_212429 8164 RMVar_ID_8164 Human_SNP_ID_695991986 A-to-I Human chr21 - 42843760 42843760 42843760 GAGTTTGAGACCAGCTTGGCCAATATGGTGAAACCCTGTCTCTACTAAAAATATAAAAAATTAGC GAGTTTGAGACCAGCTTGGCCAATATGGTGAAGCCCTGTCTCTACTAAAAATATAAAAAATTAGC T C WDR4 Ensembl:ENSG00000160193 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1138782 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83292,RMVar_hsa_circ_87955,RMVar_hsa_circ_102409,RMVar_hsa_circ_86509,RMVar_hsa_circ_212430,RMVar_hsa_circ_212432,RMVar_hsa_circ_80464,RMVar_hsa_circ_212433,RMVar_hsa_circ_212431,RMVar_hsa_circ_212429 8165 RMVar_ID_8165 Human_SNP_ID_695992008 A-to-I Human chr21 - 42843854 42843854 42843854 AGACCTCATCTTTAAAAATAATTAAAAAGGTCAGGTGCGGTGGCTCACGCCTGTAATCCCAGCAT AGACCTCATCTTTAAAAATAATTAAAAAGGTCGGGTGCGGTGGCTCACGCCTGTAATCCCAGCAT T C WDR4 Ensembl:ENSG00000160193 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs763107368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14317349 RMVar_hsa_circ_83292,RMVar_hsa_circ_87955,RMVar_hsa_circ_102409,RMVar_hsa_circ_86509,RMVar_hsa_circ_212430,RMVar_hsa_circ_212432,RMVar_hsa_circ_80464,RMVar_hsa_circ_212433,RMVar_hsa_circ_212431,RMVar_hsa_circ_212429 8166 RMVar_ID_8166 Human_SNP_ID_695992020 A-to-I Human chr21 - 42843918 42843900 42843919 GGGAAGTTGAGGCAGGGGGATTGCTTGAGCCCAGGAGTTTGAGACTAGCCTGGGCAATACAGTGA GGGAAGTTGAGGCAGGGGGATTGCTTGAGCC___________________TGGGCAATACAGTGA AGGCTAGTCTCAAACTCCTG A WDR4 Ensembl:ENSG00000160193 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1007707571 Functional Loss DEL dbSNP153 32..50 33 - - - Human_RBP_ID_2705104,Human_RBP_ID_14317358,Human_RBP_ID_22818643 RMVar_hsa_circ_83292,RMVar_hsa_circ_87955,RMVar_hsa_circ_102409,RMVar_hsa_circ_86509,RMVar_hsa_circ_212430,RMVar_hsa_circ_212432,RMVar_hsa_circ_80464,RMVar_hsa_circ_212433,RMVar_hsa_circ_212431,RMVar_hsa_circ_212429 8167 RMVar_ID_8167 Human_SNP_ID_695992022 A-to-I Human chr21 - 42843918 42843918 42843918 GGGAAGTTGAGGCAGGGGGATTGCTTGAGCCCAGGAGTTTGAGACTAGCCTGGGCAATACAGTGA GGGAAGTTGAGGCAGGGGGATTGCTTGAGCCCGGGAGTTTGAGACTAGCCTGGGCAATACAGTGA T C WDR4 Ensembl:ENSG00000160193 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1298078667 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2705104,Human_RBP_ID_14317358,Human_RBP_ID_22818643 RMVar_hsa_circ_83292,RMVar_hsa_circ_87955,RMVar_hsa_circ_102409,RMVar_hsa_circ_86509,RMVar_hsa_circ_212430,RMVar_hsa_circ_212432,RMVar_hsa_circ_80464,RMVar_hsa_circ_212433,RMVar_hsa_circ_212431,RMVar_hsa_circ_212429 8168 RMVar_ID_8168 Human_SNP_ID_695992026 A-to-I Human chr21 - 42843937 42843937 42843937 CCTGTGATCCCAACACTTTGGGAAGTTGAGGCAGGGGGATTGCTTGAGCCCAGGAGTTTGAGACT CCTGTGATCCCAACACTTTGGGAAGTTGAGGCGGGGGGATTGCTTGAGCCCAGGAGTTTGAGACT T C WDR4 Ensembl:ENSG00000160193 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs530475160 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_150947,Human_RBP_ID_14317358 RMVar_hsa_circ_83292,RMVar_hsa_circ_87955,RMVar_hsa_circ_102409,RMVar_hsa_circ_86509,RMVar_hsa_circ_212430,RMVar_hsa_circ_212432,RMVar_hsa_circ_80464,RMVar_hsa_circ_212433,RMVar_hsa_circ_212431,RMVar_hsa_circ_212429 8169 RMVar_ID_8169 Human_SNP_ID_695992027 A-to-I Human chr21 - 42843946 42843946 42843946 CGGCTCACACCTGTGATCCCAACACTTTGGGAAGTTGAGGCAGGGGGATTGCTTGAGCCCAGGAG CGGCTCACACCTGTGATCCCAACACTTTGGGAGGTTGAGGCAGGGGGATTGCTTGAGCCCAGGAG T C WDR4 Ensembl:ENSG00000160193 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs981335331 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2705105,Human_RBP_ID_14317358,Human_RBP_ID_23928515 RMVar_hsa_circ_83292,RMVar_hsa_circ_87955,RMVar_hsa_circ_102409,RMVar_hsa_circ_86509,RMVar_hsa_circ_212430,RMVar_hsa_circ_212432,RMVar_hsa_circ_80464,RMVar_hsa_circ_212433,RMVar_hsa_circ_212431,RMVar_hsa_circ_212429 8170 RMVar_ID_8170 Human_SNP_ID_695992030 A-to-I Human chr21 - 42843957 42843957 42843957 AGCTAGGCTGGCGGCTCACACCTGTGATCCCAACACTTTGGGAAGTTGAGGCAGGGGGATTGCTT AGCTAGGCTGGCGGCTCACACCTGTGATCCCAGCACTTTGGGAAGTTGAGGCAGGGGGATTGCTT T C WDR4 Ensembl:ENSG00000160193 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1253820250 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2705105,Human_RBP_ID_14317358,Human_RBP_ID_17144909,Human_RBP_ID_20704208,Human_RBP_ID_23238668,Human_RBP_ID_23928515 RMVar_hsa_circ_83292,RMVar_hsa_circ_87955,RMVar_hsa_circ_102409,RMVar_hsa_circ_86509,RMVar_hsa_circ_212430,RMVar_hsa_circ_212432,RMVar_hsa_circ_80464,RMVar_hsa_circ_212433,RMVar_hsa_circ_212431,RMVar_hsa_circ_212429 8171 RMVar_ID_8171 Human_SNP_ID_695992587 A-to-I Human chr21 - 42845941 42845941 42845941 TTTTGTAGAGATGGTGTCTTGCTCTGCTGCCCAGGCTGGTCTCGAACTTCTGGCCTCAAGCAGTC TTTTGTAGAGATGGTGTCTTGCTCTGCTGCCCGGGCTGGTCTCGAACTTCTGGCCTCAAGCAGTC T C WDR4 Ensembl:ENSG00000160193 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1351994795 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2705127,Human_RBP_ID_10038880,Human_RBP_ID_14317582,Human_RBP_ID_20704294,Human_RBP_ID_22818651,Human_RBP_ID_23928557,Human_RBP_ID_27027982 RMVar_hsa_circ_83292,RMVar_hsa_circ_87955,RMVar_hsa_circ_102409,RMVar_hsa_circ_86509,RMVar_hsa_circ_212430,RMVar_hsa_circ_212432,RMVar_hsa_circ_80464,RMVar_hsa_circ_212433,RMVar_hsa_circ_212431,RMVar_hsa_circ_212429 8172 RMVar_ID_8172 Human_SNP_ID_695992902 A-to-I Human chr21 - 42846958 42846958 42846958 TCTCGGCTCACTGCAACCTCCACCTCACTGCAACCTCCGCCTCCCGGGTTCAAGCGATTCTCCTA TCTCGGCTCACTGCAACCTCCACCTCACTGCAGCCTCCGCCTCCCGGGTTCAAGCGATTCTCCTA T C WDR4 Ensembl:ENSG00000160193 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1235285471 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14317673,Human_RBP_ID_18516253 RMVar_hsa_circ_83292,RMVar_hsa_circ_87955,RMVar_hsa_circ_102409,RMVar_hsa_circ_86509,RMVar_hsa_circ_212430,RMVar_hsa_circ_212432,RMVar_hsa_circ_80464,RMVar_hsa_circ_212433,RMVar_hsa_circ_212431,RMVar_hsa_circ_212429 8173 RMVar_ID_8173 Human_SNP_ID_695992915 A-to-I Human chr21 - 42846991 42846991 42846991 CTCTGTTGCCCAGGCTGGAGTGCGGTGGCACAATCTCGGCTCACTGCAACCTCCACCTCACTGCA CTCTGTTGCCCAGGCTGGAGTGCGGTGGCACAGTCTCGGCTCACTGCAACCTCCACCTCACTGCA T C WDR4 Ensembl:ENSG00000160193 Protein coding intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1376378092 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23928579 RMVar_hsa_circ_83292,RMVar_hsa_circ_87955,RMVar_hsa_circ_102409,RMVar_hsa_circ_86509,RMVar_hsa_circ_212430,RMVar_hsa_circ_212432,RMVar_hsa_circ_80464,RMVar_hsa_circ_212433,RMVar_hsa_circ_212431,RMVar_hsa_circ_212429 8174 RMVar_ID_8174 Human_SNP_ID_696001437 A-to-I Human chr21 - 42872511 42872511 42872511 CGCCTCCCAGTTTCAAGCAATTCTCCCATCTCAGCCTCTCGAGTAGCTGGGACTATAGGTGCACA CGCCTCCCAGTTTCAAGCAATTCTCCCATCTCGGCCTCTCGAGTAGCTGGGACTATAGGTGCACA T C WDR4 Ensembl:ENSG00000160193 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1037698658 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18781634 RMVar_hsa_circ_102409,RMVar_hsa_circ_212433,RMVar_hsa_circ_289180,RMVar_hsa_circ_315645,RMVar_hsa_circ_212438,RMVar_hsa_circ_290281,RMVar_hsa_circ_212439,RMVar_hsa_circ_283309,RMVar_hsa_circ_212442,RMVar_hsa_circ_212444,RMVar_hsa_circ_296263,RMVar_hsa_circ_330889 8175 RMVar_ID_8175 Human_SNP_ID_696003185 A-to-I Human chr21 - 42877889 42877889 42877889 AGGCGCCTGCCACCATGCCTGGCTAATTTTTTATATTTTTAGTGGAGATGGGGGTTTCACTGTGT AGGCGCCTGCCACCATGCCTGGCTAATTTTTTTTATTTTTAGTGGAGATGGGGGTTTCACTGTGT T A WDR4 Ensembl:ENSG00000160193 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs959597277 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_150950 RMVar_hsa_circ_102409,RMVar_hsa_circ_212433 8176 RMVar_ID_8176 Human_SNP_ID_696003186 A-to-I Human chr21 - 42877889 42877889 42877889 AGGCGCCTGCCACCATGCCTGGCTAATTTTTTATATTTTTAGTGGAGATGGGGGTTTCACTGTGT AGGCGCCTGCCACCATGCCTGGCTAATTTTTTGTATTTTTAGTGGAGATGGGGGTTTCACTGTGT T C WDR4 Ensembl:ENSG00000160193 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs959597277 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_150950 RMVar_hsa_circ_102409,RMVar_hsa_circ_212433 8177 RMVar_ID_8177 Human_SNP_ID_696003955 A-to-I Human chr21 + 42880038 42880035 42880038 TGTAGCCCCAACTACTTGGGAGGCTGAGACAGAAGAATTGCCTGAACCCGGGAGGCGGAGGTTGC TGTAGCCCCAACTACTTGGGAGGCTGAGAC___AGAATTGCCTGAACCCGGGAGGCGGAGGTTGC CAGA C NDUFV3 Ensembl:ENSG00000160194 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1376806512 Functional Loss DEL dbSNP153 31..33 33 - - - 8178 RMVar_ID_8178 Human_SNP_ID_696003956 A-to-I Human chr21 + 42880038 42880038 42880038 TGTAGCCCCAACTACTTGGGAGGCTGAGACAGAAGAATTGCCTGAACCCGGGAGGCGGAGGTTGC TGTAGCCCCAACTACTTGGGAGGCTGAGACAGGAGAATTGCCTGAACCCGGGAGGCGGAGGTTGC A G NDUFV3 Ensembl:ENSG00000160194 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1337541881 Functional Loss SNV dbSNP153 33..33 33 - - - 8179 RMVar_ID_8179 Human_SNP_ID_696008228 A-to-I Human chr21 + 42894614 42894614 42894614 TCACTCTGTTGCCCAGGCCCAGGCTGGAGTGCAATGGCACCATCTCAACTCCCTGCAACTTCTGC TCACTCTGTTGCCCAGGCCCAGGCTGGAGTGCCATGGCACCATCTCAACTCCCTGCAACTTCTGC A C NDUFV3 Ensembl:ENSG00000160194 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs943528348 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109398,RMVar_hsa_circ_212448 8180 RMVar_ID_8180 Human_SNP_ID_696009430 A-to-I Human chr21 + 42898352 42898352 42898352 TCTCCCAGGCTGGAGTGCAGTGGCACAGTCATAGCTCACTACAGCCTCAAACTCCTGAGCTCAAG TCTCCCAGGCTGGAGTGCAGTGGCACAGTCATTGCTCACTACAGCCTCAAACTCCTGAGCTCAAG A T NDUFV3 Ensembl:ENSG00000160194 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1375323916 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109398,RMVar_hsa_circ_212449,RMVar_hsa_circ_99055,RMVar_hsa_circ_212448,RMVar_hsa_circ_313970,RMVar_hsa_circ_212450 8181 RMVar_ID_8181 Human_SNP_ID_696009436 A-to-I Human chr21 + 42898382 42898382 42898382 ATAGCTCACTACAGCCTCAAACTCCTGAGCTCAAGCAATCCTCCCACCTCAGCCTCCTGAGTAGC ATAGCTCACTACAGCCTCAAACTCCTGAGCTCGAGCAATCCTCCCACCTCAGCCTCCTGAGTAGC A G NDUFV3 Ensembl:ENSG00000160194 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054715533 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109398,RMVar_hsa_circ_212449,RMVar_hsa_circ_99055,RMVar_hsa_circ_212448,RMVar_hsa_circ_313970,RMVar_hsa_circ_212450 8182 RMVar_ID_8182 Human_SNP_ID_696009472 A-to-I Human chr21 + 42898569 42898569 42898569 ATAGGTCACTGCAGCCTCGACCTTCCAAGCTCAAGTGATCCTCCCACCTCAGCCCCTGGAGTAGC ATAGGTCACTGCAGCCTCGACCTTCCAAGCTCTAGTGATCCTCCCACCTCAGCCCCTGGAGTAGC A T NDUFV3 Ensembl:ENSG00000160194 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs937063906 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109398,RMVar_hsa_circ_212449,RMVar_hsa_circ_99055,RMVar_hsa_circ_212448,RMVar_hsa_circ_313970,RMVar_hsa_circ_212450 8183 RMVar_ID_8183 Human_SNP_ID_696009478 A-to-I Human chr21 + 42898599 42898592 42898600 TCAAGTGATCCTCCCACCTCAGCCCCTGGAGTAGCCAGGACTACAGGTGCACACCATCACACCCT TCAAGTGATCCTCCCACCTCAGCCCC________CCAGGACTACAGGTGCACACCATCACACCCT CTGGAGTAG C NDUFV3 Ensembl:ENSG00000160194 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1424860783 Functional Loss DEL dbSNP153 27..34 33 - - - RMVar_hsa_circ_109398,RMVar_hsa_circ_212449,RMVar_hsa_circ_99055,RMVar_hsa_circ_212448,RMVar_hsa_circ_313970,RMVar_hsa_circ_212450 8184 RMVar_ID_8184 Human_SNP_ID_696009503 A-to-I Human chr21 + 42898705 42898705 42898705 ATTGCCTAGACTGGTCTTGAATTCCTGGGCTCAAGCAATCTCCCTGCCTCAAACTCCCATAGTAT ATTGCCTAGACTGGTCTTGAATTCCTGGGCTCGAGCAATCTCCCTGCCTCAAACTCCCATAGTAT A G NDUFV3 Ensembl:ENSG00000160194 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886936004 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17572532 RMVar_hsa_circ_109398,RMVar_hsa_circ_212449,RMVar_hsa_circ_99055,RMVar_hsa_circ_212448,RMVar_hsa_circ_313970,RMVar_hsa_circ_212450 8185 RMVar_ID_8185 Human_SNP_ID_696009514 A-to-I Human chr21 + 42898745 42898745 42898745 TCCCTGCCTCAAACTCCCATAGTATTGGGATTACAGGTGTGAGCCACTGTGTCCAGCCTACCTGG TCCCTGCCTCAAACTCCCATAGTATTGGGATTGCAGGTGTGAGCCACTGTGTCCAGCCTACCTGG A G NDUFV3 Ensembl:ENSG00000160194 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1019488476 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3663452,Human_RBP_ID_14319720 RMVar_hsa_circ_109398,RMVar_hsa_circ_212449,RMVar_hsa_circ_99055,RMVar_hsa_circ_212448,RMVar_hsa_circ_313970,RMVar_hsa_circ_212450 8186 RMVar_ID_8186 Human_SNP_ID_696009771 A-to-I Human chr21 + 42899574 42899574 42899574 TCAAGCCATTCTCCTGCCCCATCCTCCCGAATAGCTGGGACTACAGGTGCCCGCCACCAAACCCG TCAAGCCATTCTCCTGCCCCATCCTCCCGAATGGCTGGGACTACAGGTGCCCGCCACCAAACCCG A G NDUFV3 Ensembl:ENSG00000160194 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs541699070 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109398,RMVar_hsa_circ_212449,RMVar_hsa_circ_99055,RMVar_hsa_circ_212448,RMVar_hsa_circ_313970,RMVar_hsa_circ_212450 8187 RMVar_ID_8187 Human_SNP_ID_696009880 A-to-I Human chr21 + 42899988 42899988 42899988 GGGAAGCTGAGGCGGGAGGATCAGTTGAGTTCAGCAGTTTGAGACAAGCCTGAGCAACATAGTGA GGGAAGCTGAGGCGGGAGGATCAGTTGAGTTCCGCAGTTTGAGACAAGCCTGAGCAACATAGTGA A C NDUFV3 Ensembl:ENSG00000160194 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1349192663 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14319763,Human_RBP_ID_17572566,Human_RBP_ID_22479546 RMVar_hsa_circ_109398,RMVar_hsa_circ_212449,RMVar_hsa_circ_99055,RMVar_hsa_circ_212448,RMVar_hsa_circ_313970,RMVar_hsa_circ_212450 8188 RMVar_ID_8188 Human_SNP_ID_696009971 A-to-I Human chr21 + 42900396 42900396 42900396 ATGGTGGCGGACGCCTGTAATCCCAGTCGCTCAGGAGGCTGAGGCAGGAGAATCGCTTGGACCCA ATGGTGGCGGACGCCTGTAATCCCAGTCGCTCGGGAGGCTGAGGCAGGAGAATCGCTTGGACCCA A G NDUFV3 Ensembl:ENSG00000160194 Protein coding intron GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs1455901990 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109398,RMVar_hsa_circ_212449,RMVar_hsa_circ_99055,RMVar_hsa_circ_212448,RMVar_hsa_circ_313970,RMVar_hsa_circ_212450 8189 RMVar_ID_8189 Human_SNP_ID_696009980 A-to-I Human chr21 + 42900435 42900435 42900435 TGAGGCAGGAGAATCGCTTGGACCCAGGAGGCAGAGGTTGCAATGAGCTGAGATTGTGCCATTGC TGAGGCAGGAGAATCGCTTGGACCCAGGAGGCGGAGGTTGCAATGAGCTGAGATTGTGCCATTGC A G NDUFV3 Ensembl:ENSG00000160194 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs960672117 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109398,RMVar_hsa_circ_212449,RMVar_hsa_circ_99055,RMVar_hsa_circ_212448,RMVar_hsa_circ_313970,RMVar_hsa_circ_212450 8190 RMVar_ID_8190 Human_SNP_ID_696009981 A-to-I Human chr21 + 42900444 42900444 42900444 AGAATCGCTTGGACCCAGGAGGCAGAGGTTGCAATGAGCTGAGATTGTGCCATTGCACTGCTTCT AGAATCGCTTGGACCCAGGAGGCAGAGGTTGCGATGAGCTGAGATTGTGCCATTGCACTGCTTCT A G NDUFV3 Ensembl:ENSG00000160194 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1301655973 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109398,RMVar_hsa_circ_212449,RMVar_hsa_circ_99055,RMVar_hsa_circ_212448,RMVar_hsa_circ_313970,RMVar_hsa_circ_212450 8191 RMVar_ID_8191 Human_SNP_ID_696012101 A-to-I Human chr21 + 42907719 42907719 42907719 GCAATCTGCCCGCCTCAGCCTCTCAAAGTGCTAGGATTACAGGTGTGAGCCACTGCTACTGGCCC GCAATCTGCCCGCCTCAGCCTCTCAAAGTGCTTGGATTACAGGTGTGAGCCACTGCTACTGGCCC A T NDUFV3 Ensembl:ENSG00000160194 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs528783945 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23185495 RMVar_hsa_circ_99055,RMVar_hsa_circ_212450 8192 RMVar_ID_8192 Human_SNP_ID_696012110 A-to-I Human chr21 + 42907776 42907775 42907776 ACTGGCCCCTGCTAATTTTTTATTCTTTGTAGAGACAGAGTCTCACTATTTTGCCCAGAATGATC ACTGGCCCCTGCTAATTTTTTATTCTTTGTAG_GACAGAGTCTCACTATTTTGCCCAGAATGATC GA G NDUFV3 Ensembl:ENSG00000160194 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1286672268 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_14320082 RMVar_hsa_circ_99055,RMVar_hsa_circ_212450 8193 RMVar_ID_8193 Human_SNP_ID_696012550 A-to-I Human chr21 + 42909303 42909303 42909303 AGGTGGGATTACAGGTACTCACCACCAGGTCCAGCTAACTTTTGTATTTTTAGTAGAGACAGGGT AGGTGGGATTACAGGTACTCACCACCAGGTCCGGCTAACTTTTGTATTTTTAGTAGAGACAGGGT A G NDUFV3 Ensembl:ENSG00000160194 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1375821518 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99055,RMVar_hsa_circ_212450 8194 RMVar_ID_8194 Human_SNP_ID_696012556 A-to-I Human chr21 + 42909331 42909331 42909331 GTCCAGCTAACTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTCGA GTCCAGCTAACTTTTGTATTTTTAGTAGAGACCGGGTTTCACCATGTTGGCCAGGCTGGTCTCGA A C NDUFV3 Ensembl:ENSG00000160194 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs891809534 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99055,RMVar_hsa_circ_212450 8195 RMVar_ID_8195 Human_SNP_ID_696012558 A-to-I Human chr21 + 42909342 42909342 42909342 TTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCT TTTTGTATTTTTAGTAGAGACAGGGTTTCACCGTGTTGGCCAGGCTGGTCTCGAACTCCTGACCT A G NDUFV3 Ensembl:ENSG00000160194 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs779379201 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99055,RMVar_hsa_circ_212450 8196 RMVar_ID_8196 Human_SNP_ID_696012565 A-to-I Human chr21 + 42909376 42909376 42909376 GTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAGATGGTCTGCCCACCTCCGCCTCCCAAAGTGC GTTGGCCAGGCTGGTCTCGAACTCCTGACCTCGGATGGTCTGCCCACCTCCGCCTCCCAAAGTGC A G NDUFV3 Ensembl:ENSG00000160194 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1202474298 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99055,RMVar_hsa_circ_212450 8197 RMVar_ID_8197 Human_SNP_ID_696012674 A-to-I Human chr21 + 42909820 42909820 42909820 TCCTGCCTTACTTAGCCTCTTGAGTAGCTGGTACTACAGGCTCACGCCACCATGCCTGGCTAATT TCCTGCCTTACTTAGCCTCTTGAGTAGCTGGTGCTACAGGCTCACGCCACCATGCCTGGCTAATT A G NDUFV3 Ensembl:ENSG00000160194 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs894942036 Functional Loss SNV dbSNP153 33..33 33 - - - 8198 RMVar_ID_8198 Human_SNP_ID_696012676 A-to-I Human chr21 + 42909823 42909822 42909823 TGCCTTACTTAGCCTCTTGAGTAGCTGGTACTACAGGCTCACGCCACCATGCCTGGCTAATTTTT TGCCTTACTTAGCCTCTTGAGTAGCTGGTACT_CAGGCTCACGCCACCATGCCTGGCTAATTTTT TA T NDUFV3 Ensembl:ENSG00000160194 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170916418 Functional Loss DEL dbSNP153 33..33 33 - - - 8199 RMVar_ID_8199 Human_SNP_ID_696012727 A-to-I Human chr21 + 42910076 42910076 42910076 GGCCAGGTGCAGTGGATAATTCCTGTAATCCCAGCGCTTTGGGAGGGCGAGGCGGGTGGAGCACC GGCCAGGTGCAGTGGATAATTCCTGTAATCCCTGCGCTTTGGGAGGGCGAGGCGGGTGGAGCACC A T NDUFV3 Ensembl:ENSG00000160194 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs571038454 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22723780 8200 RMVar_ID_8200 Human_SNP_ID_696012754 A-to-I Human chr21 + 42910143 42910143 42910143 AGGTCAGGAGTTGAGACCGGCCTGGCCAACATAGTGAAACCCCATCTCTACTAAAAATACAAAAA AGGTCAGGAGTTGAGACCGGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAA A G NDUFV3 Ensembl:ENSG00000160194 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs13046098 Functional Loss SNV dbSNP153 33..33 33 - - - 8201 RMVar_ID_8201 Human_SNP_ID_696013001 A-to-I Human chr21 - 42910950 42910950 42910950 GCGTAAGCCACCGTGCCCTGGCCCTCACCTACATTGGTTACTTTCTCTAAGTCAGACTGGGGGTC GCGTAAGCCACCGTGCCCTGGCCCTCACCTACGTTGGTTACTTTCTCTAAGTCAGACTGGGGGTC T C ERVH48-1 RNACentral:URS0000D5A870 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs915657357 Functional Loss SNV dbSNP153 33..33 33 - - - 8202 RMVar_ID_8202 Human_SNP_ID_696013185 A-to-I Human chr21 + 42911535 42911535 42911535 GCGATCTCAGCTCACTGCAGCCTCGTCCTCCCAGGCCCAAGCAATCCTCCCATCTCAGCCCACTT GCGATCTCAGCTCACTGCAGCCTCGTCCTCCCGGGCCCAAGCAATCCTCCCATCTCAGCCCACTT A G NDUFV3 Ensembl:ENSG00000160194 Protein coding 3'UTR GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1485758782 Functional Loss SNV dbSNP153 33..33 33 - - - 8203 RMVar_ID_8203 Human_SNP_ID_696013201 A-to-I Human chr21 + 42911594 42911594 42911594 CCACTTTGTAGCTGGGACTGTAGGCACTGGCCACCATGTCCGCCTAATTTTTCTATTTTTTGTAG CCACTTTGTAGCTGGGACTGTAGGCACTGGCCGCCATGTCCGCCTAATTTTTCTATTTTTTGTAG A G NDUFV3 Ensembl:ENSG00000160194 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432411281 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14320217 8204 RMVar_ID_8204 Human_SNP_ID_696013205 A-to-I Human chr21 + 42911607 42911607 42911607 GGGACTGTAGGCACTGGCCACCATGTCCGCCTAATTTTTCTATTTTTTGTAGAGACAGGGTTCAA GGGACTGTAGGCACTGGCCACCATGTCCGCCTGATTTTTCTATTTTTTGTAGAGACAGGGTTCAA A G NDUFV3 Ensembl:ENSG00000160194 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1429724171 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14320224 8205 RMVar_ID_8205 Human_SNP_ID_696013352 A-to-I Human chr21 + 42912149 42912149 42912149 GTAATCCCAGCTACTCAAGAGGCTGAGGCAGGAAAATCACTTGAACCCAGGAGGCAGAGGCTGCA GTAATCCCAGCTACTCAAGAGGCTGAGGCAGGGAAATCACTTGAACCCAGGAGGCAGAGGCTGCA A G NDUFV3 Ensembl:ENSG00000160194 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1356464204 Functional Loss SNV dbSNP153 33..33 33 - - - 8206 RMVar_ID_8206 Human_SNP_ID_696013556 A-to-I Human chr21 + 42912879 42912879 42912879 GCCTCACTGCACTCCAGCCTGGGCGAAAGAGCAAGACTCCGTCTCAAAAAAAAAAAACAAAAAAA GCCTCACTGCACTCCAGCCTGGGCGAAAGAGCGAGACTCCGTCTCAAAAAAAAAAAACAAAAAAA A G NDUFV3 Ensembl:ENSG00000160194 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs147244702 Functional Loss SNV dbSNP153 33..33 33 - - - 8207 RMVar_ID_8207 Human_SNP_ID_696014429 A-to-I Human chr21 + 42915936 42915936 42915936 TAAAAAATTTTTTGTAGAGATGGGGTTTCACCATGTTACCCAGGCTGCTCTCGAACTCCTGGACT TAAAAAATTTTTTGTAGAGATGGGGTTTCACCGTGTTACCCAGGCTGCTCTCGAACTCCTGGACT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1370032458 Functional Loss SNV dbSNP153 33..33 33 - - - 8208 RMVar_ID_8208 Human_SNP_ID_696032138 A-to-I Human chr21 + 42978123 42978123 42978123 TGCCTCCTGGGTGCAAGCAATTCTCTTGCCTCAACCTCCCGAGTAGCTGGGATAACAGGTGTGCA TGCCTCCTGGGTGCAAGCAATTCTCTTGCCTCCACCTCCCGAGTAGCTGGGATAACAGGTGTGCA A C PKNOX1 Ensembl:ENSG00000160199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs757472406 Functional Loss SNV dbSNP153 33..33 33 - - - 8209 RMVar_ID_8209 Human_SNP_ID_696032303 A-to-I Human chr21 + 42978623 42978623 42978623 CTCTTGCCTCAGCCTACCAAGTAGTTGGGACTACAGACGTGAGCCACCACGCCCGGCTAATTTTT CTCTTGCCTCAGCCTACCAAGTAGTTGGGACTGCAGACGTGAGCCACCACGCCCGGCTAATTTTT A G PKNOX1 Ensembl:ENSG00000160199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1485014413 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14321052 8210 RMVar_ID_8210 Human_SNP_ID_696032313 A-to-I Human chr21 + 42978658 42978658 42978658 GACGTGAGCCACCACGCCCGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCGCCGTATTGG GACGTGAGCCACCACGCCCGGCTAATTTTTGTGTTTTTAGTAGAGACAGGGTTTCGCCGTATTGG A G PKNOX1 Ensembl:ENSG00000160199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs774098491 Functional Loss SNV dbSNP153 33..33 33 - - - 8211 RMVar_ID_8211 Human_SNP_ID_696032327 A-to-I Human chr21 + 42978686 42978686 42978686 TTGTATTTTTAGTAGAGACAGGGTTTCGCCGTATTGGCCAGGCTGGTCTTGAACTCCTGACCTCA TTGTATTTTTAGTAGAGACAGGGTTTCGCCGTGTTGGCCAGGCTGGTCTTGAACTCCTGACCTCA A G PKNOX1 Ensembl:ENSG00000160199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285582647 Functional Loss SNV dbSNP153 33..33 33 - - - 8212 RMVar_ID_8212 Human_SNP_ID_696032565 A-to-I Human chr21 + 42979605 42979605 42979605 TCTACTAAATATACAAAGAATTAGCTGGGCGTAGTGGCGGGCACCTGTATTCTCAGCCACTTGGG TCTACTAAATATACAAAGAATTAGCTGGGCGTGGTGGCGGGCACCTGTATTCTCAGCCACTTGGG A G PKNOX1 Ensembl:ENSG00000160199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474536020 Functional Loss SNV dbSNP153 33..33 33 - - - 8213 RMVar_ID_8213 Human_SNP_ID_696033081 A-to-I Human chr21 + 42981699 42981699 42981699 TTCCCGCCACAGCCCCCAAAGTAGCTGGGATTACAGGCACGTGTCATCACACCCAGCTAATTGTA TTCCCGCCACAGCCCCCAAAGTAGCTGGGATTGCAGGCACGTGTCATCACACCCAGCTAATTGTA A G PKNOX1 Ensembl:ENSG00000160199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1000911199 Functional Loss SNV dbSNP153 33..33 33 - - - 8214 RMVar_ID_8214 Human_SNP_ID_696034094 A-to-I Human chr21 + 42985177 42985177 42985177 GCCCGGCTAATTTTTGTACTTGCAGTAGAGACAGGTTTCACCACGTTGGCCAGGCTGATCTCGAA GCCCGGCTAATTTTTGTACTTGCAGTAGAGACGGGTTTCACCACGTTGGCCAGGCTGATCTCGAA A G PKNOX1 Ensembl:ENSG00000160199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs963891128 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14321422 8215 RMVar_ID_8215 Human_SNP_ID_696034172 A-to-I Human chr21 + 42985414 42985414 42985414 TGGAGTGCAGGGGAGTGATCTTGGCTCACTGCAGTCTCCACCTCCTGGGTTCAAGTGATTCTCTG TGGAGTGCAGGGGAGTGATCTTGGCTCACTGCGGTCTCCACCTCCTGGGTTCAAGTGATTCTCTG A G PKNOX1 Ensembl:ENSG00000160199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965167958 Functional Loss SNV dbSNP153 33..33 33 - - - 8216 RMVar_ID_8216 Human_SNP_ID_696034282 A-to-I Human chr21 + 42985878 42985878 42985878 AAAAAATTAGCTGGTCATGGTGGCGGGTGCCTATAATTCCAGCTACTCAGGAGACTGAGGCAGGA AAAAAATTAGCTGGTCATGGTGGCGGGTGCCTGTAATTCCAGCTACTCAGGAGACTGAGGCAGGA A G PKNOX1 Ensembl:ENSG00000160199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1347000574 Functional Loss SNV dbSNP153 33..33 33 - - - 8217 RMVar_ID_8217 Human_SNP_ID_696034632 A-to-I Human chr21 + 42987221 42987221 42987221 CTGACCAACATGGAGAAACTCTTGTCTCTACTAAAAATACAAAACTAGCTGGGCGTGGTGGCGCA CTGACCAACATGGAGAAACTCTTGTCTCTACTGAAAATACAAAACTAGCTGGGCGTGGTGGCGCA A G PKNOX1 Ensembl:ENSG00000160199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1254594709 Functional Loss SNV dbSNP153 33..33 33 - - - 8218 RMVar_ID_8218 Human_SNP_ID_696035467 A-to-I Human chr21 + 42989548 42989548 42989548 AAGTGATTCTCTCAAGTCTCAGCCTCCCGAGTAGCTGGGATTACAGGCGCCTGCTACCACGCCTG AAGTGATTCTCTCAAGTCTCAGCCTCCCGAGTGGCTGGGATTACAGGCGCCTGCTACCACGCCTG A G PKNOX1 Ensembl:ENSG00000160199 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1158989875 Functional Loss SNV dbSNP153 33..33 33 - - - 8219 RMVar_ID_8219 Human_SNP_ID_696035468 A-to-I Human chr21 + 42989555 42989555 42989555 TCTCTCAAGTCTCAGCCTCCCGAGTAGCTGGGATTACAGGCGCCTGCTACCACGCCTGGCTAATT TCTCTCAAGTCTCAGCCTCCCGAGTAGCTGGGTTTACAGGCGCCTGCTACCACGCCTGGCTAATT A T PKNOX1 Ensembl:ENSG00000160199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs990147260 Functional Loss SNV dbSNP153 33..33 33 - - - 8220 RMVar_ID_8220 Human_SNP_ID_696035542 A-to-I Human chr21 + 42989915 42989915 42989915 GAGCTCAGGAGTTTGAGGCTAGCCTGGGCAACATGGCAAAACCCTGTCTCTACAAAAAATACAAA GAGCTCAGGAGTTTGAGGCTAGCCTGGGCAACGTGGCAAAACCCTGTCTCTACAAAAAATACAAA A G PKNOX1 Ensembl:ENSG00000160199 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1460292738 Functional Loss SNV dbSNP153 33..33 33 - - - 8221 RMVar_ID_8221 Human_SNP_ID_696037178 A-to-I Human chr21 + 42995422 42995422 42995422 GTCTTGAGCCTGGTGCTGTGGCACATGCCTGTAATCCCAGCGCTTTGGGAGGCGGAGGTAGGAGG GTCTTGAGCCTGGTGCTGTGGCACATGCCTGTCATCCCAGCGCTTTGGGAGGCGGAGGTAGGAGG A C PKNOX1 Ensembl:ENSG00000160199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs562482708 Functional Loss SNV dbSNP153 33..33 33 - - - 8222 RMVar_ID_8222 Human_SNP_ID_696038720 A-to-I Human chr21 + 43001794 43001794 43001794 CGTCCTGGCTAACATGGTGAAACCCCGTCTCTACTGAAAAGACAAAAAATTAGCCGGACGTAGTC CGTCCTGGCTAACATGGTGAAACCCCGTCTCTGCTGAAAAGACAAAAAATTAGCCGGACGTAGTC A G PKNOX1 Ensembl:ENSG00000160199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs570887349 Functional Loss SNV dbSNP153 33..33 33 - - - 8223 RMVar_ID_8223 Human_SNP_ID_696051726 A-to-I Human chr21 - 43054405 43054405 43054405 AAGAACACTGGCTTGGCCAGGCACAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGCCGAGG AAGAACACTGGCTTGGCCAGGCACAGTGGCTCGCGCCTGTAATCCCAGCACTTTGGGAGCCGAGG T C CBS Ensembl:ENSG00000160200 Protein coding intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1029753946 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27028192 RMVar_hsa_circ_108104,RMVar_hsa_circ_120409,RMVar_hsa_circ_125645,RMVar_hsa_circ_123347,RMVar_hsa_circ_119851,RMVar_hsa_circ_212465,RMVar_hsa_circ_75860,RMVar_hsa_circ_107488,RMVar_hsa_circ_212467,RMVar_hsa_circ_212469,RMVar_hsa_circ_212470,RMVar_hsa_circ_212468,RMVar_hsa_circ_212466,RMVar_hsa_circ_212464 8224 RMVar_ID_8224 Human_SNP_ID_696051795 A-to-I Human chr21 - 43054798 43054798 43054798 TGCTCAACTGATCCTTCTGCCTCAGTCTCCCAAGTAGCTGGGACCACAAGCGTGTGCCACCATGC TGCTCAACTGATCCTTCTGCCTCAGTCTCCCAGGTAGCTGGGACCACAAGCGTGTGCCACCATGC T C CBS Ensembl:ENSG00000160200 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs933002001 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27028199 RMVar_hsa_circ_108104,RMVar_hsa_circ_120409,RMVar_hsa_circ_125645,RMVar_hsa_circ_123347,RMVar_hsa_circ_119851,RMVar_hsa_circ_212465,RMVar_hsa_circ_75860,RMVar_hsa_circ_107488,RMVar_hsa_circ_212467,RMVar_hsa_circ_212469,RMVar_hsa_circ_212470,RMVar_hsa_circ_212468,RMVar_hsa_circ_212466,RMVar_hsa_circ_212464 8225 RMVar_ID_8225 Human_SNP_ID_696051801 A-to-I Human chr21 - 43054855 43054855 43054855 TGTTGCCGACTGGAGTGCAGTAGTGCCATCATAGCTCGCTGCAGCCTCGACCTGCTGTGCTCAAC TGTTGCCGACTGGAGTGCAGTAGTGCCATCATGGCTCGCTGCAGCCTCGACCTGCTGTGCTCAAC T C CBS Ensembl:ENSG00000160200 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs11552089 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3663551,Human_RBP_ID_14323018,Human_RBP_ID_22082457,Human_RBP_ID_22263426,Human_RBP_ID_27028200,Human_RBP_ID_27301989 RMVar_hsa_circ_108104,RMVar_hsa_circ_120409,RMVar_hsa_circ_125645,RMVar_hsa_circ_123347,RMVar_hsa_circ_119851,RMVar_hsa_circ_212465,RMVar_hsa_circ_75860,RMVar_hsa_circ_107488,RMVar_hsa_circ_212467,RMVar_hsa_circ_212469,RMVar_hsa_circ_212470,RMVar_hsa_circ_212468,RMVar_hsa_circ_212466,RMVar_hsa_circ_212464 8226 RMVar_ID_8226 Human_SNP_ID_696064722 A-to-I Human chr21 - 43115557 43115557 43115557 TTGATCCTTGGAACGAAAGGATGGCCATGTTCAGAGTGTATGACAACATCAGGATCCTGGGAAAC TTGATCCTTGGAACGAAAGGATGGCCATGTTCTGAGTGTATGACAACATCAGGATCCTGGGAAAC T A MRPL51P2 Ensembl:ENSG00000232777 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569034712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1880835,Human_miRNA_ID_1880836,Human_miRNA_ID_1893082,Human_miRNA_ID_1893083 8227 RMVar_ID_8227 Human_SNP_ID_696130099 A-to-I Human chr21 + 43432965 43432965 43432965 GAGAGTCGGGAACCAAGGGCGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGA GAGAGTCGGGAACCAAGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1362934733 Functional Loss SNV dbSNP153 33..33 33 - - - 8228 RMVar_ID_8228 Human_SNP_ID_696176878 A-to-I Human chr21 + 43663289 43663288 43663290 CGTTTGTTTTGTGTGTTTTTGTTTTTTGAGACAGAGTTTCACTCTTTCACCCAGGCTGAAGTGCA CGTTTGTTTTGTGTGTTTTTGTTTTTTGAGAC__AGTTTCACTCTTTCACCCAGGCTGAAGTGCA CAG C RRP1B Ensembl:ENSG00000160208 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs973657491 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_95467,RMVar_hsa_circ_212491 8229 RMVar_ID_8229 Human_SNP_ID_696181273 A-to-I Human chr21 + 43680747 43680747 43680747 TTTATTTTTTGTAGAGACAGGGGTCTCACTATATTGCCCAGGCTGGTCTTAAACTGTTAGGCTTA TTTATTTTTTGTAGAGACAGGGGTCTCACTATGTTGCCCAGGCTGGTCTTAAACTGTTAGGCTTA A G RRP1B Ensembl:ENSG00000160208 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1481297130 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14326932 RMVar_hsa_circ_95467,RMVar_hsa_circ_109708,RMVar_hsa_circ_212491,RMVar_hsa_circ_77803,RMVar_hsa_circ_93856,RMVar_hsa_circ_212493,RMVar_hsa_circ_212494,RMVar_hsa_circ_61938,RMVar_hsa_circ_37216,RMVar_hsa_circ_110604,RMVar_hsa_circ_212495,RMVar_hsa_circ_212496,RMVar_hsa_circ_82271,RMVar_hsa_circ_212498,RMVar_hsa_circ_93348,RMVar_hsa_circ_212499 8230 RMVar_ID_8230 Human_SNP_ID_696181328 A-to-I Human chr21 + 43681011 43681011 43681011 CCTATAATCCCAGCACTCTGGGAAGCCCAGGCAGTCGGATAACTTGAGGTCAGGAGTTCGAGACC CCTATAATCCCAGCACTCTGGGAAGCCCAGGCCGTCGGATAACTTGAGGTCAGGAGTTCGAGACC A C RRP1B Ensembl:ENSG00000160208 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1207471988 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14326948 RMVar_hsa_circ_95467,RMVar_hsa_circ_109708,RMVar_hsa_circ_212491,RMVar_hsa_circ_77803,RMVar_hsa_circ_93856,RMVar_hsa_circ_212493,RMVar_hsa_circ_212494,RMVar_hsa_circ_61938,RMVar_hsa_circ_37216,RMVar_hsa_circ_110604,RMVar_hsa_circ_212495,RMVar_hsa_circ_212496,RMVar_hsa_circ_82271,RMVar_hsa_circ_212498,RMVar_hsa_circ_93348,RMVar_hsa_circ_212499 8231 RMVar_ID_8231 Human_SNP_ID_696181355 A-to-I Human chr21 + 43681118 43681118 43681118 CAAAAATTAGCCAGGTATGGTGGCGGTCGCCTATAGTCCCAGCTACTTGGGAGGCTGAGGTGGGA CAAAAATTAGCCAGGTATGGTGGCGGTCGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGTGGGA A G RRP1B Ensembl:ENSG00000160208 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs979691471 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25646865 RMVar_hsa_circ_95467,RMVar_hsa_circ_109708,RMVar_hsa_circ_212491,RMVar_hsa_circ_77803,RMVar_hsa_circ_93856,RMVar_hsa_circ_212493,RMVar_hsa_circ_212494,RMVar_hsa_circ_61938,RMVar_hsa_circ_37216,RMVar_hsa_circ_110604,RMVar_hsa_circ_212495,RMVar_hsa_circ_212496,RMVar_hsa_circ_82271,RMVar_hsa_circ_212498,RMVar_hsa_circ_93348,RMVar_hsa_circ_212499 8232 RMVar_ID_8232 Human_SNP_ID_696192257 A-to-I Human chr21 + 43720935 43720935 43720935 TTCCTTCTTTGGCTCACTCGGGATCCCCCAGCAATGTCCTTTGTTCTCGAACTCCCAGTGACTCG TTCCTTCTTTGGCTCACTCGGGATCCCCCAGCGATGTCCTTTGTTCTCGAACTCCCAGTGACTCG A G PDXK Ensembl:ENSG00000160209 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1164710161 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2705694,Human_RBP_ID_3666386 8233 RMVar_ID_8233 Human_SNP_ID_696193183 A-to-I Human chr21 + 43724720 43724720 43724720 AAAAAAAAGCTGGCTATGTGACTCACATCTGTAGTCCCACCTACTTGGGAAGGTGAAGTGGGAGG AAAAAAAAGCTGGCTATGTGACTCACATCTGTGGTCCCACCTACTTGGGAAGGTGAAGTGGGAGG A G PDXK Ensembl:ENSG00000160209 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1213820501 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2705703 8234 RMVar_ID_8234 Human_SNP_ID_696193184 A-to-I Human chr21 + 43724720 43724720 43724720 AAAAAAAAGCTGGCTATGTGACTCACATCTGTAGTCCCACCTACTTGGGAAGGTGAAGTGGGAGG AAAAAAAAGCTGGCTATGTGACTCACATCTGTTGTCCCACCTACTTGGGAAGGTGAAGTGGGAGG A T PDXK Ensembl:ENSG00000160209 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1213820501 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2705703 8235 RMVar_ID_8235 Human_SNP_ID_696193358 A-to-I Human chr21 + 43725305 43725304 43725306 AGATCGCGCCACTGCACTCCAGCACGGGCGACAGAGCAAGACTCTCGTCTCAAAACAAAACAAAA AGATCGCGCCACTGCACTCCAGCACGGGCGAC__AGCAAGACTCTCGTCTCAAAACAAAACAAAA CAG C PDXK Ensembl:ENSG00000160209 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1405314613 Functional Loss DEL dbSNP153 33..34 33 - - - 8236 RMVar_ID_8236 Human_SNP_ID_696194803 A-to-I Human chr21 + 43730154 43730154 43730154 TTGATTGATTTGGTTTGATTTGAATTTTTTTGAGGCAGAGTCTCTCTCTGTCACCCAGGCTAGTT TTGATTGATTTGGTTTGATTTGAATTTTTTTGGGGCAGAGTCTCTCTCTGTCACCCAGGCTAGTT A G PDXK Ensembl:ENSG00000160209 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1366796617 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2705711,Human_RBP_ID_14328089 8237 RMVar_ID_8237 Human_SNP_ID_696194934 A-to-I Human chr21 + 43730698 43730698 43730698 TATGTAGTCTGGGTGCAGTGGCTCATACCTGTAGTCCCAGCACTTTGGGAGGCTAAGGGAGGAGA TATGTAGTCTGGGTGCAGTGGCTCATACCTGTGGTCCCAGCACTTTGGGAGGCTAAGGGAGGAGA A G PDXK Ensembl:ENSG00000160209 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs897300755 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2705712 8238 RMVar_ID_8238 Human_SNP_ID_696195015 A-to-I Human chr21 + 43731032 43731032 43731032 ATTTTTTTTTTAAATAGAGATGGAATCTTGCTATGTTGCTCAGTCTGGTCTTGAACTCCTGGGCT ATTTTTTTTTTAAATAGAGATGGAATCTTGCTGTGTTGCTCAGTCTGGTCTTGAACTCCTGGGCT A G PDXK Ensembl:ENSG00000160209 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1280543818 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4674669,Human_RBP_ID_17572465 8239 RMVar_ID_8239 Human_SNP_ID_696200515 A-to-I Human chr21 + 43747015 43747015 43747015 AGACAATGAGCTGGGTGTGGTGGCACCTACCTATAGTCCCAACTACTTGGGAGGCTGAGGTGGGA AGACAATGAGCTGGGTGTGGTGGCACCTACCTGTAGTCCCAACTACTTGGGAGGCTGAGGTGGGA A G PDXK Ensembl:ENSG00000160209 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs982990229 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90856,RMVar_hsa_circ_305228,RMVar_hsa_circ_315115,RMVar_hsa_circ_374028,RMVar_hsa_circ_212507,RMVar_hsa_circ_212505,RMVar_hsa_circ_212506,RMVar_hsa_circ_114250,RMVar_hsa_circ_77911,RMVar_hsa_circ_115153,RMVar_hsa_circ_212511,RMVar_hsa_circ_212512,RMVar_hsa_circ_212514,RMVar_hsa_circ_124794,RMVar_hsa_circ_273254,RMVar_hsa_circ_212516,RMVar_hsa_circ_212517,RMVar_hsa_circ_212515 8240 RMVar_ID_8240 Human_SNP_ID_696207226 A-to-I Human chr21 + 43769699 43769699 43769699 AAGGTGGCATGCATCTGTAGTTCCAGCTGCTCAGGAGGCTGAGGCAGGAGGATCACCTGAGCTAG AAGGTGGCATGCATCTGTAGTTCCAGCTGCTCTGGAGGCTGAGGCAGGAGGATCACCTGAGCTAG A T AP001053.1 Ensembl:ENSG00000287507 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1175837229 Functional Loss SNV dbSNP153 33..33 33 - - - 8241 RMVar_ID_8241 Human_SNP_ID_696241767 A-to-I Human chr21 + 43887794 43887794 43887794 CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTATAGGCGCCCGCCATCACACCCACTGACTTTTG CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTGTAGGCGCCCGCCATCACACCCACTGACTTTTG A G AGPAT3 Ensembl:ENSG00000160216 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1218240242 Functional Loss SNV dbSNP153 33..33 33 - - - 8242 RMVar_ID_8242 Human_SNP_ID_696241790 A-to-I Human chr21 + 43887874 43887874 43887874 CTGGGTTTCGCCATGTTGGCCAGGCTGGTCTCAAACTCCTGAGCTCAAGTGAACTCCTGCCTCAG CTGGGTTTCGCCATGTTGGCCAGGCTGGTCTCCAACTCCTGAGCTCAAGTGAACTCCTGCCTCAG A C AGPAT3 Ensembl:ENSG00000160216 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1477977801 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14332291 8243 RMVar_ID_8243 Human_SNP_ID_696262107 A-to-I Human chr21 + 43960976 43960973 43960976 CAGCCTGAGCAACATGGTGAAACCCTGTCTCTACTAAAAATACAAAATTAGCTGAGCATGGTGGT CAGCCTGAGCAACATGGTGAAACCCTGTCT___CTAAAAATACAAAATTAGCTGAGCATGGTGGT TCTA T AGPAT3 Ensembl:ENSG00000160216 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1192173463 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_23929856 RMVar_hsa_circ_121679,RMVar_hsa_circ_324953,RMVar_hsa_circ_212529,RMVar_hsa_circ_212530 8244 RMVar_ID_8244 Human_SNP_ID_696263311 A-to-I Human chr21 + 43965158 43965158 43965158 TGCCATGTTGCCCAGACTGGTCTCCAACTCCTAGGCTCATGTGATCCTCCTGCCTCAGCCTGCTG TGCCATGTTGCCCAGACTGGTCTCCAACTCCTGGGCTCATGTGATCCTCCTGCCTCAGCCTGCTG A G AGPAT3 Ensembl:ENSG00000160216 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1032484232 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121679,RMVar_hsa_circ_324953,RMVar_hsa_circ_212529,RMVar_hsa_circ_212530 8245 RMVar_ID_8245 Human_SNP_ID_696263433 A-to-I Human chr21 + 43965668 43965668 43965668 GAGTCTCTCTGTTGTCCTGGCTGGAGCACAGCAGTGCGATCTTGGCTCACTGCAACCTCCATCTT GAGTCTCTCTGTTGTCCTGGCTGGAGCACAGCGGTGCGATCTTGGCTCACTGCAACCTCCATCTT A G AGPAT3 Ensembl:ENSG00000160216 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1427811256 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14333640 RMVar_hsa_circ_121679,RMVar_hsa_circ_324953,RMVar_hsa_circ_212529,RMVar_hsa_circ_212530 8246 RMVar_ID_8246 Human_SNP_ID_696263450 A-to-I Human chr21 + 43965752 43965752 43965752 CGTGCCCCAGCCTCCCAAGTAGCTGGGATTACAGGTGCCTGCCACCACATCCAGCTAATTTTTTT CGTGCCCCAGCCTCCCAAGTAGCTGGGATTACGGGTGCCTGCCACCACATCCAGCTAATTTTTTT A G AGPAT3 Ensembl:ENSG00000160216 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1253394371 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121679,RMVar_hsa_circ_324953,RMVar_hsa_circ_212529,RMVar_hsa_circ_212530 8247 RMVar_ID_8247 Human_SNP_ID_696263477 A-to-I Human chr21 + 43965847 43965847 43965847 GCTTCCCCAGCTGGTCTTGAACTCCTGGCCTCAAGTGATCCTCCTGTCTCGGCCTCCCAAAGTGC GCTTCCCCAGCTGGTCTTGAACTCCTGGCCTCCAGTGATCCTCCTGTCTCGGCCTCCCAAAGTGC A C AGPAT3 Ensembl:ENSG00000160216 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs1410206516 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121679,RMVar_hsa_circ_324953,RMVar_hsa_circ_212529,RMVar_hsa_circ_212530 8248 RMVar_ID_8248 Human_SNP_ID_696284540 A-to-I Human chr21 + 44040868 44040868 44040868 AAACTCCTGGCCCCAAGTGATCCTCCTGCCTCAGTCCCCTGAAGTGCTGGGACTACAGGTGTGAG AAACTCCTGGCCCCAAGTGATCCTCCTGCCTCGGTCCCCTGAAGTGCTGGGACTACAGGTGTGAG A G TRAPPC10 Ensembl:ENSG00000160218 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1246886302 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_573382,Human_RBP_ID_14335011 RMVar_hsa_circ_20777,RMVar_hsa_circ_87707,RMVar_hsa_circ_212534,RMVar_hsa_circ_59795,RMVar_hsa_circ_345151,RMVar_hsa_circ_347561,RMVar_hsa_circ_60251,RMVar_hsa_circ_301612,RMVar_hsa_circ_338165,RMVar_hsa_circ_212535,RMVar_hsa_circ_328993,RMVar_hsa_circ_64013,RMVar_hsa_circ_212536,RMVar_hsa_circ_212537 8249 RMVar_ID_8249 Human_SNP_ID_696284785 A-to-I Human chr21 + 44041826 44041826 44041826 TCGACTCACTGCAACCTCTGCCTCCCAGGTCCAAGTGATTCTTCTGCCTCAGACTCCCAGTAGCT TCGACTCACTGCAACCTCTGCCTCCCAGGTCCGAGTGATTCTTCTGCCTCAGACTCCCAGTAGCT A G TRAPPC10 Ensembl:ENSG00000160218 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1272276131 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14335059 RMVar_hsa_circ_20777,RMVar_hsa_circ_87707,RMVar_hsa_circ_212534,RMVar_hsa_circ_59795,RMVar_hsa_circ_345151,RMVar_hsa_circ_347561,RMVar_hsa_circ_60251,RMVar_hsa_circ_301612,RMVar_hsa_circ_338165,RMVar_hsa_circ_212535,RMVar_hsa_circ_328993,RMVar_hsa_circ_64013,RMVar_hsa_circ_212536,RMVar_hsa_circ_212537 8250 RMVar_ID_8250 Human_SNP_ID_696286206 A-to-I Human chr21 - 44047011 44047011 44047011 AAATGGCTGGCAGTAAGGTGGGAAAGGACTCCAGAAAGGCCAAGACAAAGGCGGTTTCCCGCTCG AAATGGCTGGCAGTAAGGTGGGAAAGGACTCCGGAAAGGCCAAGACAAAGGCGGTTTCCCGCTCG T C H2AZP1 Ensembl:ENSG00000213440 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1239152346 Functional Loss SNV dbSNP153 33..33 33 - - - 8251 RMVar_ID_8251 Human_SNP_ID_696286218 A-to-I Human chr21 - 44047032 44047032 44047032 CTTGAGCTTCAGCAGAATTCGAAATGGCTGGCAGTAAGGTGGGAAAGGACTCCAGAAAGGCCAAG CTTGAGCTTCAGCAGAATTCGAAATGGCTGGCGGTAAGGTGGGAAAGGACTCCAGAAAGGCCAAG T C H2AZP1 Ensembl:ENSG00000213440 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1314668642 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4682707,Human_RBP_ID_27028961 8252 RMVar_ID_8252 Human_SNP_ID_696287356 A-to-I Human chr21 + 44051172 44051172 44051172 GCAATCCACCCACCTTAGCCTCCCAAAGTGCTAGGATTACAGGTGTGAGCCACTGTGCCTGGCCA GCAATCCACCCACCTTAGCCTCCCAAAGTGCTCGGATTACAGGTGTGAGCCACTGTGCCTGGCCA A C TRAPPC10 Ensembl:ENSG00000160218 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1367245061 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20777,RMVar_hsa_circ_87707,RMVar_hsa_circ_212534,RMVar_hsa_circ_59795,RMVar_hsa_circ_345151,RMVar_hsa_circ_347561,RMVar_hsa_circ_60251,RMVar_hsa_circ_301612,RMVar_hsa_circ_338165,RMVar_hsa_circ_212535,RMVar_hsa_circ_328993,RMVar_hsa_circ_64013,RMVar_hsa_circ_212536,RMVar_hsa_circ_212537 8253 RMVar_ID_8253 Human_SNP_ID_696291879 A-to-I Human chr21 + 44068009 44068009 44068009 GGGCGTGATGGCAGGCGCCTGTAATCCCAGCTACTCGGGAGGCTGGGGCGGGAGAATTGCTTGAA GGGCGTGATGGCAGGCGCCTGTAATCCCAGCTGCTCGGGAGGCTGGGGCGGGAGAATTGCTTGAA A G TRAPPC10 Ensembl:ENSG00000160218 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1301315572 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_212538,RMVar_hsa_circ_87707,RMVar_hsa_circ_212534,RMVar_hsa_circ_60251,RMVar_hsa_circ_64013,RMVar_hsa_circ_316196,RMVar_hsa_circ_356808,RMVar_hsa_circ_362162,RMVar_hsa_circ_374841,RMVar_hsa_circ_309804,RMVar_hsa_circ_212540,RMVar_hsa_circ_212541,RMVar_hsa_circ_212539,RMVar_hsa_circ_344798,RMVar_hsa_circ_324668,RMVar_hsa_circ_354574,RMVar_hsa_circ_359426,RMVar_hsa_circ_350200,RMVar_hsa_circ_348569,RMVar_hsa_circ_212548,RMVar_hsa_circ_284959,RMVar_hsa_circ_333160,RMVar_hsa_circ_212549 8254 RMVar_ID_8254 Human_SNP_ID_696293873 A-to-I Human chr21 + 44075707 44075707 44075707 GGAGTCTCGCTGTATTGCCCAGGCTGGTCTCAAACTCCTGGCCTAAAGTGATCCTCCTGCCCTGG GGAGTCTCGCTGTATTGCCCAGGCTGGTCTCAGACTCCTGGCCTAAAGTGATCCTCCTGCCCTGG A G TRAPPC10 Ensembl:ENSG00000160218 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1021103946 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_212550,RMVar_hsa_circ_212538,RMVar_hsa_circ_87707,RMVar_hsa_circ_212534,RMVar_hsa_circ_60251,RMVar_hsa_circ_64013,RMVar_hsa_circ_316196,RMVar_hsa_circ_356808,RMVar_hsa_circ_362162,RMVar_hsa_circ_374841,RMVar_hsa_circ_309804,RMVar_hsa_circ_212540,RMVar_hsa_circ_212541,RMVar_hsa_circ_212539,RMVar_hsa_circ_344798,RMVar_hsa_circ_324668,RMVar_hsa_circ_354574,RMVar_hsa_circ_350200,RMVar_hsa_circ_212548,RMVar_hsa_circ_284959,RMVar_hsa_circ_333160,RMVar_hsa_circ_212549,RMVar_hsa_circ_21545,RMVar_hsa_circ_309149,RMVar_hsa_circ_325581,RMVar_hsa_circ_40093,RMVar_hsa_circ_11481,RMVar_hsa_circ_212551,RMVar_hsa_circ_375434 8255 RMVar_ID_8255 Human_SNP_ID_696298456 A-to-I Human chr21 + 44091579 44091579 44091579 CTCGTGCCTCAGCCTCCCGAGCAGCTGGGATTACAGACACGTGCCACCACGTCTGGCTAATTTTT CTCGTGCCTCAGCCTCCCGAGCAGCTGGGATTCCAGACACGTGCCACCACGTCTGGCTAATTTTT A C TRAPPC10 Ensembl:ENSG00000160218 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1195217821 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_354574,RMVar_hsa_circ_11481,RMVar_hsa_circ_339007,RMVar_hsa_circ_363053,RMVar_hsa_circ_65381,RMVar_hsa_circ_212555,RMVar_hsa_circ_23816,RMVar_hsa_circ_308999,RMVar_hsa_circ_340877,RMVar_hsa_circ_212558,RMVar_hsa_circ_212559,RMVar_hsa_circ_23342,RMVar_hsa_circ_310224,RMVar_hsa_circ_359952,RMVar_hsa_circ_212560 8256 RMVar_ID_8256 Human_SNP_ID_696312035 A-to-I Human chr21 - 44151525 44151525 44151525 CGTGGTGGCTTGTGCCTGTAGACCAGCTACTCAGGTGGCTGAGGCAGGAGAATCACTTGAACCCG CGTGGTGGCTTGTGCCTGTAGACCAGCTACTCCGGTGGCTGAGGCAGGAGAATCACTTGAACCCG T G - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1390591074 Functional Loss SNV dbSNP153 33..33 33 - - - 8257 RMVar_ID_8257 Human_SNP_ID_696312148 A-to-I Human chr21 - 44152207 44152207 44152207 AAAAAATACAAAAATTAGCTAGGTGCTGTGGCATGCGCCTGTGGTCCCAGCAACTCAGGAGGCTG AAAAAATACAAAAATTAGCTAGGTGCTGTGGCGTGCGCCTGTGGTCCCAGCAACTCAGGAGGCTG T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1473729267 Functional Loss SNV dbSNP153 33..33 33 - - - 8258 RMVar_ID_8258 Human_SNP_ID_696312202 A-to-I Human chr21 - 44152533 44152533 44152533 CTCCCACCTCAGTCTCCCAAAGTGTTGGGATTATAGGTATGAGCCACAATGCCTGGCCATTAATC CTCCCACCTCAGTCTCCCAAAGTGTTGGGATTGTAGGTATGAGCCACAATGCCTGGCCATTAATC T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1207742822 Functional Loss SNV dbSNP153 33..33 33 - - - 8259 RMVar_ID_8259 Human_SNP_ID_696326668 A-to-I Human chr21 - 44223982 44223982 44223982 GGGAGGCTGAGGCAGGAGAATTGCTTGAACCCAGGAGGCAGAGGTTGCAGTGGGCCAAGATGGCG GGGAGGCTGAGGCAGGAGAATTGCTTGAACCCGGGAGGCAGAGGTTGCAGTGGGCCAAGATGGCG T C ICOSLG Ensembl:ENSG00000160223 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1037342484 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_254873 8260 RMVar_ID_8260 Human_SNP_ID_696326795 A-to-I Human chr21 - 44224579 44224579 44224579 ATTCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGTGTGCGCCACCATGCCCAGGTAATTGTA ATTCTGCCTCAGCCTCCCAAGTAGCTGGGATTGCAGGTGTGCGCCACCATGCCCAGGTAATTGTA T C ICOSLG Ensembl:ENSG00000160223 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs750384285 Functional Loss SNV dbSNP153 33..33 33 - - - 8261 RMVar_ID_8261 Human_SNP_ID_696326796 A-to-I Human chr21 - 44224589 44224589 44224589 AACTCAAGCAATTCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGTGTGCGCCACCATGCCCA AACTCAAGCAATTCTGCCTCAGCCTCCCAAGTGGCTGGGATTACAGGTGTGCGCCACCATGCCCA T C ICOSLG Ensembl:ENSG00000160223 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223476320 Functional Loss SNV dbSNP153 33..33 33 - - - 8262 RMVar_ID_8262 Human_SNP_ID_696463490 A-to-I Human chr21 - 44677595 44677595 44677595 GGAATCTTTAAAAACTGATCACCCTGCAATTGATGAAGGAAAACCCACACCTGCACTTTCAGAAG GGAATCTTTAAAAACTGATCACCCTGCAATTGGTGAAGGAAAACCCACACCTGCACTTTCAGAAG T C TSPEAR,IMMTP1 Ensembl:ENSG00000175894,Ensembl:ENSG00000229880 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1320099090 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1839355 8263 RMVar_ID_8263 Human_SNP_ID_696495297 A-to-I Human chr21 - 44794699 44794699 44794699 AAACCCCCTCTCTACTAAAAATACAAAAAATTAGCTGGGCATGGTGGCGGACCCCTGTAGTCCCA AAACCCCCTCTCTACTAAAAATACAAAAAATTGGCTGGGCATGGTGGCGGACCCCTGTAGTCCCA T C UBE2G2 Ensembl:ENSG00000184787 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1383608252 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58483 8264 RMVar_ID_8264 Human_SNP_ID_696495380 A-to-I Human chr21 - 44795005 44795005 44795005 CCTCGCCTCCCAAAGTGCTGGGATTTACGGGCATGAGCCACAGCCCCCGGCCCTTACTGAGGTTT CCTCGCCTCCCAAAGTGCTGGGATTTACGGGCGTGAGCCACAGCCCCCGGCCCTTACTGAGGTTT T C UBE2G2 Ensembl:ENSG00000184787 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs561119890 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7052724,Human_RBP_ID_14344634,Human_RBP_ID_23185707 RMVar_hsa_circ_58483 8265 RMVar_ID_8265 Human_SNP_ID_696495402 A-to-I Human chr21 - 44795080 44795080 44795080 TTTTGTATTTTTAGTAGAAACGGGATTTCACTATGTTGGCTAGGCTGGTCTCTAACTCCTGACCT TTTTGTATTTTTAGTAGAAACGGGATTTCACTGTGTTGGCTAGGCTGGTCTCTAACTCCTGACCT T C UBE2G2 Ensembl:ENSG00000184787 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs973632343 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14344643 RMVar_hsa_circ_58483 8266 RMVar_ID_8266 Human_SNP_ID_696495404 A-to-I Human chr21 - 44795083 44795083 44795083 AATTTTTGTATTTTTAGTAGAAACGGGATTTCACTATGTTGGCTAGGCTGGTCTCTAACTCCTGA AATTTTTGTATTTTTAGTAGAAACGGGATTTCGCTATGTTGGCTAGGCTGGTCTCTAACTCCTGA T C UBE2G2 Ensembl:ENSG00000184787 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs540472532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14344645 RMVar_hsa_circ_58483 8267 RMVar_ID_8267 Human_SNP_ID_696495428 A-to-I Human chr21 - 44795176 44795176 44795176 TCACTGCAACATCTGCCTCCTGGCTTCAAGTAATTCTCCTGCCTCAGCTTCCCAAGTAGCTGGGG TCACTGCAACATCTGCCTCCTGGCTTCAAGTAGTTCTCCTGCCTCAGCTTCCCAAGTAGCTGGGG T C UBE2G2 Ensembl:ENSG00000184787 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215534265 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58483 8268 RMVar_ID_8268 Human_SNP_ID_696498354 A-to-I Human chr21 - 44806225 44806225 44806225 CCTGCTCAGTACCTGGCGTTGGTACACAGGCAAGGATTGGCACAACCAAAATTGGCCTTTTTCTC CCTGCTCAGTACCTGGCGTTGGTACACAGGCAGGGATTGGCACAACCAAAATTGGCCTTTTTCTC T C SUMO3 Ensembl:ENSG00000184900 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1198890121 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_573786,Human_RBP_ID_7052861,Human_RBP_ID_8206511,Human_RBP_ID_14345334,Human_RBP_ID_17284394,Human_RBP_ID_17397682,Human_RBP_ID_18327093,Human_RBP_ID_23930714 Human_miRNA_ID_1057907,Human_miRNA_ID_2490919,Human_miRNA_ID_2753009 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 8269 RMVar_ID_8269 Human_SNP_ID_696512809 A-to-I Human chr21 - 44852320 44852320 44852320 AAAATTAGCCAAGTATGGTGGTGGGTGCCTGCAGTCCTAGCTACCCGGAGGCTGAGGCAGGAGAA AAAATTAGCCAAGTATGGTGGTGGGTGCCTGCGGTCCTAGCTACCCGGAGGCTGAGGCAGGAGAA T C PTTG1IP Ensembl:ENSG00000183255 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs537797054 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17572470 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 8270 RMVar_ID_8270 Human_SNP_ID_696512816 A-to-I Human chr21 - 44852341 44852341 44852341 CCCGTCTCTACTAAAAATACAAAAATTAGCCAAGTATGGTGGTGGGTGCCTGCAGTCCTAGCTAC CCCGTCTCTACTAAAAATACAAAAATTAGCCACGTATGGTGGTGGGTGCCTGCAGTCCTAGCTAC T G PTTG1IP Ensembl:ENSG00000183255 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1044627116 Functional Loss SNV dbSNP153 33..33 33 - - - 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 8271 RMVar_ID_8271 Human_SNP_ID_696512922 A-to-I Human chr21 - 44852737 44852737 44852737 AACTGGAAGTAGACTCAGGAGCGAGTTTTTCAATAAGAACTTAACCAGCCTCCTTGCTAGTATCT AACTGGAAGTAGACTCAGGAGCGAGTTTTTCAGTAAGAACTTAACCAGCCTCCTTGCTAGTATCT T C PTTG1IP Ensembl:ENSG00000183255 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1344110 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_636,GWAS_ID_637,GWAS_ID_638,GWAS_ID_639,GWAS_ID_640,GWAS_ID_641 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 8272 RMVar_ID_8272 Human_SNP_ID_696513158 A-to-I Human chr21 - 44853432 44853432 44853432 GCGATGTCAGCTCACTGCAAGCTCTGCCTCCCAGGTTCACACCATTCTTCTGCCTCAGCCTCCTG GCGATGTCAGCTCACTGCAAGCTCTGCCTCCCGGGTTCACACCATTCTTCTGCCTCAGCCTCCTG T C PTTG1IP Ensembl:ENSG00000183255 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1423779313 Functional Loss SNV dbSNP153 33..33 33 - - - 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 8273 RMVar_ID_8273 Human_SNP_ID_696516699 A-to-I Human chr21 - 44864465 44864465 44864465 TTGAAACCGGAAGTCGGAGGTTGCAGTGAGCCAAGATTGTGCCACTGCACTCTAGCCTGGGCAAC TTGAAACCGGAAGTCGGAGGTTGCAGTGAGCCGAGATTGTGCCACTGCACTCTAGCCTGGGCAAC T C PTTG1IP Ensembl:ENSG00000183255 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1243245171 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14346533,Human_RBP_ID_25648107 RMVar_hsa_circ_12460,RMVar_hsa_circ_212605,RMVar_hsa_circ_104447,RMVar_hsa_circ_80161,RMVar_hsa_circ_122222,RMVar_hsa_circ_212604,RMVar_hsa_circ_212612 8274 RMVar_ID_8274 Human_SNP_ID_696516700 A-to-I Human chr21 - 44864465 44864465 44864465 TTGAAACCGGAAGTCGGAGGTTGCAGTGAGCCAAGATTGTGCCACTGCACTCTAGCCTGGGCAAC TTGAAACCGGAAGTCGGAGGTTGCAGTGAGCCCAGATTGTGCCACTGCACTCTAGCCTGGGCAAC T G PTTG1IP Ensembl:ENSG00000183255 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1243245171 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14346533,Human_RBP_ID_25648107 RMVar_hsa_circ_12460,RMVar_hsa_circ_212605,RMVar_hsa_circ_104447,RMVar_hsa_circ_80161,RMVar_hsa_circ_122222,RMVar_hsa_circ_212604,RMVar_hsa_circ_212612 8275 RMVar_ID_8275 Human_SNP_ID_696539196 A-to-I Human chr21 - 44937386 44937386 44937386 TCTTAGCCTCCTGAATAGCTGGGAACACAGGCATGTGCCACCACACCTGGCTAATTTTTTGGGTT TCTTAGCCTCCTGAATAGCTGGGAACACAGGCGTGTGCCACCACACCTGGCTAATTTTTTGGGTT T C LINC01547 Ensembl:ENSG00000183250 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs535222254 Functional Loss SNV dbSNP153 33..33 33 - - - 8276 RMVar_ID_8276 Human_SNP_ID_696576291 A-to-I Human chr21 + 45061327 45061327 45061327 TTGGGGCTTTTGGACTTATACTGAGCCACACTACCAGCACCCTAGTGTCTCTAGCTTGCAGATGG TTGGGGCTTTTGGACTTATACTGAGCCACACTGCCAGCACCCTAGTGTCTCTAGCTTGCAGATGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs753086496 Functional Loss SNV dbSNP153 33..33 33 - - - 8277 RMVar_ID_8277 Human_SNP_ID_696612807 A-to-I Human chr21 + 45204996 45204996 45204996 CTAGCCATTCATAGAAGAATTGATGGGTTCACACCTGTCATCCCAACACTTTGGGAGGCCAAGGC CTAGCCATTCATAGAAGAATTGATGGGTTCACGCCTGTCATCCCAACACTTTGGGAGGCCAAGGC A G ADARB1 Ensembl:ENSG00000197381 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569036717 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_212639,RMVar_hsa_circ_373075,RMVar_hsa_circ_95611,RMVar_hsa_circ_212641,RMVar_hsa_circ_212640,RMVar_hsa_circ_212645,RMVar_hsa_circ_376257 8278 RMVar_ID_8278 Human_SNP_ID_696628535 A-to-I Human chr21 - 45264689 45264641 45264690 CCACCCCTCCCTCGCCCCGACTGCCCCGCCCCACCCTCACCCCGACTGCCCCGCCCTCGCCCGGC CCACCCCTCCCTCGCCCCGACTGCCCCGCCC__________________________________ AGGGCAGGGACGGCCAGCCGGGCGAGGGCGGGGCAGTCGGGGTGAGGGTG A POFUT2 Ensembl:ENSG00000186866 Protein coding exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1301106015 Functional Loss DEL dbSNP153 32..65 33 - - - Human_RBP_ID_573993,Human_RBP_ID_5132789,Human_RBP_ID_17572576,Human_RBP_ID_18952065 8279 RMVar_ID_8279 Human_SNP_ID_696628546 A-to-I Human chr21 - 45264689 45264665 45264690 CCACCCCTCCCTCGCCCCGACTGCCCCGCCCCACCCTCACCCCGACTGCCCCGCCCTCGCCCGGC CCACCCCTCCCTCGCCCCGACTGCCCCGCCC_________________________TCGCCCGGC AGGGCGGGGCAGTCGGGGTGAGGGTG A POFUT2 Ensembl:ENSG00000186866 Protein coding exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs565644510 Functional Loss DEL dbSNP153 32..56 33 - - - Human_RBP_ID_573993,Human_RBP_ID_5132789,Human_RBP_ID_17572576,Human_RBP_ID_18952065 8280 RMVar_ID_8280 Human_SNP_ID_696628556 A-to-I Human chr21 - 45264689 45264689 45264689 CCACCCCTCCCTCGCCCCGACTGCCCCGCCCCACCCTCACCCCGACTGCCCCGCCCTCGCCCGGC CCACCCCTCCCTCGCCCCGACTGCCCCGCCCCTCCCTCACCCCGACTGCCCCGCCCTCGCCCGGC T A POFUT2 Ensembl:ENSG00000186866 Protein coding exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1173401943 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_573993,Human_RBP_ID_5132789,Human_RBP_ID_17572576,Human_RBP_ID_18952065 8281 RMVar_ID_8281 Human_SNP_ID_696628557 A-to-I Human chr21 - 45264689 45264689 45264689 CCACCCCTCCCTCGCCCCGACTGCCCCGCCCCACCCTCACCCCGACTGCCCCGCCCTCGCCCGGC CCACCCCTCCCTCGCCCCGACTGCCCCGCCCCCCCCTCACCCCGACTGCCCCGCCCTCGCCCGGC T G POFUT2 Ensembl:ENSG00000186866 Protein coding exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1173401943 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_573993,Human_RBP_ID_5132789,Human_RBP_ID_17572576,Human_RBP_ID_18952065 8282 RMVar_ID_8282 Human_SNP_ID_696849431 A-to-I Human chr21 + 46004262 46004262 46004262 GGGGCTCAGCCCTGAGCTAGTGTCACCTGCACAGGGCCCTCTGAGGCTCAGCCCTGAGCTGGCGT GGGGCTCAGCCCTGAGCTAGTGTCACCTGCACGGGGCCCTCTGAGGCTCAGCCCTGAGCTGGCGT A G COL6A1 Ensembl:ENSG00000142156 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs943264596 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5529714,Human_RBP_ID_18783083 Human_miRNA_ID_865333,Human_miRNA_ID_976691,Human_miRNA_ID_2209630,Human_miRNA_ID_3034236 RMVar_hsa_circ_80310,RMVar_hsa_circ_212667,RMVar_hsa_circ_113830,RMVar_hsa_circ_93324,RMVar_hsa_circ_212670,RMVar_hsa_circ_111153,RMVar_hsa_circ_212671,RMVar_hsa_circ_116940,RMVar_hsa_circ_212672,RMVar_hsa_circ_92758,RMVar_hsa_circ_95517,RMVar_hsa_circ_212673,RMVar_hsa_circ_212674,RMVar_hsa_circ_81611,RMVar_hsa_circ_212675,RMVar_hsa_circ_212676,RMVar_hsa_circ_92068,RMVar_hsa_circ_113047,RMVar_hsa_circ_95327,RMVar_hsa_circ_212678,RMVar_hsa_circ_212679,RMVar_hsa_circ_124456,RMVar_hsa_circ_114445,RMVar_hsa_circ_212680,RMVar_hsa_circ_212681,RMVar_hsa_circ_212682,RMVar_hsa_circ_105362,RMVar_hsa_circ_212683,RMVar_hsa_circ_120623,RMVar_hsa_circ_104192,RMVar_hsa_circ_212684,RMVar_hsa_circ_99785,RMVar_hsa_circ_212685,RMVar_hsa_circ_110062,RMVar_hsa_circ_212686,RMVar_hsa_circ_212687 8283 RMVar_ID_8283 Human_SNP_ID_696911611 A-to-I Human chr21 + 46186077 46186077 46186077 AAACTGAAACTTTCTGCTCTGCAAAGAATGTCAAGAAAATGAAAAGACAAGTCAGAGACTGGGAG AAACTGAAACTTTCTGCTCTGCAAAGAATGTCGAGAAAATGAAAAGACAAGTCAGAGACTGGGAG A G AP001468.1 Ensembl:ENSG00000228404 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1368979082 Functional Loss SNV dbSNP153 33..33 33 - - - 8284 RMVar_ID_8284 Human_SNP_ID_696916429 A-to-I Human chr21 + 46200538 46200538 46200538 CTGCAATCTTCCTGACAAAAATGTAGTTTCATAACCTGAATCTAATCACGAGACACCAGAAAAAA CTGCAATCTTCCTGACAAAAATGTAGTTTCATGACCTGAATCTAATCACGAGACACCAGAAAAAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs767025699 Functional Loss SNV dbSNP153 33..33 33 - - - 8285 RMVar_ID_8285 Human_SNP_ID_696916728 A-to-I Human chr21 - 46201828 46201828 46201828 GTGCCACTGCACTCCAGCCTAGGCGAGAGTGCAAGACACCGTCTCAAAAAAAAAAAAAAGATTTT GTGCCACTGCACTCCAGCCTAGGCGAGAGTGCGAGACACCGTCTCAAAAAAAAAAAAAAGATTTT T C LSS Ensembl:ENSG00000160285 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs544319185 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22723821 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 8286 RMVar_ID_8286 Human_SNP_ID_696916807 A-to-I Human chr21 - 46202083 46202083 46202083 GCCTATATTAAGATTTTAAACTTGCCGGGCGCAGTGGCTGACGCCTGTAATCCCAGCACTTTGGG GCCTATATTAAGATTTTAAACTTGCCGGGCGCGGTGGCTGACGCCTGTAATCCCAGCACTTTGGG T C LSS Ensembl:ENSG00000160285 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1373180396 Functional Loss SNV dbSNP153 33..33 33 - - - 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 8287 RMVar_ID_8287 Human_SNP_ID_696927821 A-to-I Human chr21 + 46237611 46237610 46237611 GTAGAAACGGGATTTTGCTGTATTGTCAGGCTAGTCTACAACTCCTGAACTCAAGTGATGTGCAC GTAGAAACGGGATTTTGCTGTATTGTCAGGCT_GTCTACAACTCCTGAACTCAAGTGATGTGCAC TA T MCM3AP-AS1 Ensembl:ENSG00000215424 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1346890648 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_212719,RMVar_hsa_circ_266323 8288 RMVar_ID_8288 Human_SNP_ID_696930893 A-to-I Human chr21 + 46249353 46249353 46249353 AGAACTACAGGCACACACCACCATGCCCAGCTAATTTTTGTATTTTTTATAGAGACAGGGTTTCA AGAACTACAGGCACACACCACCATGCCCAGCTCATTTTTGTATTTTTTATAGAGACAGGGTTTCA A C MCM3AP-AS1 Ensembl:ENSG00000215424 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1410835703 Functional Loss SNV dbSNP153 33..33 33 - - - 8289 RMVar_ID_8289 Human_SNP_ID_696931763 A-to-I Human chr21 + 46252568 46252568 46252568 AAACTAAGCTGGGCGTGGTGGTGTGCGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAAA AAACTAAGCTGGGCGTGGTGGTGTGCGCCTGTCATCCCAGCTACTTGGGAGGCTGAGGCAGGAAA A C MCM3AP-AS1 Ensembl:ENSG00000215424 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264465698 Functional Loss SNV dbSNP153 33..33 33 - - - 8290 RMVar_ID_8290 Human_SNP_ID_696931843 A-to-I Human chr21 + 46252941 46252941 46252941 GAAGCATGCAGATTGCTTGAGCCCAGGAGTTCAAGACCAGCTTGGGCAACATAGTGAAACCCCAT GAAGCATGCAGATTGCTTGAGCCCAGGAGTTCTAGACCAGCTTGGGCAACATAGTGAAACCCCAT A T MCM3AP-AS1 Ensembl:ENSG00000215424 lincRNA intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs942420631 Functional Loss SNV dbSNP153 33..33 33 - - - 8291 RMVar_ID_8291 Human_SNP_ID_696936769 A-to-I Human chr21 - 46268799 46268799 46268799 CCTCAGGTGATCCACCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAACCACCTTGCC CCTCAGGTGATCCACCCACCTCGGCCTCCCAATGTGCTGGGATTACAGGCATGAACCACCTTGCC T A MCM3AP Ensembl:ENSG00000160294 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1373727585 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36134,RMVar_hsa_circ_212720,RMVar_hsa_circ_89774,RMVar_hsa_circ_45864,RMVar_hsa_circ_43498,RMVar_hsa_circ_115234,RMVar_hsa_circ_93587,RMVar_hsa_circ_74637,RMVar_hsa_circ_212723,RMVar_hsa_circ_212724,RMVar_hsa_circ_376580,RMVar_hsa_circ_7301,RMVar_hsa_circ_355546,RMVar_hsa_circ_320105,RMVar_hsa_circ_23958,RMVar_hsa_circ_320147,RMVar_hsa_circ_212726,RMVar_hsa_circ_87720 8292 RMVar_ID_8292 Human_SNP_ID_696936782 A-to-I Human chr21 - 46268839 46268839 46268839 GGATTTCGCCATGCTGGCCAGGCTGATCTCGAACTCCTAGCCTCAGGTGATCCACCCACCTCGGC GGATTTCGCCATGCTGGCCAGGCTGATCTCGAGCTCCTAGCCTCAGGTGATCCACCCACCTCGGC T C MCM3AP Ensembl:ENSG00000160294 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1274700786 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36134,RMVar_hsa_circ_212720,RMVar_hsa_circ_89774,RMVar_hsa_circ_45864,RMVar_hsa_circ_43498,RMVar_hsa_circ_115234,RMVar_hsa_circ_93587,RMVar_hsa_circ_74637,RMVar_hsa_circ_212723,RMVar_hsa_circ_212724,RMVar_hsa_circ_376580,RMVar_hsa_circ_7301,RMVar_hsa_circ_355546,RMVar_hsa_circ_320105,RMVar_hsa_circ_23958,RMVar_hsa_circ_320147,RMVar_hsa_circ_212726,RMVar_hsa_circ_87720 8293 RMVar_ID_8293 Human_SNP_ID_696936790 A-to-I Human chr21 - 46268878 46268878 46268878 AGGAGCCCGCCACCACGCCCAGCTAACTTAGTAGAGATGGGATTTCGCCATGCTGGCCAGGCTGA AGGAGCCCGCCACCACGCCCAGCTAACTTAGTGGAGATGGGATTTCGCCATGCTGGCCAGGCTGA T C MCM3AP Ensembl:ENSG00000160294 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs1283645205 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14359491,Human_RBP_ID_17572475 RMVar_hsa_circ_36134,RMVar_hsa_circ_212720,RMVar_hsa_circ_89774,RMVar_hsa_circ_45864,RMVar_hsa_circ_43498,RMVar_hsa_circ_115234,RMVar_hsa_circ_93587,RMVar_hsa_circ_74637,RMVar_hsa_circ_212723,RMVar_hsa_circ_212724,RMVar_hsa_circ_376580,RMVar_hsa_circ_7301,RMVar_hsa_circ_355546,RMVar_hsa_circ_320105,RMVar_hsa_circ_23958,RMVar_hsa_circ_320147,RMVar_hsa_circ_212726,RMVar_hsa_circ_87720 8294 RMVar_ID_8294 Human_SNP_ID_696936918 A-to-I Human chr21 - 46269316 46269316 46269316 GCTCAGGAGTTCAAGGCCAGCCTGGGCAACATAGGGAGGCCCTGTCTCTACTAAAAATAAAAAAA GCTCAGGAGTTCAAGGCCAGCCTGGGCAACATGGGGAGGCCCTGTCTCTACTAAAAATAAAAAAA T C MCM3AP Ensembl:ENSG00000160294 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1280573769 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36134,RMVar_hsa_circ_212720,RMVar_hsa_circ_89774,RMVar_hsa_circ_45864,RMVar_hsa_circ_43498,RMVar_hsa_circ_115234,RMVar_hsa_circ_93587,RMVar_hsa_circ_74637,RMVar_hsa_circ_212723,RMVar_hsa_circ_212724,RMVar_hsa_circ_376580,RMVar_hsa_circ_7301,RMVar_hsa_circ_355546,RMVar_hsa_circ_320105,RMVar_hsa_circ_23958,RMVar_hsa_circ_320147,RMVar_hsa_circ_212726,RMVar_hsa_circ_87720 8295 RMVar_ID_8295 Human_SNP_ID_696936920 A-to-I Human chr21 - 46269320 46269320 46269320 TTGAGCTCAGGAGTTCAAGGCCAGCCTGGGCAACATAGGGAGGCCCTGTCTCTACTAAAAATAAA TTGAGCTCAGGAGTTCAAGGCCAGCCTGGGCAGCATAGGGAGGCCCTGTCTCTACTAAAAATAAA T C MCM3AP Ensembl:ENSG00000160294 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1267178487 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36134,RMVar_hsa_circ_212720,RMVar_hsa_circ_89774,RMVar_hsa_circ_45864,RMVar_hsa_circ_43498,RMVar_hsa_circ_115234,RMVar_hsa_circ_93587,RMVar_hsa_circ_74637,RMVar_hsa_circ_212723,RMVar_hsa_circ_212724,RMVar_hsa_circ_376580,RMVar_hsa_circ_7301,RMVar_hsa_circ_355546,RMVar_hsa_circ_320105,RMVar_hsa_circ_23958,RMVar_hsa_circ_320147,RMVar_hsa_circ_212726,RMVar_hsa_circ_87720 8296 RMVar_ID_8296 Human_SNP_ID_696937406 A-to-I Human chr21 - 46271237 46271237 46271237 GGGTTGCTTGAGGCCAGGAGGTTGAAGCTGCAATGAACTGTGATTGTGCCAGTGCACTCCAGCCT GGGTTGCTTGAGGCCAGGAGGTTGAAGCTGCAGTGAACTGTGATTGTGCCAGTGCACTCCAGCCT T C MCM3AP Ensembl:ENSG00000160294 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1478793109 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14359636 RMVar_hsa_circ_36134,RMVar_hsa_circ_212720,RMVar_hsa_circ_89774,RMVar_hsa_circ_45864,RMVar_hsa_circ_43498,RMVar_hsa_circ_115234,RMVar_hsa_circ_93587,RMVar_hsa_circ_212723,RMVar_hsa_circ_212724,RMVar_hsa_circ_376580,RMVar_hsa_circ_7301,RMVar_hsa_circ_355546,RMVar_hsa_circ_320105,RMVar_hsa_circ_23958,RMVar_hsa_circ_320147,RMVar_hsa_circ_65822,RMVar_hsa_circ_212726,RMVar_hsa_circ_87720,RMVar_hsa_circ_358902,RMVar_hsa_circ_362633,RMVar_hsa_circ_53591 8297 RMVar_ID_8297 Human_SNP_ID_696939431 A-to-I Human chr21 - 46278140 46278140 46278140 TTTTTTTTCGGGGGGTGGTAAGTTAGAGTCTCACTCTGTCACCCAGGCTGGAGAGCAGCAGTGTA TTTTTTTTCGGGGGGTGGTAAGTTAGAGTCTCCCTCTGTCACCCAGGCTGGAGAGCAGCAGTGTA T G MCM3AP Ensembl:ENSG00000160294 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs919069978 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14359922 RMVar_hsa_circ_93587,RMVar_hsa_circ_6185,RMVar_hsa_circ_212723,RMVar_hsa_circ_376580,RMVar_hsa_circ_23958,RMVar_hsa_circ_21586,RMVar_hsa_circ_212726,RMVar_hsa_circ_87720,RMVar_hsa_circ_362633,RMVar_hsa_circ_53591,RMVar_hsa_circ_345856,RMVar_hsa_circ_103936,RMVar_hsa_circ_310291,RMVar_hsa_circ_212727,RMVar_hsa_circ_356467,RMVar_hsa_circ_21789,RMVar_hsa_circ_212730,RMVar_hsa_circ_93815,RMVar_hsa_circ_212729,RMVar_hsa_circ_312184,RMVar_hsa_circ_212731,RMVar_hsa_circ_212732,RMVar_hsa_circ_320289,RMVar_hsa_circ_324660,RMVar_hsa_circ_212733 8298 RMVar_ID_8298 Human_SNP_ID_696939650 A-to-I Human chr21 - 46278812 46278812 46278812 AAAATTAGCCGGGCATGGTGGCAGGTGCCTGTAGTCCCAGCTACTTGTGAGGCTGAGGCAGGAGA AAAATTAGCCGGGCATGGTGGCAGGTGCCTGTGGTCCCAGCTACTTGTGAGGCTGAGGCAGGAGA T C MCM3AP Ensembl:ENSG00000160294 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs976124119 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93587,RMVar_hsa_circ_6185,RMVar_hsa_circ_212723,RMVar_hsa_circ_376580,RMVar_hsa_circ_23958,RMVar_hsa_circ_21586,RMVar_hsa_circ_212726,RMVar_hsa_circ_87720,RMVar_hsa_circ_362633,RMVar_hsa_circ_53591,RMVar_hsa_circ_345856,RMVar_hsa_circ_103936,RMVar_hsa_circ_310291,RMVar_hsa_circ_212727,RMVar_hsa_circ_356467,RMVar_hsa_circ_21789,RMVar_hsa_circ_212730,RMVar_hsa_circ_93815,RMVar_hsa_circ_212729,RMVar_hsa_circ_312184,RMVar_hsa_circ_212731,RMVar_hsa_circ_212732,RMVar_hsa_circ_320289,RMVar_hsa_circ_324660,RMVar_hsa_circ_212733 8299 RMVar_ID_8299 Human_SNP_ID_696939673 A-to-I Human chr21 - 46278854 46278854 46278854 CCTGGCTGATATGGTGAAACCCCATCTCTACTAAAAATACAAAAAATTAGCCGGGCATGGTGGCA CCTGGCTGATATGGTGAAACCCCATCTCTACTGAAAATACAAAAAATTAGCCGGGCATGGTGGCA T C MCM3AP Ensembl:ENSG00000160294 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs942779865 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93587,RMVar_hsa_circ_6185,RMVar_hsa_circ_212723,RMVar_hsa_circ_376580,RMVar_hsa_circ_23958,RMVar_hsa_circ_21586,RMVar_hsa_circ_212726,RMVar_hsa_circ_87720,RMVar_hsa_circ_362633,RMVar_hsa_circ_53591,RMVar_hsa_circ_345856,RMVar_hsa_circ_103936,RMVar_hsa_circ_310291,RMVar_hsa_circ_212727,RMVar_hsa_circ_356467,RMVar_hsa_circ_21789,RMVar_hsa_circ_212730,RMVar_hsa_circ_93815,RMVar_hsa_circ_212729,RMVar_hsa_circ_312184,RMVar_hsa_circ_212731,RMVar_hsa_circ_212732,RMVar_hsa_circ_320289,RMVar_hsa_circ_324660,RMVar_hsa_circ_212733 8300 RMVar_ID_8300 Human_SNP_ID_696939793 A-to-I Human chr21 - 46279144 46279144 46279144 AGCTGAGATTACAGGTGCGCTCCACCACGCCCAGCTAATATTTTTGTATTTTTAGTAGAGATGGG AGCTGAGATTACAGGTGCGCTCCACCACGCCCGGCTAATATTTTTGTATTTTTAGTAGAGATGGG T C MCM3AP Ensembl:ENSG00000160294 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1216460009 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25652866 RMVar_hsa_circ_93587,RMVar_hsa_circ_6185,RMVar_hsa_circ_212723,RMVar_hsa_circ_376580,RMVar_hsa_circ_23958,RMVar_hsa_circ_21586,RMVar_hsa_circ_212726,RMVar_hsa_circ_87720,RMVar_hsa_circ_362633,RMVar_hsa_circ_53591,RMVar_hsa_circ_345856,RMVar_hsa_circ_103936,RMVar_hsa_circ_310291,RMVar_hsa_circ_212727,RMVar_hsa_circ_356467,RMVar_hsa_circ_21789,RMVar_hsa_circ_212730,RMVar_hsa_circ_93815,RMVar_hsa_circ_212729,RMVar_hsa_circ_312184,RMVar_hsa_circ_212731,RMVar_hsa_circ_212732,RMVar_hsa_circ_320289,RMVar_hsa_circ_324660,RMVar_hsa_circ_212733 8301 RMVar_ID_8301 Human_SNP_ID_696943040 A-to-I Human chr21 + 46288558 46288558 46288558 AAAGTTAGCTGGGTGTGGTGGCATTTGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAAA AAAGTTAGCTGGGTGTGGTGGCATTTGCCTGTTATCCCAGCTACTCGGGAGGCTGAGGCAGGAAA A T YBEY Ensembl:ENSG00000182362 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs533941735 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77535,RMVar_hsa_circ_212736 8302 RMVar_ID_8302 Human_SNP_ID_696943630 A-to-I Human chr21 + 46290406 46290406 46290406 TTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGTCAGGCTGGTGTCAAACCCCTGACCT TTTTGTATTTTTAGTAGAGATGGGGTTTCACCGTGTTGGTCAGGCTGGTGTCAAACCCCTGACCT A G YBEY Ensembl:ENSG00000182362 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1363701471 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77535,RMVar_hsa_circ_212736 8303 RMVar_ID_8303 Human_SNP_ID_696947311 A-to-I Human chr21 - 46299127 46299127 46299127 CCTGTCTCTACTAAGAAATACAAAAATTAGCCAGGTGTGGTGGCACACACATGTAGTACAAGCTA CCTGTCTCTACTAAGAAATACAAAAATTAGCCGGGTGTGGTGGCACACACATGTAGTACAAGCTA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1489553301 Functional Loss SNV dbSNP153 33..33 33 - - - 8304 RMVar_ID_8304 Human_SNP_ID_696953436 A-to-I Human chr21 - 46319606 46319606 46319606 GCATGAGCCACCGCACCTGGCCCTTTTTTATTATTTTTTATAGAGATGGGGTCTTGTTGTGTTGT GCATGAGCCACCGCACCTGGCCCTTTTTTATTGTTTTTTATAGAGATGGGGTCTTGTTGTGTTGT T C C21orf58 Ensembl:ENSG00000160298 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1386602579 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7054270 RMVar_hsa_circ_89815,RMVar_hsa_circ_212741 8305 RMVar_ID_8305 Human_SNP_ID_696953445 A-to-I Human chr21 - 46319636 46319636 46319636 CCTCAGCCTCCCTAAGTGCTGGGATTACAGGCATGAGCCACCGCACCTGGCCCTTTTTTATTATT CCTCAGCCTCCCTAAGTGCTGGGATTACAGGCGTGAGCCACCGCACCTGGCCCTTTTTTATTATT T C C21orf58 Ensembl:ENSG00000160298 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs74888598 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89815,RMVar_hsa_circ_212741 8306 RMVar_ID_8306 Human_SNP_ID_696953446 A-to-I Human chr21 - 46319636 46319636 46319636 CCTCAGCCTCCCTAAGTGCTGGGATTACAGGCATGAGCCACCGCACCTGGCCCTTTTTTATTATT CCTCAGCCTCCCTAAGTGCTGGGATTACAGGCCTGAGCCACCGCACCTGGCCCTTTTTTATTATT T G C21orf58 Ensembl:ENSG00000160298 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs74888598 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89815,RMVar_hsa_circ_212741 8307 RMVar_ID_8307 Human_SNP_ID_696953473 A-to-I Human chr21 - 46319733 46319733 46319733 ACCACGACGCCTGGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGT ACCACGACGCCTGGCTAATTTTTTGTATTTTTGGTAGAGACGGGGTTTCACCATGTTGGCCAGGT T C C21orf58 Ensembl:ENSG00000160298 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs925526801 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89815,RMVar_hsa_circ_212741 8308 RMVar_ID_8308 Human_SNP_ID_696953502 A-to-I Human chr21 - 46319810 46319810 46319810 TCACTGCAAACTCTGCCTTCCGATTTCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGA TCACTGCAAACTCTGCCTTCCGATTTCAAGCAGTTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGA T C C21orf58 Ensembl:ENSG00000160298 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1298880298 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25652912 RMVar_hsa_circ_89815,RMVar_hsa_circ_212741 8309 RMVar_ID_8309 Human_SNP_ID_696953503 A-to-I Human chr21 - 46319811 46319811 46319811 GTCACTGCAAACTCTGCCTTCCGATTTCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGG GTCACTGCAAACTCTGCCTTCCGATTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGG T C C21orf58 Ensembl:ENSG00000160298 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1386186324 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14361344,Human_RBP_ID_25652912 RMVar_hsa_circ_89815,RMVar_hsa_circ_212741 8310 RMVar_ID_8310 Human_SNP_ID_696953650 A-to-I Human chr21 - 46320306 46320306 46320306 TTGAGGTCAGGAGTTCGAGACCAGTCTGGCCAACATGGTGAAACCCCATCTCTACCAAAAATACA TTGAGGTCAGGAGTTCGAGACCAGTCTGGCCAGCATGGTGAAACCCCATCTCTACCAAAAATACA T C C21orf58 Ensembl:ENSG00000160298 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs529624705 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89815,RMVar_hsa_circ_212741 8311 RMVar_ID_8311 Human_SNP_ID_696954029 A-to-I Human chr21 - 46321336 46321336 46321336 AATGGGCCAGGTGCACTGGCTTTCACTCAAAAATTAGCTGGGCATGATGGCACGTACCTGTAGTC AATGGGCCAGGTGCACTGGCTTTCACTCAAAATTTAGCTGGGCATGATGGCACGTACCTGTAGTC T A C21orf58 Ensembl:ENSG00000160298 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs944152579 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1606911,Human_RBP_ID_1939027,Human_RBP_ID_14361460,Human_RBP_ID_18327246,Human_RBP_ID_25649363,Human_RBP_ID_27030336,Human_RBP_ID_27491018 8312 RMVar_ID_8312 Human_SNP_ID_696954283 A-to-I Human chr21 - 46322225 46322225 46322225 TAGAGTGCAGTGGTGAGACCACCGCTCATTGCAGCCTCAACTTCCCCGGGCTCAGGTGATTCTCC TAGAGTGCAGTGGTGAGACCACCGCTCATTGCTGCCTCAACTTCCCCGGGCTCAGGTGATTCTCC T A C21orf58 Ensembl:ENSG00000160298 Protein coding intron GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831 HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line - 29129909,32596459 RNA-Seq:(High) rs1175992723 Functional Loss SNV dbSNP153 33..33 33 - - - 8313 RMVar_ID_8313 Human_SNP_ID_696954482 A-to-I Human chr21 - 46322738 46322738 46322738 CAGTCTCGCTGCGACGCCCAGGCTATAGCGCAATGGCGCGATCTCGGCTCCCTGCAACCTCCCTC CAGTCTCGCTGCGACGCCCAGGCTATAGCGCAGTGGCGCGATCTCGGCTCCCTGCAACCTCCCTC T C C21orf58 Ensembl:ENSG00000160298 Protein coding start codon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973911404 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14361595,Human_RBP_ID_22265045,Human_RBP_ID_22819143,Human_RBP_ID_23010336,Human_RBP_ID_27303507,Human_RBP_ID_27491038 Human_Splice_Rec_2132655,Human_Splice_Rec_2132669,Human_Splice_Rec_2132715,Human_Splice_Rec_2132725 8314 RMVar_ID_8314 Human_SNP_ID_696971908 A-to-I Human chr21 + 46373756 46373756 46373756 CTTAGCTTTTTTTTTTTTTTTTTTTTGGGCGGAGTCTCGCTCTGTCGCCAGGCTGGAGTGCAGTG CTTAGCTTTTTTTTTTTTTTTTTTTTGGGCGGGGTCTCGCTCTGTCGCCAGGCTGGAGTGCAGTG A G PCNT Ensembl:ENSG00000160299 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264648076 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64540,RMVar_hsa_circ_358615,RMVar_hsa_circ_52454,RMVar_hsa_circ_59616,RMVar_hsa_circ_37161,RMVar_hsa_circ_347486,RMVar_hsa_circ_305208,RMVar_hsa_circ_330247,RMVar_hsa_circ_212748,RMVar_hsa_circ_212747,RMVar_hsa_circ_90400 8315 RMVar_ID_8315 Human_SNP_ID_696987295 A-to-I Human chr21 + 46417645 46417645 46417645 TAAAAATCAGGTATGGTTGGGCTCATGCTTGTAGTCTCAGCACTTTGGGAGGCTGAGGCGGGAGG TAAAAATCAGGTATGGTTGGGCTCATGCTTGTGGTCTCAGCACTTTGGGAGGCTGAGGCGGGAGG A G PCNT Ensembl:ENSG00000160299 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1415013675 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57716,RMVar_hsa_circ_65299,RMVar_hsa_circ_30224,RMVar_hsa_circ_212756,RMVar_hsa_circ_371395,RMVar_hsa_circ_47853,RMVar_hsa_circ_23620 8316 RMVar_ID_8316 Human_SNP_ID_696988917 A-to-I Human chr21 + 46422990 46422990 46422990 CTTTATTTGGCTGGGCACGGTGGCTCATGCCTATGATCCCAGCACTTCGGGAGGCTGAGACAGGA CTTTATTTGGCTGGGCACGGTGGCTCATGCCTGTGATCCCAGCACTTCGGGAGGCTGAGACAGGA A G PCNT Ensembl:ENSG00000160299 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs907952679 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_245291,Human_RBP_ID_14364509 RMVar_hsa_circ_40539,RMVar_hsa_circ_23620 8317 RMVar_ID_8317 Human_SNP_ID_696992509 A-to-I Human chr21 + 46432648 46432648 46432648 GTCTCTTCATTTAATTAGGATTTTTTTGAGATAGGGTCTGGCTCTGTCACCCAGGCTGGAGTGCA GTCTCTTCATTTAATTAGGATTTTTTTGAGATGGGGTCTGGCTCTGTCACCCAGGCTGGAGTGCA A G PCNT Ensembl:ENSG00000160299 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1185436611 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14365000 RMVar_hsa_circ_6618,RMVar_hsa_circ_40539,RMVar_hsa_circ_30429,RMVar_hsa_circ_39528 8318 RMVar_ID_8318 Human_SNP_ID_696992572 A-to-I Human chr21 + 46432855 46432855 46432855 GTTGGCCAGGCTGGTCTCAAACTTCTGACCTCAGGTGATCCGCCCGCCTGGGCCTCTCAGACTGC GTTGGCCAGGCTGGTCTCAAACTTCTGACCTCCGGTGATCCGCCCGCCTGGGCCTCTCAGACTGC A C PCNT Ensembl:ENSG00000160299 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1266078107 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6618,RMVar_hsa_circ_40539,RMVar_hsa_circ_30429,RMVar_hsa_circ_39528 8319 RMVar_ID_8319 Human_SNP_ID_696999881 A-to-I Human chr21 - 46457136 46457136 46457136 CCCAAACTGCCTTAAACCTTTTTTTCGTAGACAGTGTCTCACTCTGTTGCCCAGGCTGGAGTGCA CCCAAACTGCCTTAAACCTTTTTTTCGTAGACGGTGTCTCACTCTGTTGCCCAGGCTGGAGTGCA T C lnc-C21orf58-1,lnc-C21orf58-1:2,lnc-C21orf58-1:3,lnc-C21orf58-1:4,lnc-C21orf58-1:5,lnc-C21orf58-1:6,lnc-C21orf58-1:7,lnc-C21orf58-1:8,lnc-C21orf58-1:9,lnc-C21orf58-1:10 RNACentral:URS0000D5B19B,RNACentral:URS00008B34DD,RNACentral:URS00008BB56B,RNACentral:URS00009AEF0A,RNACentral:URS0000D5D3DE,RNACentral:URS0000D57D6E,RNACentral:URS0000D58AB2,RNACentral:URS0000D5AD8C,RNACentral:URS0000D59C38,RNACentral:URS0000D5AF1E lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,exon,exon,intron,intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1443951235 Functional Loss SNV dbSNP153 33..33 33 - - - 8320 RMVar_ID_8320 Human_SNP_ID_697015235 A-to-I Human chr21 + 46513690 46513690 46513690 GAATTAATGTTTTATAGGTTGAGAGCATCCCAAATATGAAAATCCAAAATCCAAAATGCTCTAAA GAATTAATGTTTTATAGGTTGAGAGCATCCCAGATATGAAAATCCAAAATCCAAAATGCTCTAAA A G DIP2A Ensembl:ENSG00000160305 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1172252834 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9336,RMVar_hsa_circ_79643,RMVar_hsa_circ_122861,RMVar_hsa_circ_212758,RMVar_hsa_circ_212759,RMVar_hsa_circ_14632,RMVar_hsa_circ_25996,RMVar_hsa_circ_317321,RMVar_hsa_circ_212770,RMVar_hsa_circ_286859,RMVar_hsa_circ_5245,RMVar_hsa_circ_212769,RMVar_hsa_circ_212772,RMVar_hsa_circ_285720,RMVar_hsa_circ_84759,RMVar_hsa_circ_337593,RMVar_hsa_circ_212771 8321 RMVar_ID_8321 Human_SNP_ID_697028967 A-to-I Human chr21 - 46563880 46563880 46563880 CCAAGGGTCCTTTGGTCTCGGTGTGTGCGATGATGACCTTCACGCCGGGGAGGATCTGGAAGGAG CCAAGGGTCCTTTGGTCTCGGTGTGTGCGATGCTGACCTTCACGCCGGGGAGGATCTGGAAGGAG T G - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs762345432 Functional Loss SNV dbSNP153 33..33 33 - - - 8322 RMVar_ID_8322 Human_SNP_ID_118910740 A-to-I Human chr2 - 240003142 240003142 240003142 AAACAGAATGTGTAATAAGTTTACTTCTGGCCAGGCAGCGTTCACGTCTGTAAACCCAGCACGTT AAACAGAATGTGTAATAAGTTTACTTCTGGCCGGGCAGCGTTCACGTCTGTAAACCCAGCACGTT T C NDUFA10 Ensembl:ENSG00000130414 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs565352393 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13817116 RMVar_hsa_circ_207936,RMVar_hsa_circ_67450,RMVar_hsa_circ_82546,RMVar_hsa_circ_207931,RMVar_hsa_circ_273120,RMVar_hsa_circ_278644,RMVar_hsa_circ_344547,RMVar_hsa_circ_367995,RMVar_hsa_circ_285623,RMVar_hsa_circ_274735,RMVar_hsa_circ_64844,RMVar_hsa_circ_271956,RMVar_hsa_circ_207938,RMVar_hsa_circ_207939,RMVar_hsa_circ_207937,RMVar_hsa_circ_207934,RMVar_hsa_circ_207935,RMVar_hsa_circ_207933 8323 RMVar_ID_8323 Human_SNP_ID_119042647 A-to-I Human chr2 - 240475765 240475765 240475765 TTTATATATTTATGGTATTCAGTATATATTCTAAAAGTTCCACCAAAAAACCTGTTAGACGTAAT TTTATATATTTATGGTATTCAGTATATATTCTGAAAGTTCCACCAAAAAACCTGTTAGACGTAAT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903216828 Functional Loss SNV dbSNP153 33..33 33 - - - 8324 RMVar_ID_8324 Human_SNP_ID_119043033 A-to-I Human chr2 - 240477520 240477520 240477520 TGTGGTCGCACACACCGTAGTCCCAGCTACTCAGGAGGCTGTGGTGGGAGGATTGCTTGAACTAG TGTGGTCGCACACACCGTAGTCCCAGCTACTCCGGAGGCTGTGGTGGGAGGATTGCTTGAACTAG T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1314420229 Functional Loss SNV dbSNP153 33..33 33 - - - 8325 RMVar_ID_8325 Human_SNP_ID_119043041 A-to-I Human chr2 - 240477543 240477543 240477543 CTAAAAAAAAGATCTTAGTCAGGTGTGGTCGCACACACCGTAGTCCCAGCTACTCAGGAGGCTGT CTAAAAAAAAGATCTTAGTCAGGTGTGGTCGCGCACACCGTAGTCCCAGCTACTCAGGAGGCTGT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs371043570 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2632004 8326 RMVar_ID_8326 Human_SNP_ID_119111333 A-to-I Human chr2 - 240717046 240717046 240717046 CTAATATTTTTTTAAGCATAGACAGACTTATAATTAATATACGTTAGTTAGTGACATTGAAACAG CTAATATTTTTTTAAGCATAGACAGACTTATAGTTAATATACGTTAGTTAGTGACATTGAAACAG T C KIF1A Ensembl:ENSG00000130294 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1215372721 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_546850,Human_RBP_ID_17506702,Human_RBP_ID_17953613,Human_RBP_ID_18315688,Human_RBP_ID_23861538,Human_RBP_ID_24421406 Human_miRNA_ID_1333942,Human_miRNA_ID_2659202 RMVar_hsa_circ_102481,RMVar_hsa_circ_207987 8327 RMVar_ID_8327 Human_SNP_ID_119207814 A-to-I Human chr2 + 241055037 241055037 241055037 TACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAGCCTGGGAGGCGGAGGTTGCAGTGAGGTGAGA TACTCAGGAGGCTGAGGCAGGAGAATCGCTTGGGCCTGGGAGGCGGAGGTTGCAGTGAGGTGAGA A G SNED1 Ensembl:ENSG00000162804 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs556458966 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265115 8328 RMVar_ID_8328 Human_SNP_ID_119207830 A-to-I Human chr2 + 241055104 241055104 241055104 GTGCCACTGAACTCCTACTTGGGTGATAGAGTAAGACTCTGTCTCAAAAAAAAAAAAGAAAAAAT GTGCCACTGAACTCCTACTTGGGTGATAGAGTGAGACTCTGTCTCAAAAAAAAAAAAGAAAAAAT A G SNED1 Ensembl:ENSG00000162804 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049537705 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265115 8329 RMVar_ID_8329 Human_SNP_ID_119208099 A-to-I Human chr2 + 241056390 241056390 241056390 CTCCTGCCTCTGCCTCCCAAGCTGCTGGGATTACAGGCATGAACCACTGTGCCCAGCTGAAATGA CTCCTGCCTCTGCCTCCCAAGCTGCTGGGATTGCAGGCATGAACCACTGTGCCCAGCTGAAATGA A G SNED1 Ensembl:ENSG00000162804 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs925111877 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265115 8330 RMVar_ID_8330 Human_SNP_ID_119208224 A-to-I Human chr2 + 241056772 241056771 241056773 CCGGCTAATTTTTTTTTATATTTAGTAGAGACAGGGTTTCACCGTGTTAGCCAGGATGGTCTCGA CCGGCTAATTTTTTTTTATATTTAGTAGAGAC__GGTTTCACCGTGTTAGCCAGGATGGTCTCGA CAG C SNED1 Ensembl:ENSG00000162804 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1248173298 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_265115 8331 RMVar_ID_8331 Human_SNP_ID_119223115 A-to-I Human chr2 + 241111333 241111333 241111333 CAGATATGGGCGGTGCAGCAGAGCACTGCAGCAGAGGGCCAGGAGGGTCCAAGCAGTGCTGTGAT CAGATATGGGCGGTGCAGCAGAGCACTGCAGCGGAGGGCCAGGAGGGTCCAAGCAGTGCTGTGAT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs2310875 Functional Loss SNV dbSNP153 33..33 33 - - - 8332 RMVar_ID_8332 Human_SNP_ID_119223116 A-to-I Human chr2 + 241111335 241111333 241111335 GATATGGGCGGTGCAGCAGAGCACTGCAGCAGAGGGCCAGGAGGGTCCAAGCAGTGCTGTGATCA GATATGGGCGGTGCAGCAGAGCACTGCAGCGGGGGGCCAGGAGGGTCCAAGCAGTGCTGTGATCA AGA GGG - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs796669999 Functional Loss MNV dbSNP153 31..33 33 - - - 8333 RMVar_ID_8333 Human_SNP_ID_119223116 A-to-I Human chr2 + 241111333 241111333 241111335 CAGATATGGGCGGTGCAGCAGAGCACTGCAGCAGAGGGCCAGGAGGGTCCAAGCAGTGCTGTGAT CAGATATGGGCGGTGCAGCAGAGCACTGCAGCGGGGGGCCAGGAGGGTCCAAGCAGTGCTGTGAT AGA GGG - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs796669999 Functional Loss MNV dbSNP153 33..35 33 - - - 8334 RMVar_ID_8334 Human_SNP_ID_119223118 A-to-I Human chr2 + 241111335 241111335 241111335 GATATGGGCGGTGCAGCAGAGCACTGCAGCAGAGGGCCAGGAGGGTCCAAGCAGTGCTGTGATCA GATATGGGCGGTGCAGCAGAGCACTGCAGCAGGGGGCCAGGAGGGTCCAAGCAGTGCTGTGATCA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs2310874 Functional Loss SNV dbSNP153 33..33 33 - - - 8335 RMVar_ID_8335 Human_SNP_ID_119257387 A-to-I Human chr2 + 241225297 241225296 241225297 CCTGTAATCCCAGGACTTTGGGAGGCTGAGGCAGGAGGATTACAAGGTCAGGAGTTCGGGACTAG CCTGTAATCCCAGGACTTTGGGAGGCTGAGGC_GGAGGATTACAAGGTCAGGAGTTCGGGACTAG CA C ANO7 Ensembl:ENSG00000146205 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs748834146 Functional Loss DEL dbSNP153 33..33 33 - - - 8336 RMVar_ID_8336 Human_SNP_ID_119257417 A-to-I Human chr2 + 241225404 241225404 241225404 AAATTATTCTGGGTGTGGTGGCGGGCATCTGTAATCCCAGCTATTTGGGAGGCTGAGGCAGGAGA AAATTATTCTGGGTGTGGTGGCGGGCATCTGTCATCCCAGCTATTTGGGAGGCTGAGGCAGGAGA A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978377301 Functional Loss SNV dbSNP153 33..33 33 - - - 8337 RMVar_ID_8337 Human_SNP_ID_119257418 A-to-I Human chr2 + 241225404 241225404 241225404 AAATTATTCTGGGTGTGGTGGCGGGCATCTGTAATCCCAGCTATTTGGGAGGCTGAGGCAGGAGA AAATTATTCTGGGTGTGGTGGCGGGCATCTGTGATCCCAGCTATTTGGGAGGCTGAGGCAGGAGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978377301 Functional Loss SNV dbSNP153 33..33 33 - - - 8338 RMVar_ID_8338 Human_SNP_ID_119259816 A-to-I Human chr2 + 241232693 241232693 241232693 CTCTTGGGCTGGGAGCGGTGGCTCACAGCTGTAGTCCCAGCTACTTGGGAGGTTGAGGCACGAGA CTCTTGGGCTGGGAGCGGTGGCTCACAGCTGTGGTCCCAGCTACTTGGGAGGTTGAGGCACGAGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202667835 Functional Loss SNV dbSNP153 33..33 33 - - - 8339 RMVar_ID_8339 Human_SNP_ID_119260741 A-to-I Human chr2 - 241235647 241235645 241235648 GTGTTTCGTGGAGCCCCATTGCTGAGCTTACAACGTCACTCTGCTCTCAGCTCCCACGGCCTAAC GTGTTTCGTGGAGCCCCATTGCTGAGCTTAC___GTCACTCTGCTCTCAGCTCCCACGGCCTAAC CGTT C HDLBP Ensembl:ENSG00000115677 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs775245937 Functional Loss DEL dbSNP153 32..34 33 - - - 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_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 8340 RMVar_ID_8340 Human_SNP_ID_119260741 A-to-I Human chr2 - 241235648 241235645 241235648 TGTGTTTCGTGGAGCCCCATTGCTGAGCTTACAACGTCACTCTGCTCTCAGCTCCCACGGCCTAA TGTGTTTCGTGGAGCCCCATTGCTGAGCTTAC___GTCACTCTGCTCTCAGCTCCCACGGCCTAA CGTT C HDLBP Ensembl:ENSG00000115677 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs775245937 Functional Loss DEL dbSNP153 33..35 33 - - - 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_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 8341 RMVar_ID_8341 Human_SNP_ID_119260745 A-to-I Human chr2 - 241235647 241235647 241235647 GTGTTTCGTGGAGCCCCATTGCTGAGCTTACAACGTCACTCTGCTCTCAGCTCCCACGGCCTAAC GTGTTTCGTGGAGCCCCATTGCTGAGCTTACATCGTCACTCTGCTCTCAGCTCCCACGGCCTAAC T A HDLBP Ensembl:ENSG00000115677 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170285345 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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 8342 RMVar_ID_8342 Human_SNP_ID_119260746 A-to-I Human chr2 - 241235648 241235648 241235648 TGTGTTTCGTGGAGCCCCATTGCTGAGCTTACAACGTCACTCTGCTCTCAGCTCCCACGGCCTAA TGTGTTTCGTGGAGCCCCATTGCTGAGCTTACGACGTCACTCTGCTCTCAGCTCCCACGGCCTAA T C HDLBP Ensembl:ENSG00000115677 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749177669 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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 8343 RMVar_ID_8343 Human_SNP_ID_119263858 A-to-I Human chr2 - 241245742 241245742 241245742 GCTGGAGTGCAGTGGTGCAGTCATGGCTCACTACAGCCTTGGCTTTCCAGACTCAAGCAGTCCTC GCTGGAGTGCAGTGGTGCAGTCATGGCTCACTGCAGCCTTGGCTTTCCAGACTCAAGCAGTCCTC T C HDLBP Ensembl:ENSG00000115677 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs769900042 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27180,RMVar_hsa_circ_208055,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_6493,RMVar_hsa_circ_60705,RMVar_hsa_circ_54737,RMVar_hsa_circ_113630,RMVar_hsa_circ_208068,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_63741,RMVar_hsa_circ_56554,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_372552,RMVar_hsa_circ_26458,RMVar_hsa_circ_56491,RMVar_hsa_circ_208083,RMVar_hsa_circ_208084 8344 RMVar_ID_8344 Human_SNP_ID_119265525 A-to-I Human chr2 - 241251772 241251767 241251773 TGGAATTTCACCATGTTGTCTAGGCTGGTGTCAAACTGCTGACCTTAGTTGATCTGCCCACCTCG TGGAATTTCACCATGTTGTCTAGGCTGGTGT______GCTGACCTTAGTTGATCTGCCCACCTCG CAGTTTG C HDLBP Ensembl:ENSG00000115677 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1412468567 Functional Loss DEL dbSNP153 32..37 33 - - - Human_RBP_ID_13821294 RMVar_hsa_circ_27180,RMVar_hsa_circ_208055,RMVar_hsa_circ_335674,RMVar_hsa_circ_118685,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_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_98169,RMVar_hsa_circ_208079,RMVar_hsa_circ_26458,RMVar_hsa_circ_56491,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_55423,RMVar_hsa_circ_115077,RMVar_hsa_circ_62964,RMVar_hsa_circ_208088,RMVar_hsa_circ_375899,RMVar_hsa_circ_208089 8345 RMVar_ID_8345 Human_SNP_ID_119265526 A-to-I Human chr2 - 241251772 241251772 241251772 TGGAATTTCACCATGTTGTCTAGGCTGGTGTCAAACTGCTGACCTTAGTTGATCTGCCCACCTCG TGGAATTTCACCATGTTGTCTAGGCTGGTGTCGAACTGCTGACCTTAGTTGATCTGCCCACCTCG T C HDLBP Ensembl:ENSG00000115677 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1312085002 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13821294 RMVar_hsa_circ_27180,RMVar_hsa_circ_208055,RMVar_hsa_circ_335674,RMVar_hsa_circ_118685,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_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_98169,RMVar_hsa_circ_208079,RMVar_hsa_circ_26458,RMVar_hsa_circ_56491,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_55423,RMVar_hsa_circ_115077,RMVar_hsa_circ_62964,RMVar_hsa_circ_208088,RMVar_hsa_circ_375899,RMVar_hsa_circ_208089 8346 RMVar_ID_8346 Human_SNP_ID_119265652 A-to-I Human chr2 - 241252285 241252285 241252285 GTTGGCCAGGCTTGTCTCAAATTCCTGGGCTCAGGTGATCTGCCCACCTTGGCCTCCCAAGGTGC GTTGGCCAGGCTTGTCTCAAATTCCTGGGCTCGGGTGATCTGCCCACCTTGGCCTCCCAAGGTGC T C HDLBP Ensembl:ENSG00000115677 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1413782059 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17570278 RMVar_hsa_circ_27180,RMVar_hsa_circ_208055,RMVar_hsa_circ_335674,RMVar_hsa_circ_118685,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_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_98169,RMVar_hsa_circ_208079,RMVar_hsa_circ_26458,RMVar_hsa_circ_56491,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_55423,RMVar_hsa_circ_115077,RMVar_hsa_circ_62964,RMVar_hsa_circ_208088,RMVar_hsa_circ_375899,RMVar_hsa_circ_208089 8347 RMVar_ID_8347 Human_SNP_ID_119265680 A-to-I Human chr2 - 241252415 241252415 241252415 TCACTACAACCTCTGCCTACCGGGCTCAAGCAATTCTCCAGCTTCAGCCTCCTGAGTAGCTGGGA TCACTACAACCTCTGCCTACCGGGCTCAAGCAGTTCTCCAGCTTCAGCCTCCTGAGTAGCTGGGA T C HDLBP Ensembl:ENSG00000115677 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs980111123 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27180,RMVar_hsa_circ_208055,RMVar_hsa_circ_335674,RMVar_hsa_circ_118685,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_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_98169,RMVar_hsa_circ_208079,RMVar_hsa_circ_26458,RMVar_hsa_circ_56491,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_55423,RMVar_hsa_circ_115077,RMVar_hsa_circ_62964,RMVar_hsa_circ_208088,RMVar_hsa_circ_375899,RMVar_hsa_circ_208089 8348 RMVar_ID_8348 Human_SNP_ID_119265681 A-to-I Human chr2 - 241252416 241252416 241252416 CTCACTACAACCTCTGCCTACCGGGCTCAAGCAATTCTCCAGCTTCAGCCTCCTGAGTAGCTGGG CTCACTACAACCTCTGCCTACCGGGCTCAAGCGATTCTCCAGCTTCAGCCTCCTGAGTAGCTGGG T C HDLBP Ensembl:ENSG00000115677 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs772069380 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27180,RMVar_hsa_circ_208055,RMVar_hsa_circ_335674,RMVar_hsa_circ_118685,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_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_98169,RMVar_hsa_circ_208079,RMVar_hsa_circ_26458,RMVar_hsa_circ_56491,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_55423,RMVar_hsa_circ_115077,RMVar_hsa_circ_62964,RMVar_hsa_circ_208088,RMVar_hsa_circ_375899,RMVar_hsa_circ_208089 8349 RMVar_ID_8349 Human_SNP_ID_119265687 A-to-I Human chr2 - 241252439 241252439 241252439 GGAGTGCAGTGGCGTGATCTCAGCTCACTACAACCTCTGCCTACCGGGCTCAAGCAATTCTCCAG GGAGTGCAGTGGCGTGATCTCAGCTCACTACAGCCTCTGCCTACCGGGCTCAAGCAATTCTCCAG T C HDLBP Ensembl:ENSG00000115677 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1192315374 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5196343 RMVar_hsa_circ_27180,RMVar_hsa_circ_208055,RMVar_hsa_circ_335674,RMVar_hsa_circ_118685,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_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_98169,RMVar_hsa_circ_208079,RMVar_hsa_circ_26458,RMVar_hsa_circ_56491,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_55423,RMVar_hsa_circ_115077,RMVar_hsa_circ_62964,RMVar_hsa_circ_208088,RMVar_hsa_circ_375899,RMVar_hsa_circ_208089 8350 RMVar_ID_8350 Human_SNP_ID_119266206 A-to-I Human chr2 - 241254250 241254250 241254250 ATTTTATTCCTTTTTTTTAGTGACAAAGCCTCACTCTGTCACCCAGGCTGGGGTGCAGTAGCGCA ATTTTATTCCTTTTTTTTAGTGACAAAGCCTCGCTCTGTCACCCAGGCTGGGGTGCAGTAGCGCA T C HDLBP Ensembl:ENSG00000115677 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1028942276 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27180,RMVar_hsa_circ_208055,RMVar_hsa_circ_335674,RMVar_hsa_circ_118685,RMVar_hsa_circ_208056,RMVar_hsa_circ_77777,RMVar_hsa_circ_208063,RMVar_hsa_circ_30135,RMVar_hsa_circ_6493,RMVar_hsa_circ_54737,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_55423,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 8351 RMVar_ID_8351 Human_SNP_ID_119268179 A-to-I Human chr2 - 241261011 241261011 241261011 TTTTGTTTGTTTTTTGGCAGATGCGGGTTTTCACCATGTTGCCCACTCTGGTCTCAAACCCCTAG TTTTGTTTGTTTTTTGGCAGATGCGGGTTTTCGCCATGTTGCCCACTCTGGTCTCAAACCCCTAG T C HDLBP Ensembl:ENSG00000115677 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1462834353 Functional Loss SNV dbSNP153 33..33 33 - - - 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_208072,RMVar_hsa_circ_89716,RMVar_hsa_circ_208078,RMVar_hsa_circ_353105,RMVar_hsa_circ_26458,RMVar_hsa_circ_19903,RMVar_hsa_circ_20061,RMVar_hsa_circ_208086,RMVar_hsa_circ_324760,RMVar_hsa_circ_359290,RMVar_hsa_circ_48205,RMVar_hsa_circ_62964,RMVar_hsa_circ_371246,RMVar_hsa_circ_208090,RMVar_hsa_circ_354695,RMVar_hsa_circ_59639,RMVar_hsa_circ_309108,RMVar_hsa_circ_359828,RMVar_hsa_circ_208091,RMVar_hsa_circ_92340,RMVar_hsa_circ_15630,RMVar_hsa_circ_208094,RMVar_hsa_circ_208096,RMVar_hsa_circ_102687 8352 RMVar_ID_8352 Human_SNP_ID_119268644 A-to-I Human chr2 - 241262725 241262725 241262725 CTGTCATGAAAGCTCGGAAGGACATTGTTGCTAGACTGCAGACTCAGGTGGGTAGCCTGAGGCCT CTGTCATGAAAGCTCGGAAGGACATTGTTGCTGGACTGCAGACTCAGGTGGGTAGCCTGAGGCCT T C HDLBP Ensembl:ENSG00000115677 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1473316822 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_916100,Human_RBP_ID_1584938,Human_RBP_ID_1913738,Human_RBP_ID_3620125,Human_RBP_ID_3959982,Human_RBP_ID_5194547,Human_RBP_ID_5589221,Human_RBP_ID_8515605,Human_RBP_ID_8847033,Human_RBP_ID_9104664,Human_RBP_ID_9385906,Human_RBP_ID_13821461,Human_RBP_ID_18757251,Human_RBP_ID_19001021,Human_RBP_ID_22076918,Human_RBP_ID_24546275,Human_RBP_ID_26338899 Human_Splice_Rec_381265,Human_Splice_Rec_381319,Human_Splice_Rec_381375,Human_Splice_Rec_381427,Human_Splice_Rec_381499,Human_Splice_Rec_381627,Human_Splice_Rec_381653,Human_Splice_Rec_381669,Human_Splice_Rec_381693 Human_miRNA_ID_2946864,Human_miRNA_ID_2946865 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_14643,RMVar_hsa_circ_6493,RMVar_hsa_circ_113630,RMVar_hsa_circ_208072,RMVar_hsa_circ_89716,RMVar_hsa_circ_208078,RMVar_hsa_circ_353105,RMVar_hsa_circ_26458,RMVar_hsa_circ_19903,RMVar_hsa_circ_20061,RMVar_hsa_circ_208086,RMVar_hsa_circ_324760,RMVar_hsa_circ_359290,RMVar_hsa_circ_48205,RMVar_hsa_circ_62964,RMVar_hsa_circ_371246,RMVar_hsa_circ_208090,RMVar_hsa_circ_354695,RMVar_hsa_circ_59639,RMVar_hsa_circ_309108,RMVar_hsa_circ_359828,RMVar_hsa_circ_208091,RMVar_hsa_circ_92340,RMVar_hsa_circ_15630,RMVar_hsa_circ_208094,RMVar_hsa_circ_208096,RMVar_hsa_circ_102687,RMVar_hsa_circ_50433,RMVar_hsa_circ_304573,RMVar_hsa_circ_208097 8353 RMVar_ID_8353 Human_SNP_ID_119275228 A-to-I Human chr2 - 241287619 241287619 241287619 CAGGAGTTCAACACCAACCTGGCCAATGTGGTAAAATCCTGTCTCTACAAAAAAATATACAAAAA CAGGAGTTCAACACCAACCTGGCCAATGTGGTGAAATCCTGTCTCTACAAAAAAATATACAAAAA T C HDLBP Ensembl:ENSG00000115677 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs907931968 Functional Loss SNV dbSNP153 33..33 33 - - - 8354 RMVar_ID_8354 Human_SNP_ID_119278458 A-to-I Human chr2 - 241299726 241299726 241299726 TGTTTTTAGTAGAGATAGGGTTTCACCGTGTTAGCCAGGATGATCTCGATCTCCTGACCTCGTGA TGTTTTTAGTAGAGATAGGGTTTCACCGTGTTTGCCAGGATGATCTCGATCTCCTGACCTCGTGA T A HDLBP Ensembl:ENSG00000115677 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1479120222 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25525326 8355 RMVar_ID_8355 Human_SNP_ID_119284113 A-to-I Human chr2 + 241318881 241318881 241318881 CACCACACCTGGCTAATTTTTGTATTTTTGGTAGAGACGGGGTTTCACCATGTTGGCCAGGATGG CACCACACCTGGCTAATTTTTGTATTTTTGGTGGAGACGGGGTTTCACCATGTTGGCCAGGATGG A G SEPTIN2 Ensembl:ENSG00000168385 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1218108610 Functional Loss SNV dbSNP153 33..33 33 - - - 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_29898 8356 RMVar_ID_8356 Human_SNP_ID_119284123 A-to-I Human chr2 + 241318898 241318898 241318898 TTTTGTATTTTTGGTAGAGACGGGGTTTCACCATGTTGGCCAGGATGGTCTCAATCTTTTGACCT TTTTGTATTTTTGGTAGAGACGGGGTTTCACCCTGTTGGCCAGGATGGTCTCAATCTTTTGACCT A C SEPTIN2 Ensembl:ENSG00000168385 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1261326445 Functional Loss SNV dbSNP153 33..33 33 - - - 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_29898 8357 RMVar_ID_8357 Human_SNP_ID_119284124 A-to-I Human chr2 + 241318898 241318898 241318898 TTTTGTATTTTTGGTAGAGACGGGGTTTCACCATGTTGGCCAGGATGGTCTCAATCTTTTGACCT TTTTGTATTTTTGGTAGAGACGGGGTTTCACCGTGTTGGCCAGGATGGTCTCAATCTTTTGACCT A G SEPTIN2 Ensembl:ENSG00000168385 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1261326445 Functional Loss SNV dbSNP153 33..33 33 - - - 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_29898 8358 RMVar_ID_8358 Human_SNP_ID_119284125 A-to-I Human chr2 + 241318898 241318898 241318898 TTTTGTATTTTTGGTAGAGACGGGGTTTCACCATGTTGGCCAGGATGGTCTCAATCTTTTGACCT TTTTGTATTTTTGGTAGAGACGGGGTTTCACCTTGTTGGCCAGGATGGTCTCAATCTTTTGACCT A T SEPTIN2 Ensembl:ENSG00000168385 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1261326445 Functional Loss SNV dbSNP153 33..33 33 - - - 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_29898 8359 RMVar_ID_8359 Human_SNP_ID_119284322 A-to-I Human chr2 + 241319613 241319613 241319613 ATTTAAGCAGTTTTCCTTTTTTTCTTTTTTTGAGACAGTCTCACTCTGTCACCCAGGCTGGAGTG ATTTAAGCAGTTTTCCTTTTTTTCTTTTTTTGTGACAGTCTCACTCTGTCACCCAGGCTGGAGTG A T SEPTIN2 Ensembl:ENSG00000168385 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1382577859 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6901095,Human_RBP_ID_13823096 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_29898 8360 RMVar_ID_8360 Human_SNP_ID_119284325 A-to-I Human chr2 + 241319623 241319619 241319623 TTTTCCTTTTTTTCTTTTTTTGAGACAGTCTCACTCTGTCACCCAGGCTGGAGTGCAGCAGCACC TTTTCCTTTTTTTCTTTTTTTGAGACAGT____CTCTGTCACCCAGGCTGGAGTGCAGCAGCACC TCTCA T SEPTIN2 Ensembl:ENSG00000168385 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1306206647 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_13823096 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_29898 8361 RMVar_ID_8361 Human_SNP_ID_119284327 A-to-I Human chr2 + 241319623 241319623 241319623 TTTTCCTTTTTTTCTTTTTTTGAGACAGTCTCACTCTGTCACCCAGGCTGGAGTGCAGCAGCACC TTTTCCTTTTTTTCTTTTTTTGAGACAGTCTCGCTCTGTCACCCAGGCTGGAGTGCAGCAGCACC A G SEPTIN2 Ensembl:ENSG00000168385 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1387830880 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13823096 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_29898 8362 RMVar_ID_8362 Human_SNP_ID_119285087 A-to-I Human chr2 + 241322394 241322394 241322394 TTGGGAGGCTGAGGCGGGCGGGTCATGAGGTCAGGAGATCGAGACCATCCTGGCTAACACAGTGA TTGGGAGGCTGAGGCGGGCGGGTCATGAGGTCTGGAGATCGAGACCATCCTGGCTAACACAGTGA A T SEPTIN2 Ensembl:ENSG00000168385 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1214352520 Functional Loss SNV dbSNP153 33..33 33 - - - 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_62796,RMVar_hsa_circ_349631,RMVar_hsa_circ_29898,RMVar_hsa_circ_329789,RMVar_hsa_circ_208104 8363 RMVar_ID_8363 Human_SNP_ID_119285383 A-to-I Human chr2 + 241323264 241323264 241323264 ATGATCTCGGCTCACTGCAACCTCCGCCTCCCAGGTTCAAGCGATTCTCCTGTCTCAGCCTTCTG ATGATCTCGGCTCACTGCAACCTCCGCCTCCCTGGTTCAAGCGATTCTCCTGTCTCAGCCTTCTG A T SEPTIN2 Ensembl:ENSG00000168385 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1376528215 Functional Loss SNV dbSNP153 33..33 33 - - - 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_62796,RMVar_hsa_circ_349631,RMVar_hsa_circ_29898,RMVar_hsa_circ_329789,RMVar_hsa_circ_208104 8364 RMVar_ID_8364 Human_SNP_ID_119285418 A-to-I Human chr2 + 241323370 241323370 241323370 ATCAGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGACCT ATCAGTATTTTTAGTAGAGACGGGGTTTCACCGTGTTGGCCAGGCTGGTCTTGAACTCCTGACCT A G SEPTIN2 Ensembl:ENSG00000168385 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1267999476 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13823314,Human_RBP_ID_25587399 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_62796,RMVar_hsa_circ_349631,RMVar_hsa_circ_29898,RMVar_hsa_circ_329789,RMVar_hsa_circ_208104 8365 RMVar_ID_8365 Human_SNP_ID_119285817 A-to-I Human chr2 + 241324457 241324457 241324457 GTCACCAGGCTGGAGTGCAGTGGCATGATCTCAGCTCACTGCAACTTCTGCCTCCCACGTTCAAG GTCACCAGGCTGGAGTGCAGTGGCATGATCTCGGCTCACTGCAACTTCTGCCTCCCACGTTCAAG A G SEPTIN2 Ensembl:ENSG00000168385 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1214597105 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_382044,Human_Splice_Rec_382204 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_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_208105 8366 RMVar_ID_8366 Human_SNP_ID_119285852 A-to-I Human chr2 + 241324533 241324533 241324533 GCTCAGCCTCCGGAGTAGCTGGGACTGCAGACACGTGCCACCACGCTGGCTAATTTTTTGGATTT GCTCAGCCTCCGGAGTAGCTGGGACTGCAGACGCGTGCCACCACGCTGGCTAATTTTTTGGATTT A G SEPTIN2 Ensembl:ENSG00000168385 Protein coding intron GSE38233;GSE100210;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,cerebellum - 24183664,29129909,30559470 RNA-Seq:(High) rs1463660030 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6901181,Human_RBP_ID_13823378,Human_RBP_ID_18757301 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_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_208105 8367 RMVar_ID_8367 Human_SNP_ID_119285873 A-to-I Human chr2 + 241324584 241324584 241324584 AATTTTTTGGATTTTAGTAAATTCGGGGTTTCACCGTGTTGGCCAGGATGGCCTTGATCTGTTGA AATTTTTTGGATTTTAGTAAATTCGGGGTTTCGCCGTGTTGGCCAGGATGGCCTTGATCTGTTGA A G SEPTIN2 Ensembl:ENSG00000168385 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1317178085 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4602527,Human_RBP_ID_13823386 Human_Splice_Rec_382205 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_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_208105 8368 RMVar_ID_8368 Human_SNP_ID_119287355 A-to-I Human chr2 + 241329396 241329396 241329396 GTGATCCGCCCGCCTCGGCCTCTCAAAGCGCTAGGATTAATATAAATCTTACACAGACATCTTCA GTGATCCGCCCGCCTCGGCCTCTCAAAGCGCTGGGATTAATATAAATCTTACACAGACATCTTCA A G SEPTIN2 Ensembl:ENSG00000168385 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1037624126 Functional Loss SNV dbSNP153 33..33 33 - - - 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_348204,RMVar_hsa_circ_310151,RMVar_hsa_circ_283685,RMVar_hsa_circ_326498,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 8369 RMVar_ID_8369 Human_SNP_ID_119288002 A-to-I Human chr2 + 241331489 241331489 241331489 TATGATTTTGGCAACCTCCACCTCCCAGGTTTAAGTGATTCTCGTTTCTCAGCCTCCCCAAGTAG TATGATTTTGGCAACCTCCACCTCCCAGGTTTCAGTGATTCTCGTTTCTCAGCCTCCCCAAGTAG A C SEPTIN2 Ensembl:ENSG00000168385 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1447165367 Functional Loss SNV dbSNP153 33..33 33 - - - 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_348204,RMVar_hsa_circ_310151,RMVar_hsa_circ_283685,RMVar_hsa_circ_326498,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 8370 RMVar_ID_8370 Human_SNP_ID_119288034 A-to-I Human chr2 + 241331619 241331619 241331619 TGTCATATTGGCCAGGCTGGTGTTAAACTCCTAGCCTGAAGTGATCCACCCTTCTCAGCCTCCCA TGTCATATTGGCCAGGCTGGTGTTAAACTCCTCGCCTGAAGTGATCCACCCTTCTCAGCCTCCCA A C SEPTIN2 Ensembl:ENSG00000168385 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs765067144 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17570282 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_348204,RMVar_hsa_circ_310151,RMVar_hsa_circ_283685,RMVar_hsa_circ_326498,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 8371 RMVar_ID_8371 Human_SNP_ID_119288035 A-to-I Human chr2 + 241331625 241331625 241331625 ATTGGCCAGGCTGGTGTTAAACTCCTAGCCTGAAGTGATCCACCCTTCTCAGCCTCCCAAAGTAC ATTGGCCAGGCTGGTGTTAAACTCCTAGCCTGGAGTGATCCACCCTTCTCAGCCTCCCAAAGTAC A G SEPTIN2 Ensembl:ENSG00000168385 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1033600228 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17570282 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_348204,RMVar_hsa_circ_310151,RMVar_hsa_circ_283685,RMVar_hsa_circ_326498,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 8372 RMVar_ID_8372 Human_SNP_ID_119293647 A-to-I Human chr2 + 241349102 241349102 241349102 CTATTTTTGGCCAGGCACTGTGGGTTACACTTATAGTCCCAGCACTTTAGGAGGCCAAGGTGGGA CTATTTTTGGCCAGGCACTGTGGGTTACACTTGTAGTCCCAGCACTTTAGGAGGCCAAGGTGGGA A G SEPTIN2 Ensembl:ENSG00000168385 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1372301592 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25525926 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 8373 RMVar_ID_8373 Human_SNP_ID_119308065 A-to-I Human chr2 + 241406516 241406516 241406516 TCACCCAGCCTGGAGTGCAGTGGTGTGATCTCAGCTCAGTGCAGCCTCTGCCTCCTGGGCTCCAC TCACCCAGCCTGGAGTGCAGTGGTGTGATCTCGGCTCAGTGCAGCCTCTGCCTCCTGGGCTCCAC A G FARP2 Ensembl:ENSG00000006607 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs55778485 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17570284 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_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_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 8374 RMVar_ID_8374 Human_SNP_ID_119308378 A-to-I Human chr2 + 241407296 241407296 241407296 CTGCCCAGGCTGGAGTGCAGTGGTGCAGTTGTAGCACACTGCAACCTCAGACTGCTGGCCTCAAG CTGCCCAGGCTGGAGTGCAGTGGTGCAGTTGTGGCACACTGCAACCTCAGACTGCTGGCCTCAAG A G FARP2 Ensembl:ENSG00000006607 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1414486901 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_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 8375 RMVar_ID_8375 Human_SNP_ID_119308385 A-to-I Human chr2 + 241407312 241407312 241407312 GCAGTGGTGCAGTTGTAGCACACTGCAACCTCAGACTGCTGGCCTCAAGCCATCCTTTCACCTCA GCAGTGGTGCAGTTGTAGCACACTGCAACCTCCGACTGCTGGCCTCAAGCCATCCTTTCACCTCA A C FARP2 Ensembl:ENSG00000006607 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs893241761 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_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 8376 RMVar_ID_8376 Human_SNP_ID_119316352 A-to-I Human chr2 + 241437926 241437926 241437926 TGACCTCATGATCTGCCCGCCTCGGCCTCCCAAAGTGCTGGGAATACAGGCATGAGCCACCACGC TGACCTCATGATCTGCCCGCCTCGGCCTCCCAGAGTGCTGGGAATACAGGCATGAGCCACCACGC A G FARP2 Ensembl:ENSG00000006607 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1057006069 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13459,RMVar_hsa_circ_358423,RMVar_hsa_circ_75502,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_338599 8377 RMVar_ID_8377 Human_SNP_ID_119316477 A-to-I Human chr2 + 241438434 241438434 241438434 TTTAAATTAGCCAGGTGTGGTGGCACTGAACTATAGTCCCAGCTACTTGGGAGGCTGAGGTATGA TTTAAATTAGCCAGGTGTGGTGGCACTGAACTGTAGTCCCAGCTACTTGGGAGGCTGAGGTATGA A G FARP2 Ensembl:ENSG00000006607 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs550376264 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13824951 RMVar_hsa_circ_13459,RMVar_hsa_circ_358423,RMVar_hsa_circ_75502,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_338599 8378 RMVar_ID_8378 Human_SNP_ID_119320021 A-to-I Human chr2 + 241451888 241451888 241451888 GCGATTCTCCTACCTCAGCCTCCCGAGTAGCTAGAATTACAGGCATGCACAACCACACCCGGCAA GCGATTCTCCTACCTCAGCCTCCCGAGTAGCTGGAATTACAGGCATGCACAACCACACCCGGCAA A G FARP2 Ensembl:ENSG00000006607 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs981485838 Functional Loss SNV dbSNP153 33..33 33 - - - 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 8379 RMVar_ID_8379 Human_SNP_ID_119332408 A-to-I Human chr2 - 241495569 241495569 241495569 GAACTGTGCTGACTTGGAAGGTGCCCTGTGCTATGTCGTGCCTGCAGGGACACGTCGGATCCCGT GAACTGTGCTGACTTGGAAGGTGCCCTGTGCTGTGTCGTGCCTGCAGGGACACGTCGGATCCCGT T C STK25 Ensembl:ENSG00000115694 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1321730808 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_547261,Human_RBP_ID_775313,Human_RBP_ID_922982,Human_RBP_ID_1585067,Human_RBP_ID_1913996,Human_RBP_ID_3620443,Human_RBP_ID_13825423,Human_RBP_ID_18757419,Human_RBP_ID_22074392,Human_RBP_ID_23862459,Human_RBP_ID_27009295,Human_RBP_ID_27288433 Human_miRNA_ID_1141492,Human_miRNA_ID_2491164 RMVar_hsa_circ_208173,RMVar_hsa_circ_92368 8380 RMVar_ID_8380 Human_SNP_ID_119334675 A-to-I Human chr2 - 241502572 241502572 241502572 ACCTCGCCCGGCTAATTTTTTTTGTATTCAGTAGAGATGGGGTTTTACCATGTTAGTCAGGCTGG ACCTCGCCCGGCTAATTTTTTTTGTATTCAGTTGAGATGGGGTTTTACCATGTTAGTCAGGCTGG T A STK25 Ensembl:ENSG00000115694 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs907262548 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13825530 RMVar_hsa_circ_108203,RMVar_hsa_circ_208177,RMVar_hsa_circ_100929,RMVar_hsa_circ_208179 8381 RMVar_ID_8381 Human_SNP_ID_119336398 A-to-I Human chr2 - 241508110 241508110 241508110 CTCGCAGTGGACTGACGCCGCAGGGGCGAGCTAGCCGGCTCCGCGCCTCTCCGCGGGATCCAGAC CTCGCAGTGGACTGACGCCGCAGGGGCGAGCTGGCCGGCTCCGCGCCTCTCCGCGGGATCCAGAC T C STK25 Ensembl:ENSG00000115694 Protein coding 5'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1431752499 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_547287,Human_RBP_ID_4631565,Human_RBP_ID_9388387 Human_Splice_Rec_382560,Human_Splice_Rec_382624,Human_Splice_Rec_382666,Human_Splice_Rec_382700,Human_Splice_Rec_382814,Human_Splice_Rec_382852,Human_Splice_Rec_382858,Human_Splice_Rec_382864,Human_Splice_Rec_382870,Human_Splice_Rec_382874 RMVar_hsa_circ_108203,RMVar_hsa_circ_208177,RMVar_hsa_circ_100929,RMVar_hsa_circ_208179 8382 RMVar_ID_8382 Human_SNP_ID_119391108 A-to-I Human chr2 + 241691062 241691062 241691062 AACTCCTGACCTCAGGTGAGTCCACCTGCCTCAGCCTCCCAAAGCGCTGGGATTACAGGCGTGAG AACTCCTGACCTCAGGTGAGTCCACCTGCCTCGGCCTCCCAAAGCGCTGGGATTACAGGCGTGAG A G ING5 Ensembl:ENSG00000168395 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917878363 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21730 8383 RMVar_ID_8383 Human_SNP_ID_119395080 A-to-I Human chr2 + 241703795 241703795 241703795 GCCTGGATAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTTGA GCCTGGATAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGGTCTTGA A G ING5 Ensembl:ENSG00000168395 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1348243584 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21730 8384 RMVar_ID_8384 Human_SNP_ID_119395104 A-to-I Human chr2 + 241703866 241703865 241703866 GACCTCAACTGATTTGCCTGTCTTGATCTCCCAAAGTGCTGGGATTACAGGTATGAGCCACCACG GACCTCAACTGATTTGCCTGTCTTGATCTCCC_AAGTGCTGGGATTACAGGTATGAGCCACCACG CA C ING5 Ensembl:ENSG00000168395 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1438055374 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_21730 8385 RMVar_ID_8385 Human_SNP_ID_119397801 A-to-I Human chr2 + 241712866 241712866 241712866 TGGGCAACCAAGTGAGTCCCCCATCTCTACAAAAAATAGAAAAAATTAGCTGAGGGTGGTGGTGT TGGGCAACCAAGTGAGTCCCCCATCTCTACAAGAAATAGAAAAAATTAGCTGAGGGTGGTGGTGT A G ING5 Ensembl:ENSG00000168395 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1488334264 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_208208,RMVar_hsa_circ_90128,RMVar_hsa_circ_301911,RMVar_hsa_circ_208209,RMVar_hsa_circ_79826,RMVar_hsa_circ_82708,RMVar_hsa_circ_208214,RMVar_hsa_circ_208216,RMVar_hsa_circ_208215,RMVar_hsa_circ_288883 8386 RMVar_ID_8386 Human_SNP_ID_119397826 A-to-I Human chr2 + 241712964 241712964 241712964 CTGGGAGGATCATGAGCCACGATCGCACCACTACATTCCAGCCTGGGCCACAGCATGAGACTCTG CTGGGAGGATCATGAGCCACGATCGCACCACTGCATTCCAGCCTGGGCCACAGCATGAGACTCTG A G ING5 Ensembl:ENSG00000168395 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005096417 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_208208,RMVar_hsa_circ_90128,RMVar_hsa_circ_301911,RMVar_hsa_circ_208209,RMVar_hsa_circ_79826,RMVar_hsa_circ_82708,RMVar_hsa_circ_208214,RMVar_hsa_circ_208216,RMVar_hsa_circ_208215,RMVar_hsa_circ_288883 8387 RMVar_ID_8387 Human_SNP_ID_119398144 A-to-I Human chr2 + 241713869 241713869 241713869 AATACTTAGCTGAGTAGTTGGCAGCTGCCTGTAATCCCAGCTACTCGGGAGGCTGACGCAGGGAG AATACTTAGCTGAGTAGTTGGCAGCTGCCTGTGATCCCAGCTACTCGGGAGGCTGACGCAGGGAG A G ING5 Ensembl:ENSG00000168395 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1287579930 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_208208,RMVar_hsa_circ_90128,RMVar_hsa_circ_301911,RMVar_hsa_circ_208209,RMVar_hsa_circ_79826,RMVar_hsa_circ_82708,RMVar_hsa_circ_208214,RMVar_hsa_circ_208216,RMVar_hsa_circ_208215,RMVar_hsa_circ_288883 8388 RMVar_ID_8388 Human_SNP_ID_119408565 A-to-I Human chr2 + 241748238 241748238 241748238 CCGCCTCCTGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCGCCCA CCGCCTCCTGGTTCAAGCGATTCTCCTGCCTCCGCCTCCCAAGTAGCTGGGATTACAGGCGCCCA A C D2HGDH Ensembl:ENSG00000180902 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909738009 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124954,RMVar_hsa_circ_208218,RMVar_hsa_circ_16542,RMVar_hsa_circ_79788,RMVar_hsa_circ_348194,RMVar_hsa_circ_282654,RMVar_hsa_circ_208220,RMVar_hsa_circ_92053,RMVar_hsa_circ_116402,RMVar_hsa_circ_208221,RMVar_hsa_circ_208222 8389 RMVar_ID_8389 Human_SNP_ID_544383411 A-to-I Human chr13 - 106492049 106492049 106492049 GGAACAAAGACGGGTATTGTTGGGAAAGGAACAGGCTTGGAGGGAAGGGAGAAAGTAGGCCGCTG GGAACAAAGACGGGTATTGTTGGGAAAGGAACTGGCTTGGAGGGAAGGGAGAAAGTAGGCCGCTG T A EFNB2 Ensembl:ENSG00000125266 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs995711042 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3422987,Human_RBP_ID_4277291,Human_RBP_ID_6255411,Human_RBP_ID_8788081 8390 RMVar_ID_8390 Human_SNP_ID_544628336 A-to-I Human chr13 - 107455177 107455177 107455177 GGCTGGGGAGGCCTCAGAAAACTTACAATCATAGTGGAAGGGGAAGCAGGCACCATCTTACATGG GGCTGGGGAGGCCTCAGAAAACTTACAATCATTGTGGAAGGGGAAGCAGGCACCATCTTACATGG T A FAM155A Ensembl:ENSG00000204442 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1470624702 Functional Loss SNV dbSNP153 33..33 33 - - - 8391 RMVar_ID_8391 Human_SNP_ID_544641505 A-to-I Human chr13 - 107509971 107509971 107509971 CCTCTCCATCTCTATGAAGTACATGAAAAATTAGCTGGGCATGGTGGCGCATACCTGTGGTCCTA CCTCTCCATCTCTATGAAGTACATGAAAAATTGGCTGGGCATGGTGGCGCATACCTGTGGTCCTA T C FAM155A Ensembl:ENSG00000204442 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs753375471 Functional Loss SNV dbSNP153 33..33 33 - - - 8392 RMVar_ID_8392 Human_SNP_ID_544656075 A-to-I Human chr13 - 107568201 107568201 107568201 CAAGGTGGGAGGATTCCTTGAGCCCAGGAGCTAGAGACCAGCCTGGGCACCATGGTGAGACTCCA CAAGGTGGGAGGATTCCTTGAGCCCAGGAGCTGGAGACCAGCCTGGGCACCATGGTGAGACTCCA T C FAM155A Ensembl:ENSG00000204442 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1320052999 Functional Loss SNV dbSNP153 33..33 33 - - - 8393 RMVar_ID_8393 Human_SNP_ID_544679189 A-to-I Human chr13 - 107660167 107660167 107660167 CCAAAGTGCTGGGATTATAAGTGTGAGCCACCACACCCAACCTAAGATTTTTATAAATCACGTGA CCAAAGTGCTGGGATTATAAGTGTGAGCCACCGCACCCAACCTAAGATTTTTATAAATCACGTGA T C FAM155A Ensembl:ENSG00000204442 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs916254334 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_164636 8394 RMVar_ID_8394 Human_SNP_ID_544689624 A-to-I Human chr13 - 107701202 107701202 107701202 AGGTTGTTTCCATATTTTGGCTCTTGGGAATAATGCTGCAATGCACATGAGAGTGAAGGATGTCT AGGTTGTTTCCATATTTTGGCTCTTGGGAATAGTGCTGCAATGCACATGAGAGTGAAGGATGTCT T C FAM155A Ensembl:ENSG00000204442 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1414369925 Functional Loss SNV dbSNP153 33..33 33 - - - 8395 RMVar_ID_8395 Human_SNP_ID_544691622 A-to-I Human chr13 - 107708785 107708785 107708785 GTGCTGCAAACCACCATGGCACACGTTTACCTATGTAACAAACTTGCACATCCTGCACATGTACC GTGCTGCAAACCACCATGGCACACGTTTACCTGTGTAACAAACTTGCACATCCTGCACATGTACC T C FAM155A Ensembl:ENSG00000204442 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1453187172 Functional Loss SNV dbSNP153 33..33 33 - - - 8396 RMVar_ID_8396 Human_SNP_ID_544693125 A-to-I Human chr13 - 107714545 107714545 107714545 GGCTCACTGCAACCTCCCAAGTAGCTGGGACTACAGGCATGCACCACCATACCTGGCTAGCGTTT GGCTCACTGCAACCTCCCAAGTAGCTGGGACTGCAGGCATGCACCACCATACCTGGCTAGCGTTT T C FAM155A Ensembl:ENSG00000204442 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971630324 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_164638 8397 RMVar_ID_8397 Human_SNP_ID_544695765 A-to-I Human chr13 - 107724686 107724686 107724686 ATGGTGGTGCATGTCTGTAGTCCCAGCTATTCAGGAGGCTGAGGTGGAAGGATCGCTTGAGCCTG ATGGTGGTGCATGTCTGTAGTCCCAGCTATTCTGGAGGCTGAGGTGGAAGGATCGCTTGAGCCTG T A FAM155A Ensembl:ENSG00000204442 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1209923922 Functional Loss SNV dbSNP153 33..33 33 - - - 8398 RMVar_ID_8398 Human_SNP_ID_544695766 A-to-I Human chr13 - 107724686 107724686 107724686 ATGGTGGTGCATGTCTGTAGTCCCAGCTATTCAGGAGGCTGAGGTGGAAGGATCGCTTGAGCCTG ATGGTGGTGCATGTCTGTAGTCCCAGCTATTCGGGAGGCTGAGGTGGAAGGATCGCTTGAGCCTG T C FAM155A Ensembl:ENSG00000204442 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1209923922 Functional Loss SNV dbSNP153 33..33 33 - - - 8399 RMVar_ID_8399 Human_SNP_ID_544696805 A-to-I Human chr13 - 107728490 107728490 107728490 CCGGTGTGTGGTGTTCCCCTCCCTGTGTCCACATGTTCTCATTGTTCAACTCCCACGTATGAGTG CCGGTGTGTGGTGTTCCCCTCCCTGTGTCCACGTGTTCTCATTGTTCAACTCCCACGTATGAGTG T C FAM155A Ensembl:ENSG00000204442 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs941701125 Functional Loss SNV dbSNP153 33..33 33 - - - 8400 RMVar_ID_8400 Human_SNP_ID_544696836 A-to-I Human chr13 - 107728575 107728575 107728575 CTGTCATCCAGGTTTTAAGCCCCGCATGCATTAGGTATTTGTCCTAATGCTGTCCCTCCCCTTTC CTGTCATCCAGGTTTTAAGCCCCGCATGCATTCGGTATTTGTCCTAATGCTGTCCCTCCCCTTTC T G FAM155A Ensembl:ENSG00000204442 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1306958173 Functional Loss SNV dbSNP153 33..33 33 - - - 8401 RMVar_ID_8401 Human_SNP_ID_544697566 A-to-I Human chr13 - 107731570 107731570 107731570 CACATAGAGGGGACTAACACACAGTGGGACCTACTTGAGGGTCGGGGGTGCATGGGAGGGAGAGC CACATAGAGGGGACTAACACACAGTGGGACCTGCTTGAGGGTCGGGGGTGCATGGGAGGGAGAGC T C FAM155A Ensembl:ENSG00000204442 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs563768309 Functional Loss SNV dbSNP153 33..33 33 - - - 8402 RMVar_ID_8402 Human_SNP_ID_544704517 A-to-I Human chr13 - 107759403 107759403 107759403 GAGATGGAGACCATCCTGGCTAACATGGTGAAACCCCGCCTCTACTAAAAATACTAAAAATTATC GAGATGGAGACCATCCTGGCTAACATGGTGAACCCCCGCCTCTACTAAAAATACTAAAAATTATC T G FAM155A Ensembl:ENSG00000204442 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs929565279 Functional Loss SNV dbSNP153 33..33 33 - - - 8403 RMVar_ID_8403 Human_SNP_ID_544724574 A-to-I Human chr13 - 107837337 107837337 107837337 ATAGGCTCTGGAGGGGATGCCCAAGCATAATAACATCTGAGATGCACTGCTATGCATTCCTTTTC ATAGGCTCTGGAGGGGATGCCCAAGCATAATATCATCTGAGATGCACTGCTATGCATTCCTTTTC T A FAM155A Ensembl:ENSG00000204442 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1463930220 Functional Loss SNV dbSNP153 33..33 33 - - - 8404 RMVar_ID_8404 Human_SNP_ID_544724577 A-to-I Human chr13 - 107837340 107837340 107837340 TCAATAGGCTCTGGAGGGGATGCCCAAGCATAATAACATCTGAGATGCACTGCTATGCATTCCTT TCAATAGGCTCTGGAGGGGATGCCCAAGCATAGTAACATCTGAGATGCACTGCTATGCATTCCTT T C FAM155A Ensembl:ENSG00000204442 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1020389088 Functional Loss SNV dbSNP153 33..33 33 - - - 8405 RMVar_ID_8405 Human_SNP_ID_544724832 A-to-I Human chr13 - 107838273 107838273 107838273 GGGACCCTGCTGAACTGTAGACTCTGATTCATAGGATGGAGTTGGGTCTGAGGGTGCTTTTCTGA GGGACCCTGCTGAACTGTAGACTCTGATTCATTGGATGGAGTTGGGTCTGAGGGTGCTTTTCTGA T A FAM155A Ensembl:ENSG00000204442 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs181659678 Functional Loss SNV dbSNP153 33..33 33 - - - 8406 RMVar_ID_8406 Human_SNP_ID_544724833 A-to-I Human chr13 - 107838273 107838273 107838273 GGGACCCTGCTGAACTGTAGACTCTGATTCATAGGATGGAGTTGGGTCTGAGGGTGCTTTTCTGA GGGACCCTGCTGAACTGTAGACTCTGATTCATCGGATGGAGTTGGGTCTGAGGGTGCTTTTCTGA T G FAM155A Ensembl:ENSG00000204442 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs181659678 Functional Loss SNV dbSNP153 33..33 33 - - - 8407 RMVar_ID_8407 Human_SNP_ID_544724840 A-to-I Human chr13 - 107838292 107838292 107838292 TGTTTTTGAGCATCCCCTTGGGACCCTGCTGAACTGTAGACTCTGATTCATAGGATGGAGTTGGG TGTTTTTGAGCATCCCCTTGGGACCCTGCTGATCTGTAGACTCTGATTCATAGGATGGAGTTGGG T A FAM155A Ensembl:ENSG00000204442 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1566501872 Functional Loss SNV dbSNP153 33..33 33 - - - 8408 RMVar_ID_8408 Human_SNP_ID_544724852 A-to-I Human chr13 - 107838374 107838369 107838375 AAAGGAAAAATCAAAACACTCAATTTGATTTTAATTTATTCTTAAGGAAAAGGAATGCATAGCGG AAAGGAAAAATCAAAACACTCAATTTGATTT______ATTCTTAAGGAAAAGGAATGCATAGCGG TAAATTA T FAM155A Ensembl:ENSG00000204442 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1224704888 Functional Loss DEL dbSNP153 32..37 33 - - - 8409 RMVar_ID_8409 Human_SNP_ID_544724853 A-to-I Human chr13 - 107838374 107838374 107838374 AAAGGAAAAATCAAAACACTCAATTTGATTTTAATTTATTCTTAAGGAAAAGGAATGCATAGCGG AAAGGAAAAATCAAAACACTCAATTTGATTTTTATTTATTCTTAAGGAAAAGGAATGCATAGCGG T A FAM155A Ensembl:ENSG00000204442 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs764937977 Functional Loss SNV dbSNP153 33..33 33 - - - 8410 RMVar_ID_8410 Human_SNP_ID_544724854 A-to-I Human chr13 - 107838374 107838374 107838374 AAAGGAAAAATCAAAACACTCAATTTGATTTTAATTTATTCTTAAGGAAAAGGAATGCATAGCGG AAAGGAAAAATCAAAACACTCAATTTGATTTTCATTTATTCTTAAGGAAAAGGAATGCATAGCGG T G FAM155A Ensembl:ENSG00000204442 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs764937977 Functional Loss SNV dbSNP153 33..33 33 - - - 8411 RMVar_ID_8411 Human_SNP_ID_544724858 A-to-I Human chr13 - 107838398 107838398 107838398 CAGGAAAAAGAATACTGCAACTGAAAAGGAAAAATCAAAACACTCAATTTGATTTTAATTTATTC CAGGAAAAAGAATACTGCAACTGAAAAGGAAACATCAAAACACTCAATTTGATTTTAATTTATTC T G FAM155A Ensembl:ENSG00000204442 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs940011915 Functional Loss SNV dbSNP153 33..33 33 - - - 8412 RMVar_ID_8412 Human_SNP_ID_544728056 A-to-I Human chr13 - 107851941 107851941 107851941 ATAGCCGGGCATGGTGGCATGCACTGAGTCCAAGCTACATGGGGGACTGAGGTAGGAGGGTTGCT ATAGCCGGGCATGGTGGCATGCACTGAGTCCAGGCTACATGGGGGACTGAGGTAGGAGGGTTGCT T C FAM155A Ensembl:ENSG00000204442 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs897254572 Functional Loss SNV dbSNP153 33..33 33 - - - 8413 RMVar_ID_8413 Human_SNP_ID_544728059 A-to-I Human chr13 - 107851955 107851955 107851955 AATTAAAAAAAAAAATAGCCGGGCATGGTGGCATGCACTGAGTCCAAGCTACATGGGGGACTGAG AATTAAAAAAAAAAATAGCCGGGCATGGTGGCGTGCACTGAGTCCAAGCTACATGGGGGACTGAG T C FAM155A Ensembl:ENSG00000204442 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1221528792 Functional Loss SNV dbSNP153 33..33 33 - - - 8414 RMVar_ID_8414 Human_SNP_ID_544729128 A-to-I Human chr13 - 107856153 107856153 107856153 CCTGTAATCCCAGCACTTTGGGAGGCTAAGACAGGAGGATCGCTTGAGTTCAGGAGTTTGAGATC CCTGTAATCCCAGCACTTTGGGAGGCTAAGACGGGAGGATCGCTTGAGTTCAGGAGTTTGAGATC T C FAM155A Ensembl:ENSG00000204442 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1193674628 Functional Loss SNV dbSNP153 33..33 33 - - - 8415 RMVar_ID_8415 Human_SNP_ID_544733703 A-to-I Human chr13 - 107873512 107873512 107873512 TAGAGACAGGGTTTCACTATGTTGGCGAGGCTAGTCTTGAACTCCTTGCCTCATGTGATCCACCC TAGAGACAGGGTTTCACTATGTTGGCGAGGCTGGTCTTGAACTCCTTGCCTCATGTGATCCACCC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs753960151 Functional Loss SNV dbSNP153 33..33 33 - - - 8416 RMVar_ID_8416 Human_SNP_ID_545071690 A-to-I Human chr13 - 109217743 109217743 109217743 CACATAAAGGGCAGTTTATTAAGTATTAACCTACACGATCACAAGGTCCCACAATAGTCCATCTG CACATAAAGGGCAGTTTATTAAGTATTAACCTGCACGATCACAAGGTCCCACAATAGTCCATCTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1217958666 Functional Loss SNV dbSNP153 33..33 33 - - - 8417 RMVar_ID_8417 Human_SNP_ID_545072980 A-to-I Human chr13 - 109219000 109218996 109219000 GACTGGCTCTCCTTGCTCCTCAGCCTGCAGACAGACTATTGTGGGACCTTGTGATTGTGTAGGTT GACTGGCTCTCCTTGCTCCTCAGCCTGCAGAC____TATTGTGGGACCTTGTGATTGTGTAGGTT AGTCT A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1411147758 Functional Loss DEL dbSNP153 33..36 33 - - - 8418 RMVar_ID_8418 Human_SNP_ID_545072981 A-to-I Human chr13 - 109219000 109219000 109219000 GACTGGCTCTCCTTGCTCCTCAGCCTGCAGACAGACTATTGTGGGACCTTGTGATTGTGTAGGTT GACTGGCTCTCCTTGCTCCTCAGCCTGCAGACGGACTATTGTGGGACCTTGTGATTGTGTAGGTT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs930359260 Functional Loss SNV dbSNP153 33..33 33 - - - 8419 RMVar_ID_8419 Human_SNP_ID_545073028 A-to-I Human chr13 - 109219094 109219094 109219094 GACTAACTTAGCCTCCCAGCTTACATCTTTCTACCTCGCTGGAAGCTTCCTGCCCTCGAACATTG GACTAACTTAGCCTCCCAGCTTACATCTTTCTGCCTCGCTGGAAGCTTCCTGCCCTCGAACATTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1231530564 Functional Loss SNV dbSNP153 33..33 33 - - - 8420 RMVar_ID_8420 Human_SNP_ID_545073047 A-to-I Human chr13 - 109219180 109219180 109219180 AGACCCACCCTTAAGGTGGGTGGGCAAAATCTAATCAGCTGCCAGTGCAGCTAGAATATAAGCAG AGACCCACCCTTAAGGTGGGTGGGCAAAATCTGATCAGCTGCCAGTGCAGCTAGAATATAAGCAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs778127408 Functional Loss SNV dbSNP153 33..33 33 - - - 8421 RMVar_ID_8421 Human_SNP_ID_545083553 A-to-I Human chr13 - 109263091 109263091 109263091 CTCAAGTGATCCGCCTGCCTTGGCCTCCCAAAATGCTGCGATTACAGGCATGAACCACTAAGCCC CTCAAGTGATCCGCCTGCCTTGGCCTCCCAAATTGCTGCGATTACAGGCATGAACCACTAAGCCC T A lnc-IRS2-8 RNACentral:URS00008BA0D0 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1299771988 Functional Loss SNV dbSNP153 33..33 33 - - - 8422 RMVar_ID_8422 Human_SNP_ID_545083661 A-to-I Human chr13 - 109263471 109263471 109263471 CTGTAATTCCCGTTACTAGGGAGGCTGAGGCAAGAGAATCGCTTGGACCAGGAAGGCAGAGGTTG CTGTAATTCCCGTTACTAGGGAGGCTGAGGCAGGAGAATCGCTTGGACCAGGAAGGCAGAGGTTG T C lnc-IRS2-8 RNACentral:URS00008BA0D0 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053881921 Functional Loss SNV dbSNP153 33..33 33 - - - 8423 RMVar_ID_8423 Human_SNP_ID_545219391 A-to-I Human chr13 - 109775960 109775960 109775960 TATTTTTAGTAGAGATGGGATTTCACCGTGTTAGCCAGGCTGGTCTCGATCTCCTGACCCCGTGA TATTTTTAGTAGAGATGGGATTTCACCGTGTTTGCCAGGCTGGTCTCGATCTCCTGACCCCGTGA T A IRS2 Ensembl:ENSG00000185950 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1566409985 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114879,RMVar_hsa_circ_164695 8424 RMVar_ID_8424 Human_SNP_ID_545315630 A-to-I Human chr13 - 110149579 110149579 110149579 GTCCTTTAACATAGGTTTTTAAAGACTAGGATATTGAATGTGAAACATCCGTTTTCATTGTTCAC GTCCTTTAACATAGGTTTTTAAAGACTAGGATGTTGAATGTGAAACATCCGTTTTCATTGTTCAC T C COL4A1 Ensembl:ENSG00000187498 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1339269000 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_431955,Human_RBP_ID_4277409,Human_RBP_ID_18266387,Human_RBP_ID_23584721 8425 RMVar_ID_8425 Human_SNP_ID_545382823 A-to-I Human chr13 + 110398735 110398724 110398736 AAGAAAAAGAAAGAAAGAAAGGGAAAGAAAGGAAGAAAGAATCAAATAACAAAAAGCACAGTCAG AAGAAAAAGAAAGAAAGAAAGG____________GAAAGAATCAAATAACAAAAAGCACAGTCAG GGAAAGAAAGGAA G COL4A2 Ensembl:ENSG00000134871 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1425834822 Functional Loss DEL dbSNP153 23..34 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 8426 RMVar_ID_8426 Human_SNP_ID_545412298 A-to-I Human chr13 + 110505087 110505087 110505087 AAATTAAACATAGGGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAG AAATTAAACATAGGGGCCGGGCGCGGTGGCTCTCGCCTGTAATCCCAGCACTTTGGGAGGCTGAG A T COL4A2 Ensembl:ENSG00000134871 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1262617797 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_118066 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 8427 RMVar_ID_8427 Human_SNP_ID_545462691 A-to-I Human chr13 - 110684522 110684522 110684522 GCAAACAAAGCCGGGTGACATTTCAACAGAAAACCCTGCCCTGTCCCTTCAGCGTCCTCCCTGGT GCAAACAAAGCCGGGTGACATTTCAACAGAAAGCCCTGCCCTGTCCCTTCAGCGTCCTCCCTGGT T C CARS2 Ensembl:ENSG00000134905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs926186938 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114303,RMVar_hsa_circ_164754,RMVar_hsa_circ_76335,RMVar_hsa_circ_164753,RMVar_hsa_circ_36728,RMVar_hsa_circ_40801,RMVar_hsa_circ_63373,RMVar_hsa_circ_367471,RMVar_hsa_circ_61249,RMVar_hsa_circ_58452,RMVar_hsa_circ_295262,RMVar_hsa_circ_312643,RMVar_hsa_circ_164760,RMVar_hsa_circ_164761,RMVar_hsa_circ_327531,RMVar_hsa_circ_109154,RMVar_hsa_circ_164765,RMVar_hsa_circ_164763,RMVar_hsa_circ_325567,RMVar_hsa_circ_326199,RMVar_hsa_circ_164764,RMVar_hsa_circ_301088,RMVar_hsa_circ_295564,RMVar_hsa_circ_347313 8428 RMVar_ID_8428 Human_SNP_ID_545462692 A-to-I Human chr13 - 110684522 110684522 110684522 GCAAACAAAGCCGGGTGACATTTCAACAGAAAACCCTGCCCTGTCCCTTCAGCGTCCTCCCTGGT GCAAACAAAGCCGGGTGACATTTCAACAGAAACCCCTGCCCTGTCCCTTCAGCGTCCTCCCTGGT T G CARS2 Ensembl:ENSG00000134905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs926186938 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114303,RMVar_hsa_circ_164754,RMVar_hsa_circ_76335,RMVar_hsa_circ_164753,RMVar_hsa_circ_36728,RMVar_hsa_circ_40801,RMVar_hsa_circ_63373,RMVar_hsa_circ_367471,RMVar_hsa_circ_61249,RMVar_hsa_circ_58452,RMVar_hsa_circ_295262,RMVar_hsa_circ_312643,RMVar_hsa_circ_164760,RMVar_hsa_circ_164761,RMVar_hsa_circ_327531,RMVar_hsa_circ_109154,RMVar_hsa_circ_164765,RMVar_hsa_circ_164763,RMVar_hsa_circ_325567,RMVar_hsa_circ_326199,RMVar_hsa_circ_164764,RMVar_hsa_circ_301088,RMVar_hsa_circ_295564,RMVar_hsa_circ_347313 8429 RMVar_ID_8429 Human_SNP_ID_545462905 A-to-I Human chr13 - 110685430 110685428 110685430 TTCCTGTCCTTCCTGGGTCCTACTTGGAGCGTAAGATGAGCACGTGAGGCCCTGAGGATCTGCTC TTCCTGTCCTTCCTGGGTCCTACTTGGAGCGT__GATGAGCACGTGAGGCCCTGAGGATCTGCTC CTT C CARS2 Ensembl:ENSG00000134905 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1405996312 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_114303,RMVar_hsa_circ_164754,RMVar_hsa_circ_76335,RMVar_hsa_circ_164753,RMVar_hsa_circ_36728,RMVar_hsa_circ_40801,RMVar_hsa_circ_63373,RMVar_hsa_circ_367471,RMVar_hsa_circ_61249,RMVar_hsa_circ_58452,RMVar_hsa_circ_295262,RMVar_hsa_circ_312643,RMVar_hsa_circ_164760,RMVar_hsa_circ_164761,RMVar_hsa_circ_327531,RMVar_hsa_circ_109154,RMVar_hsa_circ_164765,RMVar_hsa_circ_164763,RMVar_hsa_circ_325567,RMVar_hsa_circ_326199,RMVar_hsa_circ_164764,RMVar_hsa_circ_301088,RMVar_hsa_circ_295564,RMVar_hsa_circ_347313 8430 RMVar_ID_8430 Human_SNP_ID_545462906 A-to-I Human chr13 - 110685430 110685430 110685430 TTCCTGTCCTTCCTGGGTCCTACTTGGAGCGTAAGATGAGCACGTGAGGCCCTGAGGATCTGCTC TTCCTGTCCTTCCTGGGTCCTACTTGGAGCGTGAGATGAGCACGTGAGGCCCTGAGGATCTGCTC T C CARS2 Ensembl:ENSG00000134905 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4773237 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_642,GWAS_ID_643,GWAS_ID_644,GWAS_ID_645,GWAS_ID_646,GWAS_ID_647,GWAS_ID_648,GWAS_ID_649,GWAS_ID_650 RMVar_hsa_circ_114303,RMVar_hsa_circ_164754,RMVar_hsa_circ_76335,RMVar_hsa_circ_164753,RMVar_hsa_circ_36728,RMVar_hsa_circ_40801,RMVar_hsa_circ_63373,RMVar_hsa_circ_367471,RMVar_hsa_circ_61249,RMVar_hsa_circ_58452,RMVar_hsa_circ_295262,RMVar_hsa_circ_312643,RMVar_hsa_circ_164760,RMVar_hsa_circ_164761,RMVar_hsa_circ_327531,RMVar_hsa_circ_109154,RMVar_hsa_circ_164765,RMVar_hsa_circ_164763,RMVar_hsa_circ_325567,RMVar_hsa_circ_326199,RMVar_hsa_circ_164764,RMVar_hsa_circ_301088,RMVar_hsa_circ_295564,RMVar_hsa_circ_347313 8431 RMVar_ID_8431 Human_SNP_ID_545463389 A-to-I Human chr13 - 110687505 110687505 110687505 CCCGGCTACATTTTTTTTGTTTTGGTATTTTTAGTAGAGATAAGGTTTCACCATGTTGGCCAAGC CCCGGCTACATTTTTTTTGTTTTGGTATTTTTGGTAGAGATAAGGTTTCACCATGTTGGCCAAGC T C CARS2 Ensembl:ENSG00000134905 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1187948638 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114303,RMVar_hsa_circ_164754,RMVar_hsa_circ_76335,RMVar_hsa_circ_164753,RMVar_hsa_circ_36728,RMVar_hsa_circ_40801,RMVar_hsa_circ_63373,RMVar_hsa_circ_367471,RMVar_hsa_circ_61249,RMVar_hsa_circ_58452,RMVar_hsa_circ_295262,RMVar_hsa_circ_312643,RMVar_hsa_circ_164760,RMVar_hsa_circ_164761,RMVar_hsa_circ_327531,RMVar_hsa_circ_109154,RMVar_hsa_circ_164765,RMVar_hsa_circ_164763,RMVar_hsa_circ_325567,RMVar_hsa_circ_326199,RMVar_hsa_circ_164764,RMVar_hsa_circ_301088,RMVar_hsa_circ_295564,RMVar_hsa_circ_347313 8432 RMVar_ID_8432 Human_SNP_ID_545463411 A-to-I Human chr13 - 110687579 110687579 110687579 TGCCTCCCTGGTTCAAGCGATTCTCCCGTCTCAGCCTCCTGAATAGCTGGGACTACAAGGTGCGT TGCCTCCCTGGTTCAAGCGATTCTCCCGTCTCGGCCTCCTGAATAGCTGGGACTACAAGGTGCGT T C CARS2 Ensembl:ENSG00000134905 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1358894327 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114303,RMVar_hsa_circ_164754,RMVar_hsa_circ_76335,RMVar_hsa_circ_164753,RMVar_hsa_circ_36728,RMVar_hsa_circ_40801,RMVar_hsa_circ_63373,RMVar_hsa_circ_367471,RMVar_hsa_circ_61249,RMVar_hsa_circ_58452,RMVar_hsa_circ_295262,RMVar_hsa_circ_312643,RMVar_hsa_circ_164760,RMVar_hsa_circ_164761,RMVar_hsa_circ_327531,RMVar_hsa_circ_109154,RMVar_hsa_circ_164765,RMVar_hsa_circ_164763,RMVar_hsa_circ_325567,RMVar_hsa_circ_326199,RMVar_hsa_circ_164764,RMVar_hsa_circ_301088,RMVar_hsa_circ_295564,RMVar_hsa_circ_347313 8433 RMVar_ID_8433 Human_SNP_ID_545465136 A-to-I Human chr13 - 110693650 110693650 110693650 TTGACTTTTAGAATATGAGTTTCCAGCCGGACACGGTGGCTCACGCCTGTAATCCCAGCATTTTG TTGACTTTTAGAATATGAGTTTCCAGCCGGACGCGGTGGCTCACGCCTGTAATCCCAGCATTTTG T C CARS2 Ensembl:ENSG00000134905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs977818058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12097789 RMVar_hsa_circ_114303,RMVar_hsa_circ_164753,RMVar_hsa_circ_36728,RMVar_hsa_circ_40801,RMVar_hsa_circ_63373,RMVar_hsa_circ_367471,RMVar_hsa_circ_61249,RMVar_hsa_circ_295262,RMVar_hsa_circ_312643,RMVar_hsa_circ_164760,RMVar_hsa_circ_164761,RMVar_hsa_circ_327531,RMVar_hsa_circ_164765,RMVar_hsa_circ_326199,RMVar_hsa_circ_301088,RMVar_hsa_circ_295564,RMVar_hsa_circ_347313,RMVar_hsa_circ_70910,RMVar_hsa_circ_335882,RMVar_hsa_circ_371419,RMVar_hsa_circ_164766 8434 RMVar_ID_8434 Human_SNP_ID_545465243 A-to-I Human chr13 - 110694100 110694100 110694100 TCACTTAAACCTGGGAGGCAGAGGTTGCGGTGAGCTGAGATCGCACCATTGCACTCCAGCCTGGG TCACTTAAACCTGGGAGGCAGAGGTTGCGGTGGGCTGAGATCGCACCATTGCACTCCAGCCTGGG T C CARS2 Ensembl:ENSG00000134905 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1007171178 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114303,RMVar_hsa_circ_164753,RMVar_hsa_circ_36728,RMVar_hsa_circ_40801,RMVar_hsa_circ_63373,RMVar_hsa_circ_367471,RMVar_hsa_circ_61249,RMVar_hsa_circ_295262,RMVar_hsa_circ_312643,RMVar_hsa_circ_164760,RMVar_hsa_circ_164761,RMVar_hsa_circ_327531,RMVar_hsa_circ_164765,RMVar_hsa_circ_326199,RMVar_hsa_circ_301088,RMVar_hsa_circ_295564,RMVar_hsa_circ_347313,RMVar_hsa_circ_70910,RMVar_hsa_circ_335882,RMVar_hsa_circ_371419,RMVar_hsa_circ_164766 8435 RMVar_ID_8435 Human_SNP_ID_545465359 A-to-I Human chr13 - 110694585 110694585 110694585 TCATCCAGGCTGGAGTGCAATGGTGGGATCTCAGCCCAGCGCAACCTCCGCCTCCCAGGCTCAAG TCATCCAGGCTGGAGTGCAATGGTGGGATCTCGGCCCAGCGCAACCTCCGCCTCCCAGGCTCAAG T C CARS2 Ensembl:ENSG00000134905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1396612529 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114303,RMVar_hsa_circ_164753,RMVar_hsa_circ_36728,RMVar_hsa_circ_40801,RMVar_hsa_circ_63373,RMVar_hsa_circ_367471,RMVar_hsa_circ_61249,RMVar_hsa_circ_295262,RMVar_hsa_circ_312643,RMVar_hsa_circ_164760,RMVar_hsa_circ_164761,RMVar_hsa_circ_327531,RMVar_hsa_circ_164765,RMVar_hsa_circ_326199,RMVar_hsa_circ_301088,RMVar_hsa_circ_295564,RMVar_hsa_circ_347313,RMVar_hsa_circ_70910,RMVar_hsa_circ_335882,RMVar_hsa_circ_371419,RMVar_hsa_circ_164766 8436 RMVar_ID_8436 Human_SNP_ID_545466348 A-to-I Human chr13 - 110698889 110698889 110698889 TCCCACCTCAGCCCTCCTGGTAGCTGGGACTCAGCTGTGCACCACCACACATGACTAATTTTTTT TCCCACCTCAGCCCTCCTGGTAGCTGGGACTCCGCTGTGCACCACCACACATGACTAATTTTTTT T G CARS2 Ensembl:ENSG00000134905 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs916130270 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12097828 RMVar_hsa_circ_114303,RMVar_hsa_circ_164753,RMVar_hsa_circ_36728,RMVar_hsa_circ_40801,RMVar_hsa_circ_63373,RMVar_hsa_circ_367471,RMVar_hsa_circ_295262,RMVar_hsa_circ_312643,RMVar_hsa_circ_164760,RMVar_hsa_circ_164761,RMVar_hsa_circ_327531,RMVar_hsa_circ_164765,RMVar_hsa_circ_326199,RMVar_hsa_circ_301088,RMVar_hsa_circ_295564,RMVar_hsa_circ_347313,RMVar_hsa_circ_70910,RMVar_hsa_circ_335882,RMVar_hsa_circ_371419,RMVar_hsa_circ_164766 8437 RMVar_ID_8437 Human_SNP_ID_545469178 A-to-I Human chr13 - 110709211 110709207 110709211 ACATGCCTGTAATCCCAGCTACTCAGGAGACAAGCAGGAGAATTGCTTGAACCCGGGAGACGTGA ACATGCCTGTAATCCCAGCTACTCAGGAGACA____GGAGAATTGCTTGAACCCGGGAGACGTGA CTGCT C CARS2 Ensembl:ENSG00000134905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167908966 Functional Loss DEL dbSNP153 33..36 33 - - - 8438 RMVar_ID_8438 Human_SNP_ID_545473434 A-to-I Human chr13 + 110721325 110721325 110721325 AGATTGAGTTCCAGGCTGGAGTGCAATAGCGCAATCTTGGCTCACCGCAACCTCCGCCTCCCAGG AGATTGAGTTCCAGGCTGGAGTGCAATAGCGCCATCTTGGCTCACCGCAACCTCCGCCTCCCAGG A C ING1 Ensembl:ENSG00000153487 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs986300314 Functional Loss SNV dbSNP153 33..33 33 - - - 8439 RMVar_ID_8439 Human_SNP_ID_545516038 A-to-I Human chr13 - 110892249 110892249 110892249 ATTTGTATTTTTAGTAGAGAAGGGGCTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGGCCT ATTTGTATTTTTAGTAGAGAAGGGGCTTCACCGTGTTGGCCAGGCTGGTCTTGAACTCCTGGCCT T C ANKRD10 Ensembl:ENSG00000088448 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1394988993 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95018,RMVar_hsa_circ_126654,RMVar_hsa_circ_164770,RMVar_hsa_circ_164769,RMVar_hsa_circ_124905,RMVar_hsa_circ_164771 8440 RMVar_ID_8440 Human_SNP_ID_545517117 A-to-I Human chr13 - 110895411 110895411 110895411 CTCCGCTAATTTTTTGTATTTTTAGTAGAGCCAGGGTTTCATCATGTAAGCCAAGCTGGTCTCAA CTCCGCTAATTTTTTGTATTTTTAGTAGAGCCGGGGTTTCATCATGTAAGCCAAGCTGGTCTCAA T C ANKRD10,ANKRD10-IT1 Ensembl:ENSG00000088448,Ensembl:ENSG00000229152 Protein coding,lincRNA intron,intron GSE107867;GSE123020:GSM3490832,GSM3490833,GSM3490834 ASD brains,cerebellum;esophageal squamous carcinoma cells,KYSE180 cell line - 30559470,32596459 RNA-Seq:(High) rs1471118146 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2373435 RMVar_hsa_circ_95018,RMVar_hsa_circ_164770,RMVar_hsa_circ_124905,RMVar_hsa_circ_164771,RMVar_hsa_circ_355791,RMVar_hsa_circ_164774 8441 RMVar_ID_8441 Human_SNP_ID_545517140 A-to-I Human chr13 - 110895487 110895487 110895487 TGCCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCAGGGACTATAGGCATGTG TGCCTCCCAGGTTCAAGCGATTCTCCTGCCTCCGCCTCCCAAGTAGCAGGGACTATAGGCATGTG T G ANKRD10,ANKRD10-IT1 Ensembl:ENSG00000088448,Ensembl:ENSG00000229152 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1363338341 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95018,RMVar_hsa_circ_164770,RMVar_hsa_circ_124905,RMVar_hsa_circ_164771,RMVar_hsa_circ_355791,RMVar_hsa_circ_164774 8442 RMVar_ID_8442 Human_SNP_ID_545517145 A-to-I Human chr13 - 110895504 110895504 110895504 CGGCTCACTGCAGCCTCTGCCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCA CGGCTCACTGCAGCCTCTGCCTCCCAGGTTCAGGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCA T C ANKRD10,ANKRD10-IT1 Ensembl:ENSG00000088448,Ensembl:ENSG00000229152 Protein coding,lincRNA intron,intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 31158229,32596459 RNA-Seq:(High) rs1002535858 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95018,RMVar_hsa_circ_164770,RMVar_hsa_circ_124905,RMVar_hsa_circ_164771,RMVar_hsa_circ_355791,RMVar_hsa_circ_164774 8443 RMVar_ID_8443 Human_SNP_ID_545517147 A-to-I Human chr13 - 110895525 110895525 110895525 TGGAGTGCAGTGGTGTGATCTCGGCTCACTGCAGCCTCTGCCTCCCAGGTTCAAGCGATTCTCCT TGGAGTGCAGTGGTGTGATCTCGGCTCACTGCGGCCTCTGCCTCCCAGGTTCAAGCGATTCTCCT T C ANKRD10,ANKRD10-IT1 Ensembl:ENSG00000088448,Ensembl:ENSG00000229152 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1384507813 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95018,RMVar_hsa_circ_164770,RMVar_hsa_circ_124905,RMVar_hsa_circ_164771,RMVar_hsa_circ_355791,RMVar_hsa_circ_164774 8444 RMVar_ID_8444 Human_SNP_ID_545517164 A-to-I Human chr13 - 110895578 110895578 110895578 AATTGGTATTTATTTATTTATTTAGAGATAGAATCTTGCTCTGTTGCCCAGGCTGGAGTGCAGTG AATTGGTATTTATTTATTTATTTAGAGATAGAGTCTTGCTCTGTTGCCCAGGCTGGAGTGCAGTG T C ANKRD10,ANKRD10-IT1 Ensembl:ENSG00000088448,Ensembl:ENSG00000229152 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs985637618 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12098498 RMVar_hsa_circ_95018,RMVar_hsa_circ_164770,RMVar_hsa_circ_124905,RMVar_hsa_circ_164771,RMVar_hsa_circ_355791,RMVar_hsa_circ_164774 8445 RMVar_ID_8445 Human_SNP_ID_545517604 A-to-I Human chr13 - 110897219 110897219 110897219 GGAGGCTGAGGCTAAGGAGGATCCCTTAGCCCAGGAGTTCCAGGGTGTGGTGAACTATGATTGTG GGAGGCTGAGGCTAAGGAGGATCCCTTAGCCCGGGAGTTCCAGGGTGTGGTGAACTATGATTGTG T C ANKRD10,ANKRD10-IT1 Ensembl:ENSG00000088448,Ensembl:ENSG00000229152 Protein coding,lincRNA intron,intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1030763307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6257707,Human_RBP_ID_9028276,Human_RBP_ID_23585024,Human_RBP_ID_25076368 RMVar_hsa_circ_95018,RMVar_hsa_circ_164770,RMVar_hsa_circ_124905,RMVar_hsa_circ_164771,RMVar_hsa_circ_355791,RMVar_hsa_circ_164774 8446 RMVar_ID_8446 Human_SNP_ID_545517643 A-to-I Human chr13 - 110897296 110897296 110897296 AACATCTCTCAAAATTAAAAAAAAAAAAAAAAAAGTAGCCAGGCATGGTAGCACATGCCTGTATA AACATCTCTCAAAATTAAAAAAAAAAAAAAAAGAGTAGCCAGGCATGGTAGCACATGCCTGTATA T C ANKRD10,ANKRD10-IT1 Ensembl:ENSG00000088448,Ensembl:ENSG00000229152 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1362575876 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25032283 RMVar_hsa_circ_95018,RMVar_hsa_circ_164770,RMVar_hsa_circ_124905,RMVar_hsa_circ_164771,RMVar_hsa_circ_355791,RMVar_hsa_circ_164774 8447 RMVar_ID_8447 Human_SNP_ID_545517997 A-to-I Human chr13 - 110898648 110898648 110898648 GGAGCACCTGAGCCCAGGAGGTAGACGAGGCTACAGTGAGCTGTGATTGCACCACTGCACTCCAG GGAGCACCTGAGCCCAGGAGGTAGACGAGGCTGCAGTGAGCTGTGATTGCACCACTGCACTCCAG T C ANKRD10,ANKRD10-IT1 Ensembl:ENSG00000088448,Ensembl:ENSG00000229152 Protein coding,lincRNA intron,intron GSE100210;GSE99789;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,29796672,31158229,32596459 RNA-Seq:(High) rs996336952 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5087582,Human_RBP_ID_5246752,Human_RBP_ID_6257732,Human_RBP_ID_12098707,Human_RBP_ID_23159553 RMVar_hsa_circ_95018,RMVar_hsa_circ_164770,RMVar_hsa_circ_124905,RMVar_hsa_circ_164771,RMVar_hsa_circ_355791,RMVar_hsa_circ_164774 8448 RMVar_ID_8448 Human_SNP_ID_545518001 A-to-I Human chr13 - 110898665 110898665 110898665 AGGAGGCTGAAGTGGGAGGAGCACCTGAGCCCAGGAGGTAGACGAGGCTACAGTGAGCTGTGATT AGGAGGCTGAAGTGGGAGGAGCACCTGAGCCCGGGAGGTAGACGAGGCTACAGTGAGCTGTGATT T C ANKRD10,ANKRD10-IT1 Ensembl:ENSG00000088448,Ensembl:ENSG00000229152 Protein coding,lincRNA intron,intron GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831 HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line - 29129909,32596459 RNA-Seq:(High) rs1373436172 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3440545,Human_RBP_ID_5087582,Human_RBP_ID_5246752,Human_RBP_ID_6257732,Human_RBP_ID_8180801,Human_RBP_ID_9719265,Human_RBP_ID_12098707,Human_RBP_ID_25076379 RMVar_hsa_circ_95018,RMVar_hsa_circ_164770,RMVar_hsa_circ_124905,RMVar_hsa_circ_164771,RMVar_hsa_circ_355791,RMVar_hsa_circ_164774 8449 RMVar_ID_8449 Human_SNP_ID_545518028 A-to-I Human chr13 - 110898762 110898745 110898763 AACAAGAGTGAAACTCCGTCTCAAAAAAAAAAAAAAAAAAAAAAGAAAAGAAAAACTAGTTGGGT AACAAGAGTGAAACTCCGTCTCAAAAAAAAA__________________GAAAAACTAGTTGGGT CTTTTCTTTTTTTTTTTTT C ANKRD10,ANKRD10-IT1 Ensembl:ENSG00000088448,Ensembl:ENSG00000229152 Protein coding,lincRNA intron,intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs768736682 Functional Loss DEL dbSNP153 32..49 33 - - - Human_RBP_ID_9752650,Human_RBP_ID_22913742,Human_RBP_ID_25076380 RMVar_hsa_circ_95018,RMVar_hsa_circ_164770,RMVar_hsa_circ_124905,RMVar_hsa_circ_164771,RMVar_hsa_circ_355791,RMVar_hsa_circ_164774 8450 RMVar_ID_8450 Human_SNP_ID_545518034 A-to-I Human chr13 - 110898762 110898750 110898762 AACAAGAGTGAAACTCCGTCTCAAAAAAAAAAAAAAAAAAAAAAGAAAAGAAAAACTAGTTGGGT AACAAGAGTGAAACTCCGTCTCAAAAAAAAAA____________GAAAAGAAAAACTAGTTGGGT CTTTTTTTTTTTT C ANKRD10,ANKRD10-IT1 Ensembl:ENSG00000088448,Ensembl:ENSG00000229152 Protein coding,lincRNA intron,intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs56176208 Functional Loss DEL dbSNP153 33..44 33 - - - Human_RBP_ID_9752650,Human_RBP_ID_22913742,Human_RBP_ID_25076380 RMVar_hsa_circ_95018,RMVar_hsa_circ_164770,RMVar_hsa_circ_124905,RMVar_hsa_circ_164771,RMVar_hsa_circ_355791,RMVar_hsa_circ_164774 8451 RMVar_ID_8451 Human_SNP_ID_545518035 A-to-I Human chr13 - 110898762 110898750 110898762 AACAAGAGTGAAACTCCGTCTCAAAAAAAAAAAAAAAAAAAAAAGAAAAGAAAAACTAGTTGGGT AACAAGAGTGAAACTCCGTCTCAAAAAAAAAA___________AGAAAAGAAAAACTAGTTGGGT CTTTTTTTTTTTT CT ANKRD10,ANKRD10-IT1 Ensembl:ENSG00000088448,Ensembl:ENSG00000229152 Protein coding,lincRNA intron,intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs56176208 Functional Loss DEL dbSNP153 33..43 33 - - - Human_RBP_ID_9752650,Human_RBP_ID_22913742,Human_RBP_ID_25076380 RMVar_hsa_circ_95018,RMVar_hsa_circ_164770,RMVar_hsa_circ_124905,RMVar_hsa_circ_164771,RMVar_hsa_circ_355791,RMVar_hsa_circ_164774 8452 RMVar_ID_8452 Human_SNP_ID_545518036 A-to-I Human chr13 - 110898762 110898750 110898762 AACAAGAGTGAAACTCCGTCTCAAAAAAAAAAAAAAAAAAAAAAGAAAAGAAAAACTAGTTGGGT AACAAGAGTGAAACTCCGTCTCAAAAAAAAAA__________AAGAAAAGAAAAACTAGTTGGGT CTTTTTTTTTTTT CTT ANKRD10,ANKRD10-IT1 Ensembl:ENSG00000088448,Ensembl:ENSG00000229152 Protein coding,lincRNA intron,intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs56176208 Functional Loss DEL dbSNP153 33..42 33 - - - Human_RBP_ID_9752650,Human_RBP_ID_22913742,Human_RBP_ID_25076380 RMVar_hsa_circ_95018,RMVar_hsa_circ_164770,RMVar_hsa_circ_124905,RMVar_hsa_circ_164771,RMVar_hsa_circ_355791,RMVar_hsa_circ_164774 8453 RMVar_ID_8453 Human_SNP_ID_545518037 A-to-I Human chr13 - 110898762 110898750 110898762 AACAAGAGTGAAACTCCGTCTCAAAAAAAAAAAAAAAAAAAAAAGAAAAGAAAAACTAGTTGGGT AACAAGAGTGAAACTCCGTCTCAAAAAAAAAA_________AAAGAAAAGAAAAACTAGTTGGGT CTTTTTTTTTTTT CTTT ANKRD10,ANKRD10-IT1 Ensembl:ENSG00000088448,Ensembl:ENSG00000229152 Protein coding,lincRNA intron,intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs56176208 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_9752650,Human_RBP_ID_22913742,Human_RBP_ID_25076380 RMVar_hsa_circ_95018,RMVar_hsa_circ_164770,RMVar_hsa_circ_124905,RMVar_hsa_circ_164771,RMVar_hsa_circ_355791,RMVar_hsa_circ_164774 8454 RMVar_ID_8454 Human_SNP_ID_545518038 A-to-I Human chr13 - 110898762 110898750 110898762 AACAAGAGTGAAACTCCGTCTCAAAAAAAAAAAAAAAAAAAAAAGAAAAGAAAAACTAGTTGGGT AACAAGAGTGAAACTCCGTCTCAAAAAAAAAA________AAAAGAAAAGAAAAACTAGTTGGGT CTTTTTTTTTTTT CTTTT ANKRD10,ANKRD10-IT1 Ensembl:ENSG00000088448,Ensembl:ENSG00000229152 Protein coding,lincRNA intron,intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs56176208 Functional Loss DEL dbSNP153 33..40 33 - - - Human_RBP_ID_9752650,Human_RBP_ID_22913742,Human_RBP_ID_25076380 RMVar_hsa_circ_95018,RMVar_hsa_circ_164770,RMVar_hsa_circ_124905,RMVar_hsa_circ_164771,RMVar_hsa_circ_355791,RMVar_hsa_circ_164774 8455 RMVar_ID_8455 Human_SNP_ID_545518039 A-to-I Human chr13 - 110898762 110898750 110898762 AACAAGAGTGAAACTCCGTCTCAAAAAAAAAAAAAAAAAAAAAAGAAAAGAAAAACTAGTTGGGT AACAAGAGTGAAACTCCGTCTCAAAAAAAAAA_______AAAAAGAAAAGAAAAACTAGTTGGGT CTTTTTTTTTTTT CTTTTT ANKRD10,ANKRD10-IT1 Ensembl:ENSG00000088448,Ensembl:ENSG00000229152 Protein coding,lincRNA intron,intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs56176208 Functional Loss DEL dbSNP153 33..39 33 - - - Human_RBP_ID_9752650,Human_RBP_ID_22913742,Human_RBP_ID_25076380 RMVar_hsa_circ_95018,RMVar_hsa_circ_164770,RMVar_hsa_circ_124905,RMVar_hsa_circ_164771,RMVar_hsa_circ_355791,RMVar_hsa_circ_164774 8456 RMVar_ID_8456 Human_SNP_ID_545518040 A-to-I Human chr13 - 110898762 110898750 110898762 AACAAGAGTGAAACTCCGTCTCAAAAAAAAAAAAAAAAAAAAAAGAAAAGAAAAACTAGTTGGGT AACAAGAGTGAAACTCCGTCTCAAAAAAAAAA______AAAAAAGAAAAGAAAAACTAGTTGGGT CTTTTTTTTTTTT CTTTTTT ANKRD10,ANKRD10-IT1 Ensembl:ENSG00000088448,Ensembl:ENSG00000229152 Protein coding,lincRNA intron,intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs56176208 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_9752650,Human_RBP_ID_22913742,Human_RBP_ID_25076380 RMVar_hsa_circ_95018,RMVar_hsa_circ_164770,RMVar_hsa_circ_124905,RMVar_hsa_circ_164771,RMVar_hsa_circ_355791,RMVar_hsa_circ_164774 8457 RMVar_ID_8457 Human_SNP_ID_545518041 A-to-I Human chr13 - 110898762 110898750 110898762 AACAAGAGTGAAACTCCGTCTCAAAAAAAAAAAAAAAAAAAAAAGAAAAGAAAAACTAGTTGGGT AACAAGAGTGAAACTCCGTCTCAAAAAAAAAA_____AAAAAAAGAAAAGAAAAACTAGTTGGGT CTTTTTTTTTTTT CTTTTTTT ANKRD10,ANKRD10-IT1 Ensembl:ENSG00000088448,Ensembl:ENSG00000229152 Protein coding,lincRNA intron,intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs56176208 Functional Loss DEL dbSNP153 33..37 33 - - - Human_RBP_ID_9752650,Human_RBP_ID_22913742,Human_RBP_ID_25076380 RMVar_hsa_circ_95018,RMVar_hsa_circ_164770,RMVar_hsa_circ_124905,RMVar_hsa_circ_164771,RMVar_hsa_circ_355791,RMVar_hsa_circ_164774 8458 RMVar_ID_8458 Human_SNP_ID_545518042 A-to-I Human chr13 - 110898762 110898750 110898762 AACAAGAGTGAAACTCCGTCTCAAAAAAAAAAAAAAAAAAAAAAGAAAAGAAAAACTAGTTGGGT AACAAGAGTGAAACTCCGTCTCAAAAAAAAAA____AAAAAAAAGAAAAGAAAAACTAGTTGGGT CTTTTTTTTTTTT CTTTTTTTT ANKRD10,ANKRD10-IT1 Ensembl:ENSG00000088448,Ensembl:ENSG00000229152 Protein coding,lincRNA intron,intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs56176208 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_9752650,Human_RBP_ID_22913742,Human_RBP_ID_25076380 RMVar_hsa_circ_95018,RMVar_hsa_circ_164770,RMVar_hsa_circ_124905,RMVar_hsa_circ_164771,RMVar_hsa_circ_355791,RMVar_hsa_circ_164774 8459 RMVar_ID_8459 Human_SNP_ID_545518043 A-to-I Human chr13 - 110898762 110898750 110898762 AACAAGAGTGAAACTCCGTCTCAAAAAAAAAAAAAAAAAAAAAAGAAAAGAAAAACTAGTTGGGT AACAAGAGTGAAACTCCGTCTCAAAAAAAAAA___AAAAAAAAAGAAAAGAAAAACTAGTTGGGT CTTTTTTTTTTTT CTTTTTTTTT ANKRD10,ANKRD10-IT1 Ensembl:ENSG00000088448,Ensembl:ENSG00000229152 Protein coding,lincRNA intron,intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs56176208 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_9752650,Human_RBP_ID_22913742,Human_RBP_ID_25076380 RMVar_hsa_circ_95018,RMVar_hsa_circ_164770,RMVar_hsa_circ_124905,RMVar_hsa_circ_164771,RMVar_hsa_circ_355791,RMVar_hsa_circ_164774 8460 RMVar_ID_8460 Human_SNP_ID_545518044 A-to-I Human chr13 - 110898762 110898750 110898762 AACAAGAGTGAAACTCCGTCTCAAAAAAAAAAAAAAAAAAAAAAGAAAAGAAAAACTAGTTGGGT AACAAGAGTGAAACTCCGTCTCAAAAAAAAAA__AAAAAAAAAAGAAAAGAAAAACTAGTTGGGT CTTTTTTTTTTTT CTTTTTTTTTT ANKRD10,ANKRD10-IT1 Ensembl:ENSG00000088448,Ensembl:ENSG00000229152 Protein coding,lincRNA intron,intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs56176208 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_9752650,Human_RBP_ID_22913742,Human_RBP_ID_25076380 RMVar_hsa_circ_95018,RMVar_hsa_circ_164770,RMVar_hsa_circ_124905,RMVar_hsa_circ_164771,RMVar_hsa_circ_355791,RMVar_hsa_circ_164774 8461 RMVar_ID_8461 Human_SNP_ID_545518045 A-to-I Human chr13 - 110898762 110898750 110898762 AACAAGAGTGAAACTCCGTCTCAAAAAAAAAAAAAAAAAAAAAAGAAAAGAAAAACTAGTTGGGT AACAAGAGTGAAACTCCGTCTCAAAAAAAAAA_AAAAAAAAAAAGAAAAGAAAAACTAGTTGGGT CTTTTTTTTTTTT CTTTTTTTTTTT ANKRD10,ANKRD10-IT1 Ensembl:ENSG00000088448,Ensembl:ENSG00000229152 Protein coding,lincRNA intron,intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs56176208 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_9752650,Human_RBP_ID_22913742,Human_RBP_ID_25076380 RMVar_hsa_circ_95018,RMVar_hsa_circ_164770,RMVar_hsa_circ_124905,RMVar_hsa_circ_164771,RMVar_hsa_circ_355791,RMVar_hsa_circ_164774 8462 RMVar_ID_8462 Human_SNP_ID_545518058 A-to-I Human chr13 - 110898757 110898757 110898757 GAGTGAAACTCCGTCTCAAAAAAAAAAAAAAAAAAAAAAGAAAAGAAAAACTAGTTGGGTATGGT GAGTGAAACTCCGTCTCAAAAAAAAAAAAAAAGAAAAAAGAAAAGAAAAACTAGTTGGGTATGGT T C ANKRD10,ANKRD10-IT1 Ensembl:ENSG00000088448,Ensembl:ENSG00000229152 Protein coding,lincRNA intron,intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1218075367 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9752650,Human_RBP_ID_22913742,Human_RBP_ID_25076380 RMVar_hsa_circ_95018,RMVar_hsa_circ_164770,RMVar_hsa_circ_124905,RMVar_hsa_circ_164771,RMVar_hsa_circ_355791,RMVar_hsa_circ_164774 8463 RMVar_ID_8463 Human_SNP_ID_545518065 A-to-I Human chr13 - 110898762 110898762 110898762 AACAAGAGTGAAACTCCGTCTCAAAAAAAAAAAAAAAAAAAAAAGAAAAGAAAAACTAGTTGGGT AACAAGAGTGAAACTCCGTCTCAAAAAAAAAAGAAAAAAAAAAAGAAAAGAAAAACTAGTTGGGT T C ANKRD10,ANKRD10-IT1 Ensembl:ENSG00000088448,Ensembl:ENSG00000229152 Protein coding,lincRNA intron,intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs866506219 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9752650,Human_RBP_ID_22913742,Human_RBP_ID_25076380 RMVar_hsa_circ_95018,RMVar_hsa_circ_164770,RMVar_hsa_circ_124905,RMVar_hsa_circ_164771,RMVar_hsa_circ_355791,RMVar_hsa_circ_164774 8464 RMVar_ID_8464 Human_SNP_ID_545518127 A-to-I Human chr13 - 110898930 110898930 110898930 CAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTAGCTGGGTGTGGTGGTGGGCGCT CAACATGGTGAAACCCCGTCTCTACTAAAAATTCAAAAAATTAGCTGGGTGTGGTGGTGGGCGCT T A ANKRD10,ANKRD10-IT1 Ensembl:ENSG00000088448,Ensembl:ENSG00000229152 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1346798957 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95018,RMVar_hsa_circ_164770,RMVar_hsa_circ_124905,RMVar_hsa_circ_164771,RMVar_hsa_circ_355791,RMVar_hsa_circ_164774 8465 RMVar_ID_8465 Human_SNP_ID_545518150 A-to-I Human chr13 - 110899021 110899021 110899021 TGGACGCAGTGGCTCTCGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGTGGGTCATCTGA TGGACGCAGTGGCTCTCGCCTGTAATCCCAGCTCTTTGGGAGGCTGAGGTGGGTGGGTCATCTGA T A ANKRD10,ANKRD10-IT1 Ensembl:ENSG00000088448,Ensembl:ENSG00000229152 Protein coding,lincRNA intron,intron GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs556962981 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12098713,Human_RBP_ID_25032330 RMVar_hsa_circ_95018,RMVar_hsa_circ_164770,RMVar_hsa_circ_124905,RMVar_hsa_circ_164771,RMVar_hsa_circ_355791,RMVar_hsa_circ_164774 8466 RMVar_ID_8466 Human_SNP_ID_545518390 A-to-I Human chr13 - 110899961 110899961 110899961 GTGATCCTCCTGCTTCTGCCTCCCAAAGCGCCAGGATTATAGGGTTGAGCCACTGTGCTTGGCTT GTGATCCTCCTGCTTCTGCCTCCCAAAGCGCCGGGATTATAGGGTTGAGCCACTGTGCTTGGCTT T C ANKRD10 Ensembl:ENSG00000088448 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1137123 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6257756,Human_RBP_ID_9719293,Human_RBP_ID_25032357 RMVar_hsa_circ_95018,RMVar_hsa_circ_164770,RMVar_hsa_circ_124905,RMVar_hsa_circ_164771,RMVar_hsa_circ_355791,RMVar_hsa_circ_164774 8467 RMVar_ID_8467 Human_SNP_ID_545518391 A-to-I Human chr13 - 110899961 110899961 110899961 GTGATCCTCCTGCTTCTGCCTCCCAAAGCGCCAGGATTATAGGGTTGAGCCACTGTGCTTGGCTT GTGATCCTCCTGCTTCTGCCTCCCAAAGCGCCCGGATTATAGGGTTGAGCCACTGTGCTTGGCTT T G ANKRD10 Ensembl:ENSG00000088448 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1137123 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6257756,Human_RBP_ID_9719293,Human_RBP_ID_25032357 RMVar_hsa_circ_95018,RMVar_hsa_circ_164770,RMVar_hsa_circ_124905,RMVar_hsa_circ_164771,RMVar_hsa_circ_355791,RMVar_hsa_circ_164774 8468 RMVar_ID_8468 Human_SNP_ID_545518400 A-to-I Human chr13 - 110899994 110899994 110899994 TTGCCTAGGCTGGTCTCAAACTTCTGGCCTCAAGTGATCCTCCTGCTTCTGCCTCCCAAAGCGCC TTGCCTAGGCTGGTCTCAAACTTCTGGCCTCAGGTGATCCTCCTGCTTCTGCCTCCCAAAGCGCC T C ANKRD10 Ensembl:ENSG00000088448 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-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 8469 RMVar_ID_8469 Human_SNP_ID_545518412 A-to-I Human chr13 - 110900040 110900040 110900040 TCTTAGATATAAATTTGAGTGTTTGAAGAGACAGGGTCTTCCTGTGTTGCCTAGGCTGGTCTCAA TCTTAGATATAAATTTGAGTGTTTGAAGAGACGGGGTCTTCCTGTGTTGCCTAGGCTGGTCTCAA T C ANKRD10 Ensembl:ENSG00000088448 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1137121 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12098776 RMVar_hsa_circ_95018,RMVar_hsa_circ_164770,RMVar_hsa_circ_124905,RMVar_hsa_circ_164771,RMVar_hsa_circ_355791,RMVar_hsa_circ_164774 8470 RMVar_ID_8470 Human_SNP_ID_545518413 A-to-I Human chr13 - 110900040 110900040 110900040 TCTTAGATATAAATTTGAGTGTTTGAAGAGACAGGGTCTTCCTGTGTTGCCTAGGCTGGTCTCAA TCTTAGATATAAATTTGAGTGTTTGAAGAGACCGGGTCTTCCTGTGTTGCCTAGGCTGGTCTCAA T G ANKRD10 Ensembl:ENSG00000088448 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1137121 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12098776 RMVar_hsa_circ_95018,RMVar_hsa_circ_164770,RMVar_hsa_circ_124905,RMVar_hsa_circ_164771,RMVar_hsa_circ_355791,RMVar_hsa_circ_164774 8471 RMVar_ID_8471 Human_SNP_ID_546020808 A-to-I Human chr13 + 112793222 112793222 112793222 GCAGAGCCAGGGGCCCTTTCTTTTCATTTTTGAGACAGAGTCTCTCTCTGTGCCCAGGCTGGAGT GCAGAGCCAGGGGCCCTTTCTTTTCATTTTTGGGACAGAGTCTCTCTCTGTGCCCAGGCTGGAGT A G ATP11A Ensembl:ENSG00000068650 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs990445828 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22313,RMVar_hsa_circ_58855,RMVar_hsa_circ_113720,RMVar_hsa_circ_363297,RMVar_hsa_circ_368997,RMVar_hsa_circ_117988,RMVar_hsa_circ_97642,RMVar_hsa_circ_54690,RMVar_hsa_circ_164852,RMVar_hsa_circ_164854,RMVar_hsa_circ_164855,RMVar_hsa_circ_164856,RMVar_hsa_circ_164853 8472 RMVar_ID_8472 Human_SNP_ID_546095533 A-to-I Human chr13 - 113047797 113047797 113047797 GTAGCGAGGTGTGAGCAGAGGGGACGGGGCACACGTAGCGAGGCGTGAGCAGAGGGGACGGGGCA GTAGCGAGGTGTGAGCAGAGGGGACGGGGCACGCGTAGCGAGGCGTGAGCAGAGGGGACGGGGCA T C - - Other Unknown GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs932630840 Functional Loss SNV dbSNP153 33..33 33 - - - 8473 RMVar_ID_8473 Human_SNP_ID_546147134 A-to-I Human chr13 + 113222870 113222870 113222870 TGCAGTGAGCTGAGATTGCGCCACTGCACTCCAGCCTGAGCAGCAGAGCAAGACCCCCATCTCTA TGCAGTGAGCTGAGATTGCGCCACTGCACTCCTGCCTGAGCAGCAGAGCAAGACCCCCATCTCTA A T CUL4A Ensembl:ENSG00000139842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1207157294 Functional Loss SNV dbSNP153 33..33 33 - - - 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 8474 RMVar_ID_8474 Human_SNP_ID_546147297 A-to-I Human chr13 + 113223451 113223451 113223451 AGTTTCGCTCTTAATTGCCCAGGCTAGTGTGCAATGGCGCAATCTTGGCTCACCGCAACAACCTC AGTTTCGCTCTTAATTGCCCAGGCTAGTGTGCGATGGCGCAATCTTGGCTCACCGCAACAACCTC A G CUL4A Ensembl:ENSG00000139842 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1188851437 Functional Loss SNV dbSNP153 33..33 33 - - - 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 8475 RMVar_ID_8475 Human_SNP_ID_546147314 A-to-I Human chr13 + 113223515 113223515 113223515 CCACTCCTGGGTTCAAGCGATTCTCTTGTCTCAGCCTCCCGAGTAGCTGGGATTACAGGAATGCG CCACTCCTGGGTTCAAGCGATTCTCTTGTCTCTGCCTCCCGAGTAGCTGGGATTACAGGAATGCG A T CUL4A Ensembl:ENSG00000139842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1306769037 Functional Loss SNV dbSNP153 33..33 33 - - - 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 8476 RMVar_ID_8476 Human_SNP_ID_546155548 A-to-I Human chr13 + 113251519 113251519 113251519 TGTGTTCCTGCCCAAATCTCATATTGAATTGTAATCACCACTGCTGGGGGAGGGCCCGGGTGGGA TGTGTTCCTGCCCAAATCTCATATTGAATTGTGATCACCACTGCTGGGGGAGGGCCCGGGTGGGA A G CUL4A Ensembl:ENSG00000139842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1236689460 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 8477 RMVar_ID_8477 Human_SNP_ID_546160837 A-to-I Human chr13 + 113270946 113270946 113270946 ACAATTAGCCAGGCATGCTGGTGCTTGCCTGTAGTCCCAGCTTCTCAGGAGGCTGAGGTGGCAGG ACAATTAGCCAGGCATGCTGGTGCTTGCCTGTGGTCCCAGCTTCTCAGGAGGCTGAGGTGGCAGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1158077995 Functional Loss SNV dbSNP153 33..33 33 - - - 8478 RMVar_ID_8478 Human_SNP_ID_546168567 A-to-I Human chr13 + 113298984 113298984 113298984 CCAATATGGCGAAACCCGGTCTCTACAAAAATACAAAAATTAGCTGGGCATGGTGGCGCACGCCT CCAATATGGCGAAACCCGGTCTCTACAAAAATCCAAAAATTAGCTGGGCATGGTGGCGCACGCCT A C LAMP1 Ensembl:ENSG00000185896 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs923546293 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25034201 RMVar_hsa_circ_87658,RMVar_hsa_circ_164910 8479 RMVar_ID_8479 Human_SNP_ID_546168694 A-to-I Human chr13 + 113299430 113299430 113299430 GGGATTACAGGCACCCGCCACTATGCTAGGCTAATTTATGTATTTTTGGTAGAGACTAGGTTTAA GGGATTACAGGCACCCGCCACTATGCTAGGCTCATTTATGTATTTTTGGTAGAGACTAGGTTTAA A C LAMP1 Ensembl:ENSG00000185896 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs985776974 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87658,RMVar_hsa_circ_164910 8480 RMVar_ID_8480 Human_SNP_ID_546168785 A-to-I Human chr13 + 113299668 113299667 113299668 TCCGTTCACTGCAGCCTCCGCCTCTTGTGTTCAAGCAGTTCTCCTGCCTCAGCCTCCCTAGTAGC TCCGTTCACTGCAGCCTCCGCCTCTTGTGTTC_AGCAGTTCTCCTGCCTCAGCCTCCCTAGTAGC CA C LAMP1 Ensembl:ENSG00000185896 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1439975503 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_87658,RMVar_hsa_circ_164910 8481 RMVar_ID_8481 Human_SNP_ID_546169118 A-to-I Human chr13 + 113300697 113300697 113300697 AAAGTTAGCCAGGCGTAGTGGCACAGGCCTGTAGTCCCAGTTACTCAGGAGGCTGAGGCAGGAGA AAAGTTAGCCAGGCGTAGTGGCACAGGCCTGTGGTCCCAGTTACTCAGGAGGCTGAGGCAGGAGA A G LAMP1 Ensembl:ENSG00000185896 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1463223659 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12104427 RMVar_hsa_circ_87658,RMVar_hsa_circ_164910 8482 RMVar_ID_8482 Human_SNP_ID_546169318 A-to-I Human chr13 + 113301450 113301450 113301450 CGAGACCAGCCTGGGCAATATGGTGAAATCCCATCTCTACTAAAATACAAAAAAAATTAGTCGGG CGAGACCAGCCTGGGCAATATGGTGAAATCCCGTCTCTACTAAAATACAAAAAAAATTAGTCGGG A G LAMP1 Ensembl:ENSG00000185896 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs984056651 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87658,RMVar_hsa_circ_164910 8483 RMVar_ID_8483 Human_SNP_ID_546169336 A-to-I Human chr13 + 113301502 113301502 113301502 AAAATTAGTCGGGCATGGTGGCGTACCCCTGTAGTCATAGCTACTTGGAAGGCTGAGGTAGGAGA AAAATTAGTCGGGCATGGTGGCGTACCCCTGTGGTCATAGCTACTTGGAAGGCTGAGGTAGGAGA A G LAMP1 Ensembl:ENSG00000185896 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs759706933 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8388252 RMVar_hsa_circ_87658,RMVar_hsa_circ_164910 8484 RMVar_ID_8484 Human_SNP_ID_546177609 A-to-I Human chr13 + 113326468 113326468 113326468 GAGGCGGGTGGATCACCTAAAGTCAGGAGTTCAAGACCAGCCTGGCTGACATGGCTGAAACCCCG GAGGCGGGTGGATCACCTAAAGTCAGGAGTTCGAGACCAGCCTGGCTGACATGGCTGAAACCCCG A G GRTP1-AS1 RNACentral:URS00009BB3D2 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1018456512 Functional Loss SNV dbSNP153 33..33 33 - - - 8485 RMVar_ID_8485 Human_SNP_ID_546177627 A-to-I Human chr13 + 113326509 113326509 113326509 CTGGCTGACATGGCTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCCAGGTGTGGTGGTGG CTGGCTGACATGGCTGAAACCCCGTCTCTACTGAAAATACAAAAATTAGCCAGGTGTGGTGGTGG A G GRTP1-AS1 RNACentral:URS00009BB3D2 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1430587131 Functional Loss SNV dbSNP153 33..33 33 - - - 8486 RMVar_ID_8486 Human_SNP_ID_546186075 A-to-I Human chr13 - 113349312 113349312 113349312 TGGTGGCACACGCCTGTGGTCCCGGCTGCTCGAGGGGCTGAGGTGAGAGGGTCGTTTGGGTCTGG TGGTGGCACACGCCTGTGGTCCCGGCTGCTCGCGGGGCTGAGGTGAGAGGGTCGTTTGGGTCTGG T G GRTP1 Ensembl:ENSG00000139835 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs945246181 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_164931,RMVar_hsa_circ_284822,RMVar_hsa_circ_313492,RMVar_hsa_circ_164932 8487 RMVar_ID_8487 Human_SNP_ID_546187619 A-to-I Human chr13 - 113353819 113353819 113353819 AGGATTCGCCCTCCTTCACCTCCCAAAGTGCTAGGGTTACAGGAGTGAGCCACCCACCTGGCTGA AGGATTCGCCCTCCTTCACCTCCCAAAGTGCTGGGGTTACAGGAGTGAGCCACCCACCTGGCTGA T C GRTP1 Ensembl:ENSG00000139835 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs928850874 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_164931,RMVar_hsa_circ_284822,RMVar_hsa_circ_313492,RMVar_hsa_circ_164932,RMVar_hsa_circ_70767 8488 RMVar_ID_8488 Human_SNP_ID_546223103 A-to-I Human chr13 - 113466992 113466991 113466992 CACCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAAAATATAAAAAATTAGCCGGGCGTGG CACCCTGGCCAACATGGTGAAACCCCATCTCT_CTAAAAAAATATAAAAAATTAGCCGGGCGTGG GT G DCUN1D2 Ensembl:ENSG00000150401 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934861591 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_118957 RMVar_hsa_circ_305861,RMVar_hsa_circ_265899,RMVar_hsa_circ_66111 8489 RMVar_ID_8489 Human_SNP_ID_546237590 A-to-I Human chr13 + 113517372 113517372 113517372 CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCCGCCACCACGCCCGGCTAATTCTA CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTGCAGGCGCCCGCCACCACGCCCGGCTAATTCTA A G TMCO3 Ensembl:ENSG00000150403 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1434988244 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 8490 RMVar_ID_8490 Human_SNP_ID_546237591 A-to-I Human chr13 + 113517372 113517372 113517372 CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCCGCCACCACGCCCGGCTAATTCTA CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTTCAGGCGCCCGCCACCACGCCCGGCTAATTCTA A T TMCO3 Ensembl:ENSG00000150403 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1434988244 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 8491 RMVar_ID_8491 Human_SNP_ID_546237652 A-to-I Human chr13 + 113517435 113517433 113517435 TATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGGTCTCGATCTCCTGACCTCGTGA TATTTTTAGTAGAGACGGGGTTTCACCGTGT__GCCAGGATGGTCTCGATCTCCTGACCTCGTGA TTA T TMCO3 Ensembl:ENSG00000150403 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1566566885 Functional Loss DEL dbSNP153 32..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 8492 RMVar_ID_8492 Human_SNP_ID_546237653 A-to-I Human chr13 + 113517435 113517435 113517435 TATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGGTCTCGATCTCCTGACCTCGTGA TATTTTTAGTAGAGACGGGGTTTCACCGTGTTGGCCAGGATGGTCTCGATCTCCTGACCTCGTGA A G TMCO3 Ensembl:ENSG00000150403 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1045343135 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 8493 RMVar_ID_8493 Human_SNP_ID_546441601 A-to-I Human chr13 + 114237007 114237007 114237007 CCTGTAATCCCAGCGCTTTGGAAAGCCAAGGCAGGTGGATCATGAGGTCAGGAGCTCAAGACCAA CCTGTAATCCCAGCGCTTTGGAAAGCCAAGGCGGGTGGATCATGAGGTCAGGAGCTCAAGACCAA A G CDC16 Ensembl:ENSG00000130177 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1257725701 Functional Loss SNV dbSNP153 33..33 33 - - - 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_310485,RMVar_hsa_circ_287334,RMVar_hsa_circ_165017,RMVar_hsa_circ_10361,RMVar_hsa_circ_22296,RMVar_hsa_circ_165018,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 8494 RMVar_ID_8494 Human_SNP_ID_546443784 A-to-I Human chr13 + 114244495 114244492 114244496 TTTAATTGGCAAATACACATAACCTATTTATTAGTTTGGTGCAAAAGTAATTGCAGTTTTTGCTG TTTAATTGGCAAATACACATAACCTATTTA____TTTGGTGCAAAAGTAATTGCAGTTTTTGCTG ATTAG A CDC16 Ensembl:ENSG00000130177 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1389790216 Functional Loss DEL dbSNP153 31..34 33 - - - RMVar_hsa_circ_8428,RMVar_hsa_circ_25038,RMVar_hsa_circ_315999,RMVar_hsa_circ_323738,RMVar_hsa_circ_310485,RMVar_hsa_circ_287334,RMVar_hsa_circ_165017,RMVar_hsa_circ_10361,RMVar_hsa_circ_22296,RMVar_hsa_circ_165015,RMVar_hsa_circ_165016,RMVar_hsa_circ_300053,RMVar_hsa_circ_369628,RMVar_hsa_circ_374960,RMVar_hsa_circ_14592,RMVar_hsa_circ_25943,RMVar_hsa_circ_165020,RMVar_hsa_circ_165021,RMVar_hsa_circ_165022,RMVar_hsa_circ_4374,RMVar_hsa_circ_51356,RMVar_hsa_circ_110573,RMVar_hsa_circ_165024,RMVar_hsa_circ_376027,RMVar_hsa_circ_31480,RMVar_hsa_circ_31662,RMVar_hsa_circ_23041,RMVar_hsa_circ_165026,RMVar_hsa_circ_274870,RMVar_hsa_circ_293463,RMVar_hsa_circ_308520,RMVar_hsa_circ_165028,RMVar_hsa_circ_26725,RMVar_hsa_circ_165029,RMVar_hsa_circ_165027 8495 RMVar_ID_8495 Human_SNP_ID_546444611 A-to-I Human chr13 + 114247302 114247302 114247302 CCTCTTGCTCAGCCTCCCGAGTAGCTGGGACTACAGGCACCACCATGCCTAGCTGATTTAAACAT CCTCTTGCTCAGCCTCCCGAGTAGCTGGGACTTCAGGCACCACCATGCCTAGCTGATTTAAACAT A T CDC16 Ensembl:ENSG00000130177 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1457838676 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25035366 RMVar_hsa_circ_8428,RMVar_hsa_circ_25038,RMVar_hsa_circ_323738,RMVar_hsa_circ_310485,RMVar_hsa_circ_287334,RMVar_hsa_circ_165017,RMVar_hsa_circ_10361,RMVar_hsa_circ_165015,RMVar_hsa_circ_165016,RMVar_hsa_circ_300053,RMVar_hsa_circ_369628,RMVar_hsa_circ_14592,RMVar_hsa_circ_25943,RMVar_hsa_circ_165021,RMVar_hsa_circ_165022,RMVar_hsa_circ_51356,RMVar_hsa_circ_110573,RMVar_hsa_circ_165024,RMVar_hsa_circ_376027,RMVar_hsa_circ_165026,RMVar_hsa_circ_274870,RMVar_hsa_circ_308520,RMVar_hsa_circ_165028,RMVar_hsa_circ_26725,RMVar_hsa_circ_165027,RMVar_hsa_circ_105240,RMVar_hsa_circ_108925,RMVar_hsa_circ_37643,RMVar_hsa_circ_165030,RMVar_hsa_circ_165031,RMVar_hsa_circ_14604 8496 RMVar_ID_8496 Human_SNP_ID_546444647 A-to-I Human chr13 + 114247402 114247402 114247402 GTTGCCTAGGCTGGTCTTGAACTCCTGGCCTCAAGCAGTCCTCTTGCTTCGGCCTCCGAAAGTGT GTTGCCTAGGCTGGTCTTGAACTCCTGGCCTCGAGCAGTCCTCTTGCTTCGGCCTCCGAAAGTGT A G CDC16 Ensembl:ENSG00000130177 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs914241023 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17562099 RMVar_hsa_circ_8428,RMVar_hsa_circ_25038,RMVar_hsa_circ_323738,RMVar_hsa_circ_310485,RMVar_hsa_circ_287334,RMVar_hsa_circ_165017,RMVar_hsa_circ_10361,RMVar_hsa_circ_165015,RMVar_hsa_circ_165016,RMVar_hsa_circ_300053,RMVar_hsa_circ_369628,RMVar_hsa_circ_14592,RMVar_hsa_circ_25943,RMVar_hsa_circ_165021,RMVar_hsa_circ_165022,RMVar_hsa_circ_51356,RMVar_hsa_circ_110573,RMVar_hsa_circ_165024,RMVar_hsa_circ_376027,RMVar_hsa_circ_165026,RMVar_hsa_circ_274870,RMVar_hsa_circ_308520,RMVar_hsa_circ_165028,RMVar_hsa_circ_26725,RMVar_hsa_circ_165027,RMVar_hsa_circ_105240,RMVar_hsa_circ_108925,RMVar_hsa_circ_37643,RMVar_hsa_circ_165030,RMVar_hsa_circ_165031,RMVar_hsa_circ_14604 8497 RMVar_ID_8497 Human_SNP_ID_546444749 A-to-I Human chr13 + 114247743 114247743 114247743 ACTAAAAATACAAAAAATTAGCCAGATATAGTAGTGGGCATCTGCATCCCAGCTACTCGGGAGGC ACTAAAAATACAAAAAATTAGCCAGATATAGTCGTGGGCATCTGCATCCCAGCTACTCGGGAGGC A C CDC16 Ensembl:ENSG00000130177 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs979758875 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12107159 RMVar_hsa_circ_8428,RMVar_hsa_circ_25038,RMVar_hsa_circ_323738,RMVar_hsa_circ_310485,RMVar_hsa_circ_287334,RMVar_hsa_circ_165017,RMVar_hsa_circ_10361,RMVar_hsa_circ_165015,RMVar_hsa_circ_165016,RMVar_hsa_circ_300053,RMVar_hsa_circ_369628,RMVar_hsa_circ_14592,RMVar_hsa_circ_25943,RMVar_hsa_circ_165021,RMVar_hsa_circ_165022,RMVar_hsa_circ_51356,RMVar_hsa_circ_110573,RMVar_hsa_circ_165024,RMVar_hsa_circ_376027,RMVar_hsa_circ_165026,RMVar_hsa_circ_274870,RMVar_hsa_circ_308520,RMVar_hsa_circ_165028,RMVar_hsa_circ_26725,RMVar_hsa_circ_165027,RMVar_hsa_circ_105240,RMVar_hsa_circ_108925,RMVar_hsa_circ_37643,RMVar_hsa_circ_165030,RMVar_hsa_circ_165031,RMVar_hsa_circ_14604 8498 RMVar_ID_8498 Human_SNP_ID_546447694 A-to-I Human chr13 + 114258888 114258888 114258888 GGGAGGCCGAGATGGGCATATTGCTTGAGGCCAGGAGTTTGAGACCAGCATGTGCAACATGGCGA GGGAGGCCGAGATGGGCATATTGCTTGAGGCCCGGAGTTTGAGACCAGCATGTGCAACATGGCGA A C CDC16 Ensembl:ENSG00000130177 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs988868774 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8428,RMVar_hsa_circ_310485,RMVar_hsa_circ_287334,RMVar_hsa_circ_10361,RMVar_hsa_circ_165015,RMVar_hsa_circ_165016,RMVar_hsa_circ_369628,RMVar_hsa_circ_165022,RMVar_hsa_circ_51356,RMVar_hsa_circ_110573,RMVar_hsa_circ_165024,RMVar_hsa_circ_376027,RMVar_hsa_circ_165026,RMVar_hsa_circ_26725,RMVar_hsa_circ_58542,RMVar_hsa_circ_18979,RMVar_hsa_circ_105240,RMVar_hsa_circ_108925,RMVar_hsa_circ_37643,RMVar_hsa_circ_165030,RMVar_hsa_circ_165031,RMVar_hsa_circ_14604,RMVar_hsa_circ_332162,RMVar_hsa_circ_346182,RMVar_hsa_circ_165033,RMVar_hsa_circ_165034,RMVar_hsa_circ_344794,RMVar_hsa_circ_346617,RMVar_hsa_circ_77770,RMVar_hsa_circ_165035 8499 RMVar_ID_8499 Human_SNP_ID_546447707 A-to-I Human chr13 + 114258927 114258927 114258927 TGAGACCAGCATGTGCAACATGGCGAAACCCCATCTCTACTAAAAATACAGAAATTAGCCAGGGA TGAGACCAGCATGTGCAACATGGCGAAACCCCGTCTCTACTAAAAATACAGAAATTAGCCAGGGA A G CDC16 Ensembl:ENSG00000130177 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1412543422 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8428,RMVar_hsa_circ_310485,RMVar_hsa_circ_287334,RMVar_hsa_circ_10361,RMVar_hsa_circ_165015,RMVar_hsa_circ_165016,RMVar_hsa_circ_369628,RMVar_hsa_circ_165022,RMVar_hsa_circ_51356,RMVar_hsa_circ_110573,RMVar_hsa_circ_165024,RMVar_hsa_circ_376027,RMVar_hsa_circ_165026,RMVar_hsa_circ_26725,RMVar_hsa_circ_58542,RMVar_hsa_circ_18979,RMVar_hsa_circ_105240,RMVar_hsa_circ_108925,RMVar_hsa_circ_37643,RMVar_hsa_circ_165030,RMVar_hsa_circ_165031,RMVar_hsa_circ_14604,RMVar_hsa_circ_332162,RMVar_hsa_circ_346182,RMVar_hsa_circ_165033,RMVar_hsa_circ_165034,RMVar_hsa_circ_344794,RMVar_hsa_circ_346617,RMVar_hsa_circ_77770,RMVar_hsa_circ_165035 8500 RMVar_ID_8500 Human_SNP_ID_546448608 A-to-I Human chr13 - 114262675 114262675 114262675 TGCATCTTCCAGGCCCACTCCCTCCGCCGGCCAAGGGCACTCCTGCAGGGATGTCTGCTGTATTC TGCATCTTCCAGGCCCACTCCCTCCGCCGGCCGAGGGCACTCCTGCAGGGATGTCTGCTGTATTC T C lnc-RASA3-7 RNACentral:URS0000D5D69D lincRNA intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs549046174 Functional Loss SNV dbSNP153 33..33 33 - - - 8501 RMVar_ID_8501 Human_SNP_ID_546449052 A-to-I Human chr13 + 114264431 114264431 114264431 AGCTGGGCATGGTAGCACATGCCTGTAGTCCCAGCTACTAGCCCTGCGCCCGGTCCCAGGCTGAG AGCTGGGCATGGTAGCACATGCCTGTAGTCCCGGCTACTAGCCCTGCGCCCGGTCCCAGGCTGAG A G CDC16 Ensembl:ENSG00000130177 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs17338298 Functional Loss SNV dbSNP153,EGP 33..33 33 - - - RMVar_hsa_circ_8428,RMVar_hsa_circ_310485,RMVar_hsa_circ_165015,RMVar_hsa_circ_110573,RMVar_hsa_circ_165024,RMVar_hsa_circ_376027,RMVar_hsa_circ_165026,RMVar_hsa_circ_26725,RMVar_hsa_circ_58542,RMVar_hsa_circ_18979,RMVar_hsa_circ_105240,RMVar_hsa_circ_108925,RMVar_hsa_circ_165030,RMVar_hsa_circ_165031,RMVar_hsa_circ_332162,RMVar_hsa_circ_165033,RMVar_hsa_circ_165034,RMVar_hsa_circ_344794,RMVar_hsa_circ_77770,RMVar_hsa_circ_316600,RMVar_hsa_circ_165035,RMVar_hsa_circ_338933 8502 RMVar_ID_8502 Human_SNP_ID_546449131 A-to-I Human chr13 + 114264673 114264673 114264673 TTGCTTTGTCGCCTAGGCTAGAGTGCAGTGGTACGATCTCGGCTCACTGCAACCTCCACCTCCCA TTGCTTTGTCGCCTAGGCTAGAGTGCAGTGGTGCGATCTCGGCTCACTGCAACCTCCACCTCCCA A G CDC16 Ensembl:ENSG00000130177 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1009551442 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8428,RMVar_hsa_circ_310485,RMVar_hsa_circ_165015,RMVar_hsa_circ_110573,RMVar_hsa_circ_165024,RMVar_hsa_circ_376027,RMVar_hsa_circ_165026,RMVar_hsa_circ_26725,RMVar_hsa_circ_58542,RMVar_hsa_circ_18979,RMVar_hsa_circ_105240,RMVar_hsa_circ_108925,RMVar_hsa_circ_165030,RMVar_hsa_circ_165031,RMVar_hsa_circ_332162,RMVar_hsa_circ_165033,RMVar_hsa_circ_165034,RMVar_hsa_circ_344794,RMVar_hsa_circ_77770,RMVar_hsa_circ_316600,RMVar_hsa_circ_165035,RMVar_hsa_circ_338933 8503 RMVar_ID_8503 Human_SNP_ID_546449173 A-to-I Human chr13 + 114264869 114264869 114264869 AGCCCAGGTGATCCACCCGTCTAGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGCGC AGCCCAGGTGATCCACCCGTCTAGGCCTCCCAGAGTGCTGGGATTACAGGCATGAGCCACTGCGC A G CDC16 Ensembl:ENSG00000130177 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569608310 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8428,RMVar_hsa_circ_310485,RMVar_hsa_circ_165015,RMVar_hsa_circ_110573,RMVar_hsa_circ_165024,RMVar_hsa_circ_376027,RMVar_hsa_circ_165026,RMVar_hsa_circ_26725,RMVar_hsa_circ_58542,RMVar_hsa_circ_18979,RMVar_hsa_circ_105240,RMVar_hsa_circ_108925,RMVar_hsa_circ_165030,RMVar_hsa_circ_165031,RMVar_hsa_circ_332162,RMVar_hsa_circ_165033,RMVar_hsa_circ_165034,RMVar_hsa_circ_344794,RMVar_hsa_circ_77770,RMVar_hsa_circ_316600,RMVar_hsa_circ_165035,RMVar_hsa_circ_338933 8504 RMVar_ID_8504 Human_SNP_ID_546454623 A-to-I Human chr13 + 114283121 114283121 114283121 TCACGGCTCACTGCAGCCTCACACTGCGGCTCAAGCAATCCTCCAGCCTCCTAGGTAGCAGGGAC TCACGGCTCACTGCAGCCTCACACTGCGGCTCCAGCAATCCTCCAGCCTCCTAGGTAGCAGGGAC A C UPF3A Ensembl:ENSG00000169062 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1332304890 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9028700,Human_RBP_ID_12107457 Human_miRNA_ID_2715114,Human_miRNA_ID_3051097 RMVar_hsa_circ_119268,RMVar_hsa_circ_50978,RMVar_hsa_circ_165038 8505 RMVar_ID_8505 Human_SNP_ID_546454669 A-to-I Human chr13 + 114283267 114283267 114283267 GTCTTGAACTCCTGGCTTCAAGTGATCCTCCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGC GTCTTGAACTCCTGGCTTCAAGTGATCCTCCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGC A G UPF3A Ensembl:ENSG00000169062 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1211735556 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_118286 RMVar_hsa_circ_119268,RMVar_hsa_circ_50978,RMVar_hsa_circ_165038 8506 RMVar_ID_8506 Human_SNP_ID_546454908 A-to-I Human chr13 + 114284102 114284102 114284102 AAAATATTGGTGGGCCGGGCACAGTGGCTCACACCTGTAATCCCAGCACTTTAGGAGGCCAAGGC AAAATATTGGTGGGCCGGGCACAGTGGCTCACGCCTGTAATCCCAGCACTTTAGGAGGCCAAGGC A G UPF3A Ensembl:ENSG00000169062 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1278983366 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50978 8507 RMVar_ID_8507 Human_SNP_ID_546454979 A-to-I Human chr13 + 114284322 114284322 114284322 AGGCGGAGGTTGCAGTGAGCCGAGATCATGCCACTGCATCCCAGCCGGGGCGACGGAGCAAAAAA AGGCGGAGGTTGCAGTGAGCCGAGATCATGCCGCTGCATCCCAGCCGGGGCGACGGAGCAAAAAA A G UPF3A Ensembl:ENSG00000169062 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1250276883 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23159592,Human_RBP_ID_23587017,Human_RBP_ID_25076817 RMVar_hsa_circ_50978 8508 RMVar_ID_8508 Human_SNP_ID_546455031 A-to-I Human chr13 + 114284419 114284419 114284419 GTGTGTGTGTGTAAAATATGTGTAACATGGCCAGGTGTGATGGCTCACTCCTGTAATCCCAGCAC GTGTGTGTGTGTAAAATATGTGTAACATGGCCGGGTGTGATGGCTCACTCCTGTAATCCCAGCAC A G UPF3A Ensembl:ENSG00000169062 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1266065204 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9720718,Human_RBP_ID_23159593,Human_RBP_ID_23587021,Human_RBP_ID_25076819 RMVar_hsa_circ_50978 8509 RMVar_ID_8509 Human_SNP_ID_546455294 A-to-I Human chr13 + 114285389 114285389 114285389 ATCTGCCATTGAATGAGTATCCACTGTGTGCTAGGCCTTGTGGGTGGAGCGGTGACTTGGACATC ATCTGCCATTGAATGAGTATCCACTGTGTGCTGGGCCTTGTGGGTGGAGCGGTGACTTGGACATC A G UPF3A Ensembl:ENSG00000169062 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1481390699 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6260504,Human_RBP_ID_12107528,Human_RBP_ID_17114931,Human_RBP_ID_23587029 RMVar_hsa_circ_50978 8510 RMVar_ID_8510 Human_SNP_ID_546455869 A-to-I Human chr13 + 114287374 114287374 114287374 TGTACTTTGGGAGGCCAGGGTGGGCGGATCACAAGGTCAGGACTTCGAGATCAGCCTGGCCGACA TGTACTTTGGGAGGCCAGGGTGGGCGGATCACGAGGTCAGGACTTCGAGATCAGCCTGGCCGACA A G UPF3A Ensembl:ENSG00000169062 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs373503791 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20767,RMVar_hsa_circ_366978 8511 RMVar_ID_8511 Human_SNP_ID_546455870 A-to-I Human chr13 + 114287380 114287380 114287380 TTGGGAGGCCAGGGTGGGCGGATCACAAGGTCAGGACTTCGAGATCAGCCTGGCCGACATGGTGA TTGGGAGGCCAGGGTGGGCGGATCACAAGGTCGGGACTTCGAGATCAGCCTGGCCGACATGGTGA A G UPF3A Ensembl:ENSG00000169062 Protein coding intron GSE38233;GSE100210;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,cerebellum - 24183664,29129909,30559470 RNA-Seq:(High) rs1371073445 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20767,RMVar_hsa_circ_366978 8512 RMVar_ID_8512 Human_SNP_ID_546455915 A-to-I Human chr13 + 114287468 114287468 114287468 AAAAAATTAGCAGGGCATGGTGGTGCGTGCCTATAGTTCCAGCTACTGAGGAGGCTGAGGCAGGA AAAAAATTAGCAGGGCATGGTGGTGCGTGCCTGTAGTTCCAGCTACTGAGGAGGCTGAGGCAGGA A G UPF3A Ensembl:ENSG00000169062 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1478006647 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20767,RMVar_hsa_circ_366978 8513 RMVar_ID_8513 Human_SNP_ID_546455917 A-to-I Human chr13 + 114287470 114287470 114287470 AAAATTAGCAGGGCATGGTGGTGCGTGCCTATAGTTCCAGCTACTGAGGAGGCTGAGGCAGGAGA AAAATTAGCAGGGCATGGTGGTGCGTGCCTATGGTTCCAGCTACTGAGGAGGCTGAGGCAGGAGA A G UPF3A Ensembl:ENSG00000169062 Protein coding intron GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs978372893 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20767,RMVar_hsa_circ_366978 8514 RMVar_ID_8514 Human_SNP_ID_546455940 A-to-I Human chr13 + 114287548 114287548 114287548 AGAAGGCGGAGGTTGCAGTGAGCTGAGATCGCACCACTGCACTCCAGCCTGGTGACAGAGCGAGA AGAAGGCGGAGGTTGCAGTGAGCTGAGATCGCGCCACTGCACTCCAGCCTGGTGACAGAGCGAGA A G UPF3A Ensembl:ENSG00000169062 Protein coding intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs936854766 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20767,RMVar_hsa_circ_366978 8515 RMVar_ID_8515 Human_SNP_ID_546456093 A-to-I Human chr13 + 114287948 114287948 114287948 TCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCACCCGCCATCATGCCCAGCTAATTTTTAT TCTGCCTCAGCCTCCTGAGTAGCTGGGATTACGGGCACCCGCCATCATGCCCAGCTAATTTTTAT A G UPF3A Ensembl:ENSG00000169062 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1461943646 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20767,RMVar_hsa_circ_366978 8516 RMVar_ID_8516 Human_SNP_ID_546464482 A-to-I Human chr13 + 114316194 114316194 114316194 TTTGTTTTTGTTTTTTAATGAGCCAGAGTTTCACTTTTGTTGCCTGGGCTGGAGTGCAGTTATGC TTTGTTTTTGTTTTTTAATGAGCCAGAGTTTCCCTTTTGTTGCCTGGGCTGGAGTGCAGTTATGC A C CHAMP1 Ensembl:ENSG00000198824 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1485032765 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12107666 8517 RMVar_ID_8517 Human_SNP_ID_546464865 A-to-I Human chr13 + 114317364 114317364 114317364 TAATTTCTTAAAGGCCAGGCATGGTAGCTCACACCTGTAATCCCAGCACTTTGAGAGGCCAAGGC TAATTTCTTAAAGGCCAGGCATGGTAGCTCACGCCTGTAATCCCAGCACTTTGAGAGGCCAAGGC A G CHAMP1 Ensembl:ENSG00000198824 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256454809 Functional Loss SNV dbSNP153 33..33 33 - - - 8518 RMVar_ID_8518 Human_SNP_ID_546464913 A-to-I Human chr13 + 114317549 114317549 114317549 AGGAGGCTGAGGCGGGGGGATCTCTGGAGCCCAGGAGTATGAGGCTGCAGTGAGTTGTGATGGCG AGGAGGCTGAGGCGGGGGGATCTCTGGAGCCCGGGAGTATGAGGCTGCAGTGAGTTGTGATGGCG A G CHAMP1 Ensembl:ENSG00000198824 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs908489963 Functional Loss SNV dbSNP153 33..33 33 - - - 8519 RMVar_ID_8519 Human_SNP_ID_260506242 A-to-I Human chr5 + 167580882 167580882 167580882 GTGGTGGCGCAAGCTTGTAATACCAGGTACTCAGGAGGCTGAGGCACCAGAATTGCTTGAACCCA GTGGTGGCGCAAGCTTGTAATACCAGGTACTCGGGAGGCTGAGGCACCAGAATTGCTTGAACCCA A G TENM2 Ensembl:ENSG00000145934 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1461559890 Functional Loss SNV dbSNP153 33..33 33 - - - 8520 RMVar_ID_8520 Human_SNP_ID_260523420 A-to-I Human chr5 + 167651085 167651085 167651085 CATCCTCATTTTATAGGAAATCATGTCATCCTACTTGAAGTGTGGCTGAAGAAAAACAATTAGAT CATCCTCATTTTATAGGAAATCATGTCATCCTGCTTGAAGTGTGGCTGAAGAAAAACAATTAGAT A G TENM2 Ensembl:ENSG00000145934 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1158873795 Functional Loss SNV dbSNP153 33..33 33 - - - 8521 RMVar_ID_8521 Human_SNP_ID_260523434 A-to-I Human chr5 + 167651140 167651140 167651140 ACAATTAGATGAATACTCCTCAGCAGTCTCCAAATAAGAACTACCTTGCACACTAATTTCCATTG ACAATTAGATGAATACTCCTCAGCAGTCTCCAGATAAGAACTACCTTGCACACTAATTTCCATTG A G TENM2 Ensembl:ENSG00000145934 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs191022324 Functional Loss SNV dbSNP153 33..33 33 - - - 8522 RMVar_ID_8522 Human_SNP_ID_260759543 A-to-I Human chr5 - 168577566 168577566 168577566 GAGAGGCCGAGGCGGGAGAATCGCTGGAGGCCAGGAGTTCGAGACCAACCTGGGCACCATAGTGA GAGAGGCCGAGGCGGGAGAATCGCTGGAGGCCGGGAGTTCGAGACCAACCTGGGCACCATAGTGA T C PANK3 Ensembl:ENSG00000120137 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917765689 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9099,RMVar_hsa_circ_116149,RMVar_hsa_circ_236054 8523 RMVar_ID_8523 Human_SNP_ID_261013000 A-to-I Human chr5 + 169593433 169593433 169593433 GCAGCTGAAGCACCAAGTAGATCATCAGAAGGAACTCCTCTCTTGTAAATCAGAGGAACTGCGCG GCAGCTGAAGCACCAAGTAGATCATCAGAAGGGACTCCTCTCTTGTAAATCAGAGGAACTGCGCG A G SPDL1 Ensembl:ENSG00000040275 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1368845561 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1040511,Human_RBP_ID_8887970,Human_RBP_ID_9305452,Human_RBP_ID_15371993,Human_RBP_ID_22511954,Human_RBP_ID_24095488,Human_RBP_ID_26351722,Human_RBP_ID_27077609,Human_RBP_ID_27827082 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 8524 RMVar_ID_8524 Human_SNP_ID_261051646 A-to-I Human chr5 + 169749232 169749232 169749232 TATGAAAATCCCTGAGGCTAAATTTGGCCCTTAGAGCAAATTGAAAAAGAGATGAAGCCCCTTTC TATGAAAATCCCTGAGGCTAAATTTGGCCCTTGGAGCAAATTGAAAAAGAGATGAAGCCCCTTTC A G DOCK2 Ensembl:ENSG00000134516 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs549493564 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11448,RMVar_hsa_circ_236106,RMVar_hsa_circ_107698,RMVar_hsa_circ_373338,RMVar_hsa_circ_375534,RMVar_hsa_circ_236107,RMVar_hsa_circ_236108,RMVar_hsa_circ_236110,RMVar_hsa_circ_369379,RMVar_hsa_circ_371060,RMVar_hsa_circ_99424,RMVar_hsa_circ_236115,RMVar_hsa_circ_236116,RMVar_hsa_circ_65399,RMVar_hsa_circ_48811,RMVar_hsa_circ_91965,RMVar_hsa_circ_269429,RMVar_hsa_circ_236118,RMVar_hsa_circ_336954,RMVar_hsa_circ_236119 8525 RMVar_ID_8525 Human_SNP_ID_261458662 A-to-I Human chr5 + 171394227 171394227 171394227 CCATGCCCTGCTAATTTTTGTATTTAGTAGAGACAGGGTTTCAGTATGTTGGTCCGGCTGGTCTT CCATGCCCTGCTAATTTTTGTATTTAGTAGAGGCAGGGTTTCAGTATGTTGGTCCGGCTGGTCTT A G NPM1 Ensembl:ENSG00000181163 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956006547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15375264 RMVar_hsa_circ_236205,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_338950,RMVar_hsa_circ_369661,RMVar_hsa_circ_321568,RMVar_hsa_circ_71541,RMVar_hsa_circ_82192,RMVar_hsa_circ_236207,RMVar_hsa_circ_236206,RMVar_hsa_circ_124069,RMVar_hsa_circ_236204,RMVar_hsa_circ_236212,RMVar_hsa_circ_113410,RMVar_hsa_circ_371528,RMVar_hsa_circ_120080,RMVar_hsa_circ_236216,RMVar_hsa_circ_236217,RMVar_hsa_circ_236215,RMVar_hsa_circ_108249,RMVar_hsa_circ_236219 8526 RMVar_ID_8526 Human_SNP_ID_261458673 A-to-I Human chr5 + 171394268 171394268 171394268 CAGTATGTTGGTCCGGCTGGTCTTGAACTCCTAACCTCGTGATCTACCTGCCTCGGTCTCCCAAA CAGTATGTTGGTCCGGCTGGTCTTGAACTCCTGACCTCGTGATCTACCTGCCTCGGTCTCCCAAA A G NPM1 Ensembl:ENSG00000181163 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1410496183 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7415276,Human_RBP_ID_8609764,Human_RBP_ID_15375268 RMVar_hsa_circ_236205,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_338950,RMVar_hsa_circ_369661,RMVar_hsa_circ_321568,RMVar_hsa_circ_71541,RMVar_hsa_circ_82192,RMVar_hsa_circ_236207,RMVar_hsa_circ_236206,RMVar_hsa_circ_124069,RMVar_hsa_circ_236204,RMVar_hsa_circ_236212,RMVar_hsa_circ_113410,RMVar_hsa_circ_371528,RMVar_hsa_circ_120080,RMVar_hsa_circ_236216,RMVar_hsa_circ_236217,RMVar_hsa_circ_236215,RMVar_hsa_circ_108249,RMVar_hsa_circ_236219 8527 RMVar_ID_8527 Human_SNP_ID_261459464 A-to-I Human chr5 + 171396852 171396852 171396852 ACATACAGCTGGGTGTGATGGTGGGCGCTTGCAATCCCAGCTGCTGGGGAGGCTGAGGCAGGAGA ACATACAGCTGGGTGTGATGGTGGGCGCTTGCGATCCCAGCTGCTGGGGAGGCTGAGGCAGGAGA A G NPM1 Ensembl:ENSG00000181163 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1315565076 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_236205,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_338950,RMVar_hsa_circ_369661,RMVar_hsa_circ_321568,RMVar_hsa_circ_71541,RMVar_hsa_circ_82192,RMVar_hsa_circ_236207,RMVar_hsa_circ_236206,RMVar_hsa_circ_124069,RMVar_hsa_circ_236204,RMVar_hsa_circ_236212,RMVar_hsa_circ_113410,RMVar_hsa_circ_371528,RMVar_hsa_circ_120080,RMVar_hsa_circ_236216,RMVar_hsa_circ_236217,RMVar_hsa_circ_236215,RMVar_hsa_circ_108249,RMVar_hsa_circ_236219 8528 RMVar_ID_8528 Human_SNP_ID_261460176 A-to-I Human chr5 + 171399054 171399054 171399054 TGTATTTTTAGTAGAGACTGGGTTTCCCCATTAGCCAGGCTGGTCTCAAACTCCTGACCTCAGGT TGTATTTTTAGTAGAGACTGGGTTTCCCCATTGGCCAGGCTGGTCTCAAACTCCTGACCTCAGGT A G NPM1 Ensembl:ENSG00000181163 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1372497594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2916031 RMVar_hsa_circ_236205,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_338950,RMVar_hsa_circ_369661,RMVar_hsa_circ_321568,RMVar_hsa_circ_71541,RMVar_hsa_circ_82192,RMVar_hsa_circ_236207,RMVar_hsa_circ_236206,RMVar_hsa_circ_124069,RMVar_hsa_circ_236204,RMVar_hsa_circ_236212,RMVar_hsa_circ_113410,RMVar_hsa_circ_371528,RMVar_hsa_circ_120080,RMVar_hsa_circ_236216,RMVar_hsa_circ_236217,RMVar_hsa_circ_236215,RMVar_hsa_circ_108249,RMVar_hsa_circ_236219 8529 RMVar_ID_8529 Human_SNP_ID_261460312 A-to-I Human chr5 + 171399498 171399498 171399498 AACTAAAACGATCCTCCCACCTCAGCCTCCCAAAGTGTTAGGATTATAGGTGTGAGACACTGTGC AACTAAAACGATCCTCCCACCTCAGCCTCCCAGAGTGTTAGGATTATAGGTGTGAGACACTGTGC A G NPM1 Ensembl:ENSG00000181163 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1026785926 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10195378,Human_RBP_ID_15375616 RMVar_hsa_circ_236205,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_338950,RMVar_hsa_circ_369661,RMVar_hsa_circ_321568,RMVar_hsa_circ_71541,RMVar_hsa_circ_82192,RMVar_hsa_circ_236207,RMVar_hsa_circ_236206,RMVar_hsa_circ_124069,RMVar_hsa_circ_236204,RMVar_hsa_circ_236212,RMVar_hsa_circ_113410,RMVar_hsa_circ_371528,RMVar_hsa_circ_120080,RMVar_hsa_circ_236216,RMVar_hsa_circ_236217,RMVar_hsa_circ_236215,RMVar_hsa_circ_108249,RMVar_hsa_circ_236219 8530 RMVar_ID_8530 Human_SNP_ID_261460901 A-to-I Human chr5 + 171401215 171401215 171401215 CCCTGTCTTTACTAAAAACACAAAAATTAGCCAGGCATGGTGGTATGTGCCTGTAATTCCACCTA CCCTGTCTTTACTAAAAACACAAAAATTAGCCGGGCATGGTGGTATGTGCCTGTAATTCCACCTA A G NPM1 Ensembl:ENSG00000181163 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs943797723 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17575578 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_236220,RMVar_hsa_circ_371814,RMVar_hsa_circ_236223,RMVar_hsa_circ_113068,RMVar_hsa_circ_367789,RMVar_hsa_circ_236222 8531 RMVar_ID_8531 Human_SNP_ID_261461038 A-to-I Human chr5 + 171401611 171401611 171401611 TGCGCGTGCCACCAGGCCCAGCGTATTTTTGTATTTTTGAGTAGAGATGGGGTTTCACTCTATAT TGCGCGTGCCACCAGGCCCAGCGTATTTTTGTGTTTTTGAGTAGAGATGGGGTTTCACTCTATAT A G NPM1 Ensembl:ENSG00000181163 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1424506162 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10195398 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_236220,RMVar_hsa_circ_371814,RMVar_hsa_circ_236223,RMVar_hsa_circ_113068,RMVar_hsa_circ_367789,RMVar_hsa_circ_236222 8532 RMVar_ID_8532 Human_SNP_ID_261461050 A-to-I Human chr5 + 171401671 171401671 171401671 TATATGTTGGCCAGGCTGGTCTCAAACCCCTGACTGCAGGTGATCCGCCCTCCTGGGCCTCTCAA TATATGTTGGCCAGGCTGGTCTCAAACCCCTGTCTGCAGGTGATCCGCCCTCCTGGGCCTCTCAA A T NPM1 Ensembl:ENSG00000181163 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1022804821 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15375758,Human_RBP_ID_17575579,Human_RBP_ID_26792209 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_236220,RMVar_hsa_circ_371814,RMVar_hsa_circ_236223,RMVar_hsa_circ_113068,RMVar_hsa_circ_367789,RMVar_hsa_circ_236222 8533 RMVar_ID_8533 Human_SNP_ID_261463723 A-to-I Human chr5 + 171409445 171409444 171409446 ATGGTGGCATGTACCTGTAATCCCACCTACTCAAGAGGCGGAGGCAGGAGGATCGCTTGAACCTG ATGGTGGCATGTACCTGTAATCCCACCTACTC__GAGGCGGAGGCAGGAGGATCGCTTGAACCTG CAA C NPM1 Ensembl:ENSG00000181163 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1220988451 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_15376080,Human_RBP_ID_21945342 RMVar_hsa_circ_113410,RMVar_hsa_circ_236217 8534 RMVar_ID_8534 Human_SNP_ID_261586301 A-to-I Human chr5 - 171904181 171904181 171904181 AAGTGGTTCTCGCGCGCCTCATCCTGCCAAGTAGCTGGGATTACAGGCGTGTGCCACCATGGCTA AAGTGGTTCTCGCGCGCCTCATCCTGCCAAGTGGCTGGGATTACAGGCGTGTGCCACCATGGCTA T C FBXW11 Ensembl:ENSG00000072803 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1304372189 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_969,RMVar_hsa_circ_314149,RMVar_hsa_circ_307292,RMVar_hsa_circ_308816,RMVar_hsa_circ_236232,RMVar_hsa_circ_1216,RMVar_hsa_circ_236234,RMVar_hsa_circ_370630,RMVar_hsa_circ_272395,RMVar_hsa_circ_7914,RMVar_hsa_circ_53462,RMVar_hsa_circ_274061,RMVar_hsa_circ_312101,RMVar_hsa_circ_354833,RMVar_hsa_circ_236238 8535 RMVar_ID_8535 Human_SNP_ID_261596662 A-to-I Human chr5 - 171947109 171947109 171947109 TTTAGTGGTGAAAGAAAATGAGTAAAACGGCCAGGTGCAGTGGCTCACGCCTGTAATCCCAGCAC TTTAGTGGTGAAAGAAAATGAGTAAAACGGCCGGGTGCAGTGGCTCACGCCTGTAATCCCAGCAC T C FBXW11 Ensembl:ENSG00000072803 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1392612953 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_307292,RMVar_hsa_circ_272395,RMVar_hsa_circ_274061,RMVar_hsa_circ_24827,RMVar_hsa_circ_236240,RMVar_hsa_circ_35660,RMVar_hsa_circ_318073,RMVar_hsa_circ_236241 8536 RMVar_ID_8536 Human_SNP_ID_261602701 A-to-I Human chr5 - 171971790 171971789 171971790 TTTGTAGAGATAAGGTTTCACTGTGTTGCCCAAGCTGGTGTTGAACTCCTGTGCTCAAGCAGTCC TTTGTAGAGATAAGGTTTCACTGTGTTGCCCA_GCTGGTGTTGAACTCCTGTGCTCAAGCAGTCC CT C FBXW11 Ensembl:ENSG00000072803 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432596249 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_15379413 RMVar_hsa_circ_307292,RMVar_hsa_circ_272395,RMVar_hsa_circ_274061,RMVar_hsa_circ_24827,RMVar_hsa_circ_318073,RMVar_hsa_circ_236241,RMVar_hsa_circ_307831 8537 RMVar_ID_8537 Human_SNP_ID_261606547 A-to-I Human chr5 - 171987603 171987603 171987603 CTAAAAATACAAAAAAAGTAGCTGGGCATGGTAGTGGGTGCCTGTAATCCCAGCTGCTCGGGAGG CTAAAAATACAAAAAAAGTAGCTGGGCATGGTGGTGGGTGCCTGTAATCCCAGCTGCTCGGGAGG T C FBXW11 Ensembl:ENSG00000072803 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1180055379 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25879330 RMVar_hsa_circ_307292,RMVar_hsa_circ_272395,RMVar_hsa_circ_274061,RMVar_hsa_circ_24827,RMVar_hsa_circ_318073,RMVar_hsa_circ_236241,RMVar_hsa_circ_307831 8538 RMVar_ID_8538 Human_SNP_ID_261620881 A-to-I Human chr5 - 172045737 172045737 172045737 TGCAGTGAGCCAAGATAGTGCCACTGCACTCCAGCCTGGGCGACAGAGCAAAACTCTGTCTCAAA TGCAGTGAGCCAAGATAGTGCCACTGCACTCCCGCCTGGGCGACAGAGCAAAACTCTGTCTCAAA T G STK10 Ensembl:ENSG00000072786 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1368001702 Functional Loss SNV dbSNP153 33..33 33 - - - 8539 RMVar_ID_8539 Human_SNP_ID_261622568 A-to-I Human chr5 - 172051541 172051541 172051541 AGCTCACTGCAACCTCTGCCTCCTGGGTTCAAATGATTTTCCTGCCTCAACCTCCTGAATAGCTG AGCTCACTGCAACCTCTGCCTCCTGGGTTCAAGTGATTTTCCTGCCTCAACCTCCTGAATAGCTG T C STK10 Ensembl:ENSG00000072786 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1350225283 Functional Loss SNV dbSNP153 33..33 33 - - - 8540 RMVar_ID_8540 Human_SNP_ID_261635227 A-to-I Human chr5 - 172097313 172097313 172097313 CATTGAGGCTGGGCACAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGTGG CATTGAGGCTGGGCACAGTGGCTCACGCCTGTGATCCCAGCACTTTGGGAGGCTGAGGCGGGTGG T C STK10 Ensembl:ENSG00000072786 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1315282645 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 8541 RMVar_ID_8541 Human_SNP_ID_261638452 A-to-I Human chr5 - 172108508 172108508 172108508 GGGTTCAAGCGATTTTTGTGCCTCAGCCCCCCAAGTATCTGGGATTACAGGCGTCCACCACCACA GGGTTCAAGCGATTTTTGTGCCTCAGCCCCCCCAGTATCTGGGATTACAGGCGTCCACCACCACA T G STK10 Ensembl:ENSG00000072786 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1022288624 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_28961,RMVar_hsa_circ_268016,RMVar_hsa_circ_15818,RMVar_hsa_circ_378668 8542 RMVar_ID_8542 Human_SNP_ID_261638576 A-to-I Human chr5 - 172108931 172108931 172108931 AAAATACAAAAATTAGCTGGGCATGTCGGCACATGCCTGTAATGTCATCTACTTGGGAGGCTGAG AAAATACAAAAATTAGCTGGGCATGTCGGCACGTGCCTGTAATGTCATCTACTTGGGAGGCTGAG T C STK10 Ensembl:ENSG00000072786 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs760382672 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_28961,RMVar_hsa_circ_268016,RMVar_hsa_circ_15818,RMVar_hsa_circ_378668 8543 RMVar_ID_8543 Human_SNP_ID_261638607 A-to-I Human chr5 - 172109060 172109060 172109060 ATCAGTAAGGCCGGGCGCAGTGGCTCACGCCTATAATCCCAGCACTTTGGAAGGCCAAGGCTGGT ATCAGTAAGGCCGGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGAAGGCCAAGGCTGGT T C STK10 Ensembl:ENSG00000072786 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs865828701 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_28961,RMVar_hsa_circ_268016,RMVar_hsa_circ_15818,RMVar_hsa_circ_378668 8544 RMVar_ID_8544 Human_SNP_ID_261639566 A-to-I Human chr5 - 172112823 172112823 172112823 AGAATTGCTTGAACCCGGAAGGTGGAGGTTGCAGTGAGCCGAGATCGTGCCATTGCACTCCAGCC AGAATTGCTTGAACCCGGAAGGTGGAGGTTGCGGTGAGCCGAGATCGTGCCATTGCACTCCAGCC T C STK10 Ensembl:ENSG00000072786 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1049389399 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_28961,RMVar_hsa_circ_268016,RMVar_hsa_circ_15818,RMVar_hsa_circ_378668 8545 RMVar_ID_8545 Human_SNP_ID_261639811 A-to-I Human chr5 - 172113850 172113850 172113850 GGAGTGCAATGGCACGATCTTAGCTCTCCACAACCGCTGCCTCCTGGGTTCAAGCGATTCTCTTG GGAGTGCAATGGCACGATCTTAGCTCTCCACATCCGCTGCCTCCTGGGTTCAAGCGATTCTCTTG T A STK10 Ensembl:ENSG00000072786 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs748043442 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_28961,RMVar_hsa_circ_268016,RMVar_hsa_circ_15818,RMVar_hsa_circ_378668 8546 RMVar_ID_8546 Human_SNP_ID_261640592 A-to-I Human chr5 - 172116275 172116275 172116275 GAGTTCAGGACCAGCCTGGCCAACATGGCGAAACCCCAATCTCTACTAAAAATACAAAAATTAGC GAGTTCAGGACCAGCCTGGCCAACATGGCGAATCCCCAATCTCTACTAAAAATACAAAAATTAGC T A STK10 Ensembl:ENSG00000072786 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1396002390 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_28961,RMVar_hsa_circ_268016,RMVar_hsa_circ_15818,RMVar_hsa_circ_378668 8547 RMVar_ID_8547 Human_SNP_ID_261640813 A-to-I Human chr5 - 172117086 172117086 172117086 TTAGTAGAGATGAGGTTTCACCATGTTGGCCAAGCTGGTCTCGAACTCCTCATCTCAAGTGATCT TTAGTAGAGATGAGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTCATCTCAAGTGATCT T C STK10 Ensembl:ENSG00000072786 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1445522302 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_28961,RMVar_hsa_circ_268016,RMVar_hsa_circ_15818,RMVar_hsa_circ_378668 8548 RMVar_ID_8548 Human_SNP_ID_261640822 A-to-I Human chr5 - 172117131 172117131 172117131 GGGATCACAGGCACCTGCCACCATGCCTGGCTACTTTTTGTACTTTTAGTAGAGATGAGGTTTCA GGGATCACAGGCACCTGCCACCATGCCTGGCTGCTTTTTGTACTTTTAGTAGAGATGAGGTTTCA T C STK10 Ensembl:ENSG00000072786 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1471503982 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_28961,RMVar_hsa_circ_268016,RMVar_hsa_circ_15818,RMVar_hsa_circ_378668 8549 RMVar_ID_8549 Human_SNP_ID_261640836 A-to-I Human chr5 - 172117203 172117203 172117203 GCGTTCTTGGCTCACTGCAACCTCCACCTCCCAGGTTCAAGTGCTTCTTGTGTTTCAGCCTCCCA GCGTTCTTGGCTCACTGCAACCTCCACCTCCCGGGTTCAAGTGCTTCTTGTGTTTCAGCCTCCCA T C STK10 Ensembl:ENSG00000072786 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1007953445 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_28961,RMVar_hsa_circ_268016,RMVar_hsa_circ_15818,RMVar_hsa_circ_378668 8550 RMVar_ID_8550 Human_SNP_ID_261643223 A-to-I Human chr5 - 172126756 172126756 172126756 ACCCACACATTCAGTAAATGCTCTGTGGGGACAGTGTCAGGTCTCAATGTCCTGGGCAAGCTTGA ACCCACACATTCAGTAAATGCTCTGTGGGGACGGTGTCAGGTCTCAATGTCCTGGGCAAGCTTGA T C STK10 Ensembl:ENSG00000072786 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs12655697 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_651 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_28961,RMVar_hsa_circ_301851,RMVar_hsa_circ_268016,RMVar_hsa_circ_338816 8551 RMVar_ID_8551 Human_SNP_ID_261657595 A-to-I Human chr5 - 172182824 172182824 172182824 AAATTGGCCGGGCGCGGTGGCTCACACCTGTAATCTCAGCACTTTGAGAGGCTGAATTGGGTGGA AAATTGGCCGGGCGCGGTGGCTCACACCTGTAGTCTCAGCACTTTGAGAGGCTGAATTGGGTGGA T C STK10 Ensembl:ENSG00000072786 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs59194263 Functional Loss SNV dbSNP153 33..33 33 - - - 8552 RMVar_ID_8552 Human_SNP_ID_261658455 A-to-I Human chr5 - 172186257 172186257 172186257 TTTTTATTTTTTGTGAGACGGAGTCTCACTCTATTGCCCAAGCTGGAGTGCGGTGGTTTGATCTC TTTTTATTTTTTGTGAGACGGAGTCTCACTCTGTTGCCCAAGCTGGAGTGCGGTGGTTTGATCTC T C STK10 Ensembl:ENSG00000072786 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs60897994 Functional Loss SNV dbSNP153 33..33 33 - - - 8553 RMVar_ID_8553 Human_SNP_ID_261680150 A-to-I Human chr5 - 172269239 172269239 172269239 ATGATCCACCTGCCTTGGCCTCCCGAAGTGCTAGGATTACAGGCATGAGCCACCCCGCCCCGCCC ATGATCCACCTGCCTTGGCCTCCCGAAGTGCTGGGATTACAGGCATGAGCCACCCCGCCCCGCCC T C UBTD2 Ensembl:ENSG00000168246 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1330348304 Functional Loss SNV dbSNP153 33..33 33 - - - 8554 RMVar_ID_8554 Human_SNP_ID_261680161 A-to-I Human chr5 - 172269279 172269274 172269279 CACCGTGTCAGCCAGACTGGTCTCCAACTCCTAACCTTAAATGATCCACCTGCCTTGGCCTCCCG CACCGTGTCAGCCAGACTGGTCTCCAACTCCT_____TAAATGATCCACCTGCCTTGGCCTCCCG AAGGTT A UBTD2 Ensembl:ENSG00000168246 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1289940739 Functional Loss DEL dbSNP153 33..37 33 - - - Human_RBP_ID_15380783 8555 RMVar_ID_8555 Human_SNP_ID_261682677 A-to-I Human chr5 - 172278467 172278467 172278467 CTGCCTAGGCTGGAATGCAATGGTGTGATCTCAGCTCGCTGCAACCTCTACCTCCCAGGTTCAAG CTGCCTAGGCTGGAATGCAATGGTGTGATCTCTGCTCGCTGCAACCTCTACCTCCCAGGTTCAAG T A UBTD2 Ensembl:ENSG00000168246 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1223955699 Functional Loss SNV dbSNP153 33..33 33 - - - 8556 RMVar_ID_8556 Human_SNP_ID_261686511 A-to-I Human chr5 + 172292730 172292730 172292730 TCGGGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCATGTGCCACCAAGCCTG TCGGGCAATTCTCCTGCCTCAGCCTCCCGAGTGGCTGGGATTACAGGCATGTGCCACCAAGCCTG A G LOC100288254,RF00017-4552 RNACentral:URS00008121BF,RNACentral:URS0000973F83 lincRNA,SRP RNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1392591377 Functional Loss SNV dbSNP153 33..33 33 - - - 8557 RMVar_ID_8557 Human_SNP_ID_261707317 A-to-I Human chr5 - 172369526 172369526 172369526 TGACCTCATGATCCGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCGC TGACCTCATGATCCGCCCACCTCGGCCTCCCAGAGTGCTGGGATTACAGGCGTGAGCCACTGCGC T C SH3PXD2B Ensembl:ENSG00000174705 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs749306375 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2013,RMVar_hsa_circ_68703,RMVar_hsa_circ_236254,RMVar_hsa_circ_115205,RMVar_hsa_circ_355035,RMVar_hsa_circ_313365,RMVar_hsa_circ_24991,RMVar_hsa_circ_5625,RMVar_hsa_circ_236256 8558 RMVar_ID_8558 Human_SNP_ID_261708832 A-to-I Human chr5 - 172376106 172376106 172376106 AGAATCGTTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCCAAGATCACACCACTGCACTCCAGCC AGAATCGTTTGAACCTGGGAGGCAGAGGTTGCGGTGAGCCAAGATCACACCACTGCACTCCAGCC T C SH3PXD2B Ensembl:ENSG00000174705 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1262774003 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2013,RMVar_hsa_circ_68703,RMVar_hsa_circ_236254,RMVar_hsa_circ_115205,RMVar_hsa_circ_355035,RMVar_hsa_circ_24991,RMVar_hsa_circ_5625,RMVar_hsa_circ_236256 8559 RMVar_ID_8559 Human_SNP_ID_261708843 A-to-I Human chr5 - 172376170 172376170 172376170 ACAAAAAGAGCCAGGCGTGGTGGTGGGCGTCTATAATCCCAGCTACATGGGAGGCTGAGGCAGGA ACAAAAAGAGCCAGGCGTGGTGGTGGGCGTCTGTAATCCCAGCTACATGGGAGGCTGAGGCAGGA T C SH3PXD2B Ensembl:ENSG00000174705 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs573448207 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2013,RMVar_hsa_circ_68703,RMVar_hsa_circ_236254,RMVar_hsa_circ_115205,RMVar_hsa_circ_355035,RMVar_hsa_circ_24991,RMVar_hsa_circ_5625,RMVar_hsa_circ_236256 8560 RMVar_ID_8560 Human_SNP_ID_261709785 A-to-I Human chr5 - 172380150 172380150 172380150 AGGAAGCTGAGATGGGAGAATTGCTCGGGCCAAGGAGGTTGAGGCTGCAGTGAGCAGTGATCGCC AGGAAGCTGAGATGGGAGAATTGCTCGGGCCAGGGAGGTTGAGGCTGCAGTGAGCAGTGATCGCC T C SH3PXD2B Ensembl:ENSG00000174705 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1030488774 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2013,RMVar_hsa_circ_68703,RMVar_hsa_circ_236254,RMVar_hsa_circ_115205,RMVar_hsa_circ_355035,RMVar_hsa_circ_24991,RMVar_hsa_circ_5625,RMVar_hsa_circ_236256 8561 RMVar_ID_8561 Human_SNP_ID_261709789 A-to-I Human chr5 - 172380178 172380177 172380178 TGGTACGTGCCTGTAGTCCCAGATACTCAGGAAGCTGAGATGGGAGAATTGCTCGGGCCAAGGAG TGGTACGTGCCTGTAGTCCCAGATACTCAGGA_GCTGAGATGGGAGAATTGCTCGGGCCAAGGAG CT C SH3PXD2B Ensembl:ENSG00000174705 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1235613425 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_2013,RMVar_hsa_circ_68703,RMVar_hsa_circ_236254,RMVar_hsa_circ_115205,RMVar_hsa_circ_355035,RMVar_hsa_circ_24991,RMVar_hsa_circ_5625,RMVar_hsa_circ_236256 8562 RMVar_ID_8562 Human_SNP_ID_261716799 A-to-I Human chr5 - 172409194 172409194 172409194 TGTATTTTTAGTGGAGAGGGGGTTTCACTGTTAGTCAGGCTGGTCTCGATCTCCTGACCTCAGGC TGTATTTTTAGTGGAGAGGGGGTTTCACTGTTTGTCAGGCTGGTCTCGATCTCCTGACCTCAGGC T A SH3PXD2B Ensembl:ENSG00000174705 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1561927652 Functional Loss SNV dbSNP153 33..33 33 - - - 8563 RMVar_ID_8563 Human_SNP_ID_261778452 A-to-I Human chr5 + 172656559 172656559 172656559 TGCCAGATTTCTTAATTCCACCTATGGCCAAGAGCCCCTTCCCCGCGGCCTTCGCTTTTAGCTCC TGCCAGATTTCTTAATTCCACCTATGGCCAAGGGCCCCTTCCCCGCGGCCTTCGCTTTTAGCTCC A G NEURL1B Ensembl:ENSG00000214357 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs879113195 Functional Loss SNV dbSNP153 33..33 33 - - - 8564 RMVar_ID_8564 Human_SNP_ID_261805803 A-to-I Human chr5 + 172766751 172766751 172766751 GACACTGATTCTGCGTAAAGACCTTGAACAACAGGACAGGACCAGAACCATAGCACAGGGTGCTC GACACTGATTCTGCGTAAAGACCTTGAACAACGGGACAGGACCAGAACCATAGCACAGGGTGCTC A G AC022217.4 Ensembl:ENSG00000253736 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1359805111 Functional Loss SNV dbSNP153 33..33 33 - - - 8565 RMVar_ID_8565 Human_SNP_ID_261830603 A-to-I Human chr5 + 172864058 172864058 172864058 CTCTACTAGAAATACAAAAAAATTAGCTGGGCATGGTGGTGCATACTTGTAGTCCTAGCTACTCG CTCTACTAGAAATACAAAAAAATTAGCTGGGCGTGGTGGTGCATACTTGTAGTCCTAGCTACTCG A G ERGIC1 Ensembl:ENSG00000113719 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1273862698 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_236263,RMVar_hsa_circ_122533 8566 RMVar_ID_8566 Human_SNP_ID_261849865 A-to-I Human chr5 + 172938900 172938900 172938900 CCTGACCAACATTGTGAAACCCCATCTCCACTAAAAGTACAAAAAATTAGCCGGGCATGGTGGCA CCTGACCAACATTGTGAAACCCCATCTCCACTGAAAGTACAAAAAATTAGCCGGGCATGGTGGCA A G ERGIC1 Ensembl:ENSG00000113719 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1241705902 Functional Loss SNV dbSNP153 33..33 33 - - - 8567 RMVar_ID_8567 Human_SNP_ID_261850450 A-to-I Human chr5 + 172941210 172941210 172941210 AGTTGGAGGCTGAGACAGGAGATCTTGGCAGTAAGCCAAGATCGTGCCACTGCACTCCAGCTCTG AGTTGGAGGCTGAGACAGGAGATCTTGGCAGTCAGCCAAGATCGTGCCACTGCACTCCAGCTCTG A C ERGIC1 Ensembl:ENSG00000113719 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1274493156 Functional Loss SNV dbSNP153 33..33 33 - - - 8568 RMVar_ID_8568 Human_SNP_ID_261851998 A-to-I Human chr5 + 172947452 172947452 172947452 CTTCCATCTCCCGAAGTGCTGAGATGACAGGCATGAGCCACTGTGCCCAGCTGAGTTATCTCAGC CTTCCATCTCCCGAAGTGCTGAGATGACAGGCGTGAGCCACTGTGCCCAGCTGAGTTATCTCAGC A G ERGIC1 Ensembl:ENSG00000113719 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs960621670 Functional Loss SNV dbSNP153 33..33 33 - - - 8569 RMVar_ID_8569 Human_SNP_ID_261853860 A-to-I Human chr5 - 172954346 172954346 172954346 CCAGACTGGTCTCAAACTCTTGGGCTCAAGCAATCCTCTCACCTCAGCCTCCCGGTGCTGGGATT CCAGACTGGTCTCAAACTCTTGGGCTCAAGCAGTCCTCTCACCTCAGCCTCCCGGTGCTGGGATT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992880745 Functional Loss SNV dbSNP153 33..33 33 - - - 8570 RMVar_ID_8570 Human_SNP_ID_261854179 A-to-I Human chr5 - 172955214 172955214 172955214 TGAAACAGGAGAACTGCTTGAATCTGGGAGGTAGATGTTGCAGTGAGCCGATATCGCGCCATTGC TGAAACAGGAGAACTGCTTGAATCTGGGAGGTGGATGTTGCAGTGAGCCGATATCGCGCCATTGC T C AC008429.1 Ensembl:ENSG00000204758 lincRNA intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1207172773 Functional Loss SNV dbSNP153 33..33 33 - - - 8571 RMVar_ID_8571 Human_SNP_ID_261864797 A-to-I Human chr5 + 172993325 172993325 172993325 GAGGCCAGGAGTTTGAGAACAGCCTGGACAACATGGCAAAACCCCATCTCTACTAAAAATACAAA GAGGCCAGGAGTTTGAGAACAGCCTGGACAACGTGGCAAAACCCCATCTCTACTAAAAATACAAA A G ATP6V0E1 Ensembl:ENSG00000113732 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1485115704 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_236281,RMVar_hsa_circ_127736 8572 RMVar_ID_8572 Human_SNP_ID_261865357 A-to-I Human chr5 + 172995643 172995643 172995643 TAAGGATTTCTTTCAATTTAGGTTTTTGAGACAGGGTCTTGCTCTGTCACCCAGGCTGGAATGGC TAAGGATTTCTTTCAATTTAGGTTTTTGAGACGGGGTCTTGCTCTGTCACCCAGGCTGGAATGGC A G ATP6V0E1 Ensembl:ENSG00000113732 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs779400776 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122921,RMVar_hsa_circ_236281,RMVar_hsa_circ_127736,RMVar_hsa_circ_294558,RMVar_hsa_circ_236282 8573 RMVar_ID_8573 Human_SNP_ID_261865369 A-to-I Human chr5 + 172995714 172995714 172995714 ATAGCTCACTGCAGCCTCAAACTCTTAGGCTCAGGCGATCCTCCTGCCTCTGCCTCCCAAGTAGT ATAGCTCACTGCAGCCTCAAACTCTTAGGCTCGGGCGATCCTCCTGCCTCTGCCTCCCAAGTAGT A G ATP6V0E1 Ensembl:ENSG00000113732 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs955870871 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122921,RMVar_hsa_circ_236281,RMVar_hsa_circ_127736,RMVar_hsa_circ_294558,RMVar_hsa_circ_236282 8574 RMVar_ID_8574 Human_SNP_ID_261865920 A-to-I Human chr5 + 172998043 172998043 172998043 AGGTGTGAGGATCACCTGAGCCCGGGGAAGTCAAGGCTACAGTGAGCTGTCATTGCGGCAGTGCA AGGTGTGAGGATCACCTGAGCCCGGGGAAGTCGAGGCTACAGTGAGCTGTCATTGCGGCAGTGCA A G ATP6V0E1 Ensembl:ENSG00000113732 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs369993724 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122921,RMVar_hsa_circ_236281,RMVar_hsa_circ_127736,RMVar_hsa_circ_294558,RMVar_hsa_circ_236282 8575 RMVar_ID_8575 Human_SNP_ID_261866296 A-to-I Human chr5 + 172999423 172999421 172999424 ATAGTTCACTGCAGCCTCAAACTCCTGGGCTGAAGCAATCTTCCTGCCTCAGCCTCCTGAGTAGC ATAGTTCACTGCAGCCTCAAACTCCTGGGCT___GCAATCTTCCTGCCTCAGCCTCCTGAGTAGC TGAA T ATP6V0E1 Ensembl:ENSG00000113732 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1291487124 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_122921,RMVar_hsa_circ_236281,RMVar_hsa_circ_127736,RMVar_hsa_circ_294558,RMVar_hsa_circ_236282 8576 RMVar_ID_8576 Human_SNP_ID_261866297 A-to-I Human chr5 + 172999423 172999423 172999423 ATAGTTCACTGCAGCCTCAAACTCCTGGGCTGAAGCAATCTTCCTGCCTCAGCCTCCTGAGTAGC ATAGTTCACTGCAGCCTCAAACTCCTGGGCTGGAGCAATCTTCCTGCCTCAGCCTCCTGAGTAGC A G ATP6V0E1 Ensembl:ENSG00000113732 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1455034398 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122921,RMVar_hsa_circ_236281,RMVar_hsa_circ_127736,RMVar_hsa_circ_294558,RMVar_hsa_circ_236282 8577 RMVar_ID_8577 Human_SNP_ID_261866307 A-to-I Human chr5 + 172999463 172999463 172999463 TTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGACATACACCACCACACCTGGCTAATTTTT TTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTGCAGACATACACCACCACACCTGGCTAATTTTT A G ATP6V0E1 Ensembl:ENSG00000113732 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965245481 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122921,RMVar_hsa_circ_236281,RMVar_hsa_circ_127736,RMVar_hsa_circ_294558,RMVar_hsa_circ_236282 8578 RMVar_ID_8578 Human_SNP_ID_261866717 A-to-I Human chr5 + 173001346 173001346 173001346 TTCACTTCCCAAACAGGTTCCCCCATCCACTCATTTCCACAAATACCTACTCAGTTATGACCTCA TTCACTTCCCAAACAGGTTCCCCCATCCACTCGTTTCCACAAATACCTACTCAGTTATGACCTCA A G ATP6V0E1 Ensembl:ENSG00000113732 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs565130176 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122921,RMVar_hsa_circ_236281,RMVar_hsa_circ_127736,RMVar_hsa_circ_294558,RMVar_hsa_circ_236282 8579 RMVar_ID_8579 Human_SNP_ID_261866718 A-to-I Human chr5 + 173001346 173001346 173001346 TTCACTTCCCAAACAGGTTCCCCCATCCACTCATTTCCACAAATACCTACTCAGTTATGACCTCA TTCACTTCCCAAACAGGTTCCCCCATCCACTCTTTTCCACAAATACCTACTCAGTTATGACCTCA A T ATP6V0E1 Ensembl:ENSG00000113732 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs565130176 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122921,RMVar_hsa_circ_236281,RMVar_hsa_circ_127736,RMVar_hsa_circ_294558,RMVar_hsa_circ_236282 8580 RMVar_ID_8580 Human_SNP_ID_261866720 A-to-I Human chr5 + 173001354 173001354 173001354 CCAAACAGGTTCCCCCATCCACTCATTTCCACAAATACCTACTCAGTTATGACCTCAGAAGATTC CCAAACAGGTTCCCCCATCCACTCATTTCCACCAATACCTACTCAGTTATGACCTCAGAAGATTC A C ATP6V0E1 Ensembl:ENSG00000113732 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1422999273 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122921,RMVar_hsa_circ_236281,RMVar_hsa_circ_127736,RMVar_hsa_circ_294558,RMVar_hsa_circ_236282 8581 RMVar_ID_8581 Human_SNP_ID_261869187 A-to-I Human chr5 + 173012215 173012215 173012215 TACTGTGCCTGGCTGATTTTTATATTTTTAGTAGAGATAGTGTTTCCCCATATTGGCCAGGCTGG TACTGTGCCTGGCTGATTTTTATATTTTTAGTTGAGATAGTGTTTCCCCATATTGGCCAGGCTGG A T ATP6V0E1 Ensembl:ENSG00000113732 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1451299598 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122921,RMVar_hsa_circ_236281,RMVar_hsa_circ_127736,RMVar_hsa_circ_294558,RMVar_hsa_circ_236282 8582 RMVar_ID_8582 Human_SNP_ID_261870852 A-to-I Human chr5 + 173018987 173018987 173018987 TTTTTCTTTTCTTTTTTTAGAGACAGGGTCTCACTCTGTTGCCCAGGCTGGAGTGCAGTGATGTA TTTTTCTTTTCTTTTTTTAGAGACAGGGTCTCCCTCTGTTGCCCAGGCTGGAGTGCAGTGATGTA A C ATP6V0E1 Ensembl:ENSG00000113732 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947237282 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122921,RMVar_hsa_circ_236281,RMVar_hsa_circ_127736,RMVar_hsa_circ_294558,RMVar_hsa_circ_236282 8583 RMVar_ID_8583 Human_SNP_ID_261871821 A-to-I Human chr5 + 173022543 173022543 173022543 TTCTTGTCACCTAGGCTGGAGTACAGTTGCACAATCACGGCTAACTGCAGTCTTGACCTCCTGGG TTCTTGTCACCTAGGCTGGAGTACAGTTGCACCATCACGGCTAACTGCAGTCTTGACCTCCTGGG A C ATP6V0E1 Ensembl:ENSG00000113732 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1245908689 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15383027 RMVar_hsa_circ_122921,RMVar_hsa_circ_236281,RMVar_hsa_circ_127736,RMVar_hsa_circ_118646,RMVar_hsa_circ_236282,RMVar_hsa_circ_236283 8584 RMVar_ID_8584 Human_SNP_ID_261872068 A-to-I Human chr5 + 173023686 173023686 173023686 GGGCAATATTGTGAAACCTTGTCTCTACAAAAAATACAAAAATTAGCCAGGCAAGGTGGTGCACA GGGCAATATTGTGAAACCTTGTCTCTACAAAAGATACAAAAATTAGCCAGGCAAGGTGGTGCACA A G ATP6V0E1 Ensembl:ENSG00000113732 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1267551831 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122921,RMVar_hsa_circ_236281,RMVar_hsa_circ_127736,RMVar_hsa_circ_118646,RMVar_hsa_circ_236282,RMVar_hsa_circ_236283 8585 RMVar_ID_8585 Human_SNP_ID_261872665 A-to-I Human chr5 + 173025607 173025607 173025607 ACCTCTGCCTCCTGGGCTCAAGTGATCCTCCTACCTCAGCCTTCTGATTATCTGGGACTGTAGAC ACCTCTGCCTCCTGGGCTCAAGTGATCCTCCTGCCTCAGCCTTCTGATTATCTGGGACTGTAGAC A G ATP6V0E1 Ensembl:ENSG00000113732 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs748353544 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122921,RMVar_hsa_circ_236281,RMVar_hsa_circ_127736,RMVar_hsa_circ_118646,RMVar_hsa_circ_236282,RMVar_hsa_circ_236283 8586 RMVar_ID_8586 Human_SNP_ID_261873005 A-to-I Human chr5 + 173027085 173027085 173027085 CCTGTAGTCCCAGCTACTCGGGAGGCTGGGGCAGGATAATGGCATGAACCTGGGAGGCGGAGCTT CCTGTAGTCCCAGCTACTCGGGAGGCTGGGGCGGGATAATGGCATGAACCTGGGAGGCGGAGCTT A G ATP6V0E1 Ensembl:ENSG00000113732 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs763476921 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122921,RMVar_hsa_circ_236281,RMVar_hsa_circ_127736,RMVar_hsa_circ_118646,RMVar_hsa_circ_236282,RMVar_hsa_circ_236283 8587 RMVar_ID_8587 Human_SNP_ID_261873834 A-to-I Human chr5 + 173030558 173030558 173030558 CGCCTCCTGGGTTCAAGTGATTCTCGTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGAATGTG CGCCTCCTGGGTTCAAGTGATTCTCGTGCCTCGGCCTCCCGAGTAGCTGGGATTACAGGAATGTG A G ATP6V0E1 Ensembl:ENSG00000113732 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs970721420 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122921,RMVar_hsa_circ_236281,RMVar_hsa_circ_127736,RMVar_hsa_circ_118646,RMVar_hsa_circ_236282,RMVar_hsa_circ_236283 8588 RMVar_ID_8588 Human_SNP_ID_261874075 A-to-I Human chr5 + 173031284 173031284 173031284 GTATTTTTTTTTTAGTAGAGATGGGGTACATCATGTTGTCCAGGCTGTTCTCGAACTCCTGACCT GTATTTTTTTTTTAGTAGAGATGGGGTACATCGTGTTGTCCAGGCTGTTCTCGAACTCCTGACCT A G ATP6V0E1 Ensembl:ENSG00000113732 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1397332600 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15383190 RMVar_hsa_circ_122921,RMVar_hsa_circ_236281,RMVar_hsa_circ_127736,RMVar_hsa_circ_118646,RMVar_hsa_circ_236282,RMVar_hsa_circ_236283 8589 RMVar_ID_8589 Human_SNP_ID_261874301 A-to-I Human chr5 + 173032015 173032015 173032015 ACAACAACAAAAAATACAAAAATCAGCCAGGTATGGTGGCACACGCCTGTAGTCCTAGCTACTTG ACAACAACAAAAAATACAAAAATCAGCCAGGTTTGGTGGCACACGCCTGTAGTCCTAGCTACTTG A T ATP6V0E1 Ensembl:ENSG00000113732 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1245128629 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122921,RMVar_hsa_circ_236281,RMVar_hsa_circ_127736,RMVar_hsa_circ_118646,RMVar_hsa_circ_236282,RMVar_hsa_circ_236283 8590 RMVar_ID_8590 Human_SNP_ID_261874468 A-to-I Human chr5 + 173032362 173032362 173032362 CAGGCTGGAGTCCAATGGTGTGATCTCAGCTCACTGCAACCTCCGCCTCCTGGGTTCAAGCCATT CAGGCTGGAGTCCAATGGTGTGATCTCAGCTCGCTGCAACCTCCGCCTCCTGGGTTCAAGCCATT A G ATP6V0E1 Ensembl:ENSG00000113732 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs191023924 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122921,RMVar_hsa_circ_236281,RMVar_hsa_circ_127736,RMVar_hsa_circ_118646,RMVar_hsa_circ_236282,RMVar_hsa_circ_236283 8591 RMVar_ID_8591 Human_SNP_ID_261902989 A-to-I Human chr5 + 173147294 173147294 173147294 GGGCATGGTGGCAGGTGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATGGCGTGAA GGGCATGGTGGCAGGTGCCTGTAGTCCCAGCTGCTCAGGAGGCTGAGGCAGGAGAATGGCGTGAA A G BNIP1 Ensembl:ENSG00000113734 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1444119973 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18568 8592 RMVar_ID_8592 Human_SNP_ID_262016020 A-to-I Human chr5 - 173608071 173608071 173608071 TGCATTGTGCTGCCATTTGGCCAGCCTGTCCAAGGGCATGACACCAAGTAGACACTACAGAGAGA TGCATTGTGCTGCCATTTGGCCAGCCTGTCCACGGGCATGACACCAAGTAGACACTACAGAGAGA T G BOD1 Ensembl:ENSG00000145919 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1303874827 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_637976,Human_RBP_ID_5121467,Human_RBP_ID_15385592,Human_RBP_ID_17299512,Human_RBP_ID_22099832,Human_RBP_ID_24097385 Human_miRNA_ID_594703,Human_miRNA_ID_1271408 8593 RMVar_ID_8593 Human_SNP_ID_262043801 A-to-I Human chr5 - 173717332 173717330 173717332 TGTATAAATGCATAGACCTATGTGATTATCATATGTTTTATGCATTGTTATGAGTGCAAGCTACT TGTATAAATGCATAGACCTATGTGATTATCAT__GTTTTATGCATTGTTATGAGTGCAAGCTACT CAT C LINC01484 Ensembl:ENSG00000253686 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs952834743 Functional Loss DEL dbSNP153 33..34 33 - - - 8594 RMVar_ID_8594 Human_SNP_ID_262047760 A-to-I Human chr5 - 173732186 173732186 173732186 TCTCAGCTTACTGTAGCCTCTACATGAGGATCAGGTGATCCTCCCACCTCAGCCTCCTGAGTAGC TCTCAGCTTACTGTAGCCTCTACATGAGGATCGGGTGATCCTCCCACCTCAGCCTCCTGAGTAGC T C LINC01484 Ensembl:ENSG00000253686 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1013274794 Functional Loss SNV dbSNP153 33..33 33 - - - 8595 RMVar_ID_8595 Human_SNP_ID_262049712 A-to-I Human chr5 - 173739165 173739165 173739165 TCGGCTCACTGAACCTCCGCCTCCTGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGCT TCGGCTCACTGAACCTCCGCCTCCTGGGTTCAGGTGATTCTCCTGCCTCAGCCTCCCAAGTAGCT T C LINC01484 Ensembl:ENSG00000253686 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs914613957 Functional Loss SNV dbSNP153 33..33 33 - - - 8596 RMVar_ID_8596 Human_SNP_ID_262089530 A-to-I Human chr5 + 173894093 173894093 173894093 CAGCTCACTGCAGCCTTGACCTCCCTGGGCTCAAGAGATCCTCCTGCCTCAGCTTCCCCAGTAGC CAGCTCACTGCAGCCTTGACCTCCCTGGGCTCGAGAGATCCTCCTGCCTCAGCTTCCCCAGTAGC A G CPEB4 Ensembl:ENSG00000113742 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1049825919 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_236297,RMVar_hsa_circ_103933 8597 RMVar_ID_8597 Human_SNP_ID_262097129 A-to-I Human chr5 + 173930124 173930124 173930124 TCTCCCAGGCTGGAGAGCAGTGGCGAGATCTCAGCTCACTGCAACCCCTGCCTCCTGGATTCAAG TCTCCCAGGCTGGAGAGCAGTGGCGAGATCTCGGCTCACTGCAACCCCTGCCTCCTGGATTCAAG A G CPEB4 Ensembl:ENSG00000113742 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1165506794 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71257,RMVar_hsa_circ_236297,RMVar_hsa_circ_103933,RMVar_hsa_circ_311433,RMVar_hsa_circ_334639,RMVar_hsa_circ_236299,RMVar_hsa_circ_38068,RMVar_hsa_circ_236300 8598 RMVar_ID_8598 Human_SNP_ID_262100726 A-to-I Human chr5 + 173946920 173946920 173946920 TATTCCAAACTGGAATATCACCATAATGGTGCAATACCATCCTGTCCTACCATGCGCATGTTAAC TATTCCAAACTGGAATATCACCATAATGGTGCCATACCATCCTGTCCTACCATGCGCATGTTAAC A C CPEB4 Ensembl:ENSG00000113742 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1034096629 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59669,RMVar_hsa_circ_236297,RMVar_hsa_circ_103933,RMVar_hsa_circ_311433,RMVar_hsa_circ_38068,RMVar_hsa_circ_236300,RMVar_hsa_circ_298678,RMVar_hsa_circ_236304,RMVar_hsa_circ_236302,RMVar_hsa_circ_236301,RMVar_hsa_circ_341151,RMVar_hsa_circ_124180,RMVar_hsa_circ_287027,RMVar_hsa_circ_308763,RMVar_hsa_circ_236305,RMVar_hsa_circ_236303 8599 RMVar_ID_8599 Human_SNP_ID_262111913 A-to-I Human chr5 + 173993533 173993533 173993533 TGTGGTGGTGCGCGCCTGCTGTAATCCCAGCTACTGGGGAGGCTGAGTCAGGAGAATGGCTTGAA TGTGGTGGTGCGCGCCTGCTGTAATCCCAGCTGCTGGGGAGGCTGAGTCAGGAGAATGGCTTGAA A G C5orf47 Ensembl:ENSG00000185056 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1374507464 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_236308,RMVar_hsa_circ_368511 8600 RMVar_ID_8600 Human_SNP_ID_262492339 A-to-I Human chr5 + 175496953 175496953 175496953 TTGCTCGGTCACCCAGGCTAGAGTGCAGTGGCACACCAGCTCACTGTAACCTCTGCCTCCCGGGT TTGCTCGGTCACCCAGGCTAGAGTGCAGTGGCGCACCAGCTCACTGTAACCTCTGCCTCCCGGGT A G SFXN1 Ensembl:ENSG00000164466 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1294275006 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92872,RMVar_hsa_circ_17586,RMVar_hsa_circ_236314,RMVar_hsa_circ_300266,RMVar_hsa_circ_54925,RMVar_hsa_circ_236315,RMVar_hsa_circ_12696 8601 RMVar_ID_8601 Human_SNP_ID_262500578 A-to-I Human chr5 + 175527999 175527999 175527999 TGGAGTGCAGTGGCGTAGTCTCGGCTCACTGCAAGCTCCGCCTCCCGGGTTCACGCCGTTCTCCT TGGAGTGCAGTGGCGTAGTCTCGGCTCACTGCCAGCTCCGCCTCCCGGGTTCACGCCGTTCTCCT A C SFXN1 Ensembl:ENSG00000164466 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1321926577 Functional Loss SNV dbSNP153 33..33 33 - - - 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 8602 RMVar_ID_8602 Human_SNP_ID_262500596 A-to-I Human chr5 + 175528049 175528049 175528049 TCACGCCGTTCTCCTGCCTCAGCCTCTCTGAGAAGCTGGGACTACAGGCGCCCGCCACCACGCCC TCACGCCGTTCTCCTGCCTCAGCCTCTCTGAGTAGCTGGGACTACAGGCGCCCGCCACCACGCCC A T SFXN1 Ensembl:ENSG00000164466 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1316320511 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_638139,Human_RBP_ID_15387354 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 8603 RMVar_ID_8603 Human_SNP_ID_262500616 A-to-I Human chr5 + 175528086 175528086 175528086 GGGACTACAGGCGCCCGCCACCACGCCCGGCTAATTTTTTTGTATTTTTAGTAGAGACGGGGTTT GGGACTACAGGCGCCCGCCACCACGCCCGGCTCATTTTTTTGTATTTTTAGTAGAGACGGGGTTT A C SFXN1 Ensembl:ENSG00000164466 Protein coding 3'UTR GSE38233;GSE100210;GSE99789 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 24183664,29129909,29796672 RNA-Seq:(High) rs1203238283 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_165701 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 8604 RMVar_ID_8604 Human_SNP_ID_262500617 A-to-I Human chr5 + 175528086 175528086 175528086 GGGACTACAGGCGCCCGCCACCACGCCCGGCTAATTTTTTTGTATTTTTAGTAGAGACGGGGTTT GGGACTACAGGCGCCCGCCACCACGCCCGGCTGATTTTTTTGTATTTTTAGTAGAGACGGGGTTT A G SFXN1 Ensembl:ENSG00000164466 Protein coding 3'UTR GSE38233;GSE100210;GSE99789 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 24183664,29129909,29796672 RNA-Seq:(High) rs1203238283 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_165701 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 8605 RMVar_ID_8605 Human_SNP_ID_262500886 A-to-I Human chr5 + 175529081 175529081 175529081 AGGAATGGCCGGGTGCGGTGGCTCACCCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGTGG AGGAATGGCCGGGTGCGGTGGCTCACCCCTGTGATCCCAGCACTTTGGGAGGCCGAGGCGGGTGG A G SFXN1 Ensembl:ENSG00000164466 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1235275464 Functional Loss SNV dbSNP153 33..33 33 - - - 8606 RMVar_ID_8606 Human_SNP_ID_262500913 A-to-I Human chr5 + 175529175 175529175 175529175 CCTGGCCAACATGGAGAAACCCCGCCTCTACTAAAAATACAAAAAATTAGCCAGGCATGGAGGCA CCTGGCCAACATGGAGAAACCCCGCCTCTACTGAAAATACAAAAAATTAGCCAGGCATGGAGGCA A G SFXN1 Ensembl:ENSG00000164466 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1354724206 Functional Loss SNV dbSNP153 33..33 33 - - - 8607 RMVar_ID_8607 Human_SNP_ID_262500928 A-to-I Human chr5 + 175529215 175529215 175529215 AAAAAATTAGCCAGGCATGGAGGCACATGCCTATAATCCCAGCTACTCGGGAGGCTGAGGTAGGA AAAAAATTAGCCAGGCATGGAGGCACATGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGTAGGA A G SFXN1 Ensembl:ENSG00000164466 Protein coding 3'UTR GSE38233;GSE107867 cultured B-cells;ASD brains,Fragile X samples from NIH NeuroBioBank - 24183664,30559470 RNA-Seq:(High) rs1294012927 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4852952 8608 RMVar_ID_8608 Human_SNP_ID_262500929 A-to-I Human chr5 + 175529217 175529217 175529217 AAAATTAGCCAGGCATGGAGGCACATGCCTATAATCCCAGCTACTCGGGAGGCTGAGGTAGGAGA AAAATTAGCCAGGCATGGAGGCACATGCCTATGATCCCAGCTACTCGGGAGGCTGAGGTAGGAGA A G SFXN1 Ensembl:ENSG00000164466 Protein coding 3'UTR GSE38233;GSE100210;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 24183664,29129909,30559470 RNA-Seq:(High) rs1334186887 Functional Loss SNV dbSNP153 33..33 33 - - - 8609 RMVar_ID_8609 Human_SNP_ID_262500966 A-to-I Human chr5 + 175529334 175529334 175529334 CACTCCAGCCTGGGCAACAAGAGCGAAACTCCATCTCAAAAAAAAAAAAAAGAGATTATAAAAGG CACTCCAGCCTGGGCAACAAGAGCGAAACTCCGTCTCAAAAAAAAAAAAAAGAGATTATAAAAGG A G SFXN1 Ensembl:ENSG00000164466 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1369049814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_638163 Human_miRNA_ID_186255,Human_miRNA_ID_302955,Human_miRNA_ID_1120043,Human_miRNA_ID_1127193,Human_miRNA_ID_1382556 8610 RMVar_ID_8610 Human_SNP_ID_262542859 A-to-I Human chr5 + 175700875 175700875 175700875 GTGCCACTGCACTCCAGCCTGGGCGACAGAGCAAGACTCTGTCTCAAAAAAAAGAAAAGAAAAGA GTGCCACTGCACTCCAGCCTGGGCGACAGAGCGAGACTCTGTCTCAAAAAAAAGAAAAGAAAAGA A G HRH2 Ensembl:ENSG00000113749 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs754634837 Functional Loss SNV dbSNP153 33..33 33 - - - 8611 RMVar_ID_8611 Human_SNP_ID_262594658 A-to-I Human chr5 - 175920289 175920289 175920289 AAAGTGCTATGATGCGATCTCGACTCATCACAACCTCCGCCTCCTGGGTTCCAGTGATTCTTCTG AAAGTGCTATGATGCGATCTCGACTCATCACAGCCTCCGCCTCCTGGGTTCCAGTGATTCTTCTG T C AC138965.2,THOC3 Ensembl:ENSG00000250820,Ensembl:ENSG00000051596 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1393170094 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7419033 8612 RMVar_ID_8612 Human_SNP_ID_262599588 A-to-I Human chr5 - 175934917 175934917 175934917 AAACCCTGTCTCTACTGAAAATACAAAATATTAGCCAGACGTGGTGGCGGGTGCCTGTAATCCCA AAACCCTGTCTCTACTGAAAATACAAAATATTCGCCAGACGTGGTGGCGGGTGCCTGTAATCCCA T G AC138965.2,THOC3 Ensembl:ENSG00000250820,Ensembl:ENSG00000051596 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1310347902 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8269209,Human_RBP_ID_25880792 8613 RMVar_ID_8613 Human_SNP_ID_262636538 A-to-I Human chr5 + 176093755 176093755 176093755 ATTTATTTTCTGTCGTTACAGACATCCTTGGGAGTTCCACAATGTGGTACGTATTGGGGAACCCC ATTTATTTTCTGTCGTTACAGACATCCTTGGGCGTTCCACAATGTGGTACGTATTGGGGAACCCC A C AC139491.7,FAM153B Ensembl:ENSG00000285476,Ensembl:ENSG00000182230 Protein coding,Protein coding CDS,CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs756424964 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_Splice_Rec_722244,Human_Splice_Rec_722245,Human_Splice_Rec_722342,Human_Splice_Rec_722343,Human_Splice_Rec_722386,Human_Splice_Rec_722387,Human_Splice_Rec_722416,Human_Splice_Rec_722417,Human_Splice_Rec_722448,Human_Splice_Rec_722449,Human_Splice_Rec_722464,Human_Splice_Rec_722465,Human_Splice_Rec_722508,Human_Splice_Rec_722509 8614 RMVar_ID_8614 Human_SNP_ID_262636540 A-to-I Human chr5 - 176093765 176093765 176093765 CAGTATGAGAGGGGTTCCCCAATACGTACCACATTGTGGAACTCCCAAGGATGTCTGTAACGACA CAGTATGAGAGGGGTTCCCCAATACGTACCACGTTGTGGAACTCCCAAGGATGTCTGTAACGACA T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1335162051 Functional Loss SNV dbSNP153 33..33 33 - - - 8615 RMVar_ID_8615 Human_SNP_ID_262643365 A-to-I Human chr5 + 176120936 176120936 176120936 TTCTCATGGCTCATACTCGTCTGAAACGACTCAGGTAGAGGCTGAGGAAGGCCGTGTTGTTTGTC TTCTCATGGCTCATACTCGTCTGAAACGACTCGGGTAGAGGCTGAGGAAGGCCGTGTTGTTTGTC A G AC139491.7,AC139491.5 Ensembl:ENSG00000285476,Ensembl:ENSG00000251623 Protein coding,Pseudogene 3'UTR,exon GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1212710216 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_722546,Human_Splice_Rec_722547,Human_Splice_Rec_722556,Human_Splice_Rec_722557,Human_Splice_Rec_722562,Human_Splice_Rec_722563,Human_Splice_Rec_722572,Human_Splice_Rec_722573,Human_Splice_Rec_722588,Human_Splice_Rec_722589,Human_Splice_Rec_722591 RMVar_hsa_circ_360053 8616 RMVar_ID_8616 Human_SNP_ID_262680737 A-to-I Human chr5 + 176261760 176261759 176261760 ACAGAGCAAGACTCTGTCTCAAAAAAAAAAGGAAAAAAAAAAGTTTTATGAATAAGTAATTTAAG ACAGAGCAAGACTCTGTCTCAAAAAAAAAAGG_AAAAAAAAAGTTTTATGAATAAGTAATTTAAG GA G SIMC1 Ensembl:ENSG00000170085 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1340857291 Functional Loss DEL dbSNP153 33..33 33 - - - 8617 RMVar_ID_8617 Human_SNP_ID_262680739 A-to-I Human chr5 + 176261760 176261760 176261760 ACAGAGCAAGACTCTGTCTCAAAAAAAAAAGGAAAAAAAAAAGTTTTATGAATAAGTAATTTAAG ACAGAGCAAGACTCTGTCTCAAAAAAAAAAGGGAAAAAAAAAGTTTTATGAATAAGTAATTTAAG A G SIMC1 Ensembl:ENSG00000170085 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1413213781 Functional Loss SNV dbSNP153 33..33 33 - - - 8618 RMVar_ID_8618 Human_SNP_ID_262694303 A-to-I Human chr5 + 176308801 176308801 176308801 CCCAAGATCCTGTGCCAGGAGGAGCAGGATGCATATTGGAGGATCCACAGCCTTACACATCTGGA CCCAAGATCCTGTGCCAGGAGGAGCAGGATGCCTATTGGAGGATCCACAGCCTTACACATCTGGA A C BRCC3P1,SIMC1 Ensembl:ENSG00000251667,Ensembl:ENSG00000170085 Pseudogene,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs529194638 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18838746 RMVar_hsa_circ_58004,RMVar_hsa_circ_63765,RMVar_hsa_circ_306548,RMVar_hsa_circ_309390,RMVar_hsa_circ_236342,RMVar_hsa_circ_322535 8619 RMVar_ID_8619 Human_SNP_ID_262694304 A-to-I Human chr5 + 176308801 176308801 176308801 CCCAAGATCCTGTGCCAGGAGGAGCAGGATGCATATTGGAGGATCCACAGCCTTACACATCTGGA CCCAAGATCCTGTGCCAGGAGGAGCAGGATGCGTATTGGAGGATCCACAGCCTTACACATCTGGA A G BRCC3P1,SIMC1 Ensembl:ENSG00000251667,Ensembl:ENSG00000170085 Pseudogene,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs529194638 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18838746 RMVar_hsa_circ_58004,RMVar_hsa_circ_63765,RMVar_hsa_circ_306548,RMVar_hsa_circ_309390,RMVar_hsa_circ_236342,RMVar_hsa_circ_322535 8620 RMVar_ID_8620 Human_SNP_ID_262703864 A-to-I Human chr5 - 176349557 176349557 176349557 GTGATCCTCCCAACTCAGCCTCCCAAATAGCTAGGATTTACAGGCATGCGCCACCATGCCCAGCT GTGATCCTCCCAACTCAGCCTCCCAAATAGCTGGGATTTACAGGCATGCGCCACCATGCCCAGCT T C KIAA1191 Ensembl:ENSG00000122203 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs952177644 Functional Loss SNV dbSNP153 33..33 33 - - - 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 8621 RMVar_ID_8621 Human_SNP_ID_262705456 A-to-I Human chr5 - 176356066 176356066 176356066 CAACTACTCGCTAGGCTGAGGCACTTGAGCCCAGGAGGTTGAGCCTGCAGTGAGCCGTGATCGTG CAACTACTCGCTAGGCTGAGGCACTTGAGCCCGGGAGGTTGAGCCTGCAGTGAGCCGTGATCGTG T C KIAA1191 Ensembl:ENSG00000122203 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs905759113 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250044,Human_RBP_ID_15389635 RMVar_hsa_circ_14792,RMVar_hsa_circ_236358,RMVar_hsa_circ_112696,RMVar_hsa_circ_236360,RMVar_hsa_circ_370777 8622 RMVar_ID_8622 Human_SNP_ID_262709070 A-to-I Human chr5 + 176369772 176369772 176369772 GATTCCAGGAGTTCGAGACCAGCCTGGGCAACATGGTGAAACTCCGTCTCTACAAAAAAAATGCA GATTCCAGGAGTTCGAGACCAGCCTGGGCAACGTGGTGAAACTCCGTCTCTACAAAAAAAATGCA A G ARL10 Ensembl:ENSG00000175414 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs923244567 Functional Loss SNV dbSNP153 33..33 33 - - - 8623 RMVar_ID_8623 Human_SNP_ID_262709086 A-to-I Human chr5 + 176369874 176369874 176369874 CCAGCTACTTTAGAGGCTGAGGCAGAAAGATCACTTGAACCCAGGAGGTCGAGGCTGCAGTGAGC CCAGCTACTTTAGAGGCTGAGGCAGAAAGATCTCTTGAACCCAGGAGGTCGAGGCTGCAGTGAGC A T ARL10 Ensembl:ENSG00000175414 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1378916454 Functional Loss SNV dbSNP153 33..33 33 - - - 8624 RMVar_ID_8624 Human_SNP_ID_262709513 A-to-I Human chr5 + 176371332 176371332 176371332 TCCACCACAGGAGGTGGAGGTTGCAGTGAGCCAAGATCGTGCCACTGCACTCCAGCCTGGGTGAC TCCACCACAGGAGGTGGAGGTTGCAGTGAGCCGAGATCGTGCCACTGCACTCCAGCCTGGGTGAC A G ARL10 Ensembl:ENSG00000175414 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs954911361 Functional Loss SNV dbSNP153 33..33 33 - - - 8625 RMVar_ID_8625 Human_SNP_ID_262710886 A-to-I Human chr5 + 176376205 176376205 176376205 AACACAGTGAAACCCTGTCTCTACTATAAAATACAAAAAATCAGCTGGGTGTGACGGCATGCGCC AACACAGTGAAACCCTGTCTCTACTATAAAATGCAAAAAATCAGCTGGGTGTGACGGCATGCGCC A G ARL10 Ensembl:ENSG00000175414 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs550935780 Functional Loss SNV dbSNP153 33..33 33 - - - 8626 RMVar_ID_8626 Human_SNP_ID_262710892 A-to-I Human chr5 + 176376231 176376231 176376231 TAAAATACAAAAAATCAGCTGGGTGTGACGGCATGCGCCTGTAGTCCCACCTACTAGGGAGGCTG TAAAATACAAAAAATCAGCTGGGTGTGACGGCTTGCGCCTGTAGTCCCACCTACTAGGGAGGCTG A T ARL10 Ensembl:ENSG00000175414 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1191514505 Functional Loss SNV dbSNP153 33..33 33 - - - 8627 RMVar_ID_8627 Human_SNP_ID_262710899 A-to-I Human chr5 + 176376241 176376241 176376241 AAAATCAGCTGGGTGTGACGGCATGCGCCTGTAGTCCCACCTACTAGGGAGGCTGAGGCATGAGA AAAATCAGCTGGGTGTGACGGCATGCGCCTGTGGTCCCACCTACTAGGGAGGCTGAGGCATGAGA A G ARL10 Ensembl:ENSG00000175414 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs181709804 Functional Loss SNV dbSNP153 33..33 33 - - - 8628 RMVar_ID_8628 Human_SNP_ID_262710907 A-to-I Human chr5 + 176376281 176376281 176376281 CTACTAGGGAGGCTGAGGCATGAGAATCACTTAAACTTGGGAGGCAGAGGTTGCAGTGAGCTGAG CTACTAGGGAGGCTGAGGCATGAGAATCACTTTAACTTGGGAGGCAGAGGTTGCAGTGAGCTGAG A T ARL10 Ensembl:ENSG00000175414 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs979522754 Functional Loss SNV dbSNP153 33..33 33 - - - 8629 RMVar_ID_8629 Human_SNP_ID_262710916 A-to-I Human chr5 + 176376317 176376317 176376317 TTGGGAGGCAGAGGTTGCAGTGAGCTGAGATCACGTCACTGCACTCTAGCCTGGGAGACAGAGCG TTGGGAGGCAGAGGTTGCAGTGAGCTGAGATCCCGTCACTGCACTCTAGCCTGGGAGACAGAGCG A C ARL10 Ensembl:ENSG00000175414 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1378020762 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25881106 8630 RMVar_ID_8630 Human_SNP_ID_262713579 A-to-I Human chr5 - 176387217 176387217 176387217 AATTTAGCTGGGCATGGTGGCGCATGATTGTAATCCCAGCTACTTGAGAGGCTGAGGCAGGAGAT AATTTAGCTGGGCATGGTGGCGCATGATTGTAGTCCCAGCTACTTGAGAGGCTGAGGCAGGAGAT T C NOP16 Ensembl:ENSG00000048162 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs374646842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17575587 RMVar_hsa_circ_236365,RMVar_hsa_circ_309799 8631 RMVar_ID_8631 Human_SNP_ID_262713687 A-to-I Human chr5 - 176387739 176387739 176387739 TGCCACCATACCCGGCTGATTTTTGTGGTTTTAGTAGAGGCAGGGTTTCGCTATGTTGGCCAGGC TGCCACCATACCCGGCTGATTTTTGTGGTTTTGGTAGAGGCAGGGTTTCGCTATGTTGGCCAGGC T C NOP16 Ensembl:ENSG00000048162 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs549195963 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17575588 RMVar_hsa_circ_236365,RMVar_hsa_circ_309799 8632 RMVar_ID_8632 Human_SNP_ID_262714007 A-to-I Human chr5 - 176388711 176388711 176388711 AACGAATAAATTGAGCCTTGTACGCAGGCGCAAATGCTCGTTGCATCCTGGGAGTCGTAGTGCTC AACGAATAAATTGAGCCTTGTACGCAGGCGCATATGCTCGTTGCATCCTGGGAGTCGTAGTGCTC T A NOP16 Ensembl:ENSG00000048162 Protein coding 5'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs569953100 Functional Loss SNV dbSNP153 33..33 33 - - - 8633 RMVar_ID_8633 Human_SNP_ID_262714008 A-to-I Human chr5 - 176388711 176388711 176388711 AACGAATAAATTGAGCCTTGTACGCAGGCGCAAATGCTCGTTGCATCCTGGGAGTCGTAGTGCTC AACGAATAAATTGAGCCTTGTACGCAGGCGCAGATGCTCGTTGCATCCTGGGAGTCGTAGTGCTC T C NOP16 Ensembl:ENSG00000048162 Protein coding 5'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs569953100 Functional Loss SNV dbSNP153 33..33 33 - - - 8634 RMVar_ID_8634 Human_SNP_ID_262714720 A-to-I Human chr5 - 176390684 176390684 176390684 CCAGCACTTTGGGAGGCCGAGGTTGGGGGATTACCTGAGGTCAGGAGTTCAAGACCAGCCTGGCC CCAGCACTTTGGGAGGCCGAGGTTGGGGGATTGCCTGAGGTCAGGAGTTCAAGACCAGCCTGGCC T C RF00017-049 RNACentral:URS000096B6E3 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1331147590 Functional Loss SNV dbSNP153 33..33 33 - - - 8635 RMVar_ID_8635 Human_SNP_ID_262717270 A-to-I Human chr5 - 176400108 176400108 176400108 ACTGCAGCCTCCCCTGCCCCGCCCCGGATTCAAGTGATTCTTGTGCCTCAGCCTCCCGAGTAGGT ACTGCAGCCTCCCCTGCCCCGCCCCGGATTCAGGTGATTCTTGTGCCTCAGCCTCCCGAGTAGGT T C CLTB Ensembl:ENSG00000175416 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs542715747 Functional Loss SNV dbSNP153 33..33 33 - - - 8636 RMVar_ID_8636 Human_SNP_ID_262719126 A-to-I Human chr5 - 176407455 176407455 176407455 TACTAAAAATACAAAAATTGGCTAGGCAGGGTAGTGGTTGCCTGTAATCCCAGCTACTCAGGAGG TACTAAAAATACAAAAATTGGCTAGGCAGGGTGGTGGTTGCCTGTAATCCCAGCTACTCAGGAGG T C CLTB Ensembl:ENSG00000175416 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1162749750 Functional Loss SNV dbSNP153 33..33 33 - - - 8637 RMVar_ID_8637 Human_SNP_ID_262729825 A-to-I Human chr5 + 176449299 176449299 176449299 AGGACTGTCTTAAAAATGTCTACCCCCAGGCCAGGAGCGGTGGCTCACGCCTGTAATCCCAGCAC AGGACTGTCTTAAAAATGTCTACCCCCAGGCCGGGAGCGGTGGCTCACGCCTGTAATCCCAGCAC A G FAF2 Ensembl:ENSG00000113194 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1300209926 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23258918 RMVar_hsa_circ_110296,RMVar_hsa_circ_236370 8638 RMVar_ID_8638 Human_SNP_ID_262730857 A-to-I Human chr5 + 176452319 176452319 176452319 ACCTCAGGTGATCCACCTGCCTCGGCCTCCCAAAGTGCTCGGATTACAGGCGTGAGCCACCGGAC ACCTCAGGTGATCCACCTGCCTCGGCCTCCCAGAGTGCTCGGATTACAGGCGTGAGCCACCGGAC A G FAF2 Ensembl:ENSG00000113194 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1229637737 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110296,RMVar_hsa_circ_236370 8639 RMVar_ID_8639 Human_SNP_ID_262734032 A-to-I Human chr5 + 176464592 176464592 176464592 ATAGCTCACTGTAGCCTCGACCTCCCGGACTCAAGTGACCCTCCCACATCAGCCTCCCAAGTGGC ATAGCTCACTGTAGCCTCGACCTCCCGGACTCCAGTGACCCTCCCACATCAGCCTCCCAAGTGGC A C FAF2 Ensembl:ENSG00000113194 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs952518644 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15390640 RMVar_hsa_circ_110296,RMVar_hsa_circ_236370 8640 RMVar_ID_8640 Human_SNP_ID_262734045 A-to-I Human chr5 + 176464632 176464632 176464632 CTCCCACATCAGCCTCCCAAGTGGCTGGGACTACATGCATGTACCACCATGCCCGGCTAATGTTT CTCCCACATCAGCCTCCCAAGTGGCTGGGACTGCATGCATGTACCACCATGCCCGGCTAATGTTT A G FAF2 Ensembl:ENSG00000113194 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs922596418 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110296,RMVar_hsa_circ_236370 8641 RMVar_ID_8641 Human_SNP_ID_262740404 A-to-I Human chr5 + 176489586 176489586 176489586 CAGAGTCTTGCTCTGTCGCTGTCACCCAGGCTAGAGTGCAGTGCCACCATCTCGACTCACTGCAA CAGAGTCTTGCTCTGTCGCTGTCACCCAGGCTCGAGTGCAGTGCCACCATCTCGACTCACTGCAA A C FAF2 Ensembl:ENSG00000113194 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1003638108 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18999,RMVar_hsa_circ_110296,RMVar_hsa_circ_236370,RMVar_hsa_circ_99413,RMVar_hsa_circ_282074,RMVar_hsa_circ_236371,RMVar_hsa_circ_326192,RMVar_hsa_circ_288618,RMVar_hsa_circ_62346,RMVar_hsa_circ_96377,RMVar_hsa_circ_236374,RMVar_hsa_circ_236375,RMVar_hsa_circ_236373,RMVar_hsa_circ_236376,RMVar_hsa_circ_311484,RMVar_hsa_circ_339854,RMVar_hsa_circ_340638,RMVar_hsa_circ_236377 8642 RMVar_ID_8642 Human_SNP_ID_262740543 A-to-I Human chr5 + 176490100 176490100 176490100 TTGGGAGGCTGAGGTGGGCGGATCACAACGTCAGGAGATCAAGACCATCCTGGCTAATACGGTGA TTGGGAGGCTGAGGTGGGCGGATCACAACGTCGGGAGATCAAGACCATCCTGGCTAATACGGTGA A G FAF2 Ensembl:ENSG00000113194 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1041541275 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18999,RMVar_hsa_circ_110296,RMVar_hsa_circ_236370,RMVar_hsa_circ_99413,RMVar_hsa_circ_282074,RMVar_hsa_circ_236371,RMVar_hsa_circ_326192,RMVar_hsa_circ_288618,RMVar_hsa_circ_62346,RMVar_hsa_circ_96377,RMVar_hsa_circ_236374,RMVar_hsa_circ_236375,RMVar_hsa_circ_236373,RMVar_hsa_circ_236376,RMVar_hsa_circ_311484,RMVar_hsa_circ_339854,RMVar_hsa_circ_340638,RMVar_hsa_circ_236377 8643 RMVar_ID_8643 Human_SNP_ID_262749990 A-to-I Human chr5 - 176525675 176525675 176525675 TAGAGACGGGGTCTCATGTTGTTTCCCAGGCTAGTCTTGAACTCCTGAACTTAAGTGATCTGCCT TAGAGACGGGGTCTCATGTTGTTTCCCAGGCTGGTCTTGAACTCCTGAACTTAAGTGATCTGCCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1390821625 Functional Loss SNV dbSNP153 33..33 33 - - - 8644 RMVar_ID_8644 Human_SNP_ID_262788867 A-to-I Human chr5 - 176657155 176657155 176657155 TGCCTGCATGTGTGTGTACACACGCATATGGGACAAGAGGCCCAGGCGGAGGCACAGCAACTTCC TGCCTGCATGTGTGTGTACACACGCATATGGGGCAAGAGGCCCAGGCGGAGGCACAGCAACTTCC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs548977433 Functional Loss SNV dbSNP153 33..33 33 - - - 8645 RMVar_ID_8645 Human_SNP_ID_262856239 A-to-I Human chr5 - 176909487 176909487 176909487 CAGGCAAATCTAGTTTCTGACAATTATTACCTATAAGACCATAGTTAGACTAGTTCCTTCCTAAT CAGGCAAATCTAGTTTCTGACAATTATTACCTGTAAGACCATAGTTAGACTAGTTCCTTCCTAAT T C UIMC1 Ensembl:ENSG00000087206 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1201734823 Functional Loss SNV dbSNP153 33..33 33 - - - 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_236399 8646 RMVar_ID_8646 Human_SNP_ID_262856458 A-to-I Human chr5 - 176910465 176910465 176910465 CATTAGGAAGGAACTAGTCTAACTATGGTCTTATAGGTAATAATTGTCAGAAACTAGATTTGCCT CATTAGGAAGGAACTAGTCTAACTATGGTCTTGTAGGTAATAATTGTCAGAAACTAGATTTGCCT T C UIMC1 Ensembl:ENSG00000087206 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1194572585 Functional Loss SNV dbSNP153 33..33 33 - - - 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_236399 8647 RMVar_ID_8647 Human_SNP_ID_262857102 A-to-I Human chr5 - 176912558 176912558 176912558 TGAGGCAGGAGAATCACTTGAACTCGGGAGGCAGAGGTTGCAGTGAGCTGAGATTGCTCCATTGC TGAGGCAGGAGAATCACTTGAACTCGGGAGGCGGAGGTTGCAGTGAGCTGAGATTGCTCCATTGC T C UIMC1 Ensembl:ENSG00000087206 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1554105815 Functional Loss SNV dbSNP153 33..33 33 - - - 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_236399 8648 RMVar_ID_8648 Human_SNP_ID_262857410 A-to-I Human chr5 - 176913823 176913823 176913823 ACAGGCAAGCACCACCATGCTGGCTAACTTTTATATTTTTTGTAGAGACGGGGGTTTCACCCTGT ACAGGCAAGCACCACCATGCTGGCTAACTTTTGTATTTTTTGTAGAGACGGGGGTTTCACCCTGT T C UIMC1 Ensembl:ENSG00000087206 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1373271573 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15392049,Human_RBP_ID_25881522 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_236399 8649 RMVar_ID_8649 Human_SNP_ID_262864787 A-to-I Human chr5 - 176942940 176942940 176942940 CTCACGCCTTAGCCTCCCAAGTAGCTGGGACTACAGGCTTGCGCCACCATGCCTGGCTAATTTTT CTCACGCCTTAGCCTCCCAAGTAGCTGGGACTGCAGGCTTGCGCCACCATGCCTGGCTAATTTTT T C UIMC1 Ensembl:ENSG00000087206 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1453869137 Functional Loss SNV dbSNP153 33..33 33 - - - 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 8650 RMVar_ID_8650 Human_SNP_ID_262864939 A-to-I Human chr5 - 176943434 176943434 176943434 AGAAGGAAGTAGCTATTTCTACCTTCTCATCCAGTAACCAGGTATCCTGCCCGCTATGTGACCAA AGAAGGAAGTAGCTATTTCTACCTTCTCATCCGGTAACCAGGTATCCTGCCCGCTATGTGACCAA T C UIMC1 Ensembl:ENSG00000087206 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs894108835 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1040762,Human_RBP_ID_5509331,Human_RBP_ID_9261953,Human_RBP_ID_9305493,Human_RBP_ID_9398696,Human_RBP_ID_17707717,Human_RBP_ID_18045247,Human_RBP_ID_18356930,Human_RBP_ID_21944489 Human_Splice_Rec_723842,Human_Splice_Rec_723843,Human_Splice_Rec_723868,Human_Splice_Rec_723869,Human_Splice_Rec_723892,Human_Splice_Rec_723893,Human_Splice_Rec_723920,Human_Splice_Rec_723921,Human_Splice_Rec_723938,Human_Splice_Rec_723939,Human_Splice_Rec_723960,Human_Splice_Rec_723961 RMVar_hsa_circ_85433,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_270515,RMVar_hsa_circ_236401,RMVar_hsa_circ_236402,RMVar_hsa_circ_279760,RMVar_hsa_circ_345315,RMVar_hsa_circ_349326,RMVar_hsa_circ_342521,RMVar_hsa_circ_271114,RMVar_hsa_circ_113131,RMVar_hsa_circ_121096,RMVar_hsa_circ_87073,RMVar_hsa_circ_236405,RMVar_hsa_circ_236409,RMVar_hsa_circ_236411,RMVar_hsa_circ_236413,RMVar_hsa_circ_75709,RMVar_hsa_circ_236412,RMVar_hsa_circ_236410,RMVar_hsa_circ_236407,RMVar_hsa_circ_236408,RMVar_hsa_circ_236406,RMVar_hsa_circ_236403,RMVar_hsa_circ_236404 8651 RMVar_ID_8651 Human_SNP_ID_262866543 A-to-I Human chr5 - 176950008 176950008 176950008 TCTTGTCTGCCAGGCTGGAGTGCAGTGGTGCGATCTCGGCTCACTGCAATCTCCACCTCCCGGAG TCTTGTCTGCCAGGCTGGAGTGCAGTGGTGCGGTCTCGGCTCACTGCAATCTCCACCTCCCGGAG T C UIMC1 Ensembl:ENSG00000087206 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1453974268 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85433,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_236399,RMVar_hsa_circ_336966,RMVar_hsa_circ_270515,RMVar_hsa_circ_236402,RMVar_hsa_circ_279760,RMVar_hsa_circ_345315,RMVar_hsa_circ_349326,RMVar_hsa_circ_342521,RMVar_hsa_circ_271114,RMVar_hsa_circ_113131,RMVar_hsa_circ_121096,RMVar_hsa_circ_236405,RMVar_hsa_circ_236409,RMVar_hsa_circ_236411,RMVar_hsa_circ_75709,RMVar_hsa_circ_236412,RMVar_hsa_circ_236410,RMVar_hsa_circ_236407,RMVar_hsa_circ_236408,RMVar_hsa_circ_236406,RMVar_hsa_circ_236403,RMVar_hsa_circ_236404 8652 RMVar_ID_8652 Human_SNP_ID_262868886 A-to-I Human chr5 - 176959608 176959608 176959608 GGGTTCACGCCATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCGCCTGCCACTACG GGGTTCACGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCTGCCACTACG T C UIMC1 Ensembl:ENSG00000087206 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1018657495 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101806,RMVar_hsa_circ_236398,RMVar_hsa_circ_345315,RMVar_hsa_circ_349326,RMVar_hsa_circ_342521,RMVar_hsa_circ_271114,RMVar_hsa_circ_113131,RMVar_hsa_circ_121096,RMVar_hsa_circ_70873,RMVar_hsa_circ_236405,RMVar_hsa_circ_236409,RMVar_hsa_circ_75709,RMVar_hsa_circ_236407,RMVar_hsa_circ_236408,RMVar_hsa_circ_236406,RMVar_hsa_circ_236403,RMVar_hsa_circ_236404,RMVar_hsa_circ_269496,RMVar_hsa_circ_328319,RMVar_hsa_circ_8543,RMVar_hsa_circ_66272,RMVar_hsa_circ_311842 8653 RMVar_ID_8653 Human_SNP_ID_262871366 A-to-I Human chr5 - 176968972 176968972 176968972 GGGGACACATCTAGGCACTGTCTACCTACCCTAGCAGATGCCAAAGGTCTCCAGGACACTGGGGG GGGGACACATCTAGGCACTGTCTACCTACCCTGGCAGATGCCAAAGGTCTCCAGGACACTGGGGG T C UIMC1 Ensembl:ENSG00000087206 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs756948887 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2919439,Human_RBP_ID_8611095 Human_miRNA_ID_1091452,Human_miRNA_ID_3079481,Human_miRNA_ID_3079482,Human_miRNA_ID_3079483 RMVar_hsa_circ_101806,RMVar_hsa_circ_236398,RMVar_hsa_circ_345315,RMVar_hsa_circ_349326,RMVar_hsa_circ_342521,RMVar_hsa_circ_271114,RMVar_hsa_circ_113131,RMVar_hsa_circ_121096,RMVar_hsa_circ_70873,RMVar_hsa_circ_236405,RMVar_hsa_circ_236409,RMVar_hsa_circ_75709,RMVar_hsa_circ_236407,RMVar_hsa_circ_236408,RMVar_hsa_circ_236406,RMVar_hsa_circ_236403,RMVar_hsa_circ_236404,RMVar_hsa_circ_269496,RMVar_hsa_circ_328319,RMVar_hsa_circ_8543,RMVar_hsa_circ_66272,RMVar_hsa_circ_311842,RMVar_hsa_circ_14724,RMVar_hsa_circ_328813,RMVar_hsa_circ_366032 8654 RMVar_ID_8654 Human_SNP_ID_262872699 A-to-I Human chr5 - 176973820 176973820 176973820 TGGCTCACTACAACCTCTGCCTCCTGGGCTCAAGTGATCCTCTCATCTCAGCCTCCCAAGTAGCT TGGCTCACTACAACCTCTGCCTCCTGGGCTCAGGTGATCCTCTCATCTCAGCCTCCCAAGTAGCT T C UIMC1 Ensembl:ENSG00000087206 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs553400173 Functional Loss SNV dbSNP153 33..33 33 - - - 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_64640 8655 RMVar_ID_8655 Human_SNP_ID_262878395 A-to-I Human chr5 - 176993350 176993350 176993350 ACCTTGTCTCTACAAAAAATAAAAAGTAAATTAGCTGGGTGTGGTGGCACATGCCTGTGGTCCTA ACCTTGTCTCTACAAAAAATAAAAAGTAAATTGGCTGGGTGTGGTGGCACATGCCTGTGGTCCTA T C UIMC1 Ensembl:ENSG00000087206 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs374343212 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113131,RMVar_hsa_circ_75709,RMVar_hsa_circ_236403,RMVar_hsa_circ_236404 8656 RMVar_ID_8656 Human_SNP_ID_262878396 A-to-I Human chr5 - 176993350 176993350 176993350 ACCTTGTCTCTACAAAAAATAAAAAGTAAATTAGCTGGGTGTGGTGGCACATGCCTGTGGTCCTA ACCTTGTCTCTACAAAAAATAAAAAGTAAATTCGCTGGGTGTGGTGGCACATGCCTGTGGTCCTA T G UIMC1 Ensembl:ENSG00000087206 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs374343212 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113131,RMVar_hsa_circ_75709,RMVar_hsa_circ_236403,RMVar_hsa_circ_236404 8657 RMVar_ID_8657 Human_SNP_ID_262890639 A-to-I Human chr5 + 177039925 177039925 177039925 TGCCTTGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGAAGGCCAAGGTGGGTGG TGCCTTGGCCGGGCGCGGTGGCTCACGCCTGTCATCCCAGCACTTTGGAAGGCCAAGGTGGGTGG A C ZNF346 Ensembl:ENSG00000113761 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1257469925 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80510,RMVar_hsa_circ_236418 8658 RMVar_ID_8658 Human_SNP_ID_262891339 A-to-I Human chr5 + 177043026 177043026 177043026 GGCACGCGCCACCACACCCAGCTAATTTTTGTATTTTTAGTAGAGATAGGGTTTCACCAGGTTGG GGCACGCGCCACCACACCCAGCTAATTTTTGTTTTTTTAGTAGAGATAGGGTTTCACCAGGTTGG A T ZNF346 Ensembl:ENSG00000113761 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1319461109 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19708,RMVar_hsa_circ_80510,RMVar_hsa_circ_307082,RMVar_hsa_circ_236418,RMVar_hsa_circ_294862,RMVar_hsa_circ_273241,RMVar_hsa_circ_236421,RMVar_hsa_circ_236422,RMVar_hsa_circ_236420,RMVar_hsa_circ_236423,RMVar_hsa_circ_370957 8659 RMVar_ID_8659 Human_SNP_ID_262891340 A-to-I Human chr5 + 177043032 177043032 177043032 CGCCACCACACCCAGCTAATTTTTGTATTTTTAGTAGAGATAGGGTTTCACCAGGTTGGCCAGGC CGCCACCACACCCAGCTAATTTTTGTATTTTTGGTAGAGATAGGGTTTCACCAGGTTGGCCAGGC A G ZNF346 Ensembl:ENSG00000113761 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1299170726 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25882071 RMVar_hsa_circ_19708,RMVar_hsa_circ_80510,RMVar_hsa_circ_307082,RMVar_hsa_circ_236418,RMVar_hsa_circ_294862,RMVar_hsa_circ_273241,RMVar_hsa_circ_236421,RMVar_hsa_circ_236422,RMVar_hsa_circ_236420,RMVar_hsa_circ_236423,RMVar_hsa_circ_370957 8660 RMVar_ID_8660 Human_SNP_ID_262891449 A-to-I Human chr5 + 177043516 177043516 177043516 GGCTGGGTGCGGTGGCTCATACCTGTAATCCTAGCAATTTAGGTGGCTGAGGCAGGCGGATTGCT GGCTGGGTGCGGTGGCTCATACCTGTAATCCTGGCAATTTAGGTGGCTGAGGCAGGCGGATTGCT A G ZNF346 Ensembl:ENSG00000113761 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs971547384 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19708,RMVar_hsa_circ_80510,RMVar_hsa_circ_307082,RMVar_hsa_circ_236418,RMVar_hsa_circ_294862,RMVar_hsa_circ_273241,RMVar_hsa_circ_236421,RMVar_hsa_circ_236422,RMVar_hsa_circ_236420,RMVar_hsa_circ_236423,RMVar_hsa_circ_370957 8661 RMVar_ID_8661 Human_SNP_ID_262891885 A-to-I Human chr5 + 177045448 177045448 177045448 ATGATCTCGGCTCACTGCAAGCTCTACCTCCCAGGTTCATGCCATTCTTCAGCCTCAGCCTCCCA ATGATCTCGGCTCACTGCAAGCTCTACCTCCCGGGTTCATGCCATTCTTCAGCCTCAGCCTCCCA A G ZNF346 Ensembl:ENSG00000113761 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs564198830 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25882119 RMVar_hsa_circ_19708,RMVar_hsa_circ_80510,RMVar_hsa_circ_307082,RMVar_hsa_circ_236418,RMVar_hsa_circ_273241,RMVar_hsa_circ_236421,RMVar_hsa_circ_236422,RMVar_hsa_circ_59370,RMVar_hsa_circ_285547 8662 RMVar_ID_8662 Human_SNP_ID_262891889 A-to-I Human chr5 + 177045480 177045480 177045480 AGGTTCATGCCATTCTTCAGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGTGCCCACCACCATG AGGTTCATGCCATTCTTCAGCCTCAGCCTCCCTAGTAGCTGGGACTACAGGTGCCCACCACCATG A T ZNF346 Ensembl:ENSG00000113761 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1021500554 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19708,RMVar_hsa_circ_80510,RMVar_hsa_circ_307082,RMVar_hsa_circ_236418,RMVar_hsa_circ_273241,RMVar_hsa_circ_236421,RMVar_hsa_circ_236422,RMVar_hsa_circ_59370,RMVar_hsa_circ_285547 8663 RMVar_ID_8663 Human_SNP_ID_262892051 A-to-I Human chr5 + 177046207 177046207 177046207 CCTGTAGTCCCAGCTTCTTGGGAGACTGAGGCAAGAGAATCGCTTGAACCCGGGAGCTGGAGGTT CCTGTAGTCCCAGCTTCTTGGGAGACTGAGGCCAGAGAATCGCTTGAACCCGGGAGCTGGAGGTT A C ZNF346 Ensembl:ENSG00000113761 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1336191745 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19708,RMVar_hsa_circ_80510,RMVar_hsa_circ_307082,RMVar_hsa_circ_236418,RMVar_hsa_circ_273241,RMVar_hsa_circ_236421,RMVar_hsa_circ_236422,RMVar_hsa_circ_59370,RMVar_hsa_circ_285547 8664 RMVar_ID_8664 Human_SNP_ID_262892056 A-to-I Human chr5 + 177046221 177046221 177046221 TTCTTGGGAGACTGAGGCAAGAGAATCGCTTGAACCCGGGAGCTGGAGGTTGCAGTGAGCTGAGA TTCTTGGGAGACTGAGGCAAGAGAATCGCTTGCACCCGGGAGCTGGAGGTTGCAGTGAGCTGAGA A C ZNF346 Ensembl:ENSG00000113761 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs994027565 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19708,RMVar_hsa_circ_80510,RMVar_hsa_circ_307082,RMVar_hsa_circ_236418,RMVar_hsa_circ_273241,RMVar_hsa_circ_236421,RMVar_hsa_circ_236422,RMVar_hsa_circ_59370,RMVar_hsa_circ_285547 8665 RMVar_ID_8665 Human_SNP_ID_262892074 A-to-I Human chr5 + 177046271 177046271 177046271 TGCAGTGAGCTGAGATCGCACCATTGTACACCAGCCTGGGGGACAGAGCAAGACCTCGTCTCAAA TGCAGTGAGCTGAGATCGCACCATTGTACACCGGCCTGGGGGACAGAGCAAGACCTCGTCTCAAA A G ZNF346 Ensembl:ENSG00000113761 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1337314538 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25939745 RMVar_hsa_circ_19708,RMVar_hsa_circ_80510,RMVar_hsa_circ_307082,RMVar_hsa_circ_236418,RMVar_hsa_circ_273241,RMVar_hsa_circ_236421,RMVar_hsa_circ_236422,RMVar_hsa_circ_59370,RMVar_hsa_circ_285547 8666 RMVar_ID_8666 Human_SNP_ID_262892680 A-to-I Human chr5 + 177048570 177048570 177048570 TTGAACCCCAGAGGCAGAGGTTGCAGTGAGTCAAGATCGTGCCATTGCACTCCAGCCTGGGCAAC TTGAACCCCAGAGGCAGAGGTTGCAGTGAGTCGAGATCGTGCCATTGCACTCCAGCCTGGGCAAC A G ZNF346 Ensembl:ENSG00000113761 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs970771784 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19708,RMVar_hsa_circ_80510,RMVar_hsa_circ_307082,RMVar_hsa_circ_236418,RMVar_hsa_circ_273241,RMVar_hsa_circ_236421,RMVar_hsa_circ_236422,RMVar_hsa_circ_59370,RMVar_hsa_circ_285547 8667 RMVar_ID_8667 Human_SNP_ID_262892800 A-to-I Human chr5 + 177048930 177048930 177048930 CCTCAGCCTCCTGAGTAGCTGGGATTACAGGCATGCACTACCACACCCAGCTAATTTTGTATTTT CCTCAGCCTCCTGAGTAGCTGGGATTACAGGCGTGCACTACCACACCCAGCTAATTTTGTATTTT A G ZNF346 Ensembl:ENSG00000113761 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs866133325 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19708,RMVar_hsa_circ_80510,RMVar_hsa_circ_307082,RMVar_hsa_circ_236418,RMVar_hsa_circ_273241,RMVar_hsa_circ_236421,RMVar_hsa_circ_236422,RMVar_hsa_circ_59370,RMVar_hsa_circ_285547 8668 RMVar_ID_8668 Human_SNP_ID_262892805 A-to-I Human chr5 + 177048966 177048961 177048967 ACTACCACACCCAGCTAATTTTGTATTTTTTTAGTAGAGACTGAGTTTCACCATGTTGGCCAGGC ACTACCACACCCAGCTAATTTTGTATTT______TAGAGACTGAGTTTCACCATGTTGGCCAGGC TTTTTAG T ZNF346 Ensembl:ENSG00000113761 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1188206117 Functional Loss DEL dbSNP153 29..34 33 - - - Human_RBP_ID_7420527,Human_RBP_ID_15395277 RMVar_hsa_circ_19708,RMVar_hsa_circ_80510,RMVar_hsa_circ_307082,RMVar_hsa_circ_236418,RMVar_hsa_circ_273241,RMVar_hsa_circ_236421,RMVar_hsa_circ_236422,RMVar_hsa_circ_59370,RMVar_hsa_circ_285547 8669 RMVar_ID_8669 Human_SNP_ID_262892806 A-to-I Human chr5 + 177048966 177048966 177048966 ACTACCACACCCAGCTAATTTTGTATTTTTTTAGTAGAGACTGAGTTTCACCATGTTGGCCAGGC ACTACCACACCCAGCTAATTTTGTATTTTTTTGGTAGAGACTGAGTTTCACCATGTTGGCCAGGC A G ZNF346 Ensembl:ENSG00000113761 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs763448567 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7420527,Human_RBP_ID_15395277 RMVar_hsa_circ_19708,RMVar_hsa_circ_80510,RMVar_hsa_circ_307082,RMVar_hsa_circ_236418,RMVar_hsa_circ_273241,RMVar_hsa_circ_236421,RMVar_hsa_circ_236422,RMVar_hsa_circ_59370,RMVar_hsa_circ_285547 8670 RMVar_ID_8670 Human_SNP_ID_262892808 A-to-I Human chr5 + 177048969 177048969 177048969 ACCACACCCAGCTAATTTTGTATTTTTTTAGTAGAGACTGAGTTTCACCATGTTGGCCAGGCTGG ACCACACCCAGCTAATTTTGTATTTTTTTAGTGGAGACTGAGTTTCACCATGTTGGCCAGGCTGG A G ZNF346 Ensembl:ENSG00000113761 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs544720363 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7420527,Human_RBP_ID_15395277 RMVar_hsa_circ_19708,RMVar_hsa_circ_80510,RMVar_hsa_circ_307082,RMVar_hsa_circ_236418,RMVar_hsa_circ_273241,RMVar_hsa_circ_236421,RMVar_hsa_circ_236422,RMVar_hsa_circ_59370,RMVar_hsa_circ_285547 8671 RMVar_ID_8671 Human_SNP_ID_262892813 A-to-I Human chr5 + 177048986 177048985 177048986 TTGTATTTTTTTAGTAGAGACTGAGTTTCACCATGTTGGCCAGGCTGGTCTCAGAACTCCTGAGT TTGTATTTTTTTAGTAGAGACTGAGTTTCACC_TGTTGGCCAGGCTGGTCTCAGAACTCCTGAGT CA C ZNF346 Ensembl:ENSG00000113761 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1295405695 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_7420527,Human_RBP_ID_15395277 RMVar_hsa_circ_19708,RMVar_hsa_circ_80510,RMVar_hsa_circ_307082,RMVar_hsa_circ_236418,RMVar_hsa_circ_273241,RMVar_hsa_circ_236421,RMVar_hsa_circ_236422,RMVar_hsa_circ_59370,RMVar_hsa_circ_285547 8672 RMVar_ID_8672 Human_SNP_ID_262892814 A-to-I Human chr5 + 177048986 177048986 177048986 TTGTATTTTTTTAGTAGAGACTGAGTTTCACCATGTTGGCCAGGCTGGTCTCAGAACTCCTGAGT TTGTATTTTTTTAGTAGAGACTGAGTTTCACCGTGTTGGCCAGGCTGGTCTCAGAACTCCTGAGT A G ZNF346 Ensembl:ENSG00000113761 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs958977165 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7420527,Human_RBP_ID_15395277 RMVar_hsa_circ_19708,RMVar_hsa_circ_80510,RMVar_hsa_circ_307082,RMVar_hsa_circ_236418,RMVar_hsa_circ_273241,RMVar_hsa_circ_236421,RMVar_hsa_circ_236422,RMVar_hsa_circ_59370,RMVar_hsa_circ_285547 8673 RMVar_ID_8673 Human_SNP_ID_262893477 A-to-I Human chr5 + 177051443 177051443 177051443 GTGATCCGCCCACCTCGGCCTCCCAAAGTGCTAGAATTACAGGCGTGAGCCACCGCGCCCAGCCC GTGATCCGCCCACCTCGGCCTCCCAAAGTGCTGGAATTACAGGCGTGAGCCACCGCGCCCAGCCC A G ZNF346 Ensembl:ENSG00000113761 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1322127078 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 8674 RMVar_ID_8674 Human_SNP_ID_262893559 A-to-I Human chr5 + 177051719 177051719 177051719 CACCACCACGCCCGGCTAATTTTTGTATTTTTAGTAGAGACAAGGTTTCACCATGTTGGGCAGGA CACCACCACGCCCGGCTAATTTTTGTATTTTTGGTAGAGACAAGGTTTCACCATGTTGGGCAGGA A G ZNF346-IT1,ZNF346 Ensembl:ENSG00000251666,Ensembl:ENSG00000113761 lincRNA,Protein coding exon,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs765426249 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 8675 RMVar_ID_8675 Human_SNP_ID_262893615 A-to-I Human chr5 + 177051893 177051893 177051893 AAATTAAAAAATTTTTAAGCCCAGCCAGGCATAGTGGCTTATGCTGTAATCCAAACACTTTGGGA AAATTAAAAAATTTTTAAGCCCAGCCAGGCATCGTGGCTTATGCTGTAATCCAAACACTTTGGGA A C ZNF346-IT1,ZNF346 Ensembl:ENSG00000251666,Ensembl:ENSG00000113761 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1463625937 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5250702 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 8676 RMVar_ID_8676 Human_SNP_ID_262893629 A-to-I Human chr5 + 177051954 177051954 177051954 GGGATGCCAAGGTAGGAGGATCACTTGAGCCTAAGAGTTCAAGACCAGCCTGGCCAACATGGTGA GGGATGCCAAGGTAGGAGGATCACTTGAGCCTCAGAGTTCAAGACCAGCCTGGCCAACATGGTGA A C ZNF346-IT1,ZNF346 Ensembl:ENSG00000251666,Ensembl:ENSG00000113761 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs144414758 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5250702 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 8677 RMVar_ID_8677 Human_SNP_ID_262893630 A-to-I Human chr5 + 177051954 177051954 177051954 GGGATGCCAAGGTAGGAGGATCACTTGAGCCTAAGAGTTCAAGACCAGCCTGGCCAACATGGTGA GGGATGCCAAGGTAGGAGGATCACTTGAGCCTGAGAGTTCAAGACCAGCCTGGCCAACATGGTGA A G ZNF346-IT1,ZNF346 Ensembl:ENSG00000251666,Ensembl:ENSG00000113761 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs144414758 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5250702 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 8678 RMVar_ID_8678 Human_SNP_ID_262893660 A-to-I Human chr5 + 177052141 177052138 177052142 GAGATATGATTGTGCCACTGTATTCCAACCTGAGTGAGAGCGAGAACATGTATCAAAAAAACAAT GAGATATGATTGTGCCACTGTATTCCAACC____TGAGAGCGAGAACATGTATCAAAAAAACAAT CTGAG C ZNF346-IT1,ZNF346 Ensembl:ENSG00000251666,Ensembl:ENSG00000113761 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1222188830 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_5250789,Human_RBP_ID_15395409 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 8679 RMVar_ID_8679 Human_SNP_ID_262893691 A-to-I Human chr5 + 177052223 177052223 177052223 ACAGTCTCACTCTGTCTCCCAGGCTGGAGTACAATGACACCATCTCACCTCACTGCAACGTCTGC ACAGTCTCACTCTGTCTCCCAGGCTGGAGTACGATGACACCATCTCACCTCACTGCAACGTCTGC A G ZNF346-IT1,ZNF346 Ensembl:ENSG00000251666,Ensembl:ENSG00000113761 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1325671683 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7420534,Human_RBP_ID_15395415,Human_RBP_ID_17529257 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 8680 RMVar_ID_8680 Human_SNP_ID_262893881 A-to-I Human chr5 + 177053106 177053106 177053106 TTGGGAGGCCAAGGCAGGTGGATCATAAGGTCAAGAGGGCGAGACCATCCTGGCCAATATGGTGA TTGGGAGGCCAAGGCAGGTGGATCATAAGGTCGAGAGGGCGAGACCATCCTGGCCAATATGGTGA A G ZNF346 Ensembl:ENSG00000113761 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1034055541 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 8681 RMVar_ID_8681 Human_SNP_ID_262893909 A-to-I Human chr5 + 177053193 177053193 177053193 GAAAAATTAGCTGGACGTGGTGACACACGCCTATAGTCCCAGCTACTTAGGAGGCTGAGGCAGGA GAAAAATTAGCTGGACGTGGTGACACACGCCTGTAGTCCCAGCTACTTAGGAGGCTGAGGCAGGA A G ZNF346 Ensembl:ENSG00000113761 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1399569095 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 8682 RMVar_ID_8682 Human_SNP_ID_262894228 A-to-I Human chr5 + 177054345 177054345 177054345 CACCCACCTTGGCCTCCCAAAGTGCTGGGATTACAGACATGAGCCACCATGCCCAATCTGGCTAT CACCCACCTTGGCCTCCCAAAGTGCTGGGATTGCAGACATGAGCCACCATGCCCAATCTGGCTAT A G ZNF346 Ensembl:ENSG00000113761 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs890944803 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 8683 RMVar_ID_8683 Human_SNP_ID_262894229 A-to-I Human chr5 + 177054345 177054345 177054345 CACCCACCTTGGCCTCCCAAAGTGCTGGGATTACAGACATGAGCCACCATGCCCAATCTGGCTAT CACCCACCTTGGCCTCCCAAAGTGCTGGGATTTCAGACATGAGCCACCATGCCCAATCTGGCTAT A T ZNF346 Ensembl:ENSG00000113761 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs890944803 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 8684 RMVar_ID_8684 Human_SNP_ID_262894288 A-to-I Human chr5 + 177054538 177054538 177054538 CTCCTGCCTCAGCCTCCCGTGTAGCTGGGATTACAGGTGCCCACCACCATGCCCGGCTAATTTTT CTCCTGCCTCAGCCTCCCGTGTAGCTGGGATTGCAGGTGCCCACCACCATGCCCGGCTAATTTTT A G ZNF346 Ensembl:ENSG00000113761 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1171656669 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 8685 RMVar_ID_8685 Human_SNP_ID_262894452 A-to-I Human chr5 + 177055199 177055199 177055199 GGGATTATAGACACCCACCACCAAACTCGGCTAATTTTTGTGTTTTTAGTAGAGACGGAGTTTCA GGGATTATAGACACCCACCACCAAACTCGGCTGATTTTTGTGTTTTTAGTAGAGACGGAGTTTCA A G ZNF346 Ensembl:ENSG00000113761 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs573300386 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 8686 RMVar_ID_8686 Human_SNP_ID_262894469 A-to-I Human chr5 + 177055268 177055268 177055268 GTTGGCCAGGCTGGTCTCAAACTACTGACCTCAGGTGATCCACCTACCTCGGCCTCCCAAAGTGC GTTGGCCAGGCTGGTCTCAAACTACTGACCTCCGGTGATCCACCTACCTCGGCCTCCCAAAGTGC A C ZNF346 Ensembl:ENSG00000113761 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1234738348 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 8687 RMVar_ID_8687 Human_SNP_ID_262894587 A-to-I Human chr5 + 177055770 177055770 177055770 CGAGACCAGCCTGGCCAAGATGGCAAAACCCCATCTCTACTAAAAATACAAAAATTGGCCGGGTG CGAGACCAGCCTGGCCAAGATGGCAAAACCCCGTCTCTACTAAAAATACAAAAATTGGCCGGGTG A G ZNF346 Ensembl:ENSG00000113761 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1324292113 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 8688 RMVar_ID_8688 Human_SNP_ID_262894609 A-to-I Human chr5 + 177055892 177055892 177055892 GAGGTCAGGAGCTGGAGACCAGTCTGACCAACAAGGAGAAACCCCGTCTCTATTAAAAATACAAA GAGGTCAGGAGCTGGAGACCAGTCTGACCAACCAGGAGAAACCCCGTCTCTATTAAAAATACAAA A C ZNF346 Ensembl:ENSG00000113761 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1003463497 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 8689 RMVar_ID_8689 Human_SNP_ID_262894610 A-to-I Human chr5 + 177055892 177055892 177055892 GAGGTCAGGAGCTGGAGACCAGTCTGACCAACAAGGAGAAACCCCGTCTCTATTAAAAATACAAA GAGGTCAGGAGCTGGAGACCAGTCTGACCAACGAGGAGAAACCCCGTCTCTATTAAAAATACAAA A G ZNF346 Ensembl:ENSG00000113761 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1003463497 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 8690 RMVar_ID_8690 Human_SNP_ID_262894630 A-to-I Human chr5 + 177055965 177055965 177055965 AGGCATGGTGGCATGCACCCGTAATCCCAGCTACTCTGAAGGCTGAGGCACAAGAATCACTTGAA AGGCATGGTGGCATGCACCCGTAATCCCAGCTGCTCTGAAGGCTGAGGCACAAGAATCACTTGAA A G ZNF346 Ensembl:ENSG00000113761 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1317900755 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 8691 RMVar_ID_8691 Human_SNP_ID_262894638 A-to-I Human chr5 + 177056017 177056017 177056017 AGAATCACTTGAACCCAGGAGGAGGAGGTTGCAGTGAGCCAAGATCGTGTCACTGCACTCCAGCC AGAATCACTTGAACCCAGGAGGAGGAGGTTGCGGTGAGCCAAGATCGTGTCACTGCACTCCAGCC A G ZNF346 Ensembl:ENSG00000113761 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs966230061 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 8692 RMVar_ID_8692 Human_SNP_ID_262894641 A-to-I Human chr5 + 177056025 177056025 177056025 TTGAACCCAGGAGGAGGAGGTTGCAGTGAGCCAAGATCGTGTCACTGCACTCCAGCCTGGGCAAA TTGAACCCAGGAGGAGGAGGTTGCAGTGAGCCCAGATCGTGTCACTGCACTCCAGCCTGGGCAAA A C ZNF346 Ensembl:ENSG00000113761 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1453946986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9174921 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 8693 RMVar_ID_8693 Human_SNP_ID_262894642 A-to-I Human chr5 + 177056025 177056025 177056025 TTGAACCCAGGAGGAGGAGGTTGCAGTGAGCCAAGATCGTGTCACTGCACTCCAGCCTGGGCAAA TTGAACCCAGGAGGAGGAGGTTGCAGTGAGCCGAGATCGTGTCACTGCACTCCAGCCTGGGCAAA A G ZNF346 Ensembl:ENSG00000113761 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1453946986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9174921 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 8694 RMVar_ID_8694 Human_SNP_ID_262894704 A-to-I Human chr5 + 177056195 177056195 177056195 TGAACCTGGTTGCAGTGAGCTGAGATCACACCACTGCACTGGGCGACAGAGCAAGGCTCCATCTC TGAACCTGGTTGCAGTGAGCTGAGATCACACCGCTGCACTGGGCGACAGAGCAAGGCTCCATCTC A G ZNF346 Ensembl:ENSG00000113761 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1253315465 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7420546 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 8695 RMVar_ID_8695 Human_SNP_ID_262895047 A-to-I Human chr5 + 177057617 177057617 177057617 AAAATTAGCTGGGCATGGTGGTGTGCACCTGTAATCCCAACTACTCAGGATGCTGAGGCAGGAGA AAAATTAGCTGGGCATGGTGGTGTGCACCTGTTATCCCAACTACTCAGGATGCTGAGGCAGGAGA A T ZNF346 Ensembl:ENSG00000113761 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1027598729 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 8696 RMVar_ID_8696 Human_SNP_ID_262897834 A-to-I Human chr5 + 177069266 177069266 177069266 ATCACTTGAGGTCAGGAGTTCCAGACCAGCCTAGCCAACATGGTGAAACCCTGTCTCTACTAAAA ATCACTTGAGGTCAGGAGTTCCAGACCAGCCTGGCCAACATGGTGAAACCCTGTCTCTACTAAAA A G ZNF346 Ensembl:ENSG00000113761 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1325707406 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_236428 8697 RMVar_ID_8697 Human_SNP_ID_262897849 A-to-I Human chr5 + 177069305 177069305 177069305 ATGGTGAAACCCTGTCTCTACTAAAAATACAAAAATTAGCTGGTCGTGGTGGTGGATGCCTGTAA ATGGTGAAACCCTGTCTCTACTAAAAATACAACAATTAGCTGGTCGTGGTGGTGGATGCCTGTAA A C ZNF346 Ensembl:ENSG00000113761 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1258876037 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_236428 8698 RMVar_ID_8698 Human_SNP_ID_262897861 A-to-I Human chr5 + 177069358 177069358 177069358 GGATGCCTGTAATCTCAGCTGCTCGCTGAGGCAGGAGAATCGCTTGAACCTGGGAGGCGGAGGTT GGATGCCTGTAATCTCAGCTGCTCGCTGAGGCGGGAGAATCGCTTGAACCTGGGAGGCGGAGGTT A G ZNF346 Ensembl:ENSG00000113761 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs946461970 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_236428 8699 RMVar_ID_8699 Human_SNP_ID_262898374 A-to-I Human chr5 + 177071507 177071506 177071507 AGGAGATCGAGACCATCCTGGCTAACACGGTGAAACCCCATCTCTACTAAAAATACAAAAAATTA AGGAGATCGAGACCATCCTGGCTAACACGGTG_AACCCCATCTCTACTAAAAATACAAAAAATTA GA G ZNF346 Ensembl:ENSG00000113761 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs746177489 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_236428 8700 RMVar_ID_8700 Human_SNP_ID_262898814 A-to-I Human chr5 + 177073354 177073354 177073354 GAAACAGCGTCTCACTCTGTCACACAGGCTGGAATGCAGTGGTGCAAACACAGCTCATTGCAGCC GAAACAGCGTCTCACTCTGTCACACAGGCTGGCATGCAGTGGTGCAAACACAGCTCATTGCAGCC A C ZNF346 Ensembl:ENSG00000113761 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1208451419 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_236428 8701 RMVar_ID_8701 Human_SNP_ID_262899456 A-to-I Human chr5 + 177076043 177076043 177076043 CACTCCGTTGCCCAGGCTGGTCTCAAACTCCTAGGCTCAAGGAATCCTCCTCGCTCAGCCTCCTG CACTCCGTTGCCCAGGCTGGTCTCAAACTCCTGGGCTCAAGGAATCCTCCTCGCTCAGCCTCCTG A G ZNF346 Ensembl:ENSG00000113761 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs939627905 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_236428 8702 RMVar_ID_8702 Human_SNP_ID_262917709 A-to-I Human chr5 + 177137888 177137888 177137888 GACAGATCACCTGAGGTCAGGAGTTTGAGACCAGTCTGGCCAACATGGTGAAACTCCGTCTCTAC GACAGATCACCTGAGGTCAGGAGTTTGAGACCGGTCTGGCCAACATGGTGAAACTCCGTCTCTAC A G NSD1 Ensembl:ENSG00000165671 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs958957872 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15396252 RMVar_hsa_circ_6376,RMVar_hsa_circ_109213,RMVar_hsa_circ_296651,RMVar_hsa_circ_322685,RMVar_hsa_circ_374749,RMVar_hsa_circ_236431,RMVar_hsa_circ_99866,RMVar_hsa_circ_236434,RMVar_hsa_circ_236435,RMVar_hsa_circ_236436,RMVar_hsa_circ_54322,RMVar_hsa_circ_325752,RMVar_hsa_circ_331791,RMVar_hsa_circ_97595,RMVar_hsa_circ_236437,RMVar_hsa_circ_236438 8703 RMVar_ID_8703 Human_SNP_ID_262918068 A-to-I Human chr5 + 177139166 177139166 177139166 TCAGCTATTTGGGAGGCTGAGGCAGGAGAATCACTTGAACCCGGGAGGCTGAGGTTGCAGTGAGC TCAGCTATTTGGGAGGCTGAGGCAGGAGAATCTCTTGAACCCGGGAGGCTGAGGTTGCAGTGAGC A T NSD1 Ensembl:ENSG00000165671 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1254060557 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6376,RMVar_hsa_circ_109213,RMVar_hsa_circ_296651,RMVar_hsa_circ_322685,RMVar_hsa_circ_374749,RMVar_hsa_circ_236431,RMVar_hsa_circ_99866,RMVar_hsa_circ_236434,RMVar_hsa_circ_236435,RMVar_hsa_circ_236436,RMVar_hsa_circ_54322,RMVar_hsa_circ_325752,RMVar_hsa_circ_331791,RMVar_hsa_circ_97595,RMVar_hsa_circ_236437,RMVar_hsa_circ_236438 8704 RMVar_ID_8704 Human_SNP_ID_262918117 A-to-I Human chr5 + 177139308 177139308 177139308 CGACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCTGGGCGTGGTGGCAGGCTCGG CGACATGGTGAAACCCCGTCTCTACTAAAAATGCAAAAATTAGCTGGGCGTGGTGGCAGGCTCGG A G NSD1 Ensembl:ENSG00000165671 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs930246611 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15396266,Human_RBP_ID_25882402 RMVar_hsa_circ_6376,RMVar_hsa_circ_109213,RMVar_hsa_circ_296651,RMVar_hsa_circ_322685,RMVar_hsa_circ_374749,RMVar_hsa_circ_236431,RMVar_hsa_circ_99866,RMVar_hsa_circ_236434,RMVar_hsa_circ_236435,RMVar_hsa_circ_236436,RMVar_hsa_circ_54322,RMVar_hsa_circ_325752,RMVar_hsa_circ_331791,RMVar_hsa_circ_97595,RMVar_hsa_circ_236437,RMVar_hsa_circ_236438 8705 RMVar_ID_8705 Human_SNP_ID_262918135 A-to-I Human chr5 + 177139357 177139357 177139357 GTGGTGGCAGGCTCGGGAGGTTGAGGCAGGAGAATCACTTGAACCCGGGAGGCGGAGGTTGCAGT GTGGTGGCAGGCTCGGGAGGTTGAGGCAGGAGGATCACTTGAACCCGGGAGGCGGAGGTTGCAGT A G NSD1 Ensembl:ENSG00000165671 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1394599761 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6376,RMVar_hsa_circ_109213,RMVar_hsa_circ_296651,RMVar_hsa_circ_322685,RMVar_hsa_circ_374749,RMVar_hsa_circ_236431,RMVar_hsa_circ_99866,RMVar_hsa_circ_236434,RMVar_hsa_circ_236435,RMVar_hsa_circ_236436,RMVar_hsa_circ_54322,RMVar_hsa_circ_325752,RMVar_hsa_circ_331791,RMVar_hsa_circ_97595,RMVar_hsa_circ_236437,RMVar_hsa_circ_236438 8706 RMVar_ID_8706 Human_SNP_ID_262918248 A-to-I Human chr5 + 177139746 177139746 177139746 GGAAGCCGAGACAAAAGGATTGCTTGGGGCCCAGAGTTTGAAACTAGACTGGGCAACATAGTGAG GGAAGCCGAGACAAAAGGATTGCTTGGGGCCCGGAGTTTGAAACTAGACTGGGCAACATAGTGAG A G NSD1 Ensembl:ENSG00000165671 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs973368566 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15396270 RMVar_hsa_circ_6376,RMVar_hsa_circ_109213,RMVar_hsa_circ_296651,RMVar_hsa_circ_322685,RMVar_hsa_circ_374749,RMVar_hsa_circ_236431,RMVar_hsa_circ_99866,RMVar_hsa_circ_236434,RMVar_hsa_circ_236435,RMVar_hsa_circ_236436,RMVar_hsa_circ_54322,RMVar_hsa_circ_325752,RMVar_hsa_circ_331791,RMVar_hsa_circ_97595,RMVar_hsa_circ_236437,RMVar_hsa_circ_236438 8707 RMVar_ID_8707 Human_SNP_ID_262918251 A-to-I Human chr5 + 177139768 177139768 177139768 CTTGGGGCCCAGAGTTTGAAACTAGACTGGGCAACATAGTGAGATCCTGTCTCTACACTCAGTTG CTTGGGGCCCAGAGTTTGAAACTAGACTGGGCGACATAGTGAGATCCTGTCTCTACACTCAGTTG A G NSD1 Ensembl:ENSG00000165671 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1046716074 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6376,RMVar_hsa_circ_109213,RMVar_hsa_circ_296651,RMVar_hsa_circ_322685,RMVar_hsa_circ_374749,RMVar_hsa_circ_236431,RMVar_hsa_circ_99866,RMVar_hsa_circ_236434,RMVar_hsa_circ_236435,RMVar_hsa_circ_236436,RMVar_hsa_circ_54322,RMVar_hsa_circ_325752,RMVar_hsa_circ_331791,RMVar_hsa_circ_97595,RMVar_hsa_circ_236437,RMVar_hsa_circ_236438 8708 RMVar_ID_8708 Human_SNP_ID_262918252 A-to-I Human chr5 + 177139771 177139771 177139771 GGGGCCCAGAGTTTGAAACTAGACTGGGCAACATAGTGAGATCCTGTCTCTACACTCAGTTGGTT GGGGCCCAGAGTTTGAAACTAGACTGGGCAACGTAGTGAGATCCTGTCTCTACACTCAGTTGGTT A G NSD1 Ensembl:ENSG00000165671 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1362559872 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6376,RMVar_hsa_circ_109213,RMVar_hsa_circ_296651,RMVar_hsa_circ_322685,RMVar_hsa_circ_374749,RMVar_hsa_circ_236431,RMVar_hsa_circ_99866,RMVar_hsa_circ_236434,RMVar_hsa_circ_236435,RMVar_hsa_circ_236436,RMVar_hsa_circ_54322,RMVar_hsa_circ_325752,RMVar_hsa_circ_331791,RMVar_hsa_circ_97595,RMVar_hsa_circ_236437,RMVar_hsa_circ_236438 8709 RMVar_ID_8709 Human_SNP_ID_262918276 A-to-I Human chr5 + 177139830 177139830 177139830 TTGGTTGTGGTGGTATGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGTAGTAGGATCACTT TTGGTTGTGGTGGTATGCCTGTAGTCCCAGCTGCTCAGGAGGCTGAGGCAGTAGTAGGATCACTT A G NSD1 Ensembl:ENSG00000165671 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1414894206 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6376,RMVar_hsa_circ_109213,RMVar_hsa_circ_296651,RMVar_hsa_circ_322685,RMVar_hsa_circ_374749,RMVar_hsa_circ_236431,RMVar_hsa_circ_99866,RMVar_hsa_circ_236434,RMVar_hsa_circ_236435,RMVar_hsa_circ_236436,RMVar_hsa_circ_54322,RMVar_hsa_circ_325752,RMVar_hsa_circ_331791,RMVar_hsa_circ_97595,RMVar_hsa_circ_236437,RMVar_hsa_circ_236438 8710 RMVar_ID_8710 Human_SNP_ID_262919291 A-to-I Human chr5 + 177143859 177143859 177143859 GGCTGGAGTGCAAAATGGCACGATCTTGGCTCACTGCAACCTCCACCTCATGGGTTCAAGTTGAT GGCTGGAGTGCAAAATGGCACGATCTTGGCTCGCTGCAACCTCCACCTCATGGGTTCAAGTTGAT A G NSD1 Ensembl:ENSG00000165671 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs895488656 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6376,RMVar_hsa_circ_109213,RMVar_hsa_circ_296651,RMVar_hsa_circ_322685,RMVar_hsa_circ_374749,RMVar_hsa_circ_236431,RMVar_hsa_circ_99866,RMVar_hsa_circ_236434,RMVar_hsa_circ_236435,RMVar_hsa_circ_236436,RMVar_hsa_circ_54322,RMVar_hsa_circ_325752,RMVar_hsa_circ_331791,RMVar_hsa_circ_97595,RMVar_hsa_circ_236437,RMVar_hsa_circ_236438 8711 RMVar_ID_8711 Human_SNP_ID_262919342 A-to-I Human chr5 + 177144051 177144051 177144051 TGATCGACCCACCTCGGCCTCCCAAAGTTGCTAGGATTACAGGTGTGAGCCATCTCTCCTGGCCA TGATCGACCCACCTCGGCCTCCCAAAGTTGCTGGGATTACAGGTGTGAGCCATCTCTCCTGGCCA A G NSD1 Ensembl:ENSG00000165671 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1252609208 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7420732 RMVar_hsa_circ_6376,RMVar_hsa_circ_109213,RMVar_hsa_circ_296651,RMVar_hsa_circ_322685,RMVar_hsa_circ_374749,RMVar_hsa_circ_236431,RMVar_hsa_circ_99866,RMVar_hsa_circ_236434,RMVar_hsa_circ_236435,RMVar_hsa_circ_236436,RMVar_hsa_circ_54322,RMVar_hsa_circ_325752,RMVar_hsa_circ_331791,RMVar_hsa_circ_97595,RMVar_hsa_circ_236437,RMVar_hsa_circ_236438 8712 RMVar_ID_8712 Human_SNP_ID_262919538 A-to-I Human chr5 + 177144824 177144824 177144824 TAATACTTGGCCGGGCGCGGTGGTTCACATCTATAATCCCAGCACTTTGGGAGGCTGAGGGGGTG TAATACTTGGCCGGGCGCGGTGGTTCACATCTGTAATCCCAGCACTTTGGGAGGCTGAGGGGGTG A G NSD1 Ensembl:ENSG00000165671 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1273086998 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6376,RMVar_hsa_circ_109213,RMVar_hsa_circ_296651,RMVar_hsa_circ_322685,RMVar_hsa_circ_374749,RMVar_hsa_circ_236431,RMVar_hsa_circ_99866,RMVar_hsa_circ_236434,RMVar_hsa_circ_236435,RMVar_hsa_circ_236436,RMVar_hsa_circ_54322,RMVar_hsa_circ_325752,RMVar_hsa_circ_331791,RMVar_hsa_circ_97595,RMVar_hsa_circ_236437,RMVar_hsa_circ_236438 8713 RMVar_ID_8713 Human_SNP_ID_262919546 A-to-I Human chr5 + 177144871 177144871 177144871 TGGGAGGCTGAGGGGGTGGATTATCTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACGTAGTGA TGGGAGGCTGAGGGGGTGGATTATCTGAGGTCCGGAGTTCAAGACCAGCCTGGCCAACGTAGTGA A C NSD1 Ensembl:ENSG00000165671 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1228495636 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25939791 RMVar_hsa_circ_6376,RMVar_hsa_circ_109213,RMVar_hsa_circ_296651,RMVar_hsa_circ_322685,RMVar_hsa_circ_374749,RMVar_hsa_circ_236431,RMVar_hsa_circ_99866,RMVar_hsa_circ_236434,RMVar_hsa_circ_236435,RMVar_hsa_circ_236436,RMVar_hsa_circ_54322,RMVar_hsa_circ_325752,RMVar_hsa_circ_331791,RMVar_hsa_circ_97595,RMVar_hsa_circ_236437,RMVar_hsa_circ_236438 8714 RMVar_ID_8714 Human_SNP_ID_262919547 A-to-I Human chr5 + 177144871 177144871 177144871 TGGGAGGCTGAGGGGGTGGATTATCTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACGTAGTGA TGGGAGGCTGAGGGGGTGGATTATCTGAGGTCGGGAGTTCAAGACCAGCCTGGCCAACGTAGTGA A G NSD1 Ensembl:ENSG00000165671 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1228495636 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25939791 RMVar_hsa_circ_6376,RMVar_hsa_circ_109213,RMVar_hsa_circ_296651,RMVar_hsa_circ_322685,RMVar_hsa_circ_374749,RMVar_hsa_circ_236431,RMVar_hsa_circ_99866,RMVar_hsa_circ_236434,RMVar_hsa_circ_236435,RMVar_hsa_circ_236436,RMVar_hsa_circ_54322,RMVar_hsa_circ_325752,RMVar_hsa_circ_331791,RMVar_hsa_circ_97595,RMVar_hsa_circ_236437,RMVar_hsa_circ_236438 8715 RMVar_ID_8715 Human_SNP_ID_262919706 A-to-I Human chr5 + 177145391 177145391 177145391 GTTTAGACCTCCTGTGTTAAAGTGATTCTCCTACTTTAGCCTCATGAGTAGTTGGGACTACAGGC GTTTAGACCTCCTGTGTTAAAGTGATTCTCCTGCTTTAGCCTCATGAGTAGTTGGGACTACAGGC A G NSD1 Ensembl:ENSG00000165671 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs974582814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15396505 RMVar_hsa_circ_6376,RMVar_hsa_circ_109213,RMVar_hsa_circ_296651,RMVar_hsa_circ_322685,RMVar_hsa_circ_374749,RMVar_hsa_circ_236431,RMVar_hsa_circ_99866,RMVar_hsa_circ_236434,RMVar_hsa_circ_236435,RMVar_hsa_circ_236436,RMVar_hsa_circ_54322,RMVar_hsa_circ_325752,RMVar_hsa_circ_331791,RMVar_hsa_circ_97595,RMVar_hsa_circ_236437,RMVar_hsa_circ_236438 8716 RMVar_ID_8716 Human_SNP_ID_262920254 A-to-I Human chr5 + 177147245 177147245 177147245 CTCCCACCTCAGCCTCCTGATTAGCTGCGACTACAGGCACTTGCCACCATGCCCCACTAATTTTT CTCCCACCTCAGCCTCCTGATTAGCTGCGACTGCAGGCACTTGCCACCATGCCCCACTAATTTTT A G NSD1 Ensembl:ENSG00000165671 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs76515674 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_42 RMVar_hsa_circ_6376,RMVar_hsa_circ_109213,RMVar_hsa_circ_296651,RMVar_hsa_circ_322685,RMVar_hsa_circ_374749,RMVar_hsa_circ_236431,RMVar_hsa_circ_99866,RMVar_hsa_circ_236434,RMVar_hsa_circ_236435,RMVar_hsa_circ_236436,RMVar_hsa_circ_54322,RMVar_hsa_circ_325752,RMVar_hsa_circ_331791,RMVar_hsa_circ_97595,RMVar_hsa_circ_236437,RMVar_hsa_circ_236438 8717 RMVar_ID_8717 Human_SNP_ID_262920279 A-to-I Human chr5 + 177147341 177147341 177147341 GTTGCTCAAGCTCGTCTTGAACTCGTGAGCTCAAGCAATCCGCCTGCCTTGGCCTCCCAAATGGC GTTGCTCAAGCTCGTCTTGAACTCGTGAGCTCGAGCAATCCGCCTGCCTTGGCCTCCCAAATGGC A G NSD1 Ensembl:ENSG00000165671 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs930139150 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15396527 RMVar_hsa_circ_6376,RMVar_hsa_circ_109213,RMVar_hsa_circ_296651,RMVar_hsa_circ_322685,RMVar_hsa_circ_374749,RMVar_hsa_circ_236431,RMVar_hsa_circ_99866,RMVar_hsa_circ_236434,RMVar_hsa_circ_236435,RMVar_hsa_circ_236436,RMVar_hsa_circ_54322,RMVar_hsa_circ_325752,RMVar_hsa_circ_331791,RMVar_hsa_circ_97595,RMVar_hsa_circ_236437,RMVar_hsa_circ_236438 8718 RMVar_ID_8718 Human_SNP_ID_262920987 A-to-I Human chr5 + 177149985 177149985 177149985 TTTTGAGACAGTCTTACTCTGTCACCCAGGCTAGAGTGCAATTGCGTGATCTTGGCACACTGCAA TTTTGAGACAGTCTTACTCTGTCACCCAGGCTTGAGTGCAATTGCGTGATCTTGGCACACTGCAA A T NSD1 Ensembl:ENSG00000165671 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs886731836 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15396665 RMVar_hsa_circ_6376,RMVar_hsa_circ_109213,RMVar_hsa_circ_296651,RMVar_hsa_circ_322685,RMVar_hsa_circ_374749,RMVar_hsa_circ_236431,RMVar_hsa_circ_99866,RMVar_hsa_circ_236434,RMVar_hsa_circ_236435,RMVar_hsa_circ_236436,RMVar_hsa_circ_54322,RMVar_hsa_circ_325752,RMVar_hsa_circ_331791,RMVar_hsa_circ_97595,RMVar_hsa_circ_236437,RMVar_hsa_circ_236438 8719 RMVar_ID_8719 Human_SNP_ID_262921288 A-to-I Human chr5 + 177151120 177151120 177151120 GAATTGCCAGCAGGGCACGGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCCTAGGCGGGA GAATTGCCAGCAGGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCTAGGCGGGA A G NSD1 Ensembl:ENSG00000165671 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1232617628 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15396690 RMVar_hsa_circ_6376,RMVar_hsa_circ_109213,RMVar_hsa_circ_296651,RMVar_hsa_circ_322685,RMVar_hsa_circ_374749,RMVar_hsa_circ_236431,RMVar_hsa_circ_99866,RMVar_hsa_circ_236434,RMVar_hsa_circ_236435,RMVar_hsa_circ_236436,RMVar_hsa_circ_54322,RMVar_hsa_circ_325752,RMVar_hsa_circ_331791,RMVar_hsa_circ_97595,RMVar_hsa_circ_236437,RMVar_hsa_circ_236438 8720 RMVar_ID_8720 Human_SNP_ID_262921410 A-to-I Human chr5 + 177151554 177151554 177151554 GGGATTACAGGCATGTGCCACCACGCCCGGCTAATTTTTGTATTTTTAGTAGAGATGGGATTTCT GGGATTACAGGCATGTGCCACCACGCCCGGCTGATTTTTGTATTTTTAGTAGAGATGGGATTTCT A G NSD1 Ensembl:ENSG00000165671 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs898147276 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6376,RMVar_hsa_circ_109213,RMVar_hsa_circ_296651,RMVar_hsa_circ_322685,RMVar_hsa_circ_374749,RMVar_hsa_circ_236431,RMVar_hsa_circ_99866,RMVar_hsa_circ_236434,RMVar_hsa_circ_236435,RMVar_hsa_circ_236436,RMVar_hsa_circ_54322,RMVar_hsa_circ_325752,RMVar_hsa_circ_331791,RMVar_hsa_circ_97595,RMVar_hsa_circ_236437,RMVar_hsa_circ_236438 8721 RMVar_ID_8721 Human_SNP_ID_262921444 A-to-I Human chr5 + 177151669 177151669 177151669 CCTCGGCTTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGTGCGTGTCCTTTTTTTTTTTTT CCTCGGCTTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGTGCGTGTCCTTTTTTTTTTTTT A G NSD1 Ensembl:ENSG00000165671 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs951654305 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6376,RMVar_hsa_circ_109213,RMVar_hsa_circ_296651,RMVar_hsa_circ_322685,RMVar_hsa_circ_374749,RMVar_hsa_circ_236431,RMVar_hsa_circ_99866,RMVar_hsa_circ_236434,RMVar_hsa_circ_236435,RMVar_hsa_circ_236436,RMVar_hsa_circ_54322,RMVar_hsa_circ_325752,RMVar_hsa_circ_331791,RMVar_hsa_circ_97595,RMVar_hsa_circ_236437,RMVar_hsa_circ_236438 8722 RMVar_ID_8722 Human_SNP_ID_262922412 A-to-I Human chr5 + 177155120 177155120 177155120 TCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCATGCCCCACCATGCTTG TCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTGGCTGGGACTACAGGCATGCCCCACCATGCTTG A G NSD1 Ensembl:ENSG00000165671 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1418145254 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6376,RMVar_hsa_circ_109213,RMVar_hsa_circ_296651,RMVar_hsa_circ_322685,RMVar_hsa_circ_374749,RMVar_hsa_circ_236431,RMVar_hsa_circ_99866,RMVar_hsa_circ_236434,RMVar_hsa_circ_236435,RMVar_hsa_circ_236436,RMVar_hsa_circ_54322,RMVar_hsa_circ_325752,RMVar_hsa_circ_331791,RMVar_hsa_circ_97595,RMVar_hsa_circ_236437,RMVar_hsa_circ_236438 8723 RMVar_ID_8723 Human_SNP_ID_262922432 A-to-I Human chr5 + 177155223 177155222 177155224 GTTGGTCAGGCTCGTGTCAAACTCCCTACCTCAGGGGATCCGCCCACCTTGGCCTCCCAAAGTGC GTTGGTCAGGCTCGTGTCAAACTCCCTACCTC__GGGATCCGCCCACCTTGGCCTCCCAAAGTGC CAG C NSD1 Ensembl:ENSG00000165671 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1491500588 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_15396819 RMVar_hsa_circ_6376,RMVar_hsa_circ_109213,RMVar_hsa_circ_296651,RMVar_hsa_circ_322685,RMVar_hsa_circ_374749,RMVar_hsa_circ_236431,RMVar_hsa_circ_99866,RMVar_hsa_circ_236434,RMVar_hsa_circ_236435,RMVar_hsa_circ_236436,RMVar_hsa_circ_54322,RMVar_hsa_circ_325752,RMVar_hsa_circ_331791,RMVar_hsa_circ_97595,RMVar_hsa_circ_236437,RMVar_hsa_circ_236438 8724 RMVar_ID_8724 Human_SNP_ID_262922433 A-to-I Human chr5 + 177155223 177155223 177155223 GTTGGTCAGGCTCGTGTCAAACTCCCTACCTCAGGGGATCCGCCCACCTTGGCCTCCCAAAGTGC GTTGGTCAGGCTCGTGTCAAACTCCCTACCTCCGGGGATCCGCCCACCTTGGCCTCCCAAAGTGC A C NSD1 Ensembl:ENSG00000165671 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1163984789 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15396819 RMVar_hsa_circ_6376,RMVar_hsa_circ_109213,RMVar_hsa_circ_296651,RMVar_hsa_circ_322685,RMVar_hsa_circ_374749,RMVar_hsa_circ_236431,RMVar_hsa_circ_99866,RMVar_hsa_circ_236434,RMVar_hsa_circ_236435,RMVar_hsa_circ_236436,RMVar_hsa_circ_54322,RMVar_hsa_circ_325752,RMVar_hsa_circ_331791,RMVar_hsa_circ_97595,RMVar_hsa_circ_236437,RMVar_hsa_circ_236438 8725 RMVar_ID_8725 Human_SNP_ID_262922972 A-to-I Human chr5 + 177157191 177157191 177157191 GGAGTTTGAGACCAGCCTGACCAACATGGTGAAACTTTGTCTCTACTAAAAATACAAAATTAGCT GGAGTTTGAGACCAGCCTGACCAACATGGTGATACTTTGTCTCTACTAAAAATACAAAATTAGCT A T NSD1 Ensembl:ENSG00000165671 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs941868442 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6376,RMVar_hsa_circ_109213,RMVar_hsa_circ_296651,RMVar_hsa_circ_322685,RMVar_hsa_circ_374749,RMVar_hsa_circ_236431,RMVar_hsa_circ_99866,RMVar_hsa_circ_236434,RMVar_hsa_circ_236435,RMVar_hsa_circ_236436,RMVar_hsa_circ_54322,RMVar_hsa_circ_325752,RMVar_hsa_circ_331791,RMVar_hsa_circ_97595,RMVar_hsa_circ_236437,RMVar_hsa_circ_236438 8726 RMVar_ID_8726 Human_SNP_ID_262922978 A-to-I Human chr5 + 177157212 177157212 177157212 CAACATGGTGAAACTTTGTCTCTACTAAAAATACAAAATTAGCTGGTGTGGTGGCGCATGGCTGT CAACATGGTGAAACTTTGTCTCTACTAAAAATTCAAAATTAGCTGGTGTGGTGGCGCATGGCTGT A T NSD1 Ensembl:ENSG00000165671 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs995851333 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6376,RMVar_hsa_circ_109213,RMVar_hsa_circ_296651,RMVar_hsa_circ_322685,RMVar_hsa_circ_374749,RMVar_hsa_circ_236431,RMVar_hsa_circ_99866,RMVar_hsa_circ_236434,RMVar_hsa_circ_236435,RMVar_hsa_circ_236436,RMVar_hsa_circ_54322,RMVar_hsa_circ_325752,RMVar_hsa_circ_331791,RMVar_hsa_circ_97595,RMVar_hsa_circ_236437,RMVar_hsa_circ_236438 8727 RMVar_ID_8727 Human_SNP_ID_262924661 A-to-I Human chr5 + 177161816 177161816 177161816 TTCTCCTCCTCTAGCCTCCTCCACGCCTGGCTAATATTTGTATTTTTAGTAGAGATGGGGTTTCA TTCTCCTCCTCTAGCCTCCTCCACGCCTGGCTGATATTTGTATTTTTAGTAGAGATGGGGTTTCA A G NSD1 Ensembl:ENSG00000165671 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1194222487 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6376,RMVar_hsa_circ_109213,RMVar_hsa_circ_296651,RMVar_hsa_circ_322685,RMVar_hsa_circ_374749,RMVar_hsa_circ_236431,RMVar_hsa_circ_99866,RMVar_hsa_circ_236434,RMVar_hsa_circ_236435,RMVar_hsa_circ_236436,RMVar_hsa_circ_54322,RMVar_hsa_circ_325752,RMVar_hsa_circ_331791,RMVar_hsa_circ_97595,RMVar_hsa_circ_236437,RMVar_hsa_circ_236438 8728 RMVar_ID_8728 Human_SNP_ID_262925409 A-to-I Human chr5 + 177164796 177164796 177164796 TGAAACTCCATCTCTACTAAAATACAAAAATTAGACCGGCATGGTGGCAGGTGCCTGTAATCCCA TGAAACTCCATCTCTACTAAAATACAAAAATTGGACCGGCATGGTGGCAGGTGCCTGTAATCCCA A G NSD1 Ensembl:ENSG00000165671 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1198756353 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6376,RMVar_hsa_circ_109213,RMVar_hsa_circ_296651,RMVar_hsa_circ_322685,RMVar_hsa_circ_374749,RMVar_hsa_circ_236431,RMVar_hsa_circ_99866,RMVar_hsa_circ_236434,RMVar_hsa_circ_236435,RMVar_hsa_circ_236436,RMVar_hsa_circ_54322,RMVar_hsa_circ_325752,RMVar_hsa_circ_331791,RMVar_hsa_circ_97595,RMVar_hsa_circ_236437,RMVar_hsa_circ_236438 8729 RMVar_ID_8729 Human_SNP_ID_262925611 A-to-I Human chr5 + 177165624 177165602 177165624 TCTTTTTCTTTCTCTTTTTGAGACAAGGTCTTACTCTGTTGCCCAGGCTAGAGTACAGTGGTGTG TCTTTTTCTTT______________________CTCTGTTGCCCAGGCTAGAGTACAGTGGTGTG TCTCTTTTTGAGACAAGGTCTTA T NSD1 Ensembl:ENSG00000165671 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs772973390 Functional Loss DEL dbSNP153 12..33 33 - - - RMVar_hsa_circ_6376,RMVar_hsa_circ_109213,RMVar_hsa_circ_296651,RMVar_hsa_circ_322685,RMVar_hsa_circ_374749,RMVar_hsa_circ_236431,RMVar_hsa_circ_99866,RMVar_hsa_circ_236434,RMVar_hsa_circ_236435,RMVar_hsa_circ_236436,RMVar_hsa_circ_54322,RMVar_hsa_circ_325752,RMVar_hsa_circ_331791,RMVar_hsa_circ_97595,RMVar_hsa_circ_236437,RMVar_hsa_circ_236438 8730 RMVar_ID_8730 Human_SNP_ID_262925618 A-to-I Human chr5 + 177165624 177165624 177165624 TCTTTTTCTTTCTCTTTTTGAGACAAGGTCTTACTCTGTTGCCCAGGCTAGAGTACAGTGGTGTG TCTTTTTCTTTCTCTTTTTGAGACAAGGTCTTTCTCTGTTGCCCAGGCTAGAGTACAGTGGTGTG A T NSD1 Ensembl:ENSG00000165671 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1462554998 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6376,RMVar_hsa_circ_109213,RMVar_hsa_circ_296651,RMVar_hsa_circ_322685,RMVar_hsa_circ_374749,RMVar_hsa_circ_236431,RMVar_hsa_circ_99866,RMVar_hsa_circ_236434,RMVar_hsa_circ_236435,RMVar_hsa_circ_236436,RMVar_hsa_circ_54322,RMVar_hsa_circ_325752,RMVar_hsa_circ_331791,RMVar_hsa_circ_97595,RMVar_hsa_circ_236437,RMVar_hsa_circ_236438 8731 RMVar_ID_8731 Human_SNP_ID_262925845 A-to-I Human chr5 + 177166427 177166427 177166427 AAAATTAGCCAAGTGTGGTGGCATGCACCTGTAGTCTGAGCTACTGGGGAGGCTGTGACAGGAGG AAAATTAGCCAAGTGTGGTGGCATGCACCTGTGGTCTGAGCTACTGGGGAGGCTGTGACAGGAGG A G NSD1 Ensembl:ENSG00000165671 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1347681513 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6376,RMVar_hsa_circ_109213,RMVar_hsa_circ_296651,RMVar_hsa_circ_322685,RMVar_hsa_circ_374749,RMVar_hsa_circ_236431,RMVar_hsa_circ_99866,RMVar_hsa_circ_236434,RMVar_hsa_circ_236435,RMVar_hsa_circ_236436,RMVar_hsa_circ_54322,RMVar_hsa_circ_325752,RMVar_hsa_circ_331791,RMVar_hsa_circ_97595,RMVar_hsa_circ_236437,RMVar_hsa_circ_236438 8732 RMVar_ID_8732 Human_SNP_ID_262927400 A-to-I Human chr5 + 177172237 177172237 177172237 TGCTAAAAATATTTTTGGATCCTGGATGTGGTAGTTCATGCCTATTATAATCCTAGCACTTTGGG TGCTAAAAATATTTTTGGATCCTGGATGTGGTGGTTCATGCCTATTATAATCCTAGCACTTTGGG A G NSD1 Ensembl:ENSG00000165671 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1308984126 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15397168 RMVar_hsa_circ_6376,RMVar_hsa_circ_109213,RMVar_hsa_circ_296651,RMVar_hsa_circ_322685,RMVar_hsa_circ_374749,RMVar_hsa_circ_236431,RMVar_hsa_circ_99866,RMVar_hsa_circ_236434,RMVar_hsa_circ_236435,RMVar_hsa_circ_236436,RMVar_hsa_circ_54322,RMVar_hsa_circ_325752,RMVar_hsa_circ_331791,RMVar_hsa_circ_97595,RMVar_hsa_circ_236437,RMVar_hsa_circ_236438 8733 RMVar_ID_8733 Human_SNP_ID_262927819 A-to-I Human chr5 + 177173673 177173673 177173673 TTTTGTATTTTTAGTAGAGACGGGATTTCCCCATGTTGGTCAGGCTGGTCTCGAACTTTTGACCT TTTTGTATTTTTAGTAGAGACGGGATTTCCCCCTGTTGGTCAGGCTGGTCTCGAACTTTTGACCT A C NSD1 Ensembl:ENSG00000165671 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971591403 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25882771 RMVar_hsa_circ_6376,RMVar_hsa_circ_109213,RMVar_hsa_circ_296651,RMVar_hsa_circ_322685,RMVar_hsa_circ_374749,RMVar_hsa_circ_236431,RMVar_hsa_circ_99866,RMVar_hsa_circ_236434,RMVar_hsa_circ_236435,RMVar_hsa_circ_236436,RMVar_hsa_circ_54322,RMVar_hsa_circ_325752,RMVar_hsa_circ_331791,RMVar_hsa_circ_97595,RMVar_hsa_circ_236437,RMVar_hsa_circ_236438 8734 RMVar_ID_8734 Human_SNP_ID_262927820 A-to-I Human chr5 + 177173673 177173673 177173673 TTTTGTATTTTTAGTAGAGACGGGATTTCCCCATGTTGGTCAGGCTGGTCTCGAACTTTTGACCT TTTTGTATTTTTAGTAGAGACGGGATTTCCCCGTGTTGGTCAGGCTGGTCTCGAACTTTTGACCT A G NSD1 Ensembl:ENSG00000165671 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971591403 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25882771 RMVar_hsa_circ_6376,RMVar_hsa_circ_109213,RMVar_hsa_circ_296651,RMVar_hsa_circ_322685,RMVar_hsa_circ_374749,RMVar_hsa_circ_236431,RMVar_hsa_circ_99866,RMVar_hsa_circ_236434,RMVar_hsa_circ_236435,RMVar_hsa_circ_236436,RMVar_hsa_circ_54322,RMVar_hsa_circ_325752,RMVar_hsa_circ_331791,RMVar_hsa_circ_97595,RMVar_hsa_circ_236437,RMVar_hsa_circ_236438 8735 RMVar_ID_8735 Human_SNP_ID_262927987 A-to-I Human chr5 + 177174211 177174211 177174211 ACATGGTGAAACCCCGTCTTTATTAAAAATACAAAAATTAGCAGGGCGTGGTGGTGCCCCAGCTA ACATGGTGAAACCCCGTCTTTATTAAAAATACGAAAATTAGCAGGGCGTGGTGGTGCCCCAGCTA A G NSD1 Ensembl:ENSG00000165671 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1225201408 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6376,RMVar_hsa_circ_109213,RMVar_hsa_circ_296651,RMVar_hsa_circ_322685,RMVar_hsa_circ_374749,RMVar_hsa_circ_236431,RMVar_hsa_circ_99866,RMVar_hsa_circ_236434,RMVar_hsa_circ_236435,RMVar_hsa_circ_236436,RMVar_hsa_circ_54322,RMVar_hsa_circ_325752,RMVar_hsa_circ_331791,RMVar_hsa_circ_97595,RMVar_hsa_circ_236437,RMVar_hsa_circ_236438 8736 RMVar_ID_8736 Human_SNP_ID_262928052 A-to-I Human chr5 + 177174402 177174401 177174403 GCCAAGCTAATTTTTGTGGTTTTAGTAGAGACAGGGCTTCGCCATGTTGGCCAGGCTGGTCTCGA GCCAAGCTAATTTTTGTGGTTTTAGTAGAGAC__GGCTTCGCCATGTTGGCCAGGCTGGTCTCGA CAG C NSD1 Ensembl:ENSG00000165671 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1046159749 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_6376,RMVar_hsa_circ_109213,RMVar_hsa_circ_296651,RMVar_hsa_circ_322685,RMVar_hsa_circ_374749,RMVar_hsa_circ_236431,RMVar_hsa_circ_99866,RMVar_hsa_circ_236434,RMVar_hsa_circ_236435,RMVar_hsa_circ_236436,RMVar_hsa_circ_54322,RMVar_hsa_circ_325752,RMVar_hsa_circ_331791,RMVar_hsa_circ_97595,RMVar_hsa_circ_236437,RMVar_hsa_circ_236438 8737 RMVar_ID_8737 Human_SNP_ID_262928053 A-to-I Human chr5 + 177174402 177174402 177174402 GCCAAGCTAATTTTTGTGGTTTTAGTAGAGACAGGGCTTCGCCATGTTGGCCAGGCTGGTCTCGA GCCAAGCTAATTTTTGTGGTTTTAGTAGAGACGGGGCTTCGCCATGTTGGCCAGGCTGGTCTCGA A G NSD1 Ensembl:ENSG00000165671 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1400923365 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6376,RMVar_hsa_circ_109213,RMVar_hsa_circ_296651,RMVar_hsa_circ_322685,RMVar_hsa_circ_374749,RMVar_hsa_circ_236431,RMVar_hsa_circ_99866,RMVar_hsa_circ_236434,RMVar_hsa_circ_236435,RMVar_hsa_circ_236436,RMVar_hsa_circ_54322,RMVar_hsa_circ_325752,RMVar_hsa_circ_331791,RMVar_hsa_circ_97595,RMVar_hsa_circ_236437,RMVar_hsa_circ_236438 8738 RMVar_ID_8738 Human_SNP_ID_262933675 A-to-I Human chr5 + 177194480 177194480 177194480 TTTTTTTTTTTGGGTGGAGATAGTGTCTCCATATATTACCCAGGCTGGTCTTGAAATCCTGAGCT TTTTTTTTTTTGGGTGGAGATAGTGTCTCCATGTATTACCCAGGCTGGTCTTGAAATCCTGAGCT A G NSD1 Ensembl:ENSG00000165671 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334242190 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10192,RMVar_hsa_circ_6376,RMVar_hsa_circ_109213,RMVar_hsa_circ_322685,RMVar_hsa_circ_374749,RMVar_hsa_circ_236431,RMVar_hsa_circ_99866,RMVar_hsa_circ_236435,RMVar_hsa_circ_236436,RMVar_hsa_circ_91848,RMVar_hsa_circ_54322,RMVar_hsa_circ_331791,RMVar_hsa_circ_97595,RMVar_hsa_circ_236437,RMVar_hsa_circ_236438,RMVar_hsa_circ_270806,RMVar_hsa_circ_291526,RMVar_hsa_circ_236440,RMVar_hsa_circ_376316,RMVar_hsa_circ_273157,RMVar_hsa_circ_69368,RMVar_hsa_circ_236441,RMVar_hsa_circ_236443,RMVar_hsa_circ_236444,RMVar_hsa_circ_236442 8739 RMVar_ID_8739 Human_SNP_ID_262935021 A-to-I Human chr5 + 177199648 177199648 177199648 TTTGAGATGGAGTCTCTCTCTGTCACCAGACTAGAGTGCAGTGGCACGATCTCAGCTCACTGCAA TTTGAGATGGAGTCTCTCTCTGTCACCAGACTGGAGTGCAGTGGCACGATCTCAGCTCACTGCAA A G NSD1 Ensembl:ENSG00000165671 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1255957960 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10192,RMVar_hsa_circ_6376,RMVar_hsa_circ_109213,RMVar_hsa_circ_322685,RMVar_hsa_circ_374749,RMVar_hsa_circ_236431,RMVar_hsa_circ_99866,RMVar_hsa_circ_236435,RMVar_hsa_circ_236436,RMVar_hsa_circ_91848,RMVar_hsa_circ_54322,RMVar_hsa_circ_331791,RMVar_hsa_circ_97595,RMVar_hsa_circ_236437,RMVar_hsa_circ_236438,RMVar_hsa_circ_270806,RMVar_hsa_circ_291526,RMVar_hsa_circ_236440,RMVar_hsa_circ_376316,RMVar_hsa_circ_273157,RMVar_hsa_circ_69368,RMVar_hsa_circ_236441,RMVar_hsa_circ_236443,RMVar_hsa_circ_236444,RMVar_hsa_circ_236442 8740 RMVar_ID_8740 Human_SNP_ID_262946668 A-to-I Human chr5 + 177243961 177243961 177243961 GTGATCCACCCGCCTCAGCCTCCTAACGTGCTAGGATTACAGGTGTGAGCCATCATGCCCTGTCT GTGATCCACCCGCCTCAGCCTCCTAACGTGCTGGGATTACAGGTGTGAGCCATCATGCCCTGTCT A G NSD1 Ensembl:ENSG00000165671 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs565924314 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28431,RMVar_hsa_circ_10192,RMVar_hsa_circ_6376,RMVar_hsa_circ_374749,RMVar_hsa_circ_99866,RMVar_hsa_circ_236435,RMVar_hsa_circ_236436,RMVar_hsa_circ_97595,RMVar_hsa_circ_236437,RMVar_hsa_circ_376316,RMVar_hsa_circ_69368,RMVar_hsa_circ_69580,RMVar_hsa_circ_236444,RMVar_hsa_circ_80082,RMVar_hsa_circ_348233,RMVar_hsa_circ_236448,RMVar_hsa_circ_365121,RMVar_hsa_circ_340710,RMVar_hsa_circ_83624,RMVar_hsa_circ_44396,RMVar_hsa_circ_236449,RMVar_hsa_circ_25478,RMVar_hsa_circ_236450,RMVar_hsa_circ_125340,RMVar_hsa_circ_40128,RMVar_hsa_circ_236453 8741 RMVar_ID_8741 Human_SNP_ID_262951365 A-to-I Human chr5 + 177262758 177262758 177262758 AAACTTAGCCAGGCGTGATGGCAGACACCTGTAATCCCAGCTACTTGGGAAGCTGAGGCAGGAGA AAACTTAGCCAGGCGTGATGGCAGACACCTGTCATCCCAGCTACTTGGGAAGCTGAGGCAGGAGA A C NSD1,AC146507.3 Ensembl:ENSG00000165671,Ensembl:ENSG00000286634 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903855556 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10192,RMVar_hsa_circ_6376,RMVar_hsa_circ_69368,RMVar_hsa_circ_80082,RMVar_hsa_circ_236448,RMVar_hsa_circ_83624,RMVar_hsa_circ_44396,RMVar_hsa_circ_236449,RMVar_hsa_circ_267839,RMVar_hsa_circ_40082,RMVar_hsa_circ_45716,RMVar_hsa_circ_267918,RMVar_hsa_circ_236457,RMVar_hsa_circ_269020,RMVar_hsa_circ_36072,RMVar_hsa_circ_50424,RMVar_hsa_circ_333428,RMVar_hsa_circ_22832 8742 RMVar_ID_8742 Human_SNP_ID_262955466 A-to-I Human chr5 + 177279224 177279224 177279224 AGTGCTTTTGCCAGGTGTGGTGGCTCACACCTATAATCCCAGCACTTTCAGAGACCGAGGCGGGC AGTGCTTTTGCCAGGTGTGGTGGCTCACACCTGTAATCCCAGCACTTTCAGAGACCGAGGCGGGC A G NSD1 Ensembl:ENSG00000165671 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1324315215 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83624,RMVar_hsa_circ_44396,RMVar_hsa_circ_236449,RMVar_hsa_circ_267839,RMVar_hsa_circ_40082,RMVar_hsa_circ_267918,RMVar_hsa_circ_269020,RMVar_hsa_circ_36072,RMVar_hsa_circ_50424,RMVar_hsa_circ_22832,RMVar_hsa_circ_236462,RMVar_hsa_circ_326597,RMVar_hsa_circ_339297,RMVar_hsa_circ_57504,RMVar_hsa_circ_296210,RMVar_hsa_circ_373986,RMVar_hsa_circ_281056,RMVar_hsa_circ_25592,RMVar_hsa_circ_236463,RMVar_hsa_circ_236464,RMVar_hsa_circ_325976,RMVar_hsa_circ_357405,RMVar_hsa_circ_40530,RMVar_hsa_circ_236466 8743 RMVar_ID_8743 Human_SNP_ID_262955504 A-to-I Human chr5 + 177279375 177279375 177279375 CAAAAATTAGCCGGGCTTGGTGGTGTGTGCCTATAGTCCCAGCTACCTGGGAGGCTGAGGCAGTA CAAAAATTAGCCGGGCTTGGTGGTGTGTGCCTTTAGTCCCAGCTACCTGGGAGGCTGAGGCAGTA A T NSD1 Ensembl:ENSG00000165671 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1006176966 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83624,RMVar_hsa_circ_44396,RMVar_hsa_circ_236449,RMVar_hsa_circ_267839,RMVar_hsa_circ_40082,RMVar_hsa_circ_267918,RMVar_hsa_circ_269020,RMVar_hsa_circ_36072,RMVar_hsa_circ_50424,RMVar_hsa_circ_22832,RMVar_hsa_circ_236462,RMVar_hsa_circ_326597,RMVar_hsa_circ_339297,RMVar_hsa_circ_57504,RMVar_hsa_circ_296210,RMVar_hsa_circ_373986,RMVar_hsa_circ_281056,RMVar_hsa_circ_25592,RMVar_hsa_circ_236463,RMVar_hsa_circ_236464,RMVar_hsa_circ_325976,RMVar_hsa_circ_357405,RMVar_hsa_circ_40530,RMVar_hsa_circ_236466 8744 RMVar_ID_8744 Human_SNP_ID_262967263 A-to-I Human chr5 - 177320880 177320880 177320880 AGTCTTGCTCTTGTTGCCTAGGCTTTAGTGCAATGGCACAGTCTTGGCTCATTGCAACCTCCGCC AGTCTTGCTCTTGTTGCCTAGGCTTTAGTGCAGTGGCACAGTCTTGGCTCATTGCAACCTCCGCC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs554507661 Functional Loss SNV dbSNP153 33..33 33 - - - 8745 RMVar_ID_8745 Human_SNP_ID_262968387 A-to-I Human chr5 - 177324264 177324264 177324264 GGAGGCCGAGGCACAAGGATTGCTTGAGCCTGAGAGGTTGAGGCTGCAGTGAGCTACGATCATGC GGAGGCCGAGGCACAAGGATTGCTTGAGCCTGGGAGGTTGAGGCTGCAGTGAGCTACGATCATGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1010857895 Functional Loss SNV dbSNP153 33..33 33 - - - 8746 RMVar_ID_8746 Human_SNP_ID_262968418 A-to-I Human chr5 - 177324373 177324373 177324373 AAGTGGTAGGATTGCTTGATCTCAGGAGTTCAAGACCAGCCTGGGCAACATTGTGAGACCCTGTC AAGTGGTAGGATTGCTTGATCTCAGGAGTTCAGGACCAGCCTGGGCAACATTGTGAGACCCTGTC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs951243018 Functional Loss SNV dbSNP153 33..33 33 - - - 8747 RMVar_ID_8747 Human_SNP_ID_262968419 A-to-I Human chr5 - 177324374 177324374 177324374 GAAGTGGTAGGATTGCTTGATCTCAGGAGTTCAAGACCAGCCTGGGCAACATTGTGAGACCCTGT GAAGTGGTAGGATTGCTTGATCTCAGGAGTTCGAGACCAGCCTGGGCAACATTGTGAGACCCTGT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs983043927 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25883497 8748 RMVar_ID_8748 Human_SNP_ID_262970829 A-to-I Human chr5 - 177331830 177331830 177331830 GGCTGGTGTCTCAGGAGCAGGGGTCTGTGTCTACAGATGGGCTGTGGCCCCTGCAGGCAGCTGTT GGCTGGTGTCTCAGGAGCAGGGGTCTGTGTCTTCAGATGGGCTGTGGCCCCTGCAGGCAGCTGTT T A LMAN2 Ensembl:ENSG00000169223 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1276339247 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_638878,Human_RBP_ID_1651303,Human_RBP_ID_7421446,Human_RBP_ID_17415461,Human_RBP_ID_24099092 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 8749 RMVar_ID_8749 Human_SNP_ID_262970830 A-to-I Human chr5 - 177331830 177331830 177331830 GGCTGGTGTCTCAGGAGCAGGGGTCTGTGTCTACAGATGGGCTGTGGCCCCTGCAGGCAGCTGTT GGCTGGTGTCTCAGGAGCAGGGGTCTGTGTCTGCAGATGGGCTGTGGCCCCTGCAGGCAGCTGTT T C LMAN2 Ensembl:ENSG00000169223 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1276339247 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_638878,Human_RBP_ID_1651303,Human_RBP_ID_7421446,Human_RBP_ID_17415461,Human_RBP_ID_24099092 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 8750 RMVar_ID_8750 Human_SNP_ID_262992043 A-to-I Human chr5 - 177404286 177404286 177404286 CCCAGGCGGCGCCTCCGACCCCGGTGTCCCCTAGGCTTCATGTCCCACTCATGCCCGCGCAGCCG CCCAGGCGGCGCCTCCGACCCCGGTGTCCCCTTGGCTTCATGTCCCACTCATGCCCGCGCAGCCG T A F12 Ensembl:ENSG00000131187 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs749549919 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_725003,Human_Splice_Rec_725011,Human_Splice_Rec_725035 Clinvar_Rec_43 RMVar_hsa_circ_98000,RMVar_hsa_circ_106089,RMVar_hsa_circ_236488,RMVar_hsa_circ_236489 8751 RMVar_ID_8751 Human_SNP_ID_263001265 A-to-I Human chr5 - 177438199 177438199 177438199 CATGCCCAGCTAATTTTGTATTTTTAGTAGAGATGGGGTTTCTCCATGTTGGTCAGGCTGGTCTT CATGCCCAGCTAATTTTGTATTTTTAGTAGAGGTGGGGTTTCTCCATGTTGGTCAGGCTGGTCTT T C PRR7-AS1,PRR7-AS1:2 RNACentral:URS000075BBA4,RNACentral:URS000075C7BA lincRNA,lincRNA exon,exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1045765045 Functional Loss SNV dbSNP153 33..33 33 - - - 8752 RMVar_ID_8752 Human_SNP_ID_263001267 A-to-I Human chr5 - 177438203 177438203 177438203 CCACCATGCCCAGCTAATTTTGTATTTTTAGTAGAGATGGGGTTTCTCCATGTTGGTCAGGCTGG CCACCATGCCCAGCTAATTTTGTATTTTTAGTGGAGATGGGGTTTCTCCATGTTGGTCAGGCTGG T C PRR7-AS1,PRR7-AS1:2 RNACentral:URS000075BBA4,RNACentral:URS000075C7BA lincRNA,lincRNA exon,exon GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs907317566 Functional Loss SNV dbSNP153 33..33 33 - - - 8753 RMVar_ID_8753 Human_SNP_ID_263001280 A-to-I Human chr5 + 177438257 177438257 177438257 GGGCATGGTGGCGCATGCCTGTAATCCCAGCTACTCGGCAGACTGAGGCAGGAGAATCGCTTGAA GGGCATGGTGGCGCATGCCTGTAATCCCAGCTTCTCGGCAGACTGAGGCAGGAGAATCGCTTGAA A T GRK6 Ensembl:ENSG00000198055 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1463044815 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76651,RMVar_hsa_circ_103816,RMVar_hsa_circ_91700,RMVar_hsa_circ_236491,RMVar_hsa_circ_106339,RMVar_hsa_circ_236492,RMVar_hsa_circ_236493,RMVar_hsa_circ_236497 8754 RMVar_ID_8754 Human_SNP_ID_263010299 A-to-I Human chr5 - 177467490 177467490 177467490 CACCGACTGCGGCTGCGAGAGGATGAGAACGCAGAGCCCGTGGTTAGTGTGTGTTTGGCACCCGT CACCGACTGCGGCTGCGAGAGGATGAGAACGCGGAGCCCGTGGTTAGTGTGTGTTTGGCACCCGT T C DBN1 Ensembl:ENSG00000113758 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs759205486 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250019 Human_Splice_Rec_725293,Human_Splice_Rec_725321,Human_Splice_Rec_725345,Human_Splice_Rec_725371,Human_Splice_Rec_725411,Human_Splice_Rec_725421 Human_miRNA_ID_2394795,Human_miRNA_ID_2394796,Human_miRNA_ID_3068415,Human_miRNA_ID_3068416 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_120179,RMVar_hsa_circ_236504,RMVar_hsa_circ_236505 8755 RMVar_ID_8755 Human_SNP_ID_263013464 A-to-I Human chr5 - 177477292 177477292 177477292 CTGCCTCAGCCTCCTGAGTAGCTGGGACTACAAGCATGCAACACCAGGCCCAGCTAATTTTTGTA CTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCATGCAACACCAGGCCCAGCTAATTTTTGTA T C AC145098.2 Ensembl:ENSG00000279821 Other exon GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1221878867 Functional Loss SNV dbSNP153 33..33 33 - - - 8756 RMVar_ID_8756 Human_SNP_ID_263015858 A-to-I Human chr5 - 177485793 177485793 177485793 TTTTGTAGAGATGAGGTTTTGCTATGTTGCCCAGGCTGGTCTCGAACTCCTGGCCTCGAGCGATC TTTTGTAGAGATGAGGTTTTGCTATGTTGCCCGGGCTGGTCTCGAACTCCTGGCCTCGAGCGATC T C PDLIM7 Ensembl:ENSG00000196923 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1021250013 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_319352,RMVar_hsa_circ_50409,RMVar_hsa_circ_236509 8757 RMVar_ID_8757 Human_SNP_ID_263015876 A-to-I Human chr5 - 177485870 177485870 177485870 AGGATCCTCCCACCTCAGCCTCCCAAATAGCTAGGACTAGAGGTGCCCACCAGCATGCTCAGCAG AGGATCCTCCCACCTCAGCCTCCCAAATAGCTGGGACTAGAGGTGCCCACCAGCATGCTCAGCAG T C PDLIM7 Ensembl:ENSG00000196923 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992239513 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_319352,RMVar_hsa_circ_50409,RMVar_hsa_circ_236509 8758 RMVar_ID_8758 Human_SNP_ID_263017282 A-to-I Human chr5 - 177489561 177489561 177489561 CTGGGCTGTGGACCCTGCGTTTGCCGAGCGCTATGCCCCGGACAAAACGAGCACAGTGCTGACCC CTGGGCTGTGGACCCTGCGTTTGCCGAGCGCTGTGCCCCGGACAAAACGAGCACAGTGCTGACCC T C PDLIM7 Ensembl:ENSG00000196923 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs377034000 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3967645,Human_RBP_ID_26352944 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 8759 RMVar_ID_8759 Human_SNP_ID_263017283 A-to-I Human chr5 - 177489561 177489561 177489561 CTGGGCTGTGGACCCTGCGTTTGCCGAGCGCTATGCCCCGGACAAAACGAGCACAGTGCTGACCC CTGGGCTGTGGACCCTGCGTTTGCCGAGCGCTCTGCCCCGGACAAAACGAGCACAGTGCTGACCC T G PDLIM7 Ensembl:ENSG00000196923 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs377034000 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3967645,Human_RBP_ID_26352944 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 8760 RMVar_ID_8760 Human_SNP_ID_263035689 A-to-I Human chr5 - 177550970 177550970 177550970 ATCAAAACTTAGCTGGGCATGGGTTCACACCTATAGTCTCAGCTAGTTGGGATGCTGAGGCGGGA ATCAAAACTTAGCTGGGCATGGGTTCACACCTGTAGTCTCAGCTAGTTGGGATGCTGAGGCGGGA T C FAM193B Ensembl:ENSG00000146067 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1431295319 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7421721 8761 RMVar_ID_8761 Human_SNP_ID_263052637 A-to-I Human chr5 + 177613394 177613394 177613394 GGCACCTGTAATCCCAGCTACTCGGGACGCCGAGGCAGGAGAATCGCTTGAACCCTAGAGGCAGA GGCACCTGTAATCCCAGCTACTCGGGACGCCGGGGCAGGAGAATCGCTTGAACCCTAGAGGCAGA A G AC139795.2 Ensembl:ENSG00000247679 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1308696776 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8268397,Human_RBP_ID_15401179 8762 RMVar_ID_8762 Human_SNP_ID_263087363 A-to-I Human chr5 - 177767358 177767358 177767358 TGCACACAAGTGTGCATAACTTTTTTGTGAAGATAGAGTCTTGCTGTTTCCCAAGCTGGCCTCAA TGCACACAAGTGTGCATAACTTTTTTGTGAAGGTAGAGTCTTGCTGTTTCCCAAGCTGGCCTCAA T C FAM153A Ensembl:ENSG00000170074 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1412764867 Functional Loss SNV dbSNP153 33..33 33 - - - 8763 RMVar_ID_8763 Human_SNP_ID_263125145 A-to-I Human chr5 + 177957972 177957972 177957972 GCTTGGCTAAGTTTTGTACTTTTTGTAGAGACAGGGTTTCGCCATGTTGCCCAGGCTAGTCTTGA GCTTGGCTAAGTTTTGTACTTTTTGTAGAGACGGGGTTTCGCCATGTTGCCCAGGCTAGTCTTGA A G AC106795.3,AC106795.2 Ensembl:ENSG00000250101,Ensembl:ENSG00000249684 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982197381 Functional Loss SNV dbSNP153 33..33 33 - - - 8764 RMVar_ID_8764 Human_SNP_ID_263125152 A-to-I Human chr5 + 177957992 177957992 177957992 TTTTGTAGAGACAGGGTTTCGCCATGTTGCCCAGGCTAGTCTTGAAATCCTGGACTCGAGATCTG TTTTGTAGAGACAGGGTTTCGCCATGTTGCCCGGGCTAGTCTTGAAATCCTGGACTCGAGATCTG A G AC106795.3,AC106795.2 Ensembl:ENSG00000250101,Ensembl:ENSG00000249684 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1398103272 Functional Loss SNV dbSNP153 33..33 33 - - - 8765 RMVar_ID_8765 Human_SNP_ID_263173777 A-to-I Human chr5 + 178132057 178132057 178132057 AGAATTGGCTGGGCACGGTGGTTCACGCCCGTAATTCCAGCACTTTGGGAGGCTGAGACTGGCAG AGAATTGGCTGGGCACGGTGGTTCACGCCCGTCATTCCAGCACTTTGGGAGGCTGAGACTGGCAG A C RMND5B Ensembl:ENSG00000145916 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1217329164 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_236560,RMVar_hsa_circ_122692 8766 RMVar_ID_8766 Human_SNP_ID_263173837 A-to-I Human chr5 + 178132320 178132320 178132320 AAATTTAGCCGGGTGTGGTGGCAGGTGTCTGTAATTCCAGCTACTTGGGAGGCTGAGGCAGGAGA AAATTTAGCCGGGTGTGGTGGCAGGTGTCTGTTATTCCAGCTACTTGGGAGGCTGAGGCAGGAGA A T RMND5B Ensembl:ENSG00000145916 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1464336273 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_236560,RMVar_hsa_circ_122692 8767 RMVar_ID_8767 Human_SNP_ID_263173840 A-to-I Human chr5 + 178132330 178132330 178132330 GGGTGTGGTGGCAGGTGTCTGTAATTCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAA GGGTGTGGTGGCAGGTGTCTGTAATTCCAGCTGCTTGGGAGGCTGAGGCAGGAGAATCGCTTGAA A G RMND5B Ensembl:ENSG00000145916 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs185760737 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_236560,RMVar_hsa_circ_122692 8768 RMVar_ID_8768 Human_SNP_ID_263174642 A-to-I Human chr5 + 178135179 178135179 178135179 TTTTGTTTTTTGTTTTTTTGAGACAGGGTCTCACTCTTGCTCAGGCTGGAATGCAGTGGCATAAT TTTTGTTTTTTGTTTTTTTGAGACAGGGTCTCTCTCTTGCTCAGGCTGGAATGCAGTGGCATAAT A T RMND5B Ensembl:ENSG00000145916 Protein coding 5'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941351971 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_727812 RMVar_hsa_circ_236560,RMVar_hsa_circ_122692 8769 RMVar_ID_8769 Human_SNP_ID_263174695 A-to-I Human chr5 + 178135267 178135267 178135267 TCCCGGGCTCAAGCAGTCCTCCGTCCCACCTCAGCCTTCTGAGGAGCTGGGACCACAGGCGTGTG TCCCGGGCTCAAGCAGTCCTCCGTCCCACCTCGGCCTTCTGAGGAGCTGGGACCACAGGCGTGTG A G RMND5B Ensembl:ENSG00000145916 Protein coding 5'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1448021478 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_727812,Human_Splice_Rec_727813,Human_Splice_Rec_727899 RMVar_hsa_circ_236560,RMVar_hsa_circ_122692 8770 RMVar_ID_8770 Human_SNP_ID_263174728 A-to-I Human chr5 + 178135385 178135385 178135385 AGCTCAGCAGTCTGCCTGCCTTGACCTCCCAAAATGCTGAGATTACAGGTGTGAGCCACTGCTCC AGCTCAGCAGTCTGCCTGCCTTGACCTCCCAAGATGCTGAGATTACAGGTGTGAGCCACTGCTCC A G RMND5B Ensembl:ENSG00000145916 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1206951302 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_236560,RMVar_hsa_circ_122692 8771 RMVar_ID_8771 Human_SNP_ID_263175163 A-to-I Human chr5 + 178137506 178137505 178137507 GCCCAGGAGTTTGAGACCAGCCAGGGCAACACAGAGAGACCCGTCTCTACGAAAAAAAATTTTAA GCCCAGGAGTTTGAGACCAGCCAGGGCAACAC__AGAGACCCGTCTCTACGAAAAAAAATTTTAA CAG C RMND5B Ensembl:ENSG00000145916 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982640675 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_236560,RMVar_hsa_circ_122692 8772 RMVar_ID_8772 Human_SNP_ID_263175589 A-to-I Human chr5 + 178138991 178138991 178138991 GGGAGCCCGAGGCCGACAGATCACCTGAGATCAGGAGTTTAAAACCAGCCTGGCCAACATGGCAA GGGAGCCCGAGGCCGACAGATCACCTGAGATCCGGAGTTTAAAACCAGCCTGGCCAACATGGCAA A C RMND5B Ensembl:ENSG00000145916 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1257346233 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_236560,RMVar_hsa_circ_122692 8773 RMVar_ID_8773 Human_SNP_ID_263176015 A-to-I Human chr5 + 178140597 178140597 178140597 GTGGGCTGTAATCCTAGCACTTTGGGAGGCTGAGGCGGGCGGATCACTCGAGCCCAGGAGGTTGA GTGGGCTGTAATCCTAGCACTTTGGGAGGCTGTGGCGGGCGGATCACTCGAGCCCAGGAGGTTGA A T RMND5B Ensembl:ENSG00000145916 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1420460839 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17575597 RMVar_hsa_circ_236560,RMVar_hsa_circ_122692 8774 RMVar_ID_8774 Human_SNP_ID_263177058 A-to-I Human chr5 + 178144473 178144473 178144473 AAAGTCCTTTAAGAAAAAAAAAAAGGCCAGGCACGGTGGCTCACGCCTGTAATCCCAATATTTTG AAAGTCCTTTAAGAAAAAAAAAAAGGCCAGGCGCGGTGGCTCACGCCTGTAATCCCAATATTTTG A G RMND5B Ensembl:ENSG00000145916 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6601219 Functional Loss SNV dbSNP153 33..33 33 - - - 8775 RMVar_ID_8775 Human_SNP_ID_263177076 A-to-I Human chr5 + 178144548 178144530 178144549 GTGGGCGGATCATGAGGTCCATCTTGGCTAACATGGTAAAACCCCATCTCTACTAAAAATACAAA GTGGGCGGATCATGA___________________GGTAAAACCCCATCTCTACTAAAAATACAAA AGGTCCATCTTGGCTAACAT A RMND5B Ensembl:ENSG00000145916 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1225948870 Functional Loss DEL dbSNP153 16..34 33 - - - 8776 RMVar_ID_8776 Human_SNP_ID_263177078 A-to-I Human chr5 + 178144545 178144545 178144545 GAGGTGGGCGGATCATGAGGTCCATCTTGGCTAACATGGTAAAACCCCATCTCTACTAAAAATAC GAGGTGGGCGGATCATGAGGTCCATCTTGGCTGACATGGTAAAACCCCATCTCTACTAAAAATAC A G RMND5B Ensembl:ENSG00000145916 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs35618073 Functional Loss SNV dbSNP153 33..33 33 - - - 8777 RMVar_ID_8777 Human_SNP_ID_263177242 A-to-I Human chr5 + 178145069 178145069 178145069 CCAAGCCATGATTTATTATTTATTTTTGAGACAAAGTCTCACTCTGTTGCCCAGGCTGGAGTGCA CCAAGCCATGATTTATTATTTATTTTTGAGACGAAGTCTCACTCTGTTGCCCAGGCTGGAGTGCA A G RMND5B Ensembl:ENSG00000145916 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1371177780 Functional Loss SNV dbSNP153 33..33 33 - - - 8778 RMVar_ID_8778 Human_SNP_ID_263177338 A-to-I Human chr5 + 178145431 178145431 178145431 TCACTTGAACCCGGGAAGCGGAGGCTGCAGTGAACCGAGATTGTGCCACTGCCCTCCAGCACTCC TCACTTGAACCCGGGAAGCGGAGGCTGCAGTGGACCGAGATTGTGCCACTGCCCTCCAGCACTCC A G RMND5B Ensembl:ENSG00000145916 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1561638937 Functional Loss SNV dbSNP153 33..33 33 - - - 8779 RMVar_ID_8779 Human_SNP_ID_263177415 A-to-I Human chr5 + 178145685 178145685 178145685 CCTTGGCCTCCCAAAGTGCTGGGATTATAGGCATGAGCCACCACGCCCGGCCCCAAAACATGACT CCTTGGCCTCCCAAAGTGCTGGGATTATAGGCCTGAGCCACCACGCCCGGCCCCAAAACATGACT A C RMND5B Ensembl:ENSG00000145916 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1253279266 Functional Loss SNV dbSNP153 33..33 33 - - - 8780 RMVar_ID_8780 Human_SNP_ID_263178810 A-to-I Human chr5 + 178150306 178150306 178150306 ACTATTTGGTTCTTACCATCAGGCCAAACGGTAAGTTCCTTCAGAACAGGGCCTCCTGCTTTATC ACTATTTGGTTCTTACCATCAGGCCAAACGGTTAGTTCCTTCAGAACAGGGCCTCCTGCTTTATC A T RMND5B Ensembl:ENSG00000145916 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031038391 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26529590 8781 RMVar_ID_8781 Human_SNP_ID_263188195 A-to-I Human chr5 + 178186072 178186072 178186072 TAGGTCAAAGCCGAAGTTAAAACCCGTCCAACACCAGTAGTATTCACCATCTTTGGCAAGCTTTC TAGGTCAAAGCCGAAGTTAAAACCCGTCCAACTCCAGTAGTATTCACCATCTTTGGCAAGCTTTC A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs758409804 Functional Loss SNV dbSNP153 33..33 33 - - - 8782 RMVar_ID_8782 Human_SNP_ID_263198284 A-to-I Human chr5 - 178217335 178217335 178217335 GCACCTATAGTCCCAGCTAGTTGGGAGGCTGAAGCACCAGAATCGCCTGAACCTGGGAGGCGGCA GCACCTATAGTCCCAGCTAGTTGGGAGGCTGAGGCACCAGAATCGCCTGAACCTGGGAGGCGGCA T C PHYKPL Ensembl:ENSG00000175309 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1561699010 Functional Loss SNV dbSNP153 33..33 33 - - - 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 8783 RMVar_ID_8783 Human_SNP_ID_263199185 A-to-I Human chr5 - 178220073 178220073 178220073 CCCCCACTTCAGCCTGCCAAGTACCTGGGACCACCGGTGCATGCTACCATGCCCAGCTAATTTTT CCCCCACTTCAGCCTGCCAAGTACCTGGGACCGCCGGTGCATGCTACCATGCCCAGCTAATTTTT T C PHYKPL Ensembl:ENSG00000175309 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs754170022 Functional Loss SNV dbSNP153 33..33 33 - - - 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 8784 RMVar_ID_8784 Human_SNP_ID_263199203 A-to-I Human chr5 - 178220143 178220143 178220143 TCACCCAGGCTGGAGTGCAGTGACGCGATCTCAGCTCACTGCAGCCTTTACTTCCAGAGCTCAAG TCACCCAGGCTGGAGTGCAGTGACGCGATCTCGGCTCACTGCAGCCTTTACTTCCAGAGCTCAAG T C PHYKPL Ensembl:ENSG00000175309 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1452432219 Functional Loss SNV dbSNP153 33..33 33 - - - 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 8785 RMVar_ID_8785 Human_SNP_ID_263199209 A-to-I Human chr5 - 178220153 178220153 178220153 TCTCACTCTGTCACCCAGGCTGGAGTGCAGTGACGCGATCTCAGCTCACTGCAGCCTTTACTTCC TCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGCGCGATCTCAGCTCACTGCAGCCTTTACTTCC T C PHYKPL Ensembl:ENSG00000175309 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1301153960 Functional Loss SNV dbSNP153 33..33 33 - - - 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 8786 RMVar_ID_8786 Human_SNP_ID_263306092 A-to-I Human chr5 - 178607796 178607796 178607796 AGAAAGTGTAGGTAGGGAGGGCCAGGCGGGGTAGCTCACACCTGTAATCCCAGCACTTTGGGAGG AGAAAGTGTAGGTAGGGAGGGCCAGGCGGGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGG T C CLK4 Ensembl:ENSG00000113240 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1377261033 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32386,RMVar_hsa_circ_236580,RMVar_hsa_circ_329233 8787 RMVar_ID_8787 Human_SNP_ID_263308270 A-to-I Human chr5 - 178616155 178616155 178616155 GGGGAGGAAGGCGGAGGTTGCGGTGAGCCAAGATTGTGCCATTGCACTCCAGCCTAGGCAACGAG GGGGAGGAAGGCGGAGGTTGCGGTGAGCCAAGGTTGTGCCATTGCACTCCAGCCTAGGCAACGAG T C CLK4 Ensembl:ENSG00000113240 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1039937742 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25884585 RMVar_hsa_circ_25948,RMVar_hsa_circ_236582,RMVar_hsa_circ_46901,RMVar_hsa_circ_40542,RMVar_hsa_circ_338035,RMVar_hsa_circ_26096 8788 RMVar_ID_8788 Human_SNP_ID_263562526 A-to-I Human chr5 - 179538947 179538945 179538947 ACCCAGGTAATTTTTGTATTTTTTGTAGAGACAGGGTTTCTCCATGTTGCCCAGGCTGGTCTCAA ACCCAGGTAATTTTTGTATTTTTTGTAGAGAC__GGTTTCTCCATGTTGCCCAGGCTGGTCTCAA CCT C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs774758738 Functional Loss DEL dbSNP153 33..34 33 - - - 8789 RMVar_ID_8789 Human_SNP_ID_263562527 A-to-I Human chr5 - 179538947 179538947 179538947 ACCCAGGTAATTTTTGTATTTTTTGTAGAGACAGGGTTTCTCCATGTTGCCCAGGCTGGTCTCAA ACCCAGGTAATTTTTGTATTTTTTGTAGAGACGGGGTTTCTCCATGTTGCCCAGGCTGGTCTCAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1185829842 Functional Loss SNV dbSNP153 33..33 33 - - - 8790 RMVar_ID_8790 Human_SNP_ID_263564174 A-to-I Human chr5 - 179545196 179545196 179545196 TTGTAGCGGACGGATTTCTTTGATTCAGGAGTAGAGACTAGCCTGGGCAACATGGTGAAAACCTA TTGTAGCGGACGGATTTCTTTGATTCAGGAGTGGAGACTAGCCTGGGCAACATGGTGAAAACCTA T C lnc-HNRNPH1-6 RNACentral:URS0000D594A1 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928462338 Functional Loss SNV dbSNP153 33..33 33 - - - 8791 RMVar_ID_8791 Human_SNP_ID_263570033 A-to-I Human chr5 + 179564596 179564596 179564596 TATAGGCTGAGGCAGGAGAATTGCCTGAACCCAGGAGGTGGAGGTTGCAGTGAGCAGAGATCACG TATAGGCTGAGGCAGGAGAATTGCCTGAACCCGGGAGGTGGAGGTTGCAGTGAGCAGAGATCACG A G RUFY1 Ensembl:ENSG00000176783 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232758589 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51768,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_37963 8792 RMVar_ID_8792 Human_SNP_ID_263570828 A-to-I Human chr5 + 179567513 179567513 179567513 GAGCGTGGCTTTATCTTGCACTCATGCAAAAGAAACTGGCAGATTATCTGAAAGTGCTTATAGAC GAGCGTGGCTTTATCTTGCACTCATGCAAAAGGAACTGGCAGATTATCTGAAAGTGCTTATAGAC A G RUFY1 Ensembl:ENSG00000176783 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1452067503 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_728962,Human_Splice_Rec_728963,Human_Splice_Rec_728996,Human_Splice_Rec_728997,Human_Splice_Rec_729028,Human_Splice_Rec_729029,Human_Splice_Rec_729038,Human_Splice_Rec_729039,Human_Splice_Rec_729072,Human_Splice_Rec_729073,Human_Splice_Rec_729102,Human_Splice_Rec_729104,Human_Splice_Rec_729105,Human_Splice_Rec_729119 RMVar_hsa_circ_51768,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 8793 RMVar_ID_8793 Human_SNP_ID_263574776 A-to-I Human chr5 + 179581750 179581750 179581750 TTGCCCAGGCTGAAGTGTAGTGGCGTGATCTCAGATCACTGTAGCCTCGAATTCCCAGGCTCAGG TTGCCCAGGCTGAAGTGTAGTGGCGTGATCTCGGATCACTGTAGCCTCGAATTCCCAGGCTCAGG A G RUFY1 Ensembl:ENSG00000176783 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1448462896 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15405693 RMVar_hsa_circ_341884,RMVar_hsa_circ_98089,RMVar_hsa_circ_37963,RMVar_hsa_circ_368590,RMVar_hsa_circ_71848,RMVar_hsa_circ_236609,RMVar_hsa_circ_17804,RMVar_hsa_circ_21667,RMVar_hsa_circ_296784,RMVar_hsa_circ_305306,RMVar_hsa_circ_355059,RMVar_hsa_circ_72913,RMVar_hsa_circ_327621,RMVar_hsa_circ_236613,RMVar_hsa_circ_17232,RMVar_hsa_circ_236612,RMVar_hsa_circ_357422,RMVar_hsa_circ_279925,RMVar_hsa_circ_310282,RMVar_hsa_circ_270284,RMVar_hsa_circ_236614,RMVar_hsa_circ_236615,RMVar_hsa_circ_236616 8794 RMVar_ID_8794 Human_SNP_ID_263574784 A-to-I Human chr5 + 179581774 179581774 179581774 GTGATCTCAGATCACTGTAGCCTCGAATTCCCAGGCTCAGGCAATTGATTCTCCCACCTCAGCCT GTGATCTCAGATCACTGTAGCCTCGAATTCCCGGGCTCAGGCAATTGATTCTCCCACCTCAGCCT A G RUFY1 Ensembl:ENSG00000176783 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935636932 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_341884,RMVar_hsa_circ_98089,RMVar_hsa_circ_37963,RMVar_hsa_circ_368590,RMVar_hsa_circ_71848,RMVar_hsa_circ_236609,RMVar_hsa_circ_17804,RMVar_hsa_circ_21667,RMVar_hsa_circ_296784,RMVar_hsa_circ_305306,RMVar_hsa_circ_355059,RMVar_hsa_circ_72913,RMVar_hsa_circ_327621,RMVar_hsa_circ_236613,RMVar_hsa_circ_17232,RMVar_hsa_circ_236612,RMVar_hsa_circ_357422,RMVar_hsa_circ_279925,RMVar_hsa_circ_310282,RMVar_hsa_circ_270284,RMVar_hsa_circ_236614,RMVar_hsa_circ_236615,RMVar_hsa_circ_236616 8795 RMVar_ID_8795 Human_SNP_ID_263574987 A-to-I Human chr5 + 179582633 179582633 179582633 CCAACACTTTGGGAGGCCGACGTGGGTGGATTACCTGAGGTTGGGAGTTCGAGACCAACATGGGG CCAACACTTTGGGAGGCCGACGTGGGTGGATTCCCTGAGGTTGGGAGTTCGAGACCAACATGGGG A C RUFY1 Ensembl:ENSG00000176783 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs957699124 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_341884,RMVar_hsa_circ_98089,RMVar_hsa_circ_37963,RMVar_hsa_circ_368590,RMVar_hsa_circ_71848,RMVar_hsa_circ_236609,RMVar_hsa_circ_17804,RMVar_hsa_circ_21667,RMVar_hsa_circ_296784,RMVar_hsa_circ_305306,RMVar_hsa_circ_355059,RMVar_hsa_circ_72913,RMVar_hsa_circ_327621,RMVar_hsa_circ_236613,RMVar_hsa_circ_17232,RMVar_hsa_circ_236612,RMVar_hsa_circ_357422,RMVar_hsa_circ_279925,RMVar_hsa_circ_310282,RMVar_hsa_circ_270284,RMVar_hsa_circ_236614,RMVar_hsa_circ_236615,RMVar_hsa_circ_236616 8796 RMVar_ID_8796 Human_SNP_ID_263577324 A-to-I Human chr5 + 179590884 179590884 179590884 TGGAAACAGAGTCTTGCTGTCACCCAGGCTGGAATGTAGTGGCGTGATCTTAGCTCACTGCAACC TGGAAACAGAGTCTTGCTGTCACCCAGGCTGGGATGTAGTGGCGTGATCTTAGCTCACTGCAACC A G RUFY1 Ensembl:ENSG00000176783 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1329675966 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_729130 RMVar_hsa_circ_2607,RMVar_hsa_circ_98089,RMVar_hsa_circ_236609,RMVar_hsa_circ_17804,RMVar_hsa_circ_21667,RMVar_hsa_circ_296784,RMVar_hsa_circ_305306,RMVar_hsa_circ_72913,RMVar_hsa_circ_327621,RMVar_hsa_circ_236613,RMVar_hsa_circ_17232,RMVar_hsa_circ_236612,RMVar_hsa_circ_357422,RMVar_hsa_circ_279925,RMVar_hsa_circ_310282,RMVar_hsa_circ_68206,RMVar_hsa_circ_236614,RMVar_hsa_circ_236615,RMVar_hsa_circ_267810,RMVar_hsa_circ_358727,RMVar_hsa_circ_276018,RMVar_hsa_circ_113063,RMVar_hsa_circ_236618,RMVar_hsa_circ_17168,RMVar_hsa_circ_236617,RMVar_hsa_circ_301410,RMVar_hsa_circ_236620,RMVar_hsa_circ_236619 8797 RMVar_ID_8797 Human_SNP_ID_263577356 A-to-I Human chr5 + 179591023 179591022 179591024 ACCCGACTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGTGTCAA ACCCGACTAATTTTTGTATTTTTAGTAGAGAC__GGTTTCACCATGTTGGCCAGGCTGGTGTCAA CAG C RUFY1 Ensembl:ENSG00000176783 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1211149831 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_2607,RMVar_hsa_circ_98089,RMVar_hsa_circ_236609,RMVar_hsa_circ_17804,RMVar_hsa_circ_21667,RMVar_hsa_circ_296784,RMVar_hsa_circ_305306,RMVar_hsa_circ_72913,RMVar_hsa_circ_327621,RMVar_hsa_circ_236613,RMVar_hsa_circ_17232,RMVar_hsa_circ_236612,RMVar_hsa_circ_357422,RMVar_hsa_circ_279925,RMVar_hsa_circ_310282,RMVar_hsa_circ_68206,RMVar_hsa_circ_236614,RMVar_hsa_circ_236615,RMVar_hsa_circ_267810,RMVar_hsa_circ_358727,RMVar_hsa_circ_276018,RMVar_hsa_circ_113063,RMVar_hsa_circ_236618,RMVar_hsa_circ_17168,RMVar_hsa_circ_236617,RMVar_hsa_circ_301410,RMVar_hsa_circ_236620,RMVar_hsa_circ_236619 8798 RMVar_ID_8798 Human_SNP_ID_263577377 A-to-I Human chr5 + 179591113 179591113 179591113 CCTTGGCCTTCCAAAGTGCTGGGATTACAGGCATGAGCCACCACACCCAGCCTATGAACTTAACT CCTTGGCCTTCCAAAGTGCTGGGATTACAGGCGTGAGCCACCACACCCAGCCTATGAACTTAACT A G RUFY1 Ensembl:ENSG00000176783 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1163744941 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2607,RMVar_hsa_circ_98089,RMVar_hsa_circ_236609,RMVar_hsa_circ_17804,RMVar_hsa_circ_21667,RMVar_hsa_circ_296784,RMVar_hsa_circ_305306,RMVar_hsa_circ_72913,RMVar_hsa_circ_327621,RMVar_hsa_circ_236613,RMVar_hsa_circ_17232,RMVar_hsa_circ_236612,RMVar_hsa_circ_357422,RMVar_hsa_circ_279925,RMVar_hsa_circ_310282,RMVar_hsa_circ_68206,RMVar_hsa_circ_236614,RMVar_hsa_circ_236615,RMVar_hsa_circ_267810,RMVar_hsa_circ_358727,RMVar_hsa_circ_276018,RMVar_hsa_circ_113063,RMVar_hsa_circ_236618,RMVar_hsa_circ_17168,RMVar_hsa_circ_236617,RMVar_hsa_circ_301410,RMVar_hsa_circ_236620,RMVar_hsa_circ_236619 8799 RMVar_ID_8799 Human_SNP_ID_263577432 A-to-I Human chr5 + 179591246 179591246 179591246 TTGCCCTGTCGCCCAGGCTGGAGTGCAATGGCACGATCTTGGCTCACTGCAAGCTCTGCCTCCCG TTGCCCTGTCGCCCAGGCTGGAGTGCAATGGCGCGATCTTGGCTCACTGCAAGCTCTGCCTCCCG A G RUFY1 Ensembl:ENSG00000176783 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1422354160 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2607,RMVar_hsa_circ_98089,RMVar_hsa_circ_236609,RMVar_hsa_circ_17804,RMVar_hsa_circ_21667,RMVar_hsa_circ_296784,RMVar_hsa_circ_305306,RMVar_hsa_circ_72913,RMVar_hsa_circ_327621,RMVar_hsa_circ_236613,RMVar_hsa_circ_17232,RMVar_hsa_circ_236612,RMVar_hsa_circ_357422,RMVar_hsa_circ_279925,RMVar_hsa_circ_310282,RMVar_hsa_circ_68206,RMVar_hsa_circ_236614,RMVar_hsa_circ_236615,RMVar_hsa_circ_267810,RMVar_hsa_circ_358727,RMVar_hsa_circ_276018,RMVar_hsa_circ_113063,RMVar_hsa_circ_236618,RMVar_hsa_circ_17168,RMVar_hsa_circ_236617,RMVar_hsa_circ_301410,RMVar_hsa_circ_236620,RMVar_hsa_circ_236619 8800 RMVar_ID_8800 Human_SNP_ID_263578329 A-to-I Human chr5 + 179594041 179594041 179594041 AAGACGTCATTTAGAGCCAGGCACGGTGGCTCACGCTTGTAATCCCAGCACTTTGGGAGGCCGAG AAGACGTCATTTAGAGCCAGGCACGGTGGCTCCCGCTTGTAATCCCAGCACTTTGGGAGGCCGAG A C RUFY1 Ensembl:ENSG00000176783 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1433495658 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2607,RMVar_hsa_circ_98089,RMVar_hsa_circ_236609,RMVar_hsa_circ_17804,RMVar_hsa_circ_305306,RMVar_hsa_circ_72913,RMVar_hsa_circ_327621,RMVar_hsa_circ_236613,RMVar_hsa_circ_17232,RMVar_hsa_circ_357422,RMVar_hsa_circ_310282,RMVar_hsa_circ_68206,RMVar_hsa_circ_236614,RMVar_hsa_circ_267810,RMVar_hsa_circ_113063,RMVar_hsa_circ_236618,RMVar_hsa_circ_17168,RMVar_hsa_circ_236620,RMVar_hsa_circ_356535,RMVar_hsa_circ_366685,RMVar_hsa_circ_301800,RMVar_hsa_circ_236622,RMVar_hsa_circ_362721,RMVar_hsa_circ_314006 8801 RMVar_ID_8801 Human_SNP_ID_263578474 A-to-I Human chr5 + 179594500 179594499 179594500 AAACAGCATCTAGTCCGGGCGTGGTGGCTCACACCTGTAATCCCAGCACTCTGGGAGGCCAAGGC AAACAGCATCTAGTCCGGGCGTGGTGGCTCATGCCTGTAATCCCAGCACTCTGGGAGGCCAAGGC CA TG RUFY1 Ensembl:ENSG00000176783 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs386695646 Functional Loss MNV dbSNP153 32..33 33 - - - RMVar_hsa_circ_2607,RMVar_hsa_circ_98089,RMVar_hsa_circ_236609,RMVar_hsa_circ_17804,RMVar_hsa_circ_305306,RMVar_hsa_circ_72913,RMVar_hsa_circ_327621,RMVar_hsa_circ_236613,RMVar_hsa_circ_17232,RMVar_hsa_circ_357422,RMVar_hsa_circ_310282,RMVar_hsa_circ_68206,RMVar_hsa_circ_236614,RMVar_hsa_circ_267810,RMVar_hsa_circ_113063,RMVar_hsa_circ_236618,RMVar_hsa_circ_17168,RMVar_hsa_circ_236620,RMVar_hsa_circ_356535,RMVar_hsa_circ_366685,RMVar_hsa_circ_301800,RMVar_hsa_circ_236622,RMVar_hsa_circ_362721,RMVar_hsa_circ_314006 8802 RMVar_ID_8802 Human_SNP_ID_263578477 A-to-I Human chr5 + 179594500 179594500 179594500 AAACAGCATCTAGTCCGGGCGTGGTGGCTCACACCTGTAATCCCAGCACTCTGGGAGGCCAAGGC AAACAGCATCTAGTCCGGGCGTGGTGGCTCACGCCTGTAATCCCAGCACTCTGGGAGGCCAAGGC A G RUFY1 Ensembl:ENSG00000176783 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1259582046 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2607,RMVar_hsa_circ_98089,RMVar_hsa_circ_236609,RMVar_hsa_circ_17804,RMVar_hsa_circ_305306,RMVar_hsa_circ_72913,RMVar_hsa_circ_327621,RMVar_hsa_circ_236613,RMVar_hsa_circ_17232,RMVar_hsa_circ_357422,RMVar_hsa_circ_310282,RMVar_hsa_circ_68206,RMVar_hsa_circ_236614,RMVar_hsa_circ_267810,RMVar_hsa_circ_113063,RMVar_hsa_circ_236618,RMVar_hsa_circ_17168,RMVar_hsa_circ_236620,RMVar_hsa_circ_356535,RMVar_hsa_circ_366685,RMVar_hsa_circ_301800,RMVar_hsa_circ_236622,RMVar_hsa_circ_362721,RMVar_hsa_circ_314006 8803 RMVar_ID_8803 Human_SNP_ID_263578481 A-to-I Human chr5 + 179594506 179594506 179594506 CATCTAGTCCGGGCGTGGTGGCTCACACCTGTAATCCCAGCACTCTGGGAGGCCAAGGCAGGCGG CATCTAGTCCGGGCGTGGTGGCTCACACCTGTTATCCCAGCACTCTGGGAGGCCAAGGCAGGCGG A T RUFY1 Ensembl:ENSG00000176783 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1316933116 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2607,RMVar_hsa_circ_98089,RMVar_hsa_circ_236609,RMVar_hsa_circ_17804,RMVar_hsa_circ_305306,RMVar_hsa_circ_72913,RMVar_hsa_circ_327621,RMVar_hsa_circ_236613,RMVar_hsa_circ_17232,RMVar_hsa_circ_357422,RMVar_hsa_circ_310282,RMVar_hsa_circ_68206,RMVar_hsa_circ_236614,RMVar_hsa_circ_267810,RMVar_hsa_circ_113063,RMVar_hsa_circ_236618,RMVar_hsa_circ_17168,RMVar_hsa_circ_236620,RMVar_hsa_circ_356535,RMVar_hsa_circ_366685,RMVar_hsa_circ_301800,RMVar_hsa_circ_236622,RMVar_hsa_circ_362721,RMVar_hsa_circ_314006 8804 RMVar_ID_8804 Human_SNP_ID_263591076 A-to-I Human chr5 - 179630016 179630016 179630016 CAGGGTTCTGTTTTTTTGTTTTATTTTGAGACAGAGTCGTTCTGTCACCGAGGCTCGAGTGTAGT CAGGGTTCTGTTTTTTTGTTTTATTTTGAGACTGAGTCGTTCTGTCACCGAGGCTCGAGTGTAGT T A HNRNPH1 Ensembl:ENSG00000169045 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1460218384 Functional Loss SNV dbSNP153 33..33 33 - - - 8805 RMVar_ID_8805 Human_SNP_ID_263592026 A-to-I Human chr5 - 179632828 179632828 179632828 AAAAAAAAATTCGCCGGGCTTGGTGGGGCTGTAATCCCACCTACTCGGGAAGCTGAGCCTGGGCA AAAAAAAAATTCGCCGGGCTTGGTGGGGCTGTTATCCCACCTACTCGGGAAGCTGAGCCTGGGCA T A HNRNPH1 Ensembl:ENSG00000169045 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1240474010 Functional Loss SNV dbSNP153 33..33 33 - - - 8806 RMVar_ID_8806 Human_SNP_ID_263603745 A-to-I Human chr5 + 179675124 179675124 179675124 TTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCAGGTCTCGAACTCCTGACCT TTTTGTATTTTTAGTAGAGACGGGGTTTCACCGTGTTGGCCAGGCAGGTCTCGAACTCCTGACCT A G LOC105377763,LOC105377763:2 RNACentral:URS00008BC9FD,RNACentral:URS0000D57322 lincRNA,lincRNA exon,intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1028781155 Functional Loss SNV dbSNP153 33..33 33 - - - 8807 RMVar_ID_8807 Human_SNP_ID_263604570 A-to-I Human chr5 - 179677872 179677872 179677872 TGGCTCACTGCAACCTCGAGCTTCCGGGCTCAAGCAGTCCTCCCACCTCAGCCTCCCAAACGTGG TGGCTCACTGCAACCTCGAGCTTCCGGGCTCAGGCAGTCCTCCCACCTCAGCCTCCCAAACGTGG T C lnc-CBY3-1 RNACentral:URS0000D5B916 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1237594537 Functional Loss SNV dbSNP153 33..33 33 - - - 8808 RMVar_ID_8808 Human_SNP_ID_263610248 A-to-I Human chr5 + 179697077 179697077 179697077 CATCTGTTTGTTTTTATTATTTATTTATTTAGAGACGGGTTCTCACTCTGTTGCCCAGGCTGGAT CATCTGTTTGTTTTTATTATTTATTTATTTAGGGACGGGTTCTCACTCTGTTGCCCAGGCTGGAT A G CANX Ensembl:ENSG00000127022 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1291444543 Functional Loss SNV dbSNP153 33..33 33 - - - 8809 RMVar_ID_8809 Human_SNP_ID_263611631 A-to-I Human chr5 + 179701497 179701497 179701497 GGAGGCTGAGGCAGGAGAATCACTAAACCTGGAAGGCGGAGGTTGCAGTGAGCGGAGATGGTTCC GGAGGCTGAGGCAGGAGAATCACTAAACCTGGGAGGCGGAGGTTGCAGTGAGCGGAGATGGTTCC A G CANX Ensembl:ENSG00000127022 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1247858727 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_236643,RMVar_hsa_circ_113904 8810 RMVar_ID_8810 Human_SNP_ID_263612464 A-to-I Human chr5 + 179704316 179704315 179704317 TTGGAAGGCCGAGGCGGGCAGATCACGACGTCAAGAGATTGAGACTATCCTGGCCAACACGGTGA TTGGAAGGCCGAGGCGGGCAGATCACGACGTC__GAGATTGAGACTATCCTGGCCAACACGGTGA CAA C CANX Ensembl:ENSG00000127022 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1386510747 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_236643,RMVar_hsa_circ_113904,RMVar_hsa_circ_353701 8811 RMVar_ID_8811 Human_SNP_ID_263612472 A-to-I Human chr5 + 179704374 179704374 179704374 ACGGTGAAACCCTGTCTCTATTAAAAATAACAAAAATTAGCTGGATGTGGTGGTGCACACCTGTC ACGGTGAAACCCTGTCTCTATTAAAAATAACAGAAATTAGCTGGATGTGGTGGTGCACACCTGTC A G CANX Ensembl:ENSG00000127022 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1015540719 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15407788 Human_Splice_Rec_729839 RMVar_hsa_circ_236643,RMVar_hsa_circ_113904,RMVar_hsa_circ_353701 8812 RMVar_ID_8812 Human_SNP_ID_263612476 A-to-I Human chr5 + 179704407 179704407 179704407 AAATTAGCTGGATGTGGTGGTGCACACCTGTCATCCCACCTACTTGGGAGGCTGAGGTAGGAGAA AAATTAGCTGGATGTGGTGGTGCACACCTGTCGTCCCACCTACTTGGGAGGCTGAGGTAGGAGAA A G CANX Ensembl:ENSG00000127022 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1467835681 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_729839 RMVar_hsa_circ_236643,RMVar_hsa_circ_113904,RMVar_hsa_circ_353701 8813 RMVar_ID_8813 Human_SNP_ID_263613272 A-to-I Human chr5 + 179707401 179707401 179707401 GGTCAGGAGATCGAGACCATCCTGGCTAACACAGTGAAACCCCGTCTCTACTGAAAATACAAAAA GGTCAGGAGATCGAGACCATCCTGGCTAACACGGTGAAACCCCGTCTCTACTGAAAATACAAAAA A G CANX Ensembl:ENSG00000127022 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs549706870 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5155,RMVar_hsa_circ_314002,RMVar_hsa_circ_358735,RMVar_hsa_circ_328988,RMVar_hsa_circ_292291,RMVar_hsa_circ_309008,RMVar_hsa_circ_282791,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_319738,RMVar_hsa_circ_358280,RMVar_hsa_circ_373278,RMVar_hsa_circ_61838,RMVar_hsa_circ_97640,RMVar_hsa_circ_236652,RMVar_hsa_circ_236653,RMVar_hsa_circ_306201,RMVar_hsa_circ_359776,RMVar_hsa_circ_365352,RMVar_hsa_circ_310809,RMVar_hsa_circ_296681,RMVar_hsa_circ_236654,RMVar_hsa_circ_236656,RMVar_hsa_circ_236657,RMVar_hsa_circ_236655 8814 RMVar_ID_8814 Human_SNP_ID_263614078 A-to-I Human chr5 + 179710198 179710198 179710198 TAATCCCAGCACTTTGGGAGGCCGAGATGGGCAGATCACCTGAGATCAGGAATTCGAGAACAGTC TAATCCCAGCACTTTGGGAGGCCGAGATGGGCGGATCACCTGAGATCAGGAATTCGAGAACAGTC A G CANX Ensembl:ENSG00000127022 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1283016657 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15407914 RMVar_hsa_circ_358735,RMVar_hsa_circ_328988,RMVar_hsa_circ_309008,RMVar_hsa_circ_282791,RMVar_hsa_circ_277193,RMVar_hsa_circ_236650,RMVar_hsa_circ_236651,RMVar_hsa_circ_236649,RMVar_hsa_circ_358280,RMVar_hsa_circ_373278,RMVar_hsa_circ_74601,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_283752,RMVar_hsa_circ_16635,RMVar_hsa_circ_306623,RMVar_hsa_circ_342219,RMVar_hsa_circ_278860,RMVar_hsa_circ_280622,RMVar_hsa_circ_270449,RMVar_hsa_circ_236662,RMVar_hsa_circ_236664,RMVar_hsa_circ_236665,RMVar_hsa_circ_236666,RMVar_hsa_circ_236663 8815 RMVar_ID_8815 Human_SNP_ID_263614104 A-to-I Human chr5 + 179710280 179710280 179710280 CTTCACCTCTACTAAAAATACAAATATTAGCTAGGCATGGTGGTGCACGCCTGTAACCGAAGCTA CTTCACCTCTACTAAAAATACAAATATTAGCTGGGCATGGTGGTGCACGCCTGTAACCGAAGCTA A G CANX Ensembl:ENSG00000127022 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1442191183 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_358735,RMVar_hsa_circ_328988,RMVar_hsa_circ_309008,RMVar_hsa_circ_282791,RMVar_hsa_circ_277193,RMVar_hsa_circ_236650,RMVar_hsa_circ_236651,RMVar_hsa_circ_236649,RMVar_hsa_circ_358280,RMVar_hsa_circ_373278,RMVar_hsa_circ_74601,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_283752,RMVar_hsa_circ_16635,RMVar_hsa_circ_306623,RMVar_hsa_circ_342219,RMVar_hsa_circ_278860,RMVar_hsa_circ_280622,RMVar_hsa_circ_270449,RMVar_hsa_circ_236662,RMVar_hsa_circ_236664,RMVar_hsa_circ_236665,RMVar_hsa_circ_236666,RMVar_hsa_circ_236663 8816 RMVar_ID_8816 Human_SNP_ID_263614418 A-to-I Human chr5 + 179711162 179711162 179711162 AAGAAGCTTCTTGGCCACGTATGGTGGCCCACACCTGTAATCCTAACACTTCGGGAGGCTGAATC AAGAAGCTTCTTGGCCACGTATGGTGGCCCACGCCTGTAATCCTAACACTTCGGGAGGCTGAATC A G CANX Ensembl:ENSG00000127022 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs906047727 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_358735,RMVar_hsa_circ_328988,RMVar_hsa_circ_309008,RMVar_hsa_circ_282791,RMVar_hsa_circ_277193,RMVar_hsa_circ_236650,RMVar_hsa_circ_236651,RMVar_hsa_circ_236649,RMVar_hsa_circ_358280,RMVar_hsa_circ_373278,RMVar_hsa_circ_74601,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_283752,RMVar_hsa_circ_16635,RMVar_hsa_circ_306623,RMVar_hsa_circ_342219,RMVar_hsa_circ_278860,RMVar_hsa_circ_280622,RMVar_hsa_circ_270449,RMVar_hsa_circ_236662,RMVar_hsa_circ_236664,RMVar_hsa_circ_236665,RMVar_hsa_circ_236666,RMVar_hsa_circ_236663 8817 RMVar_ID_8817 Human_SNP_ID_263614520 A-to-I Human chr5 + 179711531 179711531 179711531 GTGTTTTTGGCCAGGCATGGTGGCTCGTGCCTATAATCCCAGCACTTTGGGTGGCCGAGGTGGGC GTGTTTTTGGCCAGGCATGGTGGCTCGTGCCTGTAATCCCAGCACTTTGGGTGGCCGAGGTGGGC A G CANX Ensembl:ENSG00000127022 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1028732446 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_358735,RMVar_hsa_circ_328988,RMVar_hsa_circ_309008,RMVar_hsa_circ_282791,RMVar_hsa_circ_277193,RMVar_hsa_circ_236650,RMVar_hsa_circ_236651,RMVar_hsa_circ_236649,RMVar_hsa_circ_358280,RMVar_hsa_circ_373278,RMVar_hsa_circ_74601,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_283752,RMVar_hsa_circ_16635,RMVar_hsa_circ_306623,RMVar_hsa_circ_342219,RMVar_hsa_circ_278860,RMVar_hsa_circ_280622,RMVar_hsa_circ_270449,RMVar_hsa_circ_236662,RMVar_hsa_circ_236664,RMVar_hsa_circ_236665,RMVar_hsa_circ_236666,RMVar_hsa_circ_236663 8818 RMVar_ID_8818 Human_SNP_ID_263614589 A-to-I Human chr5 + 179711770 179711770 179711770 AGATTGTGACACTGCACTCCAGCCTGGGCGACAGGAAGACTCTGTCTCAAAAAAAAAAAAAAAAA AGATTGTGACACTGCACTCCAGCCTGGGCGACGGGAAGACTCTGTCTCAAAAAAAAAAAAAAAAA A G CANX Ensembl:ENSG00000127022 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1394291384 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15407946 RMVar_hsa_circ_358735,RMVar_hsa_circ_328988,RMVar_hsa_circ_309008,RMVar_hsa_circ_282791,RMVar_hsa_circ_277193,RMVar_hsa_circ_236650,RMVar_hsa_circ_236651,RMVar_hsa_circ_236649,RMVar_hsa_circ_358280,RMVar_hsa_circ_373278,RMVar_hsa_circ_74601,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_283752,RMVar_hsa_circ_16635,RMVar_hsa_circ_306623,RMVar_hsa_circ_342219,RMVar_hsa_circ_278860,RMVar_hsa_circ_280622,RMVar_hsa_circ_270449,RMVar_hsa_circ_236662,RMVar_hsa_circ_236664,RMVar_hsa_circ_236665,RMVar_hsa_circ_236666,RMVar_hsa_circ_236663 8819 RMVar_ID_8819 Human_SNP_ID_263614967 A-to-I Human chr5 + 179712823 179712821 179712823 TTGGCCTACTGTGACGTCTGCCTCCCGGGTTCAAGCGATTCTCTTGCCACAGCCTCCTGAGTAGC TTGGCCTACTGTGACGTCTGCCTCCCGGGTT__AGCGATTCTCTTGCCACAGCCTCCTGAGTAGC TCA T CANX Ensembl:ENSG00000127022 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1413788314 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_15407966 RMVar_hsa_circ_358735,RMVar_hsa_circ_328988,RMVar_hsa_circ_309008,RMVar_hsa_circ_282791,RMVar_hsa_circ_277193,RMVar_hsa_circ_236650,RMVar_hsa_circ_236651,RMVar_hsa_circ_236649,RMVar_hsa_circ_358280,RMVar_hsa_circ_373278,RMVar_hsa_circ_74601,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_283752,RMVar_hsa_circ_16635,RMVar_hsa_circ_306623,RMVar_hsa_circ_342219,RMVar_hsa_circ_278860,RMVar_hsa_circ_280622,RMVar_hsa_circ_270449,RMVar_hsa_circ_236662,RMVar_hsa_circ_236664,RMVar_hsa_circ_236665,RMVar_hsa_circ_236666,RMVar_hsa_circ_236663 8820 RMVar_ID_8820 Human_SNP_ID_263615253 A-to-I Human chr5 + 179713841 179713830 179713841 GAGGCTGTGGTATAAAAGGATCCCTTGAGTCCAGGATTCGAGATTGCAGTGAGCTATGATTGGGC GAGGCTGTGGTATAAAAGGATC___________GGATTCGAGATTGCAGTGAGCTATGATTGGGC CCCTTGAGTCCA C CANX Ensembl:ENSG00000127022 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs571306214 Functional Loss DEL dbSNP153 23..33 33 - - - Human_RBP_ID_15407996 RMVar_hsa_circ_358735,RMVar_hsa_circ_328988,RMVar_hsa_circ_309008,RMVar_hsa_circ_282791,RMVar_hsa_circ_277193,RMVar_hsa_circ_236650,RMVar_hsa_circ_236651,RMVar_hsa_circ_236649,RMVar_hsa_circ_358280,RMVar_hsa_circ_373278,RMVar_hsa_circ_74601,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_283752,RMVar_hsa_circ_16635,RMVar_hsa_circ_306623,RMVar_hsa_circ_342219,RMVar_hsa_circ_278860,RMVar_hsa_circ_280622,RMVar_hsa_circ_270449,RMVar_hsa_circ_236662,RMVar_hsa_circ_236664,RMVar_hsa_circ_236665,RMVar_hsa_circ_236666,RMVar_hsa_circ_236663 8821 RMVar_ID_8821 Human_SNP_ID_263615314 A-to-I Human chr5 + 179714068 179714068 179714068 TTGCCCAGGCTGGAGTGCAGTGGCCTGATCTCAGCTCACTGCAACTTCTGCCTCCCGGGTTCAAG TTGCCCAGGCTGGAGTGCAGTGGCCTGATCTCGGCTCACTGCAACTTCTGCCTCCCGGGTTCAAG A G CANX Ensembl:ENSG00000127022 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1207252236 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_358735,RMVar_hsa_circ_328988,RMVar_hsa_circ_309008,RMVar_hsa_circ_282791,RMVar_hsa_circ_277193,RMVar_hsa_circ_236650,RMVar_hsa_circ_236651,RMVar_hsa_circ_236649,RMVar_hsa_circ_358280,RMVar_hsa_circ_373278,RMVar_hsa_circ_74601,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_283752,RMVar_hsa_circ_16635,RMVar_hsa_circ_306623,RMVar_hsa_circ_342219,RMVar_hsa_circ_278860,RMVar_hsa_circ_280622,RMVar_hsa_circ_270449,RMVar_hsa_circ_236662,RMVar_hsa_circ_236664,RMVar_hsa_circ_236665,RMVar_hsa_circ_236666,RMVar_hsa_circ_236663 8822 RMVar_ID_8822 Human_SNP_ID_263615333 A-to-I Human chr5 + 179714138 179714138 179714138 CTCCTGCCTCAGCCTCCTGAATAGTTGGGACTATAGGCATGCGCCACCATGCCCGGCCAATTTTT CTCCTGCCTCAGCCTCCTGAATAGTTGGGACTGTAGGCATGCGCCACCATGCCCGGCCAATTTTT A G CANX Ensembl:ENSG00000127022 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1217394277 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_358735,RMVar_hsa_circ_328988,RMVar_hsa_circ_309008,RMVar_hsa_circ_282791,RMVar_hsa_circ_277193,RMVar_hsa_circ_236650,RMVar_hsa_circ_236651,RMVar_hsa_circ_236649,RMVar_hsa_circ_358280,RMVar_hsa_circ_373278,RMVar_hsa_circ_74601,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_283752,RMVar_hsa_circ_16635,RMVar_hsa_circ_306623,RMVar_hsa_circ_342219,RMVar_hsa_circ_278860,RMVar_hsa_circ_280622,RMVar_hsa_circ_270449,RMVar_hsa_circ_236662,RMVar_hsa_circ_236664,RMVar_hsa_circ_236665,RMVar_hsa_circ_236666,RMVar_hsa_circ_236663 8823 RMVar_ID_8823 Human_SNP_ID_263615729 A-to-I Human chr5 + 179715520 179715520 179715520 AGATCACACCACTGCACTCCAGCCTGGGAGACAAAGCGAGACTCTGTCTCAAAAAAATAAAATAA AGATCACACCACTGCACTCCAGCCTGGGAGACGAAGCGAGACTCTGTCTCAAAAAAATAAAATAA A G CANX Ensembl:ENSG00000127022 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1032465955 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_358735,RMVar_hsa_circ_328988,RMVar_hsa_circ_309008,RMVar_hsa_circ_282791,RMVar_hsa_circ_277193,RMVar_hsa_circ_236650,RMVar_hsa_circ_236651,RMVar_hsa_circ_236649,RMVar_hsa_circ_358280,RMVar_hsa_circ_373278,RMVar_hsa_circ_74601,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_283752,RMVar_hsa_circ_16635,RMVar_hsa_circ_306623,RMVar_hsa_circ_342219,RMVar_hsa_circ_278860,RMVar_hsa_circ_280622,RMVar_hsa_circ_270449,RMVar_hsa_circ_236662,RMVar_hsa_circ_236664,RMVar_hsa_circ_236665,RMVar_hsa_circ_236666,RMVar_hsa_circ_236663 8824 RMVar_ID_8824 Human_SNP_ID_263617453 A-to-I Human chr5 + 179722146 179722146 179722146 GAGGTCAGCCATTCGAGACCAGCCTGGCCAACATAGTGAAACACCATCTCTACTAAAAGCACAAA GAGGTCAGCCATTCGAGACCAGCCTGGCCAACGTAGTGAAACACCATCTCTACTAAAAGCACAAA A G CANX Ensembl:ENSG00000127022 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs985969674 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_358735,RMVar_hsa_circ_328988,RMVar_hsa_circ_309008,RMVar_hsa_circ_236651,RMVar_hsa_circ_97640,RMVar_hsa_circ_359776,RMVar_hsa_circ_236654,RMVar_hsa_circ_97356,RMVar_hsa_circ_236660,RMVar_hsa_circ_306623,RMVar_hsa_circ_342219,RMVar_hsa_circ_278860,RMVar_hsa_circ_236665,RMVar_hsa_circ_236666,RMVar_hsa_circ_236667,RMVar_hsa_circ_35863,RMVar_hsa_circ_358930 8825 RMVar_ID_8825 Human_SNP_ID_263618310 A-to-I Human chr5 + 179725300 179725300 179725300 GTGATCTCGGTTCACTGCAGCCTTTGCCTCCCAGATTCAAGCGATTCTCCCACCTGGGCCTCCCA GTGATCTCGGTTCACTGCAGCCTTTGCCTCCCGGATTCAAGCGATTCTCCCACCTGGGCCTCCCA A G CANX Ensembl:ENSG00000127022 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1398792722 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_309008,RMVar_hsa_circ_97640,RMVar_hsa_circ_236654,RMVar_hsa_circ_97356,RMVar_hsa_circ_236660 8826 RMVar_ID_8826 Human_SNP_ID_263620864 A-to-I Human chr5 + 179734790 179734790 179734790 CTCCTCAGTCCTCCCGCCTCAGCCTCCTGAGTAACTGGGATCAACCACAGCTGCACATCACCATG CTCCTCAGTCCTCCCGCCTCAGCCTCCTGAGTGACTGGGATCAACCACAGCTGCACATCACCATG A G MAML1 Ensembl:ENSG00000161021 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1019546267 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8612346 RMVar_hsa_circ_114909,RMVar_hsa_circ_236671 8827 RMVar_ID_8827 Human_SNP_ID_263622101 A-to-I Human chr5 + 179739586 179739586 179739586 TGCATCTGTATTCTCAGCTCCTCGGGAGACCGAAGTAGGAGGATTGCGTGGGACCGGGAGGTAAA TGCATCTGTATTCTCAGCTCCTCGGGAGACCGGAGTAGGAGGATTGCGTGGGACCGGGAGGTAAA A G MAML1 Ensembl:ENSG00000161021 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1356852291 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114909,RMVar_hsa_circ_236671 8828 RMVar_ID_8828 Human_SNP_ID_263622587 A-to-I Human chr5 + 179741498 179741498 179741498 CTTGAGATCAGGAGTTCAAGGGCAGCCTGGCCAAAATGGTGAAACCCCGTCTCTGGTAAAAAATA CTTGAGATCAGGAGTTCAAGGGCAGCCTGGCCGAAATGGTGAAACCCCGTCTCTGGTAAAAAATA A G MAML1 Ensembl:ENSG00000161021 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170852412 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114909,RMVar_hsa_circ_236671 8829 RMVar_ID_8829 Human_SNP_ID_263623471 A-to-I Human chr5 + 179744717 179744717 179744717 TTTTATTTTTAGTAGAGACGAGGTTTCACCATATTGGCTAAGCTGGTCTTGAACTCCTGGCCTCA TTTTATTTTTAGTAGAGACGAGGTTTCACCATCTTGGCTAAGCTGGTCTTGAACTCCTGGCCTCA A C MAML1 Ensembl:ENSG00000161021 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs925401475 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15408780 RMVar_hsa_circ_114909,RMVar_hsa_circ_236671 8830 RMVar_ID_8830 Human_SNP_ID_263625455 A-to-I Human chr5 + 179751883 179751870 179751883 AAAATTAGCCAGGCTTGGTGGTGTACACCTGTAGTTCCAGCTACTAGGGAGGCTGAGGTGAGAGG AAAATTAGCCAGGCTTGGTG_____________GTTCCAGCTACTAGGGAGGCTGAGGTGAGAGG GGTGTACACCTGTA G MAML1 Ensembl:ENSG00000161021 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1422334603 Functional Loss DEL dbSNP153 21..33 33 - - - RMVar_hsa_circ_114909,RMVar_hsa_circ_236671 8831 RMVar_ID_8831 Human_SNP_ID_263630744 A-to-I Human chr5 + 179769814 179769814 179769814 ACCTCAAGTGATCCACTCATCTCGGCCTCCCAAAGTGCTGAGATTACAGGCGTGAGCCACCACGC ACCTCAAGTGATCCACTCATCTCGGCCTCCCAGAGTGCTGAGATTACAGGCGTGAGCCACCACGC A G MAML1 Ensembl:ENSG00000161021 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1261933661 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114909,RMVar_hsa_circ_236671,RMVar_hsa_circ_319115,RMVar_hsa_circ_236673,RMVar_hsa_circ_307487,RMVar_hsa_circ_236675 8832 RMVar_ID_8832 Human_SNP_ID_263631357 A-to-I Human chr5 + 179772324 179772324 179772324 TATTTTTAGTAGAGATGGGCTTTCACCATGTTAGCCAGGCTGATCTCACATACCTGACCTCGTGA TATTTTTAGTAGAGATGGGCTTTCACCATGTTGGCCAGGCTGATCTCACATACCTGACCTCGTGA A G MAML1 Ensembl:ENSG00000161021 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,cerebellum - 29129909,30559470 RNA-Seq:(High) rs541762219 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15409098 RMVar_hsa_circ_114909,RMVar_hsa_circ_236671 8833 RMVar_ID_8833 Human_SNP_ID_263633614 A-to-I Human chr5 + 179781329 179781329 179781329 TTTGCTTGTAGTCTCAGGTACGCAGGAGACTGAAGAGAGATGATCGCTTGAGGCCAGGAGTTTGG TTTGCTTGTAGTCTCAGGTACGCAGGAGACTGGAGAGAGATGATCGCTTGAGGCCAGGAGTTTGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1305421831 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17575949 8834 RMVar_ID_8834 Human_SNP_ID_263636525 A-to-I Human chr5 - 179791316 179791316 179791316 GAAGTTAGGAGTTTGAGGTCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAA GAAGTTAGGAGTTTGAGGTCAGCCTGGCCAACTTGGTGAAACCCCATCTCTACTAAAAATACAAA T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs960585221 Functional Loss SNV dbSNP153 33..33 33 - - - 8835 RMVar_ID_8835 Human_SNP_ID_263636526 A-to-I Human chr5 - 179791316 179791316 179791316 GAAGTTAGGAGTTTGAGGTCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAA GAAGTTAGGAGTTTGAGGTCAGCCTGGCCAACGTGGTGAAACCCCATCTCTACTAAAAATACAAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs960585221 Functional Loss SNV dbSNP153 33..33 33 - - - 8836 RMVar_ID_8836 Human_SNP_ID_263643482 A-to-I Human chr5 + 179811122 179811122 179811122 GGGAGTGGTGGCGGGCACCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATAGCTTCAA GGGAGTGGTGGCGGGCACCTGTAGTCCCAGCTGCTCGGGAGGCTGAGGCAGGAGAATAGCTTCAA A G SQSTM1 Ensembl:ENSG00000161011 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1487751181 Functional Loss SNV dbSNP153 33..33 33 - - - 8837 RMVar_ID_8837 Human_SNP_ID_263643498 A-to-I Human chr5 + 179811183 179811183 179811183 TCAACCTGTGAGGCGGAGCTTTCAGTGAGCCGAGATCGCACCACTGCACTCCAGCCTGGGCGACA TCAACCTGTGAGGCGGAGCTTTCAGTGAGCCGCGATCGCACCACTGCACTCCAGCCTGGGCGACA A C SQSTM1 Ensembl:ENSG00000161011 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1168891862 Functional Loss SNV dbSNP153 33..33 33 - - - 8838 RMVar_ID_8838 Human_SNP_ID_263644456 A-to-I Human chr5 + 179813645 179813645 179813645 AATAAAAGCCAGGCATGTTGGCATGTACCTGTAGTCCTAGCTGCTCAGGGGGTGAGGCGGGAGGA AATAAAAGCCAGGCATGTTGGCATGTACCTGTTGTCCTAGCTGCTCAGGGGGTGAGGCGGGAGGA A T SQSTM1 Ensembl:ENSG00000161011 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1456460989 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25886111 RMVar_hsa_circ_32329 8839 RMVar_ID_8839 Human_SNP_ID_263648652 A-to-I Human chr5 + 179826762 179826752 179826762 AGCTGGGATTATAGGTGCCCACCACAACGCCTAGCTATTTTTTGTATTTTTAGTAGAGACGGGGT AGCTGGGATTATAGGTGCCCACC__________GCTATTTTTTGTATTTTTAGTAGAGACGGGGT CACAACGCCTA C SQSTM1 Ensembl:ENSG00000161011 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1420071801 Functional Loss DEL dbSNP153 24..33 33 - - - 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_236691 8840 RMVar_ID_8840 Human_SNP_ID_263648661 A-to-I Human chr5 + 179826781 179826781 179826781 CACCACAACGCCTAGCTATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACTGTGTTGGCCAGGC CACCACAACGCCTAGCTATTTTTTGTATTTTTGGTAGAGACGGGGTTTCACTGTGTTGGCCAGGC A G SQSTM1 Ensembl:ENSG00000161011 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1307479161 Functional Loss SNV dbSNP153 33..33 33 - - - 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_236691 8841 RMVar_ID_8841 Human_SNP_ID_263649605 A-to-I Human chr5 + 179829818 179829818 179829818 GAACATAGAATGCAAGATAGTTTCTTGGCACCAGGCATGGTGGCTCATGCCTGTAATCCCAACAC GAACATAGAATGCAAGATAGTTTCTTGGCACCGGGCATGGTGGCTCATGCCTGTAATCCCAACAC A G SQSTM1 Ensembl:ENSG00000161011 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs957221633 Functional Loss SNV dbSNP153 33..33 33 - - - 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_236691 8842 RMVar_ID_8842 Human_SNP_ID_263649682 A-to-I Human chr5 + 179830091 179830090 179830092 GGATTGTACCACTGCACTCCATCCTGGGAGACAGAAACAGACCTTGTCTCAAACAAAACAAAACA GGATTGTACCACTGCACTCCATCCTGGGAGAC__AAACAGACCTTGTCTCAAACAAAACAAAACA CAG C SQSTM1 Ensembl:ENSG00000161011 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1429429755 Functional Loss DEL dbSNP153 33..34 33 - - - 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_236691 8843 RMVar_ID_8843 Human_SNP_ID_263649885 A-to-I Human chr5 + 179830658 179830658 179830658 TCAGCTCACTGCAGTTTCCACCTCCTGGGTTCAAGCAATTTTCTGCCTCAGCCTCCCGAGTAGCT TCAGCTCACTGCAGTTTCCACCTCCTGGGTTCGAGCAATTTTCTGCCTCAGCCTCCCGAGTAGCT A G SQSTM1 Ensembl:ENSG00000161011 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1184322596 Functional Loss SNV dbSNP153 33..33 33 - - - 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_236691 8844 RMVar_ID_8844 Human_SNP_ID_263649889 A-to-I Human chr5 + 179830662 179830662 179830662 CTCACTGCAGTTTCCACCTCCTGGGTTCAAGCAATTTTCTGCCTCAGCCTCCCGAGTAGCTGGGA CTCACTGCAGTTTCCACCTCCTGGGTTCAAGCTATTTTCTGCCTCAGCCTCCCGAGTAGCTGGGA A T SQSTM1 Ensembl:ENSG00000161011 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs186748738 Functional Loss SNV dbSNP153 33..33 33 - - - 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_236691 8845 RMVar_ID_8845 Human_SNP_ID_263649924 A-to-I Human chr5 + 179830799 179830799 179830799 AGGCTGGTCTTGAACTCCTGACCTCATGATCTACCTGCCTTCGTCTCCCAAAGTGCTGGGATTAC AGGCTGGTCTTGAACTCCTGACCTCATGATCTGCCTGCCTTCGTCTCCCAAAGTGCTGGGATTAC A G SQSTM1 Ensembl:ENSG00000161011 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1362526123 Functional Loss SNV dbSNP153 33..33 33 - - - 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_236691 8846 RMVar_ID_8846 Human_SNP_ID_263649938 A-to-I Human chr5 + 179830830 179830830 179830830 TACCTGCCTTCGTCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGTGCCCAGCCCCGTGCC TACCTGCCTTCGTCTCCCAAAGTGCTGGGATTGCAGGCATGAGCCACTGTGCCCAGCCCCGTGCC A G SQSTM1 Ensembl:ENSG00000161011 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042305067 Functional Loss SNV dbSNP153 33..33 33 - - - 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_236691 8847 RMVar_ID_8847 Human_SNP_ID_263649967 A-to-I Human chr5 + 179830912 179830912 179830912 TTTTGTAGAGATGGGGTCTTGCCATGCTGCCCAGGCCGATTTTGAACTCCTGGGCTCAAGAGATT TTTTGTAGAGATGGGGTCTTGCCATGCTGCCCGGGCCGATTTTGAACTCCTGGGCTCAAGAGATT A G SQSTM1 Ensembl:ENSG00000161011 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1416989495 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15409998 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_236691 8848 RMVar_ID_8848 Human_SNP_ID_263649989 A-to-I Human chr5 + 179830963 179830963 179830963 GGGCTCAAGAGATTTCTCATGTTGTTCTCCCAAAGTGTTAGGATTACATGCATGAGTCACTGTGC GGGCTCAAGAGATTTCTCATGTTGTTCTCCCAGAGTGTTAGGATTACATGCATGAGTCACTGTGC A G SQSTM1 Ensembl:ENSG00000161011 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs558718441 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15410001 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_236691 8849 RMVar_ID_8849 Human_SNP_ID_263650117 A-to-I Human chr5 + 179831411 179831411 179831411 AGGCTGGGTGCAGTGGCTCATGCCTGTAATCCAAGCACTTTGGGAGGCCAAGGCAGGCAGATCAC AGGCTGGGTGCAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGCAGATCAC A C SQSTM1 Ensembl:ENSG00000161011 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs146857387 Functional Loss SNV dbSNP153 33..33 33 - - - 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_236691 8850 RMVar_ID_8850 Human_SNP_ID_263650190 A-to-I Human chr5 + 179831577 179831577 179831577 CCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCTGGTGGGCAGAGGCTGCAGTGAGC CCAGCTACTCGGGAGGCTGAGGCAGGAGAATCCCTTGAACCTGGTGGGCAGAGGCTGCAGTGAGC A C SQSTM1 Ensembl:ENSG00000161011 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1331169031 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22727764 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_236691 8851 RMVar_ID_8851 Human_SNP_ID_263650211 A-to-I Human chr5 + 179831643 179831643 179831643 GAGAGATTGCGGCACTGCGCTCCAGCCTGGGCAACAGAGCGAGACTCTGTCTACAAAACAAAGGA GAGAGATTGCGGCACTGCGCTCCAGCCTGGGCGACAGAGCGAGACTCTGTCTACAAAACAAAGGA A G SQSTM1 Ensembl:ENSG00000161011 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1011244496 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15410020 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_236691 8852 RMVar_ID_8852 Human_SNP_ID_263650331 A-to-I Human chr5 + 179831968 179831967 179831969 ACCACGCCCAGCTGATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATATTAGCCAGGGTAG ACCACGCCCAGCTGATTTTTTGTATTTTTAGT__AGACGGGGTTTCACCATATTAGCCAGGGTAG TAG T SQSTM1 Ensembl:ENSG00000161011 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1449544975 Functional Loss DEL dbSNP153 33..34 33 - - - 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_236691 8853 RMVar_ID_8853 Human_SNP_ID_263650724 A-to-I Human chr5 + 179833030 179833030 179833030 CTTCACGGCTTGCTCTTTCCTCCTCCGCCTCTAGGCATTGAAGTTGATATCGATGTGGAGCACGG CTTCACGGCTTGCTCTTTCCTCCTCCGCCTCTGGGCATTGAAGTTGATATCGATGTGGAGCACGG A G SQSTM1 Ensembl:ENSG00000161011 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs111688869 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19126997,Human_RBP_ID_22459075,Human_RBP_ID_22553195,Human_RBP_ID_23313999,Human_RBP_ID_26351900 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 8854 RMVar_ID_8854 Human_SNP_ID_263650725 A-to-I Human chr5 + 179833030 179833030 179833030 CTTCACGGCTTGCTCTTTCCTCCTCCGCCTCTAGGCATTGAAGTTGATATCGATGTGGAGCACGG CTTCACGGCTTGCTCTTTCCTCCTCCGCCTCTTGGCATTGAAGTTGATATCGATGTGGAGCACGG A T SQSTM1 Ensembl:ENSG00000161011 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs111688869 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19126997,Human_RBP_ID_22459075,Human_RBP_ID_22553195,Human_RBP_ID_23313999,Human_RBP_ID_26351900 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 8855 RMVar_ID_8855 Human_SNP_ID_263653418 A-to-I Human chr5 - 179838559 179838547 179838560 TGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGAGATTACAGGCGCGTGCCACCACGCCAGGTTAA TGATTCTCCTGCCTCAGCCTCCCGAGTAGCT_____________CGTGCCACCACGCCAGGTTAA GCGCCTGTAATCTC G MRNIP Ensembl:ENSG00000161010 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1442857721 Functional Loss DEL dbSNP153 32..44 33 - - - 8856 RMVar_ID_8856 Human_SNP_ID_263653501 A-to-I Human chr5 - 179838775 179838775 179838775 GGGGTTTCACCATGTTGCCCAAACTGGTGTCAAACTCCTGGGCTCAAGCAATCTGCCTGCCTCAG GGGGTTTCACCATGTTGCCCAAACTGGTGTCAGACTCCTGGGCTCAAGCAATCTGCCTGCCTCAG T C MRNIP Ensembl:ENSG00000161010 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1382965554 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3767085,Human_RBP_ID_15566269 8857 RMVar_ID_8857 Human_SNP_ID_263653910 A-to-I Human chr5 - 179840235 179840235 179840235 GGCTAATCTTTAAAAAATATTTTGTAGAGGCCAGGCGCAGTGGCTCACACCTGTAATCTCAGCAC GGCTAATCTTTAAAAAATATTTTGTAGAGGCCGGGCGCAGTGGCTCACACCTGTAATCTCAGCAC T C MRNIP Ensembl:ENSG00000161010 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1368878077 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15410236 8858 RMVar_ID_8858 Human_SNP_ID_263653957 A-to-I Human chr5 - 179840404 179840402 179840404 GTGTTGTCTTGTTCTTTTTTGTTTTCTGAGACAGGGTCTCACTCTGTCTACCCAGGCTGGAGTGC GTGTTGTCTTGTTCTTTTTTGTTTTCTGAGAC__GGTCTCACTCTGTCTACCCAGGCTGGAGTGC CCT C MRNIP Ensembl:ENSG00000161010 Protein coding intron GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459,32596459 RNA-Seq:(High) rs1476006904 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_3767087,Human_RBP_ID_15410241,Human_RBP_ID_24505958 8859 RMVar_ID_8859 Human_SNP_ID_263655624 A-to-I Human chr5 + 179844686 179844686 179844686 GGGCTCAAGTGATCTACCCACCTCGGCCTCCCAAAGTGCTGGGATTACAAGCGTGAAGTACGCAT GGGCTCAAGTGATCTACCCACCTCGGCCTCCCGAAGTGCTGGGATTACAAGCGTGAAGTACGCAT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1368064159 Functional Loss SNV dbSNP153 33..33 33 - - - 8860 RMVar_ID_8860 Human_SNP_ID_263667140 A-to-I Human chr5 - 179882082 179882082 179882082 AAATTAGCCGGGCATGGTGGCACACACCTGTAATCCCAGCTACTTGGGAACCTGAGGCAGGAGAA AAATTAGCCGGGCATGGTGGCACACACCTGTAGTCCCAGCTACTTGGGAACCTGAGGCAGGAGAA T C TBC1D9B Ensembl:ENSG00000197226 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1389615263 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_236702,RMVar_hsa_circ_121729,RMVar_hsa_circ_94254,RMVar_hsa_circ_236703 8861 RMVar_ID_8861 Human_SNP_ID_263676176 A-to-I Human chr5 - 179915323 179915323 179915323 TTTTTGTTTGTTTGTTTGTTTTATTTCGAGACAGGGTGTCACTCTGTCGCCCAGACTGGAGTGCA TTTTTGTTTGTTTGTTTGTTTTATTTCGAGACGGGGTGTCACTCTGTCGCCCAGACTGGAGTGCA T C RNF130 Ensembl:ENSG00000113269 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1336008692 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7502445 8862 RMVar_ID_8862 Human_SNP_ID_333839879 A-to-I Human chr7 - 105002027 105002027 105002027 TAGAAACCGTATCTCACTCTGTGGCCCAGGCTAGAGTTCAGTGGCAGGGCAGTCATAGCTCATTG TAGAAACCGTATCTCACTCTGTGGCCCAGGCTGGAGTTCAGTGGCAGGGCAGTCATAGCTCATTG T C LINC01004 Ensembl:ENSG00000228393 lincRNA intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1166407624 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7669896,Human_RBP_ID_15959028 8863 RMVar_ID_8863 Human_SNP_ID_333840292 A-to-I Human chr7 - 105003543 105003543 105003543 GCACAGTGGCTCATGACTAATCCTAGCACTTTAGGAGGCAGAGGTGGGTGGATCCCTTGAGTCTA GCACAGTGGCTCATGACTAATCCTAGCACTTTGGGAGGCAGAGGTGGGTGGATCCCTTGAGTCTA T C LINC01004 Ensembl:ENSG00000228393 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1175245879 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7669931,Human_RBP_ID_26132967 8864 RMVar_ID_8864 Human_SNP_ID_333840781 A-to-I Human chr7 - 105005294 105005294 105005294 AAAACTGACCTTGGCCGGGCACGGTGGCTCACACCTGTAATCCCAGCACTTTGAGAGGCTGAGGC AAAACTGACCTTGGCCGGGCACGGTGGCTCACTCCTGTAATCCCAGCACTTTGAGAGGCTGAGGC T A LINC01004 Ensembl:ENSG00000228393 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs182601443 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21952950 8865 RMVar_ID_8865 Human_SNP_ID_333841020 A-to-I Human chr7 - 105006114 105006114 105006114 TCACACCATTCTGCTGCTTCAGCCTCCCGAGTAGCTCGGACTACAGGCGCCTGCCACCATGCCCG TCACACCATTCTGCTGCTTCAGCCTCCCGAGTCGCTCGGACTACAGGCGCCTGCCACCATGCCCG T G LINC01004 Ensembl:ENSG00000228393 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1350791217 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8273618,Human_RBP_ID_15959213 8866 RMVar_ID_8866 Human_SNP_ID_333841043 A-to-I Human chr7 - 105006169 105006169 105006169 CAGGCTGGAGTGCAGTGGTGCAATCTCAGCTCACTGCACACTCTGCCTCCTGGGTTCACACCATT CAGGCTGGAGTGCAGTGGTGCAATCTCAGCTCTCTGCACACTCTGCCTCCTGGGTTCACACCATT T A LINC01004 Ensembl:ENSG00000228393 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs912267950 Functional Loss SNV dbSNP153 33..33 33 - - - 8867 RMVar_ID_8867 Human_SNP_ID_333841417 A-to-I Human chr7 - 105007486 105007486 105007486 GTGGGAGGATCACCACTTGAGGCCAAGAGATCAAGATCAGCCTGGGCAACATAGCAAGACCCCCA GTGGGAGGATCACCACTTGAGGCCAAGAGATCGAGATCAGCCTGGGCAACATAGCAAGACCCCCA T C LINC01004 Ensembl:ENSG00000228393 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs988176939 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3867930,Human_RBP_ID_5251348,Human_RBP_ID_10318564,Human_RBP_ID_15959278,Human_RBP_ID_26054873 8868 RMVar_ID_8868 Human_SNP_ID_333841464 A-to-I Human chr7 - 105007655 105007655 105007655 AATTGCAAGTAGCCTGTAATCCCAGCACTTTTAGGAGTCCGAGGCAGGAGGATCACTTGAGACCA AATTGCAAGTAGCCTGTAATCCCAGCACTTTTGGGAGTCCGAGGCAGGAGGATCACTTGAGACCA T C LINC01004 Ensembl:ENSG00000228393 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1279041037 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7669982,Human_RBP_ID_15959292 8869 RMVar_ID_8869 Human_SNP_ID_333841532 A-to-I Human chr7 - 105007826 105007826 105007826 TAATTAGCTGGGCGTAGTGGTGCACATCTGTAATCCAGCTACTCAGGAGGCTGAGGCATGAGAAT TAATTAGCTGGGCGTAGTGGTGCACATCTGTACTCCAGCTACTCAGGAGGCTGAGGCATGAGAAT T G LINC01004 Ensembl:ENSG00000228393 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1321967925 Functional Loss SNV dbSNP153 33..33 33 - - - 8870 RMVar_ID_8870 Human_SNP_ID_333841555 A-to-I Human chr7 - 105007966 105007966 105007966 CTGGCTGATTATAGGCATGGTGGCTTATGCCTATAATCCCAGCACTTTGGGAGGCCAGGGTTGGT CTGGCTGATTATAGGCATGGTGGCTTATGCCTGTAATCCCAGCACTTTGGGAGGCCAGGGTTGGT T C LINC01004 Ensembl:ENSG00000228393 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs917204460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5251241 8871 RMVar_ID_8871 Human_SNP_ID_333842660 A-to-I Human chr7 - 105011923 105011923 105011923 CTGGTCTCGAACTCTCGAGATCCGCCCGTCTCAGCTTCCCAAAGTGCTGGGATTATAGGCATGAG CTGGTCTCGAACTCTCGAGATCCGCCCGTCTCGGCTTCCCAAAGTGCTGGGATTATAGGCATGAG T C LINC01004 Ensembl:ENSG00000228393 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs575303676 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3867936,Human_RBP_ID_16272269,Human_RBP_ID_26054932 8872 RMVar_ID_8872 Human_SNP_ID_333842671 A-to-I Human chr7 - 105011970 105011970 105011970 ATTTTTTCTATTTTTAGTAGAGACGGGGTTTCACCCCATTGACCAGGCTGGTCTCGAACTCTCGA ATTTTTTCTATTTTTAGTAGAGACGGGGTTTCGCCCCATTGACCAGGCTGGTCTCGAACTCTCGA T C LINC01004 Ensembl:ENSG00000228393 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs558312951 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3867936,Human_RBP_ID_15959500 8873 RMVar_ID_8873 Human_SNP_ID_333842672 A-to-I Human chr7 - 105011970 105011970 105011970 ATTTTTTCTATTTTTAGTAGAGACGGGGTTTCACCCCATTGACCAGGCTGGTCTCGAACTCTCGA ATTTTTTCTATTTTTAGTAGAGACGGGGTTTCCCCCCATTGACCAGGCTGGTCTCGAACTCTCGA T G LINC01004 Ensembl:ENSG00000228393 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs558312951 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3867936,Human_RBP_ID_15959500 8874 RMVar_ID_8874 Human_SNP_ID_333842695 A-to-I Human chr7 - 105012039 105012039 105012039 TCAGGCGAGTCTCCTGCCTCAGCCTCCCAGGTAGCTGGGATTACAGGCGCCCACAACCACACCCT TCAGGCGAGTCTCCTGCCTCAGCCTCCCAGGTGGCTGGGATTACAGGCGCCCACAACCACACCCT T C LINC01004 Ensembl:ENSG00000228393 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1187072144 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26054938 8875 RMVar_ID_8875 Human_SNP_ID_333847349 A-to-I Human chr7 + 105028238 105028238 105028238 TCGCCCAGGCTGGAGTGCAGTGGTGTGATCTCAGCTCACTGCAACCTCCGCCTCCTGTGTTCAAG TCGCCCAGGCTGGAGTGCAGTGGTGTGATCTCTGCTCACTGCAACCTCCGCCTCCTGTGTTCAAG A T KMT2E Ensembl:ENSG00000005483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1408011964 Functional Loss SNV dbSNP153 33..33 33 - - - 8876 RMVar_ID_8876 Human_SNP_ID_333847365 A-to-I Human chr7 + 105028314 105028314 105028314 CCTCAGGCTCCCGAGTAGGTGGGACCACAGGCATGGGCCACCATGCCCGACTAATCTTTGAATTT CCTCAGGCTCCCGAGTAGGTGGGACCACAGGCGTGGGCCACCATGCCCGACTAATCTTTGAATTT A G KMT2E Ensembl:ENSG00000005483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs890192460 Functional Loss SNV dbSNP153 33..33 33 - - - 8877 RMVar_ID_8877 Human_SNP_ID_333847472 A-to-I Human chr7 + 105028713 105028713 105028713 TTTTGTAGAGATGGGATTTCACCATGTTGTCCAGGGTGGTCTCTAATTCTTGAGCTCAAGTGATC TTTTGTAGAGATGGGATTTCACCATGTTGTCCTGGGTGGTCTCTAATTCTTGAGCTCAAGTGATC A T KMT2E Ensembl:ENSG00000005483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1481218687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17577543,Human_RBP_ID_23196362 8878 RMVar_ID_8878 Human_SNP_ID_333847594 A-to-I Human chr7 + 105029195 105029194 105029196 TGAGTCAGAGGAATTGCTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCTGAGATCGTGCCACTGC TGAGTCAGAGGAATTGCTTGAACCTGGGAGGC__AGGTTGCAGTGAGCTGAGATCGTGCCACTGC CAG C KMT2E Ensembl:ENSG00000005483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs765243366 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_26055033 8879 RMVar_ID_8879 Human_SNP_ID_333848265 A-to-I Human chr7 + 105031631 105031631 105031631 AAAATTAGCTGGGCATGGTGGCGGGCACCTGTAATGCCACCTAATTGGGAGGCTGAGGCAGGAGA AAAATTAGCTGGGCATGGTGGCGGGCACCTGTGATGCCACCTAATTGGGAGGCTGAGGCAGGAGA A G KMT2E Ensembl:ENSG00000005483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs887758193 Functional Loss SNV dbSNP153 33..33 33 - - - 8880 RMVar_ID_8880 Human_SNP_ID_333848820 A-to-I Human chr7 + 105033598 105033598 105033598 TCGGCCCACTGCAAGCTCCACCTCCTGGGTTCATGCCATTCTTCGGCCTCAGCCTCCTGCGTAGC TCGGCCCACTGCAAGCTCCACCTCCTGGGTTCCTGCCATTCTTCGGCCTCAGCCTCCTGCGTAGC A C KMT2E Ensembl:ENSG00000005483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1057368570 Functional Loss SNV dbSNP153 33..33 33 - - - 8881 RMVar_ID_8881 Human_SNP_ID_333848863 A-to-I Human chr7 + 105033706 105033706 105033706 TATTTTTAGTAAAGATGGGGTTTCGCTGTGTTAGCCAGGGTGGTCTCGATCTCCTGACCTCGTGA TATTTTTAGTAAAGATGGGGTTTCGCTGTGTTGGCCAGGGTGGTCTCGATCTCCTGACCTCGTGA A G KMT2E Ensembl:ENSG00000005483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1038920809 Functional Loss SNV dbSNP153 33..33 33 - - - 8882 RMVar_ID_8882 Human_SNP_ID_333849044 A-to-I Human chr7 + 105034326 105034326 105034326 ATGATCACAGCTTGCTGTAATCTCAAACTCCTAGGCTCAGACGATCCTCCTACCTCAATCTCCTG ATGATCACAGCTTGCTGTAATCTCAAACTCCTGGGCTCAGACGATCCTCCTACCTCAATCTCCTG A G KMT2E Ensembl:ENSG00000005483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs571936863 Functional Loss SNV dbSNP153 33..33 33 - - - 8883 RMVar_ID_8883 Human_SNP_ID_333849051 A-to-I Human chr7 + 105034345 105034345 105034345 ATCTCAAACTCCTAGGCTCAGACGATCCTCCTACCTCAATCTCCTGAATAGTTAGGACTACAGGC ATCTCAAACTCCTAGGCTCAGACGATCCTCCTGCCTCAATCTCCTGAATAGTTAGGACTACAGGC A G KMT2E Ensembl:ENSG00000005483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1338796684 Functional Loss SNV dbSNP153 33..33 33 - - - 8884 RMVar_ID_8884 Human_SNP_ID_333849058 A-to-I Human chr7 + 105034372 105034372 105034372 CTCCTACCTCAATCTCCTGAATAGTTAGGACTACAGGCTTGCACCACCATGCCCAGCTAATTTTT CTCCTACCTCAATCTCCTGAATAGTTAGGACTGCAGGCTTGCACCACCATGCCCAGCTAATTTTT A G KMT2E Ensembl:ENSG00000005483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1257728642 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15960051 8885 RMVar_ID_8885 Human_SNP_ID_333850978 A-to-I Human chr7 + 105041601 105041601 105041601 TTTTGTGTTTTTAGTAGAGATGGGGTTTCATCATTTTGGCTAGGCTGGTCTCGAACTCCTGACCT TTTTGTGTTTTTAGTAGAGATGGGGTTTCATCGTTTTGGCTAGGCTGGTCTCGAACTCCTGACCT A G KMT2E Ensembl:ENSG00000005483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs990382540 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6704,RMVar_hsa_circ_118314,RMVar_hsa_circ_278570,RMVar_hsa_circ_370704,RMVar_hsa_circ_320297,RMVar_hsa_circ_312768,RMVar_hsa_circ_264827,RMVar_hsa_circ_118535,RMVar_hsa_circ_85463,RMVar_hsa_circ_62855,RMVar_hsa_circ_247513,RMVar_hsa_circ_247517,RMVar_hsa_circ_247519,RMVar_hsa_circ_247521,RMVar_hsa_circ_247520,RMVar_hsa_circ_247518,RMVar_hsa_circ_247515,RMVar_hsa_circ_247516,RMVar_hsa_circ_247514,RMVar_hsa_circ_247525,RMVar_hsa_circ_268874,RMVar_hsa_circ_297368,RMVar_hsa_circ_328971,RMVar_hsa_circ_343320,RMVar_hsa_circ_315721,RMVar_hsa_circ_60526,RMVar_hsa_circ_75002,RMVar_hsa_circ_247526,RMVar_hsa_circ_247527 8886 RMVar_ID_8886 Human_SNP_ID_333851120 A-to-I Human chr7 + 105042101 105042101 105042101 CTCACTGCAACCTCCAGGCTCAAGGGATTCTCATGTCTTAGCCTCCTGAGTAGCTGGGATTACAG CTCACTGCAACCTCCAGGCTCAAGGGATTCTCGTGTCTTAGCCTCCTGAGTAGCTGGGATTACAG A G KMT2E Ensembl:ENSG00000005483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1391463100 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6704,RMVar_hsa_circ_118314,RMVar_hsa_circ_278570,RMVar_hsa_circ_370704,RMVar_hsa_circ_320297,RMVar_hsa_circ_312768,RMVar_hsa_circ_264827,RMVar_hsa_circ_118535,RMVar_hsa_circ_85463,RMVar_hsa_circ_62855,RMVar_hsa_circ_247513,RMVar_hsa_circ_247517,RMVar_hsa_circ_247519,RMVar_hsa_circ_247521,RMVar_hsa_circ_247520,RMVar_hsa_circ_247518,RMVar_hsa_circ_247515,RMVar_hsa_circ_247516,RMVar_hsa_circ_247514,RMVar_hsa_circ_247525,RMVar_hsa_circ_268874,RMVar_hsa_circ_297368,RMVar_hsa_circ_328971,RMVar_hsa_circ_343320,RMVar_hsa_circ_315721,RMVar_hsa_circ_60526,RMVar_hsa_circ_75002,RMVar_hsa_circ_247526,RMVar_hsa_circ_247527 8887 RMVar_ID_8887 Human_SNP_ID_333852939 A-to-I Human chr7 + 105049183 105049183 105049183 GAAATAAGTGCTGGCCAGGCGTGGTGGCTCACACCTGTATTCCTAGCACTTTGGGAGGCTGAGGC GAAATAAGTGCTGGCCAGGCGTGGTGGCTCACGCCTGTATTCCTAGCACTTTGGGAGGCTGAGGC A G KMT2E Ensembl:ENSG00000005483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1300376362 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6704,RMVar_hsa_circ_118314,RMVar_hsa_circ_278570,RMVar_hsa_circ_370704,RMVar_hsa_circ_320297,RMVar_hsa_circ_312768,RMVar_hsa_circ_264827,RMVar_hsa_circ_118535,RMVar_hsa_circ_85463,RMVar_hsa_circ_62855,RMVar_hsa_circ_247513,RMVar_hsa_circ_247517,RMVar_hsa_circ_247519,RMVar_hsa_circ_247520,RMVar_hsa_circ_247518,RMVar_hsa_circ_247515,RMVar_hsa_circ_247516,RMVar_hsa_circ_247514,RMVar_hsa_circ_247525,RMVar_hsa_circ_268874,RMVar_hsa_circ_297368,RMVar_hsa_circ_328971,RMVar_hsa_circ_343320,RMVar_hsa_circ_315721,RMVar_hsa_circ_60526,RMVar_hsa_circ_75002,RMVar_hsa_circ_247526,RMVar_hsa_circ_247527 8888 RMVar_ID_8888 Human_SNP_ID_333852955 A-to-I Human chr7 + 105049238 105049238 105049238 AGGCTGAGGCTGGCCAGTTGCTTGAGCCCAAGAATTCAAGACTGGCCTTGGCAACATGATGAAAC AGGCTGAGGCTGGCCAGTTGCTTGAGCCCAAGGATTCAAGACTGGCCTTGGCAACATGATGAAAC A G KMT2E Ensembl:ENSG00000005483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388392693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15960387 RMVar_hsa_circ_6704,RMVar_hsa_circ_118314,RMVar_hsa_circ_278570,RMVar_hsa_circ_370704,RMVar_hsa_circ_320297,RMVar_hsa_circ_312768,RMVar_hsa_circ_264827,RMVar_hsa_circ_118535,RMVar_hsa_circ_85463,RMVar_hsa_circ_62855,RMVar_hsa_circ_247513,RMVar_hsa_circ_247517,RMVar_hsa_circ_247519,RMVar_hsa_circ_247520,RMVar_hsa_circ_247518,RMVar_hsa_circ_247515,RMVar_hsa_circ_247516,RMVar_hsa_circ_247514,RMVar_hsa_circ_247525,RMVar_hsa_circ_268874,RMVar_hsa_circ_297368,RMVar_hsa_circ_328971,RMVar_hsa_circ_343320,RMVar_hsa_circ_315721,RMVar_hsa_circ_60526,RMVar_hsa_circ_75002,RMVar_hsa_circ_247526,RMVar_hsa_circ_247527 8889 RMVar_ID_8889 Human_SNP_ID_333854317 A-to-I Human chr7 + 105053742 105053742 105053742 TACAAAAATTTTTTTAAAAATTAGCCAGGCATAGTGGCTCATGACTGTAATCTACTCAGGAGGCT TACAAAAATTTTTTTAAAAATTAGCCAGGCATGGTGGCTCATGACTGTAATCTACTCAGGAGGCT A G KMT2E Ensembl:ENSG00000005483 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs541458816 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6704,RMVar_hsa_circ_118314,RMVar_hsa_circ_278570,RMVar_hsa_circ_370704,RMVar_hsa_circ_320297,RMVar_hsa_circ_312768,RMVar_hsa_circ_264827,RMVar_hsa_circ_118535,RMVar_hsa_circ_85463,RMVar_hsa_circ_62855,RMVar_hsa_circ_247513,RMVar_hsa_circ_247517,RMVar_hsa_circ_247519,RMVar_hsa_circ_247520,RMVar_hsa_circ_247518,RMVar_hsa_circ_247515,RMVar_hsa_circ_247516,RMVar_hsa_circ_247514,RMVar_hsa_circ_247525,RMVar_hsa_circ_268874,RMVar_hsa_circ_297368,RMVar_hsa_circ_328971,RMVar_hsa_circ_343320,RMVar_hsa_circ_315721,RMVar_hsa_circ_60526,RMVar_hsa_circ_75002,RMVar_hsa_circ_247526,RMVar_hsa_circ_247527 8890 RMVar_ID_8890 Human_SNP_ID_333854393 A-to-I Human chr7 + 105054034 105054028 105054035 GTCTCTACTAAAAATAAAAAAACTTACCGGGCATGGTGGCACGTGCCTGTAATCCCGGCTACTAC GTCTCTACTAAAAATAAAAAAACTTAC_______GGTGGCACGTGCCTGTAATCCCGGCTACTAC CCGGGCAT C KMT2E Ensembl:ENSG00000005483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1562894399 Functional Loss DEL dbSNP153 28..34 33 - - - Human_RBP_ID_7670386 RMVar_hsa_circ_6704,RMVar_hsa_circ_118314,RMVar_hsa_circ_278570,RMVar_hsa_circ_370704,RMVar_hsa_circ_320297,RMVar_hsa_circ_312768,RMVar_hsa_circ_264827,RMVar_hsa_circ_118535,RMVar_hsa_circ_85463,RMVar_hsa_circ_62855,RMVar_hsa_circ_247513,RMVar_hsa_circ_247517,RMVar_hsa_circ_247519,RMVar_hsa_circ_247520,RMVar_hsa_circ_247518,RMVar_hsa_circ_247515,RMVar_hsa_circ_247516,RMVar_hsa_circ_247514,RMVar_hsa_circ_247525,RMVar_hsa_circ_268874,RMVar_hsa_circ_297368,RMVar_hsa_circ_328971,RMVar_hsa_circ_343320,RMVar_hsa_circ_315721,RMVar_hsa_circ_60526,RMVar_hsa_circ_75002,RMVar_hsa_circ_247526,RMVar_hsa_circ_247527 8891 RMVar_ID_8891 Human_SNP_ID_333854416 A-to-I Human chr7 + 105054087 105054087 105054087 CCCGGCTACTACGAGGCTGAGACACGAGAATCACTTGAACCCGGGAGGTGGAGCTTGTAGTGAGC CCCGGCTACTACGAGGCTGAGACACGAGAATCGCTTGAACCCGGGAGGTGGAGCTTGTAGTGAGC A G KMT2E Ensembl:ENSG00000005483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1050305194 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15960478 RMVar_hsa_circ_6704,RMVar_hsa_circ_118314,RMVar_hsa_circ_278570,RMVar_hsa_circ_370704,RMVar_hsa_circ_320297,RMVar_hsa_circ_312768,RMVar_hsa_circ_264827,RMVar_hsa_circ_118535,RMVar_hsa_circ_85463,RMVar_hsa_circ_62855,RMVar_hsa_circ_247513,RMVar_hsa_circ_247517,RMVar_hsa_circ_247519,RMVar_hsa_circ_247520,RMVar_hsa_circ_247518,RMVar_hsa_circ_247515,RMVar_hsa_circ_247516,RMVar_hsa_circ_247514,RMVar_hsa_circ_247525,RMVar_hsa_circ_268874,RMVar_hsa_circ_297368,RMVar_hsa_circ_328971,RMVar_hsa_circ_343320,RMVar_hsa_circ_315721,RMVar_hsa_circ_60526,RMVar_hsa_circ_75002,RMVar_hsa_circ_247526,RMVar_hsa_circ_247527 8892 RMVar_ID_8892 Human_SNP_ID_333858132 A-to-I Human chr7 + 105067742 105067742 105067742 CCTGTAATCCCAGCACTTTGGGAGGCCGAGGTAGGTAGATCATGAGAGCCCAGGAGTTCGAGACC CCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGTAGATCATGAGAGCCCAGGAGTTCGAGACC A G KMT2E Ensembl:ENSG00000005483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1370715093 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15960842,Human_RBP_ID_26055318 RMVar_hsa_circ_6704,RMVar_hsa_circ_118314,RMVar_hsa_circ_320297,RMVar_hsa_circ_312768,RMVar_hsa_circ_264827,RMVar_hsa_circ_118535,RMVar_hsa_circ_85463,RMVar_hsa_circ_62855,RMVar_hsa_circ_247513,RMVar_hsa_circ_247517,RMVar_hsa_circ_247518,RMVar_hsa_circ_247515,RMVar_hsa_circ_247516,RMVar_hsa_circ_247514,RMVar_hsa_circ_247525,RMVar_hsa_circ_268874,RMVar_hsa_circ_297368,RMVar_hsa_circ_328971,RMVar_hsa_circ_60526,RMVar_hsa_circ_75002,RMVar_hsa_circ_247526,RMVar_hsa_circ_305843,RMVar_hsa_circ_336300,RMVar_hsa_circ_375891,RMVar_hsa_circ_307264,RMVar_hsa_circ_300394,RMVar_hsa_circ_97438,RMVar_hsa_circ_269953,RMVar_hsa_circ_247529,RMVar_hsa_circ_247531,RMVar_hsa_circ_247533,RMVar_hsa_circ_24970,RMVar_hsa_circ_247532,RMVar_hsa_circ_247530,RMVar_hsa_circ_247528,RMVar_hsa_circ_265602,RMVar_hsa_circ_30416,RMVar_hsa_circ_9488,RMVar_hsa_circ_58296,RMVar_hsa_circ_291841,RMVar_hsa_circ_311411,RMVar_hsa_circ_95948,RMVar_hsa_circ_25725,RMVar_hsa_circ_247539,RMVar_hsa_circ_247540,RMVar_hsa_circ_247538 8893 RMVar_ID_8893 Human_SNP_ID_333858327 A-to-I Human chr7 + 105068472 105068472 105068472 TTTATTGGAACAAACTTCTCTTTTTTTTTTTTAAGACAGGATCTCACATTGTCGAACAGGCTACG TTTATTGGAACAAACTTCTCTTTTTTTTTTTTGAGACAGGATCTCACATTGTCGAACAGGCTACG A G KMT2E Ensembl:ENSG00000005483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1000406142 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_82326,Human_RBP_ID_7670492,Human_RBP_ID_15960861 Human_Splice_Rec_906943 RMVar_hsa_circ_6704,RMVar_hsa_circ_118314,RMVar_hsa_circ_320297,RMVar_hsa_circ_312768,RMVar_hsa_circ_264827,RMVar_hsa_circ_118535,RMVar_hsa_circ_85463,RMVar_hsa_circ_62855,RMVar_hsa_circ_247513,RMVar_hsa_circ_247517,RMVar_hsa_circ_247518,RMVar_hsa_circ_247515,RMVar_hsa_circ_247516,RMVar_hsa_circ_247514,RMVar_hsa_circ_247525,RMVar_hsa_circ_268874,RMVar_hsa_circ_297368,RMVar_hsa_circ_328971,RMVar_hsa_circ_60526,RMVar_hsa_circ_75002,RMVar_hsa_circ_247526,RMVar_hsa_circ_305843,RMVar_hsa_circ_336300,RMVar_hsa_circ_375891,RMVar_hsa_circ_307264,RMVar_hsa_circ_300394,RMVar_hsa_circ_97438,RMVar_hsa_circ_269953,RMVar_hsa_circ_247529,RMVar_hsa_circ_247531,RMVar_hsa_circ_247533,RMVar_hsa_circ_24970,RMVar_hsa_circ_247532,RMVar_hsa_circ_247530,RMVar_hsa_circ_247528,RMVar_hsa_circ_265602,RMVar_hsa_circ_30416,RMVar_hsa_circ_9488,RMVar_hsa_circ_58296,RMVar_hsa_circ_291841,RMVar_hsa_circ_311411,RMVar_hsa_circ_95948,RMVar_hsa_circ_25725,RMVar_hsa_circ_247539,RMVar_hsa_circ_247540,RMVar_hsa_circ_247538 8894 RMVar_ID_8894 Human_SNP_ID_333858358 A-to-I Human chr7 + 105068578 105068578 105068578 GTGATTCTCCCATCCTTCCACCTCAGCTTGCCAAGTAGCTGGGACTACAGGCATCGCCACCATGC GTGATTCTCCCATCCTTCCACCTCAGCTTGCCGAGTAGCTGGGACTACAGGCATCGCCACCATGC A G KMT2E Ensembl:ENSG00000005483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs921731988 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6704,RMVar_hsa_circ_118314,RMVar_hsa_circ_320297,RMVar_hsa_circ_312768,RMVar_hsa_circ_264827,RMVar_hsa_circ_118535,RMVar_hsa_circ_85463,RMVar_hsa_circ_62855,RMVar_hsa_circ_247513,RMVar_hsa_circ_247517,RMVar_hsa_circ_247515,RMVar_hsa_circ_247516,RMVar_hsa_circ_247514,RMVar_hsa_circ_247525,RMVar_hsa_circ_268874,RMVar_hsa_circ_297368,RMVar_hsa_circ_328971,RMVar_hsa_circ_60526,RMVar_hsa_circ_75002,RMVar_hsa_circ_247526,RMVar_hsa_circ_305843,RMVar_hsa_circ_336300,RMVar_hsa_circ_375891,RMVar_hsa_circ_307264,RMVar_hsa_circ_300394,RMVar_hsa_circ_97438,RMVar_hsa_circ_269953,RMVar_hsa_circ_247529,RMVar_hsa_circ_247531,RMVar_hsa_circ_247533,RMVar_hsa_circ_24970,RMVar_hsa_circ_247532,RMVar_hsa_circ_247530,RMVar_hsa_circ_247528,RMVar_hsa_circ_265602,RMVar_hsa_circ_30416,RMVar_hsa_circ_9488,RMVar_hsa_circ_58296,RMVar_hsa_circ_291841,RMVar_hsa_circ_311411,RMVar_hsa_circ_95948,RMVar_hsa_circ_25725,RMVar_hsa_circ_247539,RMVar_hsa_circ_247540,RMVar_hsa_circ_247538,RMVar_hsa_circ_247541 8895 RMVar_ID_8895 Human_SNP_ID_333858359 A-to-I Human chr7 + 105068582 105068582 105068582 TTCTCCCATCCTTCCACCTCAGCTTGCCAAGTAGCTGGGACTACAGGCATCGCCACCATGCCTGA TTCTCCCATCCTTCCACCTCAGCTTGCCAAGTGGCTGGGACTACAGGCATCGCCACCATGCCTGA A G KMT2E Ensembl:ENSG00000005483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs562491808 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6704,RMVar_hsa_circ_118314,RMVar_hsa_circ_320297,RMVar_hsa_circ_312768,RMVar_hsa_circ_264827,RMVar_hsa_circ_118535,RMVar_hsa_circ_85463,RMVar_hsa_circ_62855,RMVar_hsa_circ_247513,RMVar_hsa_circ_247517,RMVar_hsa_circ_247515,RMVar_hsa_circ_247516,RMVar_hsa_circ_247514,RMVar_hsa_circ_247525,RMVar_hsa_circ_268874,RMVar_hsa_circ_297368,RMVar_hsa_circ_328971,RMVar_hsa_circ_60526,RMVar_hsa_circ_75002,RMVar_hsa_circ_247526,RMVar_hsa_circ_305843,RMVar_hsa_circ_336300,RMVar_hsa_circ_375891,RMVar_hsa_circ_307264,RMVar_hsa_circ_300394,RMVar_hsa_circ_97438,RMVar_hsa_circ_269953,RMVar_hsa_circ_247529,RMVar_hsa_circ_247531,RMVar_hsa_circ_247533,RMVar_hsa_circ_24970,RMVar_hsa_circ_247532,RMVar_hsa_circ_247530,RMVar_hsa_circ_247528,RMVar_hsa_circ_265602,RMVar_hsa_circ_30416,RMVar_hsa_circ_9488,RMVar_hsa_circ_58296,RMVar_hsa_circ_291841,RMVar_hsa_circ_311411,RMVar_hsa_circ_95948,RMVar_hsa_circ_25725,RMVar_hsa_circ_247539,RMVar_hsa_circ_247540,RMVar_hsa_circ_247538,RMVar_hsa_circ_247541 8896 RMVar_ID_8896 Human_SNP_ID_333858829 A-to-I Human chr7 + 105070369 105070369 105070369 TTAAGAATTGTTGGTTGGGCGCAGTGGCTCACAGCTATAATCCTAGCACTTTTGGAGGCTGAGGC TTAAGAATTGTTGGTTGGGCGCAGTGGCTCACGGCTATAATCCTAGCACTTTTGGAGGCTGAGGC A G KMT2E Ensembl:ENSG00000005483 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs938093089 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6704,RMVar_hsa_circ_118314,RMVar_hsa_circ_320297,RMVar_hsa_circ_312768,RMVar_hsa_circ_264827,RMVar_hsa_circ_118535,RMVar_hsa_circ_85463,RMVar_hsa_circ_62855,RMVar_hsa_circ_247513,RMVar_hsa_circ_247517,RMVar_hsa_circ_247515,RMVar_hsa_circ_247516,RMVar_hsa_circ_247514,RMVar_hsa_circ_247525,RMVar_hsa_circ_268874,RMVar_hsa_circ_297368,RMVar_hsa_circ_328971,RMVar_hsa_circ_60526,RMVar_hsa_circ_75002,RMVar_hsa_circ_247526,RMVar_hsa_circ_305843,RMVar_hsa_circ_336300,RMVar_hsa_circ_375891,RMVar_hsa_circ_307264,RMVar_hsa_circ_300394,RMVar_hsa_circ_97438,RMVar_hsa_circ_269953,RMVar_hsa_circ_247529,RMVar_hsa_circ_247531,RMVar_hsa_circ_247533,RMVar_hsa_circ_24970,RMVar_hsa_circ_247532,RMVar_hsa_circ_247530,RMVar_hsa_circ_247528,RMVar_hsa_circ_265602,RMVar_hsa_circ_30416,RMVar_hsa_circ_9488,RMVar_hsa_circ_58296,RMVar_hsa_circ_291841,RMVar_hsa_circ_311411,RMVar_hsa_circ_95948,RMVar_hsa_circ_25725,RMVar_hsa_circ_247539,RMVar_hsa_circ_247540,RMVar_hsa_circ_247538,RMVar_hsa_circ_247541 8897 RMVar_ID_8897 Human_SNP_ID_333858830 A-to-I Human chr7 + 105070373 105070373 105070373 GAATTGTTGGTTGGGCGCAGTGGCTCACAGCTATAATCCTAGCACTTTTGGAGGCTGAGGCGGGT GAATTGTTGGTTGGGCGCAGTGGCTCACAGCTGTAATCCTAGCACTTTTGGAGGCTGAGGCGGGT A G KMT2E Ensembl:ENSG00000005483 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs796951596 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6704,RMVar_hsa_circ_118314,RMVar_hsa_circ_320297,RMVar_hsa_circ_312768,RMVar_hsa_circ_264827,RMVar_hsa_circ_118535,RMVar_hsa_circ_85463,RMVar_hsa_circ_62855,RMVar_hsa_circ_247513,RMVar_hsa_circ_247517,RMVar_hsa_circ_247515,RMVar_hsa_circ_247516,RMVar_hsa_circ_247514,RMVar_hsa_circ_247525,RMVar_hsa_circ_268874,RMVar_hsa_circ_297368,RMVar_hsa_circ_328971,RMVar_hsa_circ_60526,RMVar_hsa_circ_75002,RMVar_hsa_circ_247526,RMVar_hsa_circ_305843,RMVar_hsa_circ_336300,RMVar_hsa_circ_375891,RMVar_hsa_circ_307264,RMVar_hsa_circ_300394,RMVar_hsa_circ_97438,RMVar_hsa_circ_269953,RMVar_hsa_circ_247529,RMVar_hsa_circ_247531,RMVar_hsa_circ_247533,RMVar_hsa_circ_24970,RMVar_hsa_circ_247532,RMVar_hsa_circ_247530,RMVar_hsa_circ_247528,RMVar_hsa_circ_265602,RMVar_hsa_circ_30416,RMVar_hsa_circ_9488,RMVar_hsa_circ_58296,RMVar_hsa_circ_291841,RMVar_hsa_circ_311411,RMVar_hsa_circ_95948,RMVar_hsa_circ_25725,RMVar_hsa_circ_247539,RMVar_hsa_circ_247540,RMVar_hsa_circ_247538,RMVar_hsa_circ_247541 8898 RMVar_ID_8898 Human_SNP_ID_333859496 A-to-I Human chr7 + 105072050 105072050 105072050 TTACCATTAGGAGGCCGGGCGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGGGAGGCCCAG TTACCATTAGGAGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGGGAGGCCCAG A G KMT2E Ensembl:ENSG00000005483 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1449514565 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6704,RMVar_hsa_circ_118314,RMVar_hsa_circ_320297,RMVar_hsa_circ_312768,RMVar_hsa_circ_264827,RMVar_hsa_circ_118535,RMVar_hsa_circ_85463,RMVar_hsa_circ_62855,RMVar_hsa_circ_247513,RMVar_hsa_circ_247517,RMVar_hsa_circ_247515,RMVar_hsa_circ_247516,RMVar_hsa_circ_247514,RMVar_hsa_circ_247525,RMVar_hsa_circ_268874,RMVar_hsa_circ_297368,RMVar_hsa_circ_328971,RMVar_hsa_circ_60526,RMVar_hsa_circ_75002,RMVar_hsa_circ_247526,RMVar_hsa_circ_305843,RMVar_hsa_circ_336300,RMVar_hsa_circ_375891,RMVar_hsa_circ_307264,RMVar_hsa_circ_300394,RMVar_hsa_circ_97438,RMVar_hsa_circ_269953,RMVar_hsa_circ_247529,RMVar_hsa_circ_247531,RMVar_hsa_circ_247533,RMVar_hsa_circ_24970,RMVar_hsa_circ_247532,RMVar_hsa_circ_247530,RMVar_hsa_circ_247528,RMVar_hsa_circ_265602,RMVar_hsa_circ_30416,RMVar_hsa_circ_9488,RMVar_hsa_circ_58296,RMVar_hsa_circ_291841,RMVar_hsa_circ_311411,RMVar_hsa_circ_95948,RMVar_hsa_circ_25725,RMVar_hsa_circ_247539,RMVar_hsa_circ_247540,RMVar_hsa_circ_247538,RMVar_hsa_circ_247541 8899 RMVar_ID_8899 Human_SNP_ID_333859682 A-to-I Human chr7 + 105072658 105072658 105072658 GTATTTCACTTAACTGTTAAATGCTCATGCCTATAATCCCAGCACTTTGGGAGGCCGAGGTGGGC GTATTTCACTTAACTGTTAAATGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGC A G KMT2E Ensembl:ENSG00000005483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs555413371 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15960953,Human_RBP_ID_26055360 RMVar_hsa_circ_6704,RMVar_hsa_circ_118314,RMVar_hsa_circ_320297,RMVar_hsa_circ_312768,RMVar_hsa_circ_264827,RMVar_hsa_circ_118535,RMVar_hsa_circ_85463,RMVar_hsa_circ_62855,RMVar_hsa_circ_247513,RMVar_hsa_circ_247517,RMVar_hsa_circ_247515,RMVar_hsa_circ_247516,RMVar_hsa_circ_247514,RMVar_hsa_circ_247525,RMVar_hsa_circ_268874,RMVar_hsa_circ_297368,RMVar_hsa_circ_328971,RMVar_hsa_circ_60526,RMVar_hsa_circ_75002,RMVar_hsa_circ_247526,RMVar_hsa_circ_305843,RMVar_hsa_circ_336300,RMVar_hsa_circ_375891,RMVar_hsa_circ_307264,RMVar_hsa_circ_300394,RMVar_hsa_circ_97438,RMVar_hsa_circ_269953,RMVar_hsa_circ_247529,RMVar_hsa_circ_247531,RMVar_hsa_circ_247533,RMVar_hsa_circ_24970,RMVar_hsa_circ_247532,RMVar_hsa_circ_247530,RMVar_hsa_circ_247528,RMVar_hsa_circ_265602,RMVar_hsa_circ_30416,RMVar_hsa_circ_9488,RMVar_hsa_circ_58296,RMVar_hsa_circ_291841,RMVar_hsa_circ_311411,RMVar_hsa_circ_95948,RMVar_hsa_circ_25725,RMVar_hsa_circ_247539,RMVar_hsa_circ_247540,RMVar_hsa_circ_247538,RMVar_hsa_circ_247541 8900 RMVar_ID_8900 Human_SNP_ID_333859735 A-to-I Human chr7 + 105072863 105072862 105072864 TTGAACCCAGGAGGCAGAGGTTGCAGTGAGCCAAGATTGCGCCATTGCACTCCAGCCTGGGCAAT TTGAACCCAGGAGGCAGAGGTTGCAGTGAGCC__GATTGCGCCATTGCACTCCAGCCTGGGCAAT CAA C KMT2E Ensembl:ENSG00000005483 Protein coding intron GSE38233;GSE107867 cultured B-cells;ASD brains,Fragile X samples from NIH NeuroBioBank - 24183664,30559470 RNA-Seq:(High) rs1461961185 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_6704,RMVar_hsa_circ_118314,RMVar_hsa_circ_320297,RMVar_hsa_circ_312768,RMVar_hsa_circ_264827,RMVar_hsa_circ_118535,RMVar_hsa_circ_85463,RMVar_hsa_circ_62855,RMVar_hsa_circ_247513,RMVar_hsa_circ_247517,RMVar_hsa_circ_247515,RMVar_hsa_circ_247516,RMVar_hsa_circ_247514,RMVar_hsa_circ_247525,RMVar_hsa_circ_268874,RMVar_hsa_circ_297368,RMVar_hsa_circ_328971,RMVar_hsa_circ_60526,RMVar_hsa_circ_75002,RMVar_hsa_circ_247526,RMVar_hsa_circ_305843,RMVar_hsa_circ_336300,RMVar_hsa_circ_375891,RMVar_hsa_circ_307264,RMVar_hsa_circ_300394,RMVar_hsa_circ_97438,RMVar_hsa_circ_269953,RMVar_hsa_circ_247529,RMVar_hsa_circ_247531,RMVar_hsa_circ_247533,RMVar_hsa_circ_24970,RMVar_hsa_circ_247532,RMVar_hsa_circ_247530,RMVar_hsa_circ_247528,RMVar_hsa_circ_265602,RMVar_hsa_circ_30416,RMVar_hsa_circ_9488,RMVar_hsa_circ_58296,RMVar_hsa_circ_291841,RMVar_hsa_circ_311411,RMVar_hsa_circ_95948,RMVar_hsa_circ_25725,RMVar_hsa_circ_247539,RMVar_hsa_circ_247540,RMVar_hsa_circ_247538,RMVar_hsa_circ_247541 8901 RMVar_ID_8901 Human_SNP_ID_333859736 A-to-I Human chr7 + 105072863 105072863 105072863 TTGAACCCAGGAGGCAGAGGTTGCAGTGAGCCAAGATTGCGCCATTGCACTCCAGCCTGGGCAAT TTGAACCCAGGAGGCAGAGGTTGCAGTGAGCCGAGATTGCGCCATTGCACTCCAGCCTGGGCAAT A G KMT2E Ensembl:ENSG00000005483 Protein coding intron GSE38233;GSE107867 cultured B-cells;ASD brains,Fragile X samples from NIH NeuroBioBank - 24183664,30559470 RNA-Seq:(High) rs534531083 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6704,RMVar_hsa_circ_118314,RMVar_hsa_circ_320297,RMVar_hsa_circ_312768,RMVar_hsa_circ_264827,RMVar_hsa_circ_118535,RMVar_hsa_circ_85463,RMVar_hsa_circ_62855,RMVar_hsa_circ_247513,RMVar_hsa_circ_247517,RMVar_hsa_circ_247515,RMVar_hsa_circ_247516,RMVar_hsa_circ_247514,RMVar_hsa_circ_247525,RMVar_hsa_circ_268874,RMVar_hsa_circ_297368,RMVar_hsa_circ_328971,RMVar_hsa_circ_60526,RMVar_hsa_circ_75002,RMVar_hsa_circ_247526,RMVar_hsa_circ_305843,RMVar_hsa_circ_336300,RMVar_hsa_circ_375891,RMVar_hsa_circ_307264,RMVar_hsa_circ_300394,RMVar_hsa_circ_97438,RMVar_hsa_circ_269953,RMVar_hsa_circ_247529,RMVar_hsa_circ_247531,RMVar_hsa_circ_247533,RMVar_hsa_circ_24970,RMVar_hsa_circ_247532,RMVar_hsa_circ_247530,RMVar_hsa_circ_247528,RMVar_hsa_circ_265602,RMVar_hsa_circ_30416,RMVar_hsa_circ_9488,RMVar_hsa_circ_58296,RMVar_hsa_circ_291841,RMVar_hsa_circ_311411,RMVar_hsa_circ_95948,RMVar_hsa_circ_25725,RMVar_hsa_circ_247539,RMVar_hsa_circ_247540,RMVar_hsa_circ_247538,RMVar_hsa_circ_247541 8902 RMVar_ID_8902 Human_SNP_ID_333861762 A-to-I Human chr7 + 105080115 105080115 105080115 GCAATCCTCCTGCCTCGGCCTCCCTAAATGCTAGGATTACAGGCATGAGCCACCAGGTCCAGCCT GCAATCCTCCTGCCTCGGCCTCCCTAAATGCTCGGATTACAGGCATGAGCCACCAGGTCCAGCCT A C KMT2E Ensembl:ENSG00000005483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1214062248 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118314,RMVar_hsa_circ_320297,RMVar_hsa_circ_312768,RMVar_hsa_circ_85463,RMVar_hsa_circ_247513,RMVar_hsa_circ_247515,RMVar_hsa_circ_247516,RMVar_hsa_circ_247514,RMVar_hsa_circ_247525,RMVar_hsa_circ_268874,RMVar_hsa_circ_297368,RMVar_hsa_circ_328971,RMVar_hsa_circ_75002,RMVar_hsa_circ_247526,RMVar_hsa_circ_305843,RMVar_hsa_circ_307264,RMVar_hsa_circ_97438,RMVar_hsa_circ_269953,RMVar_hsa_circ_247529,RMVar_hsa_circ_247531,RMVar_hsa_circ_24970,RMVar_hsa_circ_247530,RMVar_hsa_circ_247528,RMVar_hsa_circ_265602,RMVar_hsa_circ_58296,RMVar_hsa_circ_291841,RMVar_hsa_circ_311411,RMVar_hsa_circ_95948,RMVar_hsa_circ_283141,RMVar_hsa_circ_247539,RMVar_hsa_circ_247540,RMVar_hsa_circ_247538,RMVar_hsa_circ_329791,RMVar_hsa_circ_326863,RMVar_hsa_circ_282476,RMVar_hsa_circ_44389,RMVar_hsa_circ_247544,RMVar_hsa_circ_247545,RMVar_hsa_circ_247542,RMVar_hsa_circ_247543,RMVar_hsa_circ_31369,RMVar_hsa_circ_309561,RMVar_hsa_circ_45149,RMVar_hsa_circ_277243,RMVar_hsa_circ_247549,RMVar_hsa_circ_247550 8903 RMVar_ID_8903 Human_SNP_ID_333863834 A-to-I Human chr7 + 105087585 105087585 105087585 AGCTGGGACTGCAGGCGCACACTGCCACGCCTAGCTAATTTTTTGTGTTTTAGTAGAGACGGGGT AGCTGGGACTGCAGGCGCACACTGCCACGCCTGGCTAATTTTTTGTGTTTTAGTAGAGACGGGGT A G KMT2E Ensembl:ENSG00000005483 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs868387215 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118314,RMVar_hsa_circ_320297,RMVar_hsa_circ_85463,RMVar_hsa_circ_247513,RMVar_hsa_circ_247515,RMVar_hsa_circ_247514,RMVar_hsa_circ_268874,RMVar_hsa_circ_297368,RMVar_hsa_circ_75002,RMVar_hsa_circ_247526,RMVar_hsa_circ_305843,RMVar_hsa_circ_307264,RMVar_hsa_circ_97438,RMVar_hsa_circ_247529,RMVar_hsa_circ_24970,RMVar_hsa_circ_247530,RMVar_hsa_circ_247528,RMVar_hsa_circ_265602,RMVar_hsa_circ_58296,RMVar_hsa_circ_291841,RMVar_hsa_circ_95948,RMVar_hsa_circ_283141,RMVar_hsa_circ_247539,RMVar_hsa_circ_247540,RMVar_hsa_circ_329791,RMVar_hsa_circ_326863,RMVar_hsa_circ_44389,RMVar_hsa_circ_247544,RMVar_hsa_circ_247542,RMVar_hsa_circ_247543,RMVar_hsa_circ_31369,RMVar_hsa_circ_277243,RMVar_hsa_circ_247550 8904 RMVar_ID_8904 Human_SNP_ID_333863838 A-to-I Human chr7 + 105087604 105087604 105087604 CACTGCCACGCCTAGCTAATTTTTTGTGTTTTAGTAGAGACGGGGTTTCACCGTGTTGCCCAGGC CACTGCCACGCCTAGCTAATTTTTTGTGTTTTTGTAGAGACGGGGTTTCACCGTGTTGCCCAGGC A T KMT2E Ensembl:ENSG00000005483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs961563341 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118314,RMVar_hsa_circ_320297,RMVar_hsa_circ_85463,RMVar_hsa_circ_247513,RMVar_hsa_circ_247515,RMVar_hsa_circ_247514,RMVar_hsa_circ_268874,RMVar_hsa_circ_297368,RMVar_hsa_circ_75002,RMVar_hsa_circ_247526,RMVar_hsa_circ_305843,RMVar_hsa_circ_307264,RMVar_hsa_circ_97438,RMVar_hsa_circ_247529,RMVar_hsa_circ_24970,RMVar_hsa_circ_247530,RMVar_hsa_circ_247528,RMVar_hsa_circ_265602,RMVar_hsa_circ_58296,RMVar_hsa_circ_291841,RMVar_hsa_circ_95948,RMVar_hsa_circ_283141,RMVar_hsa_circ_247539,RMVar_hsa_circ_247540,RMVar_hsa_circ_329791,RMVar_hsa_circ_326863,RMVar_hsa_circ_44389,RMVar_hsa_circ_247544,RMVar_hsa_circ_247542,RMVar_hsa_circ_247543,RMVar_hsa_circ_31369,RMVar_hsa_circ_277243,RMVar_hsa_circ_247550 8905 RMVar_ID_8905 Human_SNP_ID_333863839 A-to-I Human chr7 + 105087607 105087607 105087607 TGCCACGCCTAGCTAATTTTTTGTGTTTTAGTAGAGACGGGGTTTCACCGTGTTGCCCAGGCTGG TGCCACGCCTAGCTAATTTTTTGTGTTTTAGTGGAGACGGGGTTTCACCGTGTTGCCCAGGCTGG A G KMT2E Ensembl:ENSG00000005483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs994358381 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118314,RMVar_hsa_circ_320297,RMVar_hsa_circ_85463,RMVar_hsa_circ_247513,RMVar_hsa_circ_247515,RMVar_hsa_circ_247514,RMVar_hsa_circ_268874,RMVar_hsa_circ_297368,RMVar_hsa_circ_75002,RMVar_hsa_circ_247526,RMVar_hsa_circ_305843,RMVar_hsa_circ_307264,RMVar_hsa_circ_97438,RMVar_hsa_circ_247529,RMVar_hsa_circ_24970,RMVar_hsa_circ_247530,RMVar_hsa_circ_247528,RMVar_hsa_circ_265602,RMVar_hsa_circ_58296,RMVar_hsa_circ_291841,RMVar_hsa_circ_95948,RMVar_hsa_circ_283141,RMVar_hsa_circ_247539,RMVar_hsa_circ_247540,RMVar_hsa_circ_329791,RMVar_hsa_circ_326863,RMVar_hsa_circ_44389,RMVar_hsa_circ_247544,RMVar_hsa_circ_247542,RMVar_hsa_circ_247543,RMVar_hsa_circ_31369,RMVar_hsa_circ_277243,RMVar_hsa_circ_247550 8906 RMVar_ID_8906 Human_SNP_ID_333867791 A-to-I Human chr7 + 105102924 105102924 105102924 TTGTAGGCATGCTGCTAAACCATGACATGTACATTTAGTAAAATTCTAGTATGAACCCAGGATTA TTGTAGGCATGCTGCTAAACCATGACATGTACGTTTAGTAAAATTCTAGTATGAACCCAGGATTA A G KMT2E Ensembl:ENSG00000005483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6966377 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118314,RMVar_hsa_circ_85463,RMVar_hsa_circ_247513,RMVar_hsa_circ_247514,RMVar_hsa_circ_268874,RMVar_hsa_circ_97438,RMVar_hsa_circ_247528,RMVar_hsa_circ_265602,RMVar_hsa_circ_58296,RMVar_hsa_circ_95948,RMVar_hsa_circ_247540,RMVar_hsa_circ_326863,RMVar_hsa_circ_247542,RMVar_hsa_circ_72306,RMVar_hsa_circ_71096 8907 RMVar_ID_8907 Human_SNP_ID_333867792 A-to-I Human chr7 + 105102924 105102924 105102924 TTGTAGGCATGCTGCTAAACCATGACATGTACATTTAGTAAAATTCTAGTATGAACCCAGGATTA TTGTAGGCATGCTGCTAAACCATGACATGTACTTTTAGTAAAATTCTAGTATGAACCCAGGATTA A T KMT2E Ensembl:ENSG00000005483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6966377 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118314,RMVar_hsa_circ_85463,RMVar_hsa_circ_247513,RMVar_hsa_circ_247514,RMVar_hsa_circ_268874,RMVar_hsa_circ_97438,RMVar_hsa_circ_247528,RMVar_hsa_circ_265602,RMVar_hsa_circ_58296,RMVar_hsa_circ_95948,RMVar_hsa_circ_247540,RMVar_hsa_circ_326863,RMVar_hsa_circ_247542,RMVar_hsa_circ_72306,RMVar_hsa_circ_71096 8908 RMVar_ID_8908 Human_SNP_ID_333868119 A-to-I Human chr7 + 105103902 105103902 105103902 CACGCTGGAGTGCAGTGGTGTGATCTCGGCTCACTGCAAGCTCCGCCTCCCGGGTTCAAGTGCTT CACGCTGGAGTGCAGTGGTGTGATCTCGGCTCGCTGCAAGCTCCGCCTCCCGGGTTCAAGTGCTT A G KMT2E Ensembl:ENSG00000005483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs533954104 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118314,RMVar_hsa_circ_85463,RMVar_hsa_circ_247513,RMVar_hsa_circ_247514,RMVar_hsa_circ_268874,RMVar_hsa_circ_97438,RMVar_hsa_circ_247528,RMVar_hsa_circ_265602,RMVar_hsa_circ_58296,RMVar_hsa_circ_95948,RMVar_hsa_circ_247540,RMVar_hsa_circ_326863,RMVar_hsa_circ_247542,RMVar_hsa_circ_72306,RMVar_hsa_circ_71096 8909 RMVar_ID_8909 Human_SNP_ID_333868121 A-to-I Human chr7 + 105103907 105103907 105103907 TGGAGTGCAGTGGTGTGATCTCGGCTCACTGCAAGCTCCGCCTCCCGGGTTCAAGTGCTTCTCCT TGGAGTGCAGTGGTGTGATCTCGGCTCACTGCGAGCTCCGCCTCCCGGGTTCAAGTGCTTCTCCT A G KMT2E Ensembl:ENSG00000005483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs902744888 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118314,RMVar_hsa_circ_85463,RMVar_hsa_circ_247513,RMVar_hsa_circ_247514,RMVar_hsa_circ_268874,RMVar_hsa_circ_97438,RMVar_hsa_circ_247528,RMVar_hsa_circ_265602,RMVar_hsa_circ_58296,RMVar_hsa_circ_95948,RMVar_hsa_circ_247540,RMVar_hsa_circ_326863,RMVar_hsa_circ_247542,RMVar_hsa_circ_72306,RMVar_hsa_circ_71096 8910 RMVar_ID_8910 Human_SNP_ID_333868291 A-to-I Human chr7 + 105104566 105104566 105104566 AAAACAAAAAAATTAGCTGGGCATGGTGGTGCACACCTGTAGTCCCAGCTAGTTGGGAGGCTAAG AAAACAAAAAAATTAGCTGGGCATGGTGGTGCCCACCTGTAGTCCCAGCTAGTTGGGAGGCTAAG A C KMT2E Ensembl:ENSG00000005483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1189609980 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118314,RMVar_hsa_circ_85463,RMVar_hsa_circ_247513,RMVar_hsa_circ_247514,RMVar_hsa_circ_268874,RMVar_hsa_circ_97438,RMVar_hsa_circ_247528,RMVar_hsa_circ_265602,RMVar_hsa_circ_58296,RMVar_hsa_circ_95948,RMVar_hsa_circ_247540,RMVar_hsa_circ_326863,RMVar_hsa_circ_247542,RMVar_hsa_circ_72306,RMVar_hsa_circ_71096 8911 RMVar_ID_8911 Human_SNP_ID_333868399 A-to-I Human chr7 + 105104913 105104913 105104913 AAGCTTGGCTGGGCACGGTGGCTCACACCTGTAAACTCAGCACTTTGCAAGGCTGAGGCGGGAGG AAGCTTGGCTGGGCACGGTGGCTCACACCTGTGAACTCAGCACTTTGCAAGGCTGAGGCGGGAGG A G KMT2E Ensembl:ENSG00000005483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1453336330 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118314,RMVar_hsa_circ_85463,RMVar_hsa_circ_247513,RMVar_hsa_circ_247514,RMVar_hsa_circ_268874,RMVar_hsa_circ_97438,RMVar_hsa_circ_247528,RMVar_hsa_circ_265602,RMVar_hsa_circ_58296,RMVar_hsa_circ_95948,RMVar_hsa_circ_247540,RMVar_hsa_circ_326863,RMVar_hsa_circ_247542,RMVar_hsa_circ_72306,RMVar_hsa_circ_71096 8912 RMVar_ID_8912 Human_SNP_ID_333874617 A-to-I Human chr7 - 105125821 105125821 105125821 AACTGCTGGGGAAAGTCCCTCGAAAATACGCTATGTTGGGGAAATACTCCAAGGAGTTTTTCACC AACTGCTGGGGAAAGTCCCTCGAAAATACGCTGTGTTGGGGAAATACTCCAAGGAGTTTTTCACC T C SRPK2 Ensembl:ENSG00000135250 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs757511381 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26055597 Human_Splice_Rec_907046,Human_Splice_Rec_907047,Human_Splice_Rec_907132,Human_Splice_Rec_907133,Human_Splice_Rec_907174,Human_Splice_Rec_907175 RMVar_hsa_circ_28438,RMVar_hsa_circ_91004,RMVar_hsa_circ_99536,RMVar_hsa_circ_124459,RMVar_hsa_circ_247556,RMVar_hsa_circ_247558,RMVar_hsa_circ_80610,RMVar_hsa_circ_247557,RMVar_hsa_circ_247555,RMVar_hsa_circ_28469,RMVar_hsa_circ_3129,RMVar_hsa_circ_55653,RMVar_hsa_circ_65667 8913 RMVar_ID_8913 Human_SNP_ID_333879182 A-to-I Human chr7 - 105144213 105144213 105144213 AAAATTAGCCGGGTGTGATGGTGTGCACCTGTAGTCCTAGCTACATGGGAGGCTGAGGCATGAGA AAAATTAGCCGGGTGTGATGGTGTGCACCTGTGGTCCTAGCTACATGGGAGGCTGAGGCATGAGA T C SRPK2 Ensembl:ENSG00000135250 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1380608494 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91004,RMVar_hsa_circ_99536,RMVar_hsa_circ_124459,RMVar_hsa_circ_247556,RMVar_hsa_circ_247558,RMVar_hsa_circ_80610,RMVar_hsa_circ_247557,RMVar_hsa_circ_247555,RMVar_hsa_circ_65667,RMVar_hsa_circ_16806,RMVar_hsa_circ_70356,RMVar_hsa_circ_82275,RMVar_hsa_circ_284513,RMVar_hsa_circ_65345,RMVar_hsa_circ_73401,RMVar_hsa_circ_371459,RMVar_hsa_circ_247559,RMVar_hsa_circ_247560,RMVar_hsa_circ_64945,RMVar_hsa_circ_372036,RMVar_hsa_circ_292461,RMVar_hsa_circ_247564,RMVar_hsa_circ_21089,RMVar_hsa_circ_37207,RMVar_hsa_circ_247565,RMVar_hsa_circ_247566,RMVar_hsa_circ_247563 8914 RMVar_ID_8914 Human_SNP_ID_333879237 A-to-I Human chr7 - 105144378 105144378 105144378 AAACTAGCTGAGTGTGCTGGTGGACGTCTGTAATCCCGGCTACTCAGGAGGCTAAGGCAGTAGAA AAACTAGCTGAGTGTGCTGGTGGACGTCTGTAGTCCCGGCTACTCAGGAGGCTAAGGCAGTAGAA T C SRPK2 Ensembl:ENSG00000135250 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1002352031 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91004,RMVar_hsa_circ_99536,RMVar_hsa_circ_124459,RMVar_hsa_circ_247556,RMVar_hsa_circ_247558,RMVar_hsa_circ_80610,RMVar_hsa_circ_247557,RMVar_hsa_circ_247555,RMVar_hsa_circ_65667,RMVar_hsa_circ_16806,RMVar_hsa_circ_70356,RMVar_hsa_circ_82275,RMVar_hsa_circ_284513,RMVar_hsa_circ_65345,RMVar_hsa_circ_73401,RMVar_hsa_circ_371459,RMVar_hsa_circ_247559,RMVar_hsa_circ_247560,RMVar_hsa_circ_64945,RMVar_hsa_circ_372036,RMVar_hsa_circ_292461,RMVar_hsa_circ_247564,RMVar_hsa_circ_21089,RMVar_hsa_circ_37207,RMVar_hsa_circ_247565,RMVar_hsa_circ_247566,RMVar_hsa_circ_247563 8915 RMVar_ID_8915 Human_SNP_ID_333879371 A-to-I Human chr7 - 105144958 105144958 105144958 GGGATTACAGGCACCTGCCACCGCACCCAACTAATTTTTGTATTTTTAGTAGAGAGGGGTTTCAC GGGATTACAGGCACCTGCCACCGCACCCAACTGATTTTTGTATTTTTAGTAGAGAGGGGTTTCAC T C SRPK2 Ensembl:ENSG00000135250 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs920918067 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91004,RMVar_hsa_circ_99536,RMVar_hsa_circ_124459,RMVar_hsa_circ_247556,RMVar_hsa_circ_247558,RMVar_hsa_circ_80610,RMVar_hsa_circ_247557,RMVar_hsa_circ_247555,RMVar_hsa_circ_65667,RMVar_hsa_circ_16806,RMVar_hsa_circ_70356,RMVar_hsa_circ_82275,RMVar_hsa_circ_284513,RMVar_hsa_circ_65345,RMVar_hsa_circ_73401,RMVar_hsa_circ_371459,RMVar_hsa_circ_247559,RMVar_hsa_circ_247560,RMVar_hsa_circ_64945,RMVar_hsa_circ_372036,RMVar_hsa_circ_292461,RMVar_hsa_circ_247564,RMVar_hsa_circ_21089,RMVar_hsa_circ_37207,RMVar_hsa_circ_247565,RMVar_hsa_circ_247566,RMVar_hsa_circ_247563 8916 RMVar_ID_8916 Human_SNP_ID_333879389 A-to-I Human chr7 - 105145023 105145023 105145023 CGGCTCACTGCAACCTCCCCCTCCCTGGTTCAAACGATTCTTGTGCCTCAGCCTCCCGAGTAGCT CGGCTCACTGCAACCTCCCCCTCCCTGGTTCAGACGATTCTTGTGCCTCAGCCTCCCGAGTAGCT T C SRPK2 Ensembl:ENSG00000135250 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1221500870 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91004,RMVar_hsa_circ_99536,RMVar_hsa_circ_124459,RMVar_hsa_circ_247556,RMVar_hsa_circ_247558,RMVar_hsa_circ_80610,RMVar_hsa_circ_247557,RMVar_hsa_circ_247555,RMVar_hsa_circ_65667,RMVar_hsa_circ_16806,RMVar_hsa_circ_70356,RMVar_hsa_circ_82275,RMVar_hsa_circ_284513,RMVar_hsa_circ_65345,RMVar_hsa_circ_73401,RMVar_hsa_circ_371459,RMVar_hsa_circ_247559,RMVar_hsa_circ_247560,RMVar_hsa_circ_64945,RMVar_hsa_circ_372036,RMVar_hsa_circ_292461,RMVar_hsa_circ_247564,RMVar_hsa_circ_21089,RMVar_hsa_circ_37207,RMVar_hsa_circ_247565,RMVar_hsa_circ_247566,RMVar_hsa_circ_247563 8917 RMVar_ID_8917 Human_SNP_ID_333881623 A-to-I Human chr7 - 105152791 105152791 105152791 GACCTTGTGATCCGCCCATTTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGTCACCGCGCC GACCTTGTGATCCGCCCATTTCGGCCTCCCAACGTGCTGGGATTACAGGCGTGAGTCACCGCGCC T G SRPK2 Ensembl:ENSG00000135250 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1428347429 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13841,RMVar_hsa_circ_91004,RMVar_hsa_circ_124459,RMVar_hsa_circ_247556,RMVar_hsa_circ_247558,RMVar_hsa_circ_80610,RMVar_hsa_circ_247557,RMVar_hsa_circ_65667,RMVar_hsa_circ_16806,RMVar_hsa_circ_70356,RMVar_hsa_circ_82275,RMVar_hsa_circ_65345,RMVar_hsa_circ_73401,RMVar_hsa_circ_371459,RMVar_hsa_circ_247559,RMVar_hsa_circ_64945,RMVar_hsa_circ_372036,RMVar_hsa_circ_247564,RMVar_hsa_circ_21089,RMVar_hsa_circ_37207,RMVar_hsa_circ_247565,RMVar_hsa_circ_247566,RMVar_hsa_circ_20613,RMVar_hsa_circ_247568 8918 RMVar_ID_8918 Human_SNP_ID_333906415 A-to-I Human chr7 - 105244768 105244768 105244768 AAGCCACATGCCTCCGGGATCATGTCCCGCACAAACTTGGTGTGTTTGGTCAGACGCCCGCGGCG AAGCCACATGCCTCCGGGATCATGTCCCGCACGAACTTGGTGTGTTTGGTCAGACGCCCGCGGCG T C SRPK2 Ensembl:ENSG00000135250 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878958505 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91004,RMVar_hsa_circ_247558,RMVar_hsa_circ_82275,RMVar_hsa_circ_65345,RMVar_hsa_circ_247559,RMVar_hsa_circ_21089,RMVar_hsa_circ_351916,RMVar_hsa_circ_332831,RMVar_hsa_circ_323192,RMVar_hsa_circ_330225,RMVar_hsa_circ_247573 8919 RMVar_ID_8919 Human_SNP_ID_333909609 A-to-I Human chr7 - 105255905 105255905 105255905 TTTTTTTTTTCAATTTGAGATGGACTCACACTATCGCCCAGGCTGGAGTGCAATCTTGACTCATT TTTTTTTTTTCAATTTGAGATGGACTCACACTGTCGCCCAGGCTGGAGTGCAATCTTGACTCATT T C SRPK2 Ensembl:ENSG00000135250 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs535535171 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15962652 RMVar_hsa_circ_91004,RMVar_hsa_circ_247558,RMVar_hsa_circ_82275,RMVar_hsa_circ_65345,RMVar_hsa_circ_247559,RMVar_hsa_circ_21089,RMVar_hsa_circ_351916,RMVar_hsa_circ_332831,RMVar_hsa_circ_323192,RMVar_hsa_circ_330225,RMVar_hsa_circ_247573 8920 RMVar_ID_8920 Human_SNP_ID_333914294 A-to-I Human chr7 - 105273586 105273586 105273586 GGACTGAGATTAGAAAAGTGAGTTGGGTAGCTAGGCGTGGTGGTGCCCACCTGTAATCCCAGCTA GGACTGAGATTAGAAAAGTGAGTTGGGTAGCTGGGCGTGGTGGTGCCCACCTGTAATCCCAGCTA T C SRPK2 Ensembl:ENSG00000135250 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025493400 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15962892 RMVar_hsa_circ_91004,RMVar_hsa_circ_247558,RMVar_hsa_circ_82275,RMVar_hsa_circ_65345,RMVar_hsa_circ_247559,RMVar_hsa_circ_351916,RMVar_hsa_circ_323192,RMVar_hsa_circ_313089,RMVar_hsa_circ_304858 8921 RMVar_ID_8921 Human_SNP_ID_333915090 A-to-I Human chr7 - 105276630 105276630 105276630 GGGCCCAAGTGATCCTGCCATCTCAGCCTCCTAAGTAGCTGAACCACACGTGCATGTCACCATGC GGGCCCAAGTGATCCTGCCATCTCAGCCTCCTGAGTAGCTGAACCACACGTGCATGTCACCATGC T C SRPK2 Ensembl:ENSG00000135250 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1002987395 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91004,RMVar_hsa_circ_247558,RMVar_hsa_circ_82275,RMVar_hsa_circ_65345,RMVar_hsa_circ_247559,RMVar_hsa_circ_351916,RMVar_hsa_circ_323192,RMVar_hsa_circ_313089,RMVar_hsa_circ_304858 8922 RMVar_ID_8922 Human_SNP_ID_333916095 A-to-I Human chr7 - 105280180 105280180 105280180 GAACTTCTGACCTGAAGCAATCTGCCCACTTCAGCCTCCCAAAGTACTGGGGTACAGGCGTGAGC GAACTTCTGACCTGAAGCAATCTGCCCACTTCGGCCTCCCAAAGTACTGGGGTACAGGCGTGAGC T C SRPK2 Ensembl:ENSG00000135250 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs959653515 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91004,RMVar_hsa_circ_247558,RMVar_hsa_circ_82275,RMVar_hsa_circ_65345,RMVar_hsa_circ_247559,RMVar_hsa_circ_351916,RMVar_hsa_circ_323192,RMVar_hsa_circ_313089,RMVar_hsa_circ_304858 8923 RMVar_ID_8923 Human_SNP_ID_333916097 A-to-I Human chr7 - 105280193 105280193 105280193 CCAGGCTGGTTTCGAACTTCTGACCTGAAGCAATCTGCCCACTTCAGCCTCCCAAAGTACTGGGG CCAGGCTGGTTTCGAACTTCTGACCTGAAGCATTCTGCCCACTTCAGCCTCCCAAAGTACTGGGG T A SRPK2 Ensembl:ENSG00000135250 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1192499621 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91004,RMVar_hsa_circ_247558,RMVar_hsa_circ_82275,RMVar_hsa_circ_65345,RMVar_hsa_circ_247559,RMVar_hsa_circ_351916,RMVar_hsa_circ_323192,RMVar_hsa_circ_313089,RMVar_hsa_circ_304858 8924 RMVar_ID_8924 Human_SNP_ID_333916098 A-to-I Human chr7 - 105280193 105280193 105280193 CCAGGCTGGTTTCGAACTTCTGACCTGAAGCAATCTGCCCACTTCAGCCTCCCAAAGTACTGGGG CCAGGCTGGTTTCGAACTTCTGACCTGAAGCAGTCTGCCCACTTCAGCCTCCCAAAGTACTGGGG T C SRPK2 Ensembl:ENSG00000135250 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1192499621 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91004,RMVar_hsa_circ_247558,RMVar_hsa_circ_82275,RMVar_hsa_circ_65345,RMVar_hsa_circ_247559,RMVar_hsa_circ_351916,RMVar_hsa_circ_323192,RMVar_hsa_circ_313089,RMVar_hsa_circ_304858 8925 RMVar_ID_8925 Human_SNP_ID_333920025 A-to-I Human chr7 - 105293212 105293212 105293212 ATCACTACAACCTCCACCTCCCTGGTTCAAGCAGTTATCTTGCCTCAGCCTCTTGAGTAGCTGGG ATCACTACAACCTCCACCTCCCTGGTTCAAGCGGTTATCTTGCCTCAGCCTCTTGAGTAGCTGGG T C SRPK2 Ensembl:ENSG00000135250 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs925451791 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15963310 RMVar_hsa_circ_91004,RMVar_hsa_circ_247558,RMVar_hsa_circ_82275,RMVar_hsa_circ_65345,RMVar_hsa_circ_247559,RMVar_hsa_circ_109183,RMVar_hsa_circ_351916,RMVar_hsa_circ_323192,RMVar_hsa_circ_313089,RMVar_hsa_circ_304858,RMVar_hsa_circ_108754,RMVar_hsa_circ_247574,RMVar_hsa_circ_247575 8926 RMVar_ID_8926 Human_SNP_ID_333925666 A-to-I Human chr7 - 105314318 105314318 105314318 ATTTGCCAGTTTATTTTTCAAGACAGGGTCTTACTCTGTCGTCCAGGCTGGAGTGCAGTGGTGCG ATTTGCCAGTTTATTTTTCAAGACAGGGTCTTCCTCTGTCGTCCAGGCTGGAGTGCAGTGGTGCG T G SRPK2 Ensembl:ENSG00000135250 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285918518 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91004,RMVar_hsa_circ_247558,RMVar_hsa_circ_82275,RMVar_hsa_circ_247559 8927 RMVar_ID_8927 Human_SNP_ID_333927745 A-to-I Human chr7 - 105322223 105322223 105322223 TAGTAGAGGTGGGATTCCACAACATGTTGGCCAGGCGGGTCTCCAACTCCTGACCTCAAGTGATC TAGTAGAGGTGGGATTCCACAACATGTTGGCCCGGCGGGTCTCCAACTCCTGACCTCAAGTGATC T G SRPK2 Ensembl:ENSG00000135250 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941188711 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15964010 RMVar_hsa_circ_91004,RMVar_hsa_circ_247558,RMVar_hsa_circ_82275,RMVar_hsa_circ_247559 8928 RMVar_ID_8928 Human_SNP_ID_333927767 A-to-I Human chr7 - 105322301 105322301 105322301 ACGATTCTCCTGCTTCAGCCTCCTGAGTCACTAGGACCCCAGGCACATGCCCCTATGCCCGGCTA ACGATTCTCCTGCTTCAGCCTCCTGAGTCACTGGGACCCCAGGCACATGCCCCTATGCCCGGCTA T C SRPK2 Ensembl:ENSG00000135250 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1265008141 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_217104 RMVar_hsa_circ_91004,RMVar_hsa_circ_247558,RMVar_hsa_circ_82275,RMVar_hsa_circ_247559 8929 RMVar_ID_8929 Human_SNP_ID_333929530 A-to-I Human chr7 - 105328344 105328344 105328344 TTTGCCAGGCTGGTCTCAAACTCTTGACTTCAAGTGACCCACCCGCCTCGGCTTCCCAAAATGCT TTTGCCAGGCTGGTCTCAAACTCTTGACTTCACGTGACCCACCCGCCTCGGCTTCCCAAAATGCT T G SRPK2 Ensembl:ENSG00000135250 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1359297773 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91004,RMVar_hsa_circ_247558,RMVar_hsa_circ_82275,RMVar_hsa_circ_247559 8930 RMVar_ID_8930 Human_SNP_ID_333935330 A-to-I Human chr7 - 105348244 105348244 105348244 CAACATGGAGAAACCCCGTTTCTATTAACAATACAGAATTGGCCGGGCGTGGTGGCCCATGCCTG CAACATGGAGAAACCCCGTTTCTATTAACAATCCAGAATTGGCCGGGCGTGGTGGCCCATGCCTG T G SRPK2 Ensembl:ENSG00000135250 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1166235441 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91004,RMVar_hsa_circ_247558,RMVar_hsa_circ_82275,RMVar_hsa_circ_247559 8931 RMVar_ID_8931 Human_SNP_ID_333937008 A-to-I Human chr7 - 105353638 105353638 105353638 GGCCTGATGAATTTGCTTGAAGGCAGTCTGTAATCCCATCACTTTGGGAGGCCAAAGAAGGCGGA GGCCTGATGAATTTGCTTGAAGGCAGTCTGTAGTCCCATCACTTTGGGAGGCCAAAGAAGGCGGA T C SRPK2 Ensembl:ENSG00000135250 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs891991749 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24182295 RMVar_hsa_circ_91004,RMVar_hsa_circ_247558,RMVar_hsa_circ_82275,RMVar_hsa_circ_247559 8932 RMVar_ID_8932 Human_SNP_ID_333938481 A-to-I Human chr7 - 105358655 105358655 105358655 GAGACAGGGTCTCTTGTTCTGTTGCCCAGGCTAGAGTGCAGTGGCATGACCTCGTCCTACTGCAA GAGACAGGGTCTCTTGTTCTGTTGCCCAGGCTGGAGTGCAGTGGCATGACCTCGTCCTACTGCAA T C SRPK2 Ensembl:ENSG00000135250 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1218705121 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21404081 RMVar_hsa_circ_91004,RMVar_hsa_circ_247558,RMVar_hsa_circ_82275,RMVar_hsa_circ_247559 8933 RMVar_ID_8933 Human_SNP_ID_333938734 A-to-I Human chr7 - 105359359 105359359 105359359 GGTCAGGACTTCGAGGCCATCCTCACTAACACAGTGAAACCCCATCTCTACTAAAAATAAAAAAA GGTCAGGACTTCGAGGCCATCCTCACTAACACGGTGAAACCCCATCTCTACTAAAAATAAAAAAA T C SRPK2 Ensembl:ENSG00000135250 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1292566966 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91004,RMVar_hsa_circ_247558,RMVar_hsa_circ_82275,RMVar_hsa_circ_247559 8934 RMVar_ID_8934 Human_SNP_ID_333942515 A-to-I Human chr7 - 105372048 105372048 105372048 TCACTGCGGCCTCCGCCTTCCGGGTTCATGCCATTCTCCTGCCTCAGCCTCCTGAGTAACTGGGA TCACTGCGGCCTCCGCCTTCCGGGTTCATGCCGTTCTCCTGCCTCAGCCTCCTGAGTAACTGGGA T C SRPK2 Ensembl:ENSG00000135250 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042612427 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91004,RMVar_hsa_circ_247558,RMVar_hsa_circ_82275,RMVar_hsa_circ_247559 8935 RMVar_ID_8935 Human_SNP_ID_333943093 A-to-I Human chr7 - 105374019 105374018 105374020 GGAGGCTGAGACAGGAGAATCAATTGAACACAAGAGGTAGACGTTGCAGGGAGCCAAGATCATGC GGAGGCTGAGACAGGAGAATCAATTGAACAC__GAGGTAGACGTTGCAGGGAGCCAAGATCATGC CTT C SRPK2 Ensembl:ENSG00000135250 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1210304957 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_15965214,Human_RBP_ID_26056716 RMVar_hsa_circ_91004,RMVar_hsa_circ_247558,RMVar_hsa_circ_82275,RMVar_hsa_circ_247559 8936 RMVar_ID_8936 Human_SNP_ID_333943094 A-to-I Human chr7 - 105374019 105374019 105374019 GGAGGCTGAGACAGGAGAATCAATTGAACACAAGAGGTAGACGTTGCAGGGAGCCAAGATCATGC GGAGGCTGAGACAGGAGAATCAATTGAACACAGGAGGTAGACGTTGCAGGGAGCCAAGATCATGC T C SRPK2 Ensembl:ENSG00000135250 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs945730344 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15965214,Human_RBP_ID_26056716 RMVar_hsa_circ_91004,RMVar_hsa_circ_247558,RMVar_hsa_circ_82275,RMVar_hsa_circ_247559 8937 RMVar_ID_8937 Human_SNP_ID_333943104 A-to-I Human chr7 - 105374056 105374056 105374056 TGGGCGTGGTGGCATGTGCCATAATCCCAGCTACTTGGGAGGCTGAGACAGGAGAATCAATTGAA TGGGCGTGGTGGCATGTGCCATAATCCCAGCTGCTTGGGAGGCTGAGACAGGAGAATCAATTGAA T C SRPK2 Ensembl:ENSG00000135250 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs975745226 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91004,RMVar_hsa_circ_247558,RMVar_hsa_circ_82275,RMVar_hsa_circ_247559 8938 RMVar_ID_8938 Human_SNP_ID_333943305 A-to-I Human chr7 - 105374679 105374679 105374679 ACTGCTTGAACCCGGGAGGTGGAGGTTGTATTAAGCCAGAGATGGCGCCATTGCACTCCAACCTG ACTGCTTGAACCCGGGAGGTGGAGGTTGTATTGAGCCAGAGATGGCGCCATTGCACTCCAACCTG T C SRPK2 Ensembl:ENSG00000135250 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1290826243 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7671647,Human_RBP_ID_15965242,Human_RBP_ID_21951398,Human_RBP_ID_26133180 RMVar_hsa_circ_91004,RMVar_hsa_circ_247558,RMVar_hsa_circ_82275,RMVar_hsa_circ_247559 8939 RMVar_ID_8939 Human_SNP_ID_333943686 A-to-I Human chr7 - 105376056 105376056 105376056 TGGGAAGGCGGAGCTTGCATTGAGCTGAGATCACGACACTGCACTCCAGCCTGGGTGGCAGACAG TGGGAAGGCGGAGCTTGCATTGAGCTGAGATCGCGACACTGCACTCCAGCCTGGGTGGCAGACAG T C SRPK2 Ensembl:ENSG00000135250 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs578258236 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21904703,Human_RBP_ID_26133184 RMVar_hsa_circ_91004,RMVar_hsa_circ_247558,RMVar_hsa_circ_82275,RMVar_hsa_circ_247559 8940 RMVar_ID_8940 Human_SNP_ID_333945365 A-to-I Human chr7 - 105381403 105381403 105381403 ACTGCAGTGGCCTGGTCTTGGCTCACTGAGACAGGGTTTCGCCATATTGGCCAGGCTGGTCTCAA ACTGCAGTGGCCTGGTCTTGGCTCACTGAGACGGGGTTTCGCCATATTGGCCAGGCTGGTCTCAA T C SRPK2 Ensembl:ENSG00000135250 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs967807492 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91004,RMVar_hsa_circ_247558,RMVar_hsa_circ_82275,RMVar_hsa_circ_247559 8941 RMVar_ID_8941 Human_SNP_ID_333976420 A-to-I Human chr7 - 105492005 105492005 105492005 TGGCCCAGGCTGGAGTGCAGCAGAGTGGTCTCAGCTCACTGCAACCTCAGCCTCCTGAGTTCAAG TGGCCCAGGCTGGAGTGCAGCAGAGTGGTCTCGGCTCACTGCAACCTCAGCCTCCTGAGTTCAAG T C PUS7 Ensembl:ENSG00000091127 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1273688397 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_247584,RMVar_hsa_circ_285289,RMVar_hsa_circ_348222,RMVar_hsa_circ_272262,RMVar_hsa_circ_91963,RMVar_hsa_circ_247585,RMVar_hsa_circ_247598,RMVar_hsa_circ_337664,RMVar_hsa_circ_247583,RMVar_hsa_circ_364623,RMVar_hsa_circ_303153,RMVar_hsa_circ_290844,RMVar_hsa_circ_247600,RMVar_hsa_circ_247599,RMVar_hsa_circ_316206,RMVar_hsa_circ_369206,RMVar_hsa_circ_335614,RMVar_hsa_circ_24152,RMVar_hsa_circ_265423,RMVar_hsa_circ_315611,RMVar_hsa_circ_247605,RMVar_hsa_circ_281914,RMVar_hsa_circ_278661,RMVar_hsa_circ_65542,RMVar_hsa_circ_247606,RMVar_hsa_circ_374055,RMVar_hsa_circ_272700,RMVar_hsa_circ_53467,RMVar_hsa_circ_247609,RMVar_hsa_circ_247610,RMVar_hsa_circ_247608,RMVar_hsa_circ_247613,RMVar_hsa_circ_280258,RMVar_hsa_circ_289174,RMVar_hsa_circ_303818,RMVar_hsa_circ_348168,RMVar_hsa_circ_304172,RMVar_hsa_circ_286928,RMVar_hsa_circ_247615,RMVar_hsa_circ_247616,RMVar_hsa_circ_247614,RMVar_hsa_circ_247622,RMVar_hsa_circ_247611,RMVar_hsa_circ_247612,RMVar_hsa_circ_312275,RMVar_hsa_circ_317114,RMVar_hsa_circ_319086,RMVar_hsa_circ_312314,RMVar_hsa_circ_247623,RMVar_hsa_circ_247620,RMVar_hsa_circ_247621 8942 RMVar_ID_8942 Human_SNP_ID_333977240 A-to-I Human chr7 - 105494881 105494881 105494881 GCCTTGACTTCCTGGGCTCAGGCATTCCTCCTACCTTAGCCTCCTGAGTAGCTGGGATTACAGGC GCCTTGACTTCCTGGGCTCAGGCATTCCTCCTGCCTTAGCCTCCTGAGTAGCTGGGATTACAGGC T C PUS7 Ensembl:ENSG00000091127 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs554301481 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_247584,RMVar_hsa_circ_285289,RMVar_hsa_circ_348222,RMVar_hsa_circ_272262,RMVar_hsa_circ_91963,RMVar_hsa_circ_247585,RMVar_hsa_circ_247598,RMVar_hsa_circ_337664,RMVar_hsa_circ_247583,RMVar_hsa_circ_364623,RMVar_hsa_circ_303153,RMVar_hsa_circ_290844,RMVar_hsa_circ_247600,RMVar_hsa_circ_247599,RMVar_hsa_circ_316206,RMVar_hsa_circ_369206,RMVar_hsa_circ_335614,RMVar_hsa_circ_24152,RMVar_hsa_circ_265423,RMVar_hsa_circ_315611,RMVar_hsa_circ_247605,RMVar_hsa_circ_281914,RMVar_hsa_circ_278661,RMVar_hsa_circ_65542,RMVar_hsa_circ_247606,RMVar_hsa_circ_374055,RMVar_hsa_circ_272700,RMVar_hsa_circ_53467,RMVar_hsa_circ_247609,RMVar_hsa_circ_247610,RMVar_hsa_circ_247608,RMVar_hsa_circ_247613,RMVar_hsa_circ_280258,RMVar_hsa_circ_289174,RMVar_hsa_circ_303818,RMVar_hsa_circ_348168,RMVar_hsa_circ_304172,RMVar_hsa_circ_286928,RMVar_hsa_circ_247615,RMVar_hsa_circ_247616,RMVar_hsa_circ_247614,RMVar_hsa_circ_247622,RMVar_hsa_circ_247611,RMVar_hsa_circ_247612,RMVar_hsa_circ_312275,RMVar_hsa_circ_317114,RMVar_hsa_circ_319086,RMVar_hsa_circ_312314,RMVar_hsa_circ_247623,RMVar_hsa_circ_247620,RMVar_hsa_circ_247621 8943 RMVar_ID_8943 Human_SNP_ID_333977264 A-to-I Human chr7 - 105494973 105494973 105494973 CTTTCTTTCTTTCTTTTTTTTTTTTTTTTTTTAGACAGTCTCACTCTGTCACTCAGGCTGGAGTG CTTTCTTTCTTTCTTTTTTTTTTTTTTTTTTTTGACAGTCTCACTCTGTCACTCAGGCTGGAGTG T A PUS7 Ensembl:ENSG00000091127 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1469607465 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21404208 RMVar_hsa_circ_247584,RMVar_hsa_circ_285289,RMVar_hsa_circ_348222,RMVar_hsa_circ_272262,RMVar_hsa_circ_91963,RMVar_hsa_circ_247585,RMVar_hsa_circ_247598,RMVar_hsa_circ_337664,RMVar_hsa_circ_247583,RMVar_hsa_circ_364623,RMVar_hsa_circ_303153,RMVar_hsa_circ_290844,RMVar_hsa_circ_247600,RMVar_hsa_circ_247599,RMVar_hsa_circ_316206,RMVar_hsa_circ_369206,RMVar_hsa_circ_335614,RMVar_hsa_circ_24152,RMVar_hsa_circ_265423,RMVar_hsa_circ_315611,RMVar_hsa_circ_247605,RMVar_hsa_circ_281914,RMVar_hsa_circ_278661,RMVar_hsa_circ_65542,RMVar_hsa_circ_247606,RMVar_hsa_circ_374055,RMVar_hsa_circ_272700,RMVar_hsa_circ_53467,RMVar_hsa_circ_247609,RMVar_hsa_circ_247610,RMVar_hsa_circ_247608,RMVar_hsa_circ_247613,RMVar_hsa_circ_280258,RMVar_hsa_circ_289174,RMVar_hsa_circ_303818,RMVar_hsa_circ_348168,RMVar_hsa_circ_304172,RMVar_hsa_circ_286928,RMVar_hsa_circ_247615,RMVar_hsa_circ_247616,RMVar_hsa_circ_247614,RMVar_hsa_circ_247622,RMVar_hsa_circ_247611,RMVar_hsa_circ_247612,RMVar_hsa_circ_312275,RMVar_hsa_circ_317114,RMVar_hsa_circ_319086,RMVar_hsa_circ_312314,RMVar_hsa_circ_247623,RMVar_hsa_circ_247620,RMVar_hsa_circ_247621 8944 RMVar_ID_8944 Human_SNP_ID_333977265 A-to-I Human chr7 - 105494973 105494973 105494973 CTTTCTTTCTTTCTTTTTTTTTTTTTTTTTTTAGACAGTCTCACTCTGTCACTCAGGCTGGAGTG CTTTCTTTCTTTCTTTTTTTTTTTTTTTTTTTGGACAGTCTCACTCTGTCACTCAGGCTGGAGTG T C PUS7 Ensembl:ENSG00000091127 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1469607465 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21404208 RMVar_hsa_circ_247584,RMVar_hsa_circ_285289,RMVar_hsa_circ_348222,RMVar_hsa_circ_272262,RMVar_hsa_circ_91963,RMVar_hsa_circ_247585,RMVar_hsa_circ_247598,RMVar_hsa_circ_337664,RMVar_hsa_circ_247583,RMVar_hsa_circ_364623,RMVar_hsa_circ_303153,RMVar_hsa_circ_290844,RMVar_hsa_circ_247600,RMVar_hsa_circ_247599,RMVar_hsa_circ_316206,RMVar_hsa_circ_369206,RMVar_hsa_circ_335614,RMVar_hsa_circ_24152,RMVar_hsa_circ_265423,RMVar_hsa_circ_315611,RMVar_hsa_circ_247605,RMVar_hsa_circ_281914,RMVar_hsa_circ_278661,RMVar_hsa_circ_65542,RMVar_hsa_circ_247606,RMVar_hsa_circ_374055,RMVar_hsa_circ_272700,RMVar_hsa_circ_53467,RMVar_hsa_circ_247609,RMVar_hsa_circ_247610,RMVar_hsa_circ_247608,RMVar_hsa_circ_247613,RMVar_hsa_circ_280258,RMVar_hsa_circ_289174,RMVar_hsa_circ_303818,RMVar_hsa_circ_348168,RMVar_hsa_circ_304172,RMVar_hsa_circ_286928,RMVar_hsa_circ_247615,RMVar_hsa_circ_247616,RMVar_hsa_circ_247614,RMVar_hsa_circ_247622,RMVar_hsa_circ_247611,RMVar_hsa_circ_247612,RMVar_hsa_circ_312275,RMVar_hsa_circ_317114,RMVar_hsa_circ_319086,RMVar_hsa_circ_312314,RMVar_hsa_circ_247623,RMVar_hsa_circ_247620,RMVar_hsa_circ_247621 8945 RMVar_ID_8945 Human_SNP_ID_333989422 A-to-I Human chr7 + 105537304 105537304 105537304 AGGCATGTGTCACCCTGCCCAGCTAATTTTGTATTTTAGGTAGAGATGGGGTTTCATCATGTTGG AGGCATGTGTCACCCTGCCCAGCTAATTTTGTGTTTTAGGTAGAGATGGGGTTTCATCATGTTGG A G RINT1 Ensembl:ENSG00000135249 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1401639660 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_146,RMVar_hsa_circ_100679,RMVar_hsa_circ_77844,RMVar_hsa_circ_247627,RMVar_hsa_circ_247628,RMVar_hsa_circ_55170,RMVar_hsa_circ_317355,RMVar_hsa_circ_331991,RMVar_hsa_circ_305592,RMVar_hsa_circ_247629,RMVar_hsa_circ_247630,RMVar_hsa_circ_247631 8946 RMVar_ID_8946 Human_SNP_ID_333990332 A-to-I Human chr7 + 105540962 105540962 105540962 CGGGTTTAAGAAATTCTCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTATGTGCCACCATG CGGGTTTAAGAAATTCTCTGCCTCAGCCTCCCGAAGTGCTGGGATTACAGGTATGTGCCACCATG A G RINT1 Ensembl:ENSG00000135249 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1481197760 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_146,RMVar_hsa_circ_100679,RMVar_hsa_circ_77844,RMVar_hsa_circ_247627,RMVar_hsa_circ_247628,RMVar_hsa_circ_55170,RMVar_hsa_circ_317355,RMVar_hsa_circ_331991,RMVar_hsa_circ_305592,RMVar_hsa_circ_247629,RMVar_hsa_circ_247630,RMVar_hsa_circ_247631 8947 RMVar_ID_8947 Human_SNP_ID_333990441 A-to-I Human chr7 + 105541317 105541317 105541317 TGCCACCAAACCTGGCTAGTTTTTGTATTTTTAGTAGAGATGGGGTTTCATCATGTTGGCCAGGC TGCCACCAAACCTGGCTAGTTTTTGTATTTTTCGTAGAGATGGGGTTTCATCATGTTGGCCAGGC A C RINT1 Ensembl:ENSG00000135249 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs545405200 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_146,RMVar_hsa_circ_100679,RMVar_hsa_circ_77844,RMVar_hsa_circ_247627,RMVar_hsa_circ_247628,RMVar_hsa_circ_55170,RMVar_hsa_circ_317355,RMVar_hsa_circ_331991,RMVar_hsa_circ_305592,RMVar_hsa_circ_247629,RMVar_hsa_circ_247630,RMVar_hsa_circ_247631 8948 RMVar_ID_8948 Human_SNP_ID_333990516 A-to-I Human chr7 + 105541599 105541599 105541599 GGAGTTCGAGATCAGCCTGACCAACGTGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGC GGAGTTCGAGATCAGCCTGACCAACGTGGTGACACCCCGTCTCTACTAAAAATACAAAAATTAGC A C RINT1 Ensembl:ENSG00000135249 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs924414404 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_146,RMVar_hsa_circ_100679,RMVar_hsa_circ_77844,RMVar_hsa_circ_247627,RMVar_hsa_circ_247628,RMVar_hsa_circ_55170,RMVar_hsa_circ_317355,RMVar_hsa_circ_331991,RMVar_hsa_circ_305592,RMVar_hsa_circ_247629,RMVar_hsa_circ_247630,RMVar_hsa_circ_247631 8949 RMVar_ID_8949 Human_SNP_ID_333990529 A-to-I Human chr7 + 105541665 105541665 105541665 GAGCGTGATGGCACGTGTCTATAATTCCTGCTATTTAGGAGGCTGAGGCAGGAGAATCACTTGAC GAGCGTGATGGCACGTGTCTATAATTCCTGCTGTTTAGGAGGCTGAGGCAGGAGAATCACTTGAC A G RINT1 Ensembl:ENSG00000135249 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1387761863 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_146,RMVar_hsa_circ_100679,RMVar_hsa_circ_77844,RMVar_hsa_circ_247627,RMVar_hsa_circ_247628,RMVar_hsa_circ_55170,RMVar_hsa_circ_317355,RMVar_hsa_circ_331991,RMVar_hsa_circ_305592,RMVar_hsa_circ_247629,RMVar_hsa_circ_247630,RMVar_hsa_circ_247631 8950 RMVar_ID_8950 Human_SNP_ID_333991442 A-to-I Human chr7 + 105545341 105545341 105545341 AGGCTTGGTGGTGAGCACCCATAGTCCCAGCTACTCGGGAGGCTGAGGTAGGAGGATCGCTTGAG AGGCTTGGTGGTGAGCACCCATAGTCCCAGCTGCTCGGGAGGCTGAGGTAGGAGGATCGCTTGAG A G RINT1 Ensembl:ENSG00000135249 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs944411528 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26057459 RMVar_hsa_circ_146,RMVar_hsa_circ_100679,RMVar_hsa_circ_77844,RMVar_hsa_circ_247627,RMVar_hsa_circ_247628,RMVar_hsa_circ_55170,RMVar_hsa_circ_317355,RMVar_hsa_circ_305592,RMVar_hsa_circ_34036,RMVar_hsa_circ_312948,RMVar_hsa_circ_247629,RMVar_hsa_circ_247630,RMVar_hsa_circ_247631,RMVar_hsa_circ_320331,RMVar_hsa_circ_319342,RMVar_hsa_circ_284797,RMVar_hsa_circ_312194,RMVar_hsa_circ_58218,RMVar_hsa_circ_247633,RMVar_hsa_circ_247635,RMVar_hsa_circ_247636,RMVar_hsa_circ_247634,RMVar_hsa_circ_247632 8951 RMVar_ID_8951 Human_SNP_ID_333991862 A-to-I Human chr7 + 105546765 105546765 105546765 AGGCATGGGGGCGCATGCCTGTAATCCCAGCTACTGTGGAGGCTGAGGCGGGAGAATCACTTGAA AGGCATGGGGGCGCATGCCTGTAATCCCAGCTGCTGTGGAGGCTGAGGCGGGAGAATCACTTGAA A G RINT1 Ensembl:ENSG00000135249 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs185831648 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_146,RMVar_hsa_circ_100679,RMVar_hsa_circ_77844,RMVar_hsa_circ_247627,RMVar_hsa_circ_247628,RMVar_hsa_circ_55170,RMVar_hsa_circ_317355,RMVar_hsa_circ_305592,RMVar_hsa_circ_34036,RMVar_hsa_circ_312948,RMVar_hsa_circ_247629,RMVar_hsa_circ_247630,RMVar_hsa_circ_247631,RMVar_hsa_circ_320331,RMVar_hsa_circ_319342,RMVar_hsa_circ_284797,RMVar_hsa_circ_312194,RMVar_hsa_circ_58218,RMVar_hsa_circ_247633,RMVar_hsa_circ_247635,RMVar_hsa_circ_247636,RMVar_hsa_circ_247634,RMVar_hsa_circ_247632 8952 RMVar_ID_8952 Human_SNP_ID_333991872 A-to-I Human chr7 + 105546796 105546796 105546796 TACTGTGGAGGCTGAGGCGGGAGAATCACTTGAACCTGGGACACAGAATTTGCATTGAGCCAAAT TACTGTGGAGGCTGAGGCGGGAGAATCACTTGTACCTGGGACACAGAATTTGCATTGAGCCAAAT A T RINT1 Ensembl:ENSG00000135249 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1456981117 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_146,RMVar_hsa_circ_100679,RMVar_hsa_circ_77844,RMVar_hsa_circ_247627,RMVar_hsa_circ_247628,RMVar_hsa_circ_55170,RMVar_hsa_circ_317355,RMVar_hsa_circ_305592,RMVar_hsa_circ_34036,RMVar_hsa_circ_312948,RMVar_hsa_circ_247629,RMVar_hsa_circ_247630,RMVar_hsa_circ_247631,RMVar_hsa_circ_320331,RMVar_hsa_circ_319342,RMVar_hsa_circ_284797,RMVar_hsa_circ_312194,RMVar_hsa_circ_58218,RMVar_hsa_circ_247633,RMVar_hsa_circ_247635,RMVar_hsa_circ_247636,RMVar_hsa_circ_247634,RMVar_hsa_circ_247632 8953 RMVar_ID_8953 Human_SNP_ID_333995435 A-to-I Human chr7 + 105560850 105560850 105560850 TCAAGTTATTCTCCTGCCTCAGCTTCCTGAGTAGCTGGGATTACAGGTGTGCGCCACCATGCCCG TCAAGTTATTCTCCTGCCTCAGCTTCCTGAGTGGCTGGGATTACAGGTGTGCGCCACCATGCCCG A G RINT1 Ensembl:ENSG00000135249 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs760833975 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_146,RMVar_hsa_circ_100679,RMVar_hsa_circ_77844,RMVar_hsa_circ_247627,RMVar_hsa_circ_247628,RMVar_hsa_circ_109805,RMVar_hsa_circ_312948,RMVar_hsa_circ_247629,RMVar_hsa_circ_312194,RMVar_hsa_circ_247635,RMVar_hsa_circ_247636,RMVar_hsa_circ_66917,RMVar_hsa_circ_247639,RMVar_hsa_circ_60829,RMVar_hsa_circ_299704,RMVar_hsa_circ_338022,RMVar_hsa_circ_348331,RMVar_hsa_circ_247643,RMVar_hsa_circ_247644,RMVar_hsa_circ_247642 8954 RMVar_ID_8954 Human_SNP_ID_333995445 A-to-I Human chr7 + 105560901 105560901 105560901 CGCCACCATGCCCGACTAACTTTTCTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGTCAGGC CGCCACCATGCCCGACTAACTTTTCTATTTTTGGTAGAGATGGGGTTTCACCATGTTGGTCAGGC A G RINT1 Ensembl:ENSG00000135249 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs954165692 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_146,RMVar_hsa_circ_100679,RMVar_hsa_circ_77844,RMVar_hsa_circ_247627,RMVar_hsa_circ_247628,RMVar_hsa_circ_109805,RMVar_hsa_circ_312948,RMVar_hsa_circ_247629,RMVar_hsa_circ_312194,RMVar_hsa_circ_247635,RMVar_hsa_circ_247636,RMVar_hsa_circ_66917,RMVar_hsa_circ_247639,RMVar_hsa_circ_60829,RMVar_hsa_circ_299704,RMVar_hsa_circ_338022,RMVar_hsa_circ_348331,RMVar_hsa_circ_247643,RMVar_hsa_circ_247644,RMVar_hsa_circ_247642 8955 RMVar_ID_8955 Human_SNP_ID_333996089 A-to-I Human chr7 + 105563440 105563440 105563440 TGGAGTGCAGAGGCATGATCTCGGCTCACTGCAACTTCCACCTTCCAGGTTCAAGCTAGGATTAC TGGAGTGCAGAGGCATGATCTCGGCTCACTGCGACTTCCACCTTCCAGGTTCAAGCTAGGATTAC A G RINT1 Ensembl:ENSG00000135249 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956039422 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_146,RMVar_hsa_circ_100679,RMVar_hsa_circ_77844,RMVar_hsa_circ_247627,RMVar_hsa_circ_247628,RMVar_hsa_circ_109805,RMVar_hsa_circ_312948,RMVar_hsa_circ_247629,RMVar_hsa_circ_312194,RMVar_hsa_circ_247635,RMVar_hsa_circ_247636,RMVar_hsa_circ_66917,RMVar_hsa_circ_247639,RMVar_hsa_circ_60829,RMVar_hsa_circ_299704,RMVar_hsa_circ_338022,RMVar_hsa_circ_348331,RMVar_hsa_circ_247643,RMVar_hsa_circ_247644,RMVar_hsa_circ_247642 8956 RMVar_ID_8956 Human_SNP_ID_334037345 A-to-I Human chr7 - 105724282 105724282 105724282 GGTGTGAACCACTGCGCCCGGCCCTAATTTCCATTTCTGATTAAACAGCAGCACAGAAAATTATC GGTGTGAACCACTGCGCCCGGCCCTAATTTCCCTTTCTGATTAAACAGCAGCACAGAAAATTATC T G ATXN7L1 Ensembl:ENSG00000146776 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs967146541 Functional Loss SNV dbSNP153 33..33 33 - - - 8957 RMVar_ID_8957 Human_SNP_ID_334037911 A-to-I Human chr7 - 105726274 105726274 105726274 CTTCTTTGTGCTCTTGGAATTATTTCCTACATAGTTGGAAGTTTGGATGGATGTGTGAAAGCTTA CTTCTTTGTGCTCTTGGAATTATTTCCTACATGGTTGGAAGTTTGGATGGATGTGTGAAAGCTTA T C ATXN7L1 Ensembl:ENSG00000146776 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1019825378 Functional Loss SNV dbSNP153 33..33 33 - - - 8958 RMVar_ID_8958 Human_SNP_ID_334037912 A-to-I Human chr7 - 105726276 105726276 105726276 GCCTTCTTTGTGCTCTTGGAATTATTTCCTACATAGTTGGAAGTTTGGATGGATGTGTGAAAGCT GCCTTCTTTGTGCTCTTGGAATTATTTCCTACGTAGTTGGAAGTTTGGATGGATGTGTGAAAGCT T C ATXN7L1 Ensembl:ENSG00000146776 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900048706 Functional Loss SNV dbSNP153 33..33 33 - - - 8959 RMVar_ID_8959 Human_SNP_ID_334066402 A-to-I Human chr7 - 105846532 105846532 105846532 AGAACTGTGAAACTGTTTTCTAAAGCAGCCGCACCATTTTAAATTCCCACCAACAATGTATGAGG AGAACTGTGAAACTGTTTTCTAAAGCAGCCGCGCCATTTTAAATTCCCACCAACAATGTATGAGG T C ATXN7L1 Ensembl:ENSG00000146776 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1171759207 Functional Loss SNV dbSNP153 33..33 33 - - - 8960 RMVar_ID_8960 Human_SNP_ID_334069335 A-to-I Human chr7 - 105859875 105859875 105859875 GGGAGGCCGAGGTGGGAGAAATGCTTGAGCCCAGGAGGCAGAGGTTGGAGTGAGCTGAGATCGTG GGGAGGCCGAGGTGGGAGAAATGCTTGAGCCCGGGAGGCAGAGGTTGGAGTGAGCTGAGATCGTG T C ATXN7L1 Ensembl:ENSG00000146776 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1183806053 Functional Loss SNV dbSNP153 33..33 33 - - - 8961 RMVar_ID_8961 Human_SNP_ID_334129642 A-to-I Human chr7 - 106109956 106109956 106109956 ATAATTCCTCAATCAATCGATTTCTCCCTCCAATTCTGACCTTTCCAATCCATCCCTCTAACTGC ATAATTCCTCAATCAATCGATTTCTCCCTCCAGTTCTGACCTTTCCAATCCATCCCTCTAACTGC T C SYPL1 Ensembl:ENSG00000008282 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334238320 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123488,RMVar_hsa_circ_247669,RMVar_hsa_circ_325508,RMVar_hsa_circ_247674,RMVar_hsa_circ_313455,RMVar_hsa_circ_122868,RMVar_hsa_circ_247675 8962 RMVar_ID_8962 Human_SNP_ID_334129654 A-to-I Human chr7 - 106110002 106110002 106110002 TTAAAGGCTTTAAACAAGTCAATGATACGACTAATTTTAGGCACTCATAATTCCTCAATCAATCG TTAAAGGCTTTAAACAAGTCAATGATACGACTGATTTTAGGCACTCATAATTCCTCAATCAATCG T C SYPL1 Ensembl:ENSG00000008282 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1360570591 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123488,RMVar_hsa_circ_247669,RMVar_hsa_circ_325508,RMVar_hsa_circ_247674,RMVar_hsa_circ_313455,RMVar_hsa_circ_122868,RMVar_hsa_circ_247675 8963 RMVar_ID_8963 Human_SNP_ID_334397598 A-to-I Human chr7 + 107171815 107171815 107171815 CCGGGAGGCAGAGATTGCAGTGAGACAAGATCAGGCCACTGTACTCCAGCCTGGGCATCAGAACG CCGGGAGGCAGAGATTGCAGTGAGACAAGATCGGGCCACTGTACTCCAGCCTGGGCATCAGAACG A G HBP1 Ensembl:ENSG00000105856 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1222640529 Functional Loss SNV dbSNP153 33..33 33 - - - 8964 RMVar_ID_8964 Human_SNP_ID_334397767 A-to-I Human chr7 + 107172408 107172408 107172408 GTGAACCACATTATGGAGAAAATTATGTTTCTAGTTTCTCCATAGAAAATGATAATAGAAATTAT GTGAACCACATTATGGAGAAAATTATGTTTCTGGTTTCTCCATAGAAAATGATAATAGAAATTAT A G HBP1 Ensembl:ENSG00000105856 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1228865991 Functional Loss SNV dbSNP153 33..33 33 - - - 8965 RMVar_ID_8965 Human_SNP_ID_334405629 A-to-I Human chr7 + 107201866 107201866 107201866 TAATCTGTATTGTACACATGATGAAATGAAGCAGAAGCTGGGAGTCGGCCTTTCCTCTAGTAACC TAATCTGTATTGTACACATGATGAAATGAAGCTGAAGCTGGGAGTCGGCCTTTCCTCTAGTAACC A T HBP1 Ensembl:ENSG00000105856 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1352106384 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7673262 RMVar_hsa_circ_247703 8966 RMVar_ID_8966 Human_SNP_ID_334406139 A-to-I Human chr7 - 107203593 107203593 107203593 CCCTGGAAGCTTATGTTCAATCAGTGAGAAGTAGAGAAGGCAAAGAATTTGCACCAGTTTATCCC CCCTGGAAGCTTATGTTCAATCAGTGAGAAGTCGAGAAGGCAAAGAATTTGCACCAGTTTATCCC T G COG5 Ensembl:ENSG00000164597 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1215259556 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15969462,Human_RBP_ID_22464693,Human_RBP_ID_26130673 Human_Splice_Rec_908272,Human_Splice_Rec_908314 8967 RMVar_ID_8967 Human_SNP_ID_334421764 A-to-I Human chr7 - 107265398 107265398 107265398 TGGTATATGCCTGTGGTCCCAGCTACTCGGGAAGCTGAGATGGGAGGATCACTTGATCAGGAGGT TGGTATATGCCTGTGGTCCCAGCTACTCGGGATGCTGAGATGGGAGGATCACTTGATCAGGAGGT T A COG5 Ensembl:ENSG00000164597 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs752330882 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10029,RMVar_hsa_circ_55396,RMVar_hsa_circ_61731,RMVar_hsa_circ_347228,RMVar_hsa_circ_375594,RMVar_hsa_circ_360761,RMVar_hsa_circ_304678,RMVar_hsa_circ_68764,RMVar_hsa_circ_247708,RMVar_hsa_circ_247709,RMVar_hsa_circ_247707,RMVar_hsa_circ_247713,RMVar_hsa_circ_284075,RMVar_hsa_circ_46824,RMVar_hsa_circ_350534,RMVar_hsa_circ_247714 8968 RMVar_ID_8968 Human_SNP_ID_334421914 A-to-I Human chr7 - 107266040 107266038 107266040 TATTATTATTGTTGTTATTATTATTTGGAGACAGGGTCTGTCACCCAGGCTGGAGTGCAGTGATA TATTATTATTGTTGTTATTATTATTTGGAGAC__GGTCTGTCACCCAGGCTGGAGTGCAGTGATA CCT C COG5 Ensembl:ENSG00000164597 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474927369 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_7673489 RMVar_hsa_circ_10029,RMVar_hsa_circ_55396,RMVar_hsa_circ_61731,RMVar_hsa_circ_347228,RMVar_hsa_circ_375594,RMVar_hsa_circ_360761,RMVar_hsa_circ_304678,RMVar_hsa_circ_68764,RMVar_hsa_circ_247708,RMVar_hsa_circ_247709,RMVar_hsa_circ_247707,RMVar_hsa_circ_247713,RMVar_hsa_circ_284075,RMVar_hsa_circ_46824,RMVar_hsa_circ_350534,RMVar_hsa_circ_247714 8969 RMVar_ID_8969 Human_SNP_ID_334471696 A-to-I Human chr7 - 107457703 107457703 107457703 ATTTTAGGCCGGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGGGG ATTTTAGGCCGGGCGCAGTGGCTCACGCCTGTTATCCCAGCACTTTGGGAGGCTGAGGCGGGGGG T A COG5 Ensembl:ENSG00000164597 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs951321572 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10029,RMVar_hsa_circ_95997,RMVar_hsa_circ_247719,RMVar_hsa_circ_2451,RMVar_hsa_circ_37508,RMVar_hsa_circ_341486 8970 RMVar_ID_8970 Human_SNP_ID_334472124 A-to-I Human chr7 - 107459552 107459552 107459552 GTCTCAAGGATCCTCCTGCCCTGGCCTCTCAAAGTGCTGGAATTACAGTCGTGAGCCACCACACC GTCTCAAGGATCCTCCTGCCCTGGCCTCTCAAGGTGCTGGAATTACAGTCGTGAGCCACCACACC T C COG5 Ensembl:ENSG00000164597 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs921342100 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10029,RMVar_hsa_circ_95997,RMVar_hsa_circ_247719,RMVar_hsa_circ_2451,RMVar_hsa_circ_37508,RMVar_hsa_circ_341486 8971 RMVar_ID_8971 Human_SNP_ID_334513678 A-to-I Human chr7 + 107616800 107616800 107616800 TCACTCTGTCACCAAGACTGGAGTTCAGTGGCACAATCTCAGCTCGCTGCAACCTCCACCTCCCC TCACTCTGTCACCAAGACTGGAGTTCAGTGGCGCAATCTCAGCTCGCTGCAACCTCCACCTCCCC A G BCAP29,DUS4L-BCAP29 Ensembl:ENSG00000075790,Ensembl:ENSG00000288558 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1246258433 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110043,RMVar_hsa_circ_247738,RMVar_hsa_circ_78982,RMVar_hsa_circ_247740 8972 RMVar_ID_8972 Human_SNP_ID_334513706 A-to-I Human chr7 + 107616878 107616878 107616878 CTTGTGCCTCAGCCTTCTGAGTGACTGGGACTACAAGCACATGCCACCATGCGCAGCTAAGTTGG CTTGTGCCTCAGCCTTCTGAGTGACTGGGACTGCAAGCACATGCCACCATGCGCAGCTAAGTTGG A G BCAP29,DUS4L-BCAP29 Ensembl:ENSG00000075790,Ensembl:ENSG00000288558 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1057072972 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110043,RMVar_hsa_circ_247738,RMVar_hsa_circ_78982,RMVar_hsa_circ_247740 8973 RMVar_ID_8973 Human_SNP_ID_334513707 A-to-I Human chr7 + 107616880 107616880 107616880 TGTGCCTCAGCCTTCTGAGTGACTGGGACTACAAGCACATGCCACCATGCGCAGCTAAGTTGGGT TGTGCCTCAGCCTTCTGAGTGACTGGGACTACGAGCACATGCCACCATGCGCAGCTAAGTTGGGT A G BCAP29,DUS4L-BCAP29 Ensembl:ENSG00000075790,Ensembl:ENSG00000288558 Protein coding,Protein coding intron,intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs915538581 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110043,RMVar_hsa_circ_247738,RMVar_hsa_circ_78982,RMVar_hsa_circ_247740 8974 RMVar_ID_8974 Human_SNP_ID_334596191 A-to-I Human chr7 + 107919877 107919877 107919877 TGAAGGGTAATTATATAGTTACCCAAATTAAGAGAGTCTATTTACGGAACTCAAATACGTGGGCA TGAAGGGTAATTATATAGTTACCCAAATTAAGGGAGTCTATTTACGGAACTCAAATACGTGGGCA A G DLD Ensembl:ENSG00000091140 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1354089565 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_672848,Human_RBP_ID_1680320,Human_RBP_ID_2032965,Human_RBP_ID_3826370,Human_RBP_ID_15973069,Human_RBP_ID_17423586,Human_RBP_ID_17538741,Human_RBP_ID_18376678,Human_RBP_ID_24183572,Human_RBP_ID_24514324,Human_RBP_ID_27762019 8975 RMVar_ID_8975 Human_SNP_ID_334605377 A-to-I Human chr7 - 107954269 107954269 107954269 AAACCTGTAGTCCCAGCTGCTGGGAAAGCTGAAGTGGGAGAATTCCTTGAGCCCGGAAATTCAGG AAACCTGTAGTCCCAGCTGCTGGGAAAGCTGAGGTGGGAGAATTCCTTGAGCCCGGAAATTCAGG T C LAMB1 Ensembl:ENSG00000091136 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1346756341 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111523,RMVar_hsa_circ_102534,RMVar_hsa_circ_247756,RMVar_hsa_circ_82203,RMVar_hsa_circ_247757,RMVar_hsa_circ_99230,RMVar_hsa_circ_247760,RMVar_hsa_circ_247759,RMVar_hsa_circ_247764,RMVar_hsa_circ_91805,RMVar_hsa_circ_307346,RMVar_hsa_circ_123552,RMVar_hsa_circ_102722,RMVar_hsa_circ_247766,RMVar_hsa_circ_87830,RMVar_hsa_circ_247767,RMVar_hsa_circ_247765,RMVar_hsa_circ_247763,RMVar_hsa_circ_75604,RMVar_hsa_circ_247769,RMVar_hsa_circ_326485,RMVar_hsa_circ_342147,RMVar_hsa_circ_371502,RMVar_hsa_circ_372813,RMVar_hsa_circ_326885,RMVar_hsa_circ_111386,RMVar_hsa_circ_113301,RMVar_hsa_circ_102395,RMVar_hsa_circ_247773,RMVar_hsa_circ_247775,RMVar_hsa_circ_38398,RMVar_hsa_circ_247776,RMVar_hsa_circ_247774,RMVar_hsa_circ_247771,RMVar_hsa_circ_247772,RMVar_hsa_circ_374536,RMVar_hsa_circ_247770,RMVar_hsa_circ_347821,RMVar_hsa_circ_247778,RMVar_hsa_circ_247780,RMVar_hsa_circ_115182,RMVar_hsa_circ_247779 8976 RMVar_ID_8976 Human_SNP_ID_334722886 A-to-I Human chr7 - 108432786 108432786 108432786 GCCATCCTCCTGTCTCATGCTTCCTAGTAGCTAGGACTATAGGTGCGTACCACCACACTTGGCTG GCCATCCTCCTGTCTCATGCTTCCTAGTAGCTGGGACTATAGGTGCGTACCACCACACTTGGCTG T C NRCAM Ensembl:ENSG00000091129 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1403092555 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266485 8977 RMVar_ID_8977 Human_SNP_ID_334754462 A-to-I Human chr7 - 108561342 108561342 108561342 GGAGGATTGCTTGAGCTCAGGAGGTAGAGCCTACAATGGGCTGAGATCGTGCCACTGCATTCCAG GGAGGATTGCTTGAGCTCAGGAGGTAGAGCCTGCAATGGGCTGAGATCGTGCCACTGCATTCCAG T C PNPLA8,THAP5 Ensembl:ENSG00000135241,Ensembl:ENSG00000177683 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560270482 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15973990 8978 RMVar_ID_8978 Human_SNP_ID_334754921 A-to-I Human chr7 - 108563476 108563476 108563476 TGGAGTGCAGTGGCCTGATCTTGGCTCACTGCAGCCTCTGCCTCCCGGGTTCAAGTGATTCTTCT TGGAGTGCAGTGGCCTGATCTTGGCTCACTGCGGCCTCTGCCTCCCGGGTTCAAGTGATTCTTCT T C PNPLA8,THAP5 Ensembl:ENSG00000135241,Ensembl:ENSG00000177683 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs770493884 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23080936 8979 RMVar_ID_8979 Human_SNP_ID_335153780 A-to-I Human chr7 - 110107838 110107838 110107838 CAGTGTTTATAAAGTCCAAGGTAGTTACAGTAATGTCCTAGGCCTTCATATTCACTCACTCTGAC CAGTGTTTATAAAGTCCAAGGTAGTTACAGTAGTGTCCTAGGCCTTCATATTCACTCACTCTGAC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1398102294 Functional Loss SNV dbSNP153 33..33 33 - - - 8980 RMVar_ID_8980 Human_SNP_ID_335242695 A-to-I Human chr7 - 110432145 110432145 110432145 CACCATGCCCAGCTAATTTTTTTATTTTTAGTAGAGACATGTTTCACCATGTTGCCAAGGCTGGT CACCATGCCCAGCTAATTTTTTTATTTTTAGTTGAGACATGTTTCACCATGTTGCCAAGGCTGGT T A AC073114.1 Ensembl:ENSG00000226965 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1330850940 Functional Loss SNV dbSNP153 33..33 33 - - - 8981 RMVar_ID_8981 Human_SNP_ID_335242703 A-to-I Human chr7 - 110432199 110432199 110432199 TCAAGCAATTCTTGTGCCTCAGTCACCCAAGTAGCTAGAATTACAGTCATGCGTCACCATGCCCA TCAAGCAATTCTTGTGCCTCAGTCACCCAAGTGGCTAGAATTACAGTCATGCGTCACCATGCCCA T C AC073114.1 Ensembl:ENSG00000226965 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1440658758 Functional Loss SNV dbSNP153 33..33 33 - - - 8982 RMVar_ID_8982 Human_SNP_ID_335348618 A-to-I Human chr7 - 110861377 110861377 110861377 CTGTAGTCCCTCCTACTCGGGAGGATTACCTAAGCCTGGGGAGTTTGAGGATGCAGTGAGCCAAT CTGTAGTCCCTCCTACTCGGGAGGATTACCTACGCCTGGGGAGTTTGAGGATGCAGTGAGCCAAT T G IMMP2L Ensembl:ENSG00000184903 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1238565823 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95445,RMVar_hsa_circ_109595,RMVar_hsa_circ_247831,RMVar_hsa_circ_247832 8983 RMVar_ID_8983 Human_SNP_ID_335348652 A-to-I Human chr7 - 110861540 110861540 110861540 GTTTAAAAGGCCAGATGTGGTGGCTCACACCTATAAAACCCAGCACTTTGGGAGGCTGAGGCTGG GTTTAAAAGGCCAGATGTGGTGGCTCACACCTGTAAAACCCAGCACTTTGGGAGGCTGAGGCTGG T C IMMP2L Ensembl:ENSG00000184903 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs770331459 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95445,RMVar_hsa_circ_109595,RMVar_hsa_circ_247831,RMVar_hsa_circ_247832 8984 RMVar_ID_8984 Human_SNP_ID_335369977 A-to-I Human chr7 - 110950762 110950762 110950762 TACATCAAACTCATAGAACTCAACAGCTTTGTAAGGAACAGAGCTGGGACTGCACTTCCTGTCAT TACATCAAACTCATAGAACTCAACAGCTTTGTGAGGAACAGAGCTGGGACTGCACTTCCTGTCAT T C IMMP2L Ensembl:ENSG00000184903 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1397721982 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_68256,RMVar_hsa_circ_297778,RMVar_hsa_circ_247833 8985 RMVar_ID_8985 Human_SNP_ID_335416127 A-to-I Human chr7 - 111141993 111141993 111141993 GTATGCAAAATTGAATACTGATCTTTAGGCACAGTGGCTCATGCCTGCAATCCTAGCACTTTGGG GTATGCAAAATTGAATACTGATCTTTAGGCACGGTGGCTCATGCCTGCAATCCTAGCACTTTGGG T C IMMP2L Ensembl:ENSG00000184903 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs922533173 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 8986 RMVar_ID_8986 Human_SNP_ID_335419248 A-to-I Human chr7 - 111154833 111154833 111154833 GGATCACTTCAACCTGGGAAGTCAAGGCTGCAATGAACCATGGTCACACCACTGTACTCCGGCTT GGATCACTTCAACCTGGGAAGTCAAGGCTGCAGTGAACCATGGTCACACCACTGTACTCCGGCTT T C IMMP2L Ensembl:ENSG00000184903 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs958705399 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 8987 RMVar_ID_8987 Human_SNP_ID_335419287 A-to-I Human chr7 - 111154957 111154957 111154957 GTCCAGGAGTTCGAGACCAACCTGGGCAACATAGTGGGACCCTGTCTCTACAAAAAATTAAAAAA GTCCAGGAGTTCGAGACCAACCTGGGCAACATCGTGGGACCCTGTCTCTACAAAAAATTAAAAAA T G IMMP2L Ensembl:ENSG00000184903 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1562863783 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 8988 RMVar_ID_8988 Human_SNP_ID_335431874 A-to-I Human chr7 - 111207633 111207633 111207633 TACTCAGGAGGCTGAGGCAGTAGAATCGCTTGAACCCGGAAGGCTGAGGTTGCAGTGAGGGATTG TACTCAGGAGGCTGAGGCAGTAGAATCGCTTGGACCCGGAAGGCTGAGGTTGCAGTGAGGGATTG T C IMMP2L Ensembl:ENSG00000184903 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1373738603 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 8989 RMVar_ID_8989 Human_SNP_ID_335443960 A-to-I Human chr7 - 111258756 111258756 111258756 CACACCTATAAGCCCAGCACTTTAGGAAGTCAAGGCGGGCAGATCGCTTGAGGTCAGGAGTTTGA CACACCTATAAGCCCAGCACTTTAGGAAGTCAGGGCGGGCAGATCGCTTGAGGTCAGGAGTTTGA T C IMMP2L Ensembl:ENSG00000184903 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1394161871 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 8990 RMVar_ID_8990 Human_SNP_ID_335443962 A-to-I Human chr7 - 111258765 111258765 111258765 ACGGTGGCTCACACCTATAAGCCCAGCACTTTAGGAAGTCAAGGCGGGCAGATCGCTTGAGGTCA ACGGTGGCTCACACCTATAAGCCCAGCACTTTGGGAAGTCAAGGCGGGCAGATCGCTTGAGGTCA T C IMMP2L Ensembl:ENSG00000184903 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs774654171 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 8991 RMVar_ID_8991 Human_SNP_ID_335443965 A-to-I Human chr7 - 111258781 111258781 111258781 GTTTTTCTGGCTAGGCACGGTGGCTCACACCTATAAGCCCAGCACTTTAGGAAGTCAAGGCGGGC GTTTTTCTGGCTAGGCACGGTGGCTCACACCTGTAAGCCCAGCACTTTAGGAAGTCAAGGCGGGC T C IMMP2L Ensembl:ENSG00000184903 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs929594140 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 8992 RMVar_ID_8992 Human_SNP_ID_335443966 A-to-I Human chr7 - 111258781 111258781 111258781 GTTTTTCTGGCTAGGCACGGTGGCTCACACCTATAAGCCCAGCACTTTAGGAAGTCAAGGCGGGC GTTTTTCTGGCTAGGCACGGTGGCTCACACCTCTAAGCCCAGCACTTTAGGAAGTCAAGGCGGGC T G IMMP2L Ensembl:ENSG00000184903 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs929594140 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 8993 RMVar_ID_8993 Human_SNP_ID_335443977 A-to-I Human chr7 - 111258801 111258801 111258801 CATATTTATTTCAAAAATATGTTTTTCTGGCTAGGCACGGTGGCTCACACCTATAAGCCCAGCAC CATATTTATTTCAAAAATATGTTTTTCTGGCTTGGCACGGTGGCTCACACCTATAAGCCCAGCAC T A IMMP2L Ensembl:ENSG00000184903 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256894983 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 8994 RMVar_ID_8994 Human_SNP_ID_335443978 A-to-I Human chr7 - 111258801 111258801 111258801 CATATTTATTTCAAAAATATGTTTTTCTGGCTAGGCACGGTGGCTCACACCTATAAGCCCAGCAC CATATTTATTTCAAAAATATGTTTTTCTGGCTGGGCACGGTGGCTCACACCTATAAGCCCAGCAC T C IMMP2L Ensembl:ENSG00000184903 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256894983 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 8995 RMVar_ID_8995 Human_SNP_ID_335449352 A-to-I Human chr7 - 111280813 111280813 111280813 TGCCTGCCTCGGCCTCCCAAAGTCCTGGGATTACAGGCCTGAGCCACCGCACCCGGCCAATTTCA TGCCTGCCTCGGCCTCCCAAAGTCCTGGGATTGCAGGCCTGAGCCACCGCACCCGGCCAATTTCA T C IMMP2L Ensembl:ENSG00000184903 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs925655597 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 8996 RMVar_ID_8996 Human_SNP_ID_335462925 A-to-I Human chr7 - 111334388 111334388 111334388 TATTATTCTGCCATAAAAAAGAATGAAATCCTATCATGTACAGCAACGTGGATGAAACAGAAGGC TATTATTCTGCCATAAAAAAGAATGAAATCCTGTCATGTACAGCAACGTGGATGAAACAGAAGGC T C IMMP2L Ensembl:ENSG00000184903 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1372401241 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3043883 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 8997 RMVar_ID_8997 Human_SNP_ID_335462939 A-to-I Human chr7 - 111334451 111334451 111334451 CAACCTAAGTGCCAATCAACTGATGCATGCATAAAGAAAATGTGGTATATATACCCAGTGGAATA CAACCTAAGTGCCAATCAACTGATGCATGCATGAAGAAAATGTGGTATATATACCCAGTGGAATA T C IMMP2L Ensembl:ENSG00000184903 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1480096148 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 8998 RMVar_ID_8998 Human_SNP_ID_335468283 A-to-I Human chr7 - 111356870 111356870 111356870 GGCACCCACCACAACGCCTGGCTAATTTTTGTATTTTTAGTGGAGATAGGGTTTCACCGTGTTGG GGCACCCACCACAACGCCTGGCTAATTTTTGTGTTTTTAGTGGAGATAGGGTTTCACCGTGTTGG T C IMMP2L Ensembl:ENSG00000184903 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs548961716 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26060604 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 8999 RMVar_ID_8999 Human_SNP_ID_335478966 A-to-I Human chr7 - 111402545 111402545 111402545 TACTGCGCCTGGCTAATTTTCGTATTTTTATTAGAGACGGGGTTTCACTGTGTTGCCTGGGCTGG TACTGCGCCTGGCTAATTTTCGTATTTTTATTCGAGACGGGGTTTCACTGTGTTGCCTGGGCTGG T G IMMP2L Ensembl:ENSG00000184903 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973045489 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3045087,Human_RBP_ID_15976979,Human_RBP_ID_26060973 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 9000 RMVar_ID_9000 Human_SNP_ID_335494924 A-to-I Human chr7 + 111465156 111465156 111465156 GTAAACTACCCATTGTCCAAAAGATCAGTAACACCTGTCACTCCTGCCATAATGGGCTCTCTGAC GTAAACTACCCATTGTCCAAAAGATCAGTAACCCCTGTCACTCCTGCCATAATGGGCTCTCTGAC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1043818957 Functional Loss SNV dbSNP153 33..33 33 - - - 9001 RMVar_ID_9001 Human_SNP_ID_335654608 A-to-I Human chr7 - 112105724 112105724 112105724 TAATTGCATCACTGCACTCCAGCCTAGGTGACAGACTGAGACGCTGCCTCGAAGAAAAAAAAAAA TAATTGCATCACTGCACTCCAGCCTAGGTGACGGACTGAGACGCTGCCTCGAAGAAAAAAAAAAA T C DOCK4 Ensembl:ENSG00000128512 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs551650454 Functional Loss SNV dbSNP153 33..33 33 - - - 9002 RMVar_ID_9002 Human_SNP_ID_335656187 A-to-I Human chr7 - 112112528 112112528 112112528 GTGATTCTCCTGCCTCAGCCTCCTGAGTAGGTAGGACTACAGGTGCCCACCACCACACCCGGCTA GTGATTCTCCTGCCTCAGCCTCCTGAGTAGGTGGGACTACAGGTGCCCACCACCACACCCGGCTA T C DOCK4 Ensembl:ENSG00000128512 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs753172040 Functional Loss SNV dbSNP153 33..33 33 - - - 9003 RMVar_ID_9003 Human_SNP_ID_335700749 A-to-I Human chr7 + 112305159 112305159 112305159 CATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGAGAGAATCGCTTGAACTCAGGAGACCAG CATGCCTGTAATCCCAGCACTTTGGGAGGCTGTGGCGAGAGAATCGCTTGAACTCAGGAGACCAG A T ZNF277 Ensembl:ENSG00000198839 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs538301409 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_65087,RMVar_hsa_circ_69856,RMVar_hsa_circ_368790,RMVar_hsa_circ_247890,RMVar_hsa_circ_274219,RMVar_hsa_circ_321274,RMVar_hsa_circ_53538,RMVar_hsa_circ_247894,RMVar_hsa_circ_28209,RMVar_hsa_circ_247893 9004 RMVar_ID_9004 Human_SNP_ID_335734702 A-to-I Human chr7 + 112455467 112455467 112455467 AGATTGTGCCACTGCACTGCAGCCAGGGCGACAGGGAGGCTCTGTCTCAAAAAAACAAAAAAAAC AGATTGTGCCACTGCACTGCAGCCAGGGCGACTGGGAGGCTCTGTCTCAAAAAAACAAAAAAAAC A T IFRD1 Ensembl:ENSG00000006652 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1010645553 Functional Loss SNV dbSNP153 33..33 33 - - - 9005 RMVar_ID_9005 Human_SNP_ID_335735647 A-to-I Human chr7 + 112459084 112459081 112459084 CTATTCATGACACCCAGACGTGGTGCGCCTATAGTACTGTACCAGCTACTCAAGAGGCTGAGGCA CTATTCATGACACCCAGACGTGGTGCGCCT___GTACTGTACCAGCTACTCAAGAGGCTGAGGCA TATA T IFRD1 Ensembl:ENSG00000006652 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs34627083 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_2033604,Human_RBP_ID_5401730,Human_RBP_ID_7679844,Human_RBP_ID_8655345,Human_RBP_ID_9202942,Human_RBP_ID_15980464,Human_RBP_ID_19135409,Human_RBP_ID_23071282,Human_RBP_ID_24185020,Human_RBP_ID_24439108 RMVar_hsa_circ_356265,RMVar_hsa_circ_73632,RMVar_hsa_circ_27099,RMVar_hsa_circ_293152,RMVar_hsa_circ_328955,RMVar_hsa_circ_319513,RMVar_hsa_circ_336632,RMVar_hsa_circ_98013,RMVar_hsa_circ_32324,RMVar_hsa_circ_247898,RMVar_hsa_circ_247900,RMVar_hsa_circ_247899 9006 RMVar_ID_9006 Human_SNP_ID_335735651 A-to-I Human chr7 + 112459084 112459083 112459084 CTATTCATGACACCCAGACGTGGTGCGCCTATAGTACTGTACCAGCTACTCAAGAGGCTGAGGCA CTATTCATGACACCCAGACGTGGTGCGCCTAT_GTACTGTACCAGCTACTCAAGAGGCTGAGGCA TA T IFRD1 Ensembl:ENSG00000006652 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1554507581 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_2033604,Human_RBP_ID_5401730,Human_RBP_ID_7679844,Human_RBP_ID_8655345,Human_RBP_ID_9202942,Human_RBP_ID_15980464,Human_RBP_ID_19135409,Human_RBP_ID_23071282,Human_RBP_ID_24185020,Human_RBP_ID_24439108 RMVar_hsa_circ_356265,RMVar_hsa_circ_73632,RMVar_hsa_circ_27099,RMVar_hsa_circ_293152,RMVar_hsa_circ_328955,RMVar_hsa_circ_319513,RMVar_hsa_circ_336632,RMVar_hsa_circ_98013,RMVar_hsa_circ_32324,RMVar_hsa_circ_247898,RMVar_hsa_circ_247900,RMVar_hsa_circ_247899 9007 RMVar_ID_9007 Human_SNP_ID_335735652 A-to-I Human chr7 + 112459084 112459084 112459084 CTATTCATGACACCCAGACGTGGTGCGCCTATAGTACTGTACCAGCTACTCAAGAGGCTGAGGCA CTATTCATGACACCCAGACGTGGTGCGCCTATTGTACTGTACCAGCTACTCAAGAGGCTGAGGCA A T IFRD1 Ensembl:ENSG00000006652 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1372420240 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2033604,Human_RBP_ID_5401730,Human_RBP_ID_7679844,Human_RBP_ID_8655345,Human_RBP_ID_9202942,Human_RBP_ID_15980464,Human_RBP_ID_19135409,Human_RBP_ID_23071282,Human_RBP_ID_24185020,Human_RBP_ID_24439108 RMVar_hsa_circ_356265,RMVar_hsa_circ_73632,RMVar_hsa_circ_27099,RMVar_hsa_circ_293152,RMVar_hsa_circ_328955,RMVar_hsa_circ_319513,RMVar_hsa_circ_336632,RMVar_hsa_circ_98013,RMVar_hsa_circ_32324,RMVar_hsa_circ_247898,RMVar_hsa_circ_247900,RMVar_hsa_circ_247899 9008 RMVar_ID_9008 Human_SNP_ID_335799786 A-to-I Human chr7 - 112735250 112735250 112735250 AAGCCCATGCTCATGGTTGAAGGTGTGCTTCAAAAGTGCCCTTCTATTGATTACTTTGTAAGTGC AAGCCCATGCTCATGGTTGAAGGTGTGCTTCAGAAGTGCCCTTCTATTGATTACTTTGTAAGTGC T C MIPEPP1 Ensembl:ENSG00000225358 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1300566608 Functional Loss SNV dbSNP153 33..33 33 - - - 9009 RMVar_ID_9009 Human_SNP_ID_336218171 A-to-I Human chr7 + 114462150 114462150 114462150 TAAAAATACAAAAATTAGCCGGGCGCGGTGGCACGTGCCTGTAGTCCCAGCTACTCGGGAGGCTG TAAAAATACAAAAATTAGCCGGGCGCGGTGGCGCGTGCCTGTAGTCCCAGCTACTCGGGAGGCTG A G FOXP2 Ensembl:ENSG00000128573 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1336773751 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_176968 RMVar_hsa_circ_2389,RMVar_hsa_circ_39176,RMVar_hsa_circ_67869,RMVar_hsa_circ_14126,RMVar_hsa_circ_279013,RMVar_hsa_circ_328704,RMVar_hsa_circ_304640 9010 RMVar_ID_9010 Human_SNP_ID_336726583 A-to-I Human chr7 + 116507692 116507683 116507692 AGAGTCTGTCTCAAAAAAAAAAAGAAAAAAAGAAAAAAAGAAAAAAGAAAAATCTCATTATTTCA AGAGTCTGTCTCAAAAAAAAAAAG_________AAAAAAGAAAAAAGAAAAATCTCATTATTTCA GAAAAAAAGA G CAV2 Ensembl:ENSG00000105971 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs767919217 Functional Loss DEL dbSNP153 25..33 33 - - - 9011 RMVar_ID_9011 Human_SNP_ID_336726584 A-to-I Human chr7 + 116507684 116507683 116507685 ACAGAGCAAGAGTCTGTCTCAAAAAAAAAAAGAAAAAAAGAAAAAAAGAAAAAAGAAAAATCTCA ACAGAGCAAGAGTCTGTCTCAAAAAAAAAAAG__AAAAAGAAAAAAAGAAAAAAGAAAAATCTCA GAA G CAV2 Ensembl:ENSG00000105971 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs778056588 Functional Loss DEL dbSNP153 33..34 33 - - - 9012 RMVar_ID_9012 Human_SNP_ID_336726585 A-to-I Human chr7 + 116507684 116507684 116507684 ACAGAGCAAGAGTCTGTCTCAAAAAAAAAAAGAAAAAAAGAAAAAAAGAAAAAAGAAAAATCTCA ACAGAGCAAGAGTCTGTCTCAAAAAAAAAAAGCAAAAAAGAAAAAAAGAAAAAAGAAAAATCTCA A C CAV2 Ensembl:ENSG00000105971 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1487388319 Functional Loss SNV dbSNP153 33..33 33 - - - 9013 RMVar_ID_9013 Human_SNP_ID_336726591 A-to-I Human chr7 + 116507692 116507691 116507692 AGAGTCTGTCTCAAAAAAAAAAAGAAAAAAAGAAAAAAAGAAAAAAGAAAAATCTCATTATTTCA AGAGTCTGTCTCAAAAAAAAAAAGAAAAAAAG_AAAAAAGAAAAAAGAAAAATCTCATTATTTCA GA G CAV2 Ensembl:ENSG00000105971 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1230375285 Functional Loss DEL dbSNP153 33..33 33 - - - 9014 RMVar_ID_9014 Human_SNP_ID_336838384 A-to-I Human chr7 + 116966344 116966344 116966344 ATGATCTTGGCTCACTGCAACCTCCACCTTCCAGGTTGAAGTGATTCTCGGGCTTCAGCCTCCTG ATGATCTTGGCTCACTGCAACCTCCACCTTCCGGGTTGAAGTGATTCTCGGGCTTCAGCCTCCTG A G ST7,ST7-OT4 Ensembl:ENSG00000004866,Ensembl:ENSG00000214188 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs902244570 Functional Loss SNV dbSNP153 33..33 33 - - - 9015 RMVar_ID_9015 Human_SNP_ID_336838394 A-to-I Human chr7 + 116966390 116966390 116966390 CTCGGGCTTCAGCCTCCTGAGTAGTTGGGATTACAGGCACCTGCCACCACACCTGGCTAATTTTT CTCGGGCTTCAGCCTCCTGAGTAGTTGGGATTGCAGGCACCTGCCACCACACCTGGCTAATTTTT A G ST7,ST7-OT4 Ensembl:ENSG00000004866,Ensembl:ENSG00000214188 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560700363 Functional Loss SNV dbSNP153 33..33 33 - - - 9016 RMVar_ID_9016 Human_SNP_ID_336868562 A-to-I Human chr7 + 117103691 117103691 117103691 TGGGGAAATGCTCCAGAACATTAGTCTGGGTAAAGACTTTTTGTGTGAGACCTCAAAGCACAGGC TGGGGAAATGCTCCAGAACATTAGTCTGGGTAGAGACTTTTTGTGTGAGACCTCAAAGCACAGGC A G ST7 Ensembl:ENSG00000004866 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs958703918 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_247950,RMVar_hsa_circ_342285,RMVar_hsa_circ_364018,RMVar_hsa_circ_66552,RMVar_hsa_circ_311124,RMVar_hsa_circ_44742,RMVar_hsa_circ_278934,RMVar_hsa_circ_300631,RMVar_hsa_circ_357421,RMVar_hsa_circ_247949,RMVar_hsa_circ_360605,RMVar_hsa_circ_314226,RMVar_hsa_circ_284401,RMVar_hsa_circ_247952,RMVar_hsa_circ_247953,RMVar_hsa_circ_247951 9017 RMVar_ID_9017 Human_SNP_ID_336872623 A-to-I Human chr7 + 117122273 117122273 117122273 TTGTGACAGAAGCCAAAGTTGCCAAGTAGCTCATGCTGTGCTAAGGAATCTGGAACCTGGGCCTT TTGTGACAGAAGCCAAAGTTGCCAAGTAGCTCGTGCTGTGCTAAGGAATCTGGAACCTGGGCCTT A G ST7 Ensembl:ENSG00000004866 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1243667527 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_247950,RMVar_hsa_circ_342285,RMVar_hsa_circ_364018,RMVar_hsa_circ_66552,RMVar_hsa_circ_311124,RMVar_hsa_circ_278934,RMVar_hsa_circ_300631,RMVar_hsa_circ_357421,RMVar_hsa_circ_247949,RMVar_hsa_circ_360605,RMVar_hsa_circ_284401,RMVar_hsa_circ_337903,RMVar_hsa_circ_247952,RMVar_hsa_circ_247953,RMVar_hsa_circ_365640,RMVar_hsa_circ_247951,RMVar_hsa_circ_344997 9018 RMVar_ID_9018 Human_SNP_ID_337022615 A-to-I Human chr7 - 117789897 117789897 117789897 AGAGGCTTTATCCATATTTTGAGGGGCGAAATAGGGAATTGGAAGCAGCATGGACTTGGAAGTTA AGAGGCTTTATCCATATTTTGAGGGGCGAAATTGGGAATTGGAAGCAGCATGGACTTGGAAGTTA T A CTTNBP2 Ensembl:ENSG00000077063 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1397224081 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86232,RMVar_hsa_circ_247973,RMVar_hsa_circ_247981,RMVar_hsa_circ_95617 9019 RMVar_ID_9019 Human_SNP_ID_4054644 A-to-I Human chr1 + 15041602 15041602 15041602 CAGGTGATCCATCCACCTCAGCCTCCCAAAATACTGGGACTACAGGCATGAGCCACTGTGCCCGG CAGGTGATCCATCCACCTCAGCCTCCCAAAATTCTGGGACTACAGGCATGAGCCACTGTGCCCGG A T KAZN Ensembl:ENSG00000189337 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs767827036 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267660,RMVar_hsa_circ_129379,RMVar_hsa_circ_289103 9020 RMVar_ID_9020 Human_SNP_ID_4169773 A-to-I Human chr1 - 15490012 15490012 15490012 AAAATTAGTTGGGCATGGTGGTGCATGCCTGTAATCCCAGCTAGTTAGGAGGCTGAGGCAGGAGA AAAATTAGTTGGGCATGGTGGTGCATGCCTGTGATCCCAGCTAGTTAGGAGGCTGAGGCAGGAGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1464029808 Functional Loss SNV dbSNP153 33..33 33 - - - 9021 RMVar_ID_9021 Human_SNP_ID_4169955 A-to-I Human chr1 - 15490623 15490623 15490623 CCTCAAGTGATCTACCCGTCTCGGCTTCCCAAAGTGCTCGGATTACAGGCGTGAGCCACCGCGCC CCTCAAGTGATCTACCCGTCTCGGCTTCCCAATGTGCTCGGATTACAGGCGTGAGCCACCGCGCC T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1557528562 Functional Loss SNV dbSNP153 33..33 33 - - - 9022 RMVar_ID_9022 Human_SNP_ID_4169964 A-to-I Human chr1 - 15490650 15490650 15490650 TTGGCCAGGCTGGTCTCGAACTGCTGACCTCAAGTGATCTACCCGTCTCGGCTTCCCAAAGTGCT TTGGCCAGGCTGGTCTCGAACTGCTGACCTCAGGTGATCTACCCGTCTCGGCTTCCCAAAGTGCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs925634913 Functional Loss SNV dbSNP153 33..33 33 - - - 9023 RMVar_ID_9023 Human_SNP_ID_4170234 A-to-I Human chr1 - 15491675 15491674 15491676 TGGCTTATTGCAGTCTCGACCTCCTGGGCTCAAGAGATCCTTCCACCTCAGCCACCTGAGTAGCT TGGCTTATTGCAGTCTCGACCTCCTGGGCTC__GAGATCCTTCCACCTCAGCCACCTGAGTAGCT CTT C CASP9 Ensembl:ENSG00000132906 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054037901 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_79340,RMVar_hsa_circ_129389 9024 RMVar_ID_9024 Human_SNP_ID_4175913 A-to-I Human chr1 - 15513742 15513742 15513742 AGAACAAATGGCTCATTCTCTTTCTTGTCCCTATATTTGTGCCATTACTCATTAGCTCACACAAA AGAACAAATGGCTCATTCTCTTTCTTGTCCCTGTATTTGTGCCATTACTCATTAGCTCACACAAA T C CASP9 Ensembl:ENSG00000132906 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs745690533 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79340,RMVar_hsa_circ_129389,RMVar_hsa_circ_338203,RMVar_hsa_circ_61453 9025 RMVar_ID_9025 Human_SNP_ID_4175914 A-to-I Human chr1 - 15513742 15513742 15513742 AGAACAAATGGCTCATTCTCTTTCTTGTCCCTATATTTGTGCCATTACTCATTAGCTCACACAAA AGAACAAATGGCTCATTCTCTTTCTTGTCCCTCTATTTGTGCCATTACTCATTAGCTCACACAAA T G CASP9 Ensembl:ENSG00000132906 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs745690533 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79340,RMVar_hsa_circ_129389,RMVar_hsa_circ_338203,RMVar_hsa_circ_61453 9026 RMVar_ID_9026 Human_SNP_ID_4191190 A-to-I Human chr1 - 15571982 15571982 15571982 CGTCACCACGCCCGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGC CGTCACCACGCCCGGCTAATTTTTGTATTTTTGGTAGAGACGGGGTTTCACCATGTTGGCCAGGC T C AGMAT Ensembl:ENSG00000116771 Protein coding 3'UTR GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs1168906006 Functional Loss SNV dbSNP153 33..33 33 - - - 9027 RMVar_ID_9027 Human_SNP_ID_4191206 A-to-I Human chr1 - 15572021 15572020 15572022 GCTGCCTCAGCCTCCTGAGTAGCTAGAATTACAGTCATGCGTCACCACGCCCGGCTAATTTTTGT GCTGCCTCAGCCTCCTGAGTAGCTAGAATTA__GTCATGCGTCACCACGCCCGGCTAATTTTTGT CTG C AGMAT Ensembl:ENSG00000116771 Protein coding 3'UTR GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1216748091 Functional Loss DEL dbSNP153 32..33 33 - - - 9028 RMVar_ID_9028 Human_SNP_ID_4191214 A-to-I Human chr1 - 15572093 15572093 15572093 TCCCCCAGGCTGGAGTGCAGTGGCCCGATCTTAGCTCACTGCAATCTCCGCCTCCTGGGTTCAAG TCCCCCAGGCTGGAGTGCAGTGGCCCGATCTTCGCTCACTGCAATCTCCGCCTCCTGGGTTCAAG T G AGMAT Ensembl:ENSG00000116771 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1202231953 Functional Loss SNV dbSNP153 33..33 33 - - - 9029 RMVar_ID_9029 Human_SNP_ID_4191291 A-to-I Human chr1 - 15572262 15572262 15572262 GAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAAACAAAA GAGGTCAGGAGTTCAAGACCAGCCTGGCCAACGTGGTGAAACCCCGTCTCTACTAAAAAACAAAA T C AGMAT Ensembl:ENSG00000116771 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1392387419 Functional Loss SNV dbSNP153 33..33 33 - - - 9030 RMVar_ID_9030 Human_SNP_ID_4191364 A-to-I Human chr1 - 15572414 15572414 15572414 TGGAGGTTGCAGTGAGCTGAGGTCATGCCACTACACTCCAGCCTGGGTGACAGAGTGAGACTCCG TGGAGGTTGCAGTGAGCTGAGGTCATGCCACTGCACTCCAGCCTGGGTGACAGAGTGAGACTCCG T C AGMAT Ensembl:ENSG00000116771 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs560327297 Functional Loss SNV dbSNP153 33..33 33 - - - 9031 RMVar_ID_9031 Human_SNP_ID_4191378 A-to-I Human chr1 - 15572480 15572480 15572480 TGGCGCGTGCCTATAGTCCCAGCTACTCAGGAAGCTGAGGCAGGGGCATTGCTTGAACCCGGGAG TGGCGCGTGCCTATAGTCCCAGCTACTCAGGAGGCTGAGGCAGGGGCATTGCTTGAACCCGGGAG T C AGMAT Ensembl:ENSG00000116771 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1053221687 Functional Loss SNV dbSNP153 33..33 33 - - - 9032 RMVar_ID_9032 Human_SNP_ID_4191380 A-to-I Human chr1 - 15572500 15572500 15572500 CAGAAGTTAGCTGGGCGTGGTGGCGCGTGCCTATAGTCCCAGCTACTCAGGAAGCTGAGGCAGGG CAGAAGTTAGCTGGGCGTGGTGGCGCGTGCCTTTAGTCCCAGCTACTCAGGAAGCTGAGGCAGGG T A AGMAT Ensembl:ENSG00000116771 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1246956434 Functional Loss SNV dbSNP153 33..33 33 - - - 9033 RMVar_ID_9033 Human_SNP_ID_4191381 A-to-I Human chr1 - 15572500 15572500 15572500 CAGAAGTTAGCTGGGCGTGGTGGCGCGTGCCTATAGTCCCAGCTACTCAGGAAGCTGAGGCAGGG CAGAAGTTAGCTGGGCGTGGTGGCGCGTGCCTGTAGTCCCAGCTACTCAGGAAGCTGAGGCAGGG T C AGMAT Ensembl:ENSG00000116771 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1246956434 Functional Loss SNV dbSNP153 33..33 33 - - - 9034 RMVar_ID_9034 Human_SNP_ID_4191397 A-to-I Human chr1 - 15572542 15572542 15572542 CAGCCTGGCCAACATGGTGAAAACCCATCTCTACTGAAAATACAGAAGTTAGCTGGGCGTGGTGG CAGCCTGGCCAACATGGTGAAAACCCATCTCTGCTGAAAATACAGAAGTTAGCTGGGCGTGGTGG T C AGMAT Ensembl:ENSG00000116771 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1024847609 Functional Loss SNV dbSNP153 33..33 33 - - - 9035 RMVar_ID_9035 Human_SNP_ID_4191411 A-to-I Human chr1 - 15572602 15572602 15572602 TAATCCCAGCACTTTGGGGGGCGGAGGTGGGCAGATCACTTGAGGTCAGGAGTTCGAGACCAGCC TAATCCCAGCACTTTGGGGGGCGGAGGTGGGCTGATCACTTGAGGTCAGGAGTTCGAGACCAGCC T A AGMAT Ensembl:ENSG00000116771 Protein coding 3'UTR GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs952595815 Functional Loss SNV dbSNP153 33..33 33 - - - 9036 RMVar_ID_9036 Human_SNP_ID_4191500 A-to-I Human chr1 - 15572892 15572892 15572892 TAAACTACAGCTCCTCCTCGGACGCTGCAGTGAGCTGAGATCGCACCACTGCACTCCAGCCTGGG TAAACTACAGCTCCTCCTCGGACGCTGCAGTGGGCTGAGATCGCACCACTGCACTCCAGCCTGGG T C AGMAT Ensembl:ENSG00000116771 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line - 23474544,24183664,29129909,32596459 RNA-Seq:(High) rs1025936255 Functional Loss SNV dbSNP153 33..33 33 - - - 9037 RMVar_ID_9037 Human_SNP_ID_4191578 A-to-I Human chr1 - 15573215 15573215 15573215 TTTGCTTGTCACCCAGGCTGGAGTGCAATGGCATGATCTCGGTTCATTGCAACCTCCGCCTCCCG TTTGCTTGTCACCCAGGCTGGAGTGCAATGGCGTGATCTCGGTTCATTGCAACCTCCGCCTCCCG T C AGMAT Ensembl:ENSG00000116771 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs912912179 Functional Loss SNV dbSNP153 33..33 33 - - - 9038 RMVar_ID_9038 Human_SNP_ID_4195916 A-to-I Human chr1 + 15587696 15587696 15587696 TCATGAAGGCTGTGGTGCTGTGGTACAGTCATAGCTCACTGCAGCCTCCACCCCCTGGGCTTGAG TCATGAAGGCTGTGGTGCTGTGGTACAGTCATGGCTCACTGCAGCCTCCACCCCCTGGGCTTGAG A G DNAJC16 Ensembl:ENSG00000116138 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1158182980 Functional Loss SNV dbSNP153 33..33 33 - - - 9039 RMVar_ID_9039 Human_SNP_ID_4208600 A-to-I Human chr1 + 15635585 15635585 15635585 GTACCACCACGCCCGGCTATTTTGGTATTTTTAGTAAAGATGGGGTTTCACCATCTTGGCCAGGC GTACCACCACGCCCGGCTATTTTGGTATTTTTGGTAAAGATGGGGTTTCACCATCTTGGCCAGGC A G DDI2 Ensembl:ENSG00000197312 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs767058256 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5974,RMVar_hsa_circ_129415,RMVar_hsa_circ_272185,RMVar_hsa_circ_315790,RMVar_hsa_circ_275857,RMVar_hsa_circ_54175,RMVar_hsa_circ_81556,RMVar_hsa_circ_129416,RMVar_hsa_circ_129417,RMVar_hsa_circ_129419,RMVar_hsa_circ_278059,RMVar_hsa_circ_335912,RMVar_hsa_circ_346466,RMVar_hsa_circ_317250,RMVar_hsa_circ_275965,RMVar_hsa_circ_372213,RMVar_hsa_circ_129418,RMVar_hsa_circ_40526,RMVar_hsa_circ_129422,RMVar_hsa_circ_129421,RMVar_hsa_circ_77066 9040 RMVar_ID_9040 Human_SNP_ID_4212853 A-to-I Human chr1 + 15652178 15652178 15652178 TTCACTGCACCCTTGACTTCCTGGGCTCAAGCAGTCCTCTCACCTCAGCCTCCTGAGTAGCTGGG TTCACTGCACCCTTGACTTCCTGGGCTCAAGCGGTCCTCTCACCTCAGCCTCCTGAGTAGCTGGG A G DDI2 Ensembl:ENSG00000197312 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910273807 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54175,RMVar_hsa_circ_335912,RMVar_hsa_circ_344695,RMVar_hsa_circ_129423 9041 RMVar_ID_9041 Human_SNP_ID_4213350 A-to-I Human chr1 + 15653575 15653575 15653575 ACTTAATTAAAAAAAAAATTTTTTTTTGAGACAAGGTCTTACTCTGTCACCCAGACTGATCCTCC ACTTAATTAAAAAAAAAATTTTTTTTTGAGACCAGGTCTTACTCTGTCACCCAGACTGATCCTCC A C DDI2 Ensembl:ENSG00000197312 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs948010623 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54175,RMVar_hsa_circ_335912,RMVar_hsa_circ_344695,RMVar_hsa_circ_129423 9042 RMVar_ID_9042 Human_SNP_ID_4216855 A-to-I Human chr1 - 15667203 15667203 15667203 TTCCATTTAAAAAAAAATTTTTTTTTTTTTTGAGACGGTGTCTCACTCTTGCCCAGGCTGGAGTA TTCCATTTAAAAAAAAATTTTTTTTTTTTTTGTGACGGTGTCTCACTCTTGCCCAGGCTGGAGTA T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1431886225 Functional Loss SNV dbSNP153 33..33 33 - - - 9043 RMVar_ID_9043 Human_SNP_ID_4216856 A-to-I Human chr1 - 15667203 15667203 15667203 TTCCATTTAAAAAAAAATTTTTTTTTTTTTTGAGACGGTGTCTCACTCTTGCCCAGGCTGGAGTA TTCCATTTAAAAAAAAATTTTTTTTTTTTTTGGGACGGTGTCTCACTCTTGCCCAGGCTGGAGTA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1431886225 Functional Loss SNV dbSNP153 33..33 33 - - - 9044 RMVar_ID_9044 Human_SNP_ID_4222478 A-to-I Human chr1 + 15689078 15689078 15689078 CGAGACCGGCCTGACCAACATCGAGAAACCCCATCTCTATTAAAAATACAAAATTAGCTAGGTGT CGAGACCGGCCTGACCAACATCGAGAAACCCCGTCTCTATTAAAAATACAAAATTAGCTAGGTGT A G PLEKHM2 Ensembl:ENSG00000116786 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968510504 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_129433,RMVar_hsa_circ_91755,RMVar_hsa_circ_95551,RMVar_hsa_circ_129434 9045 RMVar_ID_9045 Human_SNP_ID_4225043 A-to-I Human chr1 + 15699857 15699857 15699857 GGAGAGTAGGCTGGGCATGGTGGTGTGCGCCTATAGTCCCAGCTACATGGAAGGCTGAGGTGGAA GGAGAGTAGGCTGGGCATGGTGGTGTGCGCCTGTAGTCCCAGCTACATGGAAGGCTGAGGTGGAA A G PLEKHM2 Ensembl:ENSG00000116786 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs923827864 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_129433,RMVar_hsa_circ_91755,RMVar_hsa_circ_95551,RMVar_hsa_circ_129434 9046 RMVar_ID_9046 Human_SNP_ID_4254838 A-to-I Human chr1 - 15807417 15807417 15807417 CACGGAGGAGCTCTTTGACTTCTTGCATGCAAAGGACCATTGCGTGGCCCACAAACTCTTTAACA CACGGAGGAGCTCTTTGACTTCTTGCATGCAAGGGACCATTGCGTGGCCCACAAACTCTTTAACA T C UQCRHL Ensembl:ENSG00000233954 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs570054582 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4083642 9047 RMVar_ID_9047 Human_SNP_ID_4254839 A-to-I Human chr1 - 15807419 15807419 15807419 TGCACGGAGGAGCTCTTTGACTTCTTGCATGCAAAGGACCATTGCGTGGCCCACAAACTCTTTAA TGCACGGAGGAGCTCTTTGACTTCTTGCATGCGAAGGACCATTGCGTGGCCCACAAACTCTTTAA T C UQCRHL Ensembl:ENSG00000233954 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs10722 Functional Loss SNV dbSNP153 33..33 33 - - - 9048 RMVar_ID_9048 Human_SNP_ID_4254840 A-to-I Human chr1 - 15807419 15807419 15807419 TGCACGGAGGAGCTCTTTGACTTCTTGCATGCAAAGGACCATTGCGTGGCCCACAAACTCTTTAA TGCACGGAGGAGCTCTTTGACTTCTTGCATGCCAAGGACCATTGCGTGGCCCACAAACTCTTTAA T G UQCRHL Ensembl:ENSG00000233954 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs10722 Functional Loss SNV dbSNP153 33..33 33 - - - 9049 RMVar_ID_9049 Human_SNP_ID_4255062 A-to-I Human chr1 - 15808135 15808135 15808135 TCTCTCTGTCACCCAGACTGGAGTACAGTGACATGATCTCTGCTCACTGTGATCTCTGCCTCCCA TCTCTCTGTCACCCAGACTGGAGTACAGTGACGTGATCTCTGCTCACTGTGATCTCTGCCTCCCA T C UQCRHL Ensembl:ENSG00000233954 Protein coding 5'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1038194601 Functional Loss SNV dbSNP153 33..33 33 - - - 9050 RMVar_ID_9050 Human_SNP_ID_4257992 A-to-I Human chr1 - 15819785 15819785 15819785 TCGCCAGCGCTGGAGTGCAGTGGCGTGATCTCAGCTCACTGCAACCTCCACCTCCCGGATTCAAA TCGCCAGCGCTGGAGTGCAGTGGCGTGATCTCGGCTCACTGCAACCTCCACCTCCCGGATTCAAA T C FLJ37453 RNACentral:URS00009AF023 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474727073 Functional Loss SNV dbSNP153 33..33 33 - - - 9051 RMVar_ID_9051 Human_SNP_ID_4259503 A-to-I Human chr1 - 15825111 15825111 15825111 ATTAAGGTTGGTCGCGGTGGCTCATGCCTGTAATCCTAGCACTTTGGGAGGCTGAGGCAGGCAGA ATTAAGGTTGGTCGCGGTGGCTCATGCCTGTAGTCCTAGCACTTTGGGAGGCTGAGGCAGGCAGA T C FLJ37453 RNACentral:URS00009AF023 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1435747849 Functional Loss SNV dbSNP153 33..33 33 - - - 9052 RMVar_ID_9052 Human_SNP_ID_4260306 A-to-I Human chr1 - 15828362 15828362 15828362 CTGGCTCCAGCAGCTTGTATTGTAGCATGCGCAGCTCAATCATCTCCAGGGGCCACCCGTTCACC CTGGCTCCAGCAGCTTGTATTGTAGCATGCGCGGCTCAATCATCTCCAGGGGCCACCCGTTCACC T C FLJ37453 RNACentral:URS00009AF023 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878863606 Functional Loss SNV dbSNP153 33..33 33 - - - 9053 RMVar_ID_9053 Human_SNP_ID_4260309 A-to-I Human chr1 - 15828368 15828368 15828368 GCAGAACTGGCTCCAGCAGCTTGTATTGTAGCATGCGCAGCTCAATCATCTCCAGGGGCCACCCG GCAGAACTGGCTCCAGCAGCTTGTATTGTAGCGTGCGCAGCTCAATCATCTCCAGGGGCCACCCG T C FLJ37453 RNACentral:URS00009AF023 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879184857 Functional Loss SNV dbSNP153 33..33 33 - - - 9054 RMVar_ID_9054 Human_SNP_ID_4271165 A-to-I Human chr1 + 15863127 15863127 15863127 TAAAAGGTAGTTGGGCATGGTGGTATGTACCTATAGTCCAGCTACTTGGAAGGCTTAGGCGGGCA TAAAAGGTAGTTGGGCATGGTGGTATGTACCTGTAGTCCAGCTACTTGGAAGGCTTAGGCGGGCA A G SPEN Ensembl:ENSG00000065526 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048072190 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96122,RMVar_hsa_circ_129481 9055 RMVar_ID_9055 Human_SNP_ID_4275296 A-to-I Human chr1 + 15879119 15879111 15879120 CCAGCACACTATGAGGCTGAGGTGGGTAGATCACTTGAGGTCGGTCAGGAGTTCGAGACCAGCCT CCAGCACACTATGAGGCTGAGGTGG_________TTGAGGTCGGTCAGGAGTTCGAGACCAGCCT GGTAGATCAC G SPEN Ensembl:ENSG00000065526 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1211562217 Functional Loss DEL dbSNP153 26..34 33 - - - Human_RBP_ID_10622844 RMVar_hsa_circ_15102,RMVar_hsa_circ_358018,RMVar_hsa_circ_265658,RMVar_hsa_circ_66351,RMVar_hsa_circ_375648,RMVar_hsa_circ_58948,RMVar_hsa_circ_129486 9056 RMVar_ID_9056 Human_SNP_ID_4279033 A-to-I Human chr1 + 15893962 15893962 15893962 TTGTGGCTGAAGCTTAAGAATCACTTGAACCCAGGAAATGGAGGTTGCAATGAGCCAAGATTGCA TTGTGGCTGAAGCTTAAGAATCACTTGAACCCCGGAAATGGAGGTTGCAATGAGCCAAGATTGCA A C SPEN Ensembl:ENSG00000065526 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1401373326 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15102,RMVar_hsa_circ_358018,RMVar_hsa_circ_265658,RMVar_hsa_circ_66351,RMVar_hsa_circ_375648,RMVar_hsa_circ_58948,RMVar_hsa_circ_129486 9057 RMVar_ID_9057 Human_SNP_ID_4284000 A-to-I Human chr1 + 15913479 15913479 15913479 CACCTTGATTGATTGATTGATTGATTGGAGACAGGGTCTCACTCTGTTGCCACCCAGGCTAGAGT CACCTTGATTGATTGATTGATTGATTGGAGACTGGGTCTCACTCTGTTGCCACCCAGGCTAGAGT A T SPEN Ensembl:ENSG00000065526 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs936714116 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15102,RMVar_hsa_circ_265658,RMVar_hsa_circ_58948,RMVar_hsa_circ_127083,RMVar_hsa_circ_12265,RMVar_hsa_circ_299594,RMVar_hsa_circ_344436,RMVar_hsa_circ_74312,RMVar_hsa_circ_271052,RMVar_hsa_circ_129487,RMVar_hsa_circ_129489,RMVar_hsa_circ_129490,RMVar_hsa_circ_129488,RMVar_hsa_circ_304234,RMVar_hsa_circ_59250,RMVar_hsa_circ_279286,RMVar_hsa_circ_129492,RMVar_hsa_circ_129493,RMVar_hsa_circ_129494 9058 RMVar_ID_9058 Human_SNP_ID_4284508 A-to-I Human chr1 + 15915604 15915604 15915604 TCACCCAGCCTGGAGTGCAGTGGCGTGATCACAGTTCACTGCAGCCTCAACTTCCCATTCTCATG TCACCCAGCCTGGAGTGCAGTGGCGTGATCACTGTTCACTGCAGCCTCAACTTCCCATTCTCATG A T SPEN Ensembl:ENSG00000065526 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs948937707 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15102,RMVar_hsa_circ_265658,RMVar_hsa_circ_58948,RMVar_hsa_circ_127083,RMVar_hsa_circ_12265,RMVar_hsa_circ_299594,RMVar_hsa_circ_344436,RMVar_hsa_circ_74312,RMVar_hsa_circ_271052,RMVar_hsa_circ_129487,RMVar_hsa_circ_129489,RMVar_hsa_circ_129490,RMVar_hsa_circ_129488,RMVar_hsa_circ_304234,RMVar_hsa_circ_59250,RMVar_hsa_circ_279286,RMVar_hsa_circ_129492,RMVar_hsa_circ_129493,RMVar_hsa_circ_129494 9059 RMVar_ID_9059 Human_SNP_ID_4284535 A-to-I Human chr1 + 15915692 15915692 15915692 AAATAGCTGAGAATACAGGCGTGCGCCACCATACTTGGCTAATTTTTTGTATTTTTTTTGGTAGA AAATAGCTGAGAATACAGGCGTGCGCCACCATGCTTGGCTAATTTTTTGTATTTTTTTTGGTAGA A G SPEN Ensembl:ENSG00000065526 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1429935018 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15102,RMVar_hsa_circ_265658,RMVar_hsa_circ_58948,RMVar_hsa_circ_127083,RMVar_hsa_circ_12265,RMVar_hsa_circ_299594,RMVar_hsa_circ_344436,RMVar_hsa_circ_74312,RMVar_hsa_circ_271052,RMVar_hsa_circ_129487,RMVar_hsa_circ_129489,RMVar_hsa_circ_129490,RMVar_hsa_circ_129488,RMVar_hsa_circ_304234,RMVar_hsa_circ_59250,RMVar_hsa_circ_279286,RMVar_hsa_circ_129492,RMVar_hsa_circ_129493,RMVar_hsa_circ_129494 9060 RMVar_ID_9060 Human_SNP_ID_4310391 A-to-I Human chr1 - 16014479 16014477 16014480 CCACTGAGTGCTGTGCTTTGTCACTGAAGGTTAGATCTGAACCCAGGGTGTCAACTGCTGCTCTC CCACTGAGTGCTGTGCTTTGTCACTGAAGGT___ATCTGAACCCAGGGTGTCAACTGCTGCTCTC TCTA T HSPB7 Ensembl:ENSG00000173641 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1378271704 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_129503,RMVar_hsa_circ_119836 9061 RMVar_ID_9061 Human_SNP_ID_4310393 A-to-I Human chr1 - 16014479 16014479 16014479 CCACTGAGTGCTGTGCTTTGTCACTGAAGGTTAGATCTGAACCCAGGGTGTCAACTGCTGCTCTC CCACTGAGTGCTGTGCTTTGTCACTGAAGGTTTGATCTGAACCCAGGGTGTCAACTGCTGCTCTC T A HSPB7 Ensembl:ENSG00000173641 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1291501442 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_129503,RMVar_hsa_circ_119836 9062 RMVar_ID_9062 Human_SNP_ID_4328807 A-to-I Human chr1 - 16070587 16070587 16070587 GGCTCTCACTATGTTGCCCAGGCTTATCTCGAACTCCTGGCCTCAAGCCACCCTCCCACCTCGGC GGCTCTCACTATGTTGCCCAGGCTTATCTCGAGCTCCTGGCCTCAAGCCACCCTCCCACCTCGGC T C FAM131C Ensembl:ENSG00000185519 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1421527817 Functional Loss SNV dbSNP153 33..33 33 - - - 9063 RMVar_ID_9063 Human_SNP_ID_4370945 A-to-I Human chr1 - 16224418 16224418 16224418 TGACTGCAGCCTCTACCTCCCAGGTTCAAATTATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGA TGACTGCAGCCTCTACCTCCCAGGTTCAAATTGTTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGA T C ANO7L1 Ensembl:ENSG00000237276 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1394641381 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17340394 9064 RMVar_ID_9064 Human_SNP_ID_4372053 A-to-I Human chr1 - 16229035 16229035 16229035 GCACTCCAGCCTGGGCAACAGAGTGAGACTCTATCTCAAAAACAAAACAAAACAAACAACAAAAA GCACTCCAGCCTGGGCAACAGAGTGAGACTCTGTCTCAAAAACAAAACAAAACAAACAACAAAAA T C AL109627.1 Ensembl:ENSG00000288398 lincRNA exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1312434675 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26370868 9065 RMVar_ID_9065 Human_SNP_ID_4372066 A-to-I Human chr1 - 16229073 16229073 16229073 AGGAGGCGGAGGTTGCAGTGAGCCAAGATTACACTACTGCACTCCAGCCTGGGCAACAGAGTGAG AGGAGGCGGAGGTTGCAGTGAGCCAAGATTACGCTACTGCACTCCAGCCTGGGCAACAGAGTGAG T C AL109627.1 Ensembl:ENSG00000288398 lincRNA exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1472525774 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24601696 9066 RMVar_ID_9066 Human_SNP_ID_4372086 A-to-I Human chr1 - 16229111 16229111 16229111 CTACTCAGGAGGCTGAGGCACGAGAATCGCTTAAACCCAGGAGGCGGAGGTTGCAGTGAGCCAAG CTACTCAGGAGGCTGAGGCACGAGAATCGCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCCAAG T C AL109627.1 Ensembl:ENSG00000288398 lincRNA exon GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1282078644 Functional Loss SNV dbSNP153 33..33 33 - - - 9067 RMVar_ID_9067 Human_SNP_ID_4372172 A-to-I Human chr1 - 16229493 16229491 16229493 CTTGCTGATGCCCTTCTTATTTTTTTAGAGACAGGGTCTTGCTCTGTCGCCCAGGCTGGAGTGCA CTTGCTGATGCCCTTCTTATTTTTTTAGAGAC__GGTCTTGCTCTGTCGCCCAGGCTGGAGTGCA CCT C AL109627.1 Ensembl:ENSG00000288398 lincRNA exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1229278059 Functional Loss DEL dbSNP153 33..34 33 - - - 9068 RMVar_ID_9068 Human_SNP_ID_4372574 A-to-I Human chr1 - 16231085 16231085 16231085 CCTCAAATAATCCGCTCGCCACAGCCTCCGAAAATGCTGGGATTACAGGCACGAGCCACTGCGCC CCTCAAATAATCCGCTCGCCACAGCCTCCGAACATGCTGGGATTACAGGCACGAGCCACTGCGCC T G AL109627.1 Ensembl:ENSG00000288398 lincRNA exon GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs944121769 Functional Loss SNV dbSNP153 33..33 33 - - - 9069 RMVar_ID_9069 Human_SNP_ID_4372618 A-to-I Human chr1 - 16231249 16231249 16231249 TCAGCTCACTGCAACCTACACCTCCTGGGTTCAAGCGATTCTCCTGCCACAGCCTCCCAAGTAGC TCAGCTCACTGCAACCTACACCTCCTGGGTTCGAGCGATTCTCCTGCCACAGCCTCCCAAGTAGC T C AL109627.1 Ensembl:ENSG00000288398 lincRNA exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1271687587 Functional Loss SNV dbSNP153 33..33 33 - - - 9070 RMVar_ID_9070 Human_SNP_ID_4383994 A-to-I Human chr1 - 16277568 16277568 16277568 GGTGCATACCACCACGCCCGGCTAGTTTTTGTATTTTTAGTAGAGATAGGGTTTCACCGTGTTGG GGTGCATACCACCACGCCCGGCTAGTTTTTGTGTTTTTAGTAGAGATAGGGTTTCACCGTGTTGG T C FBXO42 Ensembl:ENSG00000037637 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1189806820 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54825,RMVar_hsa_circ_337018,RMVar_hsa_circ_129532 9071 RMVar_ID_9071 Human_SNP_ID_4386199 A-to-I Human chr1 - 16285891 16285891 16285891 TGCACTGCAGTCTGGGTGACGAAGCAAGTCCTATCTCAAAAAGAACAACAAAAACAAAAAAGAGA TGCACTGCAGTCTGGGTGACGAAGCAAGTCCTGTCTCAAAAAGAACAACAAAAACAAAAAAGAGA T C FBXO42 Ensembl:ENSG00000037637 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1396821416 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54825,RMVar_hsa_circ_337018,RMVar_hsa_circ_129532 9072 RMVar_ID_9072 Human_SNP_ID_4387917 A-to-I Human chr1 - 16293258 16293258 16293258 AAATTAGCTGGGCATGGTGATGGGTACCTGTAATCCCACCTACTTGGGAGGCTGAGGCAGGAGAA AAATTAGCTGGGCATGGTGATGGGTACCTGTAGTCCCACCTACTTGGGAGGCTGAGGCAGGAGAA T C FBXO42 Ensembl:ENSG00000037637 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893934833 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54825,RMVar_hsa_circ_337018,RMVar_hsa_circ_129532 9073 RMVar_ID_9073 Human_SNP_ID_4391371 A-to-I Human chr1 - 16307385 16307385 16307385 GTGATCCTCCCTCCTCTGCCTCCCAAGTAGCTAGGACTACAAGTGCAGACCACCATGCCTGGCTA GTGATCCTCCCTCCTCTGCCTCCCAAGTAGCTGGGACTACAAGTGCAGACCACCATGCCTGGCTA T C FBXO42 Ensembl:ENSG00000037637 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1345810080 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_129536,RMVar_hsa_circ_284212,RMVar_hsa_circ_129535,RMVar_hsa_circ_129538,RMVar_hsa_circ_284569 9074 RMVar_ID_9074 Human_SNP_ID_4391560 A-to-I Human chr1 - 16308247 16308247 16308247 GCTGGACACAGTGGCTCACGCCTGTAATTCCAACACTTTGAGAGGCTGAGATGGGAGGAACACTT GCTGGACACAGTGGCTCACGCCTGTAATTCCAGCACTTTGAGAGGCTGAGATGGGAGGAACACTT T C FBXO42 Ensembl:ENSG00000037637 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs764775550 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_129536,RMVar_hsa_circ_284212,RMVar_hsa_circ_129535,RMVar_hsa_circ_129538,RMVar_hsa_circ_284569 9075 RMVar_ID_9075 Human_SNP_ID_4391561 A-to-I Human chr1 - 16308254 16308254 16308254 AGTAAAGGCTGGACACAGTGGCTCACGCCTGTAATTCCAACACTTTGAGAGGCTGAGATGGGAGG AGTAAAGGCTGGACACAGTGGCTCACGCCTGTGATTCCAACACTTTGAGAGGCTGAGATGGGAGG T C FBXO42 Ensembl:ENSG00000037637 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1322590569 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_129536,RMVar_hsa_circ_284212,RMVar_hsa_circ_129535,RMVar_hsa_circ_129538,RMVar_hsa_circ_284569 9076 RMVar_ID_9076 Human_SNP_ID_4391588 A-to-I Human chr1 - 16308368 16308368 16308368 AGCGATCCTCCTGCCTTGCTTCTCATGTAGCTAGGACCACAGGCATACACCACTGAGCCTGGCAA AGCGATCCTCCTGCCTTGCTTCTCATGTAGCTGGGACCACAGGCATACACCACTGAGCCTGGCAA T C FBXO42 Ensembl:ENSG00000037637 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11806312 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_129536,RMVar_hsa_circ_284212,RMVar_hsa_circ_129535,RMVar_hsa_circ_129538,RMVar_hsa_circ_284569 9077 RMVar_ID_9077 Human_SNP_ID_4391899 A-to-I Human chr1 - 16309205 16309205 16309205 AAATTAGCTGGGTATGGTGGCGCGTGCCTGTAATCCCAGCTACTTGGAAGTCTGAGGCAGGAGAA AAATTAGCTGGGTATGGTGGCGCGTGCCTGTAGTCCCAGCTACTTGGAAGTCTGAGGCAGGAGAA T C FBXO42 Ensembl:ENSG00000037637 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs927275848 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_129536,RMVar_hsa_circ_284212,RMVar_hsa_circ_129535,RMVar_hsa_circ_129538,RMVar_hsa_circ_284569 9078 RMVar_ID_9078 Human_SNP_ID_4392232 A-to-I Human chr1 - 16310474 16310474 16310474 CACGCTGGAGTCTAGTGGCGTGATCAGGGCTCACTGCAGACTCAACCTCCCAGGCTCAAGCAATC CACGCTGGAGTCTAGTGGCGTGATCAGGGCTCCCTGCAGACTCAACCTCCCAGGCTCAAGCAATC T G FBXO42 Ensembl:ENSG00000037637 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs937628815 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_741362,Human_RBP_ID_19216980 RMVar_hsa_circ_129536,RMVar_hsa_circ_284212,RMVar_hsa_circ_129535,RMVar_hsa_circ_129538,RMVar_hsa_circ_284569 9079 RMVar_ID_9079 Human_SNP_ID_4392965 A-to-I Human chr1 - 16312959 16312959 16312959 GAAACCTCATCTCTACTAAAAATACAAAAATTAGTGAGGCATGGTGGTGGGTGCCTGTAGTCCTA GAAACCTCATCTCTACTAAAAATACAAAAATTCGTGAGGCATGGTGGTGGGTGCCTGTAGTCCTA T G FBXO42 Ensembl:ENSG00000037637 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1173028662 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_129536,RMVar_hsa_circ_284212,RMVar_hsa_circ_129535,RMVar_hsa_circ_129538,RMVar_hsa_circ_284569 9080 RMVar_ID_9080 Human_SNP_ID_4393469 A-to-I Human chr1 - 16314797 16314797 16314797 TCACTGCAAGCTCTGCCTCCCGGGGTCATGTTATTCACCTGCCTCAGCCTCCAGAGTAGCTGGGA TCACTGCAAGCTCTGCCTCCCGGGGTCATGTTGTTCACCTGCCTCAGCCTCCAGAGTAGCTGGGA T C FBXO42 Ensembl:ENSG00000037637 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs943263762 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_129536,RMVar_hsa_circ_284212,RMVar_hsa_circ_129535,RMVar_hsa_circ_129538,RMVar_hsa_circ_284569 9081 RMVar_ID_9081 Human_SNP_ID_4393993 A-to-I Human chr1 - 16316501 16316501 16316501 GAACTCCTGACCTAAGGTGATCTGCCGGCCTCAGAATCCCAAAGTGCTGGGACTACAGGTGTGAG GAACTCCTGACCTAAGGTGATCTGCCGGCCTCCGAATCCCAAAGTGCTGGGACTACAGGTGTGAG T G FBXO42 Ensembl:ENSG00000037637 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1014560463 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10635857,Human_RBP_ID_24602410 RMVar_hsa_circ_129536 9082 RMVar_ID_9082 Human_SNP_ID_4396065 A-to-I Human chr1 - 16324785 16324785 16324785 TTGAAACGGAGTCTTGCTGTGTCACCCAGGCTAGAGTGTAGTTGCGCGATCTTGGCTCACTGCAG TTGAAACGGAGTCTTGCTGTGTCACCCAGGCTGGAGTGTAGTTGCGCGATCTTGGCTCACTGCAG T C FBXO42 Ensembl:ENSG00000037637 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1243442241 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_746108 9083 RMVar_ID_9083 Human_SNP_ID_4396290 A-to-I Human chr1 - 16325754 16325754 16325754 GGGCGTGGTGACGCATGCCTATAATCCCAGCTACTCTGGAGGCTGAGGTAGGAGAATCGCTCGAG GGGCGTGGTGACGCATGCCTATAATCCCAGCTGCTCTGGAGGCTGAGGTAGGAGAATCGCTCGAG T C FBXO42 Ensembl:ENSG00000037637 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444237650 Functional Loss SNV dbSNP153 33..33 33 - - - 9084 RMVar_ID_9084 Human_SNP_ID_4398006 A-to-I Human chr1 - 16332010 16332010 16332010 AGTTTTGCTCTTGTTGCCCAGACTGGAGTGCAATGGCACGATCTCGGCTCAACACAACCTTCACC AGTTTTGCTCTTGTTGCCCAGACTGGAGTGCAGTGGCACGATCTCGGCTCAACACAACCTTCACC T C FBXO42 Ensembl:ENSG00000037637 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1354976228 Functional Loss SNV dbSNP153 33..33 33 - - - 9085 RMVar_ID_9085 Human_SNP_ID_4399010 A-to-I Human chr1 - 16335615 16335615 16335615 GTGATCCACCCGCCTCGGCCTCCCAAAGTGGTAGGATTACAGGTATGAGCCACTGTGCCTGGCCC GTGATCCACCCGCCTCGGCCTCCCAAAGTGGTTGGATTACAGGTATGAGCCACTGTGCCTGGCCC T A FBXO42 Ensembl:ENSG00000037637 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1370847934 Functional Loss SNV dbSNP153 33..33 33 - - - 9086 RMVar_ID_9086 Human_SNP_ID_4399177 A-to-I Human chr1 - 16336180 16336180 16336180 TAATCCCAACACTTCGGGAGGCTGAGGTAGGCAGGTCACCTGAGGTCAGGAGTTCAAGATCAGCC TAATCCCAACACTTCGGGAGGCTGAGGTAGGCGGGTCACCTGAGGTCAGGAGTTCAAGATCAGCC T C FBXO42 Ensembl:ENSG00000037637 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1019126692 Functional Loss SNV dbSNP153 33..33 33 - - - 9087 RMVar_ID_9087 Human_SNP_ID_4399198 A-to-I Human chr1 - 16336238 16336238 16336238 AGAGTGAGGAGAGGCACACAAAAAGTAAGATTAGGCCAGACGCGGTGGCTCATGCCTGTAATCCC AGAGTGAGGAGAGGCACACAAAAAGTAAGATTTGGCCAGACGCGGTGGCTCATGCCTGTAATCCC T A FBXO42 Ensembl:ENSG00000037637 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs934509444 Functional Loss SNV dbSNP153 33..33 33 - - - 9088 RMVar_ID_9088 Human_SNP_ID_4399247 A-to-I Human chr1 - 16336434 16336434 16336434 GAGCTGCTTTAACCCAGGAGGTGGAGGTTGCAATGAGCCAAGATCACGCCACTGCTCCCCAGCCT GAGCTGCTTTAACCCAGGAGGTGGAGGTTGCAGTGAGCCAAGATCACGCCACTGCTCCCCAGCCT T C FBXO42 Ensembl:ENSG00000037637 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs768349560 Functional Loss SNV dbSNP153 33..33 33 - - - 9089 RMVar_ID_9089 Human_SNP_ID_4399442 A-to-I Human chr1 - 16337322 16337322 16337322 CTGTTGATTCCATTTTCTCATCTAGTGTTGATACCAGCTACATTTTAATGGTTACTGAAGACCTT CTGTTGATTCCATTTTCTCATCTAGTGTTGATGCCAGCTACATTTTAATGGTTACTGAAGACCTT T C FBXO42 Ensembl:ENSG00000037637 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs553550244 Functional Loss SNV dbSNP153 33..33 33 - - - 9090 RMVar_ID_9090 Human_SNP_ID_4400402 A-to-I Human chr1 - 16340421 16340421 16340421 AGCTACTCGGGAGGCTGAGGCAGGAGAATTGCATGAACCTGGGAGAGGCGGAGGCTGCAGTGAGC AGCTACTCGGGAGGCTGAGGCAGGAGAATTGCGTGAACCTGGGAGAGGCGGAGGCTGCAGTGAGC T C FBXO42 Ensembl:ENSG00000037637 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1337182102 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17556986 9091 RMVar_ID_9091 Human_SNP_ID_4407294 A-to-I Human chr1 + 16364326 16364326 16364326 CACCACGCCTGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGTCGGGCTGG CACCACGCCTGGCTAATTTTTGTATTTTTAGTGGAGACGGGGTTTCACCATGTTGGTCGGGCTGG A G SZRD1 Ensembl:ENSG00000055070 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1039666441 Functional Loss SNV dbSNP153 33..33 33 - - - 9092 RMVar_ID_9092 Human_SNP_ID_4409239 A-to-I Human chr1 + 16371308 16371308 16371308 AATTTCTGTCTCAGGCAATCTCCACCCGCCTCAGCCTCCCAAGGTGCTGGGATTACAGGCATGAG AATTTCTGTCTCAGGCAATCTCCACCCGCCTCGGCCTCCCAAGGTGCTGGGATTACAGGCATGAG A G SZRD1 Ensembl:ENSG00000055070 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1224668194 Functional Loss SNV dbSNP153 33..33 33 - - - 9093 RMVar_ID_9093 Human_SNP_ID_4409943 A-to-I Human chr1 + 16373743 16373743 16373743 CTTCAGCCTCAACCTCCCGAGTAGCTGGGACTACAGGCATGCGCCACCACACCTGACTATTTTTG CTTCAGCCTCAACCTCCCGAGTAGCTGGGACTGCAGGCATGCGCCACCACACCTGACTATTTTTG A G SZRD1 Ensembl:ENSG00000055070 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1023860354 Functional Loss SNV dbSNP153 33..33 33 - - - 9094 RMVar_ID_9094 Human_SNP_ID_4410365 A-to-I Human chr1 + 16375364 16375364 16375364 TTGAGAAGGAGTTTCTCTCTGTCACCCAGGCTAGAGTGCAGTGGCGCAATTTCTGCTCACTGAAC TTGAGAAGGAGTTTCTCTCTGTCACCCAGGCTGGAGTGCAGTGGCGCAATTTCTGCTCACTGAAC A G SZRD1 Ensembl:ENSG00000055070 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs544611704 Functional Loss SNV dbSNP153 33..33 33 - - - 9095 RMVar_ID_9095 Human_SNP_ID_4410407 A-to-I Human chr1 + 16375581 16375581 16375581 GCAGTCTGCCCACATCGGCCTCCCAAAGTGTTAGGATTACAGGCGTGAGCCACCGCGCCCGGTCC GCAGTCTGCCCACATCGGCCTCCCAAAGTGTTCGGATTACAGGCGTGAGCCACCGCGCCCGGTCC A C SZRD1 Ensembl:ENSG00000055070 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006652828 Functional Loss SNV dbSNP153 33..33 33 - - - 9096 RMVar_ID_9096 Human_SNP_ID_4410898 A-to-I Human chr1 + 16377464 16377464 16377464 AAAATGAGCGGGACGTGGTCGTGTGCACCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGGGA AAAATGAGCGGGACGTGGTCGTGTGCACCTGTGATCCCAGCTACTCAGGAGGCTGAGGCAGGGGA A G SZRD1 Ensembl:ENSG00000055070 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs527819923 Functional Loss SNV dbSNP153 33..33 33 - - - 9097 RMVar_ID_9097 Human_SNP_ID_4411373 A-to-I Human chr1 + 16379299 16379299 16379299 CTGCCACCACGCCCGGCTAATTTTTTGTTTTTAGTAGAGACGGGGTTTTACCATGTTAGCCAGAA CTGCCACCACGCCCGGCTAATTTTTTGTTTTTGGTAGAGACGGGGTTTTACCATGTTAGCCAGAA A G SZRD1 Ensembl:ENSG00000055070 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1041002941 Functional Loss SNV dbSNP153 33..33 33 - - - 9098 RMVar_ID_9098 Human_SNP_ID_4411375 A-to-I Human chr1 + 16379302 16379302 16379302 CCACCACGCCCGGCTAATTTTTTGTTTTTAGTAGAGACGGGGTTTTACCATGTTAGCCAGAATGG CCACCACGCCCGGCTAATTTTTTGTTTTTAGTGGAGACGGGGTTTTACCATGTTAGCCAGAATGG A G SZRD1 Ensembl:ENSG00000055070 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs901794296 Functional Loss SNV dbSNP153 33..33 33 - - - 9099 RMVar_ID_9099 Human_SNP_ID_4411902 A-to-I Human chr1 + 16381131 16381131 16381131 AAAAAACTAGCCAGGTGTGGTGGCACATGCCTATAATCCCAGCTGCTCAGGAGGCCGAGGCCGAA AAAAAACTAGCCAGGTGTGGTGGCACATGCCTGTAATCCCAGCTGCTCAGGAGGCCGAGGCCGAA A G SZRD1 Ensembl:ENSG00000055070 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1269579007 Functional Loss SNV dbSNP153 33..33 33 - - - 9100 RMVar_ID_9100 Human_SNP_ID_4411920 A-to-I Human chr1 + 16381169 16381169 16381169 CCAGCTGCTCAGGAGGCCGAGGCCGAAGGATCACTTGAGTCCAGGAGTGTGAGGCTGCAGTGAGC CCAGCTGCTCAGGAGGCCGAGGCCGAAGGATCGCTTGAGTCCAGGAGTGTGAGGCTGCAGTGAGC A G SZRD1 Ensembl:ENSG00000055070 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1045462390 Functional Loss SNV dbSNP153 33..33 33 - - - 9101 RMVar_ID_9101 Human_SNP_ID_4411923 A-to-I Human chr1 + 16381179 16381179 16381179 AGGAGGCCGAGGCCGAAGGATCACTTGAGTCCAGGAGTGTGAGGCTGCAGTGAGCTGTGATTGTA AGGAGGCCGAGGCCGAAGGATCACTTGAGTCCGGGAGTGTGAGGCTGCAGTGAGCTGTGATTGTA A G SZRD1 Ensembl:ENSG00000055070 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs936013693 Functional Loss SNV dbSNP153 33..33 33 - - - 9102 RMVar_ID_9102 Human_SNP_ID_4412434 A-to-I Human chr1 + 16382919 16382919 16382919 ACGGAGTCTCACTCTCTCCCCCCTGCTAGAGTACAATGGTGCAATCTCAGCTTACTGCAACCTCC ACGGAGTCTCACTCTCTCCCCCCTGCTAGAGTGCAATGGTGCAATCTCAGCTTACTGCAACCTCC A G SZRD1 Ensembl:ENSG00000055070 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1303218534 Functional Loss SNV dbSNP153 33..33 33 - - - 9103 RMVar_ID_9103 Human_SNP_ID_4412809 A-to-I Human chr1 + 16384356 16384356 16384356 AGCCCACAGTTCAAGAGCAGCCTGGAGAACATAGCAAGACCCCGTCTCCACCAAAAAAAAAAAAA AGCCCACAGTTCAAGAGCAGCCTGGAGAACATGGCAAGACCCCGTCTCCACCAAAAAAAAAAAAA A G SZRD1 Ensembl:ENSG00000055070 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1269399736 Functional Loss SNV dbSNP153 33..33 33 - - - 9104 RMVar_ID_9104 Human_SNP_ID_4423727 A-to-I Human chr1 - 16425175 16425155 16425176 GGGCATGGTGGCTCACGCCTGTTAATCCCAGCACTTCTGGAGGCCGAAGGAGGCAGATCACCTGA GGGCATGGTGGCTCACGCCTGTTAATCCCAG_____________________GCAGATCACCTGA CCTCCTTCGGCCTCCAGAAGTG C SPATA21 Ensembl:ENSG00000187144 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1434294554 Functional Loss DEL dbSNP153 32..52 33 - - - Human_Splice_Rec_22260,Human_Splice_Rec_22266 9105 RMVar_ID_9105 Human_SNP_ID_4429130 A-to-I Human chr1 + 16446402 16446402 16446402 CAGCCTGGGCAACATATCAAGACCCTATCTCTAACAAAAATTGAGTGGGCATGGTGGCATGTGCC CAGCCTGGGCAACATATCAAGACCCTATCTCTTACAAAAATTGAGTGGGCATGGTGGCATGTGCC A T NECAP2 Ensembl:ENSG00000157191 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1016795388 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557632 RMVar_hsa_circ_22607,RMVar_hsa_circ_351991,RMVar_hsa_circ_89132,RMVar_hsa_circ_129542,RMVar_hsa_circ_129543 9106 RMVar_ID_9106 Human_SNP_ID_4429144 A-to-I Human chr1 + 16446444 16446444 16446444 GAGTGGGCATGGTGGCATGTGCCTGTATTCCCAGCTACGTGAGAGGCTGAAGCGGGAAGATTACT GAGTGGGCATGGTGGCATGTGCCTGTATTCCCGGCTACGTGAGAGGCTGAAGCGGGAAGATTACT A G NECAP2 Ensembl:ENSG00000157191 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1230885302 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17556542 RMVar_hsa_circ_22607,RMVar_hsa_circ_351991,RMVar_hsa_circ_89132,RMVar_hsa_circ_129542,RMVar_hsa_circ_129543 9107 RMVar_ID_9107 Human_SNP_ID_4433041 A-to-I Human chr1 + 16460865 16460865 16460865 ACCTCAAGTTATCTGCCCGCCTTGGCCTCCCAAAGTGCTGGGATTATAGGCGTGAGCCACGGCAC ACCTCAAGTTATCTGCCCGCCTTGGCCTCCCAGAGTGCTGGGATTATAGGCGTGAGCCACGGCAC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1021410961 Functional Loss SNV dbSNP153 33..33 33 - - - 9108 RMVar_ID_9108 Human_SNP_ID_4434583 A-to-I Human chr1 - 16466294 16466294 16466294 TCAAGCGATTCTCCTGCCTCAGCCTCTCTAGTAGCTAGGACTACAGGCGTGTGCCACCACACCCG TCAAGCGATTCTCCTGCCTCAGCCTCTCTAGTGGCTAGGACTACAGGCGTGTGCCACCACACCCG T C lnc-SPATA21-4,lnc-SPATA21-4:2 RNACentral:URS0000D5B66F,RNACentral:URS0000D59833 lincRNA,lincRNA intron,intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1416252492 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24603662 9109 RMVar_ID_9109 Human_SNP_ID_4434806 A-to-I Human chr1 - 16467158 16467158 16467158 CAGTTCACCTCCTGAGTTCAAGCGCTCCTCCTACCTCAGCCTTTCAAAGAGCTGGAACTACAGGC CAGTTCACCTCCTGAGTTCAAGCGCTCCTCCTTCCTCAGCCTTTCAAAGAGCTGGAACTACAGGC T A lnc-SPATA21-4,lnc-SPATA21-4:2 RNACentral:URS0000D5B66F,RNACentral:URS0000D59833 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs888088999 Functional Loss SNV dbSNP153 33..33 33 - - - 9110 RMVar_ID_9110 Human_SNP_ID_4434807 A-to-I Human chr1 - 16467158 16467158 16467158 CAGTTCACCTCCTGAGTTCAAGCGCTCCTCCTACCTCAGCCTTTCAAAGAGCTGGAACTACAGGC CAGTTCACCTCCTGAGTTCAAGCGCTCCTCCTCCCTCAGCCTTTCAAAGAGCTGGAACTACAGGC T G lnc-SPATA21-4,lnc-SPATA21-4:2 RNACentral:URS0000D5B66F,RNACentral:URS0000D59833 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs888088999 Functional Loss SNV dbSNP153 33..33 33 - - - 9111 RMVar_ID_9111 Human_SNP_ID_4435712 A-to-I Human chr1 - 16470888 16470888 16470888 TCGATCTCCTGACCTCATGATCCACCCACTTCAGCTTCCCAAAGTGCTGGGATTACAGGTGTGAG TCGATCTCCTGACCTCATGATCCACCCACTTCCGCTTCCCAAAGTGCTGGGATTACAGGTGTGAG T G CROCCP3 Ensembl:ENSG00000080947 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs867176632 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5244982 9112 RMVar_ID_9112 Human_SNP_ID_4435745 A-to-I Human chr1 - 16471000 16471000 16471000 CTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTAGAGGTGCCCACCACCATACCCAGCTAATTTTT CTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTGGAGGTGCCCACCACCATACCCAGCTAATTTTT T C CROCCP3 Ensembl:ENSG00000080947 Pseudogene intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1005373043 Functional Loss SNV dbSNP153 33..33 33 - - - 9113 RMVar_ID_9113 Human_SNP_ID_4436950 A-to-I Human chr1 - 16475468 16475468 16475468 AAAATTAGCTGGGTGTGGTGGCACGCGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGA AAAATTAGCTGGGTGTGGTGGCACGCGCCTGTGGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGA T C CROCCP3 Ensembl:ENSG00000080947 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909437994 Functional Loss SNV dbSNP153 33..33 33 - - - 9114 RMVar_ID_9114 Human_SNP_ID_4443150 A-to-I Human chr1 - 16497904 16497904 16497904 CAACATCTCATCTCTACAACAAGTAAAAAATTAGCCAGGCATGGTGGCATGCACCTGTGGTCCCA CAACATCTCATCTCTACAACAAGTAAAAAATTGGCCAGGCATGGTGGCATGCACCTGTGGTCCCA T C CROCCP3 Ensembl:ENSG00000080947 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1180335995 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1251103 9115 RMVar_ID_9115 Human_SNP_ID_4468476 A-to-I Human chr1 - 16562643 16562643 16562643 TGGTTTTCAAAATTAGAAATGTCCTGTATTCCAATGATCATCCTGTAAACATTTTATCATTTATT TGGTTTTCAAAATTAGAAATGTCCTGTATTCCTATGATCATCCTGTAAACATTTTATCATTTATT T A NBPF1 Ensembl:ENSG00000219481 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs156890 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_99979,Human_RBP_ID_1728735,Human_RBP_ID_26390053 9116 RMVar_ID_9116 Human_SNP_ID_4468477 A-to-I Human chr1 - 16562643 16562643 16562643 TGGTTTTCAAAATTAGAAATGTCCTGTATTCCAATGATCATCCTGTAAACATTTTATCATTTATT TGGTTTTCAAAATTAGAAATGTCCTGTATTCCGATGATCATCCTGTAAACATTTTATCATTTATT T C NBPF1 Ensembl:ENSG00000219481 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs156890 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_99979,Human_RBP_ID_1728735,Human_RBP_ID_26390053 9117 RMVar_ID_9117 Human_SNP_ID_4468548 A-to-I Human chr1 - 16562918 16562918 16562918 GTTTATAGAGGACAGGTCAGCTCTCTGGCTCAATGATCTACATTCTGAAGTTGTCTGAAAATGTC GTTTATAGAGGACAGGTCAGCTCTCTGGCTCAGTGATCTACATTCTGAAGTTGTCTGAAAATGTC T C NBPF1 Ensembl:ENSG00000219481 Protein coding 3'UTR GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1483254657 Functional Loss SNV dbSNP153 33..33 33 - - - 9118 RMVar_ID_9118 Human_SNP_ID_4468590 A-to-I Human chr1 - 16563071 16563070 16563072 ATATCACCACAAATCACACAACAAAAAGGAGAAGAGATATTTTGGGTTCAAAAAAAGTAAAAAGA ATATCACCACAAATCACACAACAAAAAGGAG__GAGATATTTTGGGTTCAAAAAAAGTAAAAAGA CTT C NBPF1 Ensembl:ENSG00000219481 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1295139226 Functional Loss DEL dbSNP153 32..33 33 - - - 9119 RMVar_ID_9119 Human_SNP_ID_4468599 A-to-I Human chr1 - 16563101 16563101 16563101 GACAACTGACCTGTCTCCTTCACATAGTCCATATCACCACAAATCACACAACAAAAAGGAGAAGA GACAACTGACCTGTCTCCTTCACATAGTCCATGTCACCACAAATCACACAACAAAAAGGAGAAGA T C NBPF1 Ensembl:ENSG00000219481 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1187649295 Functional Loss SNV dbSNP153 33..33 33 - - - 9120 RMVar_ID_9120 Human_SNP_ID_4468604 A-to-I Human chr1 - 16563129 16563129 16563129 CAACTGCAGAATGTAGAACACTGAGCAGGACAACTGACCTGTCTCCTTCACATAGTCCATATCAC CAACTGCAGAATGTAGAACACTGAGCAGGACACCTGACCTGTCTCCTTCACATAGTCCATATCAC T G NBPF1 Ensembl:ENSG00000219481 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1176962696 Functional Loss SNV dbSNP153 33..33 33 - - - 9121 RMVar_ID_9121 Human_SNP_ID_4468606 A-to-I Human chr1 - 16563138 16563138 16563138 ATTACCAGACAACTGCAGAATGTAGAACACTGAGCAGGACAACTGACCTGTCTCCTTCACATAGT ATTACCAGACAACTGCAGAATGTAGAACACTGTGCAGGACAACTGACCTGTCTCCTTCACATAGT T A NBPF1 Ensembl:ENSG00000219481 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1440337030 Functional Loss SNV dbSNP153 33..33 33 - - - 9122 RMVar_ID_9122 Human_SNP_ID_4468610 A-to-I Human chr1 - 16563159 16563158 16563159 GCCTGAGTTTCATAGGAGGTAATTACCAGACAACTGCAGAATGTAGAACACTGAGCAGGACAACT GCCTGAGTTTCATAGGAGGTAATTACCAGACA_CTGCAGAATGTAGAACACTGAGCAGGACAACT GT G NBPF1 Ensembl:ENSG00000219481 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1166625193 Functional Loss DEL dbSNP153 33..33 33 - - - 9123 RMVar_ID_9123 Human_SNP_ID_4470184 A-to-I Human chr1 - 16567221 16567221 16567221 ACTCATGCCAGCCCTACAGAAGTGCCTTTTACATATTGGAGCAACAGCGTGTTGGCTGGGCTCTT ACTCATGCCAGCCCTACAGAAGTGCCTTTTACGTATTGGAGCAACAGCGTGTTGGCTGGGCTCTT T C NBPF1 Ensembl:ENSG00000219481 Protein coding CDS GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs752038019 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2103176,Human_RBP_ID_23343530 Human_Splice_Rec_22539,Human_Splice_Rec_22593,Human_Splice_Rec_22629 RMVar_hsa_circ_107471,RMVar_hsa_circ_104548,RMVar_hsa_circ_129548,RMVar_hsa_circ_129549 9124 RMVar_ID_9124 Human_SNP_ID_4490453 A-to-I Human chr1 - 16613477 16613469 16613478 GGAGGCGTAGGTGAGGGTCGCGAGGCTGCCCGAGCTTCTGAGCGAGCGCGGTGCTTTTGGGAACG GGAGGCGTAGGTGAGGGTCGCGAGGCTGCCC_________AGCGAGCGCGGTGCTTTTGGGAACG TCAGAAGCTC T NBPF1 Ensembl:ENSG00000219481 Protein coding 5'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1300312926 Functional Loss DEL dbSNP153 32..40 33 - - - Human_RBP_ID_4072569,Human_RBP_ID_5413208,Human_RBP_ID_9318629,Human_RBP_ID_17646881,Human_RBP_ID_18414870,Human_RBP_ID_22022870,Human_RBP_ID_26772950,Human_RBP_ID_27835097 9125 RMVar_ID_9125 Human_SNP_ID_4491746 A-to-I Human chr1 - 16618532 16618532 16618532 GCTATTTTACAATGAAAAATAATGCTGCAGAGAGCATTTTTGCACATGTATCGTGGCAGATGTAG GCTATTTTACAATGAAAAATAATGCTGCAGAGGGCATTTTTGCACATGTATCGTGGCAGATGTAG T C CROCCP2 Ensembl:ENSG00000215908 Pseudogene exon GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1050322 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1728831,Human_RBP_ID_3286178,Human_RBP_ID_5890897,Human_RBP_ID_8242513,Human_RBP_ID_10648334,Human_RBP_ID_27581310 9126 RMVar_ID_9126 Human_SNP_ID_4492833 A-to-I Human chr1 - 16622580 16622580 16622580 GCGATTCTCCTGCCTCAGCCTCCCAAGTAGCTAGGACTACATACGTCCGCCACCATGCCCAGCTA GCGATTCTCCTGCCTCAGCCTCCCAAGTAGCTTGGACTACATACGTCCGCCACCATGCCCAGCTA T A CROCCP2 Ensembl:ENSG00000215908 Pseudogene intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1177556377 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56321 9127 RMVar_ID_9127 Human_SNP_ID_4492882 A-to-I Human chr1 - 16622809 16622809 16622809 TTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGTCAAGCTGGTCTCGAACTCTCGACCT TTTTGTATTTTTAGTAGAGACGGGGTTTCACCGTGTTGGTCAAGCTGGTCTCGAACTCTCGACCT T C CROCCP2 Ensembl:ENSG00000215908 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1446440702 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56321 9128 RMVar_ID_9128 Human_SNP_ID_4492897 A-to-I Human chr1 - 16622867 16622867 16622867 CCTGCCTCAGCCTTCCAAGTAGCTGGGATTACAGGCACGCGCCACCATGCCTGGCTAATTTTGTA CCTGCCTCAGCCTTCCAAGTAGCTGGGATTACCGGCACGCGCCACCATGCCTGGCTAATTTTGTA T G CROCCP2 Ensembl:ENSG00000215908 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1216711704 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56321 9129 RMVar_ID_9129 Human_SNP_ID_4493629 A-to-I Human chr1 - 16625461 16625461 16625461 CAAGACCATCCTGGCTAACACGGTGAAACCCTATCTCTACAAAAAATTAGCTGGGTGTGGTGGCA CAAGACCATCCTGGCTAACACGGTGAAACCCTGTCTCTACAAAAAATTAGCTGGGTGTGGTGGCA T C CROCCP2 Ensembl:ENSG00000215908 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1310905749 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9552880,Human_RBP_ID_17339884,Human_RBP_ID_17456870 RMVar_hsa_circ_56321 9130 RMVar_ID_9130 Human_SNP_ID_4495976 A-to-I Human chr1 - 16633348 16633348 16633348 CCATCCCATCCCCATCCTGTGTTCTCTTCCCAAGGGACCCGCTGCAGCTGGGAGGGGAGCTGTCC CCATCCCATCCCCATCCTGTGTTCTCTTCCCAGGGGACCCGCTGCAGCTGGGAGGGGAGCTGTCC T C CROCCP2 Ensembl:ENSG00000215908 Pseudogene intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1170119758 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_853842,Human_RBP_ID_5337040,Human_RBP_ID_5538512,Human_RBP_ID_18967298,Human_RBP_ID_22022873,Human_RBP_ID_22636282,Human_RBP_ID_26313429,Human_RBP_ID_26387503 RMVar_hsa_circ_80199,RMVar_hsa_circ_11074,RMVar_hsa_circ_18591,RMVar_hsa_circ_129558,RMVar_hsa_circ_129559 9131 RMVar_ID_9131 Human_SNP_ID_4497211 A-to-I Human chr1 - 16637515 16637515 16637515 AGTCTTACTCTTGTTGCCCGGGCTGAAGTACAATGACACGATCTCGGCTTACTACAACCTCTGCC AGTCTTACTCTTGTTGCCCGGGCTGAAGTACAGTGACACGATCTCGGCTTACTACAACCTCTGCC T C CROCCP2 Ensembl:ENSG00000215908 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1485911201 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3334073,Human_RBP_ID_10648677,Human_RBP_ID_17341089 RMVar_hsa_circ_80199,RMVar_hsa_circ_11074,RMVar_hsa_circ_18591,RMVar_hsa_circ_129558 9132 RMVar_ID_9132 Human_SNP_ID_4497213 A-to-I Human chr1 - 16637518 16637518 16637518 CAGAGTCTTACTCTTGTTGCCCGGGCTGAAGTACAATGACACGATCTCGGCTTACTACAACCTCT CAGAGTCTTACTCTTGTTGCCCGGGCTGAAGTGCAATGACACGATCTCGGCTTACTACAACCTCT T C CROCCP2 Ensembl:ENSG00000215908 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1227255288 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3334073,Human_RBP_ID_10648677,Human_RBP_ID_17341089 RMVar_hsa_circ_80199,RMVar_hsa_circ_11074,RMVar_hsa_circ_18591,RMVar_hsa_circ_129558 9133 RMVar_ID_9133 Human_SNP_ID_4575189 A-to-I Human chr1 + 16916685 16916685 16916685 GTGCATGCCACCATGCCAGGCCAATTTTTTTTATTTTTTTGGCAGAGATGGAGTCTCACTGTGTT GTGCATGCCACCATGCCAGGCCAATTTTTTTTGTTTTTTTGGCAGAGATGGAGTCTCACTGTGTT A G CROCC Ensembl:ENSG00000058453 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1180520286 Functional Loss SNV dbSNP153 33..33 33 - - - 9134 RMVar_ID_9134 Human_SNP_ID_4575225 A-to-I Human chr1 + 16916787 16916787 16916787 CTCCTACCTTGGCCTCCCAAAGTGTTGGGATCACAGGTGTGAGTCAGTGCACCCGGCTTGCTGTT CTCCTACCTTGGCCTCCCAAAGTGTTGGGATCGCAGGTGTGAGTCAGTGCACCCGGCTTGCTGTT A G CROCC Ensembl:ENSG00000058453 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893017426 Functional Loss SNV dbSNP153 33..33 33 - - - 9135 RMVar_ID_9135 Human_SNP_ID_4584215 A-to-I Human chr1 + 16940820 16940820 16940820 TCCATCACAGCTCACTGTAACCTGGAACTCCCAGACTCAAGCGATCCTCCCACCTCTACCTCCCA TCCATCACAGCTCACTGTAACCTGGAACTCCCCGACTCAAGCGATCCTCCCACCTCTACCTCCCA A C CROCC Ensembl:ENSG00000058453 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1405381580 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_22852 9136 RMVar_ID_9136 Human_SNP_ID_4584683 A-to-I Human chr1 + 16942110 16942109 16942110 TCATTTCACTGCAACCTCCACCTCCTAGGCTTAAGTGATCCTTCCATCTCAGCCTCCTGAGTAGC TCATTTCACTGCAACCTCCACCTCCTAGGCTT_AGTGATCCTTCCATCTCAGCCTCCTGAGTAGC TA T CROCC Ensembl:ENSG00000058453 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1354783849 Functional Loss DEL dbSNP153 33..33 33 - - - 9137 RMVar_ID_9137 Human_SNP_ID_4588610 A-to-I Human chr1 + 16952125 16952125 16952125 TTGGTCAGGGTGTCTCGAACTTTTGACCTCGTAATCTGCCCACCTCGGCCTCCCAAAGTGCTGGG TTGGTCAGGGTGTCTCGAACTTTTGACCTCGTGATCTGCCCACCTCGGCCTCCCAAAGTGCTGGG A G CROCC Ensembl:ENSG00000058453 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1291396490 Functional Loss SNV dbSNP153 33..33 33 - - - 9138 RMVar_ID_9138 Human_SNP_ID_4588654 A-to-I Human chr1 + 16952230 16952227 16952231 CGGTTTGGCCGGTCGTGCTGACTCATGCCTGTAATCCAGCACTTTGGGAGGCCGAGGTGGGCAGA CGGTTTGGCCGGTCGTGCTGACTCATGCCT____TCCAGCACTTTGGGAGGCCGAGGTGGGCAGA TGTAA T CROCC Ensembl:ENSG00000058453 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1473958899 Functional Loss DEL dbSNP153 31..34 33 - - - 9139 RMVar_ID_9139 Human_SNP_ID_4603472 A-to-I Human chr1 - 17000085 17000085 17000085 GCTAGTGCCCGGAGACTGCCTGGTGCTGCCCCAGGAGGGTGGGCTGATGCCCTGTGATGCCGCCC GCTAGTGCCCGGAGACTGCCTGGTGCTGCCCCGGGAGGGTGGGCTGATGCCCTGTGATGCCGCCC T C ATP13A2 Ensembl:ENSG00000159363 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs17855550 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_743622,Human_RBP_ID_853859,Human_RBP_ID_3935254,Human_RBP_ID_4008597,Human_RBP_ID_8738121,Human_RBP_ID_9271000,Human_RBP_ID_9319756,Human_RBP_ID_22428127,Human_RBP_ID_23345349 Human_Splice_Rec_23296,Human_Splice_Rec_23297,Human_Splice_Rec_23348,Human_Splice_Rec_23349,Human_Splice_Rec_23404,Human_Splice_Rec_23405,Human_Splice_Rec_23484,Human_Splice_Rec_23485,Human_Splice_Rec_23494,Human_Splice_Rec_23495,Human_Splice_Rec_23520,Human_Splice_Rec_23521,Human_Splice_Rec_23530,Human_Splice_Rec_23531,Human_Splice_Rec_23556 Human_miRNA_ID_2038259,Human_miRNA_ID_2694849,Human_miRNA_ID_3017239 RMVar_hsa_circ_25781,RMVar_hsa_circ_328524,RMVar_hsa_circ_102872,RMVar_hsa_circ_129577,RMVar_hsa_circ_36658,RMVar_hsa_circ_129578,RMVar_hsa_circ_119555,RMVar_hsa_circ_31922,RMVar_hsa_circ_129579 9140 RMVar_ID_9140 Human_SNP_ID_4613027 A-to-I Human chr1 - 17034581 17034581 17034581 GAGGTCAGGAGTTTGAGACCAGCCTGGCCAACATGGGAAAACCTATCTCTACTAAAAATACAAAA GAGGTCAGGAGTTTGAGACCAGCCTGGCCAACGTGGGAAAACCTATCTCTACTAAAAATACAAAA T C SDHB Ensembl:ENSG00000117118 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1296389528 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112187,RMVar_hsa_circ_129582 9141 RMVar_ID_9141 Human_SNP_ID_4614935 A-to-I Human chr1 - 17042527 17042527 17042527 GCAATCCACCCATTTTAGCTTCCCAAAGTCCTAGGATTACAGGCATGAGCCACAGCACCCAGCCC GCAATCCACCCATTTTAGCTTCCCAAAGTCCTGGGATTACAGGCATGAGCCACAGCACCCAGCCC T C SDHB Ensembl:ENSG00000117118 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs979326123 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112187,RMVar_hsa_circ_129582 9142 RMVar_ID_9142 Human_SNP_ID_4616800 A-to-I Human chr1 - 17049835 17049835 17049835 CAAGACCATCCTGGCTAAAACGGTGAAACCCCATCCCTACTAAAAATACAAAAAAGTTAGCCGGG CAAGACCATCCTGGCTAAAACGGTGAAACCCCTTCCCTACTAAAAATACAAAAAAGTTAGCCGGG T A SDHB Ensembl:ENSG00000117118 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1053666653 Functional Loss SNV dbSNP153 33..33 33 - - - 9143 RMVar_ID_9143 Human_SNP_ID_4616979 A-to-I Human chr1 - 17050564 17050564 17050564 CACCGTACCCTCCGCCTCCCGGATTTCAAGCAATTCTCCTGCCTCGGCCTCCCAAGTAGCTGAGA CACCGTACCCTCCGCCTCCCGGATTTCAAGCAGTTCTCCTGCCTCGGCCTCCCAAGTAGCTGAGA T C SDHB Ensembl:ENSG00000117118 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs957794008 Functional Loss SNV dbSNP153 33..33 33 - - - 9144 RMVar_ID_9144 Human_SNP_ID_4716019 A-to-I Human chr1 - 17414366 17414366 17414366 ACCACTGTGCCCAGCTAATTTTTTTGTATTTTAGTAGAGATGGGTTTCACCATGTTGCCCAGGCT ACCACTGTGCCCAGCTAATTTTTTTGTATTTTTGTAGAGATGGGTTTCACCATGTTGCCCAGGCT T A RCC2 Ensembl:ENSG00000179051 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1156423297 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5718827 RMVar_hsa_circ_64078,RMVar_hsa_circ_113997,RMVar_hsa_circ_129590,RMVar_hsa_circ_129589,RMVar_hsa_circ_39404,RMVar_hsa_circ_373088,RMVar_hsa_circ_61879,RMVar_hsa_circ_371659,RMVar_hsa_circ_129591,RMVar_hsa_circ_83367,RMVar_hsa_circ_16776,RMVar_hsa_circ_129592,RMVar_hsa_circ_129593,RMVar_hsa_circ_125483,RMVar_hsa_circ_129594,RMVar_hsa_circ_68339 9145 RMVar_ID_9145 Human_SNP_ID_4716163 A-to-I Human chr1 - 17414724 17414724 17414724 GGGAGGCTGAGGTAGGAGAATCGCTTGAGCCCAGGAGGTGGAGGTTGTGGTGAGCCGTGATCGTG GGGAGGCTGAGGTAGGAGAATCGCTTGAGCCCGGGAGGTGGAGGTTGTGGTGAGCCGTGATCGTG T C RCC2 Ensembl:ENSG00000179051 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs889418612 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24754715 RMVar_hsa_circ_64078,RMVar_hsa_circ_113997,RMVar_hsa_circ_129590,RMVar_hsa_circ_129589,RMVar_hsa_circ_39404,RMVar_hsa_circ_373088,RMVar_hsa_circ_61879,RMVar_hsa_circ_371659,RMVar_hsa_circ_129591,RMVar_hsa_circ_83367,RMVar_hsa_circ_16776,RMVar_hsa_circ_129592,RMVar_hsa_circ_129593,RMVar_hsa_circ_125483,RMVar_hsa_circ_129594,RMVar_hsa_circ_68339 9146 RMVar_ID_9146 Human_SNP_ID_4716164 A-to-I Human chr1 - 17414724 17414724 17414724 GGGAGGCTGAGGTAGGAGAATCGCTTGAGCCCAGGAGGTGGAGGTTGTGGTGAGCCGTGATCGTG GGGAGGCTGAGGTAGGAGAATCGCTTGAGCCCCGGAGGTGGAGGTTGTGGTGAGCCGTGATCGTG T G RCC2 Ensembl:ENSG00000179051 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs889418612 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24754715 RMVar_hsa_circ_64078,RMVar_hsa_circ_113997,RMVar_hsa_circ_129590,RMVar_hsa_circ_129589,RMVar_hsa_circ_39404,RMVar_hsa_circ_373088,RMVar_hsa_circ_61879,RMVar_hsa_circ_371659,RMVar_hsa_circ_129591,RMVar_hsa_circ_83367,RMVar_hsa_circ_16776,RMVar_hsa_circ_129592,RMVar_hsa_circ_129593,RMVar_hsa_circ_125483,RMVar_hsa_circ_129594,RMVar_hsa_circ_68339 9147 RMVar_ID_9147 Human_SNP_ID_4716175 A-to-I Human chr1 - 17414747 17414747 17414747 GCACACCCAAGTCCTAGCGACTTGGGAGGCTGAGGTAGGAGAATCGCTTGAGCCCAGGAGGTGGA GCACACCCAAGTCCTAGCGACTTGGGAGGCTGCGGTAGGAGAATCGCTTGAGCCCAGGAGGTGGA T G RCC2 Ensembl:ENSG00000179051 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031240329 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10668055 RMVar_hsa_circ_64078,RMVar_hsa_circ_113997,RMVar_hsa_circ_129590,RMVar_hsa_circ_129589,RMVar_hsa_circ_39404,RMVar_hsa_circ_373088,RMVar_hsa_circ_61879,RMVar_hsa_circ_371659,RMVar_hsa_circ_129591,RMVar_hsa_circ_83367,RMVar_hsa_circ_16776,RMVar_hsa_circ_129592,RMVar_hsa_circ_129593,RMVar_hsa_circ_125483,RMVar_hsa_circ_129594,RMVar_hsa_circ_68339 9148 RMVar_ID_9148 Human_SNP_ID_4716213 A-to-I Human chr1 - 17414893 17414893 17414893 AATCCAGGCCGGGCGCAGTGGTTCATGTTTGTAATCAGAGGACTTTGGGAGGCCAAGGTGGGCAG AATCCAGGCCGGGCGCAGTGGTTCATGTTTGTCATCAGAGGACTTTGGGAGGCCAAGGTGGGCAG T G RCC2 Ensembl:ENSG00000179051 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1438041337 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10668059 RMVar_hsa_circ_64078,RMVar_hsa_circ_113997,RMVar_hsa_circ_129590,RMVar_hsa_circ_129589,RMVar_hsa_circ_39404,RMVar_hsa_circ_373088,RMVar_hsa_circ_61879,RMVar_hsa_circ_371659,RMVar_hsa_circ_129591,RMVar_hsa_circ_83367,RMVar_hsa_circ_16776,RMVar_hsa_circ_129592,RMVar_hsa_circ_129593,RMVar_hsa_circ_125483,RMVar_hsa_circ_129594,RMVar_hsa_circ_68339 9149 RMVar_ID_9149 Human_SNP_ID_4726768 A-to-I Human chr1 + 17448755 17448755 17448755 GTTGCCCAGGCTGATCTTGAACTCCTGAACTTAAGTGATCCTCCCACCTCGGCCTCCCAAAGTAC GTTGCCCAGGCTGATCTTGAACTCCTGAACTTGAGTGATCCTCCCACCTCGGCCTCCCAAAGTAC A G lnc-PADI6-3,lnc-PADI6-3:2,lnc-PADI6-3:3,lnc-ARHGEF10L-1 RNACentral:URS0000D5C1D7,RNACentral:URS0000D5BC11,RNACentral:URS0000D5CADF,RNACentral:URS00008B3D09 lincRNA,lincRNA,lincRNA,lincRNA intron,exon,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1316856780 Functional Loss SNV dbSNP153 33..33 33 - - - 9150 RMVar_ID_9150 Human_SNP_ID_4928785 A-to-I Human chr1 + 18234747 18234747 18234747 AGCATGGGGAAAACCATCTCCATGATCCAATCACCTCCCACCGAGTCCCTTTCACGAACTTGGGA AGCATGGGGAAAACCATCTCCATGATCCAATCTCCTCCCACCGAGTCCCTTTCACGAACTTGGGA A T IGSF21 Ensembl:ENSG00000117154 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs535313402 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_317649,RMVar_hsa_circ_338651 9151 RMVar_ID_9151 Human_SNP_ID_5161813 A-to-I Human chr1 - 19131724 19131724 19131724 GGATTACAGGCATGCGTGACCACGCCCGGCTAATTTTGTATTTTTAGTAGAGATGGGGTTTCTCC GGATTACAGGCATGCGTGACCACGCCCGGCTAGTTTTGTATTTTTAGTAGAGATGGGGTTTCTCC T C UBR4 Ensembl:ENSG00000127481 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1310893840 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_54733,RMVar_hsa_circ_82336,RMVar_hsa_circ_129700,RMVar_hsa_circ_42107,RMVar_hsa_circ_129701,RMVar_hsa_circ_108770,RMVar_hsa_circ_125411,RMVar_hsa_circ_129702 9152 RMVar_ID_9152 Human_SNP_ID_5161814 A-to-I Human chr1 - 19131724 19131724 19131724 GGATTACAGGCATGCGTGACCACGCCCGGCTAATTTTGTATTTTTAGTAGAGATGGGGTTTCTCC GGATTACAGGCATGCGTGACCACGCCCGGCTACTTTTGTATTTTTAGTAGAGATGGGGTTTCTCC T G UBR4 Ensembl:ENSG00000127481 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1310893840 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_54733,RMVar_hsa_circ_82336,RMVar_hsa_circ_129700,RMVar_hsa_circ_42107,RMVar_hsa_circ_129701,RMVar_hsa_circ_108770,RMVar_hsa_circ_125411,RMVar_hsa_circ_129702 9153 RMVar_ID_9153 Human_SNP_ID_5168860 A-to-I Human chr1 - 19158924 19158924 19158924 TTGCCCAGAATGGTCTCGAACAACTGTGCTCAAGTGATTTGTCCACCTCAGCCTCCCAAAGTGCT TTGCCCAGAATGGTCTCGAACAACTGTGCTCAGGTGATTTGTCCACCTCAGCCTCCCAAAGTGCT T C UBR4 Ensembl:ENSG00000127481 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1288392302 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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 9154 RMVar_ID_9154 Human_SNP_ID_5168886 A-to-I Human chr1 - 19159025 19159025 19159025 TCTCATGCCTCACTCAGCCTCCTGAGAAGCTGAGACTGGAGGCATGCACCATCATGCCTGGCTAA TCTCATGCCTCACTCAGCCTCCTGAGAAGCTGGGACTGGAGGCATGCACCATCATGCCTGGCTAA T C UBR4 Ensembl:ENSG00000127481 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1189624259 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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 9155 RMVar_ID_9155 Human_SNP_ID_5168912 A-to-I Human chr1 - 19159108 19159108 19159108 GGAGTCTTGCTCTGTCACCTAGGCTGGAGTGCAGTGGCATGATCTCAGCTTACTGCGACTTCCGC GGAGTCTTGCTCTGTCACCTAGGCTGGAGTGCGGTGGCATGATCTCAGCTTACTGCGACTTCCGC T C UBR4 Ensembl:ENSG00000127481 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1271723608 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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 9156 RMVar_ID_9156 Human_SNP_ID_5171661 A-to-I Human chr1 - 19169472 19169472 19169472 GTCAGTGCAGACTGTGTGTGAGTCCTGGAACAACATCAATACCAATGAATTTCCCAATATTGGAT GTCAGTGCAGACTGTGTGTGAGTCCTGGAACAGCATCAATACCAATGAATTTCCCAATATTGGAT T C UBR4 Ensembl:ENSG00000127481 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1241439642 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_851279,Human_RBP_ID_1417925,Human_RBP_ID_1732321,Human_RBP_ID_5519649,Human_RBP_ID_8740051,Human_RBP_ID_10710992,Human_RBP_ID_18558973,Human_RBP_ID_22851788,Human_RBP_ID_23353380 Human_Splice_Rec_24518,Human_Splice_Rec_24519,Human_Splice_Rec_24896,Human_Splice_Rec_24897 RMVar_hsa_circ_85305,RMVar_hsa_circ_100595,RMVar_hsa_circ_89377,RMVar_hsa_circ_129652,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_103221,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_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_3214,RMVar_hsa_circ_19928,RMVar_hsa_circ_93172,RMVar_hsa_circ_129701,RMVar_hsa_circ_108770,RMVar_hsa_circ_125411,RMVar_hsa_circ_129702,RMVar_hsa_circ_129704,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_129716,RMVar_hsa_circ_129717,RMVar_hsa_circ_129715,RMVar_hsa_circ_92038,RMVar_hsa_circ_129725,RMVar_hsa_circ_90608,RMVar_hsa_circ_129727,RMVar_hsa_circ_377953,RMVar_hsa_circ_110459,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_378523,RMVar_hsa_circ_129736,RMVar_hsa_circ_109927,RMVar_hsa_circ_129740,RMVar_hsa_circ_348402,RMVar_hsa_circ_101270,RMVar_hsa_circ_55599,RMVar_hsa_circ_87922,RMVar_hsa_circ_57917,RMVar_hsa_circ_129742,RMVar_hsa_circ_129743,RMVar_hsa_circ_99860,RMVar_hsa_circ_90321,RMVar_hsa_circ_103879,RMVar_hsa_circ_129746,RMVar_hsa_circ_129747,RMVar_hsa_circ_122928,RMVar_hsa_circ_129749,RMVar_hsa_circ_129751,RMVar_hsa_circ_94494,RMVar_hsa_circ_129750,RMVar_hsa_circ_42469,RMVar_hsa_circ_24623,RMVar_hsa_circ_129755,RMVar_hsa_circ_20138,RMVar_hsa_circ_287420,RMVar_hsa_circ_57692,RMVar_hsa_circ_129753,RMVar_hsa_circ_367244,RMVar_hsa_circ_371081,RMVar_hsa_circ_93158,RMVar_hsa_circ_107229,RMVar_hsa_circ_78531,RMVar_hsa_circ_129757,RMVar_hsa_circ_129758,RMVar_hsa_circ_129759,RMVar_hsa_circ_129756,RMVar_hsa_circ_69721,RMVar_hsa_circ_123901,RMVar_hsa_circ_129754,RMVar_hsa_circ_322224,RMVar_hsa_circ_346308,RMVar_hsa_circ_129760,RMVar_hsa_circ_325044,RMVar_hsa_circ_127615,RMVar_hsa_circ_129761,RMVar_hsa_circ_129762,RMVar_hsa_circ_129763 9157 RMVar_ID_9157 Human_SNP_ID_5180242 A-to-I Human chr1 - 19203316 19203316 19203316 TTGTATTTTTATTAGAGACGGGGTTTCACCATATTGGCCAGGCTGGTCTCGAACTCCTGGCCTCA TTGTATTTTTATTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGGCCTCA T C UBR4 Ensembl:ENSG00000127481 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1017966458 Functional Loss SNV dbSNP153 33..33 33 - - - 9158 RMVar_ID_9158 Human_SNP_ID_5180413 A-to-I Human chr1 - 19204053 19204053 19204053 TGGAGGTTGCAGTGAGCTGAGATAGTGCCACTACATTGTAGCCTGGGCGACAGAGCGAGACTCTG TGGAGGTTGCAGTGAGCTGAGATAGTGCCACTGCATTGTAGCCTGGGCGACAGAGCGAGACTCTG T C UBR4 Ensembl:ENSG00000127481 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1046304386 Functional Loss SNV dbSNP153 33..33 33 - - - 9159 RMVar_ID_9159 Human_SNP_ID_5183268 A-to-I Human chr1 - 19215750 19215750 19215750 CGAACCCAGGAGGCAAAGGCTGCAGTAAGCCGAGATCATGCCTCTGCACTCCAGTCTGGGCAACA CGAACCCAGGAGGCAAAGGCTGCAGTAAGCCGGGATCATGCCTCTGCACTCCAGTCTGGGCAACA T C EMC1 Ensembl:ENSG00000127463 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs532910433 Functional Loss SNV dbSNP153 33..33 33 - - - 9160 RMVar_ID_9160 Human_SNP_ID_5183277 A-to-I Human chr1 - 19215816 19215816 19215816 AATTTAGCCAGGTGTGGTGGTGCATGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAA AATTTAGCCAGGTGTGGTGGTGCATGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAA T C EMC1 Ensembl:ENSG00000127463 Protein coding 3'UTR GSE38233;GSE99789 cultured B-cells;esophageal squamous carcinoma cells,EC109 - 24183664,29796672 RNA-Seq:(High) rs987718450 Functional Loss SNV dbSNP153 33..33 33 - - - 9161 RMVar_ID_9161 Human_SNP_ID_5183290 A-to-I Human chr1 - 19215847 19215846 19215847 TGAAACCCCATCTCTACCAAAAAAATAAAAAAATTTAGCCAGGTGTGGTGGTGCATGCCTGTAAT TGAAACCCCATCTCTACCAAAAAAATAAAAAA_TTTAGCCAGGTGTGGTGGTGCATGCCTGTAAT AT A EMC1 Ensembl:ENSG00000127463 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1558083206 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_24619514 9162 RMVar_ID_9162 Human_SNP_ID_5183291 A-to-I Human chr1 - 19215847 19215847 19215847 TGAAACCCCATCTCTACCAAAAAAATAAAAAAATTTAGCCAGGTGTGGTGGTGCATGCCTGTAAT TGAAACCCCATCTCTACCAAAAAAATAAAAAAGTTTAGCCAGGTGTGGTGGTGCATGCCTGTAAT T C EMC1 Ensembl:ENSG00000127463 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs926070391 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24619514 9163 RMVar_ID_9163 Human_SNP_ID_5183308 A-to-I Human chr1 - 19215921 19215920 19215921 ACTTTGGGAGGCCAAGGCAGGCAGATCATTTGAGGTCAGGAGTTTAAGACCAGCCTGGCCAACAT ACTTTGGGAGGCCAAGGCAGGCAGATCATTTG_GGTCAGGAGTTTAAGACCAGCCTGGCCAACAT CT C EMC1 Ensembl:ENSG00000127463 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1254056765 Functional Loss DEL dbSNP153 33..33 33 - - - 9164 RMVar_ID_9164 Human_SNP_ID_5183315 A-to-I Human chr1 - 19215962 19215962 19215962 CTTTTAGGCGAGGCATGGTGGCTCAAGCCTATAATCCCAGCACTTTGGGAGGCCAAGGCAGGCAG CTTTTAGGCGAGGCATGGTGGCTCAAGCCTATGATCCCAGCACTTTGGGAGGCCAAGGCAGGCAG T C EMC1 Ensembl:ENSG00000127463 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs3208934 Functional Loss SNV dbSNP153 33..33 33 - - - 9165 RMVar_ID_9165 Human_SNP_ID_5183316 A-to-I Human chr1 - 19215964 19215964 19215964 TGCTTTTAGGCGAGGCATGGTGGCTCAAGCCTATAATCCCAGCACTTTGGGAGGCCAAGGCAGGC TGCTTTTAGGCGAGGCATGGTGGCTCAAGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGC T C EMC1 Ensembl:ENSG00000127463 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1929 Functional Loss SNV dbSNP153 33..33 33 - - - 9166 RMVar_ID_9166 Human_SNP_ID_5183318 A-to-I Human chr1 - 19215969 19215969 19215969 AATTTTGCTTTTAGGCGAGGCATGGTGGCTCAAGCCTATAATCCCAGCACTTTGGGAGGCCAAGG AATTTTGCTTTTAGGCGAGGCATGGTGGCTCAGGCCTATAATCCCAGCACTTTGGGAGGCCAAGG T C EMC1 Ensembl:ENSG00000127463 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1056910 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26385400 9167 RMVar_ID_9167 Human_SNP_ID_5183319 A-to-I Human chr1 - 19215970 19215970 19215970 AAATTTTGCTTTTAGGCGAGGCATGGTGGCTCAAGCCTATAATCCCAGCACTTTGGGAGGCCAAG AAATTTTGCTTTTAGGCGAGGCATGGTGGCTCGAGCCTATAATCCCAGCACTTTGGGAGGCCAAG T C EMC1 Ensembl:ENSG00000127463 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1056909 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26385400 9168 RMVar_ID_9168 Human_SNP_ID_5183353 A-to-I Human chr1 - 19216115 19216115 19216115 CTCCCTCCTTAGCCTCCCAAAGTGCCGGGATTACAGGCATGAGCTACTGCACCTGGCCCATAAAT CTCCCTCCTTAGCCTCCCAAAGTGCCGGGATTGCAGGCATGAGCTACTGCACCTGGCCCATAAAT T C EMC1 Ensembl:ENSG00000127463 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1013876010 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26385401 9169 RMVar_ID_9169 Human_SNP_ID_5183357 A-to-I Human chr1 - 19216127 19216126 19216128 GCTGAAGTGATCCTCCCTCCTTAGCCTCCCAAAGTGCCGGGATTACAGGCATGAGCTACTGCACC GCTGAAGTGATCCTCCCTCCTTAGCCTCCCA__GTGCCGGGATTACAGGCATGAGCTACTGCACC CTT C EMC1 Ensembl:ENSG00000127463 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs905230872 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_26373507 9170 RMVar_ID_9170 Human_SNP_ID_5183357 A-to-I Human chr1 - 19216128 19216126 19216128 GGCTGAAGTGATCCTCCCTCCTTAGCCTCCCAAAGTGCCGGGATTACAGGCATGAGCTACTGCAC GGCTGAAGTGATCCTCCCTCCTTAGCCTCCCA__GTGCCGGGATTACAGGCATGAGCTACTGCAC CTT C EMC1 Ensembl:ENSG00000127463 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs905230872 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_26373507 9171 RMVar_ID_9171 Human_SNP_ID_5183358 A-to-I Human chr1 - 19216137 19216137 19216137 GAACACCTGGGCTGAAGTGATCCTCCCTCCTTAGCCTCCCAAAGTGCCGGGATTACAGGCATGAG GAACACCTGGGCTGAAGTGATCCTCCCTCCTTGGCCTCCCAAAGTGCCGGGATTACAGGCATGAG T C EMC1 Ensembl:ENSG00000127463 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs1009004559 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_100985,Human_RBP_ID_5734319,Human_RBP_ID_10711956,Human_RBP_ID_26373507 9172 RMVar_ID_9172 Human_SNP_ID_5183372 A-to-I Human chr1 - 19216191 19216191 19216191 TCTCTGTCACCCAGGCTGGAGAGCAGTGGCACAGTCATAGCTCACTGCAGCCTCGAACACCTGGG TCTCTGTCACCCAGGCTGGAGAGCAGTGGCACCGTCATAGCTCACTGCAGCCTCGAACACCTGGG T G EMC1 Ensembl:ENSG00000127463 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1468468898 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8166798,Human_RBP_ID_23303907,Human_RBP_ID_26373509 9173 RMVar_ID_9173 Human_SNP_ID_5183527 A-to-I Human chr1 - 19216753 19216753 19216753 CTGGGAGGTCGAGGCTGCAGTGAGCCATGAACATGCTACTGCATTCCAGCCTGGGCAACAGAGTG CTGGGAGGTCGAGGCTGCAGTGAGCCATGAACTTGCTACTGCATTCCAGCCTGGGCAACAGAGTG T A EMC1 Ensembl:ENSG00000127463 Protein coding 3'UTR GSE38233;GSE99789;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29796672,32596459,32596459 RNA-Seq:(High) rs1458984448 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4086594,Human_RBP_ID_8166799,Human_RBP_ID_24755675 9174 RMVar_ID_9174 Human_SNP_ID_5183576 A-to-I Human chr1 - 19216962 19216962 19216962 GATTTGGCTGGGCGTGATGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCCATAGTGGAGGAT GATTTGGCTGGGCGTGATGGCTCATGCCTATAGTCCCAGCACTTTGGGAGGCCATAGTGGAGGAT T C EMC1 Ensembl:ENSG00000127463 Protein coding 3'UTR GSE38233;GSE100210;GSE99789;GSE107867;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;ASD brains,cerebellum;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,29796672,30559470,30559470,31158229,31158229 RNA-Seq:(High) rs1277912913 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22369278,Human_RBP_ID_26385406 9175 RMVar_ID_9175 Human_SNP_ID_5183577 A-to-I Human chr1 - 19216963 19216963 19216963 AGATTTGGCTGGGCGTGATGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCCATAGTGGAGGA AGATTTGGCTGGGCGTGATGGCTCATGCCTATTATCCCAGCACTTTGGGAGGCCATAGTGGAGGA T A EMC1 Ensembl:ENSG00000127463 Protein coding 3'UTR GSE38233;GSE100210;GSE99789;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,29796672,30559470,31158229,32596459 RNA-Seq:(High) rs1485170905 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19246790,Human_RBP_ID_22369278,Human_RBP_ID_26385406 9176 RMVar_ID_9176 Human_SNP_ID_5183671 A-to-I Human chr1 - 19217508 19217508 19217508 AAAGCAGGTGCTTTTTTTTTTTTTGAGACAGAATCTCACTCTGTTGCCCAGGCTGGAGTGCAGTG AAAGCAGGTGCTTTTTTTTTTTTTGAGACAGACTCTCACTCTGTTGCCCAGGCTGGAGTGCAGTG T G EMC1 Ensembl:ENSG00000127463 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs1249148103 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26387540 9177 RMVar_ID_9177 Human_SNP_ID_5183672 A-to-I Human chr1 - 19217515 19217509 19217516 TTACCTCAAAGCAGGTGCTTTTTTTTTTTTTGAGACAGAATCTCACTCTGTTGCCCAGGCTGGAG TTACCTCAAAGCAGGTGCTTTTTTTTTTTTT_______AATCTCACTCTGTTGCCCAGGCTGGAG TCTGTCTC T EMC1 Ensembl:ENSG00000127463 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1480065493 Functional Loss DEL dbSNP153 32..38 33 - - - 9178 RMVar_ID_9178 Human_SNP_ID_5192737 A-to-I Human chr1 + 19252790 19252790 19252790 CTCCCACCTCAACCTCCCGAGTAGCTGAGACTACAGGCGCACGCCACCACACCCAGCTAGGTTTT CTCCCACCTCAACCTCCCGAGTAGCTGAGACTGCAGGCGCACGCCACCACACCCAGCTAGGTTTT A G MRTO4 Ensembl:ENSG00000053372 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs950152733 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126069,RMVar_hsa_circ_129813 9179 RMVar_ID_9179 Human_SNP_ID_5193050 A-to-I Human chr1 + 19254111 19254111 19254111 AGAGCAGCAAGGGGCCAGGCATGGTGGCTCACACCTATGATTCCAACACTTTGGGAGACTGAGGT AGAGCAGCAAGGGGCCAGGCATGGTGGCTCACGCCTATGATTCCAACACTTTGGGAGACTGAGGT A G MRTO4 Ensembl:ENSG00000053372 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs757747882 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126069,RMVar_hsa_circ_129813 9180 RMVar_ID_9180 Human_SNP_ID_5194516 A-to-I Human chr1 + 19259059 19259059 19259059 CCGAGGTGGGCAGATCATAAGGTCGGGAGATTAAGACCATCCTGGCTAACACGGTGAAACCCCGT CCGAGGTGGGCAGATCATAAGGTCGGGAGATTGAGACCATCCTGGCTAACACGGTGAAACCCCGT A G MRTO4 Ensembl:ENSG00000053372 Protein coding 3'UTR GSE38233;GSE99789;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;esophageal squamous carcinoma cells,EC109;ASD brains,Fragile X samples from NIH NeuroBioBank;Bronchiolar epithelium,BEP2D cell line - 24183664,29796672,30559470,31158229 RNA-Seq:(High) rs981256879 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_95545,Human_RBP_ID_336738 RMVar_hsa_circ_126069,RMVar_hsa_circ_129813,RMVar_hsa_circ_124214,RMVar_hsa_circ_129814,RMVar_hsa_circ_91823,RMVar_hsa_circ_94120,RMVar_hsa_circ_123635,RMVar_hsa_circ_129816,RMVar_hsa_circ_129818,RMVar_hsa_circ_125107,RMVar_hsa_circ_129819,RMVar_hsa_circ_129820 9181 RMVar_ID_9181 Human_SNP_ID_5194742 A-to-I Human chr1 + 19259964 19259964 19259964 TTTAAAATTTTAAGGAGAGATGGGGTTTCACCATGTTGCCCAGGCTGGTCTCAAACTCCTGAGCT TTTAAAATTTTAAGGAGAGATGGGGTTTCACCCTGTTGCCCAGGCTGGTCTCAAACTCCTGAGCT A C MRTO4 Ensembl:ENSG00000053372 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE99789;GSE107867;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;ASD brains,cerebellum;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line - 23474544,24183664,29129909,29796672,30559470,31158229,31158229,32596459 RNA-Seq:(High) rs982748535 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5734524,Human_RBP_ID_17734642,Human_RBP_ID_22369383,Human_RBP_ID_26373596 RMVar_hsa_circ_126069,RMVar_hsa_circ_129813,RMVar_hsa_circ_124214,RMVar_hsa_circ_129814,RMVar_hsa_circ_91823,RMVar_hsa_circ_94120,RMVar_hsa_circ_123635,RMVar_hsa_circ_129816,RMVar_hsa_circ_129818,RMVar_hsa_circ_125107,RMVar_hsa_circ_129819,RMVar_hsa_circ_129820 9182 RMVar_ID_9182 Human_SNP_ID_5194743 A-to-I Human chr1 + 19259964 19259964 19259964 TTTAAAATTTTAAGGAGAGATGGGGTTTCACCATGTTGCCCAGGCTGGTCTCAAACTCCTGAGCT TTTAAAATTTTAAGGAGAGATGGGGTTTCACCGTGTTGCCCAGGCTGGTCTCAAACTCCTGAGCT A G MRTO4 Ensembl:ENSG00000053372 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE99789;GSE107867;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;ASD brains,cerebellum;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line - 23474544,24183664,29129909,29796672,30559470,31158229,31158229,32596459 RNA-Seq:(High) rs982748535 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5734524,Human_RBP_ID_17734642,Human_RBP_ID_22369383,Human_RBP_ID_26373596 RMVar_hsa_circ_126069,RMVar_hsa_circ_129813,RMVar_hsa_circ_124214,RMVar_hsa_circ_129814,RMVar_hsa_circ_91823,RMVar_hsa_circ_94120,RMVar_hsa_circ_123635,RMVar_hsa_circ_129816,RMVar_hsa_circ_129818,RMVar_hsa_circ_125107,RMVar_hsa_circ_129819,RMVar_hsa_circ_129820 9183 RMVar_ID_9183 Human_SNP_ID_5194756 A-to-I Human chr1 + 19260007 19260007 19260007 GCTGGTCTCAAACTCCTGAGCTCAAGCGATCTACCCACCTTGGCCTCCCAAAGTGCTGGGATTAT GCTGGTCTCAAACTCCTGAGCTCAAGCGATCTGCCCACCTTGGCCTCCCAAAGTGCTGGGATTAT A G MRTO4 Ensembl:ENSG00000053372 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1140996 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22369383 Human_miRNA_ID_1165322,Human_miRNA_ID_2696474 RMVar_hsa_circ_126069,RMVar_hsa_circ_129813,RMVar_hsa_circ_124214,RMVar_hsa_circ_129814,RMVar_hsa_circ_91823,RMVar_hsa_circ_94120,RMVar_hsa_circ_123635,RMVar_hsa_circ_129816,RMVar_hsa_circ_129818,RMVar_hsa_circ_125107,RMVar_hsa_circ_129819,RMVar_hsa_circ_129820 9184 RMVar_ID_9184 Human_SNP_ID_5194760 A-to-I Human chr1 + 19260025 19260025 19260025 AGCTCAAGCGATCTACCCACCTTGGCCTCCCAAAGTGCTGGGATTATAGGTGTGAGCCACCGCAT AGCTCAAGCGATCTACCCACCTTGGCCTCCCAGAGTGCTGGGATTATAGGTGTGAGCCACCGCAT A G MRTO4 Ensembl:ENSG00000053372 Protein coding 3'UTR GSE38233;GSE100210;GSE99789 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 24183664,29129909,29796672 RNA-Seq:(High) rs1248830498 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8167728,Human_RBP_ID_22369384,Human_RBP_ID_26385431 RMVar_hsa_circ_126069,RMVar_hsa_circ_129813,RMVar_hsa_circ_124214,RMVar_hsa_circ_129814,RMVar_hsa_circ_91823,RMVar_hsa_circ_94120,RMVar_hsa_circ_123635,RMVar_hsa_circ_129816,RMVar_hsa_circ_129818,RMVar_hsa_circ_125107,RMVar_hsa_circ_129819,RMVar_hsa_circ_129820 9185 RMVar_ID_9185 Human_SNP_ID_5195465 A-to-I Human chr1 + 19262524 19262524 19262524 GAGGCAGTGGGCGAGAATCCTTGCATTTGGCCAGGCGTGATGGCCACACCTGTAATCCAAGCCCT GAGGCAGTGGGCGAGAATCCTTGCATTTGGCCGGGCGTGATGGCCACACCTGTAATCCAAGCCCT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1289804004 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17734657 9186 RMVar_ID_9186 Human_SNP_ID_5195729 A-to-I Human chr1 + 19263625 19263625 19263625 TCCTCCTATCTTGGCCTCCTAAGGCTGGAACTACAGGCCTATGACACCATGCCTGGCTAGTTTTT TCCTCCTATCTTGGCCTCCTAAGGCTGGAACTGCAGGCCTATGACACCATGCCTGGCTAGTTTTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170565363 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17734665 9187 RMVar_ID_9187 Human_SNP_ID_5196019 A-to-I Human chr1 + 19264800 19264800 19264800 TCGCCCAGGCTGGAGTGCAGTGGCATGATCTCAGCTCACTGCAAGCTCCACCTCCCGGATTTACG TCGCCCAGGCTGGAGTGCAGTGGCATGATCTCGGCTCACTGCAAGCTCCACCTCCCGGATTTACG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559857383 Functional Loss SNV dbSNP153 33..33 33 - - - 9188 RMVar_ID_9188 Human_SNP_ID_5203589 A-to-I Human chr1 - 19292622 19292622 19292622 GGCTCACTGGAACCTCTGCCTCCTGGGTTCAAACGTTTCTCCTTGCCTCAGCCTTCCAAGTAACT GGCTCACTGGAACCTCTGCCTCCTGGGTTCAAGCGTTTCTCCTTGCCTCAGCCTTCCAAGTAACT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1160939848 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_129821 9189 RMVar_ID_9189 Human_SNP_ID_5203808 A-to-I Human chr1 - 19293624 19293624 19293624 GTCTTGAACTCCTAGGCTCAAGCAATCCGCCCATCTTGTCCTCCCAAAGTCTGGGATTATAGGCA GTCTTGAACTCCTAGGCTCAAGCAATCCGCCCGTCTTGTCCTCCCAAAGTCTGGGATTATAGGCA T C LOC100506730 RNACentral:URS000075DFBF lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232661041 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_129821 9190 RMVar_ID_9190 Human_SNP_ID_5203994 A-to-I Human chr1 - 19294235 19294233 19294235 TTATTTTTATTTATTTATTTTTTTTGAGACAGAGTCTCGCTCTGTTGTCCAGGCTGGAATGCAGT TTATTTTTATTTATTTATTTTTTTTGAGACAG__TCTCGCTCTGTTGTCCAGGCTGGAATGCAGT ACT A LOC100506730,LOC100506730:2 RNACentral:URS0000D5B67B,RNACentral:URS000075DFBF lincRNA,lincRNA exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1166375782 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_129821 9191 RMVar_ID_9191 Human_SNP_ID_5203995 A-to-I Human chr1 - 19294235 19294235 19294235 TTATTTTTATTTATTTATTTTTTTTGAGACAGAGTCTCGCTCTGTTGTCCAGGCTGGAATGCAGT TTATTTTTATTTATTTATTTTTTTTGAGACAGTGTCTCGCTCTGTTGTCCAGGCTGGAATGCAGT T A LOC100506730,LOC100506730:2 RNACentral:URS0000D5B67B,RNACentral:URS000075DFBF lincRNA,lincRNA exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1372158041 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_129821 9192 RMVar_ID_9192 Human_SNP_ID_5205312 A-to-I Human chr1 - 19299783 19299783 19299783 CAATATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCCGGGCGAGGTAACAGGTGCCT CAATATGGTGAAACCCCGTCTCTACTAAAAATGCAAAAATTAGCCGGGCGAGGTAACAGGTGCCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170858292 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_129821 9193 RMVar_ID_9193 Human_SNP_ID_5205823 A-to-I Human chr1 - 19301782 19301782 19301782 GAGAGGCAGAGGTGGGAGGATCTCTTGGGCCCAGGAGGTGGAGGCTGCAGTGAGCCAAAATCAGA GAGAGGCAGAGGTGGGAGGATCTCTTGGGCCCCGGAGGTGGAGGCTGCAGTGAGCCAAAATCAGA T G - - Other Unknown GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs572551822 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_129821 9194 RMVar_ID_9194 Human_SNP_ID_5206592 A-to-I Human chr1 - 19304933 19304932 19304934 TAACGTAGCCTGCTTTTTAATTTTTTTGAGACAGAGTCTCACTCTGTTACCCAGGCGGTAGAACA TAACGTAGCCTGCTTTTTAATTTTTTTGAGA__GAGTCTCACTCTGTTACCCAGGCGGTAGAACA CTG C AKR7A2 Ensembl:ENSG00000053371 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1477920893 Functional Loss DEL dbSNP153 32..33 33 - - - 9195 RMVar_ID_9195 Human_SNP_ID_5210958 A-to-I Human chr1 + 19319792 19319792 19319792 GGGTGTGGTGGCGCGTGCCTGTGGTCCCAGCTACTCGGGAGGCTGAGGCAGGGGAATTGCTTGAG GGGTGTGGTGGCGCGTGCCTGTGGTCCCAGCTGCTCGGGAGGCTGAGGCAGGGGAATTGCTTGAG A G SLC66A1 Ensembl:ENSG00000040487 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1274094260 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_129823,RMVar_hsa_circ_108389 9196 RMVar_ID_9196 Human_SNP_ID_5213993 A-to-I Human chr1 + 19329163 19329163 19329163 TCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAACTGTTTGAACCTGGGAGACAGAGGTT TCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCGGGAGAACTGTTTGAACCTGGGAGACAGAGGTT A G SLC66A1 Ensembl:ENSG00000040487 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs923606833 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_129823,RMVar_hsa_circ_108389 9197 RMVar_ID_9197 Human_SNP_ID_5283441 A-to-I Human chr1 + 19599156 19599156 19599156 CGGCTCACTGCAACTTCTGTCTCCTTGGGCTCAAGTGATCCTCCCACCTCAGCCTCCTGAGTAGC CGGCTCACTGCAACTTCTGTCTCCTTGGGCTCGAGTGATCCTCCCACCTCAGCCTCCTGAGTAGC A G NBL1,MICOS10-NBL1,MICOS10 Ensembl:ENSG00000158747,Ensembl:ENSG00000270136,Ensembl:ENSG00000173436 Protein coding,Protein coding,Protein coding intron,intron,intron GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-Seq:(High) rs1056287203 Functional Loss SNV dbSNP153 33..33 33 - - - 9198 RMVar_ID_9198 Human_SNP_ID_5283799 A-to-I Human chr1 + 19600731 19600731 19600731 TCAGGTGATCCTCCCACCTCAGCCTCCTGAGTAGCTGGGACTGTGGGTACGCACCACCATACCCA TCAGGTGATCCTCCCACCTCAGCCTCCTGAGTGGCTGGGACTGTGGGTACGCACCACCATACCCA A G NBL1,MICOS10-NBL1,MICOS10 Ensembl:ENSG00000158747,Ensembl:ENSG00000270136,Ensembl:ENSG00000173436 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1352253366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10719023 9199 RMVar_ID_9199 Human_SNP_ID_5285104 A-to-I Human chr1 + 19606625 19606625 19606625 AAAATTGGCTGAGTGTGGTGGCGCATGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA AAAATTGGCTGAGTGTGGTGGCGCATGCCTGTGATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA A G NBL1,MICOS10-NBL1,MICOS10 Ensembl:ENSG00000158747,Ensembl:ENSG00000270136,Ensembl:ENSG00000173436 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs969108993 Functional Loss SNV dbSNP153 33..33 33 - - - 9200 RMVar_ID_9200 Human_SNP_ID_5285559 A-to-I Human chr1 - 19608385 19608385 19608385 CTCCTGTGGCCCGGAGTTGGATGTGTAGGGCAATGATACCCAGCTCCTTGCACCTCTGGGCCACA CTCCTGTGGCCCGGAGTTGGATGTGTAGGGCAGTGATACCCAGCTCCTTGCACCTCTGGGCCACA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs779101275 Functional Loss SNV dbSNP153 33..33 33 - - - 9201 RMVar_ID_9201 Human_SNP_ID_5285581 A-to-I Human chr1 - 19608436 19608436 19608436 GGGCTCTGAGGGCCGACTGGGCCCCAGGTCCAAGGGTCTTGGTCCTATTTCCTCCTGTGGCCCGG GGGCTCTGAGGGCCGACTGGGCCCCAGGTCCAGGGGTCTTGGTCCTATTTCCTCCTGTGGCCCGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs773953063 Functional Loss SNV dbSNP153 33..33 33 - - - 9202 RMVar_ID_9202 Human_SNP_ID_5290356 A-to-I Human chr1 + 19628224 19628224 19628224 CCTCAGCCTCCCGAGTAGCTGGGATTACAGGCATGCGCCATCACACCTGGCTAATTTTGTATTTT CCTCAGCCTCCCGAGTAGCTGGGATTACAGGCGTGCGCCATCACACCTGGCTAATTTTGTATTTT A G NBL1,MICOS10-NBL1,MICOS10 Ensembl:ENSG00000158747,Ensembl:ENSG00000270136,Ensembl:ENSG00000173436 Protein coding,Protein coding,Protein coding intron,intron,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs149551422 Functional Loss SNV dbSNP153 33..33 33 - - - 9203 RMVar_ID_9203 Human_SNP_ID_5290439 A-to-I Human chr1 + 19628571 19628571 19628571 GGGCATGGTGGCGCACACCTGTAGTCCCAGCTACTCAGGAGGTTGAGGCAGGAGAATCATTTGAA GGGCATGGTGGCGCACACCTGTAGTCCCAGCTGCTCAGGAGGTTGAGGCAGGAGAATCATTTGAA A G NBL1,MICOS10-NBL1,MICOS10 Ensembl:ENSG00000158747,Ensembl:ENSG00000270136,Ensembl:ENSG00000173436 Protein coding,Protein coding,Protein coding intron,intron,3'UTR GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs983248741 Functional Loss SNV dbSNP153 33..33 33 - - - 9204 RMVar_ID_9204 Human_SNP_ID_5321830 A-to-I Human chr1 - 19751823 19751823 19751823 AGGATGGTCTCGATCTCCTGACCTCGTGATCCACCCGCCTTGGCCTCCCAAAGTGCTGGGACCAC AGGATGGTCTCGATCTCCTGACCTCGTGATCCGCCCGCCTTGGCCTCCCAAAGTGCTGGGACCAC T C TMCO4 Ensembl:ENSG00000162542 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs969948250 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_347308,RMVar_hsa_circ_306610,RMVar_hsa_circ_55796,RMVar_hsa_circ_68802,RMVar_hsa_circ_129837,RMVar_hsa_circ_129838,RMVar_hsa_circ_71772,RMVar_hsa_circ_52963 9205 RMVar_ID_9205 Human_SNP_ID_5323887 A-to-I Human chr1 - 19760480 19760480 19760480 CCAGGAGGTTGAGGCTGCAGTGAGCCAAGATCATACCACTGCACTCCATCCTGGGTGACAGTGAG CCAGGAGGTTGAGGCTGCAGTGAGCCAAGATCGTACCACTGCACTCCATCCTGGGTGACAGTGAG T C TMCO4 Ensembl:ENSG00000162542 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1266141062 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24622278 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 9206 RMVar_ID_9206 Human_SNP_ID_5544314 A-to-I Human chr1 - 20646030 20646030 20646030 TGGCCTCAAGCAATCCTCAAGCAAGCCTCCCAAAGTGTTGGGATTACAGGTGTCAGCCACTGTGC TGGCCTCAAGCAATCCTCAAGCAAGCCTCCCAGAGTGTTGGGATTACAGGTGTCAGCCACTGTGC T C PINK1-AS Ensembl:ENSG00000117242 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1254689916 Functional Loss SNV dbSNP153 33..33 33 - - - 9207 RMVar_ID_9207 Human_SNP_ID_5544378 A-to-I Human chr1 - 20646244 20646244 20646244 CTGCCCAGGCTGGAGTACAGTGGCACATTCATAGCTCATTGCAGACTCTTAACTCCTAGGCTCAA CTGCCCAGGCTGGAGTACAGTGGCACATTCATTGCTCATTGCAGACTCTTAACTCCTAGGCTCAA T A PINK1-AS Ensembl:ENSG00000117242 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs746545227 Functional Loss SNV dbSNP153 33..33 33 - - - 9208 RMVar_ID_9208 Human_SNP_ID_5544876 A-to-I Human chr1 - 20647945 20647945 20647945 TAGCCAGGCATGGTGGTGTGTGCCTGTATCCCAGCTACTCGGGAGGCTGAGACAGGAGAATTACT TAGCCAGGCATGGTGGTGTGTGCCTGTATCCCCGCTACTCGGGAGGCTGAGACAGGAGAATTACT T G PINK1-AS Ensembl:ENSG00000117242 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1405754817 Functional Loss SNV dbSNP153 33..33 33 - - - 9209 RMVar_ID_9209 Human_SNP_ID_5545415 A-to-I Human chr1 - 20649665 20649663 20649665 TGCCTCCAGGGTTCAAACGATTCTCCTGCTTCAGCCTCCCGAGTACCTGGAATTACAGGCGTGTG TGCCTCCAGGGTTCAAACGATTCTCCTGCTTC__CCTCCCGAGTACCTGGAATTACAGGCGTGTG GCT G PINK1-AS Ensembl:ENSG00000117242 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs148288214 Functional Loss DEL dbSNP153 33..34 33 - - - 9210 RMVar_ID_9210 Human_SNP_ID_5546276 A-to-I Human chr1 - 20651958 20651958 20651958 AGCTGGGCGTGGTGGTGGGCACCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAAAGGCA AGCTGGGCGTGGTGGTGGGCACCTGTAGTCCCGGCTACTCGGGAGGCTGAGGCAGGAGAAAGGCA T C PINK1-AS,DDOST Ensembl:ENSG00000117242,Ensembl:ENSG00000244038 lincRNA,Protein coding exon,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1131984 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_339840,Human_RBP_ID_5109015,Human_RBP_ID_5136109 9211 RMVar_ID_9211 Human_SNP_ID_5546277 A-to-I Human chr1 - 20651964 20651964 20651964 AAAATTAGCTGGGCGTGGTGGTGGGCACCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTAGCTGGGCGTGGTGGTGGGCACCTGTGGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA T C PINK1-AS,DDOST Ensembl:ENSG00000117242,Ensembl:ENSG00000244038 lincRNA,Protein coding exon,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1131982 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_339840,Human_RBP_ID_5109015,Human_RBP_ID_5136109 9212 RMVar_ID_9212 Human_SNP_ID_5546302 A-to-I Human chr1 - 20652030 20652030 20652030 ACGAGGTCAGGAGATCGAGACTATCCTGGCTAACACGGTAAAACCCTGTCTCTACTAAAAGTACA ACGAGGTCAGGAGATCGAGACTATCCTGGCTAGCACGGTAAAACCCTGTCTCTACTAAAAGTACA T C PINK1-AS,DDOST Ensembl:ENSG00000117242,Ensembl:ENSG00000244038 lincRNA,Protein coding exon,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs3192302 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_339841 Human_miRNA_ID_3165991 9213 RMVar_ID_9213 Human_SNP_ID_5546314 A-to-I Human chr1 - 20652071 20652071 20652071 CCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGCGGCTCACGAGGTCAGGAGATCGAGACTAT CCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGGCTCACGAGGTCAGGAGATCGAGACTAT T C PINK1-AS,DDOST Ensembl:ENSG00000117242,Ensembl:ENSG00000244038 lincRNA,Protein coding exon,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1131967 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_339843,Human_RBP_ID_8962060 Human_miRNA_ID_3209534 9214 RMVar_ID_9214 Human_SNP_ID_5546453 A-to-I Human chr1 - 20652473 20652473 20652473 CACGCAGTATGAGCGCTTCATCCCCTCGGCCTACCCCTACTACGCCAGCGCCTTCTCCATGATGC CACGCAGTATGAGCGCTTCATCCCCTCGGCCTGCCCCTACTACGCCAGCGCCTTCTCCATGATGC T C DDOST Ensembl:ENSG00000244038 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs749823019 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224840,Human_RBP_ID_339855,Human_RBP_ID_746816,Human_RBP_ID_974434,Human_RBP_ID_1346357,Human_RBP_ID_3293998,Human_RBP_ID_5746278,Human_RBP_ID_17215305,Human_RBP_ID_17449202,Human_RBP_ID_17646898,Human_RBP_ID_17736975,Human_RBP_ID_22428173,Human_RBP_ID_22749857,Human_RBP_ID_23205745,Human_RBP_ID_23359652,Human_RBP_ID_24449821,Human_RBP_ID_27393385,Human_RBP_ID_27585695 Human_Splice_Rec_26456,Human_Splice_Rec_26476,Human_Splice_Rec_26496 9215 RMVar_ID_9215 Human_SNP_ID_5546454 A-to-I Human chr1 - 20652473 20652473 20652473 CACGCAGTATGAGCGCTTCATCCCCTCGGCCTACCCCTACTACGCCAGCGCCTTCTCCATGATGC CACGCAGTATGAGCGCTTCATCCCCTCGGCCTCCCCCTACTACGCCAGCGCCTTCTCCATGATGC T G DDOST Ensembl:ENSG00000244038 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs749823019 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224840,Human_RBP_ID_339855,Human_RBP_ID_746816,Human_RBP_ID_974434,Human_RBP_ID_1346357,Human_RBP_ID_3293998,Human_RBP_ID_5746278,Human_RBP_ID_17215305,Human_RBP_ID_17449202,Human_RBP_ID_17646898,Human_RBP_ID_17736975,Human_RBP_ID_22428173,Human_RBP_ID_22749857,Human_RBP_ID_23205745,Human_RBP_ID_23359652,Human_RBP_ID_24449821,Human_RBP_ID_27393385,Human_RBP_ID_27585695 Human_Splice_Rec_26456,Human_Splice_Rec_26476,Human_Splice_Rec_26496 9216 RMVar_ID_9216 Human_SNP_ID_5550944 A-to-I Human chr1 - 20667997 20667997 20667997 CACCTCTTTTTTTTTTTTTGAGACAGAGTTTCACTCTTGTTGCCCAGGCTGGAGTGCAGTTGTGC CACCTCTTTTTTTTTTTTTGAGACAGAGTTTCGCTCTTGTTGCCCAGGCTGGAGTGCAGTTGTGC T C KIF17 Ensembl:ENSG00000117245 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1193450913 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19392 9217 RMVar_ID_9217 Human_SNP_ID_5574446 A-to-I Human chr1 - 20750416 20750416 20750416 TCAAGTGACTCTCCTGCCTCAGCCTCCCAAGTAGCTGAGACCACAGGCACCTGCCACACCTGGCT TCAAGTGACTCTCCTGCCTCAGCCTCCCAAGTGGCTGAGACCACAGGCACCTGCCACACCTGGCT T C HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1006770766 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10748824,Human_RBP_ID_23359919 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_34502,RMVar_hsa_circ_129887,RMVar_hsa_circ_129888 9218 RMVar_ID_9218 Human_SNP_ID_5574468 A-to-I Human chr1 - 20750489 20750489 20750489 AGAATCTTACTCTGTCGCCGAGGCTGGAGTTCAGTGGCATGATTTCGGCACACTGCAACCCCGCG AGAATCTTACTCTGTCGCCGAGGCTGGAGTTCGGTGGCATGATTTCGGCACACTGCAACCCCGCG T C HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs986246148 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5747138,Human_RBP_ID_10748830,Human_RBP_ID_23359922 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_34502,RMVar_hsa_circ_129887,RMVar_hsa_circ_129888 9219 RMVar_ID_9219 Human_SNP_ID_5574797 A-to-I Human chr1 - 20751504 20751504 20751504 CCGAGGTTGGTCTTGAACTCTTGGCCTCAAGCAGTCCTCCCCCATTAGCCTCCCAAAGTACTGGG CCGAGGTTGGTCTTGAACTCTTGGCCTCAAGCGGTCCTCCCCCATTAGCCTCCCAAAGTACTGGG T C HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs905963634 Functional Loss SNV dbSNP153 33..33 33 - - - 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_34502,RMVar_hsa_circ_129887,RMVar_hsa_circ_129888 9220 RMVar_ID_9220 Human_SNP_ID_5574810 A-to-I Human chr1 - 20751553 20751549 20751553 TCATAGCTAGTTTTTTTATTTTTAGTAGAGAGAGAGTCTCACTATGTTGCCGAGGTTGGTCTTGA TCATAGCTAGTTTTTTTATTTTTAGTAGAGAG____TCTCACTATGTTGCCGAGGTTGGTCTTGA ACTCT A HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs753448929 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_5747151 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_34502,RMVar_hsa_circ_129887,RMVar_hsa_circ_129888 9221 RMVar_ID_9221 Human_SNP_ID_5574811 A-to-I Human chr1 - 20751553 20751549 20751553 TCATAGCTAGTTTTTTTATTTTTAGTAGAGAGAGAGTCTCACTATGTTGCCGAGGTTGGTCTTGA TCATAGCTAGTTTTTTTATTTTTAGTAGAGAG__AGTCTCACTATGTTGCCGAGGTTGGTCTTGA ACTCT ACT HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs753448929 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_5747151 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_34502,RMVar_hsa_circ_129887,RMVar_hsa_circ_129888 9222 RMVar_ID_9222 Human_SNP_ID_5574843 A-to-I Human chr1 - 20751671 20751671 20751671 TCACTCAGGCTGGAGTATAGTGATGTAATCATAGCTCACTAATAGCCTCAACTTCCTGGGCTTAA TCACTCAGGCTGGAGTATAGTGATGTAATCATGGCTCACTAATAGCCTCAACTTCCTGGGCTTAA T C HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1137047 Functional Loss SNV dbSNP153 33..33 33 - - - 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_34502,RMVar_hsa_circ_129887,RMVar_hsa_circ_129888 9223 RMVar_ID_9223 Human_SNP_ID_5575854 A-to-I Human chr1 - 20755311 20755311 20755311 TGCCTGCCTCAGCTTCCCAAAGTGTTGGAATTACAGGTGTGATCCACCACACCTGACCAGGGCTC TGCCTGCCTCAGCTTCCCAAAGTGTTGGAATTGCAGGTGTGATCCACCACACCTGACCAGGGCTC T C HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,29796672,31158229,31158229,31158229 RNA-Seq:(High) rs907735520 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17449274,Human_RBP_ID_17557009,Human_RBP_ID_19263281,Human_RBP_ID_24628335 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_121886,RMVar_hsa_circ_34502,RMVar_hsa_circ_129887,RMVar_hsa_circ_129888,RMVar_hsa_circ_89876,RMVar_hsa_circ_120042,RMVar_hsa_circ_129890,RMVar_hsa_circ_129891 9224 RMVar_ID_9224 Human_SNP_ID_5575892 A-to-I Human chr1 - 20755406 20755406 20755406 CACCATGCCTGATTAATTTTTGTATTTTTTGTAGAAATGGGGTTTCGCCGTGTTGCCCAGGCTAC CACCATGCCTGATTAATTTTTGTATTTTTTGTGGAAATGGGGTTTCGCCGTGTTGCCCAGGCTAC T C HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE38233;GSE100210;GSE112787;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;293 Flip-In T-REx cells,empty vector;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,29967493,31158229 RNA-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 9225 RMVar_ID_9225 Human_SNP_ID_5575913 A-to-I Human chr1 - 20755453 20755453 20755453 CTCCCATCTTAGCCTCCCTAATAGCTGGGATTATAGGCGTGCACCACCACCATGCCTGATTAATT CTCCCATCTTAGCCTCCCTAATAGCTGGGATTGTAGGCGTGCACCACCACCATGCCTGATTAATT T C HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs547068037 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24628340 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 9226 RMVar_ID_9226 Human_SNP_ID_5575916 A-to-I Human chr1 - 20755488 20755488 20755488 TCACTGCAACCTCCACCTCCCTGGCTCAAGCAATCCTCCCATCTTAGCCTCCCTAATAGCTGGGA TCACTGCAACCTCCACCTCCCTGGCTCAAGCAGTCCTCCCATCTTAGCCTCCCTAATAGCTGGGA T C HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1180259328 Functional Loss SNV dbSNP153 33..33 33 - - - 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 9227 RMVar_ID_9227 Human_SNP_ID_5576190 A-to-I Human chr1 - 20756518 20756518 20756518 TTTCCCAGGCTGGAGTGCAGTGGCACAATCACAGCTCACTGTAGCCTCTATCTCCCAGGTTCAAG TTTCCCAGGCTGGAGTGCAGTGGCACAATCACTGCTCACTGTAGCCTCTATCTCCCAGGTTCAAG T A HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1282574262 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10749032 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 9228 RMVar_ID_9228 Human_SNP_ID_5576192 A-to-I Human chr1 - 20756523 20756523 20756523 CTCTGTTTCCCAGGCTGGAGTGCAGTGGCACAATCACAGCTCACTGTAGCCTCTATCTCCCAGGT CTCTGTTTCCCAGGCTGGAGTGCAGTGGCACAGTCACAGCTCACTGTAGCCTCTATCTCCCAGGT T C HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1484173384 Functional Loss SNV dbSNP153 33..33 33 - - - 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 9229 RMVar_ID_9229 Human_SNP_ID_5576256 A-to-I Human chr1 - 20756758 20756758 20756758 TGAGCCAAGATTGCACCACTGTGCTCTAGGCTAGGTGACAGAGCGAGATGCCATCTCAAACAAAC TGAGCCAAGATTGCACCACTGTGCTCTAGGCTGGGTGACAGAGCGAGATGCCATCTCAAACAAAC T C HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE38233;GSE100210;GSE112787;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;293 Flip-In T-REx cells,empty vector;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,29967493,31158229,31158229 RNA-Seq:(High) rs1472219848 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1252510 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 9230 RMVar_ID_9230 Human_SNP_ID_5576261 A-to-I Human chr1 - 20756783 20756783 20756783 TGAACGCGGGAGGTGGAGGTTGCATTGAGCCAAGATTGCACCACTGTGCTCTAGGCTAGGTGACA TGAACGCGGGAGGTGGAGGTTGCATTGAGCCAGGATTGCACCACTGTGCTCTAGGCTAGGTGACA T C HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229,31158229 RNA-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 9231 RMVar_ID_9231 Human_SNP_ID_5576322 A-to-I Human chr1 - 20756991 20756991 20756991 AAATTAACATTGAGGTCTGGGTGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTAAG AAATTAACATTGAGGTCTGGGTGCGGTGGCTCCCACCTGTAATCCCAGCACTTTGGGAGGCTAAG T G HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs943355672 Functional Loss SNV dbSNP153 33..33 33 - - - 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 9232 RMVar_ID_9232 Human_SNP_ID_5576650 A-to-I Human chr1 - 20757961 20757961 20757961 TTTTGTATTTTTAGTAGAGCTGAGGTTTCACTATGTTGGCCAGGCTGGTCTCGAACTCCTGATCT TTTTGTATTTTTAGTAGAGCTGAGGTTTCACTGTGTTGGCCAGGCTGGTCTCGAACTCCTGATCT T C HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs577777425 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41282,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_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,RMVar_hsa_circ_129894,RMVar_hsa_circ_129898,RMVar_hsa_circ_277441,RMVar_hsa_circ_279099,RMVar_hsa_circ_324727,RMVar_hsa_circ_332930,RMVar_hsa_circ_309625,RMVar_hsa_circ_278114,RMVar_hsa_circ_273252,RMVar_hsa_circ_129896,RMVar_hsa_circ_129897,RMVar_hsa_circ_129895,RMVar_hsa_circ_129892,RMVar_hsa_circ_129893 9233 RMVar_ID_9233 Human_SNP_ID_5576696 A-to-I Human chr1 - 20758107 20758107 20758107 GAGTCTTGCTCCGTTGCCTAGGTTGGATTGCAATGGCATGGTCTCAGCTCACTGCAACCTCCGCC GAGTCTTGCTCCGTTGCCTAGGTTGGATTGCAGTGGCATGGTCTCAGCTCACTGCAACCTCCGCC T C HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1295406367 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41282,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_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,RMVar_hsa_circ_129894,RMVar_hsa_circ_129898,RMVar_hsa_circ_277441,RMVar_hsa_circ_279099,RMVar_hsa_circ_324727,RMVar_hsa_circ_332930,RMVar_hsa_circ_309625,RMVar_hsa_circ_278114,RMVar_hsa_circ_273252,RMVar_hsa_circ_129896,RMVar_hsa_circ_129897,RMVar_hsa_circ_129895,RMVar_hsa_circ_129892,RMVar_hsa_circ_129893 9234 RMVar_ID_9234 Human_SNP_ID_5576795 A-to-I Human chr1 - 20758422 20758422 20758422 GAATCACTTGAACCTGAGGGGGCGGAGGTTGCAGTGACCTGAGATCGCGCCACTGCACTCCAGCC GAATCACTTGAACCTGAGGGGGCGGAGGTTGCGGTGACCTGAGATCGCGCCACTGCACTCCAGCC T C HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1010324285 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24628389 RMVar_hsa_circ_41282,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_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,RMVar_hsa_circ_129894,RMVar_hsa_circ_129898,RMVar_hsa_circ_277441,RMVar_hsa_circ_279099,RMVar_hsa_circ_324727,RMVar_hsa_circ_332930,RMVar_hsa_circ_309625,RMVar_hsa_circ_278114,RMVar_hsa_circ_273252,RMVar_hsa_circ_129896,RMVar_hsa_circ_129897,RMVar_hsa_circ_129895,RMVar_hsa_circ_129892,RMVar_hsa_circ_129893 9235 RMVar_ID_9235 Human_SNP_ID_5576836 A-to-I Human chr1 - 20758547 20758547 20758547 GGTCGGAAGATCAAGACCATCCTTGCTAACACAGTGAAACCCCGTCTTTACTAAAAGTACAAAAA GGTCGGAAGATCAAGACCATCCTTGCTAACACGGTGAAACCCCGTCTTTACTAAAAGTACAAAAA T C HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs975098749 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41282,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_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,RMVar_hsa_circ_129894,RMVar_hsa_circ_129898,RMVar_hsa_circ_277441,RMVar_hsa_circ_279099,RMVar_hsa_circ_324727,RMVar_hsa_circ_332930,RMVar_hsa_circ_309625,RMVar_hsa_circ_278114,RMVar_hsa_circ_273252,RMVar_hsa_circ_129896,RMVar_hsa_circ_129897,RMVar_hsa_circ_129895,RMVar_hsa_circ_129892,RMVar_hsa_circ_129893 9236 RMVar_ID_9236 Human_SNP_ID_5576904 A-to-I Human chr1 - 20758722 20758722 20758722 AGGGTTGCTTGAGCCTGGGAGATCAAGGCTACAGTGAGCCATGGTCATACCACTGCACTCCATCC AGGGTTGCTTGAGCCTGGGAGATCAAGGCTACGGTGAGCCATGGTCATACCACTGCACTCCATCC T C HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1399695000 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41282,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_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,RMVar_hsa_circ_129894,RMVar_hsa_circ_129898,RMVar_hsa_circ_277441,RMVar_hsa_circ_279099,RMVar_hsa_circ_324727,RMVar_hsa_circ_332930,RMVar_hsa_circ_309625,RMVar_hsa_circ_278114,RMVar_hsa_circ_273252,RMVar_hsa_circ_129896,RMVar_hsa_circ_129897,RMVar_hsa_circ_129895,RMVar_hsa_circ_129892,RMVar_hsa_circ_129893 9237 RMVar_ID_9237 Human_SNP_ID_5577042 A-to-I Human chr1 - 20759189 20759189 20759189 TCCATGTTGGTCAAGCTGGTGTCAAACTCCCAACCTCAGGTGATCTGCCGGCCTCGGCCCCCCAG TCCATGTTGGTCAAGCTGGTGTCAAACTCCCAGCCTCAGGTGATCTGCCGGCCTCGGCCCCCCAG T C HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs772298587 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41282,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_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,RMVar_hsa_circ_129894,RMVar_hsa_circ_129898,RMVar_hsa_circ_277441,RMVar_hsa_circ_279099,RMVar_hsa_circ_324727,RMVar_hsa_circ_332930,RMVar_hsa_circ_309625,RMVar_hsa_circ_278114,RMVar_hsa_circ_273252,RMVar_hsa_circ_129896,RMVar_hsa_circ_129897,RMVar_hsa_circ_129895,RMVar_hsa_circ_129892,RMVar_hsa_circ_129893 9238 RMVar_ID_9238 Human_SNP_ID_5577055 A-to-I Human chr1 - 20759218 20759218 20759218 TTTTGTATTTTTAGTACAAATGGGGTTTCTCCATGTTGGTCAAGCTGGTGTCAAACTCCCAACCT TTTTGTATTTTTAGTACAAATGGGGTTTCTCCTTGTTGGTCAAGCTGGTGTCAAACTCCCAACCT T A HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1035810217 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41282,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_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,RMVar_hsa_circ_129894,RMVar_hsa_circ_129898,RMVar_hsa_circ_277441,RMVar_hsa_circ_279099,RMVar_hsa_circ_324727,RMVar_hsa_circ_332930,RMVar_hsa_circ_309625,RMVar_hsa_circ_278114,RMVar_hsa_circ_273252,RMVar_hsa_circ_129896,RMVar_hsa_circ_129897,RMVar_hsa_circ_129895,RMVar_hsa_circ_129892,RMVar_hsa_circ_129893 9239 RMVar_ID_9239 Human_SNP_ID_5577056 A-to-I Human chr1 - 20759218 20759218 20759218 TTTTGTATTTTTAGTACAAATGGGGTTTCTCCATGTTGGTCAAGCTGGTGTCAAACTCCCAACCT TTTTGTATTTTTAGTACAAATGGGGTTTCTCCGTGTTGGTCAAGCTGGTGTCAAACTCCCAACCT T C HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1035810217 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41282,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_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,RMVar_hsa_circ_129894,RMVar_hsa_circ_129898,RMVar_hsa_circ_277441,RMVar_hsa_circ_279099,RMVar_hsa_circ_324727,RMVar_hsa_circ_332930,RMVar_hsa_circ_309625,RMVar_hsa_circ_278114,RMVar_hsa_circ_273252,RMVar_hsa_circ_129896,RMVar_hsa_circ_129897,RMVar_hsa_circ_129895,RMVar_hsa_circ_129892,RMVar_hsa_circ_129893 9240 RMVar_ID_9240 Human_SNP_ID_5577484 A-to-I Human chr1 - 20760674 20760674 20760674 TGCCACCACACCCGGGTAATTTTTGTATTTTTAGTAGAGACAGAGTTTCACCATGTTGGCCAGGC TGCCACCACACCCGGGTAATTTTTGTATTTTTGGTAGAGACAGAGTTTCACCATGTTGGCCAGGC T C HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs561745106 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41282,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_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,RMVar_hsa_circ_129894,RMVar_hsa_circ_129898,RMVar_hsa_circ_277441,RMVar_hsa_circ_279099,RMVar_hsa_circ_324727,RMVar_hsa_circ_332930,RMVar_hsa_circ_309625,RMVar_hsa_circ_278114,RMVar_hsa_circ_273252,RMVar_hsa_circ_129896,RMVar_hsa_circ_129897,RMVar_hsa_circ_129895,RMVar_hsa_circ_129892,RMVar_hsa_circ_129893 9241 RMVar_ID_9241 Human_SNP_ID_5577503 A-to-I Human chr1 - 20760736 20760736 20760736 CGCCTCCTCGGTTCAAGCGATTTTCCTGTCTCAGCCTCCCGAGTAGCTGGGATTACAGGCTGTGC CGCCTCCTCGGTTCAAGCGATTTTCCTGTCTCCGCCTCCCGAGTAGCTGGGATTACAGGCTGTGC T G HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1171473523 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41282,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_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,RMVar_hsa_circ_129894,RMVar_hsa_circ_129898,RMVar_hsa_circ_277441,RMVar_hsa_circ_279099,RMVar_hsa_circ_324727,RMVar_hsa_circ_332930,RMVar_hsa_circ_309625,RMVar_hsa_circ_278114,RMVar_hsa_circ_273252,RMVar_hsa_circ_129896,RMVar_hsa_circ_129897,RMVar_hsa_circ_129895,RMVar_hsa_circ_129892,RMVar_hsa_circ_129893 9242 RMVar_ID_9242 Human_SNP_ID_5577509 A-to-I Human chr1 - 20760753 20760753 20760753 CGGCTCACTGCAACCTCCGCCTCCTCGGTTCAAGCGATTTTCCTGTCTCAGCCTCCCGAGTAGCT CGGCTCACTGCAACCTCCGCCTCCTCGGTTCAGGCGATTTTCCTGTCTCAGCCTCCCGAGTAGCT T C HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1292412267 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41282,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_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,RMVar_hsa_circ_129894,RMVar_hsa_circ_129898,RMVar_hsa_circ_277441,RMVar_hsa_circ_279099,RMVar_hsa_circ_324727,RMVar_hsa_circ_332930,RMVar_hsa_circ_309625,RMVar_hsa_circ_278114,RMVar_hsa_circ_273252,RMVar_hsa_circ_129896,RMVar_hsa_circ_129897,RMVar_hsa_circ_129895,RMVar_hsa_circ_129892,RMVar_hsa_circ_129893 9243 RMVar_ID_9243 Human_SNP_ID_5577620 A-to-I Human chr1 - 20761155 20761155 20761155 CTGTAGTTCCAGCTACTCAAGAGGCCAAGGCAAGAGAATCACTTAAACCTGGGAGGCATAGTCTG CTGTAGTTCCAGCTACTCAAGAGGCCAAGGCAGGAGAATCACTTAAACCTGGGAGGCATAGTCTG T C HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1414322946 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41282,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_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,RMVar_hsa_circ_129894,RMVar_hsa_circ_129898,RMVar_hsa_circ_277441,RMVar_hsa_circ_279099,RMVar_hsa_circ_324727,RMVar_hsa_circ_332930,RMVar_hsa_circ_309625,RMVar_hsa_circ_278114,RMVar_hsa_circ_273252,RMVar_hsa_circ_129896,RMVar_hsa_circ_129897,RMVar_hsa_circ_129895,RMVar_hsa_circ_129892,RMVar_hsa_circ_129893 9244 RMVar_ID_9244 Human_SNP_ID_5578476 A-to-I Human chr1 - 20764436 20764436 20764436 AGGAGGCTGAGGCAGGAGAATCGCTTGAACCCAGGAGGTGGAGTTCGCAGTGAGCCGAGATTGCG AGGAGGCTGAGGCAGGAGAATCGCTTGAACCCTGGAGGTGGAGTTCGCAGTGAGCCGAGATTGCG T A HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1416183907 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41282,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_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,RMVar_hsa_circ_129894,RMVar_hsa_circ_129898,RMVar_hsa_circ_277441,RMVar_hsa_circ_279099,RMVar_hsa_circ_324727,RMVar_hsa_circ_332930,RMVar_hsa_circ_309625,RMVar_hsa_circ_278114,RMVar_hsa_circ_273252,RMVar_hsa_circ_129896,RMVar_hsa_circ_129897,RMVar_hsa_circ_129895,RMVar_hsa_circ_129892,RMVar_hsa_circ_129893 9245 RMVar_ID_9245 Human_SNP_ID_5578484 A-to-I Human chr1 - 20764459 20764459 20764459 GGCATGTGCAGTCTCAGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACCCAGGAGGTGGA GGCATGTGCAGTCTCAGCTACTCAGGAGGCTGTGGCAGGAGAATCGCTTGAACCCAGGAGGTGGA T A HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335278392 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41282,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_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,RMVar_hsa_circ_129894,RMVar_hsa_circ_129898,RMVar_hsa_circ_277441,RMVar_hsa_circ_279099,RMVar_hsa_circ_324727,RMVar_hsa_circ_332930,RMVar_hsa_circ_309625,RMVar_hsa_circ_278114,RMVar_hsa_circ_273252,RMVar_hsa_circ_129896,RMVar_hsa_circ_129897,RMVar_hsa_circ_129895,RMVar_hsa_circ_129892,RMVar_hsa_circ_129893 9246 RMVar_ID_9246 Human_SNP_ID_5578602 A-to-I Human chr1 - 20764793 20764793 20764793 TCAGCTCACTGCAGCCTCTAACTCCCGGGTTCAAGCGATTTTCCTGCCACAGCCTCCGAATAGCT TCAGCTCACTGCAGCCTCTAACTCCCGGGTTCGAGCGATTTTCCTGCCACAGCCTCCGAATAGCT T C HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs575173726 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10749215 RMVar_hsa_circ_41282,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_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,RMVar_hsa_circ_129894,RMVar_hsa_circ_129898,RMVar_hsa_circ_277441,RMVar_hsa_circ_279099,RMVar_hsa_circ_324727,RMVar_hsa_circ_332930,RMVar_hsa_circ_309625,RMVar_hsa_circ_278114,RMVar_hsa_circ_273252,RMVar_hsa_circ_129896,RMVar_hsa_circ_129897,RMVar_hsa_circ_129895,RMVar_hsa_circ_129892,RMVar_hsa_circ_129893 9247 RMVar_ID_9247 Human_SNP_ID_5578618 A-to-I Human chr1 - 20764834 20764834 20764834 TCTTGCTCTTGTTACCCAGGCTGGAGTGCAATAGCGCAGTCTCAGCTCACTGCAGCCTCTAACTC TCTTGCTCTTGTTACCCAGGCTGGAGTGCAATGGCGCAGTCTCAGCTCACTGCAGCCTCTAACTC T C HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1391847770 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41282,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_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,RMVar_hsa_circ_129894,RMVar_hsa_circ_129898,RMVar_hsa_circ_277441,RMVar_hsa_circ_279099,RMVar_hsa_circ_324727,RMVar_hsa_circ_332930,RMVar_hsa_circ_309625,RMVar_hsa_circ_278114,RMVar_hsa_circ_273252,RMVar_hsa_circ_129896,RMVar_hsa_circ_129897,RMVar_hsa_circ_129895,RMVar_hsa_circ_129892,RMVar_hsa_circ_129893 9248 RMVar_ID_9248 Human_SNP_ID_5581196 A-to-I Human chr1 - 20774225 20774225 20774225 TGCTGGGATTACAGGCATGAGCCACTGCACCCAGCCTATCGTCTGTTGTTAAATGTTCTAATGCA TGCTGGGATTACAGGCATGAGCCACTGCACCCTGCCTATCGTCTGTTGTTAAATGTTCTAATGCA T A HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs207460052 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1734517,Human_RBP_ID_9481214,Human_RBP_ID_10749514,Human_RBP_ID_23360029,Human_RBP_ID_24628637 RMVar_hsa_circ_41282,RMVar_hsa_circ_129876,RMVar_hsa_circ_129880,RMVar_hsa_circ_265631,RMVar_hsa_circ_267873,RMVar_hsa_circ_129881,RMVar_hsa_circ_129879,RMVar_hsa_circ_335005,RMVar_hsa_circ_291851,RMVar_hsa_circ_129884,RMVar_hsa_circ_337821,RMVar_hsa_circ_129889,RMVar_hsa_circ_89876,RMVar_hsa_circ_129898,RMVar_hsa_circ_277441,RMVar_hsa_circ_278114,RMVar_hsa_circ_273252,RMVar_hsa_circ_129896,RMVar_hsa_circ_129897,RMVar_hsa_circ_129895,RMVar_hsa_circ_288326,RMVar_hsa_circ_291701,RMVar_hsa_circ_280308,RMVar_hsa_circ_95080,RMVar_hsa_circ_104519,RMVar_hsa_circ_129900,RMVar_hsa_circ_129902,RMVar_hsa_circ_129903,RMVar_hsa_circ_129901,RMVar_hsa_circ_129907,RMVar_hsa_circ_275156,RMVar_hsa_circ_316684,RMVar_hsa_circ_129899,RMVar_hsa_circ_357753,RMVar_hsa_circ_129908,RMVar_hsa_circ_307361,RMVar_hsa_circ_343338,RMVar_hsa_circ_329417,RMVar_hsa_circ_129911,RMVar_hsa_circ_129912,RMVar_hsa_circ_129913,RMVar_hsa_circ_30511,RMVar_hsa_circ_76618,RMVar_hsa_circ_357655,RMVar_hsa_circ_129914 9249 RMVar_ID_9249 Human_SNP_ID_5581207 A-to-I Human chr1 - 20774261 20774261 20774261 GGCCTCAAGCTGTCCTCCCTCCTCAGCCTCCTAAATTGCTGGGATTACAGGCATGAGCCACTGCA GGCCTCAAGCTGTCCTCCCTCCTCAGCCTCCTCAATTGCTGGGATTACAGGCATGAGCCACTGCA T G HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1052607213 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5641485,Human_RBP_ID_8296830,Human_RBP_ID_9481215,Human_RBP_ID_22873574,Human_RBP_ID_23146392,Human_RBP_ID_23360030,Human_RBP_ID_24756757 RMVar_hsa_circ_41282,RMVar_hsa_circ_129876,RMVar_hsa_circ_129880,RMVar_hsa_circ_265631,RMVar_hsa_circ_267873,RMVar_hsa_circ_129881,RMVar_hsa_circ_129879,RMVar_hsa_circ_335005,RMVar_hsa_circ_291851,RMVar_hsa_circ_129884,RMVar_hsa_circ_337821,RMVar_hsa_circ_129889,RMVar_hsa_circ_89876,RMVar_hsa_circ_129898,RMVar_hsa_circ_277441,RMVar_hsa_circ_278114,RMVar_hsa_circ_273252,RMVar_hsa_circ_129896,RMVar_hsa_circ_129897,RMVar_hsa_circ_129895,RMVar_hsa_circ_288326,RMVar_hsa_circ_291701,RMVar_hsa_circ_280308,RMVar_hsa_circ_95080,RMVar_hsa_circ_104519,RMVar_hsa_circ_129900,RMVar_hsa_circ_129902,RMVar_hsa_circ_129903,RMVar_hsa_circ_129901,RMVar_hsa_circ_129907,RMVar_hsa_circ_275156,RMVar_hsa_circ_316684,RMVar_hsa_circ_129899,RMVar_hsa_circ_357753,RMVar_hsa_circ_129908,RMVar_hsa_circ_307361,RMVar_hsa_circ_343338,RMVar_hsa_circ_329417,RMVar_hsa_circ_129911,RMVar_hsa_circ_129912,RMVar_hsa_circ_129913,RMVar_hsa_circ_30511,RMVar_hsa_circ_76618,RMVar_hsa_circ_357655,RMVar_hsa_circ_129914 9250 RMVar_ID_9250 Human_SNP_ID_5581416 A-to-I Human chr1 - 20774884 20774884 20774884 CACCTCCCAGGTTCAAGCGATTCTCCTGCCTCAACCTGCCAAGTAGCTGGGACTACAGGCGTGCA CACCTCCCAGGTTCAAGCGATTCTCCTGCCTCGACCTGCCAAGTAGCTGGGACTACAGGCGTGCA T C HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE100210;GSE99789;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,29796672,32596459 RNA-Seq:(High) rs1333969247 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41282,RMVar_hsa_circ_129876,RMVar_hsa_circ_129880,RMVar_hsa_circ_265631,RMVar_hsa_circ_267873,RMVar_hsa_circ_129881,RMVar_hsa_circ_129879,RMVar_hsa_circ_335005,RMVar_hsa_circ_291851,RMVar_hsa_circ_129884,RMVar_hsa_circ_337821,RMVar_hsa_circ_129889,RMVar_hsa_circ_89876,RMVar_hsa_circ_129898,RMVar_hsa_circ_277441,RMVar_hsa_circ_278114,RMVar_hsa_circ_273252,RMVar_hsa_circ_129896,RMVar_hsa_circ_129897,RMVar_hsa_circ_129895,RMVar_hsa_circ_288326,RMVar_hsa_circ_291701,RMVar_hsa_circ_280308,RMVar_hsa_circ_95080,RMVar_hsa_circ_104519,RMVar_hsa_circ_129900,RMVar_hsa_circ_129902,RMVar_hsa_circ_129903,RMVar_hsa_circ_129901,RMVar_hsa_circ_129907,RMVar_hsa_circ_275156,RMVar_hsa_circ_316684,RMVar_hsa_circ_129899,RMVar_hsa_circ_357753,RMVar_hsa_circ_129908,RMVar_hsa_circ_307361,RMVar_hsa_circ_343338,RMVar_hsa_circ_329417,RMVar_hsa_circ_129911,RMVar_hsa_circ_129912,RMVar_hsa_circ_129913,RMVar_hsa_circ_30511,RMVar_hsa_circ_76618,RMVar_hsa_circ_357655,RMVar_hsa_circ_129914 9251 RMVar_ID_9251 Human_SNP_ID_5581564 A-to-I Human chr1 - 20775406 20775406 20775406 TGGTGCACAGCTGTAGCCCTAGCTACTTAGGAAGCTGAGGTGGGGGGATTGCTTGAGTCCTGAAA TGGTGCACAGCTGTAGCCCTAGCTACTTAGGAGGCTGAGGTGGGGGGATTGCTTGAGTCCTGAAA T C HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE100210;GSE99789;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,29796672,31158229,32596459,32596459 RNA-Seq:(High) rs1165510369 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2119343,Human_RBP_ID_8296836,Human_RBP_ID_10749604,Human_RBP_ID_23360079 RMVar_hsa_circ_41282,RMVar_hsa_circ_129876,RMVar_hsa_circ_129880,RMVar_hsa_circ_265631,RMVar_hsa_circ_267873,RMVar_hsa_circ_129881,RMVar_hsa_circ_129879,RMVar_hsa_circ_335005,RMVar_hsa_circ_291851,RMVar_hsa_circ_129884,RMVar_hsa_circ_337821,RMVar_hsa_circ_129889,RMVar_hsa_circ_89876,RMVar_hsa_circ_129898,RMVar_hsa_circ_277441,RMVar_hsa_circ_278114,RMVar_hsa_circ_273252,RMVar_hsa_circ_129896,RMVar_hsa_circ_129897,RMVar_hsa_circ_129895,RMVar_hsa_circ_288326,RMVar_hsa_circ_291701,RMVar_hsa_circ_280308,RMVar_hsa_circ_95080,RMVar_hsa_circ_129900,RMVar_hsa_circ_129902,RMVar_hsa_circ_129903,RMVar_hsa_circ_129901,RMVar_hsa_circ_129907,RMVar_hsa_circ_275156,RMVar_hsa_circ_316684,RMVar_hsa_circ_129899,RMVar_hsa_circ_357753,RMVar_hsa_circ_129908,RMVar_hsa_circ_307361,RMVar_hsa_circ_343338,RMVar_hsa_circ_329417,RMVar_hsa_circ_129912,RMVar_hsa_circ_129913,RMVar_hsa_circ_30511,RMVar_hsa_circ_76618,RMVar_hsa_circ_357655,RMVar_hsa_circ_129914 9252 RMVar_ID_9252 Human_SNP_ID_5581574 A-to-I Human chr1 - 20775439 20775439 20775439 TTTACCAAAAACAAAGACACAAGCCGGACGCAATGGTGCACAGCTGTAGCCCTAGCTACTTAGGA TTTACCAAAAACAAAGACACAAGCCGGACGCATTGGTGCACAGCTGTAGCCCTAGCTACTTAGGA T A HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs191160834 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2119344,Human_RBP_ID_5747422,Human_RBP_ID_10749607,Human_RBP_ID_23360079,Human_RBP_ID_24449877 RMVar_hsa_circ_41282,RMVar_hsa_circ_129876,RMVar_hsa_circ_129880,RMVar_hsa_circ_265631,RMVar_hsa_circ_267873,RMVar_hsa_circ_129881,RMVar_hsa_circ_129879,RMVar_hsa_circ_335005,RMVar_hsa_circ_291851,RMVar_hsa_circ_129884,RMVar_hsa_circ_337821,RMVar_hsa_circ_129889,RMVar_hsa_circ_89876,RMVar_hsa_circ_129898,RMVar_hsa_circ_277441,RMVar_hsa_circ_278114,RMVar_hsa_circ_273252,RMVar_hsa_circ_129896,RMVar_hsa_circ_129897,RMVar_hsa_circ_129895,RMVar_hsa_circ_288326,RMVar_hsa_circ_291701,RMVar_hsa_circ_280308,RMVar_hsa_circ_95080,RMVar_hsa_circ_129900,RMVar_hsa_circ_129902,RMVar_hsa_circ_129903,RMVar_hsa_circ_129901,RMVar_hsa_circ_129907,RMVar_hsa_circ_275156,RMVar_hsa_circ_316684,RMVar_hsa_circ_129899,RMVar_hsa_circ_357753,RMVar_hsa_circ_129908,RMVar_hsa_circ_307361,RMVar_hsa_circ_343338,RMVar_hsa_circ_329417,RMVar_hsa_circ_129912,RMVar_hsa_circ_129913,RMVar_hsa_circ_30511,RMVar_hsa_circ_76618,RMVar_hsa_circ_357655,RMVar_hsa_circ_129914 9253 RMVar_ID_9253 Human_SNP_ID_5581575 A-to-I Human chr1 - 20775439 20775439 20775439 TTTACCAAAAACAAAGACACAAGCCGGACGCAATGGTGCACAGCTGTAGCCCTAGCTACTTAGGA TTTACCAAAAACAAAGACACAAGCCGGACGCAGTGGTGCACAGCTGTAGCCCTAGCTACTTAGGA T C HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs191160834 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2119344,Human_RBP_ID_5747422,Human_RBP_ID_10749607,Human_RBP_ID_23360079,Human_RBP_ID_24449877 RMVar_hsa_circ_41282,RMVar_hsa_circ_129876,RMVar_hsa_circ_129880,RMVar_hsa_circ_265631,RMVar_hsa_circ_267873,RMVar_hsa_circ_129881,RMVar_hsa_circ_129879,RMVar_hsa_circ_335005,RMVar_hsa_circ_291851,RMVar_hsa_circ_129884,RMVar_hsa_circ_337821,RMVar_hsa_circ_129889,RMVar_hsa_circ_89876,RMVar_hsa_circ_129898,RMVar_hsa_circ_277441,RMVar_hsa_circ_278114,RMVar_hsa_circ_273252,RMVar_hsa_circ_129896,RMVar_hsa_circ_129897,RMVar_hsa_circ_129895,RMVar_hsa_circ_288326,RMVar_hsa_circ_291701,RMVar_hsa_circ_280308,RMVar_hsa_circ_95080,RMVar_hsa_circ_129900,RMVar_hsa_circ_129902,RMVar_hsa_circ_129903,RMVar_hsa_circ_129901,RMVar_hsa_circ_129907,RMVar_hsa_circ_275156,RMVar_hsa_circ_316684,RMVar_hsa_circ_129899,RMVar_hsa_circ_357753,RMVar_hsa_circ_129908,RMVar_hsa_circ_307361,RMVar_hsa_circ_343338,RMVar_hsa_circ_329417,RMVar_hsa_circ_129912,RMVar_hsa_circ_129913,RMVar_hsa_circ_30511,RMVar_hsa_circ_76618,RMVar_hsa_circ_357655,RMVar_hsa_circ_129914 9254 RMVar_ID_9254 Human_SNP_ID_5583576 A-to-I Human chr1 - 20782532 20782532 20782532 TCACCTAGGCTGGAATGCAGTGGCTCGATTTCAGGTTACTGCATCCAAAACCTTCTGGGCTCAAG TCACCTAGGCTGGAATGCAGTGGCTCGATTTCGGGTTACTGCATCCAAAACCTTCTGGGCTCAAG T C HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs901938083 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10749865 RMVar_hsa_circ_95080,RMVar_hsa_circ_129899 9255 RMVar_ID_9255 Human_SNP_ID_5583773 A-to-I Human chr1 - 20783012 20783012 20783012 GAACTCCTGGACACTGGCAGTCCTCCCATCTCAGTCTTCCAAGTAGCTGGGACTACGGGCATGTG GAACTCCTGGACACTGGCAGTCCTCCCATCTCTGTCTTCCAAGTAGCTGGGACTACGGGCATGTG T A HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1413105876 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5747553,Human_RBP_ID_10749877 RMVar_hsa_circ_95080,RMVar_hsa_circ_129899 9256 RMVar_ID_9256 Human_SNP_ID_5583997 A-to-I Human chr1 - 20783726 20783726 20783726 TCACACTGTTACCCAGGCTGGAGTGCAGTGGCATGATCTCGGCTCACTGCAACTTCGGATTCCCG TCACACTGTTACCCAGGCTGGAGTGCAGTGGCGTGATCTCGGCTCACTGCAACTTCGGATTCCCG T C HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924654488 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9557827,Human_RBP_ID_24628862 RMVar_hsa_circ_95080,RMVar_hsa_circ_129899 9257 RMVar_ID_9257 Human_SNP_ID_5584177 A-to-I Human chr1 - 20784197 20784197 20784197 GAGAGGCCGAGGCAGATGGATCGCTTGAGCCCAGGAGTTTGTGACCAGCCTGGGCAACATGGCAA GAGAGGCCGAGGCAGATGGATCGCTTGAGCCCGGGAGTTTGTGACCAGCCTGGGCAACATGGCAA T C HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1192519658 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10749940 RMVar_hsa_circ_95080,RMVar_hsa_circ_129899 9258 RMVar_ID_9258 Human_SNP_ID_5584178 A-to-I Human chr1 - 20784197 20784197 20784197 GAGAGGCCGAGGCAGATGGATCGCTTGAGCCCAGGAGTTTGTGACCAGCCTGGGCAACATGGCAA GAGAGGCCGAGGCAGATGGATCGCTTGAGCCCCGGAGTTTGTGACCAGCCTGGGCAACATGGCAA T G HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1192519658 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10749940 RMVar_hsa_circ_95080,RMVar_hsa_circ_129899 9259 RMVar_ID_9259 Human_SNP_ID_5584192 A-to-I Human chr1 - 20784249 20784249 20784249 ATAGGTACACTGGGTCAGATGCAGTGGCTTACACCTGTAATCCCAACACGTTGAGAGGCCGAGGC ATAGGTACACTGGGTCAGATGCAGTGGCTTACGCCTGTAATCCCAACACGTTGAGAGGCCGAGGC T C HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs781048220 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5747584 RMVar_hsa_circ_95080,RMVar_hsa_circ_129899 9260 RMVar_ID_9260 Human_SNP_ID_5584466 A-to-I Human chr1 - 20784999 20784999 20784999 AGGAGATCGCTTGAGCCCAGGAGGTCGAGGCTACAGTGATCCCTGGTCATGCCACTGTACTCCAG AGGAGATCGCTTGAGCCCAGGAGGTCGAGGCTGCAGTGATCCCTGGTCATGCCACTGTACTCCAG T C HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs750959418 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1252523,Human_RBP_ID_10749968 RMVar_hsa_circ_95080,RMVar_hsa_circ_129899 9261 RMVar_ID_9261 Human_SNP_ID_5584472 A-to-I Human chr1 - 20785013 20785013 20785013 GTGGCTGAGGTGGGAGGAGATCGCTTGAGCCCAGGAGGTCGAGGCTACAGTGATCCCTGGTCATG GTGGCTGAGGTGGGAGGAGATCGCTTGAGCCCGGGAGGTCGAGGCTACAGTGATCCCTGGTCATG T C HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053269046 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95080,RMVar_hsa_circ_129899 9262 RMVar_ID_9262 Human_SNP_ID_5584473 A-to-I Human chr1 - 20785013 20785013 20785013 GTGGCTGAGGTGGGAGGAGATCGCTTGAGCCCAGGAGGTCGAGGCTACAGTGATCCCTGGTCATG GTGGCTGAGGTGGGAGGAGATCGCTTGAGCCCCGGAGGTCGAGGCTACAGTGATCCCTGGTCATG T G HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053269046 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95080,RMVar_hsa_circ_129899 9263 RMVar_ID_9263 Human_SNP_ID_5584505 A-to-I Human chr1 - 20785133 20785133 20785133 CCAAAGAGGAGGATCGCTTGAATCCAGGAGTTAGAGACCAGCTTGGGCAACCCTGTCTCTACAGA CCAAAGAGGAGGATCGCTTGAATCCAGGAGTTGGAGACCAGCTTGGGCAACCCTGTCTCTACAGA T C HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1179613607 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5747588,Human_RBP_ID_10749974,Human_RBP_ID_23360162 RMVar_hsa_circ_95080,RMVar_hsa_circ_129899 9264 RMVar_ID_9264 Human_SNP_ID_5591650 A-to-I Human chr1 - 20812232 20812232 20812232 TTCTTGAGATGGTGGGGGTCACTGTGTTGCCCAGGCTGGACCTGAACTCCTGGGCTTAAGCGGAT TTCTTGAGATGGTGGGGGTCACTGTGTTGCCCGGGCTGGACCTGAACTCCTGGGCTTAAGCGGAT T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1183429878 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_129920,RMVar_hsa_circ_129919,RMVar_hsa_circ_129922,RMVar_hsa_circ_276365 9265 RMVar_ID_9265 Human_SNP_ID_5606208 A-to-I Human chr1 - 20869456 20869456 20869456 ACTTCACATTTAAGAGCAAACTGTCCTTGGCCAGGAGTAGTGACACATGCCTATAATCCCAGCTA ACTTCACATTTAAGAGCAAACTGTCCTTGGCCGGGAGTAGTGACACATGCCTATAATCCCAGCTA T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1211855067 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4645,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_36834,RMVar_hsa_circ_120181,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_129930,RMVar_hsa_circ_129928,RMVar_hsa_circ_5635,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_129938,RMVar_hsa_circ_358241,RMVar_hsa_circ_58017,RMVar_hsa_circ_129941,RMVar_hsa_circ_368576,RMVar_hsa_circ_54961,RMVar_hsa_circ_35894,RMVar_hsa_circ_39504,RMVar_hsa_circ_129944,RMVar_hsa_circ_354001,RMVar_hsa_circ_110475,RMVar_hsa_circ_300918,RMVar_hsa_circ_65525,RMVar_hsa_circ_20412,RMVar_hsa_circ_356832,RMVar_hsa_circ_129949,RMVar_hsa_circ_129950,RMVar_hsa_circ_366470,RMVar_hsa_circ_281892,RMVar_hsa_circ_321815,RMVar_hsa_circ_365423,RMVar_hsa_circ_129951,RMVar_hsa_circ_29102,RMVar_hsa_circ_129952,RMVar_hsa_circ_346361 9266 RMVar_ID_9266 Human_SNP_ID_5606815 A-to-I Human chr1 - 20871999 20871999 20871999 GTGTGTGCTATGTTATTTTGTACTGTTGGAAAAGAAATGAATTAGCTGGGCATGGTGGCGCATGC GTGTGTGCTATGTTATTTTGTACTGTTGGAAAGGAAATGAATTAGCTGGGCATGGTGGCGCATGC T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs527674127 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4645,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_36834,RMVar_hsa_circ_120181,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_129930,RMVar_hsa_circ_129928,RMVar_hsa_circ_5635,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_129938,RMVar_hsa_circ_358241,RMVar_hsa_circ_58017,RMVar_hsa_circ_129941,RMVar_hsa_circ_368576,RMVar_hsa_circ_54961,RMVar_hsa_circ_35894,RMVar_hsa_circ_39504,RMVar_hsa_circ_129944,RMVar_hsa_circ_354001,RMVar_hsa_circ_110475,RMVar_hsa_circ_300918,RMVar_hsa_circ_65525,RMVar_hsa_circ_20412,RMVar_hsa_circ_356832,RMVar_hsa_circ_129949,RMVar_hsa_circ_129950,RMVar_hsa_circ_366470,RMVar_hsa_circ_281892,RMVar_hsa_circ_321815,RMVar_hsa_circ_365423,RMVar_hsa_circ_129951,RMVar_hsa_circ_29102,RMVar_hsa_circ_129952,RMVar_hsa_circ_346361 9267 RMVar_ID_9267 Human_SNP_ID_5606860 A-to-I Human chr1 - 20872191 20872191 20872191 TTGAGCCCAGGAGTTCAAGGATGCAGTGAGCTATGATGGCACTGTTGCATTCTAGCCTGGGTGAC TTGAGCCCAGGAGTTCAAGGATGCAGTGAGCTGTGATGGCACTGTTGCATTCTAGCCTGGGTGAC T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs535905763 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24629846 RMVar_hsa_circ_4645,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_36834,RMVar_hsa_circ_120181,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_129930,RMVar_hsa_circ_129928,RMVar_hsa_circ_5635,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_129938,RMVar_hsa_circ_358241,RMVar_hsa_circ_58017,RMVar_hsa_circ_129941,RMVar_hsa_circ_368576,RMVar_hsa_circ_54961,RMVar_hsa_circ_35894,RMVar_hsa_circ_39504,RMVar_hsa_circ_129944,RMVar_hsa_circ_354001,RMVar_hsa_circ_110475,RMVar_hsa_circ_300918,RMVar_hsa_circ_65525,RMVar_hsa_circ_20412,RMVar_hsa_circ_356832,RMVar_hsa_circ_129949,RMVar_hsa_circ_129950,RMVar_hsa_circ_366470,RMVar_hsa_circ_281892,RMVar_hsa_circ_321815,RMVar_hsa_circ_365423,RMVar_hsa_circ_129951,RMVar_hsa_circ_29102,RMVar_hsa_circ_129952,RMVar_hsa_circ_346361 9268 RMVar_ID_9268 Human_SNP_ID_5607543 A-to-I Human chr1 - 20875107 20875107 20875107 GGCATGATAGTAGTCCACCTGTAGTCCCAGCTACTAGGGAGGCTCAGGTGGGAGGATCCCTTGAG GGCATGATAGTAGTCCACCTGTAGTCCCAGCTTCTAGGGAGGCTCAGGTGGGAGGATCCCTTGAG T A EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991919519 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4645,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_36834,RMVar_hsa_circ_120181,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_129930,RMVar_hsa_circ_129928,RMVar_hsa_circ_5635,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_129938,RMVar_hsa_circ_358241,RMVar_hsa_circ_58017,RMVar_hsa_circ_129941,RMVar_hsa_circ_368576,RMVar_hsa_circ_54961,RMVar_hsa_circ_35894,RMVar_hsa_circ_39504,RMVar_hsa_circ_129944,RMVar_hsa_circ_354001,RMVar_hsa_circ_110475,RMVar_hsa_circ_300918,RMVar_hsa_circ_65525,RMVar_hsa_circ_20412,RMVar_hsa_circ_356832,RMVar_hsa_circ_129949,RMVar_hsa_circ_129950,RMVar_hsa_circ_366470,RMVar_hsa_circ_281892,RMVar_hsa_circ_321815,RMVar_hsa_circ_365423,RMVar_hsa_circ_129951,RMVar_hsa_circ_29102,RMVar_hsa_circ_129952,RMVar_hsa_circ_346361 9269 RMVar_ID_9269 Human_SNP_ID_5607661 A-to-I Human chr1 - 20875748 20875748 20875748 ACCACCATGTCCAGTTAATCTTTAAATTTTTTATAGAGACAGAATCTCAATATGTTGCCCAGACT ACCACCATGTCCAGTTAATCTTTAAATTTTTTGTAGAGACAGAATCTCAATATGTTGCCCAGACT T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1357923201 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4645,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_36834,RMVar_hsa_circ_120181,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_129930,RMVar_hsa_circ_129928,RMVar_hsa_circ_5635,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_129938,RMVar_hsa_circ_358241,RMVar_hsa_circ_58017,RMVar_hsa_circ_129941,RMVar_hsa_circ_368576,RMVar_hsa_circ_54961,RMVar_hsa_circ_35894,RMVar_hsa_circ_39504,RMVar_hsa_circ_129944,RMVar_hsa_circ_354001,RMVar_hsa_circ_110475,RMVar_hsa_circ_300918,RMVar_hsa_circ_65525,RMVar_hsa_circ_20412,RMVar_hsa_circ_356832,RMVar_hsa_circ_129949,RMVar_hsa_circ_129950,RMVar_hsa_circ_366470,RMVar_hsa_circ_281892,RMVar_hsa_circ_321815,RMVar_hsa_circ_365423,RMVar_hsa_circ_129951,RMVar_hsa_circ_29102,RMVar_hsa_circ_129952,RMVar_hsa_circ_346361 9270 RMVar_ID_9270 Human_SNP_ID_5607995 A-to-I Human chr1 - 20876975 20876975 20876975 GATTGTTTTATTTATGTATTTTGCTTGAGACAAGGTCTTTTGCTCTGTTGCCCAGGCTGGAGTCC GATTGTTTTATTTATGTATTTTGCTTGAGACAGGGTCTTTTGCTCTGTTGCCCAGGCTGGAGTCC T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1379023736 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4645,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_36834,RMVar_hsa_circ_120181,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_129930,RMVar_hsa_circ_129928,RMVar_hsa_circ_5635,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_129938,RMVar_hsa_circ_358241,RMVar_hsa_circ_58017,RMVar_hsa_circ_129941,RMVar_hsa_circ_368576,RMVar_hsa_circ_54961,RMVar_hsa_circ_35894,RMVar_hsa_circ_39504,RMVar_hsa_circ_129944,RMVar_hsa_circ_354001,RMVar_hsa_circ_110475,RMVar_hsa_circ_300918,RMVar_hsa_circ_65525,RMVar_hsa_circ_20412,RMVar_hsa_circ_356832,RMVar_hsa_circ_129949,RMVar_hsa_circ_129950,RMVar_hsa_circ_366470,RMVar_hsa_circ_281892,RMVar_hsa_circ_321815,RMVar_hsa_circ_365423,RMVar_hsa_circ_129951,RMVar_hsa_circ_29102,RMVar_hsa_circ_129952,RMVar_hsa_circ_346361 9271 RMVar_ID_9271 Human_SNP_ID_5617583 A-to-I Human chr1 - 20917493 20917493 20917493 TTTTGTCTGGCTTCTTTCTGAGATAGGGTCTCACTCTGTTACCTAGGTTGGAATGCAGTGGCACG TTTTGTCTGGCTTCTTTCTGAGATAGGGTCTCCCTCTGTTACCTAGGTTGGAATGCAGTGGCACG T G EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1044083963 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125099,RMVar_hsa_circ_115806,RMVar_hsa_circ_129929,RMVar_hsa_circ_129928,RMVar_hsa_circ_41188,RMVar_hsa_circ_58017,RMVar_hsa_circ_54961,RMVar_hsa_circ_35894,RMVar_hsa_circ_110475,RMVar_hsa_circ_129950,RMVar_hsa_circ_29102,RMVar_hsa_circ_39795,RMVar_hsa_circ_129956,RMVar_hsa_circ_69401,RMVar_hsa_circ_303446,RMVar_hsa_circ_267573,RMVar_hsa_circ_111740,RMVar_hsa_circ_16362,RMVar_hsa_circ_66039,RMVar_hsa_circ_129957,RMVar_hsa_circ_292177,RMVar_hsa_circ_366952,RMVar_hsa_circ_367934,RMVar_hsa_circ_340918,RMVar_hsa_circ_361048,RMVar_hsa_circ_302063,RMVar_hsa_circ_106190,RMVar_hsa_circ_270139,RMVar_hsa_circ_129968,RMVar_hsa_circ_129970,RMVar_hsa_circ_96722,RMVar_hsa_circ_129971,RMVar_hsa_circ_129969,RMVar_hsa_circ_129967,RMVar_hsa_circ_363666,RMVar_hsa_circ_2851,RMVar_hsa_circ_23984,RMVar_hsa_circ_284998,RMVar_hsa_circ_129973 9272 RMVar_ID_9272 Human_SNP_ID_5622934 A-to-I Human chr1 - 20940030 20940030 20940030 GCAACACAGTGAAACCCCATCTCCACTGACATACAAAAAAAATAGCCAGGCATGGCAGTGTGGGC GCAACACAGTGAAACCCCATCTCCACTGACATCCAAAAAAAATAGCCAGGCATGGCAGTGTGGGC T G EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs561451201 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125099,RMVar_hsa_circ_115806,RMVar_hsa_circ_129929,RMVar_hsa_circ_129928,RMVar_hsa_circ_41188,RMVar_hsa_circ_58017,RMVar_hsa_circ_54961,RMVar_hsa_circ_35894,RMVar_hsa_circ_110475,RMVar_hsa_circ_129950,RMVar_hsa_circ_29102,RMVar_hsa_circ_39795,RMVar_hsa_circ_129956,RMVar_hsa_circ_69401,RMVar_hsa_circ_303446,RMVar_hsa_circ_267573,RMVar_hsa_circ_111740,RMVar_hsa_circ_16362,RMVar_hsa_circ_66039,RMVar_hsa_circ_129957,RMVar_hsa_circ_292177,RMVar_hsa_circ_366952,RMVar_hsa_circ_367934,RMVar_hsa_circ_340918,RMVar_hsa_circ_361048,RMVar_hsa_circ_302063,RMVar_hsa_circ_106190,RMVar_hsa_circ_270139,RMVar_hsa_circ_129968,RMVar_hsa_circ_129970,RMVar_hsa_circ_96722,RMVar_hsa_circ_129971,RMVar_hsa_circ_129969,RMVar_hsa_circ_129967,RMVar_hsa_circ_363666,RMVar_hsa_circ_2851,RMVar_hsa_circ_23984,RMVar_hsa_circ_284998,RMVar_hsa_circ_129973 9273 RMVar_ID_9273 Human_SNP_ID_5624468 A-to-I Human chr1 - 20945665 20945665 20945665 AGCTCAAGAATTCAAGACCAGCTGAGTAACATAGCGATACCCTGTCTCTACAAAAAATAAAAATA AGCTCAAGAATTCAAGACCAGCTGAGTAACATGGCGATACCCTGTCTCTACAAAAAATAAAAATA T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1359331121 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125099,RMVar_hsa_circ_115806,RMVar_hsa_circ_129929,RMVar_hsa_circ_129928,RMVar_hsa_circ_41188,RMVar_hsa_circ_54961,RMVar_hsa_circ_35894,RMVar_hsa_circ_110475,RMVar_hsa_circ_129950,RMVar_hsa_circ_39795,RMVar_hsa_circ_129956,RMVar_hsa_circ_69401,RMVar_hsa_circ_267573,RMVar_hsa_circ_111740,RMVar_hsa_circ_16362,RMVar_hsa_circ_66039,RMVar_hsa_circ_367934,RMVar_hsa_circ_340918,RMVar_hsa_circ_361048,RMVar_hsa_circ_302063,RMVar_hsa_circ_106190,RMVar_hsa_circ_270139,RMVar_hsa_circ_129968,RMVar_hsa_circ_129970,RMVar_hsa_circ_96722,RMVar_hsa_circ_129971,RMVar_hsa_circ_129969,RMVar_hsa_circ_363666,RMVar_hsa_circ_129977,RMVar_hsa_circ_84891,RMVar_hsa_circ_2851,RMVar_hsa_circ_325784,RMVar_hsa_circ_341512,RMVar_hsa_circ_129975,RMVar_hsa_circ_378276,RMVar_hsa_circ_333173,RMVar_hsa_circ_292561,RMVar_hsa_circ_23431,RMVar_hsa_circ_276834,RMVar_hsa_circ_129978,RMVar_hsa_circ_129979 9274 RMVar_ID_9274 Human_SNP_ID_5624818 A-to-I Human chr1 - 20947338 20947338 20947338 ATTTTTTTTTCTTTTTTCTTCTATTTTGAGACAGGGTTTCGTTCTATCACCCAGGATGGAGTGCA ATTTTTTTTTCTTTTTTCTTCTATTTTGAGACGGGGTTTCGTTCTATCACCCAGGATGGAGTGCA T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1417514060 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5750748 RMVar_hsa_circ_125099,RMVar_hsa_circ_115806,RMVar_hsa_circ_129929,RMVar_hsa_circ_129928,RMVar_hsa_circ_41188,RMVar_hsa_circ_54961,RMVar_hsa_circ_35894,RMVar_hsa_circ_110475,RMVar_hsa_circ_129950,RMVar_hsa_circ_39795,RMVar_hsa_circ_129956,RMVar_hsa_circ_69401,RMVar_hsa_circ_267573,RMVar_hsa_circ_111740,RMVar_hsa_circ_16362,RMVar_hsa_circ_66039,RMVar_hsa_circ_367934,RMVar_hsa_circ_340918,RMVar_hsa_circ_361048,RMVar_hsa_circ_302063,RMVar_hsa_circ_106190,RMVar_hsa_circ_270139,RMVar_hsa_circ_129968,RMVar_hsa_circ_129970,RMVar_hsa_circ_96722,RMVar_hsa_circ_129971,RMVar_hsa_circ_129969,RMVar_hsa_circ_363666,RMVar_hsa_circ_129977,RMVar_hsa_circ_84891,RMVar_hsa_circ_2851,RMVar_hsa_circ_325784,RMVar_hsa_circ_341512,RMVar_hsa_circ_129975,RMVar_hsa_circ_378276,RMVar_hsa_circ_333173,RMVar_hsa_circ_292561,RMVar_hsa_circ_23431,RMVar_hsa_circ_276834,RMVar_hsa_circ_129978,RMVar_hsa_circ_129979 9275 RMVar_ID_9275 Human_SNP_ID_5626052 A-to-I Human chr1 - 20952338 20952338 20952338 CACCCTGGCTAACATGGTGAAACCCTGTCTCTACTAAAATACAAAAAATTAGTTTGGGTGTGGTG CACCCTGGCTAACATGGTGAAACCCTGTCTCTGCTAAAATACAAAAAATTAGTTTGGGTGTGGTG T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1465728755 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17737845 RMVar_hsa_circ_125099,RMVar_hsa_circ_115806,RMVar_hsa_circ_129929,RMVar_hsa_circ_129928,RMVar_hsa_circ_41188,RMVar_hsa_circ_54961,RMVar_hsa_circ_35894,RMVar_hsa_circ_110475,RMVar_hsa_circ_129950,RMVar_hsa_circ_39795,RMVar_hsa_circ_129956,RMVar_hsa_circ_69401,RMVar_hsa_circ_267573,RMVar_hsa_circ_111740,RMVar_hsa_circ_66039,RMVar_hsa_circ_367934,RMVar_hsa_circ_340918,RMVar_hsa_circ_361048,RMVar_hsa_circ_302063,RMVar_hsa_circ_106190,RMVar_hsa_circ_270139,RMVar_hsa_circ_129968,RMVar_hsa_circ_129970,RMVar_hsa_circ_96722,RMVar_hsa_circ_129971,RMVar_hsa_circ_129969,RMVar_hsa_circ_363666,RMVar_hsa_circ_84891,RMVar_hsa_circ_2851,RMVar_hsa_circ_325784,RMVar_hsa_circ_341512,RMVar_hsa_circ_129975,RMVar_hsa_circ_378276,RMVar_hsa_circ_23431,RMVar_hsa_circ_276834,RMVar_hsa_circ_129978,RMVar_hsa_circ_129979,RMVar_hsa_circ_129982,RMVar_hsa_circ_305003,RMVar_hsa_circ_327897,RMVar_hsa_circ_365884,RMVar_hsa_circ_335751,RMVar_hsa_circ_317867,RMVar_hsa_circ_274297,RMVar_hsa_circ_28615,RMVar_hsa_circ_129983,RMVar_hsa_circ_129980,RMVar_hsa_circ_129981 9276 RMVar_ID_9276 Human_SNP_ID_5626801 A-to-I Human chr1 - 20955323 20955322 20955324 GGAGGCTGAGGTGGAAGGAACACTTGAACTCAAGAGGTCGAGGCTGCAGTGAGCTGTGATTGCAC GGAGGCTGAGGTGGAAGGAACACTTGAACTC__GAGGTCGAGGCTGCAGTGAGCTGTGATTGCAC CTT C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1169520605 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_125099,RMVar_hsa_circ_115806,RMVar_hsa_circ_129929,RMVar_hsa_circ_129928,RMVar_hsa_circ_41188,RMVar_hsa_circ_54961,RMVar_hsa_circ_35894,RMVar_hsa_circ_110475,RMVar_hsa_circ_129950,RMVar_hsa_circ_39795,RMVar_hsa_circ_129956,RMVar_hsa_circ_69401,RMVar_hsa_circ_267573,RMVar_hsa_circ_111740,RMVar_hsa_circ_66039,RMVar_hsa_circ_367934,RMVar_hsa_circ_340918,RMVar_hsa_circ_361048,RMVar_hsa_circ_302063,RMVar_hsa_circ_106190,RMVar_hsa_circ_270139,RMVar_hsa_circ_129968,RMVar_hsa_circ_129970,RMVar_hsa_circ_96722,RMVar_hsa_circ_129971,RMVar_hsa_circ_129969,RMVar_hsa_circ_363666,RMVar_hsa_circ_84891,RMVar_hsa_circ_2851,RMVar_hsa_circ_325784,RMVar_hsa_circ_341512,RMVar_hsa_circ_129975,RMVar_hsa_circ_378276,RMVar_hsa_circ_23431,RMVar_hsa_circ_276834,RMVar_hsa_circ_129978,RMVar_hsa_circ_129979,RMVar_hsa_circ_129982,RMVar_hsa_circ_305003,RMVar_hsa_circ_327897,RMVar_hsa_circ_365884,RMVar_hsa_circ_335751,RMVar_hsa_circ_317867,RMVar_hsa_circ_274297,RMVar_hsa_circ_28615,RMVar_hsa_circ_129983,RMVar_hsa_circ_129980,RMVar_hsa_circ_129981 9277 RMVar_ID_9277 Human_SNP_ID_5630818 A-to-I Human chr1 - 20971771 20971771 20971771 AAATTAGCTGGGTGTGGAGGCTCGTGCCTATAATTCCAGCTACTCGGGAGGCTGAGGCACGAGAA AAATTAGCTGGGTGTGGAGGCTCGTGCCTATAGTTCCAGCTACTCGGGAGGCTGAGGCACGAGAA T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs557000020 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125099,RMVar_hsa_circ_115806,RMVar_hsa_circ_129929,RMVar_hsa_circ_129928,RMVar_hsa_circ_41188,RMVar_hsa_circ_54961,RMVar_hsa_circ_35894,RMVar_hsa_circ_110475,RMVar_hsa_circ_129950,RMVar_hsa_circ_39795,RMVar_hsa_circ_129956,RMVar_hsa_circ_69401,RMVar_hsa_circ_267573,RMVar_hsa_circ_111740,RMVar_hsa_circ_66039,RMVar_hsa_circ_367934,RMVar_hsa_circ_340918,RMVar_hsa_circ_361048,RMVar_hsa_circ_302063,RMVar_hsa_circ_106190,RMVar_hsa_circ_270139,RMVar_hsa_circ_129968,RMVar_hsa_circ_129970,RMVar_hsa_circ_96722,RMVar_hsa_circ_129971,RMVar_hsa_circ_129969,RMVar_hsa_circ_363666,RMVar_hsa_circ_84891,RMVar_hsa_circ_2851,RMVar_hsa_circ_325784,RMVar_hsa_circ_341512,RMVar_hsa_circ_129975,RMVar_hsa_circ_378276,RMVar_hsa_circ_23431,RMVar_hsa_circ_276834,RMVar_hsa_circ_129978,RMVar_hsa_circ_129979,RMVar_hsa_circ_266691,RMVar_hsa_circ_129982,RMVar_hsa_circ_305003,RMVar_hsa_circ_327897,RMVar_hsa_circ_365884,RMVar_hsa_circ_335751,RMVar_hsa_circ_317867,RMVar_hsa_circ_274297,RMVar_hsa_circ_28615,RMVar_hsa_circ_129983,RMVar_hsa_circ_279482,RMVar_hsa_circ_129980,RMVar_hsa_circ_129981,RMVar_hsa_circ_316610,RMVar_hsa_circ_331706,RMVar_hsa_circ_333328,RMVar_hsa_circ_289888,RMVar_hsa_circ_277928,RMVar_hsa_circ_279173,RMVar_hsa_circ_269566,RMVar_hsa_circ_129986,RMVar_hsa_circ_129988,RMVar_hsa_circ_129987,RMVar_hsa_circ_129984,RMVar_hsa_circ_129985 9278 RMVar_ID_9278 Human_SNP_ID_5630819 A-to-I Human chr1 - 20971774 20971774 20971774 CAAAAATTAGCTGGGTGTGGAGGCTCGTGCCTATAATTCCAGCTACTCGGGAGGCTGAGGCACGA CAAAAATTAGCTGGGTGTGGAGGCTCGTGCCTGTAATTCCAGCTACTCGGGAGGCTGAGGCACGA T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1303963815 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125099,RMVar_hsa_circ_115806,RMVar_hsa_circ_129929,RMVar_hsa_circ_129928,RMVar_hsa_circ_41188,RMVar_hsa_circ_54961,RMVar_hsa_circ_35894,RMVar_hsa_circ_110475,RMVar_hsa_circ_129950,RMVar_hsa_circ_39795,RMVar_hsa_circ_129956,RMVar_hsa_circ_69401,RMVar_hsa_circ_267573,RMVar_hsa_circ_111740,RMVar_hsa_circ_66039,RMVar_hsa_circ_367934,RMVar_hsa_circ_340918,RMVar_hsa_circ_361048,RMVar_hsa_circ_302063,RMVar_hsa_circ_106190,RMVar_hsa_circ_270139,RMVar_hsa_circ_129968,RMVar_hsa_circ_129970,RMVar_hsa_circ_96722,RMVar_hsa_circ_129971,RMVar_hsa_circ_129969,RMVar_hsa_circ_363666,RMVar_hsa_circ_84891,RMVar_hsa_circ_2851,RMVar_hsa_circ_325784,RMVar_hsa_circ_341512,RMVar_hsa_circ_129975,RMVar_hsa_circ_378276,RMVar_hsa_circ_23431,RMVar_hsa_circ_276834,RMVar_hsa_circ_129978,RMVar_hsa_circ_129979,RMVar_hsa_circ_266691,RMVar_hsa_circ_129982,RMVar_hsa_circ_305003,RMVar_hsa_circ_327897,RMVar_hsa_circ_365884,RMVar_hsa_circ_335751,RMVar_hsa_circ_317867,RMVar_hsa_circ_274297,RMVar_hsa_circ_28615,RMVar_hsa_circ_129983,RMVar_hsa_circ_279482,RMVar_hsa_circ_129980,RMVar_hsa_circ_129981,RMVar_hsa_circ_316610,RMVar_hsa_circ_331706,RMVar_hsa_circ_333328,RMVar_hsa_circ_289888,RMVar_hsa_circ_277928,RMVar_hsa_circ_279173,RMVar_hsa_circ_269566,RMVar_hsa_circ_129986,RMVar_hsa_circ_129988,RMVar_hsa_circ_129987,RMVar_hsa_circ_129984,RMVar_hsa_circ_129985 9279 RMVar_ID_9279 Human_SNP_ID_5649036 A-to-I Human chr1 - 21045114 21045114 21045114 TGTTTTTTTATTTATTTTTTATTTTTAGAGACAGGACCTCACTCTGTCACCCAGGCTGGAGTGCA TGTTTTTTTATTTATTTTTTATTTTTAGAGACGGGACCTCACTCTGTCACCCAGGCTGGAGTGCA T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1327317848 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5752694,Human_RBP_ID_10764539 RMVar_hsa_circ_125099,RMVar_hsa_circ_115806,RMVar_hsa_circ_129929,RMVar_hsa_circ_129928,RMVar_hsa_circ_41188,RMVar_hsa_circ_54961,RMVar_hsa_circ_35894,RMVar_hsa_circ_129956,RMVar_hsa_circ_69401,RMVar_hsa_circ_111740,RMVar_hsa_circ_367934,RMVar_hsa_circ_361048,RMVar_hsa_circ_302063,RMVar_hsa_circ_270139,RMVar_hsa_circ_129970,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_327897,RMVar_hsa_circ_365884,RMVar_hsa_circ_317867,RMVar_hsa_circ_129983,RMVar_hsa_circ_333328,RMVar_hsa_circ_289888,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_284054,RMVar_hsa_circ_112494,RMVar_hsa_circ_93832,RMVar_hsa_circ_129995,RMVar_hsa_circ_129996,RMVar_hsa_circ_333347,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_130004,RMVar_hsa_circ_270666,RMVar_hsa_circ_130002,RMVar_hsa_circ_130003,RMVar_hsa_circ_272861,RMVar_hsa_circ_303313,RMVar_hsa_circ_130006,RMVar_hsa_circ_130007,RMVar_hsa_circ_130005 9280 RMVar_ID_9280 Human_SNP_ID_5649038 A-to-I Human chr1 - 21045116 21045116 21045116 GCTGTTTTTTTATTTATTTTTTATTTTTAGAGACAGGACCTCACTCTGTCACCCAGGCTGGAGTG GCTGTTTTTTTATTTATTTTTTATTTTTAGAGGCAGGACCTCACTCTGTCACCCAGGCTGGAGTG T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991119014 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5752694,Human_RBP_ID_10764539 RMVar_hsa_circ_125099,RMVar_hsa_circ_115806,RMVar_hsa_circ_129929,RMVar_hsa_circ_129928,RMVar_hsa_circ_41188,RMVar_hsa_circ_54961,RMVar_hsa_circ_35894,RMVar_hsa_circ_129956,RMVar_hsa_circ_69401,RMVar_hsa_circ_111740,RMVar_hsa_circ_367934,RMVar_hsa_circ_361048,RMVar_hsa_circ_302063,RMVar_hsa_circ_270139,RMVar_hsa_circ_129970,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_327897,RMVar_hsa_circ_365884,RMVar_hsa_circ_317867,RMVar_hsa_circ_129983,RMVar_hsa_circ_333328,RMVar_hsa_circ_289888,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_284054,RMVar_hsa_circ_112494,RMVar_hsa_circ_93832,RMVar_hsa_circ_129995,RMVar_hsa_circ_129996,RMVar_hsa_circ_333347,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_130004,RMVar_hsa_circ_270666,RMVar_hsa_circ_130002,RMVar_hsa_circ_130003,RMVar_hsa_circ_272861,RMVar_hsa_circ_303313,RMVar_hsa_circ_130006,RMVar_hsa_circ_130007,RMVar_hsa_circ_130005 9281 RMVar_ID_9281 Human_SNP_ID_5650554 A-to-I Human chr1 - 21051777 21051777 21051777 TCACTGTAAGCCTTGAACTCCTGGGCCCAAGCAGTCCTTTTGCCTCAGCTTCCCAAGTAACTATT TCACTGTAAGCCTTGAACTCCTGGGCCCAAGCCGTCCTTTTGCCTCAGCTTCCCAAGTAACTATT T G EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1011976994 Functional Loss SNV dbSNP153 33..33 33 - - - 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_97119,RMVar_hsa_circ_89249,RMVar_hsa_circ_130015,RMVar_hsa_circ_130017,RMVar_hsa_circ_83587,RMVar_hsa_circ_130016,RMVar_hsa_circ_130013,RMVar_hsa_circ_130014,RMVar_hsa_circ_130012,RMVar_hsa_circ_130010 9282 RMVar_ID_9282 Human_SNP_ID_5655598 A-to-I Human chr1 - 21071222 21071222 21071222 TGTTTCATTTTCTGTAGTGACAGGATCTCACTATGTTGCCCAGGCTGGTCTAGAACTCCTGGCCT TGTTTCATTTTCTGTAGTGACAGGATCTCACTGTGTTGCCCAGGCTGGTCTAGAACTCCTGGCCT T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900343607 Functional Loss SNV dbSNP153 33..33 33 - - - 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 9283 RMVar_ID_9283 Human_SNP_ID_5655599 A-to-I Human chr1 - 21071222 21071222 21071222 TGTTTCATTTTCTGTAGTGACAGGATCTCACTATGTTGCCCAGGCTGGTCTAGAACTCCTGGCCT TGTTTCATTTTCTGTAGTGACAGGATCTCACTCTGTTGCCCAGGCTGGTCTAGAACTCCTGGCCT T G EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900343607 Functional Loss SNV dbSNP153 33..33 33 - - - 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 9284 RMVar_ID_9284 Human_SNP_ID_5658191 A-to-I Human chr1 - 21082075 21082075 21082075 AAAGTCAGACTTGGCCAGGCACGGTGGCTCACACTTGTCATCCTGGTACTTTGGGAGGCCAAGGT AAAGTCAGACTTGGCCAGGCACGGTGGCTCACGCTTGTCATCCTGGTACTTTGGGAGGCCAAGGT T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388625223 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10764930 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 9285 RMVar_ID_9285 Human_SNP_ID_5659636 A-to-I Human chr1 - 21087766 21087766 21087766 AGCCGGACATGGTGGCGGGCGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATGGCG AGCCGGACATGGTGGCGGGCGCCTGTAGTCCCGGCTACTCAGGAGGCTGAGGCAGGAGAATGGCG T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs368909989 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_95813 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 9286 RMVar_ID_9286 Human_SNP_ID_5662316 A-to-I Human chr1 - 21098932 21098932 21098932 CATTCATTTAAAACTTTTCCCCATTTGAGGCTAGGCACAGTGGGTCGTGCCTATAATCCCAGCAC CATTCATTTAAAACTTTTCCCCATTTGAGGCTGGGCACAGTGGGTCGTGCCTATAATCCCAGCAC T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1321811267 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125099,RMVar_hsa_circ_115806,RMVar_hsa_circ_129929,RMVar_hsa_circ_129928,RMVar_hsa_circ_35894,RMVar_hsa_circ_69401,RMVar_hsa_circ_270139,RMVar_hsa_circ_363666,RMVar_hsa_circ_84891,RMVar_hsa_circ_341512,RMVar_hsa_circ_129975,RMVar_hsa_circ_129979,RMVar_hsa_circ_365884,RMVar_hsa_circ_129983,RMVar_hsa_circ_277928,RMVar_hsa_circ_129991,RMVar_hsa_circ_129984,RMVar_hsa_circ_104222,RMVar_hsa_circ_302688,RMVar_hsa_circ_93832,RMVar_hsa_circ_129996,RMVar_hsa_circ_129997,RMVar_hsa_circ_360070,RMVar_hsa_circ_129998,RMVar_hsa_circ_130011,RMVar_hsa_circ_85432,RMVar_hsa_circ_270666,RMVar_hsa_circ_130007,RMVar_hsa_circ_281334,RMVar_hsa_circ_93947,RMVar_hsa_circ_89249,RMVar_hsa_circ_83587,RMVar_hsa_circ_130013,RMVar_hsa_circ_130014,RMVar_hsa_circ_130012,RMVar_hsa_circ_130010,RMVar_hsa_circ_125788,RMVar_hsa_circ_278256,RMVar_hsa_circ_130023,RMVar_hsa_circ_130024,RMVar_hsa_circ_130022 9287 RMVar_ID_9287 Human_SNP_ID_5664437 A-to-I Human chr1 - 21108072 21108072 21108072 GTGTGATCTCAACACTGCATCCTCTGCCTCCCAGGCTTAAGCGATCCTTCCGCTTCAATCTCCTA GTGTGATCTCAACACTGCATCCTCTGCCTCCCGGGCTTAAGCGATCCTTCCGCTTCAATCTCCTA T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1018478109 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125099,RMVar_hsa_circ_115806,RMVar_hsa_circ_129929,RMVar_hsa_circ_129928,RMVar_hsa_circ_35894,RMVar_hsa_circ_69401,RMVar_hsa_circ_270139,RMVar_hsa_circ_363666,RMVar_hsa_circ_84891,RMVar_hsa_circ_341512,RMVar_hsa_circ_129975,RMVar_hsa_circ_129979,RMVar_hsa_circ_365884,RMVar_hsa_circ_129983,RMVar_hsa_circ_277928,RMVar_hsa_circ_129991,RMVar_hsa_circ_129984,RMVar_hsa_circ_104222,RMVar_hsa_circ_302688,RMVar_hsa_circ_93832,RMVar_hsa_circ_129996,RMVar_hsa_circ_129997,RMVar_hsa_circ_360070,RMVar_hsa_circ_129998,RMVar_hsa_circ_130011,RMVar_hsa_circ_85432,RMVar_hsa_circ_270666,RMVar_hsa_circ_130007,RMVar_hsa_circ_281334,RMVar_hsa_circ_93947,RMVar_hsa_circ_89249,RMVar_hsa_circ_83587,RMVar_hsa_circ_130013,RMVar_hsa_circ_130014,RMVar_hsa_circ_130012,RMVar_hsa_circ_102918,RMVar_hsa_circ_130010,RMVar_hsa_circ_125788,RMVar_hsa_circ_278256,RMVar_hsa_circ_130023,RMVar_hsa_circ_130024,RMVar_hsa_circ_130022,RMVar_hsa_circ_130025 9288 RMVar_ID_9288 Human_SNP_ID_5665845 A-to-I Human chr1 - 21113845 21113845 21113845 CATCCAGCTAATTTTTTGTATTTTTTGAAGAGACGGGGTTTTACCATGTTGCTCAGGATAGTCTC CATCCAGCTAATTTTTTGTATTTTTTGAAGAGGCGGGGTTTTACCATGTTGCTCAGGATAGTCTC T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1043126868 Functional Loss SNV dbSNP153 33..33 33 - - - 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 9289 RMVar_ID_9289 Human_SNP_ID_5666343 A-to-I Human chr1 - 21115828 21115828 21115828 TGTATATTCCTAGATACTTGGGAGACTGAGGCAGGAGGACCGTTTGAGCCCAGGAGTTCACGGGT TGTATATTCCTAGATACTTGGGAGACTGAGGCGGGAGGACCGTTTGAGCCCAGGAGTTCACGGGT T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264992436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5753246 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 9290 RMVar_ID_9290 Human_SNP_ID_5666376 A-to-I Human chr1 - 21115969 21115969 21115969 CTGTAATCGTAGCACTTTGGGAGGCTGAGGCAAGAGGATTGGTTAAGGCCAGGAGTTCTAGACCA CTGTAATCGTAGCACTTTGGGAGGCTGAGGCAGGAGGATTGGTTAAGGCCAGGAGTTCTAGACCA T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1020013129 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24633983 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 9291 RMVar_ID_9291 Human_SNP_ID_5666377 A-to-I Human chr1 - 21115997 21115990 21115997 TAAATTGTCTGGGCACAGTGGCTCACACCTGTAATCGTAGCACTTTGGGAGGCTGAGGCAAGAGG TAAATTGTCTGGGCACAGTGGCTCACACCTGT_______GCACTTTGGGAGGCTGAGGCAAGAGG CTACGATT C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1209011801 Functional Loss DEL dbSNP153 33..39 33 - - - 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 9292 RMVar_ID_9292 Human_SNP_ID_5667650 A-to-I Human chr1 - 21120982 21120982 21120982 CCAGGAAGTTGAGGCTGTAGAGAGTCAGGATCATGCCACTGCATTCCAGCCTGGGTGACAGAGTG CCAGGAAGTTGAGGCTGTAGAGAGTCAGGATCCTGCCACTGCATTCCAGCCTGGGTGACAGAGTG T G EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs576996733 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10765611,Human_RBP_ID_24634091 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 9293 RMVar_ID_9293 Human_SNP_ID_5669692 A-to-I Human chr1 - 21129264 21129264 21129264 GTTGCCCAGGCTGGAGTGCAGTGGTGCAATCTAGGCTTACCGCAACCTCTGCCTCCCAGGTTCAA GTTGCCCAGGCTGGAGTGCAGTGGTGCAATCTGGGCTTACCGCAACCTCTGCCTCCCAGGTTCAA T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs531396672 Functional Loss SNV dbSNP153 33..33 33 - - - 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 9294 RMVar_ID_9294 Human_SNP_ID_5669920 A-to-I Human chr1 - 21130167 21130167 21130167 GTTGCCCAGTCTGGTCTTCAACTCTTGGGCTCATGTGATCCTCCCGCCTTGTCCTCCCAAAGTGC GTTGCCCAGTCTGGTCTTCAACTCTTGGGCTCTTGTGATCCTCCCGCCTTGTCCTCCCAAAGTGC T A EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs989763201 Functional Loss SNV dbSNP153 33..33 33 - - - 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 9295 RMVar_ID_9295 Human_SNP_ID_5669921 A-to-I Human chr1 - 21130167 21130167 21130167 GTTGCCCAGTCTGGTCTTCAACTCTTGGGCTCATGTGATCCTCCCGCCTTGTCCTCCCAAAGTGC GTTGCCCAGTCTGGTCTTCAACTCTTGGGCTCGTGTGATCCTCCCGCCTTGTCCTCCCAAAGTGC T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs989763201 Functional Loss SNV dbSNP153 33..33 33 - - - 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 9296 RMVar_ID_9296 Human_SNP_ID_5669922 A-to-I Human chr1 - 21130167 21130167 21130167 GTTGCCCAGTCTGGTCTTCAACTCTTGGGCTCATGTGATCCTCCCGCCTTGTCCTCCCAAAGTGC GTTGCCCAGTCTGGTCTTCAACTCTTGGGCTCCTGTGATCCTCCCGCCTTGTCCTCCCAAAGTGC T G EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs989763201 Functional Loss SNV dbSNP153 33..33 33 - - - 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 9297 RMVar_ID_9297 Human_SNP_ID_5670372 A-to-I Human chr1 - 21131790 21131790 21131790 GTTTTCTGTTTCTTGTAGAGATGGGTTTTGCCATGTTGGCTAGGCTAGTCTCAAACTTCTCGGCT GTTTTCTGTTTCTTGTAGAGATGGGTTTTGCCGTGTTGGCTAGGCTAGTCTCAAACTTCTCGGCT T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs992167370 Functional Loss SNV dbSNP153 33..33 33 - - - 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 9298 RMVar_ID_9298 Human_SNP_ID_5670405 A-to-I Human chr1 - 21131964 21131964 21131964 TTTGATTATTAAAAAAATTTTTTTTTTGAGACAGTGTCTCACTGTTTCCCAGGCTGGAGTGCAGT TTTGATTATTAAAAAAATTTTTTTTTTGAGACGGTGTCTCACTGTTTCCCAGGCTGGAGTGCAGT T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs529324990 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10766510 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 9299 RMVar_ID_9299 Human_SNP_ID_5670562 A-to-I Human chr1 - 21132639 21132639 21132639 GCCCAGGAGTTTGACACCAGCCTACACAACATAGTGACACCCCATCTCTACAAAAAAATAAAAAA GCCCAGGAGTTTGACACCAGCCTACACAACATGGTGACACCCCATCTCTACAAAAAAATAAAAAA T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1184345135 Functional Loss SNV dbSNP153 33..33 33 - - - 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 9300 RMVar_ID_9300 Human_SNP_ID_5670738 A-to-I Human chr1 - 21133353 21133353 21133353 GGGCGTGGTGGCACACGCCTGTAGTCCCAGCTACTCCGGAGGCTGAGGCAGTAGAATTGCTGGAA GGGCGTGGTGGCACACGCCTGTAGTCCCAGCTGCTCCGGAGGCTGAGGCAGTAGAATTGCTGGAA T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1426536142 Functional Loss SNV dbSNP153 33..33 33 - - - 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 9301 RMVar_ID_9301 Human_SNP_ID_5670743 A-to-I Human chr1 - 21133363 21133363 21133363 AAAATTAGCCGGGCGTGGTGGCACACGCCTGTAGTCCCAGCTACTCCGGAGGCTGAGGCAGTAGA AAAATTAGCCGGGCGTGGTGGCACACGCCTGTGGTCCCAGCTACTCCGGAGGCTGAGGCAGTAGA T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1344688899 Functional Loss SNV dbSNP153 33..33 33 - - - 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 9302 RMVar_ID_9302 Human_SNP_ID_5671725 A-to-I Human chr1 - 21137353 21137353 21137353 ATCGCTTGAAGCCAGAGTTTGAGACCAGCCTGAGCAGTGTAGTGAGACCTCGTCTCTACAAAAAT ATCGCTTGAAGCCAGAGTTTGAGACCAGCCTGGGCAGTGTAGTGAGACCTCGTCTCTACAAAAAT T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1229334646 Functional Loss SNV dbSNP153 33..33 33 - - - 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 9303 RMVar_ID_9303 Human_SNP_ID_5671785 A-to-I Human chr1 - 21137642 21137642 21137642 TATTATTGTTATTATTATTTTTTAATTTTGTAAAGATAAGGTCTTACTATGTTGCCCAGGCTGGT TATTATTGTTATTATTATTTTTTAATTTTGTAGAGATAAGGTCTTACTATGTTGCCCAGGCTGGT T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1012374962 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10766842 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 9304 RMVar_ID_9304 Human_SNP_ID_5671802 A-to-I Human chr1 - 21137734 21137734 21137734 CTCACTGCAGCCTTGACCACCAGGCTCAAGTGATCCTCCCACTTCAGCTTCCTGAGTAGCTGGGA CTCACTGCAGCCTTGACCACCAGGCTCAAGTGGTCCTCCCACTTCAGCTTCCTGAGTAGCTGGGA T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917176674 Functional Loss SNV dbSNP153 33..33 33 - - - 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 9305 RMVar_ID_9305 Human_SNP_ID_5672265 A-to-I Human chr1 - 21139724 21139724 21139724 TAAATAGCCACTGCACTCTAAGTTGGCAACATAGTGAAACCCATCTTAAAAAAAATTAAATAGAT TAAATAGCCACTGCACTCTAAGTTGGCAACATGGTGAAACCCATCTTAAAAAAAATTAAATAGAT T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1384834845 Functional Loss SNV dbSNP153 33..33 33 - - - 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 9306 RMVar_ID_9306 Human_SNP_ID_5672297 A-to-I Human chr1 - 21139839 21139839 21139839 AGTTTAAATTATATAGACCAGTGTGGGCCTGTAGTCCTAGCTACTCGGGAGGCTGAAGCAGGAGT AGTTTAAATTATATAGACCAGTGTGGGCCTGTGGTCCTAGCTACTCGGGAGGCTGAAGCAGGAGT T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1038801292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10766947,Human_RBP_ID_22562445 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 9307 RMVar_ID_9307 Human_SNP_ID_5672778 A-to-I Human chr1 - 21141830 21141830 21141830 ATTTCCCAGGCTCAAGCGATTCTTCCCCTTCAACCTCTCTAGTAGCTGGGACTACAGGCCCACAC ATTTCCCAGGCTCAAGCGATTCTTCCCCTTCAGCCTCTCTAGTAGCTGGGACTACAGGCCCACAC T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1005513374 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5753824 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 9308 RMVar_ID_9308 Human_SNP_ID_5672779 A-to-I Human chr1 - 21141830 21141830 21141830 ATTTCCCAGGCTCAAGCGATTCTTCCCCTTCAACCTCTCTAGTAGCTGGGACTACAGGCCCACAC ATTTCCCAGGCTCAAGCGATTCTTCCCCTTCACCCTCTCTAGTAGCTGGGACTACAGGCCCACAC T G EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1005513374 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5753824 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 9309 RMVar_ID_9309 Human_SNP_ID_5672784 A-to-I Human chr1 - 21141855 21141855 21141855 ATAATCACAGCTCACTGCAGCGTCGATTTCCCAGGCTCAAGCGATTCTTCCCCTTCAACCTCTCT ATAATCACAGCTCACTGCAGCGTCGATTTCCCGGGCTCAAGCGATTCTTCCCCTTCAACCTCTCT T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1336162440 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18562325 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 9310 RMVar_ID_9310 Human_SNP_ID_5672938 A-to-I Human chr1 - 21142431 21142431 21142431 ACGATCTCAACTCACTGCAACTTCCACCATCCAGGCTCAAGCGATCCTCCTACCTCAGCCTCCTG ACGATCTCAACTCACTGCAACTTCCACCATCCGGGCTCAAGCGATCCTCCTACCTCAGCCTCCTG T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965058679 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_95823 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 9311 RMVar_ID_9311 Human_SNP_ID_5673258 A-to-I Human chr1 - 21143727 21143727 21143727 TTTAGTAGAGATGGGGTTTTGCCATGTTGGCCAGCCTGGTCCCAAACTCCTGGCCTCAAGTGATT TTTAGTAGAGATGGGGTTTTGCCATGTTGGCCGGCCTGGTCCCAAACTCCTGGCCTCAAGTGATT T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs545897097 Functional Loss SNV dbSNP153 33..33 33 - - - 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 9312 RMVar_ID_9312 Human_SNP_ID_5674321 A-to-I Human chr1 - 21148290 21148290 21148290 AAGGTAGGCAGATTGTTTAGACCCGGGAGTTCAAGACCAACCTGGGCAACATAGCAAGACCTTGT AAGGTAGGCAGATTGTTTAGACCCGGGAGTTCGAGACCAACCTGGGCAACATAGCAAGACCTTGT T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1180048045 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557025 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 9313 RMVar_ID_9313 Human_SNP_ID_5674959 A-to-I Human chr1 - 21150751 21150751 21150751 GCTGATCTCGAACTCCCGACCTCAGGTGGTCCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTAC GCTGATCTCGAACTCCCGACCTCAGGTGGTCCCCCCGCCTCGGCCTCCCAAAGTGCTGGGATTAC T G EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs976873959 Functional Loss SNV dbSNP153 33..33 33 - - - 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 9314 RMVar_ID_9314 Human_SNP_ID_5675374 A-to-I Human chr1 - 21152250 21152250 21152250 TCACTGCAGCACTGACCTTCCAGGCTCAAGCAATCCACCTGCCTTTGCCTCCCAAAGTCTTGGGA TCACTGCAGCACTGACCTTCCAGGCTCAAGCAGTCCACCTGCCTTTGCCTCCCAAAGTCTTGGGA T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs563518886 Functional Loss SNV dbSNP153 33..33 33 - - - 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 9315 RMVar_ID_9315 Human_SNP_ID_5676915 A-to-I Human chr1 - 21158273 21158273 21158273 CACTCAGGAGGCTGAGGTGGGTGGATTGCTTGAGTCCGTGAGGTGGAGGCTGCAGTGAGTGGAGA CACTCAGGAGGCTGAGGTGGGTGGATTGCTTGTGTCCGTGAGGTGGAGGCTGCAGTGAGTGGAGA T A EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1262796225 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557028 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 9316 RMVar_ID_9316 Human_SNP_ID_5676947 A-to-I Human chr1 - 21158426 21158426 21158426 CACACCTGTAATTCTAACACTTTGAGAGGCCAAGGTGGGTGGATTGCTTGAGCTTAGGAGTTTGA CACACCTGTAATTCTAACACTTTGAGAGGCCAGGGTGGGTGGATTGCTTGAGCTTAGGAGTTTGA T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs532102951 Functional Loss SNV dbSNP153 33..33 33 - - - 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 9317 RMVar_ID_9317 Human_SNP_ID_5677010 A-to-I Human chr1 - 21158690 21158690 21158690 GTGTATACTCACCGTTGGACTCAAACTCAGGTAATTCTACTGCCTCAGCTTCTTGAGTAGGGGGG GTGTATACTCACCGTTGGACTCAAACTCAGGTGATTCTACTGCCTCAGCTTCTTGAGTAGGGGGG T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1433597718 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1074948,Human_RBP_ID_1252766,Human_RBP_ID_2122146,Human_RBP_ID_9485932,Human_RBP_ID_17181481,Human_RBP_ID_17738586,Human_RBP_ID_23363094 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 9318 RMVar_ID_9318 Human_SNP_ID_5677379 A-to-I Human chr1 - 21160044 21160044 21160044 GGAGTGCAATAGCACAATTTCGGCTCACTGCAACCTCTGCCTCCCAGGTTCAAGCGATTAGCTTG GGAGTGCAATAGCACAATTTCGGCTCACTGCACCCTCTGCCTCCCAGGTTCAAGCGATTAGCTTG T G EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1463699775 Functional Loss SNV dbSNP153 33..33 33 - - - 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 9319 RMVar_ID_9319 Human_SNP_ID_5678036 A-to-I Human chr1 - 21162386 21162386 21162386 GGAGTGCTGTGGTGTGATCTCAGTTCACTGCAACGTCCACCTCCTGGGTTCAAATGATTCTCCTG GGAGTGCTGTGGTGTGATCTCAGTTCACTGCACCGTCCACCTCCTGGGTTCAAATGATTCTCCTG T G EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs926100576 Functional Loss SNV dbSNP153 33..33 33 - - - 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 9320 RMVar_ID_9320 Human_SNP_ID_5678063 A-to-I Human chr1 - 21162448 21162448 21162448 GCCACTGTGTCCCACCTTTTTTTTTTTTTTTTAAGATGATGTCTTGCTCTGTTGCCCAGGCTGGA GCCACTGTGTCCCACCTTTTTTTTTTTTTTTTTAGATGATGTCTTGCTCTGTTGCCCAGGCTGGA T A EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1441274294 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9485989,Human_RBP_ID_10770564,Human_RBP_ID_23146770,Human_RBP_ID_23363137,Human_RBP_ID_24635626 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 9321 RMVar_ID_9321 Human_SNP_ID_5678064 A-to-I Human chr1 - 21162448 21162448 21162448 GCCACTGTGTCCCACCTTTTTTTTTTTTTTTTAAGATGATGTCTTGCTCTGTTGCCCAGGCTGGA GCCACTGTGTCCCACCTTTTTTTTTTTTTTTTCAGATGATGTCTTGCTCTGTTGCCCAGGCTGGA T G EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1441274294 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9485989,Human_RBP_ID_10770564,Human_RBP_ID_23146770,Human_RBP_ID_23363137,Human_RBP_ID_24635626 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 9322 RMVar_ID_9322 Human_SNP_ID_5678566 A-to-I Human chr1 - 21164642 21164642 21164642 TTGCCCAGGCTGGTCTCCAACTCCTGGGCTCAAGTGATCTGCCTACCTTTGCCTTCCAAAATGCG TTGCCCAGGCTGGTCTCCAACTCCTGGGCTCAGGTGATCTGCCTACCTTTGCCTTCCAAAATGCG T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1235557968 Functional Loss SNV dbSNP153 33..33 33 - - - 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 9323 RMVar_ID_9323 Human_SNP_ID_5679227 A-to-I Human chr1 - 21167072 21167072 21167072 ATAGAACTTGGTCGGAGAACTTGGCCAGGTGCAGTGACTCATGGCCTGTAATCCCAGCACTTCAG ATAGAACTTGGTCGGAGAACTTGGCCAGGTGCGGTGACTCATGGCCTGTAATCCCAGCACTTCAG T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs756730633 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10770970 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_130024 9324 RMVar_ID_9324 Human_SNP_ID_5679357 A-to-I Human chr1 - 21167573 21167573 21167573 TTGTATTTTTAGTTGAGGCAGGGTTTCACCATATTGGCCTGGCTGGTCTTGAACTCCTGACCTTG TTGTATTTTTAGTTGAGGCAGGGTTTCACCATGTTGGCCTGGCTGGTCTTGAACTCCTGACCTTG T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1490796599 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4023896,Human_RBP_ID_10771016,Human_RBP_ID_24635700 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_130024 9325 RMVar_ID_9325 Human_SNP_ID_5679629 A-to-I Human chr1 - 21168547 21168547 21168547 GTGGCAGTGCATGCCTGTAGTCCCTGCTACTCAGGAGGCTGAGGCCGGAGGATTGCTTGAGCCCG GTGGCAGTGCATGCCTGTAGTCCCTGCTACTCGGGAGGCTGAGGCCGGAGGATTGCTTGAGCCCG T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1271443074 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10771056,Human_RBP_ID_22707949 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_130024 9326 RMVar_ID_9326 Human_SNP_ID_5680848 A-to-I Human chr1 - 21173272 21173272 21173272 GAATCGCTTGAACCCACGAGGCAGAAGTTGCAATGAGCCGAGACTGCACCACTGCGCTCCAGCCT GAATCGCTTGAACCCACGAGGCAGAAGTTGCAGTGAGCCGAGACTGCACCACTGCGCTCCAGCCT T C EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1373851169 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10771238 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_130012,RMVar_hsa_circ_130010 9327 RMVar_ID_9327 Human_SNP_ID_5680862 A-to-I Human chr1 - 21173308 21173308 21173308 CCTGTAATTTCAGCTACTCAGGAGGCCAAGGCAGGAGAATCGCTTGAACCCACGAGGCAGAAGTT CCTGTAATTTCAGCTACTCAGGAGGCCAAGGCCGGAGAATCGCTTGAACCCACGAGGCAGAAGTT T G EIF4G3 Ensembl:ENSG00000075151 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1475006127 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10771240 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_130012,RMVar_hsa_circ_130010 9328 RMVar_ID_9328 Human_SNP_ID_5693587 A-to-I Human chr1 - 21220640 21220640 21220640 GGCACGCACCACCACGCCCATCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTTG GGCACGCACCACCACGCCCATCTAATTTTTGTGTTTTTAGTAGAGACAGGGTTTCACCATGTTTG T C ECE1 Ensembl:ENSG00000117298 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1257326899 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23363280 9329 RMVar_ID_9329 Human_SNP_ID_5694021 A-to-I Human chr1 - 21222534 21222534 21222534 ACCCGGCCATGTGGCTGCTTTCATGCTGCAATAGCAGAATTGAGTCATTGCAGCGGTGACCATTA ACCCGGCCATGTGGCTGCTTTCATGCTGCAATGGCAGAATTGAGTCATTGCAGCGGTGACCATTA T C ECE1 Ensembl:ENSG00000117298 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1194666833 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92267,RMVar_hsa_circ_338823,RMVar_hsa_circ_279800,RMVar_hsa_circ_130028,RMVar_hsa_circ_17147,RMVar_hsa_circ_130027 9330 RMVar_ID_9330 Human_SNP_ID_5694048 A-to-I Human chr1 - 21222638 21222638 21222638 TGGGGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTCCTAACCTCAGGTGATCCACCTGCCTGG TGGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTAACCTCAGGTGATCCACCTGCCTGG T C ECE1 Ensembl:ENSG00000117298 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1182748789 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92267,RMVar_hsa_circ_338823,RMVar_hsa_circ_279800,RMVar_hsa_circ_130028,RMVar_hsa_circ_17147,RMVar_hsa_circ_130027 9331 RMVar_ID_9331 Human_SNP_ID_5695596 A-to-I Human chr1 - 21228713 21228713 21228713 TCAATCTCAGCTCACTGCAACCTCCACCTCCCAGGTTTAAGCAATTCTCGTGCCTCAGCCACCCA TCAATCTCAGCTCACTGCAACCTCCACCTCCCGGGTTTAAGCAATTCTCGTGCCTCAGCCACCCA T C ECE1 Ensembl:ENSG00000117298 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1383906641 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9887,RMVar_hsa_circ_92267,RMVar_hsa_circ_130028,RMVar_hsa_circ_17147 9332 RMVar_ID_9332 Human_SNP_ID_5700097 A-to-I Human chr1 - 21246820 21246820 21246820 ACGGTGTCTCTACAAAAAATAAAAAATTAGCCAGACATGGTGTCGCGTGCCTGTCACCCAGCTCC ACGGTGTCTCTACAAAAAATAAAAAATTAGCCGGACATGGTGTCGCGTGCCTGTCACCCAGCTCC T C ECE1 Ensembl:ENSG00000117298 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1019294277 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92267,RMVar_hsa_circ_130028,RMVar_hsa_circ_363958,RMVar_hsa_circ_42002,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_273940,RMVar_hsa_circ_70604,RMVar_hsa_circ_130036,RMVar_hsa_circ_130037,RMVar_hsa_circ_130035 9333 RMVar_ID_9333 Human_SNP_ID_5700100 A-to-I Human chr1 - 21246824 21246824 21246824 CGAGACGGTGTCTCTACAAAAAATAAAAAATTAGCCAGACATGGTGTCGCGTGCCTGTCACCCAG CGAGACGGTGTCTCTACAAAAAATAAAAAATTGGCCAGACATGGTGTCGCGTGCCTGTCACCCAG T C ECE1 Ensembl:ENSG00000117298 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965092609 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92267,RMVar_hsa_circ_130028,RMVar_hsa_circ_363958,RMVar_hsa_circ_42002,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_273940,RMVar_hsa_circ_70604,RMVar_hsa_circ_130036,RMVar_hsa_circ_130037,RMVar_hsa_circ_130035 9334 RMVar_ID_9334 Human_SNP_ID_5707681 A-to-I Human chr1 - 21276150 21276150 21276150 GTGGTGTTGGATGCCTGTAATCCTAGCTACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAATCCA GTGGTGTTGGATGCCTGTAATCCTAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCTTGAATCCA T C ECE1 Ensembl:ENSG00000117298 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1304042791 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28078,RMVar_hsa_circ_75714,RMVar_hsa_circ_378812,RMVar_hsa_circ_130033,RMVar_hsa_circ_45849,RMVar_hsa_circ_79971,RMVar_hsa_circ_18575,RMVar_hsa_circ_39611,RMVar_hsa_circ_358653,RMVar_hsa_circ_325610,RMVar_hsa_circ_271455,RMVar_hsa_circ_130043,RMVar_hsa_circ_130044,RMVar_hsa_circ_130042 9335 RMVar_ID_9335 Human_SNP_ID_5707694 A-to-I Human chr1 - 21276199 21276199 21276199 CAACATGGTGAAACCTCGTGTCTACTAAAAATACAAAAATTAGCCAGGCGTGGTGTTGGATGCCT CAACATGGTGAAACCTCGTGTCTACTAAAAATGCAAAAATTAGCCAGGCGTGGTGTTGGATGCCT T C ECE1 Ensembl:ENSG00000117298 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs980473353 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28078,RMVar_hsa_circ_75714,RMVar_hsa_circ_378812,RMVar_hsa_circ_130033,RMVar_hsa_circ_45849,RMVar_hsa_circ_79971,RMVar_hsa_circ_18575,RMVar_hsa_circ_39611,RMVar_hsa_circ_358653,RMVar_hsa_circ_325610,RMVar_hsa_circ_271455,RMVar_hsa_circ_130043,RMVar_hsa_circ_130044,RMVar_hsa_circ_130042 9336 RMVar_ID_9336 Human_SNP_ID_5707695 A-to-I Human chr1 - 21276201 21276201 21276201 GCCAACATGGTGAAACCTCGTGTCTACTAAAAATACAAAAATTAGCCAGGCGTGGTGTTGGATGC GCCAACATGGTGAAACCTCGTGTCTACTAAAAGTACAAAAATTAGCCAGGCGTGGTGTTGGATGC T C ECE1 Ensembl:ENSG00000117298 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1028187877 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28078,RMVar_hsa_circ_75714,RMVar_hsa_circ_378812,RMVar_hsa_circ_130033,RMVar_hsa_circ_45849,RMVar_hsa_circ_79971,RMVar_hsa_circ_18575,RMVar_hsa_circ_39611,RMVar_hsa_circ_358653,RMVar_hsa_circ_325610,RMVar_hsa_circ_271455,RMVar_hsa_circ_130043,RMVar_hsa_circ_130044,RMVar_hsa_circ_130042 9337 RMVar_ID_9337 Human_SNP_ID_5707704 A-to-I Human chr1 - 21276245 21276245 21276245 GAGGCGGGTGGATCACCTGAGGTCAAGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCTCGT GAGGCGGGTGGATCACCTGAGGTCAAGAGTTCCAGACCAGCCTGGCCAACATGGTGAAACCTCGT T G ECE1 Ensembl:ENSG00000117298 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1276507946 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28078,RMVar_hsa_circ_75714,RMVar_hsa_circ_378812,RMVar_hsa_circ_130033,RMVar_hsa_circ_45849,RMVar_hsa_circ_79971,RMVar_hsa_circ_18575,RMVar_hsa_circ_39611,RMVar_hsa_circ_358653,RMVar_hsa_circ_325610,RMVar_hsa_circ_271455,RMVar_hsa_circ_130043,RMVar_hsa_circ_130044,RMVar_hsa_circ_130042 9338 RMVar_ID_9338 Human_SNP_ID_5707705 A-to-I Human chr1 - 21276252 21276252 21276252 GGAGGCCGAGGCGGGTGGATCACCTGAGGTCAAGAGTTCAAGACCAGCCTGGCCAACATGGTGAA GGAGGCCGAGGCGGGTGGATCACCTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGGTGAA T C ECE1 Ensembl:ENSG00000117298 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs989250279 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28078,RMVar_hsa_circ_75714,RMVar_hsa_circ_378812,RMVar_hsa_circ_130033,RMVar_hsa_circ_45849,RMVar_hsa_circ_79971,RMVar_hsa_circ_18575,RMVar_hsa_circ_39611,RMVar_hsa_circ_358653,RMVar_hsa_circ_325610,RMVar_hsa_circ_271455,RMVar_hsa_circ_130043,RMVar_hsa_circ_130044,RMVar_hsa_circ_130042 9339 RMVar_ID_9339 Human_SNP_ID_5720848 A-to-I Human chr1 - 21330338 21330338 21330338 TTTGGTCCCAGCTACTCAGGAGGCTGAGAATCACTTGAACCCGGGAGGCAGAGGTTGCAGTGAGT TTTGGTCCCAGCTACTCAGGAGGCTGAGAATCGCTTGAACCCGGGAGGCAGAGGTTGCAGTGAGT T C ECE1 Ensembl:ENSG00000117298 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1412853369 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125447,RMVar_hsa_circ_130047 9340 RMVar_ID_9340 Human_SNP_ID_5720999 A-to-I Human chr1 - 21331031 21331030 21331032 GCTCAAGCGATCGTCCTGCCTCGGACCCCCAAAGTTTGGGATGACAGGCGTGAACCACCACCCCT GCTCAAGCGATCGTCCTGCCTCGGACCCCCA__GTTTGGGATGACAGGCGTGAACCACCACCCCT CTT C ECE1 Ensembl:ENSG00000117298 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256655956 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_125447,RMVar_hsa_circ_130047 9341 RMVar_ID_9341 Human_SNP_ID_5721096 A-to-I Human chr1 - 21331342 21331342 21331342 TGGAGTGCAGTGGCATGATCTCGGCTCATTGCAATTGTCACCTCCTGGGTTCAAGCGATTCCTCT TGGAGTGCAGTGGCATGATCTCGGCTCATTGCCATTGTCACCTCCTGGGTTCAAGCGATTCCTCT T G ECE1 Ensembl:ENSG00000117298 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs980836516 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125447,RMVar_hsa_circ_130047 9342 RMVar_ID_9342 Human_SNP_ID_5745691 A-to-I Human chr1 - 21423637 21423637 21423637 ATCTTTTTGTTGTTGTCATTGATTGTGGTGACATGGACTTATTTGTAGAGGACAGGTCAGCTGTC ATCTTTTTGTTGTTGTCATTGATTGTGGTGACGTGGACTTATTTGTAGAGGACAGGTCAGCTGTC T C lnc-ECE1-2 RNACentral:URS0000D5A309 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1414145534 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108762,RMVar_hsa_circ_130049,RMVar_hsa_circ_103959,RMVar_hsa_circ_130048 9343 RMVar_ID_9343 Human_SNP_ID_5812980 A-to-I Human chr1 - 21685440 21685440 21685440 CGTAGTAGCGCATGCCTGTAATCCCAGTTACTAGGGAGGCTGAGGCAGGAGAATTGCTTGAACCC CGTAGTAGCGCATGCCTGTAATCCCAGTTACTGGGGAGGCTGAGGCAGGAGAATTGCTTGAACCC T C USP48 Ensembl:ENSG00000090686 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1203143095 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4386,RMVar_hsa_circ_116760,RMVar_hsa_circ_316555,RMVar_hsa_circ_285129,RMVar_hsa_circ_46563,RMVar_hsa_circ_130061,RMVar_hsa_circ_130063,RMVar_hsa_circ_130064,RMVar_hsa_circ_130062 9344 RMVar_ID_9344 Human_SNP_ID_5813112 A-to-I Human chr1 - 21685872 21685872 21685872 CCCCCTGTGATCTGGCCACCTGGGCCTCCCAAAATGCTAGAATTACAGGCATGAGCCACCATGCC CCCCCTGTGATCTGGCCACCTGGGCCTCCCAAGATGCTAGAATTACAGGCATGAGCCACCATGCC T C USP48 Ensembl:ENSG00000090686 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs890576749 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4386,RMVar_hsa_circ_116760,RMVar_hsa_circ_316555,RMVar_hsa_circ_285129,RMVar_hsa_circ_46563,RMVar_hsa_circ_130061,RMVar_hsa_circ_130063,RMVar_hsa_circ_130064,RMVar_hsa_circ_130062 9345 RMVar_ID_9345 Human_SNP_ID_5813132 A-to-I Human chr1 - 21685949 21685949 21685949 TGACACCCAGCTAATTTTTGTATTTTTACTAGAGATGAGGATTTCCCATATTGGCCAGGCTGGTC TGACACCCAGCTAATTTTTGTATTTTTACTAGGGATGAGGATTTCCCATATTGGCCAGGCTGGTC T C USP48 Ensembl:ENSG00000090686 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1373889476 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4386,RMVar_hsa_circ_116760,RMVar_hsa_circ_316555,RMVar_hsa_circ_285129,RMVar_hsa_circ_46563,RMVar_hsa_circ_130061,RMVar_hsa_circ_130063,RMVar_hsa_circ_130064,RMVar_hsa_circ_130062,RMVar_hsa_circ_130065,RMVar_hsa_circ_99821 9346 RMVar_ID_9346 Human_SNP_ID_5814351 A-to-I Human chr1 - 21690824 21690824 21690824 TTAAAGATGGTTTTAAGAAAGAATTTTGGGCCAGATGCAGTGGCTCATGCCTGTAATCTCTGCAC TTAAAGATGGTTTTAAGAAAGAATTTTGGGCCCGATGCAGTGGCTCATGCCTGTAATCTCTGCAC T G USP48 Ensembl:ENSG00000090686 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1409511570 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11197197 RMVar_hsa_circ_5571,RMVar_hsa_circ_115281,RMVar_hsa_circ_4386,RMVar_hsa_circ_116760,RMVar_hsa_circ_316555,RMVar_hsa_circ_285129,RMVar_hsa_circ_46563,RMVar_hsa_circ_130061,RMVar_hsa_circ_130063,RMVar_hsa_circ_130064,RMVar_hsa_circ_130062,RMVar_hsa_circ_292690,RMVar_hsa_circ_130067,RMVar_hsa_circ_60496,RMVar_hsa_circ_105876,RMVar_hsa_circ_130068,RMVar_hsa_circ_113482,RMVar_hsa_circ_267406,RMVar_hsa_circ_325977,RMVar_hsa_circ_130066,RMVar_hsa_circ_290969,RMVar_hsa_circ_266683,RMVar_hsa_circ_25679,RMVar_hsa_circ_130070,RMVar_hsa_circ_130072,RMVar_hsa_circ_130073,RMVar_hsa_circ_130071,RMVar_hsa_circ_130069 9347 RMVar_ID_9347 Human_SNP_ID_5814397 A-to-I Human chr1 - 21691072 21691072 21691072 GACGTGAGGTGATCCGTCCACCTCGGCCTCCCAAAGTGTTGGGATTACAGGCGAGAGCCACTGCA GACGTGAGGTGATCCGTCCACCTCGGCCTCCCGAAGTGTTGGGATTACAGGCGAGAGCCACTGCA T C USP48 Ensembl:ENSG00000090686 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878964613 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5571,RMVar_hsa_circ_115281,RMVar_hsa_circ_4386,RMVar_hsa_circ_116760,RMVar_hsa_circ_316555,RMVar_hsa_circ_285129,RMVar_hsa_circ_46563,RMVar_hsa_circ_130061,RMVar_hsa_circ_130063,RMVar_hsa_circ_130064,RMVar_hsa_circ_130062,RMVar_hsa_circ_292690,RMVar_hsa_circ_130067,RMVar_hsa_circ_60496,RMVar_hsa_circ_105876,RMVar_hsa_circ_130068,RMVar_hsa_circ_113482,RMVar_hsa_circ_267406,RMVar_hsa_circ_325977,RMVar_hsa_circ_130066,RMVar_hsa_circ_290969,RMVar_hsa_circ_266683,RMVar_hsa_circ_25679,RMVar_hsa_circ_130070,RMVar_hsa_circ_130072,RMVar_hsa_circ_130073,RMVar_hsa_circ_130071,RMVar_hsa_circ_130069 9348 RMVar_ID_9348 Human_SNP_ID_5814526 A-to-I Human chr1 - 21691552 21691552 21691552 CGGCTTACTGCAACTTCTGCTTCCTGGGTTCAAGTGATTCTCCTCCCTCAGCCTCCCAAGTAGCT CGGCTTACTGCAACTTCTGCTTCCTGGGTTCACGTGATTCTCCTCCCTCAGCCTCCCAAGTAGCT T G USP48 Ensembl:ENSG00000090686 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909362759 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5571,RMVar_hsa_circ_115281,RMVar_hsa_circ_4386,RMVar_hsa_circ_116760,RMVar_hsa_circ_316555,RMVar_hsa_circ_285129,RMVar_hsa_circ_46563,RMVar_hsa_circ_130061,RMVar_hsa_circ_130063,RMVar_hsa_circ_130064,RMVar_hsa_circ_130062,RMVar_hsa_circ_292690,RMVar_hsa_circ_130067,RMVar_hsa_circ_60496,RMVar_hsa_circ_105876,RMVar_hsa_circ_130068,RMVar_hsa_circ_113482,RMVar_hsa_circ_267406,RMVar_hsa_circ_325977,RMVar_hsa_circ_130066,RMVar_hsa_circ_290969,RMVar_hsa_circ_266683,RMVar_hsa_circ_25679,RMVar_hsa_circ_130070,RMVar_hsa_circ_130072,RMVar_hsa_circ_130073,RMVar_hsa_circ_130071,RMVar_hsa_circ_130069 9349 RMVar_ID_9349 Human_SNP_ID_5818960 A-to-I Human chr1 - 21708802 21708802 21708802 TGGCTCACTGCAACCTCTGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCATGTAGCT TGGCTCACTGCAACCTCTGCCTCCCGGGTTCAGGCGATTCTCCTGCCTCAGCCTCCCATGTAGCT T C USP48 Ensembl:ENSG00000090686 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs982273372 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61016,RMVar_hsa_circ_5571,RMVar_hsa_circ_115281,RMVar_hsa_circ_4386,RMVar_hsa_circ_116760,RMVar_hsa_circ_316555,RMVar_hsa_circ_130061,RMVar_hsa_circ_130063,RMVar_hsa_circ_130062,RMVar_hsa_circ_130067,RMVar_hsa_circ_105876,RMVar_hsa_circ_130068,RMVar_hsa_circ_113482,RMVar_hsa_circ_325977,RMVar_hsa_circ_25679,RMVar_hsa_circ_130072,RMVar_hsa_circ_130073,RMVar_hsa_circ_130071,RMVar_hsa_circ_344549,RMVar_hsa_circ_312993,RMVar_hsa_circ_27088,RMVar_hsa_circ_337136,RMVar_hsa_circ_351931,RMVar_hsa_circ_130074,RMVar_hsa_circ_351774,RMVar_hsa_circ_326515,RMVar_hsa_circ_5706,RMVar_hsa_circ_53512,RMVar_hsa_circ_54323,RMVar_hsa_circ_130079,RMVar_hsa_circ_130080,RMVar_hsa_circ_328004,RMVar_hsa_circ_362605,RMVar_hsa_circ_339341,RMVar_hsa_circ_18267,RMVar_hsa_circ_49375,RMVar_hsa_circ_130082,RMVar_hsa_circ_130083,RMVar_hsa_circ_130081,RMVar_hsa_circ_29044,RMVar_hsa_circ_54132,RMVar_hsa_circ_130085,RMVar_hsa_circ_94140,RMVar_hsa_circ_375851,RMVar_hsa_circ_130084,RMVar_hsa_circ_269122,RMVar_hsa_circ_378450 9350 RMVar_ID_9350 Human_SNP_ID_5818961 A-to-I Human chr1 - 21708802 21708802 21708802 TGGCTCACTGCAACCTCTGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCATGTAGCT TGGCTCACTGCAACCTCTGCCTCCCGGGTTCACGCGATTCTCCTGCCTCAGCCTCCCATGTAGCT T G USP48 Ensembl:ENSG00000090686 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs982273372 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61016,RMVar_hsa_circ_5571,RMVar_hsa_circ_115281,RMVar_hsa_circ_4386,RMVar_hsa_circ_116760,RMVar_hsa_circ_316555,RMVar_hsa_circ_130061,RMVar_hsa_circ_130063,RMVar_hsa_circ_130062,RMVar_hsa_circ_130067,RMVar_hsa_circ_105876,RMVar_hsa_circ_130068,RMVar_hsa_circ_113482,RMVar_hsa_circ_325977,RMVar_hsa_circ_25679,RMVar_hsa_circ_130072,RMVar_hsa_circ_130073,RMVar_hsa_circ_130071,RMVar_hsa_circ_344549,RMVar_hsa_circ_312993,RMVar_hsa_circ_27088,RMVar_hsa_circ_337136,RMVar_hsa_circ_351931,RMVar_hsa_circ_130074,RMVar_hsa_circ_351774,RMVar_hsa_circ_326515,RMVar_hsa_circ_5706,RMVar_hsa_circ_53512,RMVar_hsa_circ_54323,RMVar_hsa_circ_130079,RMVar_hsa_circ_130080,RMVar_hsa_circ_328004,RMVar_hsa_circ_362605,RMVar_hsa_circ_339341,RMVar_hsa_circ_18267,RMVar_hsa_circ_49375,RMVar_hsa_circ_130082,RMVar_hsa_circ_130083,RMVar_hsa_circ_130081,RMVar_hsa_circ_29044,RMVar_hsa_circ_54132,RMVar_hsa_circ_130085,RMVar_hsa_circ_94140,RMVar_hsa_circ_375851,RMVar_hsa_circ_130084,RMVar_hsa_circ_269122,RMVar_hsa_circ_378450 9351 RMVar_ID_9351 Human_SNP_ID_5819096 A-to-I Human chr1 - 21709034 21709034 21709034 ATGGTGGCTCATGCCTGTTAGCCAGACTACTCAGGAGGCTAAGGCAGGAGGATCGCTTGAGCCCA ATGGTGGCTCATGCCTGTTAGCCAGACTACTCCGGAGGCTAAGGCAGGAGGATCGCTTGAGCCCA T G USP48 Ensembl:ENSG00000090686 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs900461783 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5758635 RMVar_hsa_circ_61016,RMVar_hsa_circ_5571,RMVar_hsa_circ_115281,RMVar_hsa_circ_4386,RMVar_hsa_circ_116760,RMVar_hsa_circ_316555,RMVar_hsa_circ_130061,RMVar_hsa_circ_130063,RMVar_hsa_circ_130062,RMVar_hsa_circ_130067,RMVar_hsa_circ_105876,RMVar_hsa_circ_130068,RMVar_hsa_circ_113482,RMVar_hsa_circ_325977,RMVar_hsa_circ_25679,RMVar_hsa_circ_130072,RMVar_hsa_circ_130073,RMVar_hsa_circ_130071,RMVar_hsa_circ_344549,RMVar_hsa_circ_312993,RMVar_hsa_circ_27088,RMVar_hsa_circ_337136,RMVar_hsa_circ_351931,RMVar_hsa_circ_130074,RMVar_hsa_circ_351774,RMVar_hsa_circ_326515,RMVar_hsa_circ_5706,RMVar_hsa_circ_53512,RMVar_hsa_circ_54323,RMVar_hsa_circ_130079,RMVar_hsa_circ_130080,RMVar_hsa_circ_328004,RMVar_hsa_circ_362605,RMVar_hsa_circ_339341,RMVar_hsa_circ_18267,RMVar_hsa_circ_49375,RMVar_hsa_circ_130082,RMVar_hsa_circ_130083,RMVar_hsa_circ_130081,RMVar_hsa_circ_29044,RMVar_hsa_circ_54132,RMVar_hsa_circ_130085,RMVar_hsa_circ_94140,RMVar_hsa_circ_375851,RMVar_hsa_circ_130084,RMVar_hsa_circ_269122,RMVar_hsa_circ_378450 9352 RMVar_ID_9352 Human_SNP_ID_5819925 A-to-I Human chr1 - 21712721 21712721 21712721 GGGAGGCTGACCCAGGAGAATTGCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCCAAGATGGCA GGGAGGCTGACCCAGGAGAATTGCTTGAACCCGGGAGGCGGAGGTTGCAGTGAGCCAAGATGGCA T C USP48 Ensembl:ENSG00000090686 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs542550788 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61016,RMVar_hsa_circ_5571,RMVar_hsa_circ_115281,RMVar_hsa_circ_4386,RMVar_hsa_circ_116760,RMVar_hsa_circ_316555,RMVar_hsa_circ_130061,RMVar_hsa_circ_130063,RMVar_hsa_circ_130062,RMVar_hsa_circ_130067,RMVar_hsa_circ_105876,RMVar_hsa_circ_130068,RMVar_hsa_circ_113482,RMVar_hsa_circ_325977,RMVar_hsa_circ_25679,RMVar_hsa_circ_130072,RMVar_hsa_circ_130073,RMVar_hsa_circ_130071,RMVar_hsa_circ_344549,RMVar_hsa_circ_312993,RMVar_hsa_circ_27088,RMVar_hsa_circ_337136,RMVar_hsa_circ_351931,RMVar_hsa_circ_130074,RMVar_hsa_circ_351774,RMVar_hsa_circ_326515,RMVar_hsa_circ_5706,RMVar_hsa_circ_53512,RMVar_hsa_circ_54323,RMVar_hsa_circ_130079,RMVar_hsa_circ_130080,RMVar_hsa_circ_328004,RMVar_hsa_circ_362605,RMVar_hsa_circ_339341,RMVar_hsa_circ_18267,RMVar_hsa_circ_49375,RMVar_hsa_circ_130082,RMVar_hsa_circ_130083,RMVar_hsa_circ_130081,RMVar_hsa_circ_29044,RMVar_hsa_circ_54132,RMVar_hsa_circ_130085,RMVar_hsa_circ_94140,RMVar_hsa_circ_375851,RMVar_hsa_circ_130084,RMVar_hsa_circ_269122,RMVar_hsa_circ_378450 9353 RMVar_ID_9353 Human_SNP_ID_5819936 A-to-I Human chr1 - 21712766 21712766 21712766 AAATTAGCTGGATGTCATGGTGGACGCCTGTAATCCCACCTACTCGGGAGGCTGACCCAGGAGAA AAATTAGCTGGATGTCATGGTGGACGCCTGTATTCCCACCTACTCGGGAGGCTGACCCAGGAGAA T A USP48 Ensembl:ENSG00000090686 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1424780445 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61016,RMVar_hsa_circ_5571,RMVar_hsa_circ_115281,RMVar_hsa_circ_4386,RMVar_hsa_circ_116760,RMVar_hsa_circ_316555,RMVar_hsa_circ_130061,RMVar_hsa_circ_130063,RMVar_hsa_circ_130062,RMVar_hsa_circ_130067,RMVar_hsa_circ_105876,RMVar_hsa_circ_130068,RMVar_hsa_circ_113482,RMVar_hsa_circ_325977,RMVar_hsa_circ_25679,RMVar_hsa_circ_130072,RMVar_hsa_circ_130073,RMVar_hsa_circ_130071,RMVar_hsa_circ_344549,RMVar_hsa_circ_312993,RMVar_hsa_circ_27088,RMVar_hsa_circ_337136,RMVar_hsa_circ_351931,RMVar_hsa_circ_130074,RMVar_hsa_circ_351774,RMVar_hsa_circ_326515,RMVar_hsa_circ_5706,RMVar_hsa_circ_53512,RMVar_hsa_circ_54323,RMVar_hsa_circ_130079,RMVar_hsa_circ_130080,RMVar_hsa_circ_328004,RMVar_hsa_circ_362605,RMVar_hsa_circ_339341,RMVar_hsa_circ_18267,RMVar_hsa_circ_49375,RMVar_hsa_circ_130082,RMVar_hsa_circ_130083,RMVar_hsa_circ_130081,RMVar_hsa_circ_29044,RMVar_hsa_circ_54132,RMVar_hsa_circ_130085,RMVar_hsa_circ_94140,RMVar_hsa_circ_375851,RMVar_hsa_circ_130084,RMVar_hsa_circ_269122,RMVar_hsa_circ_378450 9354 RMVar_ID_9354 Human_SNP_ID_5820921 A-to-I Human chr1 - 21716861 21716861 21716861 ACCATGCCTGGCTAATTTTTTGTATTTTTAGTAGAGACGAGGTTTCACTGTGTTAGCCAGGATGG ACCATGCCTGGCTAATTTTTTGTATTTTTAGTGGAGACGAGGTTTCACTGTGTTAGCCAGGATGG T C USP48 Ensembl:ENSG00000090686 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1245610079 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61016,RMVar_hsa_circ_5571,RMVar_hsa_circ_115281,RMVar_hsa_circ_4386,RMVar_hsa_circ_116760,RMVar_hsa_circ_316555,RMVar_hsa_circ_130061,RMVar_hsa_circ_130063,RMVar_hsa_circ_130062,RMVar_hsa_circ_130067,RMVar_hsa_circ_105876,RMVar_hsa_circ_130068,RMVar_hsa_circ_113482,RMVar_hsa_circ_325977,RMVar_hsa_circ_25679,RMVar_hsa_circ_130072,RMVar_hsa_circ_130073,RMVar_hsa_circ_130071,RMVar_hsa_circ_344549,RMVar_hsa_circ_312993,RMVar_hsa_circ_27088,RMVar_hsa_circ_337136,RMVar_hsa_circ_351931,RMVar_hsa_circ_130074,RMVar_hsa_circ_351774,RMVar_hsa_circ_326515,RMVar_hsa_circ_5706,RMVar_hsa_circ_54323,RMVar_hsa_circ_130079,RMVar_hsa_circ_130080,RMVar_hsa_circ_328004,RMVar_hsa_circ_339341,RMVar_hsa_circ_18267,RMVar_hsa_circ_49375,RMVar_hsa_circ_130082,RMVar_hsa_circ_130083,RMVar_hsa_circ_130081,RMVar_hsa_circ_29044,RMVar_hsa_circ_14842,RMVar_hsa_circ_54132,RMVar_hsa_circ_130085,RMVar_hsa_circ_94140,RMVar_hsa_circ_375851,RMVar_hsa_circ_130084,RMVar_hsa_circ_269122,RMVar_hsa_circ_307676,RMVar_hsa_circ_333093,RMVar_hsa_circ_356564,RMVar_hsa_circ_130086,RMVar_hsa_circ_378450,RMVar_hsa_circ_378750,RMVar_hsa_circ_341188,RMVar_hsa_circ_311272,RMVar_hsa_circ_279210,RMVar_hsa_circ_307312,RMVar_hsa_circ_47632,RMVar_hsa_circ_130088,RMVar_hsa_circ_130090,RMVar_hsa_circ_130091,RMVar_hsa_circ_130089,RMVar_hsa_circ_130087 9355 RMVar_ID_9355 Human_SNP_ID_5824490 A-to-I Human chr1 - 21731812 21731812 21731812 CAGGCTGCAGTACAGTGGCGTGATCTTGGCTCACTGCAACCTCTGCCTCCTGGGTTCAACTGATT CAGGCTGCAGTACAGTGGCGTGATCTTGGCTCGCTGCAACCTCTGCCTCCTGGGTTCAACTGATT T C USP48 Ensembl:ENSG00000090686 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1226711323 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61016,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_14842,RMVar_hsa_circ_130085,RMVar_hsa_circ_94140,RMVar_hsa_circ_269122,RMVar_hsa_circ_356564,RMVar_hsa_circ_378750,RMVar_hsa_circ_341188,RMVar_hsa_circ_47632,RMVar_hsa_circ_130087,RMVar_hsa_circ_345155,RMVar_hsa_circ_327037,RMVar_hsa_circ_275100,RMVar_hsa_circ_33068,RMVar_hsa_circ_266719,RMVar_hsa_circ_55095,RMVar_hsa_circ_88666,RMVar_hsa_circ_130095,RMVar_hsa_circ_70094,RMVar_hsa_circ_24423,RMVar_hsa_circ_130096,RMVar_hsa_circ_31546,RMVar_hsa_circ_47499,RMVar_hsa_circ_265895,RMVar_hsa_circ_11237 9356 RMVar_ID_9356 Human_SNP_ID_5825575 A-to-I Human chr1 - 21736196 21736196 21736196 ACAGTCATGGCTGACTGCAGCCTAAACCTGCTAGGCTCAAGTGATCTTCCTGCCTCAGCCTTCCC ACAGTCATGGCTGACTGCAGCCTAAACCTGCTGGGCTCAAGTGATCTTCCTGCCTCAGCCTTCCC T C USP48 Ensembl:ENSG00000090686 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1293840048 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5759259,Human_RBP_ID_24639093 RMVar_hsa_circ_61016,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_14842,RMVar_hsa_circ_130085,RMVar_hsa_circ_94140,RMVar_hsa_circ_269122,RMVar_hsa_circ_356564,RMVar_hsa_circ_378750,RMVar_hsa_circ_341188,RMVar_hsa_circ_47632,RMVar_hsa_circ_130087,RMVar_hsa_circ_345155,RMVar_hsa_circ_327037,RMVar_hsa_circ_275100,RMVar_hsa_circ_33068,RMVar_hsa_circ_266719,RMVar_hsa_circ_55095,RMVar_hsa_circ_88666,RMVar_hsa_circ_130095,RMVar_hsa_circ_70094,RMVar_hsa_circ_24423,RMVar_hsa_circ_130096,RMVar_hsa_circ_31546,RMVar_hsa_circ_47499,RMVar_hsa_circ_265895,RMVar_hsa_circ_11237 9357 RMVar_ID_9357 Human_SNP_ID_5828987 A-to-I Human chr1 - 21749802 21749802 21749802 GAACAGTAGTTTGAAACCAGCCTAGGCAACATAGTGATAGACCGTCTTTGCAAAAAATAAAAAAA GAACAGTAGTTTGAAACCAGCCTAGGCAACATGGTGATAGACCGTCTTTGCAAAAAATAAAAAAA T C USP48 Ensembl:ENSG00000090686 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1332575249 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10783183 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 9358 RMVar_ID_9358 Human_SNP_ID_5828998 A-to-I Human chr1 - 21749862 21749862 21749862 GTGGTGGCTCATGTCTATAATCCCAGCACTTTATGAGACTGAGACAGTAGGATCATTTGAGAACA GTGGTGGCTCATGTCTATAATCCCAGCACTTTGTGAGACTGAGACAGTAGGATCATTTGAGAACA T C USP48 Ensembl:ENSG00000090686 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs550287539 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10783183,Human_RBP_ID_23365144 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 9359 RMVar_ID_9359 Human_SNP_ID_5831983 A-to-I Human chr1 - 21761372 21761372 21761372 CCAGCTACTCCAGAGGCTGAGGCTGGAGGATTACTTGAGTCCAGGATGTAGAGGCTGCAGTGAGC CCAGCTACTCCAGAGGCTGAGGCTGGAGGATTCCTTGAGTCCAGGATGTAGAGGCTGCAGTGAGC T G USP48 Ensembl:ENSG00000090686 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1334758579 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10784176 9360 RMVar_ID_9360 Human_SNP_ID_5834590 A-to-I Human chr1 - 21771122 21771122 21771122 TAAAAAATTATTTGTATTTTAGTTGTTTTTTGAGACAGTCTTGCTCTGTCACCTAGGCTGGAGTG TAAAAAATTATTTGTATTTTAGTTGTTTTTTGGGACAGTCTTGCTCTGTCACCTAGGCTGGAGTG T C USP48 Ensembl:ENSG00000090686 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1421678425 Functional Loss SNV dbSNP153 33..33 33 - - - 9361 RMVar_ID_9361 Human_SNP_ID_5835601 A-to-I Human chr1 - 21774677 21774677 21774677 ATTCTTTTTTCGTTTGTTTGTTTTGAGACAGAATCTTGCTCTGTTGCCAGGCTGGAGTACAGTGG ATTCTTTTTTCGTTTGTTTGTTTTGAGACAGAGTCTTGCTCTGTTGCCAGGCTGGAGTACAGTGG T C USP48 Ensembl:ENSG00000090686 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1261611452 Functional Loss SNV dbSNP153 33..33 33 - - - 9362 RMVar_ID_9362 Human_SNP_ID_5835746 A-to-I Human chr1 - 21775192 21775192 21775192 TACACTGGAGACTGAGGTGGGAGGATGGCTTAAGCTTGGGAGGTGGAGGTTGCAGTGAGCCAAGA TACACTGGAGACTGAGGTGGGAGGATGGCTTACGCTTGGGAGGTGGAGGTTGCAGTGAGCCAAGA T G USP48 Ensembl:ENSG00000090686 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs962897771 Functional Loss SNV dbSNP153 33..33 33 - - - 9363 RMVar_ID_9363 Human_SNP_ID_5835830 A-to-I Human chr1 - 21775521 21775521 21775521 GCCACGCACGGTGGCTTACGCCTGTAGTCCCAACACTTTGTTAGGCCGAGGTGGGAGGATTACTT GCCACGCACGGTGGCTTACGCCTGTAGTCCCAGCACTTTGTTAGGCCGAGGTGGGAGGATTACTT T C USP48 Ensembl:ENSG00000090686 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs942585843 Functional Loss SNV dbSNP153 33..33 33 - - - 9364 RMVar_ID_9364 Human_SNP_ID_5835902 A-to-I Human chr1 - 21775826 21775826 21775826 GTTGCTTAGGCTGGTCTCAAACTCCTGGGCTCAAGGGATCTTCCTTCCTCAGCTTCCTGAATAGC GTTGCTTAGGCTGGTCTCAAACTCCTGGGCTCGAGGGATCTTCCTTCCTCAGCTTCCTGAATAGC T C USP48 Ensembl:ENSG00000090686 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1326894226 Functional Loss SNV dbSNP153 33..33 33 - - - 9365 RMVar_ID_9365 Human_SNP_ID_5877583 A-to-I Human chr1 - 21919209 21919209 21919209 GTTGGCCAGGCTGGTCTCAAACTCCCGACCTCAAGTGATCCGCCAGCCTTGGTTGCTCAAAGTGC GTTGGCCAGGCTGGTCTCAAACTCCCGACCTCCAGTGATCCGCCAGCCTTGGTTGCTCAAAGTGC T G HSPG2 Ensembl:ENSG00000142798 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs923007782 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 9366 RMVar_ID_9366 Human_SNP_ID_5877813 A-to-I Human chr1 - 21920134 21920134 21920134 GGGAGGCCAAGGCTGGCGGATCACTCGAGGCCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGA GGGAGGCCAAGGCTGGCGGATCACTCGAGGCCGGGAGTTCGAGACCAGCCTGGCCAACATGGTGA T C HSPG2 Ensembl:ENSG00000142798 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1007666456 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 9367 RMVar_ID_9367 Human_SNP_ID_5878848 A-to-I Human chr1 - 21924338 21924338 21924338 ATTTTCTGGACTTTGAGTTGTGTTGGGCACTTATAGCTTACGAGTCCTGCCTCTCCAACAAGATC ATTTTCTGGACTTTGAGTTGTGTTGGGCACTTGTAGCTTACGAGTCCTGCCTCTCCAACAAGATC T C HSPG2 Ensembl:ENSG00000142798 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1300069799 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 9368 RMVar_ID_9368 Human_SNP_ID_5908218 A-to-I Human chr1 + 22026543 22026543 22026543 GTGATCCACCCGCCTCGGCCTTCCAAAGTGCTAGAAGTATAGGCATGAGCCACTGTGCCTGGCCT GTGATCCACCCGCCTCGGCCTTCCAAAGTGCTTGAAGTATAGGCATGAGCCACTGTGCCTGGCCT A T AL590556.3,LINC00339,CDC42 Ensembl:ENSG00000285959,Ensembl:ENSG00000218510,Ensembl:ENSG00000070831 lincRNA,lincRNA,Protein coding intron,intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1458066463 Functional Loss SNV dbSNP153 33..33 33 - - - 9369 RMVar_ID_9369 Human_SNP_ID_5908954 A-to-I Human chr1 + 22029070 22029070 22029070 GGCACGCGCCACCATGCTCAGCTAATTTTTGTAATTTTAGTAGAGACGGGGTTTCTCCATGTTGG GGCACGCGCCACCATGCTCAGCTAATTTTTGTGATTTTAGTAGAGACGGGGTTTCTCCATGTTGG A G AL590556.3,LINC00339,CDC42 Ensembl:ENSG00000285959,Ensembl:ENSG00000218510,Ensembl:ENSG00000070831 lincRNA,lincRNA,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1303829738 Functional Loss SNV dbSNP153 33..33 33 - - - 9370 RMVar_ID_9370 Human_SNP_ID_5909122 A-to-I Human chr1 + 22029707 22029707 22029707 CGAGACCAGCCTGACCAACCTGGTGAAAGCCTATCTCTATGAAAAATACAAAATTTAGCTGGAGG CGAGACCAGCCTGACCAACCTGGTGAAAGCCTGTCTCTATGAAAAATACAAAATTTAGCTGGAGG A G AL590556.3,LINC00339,CDC42 Ensembl:ENSG00000285959,Ensembl:ENSG00000218510,Ensembl:ENSG00000070831 lincRNA,lincRNA,Protein coding intron,intron,intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1449562125 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9552907 9371 RMVar_ID_9371 Human_SNP_ID_5909125 A-to-I Human chr1 + 22029718 22029718 22029718 TGACCAACCTGGTGAAAGCCTATCTCTATGAAAAATACAAAATTTAGCTGGAGGTGGTGGCACGT TGACCAACCTGGTGAAAGCCTATCTCTATGAAGAATACAAAATTTAGCTGGAGGTGGTGGCACGT A G AL590556.3,LINC00339,CDC42 Ensembl:ENSG00000285959,Ensembl:ENSG00000218510,Ensembl:ENSG00000070831 lincRNA,lincRNA,Protein coding intron,intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs972735444 Functional Loss SNV dbSNP153 33..33 33 - - - 9372 RMVar_ID_9372 Human_SNP_ID_5909135 A-to-I Human chr1 + 22029747 22029747 22029747 GAAAAATACAAAATTTAGCTGGAGGTGGTGGCACGTGTCTGTAATCCCAGCCACTCAGGAGGCTG GAAAAATACAAAATTTAGCTGGAGGTGGTGGCGCGTGTCTGTAATCCCAGCCACTCAGGAGGCTG A G AL590556.3,LINC00339,CDC42 Ensembl:ENSG00000285959,Ensembl:ENSG00000218510,Ensembl:ENSG00000070831 lincRNA,lincRNA,Protein coding intron,intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1409287016 Functional Loss SNV dbSNP153 33..33 33 - - - 9373 RMVar_ID_9373 Human_SNP_ID_5909143 A-to-I Human chr1 + 22029767 22029767 22029767 GGAGGTGGTGGCACGTGTCTGTAATCCCAGCCACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAA GGAGGTGGTGGCACGTGTCTGTAATCCCAGCCGCTCAGGAGGCTGAGGCAGGAGAATTGCTTGAA A G AL590556.3,LINC00339,CDC42 Ensembl:ENSG00000285959,Ensembl:ENSG00000218510,Ensembl:ENSG00000070831 lincRNA,lincRNA,Protein coding intron,intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs985610944 Functional Loss SNV dbSNP153 33..33 33 - - - 9374 RMVar_ID_9374 Human_SNP_ID_5909144 A-to-I Human chr1 + 22029771 22029771 22029771 GTGGTGGCACGTGTCTGTAATCCCAGCCACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAACCTG GTGGTGGCACGTGTCTGTAATCCCAGCCACTCGGGAGGCTGAGGCAGGAGAATTGCTTGAACCTG A G AL590556.3,LINC00339,CDC42 Ensembl:ENSG00000285959,Ensembl:ENSG00000218510,Ensembl:ENSG00000070831 lincRNA,lincRNA,Protein coding intron,intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1287851468 Functional Loss SNV dbSNP153 33..33 33 - - - 9375 RMVar_ID_9375 Human_SNP_ID_5909153 A-to-I Human chr1 + 22029823 22029823 22029823 TTGCTTGAACCTGGGAGGCAGAGGTTGCGGTGAGCCGAGATCATGCCATTGCACTCCAGCCTGAA TTGCTTGAACCTGGGAGGCAGAGGTTGCGGTGGGCCGAGATCATGCCATTGCACTCCAGCCTGAA A G AL590556.3,LINC00339,CDC42 Ensembl:ENSG00000285959,Ensembl:ENSG00000218510,Ensembl:ENSG00000070831 lincRNA,lincRNA,Protein coding intron,intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs923689392 Functional Loss SNV dbSNP153 33..33 33 - - - 9376 RMVar_ID_9376 Human_SNP_ID_5917054 A-to-I Human chr1 + 22058662 22058662 22058662 GTGCCAGCATGCCTGGCTGATCTTGTATTTTTAGTAGAGATGGGGTTTCTCCATGTTGGGAGTTT GTGCCAGCATGCCTGGCTGATCTTGTATTTTTGGTAGAGATGGGGTTTCTCCATGTTGGGAGTTT A G CDC42 Ensembl:ENSG00000070831 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1443595919 Functional Loss SNV dbSNP153 33..33 33 - - - 9377 RMVar_ID_9377 Human_SNP_ID_5917453 A-to-I Human chr1 + 22060140 22060134 22060140 GAGGCAGGCAGATCACCTGAGGGCTGGAGTTCAAGACCAACCTGGCCAACATGGTGAAACCCCGT GAGGCAGGCAGATCACCTGAGGGCTGG______AGACCAACCTGGCCAACATGGTGAAACCCCGT GAGTTCA G CDC42-IT1,CDC42 Ensembl:ENSG00000230068,Ensembl:ENSG00000070831 lincRNA,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1478019012 Functional Loss DEL dbSNP153 28..33 33 - - - 9378 RMVar_ID_9378 Human_SNP_ID_5917465 A-to-I Human chr1 + 22060180 22060180 22060180 CCTGGCCAACATGGTGAAACCCCGTCTTTACTAAAAATACAAAAATTAGCCATGGTGGCATGCAC CCTGGCCAACATGGTGAAACCCCGTCTTTACTGAAAATACAAAAATTAGCCATGGTGGCATGCAC A G CDC42-IT1,CDC42 Ensembl:ENSG00000230068,Ensembl:ENSG00000070831 lincRNA,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs562776517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8243587 9379 RMVar_ID_9379 Human_SNP_ID_5917478 A-to-I Human chr1 + 22060207 22060207 22060207 TTACTAAAAATACAAAAATTAGCCATGGTGGCATGCACCTGTAATCCCAGCTACTTGAGAGGCTG TTACTAAAAATACAAAAATTAGCCATGGTGGCGTGCACCTGTAATCCCAGCTACTTGAGAGGCTG A G CDC42-IT1,CDC42 Ensembl:ENSG00000230068,Ensembl:ENSG00000070831 lincRNA,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs988524184 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8243587 9380 RMVar_ID_9380 Human_SNP_ID_5917479 A-to-I Human chr1 + 22060211 22060211 22060211 TAAAAATACAAAAATTAGCCATGGTGGCATGCACCTGTAATCCCAGCTACTTGAGAGGCTGAGGC TAAAAATACAAAAATTAGCCATGGTGGCATGCGCCTGTAATCCCAGCTACTTGAGAGGCTGAGGC A G CDC42-IT1,CDC42 Ensembl:ENSG00000230068,Ensembl:ENSG00000070831 lincRNA,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs949546729 Functional Loss SNV dbSNP153 33..33 33 - - - 9381 RMVar_ID_9381 Human_SNP_ID_5917495 A-to-I Human chr1 + 22060270 22060270 22060270 TGAGGCACGAGAATCGCTTGAACCTGGGATGCAGAGGCTGCAGTGAGCGGGGATGCACCACTGTT TGAGGCACGAGAATCGCTTGAACCTGGGATGCGGAGGCTGCAGTGAGCGGGGATGCACCACTGTT A G CDC42-IT1,CDC42 Ensembl:ENSG00000230068,Ensembl:ENSG00000070831 lincRNA,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1329063268 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5893768,Human_RBP_ID_17557033 9382 RMVar_ID_9382 Human_SNP_ID_5917929 A-to-I Human chr1 + 22061709 22061709 22061709 GGGATTACAGGTGCCCGCCACCATGCCCGGCTAATTTTTGTATTTTTAGTGGAGATGTTGGCCAT GGGATTACAGGTGCCCGCCACCATGCCCGGCTGATTTTTGTATTTTTAGTGGAGATGTTGGCCAT A G CDC42-IT1,CDC42 Ensembl:ENSG00000230068,Ensembl:ENSG00000070831 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1158049417 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9489071 9383 RMVar_ID_9383 Human_SNP_ID_5918524 A-to-I Human chr1 + 22063956 22063956 22063956 TGACCAGGCTGGTCTGGAACTCCTGACCTCTTATGATCTTCCTGCCTTGGCCTCCCAAAGTGCTG TGACCAGGCTGGTCTGGAACTCCTGACCTCTTGTGATCTTCCTGCCTTGGCCTCCCAAAGTGCTG A G CDC42-IT1,CDC42 Ensembl:ENSG00000230068,Ensembl:ENSG00000070831 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1379872803 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8243229 9384 RMVar_ID_9384 Human_SNP_ID_5919074 A-to-I Human chr1 + 22065836 22065836 22065836 CAGGCTGGAGTGCAGTGGCATGATCTCAGCTCACTGCAACCTCCTCCCGGGTTCAAGCGATTCTC CAGGCTGGAGTGCAGTGGCATGATCTCAGCTCGCTGCAACCTCCTCCCGGGTTCAAGCGATTCTC A G CDC42 Ensembl:ENSG00000070831 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037688620 Functional Loss SNV dbSNP153 33..33 33 - - - 9385 RMVar_ID_9385 Human_SNP_ID_5919364 A-to-I Human chr1 + 22066959 22066959 22066959 GTGGCACATGCCTGTAATTCCAGCTACTCAGGAAGTTGAGGCTGGAAAATCGCTTGAACCTGGGA GTGGCACATGCCTGTAATTCCAGCTACTCAGGGAGTTGAGGCTGGAAAATCGCTTGAACCTGGGA A G CDC42 Ensembl:ENSG00000070831 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1457818519 Functional Loss SNV dbSNP153 33..33 33 - - - 9386 RMVar_ID_9386 Human_SNP_ID_5921166 A-to-I Human chr1 + 22073350 22073350 22073350 CCTGAGGTCAGGATTTTGAGACCAGCCTGGCCAATGTGGCGAAACCCCGTCTCTACTAAAAAAAT CCTGAGGTCAGGATTTTGAGACCAGCCTGGCCGATGTGGCGAAACCCCGTCTCTACTAAAAAAAT A G CDC42 Ensembl:ENSG00000070831 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1239211374 Functional Loss SNV dbSNP153 33..33 33 - - - 9387 RMVar_ID_9387 Human_SNP_ID_5921292 A-to-I Human chr1 + 22073819 22073818 22073819 GGGACTACAGGTGTGTGCCACTTCACCCAGCTAATTTTTTTTTTTGTAGAGATGGGGTCTCACTC GGGACTACAGGTGTGTGCCACTTCACCCAGCT_ATTTTTTTTTTTGTAGAGATGGGGTCTCACTC TA T CDC42 Ensembl:ENSG00000070831 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1480344330 Functional Loss DEL dbSNP153 33..33 33 - - - 9388 RMVar_ID_9388 Human_SNP_ID_5923355 A-to-I Human chr1 + 22082034 22082034 22082034 GAACAGTGTAGTAGATGAAGTAGAGTGAGACTAGAGTGCATCATACAAGCTCCAAATTGAACTAA GAACAGTGTAGTAGATGAAGTAGAGTGAGACTGGAGTGCATCATACAAGCTCCAAATTGAACTAA A G CDC42 Ensembl:ENSG00000070831 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2056975 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_652,GWAS_ID_653,GWAS_ID_654,GWAS_ID_655,GWAS_ID_656,GWAS_ID_657,GWAS_ID_658,GWAS_ID_659,GWAS_ID_660,GWAS_ID_661,GWAS_ID_662,GWAS_ID_663,GWAS_ID_664,GWAS_ID_665,GWAS_ID_666,GWAS_ID_667,GWAS_ID_668,GWAS_ID_669,GWAS_ID_670,GWAS_ID_671,GWAS_ID_672,GWAS_ID_673,GWAS_ID_674,GWAS_ID_675,GWAS_ID_676,GWAS_ID_677,GWAS_ID_678,GWAS_ID_679,GWAS_ID_680,GWAS_ID_681,GWAS_ID_682,GWAS_ID_683,GWAS_ID_684 RMVar_hsa_circ_97695,RMVar_hsa_circ_103628,RMVar_hsa_circ_342544,RMVar_hsa_circ_130355,RMVar_hsa_circ_378086,RMVar_hsa_circ_345538,RMVar_hsa_circ_276873,RMVar_hsa_circ_100439,RMVar_hsa_circ_104993,RMVar_hsa_circ_130356,RMVar_hsa_circ_130357,RMVar_hsa_circ_130358,RMVar_hsa_circ_127635,RMVar_hsa_circ_130359,RMVar_hsa_circ_130360,RMVar_hsa_circ_130362 9389 RMVar_ID_9389 Human_SNP_ID_5923356 A-to-I Human chr1 + 22082034 22082034 22082034 GAACAGTGTAGTAGATGAAGTAGAGTGAGACTAGAGTGCATCATACAAGCTCCAAATTGAACTAA GAACAGTGTAGTAGATGAAGTAGAGTGAGACTTGAGTGCATCATACAAGCTCCAAATTGAACTAA A T CDC42 Ensembl:ENSG00000070831 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2056975 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_652,GWAS_ID_653,GWAS_ID_654,GWAS_ID_655,GWAS_ID_656,GWAS_ID_657,GWAS_ID_658,GWAS_ID_659,GWAS_ID_660,GWAS_ID_661,GWAS_ID_662,GWAS_ID_663,GWAS_ID_664,GWAS_ID_665,GWAS_ID_666,GWAS_ID_667,GWAS_ID_668,GWAS_ID_669,GWAS_ID_670,GWAS_ID_671,GWAS_ID_672,GWAS_ID_673,GWAS_ID_674,GWAS_ID_675,GWAS_ID_676,GWAS_ID_677,GWAS_ID_678,GWAS_ID_679,GWAS_ID_680,GWAS_ID_681,GWAS_ID_682,GWAS_ID_683,GWAS_ID_684 RMVar_hsa_circ_97695,RMVar_hsa_circ_103628,RMVar_hsa_circ_342544,RMVar_hsa_circ_130355,RMVar_hsa_circ_378086,RMVar_hsa_circ_345538,RMVar_hsa_circ_276873,RMVar_hsa_circ_100439,RMVar_hsa_circ_104993,RMVar_hsa_circ_130356,RMVar_hsa_circ_130357,RMVar_hsa_circ_130358,RMVar_hsa_circ_127635,RMVar_hsa_circ_130359,RMVar_hsa_circ_130360,RMVar_hsa_circ_130362 9390 RMVar_ID_9390 Human_SNP_ID_5924416 A-to-I Human chr1 + 22085871 22085871 22085871 CTGTGATTGTTTCTTTACCATATCTGAGATGGAGTCTCACTCTGTCACCCAGACTGGAGTACAGT CTGTGATTGTTTCTTTACCATATCTGAGATGGCGTCTCACTCTGTCACCCAGACTGGAGTACAGT A C CDC42 Ensembl:ENSG00000070831 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1057089161 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10790269 RMVar_hsa_circ_97695,RMVar_hsa_circ_103628,RMVar_hsa_circ_342544,RMVar_hsa_circ_130355,RMVar_hsa_circ_378086,RMVar_hsa_circ_345538,RMVar_hsa_circ_276873,RMVar_hsa_circ_100439,RMVar_hsa_circ_104993,RMVar_hsa_circ_130356,RMVar_hsa_circ_130357,RMVar_hsa_circ_130358,RMVar_hsa_circ_127635,RMVar_hsa_circ_130359,RMVar_hsa_circ_130360,RMVar_hsa_circ_130362 9391 RMVar_ID_9391 Human_SNP_ID_5930492 A-to-I Human chr1 + 22110562 22110562 22110562 CTCCTGCCTCGGCCTCCCAAAGTGCTGGGACTACAGGCATGAGCCACCGTGCCTTGAACTTGAAC CTCCTGCCTCGGCCTCCCAAAGTGCTGGGACTGCAGGCATGAGCCACCGTGCCTTGAACTTGAAC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904336527 Functional Loss SNV dbSNP153 33..33 33 - - - 9392 RMVar_ID_9392 Human_SNP_ID_5951773 A-to-I Human chr1 + 22195551 22195551 22195551 TTCCTGCCTCGGCCTCCCAAGTAGTTGGGATTACAGGTGCTCGCCACCACGCCAGGCAATTTTTT TTCCTGCCTCGGCCTCCCAAGTAGTTGGGATTGCAGGTGCTCGCCACCACGCCAGGCAATTTTTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs999287494 Functional Loss SNV dbSNP153 33..33 33 - - - 9393 RMVar_ID_9393 Human_SNP_ID_6155356 A-to-I Human chr1 - 23012261 23012253 23012261 TGGCTCACTGCAGCCTCGACCTCCCTGGGATCAGGTGATCCTTCCACCTCAGCCTCCCAAGTAGC TGGCTCACTGCAGCCTCGACCTCCCTGGGATC________CTTCCACCTCAGCCTCCCAAGTAGC GGATCACCT G TEX46 Ensembl:ENSG00000227868 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1200731214 Functional Loss DEL dbSNP153 33..40 33 - - - 9394 RMVar_ID_9394 Human_SNP_ID_6155357 A-to-I Human chr1 - 23012261 23012261 23012261 TGGCTCACTGCAGCCTCGACCTCCCTGGGATCAGGTGATCCTTCCACCTCAGCCTCCCAAGTAGC TGGCTCACTGCAGCCTCGACCTCCCTGGGATCCGGTGATCCTTCCACCTCAGCCTCCCAAGTAGC T G TEX46 Ensembl:ENSG00000227868 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1443842619 Functional Loss SNV dbSNP153 33..33 33 - - - 9395 RMVar_ID_9395 Human_SNP_ID_6161184 A-to-I Human chr1 + 23035411 23035411 23035411 TTTAGTAGAGATGAGGTTTCTCCGCGTTGGCCAGGCTGATCTCGAACTCCTGACCTCAGGTGATC TTTAGTAGAGATGAGGTTTCTCCGCGTTGGCCGGGCTGATCTCGAACTCCTGACCTCAGGTGATC A G KDM1A Ensembl:ENSG00000004487 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1471942136 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10843732 RMVar_hsa_circ_30637,RMVar_hsa_circ_130376,RMVar_hsa_circ_84363,RMVar_hsa_circ_122955,RMVar_hsa_circ_130377,RMVar_hsa_circ_272956,RMVar_hsa_circ_290300,RMVar_hsa_circ_306641,RMVar_hsa_circ_130378,RMVar_hsa_circ_343676,RMVar_hsa_circ_278303,RMVar_hsa_circ_116350,RMVar_hsa_circ_272701,RMVar_hsa_circ_92732,RMVar_hsa_circ_130381,RMVar_hsa_circ_130383,RMVar_hsa_circ_130385,RMVar_hsa_circ_130386,RMVar_hsa_circ_130384,RMVar_hsa_circ_130382,RMVar_hsa_circ_130387,RMVar_hsa_circ_130379,RMVar_hsa_circ_130380,RMVar_hsa_circ_130388 9396 RMVar_ID_9396 Human_SNP_ID_6186076 A-to-I Human chr1 - 23139874 23139874 23139874 ATGAGCACAGCTTACAGCAGTCTCAGCCTCCCAGGCTCAAGTGATCCTCCCACCTCAGCCTCCTA ATGAGCACAGCTTACAGCAGTCTCAGCCTCCCGGGCTCAAGTGATCCTCCCACCTCAGCCTCCTA T C LUZP1 Ensembl:ENSG00000169641 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1488519766 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92586,RMVar_hsa_circ_130445,RMVar_hsa_circ_289557 9397 RMVar_ID_9397 Human_SNP_ID_6186077 A-to-I Human chr1 - 23139874 23139874 23139874 ATGAGCACAGCTTACAGCAGTCTCAGCCTCCCAGGCTCAAGTGATCCTCCCACCTCAGCCTCCTA ATGAGCACAGCTTACAGCAGTCTCAGCCTCCCCGGCTCAAGTGATCCTCCCACCTCAGCCTCCTA T G LUZP1 Ensembl:ENSG00000169641 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1488519766 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92586,RMVar_hsa_circ_130445,RMVar_hsa_circ_289557 9398 RMVar_ID_9398 Human_SNP_ID_6189487 A-to-I Human chr1 - 23154349 23154349 23154349 AATTTTTTTTTTGTAGAGATGGGGGTCTGGCTATGTTGCCCAGGCTGGTGTTGAACTCTTGGCCT AATTTTTTTTTTGTAGAGATGGGGGTCTGGCTGTGTTGCCCAGGCTGGTGTTGAACTCTTGGCCT T C LUZP1 Ensembl:ENSG00000169641 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1162330577 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24657751 RMVar_hsa_circ_92586,RMVar_hsa_circ_130445,RMVar_hsa_circ_289557 9399 RMVar_ID_9399 Human_SNP_ID_6189528 A-to-I Human chr1 - 23154533 23154531 23154533 GTCTCAAAAAAAAAAGAAAAGAAAAAGAAGACAGGGTCTTACTCTGTTCCCTAGGCTGGAATGCA GTCTCAAAAAAAAAAGAAAAGAAAAAGAAGAC__GGTCTTACTCTGTTCCCTAGGCTGGAATGCA CCT C LUZP1 Ensembl:ENSG00000169641 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1477557068 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_92586,RMVar_hsa_circ_130445,RMVar_hsa_circ_289557 9400 RMVar_ID_9400 Human_SNP_ID_6223268 A-to-I Human chr1 - 23293424 23293424 23293424 GGGACTATAGGTGTGCACCACCACACACGGCTAATTTTTGCGTTTTTAATAGAGATGGAGTTTCA GGGACTATAGGTGTGCACCACCACACACGGCTGATTTTTGCGTTTTTAATAGAGATGGAGTTTCA T C LINC01355 RNACentral:URS00008B2DF2 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs957160543 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24661655 9401 RMVar_ID_9401 Human_SNP_ID_6225374 A-to-I Human chr1 - 23300926 23300926 23300926 GGGAGGCAGAGGTTGCACTGAGGCGAGATCGCACCACTGCCCTCCAGCCTGGGCGAGAGAGTGAG GGGAGGCAGAGGTTGCACTGAGGCGAGATCGCGCCACTGCCCTCCAGCCTGGGCGAGAGAGTGAG T C LINC01355 RNACentral:URS00008B2DF2 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1353019309 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23303291 9402 RMVar_ID_9402 Human_SNP_ID_6225385 A-to-I Human chr1 - 23300951 23300951 23300951 TGAGACAGGAGAATCACTTAAAACCGGGAGGCAGAGGTTGCACTGAGGCGAGATCGCACCACTGC TGAGACAGGAGAATCACTTAAAACCGGGAGGCGGAGGTTGCACTGAGGCGAGATCGCACCACTGC T C LINC01355 RNACentral:URS00008B2DF2 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs541628313 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24661869 9403 RMVar_ID_9403 Human_SNP_ID_6225765 A-to-I Human chr1 - 23302572 23302572 23302572 ACTTTTCTTTTCTTTTCTTTTCTTTTTGAGACAGAGTCTCCCTGTGTCGCCCAGGCTGGAGTGCA ACTTTTCTTTTCTTTTCTTTTCTTTTTGAGACGGAGTCTCCCTGTGTCGCCCAGGCTGGAGTGCA T C LINC01355 RNACentral:URS00008B2DF2 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1303389104 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5907220 9404 RMVar_ID_9404 Human_SNP_ID_6225924 A-to-I Human chr1 - 23303146 23303146 23303146 TTGAGCCCCGGAGTTCAAGATCAGCCTGGGCAACATAGGGAGACCCCATCTCTACAAAAAATCAG TTGAGCCCCGGAGTTCAAGATCAGCCTGGGCACCATAGGGAGACCCCATCTCTACAAAAAATCAG T G LINC01355 RNACentral:URS00008B2DF2 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs897762302 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5785988 9405 RMVar_ID_9405 Human_SNP_ID_6231800 A-to-I Human chr1 - 23327516 23327516 23327516 CTGACTAATTTTTTGTATTTTTAGTTACAGACAGGGTTTCACCATATTGGCCAGGCTGGTCTCAA CTGACTAATTTTTTGTATTTTTAGTTACAGACGGGGTTTCACCATATTGGCCAGGCTGGTCTCAA T C HNRNPR Ensembl:ENSG00000125944 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1257326851 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_557,RMVar_hsa_circ_67146,RMVar_hsa_circ_55437,RMVar_hsa_circ_356207,RMVar_hsa_circ_305724,RMVar_hsa_circ_292881,RMVar_hsa_circ_320103,RMVar_hsa_circ_371291,RMVar_hsa_circ_130450 9406 RMVar_ID_9406 Human_SNP_ID_6231814 A-to-I Human chr1 - 23327578 23327578 23327578 TCAAGTGATTCTTCTGCCTAAGCCTCCAGAGTAGCTGGGATTACAGGCTTGTGCCACCATGCCTG TCAAGTGATTCTTCTGCCTAAGCCTCCAGAGTGGCTGGGATTACAGGCTTGTGCCACCATGCCTG T C HNRNPR Ensembl:ENSG00000125944 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1329029325 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_557,RMVar_hsa_circ_67146,RMVar_hsa_circ_55437,RMVar_hsa_circ_356207,RMVar_hsa_circ_305724,RMVar_hsa_circ_292881,RMVar_hsa_circ_320103,RMVar_hsa_circ_371291,RMVar_hsa_circ_130450 9407 RMVar_ID_9407 Human_SNP_ID_6231827 A-to-I Human chr1 - 23327627 23327627 23327627 GGAGTGCAGTGGCGTGATCTCCGCTCACTGCAACCTCCACCTTCCTGGTTCAAGTGATTCTTCTG GGAGTGCAGTGGCGTGATCTCCGCTCACTGCAGCCTCCACCTTCCTGGTTCAAGTGATTCTTCTG T C HNRNPR Ensembl:ENSG00000125944 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1332438055 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_557,RMVar_hsa_circ_67146,RMVar_hsa_circ_55437,RMVar_hsa_circ_356207,RMVar_hsa_circ_305724,RMVar_hsa_circ_292881,RMVar_hsa_circ_320103,RMVar_hsa_circ_371291,RMVar_hsa_circ_130450 9408 RMVar_ID_9408 Human_SNP_ID_6232207 A-to-I Human chr1 - 23329069 23329069 23329069 TTGCCCAGGCTGGAGTACAGTGGCACAATCGTAGCTCACTGCAACCTCAAACTCCTGGGTTTAGG TTGCCCAGGCTGGAGTACAGTGGCACAATCGTGGCTCACTGCAACCTCAAACTCCTGGGTTTAGG T C HNRNPR Ensembl:ENSG00000125944 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs955754143 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_557,RMVar_hsa_circ_67146,RMVar_hsa_circ_55437,RMVar_hsa_circ_356207,RMVar_hsa_circ_305724,RMVar_hsa_circ_292881,RMVar_hsa_circ_320103,RMVar_hsa_circ_371291,RMVar_hsa_circ_130450 9409 RMVar_ID_9409 Human_SNP_ID_6232355 A-to-I Human chr1 - 23329801 23329798 23329801 CATAAGGAGACCCTGTCTCTATAAAAAATAAAAAATTAGCCAGGCATGGTGGCATGCGCACAGCT CATAAGGAGACCCTGTCTCTATAAAAAATAAA___TTAGCCAGGCATGGTGGCATGCGCACAGCT ATTT A HNRNPR Ensembl:ENSG00000125944 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965810791 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_557,RMVar_hsa_circ_67146,RMVar_hsa_circ_55437,RMVar_hsa_circ_356207,RMVar_hsa_circ_305724,RMVar_hsa_circ_292881,RMVar_hsa_circ_320103,RMVar_hsa_circ_371291,RMVar_hsa_circ_130450 9410 RMVar_ID_9410 Human_SNP_ID_6232541 A-to-I Human chr1 - 23330496 23330496 23330496 GAGTCTCACTCTGTCGCCCAGGCTGGAGTGTAATGGCACGATCTCGGCTCACTGCAACCTCCGCC GAGTCTCACTCTGTCGCCCAGGCTGGAGTGTAGTGGCACGATCTCGGCTCACTGCAACCTCCGCC T C HNRNPR Ensembl:ENSG00000125944 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs370494851 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10859681 RMVar_hsa_circ_557,RMVar_hsa_circ_67146,RMVar_hsa_circ_55437,RMVar_hsa_circ_356207,RMVar_hsa_circ_305724,RMVar_hsa_circ_292881,RMVar_hsa_circ_320103,RMVar_hsa_circ_371291,RMVar_hsa_circ_130450 9411 RMVar_ID_9411 Human_SNP_ID_6233607 A-to-I Human chr1 - 23333944 23333944 23333944 ATGCCACTGCACTCCAGCCTGGGCAACAGAGCAAGACTCCATCTCAAAAAAAAAGAAGAAAAGAC ATGCCACTGCACTCCAGCCTGGGCAACAGAGCGAGACTCCATCTCAAAAAAAAAGAAGAAAAGAC T C HNRNPR Ensembl:ENSG00000125944 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs948817899 Functional Loss SNV dbSNP153 33..33 33 - - - 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_130452 9412 RMVar_ID_9412 Human_SNP_ID_6246460 A-to-I Human chr1 - 23381148 23381148 23381148 AACTCTGGGAGGCTGAGGTGGGAGAATCGCTTAACCCCAGAAGTTTGAGTCCAGCCCAGGCAACA AACTCTGGGAGGCTGAGGTGGGAGAATCGCTTGACCCCAGAAGTTTGAGTCCAGCCCAGGCAACA T C TCEA3 Ensembl:ENSG00000204219 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs3192564 Functional Loss SNV dbSNP153 33..33 33 - - - 9413 RMVar_ID_9413 Human_SNP_ID_6253956 A-to-I Human chr1 + 23410839 23410839 23410839 AAAGAAAAGAAAGAAAATAGAAACCATGTTTCAAAGACCTGTATTACAGGTACTTCATCAGTTTG AAAGAAAAGAAAGAAAATAGAAACCATGTTTCGAAGACCTGTATTACAGGTACTTCATCAGTTTG A G AL357134.1 Ensembl:ENSG00000232482 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1230860726 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4092008,Human_RBP_ID_8241156,Human_RBP_ID_18524374,Human_RBP_ID_22783143 9414 RMVar_ID_9414 Human_SNP_ID_6253961 A-to-I Human chr1 + 23410863 23410863 23410863 CATGTTTCAAAGACCTGTATTACAGGTACTTCATCAGTTTGTAAGGCATGAGTCCAAAACAGCTA CATGTTTCAAAGACCTGTATTACAGGTACTTCGTCAGTTTGTAAGGCATGAGTCCAAAACAGCTA A G AL357134.1 Ensembl:ENSG00000232482 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1229826786 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18524374 9415 RMVar_ID_9415 Human_SNP_ID_6253968 A-to-I Human chr1 + 23410886 23410886 23410886 AGGTACTTCATCAGTTTGTAAGGCATGAGTCCAAAACAGCTAGCAGTTTGGTTCTTGAAAGATCC AGGTACTTCATCAGTTTGTAAGGCATGAGTCCGAAACAGCTAGCAGTTTGGTTCTTGAAAGATCC A G AL357134.1 Ensembl:ENSG00000232482 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1187391819 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26377385 9416 RMVar_ID_9416 Human_SNP_ID_6267861 A-to-I Human chr1 - 23466996 23466996 23466996 AGGTGCAGTGGCGCATGCCTGTAATCCCAGCTACTCTGGAGGCTGAGGCAGGATAATTGCTTGAA AGGTGCAGTGGCGCATGCCTGTAATCCCAGCTGCTCTGGAGGCTGAGGCAGGATAATTGCTTGAA T C ASAP3 Ensembl:ENSG00000088280 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1251789172 Functional Loss SNV dbSNP153 33..33 33 - - - 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 9417 RMVar_ID_9417 Human_SNP_ID_6279536 A-to-I Human chr1 - 23511981 23511981 23511981 GTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCTGCCTGCCTCGCCCTCCCAAAGTGC GTTGGCCAGGCTGGTCTCGAACTCCTGACCTCGGGTGATCTGCCTGCCTCGCCCTCCCAAAGTGC T C E2F2 Ensembl:ENSG00000007968 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1216282980 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110735,RMVar_hsa_circ_130473 9418 RMVar_ID_9418 Human_SNP_ID_6280082 A-to-I Human chr1 - 23513889 23513889 23513889 GAACTCCTGATCTCAGGTGATCCACCCACCTCAGCTTCCCAAAGTGCTGGGATTACAGGTGTGAG GAACTCCTGATCTCAGGTGATCCACCCACCTCGGCTTCCCAAAGTGCTGGGATTACAGGTGTGAG T C E2F2 Ensembl:ENSG00000007968 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs576645159 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110735,RMVar_hsa_circ_130473 9419 RMVar_ID_9419 Human_SNP_ID_6280084 A-to-I Human chr1 - 23513907 23513907 23513907 GTTGGCCAGGCTGGTCTCGAACTCCTGATCTCAGGTGATCCACCCACCTCAGCTTCCCAAAGTGC GTTGGCCAGGCTGGTCTCGAACTCCTGATCTCGGGTGATCCACCCACCTCAGCTTCCCAAAGTGC T C E2F2 Ensembl:ENSG00000007968 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs868858954 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110735,RMVar_hsa_circ_130473 9420 RMVar_ID_9420 Human_SNP_ID_6280571 A-to-I Human chr1 - 23515901 23515901 23515901 GACCAGGAGTTCAAGAGCAGCCCGGGCAACATAGGGATACCCTGTCTCTATAAAAAAATTTACAA GACCAGGAGTTCAAGAGCAGCCCGGGCAACATGGGGATACCCTGTCTCTATAAAAAAATTTACAA T C E2F2 Ensembl:ENSG00000007968 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1249427429 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110735,RMVar_hsa_circ_130473 9421 RMVar_ID_9421 Human_SNP_ID_6280574 A-to-I Human chr1 - 23515905 23515905 23515905 TTGAGACCAGGAGTTCAAGAGCAGCCCGGGCAACATAGGGATACCCTGTCTCTATAAAAAAATTT TTGAGACCAGGAGTTCAAGAGCAGCCCGGGCAGCATAGGGATACCCTGTCTCTATAAAAAAATTT T C E2F2 Ensembl:ENSG00000007968 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1416516534 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110735,RMVar_hsa_circ_130473 9422 RMVar_ID_9422 Human_SNP_ID_6280615 A-to-I Human chr1 - 23516088 23516088 23516088 CCAGCCCATCCACTTACCAGCTATGTGACCTTAGACAAGTTACTTAACCTCTCTTGGCCTCAATT CCAGCCCATCCACTTACCAGCTATGTGACCTTGGACAAGTTACTTAACCTCTCTTGGCCTCAATT T C E2F2 Ensembl:ENSG00000007968 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs987731520 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110735,RMVar_hsa_circ_130473 9423 RMVar_ID_9423 Human_SNP_ID_6292318 A-to-I Human chr1 - 23558349 23558349 23558349 CCGGGAACCTCTCCTGCCGGAAGCCGGACGGCAGGGATGGGCCCCAACTTCGCCCTGCCCACTTG CCGGGAACCTCTCCTGCCGGAAGCCGGACGGCGGGGATGGGCCCCAACTTCGCCCTGCCCACTTG T C ID3 Ensembl:ENSG00000117318 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs112269197 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_220879,Human_RBP_ID_347766,Human_RBP_ID_17647401,Human_RBP_ID_26377412,Human_RBP_ID_27178958,Human_RBP_ID_27395946 Human_Splice_Rec_30240,Human_Splice_Rec_30242 Human_miRNA_ID_443594 RMVar_hsa_circ_130476,RMVar_hsa_circ_100881,RMVar_hsa_circ_124280,RMVar_hsa_circ_130477 9424 RMVar_ID_9424 Human_SNP_ID_6335122 A-to-I Human chr1 + 23721599 23721599 23721599 GAGTTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACGATGTCTCTACTAAAAATACAAA GAGTTCAGGAGTTCGAGACCAGCCTGGCCAACGTGGTGAAACGATGTCTCTACTAAAAATACAAA A G lnc-BBS5-6 RNACentral:URS0000E2127A lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1160601561 Functional Loss SNV dbSNP153 33..33 33 - - - 9425 RMVar_ID_9425 Human_SNP_ID_6339177 A-to-I Human chr1 + 23737936 23737936 23737936 ACTGATCTCGAACTACTGACCCCAGGTGATCCACCCGCCTCAGCCTTCCAAAGTGCTGGGATTAC ACTGATCTCGAACTACTGACCCCAGGTGATCCCCCCGCCTCAGCCTTCCAAAGTGCTGGGATTAC A C lnc-BBS5-6 RNACentral:URS0000E2127A lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs918900754 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10866845 9426 RMVar_ID_9426 Human_SNP_ID_6344426 A-to-I Human chr1 + 23757918 23757918 23757918 GAAAAATTAGCCCACCATGGTGGCATGTGCCTATAATCTCAGGTACTCGGGTGGCTGAGACAGGA GAAAAATTAGCCCACCATGGTGGCATGTGCCTGTAATCTCAGGTACTCGGGTGGCTGAGACAGGA A G ELOA Ensembl:ENSG00000011007 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs377278717 Functional Loss SNV dbSNP153 33..33 33 - - - 9427 RMVar_ID_9427 Human_SNP_ID_6345729 A-to-I Human chr1 - 23762596 23762596 23762596 CAGCTCACTGTAGCCTCGACCTCCCAAGCTCAAGTGATCCTCCCACCTCAGCCTTTCACATAGCT CAGCTCACTGTAGCCTCGACCTCCCAAGCTCAGGTGATCCTCCCACCTCAGCCTTTCACATAGCT T C ELOA-AS1 Ensembl:ENSG00000236810 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042158156 Functional Loss SNV dbSNP153 33..33 33 - - - 9428 RMVar_ID_9428 Human_SNP_ID_6346503 A-to-I Human chr1 - 23765335 23765335 23765335 ACTAGGGAGGCTGAAGCAGGAGAATCACATGAACCCGGGAGGCAGAGGTTGCAGTGAGCCGAGAG ACTAGGGAGGCTGAAGCAGGAGAATCACATGAGCCCGGGAGGCAGAGGTTGCAGTGAGCCGAGAG T C ELOA-AS1 Ensembl:ENSG00000236810 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1379717902 Functional Loss SNV dbSNP153 33..33 33 - - - 9429 RMVar_ID_9429 Human_SNP_ID_6346527 A-to-I Human chr1 - 23765429 23765429 23765429 GAGGTCAGGAGTTCAAGACCAGCCTAGCCAACATGGTGAAACCCATCTCTACTAAAAATACAAAA GAGGTCAGGAGTTCAAGACCAGCCTAGCCAACGTGGTGAAACCCATCTCTACTAAAAATACAAAA T C ELOA-AS1 Ensembl:ENSG00000236810 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs574010317 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5245695 9430 RMVar_ID_9430 Human_SNP_ID_6346786 A-to-I Human chr1 - 23766498 23766498 23766498 CCTCAACCTCCCCGAGTTCAAGCAATCCTCCCACCTCAGCCTCCTGAGTAGCTAGAACTACAGGT CCTCAACCTCCCCGAGTTCAAGCAATCCTCCCGCCTCAGCCTCCTGAGTAGCTAGAACTACAGGT T C ELOA-AS1 Ensembl:ENSG00000236810 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs753154392 Functional Loss SNV dbSNP153 33..33 33 - - - 9431 RMVar_ID_9431 Human_SNP_ID_6347802 A-to-I Human chr1 - 23770066 23770066 23770066 TGGTCTTGATCTCCTGACCTCGTGATCCGCCCACCTTGGCCTCCCAAAGTGCTGGGATTACAGGC TGGTCTTGATCTCCTGACCTCGTGATCCGCCCTCCTTGGCCTCCCAAAGTGCTGGGATTACAGGC T A ELOA-AS1 Ensembl:ENSG00000236810 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1249120834 Functional Loss SNV dbSNP153 33..33 33 - - - 9432 RMVar_ID_9432 Human_SNP_ID_6347803 A-to-I Human chr1 - 23770066 23770066 23770066 TGGTCTTGATCTCCTGACCTCGTGATCCGCCCACCTTGGCCTCCCAAAGTGCTGGGATTACAGGC TGGTCTTGATCTCCTGACCTCGTGATCCGCCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGC T C ELOA-AS1 Ensembl:ENSG00000236810 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1249120834 Functional Loss SNV dbSNP153 33..33 33 - - - 9433 RMVar_ID_9433 Human_SNP_ID_6349253 A-to-I Human chr1 - 23775998 23775998 23775998 ATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCAGGAGGCAGAGGTTGCAGTG ATCCCAGCTACTCGGGAGGCTGAGGCAGGAGATTCGCTTGAACCCAGGAGGCAGAGGTTGCAGTG T A ELOA-AS1 Ensembl:ENSG00000236810 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs925534347 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_103827 9434 RMVar_ID_9434 Human_SNP_ID_6351166 A-to-I Human chr1 + 23782696 23782696 23782696 TGATCATAGCTCACTGCAGCCTCGACCTCCTCAGTTCAAGCAATCCTCCCACCGCAGCCTCCCAA TGATCATAGCTCACTGCAGCCTCGACCTCCTCCGTTCAAGCAATCCTCCCACCGCAGCCTCCCAA A C PITHD1 Ensembl:ENSG00000057757 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264804908 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106493,RMVar_hsa_circ_88041,RMVar_hsa_circ_130497,RMVar_hsa_circ_336347,RMVar_hsa_circ_130498 9435 RMVar_ID_9435 Human_SNP_ID_6351560 A-to-I Human chr1 + 23783470 23783470 23783470 TGTGTGTGTGTGTGTGTATTTTTTGTTTTTTTAAGACGGCGTTCTGCTCTGTTGCCTAGGCTTGA TGTGTGTGTGTGTGTGTATTTTTTGTTTTTTTTAGACGGCGTTCTGCTCTGTTGCCTAGGCTTGA A T PITHD1 Ensembl:ENSG00000057757 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1451079425 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3305387,Human_RBP_ID_10867810 RMVar_hsa_circ_106493,RMVar_hsa_circ_88041,RMVar_hsa_circ_130497,RMVar_hsa_circ_336347,RMVar_hsa_circ_130498 9436 RMVar_ID_9436 Human_SNP_ID_6362377 A-to-I Human chr1 - 23822917 23822917 23822917 CCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCACGCTTGGCCTGAAGCAGG CCCACCTCGGCCTCCCAAAGTGCTGGGATTACGGGCGTGAGCCACCACGCTTGGCCTGAAGCAGG T C HMGCL Ensembl:ENSG00000117305 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1045371972 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55703,RMVar_hsa_circ_360771 9437 RMVar_ID_9437 Human_SNP_ID_6362404 A-to-I Human chr1 - 23823048 23823048 23823048 CCTCAGCCTCCCGAGTAGCTGGGATTGCAGGCACCTGCTGCCATGCCTAGCTAATTTATGTGTTT CCTCAGCCTCCCGAGTAGCTGGGATTGCAGGCCCCTGCTGCCATGCCTAGCTAATTTATGTGTTT T G HMGCL Ensembl:ENSG00000117305 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1020957727 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55703,RMVar_hsa_circ_360771 9438 RMVar_ID_9438 Human_SNP_ID_6362513 A-to-I Human chr1 - 23823421 23823421 23823421 TTGAACCTGGGAGGTGAAGGTTGCAGTGAGCCAAGATCGCGCCACTGCTCTCCAGCCTGGAGACA TTGAACCTGGGAGGTGAAGGTTGCAGTGAGCCGAGATCGCGCCACTGCTCTCCAGCCTGGAGACA T C HMGCL Ensembl:ENSG00000117305 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1306612123 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55703,RMVar_hsa_circ_360771 9439 RMVar_ID_9439 Human_SNP_ID_6374183 A-to-I Human chr1 - 23867997 23867997 23867997 GCCGCAGTACCAGCGCTTCATGCGCGACAACTACCCGCCCGGCTTCAGCTACGCCGACTTCGGAC GCCGCAGTACCAGCGCTTCATGCGCGACAACTGCCCGCCCGGCTTCAGCTACGCCGACTTCGGAC T C FUCA1 Ensembl:ENSG00000179163 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1328814351 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_30819 9440 RMVar_ID_9440 Human_SNP_ID_6375344 A-to-I Human chr1 - 23871989 23871989 23871989 AGCTGGGACTACAGGCACCCGCCACCACACTCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGT AGCTGGGACTACAGGCACCCGCCACCACACTCTGCTAATTTTTGTATTTTTAGTAGAGATGGGGT T A CNR2 Ensembl:ENSG00000188822 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2501417 Functional Loss SNV dbSNP153 33..33 33 - - - 9441 RMVar_ID_9441 Human_SNP_ID_6375345 A-to-I Human chr1 - 23871989 23871989 23871989 AGCTGGGACTACAGGCACCCGCCACCACACTCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGT AGCTGGGACTACAGGCACCCGCCACCACACTCGGCTAATTTTTGTATTTTTAGTAGAGATGGGGT T C CNR2 Ensembl:ENSG00000188822 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2501417 Functional Loss SNV dbSNP153 33..33 33 - - - 9442 RMVar_ID_9442 Human_SNP_ID_6375440 A-to-I Human chr1 - 23872314 23872314 23872314 CATAATTCTGGAGGCCAGAAGTCAAAATCAAGATGTGGTAGGGCCCTGCTCCCTCCAAAAGTTTA CATAATTCTGGAGGCCAGAAGTCAAAATCAAGGTGTGGTAGGGCCCTGCTCCCTCCAAAAGTTTA T C CNR2 Ensembl:ENSG00000188822 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6680132 Functional Loss SNV dbSNP153 33..33 33 - - - 9443 RMVar_ID_9443 Human_SNP_ID_6375441 A-to-I Human chr1 - 23872314 23872314 23872314 CATAATTCTGGAGGCCAGAAGTCAAAATCAAGATGTGGTAGGGCCCTGCTCCCTCCAAAAGTTTA CATAATTCTGGAGGCCAGAAGTCAAAATCAAGCTGTGGTAGGGCCCTGCTCCCTCCAAAAGTTTA T G CNR2 Ensembl:ENSG00000188822 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6680132 Functional Loss SNV dbSNP153 33..33 33 - - - 9444 RMVar_ID_9444 Human_SNP_ID_6375482 A-to-I Human chr1 - 23872551 23872551 23872551 AGTTCTGTTTGACTTCAAAGCCTGCCCTCTTAACCACTAACCTTTTGTCCTAGTTCAGTCAAATT AGTTCTGTTTGACTTCAAAGCCTGCCCTCTTAGCCACTAACCTTTTGTCCTAGTTCAGTCAAATT T C CNR2 Ensembl:ENSG00000188822 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2502996 Functional Loss SNV dbSNP153 33..33 33 - - - 9445 RMVar_ID_9445 Human_SNP_ID_6375748 A-to-I Human chr1 - 23873668 23873668 23873668 TGCCCCCAATTCAGCTCCCTTGCCTCCTCCACACCCCTATTACATATAATAAGCAGAGCAAGTGG TGCCCCCAATTCAGCTCCCTTGCCTCCTCCACTCCCCTATTACATATAATAAGCAGAGCAAGTGG T A CNR2 Ensembl:ENSG00000188822 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6665733 Functional Loss SNV dbSNP153 33..33 33 - - - 9446 RMVar_ID_9446 Human_SNP_ID_6375749 A-to-I Human chr1 - 23873668 23873668 23873668 TGCCCCCAATTCAGCTCCCTTGCCTCCTCCACACCCCTATTACATATAATAAGCAGAGCAAGTGG TGCCCCCAATTCAGCTCCCTTGCCTCCTCCACGCCCCTATTACATATAATAAGCAGAGCAAGTGG T C CNR2 Ensembl:ENSG00000188822 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6665733 Functional Loss SNV dbSNP153 33..33 33 - - - 9447 RMVar_ID_9447 Human_SNP_ID_6375750 A-to-I Human chr1 - 23873668 23873668 23873668 TGCCCCCAATTCAGCTCCCTTGCCTCCTCCACACCCCTATTACATATAATAAGCAGAGCAAGTGG TGCCCCCAATTCAGCTCCCTTGCCTCCTCCACCCCCCTATTACATATAATAAGCAGAGCAAGTGG T G CNR2 Ensembl:ENSG00000188822 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6665733 Functional Loss SNV dbSNP153 33..33 33 - - - 9448 RMVar_ID_9448 Human_SNP_ID_6375897 A-to-I Human chr1 - 23874310 23874310 23874310 TGGATAGGTAGGGCCACGAGGAGTAGCCAGGTAGGCGAGACACAAAAGGCCTGGGACAGGGTCAG TGGATAGGTAGGGCCACGAGGAGTAGCCAGGTGGGCGAGACACAAAAGGCCTGGGACAGGGTCAG T C CNR2 Ensembl:ENSG00000188822 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1105 Functional Loss SNV dbSNP153 33..33 33 - - - 9449 RMVar_ID_9449 Human_SNP_ID_6375951 A-to-I Human chr1 - 23874479 23874479 23874479 AACTCAAGTCAGAAATCAGTTCACTCCCTGGAAGAGAGAGAGGGGTCTTGGCACTCTCTTCTTAC AACTCAAGTCAGAAATCAGTTCACTCCCTGGAGGAGAGAGAGGGGTCTTGGCACTCTCTTCTTAC T C CNR2 Ensembl:ENSG00000188822 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2229584 Functional Loss SNV dbSNP153 33..33 33 - - - 9450 RMVar_ID_9450 Human_SNP_ID_6400869 A-to-I Human chr1 - 23974728 23974728 23974728 ACCTCCCGGGTTCAAATGATTCTTATGCCTCAACCTTCCGAGTAGCTGGGATTACAGGTGCATGC ACCTCCCGGGTTCAAATGATTCTTATGCCTCAGCCTTCCGAGTAGCTGGGATTACAGGTGCATGC T C SRSF10 Ensembl:ENSG00000188529 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1451200455 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10912,RMVar_hsa_circ_62178,RMVar_hsa_circ_315439,RMVar_hsa_circ_323665 9451 RMVar_ID_9451 Human_SNP_ID_6513488 A-to-I Human chr1 + 24426469 24426469 24426469 GGCGTGTGCCACCACCTCCAGCTAATTTTTGTATTGTTAGTAGAGACAGGGTTTCACCATGTTGA GGCGTGTGCCACCACCTCCAGCTAATTTTTGTGTTGTTAGTAGAGACAGGGTTTCACCATGTTGA A G NIPAL3 Ensembl:ENSG00000001461 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1274455230 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267183 9452 RMVar_ID_9452 Human_SNP_ID_6513870 A-to-I Human chr1 + 24428195 24428195 24428195 GCCAGAGATGGAGGTTGCAGTGAGCTGAGATCACGTCACTGCATTCCAGCCTCATTCCAGCCTGG GCCAGAGATGGAGGTTGCAGTGAGCTGAGATCCCGTCACTGCATTCCAGCCTCATTCCAGCCTGG A C NIPAL3 Ensembl:ENSG00000001461 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs930480745 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267183 9453 RMVar_ID_9453 Human_SNP_ID_6515565 A-to-I Human chr1 + 24435541 24435541 24435541 CCTTAATTTATAACAATCTAGTTCAGATTAACACCAACTTAATTTTAGTAGTACATGAAATGTCG CCTTAATTTATAACAATCTAGTTCAGATTAACGCCAACTTAATTTTAGTAGTACATGAAATGTCG A G NIPAL3 Ensembl:ENSG00000001461 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1401821730 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7092,RMVar_hsa_circ_267183,RMVar_hsa_circ_34100,RMVar_hsa_circ_130521 9454 RMVar_ID_9454 Human_SNP_ID_6524294 A-to-I Human chr1 + 24474150 24474150 24474150 AAGAAACTGAGACTGACTGGGCATGGTGGCTTATGCCTGTAATGCCACCACTTTGGGAGGCCAAG AAGAAACTGAGACTGACTGGGCATGGTGGCTTGTGCCTGTAATGCCACCACTTTGGGAGGCCAAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1137679 Functional Loss SNV dbSNP153 33..33 33 - - - 9455 RMVar_ID_9455 Human_SNP_ID_6524743 A-to-I Human chr1 + 24476161 24476161 24476161 TCGGTTCACTGCAACCTCCGCCTCCCGGGTTCAGGCGATTCTCCTGCCTCAGCCTCCCAAGTAGC TCGGTTCACTGCAACCTCCGCCTCCCGGGTTCGGGCGATTCTCCTGCCTCAGCCTCCCAAGTAGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1284184537 Functional Loss SNV dbSNP153 33..33 33 - - - 9456 RMVar_ID_9456 Human_SNP_ID_6539838 A-to-I Human chr1 + 24538428 24538427 24538429 ATTTTTATTTATTTATTTATTTATTTTGAGACAGAGTCTCACTCTGTCGCCCAGGCTGGAGCGCA ATTTTTATTTATTTATTTATTTATTTTGAGAC__AGTCTCACTCTGTCGCCCAGGCTGGAGCGCA CAG C RCAN3 Ensembl:ENSG00000117602 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1460371895 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_26377970 9457 RMVar_ID_9457 Human_SNP_ID_6539839 A-to-I Human chr1 + 24538428 24538428 24538428 ATTTTTATTTATTTATTTATTTATTTTGAGACAGAGTCTCACTCTGTCGCCCAGGCTGGAGCGCA ATTTTTATTTATTTATTTATTTATTTTGAGACGGAGTCTCACTCTGTCGCCCAGGCTGGAGCGCA A G RCAN3 Ensembl:ENSG00000117602 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1250492787 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26377970 9458 RMVar_ID_9458 Human_SNP_ID_6539937 A-to-I Human chr1 + 24538620 24538620 24538620 TTTTATAAGTAGAGACGGGGTTTCACCACGTTAGCCAGGATGGTCTCGATCTCCTGACCTAGTGA TTTTATAAGTAGAGACGGGGTTTCACCACGTTGGCCAGGATGGTCTCGATCTCCTGACCTAGTGA A G RCAN3 Ensembl:ENSG00000117602 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1245810184 Functional Loss SNV dbSNP153 33..33 33 - - - 9459 RMVar_ID_9459 Human_SNP_ID_6565959 A-to-I Human chr1 - 24641607 24641607 24641607 TTCCTTTACCTCGGCTTTCAAACCATCAAGAAACCCTCCCTGCTGTCATCGTGGTTCAGGGCACC TTCCTTTACCTCGGCTTTCAAACCATCAAGAAGCCCTCCCTGCTGTCATCGTGGTTCAGGGCACC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs549657749 Functional Loss SNV dbSNP153 33..33 33 - - - 9460 RMVar_ID_9460 Human_SNP_ID_6571089 A-to-I Human chr1 + 24659073 24659073 24659073 AAATTAGCCGGGCGTGGTTGGCGCATGCCTGTAATCCCAGCTACTCAGGTGGCTGAGGCAGGAGA AAATTAGCCGGGCGTGGTTGGCGCATGCCTGTGATCCCAGCTACTCAGGTGGCTGAGGCAGGAGA A G SRRM1 Ensembl:ENSG00000133226 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1013805195 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18621,RMVar_hsa_circ_62784,RMVar_hsa_circ_78311,RMVar_hsa_circ_51481,RMVar_hsa_circ_81919,RMVar_hsa_circ_70347,RMVar_hsa_circ_130532,RMVar_hsa_circ_365746,RMVar_hsa_circ_130533,RMVar_hsa_circ_29712,RMVar_hsa_circ_121590,RMVar_hsa_circ_130535 9461 RMVar_ID_9461 Human_SNP_ID_6572523 A-to-I Human chr1 + 24664257 24664257 24664257 AAGTCAGGTGATCCACCCGCCTCGGCCTCCCAAAGTGTTGGGATTACAGGCATGAGCCACTGGGC AAGTCAGGTGATCCACCCGCCTCGGCCTCCCAGAGTGTTGGGATTACAGGCATGAGCCACTGGGC A G SRRM1 Ensembl:ENSG00000133226 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs995283720 Functional Loss SNV dbSNP153 33..33 33 - - - 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 9462 RMVar_ID_9462 Human_SNP_ID_6572748 A-to-I Human chr1 + 24665171 24665171 24665171 GATAGAGGCCGGGTGCGGTGGCTCATGCCTGTAATCTCAGCACTTTGGGAGGCTGAGTTGGGTGG GATAGAGGCCGGGTGCGGTGGCTCATGCCTGTGATCTCAGCACTTTGGGAGGCTGAGTTGGGTGG A G SRRM1 Ensembl:ENSG00000133226 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886210981 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557670 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 9463 RMVar_ID_9463 Human_SNP_ID_6572911 A-to-I Human chr1 + 24665657 24665657 24665657 ATGGTGTGAACCCAGGAGGCAGAGCTTGCAGTAAGCCCAGATCGTGCCAGTGCACTCCAGCCTGG ATGGTGTGAACCCAGGAGGCAGAGCTTGCAGTGAGCCCAGATCGTGCCAGTGCACTCCAGCCTGG A G SRRM1 Ensembl:ENSG00000133226 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1442531222 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10897044 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 9464 RMVar_ID_9464 Human_SNP_ID_6575103 A-to-I Human chr1 + 24673444 24673444 24673444 TGTGATTGGAACATTTAGAATACTGGTGGGAGAAGTCCACCAGGCAAAGAGAACAGGATTGCAGT TGTGATTGGAACATTTAGAATACTGGTGGGAGGAGTCCACCAGGCAAAGAGAACAGGATTGCAGT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs937395009 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2140440 9465 RMVar_ID_9465 Human_SNP_ID_6575104 A-to-I Human chr1 + 24673444 24673444 24673444 TGTGATTGGAACATTTAGAATACTGGTGGGAGAAGTCCACCAGGCAAAGAGAACAGGATTGCAGT TGTGATTGGAACATTTAGAATACTGGTGGGAGTAGTCCACCAGGCAAAGAGAACAGGATTGCAGT A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs937395009 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2140440 9466 RMVar_ID_9466 Human_SNP_ID_6575367 A-to-I Human chr1 + 24674238 24674238 24674238 TTCCCTTTGCCTGGTGGACTTCTCCCACCAGTATTCTAAATGTTCCAATCACATGCTGAGACTTT TTCCCTTTGCCTGGTGGACTTCTCCCACCAGTGTTCTAAATGTTCCAATCACATGCTGAGACTTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041387899 Functional Loss SNV dbSNP153 33..33 33 - - - 9467 RMVar_ID_9467 Human_SNP_ID_6594459 A-to-I Human chr1 + 24745575 24745575 24745575 CCGAGCCGGCCATGGCGTTGTCGATGCCGCTGAATGGGCTGAAGGAGGAGGACAAAGAGCCCCTC CCGAGCCGGCCATGGCGTTGTCGATGCCGCTGTATGGGCTGAAGGAGGAGGACAAAGAGCCCCTC A T CLIC4 Ensembl:ENSG00000169504 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1434511274 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_349652,Human_RBP_ID_1427314,Human_RBP_ID_4092797,Human_RBP_ID_5799917,Human_RBP_ID_8754845,Human_RBP_ID_9319809,Human_RBP_ID_19034295,Human_RBP_ID_22430313 Human_Splice_Rec_31875,Human_Splice_Rec_31885,Human_Splice_Rec_31895,Human_Splice_Rec_31897 9468 RMVar_ID_9468 Human_SNP_ID_6596951 A-to-I Human chr1 + 24755035 24755035 24755035 CGGAGGTTGCAGTGAGCTGAGATTGTGTTACTACACTCCAGCCTGGACGACAGAGTAAGACTCCG CGGAGGTTGCAGTGAGCTGAGATTGTGTTACTGCACTCCAGCCTGGACGACAGAGTAAGACTCCG A G CLIC4 Ensembl:ENSG00000169504 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1365572030 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24675693 9469 RMVar_ID_9469 Human_SNP_ID_6597585 A-to-I Human chr1 + 24757122 24757122 24757122 TCTCCATGTTGGTCAAGCTAGTCTGTACCTCTAGACCTCAGGTGATCCGCCTGCCTCGGCCTCCC TCTCCATGTTGGTCAAGCTAGTCTGTACCTCTGGACCTCAGGTGATCCGCCTGCCTCGGCCTCCC A G CLIC4 Ensembl:ENSG00000169504 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1311929098 Functional Loss SNV dbSNP153 33..33 33 - - - 9470 RMVar_ID_9470 Human_SNP_ID_6598819 A-to-I Human chr1 + 24762356 24762356 24762356 GAGGCAGGAAGGTTCACTTGAACCCAGGAGTTAGAGGCTACGGTGAGATATGATCATGCCACTGC GAGGCAGGAAGGTTCACTTGAACCCAGGAGTTGGAGGCTACGGTGAGATATGATCATGCCACTGC A G CLIC4 Ensembl:ENSG00000169504 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1045883131 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5799986 9471 RMVar_ID_9471 Human_SNP_ID_6714351 A-to-I Human chr1 - 25220609 25220609 25220609 TTGCTGTGTCACCTAGGCTGGAGTGCAGTGGCACGATCTCGGCTCACTGCAACCTCCGCCTCCCG TTGCTGTGTCACCTAGGCTGGAGTGCAGTGGCCCGATCTCGGCTCACTGCAACCTCCGCCTCCCG T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1184859670 Functional Loss SNV dbSNP153 33..33 33 - - - 9472 RMVar_ID_9472 Human_SNP_ID_6716828 A-to-I Human chr1 - 25229949 25229949 25229949 AGCCAGGCATTGTGGCACACGCTTGTAACCCCAGCTACTCGGGAGGCTGAGGCATGAGAATTGTT AGCCAGGCATTGTGGCACACGCTTGTAACCCCGGCTACTCGGGAGGCTGAGGCATGAGAATTGTT T C SYF2 Ensembl:ENSG00000117614 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1211871767 Functional Loss SNV dbSNP153 33..33 33 - - - 9473 RMVar_ID_9473 Human_SNP_ID_6718009 A-to-I Human chr1 + 25233694 25233694 25233694 CAGGAGTTCAAGACCAGCCTGGACAACAAAGTAAGAATCAGTCTCTAAATTAAAAAATAAAAGTA CAGGAGTTCAAGACCAGCCTGGACAACAAAGTGAGAATCAGTCTCTAAATTAAAAAATAAAAGTA A G AL031432.4 Ensembl:ENSG00000284602 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs11249008 Functional Loss SNV dbSNP153 33..33 33 - - - 9474 RMVar_ID_9474 Human_SNP_ID_6718033 A-to-I Human chr1 + 25233768 25233768 25233768 TGTTTTTTTGTTTTGAGACAGAGTCTTGCACTATCACCCAGGCTGGAGTGCAGTGGCACCGATCT TGTTTTTTTGTTTTGAGACAGAGTCTTGCACTGTCACCCAGGCTGGAGTGCAGTGGCACCGATCT A G AL031432.4 Ensembl:ENSG00000284602 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1430859780 Functional Loss SNV dbSNP153 33..33 33 - - - 9475 RMVar_ID_9475 Human_SNP_ID_6733942 A-to-I Human chr1 + 25299827 25299827 25299827 GCTGGAGTGCAGTGGCGACATCTCAGCTCACTATAGCCTCCGCCTCCCAGGTTCCAGTGAATCTC GCTGGAGTGCAGTGGCGACATCTCAGCTCACTGTAGCCTCCGCCTCCCAGGTTCCAGTGAATCTC A G RHD Ensembl:ENSG00000187010 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444698967 Functional Loss SNV dbSNP153 33..33 33 - - - 9476 RMVar_ID_9476 Human_SNP_ID_6737456 A-to-I Human chr1 - 25315040 25315040 25315040 GCCACAACGCCCAGCTAATTTTTTGTATTTTTAGTAGGCACAGGGCTTCACCATGTTGGCCAGGA GCCACAACGCCCAGCTAATTTTTTGTATTTTTGGTAGGCACAGGGCTTCACCATGTTGGCCAGGA T C RSRP1 Ensembl:ENSG00000117616 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1318384663 Functional Loss SNV dbSNP153 33..33 33 - - - 9477 RMVar_ID_9477 Human_SNP_ID_6738167 A-to-I Human chr1 + 25318586 25318585 25318587 CTCCAGCCTAGGTGACAGAGTGAGACTGTCTCAAAAAAAAAAGAAAGAAAATATACATTCCATCC CTCCAGCCTAGGTGACAGAGTGAGACTGTCTC__AAAAAAAAGAAAGAAAATATACATTCCATCC CAA C RHD Ensembl:ENSG00000187010 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs532453902 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_32487 9478 RMVar_ID_9478 Human_SNP_ID_6743658 A-to-I Human chr1 + 25345988 25345988 25345988 TGTTTGTATTTTCTGTAGAGACGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGACCT TGTTTGTATTTTCTGTAGAGACGGGTTTCACCGTGTTGGCCAGGCTGGTCTTGAACTCCTGACCT A G TMEM50A Ensembl:ENSG00000183726 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1363431541 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99019,RMVar_hsa_circ_130553,RMVar_hsa_circ_270899,RMVar_hsa_circ_301031,RMVar_hsa_circ_296148,RMVar_hsa_circ_100049,RMVar_hsa_circ_130554,RMVar_hsa_circ_130555,RMVar_hsa_circ_130552,RMVar_hsa_circ_303047,RMVar_hsa_circ_130557,RMVar_hsa_circ_70829,RMVar_hsa_circ_130558 9479 RMVar_ID_9479 Human_SNP_ID_6743779 A-to-I Human chr1 + 25346473 25346473 25346473 CTGGAGTGCAAATGGTGTGATCATAACACACTACTGTCTCAAAATCCTGGGCTTAAGCAGTCCTC CTGGAGTGCAAATGGTGTGATCATAACACACTCCTGTCTCAAAATCCTGGGCTTAAGCAGTCCTC A C TMEM50A Ensembl:ENSG00000183726 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs537893868 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99019,RMVar_hsa_circ_130553,RMVar_hsa_circ_270899,RMVar_hsa_circ_301031,RMVar_hsa_circ_296148,RMVar_hsa_circ_100049,RMVar_hsa_circ_130554,RMVar_hsa_circ_130555,RMVar_hsa_circ_130552,RMVar_hsa_circ_303047,RMVar_hsa_circ_130557,RMVar_hsa_circ_70829,RMVar_hsa_circ_130558 9480 RMVar_ID_9480 Human_SNP_ID_6743805 A-to-I Human chr1 + 25346597 25346597 25346597 TTTAAACAGTTTTTTTGTAAAGACAGGATCTCACTATGTTGCCCAGGCTGTTCTTGAACTCCTGG TTTAAACAGTTTTTTTGTAAAGACAGGATCTCCCTATGTTGCCCAGGCTGTTCTTGAACTCCTGG A C TMEM50A Ensembl:ENSG00000183726 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1275423663 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99019,RMVar_hsa_circ_130553,RMVar_hsa_circ_270899,RMVar_hsa_circ_301031,RMVar_hsa_circ_296148,RMVar_hsa_circ_100049,RMVar_hsa_circ_130554,RMVar_hsa_circ_130555,RMVar_hsa_circ_130552,RMVar_hsa_circ_303047,RMVar_hsa_circ_130557,RMVar_hsa_circ_70829,RMVar_hsa_circ_130558 9481 RMVar_ID_9481 Human_SNP_ID_6743954 A-to-I Human chr1 + 25347259 25347259 25347259 TTCTGTAGACCTTTTTTTTTTTCTTTTGAGATAGGCTCTTGCTCTGTTGCCCAGGCTGGAGTGCA TTCTGTAGACCTTTTTTTTTTTCTTTTGAGATCGGCTCTTGCTCTGTTGCCCAGGCTGGAGTGCA A C TMEM50A Ensembl:ENSG00000183726 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1368455760 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99019,RMVar_hsa_circ_130553,RMVar_hsa_circ_270899,RMVar_hsa_circ_301031,RMVar_hsa_circ_296148,RMVar_hsa_circ_100049,RMVar_hsa_circ_130554,RMVar_hsa_circ_130555,RMVar_hsa_circ_130552,RMVar_hsa_circ_303047,RMVar_hsa_circ_130557,RMVar_hsa_circ_70829,RMVar_hsa_circ_130558 9482 RMVar_ID_9482 Human_SNP_ID_6744220 A-to-I Human chr1 + 25348574 25348574 25348574 GGGTGTGGTGACACGCGCCTGTGGTCCTAGCTACTCAGGAGGCTGAGGCAGGGGAATCGCTTGAA GGGTGTGGTGACACGCGCCTGTGGTCCTAGCTTCTCAGGAGGCTGAGGCAGGGGAATCGCTTGAA A T TMEM50A Ensembl:ENSG00000183726 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1391518631 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99019,RMVar_hsa_circ_130553,RMVar_hsa_circ_270899,RMVar_hsa_circ_301031,RMVar_hsa_circ_296148,RMVar_hsa_circ_100049,RMVar_hsa_circ_130554,RMVar_hsa_circ_130555,RMVar_hsa_circ_130552,RMVar_hsa_circ_303047,RMVar_hsa_circ_130557,RMVar_hsa_circ_70829,RMVar_hsa_circ_130558 9483 RMVar_ID_9483 Human_SNP_ID_6744662 A-to-I Human chr1 + 25350492 25350492 25350492 AGCTCACCACAACCTGTTTCCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGCTAGG AGCTCACCACAACCTGTTTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCTAGG A G TMEM50A Ensembl:ENSG00000183726 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1398311350 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99019,RMVar_hsa_circ_130553,RMVar_hsa_circ_270899,RMVar_hsa_circ_301031,RMVar_hsa_circ_296148,RMVar_hsa_circ_100049,RMVar_hsa_circ_130554,RMVar_hsa_circ_130555,RMVar_hsa_circ_130552,RMVar_hsa_circ_303047,RMVar_hsa_circ_130557,RMVar_hsa_circ_70829,RMVar_hsa_circ_130558 9484 RMVar_ID_9484 Human_SNP_ID_6746425 A-to-I Human chr1 + 25357814 25357814 25357814 CACACGCCACCACGCCTGGCTATTTTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGT CACACGCCACCACGCCTGGCTATTTTTTTTGTGTTTTTAGTAGAGACGGGGTTTCACCATGTTGT A G TMEM50A Ensembl:ENSG00000183726 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1244119968 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100049,RMVar_hsa_circ_130555 9485 RMVar_ID_9485 Human_SNP_ID_6766210 A-to-I Human chr1 + 25441270 25441270 25441270 TGGAGCTCAGTGGTATGATCTCGGCTCACTGTAACCTCCACCTCCTGGGTTCAAGCGATTCTCCT TGGAGCTCAGTGGTATGATCTCGGCTCACTGTGACCTCCACCTCCTGGGTTCAAGCGATTCTCCT A G MACO1 Ensembl:ENSG00000204178 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1429634110 Functional Loss SNV dbSNP153 33..33 33 - - - 9486 RMVar_ID_9486 Human_SNP_ID_6767074 A-to-I Human chr1 + 25445188 25445188 25445188 AAACATGGTGGCGCATGCCTATATTACCACCTACTTGGGAAGCTGAGGTAGAAGGATCACTTGAG AAACATGGTGGCGCATGCCTATATTACCACCTGCTTGGGAAGCTGAGGTAGAAGGATCACTTGAG A G MACO1 Ensembl:ENSG00000204178 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006842803 Functional Loss SNV dbSNP153 33..33 33 - - - 9487 RMVar_ID_9487 Human_SNP_ID_6768098 A-to-I Human chr1 + 25449604 25449603 25449605 GTTGCCCAGGCTGGACTTGAACTCCTGGGCTCAAATGATCCTCCCACCTCAGCCTCCTAAGTATC GTTGCCCAGGCTGGACTTGAACTCCTGGGCTC__ATGATCCTCCCACCTCAGCCTCCTAAGTATC CAA C MACO1 Ensembl:ENSG00000204178 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1431870818 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_130563,RMVar_hsa_circ_278489,RMVar_hsa_circ_330795,RMVar_hsa_circ_289623,RMVar_hsa_circ_130565,RMVar_hsa_circ_130566,RMVar_hsa_circ_130564,RMVar_hsa_circ_9358,RMVar_hsa_circ_299640,RMVar_hsa_circ_360059,RMVar_hsa_circ_317104,RMVar_hsa_circ_275668,RMVar_hsa_circ_130567,RMVar_hsa_circ_130568,RMVar_hsa_circ_130569 9488 RMVar_ID_9488 Human_SNP_ID_6769040 A-to-I Human chr1 + 25453408 25453408 25453408 TTTCTGGGCCGGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGCGG TTTCTGGGCCGGGCACGGTGGCTCACGCCTGTGATCCCAGCACTTTGGGAGGCTGAGGTGGGCGG A G MACO1 Ensembl:ENSG00000204178 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991359235 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_130563,RMVar_hsa_circ_278489,RMVar_hsa_circ_330795,RMVar_hsa_circ_289623,RMVar_hsa_circ_130565,RMVar_hsa_circ_130566,RMVar_hsa_circ_130564,RMVar_hsa_circ_9358,RMVar_hsa_circ_299640,RMVar_hsa_circ_360059,RMVar_hsa_circ_317104,RMVar_hsa_circ_275668,RMVar_hsa_circ_130567,RMVar_hsa_circ_130568,RMVar_hsa_circ_130569 9489 RMVar_ID_9489 Human_SNP_ID_6778761 A-to-I Human chr1 + 25493996 25493996 25493996 CTCGTGATCCACCCGCCTCGGCCTCCCAAAGTACTGGGATTACAGGCGTGAGCCACCGTGCCCGG CTCGTGATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGTGCCCGG A G MACO1 Ensembl:ENSG00000204178 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1044829901 Functional Loss SNV dbSNP153 33..33 33 - - - 9490 RMVar_ID_9490 Human_SNP_ID_6791807 A-to-I Human chr1 + 25548724 25548724 25548724 GAGACAAGGTCTCACTCTATTGCCCAGGCTGGAATGCAGTGATATGATCATAGCTTACTGCAGCC GAGACAAGGTCTCACTCTATTGCCCAGGCTGGCATGCAGTGATATGATCATAGCTTACTGCAGCC A C LDLRAP1 Ensembl:ENSG00000157978 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs974132932 Functional Loss SNV dbSNP153 33..33 33 - - - 9491 RMVar_ID_9491 Human_SNP_ID_6791826 A-to-I Human chr1 + 25548794 25548794 25548794 CTCCTGGGCTCAAGGGATCCTCCTGGGTAGCTAGAACTACAGGTGCACACTGCCACGCCCAGCTA CTCCTGGGCTCAAGGGATCCTCCTGGGTAGCTGGAACTACAGGTGCACACTGCCACGCCCAGCTA A G LDLRAP1 Ensembl:ENSG00000157978 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs1461075619 Functional Loss SNV dbSNP153 33..33 33 - - - 9492 RMVar_ID_9492 Human_SNP_ID_6791840 A-to-I Human chr1 + 25548846 25548846 25548846 CCACGCCCAGCTAATTATTTTTTGTAGAGACGAGGTCTTACCATGTTGTCCAGGCTGGTCTTGAA CCACGCCCAGCTAATTATTTTTTGTAGAGACGTGGTCTTACCATGTTGTCCAGGCTGGTCTTGAA A T LDLRAP1 Ensembl:ENSG00000157978 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041152010 Functional Loss SNV dbSNP153 33..33 33 - - - 9493 RMVar_ID_9493 Human_SNP_ID_6801804 A-to-I Human chr1 + 25587343 25587343 25587343 CCTGCTAATTTTATTTTTTATTTTGTAGAGACAGGGTCTTACCATGTTGCCCAGGGCTGGTTCTG CCTGCTAATTTTATTTTTTATTTTGTAGAGACGGGGTCTTACCATGTTGCCCAGGGCTGGTTCTG A G AL606491.1 Ensembl:ENSG00000225643 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1399528752 Functional Loss SNV dbSNP153 33..33 33 - - - 9494 RMVar_ID_9494 Human_SNP_ID_6853412 A-to-I Human chr1 + 25802076 25802075 25802076 GCAGTGGTGCAGTCACAGCTCACTGCAGCCTCAACTTCCCTGGCTCAATTGATCCTCCTGCCTCA GCAGTGGTGCAGTCACAGCTCACTGCAGCCTC_ACTTCCCTGGCTCAATTGATCCTCCTGCCTCA CA C SELENON Ensembl:ENSG00000162430 Protein coding intron GSE56152 embryonic stem cells,wild type - 25708366 RNA-Seq:(High) rs1199997242 Functional Loss DEL dbSNP153 33..33 33 - - - Human_Splice_Rec_32692,Human_Splice_Rec_32693 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_130587,RMVar_hsa_circ_11985,RMVar_hsa_circ_130586 9495 RMVar_ID_9495 Human_SNP_ID_6853822 A-to-I Human chr1 + 25803729 25803729 25803729 TTGTTTTTTTTGTTTTTTTGTTTTTTTTTTTGAGATGGAGTCTTGCTCTGTCACCCAGGCTGGAG TTGTTTTTTTTGTTTTTTTGTTTTTTTTTTTGTGATGGAGTCTTGCTCTGTCACCCAGGCTGGAG A T SELENON Ensembl:ENSG00000162430 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1359750167 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5908294 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_130587,RMVar_hsa_circ_11985,RMVar_hsa_circ_130586 9496 RMVar_ID_9496 Human_SNP_ID_6854149 A-to-I Human chr1 + 25804884 25804884 25804884 GGTTTCAATCCCGATTCCCCCACCATCTAGCTATGTGACCTGGGGAAGTGACTTTACCTCTCTGA GGTTTCAATCCCGATTCCCCCACCATCTAGCTGTGTGACCTGGGGAAGTGACTTTACCTCTCTGA A G SELENON Ensembl:ENSG00000162430 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1033647128 Functional Loss SNV dbSNP153 33..33 33 - - - 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_130587,RMVar_hsa_circ_11985,RMVar_hsa_circ_130586 9497 RMVar_ID_9497 Human_SNP_ID_6862122 A-to-I Human chr1 + 25832065 25832065 25832065 TCAGCTCTGCAAACTCAGTCTCATGCTCCTGGAATACCTTCAATAGCTGCCTTCCTCACCGCAGA TCAGCTCTGCAAACTCAGTCTCATGCTCCTGGCATACCTTCAATAGCTGCCTTCCTCACCGCAGA A C MTFR1L Ensembl:ENSG00000117640 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1051934134 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9358424,Human_RBP_ID_17217516,Human_RBP_ID_17747058,Human_RBP_ID_26797926 9498 RMVar_ID_9498 Human_SNP_ID_6864527 A-to-I Human chr1 - 25841652 25841652 25841652 GGGCGTGGTGGCCAGCACCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCGTGAA GGGCGTGGTGGCCAGCACCTGTAGTCCCAGCTGCTCGGGAGGCTGAGGCAGGAGAATGGCGTGAA T C AUNIP Ensembl:ENSG00000127423 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048608097 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_100982 9499 RMVar_ID_9499 Human_SNP_ID_6878774 A-to-I Human chr1 - 25900543 25900543 25900543 GTGCTGTTGGTGGCAGTGACTTCTTTTGAGTTAGGTTAATAAATCAAGCCATAGAGCCCCTCCTG GTGCTGTTGGTGGCAGTGACTTCTTTTGAGTTGGGTTAATAAATCAAGCCATAGAGCCCCTCCTG T C STMN1 Ensembl:ENSG00000117632 Protein coding intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1261168328 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_350117,Human_RBP_ID_3308168,Human_RBP_ID_8306550,Human_RBP_ID_8968174,Human_RBP_ID_18228423,Human_RBP_ID_23383029 9500 RMVar_ID_9500 Human_SNP_ID_6965075 A-to-I Human chr1 + 26244723 26244723 26244723 TTTGTGTGTTTTTATAGAGATGGCGTTTTGCCATGTTGCCCAGGCTGGTCTGGACTCCCAGACTC TTTGTGTGTTTTTATAGAGATGGCGTTTTGCCGTGTTGCCCAGGCTGGTCTGGACTCCCAGACTC A G CEP85 Ensembl:ENSG00000130695 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991115259 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10900759 RMVar_hsa_circ_10530,RMVar_hsa_circ_130622,RMVar_hsa_circ_115996,RMVar_hsa_circ_299728,RMVar_hsa_circ_46253,RMVar_hsa_circ_130623,RMVar_hsa_circ_336926,RMVar_hsa_circ_375296,RMVar_hsa_circ_130625,RMVar_hsa_circ_130626 9501 RMVar_ID_9501 Human_SNP_ID_6968130 A-to-I Human chr1 + 26256288 26256288 26256288 AAACCATCTTTGAGGCCAGGTGGCTCACGCCTATAATCCCAGCATTTTGGGAGGCCGAGGCGGGC AAACCATCTTTGAGGCCAGGTGGCTCACGCCTGTAATCCCAGCATTTTGGGAGGCCGAGGCGGGC A G CEP85 Ensembl:ENSG00000130695 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1292926445 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95267,RMVar_hsa_circ_130622,RMVar_hsa_circ_115996,RMVar_hsa_circ_299728,RMVar_hsa_circ_130623,RMVar_hsa_circ_336926,RMVar_hsa_circ_375296,RMVar_hsa_circ_130625,RMVar_hsa_circ_130626,RMVar_hsa_circ_293182,RMVar_hsa_circ_342467,RMVar_hsa_circ_123483,RMVar_hsa_circ_130627,RMVar_hsa_circ_130629,RMVar_hsa_circ_130630,RMVar_hsa_circ_130628 9502 RMVar_ID_9502 Human_SNP_ID_6968156 A-to-I Human chr1 + 26256424 26256424 26256424 GTGGTGGCATGCGCCTGTAGTCCCAACTACTCAGGAGGCTGTGGCAGGAGAATTGCTTGAACCTG GTGGTGGCATGCGCCTGTAGTCCCAACTACTCCGGAGGCTGTGGCAGGAGAATTGCTTGAACCTG A C CEP85 Ensembl:ENSG00000130695 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1024352698 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95267,RMVar_hsa_circ_130622,RMVar_hsa_circ_115996,RMVar_hsa_circ_299728,RMVar_hsa_circ_130623,RMVar_hsa_circ_336926,RMVar_hsa_circ_375296,RMVar_hsa_circ_130625,RMVar_hsa_circ_130626,RMVar_hsa_circ_293182,RMVar_hsa_circ_342467,RMVar_hsa_circ_123483,RMVar_hsa_circ_130627,RMVar_hsa_circ_130629,RMVar_hsa_circ_130630,RMVar_hsa_circ_130628 9503 RMVar_ID_9503 Human_SNP_ID_6968278 A-to-I Human chr1 + 26256849 26256849 26256849 TCGAACTCCTGACCTTGTGATCCGCCCGCCTCAGCCTCCGAAAGTGCTGGGATTACAGGGGTGAG TCGAACTCCTGACCTTGTGATCCGCCCGCCTCGGCCTCCGAAAGTGCTGGGATTACAGGGGTGAG A G CEP85 Ensembl:ENSG00000130695 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1236400321 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95267,RMVar_hsa_circ_130622,RMVar_hsa_circ_115996,RMVar_hsa_circ_299728,RMVar_hsa_circ_130623,RMVar_hsa_circ_336926,RMVar_hsa_circ_375296,RMVar_hsa_circ_130625,RMVar_hsa_circ_130626,RMVar_hsa_circ_293182,RMVar_hsa_circ_342467,RMVar_hsa_circ_123483,RMVar_hsa_circ_130627,RMVar_hsa_circ_130629,RMVar_hsa_circ_130630,RMVar_hsa_circ_130628 9504 RMVar_ID_9504 Human_SNP_ID_6969399 A-to-I Human chr1 + 26260816 26260813 26260817 TCCTGCCTTTCTTTTTTTTTTTTTTGAGATGGAATTTCGCTCTGGCATCTGGGCTGGAGTGCAGT TCCTGCCTTTCTTTTTTTTTTTTTTGAGAT____TTTCGCTCTGGCATCTGGGCTGGAGTGCAGT TGGAA T CEP85 Ensembl:ENSG00000130695 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1394776732 Functional Loss DEL dbSNP153 31..34 33 - - - RMVar_hsa_circ_95267,RMVar_hsa_circ_115996,RMVar_hsa_circ_130623,RMVar_hsa_circ_123483,RMVar_hsa_circ_130627,RMVar_hsa_circ_130628,RMVar_hsa_circ_95811,RMVar_hsa_circ_119831,RMVar_hsa_circ_130634,RMVar_hsa_circ_130635 9505 RMVar_ID_9505 Human_SNP_ID_6969404 A-to-I Human chr1 + 26260816 26260816 26260816 TCCTGCCTTTCTTTTTTTTTTTTTTGAGATGGAATTTCGCTCTGGCATCTGGGCTGGAGTGCAGT TCCTGCCTTTCTTTTTTTTTTTTTTGAGATGGTATTTCGCTCTGGCATCTGGGCTGGAGTGCAGT A T CEP85 Ensembl:ENSG00000130695 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1392239141 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95267,RMVar_hsa_circ_115996,RMVar_hsa_circ_130623,RMVar_hsa_circ_123483,RMVar_hsa_circ_130627,RMVar_hsa_circ_130628,RMVar_hsa_circ_95811,RMVar_hsa_circ_119831,RMVar_hsa_circ_130634,RMVar_hsa_circ_130635 9506 RMVar_ID_9506 Human_SNP_ID_6970558 A-to-I Human chr1 + 26265252 26265252 26265252 GTGATCTGCCCGCCTCGACTTCCCAAAGTGCTAGGATTACAGGCTTGAGCCACTGCACTGGCCTA GTGATCTGCCCGCCTCGACTTCCCAAAGTGCTGGGATTACAGGCTTGAGCCACTGCACTGGCCTA A G CEP85 Ensembl:ENSG00000130695 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1394786249 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95267,RMVar_hsa_circ_115996,RMVar_hsa_circ_130623,RMVar_hsa_circ_123483,RMVar_hsa_circ_130627,RMVar_hsa_circ_130628,RMVar_hsa_circ_95811,RMVar_hsa_circ_119831,RMVar_hsa_circ_130634,RMVar_hsa_circ_130635 9507 RMVar_ID_9507 Human_SNP_ID_6970711 A-to-I Human chr1 + 26265952 26265952 26265952 ATTTTAAGCCAGGCTCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGTGG ATTTTAAGCCAGGCTCGGTGGCTCACGCCTGTGATCCCAGCACTTTGGGAGGCCGAGGTGGGTGG A G CEP85 Ensembl:ENSG00000130695 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs888257184 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95267,RMVar_hsa_circ_115996,RMVar_hsa_circ_130623,RMVar_hsa_circ_123483,RMVar_hsa_circ_130627,RMVar_hsa_circ_130628,RMVar_hsa_circ_95811,RMVar_hsa_circ_119831,RMVar_hsa_circ_130634,RMVar_hsa_circ_130635 9508 RMVar_ID_9508 Human_SNP_ID_7015713 A-to-I Human chr1 + 26428712 26428712 26428712 TCAGGCACCCGCCACACTCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGT TCAGGCACCCGCCACACTCAGCTAATTTTTGTGTTTTTAGTAGAGACGGGGTTTCACCATGTTGT A G LIN28A Ensembl:ENSG00000131914 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1329446338 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107040,RMVar_hsa_circ_94681,RMVar_hsa_circ_122993,RMVar_hsa_circ_130647,RMVar_hsa_circ_89565,RMVar_hsa_circ_130648,RMVar_hsa_circ_130649,RMVar_hsa_circ_130650 9509 RMVar_ID_9509 Human_SNP_ID_7015717 A-to-I Human chr1 + 26428721 26428721 26428721 CGCCACACTCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGTCCAGGCTGG CGCCACACTCAGCTAATTTTTGTATTTTTAGTGGAGACGGGGTTTCACCATGTTGTCCAGGCTGG A G LIN28A Ensembl:ENSG00000131914 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1191888694 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107040,RMVar_hsa_circ_94681,RMVar_hsa_circ_122993,RMVar_hsa_circ_130647,RMVar_hsa_circ_89565,RMVar_hsa_circ_130648,RMVar_hsa_circ_130649,RMVar_hsa_circ_130650 9510 RMVar_ID_9510 Human_SNP_ID_7015764 A-to-I Human chr1 + 26428963 26428963 26428963 CTGAGGCGGGCGGATCACAAGGTCACGAGTTCAAAACTATCCTGGCCAACACAGTGAAACCCCGT CTGAGGCGGGCGGATCACAAGGTCACGAGTTCTAAACTATCCTGGCCAACACAGTGAAACCCCGT A T LIN28A Ensembl:ENSG00000131914 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1324747886 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107040,RMVar_hsa_circ_94681,RMVar_hsa_circ_122993,RMVar_hsa_circ_130647,RMVar_hsa_circ_89565,RMVar_hsa_circ_130648,RMVar_hsa_circ_130649,RMVar_hsa_circ_130650 9511 RMVar_ID_9511 Human_SNP_ID_7015767 A-to-I Human chr1 + 26428983 26428983 26428983 GGTCACGAGTTCAAAACTATCCTGGCCAACACAGTGAAACCCCGTCTCTACTAAAATACAAAAAA GGTCACGAGTTCAAAACTATCCTGGCCAACACGGTGAAACCCCGTCTCTACTAAAATACAAAAAA A G LIN28A Ensembl:ENSG00000131914 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1429765773 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_96906 RMVar_hsa_circ_107040,RMVar_hsa_circ_94681,RMVar_hsa_circ_122993,RMVar_hsa_circ_130647,RMVar_hsa_circ_89565,RMVar_hsa_circ_130648,RMVar_hsa_circ_130649,RMVar_hsa_circ_130650 9512 RMVar_ID_9512 Human_SNP_ID_7015774 A-to-I Human chr1 + 26429003 26429003 26429003 CCTGGCCAACACAGTGAAACCCCGTCTCTACTAAAATACAAAAAAATTAGCCGGGTGTGGTGGTG CCTGGCCAACACAGTGAAACCCCGTCTCTACTGAAATACAAAAAAATTAGCCGGGTGTGGTGGTG A G LIN28A Ensembl:ENSG00000131914 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1444777064 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107040,RMVar_hsa_circ_94681,RMVar_hsa_circ_122993,RMVar_hsa_circ_130647,RMVar_hsa_circ_89565,RMVar_hsa_circ_130648,RMVar_hsa_circ_130649,RMVar_hsa_circ_130650 9513 RMVar_ID_9513 Human_SNP_ID_7015779 A-to-I Human chr1 + 26429014 26429014 26429014 CAGTGAAACCCCGTCTCTACTAAAATACAAAAAAATTAGCCGGGTGTGGTGGTGCATGCCTTTAG CAGTGAAACCCCGTCTCTACTAAAATACAAAAGAATTAGCCGGGTGTGGTGGTGCATGCCTTTAG A G LIN28A Ensembl:ENSG00000131914 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1014257328 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107040,RMVar_hsa_circ_94681,RMVar_hsa_circ_122993,RMVar_hsa_circ_130647,RMVar_hsa_circ_89565,RMVar_hsa_circ_130648,RMVar_hsa_circ_130649,RMVar_hsa_circ_130650 9514 RMVar_ID_9514 Human_SNP_ID_7015781 A-to-I Human chr1 + 26429019 26429019 26429019 AAACCCCGTCTCTACTAAAATACAAAAAAATTAGCCGGGTGTGGTGGTGCATGCCTTTAGTCCTA AAACCCCGTCTCTACTAAAATACAAAAAAATTGGCCGGGTGTGGTGGTGCATGCCTTTAGTCCTA A G LIN28A Ensembl:ENSG00000131914 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1351955497 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107040,RMVar_hsa_circ_94681,RMVar_hsa_circ_122993,RMVar_hsa_circ_130647,RMVar_hsa_circ_89565,RMVar_hsa_circ_130648,RMVar_hsa_circ_130649,RMVar_hsa_circ_130650 9515 RMVar_ID_9515 Human_SNP_ID_7015794 A-to-I Human chr1 + 26429077 26429077 26429077 AGTCCTAGCTATTCAGGAGGCTGAGGCAGGGGAATCGCTTGAACCCGAGAGGCAGAGGTTGCAGT AGTCCTAGCTATTCAGGAGGCTGAGGCAGGGGTATCGCTTGAACCCGAGAGGCAGAGGTTGCAGT A T LIN28A Ensembl:ENSG00000131914 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs975659493 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107040,RMVar_hsa_circ_94681,RMVar_hsa_circ_122993,RMVar_hsa_circ_130647,RMVar_hsa_circ_89565,RMVar_hsa_circ_130648,RMVar_hsa_circ_130649,RMVar_hsa_circ_130650 9516 RMVar_ID_9516 Human_SNP_ID_7015798 A-to-I Human chr1 + 26429086 26429086 26429086 TATTCAGGAGGCTGAGGCAGGGGAATCGCTTGAACCCGAGAGGCAGAGGTTGCAGTGAGCTGAGA TATTCAGGAGGCTGAGGCAGGGGAATCGCTTGGACCCGAGAGGCAGAGGTTGCAGTGAGCTGAGA A G LIN28A Ensembl:ENSG00000131914 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs367858380 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107040,RMVar_hsa_circ_94681,RMVar_hsa_circ_122993,RMVar_hsa_circ_130647,RMVar_hsa_circ_89565,RMVar_hsa_circ_130648,RMVar_hsa_circ_130649,RMVar_hsa_circ_130650 9517 RMVar_ID_9517 Human_SNP_ID_7016775 A-to-I Human chr1 + 26433538 26433538 26433538 GGGCTTGGTGGTGTGCACCTGTAGTCCCAGCTACTCGGAAGGCTGAAGTGGGAGAATTTCTTGAG GGGCTTGGTGGTGTGCACCTGTAGTCCCAGCTGCTCGGAAGGCTGAAGTGGGAGAATTTCTTGAG A G DHDDS Ensembl:ENSG00000117682 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910643434 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22558239 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 9518 RMVar_ID_9518 Human_SNP_ID_7017404 A-to-I Human chr1 + 26436173 26436173 26436173 TAATCCCAGCACTTTGGGAGGCCAAATCGAGTAGATCTCTTGATCCCAGGAGTTCGAGAGCAGCC TAATCCCAGCACTTTGGGAGGCCAAATCGAGTGGATCTCTTGATCCCAGGAGTTCGAGAGCAGCC A G DHDDS Ensembl:ENSG00000117682 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1024600147 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 9519 RMVar_ID_9519 Human_SNP_ID_7018007 A-to-I Human chr1 + 26438469 26438469 26438469 GACATTGGCCAGACGTGGTTGCTTTTGCCTCTAATCCCACACTTTGGGAGGCCAAGGCAGGAGGA GACATTGGCCAGACGTGGTTGCTTTTGCCTCTGATCCCACACTTTGGGAGGCCAAGGCAGGAGGA A G DHDDS Ensembl:ENSG00000117682 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs961793830 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_44987 9520 RMVar_ID_9520 Human_SNP_ID_7018234 A-to-I Human chr1 + 26439523 26439523 26439523 AGGATGACTTGAACCCTGGAGGTTGAGGCTGCAGTGAGCTGTGTTCACGTCACCGCAATCCAACC AGGATGACTTGAACCCTGGAGGTTGAGGCTGCGGTGAGCTGTGTTCACGTCACCGCAATCCAACC A G DHDDS Ensembl:ENSG00000117682 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1466656910 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_44987 9521 RMVar_ID_9521 Human_SNP_ID_7018657 A-to-I Human chr1 + 26441360 26441360 26441360 AGCTGGGAATACAGGTGTGCGCCACCGCACCCAGCTAAGTTTCTGTATTTTTAGTAGAAATGGGG AGCTGGGAATACAGGTGTGCGCCACCGCACCCGGCTAAGTTTCTGTATTTTTAGTAGAAATGGGG A G DHDDS Ensembl:ENSG00000117682 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1247240049 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_44987 9522 RMVar_ID_9522 Human_SNP_ID_7018670 A-to-I Human chr1 + 26441397 26441396 26441397 AGTTTCTGTATTTTTAGTAGAAATGGGGTTTCACCATGTTGGCCAGGCTGGGCTTGAACTCCCAA AGTTTCTGTATTTTTAGTAGAAATGGGGTTTC_CCATGTTGGCCAGGCTGGGCTTGAACTCCCAA CA C DHDDS Ensembl:ENSG00000117682 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1395625457 Functional Loss DEL 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_44987 9523 RMVar_ID_9523 Human_SNP_ID_7018739 A-to-I Human chr1 + 26441775 26441775 26441775 AAAGTTAGCCAGATGTGGTGGCACATGCCTGTAGGCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAGTTAGCCAGATGTGGTGGCACATGCCTGTGGGCCCAGCTACTCGGGAGGCTGAGGCAGGAGA A G DHDDS Ensembl:ENSG00000117682 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs940702506 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_44987 9524 RMVar_ID_9524 Human_SNP_ID_7018748 A-to-I Human chr1 + 26441841 26441841 26441841 TCACTTGAACGTAGGAGGTGGAGGTTGTAGTGAGCCAAGATTGCACCACTGCACTCCAGCCTGGG TCACTTGAACGTAGGAGGTGGAGGTTGTAGTGGGCCAAGATTGCACCACTGCACTCCAGCCTGGG A G DHDDS Ensembl:ENSG00000117682 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1167387268 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_44987 9525 RMVar_ID_9525 Human_SNP_ID_7020115 A-to-I Human chr1 + 26447747 26447747 26447747 ATGGCAGCTCACGCCTGTAATCCTAGCACATTAGGAGGCCGAGGTGGGCAGTCCACTTGAGGCAG ATGGCAGCTCACGCCTGTAATCCTAGCACATTGGGAGGCCGAGGTGGGCAGTCCACTTGAGGCAG A G DHDDS Ensembl:ENSG00000117682 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1249375587 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86519,RMVar_hsa_circ_103558,RMVar_hsa_circ_130652,RMVar_hsa_circ_130653,RMVar_hsa_circ_325134,RMVar_hsa_circ_122380,RMVar_hsa_circ_44987,RMVar_hsa_circ_130654,RMVar_hsa_circ_323750,RMVar_hsa_circ_299923,RMVar_hsa_circ_130655,RMVar_hsa_circ_301288,RMVar_hsa_circ_130661,RMVar_hsa_circ_130658,RMVar_hsa_circ_130659,RMVar_hsa_circ_289512,RMVar_hsa_circ_320907,RMVar_hsa_circ_130662 9526 RMVar_ID_9526 Human_SNP_ID_7020255 A-to-I Human chr1 + 26448277 26448277 26448277 GGAGTTGCAACCTCCACCTCCCAGGTTCAAGCAATTCTTCCGCCTCAGCCTCCCAAGCAGCTGGG GGAGTTGCAACCTCCACCTCCCAGGTTCAAGCGATTCTTCCGCCTCAGCCTCCCAAGCAGCTGGG A G DHDDS Ensembl:ENSG00000117682 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1213251943 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86519,RMVar_hsa_circ_103558,RMVar_hsa_circ_130652,RMVar_hsa_circ_130653,RMVar_hsa_circ_325134,RMVar_hsa_circ_122380,RMVar_hsa_circ_44987,RMVar_hsa_circ_130654,RMVar_hsa_circ_323750,RMVar_hsa_circ_299923,RMVar_hsa_circ_130655,RMVar_hsa_circ_301288,RMVar_hsa_circ_130661,RMVar_hsa_circ_130658,RMVar_hsa_circ_130659,RMVar_hsa_circ_289512,RMVar_hsa_circ_320907,RMVar_hsa_circ_130662 9527 RMVar_ID_9527 Human_SNP_ID_7020269 A-to-I Human chr1 + 26448370 26448370 26448370 TAATTTTTGTATTTTCAGTCGAGACAGGTTTCACCATATTGGCCAGGCTAGTCTCGAACTCCTGA TAATTTTTGTATTTTCAGTCGAGACAGGTTTCGCCATATTGGCCAGGCTAGTCTCGAACTCCTGA A G DHDDS Ensembl:ENSG00000117682 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs968479851 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_34386 RMVar_hsa_circ_86519,RMVar_hsa_circ_103558,RMVar_hsa_circ_130652,RMVar_hsa_circ_130653,RMVar_hsa_circ_325134,RMVar_hsa_circ_122380,RMVar_hsa_circ_44987,RMVar_hsa_circ_130654,RMVar_hsa_circ_323750,RMVar_hsa_circ_299923,RMVar_hsa_circ_130655,RMVar_hsa_circ_301288,RMVar_hsa_circ_130661,RMVar_hsa_circ_130658,RMVar_hsa_circ_130659,RMVar_hsa_circ_289512,RMVar_hsa_circ_320907,RMVar_hsa_circ_130662 9528 RMVar_ID_9528 Human_SNP_ID_7020271 A-to-I Human chr1 + 26448387 26448387 26448387 GTCGAGACAGGTTTCACCATATTGGCCAGGCTAGTCTCGAACTCCTGACGTCGTGATCTGCCTGC GTCGAGACAGGTTTCACCATATTGGCCAGGCTGGTCTCGAACTCCTGACGTCGTGATCTGCCTGC A G DHDDS Ensembl:ENSG00000117682 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1294789855 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_34386 RMVar_hsa_circ_86519,RMVar_hsa_circ_103558,RMVar_hsa_circ_130652,RMVar_hsa_circ_130653,RMVar_hsa_circ_325134,RMVar_hsa_circ_122380,RMVar_hsa_circ_44987,RMVar_hsa_circ_130654,RMVar_hsa_circ_323750,RMVar_hsa_circ_299923,RMVar_hsa_circ_130655,RMVar_hsa_circ_301288,RMVar_hsa_circ_130661,RMVar_hsa_circ_130658,RMVar_hsa_circ_130659,RMVar_hsa_circ_289512,RMVar_hsa_circ_320907,RMVar_hsa_circ_130662 9529 RMVar_ID_9529 Human_SNP_ID_7021339 A-to-I Human chr1 + 26453007 26453007 26453007 GTAGCTACTTGGGAGGCTGAGTGAGGAGGATTACTTGAGCCTAGCAGGTCGAGGCTGCAATGAGC GTAGCTACTTGGGAGGCTGAGTGAGGAGGATTTCTTGAGCCTAGCAGGTCGAGGCTGCAATGAGC A T DHDDS Ensembl:ENSG00000117682 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs565572529 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86519,RMVar_hsa_circ_103558,RMVar_hsa_circ_130652,RMVar_hsa_circ_130653,RMVar_hsa_circ_325134,RMVar_hsa_circ_122380,RMVar_hsa_circ_44987,RMVar_hsa_circ_130654,RMVar_hsa_circ_323750,RMVar_hsa_circ_299923,RMVar_hsa_circ_130655,RMVar_hsa_circ_301288,RMVar_hsa_circ_130661,RMVar_hsa_circ_130658,RMVar_hsa_circ_130659,RMVar_hsa_circ_289512,RMVar_hsa_circ_320907,RMVar_hsa_circ_130662 9530 RMVar_ID_9530 Human_SNP_ID_7021783 A-to-I Human chr1 + 26454806 26454806 26454806 TGGGTTAATCCAACCATGAGCTCTGTAGGTCCAGCGGCACATCTTAGGTGCTTTGTTCACTTGGA TGGGTTAATCCAACCATGAGCTCTGTAGGTCCGGCGGCACATCTTAGGTGCTTTGTTCACTTGGA A G DHDDS Ensembl:ENSG00000117682 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs926729366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10901694 RMVar_hsa_circ_86519,RMVar_hsa_circ_103558,RMVar_hsa_circ_130652,RMVar_hsa_circ_130653,RMVar_hsa_circ_325134,RMVar_hsa_circ_122380,RMVar_hsa_circ_44987,RMVar_hsa_circ_130654,RMVar_hsa_circ_323750,RMVar_hsa_circ_299923,RMVar_hsa_circ_130655,RMVar_hsa_circ_301288,RMVar_hsa_circ_130661,RMVar_hsa_circ_130658,RMVar_hsa_circ_130659,RMVar_hsa_circ_289512,RMVar_hsa_circ_320907,RMVar_hsa_circ_130662 9531 RMVar_ID_9531 Human_SNP_ID_7025214 A-to-I Human chr1 + 26469626 26469625 26469627 ATTTGGGTAAGGAAAAAAGGGGTGGGAGAGACAGAAAATTTGCCCATCTGCTGCTCCTCCCCCTT ATTTGGGTAAGGAAAAAAGGGGTGGGAGAGAC__AAAATTTGCCCATCTGCTGCTCCTCCCCCTT CAG C DHDDS Ensembl:ENSG00000117682 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1362929751 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_18570413 Human_miRNA_ID_845190,Human_miRNA_ID_1383828 9532 RMVar_ID_9532 Human_SNP_ID_7025216 A-to-I Human chr1 + 26469629 26469627 26469630 TGGGTAAGGAAAAAAGGGGTGGGAGAGACAGAAAATTTGCCCATCTGCTGCTCCTCCCCCTTGGC TGGGTAAGGAAAAAAGGGGTGGGAGAGACAG___ATTTGCCCATCTGCTGCTCCTCCCCCTTGGC GAAA G DHDDS Ensembl:ENSG00000117682 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1301826659 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_18570413,Human_RBP_ID_22861144,Human_RBP_ID_26378330 Human_miRNA_ID_845190,Human_miRNA_ID_1383828 9533 RMVar_ID_9533 Human_SNP_ID_7026114 A-to-I Human chr1 + 26472488 26472488 26472488 CGGTCCGGGGCTCCCAGCGCTATAAAAACTTTATAAACCCCCCGGAGCCCGAGCAGTGTGAAGAA CGGTCCGGGGCTCCCAGCGCTATAAAAACTTTCTAAACCCCCCGGAGCCCGAGCAGTGTGAAGAA A C HMGN2 Ensembl:ENSG00000198830 Protein coding 5'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1243674126 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_350263,Human_RBP_ID_4073731,Human_RBP_ID_5413832,Human_RBP_ID_5433919,Human_RBP_ID_5457419,Human_RBP_ID_5485960,Human_RBP_ID_8968228,Human_RBP_ID_17747231,Human_RBP_ID_27396770 9534 RMVar_ID_9534 Human_SNP_ID_7026141 A-to-I Human chr1 + 26472527 26472527 26472527 CCCCGGAGCCCGAGCAGTGTGAAGAAGAGGCGAGAACGACCCCCGGACCGACCAAAGCCCGCGCG CCCCGGAGCCCGAGCAGTGTGAAGAAGAGGCGCGAACGACCCCCGGACCGACCAAAGCCCGCGCG A C HMGN2 Ensembl:ENSG00000198830 Protein coding 5'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1345350619 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224768,Human_RBP_ID_745835,Human_RBP_ID_9318722,Human_RBP_ID_9355796,Human_RBP_ID_10902024,Human_RBP_ID_18570419,Human_RBP_ID_22531926,Human_RBP_ID_26378350,Human_RBP_ID_27396771 9535 RMVar_ID_9535 Human_SNP_ID_7047308 A-to-I Human chr1 + 26549738 26549738 26549738 TTTTTTTCTTTCCCGAGATGGAGTCTCACTCTATCGCTCAGACTGGAGGGCAGTGGTGTGATCTC TTTTTTTCTTTCCCGAGATGGAGTCTCACTCTGTCGCTCAGACTGGAGGGCAGTGGTGTGATCTC A G RPS6KA1 Ensembl:ENSG00000117676 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs951970751 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18833 9536 RMVar_ID_9536 Human_SNP_ID_7047937 A-to-I Human chr1 + 26552186 26552186 26552186 CCGAGGTGGGCAGATCAGGAGGTCAGGAGATCAAGACCATCCTGCCCAACATGGTGAAACCCCGT CCGAGGTGGGCAGATCAGGAGGTCAGGAGATCGAGACCATCCTGCCCAACATGGTGAAACCCCGT A G RPS6KA1 Ensembl:ENSG00000117676 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1188866336 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110368,RMVar_hsa_circ_130671 9537 RMVar_ID_9537 Human_SNP_ID_7049961 A-to-I Human chr1 + 26559640 26559640 26559640 GACCTCAAGTGATCCGCCCACCTCAGCCTCCCAAGGTGCTGAGATTACAGACATGAGCACCTGAC GACCTCAAGTGATCCGCCCACCTCAGCCTCCCGAGGTGCTGAGATTACAGACATGAGCACCTGAC A G RPS6KA1 Ensembl:ENSG00000117676 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1054033168 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_130674,RMVar_hsa_circ_104483,RMVar_hsa_circ_130673 9538 RMVar_ID_9538 Human_SNP_ID_7050024 A-to-I Human chr1 + 26559969 26559969 26559969 CAAAAATCAGCTGGGCGTGTTGGCGCGTGCCTATAGTCCCAGCTACTTGGGAGGCAGAGGTTGCA CAAAAATCAGCTGGGCGTGTTGGCGCGTGCCTGTAGTCCCAGCTACTTGGGAGGCAGAGGTTGCA A G RPS6KA1 Ensembl:ENSG00000117676 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs752976698 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_130674,RMVar_hsa_circ_104483,RMVar_hsa_circ_130673 9539 RMVar_ID_9539 Human_SNP_ID_7050025 A-to-I Human chr1 + 26559971 26559971 26559971 AAAATCAGCTGGGCGTGTTGGCGCGTGCCTATAGTCCCAGCTACTTGGGAGGCAGAGGTTGCAGT AAAATCAGCTGGGCGTGTTGGCGCGTGCCTATGGTCCCAGCTACTTGGGAGGCAGAGGTTGCAGT A G RPS6KA1 Ensembl:ENSG00000117676 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs948257536 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_130674,RMVar_hsa_circ_104483,RMVar_hsa_circ_130673 9540 RMVar_ID_9540 Human_SNP_ID_7051024 A-to-I Human chr1 + 26563952 26563952 26563952 CAAGACCAGCTTGGCCAATATGATGAAACCCCATCTCTACCAAAAATACAAAAATTAGCTGGGCA CAAGACCAGCTTGGCCAATATGATGAAACCCCGTCTCTACCAAAAATACAAAAATTAGCTGGGCA A G RPS6KA1 Ensembl:ENSG00000117676 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1356331451 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104483,RMVar_hsa_circ_130673 9541 RMVar_ID_9541 Human_SNP_ID_7051030 A-to-I Human chr1 + 26564002 26563988 26564003 AAAATTAGCTGGGCATGGTGGCCCATGCCTGTAATCCCAGCTACTCTGGTGGCTGAGGCACAAGA AAAATTAGCTGGGCATGGCGGTGTGCGCCTGTAGTCCCAGCTACTCTGGTGGCTGAGGCACAAGA TGGCCCATGCCTGTAA CGGTGTGCGCCTGTAG RPS6KA1 Ensembl:ENSG00000117676 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs71576080 Functional Loss MNV dbSNP153 19..34 33 - - - RMVar_hsa_circ_104483,RMVar_hsa_circ_130673 9542 RMVar_ID_9542 Human_SNP_ID_7051137 A-to-I Human chr1 + 26564424 26564424 26564424 GGGACTACAGGCGCACACCGCCACACCCAGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTC GGGACTACAGGCGCACACCGCCACACCCAGCTGATTTTTTGTATTTTTAGTAGAGACGGGGTTTC A G RPS6KA1 Ensembl:ENSG00000117676 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1489454257 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104483,RMVar_hsa_circ_130673 9543 RMVar_ID_9543 Human_SNP_ID_7086840 A-to-I Human chr1 + 26704589 26704589 26704589 GGCCTTTAATACTGTTTTTGGCCGGGCGCGGTAGCTCACACCTATAATCCCAGCACTTTGGGAGG GGCCTTTAATACTGTTTTTGGCCGGGCGCGGTGGCTCACACCTATAATCCCAGCACTTTGGGAGG A G ARID1A Ensembl:ENSG00000117713 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs954681633 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223811,Human_RBP_ID_10903904 RMVar_hsa_circ_268846 9544 RMVar_ID_9544 Human_SNP_ID_7086844 A-to-I Human chr1 + 26704600 26704600 26704600 CTGTTTTTGGCCGGGCGCGGTAGCTCACACCTATAATCCCAGCACTTTGGGAGGCCAAGGTGGGA CTGTTTTTGGCCGGGCGCGGTAGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGA A G ARID1A Ensembl:ENSG00000117713 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs575700084 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223811,Human_RBP_ID_10903905,Human_RBP_ID_24763192 RMVar_hsa_circ_268846 9545 RMVar_ID_9545 Human_SNP_ID_7086882 A-to-I Human chr1 + 26704765 26704765 26704765 CTGTAGTCGCAGTTTACTTAGAAAGCTGAGGCAGGAGGATTGCTTGAGCCCAGGAGGTTGAGGCT CTGTAGTCGCAGTTTACTTAGAAAGCTGAGGCGGGAGGATTGCTTGAGCCCAGGAGGTTGAGGCT A G ARID1A Ensembl:ENSG00000117713 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1401900179 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10903909 RMVar_hsa_circ_268846 9546 RMVar_ID_9546 Human_SNP_ID_7086887 A-to-I Human chr1 + 26704784 26704784 26704784 AGAAAGCTGAGGCAGGAGGATTGCTTGAGCCCAGGAGGTTGAGGCTGTTGTAAGCCATGATTACG AGAAAGCTGAGGCAGGAGGATTGCTTGAGCCCGGGAGGTTGAGGCTGTTGTAAGCCATGATTACG A G ARID1A Ensembl:ENSG00000117713 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs996124829 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268846 9547 RMVar_ID_9547 Human_SNP_ID_7088898 A-to-I Human chr1 + 26711246 26711246 26711246 TTTTCCTGCCTCAGCCTCTCGTAGCTGGGATTACAGGTCCACGCCACCACGCCCGGCTAATTTTA TTTTCCTGCCTCAGCCTCTCGTAGCTGGGATTCCAGGTCCACGCCACCACGCCCGGCTAATTTTA A C ARID1A Ensembl:ENSG00000117713 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1234999116 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268846 9548 RMVar_ID_9548 Human_SNP_ID_7088919 A-to-I Human chr1 + 26711303 26711303 26711303 TAATTTTATTTATTTATTTATATATATTTTTTAGTAGAGACGAGATTTCACCATGTTGGCCATGC TAATTTTATTTATTTATTTATATATATTTTTTCGTAGAGACGAGATTTCACCATGTTGGCCATGC A C ARID1A Ensembl:ENSG00000117713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1398452433 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5802291,Human_RBP_ID_10904137 RMVar_hsa_circ_268846 9549 RMVar_ID_9549 Human_SNP_ID_7089103 A-to-I Human chr1 + 26711961 26711961 26711961 AAAATCAGCCAGGCATGGTGATGCGCGCCTGTAGTCTCAGCTACGTGGGGGCTGAGATGGGAGGA AAAATCAGCCAGGCATGGTGATGCGCGCCTGTGGTCTCAGCTACGTGGGGGCTGAGATGGGAGGA A G ARID1A Ensembl:ENSG00000117713 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1296945794 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10904167,Human_RBP_ID_18570534 RMVar_hsa_circ_268846 9550 RMVar_ID_9550 Human_SNP_ID_7089243 A-to-I Human chr1 + 26712498 26712498 26712498 CTTGAGCCCAGGAGTTCGAGACCAGCCTTGGCAACATAGCAAGACCTTGTCTCTCTTAAAAAAAA CTTGAGCCCAGGAGTTCGAGACCAGCCTTGGCCACATAGCAAGACCTTGTCTCTCTTAAAAAAAA A C ARID1A Ensembl:ENSG00000117713 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1293449275 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268846 9551 RMVar_ID_9551 Human_SNP_ID_7090112 A-to-I Human chr1 + 26715987 26715987 26715987 CCAGTACTTGGGGAGACTGAGGTGGGCGGATCATGAGGTCAGGAGTTTGAGACCAGCCTTATCAA CCAGTACTTGGGGAGACTGAGGTGGGCGGATCGTGAGGTCAGGAGTTTGAGACCAGCCTTATCAA A G ARID1A Ensembl:ENSG00000117713 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1203499611 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268846 9552 RMVar_ID_9552 Human_SNP_ID_7090308 A-to-I Human chr1 + 26716719 26716719 26716719 GTGGTCTCAGCTCACTGCAGCCACTGCCTCCCAGGTTCAAACCATTCTCCTGCCTCAGCCTCCCG GTGGTCTCAGCTCACTGCAGCCACTGCCTCCCGGGTTCAAACCATTCTCCTGCCTCAGCCTCCCG A G ARID1A Ensembl:ENSG00000117713 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs918963377 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268846 9553 RMVar_ID_9553 Human_SNP_ID_7090603 A-to-I Human chr1 + 26717995 26717995 26717995 GTTGTTATTTATTTTTGTTGTTGTTGTTTCTGAGATGAAGTTTGCTCTGTTGCTCAGGCTGGAGT GTTGTTATTTATTTTTGTTGTTGTTGTTTCTGTGATGAAGTTTGCTCTGTTGCTCAGGCTGGAGT A T ARID1A Ensembl:ENSG00000117713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232741732 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3308393,Human_RBP_ID_5802392,Human_RBP_ID_10904452 RMVar_hsa_circ_268846 9554 RMVar_ID_9554 Human_SNP_ID_7091218 A-to-I Human chr1 + 26720089 26720088 26720089 CCTGACCAACATGGTGAAACCCCGTTGCTACTAAAAATACAAAAATTAGCCGGGCATGGTGGCAT CCTGACCAACATGGTGAAACCCCGTTGCTACT_AAAATACAAAAATTAGCCGGGCATGGTGGCAT TA T ARID1A Ensembl:ENSG00000117713 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1240300065 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_268846 9555 RMVar_ID_9555 Human_SNP_ID_7091237 A-to-I Human chr1 + 26720144 26720144 26720144 ATGGTGGCATGCACCTGTAATCTCAGCTACTCAGGAGGTTGAGGTAGGAGAATTGCTTGAACCCG ATGGTGGCATGCACCTGTAATCTCAGCTACTCGGGAGGTTGAGGTAGGAGAATTGCTTGAACCCG A G ARID1A Ensembl:ENSG00000117713 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1485117549 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268846 9556 RMVar_ID_9556 Human_SNP_ID_7091298 A-to-I Human chr1 + 26720344 26720344 26720344 AAAATAAAAAAATTAGCAGGCCCTGGTGGCACAGGTCTGTAATCCCAACTGCTAGGGTGACTGTG AAAATAAAAAAATTAGCAGGCCCTGGTGGCACGGGTCTGTAATCCCAACTGCTAGGGTGACTGTG A G ARID1A Ensembl:ENSG00000117713 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1194646111 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268846 9557 RMVar_ID_9557 Human_SNP_ID_7091557 A-to-I Human chr1 + 26721243 26721239 26721243 TTGTTTTTGTTTTTGTTTTGAGACCGAGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGTGCG TTGTTTTTGTTTTTGTTTTGAGACCGAGT____CTCTGTCACCCAGGCTGGAGTGCAGTGGTGCG TCTCA T ARID1A Ensembl:ENSG00000117713 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs952914682 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_268846 9558 RMVar_ID_9558 Human_SNP_ID_7091581 A-to-I Human chr1 + 26721311 26721311 26721311 TCGGCTCACTGTGACCTCCACCTCCCAGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGC TCGGCTCACTGTGACCTCCACCTCCCAGGTTCCAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGC A C ARID1A Ensembl:ENSG00000117713 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1350760124 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268846 9559 RMVar_ID_9559 Human_SNP_ID_7091589 A-to-I Human chr1 + 26721351 26721351 26721351 CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCGCGTGCCATCACACCCGGCTAATATTT CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTGCAGGCGCGTGCCATCACACCCGGCTAATATTT A G ARID1A Ensembl:ENSG00000117713 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1251633169 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268846 9560 RMVar_ID_9560 Human_SNP_ID_7091603 A-to-I Human chr1 + 26721392 26721392 26721392 TGCCATCACACCCGGCTAATATTTGTATTTTCAGTAGAGACCAGGTTTCACCATATTGGCCAGGC TGCCATCACACCCGGCTAATATTTGTATTTTCGGTAGAGACCAGGTTTCACCATATTGGCCAGGC A G ARID1A Ensembl:ENSG00000117713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1411392728 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268846 9561 RMVar_ID_9561 Human_SNP_ID_7095333 A-to-I Human chr1 + 26736258 26736258 26736258 AGGCAAGAGAATCACTTTAGAACCTGGGAGGCAGAGGTTGCATTGAGCCGAGATCACACCACTGC AGGCAAGAGAATCACTTTAGAACCTGGGAGGCGGAGGTTGCATTGAGCCGAGATCACACCACTGC A G ARID1A Ensembl:ENSG00000117713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs981103987 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10905158,Human_RBP_ID_22470022 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 9562 RMVar_ID_9562 Human_SNP_ID_7095505 A-to-I Human chr1 + 26736834 26736791 26736835 TGAGGCAGGAGAATTGCTTCAATCCAGGAGGCAGAGGTTGCAGTGAGCCAAGATCACGCCATTGC __________________________________AGGTTGCAGTGAGCCAAGATCACGCCATTGC ACTCGGGAGGCTGAGGCAGGAGAATTGCTTCAATCCAGGAGGCAG A ARID1A Ensembl:ENSG00000117713 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1209479042 Functional Loss DEL dbSNP153 1..34 33 - - - 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 9563 RMVar_ID_9563 Human_SNP_ID_7095641 A-to-I Human chr1 + 26737210 26737210 26737210 TATTCTCGGCTCACTGCAGTCTCCACCTCCCCAGGTTCAGGTGATCCTCCCACCTCAGCCTCCTG TATTCTCGGCTCACTGCAGTCTCCACCTCCCCGGGTTCAGGTGATCCTCCCACCTCAGCCTCCTG A G ARID1A Ensembl:ENSG00000117713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1238550599 Functional Loss SNV dbSNP153 33..33 33 - - - 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 9564 RMVar_ID_9564 Human_SNP_ID_7095646 A-to-I Human chr1 + 26737234 26737234 26737234 ACCTCCCCAGGTTCAGGTGATCCTCCCACCTCAGCCTCCTGAGTAGCTGGGACTACAGGTGTGAG ACCTCCCCAGGTTCAGGTGATCCTCCCACCTCTGCCTCCTGAGTAGCTGGGACTACAGGTGTGAG A T ARID1A Ensembl:ENSG00000117713 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs891083352 Functional Loss SNV dbSNP153 33..33 33 - - - 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 9565 RMVar_ID_9565 Human_SNP_ID_7095886 A-to-I Human chr1 + 26738163 26738162 26738164 CTCCTGCCTCAGCCTCCCAGGTAGCTGGAATTACAGACGCCCGCTACCACACCCGGCTAATTTTT CTCCTGCCTCAGCCTCCCAGGTAGCTGGAATT__AGACGCCCGCTACCACACCCGGCTAATTTTT TAC T ARID1A Ensembl:ENSG00000117713 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1020107645 Functional Loss DEL dbSNP153 33..34 33 - - - 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 9566 RMVar_ID_9566 Human_SNP_ID_7101272 A-to-I Human chr1 + 26759242 26759242 26759242 TGTTTGTTTTTGAGATGGTGTTTTGCTCCGTTACCTATGCTGGAGTGCAGTGGTACAATCTCGGC TGTTTGTTTTTGAGATGGTGTTTTGCTCCGTTGCCTATGCTGGAGTGCAGTGGTACAATCTCGGC A G ARID1A Ensembl:ENSG00000117713 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs778742298 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23383495 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 9567 RMVar_ID_9567 Human_SNP_ID_7102518 A-to-I Human chr1 + 26763694 26763694 26763694 GGGAGGCTGAGGCAGGAGAATCACTTGAACCCAGGAGGAAGAGGTTGCAGTGAGCCAAGACTGCG GGGAGGCTGAGGCAGGAGAATCACTTGAACCCGGGAGGAAGAGGTTGCAGTGAGCCAAGACTGCG A G ARID1A Ensembl:ENSG00000117713 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1204888635 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49434,RMVar_hsa_circ_130679,RMVar_hsa_circ_109031,RMVar_hsa_circ_266788,RMVar_hsa_circ_95019,RMVar_hsa_circ_130680,RMVar_hsa_circ_61331,RMVar_hsa_circ_25221,RMVar_hsa_circ_50375 9568 RMVar_ID_9568 Human_SNP_ID_7102583 A-to-I Human chr1 + 26763928 26763928 26763928 CTCCCACCTCAGCCTTCTGAGTAGTTGGGACTACAGGCACACACCACCACACCCAGCTAATTTTT CTCCCACCTCAGCCTTCTGAGTAGTTGGGACTGCAGGCACACACCACCACACCCAGCTAATTTTT A G ARID1A Ensembl:ENSG00000117713 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1429533522 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49434,RMVar_hsa_circ_130679,RMVar_hsa_circ_109031,RMVar_hsa_circ_266788,RMVar_hsa_circ_95019,RMVar_hsa_circ_130680,RMVar_hsa_circ_61331,RMVar_hsa_circ_25221,RMVar_hsa_circ_50375 9569 RMVar_ID_9569 Human_SNP_ID_7102600 A-to-I Human chr1 + 26764001 26763997 26764001 TTATATTTATTTATTTATTTAGAGACTGTCTCACTCTGTTGCCCAAGCTGGAGTGTAATGGCACA TTATATTTATTTATTTATTTAGAGACTGT____CTCTGTTGCCCAAGCTGGAGTGTAATGGCACA TCTCA T ARID1A Ensembl:ENSG00000117713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1376995215 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_49434,RMVar_hsa_circ_130679,RMVar_hsa_circ_109031,RMVar_hsa_circ_266788,RMVar_hsa_circ_95019,RMVar_hsa_circ_130680,RMVar_hsa_circ_61331,RMVar_hsa_circ_25221,RMVar_hsa_circ_50375 9570 RMVar_ID_9570 Human_SNP_ID_7102601 A-to-I Human chr1 + 26764001 26764001 26764001 TTATATTTATTTATTTATTTAGAGACTGTCTCACTCTGTTGCCCAAGCTGGAGTGTAATGGCACA TTATATTTATTTATTTATTTAGAGACTGTCTCTCTCTGTTGCCCAAGCTGGAGTGTAATGGCACA A T ARID1A Ensembl:ENSG00000117713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs755364723 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49434,RMVar_hsa_circ_130679,RMVar_hsa_circ_109031,RMVar_hsa_circ_266788,RMVar_hsa_circ_95019,RMVar_hsa_circ_130680,RMVar_hsa_circ_61331,RMVar_hsa_circ_25221,RMVar_hsa_circ_50375 9571 RMVar_ID_9571 Human_SNP_ID_7102644 A-to-I Human chr1 + 26764165 26764165 26764165 CTAATTTTTATATTTTTAGACTGGGTTTCACCATGTTAGCCAGGCTGGTCTCAAAATCCTGACCT CTAATTTTTATATTTTTAGACTGGGTTTCACCGTGTTAGCCAGGCTGGTCTCAAAATCCTGACCT A G ARID1A Ensembl:ENSG00000117713 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1206725817 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49434,RMVar_hsa_circ_130679,RMVar_hsa_circ_109031,RMVar_hsa_circ_266788,RMVar_hsa_circ_95019,RMVar_hsa_circ_130680,RMVar_hsa_circ_61331,RMVar_hsa_circ_25221,RMVar_hsa_circ_50375 9572 RMVar_ID_9572 Human_SNP_ID_7103071 A-to-I Human chr1 + 26765821 26765821 26765821 GGGAGGCTGAGATTGCAGTGAGCCGAGATTTCACCATTGCACTCCAGCCTGGGCAACAAGAGTGA GGGAGGCTGAGATTGCAGTGAGCCGAGATTTCGCCATTGCACTCCAGCCTGGGCAACAAGAGTGA A G ARID1A Ensembl:ENSG00000117713 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4970484 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49434,RMVar_hsa_circ_130679,RMVar_hsa_circ_109031,RMVar_hsa_circ_266788,RMVar_hsa_circ_95019,RMVar_hsa_circ_130680,RMVar_hsa_circ_61331,RMVar_hsa_circ_25221,RMVar_hsa_circ_50375 9573 RMVar_ID_9573 Human_SNP_ID_7105989 A-to-I Human chr1 + 26776455 26776455 26776455 GCCACCACGCTCGGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGA GCCACCACGCTCGGCTAATTTTTTGTATTTTTGGTAGAGACGGGGTTTCACCGTGTTAGCCAGGA A G ARID1A Ensembl:ENSG00000117713 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1318777864 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266788 9574 RMVar_ID_9574 Human_SNP_ID_7106183 A-to-I Human chr1 + 26777269 26777269 26777269 TATTTTGAGACAGGGTCTCCATTACTCAAGCTAGAGTGCAGTGGTGCAATCACAGCTCACTGCAG TATTTTGAGACAGGGTCTCCATTACTCAAGCTGGAGTGCAGTGGTGCAATCACAGCTCACTGCAG A G ARID1A Ensembl:ENSG00000117713 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1232739619 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266788 9575 RMVar_ID_9575 Human_SNP_ID_7106246 A-to-I Human chr1 + 26777484 26777484 26777484 AAACTCCTGGGCTCAAGTGATTGACCTACCTCAGCCTCTCAAAGTACTAGGATTACAGGTGTGAG AAACTCCTGGGCTCAAGTGATTGACCTACCTCGGCCTCTCAAAGTACTAGGATTACAGGTGTGAG A G ARID1A Ensembl:ENSG00000117713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1274729105 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266788 9576 RMVar_ID_9576 Human_SNP_ID_7106275 A-to-I Human chr1 + 26777602 26777602 26777602 CACTGTGTTGCCCAGGCTGGTCTCAAACTCCTAGGCTCAAGTGATTCTCCCACTTCAACCTTCCA CACTGTGTTGCCCAGGCTGGTCTCAAACTCCTGGGCTCAAGTGATTCTCCCACTTCAACCTTCCA A G ARID1A Ensembl:ENSG00000117713 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1458876865 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266788 9577 RMVar_ID_9577 Human_SNP_ID_7111367 A-to-I Human chr1 + 26795958 26795958 26795958 TCAGCTCACTGCAACCTGTGTCTCCTGGGTTCAAGCGACTCTTCTGCCTCAATCTCCCGAGTAGC TCAGCTCACTGCAACCTGTGTCTCCTGGGTTCTAGCGACTCTTCTGCCTCAATCTCCCGAGTAGC A T PIGV Ensembl:ENSG00000060642 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1396172969 Functional Loss SNV dbSNP153 33..33 33 - - - 9578 RMVar_ID_9578 Human_SNP_ID_7132365 A-to-I Human chr1 - 26876298 26876298 26876298 GGCAGGAGAATCGCTTGAACCTGGGAGGCGGAAGTTTCAGTGAGCGGAGATCGCGCCATTGCACT GGCAGGAGAATCGCTTGAACCTGGGAGGCGGACGTTTCAGTGAGCGGAGATCGCGCCATTGCACT T G GPN2 Ensembl:ENSG00000142751 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1176307725 Functional Loss SNV dbSNP153 33..33 33 - - - 9579 RMVar_ID_9579 Human_SNP_ID_7132379 A-to-I Human chr1 - 26876327 26876327 26876327 CCTGTAATTCCAGCTACTTAGGAGACTGAGGCAGGAGAATCGCTTGAACCTGGGAGGCGGAAGTT CCTGTAATTCCAGCTACTTAGGAGACTGAGGCGGGAGAATCGCTTGAACCTGGGAGGCGGAAGTT T C GPN2 Ensembl:ENSG00000142751 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs373584768 Functional Loss SNV dbSNP153 33..33 33 - - - 9580 RMVar_ID_9580 Human_SNP_ID_7132380 A-to-I Human chr1 - 26876344 26876344 26876344 GGGCATGGTGGCATGCGCCTGTAATTCCAGCTACTTAGGAGACTGAGGCAGGAGAATCGCTTGAA GGGCATGGTGGCATGCGCCTGTAATTCCAGCTCCTTAGGAGACTGAGGCAGGAGAATCGCTTGAA T G GPN2 Ensembl:ENSG00000142751 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1460981596 Functional Loss SNV dbSNP153 33..33 33 - - - 9581 RMVar_ID_9581 Human_SNP_ID_7132381 A-to-I Human chr1 - 26876354 26876354 26876354 AAAATGAGCAGGGCATGGTGGCATGCGCCTGTAATTCCAGCTACTTAGGAGACTGAGGCAGGAGA AAAATGAGCAGGGCATGGTGGCATGCGCCTGTGATTCCAGCTACTTAGGAGACTGAGGCAGGAGA T C GPN2 Ensembl:ENSG00000142751 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1134228 Functional Loss SNV dbSNP153 33..33 33 - - - 9582 RMVar_ID_9582 Human_SNP_ID_7132681 A-to-I Human chr1 - 26877792 26877792 26877792 TGACCTCATGATTTACCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCAC TGACCTCATGATTTACCCGCCTTGGCCTCCCATAGTGCTGGGATTACAGGCGTGAGCCACTGCAC T A GPN2 Ensembl:ENSG00000142751 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913749159 Functional Loss SNV dbSNP153 33..33 33 - - - 9583 RMVar_ID_9583 Human_SNP_ID_7132682 A-to-I Human chr1 - 26877792 26877792 26877792 TGACCTCATGATTTACCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCAC TGACCTCATGATTTACCCGCCTTGGCCTCCCAGAGTGCTGGGATTACAGGCGTGAGCCACTGCAC T C GPN2 Ensembl:ENSG00000142751 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913749159 Functional Loss SNV dbSNP153 33..33 33 - - - 9584 RMVar_ID_9584 Human_SNP_ID_7132728 A-to-I Human chr1 - 26877985 26877985 26877985 CTCTGTCGCCCAGGCTGGAGTCCAGTGGCACAATCTCGGCTCACTGCAACCTCCGCCTCCCAGGT CTCTGTCGCCCAGGCTGGAGTCCAGTGGCACAGTCTCGGCTCACTGCAACCTCCGCCTCCCAGGT T C GPN2 Ensembl:ENSG00000142751 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs189520359 Functional Loss SNV dbSNP153 33..33 33 - - - 9585 RMVar_ID_9585 Human_SNP_ID_7132744 A-to-I Human chr1 - 26878028 26878028 26878028 TTTGCATGTATTTGGACTTTCTTTTTTTGGAGACAAAGTCTCTCTCTGTCGCCCAGGCTGGAGTC TTTGCATGTATTTGGACTTTCTTTTTTTGGAGTCAAAGTCTCTCTCTGTCGCCCAGGCTGGAGTC T A GPN2 Ensembl:ENSG00000142751 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs960200243 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10906129,Human_RBP_ID_17747412,Human_RBP_ID_22783734 9586 RMVar_ID_9586 Human_SNP_ID_7132834 A-to-I Human chr1 - 26878374 26878374 26878374 GGGAGGCTGAGGCAGAAGAATTGCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCCAAGATTGTG GGGAGGCTGAGGCAGAAGAATTGCTTGAACCCGGGAGGCGGAGGTTGCAGTGAGCCAAGATTGTG T C GPN2 Ensembl:ENSG00000142751 Protein coding 3'UTR GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1211594925 Functional Loss SNV dbSNP153 33..33 33 - - - 9587 RMVar_ID_9587 Human_SNP_ID_7132841 A-to-I Human chr1 - 26878422 26878422 26878422 TAAAAATTAGCTGGGCATGGTGTTGCACGCCTATAATCCCAGCTATTGGGGAGGCTGAGGCAGAA TAAAAATTAGCTGGGCATGGTGTTGCACGCCTGTAATCCCAGCTATTGGGGAGGCTGAGGCAGAA T C GPN2 Ensembl:ENSG00000142751 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560222313 Functional Loss SNV dbSNP153 33..33 33 - - - 9588 RMVar_ID_9588 Human_SNP_ID_7132956 A-to-I Human chr1 - 26878868 26878868 26878868 TTCAAGGCTGGGTGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGCGGA TTCAAGGCTGGGTGCGGTGGCTCACGCCTGTATTCCCAGCACTTTGGGAGGCCGAGGCAGGCGGA T A GPN2 Ensembl:ENSG00000142751 Protein coding 3'UTR GSE38233;GSE100210;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 24183664,29129909,30559470 RNA-Seq:(High) rs1367658677 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10906152 9589 RMVar_ID_9589 Human_SNP_ID_7133310 A-to-I Human chr1 - 26880495 26880495 26880495 CATTTCTGTCAACATGGTGAAACCCTGTCTCTACTAAAAATAGAAAAATTAGCTGGGTGTGCTGG CATTTCTGTCAACATGGTGAAACCCTGTCTCTGCTAAAAATAGAAAAATTAGCTGGGTGTGCTGG T C GPN2 Ensembl:ENSG00000142751 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1354896596 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98240,RMVar_hsa_circ_114927,RMVar_hsa_circ_117124,RMVar_hsa_circ_130700,RMVar_hsa_circ_130701,RMVar_hsa_circ_130702 9590 RMVar_ID_9590 Human_SNP_ID_7133345 A-to-I Human chr1 - 26880606 26880606 26880606 TTTTTTTAAAGTATAAAAATTTATTTTTGGCCAGGCGTGGTGGCTTACGCCTGTAATCCCAGCAC TTTTTTTAAAGTATAAAAATTTATTTTTGGCCGGGCGTGGTGGCTTACGCCTGTAATCCCAGCAC T C GPN2 Ensembl:ENSG00000142751 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1351982556 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98240,RMVar_hsa_circ_114927,RMVar_hsa_circ_117124,RMVar_hsa_circ_130700,RMVar_hsa_circ_130701,RMVar_hsa_circ_130702 9591 RMVar_ID_9591 Human_SNP_ID_7133658 A-to-I Human chr1 - 26882053 26882053 26882053 GCCACCACGCTCAGCTAATTTTTTGTATTTTTAGTAGAGACAGCGTTTTACCATGTTGGCCAGGC GCCACCACGCTCAGCTAATTTTTTGTATTTTTGGTAGAGACAGCGTTTTACCATGTTGGCCAGGC T C GPN2 Ensembl:ENSG00000142751 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs888862380 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98240,RMVar_hsa_circ_114927,RMVar_hsa_circ_117124,RMVar_hsa_circ_130700,RMVar_hsa_circ_130701,RMVar_hsa_circ_130702 9592 RMVar_ID_9592 Human_SNP_ID_7133691 A-to-I Human chr1 - 26882170 26882170 26882170 TCTTGTTGCCCCAGTTGGAGTGCAATGGTGCAATCTCAGCTCACTGCAACCTCCATCTCCCACGT TCTTGTTGCCCCAGTTGGAGTGCAATGGTGCAGTCTCAGCTCACTGCAACCTCCATCTCCCACGT T C GPN2 Ensembl:ENSG00000142751 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs552007333 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98240,RMVar_hsa_circ_114927,RMVar_hsa_circ_117124,RMVar_hsa_circ_130700,RMVar_hsa_circ_130701,RMVar_hsa_circ_130702 9593 RMVar_ID_9593 Human_SNP_ID_7133692 A-to-I Human chr1 - 26882178 26882178 26882178 ACCGTCAATCTTGTTGCCCCAGTTGGAGTGCAATGGTGCAATCTCAGCTCACTGCAACCTCCATC ACCGTCAATCTTGTTGCCCCAGTTGGAGTGCAGTGGTGCAATCTCAGCTCACTGCAACCTCCATC T C GPN2 Ensembl:ENSG00000142751 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs976566440 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98240,RMVar_hsa_circ_114927,RMVar_hsa_circ_117124,RMVar_hsa_circ_130700,RMVar_hsa_circ_130701,RMVar_hsa_circ_130702 9594 RMVar_ID_9594 Human_SNP_ID_7133761 A-to-I Human chr1 - 26882364 26882364 26882364 AAGAGGGGAGGAGCAATTTTTTTTTTAAATTTAAGATGGACTTTCTTTTGCTGTTGTTGCCCAGG AAGAGGGGAGGAGCAATTTTTTTTTTAAATTTCAGATGGACTTTCTTTTGCTGTTGTTGCCCAGG T G GPN2 Ensembl:ENSG00000142751 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs905677479 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5802965,Human_RBP_ID_10906320,Human_RBP_ID_17747429 RMVar_hsa_circ_98240,RMVar_hsa_circ_114927,RMVar_hsa_circ_117124,RMVar_hsa_circ_130700,RMVar_hsa_circ_130701,RMVar_hsa_circ_130702 9595 RMVar_ID_9595 Human_SNP_ID_7134063 A-to-I Human chr1 - 26883621 26883621 26883621 CACTGTGCCCAGTTAGTTTTTATATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGG CACTGTGCCCAGTTAGTTTTTATATTTTTAGTGGAGACGGGGTTTCACCATGTTGGCCAGGCTGG T C GPN2 Ensembl:ENSG00000142751 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs373540672 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98240,RMVar_hsa_circ_114927,RMVar_hsa_circ_117124,RMVar_hsa_circ_130700,RMVar_hsa_circ_130701,RMVar_hsa_circ_130702 9596 RMVar_ID_9596 Human_SNP_ID_7134067 A-to-I Human chr1 - 26883632 26883632 26883632 TTAGTGTGCGCCACTGTGCCCAGTTAGTTTTTATATTTTTAGTAGAGACGGGGTTTCACCATGTT TTAGTGTGCGCCACTGTGCCCAGTTAGTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTT T C GPN2 Ensembl:ENSG00000142751 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1429481767 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98240,RMVar_hsa_circ_114927,RMVar_hsa_circ_117124,RMVar_hsa_circ_130700,RMVar_hsa_circ_130701,RMVar_hsa_circ_130702 9597 RMVar_ID_9597 Human_SNP_ID_7134086 A-to-I Human chr1 - 26883697 26883697 26883697 TCTGTGTAACCTCTGCCTCCCATATTCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGTA TCTGTGTAACCTCTGCCTCCCATATTCAAGCAGTTCTCCTGCCTCAGCCTCCCAAGTAGCTGGTA T C GPN2 Ensembl:ENSG00000142751 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs993559638 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98240,RMVar_hsa_circ_114927,RMVar_hsa_circ_117124,RMVar_hsa_circ_130700,RMVar_hsa_circ_130701,RMVar_hsa_circ_130702 9598 RMVar_ID_9598 Human_SNP_ID_7134090 A-to-I Human chr1 - 26883721 26883721 26883721 ATCGCACAATGGCGCAATCTTGGCTCTGTGTAACCTCTGCCTCCCATATTCAAGCAATTCTCCTG ATCGCACAATGGCGCAATCTTGGCTCTGTGTATCCTCTGCCTCCCATATTCAAGCAATTCTCCTG T A GPN2 Ensembl:ENSG00000142751 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1166364073 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10906384 RMVar_hsa_circ_98240,RMVar_hsa_circ_114927,RMVar_hsa_circ_117124,RMVar_hsa_circ_130700,RMVar_hsa_circ_130701,RMVar_hsa_circ_130702 9599 RMVar_ID_9599 Human_SNP_ID_7134092 A-to-I Human chr1 - 26883737 26883737 26883737 TTGTTGCCCAGGCTGGATCGCACAATGGCGCAATCTTGGCTCTGTGTAACCTCTGCCTCCCATAT TTGTTGCCCAGGCTGGATCGCACAATGGCGCATTCTTGGCTCTGTGTAACCTCTGCCTCCCATAT T A GPN2 Ensembl:ENSG00000142751 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs529560500 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10906384 RMVar_hsa_circ_98240,RMVar_hsa_circ_114927,RMVar_hsa_circ_117124,RMVar_hsa_circ_130700,RMVar_hsa_circ_130701,RMVar_hsa_circ_130702 9600 RMVar_ID_9600 Human_SNP_ID_7134093 A-to-I Human chr1 - 26883737 26883737 26883737 TTGTTGCCCAGGCTGGATCGCACAATGGCGCAATCTTGGCTCTGTGTAACCTCTGCCTCCCATAT TTGTTGCCCAGGCTGGATCGCACAATGGCGCAGTCTTGGCTCTGTGTAACCTCTGCCTCCCATAT T C GPN2 Ensembl:ENSG00000142751 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs529560500 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10906384 RMVar_hsa_circ_98240,RMVar_hsa_circ_114927,RMVar_hsa_circ_117124,RMVar_hsa_circ_130700,RMVar_hsa_circ_130701,RMVar_hsa_circ_130702 9601 RMVar_ID_9601 Human_SNP_ID_7134094 A-to-I Human chr1 - 26883738 26883738 26883738 CTTGTTGCCCAGGCTGGATCGCACAATGGCGCAATCTTGGCTCTGTGTAACCTCTGCCTCCCATA CTTGTTGCCCAGGCTGGATCGCACAATGGCGCCATCTTGGCTCTGTGTAACCTCTGCCTCCCATA T G GPN2 Ensembl:ENSG00000142751 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350692136 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10906384 RMVar_hsa_circ_98240,RMVar_hsa_circ_114927,RMVar_hsa_circ_117124,RMVar_hsa_circ_130700,RMVar_hsa_circ_130701,RMVar_hsa_circ_130702 9602 RMVar_ID_9602 Human_SNP_ID_7134901 A-to-I Human chr1 - 26886568 26886568 26886568 GTGATCCGTCCATCTCCCAAAGTGCTGGGATTACAGGCTTGAGCCACCGCACCTGGCCTAATTTT GTGATCCGTCCATCTCCCAAAGTGCTGGGATTGCAGGCTTGAGCCACCGCACCTGGCCTAATTTT T C GPN2 Ensembl:ENSG00000142751 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1267714376 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_35419 RMVar_hsa_circ_98240,RMVar_hsa_circ_114927,RMVar_hsa_circ_130701,RMVar_hsa_circ_130702 9603 RMVar_ID_9603 Human_SNP_ID_7146254 A-to-I Human chr1 + 26927598 26927598 26927598 TTTCGTATTTTTAGTAGAGCCGGGGTTTCACCATGTTGGTCAGGTTGGTCTCGAACTCCTGAGCT TTTCGTATTTTTAGTAGAGCCGGGGTTTCACCGTGTTGGTCAGGTTGGTCTCGAACTCCTGAGCT A G NUDC Ensembl:ENSG00000090273 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1001003715 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10906680 RMVar_hsa_circ_72978,RMVar_hsa_circ_78830,RMVar_hsa_circ_127588,RMVar_hsa_circ_130706,RMVar_hsa_circ_130707,RMVar_hsa_circ_79261,RMVar_hsa_circ_130708 9604 RMVar_ID_9604 Human_SNP_ID_7147134 A-to-I Human chr1 + 26931133 26931133 26931133 GGAGTCTCGCTCTGTTGCCCAGCCTGGAGTGCAGTGGCGCCATCTTGGCTCACTGCAACCTCTGC GGAGTCTCGCTCTGTTGCCCAGCCTGGAGTGCGGTGGCGCCATCTTGGCTCACTGCAACCTCTGC A G NUDC Ensembl:ENSG00000090273 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1056723115 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72978,RMVar_hsa_circ_78830,RMVar_hsa_circ_127588,RMVar_hsa_circ_130706,RMVar_hsa_circ_130707,RMVar_hsa_circ_79261,RMVar_hsa_circ_130708 9605 RMVar_ID_9605 Human_SNP_ID_7147165 A-to-I Human chr1 + 26931195 26931195 26931195 TGCCTCCCAGGTTCCAGCAGTTCTCCCACCTCAGCCTCCCGAGTAGCTGGGATTACAGGCGTGTG TGCCTCCCAGGTTCCAGCAGTTCTCCCACCTCCGCCTCCCGAGTAGCTGGGATTACAGGCGTGTG A C NUDC Ensembl:ENSG00000090273 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1489553927 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72978,RMVar_hsa_circ_78830,RMVar_hsa_circ_127588,RMVar_hsa_circ_130706,RMVar_hsa_circ_130707,RMVar_hsa_circ_79261,RMVar_hsa_circ_130708 9606 RMVar_ID_9606 Human_SNP_ID_7147900 A-to-I Human chr1 + 26933871 26933871 26933871 CAGACTGGGTAATTCATAAAGAAAAGAGGATTACGGCTGGGCACGGTGGCTCACGCCTGTAATCC CAGACTGGGTAATTCATAAAGAAAAGAGGATTGCGGCTGGGCACGGTGGCTCACGCCTGTAATCC A G NUDC Ensembl:ENSG00000090273 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs541225248 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72978,RMVar_hsa_circ_78830,RMVar_hsa_circ_127588,RMVar_hsa_circ_130706,RMVar_hsa_circ_130707,RMVar_hsa_circ_79261,RMVar_hsa_circ_130708 9607 RMVar_ID_9607 Human_SNP_ID_7147956 A-to-I Human chr1 + 26933969 26933969 26933969 GAGGTCAGGAGATCAAGAACATCCTGGCCAACATGGTGAAACCCCAGCTCTCCTAAAAATACAAA GAGGTCAGGAGATCAAGAACATCCTGGCCAACGTGGTGAAACCCCAGCTCTCCTAAAAATACAAA A G NUDC Ensembl:ENSG00000090273 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1033316331 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72978,RMVar_hsa_circ_78830,RMVar_hsa_circ_127588,RMVar_hsa_circ_130706,RMVar_hsa_circ_130707,RMVar_hsa_circ_79261,RMVar_hsa_circ_130708 9608 RMVar_ID_9608 Human_SNP_ID_7148399 A-to-I Human chr1 + 26935345 26935345 26935345 TCTAGGGTATTCCTTCATAGCAGCATGAGAACAGACTAATACAGAACCCTCATGTACTATGGCCA TCTAGGGTATTCCTTCATAGCAGCATGAGAACGGACTAATACAGAACCCTCATGTACTATGGCCA A G NUDC Ensembl:ENSG00000090273 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1297991607 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72978,RMVar_hsa_circ_78830,RMVar_hsa_circ_127588,RMVar_hsa_circ_130706,RMVar_hsa_circ_130707,RMVar_hsa_circ_79261,RMVar_hsa_circ_130708 9609 RMVar_ID_9609 Human_SNP_ID_7150555 A-to-I Human chr1 + 26943266 26943266 26943266 GTCTCACTCTGTTGCCCAGGCTGAAGTGCAGTAACACCTTCTTAGCTCACTGCAGCCTTGAACCC GTCTCACTCTGTTGCCCAGGCTGAAGTGCAGTCACACCTTCTTAGCTCACTGCAGCCTTGAACCC A C NUDC Ensembl:ENSG00000090273 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs79056567 Functional Loss SNV dbSNP153 33..33 33 - - - 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_130714,RMVar_hsa_circ_83021,RMVar_hsa_circ_130715 9610 RMVar_ID_9610 Human_SNP_ID_7150612 A-to-I Human chr1 + 26943427 26943427 26943427 TGTAGAGACCGGGGGGTCTCACTATATTTCCCAGGCTGGTCTTGAACTCCTGGCCTCAAGTGATC TGTAGAGACCGGGGGGTCTCACTATATTTCCCGGGCTGGTCTTGAACTCCTGGCCTCAAGTGATC A G NUDC Ensembl:ENSG00000090273 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1421475381 Functional Loss SNV dbSNP153 33..33 33 - - - 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_130714,RMVar_hsa_circ_83021,RMVar_hsa_circ_130715 9611 RMVar_ID_9611 Human_SNP_ID_7150773 A-to-I Human chr1 + 26944085 26944084 26944086 GTCTGTTTTGTTTTCTATTTTTTAGTAGAGACAGGGTTTCACCGTGTTAGCCAGGATGGTCTCGA GTCTGTTTTGTTTTCTATTTTTTAGTAGAGAC__GGTTTCACCGTGTTAGCCAGGATGGTCTCGA CAG C NUDC Ensembl:ENSG00000090273 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1357279575 Functional Loss DEL dbSNP153 33..34 33 - - - 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_130714,RMVar_hsa_circ_83021,RMVar_hsa_circ_130715 9612 RMVar_ID_9612 Human_SNP_ID_7150774 A-to-I Human chr1 + 26944085 26944085 26944085 GTCTGTTTTGTTTTCTATTTTTTAGTAGAGACAGGGTTTCACCGTGTTAGCCAGGATGGTCTCGA GTCTGTTTTGTTTTCTATTTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGGTCTCGA A G NUDC Ensembl:ENSG00000090273 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs976895824 Functional Loss SNV dbSNP153 33..33 33 - - - 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_130714,RMVar_hsa_circ_83021,RMVar_hsa_circ_130715 9613 RMVar_ID_9613 Human_SNP_ID_7150792 A-to-I Human chr1 + 26944177 26944138 26944178 CGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCATGCCCAGCCCTTTCCCTGCCTTTTA __________________________________CCACCATGCCCAGCCCTTTCCCTGCCTTTTA CCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG C NUDC Ensembl:ENSG00000090273 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1313129861 Functional Loss DEL dbSNP153 1..34 33 - - - 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_130714,RMVar_hsa_circ_83021,RMVar_hsa_circ_130715 9614 RMVar_ID_9614 Human_SNP_ID_7150815 A-to-I Human chr1 + 26944234 26944234 26944234 GCCTTTTAAATTTATTTTTTATTTTTTGAGACAGGGTCTTGTTCTCACCCAGGCTGGAATGCAGT GCCTTTTAAATTTATTTTTTATTTTTTGAGACGGGGTCTTGTTCTCACCCAGGCTGGAATGCAGT A G NUDC Ensembl:ENSG00000090273 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1433050221 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11206552,Human_RBP_ID_23148168 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_130714,RMVar_hsa_circ_83021,RMVar_hsa_circ_130715 9615 RMVar_ID_9615 Human_SNP_ID_7150897 A-to-I Human chr1 + 26944535 26944535 26944535 CTGCTTAAAAACTTTTTCTGGCTGGGCGTGGTAGCTCATGCCTGTAATCCTAGCGCTTTGGGAGG CTGCTTAAAAACTTTTTCTGGCTGGGCGTGGTTGCTCATGCCTGTAATCCTAGCGCTTTGGGAGG A T NUDC Ensembl:ENSG00000090273 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1378398651 Functional Loss SNV dbSNP153 33..33 33 - - - 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_130714,RMVar_hsa_circ_83021,RMVar_hsa_circ_130715 9616 RMVar_ID_9616 Human_SNP_ID_7150942 A-to-I Human chr1 + 26944727 26944727 26944727 GGGAGTCTGAGGCAGGAGAATCGCTTGAACCCAGGAGGTGGAGGTTGCAGTGAGCTGACTGCACC GGGAGTCTGAGGCAGGAGAATCGCTTGAACCCGGGAGGTGGAGGTTGCAGTGAGCTGACTGCACC A G NUDC Ensembl:ENSG00000090273 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs925577622 Functional Loss SNV dbSNP153 33..33 33 - - - 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_130714,RMVar_hsa_circ_83021,RMVar_hsa_circ_130715 9617 RMVar_ID_9617 Human_SNP_ID_7163606 A-to-I Human chr1 + 26995760 26995760 26995760 TCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCATGTGCCACTATGCCCA TCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTGGCTGGGATTACAGGCATGTGCCACTATGCCCA A G TRNP1 Ensembl:ENSG00000253368 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1390722271 Functional Loss SNV dbSNP153 33..33 33 - - - 9618 RMVar_ID_9618 Human_SNP_ID_7198964 A-to-I Human chr1 - 27131902 27131902 27131902 TTCTTCTTCTTTTTGAGACGGATTCTCCCTCTATTGCCCAGGCTAGAATGCAGTGGTGCCGTCTA TTCTTCTTCTTTTTGAGACGGATTCTCCCTCTGTTGCCCAGGCTAGAATGCAGTGGTGCCGTCTA T C SLC9A1 Ensembl:ENSG00000090020 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1457387054 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269034 9619 RMVar_ID_9619 Human_SNP_ID_7201992 A-to-I Human chr1 - 27144843 27144842 27144844 ACCACGCCCAGCTAATTTTTTGTGTTTTTAGTAGAGACGGGGTTTTGCTATGCTGGCCAGTCTGG ACCACGCCCAGCTAATTTTTTGTGTTTTTAG__GAGACGGGGTTTTGCTATGCTGGCCAGTCTGG CTA C SLC9A1 Ensembl:ENSG00000090020 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs56878944 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_269034 9620 RMVar_ID_9620 Human_SNP_ID_7217529 A-to-I Human chr1 + 27207086 27207086 27207086 TATCTTTAAGAACGGTCAGTTTAGGGGCTGGTACAAAGGATGAATTGCACATTGTTGAAGCAGAG TATCTTTAAGAACGGTCAGTTTAGGGGCTGGTGCAAAGGATGAATTGCACATTGTTGAAGCAGAG A G NPM1P39 Ensembl:ENSG00000225159 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878959994 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5160393 9621 RMVar_ID_9621 Human_SNP_ID_7246024 A-to-I Human chr1 + 27325712 27325712 27325712 TCTGTGTGGATCAGCGGCTCCATCCTGGCCTCACTGTCCACCTTCCAGCAGATGTGGATTAGCAA TCTGTGTGGATCAGCGGCTCCATCCTGGCCTCGCTGTCCACCTTCCAGCAGATGTGGATTAGCAA A G ACTG1P20,TMEM222 Ensembl:ENSG00000241547,Ensembl:ENSG00000186501 Pseudogene,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1557521657 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_350500 RMVar_hsa_circ_106748,RMVar_hsa_circ_130737 9622 RMVar_ID_9622 Human_SNP_ID_7246218 A-to-I Human chr1 - 27326519 27326511 27326519 TAGTTTCTTTTTTTTCCCTTTTTTTTGGTTACAGCAGCACTTTTATTTTTCCTTACACAATGACA TAGTTTCTTTTTTTTCCCTTTTTTTTGGTTAC________TTTTATTTTTCCTTACACAATGACA AGTGCTGCT A - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1406031615 Functional Loss DEL dbSNP153 33..40 33 - - - 9623 RMVar_ID_9623 Human_SNP_ID_7250783 A-to-I Human chr1 + 27344203 27344203 27344203 TCGGTTTACCATAACCTCTGCCTCCCAGTTTCAAGCAATTCTCCCACCTCAGCCTCCCGAGTAGC TCGGTTTACCATAACCTCTGCCTCCCAGTTTCGAGCAATTCTCCCACCTCAGCCTCCCGAGTAGC A G SYTL1 Ensembl:ENSG00000142765 Protein coding intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1291344764 Functional Loss SNV dbSNP153 33..33 33 - - - 9624 RMVar_ID_9624 Human_SNP_ID_7250806 A-to-I Human chr1 + 27344323 27344323 27344323 CGGGGTTTCTCCGTGTTGGTCAGGCTGGTCTCAAACTCCTGACCTCAGGTGATCTGCCCGCCTTG CGGGGTTTCTCCGTGTTGGTCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCTGCCCGCCTTG A G SYTL1 Ensembl:ENSG00000142765 Protein coding intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1034230413 Functional Loss SNV dbSNP153 33..33 33 - - - 9625 RMVar_ID_9625 Human_SNP_ID_7268854 A-to-I Human chr1 - 27407274 27407274 27407274 CTGAGGCCTAGAGATGGGAAGTGACTTGCTCAAGGTCACACAATTGGATAGTGACATAGCTAGAG CTGAGGCCTAGAGATGGGAAGTGACTTGCTCAGGGTCACACAATTGGATAGTGACATAGCTAGAG T C WASF2 Ensembl:ENSG00000158195 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1209573230 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_467447,Human_miRNA_ID_605605 9626 RMVar_ID_9626 Human_SNP_ID_7269975 A-to-I Human chr1 - 27411824 27411824 27411824 GAGTCTCACTCTGTCACCCAGGCTGGAGTGCAATGGCGCGATCTTGGCTAACTGCAAGCTCCGCC GAGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGCGCGATCTTGGCTAACTGCAAGCTCCGCC T C WASF2 Ensembl:ENSG00000158195 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1214846878 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17371 9627 RMVar_ID_9627 Human_SNP_ID_7270097 A-to-I Human chr1 - 27412407 27412407 27412407 GGCCAAAAGTTCAAGACCAGTCTGGGTAACATAGCAAGACTTCATCCCTACTAAAAATCAAAAAA GGCCAAAAGTTCAAGACCAGTCTGGGTAACATGGCAAGACTTCATCCCTACTAAAAATCAAAAAA T C WASF2 Ensembl:ENSG00000158195 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1239644723 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17371 9628 RMVar_ID_9628 Human_SNP_ID_7275221 A-to-I Human chr1 - 27435111 27435111 27435111 GAAACCCCATCTCTACTAAAAATACAAAAATTAGTGGGCATGGTGCTGTATGCCTGTAATCCCAG GAAACCCCATCTCTACTAAAAATACAAAAATTCGTGGGCATGGTGCTGTATGCCTGTAATCCCAG T G WASF2 Ensembl:ENSG00000158195 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs951760301 Functional Loss SNV dbSNP153 33..33 33 - - - 9629 RMVar_ID_9629 Human_SNP_ID_7279624 A-to-I Human chr1 - 27453529 27453529 27453529 GGAGTGCAGTGGAGTGATCTCCACTCACGGCAACCTCTGCCTCCTGGGTTCAAGAAATTCTCCTG GGAGTGCAGTGGAGTGATCTCCACTCACGGCATCCTCTGCCTCCTGGGTTCAAGAAATTCTCCTG T A WASF2 Ensembl:ENSG00000158195 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1400457598 Functional Loss SNV dbSNP153 33..33 33 - - - 9630 RMVar_ID_9630 Human_SNP_ID_7279625 A-to-I Human chr1 - 27453529 27453529 27453529 GGAGTGCAGTGGAGTGATCTCCACTCACGGCAACCTCTGCCTCCTGGGTTCAAGAAATTCTCCTG GGAGTGCAGTGGAGTGATCTCCACTCACGGCACCCTCTGCCTCCTGGGTTCAAGAAATTCTCCTG T G WASF2 Ensembl:ENSG00000158195 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1400457598 Functional Loss SNV dbSNP153 33..33 33 - - - 9631 RMVar_ID_9631 Human_SNP_ID_7280723 A-to-I Human chr1 - 27456919 27456919 27456919 TGGCCAACATGACAAAACACCATCTCTACTAAAAATACAAAAAAAATTGCCGGGCGTGGCGGCGG TGGCCAACATGACAAAACACCATCTCTACTAACAATACAAAAAAAATTGCCGGGCGTGGCGGCGG T G WASF2 Ensembl:ENSG00000158195 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs758167452 Functional Loss SNV dbSNP153 33..33 33 - - - 9632 RMVar_ID_9632 Human_SNP_ID_7280927 A-to-I Human chr1 - 27457759 27457759 27457759 AAAATTAGCCAGGAGAGGTAGCTCACACCTATAGTCTTAACTACTCAGGAGGCTGAGGCAAGAGG AAAATTAGCCAGGAGAGGTAGCTCACACCTATGGTCTTAACTACTCAGGAGGCTGAGGCAAGAGG T C WASF2 Ensembl:ENSG00000158195 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1349748539 Functional Loss SNV dbSNP153 33..33 33 - - - 9633 RMVar_ID_9633 Human_SNP_ID_7282590 A-to-I Human chr1 - 27464259 27464259 27464259 CTCCTGCCTTAGCCTCCTGAATAGCTGGGATTACAGGCACCCACCACCATGCCCAGCTAATTTTT CTCCTGCCTTAGCCTCCTGAATAGCTGGGATTGCAGGCACCCACCACCATGCCCAGCTAATTTTT T C WASF2 Ensembl:ENSG00000158195 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1319797724 Functional Loss SNV dbSNP153 33..33 33 - - - 9634 RMVar_ID_9634 Human_SNP_ID_7282607 A-to-I Human chr1 - 27464355 27464355 27464355 TTTTGAGACCGTTTTCCTCTTTTGCCCAGGCTAGAGTGCAATGGTGTGATCTTGGCTCACTGTAA TTTTGAGACCGTTTTCCTCTTTTGCCCAGGCTGGAGTGCAATGGTGTGATCTTGGCTCACTGTAA T C WASF2 Ensembl:ENSG00000158195 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1330671541 Functional Loss SNV dbSNP153 33..33 33 - - - 9635 RMVar_ID_9635 Human_SNP_ID_7285440 A-to-I Human chr1 - 27475703 27475703 27475703 GGATCACTTGAACCCAGGAGGCAGAGGTTGCAATGAGCCAAGATTATGCCACTGCACTCCAGCCT GGATCACTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCCAAGATTATGCCACTGCACTCCAGCCT T C WASF2 Ensembl:ENSG00000158195 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs904521299 Functional Loss SNV dbSNP153 33..33 33 - - - 9636 RMVar_ID_9636 Human_SNP_ID_7287853 A-to-I Human chr1 - 27485067 27485067 27485067 TGGCTCACTGCTACCTCTGCCTCCTGGGTTCAAACAATTCTCCTGCCTCAGCCTCCTGAGTAGCT TGGCTCACTGCTACCTCTGCCTCCTGGGTTCAGACAATTCTCCTGCCTCAGCCTCCTGAGTAGCT T C WASF2 Ensembl:ENSG00000158195 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1002568645 Functional Loss SNV dbSNP153 33..33 33 - - - 9637 RMVar_ID_9637 Human_SNP_ID_7288235 A-to-I Human chr1 - 27486667 27486664 27486667 CACCTGCTGCGGCCTCCGGAAGTGCTGGGATTACAGGCGTGAGCCACCACGCCCAGCTGAGTCTT CACCTGCTGCGGCCTCCGGAAGTGCTGGGATT___GGCGTGAGCCACCACGCCCAGCTGAGTCTT CTGT C WASF2 Ensembl:ENSG00000158195 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1286177035 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_22707960,Human_RBP_ID_24677871 9638 RMVar_ID_9638 Human_SNP_ID_7288238 A-to-I Human chr1 - 27486667 27486667 27486667 CACCTGCTGCGGCCTCCGGAAGTGCTGGGATTACAGGCGTGAGCCACCACGCCCAGCTGAGTCTT CACCTGCTGCGGCCTCCGGAAGTGCTGGGATTCCAGGCGTGAGCCACCACGCCCAGCTGAGTCTT T G WASF2 Ensembl:ENSG00000158195 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1214934375 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22707960,Human_RBP_ID_24677871 9639 RMVar_ID_9639 Human_SNP_ID_7334716 A-to-I Human chr1 - 27666203 27666203 27666203 GCGAACATAGTACACTGCAGCCTCCAACTCCTAGCCTCAAGTGATCCTCCTGTCTCAACCTCCCA GCGAACATAGTACACTGCAGCCTCCAACTCCTGGCCTCAAGTGATCCTCCTGTCTCAACCTCCCA T C IFI6 Ensembl:ENSG00000126709 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037628691 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_350643,Human_RBP_ID_10908670 Human_miRNA_ID_1393420 RMVar_hsa_circ_76645,RMVar_hsa_circ_110208,RMVar_hsa_circ_123731,RMVar_hsa_circ_119380,RMVar_hsa_circ_85756,RMVar_hsa_circ_130750,RMVar_hsa_circ_130752,RMVar_hsa_circ_130753,RMVar_hsa_circ_130754,RMVar_hsa_circ_130751 9640 RMVar_ID_9640 Human_SNP_ID_7334717 A-to-I Human chr1 - 27666203 27666203 27666203 GCGAACATAGTACACTGCAGCCTCCAACTCCTAGCCTCAAGTGATCCTCCTGTCTCAACCTCCCA GCGAACATAGTACACTGCAGCCTCCAACTCCTCGCCTCAAGTGATCCTCCTGTCTCAACCTCCCA T G IFI6 Ensembl:ENSG00000126709 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037628691 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_350643,Human_RBP_ID_10908670 Human_miRNA_ID_1393420 RMVar_hsa_circ_76645,RMVar_hsa_circ_110208,RMVar_hsa_circ_123731,RMVar_hsa_circ_119380,RMVar_hsa_circ_85756,RMVar_hsa_circ_130750,RMVar_hsa_circ_130752,RMVar_hsa_circ_130753,RMVar_hsa_circ_130754,RMVar_hsa_circ_130751 9641 RMVar_ID_9641 Human_SNP_ID_7334719 A-to-I Human chr1 - 27666209 27666209 27666209 ACAGATGCGAACATAGTACACTGCAGCCTCCAACTCCTAGCCTCAAGTGATCCTCCTGTCTCAAC ACAGATGCGAACATAGTACACTGCAGCCTCCATCTCCTAGCCTCAAGTGATCCTCCTGTCTCAAC T A IFI6 Ensembl:ENSG00000126709 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs532903043 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_350643,Human_RBP_ID_10908670 RMVar_hsa_circ_76645,RMVar_hsa_circ_110208,RMVar_hsa_circ_123731,RMVar_hsa_circ_119380,RMVar_hsa_circ_85756,RMVar_hsa_circ_130750,RMVar_hsa_circ_130752,RMVar_hsa_circ_130753,RMVar_hsa_circ_130754,RMVar_hsa_circ_130751 9642 RMVar_ID_9642 Human_SNP_ID_7356131 A-to-I Human chr1 + 27756936 27756936 27756936 CAAAAATTAGCAGGGCTTGATGGTGTGCACCTATGGTCCCAGCTACTTGGGAGGCTAAGGTGGGA CAAAAATTAGCAGGGCTTGATGGTGTGCACCTGTGGTCCCAGCTACTTGGGAGGCTAAGGTGGGA A G FAM76A Ensembl:ENSG00000009780 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1234104237 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_130759,RMVar_hsa_circ_100521,RMVar_hsa_circ_357884,RMVar_hsa_circ_313533 9643 RMVar_ID_9643 Human_SNP_ID_7356140 A-to-I Human chr1 + 27756974 27756974 27756974 CCAGCTACTTGGGAGGCTAAGGTGGGAGGATCACCTTAGCCTGGGAGGTCAAGGCTGTGGTGAGC CCAGCTACTTGGGAGGCTAAGGTGGGAGGATCCCCTTAGCCTGGGAGGTCAAGGCTGTGGTGAGC A C FAM76A Ensembl:ENSG00000009780 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1194694811 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_130759,RMVar_hsa_circ_100521,RMVar_hsa_circ_357884,RMVar_hsa_circ_313533 9644 RMVar_ID_9644 Human_SNP_ID_7366651 A-to-I Human chr1 + 27800784 27800784 27800784 CAAGTGATCCTCCTGCCTCAGCCTCCCAAAATACTAGGACTATAGGCATAAGCCACTGTGCTCAA CAAGTGATCCTCCTGCCTCAGCCTCCCAAAATGCTAGGACTATAGGCATAAGCCACTGTGCTCAA A G STX12 Ensembl:ENSG00000117758 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs932473419 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_273478,RMVar_hsa_circ_288719,RMVar_hsa_circ_330900,RMVar_hsa_circ_130765,RMVar_hsa_circ_130766,RMVar_hsa_circ_130764,RMVar_hsa_circ_130768,RMVar_hsa_circ_84152,RMVar_hsa_circ_345469,RMVar_hsa_circ_355890,RMVar_hsa_circ_130769 9645 RMVar_ID_9645 Human_SNP_ID_7368355 A-to-I Human chr1 + 27808445 27808445 27808445 CTCACTGCAACCTCTGCCTTCTAGGTTCAAGCAATTCTCCTGCCTTAGCCTCTCGAGTAGCTGGG CTCACTGCAACCTCTGCCTTCTAGGTTCAAGCGATTCTCCTGCCTTAGCCTCTCGAGTAGCTGGG A G STX12 Ensembl:ENSG00000117758 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs978285785 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_273478,RMVar_hsa_circ_330900,RMVar_hsa_circ_130765,RMVar_hsa_circ_130766,RMVar_hsa_circ_345469,RMVar_hsa_circ_355890,RMVar_hsa_circ_130769,RMVar_hsa_circ_363164 9646 RMVar_ID_9646 Human_SNP_ID_7375366 A-to-I Human chr1 + 27836776 27836776 27836776 AGCTCAGGTCTAGCACGGTGGCTAACACCGGTAATCCCAGCACTTTGGGAGGTTGAGGCTGGCCA AGCTCAGGTCTAGCACGGTGGCTAACACCGGTTATCCCAGCACTTTGGGAGGTTGAGGCTGGCCA A T PPP1R8 Ensembl:ENSG00000117751 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1361066096 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94793,RMVar_hsa_circ_130771 9647 RMVar_ID_9647 Human_SNP_ID_7377042 A-to-I Human chr1 + 27843561 27843561 27843561 GTTCGCCTGTAGTCCCAGCTACTTGGGAGGTTAAGGCAGGAGAATTGCTTGAACCCAGGAGGCAG GTTCGCCTGTAGTCCCAGCTACTTGGGAGGTTGAGGCAGGAGAATTGCTTGAACCCAGGAGGCAG A G PPP1R8 Ensembl:ENSG00000117751 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1450173692 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8194,RMVar_hsa_circ_282276,RMVar_hsa_circ_130773 9648 RMVar_ID_9648 Human_SNP_ID_7377181 A-to-I Human chr1 + 27844080 27844080 27844080 GCTAGAGTGCAGTGGCACAGTCACGGCTCACTACAGCCTTGACCACCCAGGCTCAGGTGATCCTC GCTAGAGTGCAGTGGCACAGTCACGGCTCACTGCAGCCTTGACCACCCAGGCTCAGGTGATCCTC A G PPP1R8 Ensembl:ENSG00000117751 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs905563526 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8194,RMVar_hsa_circ_282276,RMVar_hsa_circ_130773 9649 RMVar_ID_9649 Human_SNP_ID_7377298 A-to-I Human chr1 + 27844595 27844595 27844595 CAGGTGATCTGCCCTCAACCTCCCAAAGTGCTAGGATTACAGGCGTGAGCTACCGCGCCCAGCCC CAGGTGATCTGCCCTCAACCTCCCAAAGTGCTGGGATTACAGGCGTGAGCTACCGCGCCCAGCCC A G PPP1R8 Ensembl:ENSG00000117751 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1200662093 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8194,RMVar_hsa_circ_282276,RMVar_hsa_circ_130773 9650 RMVar_ID_9650 Human_SNP_ID_7378719 A-to-I Human chr1 + 27849558 27849558 27849558 TTACTCTGTCACCCAGGCTGCAGTGCAGTGGCACCATCTCAGCTCATTGCAAACTCTGCCTCAAG TTACTCTGTCACCCAGGCTGCAGTGCAGTGGCGCCATCTCAGCTCATTGCAAACTCTGCCTCAAG A G PPP1R8 Ensembl:ENSG00000117751 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1408849320 Functional Loss SNV dbSNP153 33..33 33 - - - 9651 RMVar_ID_9651 Human_SNP_ID_7378733 A-to-I Human chr1 + 27849618 27849618 27849618 TCAAGTGATTCTTGTGCCTCAGCCTCCCGAGTAGCTGTGATTACAGGCACCTGCCACCACGCCTG TCAAGTGATTCTTGTGCCTCAGCCTCCCGAGTGGCTGTGATTACAGGCACCTGCCACCACGCCTG A G PPP1R8 Ensembl:ENSG00000117751 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1311692137 Functional Loss SNV dbSNP153 33..33 33 - - - 9652 RMVar_ID_9652 Human_SNP_ID_7378736 A-to-I Human chr1 + 27849628 27849628 27849628 CTTGTGCCTCAGCCTCCCGAGTAGCTGTGATTACAGGCACCTGCCACCACGCCTGGCTAATTTTT CTTGTGCCTCAGCCTCCCGAGTAGCTGTGATTTCAGGCACCTGCCACCACGCCTGGCTAATTTTT A T PPP1R8 Ensembl:ENSG00000117751 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs535305355 Functional Loss SNV dbSNP153 33..33 33 - - - 9653 RMVar_ID_9653 Human_SNP_ID_7387244 A-to-I Human chr1 + 27880447 27880447 27880447 ACCTCAGGTGGTCCACCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGTTC ACCTCAGGTGGTCCACCCGCCTTGGCCTCCCACAGTGCTGGGATTACAGGCGTGAGCCACCGTTC A C THEMIS2 Ensembl:ENSG00000130775 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs960759323 Functional Loss SNV dbSNP153 33..33 33 - - - 9654 RMVar_ID_9654 Human_SNP_ID_7387245 A-to-I Human chr1 + 27880447 27880447 27880447 ACCTCAGGTGGTCCACCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGTTC ACCTCAGGTGGTCCACCCGCCTTGGCCTCCCATAGTGCTGGGATTACAGGCGTGAGCCACCGTTC A T THEMIS2 Ensembl:ENSG00000130775 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs960759323 Functional Loss SNV dbSNP153 33..33 33 - - - 9655 RMVar_ID_9655 Human_SNP_ID_7391918 A-to-I Human chr1 - 27898686 27898686 27898686 AAAAAATTAACCAGGTGTGGTGGCAGGCGCCTATAGTCCCAGCTATTTGGGAGGCTGAGGCAGGA AAAAAATTAACCAGGTGTGGTGGCAGGCGCCTGTAGTCCCAGCTATTTGGGAGGCTGAGGCAGGA T C RPA2 Ensembl:ENSG00000117748 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs187547321 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117034,RMVar_hsa_circ_91680,RMVar_hsa_circ_96066,RMVar_hsa_circ_130779,RMVar_hsa_circ_130781,RMVar_hsa_circ_130780,RMVar_hsa_circ_8731,RMVar_hsa_circ_366405,RMVar_hsa_circ_130784,RMVar_hsa_circ_298937,RMVar_hsa_circ_130786 9656 RMVar_ID_9656 Human_SNP_ID_7391946 A-to-I Human chr1 - 27898763 27898763 27898763 CATGAGGTCAGGAGATCGAGACCATCCTGGCCAACATGGGGAAACCCCGTCTCTACTAAAGATAC CATGAGGTCAGGAGATCGAGACCATCCTGGCCGACATGGGGAAACCCCGTCTCTACTAAAGATAC T C RPA2 Ensembl:ENSG00000117748 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs944686140 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117034,RMVar_hsa_circ_91680,RMVar_hsa_circ_96066,RMVar_hsa_circ_130779,RMVar_hsa_circ_130781,RMVar_hsa_circ_130780,RMVar_hsa_circ_8731,RMVar_hsa_circ_366405,RMVar_hsa_circ_130784,RMVar_hsa_circ_298937,RMVar_hsa_circ_130786 9657 RMVar_ID_9657 Human_SNP_ID_7392015 A-to-I Human chr1 - 27899042 27899042 27899042 AGCATATATTTTCTAGTTTTTTGTTTGTTTTTAGAGACGAGGTCTCACTATGTTGCCCAGGCTGG AGCATATATTTTCTAGTTTTTTGTTTGTTTTTGGAGACGAGGTCTCACTATGTTGCCCAGGCTGG T C RPA2 Ensembl:ENSG00000117748 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs891966901 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117034,RMVar_hsa_circ_91680,RMVar_hsa_circ_96066,RMVar_hsa_circ_130779,RMVar_hsa_circ_130781,RMVar_hsa_circ_130780,RMVar_hsa_circ_8731,RMVar_hsa_circ_366405,RMVar_hsa_circ_130784,RMVar_hsa_circ_298937,RMVar_hsa_circ_130786 9658 RMVar_ID_9658 Human_SNP_ID_7392029 A-to-I Human chr1 - 27899122 27899122 27899122 GTGACTTGCTCGCCTTGGCCTCCCAAAATGCTAGGATTACAGGCATGAGTCACTGCACCTGGCCA GTGACTTGCTCGCCTTGGCCTCCCAAAATGCTCGGATTACAGGCATGAGTCACTGCACCTGGCCA T G RPA2 Ensembl:ENSG00000117748 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6672392 Functional Loss SNV dbSNP153,EGP 33..33 33 - - - Human_RBP_ID_10910655,Human_RBP_ID_24678167 RMVar_hsa_circ_117034,RMVar_hsa_circ_91680,RMVar_hsa_circ_96066,RMVar_hsa_circ_130779,RMVar_hsa_circ_130781,RMVar_hsa_circ_130780,RMVar_hsa_circ_8731,RMVar_hsa_circ_366405,RMVar_hsa_circ_130784,RMVar_hsa_circ_298937,RMVar_hsa_circ_130786 9659 RMVar_ID_9659 Human_SNP_ID_7392040 A-to-I Human chr1 - 27899155 27899155 27899155 TTGGCCAGGCTGGTCTCGAACTCCTAACCTCAAGTGACTTGCTCGCCTTGGCCTCCCAAAATGCT TTGGCCAGGCTGGTCTCGAACTCCTAACCTCAGGTGACTTGCTCGCCTTGGCCTCCCAAAATGCT T C RPA2 Ensembl:ENSG00000117748 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs995060521 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10910655 RMVar_hsa_circ_117034,RMVar_hsa_circ_91680,RMVar_hsa_circ_96066,RMVar_hsa_circ_130779,RMVar_hsa_circ_130781,RMVar_hsa_circ_130780,RMVar_hsa_circ_8731,RMVar_hsa_circ_366405,RMVar_hsa_circ_130784,RMVar_hsa_circ_298937,RMVar_hsa_circ_130786 9660 RMVar_ID_9660 Human_SNP_ID_7392108 A-to-I Human chr1 - 27899377 27899377 27899377 CCTCAGCCTCCCGAGTAGCTGGGACTACAGGCACCCACCACCACACCTGGCTAATCTTTGCATTT CCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCCACCACCACACCTGGCTAATCTTTGCATTT T C RPA2 Ensembl:ENSG00000117748 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1158476385 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117034,RMVar_hsa_circ_91680,RMVar_hsa_circ_96066,RMVar_hsa_circ_130779,RMVar_hsa_circ_130781,RMVar_hsa_circ_130780,RMVar_hsa_circ_8731,RMVar_hsa_circ_366405,RMVar_hsa_circ_130784,RMVar_hsa_circ_298937,RMVar_hsa_circ_130786 9661 RMVar_ID_9661 Human_SNP_ID_7392547 A-to-I Human chr1 - 27900802 27900802 27900802 AATTTAGCTGGGCATGGTGGTACATGCCTGTAATCCTGGCTACTCGGGAGGGTGAGGCAGGAGAA AATTTAGCTGGGCATGGTGGTACATGCCTGTAGTCCTGGCTACTCGGGAGGGTGAGGCAGGAGAA T C RPA2 Ensembl:ENSG00000117748 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1285282325 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8307121 RMVar_hsa_circ_117034,RMVar_hsa_circ_91680,RMVar_hsa_circ_96066,RMVar_hsa_circ_130779,RMVar_hsa_circ_130781,RMVar_hsa_circ_130780,RMVar_hsa_circ_8731,RMVar_hsa_circ_366405,RMVar_hsa_circ_130784,RMVar_hsa_circ_298937,RMVar_hsa_circ_130786 9662 RMVar_ID_9662 Human_SNP_ID_7392950 A-to-I Human chr1 - 27902392 27902391 27902392 GTAGTCCCAGCTACTCGGGAGGCTGAGGCACAAGACTCGCTTGAACCCAGGAGGCAGAGGTTACA GTAGTCCCAGCTACTCGGGAGGCTGAGGCACA_GACTCGCTTGAACCCAGGAGGCAGAGGTTACA CT C RPA2 Ensembl:ENSG00000117748 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1220108235 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_117034,RMVar_hsa_circ_91680,RMVar_hsa_circ_96066,RMVar_hsa_circ_130779,RMVar_hsa_circ_130781,RMVar_hsa_circ_130780,RMVar_hsa_circ_8731,RMVar_hsa_circ_366405,RMVar_hsa_circ_130784,RMVar_hsa_circ_298937,RMVar_hsa_circ_130786 9663 RMVar_ID_9663 Human_SNP_ID_7393191 A-to-I Human chr1 - 27903487 27903487 27903487 CTCGAACTTTTGACCTCAGGTGATCCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCTTGAG CTCGAACTTTTGACCTCAGGTGATCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCTTGAG T C RPA2 Ensembl:ENSG00000117748 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs903700135 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117034,RMVar_hsa_circ_91680,RMVar_hsa_circ_96066,RMVar_hsa_circ_130779,RMVar_hsa_circ_130781,RMVar_hsa_circ_130780,RMVar_hsa_circ_8731,RMVar_hsa_circ_366405,RMVar_hsa_circ_130784,RMVar_hsa_circ_298937,RMVar_hsa_circ_130786 9664 RMVar_ID_9664 Human_SNP_ID_7393192 A-to-I Human chr1 - 27903487 27903487 27903487 CTCGAACTTTTGACCTCAGGTGATCCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCTTGAG CTCGAACTTTTGACCTCAGGTGATCCTGCCTCCGCCTCCCAAAGTGCTGGGATTACAGGCTTGAG T G RPA2 Ensembl:ENSG00000117748 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs903700135 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117034,RMVar_hsa_circ_91680,RMVar_hsa_circ_96066,RMVar_hsa_circ_130779,RMVar_hsa_circ_130781,RMVar_hsa_circ_130780,RMVar_hsa_circ_8731,RMVar_hsa_circ_366405,RMVar_hsa_circ_130784,RMVar_hsa_circ_298937,RMVar_hsa_circ_130786 9665 RMVar_ID_9665 Human_SNP_ID_7393513 A-to-I Human chr1 - 27904750 27904750 27904750 TGAGACAGAAAAATTGATTGAACCTAGGAGACAGAGGTTGCAGTGAGCCAAGATTGCGCCACTGC TGAGACAGAAAAATTGATTGAACCTAGGAGACGGAGGTTGCAGTGAGCCAAGATTGCGCCACTGC T C RPA2 Ensembl:ENSG00000117748 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1319753964 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10910772 RMVar_hsa_circ_117034,RMVar_hsa_circ_91680,RMVar_hsa_circ_96066,RMVar_hsa_circ_130779,RMVar_hsa_circ_130781,RMVar_hsa_circ_130780,RMVar_hsa_circ_8731,RMVar_hsa_circ_366405,RMVar_hsa_circ_130784,RMVar_hsa_circ_298937,RMVar_hsa_circ_130786 9666 RMVar_ID_9666 Human_SNP_ID_7393516 A-to-I Human chr1 - 27904757 27904757 27904757 CAGAAGCTGAGACAGAAAAATTGATTGAACCTAGGAGACAGAGGTTGCAGTGAGCCAAGATTGCG CAGAAGCTGAGACAGAAAAATTGATTGAACCTCGGAGACAGAGGTTGCAGTGAGCCAAGATTGCG T G RPA2 Ensembl:ENSG00000117748 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985392046 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10910772,Human_RBP_ID_24678249 RMVar_hsa_circ_117034,RMVar_hsa_circ_91680,RMVar_hsa_circ_96066,RMVar_hsa_circ_130779,RMVar_hsa_circ_130781,RMVar_hsa_circ_130780,RMVar_hsa_circ_8731,RMVar_hsa_circ_366405,RMVar_hsa_circ_130784,RMVar_hsa_circ_298937,RMVar_hsa_circ_130786 9667 RMVar_ID_9667 Human_SNP_ID_7393545 A-to-I Human chr1 - 27904883 27904883 27904883 CTTTGGGAGGCCAATGCTGGCGGGTCACCTGAAGTCAGAAGTTTGAAACCAGCCTGGCCAACGTG CTTTGGGAGGCCAATGCTGGCGGGTCACCTGATGTCAGAAGTTTGAAACCAGCCTGGCCAACGTG T A RPA2 Ensembl:ENSG00000117748 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1258222233 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10910776 RMVar_hsa_circ_117034,RMVar_hsa_circ_91680,RMVar_hsa_circ_96066,RMVar_hsa_circ_130779,RMVar_hsa_circ_130781,RMVar_hsa_circ_130780,RMVar_hsa_circ_8731,RMVar_hsa_circ_366405,RMVar_hsa_circ_130784,RMVar_hsa_circ_298937,RMVar_hsa_circ_130786 9668 RMVar_ID_9668 Human_SNP_ID_7393666 A-to-I Human chr1 - 27905434 27905434 27905434 CAAAAATTAGCCGGGCGTGGTTCTGCGCACCTATAATCCCAGCTACTCAGGAGGCTGAGGCAGGA CAAAAATTAGCCGGGCGTGGTTCTGCGCACCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGA T C RPA2 Ensembl:ENSG00000117748 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1201939675 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117034,RMVar_hsa_circ_91680,RMVar_hsa_circ_96066,RMVar_hsa_circ_130779,RMVar_hsa_circ_130781,RMVar_hsa_circ_130780,RMVar_hsa_circ_8731,RMVar_hsa_circ_366405,RMVar_hsa_circ_130784,RMVar_hsa_circ_298937,RMVar_hsa_circ_130786 9669 RMVar_ID_9669 Human_SNP_ID_7393698 A-to-I Human chr1 - 27905550 27905550 27905550 GAAGTGGCTCACGCCTGTAATCGCAACACTTTAGGAAGCCAAGGCAGGCAGATCACCTGAGGTCA GAAGTGGCTCACGCCTGTAATCGCAACACTTTTGGAAGCCAAGGCAGGCAGATCACCTGAGGTCA T A RPA2 Ensembl:ENSG00000117748 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs944943346 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557706 RMVar_hsa_circ_117034,RMVar_hsa_circ_91680,RMVar_hsa_circ_96066,RMVar_hsa_circ_130779,RMVar_hsa_circ_130781,RMVar_hsa_circ_130780,RMVar_hsa_circ_8731,RMVar_hsa_circ_366405,RMVar_hsa_circ_130784,RMVar_hsa_circ_298937,RMVar_hsa_circ_130786 9670 RMVar_ID_9670 Human_SNP_ID_7393897 A-to-I Human chr1 - 27906258 27906258 27906258 GGTTCAAGCAGTTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCACCCGCCACCACAC GGTTCAAGCAGTTCTCCTGCCTCAGCCTCCCAGGTAGCTGGGATTACAGGCACCCGCCACCACAC T C RPA2 Ensembl:ENSG00000117748 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs565547090 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117034,RMVar_hsa_circ_91680,RMVar_hsa_circ_96066,RMVar_hsa_circ_130779,RMVar_hsa_circ_130781,RMVar_hsa_circ_130780,RMVar_hsa_circ_8731,RMVar_hsa_circ_366405,RMVar_hsa_circ_130784,RMVar_hsa_circ_298937,RMVar_hsa_circ_130786 9671 RMVar_ID_9671 Human_SNP_ID_7394459 A-to-I Human chr1 - 27908349 27908349 27908349 AAGGTCGGAGGATCACTTGAGACCAAGAGTTTAAGACCAGCCTGGGCAACATAGCAAAACCCCAT AAGGTCGGAGGATCACTTGAGACCAAGAGTTTGAGACCAGCCTGGGCAACATAGCAAAACCCCAT T C RPA2 Ensembl:ENSG00000117748 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs999917237 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91680,RMVar_hsa_circ_96066,RMVar_hsa_circ_130781,RMVar_hsa_circ_130780,RMVar_hsa_circ_8731,RMVar_hsa_circ_358448 9672 RMVar_ID_9672 Human_SNP_ID_7394460 A-to-I Human chr1 - 27908349 27908349 27908349 AAGGTCGGAGGATCACTTGAGACCAAGAGTTTAAGACCAGCCTGGGCAACATAGCAAAACCCCAT AAGGTCGGAGGATCACTTGAGACCAAGAGTTTCAGACCAGCCTGGGCAACATAGCAAAACCCCAT T G RPA2 Ensembl:ENSG00000117748 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs999917237 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91680,RMVar_hsa_circ_96066,RMVar_hsa_circ_130781,RMVar_hsa_circ_130780,RMVar_hsa_circ_8731,RMVar_hsa_circ_358448 9673 RMVar_ID_9673 Human_SNP_ID_7394521 A-to-I Human chr1 - 27908588 27908588 27908588 GGGGGGCTGAGACAGGAGAATTGCTTGAACCCAGGAGATTGAGGTTGTAGTGAGCTGAGATCGCG GGGGGGCTGAGACAGGAGAATTGCTTGAACCCGGGAGATTGAGGTTGTAGTGAGCTGAGATCGCG T C RPA2 Ensembl:ENSG00000117748 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs560035274 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10910867 RMVar_hsa_circ_91680,RMVar_hsa_circ_96066,RMVar_hsa_circ_130781,RMVar_hsa_circ_130780,RMVar_hsa_circ_8731,RMVar_hsa_circ_358448 9674 RMVar_ID_9674 Human_SNP_ID_7394546 A-to-I Human chr1 - 27908637 27908637 27908637 GAAAAATTAGCTGGGCATGGTGGCGTGCACCTATAATCCCAGCTACTCGGGGGGGCTGAGACAGG GAAAAATTAGCTGGGCATGGTGGCGTGCACCTGTAATCCCAGCTACTCGGGGGGGCTGAGACAGG T C RPA2 Ensembl:ENSG00000117748 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs982842538 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24678295 RMVar_hsa_circ_91680,RMVar_hsa_circ_96066,RMVar_hsa_circ_130781,RMVar_hsa_circ_130780,RMVar_hsa_circ_8731,RMVar_hsa_circ_358448 9675 RMVar_ID_9675 Human_SNP_ID_7394785 A-to-I Human chr1 - 27909707 27909707 27909707 AGCGACCGCTCTTTTTTTTTTTTCTCTTTTTGAGGAGAGTCTCTGTTGCCCAGGCTGGAGTGCAA AGCGACCGCTCTTTTTTTTTTTTCTCTTTTTGTGGAGAGTCTCTGTTGCCCAGGCTGGAGTGCAA T A RPA2 Ensembl:ENSG00000117748 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1452097556 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11206796 RMVar_hsa_circ_91680,RMVar_hsa_circ_96066,RMVar_hsa_circ_130781,RMVar_hsa_circ_130780,RMVar_hsa_circ_8731,RMVar_hsa_circ_358448 9676 RMVar_ID_9676 Human_SNP_ID_7395537 A-to-I Human chr1 - 27913021 27913021 27913021 TTGAACTCTGGAGACAGAGATTGCAGTGAGCCAAGATGATGCCACTGCACTCCAGCCTGGGTGAT TTGAACTCTGGAGACAGAGATTGCAGTGAGCCCAGATGATGCCACTGCACTCCAGCCTGGGTGAT T G RPA2 Ensembl:ENSG00000117748 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1205827159 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91680,RMVar_hsa_circ_96066,RMVar_hsa_circ_130781,RMVar_hsa_circ_130780,RMVar_hsa_circ_8731,RMVar_hsa_circ_358448 9677 RMVar_ID_9677 Human_SNP_ID_7395540 A-to-I Human chr1 - 27913029 27913029 27913029 GGAATCGCTTGAACTCTGGAGACAGAGATTGCAGTGAGCCAAGATGATGCCACTGCACTCCAGCC GGAATCGCTTGAACTCTGGAGACAGAGATTGCTGTGAGCCAAGATGATGCCACTGCACTCCAGCC T A RPA2 Ensembl:ENSG00000117748 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1464494016 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91680,RMVar_hsa_circ_96066,RMVar_hsa_circ_130781,RMVar_hsa_circ_130780,RMVar_hsa_circ_8731,RMVar_hsa_circ_358448 9678 RMVar_ID_9678 Human_SNP_ID_7395541 A-to-I Human chr1 - 27913029 27913029 27913029 GGAATCGCTTGAACTCTGGAGACAGAGATTGCAGTGAGCCAAGATGATGCCACTGCACTCCAGCC GGAATCGCTTGAACTCTGGAGACAGAGATTGCGGTGAGCCAAGATGATGCCACTGCACTCCAGCC T C RPA2 Ensembl:ENSG00000117748 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1464494016 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91680,RMVar_hsa_circ_96066,RMVar_hsa_circ_130781,RMVar_hsa_circ_130780,RMVar_hsa_circ_8731,RMVar_hsa_circ_358448 9679 RMVar_ID_9679 Human_SNP_ID_7395543 A-to-I Human chr1 - 27913038 27913038 27913038 TGAAGCAGGGGAATCGCTTGAACTCTGGAGACAGAGATTGCAGTGAGCCAAGATGATGCCACTGC TGAAGCAGGGGAATCGCTTGAACTCTGGAGACCGAGATTGCAGTGAGCCAAGATGATGCCACTGC T G RPA2 Ensembl:ENSG00000117748 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1476039409 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91680,RMVar_hsa_circ_96066,RMVar_hsa_circ_130781,RMVar_hsa_circ_130780,RMVar_hsa_circ_8731,RMVar_hsa_circ_358448 9680 RMVar_ID_9680 Human_SNP_ID_7395714 A-to-I Human chr1 - 27913549 27913549 27913549 GAACCTCACTCTGTTGCCCAGGCTGGAGTGCAATGGCGCGATCTCGGCTCCCCGCAACCTCCGCC GAACCTCACTCTGTTGCCCAGGCTGGAGTGCAGTGGCGCGATCTCGGCTCCCCGCAACCTCCGCC T C RPA2 Ensembl:ENSG00000117748 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1264774396 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91680,RMVar_hsa_circ_96066,RMVar_hsa_circ_130781,RMVar_hsa_circ_130780,RMVar_hsa_circ_8731,RMVar_hsa_circ_358448 9681 RMVar_ID_9681 Human_SNP_ID_7410860 A-to-I Human chr1 - 27972962 27972961 27972963 CCTCAAGCGATCCTCCCACCTCGGCCTCTCAAAGTGTTGGGATTGTAGGCATGAGCCACTGCACC CCTCAAGCGATCCTCCCACCTCGGCCTCTCA__GTGTTGGGATTGTAGGCATGAGCCACTGCACC CTT C EYA3 Ensembl:ENSG00000158161 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1557513048 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_10911304 RMVar_hsa_circ_93827,RMVar_hsa_circ_130793 9682 RMVar_ID_9682 Human_SNP_ID_7411302 A-to-I Human chr1 - 27974896 27974896 27974896 CCAGCTACTCAGGATGCTGGAGTAAGAGGATTACCTGAGACCAGGGGTTCAAGGCCACAGTAAGC CCAGCTACTCAGGATGCTGGAGTAAGAGGATTGCCTGAGACCAGGGGTTCAAGGCCACAGTAAGC T C EYA3 Ensembl:ENSG00000158161 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1268954420 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93827,RMVar_hsa_circ_130793 9683 RMVar_ID_9683 Human_SNP_ID_7411728 A-to-I Human chr1 - 27976990 27976990 27976990 ATTGAGGCTGGGCACGGTGGCTCATGCCTATAATCCTAGCACTTGGGGAGGCTGAGGCAGGCAAA ATTGAGGCTGGGCACGGTGGCTCATGCCTATAGTCCTAGCACTTGGGGAGGCTGAGGCAGGCAAA T C EYA3 Ensembl:ENSG00000158161 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs544222513 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93827,RMVar_hsa_circ_130793 9684 RMVar_ID_9684 Human_SNP_ID_7411729 A-to-I Human chr1 - 27976993 27976993 27976993 TCCATTGAGGCTGGGCACGGTGGCTCATGCCTATAATCCTAGCACTTGGGGAGGCTGAGGCAGGC TCCATTGAGGCTGGGCACGGTGGCTCATGCCTGTAATCCTAGCACTTGGGGAGGCTGAGGCAGGC T C EYA3 Ensembl:ENSG00000158161 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1046006115 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19333605,Human_RBP_ID_24678376 RMVar_hsa_circ_93827,RMVar_hsa_circ_130793 9685 RMVar_ID_9685 Human_SNP_ID_7412709 A-to-I Human chr1 - 27981716 27981716 27981716 CAGGCTAGAGTTCAGTGATCACGACTCACTACAGCCTCGACCTCCCTGGCTCAAGCAACCCTCCC CAGGCTAGAGTTCAGTGATCACGACTCACTACGGCCTCGACCTCCCTGGCTCAAGCAACCCTCCC T C EYA3 Ensembl:ENSG00000158161 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs891835009 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4918,RMVar_hsa_circ_93827,RMVar_hsa_circ_341047,RMVar_hsa_circ_130793,RMVar_hsa_circ_363346,RMVar_hsa_circ_73064 9686 RMVar_ID_9686 Human_SNP_ID_7417312 A-to-I Human chr1 - 28002576 28002576 28002576 GAAATCTGAGGCTCAAGTGATTCTCCTGCCTCAGTCTCCCAAAGTGCTGTGATTATAGGCATGAG GAAATCTGAGGCTCAAGTGATTCTCCTGCCTCGGTCTCCCAAAGTGCTGTGATTATAGGCATGAG T C EYA3 Ensembl:ENSG00000158161 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1015464595 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4918,RMVar_hsa_circ_93827,RMVar_hsa_circ_130793,RMVar_hsa_circ_363346,RMVar_hsa_circ_73064,RMVar_hsa_circ_34067,RMVar_hsa_circ_19614,RMVar_hsa_circ_31434,RMVar_hsa_circ_276729,RMVar_hsa_circ_287105,RMVar_hsa_circ_41628,RMVar_hsa_circ_130795,RMVar_hsa_circ_130796,RMVar_hsa_circ_59009,RMVar_hsa_circ_370158,RMVar_hsa_circ_310621,RMVar_hsa_circ_356295,RMVar_hsa_circ_130797,RMVar_hsa_circ_299649,RMVar_hsa_circ_325850,RMVar_hsa_circ_130798,RMVar_hsa_circ_59745,RMVar_hsa_circ_319515 9687 RMVar_ID_9687 Human_SNP_ID_7421126 A-to-I Human chr1 - 28019114 28019114 28019114 TCGCCCAGGCTGGAGTGCAGTGGCGCGATCTCAGCTCACTGCAACCTCTGCCTCCCGAGTTTAAG TCGCCCAGGCTGGAGTGCAGTGGCGCGATCTCGGCTCACTGCAACCTCTGCCTCCCGAGTTTAAG T C EYA3 Ensembl:ENSG00000158161 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1345062602 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93827,RMVar_hsa_circ_130793,RMVar_hsa_circ_73064,RMVar_hsa_circ_5645,RMVar_hsa_circ_34067,RMVar_hsa_circ_31434,RMVar_hsa_circ_356295,RMVar_hsa_circ_61628,RMVar_hsa_circ_327161,RMVar_hsa_circ_328320,RMVar_hsa_circ_130800,RMVar_hsa_circ_36103,RMVar_hsa_circ_378277,RMVar_hsa_circ_130804 9688 RMVar_ID_9688 Human_SNP_ID_7428733 A-to-I Human chr1 - 28052267 28052267 28052267 GGGCGCAGTGGCTCATGCCTGTAATCCCAGCAATTTGGGAGGCCGAGGTGGGCAGATCACCTGAG GGGCGCAGTGGCTCATGCCTGTAATCCCAGCAGTTTGGGAGGCCGAGGTGGGCAGATCACCTGAG T C EYA3 Ensembl:ENSG00000158161 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs958543662 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73064,RMVar_hsa_circ_61628,RMVar_hsa_circ_331021,RMVar_hsa_circ_130808,RMVar_hsa_circ_130813,RMVar_hsa_circ_274925,RMVar_hsa_circ_294475,RMVar_hsa_circ_130818,RMVar_hsa_circ_130814,RMVar_hsa_circ_287514,RMVar_hsa_circ_130819,RMVar_hsa_circ_289984 9689 RMVar_ID_9689 Human_SNP_ID_7428865 A-to-I Human chr1 - 28052878 28052878 28052878 GGAGTGCAGTGTCACTATCTCGGCTCACTGCAACCTCCACCTCCCGGGTTCAGGTAGTTCCCTGC GGAGTGCAGTGTCACTATCTCGGCTCACTGCATCCTCCACCTCCCGGGTTCAGGTAGTTCCCTGC T A EYA3 Ensembl:ENSG00000158161 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1291189814 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73064,RMVar_hsa_circ_61628,RMVar_hsa_circ_331021,RMVar_hsa_circ_130808,RMVar_hsa_circ_130813,RMVar_hsa_circ_274925,RMVar_hsa_circ_294475,RMVar_hsa_circ_130818,RMVar_hsa_circ_130814,RMVar_hsa_circ_287514,RMVar_hsa_circ_130819,RMVar_hsa_circ_289984 9690 RMVar_ID_9690 Human_SNP_ID_7428866 A-to-I Human chr1 - 28052884 28052884 28052884 CAGGCTGGAGTGCAGTGTCACTATCTCGGCTCACTGCAACCTCCACCTCCCGGGTTCAGGTAGTT CAGGCTGGAGTGCAGTGTCACTATCTCGGCTCGCTGCAACCTCCACCTCCCGGGTTCAGGTAGTT T C EYA3 Ensembl:ENSG00000158161 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1437779358 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73064,RMVar_hsa_circ_61628,RMVar_hsa_circ_331021,RMVar_hsa_circ_130808,RMVar_hsa_circ_130813,RMVar_hsa_circ_274925,RMVar_hsa_circ_294475,RMVar_hsa_circ_130818,RMVar_hsa_circ_130814,RMVar_hsa_circ_287514,RMVar_hsa_circ_130819,RMVar_hsa_circ_289984 9691 RMVar_ID_9691 Human_SNP_ID_7429497 A-to-I Human chr1 - 28055563 28055563 28055563 GGGAAGCTGAGGCAGGAGAATCGCTTGAACCCAGGAGGTGGAGGTTGCAGTGAGCCGAGATTGTG GGGAAGCTGAGGCAGGAGAATCGCTTGAACCCGGGAGGTGGAGGTTGCAGTGAGCCGAGATTGTG T C EYA3 Ensembl:ENSG00000158161 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1009486867 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73064,RMVar_hsa_circ_61628,RMVar_hsa_circ_331021,RMVar_hsa_circ_130808,RMVar_hsa_circ_130813,RMVar_hsa_circ_274925,RMVar_hsa_circ_294475,RMVar_hsa_circ_130818,RMVar_hsa_circ_130814,RMVar_hsa_circ_287514,RMVar_hsa_circ_130819,RMVar_hsa_circ_289984 9692 RMVar_ID_9692 Human_SNP_ID_7430615 A-to-I Human chr1 - 28060962 28060962 28060962 GTCACCAAGCTGGAGTGCAGTGGTGCGATCTCAGCTCACTGAAACCTCCGCCTCCCAGGTTCACG GTCACCAAGCTGGAGTGCAGTGGTGCGATCTCGGCTCACTGAAACCTCCGCCTCCCAGGTTCACG T C EYA3 Ensembl:ENSG00000158161 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs571242700 Functional Loss SNV dbSNP153 33..33 33 - - - 9693 RMVar_ID_9693 Human_SNP_ID_7436869 A-to-I Human chr1 - 28086305 28086305 28086305 GGAGGTTGAGGTTGGAGGATTGCTTGAGCCCAAGATTTTGAGGTTACAGTGAGCTGTGATCACAT GGAGGTTGAGGTTGGAGGATTGCTTGAGCCCAGGATTTTGAGGTTACAGTGAGCTGTGATCACAT T C EYA3 Ensembl:ENSG00000158161 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1040901201 Functional Loss SNV dbSNP153 33..33 33 - - - 9694 RMVar_ID_9694 Human_SNP_ID_7470923 A-to-I Human chr1 - 28226249 28226249 28226249 TGCCTGCCTCGGCCTCTCAAAGTGCCGTGATTACAGACGTGAGCCACCACACCCAGATCTTTAAA TGCCTGCCTCGGCCTCTCAAAGTGCCGTGATTGCAGACGTGAGCCACCACACCCAGATCTTTAAA T C DNAJC8 Ensembl:ENSG00000126698 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1478556295 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10913656 9695 RMVar_ID_9695 Human_SNP_ID_7475455 A-to-I Human chr1 - 28243143 28243143 28243143 GAACTCCTGAGCTCAAGGGATCCTCCCGCCTCAGTCTCCCGAAGTACTGGCATTACAGGCGTGAG GAACTCCTGAGCTCAAGGGATCCTCCCGCCTCGGTCTCCCGAAGTACTGGCATTACAGGCGTGAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs548554737 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_130823 9696 RMVar_ID_9696 Human_SNP_ID_7475624 A-to-I Human chr1 - 28243796 28243796 28243796 AAACTTCTGGGCTCAGGTGATACTCCTGCCTCAGCCTCTGGAGTAACTGGGACTACATCTGAATG AAACTTCTGGGCTCAGGTGATACTCCTGCCTCGGCCTCTGGAGTAACTGGGACTACATCTGAATG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs948165241 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_130823 9697 RMVar_ID_9697 Human_SNP_ID_7476373 A-to-I Human chr1 - 28246974 28246974 28246974 CGGAGGTTGCAGTGAGCCGAGAACGCGCCACTACACTCCAGCCTGGACGACGAGAGTGATACTCC CGGAGGTTGCAGTGAGCCGAGAACGCGCCACTGCACTCCAGCCTGGACGACGAGAGTGATACTCC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1454366381 Functional Loss SNV dbSNP153 33..33 33 - - - 9698 RMVar_ID_9698 Human_SNP_ID_7486588 A-to-I Human chr1 + 28284809 28284809 28284809 TCCTGTAACCTTAGGTATTAATTCCATCCCACAGATAAGGAAATTGAGGAGGGAGTATTGAAGCA TCCTGTAACCTTAGGTATTAATTCCATCCCACGGATAAGGAAATTGAGGAGGGAGTATTGAAGCA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1008598574 Functional Loss SNV dbSNP153 33..33 33 - - - 9699 RMVar_ID_9699 Human_SNP_ID_7498148 A-to-I Human chr1 + 28330216 28330216 28330216 AGAATCGCTTGAACCTGGGAGGCAGAGGCTGCAGTGAACAGAGATTGCGCCATTGCACTCCAGCC AGAATCGCTTGAACCTGGGAGGCAGAGGCTGCGGTGAACAGAGATTGCGCCATTGCACTCCAGCC A G MED18 Ensembl:ENSG00000130772 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1406016182 Functional Loss SNV dbSNP153 33..33 33 - - - 9700 RMVar_ID_9700 Human_SNP_ID_7499364 A-to-I Human chr1 + 28335207 28335207 28335207 GGGATTACAGGCACATGCCACCATGCTCAGCTAATTTTTGTATTTTTAGTAGAAATGGGGATTCA GGGATTACAGGCACATGCCACCATGCTCAGCTCATTTTTGTATTTTTAGTAGAAATGGGGATTCA A C MED18 Ensembl:ENSG00000130772 Protein coding 3'UTR GSE47997;GSE99789 K562 cells&HepG2 cells;esophageal squamous carcinoma cells,EC109 - 23474544,29796672 RNA-Seq:(High) rs1039710837 Functional Loss SNV dbSNP153 33..33 33 - - - 9701 RMVar_ID_9701 Human_SNP_ID_7499365 A-to-I Human chr1 + 28335207 28335207 28335207 GGGATTACAGGCACATGCCACCATGCTCAGCTAATTTTTGTATTTTTAGTAGAAATGGGGATTCA GGGATTACAGGCACATGCCACCATGCTCAGCTGATTTTTGTATTTTTAGTAGAAATGGGGATTCA A G MED18 Ensembl:ENSG00000130772 Protein coding 3'UTR GSE47997;GSE99789 K562 cells&HepG2 cells;esophageal squamous carcinoma cells,EC109 - 23474544,29796672 RNA-Seq:(High) rs1039710837 Functional Loss SNV dbSNP153 33..33 33 - - - 9702 RMVar_ID_9702 Human_SNP_ID_7499368 A-to-I Human chr1 + 28335216 28335216 28335216 GGCACATGCCACCATGCTCAGCTAATTTTTGTATTTTTAGTAGAAATGGGGATTCACCATGTTGG GGCACATGCCACCATGCTCAGCTAATTTTTGTGTTTTTAGTAGAAATGGGGATTCACCATGTTGG A G MED18 Ensembl:ENSG00000130772 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1268011865 Functional Loss SNV dbSNP153 33..33 33 - - - 9703 RMVar_ID_9703 Human_SNP_ID_7499391 A-to-I Human chr1 + 28335301 28335301 28335301 TGACCTCGTGATCCACCCACCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCACGC TGACCTCGTGATCCACCCACCTTGGCCTCCCAGAGTGCTGGGATTACAGGCATGAGCCACCACGC A G MED18 Ensembl:ENSG00000130772 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1035288579 Functional Loss SNV dbSNP153 33..33 33 - - - 9704 RMVar_ID_9704 Human_SNP_ID_7499486 A-to-I Human chr1 + 28335701 28335701 28335701 AAATTTAGCCGGGCATGGTAGCAGGCGCTTGTAATCCCAGCTACTTGGGAGGCTGAGGCTGGAGA AAATTTAGCCGGGCATGGTAGCAGGCGCTTGTCATCCCAGCTACTTGGGAGGCTGAGGCTGGAGA A C MED18 Ensembl:ENSG00000130772 Protein coding 3'UTR GSE38233;GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,32596459 RNA-Seq:(High) rs752418310 Functional Loss SNV dbSNP153 33..33 33 - - - 9705 RMVar_ID_9705 Human_SNP_ID_7499488 A-to-I Human chr1 + 28335711 28335711 28335711 GGGCATGGTAGCAGGCGCTTGTAATCCCAGCTACTTGGGAGGCTGAGGCTGGAGAATCGCTTGAA GGGCATGGTAGCAGGCGCTTGTAATCCCAGCTGCTTGGGAGGCTGAGGCTGGAGAATCGCTTGAA A G MED18 Ensembl:ENSG00000130772 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1345860466 Functional Loss SNV dbSNP153 33..33 33 - - - 9706 RMVar_ID_9706 Human_SNP_ID_7499499 A-to-I Human chr1 + 28335742 28335742 28335742 TACTTGGGAGGCTGAGGCTGGAGAATCGCTTGAACCCAGGAGGTGAAGGTTGCAGTGACCAGAGA TACTTGGGAGGCTGAGGCTGGAGAATCGCTTGGACCCAGGAGGTGAAGGTTGCAGTGACCAGAGA A G MED18 Ensembl:ENSG00000130772 Protein coding 3'UTR GSE38233;GSE100210;GSE100210;GSE99789;GSE107867;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;HepG2 cell line;esophageal squamous carcinoma cells,EC109;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,29129909,29796672,30559470,32596459 RNA-Seq:(High) rs1131732 Functional Loss SNV dbSNP153 33..33 33 - - - 9707 RMVar_ID_9707 Human_SNP_ID_7499507 A-to-I Human chr1 + 28335770 28335770 28335770 CTTGAACCCAGGAGGTGAAGGTTGCAGTGACCAGAGATGACGCCATTGCACTCCAGCCTGGGTGA CTTGAACCCAGGAGGTGAAGGTTGCAGTGACCGGAGATGACGCCATTGCACTCCAGCCTGGGTGA A G MED18 Ensembl:ENSG00000130772 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1131733 Functional Loss SNV dbSNP153 33..33 33 - - - 9708 RMVar_ID_9708 Human_SNP_ID_7518818 A-to-I Human chr1 + 28408869 28408869 28408869 GACTGATTTTTTTTTTTTTTTTTGGTAGAGATAGGGCTTTGCCTTGTTGAGCAGGCGGCTCTGGA GACTGATTTTTTTTTTTTTTTTTGGTAGAGATGGGGCTTTGCCTTGTTGAGCAGGCGGCTCTGGA A G PHACTR4 Ensembl:ENSG00000204138 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404220128 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_272713,Human_RBP_ID_10915207,Human_RBP_ID_24763412 RMVar_hsa_circ_11475,RMVar_hsa_circ_286134,RMVar_hsa_circ_130837,RMVar_hsa_circ_130838 9709 RMVar_ID_9709 Human_SNP_ID_7522051 A-to-I Human chr1 + 28422819 28422819 28422819 ACTAGAGACTTCTTTTTTTGAGACAGAGTCTCACTCTGTCGCCAGGCTGGAGTGCAGTGGTGCCA ACTAGAGACTTCTTTTTTTGAGACAGAGTCTCTCTCTGTCGCCAGGCTGGAGTGCAGTGGTGCCA A T PHACTR4 Ensembl:ENSG00000204138 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1268534015 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11475,RMVar_hsa_circ_286134,RMVar_hsa_circ_130838 9710 RMVar_ID_9710 Human_SNP_ID_7527537 A-to-I Human chr1 + 28445849 28445849 28445849 CCAGGAGGTTGAGGCTGCAGTGAGCCATGATCATGTCACTGCACTGCAGCCTGGCTAACAGAGCG CCAGGAGGTTGAGGCTGCAGTGAGCCATGATCTTGTCACTGCACTGCAGCCTGGCTAACAGAGCG A T PHACTR4 Ensembl:ENSG00000204138 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444303423 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11475,RMVar_hsa_circ_286134,RMVar_hsa_circ_130838 9711 RMVar_ID_9711 Human_SNP_ID_7527538 A-to-I Human chr1 + 28445859 28445859 28445859 GAGGCTGCAGTGAGCCATGATCATGTCACTGCACTGCAGCCTGGCTAACAGAGCGAGACTGTGTT GAGGCTGCAGTGAGCCATGATCATGTCACTGCGCTGCAGCCTGGCTAACAGAGCGAGACTGTGTT A G PHACTR4 Ensembl:ENSG00000204138 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1260684357 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11475,RMVar_hsa_circ_286134,RMVar_hsa_circ_130838 9712 RMVar_ID_9712 Human_SNP_ID_7527539 A-to-I Human chr1 + 28445859 28445859 28445859 GAGGCTGCAGTGAGCCATGATCATGTCACTGCACTGCAGCCTGGCTAACAGAGCGAGACTGTGTT GAGGCTGCAGTGAGCCATGATCATGTCACTGCTCTGCAGCCTGGCTAACAGAGCGAGACTGTGTT A T PHACTR4 Ensembl:ENSG00000204138 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1260684357 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11475,RMVar_hsa_circ_286134,RMVar_hsa_circ_130838 9713 RMVar_ID_9713 Human_SNP_ID_7534160 A-to-I Human chr1 + 28472628 28472627 28472629 GTTATACAAAATAACTTTTTTTTTTTTGAGTCAGAGTCTTGTGCTGTCCAGCCTGGAGTGCAGTG GTTATACAAAATAACTTTTTTTTTTTTGAGTC__AGTCTTGTGCTGTCCAGCCTGGAGTGCAGTG CAG C PHACTR4 Ensembl:ENSG00000204138 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432868870 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_11475,RMVar_hsa_circ_71399,RMVar_hsa_circ_58797 9714 RMVar_ID_9714 Human_SNP_ID_7534799 A-to-I Human chr1 + 28474677 28474677 28474677 CGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGAGACTACAGGCATGTGCCACCACATTCGGCTGA CGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGTGACTACAGGCATGTGCCACCACATTCGGCTGA A T PHACTR4 Ensembl:ENSG00000204138 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1412457749 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11475,RMVar_hsa_circ_58797,RMVar_hsa_circ_130843,RMVar_hsa_circ_112572,RMVar_hsa_circ_272417,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 9715 RMVar_ID_9715 Human_SNP_ID_7534800 A-to-I Human chr1 + 28474688 28474688 28474688 CCTCAGCCTCCCGAGTAGCTGAGACTACAGGCATGTGCCACCACATTCGGCTGATTTTTGTATTT CCTCAGCCTCCCGAGTAGCTGAGACTACAGGCGTGTGCCACCACATTCGGCTGATTTTTGTATTT A G PHACTR4 Ensembl:ENSG00000204138 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs892614515 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11475,RMVar_hsa_circ_58797,RMVar_hsa_circ_130843,RMVar_hsa_circ_112572,RMVar_hsa_circ_272417,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 9716 RMVar_ID_9716 Human_SNP_ID_7537210 A-to-I Human chr1 + 28484246 28484246 28484246 AGGACACTGAGGCAAGAGAATCACTTGAACCCAGGAGGCAGAGGTTTCAGTGAGCTGAGATCACA AGGACACTGAGGCAAGAGAATCACTTGAACCCCGGAGGCAGAGGTTTCAGTGAGCTGAGATCACA A C PHACTR4 Ensembl:ENSG00000204138 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs566910422 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112572,RMVar_hsa_circ_369863,RMVar_hsa_circ_116363,RMVar_hsa_circ_130845,RMVar_hsa_circ_130846,RMVar_hsa_circ_130847,RMVar_hsa_circ_67275,RMVar_hsa_circ_300506,RMVar_hsa_circ_352202,RMVar_hsa_circ_43590,RMVar_hsa_circ_130850,RMVar_hsa_circ_130851,RMVar_hsa_circ_130849,RMVar_hsa_circ_130853,RMVar_hsa_circ_130854,RMVar_hsa_circ_300213,RMVar_hsa_circ_322526,RMVar_hsa_circ_339659 9717 RMVar_ID_9717 Human_SNP_ID_7540803 A-to-I Human chr1 + 28497809 28497809 28497809 GAGTTCAGGAGTTCAAGACCAGCCTGGCCAACATGGCAAAACCCTGTCTCTACTAAAAAGTAAAA GAGTTCAGGAGTTCAAGACCAGCCTGGCCAACGTGGCAAAACCCTGTCTCTACTAAAAAGTAAAA A G PHACTR4 Ensembl:ENSG00000204138 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1180228141 Functional Loss SNV dbSNP153 33..33 33 - - - 9718 RMVar_ID_9718 Human_SNP_ID_7541029 A-to-I Human chr1 + 28498884 28498884 28498884 GCGGTCAGGAGTTTGAGACCAGCCTGACCAACATGATGAAACCCTGTCTCTACTAAAAATACAAA GCGGTCAGGAGTTTGAGACCAGCCTGACCAACGTGATGAAACCCTGTCTCTACTAAAAATACAAA A G PHACTR4 Ensembl:ENSG00000204138 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1425703111 Functional Loss SNV dbSNP153 33..33 33 - - - 9719 RMVar_ID_9719 Human_SNP_ID_7541054 A-to-I Human chr1 + 28498974 28498974 28498974 TCTGTAATCCCAACTACTCAGGACGCTGAGGCAGGAGAGTCGCTTGAACCCAGGAGGCGGAGATT TCTGTAATCCCAACTACTCAGGACGCTGAGGCGGGAGAGTCGCTTGAACCCAGGAGGCGGAGATT A G PHACTR4 Ensembl:ENSG00000204138 Protein coding 3'UTR GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,29796672,31158229,31158229,31158229 RNA-Seq:(High) rs1354738099 Functional Loss SNV dbSNP153 33..33 33 - - - 9720 RMVar_ID_9720 Human_SNP_ID_7541145 A-to-I Human chr1 + 28499269 28499269 28499269 GCGATTCTCCTACCTCAGCCTCCCAAGTAGCTAGGATTACAGGCATGAGCCACCACGCCTGGCTA GCGATTCTCCTACCTCAGCCTCCCAAGTAGCTGGGATTACAGGCATGAGCCACCACGCCTGGCTA A G PHACTR4 Ensembl:ENSG00000204138 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1292899769 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_103470 9721 RMVar_ID_9721 Human_SNP_ID_7541218 A-to-I Human chr1 + 28499503 28499503 28499503 GTTTTGTTTTGTTTTGTTTTGTTTTTGGAGATAGGGTCTCACTCTGTTACCCATGCTGGAGTGCA GTTTTGTTTTGTTTTGTTTTGTTTTTGGAGATGGGGTCTCACTCTGTTACCCATGCTGGAGTGCA A G PHACTR4 Ensembl:ENSG00000204138 Protein coding 3'UTR GSE38233;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29796672,31158229,31158229,32596459,32596459 RNA-Seq:(High) rs1260073684 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5805399,Human_RBP_ID_26385672 9722 RMVar_ID_9722 Human_SNP_ID_7541220 A-to-I Human chr1 + 28499519 28499504 28499520 TTTTGTTTTTGGAGATAGGGTCTCACTCTGTTACCCATGCTGGAGTGCAGTGGCACAATCTTGGC TTTTGTTTTTGGAGATAG________________CCATGCTGGAGTGCAGTGGCACAATCTTGGC GGGTCTCACTCTGTTAC G PHACTR4 Ensembl:ENSG00000204138 Protein coding 3'UTR GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29796672,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs1557859283 Functional Loss DEL dbSNP153 19..34 33 - - - Human_RBP_ID_26385672 Human_miRNA_ID_479129 9723 RMVar_ID_9723 Human_SNP_ID_7541221 A-to-I Human chr1 + 28499511 28499511 28499511 TTGTTTTGTTTTGTTTTTGGAGATAGGGTCTCACTCTGTTACCCATGCTGGAGTGCAGTGGCACA TTGTTTTGTTTTGTTTTTGGAGATAGGGTCTCTCTCTGTTACCCATGCTGGAGTGCAGTGGCACA A T PHACTR4 Ensembl:ENSG00000204138 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs145120337 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5805401,Human_RBP_ID_26385672 9724 RMVar_ID_9724 Human_SNP_ID_7541237 A-to-I Human chr1 + 28499602 28499602 28499602 CCCAGGCTCAAGCAATCCTCCCACTTCAGTCTAAGTAGCTGGGACTACAGGCACGTGCCACCAGG CCCAGGCTCAAGCAATCCTCCCACTTCAGTCTGAGTAGCTGGGACTACAGGCACGTGCCACCAGG A G PHACTR4 Ensembl:ENSG00000204138 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1129047 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26385672 Human_miRNA_ID_344434 9725 RMVar_ID_9725 Human_SNP_ID_7541251 A-to-I Human chr1 + 28499678 28499678 28499678 TTTGTGTTTTGTTAGAGATGAGGTTTTGCCATATTGCCCAGGCTCGTCTTGAACACCGGGGCTCA TTTGTGTTTTGTTAGAGATGAGGTTTTGCCATGTTGCCCAGGCTCGTCTTGAACACCGGGGCTCA A G PHACTR4 Ensembl:ENSG00000204138 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1129048 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4042953,Human_RBP_ID_10916309,Human_RBP_ID_17557062,Human_RBP_ID_26378638 9726 RMVar_ID_9726 Human_SNP_ID_7541272 A-to-I Human chr1 + 28499749 28499749 28499749 CTGCCCATCTTCGCCTCCCAAAGTTCTGAGATAGCAGGTGTGAGTCATCATGCCCAGCCTCCTTG CTGCCCATCTTCGCCTCCCAAAGTTCTGAGATGGCAGGTGTGAGTCATCATGCCCAGCCTCCTTG A G PHACTR4 Ensembl:ENSG00000204138 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1129049 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_351094,Human_RBP_ID_17558327,Human_RBP_ID_26387788 Human_miRNA_ID_1092140 9727 RMVar_ID_9727 Human_SNP_ID_7542115 A-to-I Human chr1 - 28503607 28503607 28503607 ATGTTAGCTGAGTGTAGTGGCACATTCCTGTAATCCTAGCTACTTATGAGGTGTGAGGATCACCT ATGTTAGCTGAGTGTAGTGGCACATTCCTGTACTCCTAGCTACTTATGAGGTGTGAGGATCACCT T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1476406333 Functional Loss SNV dbSNP153 33..33 33 - - - 9728 RMVar_ID_9728 Human_SNP_ID_7542723 A-to-I Human chr1 - 28505661 28505660 28505661 CGCCTGTGATTACAGCAGCTCTGAAGGCCGTGAGGGGCGGATCGCTTGAGGCCAGGAGTTCGAGA CGCCTGTGATTACAGCAGCTCTGAAGGCCGTG_GGGGCGGATCGCTTGAGGCCAGGAGTTCGAGA CT C lnc-TAF12-6 RNACentral:URS0000D5DF79 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1208776415 Functional Loss DEL dbSNP153 33..33 33 - - - 9729 RMVar_ID_9729 Human_SNP_ID_7544396 A-to-I Human chr1 + 28509335 28509335 28509335 CATGATCTTGCTCACTGCAACTTCCGCCTCCCAGGTTCAGGCGATTCTCCTGCCTCAGCCTCCCA CATGATCTTGCTCACTGCAACTTCCGCCTCCCGGGTTCAGGCGATTCTCCTGCCTCAGCCTCCCA A G RCC1,SNHG3 Ensembl:ENSG00000180198,Ensembl:ENSG00000242125 Protein coding,lincRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1131661 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_351136,Human_RBP_ID_5091977,Human_RBP_ID_5161438,Human_RBP_ID_8242400,Human_RBP_ID_8307340,Human_RBP_ID_8747786 Human_miRNA_ID_2722961,Human_miRNA_ID_3192415 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 9730 RMVar_ID_9730 Human_SNP_ID_7544429 A-to-I Human chr1 + 28509422 28509422 28509422 TAGCACCACACCTGGCTAATTTTTGTATTTTTAGTAGAGATGAGGTTTCACCATATTGGCCAGGC TAGCACCACACCTGGCTAATTTTTGTATTTTTGGTAGAGATGAGGTTTCACCATATTGGCCAGGC A G RCC1,SNHG3 Ensembl:ENSG00000180198,Ensembl:ENSG00000242125 Protein coding,lincRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1131664 Functional Loss SNV dbSNP153 33..33 33 - - - 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 9731 RMVar_ID_9731 Human_SNP_ID_7544457 A-to-I Human chr1 + 28509486 28509486 28509486 CTGTTCTCAACTCCTGACCTCGTGATCCGCCCACCTCAGCCTCCTAAAGTGCTGGGATTACAGCT CTGTTCTCAACTCCTGACCTCGTGATCCGCCCGCCTCAGCCTCCTAAAGTGCTGGGATTACAGCT A G RCC1,SNHG3 Ensembl:ENSG00000180198,Ensembl:ENSG00000242125 Protein coding,lincRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs577173355 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_351141,Human_RBP_ID_1438458,Human_RBP_ID_3334832,Human_RBP_ID_10916582 Human_miRNA_ID_2712111,Human_miRNA_ID_2872275,Human_miRNA_ID_2980240,Human_miRNA_ID_3048099,Human_miRNA_ID_3191718,Human_miRNA_ID_3201494,Human_miRNA_ID_3207805,Human_miRNA_ID_3211909 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 9732 RMVar_ID_9732 Human_SNP_ID_7544470 A-to-I Human chr1 + 28509515 28509515 28509515 CCCACCTCAGCCTCCTAAAGTGCTGGGATTACAGCTGTGAGCCACCCTGCCCGGCCACTTTTGTA CCCACCTCAGCCTCCTAAAGTGCTGGGATTACGGCTGTGAGCCACCCTGCCCGGCCACTTTTGTA A G RCC1,SNHG3 Ensembl:ENSG00000180198,Ensembl:ENSG00000242125 Protein coding,lincRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1378297243 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_351142,Human_RBP_ID_1153888,Human_RBP_ID_1438458,Human_RBP_ID_1744590,Human_RBP_ID_2141701,Human_RBP_ID_3309048,Human_RBP_ID_5805566,Human_RBP_ID_8307342,Human_RBP_ID_10916585,Human_RBP_ID_22140777,Human_RBP_ID_22861449,Human_RBP_ID_24679895 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 9733 RMVar_ID_9733 Human_SNP_ID_7544788 A-to-I Human chr1 + 28510382 28510382 28510382 AAATGCAGCCAGGCTTGGTGGCTCACACCCGTAATCCCAGCACTTAGGCTAAGGCAGGCGGATCA AAATGCAGCCAGGCTTGGTGGCTCACACCCGTCATCCCAGCACTTAGGCTAAGGCAGGCGGATCA A C RCC1,SNHG3 Ensembl:ENSG00000180198,Ensembl:ENSG00000242125 Protein coding,lincRNA intron,exon GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs781370630 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3334839,Human_RBP_ID_8171858,Human_RBP_ID_8243708,Human_RBP_ID_10916641 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 9734 RMVar_ID_9734 Human_SNP_ID_7544789 A-to-I Human chr1 + 28510388 28510388 28510388 AGCCAGGCTTGGTGGCTCACACCCGTAATCCCAGCACTTAGGCTAAGGCAGGCGGATCACAACAT AGCCAGGCTTGGTGGCTCACACCCGTAATCCCGGCACTTAGGCTAAGGCAGGCGGATCACAACAT A G RCC1,SNHG3 Ensembl:ENSG00000180198,Ensembl:ENSG00000242125 Protein coding,lincRNA intron,exon GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs745848556 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8171858,Human_RBP_ID_8243708,Human_RBP_ID_10916641 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 9735 RMVar_ID_9735 Human_SNP_ID_7544794 A-to-I Human chr1 + 28510400 28510400 28510400 TGGCTCACACCCGTAATCCCAGCACTTAGGCTAAGGCAGGCGGATCACAACATCTAGAGATCCTG TGGCTCACACCCGTAATCCCAGCACTTAGGCTGAGGCAGGCGGATCACAACATCTAGAGATCCTG A G RCC1,SNHG3 Ensembl:ENSG00000180198,Ensembl:ENSG00000242125 Protein coding,lincRNA intron,exon GSE38233;GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,31158229,31158229,32596459 RNA-Seq:(High) rs1047129388 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8243708,Human_RBP_ID_10916641 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 9736 RMVar_ID_9736 Human_SNP_ID_7544815 A-to-I Human chr1 + 28510446 28510446 28510446 ACAACATCTAGAGATCCTGGCCAACGCGGTGAAACCCTGTCTGTACTAAAAATACAAAATAACTG ACAACATCTAGAGATCCTGGCCAACGCGGTGATACCCTGTCTGTACTAAAAATACAAAATAACTG A T RCC1,SNHG3 Ensembl:ENSG00000180198,Ensembl:ENSG00000242125 Protein coding,lincRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005695540 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5805601,Human_RBP_ID_10916641,Human_RBP_ID_17557063 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 9737 RMVar_ID_9737 Human_SNP_ID_7544822 A-to-I Human chr1 + 28510467 28510467 28510467 CAACGCGGTGAAACCCTGTCTGTACTAAAAATACAAAATAACTGGGCATGGTGGTGTGCACCTGT CAACGCGGTGAAACCCTGTCTGTACTAAAAATGCAAAATAACTGGGCATGGTGGTGTGCACCTGT A G RCC1,SNHG3 Ensembl:ENSG00000180198,Ensembl:ENSG00000242125 Protein coding,lincRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs3202298 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9512409,Human_RBP_ID_10916665,Human_RBP_ID_17557063 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 9738 RMVar_ID_9738 Human_SNP_ID_7545883 A-to-I Human chr1 + 28513463 28513463 28513463 GCAGTCCGCCTGCCCTGACCTCCCAAAGTGCTAGAATTACAGGCATGAGCCACCGTGCCTGGCCT GCAGTCCGCCTGCCCTGACCTCCCAAAGTGCTGGAATTACAGGCATGAGCCACCGTGCCTGGCCT A G RCC1 Ensembl:ENSG00000180198 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1456682604 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35000,RMVar_hsa_circ_71527 9739 RMVar_ID_9739 Human_SNP_ID_7546008 A-to-I Human chr1 + 28513977 28513977 28513977 GTAGTATAAGAATCTTCCCCAGCCTGGCCAATATGGTGAAACCCCGCCTCTACTAAAAATACAAA GTAGTATAAGAATCTTCCCCAGCCTGGCCAATGTGGTGAAACCCCGCCTCTACTAAAAATACAAA A G RCC1 Ensembl:ENSG00000180198 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1470443953 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35000,RMVar_hsa_circ_71527 9740 RMVar_ID_9740 Human_SNP_ID_7546047 A-to-I Human chr1 + 28514099 28514099 28514099 GCTGAGGCAGAAGATTGCTTGAACCTGGAAGCAGAGGTTGCAGTGAGCTGAGATCGTGCCAGCCT GCTGAGGCAGAAGATTGCTTGAACCTGGAAGCGGAGGTTGCAGTGAGCTGAGATCGTGCCAGCCT A G RCC1 Ensembl:ENSG00000180198 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1250339459 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10916859,Human_RBP_ID_17558329 RMVar_hsa_circ_35000,RMVar_hsa_circ_71527 9741 RMVar_ID_9741 Human_SNP_ID_7546061 A-to-I Human chr1 + 28514132 28514132 28514132 GAGGTTGCAGTGAGCTGAGATCGTGCCAGCCTAGGCAACAGAGCAAGACTCCGTCTCAAAAAAAA GAGGTTGCAGTGAGCTGAGATCGTGCCAGCCTGGGCAACAGAGCAAGACTCCGTCTCAAAAAAAA A G RCC1 Ensembl:ENSG00000180198 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1472091375 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10916859 RMVar_hsa_circ_35000,RMVar_hsa_circ_71527 9742 RMVar_ID_9742 Human_SNP_ID_7549635 A-to-I Human chr1 + 28527477 28527477 28527477 GTTGCCCACGCTGGTCTTGAACTCCTGGGCTCAAGCGATCCTCCTGCCTCGACTTCCCAAAGTGC GTTGCCCACGCTGGTCTTGAACTCCTGGGCTCCAGCGATCCTCCTGCCTCGACTTCCCAAAGTGC A C RCC1 Ensembl:ENSG00000180198 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1436876560 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35000,RMVar_hsa_circ_78460,RMVar_hsa_circ_49629,RMVar_hsa_circ_130867 9743 RMVar_ID_9743 Human_SNP_ID_7549761 A-to-I Human chr1 + 28527941 28527941 28527941 TGAGGCAGGAGAATCACTTGAACCTGGGAGGTAGAGGTTGTGGTGAGCCGAGATTGCGCCATGGC TGAGGCAGGAGAATCACTTGAACCTGGGAGGTGGAGGTTGTGGTGAGCCGAGATTGCGCCATGGC A G RCC1 Ensembl:ENSG00000180198 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1278827006 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22562689 RMVar_hsa_circ_35000,RMVar_hsa_circ_78460,RMVar_hsa_circ_49629,RMVar_hsa_circ_130867 9744 RMVar_ID_9744 Human_SNP_ID_7549967 A-to-I Human chr1 + 28528507 28528507 28528507 AAACTTAGCAGGGCATGGTGATGCACACCTGTAATCTCAGCTACTCGGAAGGCTGAGGCACAAGA AAACTTAGCAGGGCATGGTGATGCACACCTGTGATCTCAGCTACTCGGAAGGCTGAGGCACAAGA A G RCC1 Ensembl:ENSG00000180198 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1025179650 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10917399 RMVar_hsa_circ_35000,RMVar_hsa_circ_78460,RMVar_hsa_circ_49629,RMVar_hsa_circ_130867 9745 RMVar_ID_9745 Human_SNP_ID_7551003 A-to-I Human chr1 + 28531284 28531284 28531284 TTCTTTTCTTTTTCTTTTTTTTTTTTTTTTTGAGATCAAGTATCACTCTGTCGCCCAGACTGGAG TTCTTTTCTTTTTCTTTTTTTTTTTTTTTTTGTGATCAAGTATCACTCTGTCGCCCAGACTGGAG A T RCC1 Ensembl:ENSG00000180198 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1302152902 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5805806,Human_RBP_ID_10917485,Human_RBP_ID_22783952,Human_RBP_ID_23303960 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 9746 RMVar_ID_9746 Human_SNP_ID_7553388 A-to-I Human chr1 + 28539486 28539485 28539487 TGGCTAAATTTTTTTGTGTTTTTAGTAGAGACAGGGTCTTGCCCCGTTGGTCAGGCTGGTCCCGA TGGCTAAATTTTTTTGTGTTTTTAGTAGAGAC__GGTCTTGCCCCGTTGGTCAGGCTGGTCCCGA CAG C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1311155040 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_1347995,Human_RBP_ID_10917733 9747 RMVar_ID_9747 Human_SNP_ID_7554832 A-to-I Human chr1 + 28543570 28543570 28543570 TCAGGTGATCCTCCCACCTCAGCCTCCCAAGTAGCTGGGACCATAGGCATGTGTCACTACACTTG TCAGGTGATCCTCCCACCTCAGCCTCCCAAGTGGCTGGGACCATAGGCATGTGTCACTACACTTG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1287030778 Functional Loss SNV dbSNP153 33..33 33 - - - 9748 RMVar_ID_9748 Human_SNP_ID_7554840 A-to-I Human chr1 + 28543615 28543615 28543615 GGCATGTGTCACTACACTTGGCTAATTTTTGTATTTGTTTGTAGCTACAGGGTTTTGCCACGATG GGCATGTGTCACTACACTTGGCTAATTTTTGTGTTTGTTTGTAGCTACAGGGTTTTGCCACGATG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1227419428 Functional Loss SNV dbSNP153 33..33 33 - - - 9749 RMVar_ID_9749 Human_SNP_ID_7554844 A-to-I Human chr1 + 28543631 28543631 28543631 CTTGGCTAATTTTTGTATTTGTTTGTAGCTACAGGGTTTTGCCACGATGTACAGGCTGGTGTCGA CTTGGCTAATTTTTGTATTTGTTTGTAGCTACGGGGTTTTGCCACGATGTACAGGCTGGTGTCGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs561434753 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8307443 9750 RMVar_ID_9750 Human_SNP_ID_7558200 A-to-I Human chr1 + 28555576 28555576 28555576 TTGGAGTGCAGTGGCGCGATCTTGGCTCACTGAAAGCTCCGCCTCCTGGGTTCACGCCATTCTCC TTGGAGTGCAGTGGCGCGATCTTGGCTCACTGCAAGCTCCGCCTCCTGGGTTCACGCCATTCTCC A C TRNAU1AP Ensembl:ENSG00000180098 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1421069321 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_46181,RMVar_hsa_circ_338370,RMVar_hsa_circ_130871,RMVar_hsa_circ_130872 9751 RMVar_ID_9751 Human_SNP_ID_7559345 A-to-I Human chr1 + 28559481 28559481 28559481 AGAAACCCCATCTCTACTGAAAATACAAAATTAGCTGGGCATGGTGGCGCATGCCTGTAATTCCA AGAAACCCCATCTCTACTGAAAATACAAAATTTGCTGGGCATGGTGGCGCATGCCTGTAATTCCA A T TRNAU1AP Ensembl:ENSG00000180098 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1397228958 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_46181,RMVar_hsa_circ_338370,RMVar_hsa_circ_130871,RMVar_hsa_circ_130872 9752 RMVar_ID_9752 Human_SNP_ID_7559460 A-to-I Human chr1 + 28559953 28559944 28559953 CAGGAGTTCAAGATCAGCCTGGCCAACATGGCAAAATCCCATCTCTACTAAAAATACAAAAATTA CAGGAGTTCAAGATCAGCCTGGCC_________AAATCCCATCTCTACTAAAAATACAAAAATTA CAACATGGCA C TRNAU1AP Ensembl:ENSG00000180098 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1196824756 Functional Loss DEL dbSNP153 25..33 33 - - - RMVar_hsa_circ_46181,RMVar_hsa_circ_338370,RMVar_hsa_circ_130871,RMVar_hsa_circ_130872 9753 RMVar_ID_9753 Human_SNP_ID_7559465 A-to-I Human chr1 + 28559989 28559989 28559989 TCCCATCTCTACTAAAAATACAAAAATTAGCCAGGCATGGTGGTGGGTACCTGTAATTCCAAGTG TCCCATCTCTACTAAAAATACAAAAATTAGCCCGGCATGGTGGTGGGTACCTGTAATTCCAAGTG A C TRNAU1AP Ensembl:ENSG00000180098 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs764138868 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_46181,RMVar_hsa_circ_338370,RMVar_hsa_circ_130871,RMVar_hsa_circ_130872 9754 RMVar_ID_9754 Human_SNP_ID_7561786 A-to-I Human chr1 + 28568464 28568464 28568464 TGCTAGGCAAATTTTGTGTTTTTTGTAGAGATAGGGTCTTGCTTTGTTGCCCAGGCTGGTTTCGA TGCTAGGCAAATTTTGTGTTTTTTGTAGAGATGGGGTCTTGCTTTGTTGCCCAGGCTGGTTTCGA A G TRNAU1AP Ensembl:ENSG00000180098 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs568183879 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_338370,RMVar_hsa_circ_79321,RMVar_hsa_circ_130872,RMVar_hsa_circ_130875,RMVar_hsa_circ_37958,RMVar_hsa_circ_297321,RMVar_hsa_circ_360311 9755 RMVar_ID_9755 Human_SNP_ID_7562231 A-to-I Human chr1 + 28570055 28570055 28570055 ACAAAAGGCGGGGTGCTGTGGCTCACGCCTGTAATCCCAACACTTTGGGAGGCTGAGTTGGGTGG ACAAAAGGCGGGGTGCTGTGGCTCACGCCTGTCATCCCAACACTTTGGGAGGCTGAGTTGGGTGG A C TRNAU1AP Ensembl:ENSG00000180098 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs569552208 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_338370,RMVar_hsa_circ_79321,RMVar_hsa_circ_130872,RMVar_hsa_circ_130875,RMVar_hsa_circ_37958,RMVar_hsa_circ_297321,RMVar_hsa_circ_360311 9756 RMVar_ID_9756 Human_SNP_ID_7562831 A-to-I Human chr1 + 28572385 28572384 28572386 CCAGCTAATTATTTTGTATTTTTAGTAGAGACAGGGTTTCTCCATGTTGGCTTGGCCGGTCTCAA CCAGCTAATTATTTTGTATTTTTAGTAGAGAC__GGTTTCTCCATGTTGGCTTGGCCGGTCTCAA CAG C TRNAU1AP Ensembl:ENSG00000180098 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1403801577 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_10918228 RMVar_hsa_circ_37958 9757 RMVar_ID_9757 Human_SNP_ID_7563392 A-to-I Human chr1 + 28574511 28574511 28574511 GGGAGGCTGAGGCAGGAGGATTGCTTGGGCCCAGGAGGTTGAGGCTTCAGTGAGCTGTGACTACA GGGAGGCTGAGGCAGGAGGATTGCTTGGGCCCGGGAGGTTGAGGCTTCAGTGAGCTGTGACTACA A G TRNAU1AP Ensembl:ENSG00000180098 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1304258046 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557067 RMVar_hsa_circ_37958 9758 RMVar_ID_9758 Human_SNP_ID_7568818 A-to-I Human chr1 + 28593413 28593413 28593413 TTTTCAGTAGAGACACGGGGTTTCACCGTGTTAGTCAGGATGGTCTGGATCTCCTGATCTCGTGA TTTTCAGTAGAGACACGGGGTTTCACCGTGTTCGTCAGGATGGTCTGGATCTCCTGATCTCGTGA A C RAB42 Ensembl:ENSG00000188060 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs953235219 Functional Loss SNV dbSNP153 33..33 33 - - - 9759 RMVar_ID_9759 Human_SNP_ID_7569582 A-to-I Human chr1 + 28596531 28596531 28596531 GTAATCCCAGCTACCGCGGAGTCTGAGGCAGGAGAATCACTGGAACCTGGGAGGCAGAGGCTGCA GTAATCCCAGCTACCGCGGAGTCTGAGGCAGGGGAATCACTGGAACCTGGGAGGCAGAGGCTGCA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs905292813 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18571231 9760 RMVar_ID_9760 Human_SNP_ID_7569589 A-to-I Human chr1 + 28596554 28596554 28596554 TGAGGCAGGAGAATCACTGGAACCTGGGAGGCAGAGGCTGCAGCGAGCTGACACCGTGCCACCGC TGAGGCAGGAGAATCACTGGAACCTGGGAGGCGGAGGCTGCAGCGAGCTGACACCGTGCCACCGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1438814095 Functional Loss SNV dbSNP153 33..33 33 - - - 9761 RMVar_ID_9761 Human_SNP_ID_7577754 A-to-I Human chr1 - 28628950 28628950 28628950 CTCCTGCCTCAGCCTCCCAAATAGCTGGGATTACAGGCGCCCGCCAACGCGCCTGGTTAATTTTG CTCCTGCCTCAGCCTCCCAAATAGCTGGGATTGCAGGCGCCCGCCAACGCGCCTGGTTAATTTTG T C TAF12 Ensembl:ENSG00000120656 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1217760242 Functional Loss SNV dbSNP153 33..33 33 - - - 9762 RMVar_ID_9762 Human_SNP_ID_7577886 A-to-I Human chr1 - 28629485 28629485 28629485 CTAATAATACAAAAAAATTAGCCAGGCGTGGTAGTACGTGCCTGTAATCCCAGATGCTCAGGCTG CTAATAATACAAAAAAATTAGCCAGGCGTGGTGGTACGTGCCTGTAATCCCAGATGCTCAGGCTG T C TAF12 Ensembl:ENSG00000120656 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971459946 Functional Loss SNV dbSNP153 33..33 33 - - - 9763 RMVar_ID_9763 Human_SNP_ID_7577887 A-to-I Human chr1 - 28629485 28629485 28629485 CTAATAATACAAAAAAATTAGCCAGGCGTGGTAGTACGTGCCTGTAATCCCAGATGCTCAGGCTG CTAATAATACAAAAAAATTAGCCAGGCGTGGTCGTACGTGCCTGTAATCCCAGATGCTCAGGCTG T G TAF12 Ensembl:ENSG00000120656 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971459946 Functional Loss SNV dbSNP153 33..33 33 - - - 9764 RMVar_ID_9764 Human_SNP_ID_7578023 A-to-I Human chr1 - 28630072 28630072 28630072 AGCTGGGCATGGTGGTGCATGCCTGTAGTTCCAGCTTCTGAGGAAGCTGAGGTGGGAGGATAGCT AGCTGGGCATGGTGGTGCATGCCTGTAGTTCCGGCTTCTGAGGAAGCTGAGGTGGGAGGATAGCT T C TAF12 Ensembl:ENSG00000120656 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs773495764 Functional Loss SNV dbSNP153 33..33 33 - - - 9765 RMVar_ID_9765 Human_SNP_ID_7579022 A-to-I Human chr1 - 28633790 28633790 28633790 CTCCTGCCTCAGCCTCCCGAATAGCTGGGATTACAGGCATGCACCACCATGCCCAGCTAATTTTT CTCCTGCCTCAGCCTCCCGAATAGCTGGGATTGCAGGCATGCACCACCATGCCCAGCTAATTTTT T C TAF12 Ensembl:ENSG00000120656 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs569430339 Functional Loss SNV dbSNP153 33..33 33 - - - 9766 RMVar_ID_9766 Human_SNP_ID_7579025 A-to-I Human chr1 - 28633800 28633800 28633800 TCTAGCGATTCTCCTGCCTCAGCCTCCCGAATAGCTGGGATTACAGGCATGCACCACCATGCCCA TCTAGCGATTCTCCTGCCTCAGCCTCCCGAATGGCTGGGATTACAGGCATGCACCACCATGCCCA T C TAF12 Ensembl:ENSG00000120656 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1456415140 Functional Loss SNV dbSNP153 33..33 33 - - - 9767 RMVar_ID_9767 Human_SNP_ID_7580114 A-to-I Human chr1 - 28637423 28637423 28637423 TGACCTCGTGATCCGCCTGCCTCGGCCTCCCAAAGTTCTAGGATTACAGGCGTGAGCCACTGTAC TGACCTCGTGATCCGCCTGCCTCGGCCTCCCAGAGTTCTAGGATTACAGGCGTGAGCCACTGTAC T C TAF12 Ensembl:ENSG00000120656 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1225718593 Functional Loss SNV dbSNP153 33..33 33 - - - 9768 RMVar_ID_9768 Human_SNP_ID_7580456 A-to-I Human chr1 - 28638602 28638602 28638602 GTGTGCTTATAATCCCGGCTACCTGGGAGGCTAAGGCAGGACAATCGCTGGAACCCGGGAGGCAG GTGTGCTTATAATCCCGGCTACCTGGGAGGCTGAGGCAGGACAATCGCTGGAACCCGGGAGGCAG T C TAF12 Ensembl:ENSG00000120656 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1303041376 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10918854 9769 RMVar_ID_9769 Human_SNP_ID_7581152 A-to-I Human chr1 - 28641311 28641311 28641311 GCCCGGCTACTTTTTGTATTTTTAGTAGAGACAGGTTTTTGCCATGTTGGCCAGGCTGTGTTTCG GCCCGGCTACTTTTTGTATTTTTAGTAGAGACCGGTTTTTGCCATGTTGGCCAGGCTGTGTTTCG T G TAF12 Ensembl:ENSG00000120656 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1289347471 Functional Loss SNV dbSNP153 33..33 33 - - - 9770 RMVar_ID_9770 Human_SNP_ID_7590028 A-to-I Human chr1 + 28671594 28671594 28671594 AAACCCCGTCTCTACAAAAAATGACAAAAATTAGATGGGCGTGGTGGAGCTAGTTGCCTGTGGTC AAACCCCGTCTCTACAAAAAATGACAAAAATTTGATGGGCGTGGTGGAGCTAGTTGCCTGTGGTC A T GMEB1 Ensembl:ENSG00000162419 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1263033157 Functional Loss SNV dbSNP153 33..33 33 - - - 9771 RMVar_ID_9771 Human_SNP_ID_7590117 A-to-I Human chr1 + 28671848 28671848 28671848 GGAATAAATAAATATTTTGGGCTGGGCGCGGTAGCTCACGCCTGTAATCCCAGCACTTTGGGAGG GGAATAAATAAATATTTTGGGCTGGGCGCGGTTGCTCACGCCTGTAATCCCAGCACTTTGGGAGG A T GMEB1 Ensembl:ENSG00000162419 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1203046703 Functional Loss SNV dbSNP153 33..33 33 - - - 9772 RMVar_ID_9772 Human_SNP_ID_7590708 A-to-I Human chr1 + 28673823 28673823 28673823 ATTGCTTGAGCCCAGGAGTTTGACACCAGGCTAGGCAACATAGCAAGACCTCATGTCTACAAAGA ATTGCTTGAGCCCAGGAGTTTGACACCAGGCTGGGCAACATAGCAAGACCTCATGTCTACAAAGA A G GMEB1 Ensembl:ENSG00000162419 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs555843034 Functional Loss SNV dbSNP153 33..33 33 - - - 9773 RMVar_ID_9773 Human_SNP_ID_7590711 A-to-I Human chr1 + 28673832 28673832 28673832 GCCCAGGAGTTTGACACCAGGCTAGGCAACATAGCAAGACCTCATGTCTACAAAGAAGTAAAGAA GCCCAGGAGTTTGACACCAGGCTAGGCAACATCGCAAGACCTCATGTCTACAAAGAAGTAAAGAA A C GMEB1 Ensembl:ENSG00000162419 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1015162677 Functional Loss SNV dbSNP153 33..33 33 - - - 9774 RMVar_ID_9774 Human_SNP_ID_7591626 A-to-I Human chr1 + 28676896 28676896 28676896 CAAGATGGTGAAACCCTGACTCTACTAAAAATACAAAAAGATTAGCTAGACATGGTGGCGGGCAC CAAGATGGTGAAACCCTGACTCTACTAAAAATTCAAAAAGATTAGCTAGACATGGTGGCGGGCAC A T GMEB1 Ensembl:ENSG00000162419 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1557496062 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8307513 9775 RMVar_ID_9775 Human_SNP_ID_7592625 A-to-I Human chr1 + 28680897 28680897 28680897 GAAACCCCATCTCTACTAAAAATATAAAAATTAGCTGGACATGGTGGGGCATGCCTGTAATCCCA GAAACCCCATCTCTACTAAAAATATAAAAATTTGCTGGACATGGTGGGGCATGCCTGTAATCCCA A T GMEB1 Ensembl:ENSG00000162419 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs997458150 Functional Loss SNV dbSNP153 33..33 33 - - - 9776 RMVar_ID_9776 Human_SNP_ID_7592720 A-to-I Human chr1 + 28681330 28681330 28681330 GCAGAGGTTGCAGTGAGCCAAGATCGTGCCACAGAACTCCAGTCTGGGCAACGGAGCGAGACCGC GCAGAGGTTGCAGTGAGCCAAGATCGTGCCACGGAACTCCAGTCTGGGCAACGGAGCGAGACCGC A G GMEB1 Ensembl:ENSG00000162419 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1442842553 Functional Loss SNV dbSNP153 33..33 33 - - - 9777 RMVar_ID_9777 Human_SNP_ID_7592982 A-to-I Human chr1 + 28682418 28682418 28682418 GAGACGGGTGGATCATTTGAGGTTAGGAGTTCAAGACCAGCCTGGCCAACACGGTGAAATCCCGT GAGACGGGTGGATCATTTGAGGTTAGGAGTTCCAGACCAGCCTGGCCAACACGGTGAAATCCCGT A C GMEB1 Ensembl:ENSG00000162419 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs981963330 Functional Loss SNV dbSNP153 33..33 33 - - - 9778 RMVar_ID_9778 Human_SNP_ID_7595057 A-to-I Human chr1 + 28689508 28689505 28689508 AAATTTAGTGGGGCGTGGTGGCGGGCTCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAATTTAGTGGGGCGTGGTGGCGGGCTCCT___GTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA TGTA T GMEB1 Ensembl:ENSG00000162419 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1245031235 Functional Loss DEL dbSNP153 31..33 33 - - - RMVar_hsa_circ_130888,RMVar_hsa_circ_293624,RMVar_hsa_circ_329397,RMVar_hsa_circ_331207,RMVar_hsa_circ_319348,RMVar_hsa_circ_329195,RMVar_hsa_circ_306719,RMVar_hsa_circ_130890,RMVar_hsa_circ_130891,RMVar_hsa_circ_130889,RMVar_hsa_circ_347709,RMVar_hsa_circ_368990,RMVar_hsa_circ_25773 9779 RMVar_ID_9779 Human_SNP_ID_7597739 A-to-I Human chr1 + 28698960 28698960 28698960 GAGCCGAGATCGTCCCATATTCCAGCCTGGGTAACAGAGCAAGACTCTGTCTCAAAAAAAAAGGA GAGCCGAGATCGTCCCATATTCCAGCCTGGGTGACAGAGCAAGACTCTGTCTCAAAAAAAAAGGA A G GMEB1 Ensembl:ENSG00000162419 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs886711389 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_329397,RMVar_hsa_circ_319348,RMVar_hsa_circ_329195,RMVar_hsa_circ_130890,RMVar_hsa_circ_130891,RMVar_hsa_circ_25773,RMVar_hsa_circ_280530,RMVar_hsa_circ_130892,RMVar_hsa_circ_295897,RMVar_hsa_circ_130893,RMVar_hsa_circ_365915,RMVar_hsa_circ_337257,RMVar_hsa_circ_130897,RMVar_hsa_circ_28247,RMVar_hsa_circ_364245 9780 RMVar_ID_9780 Human_SNP_ID_7597860 A-to-I Human chr1 + 28699485 28699485 28699485 AGAATCTTGCTTTGTCACCCGGGCTGGAGTGCAATGGTGCAATCTTGGCTCACTGCAACCTCCCC AGAATCTTGCTTTGTCACCCGGGCTGGAGTGCGATGGTGCAATCTTGGCTCACTGCAACCTCCCC A G GMEB1 Ensembl:ENSG00000162419 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs867030147 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_329397,RMVar_hsa_circ_319348,RMVar_hsa_circ_329195,RMVar_hsa_circ_130890,RMVar_hsa_circ_130891,RMVar_hsa_circ_25773,RMVar_hsa_circ_280530,RMVar_hsa_circ_130892,RMVar_hsa_circ_295897,RMVar_hsa_circ_130893,RMVar_hsa_circ_365915,RMVar_hsa_circ_337257,RMVar_hsa_circ_130897,RMVar_hsa_circ_28247,RMVar_hsa_circ_364245 9781 RMVar_ID_9781 Human_SNP_ID_7597879 A-to-I Human chr1 + 28699533 28699533 28699533 CTCACTGCAACCTCCCCCTCCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCGTGTAGTGAGA CTCACTGCAACCTCCCCCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGTGTAGTGAGA A G GMEB1 Ensembl:ENSG00000162419 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs879877530 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_329397,RMVar_hsa_circ_319348,RMVar_hsa_circ_329195,RMVar_hsa_circ_130890,RMVar_hsa_circ_130891,RMVar_hsa_circ_25773,RMVar_hsa_circ_280530,RMVar_hsa_circ_130892,RMVar_hsa_circ_295897,RMVar_hsa_circ_130893,RMVar_hsa_circ_365915,RMVar_hsa_circ_337257,RMVar_hsa_circ_130897,RMVar_hsa_circ_28247,RMVar_hsa_circ_364245 9782 RMVar_ID_9782 Human_SNP_ID_7598460 A-to-I Human chr1 + 28701760 28701760 28701760 CCAGCTAGTTTTTATAGAAACTGGGTTTTGCTATGTTGCCCAGGCTGGCCTCAGACTCCTGGACT CCAGCTAGTTTTTATAGAAACTGGGTTTTGCTGTGTTGCCCAGGCTGGCCTCAGACTCCTGGACT A G GMEB1 Ensembl:ENSG00000162419 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1374779593 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_329397,RMVar_hsa_circ_319348,RMVar_hsa_circ_329195,RMVar_hsa_circ_130890,RMVar_hsa_circ_130891,RMVar_hsa_circ_25773,RMVar_hsa_circ_280530,RMVar_hsa_circ_130892,RMVar_hsa_circ_295897,RMVar_hsa_circ_130893,RMVar_hsa_circ_365915,RMVar_hsa_circ_337257,RMVar_hsa_circ_130897,RMVar_hsa_circ_28247,RMVar_hsa_circ_364245 9783 RMVar_ID_9783 Human_SNP_ID_7602052 A-to-I Human chr1 + 28715349 28715349 28715349 AGCCGGGCGTGGTGGCTCACGCCTGCAATCCCAGCACTTTGGGAGGCCGAGGCGGGTGGATCACG AGCCGGGCGTGGTGGCTCACGCCTGCAATCCCCGCACTTTGGGAGGCCGAGGCGGGTGGATCACG A C GMEB1 Ensembl:ENSG00000162419 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs748545984 Functional Loss SNV dbSNP153 33..33 33 - - - 9784 RMVar_ID_9784 Human_SNP_ID_7602229 A-to-I Human chr1 + 28715952 28715952 28715952 CGTCTCTACTGAAAATACAAAAAAAAAAAATTAGCTGGGCATGGTGGCACGCGCCTGTAATCCCA CGTCTCTACTGAAAATACAAAAAAAAAAAATTGGCTGGGCATGGTGGCACGCGCCTGTAATCCCA A G GMEB1 Ensembl:ENSG00000162419 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1449996818 Functional Loss SNV dbSNP153 33..33 33 - - - 9785 RMVar_ID_9785 Human_SNP_ID_7602604 A-to-I Human chr1 + 28717470 28717470 28717470 CCTTGGCCTCCCAAAGTGTTGGGATTACAGGCATGAGCCACCGCACCCAGCCTGAAGGTGACTCT CCTTGGCCTCCCAAAGTGTTGGGATTACAGGCGTGAGCCACCGCACCCAGCCTGAAGGTGACTCT A G GMEB1 Ensembl:ENSG00000162419 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs888518013 Functional Loss SNV dbSNP153 33..33 33 - - - 9786 RMVar_ID_9786 Human_SNP_ID_7602794 A-to-I Human chr1 + 28718388 28718387 28718389 TTTCAGAAGCTGAGGCAGAATTGCTTGAGGCCAAGAGTTTAAGACTAGCCTGGTCAACATAGCCA TTTCAGAAGCTGAGGCAGAATTGCTTGAGGCC__GAGTTTAAGACTAGCCTGGTCAACATAGCCA CAA C GMEB1 Ensembl:ENSG00000162419 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1316113666 Functional Loss DEL dbSNP153 33..34 33 - - - 9787 RMVar_ID_9787 Human_SNP_ID_7602795 A-to-I Human chr1 + 28718388 28718388 28718388 TTTCAGAAGCTGAGGCAGAATTGCTTGAGGCCAAGAGTTTAAGACTAGCCTGGTCAACATAGCCA TTTCAGAAGCTGAGGCAGAATTGCTTGAGGCCCAGAGTTTAAGACTAGCCTGGTCAACATAGCCA A C GMEB1 Ensembl:ENSG00000162419 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1325685756 Functional Loss SNV dbSNP153 33..33 33 - - - 9788 RMVar_ID_9788 Human_SNP_ID_7602805 A-to-I Human chr1 + 28718416 28718416 28718416 GGCCAAGAGTTTAAGACTAGCCTGGTCAACATAGCCAGACCCCATCTCTATAAAAAAATGTAAAA GGCCAAGAGTTTAAGACTAGCCTGGTCAACATGGCCAGACCCCATCTCTATAAAAAAATGTAAAA A G GMEB1 Ensembl:ENSG00000162419 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037132511 Functional Loss SNV dbSNP153 33..33 33 - - - 9789 RMVar_ID_9789 Human_SNP_ID_7602806 A-to-I Human chr1 + 28718416 28718416 28718416 GGCCAAGAGTTTAAGACTAGCCTGGTCAACATAGCCAGACCCCATCTCTATAAAAAAATGTAAAA GGCCAAGAGTTTAAGACTAGCCTGGTCAACATTGCCAGACCCCATCTCTATAAAAAAATGTAAAA A T GMEB1 Ensembl:ENSG00000162419 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037132511 Functional Loss SNV dbSNP153 33..33 33 - - - 9790 RMVar_ID_9790 Human_SNP_ID_7603483 A-to-I Human chr1 + 28721205 28721205 28721205 CTCCGTCGCCCAGGCTGGAGTGCAGTGGTGTGATCTCGGCTCACTGCAAGCTCCACCTCCCGGGT CTCCGTCGCCCAGGCTGGAGTGCAGTGGTGTGTTCTCGGCTCACTGCAAGCTCCACCTCCCGGGT A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1224676592 Functional Loss SNV dbSNP153 33..33 33 - - - 9791 RMVar_ID_9791 Human_SNP_ID_7610325 A-to-I Human chr1 + 28744926 28744926 28744926 CCTGAGCTCAAGTGATCTGCCCCTGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACTGCAG CCTGAGCTCAAGTGATCTGCCCCTGCCTCCCATAGTGCTGGGATTACAGGTGTGAGCCACTGCAG A T YTHDF2 Ensembl:ENSG00000198492 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs940068448 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118074,RMVar_hsa_circ_88086,RMVar_hsa_circ_130902,RMVar_hsa_circ_130903 9792 RMVar_ID_9792 Human_SNP_ID_7612895 A-to-I Human chr1 + 28753441 28753441 28753441 GTGATGAGGCACACCTGTAGTCCTAGTTGCTCAGGAGGCTGAGACAGGAGGATTGCTTGAGCCCG GTGATGAGGCACACCTGTAGTCCTAGTTGCTCGGGAGGCTGAGACAGGAGGATTGCTTGAGCCCG A G YTHDF2 Ensembl:ENSG00000198492 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1261206749 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10920157 RMVar_hsa_circ_118074,RMVar_hsa_circ_88086,RMVar_hsa_circ_130902,RMVar_hsa_circ_130903 9793 RMVar_ID_9793 Human_SNP_ID_7613114 A-to-I Human chr1 + 28754272 28754272 28754272 CTATGAGGCTGGGTGAGTTGGCTCACGCCTCTAATTCCAGCACTTTGGGAGGCCAAGGTTGGCAG CTATGAGGCTGGGTGAGTTGGCTCACGCCTCTGATTCCAGCACTTTGGGAGGCCAAGGTTGGCAG A G YTHDF2 Ensembl:ENSG00000198492 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1439358142 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118074,RMVar_hsa_circ_88086,RMVar_hsa_circ_130902,RMVar_hsa_circ_130903 9794 RMVar_ID_9794 Human_SNP_ID_7616177 A-to-I Human chr1 + 28765500 28765500 28765500 CAGGCTAGAATGTAGCGGTGGCATCATAGCTCACTGTAACCTCTAACTCCTGGGTTCAAGCTGTC CAGGCTAGAATGTAGCGGTGGCATCATAGCTCTCTGTAACCTCTAACTCCTGGGTTCAAGCTGTC A T YTHDF2 Ensembl:ENSG00000198492 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1192210421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10920622 RMVar_hsa_circ_118074,RMVar_hsa_circ_88086,RMVar_hsa_circ_130902,RMVar_hsa_circ_130903 9795 RMVar_ID_9795 Human_SNP_ID_7616184 A-to-I Human chr1 + 28765525 28765525 28765525 ATAGCTCACTGTAACCTCTAACTCCTGGGTTCAAGCTGTCCTCCCACCTCAGCCTTCCAAGTAGC ATAGCTCACTGTAACCTCTAACTCCTGGGTTCGAGCTGTCCTCCCACCTCAGCCTTCCAAGTAGC A G YTHDF2 Ensembl:ENSG00000198492 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1039504687 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118074,RMVar_hsa_circ_88086,RMVar_hsa_circ_130902,RMVar_hsa_circ_130903 9796 RMVar_ID_9796 Human_SNP_ID_7647432 A-to-I Human chr1 + 28891962 28891962 28891962 ATACAAAAAATTAGCTGGGCATGGTTGGTGGCAGGCGTCTATAATCCCAGCTACTCGGGATGCTG ATACAAAAAATTAGCTGGGCATGGTTGGTGGCCGGCGTCTATAATCCCAGCTACTCGGGATGCTG A C EPB41 Ensembl:ENSG00000159023 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928793031 Functional Loss SNV dbSNP153 33..33 33 - - - 9797 RMVar_ID_9797 Human_SNP_ID_7647439 A-to-I Human chr1 + 28891982 28891982 28891982 ATGGTTGGTGGCAGGCGTCTATAATCCCAGCTACTCGGGATGCTGAGGCAGGAGAATCACTTGAA ATGGTTGGTGGCAGGCGTCTATAATCCCAGCTCCTCGGGATGCTGAGGCAGGAGAATCACTTGAA A C EPB41 Ensembl:ENSG00000159023 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs566590626 Functional Loss SNV dbSNP153 33..33 33 - - - 9798 RMVar_ID_9798 Human_SNP_ID_7647440 A-to-I Human chr1 + 28891982 28891982 28891982 ATGGTTGGTGGCAGGCGTCTATAATCCCAGCTACTCGGGATGCTGAGGCAGGAGAATCACTTGAA ATGGTTGGTGGCAGGCGTCTATAATCCCAGCTGCTCGGGATGCTGAGGCAGGAGAATCACTTGAA A G EPB41 Ensembl:ENSG00000159023 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs566590626 Functional Loss SNV dbSNP153 33..33 33 - - - 9799 RMVar_ID_9799 Human_SNP_ID_7647772 A-to-I Human chr1 + 28893271 28893271 28893271 TTTCATATTTTTTGTAGAGATGGGGTTTCCCCATGTTGCCTAGGCTGGTCTTGAACTCCTGAGCT TTTCATATTTTTTGTAGAGATGGGGTTTCCCCGTGTTGCCTAGGCTGGTCTTGAACTCCTGAGCT A G EPB41 Ensembl:ENSG00000159023 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1236396802 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557727 9800 RMVar_ID_9800 Human_SNP_ID_7651710 A-to-I Human chr1 + 28909679 28909679 28909679 AAAATTATCTGGGTGTGGTGGCATATACCTGTAGTCCCAGCTACTCAGGAGGCTGAGGAGGCAGG AAAATTATCTGGGTGTGGTGGCATATACCTGTGGTCCCAGCTACTCAGGAGGCTGAGGAGGCAGG A G EPB41 Ensembl:ENSG00000159023 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1375626184 Functional Loss SNV dbSNP153 33..33 33 - - - 9801 RMVar_ID_9801 Human_SNP_ID_7668742 A-to-I Human chr1 - 28982626 28982626 28982626 AAAACCATGATGGGCTTTTTGCTGTAGGCCCGAGTGGTTGCTGCCGAAATGGGCAAGTTCATGAA AAAACCATGATGGGCTTTTTGCTGTAGGCCCGTGTGGTTGCTGCCGAAATGGGCAAGTTCATGAA T A RF00017-1003 RNACentral:URS0000945854 SRP RNA intron GSE38233 cultured B-cells - 24183664 RNA-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 9802 RMVar_ID_9802 Human_SNP_ID_7668743 A-to-I Human chr1 - 28982626 28982626 28982626 AAAACCATGATGGGCTTTTTGCTGTAGGCCCGAGTGGTTGCTGCCGAAATGGGCAAGTTCATGAA AAAACCATGATGGGCTTTTTGCTGTAGGCCCGGGTGGTTGCTGCCGAAATGGGCAAGTTCATGAA T C RF00017-1003 RNACentral:URS0000945854 SRP RNA intron GSE38233 cultured B-cells - 24183664 RNA-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 9803 RMVar_ID_9803 Human_SNP_ID_7685415 A-to-I Human chr1 + 29055749 29055749 29055749 GGACGGGTGGATCACAGCCTGGCCAACATGGCAAAACCCCGTCTTTACTAAAAATACAAAAATTA GGACGGGTGGATCACAGCCTGGCCAACATGGCGAAACCCCGTCTTTACTAAAAATACAAAAATTA A G EPB41 Ensembl:ENSG00000159023 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1472403161 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123268,RMVar_hsa_circ_130905,RMVar_hsa_circ_313277,RMVar_hsa_circ_59593,RMVar_hsa_circ_62970,RMVar_hsa_circ_31453,RMVar_hsa_circ_313731,RMVar_hsa_circ_54704,RMVar_hsa_circ_65824,RMVar_hsa_circ_68426,RMVar_hsa_circ_313481,RMVar_hsa_circ_358156,RMVar_hsa_circ_346919,RMVar_hsa_circ_289678,RMVar_hsa_circ_130921,RMVar_hsa_circ_130922,RMVar_hsa_circ_130926,RMVar_hsa_circ_336566,RMVar_hsa_circ_3559,RMVar_hsa_circ_349340,RMVar_hsa_circ_75700,RMVar_hsa_circ_130928,RMVar_hsa_circ_41363,RMVar_hsa_circ_130927,RMVar_hsa_circ_26900,RMVar_hsa_circ_130925 9804 RMVar_ID_9804 Human_SNP_ID_7687798 A-to-I Human chr1 + 29065742 29065742 29065742 TCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGACAGGCAGATCACTTGAGTCCAGTAGTTTA TCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGACAGGCAGATCACTTGAGTCCAGTAGTTTA A G EPB41 Ensembl:ENSG00000159023 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs995049566 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_38298,Human_Splice_Rec_38299,Human_Splice_Rec_38356 RMVar_hsa_circ_123268,RMVar_hsa_circ_130905,RMVar_hsa_circ_59593,RMVar_hsa_circ_62970,RMVar_hsa_circ_54704,RMVar_hsa_circ_313481,RMVar_hsa_circ_358156,RMVar_hsa_circ_346919,RMVar_hsa_circ_130921,RMVar_hsa_circ_54234,RMVar_hsa_circ_130926,RMVar_hsa_circ_336566,RMVar_hsa_circ_75700,RMVar_hsa_circ_130928,RMVar_hsa_circ_41363,RMVar_hsa_circ_130927,RMVar_hsa_circ_346075,RMVar_hsa_circ_310663,RMVar_hsa_circ_34650 9805 RMVar_ID_9805 Human_SNP_ID_7688140 A-to-I Human chr1 + 29067097 29067097 29067097 GGTTCACAGGCCGGGCTTGGTGGCTCACACCTATAGTCCTAGCACTTTGGGAGGCTGAGGCGGGC GGTTCACAGGCCGGGCTTGGTGGCTCACACCTGTAGTCCTAGCACTTTGGGAGGCTGAGGCGGGC A G EPB41 Ensembl:ENSG00000159023 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027493696 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123268,RMVar_hsa_circ_130905,RMVar_hsa_circ_59593,RMVar_hsa_circ_62970,RMVar_hsa_circ_54704,RMVar_hsa_circ_313481,RMVar_hsa_circ_358156,RMVar_hsa_circ_346919,RMVar_hsa_circ_130921,RMVar_hsa_circ_54234,RMVar_hsa_circ_130926,RMVar_hsa_circ_336566,RMVar_hsa_circ_75700,RMVar_hsa_circ_130928,RMVar_hsa_circ_41363,RMVar_hsa_circ_130927,RMVar_hsa_circ_346075,RMVar_hsa_circ_310663,RMVar_hsa_circ_34650 9806 RMVar_ID_9806 Human_SNP_ID_7690514 A-to-I Human chr1 + 29078170 29078154 29078170 GAACCTGGGAGGCAGACATTGCAGTGAGCCAAAATTGCACCACTGCACTCCAGCCTGGGTGAAAG GAACCTGGGAGGCAGAC________________ATTGCACCACTGCACTCCAGCCTGGGTGAAAG CATTGCAGTGAGCCAAA C EPB41 Ensembl:ENSG00000159023 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1289282170 Functional Loss DEL dbSNP153 18..33 33 - - - Human_RBP_ID_24681436 RMVar_hsa_circ_123268,RMVar_hsa_circ_130905,RMVar_hsa_circ_59593,RMVar_hsa_circ_62970,RMVar_hsa_circ_54704,RMVar_hsa_circ_313481,RMVar_hsa_circ_358156,RMVar_hsa_circ_346919,RMVar_hsa_circ_130921,RMVar_hsa_circ_54234,RMVar_hsa_circ_130926,RMVar_hsa_circ_336566,RMVar_hsa_circ_75700,RMVar_hsa_circ_130928,RMVar_hsa_circ_41363,RMVar_hsa_circ_130927,RMVar_hsa_circ_346075,RMVar_hsa_circ_310663,RMVar_hsa_circ_34650 9807 RMVar_ID_9807 Human_SNP_ID_7690517 A-to-I Human chr1 + 29078168 29078167 29078168 CTGAACCTGGGAGGCAGACATTGCAGTGAGCCAAAATTGCACCACTGCACTCCAGCCTGGGTGAA CTGAACCTGGGAGGCAGACATTGCAGTGAGCC_AAATTGCACCACTGCACTCCAGCCTGGGTGAA CA C EPB41 Ensembl:ENSG00000159023 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1325140192 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_24681436 RMVar_hsa_circ_123268,RMVar_hsa_circ_130905,RMVar_hsa_circ_59593,RMVar_hsa_circ_62970,RMVar_hsa_circ_54704,RMVar_hsa_circ_313481,RMVar_hsa_circ_358156,RMVar_hsa_circ_346919,RMVar_hsa_circ_130921,RMVar_hsa_circ_54234,RMVar_hsa_circ_130926,RMVar_hsa_circ_336566,RMVar_hsa_circ_75700,RMVar_hsa_circ_130928,RMVar_hsa_circ_41363,RMVar_hsa_circ_130927,RMVar_hsa_circ_346075,RMVar_hsa_circ_310663,RMVar_hsa_circ_34650 9808 RMVar_ID_9808 Human_SNP_ID_7690617 A-to-I Human chr1 + 29078611 29078611 29078611 ACCCATCTCTACCAAAAAAAAATTAGCTGGGCATGATGGCATGCCTGTAGTCCCAGCTACACGGG ACCCATCTCTACCAAAAAAAAATTAGCTGGGCCTGATGGCATGCCTGTAGTCCCAGCTACACGGG A C EPB41 Ensembl:ENSG00000159023 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs958811937 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123268,RMVar_hsa_circ_130905,RMVar_hsa_circ_59593,RMVar_hsa_circ_62970,RMVar_hsa_circ_54704,RMVar_hsa_circ_313481,RMVar_hsa_circ_358156,RMVar_hsa_circ_346919,RMVar_hsa_circ_130921,RMVar_hsa_circ_54234,RMVar_hsa_circ_130926,RMVar_hsa_circ_336566,RMVar_hsa_circ_75700,RMVar_hsa_circ_130928,RMVar_hsa_circ_41363,RMVar_hsa_circ_130927,RMVar_hsa_circ_346075,RMVar_hsa_circ_310663,RMVar_hsa_circ_34650 9809 RMVar_ID_9809 Human_SNP_ID_7690620 A-to-I Human chr1 + 29078619 29078619 29078619 CTACCAAAAAAAAATTAGCTGGGCATGATGGCATGCCTGTAGTCCCAGCTACACGGGAGCCTGAG CTACCAAAAAAAAATTAGCTGGGCATGATGGCGTGCCTGTAGTCCCAGCTACACGGGAGCCTGAG A G EPB41 Ensembl:ENSG00000159023 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1453285689 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123268,RMVar_hsa_circ_130905,RMVar_hsa_circ_59593,RMVar_hsa_circ_62970,RMVar_hsa_circ_54704,RMVar_hsa_circ_313481,RMVar_hsa_circ_358156,RMVar_hsa_circ_346919,RMVar_hsa_circ_130921,RMVar_hsa_circ_54234,RMVar_hsa_circ_130926,RMVar_hsa_circ_336566,RMVar_hsa_circ_75700,RMVar_hsa_circ_130928,RMVar_hsa_circ_41363,RMVar_hsa_circ_130927,RMVar_hsa_circ_346075,RMVar_hsa_circ_310663,RMVar_hsa_circ_34650 9810 RMVar_ID_9810 Human_SNP_ID_7690750 A-to-I Human chr1 + 29079157 29079157 29079157 AGCTGGTATTACAGGCGCCTGCCACCACGCTCAGCTAATTTTTTGTATTTTTAGTAGAGATGGGG AGCTGGTATTACAGGCGCCTGCCACCACGCTCGGCTAATTTTTTGTATTTTTAGTAGAGATGGGG A G EPB41 Ensembl:ENSG00000159023 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs938914786 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123268,RMVar_hsa_circ_130905,RMVar_hsa_circ_59593,RMVar_hsa_circ_62970,RMVar_hsa_circ_54704,RMVar_hsa_circ_313481,RMVar_hsa_circ_358156,RMVar_hsa_circ_346919,RMVar_hsa_circ_130921,RMVar_hsa_circ_54234,RMVar_hsa_circ_130926,RMVar_hsa_circ_336566,RMVar_hsa_circ_75700,RMVar_hsa_circ_130928,RMVar_hsa_circ_41363,RMVar_hsa_circ_130927,RMVar_hsa_circ_346075,RMVar_hsa_circ_310663,RMVar_hsa_circ_34650 9811 RMVar_ID_9811 Human_SNP_ID_7690928 A-to-I Human chr1 + 29079886 29079886 29079886 AGGCATGATTGCGCGGGCCTGTAGTTCCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCTCCGC AGGCATGATTGCGCGGGCCTGTAGTTCCAGCTGCTCGGGAGGCTGAGGCAGGAGAATTGCTCCGC A G EPB41 Ensembl:ENSG00000159023 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1408354922 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123268,RMVar_hsa_circ_130905,RMVar_hsa_circ_59593,RMVar_hsa_circ_62970,RMVar_hsa_circ_54704,RMVar_hsa_circ_313481,RMVar_hsa_circ_358156,RMVar_hsa_circ_346919,RMVar_hsa_circ_130921,RMVar_hsa_circ_54234,RMVar_hsa_circ_130926,RMVar_hsa_circ_336566,RMVar_hsa_circ_75700,RMVar_hsa_circ_130928,RMVar_hsa_circ_41363,RMVar_hsa_circ_130927,RMVar_hsa_circ_346075,RMVar_hsa_circ_310663,RMVar_hsa_circ_34650 9812 RMVar_ID_9812 Human_SNP_ID_7690933 A-to-I Human chr1 + 29079903 29079903 29079903 CCTGTAGTTCCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCTCCGCCTGGGTGGCGGAGGTTG CCTGTAGTTCCAGCTACTCGGGAGGCTGAGGCCGGAGAATTGCTCCGCCTGGGTGGCGGAGGTTG A C EPB41 Ensembl:ENSG00000159023 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs890579336 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123268,RMVar_hsa_circ_130905,RMVar_hsa_circ_59593,RMVar_hsa_circ_62970,RMVar_hsa_circ_54704,RMVar_hsa_circ_313481,RMVar_hsa_circ_358156,RMVar_hsa_circ_346919,RMVar_hsa_circ_130921,RMVar_hsa_circ_54234,RMVar_hsa_circ_130926,RMVar_hsa_circ_336566,RMVar_hsa_circ_75700,RMVar_hsa_circ_130928,RMVar_hsa_circ_41363,RMVar_hsa_circ_130927,RMVar_hsa_circ_346075,RMVar_hsa_circ_310663,RMVar_hsa_circ_34650 9813 RMVar_ID_9813 Human_SNP_ID_7691083 A-to-I Human chr1 + 29080336 29080335 29080336 TTTGGCCAAGCTGGTCTTGAACTCTGGACCTCAAATGATCCGCCCACCTTGGCCTCCCAAAGTGC TTTGGCCAAGCTGGTCTTGAACTCTGGACCTC_AATGATCCGCCCACCTTGGCCTCCCAAAGTGC CA C EPB41 Ensembl:ENSG00000159023 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1196446745 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_123268,RMVar_hsa_circ_130905,RMVar_hsa_circ_59593,RMVar_hsa_circ_62970,RMVar_hsa_circ_54704,RMVar_hsa_circ_313481,RMVar_hsa_circ_358156,RMVar_hsa_circ_346919,RMVar_hsa_circ_130921,RMVar_hsa_circ_54234,RMVar_hsa_circ_130926,RMVar_hsa_circ_336566,RMVar_hsa_circ_75700,RMVar_hsa_circ_130928,RMVar_hsa_circ_41363,RMVar_hsa_circ_130927,RMVar_hsa_circ_346075,RMVar_hsa_circ_310663,RMVar_hsa_circ_34650 9814 RMVar_ID_9814 Human_SNP_ID_7691495 A-to-I Human chr1 + 29082144 29082143 29082144 TTGGGTTTTTTGTTTGTTTTGTTTCGTTTTTGAGACGGAGTCTCACTCTGTCACCCCGGCTGGAG TTGGGTTTTTTGTTTGTTTTGTTTCGTTTTTG_GACGGAGTCTCACTCTGTCACCCCGGCTGGAG GA G EPB41 Ensembl:ENSG00000159023 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1020205064 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_10922341 RMVar_hsa_circ_123268,RMVar_hsa_circ_130905,RMVar_hsa_circ_59593,RMVar_hsa_circ_62970,RMVar_hsa_circ_54704,RMVar_hsa_circ_313481,RMVar_hsa_circ_358156,RMVar_hsa_circ_346919,RMVar_hsa_circ_130921,RMVar_hsa_circ_54234,RMVar_hsa_circ_130926,RMVar_hsa_circ_336566,RMVar_hsa_circ_75700,RMVar_hsa_circ_130928,RMVar_hsa_circ_41363,RMVar_hsa_circ_130927,RMVar_hsa_circ_346075,RMVar_hsa_circ_310663,RMVar_hsa_circ_34650 9815 RMVar_ID_9815 Human_SNP_ID_7694465 A-to-I Human chr1 + 29095589 29095589 29095589 GGCCAGGAGTTTGAGATCAACCTGGACTACATAGTGAGACCCTGTTTCTCCAAAACATGTAAAAC GGCCAGGAGTTTGAGATCAACCTGGACTACATGGTGAGACCCTGTTTCTCCAAAACATGTAAAAC A G EPB41 Ensembl:ENSG00000159023 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1258317379 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123268,RMVar_hsa_circ_130905,RMVar_hsa_circ_59593,RMVar_hsa_circ_62970,RMVar_hsa_circ_54704,RMVar_hsa_circ_313481,RMVar_hsa_circ_358156,RMVar_hsa_circ_346919,RMVar_hsa_circ_130921,RMVar_hsa_circ_54234,RMVar_hsa_circ_130926,RMVar_hsa_circ_336566,RMVar_hsa_circ_75700,RMVar_hsa_circ_130928,RMVar_hsa_circ_41363,RMVar_hsa_circ_130927,RMVar_hsa_circ_346075,RMVar_hsa_circ_310663,RMVar_hsa_circ_34650 9816 RMVar_ID_9816 Human_SNP_ID_7695221 A-to-I Human chr1 + 29099130 29099128 29099130 GGAGTTCAGGACCGGCCTGGCCAACGTGGTGAAACCCCATCTCTACTAAAAATACAAAAATTCGC GGAGTTCAGGACCGGCCTGGCCAACGTGGTG__ACCCCATCTCTACTAAAAATACAAAAATTCGC GAA G EPB41 Ensembl:ENSG00000159023 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1456576384 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_123268,RMVar_hsa_circ_130905,RMVar_hsa_circ_62970,RMVar_hsa_circ_358156,RMVar_hsa_circ_346919,RMVar_hsa_circ_75700,RMVar_hsa_circ_130928,RMVar_hsa_circ_41363,RMVar_hsa_circ_130927,RMVar_hsa_circ_34650,RMVar_hsa_circ_7827,RMVar_hsa_circ_316698,RMVar_hsa_circ_280300,RMVar_hsa_circ_130931 9817 RMVar_ID_9817 Human_SNP_ID_7695223 A-to-I Human chr1 + 29099130 29099130 29099130 GGAGTTCAGGACCGGCCTGGCCAACGTGGTGAAACCCCATCTCTACTAAAAATACAAAAATTCGC GGAGTTCAGGACCGGCCTGGCCAACGTGGTGAGACCCCATCTCTACTAAAAATACAAAAATTCGC A G EPB41 Ensembl:ENSG00000159023 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1323114418 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123268,RMVar_hsa_circ_130905,RMVar_hsa_circ_62970,RMVar_hsa_circ_358156,RMVar_hsa_circ_346919,RMVar_hsa_circ_75700,RMVar_hsa_circ_130928,RMVar_hsa_circ_41363,RMVar_hsa_circ_130927,RMVar_hsa_circ_34650,RMVar_hsa_circ_7827,RMVar_hsa_circ_316698,RMVar_hsa_circ_280300,RMVar_hsa_circ_130931 9818 RMVar_ID_9818 Human_SNP_ID_7710342 A-to-I Human chr1 - 29153873 29153873 29153873 TCAGAGGCCGGGCACAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGCAGA TCAGAGGCCGGGCACAGTGGCTCACGCCTGTAGTCCCAGCACTTTGGGAGGCCAAGGCGGGCAGA T C SRSF4 Ensembl:ENSG00000116350 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1022832403 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70880,RMVar_hsa_circ_130936,RMVar_hsa_circ_130935,RMVar_hsa_circ_338632,RMVar_hsa_circ_130938 9819 RMVar_ID_9819 Human_SNP_ID_7710385 A-to-I Human chr1 - 29153989 29153989 29153989 AGGAGGCTGAGGCATGGGAATCGCTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCCGAGATCGCA AGGAGGCTGAGGCATGGGAATCGCTTGAACCCTGGAGGCAGAGGTTGCAGTGAGCCGAGATCGCA T A SRSF4 Ensembl:ENSG00000116350 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1405974519 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70880,RMVar_hsa_circ_130936,RMVar_hsa_circ_130935,RMVar_hsa_circ_338632,RMVar_hsa_circ_130938 9820 RMVar_ID_9820 Human_SNP_ID_7710386 A-to-I Human chr1 - 29153989 29153989 29153989 AGGAGGCTGAGGCATGGGAATCGCTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCCGAGATCGCA AGGAGGCTGAGGCATGGGAATCGCTTGAACCCGGGAGGCAGAGGTTGCAGTGAGCCGAGATCGCA T C SRSF4 Ensembl:ENSG00000116350 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1405974519 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70880,RMVar_hsa_circ_130936,RMVar_hsa_circ_130935,RMVar_hsa_circ_338632,RMVar_hsa_circ_130938 9821 RMVar_ID_9821 Human_SNP_ID_7710468 A-to-I Human chr1 - 29154205 29154205 29154205 ACAAAATTTAGTTGGGCGTGGTGGGTGCCTATAATCCCAGTGACTCGGGAGGCGGAGGCAGAAAA ACAAAATTTAGTTGGGCGTGGTGGGTGCCTATGATCCCAGTGACTCGGGAGGCGGAGGCAGAAAA T C SRSF4 Ensembl:ENSG00000116350 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs910931630 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70880,RMVar_hsa_circ_130936,RMVar_hsa_circ_130935,RMVar_hsa_circ_338632,RMVar_hsa_circ_130938 9822 RMVar_ID_9822 Human_SNP_ID_7710469 A-to-I Human chr1 - 29154207 29154207 29154207 TAACAAAATTTAGTTGGGCGTGGTGGGTGCCTATAATCCCAGTGACTCGGGAGGCGGAGGCAGAA TAACAAAATTTAGTTGGGCGTGGTGGGTGCCTGTAATCCCAGTGACTCGGGAGGCGGAGGCAGAA T C SRSF4 Ensembl:ENSG00000116350 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs943797014 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24763689 RMVar_hsa_circ_70880,RMVar_hsa_circ_130936,RMVar_hsa_circ_130935,RMVar_hsa_circ_338632,RMVar_hsa_circ_130938 9823 RMVar_ID_9823 Human_SNP_ID_7710740 A-to-I Human chr1 - 29155213 29155213 29155213 TTGTCAAGGCTGGTCTTGAATTCCTGGGATCAAGCAATCCTCCCGCCTCAGCTTGTCAAAGTGCT TTGTCAAGGCTGGTCTTGAATTCCTGGGATCACGCAATCCTCCCGCCTCAGCTTGTCAAAGTGCT T G SRSF4 Ensembl:ENSG00000116350 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388242609 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8444,RMVar_hsa_circ_70880,RMVar_hsa_circ_130935,RMVar_hsa_circ_290932,RMVar_hsa_circ_94503,RMVar_hsa_circ_130940,RMVar_hsa_circ_130941 9824 RMVar_ID_9824 Human_SNP_ID_7710848 A-to-I Human chr1 - 29155595 29155595 29155595 TCCAGCTGTTGGGGAGGCTGAGGCACAGAATCACTTGAACCTGGGAGGCAGAGGTTGCAGTGAGC TCCAGCTGTTGGGGAGGCTGAGGCACAGAATCTCTTGAACCTGGGAGGCAGAGGTTGCAGTGAGC T A SRSF4 Ensembl:ENSG00000116350 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1217919415 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10922938 RMVar_hsa_circ_8444,RMVar_hsa_circ_70880,RMVar_hsa_circ_130935,RMVar_hsa_circ_290932,RMVar_hsa_circ_94503,RMVar_hsa_circ_130940,RMVar_hsa_circ_130941 9825 RMVar_ID_9825 Human_SNP_ID_7710855 A-to-I Human chr1 - 29155630 29155630 29155630 AAAATCAGCTGGGTATGGTGGCGCGGACCTGCAGTTCCAGCTGTTGGGGAGGCTGAGGCACAGAA AAAATCAGCTGGGTATGGTGGCGCGGACCTGCGGTTCCAGCTGTTGGGGAGGCTGAGGCACAGAA T C SRSF4 Ensembl:ENSG00000116350 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1182849896 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10922938 RMVar_hsa_circ_8444,RMVar_hsa_circ_70880,RMVar_hsa_circ_130935,RMVar_hsa_circ_290932,RMVar_hsa_circ_94503,RMVar_hsa_circ_130940,RMVar_hsa_circ_130941 9826 RMVar_ID_9826 Human_SNP_ID_7710863 A-to-I Human chr1 - 29155648 29155648 29155648 TCTCTAATGAAAACACAAAAAATCAGCTGGGTATGGTGGCGCGGACCTGCAGTTCCAGCTGTTGG TCTCTAATGAAAACACAAAAAATCAGCTGGGTGTGGTGGCGCGGACCTGCAGTTCCAGCTGTTGG T C SRSF4 Ensembl:ENSG00000116350 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1466723217 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8444,RMVar_hsa_circ_70880,RMVar_hsa_circ_130935,RMVar_hsa_circ_290932,RMVar_hsa_circ_94503,RMVar_hsa_circ_130940,RMVar_hsa_circ_130941 9827 RMVar_ID_9827 Human_SNP_ID_7710892 A-to-I Human chr1 - 29155768 29155768 29155768 AGAAAATGGGCTGGGCACAGTGACCCATGCCTATAATCCTAGCACTTTGGGAGGCTGAGGCAGGT AGAAAATGGGCTGGGCACAGTGACCCATGCCTGTAATCCTAGCACTTTGGGAGGCTGAGGCAGGT T C SRSF4 Ensembl:ENSG00000116350 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs12041081 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11207906 RMVar_hsa_circ_8444,RMVar_hsa_circ_70880,RMVar_hsa_circ_130935,RMVar_hsa_circ_290932,RMVar_hsa_circ_94503,RMVar_hsa_circ_130940,RMVar_hsa_circ_130941 9828 RMVar_ID_9828 Human_SNP_ID_7711033 A-to-I Human chr1 - 29156297 29156297 29156297 CTGGGCTAGAATGCAGTGGCACAATCTCGCTCACTGCAACTTCCACCTCCTGGGTTCAAGCGATT CTGGGCTAGAATGCAGTGGCACAATCTCGCTCGCTGCAACTTCCACCTCCTGGGTTCAAGCGATT T C SRSF4 Ensembl:ENSG00000116350 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1308344044 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10922967 RMVar_hsa_circ_8444,RMVar_hsa_circ_70880,RMVar_hsa_circ_130935,RMVar_hsa_circ_290932,RMVar_hsa_circ_94503,RMVar_hsa_circ_130940,RMVar_hsa_circ_130941 9829 RMVar_ID_9829 Human_SNP_ID_7711626 A-to-I Human chr1 - 29158594 29158594 29158594 ACCCTGTCTCTACTTAAAAAGATACAAAAATTAGCCGGGCGTGGTGGTGGGCACCTGTAGTCCCA ACCCTGTCTCTACTTAAAAAGATACAAAAATTTGCCGGGCGTGGTGGTGGGCACCTGTAGTCCCA T A SRSF4 Ensembl:ENSG00000116350 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs989236635 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1153959,Human_RBP_ID_24681690 RMVar_hsa_circ_8444,RMVar_hsa_circ_70880,RMVar_hsa_circ_130935,RMVar_hsa_circ_290932,RMVar_hsa_circ_94503,RMVar_hsa_circ_130940,RMVar_hsa_circ_130941 9830 RMVar_ID_9830 Human_SNP_ID_7711627 A-to-I Human chr1 - 29158594 29158594 29158594 ACCCTGTCTCTACTTAAAAAGATACAAAAATTAGCCGGGCGTGGTGGTGGGCACCTGTAGTCCCA ACCCTGTCTCTACTTAAAAAGATACAAAAATTCGCCGGGCGTGGTGGTGGGCACCTGTAGTCCCA T G SRSF4 Ensembl:ENSG00000116350 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs989236635 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1153959,Human_RBP_ID_24681690 RMVar_hsa_circ_8444,RMVar_hsa_circ_70880,RMVar_hsa_circ_130935,RMVar_hsa_circ_290932,RMVar_hsa_circ_94503,RMVar_hsa_circ_130940,RMVar_hsa_circ_130941 9831 RMVar_ID_9831 Human_SNP_ID_7714943 A-to-I Human chr1 - 29172429 29172429 29172429 AAATTAGCTGGGCATGGTGGTAGGCTCCTGCAATCCTAGCTACTCGGGAGGCTGAGGCAGGAGAA AAATTAGCTGGGCATGGTGGTAGGCTCCTGCATTCCTAGCTACTCGGGAGGCTGAGGCAGGAGAA T A SRSF4 Ensembl:ENSG00000116350 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs571402989 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10923757 RMVar_hsa_circ_122894,RMVar_hsa_circ_130943 9832 RMVar_ID_9832 Human_SNP_ID_7714944 A-to-I Human chr1 - 29172429 29172429 29172429 AAATTAGCTGGGCATGGTGGTAGGCTCCTGCAATCCTAGCTACTCGGGAGGCTGAGGCAGGAGAA AAATTAGCTGGGCATGGTGGTAGGCTCCTGCAGTCCTAGCTACTCGGGAGGCTGAGGCAGGAGAA T C SRSF4 Ensembl:ENSG00000116350 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs571402989 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10923757 RMVar_hsa_circ_122894,RMVar_hsa_circ_130943 9833 RMVar_ID_9833 Human_SNP_ID_7714987 A-to-I Human chr1 - 29172587 29172587 29172587 AGCATGGAGTACCCCTGTTGTGTTTGCTGGCCAGGCGTGGTGGCTCACGTCTGTAATTCCAGCAC AGCATGGAGTACCCCTGTTGTGTTTGCTGGCCGGGCGTGGTGGCTCACGTCTGTAATTCCAGCAC T C SRSF4 Ensembl:ENSG00000116350 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs576370833 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_740958,Human_RBP_ID_5807514,Human_RBP_ID_10923771 RMVar_hsa_circ_122894,RMVar_hsa_circ_130943 9834 RMVar_ID_9834 Human_SNP_ID_7715219 A-to-I Human chr1 - 29173252 29173252 29173252 GCGCCTGTAGTCCCAGCTACTTGGGAGGTTGAAGTAGGAGAATGGCGTGAACCCGGGAGGCTGAG GCGCCTGTAGTCCCAGCTACTTGGGAGGTTGAGGTAGGAGAATGGCGTGAACCCGGGAGGCTGAG T C SRSF4 Ensembl:ENSG00000116350 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs989662385 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_96142,Human_RBP_ID_10923813 RMVar_hsa_circ_122894,RMVar_hsa_circ_130943 9835 RMVar_ID_9835 Human_SNP_ID_7715386 A-to-I Human chr1 - 29173578 29173578 29173578 TGGGTATGGTGGCACTTGCTGTAATCCCAGCTACTTAGGAGGCTGAGGCAGGAGAATCGCTAGAA TGGGTATGGTGGCACTTGCTGTAATCCCAGCTGCTTAGGAGGCTGAGGCAGGAGAATCGCTAGAA T C SRSF4 Ensembl:ENSG00000116350 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1268689342 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10923823 RMVar_hsa_circ_122894,RMVar_hsa_circ_130943 9836 RMVar_ID_9836 Human_SNP_ID_7715392 A-to-I Human chr1 - 29173605 29173605 29173605 GTCTGTACTAAAAAGACAAAAATTAGCTGGGTATGGTGGCACTTGCTGTAATCCCAGCTACTTAG GTCTGTACTAAAAAGACAAAAATTAGCTGGGTGTGGTGGCACTTGCTGTAATCCCAGCTACTTAG T C SRSF4 Ensembl:ENSG00000116350 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1241800160 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5807527 RMVar_hsa_circ_122894,RMVar_hsa_circ_130943 9837 RMVar_ID_9837 Human_SNP_ID_7715396 A-to-I Human chr1 - 29173628 29173628 29173628 CCTGGCCAGCATGGTGAAACCCCGTCTGTACTAAAAAGACAAAAATTAGCTGGGTATGGTGGCAC CCTGGCCAGCATGGTGAAACCCCGTCTGTACTGAAAAGACAAAAATTAGCTGGGTATGGTGGCAC T C SRSF4 Ensembl:ENSG00000116350 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1248047178 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122894,RMVar_hsa_circ_130943 9838 RMVar_ID_9838 Human_SNP_ID_7715525 A-to-I Human chr1 - 29174103 29174103 29174103 CTCACTGCAACCTCTGCCTCCCGGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCCAAGTAGCTGGG CTCACTGCAACCTCTGCCTCCCGGGTTCAAGCGGTTCTCCTGCCTCAGCCTCCCAAGTAGCTGGG T C SRSF4 Ensembl:ENSG00000116350 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs113632925 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_96143 RMVar_hsa_circ_122894,RMVar_hsa_circ_130943 9839 RMVar_ID_9839 Human_SNP_ID_7715543 A-to-I Human chr1 - 29174179 29174179 29174179 TTTTTTCTTTTTTTTTTTGAGATGGGGTCTCAATCTGTCTCCCAGGCTGCAGTGCAGTGCAGTGG TTTTTTCTTTTTTTTTTTGAGATGGGGTCTCAGTCTGTCTCCCAGGCTGCAGTGCAGTGCAGTGG T C SRSF4 Ensembl:ENSG00000116350 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs928745930 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_96143,Human_RBP_ID_5807531,Human_RBP_ID_10923843,Human_RBP_ID_17557068 RMVar_hsa_circ_122894,RMVar_hsa_circ_130943 9840 RMVar_ID_9840 Human_SNP_ID_7715587 A-to-I Human chr1 - 29174303 29174303 29174303 CAAGTAGACTTTGGGAGTCAAAGCATATACACATTTTAATGCTTTTGCTAGCTATTCCATTACTC CAAGTAGACTTTGGGAGTCAAAGCATATACACTTTTTAATGCTTTTGCTAGCTATTCCATTACTC T A SRSF4 Ensembl:ENSG00000116350 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2428558 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10923847,Human_RBP_ID_24359638 GWAS_ID_685,GWAS_ID_686,GWAS_ID_687,GWAS_ID_688,GWAS_ID_689,GWAS_ID_690,GWAS_ID_691,GWAS_ID_692,GWAS_ID_693,GWAS_ID_694,GWAS_ID_695,GWAS_ID_696,GWAS_ID_697,GWAS_ID_698,GWAS_ID_699,GWAS_ID_700,GWAS_ID_701,GWAS_ID_702,GWAS_ID_703,GWAS_ID_704,GWAS_ID_705,GWAS_ID_706,GWAS_ID_707,GWAS_ID_708,GWAS_ID_709,GWAS_ID_710,GWAS_ID_711,GWAS_ID_712,GWAS_ID_713,GWAS_ID_714,GWAS_ID_715,GWAS_ID_716,GWAS_ID_717,GWAS_ID_718,GWAS_ID_719,GWAS_ID_720,GWAS_ID_721,GWAS_ID_722,GWAS_ID_723,GWAS_ID_724,GWAS_ID_725,GWAS_ID_726,GWAS_ID_727,GWAS_ID_728,GWAS_ID_729,GWAS_ID_730,GWAS_ID_731,GWAS_ID_732,GWAS_ID_733,GWAS_ID_734,GWAS_ID_735,GWAS_ID_736,GWAS_ID_737,GWAS_ID_738,GWAS_ID_739,GWAS_ID_740,GWAS_ID_741,GWAS_ID_742,GWAS_ID_743,GWAS_ID_744,GWAS_ID_745,GWAS_ID_746,GWAS_ID_747,GWAS_ID_748,GWAS_ID_749,GWAS_ID_750,GWAS_ID_751,GWAS_ID_752,GWAS_ID_753,GWAS_ID_754,GWAS_ID_755,GWAS_ID_756,GWAS_ID_757,GWAS_ID_758,GWAS_ID_759,GWAS_ID_760,GWAS_ID_761,GWAS_ID_762,GWAS_ID_763,GWAS_ID_764,GWAS_ID_765,GWAS_ID_766,GWAS_ID_767,GWAS_ID_768,GWAS_ID_769,GWAS_ID_770,GWAS_ID_771,GWAS_ID_772,GWAS_ID_773,GWAS_ID_774,GWAS_ID_775,GWAS_ID_776,GWAS_ID_777,GWAS_ID_778,GWAS_ID_779,GWAS_ID_780,GWAS_ID_781,GWAS_ID_782,GWAS_ID_783,GWAS_ID_784 RMVar_hsa_circ_122894,RMVar_hsa_circ_130943 9841 RMVar_ID_9841 Human_SNP_ID_7715588 A-to-I Human chr1 - 29174303 29174303 29174303 CAAGTAGACTTTGGGAGTCAAAGCATATACACATTTTAATGCTTTTGCTAGCTATTCCATTACTC CAAGTAGACTTTGGGAGTCAAAGCATATACACGTTTTAATGCTTTTGCTAGCTATTCCATTACTC T C SRSF4 Ensembl:ENSG00000116350 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2428558 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10923847,Human_RBP_ID_24359638 GWAS_ID_685,GWAS_ID_686,GWAS_ID_687,GWAS_ID_688,GWAS_ID_689,GWAS_ID_690,GWAS_ID_691,GWAS_ID_692,GWAS_ID_693,GWAS_ID_694,GWAS_ID_695,GWAS_ID_696,GWAS_ID_697,GWAS_ID_698,GWAS_ID_699,GWAS_ID_700,GWAS_ID_701,GWAS_ID_702,GWAS_ID_703,GWAS_ID_704,GWAS_ID_705,GWAS_ID_706,GWAS_ID_707,GWAS_ID_708,GWAS_ID_709,GWAS_ID_710,GWAS_ID_711,GWAS_ID_712,GWAS_ID_713,GWAS_ID_714,GWAS_ID_715,GWAS_ID_716,GWAS_ID_717,GWAS_ID_718,GWAS_ID_719,GWAS_ID_720,GWAS_ID_721,GWAS_ID_722,GWAS_ID_723,GWAS_ID_724,GWAS_ID_725,GWAS_ID_726,GWAS_ID_727,GWAS_ID_728,GWAS_ID_729,GWAS_ID_730,GWAS_ID_731,GWAS_ID_732,GWAS_ID_733,GWAS_ID_734,GWAS_ID_735,GWAS_ID_736,GWAS_ID_737,GWAS_ID_738,GWAS_ID_739,GWAS_ID_740,GWAS_ID_741,GWAS_ID_742,GWAS_ID_743,GWAS_ID_744,GWAS_ID_745,GWAS_ID_746,GWAS_ID_747,GWAS_ID_748,GWAS_ID_749,GWAS_ID_750,GWAS_ID_751,GWAS_ID_752,GWAS_ID_753,GWAS_ID_754,GWAS_ID_755,GWAS_ID_756,GWAS_ID_757,GWAS_ID_758,GWAS_ID_759,GWAS_ID_760,GWAS_ID_761,GWAS_ID_762,GWAS_ID_763,GWAS_ID_764,GWAS_ID_765,GWAS_ID_766,GWAS_ID_767,GWAS_ID_768,GWAS_ID_769,GWAS_ID_770,GWAS_ID_771,GWAS_ID_772,GWAS_ID_773,GWAS_ID_774,GWAS_ID_775,GWAS_ID_776,GWAS_ID_777,GWAS_ID_778,GWAS_ID_779,GWAS_ID_780,GWAS_ID_781,GWAS_ID_782,GWAS_ID_783,GWAS_ID_784 RMVar_hsa_circ_122894,RMVar_hsa_circ_130943 9842 RMVar_ID_9842 Human_SNP_ID_7715589 A-to-I Human chr1 - 29174303 29174303 29174303 CAAGTAGACTTTGGGAGTCAAAGCATATACACATTTTAATGCTTTTGCTAGCTATTCCATTACTC CAAGTAGACTTTGGGAGTCAAAGCATATACACCTTTTAATGCTTTTGCTAGCTATTCCATTACTC T G SRSF4 Ensembl:ENSG00000116350 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2428558 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10923847,Human_RBP_ID_24359638 GWAS_ID_685,GWAS_ID_686,GWAS_ID_687,GWAS_ID_688,GWAS_ID_689,GWAS_ID_690,GWAS_ID_691,GWAS_ID_692,GWAS_ID_693,GWAS_ID_694,GWAS_ID_695,GWAS_ID_696,GWAS_ID_697,GWAS_ID_698,GWAS_ID_699,GWAS_ID_700,GWAS_ID_701,GWAS_ID_702,GWAS_ID_703,GWAS_ID_704,GWAS_ID_705,GWAS_ID_706,GWAS_ID_707,GWAS_ID_708,GWAS_ID_709,GWAS_ID_710,GWAS_ID_711,GWAS_ID_712,GWAS_ID_713,GWAS_ID_714,GWAS_ID_715,GWAS_ID_716,GWAS_ID_717,GWAS_ID_718,GWAS_ID_719,GWAS_ID_720,GWAS_ID_721,GWAS_ID_722,GWAS_ID_723,GWAS_ID_724,GWAS_ID_725,GWAS_ID_726,GWAS_ID_727,GWAS_ID_728,GWAS_ID_729,GWAS_ID_730,GWAS_ID_731,GWAS_ID_732,GWAS_ID_733,GWAS_ID_734,GWAS_ID_735,GWAS_ID_736,GWAS_ID_737,GWAS_ID_738,GWAS_ID_739,GWAS_ID_740,GWAS_ID_741,GWAS_ID_742,GWAS_ID_743,GWAS_ID_744,GWAS_ID_745,GWAS_ID_746,GWAS_ID_747,GWAS_ID_748,GWAS_ID_749,GWAS_ID_750,GWAS_ID_751,GWAS_ID_752,GWAS_ID_753,GWAS_ID_754,GWAS_ID_755,GWAS_ID_756,GWAS_ID_757,GWAS_ID_758,GWAS_ID_759,GWAS_ID_760,GWAS_ID_761,GWAS_ID_762,GWAS_ID_763,GWAS_ID_764,GWAS_ID_765,GWAS_ID_766,GWAS_ID_767,GWAS_ID_768,GWAS_ID_769,GWAS_ID_770,GWAS_ID_771,GWAS_ID_772,GWAS_ID_773,GWAS_ID_774,GWAS_ID_775,GWAS_ID_776,GWAS_ID_777,GWAS_ID_778,GWAS_ID_779,GWAS_ID_780,GWAS_ID_781,GWAS_ID_782,GWAS_ID_783,GWAS_ID_784 RMVar_hsa_circ_122894,RMVar_hsa_circ_130943 9843 RMVar_ID_9843 Human_SNP_ID_7715896 A-to-I Human chr1 - 29175291 29175291 29175291 CTGCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGTGTGCACCACCACCCCCGGCTAATTTTT CTGCTGCCTCAGCCTCCCAAGTAGCTGGGATTGCAGGTGTGCACCACCACCCCCGGCTAATTTTT T C SRSF4 Ensembl:ENSG00000116350 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1000693298 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122894,RMVar_hsa_circ_130943 9844 RMVar_ID_9844 Human_SNP_ID_7715915 A-to-I Human chr1 - 29175367 29175367 29175367 AGATGGAGTCTCTGTCTGTTGCCCAGGCTGGAATGCAGTGGCACAATCGTGGCTCACCTCCCAGG AGATGGAGTCTCTGTCTGTTGCCCAGGCTGGAGTGCAGTGGCACAATCGTGGCTCACCTCCCAGG T C SRSF4 Ensembl:ENSG00000116350 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1259389462 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9513274,Human_RBP_ID_10923915,Human_RBP_ID_18571483,Human_RBP_ID_22707965,Human_RBP_ID_23148576 RMVar_hsa_circ_122894,RMVar_hsa_circ_130943 9845 RMVar_ID_9845 Human_SNP_ID_7716179 A-to-I Human chr1 - 29176008 29176008 29176008 GACCTCATGATCCACCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCATGCC GACCTCATGATCCACCTGCCTCGGCCTCCCAACGTGCTGGGATTACAGGTGTGAGCCACCATGCC T G SRSF4 Ensembl:ENSG00000116350 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs944894426 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122894,RMVar_hsa_circ_130943 9846 RMVar_ID_9846 Human_SNP_ID_7716610 A-to-I Human chr1 - 29177410 29177410 29177410 GGGCGTCGTGGCACATGCCTGTAATCCTGGCTACTCGGGAGGCTGAGGCAAGAGAATCACTTGAA GGGCGTCGTGGCACATGCCTGTAATCCTGGCTGCTCGGGAGGCTGAGGCAAGAGAATCACTTGAA T C SRSF4 Ensembl:ENSG00000116350 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs534901456 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11208107 RMVar_hsa_circ_122894,RMVar_hsa_circ_130943 9847 RMVar_ID_9847 Human_SNP_ID_7720778 A-to-I Human chr1 - 29193047 29193047 29193047 CCAGCTACTCGGGAGGTTGAGGTGGGAGGATCACCTGAGCCTGGGAGGTCTAGACTGCAGTGAGC CCAGCTACTCGGGAGGTTGAGGTGGGAGGATCGCCTGAGCCTGGGAGGTCTAGACTGCAGTGAGC T C MECR Ensembl:ENSG00000116353 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1138121 Functional Loss SNV dbSNP153 33..33 33 - - - 9848 RMVar_ID_9848 Human_SNP_ID_7720805 A-to-I Human chr1 - 29193153 29193153 29193153 ATCACTTGAGCCCAGGAGTTCAAGGTCAACCTAGGTAACGTGGTGAAACACCATCTCTACAAAAA ATCACTTGAGCCCAGGAGTTCAAGGTCAACCTGGGTAACGTGGTGAAACACCATCTCTACAAAAA T C MECR Ensembl:ENSG00000116353 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1138115 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8307706 9849 RMVar_ID_9849 Human_SNP_ID_7720811 A-to-I Human chr1 - 29193164 29193164 29193164 AAGGCAAGCGGATCACTTGAGCCCAGGAGTTCAAGGTCAACCTAGGTAACGTGGTGAAACACCAT AAGGCAAGCGGATCACTTGAGCCCAGGAGTTCGAGGTCAACCTAGGTAACGTGGTGAAACACCAT T C MECR Ensembl:ENSG00000116353 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs984201424 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8307706 9850 RMVar_ID_9850 Human_SNP_ID_7720818 A-to-I Human chr1 - 29193195 29193195 29193195 CACACCTGTAATCCCAGCACTTTGGGAAGCCAAGGCAAGCGGATCACTTGAGCCCAGGAGTTCAA CACACCTGTAATCCCAGCACTTTGGGAAGCCAGGGCAAGCGGATCACTTGAGCCCAGGAGTTCAA T C MECR Ensembl:ENSG00000116353 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs896370977 Functional Loss SNV dbSNP153 33..33 33 - - - 9851 RMVar_ID_9851 Human_SNP_ID_7723510 A-to-I Human chr1 - 29204775 29204775 29204775 GTCCTAGTGCAGCAGACACTTTGTTTGCTTGCATCCCATGCCCTAAAGCCACCTCCCATTTAGGC GTCCTAGTGCAGCAGACACTTTGTTTGCTTGCGTCCCATGCCCTAAAGCCACCTCCCATTTAGGC T C MECR Ensembl:ENSG00000116353 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2640463 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_785,GWAS_ID_786,GWAS_ID_787,GWAS_ID_788,GWAS_ID_789,GWAS_ID_790,GWAS_ID_791,GWAS_ID_792,GWAS_ID_793,GWAS_ID_794,GWAS_ID_795,GWAS_ID_796,GWAS_ID_797,GWAS_ID_798,GWAS_ID_799,GWAS_ID_800,GWAS_ID_801,GWAS_ID_802,GWAS_ID_803,GWAS_ID_804,GWAS_ID_805,GWAS_ID_806,GWAS_ID_807,GWAS_ID_808,GWAS_ID_809,GWAS_ID_810,GWAS_ID_811,GWAS_ID_812,GWAS_ID_813,GWAS_ID_814,GWAS_ID_815,GWAS_ID_816,GWAS_ID_817,GWAS_ID_818,GWAS_ID_819,GWAS_ID_820,GWAS_ID_821,GWAS_ID_822,GWAS_ID_823,GWAS_ID_824,GWAS_ID_825,GWAS_ID_826,GWAS_ID_827,GWAS_ID_828,GWAS_ID_829,GWAS_ID_830,GWAS_ID_831,GWAS_ID_832,GWAS_ID_833,GWAS_ID_834,GWAS_ID_835,GWAS_ID_836,GWAS_ID_837,GWAS_ID_838,GWAS_ID_839,GWAS_ID_840,GWAS_ID_841,GWAS_ID_842,GWAS_ID_843,GWAS_ID_844,GWAS_ID_845,GWAS_ID_846,GWAS_ID_847,GWAS_ID_848,GWAS_ID_849,GWAS_ID_850,GWAS_ID_851,GWAS_ID_852,GWAS_ID_853,GWAS_ID_854,GWAS_ID_855,GWAS_ID_856,GWAS_ID_857,GWAS_ID_858,GWAS_ID_859,GWAS_ID_860,GWAS_ID_861,GWAS_ID_862,GWAS_ID_863,GWAS_ID_864,GWAS_ID_865,GWAS_ID_866,GWAS_ID_867,GWAS_ID_868,GWAS_ID_869,GWAS_ID_870,GWAS_ID_871,GWAS_ID_872,GWAS_ID_873,GWAS_ID_874,GWAS_ID_875,GWAS_ID_876,GWAS_ID_877,GWAS_ID_878,GWAS_ID_879,GWAS_ID_880,GWAS_ID_881,GWAS_ID_882,GWAS_ID_883,GWAS_ID_884 RMVar_hsa_circ_26754,RMVar_hsa_circ_353558,RMVar_hsa_circ_79279,RMVar_hsa_circ_6218,RMVar_hsa_circ_130945,RMVar_hsa_circ_130947,RMVar_hsa_circ_370288,RMVar_hsa_circ_55808,RMVar_hsa_circ_130948 9852 RMVar_ID_9852 Human_SNP_ID_396498960 A-to-I Human chr9 + 32413377 32413377 32413377 ATGGTGGTGCATGCCTGTAGTCCCAGCTACTCAGGCGGCTGAGACAGGGGAATCGCTTGAATCTG ATGGTGGTGCATGCCTGTAGTCCCAGCTACTCTGGCGGCTGAGACAGGGGAATCGCTTGAATCTG A T ACO1 Ensembl:ENSG00000122729 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs989849058 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_53536,RMVar_hsa_circ_69919,RMVar_hsa_circ_77085,RMVar_hsa_circ_256284,RMVar_hsa_circ_61358,RMVar_hsa_circ_21927,RMVar_hsa_circ_51803,RMVar_hsa_circ_256286 9853 RMVar_ID_9853 Human_SNP_ID_396509845 A-to-I Human chr9 - 32456370 32456370 32456370 GAGAACATAAAGCCATTTTTATGCTTACTACTAAAAGCTGTCCACTGTAGAGTTGCTGTATGTAG GAGAACATAAAGCCATTTTTATGCTTACTACTGAAAGCTGTCCACTGTAGAGTTGCTGTATGTAG T C DDX58 Ensembl:ENSG00000107201 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1011449534 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2053788 RMVar_hsa_circ_256292,RMVar_hsa_circ_105808,RMVar_hsa_circ_120636,RMVar_hsa_circ_103817,RMVar_hsa_circ_256293,RMVar_hsa_circ_256291 9854 RMVar_ID_9854 Human_SNP_ID_396509866 A-to-I Human chr9 - 32456451 32456451 32456451 CATACAGGTATGTATATGTAATGGTTATATGTACTCATGTTCCTGGTGTAGCAACGTGTGGTATG CATACAGGTATGTATATGTAATGGTTATATGTGCTCATGTTCCTGGTGTAGCAACGTGTGGTATG T C DDX58 Ensembl:ENSG00000107201 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1460248286 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_256292,RMVar_hsa_circ_105808,RMVar_hsa_circ_120636,RMVar_hsa_circ_103817,RMVar_hsa_circ_256293,RMVar_hsa_circ_256291 9855 RMVar_ID_9855 Human_SNP_ID_396534313 A-to-I Human chr9 + 32552446 32552446 32552446 GACTGCTGCCGCCTCCTTACCATGAAGCCAGTAAGTCGTCGCACGCTGGACTGGATTTATTCAGT GACTGCTGCCGCCTCCTTACCATGAAGCCAGTTAGTCGTCGCACGCTGGACTGGATTTATTCAGT A T SMIM27 Ensembl:ENSG00000235453 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1430538048 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_717396 Human_Splice_Rec_1037279,Human_Splice_Rec_1037283,Human_Splice_Rec_1037285,Human_Splice_Rec_1037287 9856 RMVar_ID_9856 Human_SNP_ID_396630134 A-to-I Human chr9 - 32945361 32945361 32945361 GAGGCCTTGCTATGTTGCCCAGGATGGTCTCAAACTCCTGGCCTCAAGAGATCCTCCTGCCTTGG GAGGCCTTGCTATGTTGCCCAGGATGGTCTCAGACTCCTGGCCTCAAGAGATCCTCCTGCCTTGG T C APTX Ensembl:ENSG00000137074 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs532865449 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_256296 9857 RMVar_ID_9857 Human_SNP_ID_396630500 A-to-I Human chr9 - 32946758 32946758 32946758 ATACGGCCCACGCCGTGCTTGCCTGCAACTTCATTCAGGTACACGAAAAGCTCCAAGGAGGTCTG ATACGGCCCACGCCGTGCTTGCCTGCAACTTCGTTCAGGTACACGAAAAGCTCCAAGGAGGTCTG T C APTX Ensembl:ENSG00000137074 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1254577233 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_256297,RMVar_hsa_circ_256296 9858 RMVar_ID_9858 Human_SNP_ID_396631996 A-to-I Human chr9 - 32953149 32953149 32953149 TAGCTCACTGTAACTTCAAACTCCTGGACCCAAGCAATTCTCCCGCCTCAGCCTCCTGAGTAGCT TAGCTCACTGTAACTTCAAACTCCTGGACCCAGGCAATTCTCCCGCCTCAGCCTCCTGAGTAGCT T C APTX Ensembl:ENSG00000137074 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459081839 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_256296 9859 RMVar_ID_9859 Human_SNP_ID_396632009 A-to-I Human chr9 - 32953226 32953226 32953226 AGAAATTCTTTTTCTTTTCTTCCCCTGGAGATAGGGTCTCCCTCTGTCACCCAAGCTGGAGTGCA AGAAATTCTTTTTCTTTTCTTCCCCTGGAGATGGGGTCTCCCTCTGTCACCCAAGCTGGAGTGCA T C APTX Ensembl:ENSG00000137074 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs898349939 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_256296 9860 RMVar_ID_9860 Human_SNP_ID_396632010 A-to-I Human chr9 - 32953226 32953226 32953226 AGAAATTCTTTTTCTTTTCTTCCCCTGGAGATAGGGTCTCCCTCTGTCACCCAAGCTGGAGTGCA AGAAATTCTTTTTCTTTTCTTCCCCTGGAGATCGGGTCTCCCTCTGTCACCCAAGCTGGAGTGCA T G APTX Ensembl:ENSG00000137074 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs898349939 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_256296 9861 RMVar_ID_9861 Human_SNP_ID_396635005 A-to-I Human chr9 - 32965788 32965788 32965788 CAGCCTTCCAAAGTGTTGGGATTATAGGCATAAGCCACTGCACCTGGCCTTTTTGGCCACATTTT CAGCCTTCCAAAGTGTTGGGATTATAGGCATATGCCACTGCACCTGGCCTTTTTGGCCACATTTT T A APTX Ensembl:ENSG00000137074 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355736719 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_256296 9862 RMVar_ID_9862 Human_SNP_ID_396641253 A-to-I Human chr9 - 32990297 32990297 32990297 GTGGTGGCGGGTGCCTGTAATCCCAGCTACTCAGGAGGCTAAGGCAGGAGAATTGCTTGAACCCG GTGGTGGCGGGTGCCTGTAATCCCAGCTACTCGGGAGGCTAAGGCAGGAGAATTGCTTGAACCCG T C APTX Ensembl:ENSG00000137074 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1563973706 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47627,RMVar_hsa_circ_88851,RMVar_hsa_circ_256300 9863 RMVar_ID_9863 Human_SNP_ID_396643599 A-to-I Human chr9 - 32999854 32999854 32999854 CCGGGTTCACGCCATTCTCCTGGCTCAGGACTACAGGCGTCTACCACCACGCCCGGCTAATTTTT CCGGGTTCACGCCATTCTCCTGGCTCAGGACTGCAGGCGTCTACCACCACGCCCGGCTAATTTTT T C APTX Ensembl:ENSG00000137074 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1231988032 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16653651 9864 RMVar_ID_9864 Human_SNP_ID_396644990 A-to-I Human chr9 - 33004091 33004091 33004091 TTGCTTCAAAAGACATTATTTCATTCTTCTTTATGGCTGAGTAGTATTCTGTGGTGTATATGTAC TTGCTTCAAAAGACATTATTTCATTCTTCTTTTTGGCTGAGTAGTATTCTGTGGTGTATATGTAC T A APTX Ensembl:ENSG00000137074 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs996192261 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16653837,Human_RBP_ID_18134882 9865 RMVar_ID_9865 Human_SNP_ID_396645588 A-to-I Human chr9 - 33006238 33006238 33006238 TAAAATTTTTTTTATAGAGAGAGGGTCTTGCTATGTTGGCTGGGCTGATCTTGAACTCCTGGCCT TAAAATTTTTTTTATAGAGAGAGGGTCTTGCTGTGTTGGCTGGGCTGATCTTGAACTCCTGGCCT T C APTX Ensembl:ENSG00000137074 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs927075356 Functional Loss SNV dbSNP153 33..33 33 - - - 9866 RMVar_ID_9866 Human_SNP_ID_396646925 A-to-I Human chr9 - 33011129 33011129 33011129 TTTTTTTTTTCTTTTTTTTGAGACGGAGTCTCACTCTGTCACGCAGGCTGTAGTGCAGTGGCACG TTTTTTTTTTCTTTTTTTTGAGACGGAGTCTCGCTCTGTCACGCAGGCTGTAGTGCAGTGGCACG T C APTX Ensembl:ENSG00000137074 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1187970286 Functional Loss SNV dbSNP153 33..33 33 - - - 9867 RMVar_ID_9867 Human_SNP_ID_396652214 A-to-I Human chr9 + 33027607 33027607 33027607 CCGCGTGCTGTGGCTCATTCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGTGGATCACTGAG CCGCGTGCTGTGGCTCATTCTGTAATCCCAGCCCTTTGGGAGGCCGAGGTGGGTGGATCACTGAG A C DNAJA1 Ensembl:ENSG00000086061 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1057419544 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26219387 RMVar_hsa_circ_86836,RMVar_hsa_circ_256303,RMVar_hsa_circ_96396,RMVar_hsa_circ_349821,RMVar_hsa_circ_256301,RMVar_hsa_circ_370293,RMVar_hsa_circ_5531,RMVar_hsa_circ_54199,RMVar_hsa_circ_256304,RMVar_hsa_circ_107549,RMVar_hsa_circ_301590,RMVar_hsa_circ_268605,RMVar_hsa_circ_256305 9868 RMVar_ID_9868 Human_SNP_ID_396652256 A-to-I Human chr9 + 33027723 33027723 33027723 AACTACAGAATTAGCTGGGCGTGGTGGTGGGCATCTGCAATCCCAGCTCCTCTGGAGGCTGAGGC AACTACAGAATTAGCTGGGCGTGGTGGTGGGCGTCTGCAATCCCAGCTCCTCTGGAGGCTGAGGC A G DNAJA1 Ensembl:ENSG00000086061 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs12351356 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86836,RMVar_hsa_circ_256303,RMVar_hsa_circ_96396,RMVar_hsa_circ_349821,RMVar_hsa_circ_256301,RMVar_hsa_circ_370293,RMVar_hsa_circ_5531,RMVar_hsa_circ_54199,RMVar_hsa_circ_256304,RMVar_hsa_circ_107549,RMVar_hsa_circ_301590,RMVar_hsa_circ_268605,RMVar_hsa_circ_256305 9869 RMVar_ID_9869 Human_SNP_ID_396654494 A-to-I Human chr9 + 33034991 33034991 33034991 GAAGAGTGGCTTGAACTCAGGAGTTCAAGGTTATGATCATGCCACTGCATTCTAGCCTGGGTGAC GAAGAGTGGCTTGAACTCAGGAGTTCAAGGTTGTGATCATGCCACTGCATTCTAGCCTGGGTGAC A G DNAJA1 Ensembl:ENSG00000086061 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs574091665 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86836,RMVar_hsa_circ_256303,RMVar_hsa_circ_96396,RMVar_hsa_circ_256301,RMVar_hsa_circ_370293,RMVar_hsa_circ_256304,RMVar_hsa_circ_107549,RMVar_hsa_circ_268605,RMVar_hsa_circ_256305,RMVar_hsa_circ_14217,RMVar_hsa_circ_57567,RMVar_hsa_circ_256308,RMVar_hsa_circ_76021,RMVar_hsa_circ_278707,RMVar_hsa_circ_256307 9870 RMVar_ID_9870 Human_SNP_ID_396654600 A-to-I Human chr9 + 33035234 33035234 33035234 CATGGTGAAATGCCATCTCTGTTAAAAATTAAAAAATTAGCCAGGCATGGTGGCAGGCCCTGAGG CATGGTGAAATGCCATCTCTGTTAAAAATTAAGAAATTAGCCAGGCATGGTGGCAGGCCCTGAGG A G DNAJA1 Ensembl:ENSG00000086061 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs773786250 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23316663,Human_RBP_ID_26219428 RMVar_hsa_circ_86836,RMVar_hsa_circ_256303,RMVar_hsa_circ_96396,RMVar_hsa_circ_256301,RMVar_hsa_circ_370293,RMVar_hsa_circ_256304,RMVar_hsa_circ_107549,RMVar_hsa_circ_268605,RMVar_hsa_circ_256305,RMVar_hsa_circ_14217,RMVar_hsa_circ_57567,RMVar_hsa_circ_256308,RMVar_hsa_circ_76021,RMVar_hsa_circ_278707,RMVar_hsa_circ_256307 9871 RMVar_ID_9871 Human_SNP_ID_396654773 A-to-I Human chr9 + 33035669 33035669 33035669 TTTTTGTATTTTTAGTAGAGACGGGTTTCACCATGTTGGCCAGGCTGGTATCGAACTCCTGACCT TTTTTGTATTTTTAGTAGAGACGGGTTTCACCGTGTTGGCCAGGCTGGTATCGAACTCCTGACCT A G DNAJA1 Ensembl:ENSG00000086061 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs965609620 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86836,RMVar_hsa_circ_256303,RMVar_hsa_circ_96396,RMVar_hsa_circ_256301,RMVar_hsa_circ_370293,RMVar_hsa_circ_256304,RMVar_hsa_circ_107549,RMVar_hsa_circ_268605,RMVar_hsa_circ_256305,RMVar_hsa_circ_14217,RMVar_hsa_circ_57567,RMVar_hsa_circ_256308,RMVar_hsa_circ_76021,RMVar_hsa_circ_278707,RMVar_hsa_circ_256307 9872 RMVar_ID_9872 Human_SNP_ID_396654914 A-to-I Human chr9 + 33036144 33036144 33036144 TTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTTCAGACCT TTTTGTATTTTTAGTAGAGATGGGGTTTCACCGTGTTGGCCAGGCTGGTCTTGAACTTCAGACCT A G DNAJA1 Ensembl:ENSG00000086061 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs867936900 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1037946 RMVar_hsa_circ_86836,RMVar_hsa_circ_256303,RMVar_hsa_circ_96396,RMVar_hsa_circ_256301,RMVar_hsa_circ_370293,RMVar_hsa_circ_256304,RMVar_hsa_circ_107549,RMVar_hsa_circ_268605,RMVar_hsa_circ_256305,RMVar_hsa_circ_14217,RMVar_hsa_circ_57567,RMVar_hsa_circ_256308,RMVar_hsa_circ_76021,RMVar_hsa_circ_278707,RMVar_hsa_circ_256307 9873 RMVar_ID_9873 Human_SNP_ID_396655571 A-to-I Human chr9 + 33038084 33038084 33038084 TGGAGTGCAGTGGTGCGATCCTGGATCACTGTAACCTCCACCTCCTGGGTTCAAGCAGTTCTCCT TGGAGTGCAGTGGTGCGATCCTGGATCACTGTTACCTCCACCTCCTGGGTTCAAGCAGTTCTCCT A T DNAJA1 Ensembl:ENSG00000086061 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs187142025 Functional Loss SNV dbSNP153 33..33 33 - - - 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_256310 9874 RMVar_ID_9874 Human_SNP_ID_396655578 A-to-I Human chr9 + 33038108 33038108 33038108 ATCACTGTAACCTCCACCTCCTGGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCTGAGTAGCTGGG ATCACTGTAACCTCCACCTCCTGGGTTCAAGCGGTTCTCCTGCCTCAGCCTCCTGAGTAGCTGGG A G DNAJA1 Ensembl:ENSG00000086061 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1326689148 Functional Loss SNV dbSNP153 33..33 33 - - - 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_256310 9875 RMVar_ID_9875 Human_SNP_ID_396655584 A-to-I Human chr9 + 33038134 33038134 33038134 TCAAGCAGTTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGAATACAGGTGCCCGCCACCACGCTGG TCAAGCAGTTCTCCTGCCTCAGCCTCCTGAGTGGCTGGGAATACAGGTGCCCGCCACCACGCTGG A G DNAJA1 Ensembl:ENSG00000086061 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs529220295 Functional Loss SNV dbSNP153 33..33 33 - - - 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_256310 9876 RMVar_ID_9876 Human_SNP_ID_396657169 A-to-I Human chr9 - 33043114 33043107 33043114 TAAAACTTACAATAGGCCGGGCACGGTGGCTCAAGCCTGTAATCCCAGCACTTTGGGAGGCCGAG TAAAACTTACAATAGGCCGGGCACGGTGGCTC_______TAATCCCAGCACTTTGGGAGGCCGAG ACAGGCTT A SMU1 Ensembl:ENSG00000122692 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1209751562 Functional Loss DEL dbSNP153 33..39 33 - - - RMVar_hsa_circ_83277,RMVar_hsa_circ_126359,RMVar_hsa_circ_97689,RMVar_hsa_circ_256312,RMVar_hsa_circ_256314,RMVar_hsa_circ_80712,RMVar_hsa_circ_256315,RMVar_hsa_circ_256313 9877 RMVar_ID_9877 Human_SNP_ID_396657361 A-to-I Human chr9 - 33043914 33043914 33043914 CCAGTTGTTTTTTTTCAGCATGTATTATTACTACCACTAACGGCCTCTGTTGAGCCCTTCCTTGC CCAGTTGTTTTTTTTCAGCATGTATTATTACTTCCACTAACGGCCTCTGTTGAGCCCTTCCTTGC T A SMU1 Ensembl:ENSG00000122692 Protein coding 3'UTR GSE47997;GSE100210;GSE107867 K562 cells&HepG2 cells;HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 23474544,29129909,30559470 RNA-Seq:(High) rs949429664 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3210595 RMVar_hsa_circ_83277,RMVar_hsa_circ_126359,RMVar_hsa_circ_97689,RMVar_hsa_circ_256312,RMVar_hsa_circ_256314,RMVar_hsa_circ_80712,RMVar_hsa_circ_256315,RMVar_hsa_circ_256313 9878 RMVar_ID_9878 Human_SNP_ID_396664969 A-to-I Human chr9 - 33074566 33074566 33074566 TTGCTCTCTTTCCCAGGCTAGAGTGCAGTGGCATGATCACGGCTCACTGCAGCCTCAACCTTATG TTGCTCTCTTTCCCAGGCTAGAGTGCAGTGGCGTGATCACGGCTCACTGCAGCCTCAACCTTATG T C SMU1 Ensembl:ENSG00000122692 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs947306397 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97689,RMVar_hsa_circ_256315 9879 RMVar_ID_9879 Human_SNP_ID_396675109 A-to-I Human chr9 - 33113139 33113139 33113139 ATTTGGTGGCCGTGGAACACATTCCCGGTGATAGAATTGCTAAATTGTCGTGAAATAGGTTAGAA ATTTGGTGGCCGTGGAACACATTCCCGGTGATGGAATTGCTAAATTGTCGTGAAATAGGTTAGAA T C B4GALT1 Ensembl:ENSG00000086062 Protein coding intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1049105472 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_717699,Human_RBP_ID_21659565,Human_RBP_ID_24299417,Human_RBP_ID_26566753 Human_miRNA_ID_2698799 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 9880 RMVar_ID_9880 Human_SNP_ID_396676118 A-to-I Human chr9 - 33116625 33116625 33116625 CCAGCTACTTGGGAGGCTGAGACAGGAGAATTACTTGAAAACCTGGGAGGCGGAGGTTGCAGTGA CCAGCTACTTGGGAGGCTGAGACAGGAGAATTTCTTGAAAACCTGGGAGGCGGAGGTTGCAGTGA T A B4GALT1 Ensembl:ENSG00000086062 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1007846780 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113644,RMVar_hsa_circ_97414,RMVar_hsa_circ_91506,RMVar_hsa_circ_256330,RMVar_hsa_circ_256331,RMVar_hsa_circ_256332,RMVar_hsa_circ_256333,RMVar_hsa_circ_319028 9881 RMVar_ID_9881 Human_SNP_ID_396676381 A-to-I Human chr9 - 33117775 33117775 33117775 GTAGTATGAGGTGTGCCAAAGGTGGATGACTCAGCACCTAAGTGATGACACCTAATTACGAATAG GTAGTATGAGGTGTGCCAAAGGTGGATGACTCTGCACCTAAGTGATGACACCTAATTACGAATAG T A B4GALT1 Ensembl:ENSG00000086062 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7851385 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_885 RMVar_hsa_circ_113644,RMVar_hsa_circ_97414,RMVar_hsa_circ_91506,RMVar_hsa_circ_256330,RMVar_hsa_circ_256331,RMVar_hsa_circ_256332,RMVar_hsa_circ_256333,RMVar_hsa_circ_319028 9882 RMVar_ID_9882 Human_SNP_ID_396676382 A-to-I Human chr9 - 33117775 33117775 33117775 GTAGTATGAGGTGTGCCAAAGGTGGATGACTCAGCACCTAAGTGATGACACCTAATTACGAATAG GTAGTATGAGGTGTGCCAAAGGTGGATGACTCGGCACCTAAGTGATGACACCTAATTACGAATAG T C B4GALT1 Ensembl:ENSG00000086062 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7851385 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_885 RMVar_hsa_circ_113644,RMVar_hsa_circ_97414,RMVar_hsa_circ_91506,RMVar_hsa_circ_256330,RMVar_hsa_circ_256331,RMVar_hsa_circ_256332,RMVar_hsa_circ_256333,RMVar_hsa_circ_319028 9883 RMVar_ID_9883 Human_SNP_ID_396676863 A-to-I Human chr9 - 33119572 33119572 33119572 AGTTGGGACTACAGGCATGAGCCAGCATGTCCAGCTAATTTTTTATTTTTAGTGGAGATGAGGTC AGTTGGGACTACAGGCATGAGCCAGCATGTCCGGCTAATTTTTTATTTTTAGTGGAGATGAGGTC T C B4GALT1 Ensembl:ENSG00000086062 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1300208014 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113644,RMVar_hsa_circ_97414,RMVar_hsa_circ_91506,RMVar_hsa_circ_256330,RMVar_hsa_circ_256331,RMVar_hsa_circ_256332,RMVar_hsa_circ_256333,RMVar_hsa_circ_319028 9884 RMVar_ID_9884 Human_SNP_ID_396676880 A-to-I Human chr9 - 33119669 33119669 33119669 CTCTGTCACCCAGGCTGGAGTGCAGTGACACAATCATGGCTCACTGCAGCCTTGACTGCCTGGGC CTCTGTCACCCAGGCTGGAGTGCAGTGACACAGTCATGGCTCACTGCAGCCTTGACTGCCTGGGC T C B4GALT1 Ensembl:ENSG00000086062 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs936990946 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113644,RMVar_hsa_circ_97414,RMVar_hsa_circ_91506,RMVar_hsa_circ_256330,RMVar_hsa_circ_256331,RMVar_hsa_circ_256332,RMVar_hsa_circ_256333,RMVar_hsa_circ_319028 9885 RMVar_ID_9885 Human_SNP_ID_396676950 A-to-I Human chr9 - 33119966 33119966 33119966 TTGCCCAGTCTGGTCTCGAACTCCTGAGCTCAAGCAATCCATCTGCCTTGGCCTCTCGAAGTGCT TTGCCCAGTCTGGTCTCGAACTCCTGAGCTCAGGCAATCCATCTGCCTTGGCCTCTCGAAGTGCT T C B4GALT1 Ensembl:ENSG00000086062 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs958452063 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113644,RMVar_hsa_circ_97414,RMVar_hsa_circ_91506,RMVar_hsa_circ_256330,RMVar_hsa_circ_256331,RMVar_hsa_circ_256332,RMVar_hsa_circ_256333,RMVar_hsa_circ_319028 9886 RMVar_ID_9886 Human_SNP_ID_396676965 A-to-I Human chr9 - 33120049 33120040 33120050 CTCCTGAGTAGCTGGGACTACAAACACTTGCCACCATGCGCAGCTAATTTTTGTATATTTTGTAG CTCCTGAGTAGCTGGGACTACAAACACTTGC__________AGCTAATTTTTGTATATTTTGTAG TGCGCATGGTG T B4GALT1 Ensembl:ENSG00000086062 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1268371571 Functional Loss DEL dbSNP153 32..41 33 - - - RMVar_hsa_circ_113644,RMVar_hsa_circ_97414,RMVar_hsa_circ_91506,RMVar_hsa_circ_256330,RMVar_hsa_circ_256331,RMVar_hsa_circ_256332,RMVar_hsa_circ_256333,RMVar_hsa_circ_319028 9887 RMVar_ID_9887 Human_SNP_ID_396676970 A-to-I Human chr9 - 33120056 33120056 33120056 CCTCAGCCTCCTGAGTAGCTGGGACTACAAACACTTGCCACCATGCGCAGCTAATTTTTGTATAT CCTCAGCCTCCTGAGTAGCTGGGACTACAAACGCTTGCCACCATGCGCAGCTAATTTTTGTATAT T C B4GALT1 Ensembl:ENSG00000086062 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs748208148 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113644,RMVar_hsa_circ_97414,RMVar_hsa_circ_91506,RMVar_hsa_circ_256330,RMVar_hsa_circ_256331,RMVar_hsa_circ_256332,RMVar_hsa_circ_256333,RMVar_hsa_circ_319028 9888 RMVar_ID_9888 Human_SNP_ID_396676971 A-to-I Human chr9 - 33120062 33120062 33120062 CTGTCACCTCAGCCTCCTGAGTAGCTGGGACTACAAACACTTGCCACCATGCGCAGCTAATTTTT CTGTCACCTCAGCCTCCTGAGTAGCTGGGACTGCAAACACTTGCCACCATGCGCAGCTAATTTTT T C B4GALT1 Ensembl:ENSG00000086062 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1210681473 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113644,RMVar_hsa_circ_97414,RMVar_hsa_circ_91506,RMVar_hsa_circ_256330,RMVar_hsa_circ_256331,RMVar_hsa_circ_256332,RMVar_hsa_circ_256333,RMVar_hsa_circ_319028 9889 RMVar_ID_9889 Human_SNP_ID_396676974 A-to-I Human chr9 - 33120072 33120072 33120072 TCATGCCATCCTGTCACCTCAGCCTCCTGAGTAGCTGGGACTACAAACACTTGCCACCATGCGCA TCATGCCATCCTGTCACCTCAGCCTCCTGAGTGGCTGGGACTACAAACACTTGCCACCATGCGCA T C B4GALT1 Ensembl:ENSG00000086062 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs942183227 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113644,RMVar_hsa_circ_97414,RMVar_hsa_circ_91506,RMVar_hsa_circ_256330,RMVar_hsa_circ_256331,RMVar_hsa_circ_256332,RMVar_hsa_circ_256333,RMVar_hsa_circ_319028 9890 RMVar_ID_9890 Human_SNP_ID_396682796 A-to-I Human chr9 - 33143062 33143061 33143062 CGGCTCACTGCAGCCTCCACTTCCCAGGTTCCAGCGATTCTCCTGCCTCAGCCTCCCAGGTAGCT CGGCTCACTGCAGCCTCCACTTCCCAGGTTCC_GCGATTCTCCTGCCTCAGCCTCCCAGGTAGCT CT C B4GALT1 Ensembl:ENSG00000086062 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1162187751 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_97414,RMVar_hsa_circ_256332 9891 RMVar_ID_9891 Human_SNP_ID_396710318 A-to-I Human chr9 - 33251532 33251532 33251532 GTTGGCCAGGCTGGTCTCGAACTCCTGAGCTTAAGCAATCTGTCTGTCTTGGCCTCCCAAAGTGA GTTGGCCAGGCTGGTCTCGAACTCCTGAGCTTGAGCAATCTGTCTGTCTTGGCCTCCCAAAGTGA T C BAG1 Ensembl:ENSG00000107262 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs552483476 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26219609 9892 RMVar_ID_9892 Human_SNP_ID_396715820 A-to-I Human chr9 + 33272996 33272995 33272997 TGCTTGTCTTTTTTTGTTGTTGTTGTTGAGACAGAGTCTCGTTCTGTCACCAAGGCTGGAGTGCA TGCTTGTCTTTTTTTGTTGTTGTTGTTGAGAC__AGTCTCGTTCTGTCACCAAGGCTGGAGTGCA CAG C CHMP5 Ensembl:ENSG00000086065 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs778299871 Functional Loss DEL dbSNP153 33..34 33 - - - 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_373405,RMVar_hsa_circ_256338 9893 RMVar_ID_9893 Human_SNP_ID_396721431 A-to-I Human chr9 + 33296141 33296141 33296141 TAGAAATGGGGTTTCACCATGTTGGCCAGGCTAGTCTCAAACTTCTGACCTCGGGTGATCCGCCT TAGAAATGGGGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTTCTGACCTCGGGTGATCCGCCT A G NFX1 Ensembl:ENSG00000086102 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs954588099 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_330809,RMVar_hsa_circ_256340,RMVar_hsa_circ_115958,RMVar_hsa_circ_363498,RMVar_hsa_circ_60474,RMVar_hsa_circ_256344 9894 RMVar_ID_9894 Human_SNP_ID_396724301 A-to-I Human chr9 + 33308073 33308073 33308073 GCAATCTGCTCTCCTCAGCCTCCCAACATGCCAGGATTACTGGTGTGAGCCACCACACCCAGCCA GCAATCTGCTCTCCTCAGCCTCCCAACATGCCGGGATTACTGGTGTGAGCCACCACACCCAGCCA A G NFX1 Ensembl:ENSG00000086102 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1199744092 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2173,RMVar_hsa_circ_32295,RMVar_hsa_circ_256340,RMVar_hsa_circ_115958,RMVar_hsa_circ_363498,RMVar_hsa_circ_60474,RMVar_hsa_circ_124237,RMVar_hsa_circ_32127,RMVar_hsa_circ_126375,RMVar_hsa_circ_256345,RMVar_hsa_circ_72559,RMVar_hsa_circ_89095,RMVar_hsa_circ_256346,RMVar_hsa_circ_256347 9895 RMVar_ID_9895 Human_SNP_ID_396724356 A-to-I Human chr9 + 33308315 33308315 33308315 AAATTTAAAATTAGCCAGCTGTGGTGGCACACACCTGTAGTCCCAGCTACTTGGGAGGCTGAGCA AAATTTAAAATTAGCCAGCTGTGGTGGCACACGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGCA A G NFX1 Ensembl:ENSG00000086102 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs191943190 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2173,RMVar_hsa_circ_32295,RMVar_hsa_circ_256340,RMVar_hsa_circ_115958,RMVar_hsa_circ_363498,RMVar_hsa_circ_60474,RMVar_hsa_circ_124237,RMVar_hsa_circ_32127,RMVar_hsa_circ_126375,RMVar_hsa_circ_256345,RMVar_hsa_circ_72559,RMVar_hsa_circ_89095,RMVar_hsa_circ_256346,RMVar_hsa_circ_256347 9896 RMVar_ID_9896 Human_SNP_ID_396724360 A-to-I Human chr9 + 33308331 33308331 33308331 AGCTGTGGTGGCACACACCTGTAGTCCCAGCTACTTGGGAGGCTGAGCAAGGAGGATCATTTGAG AGCTGTGGTGGCACACACCTGTAGTCCCAGCTGCTTGGGAGGCTGAGCAAGGAGGATCATTTGAG A G NFX1 Ensembl:ENSG00000086102 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs534799507 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16656731 RMVar_hsa_circ_2173,RMVar_hsa_circ_32295,RMVar_hsa_circ_256340,RMVar_hsa_circ_115958,RMVar_hsa_circ_363498,RMVar_hsa_circ_60474,RMVar_hsa_circ_124237,RMVar_hsa_circ_32127,RMVar_hsa_circ_126375,RMVar_hsa_circ_256345,RMVar_hsa_circ_72559,RMVar_hsa_circ_89095,RMVar_hsa_circ_256346,RMVar_hsa_circ_256347 9897 RMVar_ID_9897 Human_SNP_ID_396724703 A-to-I Human chr9 + 33309651 33309650 33309652 TACACTTGTTAGGACTCAAAAGTGACAGAGACAGGGTCTCGCTCTGTTGCCCAGGCTTGAGTGCA TACACTTGTTAGGACTCAAAAGTGACAGAGAC__GGTCTCGCTCTGTTGCCCAGGCTTGAGTGCA CAG C NFX1 Ensembl:ENSG00000086102 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1020167689 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_3899032,Human_RBP_ID_16656758 RMVar_hsa_circ_2173,RMVar_hsa_circ_32295,RMVar_hsa_circ_256340,RMVar_hsa_circ_115958,RMVar_hsa_circ_363498,RMVar_hsa_circ_60474,RMVar_hsa_circ_124237,RMVar_hsa_circ_32127,RMVar_hsa_circ_126375,RMVar_hsa_circ_256345,RMVar_hsa_circ_72559,RMVar_hsa_circ_89095,RMVar_hsa_circ_256346,RMVar_hsa_circ_256347 9898 RMVar_ID_9898 Human_SNP_ID_396724704 A-to-I Human chr9 + 33309651 33309651 33309651 TACACTTGTTAGGACTCAAAAGTGACAGAGACAGGGTCTCGCTCTGTTGCCCAGGCTTGAGTGCA TACACTTGTTAGGACTCAAAAGTGACAGAGACGGGGTCTCGCTCTGTTGCCCAGGCTTGAGTGCA A G NFX1 Ensembl:ENSG00000086102 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404276930 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3899032,Human_RBP_ID_16656758 RMVar_hsa_circ_2173,RMVar_hsa_circ_32295,RMVar_hsa_circ_256340,RMVar_hsa_circ_115958,RMVar_hsa_circ_363498,RMVar_hsa_circ_60474,RMVar_hsa_circ_124237,RMVar_hsa_circ_32127,RMVar_hsa_circ_126375,RMVar_hsa_circ_256345,RMVar_hsa_circ_72559,RMVar_hsa_circ_89095,RMVar_hsa_circ_256346,RMVar_hsa_circ_256347 9899 RMVar_ID_9899 Human_SNP_ID_396725764 A-to-I Human chr9 + 33314183 33314183 33314183 TTTTTGTGTTTTTAGTAGAGATAGGGTTTCACAATGTTGGCCAGGCTGGTCTTGAACTCCTGACC TTTTTGTGTTTTTAGTAGAGATAGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGACC A C NFX1 Ensembl:ENSG00000086102 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs765442784 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2173,RMVar_hsa_circ_32295,RMVar_hsa_circ_256340,RMVar_hsa_circ_115958,RMVar_hsa_circ_363498,RMVar_hsa_circ_124237,RMVar_hsa_circ_32127,RMVar_hsa_circ_126375,RMVar_hsa_circ_256345,RMVar_hsa_circ_89095,RMVar_hsa_circ_256346,RMVar_hsa_circ_31540,RMVar_hsa_circ_270281,RMVar_hsa_circ_317000,RMVar_hsa_circ_343439,RMVar_hsa_circ_256347,RMVar_hsa_circ_359171,RMVar_hsa_circ_321093,RMVar_hsa_circ_65108,RMVar_hsa_circ_87501,RMVar_hsa_circ_55967,RMVar_hsa_circ_256350,RMVar_hsa_circ_256351,RMVar_hsa_circ_256349,RMVar_hsa_circ_304142 9900 RMVar_ID_9900 Human_SNP_ID_396726480 A-to-I Human chr9 + 33317177 33317177 33317177 GTAGTGGCTCACACCTGTAATCCCAGCACTTTAGGAGGCCAGGATGGGCTGATCACTTGAGCCCA GTAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAGGATGGGCTGATCACTTGAGCCCA A G NFX1 Ensembl:ENSG00000086102 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs706129 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16656965 GWAS_ID_886,GWAS_ID_887,GWAS_ID_888,GWAS_ID_889,GWAS_ID_890,GWAS_ID_891,GWAS_ID_892,GWAS_ID_893,GWAS_ID_894,GWAS_ID_895,GWAS_ID_896,GWAS_ID_897,GWAS_ID_898,GWAS_ID_899,GWAS_ID_900,GWAS_ID_901,GWAS_ID_902,GWAS_ID_903,GWAS_ID_904,GWAS_ID_905,GWAS_ID_906,GWAS_ID_907,GWAS_ID_908,GWAS_ID_909,GWAS_ID_910,GWAS_ID_911,GWAS_ID_912,GWAS_ID_913,GWAS_ID_914,GWAS_ID_915,GWAS_ID_916,GWAS_ID_917,GWAS_ID_918,GWAS_ID_919,GWAS_ID_920,GWAS_ID_921,GWAS_ID_922,GWAS_ID_923,GWAS_ID_924,GWAS_ID_925,GWAS_ID_926,GWAS_ID_927,GWAS_ID_928,GWAS_ID_929,GWAS_ID_930,GWAS_ID_931,GWAS_ID_932,GWAS_ID_933,GWAS_ID_934,GWAS_ID_935,GWAS_ID_936,GWAS_ID_937,GWAS_ID_938,GWAS_ID_939,GWAS_ID_940,GWAS_ID_941,GWAS_ID_942,GWAS_ID_943,GWAS_ID_944,GWAS_ID_945,GWAS_ID_946,GWAS_ID_947,GWAS_ID_948,GWAS_ID_949,GWAS_ID_950,GWAS_ID_951,GWAS_ID_952,GWAS_ID_953,GWAS_ID_954,GWAS_ID_955,GWAS_ID_956,GWAS_ID_957,GWAS_ID_958,GWAS_ID_959,GWAS_ID_960,GWAS_ID_961,GWAS_ID_962,GWAS_ID_963,GWAS_ID_964,GWAS_ID_965,GWAS_ID_966,GWAS_ID_967,GWAS_ID_968,GWAS_ID_969,GWAS_ID_970 RMVar_hsa_circ_2173,RMVar_hsa_circ_32295,RMVar_hsa_circ_256340,RMVar_hsa_circ_115958,RMVar_hsa_circ_363498,RMVar_hsa_circ_124237,RMVar_hsa_circ_32127,RMVar_hsa_circ_126375,RMVar_hsa_circ_256345,RMVar_hsa_circ_89095,RMVar_hsa_circ_256346,RMVar_hsa_circ_31540,RMVar_hsa_circ_270281,RMVar_hsa_circ_317000,RMVar_hsa_circ_343439,RMVar_hsa_circ_256347,RMVar_hsa_circ_359171,RMVar_hsa_circ_321093,RMVar_hsa_circ_65108,RMVar_hsa_circ_87501,RMVar_hsa_circ_55967,RMVar_hsa_circ_256350,RMVar_hsa_circ_256351,RMVar_hsa_circ_256349,RMVar_hsa_circ_304142 9901 RMVar_ID_9901 Human_SNP_ID_396726481 A-to-I Human chr9 + 33317177 33317177 33317177 GTAGTGGCTCACACCTGTAATCCCAGCACTTTAGGAGGCCAGGATGGGCTGATCACTTGAGCCCA GTAGTGGCTCACACCTGTAATCCCAGCACTTTTGGAGGCCAGGATGGGCTGATCACTTGAGCCCA A T NFX1 Ensembl:ENSG00000086102 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs706129 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16656965 GWAS_ID_886,GWAS_ID_887,GWAS_ID_888,GWAS_ID_889,GWAS_ID_890,GWAS_ID_891,GWAS_ID_892,GWAS_ID_893,GWAS_ID_894,GWAS_ID_895,GWAS_ID_896,GWAS_ID_897,GWAS_ID_898,GWAS_ID_899,GWAS_ID_900,GWAS_ID_901,GWAS_ID_902,GWAS_ID_903,GWAS_ID_904,GWAS_ID_905,GWAS_ID_906,GWAS_ID_907,GWAS_ID_908,GWAS_ID_909,GWAS_ID_910,GWAS_ID_911,GWAS_ID_912,GWAS_ID_913,GWAS_ID_914,GWAS_ID_915,GWAS_ID_916,GWAS_ID_917,GWAS_ID_918,GWAS_ID_919,GWAS_ID_920,GWAS_ID_921,GWAS_ID_922,GWAS_ID_923,GWAS_ID_924,GWAS_ID_925,GWAS_ID_926,GWAS_ID_927,GWAS_ID_928,GWAS_ID_929,GWAS_ID_930,GWAS_ID_931,GWAS_ID_932,GWAS_ID_933,GWAS_ID_934,GWAS_ID_935,GWAS_ID_936,GWAS_ID_937,GWAS_ID_938,GWAS_ID_939,GWAS_ID_940,GWAS_ID_941,GWAS_ID_942,GWAS_ID_943,GWAS_ID_944,GWAS_ID_945,GWAS_ID_946,GWAS_ID_947,GWAS_ID_948,GWAS_ID_949,GWAS_ID_950,GWAS_ID_951,GWAS_ID_952,GWAS_ID_953,GWAS_ID_954,GWAS_ID_955,GWAS_ID_956,GWAS_ID_957,GWAS_ID_958,GWAS_ID_959,GWAS_ID_960,GWAS_ID_961,GWAS_ID_962,GWAS_ID_963,GWAS_ID_964,GWAS_ID_965,GWAS_ID_966,GWAS_ID_967,GWAS_ID_968,GWAS_ID_969,GWAS_ID_970 RMVar_hsa_circ_2173,RMVar_hsa_circ_32295,RMVar_hsa_circ_256340,RMVar_hsa_circ_115958,RMVar_hsa_circ_363498,RMVar_hsa_circ_124237,RMVar_hsa_circ_32127,RMVar_hsa_circ_126375,RMVar_hsa_circ_256345,RMVar_hsa_circ_89095,RMVar_hsa_circ_256346,RMVar_hsa_circ_31540,RMVar_hsa_circ_270281,RMVar_hsa_circ_317000,RMVar_hsa_circ_343439,RMVar_hsa_circ_256347,RMVar_hsa_circ_359171,RMVar_hsa_circ_321093,RMVar_hsa_circ_65108,RMVar_hsa_circ_87501,RMVar_hsa_circ_55967,RMVar_hsa_circ_256350,RMVar_hsa_circ_256351,RMVar_hsa_circ_256349,RMVar_hsa_circ_304142 9902 RMVar_ID_9902 Human_SNP_ID_396736718 A-to-I Human chr9 + 33357582 33357582 33357582 GAGATAGGATCTTGCTCTGTCACCCATGCTGGAATGTAGTGGCACAATCATAGTTCACTGTACCC GAGATAGGATCTTGCTCTGTCACCCATGCTGGGATGTAGTGGCACAATCATAGTTCACTGTACCC A G NFX1 Ensembl:ENSG00000086102 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1032822916 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59542,RMVar_hsa_circ_95828,RMVar_hsa_circ_368021,RMVar_hsa_circ_256368,RMVar_hsa_circ_78948,RMVar_hsa_circ_256369,RMVar_hsa_circ_256367 9903 RMVar_ID_9903 Human_SNP_ID_396736740 A-to-I Human chr9 + 33357671 33357671 33357671 CTCGTGCCTCAGCCTCCAAAATAGATAGGACTACAGGCACACACCACTACGCCTGGCTAAGATTT CTCGTGCCTCAGCCTCCAAAATAGATAGGACTGCAGGCACACACCACTACGCCTGGCTAAGATTT A G NFX1 Ensembl:ENSG00000086102 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs962276656 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59542,RMVar_hsa_circ_95828,RMVar_hsa_circ_368021,RMVar_hsa_circ_256368,RMVar_hsa_circ_78948,RMVar_hsa_circ_256369,RMVar_hsa_circ_256367 9904 RMVar_ID_9904 Human_SNP_ID_396764563 A-to-I Human chr9 - 33456512 33456512 33456512 GAACCCTGATGTAAGGCTGGGCGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGCA GAACCCTGATGTAAGGCTGGGCGCAGTGGCTCTCACCTGTAATCCCAGCACTTTGGGAGGCCGCA T A RF00017-4575,lnc-BAG1-2 RNACentral:URS0000918622,RNACentral:URS00008C194B SRP RNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978193193 Functional Loss SNV dbSNP153 33..33 33 - - - 9905 RMVar_ID_9905 Human_SNP_ID_396769523 A-to-I Human chr9 - 33472781 33472781 33472781 TTTAATAGAGACGGAGTTTCCCCATGTTGGCCAGGCTGATTTCGAACTCCTGACTTCAGCTGATC TTTAATAGAGACGGAGTTTCCCCATGTTGGCCGGGCTGATTTCGAACTCCTGACTTCAGCTGATC T C NOL6 Ensembl:ENSG00000165271 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1024532712 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78268,RMVar_hsa_circ_256387 9906 RMVar_ID_9906 Human_SNP_ID_396794900 A-to-I Human chr9 + 33580552 33580552 33580552 ACCCACCAACAGCTTGCCCCCTCAATGTGGGAAAGCTACAGACACTCAACACCAGCCCCATCCAT ACCCACCAACAGCTTGCCCCCTCAATGTGGGAGAGCTACAGACACTCAACACCAGCCCCATCCAT A G RF00017-071 RNACentral:URS00009310A4 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1323024831 Functional Loss SNV dbSNP153 33..33 33 - - - 9907 RMVar_ID_9907 Human_SNP_ID_396797261 A-to-I Human chr9 + 33589710 33589710 33589710 GAAGCTTTTCCAACAGACAGAGCCTCATGGTAAACCTCTACAAGGATGGTATAGAAGGAACATAT GAAGCTTTTCCAACAGACAGAGCCTCATGGTATACCTCTACAAGGATGGTATAGAAGGAACATAT A T CYP4F26P Ensembl:ENSG00000226562 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1290517540 Functional Loss SNV dbSNP153 33..33 33 - - - 9908 RMVar_ID_9908 Human_SNP_ID_396797275 A-to-I Human chr9 + 33589793 33589779 33589794 CTGGGAGGCACCATTTTCCAGACCCCAGATTCATAGACCCACCAACAGCTTGCACCCTTAGTGTT CTGGGAGGCACCATTTTCC_______________AGACCCACCAACAGCTTGCACCCTTAGTGTT CAGACCCCAGATTCAT C CYP4F26P Ensembl:ENSG00000226562 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs896865112 Functional Loss DEL dbSNP153 20..34 33 - - - 9909 RMVar_ID_9909 Human_SNP_ID_396797295 A-to-I Human chr9 + 33589844 33589844 33589844 GCACCCTTAGTGTTAAAAAGCTGCTGGCACTCAACAGCAGCCCAGCCCATGAGGGCAGCTTTGGG GCACCCTTAGTGTTAAAAAGCTGCTGGCACTCCACAGCAGCCCAGCCCATGAGGGCAGCTTTGGG A C CYP4F26P Ensembl:ENSG00000226562 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs575257945 Functional Loss SNV dbSNP153 33..33 33 - - - 9910 RMVar_ID_9910 Human_SNP_ID_396797949 A-to-I Human chr9 + 33592393 33592393 33592393 AAAAAGAAAACCTGATTTTCGTGGGAAAATCTAAGAGAGCTTCAGAAATTTGTATAAAATGGAGT AAAAAGAAAACCTGATTTTCGTGGGAAAATCTGAGAGAGCTTCAGAAATTTGTATAAAATGGAGT A G CYP4F26P Ensembl:ENSG00000226562 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1372794548 Functional Loss SNV dbSNP153 33..33 33 - - - 9911 RMVar_ID_9911 Human_SNP_ID_396798716 A-to-I Human chr9 + 33595429 33595428 33595429 AAAATTTGCAGCCTGGCCAAGTGGTCAAAAAGAAAAGCTGAATTTCAGGGGAAAAATTCAGGAAG AAAATTTGCAGCCTGGCCAAGTGGTCAAAAAG_AAAGCTGAATTTCAGGGGAAAAATTCAGGAAG GA G CYP4F26P Ensembl:ENSG00000226562 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1265213345 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_8276178 9912 RMVar_ID_9912 Human_SNP_ID_396798740 A-to-I Human chr9 + 33595497 33595497 33595497 TCAGAAACTTGCATGAAAAGGAGCCCAGTGCTAATAGCCAAGACAATAGGGAAAAGCCCTTGACG TCAGAAACTTGCATGAAAAGGAGCCCAGTGCTCATAGCCAAGACAATAGGGAAAAGCCCTTGACG A C CYP4F26P Ensembl:ENSG00000226562 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1489884727 Functional Loss SNV dbSNP153 33..33 33 - - - 9913 RMVar_ID_9913 Human_SNP_ID_396798745 A-to-I Human chr9 + 33595518 33595518 33595518 AGCCCAGTGCTAATAGCCAAGACAATAGGGAAAAGCCCTTGACGGCATTTTGGAGACCTTTGCAG AGCCCAGTGCTAATAGCCAAGACAATAGGGAAGAGCCCTTGACGGCATTTTGGAGACCTTTGCAG A G CYP4F26P Ensembl:ENSG00000226562 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1259388405 Functional Loss SNV dbSNP153 33..33 33 - - - 9914 RMVar_ID_9914 Human_SNP_ID_396798835 A-to-I Human chr9 + 33595880 33595880 33595880 CAGATAAAAGCATCCCAAAAATGCAGAGCCTCATAAGAAACCTCTACTAGGGCAGTGCAGAAGGA CAGATAAAAGCATCCCAAAAATGCAGAGCCTCGTAAGAAACCTCTACTAGGGCAGTGCAGAAGGA A G CYP4F26P Ensembl:ENSG00000226562 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1180900490 Functional Loss SNV dbSNP153 33..33 33 - - - 9915 RMVar_ID_9915 Human_SNP_ID_396799591 A-to-I Human chr9 + 33598799 33598799 33598799 CCGGATAGATGGTCACAGTCTATGGGCTGCACAGGATGAGGAAGCCAGAGAACAGGCAAGGTGGG CCGGATAGATGGTCACAGTCTATGGGCTGCACCGGATGAGGAAGCCAGAGAACAGGCAAGGTGGG A C CYP4F26P Ensembl:ENSG00000226562 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs543830757 Functional Loss SNV dbSNP153 33..33 33 - - - 9916 RMVar_ID_9916 Human_SNP_ID_396799596 A-to-I Human chr9 + 33598824 33598824 33598824 GCTGCACAGGATGAGGAAGCCAGAGAACAGGCAAGGTGGGCAGCAGGGGTGCAGGGAGAGGCAGG GCTGCACAGGATGAGGAAGCCAGAGAACAGGCCAGGTGGGCAGCAGGGGTGCAGGGAGAGGCAGG A C CYP4F26P Ensembl:ENSG00000226562 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1443171107 Functional Loss SNV dbSNP153 33..33 33 - - - 9917 RMVar_ID_9917 Human_SNP_ID_396799813 A-to-I Human chr9 + 33599508 33599508 33599508 TCCTGTCTCAGGACTCAGAAAGTCCAGTCCTGAGATGGGACAGTGCTCCCCAGGGTGGGTGGCCA TCCTGTCTCAGGACTCAGAAAGTCCAGTCCTGGGATGGGACAGTGCTCCCCAGGGTGGGTGGCCA A G CYP4F26P Ensembl:ENSG00000226562 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs796705602 Functional Loss SNV dbSNP153 33..33 33 - - - 9918 RMVar_ID_9918 Human_SNP_ID_396799866 A-to-I Human chr9 + 33599649 33599649 33599649 AGTGCATTGAGGTTGCACCTGGAGCCCACTCCAACTGATGCCCCCACAGCCCTCACAGGGTCTGA AGTGCATTGAGGTTGCACCTGGAGCCCACTCCGACTGATGCCCCCACAGCCCTCACAGGGTCTGA A G CYP4F26P Ensembl:ENSG00000226562 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946898143 Functional Loss SNV dbSNP153 33..33 33 - - - 9919 RMVar_ID_9919 Human_SNP_ID_396799875 A-to-I Human chr9 + 33599671 33599671 33599671 AGCCCACTCCAACTGATGCCCCCACAGCCCTCACAGGGTCTGACCTCCCAGCATGCACCTGCCTC AGCCCACTCCAACTGATGCCCCCACAGCCCTCGCAGGGTCTGACCTCCCAGCATGCACCTGCCTC A G CYP4F26P Ensembl:ENSG00000226562 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924034647 Functional Loss SNV dbSNP153 33..33 33 - - - 9920 RMVar_ID_9920 Human_SNP_ID_396806520 A-to-I Human chr9 + 33624860 33624860 33624860 CATTGATTATGAACTGATTGACCAAGATGCCCAGGATCTCTATGACGCTGGAGTGAAGAGGAAAG CATTGATTATGAACTGATTGACCAAGATGCCCGGGATCTCTATGACGCTGGAGTGAAGAGGAAAG A G ANXA2P2 Ensembl:ENSG00000231991 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs758587386 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1826107,Human_miRNA_ID_1866670,Human_miRNA_ID_1866950,Human_miRNA_ID_1904539 9921 RMVar_ID_9921 Human_SNP_ID_396818204 A-to-I Human chr9 - 33676404 33676404 33676404 TGAAAGACATTATGACACCGCCAAATCTAATTACAGAGTTGCGCAATATCCTTTTGAAGACCATA TGAAAGACATTATGACACCGCCAAATCTAATTGCAGAGTTGCGCAATATCCTTTTGAAGACCATA T C PTENP1 Ensembl:ENSG00000237984 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1166729043 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5634448,Human_RBP_ID_22411910 RMVar_hsa_circ_265675 9922 RMVar_ID_9922 Human_SNP_ID_396853702 A-to-I Human chr9 + 33825345 33825345 33825345 CTCACTGCAGCCTCCATCTCCTGGGTCCAAGCAATTCTCCTCCTCAGCTTCCCGAGTAGCTGGGG CTCACTGCAGCCTCCATCTCCTGGGTCCAAGCCATTCTCCTCCTCAGCTTCCCGAGTAGCTGGGG A C UBE2R2 Ensembl:ENSG00000107341 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs894742853 Functional Loss SNV dbSNP153 33..33 33 - - - 9923 RMVar_ID_9923 Human_SNP_ID_396854091 A-to-I Human chr9 + 33826962 33826962 33826962 AAAATTAGCCAGGCATGATGTCGTGAACCTGTAGTCCCAGCTATCCGAGAGGCTGAAGCAGGAGA AAAATTAGCCAGGCATGATGTCGTGAACCTGTGGTCCCAGCTATCCGAGAGGCTGAAGCAGGAGA A G UBE2R2 Ensembl:ENSG00000107341 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs905953480 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16658312,Human_RBP_ID_17579635,Human_RBP_ID_23316672 9924 RMVar_ID_9924 Human_SNP_ID_396855521 A-to-I Human chr9 + 33831789 33831789 33831789 TCATGCCATTCTCCTGCCTCAGCCTCCCTAGTAGTTGGGACTATAGGTGCCTGCCAACACGCCCG TCATGCCATTCTCCTGCCTCAGCCTCCCTAGTGGTTGGGACTATAGGTGCCTGCCAACACGCCCG A G UBE2R2 Ensembl:ENSG00000107341 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1435024133 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7922280,Human_RBP_ID_16658375 9925 RMVar_ID_9925 Human_SNP_ID_396856329 A-to-I Human chr9 + 33834473 33834473 33834473 ACCTTAGGTGATCTGCCCACCTTGGCCTCCCAAAGTGTTGGGATTACAGGCGTGAGCCACACGCC ACCTTAGGTGATCTGCCCACCTTGGCCTCCCATAGTGTTGGGATTACAGGCGTGAGCCACACGCC A T UBE2R2 Ensembl:ENSG00000107341 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs766485320 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16658410 9926 RMVar_ID_9926 Human_SNP_ID_396856431 A-to-I Human chr9 + 33834854 33834848 33834855 ATCCCTTGTTCCCGGGAGGTGGAGGTTGCAGTAAGCCGAGATCGTGCCGTTGCACTCCAGCCTGG ATCCCTTGTTCCCGGGAGGTGGAGGTT_______GCCGAGATCGTGCCGTTGCACTCCAGCCTGG TGCAGTAA T UBE2R2 Ensembl:ENSG00000107341 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1199001806 Functional Loss DEL dbSNP153 28..34 33 - - - Human_RBP_ID_23316676 9927 RMVar_ID_9927 Human_SNP_ID_396856434 A-to-I Human chr9 + 33834854 33834854 33834854 ATCCCTTGTTCCCGGGAGGTGGAGGTTGCAGTAAGCCGAGATCGTGCCGTTGCACTCCAGCCTGG ATCCCTTGTTCCCGGGAGGTGGAGGTTGCAGTGAGCCGAGATCGTGCCGTTGCACTCCAGCCTGG A G UBE2R2 Ensembl:ENSG00000107341 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1563983042 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23316676 9928 RMVar_ID_9928 Human_SNP_ID_396856611 A-to-I Human chr9 + 33835327 33835327 33835327 CACCACCATGCCTGGGTAATTTTTGTATTTTTAGTAGATACAAGGTTTCATCATATTGGTCAGGC CACCACCATGCCTGGGTAATTTTTGTATTTTTGGTAGATACAAGGTTTCATCATATTGGTCAGGC A G UBE2R2 Ensembl:ENSG00000107341 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs530487953 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16658413,Human_RBP_ID_23201164 9929 RMVar_ID_9929 Human_SNP_ID_396857194 A-to-I Human chr9 + 33837598 33837598 33837598 TAGGCACCTGCTACCACACCCAGCTAATTTTTATATTTTTAGTAGAGATGGGTTTTGCTGTGTTG TAGGCACCTGCTACCACACCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGTTTTGCTGTGTTG A G UBE2R2 Ensembl:ENSG00000107341 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs939271163 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_184414 9930 RMVar_ID_9930 Human_SNP_ID_396857213 A-to-I Human chr9 + 33837668 33837668 33837668 GCTGTTCTTGAACTCCTGAGCTCAATTGATCTACCTGCCTTAGCCTCTCATTGTGCTAGGATTAC GCTGTTCTTGAACTCCTGAGCTCAATTGATCTGCCTGCCTTAGCCTCTCATTGTGCTAGGATTAC A G UBE2R2 Ensembl:ENSG00000107341 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1007674808 Functional Loss SNV dbSNP153 33..33 33 - - - 9931 RMVar_ID_9931 Human_SNP_ID_396857218 A-to-I Human chr9 + 33837693 33837693 33837693 TTGATCTACCTGCCTTAGCCTCTCATTGTGCTAGGATTACAGAGCCACCACACCTGGCCTGTTCT TTGATCTACCTGCCTTAGCCTCTCATTGTGCTGGGATTACAGAGCCACCACACCTGGCCTGTTCT A G UBE2R2 Ensembl:ENSG00000107341 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1482463549 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8703606,Human_RBP_ID_16658486 9932 RMVar_ID_9932 Human_SNP_ID_396857627 A-to-I Human chr9 + 33839268 33839268 33839268 GTGTTTTTGTTTTTGTTTTGAGACGGAGTTTCACTCTTGTTGCCCAGACTGGACTGCAATGGCAG GTGTTTTTGTTTTTGTTTTGAGACGGAGTTTCGCTCTTGTTGCCCAGACTGGACTGCAATGGCAG A G UBE2R2 Ensembl:ENSG00000107341 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1366306132 Functional Loss SNV dbSNP153 33..33 33 - - - 9933 RMVar_ID_9933 Human_SNP_ID_396857656 A-to-I Human chr9 + 33839376 33839376 33839376 TCTCCTGCCTCAGCCTCCCAGGTAGCTGAGATAACAGGCTCCTGCCACCACACCTGGCTAATTTT TCTCCTGCCTCAGCCTCCCAGGTAGCTGAGATTACAGGCTCCTGCCACCACACCTGGCTAATTTT A T UBE2R2 Ensembl:ENSG00000107341 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs13295956 Functional Loss SNV dbSNP153 33..33 33 - - - 9934 RMVar_ID_9934 Human_SNP_ID_396857692 A-to-I Human chr9 + 33839499 33839499 33839499 ACCTCAGGTGATCCACCCGCCTCAGCCTTCCAAAGTGCTGGGAGTACAGGTGTGAGCCACCGTGC ACCTCAGGTGATCCACCCGCCTCAGCCTTCCAGAGTGCTGGGAGTACAGGTGTGAGCCACCGTGC A G UBE2R2 Ensembl:ENSG00000107341 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1047885819 Functional Loss SNV dbSNP153 33..33 33 - - - 9935 RMVar_ID_9935 Human_SNP_ID_396857737 A-to-I Human chr9 + 33839738 33839738 33839738 GTTGTTTAAGCTAGGAGTGGTGGCTCATGCCTATAATCCTAGCACTTTGGGAGGCTGAGGTGGGA GTTGTTTAAGCTAGGAGTGGTGGCTCATGCCTGTAATCCTAGCACTTTGGGAGGCTGAGGTGGGA A G UBE2R2 Ensembl:ENSG00000107341 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs960155535 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26220142 9936 RMVar_ID_9936 Human_SNP_ID_396857749 A-to-I Human chr9 + 33839786 33839786 33839786 GGGAGGCTGAGGTGGGAAGATTGCTTGAGATCAGGAGTTTAAGACCAGCCTGGGCAACATAGCAA GGGAGGCTGAGGTGGGAAGATTGCTTGAGATCGGGAGTTTAAGACCAGCCTGGGCAACATAGCAA A G UBE2R2 Ensembl:ENSG00000107341 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1368440524 Functional Loss SNV dbSNP153 33..33 33 - - - 9937 RMVar_ID_9937 Human_SNP_ID_396858501 A-to-I Human chr9 + 33842918 33842918 33842918 TATTCTAGCCACATGCCATGACACATGCCTGTAGTTCCAGCTACTTGGAAGGCTGAGGTGGGAGG TATTCTAGCCACATGCCATGACACATGCCTGTTGTTCCAGCTACTTGGAAGGCTGAGGTGGGAGG A T UBE2R2 Ensembl:ENSG00000107341 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1218828985 Functional Loss SNV dbSNP153 33..33 33 - - - 9938 RMVar_ID_9938 Human_SNP_ID_396859304 A-to-I Human chr9 + 33845739 33845739 33845739 CTTCATTTAGAATTTTCTAGGCCGGGTACAGTAGCTCACGCCTGTAATCCCAGCACTTTGGGAGG CTTCATTTAGAATTTTCTAGGCCGGGTACAGTTGCTCACGCCTGTAATCCCAGCACTTTGGGAGG A T UBE2R2 Ensembl:ENSG00000107341 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1230917756 Functional Loss SNV dbSNP153 33..33 33 - - - 9939 RMVar_ID_9939 Human_SNP_ID_396859466 A-to-I Human chr9 + 33846175 33846175 33846175 AAAATTAGCCAGGTGTGGTGGCACGAGCCTGTAATCCCAACTTCTTGGGAGGCTCAGGCAGGGGA AAAATTAGCCAGGTGTGGTGGCACGAGCCTGTTATCCCAACTTCTTGGGAGGCTCAGGCAGGGGA A T UBE2R2 Ensembl:ENSG00000107341 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1416398004 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16658689 9940 RMVar_ID_9940 Human_SNP_ID_396859472 A-to-I Human chr9 + 33846207 33846207 33846207 AATCCCAACTTCTTGGGAGGCTCAGGCAGGGGAATCACTTGAACCCAGGAAGCAGAGGTTGCTCT AATCCCAACTTCTTGGGAGGCTCAGGCAGGGGCATCACTTGAACCCAGGAAGCAGAGGTTGCTCT A C UBE2R2 Ensembl:ENSG00000107341 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs571862448 Functional Loss SNV dbSNP153 33..33 33 - - - 9941 RMVar_ID_9941 Human_SNP_ID_396861384 A-to-I Human chr9 + 33853905 33853905 33853905 TTTTGTGGAGTCCAGATCTTGCTGTGTTTCTCAGGCTGGTCTCAAGCTCTTGGGCTCAAGCCATC TTTTGTGGAGTCCAGATCTTGCTGTGTTTCTCGGGCTGGTCTCAAGCTCTTGGGCTCAAGCCATC A G UBE2R2 Ensembl:ENSG00000107341 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1319697754 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24392339 9942 RMVar_ID_9942 Human_SNP_ID_396861542 A-to-I Human chr9 + 33854561 33854561 33854561 CCAGTTTGGTCTTGAACTCCTGACTTTACGTGATCCGCCTGCTTCGGCCTCCCAAGGTGCTGGGA CCAGTTTGGTCTTGAACTCCTGACTTTACGTGGTCCGCCTGCTTCGGCCTCCCAAGGTGCTGGGA A G UBE2R2 Ensembl:ENSG00000107341 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs759674087 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16658888 9943 RMVar_ID_9943 Human_SNP_ID_396866771 A-to-I Human chr9 + 33874047 33874047 33874047 TCCGCTCACTGTAACCTCTGCTTCCCGAGTTCAAGCAATTCTCCTGTCTCAGCCGCCCAAGTAGC TCCGCTCACTGTAACCTCTGCTTCCCGAGTTCGAGCAATTCTCCTGTCTCAGCCGCCCAAGTAGC A G UBE2R2 Ensembl:ENSG00000107341 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947577409 Functional Loss SNV dbSNP153 33..33 33 - - - 9944 RMVar_ID_9944 Human_SNP_ID_396868229 A-to-I Human chr9 + 33879553 33879553 33879553 ACAGCTTACTGCAGACTCGACCTCCTGGGCTCAGGTGATTTTCCCACCTCAGCCTCCTGAGTAGC ACAGCTTACTGCAGACTCGACCTCCTGGGCTCGGGTGATTTTCCCACCTCAGCCTCCTGAGTAGC A G UBE2R2 Ensembl:ENSG00000107341 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903064089 Functional Loss SNV dbSNP153 33..33 33 - - - 9945 RMVar_ID_9945 Human_SNP_ID_396870449 A-to-I Human chr9 + 33888706 33888706 33888706 ACCTGGCTAATTTTTGTATTTTTAGCAGAGACAGTGTTTCACCATGTCGGCCAGAGTGGCCTCGA ACCTGGCTAATTTTTGTATTTTTAGCAGAGACCGTGTTTCACCATGTCGGCCAGAGTGGCCTCGA A C UBE2R2 Ensembl:ENSG00000107341 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1419614971 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_276361,RMVar_hsa_circ_256400,RMVar_hsa_circ_271389,RMVar_hsa_circ_256399 9946 RMVar_ID_9946 Human_SNP_ID_396870824 A-to-I Human chr9 + 33890327 33890327 33890327 GAAGTGATAGGCCGGGCGCAGTGGCTCACCCTATAATCCCAGCACTTTGGAAGGCTGAGTTGAGG GAAGTGATAGGCCGGGCGCAGTGGCTCACCCTGTAATCCCAGCACTTTGGAAGGCTGAGTTGAGG A G UBE2R2 Ensembl:ENSG00000107341 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1232190658 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_276361,RMVar_hsa_circ_256400,RMVar_hsa_circ_271389,RMVar_hsa_circ_256399 9947 RMVar_ID_9947 Human_SNP_ID_396871261 A-to-I Human chr9 + 33891852 33891852 33891852 TTGTTGTTGGCTGGGCACAGTGGCTTATGCCTATAATCCCAGCACTTTGGGAGGCTGAGGCAAGT TTGTTGTTGGCTGGGCACAGTGGCTTATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAAGT A G UBE2R2 Ensembl:ENSG00000107341 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs982362596 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_276361,RMVar_hsa_circ_256400,RMVar_hsa_circ_271389,RMVar_hsa_circ_256399 9948 RMVar_ID_9948 Human_SNP_ID_396875513 A-to-I Human chr9 + 33909621 33909619 33909622 CTTGAGCCCAGGAGTAGAGACGGGGTTTCACCATGTTAGCCAGGATGGTCTCGATCTCCTTACCT CTTGAGCCCAGGAGTAGAGACGGGGTTTCAC___GTTAGCCAGGATGGTCTCGATCTCCTTACCT CCAT C UBE2R2 Ensembl:ENSG00000107341 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1425287007 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_276361,RMVar_hsa_circ_256400,RMVar_hsa_circ_256401,RMVar_hsa_circ_269972,RMVar_hsa_circ_256402 9949 RMVar_ID_9949 Human_SNP_ID_396875515 A-to-I Human chr9 + 33909621 33909621 33909621 CTTGAGCCCAGGAGTAGAGACGGGGTTTCACCATGTTAGCCAGGATGGTCTCGATCTCCTTACCT CTTGAGCCCAGGAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGGTCTCGATCTCCTTACCT A G UBE2R2 Ensembl:ENSG00000107341 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs911925343 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_276361,RMVar_hsa_circ_256400,RMVar_hsa_circ_256401,RMVar_hsa_circ_269972,RMVar_hsa_circ_256402 9950 RMVar_ID_9950 Human_SNP_ID_396876762 A-to-I Human chr9 + 33914662 33914662 33914662 CAACCTGGCCAACATGGTGAAATCCCATCTCTACCAAAAAATATAAAAGTTAGTTGGGCATAGTG CAACCTGGCCAACATGGTGAAATCCCATCTCTCCCAAAAAATATAAAAGTTAGTTGGGCATAGTG A C UBE2R2 Ensembl:ENSG00000107341 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1328155615 Functional Loss SNV dbSNP153 33..33 33 - - - 9951 RMVar_ID_9951 Human_SNP_ID_396882981 A-to-I Human chr9 - 33936171 33936171 33936171 GGAGACCAGCCTGGTCAACATGGCAAAACCCCATCTCTACAGAAAATACAAGAATTAGCTAGGCA GGAGACCAGCCTGGTCAACATGGCAAAACCCCGTCTCTACAGAAAATACAAGAATTAGCTAGGCA T C UBAP2 Ensembl:ENSG00000137073 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs536149114 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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 9952 RMVar_ID_9952 Human_SNP_ID_396882982 A-to-I Human chr9 - 33936171 33936171 33936171 GGAGACCAGCCTGGTCAACATGGCAAAACCCCATCTCTACAGAAAATACAAGAATTAGCTAGGCA GGAGACCAGCCTGGTCAACATGGCAAAACCCCCTCTCTACAGAAAATACAAGAATTAGCTAGGCA T G UBAP2 Ensembl:ENSG00000137073 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs536149114 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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 9953 RMVar_ID_9953 Human_SNP_ID_396886773 A-to-I Human chr9 - 33949042 33949042 33949042 CTGCCTCAGTCTCCCGAGTAGCTGGGACTACAAGCGCCTGCCAAAACTCCCGGCTAATTTTTTTG CTGCCTCAGTCTCCCGAGTAGCTGGGACTACATGCGCCTGCCAAAACTCCCGGCTAATTTTTTTG T A UBAP2 Ensembl:ENSG00000137073 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1292103792 Functional Loss SNV dbSNP153 33..33 33 - - - 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_19793,RMVar_hsa_circ_3151,RMVar_hsa_circ_89057,RMVar_hsa_circ_256411,RMVar_hsa_circ_125190,RMVar_hsa_circ_112891,RMVar_hsa_circ_256412,RMVar_hsa_circ_256413,RMVar_hsa_circ_256414,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_256422,RMVar_hsa_circ_116561,RMVar_hsa_circ_369653,RMVar_hsa_circ_114511,RMVar_hsa_circ_84253,RMVar_hsa_circ_256433,RMVar_hsa_circ_256425,RMVar_hsa_circ_256426,RMVar_hsa_circ_256423,RMVar_hsa_circ_256424,RMVar_hsa_circ_318165,RMVar_hsa_circ_374778,RMVar_hsa_circ_316868,RMVar_hsa_circ_288073,RMVar_hsa_circ_289056,RMVar_hsa_circ_256435,RMVar_hsa_circ_256436,RMVar_hsa_circ_256434,RMVar_hsa_circ_61227,RMVar_hsa_circ_361931,RMVar_hsa_circ_289968,RMVar_hsa_circ_47856,RMVar_hsa_circ_256437,RMVar_hsa_circ_368802,RMVar_hsa_circ_281300,RMVar_hsa_circ_283459,RMVar_hsa_circ_38224,RMVar_hsa_circ_280058,RMVar_hsa_circ_256438,RMVar_hsa_circ_256440,RMVar_hsa_circ_256439,RMVar_hsa_circ_298663,RMVar_hsa_circ_302696,RMVar_hsa_circ_323255,RMVar_hsa_circ_300254,RMVar_hsa_circ_294493,RMVar_hsa_circ_270766,RMVar_hsa_circ_277730,RMVar_hsa_circ_256445,RMVar_hsa_circ_256447,RMVar_hsa_circ_256448,RMVar_hsa_circ_256446,RMVar_hsa_circ_256443,RMVar_hsa_circ_256444 9954 RMVar_ID_9954 Human_SNP_ID_396889356 A-to-I Human chr9 - 33958539 33958539 33958539 GCCAGGTGGGATGGTGGGCACCTGTAATTCCAATTACTTGGGAGACTGAGGCAGGAGAATCACTT GCCAGGTGGGATGGTGGGCACCTGTAATTCCAGTTACTTGGGAGACTGAGGCAGGAGAATCACTT T C UBAP2 Ensembl:ENSG00000137073 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1411274966 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121448,RMVar_hsa_circ_127395,RMVar_hsa_circ_106612,RMVar_hsa_circ_256406,RMVar_hsa_circ_256407,RMVar_hsa_circ_256408,RMVar_hsa_circ_110369,RMVar_hsa_circ_19793,RMVar_hsa_circ_3151,RMVar_hsa_circ_256411,RMVar_hsa_circ_125190,RMVar_hsa_circ_112891,RMVar_hsa_circ_256412,RMVar_hsa_circ_256413,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_369653,RMVar_hsa_circ_114511,RMVar_hsa_circ_84253,RMVar_hsa_circ_256425,RMVar_hsa_circ_256426,RMVar_hsa_circ_256423,RMVar_hsa_circ_256424,RMVar_hsa_circ_318165,RMVar_hsa_circ_374778,RMVar_hsa_circ_288073,RMVar_hsa_circ_256435,RMVar_hsa_circ_256436,RMVar_hsa_circ_61227,RMVar_hsa_circ_47856,RMVar_hsa_circ_368802,RMVar_hsa_circ_256450,RMVar_hsa_circ_125526,RMVar_hsa_circ_38224,RMVar_hsa_circ_256438,RMVar_hsa_circ_298663,RMVar_hsa_circ_302696,RMVar_hsa_circ_323255,RMVar_hsa_circ_300254,RMVar_hsa_circ_294493,RMVar_hsa_circ_270766,RMVar_hsa_circ_256445,RMVar_hsa_circ_256447,RMVar_hsa_circ_256448,RMVar_hsa_circ_256446,RMVar_hsa_circ_276368,RMVar_hsa_circ_334323,RMVar_hsa_circ_365844,RMVar_hsa_circ_286942,RMVar_hsa_circ_305118,RMVar_hsa_circ_284193,RMVar_hsa_circ_274043,RMVar_hsa_circ_271964,RMVar_hsa_circ_256454,RMVar_hsa_circ_256458,RMVar_hsa_circ_87464,RMVar_hsa_circ_256456,RMVar_hsa_circ_256457,RMVar_hsa_circ_256455,RMVar_hsa_circ_256452,RMVar_hsa_circ_256453,RMVar_hsa_circ_256451,RMVar_hsa_circ_256461,RMVar_hsa_circ_297740,RMVar_hsa_circ_362765,RMVar_hsa_circ_374877,RMVar_hsa_circ_256449,RMVar_hsa_circ_366282,RMVar_hsa_circ_310332,RMVar_hsa_circ_56216,RMVar_hsa_circ_275162,RMVar_hsa_circ_256462,RMVar_hsa_circ_256463,RMVar_hsa_circ_256464,RMVar_hsa_circ_256465 9955 RMVar_ID_9955 Human_SNP_ID_396889489 A-to-I Human chr9 - 33958979 33958979 33958979 ATGCCTGGCCAATGTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGGTCTC ATGCCTGGCCAATGTTTGTATTTTTAGTAGAGGCGGGGTTTCACCATGTTGGCCAGGCTGGTCTC T C UBAP2 Ensembl:ENSG00000137073 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs560298322 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121448,RMVar_hsa_circ_127395,RMVar_hsa_circ_106612,RMVar_hsa_circ_256406,RMVar_hsa_circ_256407,RMVar_hsa_circ_256408,RMVar_hsa_circ_110369,RMVar_hsa_circ_19793,RMVar_hsa_circ_3151,RMVar_hsa_circ_256411,RMVar_hsa_circ_125190,RMVar_hsa_circ_112891,RMVar_hsa_circ_256412,RMVar_hsa_circ_256413,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_369653,RMVar_hsa_circ_114511,RMVar_hsa_circ_84253,RMVar_hsa_circ_256425,RMVar_hsa_circ_256426,RMVar_hsa_circ_256423,RMVar_hsa_circ_256424,RMVar_hsa_circ_318165,RMVar_hsa_circ_374778,RMVar_hsa_circ_288073,RMVar_hsa_circ_256435,RMVar_hsa_circ_256436,RMVar_hsa_circ_61227,RMVar_hsa_circ_47856,RMVar_hsa_circ_368802,RMVar_hsa_circ_256450,RMVar_hsa_circ_125526,RMVar_hsa_circ_38224,RMVar_hsa_circ_256438,RMVar_hsa_circ_298663,RMVar_hsa_circ_302696,RMVar_hsa_circ_323255,RMVar_hsa_circ_300254,RMVar_hsa_circ_294493,RMVar_hsa_circ_270766,RMVar_hsa_circ_256445,RMVar_hsa_circ_256447,RMVar_hsa_circ_256448,RMVar_hsa_circ_256446,RMVar_hsa_circ_276368,RMVar_hsa_circ_334323,RMVar_hsa_circ_365844,RMVar_hsa_circ_286942,RMVar_hsa_circ_305118,RMVar_hsa_circ_284193,RMVar_hsa_circ_274043,RMVar_hsa_circ_271964,RMVar_hsa_circ_256454,RMVar_hsa_circ_256458,RMVar_hsa_circ_87464,RMVar_hsa_circ_256456,RMVar_hsa_circ_256457,RMVar_hsa_circ_256455,RMVar_hsa_circ_256452,RMVar_hsa_circ_256453,RMVar_hsa_circ_256451,RMVar_hsa_circ_256461,RMVar_hsa_circ_297740,RMVar_hsa_circ_362765,RMVar_hsa_circ_374877,RMVar_hsa_circ_256449,RMVar_hsa_circ_366282,RMVar_hsa_circ_310332,RMVar_hsa_circ_56216,RMVar_hsa_circ_275162,RMVar_hsa_circ_256462,RMVar_hsa_circ_256463,RMVar_hsa_circ_256464,RMVar_hsa_circ_256465 9956 RMVar_ID_9956 Human_SNP_ID_396889493 A-to-I Human chr9 - 33959001 33959001 33959001 GGAATTATAGATGCACGCCACCATGCCTGGCCAATGTTTGTATTTTTAGTAGAGACGGGGTTTCA GGAATTATAGATGCACGCCACCATGCCTGGCCGATGTTTGTATTTTTAGTAGAGACGGGGTTTCA T C UBAP2 Ensembl:ENSG00000137073 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs182011889 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121448,RMVar_hsa_circ_127395,RMVar_hsa_circ_106612,RMVar_hsa_circ_256406,RMVar_hsa_circ_256407,RMVar_hsa_circ_256408,RMVar_hsa_circ_110369,RMVar_hsa_circ_19793,RMVar_hsa_circ_3151,RMVar_hsa_circ_256411,RMVar_hsa_circ_125190,RMVar_hsa_circ_112891,RMVar_hsa_circ_256412,RMVar_hsa_circ_256413,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_369653,RMVar_hsa_circ_114511,RMVar_hsa_circ_84253,RMVar_hsa_circ_256425,RMVar_hsa_circ_256426,RMVar_hsa_circ_256423,RMVar_hsa_circ_256424,RMVar_hsa_circ_318165,RMVar_hsa_circ_374778,RMVar_hsa_circ_288073,RMVar_hsa_circ_256435,RMVar_hsa_circ_256436,RMVar_hsa_circ_61227,RMVar_hsa_circ_47856,RMVar_hsa_circ_368802,RMVar_hsa_circ_256450,RMVar_hsa_circ_125526,RMVar_hsa_circ_38224,RMVar_hsa_circ_256438,RMVar_hsa_circ_298663,RMVar_hsa_circ_302696,RMVar_hsa_circ_323255,RMVar_hsa_circ_300254,RMVar_hsa_circ_294493,RMVar_hsa_circ_270766,RMVar_hsa_circ_256445,RMVar_hsa_circ_256447,RMVar_hsa_circ_256448,RMVar_hsa_circ_256446,RMVar_hsa_circ_276368,RMVar_hsa_circ_334323,RMVar_hsa_circ_365844,RMVar_hsa_circ_286942,RMVar_hsa_circ_305118,RMVar_hsa_circ_284193,RMVar_hsa_circ_274043,RMVar_hsa_circ_271964,RMVar_hsa_circ_256454,RMVar_hsa_circ_256458,RMVar_hsa_circ_87464,RMVar_hsa_circ_256456,RMVar_hsa_circ_256457,RMVar_hsa_circ_256455,RMVar_hsa_circ_256452,RMVar_hsa_circ_256453,RMVar_hsa_circ_256451,RMVar_hsa_circ_256461,RMVar_hsa_circ_297740,RMVar_hsa_circ_362765,RMVar_hsa_circ_374877,RMVar_hsa_circ_256449,RMVar_hsa_circ_366282,RMVar_hsa_circ_310332,RMVar_hsa_circ_56216,RMVar_hsa_circ_275162,RMVar_hsa_circ_256462,RMVar_hsa_circ_256463,RMVar_hsa_circ_256464,RMVar_hsa_circ_256465 9957 RMVar_ID_9957 Human_SNP_ID_396889502 A-to-I Human chr9 - 33959037 33959037 33959037 TCAAGTGATTCTCCTGCCCCAGCCACCTGAGTAGCTGGAATTATAGATGCACGCCACCATGCCTG TCAAGTGATTCTCCTGCCCCAGCCACCTGAGTGGCTGGAATTATAGATGCACGCCACCATGCCTG T C UBAP2 Ensembl:ENSG00000137073 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1564030930 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121448,RMVar_hsa_circ_127395,RMVar_hsa_circ_106612,RMVar_hsa_circ_256406,RMVar_hsa_circ_256407,RMVar_hsa_circ_256408,RMVar_hsa_circ_110369,RMVar_hsa_circ_19793,RMVar_hsa_circ_3151,RMVar_hsa_circ_256411,RMVar_hsa_circ_125190,RMVar_hsa_circ_112891,RMVar_hsa_circ_256412,RMVar_hsa_circ_256413,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_369653,RMVar_hsa_circ_114511,RMVar_hsa_circ_84253,RMVar_hsa_circ_256425,RMVar_hsa_circ_256426,RMVar_hsa_circ_256423,RMVar_hsa_circ_256424,RMVar_hsa_circ_318165,RMVar_hsa_circ_374778,RMVar_hsa_circ_288073,RMVar_hsa_circ_256435,RMVar_hsa_circ_256436,RMVar_hsa_circ_61227,RMVar_hsa_circ_47856,RMVar_hsa_circ_368802,RMVar_hsa_circ_256450,RMVar_hsa_circ_125526,RMVar_hsa_circ_38224,RMVar_hsa_circ_256438,RMVar_hsa_circ_298663,RMVar_hsa_circ_302696,RMVar_hsa_circ_323255,RMVar_hsa_circ_300254,RMVar_hsa_circ_294493,RMVar_hsa_circ_270766,RMVar_hsa_circ_256445,RMVar_hsa_circ_256447,RMVar_hsa_circ_256448,RMVar_hsa_circ_256446,RMVar_hsa_circ_276368,RMVar_hsa_circ_334323,RMVar_hsa_circ_365844,RMVar_hsa_circ_286942,RMVar_hsa_circ_305118,RMVar_hsa_circ_284193,RMVar_hsa_circ_274043,RMVar_hsa_circ_271964,RMVar_hsa_circ_256454,RMVar_hsa_circ_256458,RMVar_hsa_circ_87464,RMVar_hsa_circ_256456,RMVar_hsa_circ_256457,RMVar_hsa_circ_256455,RMVar_hsa_circ_256452,RMVar_hsa_circ_256453,RMVar_hsa_circ_256451,RMVar_hsa_circ_256461,RMVar_hsa_circ_297740,RMVar_hsa_circ_362765,RMVar_hsa_circ_374877,RMVar_hsa_circ_256449,RMVar_hsa_circ_366282,RMVar_hsa_circ_310332,RMVar_hsa_circ_56216,RMVar_hsa_circ_275162,RMVar_hsa_circ_256462,RMVar_hsa_circ_256463,RMVar_hsa_circ_256464,RMVar_hsa_circ_256465 9958 RMVar_ID_9958 Human_SNP_ID_396889755 A-to-I Human chr9 - 33960054 33960054 33960054 GTGGGGTTGTGCATCTGTAGTCTCAGCTACTCAGGAGGCTAAGGCAGGAGGATCTCTTGAGCCCA GTGGGGTTGTGCATCTGTAGTCTCAGCTACTCGGGAGGCTAAGGCAGGAGGATCTCTTGAGCCCA T C UBAP2 Ensembl:ENSG00000137073 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs540001313 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15698,Human_RBP_ID_16660525,Human_RBP_ID_26220636 RMVar_hsa_circ_121448,RMVar_hsa_circ_127395,RMVar_hsa_circ_106612,RMVar_hsa_circ_256406,RMVar_hsa_circ_256407,RMVar_hsa_circ_256408,RMVar_hsa_circ_110369,RMVar_hsa_circ_19793,RMVar_hsa_circ_3151,RMVar_hsa_circ_256411,RMVar_hsa_circ_125190,RMVar_hsa_circ_112891,RMVar_hsa_circ_256412,RMVar_hsa_circ_256413,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_369653,RMVar_hsa_circ_114511,RMVar_hsa_circ_84253,RMVar_hsa_circ_256425,RMVar_hsa_circ_256426,RMVar_hsa_circ_256423,RMVar_hsa_circ_256424,RMVar_hsa_circ_318165,RMVar_hsa_circ_374778,RMVar_hsa_circ_288073,RMVar_hsa_circ_256435,RMVar_hsa_circ_256436,RMVar_hsa_circ_61227,RMVar_hsa_circ_47856,RMVar_hsa_circ_368802,RMVar_hsa_circ_256450,RMVar_hsa_circ_125526,RMVar_hsa_circ_38224,RMVar_hsa_circ_256438,RMVar_hsa_circ_298663,RMVar_hsa_circ_302696,RMVar_hsa_circ_323255,RMVar_hsa_circ_300254,RMVar_hsa_circ_294493,RMVar_hsa_circ_270766,RMVar_hsa_circ_256445,RMVar_hsa_circ_256447,RMVar_hsa_circ_256448,RMVar_hsa_circ_256446,RMVar_hsa_circ_276368,RMVar_hsa_circ_334323,RMVar_hsa_circ_365844,RMVar_hsa_circ_286942,RMVar_hsa_circ_305118,RMVar_hsa_circ_284193,RMVar_hsa_circ_274043,RMVar_hsa_circ_271964,RMVar_hsa_circ_256454,RMVar_hsa_circ_256458,RMVar_hsa_circ_87464,RMVar_hsa_circ_256456,RMVar_hsa_circ_256457,RMVar_hsa_circ_256455,RMVar_hsa_circ_256452,RMVar_hsa_circ_256453,RMVar_hsa_circ_256451,RMVar_hsa_circ_256461,RMVar_hsa_circ_297740,RMVar_hsa_circ_362765,RMVar_hsa_circ_374877,RMVar_hsa_circ_256449,RMVar_hsa_circ_366282,RMVar_hsa_circ_310332,RMVar_hsa_circ_56216,RMVar_hsa_circ_275162,RMVar_hsa_circ_256462,RMVar_hsa_circ_256463,RMVar_hsa_circ_256464,RMVar_hsa_circ_256465 9959 RMVar_ID_9959 Human_SNP_ID_396889760 A-to-I Human chr9 - 33960068 33960068 33960068 AAAATTACCTGGGTGTGGGGTTGTGCATCTGTAGTCTCAGCTACTCAGGAGGCTAAGGCAGGAGG AAAATTACCTGGGTGTGGGGTTGTGCATCTGTTGTCTCAGCTACTCAGGAGGCTAAGGCAGGAGG T A UBAP2 Ensembl:ENSG00000137073 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1473051815 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15698,Human_RBP_ID_16660525 RMVar_hsa_circ_121448,RMVar_hsa_circ_127395,RMVar_hsa_circ_106612,RMVar_hsa_circ_256406,RMVar_hsa_circ_256407,RMVar_hsa_circ_256408,RMVar_hsa_circ_110369,RMVar_hsa_circ_19793,RMVar_hsa_circ_3151,RMVar_hsa_circ_256411,RMVar_hsa_circ_125190,RMVar_hsa_circ_112891,RMVar_hsa_circ_256412,RMVar_hsa_circ_256413,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_369653,RMVar_hsa_circ_114511,RMVar_hsa_circ_84253,RMVar_hsa_circ_256425,RMVar_hsa_circ_256426,RMVar_hsa_circ_256423,RMVar_hsa_circ_256424,RMVar_hsa_circ_318165,RMVar_hsa_circ_374778,RMVar_hsa_circ_288073,RMVar_hsa_circ_256435,RMVar_hsa_circ_256436,RMVar_hsa_circ_61227,RMVar_hsa_circ_47856,RMVar_hsa_circ_368802,RMVar_hsa_circ_256450,RMVar_hsa_circ_125526,RMVar_hsa_circ_38224,RMVar_hsa_circ_256438,RMVar_hsa_circ_298663,RMVar_hsa_circ_302696,RMVar_hsa_circ_323255,RMVar_hsa_circ_300254,RMVar_hsa_circ_294493,RMVar_hsa_circ_270766,RMVar_hsa_circ_256445,RMVar_hsa_circ_256447,RMVar_hsa_circ_256448,RMVar_hsa_circ_256446,RMVar_hsa_circ_276368,RMVar_hsa_circ_334323,RMVar_hsa_circ_365844,RMVar_hsa_circ_286942,RMVar_hsa_circ_305118,RMVar_hsa_circ_284193,RMVar_hsa_circ_274043,RMVar_hsa_circ_271964,RMVar_hsa_circ_256454,RMVar_hsa_circ_256458,RMVar_hsa_circ_87464,RMVar_hsa_circ_256456,RMVar_hsa_circ_256457,RMVar_hsa_circ_256455,RMVar_hsa_circ_256452,RMVar_hsa_circ_256453,RMVar_hsa_circ_256451,RMVar_hsa_circ_256461,RMVar_hsa_circ_297740,RMVar_hsa_circ_362765,RMVar_hsa_circ_374877,RMVar_hsa_circ_256449,RMVar_hsa_circ_366282,RMVar_hsa_circ_310332,RMVar_hsa_circ_56216,RMVar_hsa_circ_275162,RMVar_hsa_circ_256462,RMVar_hsa_circ_256463,RMVar_hsa_circ_256464,RMVar_hsa_circ_256465 9960 RMVar_ID_9960 Human_SNP_ID_396889912 A-to-I Human chr9 - 33960704 33960704 33960704 GTGATCTTGGCTCATTGCAACCTCTGCCTCCCAGATTCAAGCAGTTCTTCTGCCTCAGCCTCCCA GTGATCTTGGCTCATTGCAACCTCTGCCTCCCCGATTCAAGCAGTTCTTCTGCCTCAGCCTCCCA T G UBAP2 Ensembl:ENSG00000137073 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1157738218 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121448,RMVar_hsa_circ_127395,RMVar_hsa_circ_106612,RMVar_hsa_circ_256406,RMVar_hsa_circ_256407,RMVar_hsa_circ_256408,RMVar_hsa_circ_110369,RMVar_hsa_circ_19793,RMVar_hsa_circ_3151,RMVar_hsa_circ_256411,RMVar_hsa_circ_125190,RMVar_hsa_circ_112891,RMVar_hsa_circ_256412,RMVar_hsa_circ_256413,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_369653,RMVar_hsa_circ_114511,RMVar_hsa_circ_84253,RMVar_hsa_circ_256425,RMVar_hsa_circ_256426,RMVar_hsa_circ_256423,RMVar_hsa_circ_256424,RMVar_hsa_circ_318165,RMVar_hsa_circ_374778,RMVar_hsa_circ_288073,RMVar_hsa_circ_256435,RMVar_hsa_circ_256436,RMVar_hsa_circ_61227,RMVar_hsa_circ_47856,RMVar_hsa_circ_368802,RMVar_hsa_circ_256450,RMVar_hsa_circ_125526,RMVar_hsa_circ_38224,RMVar_hsa_circ_256438,RMVar_hsa_circ_298663,RMVar_hsa_circ_302696,RMVar_hsa_circ_323255,RMVar_hsa_circ_300254,RMVar_hsa_circ_294493,RMVar_hsa_circ_270766,RMVar_hsa_circ_256445,RMVar_hsa_circ_256447,RMVar_hsa_circ_256448,RMVar_hsa_circ_256446,RMVar_hsa_circ_276368,RMVar_hsa_circ_334323,RMVar_hsa_circ_365844,RMVar_hsa_circ_286942,RMVar_hsa_circ_305118,RMVar_hsa_circ_284193,RMVar_hsa_circ_274043,RMVar_hsa_circ_271964,RMVar_hsa_circ_256454,RMVar_hsa_circ_256458,RMVar_hsa_circ_87464,RMVar_hsa_circ_256456,RMVar_hsa_circ_256457,RMVar_hsa_circ_256455,RMVar_hsa_circ_256452,RMVar_hsa_circ_256453,RMVar_hsa_circ_256451,RMVar_hsa_circ_256461,RMVar_hsa_circ_297740,RMVar_hsa_circ_362765,RMVar_hsa_circ_374877,RMVar_hsa_circ_256449,RMVar_hsa_circ_366282,RMVar_hsa_circ_310332,RMVar_hsa_circ_56216,RMVar_hsa_circ_275162,RMVar_hsa_circ_256462,RMVar_hsa_circ_256463,RMVar_hsa_circ_256464,RMVar_hsa_circ_256465 9961 RMVar_ID_9961 Human_SNP_ID_396895356 A-to-I Human chr9 - 33980823 33980823 33980823 CCCACCTCAGCGTCCCTAGTAGCTGGGACTACAGGTGCACGCTACTATGCCCAGCTAATTTTTGT CCCACCTCAGCGTCCCTAGTAGCTGGGACTACGGGTGCACGCTACTATGCCCAGCTAATTTTTGT T C UBAP2 Ensembl:ENSG00000137073 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs371616706 Functional Loss SNV dbSNP153 33..33 33 - - - 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_365844,RMVar_hsa_circ_286942,RMVar_hsa_circ_305118,RMVar_hsa_circ_274043,RMVar_hsa_circ_256454,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_56216,RMVar_hsa_circ_288718,RMVar_hsa_circ_256464,RMVar_hsa_circ_339296,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_352060,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_256476,RMVar_hsa_circ_323107 9962 RMVar_ID_9962 Human_SNP_ID_396897032 A-to-I Human chr9 - 33985839 33985839 33985839 TTTTGTATTTTTGCTAGACATGGGGTTTTACCATGTTGGCCAGGCTGGTCTCAAACTCCTGGCCT TTTTGTATTTTTGCTAGACATGGGGTTTTACCGTGTTGGCCAGGCTGGTCTCAAACTCCTGGCCT T C UBAP2 Ensembl:ENSG00000137073 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs961530222 Functional Loss SNV dbSNP153 33..33 33 - - - 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_365844,RMVar_hsa_circ_286942,RMVar_hsa_circ_305118,RMVar_hsa_circ_274043,RMVar_hsa_circ_256454,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_56216,RMVar_hsa_circ_288718,RMVar_hsa_circ_256464,RMVar_hsa_circ_339296,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_352060,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_256476,RMVar_hsa_circ_323107,RMVar_hsa_circ_256482 9963 RMVar_ID_9963 Human_SNP_ID_396897056 A-to-I Human chr9 - 33985937 33985933 33985937 AGCTAACTGCAACCTCCACCTCCTGGGCTCAAACAATCCTCCTACTTACCCTCCTGAGTAGCTGG AGCTAACTGCAACCTCCACCTCCTGGGCTCAA____TCCTCCTACTTACCCTCCTGAGTAGCTGG ATTGT A UBAP2 Ensembl:ENSG00000137073 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1292959736 Functional Loss DEL dbSNP153 33..36 33 - - - 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_365844,RMVar_hsa_circ_286942,RMVar_hsa_circ_305118,RMVar_hsa_circ_274043,RMVar_hsa_circ_256454,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_56216,RMVar_hsa_circ_288718,RMVar_hsa_circ_256464,RMVar_hsa_circ_339296,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_352060,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_256476,RMVar_hsa_circ_323107,RMVar_hsa_circ_256482 9964 RMVar_ID_9964 Human_SNP_ID_396897059 A-to-I Human chr9 - 33985937 33985937 33985937 AGCTAACTGCAACCTCCACCTCCTGGGCTCAAACAATCCTCCTACTTACCCTCCTGAGTAGCTGG AGCTAACTGCAACCTCCACCTCCTGGGCTCAAGCAATCCTCCTACTTACCCTCCTGAGTAGCTGG T C UBAP2 Ensembl:ENSG00000137073 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs949489211 Functional Loss SNV dbSNP153 33..33 33 - - - 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_365844,RMVar_hsa_circ_286942,RMVar_hsa_circ_305118,RMVar_hsa_circ_274043,RMVar_hsa_circ_256454,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_56216,RMVar_hsa_circ_288718,RMVar_hsa_circ_256464,RMVar_hsa_circ_339296,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_352060,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_256476,RMVar_hsa_circ_323107,RMVar_hsa_circ_256482 9965 RMVar_ID_9965 Human_SNP_ID_396897977 A-to-I Human chr9 - 33989291 33989288 33989291 AGACTGAGGCAGGAGAATGTTGTGAACCTGGGAGGCGGAGCTTGCAGTGAGCTGAGAGGGCGCCA AGACTGAGGCAGGAGAATGTTGTGAACCTGGG___CGGAGCTTGCAGTGAGCTGAGAGGGCGCCA GCCT G UBAP2 Ensembl:ENSG00000137073 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs988894113 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_16661335 RMVar_hsa_circ_121448,RMVar_hsa_circ_256408,RMVar_hsa_circ_110369,RMVar_hsa_circ_3151,RMVar_hsa_circ_256411,RMVar_hsa_circ_119005,RMVar_hsa_circ_126475,RMVar_hsa_circ_93999,RMVar_hsa_circ_256420,RMVar_hsa_circ_256421,RMVar_hsa_circ_256419,RMVar_hsa_circ_84253,RMVar_hsa_circ_256423,RMVar_hsa_circ_47856,RMVar_hsa_circ_256450,RMVar_hsa_circ_38224,RMVar_hsa_circ_298663,RMVar_hsa_circ_294493,RMVar_hsa_circ_256447,RMVar_hsa_circ_256448,RMVar_hsa_circ_334323,RMVar_hsa_circ_305118,RMVar_hsa_circ_274043,RMVar_hsa_circ_87464,RMVar_hsa_circ_256452,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_288718,RMVar_hsa_circ_256464,RMVar_hsa_circ_340458,RMVar_hsa_circ_283254,RMVar_hsa_circ_256470,RMVar_hsa_circ_256471,RMVar_hsa_circ_256469,RMVar_hsa_circ_256481,RMVar_hsa_circ_297548,RMVar_hsa_circ_350421,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_256482,RMVar_hsa_circ_372313,RMVar_hsa_circ_279801,RMVar_hsa_circ_256485,RMVar_hsa_circ_256483,RMVar_hsa_circ_292625,RMVar_hsa_circ_337365,RMVar_hsa_circ_256487 9966 RMVar_ID_9966 Human_SNP_ID_396898392 A-to-I Human chr9 - 33990814 33990814 33990814 TGGCCAACATGGTGAAACCCCGTCTCTACTAAAATTACAAAAATTCACTGGGTGTGGTGGTGTAC TGGCCAACATGGTGAAACCCCGTCTCTACTAAGATTACAAAAATTCACTGGGTGTGGTGGTGTAC T C UBAP2 Ensembl:ENSG00000137073 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs538266657 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121448,RMVar_hsa_circ_256408,RMVar_hsa_circ_110369,RMVar_hsa_circ_3151,RMVar_hsa_circ_256411,RMVar_hsa_circ_119005,RMVar_hsa_circ_126475,RMVar_hsa_circ_93999,RMVar_hsa_circ_256420,RMVar_hsa_circ_256421,RMVar_hsa_circ_256419,RMVar_hsa_circ_84253,RMVar_hsa_circ_256423,RMVar_hsa_circ_47856,RMVar_hsa_circ_256450,RMVar_hsa_circ_38224,RMVar_hsa_circ_298663,RMVar_hsa_circ_294493,RMVar_hsa_circ_256447,RMVar_hsa_circ_256448,RMVar_hsa_circ_334323,RMVar_hsa_circ_305118,RMVar_hsa_circ_274043,RMVar_hsa_circ_87464,RMVar_hsa_circ_256452,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_288718,RMVar_hsa_circ_256464,RMVar_hsa_circ_340458,RMVar_hsa_circ_283254,RMVar_hsa_circ_256470,RMVar_hsa_circ_256471,RMVar_hsa_circ_256469,RMVar_hsa_circ_256481,RMVar_hsa_circ_297548,RMVar_hsa_circ_350421,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_256482,RMVar_hsa_circ_372313,RMVar_hsa_circ_279801,RMVar_hsa_circ_256485,RMVar_hsa_circ_256483,RMVar_hsa_circ_292625,RMVar_hsa_circ_337365,RMVar_hsa_circ_256487 9967 RMVar_ID_9967 Human_SNP_ID_396899261 A-to-I Human chr9 - 33994032 33994032 33994032 AAATTAGCCAGGTGTGGTGGTGGGCGCCTGCAATCCCAGCTACTCAGGCGGCTGAGGCAGGAGAA AAATTAGCCAGGTGTGGTGGTGGGCGCCTGCAGTCCCAGCTACTCAGGCGGCTGAGGCAGGAGAA T C UBAP2 Ensembl:ENSG00000137073 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs184207515 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121448,RMVar_hsa_circ_256408,RMVar_hsa_circ_110369,RMVar_hsa_circ_3151,RMVar_hsa_circ_256411,RMVar_hsa_circ_119005,RMVar_hsa_circ_126475,RMVar_hsa_circ_93999,RMVar_hsa_circ_256420,RMVar_hsa_circ_256421,RMVar_hsa_circ_256419,RMVar_hsa_circ_84253,RMVar_hsa_circ_256423,RMVar_hsa_circ_47856,RMVar_hsa_circ_256450,RMVar_hsa_circ_38224,RMVar_hsa_circ_298663,RMVar_hsa_circ_294493,RMVar_hsa_circ_256447,RMVar_hsa_circ_256448,RMVar_hsa_circ_334323,RMVar_hsa_circ_305118,RMVar_hsa_circ_274043,RMVar_hsa_circ_87464,RMVar_hsa_circ_256452,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_288718,RMVar_hsa_circ_256464,RMVar_hsa_circ_340458,RMVar_hsa_circ_283254,RMVar_hsa_circ_256470,RMVar_hsa_circ_256471,RMVar_hsa_circ_256469,RMVar_hsa_circ_256481,RMVar_hsa_circ_297548,RMVar_hsa_circ_350421,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_256482,RMVar_hsa_circ_372313,RMVar_hsa_circ_279801,RMVar_hsa_circ_256485,RMVar_hsa_circ_256483,RMVar_hsa_circ_292625,RMVar_hsa_circ_337365,RMVar_hsa_circ_256487 9968 RMVar_ID_9968 Human_SNP_ID_396899568 A-to-I Human chr9 - 33995249 33995249 33995249 GGGTTCAAGTGATTCTTTTGCCTCAGCCTCCCAAGTAGCTAGTACTACAGGCATGCGCCACCACG GGGTTCAAGTGATTCTTTTGCCTCAGCCTCCCGAGTAGCTAGTACTACAGGCATGCGCCACCACG T C UBAP2 Ensembl:ENSG00000137073 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1400367711 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121448,RMVar_hsa_circ_256408,RMVar_hsa_circ_110369,RMVar_hsa_circ_3151,RMVar_hsa_circ_256411,RMVar_hsa_circ_119005,RMVar_hsa_circ_126475,RMVar_hsa_circ_93999,RMVar_hsa_circ_256420,RMVar_hsa_circ_256421,RMVar_hsa_circ_256419,RMVar_hsa_circ_84253,RMVar_hsa_circ_256423,RMVar_hsa_circ_47856,RMVar_hsa_circ_256450,RMVar_hsa_circ_38224,RMVar_hsa_circ_298663,RMVar_hsa_circ_294493,RMVar_hsa_circ_256447,RMVar_hsa_circ_256448,RMVar_hsa_circ_334323,RMVar_hsa_circ_305118,RMVar_hsa_circ_274043,RMVar_hsa_circ_87464,RMVar_hsa_circ_256452,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_288718,RMVar_hsa_circ_256464,RMVar_hsa_circ_340458,RMVar_hsa_circ_283254,RMVar_hsa_circ_256470,RMVar_hsa_circ_256471,RMVar_hsa_circ_256469,RMVar_hsa_circ_256481,RMVar_hsa_circ_297548,RMVar_hsa_circ_350421,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_256482,RMVar_hsa_circ_372313,RMVar_hsa_circ_279801,RMVar_hsa_circ_256485,RMVar_hsa_circ_256483,RMVar_hsa_circ_292625,RMVar_hsa_circ_337365,RMVar_hsa_circ_256487 9969 RMVar_ID_9969 Human_SNP_ID_396903195 A-to-I Human chr9 - 34008075 34008075 34008075 GCTGGAGTGCAGTGGCGCGATCTCGGCTCACTACAACCTTCGCCTCCCAGGTTCAAGCGATTCTC GCTGGAGTGCAGTGGCGCGATCTCGGCTCACTGCAACCTTCGCCTCCCAGGTTCAAGCGATTCTC T C UBAP2 Ensembl:ENSG00000137073 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1392760338 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16661902 RMVar_hsa_circ_256408,RMVar_hsa_circ_110369,RMVar_hsa_circ_119005,RMVar_hsa_circ_256421,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 9970 RMVar_ID_9970 Human_SNP_ID_396903680 A-to-I Human chr9 - 34009533 34009533 34009533 TTTTGAACCGGGACATGGTGGCTAACACCTGTAATCTCAACACTTTGGGAGGCTGAGGTGGGAGG TTTTGAACCGGGACATGGTGGCTAACACCTGTGATCTCAACACTTTGGGAGGCTGAGGTGGGAGG T C UBAP2 Ensembl:ENSG00000137073 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs914576128 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2890233 RMVar_hsa_circ_256408,RMVar_hsa_circ_110369,RMVar_hsa_circ_119005,RMVar_hsa_circ_256421,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 9971 RMVar_ID_9971 Human_SNP_ID_396905442 A-to-I Human chr9 - 34015958 34015958 34015958 ATAGACTTTAAAAAGCTGCCTTTGCTGGGCATAGTGGCTCATGTCTGTAATCTCAACACTTTGGG ATAGACTTTAAAAAGCTGCCTTTGCTGGGCATGGTGGCTCATGTCTGTAATCTCAACACTTTGGG T C UBAP2 Ensembl:ENSG00000137073 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs954350742 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16662044,Human_RBP_ID_26220982 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_256493,RMVar_hsa_circ_291348 9972 RMVar_ID_9972 Human_SNP_ID_396907487 A-to-I Human chr9 - 34021813 34021813 34021813 CCTGACCAACAAGTTGAGACCCCATCTCTACTAAAAATACAAAAATTAGTCGGGCGTGGTGGCAG CCTGACCAACAAGTTGAGACCCCATCTCTACTGAAAATACAAAAATTAGTCGGGCGTGGTGGCAG T C UBAP2 Ensembl:ENSG00000137073 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1280005231 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 9973 RMVar_ID_9973 Human_SNP_ID_396909640 A-to-I Human chr9 - 34029865 34029865 34029865 CTCTTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGTGCCCCCACCACAGCGGCCTAATTTTTG CTCTTGCCTCAGCCTCCCGAGTAGCTGGGATTGCAGGTGCCCCCACCACAGCGGCCTAATTTTTG T C UBAP2 Ensembl:ENSG00000137073 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1318844749 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 9974 RMVar_ID_9974 Human_SNP_ID_396909648 A-to-I Human chr9 - 34029901 34029901 34029901 CTCACTGCAACCTCTGCCTCTCGGGTTCAAGCAGTTCTCTTGCCTCAGCCTCCCGAGTAGCTGGG CTCACTGCAACCTCTGCCTCTCGGGTTCAAGCTGTTCTCTTGCCTCAGCCTCCCGAGTAGCTGGG T A UBAP2 Ensembl:ENSG00000137073 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1422049115 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16662417 RMVar_hsa_circ_87464,RMVar_hsa_circ_256449,RMVar_hsa_circ_256481,RMVar_hsa_circ_80358,RMVar_hsa_circ_121180,RMVar_hsa_circ_256490 9975 RMVar_ID_9975 Human_SNP_ID_396910262 A-to-I Human chr9 - 34031934 34031934 34031934 GGAGGTCTTGCTATGTTACCCAGGCTGGTCTCAAACTCCTGGGCTCAAGAAGTCCTCCCTCCTTG GGAGGTCTTGCTATGTTACCCAGGCTGGTCTCGAACTCCTGGGCTCAAGAAGTCCTCCCTCCTTG T C UBAP2 Ensembl:ENSG00000137073 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs573565200 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 9976 RMVar_ID_9976 Human_SNP_ID_396910488 A-to-I Human chr9 - 34032780 34032780 34032780 AGCTGAGATTACAGGTGCGTGCAACCACGCCCAGCTAATTTTTGTATTGTTTGTAAAGATAGGGT AGCTGAGATTACAGGTGCGTGCAACCACGCCCGGCTAATTTTTGTATTGTTTGTAAAGATAGGGT T C UBAP2 Ensembl:ENSG00000137073 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs945228682 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 9977 RMVar_ID_9977 Human_SNP_ID_396910493 A-to-I Human chr9 - 34032789 34032789 34032789 CTCTGGACTAGCTGAGATTACAGGTGCGTGCAACCACGCCCAGCTAATTTTTGTATTGTTTGTAA CTCTGGACTAGCTGAGATTACAGGTGCGTGCAGCCACGCCCAGCTAATTTTTGTATTGTTTGTAA T C UBAP2 Ensembl:ENSG00000137073 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs554599933 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 9978 RMVar_ID_9978 Human_SNP_ID_396913990 A-to-I Human chr9 - 34042889 34042889 34042889 TAATTTTTCTTTTTGTAGAGAGGAGTCTTGCTATGTTGCCCAGGCTGGTCTCTTAGGCTAAAGTG TAATTTTTCTTTTTGTAGAGAGGAGTCTTGCTGTGTTGCCCAGGCTGGTCTCTTAGGCTAAAGTG T C UBAP2 Ensembl:ENSG00000137073 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs148682128 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 9979 RMVar_ID_9979 Human_SNP_ID_396914568 A-to-I Human chr9 - 34044783 34044783 34044783 TCGCCCACTGCAACCTCTGCCCACCGGGTTCAAGTGATGCTCCTGCCTCAGCCTCCTGAGTAGCT TCGCCCACTGCAACCTCTGCCCACCGGGTTCACGTGATGCTCCTGCCTCAGCCTCCTGAGTAGCT T G UBAP2 Ensembl:ENSG00000137073 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054767372 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16662983 RMVar_hsa_circ_87464,RMVar_hsa_circ_256449,RMVar_hsa_circ_256481,RMVar_hsa_circ_80358,RMVar_hsa_circ_121180,RMVar_hsa_circ_256490 9980 RMVar_ID_9980 Human_SNP_ID_396914709 A-to-I Human chr9 - 34045224 34045224 34045224 TTCCTGCCTCAGCCTCCCGAGTACCTGGGACTACTGGCGCCTGCCGCCACGCCCGGCTAATTTTT TTCCTGCCTCAGCCTCCCGAGTACCTGGGACTGCTGGCGCCTGCCGCCACGCCCGGCTAATTTTT T C UBAP2 Ensembl:ENSG00000137073 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs562725841 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 9981 RMVar_ID_9981 Human_SNP_ID_396929750 A-to-I Human chr9 - 34101164 34101164 34101164 GGGAGGCTGGGGCAGGAGAATTGCTGAAGCCCAGGAGGTTGAGGCTACAATGAGCCATAATCATG GGGAGGCTGGGGCAGGAGAATTGCTGAAGCCCTGGAGGTTGAGGCTACAATGAGCCATAATCATG T A DCAF12 Ensembl:ENSG00000198876 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027583067 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26243122 RMVar_hsa_circ_22932,RMVar_hsa_circ_311483 9982 RMVar_ID_9982 Human_SNP_ID_396929751 A-to-I Human chr9 - 34101164 34101164 34101164 GGGAGGCTGGGGCAGGAGAATTGCTGAAGCCCAGGAGGTTGAGGCTACAATGAGCCATAATCATG GGGAGGCTGGGGCAGGAGAATTGCTGAAGCCCGGGAGGTTGAGGCTACAATGAGCCATAATCATG T C DCAF12 Ensembl:ENSG00000198876 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027583067 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26243122 RMVar_hsa_circ_22932,RMVar_hsa_circ_311483 9983 RMVar_ID_9983 Human_SNP_ID_396929768 A-to-I Human chr9 - 34101277 34101277 34101277 GGTCAGGAGTCCAAGACCAGCCTGGGTAACATAGTGAGACCCCATTTCTACAAAAAAATGAAAAT GGTCAGGAGTCCAAGACCAGCCTGGGTAACATGGTGAGACCCCATTTCTACAAAAAAATGAAAAT T C DCAF12 Ensembl:ENSG00000198876 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1245734582 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22932,RMVar_hsa_circ_311483 9984 RMVar_ID_9984 Human_SNP_ID_396930389 A-to-I Human chr9 - 34103688 34103687 34103689 ACCACACCCGGTTAATTATTTCTATTTTTTATAGAGACTGGGTCTCGCTTTGTTGCCCAGGCTGC ACCACACCCGGTTAATTATTTCTATTTTTTA__GAGACTGGGTCTCGCTTTGTTGCCCAGGCTGC CTA C DCAF12 Ensembl:ENSG00000198876 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs879782857 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_22932,RMVar_hsa_circ_311483 9985 RMVar_ID_9985 Human_SNP_ID_396930492 A-to-I Human chr9 - 34104086 34104086 34104086 TTTTGTATTTTTGGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTCCTGACTT TTTTGTATTTTTGGTAGAGACAGGGTTTCACCCTGTTGGCCAGGCTGGTCTCAAACTCCTGACTT T G DCAF12 Ensembl:ENSG00000198876 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1348028426 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22932,RMVar_hsa_circ_311483 9986 RMVar_ID_9986 Human_SNP_ID_396930965 A-to-I Human chr9 - 34105943 34105943 34105943 GAGTTCGAGACCAGGCTGGCCAGCATGGTGAAACCCTGTCTCTACTAAAAGTACAAAAAATTAGC GAGTTCGAGACCAGGCTGGCCAGCATGGTGAAGCCCTGTCTCTACTAAAAGTACAAAAAATTAGC T C DCAF12 Ensembl:ENSG00000198876 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1170026383 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22932,RMVar_hsa_circ_311483 9987 RMVar_ID_9987 Human_SNP_ID_396930980 A-to-I Human chr9 - 34106021 34106021 34106021 AATATAGGCCGGGTGTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGTGG AATATAGGCCGGGTGTGGTGGCTCACACCTGTGATCCCAGCACTTTGGGAGGCCGAGGTGGGTGG T C DCAF12 Ensembl:ENSG00000198876 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1277979686 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22932,RMVar_hsa_circ_311483 9988 RMVar_ID_9988 Human_SNP_ID_396934196 A-to-I Human chr9 - 34118316 34118316 34118316 CAGCCCGGCCAACATGATGAAATCCCGTCTCTACTAAAAACACAAAAATTAGCCGGGCATGATGC CAGCCCGGCCAACATGATGAAATCCCGTCTCTGCTAAAAACACAAAAATTAGCCGGGCATGATGC T C DCAF12 Ensembl:ENSG00000198876 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1477648596 Functional Loss SNV dbSNP153 33..33 33 - - - 9989 RMVar_ID_9989 Human_SNP_ID_396934304 A-to-I Human chr9 - 34118779 34118779 34118779 TTGTATTTTTAGTAGAGATGGGGTCTTGCCATATTGGCCAGCCTGGTTTTGAACTCCTGACCTCA TTGTATTTTTAGTAGAGATGGGGTCTTGCCATGTTGGCCAGCCTGGTTTTGAACTCCTGACCTCA T C DCAF12 Ensembl:ENSG00000198876 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1018406812 Functional Loss SNV dbSNP153 33..33 33 - - - 9990 RMVar_ID_9990 Human_SNP_ID_396934570 A-to-I Human chr9 - 34119884 34119884 34119884 CAGCCTGGGCAATGTAGTGAGACCCCATCTCTACAAAATATTTAAGAATTAGCTGGGCATGGTGG CAGCCTGGGCAATGTAGTGAGACCCCATCTCTGCAAAATATTTAAGAATTAGCTGGGCATGGTGG T C DCAF12 Ensembl:ENSG00000198876 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1190060154 Functional Loss SNV dbSNP153 33..33 33 - - - 9991 RMVar_ID_9991 Human_SNP_ID_396952082 A-to-I Human chr9 + 34183970 34183970 34183970 TTTTGTGTTTTTAGTAGAGACGGGGTTTCTCCATGTTGGTCAGGCTGGTCTCAAACTCTTCAACT TTTTGTGTTTTTAGTAGAGACGGGGTTTCTCCGTGTTGGTCAGGCTGGTCTCAAACTCTTCAACT A G UBAP1 Ensembl:ENSG00000165006 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1245504245 Functional Loss SNV dbSNP153 33..33 33 - - - 9992 RMVar_ID_9992 Human_SNP_ID_396953458 A-to-I Human chr9 + 34188907 34188907 34188907 TGAAGCCGGGAGGCAGAGGTTTCGGTGAGCCGAGATCGTACCATTGCACTCCAGCCTGGCCGACA TGAAGCCGGGAGGCAGAGGTTTCGGTGAGCCGGGATCGTACCATTGCACTCCAGCCTGGCCGACA A G UBAP1 Ensembl:ENSG00000165006 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042401861 Functional Loss SNV dbSNP153 33..33 33 - - - 9993 RMVar_ID_9993 Human_SNP_ID_396954120 A-to-I Human chr9 + 34191335 34191335 34191335 TGTTCCCTGGTCTGAAACTTCTGGCCTCAAGCAGTCTTCCCACCTTGGCCTCCTAAAGCACCAGG TGTTCCCTGGTCTGAAACTTCTGGCCTCAAGCGGTCTTCCCACCTTGGCCTCCTAAAGCACCAGG A G UBAP1 Ensembl:ENSG00000165006 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1222812855 Functional Loss SNV dbSNP153 33..33 33 - - - 9994 RMVar_ID_9994 Human_SNP_ID_396954902 A-to-I Human chr9 + 34194408 34194408 34194408 ACAATCTCGGCTCGCTGTAAACTCCGCCTCCCAGGTTCACGCCATTCTCCTGCCTCAGCCTCCTC ACAATCTCGGCTCGCTGTAAACTCCGCCTCCCGGGTTCACGCCATTCTCCTGCCTCAGCCTCCTC A G UBAP1 Ensembl:ENSG00000165006 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1380241490 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16663905 9995 RMVar_ID_9995 Human_SNP_ID_396961407 A-to-I Human chr9 + 34219201 34219201 34219201 GCCTTGACTTCCTGGGCTCAGGTGATTCTCCTACCTCAGCCTCCCGAGTAGCAGGGACTACAGGC GCCTTGACTTCCTGGGCTCAGGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCAGGGACTACAGGC A G UBAP1 Ensembl:ENSG00000165006 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1184548212 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_256497,RMVar_hsa_circ_348137 9996 RMVar_ID_9996 Human_SNP_ID_396961416 A-to-I Human chr9 + 34219234 34219234 34219234 CCTCAGCCTCCCGAGTAGCAGGGACTACAGGCATGCAACACCACACCGGCAAATTTTTTGTATCT CCTCAGCCTCCCGAGTAGCAGGGACTACAGGCTTGCAACACCACACCGGCAAATTTTTTGTATCT A T UBAP1 Ensembl:ENSG00000165006 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1254796013 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_256497,RMVar_hsa_circ_348137 9997 RMVar_ID_9997 Human_SNP_ID_396961418 A-to-I Human chr9 + 34219238 34219238 34219238 AGCCTCCCGAGTAGCAGGGACTACAGGCATGCAACACCACACCGGCAAATTTTTTGTATCTTTGT AGCCTCCCGAGTAGCAGGGACTACAGGCATGCTACACCACACCGGCAAATTTTTTGTATCTTTGT A T UBAP1 Ensembl:ENSG00000165006 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1327400348 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_256497,RMVar_hsa_circ_348137 9998 RMVar_ID_9998 Human_SNP_ID_396962906 A-to-I Human chr9 + 34223309 34223309 34223309 AAAATTAGCCGGGTGTAGTGACGCATGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGAAGGAGA AAAATTAGCCGGGTGTAGTGACGCATGCCTGTGATCCCAGCTACTCGGGAGGCTGAGGAAGGAGA A G UBAP1 Ensembl:ENSG00000165006 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1182553081 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_256498,RMVar_hsa_circ_298733,RMVar_hsa_circ_348137,RMVar_hsa_circ_354563,RMVar_hsa_circ_256499 9999 RMVar_ID_9999 Human_SNP_ID_396968578 A-to-I Human chr9 + 34246300 34246300 34246300 GTTGTCCAGGCTGGTCTCAAAATTCTGAGCTTAAGCAGTCCTTCTGCCTCAGCCTCCCAAAGTGC GTTGTCCAGGCTGGTCTCAAAATTCTGAGCTTGAGCAGTCCTTCTGCCTCAGCCTCCCAAAGTGC A G UBAP1 Ensembl:ENSG00000165006 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1257340107 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119697,RMVar_hsa_circ_256502 10000 RMVar_ID_10000 Human_SNP_ID_396992410 A-to-I Human chr9 + 34339571 34339571 34339571 TTGACTAGAAAATCCTGTTTTCAGCCAGGCACAGTGGCACACGCCTATAATCCCAGCACTTTTGG TTGACTAGAAAATCCTGTTTTCAGCCAGGCACGGTGGCACACGCCTATAATCCCAGCACTTTTGG A G NUDT2 Ensembl:ENSG00000164978 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1180427468 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75884,RMVar_hsa_circ_256517 10001 RMVar_ID_10001 Human_SNP_ID_396992416 A-to-I Human chr9 + 34339585 34339585 34339585 CTGTTTTCAGCCAGGCACAGTGGCACACGCCTATAATCCCAGCACTTTTGGAGGTCGAGGTGGGC CTGTTTTCAGCCAGGCACAGTGGCACACGCCTGTAATCCCAGCACTTTTGGAGGTCGAGGTGGGC A G NUDT2 Ensembl:ENSG00000164978 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs559841129 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75884,RMVar_hsa_circ_256517 10002 RMVar_ID_10002 Human_SNP_ID_397011297 A-to-I Human chr9 - 34416942 34416942 34416942 GTACCTGTAATCCCAGATACACGGGAAGCTGAAGTAGTAGGATCACTTGAGTCCAGGAGTTCAAG GTACCTGTAATCCCAGATACACGGGAAGCTGAGGTAGTAGGATCACTTGAGTCCAGGAGTTCAAG T C FAM219A Ensembl:ENSG00000164970 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1001432622 Functional Loss SNV dbSNP153 33..33 33 - - - 10003 RMVar_ID_10003 Human_SNP_ID_397064461 A-to-I Human chr9 - 34637091 34637091 34637091 TACCCTGATAGTGTCATGTGCGATTGTCACTCAGGGCGCTACTGGGCTGAGATCTCGGATACCAT TACCCTGATAGTGTCATGTGCGATTGTCACTCTGGGCGCTACTGGGCTGAGATCTCGGATACCAT T A SIGMAR1 Ensembl:ENSG00000147955 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11559050 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_963105,Human_RBP_ID_1227243,Human_RBP_ID_3212353,Human_RBP_ID_16666382,Human_RBP_ID_17666284,Human_RBP_ID_19144840,Human_RBP_ID_24300966 Human_Splice_Rec_1039817,Human_Splice_Rec_1039823,Human_Splice_Rec_1039829,Human_Splice_Rec_1039839 RMVar_hsa_circ_108807,RMVar_hsa_circ_35055,RMVar_hsa_circ_256531 10004 RMVar_ID_10004 Human_SNP_ID_397064462 A-to-I Human chr9 - 34637091 34637091 34637091 TACCCTGATAGTGTCATGTGCGATTGTCACTCAGGGCGCTACTGGGCTGAGATCTCGGATACCAT TACCCTGATAGTGTCATGTGCGATTGTCACTCGGGGCGCTACTGGGCTGAGATCTCGGATACCAT T C SIGMAR1 Ensembl:ENSG00000147955 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11559050 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_963105,Human_RBP_ID_1227243,Human_RBP_ID_3212353,Human_RBP_ID_16666382,Human_RBP_ID_17666284,Human_RBP_ID_19144840,Human_RBP_ID_24300966 Human_Splice_Rec_1039817,Human_Splice_Rec_1039823,Human_Splice_Rec_1039829,Human_Splice_Rec_1039839 RMVar_hsa_circ_108807,RMVar_hsa_circ_35055,RMVar_hsa_circ_256531 10005 RMVar_ID_10005 Human_SNP_ID_397064463 A-to-I Human chr9 - 34637091 34637091 34637091 TACCCTGATAGTGTCATGTGCGATTGTCACTCAGGGCGCTACTGGGCTGAGATCTCGGATACCAT TACCCTGATAGTGTCATGTGCGATTGTCACTCCGGGCGCTACTGGGCTGAGATCTCGGATACCAT T G SIGMAR1 Ensembl:ENSG00000147955 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11559050 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_963105,Human_RBP_ID_1227243,Human_RBP_ID_3212353,Human_RBP_ID_16666382,Human_RBP_ID_17666284,Human_RBP_ID_19144840,Human_RBP_ID_24300966 Human_Splice_Rec_1039817,Human_Splice_Rec_1039823,Human_Splice_Rec_1039829,Human_Splice_Rec_1039839 RMVar_hsa_circ_108807,RMVar_hsa_circ_35055,RMVar_hsa_circ_256531 10006 RMVar_ID_10006 Human_SNP_ID_397074884 A-to-I Human chr9 + 34676403 34676403 34676403 AAACTTTGCTGGGCATGGTGGCGGGCCCCTGTAGTCCCAGCTTCTCAGGAGGCTGAGGTGGAGGA AAACTTTGCTGGGCATGGTGGCGGGCCCCTGTTGTCCCAGCTTCTCAGGAGGCTGAGGTGGAGGA A T AL162231.2 Ensembl:ENSG00000230074 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1349514575 Functional Loss SNV dbSNP153 33..33 33 - - - 10007 RMVar_ID_10007 Human_SNP_ID_397076422 A-to-I Human chr9 + 34682054 34682054 34682054 TGGAGTGCAGTGTCATGGTCACGGCTCACTGCAGTCTCAACCTCCCAGGCTCGAGAGTTCCTCCC TGGAGTGCAGTGTCATGGTCACGGCTCACTGCGGTCTCAACCTCCCAGGCTCGAGAGTTCCTCCC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs974648086 Functional Loss SNV dbSNP153 33..33 33 - - - 10008 RMVar_ID_10008 Human_SNP_ID_397076475 A-to-I Human chr9 + 34682200 34682200 34682200 TTTTTTGTGGAGACATTGCCCAGACTGGTCTCAAATTCCTGGGCTGAAATGATCCTCCTGCTTTG TTTTTTGTGGAGACATTGCCCAGACTGGTCTCCAATTCCTGGGCTGAAATGATCCTCCTGCTTTG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1426787680 Functional Loss SNV dbSNP153 33..33 33 - - - 10009 RMVar_ID_10009 Human_SNP_ID_397162447 A-to-I Human chr9 - 35049995 35049995 35049995 TTGGTTGAGCGTGGTGATGGTGGCTCATGCCTATAATCCCAGCACTTTGAGAGGTCGAGACAGGA TTGGTTGAGCGTGGTGATGGTGGCTCATGCCTGTAATCCCAGCACTTTGAGAGGTCGAGACAGGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs759925418 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26221708 10010 RMVar_ID_10010 Human_SNP_ID_397172064 A-to-I Human chr9 - 35082219 35082219 35082219 TCGCTGTGTCACCTAGGCTAGAGTTCAGTGGCAGGATCTCGGCTCACTGCAACCTCCACCTTCCG TCGCTGTGTCACCTAGGCTAGAGTTCAGTGGCTGGATCTCGGCTCACTGCAACCTCCACCTTCCG T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1288438829 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16667805 10011 RMVar_ID_10011 Human_SNP_ID_397173208 A-to-I Human chr9 - 35086655 35086655 35086655 AAAATTAGCCAGGCATGGTCCCAGCTATGTAGAGGCTGAGGTGGATCACTTGAGCCCAGGAGTTA AAAATTAGCCAGGCATGGTCCCAGCTATGTAGTGGCTGAGGTGGATCACTTGAGCCCAGGAGTTA T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1384099285 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_718329,Human_RBP_ID_16667919 10012 RMVar_ID_10012 Human_SNP_ID_397173213 A-to-I Human chr9 - 35086681 35086681 35086681 CAAGACTCCGTCTCTACAAAAATAAAAAAATTAGCCAGGCATGGTCCCAGCTATGTAGAGGCTGA CAAGACTCCGTCTCTACAAAAATAAAAAAATTGGCCAGGCATGGTCCCAGCTATGTAGAGGCTGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs977281680 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_718329 10013 RMVar_ID_10013 Human_SNP_ID_397173215 A-to-I Human chr9 - 35086692 35086691 35086692 CTTGAGGATAGCAAGACTCCGTCTCTACAAAAATAAAAAAATTAGCCAGGCATGGTCCCAGCTAT CTTGAGGATAGCAAGACTCCGTCTCTACAAAA_TAAAAAAATTAGCCAGGCATGGTCCCAGCTAT AT A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1475403470 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_26221880 10014 RMVar_ID_10014 Human_SNP_ID_397173216 A-to-I Human chr9 - 35086695 35086695 35086695 TCACTTGAGGATAGCAAGACTCCGTCTCTACAAAAATAAAAAAATTAGCCAGGCATGGTCCCAGC TCACTTGAGGATAGCAAGACTCCGTCTCTACAGAAATAAAAAAATTAGCCAGGCATGGTCCCAGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1200210129 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26221880 10015 RMVar_ID_10015 Human_SNP_ID_397173232 A-to-I Human chr9 - 35086761 35086761 35086761 ATTTCTAGCCAGGCACTGTGGCATGTCCCTATAGTCCCAGCTACTTGGGAGGCAGAGGTGGGAGG ATTTCTAGCCAGGCACTGTGGCATGTCCCTATGGTCCCAGCTACTTGGGAGGCAGAGGTGGGAGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886622429 Functional Loss SNV dbSNP153 33..33 33 - - - 10016 RMVar_ID_10016 Human_SNP_ID_397173233 A-to-I Human chr9 - 35086763 35086763 35086763 TTATTTCTAGCCAGGCACTGTGGCATGTCCCTATAGTCCCAGCTACTTGGGAGGCAGAGGTGGGA TTATTTCTAGCCAGGCACTGTGGCATGTCCCTGTAGTCCCAGCTACTTGGGAGGCAGAGGTGGGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006309145 Functional Loss SNV dbSNP153 33..33 33 - - - 10017 RMVar_ID_10017 Human_SNP_ID_397173455 A-to-I Human chr9 - 35087681 35087678 35087682 TGCCTGGCTAATTTTTAAATTTCTGTACAGACAGAGTCTTGCTACATTGCCCAGGCTGTTCGTGA TGCCTGGCTAATTTTTAAATTTCTGTACAGA____GTCTTGCTACATTGCCCAGGCTGTTCGTGA CTCTG C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs548992379 Functional Loss DEL dbSNP153 32..35 33 - - - 10018 RMVar_ID_10018 Human_SNP_ID_397173462 A-to-I Human chr9 - 35087696 35087696 35087696 CAGTATCTGGGACCATGCCTGGCTAATTTTTAAATTTCTGTACAGACAGAGTCTTGCTACATTGC CAGTATCTGGGACCATGCCTGGCTAATTTTTACATTTCTGTACAGACAGAGTCTTGCTACATTGC T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs983164145 Functional Loss SNV dbSNP153 33..33 33 - - - 10019 RMVar_ID_10019 Human_SNP_ID_397173687 A-to-I Human chr9 - 35088748 35088748 35088748 TTGGTCCCAGGAGTTCAAGACCAGCCTGTGGAACATAACAAGACCCCGTCTCTACTATTTAAAAA TTGGTCCCAGGAGTTCAAGACCAGCCTGTGGAGCATAACAAGACCCCGTCTCTACTATTTAAAAA T C PIGO Ensembl:ENSG00000165282 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006958875 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_718340,Human_RBP_ID_8704134,Human_RBP_ID_16667999,Human_RBP_ID_26563596 10020 RMVar_ID_10020 Human_SNP_ID_397173707 A-to-I Human chr9 - 35088820 35088820 35088820 ATAAAATAGGCCGGGCGTGGTGACTTGCACCTATAATCCCAGCACTTTGGGAGGCAGAGGTGGGA ATAAAATAGGCCGGGCGTGGTGACTTGCACCTGTAATCCCAGCACTTTGGGAGGCAGAGGTGGGA T C PIGO Ensembl:ENSG00000165282 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1447429820 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_718342,Human_RBP_ID_23092404,Human_RBP_ID_26221891 Human_miRNA_ID_1361003 10021 RMVar_ID_10021 Human_SNP_ID_397177598 A-to-I Human chr9 - 35101562 35101562 35101562 GTTGAGGCTGTGGGGCTTACACCTCTTTTTCCAGGAACGGGAGTCCCTGAATGCCAGCATTGTGG GTTGAGGCTGTGGGGCTTACACCTCTTTTTCCGGGAACGGGAGTCCCTGAATGCCAGCATTGTGG T C STOML2 Ensembl:ENSG00000165283 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs769837253 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_961351 RMVar_hsa_circ_75983,RMVar_hsa_circ_118449,RMVar_hsa_circ_111866,RMVar_hsa_circ_86444,RMVar_hsa_circ_256563,RMVar_hsa_circ_256565,RMVar_hsa_circ_256564,RMVar_hsa_circ_256562 10022 RMVar_ID_10022 Human_SNP_ID_397266896 A-to-I Human chr9 + 35493597 35493592 35493597 ACGATCTTGGCTCACTGCAACTTTTGCCTCCCAGTTCAGGTGATTCACATGCCTCAGCCTCCTGA ACGATCTTGGCTCACTGCAACTTTTGCC_____GTTCAGGTGATTCACATGCCTCAGCCTCCTGA CTCCCA C RUSC2 Ensembl:ENSG00000198853 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749761602 Functional Loss DEL dbSNP153 29..33 33 - - - Human_RBP_ID_16668834 RMVar_hsa_circ_108460,RMVar_hsa_circ_256601 10023 RMVar_ID_10023 Human_SNP_ID_397271382 A-to-I Human chr9 + 35513382 35513382 35513382 CTCATGCCTCAGCCTCCCGAGCAGCTGGGATTACAGACACGTGCCACCATGCCAAGCTAATTTTC CTCATGCCTCAGCCTCCCGAGCAGCTGGGATTGCAGACACGTGCCACCATGCCAAGCTAATTTTC A G RUSC2 Ensembl:ENSG00000198853 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1329236073 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108460,RMVar_hsa_circ_256601 10024 RMVar_ID_10024 Human_SNP_ID_397275054 A-to-I Human chr9 + 35530152 35530152 35530152 TTTTGTATTTTTTGTAGAGACGGGGTTTCACCATGTTGCCGAGGCTGGTATCAACTCATAAGCTC TTTTGTATTTTTTGTAGAGACGGGGTTTCACCGTGTTGCCGAGGCTGGTATCAACTCATAAGCTC A G RUSC2 Ensembl:ENSG00000198853 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1253805336 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108460,RMVar_hsa_circ_256601 10025 RMVar_ID_10025 Human_SNP_ID_397275148 A-to-I Human chr9 + 35530656 35530656 35530656 GGTTTTTTGGTTGTTTTTTGTTTCTGTTTTTTATGAGACTGGGTCTCACTCTGTCGCCCAGGCTG GGTTTTTTGGTTGTTTTTTGTTTCTGTTTTTTTTGAGACTGGGTCTCACTCTGTCGCCCAGGCTG A T RUSC2 Ensembl:ENSG00000198853 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs912046415 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108460,RMVar_hsa_circ_256601 10026 RMVar_ID_10026 Human_SNP_ID_397307588 A-to-I Human chr9 - 35657898 35657894 35657898 GCAGAGAGTGCCACGTGCATACGCACGTAGACATTCCCCGCTTCCCACTCCAAAGTCCGCCAAGA GCAGAGAGTGCCACGTGCATACGCACGTAGAC____CCCGCTTCCCACTCCAAAGTCCGCCAAGA GGAAT G RMRP,RMRP:2 Ensembl:ENSG00000269900,Ensembl:ENSG00000277027 lincRNA,Other exon,exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1191061440 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_271138,Human_RBP_ID_287123,Human_RBP_ID_718454,Human_RBP_ID_1227307,Human_RBP_ID_1247876,Human_RBP_ID_1339058,Human_RBP_ID_1705182,Human_RBP_ID_2064328,Human_RBP_ID_3213003,Human_RBP_ID_3899791,Human_RBP_ID_5027731,Human_RBP_ID_5107165,Human_RBP_ID_5226365,Human_RBP_ID_5271402,Human_RBP_ID_5309961,Human_RBP_ID_5431202,Human_RBP_ID_5454509,Human_RBP_ID_5516141,Human_RBP_ID_5536152,Human_RBP_ID_5634107,Human_RBP_ID_7924753,Human_RBP_ID_8158314,Human_RBP_ID_8275239,Human_RBP_ID_8704239,Human_RBP_ID_8928297,Human_RBP_ID_9236322,Human_RBP_ID_10429842,Human_RBP_ID_16668969,Human_RBP_ID_17065642,Human_RBP_ID_17549653,Human_RBP_ID_17716558,Human_RBP_ID_18135621,Human_RBP_ID_18203403,Human_RBP_ID_18212273,Human_RBP_ID_18453544,Human_RBP_ID_18521201,Human_RBP_ID_18542012,Human_RBP_ID_18908532,Human_RBP_ID_21659701,Human_RBP_ID_22340121,Human_RBP_ID_22518311,Human_RBP_ID_22838649,Human_RBP_ID_23141632,Human_RBP_ID_23201297,Human_RBP_ID_23316704,Human_RBP_ID_24301863,Human_RBP_ID_24442804,Human_RBP_ID_26563624,Human_RBP_ID_26738291,Human_RBP_ID_26752287,Human_RBP_ID_27136347,Human_RBP_ID_27162477,Human_RBP_ID_27375103,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 10027 RMVar_ID_10027 Human_SNP_ID_397307597 A-to-I Human chr9 - 35657898 35657898 35657898 GCAGAGAGTGCCACGTGCATACGCACGTAGACATTCCCCGCTTCCCACTCCAAAGTCCGCCAAGA GCAGAGAGTGCCACGTGCATACGCACGTAGACTTTCCCCGCTTCCCACTCCAAAGTCCGCCAAGA T A RMRP,RMRP:2 Ensembl:ENSG00000269900,Ensembl:ENSG00000277027 lincRNA,Other exon,exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs557578605 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_271138,Human_RBP_ID_287123,Human_RBP_ID_718454,Human_RBP_ID_1227307,Human_RBP_ID_1247876,Human_RBP_ID_1339058,Human_RBP_ID_1705182,Human_RBP_ID_2064328,Human_RBP_ID_3213003,Human_RBP_ID_3899791,Human_RBP_ID_5027731,Human_RBP_ID_5107165,Human_RBP_ID_5226365,Human_RBP_ID_5271402,Human_RBP_ID_5309961,Human_RBP_ID_5431202,Human_RBP_ID_5454509,Human_RBP_ID_5516141,Human_RBP_ID_5536152,Human_RBP_ID_5634107,Human_RBP_ID_7924753,Human_RBP_ID_8158314,Human_RBP_ID_8275239,Human_RBP_ID_8704239,Human_RBP_ID_8928297,Human_RBP_ID_9236322,Human_RBP_ID_10429842,Human_RBP_ID_16668969,Human_RBP_ID_17065642,Human_RBP_ID_17549653,Human_RBP_ID_17716558,Human_RBP_ID_18135621,Human_RBP_ID_18203403,Human_RBP_ID_18212273,Human_RBP_ID_18453544,Human_RBP_ID_18521201,Human_RBP_ID_18542012,Human_RBP_ID_18908532,Human_RBP_ID_21659701,Human_RBP_ID_22340121,Human_RBP_ID_22518311,Human_RBP_ID_22838649,Human_RBP_ID_23141632,Human_RBP_ID_23201297,Human_RBP_ID_23316704,Human_RBP_ID_24301863,Human_RBP_ID_24442804,Human_RBP_ID_26563624,Human_RBP_ID_26738291,Human_RBP_ID_26752287,Human_RBP_ID_27136347,Human_RBP_ID_27162477,Human_RBP_ID_27375103,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 10028 RMVar_ID_10028 Human_SNP_ID_397307598 A-to-I Human chr9 - 35657898 35657898 35657898 GCAGAGAGTGCCACGTGCATACGCACGTAGACATTCCCCGCTTCCCACTCCAAAGTCCGCCAAGA GCAGAGAGTGCCACGTGCATACGCACGTAGACGTTCCCCGCTTCCCACTCCAAAGTCCGCCAAGA T C RMRP,RMRP:2 Ensembl:ENSG00000269900,Ensembl:ENSG00000277027 lincRNA,Other exon,exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs557578605 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_271138,Human_RBP_ID_287123,Human_RBP_ID_718454,Human_RBP_ID_1227307,Human_RBP_ID_1247876,Human_RBP_ID_1339058,Human_RBP_ID_1705182,Human_RBP_ID_2064328,Human_RBP_ID_3213003,Human_RBP_ID_3899791,Human_RBP_ID_5027731,Human_RBP_ID_5107165,Human_RBP_ID_5226365,Human_RBP_ID_5271402,Human_RBP_ID_5309961,Human_RBP_ID_5431202,Human_RBP_ID_5454509,Human_RBP_ID_5516141,Human_RBP_ID_5536152,Human_RBP_ID_5634107,Human_RBP_ID_7924753,Human_RBP_ID_8158314,Human_RBP_ID_8275239,Human_RBP_ID_8704239,Human_RBP_ID_8928297,Human_RBP_ID_9236322,Human_RBP_ID_10429842,Human_RBP_ID_16668969,Human_RBP_ID_17065642,Human_RBP_ID_17549653,Human_RBP_ID_17716558,Human_RBP_ID_18135621,Human_RBP_ID_18203403,Human_RBP_ID_18212273,Human_RBP_ID_18453544,Human_RBP_ID_18521201,Human_RBP_ID_18542012,Human_RBP_ID_18908532,Human_RBP_ID_21659701,Human_RBP_ID_22340121,Human_RBP_ID_22518311,Human_RBP_ID_22838649,Human_RBP_ID_23141632,Human_RBP_ID_23201297,Human_RBP_ID_23316704,Human_RBP_ID_24301863,Human_RBP_ID_24442804,Human_RBP_ID_26563624,Human_RBP_ID_26738291,Human_RBP_ID_26752287,Human_RBP_ID_27136347,Human_RBP_ID_27162477,Human_RBP_ID_27375103,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 10029 RMVar_ID_10029 Human_SNP_ID_397307599 A-to-I Human chr9 - 35657898 35657898 35657898 GCAGAGAGTGCCACGTGCATACGCACGTAGACATTCCCCGCTTCCCACTCCAAAGTCCGCCAAGA GCAGAGAGTGCCACGTGCATACGCACGTAGACCTTCCCCGCTTCCCACTCCAAAGTCCGCCAAGA T G RMRP,RMRP:2 Ensembl:ENSG00000269900,Ensembl:ENSG00000277027 lincRNA,Other exon,exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs557578605 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_271138,Human_RBP_ID_287123,Human_RBP_ID_718454,Human_RBP_ID_1227307,Human_RBP_ID_1247876,Human_RBP_ID_1339058,Human_RBP_ID_1705182,Human_RBP_ID_2064328,Human_RBP_ID_3213003,Human_RBP_ID_3899791,Human_RBP_ID_5027731,Human_RBP_ID_5107165,Human_RBP_ID_5226365,Human_RBP_ID_5271402,Human_RBP_ID_5309961,Human_RBP_ID_5431202,Human_RBP_ID_5454509,Human_RBP_ID_5516141,Human_RBP_ID_5536152,Human_RBP_ID_5634107,Human_RBP_ID_7924753,Human_RBP_ID_8158314,Human_RBP_ID_8275239,Human_RBP_ID_8704239,Human_RBP_ID_8928297,Human_RBP_ID_9236322,Human_RBP_ID_10429842,Human_RBP_ID_16668969,Human_RBP_ID_17065642,Human_RBP_ID_17549653,Human_RBP_ID_17716558,Human_RBP_ID_18135621,Human_RBP_ID_18203403,Human_RBP_ID_18212273,Human_RBP_ID_18453544,Human_RBP_ID_18521201,Human_RBP_ID_18542012,Human_RBP_ID_18908532,Human_RBP_ID_21659701,Human_RBP_ID_22340121,Human_RBP_ID_22518311,Human_RBP_ID_22838649,Human_RBP_ID_23141632,Human_RBP_ID_23201297,Human_RBP_ID_23316704,Human_RBP_ID_24301863,Human_RBP_ID_24442804,Human_RBP_ID_26563624,Human_RBP_ID_26738291,Human_RBP_ID_26752287,Human_RBP_ID_27136347,Human_RBP_ID_27162477,Human_RBP_ID_27375103,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 10030 RMVar_ID_10030 Human_SNP_ID_397318975 A-to-I Human chr9 - 35695719 35695719 35695719 GGGATGGTGGTGCACACCTGTAATTCCCAGCTACTTGGGAGGCTGAGGCACCAGAATTGCTTGAA GGGATGGTGGTGCACACCTGTAATTCCCAGCTGCTTGGGAGGCTGAGGCACCAGAATTGCTTGAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1020265755 Functional Loss SNV dbSNP153 33..33 33 - - - 10031 RMVar_ID_10031 Human_SNP_ID_397319784 A-to-I Human chr9 - 35698804 35698804 35698804 CCCAGAGAGAACTAGTGGCCCAAGGGAAGGTGAGTGCTTAAATACCCAGAAGAATGGGGACAGGT CCCAGAGAGAACTAGTGGCCCAAGGGAAGGTGGGTGCTTAAATACCCAGAAGAATGGGGACAGGT T C TLN1 Ensembl:ENSG00000137076 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1479936237 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5634116 RMVar_hsa_circ_76291,RMVar_hsa_circ_89989,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_97060,RMVar_hsa_circ_92285,RMVar_hsa_circ_256636,RMVar_hsa_circ_256644,RMVar_hsa_circ_83289,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_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,RMVar_hsa_circ_86505,RMVar_hsa_circ_94059,RMVar_hsa_circ_98509,RMVar_hsa_circ_256653,RMVar_hsa_circ_256654,RMVar_hsa_circ_266335,RMVar_hsa_circ_114930,RMVar_hsa_circ_256656,RMVar_hsa_circ_104156,RMVar_hsa_circ_256657,RMVar_hsa_circ_256658,RMVar_hsa_circ_256659 10032 RMVar_ID_10032 Human_SNP_ID_397319979 A-to-I Human chr9 - 35699420 35699420 35699420 AAGCCAAGCCCAGAACTGAAGCAGCAGTTGACAGGACATTCAAAGCGTGTGGCTGGTTCCGTCAC AAGCCAAGCCCAGAACTGAAGCAGCAGTTGACGGGACATTCAAAGCGTGTGGCTGGTTCCGTCAC T C TLN1 Ensembl:ENSG00000137076 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs759561962 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5637129,Human_RBP_ID_8928320,Human_RBP_ID_24301901 Human_Splice_Rec_1042456,Human_Splice_Rec_1042457 RMVar_hsa_circ_76291,RMVar_hsa_circ_89989,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_97060,RMVar_hsa_circ_92285,RMVar_hsa_circ_256636,RMVar_hsa_circ_256644,RMVar_hsa_circ_83289,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_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,RMVar_hsa_circ_86505,RMVar_hsa_circ_66996,RMVar_hsa_circ_94059,RMVar_hsa_circ_98509,RMVar_hsa_circ_256653,RMVar_hsa_circ_256654,RMVar_hsa_circ_114930,RMVar_hsa_circ_256656,RMVar_hsa_circ_104156,RMVar_hsa_circ_83504,RMVar_hsa_circ_256657,RMVar_hsa_circ_256658,RMVar_hsa_circ_256659,RMVar_hsa_circ_99600,RMVar_hsa_circ_123260,RMVar_hsa_circ_256660,RMVar_hsa_circ_256661,RMVar_hsa_circ_108558,RMVar_hsa_circ_80499,RMVar_hsa_circ_256662,RMVar_hsa_circ_256663,RMVar_hsa_circ_116269,RMVar_hsa_circ_256664,RMVar_hsa_circ_256665 10033 RMVar_ID_10033 Human_SNP_ID_397320741 A-to-I Human chr9 - 35702569 35702569 35702569 AGAATCGCTGGAACCCGGGAGGCAGAGGTTGCAGTGAGCCAAGATGGCGCCACTGCACTCCAGCC AGAATCGCTGGAACCCGGGAGGCAGAGGTTGCCGTGAGCCAAGATGGCGCCACTGCACTCCAGCC T G TLN1 Ensembl:ENSG00000137076 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1426610310 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76291,RMVar_hsa_circ_89989,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_97060,RMVar_hsa_circ_92285,RMVar_hsa_circ_256636,RMVar_hsa_circ_256644,RMVar_hsa_circ_83289,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_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,RMVar_hsa_circ_86505,RMVar_hsa_circ_80611,RMVar_hsa_circ_66996,RMVar_hsa_circ_94059,RMVar_hsa_circ_98509,RMVar_hsa_circ_256653,RMVar_hsa_circ_256654,RMVar_hsa_circ_114930,RMVar_hsa_circ_256656,RMVar_hsa_circ_104156,RMVar_hsa_circ_83504,RMVar_hsa_circ_256657,RMVar_hsa_circ_256658,RMVar_hsa_circ_256659,RMVar_hsa_circ_99600,RMVar_hsa_circ_123260,RMVar_hsa_circ_256660,RMVar_hsa_circ_256661,RMVar_hsa_circ_108558,RMVar_hsa_circ_78893,RMVar_hsa_circ_95584,RMVar_hsa_circ_80499,RMVar_hsa_circ_256662,RMVar_hsa_circ_256663,RMVar_hsa_circ_116269,RMVar_hsa_circ_121948,RMVar_hsa_circ_256664,RMVar_hsa_circ_256665,RMVar_hsa_circ_112606,RMVar_hsa_circ_88040,RMVar_hsa_circ_95373,RMVar_hsa_circ_85884,RMVar_hsa_circ_89487,RMVar_hsa_circ_101317,RMVar_hsa_circ_256669,RMVar_hsa_circ_256671,RMVar_hsa_circ_256673,RMVar_hsa_circ_78372,RMVar_hsa_circ_256672,RMVar_hsa_circ_256670,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_85206,RMVar_hsa_circ_85245,RMVar_hsa_circ_84239,RMVar_hsa_circ_256675,RMVar_hsa_circ_256679,RMVar_hsa_circ_256681,RMVar_hsa_circ_256683,RMVar_hsa_circ_80565,RMVar_hsa_circ_256682,RMVar_hsa_circ_256680,RMVar_hsa_circ_256677,RMVar_hsa_circ_256678,RMVar_hsa_circ_256676,RMVar_hsa_circ_256674 10034 RMVar_ID_10034 Human_SNP_ID_397320779 A-to-I Human chr9 - 35702686 35702685 35702686 GAGTTCGAGACCAGCCTGGCCAATATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCT GAGTTCGAGACCAGCCTGGCCAATATGGTGAA_CCCCGTCTCTACTAAAAATACAAAAATTAGCT GT G TLN1 Ensembl:ENSG00000137076 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1044922203 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_76291,RMVar_hsa_circ_89989,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_97060,RMVar_hsa_circ_92285,RMVar_hsa_circ_256636,RMVar_hsa_circ_256644,RMVar_hsa_circ_83289,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_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,RMVar_hsa_circ_86505,RMVar_hsa_circ_80611,RMVar_hsa_circ_66996,RMVar_hsa_circ_94059,RMVar_hsa_circ_98509,RMVar_hsa_circ_256653,RMVar_hsa_circ_256654,RMVar_hsa_circ_114930,RMVar_hsa_circ_256656,RMVar_hsa_circ_104156,RMVar_hsa_circ_83504,RMVar_hsa_circ_256657,RMVar_hsa_circ_256658,RMVar_hsa_circ_256659,RMVar_hsa_circ_99600,RMVar_hsa_circ_123260,RMVar_hsa_circ_256660,RMVar_hsa_circ_256661,RMVar_hsa_circ_108558,RMVar_hsa_circ_78893,RMVar_hsa_circ_95584,RMVar_hsa_circ_80499,RMVar_hsa_circ_256662,RMVar_hsa_circ_256663,RMVar_hsa_circ_116269,RMVar_hsa_circ_121948,RMVar_hsa_circ_256664,RMVar_hsa_circ_256665,RMVar_hsa_circ_112606,RMVar_hsa_circ_88040,RMVar_hsa_circ_95373,RMVar_hsa_circ_85884,RMVar_hsa_circ_89487,RMVar_hsa_circ_101317,RMVar_hsa_circ_256669,RMVar_hsa_circ_256671,RMVar_hsa_circ_256673,RMVar_hsa_circ_78372,RMVar_hsa_circ_256672,RMVar_hsa_circ_256670,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_85206,RMVar_hsa_circ_85245,RMVar_hsa_circ_84239,RMVar_hsa_circ_256675,RMVar_hsa_circ_256679,RMVar_hsa_circ_256681,RMVar_hsa_circ_256683,RMVar_hsa_circ_80565,RMVar_hsa_circ_256682,RMVar_hsa_circ_256680,RMVar_hsa_circ_256677,RMVar_hsa_circ_256678,RMVar_hsa_circ_256676,RMVar_hsa_circ_256674 10035 RMVar_ID_10035 Human_SNP_ID_397324245 A-to-I Human chr9 - 35714031 35714031 35714031 CCTTTGGAGATGGATTCTGCACTGAGTGTGGTACAGAATCTAGAGAAAGATCTACAGGAAGTGAA CCTTTGGAGATGGATTCTGCACTGAGTGTGGTGCAGAATCTAGAGAAAGATCTACAGGAAGTGAA T C TLN1 Ensembl:ENSG00000137076 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs772811817 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1705196 Human_Splice_Rec_1042404,Human_Splice_Rec_1042405 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 10036 RMVar_ID_10036 Human_SNP_ID_397331323 A-to-I Human chr9 - 35738740 35738740 35738740 GACATGTGGCCTGTGTGTCTAGTAAGGGATGCACATGCAGTGGCCAGTGTGCCAGGGGTATGGTT GACATGTGGCCTGTGTGTCTAGTAAGGGATGCGCATGCAGTGGCCAGTGTGCCAGGGGTATGGTT T C GBA2 Ensembl:ENSG00000070610 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs747280176 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61469 10037 RMVar_ID_10037 Human_SNP_ID_397337966 A-to-I Human chr9 + 35763735 35763735 35763735 GAAACCCTGTCTCTACTAAAAATACAAAAATTAGCCGAGTGTGGTGGTGTATGCCTGTTATCCTA GAAACCCTGTCTCTACTAAAAATACAAAAATTCGCCGAGTGTGGTGGTGTATGCCTGTTATCCTA A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs890203914 Functional Loss SNV dbSNP153 33..33 33 - - - 10038 RMVar_ID_10038 Human_SNP_ID_397337990 A-to-I Human chr9 + 35763877 35763877 35763877 GCACTCCAGTTTGGGCAACAGAGTGAGACTCCATCTCAAAAAAAAAAAAAAAAAAAGAAAAGAGA GCACTCCAGTTTGGGCAACAGAGTGAGACTCCGTCTCAAAAAAAAAAAAAAAAAAAGAAAAGAGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1291241376 Functional Loss SNV dbSNP153 33..33 33 - - - 10039 RMVar_ID_10039 Human_SNP_ID_397338383 A-to-I Human chr9 + 35765492 35765492 35765492 CAGCTTGGACAACATGGTGAAACCCCATCTCTACAAAAAATACAAAAATTAGTTGGGTGTGGTGG CAGCTTGGACAACATGGTGAAACCCCATCTCTCCAAAAAATACAAAAATTAGTTGGGTGTGGTGG A C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs916920541 Functional Loss SNV dbSNP153 33..33 33 - - - 10040 RMVar_ID_10040 Human_SNP_ID_397341256 A-to-I Human chr9 + 35778181 35778181 35778181 AAAATTGGCCGGGCGTGGTGGCGCATGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTGGCCGGGCGTGGTGGCGCATGCCTGTTATCCCAGCTACTCGGGAGGCTGAGGCAGGAGA A T AL133410.1 Ensembl:ENSG00000227388 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1014011789 Functional Loss SNV dbSNP153 33..33 33 - - - 10041 RMVar_ID_10041 Human_SNP_ID_397341849 A-to-I Human chr9 + 35780977 35780977 35780977 ATATCCATTGAGAAAACATTTATTTGAATTCTAAAATATACTGCCAATGTAAGGTACAAAGATTA ATATCCATTGAGAAAACATTTATTTGAATTCTCAAATATACTGCCAATGTAAGGTACAAAGATTA A C AL133410.1 Ensembl:ENSG00000227388 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900704549 Functional Loss SNV dbSNP153 33..33 33 - - - 10042 RMVar_ID_10042 Human_SNP_ID_397341850 A-to-I Human chr9 + 35780977 35780977 35780977 ATATCCATTGAGAAAACATTTATTTGAATTCTAAAATATACTGCCAATGTAAGGTACAAAGATTA ATATCCATTGAGAAAACATTTATTTGAATTCTGAAATATACTGCCAATGTAAGGTACAAAGATTA A G AL133410.1 Ensembl:ENSG00000227388 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900704549 Functional Loss SNV dbSNP153 33..33 33 - - - 10043 RMVar_ID_10043 Human_SNP_ID_397341852 A-to-I Human chr9 + 35780982 35780982 35780982 CATTGAGAAAACATTTATTTGAATTCTAAAATATACTGCCAATGTAAGGTACAAAGATTAAGGAC CATTGAGAAAACATTTATTTGAATTCTAAAATGTACTGCCAATGTAAGGTACAAAGATTAAGGAC A G AL133410.1 Ensembl:ENSG00000227388 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1023480816 Functional Loss SNV dbSNP153 33..33 33 - - - 10044 RMVar_ID_10044 Human_SNP_ID_397341984 A-to-I Human chr9 + 35781625 35781625 35781625 TTGGTTGTTAATCCTTGTACCTTGACACTGGCAATACCTTTTAGGTGTCAAATAAATGTCCTGAA TTGGTTGTTAATCCTTGTACCTTGACACTGGCGATACCTTTTAGGTGTCAAATAAATGTCCTGAA A G AL133410.1 Ensembl:ENSG00000227388 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs959834213 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17579261 10045 RMVar_ID_10045 Human_SNP_ID_397343491 A-to-I Human chr9 + 35788406 35788406 35788406 GCTGGCCAACATGGTGAAACGCTGTCTCTACTAAAAACAAAAATTAGCTGGGCATGGTGGCGGGC GCTGGCCAACATGGTGAAACGCTGTCTCTACTGAAAACAAAAATTAGCTGGGCATGGTGGCGGGC A G AL133410.1 Ensembl:ENSG00000227388 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1420419283 Functional Loss SNV dbSNP153 33..33 33 - - - 10046 RMVar_ID_10046 Human_SNP_ID_397343534 A-to-I Human chr9 + 35788529 35788529 35788529 TGGAGGTTGCAGTGAGCCGAGATTGCGCCACTACATTCCAGCCTGAGTAACAGAGTGAGACTCTG TGGAGGTTGCAGTGAGCCGAGATTGCGCCACTGCATTCCAGCCTGAGTAACAGAGTGAGACTCTG A G AL133410.1 Ensembl:ENSG00000227388 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs75145761 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26243243 10047 RMVar_ID_10047 Human_SNP_ID_397343687 A-to-I Human chr9 + 35789147 35789147 35789147 TCAAGCGGTTTTCCTGCCCCAGCCTCCCAAGTAGCTGGGATTACAGGTGCCCACCACCACGCCCA TCAAGCGGTTTTCCTGCCCCAGCCTCCCAAGTGGCTGGGATTACAGGTGCCCACCACCACGCCCA A G AL133410.1 Ensembl:ENSG00000227388 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1247945161 Functional Loss SNV dbSNP153 33..33 33 - - - 10048 RMVar_ID_10048 Human_SNP_ID_397421988 A-to-I Human chr9 + 36114789 36114789 36114789 ATTGCTTGAACCCGGGAGACAGAGGCTGCAGTAAGCCGAGATGGTGCCACTGCACTCCAGCCTGG ATTGCTTGAACCCGGGAGACAGAGGCTGCAGTTAGCCGAGATGGTGCCACTGCACTCCAGCCTGG A T RECK Ensembl:ENSG00000122707 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1206329899 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49327,RMVar_hsa_circ_346353 10049 RMVar_ID_10049 Human_SNP_ID_397442763 A-to-I Human chr9 + 36196421 36196421 36196421 CAGGCTGGAGTGCAGTGGCGCGATCTTGGCTCACTGCAACCTCTGCCTCCCGAGTTCAAGCAATT CAGGCTGGAGTGCAGTGGCGCGATCTTGGCTCCCTGCAACCTCTGCCTCCCGAGTTCAAGCAATT A C CLTA Ensembl:ENSG00000122705 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1009898549 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106208,RMVar_hsa_circ_256808 10050 RMVar_ID_10050 Human_SNP_ID_397442764 A-to-I Human chr9 + 36196421 36196421 36196421 CAGGCTGGAGTGCAGTGGCGCGATCTTGGCTCACTGCAACCTCTGCCTCCCGAGTTCAAGCAATT CAGGCTGGAGTGCAGTGGCGCGATCTTGGCTCGCTGCAACCTCTGCCTCCCGAGTTCAAGCAATT A G CLTA Ensembl:ENSG00000122705 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1009898549 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106208,RMVar_hsa_circ_256808 10051 RMVar_ID_10051 Human_SNP_ID_397443218 A-to-I Human chr9 + 36198198 36198198 36198198 TTTTGTATTTTTAGTAGAGATGGGGTTTCGCCATGTTGGCCAGGCAGGTCTTGAACTCCTGGGCT TTTTGTATTTTTAGTAGAGATGGGGTTTCGCCGTGTTGGCCAGGCAGGTCTTGAACTCCTGGGCT A G CLTA Ensembl:ENSG00000122705 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1489875729 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_256809,RMVar_hsa_circ_89874,RMVar_hsa_circ_106208,RMVar_hsa_circ_279692,RMVar_hsa_circ_256808,RMVar_hsa_circ_277520,RMVar_hsa_circ_256810,RMVar_hsa_circ_256811 10052 RMVar_ID_10052 Human_SNP_ID_397443307 A-to-I Human chr9 + 36198540 36198540 36198540 TCTGCTAAAAATACAAAAATTAACCAGGCGGTAGTGGCATGTGCCTGTAATCCCAGCTACTGGGG TCTGCTAAAAATACAAAAATTAACCAGGCGGTGGTGGCATGTGCCTGTAATCCCAGCTACTGGGG A G CLTA Ensembl:ENSG00000122705 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1215681488 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_256809,RMVar_hsa_circ_89874,RMVar_hsa_circ_106208,RMVar_hsa_circ_279692,RMVar_hsa_circ_256808,RMVar_hsa_circ_277520,RMVar_hsa_circ_256810,RMVar_hsa_circ_256811 10053 RMVar_ID_10053 Human_SNP_ID_397447382 A-to-I Human chr9 - 36215157 36215157 36215157 ACGCCCGGCTGATTTTTTTTTGTATTTTTAGTAGACAGGGTTTCACCATGTTGGCCAGGCTGGTC ACGCCCGGCTGATTTTTTTTTGTATTTTTAGTTGACAGGGTTTCACCATGTTGGCCAGGCTGGTC T A GNE Ensembl:ENSG00000159921 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1244358193 Functional Loss SNV dbSNP153 33..33 33 - - - 10054 RMVar_ID_10054 Human_SNP_ID_397447384 A-to-I Human chr9 - 36215166 36215166 36215166 ACATGCACCACGCCCGGCTGATTTTTTTTTGTATTTTTAGTAGACAGGGTTTCACCATGTTGGCC ACATGCACCACGCCCGGCTGATTTTTTTTTGTGTTTTTAGTAGACAGGGTTTCACCATGTTGGCC T C GNE Ensembl:ENSG00000159921 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170517420 Functional Loss SNV dbSNP153 33..33 33 - - - 10055 RMVar_ID_10055 Human_SNP_ID_397447933 A-to-I Human chr9 - 36216702 36216702 36216702 GCACCACTGCACTCCAGCCTGGGTGACAGAGCAAGACTCCATCTCAAAAATAATAATAATAAATA GCACCACTGCACTCCAGCCTGGGTGACAGAGCGAGACTCCATCTCAAAAATAATAATAATAAATA T C GNE Ensembl:ENSG00000159921 Protein coding 3'UTR GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831 HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line - 29129909,29796672,31158229,32596459 RNA-Seq:(High) rs1373838375 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_129043,Human_miRNA_ID_1266412 10056 RMVar_ID_10056 Human_SNP_ID_397447944 A-to-I Human chr9 - 36216765 36216765 36216765 CGGGAGGCTGAGGCAGGAGAATGGCATGAACCAGGGAGGCGGAGCTGGCAGTGAACTGAGACCGC CGGGAGGCTGAGGCAGGAGAATGGCATGAACCGGGGAGGCGGAGCTGGCAGTGAACTGAGACCGC T C GNE Ensembl:ENSG00000159921 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1020119404 Functional Loss SNV dbSNP153 33..33 33 - - - 10057 RMVar_ID_10057 Human_SNP_ID_397447950 A-to-I Human chr9 - 36216783 36216783 36216783 TGGCGGGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCATGAACCAGGGAGGCGGAGCTG TGGCGGGTCCCAGCTACTCGGGAGGCTGAGGCGGGAGAATGGCATGAACCAGGGAGGCGGAGCTG T C GNE Ensembl:ENSG00000159921 Protein coding 3'UTR GSE38233;GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;ASD brains,cerebellum;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,30559470,31158229 RNA-Seq:(High) rs999645453 Functional Loss SNV dbSNP153 33..33 33 - - - 10058 RMVar_ID_10058 Human_SNP_ID_397447978 A-to-I Human chr9 - 36216898 36216898 36216898 GGAGGCCGAGGCGGGCGGATCACGAGGTCAGGAGATCGAGACCGCCCTGGCTAACATGGTGAAAC GGAGGCCGAGGCGGGCGGATCACGAGGTCAGGTGATCGAGACCGCCCTGGCTAACATGGTGAAAC T A GNE Ensembl:ENSG00000159921 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs1459054326 Functional Loss SNV dbSNP153 33..33 33 - - - 10059 RMVar_ID_10059 Human_SNP_ID_397456956 A-to-I Human chr9 - 36255336 36255336 36255336 AGGCATGGTGGCGTGCGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATTGATTGAA AGGCATGGTGGCGTGCGCCTGTAATCCCAGCTCCTTGGGAGGCTGAGGCAGGAGAATTGATTGAA T G GNE Ensembl:ENSG00000159921 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1189079258 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80293,RMVar_hsa_circ_256818 10060 RMVar_ID_10060 Human_SNP_ID_397468888 A-to-I Human chr9 + 36301817 36301817 36301817 AGCATCTCAGCCATGTTGCCAAGGCTGGTCTCAAACTTCTGAGCTCAAGCAATCCTCCCGCCTAG AGCATCTCAGCCATGTTGCCAAGGCTGGTCTCGAACTTCTGAGCTCAAGCAATCCTCCCGCCTAG A G CLTA Ensembl:ENSG00000122705 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1358051507 Functional Loss SNV dbSNP153 33..33 33 - - - 10061 RMVar_ID_10061 Human_SNP_ID_397508009 A-to-I Human chr9 - 36448760 36448760 36448760 ACCTCAGGCAGTCCGCCCGCCTCTGTCTCCCAAAGTGCTGAGATTACAGGCTGAGCCACCGCGCC ACCTCAGGCAGTCCGCCCGCCTCTGTCTCCCAGAGTGCTGAGATTACAGGCTGAGCCACCGCGCC T C RNF38 Ensembl:ENSG00000137075 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1468209175 Functional Loss SNV dbSNP153 33..33 33 - - - 10062 RMVar_ID_10062 Human_SNP_ID_397509768 A-to-I Human chr9 - 36455128 36455128 36455128 TTGAGCCTGGGAGGCGGGGGTTGCAGTGAGCCAAGATCGCACCACCGCACTCTGCACATGGCGAC TTGAGCCTGGGAGGCGGGGGTTGCAGTGAGCCGAGATCGCACCACCGCACTCTGCACATGGCGAC T C RNF38 Ensembl:ENSG00000137075 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1377746053 Functional Loss SNV dbSNP153 33..33 33 - - - 10063 RMVar_ID_10063 Human_SNP_ID_397510724 A-to-I Human chr9 - 36459042 36459042 36459042 TACCACGCCCACCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGATGG TACCACGCCCACCTAATTTTTGTATTTTTAGTTGAGACAGGGTTTCACCATGTTGGCCAGGATGG T A RNF38 Ensembl:ENSG00000137075 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs374300307 Functional Loss SNV dbSNP153 33..33 33 - - - 10064 RMVar_ID_10064 Human_SNP_ID_397512380 A-to-I Human chr9 - 36465484 36465484 36465484 AAATCAGCCAGGCGTGGTGGCGTATGCCTGTAATCCCAGTTAGTCGGGAGGCTAAGGCAGGAGAA AAATCAGCCAGGCGTGGTGGCGTATGCCTGTAGTCCCAGTTAGTCGGGAGGCTAAGGCAGGAGAA T C RNF38 Ensembl:ENSG00000137075 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs541734795 Functional Loss SNV dbSNP153 33..33 33 - - - 10065 RMVar_ID_10065 Human_SNP_ID_397541829 A-to-I Human chr9 + 36574528 36574528 36574528 GGGAGGCTGAGGCACGAGCATCTCTGGAACCCAGGAGGCGGAGGTTGCGGTGAGCCGAGATCTAG GGGAGGCTGAGGCACGAGCATCTCTGGAACCCGGGAGGCGGAGGTTGCGGTGAGCCGAGATCTAG A G MELK Ensembl:ENSG00000165304 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs929543634 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16671799 10066 RMVar_ID_10066 Human_SNP_ID_397544397 A-to-I Human chr9 + 36584953 36584953 36584953 GTTGCCCAGGGTGGTCTCAAACTCCTGGCCTCAAGCAGTCTTCCCATCTCAGCTTCCCAAAGTAC GTTGCCCAGGGTGGTCTCAAACTCCTGGCCTCCAGCAGTCTTCCCATCTCAGCTTCCCAAAGTAC A C MELK Ensembl:ENSG00000165304 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs796363883 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29272,RMVar_hsa_circ_332766,RMVar_hsa_circ_342216,RMVar_hsa_circ_291611,RMVar_hsa_circ_274303,RMVar_hsa_circ_256855,RMVar_hsa_circ_256856,RMVar_hsa_circ_256857 10067 RMVar_ID_10067 Human_SNP_ID_397544398 A-to-I Human chr9 + 36584953 36584953 36584953 GTTGCCCAGGGTGGTCTCAAACTCCTGGCCTCAAGCAGTCTTCCCATCTCAGCTTCCCAAAGTAC GTTGCCCAGGGTGGTCTCAAACTCCTGGCCTCGAGCAGTCTTCCCATCTCAGCTTCCCAAAGTAC A G MELK Ensembl:ENSG00000165304 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs796363883 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29272,RMVar_hsa_circ_332766,RMVar_hsa_circ_342216,RMVar_hsa_circ_291611,RMVar_hsa_circ_274303,RMVar_hsa_circ_256855,RMVar_hsa_circ_256856,RMVar_hsa_circ_256857 10068 RMVar_ID_10068 Human_SNP_ID_397545696 A-to-I Human chr9 + 36589947 36589947 36589947 TTCTAGTTTTTTTTTTTTTTTTTTTGAGACGGAATTTCGCTCTGTCGCTCAGGCTGAAGTGCAGT TTCTAGTTTTTTTTTTTTTTTTTTTGAGACGGCATTTCGCTCTGTCGCTCAGGCTGAAGTGCAGT A C MELK Ensembl:ENSG00000165304 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1410201071 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16672094 RMVar_hsa_circ_29272,RMVar_hsa_circ_332766,RMVar_hsa_circ_342216,RMVar_hsa_circ_49712,RMVar_hsa_circ_256856,RMVar_hsa_circ_359433,RMVar_hsa_circ_376568,RMVar_hsa_circ_283985,RMVar_hsa_circ_256858 10069 RMVar_ID_10069 Human_SNP_ID_397546135 A-to-I Human chr9 + 36591867 36591867 36591867 CTCAGGTGAGGAGCCTGGGAGATATAGGCTACAGTGAGCTATGATTGCACCACTGCACTCCAGCC CTCAGGTGAGGAGCCTGGGAGATATAGGCTACGGTGAGCTATGATTGCACCACTGCACTCCAGCC A G MELK Ensembl:ENSG00000165304 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1352308197 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29272,RMVar_hsa_circ_332766,RMVar_hsa_circ_342216,RMVar_hsa_circ_49712,RMVar_hsa_circ_256856,RMVar_hsa_circ_359433,RMVar_hsa_circ_376568,RMVar_hsa_circ_283985,RMVar_hsa_circ_256858 10070 RMVar_ID_10070 Human_SNP_ID_397546638 A-to-I Human chr9 + 36593723 36593723 36593723 CTGTTGTTGTTTGTTTTTTGAGACGAAGTCTCACTTTGTCACCCAGGCTGGAGTGCAGTGGTGCA CTGTTGTTGTTTGTTTTTTGAGACGAAGTCTCCCTTTGTCACCCAGGCTGGAGTGCAGTGGTGCA A C MELK Ensembl:ENSG00000165304 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs543467245 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3900044 RMVar_hsa_circ_29272,RMVar_hsa_circ_332766,RMVar_hsa_circ_342216,RMVar_hsa_circ_49712,RMVar_hsa_circ_256856,RMVar_hsa_circ_359433,RMVar_hsa_circ_376568,RMVar_hsa_circ_283985,RMVar_hsa_circ_256858 10071 RMVar_ID_10071 Human_SNP_ID_397552905 A-to-I Human chr9 + 36616408 36616408 36616408 CATGTCAAACTCTTTTTTTTTTTTTTTTTTTTAAGGCAGAGCCTTACTTTGTCACCCAGGCTGGA CATGTCAAACTCTTTTTTTTTTTTTTTTTTTTTAGGCAGAGCCTTACTTTGTCACCCAGGCTGGA A T MELK Ensembl:ENSG00000165304 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1386569829 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29272,RMVar_hsa_circ_42918,RMVar_hsa_circ_47747,RMVar_hsa_circ_359433,RMVar_hsa_circ_376568,RMVar_hsa_circ_341101,RMVar_hsa_circ_347759,RMVar_hsa_circ_316446,RMVar_hsa_circ_39111,RMVar_hsa_circ_289308,RMVar_hsa_circ_335019,RMVar_hsa_circ_348829,RMVar_hsa_circ_329762,RMVar_hsa_circ_347886,RMVar_hsa_circ_256861,RMVar_hsa_circ_256862,RMVar_hsa_circ_374417,RMVar_hsa_circ_55804,RMVar_hsa_circ_51133,RMVar_hsa_circ_256863,RMVar_hsa_circ_339349,RMVar_hsa_circ_68024 10072 RMVar_ID_10072 Human_SNP_ID_397555974 A-to-I Human chr9 + 36629056 36629056 36629056 GCCCAGCTAATTTTTGTATTTTTAGTAGAAACAAGGTTTCCCTGTGTCAGCCAGGATGGTCTTGA GCCCAGCTAATTTTTGTATTTTTAGTAGAAACTAGGTTTCCCTGTGTCAGCCAGGATGGTCTTGA A T MELK Ensembl:ENSG00000165304 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs766500268 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29272,RMVar_hsa_circ_42918,RMVar_hsa_circ_47747,RMVar_hsa_circ_359433,RMVar_hsa_circ_376568,RMVar_hsa_circ_341101,RMVar_hsa_circ_347759,RMVar_hsa_circ_316446,RMVar_hsa_circ_39111,RMVar_hsa_circ_289308,RMVar_hsa_circ_335019,RMVar_hsa_circ_348829,RMVar_hsa_circ_329762,RMVar_hsa_circ_347886,RMVar_hsa_circ_256861,RMVar_hsa_circ_256862,RMVar_hsa_circ_374417,RMVar_hsa_circ_55804,RMVar_hsa_circ_51133,RMVar_hsa_circ_256863,RMVar_hsa_circ_339349,RMVar_hsa_circ_68024 10073 RMVar_ID_10073 Human_SNP_ID_397557530 A-to-I Human chr9 + 36635498 36635498 36635498 GTTGGCCAGGCTGGTCTTGAACTCCTGACCTCAGGTGGTCCGCCTGCCTTGGCCTCCCAAAATGC GTTGGCCAGGCTGGTCTTGAACTCCTGACCTCTGGTGGTCCGCCTGCCTTGGCCTCCCAAAATGC A T MELK Ensembl:ENSG00000165304 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1240708254 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29272,RMVar_hsa_circ_42918,RMVar_hsa_circ_47747,RMVar_hsa_circ_359433,RMVar_hsa_circ_376568,RMVar_hsa_circ_341101,RMVar_hsa_circ_347759,RMVar_hsa_circ_39111,RMVar_hsa_circ_289308,RMVar_hsa_circ_335019,RMVar_hsa_circ_348829,RMVar_hsa_circ_256861,RMVar_hsa_circ_256862,RMVar_hsa_circ_374417,RMVar_hsa_circ_55804,RMVar_hsa_circ_256863,RMVar_hsa_circ_339349,RMVar_hsa_circ_316666,RMVar_hsa_circ_341574,RMVar_hsa_circ_332034,RMVar_hsa_circ_343536 10074 RMVar_ID_10074 Human_SNP_ID_397561746 A-to-I Human chr9 + 36652327 36652327 36652327 CCTCGGCCTCCCAAAGTGCTGGGATTATAGGCATGAGCCACCGTGCCCGGCCTCTAAAATTCTGA CCTCGGCCTCCCAAAGTGCTGGGATTATAGGCGTGAGCCACCGTGCCCGGCCTCTAAAATTCTGA A G MELK Ensembl:ENSG00000165304 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs989605125 Functional Loss SNV dbSNP153 33..33 33 - - - 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 10075 RMVar_ID_10075 Human_SNP_ID_397561808 A-to-I Human chr9 + 36652619 36652619 36652619 AGGCGTGGTGATGAGTGCCTGTAGTCCCAGCTACTTGGGAGGATGAGGCAGGAGAATCGCTTGAA AGGCGTGGTGATGAGTGCCTGTAGTCCCAGCTGCTTGGGAGGATGAGGCAGGAGAATCGCTTGAA A G MELK Ensembl:ENSG00000165304 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1554735363 Functional Loss SNV dbSNP153 33..33 33 - - - 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 10076 RMVar_ID_10076 Human_SNP_ID_397567841 A-to-I Human chr9 + 36678596 36678595 36678597 ACCCAGCAAATTTTTTTACTTTTTGTACAGACAGGGTCTCACTATGCTGCCCAGGCTGATCTCAA ACCCAGCAAATTTTTTTACTTTTTGTACAGAC__GGTCTCACTATGCTGCCCAGGCTGATCTCAA CAG C RF00017-4495,RF00017-5280 RNACentral:URS0000923EDC,RNACentral:URS0000976B19 SRP RNA,SRP RNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs931209654 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_16673694 10077 RMVar_ID_10077 Human_SNP_ID_397567974 A-to-I Human chr9 + 36679159 36679159 36679159 TCTCTACTAAGAACACAAAAAAGTAGCTAGGTATGGTGGCATGTGGCTGTAATCCCACCTACTTG TCTCTACTAAGAACACAAAAAAGTAGCTAGGTGTGGTGGCATGTGGCTGTAATCCCACCTACTTG A G RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1363228312 Functional Loss SNV dbSNP153 33..33 33 - - - 10078 RMVar_ID_10078 Human_SNP_ID_397681741 A-to-I Human chr9 + 37133064 37133064 37133064 GCTGAGGCAGGAGAATCGCTTGAACCTGGGAGACGGAGGTTGCAGTGAGCCGAGATCGTGCCACT GCTGAGGCAGGAGAATCGCTTGAACCTGGGAGGCGGAGGTTGCAGTGAGCCGAGATCGTGCCACT A G ZCCHC7 Ensembl:ENSG00000147905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs889332215 Functional Loss SNV dbSNP153 33..33 33 - - - 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_256888,RMVar_hsa_circ_256889,RMVar_hsa_circ_256887,RMVar_hsa_circ_256884,RMVar_hsa_circ_256885,RMVar_hsa_circ_256883 10079 RMVar_ID_10079 Human_SNP_ID_397682590 A-to-I Human chr9 + 37136570 37136570 37136570 GCCTTGACCTCCCGGGCTGAAGTGATCCTCCTACCTCAACCTCCCAGGTAGCTGAGACTGCAGAT GCCTTGACCTCCCGGGCTGAAGTGATCCTCCTGCCTCAACCTCCCAGGTAGCTGAGACTGCAGAT A G ZCCHC7 Ensembl:ENSG00000147905 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1564135306 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16674526 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_256888,RMVar_hsa_circ_256889,RMVar_hsa_circ_256887,RMVar_hsa_circ_256884,RMVar_hsa_circ_256885,RMVar_hsa_circ_256883 10080 RMVar_ID_10080 Human_SNP_ID_397682633 A-to-I Human chr9 + 37136751 37136751 37136751 GCCCACCTCAGCCTCCCAAAGTGCTGGGATTTACAGGTGTGAGTCACCGCCCTGGCCCCACTTGA GCCCACCTCAGCCTCCCAAAGTGCTGGGATTTGCAGGTGTGAGTCACCGCCCTGGCCCCACTTGA A G ZCCHC7 Ensembl:ENSG00000147905 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs528836252 Functional Loss SNV dbSNP153 33..33 33 - - - 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_256888,RMVar_hsa_circ_256889,RMVar_hsa_circ_256887,RMVar_hsa_circ_256884,RMVar_hsa_circ_256885,RMVar_hsa_circ_256883 10081 RMVar_ID_10081 Human_SNP_ID_397687090 A-to-I Human chr9 + 37157043 37157043 37157043 AGTAAGATGTGGTTTTCTGTTATCATTGTTTTAGTGTTTGTACTGATAATGTGGAAGCAAACACC AGTAAGATGTGGTTTTCTGTTATCATTGTTTTGGTGTTTGTACTGATAATGTGGAAGCAAACACC A G ZCCHC7 Ensembl:ENSG00000147905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs768281798 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2525107 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_256888,RMVar_hsa_circ_256887,RMVar_hsa_circ_256884,RMVar_hsa_circ_256885,RMVar_hsa_circ_356455,RMVar_hsa_circ_256883 10082 RMVar_ID_10082 Human_SNP_ID_397687851 A-to-I Human chr9 + 37160319 37160319 37160319 ATCATTTGAGCCCAGGAGTTTGAGATCAGCCCAGGCAACATAGCGAGACTTCATCTCTACTAAAA ATCATTTGAGCCCAGGAGTTTGAGATCAGCCCGGGCAACATAGCGAGACTTCATCTCTACTAAAA A G ZCCHC7 Ensembl:ENSG00000147905 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs572044130 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2553712 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_256888,RMVar_hsa_circ_256887,RMVar_hsa_circ_256884,RMVar_hsa_circ_256885,RMVar_hsa_circ_356455,RMVar_hsa_circ_256883 10083 RMVar_ID_10083 Human_SNP_ID_397687887 A-to-I Human chr9 + 37160394 37160394 37160394 AAAATTAGCCAGGCGTGGTGGGGTGTGCCTGTATTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA AAAATTAGCCAGGCGTGGTGGGGTGTGCCTGTGTTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA A G ZCCHC7 Ensembl:ENSG00000147905 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs111435228 Functional Loss SNV dbSNP153 33..33 33 - - - 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_256888,RMVar_hsa_circ_256887,RMVar_hsa_circ_256884,RMVar_hsa_circ_256885,RMVar_hsa_circ_356455,RMVar_hsa_circ_256883 10084 RMVar_ID_10084 Human_SNP_ID_397687939 A-to-I Human chr9 + 37160629 37160629 37160629 TTAACATGGGCTGGGGGCAGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCGAGGCAGGTG TTAACATGGGCTGGGGGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCGAGGCAGGTG A G ZCCHC7 Ensembl:ENSG00000147905 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1040080750 Functional Loss SNV dbSNP153 33..33 33 - - - 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_256888,RMVar_hsa_circ_256887,RMVar_hsa_circ_256884,RMVar_hsa_circ_256885,RMVar_hsa_circ_356455,RMVar_hsa_circ_256883 10085 RMVar_ID_10085 Human_SNP_ID_397687968 A-to-I Human chr9 + 37160749 37160749 37160749 CTGTACTCAAAATACAAAAATTAGCCGGGTGTAGTAGCTGGTGCCGGTAATCCCAACTACTCGGG CTGTACTCAAAATACAAAAATTAGCCGGGTGTGGTAGCTGGTGCCGGTAATCCCAACTACTCGGG A G ZCCHC7 Ensembl:ENSG00000147905 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1032430120 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17579265 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_256888,RMVar_hsa_circ_256887,RMVar_hsa_circ_256884,RMVar_hsa_circ_256885,RMVar_hsa_circ_356455,RMVar_hsa_circ_256883 10086 RMVar_ID_10086 Human_SNP_ID_397688066 A-to-I Human chr9 + 37161062 37161062 37161062 CTCTCCACCTCCTGGGTTCAAGCAGTTCTCTTATCTCAGCCTCCCGAGTAGCTGGGATTACAGGC CTCTCCACCTCCTGGGTTCAAGCAGTTCTCTTTTCTCAGCCTCCCGAGTAGCTGGGATTACAGGC A T ZCCHC7 Ensembl:ENSG00000147905 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs927241557 Functional Loss SNV dbSNP153 33..33 33 - - - 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_256888,RMVar_hsa_circ_256887,RMVar_hsa_circ_256884,RMVar_hsa_circ_256885,RMVar_hsa_circ_356455,RMVar_hsa_circ_256883 10087 RMVar_ID_10087 Human_SNP_ID_397688084 A-to-I Human chr9 + 37161115 37161115 37161115 GGGATTACAGGCACAGGCCACCACAACTGGCTAATTTTTGTATTTTTAGTGGAGACAGGGTTTCA GGGATTACAGGCACAGGCCACCACAACTGGCTGATTTTTGTATTTTTAGTGGAGACAGGGTTTCA A G ZCCHC7 Ensembl:ENSG00000147905 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs936643361 Functional Loss SNV dbSNP153 33..33 33 - - - 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_256888,RMVar_hsa_circ_256887,RMVar_hsa_circ_256884,RMVar_hsa_circ_256885,RMVar_hsa_circ_356455,RMVar_hsa_circ_256883 10088 RMVar_ID_10088 Human_SNP_ID_397688166 A-to-I Human chr9 + 37161402 37161402 37161402 CGAGACCATCCTGGCTAACACGGTGAAACCCCATCTCTACTAAAAATACAAAAAAATTAGCCAGA CGAGACCATCCTGGCTAACACGGTGAAACCCCGTCTCTACTAAAAATACAAAAAAATTAGCCAGA A G ZCCHC7 Ensembl:ENSG00000147905 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs961650865 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_183207 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_256888,RMVar_hsa_circ_256887,RMVar_hsa_circ_256884,RMVar_hsa_circ_256885,RMVar_hsa_circ_356455,RMVar_hsa_circ_256883 10089 RMVar_ID_10089 Human_SNP_ID_397688207 A-to-I Human chr9 + 37161524 37161524 37161524 ATGAACCTGGCAGGCGGAGCTTGCAGTGAGCCAAGATGGCGTCACTGCACTCCAGCCTGAGGGAC ATGAACCTGGCAGGCGGAGCTTGCAGTGAGCCGAGATGGCGTCACTGCACTCCAGCCTGAGGGAC A G ZCCHC7 Ensembl:ENSG00000147905 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs562600932 Functional Loss SNV dbSNP153 33..33 33 - - - 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_256888,RMVar_hsa_circ_256887,RMVar_hsa_circ_256884,RMVar_hsa_circ_256885,RMVar_hsa_circ_356455,RMVar_hsa_circ_256883 10090 RMVar_ID_10090 Human_SNP_ID_397689076 A-to-I Human chr9 + 37164635 37164635 37164635 ACAGGGTCTCCCTCTATTGCCCAGGCTGGAGTACATTGGCATGATCATGGCTTACTGCAGCCTTG ACAGGGTCTCCCTCTATTGCCCAGGCTGGAGTGCATTGGCATGATCATGGCTTACTGCAGCCTTG A G ZCCHC7 Ensembl:ENSG00000147905 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1397596983 Functional Loss SNV dbSNP153 33..33 33 - - - 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_256888,RMVar_hsa_circ_256887,RMVar_hsa_circ_256884,RMVar_hsa_circ_256885,RMVar_hsa_circ_356455,RMVar_hsa_circ_256883 10091 RMVar_ID_10091 Human_SNP_ID_397689109 A-to-I Human chr9 + 37164775 37164775 37164775 TTTTTTTTAGGTATTTATTCACTCTGTGGTCCAGGCTGGTCCCAAACTCCTGGGTTCAAGAGATC TTTTTTTTAGGTATTTATTCACTCTGTGGTCCGGGCTGGTCCCAAACTCCTGGGTTCAAGAGATC A G ZCCHC7 Ensembl:ENSG00000147905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs899370101 Functional Loss SNV dbSNP153 33..33 33 - - - 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_256888,RMVar_hsa_circ_256887,RMVar_hsa_circ_256884,RMVar_hsa_circ_256885,RMVar_hsa_circ_356455,RMVar_hsa_circ_256883 10092 RMVar_ID_10092 Human_SNP_ID_397691618 A-to-I Human chr9 + 37175494 37175494 37175494 GGGAGGCCGAGATAGGCGGGTCACTTGAGTCCAGGAGTTTGAGGCCAGTCTGACCAACATGGTGA GGGAGGCCGAGATAGGCGGGTCACTTGAGTCCGGGAGTTTGAGGCCAGTCTGACCAACATGGTGA A G ZCCHC7 Ensembl:ENSG00000147905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1320025214 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_183209 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 10093 RMVar_ID_10093 Human_SNP_ID_397695328 A-to-I Human chr9 + 37190835 37190835 37190835 GAAGTCAGGAGTTCGAGACCAGCCTGACCAACATGGAAAAACCCTGTCTCTACTAAAAAAAAATA GAAGTCAGGAGTTCGAGACCAGCCTGACCAACCTGGAAAAACCCTGTCTCTACTAAAAAAAAATA A C ZCCHC7 Ensembl:ENSG00000147905 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1564168710 Functional Loss SNV dbSNP153 33..33 33 - - - 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 10094 RMVar_ID_10094 Human_SNP_ID_397699617 A-to-I Human chr9 + 37208197 37208197 37208197 TCCTCGACCTCCTGGGCTCAGGTGATCCTCCCACCTCATCCCCTCGAATAGCTGAGATTACAGGC TCCTCGACCTCCTGGGCTCAGGTGATCCTCCCGCCTCATCCCCTCGAATAGCTGAGATTACAGGC A G ZCCHC7 Ensembl:ENSG00000147905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs776963272 Functional Loss SNV dbSNP153 33..33 33 - - - 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 10095 RMVar_ID_10095 Human_SNP_ID_397704547 A-to-I Human chr9 + 37228965 37228965 37228965 TCAAGCAGTTCTCCTGCCTCAGCCTCTCGAGTAGCTGGGACTATAGGCGCCTGCCACCATGCCCG TCAAGCAGTTCTCCTGCCTCAGCCTCTCGAGTGGCTGGGACTATAGGCGCCTGCCACCATGCCCG A G ZCCHC7 Ensembl:ENSG00000147905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1406081043 Functional Loss SNV dbSNP153 33..33 33 - - - 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 10096 RMVar_ID_10096 Human_SNP_ID_397712725 A-to-I Human chr9 + 37266753 37266753 37266753 AAAATTAACCAGGTATAGTGGTACACACCTGTAATCTTAGCTACTTGGGGGGCTAAGGTTGGAGG AAAATTAACCAGGTATAGTGGTACACACCTGTGATCTTAGCTACTTGGGGGGCTAAGGTTGGAGG A G ZCCHC7 Ensembl:ENSG00000147905 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1460901807 Functional Loss SNV dbSNP153 33..33 33 - - - 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_99939,RMVar_hsa_circ_20977,RMVar_hsa_circ_256884,RMVar_hsa_circ_256885,RMVar_hsa_circ_356455,RMVar_hsa_circ_256883 10097 RMVar_ID_10097 Human_SNP_ID_397713446 A-to-I Human chr9 + 37269498 37269498 37269498 AAAATTAACTGAGTGTTGCAGTGCGTGCCTATAGTCCCAGCTACCAGGGAGGCTGAGGCAGGAGG AAAATTAACTGAGTGTTGCAGTGCGTGCCTATCGTCCCAGCTACCAGGGAGGCTGAGGCAGGAGG A C ZCCHC7 Ensembl:ENSG00000147905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs527607025 Functional Loss SNV dbSNP153 33..33 33 - - - 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_99939,RMVar_hsa_circ_20977,RMVar_hsa_circ_256884,RMVar_hsa_circ_256885,RMVar_hsa_circ_356455,RMVar_hsa_circ_256883 10098 RMVar_ID_10098 Human_SNP_ID_397713447 A-to-I Human chr9 + 37269498 37269498 37269498 AAAATTAACTGAGTGTTGCAGTGCGTGCCTATAGTCCCAGCTACCAGGGAGGCTGAGGCAGGAGG AAAATTAACTGAGTGTTGCAGTGCGTGCCTATGGTCCCAGCTACCAGGGAGGCTGAGGCAGGAGG A G ZCCHC7 Ensembl:ENSG00000147905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs527607025 Functional Loss SNV dbSNP153 33..33 33 - - - 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_99939,RMVar_hsa_circ_20977,RMVar_hsa_circ_256884,RMVar_hsa_circ_256885,RMVar_hsa_circ_356455,RMVar_hsa_circ_256883 10099 RMVar_ID_10099 Human_SNP_ID_397713448 A-to-I Human chr9 + 37269498 37269498 37269498 AAAATTAACTGAGTGTTGCAGTGCGTGCCTATAGTCCCAGCTACCAGGGAGGCTGAGGCAGGAGG AAAATTAACTGAGTGTTGCAGTGCGTGCCTATTGTCCCAGCTACCAGGGAGGCTGAGGCAGGAGG A T ZCCHC7 Ensembl:ENSG00000147905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs527607025 Functional Loss SNV dbSNP153 33..33 33 - - - 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_99939,RMVar_hsa_circ_20977,RMVar_hsa_circ_256884,RMVar_hsa_circ_256885,RMVar_hsa_circ_356455,RMVar_hsa_circ_256883 10100 RMVar_ID_10100 Human_SNP_ID_397724684 A-to-I Human chr9 + 37315884 37315884 37315884 AGGTAAAAGTTCTATATAAGCATCCCTAAACCAGGGAAGGTAGTAGTGGGTAGCAAGGGTGATGA AGGTAAAAGTTCTATATAAGCATCCCTAAACCGGGGAAGGTAGTAGTGGGTAGCAAGGGTGATGA A G ZCCHC7 Ensembl:ENSG00000147905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1158051786 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38298,RMVar_hsa_circ_122994,RMVar_hsa_circ_256878,RMVar_hsa_circ_270512,RMVar_hsa_circ_306931,RMVar_hsa_circ_99939,RMVar_hsa_circ_20977,RMVar_hsa_circ_256895,RMVar_hsa_circ_256884,RMVar_hsa_circ_256883,RMVar_hsa_circ_360266,RMVar_hsa_circ_374824,RMVar_hsa_circ_278993,RMVar_hsa_circ_256896,RMVar_hsa_circ_256894,RMVar_hsa_circ_268956,RMVar_hsa_circ_267733,RMVar_hsa_circ_75618,RMVar_hsa_circ_303092,RMVar_hsa_circ_92654,RMVar_hsa_circ_256900,RMVar_hsa_circ_256901,RMVar_hsa_circ_256899 10101 RMVar_ID_10101 Human_SNP_ID_397753561 A-to-I Human chr9 + 37432555 37432555 37432555 CAAAAATTAGCCAGGTATGGTGGTGCATGCCTATAGTCCCAGCTGTTTGGGAGGCTGAGGCAGAA CAAAAATTAGCCAGGTATGGTGGTGCATGCCTGTAGTCCCAGCTGTTTGGGAGGCTGAGGCAGAA A G GRHPR Ensembl:ENSG00000137106 Protein coding intron GSE38233;GSE100210;GSE99789 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 24183664,29129909,29796672 RNA-Seq:(High) rs1022939787 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1044578 RMVar_hsa_circ_122450,RMVar_hsa_circ_256905,RMVar_hsa_circ_96599,RMVar_hsa_circ_256916 10102 RMVar_ID_10102 Human_SNP_ID_397753780 A-to-I Human chr9 + 37433395 37433395 37433395 AGCTGGGATTACAGGCGTGTACCACCAGGCCCAGCCAATTTTTGTATTTTTAGTAGAGATGGGGT AGCTGGGATTACAGGCGTGTACCACCAGGCCCGGCCAATTTTTGTATTTTTAGTAGAGATGGGGT A G GRHPR Ensembl:ENSG00000137106 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941906152 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122450,RMVar_hsa_circ_256905,RMVar_hsa_circ_96599,RMVar_hsa_circ_256916 10103 RMVar_ID_10103 Human_SNP_ID_397753811 A-to-I Human chr9 + 37433494 37433494 37433494 GACCTCAGATGGTCCACCTGCCTCTGCCTCCCAAAGTGCTGGGATTACAGGCATGAGTGTCCGGC GACCTCAGATGGTCCACCTGCCTCTGCCTCCCGAAGTGCTGGGATTACAGGCATGAGTGTCCGGC A G GRHPR Ensembl:ENSG00000137106 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1256036169 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122450,RMVar_hsa_circ_256905,RMVar_hsa_circ_96599,RMVar_hsa_circ_256916 10104 RMVar_ID_10104 Human_SNP_ID_397754241 A-to-I Human chr9 + 37435068 37435068 37435068 AAGACCAAGAGTTCGAATCTAGCCTGGGCAACATAGTGAAACCCCATCCCTATAAAAAATAAAAA AAGACCAAGAGTTCGAATCTAGCCTGGGCAACCTAGTGAAACCCCATCCCTATAAAAAATAAAAA A C GRHPR Ensembl:ENSG00000137106 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs992275849 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122450,RMVar_hsa_circ_256905,RMVar_hsa_circ_96599,RMVar_hsa_circ_256916 10105 RMVar_ID_10105 Human_SNP_ID_397754242 A-to-I Human chr9 + 37435068 37435068 37435068 AAGACCAAGAGTTCGAATCTAGCCTGGGCAACATAGTGAAACCCCATCCCTATAAAAAATAAAAA AAGACCAAGAGTTCGAATCTAGCCTGGGCAACGTAGTGAAACCCCATCCCTATAAAAAATAAAAA A G GRHPR Ensembl:ENSG00000137106 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs992275849 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122450,RMVar_hsa_circ_256905,RMVar_hsa_circ_96599,RMVar_hsa_circ_256916 10106 RMVar_ID_10106 Human_SNP_ID_397754243 A-to-I Human chr9 + 37435070 37435070 37435070 GACCAAGAGTTCGAATCTAGCCTGGGCAACATAGTGAAACCCCATCCCTATAAAAAATAAAAAAT GACCAAGAGTTCGAATCTAGCCTGGGCAACATGGTGAAACCCCATCCCTATAAAAAATAAAAAAT A G GRHPR Ensembl:ENSG00000137106 Protein coding intron GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs555013678 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122450,RMVar_hsa_circ_256905,RMVar_hsa_circ_96599,RMVar_hsa_circ_256916 10107 RMVar_ID_10107 Human_SNP_ID_397754262 A-to-I Human chr9 + 37435176 37435176 37435176 AGGAGGCTGAAGTGGGAGGATCACTTGAGCCTAGGAGGTTGAGGCTGTAGTAAGCTGACTATGCC AGGAGGCTGAAGTGGGAGGATCACTTGAGCCTTGGAGGTTGAGGCTGTAGTAAGCTGACTATGCC A T GRHPR Ensembl:ENSG00000137106 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1486497164 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16678874 RMVar_hsa_circ_122450,RMVar_hsa_circ_256905,RMVar_hsa_circ_96599,RMVar_hsa_circ_256916 10108 RMVar_ID_10108 Human_SNP_ID_397757118 A-to-I Human chr9 + 37445578 37445578 37445578 GAGGCTGAGGGGGATCACTTGAGCCCGGAGTCAGAACTTGCAGTGAGCAGAGATCACGTCACTGC GAGGCTGAGGGGGATCACTTGAGCCCGGAGTCGGAACTTGCAGTGAGCAGAGATCACGTCACTGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947781313 Functional Loss SNV dbSNP153 33..33 33 - - - 10109 RMVar_ID_10109 Human_SNP_ID_397771678 A-to-I Human chr9 + 37503349 37503349 37503349 CCTGAAATCCCAGCACTTTGGGAGGCCGAGGCAGGAAGATCATTGAGCTCAGGAGTTTGAAACCA CCTGAAATCCCAGCACTTTGGGAGGCCGAGGCGGGAAGATCATTGAGCTCAGGAGTTTGAAACCA A G POLR1E Ensembl:ENSG00000137054 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1128853 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16679647,Human_RBP_ID_18136202,Human_RBP_ID_26565771 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 10110 RMVar_ID_10110 Human_SNP_ID_397771729 A-to-I Human chr9 + 37503493 37503493 37503493 CCAGCTACTCGGGAGGCTGAGGCAGGACGATTACTTGAGCTTGGGAAATCAAGGTTGCAGTGAGC CCAGCTACTCGGGAGGCTGAGGCAGGACGATTGCTTGAGCTTGGGAAATCAAGGTTGCAGTGAGC A G POLR1E Ensembl:ENSG00000137054 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-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 10111 RMVar_ID_10111 Human_SNP_ID_397771930 A-to-I Human chr9 + 37504417 37504416 37504418 CTTTCTTCTTTTTCTTTTTATTTTTTTGAGACAGAGTCTTGCTCTGTAGCCCAGGCTGGAGTGCA CTTTCTTCTTTTTCTTTTTATTTTTTTGAGAC__AGTCTTGCTCTGTAGCCCAGGCTGGAGTGCA CAG C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1426148405 Functional Loss DEL dbSNP153 33..34 33 - - - 10112 RMVar_ID_10112 Human_SNP_ID_397772186 A-to-I Human chr9 + 37505500 37505497 37505501 GTTTCCGTGATTACTTTTTTTTTTTGAGATGGAGTTTCGCTCTTGTTGCCCAGGCTGGAGTGCAA GTTTCCGTGATTACTTTTTTTTTTTGAGAT____TTTCGCTCTTGTTGCCCAGGCTGGAGTGCAA TGGAG T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1564327750 Functional Loss DEL dbSNP153 31..34 33 - - - 10113 RMVar_ID_10113 Human_SNP_ID_397772188 A-to-I Human chr9 + 37505500 37505500 37505500 GTTTCCGTGATTACTTTTTTTTTTTGAGATGGAGTTTCGCTCTTGTTGCCCAGGCTGGAGTGCAA GTTTCCGTGATTACTTTTTTTTTTTGAGATGGTGTTTCGCTCTTGTTGCCCAGGCTGGAGTGCAA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1484938800 Functional Loss SNV dbSNP153 33..33 33 - - - 10114 RMVar_ID_10114 Human_SNP_ID_397772227 A-to-I Human chr9 + 37505645 37505645 37505645 GCACCACCATGCCCGGCTAATTTTGTATTTTTAGTAGAGACAGCGTTTCTCCATGTTAGGCTGGT GCACCACCATGCCCGGCTAATTTTGTATTTTTGGTAGAGACAGCGTTTCTCCATGTTAGGCTGGT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971066977 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16679726 10115 RMVar_ID_10115 Human_SNP_ID_397772230 A-to-I Human chr9 + 37505654 37505654 37505654 TGCCCGGCTAATTTTGTATTTTTAGTAGAGACAGCGTTTCTCCATGTTAGGCTGGTCTCAATCTC TGCCCGGCTAATTTTGTATTTTTAGTAGAGACTGCGTTTCTCCATGTTAGGCTGGTCTCAATCTC A T - - Other Unknown GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1309079301 Functional Loss SNV dbSNP153 33..33 33 - - - 10116 RMVar_ID_10116 Human_SNP_ID_397772239 A-to-I Human chr9 + 37505681 37505681 37505681 GAGACAGCGTTTCTCCATGTTAGGCTGGTCTCAATCTCCTGACCTCAGGTGATCTGCCCGCCTCG GAGACAGCGTTTCTCCATGTTAGGCTGGTCTCGATCTCCTGACCTCAGGTGATCTGCCCGCCTCG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1013306726 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16679727 10117 RMVar_ID_10117 Human_SNP_ID_397772253 A-to-I Human chr9 + 37505722 37505722 37505722 ACCTCAGGTGATCTGCCCGCCTCGGTCTCCCAAAGTGCTGGAATTATAGGCGTGAGCCACCACGC ACCTCAGGTGATCTGCCCGCCTCGGTCTCCCAGAGTGCTGGAATTATAGGCGTGAGCCACCACGC A G - - Other Unknown GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1204167127 Functional Loss SNV dbSNP153 33..33 33 - - - 10118 RMVar_ID_10118 Human_SNP_ID_397773170 A-to-I Human chr9 + 37510059 37510059 37510059 CATTAGGTAACAAACTAAAGAAATCTGAGGCCAGGCACAGTGGCTCATGTTTGTAATCCCAGCAC CATTAGGTAACAAACTAAAGAAATCTGAGGCCGGGCACAGTGGCTCATGTTTGTAATCCCAGCAC A G AL513165.1 Ensembl:ENSG00000234160 lincRNA intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1422231508 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16679925,Human_RBP_ID_24303433 10119 RMVar_ID_10119 Human_SNP_ID_397773187 A-to-I Human chr9 + 37510141 37510141 37510141 GGCGGATCACTTGAGCCCAGGAGTTTGAGACCAGGCTAGGCAACATGGCAAAACCCCGTCTCTAC GGCGGATCACTTGAGCCCAGGAGTTTGAGACCGGGCTAGGCAACATGGCAAAACCCCGTCTCTAC A G AL513165.1 Ensembl:ENSG00000234160 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1452839542 Functional Loss SNV dbSNP153 33..33 33 - - - 10120 RMVar_ID_10120 Human_SNP_ID_397773199 A-to-I Human chr9 + 37510191 37510191 37510191 AAACCCCGTCTCTACAAAAAAATACATAAATTAGCCAGGCGTGGTGGTGCATGCCTGTAGTCCCA AAACCCCGTCTCTACAAAAAAATACATAAATTGGCCAGGCGTGGTGGTGCATGCCTGTAGTCCCA A G AL513165.1 Ensembl:ENSG00000234160 lincRNA intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1138840 Functional Loss SNV dbSNP153 33..33 33 - - - 10121 RMVar_ID_10121 Human_SNP_ID_397773200 A-to-I Human chr9 + 37510195 37510195 37510195 CCCGTCTCTACAAAAAAATACATAAATTAGCCAGGCGTGGTGGTGCATGCCTGTAGTCCCAGCTG CCCGTCTCTACAAAAAAATACATAAATTAGCCGGGCGTGGTGGTGCATGCCTGTAGTCCCAGCTG A G AL513165.1 Ensembl:ENSG00000234160 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1138841 Functional Loss SNV dbSNP153 33..33 33 - - - 10122 RMVar_ID_10122 Human_SNP_ID_397773225 A-to-I Human chr9 + 37510300 37510300 37510300 AGGAGGTCAAGGCTGCGGTGAACCATGATCACACCACTGCACTCTAGCCTGGGCAACAGAGTGAG AGGAGGTCAAGGCTGCGGTGAACCATGATCACGCCACTGCACTCTAGCCTGGGCAACAGAGTGAG A G - - Other Unknown GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1138843 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26224393 Human_Splice_Rec_1044648 10123 RMVar_ID_10123 Human_SNP_ID_397787331 A-to-I Human chr9 - 37568300 37568300 37568300 CCAGCTACCCGAGAAGCTGAGGCAGGAGAATCACTTGAATCCAGGAGGTGGCAGTTGCAGTGAGC CCAGCTACCCGAGAAGCTGAGGCAGGAGAATCGCTTGAATCCAGGAGGTGGCAGTTGCAGTGAGC T C FBXO10,AL513165.2 Ensembl:ENSG00000147912,Ensembl:ENSG00000256966 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1266733597 Functional Loss SNV dbSNP153 33..33 33 - - - 10124 RMVar_ID_10124 Human_SNP_ID_397792456 A-to-I Human chr9 - 37591095 37591095 37591095 GACTTAGCAAGGAAGGAAGGTATCAGAGTTATAGGAACACTGAATATAAGAACTGGAAGCAGCTT GACTTAGCAAGGAAGGAAGGTATCAGAGTTATGGGAACACTGAATATAAGAACTGGAAGCAGCTT T C AL513165.2,AL138752.2,TOMM5 Ensembl:ENSG00000256966,Ensembl:ENSG00000255872,Ensembl:ENSG00000175768 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1478206766 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16680706 RMVar_hsa_circ_5029 10125 RMVar_ID_10125 Human_SNP_ID_397836280 A-to-I Human chr9 + 37769124 37769124 37769124 GAGCTCAGGAGCTCGAGACTAGCCTTGGCAATATGGTGAAACCCCGTCCCTACTAAAAATACGAA GAGCTCAGGAGCTCGAGACTAGCCTTGGCAATCTGGTGAAACCCCGTCCCTACTAAAAATACGAA A C TRMT10B Ensembl:ENSG00000165275 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025853660 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22689948 RMVar_hsa_circ_59879,RMVar_hsa_circ_306122,RMVar_hsa_circ_74047,RMVar_hsa_circ_15441,RMVar_hsa_circ_274945,RMVar_hsa_circ_256935,RMVar_hsa_circ_291818,RMVar_hsa_circ_265227,RMVar_hsa_circ_256937,RMVar_hsa_circ_256938,RMVar_hsa_circ_256936 10126 RMVar_ID_10126 Human_SNP_ID_397836281 A-to-I Human chr9 + 37769124 37769124 37769124 GAGCTCAGGAGCTCGAGACTAGCCTTGGCAATATGGTGAAACCCCGTCCCTACTAAAAATACGAA GAGCTCAGGAGCTCGAGACTAGCCTTGGCAATGTGGTGAAACCCCGTCCCTACTAAAAATACGAA A G TRMT10B Ensembl:ENSG00000165275 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025853660 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22689948 RMVar_hsa_circ_59879,RMVar_hsa_circ_306122,RMVar_hsa_circ_74047,RMVar_hsa_circ_15441,RMVar_hsa_circ_274945,RMVar_hsa_circ_256935,RMVar_hsa_circ_291818,RMVar_hsa_circ_265227,RMVar_hsa_circ_256937,RMVar_hsa_circ_256938,RMVar_hsa_circ_256936 10127 RMVar_ID_10127 Human_SNP_ID_397836313 A-to-I Human chr9 + 37769214 37769214 37769214 CCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGGATCACTTGAGCTTGAGAGGCAGAGGTT CCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCGGGAGGATCACTTGAGCTTGAGAGGCAGAGGTT A G TRMT10B Ensembl:ENSG00000165275 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs755142097 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59879,RMVar_hsa_circ_306122,RMVar_hsa_circ_74047,RMVar_hsa_circ_15441,RMVar_hsa_circ_274945,RMVar_hsa_circ_256935,RMVar_hsa_circ_291818,RMVar_hsa_circ_265227,RMVar_hsa_circ_256937,RMVar_hsa_circ_256938,RMVar_hsa_circ_256936 10128 RMVar_ID_10128 Human_SNP_ID_397837204 A-to-I Human chr9 - 37772080 37772080 37772080 ATGAGCCCATGAGATTGCGGCTGCAGTGAGCCATGATCGCACCACTGCACTCCAGCCTGGGCAAC ATGAGCCCATGAGATTGCGGCTGCAGTGAGCCGTGATCGCACCACTGCACTCCAGCCTGGGCAAC T C AL138752.2,EXOSC3 Ensembl:ENSG00000255872,Ensembl:ENSG00000107371 Protein coding,Protein coding intron,intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs997958520 Functional Loss SNV dbSNP153 33..33 33 - - - 10129 RMVar_ID_10129 Human_SNP_ID_397837239 A-to-I Human chr9 - 37772240 37772240 37772240 GGGAGGCTGAGGTGAGTAGATTGCTTGAGTCCAGGAGTTCAAGACCAGCCTGGAAAACATGGTGA GGGAGGCTGAGGTGAGTAGATTGCTTGAGTCCGGGAGTTCAAGACCAGCCTGGAAAACATGGTGA T C AL138752.2,EXOSC3 Ensembl:ENSG00000255872,Ensembl:ENSG00000107371 Protein coding,Protein coding intron,intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs927391872 Functional Loss SNV dbSNP153 33..33 33 - - - 10130 RMVar_ID_10130 Human_SNP_ID_397837289 A-to-I Human chr9 - 37772424 37772424 37772424 CACGAGGCTGGGCACGGTGGCTCACACCCGTAATCCCAGCAATTTGGGAGGCTGAGGCAGGAGGA CACGAGGCTGGGCACGGTGGCTCACACCCGTATTCCCAGCAATTTGGGAGGCTGAGGCAGGAGGA T A AL138752.2,EXOSC3 Ensembl:ENSG00000255872,Ensembl:ENSG00000107371 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs563728066 Functional Loss SNV dbSNP153 33..33 33 - - - 10131 RMVar_ID_10131 Human_SNP_ID_397837320 A-to-I Human chr9 - 37772556 37772556 37772556 ACATTTTCTGGGCCAGATGAGGACTCATGCCTATAATCCCAGCACTCTGGGATGCTGAGGTAGGA ACATTTTCTGGGCCAGATGAGGACTCATGCCTGTAATCCCAGCACTCTGGGATGCTGAGGTAGGA T C AL138752.2,EXOSC3 Ensembl:ENSG00000255872,Ensembl:ENSG00000107371 Protein coding,Protein coding intron,intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1478459043 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16680865 10132 RMVar_ID_10132 Human_SNP_ID_397837586 A-to-I Human chr9 - 37773668 37773668 37773668 CACCACACTCAGCTAATTTTTATGTTTTTAGTAGAGACAGGGTTTTCACATGTTGGCCAGGATGG CACCACACTCAGCTAATTTTTATGTTTTTAGTGGAGACAGGGTTTTCACATGTTGGCCAGGATGG T C AL138752.2,EXOSC3 Ensembl:ENSG00000255872,Ensembl:ENSG00000107371 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1197614393 Functional Loss SNV dbSNP153 33..33 33 - - - 10133 RMVar_ID_10133 Human_SNP_ID_397838116 A-to-I Human chr9 - 37775605 37775605 37775605 CACTTGAGCCTGGGACATATATCAAGGCTGCAATGAGCTGTGACTGCACCACTGCACTCCAGCCT CACTTGAGCCTGGGACATATATCAAGGCTGCAGTGAGCTGTGACTGCACCACTGCACTCCAGCCT T C AL138752.2,EXOSC3 Ensembl:ENSG00000255872,Ensembl:ENSG00000107371 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1195873461 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16680937 10134 RMVar_ID_10134 Human_SNP_ID_397838902 A-to-I Human chr9 - 37777958 37777958 37777958 CTCTGTCACCCAGGCTGGAGTGCACTGGTGAAATCTCGGCTCACTGCAACCTTCGCCTCCCGAGT CTCTGTCACCCAGGCTGGAGTGCACTGGTGAAGTCTCGGCTCACTGCAACCTTCGCCTCCCGAGT T C AL138752.2,EXOSC3 Ensembl:ENSG00000255872,Ensembl:ENSG00000107371 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs990441326 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16681052,Human_RBP_ID_26224541 10135 RMVar_ID_10135 Human_SNP_ID_397839016 A-to-I Human chr9 - 37778332 37778332 37778332 TTTTGTATTTTTAGTAGAGACGAGGTTTCACCATATTAGCCAGGCTGGTCTGGAACTCCTGACCT TTTTGTATTTTTAGTAGAGACGAGGTTTCACCGTATTAGCCAGGCTGGTCTGGAACTCCTGACCT T C AL138752.2,EXOSC3 Ensembl:ENSG00000255872,Ensembl:ENSG00000107371 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1272722345 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16681069 10136 RMVar_ID_10136 Human_SNP_ID_397863037 A-to-I Human chr9 - 37882879 37882879 37882879 AGATTGCGCCACTGCACTCCAGCCTGGGCAACAGAGTGAAACTCTGTCTCAAAAAAAAAAATTGA AGATTGCGCCACTGCACTCCAGCCTGGGCAACGGAGTGAAACTCTGTCTCAAAAAAAAAAATTGA T C AL138752.2,SLC25A51 Ensembl:ENSG00000255872,Ensembl:ENSG00000122696 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1226343353 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25731,RMVar_hsa_circ_87790,RMVar_hsa_circ_123415,RMVar_hsa_circ_256954,RMVar_hsa_circ_125064,RMVar_hsa_circ_256955,RMVar_hsa_circ_256956 10137 RMVar_ID_10137 Human_SNP_ID_397863697 A-to-I Human chr9 - 37885579 37885579 37885579 GCCAAAAAGAGTGAAACTCACAGTGAAACCCCATCTCTACTAAAAATACAAAAAATTAGCCAGGC GCCAAAAAGAGTGAAACTCACAGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTAGCCAGGC T C AL138752.2,SLC25A51 Ensembl:ENSG00000255872,Ensembl:ENSG00000122696 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1266844802 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_719245 RMVar_hsa_circ_25731,RMVar_hsa_circ_87790,RMVar_hsa_circ_123415,RMVar_hsa_circ_256954,RMVar_hsa_circ_125064,RMVar_hsa_circ_256955,RMVar_hsa_circ_256956 10138 RMVar_ID_10138 Human_SNP_ID_397871518 A-to-I Human chr9 - 37915842 37915842 37915842 CTTTTTTTTTTGAGACAGGGTCTTTCTCTGTTACCCAGCCTGGGGTGCAGTGGCACAGTCTCCAC CTTTTTTTTTTGAGACAGGGTCTTTCTCTGTTTCCCAGCCTGGGGTGCAGTGGCACAGTCTCCAC T A AL138752.2 Ensembl:ENSG00000255872 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1276217142 Functional Loss SNV dbSNP153 33..33 33 - - - 10139 RMVar_ID_10139 Human_SNP_ID_397879537 A-to-I Human chr9 - 37946693 37946693 37946693 TCAGGGAGGACAGGACAGAGCACTCCATGCCAAACCGGGCCGTTCATCCTAGAGGACCAGAGCCC TCAGGGAGGACAGGACAGAGCACTCCATGCCAGACCGGGCCGTTCATCCTAGAGGACCAGAGCCC T C SHB,AL138752.2 Ensembl:ENSG00000107338,Ensembl:ENSG00000255872 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs549307675 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16682546 10140 RMVar_ID_10140 Human_SNP_ID_398026396 A-to-I Human chr9 - 38544537 38544537 38544537 CAGCCCTCGCAGGGTCTGACCTCCCAGCATGCACCTGCCCCTCCCTGCACCCCAGATGTCCACCC CAGCCCTCGCAGGGTCTGACCTCCCAGCATGCTCCTGCCCCTCCCTGCACCCCAGATGTCCACCC T A AL390726.2,FAM95C Ensembl:ENSG00000272904,Ensembl:ENSG00000283486 lincRNA,Protein coding intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1000000570 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105053,RMVar_hsa_circ_256973 10141 RMVar_ID_10141 Human_SNP_ID_398026397 A-to-I Human chr9 - 38544537 38544537 38544537 CAGCCCTCGCAGGGTCTGACCTCCCAGCATGCACCTGCCCCTCCCTGCACCCCAGATGTCCACCC CAGCCCTCGCAGGGTCTGACCTCCCAGCATGCGCCTGCCCCTCCCTGCACCCCAGATGTCCACCC T C AL390726.2,FAM95C Ensembl:ENSG00000272904,Ensembl:ENSG00000283486 lincRNA,Protein coding intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1000000570 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105053,RMVar_hsa_circ_256973 10142 RMVar_ID_10142 Human_SNP_ID_398026462 A-to-I Human chr9 - 38544720 38544720 38544720 GTCTCAGACTGCAGAAATTCCAGTCCTGAGATAGGACGGTGCTGCCCAGGGTGGGTGGCCAGGGC GTCTCAGACTGCAGAAATTCCAGTCCTGAGATGGGACGGTGCTGCCCAGGGTGGGTGGCCAGGGC T C AL390726.2,FAM95C Ensembl:ENSG00000272904,Ensembl:ENSG00000283486 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432248336 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105053,RMVar_hsa_circ_256973 10143 RMVar_ID_10143 Human_SNP_ID_398026464 A-to-I Human chr9 - 38544724 38544724 38544724 TCCTGTCTCAGACTGCAGAAATTCCAGTCCTGAGATAGGACGGTGCTGCCCAGGGTGGGTGGCCA TCCTGTCTCAGACTGCAGAAATTCCAGTCCTGGGATAGGACGGTGCTGCCCAGGGTGGGTGGCCA T C AL390726.2,FAM95C Ensembl:ENSG00000272904,Ensembl:ENSG00000283486 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1173573300 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105053,RMVar_hsa_circ_256973 10144 RMVar_ID_10144 Human_SNP_ID_398026588 A-to-I Human chr9 - 38545227 38545227 38545227 GTGATGTGGTCACTCCCTGGGGGACTGCTGTCAGGCACCGGGCACCCACCATGGGCAGCACTGTC GTGATGTGGTCACTCCCTGGGGGACTGCTGTCGGGCACCGGGCACCCACCATGGGCAGCACTGTC T C AL390726.2,FAM95C Ensembl:ENSG00000272904,Ensembl:ENSG00000283486 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1475044781 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105053,RMVar_hsa_circ_256973 10145 RMVar_ID_10145 Human_SNP_ID_398027676 A-to-I Human chr9 - 38549400 38549400 38549400 GGAGTCAGTACTCAGCTTCTTTTCATTCAAGTATCTGAGGGCTTCTTGAATTTTCTCCCTGAAAA GGAGTCAGTACTCAGCTTCTTTTCATTCAAGTCTCTGAGGGCTTCTTGAATTTTCTCCCTGAAAA T G AL390726.2,FAM95C Ensembl:ENSG00000272904,Ensembl:ENSG00000283486 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs556619926 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5029588,Human_RBP_ID_17579273,Human_RBP_ID_26224808 RMVar_hsa_circ_105053,RMVar_hsa_circ_256973 10146 RMVar_ID_10146 Human_SNP_ID_398027694 A-to-I Human chr9 - 38549463 38549463 38549463 AGAAAATTAGTACTGGGAAGTGGATGTATGAAATGTCTTCAAGGCCTTTTCCCTATTGTCTTGGG AGAAAATTAGTACTGGGAAGTGGATGTATGAAGTGTCTTCAAGGCCTTTTCCCTATTGTCTTGGG T C AL390726.2,FAM95C Ensembl:ENSG00000272904,Ensembl:ENSG00000283486 lincRNA,Protein coding intron,intron GSE100210;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229 RNA-Seq:(High) rs940551525 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17579273 RMVar_hsa_circ_105053,RMVar_hsa_circ_256973 10147 RMVar_ID_10147 Human_SNP_ID_398028948 A-to-I Human chr9 - 38554468 38554468 38554468 ATACGGTGGGAGCCCCCACACTGGGAGGCACCATTCTCCAGACCCCAGATTCATAGACCCACCAA ATACGGTGGGAGCCCCCACACTGGGAGGCACCGTTCTCCAGACCCCAGATTCATAGACCCACCAA T C AL390726.2,FAM95C Ensembl:ENSG00000272904,Ensembl:ENSG00000283486 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1321192985 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2792600 RMVar_hsa_circ_105053,RMVar_hsa_circ_256973 10148 RMVar_ID_10148 Human_SNP_ID_398028950 A-to-I Human chr9 - 38554475 38554475 38554475 GGAACATATACGGTGGGAGCCCCCACACTGGGAGGCACCATTCTCCAGACCCCAGATTCATAGAC GGAACATATACGGTGGGAGCCCCCACACTGGGTGGCACCATTCTCCAGACCCCAGATTCATAGAC T A AL390726.2,FAM95C Ensembl:ENSG00000272904,Ensembl:ENSG00000283486 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1163582639 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2792600 RMVar_hsa_circ_105053,RMVar_hsa_circ_256973 10149 RMVar_ID_10149 Human_SNP_ID_398029780 A-to-I Human chr9 - 38557538 38557538 38557538 TGGAGCCCCCATACAGGGAGGCGCCATTTTCCAGACCCCAGATTCATAGACCCACCAACAGCTTG TGGAGCCCCCATACAGGGAGGCGCCATTTTCCGGACCCCAGATTCATAGACCCACCAACAGCTTG T C AL390726.2,FAM95C Ensembl:ENSG00000272904,Ensembl:ENSG00000283486 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1235154667 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3215246 RMVar_hsa_circ_105053,RMVar_hsa_circ_256973 10150 RMVar_ID_10150 Human_SNP_ID_398030027 A-to-I Human chr9 - 38558678 38558678 38558678 AAGCTATGAAATGCCTTCAAGGCCTTTTCCCCAATCTTTTGGCTGGTAGCACTGGGCTTCTTTGA AAGCTATGAAATGCCTTCAAGGCCTTTTCCCCGATCTTTTGGCTGGTAGCACTGGGCTTCTTTGA T C AL390726.2,FAM95C Ensembl:ENSG00000272904,Ensembl:ENSG00000283486 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1026611336 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105053,RMVar_hsa_circ_256973 10151 RMVar_ID_10151 Human_SNP_ID_398030029 A-to-I Human chr9 - 38558692 38558692 38558692 AATGCTGTGAAGTGAAGCTATGAAATGCCTTCAAGGCCTTTTCCCCAATCTTTTGGCTGGTAGCA AATGCTGTGAAGTGAAGCTATGAAATGCCTTCGAGGCCTTTTCCCCAATCTTTTGGCTGGTAGCA T C AL390726.2,FAM95C Ensembl:ENSG00000272904,Ensembl:ENSG00000283486 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1183619388 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105053,RMVar_hsa_circ_256973 10152 RMVar_ID_10152 Human_SNP_ID_398030804 A-to-I Human chr9 - 38561752 38561752 38561752 TTCAATGACTTTTCCCCATCACATTGGCTATTAATACTGGTCTTCCTTTTAGTGCAAATATCTGA TTCAATGACTTTTCCCCATCACATTGGCTATTTATACTGGTCTTCCTTTTAGTGCAAATATCTGA T A AL390726.2,FAM95C Ensembl:ENSG00000272904,Ensembl:ENSG00000283486 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs180795735 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105053,RMVar_hsa_circ_256973 10153 RMVar_ID_10153 Human_SNP_ID_398031430 A-to-I Human chr9 - 38564250 38564250 38564250 TGAAAAATTTGCAGCCTAGCCAAGTGGTCAAAAAGGAAAGCTGATTTTCAGGGGGAAAATTCAAG TGAAAAATTTGCAGCCTAGCCAAGTGGTCAAATAGGAAAGCTGATTTTCAGGGGGAAAATTCAAG T A AL390726.2,FAM95C Ensembl:ENSG00000272904,Ensembl:ENSG00000283486 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1472240608 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2452167 RMVar_hsa_circ_105053,RMVar_hsa_circ_256973 10154 RMVar_ID_10154 Human_SNP_ID_398031584 A-to-I Human chr9 - 38564825 38564825 38564825 GAGCTATGAAATGCCTTCAAGGCCTTTTCCCCATTGTGTTGGTAACCAGTACTCAGCTGCTTTTC GAGCTATGAAATGCCTTCAAGGCCTTTTCCCCGTTGTGTTGGTAACCAGTACTCAGCTGCTTTTC T C AL390726.2,FAM95C Ensembl:ENSG00000272904,Ensembl:ENSG00000283486 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444318206 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105053,RMVar_hsa_circ_256973 10155 RMVar_ID_10155 Human_SNP_ID_398171232 A-to-I Human chr9 - 39137589 39137589 39137589 AGAATGGCATGAATCCGGGAGGCGGAGCATGCAGTGAGCTGAGATCATGCCACTGAACTCCAGCC AGAATGGCATGAATCCGGGAGGCGGAGCATGCCGTGAGCTGAGATCATGCCACTGAACTCCAGCC T G CNTNAP3 Ensembl:ENSG00000106714 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs756522813 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77319,RMVar_hsa_circ_256975,RMVar_hsa_circ_256979,RMVar_hsa_circ_82187,RMVar_hsa_circ_39977,RMVar_hsa_circ_293931,RMVar_hsa_circ_316802 10156 RMVar_ID_10156 Human_SNP_ID_398179940 A-to-I Human chr9 - 39175269 39175267 39175269 TGGTCTCGATCTCCCAACCTCGTGATCTGCCCACCTCGGCCTCCCAAAGTGCTAGGACCACAGGC TGGTCTCGATCTCCCAACCTCGTGATCTGCCC__CTCGGCCTCCCAAAGTGCTAGGACCACAGGC GGT G CNTNAP3 Ensembl:ENSG00000106714 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs943938070 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_256979,RMVar_hsa_circ_82187,RMVar_hsa_circ_316802,RMVar_hsa_circ_256984,RMVar_hsa_circ_286322,RMVar_hsa_circ_326761 10157 RMVar_ID_10157 Human_SNP_ID_398179941 A-to-I Human chr9 - 39175269 39175269 39175269 TGGTCTCGATCTCCCAACCTCGTGATCTGCCCACCTCGGCCTCCCAAAGTGCTAGGACCACAGGC TGGTCTCGATCTCCCAACCTCGTGATCTGCCCGCCTCGGCCTCCCAAAGTGCTAGGACCACAGGC T C CNTNAP3 Ensembl:ENSG00000106714 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1280998615 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_256979,RMVar_hsa_circ_82187,RMVar_hsa_circ_316802,RMVar_hsa_circ_256984,RMVar_hsa_circ_286322,RMVar_hsa_circ_326761 10158 RMVar_ID_10158 Human_SNP_ID_398314546 A-to-I Human chr9 - 40092033 40092033 40092033 GAGTAGCTGGGATTACAGCCACATGCCACCACACCCAGCTAATGTTTGTATTTTTAGTAGATACG GAGTAGCTGGGATTACAGCCACATGCCACCACGCCCAGCTAATGTTTGTATTTTTAGTAGATACG T C FGF7P3,AL772307.1 Ensembl:ENSG00000204837,Ensembl:ENSG00000284116 Pseudogene,lincRNA intron,intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1412079837 Functional Loss SNV dbSNP153 33..33 33 - - - 10159 RMVar_ID_10159 Human_SNP_ID_398349359 A-to-I Human chr9 + 40325426 40325426 40325426 CTGGGAAGTGCTTCCAGGGTTTCATATGTGTTATGGAGATGCTTCCTCTCTCCAACCTCACCGTG CTGGGAAGTGCTTCCAGGGTTTCATATGTGTTGTGGAGATGCTTCCTCTCTCCAACCTCACCGTG A G BX664727.3,FAM95B1 Ensembl:ENSG00000240240,Ensembl:ENSG00000223839 lincRNA,Pseudogene intron,intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs4925947 Functional Loss SNV dbSNP153 33..33 33 - - - 10160 RMVar_ID_10160 Human_SNP_ID_398349566 A-to-I Human chr9 + 40326321 40326321 40326321 AGACCCAAGCCTGCCTTGCTGCCACTTAGGATATGACAGCACAGCCAGTGGCCTCTACTGGATCC AGACCCAAGCCTGCCTTGCTGCCACTTAGGATGTGACAGCACAGCCAGTGGCCTCTACTGGATCC A G BX664727.3,FAM95B1 Ensembl:ENSG00000240240,Ensembl:ENSG00000223839 lincRNA,Pseudogene intron,exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1284795417 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1045800,Human_Splice_Rec_1045838,Human_Splice_Rec_1045844,Human_Splice_Rec_1045848,Human_Splice_Rec_1045852,Human_Splice_Rec_1045858 10161 RMVar_ID_10161 Human_SNP_ID_398559130 A-to-I Human chr9 - 41037331 41037331 41037331 GCAATCCTCCCAACTCAGCCTCCTGAGTAGCTAGGACTACACATGCGCCATCATACCCAGTTAAT GCAATCCTCCCAACTCAGCCTCCTGAGTAGCTTGGACTACACATGCGCCATCATACCCAGTTAAT T A PGM5P2 Ensembl:ENSG00000277778 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1210158565 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_309875 10162 RMVar_ID_10162 Human_SNP_ID_398559132 A-to-I Human chr9 - 41037335 41037335 41037335 TCAAGCAATCCTCCCAACTCAGCCTCCTGAGTAGCTAGGACTACACATGCGCCATCATACCCAGT TCAAGCAATCCTCCCAACTCAGCCTCCTGAGTGGCTAGGACTACACATGCGCCATCATACCCAGT T C PGM5P2 Ensembl:ENSG00000277778 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1263865082 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_309875 10163 RMVar_ID_10163 Human_SNP_ID_398559134 A-to-I Human chr9 - 41037352 41037340 41037353 ACCTTCAACTGCTGGGCTCAAGCAATCCTCCCAACTCAGCCTCCTGAGTAGCTAGGACTACACAT ACCTTCAACTGCTGGGCTCAAGCAATCCTCC_____________TGAGTAGCTAGGACTACACAT AGGAGGCTGAGTTG A PGM5P2 Ensembl:ENSG00000277778 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1354746398 Functional Loss DEL dbSNP153 32..44 33 - - - RMVar_hsa_circ_309875 10164 RMVar_ID_10164 Human_SNP_ID_398559139 A-to-I Human chr9 - 41037351 41037351 41037351 CCTTCAACTGCTGGGCTCAAGCAATCCTCCCAACTCAGCCTCCTGAGTAGCTAGGACTACACATG CCTTCAACTGCTGGGCTCAAGCAATCCTCCCACCTCAGCCTCCTGAGTAGCTAGGACTACACATG T G PGM5P2 Ensembl:ENSG00000277778 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1386496413 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_309875 10165 RMVar_ID_10165 Human_SNP_ID_642678736 A-to-I Human chr18 - 31833880 31833880 31833880 CTTCTGCCTCAGCCTCCCGAGTAACTGGGACTATAGGCACCTGCCACCACGCCCGGCTACTTTTT CTTCTGCCTCAGCCTCCCGAGTAACTGGGACTGTAGGCACCTGCCACCACGCCCGGCTACTTTTT T C TRAPPC8 Ensembl:ENSG00000153339 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1188633881 Functional Loss SNV dbSNP153 33..33 33 - - - 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 10166 RMVar_ID_10166 Human_SNP_ID_642679335 A-to-I Human chr18 - 31836313 31836313 31836313 AAGAGTGGGTTAAATGAAGCATTCCAAAATCAAAACTCTGCATGGAAGTATGTGAAAACAAGGCA AAGAGTGGGTTAAATGAAGCATTCCAAAATCAGAACTCTGCATGGAAGTATGTGAAAACAAGGCA T C TRAPPC8 Ensembl:ENSG00000153339 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1487696785 Functional Loss SNV dbSNP153 33..33 33 - - - 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 10167 RMVar_ID_10167 Human_SNP_ID_642679338 A-to-I Human chr18 - 31836317 31836317 31836317 GTAGAAGAGTGGGTTAAATGAAGCATTCCAAAATCAAAACTCTGCATGGAAGTATGTGAAAACAA GTAGAAGAGTGGGTTAAATGAAGCATTCCAAAGTCAAAACTCTGCATGGAAGTATGTGAAAACAA T C TRAPPC8 Ensembl:ENSG00000153339 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1000068587 Functional Loss SNV dbSNP153 33..33 33 - - - 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 10168 RMVar_ID_10168 Human_SNP_ID_642679343 A-to-I Human chr18 - 31836352 31836352 31836352 TCTATGTGAAACAGGAAAGTTTTGATCAAACTAAAGTAGAAGAGTGGGTTAAATGAAGCATTCCA TCTATGTGAAACAGGAAAGTTTTGATCAAACTGAAGTAGAAGAGTGGGTTAAATGAAGCATTCCA T C TRAPPC8 Ensembl:ENSG00000153339 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1259702099 Functional Loss SNV dbSNP153 33..33 33 - - - 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 10169 RMVar_ID_10169 Human_SNP_ID_642679349 A-to-I Human chr18 - 31836374 31836374 31836374 GGGGTTAAAAAACCCTATGGAATCTATGTGAAACAGGAAAGTTTTGATCAAACTAAAGTAGAAGA GGGGTTAAAAAACCCTATGGAATCTATGTGAAGCAGGAAAGTTTTGATCAAACTAAAGTAGAAGA T C TRAPPC8 Ensembl:ENSG00000153339 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1446005677 Functional Loss SNV dbSNP153 33..33 33 - - - 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 10170 RMVar_ID_10170 Human_SNP_ID_642707512 A-to-I Human chr18 - 31937800 31937800 31937800 GCTCGGGAGGCTGAGGCAGGAGAATCACTTGAACTCGAGAGGTGAAGGTTGCAGTGAGCCAAGAT GCTCGGGAGGCTGAGGCAGGAGAATCACTTGAGCTCGAGAGGTGAAGGTTGCAGTGAGCCAAGAT T C TRAPPC8 Ensembl:ENSG00000153339 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1332470009 Functional Loss SNV dbSNP153 33..33 33 - - - 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 10171 RMVar_ID_10171 Human_SNP_ID_642714779 A-to-I Human chr18 - 31962477 31962477 31962477 CTTGTGGTGTCCCTATATTCAGAATTTCCTCCATCAATGATGATGTCACCAATGTCCAACAATGG CTTGTGGTGTCCCTATATTCAGAATTTCCTCCGTCAATGATGATGTCACCAATGTCCAACAATGG T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs878944841 Functional Loss SNV dbSNP153 33..33 33 - - - 10172 RMVar_ID_10172 Human_SNP_ID_642714837 A-to-I Human chr18 - 31962654 31962654 31962654 AGTCACAGCAGGGTTCCTACTTTTGCAGCAACACCTTGGAAGATGGTCTTGATGTGGGGCCATGC AGTCACAGCAGGGTTCCTACTTTTGCAGCAACGCCTTGGAAGATGGTCTTGATGTGGGGCCATGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1296906526 Functional Loss SNV dbSNP153 33..33 33 - - - 10173 RMVar_ID_10173 Human_SNP_ID_642714983 A-to-I Human chr18 - 31963244 31963244 31963244 CTAATAATGCAGCCCCCTCTCCACATCAGGGCAATATCACCATAATTGAGGGTCCAGCCAAACTC CTAATAATGCAGCCCCCTCTCCACATCAGGGCGATATCACCATAATTGAGGGTCCAGCCAAACTC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1253589539 Functional Loss SNV dbSNP153 33..33 33 - - - 10174 RMVar_ID_10174 Human_SNP_ID_642714993 A-to-I Human chr18 - 31963271 31963271 31963271 TCCTTTATCTTTCCTAGGAATACACTTCTAATAATGCAGCCCCCTCTCCACATCAGGGCAATATC TCCTTTATCTTTCCTAGGAATACACTTCTAATGATGCAGCCCCCTCTCCACATCAGGGCAATATC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879108054 Functional Loss SNV dbSNP153 33..33 33 - - - 10175 RMVar_ID_10175 Human_SNP_ID_642733757 A-to-I Human chr18 + 32039000 32039000 32039000 GTTGGCCAGTCTGGTCTTGAACTCCTGACCTCAGGCGATCTGCCCGCCTCGGACTCCCAAAGTGC GTTGGCCAGTCTGGTCTTGAACTCCTGACCTCGGGCGATCTGCCCGCCTCGGACTCCCAAAGTGC A G AC011825.3,RNF125 Ensembl:ENSG00000263917,Ensembl:ENSG00000101695 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1488339696 Functional Loss SNV dbSNP153 33..33 33 - - - 10176 RMVar_ID_10176 Human_SNP_ID_642741207 A-to-I Human chr18 + 32068963 32068963 32068963 TACGCTTGTAATCCCAGCACTTTGGGAGGCTGAAGCAGGCGGATCACAAGGTCAGGAGTTCGAGA TACGCTTGTAATCCCAGCACTTTGGGAGGCTGCAGCAGGCGGATCACAAGGTCAGGAGTTCGAGA A C AC011825.3,RNF125 Ensembl:ENSG00000263917,Ensembl:ENSG00000101695 lincRNA,Protein coding intron,3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1383629828 Functional Loss SNV dbSNP153 33..33 33 - - - 10177 RMVar_ID_10177 Human_SNP_ID_642741228 A-to-I Human chr18 + 32069036 32069036 32069036 GCCAACACTGGTCTCTGTGAAACTCCGTCTCTACTAAAAATACAAAAATTAGCTGGACGTGTTGG GCCAACACTGGTCTCTGTGAAACTCCGTCTCTGCTAAAAATACAAAAATTAGCTGGACGTGTTGG A G AC011825.3,RNF125 Ensembl:ENSG00000263917,Ensembl:ENSG00000101695 lincRNA,Protein coding intron,3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1325306286 Functional Loss SNV dbSNP153 33..33 33 - - - 10178 RMVar_ID_10178 Human_SNP_ID_642741229 A-to-I Human chr18 + 32069036 32069036 32069036 GCCAACACTGGTCTCTGTGAAACTCCGTCTCTACTAAAAATACAAAAATTAGCTGGACGTGTTGG GCCAACACTGGTCTCTGTGAAACTCCGTCTCTTCTAAAAATACAAAAATTAGCTGGACGTGTTGG A T AC011825.3,RNF125 Ensembl:ENSG00000263917,Ensembl:ENSG00000101695 lincRNA,Protein coding intron,3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1325306286 Functional Loss SNV dbSNP153 33..33 33 - - - 10179 RMVar_ID_10179 Human_SNP_ID_642741238 A-to-I Human chr18 + 32069080 32069080 32069080 AAAATTAGCTGGACGTGTTGGCGGGCATCTGTAATACCAGCTACTTGGGAGGCTGAGGCAGAAGA AAAATTAGCTGGACGTGTTGGCGGGCATCTGTGATACCAGCTACTTGGGAGGCTGAGGCAGAAGA A G AC011825.3,RNF125 Ensembl:ENSG00000263917,Ensembl:ENSG00000101695 lincRNA,Protein coding intron,3'UTR GSE47997;GSE38233;GSE38233;GSE100210;GSE100210 K562 cells&HepG2 cells;cultured B-cells;cultured B-cells;HepG2 cell line;HepG2 cell line - 23474544,24183664,24183664,29129909,29129909 RNA-Seq:(High) rs1184331182 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1741996 10180 RMVar_ID_10180 Human_SNP_ID_642741240 A-to-I Human chr18 + 32069090 32069090 32069090 GGACGTGTTGGCGGGCATCTGTAATACCAGCTACTTGGGAGGCTGAGGCAGAAGAATCACTTGAA GGACGTGTTGGCGGGCATCTGTAATACCAGCTTCTTGGGAGGCTGAGGCAGAAGAATCACTTGAA A T AC011825.3,RNF125 Ensembl:ENSG00000263917,Ensembl:ENSG00000101695 lincRNA,Protein coding intron,3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs920700165 Functional Loss SNV dbSNP153 33..33 33 - - - 10181 RMVar_ID_10181 Human_SNP_ID_642741246 A-to-I Human chr18 + 32069109 32069109 32069109 TGTAATACCAGCTACTTGGGAGGCTGAGGCAGAAGAATCACTTGAACCCGGGAGGCAGAGGTTAC TGTAATACCAGCTACTTGGGAGGCTGAGGCAGGAGAATCACTTGAACCCGGGAGGCAGAGGTTAC A G AC011825.3,RNF125 Ensembl:ENSG00000263917,Ensembl:ENSG00000101695 lincRNA,Protein coding intron,3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1315136223 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_196732,Human_miRNA_ID_697405,Human_miRNA_ID_702339,Human_miRNA_ID_1462360 10182 RMVar_ID_10182 Human_SNP_ID_642741248 A-to-I Human chr18 + 32069121 32069121 32069121 TACTTGGGAGGCTGAGGCAGAAGAATCACTTGAACCCGGGAGGCAGAGGTTACAGTGAGCTGAGA TACTTGGGAGGCTGAGGCAGAAGAATCACTTGGACCCGGGAGGCAGAGGTTACAGTGAGCTGAGA A G AC011825.3,RNF125 Ensembl:ENSG00000263917,Ensembl:ENSG00000101695 lincRNA,Protein coding intron,3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1379960855 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_196732,Human_miRNA_ID_697405,Human_miRNA_ID_702339,Human_miRNA_ID_1462360 10183 RMVar_ID_10183 Human_SNP_ID_642741252 A-to-I Human chr18 + 32069129 32069129 32069129 AGGCTGAGGCAGAAGAATCACTTGAACCCGGGAGGCAGAGGTTACAGTGAGCTGAGATCGCACCA AGGCTGAGGCAGAAGAATCACTTGAACCCGGGGGGCAGAGGTTACAGTGAGCTGAGATCGCACCA A G AC011825.3,RNF125 Ensembl:ENSG00000263917,Ensembl:ENSG00000101695 lincRNA,Protein coding intron,3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1168116095 Functional Loss SNV dbSNP153 33..33 33 - - - 10184 RMVar_ID_10184 Human_SNP_ID_642741259 A-to-I Human chr18 + 32069158 32069158 32069158 GGGAGGCAGAGGTTACAGTGAGCTGAGATCGCACCAGTACACTCCAGCCTGGGTAACAGAGCTAG GGGAGGCAGAGGTTACAGTGAGCTGAGATCGCTCCAGTACACTCCAGCCTGGGTAACAGAGCTAG A T AC011825.3,RNF125 Ensembl:ENSG00000263917,Ensembl:ENSG00000101695 lincRNA,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1183174408 Functional Loss SNV dbSNP153 33..33 33 - - - 10185 RMVar_ID_10185 Human_SNP_ID_642741473 A-to-I Human chr18 + 32070102 32070102 32070102 GCACTCTGTTGCCCAGGCTGGAGTACAGTGGCACGATCTCGACTCACTGCAACCTCCATCTCCCG GCACTCTGTTGCCCAGGCTGGAGTACAGTGGCGCGATCTCGACTCACTGCAACCTCCATCTCCCG A G AC011825.3,RNF125 Ensembl:ENSG00000263917,Ensembl:ENSG00000101695 lincRNA,Protein coding intron,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs542865235 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_44 GWAS_ID_971,GWAS_ID_972,GWAS_ID_973 10186 RMVar_ID_10186 Human_SNP_ID_642741513 A-to-I Human chr18 + 32070221 32070221 32070221 CGCCACCATGCCCGGCTAATTTTTGTATTTTTAGTAGAGGGGTTTCACCATAATGGTCAGGCTGG CGCCACCATGCCCGGCTAATTTTTGTATTTTTGGTAGAGGGGTTTCACCATAATGGTCAGGCTGG A G AC011825.3,RNF125 Ensembl:ENSG00000263917,Ensembl:ENSG00000101695 lincRNA,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1010437482 Functional Loss SNV dbSNP153 33..33 33 - - - 10187 RMVar_ID_10187 Human_SNP_ID_642741660 A-to-I Human chr18 + 32070808 32070808 32070808 CTCACTGCAACCTCTGCCTCCTGGATTCAAGCAATTCTCCTGCCTCAGCTTCCCGAGTAGCTGGG CTCACTGCAACCTCTGCCTCCTGGATTCAAGCGATTCTCCTGCCTCAGCTTCCCGAGTAGCTGGG A G AC011825.3,RNF125 Ensembl:ENSG00000263917,Ensembl:ENSG00000101695 lincRNA,Protein coding intron,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1025960814 Functional Loss SNV dbSNP153 33..33 33 - - - 10188 RMVar_ID_10188 Human_SNP_ID_642741677 A-to-I Human chr18 + 32070884 32070875 32070884 GCGCCACCACGCCCTGCTAATTTTGTATTTTTAGTAGAGTCAGGATTTCTCCACATTGGTCAGGC GCGCCACCACGCCCTGCTAATTTT_________GTAGAGTCAGGATTTCTCCACATTGGTCAGGC TGTATTTTTA T AC011825.3,RNF125 Ensembl:ENSG00000263917,Ensembl:ENSG00000101695 lincRNA,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444501232 Functional Loss DEL dbSNP153 25..33 33 - - - 10189 RMVar_ID_10189 Human_SNP_ID_642741766 A-to-I Human chr18 + 32071276 32071276 32071276 CCTGCCTCAGCCTCTCGAGTAGCTGGGATTACAAGTGGGCACCACCACACCCGGCTAATTGTTGT CCTGCCTCAGCCTCTCGAGTAGCTGGGATTACGAGTGGGCACCACCACACCCGGCTAATTGTTGT A G AC011825.3,RNF125 Ensembl:ENSG00000263917,Ensembl:ENSG00000101695 lincRNA,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1055481414 Functional Loss SNV dbSNP153 33..33 33 - - - 10190 RMVar_ID_10190 Human_SNP_ID_642741801 A-to-I Human chr18 + 32071408 32071408 32071408 CACCTGTGTTGGCCTCCTAAAGTACTGGGATTACAGGTGTGTGCCACCGCGCCAGGCAATTGCCC CACCTGTGTTGGCCTCCTAAAGTACTGGGATTCCAGGTGTGTGCCACCGCGCCAGGCAATTGCCC A C AC011825.3,RNF125 Ensembl:ENSG00000263917,Ensembl:ENSG00000101695 lincRNA,Protein coding intron,3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1213940709 Functional Loss SNV dbSNP153 33..33 33 - - - 10191 RMVar_ID_10191 Human_SNP_ID_642741903 A-to-I Human chr18 + 32071927 32071927 32071927 CAAAATCTGGCTGGTTACAGTGGCTCACACCTATAATCCCAGCACTTTGGGAGGCTGAGGTGGAG CAAAATCTGGCTGGTTACAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGAG A G AC011825.3,RNF125 Ensembl:ENSG00000263917,Ensembl:ENSG00000101695 lincRNA,Protein coding intron,3'UTR GSE47997;GSE38233;GSE38233 K562 cells&HepG2 cells;cultured B-cells;cultured B-cells - 23474544,24183664,24183664 RNA-Seq:(High) rs1459733956 Functional Loss SNV dbSNP153 33..33 33 - - - 10192 RMVar_ID_10192 Human_SNP_ID_642741938 A-to-I Human chr18 + 32072080 32072080 32072080 CAAACAAAAAGCTGGGCATGATGCACACCTTTAGTTTCAGCTACTAAGGAGGCTGAGGTTGGAGG CAAACAAAAAGCTGGGCATGATGCACACCTTTGGTTTCAGCTACTAAGGAGGCTGAGGTTGGAGG A G AC011825.3,RNF125 Ensembl:ENSG00000263917,Ensembl:ENSG00000101695 lincRNA,Protein coding intron,3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs879225873 Functional Loss SNV dbSNP153 33..33 33 - - - 10193 RMVar_ID_10193 Human_SNP_ID_642750317 A-to-I Human chr18 + 32104033 32104032 32104033 TAGGCTAAAAAACTTTTTTTTTTTTTTTTTGGAGGCAGAGTCTAGTTCTGTCGCCCATGCCAGAG TAGGCTAAAAAACTTTTTTTTTTTTTTTTTGG_GGCAGAGTCTAGTTCTGTCGCCCATGCCAGAG GA G RNF138,AC011825.3 Ensembl:ENSG00000134758,Ensembl:ENSG00000263917 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1412804073 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_7147,Human_RBP_ID_13283964 10194 RMVar_ID_10194 Human_SNP_ID_642750318 A-to-I Human chr18 + 32104033 32104033 32104033 TAGGCTAAAAAACTTTTTTTTTTTTTTTTTGGAGGCAGAGTCTAGTTCTGTCGCCCATGCCAGAG TAGGCTAAAAAACTTTTTTTTTTTTTTTTTGGGGGCAGAGTCTAGTTCTGTCGCCCATGCCAGAG A G RNF138,AC011825.3 Ensembl:ENSG00000134758,Ensembl:ENSG00000263917 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992802182 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7147,Human_RBP_ID_13283964 10195 RMVar_ID_10195 Human_SNP_ID_642750319 A-to-I Human chr18 + 32104033 32104033 32104033 TAGGCTAAAAAACTTTTTTTTTTTTTTTTTGGAGGCAGAGTCTAGTTCTGTCGCCCATGCCAGAG TAGGCTAAAAAACTTTTTTTTTTTTTTTTTGGTGGCAGAGTCTAGTTCTGTCGCCCATGCCAGAG A T RNF138,AC011825.3 Ensembl:ENSG00000134758,Ensembl:ENSG00000263917 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992802182 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7147,Human_RBP_ID_13283964 10196 RMVar_ID_10196 Human_SNP_ID_642754361 A-to-I Human chr18 + 32120051 32120051 32120051 GTTTTGTCTGCTTCTTTTAAACCTAATGTTCTATATAATACTTGATTTATTGCATTGAATAGGTT GTTTTGTCTGCTTCTTTTAAACCTAATGTTCTGTATAATACTTGATTTATTGCATTGAATAGGTT A G RNF138 Ensembl:ENSG00000134758 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs955546944 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_31166,RMVar_hsa_circ_189493,RMVar_hsa_circ_298070,RMVar_hsa_circ_369840,RMVar_hsa_circ_303186,RMVar_hsa_circ_189495,RMVar_hsa_circ_189494,RMVar_hsa_circ_310815,RMVar_hsa_circ_324500,RMVar_hsa_circ_189496 10197 RMVar_ID_10197 Human_SNP_ID_642754436 A-to-I Human chr18 + 32120414 32120414 32120414 ATTTAACATTGGATAGAGATCCTATTGAATGCAGTAAACCAAGTGTGATATAGAACATTAAATTA ATTTAACATTGGATAGAGATCCTATTGAATGCGGTAAACCAAGTGTGATATAGAACATTAAATTA A G RNF138 Ensembl:ENSG00000134758 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs538413182 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17908552 RMVar_hsa_circ_31166,RMVar_hsa_circ_189493,RMVar_hsa_circ_298070,RMVar_hsa_circ_369840,RMVar_hsa_circ_303186,RMVar_hsa_circ_189495,RMVar_hsa_circ_189494,RMVar_hsa_circ_310815,RMVar_hsa_circ_324500,RMVar_hsa_circ_189496 10198 RMVar_ID_10198 Human_SNP_ID_642754437 A-to-I Human chr18 + 32120422 32120422 32120422 TTGGATAGAGATCCTATTGAATGCAGTAAACCAAGTGTGATATAGAACATTAAATTAAAAAGCAA TTGGATAGAGATCCTATTGAATGCAGTAAACCCAGTGTGATATAGAACATTAAATTAAAAAGCAA A C RNF138 Ensembl:ENSG00000134758 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388838113 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17908552 RMVar_hsa_circ_31166,RMVar_hsa_circ_189493,RMVar_hsa_circ_298070,RMVar_hsa_circ_369840,RMVar_hsa_circ_303186,RMVar_hsa_circ_189495,RMVar_hsa_circ_189494,RMVar_hsa_circ_310815,RMVar_hsa_circ_324500,RMVar_hsa_circ_189496 10199 RMVar_ID_10199 Human_SNP_ID_642754547 A-to-I Human chr18 + 32120974 32120973 32120974 CTGGGCCAACATGGTGAAACCCTGTCTCTACTAAAAATACAAAAATTAGCCAGGCATGGTGGCAT CTGGGCCAACATGGTGAAACCCTGTCTCTACT_AAAATACAAAAATTAGCCAGGCATGGTGGCAT TA T RNF138 Ensembl:ENSG00000134758 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1238910681 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_31166,RMVar_hsa_circ_189493,RMVar_hsa_circ_298070,RMVar_hsa_circ_369840,RMVar_hsa_circ_303186,RMVar_hsa_circ_189495,RMVar_hsa_circ_189494,RMVar_hsa_circ_310815,RMVar_hsa_circ_324500,RMVar_hsa_circ_189496 10200 RMVar_ID_10200 Human_SNP_ID_642754811 A-to-I Human chr18 + 32121938 32121938 32121938 TTGCCCAGGCTGGAGTGCAGTGGCATGATCTTAGCTCACTGCAACCTCCGCCTTCCGGTTTCAAG TTGCCCAGGCTGGAGTGCAGTGGCATGATCTTGGCTCACTGCAACCTCCGCCTTCCGGTTTCAAG A G RNF138 Ensembl:ENSG00000134758 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1432199183 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_31166,RMVar_hsa_circ_189493,RMVar_hsa_circ_298070,RMVar_hsa_circ_369840,RMVar_hsa_circ_303186,RMVar_hsa_circ_189495,RMVar_hsa_circ_189494,RMVar_hsa_circ_310815,RMVar_hsa_circ_324500,RMVar_hsa_circ_189496 10201 RMVar_ID_10201 Human_SNP_ID_642754823 A-to-I Human chr18 + 32121979 32121974 32121979 CAACCTCCGCCTTCCGGTTTCAAGCGATTCTCATGCCTCAGCCTCCCGAGTAGTTGGGATTACAG CAACCTCCGCCTTCCGGTTTCAAGCGAT_____TGCCTCAGCCTCCCGAGTAGTTGGGATTACAG TTCTCA T RNF138 Ensembl:ENSG00000134758 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1203925433 Functional Loss DEL dbSNP153 29..33 33 - - - RMVar_hsa_circ_31166,RMVar_hsa_circ_189493,RMVar_hsa_circ_298070,RMVar_hsa_circ_369840,RMVar_hsa_circ_303186,RMVar_hsa_circ_189495,RMVar_hsa_circ_189494,RMVar_hsa_circ_310815,RMVar_hsa_circ_324500,RMVar_hsa_circ_189496 10202 RMVar_ID_10202 Human_SNP_ID_642886963 A-to-I Human chr18 - 32684508 32684508 32684508 GGTAATGACAGAAAAATTTCATTTTAAGTTATAGACTGTTGCCTGGGTCAACCAGCCCATAGGAG GGTAATGACAGAAAAATTTCATTTTAAGTTATGGACTGTTGCCTGGGTCAACCAGCCCATAGGAG T C KLHL14 Ensembl:ENSG00000197705 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1019498474 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58236,RMVar_hsa_circ_367612 10203 RMVar_ID_10203 Human_SNP_ID_642886966 A-to-I Human chr18 - 32684515 32684515 32684515 GAAGCTTGGTAATGACAGAAAAATTTCATTTTAAGTTATAGACTGTTGCCTGGGTCAACCAGCCC GAAGCTTGGTAATGACAGAAAAATTTCATTTTGAGTTATAGACTGTTGCCTGGGTCAACCAGCCC T C KLHL14 Ensembl:ENSG00000197705 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs963865395 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58236,RMVar_hsa_circ_367612 10204 RMVar_ID_10204 Human_SNP_ID_643027088 A-to-I Human chr18 - 33287587 33287587 33287587 TTTGGTAGAGATGGGGTTTCGCCCTGTTGGCCAGACTGGTCTTGAACTCCTGACCTCAGGTGATC TTTGGTAGAGATGGGGTTTCGCCCTGTTGGCCGGACTGGTCTTGAACTCCTGACCTCAGGTGATC T C CCDC178 Ensembl:ENSG00000166960 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1363218535 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18401,RMVar_hsa_circ_349139 10205 RMVar_ID_10205 Human_SNP_ID_643456140 A-to-I Human chr18 + 35068876 35068876 35068876 GTGAAATAGTCTGTTTGATGCAATTGTCATATACTGGCATAACCTTTGGCAGCTGATGGGCTGTT GTGAAATAGTCTGTTTGATGCAATTGTCATATGCTGGCATAACCTTTGGCAGCTGATGGGCTGTT A G MAPRE2 Ensembl:ENSG00000166974 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1299701011 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_62149,RMVar_hsa_circ_122723,RMVar_hsa_circ_117421,RMVar_hsa_circ_189585,RMVar_hsa_circ_90460,RMVar_hsa_circ_189586,RMVar_hsa_circ_189588 10206 RMVar_ID_10206 Human_SNP_ID_643496904 A-to-I Human chr18 + 35245690 35245690 35245690 GTGGGAAGGCCTTTAGTTTGAGGTCCTATCTTATTATTCATCAGAGAATTCATAGTGGTGAGAAA GTGGGAAGGCCTTTAGTTTGAGGTCCTATCTTCTTATTCATCAGAGAATTCATAGTGGTGAGAAA A C ZNF397 Ensembl:ENSG00000186812 Protein coding CDS GSE56152 embryonic stem cells,wild type - 25708366 RNA-Seq:(High) rs755448255 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17908895,Human_RBP_ID_27671875 RMVar_hsa_circ_114926,RMVar_hsa_circ_189595 10207 RMVar_ID_10207 Human_SNP_ID_643497582 A-to-I Human chr18 + 35247810 35247810 35247810 CTCCTGCCTCAGCCTTCTGAGTAGCTGGGATTACAGGCATGCACCACCACAGCTGGCTAATTTTG CTCCTGCCTCAGCCTTCTGAGTAGCTGGGATTGCAGGCATGCACCACCACAGCTGGCTAATTTTG A G ZNF397 Ensembl:ENSG00000186812 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs561602353 Functional Loss SNV dbSNP153 33..33 33 - - - 10208 RMVar_ID_10208 Human_SNP_ID_643497597 A-to-I Human chr18 + 35247859 35247858 35247860 CAGCTGGCTAATTTTGTATTTTTAGGAAAGACAGGGTTTCTCCATGTTGGTCAGGCTGGTCTCGA CAGCTGGCTAATTTTGTATTTTTAGGAAAGAC__GGTTTCTCCATGTTGGTCAGGCTGGTCTCGA CAG C ZNF397 Ensembl:ENSG00000186812 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1406796879 Functional Loss DEL dbSNP153 33..34 33 - - - Human_miRNA_ID_976150 10209 RMVar_ID_10209 Human_SNP_ID_643497797 A-to-I Human chr18 + 35248583 35248583 35248583 AATAGATAGACCAAGCACAGTGGCTCACACCTATAATGCCAGCACTTTGGGAGGCCAAGGCTGGA AATAGATAGACCAAGCACAGTGGCTCACACCTGTAATGCCAGCACTTTGGGAGGCCAAGGCTGGA A G ZNF397 Ensembl:ENSG00000186812 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1060178 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25360765 10210 RMVar_ID_10210 Human_SNP_ID_643497806 A-to-I Human chr18 + 35248639 35248639 35248639 AAGGCTGGAGGATTGCTTGAGTCTAGGAGTTCAAGCCGAGCCTGGGCAGCATAGTGAGACCCCAT AAGGCTGGAGGATTGCTTGAGTCTAGGAGTTCGAGCCGAGCCTGGGCAGCATAGTGAGACCCCAT A G ZNF397 Ensembl:ENSG00000186812 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1137280 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6682051 10211 RMVar_ID_10211 Human_SNP_ID_643497813 A-to-I Human chr18 + 35248659 35248659 35248659 GTCTAGGAGTTCAAGCCGAGCCTGGGCAGCATAGTGAGACCCCATCTCTACAAAAAATAAACAGA GTCTAGGAGTTCAAGCCGAGCCTGGGCAGCATGGTGAGACCCCATCTCTACAAAAAATAAACAGA A G ZNF397 Ensembl:ENSG00000186812 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1137281 Functional Loss SNV dbSNP153 33..33 33 - - - 10212 RMVar_ID_10212 Human_SNP_ID_643497832 A-to-I Human chr18 + 35248708 35248708 35248708 ACAAAAAATAAACAGAATTTGCCAGACGTGGTAGTGCATGCCTGTAGACCCAAGTATTTGGGAGG ACAAAAAATAAACAGAATTTGCCAGACGTGGTGGTGCATGCCTGTAGACCCAAGTATTTGGGAGG A G ZNF397 Ensembl:ENSG00000186812 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,31158229,32596459 RNA-Seq:(High) rs1310121558 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6682052,Human_RBP_ID_13291038 10213 RMVar_ID_10213 Human_SNP_ID_643498052 A-to-I Human chr18 + 35249538 35249538 35249538 TAGCTGGTGTGGTGGCATGTGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGACAGGAGAATTGCA TAGCTGGTGTGGTGGCATGTGCCTGTAGTCCCCGCTACTTGGGAGGCTGAGACAGGAGAATTGCA A C ZNF397 Ensembl:ENSG00000186812 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1025635910 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1693952 10214 RMVar_ID_10214 Human_SNP_ID_643498923 A-to-I Human chr18 - 35252525 35252525 35252525 TGAAGACTCTTCTCTACTGCAGAAATTGTCATAGACCTAATTTTTAAAAAAATGAATCTGAAGGA TGAAGACTCTTCTCTACTGCAGAAATTGTCATTGACCTAATTTTTAAAAAAATGAATCTGAAGGA T A ZSCAN30 Ensembl:ENSG00000186814 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs988081405 Functional Loss SNV dbSNP153 33..33 33 - - - 10215 RMVar_ID_10215 Human_SNP_ID_643499140 A-to-I Human chr18 + 35253501 35253501 35253501 CTCTGATGCTGCATAAGGCCTGACCTATGCCTAAATGTTTTTCTACATTCACTACATTCATAAGG CTCTGATGCTGCATAAGGCCTGACCTATGCCTGAATGTTTTTCTACATTCACTACATTCATAAGG A G ZNF397 Ensembl:ENSG00000186812 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1261086458 Functional Loss SNV dbSNP153 33..33 33 - - - 10216 RMVar_ID_10216 Human_SNP_ID_643499910 A-to-I Human chr18 - 35256367 35256367 35256367 TTAGTAGAGATGGGGTTTTGCCATGTTGGCCAAGTTGGTTTTGAACTCCCCTGGCCTCAAGCGAT TTAGTAGAGATGGGGTTTTGCCATGTTGGCCAGGTTGGTTTTGAACTCCCCTGGCCTCAAGCGAT T C ZSCAN30 Ensembl:ENSG00000186814 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs981990348 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13291135 Human_Splice_Rec_1905255 10217 RMVar_ID_10217 Human_SNP_ID_643500426 A-to-I Human chr18 - 35258685 35258684 35258685 TTGTATTTTTAGTAGAGATGGGGTTTCACCATATTGGCCAGGCTGTTCTCAAACTCCTGACCTTG TTGTATTTTTAGTAGAGATGGGGTTTCACCAT_TTGGCCAGGCTGTTCTCAAACTCCTGACCTTG AT A ZSCAN30 Ensembl:ENSG00000186814 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1435504646 Functional Loss DEL dbSNP153 33..33 33 - - - 10218 RMVar_ID_10218 Human_SNP_ID_643500584 A-to-I Human chr18 - 35259259 35259259 35259259 TGAGCCCAGAAGGTGGAGGTTGCAGTGAGCTAAGATTGCGCCACTGCACTCCAGCCTGGATGACA TGAGCCCAGAAGGTGGAGGTTGCAGTGAGCTAGGATTGCGCCACTGCACTCCAGCCTGGATGACA T C ZSCAN30 Ensembl:ENSG00000186814 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1418706131 Functional Loss SNV dbSNP153 33..33 33 - - - 10219 RMVar_ID_10219 Human_SNP_ID_643500595 A-to-I Human chr18 - 35259320 35259320 35259320 AGGGATGGTGGTGCATGCCTATAGCCCCAGCTACTTGGGAGGCTGAGACAGGAGGGTCACCTGAG AGGGATGGTGGTGCATGCCTATAGCCCCAGCTGCTTGGGAGGCTGAGACAGGAGGGTCACCTGAG T C ZSCAN30 Ensembl:ENSG00000186814 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,cerebellum - 29129909,30559470 RNA-Seq:(High) rs1334865039 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25360790 10220 RMVar_ID_10220 Human_SNP_ID_643500598 A-to-I Human chr18 - 35259332 35259332 35259332 CAAAAATTAGCCAGGGATGGTGGTGCATGCCTATAGCCCCAGCTACTTGGGAGGCTGAGACAGGA CAAAAATTAGCCAGGGATGGTGGTGCATGCCTGTAGCCCCAGCTACTTGGGAGGCTGAGACAGGA T C ZSCAN30 Ensembl:ENSG00000186814 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1231037910 Functional Loss SNV dbSNP153 33..33 33 - - - 10221 RMVar_ID_10221 Human_SNP_ID_643500614 A-to-I Human chr18 - 35259385 35259385 35259385 ACTTGAGGTCAGGAGTTCAAGACCACTGTGAAACCCTGTCTTTACTAAAAATACAAAAATTAGCC ACTTGAGGTCAGGAGTTCAAGACCACTGTGAAGCCCTGTCTTTACTAAAAATACAAAAATTAGCC T C ZSCAN30 Ensembl:ENSG00000186814 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs552367858 Functional Loss SNV dbSNP153 33..33 33 - - - 10222 RMVar_ID_10222 Human_SNP_ID_643500624 A-to-I Human chr18 - 35259426 35259426 35259426 CCTGTAATGCCAGCGCTTTAAGAGGTTGAGGCAGGCAGATTACTTGAGGTCAGGAGTTCAAGACC CCTGTAATGCCAGCGCTTTAAGAGGTTGAGGCGGGCAGATTACTTGAGGTCAGGAGTTCAAGACC T C ZSCAN30 Ensembl:ENSG00000186814 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs776571999 Functional Loss SNV dbSNP153 33..33 33 - - - 10223 RMVar_ID_10223 Human_SNP_ID_643501401 A-to-I Human chr18 - 35263125 35263125 35263125 GTGATCCTCCTGCCTCAGCCTCCAGAGTAGCTAGGACTACAGTTGTACACCACCATGCCTGGCTA GTGATCCTCCTGCCTCAGCCTCCAGAGTAGCTGGGACTACAGTTGTACACCACCATGCCTGGCTA T C ZSCAN30 Ensembl:ENSG00000186814 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1160981809 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13291272 10224 RMVar_ID_10224 Human_SNP_ID_643501415 A-to-I Human chr18 - 35263225 35263225 35263225 CTTTTTTTTTTTTTTAGATGGGGTCTCACTCTATCACCCAGGTTGGAGTGCAGTGGTGCAACCAC CTTTTTTTTTTTTTTAGATGGGGTCTCACTCTGTCACCCAGGTTGGAGTGCAGTGGTGCAACCAC T C ZSCAN30 Ensembl:ENSG00000186814 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs772714434 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1905266 10225 RMVar_ID_10225 Human_SNP_ID_643513821 A-to-I Human chr18 + 35315951 35315951 35315951 AAAATATTAGTCGGGCATGGTGGCACGTGCCTATAGACCCAGCTACTCGGGAGGCTGAGACAGGA AAAATATTAGTCGGGCATGGTGGCACGTGCCTGTAGACCCAGCTACTCGGGAGGCTGAGACAGGA A G ZNF271P Ensembl:ENSG00000257267 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs951742109 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17381891 10226 RMVar_ID_10226 Human_SNP_ID_643672966 A-to-I Human chr18 + 35977125 35977115 35977125 AAGGCGCCTGGTCTCAGCTACATGGGAGGCTGAGGCAGGAGGATCACTTGAACCCAGGAGGCAGA AAGGCGCCTGGTCTCAGCTACAT__________GGCAGGAGGATCACTTGAACCCAGGAGGCAGA TGGGAGGCTGA T C18orf21 Ensembl:ENSG00000141428 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1011209526 Functional Loss DEL dbSNP153 24..33 33 - - - RMVar_hsa_circ_377887 10227 RMVar_ID_10227 Human_SNP_ID_643676022 A-to-I Human chr18 - 35990665 35990664 35990666 CATCTTTGAGTGCAGTTTGGTCTGACCCCTCAAGAGAAAAGCATGGTGCCGTAGGGCTGCTATGG CATCTTTGAGTGCAGTTTGGTCTGACCCCTC__GAGAAAAGCATGGTGCCGTAGGGCTGCTATGG CTT C RPRD1A Ensembl:ENSG00000141425 Protein coding intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs761125782 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_507918,Human_RBP_ID_6682960,Human_RBP_ID_13294368,Human_RBP_ID_17265135,Human_RBP_ID_17909138,Human_RBP_ID_18299122,Human_RBP_ID_23768004 Human_miRNA_ID_1689677,Human_miRNA_ID_2866511 RMVar_hsa_circ_84393,RMVar_hsa_circ_91796,RMVar_hsa_circ_92025,RMVar_hsa_circ_107226,RMVar_hsa_circ_189616,RMVar_hsa_circ_88193,RMVar_hsa_circ_189618,RMVar_hsa_circ_189620,RMVar_hsa_circ_80659,RMVar_hsa_circ_189621,RMVar_hsa_circ_189619,RMVar_hsa_circ_189617,RMVar_hsa_circ_351805 10228 RMVar_ID_10228 Human_SNP_ID_643679195 A-to-I Human chr18 - 36004383 36004383 36004383 GGGTGTGGTGGTGTGCGCCTGTAGTCCTAGCTACTCGGGAGGCAGAGGTGGGAGGATCATTTGAG GGGTGTGGTGGTGTGCGCCTGTAGTCCTAGCTGCTCGGGAGGCAGAGGTGGGAGGATCATTTGAG T C RPRD1A Ensembl:ENSG00000141425 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1380814792 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84393,RMVar_hsa_circ_91796,RMVar_hsa_circ_92025,RMVar_hsa_circ_107226,RMVar_hsa_circ_189616,RMVar_hsa_circ_88193,RMVar_hsa_circ_189618,RMVar_hsa_circ_189620,RMVar_hsa_circ_189621,RMVar_hsa_circ_189619 10229 RMVar_ID_10229 Human_SNP_ID_643682737 A-to-I Human chr18 - 36017251 36017251 36017251 TGTTACCCAGGTTGGAGCTCAGTGGCACAATCATGACTGACTGCACCCTCGACCTCCCAGGGCTC TGTTACCCAGGTTGGAGCTCAGTGGCACAATCGTGACTGACTGCACCCTCGACCTCCCAGGGCTC T C RPRD1A Ensembl:ENSG00000141425 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1455747225 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13295342,Human_RBP_ID_23768157 RMVar_hsa_circ_84393,RMVar_hsa_circ_91796,RMVar_hsa_circ_92025,RMVar_hsa_circ_107226,RMVar_hsa_circ_189616,RMVar_hsa_circ_88193,RMVar_hsa_circ_189618,RMVar_hsa_circ_189620,RMVar_hsa_circ_189621,RMVar_hsa_circ_189619 10230 RMVar_ID_10230 Human_SNP_ID_643683585 A-to-I Human chr18 - 36019988 36019988 36019988 TCACCCAGGCTGGACTGCAGTGGCGTGATCTCAGCTCGCTGCAACCTCTGCCTCCTGGGTTCAAG TCACCCAGGCTGGACTGCAGTGGCGTGATCTCCGCTCGCTGCAACCTCTGCCTCCTGGGTTCAAG T G RPRD1A Ensembl:ENSG00000141425 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs574852338 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84393,RMVar_hsa_circ_91796,RMVar_hsa_circ_92025,RMVar_hsa_circ_107226,RMVar_hsa_circ_189616,RMVar_hsa_circ_88193,RMVar_hsa_circ_189618,RMVar_hsa_circ_189620,RMVar_hsa_circ_189621,RMVar_hsa_circ_189619 10231 RMVar_ID_10231 Human_SNP_ID_643683598 A-to-I Human chr18 - 36020026 36020026 36020026 CCTTCCCCTTCCATTCTTTCAGATGGAGTCTCACTCTCTCACCCAGGCTGGACTGCAGTGGCGTG CCTTCCCCTTCCATTCTTTCAGATGGAGTCTCTCTCTCTCACCCAGGCTGGACTGCAGTGGCGTG T A RPRD1A Ensembl:ENSG00000141425 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs907673386 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20315960 RMVar_hsa_circ_84393,RMVar_hsa_circ_91796,RMVar_hsa_circ_92025,RMVar_hsa_circ_107226,RMVar_hsa_circ_189616,RMVar_hsa_circ_88193,RMVar_hsa_circ_189618,RMVar_hsa_circ_189620,RMVar_hsa_circ_189621,RMVar_hsa_circ_189619 10232 RMVar_ID_10232 Human_SNP_ID_643684069 A-to-I Human chr18 - 36021828 36021826 36021828 CCTGGCTAATTTTAAAATTTTTTTGTAGAGACAGGGTCTCACTATGTTGCCCAAGCTGGTCTTGA CCTGGCTAATTTTAAAATTTTTTTGTAGAGAC__GGTCTCACTATGTTGCCCAAGCTGGTCTTGA CCT C RPRD1A Ensembl:ENSG00000141425 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1218690868 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_84393,RMVar_hsa_circ_91796,RMVar_hsa_circ_92025,RMVar_hsa_circ_107226,RMVar_hsa_circ_189616,RMVar_hsa_circ_88193,RMVar_hsa_circ_189618,RMVar_hsa_circ_189620,RMVar_hsa_circ_189621,RMVar_hsa_circ_189619 10233 RMVar_ID_10233 Human_SNP_ID_643684370 A-to-I Human chr18 - 36022927 36022927 36022927 GAGACAGTCTCTTGTTCTGTCACCCAGGCTGGAGTAGTCATGCAATCACAGCTCACTGTAACCTC GAGACAGTCTCTTGTTCTGTCACCCAGGCTGGGGTAGTCATGCAATCACAGCTCACTGTAACCTC T C RPRD1A Ensembl:ENSG00000141425 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1292386900 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13295561,Human_RBP_ID_20316044,Human_RBP_ID_23768189 RMVar_hsa_circ_84393,RMVar_hsa_circ_91796,RMVar_hsa_circ_92025,RMVar_hsa_circ_107226,RMVar_hsa_circ_189616,RMVar_hsa_circ_88193,RMVar_hsa_circ_189618,RMVar_hsa_circ_189620,RMVar_hsa_circ_189621,RMVar_hsa_circ_189619 10234 RMVar_ID_10234 Human_SNP_ID_643684783 A-to-I Human chr18 - 36024428 36024428 36024428 TGTTGGGCCGGGTGTGGTGGTTCACGCCTGTAATCTCAGCACTTTGGGAAGCTGAGCTGGGTGAA TGTTGGGCCGGGTGTGGTGGTTCACGCCTGTAGTCTCAGCACTTTGGGAAGCTGAGCTGGGTGAA T C RPRD1A Ensembl:ENSG00000141425 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1349806292 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84393,RMVar_hsa_circ_91796,RMVar_hsa_circ_92025,RMVar_hsa_circ_107226,RMVar_hsa_circ_189616,RMVar_hsa_circ_88193,RMVar_hsa_circ_189618,RMVar_hsa_circ_189620,RMVar_hsa_circ_189621,RMVar_hsa_circ_189619 10235 RMVar_ID_10235 Human_SNP_ID_643686281 A-to-I Human chr18 - 36030078 36030078 36030078 AGAGTGGCCGGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGTCGGA AGAGTGGCCGGGCGCAGTGGCTCACGCCTGTACTCCCAGCACTTTGGGAGGCCAAGGTGGTCGGA T G RPRD1A Ensembl:ENSG00000141425 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1284738809 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91796,RMVar_hsa_circ_92025,RMVar_hsa_circ_107226,RMVar_hsa_circ_189616,RMVar_hsa_circ_189620,RMVar_hsa_circ_189621,RMVar_hsa_circ_274192,RMVar_hsa_circ_295175,RMVar_hsa_circ_314862,RMVar_hsa_circ_189625,RMVar_hsa_circ_189623,RMVar_hsa_circ_313358,RMVar_hsa_circ_189624 10236 RMVar_ID_10236 Human_SNP_ID_643686373 A-to-I Human chr18 - 36030396 36030396 36030396 TCACTGCAACCTCTGCCTCCTGGGTTCAAGCGATTCTCCTGCCTTAGCCTTCCAAATAGCTGAGA TCACTGCAACCTCTGCCTCCTGGGTTCAAGCGGTTCTCCTGCCTTAGCCTTCCAAATAGCTGAGA T C RPRD1A Ensembl:ENSG00000141425 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1255902004 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91796,RMVar_hsa_circ_92025,RMVar_hsa_circ_107226,RMVar_hsa_circ_189616,RMVar_hsa_circ_189620,RMVar_hsa_circ_189621,RMVar_hsa_circ_274192,RMVar_hsa_circ_295175,RMVar_hsa_circ_314862,RMVar_hsa_circ_189625,RMVar_hsa_circ_189623,RMVar_hsa_circ_313358,RMVar_hsa_circ_189624 10237 RMVar_ID_10237 Human_SNP_ID_643690334 A-to-I Human chr18 - 36046613 36046613 36046613 TGCCCCGGGCTGGCCTTGAACTCCTGACCTCAAGCAATCCACCCACCCCGGCCTCCGTATAGTGC TGCCCCGGGCTGGCCTTGAACTCCTGACCTCAGGCAATCCACCCACCCCGGCCTCCGTATAGTGC T C RPRD1A Ensembl:ENSG00000141425 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs566799410 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13296261 RMVar_hsa_circ_91796,RMVar_hsa_circ_189616,RMVar_hsa_circ_89204,RMVar_hsa_circ_189628 10238 RMVar_ID_10238 Human_SNP_ID_643718199 A-to-I Human chr18 + 36151138 36151138 36151138 ACAGTGTCTCACTCTGTTGCTCAGGCTGGGGTACAGTTGTGCAGTCATGGCTGACTGCAGTCTTG ACAGTGTCTCACTCTGTTGCTCAGGCTGGGGTGCAGTTGTGCAGTCATGGCTGACTGCAGTCTTG A G ELP2 Ensembl:ENSG00000134759 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1374417318 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238593 RMVar_hsa_circ_2640,RMVar_hsa_circ_340301,RMVar_hsa_circ_39164,RMVar_hsa_circ_12722,RMVar_hsa_circ_115881,RMVar_hsa_circ_189644,RMVar_hsa_circ_40813,RMVar_hsa_circ_21992,RMVar_hsa_circ_271669,RMVar_hsa_circ_189648,RMVar_hsa_circ_272323,RMVar_hsa_circ_60690,RMVar_hsa_circ_189652,RMVar_hsa_circ_189651,RMVar_hsa_circ_283550,RMVar_hsa_circ_366218,RMVar_hsa_circ_279740,RMVar_hsa_circ_189653,RMVar_hsa_circ_189654,RMVar_hsa_circ_332902,RMVar_hsa_circ_51443,RMVar_hsa_circ_348912,RMVar_hsa_circ_98969,RMVar_hsa_circ_189658 10239 RMVar_ID_10239 Human_SNP_ID_643718203 A-to-I Human chr18 + 36151148 36151148 36151148 ACTCTGTTGCTCAGGCTGGGGTACAGTTGTGCAGTCATGGCTGACTGCAGTCTTGACCTCCTGGG ACTCTGTTGCTCAGGCTGGGGTACAGTTGTGCCGTCATGGCTGACTGCAGTCTTGACCTCCTGGG A C ELP2 Ensembl:ENSG00000134759 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs966525144 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238593,Human_RBP_ID_13297864 RMVar_hsa_circ_2640,RMVar_hsa_circ_340301,RMVar_hsa_circ_39164,RMVar_hsa_circ_12722,RMVar_hsa_circ_115881,RMVar_hsa_circ_189644,RMVar_hsa_circ_40813,RMVar_hsa_circ_21992,RMVar_hsa_circ_271669,RMVar_hsa_circ_189648,RMVar_hsa_circ_272323,RMVar_hsa_circ_60690,RMVar_hsa_circ_189652,RMVar_hsa_circ_189651,RMVar_hsa_circ_283550,RMVar_hsa_circ_366218,RMVar_hsa_circ_279740,RMVar_hsa_circ_189653,RMVar_hsa_circ_189654,RMVar_hsa_circ_332902,RMVar_hsa_circ_51443,RMVar_hsa_circ_348912,RMVar_hsa_circ_98969,RMVar_hsa_circ_189658 10240 RMVar_ID_10240 Human_SNP_ID_643718262 A-to-I Human chr18 + 36151357 36151357 36151357 TACCCGCTTCTGCCTCCCAAAGTGCTGAGATTATAGGTGTGAGCCACCCTGACCTGCCCTGCCTT TACCCGCTTCTGCCTCCCAAAGTGCTGAGATTGTAGGTGTGAGCCACCCTGACCTGCCCTGCCTT A G ELP2 Ensembl:ENSG00000134759 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1168700687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13297867 RMVar_hsa_circ_2640,RMVar_hsa_circ_340301,RMVar_hsa_circ_39164,RMVar_hsa_circ_12722,RMVar_hsa_circ_115881,RMVar_hsa_circ_189644,RMVar_hsa_circ_40813,RMVar_hsa_circ_21992,RMVar_hsa_circ_271669,RMVar_hsa_circ_189648,RMVar_hsa_circ_272323,RMVar_hsa_circ_60690,RMVar_hsa_circ_189652,RMVar_hsa_circ_189651,RMVar_hsa_circ_283550,RMVar_hsa_circ_366218,RMVar_hsa_circ_279740,RMVar_hsa_circ_189653,RMVar_hsa_circ_189654,RMVar_hsa_circ_332902,RMVar_hsa_circ_51443,RMVar_hsa_circ_348912,RMVar_hsa_circ_98969,RMVar_hsa_circ_189658 10241 RMVar_ID_10241 Human_SNP_ID_643721906 A-to-I Human chr18 + 36165837 36165837 36165837 CTGGGAGGCAGAGGTTGCAGTGAGCCAAGATGATGCCATTGCACTCCAGCCTAGGCGACAGAGCA CTGGGAGGCAGAGGTTGCAGTGAGCCAAGATGTTGCCATTGCACTCCAGCCTAGGCGACAGAGCA A T ELP2 Ensembl:ENSG00000134759 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893164840 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13298518,Human_RBP_ID_25361542 RMVar_hsa_circ_115881,RMVar_hsa_circ_21992,RMVar_hsa_circ_189648,RMVar_hsa_circ_366218,RMVar_hsa_circ_28033,RMVar_hsa_circ_5121,RMVar_hsa_circ_189665,RMVar_hsa_circ_305463,RMVar_hsa_circ_326737,RMVar_hsa_circ_284437,RMVar_hsa_circ_189664,RMVar_hsa_circ_82774,RMVar_hsa_circ_189666,RMVar_hsa_circ_72782 10242 RMVar_ID_10242 Human_SNP_ID_643721910 A-to-I Human chr18 + 36165857 36165857 36165857 TGAGCCAAGATGATGCCATTGCACTCCAGCCTAGGCGACAGAGCAAGACCCCATCTTAACAAAAT TGAGCCAAGATGATGCCATTGCACTCCAGCCTGGGCGACAGAGCAAGACCCCATCTTAACAAAAT A G ELP2 Ensembl:ENSG00000134759 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1012991278 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13298519 RMVar_hsa_circ_115881,RMVar_hsa_circ_21992,RMVar_hsa_circ_189648,RMVar_hsa_circ_366218,RMVar_hsa_circ_28033,RMVar_hsa_circ_5121,RMVar_hsa_circ_189665,RMVar_hsa_circ_305463,RMVar_hsa_circ_326737,RMVar_hsa_circ_284437,RMVar_hsa_circ_189664,RMVar_hsa_circ_82774,RMVar_hsa_circ_189666,RMVar_hsa_circ_72782 10243 RMVar_ID_10243 Human_SNP_ID_643721949 A-to-I Human chr18 + 36166102 36166102 36166102 GTAATCCCCGCTACTCAGGAGGCTGAGACAGGAGGATTGCATGAACCCAGGAGATAAAGGTTGCA GTAATCCCCGCTACTCAGGAGGCTGAGACAGGCGGATTGCATGAACCCAGGAGATAAAGGTTGCA A C ELP2 Ensembl:ENSG00000134759 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs530165167 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5498444,Human_RBP_ID_6683685,Human_RBP_ID_13298527 RMVar_hsa_circ_115881,RMVar_hsa_circ_21992,RMVar_hsa_circ_189648,RMVar_hsa_circ_366218,RMVar_hsa_circ_28033,RMVar_hsa_circ_5121,RMVar_hsa_circ_189665,RMVar_hsa_circ_305463,RMVar_hsa_circ_326737,RMVar_hsa_circ_284437,RMVar_hsa_circ_189664,RMVar_hsa_circ_82774,RMVar_hsa_circ_189666,RMVar_hsa_circ_72782 10244 RMVar_ID_10244 Human_SNP_ID_643721950 A-to-I Human chr18 + 36166102 36166102 36166102 GTAATCCCCGCTACTCAGGAGGCTGAGACAGGAGGATTGCATGAACCCAGGAGATAAAGGTTGCA GTAATCCCCGCTACTCAGGAGGCTGAGACAGGGGGATTGCATGAACCCAGGAGATAAAGGTTGCA A G ELP2 Ensembl:ENSG00000134759 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs530165167 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5498444,Human_RBP_ID_6683685,Human_RBP_ID_13298527 RMVar_hsa_circ_115881,RMVar_hsa_circ_21992,RMVar_hsa_circ_189648,RMVar_hsa_circ_366218,RMVar_hsa_circ_28033,RMVar_hsa_circ_5121,RMVar_hsa_circ_189665,RMVar_hsa_circ_305463,RMVar_hsa_circ_326737,RMVar_hsa_circ_284437,RMVar_hsa_circ_189664,RMVar_hsa_circ_82774,RMVar_hsa_circ_189666,RMVar_hsa_circ_72782 10245 RMVar_ID_10245 Human_SNP_ID_643721951 A-to-I Human chr18 + 36166102 36166102 36166102 GTAATCCCCGCTACTCAGGAGGCTGAGACAGGAGGATTGCATGAACCCAGGAGATAAAGGTTGCA GTAATCCCCGCTACTCAGGAGGCTGAGACAGGTGGATTGCATGAACCCAGGAGATAAAGGTTGCA A T ELP2 Ensembl:ENSG00000134759 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs530165167 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5498444,Human_RBP_ID_6683685,Human_RBP_ID_13298527 RMVar_hsa_circ_115881,RMVar_hsa_circ_21992,RMVar_hsa_circ_189648,RMVar_hsa_circ_366218,RMVar_hsa_circ_28033,RMVar_hsa_circ_5121,RMVar_hsa_circ_189665,RMVar_hsa_circ_305463,RMVar_hsa_circ_326737,RMVar_hsa_circ_284437,RMVar_hsa_circ_189664,RMVar_hsa_circ_82774,RMVar_hsa_circ_189666,RMVar_hsa_circ_72782 10246 RMVar_ID_10246 Human_SNP_ID_643721956 A-to-I Human chr18 + 36166125 36166125 36166125 TGAGACAGGAGGATTGCATGAACCCAGGAGATAAAGGTTGCAGTGAGTGGAGATCCCACCACGGC TGAGACAGGAGGATTGCATGAACCCAGGAGATGAAGGTTGCAGTGAGTGGAGATCCCACCACGGC A G ELP2 Ensembl:ENSG00000134759 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1002993437 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5498444,Human_RBP_ID_13298528 RMVar_hsa_circ_115881,RMVar_hsa_circ_21992,RMVar_hsa_circ_189648,RMVar_hsa_circ_366218,RMVar_hsa_circ_28033,RMVar_hsa_circ_5121,RMVar_hsa_circ_189665,RMVar_hsa_circ_305463,RMVar_hsa_circ_326737,RMVar_hsa_circ_284437,RMVar_hsa_circ_189664,RMVar_hsa_circ_82774,RMVar_hsa_circ_189666,RMVar_hsa_circ_72782 10247 RMVar_ID_10247 Human_SNP_ID_643722139 A-to-I Human chr18 + 36166471 36166471 36166471 TCCTGCCTCAGCCTCCTGAGTAGCTGGGATTAAAGGCACCTGCTACCACACCTGGCTAATTTTTT TCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCACCTGCTACCACACCTGGCTAATTTTTT A C ELP2 Ensembl:ENSG00000134759 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1345409942 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115881,RMVar_hsa_circ_21992,RMVar_hsa_circ_189648,RMVar_hsa_circ_366218,RMVar_hsa_circ_28033,RMVar_hsa_circ_5121,RMVar_hsa_circ_189665,RMVar_hsa_circ_305463,RMVar_hsa_circ_326737,RMVar_hsa_circ_284437,RMVar_hsa_circ_189664,RMVar_hsa_circ_82774,RMVar_hsa_circ_189666,RMVar_hsa_circ_72782 10248 RMVar_ID_10248 Human_SNP_ID_643724911 A-to-I Human chr18 + 36177582 36177577 36177582 GATAAAAAGTCCTGTGGATTGGTTGCACAGTTAAGTTATGTGAATGCTGTATGCCAACTCAACTG GATAAAAAGTCCTGTGGATTGGTTGCAC_____AGTTATGTGAATGCTGTATGCCAACTCAACTG CAGTTA C ELP2 Ensembl:ENSG00000134759 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs983408679 Functional Loss DEL dbSNP153 29..33 33 - - - Human_RBP_ID_508286,Human_RBP_ID_13298889,Human_RBP_ID_23768664 10249 RMVar_ID_10249 Human_SNP_ID_643724913 A-to-I Human chr18 + 36177582 36177582 36177582 GATAAAAAGTCCTGTGGATTGGTTGCACAGTTAAGTTATGTGAATGCTGTATGCCAACTCAACTG GATAAAAAGTCCTGTGGATTGGTTGCACAGTTCAGTTATGTGAATGCTGTATGCCAACTCAACTG A C ELP2 Ensembl:ENSG00000134759 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs987398087 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_508286,Human_RBP_ID_13298889,Human_RBP_ID_23768664 10250 RMVar_ID_10250 Human_SNP_ID_643728947 A-to-I Human chr18 + 36192654 36192649 36192654 AAGTGACTCAGAATAGCCAAAGCAATCGTTTTATTTTATTTTTTGAGTCAGAGTCTCACTCTGTC AAGTGACTCAGAATAGCCAAAGCAATCG_____TTTTATTTTTTGAGTCAGAGTCTCACTCTGTC GTTTTA G MOCOS Ensembl:ENSG00000075643 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1253288014 Functional Loss DEL dbSNP153 29..33 33 - - - Human_RBP_ID_2539201 10251 RMVar_ID_10251 Human_SNP_ID_643728949 A-to-I Human chr18 + 36192659 36192659 36192659 ACTCAGAATAGCCAAAGCAATCGTTTTATTTTATTTTTTGAGTCAGAGTCTCACTCTGTCACAAA ACTCAGAATAGCCAAAGCAATCGTTTTATTTTGTTTTTTGAGTCAGAGTCTCACTCTGTCACAAA A G MOCOS Ensembl:ENSG00000075643 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs538728883 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2539201 10252 RMVar_ID_10252 Human_SNP_ID_643749291 A-to-I Human chr18 + 36270453 36270453 36270453 ATTAGGTCACTTGCCCAGGTGCGGTGGCTCACACCTGTAATTCCAGCACTTTGGGAGGCTGACGT ATTAGGTCACTTGCCCAGGTGCGGTGGCTCACGCCTGTAATTCCAGCACTTTGGGAGGCTGACGT A G MOCOS Ensembl:ENSG00000075643 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1454407683 Functional Loss SNV dbSNP153 33..33 33 - - - 10253 RMVar_ID_10253 Human_SNP_ID_643749423 A-to-I Human chr18 + 36270846 36270831 36270846 TCAGGCTTTTTGTTTTTTTGAGACAGGGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGCATG TCAGGCTTTTTGTTTTTT_______________CTCTGTCACCCAGGCTGGAGTGCAGTGGCATG TTGAGACAGGGTCTCA T MOCOS Ensembl:ENSG00000075643 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1191003893 Functional Loss DEL dbSNP153 19..33 33 - - - 10254 RMVar_ID_10254 Human_SNP_ID_643749424 A-to-I Human chr18 + 36270846 36270833 36270847 TCAGGCTTTTTGTTTTTTTGAGACAGGGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGCATG TCAGGCTTTTTGTTTTTTTG______________TCTGTCACCCAGGCTGGAGTGCAGTGGCATG GAGACAGGGTCTCAC G MOCOS Ensembl:ENSG00000075643 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1278097978 Functional Loss DEL dbSNP153 21..34 33 - - - 10255 RMVar_ID_10255 Human_SNP_ID_643776517 A-to-I Human chr18 + 36385662 36385662 36385662 GGCCTCAGGTGATCCGCCTGCCTTGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGGGC GGCCTCAGGTGATCCGCCTGCCTTGCCTCCCAGAGTGCTGGGATTACAGGCGTGAGCCACTGGGC A G FHOD3 Ensembl:ENSG00000134775 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1330045988 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4862,RMVar_hsa_circ_50640,RMVar_hsa_circ_29986,RMVar_hsa_circ_24915,RMVar_hsa_circ_46964,RMVar_hsa_circ_338354 10256 RMVar_ID_10256 Human_SNP_ID_643872329 A-to-I Human chr18 - 36781480 36781480 36781480 ACCCAGCTAATATTTATATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGATGGTCTCGA ACCCAGCTAATATTTATATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGATGGTCTCGA T C TPGS2 Ensembl:ENSG00000134779 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs531292413 Functional Loss SNV dbSNP153 33..33 33 - - - 10257 RMVar_ID_10257 Human_SNP_ID_643872344 A-to-I Human chr18 - 36781528 36781528 36781528 CCTGCTTCAGCCTCCCGAGTGACTGGGATTACAGGGATGTGCCACCACACCCAGCTAATATTTAT CCTGCTTCAGCCTCCCGAGTGACTGGGATTACCGGGATGTGCCACCACACCCAGCTAATATTTAT T G TPGS2 Ensembl:ENSG00000134779 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1354053532 Functional Loss SNV dbSNP153 33..33 33 - - - 10258 RMVar_ID_10258 Human_SNP_ID_643928107 A-to-I Human chr18 + 37020323 37020323 37020323 TTTTGTATTTTTAGTAGAGACAGGGTTTCACTATGTTGGCCAGGCTGGTCTTGAACTCTTGACCT TTTTGTATTTTTAGTAGAGACAGGGTTTCACTGTGTTGGCCAGGCTGGTCTTGAACTCTTGACCT A G KIAA1328 Ensembl:ENSG00000150477 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs752702676 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_325485,RMVar_hsa_circ_10826,RMVar_hsa_circ_345037,RMVar_hsa_circ_316792,RMVar_hsa_circ_362733,RMVar_hsa_circ_367287,RMVar_hsa_circ_356147 10259 RMVar_ID_10259 Human_SNP_ID_643981318 A-to-I Human chr18 - 37244592 37244592 37244592 GCGATTCTATGAAAAAATGTAATAAAAAATTAAAAAAAAAACAAAAAACAAAAAAAACAACAAAA GCGATTCTATGAAAAAATGTAATAAAAAATTATAAAAAAAACAAAAAACAAAAAAAACAACAAAA T A CELF4 Ensembl:ENSG00000101489 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs904161576 Functional Loss SNV dbSNP153 33..33 33 - - - 10260 RMVar_ID_10260 Human_SNP_ID_643986501 A-to-I Human chr18 - 37265791 37265791 37265791 CCAGTGCTGTCTCCCATGAGTGCAGTGGGGCTACCTGGCAAGGGGTGAGGGGACTGAGGTGAAGC CCAGTGCTGTCTCCCATGAGTGCAGTGGGGCTGCCTGGCAAGGGGTGAGGGGACTGAGGTGAAGC T C CELF4 Ensembl:ENSG00000101489 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs970520453 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_662 10261 RMVar_ID_10261 Human_SNP_ID_644489821 A-to-I Human chr18 - 39335703 39335703 39335703 CAACACGGTGAAACCCCATCCCTAATAAAAATATAAAAATTAGCTCTCCTCCCGCCGCCCAAGAT CAACACGGTGAAACCCCATCCCTAATAAAAATGTAAAAATTAGCTCTCCTCCCGCCGCCCAAGAT T C MIR924HG Ensembl:ENSG00000267374 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs974804665 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80662,RMVar_hsa_circ_189740 10262 RMVar_ID_10262 Human_SNP_ID_644504571 A-to-I Human chr18 - 39398708 39398708 39398708 GAAATTAGCTGGGTTTGGTGGTGCACCCTGTAATCCTAGCTACTCGGGGGGCTGAGGCACAAGAA GAAATTAGCTGGGTTTGGTGGTGCACCCTGTAGTCCTAGCTACTCGGGGGGCTGAGGCACAAGAA T C MIR924HG Ensembl:ENSG00000267374 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs760208432 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80662,RMVar_hsa_circ_189740 10263 RMVar_ID_10263 Human_SNP_ID_644505615 A-to-I Human chr18 - 39402665 39402665 39402665 CTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCGCGTGCCACTGCACCCAGCTAATTTTT CTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTCCAGGCGCGTGCCACTGCACCCAGCTAATTTTT T G MIR924HG Ensembl:ENSG00000267374 lincRNA intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs955358879 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80662,RMVar_hsa_circ_189740 10264 RMVar_ID_10264 Human_SNP_ID_644537268 A-to-I Human chr18 - 39532060 39532060 39532060 AAGATAAGTACTTGGCTGACCCCAGAAGTGCAAAGCTGACTGTAAAGCTCACCTTCTTTCCATAT AAGATAAGTACTTGGCTGACCCCAGAAGTGCACAGCTGACTGTAAAGCTCACCTTCTTTCCATAT T G MIR924HG Ensembl:ENSG00000267374 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1373868162 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80662,RMVar_hsa_circ_189740 10265 RMVar_ID_10265 Human_SNP_ID_645160049 A-to-I Human chr18 + 41975907 41975907 41975907 TATTTTTAGTAGAAATGGGGCTTCATTGTGTTAGCCAGGCTGGTCTTGAACTCCTGACCTCGTGA TATTTTTAGTAGAAATGGGGCTTCATTGTGTTTGCCAGGCTGGTCTTGAACTCCTGACCTCGTGA A T PIK3C3 Ensembl:ENSG00000078142 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs976201346 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39594,RMVar_hsa_circ_30553,RMVar_hsa_circ_353193 10266 RMVar_ID_10266 Human_SNP_ID_645177491 A-to-I Human chr18 + 42047549 42047549 42047549 GCAGTGCTACTTAAAGTGTGATCTGTGGACCCACAGTATTGACTTTACCTGGGAGCTTGTTTGTA GCAGTGCTACTTAAAGTGTGATCTGTGGACCCGCAGTATTGACTTTACCTGGGAGCTTGTTTGTA A G PIK3C3 Ensembl:ENSG00000078142 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903910646 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_310982,RMVar_hsa_circ_19703,RMVar_hsa_circ_371909,RMVar_hsa_circ_32988,RMVar_hsa_circ_189755,RMVar_hsa_circ_189756,RMVar_hsa_circ_347952,RMVar_hsa_circ_370492,RMVar_hsa_circ_307209,RMVar_hsa_circ_189760,RMVar_hsa_circ_103757,RMVar_hsa_circ_189763,RMVar_hsa_circ_329480,RMVar_hsa_circ_274077,RMVar_hsa_circ_29040,RMVar_hsa_circ_281162,RMVar_hsa_circ_264845,RMVar_hsa_circ_38265,RMVar_hsa_circ_189776,RMVar_hsa_circ_189771,RMVar_hsa_circ_189772,RMVar_hsa_circ_189773,RMVar_hsa_circ_317204,RMVar_hsa_circ_281212,RMVar_hsa_circ_55328,RMVar_hsa_circ_274137,RMVar_hsa_circ_342618,RMVar_hsa_circ_189775,RMVar_hsa_circ_373495,RMVar_hsa_circ_311602,RMVar_hsa_circ_189778,RMVar_hsa_circ_189779,RMVar_hsa_circ_189777,RMVar_hsa_circ_189783,RMVar_hsa_circ_189782,RMVar_hsa_circ_189781,RMVar_hsa_circ_278725,RMVar_hsa_circ_308476,RMVar_hsa_circ_342471,RMVar_hsa_circ_285080,RMVar_hsa_circ_325861,RMVar_hsa_circ_328006,RMVar_hsa_circ_189784 10267 RMVar_ID_10267 Human_SNP_ID_645870268 A-to-I Human chr18 + 44771330 44771330 44771330 CAGAGGCTGGTGTGGTTTCGTCTACCTGGTCTAGATGGTGCATGGGTGCACAGGTGGTGTCAGGT CAGAGGCTGGTGTGGTTTCGTCTACCTGGTCTGGATGGTGCATGGGTGCACAGGTGGTGTCAGGT A G SETBP1 Ensembl:ENSG00000152217 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs929129047 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_281656,RMVar_hsa_circ_189809,RMVar_hsa_circ_189810,RMVar_hsa_circ_189808 10268 RMVar_ID_10268 Human_SNP_ID_384112461 A-to-I Human chr8 + 136635598 136635598 136635598 AATTTTTGTATTTTTTGTAGAGAAGGGATTTCACCACGTTGACTGGGCTGGTCTCTAACTTCTAG AATTTTTGTATTTTTTGTAGAGAAGGGATTTCGCCACGTTGACTGGGCTGGTCTCTAACTTCTAG A G LINC02055 Ensembl:ENSG00000254101 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1036501111 Functional Loss SNV dbSNP153 33..33 33 - - - 10269 RMVar_ID_10269 Human_SNP_ID_384112468 A-to-I Human chr8 + 136635622 136635622 136635622 GGGATTTCACCACGTTGACTGGGCTGGTCTCTAACTTCTAGATTCAAGCAATTCACCTGCCTCGG GGGATTTCACCACGTTGACTGGGCTGGTCTCTGACTTCTAGATTCAAGCAATTCACCTGCCTCGG A G LINC02055 Ensembl:ENSG00000254101 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1377254652 Functional Loss SNV dbSNP153 33..33 33 - - - 10270 RMVar_ID_10270 Human_SNP_ID_384134769 A-to-I Human chr8 + 136727731 136727731 136727731 GCTTCAGAGAGAATAAATTGTAAATGTTTCTTATCAGACTTAAGGTCCATGTTAATGTTAAATGC GCTTCAGAGAGAATAAATTGTAAATGTTTCTTGTCAGACTTAAGGTCCATGTTAATGTTAAATGC A G LINC02055 Ensembl:ENSG00000254101 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs755586858 Functional Loss SNV dbSNP153 33..33 33 - - - 10271 RMVar_ID_10271 Human_SNP_ID_384135482 A-to-I Human chr8 + 136730875 136730875 136730875 ACACAGACTTTAAGTCTGATAAGACACATTTTACAACCTATTCTCTCTGAAGCCTGTGAGCTAAA ACACAGACTTTAAGTCTGATAAGACACATTTTGCAACCTATTCTCTCTGAAGCCTGTGAGCTAAA A G LINC02055 Ensembl:ENSG00000254101 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1194231834 Functional Loss SNV dbSNP153 33..33 33 - - - 10272 RMVar_ID_10272 Human_SNP_ID_384135493 A-to-I Human chr8 + 136730922 136730922 136730922 TGAAGCCTGTGAGCTAAAAGCTTCATCTGTATAGTAAAACTGTGGTCTCTGCAACCTGTTATCGC TGAAGCCTGTGAGCTAAAAGCTTCATCTGTATGGTAAAACTGTGGTCTCTGCAACCTGTTATCGC A G LINC02055 Ensembl:ENSG00000254101 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs763826480 Functional Loss SNV dbSNP153 33..33 33 - - - 10273 RMVar_ID_10273 Human_SNP_ID_384942778 A-to-I Human chr8 - 139819961 139819961 139819961 CTCTGTCGCCCAGGCTGGAGTGCAGTGGCACAATCTTGGCTCACTGCAACCTCTGCCTCCCGGGG CTCTGTCGCCCAGGCTGGAGTGCAGTGGCACAGTCTTGGCTCACTGCAACCTCTGCCTCCCGGGG T C TRAPPC9 Ensembl:ENSG00000167632 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1291970228 Functional Loss SNV dbSNP153 33..33 33 - - - 10274 RMVar_ID_10274 Human_SNP_ID_385010158 A-to-I Human chr8 - 140077083 140077083 140077083 AGGCTCACTGTATCCTTTACCTCCTGGGTTCAAGCGATCCTCCTGCCTCAGCCTCCCGAGTGGCT AGGCTCACTGTATCCTTTACCTCCTGGGTTCAGGCGATCCTCCTGCCTCAGCCTCCCGAGTGGCT T C TRAPPC9 Ensembl:ENSG00000167632 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1434776904 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71575 10275 RMVar_ID_10275 Human_SNP_ID_385037260 A-to-I Human chr8 - 140183629 140183629 140183629 GTCTCGAACCCCTGACCTCAGGTGATCTGCCCACCTTGGCCTCCCAAAGTGCTGGGATTATGGGA GTCTCGAACCCCTGACCTCAGGTGATCTGCCCGCCTTGGCCTCCCAAAGTGCTGGGATTATGGGA T C TRAPPC9 Ensembl:ENSG00000167632 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1378234536 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71575 10276 RMVar_ID_10276 Human_SNP_ID_385037277 A-to-I Human chr8 - 140183692 140183692 140183692 CACCACCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGACGTTTCACCATTTGGCCAGGCTGGT CACCACCATGCCCAGCTAATTTTTGTATTTTTGGTAGAGACGTTTCACCATTTGGCCAGGCTGGT T C TRAPPC9 Ensembl:ENSG00000167632 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1322505259 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71575 10277 RMVar_ID_10277 Human_SNP_ID_385037687 A-to-I Human chr8 - 140184600 140184600 140184600 TACTAAAAATAAAACAAAACAAAACAAAAATTAGTCAGGCATGGTGGCTTACTCCTGTAATCCCA TACTAAAAATAAAACAAAACAAAACAAAAATTTGTCAGGCATGGTGGCTTACTCCTGTAATCCCA T A TRAPPC9 Ensembl:ENSG00000167632 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1380379964 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71575 10278 RMVar_ID_10278 Human_SNP_ID_385075305 A-to-I Human chr8 - 140333453 140333453 140333453 GGGAGGCGGAGGTTGCAACGAGCTGAGATCGCACCATTGCACTCCAGCCTGGGCGACAAGAGTGA GGGAGGCGGAGGTTGCAACGAGCTGAGATCGCGCCATTGCACTCCAGCCTGGGCGACAAGAGTGA T C TRAPPC9 Ensembl:ENSG00000167632 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1379567955 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122308,RMVar_hsa_circ_79986,RMVar_hsa_circ_254638,RMVar_hsa_circ_254636,RMVar_hsa_circ_254637,RMVar_hsa_circ_11706,RMVar_hsa_circ_323729,RMVar_hsa_circ_8773,RMVar_hsa_circ_345554,RMVar_hsa_circ_254648,RMVar_hsa_circ_97711,RMVar_hsa_circ_254650,RMVar_hsa_circ_18594,RMVar_hsa_circ_368201,RMVar_hsa_circ_60324,RMVar_hsa_circ_327434,RMVar_hsa_circ_254653,RMVar_hsa_circ_254655,RMVar_hsa_circ_345561,RMVar_hsa_circ_370921,RMVar_hsa_circ_340247,RMVar_hsa_circ_254654 10279 RMVar_ID_10279 Human_SNP_ID_385094489 A-to-I Human chr8 - 140410055 140410055 140410055 CTCACTGCAGCCTTGGCCTTCTGGGCTCAAGCAGTCCTCCTGCCTCAGCCTCCCAAGTAGCTGGG CTCACTGCAGCCTTGGCCTTCTGGGCTCAAGCGGTCCTCCTGCCTCAGCCTCCCAAGTAGCTGGG T C TRAPPC9 Ensembl:ENSG00000167632 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs972904265 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79986,RMVar_hsa_circ_254637,RMVar_hsa_circ_17276,RMVar_hsa_circ_60324,RMVar_hsa_circ_254655,RMVar_hsa_circ_370921,RMVar_hsa_circ_45325,RMVar_hsa_circ_254664,RMVar_hsa_circ_280909,RMVar_hsa_circ_339914,RMVar_hsa_circ_254665,RMVar_hsa_circ_76202,RMVar_hsa_circ_254666 10280 RMVar_ID_10280 Human_SNP_ID_385119554 A-to-I Human chr8 - 140502175 140502175 140502175 TTTAAAGACATTTCAATTTCACCATGCTGGCCAGGCTGGTCTTCAACTCCTGACCTTAGGTGATC TTTAAAGACATTTCAATTTCACCATGCTGGCCTGGCTGGTCTTCAACTCCTGACCTTAGGTGATC T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs896383777 Functional Loss SNV dbSNP153 33..33 33 - - - 10281 RMVar_ID_10281 Human_SNP_ID_385119555 A-to-I Human chr8 - 140502175 140502175 140502175 TTTAAAGACATTTCAATTTCACCATGCTGGCCAGGCTGGTCTTCAACTCCTGACCTTAGGTGATC TTTAAAGACATTTCAATTTCACCATGCTGGCCGGGCTGGTCTTCAACTCCTGACCTTAGGTGATC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs896383777 Functional Loss SNV dbSNP153 33..33 33 - - - 10282 RMVar_ID_10282 Human_SNP_ID_385120910 A-to-I Human chr8 - 140506868 140506868 140506868 AGATCATGAGAGCAGGAATTTGAGATCGGCCTAGCCAATATGGTGAAACCCCGTCTCTACTAAAA AGATCATGAGAGCAGGAATTTGAGATCGGCCTGGCCAATATGGTGAAACCCCGTCTCTACTAAAA T C AC107375.1 Ensembl:ENSG00000259891 lincRNA exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs544515027 Functional Loss SNV dbSNP153 33..33 33 - - - 10283 RMVar_ID_10283 Human_SNP_ID_385121750 A-to-I Human chr8 - 140509645 140509645 140509645 CAGCCCAACCAATATAGTCAAACCCCATCTCTACTGAAATTATTAAAATTAGCTGGGCGTGGTGG CAGCCCAACCAATATAGTCAAACCCCATCTCTGCTGAAATTATTAAAATTAGCTGGGCGTGGTGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1219746360 Functional Loss SNV dbSNP153 33..33 33 - - - 10284 RMVar_ID_10284 Human_SNP_ID_385121752 A-to-I Human chr8 - 140509651 140509651 140509651 CGAGACCAGCCCAACCAATATAGTCAAACCCCATCTCTACTGAAATTATTAAAATTAGCTGGGCG CGAGACCAGCCCAACCAATATAGTCAAACCCCTTCTCTACTGAAATTATTAAAATTAGCTGGGCG T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1311007732 Functional Loss SNV dbSNP153 33..33 33 - - - 10285 RMVar_ID_10285 Human_SNP_ID_385121753 A-to-I Human chr8 - 140509651 140509651 140509651 CGAGACCAGCCCAACCAATATAGTCAAACCCCATCTCTACTGAAATTATTAAAATTAGCTGGGCG CGAGACCAGCCCAACCAATATAGTCAAACCCCGTCTCTACTGAAATTATTAAAATTAGCTGGGCG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1311007732 Functional Loss SNV dbSNP153 33..33 33 - - - 10286 RMVar_ID_10286 Human_SNP_ID_385121942 A-to-I Human chr8 - 140510312 140510312 140510312 CTCACTGCAACCTCCAACACCCCGATTCAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGG CTCACTGCAACCTCCAACACCCCGATTCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs931208989 Functional Loss SNV dbSNP153 33..33 33 - - - 10287 RMVar_ID_10287 Human_SNP_ID_385124028 A-to-I Human chr8 + 140516329 140516329 140516329 GCCACCATGCCCAACCTATTTTTGTATTTTTTAGTAGAGACGGGGTTCACCATGTTGGCCAGGCT GCCACCATGCCCAACCTATTTTTGTATTTTTTGGTAGAGACGGGGTTCACCATGTTGGCCAGGCT A G CHRAC1 Ensembl:ENSG00000104472 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs997707933 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_795476,Human_RBP_ID_16370217 RMVar_hsa_circ_111855,RMVar_hsa_circ_254669 10288 RMVar_ID_10288 Human_SNP_ID_385124038 A-to-I Human chr8 + 140516368 140516367 140516368 ACGGGGTTCACCATGTTGGCCAGGCTTGTCTCAAACTCCTAACCTCAACTGATCCACCTGCCTCA ACGGGGTTCACCATGTTGGCCAGGCTTGTCTC_AACTCCTAACCTCAACTGATCCACCTGCCTCA CA C CHRAC1 Ensembl:ENSG00000104472 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1340473531 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_24441589,Human_RBP_ID_26553813 RMVar_hsa_circ_111855,RMVar_hsa_circ_254669 10289 RMVar_ID_10289 Human_SNP_ID_385131268 A-to-I Human chr8 - 140543584 140543584 140543584 GGGGGTGGTGGCGTGCGCCTGTAGTTCCTGCTACCTAGGAGGCTGAGGTGAGAGGATTGCCAGAG GGGGGTGGTGGCGTGCGCCTGTAGTTCCTGCTCCCTAGGAGGCTGAGGTGAGAGGATTGCCAGAG T G AGO2 Ensembl:ENSG00000123908 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917259763 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16371049 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_20987,RMVar_hsa_circ_16504,RMVar_hsa_circ_254675,RMVar_hsa_circ_4690 10290 RMVar_ID_10290 Human_SNP_ID_385150788 A-to-I Human chr8 - 140613078 140613078 140613078 CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACGGGCGTCTGCCACCACACCTGGCTAATTATT CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTGCGGGCGTCTGCCACCACACCTGGCTAATTATT T C AGO2 Ensembl:ENSG00000123908 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1168458068 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_180711 10291 RMVar_ID_10291 Human_SNP_ID_385152053 A-to-I Human chr8 - 140617994 140617994 140617994 TGGCCCAACTTTTTTTTTTTGTAGACGGTCTCACTCTGTTGCCCAGGCTGGAGTGCAGTGGTGCA TGGCCCAACTTTTTTTTTTTGTAGACGGTCTCGCTCTGTTGCCCAGGCTGGAGTGCAGTGGTGCA T C AGO2 Ensembl:ENSG00000123908 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335452654 Functional Loss SNV dbSNP153 33..33 33 - - - 10292 RMVar_ID_10292 Human_SNP_ID_385152822 A-to-I Human chr8 - 140620808 140620808 140620808 CTCTGACAACCAAGCTGGCTTGCAGTGGCACAATCTCAGCTCAGTGCAGCCTCTGCCTCCCTTGC CTCTGACAACCAAGCTGGCTTGCAGTGGCACAGTCTCAGCTCAGTGCAGCCTCTGCCTCCCTTGC T C AGO2 Ensembl:ENSG00000123908 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs111366603 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16371921 10293 RMVar_ID_10293 Human_SNP_ID_385163255 A-to-I Human chr8 - 140660650 140660650 140660650 ACGATCTTGGCTCACTACAACCTCTGTCTTCCAGGCTCAAGCCGTCCTCCCACGTCAGCCTCCTG ACGATCTTGGCTCACTACAACCTCTGTCTTCCGGGCTCAAGCCGTCCTCCCACGTCAGCCTCCTG T C PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs777820055 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1016603 RMVar_hsa_circ_84244,RMVar_hsa_circ_101087,RMVar_hsa_circ_254694,RMVar_hsa_circ_254695 10294 RMVar_ID_10294 Human_SNP_ID_385165840 A-to-I Human chr8 - 140670308 140670308 140670308 GGATTACAGGGATGCACTACCATTACCCTGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTGA GGATTACAGGGATGCACTACCATTACCCTGCTGATTTTTGTATTTTTAGTAGAGACAGGGTTTGA T C PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs919670400 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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,RMVar_hsa_circ_254703,RMVar_hsa_circ_120136 10295 RMVar_ID_10295 Human_SNP_ID_385166250 A-to-I Human chr8 - 140671373 140671373 140671373 TACTAAAAATACAAACATTAGCTGTGCATAGTAGTGTGACCCTATAATTCCAGCTGCTCAGGGGG TACTAAAAATACAAACATTAGCTGTGCATAGTCGTGTGACCCTATAATTCCAGCTGCTCAGGGGG T G PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1199234696 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16372428 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_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,RMVar_hsa_circ_254703,RMVar_hsa_circ_120136 10296 RMVar_ID_10296 Human_SNP_ID_385166439 A-to-I Human chr8 - 140671926 140671926 140671926 GTAAAGATTCCCGCCCCCCGCCCCCCTGAGACAGAGTCTCACTCTGTTGCCCAGGCTGGAGTGCA GTAAAGATTCCCGCCCCCCGCCCCCCTGAGACGGAGTCTCACTCTGTTGCCCAGGCTGGAGTGCA T C PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935170567 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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,RMVar_hsa_circ_254703,RMVar_hsa_circ_120136 10297 RMVar_ID_10297 Human_SNP_ID_385172035 A-to-I Human chr8 - 140692877 140692877 140692877 TGAATGAAAGATGAATGCCGAGACGGGGAACTAAAGAGCAGTGGCAAGAGGCTGTCTGTCTGAAG TGAATGAAAGATGAATGCCGAGACGGGGAACTGAAGAGCAGTGGCAAGAGGCTGTCTGTCTGAAG T C PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1304824540 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 10298 RMVar_ID_10298 Human_SNP_ID_385172049 A-to-I Human chr8 - 140692917 140692917 140692917 ATGTGAGCATTTTTCCCTCACATAGCAGATCCAGTCAGTCTGAATGAAAGATGAATGCCGAGACG ATGTGAGCATTTTTCCCTCACATAGCAGATCCGGTCAGTCTGAATGAAAGATGAATGCCGAGACG T C PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs748520660 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16372636,Human_RBP_ID_17578760 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 10299 RMVar_ID_10299 Human_SNP_ID_385172058 A-to-I Human chr8 - 140692972 140692972 140692972 TTAAATGAGAAAGCCCTATCTATATAAAGCCTACTTTGTGTTTTGAGAAAGAAATATGTGAGCAT TTAAATGAGAAAGCCCTATCTATATAAAGCCTGCTTTGTGTTTTGAGAAAGAAATATGTGAGCAT T C PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs770207562 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17578760 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 10300 RMVar_ID_10300 Human_SNP_ID_385172059 A-to-I Human chr8 - 140692981 140692981 140692981 ATTTTAATTTTAAATGAGAAAGCCCTATCTATATAAAGCCTACTTTGTGTTTTGAGAAAGAAATA ATTTTAATTTTAAATGAGAAAGCCCTATCTATTTAAAGCCTACTTTGTGTTTTGAGAAAGAAATA T A PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs989478553 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17578760 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 10301 RMVar_ID_10301 Human_SNP_ID_385185676 A-to-I Human chr8 - 140746993 140746993 140746993 CCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCCAGGAGGTGGAGGTTGCAATGAGT CCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCAGGAGGTGGAGGTTGCAATGAGT T C PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs768901755 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_99024,RMVar_hsa_circ_119341,RMVar_hsa_circ_89446,RMVar_hsa_circ_9428,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_254703,RMVar_hsa_circ_120136,RMVar_hsa_circ_10045,RMVar_hsa_circ_108356,RMVar_hsa_circ_24582,RMVar_hsa_circ_85561,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_43746,RMVar_hsa_circ_254708,RMVar_hsa_circ_254709,RMVar_hsa_circ_331571,RMVar_hsa_circ_355189,RMVar_hsa_circ_372200,RMVar_hsa_circ_324678,RMVar_hsa_circ_322054,RMVar_hsa_circ_289176,RMVar_hsa_circ_100311,RMVar_hsa_circ_55128,RMVar_hsa_circ_62919,RMVar_hsa_circ_18874,RMVar_hsa_circ_254710,RMVar_hsa_circ_254712,RMVar_hsa_circ_254713,RMVar_hsa_circ_254711,RMVar_hsa_circ_102318,RMVar_hsa_circ_118455,RMVar_hsa_circ_116780,RMVar_hsa_circ_254720,RMVar_hsa_circ_254718,RMVar_hsa_circ_254719,RMVar_hsa_circ_79843,RMVar_hsa_circ_301995,RMVar_hsa_circ_345993,RMVar_hsa_circ_293517,RMVar_hsa_circ_50439,RMVar_hsa_circ_68510,RMVar_hsa_circ_34510,RMVar_hsa_circ_19337,RMVar_hsa_circ_36824,RMVar_hsa_circ_46062,RMVar_hsa_circ_254724,RMVar_hsa_circ_14253,RMVar_hsa_circ_254723,RMVar_hsa_circ_364371,RMVar_hsa_circ_342408,RMVar_hsa_circ_329586,RMVar_hsa_circ_312100,RMVar_hsa_circ_271231,RMVar_hsa_circ_270866,RMVar_hsa_circ_291797,RMVar_hsa_circ_335902,RMVar_hsa_circ_254726,RMVar_hsa_circ_376365,RMVar_hsa_circ_254725,RMVar_hsa_circ_378315,RMVar_hsa_circ_339697,RMVar_hsa_circ_298567,RMVar_hsa_circ_52177,RMVar_hsa_circ_270177,RMVar_hsa_circ_42162,RMVar_hsa_circ_254730,RMVar_hsa_circ_254732,RMVar_hsa_circ_254733,RMVar_hsa_circ_254734,RMVar_hsa_circ_254731,RMVar_hsa_circ_293992,RMVar_hsa_circ_311115,RMVar_hsa_circ_363588,RMVar_hsa_circ_298473,RMVar_hsa_circ_40870,RMVar_hsa_circ_54342,RMVar_hsa_circ_63759,RMVar_hsa_circ_254735,RMVar_hsa_circ_254737,RMVar_hsa_circ_254738,RMVar_hsa_circ_254736,RMVar_hsa_circ_254741,RMVar_hsa_circ_75783,RMVar_hsa_circ_77007,RMVar_hsa_circ_26426,RMVar_hsa_circ_332185,RMVar_hsa_circ_254740,RMVar_hsa_circ_340154,RMVar_hsa_circ_284585,RMVar_hsa_circ_48382,RMVar_hsa_circ_254742 10302 RMVar_ID_10302 Human_SNP_ID_385186800 A-to-I Human chr8 - 140750993 140750993 140750993 CTCCCATCTCGGGGCTGCAAATACCTGGTACTACAGATGGGCGCCACCACATCCAGCTAATTTTT CTCCCATCTCGGGGCTGCAAATACCTGGTACTGCAGATGGGCGCCACCACATCCAGCTAATTTTT T C PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs943757665 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_99024,RMVar_hsa_circ_119341,RMVar_hsa_circ_89446,RMVar_hsa_circ_9428,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_254703,RMVar_hsa_circ_120136,RMVar_hsa_circ_10045,RMVar_hsa_circ_108356,RMVar_hsa_circ_24582,RMVar_hsa_circ_85561,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_43746,RMVar_hsa_circ_254708,RMVar_hsa_circ_254709,RMVar_hsa_circ_331571,RMVar_hsa_circ_355189,RMVar_hsa_circ_372200,RMVar_hsa_circ_324678,RMVar_hsa_circ_322054,RMVar_hsa_circ_289176,RMVar_hsa_circ_100311,RMVar_hsa_circ_55128,RMVar_hsa_circ_62919,RMVar_hsa_circ_18874,RMVar_hsa_circ_254710,RMVar_hsa_circ_254712,RMVar_hsa_circ_254713,RMVar_hsa_circ_254711,RMVar_hsa_circ_102318,RMVar_hsa_circ_118455,RMVar_hsa_circ_116780,RMVar_hsa_circ_254720,RMVar_hsa_circ_254718,RMVar_hsa_circ_254719,RMVar_hsa_circ_79843,RMVar_hsa_circ_301995,RMVar_hsa_circ_345993,RMVar_hsa_circ_293517,RMVar_hsa_circ_50439,RMVar_hsa_circ_68510,RMVar_hsa_circ_34510,RMVar_hsa_circ_19337,RMVar_hsa_circ_36824,RMVar_hsa_circ_46062,RMVar_hsa_circ_254724,RMVar_hsa_circ_14253,RMVar_hsa_circ_254723,RMVar_hsa_circ_364371,RMVar_hsa_circ_342408,RMVar_hsa_circ_329586,RMVar_hsa_circ_312100,RMVar_hsa_circ_271231,RMVar_hsa_circ_270866,RMVar_hsa_circ_291797,RMVar_hsa_circ_335902,RMVar_hsa_circ_254726,RMVar_hsa_circ_376365,RMVar_hsa_circ_254725,RMVar_hsa_circ_378315,RMVar_hsa_circ_339697,RMVar_hsa_circ_298567,RMVar_hsa_circ_52177,RMVar_hsa_circ_270177,RMVar_hsa_circ_42162,RMVar_hsa_circ_254730,RMVar_hsa_circ_254732,RMVar_hsa_circ_254733,RMVar_hsa_circ_254734,RMVar_hsa_circ_254731,RMVar_hsa_circ_293992,RMVar_hsa_circ_311115,RMVar_hsa_circ_363588,RMVar_hsa_circ_298473,RMVar_hsa_circ_40870,RMVar_hsa_circ_54342,RMVar_hsa_circ_63759,RMVar_hsa_circ_254735,RMVar_hsa_circ_254737,RMVar_hsa_circ_254738,RMVar_hsa_circ_254736,RMVar_hsa_circ_254741,RMVar_hsa_circ_75783,RMVar_hsa_circ_77007,RMVar_hsa_circ_26426,RMVar_hsa_circ_332185,RMVar_hsa_circ_254740,RMVar_hsa_circ_340154,RMVar_hsa_circ_284585,RMVar_hsa_circ_48382,RMVar_hsa_circ_254742 10303 RMVar_ID_10303 Human_SNP_ID_385192801 A-to-I Human chr8 - 140775623 140775623 140775623 ATAAAAATCAAGGGCCTGGTATGGTGGCTCACACCTATAGTCCCAGCACTTCAGGGAGGCCGAGG ATAAAAATCAAGGGCCTGGTATGGTGGCTCACCCCTATAGTCCCAGCACTTCAGGGAGGCCGAGG T G PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1288908519 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_99024,RMVar_hsa_circ_119341,RMVar_hsa_circ_89446,RMVar_hsa_circ_9428,RMVar_hsa_circ_254699,RMVar_hsa_circ_254700,RMVar_hsa_circ_254698,RMVar_hsa_circ_63815,RMVar_hsa_circ_6314,RMVar_hsa_circ_254703,RMVar_hsa_circ_120136,RMVar_hsa_circ_108356,RMVar_hsa_circ_85561,RMVar_hsa_circ_355294,RMVar_hsa_circ_254707,RMVar_hsa_circ_334369,RMVar_hsa_circ_103169,RMVar_hsa_circ_62254,RMVar_hsa_circ_43746,RMVar_hsa_circ_254708,RMVar_hsa_circ_254709,RMVar_hsa_circ_355189,RMVar_hsa_circ_372200,RMVar_hsa_circ_324678,RMVar_hsa_circ_322054,RMVar_hsa_circ_100311,RMVar_hsa_circ_55128,RMVar_hsa_circ_62919,RMVar_hsa_circ_254710,RMVar_hsa_circ_254711,RMVar_hsa_circ_102318,RMVar_hsa_circ_116780,RMVar_hsa_circ_254720,RMVar_hsa_circ_254719,RMVar_hsa_circ_79843,RMVar_hsa_circ_293517,RMVar_hsa_circ_50439,RMVar_hsa_circ_68510,RMVar_hsa_circ_34510,RMVar_hsa_circ_2596,RMVar_hsa_circ_36824,RMVar_hsa_circ_46062,RMVar_hsa_circ_254724,RMVar_hsa_circ_14253,RMVar_hsa_circ_364371,RMVar_hsa_circ_342408,RMVar_hsa_circ_329586,RMVar_hsa_circ_271231,RMVar_hsa_circ_335902,RMVar_hsa_circ_376365,RMVar_hsa_circ_378315,RMVar_hsa_circ_298567,RMVar_hsa_circ_52177,RMVar_hsa_circ_270177,RMVar_hsa_circ_42162,RMVar_hsa_circ_254732,RMVar_hsa_circ_254733,RMVar_hsa_circ_254734,RMVar_hsa_circ_254731,RMVar_hsa_circ_363588,RMVar_hsa_circ_54342,RMVar_hsa_circ_63759,RMVar_hsa_circ_254735,RMVar_hsa_circ_254741,RMVar_hsa_circ_75783,RMVar_hsa_circ_77007,RMVar_hsa_circ_254740,RMVar_hsa_circ_299952,RMVar_hsa_circ_34776,RMVar_hsa_circ_86359,RMVar_hsa_circ_48382,RMVar_hsa_circ_362415,RMVar_hsa_circ_254743,RMVar_hsa_circ_366700,RMVar_hsa_circ_286767,RMVar_hsa_circ_305313,RMVar_hsa_circ_70995,RMVar_hsa_circ_254745,RMVar_hsa_circ_254746,RMVar_hsa_circ_347300,RMVar_hsa_circ_349832,RMVar_hsa_circ_254744,RMVar_hsa_circ_347878,RMVar_hsa_circ_332346,RMVar_hsa_circ_293009,RMVar_hsa_circ_299884,RMVar_hsa_circ_294257,RMVar_hsa_circ_288942,RMVar_hsa_circ_19264,RMVar_hsa_circ_254752,RMVar_hsa_circ_254754,RMVar_hsa_circ_254755,RMVar_hsa_circ_254756,RMVar_hsa_circ_254753,RMVar_hsa_circ_254751,RMVar_hsa_circ_50049,RMVar_hsa_circ_349698,RMVar_hsa_circ_354635 10304 RMVar_ID_10304 Human_SNP_ID_385192932 A-to-I Human chr8 - 140776141 140776141 140776141 AAATTAACCAGGTGTGGTGGCGGATGCCTGTAATCCCAGCCACTGGGGAGGCTTAGGCACGAGAA AAATTAACCAGGTGTGGTGGCGGATGCCTGTATTCCCAGCCACTGGGGAGGCTTAGGCACGAGAA T A PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs532930434 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_99024,RMVar_hsa_circ_119341,RMVar_hsa_circ_89446,RMVar_hsa_circ_9428,RMVar_hsa_circ_254699,RMVar_hsa_circ_254700,RMVar_hsa_circ_254698,RMVar_hsa_circ_63815,RMVar_hsa_circ_6314,RMVar_hsa_circ_254703,RMVar_hsa_circ_120136,RMVar_hsa_circ_108356,RMVar_hsa_circ_85561,RMVar_hsa_circ_355294,RMVar_hsa_circ_254707,RMVar_hsa_circ_334369,RMVar_hsa_circ_103169,RMVar_hsa_circ_62254,RMVar_hsa_circ_43746,RMVar_hsa_circ_254708,RMVar_hsa_circ_254709,RMVar_hsa_circ_355189,RMVar_hsa_circ_372200,RMVar_hsa_circ_324678,RMVar_hsa_circ_322054,RMVar_hsa_circ_100311,RMVar_hsa_circ_55128,RMVar_hsa_circ_62919,RMVar_hsa_circ_254710,RMVar_hsa_circ_254711,RMVar_hsa_circ_102318,RMVar_hsa_circ_116780,RMVar_hsa_circ_254720,RMVar_hsa_circ_254719,RMVar_hsa_circ_79843,RMVar_hsa_circ_293517,RMVar_hsa_circ_50439,RMVar_hsa_circ_68510,RMVar_hsa_circ_34510,RMVar_hsa_circ_2596,RMVar_hsa_circ_36824,RMVar_hsa_circ_46062,RMVar_hsa_circ_254724,RMVar_hsa_circ_14253,RMVar_hsa_circ_364371,RMVar_hsa_circ_342408,RMVar_hsa_circ_329586,RMVar_hsa_circ_271231,RMVar_hsa_circ_335902,RMVar_hsa_circ_376365,RMVar_hsa_circ_378315,RMVar_hsa_circ_298567,RMVar_hsa_circ_52177,RMVar_hsa_circ_270177,RMVar_hsa_circ_42162,RMVar_hsa_circ_254732,RMVar_hsa_circ_254733,RMVar_hsa_circ_254734,RMVar_hsa_circ_254731,RMVar_hsa_circ_363588,RMVar_hsa_circ_54342,RMVar_hsa_circ_63759,RMVar_hsa_circ_254735,RMVar_hsa_circ_254741,RMVar_hsa_circ_75783,RMVar_hsa_circ_77007,RMVar_hsa_circ_254740,RMVar_hsa_circ_299952,RMVar_hsa_circ_34776,RMVar_hsa_circ_86359,RMVar_hsa_circ_48382,RMVar_hsa_circ_362415,RMVar_hsa_circ_254743,RMVar_hsa_circ_366700,RMVar_hsa_circ_286767,RMVar_hsa_circ_305313,RMVar_hsa_circ_70995,RMVar_hsa_circ_254745,RMVar_hsa_circ_254746,RMVar_hsa_circ_347300,RMVar_hsa_circ_349832,RMVar_hsa_circ_254744,RMVar_hsa_circ_347878,RMVar_hsa_circ_332346,RMVar_hsa_circ_293009,RMVar_hsa_circ_299884,RMVar_hsa_circ_294257,RMVar_hsa_circ_288942,RMVar_hsa_circ_19264,RMVar_hsa_circ_254752,RMVar_hsa_circ_254754,RMVar_hsa_circ_254755,RMVar_hsa_circ_254756,RMVar_hsa_circ_254753,RMVar_hsa_circ_254751,RMVar_hsa_circ_50049,RMVar_hsa_circ_349698,RMVar_hsa_circ_354635 10305 RMVar_ID_10305 Human_SNP_ID_385192933 A-to-I Human chr8 - 140776141 140776141 140776141 AAATTAACCAGGTGTGGTGGCGGATGCCTGTAATCCCAGCCACTGGGGAGGCTTAGGCACGAGAA AAATTAACCAGGTGTGGTGGCGGATGCCTGTAGTCCCAGCCACTGGGGAGGCTTAGGCACGAGAA T C PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs532930434 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_99024,RMVar_hsa_circ_119341,RMVar_hsa_circ_89446,RMVar_hsa_circ_9428,RMVar_hsa_circ_254699,RMVar_hsa_circ_254700,RMVar_hsa_circ_254698,RMVar_hsa_circ_63815,RMVar_hsa_circ_6314,RMVar_hsa_circ_254703,RMVar_hsa_circ_120136,RMVar_hsa_circ_108356,RMVar_hsa_circ_85561,RMVar_hsa_circ_355294,RMVar_hsa_circ_254707,RMVar_hsa_circ_334369,RMVar_hsa_circ_103169,RMVar_hsa_circ_62254,RMVar_hsa_circ_43746,RMVar_hsa_circ_254708,RMVar_hsa_circ_254709,RMVar_hsa_circ_355189,RMVar_hsa_circ_372200,RMVar_hsa_circ_324678,RMVar_hsa_circ_322054,RMVar_hsa_circ_100311,RMVar_hsa_circ_55128,RMVar_hsa_circ_62919,RMVar_hsa_circ_254710,RMVar_hsa_circ_254711,RMVar_hsa_circ_102318,RMVar_hsa_circ_116780,RMVar_hsa_circ_254720,RMVar_hsa_circ_254719,RMVar_hsa_circ_79843,RMVar_hsa_circ_293517,RMVar_hsa_circ_50439,RMVar_hsa_circ_68510,RMVar_hsa_circ_34510,RMVar_hsa_circ_2596,RMVar_hsa_circ_36824,RMVar_hsa_circ_46062,RMVar_hsa_circ_254724,RMVar_hsa_circ_14253,RMVar_hsa_circ_364371,RMVar_hsa_circ_342408,RMVar_hsa_circ_329586,RMVar_hsa_circ_271231,RMVar_hsa_circ_335902,RMVar_hsa_circ_376365,RMVar_hsa_circ_378315,RMVar_hsa_circ_298567,RMVar_hsa_circ_52177,RMVar_hsa_circ_270177,RMVar_hsa_circ_42162,RMVar_hsa_circ_254732,RMVar_hsa_circ_254733,RMVar_hsa_circ_254734,RMVar_hsa_circ_254731,RMVar_hsa_circ_363588,RMVar_hsa_circ_54342,RMVar_hsa_circ_63759,RMVar_hsa_circ_254735,RMVar_hsa_circ_254741,RMVar_hsa_circ_75783,RMVar_hsa_circ_77007,RMVar_hsa_circ_254740,RMVar_hsa_circ_299952,RMVar_hsa_circ_34776,RMVar_hsa_circ_86359,RMVar_hsa_circ_48382,RMVar_hsa_circ_362415,RMVar_hsa_circ_254743,RMVar_hsa_circ_366700,RMVar_hsa_circ_286767,RMVar_hsa_circ_305313,RMVar_hsa_circ_70995,RMVar_hsa_circ_254745,RMVar_hsa_circ_254746,RMVar_hsa_circ_347300,RMVar_hsa_circ_349832,RMVar_hsa_circ_254744,RMVar_hsa_circ_347878,RMVar_hsa_circ_332346,RMVar_hsa_circ_293009,RMVar_hsa_circ_299884,RMVar_hsa_circ_294257,RMVar_hsa_circ_288942,RMVar_hsa_circ_19264,RMVar_hsa_circ_254752,RMVar_hsa_circ_254754,RMVar_hsa_circ_254755,RMVar_hsa_circ_254756,RMVar_hsa_circ_254753,RMVar_hsa_circ_254751,RMVar_hsa_circ_50049,RMVar_hsa_circ_349698,RMVar_hsa_circ_354635 10306 RMVar_ID_10306 Human_SNP_ID_385203532 A-to-I Human chr8 - 140820118 140820088 140820119 TCCAGTCTGGGCGACAGAGTGAGACCCTATTTAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA TCCAGTCTGGGCGACAGAGTGAGACCCTATT_______________________________AAA TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTA T PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1436532317 Functional Loss DEL dbSNP153 32..62 33 - - - RMVar_hsa_circ_101087,RMVar_hsa_circ_254695,RMVar_hsa_circ_119341,RMVar_hsa_circ_9428,RMVar_hsa_circ_254700,RMVar_hsa_circ_63815,RMVar_hsa_circ_6314,RMVar_hsa_circ_254703,RMVar_hsa_circ_120136,RMVar_hsa_circ_108356,RMVar_hsa_circ_355294,RMVar_hsa_circ_254707,RMVar_hsa_circ_334369,RMVar_hsa_circ_103169,RMVar_hsa_circ_62254,RMVar_hsa_circ_43746,RMVar_hsa_circ_254709,RMVar_hsa_circ_355189,RMVar_hsa_circ_372200,RMVar_hsa_circ_324678,RMVar_hsa_circ_322054,RMVar_hsa_circ_100311,RMVar_hsa_circ_55128,RMVar_hsa_circ_254710,RMVar_hsa_circ_254711,RMVar_hsa_circ_254720,RMVar_hsa_circ_79843,RMVar_hsa_circ_293517,RMVar_hsa_circ_50439,RMVar_hsa_circ_34510,RMVar_hsa_circ_16409,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_54342,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_254745,RMVar_hsa_circ_349832,RMVar_hsa_circ_254744,RMVar_hsa_circ_347878,RMVar_hsa_circ_332346,RMVar_hsa_circ_294257,RMVar_hsa_circ_288942,RMVar_hsa_circ_19264,RMVar_hsa_circ_254757,RMVar_hsa_circ_87603,RMVar_hsa_circ_312922,RMVar_hsa_circ_254755,RMVar_hsa_circ_254756,RMVar_hsa_circ_50049,RMVar_hsa_circ_349698,RMVar_hsa_circ_313275,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_254763,RMVar_hsa_circ_254764,RMVar_hsa_circ_254762,RMVar_hsa_circ_254759,RMVar_hsa_circ_254760,RMVar_hsa_circ_254758,RMVar_hsa_circ_254775,RMVar_hsa_circ_298297,RMVar_hsa_circ_254769,RMVar_hsa_circ_330673,RMVar_hsa_circ_332870,RMVar_hsa_circ_322670,RMVar_hsa_circ_48253,RMVar_hsa_circ_49484,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_292962,RMVar_hsa_circ_275014,RMVar_hsa_circ_254777,RMVar_hsa_circ_254776,RMVar_hsa_circ_28404,RMVar_hsa_circ_5209,RMVar_hsa_circ_254773,RMVar_hsa_circ_254774,RMVar_hsa_circ_280042,RMVar_hsa_circ_348271,RMVar_hsa_circ_344085,RMVar_hsa_circ_282877,RMVar_hsa_circ_254781,RMVar_hsa_circ_298072,RMVar_hsa_circ_319301,RMVar_hsa_circ_293225,RMVar_hsa_circ_283910,RMVar_hsa_circ_273049,RMVar_hsa_circ_280533,RMVar_hsa_circ_53314,RMVar_hsa_circ_254784,RMVar_hsa_circ_254786,RMVar_hsa_circ_254788,RMVar_hsa_circ_21231,RMVar_hsa_circ_254787,RMVar_hsa_circ_254785,RMVar_hsa_circ_254783,RMVar_hsa_circ_93272,RMVar_hsa_circ_254789 10307 RMVar_ID_10307 Human_SNP_ID_385203534 A-to-I Human chr8 - 140820118 140820089 140820119 TCCAGTCTGGGCGACAGAGTGAGACCCTATTTAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA TCCAGTCTGGGCGACAGAGTGAGACCCTATT______________________________AAAA TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTA T PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1168043420 Functional Loss DEL dbSNP153 32..61 33 - - - RMVar_hsa_circ_101087,RMVar_hsa_circ_254695,RMVar_hsa_circ_119341,RMVar_hsa_circ_9428,RMVar_hsa_circ_254700,RMVar_hsa_circ_63815,RMVar_hsa_circ_6314,RMVar_hsa_circ_254703,RMVar_hsa_circ_120136,RMVar_hsa_circ_108356,RMVar_hsa_circ_355294,RMVar_hsa_circ_254707,RMVar_hsa_circ_334369,RMVar_hsa_circ_103169,RMVar_hsa_circ_62254,RMVar_hsa_circ_43746,RMVar_hsa_circ_254709,RMVar_hsa_circ_355189,RMVar_hsa_circ_372200,RMVar_hsa_circ_324678,RMVar_hsa_circ_322054,RMVar_hsa_circ_100311,RMVar_hsa_circ_55128,RMVar_hsa_circ_254710,RMVar_hsa_circ_254711,RMVar_hsa_circ_254720,RMVar_hsa_circ_79843,RMVar_hsa_circ_293517,RMVar_hsa_circ_50439,RMVar_hsa_circ_34510,RMVar_hsa_circ_16409,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_54342,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_254745,RMVar_hsa_circ_349832,RMVar_hsa_circ_254744,RMVar_hsa_circ_347878,RMVar_hsa_circ_332346,RMVar_hsa_circ_294257,RMVar_hsa_circ_288942,RMVar_hsa_circ_19264,RMVar_hsa_circ_254757,RMVar_hsa_circ_87603,RMVar_hsa_circ_312922,RMVar_hsa_circ_254755,RMVar_hsa_circ_254756,RMVar_hsa_circ_50049,RMVar_hsa_circ_349698,RMVar_hsa_circ_313275,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_254763,RMVar_hsa_circ_254764,RMVar_hsa_circ_254762,RMVar_hsa_circ_254759,RMVar_hsa_circ_254760,RMVar_hsa_circ_254758,RMVar_hsa_circ_254775,RMVar_hsa_circ_298297,RMVar_hsa_circ_254769,RMVar_hsa_circ_330673,RMVar_hsa_circ_332870,RMVar_hsa_circ_322670,RMVar_hsa_circ_48253,RMVar_hsa_circ_49484,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_292962,RMVar_hsa_circ_275014,RMVar_hsa_circ_254777,RMVar_hsa_circ_254776,RMVar_hsa_circ_28404,RMVar_hsa_circ_5209,RMVar_hsa_circ_254773,RMVar_hsa_circ_254774,RMVar_hsa_circ_280042,RMVar_hsa_circ_348271,RMVar_hsa_circ_344085,RMVar_hsa_circ_282877,RMVar_hsa_circ_254781,RMVar_hsa_circ_298072,RMVar_hsa_circ_319301,RMVar_hsa_circ_293225,RMVar_hsa_circ_283910,RMVar_hsa_circ_273049,RMVar_hsa_circ_280533,RMVar_hsa_circ_53314,RMVar_hsa_circ_254784,RMVar_hsa_circ_254786,RMVar_hsa_circ_254788,RMVar_hsa_circ_21231,RMVar_hsa_circ_254787,RMVar_hsa_circ_254785,RMVar_hsa_circ_254783,RMVar_hsa_circ_93272,RMVar_hsa_circ_254789 10308 RMVar_ID_10308 Human_SNP_ID_385203535 A-to-I Human chr8 - 140820118 140820090 140820119 TCCAGTCTGGGCGACAGAGTGAGACCCTATTTAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA TCCAGTCTGGGCGACAGAGTGAGACCCTATT_____________________________AAAAA TTTTTTTTTTTTTTTTTTTTTTTTTTTTTA T PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1421901590 Functional Loss DEL dbSNP153 32..60 33 - - - RMVar_hsa_circ_101087,RMVar_hsa_circ_254695,RMVar_hsa_circ_119341,RMVar_hsa_circ_9428,RMVar_hsa_circ_254700,RMVar_hsa_circ_63815,RMVar_hsa_circ_6314,RMVar_hsa_circ_254703,RMVar_hsa_circ_120136,RMVar_hsa_circ_108356,RMVar_hsa_circ_355294,RMVar_hsa_circ_254707,RMVar_hsa_circ_334369,RMVar_hsa_circ_103169,RMVar_hsa_circ_62254,RMVar_hsa_circ_43746,RMVar_hsa_circ_254709,RMVar_hsa_circ_355189,RMVar_hsa_circ_372200,RMVar_hsa_circ_324678,RMVar_hsa_circ_322054,RMVar_hsa_circ_100311,RMVar_hsa_circ_55128,RMVar_hsa_circ_254710,RMVar_hsa_circ_254711,RMVar_hsa_circ_254720,RMVar_hsa_circ_79843,RMVar_hsa_circ_293517,RMVar_hsa_circ_50439,RMVar_hsa_circ_34510,RMVar_hsa_circ_16409,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_54342,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_254745,RMVar_hsa_circ_349832,RMVar_hsa_circ_254744,RMVar_hsa_circ_347878,RMVar_hsa_circ_332346,RMVar_hsa_circ_294257,RMVar_hsa_circ_288942,RMVar_hsa_circ_19264,RMVar_hsa_circ_254757,RMVar_hsa_circ_87603,RMVar_hsa_circ_312922,RMVar_hsa_circ_254755,RMVar_hsa_circ_254756,RMVar_hsa_circ_50049,RMVar_hsa_circ_349698,RMVar_hsa_circ_313275,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_254763,RMVar_hsa_circ_254764,RMVar_hsa_circ_254762,RMVar_hsa_circ_254759,RMVar_hsa_circ_254760,RMVar_hsa_circ_254758,RMVar_hsa_circ_254775,RMVar_hsa_circ_298297,RMVar_hsa_circ_254769,RMVar_hsa_circ_330673,RMVar_hsa_circ_332870,RMVar_hsa_circ_322670,RMVar_hsa_circ_48253,RMVar_hsa_circ_49484,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_292962,RMVar_hsa_circ_275014,RMVar_hsa_circ_254777,RMVar_hsa_circ_254776,RMVar_hsa_circ_28404,RMVar_hsa_circ_5209,RMVar_hsa_circ_254773,RMVar_hsa_circ_254774,RMVar_hsa_circ_280042,RMVar_hsa_circ_348271,RMVar_hsa_circ_344085,RMVar_hsa_circ_282877,RMVar_hsa_circ_254781,RMVar_hsa_circ_298072,RMVar_hsa_circ_319301,RMVar_hsa_circ_293225,RMVar_hsa_circ_283910,RMVar_hsa_circ_273049,RMVar_hsa_circ_280533,RMVar_hsa_circ_53314,RMVar_hsa_circ_254784,RMVar_hsa_circ_254786,RMVar_hsa_circ_254788,RMVar_hsa_circ_21231,RMVar_hsa_circ_254787,RMVar_hsa_circ_254785,RMVar_hsa_circ_254783,RMVar_hsa_circ_93272,RMVar_hsa_circ_254789 10309 RMVar_ID_10309 Human_SNP_ID_385203538 A-to-I Human chr8 - 140820118 140820091 140820119 TCCAGTCTGGGCGACAGAGTGAGACCCTATTTAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA TCCAGTCTGGGCGACAGAGTGAGACCCTATT____________________________AAAAAA TTTTTTTTTTTTTTTTTTTTTTTTTTTTA T PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1483104897 Functional Loss DEL dbSNP153 32..59 33 - - - RMVar_hsa_circ_101087,RMVar_hsa_circ_254695,RMVar_hsa_circ_119341,RMVar_hsa_circ_9428,RMVar_hsa_circ_254700,RMVar_hsa_circ_63815,RMVar_hsa_circ_6314,RMVar_hsa_circ_254703,RMVar_hsa_circ_120136,RMVar_hsa_circ_108356,RMVar_hsa_circ_355294,RMVar_hsa_circ_254707,RMVar_hsa_circ_334369,RMVar_hsa_circ_103169,RMVar_hsa_circ_62254,RMVar_hsa_circ_43746,RMVar_hsa_circ_254709,RMVar_hsa_circ_355189,RMVar_hsa_circ_372200,RMVar_hsa_circ_324678,RMVar_hsa_circ_322054,RMVar_hsa_circ_100311,RMVar_hsa_circ_55128,RMVar_hsa_circ_254710,RMVar_hsa_circ_254711,RMVar_hsa_circ_254720,RMVar_hsa_circ_79843,RMVar_hsa_circ_293517,RMVar_hsa_circ_50439,RMVar_hsa_circ_34510,RMVar_hsa_circ_16409,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_54342,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_254745,RMVar_hsa_circ_349832,RMVar_hsa_circ_254744,RMVar_hsa_circ_347878,RMVar_hsa_circ_332346,RMVar_hsa_circ_294257,RMVar_hsa_circ_288942,RMVar_hsa_circ_19264,RMVar_hsa_circ_254757,RMVar_hsa_circ_87603,RMVar_hsa_circ_312922,RMVar_hsa_circ_254755,RMVar_hsa_circ_254756,RMVar_hsa_circ_50049,RMVar_hsa_circ_349698,RMVar_hsa_circ_313275,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_254763,RMVar_hsa_circ_254764,RMVar_hsa_circ_254762,RMVar_hsa_circ_254759,RMVar_hsa_circ_254760,RMVar_hsa_circ_254758,RMVar_hsa_circ_254775,RMVar_hsa_circ_298297,RMVar_hsa_circ_254769,RMVar_hsa_circ_330673,RMVar_hsa_circ_332870,RMVar_hsa_circ_322670,RMVar_hsa_circ_48253,RMVar_hsa_circ_49484,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_292962,RMVar_hsa_circ_275014,RMVar_hsa_circ_254777,RMVar_hsa_circ_254776,RMVar_hsa_circ_28404,RMVar_hsa_circ_5209,RMVar_hsa_circ_254773,RMVar_hsa_circ_254774,RMVar_hsa_circ_280042,RMVar_hsa_circ_348271,RMVar_hsa_circ_344085,RMVar_hsa_circ_282877,RMVar_hsa_circ_254781,RMVar_hsa_circ_298072,RMVar_hsa_circ_319301,RMVar_hsa_circ_293225,RMVar_hsa_circ_283910,RMVar_hsa_circ_273049,RMVar_hsa_circ_280533,RMVar_hsa_circ_53314,RMVar_hsa_circ_254784,RMVar_hsa_circ_254786,RMVar_hsa_circ_254788,RMVar_hsa_circ_21231,RMVar_hsa_circ_254787,RMVar_hsa_circ_254785,RMVar_hsa_circ_254783,RMVar_hsa_circ_93272,RMVar_hsa_circ_254789 10310 RMVar_ID_10310 Human_SNP_ID_385203539 A-to-I Human chr8 - 140820118 140820092 140820119 TCCAGTCTGGGCGACAGAGTGAGACCCTATTTAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA TCCAGTCTGGGCGACAGAGTGAGACCCTATT___________________________AAAAAAA TTTTTTTTTTTTTTTTTTTTTTTTTTTA T PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1420755177 Functional Loss DEL dbSNP153 32..58 33 - - - RMVar_hsa_circ_101087,RMVar_hsa_circ_254695,RMVar_hsa_circ_119341,RMVar_hsa_circ_9428,RMVar_hsa_circ_254700,RMVar_hsa_circ_63815,RMVar_hsa_circ_6314,RMVar_hsa_circ_254703,RMVar_hsa_circ_120136,RMVar_hsa_circ_108356,RMVar_hsa_circ_355294,RMVar_hsa_circ_254707,RMVar_hsa_circ_334369,RMVar_hsa_circ_103169,RMVar_hsa_circ_62254,RMVar_hsa_circ_43746,RMVar_hsa_circ_254709,RMVar_hsa_circ_355189,RMVar_hsa_circ_372200,RMVar_hsa_circ_324678,RMVar_hsa_circ_322054,RMVar_hsa_circ_100311,RMVar_hsa_circ_55128,RMVar_hsa_circ_254710,RMVar_hsa_circ_254711,RMVar_hsa_circ_254720,RMVar_hsa_circ_79843,RMVar_hsa_circ_293517,RMVar_hsa_circ_50439,RMVar_hsa_circ_34510,RMVar_hsa_circ_16409,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_54342,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_254745,RMVar_hsa_circ_349832,RMVar_hsa_circ_254744,RMVar_hsa_circ_347878,RMVar_hsa_circ_332346,RMVar_hsa_circ_294257,RMVar_hsa_circ_288942,RMVar_hsa_circ_19264,RMVar_hsa_circ_254757,RMVar_hsa_circ_87603,RMVar_hsa_circ_312922,RMVar_hsa_circ_254755,RMVar_hsa_circ_254756,RMVar_hsa_circ_50049,RMVar_hsa_circ_349698,RMVar_hsa_circ_313275,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_254763,RMVar_hsa_circ_254764,RMVar_hsa_circ_254762,RMVar_hsa_circ_254759,RMVar_hsa_circ_254760,RMVar_hsa_circ_254758,RMVar_hsa_circ_254775,RMVar_hsa_circ_298297,RMVar_hsa_circ_254769,RMVar_hsa_circ_330673,RMVar_hsa_circ_332870,RMVar_hsa_circ_322670,RMVar_hsa_circ_48253,RMVar_hsa_circ_49484,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_292962,RMVar_hsa_circ_275014,RMVar_hsa_circ_254777,RMVar_hsa_circ_254776,RMVar_hsa_circ_28404,RMVar_hsa_circ_5209,RMVar_hsa_circ_254773,RMVar_hsa_circ_254774,RMVar_hsa_circ_280042,RMVar_hsa_circ_348271,RMVar_hsa_circ_344085,RMVar_hsa_circ_282877,RMVar_hsa_circ_254781,RMVar_hsa_circ_298072,RMVar_hsa_circ_319301,RMVar_hsa_circ_293225,RMVar_hsa_circ_283910,RMVar_hsa_circ_273049,RMVar_hsa_circ_280533,RMVar_hsa_circ_53314,RMVar_hsa_circ_254784,RMVar_hsa_circ_254786,RMVar_hsa_circ_254788,RMVar_hsa_circ_21231,RMVar_hsa_circ_254787,RMVar_hsa_circ_254785,RMVar_hsa_circ_254783,RMVar_hsa_circ_93272,RMVar_hsa_circ_254789 10311 RMVar_ID_10311 Human_SNP_ID_385203540 A-to-I Human chr8 - 140820118 140820093 140820119 TCCAGTCTGGGCGACAGAGTGAGACCCTATTTAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA TCCAGTCTGGGCGACAGAGTGAGACCCTATT__________________________AAAAAAAA TTTTTTTTTTTTTTTTTTTTTTTTTTA T PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1300414093 Functional Loss DEL dbSNP153 32..57 33 - - - RMVar_hsa_circ_101087,RMVar_hsa_circ_254695,RMVar_hsa_circ_119341,RMVar_hsa_circ_9428,RMVar_hsa_circ_254700,RMVar_hsa_circ_63815,RMVar_hsa_circ_6314,RMVar_hsa_circ_254703,RMVar_hsa_circ_120136,RMVar_hsa_circ_108356,RMVar_hsa_circ_355294,RMVar_hsa_circ_254707,RMVar_hsa_circ_334369,RMVar_hsa_circ_103169,RMVar_hsa_circ_62254,RMVar_hsa_circ_43746,RMVar_hsa_circ_254709,RMVar_hsa_circ_355189,RMVar_hsa_circ_372200,RMVar_hsa_circ_324678,RMVar_hsa_circ_322054,RMVar_hsa_circ_100311,RMVar_hsa_circ_55128,RMVar_hsa_circ_254710,RMVar_hsa_circ_254711,RMVar_hsa_circ_254720,RMVar_hsa_circ_79843,RMVar_hsa_circ_293517,RMVar_hsa_circ_50439,RMVar_hsa_circ_34510,RMVar_hsa_circ_16409,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_54342,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_254745,RMVar_hsa_circ_349832,RMVar_hsa_circ_254744,RMVar_hsa_circ_347878,RMVar_hsa_circ_332346,RMVar_hsa_circ_294257,RMVar_hsa_circ_288942,RMVar_hsa_circ_19264,RMVar_hsa_circ_254757,RMVar_hsa_circ_87603,RMVar_hsa_circ_312922,RMVar_hsa_circ_254755,RMVar_hsa_circ_254756,RMVar_hsa_circ_50049,RMVar_hsa_circ_349698,RMVar_hsa_circ_313275,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_254763,RMVar_hsa_circ_254764,RMVar_hsa_circ_254762,RMVar_hsa_circ_254759,RMVar_hsa_circ_254760,RMVar_hsa_circ_254758,RMVar_hsa_circ_254775,RMVar_hsa_circ_298297,RMVar_hsa_circ_254769,RMVar_hsa_circ_330673,RMVar_hsa_circ_332870,RMVar_hsa_circ_322670,RMVar_hsa_circ_48253,RMVar_hsa_circ_49484,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_292962,RMVar_hsa_circ_275014,RMVar_hsa_circ_254777,RMVar_hsa_circ_254776,RMVar_hsa_circ_28404,RMVar_hsa_circ_5209,RMVar_hsa_circ_254773,RMVar_hsa_circ_254774,RMVar_hsa_circ_280042,RMVar_hsa_circ_348271,RMVar_hsa_circ_344085,RMVar_hsa_circ_282877,RMVar_hsa_circ_254781,RMVar_hsa_circ_298072,RMVar_hsa_circ_319301,RMVar_hsa_circ_293225,RMVar_hsa_circ_283910,RMVar_hsa_circ_273049,RMVar_hsa_circ_280533,RMVar_hsa_circ_53314,RMVar_hsa_circ_254784,RMVar_hsa_circ_254786,RMVar_hsa_circ_254788,RMVar_hsa_circ_21231,RMVar_hsa_circ_254787,RMVar_hsa_circ_254785,RMVar_hsa_circ_254783,RMVar_hsa_circ_93272,RMVar_hsa_circ_254789 10312 RMVar_ID_10312 Human_SNP_ID_385203542 A-to-I Human chr8 - 140820118 140820094 140820119 TCCAGTCTGGGCGACAGAGTGAGACCCTATTTAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA TCCAGTCTGGGCGACAGAGTGAGACCCTATT_________________________AAAAAAAAA TTTTTTTTTTTTTTTTTTTTTTTTTA T PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1363977426 Functional Loss DEL dbSNP153 32..56 33 - - - RMVar_hsa_circ_101087,RMVar_hsa_circ_254695,RMVar_hsa_circ_119341,RMVar_hsa_circ_9428,RMVar_hsa_circ_254700,RMVar_hsa_circ_63815,RMVar_hsa_circ_6314,RMVar_hsa_circ_254703,RMVar_hsa_circ_120136,RMVar_hsa_circ_108356,RMVar_hsa_circ_355294,RMVar_hsa_circ_254707,RMVar_hsa_circ_334369,RMVar_hsa_circ_103169,RMVar_hsa_circ_62254,RMVar_hsa_circ_43746,RMVar_hsa_circ_254709,RMVar_hsa_circ_355189,RMVar_hsa_circ_372200,RMVar_hsa_circ_324678,RMVar_hsa_circ_322054,RMVar_hsa_circ_100311,RMVar_hsa_circ_55128,RMVar_hsa_circ_254710,RMVar_hsa_circ_254711,RMVar_hsa_circ_254720,RMVar_hsa_circ_79843,RMVar_hsa_circ_293517,RMVar_hsa_circ_50439,RMVar_hsa_circ_34510,RMVar_hsa_circ_16409,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_54342,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_254745,RMVar_hsa_circ_349832,RMVar_hsa_circ_254744,RMVar_hsa_circ_347878,RMVar_hsa_circ_332346,RMVar_hsa_circ_294257,RMVar_hsa_circ_288942,RMVar_hsa_circ_19264,RMVar_hsa_circ_254757,RMVar_hsa_circ_87603,RMVar_hsa_circ_312922,RMVar_hsa_circ_254755,RMVar_hsa_circ_254756,RMVar_hsa_circ_50049,RMVar_hsa_circ_349698,RMVar_hsa_circ_313275,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_254763,RMVar_hsa_circ_254764,RMVar_hsa_circ_254762,RMVar_hsa_circ_254759,RMVar_hsa_circ_254760,RMVar_hsa_circ_254758,RMVar_hsa_circ_254775,RMVar_hsa_circ_298297,RMVar_hsa_circ_254769,RMVar_hsa_circ_330673,RMVar_hsa_circ_332870,RMVar_hsa_circ_322670,RMVar_hsa_circ_48253,RMVar_hsa_circ_49484,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_292962,RMVar_hsa_circ_275014,RMVar_hsa_circ_254777,RMVar_hsa_circ_254776,RMVar_hsa_circ_28404,RMVar_hsa_circ_5209,RMVar_hsa_circ_254773,RMVar_hsa_circ_254774,RMVar_hsa_circ_280042,RMVar_hsa_circ_348271,RMVar_hsa_circ_344085,RMVar_hsa_circ_282877,RMVar_hsa_circ_254781,RMVar_hsa_circ_298072,RMVar_hsa_circ_319301,RMVar_hsa_circ_293225,RMVar_hsa_circ_283910,RMVar_hsa_circ_273049,RMVar_hsa_circ_280533,RMVar_hsa_circ_53314,RMVar_hsa_circ_254784,RMVar_hsa_circ_254786,RMVar_hsa_circ_254788,RMVar_hsa_circ_21231,RMVar_hsa_circ_254787,RMVar_hsa_circ_254785,RMVar_hsa_circ_254783,RMVar_hsa_circ_93272,RMVar_hsa_circ_254789 10313 RMVar_ID_10313 Human_SNP_ID_385203544 A-to-I Human chr8 - 140820118 140820095 140820119 TCCAGTCTGGGCGACAGAGTGAGACCCTATTTAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA TCCAGTCTGGGCGACAGAGTGAGACCCTATT________________________AAAAAAAAAA TTTTTTTTTTTTTTTTTTTTTTTTA T PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1307618233 Functional Loss DEL dbSNP153 32..55 33 - - - RMVar_hsa_circ_101087,RMVar_hsa_circ_254695,RMVar_hsa_circ_119341,RMVar_hsa_circ_9428,RMVar_hsa_circ_254700,RMVar_hsa_circ_63815,RMVar_hsa_circ_6314,RMVar_hsa_circ_254703,RMVar_hsa_circ_120136,RMVar_hsa_circ_108356,RMVar_hsa_circ_355294,RMVar_hsa_circ_254707,RMVar_hsa_circ_334369,RMVar_hsa_circ_103169,RMVar_hsa_circ_62254,RMVar_hsa_circ_43746,RMVar_hsa_circ_254709,RMVar_hsa_circ_355189,RMVar_hsa_circ_372200,RMVar_hsa_circ_324678,RMVar_hsa_circ_322054,RMVar_hsa_circ_100311,RMVar_hsa_circ_55128,RMVar_hsa_circ_254710,RMVar_hsa_circ_254711,RMVar_hsa_circ_254720,RMVar_hsa_circ_79843,RMVar_hsa_circ_293517,RMVar_hsa_circ_50439,RMVar_hsa_circ_34510,RMVar_hsa_circ_16409,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_54342,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_254745,RMVar_hsa_circ_349832,RMVar_hsa_circ_254744,RMVar_hsa_circ_347878,RMVar_hsa_circ_332346,RMVar_hsa_circ_294257,RMVar_hsa_circ_288942,RMVar_hsa_circ_19264,RMVar_hsa_circ_254757,RMVar_hsa_circ_87603,RMVar_hsa_circ_312922,RMVar_hsa_circ_254755,RMVar_hsa_circ_254756,RMVar_hsa_circ_50049,RMVar_hsa_circ_349698,RMVar_hsa_circ_313275,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_254763,RMVar_hsa_circ_254764,RMVar_hsa_circ_254762,RMVar_hsa_circ_254759,RMVar_hsa_circ_254760,RMVar_hsa_circ_254758,RMVar_hsa_circ_254775,RMVar_hsa_circ_298297,RMVar_hsa_circ_254769,RMVar_hsa_circ_330673,RMVar_hsa_circ_332870,RMVar_hsa_circ_322670,RMVar_hsa_circ_48253,RMVar_hsa_circ_49484,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_292962,RMVar_hsa_circ_275014,RMVar_hsa_circ_254777,RMVar_hsa_circ_254776,RMVar_hsa_circ_28404,RMVar_hsa_circ_5209,RMVar_hsa_circ_254773,RMVar_hsa_circ_254774,RMVar_hsa_circ_280042,RMVar_hsa_circ_348271,RMVar_hsa_circ_344085,RMVar_hsa_circ_282877,RMVar_hsa_circ_254781,RMVar_hsa_circ_298072,RMVar_hsa_circ_319301,RMVar_hsa_circ_293225,RMVar_hsa_circ_283910,RMVar_hsa_circ_273049,RMVar_hsa_circ_280533,RMVar_hsa_circ_53314,RMVar_hsa_circ_254784,RMVar_hsa_circ_254786,RMVar_hsa_circ_254788,RMVar_hsa_circ_21231,RMVar_hsa_circ_254787,RMVar_hsa_circ_254785,RMVar_hsa_circ_254783,RMVar_hsa_circ_93272,RMVar_hsa_circ_254789 10314 RMVar_ID_10314 Human_SNP_ID_385203546 A-to-I Human chr8 - 140820118 140820096 140820119 TCCAGTCTGGGCGACAGAGTGAGACCCTATTTAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA TCCAGTCTGGGCGACAGAGTGAGACCCTATT_______________________AAAAAAAAAAA TTTTTTTTTTTTTTTTTTTTTTTA T PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404512777 Functional Loss DEL dbSNP153 32..54 33 - - - RMVar_hsa_circ_101087,RMVar_hsa_circ_254695,RMVar_hsa_circ_119341,RMVar_hsa_circ_9428,RMVar_hsa_circ_254700,RMVar_hsa_circ_63815,RMVar_hsa_circ_6314,RMVar_hsa_circ_254703,RMVar_hsa_circ_120136,RMVar_hsa_circ_108356,RMVar_hsa_circ_355294,RMVar_hsa_circ_254707,RMVar_hsa_circ_334369,RMVar_hsa_circ_103169,RMVar_hsa_circ_62254,RMVar_hsa_circ_43746,RMVar_hsa_circ_254709,RMVar_hsa_circ_355189,RMVar_hsa_circ_372200,RMVar_hsa_circ_324678,RMVar_hsa_circ_322054,RMVar_hsa_circ_100311,RMVar_hsa_circ_55128,RMVar_hsa_circ_254710,RMVar_hsa_circ_254711,RMVar_hsa_circ_254720,RMVar_hsa_circ_79843,RMVar_hsa_circ_293517,RMVar_hsa_circ_50439,RMVar_hsa_circ_34510,RMVar_hsa_circ_16409,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_54342,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_254745,RMVar_hsa_circ_349832,RMVar_hsa_circ_254744,RMVar_hsa_circ_347878,RMVar_hsa_circ_332346,RMVar_hsa_circ_294257,RMVar_hsa_circ_288942,RMVar_hsa_circ_19264,RMVar_hsa_circ_254757,RMVar_hsa_circ_87603,RMVar_hsa_circ_312922,RMVar_hsa_circ_254755,RMVar_hsa_circ_254756,RMVar_hsa_circ_50049,RMVar_hsa_circ_349698,RMVar_hsa_circ_313275,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_254763,RMVar_hsa_circ_254764,RMVar_hsa_circ_254762,RMVar_hsa_circ_254759,RMVar_hsa_circ_254760,RMVar_hsa_circ_254758,RMVar_hsa_circ_254775,RMVar_hsa_circ_298297,RMVar_hsa_circ_254769,RMVar_hsa_circ_330673,RMVar_hsa_circ_332870,RMVar_hsa_circ_322670,RMVar_hsa_circ_48253,RMVar_hsa_circ_49484,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_292962,RMVar_hsa_circ_275014,RMVar_hsa_circ_254777,RMVar_hsa_circ_254776,RMVar_hsa_circ_28404,RMVar_hsa_circ_5209,RMVar_hsa_circ_254773,RMVar_hsa_circ_254774,RMVar_hsa_circ_280042,RMVar_hsa_circ_348271,RMVar_hsa_circ_344085,RMVar_hsa_circ_282877,RMVar_hsa_circ_254781,RMVar_hsa_circ_298072,RMVar_hsa_circ_319301,RMVar_hsa_circ_293225,RMVar_hsa_circ_283910,RMVar_hsa_circ_273049,RMVar_hsa_circ_280533,RMVar_hsa_circ_53314,RMVar_hsa_circ_254784,RMVar_hsa_circ_254786,RMVar_hsa_circ_254788,RMVar_hsa_circ_21231,RMVar_hsa_circ_254787,RMVar_hsa_circ_254785,RMVar_hsa_circ_254783,RMVar_hsa_circ_93272,RMVar_hsa_circ_254789 10315 RMVar_ID_10315 Human_SNP_ID_385203547 A-to-I Human chr8 - 140820118 140820097 140820119 TCCAGTCTGGGCGACAGAGTGAGACCCTATTTAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA TCCAGTCTGGGCGACAGAGTGAGACCCTATT______________________AAAAAAAAAAAA TTTTTTTTTTTTTTTTTTTTTTA T PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1324295803 Functional Loss DEL dbSNP153 32..53 33 - - - RMVar_hsa_circ_101087,RMVar_hsa_circ_254695,RMVar_hsa_circ_119341,RMVar_hsa_circ_9428,RMVar_hsa_circ_254700,RMVar_hsa_circ_63815,RMVar_hsa_circ_6314,RMVar_hsa_circ_254703,RMVar_hsa_circ_120136,RMVar_hsa_circ_108356,RMVar_hsa_circ_355294,RMVar_hsa_circ_254707,RMVar_hsa_circ_334369,RMVar_hsa_circ_103169,RMVar_hsa_circ_62254,RMVar_hsa_circ_43746,RMVar_hsa_circ_254709,RMVar_hsa_circ_355189,RMVar_hsa_circ_372200,RMVar_hsa_circ_324678,RMVar_hsa_circ_322054,RMVar_hsa_circ_100311,RMVar_hsa_circ_55128,RMVar_hsa_circ_254710,RMVar_hsa_circ_254711,RMVar_hsa_circ_254720,RMVar_hsa_circ_79843,RMVar_hsa_circ_293517,RMVar_hsa_circ_50439,RMVar_hsa_circ_34510,RMVar_hsa_circ_16409,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_54342,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_254745,RMVar_hsa_circ_349832,RMVar_hsa_circ_254744,RMVar_hsa_circ_347878,RMVar_hsa_circ_332346,RMVar_hsa_circ_294257,RMVar_hsa_circ_288942,RMVar_hsa_circ_19264,RMVar_hsa_circ_254757,RMVar_hsa_circ_87603,RMVar_hsa_circ_312922,RMVar_hsa_circ_254755,RMVar_hsa_circ_254756,RMVar_hsa_circ_50049,RMVar_hsa_circ_349698,RMVar_hsa_circ_313275,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_254763,RMVar_hsa_circ_254764,RMVar_hsa_circ_254762,RMVar_hsa_circ_254759,RMVar_hsa_circ_254760,RMVar_hsa_circ_254758,RMVar_hsa_circ_254775,RMVar_hsa_circ_298297,RMVar_hsa_circ_254769,RMVar_hsa_circ_330673,RMVar_hsa_circ_332870,RMVar_hsa_circ_322670,RMVar_hsa_circ_48253,RMVar_hsa_circ_49484,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_292962,RMVar_hsa_circ_275014,RMVar_hsa_circ_254777,RMVar_hsa_circ_254776,RMVar_hsa_circ_28404,RMVar_hsa_circ_5209,RMVar_hsa_circ_254773,RMVar_hsa_circ_254774,RMVar_hsa_circ_280042,RMVar_hsa_circ_348271,RMVar_hsa_circ_344085,RMVar_hsa_circ_282877,RMVar_hsa_circ_254781,RMVar_hsa_circ_298072,RMVar_hsa_circ_319301,RMVar_hsa_circ_293225,RMVar_hsa_circ_283910,RMVar_hsa_circ_273049,RMVar_hsa_circ_280533,RMVar_hsa_circ_53314,RMVar_hsa_circ_254784,RMVar_hsa_circ_254786,RMVar_hsa_circ_254788,RMVar_hsa_circ_21231,RMVar_hsa_circ_254787,RMVar_hsa_circ_254785,RMVar_hsa_circ_254783,RMVar_hsa_circ_93272,RMVar_hsa_circ_254789 10316 RMVar_ID_10316 Human_SNP_ID_385203549 A-to-I Human chr8 - 140820118 140820098 140820119 TCCAGTCTGGGCGACAGAGTGAGACCCTATTTAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA TCCAGTCTGGGCGACAGAGTGAGACCCTATT_____________________AAAAAAAAAAAAA TTTTTTTTTTTTTTTTTTTTTA T PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1416470500 Functional Loss DEL dbSNP153 32..52 33 - - - RMVar_hsa_circ_101087,RMVar_hsa_circ_254695,RMVar_hsa_circ_119341,RMVar_hsa_circ_9428,RMVar_hsa_circ_254700,RMVar_hsa_circ_63815,RMVar_hsa_circ_6314,RMVar_hsa_circ_254703,RMVar_hsa_circ_120136,RMVar_hsa_circ_108356,RMVar_hsa_circ_355294,RMVar_hsa_circ_254707,RMVar_hsa_circ_334369,RMVar_hsa_circ_103169,RMVar_hsa_circ_62254,RMVar_hsa_circ_43746,RMVar_hsa_circ_254709,RMVar_hsa_circ_355189,RMVar_hsa_circ_372200,RMVar_hsa_circ_324678,RMVar_hsa_circ_322054,RMVar_hsa_circ_100311,RMVar_hsa_circ_55128,RMVar_hsa_circ_254710,RMVar_hsa_circ_254711,RMVar_hsa_circ_254720,RMVar_hsa_circ_79843,RMVar_hsa_circ_293517,RMVar_hsa_circ_50439,RMVar_hsa_circ_34510,RMVar_hsa_circ_16409,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_54342,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_254745,RMVar_hsa_circ_349832,RMVar_hsa_circ_254744,RMVar_hsa_circ_347878,RMVar_hsa_circ_332346,RMVar_hsa_circ_294257,RMVar_hsa_circ_288942,RMVar_hsa_circ_19264,RMVar_hsa_circ_254757,RMVar_hsa_circ_87603,RMVar_hsa_circ_312922,RMVar_hsa_circ_254755,RMVar_hsa_circ_254756,RMVar_hsa_circ_50049,RMVar_hsa_circ_349698,RMVar_hsa_circ_313275,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_254763,RMVar_hsa_circ_254764,RMVar_hsa_circ_254762,RMVar_hsa_circ_254759,RMVar_hsa_circ_254760,RMVar_hsa_circ_254758,RMVar_hsa_circ_254775,RMVar_hsa_circ_298297,RMVar_hsa_circ_254769,RMVar_hsa_circ_330673,RMVar_hsa_circ_332870,RMVar_hsa_circ_322670,RMVar_hsa_circ_48253,RMVar_hsa_circ_49484,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_292962,RMVar_hsa_circ_275014,RMVar_hsa_circ_254777,RMVar_hsa_circ_254776,RMVar_hsa_circ_28404,RMVar_hsa_circ_5209,RMVar_hsa_circ_254773,RMVar_hsa_circ_254774,RMVar_hsa_circ_280042,RMVar_hsa_circ_348271,RMVar_hsa_circ_344085,RMVar_hsa_circ_282877,RMVar_hsa_circ_254781,RMVar_hsa_circ_298072,RMVar_hsa_circ_319301,RMVar_hsa_circ_293225,RMVar_hsa_circ_283910,RMVar_hsa_circ_273049,RMVar_hsa_circ_280533,RMVar_hsa_circ_53314,RMVar_hsa_circ_254784,RMVar_hsa_circ_254786,RMVar_hsa_circ_254788,RMVar_hsa_circ_21231,RMVar_hsa_circ_254787,RMVar_hsa_circ_254785,RMVar_hsa_circ_254783,RMVar_hsa_circ_93272,RMVar_hsa_circ_254789 10317 RMVar_ID_10317 Human_SNP_ID_385203551 A-to-I Human chr8 - 140820118 140820099 140820119 TCCAGTCTGGGCGACAGAGTGAGACCCTATTTAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA TCCAGTCTGGGCGACAGAGTGAGACCCTATT____________________AAAAAAAAAAAAAA TTTTTTTTTTTTTTTTTTTTA T PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1332838721 Functional Loss DEL dbSNP153 32..51 33 - - - RMVar_hsa_circ_101087,RMVar_hsa_circ_254695,RMVar_hsa_circ_119341,RMVar_hsa_circ_9428,RMVar_hsa_circ_254700,RMVar_hsa_circ_63815,RMVar_hsa_circ_6314,RMVar_hsa_circ_254703,RMVar_hsa_circ_120136,RMVar_hsa_circ_108356,RMVar_hsa_circ_355294,RMVar_hsa_circ_254707,RMVar_hsa_circ_334369,RMVar_hsa_circ_103169,RMVar_hsa_circ_62254,RMVar_hsa_circ_43746,RMVar_hsa_circ_254709,RMVar_hsa_circ_355189,RMVar_hsa_circ_372200,RMVar_hsa_circ_324678,RMVar_hsa_circ_322054,RMVar_hsa_circ_100311,RMVar_hsa_circ_55128,RMVar_hsa_circ_254710,RMVar_hsa_circ_254711,RMVar_hsa_circ_254720,RMVar_hsa_circ_79843,RMVar_hsa_circ_293517,RMVar_hsa_circ_50439,RMVar_hsa_circ_34510,RMVar_hsa_circ_16409,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_54342,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_254745,RMVar_hsa_circ_349832,RMVar_hsa_circ_254744,RMVar_hsa_circ_347878,RMVar_hsa_circ_332346,RMVar_hsa_circ_294257,RMVar_hsa_circ_288942,RMVar_hsa_circ_19264,RMVar_hsa_circ_254757,RMVar_hsa_circ_87603,RMVar_hsa_circ_312922,RMVar_hsa_circ_254755,RMVar_hsa_circ_254756,RMVar_hsa_circ_50049,RMVar_hsa_circ_349698,RMVar_hsa_circ_313275,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_254763,RMVar_hsa_circ_254764,RMVar_hsa_circ_254762,RMVar_hsa_circ_254759,RMVar_hsa_circ_254760,RMVar_hsa_circ_254758,RMVar_hsa_circ_254775,RMVar_hsa_circ_298297,RMVar_hsa_circ_254769,RMVar_hsa_circ_330673,RMVar_hsa_circ_332870,RMVar_hsa_circ_322670,RMVar_hsa_circ_48253,RMVar_hsa_circ_49484,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_292962,RMVar_hsa_circ_275014,RMVar_hsa_circ_254777,RMVar_hsa_circ_254776,RMVar_hsa_circ_28404,RMVar_hsa_circ_5209,RMVar_hsa_circ_254773,RMVar_hsa_circ_254774,RMVar_hsa_circ_280042,RMVar_hsa_circ_348271,RMVar_hsa_circ_344085,RMVar_hsa_circ_282877,RMVar_hsa_circ_254781,RMVar_hsa_circ_298072,RMVar_hsa_circ_319301,RMVar_hsa_circ_293225,RMVar_hsa_circ_283910,RMVar_hsa_circ_273049,RMVar_hsa_circ_280533,RMVar_hsa_circ_53314,RMVar_hsa_circ_254784,RMVar_hsa_circ_254786,RMVar_hsa_circ_254788,RMVar_hsa_circ_21231,RMVar_hsa_circ_254787,RMVar_hsa_circ_254785,RMVar_hsa_circ_254783,RMVar_hsa_circ_93272,RMVar_hsa_circ_254789 10318 RMVar_ID_10318 Human_SNP_ID_385203552 A-to-I Human chr8 - 140820118 140820100 140820119 TCCAGTCTGGGCGACAGAGTGAGACCCTATTTAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA TCCAGTCTGGGCGACAGAGTGAGACCCTATT___________________AAAAAAAAAAAAAAA TTTTTTTTTTTTTTTTTTTA T PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1236963870 Functional Loss DEL dbSNP153 32..50 33 - - - RMVar_hsa_circ_101087,RMVar_hsa_circ_254695,RMVar_hsa_circ_119341,RMVar_hsa_circ_9428,RMVar_hsa_circ_254700,RMVar_hsa_circ_63815,RMVar_hsa_circ_6314,RMVar_hsa_circ_254703,RMVar_hsa_circ_120136,RMVar_hsa_circ_108356,RMVar_hsa_circ_355294,RMVar_hsa_circ_254707,RMVar_hsa_circ_334369,RMVar_hsa_circ_103169,RMVar_hsa_circ_62254,RMVar_hsa_circ_43746,RMVar_hsa_circ_254709,RMVar_hsa_circ_355189,RMVar_hsa_circ_372200,RMVar_hsa_circ_324678,RMVar_hsa_circ_322054,RMVar_hsa_circ_100311,RMVar_hsa_circ_55128,RMVar_hsa_circ_254710,RMVar_hsa_circ_254711,RMVar_hsa_circ_254720,RMVar_hsa_circ_79843,RMVar_hsa_circ_293517,RMVar_hsa_circ_50439,RMVar_hsa_circ_34510,RMVar_hsa_circ_16409,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_54342,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_254745,RMVar_hsa_circ_349832,RMVar_hsa_circ_254744,RMVar_hsa_circ_347878,RMVar_hsa_circ_332346,RMVar_hsa_circ_294257,RMVar_hsa_circ_288942,RMVar_hsa_circ_19264,RMVar_hsa_circ_254757,RMVar_hsa_circ_87603,RMVar_hsa_circ_312922,RMVar_hsa_circ_254755,RMVar_hsa_circ_254756,RMVar_hsa_circ_50049,RMVar_hsa_circ_349698,RMVar_hsa_circ_313275,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_254763,RMVar_hsa_circ_254764,RMVar_hsa_circ_254762,RMVar_hsa_circ_254759,RMVar_hsa_circ_254760,RMVar_hsa_circ_254758,RMVar_hsa_circ_254775,RMVar_hsa_circ_298297,RMVar_hsa_circ_254769,RMVar_hsa_circ_330673,RMVar_hsa_circ_332870,RMVar_hsa_circ_322670,RMVar_hsa_circ_48253,RMVar_hsa_circ_49484,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_292962,RMVar_hsa_circ_275014,RMVar_hsa_circ_254777,RMVar_hsa_circ_254776,RMVar_hsa_circ_28404,RMVar_hsa_circ_5209,RMVar_hsa_circ_254773,RMVar_hsa_circ_254774,RMVar_hsa_circ_280042,RMVar_hsa_circ_348271,RMVar_hsa_circ_344085,RMVar_hsa_circ_282877,RMVar_hsa_circ_254781,RMVar_hsa_circ_298072,RMVar_hsa_circ_319301,RMVar_hsa_circ_293225,RMVar_hsa_circ_283910,RMVar_hsa_circ_273049,RMVar_hsa_circ_280533,RMVar_hsa_circ_53314,RMVar_hsa_circ_254784,RMVar_hsa_circ_254786,RMVar_hsa_circ_254788,RMVar_hsa_circ_21231,RMVar_hsa_circ_254787,RMVar_hsa_circ_254785,RMVar_hsa_circ_254783,RMVar_hsa_circ_93272,RMVar_hsa_circ_254789 10319 RMVar_ID_10319 Human_SNP_ID_385203553 A-to-I Human chr8 - 140820118 140820101 140820119 TCCAGTCTGGGCGACAGAGTGAGACCCTATTTAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA TCCAGTCTGGGCGACAGAGTGAGACCCTATT__________________AAAAAAAAAAAAAAAA TTTTTTTTTTTTTTTTTTA T PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1356383791 Functional Loss DEL dbSNP153 32..49 33 - - - RMVar_hsa_circ_101087,RMVar_hsa_circ_254695,RMVar_hsa_circ_119341,RMVar_hsa_circ_9428,RMVar_hsa_circ_254700,RMVar_hsa_circ_63815,RMVar_hsa_circ_6314,RMVar_hsa_circ_254703,RMVar_hsa_circ_120136,RMVar_hsa_circ_108356,RMVar_hsa_circ_355294,RMVar_hsa_circ_254707,RMVar_hsa_circ_334369,RMVar_hsa_circ_103169,RMVar_hsa_circ_62254,RMVar_hsa_circ_43746,RMVar_hsa_circ_254709,RMVar_hsa_circ_355189,RMVar_hsa_circ_372200,RMVar_hsa_circ_324678,RMVar_hsa_circ_322054,RMVar_hsa_circ_100311,RMVar_hsa_circ_55128,RMVar_hsa_circ_254710,RMVar_hsa_circ_254711,RMVar_hsa_circ_254720,RMVar_hsa_circ_79843,RMVar_hsa_circ_293517,RMVar_hsa_circ_50439,RMVar_hsa_circ_34510,RMVar_hsa_circ_16409,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_54342,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_254745,RMVar_hsa_circ_349832,RMVar_hsa_circ_254744,RMVar_hsa_circ_347878,RMVar_hsa_circ_332346,RMVar_hsa_circ_294257,RMVar_hsa_circ_288942,RMVar_hsa_circ_19264,RMVar_hsa_circ_254757,RMVar_hsa_circ_87603,RMVar_hsa_circ_312922,RMVar_hsa_circ_254755,RMVar_hsa_circ_254756,RMVar_hsa_circ_50049,RMVar_hsa_circ_349698,RMVar_hsa_circ_313275,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_254763,RMVar_hsa_circ_254764,RMVar_hsa_circ_254762,RMVar_hsa_circ_254759,RMVar_hsa_circ_254760,RMVar_hsa_circ_254758,RMVar_hsa_circ_254775,RMVar_hsa_circ_298297,RMVar_hsa_circ_254769,RMVar_hsa_circ_330673,RMVar_hsa_circ_332870,RMVar_hsa_circ_322670,RMVar_hsa_circ_48253,RMVar_hsa_circ_49484,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_292962,RMVar_hsa_circ_275014,RMVar_hsa_circ_254777,RMVar_hsa_circ_254776,RMVar_hsa_circ_28404,RMVar_hsa_circ_5209,RMVar_hsa_circ_254773,RMVar_hsa_circ_254774,RMVar_hsa_circ_280042,RMVar_hsa_circ_348271,RMVar_hsa_circ_344085,RMVar_hsa_circ_282877,RMVar_hsa_circ_254781,RMVar_hsa_circ_298072,RMVar_hsa_circ_319301,RMVar_hsa_circ_293225,RMVar_hsa_circ_283910,RMVar_hsa_circ_273049,RMVar_hsa_circ_280533,RMVar_hsa_circ_53314,RMVar_hsa_circ_254784,RMVar_hsa_circ_254786,RMVar_hsa_circ_254788,RMVar_hsa_circ_21231,RMVar_hsa_circ_254787,RMVar_hsa_circ_254785,RMVar_hsa_circ_254783,RMVar_hsa_circ_93272,RMVar_hsa_circ_254789 10320 RMVar_ID_10320 Human_SNP_ID_385203556 A-to-I Human chr8 - 140820118 140820102 140820119 TCCAGTCTGGGCGACAGAGTGAGACCCTATTTAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA TCCAGTCTGGGCGACAGAGTGAGACCCTATT_________________AAAAAAAAAAAAAAAAA TTTTTTTTTTTTTTTTTA T PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1423474189 Functional Loss DEL dbSNP153 32..48 33 - - - RMVar_hsa_circ_101087,RMVar_hsa_circ_254695,RMVar_hsa_circ_119341,RMVar_hsa_circ_9428,RMVar_hsa_circ_254700,RMVar_hsa_circ_63815,RMVar_hsa_circ_6314,RMVar_hsa_circ_254703,RMVar_hsa_circ_120136,RMVar_hsa_circ_108356,RMVar_hsa_circ_355294,RMVar_hsa_circ_254707,RMVar_hsa_circ_334369,RMVar_hsa_circ_103169,RMVar_hsa_circ_62254,RMVar_hsa_circ_43746,RMVar_hsa_circ_254709,RMVar_hsa_circ_355189,RMVar_hsa_circ_372200,RMVar_hsa_circ_324678,RMVar_hsa_circ_322054,RMVar_hsa_circ_100311,RMVar_hsa_circ_55128,RMVar_hsa_circ_254710,RMVar_hsa_circ_254711,RMVar_hsa_circ_254720,RMVar_hsa_circ_79843,RMVar_hsa_circ_293517,RMVar_hsa_circ_50439,RMVar_hsa_circ_34510,RMVar_hsa_circ_16409,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_54342,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_254745,RMVar_hsa_circ_349832,RMVar_hsa_circ_254744,RMVar_hsa_circ_347878,RMVar_hsa_circ_332346,RMVar_hsa_circ_294257,RMVar_hsa_circ_288942,RMVar_hsa_circ_19264,RMVar_hsa_circ_254757,RMVar_hsa_circ_87603,RMVar_hsa_circ_312922,RMVar_hsa_circ_254755,RMVar_hsa_circ_254756,RMVar_hsa_circ_50049,RMVar_hsa_circ_349698,RMVar_hsa_circ_313275,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_254763,RMVar_hsa_circ_254764,RMVar_hsa_circ_254762,RMVar_hsa_circ_254759,RMVar_hsa_circ_254760,RMVar_hsa_circ_254758,RMVar_hsa_circ_254775,RMVar_hsa_circ_298297,RMVar_hsa_circ_254769,RMVar_hsa_circ_330673,RMVar_hsa_circ_332870,RMVar_hsa_circ_322670,RMVar_hsa_circ_48253,RMVar_hsa_circ_49484,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_292962,RMVar_hsa_circ_275014,RMVar_hsa_circ_254777,RMVar_hsa_circ_254776,RMVar_hsa_circ_28404,RMVar_hsa_circ_5209,RMVar_hsa_circ_254773,RMVar_hsa_circ_254774,RMVar_hsa_circ_280042,RMVar_hsa_circ_348271,RMVar_hsa_circ_344085,RMVar_hsa_circ_282877,RMVar_hsa_circ_254781,RMVar_hsa_circ_298072,RMVar_hsa_circ_319301,RMVar_hsa_circ_293225,RMVar_hsa_circ_283910,RMVar_hsa_circ_273049,RMVar_hsa_circ_280533,RMVar_hsa_circ_53314,RMVar_hsa_circ_254784,RMVar_hsa_circ_254786,RMVar_hsa_circ_254788,RMVar_hsa_circ_21231,RMVar_hsa_circ_254787,RMVar_hsa_circ_254785,RMVar_hsa_circ_254783,RMVar_hsa_circ_93272,RMVar_hsa_circ_254789 10321 RMVar_ID_10321 Human_SNP_ID_385203557 A-to-I Human chr8 - 140820118 140820103 140820119 TCCAGTCTGGGCGACAGAGTGAGACCCTATTTAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA TCCAGTCTGGGCGACAGAGTGAGACCCTATT________________AAAAAAAAAAAAAAAAAA TTTTTTTTTTTTTTTTA T PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277760306 Functional Loss DEL dbSNP153 32..47 33 - - - RMVar_hsa_circ_101087,RMVar_hsa_circ_254695,RMVar_hsa_circ_119341,RMVar_hsa_circ_9428,RMVar_hsa_circ_254700,RMVar_hsa_circ_63815,RMVar_hsa_circ_6314,RMVar_hsa_circ_254703,RMVar_hsa_circ_120136,RMVar_hsa_circ_108356,RMVar_hsa_circ_355294,RMVar_hsa_circ_254707,RMVar_hsa_circ_334369,RMVar_hsa_circ_103169,RMVar_hsa_circ_62254,RMVar_hsa_circ_43746,RMVar_hsa_circ_254709,RMVar_hsa_circ_355189,RMVar_hsa_circ_372200,RMVar_hsa_circ_324678,RMVar_hsa_circ_322054,RMVar_hsa_circ_100311,RMVar_hsa_circ_55128,RMVar_hsa_circ_254710,RMVar_hsa_circ_254711,RMVar_hsa_circ_254720,RMVar_hsa_circ_79843,RMVar_hsa_circ_293517,RMVar_hsa_circ_50439,RMVar_hsa_circ_34510,RMVar_hsa_circ_16409,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_54342,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_254745,RMVar_hsa_circ_349832,RMVar_hsa_circ_254744,RMVar_hsa_circ_347878,RMVar_hsa_circ_332346,RMVar_hsa_circ_294257,RMVar_hsa_circ_288942,RMVar_hsa_circ_19264,RMVar_hsa_circ_254757,RMVar_hsa_circ_87603,RMVar_hsa_circ_312922,RMVar_hsa_circ_254755,RMVar_hsa_circ_254756,RMVar_hsa_circ_50049,RMVar_hsa_circ_349698,RMVar_hsa_circ_313275,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_254763,RMVar_hsa_circ_254764,RMVar_hsa_circ_254762,RMVar_hsa_circ_254759,RMVar_hsa_circ_254760,RMVar_hsa_circ_254758,RMVar_hsa_circ_254775,RMVar_hsa_circ_298297,RMVar_hsa_circ_254769,RMVar_hsa_circ_330673,RMVar_hsa_circ_332870,RMVar_hsa_circ_322670,RMVar_hsa_circ_48253,RMVar_hsa_circ_49484,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_292962,RMVar_hsa_circ_275014,RMVar_hsa_circ_254777,RMVar_hsa_circ_254776,RMVar_hsa_circ_28404,RMVar_hsa_circ_5209,RMVar_hsa_circ_254773,RMVar_hsa_circ_254774,RMVar_hsa_circ_280042,RMVar_hsa_circ_348271,RMVar_hsa_circ_344085,RMVar_hsa_circ_282877,RMVar_hsa_circ_254781,RMVar_hsa_circ_298072,RMVar_hsa_circ_319301,RMVar_hsa_circ_293225,RMVar_hsa_circ_283910,RMVar_hsa_circ_273049,RMVar_hsa_circ_280533,RMVar_hsa_circ_53314,RMVar_hsa_circ_254784,RMVar_hsa_circ_254786,RMVar_hsa_circ_254788,RMVar_hsa_circ_21231,RMVar_hsa_circ_254787,RMVar_hsa_circ_254785,RMVar_hsa_circ_254783,RMVar_hsa_circ_93272,RMVar_hsa_circ_254789 10322 RMVar_ID_10322 Human_SNP_ID_385203559 A-to-I Human chr8 - 140820118 140820104 140820119 TCCAGTCTGGGCGACAGAGTGAGACCCTATTTAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA TCCAGTCTGGGCGACAGAGTGAGACCCTATT_______________AAAAAAAAAAAAAAAAAAA TTTTTTTTTTTTTTTA T PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1471845947 Functional Loss DEL dbSNP153 32..46 33 - - - RMVar_hsa_circ_101087,RMVar_hsa_circ_254695,RMVar_hsa_circ_119341,RMVar_hsa_circ_9428,RMVar_hsa_circ_254700,RMVar_hsa_circ_63815,RMVar_hsa_circ_6314,RMVar_hsa_circ_254703,RMVar_hsa_circ_120136,RMVar_hsa_circ_108356,RMVar_hsa_circ_355294,RMVar_hsa_circ_254707,RMVar_hsa_circ_334369,RMVar_hsa_circ_103169,RMVar_hsa_circ_62254,RMVar_hsa_circ_43746,RMVar_hsa_circ_254709,RMVar_hsa_circ_355189,RMVar_hsa_circ_372200,RMVar_hsa_circ_324678,RMVar_hsa_circ_322054,RMVar_hsa_circ_100311,RMVar_hsa_circ_55128,RMVar_hsa_circ_254710,RMVar_hsa_circ_254711,RMVar_hsa_circ_254720,RMVar_hsa_circ_79843,RMVar_hsa_circ_293517,RMVar_hsa_circ_50439,RMVar_hsa_circ_34510,RMVar_hsa_circ_16409,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_54342,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_254745,RMVar_hsa_circ_349832,RMVar_hsa_circ_254744,RMVar_hsa_circ_347878,RMVar_hsa_circ_332346,RMVar_hsa_circ_294257,RMVar_hsa_circ_288942,RMVar_hsa_circ_19264,RMVar_hsa_circ_254757,RMVar_hsa_circ_87603,RMVar_hsa_circ_312922,RMVar_hsa_circ_254755,RMVar_hsa_circ_254756,RMVar_hsa_circ_50049,RMVar_hsa_circ_349698,RMVar_hsa_circ_313275,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_254763,RMVar_hsa_circ_254764,RMVar_hsa_circ_254762,RMVar_hsa_circ_254759,RMVar_hsa_circ_254760,RMVar_hsa_circ_254758,RMVar_hsa_circ_254775,RMVar_hsa_circ_298297,RMVar_hsa_circ_254769,RMVar_hsa_circ_330673,RMVar_hsa_circ_332870,RMVar_hsa_circ_322670,RMVar_hsa_circ_48253,RMVar_hsa_circ_49484,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_292962,RMVar_hsa_circ_275014,RMVar_hsa_circ_254777,RMVar_hsa_circ_254776,RMVar_hsa_circ_28404,RMVar_hsa_circ_5209,RMVar_hsa_circ_254773,RMVar_hsa_circ_254774,RMVar_hsa_circ_280042,RMVar_hsa_circ_348271,RMVar_hsa_circ_344085,RMVar_hsa_circ_282877,RMVar_hsa_circ_254781,RMVar_hsa_circ_298072,RMVar_hsa_circ_319301,RMVar_hsa_circ_293225,RMVar_hsa_circ_283910,RMVar_hsa_circ_273049,RMVar_hsa_circ_280533,RMVar_hsa_circ_53314,RMVar_hsa_circ_254784,RMVar_hsa_circ_254786,RMVar_hsa_circ_254788,RMVar_hsa_circ_21231,RMVar_hsa_circ_254787,RMVar_hsa_circ_254785,RMVar_hsa_circ_254783,RMVar_hsa_circ_93272,RMVar_hsa_circ_254789 10323 RMVar_ID_10323 Human_SNP_ID_385203560 A-to-I Human chr8 - 140820118 140820105 140820119 TCCAGTCTGGGCGACAGAGTGAGACCCTATTTAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA TCCAGTCTGGGCGACAGAGTGAGACCCTATT______________AAAAAAAAAAAAAAAAAAAA TTTTTTTTTTTTTTA T PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1349839595 Functional Loss DEL dbSNP153 32..45 33 - - - RMVar_hsa_circ_101087,RMVar_hsa_circ_254695,RMVar_hsa_circ_119341,RMVar_hsa_circ_9428,RMVar_hsa_circ_254700,RMVar_hsa_circ_63815,RMVar_hsa_circ_6314,RMVar_hsa_circ_254703,RMVar_hsa_circ_120136,RMVar_hsa_circ_108356,RMVar_hsa_circ_355294,RMVar_hsa_circ_254707,RMVar_hsa_circ_334369,RMVar_hsa_circ_103169,RMVar_hsa_circ_62254,RMVar_hsa_circ_43746,RMVar_hsa_circ_254709,RMVar_hsa_circ_355189,RMVar_hsa_circ_372200,RMVar_hsa_circ_324678,RMVar_hsa_circ_322054,RMVar_hsa_circ_100311,RMVar_hsa_circ_55128,RMVar_hsa_circ_254710,RMVar_hsa_circ_254711,RMVar_hsa_circ_254720,RMVar_hsa_circ_79843,RMVar_hsa_circ_293517,RMVar_hsa_circ_50439,RMVar_hsa_circ_34510,RMVar_hsa_circ_16409,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_54342,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_254745,RMVar_hsa_circ_349832,RMVar_hsa_circ_254744,RMVar_hsa_circ_347878,RMVar_hsa_circ_332346,RMVar_hsa_circ_294257,RMVar_hsa_circ_288942,RMVar_hsa_circ_19264,RMVar_hsa_circ_254757,RMVar_hsa_circ_87603,RMVar_hsa_circ_312922,RMVar_hsa_circ_254755,RMVar_hsa_circ_254756,RMVar_hsa_circ_50049,RMVar_hsa_circ_349698,RMVar_hsa_circ_313275,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_254763,RMVar_hsa_circ_254764,RMVar_hsa_circ_254762,RMVar_hsa_circ_254759,RMVar_hsa_circ_254760,RMVar_hsa_circ_254758,RMVar_hsa_circ_254775,RMVar_hsa_circ_298297,RMVar_hsa_circ_254769,RMVar_hsa_circ_330673,RMVar_hsa_circ_332870,RMVar_hsa_circ_322670,RMVar_hsa_circ_48253,RMVar_hsa_circ_49484,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_292962,RMVar_hsa_circ_275014,RMVar_hsa_circ_254777,RMVar_hsa_circ_254776,RMVar_hsa_circ_28404,RMVar_hsa_circ_5209,RMVar_hsa_circ_254773,RMVar_hsa_circ_254774,RMVar_hsa_circ_280042,RMVar_hsa_circ_348271,RMVar_hsa_circ_344085,RMVar_hsa_circ_282877,RMVar_hsa_circ_254781,RMVar_hsa_circ_298072,RMVar_hsa_circ_319301,RMVar_hsa_circ_293225,RMVar_hsa_circ_283910,RMVar_hsa_circ_273049,RMVar_hsa_circ_280533,RMVar_hsa_circ_53314,RMVar_hsa_circ_254784,RMVar_hsa_circ_254786,RMVar_hsa_circ_254788,RMVar_hsa_circ_21231,RMVar_hsa_circ_254787,RMVar_hsa_circ_254785,RMVar_hsa_circ_254783,RMVar_hsa_circ_93272,RMVar_hsa_circ_254789 10324 RMVar_ID_10324 Human_SNP_ID_385203562 A-to-I Human chr8 - 140820118 140820106 140820119 TCCAGTCTGGGCGACAGAGTGAGACCCTATTTAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA TCCAGTCTGGGCGACAGAGTGAGACCCTATT_____________AAAAAAAAAAAAAAAAAAAAA TTTTTTTTTTTTTA T PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1240654731 Functional Loss DEL dbSNP153 32..44 33 - - - RMVar_hsa_circ_101087,RMVar_hsa_circ_254695,RMVar_hsa_circ_119341,RMVar_hsa_circ_9428,RMVar_hsa_circ_254700,RMVar_hsa_circ_63815,RMVar_hsa_circ_6314,RMVar_hsa_circ_254703,RMVar_hsa_circ_120136,RMVar_hsa_circ_108356,RMVar_hsa_circ_355294,RMVar_hsa_circ_254707,RMVar_hsa_circ_334369,RMVar_hsa_circ_103169,RMVar_hsa_circ_62254,RMVar_hsa_circ_43746,RMVar_hsa_circ_254709,RMVar_hsa_circ_355189,RMVar_hsa_circ_372200,RMVar_hsa_circ_324678,RMVar_hsa_circ_322054,RMVar_hsa_circ_100311,RMVar_hsa_circ_55128,RMVar_hsa_circ_254710,RMVar_hsa_circ_254711,RMVar_hsa_circ_254720,RMVar_hsa_circ_79843,RMVar_hsa_circ_293517,RMVar_hsa_circ_50439,RMVar_hsa_circ_34510,RMVar_hsa_circ_16409,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_54342,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_254745,RMVar_hsa_circ_349832,RMVar_hsa_circ_254744,RMVar_hsa_circ_347878,RMVar_hsa_circ_332346,RMVar_hsa_circ_294257,RMVar_hsa_circ_288942,RMVar_hsa_circ_19264,RMVar_hsa_circ_254757,RMVar_hsa_circ_87603,RMVar_hsa_circ_312922,RMVar_hsa_circ_254755,RMVar_hsa_circ_254756,RMVar_hsa_circ_50049,RMVar_hsa_circ_349698,RMVar_hsa_circ_313275,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_254763,RMVar_hsa_circ_254764,RMVar_hsa_circ_254762,RMVar_hsa_circ_254759,RMVar_hsa_circ_254760,RMVar_hsa_circ_254758,RMVar_hsa_circ_254775,RMVar_hsa_circ_298297,RMVar_hsa_circ_254769,RMVar_hsa_circ_330673,RMVar_hsa_circ_332870,RMVar_hsa_circ_322670,RMVar_hsa_circ_48253,RMVar_hsa_circ_49484,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_292962,RMVar_hsa_circ_275014,RMVar_hsa_circ_254777,RMVar_hsa_circ_254776,RMVar_hsa_circ_28404,RMVar_hsa_circ_5209,RMVar_hsa_circ_254773,RMVar_hsa_circ_254774,RMVar_hsa_circ_280042,RMVar_hsa_circ_348271,RMVar_hsa_circ_344085,RMVar_hsa_circ_282877,RMVar_hsa_circ_254781,RMVar_hsa_circ_298072,RMVar_hsa_circ_319301,RMVar_hsa_circ_293225,RMVar_hsa_circ_283910,RMVar_hsa_circ_273049,RMVar_hsa_circ_280533,RMVar_hsa_circ_53314,RMVar_hsa_circ_254784,RMVar_hsa_circ_254786,RMVar_hsa_circ_254788,RMVar_hsa_circ_21231,RMVar_hsa_circ_254787,RMVar_hsa_circ_254785,RMVar_hsa_circ_254783,RMVar_hsa_circ_93272,RMVar_hsa_circ_254789 10325 RMVar_ID_10325 Human_SNP_ID_385203563 A-to-I Human chr8 - 140820118 140820107 140820119 TCCAGTCTGGGCGACAGAGTGAGACCCTATTTAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA TCCAGTCTGGGCGACAGAGTGAGACCCTATT____________AAAAAAAAAAAAAAAAAAAAAA TTTTTTTTTTTTA T PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1287845709 Functional Loss DEL dbSNP153 32..43 33 - - - RMVar_hsa_circ_101087,RMVar_hsa_circ_254695,RMVar_hsa_circ_119341,RMVar_hsa_circ_9428,RMVar_hsa_circ_254700,RMVar_hsa_circ_63815,RMVar_hsa_circ_6314,RMVar_hsa_circ_254703,RMVar_hsa_circ_120136,RMVar_hsa_circ_108356,RMVar_hsa_circ_355294,RMVar_hsa_circ_254707,RMVar_hsa_circ_334369,RMVar_hsa_circ_103169,RMVar_hsa_circ_62254,RMVar_hsa_circ_43746,RMVar_hsa_circ_254709,RMVar_hsa_circ_355189,RMVar_hsa_circ_372200,RMVar_hsa_circ_324678,RMVar_hsa_circ_322054,RMVar_hsa_circ_100311,RMVar_hsa_circ_55128,RMVar_hsa_circ_254710,RMVar_hsa_circ_254711,RMVar_hsa_circ_254720,RMVar_hsa_circ_79843,RMVar_hsa_circ_293517,RMVar_hsa_circ_50439,RMVar_hsa_circ_34510,RMVar_hsa_circ_16409,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_54342,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_254745,RMVar_hsa_circ_349832,RMVar_hsa_circ_254744,RMVar_hsa_circ_347878,RMVar_hsa_circ_332346,RMVar_hsa_circ_294257,RMVar_hsa_circ_288942,RMVar_hsa_circ_19264,RMVar_hsa_circ_254757,RMVar_hsa_circ_87603,RMVar_hsa_circ_312922,RMVar_hsa_circ_254755,RMVar_hsa_circ_254756,RMVar_hsa_circ_50049,RMVar_hsa_circ_349698,RMVar_hsa_circ_313275,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_254763,RMVar_hsa_circ_254764,RMVar_hsa_circ_254762,RMVar_hsa_circ_254759,RMVar_hsa_circ_254760,RMVar_hsa_circ_254758,RMVar_hsa_circ_254775,RMVar_hsa_circ_298297,RMVar_hsa_circ_254769,RMVar_hsa_circ_330673,RMVar_hsa_circ_332870,RMVar_hsa_circ_322670,RMVar_hsa_circ_48253,RMVar_hsa_circ_49484,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_292962,RMVar_hsa_circ_275014,RMVar_hsa_circ_254777,RMVar_hsa_circ_254776,RMVar_hsa_circ_28404,RMVar_hsa_circ_5209,RMVar_hsa_circ_254773,RMVar_hsa_circ_254774,RMVar_hsa_circ_280042,RMVar_hsa_circ_348271,RMVar_hsa_circ_344085,RMVar_hsa_circ_282877,RMVar_hsa_circ_254781,RMVar_hsa_circ_298072,RMVar_hsa_circ_319301,RMVar_hsa_circ_293225,RMVar_hsa_circ_283910,RMVar_hsa_circ_273049,RMVar_hsa_circ_280533,RMVar_hsa_circ_53314,RMVar_hsa_circ_254784,RMVar_hsa_circ_254786,RMVar_hsa_circ_254788,RMVar_hsa_circ_21231,RMVar_hsa_circ_254787,RMVar_hsa_circ_254785,RMVar_hsa_circ_254783,RMVar_hsa_circ_93272,RMVar_hsa_circ_254789 10326 RMVar_ID_10326 Human_SNP_ID_385203565 A-to-I Human chr8 - 140820118 140820108 140820119 TCCAGTCTGGGCGACAGAGTGAGACCCTATTTAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA TCCAGTCTGGGCGACAGAGTGAGACCCTATT___________AAAAAAAAAAAAAAAAAAAAAAA TTTTTTTTTTTA T PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1489735485 Functional Loss DEL dbSNP153 32..42 33 - - - RMVar_hsa_circ_101087,RMVar_hsa_circ_254695,RMVar_hsa_circ_119341,RMVar_hsa_circ_9428,RMVar_hsa_circ_254700,RMVar_hsa_circ_63815,RMVar_hsa_circ_6314,RMVar_hsa_circ_254703,RMVar_hsa_circ_120136,RMVar_hsa_circ_108356,RMVar_hsa_circ_355294,RMVar_hsa_circ_254707,RMVar_hsa_circ_334369,RMVar_hsa_circ_103169,RMVar_hsa_circ_62254,RMVar_hsa_circ_43746,RMVar_hsa_circ_254709,RMVar_hsa_circ_355189,RMVar_hsa_circ_372200,RMVar_hsa_circ_324678,RMVar_hsa_circ_322054,RMVar_hsa_circ_100311,RMVar_hsa_circ_55128,RMVar_hsa_circ_254710,RMVar_hsa_circ_254711,RMVar_hsa_circ_254720,RMVar_hsa_circ_79843,RMVar_hsa_circ_293517,RMVar_hsa_circ_50439,RMVar_hsa_circ_34510,RMVar_hsa_circ_16409,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_54342,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_254745,RMVar_hsa_circ_349832,RMVar_hsa_circ_254744,RMVar_hsa_circ_347878,RMVar_hsa_circ_332346,RMVar_hsa_circ_294257,RMVar_hsa_circ_288942,RMVar_hsa_circ_19264,RMVar_hsa_circ_254757,RMVar_hsa_circ_87603,RMVar_hsa_circ_312922,RMVar_hsa_circ_254755,RMVar_hsa_circ_254756,RMVar_hsa_circ_50049,RMVar_hsa_circ_349698,RMVar_hsa_circ_313275,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_254763,RMVar_hsa_circ_254764,RMVar_hsa_circ_254762,RMVar_hsa_circ_254759,RMVar_hsa_circ_254760,RMVar_hsa_circ_254758,RMVar_hsa_circ_254775,RMVar_hsa_circ_298297,RMVar_hsa_circ_254769,RMVar_hsa_circ_330673,RMVar_hsa_circ_332870,RMVar_hsa_circ_322670,RMVar_hsa_circ_48253,RMVar_hsa_circ_49484,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_292962,RMVar_hsa_circ_275014,RMVar_hsa_circ_254777,RMVar_hsa_circ_254776,RMVar_hsa_circ_28404,RMVar_hsa_circ_5209,RMVar_hsa_circ_254773,RMVar_hsa_circ_254774,RMVar_hsa_circ_280042,RMVar_hsa_circ_348271,RMVar_hsa_circ_344085,RMVar_hsa_circ_282877,RMVar_hsa_circ_254781,RMVar_hsa_circ_298072,RMVar_hsa_circ_319301,RMVar_hsa_circ_293225,RMVar_hsa_circ_283910,RMVar_hsa_circ_273049,RMVar_hsa_circ_280533,RMVar_hsa_circ_53314,RMVar_hsa_circ_254784,RMVar_hsa_circ_254786,RMVar_hsa_circ_254788,RMVar_hsa_circ_21231,RMVar_hsa_circ_254787,RMVar_hsa_circ_254785,RMVar_hsa_circ_254783,RMVar_hsa_circ_93272,RMVar_hsa_circ_254789 10327 RMVar_ID_10327 Human_SNP_ID_385203567 A-to-I Human chr8 - 140820118 140820109 140820119 TCCAGTCTGGGCGACAGAGTGAGACCCTATTTAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA TCCAGTCTGGGCGACAGAGTGAGACCCTATT__________AAAAAAAAAAAAAAAAAAAAAAAA TTTTTTTTTTA T PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1221208896 Functional Loss DEL dbSNP153 32..41 33 - - - RMVar_hsa_circ_101087,RMVar_hsa_circ_254695,RMVar_hsa_circ_119341,RMVar_hsa_circ_9428,RMVar_hsa_circ_254700,RMVar_hsa_circ_63815,RMVar_hsa_circ_6314,RMVar_hsa_circ_254703,RMVar_hsa_circ_120136,RMVar_hsa_circ_108356,RMVar_hsa_circ_355294,RMVar_hsa_circ_254707,RMVar_hsa_circ_334369,RMVar_hsa_circ_103169,RMVar_hsa_circ_62254,RMVar_hsa_circ_43746,RMVar_hsa_circ_254709,RMVar_hsa_circ_355189,RMVar_hsa_circ_372200,RMVar_hsa_circ_324678,RMVar_hsa_circ_322054,RMVar_hsa_circ_100311,RMVar_hsa_circ_55128,RMVar_hsa_circ_254710,RMVar_hsa_circ_254711,RMVar_hsa_circ_254720,RMVar_hsa_circ_79843,RMVar_hsa_circ_293517,RMVar_hsa_circ_50439,RMVar_hsa_circ_34510,RMVar_hsa_circ_16409,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_54342,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_254745,RMVar_hsa_circ_349832,RMVar_hsa_circ_254744,RMVar_hsa_circ_347878,RMVar_hsa_circ_332346,RMVar_hsa_circ_294257,RMVar_hsa_circ_288942,RMVar_hsa_circ_19264,RMVar_hsa_circ_254757,RMVar_hsa_circ_87603,RMVar_hsa_circ_312922,RMVar_hsa_circ_254755,RMVar_hsa_circ_254756,RMVar_hsa_circ_50049,RMVar_hsa_circ_349698,RMVar_hsa_circ_313275,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_254763,RMVar_hsa_circ_254764,RMVar_hsa_circ_254762,RMVar_hsa_circ_254759,RMVar_hsa_circ_254760,RMVar_hsa_circ_254758,RMVar_hsa_circ_254775,RMVar_hsa_circ_298297,RMVar_hsa_circ_254769,RMVar_hsa_circ_330673,RMVar_hsa_circ_332870,RMVar_hsa_circ_322670,RMVar_hsa_circ_48253,RMVar_hsa_circ_49484,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_292962,RMVar_hsa_circ_275014,RMVar_hsa_circ_254777,RMVar_hsa_circ_254776,RMVar_hsa_circ_28404,RMVar_hsa_circ_5209,RMVar_hsa_circ_254773,RMVar_hsa_circ_254774,RMVar_hsa_circ_280042,RMVar_hsa_circ_348271,RMVar_hsa_circ_344085,RMVar_hsa_circ_282877,RMVar_hsa_circ_254781,RMVar_hsa_circ_298072,RMVar_hsa_circ_319301,RMVar_hsa_circ_293225,RMVar_hsa_circ_283910,RMVar_hsa_circ_273049,RMVar_hsa_circ_280533,RMVar_hsa_circ_53314,RMVar_hsa_circ_254784,RMVar_hsa_circ_254786,RMVar_hsa_circ_254788,RMVar_hsa_circ_21231,RMVar_hsa_circ_254787,RMVar_hsa_circ_254785,RMVar_hsa_circ_254783,RMVar_hsa_circ_93272,RMVar_hsa_circ_254789 10328 RMVar_ID_10328 Human_SNP_ID_385203568 A-to-I Human chr8 - 140820118 140820110 140820119 TCCAGTCTGGGCGACAGAGTGAGACCCTATTTAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA TCCAGTCTGGGCGACAGAGTGAGACCCTATT_________AAAAAAAAAAAAAAAAAAAAAAAAA TTTTTTTTTA T PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1267445779 Functional Loss DEL dbSNP153 32..40 33 - - - RMVar_hsa_circ_101087,RMVar_hsa_circ_254695,RMVar_hsa_circ_119341,RMVar_hsa_circ_9428,RMVar_hsa_circ_254700,RMVar_hsa_circ_63815,RMVar_hsa_circ_6314,RMVar_hsa_circ_254703,RMVar_hsa_circ_120136,RMVar_hsa_circ_108356,RMVar_hsa_circ_355294,RMVar_hsa_circ_254707,RMVar_hsa_circ_334369,RMVar_hsa_circ_103169,RMVar_hsa_circ_62254,RMVar_hsa_circ_43746,RMVar_hsa_circ_254709,RMVar_hsa_circ_355189,RMVar_hsa_circ_372200,RMVar_hsa_circ_324678,RMVar_hsa_circ_322054,RMVar_hsa_circ_100311,RMVar_hsa_circ_55128,RMVar_hsa_circ_254710,RMVar_hsa_circ_254711,RMVar_hsa_circ_254720,RMVar_hsa_circ_79843,RMVar_hsa_circ_293517,RMVar_hsa_circ_50439,RMVar_hsa_circ_34510,RMVar_hsa_circ_16409,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_54342,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_254745,RMVar_hsa_circ_349832,RMVar_hsa_circ_254744,RMVar_hsa_circ_347878,RMVar_hsa_circ_332346,RMVar_hsa_circ_294257,RMVar_hsa_circ_288942,RMVar_hsa_circ_19264,RMVar_hsa_circ_254757,RMVar_hsa_circ_87603,RMVar_hsa_circ_312922,RMVar_hsa_circ_254755,RMVar_hsa_circ_254756,RMVar_hsa_circ_50049,RMVar_hsa_circ_349698,RMVar_hsa_circ_313275,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_254763,RMVar_hsa_circ_254764,RMVar_hsa_circ_254762,RMVar_hsa_circ_254759,RMVar_hsa_circ_254760,RMVar_hsa_circ_254758,RMVar_hsa_circ_254775,RMVar_hsa_circ_298297,RMVar_hsa_circ_254769,RMVar_hsa_circ_330673,RMVar_hsa_circ_332870,RMVar_hsa_circ_322670,RMVar_hsa_circ_48253,RMVar_hsa_circ_49484,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_292962,RMVar_hsa_circ_275014,RMVar_hsa_circ_254777,RMVar_hsa_circ_254776,RMVar_hsa_circ_28404,RMVar_hsa_circ_5209,RMVar_hsa_circ_254773,RMVar_hsa_circ_254774,RMVar_hsa_circ_280042,RMVar_hsa_circ_348271,RMVar_hsa_circ_344085,RMVar_hsa_circ_282877,RMVar_hsa_circ_254781,RMVar_hsa_circ_298072,RMVar_hsa_circ_319301,RMVar_hsa_circ_293225,RMVar_hsa_circ_283910,RMVar_hsa_circ_273049,RMVar_hsa_circ_280533,RMVar_hsa_circ_53314,RMVar_hsa_circ_254784,RMVar_hsa_circ_254786,RMVar_hsa_circ_254788,RMVar_hsa_circ_21231,RMVar_hsa_circ_254787,RMVar_hsa_circ_254785,RMVar_hsa_circ_254783,RMVar_hsa_circ_93272,RMVar_hsa_circ_254789 10329 RMVar_ID_10329 Human_SNP_ID_385203571 A-to-I Human chr8 - 140820118 140820111 140820119 TCCAGTCTGGGCGACAGAGTGAGACCCTATTTAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA TCCAGTCTGGGCGACAGAGTGAGACCCTATT________AAAAAAAAAAAAAAAAAAAAAAAAAA TTTTTTTTA T PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1452900539 Functional Loss DEL dbSNP153 32..39 33 - - - RMVar_hsa_circ_101087,RMVar_hsa_circ_254695,RMVar_hsa_circ_119341,RMVar_hsa_circ_9428,RMVar_hsa_circ_254700,RMVar_hsa_circ_63815,RMVar_hsa_circ_6314,RMVar_hsa_circ_254703,RMVar_hsa_circ_120136,RMVar_hsa_circ_108356,RMVar_hsa_circ_355294,RMVar_hsa_circ_254707,RMVar_hsa_circ_334369,RMVar_hsa_circ_103169,RMVar_hsa_circ_62254,RMVar_hsa_circ_43746,RMVar_hsa_circ_254709,RMVar_hsa_circ_355189,RMVar_hsa_circ_372200,RMVar_hsa_circ_324678,RMVar_hsa_circ_322054,RMVar_hsa_circ_100311,RMVar_hsa_circ_55128,RMVar_hsa_circ_254710,RMVar_hsa_circ_254711,RMVar_hsa_circ_254720,RMVar_hsa_circ_79843,RMVar_hsa_circ_293517,RMVar_hsa_circ_50439,RMVar_hsa_circ_34510,RMVar_hsa_circ_16409,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_54342,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_254745,RMVar_hsa_circ_349832,RMVar_hsa_circ_254744,RMVar_hsa_circ_347878,RMVar_hsa_circ_332346,RMVar_hsa_circ_294257,RMVar_hsa_circ_288942,RMVar_hsa_circ_19264,RMVar_hsa_circ_254757,RMVar_hsa_circ_87603,RMVar_hsa_circ_312922,RMVar_hsa_circ_254755,RMVar_hsa_circ_254756,RMVar_hsa_circ_50049,RMVar_hsa_circ_349698,RMVar_hsa_circ_313275,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_254763,RMVar_hsa_circ_254764,RMVar_hsa_circ_254762,RMVar_hsa_circ_254759,RMVar_hsa_circ_254760,RMVar_hsa_circ_254758,RMVar_hsa_circ_254775,RMVar_hsa_circ_298297,RMVar_hsa_circ_254769,RMVar_hsa_circ_330673,RMVar_hsa_circ_332870,RMVar_hsa_circ_322670,RMVar_hsa_circ_48253,RMVar_hsa_circ_49484,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_292962,RMVar_hsa_circ_275014,RMVar_hsa_circ_254777,RMVar_hsa_circ_254776,RMVar_hsa_circ_28404,RMVar_hsa_circ_5209,RMVar_hsa_circ_254773,RMVar_hsa_circ_254774,RMVar_hsa_circ_280042,RMVar_hsa_circ_348271,RMVar_hsa_circ_344085,RMVar_hsa_circ_282877,RMVar_hsa_circ_254781,RMVar_hsa_circ_298072,RMVar_hsa_circ_319301,RMVar_hsa_circ_293225,RMVar_hsa_circ_283910,RMVar_hsa_circ_273049,RMVar_hsa_circ_280533,RMVar_hsa_circ_53314,RMVar_hsa_circ_254784,RMVar_hsa_circ_254786,RMVar_hsa_circ_254788,RMVar_hsa_circ_21231,RMVar_hsa_circ_254787,RMVar_hsa_circ_254785,RMVar_hsa_circ_254783,RMVar_hsa_circ_93272,RMVar_hsa_circ_254789 10330 RMVar_ID_10330 Human_SNP_ID_385203572 A-to-I Human chr8 - 140820118 140820112 140820119 TCCAGTCTGGGCGACAGAGTGAGACCCTATTTAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA TCCAGTCTGGGCGACAGAGTGAGACCCTATT_______AAAAAAAAAAAAAAAAAAAAAAAAAAA TTTTTTTA T PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1179030090 Functional Loss DEL dbSNP153 32..38 33 - - - RMVar_hsa_circ_101087,RMVar_hsa_circ_254695,RMVar_hsa_circ_119341,RMVar_hsa_circ_9428,RMVar_hsa_circ_254700,RMVar_hsa_circ_63815,RMVar_hsa_circ_6314,RMVar_hsa_circ_254703,RMVar_hsa_circ_120136,RMVar_hsa_circ_108356,RMVar_hsa_circ_355294,RMVar_hsa_circ_254707,RMVar_hsa_circ_334369,RMVar_hsa_circ_103169,RMVar_hsa_circ_62254,RMVar_hsa_circ_43746,RMVar_hsa_circ_254709,RMVar_hsa_circ_355189,RMVar_hsa_circ_372200,RMVar_hsa_circ_324678,RMVar_hsa_circ_322054,RMVar_hsa_circ_100311,RMVar_hsa_circ_55128,RMVar_hsa_circ_254710,RMVar_hsa_circ_254711,RMVar_hsa_circ_254720,RMVar_hsa_circ_79843,RMVar_hsa_circ_293517,RMVar_hsa_circ_50439,RMVar_hsa_circ_34510,RMVar_hsa_circ_16409,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_54342,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_254745,RMVar_hsa_circ_349832,RMVar_hsa_circ_254744,RMVar_hsa_circ_347878,RMVar_hsa_circ_332346,RMVar_hsa_circ_294257,RMVar_hsa_circ_288942,RMVar_hsa_circ_19264,RMVar_hsa_circ_254757,RMVar_hsa_circ_87603,RMVar_hsa_circ_312922,RMVar_hsa_circ_254755,RMVar_hsa_circ_254756,RMVar_hsa_circ_50049,RMVar_hsa_circ_349698,RMVar_hsa_circ_313275,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_254763,RMVar_hsa_circ_254764,RMVar_hsa_circ_254762,RMVar_hsa_circ_254759,RMVar_hsa_circ_254760,RMVar_hsa_circ_254758,RMVar_hsa_circ_254775,RMVar_hsa_circ_298297,RMVar_hsa_circ_254769,RMVar_hsa_circ_330673,RMVar_hsa_circ_332870,RMVar_hsa_circ_322670,RMVar_hsa_circ_48253,RMVar_hsa_circ_49484,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_292962,RMVar_hsa_circ_275014,RMVar_hsa_circ_254777,RMVar_hsa_circ_254776,RMVar_hsa_circ_28404,RMVar_hsa_circ_5209,RMVar_hsa_circ_254773,RMVar_hsa_circ_254774,RMVar_hsa_circ_280042,RMVar_hsa_circ_348271,RMVar_hsa_circ_344085,RMVar_hsa_circ_282877,RMVar_hsa_circ_254781,RMVar_hsa_circ_298072,RMVar_hsa_circ_319301,RMVar_hsa_circ_293225,RMVar_hsa_circ_283910,RMVar_hsa_circ_273049,RMVar_hsa_circ_280533,RMVar_hsa_circ_53314,RMVar_hsa_circ_254784,RMVar_hsa_circ_254786,RMVar_hsa_circ_254788,RMVar_hsa_circ_21231,RMVar_hsa_circ_254787,RMVar_hsa_circ_254785,RMVar_hsa_circ_254783,RMVar_hsa_circ_93272,RMVar_hsa_circ_254789 10331 RMVar_ID_10331 Human_SNP_ID_385203573 A-to-I Human chr8 - 140820118 140820113 140820119 TCCAGTCTGGGCGACAGAGTGAGACCCTATTTAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA TCCAGTCTGGGCGACAGAGTGAGACCCTATT______AAAAAAAAAAAAAAAAAAAAAAAAAAAA TTTTTTA T PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1306149179 Functional Loss DEL dbSNP153 32..37 33 - - - RMVar_hsa_circ_101087,RMVar_hsa_circ_254695,RMVar_hsa_circ_119341,RMVar_hsa_circ_9428,RMVar_hsa_circ_254700,RMVar_hsa_circ_63815,RMVar_hsa_circ_6314,RMVar_hsa_circ_254703,RMVar_hsa_circ_120136,RMVar_hsa_circ_108356,RMVar_hsa_circ_355294,RMVar_hsa_circ_254707,RMVar_hsa_circ_334369,RMVar_hsa_circ_103169,RMVar_hsa_circ_62254,RMVar_hsa_circ_43746,RMVar_hsa_circ_254709,RMVar_hsa_circ_355189,RMVar_hsa_circ_372200,RMVar_hsa_circ_324678,RMVar_hsa_circ_322054,RMVar_hsa_circ_100311,RMVar_hsa_circ_55128,RMVar_hsa_circ_254710,RMVar_hsa_circ_254711,RMVar_hsa_circ_254720,RMVar_hsa_circ_79843,RMVar_hsa_circ_293517,RMVar_hsa_circ_50439,RMVar_hsa_circ_34510,RMVar_hsa_circ_16409,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_54342,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_254745,RMVar_hsa_circ_349832,RMVar_hsa_circ_254744,RMVar_hsa_circ_347878,RMVar_hsa_circ_332346,RMVar_hsa_circ_294257,RMVar_hsa_circ_288942,RMVar_hsa_circ_19264,RMVar_hsa_circ_254757,RMVar_hsa_circ_87603,RMVar_hsa_circ_312922,RMVar_hsa_circ_254755,RMVar_hsa_circ_254756,RMVar_hsa_circ_50049,RMVar_hsa_circ_349698,RMVar_hsa_circ_313275,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_254763,RMVar_hsa_circ_254764,RMVar_hsa_circ_254762,RMVar_hsa_circ_254759,RMVar_hsa_circ_254760,RMVar_hsa_circ_254758,RMVar_hsa_circ_254775,RMVar_hsa_circ_298297,RMVar_hsa_circ_254769,RMVar_hsa_circ_330673,RMVar_hsa_circ_332870,RMVar_hsa_circ_322670,RMVar_hsa_circ_48253,RMVar_hsa_circ_49484,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_292962,RMVar_hsa_circ_275014,RMVar_hsa_circ_254777,RMVar_hsa_circ_254776,RMVar_hsa_circ_28404,RMVar_hsa_circ_5209,RMVar_hsa_circ_254773,RMVar_hsa_circ_254774,RMVar_hsa_circ_280042,RMVar_hsa_circ_348271,RMVar_hsa_circ_344085,RMVar_hsa_circ_282877,RMVar_hsa_circ_254781,RMVar_hsa_circ_298072,RMVar_hsa_circ_319301,RMVar_hsa_circ_293225,RMVar_hsa_circ_283910,RMVar_hsa_circ_273049,RMVar_hsa_circ_280533,RMVar_hsa_circ_53314,RMVar_hsa_circ_254784,RMVar_hsa_circ_254786,RMVar_hsa_circ_254788,RMVar_hsa_circ_21231,RMVar_hsa_circ_254787,RMVar_hsa_circ_254785,RMVar_hsa_circ_254783,RMVar_hsa_circ_93272,RMVar_hsa_circ_254789 10332 RMVar_ID_10332 Human_SNP_ID_385203575 A-to-I Human chr8 - 140820118 140820114 140820119 TCCAGTCTGGGCGACAGAGTGAGACCCTATTTAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA TCCAGTCTGGGCGACAGAGTGAGACCCTATT_____AAAAAAAAAAAAAAAAAAAAAAAAAAAAA TTTTTA T PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232862084 Functional Loss DEL dbSNP153 32..36 33 - - - RMVar_hsa_circ_101087,RMVar_hsa_circ_254695,RMVar_hsa_circ_119341,RMVar_hsa_circ_9428,RMVar_hsa_circ_254700,RMVar_hsa_circ_63815,RMVar_hsa_circ_6314,RMVar_hsa_circ_254703,RMVar_hsa_circ_120136,RMVar_hsa_circ_108356,RMVar_hsa_circ_355294,RMVar_hsa_circ_254707,RMVar_hsa_circ_334369,RMVar_hsa_circ_103169,RMVar_hsa_circ_62254,RMVar_hsa_circ_43746,RMVar_hsa_circ_254709,RMVar_hsa_circ_355189,RMVar_hsa_circ_372200,RMVar_hsa_circ_324678,RMVar_hsa_circ_322054,RMVar_hsa_circ_100311,RMVar_hsa_circ_55128,RMVar_hsa_circ_254710,RMVar_hsa_circ_254711,RMVar_hsa_circ_254720,RMVar_hsa_circ_79843,RMVar_hsa_circ_293517,RMVar_hsa_circ_50439,RMVar_hsa_circ_34510,RMVar_hsa_circ_16409,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_54342,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_254745,RMVar_hsa_circ_349832,RMVar_hsa_circ_254744,RMVar_hsa_circ_347878,RMVar_hsa_circ_332346,RMVar_hsa_circ_294257,RMVar_hsa_circ_288942,RMVar_hsa_circ_19264,RMVar_hsa_circ_254757,RMVar_hsa_circ_87603,RMVar_hsa_circ_312922,RMVar_hsa_circ_254755,RMVar_hsa_circ_254756,RMVar_hsa_circ_50049,RMVar_hsa_circ_349698,RMVar_hsa_circ_313275,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_254763,RMVar_hsa_circ_254764,RMVar_hsa_circ_254762,RMVar_hsa_circ_254759,RMVar_hsa_circ_254760,RMVar_hsa_circ_254758,RMVar_hsa_circ_254775,RMVar_hsa_circ_298297,RMVar_hsa_circ_254769,RMVar_hsa_circ_330673,RMVar_hsa_circ_332870,RMVar_hsa_circ_322670,RMVar_hsa_circ_48253,RMVar_hsa_circ_49484,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_292962,RMVar_hsa_circ_275014,RMVar_hsa_circ_254777,RMVar_hsa_circ_254776,RMVar_hsa_circ_28404,RMVar_hsa_circ_5209,RMVar_hsa_circ_254773,RMVar_hsa_circ_254774,RMVar_hsa_circ_280042,RMVar_hsa_circ_348271,RMVar_hsa_circ_344085,RMVar_hsa_circ_282877,RMVar_hsa_circ_254781,RMVar_hsa_circ_298072,RMVar_hsa_circ_319301,RMVar_hsa_circ_293225,RMVar_hsa_circ_283910,RMVar_hsa_circ_273049,RMVar_hsa_circ_280533,RMVar_hsa_circ_53314,RMVar_hsa_circ_254784,RMVar_hsa_circ_254786,RMVar_hsa_circ_254788,RMVar_hsa_circ_21231,RMVar_hsa_circ_254787,RMVar_hsa_circ_254785,RMVar_hsa_circ_254783,RMVar_hsa_circ_93272,RMVar_hsa_circ_254789 10333 RMVar_ID_10333 Human_SNP_ID_385203576 A-to-I Human chr8 - 140820118 140820115 140820119 TCCAGTCTGGGCGACAGAGTGAGACCCTATTTAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA TCCAGTCTGGGCGACAGAGTGAGACCCTATT____AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA TTTTA T PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs372960207 Functional Loss DEL dbSNP153 32..35 33 - - - RMVar_hsa_circ_101087,RMVar_hsa_circ_254695,RMVar_hsa_circ_119341,RMVar_hsa_circ_9428,RMVar_hsa_circ_254700,RMVar_hsa_circ_63815,RMVar_hsa_circ_6314,RMVar_hsa_circ_254703,RMVar_hsa_circ_120136,RMVar_hsa_circ_108356,RMVar_hsa_circ_355294,RMVar_hsa_circ_254707,RMVar_hsa_circ_334369,RMVar_hsa_circ_103169,RMVar_hsa_circ_62254,RMVar_hsa_circ_43746,RMVar_hsa_circ_254709,RMVar_hsa_circ_355189,RMVar_hsa_circ_372200,RMVar_hsa_circ_324678,RMVar_hsa_circ_322054,RMVar_hsa_circ_100311,RMVar_hsa_circ_55128,RMVar_hsa_circ_254710,RMVar_hsa_circ_254711,RMVar_hsa_circ_254720,RMVar_hsa_circ_79843,RMVar_hsa_circ_293517,RMVar_hsa_circ_50439,RMVar_hsa_circ_34510,RMVar_hsa_circ_16409,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_54342,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_254745,RMVar_hsa_circ_349832,RMVar_hsa_circ_254744,RMVar_hsa_circ_347878,RMVar_hsa_circ_332346,RMVar_hsa_circ_294257,RMVar_hsa_circ_288942,RMVar_hsa_circ_19264,RMVar_hsa_circ_254757,RMVar_hsa_circ_87603,RMVar_hsa_circ_312922,RMVar_hsa_circ_254755,RMVar_hsa_circ_254756,RMVar_hsa_circ_50049,RMVar_hsa_circ_349698,RMVar_hsa_circ_313275,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_254763,RMVar_hsa_circ_254764,RMVar_hsa_circ_254762,RMVar_hsa_circ_254759,RMVar_hsa_circ_254760,RMVar_hsa_circ_254758,RMVar_hsa_circ_254775,RMVar_hsa_circ_298297,RMVar_hsa_circ_254769,RMVar_hsa_circ_330673,RMVar_hsa_circ_332870,RMVar_hsa_circ_322670,RMVar_hsa_circ_48253,RMVar_hsa_circ_49484,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_292962,RMVar_hsa_circ_275014,RMVar_hsa_circ_254777,RMVar_hsa_circ_254776,RMVar_hsa_circ_28404,RMVar_hsa_circ_5209,RMVar_hsa_circ_254773,RMVar_hsa_circ_254774,RMVar_hsa_circ_280042,RMVar_hsa_circ_348271,RMVar_hsa_circ_344085,RMVar_hsa_circ_282877,RMVar_hsa_circ_254781,RMVar_hsa_circ_298072,RMVar_hsa_circ_319301,RMVar_hsa_circ_293225,RMVar_hsa_circ_283910,RMVar_hsa_circ_273049,RMVar_hsa_circ_280533,RMVar_hsa_circ_53314,RMVar_hsa_circ_254784,RMVar_hsa_circ_254786,RMVar_hsa_circ_254788,RMVar_hsa_circ_21231,RMVar_hsa_circ_254787,RMVar_hsa_circ_254785,RMVar_hsa_circ_254783,RMVar_hsa_circ_93272,RMVar_hsa_circ_254789 10334 RMVar_ID_10334 Human_SNP_ID_385203578 A-to-I Human chr8 - 140820118 140820116 140820119 TCCAGTCTGGGCGACAGAGTGAGACCCTATTTAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA TCCAGTCTGGGCGACAGAGTGAGACCCTATT___AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA TTTA T PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1440803612 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_101087,RMVar_hsa_circ_254695,RMVar_hsa_circ_119341,RMVar_hsa_circ_9428,RMVar_hsa_circ_254700,RMVar_hsa_circ_63815,RMVar_hsa_circ_6314,RMVar_hsa_circ_254703,RMVar_hsa_circ_120136,RMVar_hsa_circ_108356,RMVar_hsa_circ_355294,RMVar_hsa_circ_254707,RMVar_hsa_circ_334369,RMVar_hsa_circ_103169,RMVar_hsa_circ_62254,RMVar_hsa_circ_43746,RMVar_hsa_circ_254709,RMVar_hsa_circ_355189,RMVar_hsa_circ_372200,RMVar_hsa_circ_324678,RMVar_hsa_circ_322054,RMVar_hsa_circ_100311,RMVar_hsa_circ_55128,RMVar_hsa_circ_254710,RMVar_hsa_circ_254711,RMVar_hsa_circ_254720,RMVar_hsa_circ_79843,RMVar_hsa_circ_293517,RMVar_hsa_circ_50439,RMVar_hsa_circ_34510,RMVar_hsa_circ_16409,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_54342,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_254745,RMVar_hsa_circ_349832,RMVar_hsa_circ_254744,RMVar_hsa_circ_347878,RMVar_hsa_circ_332346,RMVar_hsa_circ_294257,RMVar_hsa_circ_288942,RMVar_hsa_circ_19264,RMVar_hsa_circ_254757,RMVar_hsa_circ_87603,RMVar_hsa_circ_312922,RMVar_hsa_circ_254755,RMVar_hsa_circ_254756,RMVar_hsa_circ_50049,RMVar_hsa_circ_349698,RMVar_hsa_circ_313275,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_254763,RMVar_hsa_circ_254764,RMVar_hsa_circ_254762,RMVar_hsa_circ_254759,RMVar_hsa_circ_254760,RMVar_hsa_circ_254758,RMVar_hsa_circ_254775,RMVar_hsa_circ_298297,RMVar_hsa_circ_254769,RMVar_hsa_circ_330673,RMVar_hsa_circ_332870,RMVar_hsa_circ_322670,RMVar_hsa_circ_48253,RMVar_hsa_circ_49484,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_292962,RMVar_hsa_circ_275014,RMVar_hsa_circ_254777,RMVar_hsa_circ_254776,RMVar_hsa_circ_28404,RMVar_hsa_circ_5209,RMVar_hsa_circ_254773,RMVar_hsa_circ_254774,RMVar_hsa_circ_280042,RMVar_hsa_circ_348271,RMVar_hsa_circ_344085,RMVar_hsa_circ_282877,RMVar_hsa_circ_254781,RMVar_hsa_circ_298072,RMVar_hsa_circ_319301,RMVar_hsa_circ_293225,RMVar_hsa_circ_283910,RMVar_hsa_circ_273049,RMVar_hsa_circ_280533,RMVar_hsa_circ_53314,RMVar_hsa_circ_254784,RMVar_hsa_circ_254786,RMVar_hsa_circ_254788,RMVar_hsa_circ_21231,RMVar_hsa_circ_254787,RMVar_hsa_circ_254785,RMVar_hsa_circ_254783,RMVar_hsa_circ_93272,RMVar_hsa_circ_254789 10335 RMVar_ID_10335 Human_SNP_ID_385203579 A-to-I Human chr8 - 140820118 140820117 140820119 TCCAGTCTGGGCGACAGAGTGAGACCCTATTTAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA TCCAGTCTGGGCGACAGAGTGAGACCCTATT__AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA TTA T PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1566993197 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_101087,RMVar_hsa_circ_254695,RMVar_hsa_circ_119341,RMVar_hsa_circ_9428,RMVar_hsa_circ_254700,RMVar_hsa_circ_63815,RMVar_hsa_circ_6314,RMVar_hsa_circ_254703,RMVar_hsa_circ_120136,RMVar_hsa_circ_108356,RMVar_hsa_circ_355294,RMVar_hsa_circ_254707,RMVar_hsa_circ_334369,RMVar_hsa_circ_103169,RMVar_hsa_circ_62254,RMVar_hsa_circ_43746,RMVar_hsa_circ_254709,RMVar_hsa_circ_355189,RMVar_hsa_circ_372200,RMVar_hsa_circ_324678,RMVar_hsa_circ_322054,RMVar_hsa_circ_100311,RMVar_hsa_circ_55128,RMVar_hsa_circ_254710,RMVar_hsa_circ_254711,RMVar_hsa_circ_254720,RMVar_hsa_circ_79843,RMVar_hsa_circ_293517,RMVar_hsa_circ_50439,RMVar_hsa_circ_34510,RMVar_hsa_circ_16409,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_54342,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_254745,RMVar_hsa_circ_349832,RMVar_hsa_circ_254744,RMVar_hsa_circ_347878,RMVar_hsa_circ_332346,RMVar_hsa_circ_294257,RMVar_hsa_circ_288942,RMVar_hsa_circ_19264,RMVar_hsa_circ_254757,RMVar_hsa_circ_87603,RMVar_hsa_circ_312922,RMVar_hsa_circ_254755,RMVar_hsa_circ_254756,RMVar_hsa_circ_50049,RMVar_hsa_circ_349698,RMVar_hsa_circ_313275,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_254763,RMVar_hsa_circ_254764,RMVar_hsa_circ_254762,RMVar_hsa_circ_254759,RMVar_hsa_circ_254760,RMVar_hsa_circ_254758,RMVar_hsa_circ_254775,RMVar_hsa_circ_298297,RMVar_hsa_circ_254769,RMVar_hsa_circ_330673,RMVar_hsa_circ_332870,RMVar_hsa_circ_322670,RMVar_hsa_circ_48253,RMVar_hsa_circ_49484,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_292962,RMVar_hsa_circ_275014,RMVar_hsa_circ_254777,RMVar_hsa_circ_254776,RMVar_hsa_circ_28404,RMVar_hsa_circ_5209,RMVar_hsa_circ_254773,RMVar_hsa_circ_254774,RMVar_hsa_circ_280042,RMVar_hsa_circ_348271,RMVar_hsa_circ_344085,RMVar_hsa_circ_282877,RMVar_hsa_circ_254781,RMVar_hsa_circ_298072,RMVar_hsa_circ_319301,RMVar_hsa_circ_293225,RMVar_hsa_circ_283910,RMVar_hsa_circ_273049,RMVar_hsa_circ_280533,RMVar_hsa_circ_53314,RMVar_hsa_circ_254784,RMVar_hsa_circ_254786,RMVar_hsa_circ_254788,RMVar_hsa_circ_21231,RMVar_hsa_circ_254787,RMVar_hsa_circ_254785,RMVar_hsa_circ_254783,RMVar_hsa_circ_93272,RMVar_hsa_circ_254789 10336 RMVar_ID_10336 Human_SNP_ID_385203580 A-to-I Human chr8 - 140820118 140820118 140820118 TCCAGTCTGGGCGACAGAGTGAGACCCTATTTAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA TCCAGTCTGGGCGACAGAGTGAGACCCTATTTTAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA T A PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs951636923 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101087,RMVar_hsa_circ_254695,RMVar_hsa_circ_119341,RMVar_hsa_circ_9428,RMVar_hsa_circ_254700,RMVar_hsa_circ_63815,RMVar_hsa_circ_6314,RMVar_hsa_circ_254703,RMVar_hsa_circ_120136,RMVar_hsa_circ_108356,RMVar_hsa_circ_355294,RMVar_hsa_circ_254707,RMVar_hsa_circ_334369,RMVar_hsa_circ_103169,RMVar_hsa_circ_62254,RMVar_hsa_circ_43746,RMVar_hsa_circ_254709,RMVar_hsa_circ_355189,RMVar_hsa_circ_372200,RMVar_hsa_circ_324678,RMVar_hsa_circ_322054,RMVar_hsa_circ_100311,RMVar_hsa_circ_55128,RMVar_hsa_circ_254710,RMVar_hsa_circ_254711,RMVar_hsa_circ_254720,RMVar_hsa_circ_79843,RMVar_hsa_circ_293517,RMVar_hsa_circ_50439,RMVar_hsa_circ_34510,RMVar_hsa_circ_16409,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_54342,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_254745,RMVar_hsa_circ_349832,RMVar_hsa_circ_254744,RMVar_hsa_circ_347878,RMVar_hsa_circ_332346,RMVar_hsa_circ_294257,RMVar_hsa_circ_288942,RMVar_hsa_circ_19264,RMVar_hsa_circ_254757,RMVar_hsa_circ_87603,RMVar_hsa_circ_312922,RMVar_hsa_circ_254755,RMVar_hsa_circ_254756,RMVar_hsa_circ_50049,RMVar_hsa_circ_349698,RMVar_hsa_circ_313275,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_254763,RMVar_hsa_circ_254764,RMVar_hsa_circ_254762,RMVar_hsa_circ_254759,RMVar_hsa_circ_254760,RMVar_hsa_circ_254758,RMVar_hsa_circ_254775,RMVar_hsa_circ_298297,RMVar_hsa_circ_254769,RMVar_hsa_circ_330673,RMVar_hsa_circ_332870,RMVar_hsa_circ_322670,RMVar_hsa_circ_48253,RMVar_hsa_circ_49484,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_292962,RMVar_hsa_circ_275014,RMVar_hsa_circ_254777,RMVar_hsa_circ_254776,RMVar_hsa_circ_28404,RMVar_hsa_circ_5209,RMVar_hsa_circ_254773,RMVar_hsa_circ_254774,RMVar_hsa_circ_280042,RMVar_hsa_circ_348271,RMVar_hsa_circ_344085,RMVar_hsa_circ_282877,RMVar_hsa_circ_254781,RMVar_hsa_circ_298072,RMVar_hsa_circ_319301,RMVar_hsa_circ_293225,RMVar_hsa_circ_283910,RMVar_hsa_circ_273049,RMVar_hsa_circ_280533,RMVar_hsa_circ_53314,RMVar_hsa_circ_254784,RMVar_hsa_circ_254786,RMVar_hsa_circ_254788,RMVar_hsa_circ_21231,RMVar_hsa_circ_254787,RMVar_hsa_circ_254785,RMVar_hsa_circ_254783,RMVar_hsa_circ_93272,RMVar_hsa_circ_254789 10337 RMVar_ID_10337 Human_SNP_ID_385213642 A-to-I Human chr8 - 140861263 140861263 140861263 CTCACTGCAGCCTTGAACTTCTGGGCTCAAGCAATCGCCCTGCCTCAGCCTCCTGAGTAGTTGGG CTCACTGCAGCCTTGAACTTCTGGGCTCAAGCGATCGCCCTGCCTCAGCCTCCTGAGTAGTTGGG T C PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1370474168 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 10338 RMVar_ID_10338 Human_SNP_ID_385216547 A-to-I Human chr8 - 140873586 140873586 140873586 TGGCGGACGTCTGTAATCCCAGCTACTGGGGAAGCTGAAGCAGGAGAATCGCTTGAACCTGGGAG TGGCGGACGTCTGTAATCCCAGCTACTGGGGAGGCTGAAGCAGGAGAATCGCTTGAACCTGGGAG T C PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs912441926 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_254709,RMVar_hsa_circ_355189,RMVar_hsa_circ_324678,RMVar_hsa_circ_322054,RMVar_hsa_circ_254720,RMVar_hsa_circ_79843,RMVar_hsa_circ_293517,RMVar_hsa_circ_34510,RMVar_hsa_circ_2596,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_77007,RMVar_hsa_circ_286767,RMVar_hsa_circ_305313,RMVar_hsa_circ_254744,RMVar_hsa_circ_332346,RMVar_hsa_circ_288942,RMVar_hsa_circ_19264,RMVar_hsa_circ_254757,RMVar_hsa_circ_254756,RMVar_hsa_circ_349698,RMVar_hsa_circ_286717,RMVar_hsa_circ_311942,RMVar_hsa_circ_290687,RMVar_hsa_circ_279729,RMVar_hsa_circ_1973,RMVar_hsa_circ_254759,RMVar_hsa_circ_254760,RMVar_hsa_circ_254758,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_28404,RMVar_hsa_circ_5209,RMVar_hsa_circ_254773,RMVar_hsa_circ_254774,RMVar_hsa_circ_280042,RMVar_hsa_circ_282877,RMVar_hsa_circ_254781,RMVar_hsa_circ_319301,RMVar_hsa_circ_293225,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_93272,RMVar_hsa_circ_254795,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_284623,RMVar_hsa_circ_297776,RMVar_hsa_circ_364237,RMVar_hsa_circ_286215,RMVar_hsa_circ_278354,RMVar_hsa_circ_254797,RMVar_hsa_circ_254798,RMVar_hsa_circ_254796,RMVar_hsa_circ_254804,RMVar_hsa_circ_270852,RMVar_hsa_circ_254801,RMVar_hsa_circ_280309,RMVar_hsa_circ_314660,RMVar_hsa_circ_355911,RMVar_hsa_circ_254802,RMVar_hsa_circ_322669,RMVar_hsa_circ_328876,RMVar_hsa_circ_333595,RMVar_hsa_circ_274966,RMVar_hsa_circ_254806,RMVar_hsa_circ_254805,RMVar_hsa_circ_254807 10339 RMVar_ID_10339 Human_SNP_ID_385217733 A-to-I Human chr8 - 140878550 140878550 140878550 TCGCCCTGTCACCCAGGCTGCAGTACGGTGGCATGAACATGGCTCACTGCAGCCTCTTGGGCTCA TCGCCCTGTCACCCAGGCTGCAGTACGGTGGCGTGAACATGGCTCACTGCAGCCTCTTGGGCTCA T C PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs993172363 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_254709,RMVar_hsa_circ_355189,RMVar_hsa_circ_324678,RMVar_hsa_circ_322054,RMVar_hsa_circ_254720,RMVar_hsa_circ_79843,RMVar_hsa_circ_293517,RMVar_hsa_circ_34510,RMVar_hsa_circ_2596,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_77007,RMVar_hsa_circ_286767,RMVar_hsa_circ_305313,RMVar_hsa_circ_254744,RMVar_hsa_circ_332346,RMVar_hsa_circ_288942,RMVar_hsa_circ_19264,RMVar_hsa_circ_254757,RMVar_hsa_circ_254756,RMVar_hsa_circ_349698,RMVar_hsa_circ_286717,RMVar_hsa_circ_311942,RMVar_hsa_circ_290687,RMVar_hsa_circ_279729,RMVar_hsa_circ_1973,RMVar_hsa_circ_254759,RMVar_hsa_circ_254760,RMVar_hsa_circ_254758,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_28404,RMVar_hsa_circ_5209,RMVar_hsa_circ_254773,RMVar_hsa_circ_254774,RMVar_hsa_circ_280042,RMVar_hsa_circ_282877,RMVar_hsa_circ_254781,RMVar_hsa_circ_319301,RMVar_hsa_circ_293225,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_93272,RMVar_hsa_circ_254795,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_284623,RMVar_hsa_circ_297776,RMVar_hsa_circ_364237,RMVar_hsa_circ_286215,RMVar_hsa_circ_278354,RMVar_hsa_circ_254797,RMVar_hsa_circ_254798,RMVar_hsa_circ_254796,RMVar_hsa_circ_254804,RMVar_hsa_circ_270852,RMVar_hsa_circ_254801,RMVar_hsa_circ_280309,RMVar_hsa_circ_314660,RMVar_hsa_circ_355911,RMVar_hsa_circ_254802,RMVar_hsa_circ_322669,RMVar_hsa_circ_328876,RMVar_hsa_circ_333595,RMVar_hsa_circ_274966,RMVar_hsa_circ_254806,RMVar_hsa_circ_254805,RMVar_hsa_circ_254808 10340 RMVar_ID_10340 Human_SNP_ID_385217738 A-to-I Human chr8 - 140878558 140878558 140878558 ACAGAGTCTCGCCCTGTCACCCAGGCTGCAGTACGGTGGCATGAACATGGCTCACTGCAGCCTCT ACAGAGTCTCGCCCTGTCACCCAGGCTGCAGTGCGGTGGCATGAACATGGCTCACTGCAGCCTCT T C PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1430740402 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26155691 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_254709,RMVar_hsa_circ_355189,RMVar_hsa_circ_324678,RMVar_hsa_circ_322054,RMVar_hsa_circ_254720,RMVar_hsa_circ_79843,RMVar_hsa_circ_293517,RMVar_hsa_circ_34510,RMVar_hsa_circ_2596,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_77007,RMVar_hsa_circ_286767,RMVar_hsa_circ_305313,RMVar_hsa_circ_254744,RMVar_hsa_circ_332346,RMVar_hsa_circ_288942,RMVar_hsa_circ_19264,RMVar_hsa_circ_254757,RMVar_hsa_circ_254756,RMVar_hsa_circ_349698,RMVar_hsa_circ_286717,RMVar_hsa_circ_311942,RMVar_hsa_circ_290687,RMVar_hsa_circ_279729,RMVar_hsa_circ_1973,RMVar_hsa_circ_254759,RMVar_hsa_circ_254760,RMVar_hsa_circ_254758,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_28404,RMVar_hsa_circ_5209,RMVar_hsa_circ_254773,RMVar_hsa_circ_254774,RMVar_hsa_circ_280042,RMVar_hsa_circ_282877,RMVar_hsa_circ_254781,RMVar_hsa_circ_319301,RMVar_hsa_circ_293225,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_93272,RMVar_hsa_circ_254795,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_284623,RMVar_hsa_circ_297776,RMVar_hsa_circ_364237,RMVar_hsa_circ_286215,RMVar_hsa_circ_278354,RMVar_hsa_circ_254797,RMVar_hsa_circ_254798,RMVar_hsa_circ_254796,RMVar_hsa_circ_254804,RMVar_hsa_circ_270852,RMVar_hsa_circ_254801,RMVar_hsa_circ_280309,RMVar_hsa_circ_314660,RMVar_hsa_circ_355911,RMVar_hsa_circ_254802,RMVar_hsa_circ_322669,RMVar_hsa_circ_328876,RMVar_hsa_circ_333595,RMVar_hsa_circ_274966,RMVar_hsa_circ_254806,RMVar_hsa_circ_254805,RMVar_hsa_circ_254808 10341 RMVar_ID_10341 Human_SNP_ID_385227920 A-to-I Human chr8 - 140918011 140918011 140918011 TATGCTTGGCACATACTAGGTGTTTGTTAAATATTTGTTGAATGAATCAATGACTAGTGTGCACA TATGCTTGGCACATACTAGGTGTTTGTTAAATGTTTGTTGAATGAATCAATGACTAGTGTGCACA T C PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934606198 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3146354,Human_RBP_ID_16375174 RMVar_hsa_circ_101087,RMVar_hsa_circ_254695,RMVar_hsa_circ_108356,RMVar_hsa_circ_355294,RMVar_hsa_circ_254707,RMVar_hsa_circ_103169,RMVar_hsa_circ_254709,RMVar_hsa_circ_324678,RMVar_hsa_circ_2596,RMVar_hsa_circ_14253,RMVar_hsa_circ_342408,RMVar_hsa_circ_376365,RMVar_hsa_circ_298567,RMVar_hsa_circ_254734,RMVar_hsa_circ_305313,RMVar_hsa_circ_19264,RMVar_hsa_circ_254757,RMVar_hsa_circ_311942,RMVar_hsa_circ_290687,RMVar_hsa_circ_1973,RMVar_hsa_circ_254758,RMVar_hsa_circ_357556,RMVar_hsa_circ_309613,RMVar_hsa_circ_5209,RMVar_hsa_circ_319301,RMVar_hsa_circ_293225,RMVar_hsa_circ_53314,RMVar_hsa_circ_254788,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_254794,RMVar_hsa_circ_284623,RMVar_hsa_circ_297776,RMVar_hsa_circ_254796,RMVar_hsa_circ_270852,RMVar_hsa_circ_355911,RMVar_hsa_circ_322669,RMVar_hsa_circ_254806,RMVar_hsa_circ_273424,RMVar_hsa_circ_311931,RMVar_hsa_circ_254809,RMVar_hsa_circ_254810,RMVar_hsa_circ_316559,RMVar_hsa_circ_18344 10342 RMVar_ID_10342 Human_SNP_ID_385232470 A-to-I Human chr8 - 140936054 140936054 140936054 CTCCTGTCTCAGCCTCCTGAGTAGCCGGGACTACAGATGCATGCCACCATGCCTGGCTTATTTTT CTCCTGTCTCAGCCTCCTGAGTAGCCGGGACTGCAGATGCATGCCACCATGCCTGGCTTATTTTT T C PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559981966 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1973,RMVar_hsa_circ_53314,RMVar_hsa_circ_122662,RMVar_hsa_circ_10234,RMVar_hsa_circ_254809 10343 RMVar_ID_10343 Human_SNP_ID_385237580 A-to-I Human chr8 - 140957306 140957306 140957306 CTCCCACCTCAGCTTCCCAAGTAGCTGAGACTACATGCGTGTGCCACCATGCCCAGCTAATTTTT CTCCCACCTCAGCTTCCCAAGTAGCTGAGACTGCATGCGTGTGCCACCATGCCCAGCTAATTTTT T C PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1433661246 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122662,RMVar_hsa_circ_254809 10344 RMVar_ID_10344 Human_SNP_ID_385238430 A-to-I Human chr8 - 140960503 140960496 140960504 ACTTATTCTTTTTTTAAGGGTTAAAATGGGCCAGCCGCGGTGGCTCATACCTGTAATCCCAACAC ACTTATTCTTTTTTTAAGGGTTAAAATGGGC________GTGGCTCATACCTGTAATCCCAACAC CCGCGGCTG C PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1370765047 Functional Loss DEL dbSNP153 32..39 33 - - - RMVar_hsa_circ_122662,RMVar_hsa_circ_254809 10345 RMVar_ID_10345 Human_SNP_ID_385238437 A-to-I Human chr8 - 140960503 140960503 140960503 ACTTATTCTTTTTTTAAGGGTTAAAATGGGCCAGCCGCGGTGGCTCATACCTGTAATCCCAACAC ACTTATTCTTTTTTTAAGGGTTAAAATGGGCCCGCCGCGGTGGCTCATACCTGTAATCCCAACAC T G PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1176429348 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122662,RMVar_hsa_circ_254809 10346 RMVar_ID_10346 Human_SNP_ID_385239062 A-to-I Human chr8 - 140962609 140962609 140962609 TTTTTTGTATTTTTAGTAGGTTTCACTGTGTTAGCCAGGATGGTCTCGATCTCCTCACCTCATGA TTTTTTGTATTTTTAGTAGGTTTCACTGTGTTGGCCAGGATGGTCTCGATCTCCTCACCTCATGA T C PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1331432689 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122662,RMVar_hsa_circ_254809 10347 RMVar_ID_10347 Human_SNP_ID_385245372 A-to-I Human chr8 - 140987821 140987821 140987821 GCAGGCTGGTGTCAAACTCCTGTGCTCAAGCAATCCTCCAGTCTTGGCATTCCAAAGTGCTGGGG GCAGGCTGGTGTCAAACTCCTGTGCTCAAGCAGTCCTCCAGTCTTGGCATTCCAAAGTGCTGGGG T C PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs750353988 Functional Loss SNV dbSNP153 33..33 33 - - - 10348 RMVar_ID_10348 Human_SNP_ID_385247049 A-to-I Human chr8 - 140993985 140993985 140993985 TAACTCACACCTGTAATTCCACCACTTTGGGAAGCCGAGGTGGACAGATCGCTTGAGCCCAGGAG TAACTCACACCTGTAATTCCACCACTTTGGGAGGCCGAGGTGGACAGATCGCTTGAGCCCAGGAG T C PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1362036298 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3146608 10349 RMVar_ID_10349 Human_SNP_ID_385286012 A-to-I Human chr8 + 141141852 141141852 141141852 ACTGCTTGAGCCGAGGGGTTTGAGACAAGCCTAGGGAACATAGCAATACCCTGTCTCTAAAAAAC ACTGCTTGAGCCGAGGGGTTTGAGACAAGCCTGGGGAACATAGCAATACCCTGTCTCTAAAAAAC A G DENND3 Ensembl:ENSG00000105339 Protein coding 3'UTR GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs992396576 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_270333 RMVar_hsa_circ_267044,RMVar_hsa_circ_348026,RMVar_hsa_circ_254819,RMVar_hsa_circ_56983,RMVar_hsa_circ_300378,RMVar_hsa_circ_339219,RMVar_hsa_circ_254820 10350 RMVar_ID_10350 Human_SNP_ID_385286021 A-to-I Human chr8 + 141141890 141141890 141141890 CATAGCAATACCCTGTCTCTAAAAAACAATTTAAAAACTAGTTGGGCATGGTGGTGTGTGCCTGT CATAGCAATACCCTGTCTCTAAAAAACAATTTGAAAACTAGTTGGGCATGGTGGTGTGTGCCTGT A G DENND3 Ensembl:ENSG00000105339 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1383070869 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267044,RMVar_hsa_circ_348026,RMVar_hsa_circ_254819,RMVar_hsa_circ_56983,RMVar_hsa_circ_300378,RMVar_hsa_circ_339219,RMVar_hsa_circ_254820 10351 RMVar_ID_10351 Human_SNP_ID_385286024 A-to-I Human chr8 + 141141897 141141897 141141897 ATACCCTGTCTCTAAAAAACAATTTAAAAACTAGTTGGGCATGGTGGTGTGTGCCTGTAGTCCCA ATACCCTGTCTCTAAAAAACAATTTAAAAACTGGTTGGGCATGGTGGTGTGTGCCTGTAGTCCCA A G DENND3 Ensembl:ENSG00000105339 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1412633641 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267044,RMVar_hsa_circ_348026,RMVar_hsa_circ_254819,RMVar_hsa_circ_56983,RMVar_hsa_circ_300378,RMVar_hsa_circ_339219,RMVar_hsa_circ_254820 10352 RMVar_ID_10352 Human_SNP_ID_385286432 A-to-I Human chr8 + 141143606 141143606 141143606 TTTAAATTTTTTGTAGAGACGGGGGTCTCACTATCTTGCGCAGGCTGGCCTTGAACTCCTGGCCT TTTAAATTTTTTGTAGAGACGGGGGTCTCACTGTCTTGCGCAGGCTGGCCTTGAACTCCTGGCCT A G DENND3 Ensembl:ENSG00000105339 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984417007 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267044,RMVar_hsa_circ_348026,RMVar_hsa_circ_254819,RMVar_hsa_circ_56983,RMVar_hsa_circ_300378,RMVar_hsa_circ_339219,RMVar_hsa_circ_254820 10353 RMVar_ID_10353 Human_SNP_ID_385297846 A-to-I Human chr8 + 141185807 141185806 141185808 AGATCGCGCCACTGCACTCCAGCCTGGGTGACAGAGCCATACCCTGTCTCAAACAGACAAATAAT AGATCGCGCCACTGCACTCCAGCCTGGGTGAC__AGCCATACCCTGTCTCAAACAGACAAATAAT CAG C DENND3 Ensembl:ENSG00000105339 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1255178795 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_340381,RMVar_hsa_circ_1429,RMVar_hsa_circ_254826,RMVar_hsa_circ_42059,RMVar_hsa_circ_53873,RMVar_hsa_circ_48208,RMVar_hsa_circ_254842,RMVar_hsa_circ_337662,RMVar_hsa_circ_362540,RMVar_hsa_circ_312648,RMVar_hsa_circ_254841 10354 RMVar_ID_10354 Human_SNP_ID_385717010 A-to-I Human chr8 - 142612222 142612222 142612222 AGCTCCAGTGATTCACGCCCGCCTGGAGAAGAATCAGAGCTCAGCTCATGACTCACCCATGGCAG AGCTCCAGTGATTCACGCCCGCCTGGAGAAGAGTCAGAGCTCAGCTCATGACTCACCCATGGCAG T C ARC Ensembl:ENSG00000198576 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1423792688 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1018018,Human_Splice_Rec_1018022 RMVar_hsa_circ_102131,RMVar_hsa_circ_118970,RMVar_hsa_circ_254870,RMVar_hsa_circ_254871 10355 RMVar_ID_10355 Human_SNP_ID_385730009 A-to-I Human chr8 - 142660524 142660524 142660524 GTGGTGGCATGTGCCTGTAACCCCAGCTACTCAGGAGGCCGAGGCGGGAGGATCCCCAAGCCCAG GTGGTGGCATGTGCCTGTAACCCCAGCTACTCGGGAGGCCGAGGCGGGAGGATCCCCAAGCCCAG T C JRK Ensembl:ENSG00000234616 Protein coding 3'UTR GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs978890542 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7817266,Human_RBP_ID_26558746 10356 RMVar_ID_10356 Human_SNP_ID_385730738 A-to-I Human chr8 - 142663139 142663135 142663139 ATTGTCCTTTTCTTTTCTTGAGGCAGGGTCTCACTCTGTTGACCAGGCTGGAGTGAAGTGGTGTG ATTGTCCTTTTCTTTTCTTGAGGCAGGGTCTC____TGTTGACCAGGCTGGAGTGAAGTGGTGTG AGAGT A JRK Ensembl:ENSG00000234616 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1300403591 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_16377447 10357 RMVar_ID_10357 Human_SNP_ID_385732633 A-to-I Human chr8 + 142668010 142668010 142668010 GTTAAGACACTGCTGAGGGTGGTGAGGGCTGAAAAGCTGTTTGCCCAAACACCGGGCAGCTCAGC GTTAAGACACTGCTGAGGGTGGTGAGGGCTGACAAGCTGTTTGCCCAAACACCGGGCAGCTCAGC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs782414754 Functional Loss SNV dbSNP153 33..33 33 - - - 10358 RMVar_ID_10358 Human_SNP_ID_385732812 A-to-I Human chr8 - 142668617 142668617 142668617 GAGCTGTGTCTGGTGTTGAGTCTCCTCCAGGAAGCTTTTCTCTGCATCCCAGTCCCCAGTTAGTC GAGCTGTGTCTGGTGTTGAGTCTCCTCCAGGACGCTTTTCTCTGCATCCCAGTCCCCAGTTAGTC T G JRK Ensembl:ENSG00000234616 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1554636654 Functional Loss SNV dbSNP153 33..33 33 - - - 10359 RMVar_ID_10359 Human_SNP_ID_385837287 A-to-I Human chr8 + 143045917 143045917 143045917 TCACTGTTACCCAAGCTGGAGTACAGTGGCACAGTCTTGGCTCACTGCAACCTCTGCTTCCCAGG TCACTGTTACCCAAGCTGGAGTACAGTGGCACGGTCTTGGCTCACTGCAACCTCTGCTTCCCAGG A G C8orf31 Ensembl:ENSG00000177335 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs894118910 Functional Loss SNV dbSNP153 33..33 33 - - - 10360 RMVar_ID_10360 Human_SNP_ID_385837315 A-to-I Human chr8 + 143046036 143046036 143046036 CCACCACACCCAGTTAATTTTTGTATATTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGG CCACCACACCCAGTTAATTTTTGTATATTAGTGGAGATGGGGTTTCACCATGTTGGCCAGGCTGG A G C8orf31 Ensembl:ENSG00000177335 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs751496488 Functional Loss SNV dbSNP153 33..33 33 - - - 10361 RMVar_ID_10361 Human_SNP_ID_385837351 A-to-I Human chr8 + 143046209 143046209 143046209 GGCAGCAGGTGGGCCTGGTGGCTCACATCTGTAATCTCATCACTTTGGGAGGCCAAGGCAGGAAG GGCAGCAGGTGGGCCTGGTGGCTCACATCTGTGATCTCATCACTTTGGGAGGCCAAGGCAGGAAG A G C8orf31 Ensembl:ENSG00000177335 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs758537371 Functional Loss SNV dbSNP153 33..33 33 - - - 10362 RMVar_ID_10362 Human_SNP_ID_385837398 A-to-I Human chr8 + 143046389 143046389 143046389 CACAAGGTCAGGAGATCGAGACCATCCTGCCTAACATAGTGAAACCCCATCTTTACTAAAACTAC CACAAGGTCAGGAGATCGAGACCATCCTGCCTGACATAGTGAAACCCCATCTTTACTAAAACTAC A G C8orf31 Ensembl:ENSG00000177335 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1038852243 Functional Loss SNV dbSNP153 33..33 33 - - - 10363 RMVar_ID_10363 Human_SNP_ID_385837421 A-to-I Human chr8 + 143046467 143046467 143046467 GGGCGTGGTGGCAGGTGCCTGTAGTCCCAGCTACTTGGGAGGCTAAGGCAGGAGAATGGCATGAA GGGCGTGGTGGCAGGTGCCTGTAGTCCCAGCTGCTTGGGAGGCTAAGGCAGGAGAATGGCATGAA A G C8orf31 Ensembl:ENSG00000177335 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1348890874 Functional Loss SNV dbSNP153 33..33 33 - - - 10364 RMVar_ID_10364 Human_SNP_ID_385838442 A-to-I Human chr8 + 143050245 143050245 143050245 GCTCTGTCACCAAGCTGGAGTGCAGTGGTGTGATCTCGACTCACTGCAACCTTTGCCTCCCGGGT GCTCTGTCACCAAGCTGGAGTGCAGTGGTGTGGTCTCGACTCACTGCAACCTTTGCCTCCCGGGT A G C8orf31 Ensembl:ENSG00000177335 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs999255633 Functional Loss SNV dbSNP153 33..33 33 - - - 10365 RMVar_ID_10365 Human_SNP_ID_385838486 A-to-I Human chr8 + 143050433 143050433 143050433 AAACTCCTGACCTAAAGTGACCCACCCGTCTCAGCCTCCTAAAGTGCTGGGATTACAGGAGTGAG AAACTCCTGACCTAAAGTGACCCACCCGTCTCGGCCTCCTAAAGTGCTGGGATTACAGGAGTGAG A G C8orf31 Ensembl:ENSG00000177335 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs559685647 Functional Loss SNV dbSNP153 33..33 33 - - - 10366 RMVar_ID_10366 Human_SNP_ID_385838487 A-to-I Human chr8 + 143050433 143050433 143050433 AAACTCCTGACCTAAAGTGACCCACCCGTCTCAGCCTCCTAAAGTGCTGGGATTACAGGAGTGAG AAACTCCTGACCTAAAGTGACCCACCCGTCTCTGCCTCCTAAAGTGCTGGGATTACAGGAGTGAG A T C8orf31 Ensembl:ENSG00000177335 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs559685647 Functional Loss SNV dbSNP153 33..33 33 - - - 10367 RMVar_ID_10367 Human_SNP_ID_385838642 A-to-I Human chr8 + 143051051 143051051 143051051 TGCAAGGAAATCCCCCATTACATATGCAAAAGAAATACTGCGGCTTTTAGAGGCTGTGCAGGAGC TGCAAGGAAATCCCCCATTACATATGCAAAAGCAATACTGCGGCTTTTAGAGGCTGTGCAGGAGC A C C8orf31 Ensembl:ENSG00000177335 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1563919922 Functional Loss SNV dbSNP153 33..33 33 - - - 10368 RMVar_ID_10368 Human_SNP_ID_385838755 A-to-I Human chr8 + 143051490 143051490 143051490 TTGAACTGGGGAGGCAGAGGTTGCAGCGACCCAAGATCGCACCATTGCACTCCAGCCTGGGTGAC TTGAACTGGGGAGGCAGAGGTTGCAGCGACCCGAGATCGCACCATTGCACTCCAGCCTGGGTGAC A G C8orf31 Ensembl:ENSG00000177335 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs576038015 Functional Loss SNV dbSNP153 33..33 33 - - - 10369 RMVar_ID_10369 Human_SNP_ID_385901619 A-to-I Human chr8 + 143265150 143265150 143265150 AAGTTGGTGAGCGCCTGTAGTCCCAGCTACTCAGGACGGTGAGGCAGGAGAATAGCATGAATCCG AAGTTGGTGAGCGCCTGTAGTCCCAGCTACTCGGGACGGTGAGGCAGGAGAATAGCATGAATCCG A G AC138696.1 Ensembl:ENSG00000264668 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005330289 Functional Loss SNV dbSNP153 33..33 33 - - - 10370 RMVar_ID_10370 Human_SNP_ID_385911065 A-to-I Human chr8 + 143295394 143295394 143295394 AATTCTATTTTTTTAAGAGACAGGATCTCACTATGTTGGCCAGGCTGGTCTTGAACTCCAAGTCT AATTCTATTTTTTTAAGAGACAGGATCTCACTGTGTTGGCCAGGCTGGTCTTGAACTCCAAGTCT A G ZNF696 Ensembl:ENSG00000185730 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs997906970 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1018658,Human_Splice_Rec_1018659 10371 RMVar_ID_10371 Human_SNP_ID_385911091 A-to-I Human chr8 + 143295467 143295462 143295468 CCTCCTGCCTCAGCCTCTGAAAGTGCGGAGATACAGGTGTGAGTCACCACATCCGGCCCCACAGC CCTCCTGCCTCAGCCTCTGAAAGTGCGG______AGGTGTGAGTCACCACATCCGGCCCCACAGC GAGATAC G ZNF696 Ensembl:ENSG00000185730 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs759349613 Functional Loss DEL dbSNP153 29..34 33 - - - Human_Splice_Rec_1018658,Human_Splice_Rec_1018659 10372 RMVar_ID_10372 Human_SNP_ID_385911092 A-to-I Human chr8 + 143295467 143295467 143295467 CCTCCTGCCTCAGCCTCTGAAAGTGCGGAGATACAGGTGTGAGTCACCACATCCGGCCCCACAGC CCTCCTGCCTCAGCCTCTGAAAGTGCGGAGATTCAGGTGTGAGTCACCACATCCGGCCCCACAGC A T ZNF696 Ensembl:ENSG00000185730 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1314942952 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1018658,Human_Splice_Rec_1018659 10373 RMVar_ID_10373 Human_SNP_ID_385914292 A-to-I Human chr8 + 143305179 143305179 143305179 TCCAACCTCAGCCCCACGGGTAGCTTGAGACTACAGGCGCGCACCACCATGCCCAGCTAATTTTG TCCAACCTCAGCCCCACGGGTAGCTTGAGACTTCAGGCGCGCACCACCATGCCCAGCTAATTTTG A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs897587103 Functional Loss SNV dbSNP153 33..33 33 - - - 10374 RMVar_ID_10374 Human_SNP_ID_385916631 A-to-I Human chr8 + 143311189 143311189 143311189 CAGGGTTTCACCATGTTGGCCATGATGGTCTCAAACTCCCAACCTCAAGTGATCTGCCTGCCTCG CAGGGTTTCACCATGTTGGCCATGATGGTCTCTAACTCCCAACCTCAAGTGATCTGCCTGCCTCG A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1189693521 Functional Loss SNV dbSNP153 33..33 33 - - - 10375 RMVar_ID_10375 Human_SNP_ID_385916734 A-to-I Human chr8 - 143311694 143311694 143311694 TTGCCCAGGCTGGAGTGCAGTGGCATGATCTCAGCTCACCACAACCTCTGCCTCCCGGGTTCAAA TTGCCCAGGCTGGAGTGCAGTGGCATGATCTCCGCTCACCACAACCTCTGCCTCCCGGGTTCAAA T G TOP1MT Ensembl:ENSG00000184428 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1234739490 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64222,RMVar_hsa_circ_81378,RMVar_hsa_circ_254890 10376 RMVar_ID_10376 Human_SNP_ID_385922459 A-to-I Human chr8 - 143324069 143324069 143324069 GCGGGGATTTGTGGACGAGATCCGCTCCCAGTACCGGGCTGACTGGAAGTCTCGGGAAATGAAGA GCGGGGATTTGTGGACGAGATCCGCTCCCAGTTCCGGGCTGACTGGAAGTCTCGGGAAATGAAGA T A TOP1MT Ensembl:ENSG00000184428 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs969037830 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_695455,Human_RBP_ID_959455,Human_RBP_ID_3974134,Human_RBP_ID_18125130,Human_RBP_ID_19023103,Human_RBP_ID_26360195 Human_Splice_Rec_1018678,Human_Splice_Rec_1018679,Human_Splice_Rec_1018708,Human_Splice_Rec_1018709,Human_Splice_Rec_1018734,Human_Splice_Rec_1018735,Human_Splice_Rec_1018762,Human_Splice_Rec_1018763,Human_Splice_Rec_1018788,Human_Splice_Rec_1018789,Human_Splice_Rec_1018806,Human_Splice_Rec_1018807,Human_Splice_Rec_1018824,Human_Splice_Rec_1018838 Human_miRNA_ID_2577223 RMVar_hsa_circ_53775,RMVar_hsa_circ_64222,RMVar_hsa_circ_109666,RMVar_hsa_circ_254891 10377 RMVar_ID_10377 Human_SNP_ID_385922460 A-to-I Human chr8 - 143324069 143324069 143324069 GCGGGGATTTGTGGACGAGATCCGCTCCCAGTACCGGGCTGACTGGAAGTCTCGGGAAATGAAGA GCGGGGATTTGTGGACGAGATCCGCTCCCAGTCCCGGGCTGACTGGAAGTCTCGGGAAATGAAGA T G TOP1MT Ensembl:ENSG00000184428 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs969037830 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_695455,Human_RBP_ID_959455,Human_RBP_ID_3974134,Human_RBP_ID_18125130,Human_RBP_ID_19023103,Human_RBP_ID_26360195 Human_Splice_Rec_1018678,Human_Splice_Rec_1018679,Human_Splice_Rec_1018708,Human_Splice_Rec_1018709,Human_Splice_Rec_1018734,Human_Splice_Rec_1018735,Human_Splice_Rec_1018762,Human_Splice_Rec_1018763,Human_Splice_Rec_1018788,Human_Splice_Rec_1018789,Human_Splice_Rec_1018806,Human_Splice_Rec_1018807,Human_Splice_Rec_1018824,Human_Splice_Rec_1018838 Human_miRNA_ID_2577223 RMVar_hsa_circ_53775,RMVar_hsa_circ_64222,RMVar_hsa_circ_109666,RMVar_hsa_circ_254891 10378 RMVar_ID_10378 Human_SNP_ID_385992528 A-to-I Human chr8 + 143557501 143557461 143557501 ATGATGCCGCTGTGACGACGGATGCTGCCACTATGGCGAAGGATGCTGCCGTGAACTTTGGTGCA _________________________________TGGCGAAGGATGCTGCCGTGAACTTTGGTGCA GATGAAGGATGATGCCGCTGTGACGACGGATGCTGCCACTA G GSDMD Ensembl:ENSG00000104518 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1398175521 Functional Loss DEL dbSNP153 1..33 33 - - - 10379 RMVar_ID_10379 Human_SNP_ID_385992566 A-to-I Human chr8 + 143557501 143557501 143557501 ATGATGCCGCTGTGACGACGGATGCTGCCACTATGGCGAAGGATGCTGCCGTGAACTTTGGTGCA ATGATGCCGCTGTGACGACGGATGCTGCCACTGTGGCGAAGGATGCTGCCGTGAACTTTGGTGCA A G GSDMD Ensembl:ENSG00000104518 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs879061281 Functional Loss SNV dbSNP153 33..33 33 - - - 10380 RMVar_ID_10380 Human_SNP_ID_385992567 A-to-I Human chr8 + 143557501 143557501 143557501 ATGATGCCGCTGTGACGACGGATGCTGCCACTATGGCGAAGGATGCTGCCGTGAACTTTGGTGCA ATGATGCCGCTGTGACGACGGATGCTGCCACTTTGGCGAAGGATGCTGCCGTGAACTTTGGTGCA A T GSDMD Ensembl:ENSG00000104518 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs879061281 Functional Loss SNV dbSNP153 33..33 33 - - - 10381 RMVar_ID_10381 Human_SNP_ID_386006098 A-to-I Human chr8 - 143590700 143590700 143590700 CAGGGTTTCAACGTGTTAGCCAGGATGGTCTCAGTCTCCAGACCCTGTGATCCGCCCGCCTCGGC CAGGGTTTCAACGTGTTAGCCAGGATGGTCTCGGTCTCCAGACCCTGTGATCCGCCCGCCTCGGC T C EEF1D Ensembl:ENSG00000104529 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1463992442 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1693863,Human_RBP_ID_4973097,Human_RBP_ID_16378961,Human_RBP_ID_18893162,Human_RBP_ID_26156261 Human_Splice_Rec_1019546,Human_Splice_Rec_1019547,Human_Splice_Rec_1019848,Human_Splice_Rec_1019849,Human_Splice_Rec_1019851,Human_Splice_Rec_1019854,Human_Splice_Rec_1019855,Human_Splice_Rec_1019860,Human_Splice_Rec_1019861,Human_Splice_Rec_1019864,Human_Splice_Rec_1019865,Human_Splice_Rec_1019878,Human_Splice_Rec_1019879,Human_Splice_Rec_1019882,Human_Splice_Rec_1019883,Human_Splice_Rec_1019886,Human_Splice_Rec_1019887,Human_Splice_Rec_1019890,Human_Splice_Rec_1019891,Human_Splice_Rec_1019898,Human_Splice_Rec_1019899 10382 RMVar_ID_10382 Human_SNP_ID_386006105 A-to-I Human chr8 - 143590731 143590730 143590732 GGCTAATTTTTATTTTTATTTTTAGTAGAGACAGGGTTTCAACGTGTTAGCCAGGATGGTCTCAG GGCTAATTTTTATTTTTATTTTTAGTAGAGA__GGGTTTCAACGTGTTAGCCAGGATGGTCTCAG CTG C EEF1D Ensembl:ENSG00000104529 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1458280039 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_3178245,Human_RBP_ID_16378970 Human_Splice_Rec_1019546,Human_Splice_Rec_1019854,Human_Splice_Rec_1019860,Human_Splice_Rec_1019861,Human_Splice_Rec_1019864,Human_Splice_Rec_1019878,Human_Splice_Rec_1019882,Human_Splice_Rec_1019883,Human_Splice_Rec_1019886,Human_Splice_Rec_1019890,Human_Splice_Rec_1019898 10383 RMVar_ID_10383 Human_SNP_ID_386014017 A-to-I Human chr8 - 143613594 143613594 143613594 CCTGACCCGGTGGCTCCCCACAGTGGGCGAGGAAGATGAGGTCTCCATCAAGGAGGCAGCCGAGG CCTGACCCGGTGGCTCCCCACAGTGGGCGAGGCAGATGAGGTCTCCATCAAGGAGGCAGCCGAGG T G TSTA3 Ensembl:ENSG00000104522 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs372009690 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_254779,Human_RBP_ID_959480,Human_RBP_ID_1054637,Human_RBP_ID_3147058,Human_RBP_ID_3973389,Human_RBP_ID_5405507,Human_RBP_ID_19022230,Human_RBP_ID_19140445,Human_RBP_ID_23259509,Human_RBP_ID_27831604 Human_Splice_Rec_1019977,Human_Splice_Rec_1019981,Human_Splice_Rec_1020000,Human_Splice_Rec_1020001,Human_Splice_Rec_1020016,Human_Splice_Rec_1020017,Human_Splice_Rec_1020036,Human_Splice_Rec_1020037,Human_Splice_Rec_1020058 Human_miRNA_ID_3079620 RMVar_hsa_circ_85140,RMVar_hsa_circ_93878,RMVar_hsa_circ_254913,RMVar_hsa_circ_254914 10384 RMVar_ID_10384 Human_SNP_ID_386021042 A-to-I Human chr8 + 143638948 143638948 143638948 GAGGTTTGCTCTTGTTGCCCAGGCTGGAGTGCAATGGCGCGATCTCAGCTCATTCCACCCTCTGC GAGGTTTGCTCTTGTTGCCCAGGCTGGAGTGCGATGGCGCGATCTCAGCTCATTCCACCCTCTGC A G ZNF623 Ensembl:ENSG00000183309 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1292557588 Functional Loss SNV dbSNP153 33..33 33 - - - 10385 RMVar_ID_10385 Human_SNP_ID_386021138 A-to-I Human chr8 + 143639287 143639287 143639287 TTGCCCAGGCTGGAGTGCAATGGCGTGATCTCAGCTCACTGCAGCCTCCACCTCCGCCTCCTGGG TTGCCCAGGCTGGAGTGCAATGGCGTGATCTCGGCTCACTGCAGCCTCCACCTCCGCCTCCTGGG A G ZNF623 Ensembl:ENSG00000183309 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041614823 Functional Loss SNV dbSNP153 33..33 33 - - - 10386 RMVar_ID_10386 Human_SNP_ID_386021504 A-to-I Human chr8 + 143640820 143640820 143640820 AAAATTAGCTGGGCGTGGTGGCGCACTCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA AAAATTAGCTGGGCGTGGTGGCGCACTCCTGTGATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA A G ZNF623 Ensembl:ENSG00000183309 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs898185988 Functional Loss SNV dbSNP153 33..33 33 - - - 10387 RMVar_ID_10387 Human_SNP_ID_386022412 A-to-I Human chr8 + 143644195 143644195 143644195 GGTGCATGCCACCACACCTGGATAATTTTTGTATTTTTAGTAGAGATGAGGTTTCACCATAGCCA GGTGCATGCCACCACACCTGGATAATTTTTGTGTTTTTAGTAGAGATGAGGTTTCACCATAGCCA A G ZNF623 Ensembl:ENSG00000183309 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1053276458 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16379515 10388 RMVar_ID_10388 Human_SNP_ID_386022830 A-to-I Human chr8 + 143645357 143645357 143645357 CCAGTTGCTCGGCAGGAGAATGGCGTGAACCCAGGAGGCAGAGCCTGCAGTGAGCTGAGATGGCG CCAGTTGCTCGGCAGGAGAATGGCGTGAACCCGGGAGGCAGAGCCTGCAGTGAGCTGAGATGGCG A G ZNF623 Ensembl:ENSG00000183309 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs929260671 Functional Loss SNV dbSNP153 33..33 33 - - - 10389 RMVar_ID_10389 Human_SNP_ID_386022832 A-to-I Human chr8 + 143645364 143645364 143645364 CTCGGCAGGAGAATGGCGTGAACCCAGGAGGCAGAGCCTGCAGTGAGCTGAGATGGCGCCACTGC CTCGGCAGGAGAATGGCGTGAACCCAGGAGGCGGAGCCTGCAGTGAGCTGAGATGGCGCCACTGC A G ZNF623 Ensembl:ENSG00000183309 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1254129732 Functional Loss SNV dbSNP153 33..33 33 - - - 10390 RMVar_ID_10390 Human_SNP_ID_386025674 A-to-I Human chr8 + 143655473 143655473 143655473 GGGACTGTAGGCATGCATCACCACATCTTGCTAATTTTTTATATTTTTTTGTAGAGATGGGGGTC GGGACTGTAGGCATGCATCACCACATCTTGCTGATTTTTTATATTTTTTTGTAGAGATGGGGGTC A G ZNF623 Ensembl:ENSG00000183309 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1019016361 Functional Loss SNV dbSNP153 33..33 33 - - - 10391 RMVar_ID_10391 Human_SNP_ID_386025676 A-to-I Human chr8 + 143655481 143655481 143655481 AGGCATGCATCACCACATCTTGCTAATTTTTTATATTTTTTTGTAGAGATGGGGGTCTCACTATG AGGCATGCATCACCACATCTTGCTAATTTTTTGTATTTTTTTGTAGAGATGGGGGTCTCACTATG A G ZNF623 Ensembl:ENSG00000183309 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs770981903 Functional Loss SNV dbSNP153 33..33 33 - - - 10392 RMVar_ID_10392 Human_SNP_ID_386025682 A-to-I Human chr8 + 143655493 143655493 143655493 CCACATCTTGCTAATTTTTTATATTTTTTTGTAGAGATGGGGGTCTCACTATGTTGACCAGGCTG CCACATCTTGCTAATTTTTTATATTTTTTTGTGGAGATGGGGGTCTCACTATGTTGACCAGGCTG A G ZNF623 Ensembl:ENSG00000183309 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1287586677 Functional Loss SNV dbSNP153 33..33 33 - - - 10393 RMVar_ID_10393 Human_SNP_ID_386034561 A-to-I Human chr8 + 143685451 143685450 143685451 GGGAGGCTGAGGCAAGAGAATCGTTTGAACCCAAGAGGCAGAGGTTGCAGTGAGCAGAGATCGCG GGGAGGCTGAGGCAAGAGAATCGTTTGAACCC_AGAGGCAGAGGTTGCAGTGAGCAGAGATCGCG CA C ZNF707 Ensembl:ENSG00000181135 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs568552559 Functional Loss DEL dbSNP153 33..33 33 - - - 10394 RMVar_ID_10394 Human_SNP_ID_386035194 A-to-I Human chr8 + 143687538 143687538 143687538 TTGTATTTTTAGTAGAGACAGGGTTTTGCCATATTGGCCAGACTGGTCTCAAACTCCCCACCTCA TTGTATTTTTAGTAGAGACAGGGTTTTGCCATGTTGGCCAGACTGGTCTCAAACTCCCCACCTCA A G ZNF707 Ensembl:ENSG00000181135 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1554612459 Functional Loss SNV dbSNP153 33..33 33 - - - 10395 RMVar_ID_10395 Human_SNP_ID_386090568 A-to-I Human chr8 - 143851215 143851215 143851215 CCTCAGCCTCCCAAAGTGCTGGAATTACAGACATGAGCCGGCACGTCTGGCCTATATTCTGATTT CCTCAGCCTCCCAAAGTGCTGGAATTACAGACGTGAGCCGGCACGTCTGGCCTATATTCTGATTT T C lnc-EPPK1-2 RNACentral:URS0000D5BCBE lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432732233 Functional Loss SNV dbSNP153 33..33 33 - - - 10396 RMVar_ID_10396 Human_SNP_ID_386090590 A-to-I Human chr8 - 143851295 143851295 143851295 CCCAGCAGATTTTGTAGAGCTGGGGTTTCGCCATGTTGCCTAGGCTGGTCTTGAACTCCTGAGCT CCCAGCAGATTTTGTAGAGCTGGGGTTTCGCCGTGTTGCCTAGGCTGGTCTTGAACTCCTGAGCT T C lnc-EPPK1-2 RNACentral:URS0000D5BCBE lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334291068 Functional Loss SNV dbSNP153 33..33 33 - - - 10397 RMVar_ID_10397 Human_SNP_ID_386090625 A-to-I Human chr8 - 143851452 143851452 143851452 CAGGTTGGAGTGCAGTGGTACAACAGCTCACTACAGCCTCGAACTCCTGGGCTCAAGCGATCCTT CAGGTTGGAGTGCAGTGGTACAACAGCTCACTGCAGCCTCGAACTCCTGGGCTCAAGCGATCCTT T C lnc-EPPK1-2 RNACentral:URS0000D5BCBE lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1390754126 Functional Loss SNV dbSNP153 33..33 33 - - - 10398 RMVar_ID_10398 Human_SNP_ID_386091530 A-to-I Human chr8 - 143854760 143854760 143854760 CCAAGAAGTGGAGGTTGCAGTGAGCCAAGATCACACCATTGCACTCCAGCCTGAGCAACAGAGTG CCAAGAAGTGGAGGTTGCAGTGAGCCAAGATCGCACCATTGCACTCCAGCCTGAGCAACAGAGTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1142547 Functional Loss SNV dbSNP153 33..33 33 - - - 10399 RMVar_ID_10399 Human_SNP_ID_386125716 A-to-I Human chr8 - 143943231 143943231 143943231 ATGGGGCGGGGCCCTGGGGATTGGGCAGCCTCAATTATGGGCTTCTGGCCAGAGGGACTGCCTAT ATGGGGCGGGGCCCTGGGGATTGGGCAGCCTCCATTATGGGCTTCTGGCCAGAGGGACTGCCTAT T G PLEC Ensembl:ENSG00000178209 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1234114792 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80124,RMVar_hsa_circ_254971,RMVar_hsa_circ_116464,RMVar_hsa_circ_254996 10400 RMVar_ID_10400 Human_SNP_ID_386130185 A-to-I Human chr8 - 143955827 143955827 143955827 AGCACTGGGAGGTGGGAGGATTGCTTGAGCCCAGGAGTTTGAGACCAGCCTGGGCAACACAGAGA AGCACTGGGAGGTGGGAGGATTGCTTGAGCCCGGGAGTTTGAGACCAGCCTGGGCAACACAGAGA T C PLEC Ensembl:ENSG00000178209 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1402064653 Functional Loss SNV dbSNP153 33..33 33 - - - 10401 RMVar_ID_10401 Human_SNP_ID_386130374 A-to-I Human chr8 - 143956522 143956522 143956522 TTGCTCTCTCCCAGACAGGAATGCAGTGGCGCAATCACGGCTCACTGCAGCCTTGGGTGGGCTGG TTGCTCTCTCCCAGACAGGAATGCAGTGGCGCCATCACGGCTCACTGCAGCCTTGGGTGGGCTGG T G PLEC Ensembl:ENSG00000178209 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs578018017 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8155172 10402 RMVar_ID_10402 Human_SNP_ID_386131744 A-to-I Human chr8 - 143961363 143961363 143961363 AAATTAGCAGGGTGTGGTGGTGCACGCCTGTAATCCCCGCTACGCAGGAGGCTGAGGCAGGAGAA AAATTAGCAGGGTGTGGTGGTGCACGCCTGTAGTCCCCGCTACGCAGGAGGCTGAGGCAGGAGAA T C PLEC Ensembl:ENSG00000178209 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1554740829 Functional Loss SNV dbSNP153 33..33 33 - - - 10403 RMVar_ID_10403 Human_SNP_ID_386180789 A-to-I Human chr8 + 144117755 144117754 144117755 CTCCTTCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCATGTGCCACCACGCCCAGCTAATTTTG CTCCTTCCTCAGCCTCCTGAGTAGCTGGGATT_CAGGCATGTGCCACCACGCCCAGCTAATTTTG TA T WDR97 Ensembl:ENSG00000179698 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1303686937 Functional Loss DEL dbSNP153 33..33 33 - - - 10404 RMVar_ID_10404 Human_SNP_ID_386180792 A-to-I Human chr8 + 144117761 144117761 144117761 CCTCAGCCTCCTGAGTAGCTGGGATTACAGGCATGTGCCACCACGCCCAGCTAATTTTGTATTTT CCTCAGCCTCCTGAGTAGCTGGGATTACAGGCGTGTGCCACCACGCCCAGCTAATTTTGTATTTT A G WDR97 Ensembl:ENSG00000179698 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs534162778 Functional Loss SNV dbSNP153 33..33 33 - - - 10405 RMVar_ID_10405 Human_SNP_ID_386199745 A-to-I Human chr8 + 144186234 144186234 144186234 CCTCTTGCCTCCCAGGCTGAAGTGATCCTCCCACCTCAGCTCCCAGAGTAGCTGCGACCAGAGGT CCTCTTGCCTCCCAGGCTGAAGTGATCCTCCCGCCTCAGCTCCCAGAGTAGCTGCGACCAGAGGT A G MROH1 Ensembl:ENSG00000179832 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1176987862 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 10406 RMVar_ID_10406 Human_SNP_ID_386199901 A-to-I Human chr8 + 144186835 144186835 144186835 TCAGGCTAGGCCGGGCGCGGTGGCTCACGCCTATAATCCTAGCACTTTGGGAGGCTGAGGCAGGC TCAGGCTAGGCCGGGCGCGGTGGCTCACGCCTCTAATCCTAGCACTTTGGGAGGCTGAGGCAGGC A C MROH1 Ensembl:ENSG00000179832 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1213561218 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 10407 RMVar_ID_10407 Human_SNP_ID_386207405 A-to-I Human chr8 + 144212834 144212834 144212834 ACTGATCTTGAGCTCCTGATCTCAAGTGATCCACCTGCCCCGGCCTCCCAAAGTGTTGGGATTAC ACTGATCTTGAGCTCCTGATCTCAAGTGATCCGCCTGCCCCGGCCTCCCAAAGTGTTGGGATTAC A G MROH1 Ensembl:ENSG00000179832 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1011082528 Functional Loss SNV dbSNP153 33..33 33 - - - 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 10408 RMVar_ID_10408 Human_SNP_ID_386211583 A-to-I Human chr8 + 144227474 144227474 144227474 CAAAACCAGCCTGGACAATCTGGCGAAACCCCATTTCCACAAAAAATACAAAAATTAGCTGGGTA CAAAACCAGCCTGGACAATCTGGCGAAACCCCCTTTCCACAAAAAATACAAAAATTAGCTGGGTA A C MROH1 Ensembl:ENSG00000179832 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1231536202 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47501,RMVar_hsa_circ_112785,RMVar_hsa_circ_76813,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 10409 RMVar_ID_10409 Human_SNP_ID_386231260 A-to-I Human chr8 + 144293635 144293635 144293635 GATTGTTGTATTTTTAGTAGAGACGGGGTTTCACCACATTGGACAGGCTGGTCTGGAACTCCTGA GATTGTTGTATTTTTAGTAGAGACGGGGTTTCTCCACATTGGACAGGCTGGTCTGGAACTCCTGA A T HSF1 Ensembl:ENSG00000185122 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1482231062 Functional Loss SNV dbSNP153 33..33 33 - - - 10410 RMVar_ID_10410 Human_SNP_ID_386231264 A-to-I Human chr8 + 144293647 144293645 144293648 TTTAGTAGAGACGGGGTTTCACCACATTGGACAGGCTGGTCTGGAACTCCTGACCTCAAGTTATC TTTAGTAGAGACGGGGTTTCACCACATTGGA___GCTGGTCTGGAACTCCTGACCTCAAGTTATC ACAG A HSF1 Ensembl:ENSG00000185122 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223478129 Functional Loss DEL dbSNP153 32..34 33 - - - 10411 RMVar_ID_10411 Human_SNP_ID_386231266 A-to-I Human chr8 + 144293647 144293647 144293647 TTTAGTAGAGACGGGGTTTCACCACATTGGACAGGCTGGTCTGGAACTCCTGACCTCAAGTTATC TTTAGTAGAGACGGGGTTTCACCACATTGGACTGGCTGGTCTGGAACTCCTGACCTCAAGTTATC A T HSF1 Ensembl:ENSG00000185122 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1344292949 Functional Loss SNV dbSNP153 33..33 33 - - - 10412 RMVar_ID_10412 Human_SNP_ID_386231827 A-to-I Human chr8 + 144295742 144295742 144295742 TGGCTTTTTTTTTTTTTTCTTTTTAAGGTTTTAGTAGAGACAGGGTCTCGCCGTATTGCCCAAGC TGGCTTTTTTTTTTTTTTCTTTTTAAGGTTTTTGTAGAGACAGGGTCTCGCCGTATTGCCCAAGC A T HSF1 Ensembl:ENSG00000185122 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1554841186 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3147349,Human_RBP_ID_16381197,Human_RBP_ID_18114126 10413 RMVar_ID_10413 Human_SNP_ID_386235331 A-to-I Human chr8 + 144307613 144307613 144307613 AATACAGAAATGAGCCGGGCGTGGTGGCGCCTATAGTCAGCTACTCGGGAGGCTGAGGCAGGAGA AATACAGAAATGAGCCGGGCGTGGTGGCGCCTGTAGTCAGCTACTCGGGAGGCTGAGGCAGGAGA A G HSF1 Ensembl:ENSG00000185122 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1342009979 Functional Loss SNV dbSNP153 33..33 33 - - - 10414 RMVar_ID_10414 Human_SNP_ID_386235333 A-to-I Human chr8 + 144307615 144307615 144307615 TACAGAAATGAGCCGGGCGTGGTGGCGCCTATAGTCAGCTACTCGGGAGGCTGAGGCAGGAGAAT TACAGAAATGAGCCGGGCGTGGTGGCGCCTATCGTCAGCTACTCGGGAGGCTGAGGCAGGAGAAT A C HSF1 Ensembl:ENSG00000185122 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1554843504 Functional Loss SNV dbSNP153 33..33 33 - - - 10415 RMVar_ID_10415 Human_SNP_ID_386235334 A-to-I Human chr8 + 144307615 144307615 144307615 TACAGAAATGAGCCGGGCGTGGTGGCGCCTATAGTCAGCTACTCGGGAGGCTGAGGCAGGAGAAT TACAGAAATGAGCCGGGCGTGGTGGCGCCTATTGTCAGCTACTCGGGAGGCTGAGGCAGGAGAAT A T HSF1 Ensembl:ENSG00000185122 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1554843504 Functional Loss SNV dbSNP153 33..33 33 - - - 10416 RMVar_ID_10416 Human_SNP_ID_386256216 A-to-I Human chr8 + 144365073 144365073 144365073 ATATCTACCAAAAAATTAAAAATTGGCTGGGCATGGTGGTGAGAGCCTACAGTCCCACTTACTCG ATATCTACCAAAAAATTAAAAATTGGCTGGGCGTGGTGGTGAGAGCCTACAGTCCCACTTACTCG A G RF00017-7378 RNACentral:URS00009554F6 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1263572412 Functional Loss SNV dbSNP153 33..33 33 - - - 10417 RMVar_ID_10417 Human_SNP_ID_386262219 A-to-I Human chr8 + 144386119 144386119 144386119 CAACCTCCATATCCCAGGTTCAAGCAATTCTCATGCTTCGGCCTCCCGAGTAGCTGGGACTACAG CAACCTCCATATCCCAGGTTCAAGCAATTCTCGTGCTTCGGCCTCCCGAGTAGCTGGGACTACAG A G ADCK5 Ensembl:ENSG00000173137 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232490006 Functional Loss SNV dbSNP153 33..33 33 - - - 10418 RMVar_ID_10418 Human_SNP_ID_386262732 A-to-I Human chr8 + 144388148 144388148 144388148 TTGGGAGGCCGAGGAGGGCGGATCACGAGGTCAGGAGTTCGAGACCAGCCTGACCAACGTGGAGA TTGGGAGGCCGAGGAGGGCGGATCACGAGGTCGGGAGTTCGAGACCAGCCTGACCAACGTGGAGA A G ADCK5 Ensembl:ENSG00000173137 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1310092719 Functional Loss SNV dbSNP153 33..33 33 - - - 10419 RMVar_ID_10419 Human_SNP_ID_386262738 A-to-I Human chr8 + 144388168 144388168 144388168 GATCACGAGGTCAGGAGTTCGAGACCAGCCTGACCAACGTGGAGAAACCCCATCTCTACTAAAGA GATCACGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACGTGGAGAAACCCCATCTCTACTAAAGA A G ADCK5 Ensembl:ENSG00000173137 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1409204266 Functional Loss SNV dbSNP153 33..33 33 - - - 10420 RMVar_ID_10420 Human_SNP_ID_386262956 A-to-I Human chr8 + 144388644 144388644 144388644 AAAATTAGCCGGGCGTGGTGTTGGGCGCCTGTAGTCCCAGCTACTCTGGAGGCTGAGGCAGGAGA AAAATTAGCCGGGCGTGGTGTTGGGCGCCTGTGGTCCCAGCTACTCTGGAGGCTGAGGCAGGAGA A G ADCK5 Ensembl:ENSG00000173137 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1480082942 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_181366 10421 RMVar_ID_10421 Human_SNP_ID_386262958 A-to-I Human chr8 + 144388654 144388654 144388654 GGGCGTGGTGTTGGGCGCCTGTAGTCCCAGCTACTCTGGAGGCTGAGGCAGGAGAACGGCGTGAA GGGCGTGGTGTTGGGCGCCTGTAGTCCCAGCTGCTCTGGAGGCTGAGGCAGGAGAACGGCGTGAA A G ADCK5 Ensembl:ENSG00000173137 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1206237175 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_181366 10422 RMVar_ID_10422 Human_SNP_ID_386262981 A-to-I Human chr8 + 144388714 144388714 144388714 GTGAACCTGGGAGGCGGAGCCTGCAGTGAGCCAAGATCGCCACCACACTCCAGCCTGGGCGACAG GTGAACCTGGGAGGCGGAGCCTGCAGTGAGCCGAGATCGCCACCACACTCCAGCCTGGGCGACAG A G ADCK5 Ensembl:ENSG00000173137 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1238316114 Functional Loss SNV dbSNP153 33..33 33 - - - 10423 RMVar_ID_10423 Human_SNP_ID_386266651 A-to-I Human chr8 - 144396685 144396685 144396685 GAGAAGAAGCCAAAGCCATCCAAGAAGAAAGCAGAAGGTGGCGGCGCAGAGGAGGGGGCTGGGGC GAGAAGAAGCCAAAGCCATCCAAGAAGAAAGCTGAAGGTGGCGGCGCAGAGGAGGGGGCTGGGGC T A CPSF1 Ensembl:ENSG00000071894 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs376334897 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_87948,Human_RBP_ID_4975123,Human_RBP_ID_22836599 Human_Splice_Rec_1024014,Human_Splice_Rec_1024015,Human_Splice_Rec_1024086,Human_Splice_Rec_1024087,Human_Splice_Rec_1024143 RMVar_hsa_circ_119874,RMVar_hsa_circ_255106,RMVar_hsa_circ_97961,RMVar_hsa_circ_255116,RMVar_hsa_circ_121767,RMVar_hsa_circ_255120 10424 RMVar_ID_10424 Human_SNP_ID_386266652 A-to-I Human chr8 - 144396685 144396685 144396685 GAGAAGAAGCCAAAGCCATCCAAGAAGAAAGCAGAAGGTGGCGGCGCAGAGGAGGGGGCTGGGGC GAGAAGAAGCCAAAGCCATCCAAGAAGAAAGCGGAAGGTGGCGGCGCAGAGGAGGGGGCTGGGGC T C CPSF1 Ensembl:ENSG00000071894 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs376334897 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_87948,Human_RBP_ID_4975123,Human_RBP_ID_22836599 Human_Splice_Rec_1024014,Human_Splice_Rec_1024015,Human_Splice_Rec_1024086,Human_Splice_Rec_1024087,Human_Splice_Rec_1024143 RMVar_hsa_circ_119874,RMVar_hsa_circ_255106,RMVar_hsa_circ_97961,RMVar_hsa_circ_255116,RMVar_hsa_circ_121767,RMVar_hsa_circ_255120 10425 RMVar_ID_10425 Human_SNP_ID_386270329 A-to-I Human chr8 - 144404962 144404962 144404962 CGGCTCACTGCAAGCTCCACCTCCTGGGTTCAAGCGATTCCCCTGCCTCAGCCTCCTGAGTAGCT CGGCTCACTGCAAGCTCCACCTCCTGGGTTCAGGCGATTCCCCTGCCTCAGCCTCCTGAGTAGCT T C CPSF1 Ensembl:ENSG00000071894 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1554868604 Functional Loss SNV dbSNP153 33..33 33 - - - 10426 RMVar_ID_10426 Human_SNP_ID_386275556 A-to-I Human chr8 + 144418909 144418909 144418909 TTAAGGCACCCTGAGTGGTGGTGGGTGCCTGTAGTCCCAGCGACTCGGGAGGCTGAGGCAGAATT TTAAGGCACCCTGAGTGGTGGTGGGTGCCTGTGGTCCCAGCGACTCGGGAGGCTGAGGCAGAATT A G lnc-ADCK5-4 RNACentral:URS0000D577E5 lincRNA intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1198477295 Functional Loss SNV dbSNP153 33..33 33 - - - 10427 RMVar_ID_10427 Human_SNP_ID_386302621 A-to-I Human chr8 - 144487152 144487152 144487152 AAACCCCGTCTCTACTAGAAATACAAAAAATTAGCCGGTTGTGGTGCCACACACCTGTAGTCCCA AAACCCCGTCTCTACTAGAAATACAAAAAATTTGCCGGTTGTGGTGCCACACACCTGTAGTCCCA T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1231333743 Functional Loss SNV dbSNP153 33..33 33 - - - 10428 RMVar_ID_10428 Human_SNP_ID_386307415 A-to-I Human chr8 + 144501533 144501533 144501533 GGACCTTCACTGCCCGCAGGAGGACAACCCCGAAGTGGTCAGGCCGCACAATGGCCGAGTAGGGG GGACCTTCACTGCCCGCAGGAGGACAACCCCGCAGTGGTCAGGCCGCACAATGGCCGAGTAGGGG A C PPP1R16A Ensembl:ENSG00000160972 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1247906676 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4996481,Human_RBP_ID_27831658 Human_Splice_Rec_1024770,Human_Splice_Rec_1024800,Human_Splice_Rec_1024826,Human_Splice_Rec_1024844 Human_miRNA_ID_2077024 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 10429 RMVar_ID_10429 Human_SNP_ID_386307416 A-to-I Human chr8 + 144501533 144501533 144501533 GGACCTTCACTGCCCGCAGGAGGACAACCCCGAAGTGGTCAGGCCGCACAATGGCCGAGTAGGGG GGACCTTCACTGCCCGCAGGAGGACAACCCCGGAGTGGTCAGGCCGCACAATGGCCGAGTAGGGG A G PPP1R16A Ensembl:ENSG00000160972 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1247906676 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4996481,Human_RBP_ID_27831658 Human_Splice_Rec_1024770,Human_Splice_Rec_1024800,Human_Splice_Rec_1024826,Human_Splice_Rec_1024844 Human_miRNA_ID_2077024 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 10430 RMVar_ID_10430 Human_SNP_ID_386325791 A-to-I Human chr8 - 144540705 144540705 144540705 GCCTCCACCTCTCAGGCTCGTGGGATCCTCCCACCTCAGCCTCCCGAGTAGCTGGGGCCACAGGC GCCTCCACCTCTCAGGCTCGTGGGATCCTCCCGCCTCAGCCTCCCGAGTAGCTGGGGCCACAGGC T C ARHGAP39 Ensembl:ENSG00000147799 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs372083381 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_255173,RMVar_hsa_circ_370610 10431 RMVar_ID_10431 Human_SNP_ID_386325876 A-to-I Human chr8 - 144540976 144540976 144540976 ATGGTGGCGGGCGCCTGTAATCCCAGGCACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCCA ATGGTGGCGGGCGCCTGTAATCCCAGGCACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCCA T C ARHGAP39 Ensembl:ENSG00000147799 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs540645087 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_255173,RMVar_hsa_circ_370610 10432 RMVar_ID_10432 Human_SNP_ID_386345896 A-to-I Human chr8 - 144604518 144604518 144604518 CAAAAATTAGCCAGATGTGGTGGCAGATGCCTATGGTCTCAGCTACTCGGGAGGCTGAGGTGAGG CAAAAATTAGCCAGATGTGGTGGCAGATGCCTGTGGTCTCAGCTACTCGGGAGGCTGAGGTGAGG T C ARHGAP39 Ensembl:ENSG00000147799 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs527658099 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_314579,RMVar_hsa_circ_292885 10433 RMVar_ID_10433 Human_SNP_ID_386377981 A-to-I Human chr8 - 144724469 144724469 144724469 TATTTTGGCTAGGCACAGTGGCCTGCACCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAAG TATTTTGGCTAGGCACAGTGGCCTGCACCTGTCGTCCCAGCTACTTGGGAGGCTGAGGCAGGAAG T G ZNF251 Ensembl:ENSG00000198169 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1274462695 Functional Loss SNV dbSNP153 33..33 33 - - - 10434 RMVar_ID_10434 Human_SNP_ID_386377984 A-to-I Human chr8 - 144724475 144724475 144724475 AAGTTATATTTTGGCTAGGCACAGTGGCCTGCACCTGTAGTCCCAGCTACTTGGGAGGCTGAGGC AAGTTATATTTTGGCTAGGCACAGTGGCCTGCGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGC T C ZNF251 Ensembl:ENSG00000198169 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1255265611 Functional Loss SNV dbSNP153 33..33 33 - - - 10435 RMVar_ID_10435 Human_SNP_ID_386381867 A-to-I Human chr8 - 144736783 144736783 144736783 TCAAAAATTAACAATAATAAAGTAGGCCGGGCACGGTGGCTCACGCCTGTAATCCCATCACTTTG TCAAAAATTAACAATAATAAAGTAGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCATCACTTTG T C ZNF251 Ensembl:ENSG00000198169 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1234039045 Functional Loss SNV dbSNP153 33..33 33 - - - 10436 RMVar_ID_10436 Human_SNP_ID_386381868 A-to-I Human chr8 - 144736783 144736783 144736783 TCAAAAATTAACAATAATAAAGTAGGCCGGGCACGGTGGCTCACGCCTGTAATCCCATCACTTTG TCAAAAATTAACAATAATAAAGTAGGCCGGGCCCGGTGGCTCACGCCTGTAATCCCATCACTTTG T G ZNF251 Ensembl:ENSG00000198169 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1234039045 Functional Loss SNV dbSNP153 33..33 33 - - - 10437 RMVar_ID_10437 Human_SNP_ID_386383086 A-to-I Human chr8 - 144740742 144740742 144740742 TTTAGTAGAGATGGGGTTTCACCATGTTGGTCAGGCTGGTCTCGAATTCCTGAGCTTAGGCAATC TTTAGTAGAGATGGGGTTTCACCATGTTGGTCGGGCTGGTCTCGAATTCCTGAGCTTAGGCAATC T C ZNF251 Ensembl:ENSG00000198169 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs753397937 Functional Loss SNV dbSNP153 33..33 33 - - - 10438 RMVar_ID_10438 Human_SNP_ID_386383087 A-to-I Human chr8 - 144740742 144740742 144740742 TTTAGTAGAGATGGGGTTTCACCATGTTGGTCAGGCTGGTCTCGAATTCCTGAGCTTAGGCAATC TTTAGTAGAGATGGGGTTTCACCATGTTGGTCCGGCTGGTCTCGAATTCCTGAGCTTAGGCAATC T G ZNF251 Ensembl:ENSG00000198169 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs753397937 Functional Loss SNV dbSNP153 33..33 33 - - - 10439 RMVar_ID_10439 Human_SNP_ID_386384227 A-to-I Human chr8 - 144744893 144744893 144744893 CGCCACCACGCCCAGCTGGTTTTTGTACTTTTAGTAGAGATGGGGTTTTGCCATGTTGGCCATGC CGCCACCACGCCCAGCTGGTTTTTGTACTTTTCGTAGAGATGGGGTTTTGCCATGTTGGCCATGC T G ZNF251 Ensembl:ENSG00000198169 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1410571086 Functional Loss SNV dbSNP153 33..33 33 - - - 10440 RMVar_ID_10440 Human_SNP_ID_386384474 A-to-I Human chr8 - 144745687 144745687 144745687 TTTTTGTTAGCTAGGCCTGGTGGCATGTGCCTATATTCCCAGCTATTTGGGAGGCTGAGGTGGGA TTTTTGTTAGCTAGGCCTGGTGGCATGTGCCTGTATTCCCAGCTATTTGGGAGGCTGAGGTGGGA T C ZNF251 Ensembl:ENSG00000198169 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs147077086 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16384099,Human_RBP_ID_23084198 10441 RMVar_ID_10441 Human_SNP_ID_386385252 A-to-I Human chr8 - 144748702 144748702 144748702 AAAAAATTAGCTTGGTGTGGTGTTGTGTACCTATAAGTCTCAGCTACTCAAGAGGCTGATGTGGT AAAAAATTAGCTTGGTGTGGTGTTGTGTACCTGTAAGTCTCAGCTACTCAAGAGGCTGATGTGGT T C ZNF251 Ensembl:ENSG00000198169 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1213626940 Functional Loss SNV dbSNP153 33..33 33 - - - 10442 RMVar_ID_10442 Human_SNP_ID_386385420 A-to-I Human chr8 - 144749363 144749363 144749363 CTCCCACCACAGCCTCCCAAGTAGCTGGGACTACAGGCATGTACTACCACACCTGGCTGATTTTT CTCCCACCACAGCCTCCCAAGTAGCTGGGACTGCAGGCATGTACTACCACACCTGGCTGATTTTT T C ZNF251 Ensembl:ENSG00000198169 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs367731171 Functional Loss SNV dbSNP153 33..33 33 - - - 10443 RMVar_ID_10443 Human_SNP_ID_386385425 A-to-I Human chr8 - 144749385 144749385 144749385 GACCTCCCAGGCTCGAGTGATCCTCCCACCACAGCCTCCCAAGTAGCTGGGACTACAGGCATGTA GACCTCCCAGGCTCGAGTGATCCTCCCACCACGGCCTCCCAAGTAGCTGGGACTACAGGCATGTA T C ZNF251 Ensembl:ENSG00000198169 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1323239609 Functional Loss SNV dbSNP153 33..33 33 - - - 10444 RMVar_ID_10444 Human_SNP_ID_386385855 A-to-I Human chr8 - 144750910 144750910 144750910 AGGAGGTAAAGGTTGCAGTGAGCCAAGATTGCACTACTGCACTCCAGCCTGAGTGACAGAGCGAG AGGAGGTAAAGGTTGCAGTGAGCCAAGATTGCGCTACTGCACTCCAGCCTGAGTGACAGAGCGAG T C ZNF251 Ensembl:ENSG00000198169 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1057486903 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10409951,Human_RBP_ID_26191239 10445 RMVar_ID_10445 Human_SNP_ID_386385856 A-to-I Human chr8 - 144750910 144750910 144750910 AGGAGGTAAAGGTTGCAGTGAGCCAAGATTGCACTACTGCACTCCAGCCTGAGTGACAGAGCGAG AGGAGGTAAAGGTTGCAGTGAGCCAAGATTGCCCTACTGCACTCCAGCCTGAGTGACAGAGCGAG T G ZNF251 Ensembl:ENSG00000198169 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1057486903 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10409951,Human_RBP_ID_26191239 10446 RMVar_ID_10446 Human_SNP_ID_386388152 A-to-I Human chr8 - 144758983 144758983 144758983 TAGAGATGGAGTTTCACCACGTTGGCCAGGCTAGTCTCAAACTCCTGACCTCAGTTGATCCGCTC TAGAGATGGAGTTTCACCACGTTGGCCAGGCTGGTCTCAAACTCCTGACCTCAGTTGATCCGCTC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs902498631 Functional Loss SNV dbSNP153 33..33 33 - - - 10447 RMVar_ID_10447 Human_SNP_ID_386394080 A-to-I Human chr8 - 144780961 144780961 144780961 CGGCTAATTTTTTTTGTATTTTCGGTAGAGACAGGGTTTCACCGTCAGCCAGGATGGTCTCGATC CGGCTAATTTTTTTTGTATTTTCGGTAGAGACGGGGTTTCACCGTCAGCCAGGATGGTCTCGATC T C ZNF34 Ensembl:ENSG00000196378 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1047321623 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7818432 10448 RMVar_ID_10448 Human_SNP_ID_386395705 A-to-I Human chr8 - 144786042 144786042 144786042 AGGCGGAGCTTGCAGTGAGCCAAGATCCCGCCACTGCTCTCCAGCCTGGGTGATGGAGCAAGACT AGGCGGAGCTTGCAGTGAGCCAAGATCCCGCCGCTGCTCTCCAGCCTGGGTGATGGAGCAAGACT T C ZNF34 Ensembl:ENSG00000196378 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs902828710 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21654475,Human_RBP_ID_26156982 10449 RMVar_ID_10449 Human_SNP_ID_386395712 A-to-I Human chr8 - 144786053 144786053 144786053 GTCAACTCGGGAGGCGGAGCTTGCAGTGAGCCAAGATCCCGCCACTGCTCTCCAGCCTGGGTGAT GTCAACTCGGGAGGCGGAGCTTGCAGTGAGCCGAGATCCCGCCACTGCTCTCCAGCCTGGGTGAT T C ZNF34 Ensembl:ENSG00000196378 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1401810025 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21654475 10450 RMVar_ID_10450 Human_SNP_ID_386395741 A-to-I Human chr8 - 144786157 144786157 144786157 CCAGTGAAACCCCGTCTCTACTAAAAAATACAAAAAAATTAGCCGGGCGTGGTAGCGGGCGCCTG CCAGTGAAACCCCGTCTCTACTAAAAAATACAGAAAAATTAGCCGGGCGTGGTAGCGGGCGCCTG T C ZNF34 Ensembl:ENSG00000196378 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs368619833 Functional Loss SNV dbSNP153 33..33 33 - - - 10451 RMVar_ID_10451 Human_SNP_ID_386395775 A-to-I Human chr8 - 144786261 144786261 144786261 TGTATGGCAGAGCACGGTGGCTCACGCCTGCAATCCCAGCACTTTGGGAGGCCAAGGCGCGGGGG TGTATGGCAGAGCACGGTGGCTCACGCCTGCAGTCCCAGCACTTTGGGAGGCCAAGGCGCGGGGG T C ZNF34 Ensembl:ENSG00000196378 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1404253277 Functional Loss SNV dbSNP153 33..33 33 - - - 10452 RMVar_ID_10452 Human_SNP_ID_386395832 A-to-I Human chr8 - 144786454 144786454 144786454 AATTTTTGTATTTTTAGTAGAGATGGGGTTTAACCATGTTGGCCAGGCTGGTCTCGAACTCCTGA AATTTTTGTATTTTTAGTAGAGATGGGGTTTATCCATGTTGGCCAGGCTGGTCTCGAACTCCTGA T A ZNF34 Ensembl:ENSG00000196378 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1365020867 Functional Loss SNV dbSNP153 33..33 33 - - - 10453 RMVar_ID_10453 Human_SNP_ID_386395833 A-to-I Human chr8 - 144786455 144786455 144786455 TAATTTTTGTATTTTTAGTAGAGATGGGGTTTAACCATGTTGGCCAGGCTGGTCTCGAACTCCTG TAATTTTTGTATTTTTAGTAGAGATGGGGTTTGACCATGTTGGCCAGGCTGGTCTCGAACTCCTG T C ZNF34 Ensembl:ENSG00000196378 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1021535474 Functional Loss SNV dbSNP153 33..33 33 - - - 10454 RMVar_ID_10454 Human_SNP_ID_386400754 A-to-I Human chr8 + 144801029 144801029 144801029 TTTTTGTATTTTTCGTAGAGAAGGGTTTCACCATGTTGGCCAGGCTGGTCACGAACTCCTGACTT TTTTTGTATTTTTCGTAGAGAAGGGTTTCACCGTGTTGGCCAGGCTGGTCACGAACTCCTGACTT A G ZNF517 Ensembl:ENSG00000197363 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs955191007 Functional Loss SNV dbSNP153 33..33 33 - - - 10455 RMVar_ID_10455 Human_SNP_ID_386403530 A-to-I Human chr8 + 144809246 144809246 144809246 GCAGGATCTCTCTGTCAGCCAGCCTGGAGTGCAATGGCACAATCATGGCTTACTGCAGCCTCCAG GCAGGATCTCTCTGTCAGCCAGCCTGGAGTGCGATGGCACAATCATGGCTTACTGCAGCCTCCAG A G ZNF517 Ensembl:ENSG00000197363 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs867510128 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1025396 10456 RMVar_ID_10456 Human_SNP_ID_386409996 A-to-I Human chr8 + 144832607 144832607 144832607 GACATTAGCCAGGCGTGGTGGCGGGTGGTTGTAATCTTGGCTTCTCAGGAGGCTGAGGCAGGAGA GACATTAGCCAGGCGTGGTGGCGGGTGGTTGTCATCTTGGCTTCTCAGGAGGCTGAGGCAGGAGA A C ZNF7 Ensembl:ENSG00000147789 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs969065282 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91295,RMVar_hsa_circ_82605,RMVar_hsa_circ_255192,RMVar_hsa_circ_303080,RMVar_hsa_circ_255193,RMVar_hsa_circ_98431,RMVar_hsa_circ_255195,RMVar_hsa_circ_255196 10457 RMVar_ID_10457 Human_SNP_ID_386409997 A-to-I Human chr8 + 144832607 144832607 144832607 GACATTAGCCAGGCGTGGTGGCGGGTGGTTGTAATCTTGGCTTCTCAGGAGGCTGAGGCAGGAGA GACATTAGCCAGGCGTGGTGGCGGGTGGTTGTGATCTTGGCTTCTCAGGAGGCTGAGGCAGGAGA A G ZNF7 Ensembl:ENSG00000147789 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs969065282 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91295,RMVar_hsa_circ_82605,RMVar_hsa_circ_255192,RMVar_hsa_circ_303080,RMVar_hsa_circ_255193,RMVar_hsa_circ_98431,RMVar_hsa_circ_255195,RMVar_hsa_circ_255196 10458 RMVar_ID_10458 Human_SNP_ID_386410260 A-to-I Human chr8 + 144833522 144833522 144833522 TCCTGAGTAGCTGGGATTACAGCTACTCAGGCATGTGCCACCACACCCGGCCAATTTTTTGTATT TCCTGAGTAGCTGGGATTACAGCTACTCAGGCGTGTGCCACCACACCCGGCCAATTTTTTGTATT A G ZNF7 Ensembl:ENSG00000147789 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs562227452 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91295,RMVar_hsa_circ_82605,RMVar_hsa_circ_255192,RMVar_hsa_circ_303080,RMVar_hsa_circ_255193,RMVar_hsa_circ_98431,RMVar_hsa_circ_255195,RMVar_hsa_circ_255196 10459 RMVar_ID_10459 Human_SNP_ID_386410380 A-to-I Human chr8 + 144833952 144833952 144833952 CAGGCATGTGCCACTACACCCGGCTAATTTTTATATTTTAAGTAGAGATGAGGTTTCACCATGTT CAGGCATGTGCCACTACACCCGGCTAATTTTTCTATTTTAAGTAGAGATGAGGTTTCACCATGTT A C ZNF7 Ensembl:ENSG00000147789 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1295242302 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91295,RMVar_hsa_circ_82605,RMVar_hsa_circ_255192,RMVar_hsa_circ_303080,RMVar_hsa_circ_255193,RMVar_hsa_circ_98431,RMVar_hsa_circ_255195,RMVar_hsa_circ_255196 10460 RMVar_ID_10460 Human_SNP_ID_386410381 A-to-I Human chr8 + 144833952 144833952 144833952 CAGGCATGTGCCACTACACCCGGCTAATTTTTATATTTTAAGTAGAGATGAGGTTTCACCATGTT CAGGCATGTGCCACTACACCCGGCTAATTTTTGTATTTTAAGTAGAGATGAGGTTTCACCATGTT A G ZNF7 Ensembl:ENSG00000147789 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1295242302 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91295,RMVar_hsa_circ_82605,RMVar_hsa_circ_255192,RMVar_hsa_circ_303080,RMVar_hsa_circ_255193,RMVar_hsa_circ_98431,RMVar_hsa_circ_255195,RMVar_hsa_circ_255196 10461 RMVar_ID_10461 Human_SNP_ID_386410382 A-to-I Human chr8 + 144833959 144833959 144833959 GTGCCACTACACCCGGCTAATTTTTATATTTTAAGTAGAGATGAGGTTTCACCATGTTGGCCAGG GTGCCACTACACCCGGCTAATTTTTATATTTTTAGTAGAGATGAGGTTTCACCATGTTGGCCAGG A T ZNF7 Ensembl:ENSG00000147789 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1563829126 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91295,RMVar_hsa_circ_82605,RMVar_hsa_circ_255192,RMVar_hsa_circ_303080,RMVar_hsa_circ_255193,RMVar_hsa_circ_98431,RMVar_hsa_circ_255195,RMVar_hsa_circ_255196 10462 RMVar_ID_10462 Human_SNP_ID_386414689 A-to-I Human chr8 - 144846759 144846759 144846759 AGGTGGCGGAGCTTGCAGTGAGCCGAGACCGCACCACTGCACTTCAGCCTGAGGGACAGAGCGAG AGGTGGCGGAGCTTGCAGTGAGCCGAGACCGCGCCACTGCACTTCAGCCTGAGGGACAGAGCGAG T C COMMD5 Ensembl:ENSG00000170619 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs922083390 Functional Loss SNV dbSNP153 33..33 33 - - - 10463 RMVar_ID_10463 Human_SNP_ID_386422282 A-to-I Human chr8 - 144877225 144877225 144877225 AAAATTAGCTGGGTGTTGTGGCTTGCGCCTGTAGTCCCAGATACGTGGGAGGCTAAGGTGGGAGG AAAATTAGCTGGGTGTTGTGGCTTGCGCCTGTGGTCCCAGATACGTGGGAGGCTAAGGTGGGAGG T C ZNF250 Ensembl:ENSG00000196150 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1132534 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77403,RMVar_hsa_circ_255197,RMVar_hsa_circ_114347,RMVar_hsa_circ_255198,RMVar_hsa_circ_255199,RMVar_hsa_circ_255200,RMVar_hsa_circ_255201 10464 RMVar_ID_10464 Human_SNP_ID_386424965 A-to-I Human chr8 - 144888434 144888433 144888434 TGCCCCTATACCCAGCTAATTTTTGTATTTTTAGTAGAGACAGGATTTCACCATGTTGGCCAGGC TGCCCCTATACCCAGCTAATTTTTGTATTTTT_GTAGAGACAGGATTTCACCATGTTGGCCAGGC CT C ZNF250 Ensembl:ENSG00000196150 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1230979059 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_77403,RMVar_hsa_circ_114347,RMVar_hsa_circ_51234,RMVar_hsa_circ_255199,RMVar_hsa_circ_255200,RMVar_hsa_circ_67182,RMVar_hsa_circ_255201,RMVar_hsa_circ_323646 10465 RMVar_ID_10465 Human_SNP_ID_386438355 A-to-I Human chr8 - 144940217 144940217 144940217 AAAATTAGCTGGGCGTGGTTGCTTGTGCTTGTAGTCCTAGTTACTTGGGAGGCTGAGATAGGAAG AAAATTAGCTGGGCGTGGTTGCTTGTGCTTGTTGTCCTAGTTACTTGGGAGGCTGAGATAGGAAG T A ZNF16 Ensembl:ENSG00000170631 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1281073941 Functional Loss SNV dbSNP153 33..33 33 - - - 10466 RMVar_ID_10466 Human_SNP_ID_386448101 A-to-I Human chr8 - 144974308 144974308 144974308 AACTCCTGGGCTCAAGTGATTCCCCTGCCTCAACTTCATGAGTAGCAGGGACTACAGCTGTGTAC AACTCCTGGGCTCAAGTGATTCCCCTGCCTCAGCTTCATGAGTAGCAGGGACTACAGCTGTGTAC T C ZNF252P Ensembl:ENSG00000196922 Pseudogene exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs527476698 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17547369 RMVar_hsa_circ_105791,RMVar_hsa_circ_255207,RMVar_hsa_circ_100817,RMVar_hsa_circ_255206 10467 RMVar_ID_10467 Human_SNP_ID_386448112 A-to-I Human chr8 - 144974357 144974357 144974357 TTGCACAGGGTGGAGTGCAGTGGTGCAGTCATAGCTCACTGTAACCTTGAACTCCTGGGCTCAAG TTGCACAGGGTGGAGTGCAGTGGTGCAGTCATGGCTCACTGTAACCTTGAACTCCTGGGCTCAAG T C ZNF252P Ensembl:ENSG00000196922 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs11541176 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10408446 RMVar_hsa_circ_105791,RMVar_hsa_circ_255207,RMVar_hsa_circ_100817,RMVar_hsa_circ_255206 10468 RMVar_ID_10468 Human_SNP_ID_386454093 A-to-I Human chr8 - 144995089 144995089 144995089 GAATCTGTGATCTTGAGGTGGCTGCACAGGCCACCAGTGCCCCCAGACTGGTCAGAGATCTCGTA GAATCTGTGATCTTGAGGTGGCTGCACAGGCCGCCAGTGCCCCCAGACTGGTCAGAGATCTCGTA T C ZNF252P Ensembl:ENSG00000196922 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs773043014 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19143145 RMVar_hsa_circ_105791,RMVar_hsa_circ_255207 10469 RMVar_ID_10469 Human_SNP_ID_386454094 A-to-I Human chr8 - 144995089 144995089 144995089 GAATCTGTGATCTTGAGGTGGCTGCACAGGCCACCAGTGCCCCCAGACTGGTCAGAGATCTCGTA GAATCTGTGATCTTGAGGTGGCTGCACAGGCCCCCAGTGCCCCCAGACTGGTCAGAGATCTCGTA T G ZNF252P Ensembl:ENSG00000196922 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs773043014 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19143145 RMVar_hsa_circ_105791,RMVar_hsa_circ_255207 10470 RMVar_ID_10470 Human_SNP_ID_386454097 A-to-I Human chr8 - 144995096 144995096 144995096 GCCAGCAGAATCTGTGATCTTGAGGTGGCTGCACAGGCCACCAGTGCCCCCAGACTGGTCAGAGA GCCAGCAGAATCTGTGATCTTGAGGTGGCTGCGCAGGCCACCAGTGCCCCCAGACTGGTCAGAGA T C ZNF252P Ensembl:ENSG00000196922 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1422466086 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19143145 RMVar_hsa_circ_105791,RMVar_hsa_circ_255207 10471 RMVar_ID_10471 Human_SNP_ID_386454115 A-to-I Human chr8 - 144995135 144995135 144995135 TTTCCCCTTGGTTGTATTCTTTTTGGAGTAGAAAATATGGCCAGCAGAATCTGTGATCTTGAGGT TTTCCCCTTGGTTGTATTCTTTTTGGAGTAGAGAATATGGCCAGCAGAATCTGTGATCTTGAGGT T C ZNF252P Ensembl:ENSG00000196922 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1239849078 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105791,RMVar_hsa_circ_255207 10472 RMVar_ID_10472 Human_SNP_ID_386454156 A-to-I Human chr8 + 144995232 144995232 144995232 TGAAGTGTGTTTTGAGAGCAAGGAAACAGGGCAGATACCTGACCAACTTGTGATCCTAGACATGA TGAAGTGTGTTTTGAGAGCAAGGAAACAGGGCGGATACCTGACCAACTTGTGATCCTAGACATGA A G TMED10P1 Ensembl:ENSG00000254618 Pseudogene exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs878987687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21655965,Human_RBP_ID_22409766,Human_RBP_ID_26554106 Human_miRNA_ID_1886397,Human_miRNA_ID_1910063 10473 RMVar_ID_10473 Human_SNP_ID_386454180 A-to-I Human chr8 + 144995291 144995290 144995292 ACATGAAGCATGGAGTGGAGGTGAAAAATTACAGAGAGATTGCAAAAGTTGAGAAGCTCAAACCA ACATGAAGCATGGAGTGGAGGTGAAAAATTAC__AGAGATTGCAAAAGTTGAGAAGCTCAAACCA CAG C TMED10P1 Ensembl:ENSG00000254618 Pseudogene exon GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs753014992 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_21655965,Human_RBP_ID_22409767 Human_miRNA_ID_1842465,Human_miRNA_ID_1875970 10474 RMVar_ID_10474 Human_SNP_ID_386454182 A-to-I Human chr8 + 144995291 144995291 144995291 ACATGAAGCATGGAGTGGAGGTGAAAAATTACAGAGAGATTGCAAAAGTTGAGAAGCTCAAACCA ACATGAAGCATGGAGTGGAGGTGAAAAATTACGGAGAGATTGCAAAAGTTGAGAAGCTCAAACCA A G TMED10P1 Ensembl:ENSG00000254618 Pseudogene exon GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs879235930 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21655965,Human_RBP_ID_22409767 Human_miRNA_ID_1842465,Human_miRNA_ID_1875970 10475 RMVar_ID_10475 Human_SNP_ID_386470770 A-to-I Human chr8 + 145055764 145055764 145055764 TTAGATAGCAGGAGCAAATTAGTGAAAGTACTAAATGTCTGATATGCAGAAATAATGGCATAAGC TTAGATAGCAGGAGCAAATTAGTGAAAGTACTTAATGTCTGATATGCAGAAATAATGGCATAAGC A T C8orf33 Ensembl:ENSG00000182307 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1563955820 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_696276,Human_RBP_ID_18388251,Human_RBP_ID_21599529,Human_RBP_ID_24250654 Human_miRNA_ID_585116,Human_miRNA_ID_2471055,Human_miRNA_ID_2632828 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 10476 RMVar_ID_10476 Human_SNP_ID_386470780 A-to-I Human chr8 + 145055791 145055791 145055791 GTACTAAATGTCTGATATGCAGAAATAATGGCATAAGCTGTCTCTCTCTCTTCTCTCTCTCTCTG GTACTAAATGTCTGATATGCAGAAATAATGGCGTAAGCTGTCTCTCTCTCTTCTCTCTCTCTCTG A G C8orf33 Ensembl:ENSG00000182307 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs539518858 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_696276,Human_RBP_ID_4998926,Human_RBP_ID_8683524,Human_RBP_ID_24250655 Human_miRNA_ID_576781,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 10477 RMVar_ID_10477 Human_SNP_ID_386470841 A-to-I Human chr8 + 145055932 145055932 145055932 GGTTCACATTCCTTACCCTGCCCCTTTGTCTTATATCCAATAAATATCAGTGCAGCCTGGCATTT GGTTCACATTCCTTACCCTGCCCCTTTGTCTTGTATCCAATAAATATCAGTGCAGCCTGGCATTT A G C8orf33 Ensembl:ENSG00000182307 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1134051 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_696279 Human_miRNA_ID_557050,Human_miRNA_ID_559475,Human_miRNA_ID_1216149,Human_miRNA_ID_1468124,Human_miRNA_ID_2364065 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 10478 RMVar_ID_10478 Human_SNP_ID_337625945 A-to-I Human chr7 + 120298911 120298911 120298911 CTGGCGCGGTGGCTCACACCTTTAATCCCAGCACTTTGGAAGGCCGAGGTGGGTGGATCACCTGA CTGGCGCGGTGGCTCACACCTTTAATCCCAGCGCTTTGGAAGGCCGAGGTGGGTGGATCACCTGA A G KCND2 Ensembl:ENSG00000184408 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1404934619 Functional Loss SNV dbSNP153 33..33 33 - - - 10479 RMVar_ID_10479 Human_SNP_ID_337670081 A-to-I Human chr7 + 120487903 120487903 120487903 AAAACCAAATTCAAAATTAGTTATGTACAGCCAGGTGTGGTGACTCATGCCTGTAACCCTAGCAC AAAACCAAATTCAAAATTAGTTATGTACAGCCGGGTGTGGTGACTCATGCCTGTAACCCTAGCAC A G KCND2 Ensembl:ENSG00000184408 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1016966930 Functional Loss SNV dbSNP153 33..33 33 - - - 10480 RMVar_ID_10480 Human_SNP_ID_337738851 A-to-I Human chr7 - 120788421 120788421 120788421 TTTAAAATGAGGATGGAAAAGTTTCATGTCATAAGTCACCACCTGGACAATAATTGATGCCCTTA TTTAAAATGAGGATGGAAAAGTTTCATGTCATGAGTCACCACCTGGACAATAATTGATGCCCTTA T C TSPAN12 Ensembl:ENSG00000106025 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs925396692 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8907190,Human_RBP_ID_17311269,Human_RBP_ID_17423794,Human_RBP_ID_17539084,Human_RBP_ID_18377427,Human_RBP_ID_27762898 Human_miRNA_ID_861689 10481 RMVar_ID_10481 Human_SNP_ID_337776690 A-to-I Human chr7 + 120954315 120954315 120954315 GGGCGTGGTGGTGGGCGCCTGTGATCCCAGCTACTCGAGAGACTGAGACAGGAGAATCACTTGAA GGGCGTGGTGGTGGGCGCCTGTGATCCCAGCTGCTCGAGAGACTGAGACAGGAGAATCACTTGAA A G ING3 Ensembl:ENSG00000071243 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs919074871 Functional Loss SNV dbSNP153 33..33 33 - - - 10482 RMVar_ID_10482 Human_SNP_ID_337776691 A-to-I Human chr7 + 120954315 120954315 120954315 GGGCGTGGTGGTGGGCGCCTGTGATCCCAGCTACTCGAGAGACTGAGACAGGAGAATCACTTGAA GGGCGTGGTGGTGGGCGCCTGTGATCCCAGCTTCTCGAGAGACTGAGACAGGAGAATCACTTGAA A T ING3 Ensembl:ENSG00000071243 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs919074871 Functional Loss SNV dbSNP153 33..33 33 - - - 10483 RMVar_ID_10483 Human_SNP_ID_337873609 A-to-I Human chr7 - 121360648 121360648 121360648 TAAATTTTTTTGTTGAGATGAGGTCTCACTATATTGCCCAGGCTGGTTTCAAGCTCCTGGGCTCA TAAATTTTTTTGTTGAGATGAGGTCTCACTATGTTGCCCAGGCTGGTTTCAAGCTCCTGGGCTCA T C FAM3C Ensembl:ENSG00000196937 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1183008002 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67874,RMVar_hsa_circ_248043,RMVar_hsa_circ_334366,RMVar_hsa_circ_371398,RMVar_hsa_circ_248044 10484 RMVar_ID_10484 Human_SNP_ID_337873610 A-to-I Human chr7 - 121360650 121360650 121360650 TTTAAATTTTTTTGTTGAGATGAGGTCTCACTATATTGCCCAGGCTGGTTTCAAGCTCCTGGGCT TTTAAATTTTTTTGTTGAGATGAGGTCTCACTGTATTGCCCAGGCTGGTTTCAAGCTCCTGGGCT T C FAM3C Ensembl:ENSG00000196937 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs994082249 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67874,RMVar_hsa_circ_248043,RMVar_hsa_circ_334366,RMVar_hsa_circ_371398,RMVar_hsa_circ_248044 10485 RMVar_ID_10485 Human_SNP_ID_337873626 A-to-I Human chr7 - 121360706 121360706 121360706 CCTCAACTTCCTGAGTAGCTAGGACTACAGGCATGTGCCACCAAGCTCGGCTAATTTTTAAATTT CCTCAACTTCCTGAGTAGCTAGGACTACAGGCTTGTGCCACCAAGCTCGGCTAATTTTTAAATTT T A FAM3C Ensembl:ENSG00000196937 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1325714293 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67874,RMVar_hsa_circ_248043,RMVar_hsa_circ_334366,RMVar_hsa_circ_371398,RMVar_hsa_circ_248044 10486 RMVar_ID_10486 Human_SNP_ID_337873627 A-to-I Human chr7 - 121360706 121360706 121360706 CCTCAACTTCCTGAGTAGCTAGGACTACAGGCATGTGCCACCAAGCTCGGCTAATTTTTAAATTT CCTCAACTTCCTGAGTAGCTAGGACTACAGGCGTGTGCCACCAAGCTCGGCTAATTTTTAAATTT T C FAM3C Ensembl:ENSG00000196937 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1325714293 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67874,RMVar_hsa_circ_248043,RMVar_hsa_circ_334366,RMVar_hsa_circ_371398,RMVar_hsa_circ_248044 10487 RMVar_ID_10487 Human_SNP_ID_337875501 A-to-I Human chr7 - 121369118 121369118 121369118 AGTTAGCCGGGCGTGGTGGCACATGGGCCTGTAATCCTAGCTACTTGGGAGGCTGAGGCACGAGA AGTTAGCCGGGCGTGGTGGCACATGGGCCTGTGATCCTAGCTACTTGGGAGGCTGAGGCACGAGA T C FAM3C Ensembl:ENSG00000196937 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs537448114 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67874,RMVar_hsa_circ_248043,RMVar_hsa_circ_334366,RMVar_hsa_circ_371398,RMVar_hsa_circ_248044 10488 RMVar_ID_10488 Human_SNP_ID_338113358 A-to-I Human chr7 - 122338889 122338889 122338889 TAGCATGATAGTATGTTCCTGTAGTCCTAGCTACTTCGGAGGCTAAGGCGAGAGGATCATCCAAG TAGCATGATAGTATGTTCCTGTAGTCCTAGCTGCTTCGGAGGCTAAGGCGAGAGGATCATCCAAG T C CADPS2 Ensembl:ENSG00000081803 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs901768273 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_248095 10489 RMVar_ID_10489 Human_SNP_ID_338133974 A-to-I Human chr7 - 122425383 122425383 122425383 GGGTTTCGCCACGTTGCCCAGGCTGGTCTTGAACTCCTGAACCCAAGCAATCCACCCACCTCAGC GGGTTTCGCCACGTTGCCCAGGCTGGTCTTGAGCTCCTGAACCCAAGCAATCCACCCACCTCAGC T C CADPS2 Ensembl:ENSG00000081803 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs897008480 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60194,RMVar_hsa_circ_284158,RMVar_hsa_circ_43995,RMVar_hsa_circ_79652,RMVar_hsa_circ_316416,RMVar_hsa_circ_365411,RMVar_hsa_circ_337584,RMVar_hsa_circ_113116,RMVar_hsa_circ_248108,RMVar_hsa_circ_71568,RMVar_hsa_circ_248109,RMVar_hsa_circ_248107,RMVar_hsa_circ_74614,RMVar_hsa_circ_324575,RMVar_hsa_circ_268847,RMVar_hsa_circ_63970,RMVar_hsa_circ_248111,RMVar_hsa_circ_66619,RMVar_hsa_circ_53774,RMVar_hsa_circ_248112 10490 RMVar_ID_10490 Human_SNP_ID_338147349 A-to-I Human chr7 - 122481242 122481242 122481242 CTGCTGACGTGAACCTGGGAGGCAGAGCTTGCAGTGAGCCACGTTCGCACCACTGCACTCCAGCC CTGCTGACGTGAACCTGGGAGGCAGAGCTTGCGGTGAGCCACGTTCGCACCACTGCACTCCAGCC T C CADPS2 Ensembl:ENSG00000081803 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs902063730 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60194,RMVar_hsa_circ_43995,RMVar_hsa_circ_337584,RMVar_hsa_circ_71568,RMVar_hsa_circ_74614,RMVar_hsa_circ_268847,RMVar_hsa_circ_53774,RMVar_hsa_circ_54830,RMVar_hsa_circ_57462,RMVar_hsa_circ_72606,RMVar_hsa_circ_70289,RMVar_hsa_circ_248115,RMVar_hsa_circ_299207,RMVar_hsa_circ_358225,RMVar_hsa_circ_364189,RMVar_hsa_circ_335621,RMVar_hsa_circ_54772,RMVar_hsa_circ_96454 10491 RMVar_ID_10491 Human_SNP_ID_338152136 A-to-I Human chr7 - 122501020 122501020 122501020 GAACTCCTAGCCTCAAGTGATCATCTCACCTCAGCCTCCCAAAGTGCTGGGATTCCAGGTACAAG GAACTCCTAGCCTCAAGTGATCATCTCACCTCGGCCTCCCAAAGTGCTGGGATTCCAGGTACAAG T C CADPS2 Ensembl:ENSG00000081803 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs942026775 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60194,RMVar_hsa_circ_43995,RMVar_hsa_circ_337584,RMVar_hsa_circ_71568,RMVar_hsa_circ_74614,RMVar_hsa_circ_268847,RMVar_hsa_circ_54830,RMVar_hsa_circ_57462,RMVar_hsa_circ_72606,RMVar_hsa_circ_248115,RMVar_hsa_circ_299207,RMVar_hsa_circ_358225,RMVar_hsa_circ_335621,RMVar_hsa_circ_54772,RMVar_hsa_circ_96454,RMVar_hsa_circ_268884,RMVar_hsa_circ_358903,RMVar_hsa_circ_248116 10492 RMVar_ID_10492 Human_SNP_ID_338152775 A-to-I Human chr7 - 122503313 122503313 122503313 GAAAATTGTATTGGCCGTGCACAGTGGCTCACACCTGTAATCCCAGCATTTTGGGAGGCCGAGGC GAAAATTGTATTGGCCGTGCACAGTGGCTCACGCCTGTAATCCCAGCATTTTGGGAGGCCGAGGC T C CADPS2 Ensembl:ENSG00000081803 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs753429861 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60194,RMVar_hsa_circ_43995,RMVar_hsa_circ_337584,RMVar_hsa_circ_71568,RMVar_hsa_circ_74614,RMVar_hsa_circ_268847,RMVar_hsa_circ_54830,RMVar_hsa_circ_57462,RMVar_hsa_circ_72606,RMVar_hsa_circ_248115,RMVar_hsa_circ_299207,RMVar_hsa_circ_358225,RMVar_hsa_circ_335621,RMVar_hsa_circ_54772,RMVar_hsa_circ_96454,RMVar_hsa_circ_268884,RMVar_hsa_circ_358903,RMVar_hsa_circ_248116 10493 RMVar_ID_10493 Human_SNP_ID_338164237 A-to-I Human chr7 - 122549443 122549443 122549443 CTAAATTTTGTATTAATTAGGCTAATTATACAATCACACGAATGTCTTGAGTGCGATGGTAACTA CTAAATTTTGTATTAATTAGGCTAATTATACAGTCACACGAATGTCTTGAGTGCGATGGTAACTA T C CADPS2 Ensembl:ENSG00000081803 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs575781038 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17046285 RMVar_hsa_circ_43995,RMVar_hsa_circ_71568,RMVar_hsa_circ_74614,RMVar_hsa_circ_268847,RMVar_hsa_circ_54830,RMVar_hsa_circ_72606,RMVar_hsa_circ_248115,RMVar_hsa_circ_358225,RMVar_hsa_circ_335621,RMVar_hsa_circ_54772,RMVar_hsa_circ_96454,RMVar_hsa_circ_63916,RMVar_hsa_circ_268884,RMVar_hsa_circ_358903,RMVar_hsa_circ_248116,RMVar_hsa_circ_366345 10494 RMVar_ID_10494 Human_SNP_ID_338225689 A-to-I Human chr7 - 122782483 122782483 122782483 CCTTAGCATCCTGAGTAGCTGGGACCGCAGACATGCATCACTACACCGTGCTAATTTTTGTTGTT CCTTAGCATCCTGAGTAGCTGGGACCGCAGACGTGCATCACTACACCGTGCTAATTTTTGTTGTT T C CADPS2 Ensembl:ENSG00000081803 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs952760315 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_248122,RMVar_hsa_circ_122522 10495 RMVar_ID_10495 Human_SNP_ID_338408771 A-to-I Human chr7 - 123541255 123541255 123541255 TCAGGATAGAGGTAGAGTTTCTGTAAAAGAAGAGACATTAAGAGTTCCTGAAATTTATATCTGGC TCAGGATAGAGGTAGAGTTTCTGTAAAAGAAGGGACATTAAGAGTTCCTGAAATTTATATCTGGC T C NDUFA5 Ensembl:ENSG00000128609 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs904658275 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_3087994 RMVar_hsa_circ_77541,RMVar_hsa_circ_101321,RMVar_hsa_circ_120573,RMVar_hsa_circ_248127,RMVar_hsa_circ_248128,RMVar_hsa_circ_248129 10496 RMVar_ID_10496 Human_SNP_ID_338844223 A-to-I Human chr7 + 125345142 125345139 125345142 ATGGCGTAAGAAAACTCTGGACCAGGTCTTAGAAGATATAGACCAGTGCTGTCAAGCTCTCTCTA ATGGCGTAAGAAAACTCTGGACCAGGTCTT___AGATATAGACCAGTGCTGTCAAGCTCTCTCTA TAGA T POT1-AS1,AC010099.2 Ensembl:ENSG00000224897,Ensembl:ENSG00000234071 lincRNA,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1157032878 Functional Loss DEL dbSNP153 31..33 33 - - - RMVar_hsa_circ_11414,RMVar_hsa_circ_248154,RMVar_hsa_circ_311502 10497 RMVar_ID_10497 Human_SNP_ID_339410187 A-to-I Human chr7 + 127687950 127687950 127687950 ATTCAAGCAATCTTTCTGCCTCGCCCTAAAGTACTGGGATTACAGGTGTGAGCCACTGCCCCTGG ATTCAAGCAATCTTTCTGCCTCGCCCTAAAGTGCTGGGATTACAGGTGTGAGCCACTGCCCCTGG A G SND1 Ensembl:ENSG00000197157 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs898829684 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29121,RMVar_hsa_circ_99457,RMVar_hsa_circ_357619,RMVar_hsa_circ_362402,RMVar_hsa_circ_248176,RMVar_hsa_circ_374183,RMVar_hsa_circ_361312,RMVar_hsa_circ_109575,RMVar_hsa_circ_329361,RMVar_hsa_circ_44175,RMVar_hsa_circ_248178,RMVar_hsa_circ_248180,RMVar_hsa_circ_28567,RMVar_hsa_circ_248179,RMVar_hsa_circ_248177 10498 RMVar_ID_10498 Human_SNP_ID_339411006 A-to-I Human chr7 + 127691668 127691668 127691668 GGAGCCTCGCTTTGTCGCCCGGGCTGGAGTGCAGTGGCGCAATCTTGGCTCACTGCAACCTCCAC GGAGCCTCGCTTTGTCGCCCGGGCTGGAGTGCGGTGGCGCAATCTTGGCTCACTGCAACCTCCAC A G SND1 Ensembl:ENSG00000197157 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1387552377 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29121,RMVar_hsa_circ_99457,RMVar_hsa_circ_357619,RMVar_hsa_circ_362402,RMVar_hsa_circ_248176,RMVar_hsa_circ_374183,RMVar_hsa_circ_361312,RMVar_hsa_circ_109575,RMVar_hsa_circ_329361,RMVar_hsa_circ_44175,RMVar_hsa_circ_248178,RMVar_hsa_circ_248180,RMVar_hsa_circ_28567,RMVar_hsa_circ_248179,RMVar_hsa_circ_248177 10499 RMVar_ID_10499 Human_SNP_ID_339411013 A-to-I Human chr7 + 127691699 127691699 127691699 CAGTGGCGCAATCTTGGCTCACTGCAACCTCCACCTCACAGGTTCAAGCAATTCTCCTGTCTCAG CAGTGGCGCAATCTTGGCTCACTGCAACCTCCCCCTCACAGGTTCAAGCAATTCTCCTGTCTCAG A C SND1 Ensembl:ENSG00000197157 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1013240618 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29121,RMVar_hsa_circ_99457,RMVar_hsa_circ_357619,RMVar_hsa_circ_362402,RMVar_hsa_circ_248176,RMVar_hsa_circ_374183,RMVar_hsa_circ_361312,RMVar_hsa_circ_109575,RMVar_hsa_circ_329361,RMVar_hsa_circ_44175,RMVar_hsa_circ_248178,RMVar_hsa_circ_248180,RMVar_hsa_circ_28567,RMVar_hsa_circ_248179,RMVar_hsa_circ_248177 10500 RMVar_ID_10500 Human_SNP_ID_339411014 A-to-I Human chr7 + 127691699 127691699 127691699 CAGTGGCGCAATCTTGGCTCACTGCAACCTCCACCTCACAGGTTCAAGCAATTCTCCTGTCTCAG CAGTGGCGCAATCTTGGCTCACTGCAACCTCCTCCTCACAGGTTCAAGCAATTCTCCTGTCTCAG A T SND1 Ensembl:ENSG00000197157 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1013240618 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29121,RMVar_hsa_circ_99457,RMVar_hsa_circ_357619,RMVar_hsa_circ_362402,RMVar_hsa_circ_248176,RMVar_hsa_circ_374183,RMVar_hsa_circ_361312,RMVar_hsa_circ_109575,RMVar_hsa_circ_329361,RMVar_hsa_circ_44175,RMVar_hsa_circ_248178,RMVar_hsa_circ_248180,RMVar_hsa_circ_28567,RMVar_hsa_circ_248179,RMVar_hsa_circ_248177 10501 RMVar_ID_10501 Human_SNP_ID_339421347 A-to-I Human chr7 + 127737530 127737530 127737530 CTGGGAGGCAGAGGTTGCAGGGAGCCGAGATCACAACATTGCACTCCAGCCTGGGCGATAAGAAT CTGGGAGGCAGAGGTTGCAGGGAGCCGAGATCGCAACATTGCACTCCAGCCTGGGCGATAAGAAT A G SND1 Ensembl:ENSG00000197157 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1394389664 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15995841,Human_RBP_ID_22731231,Human_RBP_ID_26068366 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 10502 RMVar_ID_10502 Human_SNP_ID_339479512 A-to-I Human chr7 - 128000446 128000446 128000446 GGAGGGTCACCTGAGCCTGGGAGGTTGAGGCTACAGTGAGCCATGACTGTGCCACTGCATTCCAG GGAGGGTCACCTGAGCCTGGGAGGTTGAGGCTGCAGTGAGCCATGACTGTGCCACTGCATTCCAG T C - - Other Unknown GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1337170523 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_248202 10503 RMVar_ID_10503 Human_SNP_ID_339489988 A-to-I Human chr7 + 128042734 128042734 128042734 AAGAATTCTGCTCCTGAACATCTGGTAGCTGCAAGGTAAAATTCTTTACCAAATTGAGACCAAGA AAGAATTCTGCTCCTGAACATCTGGTAGCTGCTAGGTAAAATTCTTTACCAAATTGAGACCAAGA A T SND1 Ensembl:ENSG00000197157 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1484018262 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1862,RMVar_hsa_circ_56878 10504 RMVar_ID_10504 Human_SNP_ID_339500300 A-to-I Human chr7 + 128088176 128088176 128088176 GTCGGTGAAGACAGACATGTGGAGTCAGGTGCAGTGGCTCACGCCTGTAATCCCAGCATAGGAGG GTCGGTGAAGACAGACATGTGGAGTCAGGTGCCGTGGCTCACGCCTGTAATCCCAGCATAGGAGG A C SND1 Ensembl:ENSG00000197157 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs936880742 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76934,RMVar_hsa_circ_110969,RMVar_hsa_circ_248203,RMVar_hsa_circ_248206,RMVar_hsa_circ_86874,RMVar_hsa_circ_248205,RMVar_hsa_circ_81641,RMVar_hsa_circ_37347,RMVar_hsa_circ_248208 10505 RMVar_ID_10505 Human_SNP_ID_339500301 A-to-I Human chr7 + 128088176 128088176 128088176 GTCGGTGAAGACAGACATGTGGAGTCAGGTGCAGTGGCTCACGCCTGTAATCCCAGCATAGGAGG GTCGGTGAAGACAGACATGTGGAGTCAGGTGCGGTGGCTCACGCCTGTAATCCCAGCATAGGAGG A G SND1 Ensembl:ENSG00000197157 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs936880742 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76934,RMVar_hsa_circ_110969,RMVar_hsa_circ_248203,RMVar_hsa_circ_248206,RMVar_hsa_circ_86874,RMVar_hsa_circ_248205,RMVar_hsa_circ_81641,RMVar_hsa_circ_37347,RMVar_hsa_circ_248208 10506 RMVar_ID_10506 Human_SNP_ID_339500433 A-to-I Human chr7 + 128088552 128088547 128088552 TCGGCTCACTGCAACCTCTCCCTCCCAGGTTGAAGTGATTCTCCCACCTCAGCCTTCCGAGTAGC TCGGCTCACTGCAACCTCTCCCTCCCAG_____AGTGATTCTCCCACCTCAGCCTTCCGAGTAGC GGTTGA G SND1 Ensembl:ENSG00000197157 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1209790238 Functional Loss DEL dbSNP153 29..33 33 - - - RMVar_hsa_circ_76934,RMVar_hsa_circ_110969,RMVar_hsa_circ_248203,RMVar_hsa_circ_248206,RMVar_hsa_circ_86874,RMVar_hsa_circ_248205,RMVar_hsa_circ_81641,RMVar_hsa_circ_37347,RMVar_hsa_circ_248208 10507 RMVar_ID_10507 Human_SNP_ID_339500438 A-to-I Human chr7 + 128088552 128088552 128088552 TCGGCTCACTGCAACCTCTCCCTCCCAGGTTGAAGTGATTCTCCCACCTCAGCCTTCCGAGTAGC TCGGCTCACTGCAACCTCTCCCTCCCAGGTTGCAGTGATTCTCCCACCTCAGCCTTCCGAGTAGC A C SND1 Ensembl:ENSG00000197157 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs763296051 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76934,RMVar_hsa_circ_110969,RMVar_hsa_circ_248203,RMVar_hsa_circ_248206,RMVar_hsa_circ_86874,RMVar_hsa_circ_248205,RMVar_hsa_circ_81641,RMVar_hsa_circ_37347,RMVar_hsa_circ_248208 10508 RMVar_ID_10508 Human_SNP_ID_339552429 A-to-I Human chr7 - 128305522 128305522 128305522 GCCCAGGAGTTCAGGACTAGCCTGGGCAACATAGCAAGATCCCACCTCTACAAAAAAAGAAAAAA GCCCAGGAGTTCAGGACTAGCCTGGGCAACATGGCAAGATCCCACCTCTACAAAAAAAGAAAAAA T C RBM28 Ensembl:ENSG00000106344 Protein coding 3'UTR GSE100210;GSE99789 HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 29129909,29796672 RNA-Seq:(High) rs1296247319 Functional Loss SNV dbSNP153 33..33 33 - - - 10509 RMVar_ID_10509 Human_SNP_ID_339552445 A-to-I Human chr7 - 128305598 128305598 128305598 CTTCCCTCGGCTTGGCATGGTGGCTCATGCCTATATTCCCAGCACTTTGAGAGGTCAAAGTGGGA CTTCCCTCGGCTTGGCATGGTGGCTCATGCCTGTATTCCCAGCACTTTGAGAGGTCAAAGTGGGA T C RBM28 Ensembl:ENSG00000106344 Protein coding 3'UTR GSE100210;GSE99789 HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 29129909,29796672 RNA-Seq:(High) rs948372508 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21425400,Human_RBP_ID_26542934 10510 RMVar_ID_10510 Human_SNP_ID_339552927 A-to-I Human chr7 - 128307922 128307922 128307922 AAACAACAGGTGGGGCACAGAGTCTCATACCTATGATTGCAGCACTTCGGGAGGTGGGAGGATTG AAACAACAGGTGGGGCACAGAGTCTCATACCTGTGATTGCAGCACTTCGGGAGGTGGGAGGATTG T C RBM28 Ensembl:ENSG00000106344 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs1165298322 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7691038,Human_RBP_ID_16000557,Human_RBP_ID_23248936 10511 RMVar_ID_10511 Human_SNP_ID_339590364 A-to-I Human chr7 + 128457741 128457741 128457741 CGAGACCAGCCTCGCCAACATGGCGAAACCCCATCTCTACTAAAAATACAAAAGTTAGCTGGGTG CGAGACCAGCCTCGCCAACATGGCGAAACCCCGTCTCTACTAAAAATACAAAAGTTAGCTGGGTG A G AC010655.2,AC010655.4,HILPDA Ensembl:ENSG00000240758,Ensembl:ENSG00000273184,Ensembl:ENSG00000135245 lincRNA,lincRNA,Protein coding intron,intron,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs3178944 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_173380 RMVar_hsa_circ_77599,RMVar_hsa_circ_110104,RMVar_hsa_circ_248220,RMVar_hsa_circ_248221 10512 RMVar_ID_10512 Human_SNP_ID_339590928 A-to-I Human chr7 + 128460270 128460270 128460270 CATTTAGAAAACTGCAAGTTCAGGCCAGGTGCAGTGCCTCACGCCTGTAATCCCAGCACTTTGGG CATTTAGAAAACTGCAAGTTCAGGCCAGGTGCCGTGCCTCACGCCTGTAATCCCAGCACTTTGGG A C AC010655.2,AC010655.4 Ensembl:ENSG00000240758,Ensembl:ENSG00000273184 lincRNA,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs983520223 Functional Loss SNV dbSNP153 33..33 33 - - - 10513 RMVar_ID_10513 Human_SNP_ID_339591096 A-to-I Human chr7 + 128460817 128460815 128460817 CACCTCCCGGGCTCAAGCAATTCTCCTGTCTCAGCCTCCCCAGTAACTGGGACTACAGGTGCACA CACCTCCCGGGCTCAAGCAATTCTCCTGTCT__GCCTCCCCAGTAACTGGGACTACAGGTGCACA TCA T AC010655.2,AC010655.4 Ensembl:ENSG00000240758,Ensembl:ENSG00000273184 lincRNA,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1174495077 Functional Loss DEL dbSNP153 32..33 33 - - - 10514 RMVar_ID_10514 Human_SNP_ID_339591097 A-to-I Human chr7 + 128460817 128460817 128460817 CACCTCCCGGGCTCAAGCAATTCTCCTGTCTCAGCCTCCCCAGTAACTGGGACTACAGGTGCACA CACCTCCCGGGCTCAAGCAATTCTCCTGTCTCTGCCTCCCCAGTAACTGGGACTACAGGTGCACA A T AC010655.2,AC010655.4 Ensembl:ENSG00000240758,Ensembl:ENSG00000273184 lincRNA,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1464754897 Functional Loss SNV dbSNP153 33..33 33 - - - 10515 RMVar_ID_10515 Human_SNP_ID_339591124 A-to-I Human chr7 + 128460935 128460935 128460935 TTGCCCAGACTGTCCTCGAACCCCTTGGACTCAAGTGATCCACCCGTCTCAGCCTTCCAAAGTGC TTGCCCAGACTGTCCTCGAACCCCTTGGACTCCAGTGATCCACCCGTCTCAGCCTTCCAAAGTGC A C AC010655.2,AC010655.4 Ensembl:ENSG00000240758,Ensembl:ENSG00000273184 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs976078281 Functional Loss SNV dbSNP153 33..33 33 - - - 10516 RMVar_ID_10516 Human_SNP_ID_339591139 A-to-I Human chr7 + 128460975 128460975 128460975 CACCCGTCTCAGCCTTCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCACCCGGCCCACTACT CACCCGTCTCAGCCTTCCAAAGTGCTGGGATTGCAGGTGTGAGCCACCGCACCCGGCCCACTACT A G AC010655.2,AC010655.4 Ensembl:ENSG00000240758,Ensembl:ENSG00000273184 lincRNA,lincRNA intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1355176778 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26069064 10517 RMVar_ID_10517 Human_SNP_ID_339591172 A-to-I Human chr7 + 128461093 128461093 128461093 CTAGCTACCAAAGGGGTTGAAGTGGGAGGATCACTTGAGCCCAGGAGTTTGAGGCTGCAGTGAGC CTAGCTACCAAAGGGGTTGAAGTGGGAGGATCGCTTGAGCCCAGGAGTTTGAGGCTGCAGTGAGC A G AC010655.2,AC010655.4 Ensembl:ENSG00000240758,Ensembl:ENSG00000273184 lincRNA,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs993986703 Functional Loss SNV dbSNP153 33..33 33 - - - 10518 RMVar_ID_10518 Human_SNP_ID_339591210 A-to-I Human chr7 + 128461307 128461307 128461307 CAGTCTGACCAATATGGTGAAACCCTGTCTCTACTAAAAATACAAAAATTAGCTGGGCATGGTGG CAGTCTGACCAATATGGTGAAACCCTGTCTCTCCTAAAAATACAAAAATTAGCTGGGCATGGTGG A C AC010655.2,AC010655.4 Ensembl:ENSG00000240758,Ensembl:ENSG00000273184 lincRNA,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1352592270 Functional Loss SNV dbSNP153 33..33 33 - - - 10519 RMVar_ID_10519 Human_SNP_ID_339591374 A-to-I Human chr7 + 128462030 128462027 128462038 GCTCTGTCGCCCATGCTGGAGTGCAGTGGCACAATCTCGGCTCACTGCAACCTCTGCCTCTGGGT GCTCTGTCGCCCATGCTGGAGTGCAGTGGTGGCATTGTGGTTCACTGCAACCTCTGCCTCTGGGT CACAATCTCGGC TGGCATTGTGGT AC010655.2,AC010655.4 Ensembl:ENSG00000240758,Ensembl:ENSG00000273184 lincRNA,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs71529427 Functional Loss MNV dbSNP153 30..41 33 - - - Human_RBP_ID_16001335 10520 RMVar_ID_10520 Human_SNP_ID_339593360 A-to-I Human chr7 + 128469454 128469454 128469454 TTGGCTTACTGTAACCTCCACCTCCTGGGTTCAAGCCATTTTCCTGGCTAAGCCTCCCGAGTAGC TTGGCTTACTGTAACCTCCACCTCCTGGGTTCGAGCCATTTTCCTGGCTAAGCCTCCCGAGTAGC A G AC010655.4 Ensembl:ENSG00000273184 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1022799293 Functional Loss SNV dbSNP153 33..33 33 - - - 10521 RMVar_ID_10521 Human_SNP_ID_339593529 A-to-I Human chr7 + 128470169 128470169 128470169 CAAAAATTAGTCGGGCGTGGTGGCACATGCCCATAATCCCAGCTACTCTGGAGGCTGAAGCGGGA CAAAAATTAGTCGGGCGTGGTGGCACATGCCCGTAATCCCAGCTACTCTGGAGGCTGAAGCGGGA A G AC010655.4 Ensembl:ENSG00000273184 lincRNA intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs974465593 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26069075 10522 RMVar_ID_10522 Human_SNP_ID_339593669 A-to-I Human chr7 + 128470722 128470722 128470722 CATGCCCAGCTAATTTTTTTTTATTTTTGTAGAGACACGGACTCCCTATGTTGCTCAGGCTGGTC CATGCCCAGCTAATTTTTTTTTATTTTTGTAGCGACACGGACTCCCTATGTTGCTCAGGCTGGTC A C AC010655.4 Ensembl:ENSG00000273184 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs554022843 Functional Loss SNV dbSNP153 33..33 33 - - - 10523 RMVar_ID_10523 Human_SNP_ID_339593844 A-to-I Human chr7 + 128471471 128471471 128471471 AAACTCCTGAACTCAGGTGATCTGTCAACCTCAGCCTCCCAAAGTGCTGGGATAACAGGCATGAG AAACTCCTGAACTCAGGTGATCTGTCAACCTCGGCCTCCCAAAGTGCTGGGATAACAGGCATGAG A G AC010655.4 Ensembl:ENSG00000273184 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1416942595 Functional Loss SNV dbSNP153 33..33 33 - - - 10524 RMVar_ID_10524 Human_SNP_ID_339596318 A-to-I Human chr7 + 128481691 128481691 128481691 TTGAGACAAGCTCTTGTTCTGTCATCCCGACTAGAGCACAGTGGTGTGCCCATAGCACACTGCAG TTGAGACAAGCTCTTGTTCTGTCATCCCGACTGGAGCACAGTGGTGTGCCCATAGCACACTGCAG A G AC010655.4,METTL2B Ensembl:ENSG00000273184,Ensembl:ENSG00000165055 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1483438567 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3868108 RMVar_hsa_circ_51388,RMVar_hsa_circ_248222,RMVar_hsa_circ_370536 10525 RMVar_ID_10525 Human_SNP_ID_339596328 A-to-I Human chr7 + 128481736 128481736 128481736 GTGCCCATAGCACACTGCAGGCTCAAACTCCTAGGCTCAAGCAATCGTCTCACCTCAGCCTCCCA GTGCCCATAGCACACTGCAGGCTCAAACTCCTGGGCTCAAGCAATCGTCTCACCTCAGCCTCCCA A G AC010655.4,METTL2B Ensembl:ENSG00000273184,Ensembl:ENSG00000165055 lincRNA,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1436831375 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3868108 RMVar_hsa_circ_51388,RMVar_hsa_circ_248222,RMVar_hsa_circ_370536 10526 RMVar_ID_10526 Human_SNP_ID_339597478 A-to-I Human chr7 + 128486195 128486195 128486195 GGGTGCCTGTAATCCCAGCTACTCAGGAAGCTAAGGCAGGAAAATGGCTTGGACCCAGGAGTGGA GGGTGCCTGTAATCCCAGCTACTCAGGAAGCTGAGGCAGGAAAATGGCTTGGACCCAGGAGTGGA A G AC010655.4,METTL2B Ensembl:ENSG00000273184,Ensembl:ENSG00000165055 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs141207475 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3868111,Human_RBP_ID_7691291,Human_RBP_ID_16001478 RMVar_hsa_circ_51388,RMVar_hsa_circ_248222,RMVar_hsa_circ_370536 10527 RMVar_ID_10527 Human_SNP_ID_339598616 A-to-I Human chr7 + 128490974 128490974 128490974 CATGAGGTCAGGAGTTCGATACCAGCCTGACCAATATGGTGAAACCCCGTCTCTACTAAAAATAT CATGAGGTCAGGAGTTCGATACCAGCCTGACCGATATGGTGAAACCCCGTCTCTACTAAAAATAT A G AC010655.4,METTL2B Ensembl:ENSG00000273184,Ensembl:ENSG00000165055 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1258970995 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51388,RMVar_hsa_circ_248224,RMVar_hsa_circ_362652,RMVar_hsa_circ_372716 10528 RMVar_ID_10528 Human_SNP_ID_339598725 A-to-I Human chr7 + 128491386 128491386 128491386 GGGAGGCTAAGACGGGCAGATCATCTGAGGTCAAGAGTTCCAGACCAGCCTGGCCAATATGGTGA GGGAGGCTAAGACGGGCAGATCATCTGAGGTCGAGAGTTCCAGACCAGCCTGGCCAATATGGTGA A G AC010655.4,METTL2B Ensembl:ENSG00000273184,Ensembl:ENSG00000165055 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1207528979 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51388,RMVar_hsa_circ_248224,RMVar_hsa_circ_362652,RMVar_hsa_circ_372716 10529 RMVar_ID_10529 Human_SNP_ID_339600632 A-to-I Human chr7 + 128499427 128499427 128499427 CAGGCTGGAGCGCAATGGCGCGATCTCGGCTCACTGCAACCTCTGCCTCCTGGGTCCACCCACCT CAGGCTGGAGCGCAATGGCGCGATCTCGGCTCTCTGCAACCTCTGCCTCCTGGGTCCACCCACCT A T METTL2B Ensembl:ENSG00000165055 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs990803724 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12616,RMVar_hsa_circ_312621 10530 RMVar_ID_10530 Human_SNP_ID_339601457 A-to-I Human chr7 + 128502621 128502621 128502621 ATCGTGGTCTTTGCTTTAATCTTAGTTCCGCCAGGCACGGTGGCTCACACCTGTAATCCCAGCAC ATCGTGGTCTTTGCTTTAATCTTAGTTCCGCCGGGCACGGTGGCTCACACCTGTAATCCCAGCAC A G METTL2B Ensembl:ENSG00000165055 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1344107166 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8219051 Human_Splice_Rec_920432 10531 RMVar_ID_10531 Human_SNP_ID_339601463 A-to-I Human chr7 + 128502637 128502637 128502637 TAATCTTAGTTCCGCCAGGCACGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGC TAATCTTAGTTCCGCCAGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGC A G METTL2B Ensembl:ENSG00000165055 Protein coding 3'UTR GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line - 24183664,31158229 RNA-Seq:(High) rs1386784188 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8219051 Human_Splice_Rec_920432 10532 RMVar_ID_10532 Human_SNP_ID_339601554 A-to-I Human chr7 + 128502881 128502881 128502881 GATTGCGCCACTGTACTCCAGCCTGGGCAACAAAGCAAGACTCTGTCTCAAAAAAATAAAAATAA GATTGCGCCACTGTACTCCAGCCTGGGCAACAGAGCAAGACTCTGTCTCAAAAAAATAAAAATAA A G METTL2B Ensembl:ENSG00000165055 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1477522225 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_674593 10533 RMVar_ID_10533 Human_SNP_ID_339601576 A-to-I Human chr7 + 128503013 128503013 128503013 GAATTTGGCTGGGTGCGGTAGCTCATGCCTGTAATCCCAACACTTTGGGAGGCTGAGGCAGGTGG GAATTTGGCTGGGTGCGGTAGCTCATGCCTGTGATCCCAACACTTTGGGAGGCTGAGGCAGGTGG A G METTL2B Ensembl:ENSG00000165055 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1036758689 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8219054 10534 RMVar_ID_10534 Human_SNP_ID_339601608 A-to-I Human chr7 + 128503123 128503123 128503123 ACCTCGTCTCCACTAAAAATACCAAAAAAAATAGCTGGGCATGGTGGCATGCGCCTGTAGTCCCC ACCTCGTCTCCACTAAAAATACCAAAAAAAATGGCTGGGCATGGTGGCATGCGCCTGTAGTCCCC A G METTL2B Ensembl:ENSG00000165055 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1400005385 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17712097,Human_RBP_ID_18091727 10535 RMVar_ID_10535 Human_SNP_ID_339601621 A-to-I Human chr7 + 128503181 128503181 128503181 AGTCCCCTGTAGTCCCAGCTACTCGGGAGGCTAAGGCAGGAGAATCGTTTGAACCTGGGAGGCAG AGTCCCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGTTTGAACCTGGGAGGCAG A G METTL2B Ensembl:ENSG00000165055 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs534603716 Functional Loss SNV dbSNP153 33..33 33 - - - 10536 RMVar_ID_10536 Human_SNP_ID_339601634 A-to-I Human chr7 + 128503235 128503235 128503235 CTGGGAGGCAGAGGTTGCAGTGAGCCGAGATCATGTCACTGCATTCCAGCCTGGGCAACAGAGGA CTGGGAGGCAGAGGTTGCAGTGAGCCGAGATCGTGTCACTGCATTCCAGCCTGGGCAACAGAGGA A G METTL2B Ensembl:ENSG00000165055 Protein coding 3'UTR GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1382725014 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10371666,Human_RBP_ID_16001696,Human_RBP_ID_23071913,Human_RBP_ID_26134271,Human_RBP_ID_26543020 10537 RMVar_ID_10537 Human_SNP_ID_339601698 A-to-I Human chr7 + 128503458 128503458 128503458 TTAGATGCTTTTTTTTTTTTTTTTTAGGAGACAGGGCTCTCACTTTGTTGCCCAGGCTGGAGTTC TTAGATGCTTTTTTTTTTTTTTTTTAGGAGACGGGGCTCTCACTTTGTTGCCCAGGCTGGAGTTC A G METTL2B Ensembl:ENSG00000165055 Protein coding 3'UTR GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-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 10538 RMVar_ID_10538 Human_SNP_ID_339601699 A-to-I Human chr7 + 128503467 128503463 128503468 TTTTTTTTTTTTTTTTAGGAGACAGGGCTCTCACTTTGTTGCCCAGGCTGGAGTTCAGTGGTGCA TTTTTTTTTTTTTTTTAGGAGACAGGGCT_____TTTGTTGCCCAGGCTGGAGTTCAGTGGTGCA TCTCAC T METTL2B Ensembl:ENSG00000165055 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1446236542 Functional Loss DEL dbSNP153 30..34 33 - - - Human_RBP_ID_254472,Human_RBP_ID_794453,Human_RBP_ID_7691336,Human_RBP_ID_26550789 Human_miRNA_ID_59559,Human_miRNA_ID_1591663 10539 RMVar_ID_10539 Human_SNP_ID_339601701 A-to-I Human chr7 + 128503467 128503465 128503467 TTTTTTTTTTTTTTTTAGGAGACAGGGCTCTCACTTTGTTGCCCAGGCTGGAGTTCAGTGGTGCA TTTTTTTTTTTTTTTTAGGAGACAGGGCTCT__CTTTGTTGCCCAGGCTGGAGTTCAGTGGTGCA TCA T METTL2B Ensembl:ENSG00000165055 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1353958627 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_254472,Human_RBP_ID_794453,Human_RBP_ID_7691336,Human_RBP_ID_26550789 Human_miRNA_ID_59559,Human_miRNA_ID_1591663 10540 RMVar_ID_10540 Human_SNP_ID_339601768 A-to-I Human chr7 + 128503740 128503740 128503740 GACTTTTCGACCAGGCATGGCGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCTGAGGTGGGC GACTTTTCGACCAGGCATGGCGGCTCACGCCTCTAATCCCAGCACTTTGGGAGGCTGAGGTGGGC A C METTL2B Ensembl:ENSG00000165055 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs377756643 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_794454 10541 RMVar_ID_10541 Human_SNP_ID_339601769 A-to-I Human chr7 + 128503740 128503740 128503740 GACTTTTCGACCAGGCATGGCGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCTGAGGTGGGC GACTTTTCGACCAGGCATGGCGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGC A G METTL2B Ensembl:ENSG00000165055 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs377756643 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_794454 10542 RMVar_ID_10542 Human_SNP_ID_339601812 A-to-I Human chr7 + 128503887 128503887 128503887 CGGCATGGTTGTGGGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGTAGGAGAATTGCTTGAA CGGCATGGTTGTGGGCGCCTGTAATCCCAGCTGCTCAGGAGGCTGAGGTAGGAGAATTGCTTGAA A G METTL2B Ensembl:ENSG00000165055 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1477808024 Functional Loss SNV dbSNP153 33..33 33 - - - 10543 RMVar_ID_10543 Human_SNP_ID_339601813 A-to-I Human chr7 + 128503891 128503891 128503891 ATGGTTGTGGGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGTAGGAGAATTGCTTGAACCTG ATGGTTGTGGGCGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGTAGGAGAATTGCTTGAACCTG A G METTL2B Ensembl:ENSG00000165055 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1168963181 Functional Loss SNV dbSNP153 33..33 33 - - - 10544 RMVar_ID_10544 Human_SNP_ID_339601825 A-to-I Human chr7 + 128503980 128503979 128503981 AGATGGTGCCATTGCACTCCAGCCTGGGCGACAAGAGCGAAACTGCATCTCAAAAACAAAGATGC AGATGGTGCCATTGCACTCCAGCCTGGGCGAC__GAGCGAAACTGCATCTCAAAAACAAAGATGC CAA C METTL2B Ensembl:ENSG00000165055 Protein coding 3'UTR GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 29129909,30559470 RNA-Seq:(High) rs923489374 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_7691342 10545 RMVar_ID_10545 Human_SNP_ID_339601826 A-to-I Human chr7 + 128503980 128503980 128503980 AGATGGTGCCATTGCACTCCAGCCTGGGCGACAAGAGCGAAACTGCATCTCAAAAACAAAGATGC AGATGGTGCCATTGCACTCCAGCCTGGGCGACGAGAGCGAAACTGCATCTCAAAAACAAAGATGC A G METTL2B Ensembl:ENSG00000165055 Protein coding 3'UTR GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 29129909,30559470 RNA-Seq:(High) rs572876423 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7691342 10546 RMVar_ID_10546 Human_SNP_ID_339601910 A-to-I Human chr7 + 128504371 128504371 128504371 CAAGACCCTGACTTTTTTTTTTTTTTTTTTTGAGATGGAGTTTCGCTCTTGTTGCCCAGGCTGGA CAAGACCCTGACTTTTTTTTTTTTTTTTTTTGTGATGGAGTTTCGCTCTTGTTGCCCAGGCTGGA A T METTL2B Ensembl:ENSG00000165055 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1322032300 Functional Loss SNV dbSNP153 33..33 33 - - - 10547 RMVar_ID_10547 Human_SNP_ID_339602010 A-to-I Human chr7 + 128504698 128504698 128504698 TTTTTAAAAAATGTTAAACATAGGCCGGGTGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGG TTTTTAAAAAATGTTAAACATAGGCCGGGTGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG A G METTL2B Ensembl:ENSG00000165055 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1257880998 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_674596 10548 RMVar_ID_10548 Human_SNP_ID_339602015 A-to-I Human chr7 + 128504714 128504714 128504714 AACATAGGCCGGGTGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGCGG AACATAGGCCGGGTGCAGTGGCTCACGCCTGTCATCCCAGCACTTTGGGAGGCCGAGGTGGGCGG A C METTL2B Ensembl:ENSG00000165055 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs1400695368 Functional Loss SNV dbSNP153 33..33 33 - - - 10549 RMVar_ID_10549 Human_SNP_ID_339602029 A-to-I Human chr7 + 128504760 128504760 128504760 GGGAGGCCGAGGTGGGCGGATCATTTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACTTAATGA GGGAGGCCGAGGTGGGCGGATCATTTGAGGTCGGGAGTTCGAGACCAGCCTGGCCAACTTAATGA A G METTL2B Ensembl:ENSG00000165055 Protein coding 3'UTR GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829 ASD brains,Fragile X samples from UC Davis FXTAS brain repository;Bronchiolar epithelium,BEP2D cell line - 30559470,31158229 RNA-Seq:(High) rs1406894768 Functional Loss SNV dbSNP153 33..33 33 - - - 10550 RMVar_ID_10550 Human_SNP_ID_339602339 A-to-I Human chr7 + 128506026 128506026 128506026 TTTTGTATTTTTTGTAGAGACAGGGTTTCACCATGTGTCCCAGGCTGGTCTTGAGCTCCTGAGCT TTTTGTATTTTTTGTAGAGACAGGGTTTCACCGTGTGTCCCAGGCTGGTCTTGAGCTCCTGAGCT A G METTL2B Ensembl:ENSG00000165055 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs148919764 Functional Loss SNV dbSNP153 33..33 33 - - - 10551 RMVar_ID_10551 Human_SNP_ID_339607875 A-to-I Human chr7 - 128528020 128528020 128528020 TAATTAGCTGGGCGTGGCGGCGGGCACCTGTAATCCCAGCTAGTCGGGAGACTGAGGCAGGAGAA TAATTAGCTGGGCGTGGCGGCGGGCACCTGTAGTCCCAGCTAGTCGGGAGACTGAGGCAGGAGAA T C AC090114.2 Ensembl:ENSG00000273270 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1314189133 Functional Loss SNV dbSNP153 33..33 33 - - - 10552 RMVar_ID_10552 Human_SNP_ID_339607877 A-to-I Human chr7 - 128528027 128528027 128528027 ATTTTTTTAATTAGCTGGGCGTGGCGGCGGGCACCTGTAATCCCAGCTAGTCGGGAGACTGAGGC ATTTTTTTAATTAGCTGGGCGTGGCGGCGGGCGCCTGTAATCCCAGCTAGTCGGGAGACTGAGGC T C AC090114.2 Ensembl:ENSG00000273270 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1341008421 Functional Loss SNV dbSNP153 33..33 33 - - - 10553 RMVar_ID_10553 Human_SNP_ID_339607894 A-to-I Human chr7 - 128528090 128528090 128528090 ACGAGGTCAGGAGATTGAGATCCAACCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATAT ACGAGGTCAGGAGATTGAGATCCAACCTGGCCGACATGGTGAAACCCCATCTCTACTAAAAATAT T C AC090114.2 Ensembl:ENSG00000273270 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1258265588 Functional Loss SNV dbSNP153 33..33 33 - - - 10554 RMVar_ID_10554 Human_SNP_ID_339608281 A-to-I Human chr7 - 128529388 128529388 128529388 GAATTCCTGACCTCAGGTGATCCGCCCATCTCAGCCTCCCAAAGTGCTGGGATTTCAAGCGTTAG GAATTCCTGACCTCAGGTGATCCGCCCATCTCGGCCTCCCAAAGTGCTGGGATTTCAAGCGTTAG T C AC090114.2 Ensembl:ENSG00000273270 lincRNA exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs558171748 Functional Loss SNV dbSNP153 33..33 33 - - - 10555 RMVar_ID_10555 Human_SNP_ID_339608292 A-to-I Human chr7 - 128529440 128529440 128529440 TTTTTTTTTTTTGGTGGAGTCGAGGTTTTGCCATGTTGGCCACGTTGGTCTCGAATTCCTGACCT TTTTTTTTTTTTGGTGGAGTCGAGGTTTTGCCGTGTTGGCCACGTTGGTCTCGAATTCCTGACCT T C AC090114.2 Ensembl:ENSG00000273270 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs925145666 Functional Loss SNV dbSNP153 33..33 33 - - - 10556 RMVar_ID_10556 Human_SNP_ID_339612419 A-to-I Human chr7 + 128545265 128545265 128545265 AACCCCAACTCTACTAAAAATACAAAAAAATTAGCTGGGCGTGTTGGTGGGCACCTGTAATTCCA AACCCCAACTCTACTAAAAATACAAAAAAATTGGCTGGGCGTGTTGGTGGGCACCTGTAATTCCA A G AC090114.3 Ensembl:ENSG00000280828 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs373037756 Functional Loss SNV dbSNP153 33..33 33 - - - 10557 RMVar_ID_10557 Human_SNP_ID_339612936 A-to-I Human chr7 + 128547635 128547635 128547635 CTCCCGGCCATTTTTTGTATTTTAGTAGAGACAGGATTTTGCCATGTTGGCTGGGCTGGTCTCCA CTCCCGGCCATTTTTTGTATTTTAGTAGAGACGGGATTTTGCCATGTTGGCTGGGCTGGTCTCCA A G AC090114.3 Ensembl:ENSG00000280828 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs868117397 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16001963,Human_RBP_ID_23315110 10558 RMVar_ID_10558 Human_SNP_ID_339612944 A-to-I Human chr7 + 128547680 128547679 128547681 GTTGGCTGGGCTGGTCTCCAACTTCTGACTGCAAGTGATCTGCCTGCCTTGGCCTCCCAAAGTGT GTTGGCTGGGCTGGTCTCCAACTTCTGACTGC__GTGATCTGCCTGCCTTGGCCTCCCAAAGTGT CAA C AC090114.3 Ensembl:ENSG00000280828 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1217247481 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_16001965,Human_RBP_ID_23315686 10559 RMVar_ID_10559 Human_SNP_ID_339615583 A-to-I Human chr7 + 128558458 128558458 128558458 ATTTTTTAGGCAGGGCATGGTGGCTCATGCCTATAATCTCTGCACTTTGGGAGGCCAAGGTGGGT ATTTTTTAGGCAGGGCATGGTGGCTCATGCCTGTAATCTCTGCACTTTGGGAGGCCAAGGTGGGT A G AC090114.3 Ensembl:ENSG00000280828 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1477957047 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16272675,Human_RBP_ID_18109399 10560 RMVar_ID_10560 Human_SNP_ID_339615676 A-to-I Human chr7 + 128558941 128558940 128558942 GCCTGGCTAATTTTGGAAGTCTTAGTAGAGACAGGGTGTTGTTGTGCTGCCCAGGTCTCGAGCTC GCCTGGCTAATTTTGGAAGTCTTAGTAGAGAC__GGTGTTGTTGTGCTGCCCAGGTCTCGAGCTC CAG C AC090114.3 Ensembl:ENSG00000280828 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1185826398 Functional Loss DEL dbSNP153 33..34 33 - - - 10561 RMVar_ID_10561 Human_SNP_ID_339615677 A-to-I Human chr7 + 128558941 128558941 128558941 GCCTGGCTAATTTTGGAAGTCTTAGTAGAGACAGGGTGTTGTTGTGCTGCCCAGGTCTCGAGCTC GCCTGGCTAATTTTGGAAGTCTTAGTAGAGACGGGGTGTTGTTGTGCTGCCCAGGTCTCGAGCTC A G AC090114.3 Ensembl:ENSG00000280828 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs537125492 Functional Loss SNV dbSNP153 33..33 33 - - - 10562 RMVar_ID_10562 Human_SNP_ID_339622207 A-to-I Human chr7 + 128583635 128583635 128583635 GCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGGACTACAGACAGACGCCACCAAGCCC GCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTCGCTGGGGACTACAGACAGACGCCACCAAGCCC A C AC090114.3,AC108010.1 Ensembl:ENSG00000280828,Ensembl:ENSG00000242588 Pseudogene,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1193008065 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_248228,RMVar_hsa_circ_248226,RMVar_hsa_circ_293771,RMVar_hsa_circ_90953,RMVar_hsa_circ_248229,RMVar_hsa_circ_29626,RMVar_hsa_circ_283799,RMVar_hsa_circ_327891,RMVar_hsa_circ_337970,RMVar_hsa_circ_302679,RMVar_hsa_circ_38391,RMVar_hsa_circ_248230 10563 RMVar_ID_10563 Human_SNP_ID_339633794 A-to-I Human chr7 + 128632166 128632166 128632166 CTAGCAGTTTGGAAGGCTGACGCACATGGACTACTTGAGGTCAGGAGTTTGAGACCAGCCTGACC CTAGCAGTTTGGAAGGCTGACGCACATGGACTGCTTGAGGTCAGGAGTTTGAGACCAGCCTGACC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs914626535 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_248229 10564 RMVar_ID_10564 Human_SNP_ID_339634262 A-to-I Human chr7 + 128633804 128633804 128633804 AAAAAAAACCAGGTGTTGTGGCATGCAGCTGTAGTCTCAGTTCCTAGGGAGGCTGAGGCGGGAGG AAAAAAAACCAGGTGTTGTGGCATGCAGCTGTGGTCTCAGTTCCTAGGGAGGCTGAGGCGGGAGG A G LINC01000,LINC01000:2 RNACentral:URS00008B2CF5,RNACentral:URS00008BAD4F lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978467504 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_248229 10565 RMVar_ID_10565 Human_SNP_ID_339638800 A-to-I Human chr7 + 128653430 128653430 128653430 GAGAACAGCCTCTGCAGGCCCCGCCCTTGCCTACCAGGGGCCTCTCCAGGCGCAGCTCTTGCCCC GAGAACAGCCTCTGCAGGCCCCGCCCTTGCCTGCCAGGGGCCTCTCCAGGCGCAGCTCTTGCCCC A G LINC01000,LINC01000:2 RNACentral:URS00008C0C4E,RNACentral:URS000075B9E1 lincRNA,lincRNA intron,exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1167355753 Functional Loss SNV dbSNP153 33..33 33 - - - 10566 RMVar_ID_10566 Human_SNP_ID_339638805 A-to-I Human chr7 + 128653445 128653445 128653445 AGGCCCCGCCCTTGCCTACCAGGGGCCTCTCCAGGCGCAGCTCTTGCCCCCACGGCGGCCTCCCG AGGCCCCGCCCTTGCCTACCAGGGGCCTCTCCGGGCGCAGCTCTTGCCCCCACGGCGGCCTCCCG A G LINC01000,LINC01000:2 RNACentral:URS00008C0C4E,RNACentral:URS000075B9E1 lincRNA,lincRNA intron,exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1430857713 Functional Loss SNV dbSNP153 33..33 33 - - - 10567 RMVar_ID_10567 Human_SNP_ID_339638831 A-to-I Human chr7 + 128653510 128653510 128653510 GGGCCAAGTCCCTGCCTGCCTCCCAGCAGCCCACGTGCGGCCCAGCTCCTCTCTCACGGTGGCCT GGGCCAAGTCCCTGCCTGCCTCCCAGCAGCCCGCGTGCGGCCCAGCTCCTCTCTCACGGTGGCCT A G LINC01000,LINC01000:2 RNACentral:URS00008C0C4E,RNACentral:URS000075B9E1 lincRNA,lincRNA intron,exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1454333439 Functional Loss SNV dbSNP153 33..33 33 - - - 10568 RMVar_ID_10568 Human_SNP_ID_339638905 A-to-I Human chr7 + 128653713 128653713 128653713 GCCCCTGCCTCAACAGGCCACCGTGAGGGAGGAGCAGGGTCGCACGCGGGCTGCTGGGAGGTAGG GCCCCTGCCTCAACAGGCCACCGTGAGGGAGGGGCAGGGTCGCACGCGGGCTGCTGGGAGGTAGG A G LINC01000,LINC01000:2 RNACentral:URS0000D58990,RNACentral:URS000075B9E1 lincRNA,lincRNA intron,exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1190672874 Functional Loss SNV dbSNP153 33..33 33 - - - 10569 RMVar_ID_10569 Human_SNP_ID_339638907 A-to-I Human chr7 + 128653716 128653716 128653716 CCTGCCTCAACAGGCCACCGTGAGGGAGGAGCAGGGTCGCACGCGGGCTGCTGGGAGGTAGGCAG CCTGCCTCAACAGGCCACCGTGAGGGAGGAGCGGGGTCGCACGCGGGCTGCTGGGAGGTAGGCAG A G LINC01000,LINC01000:2 RNACentral:URS0000D58990,RNACentral:URS000075B9E1 lincRNA,lincRNA intron,exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1247658182 Functional Loss SNV dbSNP153 33..33 33 - - - 10570 RMVar_ID_10570 Human_SNP_ID_339638912 A-to-I Human chr7 + 128653724 128653724 128653724 AACAGGCCACCGTGAGGGAGGAGCAGGGTCGCACGCGGGCTGCTGGGAGGTAGGCAGGGACTTGG AACAGGCCACCGTGAGGGAGGAGCAGGGTCGCGCGCGGGCTGCTGGGAGGTAGGCAGGGACTTGG A G LINC01000,LINC01000:2 RNACentral:URS0000D58990,RNACentral:URS000075B9E1 lincRNA,lincRNA intron,exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1340736765 Functional Loss SNV dbSNP153 33..33 33 - - - 10571 RMVar_ID_10571 Human_SNP_ID_339638922 A-to-I Human chr7 + 128653743 128653743 128653743 GGAGCAGGGTCGCACGCGGGCTGCTGGGAGGTAGGCAGGGACTTGGGCCTGGGAGGTCGCGGTGG GGAGCAGGGTCGCACGCGGGCTGCTGGGAGGTGGGCAGGGACTTGGGCCTGGGAGGTCGCGGTGG A G LINC01000,LINC01000:2 RNACentral:URS0000D58990,RNACentral:URS000075B9E1 lincRNA,lincRNA intron,exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1421638897 Functional Loss SNV dbSNP153 33..33 33 - - - 10572 RMVar_ID_10572 Human_SNP_ID_339638923 A-to-I Human chr7 + 128653747 128653747 128653747 CAGGGTCGCACGCGGGCTGCTGGGAGGTAGGCAGGGACTTGGGCCTGGGAGGTCGCGGTGGGGCG CAGGGTCGCACGCGGGCTGCTGGGAGGTAGGCCGGGACTTGGGCCTGGGAGGTCGCGGTGGGGCG A C LINC01000,LINC01000:2 RNACentral:URS0000D58990,RNACentral:URS000075B9E1 lincRNA,lincRNA intron,exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1474718296 Functional Loss SNV dbSNP153 33..33 33 - - - 10573 RMVar_ID_10573 Human_SNP_ID_339638924 A-to-I Human chr7 + 128653747 128653747 128653747 CAGGGTCGCACGCGGGCTGCTGGGAGGTAGGCAGGGACTTGGGCCTGGGAGGTCGCGGTGGGGCG CAGGGTCGCACGCGGGCTGCTGGGAGGTAGGCGGGGACTTGGGCCTGGGAGGTCGCGGTGGGGCG A G LINC01000,LINC01000:2 RNACentral:URS0000D58990,RNACentral:URS000075B9E1 lincRNA,lincRNA intron,exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1474718296 Functional Loss SNV dbSNP153 33..33 33 - - - 10574 RMVar_ID_10574 Human_SNP_ID_339639534 A-to-I Human chr7 + 128655750 128655750 128655750 GGTGGGAAGAGTTTGCAGTGAGCCAAGATCGCACCACTGCACTCCAGCCTGGGCGACAGAGCAAG GGTGGGAAGAGTTTGCAGTGAGCCAAGATCGCGCCACTGCACTCCAGCCTGGGCGACAGAGCAAG A G LINC01000 RNACentral:URS000075B9E1 lincRNA exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1380503874 Functional Loss SNV dbSNP153 33..33 33 - - - 10575 RMVar_ID_10575 Human_SNP_ID_339639676 A-to-I Human chr7 + 128656160 128656160 128656160 GTCAGGGCAGGGGCAGCAGCAGTGGACCCGCTATGCACACATCGTCTTCTCCAAGGTTTGTGTGC GTCAGGGCAGGGGCAGCAGCAGTGGACCCGCTCTGCACACATCGTCTTCTCCAAGGTTTGTGTGC A C LINC01000 RNACentral:URS000075B9E1 lincRNA exon GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1010947307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1681373,Human_RBP_ID_23315687,Human_RBP_ID_27528280 10576 RMVar_ID_10576 Human_SNP_ID_339639677 A-to-I Human chr7 + 128656160 128656160 128656160 GTCAGGGCAGGGGCAGCAGCAGTGGACCCGCTATGCACACATCGTCTTCTCCAAGGTTTGTGTGC GTCAGGGCAGGGGCAGCAGCAGTGGACCCGCTGTGCACACATCGTCTTCTCCAAGGTTTGTGTGC A G LINC01000 RNACentral:URS000075B9E1 lincRNA exon GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1010947307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1681373,Human_RBP_ID_23315687,Human_RBP_ID_27528280 10577 RMVar_ID_10577 Human_SNP_ID_339639706 A-to-I Human chr7 + 128656257 128656257 128656257 CAGTTGGCACCTGCCCCAGTCCAGCCTCTGGGAACCATGCAGCAGCTCCCAGCGGCCCTGCACCC CAGTTGGCACCTGCCCCAGTCCAGCCTCTGGGGACCATGCAGCAGCTCCCAGCGGCCCTGCACCC A G LINC01000 RNACentral:URS000075B9E1 lincRNA exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1307044646 Functional Loss SNV dbSNP153 33..33 33 - - - 10578 RMVar_ID_10578 Human_SNP_ID_339640573 A-to-I Human chr7 + 128659175 128659175 128659175 TGGAGGGCAGTGGTGTGATCTCGGCTCACTGCAACCTCTGCTTCATGGTTTAATTGATTCTCCTG TGGAGGGCAGTGGTGTGATCTCGGCTCACTGCGACCTCTGCTTCATGGTTTAATTGATTCTCCTG A G LINC01000,LINC01000:2 RNACentral:URS000075B9E1,RNACentral:URS0000D5E09A lincRNA,lincRNA exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1314412167 Functional Loss SNV dbSNP153 33..33 33 - - - 10579 RMVar_ID_10579 Human_SNP_ID_339640578 A-to-I Human chr7 + 128659187 128659187 128659187 GTGTGATCTCGGCTCACTGCAACCTCTGCTTCATGGTTTAATTGATTCTCCTGCCTCAGCCCCCT GTGTGATCTCGGCTCACTGCAACCTCTGCTTCGTGGTTTAATTGATTCTCCTGCCTCAGCCCCCT A G LINC01000,LINC01000:2 RNACentral:URS000075B9E1,RNACentral:URS0000D5E09A lincRNA,lincRNA exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1262521755 Functional Loss SNV dbSNP153 33..33 33 - - - 10580 RMVar_ID_10580 Human_SNP_ID_339640597 A-to-I Human chr7 + 128659260 128659260 128659260 GGGATTACAGGCACCCGCCACCACACCTGGTTAATTTTTTGCATTTTTAGAAGGCGTGGGTTTTT GGGATTACAGGCACCCGCCACCACACCTGGTTTATTTTTTGCATTTTTAGAAGGCGTGGGTTTTT A T LINC01000,LINC01000:2 RNACentral:URS000075B9E1,RNACentral:URS0000D5E09A lincRNA,lincRNA exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1292947184 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16002685 10581 RMVar_ID_10581 Human_SNP_ID_339640599 A-to-I Human chr7 + 128659276 128659276 128659276 GCCACCACACCTGGTTAATTTTTTGCATTTTTAGAAGGCGTGGGTTTTTGCCATGTTGGCCTGGC GCCACCACACCTGGTTAATTTTTTGCATTTTTTGAAGGCGTGGGTTTTTGCCATGTTGGCCTGGC A T LINC01000,LINC01000:2 RNACentral:URS000075B9E1,RNACentral:URS0000D5E09A lincRNA,lincRNA exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1028151249 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16002685 10582 RMVar_ID_10582 Human_SNP_ID_339640605 A-to-I Human chr7 + 128659296 128659296 128659296 TTTTGCATTTTTAGAAGGCGTGGGTTTTTGCCATGTTGGCCTGGCTGGACTTGACCTCCTGACCT TTTTGCATTTTTAGAAGGCGTGGGTTTTTGCCGTGTTGGCCTGGCTGGACTTGACCTCCTGACCT A G LINC01000,LINC01000:2 RNACentral:URS000075B9E1,RNACentral:URS0000D5E09A lincRNA,lincRNA exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1431877292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4923938,Human_RBP_ID_16002686,Human_RBP_ID_22833168,Human_RBP_ID_26069843 10583 RMVar_ID_10583 Human_SNP_ID_339640615 A-to-I Human chr7 + 128659357 128659357 128659357 ACCTCAAGTGATCCACCCTCCTTGGCCTCCCAAAATGCTGGGATTACAGGCATGAGCCACCACAC ACCTCAAGTGATCCACCCTCCTTGGCCTCCCAGAATGCTGGGATTACAGGCATGAGCCACCACAC A G LINC01000,LINC01000:2 RNACentral:URS000075B9E1,RNACentral:URS0000D5E09A lincRNA,lincRNA exon,intron GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs1278094218 Functional Loss SNV dbSNP153 33..33 33 - - - 10584 RMVar_ID_10584 Human_SNP_ID_339640675 A-to-I Human chr7 + 128659613 128659613 128659613 AGCTGAGCATGGTGGCACGCACCTGTAGTCCCAGCTACCTGGGATGCTGAGGTGGGAGGATCACT AGCTGAGCATGGTGGCACGCACCTGTAGTCCCGGCTACCTGGGATGCTGAGGTGGGAGGATCACT A G LINC01000,LINC01000:2 RNACentral:URS000075B9E1,RNACentral:URS0000D5E09A lincRNA,lincRNA exon,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1461548099 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27528281 10585 RMVar_ID_10585 Human_SNP_ID_339640676 A-to-I Human chr7 + 128659617 128659617 128659617 GAGCATGGTGGCACGCACCTGTAGTCCCAGCTACCTGGGATGCTGAGGTGGGAGGATCACTTGAG GAGCATGGTGGCACGCACCTGTAGTCCCAGCTGCCTGGGATGCTGAGGTGGGAGGATCACTTGAG A G LINC01000,LINC01000:2 RNACentral:URS000075B9E1,RNACentral:URS0000D5E09A lincRNA,lincRNA exon,intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs764556799 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27528281 10586 RMVar_ID_10586 Human_SNP_ID_339643500 A-to-I Human chr7 + 128671253 128671253 128671253 GTTGAGACGGGGTTTCACCCGTTGACCAGGCTAGTCTCGAACACCTGACCTCAGGCGATCCACCC GTTGAGACGGGGTTTCACCCGTTGACCAGGCTCGTCTCGAACACCTGACCTCAGGCGATCCACCC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1218295416 Functional Loss SNV dbSNP153 33..33 33 - - - 10587 RMVar_ID_10587 Human_SNP_ID_339644897 A-to-I Human chr7 + 128676099 128676099 128676099 TGGAGTGCAGTGGCGGGATCTCGGCTCACTGCAAGCCCCGCCTCCCGGGTTCACGCCATTCACCG TGGAGTGCAGTGGCGGGATCTCGGCTCACTGCCAGCCCCGCCTCCCGGGTTCACGCCATTCACCG A C FAM71F2 Ensembl:ENSG00000205085 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1309712995 Functional Loss SNV dbSNP153 33..33 33 - - - 10588 RMVar_ID_10588 Human_SNP_ID_339647050 A-to-I Human chr7 + 128683495 128683495 128683495 TATTTATTTATTTATTTATTTATTTTGGAGATAGAGTCTTGCTCTGTCTCCAGGCTGGAGTACAG TATTTATTTATTTATTTATTTATTTTGGAGATGGAGTCTTGCTCTGTCTCCAGGCTGGAGTACAG A G FAM71F2 Ensembl:ENSG00000205085 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs961910917 Functional Loss SNV dbSNP153 33..33 33 - - - 10589 RMVar_ID_10589 Human_SNP_ID_339656926 A-to-I Human chr7 + 128724271 128724271 128724271 GACCTAAAGTGATCCACCTGTCTCAGCCTCCCAAAGTGCCAGGACTACAGGCGTGAGCCACTGTG GACCTAAAGTGATCCACCTGTCTCAGCCTCCCTAAGTGCCAGGACTACAGGCGTGAGCCACTGTG A T FAM71F1 Ensembl:ENSG00000135248 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs556183209 Functional Loss SNV dbSNP153 33..33 33 - - - 10590 RMVar_ID_10590 Human_SNP_ID_339661056 A-to-I Human chr7 + 128742598 128742598 128742598 ATTGAAAGTTTGGGCCATGTATTGCTCGCAATACTGGTCCAATGGATACACTATGGACACTAAGG ATTGAAAGTTTGGGCCATGTATTGCTCGCAATGCTGGTCCAATGGATACACTATGGACACTAAGG A G CALU Ensembl:ENSG00000128595 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs994742416 Functional Loss SNV dbSNP153 33..33 33 - - - 10591 RMVar_ID_10591 Human_SNP_ID_339663096 A-to-I Human chr7 + 128751086 128751086 128751086 CCGAGGCAGGCAGTTTATGAGGTCAAGAGATCAAGACCATCCTGGCCAATATGGTGAAATCCCAT CCGAGGCAGGCAGTTTATGAGGTCAAGAGATCTAGACCATCCTGGCCAATATGGTGAAATCCCAT A T CALU Ensembl:ENSG00000128595 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs756488303 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_337851,RMVar_hsa_circ_351004,RMVar_hsa_circ_248241 10592 RMVar_ID_10592 Human_SNP_ID_339663527 A-to-I Human chr7 + 128752819 128752819 128752819 AGATTCTCCTGCCTCAGCCTCCTGAATAGCTGAGATTACAGGCATGCGCCACCATGCCCGGCTAA AGATTCTCCTGCCTCAGCCTCCTGAATAGCTGGGATTACAGGCATGCGCCACCATGCCCGGCTAA A G CALU Ensembl:ENSG00000128595 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs532683680 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_337851,RMVar_hsa_circ_351004,RMVar_hsa_circ_248241 10593 RMVar_ID_10593 Human_SNP_ID_339663543 A-to-I Human chr7 + 128752885 128752885 128752885 TTTTGTGTTTTTAGTAGAGACTGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAATTCCTCACCT TTTTGTGTTTTTAGTAGAGACTGGGTTTCACCGTGTTGGCCAGGCTGGTCTCGAATTCCTCACCT A G CALU Ensembl:ENSG00000128595 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1158474347 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_337851,RMVar_hsa_circ_351004,RMVar_hsa_circ_248241 10594 RMVar_ID_10594 Human_SNP_ID_339665953 A-to-I Human chr7 + 128762744 128762744 128762744 GCTGGAGTGCAGTGGCGTGATCTCCACTCACTACAATCTCTGCCTCCCAGGTTCAGGCGATTCTT GCTGGAGTGCAGTGGCGTGATCTCCACTCACTGCAATCTCTGCCTCCCAGGTTCAGGCGATTCTT A G CALU Ensembl:ENSG00000128595 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1258668568 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97215,RMVar_hsa_circ_248245,RMVar_hsa_circ_81132,RMVar_hsa_circ_248244 10595 RMVar_ID_10595 Human_SNP_ID_339666338 A-to-I Human chr7 + 128764413 128764413 128764413 GTACCACTGCACTCCAGCCTGGGCAACAGAGCAAGACCCTGTCTCAGAAGAAAAAAGAATAATCT GTACCACTGCACTCCAGCCTGGGCAACAGAGCGAGACCCTGTCTCAGAAGAAAAAAGAATAATCT A G CALU Ensembl:ENSG00000128595 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1397674323 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97215,RMVar_hsa_circ_248245,RMVar_hsa_circ_81132,RMVar_hsa_circ_248244 10596 RMVar_ID_10596 Human_SNP_ID_339666530 A-to-I Human chr7 + 128765149 128765149 128765149 ATTGCCCAGGCTGGTCTGGAAATCCTGGGCTCAAGAGCTCTACCTGCCTTGGCCTCCCAAAGTGC ATTGCCCAGGCTGGTCTGGAAATCCTGGGCTCGAGAGCTCTACCTGCCTTGGCCTCCCAAAGTGC A G CALU Ensembl:ENSG00000128595 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1014219207 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16003645 RMVar_hsa_circ_97215,RMVar_hsa_circ_248245,RMVar_hsa_circ_81132,RMVar_hsa_circ_248244 10597 RMVar_ID_10597 Human_SNP_ID_339667671 A-to-I Human chr7 + 128769613 128769613 128769613 AATGTTCAGGAGAGAGGAAAGAAAAAAAATATATGCTCCACAATTTATATTTAGAGAGAGAACAC AATGTTCAGGAGAGAGGAAAGAAAAAAAATATGTGCTCCACAATTTATATTTAGAGAGAGAACAC A G CALU Ensembl:ENSG00000128595 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs529888427 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_674650,Human_RBP_ID_7691968,Human_RBP_ID_8218514,Human_RBP_ID_8907510,Human_RBP_ID_16003760,Human_RBP_ID_17199284,Human_RBP_ID_17311452,Human_RBP_ID_17424022,Human_RBP_ID_17539361,Human_RBP_ID_18091815,Human_RBP_ID_22407082,Human_RBP_ID_22833180,Human_RBP_ID_24437747,Human_RBP_ID_24514715,Human_RBP_ID_26550792,Human_RBP_ID_26721616 RMVar_hsa_circ_248245,RMVar_hsa_circ_81132 10598 RMVar_ID_10598 Human_SNP_ID_339725529 A-to-I Human chr7 - 128983454 128983454 128983454 TCATGCCAGTAATCCCAGCATTTTGGAGGCCTAGACAGGTGGATCATTTGAGGTCCGGAGTTAGA TCATGCCAGTAATCCCAGCATTTTGGAGGCCTGGACAGGTGGATCATTTGAGGTCCGGAGTTAGA T C TNPO3 Ensembl:ENSG00000064419 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs777114982 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75972,RMVar_hsa_circ_12346,RMVar_hsa_circ_361133,RMVar_hsa_circ_5994,RMVar_hsa_circ_91667,RMVar_hsa_circ_332248,RMVar_hsa_circ_347852,RMVar_hsa_circ_328720,RMVar_hsa_circ_330044,RMVar_hsa_circ_324129,RMVar_hsa_circ_248303,RMVar_hsa_circ_248304,RMVar_hsa_circ_357940,RMVar_hsa_circ_30676,RMVar_hsa_circ_371713,RMVar_hsa_circ_124184,RMVar_hsa_circ_126835,RMVar_hsa_circ_248306,RMVar_hsa_circ_248307,RMVar_hsa_circ_248305,RMVar_hsa_circ_52308,RMVar_hsa_circ_102408,RMVar_hsa_circ_35659,RMVar_hsa_circ_106296,RMVar_hsa_circ_248314,RMVar_hsa_circ_248312,RMVar_hsa_circ_248313,RMVar_hsa_circ_82120,RMVar_hsa_circ_123968,RMVar_hsa_circ_346972,RMVar_hsa_circ_370335,RMVar_hsa_circ_116540,RMVar_hsa_circ_87267,RMVar_hsa_circ_101586,RMVar_hsa_circ_77286,RMVar_hsa_circ_15313,RMVar_hsa_circ_110024,RMVar_hsa_circ_248318,RMVar_hsa_circ_248320,RMVar_hsa_circ_248322,RMVar_hsa_circ_248323,RMVar_hsa_circ_248321,RMVar_hsa_circ_248319,RMVar_hsa_circ_248316,RMVar_hsa_circ_248317,RMVar_hsa_circ_248315,RMVar_hsa_circ_378491,RMVar_hsa_circ_274962,RMVar_hsa_circ_248326,RMVar_hsa_circ_248327,RMVar_hsa_circ_295116,RMVar_hsa_circ_305779,RMVar_hsa_circ_332731,RMVar_hsa_circ_278162,RMVar_hsa_circ_21904,RMVar_hsa_circ_40290,RMVar_hsa_circ_18216,RMVar_hsa_circ_248329,RMVar_hsa_circ_248330,RMVar_hsa_circ_248331,RMVar_hsa_circ_248328 10599 RMVar_ID_10599 Human_SNP_ID_339727975 A-to-I Human chr7 - 128994231 128994231 128994231 ATCACTGGAACCTGGGAGGCGGAGGGTGCAGTAAGCAGAGATCGCACCACTGCACTCCAGCCTGG ATCACTGGAACCTGGGAGGCGGAGGGTGCAGTCAGCAGAGATCGCACCACTGCACTCCAGCCTGG T G TNPO3 Ensembl:ENSG00000064419 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs567723289 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75972,RMVar_hsa_circ_12346,RMVar_hsa_circ_361133,RMVar_hsa_circ_332248,RMVar_hsa_circ_328720,RMVar_hsa_circ_330044,RMVar_hsa_circ_324129,RMVar_hsa_circ_248303,RMVar_hsa_circ_248304,RMVar_hsa_circ_357940,RMVar_hsa_circ_124184,RMVar_hsa_circ_248305,RMVar_hsa_circ_52308,RMVar_hsa_circ_102408,RMVar_hsa_circ_106296,RMVar_hsa_circ_248314,RMVar_hsa_circ_248313,RMVar_hsa_circ_82120,RMVar_hsa_circ_123968,RMVar_hsa_circ_370335,RMVar_hsa_circ_87267,RMVar_hsa_circ_77286,RMVar_hsa_circ_7722,RMVar_hsa_circ_248318,RMVar_hsa_circ_248320,RMVar_hsa_circ_248319,RMVar_hsa_circ_248316,RMVar_hsa_circ_248317,RMVar_hsa_circ_248315,RMVar_hsa_circ_378491,RMVar_hsa_circ_274962,RMVar_hsa_circ_248327,RMVar_hsa_circ_295116,RMVar_hsa_circ_305779,RMVar_hsa_circ_40290,RMVar_hsa_circ_29418,RMVar_hsa_circ_248330,RMVar_hsa_circ_248331,RMVar_hsa_circ_323797,RMVar_hsa_circ_248333,RMVar_hsa_circ_366595,RMVar_hsa_circ_285024,RMVar_hsa_circ_248334,RMVar_hsa_circ_294604,RMVar_hsa_circ_299812,RMVar_hsa_circ_359699,RMVar_hsa_circ_248337,RMVar_hsa_circ_248338,RMVar_hsa_circ_101532,RMVar_hsa_circ_285115,RMVar_hsa_circ_372238,RMVar_hsa_circ_268766,RMVar_hsa_circ_248339,RMVar_hsa_circ_248340 10600 RMVar_ID_10600 Human_SNP_ID_339728968 A-to-I Human chr7 - 128998412 128998412 128998412 AGTTCAAGGCTGCAGTGAGCCATGATTGTGCCACTGTGCTCCAGCCTAGGCGACCCTGTCTCTAA AGTTCAAGGCTGCAGTGAGCCATGATTGTGCCGCTGTGCTCCAGCCTAGGCGACCCTGTCTCTAA T C TNPO3 Ensembl:ENSG00000064419 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1324518824 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75972,RMVar_hsa_circ_12346,RMVar_hsa_circ_361133,RMVar_hsa_circ_332248,RMVar_hsa_circ_330044,RMVar_hsa_circ_324129,RMVar_hsa_circ_248303,RMVar_hsa_circ_248304,RMVar_hsa_circ_124184,RMVar_hsa_circ_248305,RMVar_hsa_circ_52308,RMVar_hsa_circ_102408,RMVar_hsa_circ_106296,RMVar_hsa_circ_248314,RMVar_hsa_circ_248313,RMVar_hsa_circ_82120,RMVar_hsa_circ_370335,RMVar_hsa_circ_87267,RMVar_hsa_circ_77286,RMVar_hsa_circ_7722,RMVar_hsa_circ_248318,RMVar_hsa_circ_248319,RMVar_hsa_circ_248316,RMVar_hsa_circ_248317,RMVar_hsa_circ_248315,RMVar_hsa_circ_378491,RMVar_hsa_circ_248327,RMVar_hsa_circ_295116,RMVar_hsa_circ_305779,RMVar_hsa_circ_40290,RMVar_hsa_circ_29418,RMVar_hsa_circ_248331,RMVar_hsa_circ_323797,RMVar_hsa_circ_248333,RMVar_hsa_circ_366595,RMVar_hsa_circ_299812,RMVar_hsa_circ_359699,RMVar_hsa_circ_248337,RMVar_hsa_circ_248338,RMVar_hsa_circ_101532,RMVar_hsa_circ_285115,RMVar_hsa_circ_372238,RMVar_hsa_circ_268766,RMVar_hsa_circ_271550,RMVar_hsa_circ_248339,RMVar_hsa_circ_248340,RMVar_hsa_circ_278442,RMVar_hsa_circ_328805,RMVar_hsa_circ_333816,RMVar_hsa_circ_272181,RMVar_hsa_circ_248342,RMVar_hsa_circ_248343,RMVar_hsa_circ_248341 10601 RMVar_ID_10601 Human_SNP_ID_339736499 A-to-I Human chr7 - 129031959 129031959 129031959 TGAAAAGCCAGGCGTGATGGCTCATGCCTGTAATCTGACTTATTTGGGAGGCTGAGGCAGGAGGA TGAAAAGCCAGGCGTGATGGCTCATGCCTGTAGTCTGACTTATTTGGGAGGCTGAGGCAGGAGGA T C TNPO3 Ensembl:ENSG00000064419 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1443120671 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_674862,Human_RBP_ID_1330189,Human_RBP_ID_18378109 RMVar_hsa_circ_88277,RMVar_hsa_circ_20170,RMVar_hsa_circ_379085,RMVar_hsa_circ_316036,RMVar_hsa_circ_248347,RMVar_hsa_circ_248348,RMVar_hsa_circ_60372 10602 RMVar_ID_10602 Human_SNP_ID_339737350 A-to-I Human chr7 - 129035386 129035386 129035386 GTTGCCCAGGTTGGTCTTGAGCTCCTAGCTTCAAGTGATCCTCCCACCTCAGCCTCCCAAAGTGC GTTGCCCAGGTTGGTCTTGAGCTCCTAGCTTCCAGTGATCCTCCCACCTCAGCCTCCCAAAGTGC T G TNPO3 Ensembl:ENSG00000064419 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1303094514 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88277,RMVar_hsa_circ_20170,RMVar_hsa_circ_379085,RMVar_hsa_circ_316036,RMVar_hsa_circ_248347,RMVar_hsa_circ_248348,RMVar_hsa_circ_60372 10603 RMVar_ID_10603 Human_SNP_ID_339737375 A-to-I Human chr7 - 129035501 129035501 129035501 ATAAATGGACCTCCCACCACAGCCTCCAAAGTAGCTGGCATTACAAGCATGTACCACCACATCTG ATAAATGGACCTCCCACCACAGCCTCCAAAGTTGCTGGCATTACAAGCATGTACCACCACATCTG T A TNPO3 Ensembl:ENSG00000064419 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs544532075 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_45 RMVar_hsa_circ_88277,RMVar_hsa_circ_20170,RMVar_hsa_circ_379085,RMVar_hsa_circ_316036,RMVar_hsa_circ_248347,RMVar_hsa_circ_248348,RMVar_hsa_circ_60372 10604 RMVar_ID_10604 Human_SNP_ID_339737376 A-to-I Human chr7 - 129035501 129035501 129035501 ATAAATGGACCTCCCACCACAGCCTCCAAAGTAGCTGGCATTACAAGCATGTACCACCACATCTG ATAAATGGACCTCCCACCACAGCCTCCAAAGTGGCTGGCATTACAAGCATGTACCACCACATCTG T C TNPO3 Ensembl:ENSG00000064419 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs544532075 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_45 RMVar_hsa_circ_88277,RMVar_hsa_circ_20170,RMVar_hsa_circ_379085,RMVar_hsa_circ_316036,RMVar_hsa_circ_248347,RMVar_hsa_circ_248348,RMVar_hsa_circ_60372 10605 RMVar_ID_10605 Human_SNP_ID_339737581 A-to-I Human chr7 - 129036228 129036228 129036228 ATACACACAGCTGGGTGCGGTGGCTAACGCCTATAATCCCAGCACTTTGGGAGGCCGAGGTGGGC ATACACACAGCTGGGTGCGGTGGCTAACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGC T C TNPO3 Ensembl:ENSG00000064419 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs200419430 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88277,RMVar_hsa_circ_20170,RMVar_hsa_circ_379085,RMVar_hsa_circ_316036,RMVar_hsa_circ_248347,RMVar_hsa_circ_248348,RMVar_hsa_circ_60372 10606 RMVar_ID_10606 Human_SNP_ID_339744402 A-to-I Human chr7 + 129066405 129066405 129066405 CTCCTTAAACTGAATCCTCCTCTCCAGCTTCTAAATTTCCAGCAGGATGACACAGAAGGGCTTGA CTCCTTAAACTGAATCCTCCTCTCCAGCTTCTGAATTTCCAGCAGGATGACACAGAAGGGCTTGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1193549175 Functional Loss SNV dbSNP153 33..33 33 - - - 10607 RMVar_ID_10607 Human_SNP_ID_339759297 A-to-I Human chr7 + 129127569 129127569 129127569 CTTCCAGGAGTTTGTCAATAAATGCCTCATCAAAAACCCAACGGAGCGGGCGGACCTAAAGATGC CTTCCAGGAGTTTGTCAATAAATGCCTCATCAGAAACCCAACGGAGCGGGCGGACCTAAAGATGC A G AC011005.1 Ensembl:ENSG00000230626 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1267045984 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_921873 10608 RMVar_ID_10608 Human_SNP_ID_339759313 A-to-I Human chr7 + 129127594 129127594 129127594 CTCATCAAAAACCCAACGGAGCGGGCGGACCTAAAGATGCTCACAAACCACGCCTTCATCAAGCG CTCATCAAAAACCCAACGGAGCGGGCGGACCTGAAGATGCTCACAAACCACGCCTTCATCAAGCG A G AC011005.1 Ensembl:ENSG00000230626 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917838477 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_921873 10609 RMVar_ID_10609 Human_SNP_ID_339759336 A-to-I Human chr7 + 129127637 129127637 129127637 CAAACCACGCCTTCATCAAGCGGTCCGAGGTGAAAGAAGCGGATTTTGCCTGCTAGTTGTGTAAA CAAACCACGCCTTCATCAAGCGGTCCGAGGTGGAAGAAGCGGATTTTGCCTGCTAGTTGTGTAAA A G AC011005.1 Ensembl:ENSG00000230626 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs927258983 Functional Loss SNV dbSNP153 33..33 33 - - - 10610 RMVar_ID_10610 Human_SNP_ID_339768540 A-to-I Human chr7 + 129165681 129165681 129165681 TCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGCAGATCATTTGAGGTCAGGAGTTTGAGACT TCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGCAGATCATTTGAGGTCAGGAGTTTGAGACT A G TSPAN33 Ensembl:ENSG00000158457 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs531015534 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5133 10611 RMVar_ID_10611 Human_SNP_ID_339768550 A-to-I Human chr7 + 129165748 129165736 129165748 CCTGGCCAACATGATGAAACCCTGTTTCCACCAAAAATACAAAAATTAGCCGGGTTTGGTGGCGC CCTGGCCAACATGATGAAACC____________AAAATACAAAAATTAGCCGGGTTTGGTGGCGC CCTGTTTCCACCA C TSPAN33 Ensembl:ENSG00000158457 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1218588581 Functional Loss DEL dbSNP153 22..33 33 - - - RMVar_hsa_circ_5133 10612 RMVar_ID_10612 Human_SNP_ID_339768554 A-to-I Human chr7 + 129165748 129165747 129165748 CCTGGCCAACATGATGAAACCCTGTTTCCACCAAAAATACAAAAATTAGCCGGGTTTGGTGGCGC CCTGGCCAACATGATGAAACCCTGTTTCCACC_AAAATACAAAAATTAGCCGGGTTTGGTGGCGC CA C TSPAN33 Ensembl:ENSG00000158457 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1563139330 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_5133 10613 RMVar_ID_10613 Human_SNP_ID_339768632 A-to-I Human chr7 + 129166077 129166044 129166077 TGCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGTGCCTGCCAAACCACGCCCAGCTAATTC _________________________________CAGGTGCCTGCCAAACCACGCCCAGCTAATTC CTGCCTGCCTCAGCCTCCTGAGTAGCTGGGATTA C TSPAN33 Ensembl:ENSG00000158457 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs762845241 Functional Loss DEL dbSNP153 1..33 33 - - - RMVar_hsa_circ_5133 10614 RMVar_ID_10614 Human_SNP_ID_339768634 A-to-I Human chr7 + 129166055 129166055 129166055 GCCTCCTGGGTTCAAGTGAATCTGCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGTGCCTG GCCTCCTGGGTTCAAGTGAATCTGCCTGCCTCCGCCTCCTGAGTAGCTGGGATTACAGGTGCCTG A C TSPAN33 Ensembl:ENSG00000158457 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs544213247 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5133 10615 RMVar_ID_10615 Human_SNP_ID_339768648 A-to-I Human chr7 + 129166120 129166120 129166120 CCAAACCACGCCCAGCTAATTCTTGTATTTTTAGTAAAGATGGGGTTTTGCAATATTGGCCAGGC CCAAACCACGCCCAGCTAATTCTTGTATTTTTTGTAAAGATGGGGTTTTGCAATATTGGCCAGGC A T TSPAN33 Ensembl:ENSG00000158457 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1158545384 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5133 10616 RMVar_ID_10616 Human_SNP_ID_339768650 A-to-I Human chr7 + 129166123 129166123 129166123 AACCACGCCCAGCTAATTCTTGTATTTTTAGTAAAGATGGGGTTTTGCAATATTGGCCAGGCTGG AACCACGCCCAGCTAATTCTTGTATTTTTAGTTAAGATGGGGTTTTGCAATATTGGCCAGGCTGG A T TSPAN33 Ensembl:ENSG00000158457 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1361590883 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5133 10617 RMVar_ID_10617 Human_SNP_ID_339770591 A-to-I Human chr7 + 129174250 129174249 129174250 AAAGTTAGCTAGGTGTGGTGGCACATGTCTGTAATCCCAGCTACTTGGGAGGCTGAGACAGAATC AAAGTTAGCTAGGTGTGGTGGCACATGTCTGT_ATCCCAGCTACTTGGGAGGCTGAGACAGAATC TA T lnc-TSPAN33-2 RNACentral:URS00008B918C lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1448927391 Functional Loss DEL dbSNP153 33..33 33 - - - 10618 RMVar_ID_10618 Human_SNP_ID_339770592 A-to-I Human chr7 + 129174250 129174250 129174250 AAAGTTAGCTAGGTGTGGTGGCACATGTCTGTAATCCCAGCTACTTGGGAGGCTGAGACAGAATC AAAGTTAGCTAGGTGTGGTGGCACATGTCTGTGATCCCAGCTACTTGGGAGGCTGAGACAGAATC A G lnc-TSPAN33-2 RNACentral:URS00008B918C lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1287276741 Functional Loss SNV dbSNP153 33..33 33 - - - 10619 RMVar_ID_10619 Human_SNP_ID_339770892 A-to-I Human chr7 + 129175445 129175445 129175445 TCATTTACAGCTGGGCATGGTGGGTCATACCTATAATCCCAGCAATTTGGGAGGCTGAAGTTGGA TCATTTACAGCTGGGCATGGTGGGTCATACCTGTAATCCCAGCAATTTGGGAGGCTGAAGTTGGA A G lnc-TSPAN33-2 RNACentral:URS00008B918C lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs147158495 Functional Loss SNV dbSNP153 33..33 33 - - - 10620 RMVar_ID_10620 Human_SNP_ID_339780244 A-to-I Human chr7 - 129212712 129212712 129212712 TACCCCCTGCCCCGATGGAGCAGATGCTGCCAACCAGGCTGCAGCTGGCAGGGCAGAAACAAGGA TACCCCCTGCCCCGATGGAGCAGATGCTGCCAGCCAGGCTGCAGCTGGCAGGGCAGAAACAAGGA T C AC011005.4 Ensembl:ENSG00000243230 lincRNA intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs908932266 Functional Loss SNV dbSNP153 33..33 33 - - - 10621 RMVar_ID_10621 Human_SNP_ID_339785046 A-to-I Human chr7 + 129229247 129229247 129229247 GCACCACCATGCCCGGCTAATTTTCTATTTTCAGTAGAGATGAAGTTTCTCCATGTTGGTCAGGC GCACCACCATGCCCGGCTAATTTTCTATTTTCGGTAGAGATGAAGTTTCTCCATGTTGGTCAGGC A G AHCYL2 Ensembl:ENSG00000158467 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1269141897 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16005973 10622 RMVar_ID_10622 Human_SNP_ID_339794173 A-to-I Human chr7 + 129267327 129267326 129267328 ATCAAGCCTTATTAGGTATTTTTTTTTGAGACAGAGTTTCACTCTTGTCGCCCAGGCTGGAGTGC ATCAAGCCTTATTAGGTATTTTTTTTTGAGAC__AGTTTCACTCTTGTCGCCCAGGCTGGAGTGC CAG C AHCYL2 Ensembl:ENSG00000158467 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1347388893 Functional Loss DEL dbSNP153 33..34 33 - - - 10623 RMVar_ID_10623 Human_SNP_ID_339821123 A-to-I Human chr7 + 129386438 129386438 129386438 TGAGCTGAGATCGTGCTACTGTGCTCCAGCCTAGGTGACAGAGTAAGACCCTGGCTCAAAAAAAA TGAGCTGAGATCGTGCTACTGTGCTCCAGCCTCGGTGACAGAGTAAGACCCTGGCTCAAAAAAAA A C AHCYL2 Ensembl:ENSG00000158467 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1164961052 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_31858,RMVar_hsa_circ_314601,RMVar_hsa_circ_316649,RMVar_hsa_circ_268170,RMVar_hsa_circ_311226,RMVar_hsa_circ_45475,RMVar_hsa_circ_248374,RMVar_hsa_circ_248373,RMVar_hsa_circ_18916,RMVar_hsa_circ_248372,RMVar_hsa_circ_300725,RMVar_hsa_circ_343713,RMVar_hsa_circ_352309,RMVar_hsa_circ_306047,RMVar_hsa_circ_296779,RMVar_hsa_circ_248376,RMVar_hsa_circ_248375 10624 RMVar_ID_10624 Human_SNP_ID_339828064 A-to-I Human chr7 + 129418631 129418631 129418631 GACTTAGGTTTTTAAAAATTACTCTGGAGGCCAGGTGTGGTGGCTCATGCCTGTAGTCCCCAGCT GACTTAGGTTTTTAAAAATTACTCTGGAGGCCGGGTGTGGTGGCTCATGCCTGTAGTCCCCAGCT A G AHCYL2 Ensembl:ENSG00000158467 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334643411 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268170,RMVar_hsa_circ_36170,RMVar_hsa_circ_15442 10625 RMVar_ID_10625 Human_SNP_ID_339828431 A-to-I Human chr7 + 129420554 129420554 129420554 CAGACTGGAGTGCAGTGGCACAATCTCAGCTCACTGCAGACTCGACTTCCTGGGCTCAAGCATTC CAGACTGGAGTGCAGTGGCACAATCTCAGCTCGCTGCAGACTCGACTTCCTGGGCTCAAGCATTC A G AHCYL2 Ensembl:ENSG00000158467 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1193423641 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268170,RMVar_hsa_circ_36170,RMVar_hsa_circ_15442 10626 RMVar_ID_10626 Human_SNP_ID_339828440 A-to-I Human chr7 + 129420592 129420592 129420592 GACTCGACTTCCTGGGCTCAAGCATTCCTCCCACCTCAGCCTCCTGAGTAGCTGAAACTACAGGC GACTCGACTTCCTGGGCTCAAGCATTCCTCCCGCCTCAGCCTCCTGAGTAGCTGAAACTACAGGC A G AHCYL2 Ensembl:ENSG00000158467 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1429452953 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268170,RMVar_hsa_circ_36170,RMVar_hsa_circ_15442 10627 RMVar_ID_10627 Human_SNP_ID_339828571 A-to-I Human chr7 + 129421193 129421193 129421193 AGAATCGCTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCTAAGATCATGCCATTGCACTGCAGCC AGAATCGCTTGAACCCAGGAGGCAGAGGTTGCGGTGAGCTAAGATCATGCCATTGCACTGCAGCC A G AHCYL2 Ensembl:ENSG00000158467 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs940777515 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268170,RMVar_hsa_circ_36170,RMVar_hsa_circ_15442 10628 RMVar_ID_10628 Human_SNP_ID_339843520 A-to-I Human chr7 + 129487235 129487235 129487235 CAGGGTTTCACCATGTTAGCCAGGCTGACCTCAAACTCCTGACCTCAGGTGATCCGCCCGCCTCC CAGGGTTTCACCATGTTAGCCAGGCTGACCTCTAACTCCTGACCTCAGGTGATCCGCCCGCCTCC A T STRIP2 Ensembl:ENSG00000128578 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1483275410 Functional Loss SNV dbSNP153 33..33 33 - - - 10629 RMVar_ID_10629 Human_SNP_ID_339868385 A-to-I Human chr7 - 129588024 129588024 129588024 CCAAAGTGCTGGGATTACAGGCGAGAGCCACCATGCCCAGCCTCCTTTAAGGGACTTCTAGCCTG CCAAAGTGCTGGGATTACAGGCGAGAGCCACCGTGCCCAGCCTCCTTTAAGGGACTTCTAGCCTG T C RF00017-4495,RF00017-4489 RNACentral:URS0000923EDC,RNACentral:URS00009982F9 SRP RNA,SRP RNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031108115 Functional Loss SNV dbSNP153 33..33 33 - - - 10630 RMVar_ID_10630 Human_SNP_ID_339875333 A-to-I Human chr7 + 129614526 129614521 129614527 AAGTTAGAGATGGGGATCTTGCTATGTTGCCTAAGCTGGCCTTGAACTCCTGGGCTCAAGGAATG AAGTTAGAGATGGGGATCTTGCTATGTT______GCTGGCCTTGAACTCCTGGGCTCAAGGAATG TGCCTAA T NRF1 Ensembl:ENSG00000106459 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1415213192 Functional Loss DEL dbSNP153 29..34 33 - - - Human_RBP_ID_24189645 10631 RMVar_ID_10631 Human_SNP_ID_339876979 A-to-I Human chr7 + 129620488 129620488 129620488 TTGGCTGACTGCAACCTCCGCCTCCCGGGTTCAAGCGATTCTTCTGCCTCAGCCTCCCAAGCAGC TTGGCTGACTGCAACCTCCGCCTCCCGGGTTCGAGCGATTCTTCTGCCTCAGCCTCCCAAGCAGC A G NRF1 Ensembl:ENSG00000106459 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005212250 Functional Loss SNV dbSNP153 33..33 33 - - - 10632 RMVar_ID_10632 Human_SNP_ID_339877597 A-to-I Human chr7 + 129622784 129622784 129622784 TTGAGACAGGATTTCACCACGTTAGCTAGGCTAGTTTTGAACTCCTGACCTCAGGTGATCCGCCC TTGAGACAGGATTTCACCACGTTAGCTAGGCTGGTTTTGAACTCCTGACCTCAGGTGATCCGCCC A G NRF1 Ensembl:ENSG00000106459 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs534536314 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3055467,Human_RBP_ID_16007997 10633 RMVar_ID_10633 Human_SNP_ID_339878791 A-to-I Human chr7 + 129627410 129627410 129627410 TTTTTTTTTCTTTTTATTTTTTTCGTAGATACAAGGTCTCACCATCTTGCCCAGGCTGGTCTCAA TTTTTTTTTCTTTTTATTTTTTTCGTAGATACGAGGTCTCACCATCTTGCCCAGGCTGGTCTCAA A G NRF1 Ensembl:ENSG00000106459 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs923343153 Functional Loss SNV dbSNP153 33..33 33 - - - 10634 RMVar_ID_10634 Human_SNP_ID_339879714 A-to-I Human chr7 + 129631332 129631332 129631332 GCCTTGATCTCCCTGACTCAAGCAGTCCTTCCACCTGAGCCTCCTGAATAGCTGGGATCACAAGC GCCTTGATCTCCCTGACTCAAGCAGTCCTTCCGCCTGAGCCTCCTGAATAGCTGGGATCACAAGC A G NRF1 Ensembl:ENSG00000106459 Protein coding intron GSE100210;GSE107867;GSE107867 HepG2 cell line;ASD brains,frontal_cortex;ASD brains,temporal_cortex - 29129909,30559470,30559470 RNA-Seq:(High) rs1173510254 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_283689,RMVar_hsa_circ_349995,RMVar_hsa_circ_356375,RMVar_hsa_circ_329930,RMVar_hsa_circ_338184,RMVar_hsa_circ_320853 10635 RMVar_ID_10635 Human_SNP_ID_339879715 A-to-I Human chr7 + 129631332 129631332 129631332 GCCTTGATCTCCCTGACTCAAGCAGTCCTTCCACCTGAGCCTCCTGAATAGCTGGGATCACAAGC GCCTTGATCTCCCTGACTCAAGCAGTCCTTCCTCCTGAGCCTCCTGAATAGCTGGGATCACAAGC A T NRF1 Ensembl:ENSG00000106459 Protein coding intron GSE100210;GSE107867;GSE107867 HepG2 cell line;ASD brains,frontal_cortex;ASD brains,temporal_cortex - 29129909,30559470,30559470 RNA-Seq:(High) rs1173510254 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_283689,RMVar_hsa_circ_349995,RMVar_hsa_circ_356375,RMVar_hsa_circ_329930,RMVar_hsa_circ_338184,RMVar_hsa_circ_320853 10636 RMVar_ID_10636 Human_SNP_ID_339879760 A-to-I Human chr7 + 129631496 129631496 129631496 CGCTATATTGCCCAGGCTGGTCTTAAATTCCTAGCTCAATCAGTTCTCCCACCTTGGCCTCCTAA CGCTATATTGCCCAGGCTGGTCTTAAATTCCTGGCTCAATCAGTTCTCCCACCTTGGCCTCCTAA A G NRF1 Ensembl:ENSG00000106459 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1008729279 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_283689,RMVar_hsa_circ_349995,RMVar_hsa_circ_356375,RMVar_hsa_circ_329930,RMVar_hsa_circ_338184,RMVar_hsa_circ_320853 10637 RMVar_ID_10637 Human_SNP_ID_339903441 A-to-I Human chr7 + 129731832 129731832 129731832 TGGGATCTCCCTTTGTTGCCCAGGCTGGTCTCAAACTCCTGGGCTCAAAATGATCCTCCCGCCTT TGGGATCTCCCTTTGTTGCCCAGGCTGGTCTCGAACTCCTGGGCTCAAAATGATCCTCCCGCCTT A G NRF1 Ensembl:ENSG00000106459 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs927653919 Functional Loss SNV dbSNP153 33..33 33 - - - 10638 RMVar_ID_10638 Human_SNP_ID_339903445 A-to-I Human chr7 + 129731881 129731881 129731881 ATGATCCTCCCGCCTTAGTCTCCCAAAGTGTTAGGATTATAGGCATGAGCCACTACACCCGGCCC ATGATCCTCCCGCCTTAGTCTCCCAAAGTGTTTGGATTATAGGCATGAGCCACTACACCCGGCCC A T NRF1 Ensembl:ENSG00000106459 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027787920 Functional Loss SNV dbSNP153 33..33 33 - - - 10639 RMVar_ID_10639 Human_SNP_ID_339904392 A-to-I Human chr7 + 129735745 129735745 129735745 TGAAACTATAAGACCACCGGGCGCGGTGGCTGACGCCTGTAATCCCAGCACTTTGGGAGGCCGAG TGAAACTATAAGACCACCGGGCGCGGTGGCTGGCGCCTGTAATCCCAGCACTTTGGGAGGCCGAG A G NRF1 Ensembl:ENSG00000106459 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs538727802 Functional Loss SNV dbSNP153 33..33 33 - - - 10640 RMVar_ID_10640 Human_SNP_ID_339931799 A-to-I Human chr7 - 129842864 129842864 129842864 AGTTTTGCTCTTGTTGCACAGGCTGCGGTGCAATGGCGCAGTCTGGGCTCACTGCAAACTCCACC AGTTTTGCTCTTGTTGCACAGGCTGCGGTGCAGTGGCGCAGTCTGGGCTCACTGCAAACTCCACC T C UBE2H Ensembl:ENSG00000186591 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1413270107 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_296224,RMVar_hsa_circ_357661 10641 RMVar_ID_10641 Human_SNP_ID_339934216 A-to-I Human chr7 - 129852755 129852755 129852755 CACCATTGCACTCCAGCCTGGGCAATAAGAGCAAAACTCCATCTCAAAAAAACAAACAAAAAAAA CACCATTGCACTCCAGCCTGGGCAATAAGAGCGAAACTCCATCTCAAAAAAACAAACAAAAAAAA T C UBE2H Ensembl:ENSG00000186591 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1272043944 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_296224,RMVar_hsa_circ_357661 10642 RMVar_ID_10642 Human_SNP_ID_339934997 A-to-I Human chr7 - 129855821 129855821 129855821 GCGATAATAGCTCACTGCAGCCTTGAGCTCCTAGGCTCGAACAGTCCTCCCATCTCAGCCTCCCC GCGATAATAGCTCACTGCAGCCTTGAGCTCCTTGGCTCGAACAGTCCTCCCATCTCAGCCTCCCC T A UBE2H Ensembl:ENSG00000186591 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049409881 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_296224,RMVar_hsa_circ_357661 10643 RMVar_ID_10643 Human_SNP_ID_339939559 A-to-I Human chr7 - 129873727 129873727 129873727 GCTGCCATAGAACTTGATGTGAGGCCGAGCGCAGTGGCTCATCCTGTAATCCCAGCATTTTGGGG GCTGCCATAGAACTTGATGTGAGGCCGAGCGCGGTGGCTCATCCTGTAATCCCAGCATTTTGGGG T C UBE2H Ensembl:ENSG00000186591 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1445516605 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_248413,RMVar_hsa_circ_296224,RMVar_hsa_circ_357661,RMVar_hsa_circ_272435 10644 RMVar_ID_10644 Human_SNP_ID_339941925 A-to-I Human chr7 - 129883790 129883790 129883790 TTGCCCAGGCTGGAGTACAGTGGTGCAATCTCAGCTCACTGCAACTTCTGCCTTCCGGATTCAAG TTGCCCAGGCTGGAGTACAGTGGTGCAATCTCGGCTCACTGCAACTTCTGCCTTCCGGATTCAAG T C UBE2H Ensembl:ENSG00000186591 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1320246480 Functional Loss SNV dbSNP153 33..33 33 - - - 10645 RMVar_ID_10645 Human_SNP_ID_339943484 A-to-I Human chr7 - 129889763 129889763 129889763 CCCAGGCTGGTCTCGGACTCCTGGCCTCAAGCAATCTTTCTGCCCTTGCTTCCCAAAGTGTTGGG CCCAGGCTGGTCTCGGACTCCTGGCCTCAAGCTATCTTTCTGCCCTTGCTTCCCAAAGTGTTGGG T A UBE2H Ensembl:ENSG00000186591 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1563035601 Functional Loss SNV dbSNP153 33..33 33 - - - 10646 RMVar_ID_10646 Human_SNP_ID_339943990 A-to-I Human chr7 - 129891346 129891345 129891346 TTAGAGATTAAGAAACAGGCTCAGATTTAGCCAGGTGCGGTGGCGCATGCCTGTAATCCCAGCTA TTAGAGATTAAGAAACAGGCTCAGATTTAGCC_GGTGCGGTGGCGCATGCCTGTAATCCCAGCTA CT C UBE2H Ensembl:ENSG00000186591 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1206920979 Functional Loss DEL dbSNP153 33..33 33 - - - 10647 RMVar_ID_10647 Human_SNP_ID_339945278 A-to-I Human chr7 - 129896254 129896254 129896254 CGGCTCACTGCAACGTCTGCCTCCTAGATTCAAGCGATTCTCCTGCCTCAGCCTCTAGAGTAGCT CGGCTCACTGCAACGTCTGCCTCCTAGATTCAGGCGATTCTCCTGCCTCAGCCTCTAGAGTAGCT T C UBE2H Ensembl:ENSG00000186591 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1230827902 Functional Loss SNV dbSNP153 33..33 33 - - - 10648 RMVar_ID_10648 Human_SNP_ID_339945354 A-to-I Human chr7 - 129896538 129896538 129896538 AGCCGGATGTGCTGATGCATGCCTGTAATCCAAGCTACTGGGGTGGGTGAGGTGGGAGGATCATT AGCCGGATGTGCTGATGCATGCCTGTAATCCAGGCTACTGGGGTGGGTGAGGTGGGAGGATCATT T C UBE2H Ensembl:ENSG00000186591 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs781090211 Functional Loss SNV dbSNP153 33..33 33 - - - 10649 RMVar_ID_10649 Human_SNP_ID_339945355 A-to-I Human chr7 - 129896543 129896543 129896543 AAATGAGCCGGATGTGCTGATGCATGCCTGTAATCCAAGCTACTGGGGTGGGTGAGGTGGGAGGA AAATGAGCCGGATGTGCTGATGCATGCCTGTATTCCAAGCTACTGGGGTGGGTGAGGTGGGAGGA T A UBE2H Ensembl:ENSG00000186591 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1055444232 Functional Loss SNV dbSNP153 33..33 33 - - - 10650 RMVar_ID_10650 Human_SNP_ID_339945385 A-to-I Human chr7 - 129896680 129896680 129896680 CAGAAAAGGGCCAGGCAAGGTGACTCACACCTATAATCCCAGCACTTTGGGAGCCTGAGGTAGAA CAGAAAAGGGCCAGGCAAGGTGACTCACACCTGTAATCCCAGCACTTTGGGAGCCTGAGGTAGAA T C UBE2H Ensembl:ENSG00000186591 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs532960055 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23315690 10651 RMVar_ID_10651 Human_SNP_ID_339947712 A-to-I Human chr7 - 129906273 129906273 129906273 TTGAACCGGGAGGTGGAGGTTGCAGTGAGCCAAGGTGGCGCCACTGCACTCCAGCCTGGGCAACA TTGAACCGGGAGGTGGAGGTTGCAGTGAGCCACGGTGGCGCCACTGCACTCCAGCCTGGGCAACA T G UBE2H Ensembl:ENSG00000186591 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1324884545 Functional Loss SNV dbSNP153 33..33 33 - - - 10652 RMVar_ID_10652 Human_SNP_ID_339949067 A-to-I Human chr7 - 129911915 129911915 129911915 TCATAGACCCGGTATGGTGGCTCATGTCTGTAATCCCAGCACTTTGGGAAGCCGAGGCAGAAGGA TCATAGACCCGGTATGGTGGCTCATGTCTGTAGTCCCAGCACTTTGGGAAGCCGAGGCAGAAGGA T C UBE2H Ensembl:ENSG00000186591 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1265778597 Functional Loss SNV dbSNP153 33..33 33 - - - 10653 RMVar_ID_10653 Human_SNP_ID_339950798 A-to-I Human chr7 - 129919066 129919065 129919067 TTTGTTTTTGTTTTTGAGACAAGGTCTTGCTCAGTTACCCAGGCTTGAGTGCAGTGACACAATCA TTTGTTTTTGTTTTTGAGACAAGGTCTTGCT__GTTACCCAGGCTTGAGTGCAGTGACACAATCA CTG C UBE2H Ensembl:ENSG00000186591 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1177245756 Functional Loss DEL dbSNP153 32..33 33 - - - 10654 RMVar_ID_10654 Human_SNP_ID_339950799 A-to-I Human chr7 - 129919066 129919066 129919066 TTTGTTTTTGTTTTTGAGACAAGGTCTTGCTCAGTTACCCAGGCTTGAGTGCAGTGACACAATCA TTTGTTTTTGTTTTTGAGACAAGGTCTTGCTCGGTTACCCAGGCTTGAGTGCAGTGACACAATCA T C UBE2H Ensembl:ENSG00000186591 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1418942095 Functional Loss SNV dbSNP153 33..33 33 - - - 10655 RMVar_ID_10655 Human_SNP_ID_339951853 A-to-I Human chr7 - 129923065 129923065 129923065 GAACCCTGTCTCTACTAAAAATACAAAAAATTAGCTGGGCTTGGTGGCGGGTGCCTGTAATCCCA GAACCCTGTCTCTACTAAAAATACAAAAAATTGGCTGGGCTTGGTGGCGGGTGCCTGTAATCCCA T C UBE2H Ensembl:ENSG00000186591 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444506835 Functional Loss SNV dbSNP153 33..33 33 - - - 10656 RMVar_ID_10656 Human_SNP_ID_339952080 A-to-I Human chr7 - 129924154 129924154 129924154 TTGCCCAGGCTGATCTCTAACTCCCAGGCTCAAGTGATCCTATTACTTTGGCCTCCTGAAGTGCT TTGCCCAGGCTGATCTCTAACTCCCAGGCTCAGGTGATCCTATTACTTTGGCCTCCTGAAGTGCT T C UBE2H Ensembl:ENSG00000186591 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971305069 Functional Loss SNV dbSNP153 33..33 33 - - - 10657 RMVar_ID_10657 Human_SNP_ID_339952081 A-to-I Human chr7 - 129924154 129924154 129924154 TTGCCCAGGCTGATCTCTAACTCCCAGGCTCAAGTGATCCTATTACTTTGGCCTCCTGAAGTGCT TTGCCCAGGCTGATCTCTAACTCCCAGGCTCACGTGATCCTATTACTTTGGCCTCCTGAAGTGCT T G UBE2H Ensembl:ENSG00000186591 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971305069 Functional Loss SNV dbSNP153 33..33 33 - - - 10658 RMVar_ID_10658 Human_SNP_ID_339955235 A-to-I Human chr7 - 129935301 129935301 129935301 TCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTCAGGCATGCACTACCACGCCCAG TCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTGGCTGGGATTCAGGCATGCACTACCACGCCCAG T C UBE2H Ensembl:ENSG00000186591 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1242032127 Functional Loss SNV dbSNP153 33..33 33 - - - 10659 RMVar_ID_10659 Human_SNP_ID_339956307 A-to-I Human chr7 - 129939050 129939050 129939050 TCATGCCTGTAATCGTAGCACTTTGGGACGCCAAGGCGGATAGATCACCTGAGGTCAGGAGTTCG TCATGCCTGTAATCGTAGCACTTTGGGACGCCGAGGCGGATAGATCACCTGAGGTCAGGAGTTCG T C UBE2H Ensembl:ENSG00000186591 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1047958286 Functional Loss SNV dbSNP153 33..33 33 - - - 10660 RMVar_ID_10660 Human_SNP_ID_339957050 A-to-I Human chr7 - 129942161 129942161 129942161 TCACCTAGGCTGGAGTGCAGTGGTGTGATCACAGCTCACTGCAGCCTCGAACTTCCGGATTCTGA TCACCTAGGCTGGAGTGCAGTGGTGTGATCACGGCTCACTGCAGCCTCGAACTTCCGGATTCTGA T C UBE2H Ensembl:ENSG00000186591 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167913106 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16010509,Human_RBP_ID_26072124 10661 RMVar_ID_10661 Human_SNP_ID_339957490 A-to-I Human chr7 - 129943819 129943819 129943819 TGGCTCTCTGCAACCTCTGCCTCCTGAGTTCAAGCGATTCTCCTGCCTCACCCTCCCGAGTAGCT TGGCTCTCTGCAACCTCTGCCTCCTGAGTTCAGGCGATTCTCCTGCCTCACCCTCCCGAGTAGCT T C UBE2H Ensembl:ENSG00000186591 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1483378070 Functional Loss SNV dbSNP153 33..33 33 - - - 10662 RMVar_ID_10662 Human_SNP_ID_339957720 A-to-I Human chr7 - 129944538 129944538 129944538 TTGGCCAGGCTGGTCTCAAATTCCTGGGCTTAAGTGATCCTCTGGCCTTGGCCTCCCAAAGTGCT TTGGCCAGGCTGGTCTCAAATTCCTGGGCTTAGGTGATCCTCTGGCCTTGGCCTCCCAAAGTGCT T C UBE2H Ensembl:ENSG00000186591 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965468587 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16010555 10663 RMVar_ID_10663 Human_SNP_ID_339958738 A-to-I Human chr7 - 129948033 129948033 129948033 CAACATGGCAAAACCCCGTATGTACTTGTACTAAAAATATAAAAAATTAGCCAGGCGTGATGGTG CAACATGGCAAAACCCCGTATGTACTTGTACTGAAAATATAAAAAATTAGCCAGGCGTGATGGTG T C UBE2H Ensembl:ENSG00000186591 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017229062 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3055885 10664 RMVar_ID_10664 Human_SNP_ID_339958739 A-to-I Human chr7 - 129948036 129948036 129948036 GGCCAACATGGCAAAACCCCGTATGTACTTGTACTAAAAATATAAAAAATTAGCCAGGCGTGATG GGCCAACATGGCAAAACCCCGTATGTACTTGTGCTAAAAATATAAAAAATTAGCCAGGCGTGATG T C UBE2H Ensembl:ENSG00000186591 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1316965818 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3055885 10665 RMVar_ID_10665 Human_SNP_ID_339980021 A-to-I Human chr7 - 130028129 130028129 130028129 GACAGAGTCTTGTTCTGTCGCCAGGCTGTAGTACAGTGGTGATCTTGGCTCACTGCAACCTCCGC GACAGAGTCTTGTTCTGTCGCCAGGCTGTAGTGCAGTGGTGATCTTGGCTCACTGCAACCTCCGC T C ZC3HC1 Ensembl:ENSG00000091732 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs758727964 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36256,RMVar_hsa_circ_115738,RMVar_hsa_circ_270587,RMVar_hsa_circ_294080,RMVar_hsa_circ_279256,RMVar_hsa_circ_248417,RMVar_hsa_circ_248418,RMVar_hsa_circ_248416,RMVar_hsa_circ_99687,RMVar_hsa_circ_328455,RMVar_hsa_circ_248420,RMVar_hsa_circ_371717,RMVar_hsa_circ_248422,RMVar_hsa_circ_248423,RMVar_hsa_circ_248424,RMVar_hsa_circ_290139,RMVar_hsa_circ_283086,RMVar_hsa_circ_248425,RMVar_hsa_circ_248426 10666 RMVar_ID_10666 Human_SNP_ID_339981181 A-to-I Human chr7 - 130032594 130032593 130032595 TCTCCCAGGCTACAGTGCAGTGGCACAATCATAGCTCACTGCAGCTTTGAATTCCTGGGCTTAAG TCTCCCAGGCTACAGTGCAGTGGCACAATCA__GCTCACTGCAGCTTTGAATTCCTGGGCTTAAG CTA C ZC3HC1 Ensembl:ENSG00000091732 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1563079267 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_17577244 RMVar_hsa_circ_115738,RMVar_hsa_circ_294080,RMVar_hsa_circ_279256,RMVar_hsa_circ_248417,RMVar_hsa_circ_248416,RMVar_hsa_circ_99687,RMVar_hsa_circ_248420,RMVar_hsa_circ_371717,RMVar_hsa_circ_248423,RMVar_hsa_circ_248424,RMVar_hsa_circ_290139,RMVar_hsa_circ_283086,RMVar_hsa_circ_248427,RMVar_hsa_circ_248425,RMVar_hsa_circ_248426,RMVar_hsa_circ_275413,RMVar_hsa_circ_287127 10667 RMVar_ID_10667 Human_SNP_ID_339981389 A-to-I Human chr7 - 130033131 130033131 130033131 CTACTCGGGAAGCTGAGGTGGCAAGATCGCGTAAGCTTGGGAGGTTAAGGCTGTGGCGAGCCATG CTACTCGGGAAGCTGAGGTGGCAAGATCGCGTGAGCTTGGGAGGTTAAGGCTGTGGCGAGCCATG T C ZC3HC1 Ensembl:ENSG00000091732 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900934079 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115738,RMVar_hsa_circ_294080,RMVar_hsa_circ_279256,RMVar_hsa_circ_248417,RMVar_hsa_circ_248416,RMVar_hsa_circ_99687,RMVar_hsa_circ_248420,RMVar_hsa_circ_371717,RMVar_hsa_circ_248423,RMVar_hsa_circ_248424,RMVar_hsa_circ_290139,RMVar_hsa_circ_283086,RMVar_hsa_circ_248427,RMVar_hsa_circ_248425,RMVar_hsa_circ_248426,RMVar_hsa_circ_275413,RMVar_hsa_circ_287127 10668 RMVar_ID_10668 Human_SNP_ID_339981906 A-to-I Human chr7 - 130035146 130035146 130035146 ACCTCAAATGATCCACTCTCCTCGGCCTCCCAAAGTGCTATGATTACAAGCGTGAACCACTGTGC ACCTCAAATGATCCACTCTCCTCGGCCTCCCAGAGTGCTATGATTACAAGCGTGAACCACTGTGC T C ZC3HC1 Ensembl:ENSG00000091732 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1252497605 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115738,RMVar_hsa_circ_294080,RMVar_hsa_circ_279256,RMVar_hsa_circ_248417,RMVar_hsa_circ_248416,RMVar_hsa_circ_99687,RMVar_hsa_circ_248420,RMVar_hsa_circ_371717,RMVar_hsa_circ_248423,RMVar_hsa_circ_248424,RMVar_hsa_circ_290139,RMVar_hsa_circ_283086,RMVar_hsa_circ_248427,RMVar_hsa_circ_248425,RMVar_hsa_circ_248426,RMVar_hsa_circ_275413,RMVar_hsa_circ_287127 10669 RMVar_ID_10669 Human_SNP_ID_339982179 A-to-I Human chr7 - 130036351 130036351 130036351 CTGCCTCAGCCTCCCAAAGTGTTATTTTTAGTAGTGACGAGGTTTCACCATTTTGGCCAGGCTGT CTGCCTCAGCCTCCCAAAGTGTTATTTTTAGTGGTGACGAGGTTTCACCATTTTGGCCAGGCTGT T C ZC3HC1 Ensembl:ENSG00000091732 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1004964704 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16010795 RMVar_hsa_circ_115738,RMVar_hsa_circ_294080,RMVar_hsa_circ_279256,RMVar_hsa_circ_248417,RMVar_hsa_circ_248416,RMVar_hsa_circ_99687,RMVar_hsa_circ_248420,RMVar_hsa_circ_371717,RMVar_hsa_circ_248423,RMVar_hsa_circ_248424,RMVar_hsa_circ_290139,RMVar_hsa_circ_283086,RMVar_hsa_circ_248427,RMVar_hsa_circ_248425,RMVar_hsa_circ_248426,RMVar_hsa_circ_275413,RMVar_hsa_circ_287127 10670 RMVar_ID_10670 Human_SNP_ID_339982949 A-to-I Human chr7 - 130039924 130039924 130039924 CATGAGGTTGGGAGTTTGAGACCAGCCTGACTAACATGGTGAAACCCCATTTCTACTAAAAATAC CATGAGGTTGGGAGTTTGAGACCAGCCTGACTGACATGGTGAAACCCCATTTCTACTAAAAATAC T C ZC3HC1 Ensembl:ENSG00000091732 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1346356634 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_279256,RMVar_hsa_circ_248416,RMVar_hsa_circ_99687,RMVar_hsa_circ_248424,RMVar_hsa_circ_283086,RMVar_hsa_circ_248431,RMVar_hsa_circ_248426,RMVar_hsa_circ_287127,RMVar_hsa_circ_124360,RMVar_hsa_circ_278769,RMVar_hsa_circ_114696,RMVar_hsa_circ_248432,RMVar_hsa_circ_248429,RMVar_hsa_circ_248430 10671 RMVar_ID_10671 Human_SNP_ID_339983452 A-to-I Human chr7 - 130041352 130041352 130041352 AAACCCCATCTCTACCAAAAAATACAAAAATTAGCTGGGTGTGGTGGCGTGCACCTGTGGTCCCA AAACCCCATCTCTACCAAAAAATACAAAAATTTGCTGGGTGTGGTGGCGTGCACCTGTGGTCCCA T A ZC3HC1 Ensembl:ENSG00000091732 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1290512996 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26072301 RMVar_hsa_circ_279256,RMVar_hsa_circ_248416,RMVar_hsa_circ_99687,RMVar_hsa_circ_248424,RMVar_hsa_circ_283086,RMVar_hsa_circ_248431,RMVar_hsa_circ_248426,RMVar_hsa_circ_287127,RMVar_hsa_circ_124360,RMVar_hsa_circ_278769,RMVar_hsa_circ_114696,RMVar_hsa_circ_248432,RMVar_hsa_circ_248429,RMVar_hsa_circ_248430,RMVar_hsa_circ_283461,RMVar_hsa_circ_248433 10672 RMVar_ID_10672 Human_SNP_ID_339983468 A-to-I Human chr7 - 130041431 130041431 130041431 TGATTCCAGCACTTTGGGAGGCCAAGGTGGGCAGATCATCTGAGTTCAGGAGTTCAAGACCAGCC TGATTCCAGCACTTTGGGAGGCCAAGGTGGGCGGATCATCTGAGTTCAGGAGTTCAAGACCAGCC T C ZC3HC1 Ensembl:ENSG00000091732 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1346308473 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_279256,RMVar_hsa_circ_248416,RMVar_hsa_circ_99687,RMVar_hsa_circ_248424,RMVar_hsa_circ_283086,RMVar_hsa_circ_248431,RMVar_hsa_circ_248426,RMVar_hsa_circ_287127,RMVar_hsa_circ_124360,RMVar_hsa_circ_278769,RMVar_hsa_circ_114696,RMVar_hsa_circ_248432,RMVar_hsa_circ_248429,RMVar_hsa_circ_248430,RMVar_hsa_circ_283461,RMVar_hsa_circ_248433 10673 RMVar_ID_10673 Human_SNP_ID_339983535 A-to-I Human chr7 - 130041708 130041708 130041708 CCTGGCCAAGATGATGAAACCCTATCTCTATTAAAAATACAAAAATTAGCTGGGTGCAGTGGCAG CCTGGCCAAGATGATGAAACCCTATCTCTATTGAAAATACAAAAATTAGCTGGGTGCAGTGGCAG T C ZC3HC1 Ensembl:ENSG00000091732 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1027779343 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_279256,RMVar_hsa_circ_248416,RMVar_hsa_circ_99687,RMVar_hsa_circ_248424,RMVar_hsa_circ_283086,RMVar_hsa_circ_248431,RMVar_hsa_circ_248426,RMVar_hsa_circ_287127,RMVar_hsa_circ_278769,RMVar_hsa_circ_114696,RMVar_hsa_circ_248432,RMVar_hsa_circ_248430,RMVar_hsa_circ_283461,RMVar_hsa_circ_248433 10674 RMVar_ID_10674 Human_SNP_ID_339983636 A-to-I Human chr7 - 130042165 130042162 130042165 TCAATTAGCTGAGACTACAGGCATGCACCACCACATCCCGCTAATTTTTTGATTTTCAATAGAGA TCAATTAGCTGAGACTACAGGCATGCACCACC___TCCCGCTAATTTTTTGATTTTCAATAGAGA ATGT A ZC3HC1 Ensembl:ENSG00000091732 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1231898756 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_279256,RMVar_hsa_circ_248416,RMVar_hsa_circ_99687,RMVar_hsa_circ_248424,RMVar_hsa_circ_283086,RMVar_hsa_circ_248431,RMVar_hsa_circ_248426,RMVar_hsa_circ_287127,RMVar_hsa_circ_278769,RMVar_hsa_circ_114696,RMVar_hsa_circ_248432,RMVar_hsa_circ_248430,RMVar_hsa_circ_283461,RMVar_hsa_circ_248433 10675 RMVar_ID_10675 Human_SNP_ID_339983664 A-to-I Human chr7 - 130042272 130042272 130042272 TTGAGACAGGGTCTCATTCTGTTGCCCAGGCTAGAGGGCAGTGGTGTGATCGTATCTTACTGTGG TTGAGACAGGGTCTCATTCTGTTGCCCAGGCTGGAGGGCAGTGGTGTGATCGTATCTTACTGTGG T C ZC3HC1 Ensembl:ENSG00000091732 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs576901089 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_279256,RMVar_hsa_circ_248416,RMVar_hsa_circ_99687,RMVar_hsa_circ_248424,RMVar_hsa_circ_283086,RMVar_hsa_circ_248431,RMVar_hsa_circ_248426,RMVar_hsa_circ_287127,RMVar_hsa_circ_278769,RMVar_hsa_circ_114696,RMVar_hsa_circ_248432,RMVar_hsa_circ_248430,RMVar_hsa_circ_283461,RMVar_hsa_circ_248433 10676 RMVar_ID_10676 Human_SNP_ID_339983882 A-to-I Human chr7 - 130043268 130043268 130043268 CTCTTCAGGTAGAATTTTTCTTTTGAGACAGAATCTTGCTGTGTTGCCCAGGCTGGAGTGCAGTG CTCTTCAGGTAGAATTTTTCTTTTGAGACAGAGTCTTGCTGTGTTGCCCAGGCTGGAGTGCAGTG T C ZC3HC1 Ensembl:ENSG00000091732 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1375529134 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_279256,RMVar_hsa_circ_248416,RMVar_hsa_circ_99687,RMVar_hsa_circ_248424,RMVar_hsa_circ_283086,RMVar_hsa_circ_248431,RMVar_hsa_circ_248426,RMVar_hsa_circ_287127,RMVar_hsa_circ_278769,RMVar_hsa_circ_114696,RMVar_hsa_circ_248432,RMVar_hsa_circ_248430,RMVar_hsa_circ_283461,RMVar_hsa_circ_248433 10677 RMVar_ID_10677 Human_SNP_ID_339984586 A-to-I Human chr7 - 130046520 130046520 130046520 TCACTGTAACCTCCACCTCCTGGGTTTAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGAGA TCACTGTAACCTCCACCTCCTGGGTTTAAGCAGTTCTCCTGCCTCAGCCTCCCAAGTAGCTGAGA T C ZC3HC1 Ensembl:ENSG00000091732 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs867807951 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_279256,RMVar_hsa_circ_248416,RMVar_hsa_circ_99687,RMVar_hsa_circ_248424,RMVar_hsa_circ_283086,RMVar_hsa_circ_53843,RMVar_hsa_circ_248431,RMVar_hsa_circ_248426,RMVar_hsa_circ_287127,RMVar_hsa_circ_278769,RMVar_hsa_circ_114696,RMVar_hsa_circ_248432,RMVar_hsa_circ_283461,RMVar_hsa_circ_248433 10678 RMVar_ID_10678 Human_SNP_ID_339984587 A-to-I Human chr7 - 130046524 130046524 130046524 TGGCTCACTGTAACCTCCACCTCCTGGGTTTAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGCT TGGCTCACTGTAACCTCCACCTCCTGGGTTTAGGCAATTCTCCTGCCTCAGCCTCCCAAGTAGCT T C ZC3HC1 Ensembl:ENSG00000091732 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1443276037 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_279256,RMVar_hsa_circ_248416,RMVar_hsa_circ_99687,RMVar_hsa_circ_248424,RMVar_hsa_circ_283086,RMVar_hsa_circ_53843,RMVar_hsa_circ_248431,RMVar_hsa_circ_248426,RMVar_hsa_circ_287127,RMVar_hsa_circ_278769,RMVar_hsa_circ_114696,RMVar_hsa_circ_248432,RMVar_hsa_circ_283461,RMVar_hsa_circ_248433 10679 RMVar_ID_10679 Human_SNP_ID_339984727 A-to-I Human chr7 - 130047136 130047136 130047136 CAACATGGTGAAACCCTGTCTCTACTAAAAATACAAAAATTAACCAGGCATGGTGGCACATGCTT CAACATGGTGAAACCCTGTCTCTACTAAAAATTCAAAAATTAACCAGGCATGGTGGCACATGCTT T A ZC3HC1 Ensembl:ENSG00000091732 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1428546968 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_279256,RMVar_hsa_circ_248416,RMVar_hsa_circ_99687,RMVar_hsa_circ_248424,RMVar_hsa_circ_283086,RMVar_hsa_circ_53843,RMVar_hsa_circ_248431,RMVar_hsa_circ_248426,RMVar_hsa_circ_287127,RMVar_hsa_circ_278769,RMVar_hsa_circ_114696,RMVar_hsa_circ_248432,RMVar_hsa_circ_283461,RMVar_hsa_circ_248433 10680 RMVar_ID_10680 Human_SNP_ID_339984736 A-to-I Human chr7 - 130047198 130047198 130047198 CAAGCACTTTGGTTTGCTGAGGCAAGTGGATTACGAGGTCAAGAGTTTGAGACCAGCCTGGCCAA CAAGCACTTTGGTTTGCTGAGGCAAGTGGATTTCGAGGTCAAGAGTTTGAGACCAGCCTGGCCAA T A ZC3HC1 Ensembl:ENSG00000091732 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1223262099 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24190234 RMVar_hsa_circ_279256,RMVar_hsa_circ_248416,RMVar_hsa_circ_99687,RMVar_hsa_circ_248424,RMVar_hsa_circ_283086,RMVar_hsa_circ_53843,RMVar_hsa_circ_248431,RMVar_hsa_circ_248426,RMVar_hsa_circ_287127,RMVar_hsa_circ_278769,RMVar_hsa_circ_114696,RMVar_hsa_circ_248432,RMVar_hsa_circ_283461,RMVar_hsa_circ_248433 10681 RMVar_ID_10681 Human_SNP_ID_339992571 A-to-I Human chr7 + 130074715 130074715 130074715 CAATGTCACTGCAACCTCTGCCTCCCAGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCTGAGTAGT CAATGTCACTGCAACCTCTGCCTCCCAGGTTCGAGCAGTTCTCCTGCCTCAGCCTCCTGAGTAGT A G KLHDC10 Ensembl:ENSG00000128607 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1353224788 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_248434,RMVar_hsa_circ_106453 10682 RMVar_ID_10682 Human_SNP_ID_339993352 A-to-I Human chr7 + 130077695 130077695 130077695 CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCACCTGCTACCACGCCCAGCTAATTTTT CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTGCAGGCACCTGCTACCACGCCCAGCTAATTTTT A G KLHDC10 Ensembl:ENSG00000128607 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1183462582 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_248434,RMVar_hsa_circ_106453 10683 RMVar_ID_10683 Human_SNP_ID_339993353 A-to-I Human chr7 + 130077695 130077695 130077695 CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCACCTGCTACCACGCCCAGCTAATTTTT CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTTCAGGCACCTGCTACCACGCCCAGCTAATTTTT A T KLHDC10 Ensembl:ENSG00000128607 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1183462582 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_248434,RMVar_hsa_circ_106453 10684 RMVar_ID_10684 Human_SNP_ID_339994043 A-to-I Human chr7 + 130080142 130080142 130080142 TTTTAATTTTTTTGTAGAGATAAGGCCTTGCTATGTTGCCTAGGCTGGTTGCAAACTCCTGGCCT TTTTAATTTTTTTGTAGAGATAAGGCCTTGCTGTGTTGCCTAGGCTGGTTGCAAACTCCTGGCCT A G KLHDC10 Ensembl:ENSG00000128607 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1002400511 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17577251,Human_RBP_ID_18960410,Human_RBP_ID_21429730 RMVar_hsa_circ_248434,RMVar_hsa_circ_106453 10685 RMVar_ID_10685 Human_SNP_ID_339994056 A-to-I Human chr7 + 130080210 130080210 130080210 GTCATCCTCTCACCTCAGCCTCCCAAAGTACTAGGATTACAGGCATGAGCCACTGTGCCTGGCCC GTCATCCTCTCACCTCAGCCTCCCAAAGTACTGGGATTACAGGCATGAGCCACTGTGCCTGGCCC A G KLHDC10 Ensembl:ENSG00000128607 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1358972839 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_248434,RMVar_hsa_circ_106453 10686 RMVar_ID_10686 Human_SNP_ID_340000680 A-to-I Human chr7 + 130109252 130109252 130109252 TTTTTTTAATTTTTTAAAATTTAATTTTTTTTAGAGATGAAGTTTTGTTCTGTCACCCAGGCTGA TTTTTTTAATTTTTTAAAATTTAATTTTTTTTGGAGATGAAGTTTTGTTCTGTCACCCAGGCTGA A G KLHDC10 Ensembl:ENSG00000128607 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs377061165 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16011403 RMVar_hsa_circ_248436,RMVar_hsa_circ_62023,RMVar_hsa_circ_248434,RMVar_hsa_circ_106453,RMVar_hsa_circ_371123,RMVar_hsa_circ_248435,RMVar_hsa_circ_307203,RMVar_hsa_circ_248437 10687 RMVar_ID_10687 Human_SNP_ID_340125280 A-to-I Human chr7 - 130628827 130628820 130628828 ATGCTCAGACTGGTCTTGAACTTCTGGCATCAAGTGATCCTCCTGCCTCGGCCTCCCAAAGTGCT ATGCTCAGACTGGTCTTGAACTTCTGGCATC________CTCCTGCCTCGGCCTCCCAAAGTGCT GGATCACTT G COPG2 Ensembl:ENSG00000158623 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1240726350 Functional Loss DEL dbSNP153 32..39 33 - - - RMVar_hsa_circ_285314,RMVar_hsa_circ_51897,RMVar_hsa_circ_42011 10688 RMVar_ID_10688 Human_SNP_ID_340133446 A-to-I Human chr7 - 130659829 130659829 130659829 TGGCTCACTGCAGCCTCCGCCTCCCGGGTTTGAGCGATTCTCCTGCCTCAGCCTCTGGAGTAGCT TGGCTCACTGCAGCCTCCGCCTCCCGGGTTTGCGCGATTCTCCTGCCTCAGCCTCTGGAGTAGCT T G COPG2 Ensembl:ENSG00000158623 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1554460416 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51897,RMVar_hsa_circ_11807,RMVar_hsa_circ_281783 10689 RMVar_ID_10689 Human_SNP_ID_340189699 A-to-I Human chr7 - 130889709 130889708 130889709 TTGTAGAGACATGCAGTCTTGCTGTGTTGCCCAGGCTGGTCTCGAACTCATGGCCTCAAGCGATC TTGTAGAGACATGCAGTCTTGCTGTGTTGCCC_GGCTGGTCTCGAACTCATGGCCTCAAGCGATC CT C AC016831.1,AC016831.6 Ensembl:ENSG00000226380,Ensembl:ENSG00000285106 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1443209045 Functional Loss DEL dbSNP153 33..33 33 - - - 10690 RMVar_ID_10690 Human_SNP_ID_340198821 A-to-I Human chr7 - 130925855 130925855 130925855 CGGCTCACTGCAGTCTCCACCTCCCAGGTTCAAGTGATTCTCATGCCTCAGCCTTCCGAGTAGCC CGGCTCACTGCAGTCTCCACCTCCCAGGTTCAGGTGATTCTCATGCCTCAGCCTTCCGAGTAGCC T C AC016831.6 Ensembl:ENSG00000285106 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1242767611 Functional Loss SNV dbSNP153 33..33 33 - - - 10691 RMVar_ID_10691 Human_SNP_ID_340200293 A-to-I Human chr7 - 130932387 130932387 130932387 TAGAGATGGGGTTTCACCATGTTGCTGGTCTCAAACTCCTGACTTCAAGTGACCTGCCCGCCTCA TAGAGATGGGGTTTCACCATGTTGCTGGTCTCCAACTCCTGACTTCAAGTGACCTGCCCGCCTCA T G AC016831.6 Ensembl:ENSG00000285106 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1326619120 Functional Loss SNV dbSNP153 33..33 33 - - - 10692 RMVar_ID_10692 Human_SNP_ID_340203106 A-to-I Human chr7 - 130944865 130944865 130944865 TCCGCCAGCTACCTCTTGTGTTTAAGAATTAAAGGAAGATGAGCTAGGAATCAAGAAATACGCAG TCCGCCAGCTACCTCTTGTGTTTAAGAATTAAGGGAAGATGAGCTAGGAATCAAGAAATACGCAG T C LINC-PINT,AC016831.6 Ensembl:ENSG00000231721,Ensembl:ENSG00000285106 lincRNA,lincRNA intron,intron GSE47997;GSE38233;GSE100210;GSE99789 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 23474544,24183664,29129909,29796672 RNA-Seq:(High) rs1381636874 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5622563,Human_RBP_ID_21430981,Human_RBP_ID_21951551 Human_Splice_Rec_923978,Human_Splice_Rec_923988,Human_Splice_Rec_923998,Human_Splice_Rec_924026,Human_Splice_Rec_924036,Human_Splice_Rec_924048,Human_Splice_Rec_924062,Human_Splice_Rec_924084,Human_Splice_Rec_924094,Human_Splice_Rec_924106,Human_Splice_Rec_924114 10693 RMVar_ID_10693 Human_SNP_ID_340203180 A-to-I Human chr7 - 130945280 130945280 130945280 ACATCTCTCAAAAGGTAACAATATGATGTTTCAGGAAATTAGAGAAGTTAAGAGACTTTGCTGTA ACATCTCTCAAAAGGTAACAATATGATGTTTCCGGAAATTAGAGAAGTTAAGAGACTTTGCTGTA T G LINC-PINT,AC016831.6 Ensembl:ENSG00000231721,Ensembl:ENSG00000285106 lincRNA,lincRNA intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1350873239 Functional Loss SNV dbSNP153 33..33 33 - - - 10694 RMVar_ID_10694 Human_SNP_ID_340205248 A-to-I Human chr7 - 130954691 130954691 130954691 CTGTGTCACCCAGGCTGAGCTGCAGTGGGGCAATCTCAGCTCACTGCAACCTCTACCTCCCAGGC CTGTGTCACCCAGGCTGAGCTGCAGTGGGGCAGTCTCAGCTCACTGCAACCTCTACCTCCCAGGC T C LINC-PINT,AC016831.6 Ensembl:ENSG00000231721,Ensembl:ENSG00000285106 lincRNA,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs956568408 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_309415,RMVar_hsa_circ_293175 10695 RMVar_ID_10695 Human_SNP_ID_340205957 A-to-I Human chr7 - 130957856 130957856 130957856 ATCCCAGCTACTTGGGAGACTGAGAAAGGAAAATTGCTTGAACCTGGGAGGCAGAGGTTGCAGTG ATCCCAGCTACTTGGGAGACTGAGAAAGGAAACTTGCTTGAACCTGGGAGGCAGAGGTTGCAGTG T G LINC-PINT,AC016831.6 Ensembl:ENSG00000231721,Ensembl:ENSG00000285106 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1221948015 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3056971 RMVar_hsa_circ_309415,RMVar_hsa_circ_293175 10696 RMVar_ID_10696 Human_SNP_ID_340205982 A-to-I Human chr7 - 130958017 130958017 130958017 GCTGGGTGTGGTGTTTCACGCCTGTAATCCCAACACTTTGGGAGTCTGAGGTGGGTGGAGCACTT GCTGGGTGTGGTGTTTCACGCCTGTAATCCCAGCACTTTGGGAGTCTGAGGTGGGTGGAGCACTT T C LINC-PINT,AC016831.6 Ensembl:ENSG00000231721,Ensembl:ENSG00000285106 lincRNA,lincRNA intron,intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1563155005 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_309415,RMVar_hsa_circ_293175 10697 RMVar_ID_10697 Human_SNP_ID_340209034 A-to-I Human chr7 - 130971442 130971442 130971442 TGACTAATTTCTTTGTATTTTTTTGTAGAGACAGGGTTTTGCCATGTTGTGCAGACTGGTCTCAA TGACTAATTTCTTTGTATTTTTTTGTAGAGACGGGGTTTTGCCATGTTGTGCAGACTGGTCTCAA T C LINC-PINT,AC016831.6 Ensembl:ENSG00000231721,Ensembl:ENSG00000285106 lincRNA,lincRNA intron,intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs902611910 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_309415,RMVar_hsa_circ_286283,RMVar_hsa_circ_293175,RMVar_hsa_circ_324639 10698 RMVar_ID_10698 Human_SNP_ID_340220385 A-to-I Human chr7 - 131020137 131020137 131020137 TTGCTCAGGCTGGAGTGCAGTGGTATGATCTCAGCTCACTGCAATCTCTGCTTCTTGGGTTCAAG TTGCTCAGGCTGGAGTGCAGTGGTATGATCTCCGCTCACTGCAATCTCTGCTTCTTGGGTTCAAG T G LINC-PINT,AC016831.6 Ensembl:ENSG00000231721,Ensembl:ENSG00000285106 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1292509325 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 10699 RMVar_ID_10699 Human_SNP_ID_340225844 A-to-I Human chr7 - 131041736 131041736 131041736 GGCATGCGCCACCACACTCGGCTAATTTTGGTATTTTTAGTAGAGACGGGGTTTCACATGTTGAC GGCATGCGCCACCACACTCGGCTAATTTTGGTGTTTTTAGTAGAGACGGGGTTTCACATGTTGAC T C LINC-PINT,AC016831.6 Ensembl:ENSG00000231721,Ensembl:ENSG00000285106 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs930707361 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 10700 RMVar_ID_10700 Human_SNP_ID_340229648 A-to-I Human chr7 - 131057095 131057095 131057095 GAAAGGAGTTGAGGCCTGGTGCAGTGGCTCATACCTTTGGTCCCATTACTTTGGGAGGCTGAGGC GAAAGGAGTTGAGGCCTGGTGCAGTGGCTCATGCCTTTGGTCCCATTACTTTGGGAGGCTGAGGC T C LINC-PINT,AC016831.6 Ensembl:ENSG00000231721,Ensembl:ENSG00000285106 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1346442400 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32739,RMVar_hsa_circ_72221,RMVar_hsa_circ_248504,RMVar_hsa_circ_347577,RMVar_hsa_circ_248507 10701 RMVar_ID_10701 Human_SNP_ID_340235923 A-to-I Human chr7 - 131080502 131080502 131080502 TGGACCCAGCTACTCAGGAGGCTGAGGTGGGAAGATCGCTTGGGCCCGGGGGGTCGAGGCTGCAG TGGACCCAGCTACTCAGGAGGCTGAGGTGGGAGGATCGCTTGGGCCCGGGGGGTCGAGGCTGCAG T C LINC-PINT,AC016831.6 Ensembl:ENSG00000231721,Ensembl:ENSG00000285106 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1250318285 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32739,RMVar_hsa_circ_72221,RMVar_hsa_circ_347577,RMVar_hsa_circ_248507 10702 RMVar_ID_10702 Human_SNP_ID_340235955 A-to-I Human chr7 - 131080659 131080659 131080659 TTAAAGATCTAGGGCCAGGTGCGGTGACTTACACCTGTAATCCCAGCACTTTGGGAGGCTGAGAG TTAAAGATCTAGGGCCAGGTGCGGTGACTTACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGAG T C LINC-PINT,AC016831.6 Ensembl:ENSG00000231721,Ensembl:ENSG00000285106 lincRNA,lincRNA intron,intron GSE100210;GSE107867 HepG2 cell line;ASD brains,frontal_cortex - 29129909,30559470 RNA-Seq:(High) rs1258098140 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32739,RMVar_hsa_circ_72221,RMVar_hsa_circ_347577,RMVar_hsa_circ_248507 10703 RMVar_ID_10703 Human_SNP_ID_340238268 A-to-I Human chr7 - 131091235 131091235 131091235 GGTTGAGGATGCACCCCCGAAAAAGAAACACAAGTCACAGGAGGACCTGTGTCTTGTGCTTTTTC GGTTGAGGATGCACCCCCGAAAAAGAAACACAGGTCACAGGAGGACCTGTGTCTTGTGCTTTTTC T C LINC-PINT,AC016831.6 Ensembl:ENSG00000231721,Ensembl:ENSG00000285106 lincRNA,lincRNA intron,intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs549858057 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32739,RMVar_hsa_circ_72221,RMVar_hsa_circ_347577,RMVar_hsa_circ_248507 10704 RMVar_ID_10704 Human_SNP_ID_340238758 A-to-I Human chr7 - 131093526 131093526 131093526 TTTATATTTTTAGTAAAGACGGGGTTTCACCAAGTTGGCCAGGCTGGTCTCTCGAACTTCTAACC TTTATATTTTTAGTAAAGACGGGGTTTCACCATGTTGGCCAGGCTGGTCTCTCGAACTTCTAACC T A LINC-PINT,AC016831.6 Ensembl:ENSG00000231721,Ensembl:ENSG00000285106 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1159340874 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32739,RMVar_hsa_circ_72221,RMVar_hsa_circ_347577,RMVar_hsa_circ_248507 10705 RMVar_ID_10705 Human_SNP_ID_340238873 A-to-I Human chr7 - 131093926 131093926 131093926 GGAATGCAGTGGGATAACCCTGGTTTACTGCAACCTCCACCTCCTGGGTTCAAGCAATTCTTCTG GGAATGCAGTGGGATAACCCTGGTTTACTGCAGCCTCCACCTCCTGGGTTCAAGCAATTCTTCTG T C LINC-PINT,AC016831.6 Ensembl:ENSG00000231721,Ensembl:ENSG00000285106 lincRNA,lincRNA intron,intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1165458580 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32739,RMVar_hsa_circ_72221,RMVar_hsa_circ_347577,RMVar_hsa_circ_248507 10706 RMVar_ID_10706 Human_SNP_ID_340240332 A-to-I Human chr7 - 131100617 131100617 131100617 CTTACTGCAGCCTTAACCTCCTGGCCTCAAGCAATCTTCCCACCTCAGCCTCCCCAGGAGCTGGT CTTACTGCAGCCTTAACCTCCTGGCCTCAAGCTATCTTCCCACCTCAGCCTCCCCAGGAGCTGGT T A LINC-PINT,AC016831.6 Ensembl:ENSG00000231721,Ensembl:ENSG00000285106 lincRNA,lincRNA intron,intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs912688030 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32739,RMVar_hsa_circ_72221,RMVar_hsa_circ_347577,RMVar_hsa_circ_248507 10707 RMVar_ID_10707 Human_SNP_ID_340258113 A-to-I Human chr7 + 131173598 131173598 131173598 AAAATTAGCCTGGCGTGGTCATGCATGCCTGCAATTCCAGCTACTCAGGAGGCTGAGGCAGGAGA AAAATTAGCCTGGCGTGGTCATGCATGCCTGCTATTCCAGCTACTCAGGAGGCTGAGGCAGGAGA A T MKLN1 Ensembl:ENSG00000128585 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs756628270 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91321,RMVar_hsa_circ_114367,RMVar_hsa_circ_248512,RMVar_hsa_circ_110889,RMVar_hsa_circ_248511,RMVar_hsa_circ_328435,RMVar_hsa_circ_248513 10708 RMVar_ID_10708 Human_SNP_ID_340266450 A-to-I Human chr7 + 131206756 131206756 131206756 TTTGTTTATTTTTTTAGAGATGGGGTCTTGCTATGTTTTCCCGGCTGGTCTCAAACTCCTGGCCT TTTGTTTATTTTTTTAGAGATGGGGTCTTGCTGTGTTTTCCCGGCTGGTCTCAAACTCCTGGCCT A G MKLN1 Ensembl:ENSG00000128585 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs975138707 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91321,RMVar_hsa_circ_114367,RMVar_hsa_circ_248512,RMVar_hsa_circ_110889,RMVar_hsa_circ_248511,RMVar_hsa_circ_248513 10709 RMVar_ID_10709 Human_SNP_ID_340275024 A-to-I Human chr7 + 131242927 131242927 131242927 AGAGACCCTACTCTTAAACACAAGGCCCGATGAGAGGCCAAGGTCAAGTTTGAAGAGAGATACAA AGAGACCCTACTCTTAAACACAAGGCCCGATGGGAGGCCAAGGTCAAGTTTGAAGAGAGATACAA A G MKLN1,AC009362.1 Ensembl:ENSG00000128585,Ensembl:ENSG00000233287 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1044835896 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_675249,Human_RBP_ID_2035268,Human_RBP_ID_4925192,Human_RBP_ID_8658204,Human_RBP_ID_17587023,Human_RBP_ID_18109370,Human_RBP_ID_26543573 Human_miRNA_ID_1841050 RMVar_hsa_circ_91321,RMVar_hsa_circ_114367,RMVar_hsa_circ_248512,RMVar_hsa_circ_110889,RMVar_hsa_circ_248511,RMVar_hsa_circ_248513 10710 RMVar_ID_10710 Human_SNP_ID_340279555 A-to-I Human chr7 + 131262319 131262319 131262319 ATTAGCTGGTCGTGGTGGCGTGCGACTGTAGTACCAGCTACTTGGGAGGCTGAGGCAGGAGAATG ATTAGCTGGTCGTGGTGGCGTGCGACTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATG A C MKLN1 Ensembl:ENSG00000128585 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1230924663 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91321,RMVar_hsa_circ_114367,RMVar_hsa_circ_248512,RMVar_hsa_circ_110889,RMVar_hsa_circ_248511,RMVar_hsa_circ_248513 10711 RMVar_ID_10711 Human_SNP_ID_340279556 A-to-I Human chr7 + 131262326 131262326 131262326 GGTCGTGGTGGCGTGCGACTGTAGTACCAGCTACTTGGGAGGCTGAGGCAGGAGAATGGCTTGAA GGTCGTGGTGGCGTGCGACTGTAGTACCAGCTGCTTGGGAGGCTGAGGCAGGAGAATGGCTTGAA A G MKLN1 Ensembl:ENSG00000128585 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1271920115 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91321,RMVar_hsa_circ_114367,RMVar_hsa_circ_248512,RMVar_hsa_circ_110889,RMVar_hsa_circ_248511,RMVar_hsa_circ_248513 10712 RMVar_ID_10712 Human_SNP_ID_340298787 A-to-I Human chr7 + 131345629 131345629 131345629 CTAGCTACTTGAGAGGCTGAGGCTTGAGGATCACTTGAGCCCAGGAATTCGAGGCTGCAGTGAGC CTAGCTACTTGAGAGGCTGAGGCTTGAGGATCGCTTGAGCCCAGGAATTCGAGGCTGCAGTGAGC A G MKLN1 Ensembl:ENSG00000128585 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1490506281 Functional Loss SNV dbSNP153 33..33 33 - - - 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 10713 RMVar_ID_10713 Human_SNP_ID_340298964 A-to-I Human chr7 + 131346401 131346401 131346401 AAAGTTAGCTGGGCGTGATGGTGCACACCTGTAATCCCAGCTAGTCGGGAGGCTGAGGCAGGAGA AAAGTTAGCTGGGCGTGATGGTGCACACCTGTCATCCCAGCTAGTCGGGAGGCTGAGGCAGGAGA A C MKLN1 Ensembl:ENSG00000128585 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1468939685 Functional Loss SNV dbSNP153 33..33 33 - - - 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 10714 RMVar_ID_10714 Human_SNP_ID_340306509 A-to-I Human chr7 + 131378175 131378175 131378175 CTCTTGTCATCCAGGCTGGAGTGCAGTGGCGTAATCTTGGCTCACTGCAGCCTCCACCTCCTGGG CTCTTGTCATCCAGGCTGGAGTGCAGTGGCGTGATCTTGGCTCACTGCAGCCTCCACCTCCTGGG A G MKLN1 Ensembl:ENSG00000128585 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1169532685 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_596,RMVar_hsa_circ_91321,RMVar_hsa_circ_114367,RMVar_hsa_circ_248512,RMVar_hsa_circ_110889,RMVar_hsa_circ_248511,RMVar_hsa_circ_319018,RMVar_hsa_circ_248515,RMVar_hsa_circ_126807,RMVar_hsa_circ_248513,RMVar_hsa_circ_110362,RMVar_hsa_circ_368252,RMVar_hsa_circ_82728,RMVar_hsa_circ_248514,RMVar_hsa_circ_248518,RMVar_hsa_circ_371661,RMVar_hsa_circ_347651,RMVar_hsa_circ_365577,RMVar_hsa_circ_331689,RMVar_hsa_circ_288635,RMVar_hsa_circ_298980,RMVar_hsa_circ_303813,RMVar_hsa_circ_289669,RMVar_hsa_circ_273624,RMVar_hsa_circ_284612,RMVar_hsa_circ_248520,RMVar_hsa_circ_248522,RMVar_hsa_circ_248524,RMVar_hsa_circ_248525,RMVar_hsa_circ_248526,RMVar_hsa_circ_248523,RMVar_hsa_circ_248521 10715 RMVar_ID_10715 Human_SNP_ID_340306565 A-to-I Human chr7 + 131378372 131378372 131378372 GACCTCAGGTGATCCGCCCACCTTGGCCACCCAAAGTGCTGGGCTTACAGGCGTGAACCATCATG GACCTCAGGTGATCCGCCCACCTTGGCCACCCGAAGTGCTGGGCTTACAGGCGTGAACCATCATG A G MKLN1 Ensembl:ENSG00000128585 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1018170894 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_596,RMVar_hsa_circ_91321,RMVar_hsa_circ_114367,RMVar_hsa_circ_248512,RMVar_hsa_circ_110889,RMVar_hsa_circ_248511,RMVar_hsa_circ_319018,RMVar_hsa_circ_248515,RMVar_hsa_circ_126807,RMVar_hsa_circ_248513,RMVar_hsa_circ_110362,RMVar_hsa_circ_368252,RMVar_hsa_circ_82728,RMVar_hsa_circ_248514,RMVar_hsa_circ_248518,RMVar_hsa_circ_371661,RMVar_hsa_circ_347651,RMVar_hsa_circ_365577,RMVar_hsa_circ_331689,RMVar_hsa_circ_288635,RMVar_hsa_circ_298980,RMVar_hsa_circ_303813,RMVar_hsa_circ_289669,RMVar_hsa_circ_273624,RMVar_hsa_circ_284612,RMVar_hsa_circ_248520,RMVar_hsa_circ_248522,RMVar_hsa_circ_248524,RMVar_hsa_circ_248525,RMVar_hsa_circ_248526,RMVar_hsa_circ_248523,RMVar_hsa_circ_248521 10716 RMVar_ID_10716 Human_SNP_ID_340310041 A-to-I Human chr7 + 131393764 131393764 131393764 TCCTTCATCTGGCCTCCCAAGTAGCCAGGACTACAGGCACATACTATCATGCCCAGCTGATTTTT TCCTTCATCTGGCCTCCCAAGTAGCCAGGACTTCAGGCACATACTATCATGCCCAGCTGATTTTT A T MKLN1 Ensembl:ENSG00000128585 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs976918899 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_596,RMVar_hsa_circ_91321,RMVar_hsa_circ_114367,RMVar_hsa_circ_248512,RMVar_hsa_circ_110889,RMVar_hsa_circ_248511,RMVar_hsa_circ_319018,RMVar_hsa_circ_248515,RMVar_hsa_circ_126807,RMVar_hsa_circ_248513,RMVar_hsa_circ_110362,RMVar_hsa_circ_368252,RMVar_hsa_circ_82728,RMVar_hsa_circ_248514,RMVar_hsa_circ_248518,RMVar_hsa_circ_347651,RMVar_hsa_circ_365577,RMVar_hsa_circ_331689,RMVar_hsa_circ_288635,RMVar_hsa_circ_298980,RMVar_hsa_circ_303813,RMVar_hsa_circ_273624,RMVar_hsa_circ_284612,RMVar_hsa_circ_62622,RMVar_hsa_circ_248522,RMVar_hsa_circ_248524,RMVar_hsa_circ_248525,RMVar_hsa_circ_248526,RMVar_hsa_circ_248523,RMVar_hsa_circ_277771,RMVar_hsa_circ_285702,RMVar_hsa_circ_308719,RMVar_hsa_circ_343168,RMVar_hsa_circ_327209,RMVar_hsa_circ_295320,RMVar_hsa_circ_110742,RMVar_hsa_circ_272014,RMVar_hsa_circ_71912,RMVar_hsa_circ_248527,RMVar_hsa_circ_248531,RMVar_hsa_circ_248533,RMVar_hsa_circ_51462,RMVar_hsa_circ_248534,RMVar_hsa_circ_248532,RMVar_hsa_circ_248529,RMVar_hsa_circ_248530,RMVar_hsa_circ_248528,RMVar_hsa_circ_248536,RMVar_hsa_circ_12446,RMVar_hsa_circ_116668,RMVar_hsa_circ_376009,RMVar_hsa_circ_248537 10717 RMVar_ID_10717 Human_SNP_ID_340315394 A-to-I Human chr7 + 131416791 131416791 131416791 ATCCCTTGATCCCACAAGTTCAAGACCAGCCTAGGCAGCATAGTGAGACCCCCATCTCTATAAGA ATCCCTTGATCCCACAAGTTCAAGACCAGCCTGGGCAGCATAGTGAGACCCCCATCTCTATAAGA A G MKLN1 Ensembl:ENSG00000128585 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1016460698 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23072365 RMVar_hsa_circ_596,RMVar_hsa_circ_114367,RMVar_hsa_circ_248512,RMVar_hsa_circ_319018,RMVar_hsa_circ_126807,RMVar_hsa_circ_368252,RMVar_hsa_circ_248514,RMVar_hsa_circ_347651,RMVar_hsa_circ_365577,RMVar_hsa_circ_298980,RMVar_hsa_circ_303813,RMVar_hsa_circ_13998,RMVar_hsa_circ_62622,RMVar_hsa_circ_248525,RMVar_hsa_circ_248526,RMVar_hsa_circ_285702,RMVar_hsa_circ_343168,RMVar_hsa_circ_295320,RMVar_hsa_circ_110742,RMVar_hsa_circ_71912,RMVar_hsa_circ_17649,RMVar_hsa_circ_248527,RMVar_hsa_circ_51462,RMVar_hsa_circ_248529,RMVar_hsa_circ_248530,RMVar_hsa_circ_248528,RMVar_hsa_circ_12446,RMVar_hsa_circ_120803,RMVar_hsa_circ_33321,RMVar_hsa_circ_60460,RMVar_hsa_circ_248541,RMVar_hsa_circ_268832,RMVar_hsa_circ_34192,RMVar_hsa_circ_280059,RMVar_hsa_circ_322679,RMVar_hsa_circ_353415,RMVar_hsa_circ_37773,RMVar_hsa_circ_248542,RMVar_hsa_circ_27891,RMVar_hsa_circ_277531,RMVar_hsa_circ_349320,RMVar_hsa_circ_370623,RMVar_hsa_circ_64955,RMVar_hsa_circ_248543 10718 RMVar_ID_10718 Human_SNP_ID_340315421 A-to-I Human chr7 + 131416891 131416891 131416891 TGTAGTCTCAGCTACTCGAGAGGCTGAGTCAGAAGGATTGCTTGAGCCCAGGATTGGAGGCTACA TGTAGTCTCAGCTACTCGAGAGGCTGAGTCAGGAGGATTGCTTGAGCCCAGGATTGGAGGCTACA A G MKLN1 Ensembl:ENSG00000128585 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1176605256 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16015305 RMVar_hsa_circ_596,RMVar_hsa_circ_114367,RMVar_hsa_circ_248512,RMVar_hsa_circ_319018,RMVar_hsa_circ_126807,RMVar_hsa_circ_368252,RMVar_hsa_circ_248514,RMVar_hsa_circ_347651,RMVar_hsa_circ_365577,RMVar_hsa_circ_298980,RMVar_hsa_circ_303813,RMVar_hsa_circ_13998,RMVar_hsa_circ_62622,RMVar_hsa_circ_248525,RMVar_hsa_circ_248526,RMVar_hsa_circ_285702,RMVar_hsa_circ_343168,RMVar_hsa_circ_295320,RMVar_hsa_circ_110742,RMVar_hsa_circ_71912,RMVar_hsa_circ_17649,RMVar_hsa_circ_248527,RMVar_hsa_circ_51462,RMVar_hsa_circ_248529,RMVar_hsa_circ_248530,RMVar_hsa_circ_248528,RMVar_hsa_circ_12446,RMVar_hsa_circ_120803,RMVar_hsa_circ_33321,RMVar_hsa_circ_60460,RMVar_hsa_circ_248541,RMVar_hsa_circ_268832,RMVar_hsa_circ_34192,RMVar_hsa_circ_280059,RMVar_hsa_circ_322679,RMVar_hsa_circ_353415,RMVar_hsa_circ_37773,RMVar_hsa_circ_248542,RMVar_hsa_circ_27891,RMVar_hsa_circ_277531,RMVar_hsa_circ_349320,RMVar_hsa_circ_370623,RMVar_hsa_circ_64955,RMVar_hsa_circ_248543 10719 RMVar_ID_10719 Human_SNP_ID_340316792 A-to-I Human chr7 + 131422321 131422321 131422321 TATAATCCCAGAGTTTTGGGATGCTGAGGTGGAAGGATCACTTGAGGCTGGGAGTTCGAGATCAG TATAATCCCAGAGTTTTGGGATGCTGAGGTGGCAGGATCACTTGAGGCTGGGAGTTCGAGATCAG A C MKLN1 Ensembl:ENSG00000128585 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909307398 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16015549 RMVar_hsa_circ_596,RMVar_hsa_circ_114367,RMVar_hsa_circ_248512,RMVar_hsa_circ_319018,RMVar_hsa_circ_126807,RMVar_hsa_circ_368252,RMVar_hsa_circ_248514,RMVar_hsa_circ_347651,RMVar_hsa_circ_365577,RMVar_hsa_circ_298980,RMVar_hsa_circ_303813,RMVar_hsa_circ_13998,RMVar_hsa_circ_62622,RMVar_hsa_circ_248525,RMVar_hsa_circ_248526,RMVar_hsa_circ_285702,RMVar_hsa_circ_343168,RMVar_hsa_circ_295320,RMVar_hsa_circ_110742,RMVar_hsa_circ_71912,RMVar_hsa_circ_17649,RMVar_hsa_circ_248527,RMVar_hsa_circ_51462,RMVar_hsa_circ_248529,RMVar_hsa_circ_248530,RMVar_hsa_circ_248528,RMVar_hsa_circ_12446,RMVar_hsa_circ_120803,RMVar_hsa_circ_33321,RMVar_hsa_circ_60460,RMVar_hsa_circ_248541,RMVar_hsa_circ_268832,RMVar_hsa_circ_34192,RMVar_hsa_circ_280059,RMVar_hsa_circ_322679,RMVar_hsa_circ_353415,RMVar_hsa_circ_37773,RMVar_hsa_circ_248542,RMVar_hsa_circ_27891,RMVar_hsa_circ_277531,RMVar_hsa_circ_349320,RMVar_hsa_circ_370623,RMVar_hsa_circ_64955,RMVar_hsa_circ_248543 10720 RMVar_ID_10720 Human_SNP_ID_340316834 A-to-I Human chr7 + 131422503 131422503 131422503 TTGAGCCCAGAAGTTCGAGGCTGCAGTGAGCTATGATTGTGCCACTGCACTCCAGTCCAGTCGAC TTGAGCCCAGAAGTTCGAGGCTGCAGTGAGCTGTGATTGTGCCACTGCACTCCAGTCCAGTCGAC A G MKLN1 Ensembl:ENSG00000128585 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs983448965 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_596,RMVar_hsa_circ_114367,RMVar_hsa_circ_248512,RMVar_hsa_circ_319018,RMVar_hsa_circ_126807,RMVar_hsa_circ_368252,RMVar_hsa_circ_248514,RMVar_hsa_circ_347651,RMVar_hsa_circ_365577,RMVar_hsa_circ_298980,RMVar_hsa_circ_303813,RMVar_hsa_circ_13998,RMVar_hsa_circ_62622,RMVar_hsa_circ_248525,RMVar_hsa_circ_248526,RMVar_hsa_circ_285702,RMVar_hsa_circ_343168,RMVar_hsa_circ_295320,RMVar_hsa_circ_110742,RMVar_hsa_circ_71912,RMVar_hsa_circ_17649,RMVar_hsa_circ_248527,RMVar_hsa_circ_51462,RMVar_hsa_circ_248529,RMVar_hsa_circ_248530,RMVar_hsa_circ_248528,RMVar_hsa_circ_12446,RMVar_hsa_circ_120803,RMVar_hsa_circ_33321,RMVar_hsa_circ_60460,RMVar_hsa_circ_248541,RMVar_hsa_circ_268832,RMVar_hsa_circ_34192,RMVar_hsa_circ_280059,RMVar_hsa_circ_322679,RMVar_hsa_circ_353415,RMVar_hsa_circ_37773,RMVar_hsa_circ_248542,RMVar_hsa_circ_27891,RMVar_hsa_circ_277531,RMVar_hsa_circ_349320,RMVar_hsa_circ_370623,RMVar_hsa_circ_64955,RMVar_hsa_circ_248543 10721 RMVar_ID_10721 Human_SNP_ID_340317975 A-to-I Human chr7 + 131427756 131427756 131427756 TTTTGTATTTTTAGTAGAGACGGAGTTTCACTATGTTGGCCAGGCTGGTCTCAAACACCTGACCT TTTTGTATTTTTAGTAGAGACGGAGTTTCACTCTGTTGGCCAGGCTGGTCTCAAACACCTGACCT A C MKLN1 Ensembl:ENSG00000128585 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs532861419 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_596,RMVar_hsa_circ_114367,RMVar_hsa_circ_248512,RMVar_hsa_circ_319018,RMVar_hsa_circ_126807,RMVar_hsa_circ_368252,RMVar_hsa_circ_248514,RMVar_hsa_circ_347651,RMVar_hsa_circ_365577,RMVar_hsa_circ_298980,RMVar_hsa_circ_303813,RMVar_hsa_circ_13998,RMVar_hsa_circ_62622,RMVar_hsa_circ_248525,RMVar_hsa_circ_248526,RMVar_hsa_circ_285702,RMVar_hsa_circ_343168,RMVar_hsa_circ_295320,RMVar_hsa_circ_110742,RMVar_hsa_circ_71912,RMVar_hsa_circ_17649,RMVar_hsa_circ_248527,RMVar_hsa_circ_51462,RMVar_hsa_circ_248529,RMVar_hsa_circ_248530,RMVar_hsa_circ_248528,RMVar_hsa_circ_12446,RMVar_hsa_circ_120803,RMVar_hsa_circ_33321,RMVar_hsa_circ_60460,RMVar_hsa_circ_248541,RMVar_hsa_circ_268832,RMVar_hsa_circ_34192,RMVar_hsa_circ_280059,RMVar_hsa_circ_322679,RMVar_hsa_circ_353415,RMVar_hsa_circ_37773,RMVar_hsa_circ_248542,RMVar_hsa_circ_27891,RMVar_hsa_circ_277531,RMVar_hsa_circ_349320,RMVar_hsa_circ_370623,RMVar_hsa_circ_64955,RMVar_hsa_circ_248543 10722 RMVar_ID_10722 Human_SNP_ID_340317976 A-to-I Human chr7 + 131427756 131427756 131427756 TTTTGTATTTTTAGTAGAGACGGAGTTTCACTATGTTGGCCAGGCTGGTCTCAAACACCTGACCT TTTTGTATTTTTAGTAGAGACGGAGTTTCACTGTGTTGGCCAGGCTGGTCTCAAACACCTGACCT A G MKLN1 Ensembl:ENSG00000128585 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs532861419 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_596,RMVar_hsa_circ_114367,RMVar_hsa_circ_248512,RMVar_hsa_circ_319018,RMVar_hsa_circ_126807,RMVar_hsa_circ_368252,RMVar_hsa_circ_248514,RMVar_hsa_circ_347651,RMVar_hsa_circ_365577,RMVar_hsa_circ_298980,RMVar_hsa_circ_303813,RMVar_hsa_circ_13998,RMVar_hsa_circ_62622,RMVar_hsa_circ_248525,RMVar_hsa_circ_248526,RMVar_hsa_circ_285702,RMVar_hsa_circ_343168,RMVar_hsa_circ_295320,RMVar_hsa_circ_110742,RMVar_hsa_circ_71912,RMVar_hsa_circ_17649,RMVar_hsa_circ_248527,RMVar_hsa_circ_51462,RMVar_hsa_circ_248529,RMVar_hsa_circ_248530,RMVar_hsa_circ_248528,RMVar_hsa_circ_12446,RMVar_hsa_circ_120803,RMVar_hsa_circ_33321,RMVar_hsa_circ_60460,RMVar_hsa_circ_248541,RMVar_hsa_circ_268832,RMVar_hsa_circ_34192,RMVar_hsa_circ_280059,RMVar_hsa_circ_322679,RMVar_hsa_circ_353415,RMVar_hsa_circ_37773,RMVar_hsa_circ_248542,RMVar_hsa_circ_27891,RMVar_hsa_circ_277531,RMVar_hsa_circ_349320,RMVar_hsa_circ_370623,RMVar_hsa_circ_64955,RMVar_hsa_circ_248543 10723 RMVar_ID_10723 Human_SNP_ID_340318010 A-to-I Human chr7 + 131427906 131427906 131427906 GAAGAAGGGGCTGAATGGGGTGGCTCATGCCTATAATCCTGGTACTTTGGGAGGCTGAGGTGGGA GAAGAAGGGGCTGAATGGGGTGGCTCATGCCTGTAATCCTGGTACTTTGGGAGGCTGAGGTGGGA A G MKLN1 Ensembl:ENSG00000128585 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1309738597 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17577585 RMVar_hsa_circ_596,RMVar_hsa_circ_114367,RMVar_hsa_circ_248512,RMVar_hsa_circ_319018,RMVar_hsa_circ_126807,RMVar_hsa_circ_368252,RMVar_hsa_circ_248514,RMVar_hsa_circ_347651,RMVar_hsa_circ_365577,RMVar_hsa_circ_298980,RMVar_hsa_circ_303813,RMVar_hsa_circ_13998,RMVar_hsa_circ_62622,RMVar_hsa_circ_248525,RMVar_hsa_circ_248526,RMVar_hsa_circ_285702,RMVar_hsa_circ_343168,RMVar_hsa_circ_295320,RMVar_hsa_circ_110742,RMVar_hsa_circ_71912,RMVar_hsa_circ_17649,RMVar_hsa_circ_248527,RMVar_hsa_circ_51462,RMVar_hsa_circ_248529,RMVar_hsa_circ_248530,RMVar_hsa_circ_248528,RMVar_hsa_circ_12446,RMVar_hsa_circ_120803,RMVar_hsa_circ_33321,RMVar_hsa_circ_60460,RMVar_hsa_circ_248541,RMVar_hsa_circ_268832,RMVar_hsa_circ_34192,RMVar_hsa_circ_280059,RMVar_hsa_circ_322679,RMVar_hsa_circ_353415,RMVar_hsa_circ_37773,RMVar_hsa_circ_248542,RMVar_hsa_circ_27891,RMVar_hsa_circ_277531,RMVar_hsa_circ_349320,RMVar_hsa_circ_370623,RMVar_hsa_circ_64955,RMVar_hsa_circ_248543 10724 RMVar_ID_10724 Human_SNP_ID_340337823 A-to-I Human chr7 - 131510291 131510291 131510291 GTGTTTCACCATGTCAGCCAGGCTGGTCTTGAACTCCTGACCTCGGGTGATCTGCCCACCTTGGC GTGTTTCACCATGTCAGCCAGGCTGGTCTTGACCTCCTGACCTCGGGTGATCTGCCCACCTTGGC T G PODXL Ensembl:ENSG00000128567 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749162132 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_924452,Human_Splice_Rec_924453 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_248567 10725 RMVar_ID_10725 Human_SNP_ID_340337833 A-to-I Human chr7 - 131510316 131510316 131510316 TTTTTTTTTTTTTCAAGTAGAGACAGTGTTTCACCATGTCAGCCAGGCTGGTCTTGAACTCCTGA TTTTTTTTTTTTTCAAGTAGAGACAGTGTTTCCCCATGTCAGCCAGGCTGGTCTTGAACTCCTGA T G PODXL Ensembl:ENSG00000128567 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1364017072 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_924452,Human_Splice_Rec_924453 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_248567 10726 RMVar_ID_10726 Human_SNP_ID_340346198 A-to-I Human chr7 - 131543302 131543302 131543302 GGGCAACATAGTGAGGCCCTATCTCTACATACAGTTTAAAAATTAGTCAAGCATGGTGGTATGGA GGGCAACATAGTGAGGCCCTATCTCTACATACGGTTTAAAAATTAGTCAAGCATGGTGGTATGGA T C PODXL Ensembl:ENSG00000128567 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs534991623 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_248568,RMVar_hsa_circ_248566,RMVar_hsa_circ_98583,RMVar_hsa_circ_376614 10727 RMVar_ID_10727 Human_SNP_ID_340681381 A-to-I Human chr7 - 132860026 132860026 132860026 GCCCAAGCAATCTGCCTCACTGACTTCCCAAAATGCTGGGATTACAGGCGTAAGCCACCGAGCCG GCCCAAGCAATCTGCCTCACTGACTTCCCAAAGTGCTGGGATTACAGGCGTAAGCCACCGAGCCG T C CHCHD3 Ensembl:ENSG00000106554 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444526393 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_325510 10728 RMVar_ID_10728 Human_SNP_ID_340681397 A-to-I Human chr7 - 132860079 132860079 132860079 TTTTGTGTAGACATGGTTTTGCCATGTTACCTAGGCTGGTCTTGAACTCCCGGGCCCAAGCAATC TTTTGTGTAGACATGGTTTTGCCATGTTACCTCGGCTGGTCTTGAACTCCCGGGCCCAAGCAATC T G CHCHD3 Ensembl:ENSG00000106554 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs528745915 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_325510 10729 RMVar_ID_10729 Human_SNP_ID_340694501 A-to-I Human chr7 - 132916804 132916804 132916804 GGCTGAGGTGGGAGGACTGCTTGAGTCCCAGAAATTTGAGACCAGCCTGGGCAAATATAGAGAGA GGCTGAGGTGGGAGGACTGCTTGAGTCCCAGACATTTGAGACCAGCCTGGGCAAATATAGAGAGA T G CHCHD3 Ensembl:ENSG00000106554 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1395480565 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57563,RMVar_hsa_circ_325510,RMVar_hsa_circ_362372,RMVar_hsa_circ_50703 10730 RMVar_ID_10730 Human_SNP_ID_340702716 A-to-I Human chr7 - 132954966 132954966 132954966 TTCCTTGATGTTTTTGCTCAGAGAGGAAACCCATCTCTGCGGTACATGGTATGGCCTCCATTTTT TTCCTTGATGTTTTTGCTCAGAGAGGAAACCCGTCTCTGCGGTACATGGTATGGCCTCCATTTTT T C CHCHD3 Ensembl:ENSG00000106554 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs531486707 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57563,RMVar_hsa_circ_325510,RMVar_hsa_circ_362372,RMVar_hsa_circ_50703 10731 RMVar_ID_10731 Human_SNP_ID_340714805 A-to-I Human chr7 - 133006262 133006262 133006262 AGGGTTTCATCATGTTGGTCAGGCTGGTCTCTAACTCTGGACCTCAGGTGATCTGCCTGCCTTGG AGGGTTTCATCATGTTGGTCAGGCTGGTCTCTGACTCTGGACCTCAGGTGATCTGCCTGCCTTGG T C CHCHD3 Ensembl:ENSG00000106554 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs914470837 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_362372,RMVar_hsa_circ_50703,RMVar_hsa_circ_248609,RMVar_hsa_circ_290100,RMVar_hsa_circ_300564,RMVar_hsa_circ_248608 10732 RMVar_ID_10732 Human_SNP_ID_340852309 A-to-I Human chr7 + 133585522 133585511 133585522 GGTGGCGCACACCTGTGGTCCCAGTTACTCGGAAGGCTGGGTGGAAGGATCACTTGAGCCTGGAA GGTGGCGCACACCTGTGGTCCC___________AGGCTGGGTGGAAGGATCACTTGAGCCTGGAA CAGTTACTCGGA C EXOC4 Ensembl:ENSG00000131558 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971265352 Functional Loss DEL dbSNP153 23..33 33 - - - RMVar_hsa_circ_324917,RMVar_hsa_circ_295146,RMVar_hsa_circ_16444,RMVar_hsa_circ_33522,RMVar_hsa_circ_343374,RMVar_hsa_circ_348306,RMVar_hsa_circ_367446 10733 RMVar_ID_10733 Human_SNP_ID_340852316 A-to-I Human chr7 + 133585522 133585522 133585522 GGTGGCGCACACCTGTGGTCCCAGTTACTCGGAAGGCTGGGTGGAAGGATCACTTGAGCCTGGAA GGTGGCGCACACCTGTGGTCCCAGTTACTCGGGAGGCTGGGTGGAAGGATCACTTGAGCCTGGAA A G EXOC4 Ensembl:ENSG00000131558 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025293688 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_324917,RMVar_hsa_circ_295146,RMVar_hsa_circ_16444,RMVar_hsa_circ_33522,RMVar_hsa_circ_343374,RMVar_hsa_circ_348306,RMVar_hsa_circ_367446 10734 RMVar_ID_10734 Human_SNP_ID_340864080 A-to-I Human chr7 + 133634358 133634358 133634358 TTGTTTTTTCTTTACAGTCAGGCATGTCTCTTAGAGAGTAAATTTCTGGAAAGAAATGGGCTTTA TTGTTTTTTCTTTACAGTCAGGCATGTCTCTTGGAGAGTAAATTTCTGGAAAGAAATGGGCTTTA A G EXOC4 Ensembl:ENSG00000131558 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1185200239 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 10735 RMVar_ID_10735 Human_SNP_ID_340878521 A-to-I Human chr7 + 133695056 133695056 133695056 GTTGGTCAGGCTGGTCTGGAACTCCTGACCTCAGGTAATCGGCCCACCTCGGCCTCCCAAAGTGC GTTGGTCAGGCTGGTCTGGAACTCCTGACCTCGGGTAATCGGCCCACCTCGGCCTCCCAAAGTGC A G EXOC4 Ensembl:ENSG00000131558 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934240668 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26075189 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 10736 RMVar_ID_10736 Human_SNP_ID_340881065 A-to-I Human chr7 + 133705432 133705432 133705432 ATTTCTAAAATTATAAATGTACTGGAACTGCTAGTTAAATTCTGTCTGCTTCTAGTAGAAACTAT ATTTCTAAAATTATAAATGTACTGGAACTGCTGGTTAAATTCTGTCTGCTTCTAGTAGAAACTAT A G EXOC4 Ensembl:ENSG00000131558 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs112744717 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 10737 RMVar_ID_10737 Human_SNP_ID_340881080 A-to-I Human chr7 + 133705491 133705491 133705491 AACTATAGTTACTAAACAAATAAAAATATAGTAGTTCCTCCTTATCCACAATTTTGCTATCTGTG AACTATAGTTACTAAACAAATAAAAATATAGTGGTTCCTCCTTATCCACAATTTTGCTATCTGTG A G EXOC4 Ensembl:ENSG00000131558 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1356272626 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 10738 RMVar_ID_10738 Human_SNP_ID_340881089 A-to-I Human chr7 + 133705517 133705514 133705518 TATAGTAGTTCCTCCTTATCCACAATTTTGCTATCTGTGACTTCAGTTACCCATAGTCAATTGTG TATAGTAGTTCCTCCTTATCCACAATTTTG____CTGTGACTTCAGTTACCCATAGTCAATTGTG GCTAT G EXOC4 Ensembl:ENSG00000131558 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1414748150 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_17577962 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 10739 RMVar_ID_10739 Human_SNP_ID_340881090 A-to-I Human chr7 + 133705517 133705517 133705517 TATAGTAGTTCCTCCTTATCCACAATTTTGCTATCTGTGACTTCAGTTACCCATAGTCAATTGTG TATAGTAGTTCCTCCTTATCCACAATTTTGCTCTCTGTGACTTCAGTTACCCATAGTCAATTGTG A C EXOC4 Ensembl:ENSG00000131558 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs140515256 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17577962 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 10740 RMVar_ID_10740 Human_SNP_ID_340881091 A-to-I Human chr7 + 133705517 133705517 133705517 TATAGTAGTTCCTCCTTATCCACAATTTTGCTATCTGTGACTTCAGTTACCCATAGTCAATTGTG TATAGTAGTTCCTCCTTATCCACAATTTTGCTGTCTGTGACTTCAGTTACCCATAGTCAATTGTG A G EXOC4 Ensembl:ENSG00000131558 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs140515256 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17577962 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 10741 RMVar_ID_10741 Human_SNP_ID_340928872 A-to-I Human chr7 + 133900939 133900939 133900939 TTGCCCAGGCTGGAGTGCGGTGGCACGATCTCAGCTCACTGCAGCCTCCGCCTCCCAGATTCACA TTGCCCAGGCTGGAGTGCGGTGGCACGATCTCTGCTCACTGCAGCCTCCGCCTCCCAGATTCACA A T EXOC4 Ensembl:ENSG00000131558 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928631700 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16444,RMVar_hsa_circ_343374,RMVar_hsa_circ_354739,RMVar_hsa_circ_357380,RMVar_hsa_circ_272962,RMVar_hsa_circ_330267,RMVar_hsa_circ_333410,RMVar_hsa_circ_248638,RMVar_hsa_circ_291938,RMVar_hsa_circ_310174,RMVar_hsa_circ_314370,RMVar_hsa_circ_111333,RMVar_hsa_circ_248636,RMVar_hsa_circ_248637,RMVar_hsa_circ_248635 10742 RMVar_ID_10742 Human_SNP_ID_340957321 A-to-I Human chr7 + 134020875 134020875 134020875 AGGCACGGTGGCAGGTGCCTGTAGTCCCAGCTACTTGGGAGGCTGAAGCAGGAGAATGGCGTGAA AGGCACGGTGGCAGGTGCCTGTAGTCCCAGCTGCTTGGGAGGCTGAAGCAGGAGAATGGCGTGAA A G EXOC4 Ensembl:ENSG00000131558 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1005219782 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_248638,RMVar_hsa_circ_111333 10743 RMVar_ID_10743 Human_SNP_ID_341113899 A-to-I Human chr7 + 134671787 134671786 134671788 GAATAATTTCTGGACCCTAGCAGCCAAACCATAAAAGTGTTACTTACAGTTGAATAAACATTTAC GAATAATTTCTGGACCCTAGCAGCCAAACCAT__AAGTGTTACTTACAGTTGAATAAACATTTAC TAA T BPGM Ensembl:ENSG00000172331 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006516352 Functional Loss DEL dbSNP153 33..34 33 - - - 10744 RMVar_ID_10744 Human_SNP_ID_341114032 A-to-I Human chr7 + 134672433 134672433 134672433 AGAACACAGTGCCTTGCCCATTGCAAGAATTTAGTGAATGTTTGTTCAACTGTAAGTAACACTAT AGAACACAGTGCCTTGCCCATTGCAAGAATTTCGTGAATGTTTGTTCAACTGTAAGTAACACTAT A C BPGM Ensembl:ENSG00000172331 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569190314 Functional Loss SNV dbSNP153 33..33 33 - - - 10745 RMVar_ID_10745 Human_SNP_ID_341114033 A-to-I Human chr7 + 134672433 134672433 134672433 AGAACACAGTGCCTTGCCCATTGCAAGAATTTAGTGAATGTTTGTTCAACTGTAAGTAACACTAT AGAACACAGTGCCTTGCCCATTGCAAGAATTTGGTGAATGTTTGTTCAACTGTAAGTAACACTAT A G BPGM Ensembl:ENSG00000172331 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569190314 Functional Loss SNV dbSNP153 33..33 33 - - - 10746 RMVar_ID_10746 Human_SNP_ID_640047957 A-to-I Human chr18 - 21002834 21002834 21002834 TAGGAGGCTCAGGTGGAGGATTGCTTGAGCCCAGGAGATGGAGGTTGCAGTGAGCTGAAATCGTG TAGGAGGCTCAGGTGGAGGATTGCTTGAGCCCGGGAGATGGAGGTTGCAGTGAGCTGAAATCGTG T C ROCK1 Ensembl:ENSG00000067900 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs751067162 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1207,RMVar_hsa_circ_318804,RMVar_hsa_circ_102429,RMVar_hsa_circ_188919,RMVar_hsa_circ_359843,RMVar_hsa_circ_58456,RMVar_hsa_circ_126925,RMVar_hsa_circ_59320,RMVar_hsa_circ_188922,RMVar_hsa_circ_269299,RMVar_hsa_circ_342026,RMVar_hsa_circ_188923,RMVar_hsa_circ_378677,RMVar_hsa_circ_266727,RMVar_hsa_circ_346780,RMVar_hsa_circ_188930,RMVar_hsa_circ_57538,RMVar_hsa_circ_188929,RMVar_hsa_circ_44033,RMVar_hsa_circ_73699,RMVar_hsa_circ_56530,RMVar_hsa_circ_359526,RMVar_hsa_circ_324271,RMVar_hsa_circ_62879,RMVar_hsa_circ_16108,RMVar_hsa_circ_72764,RMVar_hsa_circ_13052,RMVar_hsa_circ_188934,RMVar_hsa_circ_61748,RMVar_hsa_circ_266168,RMVar_hsa_circ_335779,RMVar_hsa_circ_345954,RMVar_hsa_circ_188939,RMVar_hsa_circ_58283,RMVar_hsa_circ_281528,RMVar_hsa_circ_329205,RMVar_hsa_circ_30329,RMVar_hsa_circ_38743,RMVar_hsa_circ_25390,RMVar_hsa_circ_24223,RMVar_hsa_circ_188943,RMVar_hsa_circ_188944,RMVar_hsa_circ_188942,RMVar_hsa_circ_69118,RMVar_hsa_circ_267257,RMVar_hsa_circ_188945 10747 RMVar_ID_10747 Human_SNP_ID_640051134 A-to-I Human chr18 - 21017824 21017824 21017824 GGACTACAGGCGCCCGCCACCATGCCTGGCTAATTTTTTGAATTCTTTAGTAGAGACGGGGTTTC GGACTACAGGCGCCCGCCACCATGCCTGGCTACTTTTTTGAATTCTTTAGTAGAGACGGGGTTTC T G ROCK1 Ensembl:ENSG00000067900 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1266268935 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1207,RMVar_hsa_circ_318804,RMVar_hsa_circ_102429,RMVar_hsa_circ_188919,RMVar_hsa_circ_359843,RMVar_hsa_circ_58456,RMVar_hsa_circ_126925,RMVar_hsa_circ_59320,RMVar_hsa_circ_188922,RMVar_hsa_circ_269299,RMVar_hsa_circ_342026,RMVar_hsa_circ_188923,RMVar_hsa_circ_378677,RMVar_hsa_circ_266727,RMVar_hsa_circ_346780,RMVar_hsa_circ_188930,RMVar_hsa_circ_188929,RMVar_hsa_circ_44033,RMVar_hsa_circ_73699,RMVar_hsa_circ_359526,RMVar_hsa_circ_111839,RMVar_hsa_circ_16108,RMVar_hsa_circ_72764,RMVar_hsa_circ_13052,RMVar_hsa_circ_61748,RMVar_hsa_circ_266168,RMVar_hsa_circ_335779,RMVar_hsa_circ_345954,RMVar_hsa_circ_188939,RMVar_hsa_circ_281528,RMVar_hsa_circ_329205,RMVar_hsa_circ_30329,RMVar_hsa_circ_38743,RMVar_hsa_circ_25390,RMVar_hsa_circ_6799,RMVar_hsa_circ_24223,RMVar_hsa_circ_188943,RMVar_hsa_circ_188944,RMVar_hsa_circ_188942,RMVar_hsa_circ_69118,RMVar_hsa_circ_368246,RMVar_hsa_circ_188945,RMVar_hsa_circ_361275,RMVar_hsa_circ_332795,RMVar_hsa_circ_275859,RMVar_hsa_circ_282481,RMVar_hsa_circ_188948,RMVar_hsa_circ_188949,RMVar_hsa_circ_188947,RMVar_hsa_circ_341519,RMVar_hsa_circ_36210,RMVar_hsa_circ_333334,RMVar_hsa_circ_188950,RMVar_hsa_circ_18133,RMVar_hsa_circ_51752,RMVar_hsa_circ_188951 10748 RMVar_ID_10748 Human_SNP_ID_640052846 A-to-I Human chr18 - 21025571 21025571 21025571 CACCATGCCTGGCTAATCTTTGTATTTTTATTAGAGATGGGGTTTTGCCATGTTGGCCAGGCTGT CACCATGCCTGGCTAATCTTTGTATTTTTATTGGAGATGGGGTTTTGCCATGTTGGCCAGGCTGT T C ROCK1 Ensembl:ENSG00000067900 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1323395176 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_318804,RMVar_hsa_circ_102429,RMVar_hsa_circ_188919,RMVar_hsa_circ_359843,RMVar_hsa_circ_126925,RMVar_hsa_circ_59320,RMVar_hsa_circ_188922,RMVar_hsa_circ_269299,RMVar_hsa_circ_342026,RMVar_hsa_circ_188923,RMVar_hsa_circ_378677,RMVar_hsa_circ_266727,RMVar_hsa_circ_346780,RMVar_hsa_circ_188930,RMVar_hsa_circ_188929,RMVar_hsa_circ_44033,RMVar_hsa_circ_73699,RMVar_hsa_circ_359526,RMVar_hsa_circ_72764,RMVar_hsa_circ_13052,RMVar_hsa_circ_61748,RMVar_hsa_circ_335779,RMVar_hsa_circ_345954,RMVar_hsa_circ_188939,RMVar_hsa_circ_329205,RMVar_hsa_circ_30329,RMVar_hsa_circ_38743,RMVar_hsa_circ_25390,RMVar_hsa_circ_6799,RMVar_hsa_circ_188944,RMVar_hsa_circ_368246,RMVar_hsa_circ_188945,RMVar_hsa_circ_332795,RMVar_hsa_circ_275859,RMVar_hsa_circ_282481,RMVar_hsa_circ_188948,RMVar_hsa_circ_188949,RMVar_hsa_circ_341519,RMVar_hsa_circ_36210,RMVar_hsa_circ_188953,RMVar_hsa_circ_18133,RMVar_hsa_circ_51752,RMVar_hsa_circ_303770,RMVar_hsa_circ_323055,RMVar_hsa_circ_313893,RMVar_hsa_circ_266142,RMVar_hsa_circ_188954,RMVar_hsa_circ_14133,RMVar_hsa_circ_290915,RMVar_hsa_circ_188956,RMVar_hsa_circ_330058,RMVar_hsa_circ_271047,RMVar_hsa_circ_188957,RMVar_hsa_circ_188958 10749 RMVar_ID_10749 Human_SNP_ID_640052849 A-to-I Human chr18 - 21025589 21025589 21025589 GGGATTACAGGTGCGTACCACCATGCCTGGCTAATCTTTGTATTTTTATTAGAGATGGGGTTTTG GGGATTACAGGTGCGTACCACCATGCCTGGCTGATCTTTGTATTTTTATTAGAGATGGGGTTTTG T C ROCK1 Ensembl:ENSG00000067900 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1242064192 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_318804,RMVar_hsa_circ_102429,RMVar_hsa_circ_188919,RMVar_hsa_circ_359843,RMVar_hsa_circ_126925,RMVar_hsa_circ_59320,RMVar_hsa_circ_188922,RMVar_hsa_circ_269299,RMVar_hsa_circ_342026,RMVar_hsa_circ_188923,RMVar_hsa_circ_378677,RMVar_hsa_circ_266727,RMVar_hsa_circ_346780,RMVar_hsa_circ_188930,RMVar_hsa_circ_188929,RMVar_hsa_circ_44033,RMVar_hsa_circ_73699,RMVar_hsa_circ_359526,RMVar_hsa_circ_72764,RMVar_hsa_circ_13052,RMVar_hsa_circ_61748,RMVar_hsa_circ_335779,RMVar_hsa_circ_345954,RMVar_hsa_circ_188939,RMVar_hsa_circ_329205,RMVar_hsa_circ_30329,RMVar_hsa_circ_38743,RMVar_hsa_circ_25390,RMVar_hsa_circ_6799,RMVar_hsa_circ_188944,RMVar_hsa_circ_368246,RMVar_hsa_circ_188945,RMVar_hsa_circ_332795,RMVar_hsa_circ_275859,RMVar_hsa_circ_282481,RMVar_hsa_circ_188948,RMVar_hsa_circ_188949,RMVar_hsa_circ_341519,RMVar_hsa_circ_36210,RMVar_hsa_circ_188953,RMVar_hsa_circ_18133,RMVar_hsa_circ_51752,RMVar_hsa_circ_303770,RMVar_hsa_circ_323055,RMVar_hsa_circ_313893,RMVar_hsa_circ_266142,RMVar_hsa_circ_188954,RMVar_hsa_circ_14133,RMVar_hsa_circ_290915,RMVar_hsa_circ_188956,RMVar_hsa_circ_330058,RMVar_hsa_circ_271047,RMVar_hsa_circ_188957,RMVar_hsa_circ_188958 10750 RMVar_ID_10750 Human_SNP_ID_640054564 A-to-I Human chr18 - 21032652 21032652 21032652 AGCCAGGCATGGTGGTGCACTCCTATAGTCCCAGCTACATCAGAGGCTGAGGCAGAGAATCACTT AGCCAGGCATGGTGGTGCACTCCTATAGTCCCGGCTACATCAGAGGCTGAGGCAGAGAATCACTT T C ROCK1 Ensembl:ENSG00000067900 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054597014 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_318804,RMVar_hsa_circ_102429,RMVar_hsa_circ_188919,RMVar_hsa_circ_359843,RMVar_hsa_circ_126925,RMVar_hsa_circ_59320,RMVar_hsa_circ_188922,RMVar_hsa_circ_269299,RMVar_hsa_circ_342026,RMVar_hsa_circ_188923,RMVar_hsa_circ_378677,RMVar_hsa_circ_266727,RMVar_hsa_circ_188930,RMVar_hsa_circ_188929,RMVar_hsa_circ_44033,RMVar_hsa_circ_73699,RMVar_hsa_circ_359526,RMVar_hsa_circ_72764,RMVar_hsa_circ_13052,RMVar_hsa_circ_61748,RMVar_hsa_circ_335779,RMVar_hsa_circ_345954,RMVar_hsa_circ_188939,RMVar_hsa_circ_329205,RMVar_hsa_circ_30329,RMVar_hsa_circ_38743,RMVar_hsa_circ_6799,RMVar_hsa_circ_188944,RMVar_hsa_circ_368246,RMVar_hsa_circ_188945,RMVar_hsa_circ_332795,RMVar_hsa_circ_275859,RMVar_hsa_circ_188949,RMVar_hsa_circ_341519,RMVar_hsa_circ_36210,RMVar_hsa_circ_6790,RMVar_hsa_circ_188953,RMVar_hsa_circ_18133,RMVar_hsa_circ_51752,RMVar_hsa_circ_303770,RMVar_hsa_circ_323055,RMVar_hsa_circ_313893,RMVar_hsa_circ_266142,RMVar_hsa_circ_188954,RMVar_hsa_circ_14133,RMVar_hsa_circ_290915,RMVar_hsa_circ_188956,RMVar_hsa_circ_330058,RMVar_hsa_circ_188958,RMVar_hsa_circ_288259,RMVar_hsa_circ_293682,RMVar_hsa_circ_369058,RMVar_hsa_circ_288150,RMVar_hsa_circ_188960,RMVar_hsa_circ_188961,RMVar_hsa_circ_188959 10751 RMVar_ID_10751 Human_SNP_ID_640113643 A-to-I Human chr18 + 21304679 21304679 21304679 GATTGGGAACCTATTCTGGAGATAGCCTTACTAGCAGATTGAATGGAGGATCTGTTTAGAGAAAG GATTGGGAACCTATTCTGGAGATAGCCTTACTGGCAGATTGAATGGAGGATCTGTTTAGAGAAAG A G GREB1L Ensembl:ENSG00000141449 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1308078589 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6671505 10752 RMVar_ID_10752 Human_SNP_ID_640135557 A-to-I Human chr18 + 21408683 21408683 21408683 AGGTGTGGTGGTGCATGCCTGTAATTCCAGCTAGTCGGGAGGCTGAGGCAGGAGAATCACTTGAA AGGTGTGGTGGTGCATGCCTGTAATTCCAGCTGGTCGGGAGGCTGAGGCAGGAGAATCACTTGAA A G GREB1L Ensembl:ENSG00000141449 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1316074932 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96986,RMVar_hsa_circ_188973,RMVar_hsa_circ_6645,RMVar_hsa_circ_188977,RMVar_hsa_circ_118716 10753 RMVar_ID_10753 Human_SNP_ID_640150640 A-to-I Human chr18 + 21475884 21475884 21475884 CCAGCTACTAGGGAGGCTGAAGCAGGAGAATCACTTGAACCCAGGAGGCAGAGGTTGCAGTGAGC CCAGCTACTAGGGAGGCTGAAGCAGGAGAATCGCTTGAACCCAGGAGGCAGAGGTTGCAGTGAGC A G GREB1L Ensembl:ENSG00000141449 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1179242306 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2440,RMVar_hsa_circ_96986,RMVar_hsa_circ_188973,RMVar_hsa_circ_365147,RMVar_hsa_circ_374269,RMVar_hsa_circ_125921,RMVar_hsa_circ_188979,RMVar_hsa_circ_188980,RMVar_hsa_circ_22516,RMVar_hsa_circ_46275,RMVar_hsa_circ_14363,RMVar_hsa_circ_110108,RMVar_hsa_circ_188981,RMVar_hsa_circ_341297,RMVar_hsa_circ_38890,RMVar_hsa_circ_61797,RMVar_hsa_circ_346491,RMVar_hsa_circ_28307 10754 RMVar_ID_10754 Human_SNP_ID_640170928 A-to-I Human chr18 - 21562541 21562541 21562541 AACCTCCCAGCCTCAAGTGATCCTCTCACCTCAGCCTGCTGAATAGCTGGGACTAACAGACATGC AACCTCCCAGCCTCAAGTGATCCTCTCACCTCGGCCTGCTGAATAGCTGGGACTAACAGACATGC T C ESCO1 Ensembl:ENSG00000141446 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs753707974 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_188987,RMVar_hsa_circ_4114,RMVar_hsa_circ_351029,RMVar_hsa_circ_277913,RMVar_hsa_circ_188985,RMVar_hsa_circ_327841,RMVar_hsa_circ_367621,RMVar_hsa_circ_324686,RMVar_hsa_circ_284087,RMVar_hsa_circ_188988,RMVar_hsa_circ_188992,RMVar_hsa_circ_127210,RMVar_hsa_circ_188986,RMVar_hsa_circ_325988,RMVar_hsa_circ_292371,RMVar_hsa_circ_39639,RMVar_hsa_circ_188993,RMVar_hsa_circ_188995,RMVar_hsa_circ_188997,RMVar_hsa_circ_281764,RMVar_hsa_circ_309681,RMVar_hsa_circ_291449,RMVar_hsa_circ_274285,RMVar_hsa_circ_188996,RMVar_hsa_circ_188994 10755 RMVar_ID_10755 Human_SNP_ID_640171058 A-to-I Human chr18 - 21563010 21563010 21563010 AAAATTAGCTGGGCGTGGTGATTCGTTCCTATAATCCCAGCTGCTCGGGAGGCTAAAACAGGAGA AAAATTAGCTGGGCGTGGTGATTCGTTCCTATCATCCCAGCTGCTCGGGAGGCTAAAACAGGAGA T G ESCO1 Ensembl:ENSG00000141446 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1294202164 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_188987,RMVar_hsa_circ_4114,RMVar_hsa_circ_351029,RMVar_hsa_circ_277913,RMVar_hsa_circ_188985,RMVar_hsa_circ_327841,RMVar_hsa_circ_367621,RMVar_hsa_circ_324686,RMVar_hsa_circ_284087,RMVar_hsa_circ_188988,RMVar_hsa_circ_188992,RMVar_hsa_circ_127210,RMVar_hsa_circ_188986,RMVar_hsa_circ_325988,RMVar_hsa_circ_292371,RMVar_hsa_circ_39639,RMVar_hsa_circ_188993,RMVar_hsa_circ_188995,RMVar_hsa_circ_188997,RMVar_hsa_circ_281764,RMVar_hsa_circ_309681,RMVar_hsa_circ_291449,RMVar_hsa_circ_274285,RMVar_hsa_circ_188996,RMVar_hsa_circ_188994 10756 RMVar_ID_10756 Human_SNP_ID_640171059 A-to-I Human chr18 - 21563012 21563012 21563012 ACAAAATTAGCTGGGCGTGGTGATTCGTTCCTATAATCCCAGCTGCTCGGGAGGCTAAAACAGGA ACAAAATTAGCTGGGCGTGGTGATTCGTTCCTGTAATCCCAGCTGCTCGGGAGGCTAAAACAGGA T C ESCO1 Ensembl:ENSG00000141446 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs551801339 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_188987,RMVar_hsa_circ_4114,RMVar_hsa_circ_351029,RMVar_hsa_circ_277913,RMVar_hsa_circ_188985,RMVar_hsa_circ_327841,RMVar_hsa_circ_367621,RMVar_hsa_circ_324686,RMVar_hsa_circ_284087,RMVar_hsa_circ_188988,RMVar_hsa_circ_188992,RMVar_hsa_circ_127210,RMVar_hsa_circ_188986,RMVar_hsa_circ_325988,RMVar_hsa_circ_292371,RMVar_hsa_circ_39639,RMVar_hsa_circ_188993,RMVar_hsa_circ_188995,RMVar_hsa_circ_188997,RMVar_hsa_circ_281764,RMVar_hsa_circ_309681,RMVar_hsa_circ_291449,RMVar_hsa_circ_274285,RMVar_hsa_circ_188996,RMVar_hsa_circ_188994 10757 RMVar_ID_10757 Human_SNP_ID_640171078 A-to-I Human chr18 - 21563074 21563074 21563074 CTGAGGGTGGGAGTTCAAGACCAGCCTGACCAACACCGAGAAAGCCCATCTCTACTAAAAATACA CTGAGGGTGGGAGTTCAAGACCAGCCTGACCAGCACCGAGAAAGCCCATCTCTACTAAAAATACA T C ESCO1 Ensembl:ENSG00000141446 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1019853200 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_188987,RMVar_hsa_circ_4114,RMVar_hsa_circ_351029,RMVar_hsa_circ_277913,RMVar_hsa_circ_188985,RMVar_hsa_circ_327841,RMVar_hsa_circ_367621,RMVar_hsa_circ_324686,RMVar_hsa_circ_284087,RMVar_hsa_circ_188988,RMVar_hsa_circ_188992,RMVar_hsa_circ_127210,RMVar_hsa_circ_188986,RMVar_hsa_circ_325988,RMVar_hsa_circ_292371,RMVar_hsa_circ_39639,RMVar_hsa_circ_188993,RMVar_hsa_circ_188995,RMVar_hsa_circ_188997,RMVar_hsa_circ_281764,RMVar_hsa_circ_309681,RMVar_hsa_circ_291449,RMVar_hsa_circ_274285,RMVar_hsa_circ_188996,RMVar_hsa_circ_188994 10758 RMVar_ID_10758 Human_SNP_ID_640172360 A-to-I Human chr18 - 21568084 21568084 21568084 ATTTTGAATTATATGTGTTCAGAATTTCAGCCAATGTTTGGAATCCAAGCTAGAAAACAGTCCAG ATTTTGAATTATATGTGTTCAGAATTTCAGCCGATGTTTGGAATCCAAGCTAGAAAACAGTCCAG T C ESCO1 Ensembl:ENSG00000141446 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs369112026 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1290171,Human_RBP_ID_2535446,Human_RBP_ID_13259210,Human_RBP_ID_23762157,Human_RBP_ID_25376639 Human_Splice_Rec_1898474,Human_Splice_Rec_1898496 RMVar_hsa_circ_188987,RMVar_hsa_circ_4114,RMVar_hsa_circ_277913,RMVar_hsa_circ_327841,RMVar_hsa_circ_284087,RMVar_hsa_circ_88986,RMVar_hsa_circ_127210,RMVar_hsa_circ_188986,RMVar_hsa_circ_325988,RMVar_hsa_circ_39639,RMVar_hsa_circ_188993,RMVar_hsa_circ_188995,RMVar_hsa_circ_281764,RMVar_hsa_circ_309681,RMVar_hsa_circ_274285,RMVar_hsa_circ_188996,RMVar_hsa_circ_189001,RMVar_hsa_circ_280742,RMVar_hsa_circ_293895,RMVar_hsa_circ_188994,RMVar_hsa_circ_291419,RMVar_hsa_circ_188999,RMVar_hsa_circ_189000,RMVar_hsa_circ_361755,RMVar_hsa_circ_292430,RMVar_hsa_circ_189003,RMVar_hsa_circ_189004,RMVar_hsa_circ_189005,RMVar_hsa_circ_338698,RMVar_hsa_circ_189002,RMVar_hsa_circ_322215 10759 RMVar_ID_10759 Human_SNP_ID_640173464 A-to-I Human chr18 - 21572802 21572802 21572802 GCATCACCATGCCTGGCTGATTTTGTATTTTTAGTAGAGACGGGGTTTCTCCATGTTGATCAGGC GCATCACCATGCCTGGCTGATTTTGTATTTTTGGTAGAGACGGGGTTTCTCCATGTTGATCAGGC T C ESCO1 Ensembl:ENSG00000141446 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs993928395 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4114,RMVar_hsa_circ_277913,RMVar_hsa_circ_327841,RMVar_hsa_circ_88986,RMVar_hsa_circ_127210,RMVar_hsa_circ_188986,RMVar_hsa_circ_39639,RMVar_hsa_circ_188993,RMVar_hsa_circ_188995,RMVar_hsa_circ_281764,RMVar_hsa_circ_274285,RMVar_hsa_circ_189001,RMVar_hsa_circ_293895,RMVar_hsa_circ_188994,RMVar_hsa_circ_291419,RMVar_hsa_circ_189000,RMVar_hsa_circ_361755,RMVar_hsa_circ_189003,RMVar_hsa_circ_189004,RMVar_hsa_circ_189005,RMVar_hsa_circ_338698,RMVar_hsa_circ_322215 10760 RMVar_ID_10760 Human_SNP_ID_640173465 A-to-I Human chr18 - 21572802 21572802 21572802 GCATCACCATGCCTGGCTGATTTTGTATTTTTAGTAGAGACGGGGTTTCTCCATGTTGATCAGGC GCATCACCATGCCTGGCTGATTTTGTATTTTTCGTAGAGACGGGGTTTCTCCATGTTGATCAGGC T G ESCO1 Ensembl:ENSG00000141446 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs993928395 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4114,RMVar_hsa_circ_277913,RMVar_hsa_circ_327841,RMVar_hsa_circ_88986,RMVar_hsa_circ_127210,RMVar_hsa_circ_188986,RMVar_hsa_circ_39639,RMVar_hsa_circ_188993,RMVar_hsa_circ_188995,RMVar_hsa_circ_281764,RMVar_hsa_circ_274285,RMVar_hsa_circ_189001,RMVar_hsa_circ_293895,RMVar_hsa_circ_188994,RMVar_hsa_circ_291419,RMVar_hsa_circ_189000,RMVar_hsa_circ_361755,RMVar_hsa_circ_189003,RMVar_hsa_circ_189004,RMVar_hsa_circ_189005,RMVar_hsa_circ_338698,RMVar_hsa_circ_322215 10761 RMVar_ID_10761 Human_SNP_ID_640175681 A-to-I Human chr18 - 21580126 21580126 21580126 GGGAAGCCGAGGCGGTTGGATTACCTAAAGTCAGGAGTTCGAGACCAGCCTGACCAATACACCGA GGGAAGCCGAGGCGGTTGGATTACCTAAAGTCGGGAGTTCGAGACCAGCCTGACCAATACACCGA T C ESCO1 Ensembl:ENSG00000141446 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1311236277 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4114,RMVar_hsa_circ_327841,RMVar_hsa_circ_88986,RMVar_hsa_circ_188986,RMVar_hsa_circ_39639,RMVar_hsa_circ_281764,RMVar_hsa_circ_189001,RMVar_hsa_circ_293895,RMVar_hsa_circ_188994,RMVar_hsa_circ_361755,RMVar_hsa_circ_189003,RMVar_hsa_circ_189004,RMVar_hsa_circ_189005,RMVar_hsa_circ_322215,RMVar_hsa_circ_293966 10762 RMVar_ID_10762 Human_SNP_ID_640176228 A-to-I Human chr18 - 21582326 21582326 21582326 ACTCGGGAGGCTGAGGCGGGAGACTCGCTTGAACCCAGGAGGCGGAGGATGCAGTGAGCCAAGAT ACTCGGGAGGCTGAGGCGGGAGACTCGCTTGAGCCCAGGAGGCGGAGGATGCAGTGAGCCAAGAT T C ESCO1 Ensembl:ENSG00000141446 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946091169 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4114,RMVar_hsa_circ_327841,RMVar_hsa_circ_88986,RMVar_hsa_circ_188986,RMVar_hsa_circ_39639,RMVar_hsa_circ_281764,RMVar_hsa_circ_189001,RMVar_hsa_circ_293895,RMVar_hsa_circ_188994,RMVar_hsa_circ_361755,RMVar_hsa_circ_189003,RMVar_hsa_circ_189004,RMVar_hsa_circ_189005,RMVar_hsa_circ_322215,RMVar_hsa_circ_293966 10763 RMVar_ID_10763 Human_SNP_ID_640176229 A-to-I Human chr18 - 21582326 21582326 21582326 ACTCGGGAGGCTGAGGCGGGAGACTCGCTTGAACCCAGGAGGCGGAGGATGCAGTGAGCCAAGAT ACTCGGGAGGCTGAGGCGGGAGACTCGCTTGACCCCAGGAGGCGGAGGATGCAGTGAGCCAAGAT T G ESCO1 Ensembl:ENSG00000141446 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946091169 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4114,RMVar_hsa_circ_327841,RMVar_hsa_circ_88986,RMVar_hsa_circ_188986,RMVar_hsa_circ_39639,RMVar_hsa_circ_281764,RMVar_hsa_circ_189001,RMVar_hsa_circ_293895,RMVar_hsa_circ_188994,RMVar_hsa_circ_361755,RMVar_hsa_circ_189003,RMVar_hsa_circ_189004,RMVar_hsa_circ_189005,RMVar_hsa_circ_322215,RMVar_hsa_circ_293966 10764 RMVar_ID_10764 Human_SNP_ID_640181041 A-to-I Human chr18 - 21599281 21599281 21599281 TGGATTGCAGTGGTGTAATCACTGTTCACTGCAGCCTTGACCTCCCTCCCCGGCCCCAAGCAATC TGGATTGCAGTGGTGTAATCACTGTTCACTGCGGCCTTGACCTCCCTCCCCGGCCCCAAGCAATC T C ESCO1 Ensembl:ENSG00000141446 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1016104377 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3551380,Human_RBP_ID_13259941 RMVar_hsa_circ_88986,RMVar_hsa_circ_189004 10765 RMVar_ID_10765 Human_SNP_ID_640185675 A-to-I Human chr18 + 21616621 21616621 21616621 CTTGTGATCCACCCGCCTTGGCCTCCCAAAGTACTGGGATTACAGGCGTGAGCCACCATGCCTGA CTTGTGATCCACCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCATGCCTGA A G SNRPD1 Ensembl:ENSG00000167088 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1365794157 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25352747 RMVar_hsa_circ_124957,RMVar_hsa_circ_189006 10766 RMVar_ID_10766 Human_SNP_ID_640185860 A-to-I Human chr18 + 21617318 21617318 21617318 GCTCTACTAAAACAAAAAGAAATACAAAAATTAGCTGGTTGTGGTGGCGAGTGCCTGTAATCCCA GCTCTACTAAAACAAAAAGAAATACAAAAATTGGCTGGTTGTGGTGGCGAGTGCCTGTAATCCCA A G SNRPD1 Ensembl:ENSG00000167088 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs79075147 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124957,RMVar_hsa_circ_189006 10767 RMVar_ID_10767 Human_SNP_ID_640186387 A-to-I Human chr18 + 21619273 21619273 21619273 GCAGTCTTGGCTCACTGCAACCTCTGCCTCCCAGGCTCAAGCAATTCTCCTGCCTCAGCCTCCCC GCAGTCTTGGCTCACTGCAACCTCTGCCTCCCGGGCTCAAGCAATTCTCCTGCCTCAGCCTCCCC A G SNRPD1 Ensembl:ENSG00000167088 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs998558004 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124957,RMVar_hsa_circ_189006 10768 RMVar_ID_10768 Human_SNP_ID_640188095 A-to-I Human chr18 + 21625386 21625386 21625386 TTAGCCAAGCTGGAGTGCAGTGGCAGGATCTCAGCTCACTGCAACCTCTGCCTCCTGGGTTCAAG TTAGCCAAGCTGGAGTGCAGTGGCAGGATCTCGGCTCACTGCAACCTCTGCCTCCTGGGTTCAAG A G SNRPD1 Ensembl:ENSG00000167088 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs867545511 Functional Loss SNV dbSNP153 33..33 33 - - - 10769 RMVar_ID_10769 Human_SNP_ID_640188244 A-to-I Human chr18 + 21625817 21625817 21625817 TATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAAGCGGTCTCGATCTCCTGACCTCATGAT TATTTTTAGTAGAGACGGGGTTTCACCGTGTTGGCCAAGCGGTCTCGATCTCCTGACCTCATGAT A G SNRPD1 Ensembl:ENSG00000167088 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs986698861 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13260368 10770 RMVar_ID_10770 Human_SNP_ID_640189496 A-to-I Human chr18 + 21630589 21630589 21630589 GAAGACCAGCTTGGCCAAGAGGGTGAAACCCCATTTCTACTAAAAATACAAAAGTTAGCCAGGTG GAAGACCAGCTTGGCCAAGAGGGTGAAACCCCGTTTCTACTAAAAATACAAAAGTTAGCCAGGTG A G SNRPD1 Ensembl:ENSG00000167088 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1276718531 Functional Loss SNV dbSNP153 33..33 33 - - - 10771 RMVar_ID_10771 Human_SNP_ID_640189499 A-to-I Human chr18 + 21630606 21630606 21630606 AGAGGGTGAAACCCCATTTCTACTAAAAATACAAAAGTTAGCCAGGTGCAGTGACAGGCGCCTGT AGAGGGTGAAACCCCATTTCTACTAAAAATACGAAAGTTAGCCAGGTGCAGTGACAGGCGCCTGT A G SNRPD1 Ensembl:ENSG00000167088 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs907917528 Functional Loss SNV dbSNP153 33..33 33 - - - 10772 RMVar_ID_10772 Human_SNP_ID_640189828 A-to-I Human chr18 + 21631643 21631643 21631643 TCTTTTTAGTAGAGACGGGGTTTCACTGTGTTAGGATGGTCTCGTTCTCCTGACCTCATGATCTG TCTTTTTAGTAGAGACGGGGTTTCACTGTGTTCGGATGGTCTCGTTCTCCTGACCTCATGATCTG A C SNRPD1 Ensembl:ENSG00000167088 Protein coding 3'UTR GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 29129909,30559470 RNA-Seq:(High) rs1002457567 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6672274,Human_RBP_ID_13260485,Human_RBP_ID_23762275 10773 RMVar_ID_10773 Human_SNP_ID_640189829 A-to-I Human chr18 + 21631643 21631643 21631643 TCTTTTTAGTAGAGACGGGGTTTCACTGTGTTAGGATGGTCTCGTTCTCCTGACCTCATGATCTG TCTTTTTAGTAGAGACGGGGTTTCACTGTGTTGGGATGGTCTCGTTCTCCTGACCTCATGATCTG A G SNRPD1 Ensembl:ENSG00000167088 Protein coding 3'UTR GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 29129909,30559470 RNA-Seq:(High) rs1002457567 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6672274,Human_RBP_ID_13260485,Human_RBP_ID_23762275 10774 RMVar_ID_10774 Human_SNP_ID_640189837 A-to-I Human chr18 + 21631668 21631668 21631668 CTGTGTTAGGATGGTCTCGTTCTCCTGACCTCATGATCTGCACGAGGCCTCCCAATGTGCTGGGA CTGTGTTAGGATGGTCTCGTTCTCCTGACCTCCTGATCTGCACGAGGCCTCCCAATGTGCTGGGA A C SNRPD1 Ensembl:ENSG00000167088 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs761314838 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6672274,Human_RBP_ID_13260486,Human_RBP_ID_23172872,Human_RBP_ID_23762275 10775 RMVar_ID_10775 Human_SNP_ID_640189838 A-to-I Human chr18 + 21631668 21631668 21631668 CTGTGTTAGGATGGTCTCGTTCTCCTGACCTCATGATCTGCACGAGGCCTCCCAATGTGCTGGGA CTGTGTTAGGATGGTCTCGTTCTCCTGACCTCGTGATCTGCACGAGGCCTCCCAATGTGCTGGGA A G SNRPD1 Ensembl:ENSG00000167088 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs761314838 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6672274,Human_RBP_ID_13260486,Human_RBP_ID_23172872,Human_RBP_ID_23762275 10776 RMVar_ID_10776 Human_SNP_ID_640189970 A-to-I Human chr18 + 21632237 21632236 21632237 GACCTCAGCACTTTGGGAGGCCGAGATGGGCGAATCACTTGAGGTCAGGAGTTCGAGACCAGCCT GACCTCAGCACTTTGGGAGGCCGAGATGGGCG_ATCACTTGAGGTCAGGAGTTCGAGACCAGCCT GA G SNRPD1 Ensembl:ENSG00000167088 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1207439375 Functional Loss DEL dbSNP153 33..33 33 - - - 10777 RMVar_ID_10777 Human_SNP_ID_640189979 A-to-I Human chr18 + 21632303 21632303 21632303 GGTAACATGGTGAAACCCTGTCTACTGAAAATACAAAAATTAGCTTGGTGTGGTGGCGGGTGCCT GGTAACATGGTGAAACCCTGTCTACTGAAAATGCAAAAATTAGCTTGGTGTGGTGGCGGGTGCCT A G SNRPD1 Ensembl:ENSG00000167088 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs182757456 Functional Loss SNV dbSNP153 33..33 33 - - - 10778 RMVar_ID_10778 Human_SNP_ID_640189980 A-to-I Human chr18 + 21632305 21632305 21632305 TAACATGGTGAAACCCTGTCTACTGAAAATACAAAAATTAGCTTGGTGTGGTGGCGGGTGCCTGT TAACATGGTGAAACCCTGTCTACTGAAAATACGAAAATTAGCTTGGTGTGGTGGCGGGTGCCTGT A G SNRPD1 Ensembl:ENSG00000167088 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs889511487 Functional Loss SNV dbSNP153 33..33 33 - - - 10779 RMVar_ID_10779 Human_SNP_ID_640189994 A-to-I Human chr18 + 21632352 21632352 21632352 GTGGTGGCGGGTGCCTGTAATCTCAGTTACTCAGGAGGCTTAGGCAGGAGAATCACTTGAACCCT GTGGTGGCGGGTGCCTGTAATCTCAGTTACTCGGGAGGCTTAGGCAGGAGAATCACTTGAACCCT A G SNRPD1 Ensembl:ENSG00000167088 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1194620697 Functional Loss SNV dbSNP153 33..33 33 - - - 10780 RMVar_ID_10780 Human_SNP_ID_640190221 A-to-I Human chr18 + 21633016 21633016 21633016 GAGACTACAGGTGCCCACCACTATGCCCGGCTAATGTTTTGTACTTTTAGTAGAGACGGGGTTTC GAGACTACAGGTGCCCACCACTATGCCCGGCTGATGTTTTGTACTTTTAGTAGAGACGGGGTTTC A G SNRPD1 Ensembl:ENSG00000167088 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1486212290 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6672314 10781 RMVar_ID_10781 Human_SNP_ID_640190235 A-to-I Human chr18 + 21633057 21633057 21633057 TACTTTTAGTAGAGACGGGGTTTCACTGTGTTAGCCAGGATGGTCTGAATCTCCTGACCTCGTGA TACTTTTAGTAGAGACGGGGTTTCACTGTGTTGGCCAGGATGGTCTGAATCTCCTGACCTCGTGA A G SNRPD1 Ensembl:ENSG00000167088 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1040968307 Functional Loss SNV dbSNP153 33..33 33 - - - 10782 RMVar_ID_10782 Human_SNP_ID_640195303 A-to-I Human chr18 - 21652609 21652609 21652609 CACCACGCCCATCCAATTTTTGTATTTTTAGTAGAGACGTGGTTTCACCATGTTGGCCAGGATGG CACCACGCCCATCCAATTTTTGTATTTTTAGTGGAGACGTGGTTTCACCATGTTGGCCAGGATGG T C ABHD3 Ensembl:ENSG00000158201 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs556034088 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_189008,RMVar_hsa_circ_92995 10783 RMVar_ID_10783 Human_SNP_ID_640195356 A-to-I Human chr18 - 21652820 21652820 21652820 TTGATCTCCTAACCTGGTCATCCACCTGCCTCAGCCTCCCAAAGTGCTGGGATGACAGGCGTGAG TTGATCTCCTAACCTGGTCATCCACCTGCCTCGGCCTCCCAAAGTGCTGGGATGACAGGCGTGAG T C ABHD3 Ensembl:ENSG00000158201 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1314969440 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_189008,RMVar_hsa_circ_92995 10784 RMVar_ID_10784 Human_SNP_ID_640195702 A-to-I Human chr18 - 21653904 21653904 21653904 GAGACAGAGGTTGCAGTAAGCCAGCCGAGATCACACCATTGCACTCCAGCCTGGGCAACAACAGT GAGACAGAGGTTGCAGTAAGCCAGCCGAGATCGCACCATTGCACTCCAGCCTGGGCAACAACAGT T C ABHD3 Ensembl:ENSG00000158201 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1436425208 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_189008,RMVar_hsa_circ_92995 10785 RMVar_ID_10785 Human_SNP_ID_640195711 A-to-I Human chr18 - 21653957 21653957 21653957 CCTGTGATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAACCCCGGAGACAGAGGTT CCTGTGATCCCAGCTACTCAGGAGGCTGAGGCGGGAGAATTGCTTGAACCCCGGAGACAGAGGTT T C ABHD3 Ensembl:ENSG00000158201 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1312368001 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_189008,RMVar_hsa_circ_92995 10786 RMVar_ID_10786 Human_SNP_ID_640195712 A-to-I Human chr18 - 21653974 21653974 21653974 GGCCGTGGTGGGACACACCTGTGATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAA GGCCGTGGTGGGACACACCTGTGATCCCAGCTGCTCAGGAGGCTGAGGCAGGAGAATTGCTTGAA T C ABHD3 Ensembl:ENSG00000158201 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs998811844 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_189008,RMVar_hsa_circ_92995 10787 RMVar_ID_10787 Human_SNP_ID_640195719 A-to-I Human chr18 - 21653990 21653990 21653990 AAATACAAAATTAGCTGGCCGTGGTGGGACACACCTGTGATCCCAGCTACTCAGGAGGCTGAGGC AAATACAAAATTAGCTGGCCGTGGTGGGACACGCCTGTGATCCCAGCTACTCAGGAGGCTGAGGC T C ABHD3 Ensembl:ENSG00000158201 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs967654753 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_189008,RMVar_hsa_circ_92995 10788 RMVar_ID_10788 Human_SNP_ID_640196028 A-to-I Human chr18 - 21655462 21655400 21655462 GCCCACGCAATGAAATTCCACCTCTATTAAAAATACAAAAATTAGCTGGGCATGGTGGCATGTGC GCCCACGCAATGAAATTCCACCTCTATTAAAA_________________________________ CCTCAGCCTCCCAAGTAGCTGGGATTACAGGCACATGCCACCATGCCCAGCTAATTTTTGTAT C ABHD3 Ensembl:ENSG00000158201 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1568134730 Functional Loss DEL dbSNP153 33..65 33 - - - Human_RBP_ID_135755 RMVar_hsa_circ_189008,RMVar_hsa_circ_92995 10789 RMVar_ID_10789 Human_SNP_ID_640196134 A-to-I Human chr18 - 21655808 21655808 21655808 TTTTGTTTTTTGAGATGGAGTCTCACTCTGCCACCCAGGCTGGAGTGCAAAGACACGATCTCGGC TTTTGTTTTTTGAGATGGAGTCTCACTCTGCCGCCCAGGCTGGAGTGCAAAGACACGATCTCGGC T C ABHD3 Ensembl:ENSG00000158201 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1436566323 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_189008,RMVar_hsa_circ_92995 10790 RMVar_ID_10790 Human_SNP_ID_640196136 A-to-I Human chr18 - 21655826 21655826 21655826 CCTTTTTTTTGTTTGTTTTTTTGTTTTTTGAGATGGAGTCTCACTCTGCCACCCAGGCTGGAGTG CCTTTTTTTTGTTTGTTTTTTTGTTTTTTGAGGTGGAGTCTCACTCTGCCACCCAGGCTGGAGTG T C ABHD3 Ensembl:ENSG00000158201 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1482057158 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_189008,RMVar_hsa_circ_92995 10791 RMVar_ID_10791 Human_SNP_ID_640197602 A-to-I Human chr18 - 21661403 21661403 21661403 TCAAACTCCTGACCTCATGATCTGCCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAG TCAAACTCCTGACCTCATGATCTGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAG T C ABHD3 Ensembl:ENSG00000158201 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1414990317 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63927,RMVar_hsa_circ_97754,RMVar_hsa_circ_189008,RMVar_hsa_circ_92995,RMVar_hsa_circ_330655,RMVar_hsa_circ_270195,RMVar_hsa_circ_189011,RMVar_hsa_circ_189012,RMVar_hsa_circ_314693,RMVar_hsa_circ_189013,RMVar_hsa_circ_367710 10792 RMVar_ID_10792 Human_SNP_ID_640197603 A-to-I Human chr18 - 21661403 21661403 21661403 TCAAACTCCTGACCTCATGATCTGCCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAG TCAAACTCCTGACCTCATGATCTGCCTGCCTCCGCCTCCCAAAGTGCTGGGATTACAGGCATGAG T G ABHD3 Ensembl:ENSG00000158201 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1414990317 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63927,RMVar_hsa_circ_97754,RMVar_hsa_circ_189008,RMVar_hsa_circ_92995,RMVar_hsa_circ_330655,RMVar_hsa_circ_270195,RMVar_hsa_circ_189011,RMVar_hsa_circ_189012,RMVar_hsa_circ_314693,RMVar_hsa_circ_189013,RMVar_hsa_circ_367710 10793 RMVar_ID_10793 Human_SNP_ID_640197813 A-to-I Human chr18 - 21662236 21662232 21662236 GCCGGGCATGATGGTGCATGCTTGTAATCCCAACACGCTGGGAGGCCAAGGCGGGCAGATCATCT GCCGGGCATGATGGTGCATGCTTGTAATCCCA____GCTGGGAGGCCAAGGCGGGCAGATCATCT CGTGT C ABHD3,AC106037.2 Ensembl:ENSG00000158201,Ensembl:ENSG00000264188 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1377030366 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_63927,RMVar_hsa_circ_97754,RMVar_hsa_circ_189008,RMVar_hsa_circ_92995,RMVar_hsa_circ_330655,RMVar_hsa_circ_270195,RMVar_hsa_circ_189011,RMVar_hsa_circ_189012,RMVar_hsa_circ_314693,RMVar_hsa_circ_189013,RMVar_hsa_circ_367710 10794 RMVar_ID_10794 Human_SNP_ID_640198480 A-to-I Human chr18 - 21664901 21664901 21664901 GGGCCAGGCACAGGCTCACACCTATAATCCCAACACGTTGGGGGGCCAAAGCAGGTGAATCACTG GGGCCAGGCACAGGCTCACACCTATAATCCCAGCACGTTGGGGGGCCAAAGCAGGTGAATCACTG T C ABHD3 Ensembl:ENSG00000158201 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909985451 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63927,RMVar_hsa_circ_97754,RMVar_hsa_circ_330655,RMVar_hsa_circ_189012 10795 RMVar_ID_10795 Human_SNP_ID_640198801 A-to-I Human chr18 - 21666149 21666149 21666149 CACACCTGCAGTCCCAGCTACTCAGGAAGCTAAGGCAGGAGAATTGCTTGAACCCAGGAGGCAGA CACACCTGCAGTCCCAGCTACTCAGGAAGCTAGGGCAGGAGAATTGCTTGAACCCAGGAGGCAGA T C ABHD3 Ensembl:ENSG00000158201 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1010303936 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63927,RMVar_hsa_circ_97754,RMVar_hsa_circ_330655,RMVar_hsa_circ_189012 10796 RMVar_ID_10796 Human_SNP_ID_640199620 A-to-I Human chr18 - 21669151 21669151 21669151 AAGGCTGGAGTGCAGTGTCATGATCACAGCTCACTGCAGCCTCTACCTCCCAGTCTCAGGTGATC AAGGCTGGAGTGCAGTGTCATGATCACAGCTCGCTGCAGCCTCTACCTCCCAGTCTCAGGTGATC T C ABHD3 Ensembl:ENSG00000158201 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1392896397 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63927,RMVar_hsa_circ_97754,RMVar_hsa_circ_330655,RMVar_hsa_circ_189012 10797 RMVar_ID_10797 Human_SNP_ID_640202684 A-to-I Human chr18 - 21682054 21682054 21682054 TGGCTCACTGTAGCCTCGACCGCCTGGGCTCAAGTGATCCTTCCACCTCAGCTTCCCAAGTAGGT TGGCTCACTGTAGCCTCGACCGCCTGGGCTCAGGTGATCCTTCCACCTCAGCTTCCCAAGTAGGT T C ABHD3 Ensembl:ENSG00000158201 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1301625401 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63927,RMVar_hsa_circ_97754,RMVar_hsa_circ_330655,RMVar_hsa_circ_189012 10798 RMVar_ID_10798 Human_SNP_ID_640210786 A-to-I Human chr18 + 21713216 21713216 21713216 GTCTTGAACTCCTGGCCTTAAACAATCCCCCCATCTCAGACTCCCAAAGTGCTGGGATTACAACC GTCTTGAACTCCTGGCCTTAAACAATCCCCCCGTCTCAGACTCCCAAAGTGCTGGGATTACAACC A G MIB1 Ensembl:ENSG00000101752 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1367817476 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82071,RMVar_hsa_circ_102856,RMVar_hsa_circ_189017,RMVar_hsa_circ_189018 10799 RMVar_ID_10799 Human_SNP_ID_640212517 A-to-I Human chr18 + 21720739 21720739 21720739 GGGAGGCTGAGAGGGGTAAATTGCTTGAGGCCAAGAGTTTGAGATCAGTCTGGGGAACAGAGGGG GGGAGGCTGAGAGGGGTAAATTGCTTGAGGCCCAGAGTTTGAGATCAGTCTGGGGAACAGAGGGG A C MIB1 Ensembl:ENSG00000101752 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1353771553 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82071,RMVar_hsa_circ_102856,RMVar_hsa_circ_189017,RMVar_hsa_circ_189018 10800 RMVar_ID_10800 Human_SNP_ID_640225882 A-to-I Human chr18 + 21774402 21774402 21774402 CTTGAAGTCAGGAGTTTGAGATCACACTGGCCAACATGGTGAAACCCTGTCTTTACTAAAATACA CTTGAAGTCAGGAGTTTGAGATCACACTGGCCCACATGGTGAAACCCTGTCTTTACTAAAATACA A C MIB1 Ensembl:ENSG00000101752 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs776164228 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100558,RMVar_hsa_circ_189023,RMVar_hsa_circ_272479,RMVar_hsa_circ_333667,RMVar_hsa_circ_82071,RMVar_hsa_circ_189018,RMVar_hsa_circ_361969,RMVar_hsa_circ_373427,RMVar_hsa_circ_373922,RMVar_hsa_circ_369867,RMVar_hsa_circ_346305,RMVar_hsa_circ_283462,RMVar_hsa_circ_333069,RMVar_hsa_circ_292415,RMVar_hsa_circ_278020,RMVar_hsa_circ_273543,RMVar_hsa_circ_49405,RMVar_hsa_circ_272460,RMVar_hsa_circ_65888,RMVar_hsa_circ_189027,RMVar_hsa_circ_189029,RMVar_hsa_circ_189028,RMVar_hsa_circ_189025,RMVar_hsa_circ_189026,RMVar_hsa_circ_189024,RMVar_hsa_circ_189019,RMVar_hsa_circ_189021,RMVar_hsa_circ_189022,RMVar_hsa_circ_189020,RMVar_hsa_circ_189036,RMVar_hsa_circ_104879,RMVar_hsa_circ_315671,RMVar_hsa_circ_112582,RMVar_hsa_circ_79924,RMVar_hsa_circ_189037,RMVar_hsa_circ_189034,RMVar_hsa_circ_189035,RMVar_hsa_circ_336147,RMVar_hsa_circ_375804,RMVar_hsa_circ_270208,RMVar_hsa_circ_189038,RMVar_hsa_circ_63468,RMVar_hsa_circ_87865,RMVar_hsa_circ_189040,RMVar_hsa_circ_189041,RMVar_hsa_circ_189042,RMVar_hsa_circ_189039 10801 RMVar_ID_10801 Human_SNP_ID_640234030 A-to-I Human chr18 + 21807309 21807309 21807309 AAAACATTAGCCAGGTGTGCTGGCACACAGCTATAGTCTCTTCTACTTGGAAGGCTGAGGTGGGA AAAACATTAGCCAGGTGTGCTGGCACACAGCTGTAGTCTCTTCTACTTGGAAGGCTGAGGTGGGA A G MIB1 Ensembl:ENSG00000101752 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459482672 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100558,RMVar_hsa_circ_189023,RMVar_hsa_circ_333667,RMVar_hsa_circ_361969,RMVar_hsa_circ_373427,RMVar_hsa_circ_373922,RMVar_hsa_circ_369867,RMVar_hsa_circ_346305,RMVar_hsa_circ_283462,RMVar_hsa_circ_333069,RMVar_hsa_circ_65888,RMVar_hsa_circ_189024,RMVar_hsa_circ_189019,RMVar_hsa_circ_189021,RMVar_hsa_circ_189022,RMVar_hsa_circ_189020,RMVar_hsa_circ_189036,RMVar_hsa_circ_112582,RMVar_hsa_circ_79924,RMVar_hsa_circ_189037,RMVar_hsa_circ_375804,RMVar_hsa_circ_2888,RMVar_hsa_circ_3723,RMVar_hsa_circ_189038,RMVar_hsa_circ_87865,RMVar_hsa_circ_189040,RMVar_hsa_circ_189039,RMVar_hsa_circ_375402,RMVar_hsa_circ_367452,RMVar_hsa_circ_105029,RMVar_hsa_circ_125094,RMVar_hsa_circ_43336,RMVar_hsa_circ_51404,RMVar_hsa_circ_189047,RMVar_hsa_circ_3548,RMVar_hsa_circ_189048,RMVar_hsa_circ_189046,RMVar_hsa_circ_282407,RMVar_hsa_circ_304777,RMVar_hsa_circ_344208,RMVar_hsa_circ_304155,RMVar_hsa_circ_106485,RMVar_hsa_circ_189054,RMVar_hsa_circ_189055,RMVar_hsa_circ_189053,RMVar_hsa_circ_265464,RMVar_hsa_circ_28914,RMVar_hsa_circ_189057,RMVar_hsa_circ_90379,RMVar_hsa_circ_189058,RMVar_hsa_circ_373548,RMVar_hsa_circ_189060,RMVar_hsa_circ_370089,RMVar_hsa_circ_74050,RMVar_hsa_circ_189061,RMVar_hsa_circ_189063 10802 RMVar_ID_10802 Human_SNP_ID_640235648 A-to-I Human chr18 + 21814460 21814460 21814460 TCTTTGTAGGACGTGCACGGTGGCTCACACCTATGATCCCAGCATTTTGTGAGGCTGAAGTTGGA TCTTTGTAGGACGTGCACGGTGGCTCACACCTCTGATCCCAGCATTTTGTGAGGCTGAAGTTGGA A C MIB1 Ensembl:ENSG00000101752 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1463693154 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25353291 RMVar_hsa_circ_100558,RMVar_hsa_circ_189023,RMVar_hsa_circ_333667,RMVar_hsa_circ_361969,RMVar_hsa_circ_373427,RMVar_hsa_circ_373922,RMVar_hsa_circ_369867,RMVar_hsa_circ_346305,RMVar_hsa_circ_283462,RMVar_hsa_circ_333069,RMVar_hsa_circ_65888,RMVar_hsa_circ_189024,RMVar_hsa_circ_189019,RMVar_hsa_circ_189021,RMVar_hsa_circ_189022,RMVar_hsa_circ_189020,RMVar_hsa_circ_189036,RMVar_hsa_circ_112582,RMVar_hsa_circ_79924,RMVar_hsa_circ_189037,RMVar_hsa_circ_375804,RMVar_hsa_circ_2888,RMVar_hsa_circ_3723,RMVar_hsa_circ_189038,RMVar_hsa_circ_87865,RMVar_hsa_circ_189040,RMVar_hsa_circ_189039,RMVar_hsa_circ_375402,RMVar_hsa_circ_367452,RMVar_hsa_circ_105029,RMVar_hsa_circ_125094,RMVar_hsa_circ_43336,RMVar_hsa_circ_51404,RMVar_hsa_circ_189047,RMVar_hsa_circ_3548,RMVar_hsa_circ_189048,RMVar_hsa_circ_189046,RMVar_hsa_circ_282407,RMVar_hsa_circ_304777,RMVar_hsa_circ_344208,RMVar_hsa_circ_304155,RMVar_hsa_circ_106485,RMVar_hsa_circ_189054,RMVar_hsa_circ_189055,RMVar_hsa_circ_189053,RMVar_hsa_circ_265464,RMVar_hsa_circ_28914,RMVar_hsa_circ_189057,RMVar_hsa_circ_90379,RMVar_hsa_circ_189058,RMVar_hsa_circ_373548,RMVar_hsa_circ_189060,RMVar_hsa_circ_370089,RMVar_hsa_circ_74050,RMVar_hsa_circ_189061,RMVar_hsa_circ_189063 10803 RMVar_ID_10803 Human_SNP_ID_640333582 A-to-I Human chr18 + 22207829 22207829 22207829 CACCGCTGCACCCAGCTAATTTTTGTATTTTTAGTAAAGATGGGGCTTCTCCATGTTGGTCAGGC CACCGCTGCACCCAGCTAATTTTTGTATTTTTGGTAAAGATGGGGCTTCTCCATGTTGGTCAGGC A G HSALNG0120355 RNACentral:URS0000EA0B03 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1426326566 Functional Loss SNV dbSNP153 33..33 33 - - - 10804 RMVar_ID_10804 Human_SNP_ID_640522222 A-to-I Human chr18 + 23006595 23006595 23006595 GTAAACTCAGCTCACTGCAACCTCTGCCTCCTAGGCTCAAGCAATACTCCCACCTCAGCCTCCTG GTAAACTCAGCTCACTGCAACCTCTGCCTCCTGGGCTCAAGCAATACTCCCACCTCAGCCTCCTG A G RBBP8 Ensembl:ENSG00000101773 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1161923080 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107237,RMVar_hsa_circ_30451,RMVar_hsa_circ_189073,RMVar_hsa_circ_14490,RMVar_hsa_circ_25744,RMVar_hsa_circ_14620,RMVar_hsa_circ_189095,RMVar_hsa_circ_298890,RMVar_hsa_circ_338916 10805 RMVar_ID_10805 Human_SNP_ID_640524724 A-to-I Human chr18 + 23016439 23016439 23016439 GGTGGTACAGGCCTGTAATCCCAGCTACGCAGAAGGCTGAGGCACAAGAGTCGCTTGAACCTGGG GGTGGTACAGGCCTGTAATCCCAGCTACGCAGGAGGCTGAGGCACAAGAGTCGCTTGAACCTGGG A G RBBP8 Ensembl:ENSG00000101773 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1401998266 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18714975 RMVar_hsa_circ_107237,RMVar_hsa_circ_30451,RMVar_hsa_circ_189073,RMVar_hsa_circ_14490,RMVar_hsa_circ_25744,RMVar_hsa_circ_14620,RMVar_hsa_circ_189095,RMVar_hsa_circ_298890,RMVar_hsa_circ_338916 10806 RMVar_ID_10806 Human_SNP_ID_640524873 A-to-I Human chr18 + 23017099 23017099 23017099 ATTCTGGGTCGGGTGCGGTGGCTCATGCCTCTAATCTCAGCATTTTGGGAGGCCAAGGAGGGCGG ATTCTGGGTCGGGTGCGGTGGCTCATGCCTCTGATCTCAGCATTTTGGGAGGCCAAGGAGGGCGG A G RBBP8 Ensembl:ENSG00000101773 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs546394345 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107237,RMVar_hsa_circ_189073,RMVar_hsa_circ_14490,RMVar_hsa_circ_25744,RMVar_hsa_circ_14620,RMVar_hsa_circ_189095,RMVar_hsa_circ_298890,RMVar_hsa_circ_365595 10807 RMVar_ID_10807 Human_SNP_ID_640525172 A-to-I Human chr18 + 23018115 23018115 23018115 CTCTTGTTGCCTAGGCTGGAGCACAATAGTGCAATCTCAGCTCACCACAACCTCCATTTCCCGGG CTCTTGTTGCCTAGGCTGGAGCACAATAGTGCCATCTCAGCTCACCACAACCTCCATTTCCCGGG A C RBBP8 Ensembl:ENSG00000101773 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs908677436 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107237,RMVar_hsa_circ_189073,RMVar_hsa_circ_14490,RMVar_hsa_circ_25744,RMVar_hsa_circ_14620,RMVar_hsa_circ_189095,RMVar_hsa_circ_298890,RMVar_hsa_circ_365595 10808 RMVar_ID_10808 Human_SNP_ID_640525173 A-to-I Human chr18 + 23018121 23018120 23018121 TTGCCTAGGCTGGAGCACAATAGTGCAATCTCAGCTCACCACAACCTCCATTTCCCGGGTTCAGA TTGCCTAGGCTGGAGCACAATAGTGCAATCTC_GCTCACCACAACCTCCATTTCCCGGGTTCAGA CA C RBBP8 Ensembl:ENSG00000101773 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1191443526 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_107237,RMVar_hsa_circ_189073,RMVar_hsa_circ_14490,RMVar_hsa_circ_25744,RMVar_hsa_circ_14620,RMVar_hsa_circ_189095,RMVar_hsa_circ_298890,RMVar_hsa_circ_365595 10809 RMVar_ID_10809 Human_SNP_ID_640525174 A-to-I Human chr18 + 23018121 23018121 23018121 TTGCCTAGGCTGGAGCACAATAGTGCAATCTCAGCTCACCACAACCTCCATTTCCCGGGTTCAGA TTGCCTAGGCTGGAGCACAATAGTGCAATCTCCGCTCACCACAACCTCCATTTCCCGGGTTCAGA A C RBBP8 Ensembl:ENSG00000101773 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1175313807 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107237,RMVar_hsa_circ_189073,RMVar_hsa_circ_14490,RMVar_hsa_circ_25744,RMVar_hsa_circ_14620,RMVar_hsa_circ_189095,RMVar_hsa_circ_298890,RMVar_hsa_circ_365595 10810 RMVar_ID_10810 Human_SNP_ID_640554827 A-to-I Human chr18 - 23133425 23133425 23133425 AATTTGGCCTGGCACGGTGGCTAAAGCCTGTAATCCCAGCACTTTAGGAGGCCGAGGCAGGCAGA AATTTGGCCTGGCACGGTGGCTAAAGCCTGTAGTCCCAGCACTTTAGGAGGCCGAGGCAGGCAGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs373287225 Functional Loss SNV dbSNP153 33..33 33 - - - 10811 RMVar_ID_10811 Human_SNP_ID_640576093 A-to-I Human chr18 + 23217105 23217105 23217105 TTTTGTTTTTTGTTTTTGTTTGTTTTTGAGACAGGATTTTGCTTTGTTGCCCAGGCTGGAATGCA TTTTGTTTTTTGTTTTTGTTTGTTTTTGAGACGGGATTTTGCTTTGTTGCCCAGGCTGGAATGCA A G CABLES1 Ensembl:ENSG00000134508 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1330535509 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9079239,Human_RBP_ID_22962650 RMVar_hsa_circ_78919,RMVar_hsa_circ_189096,RMVar_hsa_circ_81692,RMVar_hsa_circ_189097,RMVar_hsa_circ_344144 10812 RMVar_ID_10812 Human_SNP_ID_640576115 A-to-I Human chr18 + 23217215 23217215 23217215 GCCATCCACCTGCCTCAGTCTCCCAAGTAGCTAGGACTACAGTCGCGCGCCACCACACCCAGCTA GCCATCCACCTGCCTCAGTCTCCCAAGTAGCTGGGACTACAGTCGCGCGCCACCACACCCAGCTA A G CABLES1 Ensembl:ENSG00000134508 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs552740352 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78919,RMVar_hsa_circ_189096,RMVar_hsa_circ_81692,RMVar_hsa_circ_189097,RMVar_hsa_circ_344144 10813 RMVar_ID_10813 Human_SNP_ID_640595781 A-to-I Human chr18 - 23294753 23294752 23294753 TTGTTTGTTGTTTTGTTTCGTTTGCTTGAGATAGGGGTTCACTGTGTTACCCAGGCTCGAGTGCA TTGTTTGTTGTTTTGTTTCGTTTGCTTGAGAT_GGGGTTCACTGTGTTACCCAGGCTCGAGTGCA CT C TMEM241 Ensembl:ENSG00000134490 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1487562764 Functional Loss DEL dbSNP153 33..33 33 - - - 10814 RMVar_ID_10814 Human_SNP_ID_640596363 A-to-I Human chr18 - 23297499 23297496 23297500 ATTATTATTTTTTAGAGACAAGGCCTCACTCTATCGCCTAGGCTGAAGCACAGTGGTGCGATCAC ATTATTATTTTTTAGAGACAAGGCCTCACTC____GCCTAGGCTGAAGCACAGTGGTGCGATCAC CGATA C TMEM241 Ensembl:ENSG00000134490 Protein coding intron GSE47997;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs999263585 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_24418058 Human_miRNA_ID_2237713 RMVar_hsa_circ_125163,RMVar_hsa_circ_189102 10815 RMVar_ID_10815 Human_SNP_ID_640596365 A-to-I Human chr18 - 23297499 23297499 23297499 ATTATTATTTTTTAGAGACAAGGCCTCACTCTATCGCCTAGGCTGAAGCACAGTGGTGCGATCAC ATTATTATTTTTTAGAGACAAGGCCTCACTCTGTCGCCTAGGCTGAAGCACAGTGGTGCGATCAC T C TMEM241 Ensembl:ENSG00000134490 Protein coding intron GSE47997;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs976069144 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24418058 Human_miRNA_ID_2237713 RMVar_hsa_circ_125163,RMVar_hsa_circ_189102 10816 RMVar_ID_10816 Human_SNP_ID_640639226 A-to-I Human chr18 + 23479777 23479777 23479777 TTTTGTATTTTTGGTAGAGACAGGGTTTCGCCATGTTGGCCAGGCCGGTCTTGAACTCCTGGCCT TTTTGTATTTTTGGTAGAGACAGGGTTTCGCCTTGTTGGCCAGGCCGGTCTTGAACTCCTGGCCT A T RIOK3 Ensembl:ENSG00000101782 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1441617333 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5189347 RMVar_hsa_circ_118363,RMVar_hsa_circ_189114,RMVar_hsa_circ_115291,RMVar_hsa_circ_86074,RMVar_hsa_circ_189120,RMVar_hsa_circ_189121 10817 RMVar_ID_10817 Human_SNP_ID_640646448 A-to-I Human chr18 + 23506623 23506623 23506623 TAATGAATGTGCTGTGAGATGCACAAGTAGATAGTTCTTTCCAGAAGCTTTGCTGTGAGAGAGAA TAATGAATGTGCTGTGAGATGCACAAGTAGATCGTTCTTTCCAGAAGCTTTGCTGTGAGAGAGAA A C RMC1 Ensembl:ENSG00000141452 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs745859655 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10270,RMVar_hsa_circ_74415,RMVar_hsa_circ_302377,RMVar_hsa_circ_358484,RMVar_hsa_circ_347857,RMVar_hsa_circ_293886,RMVar_hsa_circ_60715,RMVar_hsa_circ_189122 10818 RMVar_ID_10818 Human_SNP_ID_640646449 A-to-I Human chr18 + 23506623 23506623 23506623 TAATGAATGTGCTGTGAGATGCACAAGTAGATAGTTCTTTCCAGAAGCTTTGCTGTGAGAGAGAA TAATGAATGTGCTGTGAGATGCACAAGTAGATGGTTCTTTCCAGAAGCTTTGCTGTGAGAGAGAA A G RMC1 Ensembl:ENSG00000141452 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs745859655 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10270,RMVar_hsa_circ_74415,RMVar_hsa_circ_302377,RMVar_hsa_circ_358484,RMVar_hsa_circ_347857,RMVar_hsa_circ_293886,RMVar_hsa_circ_60715,RMVar_hsa_circ_189122 10819 RMVar_ID_10819 Human_SNP_ID_640658583 A-to-I Human chr18 - 23548902 23548902 23548902 ACCTTTAGTCCCAGCTACTGGGAGGCTGAGGCAGGAGGATTAATTGAGTTCGGGTGGTCAAGGCC ACCTTTAGTCCCAGCTACTGGGAGGCTGAGGCGGGAGGATTAATTGAGTTCGGGTGGTCAAGGCC T C NPC1 Ensembl:ENSG00000141458 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1273339930 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103140,RMVar_hsa_circ_69287,RMVar_hsa_circ_88333,RMVar_hsa_circ_189141,RMVar_hsa_circ_109217,RMVar_hsa_circ_83958,RMVar_hsa_circ_78289,RMVar_hsa_circ_189145,RMVar_hsa_circ_189147,RMVar_hsa_circ_189146,RMVar_hsa_circ_189144,RMVar_hsa_circ_189154,RMVar_hsa_circ_375236,RMVar_hsa_circ_366832 10820 RMVar_ID_10820 Human_SNP_ID_640661647 A-to-I Human chr18 - 23559932 23559932 23559932 TTTTTGGAGACTGAGTCTCACTCTTGTCGCCCAGGCTGAAGTGCAGTGGTGTGATCTCAGCTCAC TTTTTGGAGACTGAGTCTCACTCTTGTCGCCCGGGCTGAAGTGCAGTGGTGTGATCTCAGCTCAC T C NPC1 Ensembl:ENSG00000141458 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1400488082 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103140,RMVar_hsa_circ_189141,RMVar_hsa_circ_109217,RMVar_hsa_circ_83958,RMVar_hsa_circ_78289,RMVar_hsa_circ_189145,RMVar_hsa_circ_189146,RMVar_hsa_circ_189144,RMVar_hsa_circ_56713,RMVar_hsa_circ_189154,RMVar_hsa_circ_375236,RMVar_hsa_circ_371175,RMVar_hsa_circ_358091,RMVar_hsa_circ_314549,RMVar_hsa_circ_189156,RMVar_hsa_circ_189157,RMVar_hsa_circ_343460,RMVar_hsa_circ_298113 10821 RMVar_ID_10821 Human_SNP_ID_640674728 A-to-I Human chr18 - 23611496 23611496 23611496 GTGTTTTAGTAGAGACGGGGTTTCACCATGTTAGCCAGGCTGGTCTTGAACTCCTGACCTCAAGT GTGTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGACCTCAAGT T C ANKRD29 Ensembl:ENSG00000154065 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1362872557 Functional Loss SNV dbSNP153 33..33 33 - - - 10822 RMVar_ID_10822 Human_SNP_ID_640675295 A-to-I Human chr18 - 23613711 23613711 23613711 CCTGTAGTGCCAGCTACTTGGAAGACTGAGGCAGGAGAATGGCGTGAACCCGGGAGGCAGAGCTT CCTGTAGTGCCAGCTACTTGGAAGACTGAGGCGGGAGAATGGCGTGAACCCGGGAGGCAGAGCTT T C ANKRD29 Ensembl:ENSG00000154065 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs980207545 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33159,RMVar_hsa_circ_298970,RMVar_hsa_circ_300699 10823 RMVar_ID_10823 Human_SNP_ID_640768156 A-to-I Human chr18 + 24020537 24020537 24020537 ATGGGGGATTGGTTCCAGGACCCCCAGCGGATACCAAAATCTGTGGATGCTCAAATCCCTGATAG ATGGGGGATTGGTTCCAGGACCCCCAGCGGATCCCAAAATCTGTGGATGCTCAAATCCCTGATAG A C TTC39C Ensembl:ENSG00000168234 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1461896890 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101898,RMVar_hsa_circ_189245,RMVar_hsa_circ_189246,RMVar_hsa_circ_95582,RMVar_hsa_circ_99362,RMVar_hsa_circ_189247 10824 RMVar_ID_10824 Human_SNP_ID_640768157 A-to-I Human chr18 + 24020537 24020537 24020537 ATGGGGGATTGGTTCCAGGACCCCCAGCGGATACCAAAATCTGTGGATGCTCAAATCCCTGATAG ATGGGGGATTGGTTCCAGGACCCCCAGCGGATGCCAAAATCTGTGGATGCTCAAATCCCTGATAG A G TTC39C Ensembl:ENSG00000168234 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1461896890 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101898,RMVar_hsa_circ_189245,RMVar_hsa_circ_189246,RMVar_hsa_circ_95582,RMVar_hsa_circ_99362,RMVar_hsa_circ_189247 10825 RMVar_ID_10825 Human_SNP_ID_640780364 A-to-I Human chr18 + 24070984 24070983 24070984 GGAGTCTCGCAGTGTTTCCTTGGTTGGAGTGCAGTGGTGCGATCTTGGTTCACTGCAACCTCTGC GGAGTCTCGCAGTGTTTCCTTGGTTGGAGTGC_GTGGTGCGATCTTGGTTCACTGCAACCTCTGC CA C TTC39C Ensembl:ENSG00000168234 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1169210991 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_72512,RMVar_hsa_circ_68827,RMVar_hsa_circ_101898,RMVar_hsa_circ_189245,RMVar_hsa_circ_95582,RMVar_hsa_circ_189247,RMVar_hsa_circ_304158,RMVar_hsa_circ_329102,RMVar_hsa_circ_368637,RMVar_hsa_circ_297157,RMVar_hsa_circ_270652,RMVar_hsa_circ_189250,RMVar_hsa_circ_189252,RMVar_hsa_circ_189253,RMVar_hsa_circ_189251,RMVar_hsa_circ_110673,RMVar_hsa_circ_189255,RMVar_hsa_circ_81403,RMVar_hsa_circ_189254 10826 RMVar_ID_10826 Human_SNP_ID_640784846 A-to-I Human chr18 + 24090948 24090948 24090948 CATGCCTCAGCCTACCAAGTAGCTGAGACTACAGGTGTGCGCCACCATGCCTGGCTAATTTTTGT CATGCCTCAGCCTACCAAGTAGCTGAGACTACTGGTGTGCGCCACCATGCCTGGCTAATTTTTGT A T TTC39C Ensembl:ENSG00000168234 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1220511707 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_304158,RMVar_hsa_circ_329102,RMVar_hsa_circ_368637,RMVar_hsa_circ_297157,RMVar_hsa_circ_189252,RMVar_hsa_circ_189253,RMVar_hsa_circ_189251,RMVar_hsa_circ_110673,RMVar_hsa_circ_189254,RMVar_hsa_circ_189261,RMVar_hsa_circ_189259,RMVar_hsa_circ_340544,RMVar_hsa_circ_347169,RMVar_hsa_circ_28987,RMVar_hsa_circ_189258,RMVar_hsa_circ_286500,RMVar_hsa_circ_336438,RMVar_hsa_circ_368167,RMVar_hsa_circ_373890,RMVar_hsa_circ_324350,RMVar_hsa_circ_267392,RMVar_hsa_circ_189263,RMVar_hsa_circ_189264,RMVar_hsa_circ_189262 10827 RMVar_ID_10827 Human_SNP_ID_640788991 A-to-I Human chr18 + 24107777 24107777 24107777 TAGACTAATACACTAACAAACTTTTGTTTTTGAGACAGGGTCTCCCTCTGCCACCCAGGCGGGAG TAGACTAATACACTAACAAACTTTTGTTTTTGGGACAGGGTCTCCCTCTGCCACCCAGGCGGGAG A G TTC39C Ensembl:ENSG00000168234 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1363450164 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13269683 RMVar_hsa_circ_304158,RMVar_hsa_circ_329102,RMVar_hsa_circ_368637,RMVar_hsa_circ_297157,RMVar_hsa_circ_189252,RMVar_hsa_circ_189253,RMVar_hsa_circ_189251,RMVar_hsa_circ_110673,RMVar_hsa_circ_189254,RMVar_hsa_circ_189261,RMVar_hsa_circ_189259,RMVar_hsa_circ_340544,RMVar_hsa_circ_347169,RMVar_hsa_circ_28987,RMVar_hsa_circ_189258,RMVar_hsa_circ_286500,RMVar_hsa_circ_336438,RMVar_hsa_circ_368167,RMVar_hsa_circ_373890,RMVar_hsa_circ_324350,RMVar_hsa_circ_267392,RMVar_hsa_circ_189263,RMVar_hsa_circ_189264,RMVar_hsa_circ_189262 10828 RMVar_ID_10828 Human_SNP_ID_640801973 A-to-I Human chr18 + 24159277 24159277 24159277 ACTGTAGTGTCCCTGCCACTTGCCACCACAACACTGTTCTCCTTTTTCAACTGTAGAGAATCTCT ACTGTAGTGTCCCTGCCACTTGCCACCACAACTCTGTTCTCCTTTTTCAACTGTAGAGAATCTCT A T CABYR Ensembl:ENSG00000154040 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs997625705 Functional Loss SNV dbSNP153 33..33 33 - - - 10829 RMVar_ID_10829 Human_SNP_ID_640840920 A-to-I Human chr18 - 24319973 24319973 24319973 ATTAAATTTTTTTTTTTTTTTTTTGTAGAGATAAGGTCTCACTGTATTACCCCGGCGAGTCTTAA ATTAAATTTTTTTTTTTTTTTTTTGTAGAGATGAGGTCTCACTGTATTACCCCGGCGAGTCTTAA T C OSBPL1A Ensembl:ENSG00000141447 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1304688444 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93897,RMVar_hsa_circ_189284,RMVar_hsa_circ_16773,RMVar_hsa_circ_348489,RMVar_hsa_circ_340410,RMVar_hsa_circ_52837,RMVar_hsa_circ_50235,RMVar_hsa_circ_189286,RMVar_hsa_circ_303778,RMVar_hsa_circ_300685,RMVar_hsa_circ_312310,RMVar_hsa_circ_344010,RMVar_hsa_circ_308362,RMVar_hsa_circ_189293,RMVar_hsa_circ_189292,RMVar_hsa_circ_309094,RMVar_hsa_circ_343775,RMVar_hsa_circ_367810,RMVar_hsa_circ_336449,RMVar_hsa_circ_55684,RMVar_hsa_circ_101779,RMVar_hsa_circ_189294,RMVar_hsa_circ_189296,RMVar_hsa_circ_189295,RMVar_hsa_circ_91029,RMVar_hsa_circ_45015,RMVar_hsa_circ_320987,RMVar_hsa_circ_189300,RMVar_hsa_circ_189301 10830 RMVar_ID_10830 Human_SNP_ID_640847627 A-to-I Human chr18 - 24347411 24347411 24347411 AGAGGCCAAGACGGGCGGATCGCCTGAGGTCAAGAGTTCAAGACCAGCCTGGCCAACATGGTGAA AGAGGCCAAGACGGGCGGATCGCCTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGGTGAA T C OSBPL1A Ensembl:ENSG00000141447 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs576807452 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_52837,RMVar_hsa_circ_312310,RMVar_hsa_circ_344010,RMVar_hsa_circ_189293,RMVar_hsa_circ_343775,RMVar_hsa_circ_367810,RMVar_hsa_circ_189294,RMVar_hsa_circ_189305,RMVar_hsa_circ_189303,RMVar_hsa_circ_315543,RMVar_hsa_circ_281292,RMVar_hsa_circ_189302,RMVar_hsa_circ_315969,RMVar_hsa_circ_189306,RMVar_hsa_circ_189304 10831 RMVar_ID_10831 Human_SNP_ID_640851701 A-to-I Human chr18 - 24363773 24363773 24363773 GCCTGGTGTGGTGGTGTGCATCTGTAGTCCCAACTGCTCGGGAGGCTGAGGTTGGAGGATCACTT GCCTGGTGTGGTGGTGTGCATCTGTAGTCCCAGCTGCTCGGGAGGCTGAGGTTGGAGGATCACTT T C OSBPL1A Ensembl:ENSG00000141447 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1361792495 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_52837,RMVar_hsa_circ_312310,RMVar_hsa_circ_344010,RMVar_hsa_circ_189293,RMVar_hsa_circ_343775,RMVar_hsa_circ_367810,RMVar_hsa_circ_189294,RMVar_hsa_circ_189305,RMVar_hsa_circ_189303,RMVar_hsa_circ_315543,RMVar_hsa_circ_281292,RMVar_hsa_circ_189302,RMVar_hsa_circ_315969,RMVar_hsa_circ_189306,RMVar_hsa_circ_189304 10832 RMVar_ID_10832 Human_SNP_ID_640851968 A-to-I Human chr18 - 24364937 24364937 24364937 ACAGTCTCAGCTCACTGCAGCCTCCGCCTCCCAGGCTCAGGTGATCTTCCCCTCTCAGCCTCCTG ACAGTCTCAGCTCACTGCAGCCTCCGCCTCCCGGGCTCAGGTGATCTTCCCCTCTCAGCCTCCTG T C OSBPL1A Ensembl:ENSG00000141447 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1268526841 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_52837,RMVar_hsa_circ_312310,RMVar_hsa_circ_344010,RMVar_hsa_circ_189293,RMVar_hsa_circ_343775,RMVar_hsa_circ_367810,RMVar_hsa_circ_189294,RMVar_hsa_circ_189305,RMVar_hsa_circ_189303,RMVar_hsa_circ_315543,RMVar_hsa_circ_281292,RMVar_hsa_circ_189302,RMVar_hsa_circ_315969,RMVar_hsa_circ_189306,RMVar_hsa_circ_189304 10833 RMVar_ID_10833 Human_SNP_ID_640852148 A-to-I Human chr18 - 24365535 24365535 24365535 CTGTCGCCCAGGTTGGAGTGCAGTGGTGTGATATTGATTCACTGCAACTTCTGTCTCCCGGGTTC CTGTCGCCCAGGTTGGAGTGCAGTGGTGTGATGTTGATTCACTGCAACTTCTGTCTCCCGGGTTC T C OSBPL1A Ensembl:ENSG00000141447 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs891586303 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_52837,RMVar_hsa_circ_312310,RMVar_hsa_circ_344010,RMVar_hsa_circ_189293,RMVar_hsa_circ_343775,RMVar_hsa_circ_367810,RMVar_hsa_circ_189294,RMVar_hsa_circ_189305,RMVar_hsa_circ_189303,RMVar_hsa_circ_315543,RMVar_hsa_circ_281292,RMVar_hsa_circ_189302,RMVar_hsa_circ_315969,RMVar_hsa_circ_189306,RMVar_hsa_circ_189304 10834 RMVar_ID_10834 Human_SNP_ID_641052737 A-to-I Human chr18 - 25203420 25203420 25203420 TGGAGATGGGGTCTTGCTACCTTGCCCAGACTAGTCTTGAACTCCTGGATTCAAGTGATCCTCTC TGGAGATGGGGTCTTGCTACCTTGCCCAGACTTGTCTTGAACTCCTGGATTCAAGTGATCCTCTC T A ZNF521 Ensembl:ENSG00000198795 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1301016816 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 10835 RMVar_ID_10835 Human_SNP_ID_641080940 A-to-I Human chr18 - 25320450 25320450 25320450 AGTTAGCCTTTAGGCCAGGCGCGGTGGCTCACACCTGTAATCCTAGCACTTTGGGAGGCCGAGGC AGTTAGCCTTTAGGCCAGGCGCGGTGGCTCACGCCTGTAATCCTAGCACTTTGGGAGGCCGAGGC T C ZNF521 Ensembl:ENSG00000198795 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1046416640 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_189320,RMVar_hsa_circ_375795,RMVar_hsa_circ_326305,RMVar_hsa_circ_297707 10836 RMVar_ID_10836 Human_SNP_ID_641251511 A-to-I Human chr18 - 26035665 26035663 26035665 GAGCCCAAAACAATCAAAATAATTTCCTTACAAATATTTAAAATGTATAACCATGACTTGCCATT GAGCCCAAAACAATCAAAATAATTTCCTTACA__TATTTAAAATGTATAACCATGACTTGCCATT ATT A SS18 Ensembl:ENSG00000141380 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1436534400 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_1873931,Human_RBP_ID_21929396 RMVar_hsa_circ_22229,RMVar_hsa_circ_189334,RMVar_hsa_circ_105052,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 10837 RMVar_ID_10837 Human_SNP_ID_641256472 A-to-I Human chr18 - 26055319 26055319 26055319 GGGATTACAGGCGCACACCACCACACCTGGCTAATTTTCGTATTTTTAATAGAGATGGGGTTTCA GGGATTACAGGCGCACACCACCACACCTGGCTTATTTTCGTATTTTTAATAGAGATGGGGTTTCA T A SS18 Ensembl:ENSG00000141380 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs563524899 Functional Loss SNV dbSNP153 33..33 33 - - - 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_189349,RMVar_hsa_circ_189350,RMVar_hsa_circ_189348 10838 RMVar_ID_10838 Human_SNP_ID_641262471 A-to-I Human chr18 - 26078843 26078843 26078843 TCACTCTGTTGCCCAGGCTGGAGTGCAGTGGCATGATCTCGGCTCACTGCAACCTTTGCCTCCTG TCACTCTGTTGCCCAGGCTGGAGTGCAGTGGCGTGATCTCGGCTCACTGCAACCTTTGCCTCCTG T C SS18 Ensembl:ENSG00000141380 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903105014 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_321444,RMVar_hsa_circ_59866,RMVar_hsa_circ_75773,RMVar_hsa_circ_189339,RMVar_hsa_circ_304018,RMVar_hsa_circ_189346,RMVar_hsa_circ_346518,RMVar_hsa_circ_5770,RMVar_hsa_circ_189347,RMVar_hsa_circ_272775,RMVar_hsa_circ_347741,RMVar_hsa_circ_63002,RMVar_hsa_circ_299711,RMVar_hsa_circ_189348,RMVar_hsa_circ_317532,RMVar_hsa_circ_189353,RMVar_hsa_circ_344961,RMVar_hsa_circ_328733,RMVar_hsa_circ_337570,RMVar_hsa_circ_54904 10839 RMVar_ID_10839 Human_SNP_ID_641263283 A-to-I Human chr18 - 26081975 26081975 26081975 TGGCTCACTGCAGCCTCAACCTCCTGTTCTCAAGTGATCCTCCCACCTTAGCCTCCTAAGTAGCA TGGCTCACTGCAGCCTCAACCTCCTGTTCTCAGGTGATCCTCCCACCTTAGCCTCCTAAGTAGCA T C SS18 Ensembl:ENSG00000141380 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs897990219 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_321444,RMVar_hsa_circ_59866,RMVar_hsa_circ_75773,RMVar_hsa_circ_189339,RMVar_hsa_circ_304018,RMVar_hsa_circ_189346,RMVar_hsa_circ_346518,RMVar_hsa_circ_5770,RMVar_hsa_circ_189347,RMVar_hsa_circ_272775,RMVar_hsa_circ_347741,RMVar_hsa_circ_63002,RMVar_hsa_circ_299711,RMVar_hsa_circ_189348,RMVar_hsa_circ_317532,RMVar_hsa_circ_189353,RMVar_hsa_circ_344961,RMVar_hsa_circ_328733,RMVar_hsa_circ_337570 10840 RMVar_ID_10840 Human_SNP_ID_641283015 A-to-I Human chr18 - 26169240 26169240 26169240 AAACTAGCCAGGCACAGTGGCTCACGCCTGTAATCCCAGCGCTTTGGGAGGCTAAGGCAGGCAGA AAACTAGCCAGGCACAGTGGCTCACGCCTGTATTCCCAGCGCTTTGGGAGGCTAAGGCAGGCAGA T A lnc-SS18-8 RNACentral:URS0000D57798 lincRNA intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1207103491 Functional Loss SNV dbSNP153 33..33 33 - - - 10841 RMVar_ID_10841 Human_SNP_ID_641283076 A-to-I Human chr18 - 26169605 26169605 26169605 GAACTCGTGACCGCAAGCGATTCACCCACCTCAGCCTCCCAAAGTGCTGGGATTACCGGCTTGAG GAACTCGTGACCGCAAGCGATTCACCCACCTCGGCCTCCCAAAGTGCTGGGATTACCGGCTTGAG T C lnc-SS18-8 RNACentral:URS0000D57798 lincRNA intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1351672611 Functional Loss SNV dbSNP153 33..33 33 - - - 10842 RMVar_ID_10842 Human_SNP_ID_641283093 A-to-I Human chr18 - 26169690 26169690 26169690 GGTGCGCGCCACCACGCCCGGCTAATTTTTGTATTTTGTATTTTTGGTAGAGATGGGGTTTCGCC GGTGCGCGCCACCACGCCCGGCTAATTTTTGTGTTTTGTATTTTTGGTAGAGATGGGGTTTCGCC T C lnc-SS18-8 RNACentral:URS0000D57798 lincRNA intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1403818697 Functional Loss SNV dbSNP153 33..33 33 - - - 10843 RMVar_ID_10843 Human_SNP_ID_641283107 A-to-I Human chr18 - 26169769 26169769 26169769 TGACCTCGGCTTACTGCAACCTCCGCCTTCCCAGATTCAAGCGATTCTCCTGCCTCAGGCTCCCA TGACCTCGGCTTACTGCAACCTCCGCCTTCCCGGATTCAAGCGATTCTCCTGCCTCAGGCTCCCA T C lnc-SS18-8 RNACentral:URS0000D57798 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1161083095 Functional Loss SNV dbSNP153 33..33 33 - - - 10844 RMVar_ID_10844 Human_SNP_ID_641283108 A-to-I Human chr18 - 26169769 26169769 26169769 TGACCTCGGCTTACTGCAACCTCCGCCTTCCCAGATTCAAGCGATTCTCCTGCCTCAGGCTCCCA TGACCTCGGCTTACTGCAACCTCCGCCTTCCCCGATTCAAGCGATTCTCCTGCCTCAGGCTCCCA T G lnc-SS18-8 RNACentral:URS0000D57798 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1161083095 Functional Loss SNV dbSNP153 33..33 33 - - - 10845 RMVar_ID_10845 Human_SNP_ID_641303221 A-to-I Human chr18 + 26249868 26249868 26249868 CCCCAGCCTCCTAAGTAGCTGGGATTACAGGCACATGCCACCATGCCCGGCTAATTTTTGAATTT CCCCAGCCTCCTAAGTAGCTGGGATTACAGGCGCATGCCACCATGCCCGGCTAATTTTTGAATTT A G TAF4B Ensembl:ENSG00000141384 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs915240414 Functional Loss SNV dbSNP153 33..33 33 - - - 10846 RMVar_ID_10846 Human_SNP_ID_641308050 A-to-I Human chr18 + 26269069 26269069 26269069 TGGTCTCGAACTCTTGACCAAGTAATCCGCCTACCTCAGCCTCCCAAAGTCCTGGGATTACAGGC TGGTCTCGAACTCTTGACCAAGTAATCCGCCTGCCTCAGCCTCCCAAAGTCCTGGGATTACAGGC A G TAF4B Ensembl:ENSG00000141384 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs943965686 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27391,RMVar_hsa_circ_348037,RMVar_hsa_circ_51575,RMVar_hsa_circ_274146,RMVar_hsa_circ_35878,RMVar_hsa_circ_22577,RMVar_hsa_circ_51553,RMVar_hsa_circ_189356,RMVar_hsa_circ_58463,RMVar_hsa_circ_43706 10847 RMVar_ID_10847 Human_SNP_ID_641331100 A-to-I Human chr18 + 26359918 26359918 26359918 TTTTTTTTTTTTGGTAGAGACGGAGTTTTGCCATGTTGCCCAGCTTGGTCTCGAACTTCTGAGCT TTTTTTTTTTTTGGTAGAGACGGAGTTTTGCCGTGTTGCCCAGCTTGGTCTCGAACTTCTGAGCT A G TAF4B Ensembl:ENSG00000141384 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1178644454 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8470068 10848 RMVar_ID_10848 Human_SNP_ID_641331466 A-to-I Human chr18 + 26361484 26361484 26361484 TATGGAAAAACTGGCCAGGCATGATGGCTCACACCTGTAATCCCAGCACATTGGGAGGCTGAGGT TATGGAAAAACTGGCCAGGCATGATGGCTCACTCCTGTAATCCCAGCACATTGGGAGGCTGAGGT A T TAF4B Ensembl:ENSG00000141384 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348598015 Functional Loss SNV dbSNP153 33..33 33 - - - 10849 RMVar_ID_10849 Human_SNP_ID_641333662 A-to-I Human chr18 + 26371222 26371222 26371222 CTAAATTCTACTGAATCGACACATATTTATAAAAAGTGTTAGATGACAATAAGTCTGTTTAAACA CTAAATTCTACTGAATCGACACATATTTATAAGAAGTGTTAGATGACAATAAGTCTGTTTAAACA A G TAF4B Ensembl:ENSG00000141384 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1258498552 Functional Loss SNV dbSNP153 33..33 33 - - - 10850 RMVar_ID_10850 Human_SNP_ID_641335775 A-to-I Human chr18 + 26381038 26381037 26381039 TCTTATTTATATACCTACTTATCTTTTGAGACAGAGTCTTGCCCTGTCGCCCAGGCTGGAGTGCA TCTTATTTATATACCTACTTATCTTTTGAGAC__AGTCTTGCCCTGTCGCCCAGGCTGGAGTGCA CAG C TAF4B Ensembl:ENSG00000141384 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs372146460 Functional Loss DEL dbSNP153 33..34 33 - - - 10851 RMVar_ID_10851 Human_SNP_ID_641386145 A-to-I Human chr18 - 26599369 26599369 26599369 GCAGTGCAGTACTGACAGACCTAAAAACTGCTAGCCAAAAGAGAATCAAGACTGCCACCTGGGCT GCAGTGCAGTACTGACAGACCTAAAAACTGCTGGCCAAAAGAGAATCAAGACTGCCACCTGGGCT T C KCTD1 Ensembl:ENSG00000134504 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1395559512 Functional Loss SNV dbSNP153 33..33 33 - - - 10852 RMVar_ID_10852 Human_SNP_ID_641386206 A-to-I Human chr18 + 26599691 26599691 26599691 GATCCTTCGGCCTGGTGGATGTCTTTTTCTGAAAGAGCCAGTAGAGACAGCTGTAGATAACAATA GATCCTTCGGCCTGGTGGATGTCTTTTTCTGAGAGAGCCAGTAGAGACAGCTGTAGATAACAATA A G CIAPIN1P Ensembl:ENSG00000263846 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs535693924 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5583343 10853 RMVar_ID_10853 Human_SNP_ID_641441183 A-to-I Human chr18 - 26832262 26832262 26832262 TATGCTGCCCTCAGCCCTGGACCAACTCAGCCAACTTAACATTACCTATCCCATGCTGTTCAAAC TATGCTGCCCTCAGCCCTGGACCAACTCAGCCGACTTAACATTACCTATCCCATGCTGTTCAAAC T C AC018371.2 Ensembl:ENSG00000266184 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878937893 Functional Loss SNV dbSNP153 33..33 33 - - - 10854 RMVar_ID_10854 Human_SNP_ID_641441187 A-to-I Human chr18 - 26832282 26832282 26832282 GAGAAAGGAGGGAAGATAATTATGCTGCCCTCAGCCCTGGACCAACTCAGCCAACTTAACATTAC GAGAAAGGAGGGAAGATAATTATGCTGCCCTCGGCCCTGGACCAACTCAGCCAACTTAACATTAC T C AC018371.2 Ensembl:ENSG00000266184 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1273742416 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5583407 Human_miRNA_ID_1825628,Human_miRNA_ID_1825791 10855 RMVar_ID_10855 Human_SNP_ID_641441195 A-to-I Human chr18 - 26832325 26832325 26832325 CTCTGTGTCCACGCTAGCAGGGCCTAATGACAAGTCAGATGTGGAGAAAGGAGGGAAGATAATTA CTCTGTGTCCACGCTAGCAGGGCCTAATGACAGGTCAGATGTGGAGAAAGGAGGGAAGATAATTA T C AC018371.2 Ensembl:ENSG00000266184 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs972762542 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4495242,Human_RBP_ID_5583407 10856 RMVar_ID_10856 Human_SNP_ID_641755942 A-to-I Human chr18 - 28171170 28171170 28171170 CTGGAGTGCAGTGGCACAGTCTTGGCTCAACTACATCCTCCGTCTCCCGGGCTCAAGGAATTCTC CTGGAGTGCAGTGGCACAGTCTTGGCTCAACTTCATCCTCCGTCTCCCGGGCTCAAGGAATTCTC T A CDH2 Ensembl:ENSG00000170558 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1414146794 Functional Loss SNV dbSNP153 33..33 33 - - - 10857 RMVar_ID_10857 Human_SNP_ID_208459983 A-to-I Human chr4 + 150245438 150245438 150245438 ATGTGCCCAACGTGCAGGTTTGTTACATATGTATACATGCGTCATGCTGGTGTGCTGCACTCATT ATGTGCCCAACGTGCAGGTTTGTTACATATGTGTACATGCGTCATGCTGGTGTGCTGCACTCATT A G DCLK2 Ensembl:ENSG00000170390 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs778960423 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_378027,RMVar_hsa_circ_18164,RMVar_hsa_circ_35991,RMVar_hsa_circ_43373 10858 RMVar_ID_10858 Human_SNP_ID_208463928 A-to-I Human chr4 + 150254845 150254845 150254845 AGGACTACAGGTGCACGCCACCTTGCCCGGCTAATTTTTAAATTCTTTGTGGAGATGGAGTCTCT AGGACTACAGGTGCACGCCACCTTGCCCGGCTGATTTTTAAATTCTTTGTGGAGATGGAGTCTCT A G DCLK2 Ensembl:ENSG00000170390 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1259231627 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15069838 10859 RMVar_ID_10859 Human_SNP_ID_208591921 A-to-I Human chr4 - 150786651 150786651 150786651 AGTTTGGGGATAAAATCATTGGATGGTGGAAAATGGTCCTCTTTTGCTGAGTCCACTTCTGGGTG AGTTTGGGGATAAAATCATTGGATGGTGGAAAGTGGTCCTCTTTTGCTGAGTCCACTTCTGGGTG T C LRBA Ensembl:ENSG00000198589 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042104075 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_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_229039,RMVar_hsa_circ_86468,RMVar_hsa_circ_267994,RMVar_hsa_circ_115571,RMVar_hsa_circ_292355,RMVar_hsa_circ_353167,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_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_229052,RMVar_hsa_circ_229050,RMVar_hsa_circ_229047,RMVar_hsa_circ_229048,RMVar_hsa_circ_229046,RMVar_hsa_circ_31786,RMVar_hsa_circ_284696,RMVar_hsa_circ_229043,RMVar_hsa_circ_229044,RMVar_hsa_circ_312203,RMVar_hsa_circ_370042,RMVar_hsa_circ_370686,RMVar_hsa_circ_362207,RMVar_hsa_circ_303562,RMVar_hsa_circ_275845,RMVar_hsa_circ_277075,RMVar_hsa_circ_45412,RMVar_hsa_circ_229056,RMVar_hsa_circ_229058,RMVar_hsa_circ_229059,RMVar_hsa_circ_229057,RMVar_hsa_circ_229055 10860 RMVar_ID_10860 Human_SNP_ID_208646431 A-to-I Human chr4 - 151007418 151007418 151007418 TCACTGAAAGCTCCGCCTCCCGGGTTCACACTATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGA TCACTGAAAGCTCCGCCTCCCGGGTTCACACTGTTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGA T C LRBA Ensembl:ENSG00000198589 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs540233673 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25786636 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 10861 RMVar_ID_10861 Human_SNP_ID_208670768 A-to-I Human chr4 + 151103264 151103261 151103265 ACTCAGTAAATATGATTATTATTACTATTATTATTTGAGTCAGAGTCTTGCTCTGTTGCCCAGGC ACTCAGTAAATATGATTATTATTACTATTA____TTGAGTCAGAGTCTTGCTCTGTTGCCCAGGC ATTAT A RPS3A Ensembl:ENSG00000145425 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1187689351 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_214000,Human_RBP_ID_15072819,Human_RBP_ID_17574873,Human_RBP_ID_22288602,Human_RBP_ID_25786713 10862 RMVar_ID_10862 Human_SNP_ID_208670770 A-to-I Human chr4 + 151103269 151103269 151103269 GTAAATATGATTATTATTACTATTATTATTTGAGTCAGAGTCTTGCTCTGTTGCCCAGGCTCGAG GTAAATATGATTATTATTACTATTATTATTTGCGTCAGAGTCTTGCTCTGTTGCCCAGGCTCGAG A C RPS3A Ensembl:ENSG00000145425 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1001359684 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_214000,Human_RBP_ID_15072819,Human_RBP_ID_17574873,Human_RBP_ID_17627859 10863 RMVar_ID_10863 Human_SNP_ID_208671528 A-to-I Human chr4 + 151105468 151105468 151105468 CCAGCTTCTCGGGAGGCTGAGGCATGAAAATCACTTGAACCTGGGAGGTGGAGGTTGCAGTGAGC CCAGCTTCTCGGGAGGCTGAGGCATGAAAATCCCTTGAACCTGGGAGGTGGAGGTTGCAGTGAGC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs987278521 Functional Loss SNV dbSNP153 33..33 33 - - - 10864 RMVar_ID_10864 Human_SNP_ID_208671644 A-to-I Human chr4 + 151105832 151105832 151105832 CTTGTGTCTCAGCCTCCCCAGTAGCTAGGATTATAGGCACCCACCACCATGCTGGGCTAATTTTT CTTGTGTCTCAGCCTCCCCAGTAGCTAGGATTGTAGGCACCCACCACCATGCTGGGCTAATTTTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs570367351 Functional Loss SNV dbSNP153 33..33 33 - - - 10865 RMVar_ID_10865 Human_SNP_ID_208671654 A-to-I Human chr4 + 151105858 151105858 151105858 AGGATTATAGGCACCCACCACCATGCTGGGCTAATTTTTGCATTTTTTAGTGGAGATGGGGGTTT AGGATTATAGGCACCCACCACCATGCTGGGCTGATTTTTGCATTTTTTAGTGGAGATGGGGGTTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1036093665 Functional Loss SNV dbSNP153 33..33 33 - - - 10866 RMVar_ID_10866 Human_SNP_ID_208671675 A-to-I Human chr4 + 151105929 151105929 151105929 GTTGGCAAGGCTTGTCTTGAATTCCTGGCCTCAAGTGATCCTCCCGCCTTGGCCTCCCAAATTGC GTTGGCAAGGCTTGTCTTGAATTCCTGGCCTCCAGTGATCCTCCCGCCTTGGCCTCCCAAATTGC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1469903265 Functional Loss SNV dbSNP153 33..33 33 - - - 10867 RMVar_ID_10867 Human_SNP_ID_208672715 A-to-I Human chr4 + 151109489 151109489 151109489 CTCTTGTCGCCTAGACTGGAGCGCAATGGCGCAATCTCAGCCCACTGCAACCTCTGCCTCCCAGG CTCTTGTCGCCTAGACTGGAGCGCAATGGCGCCATCTCAGCCCACTGCAACCTCTGCCTCCCAGG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1266960885 Functional Loss SNV dbSNP153 33..33 33 - - - 10868 RMVar_ID_10868 Human_SNP_ID_208674011 A-to-I Human chr4 + 151115669 151115669 151115669 CACCATTGCACTCCAGCCTGGGTTGACGAGCGAAACTCCATCTCAAAAATAAAAATACAGATACA CACCATTGCACTCCAGCCTGGGTTGACGAGCGGAACTCCATCTCAAAAATAAAAATACAGATACA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1002347304 Functional Loss SNV dbSNP153 33..33 33 - - - 10869 RMVar_ID_10869 Human_SNP_ID_208676261 A-to-I Human chr4 + 151124509 151124509 151124509 GGGAGGCCAAGGCAGGTGGATTTTCTGAGCTCAGGAGTTCAAGACCAGCCCGGCAACACAGTGAA GGGAGGCCAAGGCAGGTGGATTTTCTGAGCTCGGGAGTTCAAGACCAGCCCGGCAACACAGTGAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1259295884 Functional Loss SNV dbSNP153 33..33 33 - - - 10870 RMVar_ID_10870 Human_SNP_ID_208676307 A-to-I Human chr4 - 151124717 151124717 151124717 ATAGATAAAACTAATTTTTTTTTTTTTAGAGAAGGAGTCTTGTTCTGCTGCCCAGGCTGGAGTGC ATAGATAAAACTAATTTTTTTTTTTTTAGAGAGGGAGTCTTGTTCTGCTGCCCAGGCTGGAGTGC T C SH3D19 Ensembl:ENSG00000109686 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1434908245 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_229133,RMVar_hsa_circ_120125,RMVar_hsa_circ_77723,RMVar_hsa_circ_229132 10871 RMVar_ID_10871 Human_SNP_ID_208685930 A-to-I Human chr4 - 151165296 151165296 151165296 GCTCTCTCACCCAGGCTGGAGTGCAGTGGCACAATCTCAGCTCACTGCACCCTCTGCCTCCCGGA GCTCTCTCACCCAGGCTGGAGTGCAGTGGCACTATCTCAGCTCACTGCACCCTCTGCCTCCCGGA T A SH3D19 Ensembl:ENSG00000109686 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs919603946 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_229133,RMVar_hsa_circ_120125,RMVar_hsa_circ_351514,RMVar_hsa_circ_28687,RMVar_hsa_circ_71263,RMVar_hsa_circ_359458,RMVar_hsa_circ_347761,RMVar_hsa_circ_55424,RMVar_hsa_circ_357810,RMVar_hsa_circ_366899,RMVar_hsa_circ_356172,RMVar_hsa_circ_22006,RMVar_hsa_circ_64392,RMVar_hsa_circ_350295,RMVar_hsa_circ_361606,RMVar_hsa_circ_120300,RMVar_hsa_circ_229137,RMVar_hsa_circ_229138,RMVar_hsa_circ_354465,RMVar_hsa_circ_77739,RMVar_hsa_circ_229139,RMVar_hsa_circ_229140 10872 RMVar_ID_10872 Human_SNP_ID_208690521 A-to-I Human chr4 - 151185902 151185902 151185902 TTGAGTAGCTGGGATTACAGGCACCCACCACCATGCCCGGCTAATTTTTGTATTTTTAGTAGAGA TTGAGTAGCTGGGATTACAGGCACCCACCACCGTGCCCGGCTAATTTTTGTATTTTTAGTAGAGA T C SH3D19 Ensembl:ENSG00000109686 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1184979260 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_229133,RMVar_hsa_circ_120125,RMVar_hsa_circ_28687,RMVar_hsa_circ_55424,RMVar_hsa_circ_354465,RMVar_hsa_circ_229141,RMVar_hsa_circ_61638,RMVar_hsa_circ_357366,RMVar_hsa_circ_57633,RMVar_hsa_circ_286732 10873 RMVar_ID_10873 Human_SNP_ID_208690524 A-to-I Human chr4 - 151185908 151185908 151185908 AGCCTCTTGAGTAGCTGGGATTACAGGCACCCACCACCATGCCCGGCTAATTTTTGTATTTTTAG AGCCTCTTGAGTAGCTGGGATTACAGGCACCCCCCACCATGCCCGGCTAATTTTTGTATTTTTAG T G SH3D19 Ensembl:ENSG00000109686 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1561302879 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_229133,RMVar_hsa_circ_120125,RMVar_hsa_circ_28687,RMVar_hsa_circ_55424,RMVar_hsa_circ_354465,RMVar_hsa_circ_229141,RMVar_hsa_circ_61638,RMVar_hsa_circ_357366,RMVar_hsa_circ_57633,RMVar_hsa_circ_286732 10874 RMVar_ID_10874 Human_SNP_ID_208708265 A-to-I Human chr4 - 151257833 151257833 151257833 ATGATCGTAGCATACTGCAGCCTAGACCTCCCAGGCTCAAGCGATCCTCCCTCCTCAGTCTCTGG ATGATCGTAGCATACTGCAGCCTAGACCTCCCGGGCTCAAGCGATCCTCCCTCCTCAGTCTCTGG T C SH3D19 Ensembl:ENSG00000109686 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041314408 Functional Loss SNV dbSNP153 33..33 33 - - - 10875 RMVar_ID_10875 Human_SNP_ID_208708280 A-to-I Human chr4 - 151257896 151257896 151257896 TGGTTGCTTTTTTTATTTTTAGACAGACTCTCACTCTCTTACCTAGGCTAGAAGTACAGTGGCAT TGGTTGCTTTTTTTATTTTTAGACAGACTCTCCCTCTCTTACCTAGGCTAGAAGTACAGTGGCAT T G SH3D19 Ensembl:ENSG00000109686 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005957990 Functional Loss SNV dbSNP153 33..33 33 - - - 10876 RMVar_ID_10876 Human_SNP_ID_208713150 A-to-I Human chr4 - 151278361 151278361 151278361 AGGGAGGCTGAGTGGGAGGATTGCTTGAACCCAGGAGTCTGAGGTTGCAGTGGGCTATGATTGCA AGGGAGGCTGAGTGGGAGGATTGCTTGAACCCGGGAGTCTGAGGTTGCAGTGGGCTATGATTGCA T C SH3D19 Ensembl:ENSG00000109686 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1401479582 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15073881 10877 RMVar_ID_10877 Human_SNP_ID_208720584 A-to-I Human chr4 - 151309890 151309890 151309890 GACCTCCCGGGCTCAAGAAATCCTCCCACCTCAGCCTTCCAGGTAGCTGGGACTACAAGTATGTG GACCTCCCGGGCTCAAGAAATCCTCCCACCTCCGCCTTCCAGGTAGCTGGGACTACAAGTATGTG T G SH3D19 Ensembl:ENSG00000109686 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1385498374 Functional Loss SNV dbSNP153 33..33 33 - - - 10878 RMVar_ID_10878 Human_SNP_ID_208729552 A-to-I Human chr4 - 151348867 151348867 151348867 TGTTTCACTCTTCTTGCCCACACTGGAGTGCAATGGTGCAATCTCAGCTTACTGCAACCTCCACC TGTTTCACTCTTCTTGCCCACACTGGAGTGCAGTGGTGCAATCTCAGCTTACTGCAACCTCCACC T C AC104819.3 Ensembl:ENSG00000270265 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs745454935 Functional Loss SNV dbSNP153 33..33 33 - - - 10879 RMVar_ID_10879 Human_SNP_ID_208742920 A-to-I Human chr4 - 151405033 151405033 151405033 TAAAAATACAACAATTAGCTGGGCGTGTTGGCAGGCGCCTGTAATCCCAGCCACTCGTGAGTCTG TAAAAATACAACAATTAGCTGGGCGTGTTGGCTGGCGCCTGTAATCCCAGCCACTCGTGAGTCTG T A FAM160A1-DT,FAM160A1-DT:2,FAM160A1-DT:3,FAM160A1-DT:4 RNACentral:URS0000D5A786,RNACentral:URS0000D5DBA5,RNACentral:URS0000D5DFDC,RNACentral:URS0000D5B5C9 lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs906243838 Functional Loss SNV dbSNP153 33..33 33 - - - 10880 RMVar_ID_10880 Human_SNP_ID_208742959 A-to-I Human chr4 - 151405171 151405171 151405171 TATTAATAATGATTATCTCAGCCAGGCATGGTAGCTTATGCCTGTAATCCCAGAACTTTGGGAGG TATTAATAATGATTATCTCAGCCAGGCATGGTGGCTTATGCCTGTAATCCCAGAACTTTGGGAGG T C FAM160A1-DT,FAM160A1-DT:2,FAM160A1-DT:3,FAM160A1-DT:4 RNACentral:URS0000D5A786,RNACentral:URS0000D5DBA5,RNACentral:URS0000D5DFDC,RNACentral:URS0000D5B5C9 lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1361738486 Functional Loss SNV dbSNP153 33..33 33 - - - 10881 RMVar_ID_10881 Human_SNP_ID_208743024 A-to-I Human chr4 - 151405437 151405437 151405437 AAGGATAAGCAGATGTGGTGGTACGGGCCTATAGTCCCAACTGCTTAGGAGGCTGAGGCAGAAGG AAGGATAAGCAGATGTGGTGGTACGGGCCTATGGTCCCAACTGCTTAGGAGGCTGAGGCAGAAGG T C FAM160A1-DT,FAM160A1-DT:2,FAM160A1-DT:3,FAM160A1-DT:4 RNACentral:URS0000D5A786,RNACentral:URS0000D5DBA5,RNACentral:URS0000D5DFDC,RNACentral:URS0000D5B5C9 lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1427307948 Functional Loss SNV dbSNP153 33..33 33 - - - 10882 RMVar_ID_10882 Human_SNP_ID_208754840 A-to-I Human chr4 + 151456086 151456086 151456086 AACATACATCATCTATGGAAAAAAAAGCTGTTAAGGCACCAAAAAAAACCCACTGTAGGACTGTA AACATACATCATCTATGGAAAAAAAAGCTGTTGAGGCACCAAAAAAAACCCACTGTAGGACTGTA A G FAM160A1 Ensembl:ENSG00000164142 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924105056 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58110,RMVar_hsa_circ_229144,RMVar_hsa_circ_361940,RMVar_hsa_circ_320247,RMVar_hsa_circ_229145 10883 RMVar_ID_10883 Human_SNP_ID_208754857 A-to-I Human chr4 + 151456170 151456170 151456170 GAGATTTATTGACATGATAAAATTAAACAACCATAACTCTCTAATTTATTAGAAAATCTCCATCA GAGATTTATTGACATGATAAAATTAAACAACCGTAACTCTCTAATTTATTAGAAAATCTCCATCA A G FAM160A1 Ensembl:ENSG00000164142 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1443584154 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58110,RMVar_hsa_circ_229144,RMVar_hsa_circ_361940,RMVar_hsa_circ_320247,RMVar_hsa_circ_229145 10884 RMVar_ID_10884 Human_SNP_ID_208754881 A-to-I Human chr4 + 151456248 151456247 151456248 CCGAAAGTCTATCCATTGAAAAGGTTCTTTTTAAAATAACATCAGCTTTCAGTACTCTAAAATGA CCGAAAGTCTATCCATTGAAAAGGTTCTTTTT_AAATAACATCAGCTTTCAGTACTCTAAAATGA TA T FAM160A1 Ensembl:ENSG00000164142 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1561503202 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_58110,RMVar_hsa_circ_229144,RMVar_hsa_circ_361940,RMVar_hsa_circ_320247,RMVar_hsa_circ_229145 10885 RMVar_ID_10885 Human_SNP_ID_208996403 A-to-I Human chr4 - 152473132 152473132 152473132 TCATGCTATCTTCCCACCTCAGCCTCCTGAGTAGCTGGGACTACAGGTGTACATCACCACACCCA TCATGCTATCTTCCCACCTCAGCCTCCTGAGTTGCTGGGACTACAGGTGTACATCACCACACCCA T A FBXW7 Ensembl:ENSG00000109670 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1377311032 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112966,RMVar_hsa_circ_122878,RMVar_hsa_circ_229166,RMVar_hsa_circ_229167,RMVar_hsa_circ_229168,RMVar_hsa_circ_229169 10886 RMVar_ID_10886 Human_SNP_ID_208996784 A-to-I Human chr4 - 152474804 152474804 152474804 AAAATTAGCTGGGAGTGGTGGCGTGCGCCTGTAGTCCCAGCTACTTGAGAGGCTGAGGCAGGAGA AAAATTAGCTGGGAGTGGTGGCGTGCGCCTGTGGTCCCAGCTACTTGAGAGGCTGAGGCAGGAGA T C FBXW7 Ensembl:ENSG00000109670 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs551797050 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112966,RMVar_hsa_circ_122878,RMVar_hsa_circ_229166,RMVar_hsa_circ_229167,RMVar_hsa_circ_229168,RMVar_hsa_circ_229169 10887 RMVar_ID_10887 Human_SNP_ID_209006839 A-to-I Human chr4 - 152517008 152517008 152517008 GACCAGCTGGACAACATGGCGAAACCATCTCTACTGAACATACAAAAATTAGCTGGGTGTAGTGG GACCAGCTGGACAACATGGCGAAACCATCTCTGCTGAACATACAAAAATTAGCTGGGTGTAGTGG T C FBXW7 Ensembl:ENSG00000109670 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879319683 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15077517 RMVar_hsa_circ_112966,RMVar_hsa_circ_122878,RMVar_hsa_circ_229167,RMVar_hsa_circ_229168 10888 RMVar_ID_10888 Human_SNP_ID_209007131 A-to-I Human chr4 - 152518278 152518278 152518278 TATATAAATAAATAAAATAGTAGGCTGGGTGCAGTGGCTCATGGCTGTAATCCCAGCACATTGGG TATATAAATAAATAAAATAGTAGGCTGGGTGCGGTGGCTCATGGCTGTAATCCCAGCACATTGGG T C FBXW7 Ensembl:ENSG00000109670 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs887971530 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112966,RMVar_hsa_circ_122878,RMVar_hsa_circ_229167,RMVar_hsa_circ_229168 10889 RMVar_ID_10889 Human_SNP_ID_209007148 A-to-I Human chr4 - 152518350 152518350 152518350 TCAAGACTGTAGTGAGCCAAGATCCTGCCACTATACTTTAGCCTGGGTGAGAGAGCAAGACCCTG TCAAGACTGTAGTGAGCCAAGATCCTGCCACTGTACTTTAGCCTGGGTGAGAGAGCAAGACCCTG T C FBXW7 Ensembl:ENSG00000109670 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1029410034 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1387775,Human_RBP_ID_15077540 RMVar_hsa_circ_112966,RMVar_hsa_circ_122878,RMVar_hsa_circ_229167,RMVar_hsa_circ_229168 10890 RMVar_ID_10890 Human_SNP_ID_209032045 A-to-I Human chr4 - 152622853 152622851 152622853 CATCCTGGGTGACAGAGCAAGATTCTGTCTCAAAGAAAAGAAAAAGAAATGGTCCCATTGCTACG CATCCTGGGTGACAGAGCAAGATTCTGTCTCA__GAAAAGAAAAAGAAATGGTCCCATTGCTACG CTT C TMEM154 Ensembl:ENSG00000170006 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1208241388 Functional Loss DEL dbSNP153 33..34 33 - - - 10891 RMVar_ID_10891 Human_SNP_ID_209032081 A-to-I Human chr4 - 152622981 152622981 152622981 AATGCAAAAATTAGCCAGGTGTGGTAGTACACACCTGTAATCCCACCTACTCGGGGGGCTGAGGC AATGCAAAAATTAGCCAGGTGTGGTAGTACACTCCTGTAATCCCACCTACTCGGGGGGCTGAGGC T A TMEM154 Ensembl:ENSG00000170006 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1307434465 Functional Loss SNV dbSNP153 33..33 33 - - - 10892 RMVar_ID_10892 Human_SNP_ID_209032082 A-to-I Human chr4 - 152622981 152622981 152622981 AATGCAAAAATTAGCCAGGTGTGGTAGTACACACCTGTAATCCCACCTACTCGGGGGGCTGAGGC AATGCAAAAATTAGCCAGGTGTGGTAGTACACGCCTGTAATCCCACCTACTCGGGGGGCTGAGGC T C TMEM154 Ensembl:ENSG00000170006 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1307434465 Functional Loss SNV dbSNP153 33..33 33 - - - 10893 RMVar_ID_10893 Human_SNP_ID_209032084 A-to-I Human chr4 - 152622985 152622985 152622985 CAAAAATGCAAAAATTAGCCAGGTGTGGTAGTACACACCTGTAATCCCACCTACTCGGGGGGCTG CAAAAATGCAAAAATTAGCCAGGTGTGGTAGTGCACACCTGTAATCCCACCTACTCGGGGGGCTG T C TMEM154 Ensembl:ENSG00000170006 Protein coding 3'UTR GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,31158229,31158229 RNA-Seq:(High) rs1207488623 Functional Loss SNV dbSNP153 33..33 33 - - - 10894 RMVar_ID_10894 Human_SNP_ID_209032085 A-to-I Human chr4 - 152622988 152622988 152622988 TTACAAAAATGCAAAAATTAGCCAGGTGTGGTAGTACACACCTGTAATCCCACCTACTCGGGGGG TTACAAAAATGCAAAAATTAGCCAGGTGTGGTGGTACACACCTGTAATCCCACCTACTCGGGGGG T C TMEM154 Ensembl:ENSG00000170006 Protein coding 3'UTR GSE38233;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;Bronchiolar epithelium,BERP35T4 cell line - 24183664,31158229 RNA-Seq:(High) rs900666071 Functional Loss SNV dbSNP153 33..33 33 - - - 10895 RMVar_ID_10895 Human_SNP_ID_209032096 A-to-I Human chr4 - 152623029 152623029 152623029 GAGTTTGAGACCAGCCTGGCCAACATGGTGAAACCCCATTTTTACAAAAATGCAAAAATTAGCCA GAGTTTGAGACCAGCCTGGCCAACATGGTGAAGCCCCATTTTTACAAAAATGCAAAAATTAGCCA T C TMEM154 Ensembl:ENSG00000170006 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1052383872 Functional Loss SNV dbSNP153 33..33 33 - - - 10896 RMVar_ID_10896 Human_SNP_ID_209032104 A-to-I Human chr4 - 152623054 152623054 152623054 CGGCTGGTGGATTGCCTGAGCTCGGGAGTTTGAGACCAGCCTGGCCAACATGGTGAAACCCCATT CGGCTGGTGGATTGCCTGAGCTCGGGAGTTTGGGACCAGCCTGGCCAACATGGTGAAACCCCATT T C TMEM154 Ensembl:ENSG00000170006 Protein coding 3'UTR GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,31158229,31158229 RNA-Seq:(High) rs1422006440 Functional Loss SNV dbSNP153 33..33 33 - - - 10897 RMVar_ID_10897 Human_SNP_ID_209032238 A-to-I Human chr4 - 152623683 152623683 152623683 TAGAGACAGGGTTTCGCCATGTTGGCCAAGCTAGTCTCAAACTCCTGGGCTCAAGTGATCCGCCC TAGAGACAGGGTTTCGCCATGTTGGCCAAGCTGGTCTCAAACTCCTGGGCTCAAGTGATCCGCCC T C TMEM154 Ensembl:ENSG00000170006 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1329083019 Functional Loss SNV dbSNP153 33..33 33 - - - 10898 RMVar_ID_10898 Human_SNP_ID_209032239 A-to-I Human chr4 - 152623687 152623687 152623687 TTAGTAGAGACAGGGTTTCGCCATGTTGGCCAAGCTAGTCTCAAACTCCTGGGCTCAAGTGATCC TTAGTAGAGACAGGGTTTCGCCATGTTGGCCAGGCTAGTCTCAAACTCCTGGGCTCAAGTGATCC T C TMEM154 Ensembl:ENSG00000170006 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1463283585 Functional Loss SNV dbSNP153 33..33 33 - - - 10899 RMVar_ID_10899 Human_SNP_ID_209032262 A-to-I Human chr4 - 152623770 152623770 152623770 TCAGGCGATCCTCCTGCCCCAGCCTCCCAAGTAGCTGGGATTACAGGCGTGCACAACTGCATGCA TCAGGCGATCCTCCTGCCCCAGCCTCCCAAGTGGCTGGGATTACAGGCGTGCACAACTGCATGCA T C TMEM154 Ensembl:ENSG00000170006 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1302032566 Functional Loss SNV dbSNP153 33..33 33 - - - 10900 RMVar_ID_10900 Human_SNP_ID_209032263 A-to-I Human chr4 - 152623773 152623773 152623773 GGCTCAGGCGATCCTCCTGCCCCAGCCTCCCAAGTAGCTGGGATTACAGGCGTGCACAACTGCAT GGCTCAGGCGATCCTCCTGCCCCAGCCTCCCACGTAGCTGGGATTACAGGCGTGCACAACTGCAT T G TMEM154 Ensembl:ENSG00000170006 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1396211256 Functional Loss SNV dbSNP153 33..33 33 - - - 10901 RMVar_ID_10901 Human_SNP_ID_209032264 A-to-I Human chr4 - 152623774 152623774 152623774 AGGCTCAGGCGATCCTCCTGCCCCAGCCTCCCAAGTAGCTGGGATTACAGGCGTGCACAACTGCA AGGCTCAGGCGATCCTCCTGCCCCAGCCTCCCGAGTAGCTGGGATTACAGGCGTGCACAACTGCA T C TMEM154 Ensembl:ENSG00000170006 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1464494580 Functional Loss SNV dbSNP153 33..33 33 - - - 10902 RMVar_ID_10902 Human_SNP_ID_209071738 A-to-I Human chr4 + 152788141 152788141 152788141 TGTAATTCCAGCTACTTGGGAGGTTGAGGTGGAAGATCGTTTGAACCTGGGAGGCAGAGGTTGCA TGTAATTCCAGCTACTTGGGAGGTTGAGGTGGGAGATCGTTTGAACCTGGGAGGCAGAGGTTGCA A G ARFIP1 Ensembl:ENSG00000164144 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1253669570 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111657,RMVar_hsa_circ_229173 10903 RMVar_ID_10903 Human_SNP_ID_209072430 A-to-I Human chr4 + 152790827 152790827 152790827 ACAGTCTCGGCTTACTGCAACCTCTGCCTCCCAGGTTAAGCGATCCTCCTACCTCAGCTTCCTGA ACAGTCTCGGCTTACTGCAACCTCTGCCTCCCCGGTTAAGCGATCCTCCTACCTCAGCTTCCTGA A C ARFIP1 Ensembl:ENSG00000164144 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388900976 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15078108 RMVar_hsa_circ_111657,RMVar_hsa_circ_229173 10904 RMVar_ID_10904 Human_SNP_ID_209072431 A-to-I Human chr4 + 152790827 152790827 152790827 ACAGTCTCGGCTTACTGCAACCTCTGCCTCCCAGGTTAAGCGATCCTCCTACCTCAGCTTCCTGA ACAGTCTCGGCTTACTGCAACCTCTGCCTCCCGGGTTAAGCGATCCTCCTACCTCAGCTTCCTGA A G ARFIP1 Ensembl:ENSG00000164144 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388900976 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15078108 RMVar_hsa_circ_111657,RMVar_hsa_circ_229173 10905 RMVar_ID_10905 Human_SNP_ID_209101691 A-to-I Human chr4 - 152911638 152911638 152911638 ATAACAAATCTTACAGTCCACAAAGTTCATGTATAACGGTAATTTTAAGTACTTCATTTCAACAC ATAACAAATCTTACAGTCCACAAAGTTCATGTGTAACGGTAATTTTAAGTACTTCATTTCAACAC T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs533466861 Functional Loss SNV dbSNP153 33..33 33 - - - 10906 RMVar_ID_10906 Human_SNP_ID_209117904 A-to-I Human chr4 + 152977158 152977158 152977158 TTCATGCCTGTAATCCAGCACTTTGGGAGGCTAAGATGAGTGGATTGCTTGAGCCTAGGAGTTCG TTCATGCCTGTAATCCAGCACTTTGGGAGGCTCAGATGAGTGGATTGCTTGAGCCTAGGAGTTCG A C FHDC1 Ensembl:ENSG00000137460 Protein coding 3'UTR GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs1229661054 Functional Loss SNV dbSNP153 33..33 33 - - - 10907 RMVar_ID_10907 Human_SNP_ID_209117906 A-to-I Human chr4 + 152977164 152977164 152977164 CCTGTAATCCAGCACTTTGGGAGGCTAAGATGAGTGGATTGCTTGAGCCTAGGAGTTCGAGACCA CCTGTAATCCAGCACTTTGGGAGGCTAAGATGCGTGGATTGCTTGAGCCTAGGAGTTCGAGACCA A C FHDC1 Ensembl:ENSG00000137460 Protein coding 3'UTR GSE99789;GSE126723:GSM3611830,GSM3611831,GSM3611832 esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BERP35T1 cell line - 29796672,31158229 RNA-Seq:(High) rs940751632 Functional Loss SNV dbSNP153 33..33 33 - - - 10908 RMVar_ID_10908 Human_SNP_ID_209117907 A-to-I Human chr4 + 152977164 152977164 152977164 CCTGTAATCCAGCACTTTGGGAGGCTAAGATGAGTGGATTGCTTGAGCCTAGGAGTTCGAGACCA CCTGTAATCCAGCACTTTGGGAGGCTAAGATGTGTGGATTGCTTGAGCCTAGGAGTTCGAGACCA A T FHDC1 Ensembl:ENSG00000137460 Protein coding 3'UTR GSE99789;GSE126723:GSM3611830,GSM3611831,GSM3611832 esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BERP35T1 cell line - 29796672,31158229 RNA-Seq:(High) rs940751632 Functional Loss SNV dbSNP153 33..33 33 - - - 10909 RMVar_ID_10909 Human_SNP_ID_209117917 A-to-I Human chr4 + 152977205 152977205 152977205 CTTGAGCCTAGGAGTTCGAGACCAGCCTAGGCAACATGGAGAAACCCCGTCTCTATCAGAAATAC CTTGAGCCTAGGAGTTCGAGACCAGCCTAGGCGACATGGAGAAACCCCGTCTCTATCAGAAATAC A G FHDC1 Ensembl:ENSG00000137460 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1157256154 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26518182 10910 RMVar_ID_10910 Human_SNP_ID_209117918 A-to-I Human chr4 + 152977208 152977208 152977208 GAGCCTAGGAGTTCGAGACCAGCCTAGGCAACATGGAGAAACCCCGTCTCTATCAGAAATACAAA GAGCCTAGGAGTTCGAGACCAGCCTAGGCAACGTGGAGAAACCCCGTCTCTATCAGAAATACAAA A G FHDC1 Ensembl:ENSG00000137460 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1473574114 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26518182 Human_miRNA_ID_266415 10911 RMVar_ID_10911 Human_SNP_ID_209118005 A-to-I Human chr4 + 152977536 152977536 152977536 ACAATCATAGCTCACTGCAGCTTTGACCTCCCAGACCCAAGTGATCCTCCCACCTCAGCCTCCCT ACAATCATAGCTCACTGCAGCTTTGACCTCCCGGACCCAAGTGATCCTCCCACCTCAGCCTCCCT A G FHDC1 Ensembl:ENSG00000137460 Protein coding 3'UTR GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs562438467 Functional Loss SNV dbSNP153 33..33 33 - - - 10912 RMVar_ID_10912 Human_SNP_ID_209182935 A-to-I Human chr4 + 153239327 153239327 153239327 TGAGCCGAGATCGTGCCACTGCACTCCAGCCTAGGAGACACAGCGTGACTCCGTCTCAAAAAAAA TGAGCCGAGATCGTGCCACTGCACTCCAGCCTGGGAGACACAGCGTGACTCCGTCTCAAAAAAAA A G TRIM2 Ensembl:ENSG00000109654 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1445938663 Functional Loss SNV dbSNP153 33..33 33 - - - 10913 RMVar_ID_10913 Human_SNP_ID_209213234 A-to-I Human chr4 + 153364442 153364441 153364443 GAGAGGCTGAGGTGGGAGGATCGCGTGAGCCTAAGAGTTTGAGGTTGCAGTGAGCTGTATTCGTG GAGAGGCTGAGGTGGGAGGATCGCGTGAGCCT__GAGTTTGAGGTTGCAGTGAGCTGTATTCGTG TAA T MND1 Ensembl:ENSG00000121211 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1450054747 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 10914 RMVar_ID_10914 Human_SNP_ID_209213235 A-to-I Human chr4 + 153364442 153364442 153364442 GAGAGGCTGAGGTGGGAGGATCGCGTGAGCCTAAGAGTTTGAGGTTGCAGTGAGCTGTATTCGTG GAGAGGCTGAGGTGGGAGGATCGCGTGAGCCTTAGAGTTTGAGGTTGCAGTGAGCTGTATTCGTG A T MND1 Ensembl:ENSG00000121211 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1268512421 Functional Loss SNV dbSNP153 33..33 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 10915 RMVar_ID_10915 Human_SNP_ID_209213542 A-to-I Human chr4 + 153365669 153365669 153365669 TCACCCAGGCTGGAGTGCAGGGGCACAATCATAGCTCACTGCAGCCTTCAACTCCTGGGCTCAAG TCACCCAGGCTGGAGTGCAGGGGCACAATCATGGCTCACTGCAGCCTTCAACTCCTGGGCTCAAG A G MND1 Ensembl:ENSG00000121211 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459534708 Functional Loss SNV dbSNP153 33..33 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 10916 RMVar_ID_10916 Human_SNP_ID_209214518 A-to-I Human chr4 + 153370121 153370121 153370121 CTAGCCAACATCGTGAAACCCTGTCTCTACTTAAAATACAAAGATCAGCCGGACGTGGTGGCATA CTAGCCAACATCGTGAAACCCTGTCTCTACTTCAAATACAAAGATCAGCCGGACGTGGTGGCATA A C MND1 Ensembl:ENSG00000121211 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs889301585 Functional Loss SNV dbSNP153 33..33 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 10917 RMVar_ID_10917 Human_SNP_ID_209214520 A-to-I Human chr4 + 153370129 153370129 153370129 CATCGTGAAACCCTGTCTCTACTTAAAATACAAAGATCAGCCGGACGTGGTGGCATACGCCTGGA CATCGTGAAACCCTGTCTCTACTTAAAATACAGAGATCAGCCGGACGTGGTGGCATACGCCTGGA A G MND1 Ensembl:ENSG00000121211 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs778405323 Functional Loss SNV dbSNP153 33..33 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 10918 RMVar_ID_10918 Human_SNP_ID_209214633 A-to-I Human chr4 + 153370584 153370584 153370584 CTCTGTCATCCAGGCTGGAGTGCAGTGGCGCGATCCTAGCTCACTGCAACCTCCGCCTCCCGGGT CTCTGTCATCCAGGCTGGAGTGCAGTGGCGCGTTCCTAGCTCACTGCAACCTCCGCCTCCCGGGT A T MND1 Ensembl:ENSG00000121211 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1229400953 Functional Loss SNV dbSNP153 33..33 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 10919 RMVar_ID_10919 Human_SNP_ID_209214646 A-to-I Human chr4 + 153370619 153370619 153370619 CTAGCTCACTGCAACCTCCGCCTCCCGGGTTCAGGTGATTCTCTGGTCTCAGCCTCCTGAGTAGC CTAGCTCACTGCAACCTCCGCCTCCCGGGTTCGGGTGATTCTCTGGTCTCAGCCTCCTGAGTAGC A G MND1 Ensembl:ENSG00000121211 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1362916412 Functional Loss SNV dbSNP153 33..33 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 10920 RMVar_ID_10920 Human_SNP_ID_209214659 A-to-I Human chr4 + 153370700 153370700 153370700 CACCATCACGCCTGGCTAACTTTTGTATTTTTAGTAGAGACAGGGTTTCACGATGTTGGCCAGGC CACCATCACGCCTGGCTAACTTTTGTATTTTTGGTAGAGACAGGGTTTCACGATGTTGGCCAGGC A G MND1 Ensembl:ENSG00000121211 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1271793166 Functional Loss SNV dbSNP153 33..33 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 10921 RMVar_ID_10921 Human_SNP_ID_209219791 A-to-I Human chr4 + 153391606 153391606 153391606 AAAATTCGTCGGATGTGGTGGTGGGTGCCTGTAATCCCAGCTACTCCAGAGGCTGAGGCAGCAGA AAAATTCGTCGGATGTGGTGGTGGGTGCCTGTGATCCCAGCTACTCCAGAGGCTGAGGCAGCAGA A G MND1 Ensembl:ENSG00000121211 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1052762463 Functional Loss SNV dbSNP153 33..33 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 10922 RMVar_ID_10922 Human_SNP_ID_209240943 A-to-I Human chr4 + 153476133 153476133 153476133 GGTGCACACAATCACGCCCGGCTAATTTTTGTATTTTTAGTAGAGATGAGGTTTCACCATGTTGG GGTGCACACAATCACGCCCGGCTAATTTTTGTGTTTTTAGTAGAGATGAGGTTTCACCATGTTGG A G TMEM131L Ensembl:ENSG00000121210 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs534627642 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111567,RMVar_hsa_circ_229225,RMVar_hsa_circ_89179,RMVar_hsa_circ_229224 10923 RMVar_ID_10923 Human_SNP_ID_209242577 A-to-I Human chr4 + 153482731 153482731 153482731 CTTCCGCCTCAGCCTCTCCAGTAGCTGGGGCTACAGGTACACGTCACCATGCCCGGCTAATATTT CTTCCGCCTCAGCCTCTCCAGTAGCTGGGGCTTCAGGTACACGTCACCATGCCCGGCTAATATTT A T TMEM131L Ensembl:ENSG00000121210 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1230346684 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111567,RMVar_hsa_circ_229225,RMVar_hsa_circ_89179,RMVar_hsa_circ_229224 10924 RMVar_ID_10924 Human_SNP_ID_209242797 A-to-I Human chr4 + 153483577 153483577 153483577 AAAAAAAAAGTGGGGCGTGGTGATGTGCACCTATAGGCCCAGCTACTCGGCAGGCTGAGGCTCAC AAAAAAAAAGTGGGGCGTGGTGATGTGCACCTGTAGGCCCAGCTACTCGGCAGGCTGAGGCTCAC A G TMEM131L Ensembl:ENSG00000121210 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs775604652 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111567,RMVar_hsa_circ_229225,RMVar_hsa_circ_89179,RMVar_hsa_circ_229224 10925 RMVar_ID_10925 Human_SNP_ID_209245015 A-to-I Human chr4 + 153491784 153491784 153491784 GCTGGAGTTCGGTAGCCCAGTCTTGGCTCACTACAACCTCAGACTCCCGGGCTCAAGCCATCCTT GCTGGAGTTCGGTAGCCCAGTCTTGGCTCACTGCAACCTCAGACTCCCGGGCTCAAGCCATCCTT A G TMEM131L Ensembl:ENSG00000121210 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs948966795 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111567,RMVar_hsa_circ_229225,RMVar_hsa_circ_89179,RMVar_hsa_circ_229224 10926 RMVar_ID_10926 Human_SNP_ID_209245895 A-to-I Human chr4 + 153495105 153495105 153495105 TGGGAGGCCGAGGCGGTGGATCATCTGAGGTCAGTAGTTTGAGATCAGCCTTGCCAACATGCTGA TGGGAGGCCGAGGCGGTGGATCATCTGAGGTCTGTAGTTTGAGATCAGCCTTGCCAACATGCTGA A T TMEM131L Ensembl:ENSG00000121210 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs936761789 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15080304 RMVar_hsa_circ_111567,RMVar_hsa_circ_229225,RMVar_hsa_circ_89179,RMVar_hsa_circ_229224 10927 RMVar_ID_10927 Human_SNP_ID_209245909 A-to-I Human chr4 + 153495168 153495168 153495168 GAAACCCCATCTCTACTAAAAATACAAAAATTAGCCGGGCGTGGTGGTATGCACCAGTAGTCCCA GAAACCCCATCTCTACTAAAAATACAAAAATTGGCCGGGCGTGGTGGTATGCACCAGTAGTCCCA A G TMEM131L Ensembl:ENSG00000121210 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs886369678 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111567,RMVar_hsa_circ_229225,RMVar_hsa_circ_89179,RMVar_hsa_circ_229224 10928 RMVar_ID_10928 Human_SNP_ID_209259892 A-to-I Human chr4 + 153551539 153551539 153551539 GCCACCACGCCTGTAATTTTTGTATTTTTAGTAGAGACAGTGTTTTGCCATGTTGGCCAGGCTAG GCCACCACGCCTGTAATTTTTGTATTTTTAGTGGAGACAGTGTTTTGCCATGTTGGCCAGGCTAG A G TMEM131L Ensembl:ENSG00000121210 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1257692225 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111567,RMVar_hsa_circ_229225,RMVar_hsa_circ_89179,RMVar_hsa_circ_287502,RMVar_hsa_circ_229224,RMVar_hsa_circ_347428,RMVar_hsa_circ_229226 10929 RMVar_ID_10929 Human_SNP_ID_209262871 A-to-I Human chr4 + 153563668 153563668 153563668 TTTTGTATTTTTTGTAGAGACAAGATTTTGCCATGTTGCCCTGCCTGGTCTCAAACTCTTGGACT TTTTGTATTTTTTGTAGAGACAAGATTTTGCCGTGTTGCCCTGCCTGGTCTCAAACTCTTGGACT A G TMEM131L Ensembl:ENSG00000121210 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs951272166 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111567,RMVar_hsa_circ_229225,RMVar_hsa_circ_56652,RMVar_hsa_circ_377488 10930 RMVar_ID_10930 Human_SNP_ID_209266508 A-to-I Human chr4 + 153578222 153578222 153578222 TTAGTTAAAGCAGTTTCAGAGCTGGGCATGGTAGTGCACGCTTGTAGTCCCAGCTACTCAGGAGG TTAGTTAAAGCAGTTTCAGAGCTGGGCATGGTGGTGCACGCTTGTAGTCCCAGCTACTCAGGAGG A G TMEM131L Ensembl:ENSG00000121210 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1047139804 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15080814 RMVar_hsa_circ_111567,RMVar_hsa_circ_229225,RMVar_hsa_circ_56652,RMVar_hsa_circ_377488 10931 RMVar_ID_10931 Human_SNP_ID_209278308 A-to-I Human chr4 + 153624248 153624248 153624248 TTAAGCGATTCTTGTGCCTCAGCCTCCCAAGTAGCTGGGGTTACAGGCATGTGCCACCATGCCCG TTAAGCGATTCTTGTGCCTCAGCCTCCCAAGTGGCTGGGGTTACAGGCATGTGCCACCATGCCCG A G TMEM131L Ensembl:ENSG00000121210 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs189524370 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25788352 RMVar_hsa_circ_118815,RMVar_hsa_circ_229232,RMVar_hsa_circ_10840,RMVar_hsa_circ_92493,RMVar_hsa_circ_76205,RMVar_hsa_circ_229235,RMVar_hsa_circ_124106,RMVar_hsa_circ_229237,RMVar_hsa_circ_229238,RMVar_hsa_circ_366728,RMVar_hsa_circ_124827,RMVar_hsa_circ_56097,RMVar_hsa_circ_229247,RMVar_hsa_circ_66352,RMVar_hsa_circ_88168,RMVar_hsa_circ_229248 10932 RMVar_ID_10932 Human_SNP_ID_209278318 A-to-I Human chr4 + 153624284 153624284 153624284 GGGGTTACAGGCATGTGCCACCATGCCCGTCTAATTTTTGTATTGTTAGTAGAGACGGGGTTTCA GGGGTTACAGGCATGTGCCACCATGCCCGTCTCATTTTTGTATTGTTAGTAGAGACGGGGTTTCA A C TMEM131L Ensembl:ENSG00000121210 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs555678773 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118815,RMVar_hsa_circ_229232,RMVar_hsa_circ_10840,RMVar_hsa_circ_92493,RMVar_hsa_circ_76205,RMVar_hsa_circ_229235,RMVar_hsa_circ_124106,RMVar_hsa_circ_229237,RMVar_hsa_circ_229238,RMVar_hsa_circ_366728,RMVar_hsa_circ_124827,RMVar_hsa_circ_56097,RMVar_hsa_circ_229247,RMVar_hsa_circ_66352,RMVar_hsa_circ_88168,RMVar_hsa_circ_229248 10933 RMVar_ID_10933 Human_SNP_ID_209278319 A-to-I Human chr4 + 153624284 153624284 153624284 GGGGTTACAGGCATGTGCCACCATGCCCGTCTAATTTTTGTATTGTTAGTAGAGACGGGGTTTCA GGGGTTACAGGCATGTGCCACCATGCCCGTCTGATTTTTGTATTGTTAGTAGAGACGGGGTTTCA A G TMEM131L Ensembl:ENSG00000121210 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs555678773 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118815,RMVar_hsa_circ_229232,RMVar_hsa_circ_10840,RMVar_hsa_circ_92493,RMVar_hsa_circ_76205,RMVar_hsa_circ_229235,RMVar_hsa_circ_124106,RMVar_hsa_circ_229237,RMVar_hsa_circ_229238,RMVar_hsa_circ_366728,RMVar_hsa_circ_124827,RMVar_hsa_circ_56097,RMVar_hsa_circ_229247,RMVar_hsa_circ_66352,RMVar_hsa_circ_88168,RMVar_hsa_circ_229248 10934 RMVar_ID_10934 Human_SNP_ID_209504803 A-to-I Human chr4 + 154555954 154555954 154555954 CAAACATGTCAGCCCAGCAGATGCTGCTGTTGAAATTCCACTCAGTGAAAATGAGGCCAAAGTCT CAAACATGTCAGCCCAGCAGATGCTGCTGTTGTAATTCCACTCAGTGAAAATGAGGCCAAAGTCT A T AC107385.1 Ensembl:ENSG00000248611 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1476328492 Functional Loss SNV dbSNP153 33..33 33 - - - 10935 RMVar_ID_10935 Human_SNP_ID_210088476 A-to-I Human chr4 - 156901884 156901884 156901884 TACCTGGCCAGGCTCCGTGGCTCATGCCTATAATTCCAGAACTTTGGGAGGCCGAGGCGGGCAGA TACCTGGCCAGGCTCCGTGGCTCATGCCTATAGTTCCAGAACTTTGGGAGGCCGAGGCGGGCAGA T C PDGFC Ensembl:ENSG00000145431 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs949669164 Functional Loss SNV dbSNP153 33..33 33 - - - 10936 RMVar_ID_10936 Human_SNP_ID_210176235 A-to-I Human chr4 + 157248912 157248912 157248912 CAGACTGGAGTGCAGTGGGATGATCTTGGCTCACTGTAACTTTAACCTCCTGGAATCAAGCAATC CAGACTGGAGTGCAGTGGGATGATCTTGGCTCGCTGTAACTTTAACCTCCTGGAATCAAGCAATC A G GRIA2 Ensembl:ENSG00000120251 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs951609226 Functional Loss SNV dbSNP153 33..33 33 - - - 10937 RMVar_ID_10937 Human_SNP_ID_210176237 A-to-I Human chr4 + 157248917 157248917 157248917 TGGAGTGCAGTGGGATGATCTTGGCTCACTGTAACTTTAACCTCCTGGAATCAAGCAATCCTCTC TGGAGTGCAGTGGGATGATCTTGGCTCACTGTGACTTTAACCTCCTGGAATCAAGCAATCCTCTC A G GRIA2 Ensembl:ENSG00000120251 Protein coding intron GSE107867 ASD brains,frontal_cortex;ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs908634309 Functional Loss SNV dbSNP153 33..33 33 - - - 10938 RMVar_ID_10938 Human_SNP_ID_210197426 A-to-I Human chr4 + 157336723 157336723 157336723 TAGTCTCTGGTTTTCCTTGGGTGCCTTTATGCAGCAAGGATGCGATATTTCGCCAAGGTTGGTTA TAGTCTCTGGTTTTCCTTGGGTGCCTTTATGCGGCAAGGATGCGATATTTCGCCAAGGTTGGTTA A G GRIA2 Ensembl:ENSG00000120251 Protein coding CDS GSE56152 embryonic stem cells,wild type - 25708366 RNA-Seq:(High) rs17850674 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9151903 Human_Splice_Rec_618491,Human_Splice_Rec_618521,Human_Splice_Rec_618557,Human_Splice_Rec_618585,Human_Splice_Rec_618615,Human_Splice_Rec_618645,Human_Splice_Rec_618679 RMVar_hsa_circ_96,RMVar_hsa_circ_9118,RMVar_hsa_circ_378117,RMVar_hsa_circ_49848,RMVar_hsa_circ_37239,RMVar_hsa_circ_21630,RMVar_hsa_circ_37475,RMVar_hsa_circ_19299,RMVar_hsa_circ_24108,RMVar_hsa_circ_229297,RMVar_hsa_circ_229298,RMVar_hsa_circ_229299,RMVar_hsa_circ_330427 10939 RMVar_ID_10939 Human_SNP_ID_210197427 A-to-I Human chr4 + 157336726 157336726 157336726 TCTCTGGTTTTCCTTGGGTGCCTTTATGCAGCAAGGATGCGATATTTCGCCAAGGTTGGTTACTC TCTCTGGTTTTCCTTGGGTGCCTTTATGCAGCGAGGATGCGATATTTCGCCAAGGTTGGTTACTC A G GRIA2 Ensembl:ENSG00000120251 Protein coding CDS GSE56152;GSE107867;GSE123020:GSM3490832,GSM3490833,GSM3490834 embryonic stem cells,wild type;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;esophageal squamous carcinoma cells,KYSE180 cell line - 25708366,30559470,32596459 RNA-Seq:(High) rs17850675 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9151903 Human_Splice_Rec_618491,Human_Splice_Rec_618521,Human_Splice_Rec_618557,Human_Splice_Rec_618585,Human_Splice_Rec_618615,Human_Splice_Rec_618645,Human_Splice_Rec_618679 RMVar_hsa_circ_96,RMVar_hsa_circ_9118,RMVar_hsa_circ_378117,RMVar_hsa_circ_49848,RMVar_hsa_circ_37239,RMVar_hsa_circ_21630,RMVar_hsa_circ_37475,RMVar_hsa_circ_19299,RMVar_hsa_circ_24108,RMVar_hsa_circ_229297,RMVar_hsa_circ_229298,RMVar_hsa_circ_229299,RMVar_hsa_circ_330427 10940 RMVar_ID_10940 Human_SNP_ID_210200129 A-to-I Human chr4 + 157348448 157348448 157348448 TTTTGTAGAAACGAGATCTCCCTATGTTGCCCAGGCTGGTCTCGAGCTCCTGGGCTCAAGTGATC TTTTGTAGAAACGAGATCTCCCTATGTTGCCCGGGCTGGTCTCGAGCTCCTGGGCTCAAGTGATC A G GRIA2 Ensembl:ENSG00000120251 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1337068935 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_378117,RMVar_hsa_circ_37475,RMVar_hsa_circ_24554,RMVar_hsa_circ_19299,RMVar_hsa_circ_24108,RMVar_hsa_circ_229297,RMVar_hsa_circ_229298,RMVar_hsa_circ_229299,RMVar_hsa_circ_330427 10941 RMVar_ID_10941 Human_SNP_ID_210525002 A-to-I Human chr4 + 158678748 158678748 158678748 TAGCTCACTGTAGCCTCGAATTACTGGGCTCTAGTGATCATCGTACCTCAGCCTCCTGAGTAGGT TAGCTCACTGTAGCCTCGAATTACTGGGCTCTGGTGATCATCGTACCTCAGCCTCCTGAGTAGGT A G ETFDH Ensembl:ENSG00000171503 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs966370128 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15083490 10942 RMVar_ID_10942 Human_SNP_ID_210525028 A-to-I Human chr4 + 158678848 158678848 158678848 TTTTTTACTTTTTATTTTTTATTTCTGTAGAGAAGAGGTCTTGCTATATTGCCTAGGAGGATCTT TTTTTTACTTTTTATTTTTTATTTCTGTAGAGGAGAGGTCTTGCTATATTGCCTAGGAGGATCTT A G ETFDH Ensembl:ENSG00000171503 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs960732876 Functional Loss SNV dbSNP153 33..33 33 - - - 10943 RMVar_ID_10943 Human_SNP_ID_210525228 A-to-I Human chr4 + 158679888 158679888 158679888 GAGGCCAGGAGTTCGAGACCAGCCTGGCCAACATGGCAAAACCGCATCTCTACTAAAAAAAAAAA GAGGCCAGGAGTTCGAGACCAGCCTGGCCAACGTGGCAAAACCGCATCTCTACTAAAAAAAAAAA A G ETFDH Ensembl:ENSG00000171503 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1394248144 Functional Loss SNV dbSNP153 33..33 33 - - - 10944 RMVar_ID_10944 Human_SNP_ID_210525251 A-to-I Human chr4 + 158679938 158679938 158679938 TACTAAAAAAAAAAAACAAAAATCCAAAAATTAGCTGGGTGTGGTGGTGCACACCTGTAGTCCCA TACTAAAAAAAAAAAACAAAAATCCAAAAATTTGCTGGGTGTGGTGGTGCACACCTGTAGTCCCA A T ETFDH Ensembl:ENSG00000171503 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1374668753 Functional Loss SNV dbSNP153 33..33 33 - - - 10945 RMVar_ID_10945 Human_SNP_ID_210528178 A-to-I Human chr4 + 158691525 158691525 158691525 TTTTGTATTTTTATTAGAGATGGGGTTTTGCCATGTTGGCCACGCTGGTCTTGAACTCCTGTCCT TTTTGTATTTTTATTAGAGATGGGGTTTTGCCGTGTTGGCCACGCTGGTCTTGAACTCCTGTCCT A G ETFDH Ensembl:ENSG00000171503 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs889928198 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55738,RMVar_hsa_circ_355959,RMVar_hsa_circ_367909,RMVar_hsa_circ_315099,RMVar_hsa_circ_60062 10946 RMVar_ID_10946 Human_SNP_ID_210549732 A-to-I Human chr4 + 158780165 158780165 158780165 AAGAGGTTGAGGCTTTAGTGAGCCATGATCGCACCACTGTACTCTAGCCTGGGTGACAGAGGGAG AAGAGGTTGAGGCTTTAGTGAGCCATGATCGCCCCACTGTACTCTAGCCTGGGTGACAGAGGGAG A C FNIP2 Ensembl:ENSG00000052795 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs544214586 Functional Loss SNV dbSNP153 33..33 33 - - - 10947 RMVar_ID_10947 Human_SNP_ID_210562346 A-to-I Human chr4 + 158836693 158836693 158836693 AAGAAATTAGCCAGGCGTGGTGGCGCATACCTATAGTCCTAGCTACTCAGGAGGCTGAGGCACGA AAGAAATTAGCCAGGCGTGGTGGCGCATACCTGTAGTCCTAGCTACTCAGGAGGCTGAGGCACGA A G FNIP2 Ensembl:ENSG00000052795 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs534250036 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38820,RMVar_hsa_circ_352139,RMVar_hsa_circ_366746,RMVar_hsa_circ_82194,RMVar_hsa_circ_229334,RMVar_hsa_circ_229335,RMVar_hsa_circ_125219,RMVar_hsa_circ_49702,RMVar_hsa_circ_94468,RMVar_hsa_circ_229336,RMVar_hsa_circ_229337 10948 RMVar_ID_10948 Human_SNP_ID_210630572 A-to-I Human chr4 + 159123631 159123625 159123632 CTCGATCTCAGCTGGGTTCACGCCATTCTCCTACCTCAGCCTCCCGAGTAGCTGGGACTACAGGC CTCGATCTCAGCTGGGTTCACGCCATT_______CTCAGCCTCCCGAGTAGCTGGGACTACAGGC TCTCCTAC T RAPGEF2 Ensembl:ENSG00000109756 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1393028104 Functional Loss DEL dbSNP153 28..34 33 - - - 10949 RMVar_ID_10949 Human_SNP_ID_210663743 A-to-I Human chr4 + 159254801 159254801 159254801 TGGCTAATTTTTAGTAGAAACAGGGTTTGACCATATTGGCCAGGCTGGTCTCGAACTCTTAACCT TGGCTAATTTTTAGTAGAAACAGGGTTTGACCGTATTGGCCAGGCTGGTCTCGAACTCTTAACCT A G RAPGEF2 Ensembl:ENSG00000109756 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1231760914 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 10950 RMVar_ID_10950 Human_SNP_ID_211248259 A-to-I Human chr4 - 161519270 161519270 161519270 CATTCACCCCGGTCTCCCAAAGTGCTGGGATTACAAGCATGAGCCACCATGCCACTCTAAGACTG CATTCACCCCGGTCTCCCAAAGTGCTGGGATTGCAAGCATGAGCCACCATGCCACTCTAAGACTG T C FSTL5 Ensembl:ENSG00000168843 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1269410604 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6048,RMVar_hsa_circ_671,RMVar_hsa_circ_328035,RMVar_hsa_circ_229383,RMVar_hsa_circ_41512,RMVar_hsa_circ_312224,RMVar_hsa_circ_268545 10951 RMVar_ID_10951 Human_SNP_ID_211281073 A-to-I Human chr4 - 161644487 161644487 161644487 AGTTTCATTCTTATTGCCCTGGCTGCAGTGCAATGGTGCGGCCTCGGCTCACTACAACCTCCACC AGTTTCATTCTTATTGCCCTGGCTGCAGTGCAGTGGTGCGGCCTCGGCTCACTACAACCTCCACC T C FSTL5 Ensembl:ENSG00000168843 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1418869115 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6048,RMVar_hsa_circ_671,RMVar_hsa_circ_268545,RMVar_hsa_circ_313774,RMVar_hsa_circ_24911,RMVar_hsa_circ_25569 10952 RMVar_ID_10952 Human_SNP_ID_211299280 A-to-I Human chr4 - 161716475 161716475 161716475 CTCCTGCCTCAGCCTCCCTAGTAGCTGAGACTACAGGCACACACCACCAAACTCGGCTCACTTTG CTCCTGCCTCAGCCTCCCTAGTAGCTGAGACTCCAGGCACACACCACCAAACTCGGCTCACTTTG T G FSTL5 Ensembl:ENSG00000168843 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1389371792 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268545,RMVar_hsa_circ_313774,RMVar_hsa_circ_24911,RMVar_hsa_circ_25569 10953 RMVar_ID_10953 Human_SNP_ID_211344497 A-to-I Human chr4 - 161894558 161894558 161894558 AGAATCGCTTGAACCTGGGAGGTGGAAGTTGCAGTGAGCCAAGATTGAGCCACTGTATTCCAGCC AGAATCGCTTGAACCTGGGAGGTGGAAGTTGCGGTGAGCCAAGATTGAGCCACTGTATTCCAGCC T C FSTL5 Ensembl:ENSG00000168843 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1356279492 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19608,RMVar_hsa_circ_268545,RMVar_hsa_circ_24911,RMVar_hsa_circ_32632 10954 RMVar_ID_10954 Human_SNP_ID_211372654 A-to-I Human chr4 - 162007190 162007190 162007190 AAATTTGGGCTTGCTTAACATAGCACTCCTCTAGGATAGCAATTCGCTTTATGTCATTTTAAATT AAATTTGGGCTTGCTTAACATAGCACTCCTCTGGGATAGCAATTCGCTTTATGTCATTTTAAATT T C FSTL5 Ensembl:ENSG00000168843 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1311544772 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24911,RMVar_hsa_circ_32632 10955 RMVar_ID_10955 Human_SNP_ID_211372984 A-to-I Human chr4 - 162008745 162008744 162008745 TAGTAAATATTTAAAAAGAATGGCCTAAAGTCATTTATGCTAAAGGAGATCAGAGCCCAGCAGTT TAGTAAATATTTAAAAAGAATGGCCTAAAGTC_TTTATGCTAAAGGAGATCAGAGCCCAGCAGTT AT A FSTL5 Ensembl:ENSG00000168843 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1234167916 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_24911,RMVar_hsa_circ_32632 10956 RMVar_ID_10956 Human_SNP_ID_211387976 A-to-I Human chr4 - 162070103 162070103 162070103 ATGTAACTTATCATCAGGAAAATGCAAACCAAAACCACATGAGATATTACCTCACCCAAGACAGA ATGTAACTTATCATCAGGAAAATGCAAACCAACACCACATGAGATATTACCTCACCCAAGACAGA T G FSTL5 Ensembl:ENSG00000168843 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1303935300 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24911,RMVar_hsa_circ_32632 10957 RMVar_ID_10957 Human_SNP_ID_211851669 A-to-I Human chr4 + 163932922 163932922 163932922 ACTTCCAGTACTTTGCTGAAGCTGCATGTGGTAATGATCAAAAACAAATGATAGATAATTCCCAA ACTTCCAGTACTTTGCTGAAGCTGCATGTGGTGATGATCAAAAACAAATGATAGATAATTCCCAA A G AC112247.1 Ensembl:ENSG00000177803 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1205379287 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1896292,Human_miRNA_ID_1902264 10958 RMVar_ID_10958 Human_SNP_ID_211851671 A-to-I Human chr4 + 163932929 163932929 163932929 GTACTTTGCTGAAGCTGCATGTGGTAATGATCAAAAACAAATGATAGATAATTCCCAAGGAGCTT GTACTTTGCTGAAGCTGCATGTGGTAATGATCGAAAACAAATGATAGATAATTCCCAAGGAGCTT A G AC112247.1 Ensembl:ENSG00000177803 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1283268211 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7343170,Human_RBP_ID_27725333 Human_miRNA_ID_1896292,Human_miRNA_ID_1902264 10959 RMVar_ID_10959 Human_SNP_ID_211919217 A-to-I Human chr4 + 164189347 164189347 164189347 TGAAGGAGAAGACTTTTCTGAGACCCTGACTCAGGCCAAATTTTAAGAGCTAAACATGGATCTGT TGAAGGAGAAGACTTTTCTGAGACCCTGACTCGGGCCAAATTTTAAGAGCTAAACATGGATCTGT A G AC105250.1 Ensembl:ENSG00000250746 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1434213280 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9165427 10960 RMVar_ID_10960 Human_SNP_ID_212112699 A-to-I Human chr4 - 164943466 164943466 164943466 ATCTGTTTTGCTTTACTGACTGGCTCTTCATCAATTTCAGCTGCTGCCACCAGCTGGGCTTCTTG ATCTGTTTTGCTTTACTGACTGGCTCTTCATCGATTTCAGCTGCTGCCACCAGCTGGGCTTCTTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878926393 Functional Loss SNV dbSNP153 33..33 33 - - - 10961 RMVar_ID_10961 Human_SNP_ID_568551290 A-to-I Human chr14 - 105002790 105002790 105002790 GGTGGCCTGTAGTCACAGCTACTCGGGAGGCTAAGGCAGGAGAATCGCTTGAACCTGGAAGGCGG GGTGGCCTGTAGTCACAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCTGGAAGGCGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1198626267 Functional Loss SNV dbSNP153 33..33 33 - - - 10962 RMVar_ID_10962 Human_SNP_ID_568554716 A-to-I Human chr14 - 105013869 105013869 105013869 ACTACAAATAAAGCTGCTGTGCACATTCTGGAACATGTTTTTTGCATGAACATTGGCTTTTTCTC ACTACAAATAAAGCTGCTGTGCACATTCTGGATCATGTTTTTTGCATGAACATTGGCTTTTTCTC T A CDCA4 Ensembl:ENSG00000170779 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1218201868 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2407663,Human_RBP_ID_3443183,Human_RBP_ID_17562302 10963 RMVar_ID_10963 Human_SNP_ID_568563848 A-to-I Human chr14 - 105049513 105049513 105049513 CACGCCTGTCATCCCAGCACTTTGGGAGGCCGAGACGGGAGGATCAGTTGAGGTCAGGAGTTTGA CACGCCTGTCATCCCAGCACTTTGGGAGGCCGGGACGGGAGGATCAGTTGAGGTCAGGAGTTTGA T C GPR132 Ensembl:ENSG00000183484 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1320367589 Functional Loss SNV dbSNP153 33..33 33 - - - 10964 RMVar_ID_10964 Human_SNP_ID_568563849 A-to-I Human chr14 - 105049513 105049513 105049513 CACGCCTGTCATCCCAGCACTTTGGGAGGCCGAGACGGGAGGATCAGTTGAGGTCAGGAGTTTGA CACGCCTGTCATCCCAGCACTTTGGGAGGCCGCGACGGGAGGATCAGTTGAGGTCAGGAGTTTGA T G GPR132 Ensembl:ENSG00000183484 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1320367589 Functional Loss SNV dbSNP153 33..33 33 - - - 10965 RMVar_ID_10965 Human_SNP_ID_568565425 A-to-I Human chr14 - 105054852 105054852 105054852 TATTTTTAGTAGAGACGAGTTTTCACCAGGTTAGCCAGGCTGGTCTCGAACGCCTGACCTCTAGT TATTTTTAGTAGAGACGAGTTTTCACCAGGTTGGCCAGGCTGGTCTCGAACGCCTGACCTCTAGT T C GPR132 Ensembl:ENSG00000183484 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1366951860 Functional Loss SNV dbSNP153 33..33 33 - - - 10966 RMVar_ID_10966 Human_SNP_ID_568616361 A-to-I Human chr14 - 105223085 105223085 105223085 GGGCTCAAGCAACCCTCCCATCTCAGCCTCCCAAGTAGCTGGGACTGCAGGCGGGCACCACCACA GGGCTCAAGCAACCCTCCCATCTCAGCCTCCCTAGTAGCTGGGACTGCAGGCGGGCACCACCACA T A BRF1 Ensembl:ENSG00000185024 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1013363857 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25086133 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 10967 RMVar_ID_10967 Human_SNP_ID_568616365 A-to-I Human chr14 - 105223098 105223098 105223098 GTGTCAACCTCCTGGGCTCAAGCAACCCTCCCATCTCAGCCTCCCAAGTAGCTGGGACTGCAGGC GTGTCAACCTCCTGGGCTCAAGCAACCCTCCCGTCTCAGCCTCCCAAGTAGCTGGGACTGCAGGC T C BRF1 Ensembl:ENSG00000185024 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs1442946618 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25124908 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 10968 RMVar_ID_10968 Human_SNP_ID_568616375 A-to-I Human chr14 - 105223141 105223141 105223141 TCACCCAGAGTGGAGTGCAATAGTTCCATCATAGCTCACTGCAGTGTCAACCTCCTGGGCTCAAG TCACCCAGAGTGGAGTGCAATAGTTCCATCATCGCTCACTGCAGTGTCAACCTCCTGGGCTCAAG T G BRF1 Ensembl:ENSG00000185024 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs978505490 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_353280,RMVar_hsa_circ_356891,RMVar_hsa_circ_265061 10969 RMVar_ID_10969 Human_SNP_ID_568616743 A-to-I Human chr14 - 105224221 105224221 105224221 GGGACTACAGGCATGCGCCACCACGCCCAGCTAATTTTTGTATTTTTTGTAGAAACGGGGTTTCG GGGACTACAGGCATGCGCCACCACGCCCAGCTGATTTTTGTATTTTTTGTAGAAACGGGGTTTCG T C BRF1 Ensembl:ENSG00000185024 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1302586385 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_353280,RMVar_hsa_circ_356891,RMVar_hsa_circ_265061 10970 RMVar_ID_10970 Human_SNP_ID_568616753 A-to-I Human chr14 - 105224245 105224245 105224245 CCTGCCTCACCCTCCTGAGTAGTTGGGACTACAGGCATGCGCCACCACGCCCAGCTAATTTTTGT CCTGCCTCACCCTCCTGAGTAGTTGGGACTACGGGCATGCGCCACCACGCCCAGCTAATTTTTGT T C BRF1 Ensembl:ENSG00000185024 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs587742768 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_353280,RMVar_hsa_circ_356891,RMVar_hsa_circ_265061 10971 RMVar_ID_10971 Human_SNP_ID_568616853 A-to-I Human chr14 - 105224617 105224617 105224617 CTTGAACCCAGGAGTTCGATGTGCAGTGAGCTATGATTGCACCACTGTATTCCAGCCTGGGCAGC CTTGAACCCAGGAGTTCGATGTGCAGTGAGCTGTGATTGCACCACTGTATTCCAGCCTGGGCAGC T C BRF1 Ensembl:ENSG00000185024 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1325818462 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25086139 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 10972 RMVar_ID_10972 Human_SNP_ID_568617260 A-to-I Human chr14 - 105225892 105225892 105225892 CCTGTAATCCCAGCACTTTAGGAGGCTGAGGCAGGCGGATCACGAGGTCAGGAGATGGAGACCAT CCTGTAATCCCAGCACTTTAGGAGGCTGAGGCGGGCGGATCACGAGGTCAGGAGATGGAGACCAT T C BRF1 Ensembl:ENSG00000185024 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1310283090 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_353280,RMVar_hsa_circ_356891,RMVar_hsa_circ_265061 10973 RMVar_ID_10973 Human_SNP_ID_568626813 A-to-I Human chr14 - 105259272 105259272 105259272 CCCGGCTAATTTTTGGATTTTTTTGTAGAAACAGGGTCTCACTGTGTTGCCCAGGCCGGTCTTGA CCCGGCTAATTTTTGGATTTTTTTGTAGAAACCGGGTCTCACTGTGTTGCCCAGGCCGGTCTTGA T G BRF1 Ensembl:ENSG00000185024 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1014844411 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12287588,Human_RBP_ID_18646781 RMVar_hsa_circ_125310,RMVar_hsa_circ_169697,RMVar_hsa_circ_108620,RMVar_hsa_circ_169696,RMVar_hsa_circ_33213,RMVar_hsa_circ_50010,RMVar_hsa_circ_305011,RMVar_hsa_circ_97507,RMVar_hsa_circ_169704,RMVar_hsa_circ_265922,RMVar_hsa_circ_128008,RMVar_hsa_circ_169709,RMVar_hsa_circ_302563,RMVar_hsa_circ_272285,RMVar_hsa_circ_169708,RMVar_hsa_circ_169711,RMVar_hsa_circ_96431,RMVar_hsa_circ_169710 10974 RMVar_ID_10974 Human_SNP_ID_568628081 A-to-I Human chr14 - 105264220 105264220 105264220 GCTATTCTCCTGCCTTGGCCTCCCAACGTGCTAGGATTATAGATGTGAGCCATCACTAAGACTCC GCTATTCTCCTGCCTTGGCCTCCCAACGTGCTGGGATTATAGATGTGAGCCATCACTAAGACTCC T C BRF1 Ensembl:ENSG00000185024 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1307182073 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_33213,RMVar_hsa_circ_50010,RMVar_hsa_circ_305011,RMVar_hsa_circ_97507,RMVar_hsa_circ_169704,RMVar_hsa_circ_265922,RMVar_hsa_circ_128008,RMVar_hsa_circ_169709,RMVar_hsa_circ_302563,RMVar_hsa_circ_272285,RMVar_hsa_circ_169708,RMVar_hsa_circ_169711,RMVar_hsa_circ_96431,RMVar_hsa_circ_169710 10975 RMVar_ID_10975 Human_SNP_ID_568653316 A-to-I Human chr14 + 105353739 105353739 105353739 CTTCAGCCTCCCGAGCAGCTGGGATTACAGGCATGTGCCACCACGCCCGGCTATTTTTCGTATCT CTTCAGCCTCCCGAGCAGCTGGGATTACAGGCGTGTGCCACCACGCCCGGCTATTTTTCGTATCT A G PACS2 Ensembl:ENSG00000179364 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs138448486 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90970,RMVar_hsa_circ_41918,RMVar_hsa_circ_377088,RMVar_hsa_circ_377947,RMVar_hsa_circ_279581,RMVar_hsa_circ_285492,RMVar_hsa_circ_124251,RMVar_hsa_circ_169714,RMVar_hsa_circ_169715,RMVar_hsa_circ_292932,RMVar_hsa_circ_169716,RMVar_hsa_circ_169717 10976 RMVar_ID_10976 Human_SNP_ID_568654888 A-to-I Human chr14 + 105359377 105359377 105359377 GTTTCACTTTTATAGTGCAGTGGCGCGATCTCAGTTCACTGCAACCTCCACCTCCCGGGTTCAAG GTTTCACTTTTATAGTGCAGTGGCGCGATCTCGGTTCACTGCAACCTCCACCTCCCGGGTTCAAG A G PACS2 Ensembl:ENSG00000179364 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs587690763 Functional Loss SNV dbSNP153 33..33 33 - - - 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_169717 10977 RMVar_ID_10977 Human_SNP_ID_568672303 A-to-I Human chr14 - 105415711 105415711 105415711 TTCAGTATGGATGGAGCTTCCCTTTGTTGCCCAGGCTGTTCTCCAACTCCTGAGCTCAAGCGATC TTCAGTATGGATGGAGCTTCCCTTTGTTGCCCGGGCTGTTCTCCAACTCCTGAGCTCAAGCGATC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1258168145 Functional Loss SNV dbSNP153 33..33 33 - - - 10978 RMVar_ID_10978 Human_SNP_ID_568675934 A-to-I Human chr14 + 105428781 105428781 105428781 TTGCTCTGTTGCCCAGGCTGGAGTGCAGTGGTATGATCTTGGCTCACTGTATGTAGCCTCAGTCT TTGCTCTGTTGCCCAGGCTGGAGTGCAGTGGTGTGATCTTGGCTCACTGTATGTAGCCTCAGTCT A G MTA1,TEX22 Ensembl:ENSG00000182979,Ensembl:ENSG00000226174 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs587765422 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12288498 10979 RMVar_ID_10979 Human_SNP_ID_568683348 A-to-I Human chr14 + 105455089 105455089 105455089 CCACACCCCCCTAGTTTTTTTGTATTTTTATTAGAGACAGGGTTTCGCCATGTTGCCCAGGTTGG CCACACCCCCCTAGTTTTTTTGTATTTTTATTGGAGACAGGGTTTCGCCATGTTGCCCAGGTTGG A G MTA1 Ensembl:ENSG00000182979 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1350006677 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2407843,Human_RBP_ID_12289025 RMVar_hsa_circ_14003,RMVar_hsa_circ_39157,RMVar_hsa_circ_10523,RMVar_hsa_circ_63926,RMVar_hsa_circ_169736,RMVar_hsa_circ_124730,RMVar_hsa_circ_304587,RMVar_hsa_circ_169738,RMVar_hsa_circ_32655 10980 RMVar_ID_10980 Human_SNP_ID_568683350 A-to-I Human chr14 + 105455095 105455094 105455096 CCCCCTAGTTTTTTTGTATTTTTATTAGAGACAGGGTTTCGCCATGTTGCCCAGGTTGGTCTCAA CCCCCTAGTTTTTTTGTATTTTTATTAGAGAC__GGTTTCGCCATGTTGCCCAGGTTGGTCTCAA CAG C MTA1 Ensembl:ENSG00000182979 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1444673757 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_14003,RMVar_hsa_circ_39157,RMVar_hsa_circ_10523,RMVar_hsa_circ_63926,RMVar_hsa_circ_169736,RMVar_hsa_circ_124730,RMVar_hsa_circ_304587,RMVar_hsa_circ_169738,RMVar_hsa_circ_32655 10981 RMVar_ID_10981 Human_SNP_ID_568683361 A-to-I Human chr14 + 105455140 105455140 105455140 GTTGCCCAGGTTGGTCTCAAACCCCTGAACTCAAGTGATCTACCTGCTTCGACCTCCCAAACTGC GTTGCCCAGGTTGGTCTCAAACCCCTGAACTCCAGTGATCTACCTGCTTCGACCTCCCAAACTGC A C MTA1 Ensembl:ENSG00000182979 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1555429584 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12289027,Human_RBP_ID_18646951 RMVar_hsa_circ_14003,RMVar_hsa_circ_39157,RMVar_hsa_circ_10523,RMVar_hsa_circ_63926,RMVar_hsa_circ_169736,RMVar_hsa_circ_124730,RMVar_hsa_circ_304587,RMVar_hsa_circ_169738,RMVar_hsa_circ_32655 10982 RMVar_ID_10982 Human_SNP_ID_568684042 A-to-I Human chr14 + 105457818 105457818 105457818 CATGGTGTCGGTGCCTGTGGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACCTG CATGGTGTCGGTGCCTGTGGTCCCAGCTACTCCGGAGGCTGAGGCAGGAGAATCGCTTGAACCTG A C MTA1 Ensembl:ENSG00000182979 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1555430203 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14003,RMVar_hsa_circ_39157,RMVar_hsa_circ_10523,RMVar_hsa_circ_63926,RMVar_hsa_circ_169736,RMVar_hsa_circ_124730,RMVar_hsa_circ_304587,RMVar_hsa_circ_169738,RMVar_hsa_circ_32655 10983 RMVar_ID_10983 Human_SNP_ID_240990743 A-to-I Human chr5 - 91299442 91299442 91299442 CTGTAGTCCCCCCTACTTGGGAGGCTGAGTCAAGAGAATCACTTGAACTCGGGAGATGGAAGTTA CTGTAGTCCCCCCTACTTGGGAGGCTGAGTCAGGAGAATCACTTGAACTCGGGAGATGGAAGTTA T C LUCAT1 Ensembl:ENSG00000248323 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956606889 Functional Loss SNV dbSNP153 33..33 33 - - - 10984 RMVar_ID_10984 Human_SNP_ID_240991766 A-to-I Human chr5 - 91303562 91303562 91303562 AAACCCCCTCTCTACTAAAAATACGGAAAATTAGCTGGGTGTGGTGGTGCATGTCTGTAGTCCCA AAACCCCCTCTCTACTAAAAATACGGAAAATTTGCTGGGTGTGGTGGTGCATGTCTGTAGTCCCA T A LUCAT1 Ensembl:ENSG00000248323 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1365753688 Functional Loss SNV dbSNP153 33..33 33 - - - 10985 RMVar_ID_10985 Human_SNP_ID_240991778 A-to-I Human chr5 - 91303603 91303603 91303603 CATGAGGTCAGGAGTTCGAGACCAGCCTCACCAATGTGGCAAAACCCCCTCTCTACTAAAAATAC CATGAGGTCAGGAGTTCGAGACCAGCCTCACCGATGTGGCAAAACCCCCTCTCTACTAAAAATAC T C LUCAT1 Ensembl:ENSG00000248323 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs914650642 Functional Loss SNV dbSNP153 33..33 33 - - - 10986 RMVar_ID_10986 Human_SNP_ID_240992896 A-to-I Human chr5 - 91308407 91308405 91308407 AAAATTAGCCAGGCTTGGTGGCTTGTACCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA AAAATTAGCCAGGCTTGGTGGCTTGTACCTGT__TCCCAGCTACTCAGGAGGCTGAGGCAGGAGA ATT A LUCAT1 Ensembl:ENSG00000248323 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1421688864 Functional Loss DEL dbSNP153 33..34 33 - - - 10987 RMVar_ID_10987 Human_SNP_ID_240993072 A-to-I Human chr5 - 91309082 91309082 91309082 TGAAATCCTCTGTCAAGAAGATATTGTCGGCCAGGGGCGGTGGCTCACACCTGTAATCCCAGCAC TGAAATCCTCTGTCAAGAAGATATTGTCGGCCTGGGGCGGTGGCTCACACCTGTAATCCCAGCAC T A LUCAT1 Ensembl:ENSG00000248323 lincRNA intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1007346369 Functional Loss SNV dbSNP153 33..33 33 - - - 10988 RMVar_ID_10988 Human_SNP_ID_240993167 A-to-I Human chr5 - 91309535 91309535 91309535 TTGAGGCTGTAGTGAGCCATGATTGCCCCACTACACTCCAGCCTGGATGACAGAGTGAGACCCTG TTGAGGCTGTAGTGAGCCATGATTGCCCCACTGCACTCCAGCCTGGATGACAGAGTGAGACCCTG T C LUCAT1 Ensembl:ENSG00000248323 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs554151074 Functional Loss SNV dbSNP153 33..33 33 - - - 10989 RMVar_ID_10989 Human_SNP_ID_240993293 A-to-I Human chr5 - 91310098 91310098 91310098 CTGCCTCGGCCTCGTAACGCGTTAGGATTACAAGCGTGAACACCGCACCTGGCCAGCATGTGGTC CTGCCTCGGCCTCGTAACGCGTTAGGATTACATGCGTGAACACCGCACCTGGCCAGCATGTGGTC T A LUCAT1 Ensembl:ENSG00000248323 lincRNA intron GSE100210;GSE99789;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BERP35T4 cell line - 29129909,29796672,31158229 RNA-Seq:(High) rs1454055151 Functional Loss SNV dbSNP153 33..33 33 - - - 10990 RMVar_ID_10990 Human_SNP_ID_240993294 A-to-I Human chr5 - 91310098 91310098 91310098 CTGCCTCGGCCTCGTAACGCGTTAGGATTACAAGCGTGAACACCGCACCTGGCCAGCATGTGGTC CTGCCTCGGCCTCGTAACGCGTTAGGATTACAGGCGTGAACACCGCACCTGGCCAGCATGTGGTC T C LUCAT1 Ensembl:ENSG00000248323 lincRNA intron GSE100210;GSE99789;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BERP35T4 cell line - 29129909,29796672,31158229 RNA-Seq:(High) rs1454055151 Functional Loss SNV dbSNP153 33..33 33 - - - 10991 RMVar_ID_10991 Human_SNP_ID_240993329 A-to-I Human chr5 - 91310204 91310204 91310204 CTGGGGTGCACCACCACACCCAGCTAATTTTTAAATTTTTTTTTGTAGATATTGTCTCACTCTGT CTGGGGTGCACCACCACACCCAGCTAATTTTTTAATTTTTTTTTGTAGATATTGTCTCACTCTGT T A LUCAT1 Ensembl:ENSG00000248323 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs529214737 Functional Loss SNV dbSNP153 33..33 33 - - - 10992 RMVar_ID_10992 Human_SNP_ID_241013905 A-to-I Human chr5 + 91393758 91393758 91393758 ATGGTGGCACATGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGAAGAATCGCTTGAACCCA ATGGTGGCACATGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGAAGAATCGCTTGAACCCA A G ARRDC3-AS1 Ensembl:ENSG00000281357 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1219086759 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109551,RMVar_hsa_circ_233232 10993 RMVar_ID_10993 Human_SNP_ID_241019790 A-to-I Human chr5 + 91420389 91420388 91420389 CATGTCTTTTGTAGGGACATGGATGAAGCCGGAAACCATCATTCTGAGAAAACTATCGCAAGGAC CATGTCTTTTGTAGGGACATGGATGAAGCCGG_AACCATCATTCTGAGAAAACTATCGCAAGGAC GA G ARRDC3-AS1 Ensembl:ENSG00000281357 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1362380712 Functional Loss DEL dbSNP153 33..33 33 - - - 10994 RMVar_ID_10994 Human_SNP_ID_241221949 A-to-I Human chr5 + 92257542 92257542 92257542 TGGAGCTGGAGGCTGCTATCCTAAGTAAACACAAGAACAGAAACCCAAATTCCCTATGTTCTCAC TGGAGCTGGAGGCTGCTATCCTAAGTAAACACTAGAACAGAAACCCAAATTCCCTATGTTCTCAC A T AC114316.1 Ensembl:ENSG00000250049 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1561302652 Functional Loss SNV dbSNP153 33..33 33 - - - 10995 RMVar_ID_10995 Human_SNP_ID_241375227 A-to-I Human chr5 - 92890595 92890586 92890595 CTTCAATGGACATTGCCAAATACCAAGATGCCAAGGTGGGTGATAGCACCACCTCAGTGACCTTA CTTCAATGGACATTGCCAAATACCAAGATGCC_________GATAGCACCACCTCAGTGACCTTA CACCCACCTT C CCT7P2 Ensembl:ENSG00000249958 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1386146433 Functional Loss DEL dbSNP153 33..41 33 - - - 10996 RMVar_ID_10996 Human_SNP_ID_241554804 A-to-I Human chr5 - 93650909 93650909 93650909 TAGCTCACCGCAGCCTTGATCTCCTGGGTTCAAGCAATCCTCCTGCCTCAGCCTCCCAAGAAGCT TAGCTCACCGCAGCCTTGATCTCCTGGGTTCAGGCAATCCTCCTGCCTCAGCCTCCCAAGAAGCT T C FAM172A Ensembl:ENSG00000113391 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1368717009 Functional Loss SNV dbSNP153 33..33 33 - - - 10997 RMVar_ID_10997 Human_SNP_ID_241645985 A-to-I Human chr5 - 94049815 94049815 94049815 TGATTTTTTAAATTTTGTTTTGTTTTTGAGACAGGGTCTCGCTCTGTTACTCAGGCTGGAGTGCA TGATTTTTTAAATTTTGTTTTGTTTTTGAGACGGGGTCTCGCTCTGTTACTCAGGCTGGAGTGCA T C FAM172A Ensembl:ENSG00000113391 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1391925779 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_233252,RMVar_hsa_circ_74164,RMVar_hsa_circ_233251,RMVar_hsa_circ_35913 10998 RMVar_ID_10998 Human_SNP_ID_241646149 A-to-I Human chr5 - 94050526 94050526 94050526 TTAAAAGTTCCTGTTCAGTGGCTCACGCCTGTAATTACAGCACTCTGGGAGGCCGAGGCAGGTGG TTAAAAGTTCCTGTTCAGTGGCTCACGCCTGTGATTACAGCACTCTGGGAGGCCGAGGCAGGTGG T C FAM172A Ensembl:ENSG00000113391 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs760151711 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_233252,RMVar_hsa_circ_74164,RMVar_hsa_circ_233251,RMVar_hsa_circ_35913 10999 RMVar_ID_10999 Human_SNP_ID_241713629 A-to-I Human chr5 - 94368366 94368366 94368366 GAGTTCGAGACTAGCCTGGGCAACATGCAGAAACCCTATTTCTACAAAAAATACAAAAATTAATT GAGTTCGAGACTAGCCTGGGCAACATGCAGAAGCCCTATTTCTACAAAAAATACAAAAATTAATT T C KIAA0825 Ensembl:ENSG00000185261 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs566217145 Functional Loss SNV dbSNP153 33..33 33 - - - 11000 RMVar_ID_11000 Human_SNP_ID_241719716 A-to-I Human chr5 - 94397439 94397439 94397439 TGTAAAAACTAGGTCCAACACATATTTGAATAATCTTCTAAGGCTGTTGCATTAAATAAGATCAT TGTAAAAACTAGGTCCAACACATATTTGAATAGTCTTCTAAGGCTGTTGCATTAAATAAGATCAT T C KIAA0825 Ensembl:ENSG00000185261 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1360711278 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_334136,RMVar_hsa_circ_339227,RMVar_hsa_circ_345493,RMVar_hsa_circ_366972,RMVar_hsa_circ_342366,RMVar_hsa_circ_338433,RMVar_hsa_circ_301500,RMVar_hsa_circ_312233,RMVar_hsa_circ_291424,RMVar_hsa_circ_295069,RMVar_hsa_circ_291069,RMVar_hsa_circ_42479,RMVar_hsa_circ_233264,RMVar_hsa_circ_233266,RMVar_hsa_circ_233268,RMVar_hsa_circ_233269,RMVar_hsa_circ_233267,RMVar_hsa_circ_233265,RMVar_hsa_circ_233262,RMVar_hsa_circ_233263,RMVar_hsa_circ_67067,RMVar_hsa_circ_346080 11001 RMVar_ID_11001 Human_SNP_ID_241719721 A-to-I Human chr5 - 94397468 94397468 94397468 AAAATTAATTGGAACAGTCTTTATAAGTTTGTAAAAACTAGGTCCAACACATATTTGAATAATCT AAAATTAATTGGAACAGTCTTTATAAGTTTGTGAAAACTAGGTCCAACACATATTTGAATAATCT T C KIAA0825 Ensembl:ENSG00000185261 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1038632434 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_334136,RMVar_hsa_circ_339227,RMVar_hsa_circ_345493,RMVar_hsa_circ_366972,RMVar_hsa_circ_342366,RMVar_hsa_circ_338433,RMVar_hsa_circ_301500,RMVar_hsa_circ_312233,RMVar_hsa_circ_291424,RMVar_hsa_circ_295069,RMVar_hsa_circ_291069,RMVar_hsa_circ_42479,RMVar_hsa_circ_233264,RMVar_hsa_circ_233266,RMVar_hsa_circ_233268,RMVar_hsa_circ_233269,RMVar_hsa_circ_233267,RMVar_hsa_circ_233265,RMVar_hsa_circ_233262,RMVar_hsa_circ_233263,RMVar_hsa_circ_67067,RMVar_hsa_circ_346080 11002 RMVar_ID_11002 Human_SNP_ID_241719994 A-to-I Human chr5 - 94399033 94399033 94399033 CTTAGGAGATTGTTCAAATATGTGTTGGATCTAGTTTTTACAAACTTATAAAGACTGCTCCAATT CTTAGGAGATTGTTCAAATATGTGTTGGATCTTGTTTTTACAAACTTATAAAGACTGCTCCAATT T A KIAA0825 Ensembl:ENSG00000185261 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs949135376 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_334136,RMVar_hsa_circ_339227,RMVar_hsa_circ_345493,RMVar_hsa_circ_366972,RMVar_hsa_circ_342366,RMVar_hsa_circ_338433,RMVar_hsa_circ_301500,RMVar_hsa_circ_312233,RMVar_hsa_circ_291424,RMVar_hsa_circ_295069,RMVar_hsa_circ_291069,RMVar_hsa_circ_42479,RMVar_hsa_circ_233264,RMVar_hsa_circ_233266,RMVar_hsa_circ_233268,RMVar_hsa_circ_233269,RMVar_hsa_circ_233267,RMVar_hsa_circ_233265,RMVar_hsa_circ_233262,RMVar_hsa_circ_233263,RMVar_hsa_circ_67067,RMVar_hsa_circ_346080 11003 RMVar_ID_11003 Human_SNP_ID_241722844 A-to-I Human chr5 - 94413241 94413241 94413241 CCTTCTTAAAAAATCCATATACTCGGCCAAGCATGGTGGCTCACGCCTGTAATCCCAGCACTTTG CCTTCTTAAAAAATCCATATACTCGGCCAAGCGTGGTGGCTCACGCCTGTAATCCCAGCACTTTG T C KIAA0825 Ensembl:ENSG00000185261 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs950373074 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_334136,RMVar_hsa_circ_339227,RMVar_hsa_circ_345493,RMVar_hsa_circ_366972,RMVar_hsa_circ_342366,RMVar_hsa_circ_338433,RMVar_hsa_circ_301500,RMVar_hsa_circ_312233,RMVar_hsa_circ_291424,RMVar_hsa_circ_295069,RMVar_hsa_circ_42479,RMVar_hsa_circ_233264,RMVar_hsa_circ_233266,RMVar_hsa_circ_233268,RMVar_hsa_circ_233267,RMVar_hsa_circ_233265,RMVar_hsa_circ_233262,RMVar_hsa_circ_233263,RMVar_hsa_circ_67067,RMVar_hsa_circ_346080,RMVar_hsa_circ_52392,RMVar_hsa_circ_337335 11004 RMVar_ID_11004 Human_SNP_ID_241757475 A-to-I Human chr5 - 94569196 94569196 94569196 GAGGCATGGGGGTCAGGGATTGAGGTCTTGGTAAGTGTTTTAGTGGGATTAGCAATAGAAGTGGG GAGGCATGGGGGTCAGGGATTGAGGTCTTGGTGAGTGTTTTAGTGGGATTAGCAATAGAAGTGGG T C KIAA0825,MTND6P3 Ensembl:ENSG00000185261,Ensembl:ENSG00000254132 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs796493858 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_345493,RMVar_hsa_circ_330666,RMVar_hsa_circ_308880,RMVar_hsa_circ_233278 11005 RMVar_ID_11005 Human_SNP_ID_241784183 A-to-I Human chr5 + 94677275 94677275 94677275 ACACCTTTGATTTAAATATAAACATTTTTTCGAAACATTAAAACCAGCTGAAATTCCTGTTACTT ACACCTTTGATTTAAATATAAACATTTTTTCGGAACATTAAAACCAGCTGAAATTCCTGTTACTT A G SLF1 Ensembl:ENSG00000133302 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1019771380 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_341114,RMVar_hsa_circ_308369,RMVar_hsa_circ_233281,RMVar_hsa_circ_45913,RMVar_hsa_circ_68668,RMVar_hsa_circ_102015,RMVar_hsa_circ_233292,RMVar_hsa_circ_42836,RMVar_hsa_circ_50588,RMVar_hsa_circ_369864,RMVar_hsa_circ_233295,RMVar_hsa_circ_2443,RMVar_hsa_circ_270610,RMVar_hsa_circ_33951,RMVar_hsa_circ_304218,RMVar_hsa_circ_347295,RMVar_hsa_circ_233297,RMVar_hsa_circ_339609,RMVar_hsa_circ_340786 11006 RMVar_ID_11006 Human_SNP_ID_241784294 A-to-I Human chr5 + 94677735 94677735 94677735 AATGCTTTGAAAAAGTGTTTATATTTCAATCAAAGGTGTTTTTAAAATTTCATTTTCACACTTCT AATGCTTTGAAAAAGTGTTTATATTTCAATCATAGGTGTTTTTAAAATTTCATTTTCACACTTCT A T SLF1 Ensembl:ENSG00000133302 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1410800379 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7487689,Human_RBP_ID_15547871 RMVar_hsa_circ_341114,RMVar_hsa_circ_308369,RMVar_hsa_circ_233281,RMVar_hsa_circ_45913,RMVar_hsa_circ_68668,RMVar_hsa_circ_102015,RMVar_hsa_circ_233292,RMVar_hsa_circ_42836,RMVar_hsa_circ_50588,RMVar_hsa_circ_369864,RMVar_hsa_circ_233295,RMVar_hsa_circ_2443,RMVar_hsa_circ_270610,RMVar_hsa_circ_33951,RMVar_hsa_circ_304218,RMVar_hsa_circ_347295,RMVar_hsa_circ_233297,RMVar_hsa_circ_339609,RMVar_hsa_circ_340786 11007 RMVar_ID_11007 Human_SNP_ID_241785142 A-to-I Human chr5 + 94680942 94680942 94680942 GTCACAGATTATTTTGCTCCCAAAGATCTATTAATATATTTGATCACTAACATTCAAAACTTTCG GTCACAGATTATTTTGCTCCCAAAGATCTATTGATATATTTGATCACTAACATTCAAAACTTTCG A G SLF1 Ensembl:ENSG00000133302 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1443042561 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_341114,RMVar_hsa_circ_45913,RMVar_hsa_circ_102015,RMVar_hsa_circ_233292,RMVar_hsa_circ_2443,RMVar_hsa_circ_33951,RMVar_hsa_circ_304218 11008 RMVar_ID_11008 Human_SNP_ID_241785156 A-to-I Human chr5 + 94681005 94681005 94681005 CGATGAGACTTAAATTGTCACTATTGAAAAGTACTTTTAAGCCTTTTTCTTTACCTTTCTCAAAA CGATGAGACTTAAATTGTCACTATTGAAAAGTGCTTTTAAGCCTTTTTCTTTACCTTTCTCAAAA A G SLF1 Ensembl:ENSG00000133302 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1045136714 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15547943 RMVar_hsa_circ_341114,RMVar_hsa_circ_45913,RMVar_hsa_circ_102015,RMVar_hsa_circ_233292,RMVar_hsa_circ_2443,RMVar_hsa_circ_33951,RMVar_hsa_circ_304218 11009 RMVar_ID_11009 Human_SNP_ID_241785182 A-to-I Human chr5 + 94681111 94681110 94681112 AGGCTTCAAATTCGGTTATAGCTAGGCAGTTTAAAAGTTTTAAACATTATTTCTTTTGTCTTTTT AGGCTTCAAATTCGGTTATAGCTAGGCAGTTT__AAGTTTTAAACATTATTTCTTTTGTCTTTTT TAA T SLF1 Ensembl:ENSG00000133302 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965484410 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_341114,RMVar_hsa_circ_45913,RMVar_hsa_circ_102015,RMVar_hsa_circ_233292,RMVar_hsa_circ_2443,RMVar_hsa_circ_33951,RMVar_hsa_circ_304218 11010 RMVar_ID_11010 Human_SNP_ID_241785507 A-to-I Human chr5 + 94682177 94682177 94682177 CAAATATATTAATAGATCTTTGAGAGCAAAATAATCCATCAACAGGATTATAACAGTAACACTAA CAAATATATTAATAGATCTTTGAGAGCAAAATCATCCATCAACAGGATTATAACAGTAACACTAA A C SLF1 Ensembl:ENSG00000133302 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1561471387 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10229769 RMVar_hsa_circ_341114,RMVar_hsa_circ_45913,RMVar_hsa_circ_102015,RMVar_hsa_circ_233292,RMVar_hsa_circ_2443,RMVar_hsa_circ_33951,RMVar_hsa_circ_304218 11011 RMVar_ID_11011 Human_SNP_ID_241901004 A-to-I Human chr5 - 95180448 95180448 95180448 GTGAAGAAGGAGGAAGCTTTCAGCTTTGGTCAAAATGCTCCTAAGAGGTCAAGTAGTGTGGACTA GTGAAGAAGGAGGAAGCTTTCAGCTTTGGTCACAATGCTCCTAAGAGGTCAAGTAGTGTGGACTA T G MCTP1 Ensembl:ENSG00000175471 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1473648639 Functional Loss SNV dbSNP153 33..33 33 - - - 11012 RMVar_ID_11012 Human_SNP_ID_241906262 A-to-I Human chr5 - 95203900 95203900 95203900 AATGTTTCTTGAAGATGACTAGATCTAAAATGATAAATATTGAATATCCTGGCAATTAGGAAGAG AATGTTTCTTGAAGATGACTAGATCTAAAATGCTAAATATTGAATATCCTGGCAATTAGGAAGAG T G MCTP1 Ensembl:ENSG00000175471 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs995809186 Functional Loss SNV dbSNP153 33..33 33 - - - 11013 RMVar_ID_11013 Human_SNP_ID_241982559 A-to-I Human chr5 - 95530147 95530147 95530147 GATTCAAAAAGTGGTCCAGGCCTCATTGGCTTAGGCATTAAAGCATTACAAGACAAAAAGTATGA GATTCAAAAAGTGGTCCAGGCCTCATTGGCTTTGGCATTAAAGCATTACAAGACAAAAAGTATGA T A TTC37 Ensembl:ENSG00000198677 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1427746198 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_648664,Human_RBP_ID_2953606,Human_RBP_ID_18849681,Human_RBP_ID_24122790,Human_RBP_ID_27825603 Human_Splice_Rec_674644,Human_Splice_Rec_674645,Human_Splice_Rec_674728,Human_Splice_Rec_674729,Human_Splice_Rec_674892,Human_Splice_Rec_674893,Human_Splice_Rec_674916,Human_Splice_Rec_674917 Human_miRNA_ID_360750,Human_miRNA_ID_1265919,Human_miRNA_ID_2096221 RMVar_hsa_circ_88669,RMVar_hsa_circ_233333,RMVar_hsa_circ_95131,RMVar_hsa_circ_233337,RMVar_hsa_circ_104951,RMVar_hsa_circ_2479,RMVar_hsa_circ_233352,RMVar_hsa_circ_233355,RMVar_hsa_circ_115353,RMVar_hsa_circ_233357,RMVar_hsa_circ_57008,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 11014 RMVar_ID_11014 Human_SNP_ID_241999772 A-to-I Human chr5 - 95608778 95608778 95608778 CTCCTGGCTCAGCCGCCCAAGTAGCTGGGACTATAGGCATGCGCCACCACACCTGGCTAATTTTT CTCCTGGCTCAGCCGCCCAAGTAGCTGGGACTGTAGGCATGCGCCACCACACCTGGCTAATTTTT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941335811 Functional Loss SNV dbSNP153 33..33 33 - - - 11015 RMVar_ID_11015 Human_SNP_ID_242039915 A-to-I Human chr5 + 95783324 95783324 95783324 TTTTTTATTTTTAGTAGAGATGAGGTTTCACCATGTCCGCCAGGATGGACTTGATTTCTTGACCT TTTTTTATTTTTAGTAGAGATGAGGTTTCACCGTGTCCGCCAGGATGGACTTGATTTCTTGACCT A G RHOBTB3 Ensembl:ENSG00000164292 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1322825311 Functional Loss SNV dbSNP153 33..33 33 - - - 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_233374,RMVar_hsa_circ_233373,RMVar_hsa_circ_289185,RMVar_hsa_circ_271944,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_233398,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 11016 RMVar_ID_11016 Human_SNP_ID_242039984 A-to-I Human chr5 + 95783544 95783544 95783544 GCTCAGGAGTTCAAGACCAGCCTGGGCAACATAGTGAGACCTGTCTCTACAAAAAAAAAAAAAAA GCTCAGGAGTTCAAGACCAGCCTGGGCAACATTGTGAGACCTGTCTCTACAAAAAAAAAAAAAAA A T RHOBTB3 Ensembl:ENSG00000164292 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1160334843 Functional Loss SNV dbSNP153 33..33 33 - - - 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_233374,RMVar_hsa_circ_233373,RMVar_hsa_circ_289185,RMVar_hsa_circ_271944,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_233398,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 11017 RMVar_ID_11017 Human_SNP_ID_242041877 A-to-I Human chr5 + 95791807 95791807 95791807 ACCTCAAATAATCCGCCCGCCTCGGCCTCCCAAAGTGGTGGGATTACAGACATGAGCCATCGTGC ACCTCAAATAATCCGCCCGCCTCGGCCTCCCAGAGTGGTGGGATTACAGACATGAGCCATCGTGC A G RHOBTB3 Ensembl:ENSG00000164292 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1234036459 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76091,RMVar_hsa_circ_233387,RMVar_hsa_circ_111348,RMVar_hsa_circ_233390,RMVar_hsa_circ_117059,RMVar_hsa_circ_233405 11018 RMVar_ID_11018 Human_SNP_ID_242065151 A-to-I Human chr5 - 95892350 95892350 95892350 TTGGGGCCAGGGGTTCGAGACCAGACTGGGCAACATGACGAAACCCTGTCTCTACTAAAAATACA TTGGGGCCAGGGGTTCGAGACCAGACTGGGCACCATGACGAAACCCTGTCTCTACTAAAAATACA T G ELL2 Ensembl:ENSG00000118985 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1008522031 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112317,RMVar_hsa_circ_50826,RMVar_hsa_circ_233408 11019 RMVar_ID_11019 Human_SNP_ID_242065154 A-to-I Human chr5 - 95892360 95892360 95892360 GGTGGATCACTTGGGGCCAGGGGTTCGAGACCAGACTGGGCAACATGACGAAACCCTGTCTCTAC GGTGGATCACTTGGGGCCAGGGGTTCGAGACCGGACTGGGCAACATGACGAAACCCTGTCTCTAC T C ELL2 Ensembl:ENSG00000118985 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1252140509 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112317,RMVar_hsa_circ_50826,RMVar_hsa_circ_233408 11020 RMVar_ID_11020 Human_SNP_ID_242065570 A-to-I Human chr5 - 95894239 95894233 95894240 TCATTAGTTAATCCCCCCTTTTTTTGTTTTTGAGACGGAATTTCGCTCTTGTTGCCCAGGCTGGA TCATTAGTTAATCCCCCCTTTTTTTGTTTTT_______AATTTCGCTCTTGTTGCCCAGGCTGGA TCCGTCTC T ELL2 Ensembl:ENSG00000118985 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1438714771 Functional Loss DEL dbSNP153 32..38 33 - - - RMVar_hsa_circ_112317,RMVar_hsa_circ_50826,RMVar_hsa_circ_233408 11021 RMVar_ID_11021 Human_SNP_ID_242070150 A-to-I Human chr5 - 95914726 95914718 95914727 ACCCTCCCACTTCAGTCTCCTGACTAGCTGGAACTTCAGGCACACGCCACCATGCCCAGCTAATT ACCCTCCCACTTCAGTCTCCTGACTAGCTGG_________CACACGCCACCATGCCCAGCTAATT GCCTGAAGTT G ELL2 Ensembl:ENSG00000118985 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1368271126 Functional Loss DEL dbSNP153 32..40 33 - - - RMVar_hsa_circ_50826,RMVar_hsa_circ_352960,RMVar_hsa_circ_57695,RMVar_hsa_circ_233410,RMVar_hsa_circ_27913,RMVar_hsa_circ_273902,RMVar_hsa_circ_359020,RMVar_hsa_circ_118079,RMVar_hsa_circ_233411,RMVar_hsa_circ_291008,RMVar_hsa_circ_342847,RMVar_hsa_circ_233412 11022 RMVar_ID_11022 Human_SNP_ID_242070151 A-to-I Human chr5 - 95914726 95914726 95914726 ACCCTCCCACTTCAGTCTCCTGACTAGCTGGAACTTCAGGCACACGCCACCATGCCCAGCTAATT ACCCTCCCACTTCAGTCTCCTGACTAGCTGGACCTTCAGGCACACGCCACCATGCCCAGCTAATT T G ELL2 Ensembl:ENSG00000118985 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1309492851 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50826,RMVar_hsa_circ_352960,RMVar_hsa_circ_57695,RMVar_hsa_circ_233410,RMVar_hsa_circ_27913,RMVar_hsa_circ_273902,RMVar_hsa_circ_359020,RMVar_hsa_circ_118079,RMVar_hsa_circ_233411,RMVar_hsa_circ_291008,RMVar_hsa_circ_342847,RMVar_hsa_circ_233412 11023 RMVar_ID_11023 Human_SNP_ID_242111804 A-to-I Human chr5 + 96101022 96101022 96101022 ATAACTCACTGTAATTTCAAACTCCTGGGCTCAAGCAGTTCTTCTGCCTCAGCCATTGGGACCAT ATAACTCACTGTAATTTCAAACTCCTGGGCTCCAGCAGTTCTTCTGCCTCAGCCATTGGGACCAT A C AC104123.1,MIR583HG Ensembl:ENSG00000251314,Ensembl:ENSG00000250551 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs953500040 Functional Loss SNV dbSNP153 33..33 33 - - - 11024 RMVar_ID_11024 Human_SNP_ID_242246831 A-to-I Human chr5 + 96664476 96664476 96664476 TACAGGGTCTCTCTCACTATGTTGCCCAGGCTAGTCTAAAACTCCTGGTCTCAAGCAATCCTCCC TACAGGGTCTCTCTCACTATGTTGCCCAGGCTGGTCTAAAACTCCTGGTCTCAAGCAATCCTCCC A G CAST Ensembl:ENSG00000153113 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs552261116 Functional Loss SNV dbSNP153 33..33 33 - - - 11025 RMVar_ID_11025 Human_SNP_ID_242263410 A-to-I Human chr5 + 96737904 96737904 96737904 TGACTTAATAGATACTTTAGGAGGACCTGAAGAAACTGAAGAAGAAAATACAACGTATACTGGAC TGACTTAATAGATACTTTAGGAGGACCTGAAGGAACTGAAGAAGAAAATACAACGTATACTGGAC A G CAST Ensembl:ENSG00000153113 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs765136385 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_75940,Human_RBP_ID_945935,Human_RBP_ID_2002374,Human_RBP_ID_3967324,Human_RBP_ID_5617247,Human_RBP_ID_7489723,Human_RBP_ID_8236939,Human_RBP_ID_9398013,Human_RBP_ID_15551588,Human_RBP_ID_18413690,Human_RBP_ID_18538152,Human_RBP_ID_19124572,Human_RBP_ID_22099516,Human_RBP_ID_24123148,Human_RBP_ID_24547972,Human_RBP_ID_26350518,Human_RBP_ID_27517883,Human_RBP_ID_27825615 Human_Splice_Rec_675440,Human_Splice_Rec_675441,Human_Splice_Rec_675462,Human_Splice_Rec_675463,Human_Splice_Rec_675524,Human_Splice_Rec_675525,Human_Splice_Rec_675582,Human_Splice_Rec_675583,Human_Splice_Rec_675608,Human_Splice_Rec_675609,Human_Splice_Rec_675680,Human_Splice_Rec_675681,Human_Splice_Rec_675704,Human_Splice_Rec_675705,Human_Splice_Rec_675764,Human_Splice_Rec_675765,Human_Splice_Rec_675830,Human_Splice_Rec_675831,Human_Splice_Rec_675888,Human_Splice_Rec_675889,Human_Splice_Rec_675948,Human_Splice_Rec_675949,Human_Splice_Rec_676006,Human_Splice_Rec_676007,Human_Splice_Rec_676062,Human_Splice_Rec_676063,Human_Splice_Rec_676120,Human_Splice_Rec_676121,Human_Splice_Rec_676182,Human_Splice_Rec_676183,Human_Splice_Rec_676236,Human_Splice_Rec_676237,Human_Splice_Rec_676288,Human_Splice_Rec_676289,Human_Splice_Rec_676332,Human_Splice_Rec_676333,Human_Splice_Rec_676366,Human_Splice_Rec_676367,Human_Splice_Rec_676378,Human_Splice_Rec_676379,Human_Splice_Rec_676422,Human_Splice_Rec_676423 RMVar_hsa_circ_14318,RMVar_hsa_circ_233414,RMVar_hsa_circ_83633,RMVar_hsa_circ_53712,RMVar_hsa_circ_347412,RMVar_hsa_circ_233419,RMVar_hsa_circ_103172 11026 RMVar_ID_11026 Human_SNP_ID_242272260 A-to-I Human chr5 - 96774786 96774786 96774786 AATAGGTATAAAAGTGGAATTGGAATTTTTATACTTATTTGTTGTAGTGAATGGTTTAATAAAAA AATAGGTATAAAAGTGGAATTGGAATTTTTATGCTTATTTGTTGTAGTGAATGGTTTAATAAAAA T C ERAP1 Ensembl:ENSG00000164307 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1003038016 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_995993 11027 RMVar_ID_11027 Human_SNP_ID_242272277 A-to-I Human chr5 - 96774840 96774840 96774840 AGTGACTTCTGGACATAAATCTGCCATTTATTAAACCATTCACTACAACAAATAAATAGGTATAA AGTGACTTCTGGACATAAATCTGCCATTTATTGAACCATTCACTACAACAAATAAATAGGTATAA T C ERAP1 Ensembl:ENSG00000164307 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs7861 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26529169,Human_RBP_ID_27517889 Human_miRNA_ID_737150 11028 RMVar_ID_11028 Human_SNP_ID_242335447 A-to-I Human chr5 + 97031897 97031896 97031897 ACAAAGCGAGACTGTCTCAAAAAACAAAAAACAAAAAAAAAAGAGTTAAGTGTTGATTTTGTTGG ACAAAGCGAGACTGTCTCAAAAAACAAAAAAC_AAAAAAAAAGAGTTAAGTGTTGATTTTGTTGG CA C LNPEP Ensembl:ENSG00000113441 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs149987000 Functional Loss DEL dbSNP153 33..33 33 - - - 11029 RMVar_ID_11029 Human_SNP_ID_242800399 A-to-I Human chr5 - 98862035 98862035 98862035 CTTCCACCTCAGTCTCTTTGGTAGCTGGGACTACAGGCCCACGCTACCAGGCCTGGCTAATTCTT CTTCCACCTCAGTCTCTTTGGTAGCTGGGACTGCAGGCCCACGCTACCAGGCCTGGCTAATTCTT T C CHD1 Ensembl:ENSG00000153922 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs867197074 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4420,RMVar_hsa_circ_265678 11030 RMVar_ID_11030 Human_SNP_ID_242801954 A-to-I Human chr5 - 98868179 98868179 98868179 GGGACTAGAGGCATGTGCCATATACCCAGCTAATTTTTAGTTTTTTGTAAAGATGGGGATTTTTT GGGACTAGAGGCATGTGCCATATACCCAGCTACTTTTTAGTTTTTTGTAAAGATGGGGATTTTTT T G CHD1 Ensembl:ENSG00000153922 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1315831225 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4420,RMVar_hsa_circ_265678,RMVar_hsa_circ_63274,RMVar_hsa_circ_92158,RMVar_hsa_circ_233463 11031 RMVar_ID_11031 Human_SNP_ID_242808181 A-to-I Human chr5 - 98891727 98891727 98891727 GGCTCACTGCAACCTCCACCTTCTGGTTTCAAATGATTCTGGTGCCTCAGCCTCCCAAGTAGCTG GGCTCACTGCAACCTCCACCTTCTGGTTTCAATTGATTCTGGTGCCTCAGCCTCCCAAGTAGCTG T A CHD1 Ensembl:ENSG00000153922 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs545192156 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265678,RMVar_hsa_circ_92158,RMVar_hsa_circ_233463,RMVar_hsa_circ_356817,RMVar_hsa_circ_32549,RMVar_hsa_circ_233466,RMVar_hsa_circ_327429,RMVar_hsa_circ_46459,RMVar_hsa_circ_9122,RMVar_hsa_circ_233468,RMVar_hsa_circ_233469,RMVar_hsa_circ_267197,RMVar_hsa_circ_25755,RMVar_hsa_circ_318278,RMVar_hsa_circ_57654,RMVar_hsa_circ_233475,RMVar_hsa_circ_329085,RMVar_hsa_circ_59199,RMVar_hsa_circ_69254,RMVar_hsa_circ_266555,RMVar_hsa_circ_233476,RMVar_hsa_circ_66525,RMVar_hsa_circ_326467 11032 RMVar_ID_11032 Human_SNP_ID_242808993 A-to-I Human chr5 - 98895053 98895052 98895053 GCTTTGGGAGGCCAAGGTAGGTGGATCATCTGAGGCTGGGAGTTCGAGACCAGTCTGACCAACAT GCTTTGGGAGGCCAAGGTAGGTGGATCATCTG_GGCTGGGAGTTCGAGACCAGTCTGACCAACAT CT C CHD1 Ensembl:ENSG00000153922 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1353620381 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_8625794 RMVar_hsa_circ_265678,RMVar_hsa_circ_92158,RMVar_hsa_circ_233463,RMVar_hsa_circ_356817,RMVar_hsa_circ_233466,RMVar_hsa_circ_46459,RMVar_hsa_circ_233468,RMVar_hsa_circ_267197,RMVar_hsa_circ_57654,RMVar_hsa_circ_59199,RMVar_hsa_circ_69254,RMVar_hsa_circ_66525,RMVar_hsa_circ_14438,RMVar_hsa_circ_107550,RMVar_hsa_circ_344830,RMVar_hsa_circ_366298,RMVar_hsa_circ_71026,RMVar_hsa_circ_90726,RMVar_hsa_circ_34851,RMVar_hsa_circ_68676,RMVar_hsa_circ_233478,RMVar_hsa_circ_233479,RMVar_hsa_circ_233480,RMVar_hsa_circ_266553 11033 RMVar_ID_11033 Human_SNP_ID_242816904 A-to-I Human chr5 - 98924071 98924071 98924071 TAAAATTTTTTGTAGAGATGAGGTCTCACCATATTGCCTCAGCTGGTCTTGAACTCATGGGCTCA TAAAATTTTTTGTAGAGATGAGGTCTCACCATGTTGCCTCAGCTGGTCTTGAACTCATGGGCTCA T C CHD1 Ensembl:ENSG00000153922 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs535600352 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15554470 RMVar_hsa_circ_366298 11034 RMVar_ID_11034 Human_SNP_ID_242816905 A-to-I Human chr5 - 98924071 98924071 98924071 TAAAATTTTTTGTAGAGATGAGGTCTCACCATATTGCCTCAGCTGGTCTTGAACTCATGGGCTCA TAAAATTTTTTGTAGAGATGAGGTCTCACCATCTTGCCTCAGCTGGTCTTGAACTCATGGGCTCA T G CHD1 Ensembl:ENSG00000153922 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs535600352 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15554470 RMVar_hsa_circ_366298 11035 RMVar_ID_11035 Human_SNP_ID_242816928 A-to-I Human chr5 - 98924163 98924163 98924163 CACTGCAGCCTCTGCCTCCACCTCCTGGGCTCAAACGATTCTCCCACCTCAGCATCCTGAAAGGC CACTGCAGCCTCTGCCTCCACCTCCTGGGCTCCAACGATTCTCCCACCTCAGCATCCTGAAAGGC T G CHD1 Ensembl:ENSG00000153922 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs969145835 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15554474 RMVar_hsa_circ_366298 11036 RMVar_ID_11036 Human_SNP_ID_242816948 A-to-I Human chr5 - 98924245 98924245 98924245 AATTTTTTTTTTCTTTTCTTTTCTTTTGAGACAGGGCCTCACTCTGTCACCCAGGCTGGAGTACA AATTTTTTTTTTCTTTTCTTTTCTTTTGAGACGGGGCCTCACTCTGTCACCCAGGCTGGAGTACA T C CHD1 Ensembl:ENSG00000153922 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs866304601 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7491511 RMVar_hsa_circ_366298 11037 RMVar_ID_11037 Human_SNP_ID_242823964 A-to-I Human chr5 + 98951525 98951524 98951525 AGCAGCACACCATTATGTAGTAATCCCACCACAGGGATACAGTAGATACAATGCACAGATGTAAA AGCAGCACACCATTATGTAGTAATCCCACCAC_GGGATACAGTAGATACAATGCACAGATGTAAA CA C LINC02062 Ensembl:ENSG00000248489 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1478444804 Functional Loss DEL dbSNP153 33..33 33 - - - 11038 RMVar_ID_11038 Human_SNP_ID_242829060 A-to-I Human chr5 + 98972503 98972503 98972503 CACCTCCCGGGTTCAAGCAATTCTTCTGCGTCAGCCTCCCGAGTAGCTGAGATTACAGGCATGGG CACCTCCCGGGTTCAAGCAATTCTTCTGCGTCCGCCTCCCGAGTAGCTGAGATTACAGGCATGGG A C LINC02062 Ensembl:ENSG00000248489 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1421446826 Functional Loss SNV dbSNP153 33..33 33 - - - 11039 RMVar_ID_11039 Human_SNP_ID_243306695 A-to-I Human chr5 - 100849525 100849525 100849525 CATCCGCCTTAGCCTCCCAAAGTGCGGGGATTACAGGCGTGAGCCACCGCGCTCAGCCAGCAGTG CATCCGCCTTAGCCTCCCAAAGTGCGGGGATTTCAGGCGTGAGCCACCGCGCTCAGCCAGCAGTG T A ST8SIA4 Ensembl:ENSG00000113532 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs141447572 Functional Loss SNV dbSNP153 33..33 33 - - - 11040 RMVar_ID_11040 Human_SNP_ID_243306696 A-to-I Human chr5 - 100849525 100849525 100849525 CATCCGCCTTAGCCTCCCAAAGTGCGGGGATTACAGGCGTGAGCCACCGCGCTCAGCCAGCAGTG CATCCGCCTTAGCCTCCCAAAGTGCGGGGATTGCAGGCGTGAGCCACCGCGCTCAGCCAGCAGTG T C ST8SIA4 Ensembl:ENSG00000113532 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs141447572 Functional Loss SNV dbSNP153 33..33 33 - - - 11041 RMVar_ID_11041 Human_SNP_ID_243307431 A-to-I Human chr5 - 100852260 100852260 100852260 AAAAAGAGCCAGATGTGGTGGCACACACCTGTAGTCCCCGCTACTTGGCAGGCTGAGGCAGGAGA AAAAAGAGCCAGATGTGGTGGCACACACCTGTCGTCCCCGCTACTTGGCAGGCTGAGGCAGGAGA T G ST8SIA4 Ensembl:ENSG00000113532 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs576640155 Functional Loss SNV dbSNP153 33..33 33 - - - 11042 RMVar_ID_11042 Human_SNP_ID_243307440 A-to-I Human chr5 - 100852304 100852304 100852304 GAGCCTGGCCAACATGGCGAAACCCCGCCTCTACTAAAAATACGAAAAAGAGCCAGATGTGGTGG GAGCCTGGCCAACATGGCGAAACCCCGCCTCTGCTAAAAATACGAAAAAGAGCCAGATGTGGTGG T C ST8SIA4 Ensembl:ENSG00000113532 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs925971636 Functional Loss SNV dbSNP153 33..33 33 - - - 11043 RMVar_ID_11043 Human_SNP_ID_243308004 A-to-I Human chr5 - 100854577 100854577 100854577 GTTTTGTTTTGTTTTGTTTTGTTTTTTGAGACAGAGTCTCACTCTGTTGCCCAGGCCGGAGTGCA GTTTTGTTTTGTTTTGTTTTGTTTTTTGAGACGGAGTCTCACTCTGTTGCCCAGGCCGGAGTGCA T C ST8SIA4 Ensembl:ENSG00000113532 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1454541469 Functional Loss SNV dbSNP153 33..33 33 - - - 11044 RMVar_ID_11044 Human_SNP_ID_243310154 A-to-I Human chr5 - 100864475 100864475 100864475 CAACTCCCAGGTTCACGCCATTCTCCTGCCTCAGCCTCCCAAGTGGCTGGGACTGCAGGCGCCCG CAACTCCCAGGTTCACGCCATTCTCCTGCCTCGGCCTCCCAAGTGGCTGGGACTGCAGGCGCCCG T C ST8SIA4 Ensembl:ENSG00000113532 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992110140 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_166888 RMVar_hsa_circ_233489,RMVar_hsa_circ_283703,RMVar_hsa_circ_354422 11045 RMVar_ID_11045 Human_SNP_ID_243840227 A-to-I Human chr5 + 102972335 102972335 102972335 ATGAGGTCTGTCTCTGTCACTCAGGCTGGAGTACCGTGGCGTGATCATAGCTCACTGCAGCCTTG ATGAGGTCTGTCTCTGTCACTCAGGCTGGAGTTCCGTGGCGTGATCATAGCTCACTGCAGCCTTG A T PAM Ensembl:ENSG00000145730 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs967272780 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17575444 RMVar_hsa_circ_12010,RMVar_hsa_circ_23488,RMVar_hsa_circ_330992,RMVar_hsa_circ_18246,RMVar_hsa_circ_366169,RMVar_hsa_circ_334305,RMVar_hsa_circ_36838,RMVar_hsa_circ_233505,RMVar_hsa_circ_29451 11046 RMVar_ID_11046 Human_SNP_ID_243869477 A-to-I Human chr5 - 103092294 103092294 103092294 TTATTCCTTAAAACAACATTAAGGCTGGGCACAGTGGCTTATGCCTGTAATCCCAGCATTTTGAG TTATTCCTTAAAACAACATTAAGGCTGGGCACGGTGGCTTATGCCTGTAATCCCAGCATTTTGAG T C GIN1 Ensembl:ENSG00000145723 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1330405776 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_233513,RMVar_hsa_circ_76717,RMVar_hsa_circ_233512,RMVar_hsa_circ_233514 11047 RMVar_ID_11047 Human_SNP_ID_243894368 A-to-I Human chr5 + 103196947 103196947 103196947 ATCAACCAGGAAAGTAGAAGGATCAGAGAAACAGAAAGAATATCATGATAGAGTAATATCTTGGA ATCAACCAGGAAAGTAGAAGGATCAGAGAAACGGAAAGAATATCATGATAGAGTAATATCTTGGA A G PPIP5K2 Ensembl:ENSG00000145725 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs138867150 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_233541,RMVar_hsa_circ_109333,RMVar_hsa_circ_233539 11048 RMVar_ID_11048 Human_SNP_ID_243894369 A-to-I Human chr5 + 103196949 103196949 103196949 CAACCAGGAAAGTAGAAGGATCAGAGAAACAGAAAGAATATCATGATAGAGTAATATCTTGGAAG CAACCAGGAAAGTAGAAGGATCAGAGAAACAGGAAGAATATCATGATAGAGTAATATCTTGGAAG A G PPIP5K2 Ensembl:ENSG00000145725 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs898958017 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_233541,RMVar_hsa_circ_109333,RMVar_hsa_circ_233539 11049 RMVar_ID_11049 Human_SNP_ID_244134139 A-to-I Human chr5 + 104110776 104110776 104110776 ATGAGCACTTTTAATTTTTTCCCCTTATATTCAATTGCTTTCTGATGGCCCAATCTTTAATGTAT ATGAGCACTTTTAATTTTTTCCCCTTATATTCCATTGCTTTCTGATGGCCCAATCTTTAATGTAT A C LINC02163 Ensembl:ENSG00000251026 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs13190023 Functional Loss SNV dbSNP153 33..33 33 - - - 11050 RMVar_ID_11050 Human_SNP_ID_244163809 A-to-I Human chr5 + 104222520 104222520 104222520 TTTTTTTTTTTTTTTTTTTCAGTCAGAGTCTCACTCTGCCACCCAGCCTGGAGTGCAGTACCTGT TTTTTTTTTTTTTTTTTTTCAGTCAGAGTCTCCCTCTGCCACCCAGCCTGGAGTGCAGTACCTGT A C LINC02163 Ensembl:ENSG00000251026 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1399245369 Functional Loss SNV dbSNP153 33..33 33 - - - 11051 RMVar_ID_11051 Human_SNP_ID_29953165 A-to-I Human chr1 - 120322783 120322783 120322783 CCACGCCCAACCAATTTTTGTATTTTTAGTTGAGATGGGGTTTCACCATGTTGGCCAGGATGGTC CCACGCCCAACCAATTTTTGTATTTTTAGTTGGGATGGGGTTTCACCATGTTGGCCAGGATGGTC T C AC244669.1 Ensembl:ENSG00000223804 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1434297093 Functional Loss SNV dbSNP153 33..33 33 - - - 11052 RMVar_ID_11052 Human_SNP_ID_30246231 A-to-I Human chr1 + 121596053 121596053 121596053 CATTTTACTTTCTATGAGATTGACTTAACGTTAGATAGCTCAGATAAGTGGCATCATACAGCATT CATTTTACTTTCTATGAGATTGACTTAACGTTCGATAGCTCAGATAAGTGGCATCATACAGCATT A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1235541012 Functional Loss SNV dbSNP153 33..33 33 - - - 11053 RMVar_ID_11053 Human_SNP_ID_402641992 A-to-I Human chr9 - 75008460 75008460 75008460 GGGCGTGGTGGAGTGCACCTGTGATTCCAGCTACTTGGAAGGCTGAGGCAGGAGAATTGCTTGAA GGGCGTGGTGGAGTGCACCTGTGATTCCAGCTGCTTGGAAGGCTGAGGCAGGAGAATTGCTTGAA T C CARNMT1 Ensembl:ENSG00000156017 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs779147448 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_257184,RMVar_hsa_circ_257180,RMVar_hsa_circ_257178,RMVar_hsa_circ_257177,RMVar_hsa_circ_267708,RMVar_hsa_circ_257179,RMVar_hsa_circ_257181,RMVar_hsa_circ_356462,RMVar_hsa_circ_266562,RMVar_hsa_circ_58285,RMVar_hsa_circ_279063,RMVar_hsa_circ_257182,RMVar_hsa_circ_257185,RMVar_hsa_circ_257186 11054 RMVar_ID_11054 Human_SNP_ID_402642829 A-to-I Human chr9 - 75011643 75011643 75011643 AGTCACAGAGCTGGGTGTCAAGGCTCATGTCTATAATCCCAGTACTTTGAGAGACTGAGATGGGA AGTCACAGAGCTGGGTGTCAAGGCTCATGTCTGTAATCCCAGTACTTTGAGAGACTGAGATGGGA T C CARNMT1,AL158825.2 Ensembl:ENSG00000156017,Ensembl:ENSG00000229587 Protein coding,lincRNA intron,intron GSE38233;GSE107867 cultured B-cells;ASD brains,cerebellum - 24183664,30559470 RNA-Seq:(High) rs868353869 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_257184,RMVar_hsa_circ_257180,RMVar_hsa_circ_257178,RMVar_hsa_circ_257177,RMVar_hsa_circ_267708,RMVar_hsa_circ_257179,RMVar_hsa_circ_257181,RMVar_hsa_circ_356462,RMVar_hsa_circ_266562,RMVar_hsa_circ_58285,RMVar_hsa_circ_279063,RMVar_hsa_circ_257182,RMVar_hsa_circ_257185,RMVar_hsa_circ_257186 11055 RMVar_ID_11055 Human_SNP_ID_402643829 A-to-I Human chr9 - 75015693 75015693 75015693 CGACCTCTGCCTCCTGGGTTCAAGTGATTCTCATGCCTCAGACTCCGAAGTAGCTGGGACTGCAG CGACCTCTGCCTCCTGGGTTCAAGTGATTCTCGTGCCTCAGACTCCGAAGTAGCTGGGACTGCAG T C CARNMT1,AL158825.2 Ensembl:ENSG00000156017,Ensembl:ENSG00000229587 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs967274149 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_257184,RMVar_hsa_circ_257180,RMVar_hsa_circ_257178,RMVar_hsa_circ_257177,RMVar_hsa_circ_267708,RMVar_hsa_circ_257179,RMVar_hsa_circ_257181,RMVar_hsa_circ_356462,RMVar_hsa_circ_266562,RMVar_hsa_circ_58285,RMVar_hsa_circ_279063,RMVar_hsa_circ_257182,RMVar_hsa_circ_257185,RMVar_hsa_circ_257186 11056 RMVar_ID_11056 Human_SNP_ID_402645442 A-to-I Human chr9 - 75021892 75021892 75021892 GCTCTGTTACGCAGCCTGTAGTGCAGTGACACAATCATAGCTCGCTGCCCCCTTGACTTTCTGGG GCTCTGTTACGCAGCCTGTAGTGCAGTGACACGATCATAGCTCGCTGCCCCCTTGACTTTCTGGG T C CARNMT1 Ensembl:ENSG00000156017 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs998406467 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58285,RMVar_hsa_circ_48153 11057 RMVar_ID_11057 Human_SNP_ID_402645574 A-to-I Human chr9 - 75022362 75022362 75022362 AAAATTAGCCGGGCATGGTGGTGTGCACCTGTAGTCCCAGCTACTTGGGAGACTGAACCAGAAGA AAAATTAGCCGGGCATGGTGGTGTGCACCTGTCGTCCCAGCTACTTGGGAGACTGAACCAGAAGA T G CARNMT1 Ensembl:ENSG00000156017 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1303135536 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58285,RMVar_hsa_circ_48153 11058 RMVar_ID_11058 Human_SNP_ID_402984131 A-to-I Human chr9 + 76396334 76396334 76396334 AAAATGGGCGGGGCATGGTGGCTTACGCCTGTAATCCCAGCACTCTGGGAGACCGAGGTGAGCGG AAAATGGGCGGGGCATGGTGGCTTACGCCTGTGATCCCAGCACTCTGGGAGACCGAGGTGAGCGG A G lnc-GCNT1-7 RNACentral:URS0000D587DF lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1428527968 Functional Loss SNV dbSNP153 33..33 33 - - - 11059 RMVar_ID_11059 Human_SNP_ID_403065610 A-to-I Human chr9 - 76731476 76731476 76731476 AAAAAAATAAAAAAACAAAATTAGCTGGGTATAGTGGTGTGTGCCTGCAGTCCAGCTACTCAGGA AAAAAAATAAAAAAACAAAATTAGCTGGGTATGGTGGTGTGTGCCTGCAGTCCAGCTACTCAGGA T C PRUNE2 Ensembl:ENSG00000106772 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1202882749 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_257221,RMVar_hsa_circ_120372 11060 RMVar_ID_11060 Human_SNP_ID_403221286 A-to-I Human chr9 + 77348134 77348134 77348134 ACCCAGCAGTCCCCTTCCTGGGTATGTACTCAAAGGAATAGAAATCATTCTCTTATAAAGATAGA ACCCAGCAGTCCCCTTCCTGGGTATGTACTCAGAGGAATAGAAATCATTCTCTTATAAAGATAGA A G VPS13A Ensembl:ENSG00000197969 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1336546165 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3907,RMVar_hsa_circ_366337,RMVar_hsa_circ_28409,RMVar_hsa_circ_60366,RMVar_hsa_circ_340673,RMVar_hsa_circ_95947,RMVar_hsa_circ_85615,RMVar_hsa_circ_257237,RMVar_hsa_circ_257238,RMVar_hsa_circ_127088,RMVar_hsa_circ_257246,RMVar_hsa_circ_52395,RMVar_hsa_circ_257255,RMVar_hsa_circ_341859,RMVar_hsa_circ_354675,RMVar_hsa_circ_356269,RMVar_hsa_circ_23700,RMVar_hsa_circ_275883,RMVar_hsa_circ_257256,RMVar_hsa_circ_290852,RMVar_hsa_circ_360608,RMVar_hsa_circ_320698,RMVar_hsa_circ_290206,RMVar_hsa_circ_257258,RMVar_hsa_circ_71793,RMVar_hsa_circ_257259,RMVar_hsa_circ_353237,RMVar_hsa_circ_72588,RMVar_hsa_circ_59538,RMVar_hsa_circ_303889,RMVar_hsa_circ_257260,RMVar_hsa_circ_31860 11061 RMVar_ID_11061 Human_SNP_ID_403357629 A-to-I Human chr9 - 77870491 77870491 77870491 AAACCCCATCTCTACTAAAAATACAAAAAATTAGCCAGGGCGCCTTGGCAGGCGCCTGTAGTCCC AAACCCCATCTCTACTAAAAATACAAAAAATTTGCCAGGGCGCCTTGGCAGGCGCCTGTAGTCCC T A GNAQ Ensembl:ENSG00000156052 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs545213897 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51040,RMVar_hsa_circ_330530,RMVar_hsa_circ_271109,RMVar_hsa_circ_257280 11062 RMVar_ID_11062 Human_SNP_ID_403358465 A-to-I Human chr9 - 77873977 77873977 77873977 CCTCAGCCTCCCGGGTAGCTGGGATTACAGGCATGCACCACCATGCCTGACTAATTTTGTATTTC CCTCAGCCTCCCGGGTAGCTGGGATTACAGGCCTGCACCACCATGCCTGACTAATTTTGTATTTC T G GNAQ Ensembl:ENSG00000156052 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs912182058 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51040,RMVar_hsa_circ_330530,RMVar_hsa_circ_271109,RMVar_hsa_circ_257280 11063 RMVar_ID_11063 Human_SNP_ID_403358479 A-to-I Human chr9 - 77874022 77874022 77874022 CAGCTCACTGCAACCTCTACCTCCCAGGTTCAAGTGATTCTCCTACCTCAGCCTCCCGGGTAGCT CAGCTCACTGCAACCTCTACCTCCCAGGTTCAGGTGATTCTCCTACCTCAGCCTCCCGGGTAGCT T C GNAQ Ensembl:ENSG00000156052 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs758109160 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51040,RMVar_hsa_circ_330530,RMVar_hsa_circ_271109,RMVar_hsa_circ_257280 11064 RMVar_ID_11064 Human_SNP_ID_403358732 A-to-I Human chr9 - 77874801 77874801 77874801 GCCTGTCCAACATGGCGAAACCTCTACTAAAAATTCAAAAAATTAGTCAAGCATGGTGGCACACA GCCTGTCCAACATGGCGAAACCTCTACTAAAAGTTCAAAAAATTAGTCAAGCATGGTGGCACACA T C GNAQ Ensembl:ENSG00000156052 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1256003589 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51040,RMVar_hsa_circ_330530,RMVar_hsa_circ_271109,RMVar_hsa_circ_257280 11065 RMVar_ID_11065 Human_SNP_ID_403360019 A-to-I Human chr9 - 77880449 77880449 77880449 TTGATCCCAGGAGTTCAAGGCTAAAGTGAGCTAGGATCACAACACTGCACTCCAGCCTTCCAGTT TTGATCCCAGGAGTTCAAGGCTAAAGTGAGCTGGGATCACAACACTGCACTCCAGCCTTCCAGTT T C GNAQ Ensembl:ENSG00000156052 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1175039104 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16701779 RMVar_hsa_circ_51040,RMVar_hsa_circ_330530,RMVar_hsa_circ_271109,RMVar_hsa_circ_257280 11066 RMVar_ID_11066 Human_SNP_ID_403361663 A-to-I Human chr9 - 77887014 77887014 77887014 AGGTTCAAGAGATTCTCCTGCCTTAGCCTCCAAAGTAACTGGGACCACAGGCACCCGCCACCACG AGGTTCAAGAGATTCTCCTGCCTTAGCCTCCAGAGTAACTGGGACCACAGGCACCCGCCACCACG T C GNAQ Ensembl:ENSG00000156052 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1280825999 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51040,RMVar_hsa_circ_330530,RMVar_hsa_circ_271109,RMVar_hsa_circ_257280 11067 RMVar_ID_11067 Human_SNP_ID_403369622 A-to-I Human chr9 - 77918974 77918974 77918974 TGGAGGTTGCAGTGAGCTGAGATCATGCCGCTACGCTGCAGCCTGGGCAACAGAGCAAGACTCCA TGGAGGTTGCAGTGAGCTGAGATCATGCCGCTGCGCTGCAGCCTGGGCAACAGAGCAAGACTCCA T C GNAQ Ensembl:ENSG00000156052 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs919155670 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26243873 RMVar_hsa_circ_51040,RMVar_hsa_circ_330530,RMVar_hsa_circ_271109,RMVar_hsa_circ_257280 11068 RMVar_ID_11068 Human_SNP_ID_403379016 A-to-I Human chr9 - 77957193 77957193 77957193 CACCACCACACCTGGCTAATTTTTTTATTTTTAGTAGAGAAGGGGTTTCACTATGTTGGCCAGAC CACCACCACACCTGGCTAATTTTTTTATTTTTGGTAGAGAAGGGGTTTCACTATGTTGGCCAGAC T C GNAQ Ensembl:ENSG00000156052 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1353254465 Functional Loss SNV dbSNP153 33..33 33 - - - 11069 RMVar_ID_11069 Human_SNP_ID_403457394 A-to-I Human chr9 + 78272047 78272047 78272047 TGAAGTGATCTTCCTGCCTCAGCCCCCCTAGTAACTGGGATTACAGGCACACACCACCATGCCTG TGAAGTGATCTTCCTGCCTCAGCCCCCCTAGTCACTGGGATTACAGGCACACACCACCATGCCTG A C CEP78 Ensembl:ENSG00000148019 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs191478798 Functional Loss SNV dbSNP153 33..33 33 - - - 11070 RMVar_ID_11070 Human_SNP_ID_403457431 A-to-I Human chr9 + 78272192 78272192 78272192 CACCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGCATCCGGCCAAGATGG CACCCACCTCGGCCTCCCAAAGTGCTGGGATTGCAGGCATGAGCCACTGCATCCGGCCAAGATGG A G CEP78 Ensembl:ENSG00000148019 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs933768354 Functional Loss SNV dbSNP153 33..33 33 - - - 11071 RMVar_ID_11071 Human_SNP_ID_403457433 A-to-I Human chr9 + 78272198 78272198 78272198 CCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGCATCCGGCCAAGATGGGTTCTT CCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCATCCGGCCAAGATGGGTTCTT A G CEP78 Ensembl:ENSG00000148019 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1003455851 Functional Loss SNV dbSNP153 33..33 33 - - - 11072 RMVar_ID_11072 Human_SNP_ID_403457456 A-to-I Human chr9 + 78272287 78272275 78272288 GCCTCAAATGATCCTCCCACCTTGGCCTCCCAAAGTGCTGAGACTACAGACCTGAGCCACTGTGC GCCTCAAATGATCCTCCCACC_____________GTGCTGAGACTACAGACCTGAGCCACTGTGC CTTGGCCTCCCAAA C CEP78 Ensembl:ENSG00000148019 Protein coding 3'UTR GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1215523678 Functional Loss DEL dbSNP153 22..34 33 - - - Human_RBP_ID_16703435 11073 RMVar_ID_11073 Human_SNP_ID_403457460 A-to-I Human chr9 + 78272286 78272286 78272286 GGCCTCAAATGATCCTCCCACCTTGGCCTCCCAAAGTGCTGAGACTACAGACCTGAGCCACTGTG GGCCTCAAATGATCCTCCCACCTTGGCCTCCCGAAGTGCTGAGACTACAGACCTGAGCCACTGTG A G CEP78 Ensembl:ENSG00000148019 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956855604 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16703435 11074 RMVar_ID_11074 Human_SNP_ID_403457464 A-to-I Human chr9 + 78272300 78272300 78272300 CTCCCACCTTGGCCTCCCAAAGTGCTGAGACTACAGACCTGAGCCACTGTGCCCAGCCCCATGAA CTCCCACCTTGGCCTCCCAAAGTGCTGAGACTGCAGACCTGAGCCACTGTGCCCAGCCCCATGAA A G CEP78 Ensembl:ENSG00000148019 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs944267513 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16703435 11075 RMVar_ID_11075 Human_SNP_ID_403457795 A-to-I Human chr9 + 78273600 78273600 78273600 TACTAAAAATACAAAAAAAAAAAAAAAAAATTAGCTGGGTGTCATGGCGCATGCCTGTAATCCCA TACTAAAAATACAAAAAAAAAAAAAAAAAATTGGCTGGGTGTCATGGCGCATGCCTGTAATCCCA A G CEP78 Ensembl:ENSG00000148019 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335143774 Functional Loss SNV dbSNP153 33..33 33 - - - 11076 RMVar_ID_11076 Human_SNP_ID_403457810 A-to-I Human chr9 + 78273636 78273636 78273636 GGGTGTCATGGCGCATGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAA GGGTGTCATGGCGCATGCCTGTAATCCCAGCTGCTCGGGAGGCTGAGGCAGGAGAATCGCTTGAA A G CEP78 Ensembl:ENSG00000148019 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs968684507 Functional Loss SNV dbSNP153 33..33 33 - - - 11077 RMVar_ID_11077 Human_SNP_ID_403458328 A-to-I Human chr9 + 78275800 78275800 78275800 AAAACAAAACAAAACAAAAAAACCCAAAACTTAGCCAGGCATGGTGGTGCGTGCATGTAGTCCCA AAAACAAAACAAAACAAAAAAACCCAAAACTTTGCCAGGCATGGTGGTGCGTGCATGTAGTCCCA A T CEP78 Ensembl:ENSG00000148019 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs889382192 Functional Loss SNV dbSNP153 33..33 33 - - - 11078 RMVar_ID_11078 Human_SNP_ID_404803810 A-to-I Human chr9 - 83654530 83654530 83654530 TGGTAATTCCATTGTTAACTTTTTGTGGAACTACTGAATGGTTTCCATAGTGGCTGCACCATTTT TGGTAATTCCATTGTTAACTTTTTGTGGAACTGCTGAATGGTTTCCATAGTGGCTGCACCATTTT T C RF00017-4706 RNACentral:URS000095B12E SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs554869684 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16717855 11079 RMVar_ID_11079 Human_SNP_ID_404808928 A-to-I Human chr9 - 83673832 83673832 83673832 GCATCACCGCACTCCAGCCTGGGAGACAGAGCAAGACCCTGTCTCAAAACAAAACAAATAACAGT GCATCACCGCACTCCAGCCTGGGAGACAGAGCGAGACCCTGTCTCAAAACAAAACAAATAACAGT T C UBQLN1 Ensembl:ENSG00000135018 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1262912995 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_257412,RMVar_hsa_circ_64274,RMVar_hsa_circ_257402,RMVar_hsa_circ_257398,RMVar_hsa_circ_106466,RMVar_hsa_circ_82923,RMVar_hsa_circ_84247,RMVar_hsa_circ_78767,RMVar_hsa_circ_257400,RMVar_hsa_circ_257401,RMVar_hsa_circ_257399,RMVar_hsa_circ_335685,RMVar_hsa_circ_278466,RMVar_hsa_circ_14758,RMVar_hsa_circ_257410,RMVar_hsa_circ_257408,RMVar_hsa_circ_281760,RMVar_hsa_circ_275132,RMVar_hsa_circ_99008,RMVar_hsa_circ_257409,RMVar_hsa_circ_62064,RMVar_hsa_circ_285962,RMVar_hsa_circ_374410,RMVar_hsa_circ_257411,RMVar_hsa_circ_373398,RMVar_hsa_circ_257414,RMVar_hsa_circ_257413 11080 RMVar_ID_11080 Human_SNP_ID_404811987 A-to-I Human chr9 - 83684703 83684703 83684703 GGGTTCAAGCGATTCTCCCGCCTCAGCCTCCCAAGTAGCTGGAATTACAGGCATGCGCCACCACG GGGTTCAAGCGATTCTCCCGCCTCAGCCTCCCTAGTAGCTGGAATTACAGGCATGCGCCACCACG T A UBQLN1 Ensembl:ENSG00000135018 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1422937948 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_257412,RMVar_hsa_circ_64274,RMVar_hsa_circ_257398,RMVar_hsa_circ_78767,RMVar_hsa_circ_257399,RMVar_hsa_circ_285962,RMVar_hsa_circ_257425,RMVar_hsa_circ_257420,RMVar_hsa_circ_276748,RMVar_hsa_circ_257423,RMVar_hsa_circ_274895,RMVar_hsa_circ_257424,RMVar_hsa_circ_289054,RMVar_hsa_circ_257429,RMVar_hsa_circ_270688 11081 RMVar_ID_11081 Human_SNP_ID_404812006 A-to-I Human chr9 - 83684771 83684764 83684772 AATTTCACTCTTGTTGCCCAGGCTGGAGTGCAACGGTGCGATCTCAGCTCACTGCAACGTCTGCC AATTTCACTCTTGTTGCCCAGGCTGGAGTGC________GATCTCAGCTCACTGCAACGTCTGCC CGCACCGTT C UBQLN1 Ensembl:ENSG00000135018 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1185775313 Functional Loss DEL dbSNP153 32..39 33 - - - RMVar_hsa_circ_257412,RMVar_hsa_circ_64274,RMVar_hsa_circ_257398,RMVar_hsa_circ_78767,RMVar_hsa_circ_257399,RMVar_hsa_circ_285962,RMVar_hsa_circ_257425,RMVar_hsa_circ_257420,RMVar_hsa_circ_276748,RMVar_hsa_circ_257423,RMVar_hsa_circ_274895,RMVar_hsa_circ_257424,RMVar_hsa_circ_289054,RMVar_hsa_circ_257429,RMVar_hsa_circ_270688 11082 RMVar_ID_11082 Human_SNP_ID_404812012 A-to-I Human chr9 - 83684771 83684771 83684771 AATTTCACTCTTGTTGCCCAGGCTGGAGTGCAACGGTGCGATCTCAGCTCACTGCAACGTCTGCC AATTTCACTCTTGTTGCCCAGGCTGGAGTGCAGCGGTGCGATCTCAGCTCACTGCAACGTCTGCC T C UBQLN1 Ensembl:ENSG00000135018 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1203488696 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_257412,RMVar_hsa_circ_64274,RMVar_hsa_circ_257398,RMVar_hsa_circ_78767,RMVar_hsa_circ_257399,RMVar_hsa_circ_285962,RMVar_hsa_circ_257425,RMVar_hsa_circ_257420,RMVar_hsa_circ_276748,RMVar_hsa_circ_257423,RMVar_hsa_circ_274895,RMVar_hsa_circ_257424,RMVar_hsa_circ_289054,RMVar_hsa_circ_257429,RMVar_hsa_circ_270688 11083 RMVar_ID_11083 Human_SNP_ID_404815087 A-to-I Human chr9 - 83697071 83697071 83697071 GCTTTTCAGTCTTTAAAGTTCATTGAATAGCTAGGTGTGGTGGTGCAAGCCTGTAGTCCCAGCTA GCTTTTCAGTCTTTAAAGTTCATTGAATAGCTCGGTGTGGTGGTGCAAGCCTGTAGTCCCAGCTA T G UBQLN1 Ensembl:ENSG00000135018 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417555814 Functional Loss SNV dbSNP153 33..33 33 - - - 11084 RMVar_ID_11084 Human_SNP_ID_404817024 A-to-I Human chr9 - 83704763 83704763 83704763 GGAGTGCAATGGCATGGTGTCGGCTCACTGCAACCTCCCCTTCCCGGGTTCAAGGATTCTCCCAC GGAGTGCAATGGCATGGTGTCGGCTCACTGCAGCCTCCCCTTCCCGGGTTCAAGGATTCTCCCAC T C UBQLN1 Ensembl:ENSG00000135018 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1322417969 Functional Loss SNV dbSNP153 33..33 33 - - - 11085 RMVar_ID_11085 Human_SNP_ID_404843960 A-to-I Human chr9 - 83808348 83808348 83808348 CCAGTGACCTGCCCACCTCGGCCTCCCAAAGTACTGGGATTACAGGTGTGAGCCACTGCACCCGG CCAGTGACCTGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACTGCACCCGG T C GKAP1 Ensembl:ENSG00000165113 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1226721868 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59099 11086 RMVar_ID_11086 Human_SNP_ID_404867301 A-to-I Human chr9 - 83904485 83904485 83904485 GCATGCCTGTAATCCCAACTACTCGGGAGGCTAAGGCAGGAGAATCACTTGAACCCGAGGTAGAG GCATGCCTGTAATCCCAACTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCCGAGGTAGAG T C KIF27 Ensembl:ENSG00000165115 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs754606930 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25217,RMVar_hsa_circ_48951,RMVar_hsa_circ_257442,RMVar_hsa_circ_115085,RMVar_hsa_circ_302651,RMVar_hsa_circ_360258,RMVar_hsa_circ_360083,RMVar_hsa_circ_67728,RMVar_hsa_circ_322153,RMVar_hsa_circ_269135,RMVar_hsa_circ_334972,RMVar_hsa_circ_302729,RMVar_hsa_circ_313718 11087 RMVar_ID_11087 Human_SNP_ID_404880004 A-to-I Human chr9 - 83952230 83952230 83952230 CCCATAATCCCAACACATTGGGTGGCTGAGGTAAGAGGATTGCTTGAGCCCAGGAGGTCGAGACC CCCATAATCCCAACACATTGGGTGGCTGAGGTGAGAGGATTGCTTGAGCCCAGGAGGTCGAGACC T C C9orf64 Ensembl:ENSG00000165118 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs776572680 Functional Loss SNV dbSNP153 33..33 33 - - - 11088 RMVar_ID_11088 Human_SNP_ID_404885957 A-to-I Human chr9 - 83971931 83971931 83971931 CCCCTCCTCCCGGACGAGGCGGCCGGGGTGGTAGCAGAGCTCGGAATCTTCCTCTTCCTCCACCA CCCCTCCTCCCGGACGAGGCGGCCGGGGTGGTGGCAGAGCTCGGAATCTTCCTCTTCCTCCACCA T C HNRNPK Ensembl:ENSG00000165119 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1329106171 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_256197,Human_RBP_ID_721102,Human_RBP_ID_1059762,Human_RBP_ID_5043581,Human_RBP_ID_7958336,Human_RBP_ID_9315109,Human_RBP_ID_16719655,Human_RBP_ID_18138578,Human_RBP_ID_22466132,Human_RBP_ID_22838867,Human_RBP_ID_24309935,Human_RBP_ID_26244056,Human_RBP_ID_27138362,Human_RBP_ID_27376356 Human_Splice_Rec_1056875,Human_Splice_Rec_1056907,Human_Splice_Rec_1056937,Human_Splice_Rec_1056969,Human_Splice_Rec_1057013 Human_miRNA_ID_2395193,Human_miRNA_ID_2395194 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 11089 RMVar_ID_11089 Human_SNP_ID_404892684 A-to-I Human chr9 + 83994211 83994211 83994211 TACATATTCTGGGTAATAACACCTTATCTGATATGTGGTTTGCAAATATTTTCTCCCATTCCATA TACATATTCTGGGTAATAACACCTTATCTGATGTGTGGTTTGCAAATATTTTCTCCCATTCCATA A G RMI1 Ensembl:ENSG00000178966 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1251473107 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18910761 11090 RMVar_ID_11090 Human_SNP_ID_404965914 A-to-I Human chr9 - 84304850 84304850 84304850 ACCCGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACTGTGTTGGCCGGGCTGGTCTCGA ACCCGGCTAATTTTTGTATTTTTAGTAGAGACTGGGTTTCACTGTGTTGGCCGGGCTGGTCTCGA T A SLC28A3 Ensembl:ENSG00000197506 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569899606 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_185531 11091 RMVar_ID_11091 Human_SNP_ID_404965915 A-to-I Human chr9 - 84304850 84304850 84304850 ACCCGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACTGTGTTGGCCGGGCTGGTCTCGA ACCCGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACTGTGTTGGCCGGGCTGGTCTCGA T C SLC28A3 Ensembl:ENSG00000197506 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569899606 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_185531 11092 RMVar_ID_11092 Human_SNP_ID_405062615 A-to-I Human chr9 + 84687403 84687403 84687403 CTCATTAGACCTATTTTTGTTTGTTGGAGATCAGGTAACCCTGGAGTGATTATTTTCCCCTGGAT CTCATTAGACCTATTTTTGTTTGTTGGAGATCGGGTAACCCTGGAGTGATTATTTTCCCCTGGAT A G NTRK2 Ensembl:ENSG00000148053 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs867672743 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_52644,RMVar_hsa_circ_117460,RMVar_hsa_circ_113967,RMVar_hsa_circ_257462,RMVar_hsa_circ_257463 11093 RMVar_ID_11093 Human_SNP_ID_405062616 A-to-I Human chr9 + 84687407 84687407 84687407 TTAGACCTATTTTTGTTTGTTGGAGATCAGGTAACCCTGGAGTGATTATTTTCCCCTGGATTTTC TTAGACCTATTTTTGTTTGTTGGAGATCAGGTGACCCTGGAGTGATTATTTTCCCCTGGATTTTC A G NTRK2 Ensembl:ENSG00000148053 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1053706178 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_52644,RMVar_hsa_circ_117460,RMVar_hsa_circ_113967,RMVar_hsa_circ_257462,RMVar_hsa_circ_257463 11094 RMVar_ID_11094 Human_SNP_ID_405089741 A-to-I Human chr9 + 84803434 84803434 84803434 CACATCTGCCTGCAGCAGCGTCAGAAGCAGATATGCGGCCCTACCTTGGTCTGGGAGCAGGAGCT CACATCTGCCTGCAGCAGCGTCAGAAGCAGATGTGCGGCCCTACCTTGGTCTGGGAGCAGGAGCT A G NTRK2 Ensembl:ENSG00000148053 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs983539658 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269482,RMVar_hsa_circ_24099,RMVar_hsa_circ_40793,RMVar_hsa_circ_8285,RMVar_hsa_circ_297444,RMVar_hsa_circ_319769 11095 RMVar_ID_11095 Human_SNP_ID_405265709 A-to-I Human chr9 - 85543995 85543995 85543995 GAGGTGAGGAGTTCAAGATCAGCATGGCCAACATGGTGAAACTCCACCTCCACGAAAAATACAAA GAGGTGAGGAGTTCAAGATCAGCATGGCCAACGTGGTGAAACTCCACCTCCACGAAAAATACAAA T C - - Other Unknown GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 29129909,30559470 RNA-Seq:(High) rs1254051797 Functional Loss SNV dbSNP153 33..33 33 - - - 11096 RMVar_ID_11096 Human_SNP_ID_405265725 A-to-I Human chr9 - 85544066 85544066 85544066 TTTAGGGCTGGGTGCAGAGGCTCATGCCTGTAATCCCAGCACTCTGAGAGGCCGAGGCGGGTGGA TTTAGGGCTGGGTGCAGAGGCTCATGCCTGTAGTCCCAGCACTCTGAGAGGCCGAGGCGGGTGGA T C - - Other Unknown GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1318722495 Functional Loss SNV dbSNP153 33..33 33 - - - 11097 RMVar_ID_11097 Human_SNP_ID_405266253 A-to-I Human chr9 - 85546330 85546330 85546330 CACTTGAGGTCAGGAGTTTGAGCCTGGTCAACATGGTGAAACCCTGTCTCTACTAAAAATACAAA CACTTGAGGTCAGGAGTTTGAGCCTGGTCAACTTGGTGAAACCCTGTCTCTACTAAAAATACAAA T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1352744321 Functional Loss SNV dbSNP153 33..33 33 - - - 11098 RMVar_ID_11098 Human_SNP_ID_405297027 A-to-I Human chr9 - 85679546 85679546 85679546 AAAATTAGTTGGATGTGGTGGCGGACGCCTGTAGTCCCAGCTGCTTGGGAGGCTGAGGCAGGAGA AAAATTAGTTGGATGTGGTGGCGGACGCCTGTCGTCCCAGCTGCTTGGGAGGCTGAGGCAGGAGA T G AGTPBP1 Ensembl:ENSG00000135049 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1399970344 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_350274,RMVar_hsa_circ_22976,RMVar_hsa_circ_41581,RMVar_hsa_circ_305251,RMVar_hsa_circ_257537,RMVar_hsa_circ_257544,RMVar_hsa_circ_15670,RMVar_hsa_circ_337582,RMVar_hsa_circ_299158,RMVar_hsa_circ_312457,RMVar_hsa_circ_257542,RMVar_hsa_circ_257543,RMVar_hsa_circ_367930,RMVar_hsa_circ_334037,RMVar_hsa_circ_271527,RMVar_hsa_circ_257551,RMVar_hsa_circ_257550,RMVar_hsa_circ_305757,RMVar_hsa_circ_268680,RMVar_hsa_circ_257563,RMVar_hsa_circ_284296,RMVar_hsa_circ_305984,RMVar_hsa_circ_270553,RMVar_hsa_circ_257561,RMVar_hsa_circ_257562,RMVar_hsa_circ_257568,RMVar_hsa_circ_257565,RMVar_hsa_circ_281299,RMVar_hsa_circ_305576,RMVar_hsa_circ_276464,RMVar_hsa_circ_323866,RMVar_hsa_circ_257564,RMVar_hsa_circ_297967,RMVar_hsa_circ_257569,RMVar_hsa_circ_257567 11099 RMVar_ID_11099 Human_SNP_ID_405307897 A-to-I Human chr9 - 85724162 85724162 85724162 CTGCCTCAGCCTCCTGAGTAGCTTGGATTACAAGTACTCACCACCACACCCGGCTAATTTTTGTA CTGCCTCAGCCTCCTGAGTAGCTTGGATTACAGGTACTCACCACCACACCCGGCTAATTTTTGTA T C AGTPBP1 Ensembl:ENSG00000135049 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1337400040 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16721894 11100 RMVar_ID_11100 Human_SNP_ID_405308278 A-to-I Human chr9 - 85725713 85725713 85725713 CAGAAATGGGGTCTCCCTATATTGTGCAGGCTAGTCTCGAACTCTTGGGCTCAAGCAGTTCTCCC CAGAAATGGGGTCTCCCTATATTGTGCAGGCTGGTCTCGAACTCTTGGGCTCAAGCAGTTCTCCC T C AGTPBP1 Ensembl:ENSG00000135049 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs974142218 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16721954 11101 RMVar_ID_11101 Human_SNP_ID_405328257 A-to-I Human chr9 + 85810648 85810648 85810648 ACGTGCCTGTAGTCCCAGGTACTCCGGAGGCCAAGGTGGGAGAATCACCTGAGACCAGGAAGTTG ACGTGCCTGTAGTCCCAGGTACTCCGGAGGCCGAGGTGGGAGAATCACCTGAGACCAGGAAGTTG A G AL353743.1 Ensembl:ENSG00000165121 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1387599686 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67785 11102 RMVar_ID_11102 Human_SNP_ID_405336335 A-to-I Human chr9 + 85843980 85843980 85843980 GTCTCACTGAAGACTTCTCTTGAATAGCAGCTACTTCTGCCAACTAATAATTACAGGACATCTAT GTCTCACTGAAGACTTCTCTTGAATAGCAGCTCCTTCTGCCAACTAATAATTACAGGACATCTAT A C AL353743.1 Ensembl:ENSG00000165121 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459470614 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17438538,Human_RBP_ID_18521343 RMVar_hsa_circ_306578 11103 RMVar_ID_11103 Human_SNP_ID_405336336 A-to-I Human chr9 + 85843980 85843980 85843980 GTCTCACTGAAGACTTCTCTTGAATAGCAGCTACTTCTGCCAACTAATAATTACAGGACATCTAT GTCTCACTGAAGACTTCTCTTGAATAGCAGCTGCTTCTGCCAACTAATAATTACAGGACATCTAT A G AL353743.1 Ensembl:ENSG00000165121 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459470614 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17438538,Human_RBP_ID_18521343 RMVar_hsa_circ_306578 11104 RMVar_ID_11104 Human_SNP_ID_405342331 A-to-I Human chr9 + 85867432 85867432 85867432 GGAAAGCAGTTTGGAGATTTGTGAAAGAACTTAGAACAGAAATACCATTAGGCCCAGCAATCCCG GGAAAGCAGTTTGGAGATTTGTGAAAGAACTTTGAACAGAAATACCATTAGGCCCAGCAATCCCG A T lnc-NAA35-6,lnc-NAA35-1 RNACentral:URS00008B9052,RNACentral:URS00008B32CA lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs527454742 Functional Loss SNV dbSNP153 33..33 33 - - - 11105 RMVar_ID_11105 Human_SNP_ID_405347883 A-to-I Human chr9 + 85888604 85888604 85888604 CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGACGCATGCCACCACGCCTGGCTAATTGTT CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTGCAGACGCATGCCACCACGCCTGGCTAATTGTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941417187 Functional Loss SNV dbSNP153 33..33 33 - - - 11106 RMVar_ID_11106 Human_SNP_ID_405366536 A-to-I Human chr9 + 85966161 85966160 85966161 CTGGGTTTTGCTTTGTTTGCCAGGCTGGTCTCAAACTGCAATGCTCAAGTGATCTTCCCACCCCA CTGGGTTTTGCTTTGTTTGCCAGGCTGGTCTC_AACTGCAATGCTCAAGTGATCTTCCCACCCCA CA C NAA35 Ensembl:ENSG00000135040 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1318275184 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_22966,RMVar_hsa_circ_56890,RMVar_hsa_circ_45058,RMVar_hsa_circ_62088,RMVar_hsa_circ_15804,RMVar_hsa_circ_294618,RMVar_hsa_circ_257576,RMVar_hsa_circ_291202,RMVar_hsa_circ_300179,RMVar_hsa_circ_337190,RMVar_hsa_circ_257579,RMVar_hsa_circ_257580,RMVar_hsa_circ_343785,RMVar_hsa_circ_352616,RMVar_hsa_circ_341035,RMVar_hsa_circ_316179,RMVar_hsa_circ_333540,RMVar_hsa_circ_312369,RMVar_hsa_circ_54068,RMVar_hsa_circ_99046,RMVar_hsa_circ_28229,RMVar_hsa_circ_257583,RMVar_hsa_circ_257585,RMVar_hsa_circ_257587,RMVar_hsa_circ_257588,RMVar_hsa_circ_257589,RMVar_hsa_circ_257586,RMVar_hsa_circ_257584,RMVar_hsa_circ_257581,RMVar_hsa_circ_257582 11107 RMVar_ID_11107 Human_SNP_ID_405376952 A-to-I Human chr9 + 86010141 86010141 86010141 ATGGTGGCGCACGCCTGTAGTGCCAGCTACTCAGGAGCCTGAGGTGGGAAAATCGCTTGAACCCA ATGGTGGCGCACGCCTGTAGTGCCAGCTACTCGGGAGCCTGAGGTGGGAAAATCGCTTGAACCCA A G NAA35 Ensembl:ENSG00000135040 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1008866211 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8707370 RMVar_hsa_circ_56890,RMVar_hsa_circ_300179,RMVar_hsa_circ_343785,RMVar_hsa_circ_341035,RMVar_hsa_circ_28229,RMVar_hsa_circ_30293,RMVar_hsa_circ_257583,RMVar_hsa_circ_257581,RMVar_hsa_circ_257582,RMVar_hsa_circ_17672,RMVar_hsa_circ_348508,RMVar_hsa_circ_318528,RMVar_hsa_circ_257594,RMVar_hsa_circ_276889,RMVar_hsa_circ_257596 11108 RMVar_ID_11108 Human_SNP_ID_405381207 A-to-I Human chr9 - 86026943 86026943 86026943 AGGGCAAGTTTGTTGTGGACAGATCTGTGCCTACTTTATTACTGGAGTAAAAGAAAACAAAGTTC AGGGCAAGTTTGTTGTGGACAGATCTGTGCCTGCTTTATTACTGGAGTAAAAGAAAACAAAGTTC T C GOLM1 Ensembl:ENSG00000135052 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1257233772 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_721294,Human_RBP_ID_2066238,Human_RBP_ID_9238661,Human_RBP_ID_17322583,Human_RBP_ID_17436780,Human_RBP_ID_17550344,Human_RBP_ID_18399941,Human_RBP_ID_22411806,Human_RBP_ID_24311065,Human_RBP_ID_27787361 Human_miRNA_ID_299329 11109 RMVar_ID_11109 Human_SNP_ID_405442122 A-to-I Human chr9 - 86267139 86267139 86267139 TTCACTGTAGCCTCTGTCTCCCGGGCTCAAGCAGTCCTCCCACCTCAGCCTCCCGAGTAGCTGGG TTCACTGTAGCCTCTGTCTCCCGGGCTCAAGCTGTCCTCCCACCTCAGCCTCCCGAGTAGCTGGG T A ISCA1 Ensembl:ENSG00000135070 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934354584 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103750,RMVar_hsa_circ_257609 11110 RMVar_ID_11110 Human_SNP_ID_405468168 A-to-I Human chr9 - 86375265 86375265 86375265 GAATCCTCAAACTTTTCAATCTCTCTAAAGAAAATGATGTCCACCAGTATGTTGTAAGAAAGCCC GAATCCTCAAACTTTTCAATCTCTCTAAAGAAGATGATGTCCACCAGTATGTTGTAAGAAAGCCC T C AL353678.1 Ensembl:ENSG00000214908 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879012957 Functional Loss SNV dbSNP153 33..33 33 - - - 11111 RMVar_ID_11111 Human_SNP_ID_405624078 A-to-I Human chr9 + 87004402 87004402 87004402 CAGATGACCATTGTTCTAGAAATTTGAAAGATAAAGAACTAGACTATGAGAAGGCAGGGTGATCA CAGATGACCATTGTTCTAGAAATTTGAAAGATGAAGAACTAGACTATGAGAAGGCAGGGTGATCA A G GAS1RR,GAS1RR:2 RNACentral:URS0000D5D630,RNACentral:URS0000D56EA0 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947496113 Functional Loss SNV dbSNP153 33..33 33 - - - 11112 RMVar_ID_11112 Human_SNP_ID_405750911 A-to-I Human chr9 + 87525501 87525501 87525501 GGACTAAATGATCTTCCTTCAAAGGATTATCCAAGGCATATACTCAATGAAAAACCATGATAGTT GGACTAAATGATCTTCCTTCAAAGGATTATCCGAGGCATATACTCAATGAAAAACCATGATAGTT A G DAPK1 Ensembl:ENSG00000196730 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs556188722 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18911084 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 11113 RMVar_ID_11113 Human_SNP_ID_405759458 A-to-I Human chr9 + 87560196 87560196 87560196 TATTTTTTTTTTAGTAGAGACGGGGTTTCGCCATGTTGACCAGGGTGGTCTAGAATTCCTGACCT TATTTTTTTTTTAGTAGAGACGGGGTTTCGCCGTGTTGACCAGGGTGGTCTAGAATTCCTGACCT A G DAPK1 Ensembl:ENSG00000196730 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs916162341 Functional Loss SNV dbSNP153 33..33 33 - - - 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 11114 RMVar_ID_11114 Human_SNP_ID_405868431 A-to-I Human chr9 - 87966145 87966145 87966145 GACCTCGTGATCTGCCTGCCCGGGCCTCTCAAAGTGCTGGGATTGTAGGCGTGAGCCACCATGCC GACCTCGTGATCTGCCTGCCCGGGCCTCTCAAGGTGCTGGGATTGTAGGCGTGAGCCACCATGCC T C RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1472713107 Functional Loss SNV dbSNP153 33..33 33 - - - 11115 RMVar_ID_11115 Human_SNP_ID_405932890 A-to-I Human chr9 + 88189415 88189415 88189415 AAGAAATGCAAGCATCTTTCCATGTGCTGTCTACATACATCTTCCATATATTCTGGCTCTGATGA AAGAAATGCAAGCATCTTTCCATGTGCTGTCTGCATACATCTTCCATATATTCTGGCTCTGATGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893465317 Functional Loss SNV dbSNP153 33..33 33 - - - 11116 RMVar_ID_11116 Human_SNP_ID_405984688 A-to-I Human chr9 - 88386885 88386885 88386885 AAAAATATTTTTAGTAGAGACGGGGTTTCGCCATGTTGGCCAGGCCGGTCTCAAACTCCTGGCCT AAAAATATTTTTAGTAGAGACGGGGTTTCGCCGTGTTGGCCAGGCCGGTCTCAAACTCCTGGCCT T C AL353748.3 Ensembl:ENSG00000287769 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1315579062 Functional Loss SNV dbSNP153 33..33 33 - - - 11117 RMVar_ID_11117 Human_SNP_ID_405987086 A-to-I Human chr9 + 88393541 88393541 88393541 CAGTGGCGCAGTCTCAGCTGACTGCACCCTCCACCTCCCGGGAGTCAAGCGATTCTCCTGCCTCA CAGTGGCGCAGTCTCAGCTGACTGCACCCTCCGCCTCCCGGGAGTCAAGCGATTCTCCTGCCTCA A G SPIN1 Ensembl:ENSG00000106723 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569587930 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7943940,Human_RBP_ID_16726218 RMVar_hsa_circ_109926,RMVar_hsa_circ_91298,RMVar_hsa_circ_257656,RMVar_hsa_circ_257657 11118 RMVar_ID_11118 Human_SNP_ID_405987610 A-to-I Human chr9 + 88395069 88395069 88395069 TGACCTCGTGATCTGTCCGCCTCGGCCTGCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGC TGACCTCGTGATCTGTCCGCCTCGGCCTGCCATAGTGCTGGGATTACAGGCGTGAGCCACCGCGC A T SPIN1 Ensembl:ENSG00000106723 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs943695231 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109926,RMVar_hsa_circ_91298,RMVar_hsa_circ_257656,RMVar_hsa_circ_257658,RMVar_hsa_circ_257657 11119 RMVar_ID_11119 Human_SNP_ID_405988441 A-to-I Human chr9 + 88397813 88397813 88397813 CTGGCTAATTTTTTTGTATTTTTAGTAGAGACAGGGTTTCACCTTGTTGGCCAGACTGGTCGCCA CTGGCTAATTTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCTTGTTGGCCAGACTGGTCGCCA A G SPIN1 Ensembl:ENSG00000106723 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1410169774 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109926,RMVar_hsa_circ_91298,RMVar_hsa_circ_257656,RMVar_hsa_circ_257657 11120 RMVar_ID_11120 Human_SNP_ID_405988494 A-to-I Human chr9 + 88397983 88397983 88397983 CACTCCAGTTGCCTAGGCTGTAGTGCAGTGGCACAGTTTTGGCTCATTGCAGCCTCGACCTTCCC CACTCCAGTTGCCTAGGCTGTAGTGCAGTGGCGCAGTTTTGGCTCATTGCAGCCTCGACCTTCCC A G SPIN1 Ensembl:ENSG00000106723 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs890182830 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16726341 RMVar_hsa_circ_109926,RMVar_hsa_circ_91298,RMVar_hsa_circ_257656,RMVar_hsa_circ_257657 11121 RMVar_ID_11121 Human_SNP_ID_405988697 A-to-I Human chr9 + 88398679 88398679 88398679 CTCATCGCAACCTCCGCCTCGTGGGATCAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGG CTCATCGCAACCTCCGCCTCGTGGGATCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGG A G SPIN1 Ensembl:ENSG00000106723 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1296569651 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109926,RMVar_hsa_circ_91298,RMVar_hsa_circ_257656,RMVar_hsa_circ_257657 11122 RMVar_ID_11122 Human_SNP_ID_405988729 A-to-I Human chr9 + 88398803 88398803 88398803 TCCATGTTGGTCAGGCTGGTCTTGAACTCCCCACCTCAGGTCATCCGCCTGCCTTGGCCTCCCTG TCCATGTTGGTCAGGCTGGTCTTGAACTCCCCGCCTCAGGTCATCCGCCTGCCTTGGCCTCCCTG A G SPIN1 Ensembl:ENSG00000106723 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1196833629 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109926,RMVar_hsa_circ_91298,RMVar_hsa_circ_257656,RMVar_hsa_circ_257657 11123 RMVar_ID_11123 Human_SNP_ID_405988730 A-to-I Human chr9 + 88398808 88398808 88398808 GTTGGTCAGGCTGGTCTTGAACTCCCCACCTCAGGTCATCCGCCTGCCTTGGCCTCCCTGGGATT GTTGGTCAGGCTGGTCTTGAACTCCCCACCTCCGGTCATCCGCCTGCCTTGGCCTCCCTGGGATT A C SPIN1 Ensembl:ENSG00000106723 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1056371131 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109926,RMVar_hsa_circ_91298,RMVar_hsa_circ_257656,RMVar_hsa_circ_257657 11124 RMVar_ID_11124 Human_SNP_ID_405991150 A-to-I Human chr9 + 88406384 88406384 88406384 GCAGACTCGGTTCACTGCAAGCTCCGCCTCCCAGGTTCACACCATTCTCCTGCCTCAGCCTCCCC GCAGACTCGGTTCACTGCAAGCTCCGCCTCCCGGGTTCACACCATTCTCCTGCCTCAGCCTCCCC A G SPIN1 Ensembl:ENSG00000106723 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1228906165 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109926,RMVar_hsa_circ_91298,RMVar_hsa_circ_257656,RMVar_hsa_circ_257657,RMVar_hsa_circ_257659 11125 RMVar_ID_11125 Human_SNP_ID_405991417 A-to-I Human chr9 + 88407347 88407344 88407348 TGTTATTTTCAGTAGAGACAGGGTTTTGCCATATTGCCCAGGCTGGTCTTGAACTGCTGATCCCT TGTTATTTTCAGTAGAGACAGGGTTTTGCC____TGCCCAGGCTGGTCTTGAACTGCTGATCCCT CATAT C SPIN1 Ensembl:ENSG00000106723 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1272499403 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_16726581 RMVar_hsa_circ_109926,RMVar_hsa_circ_91298,RMVar_hsa_circ_257656,RMVar_hsa_circ_257657,RMVar_hsa_circ_257659 11126 RMVar_ID_11126 Human_SNP_ID_405991419 A-to-I Human chr9 + 88407347 88407347 88407347 TGTTATTTTCAGTAGAGACAGGGTTTTGCCATATTGCCCAGGCTGGTCTTGAACTGCTGATCCCT TGTTATTTTCAGTAGAGACAGGGTTTTGCCATGTTGCCCAGGCTGGTCTTGAACTGCTGATCCCT A G SPIN1 Ensembl:ENSG00000106723 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1206631508 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16726581 RMVar_hsa_circ_109926,RMVar_hsa_circ_91298,RMVar_hsa_circ_257656,RMVar_hsa_circ_257657,RMVar_hsa_circ_257659 11127 RMVar_ID_11127 Human_SNP_ID_405996226 A-to-I Human chr9 + 88423797 88423797 88423797 TTATTTATTGTACTTTTTTGAGATGGGGTCTCACTCTGTCATCCAGGCTGGAGTGCAGTGGTGTG TTATTTATTGTACTTTTTTGAGATGGGGTCTCGCTCTGTCATCCAGGCTGGAGTGCAGTGGTGTG A G SPIN1 Ensembl:ENSG00000106723 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1391850111 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116266,RMVar_hsa_circ_109926,RMVar_hsa_circ_91298,RMVar_hsa_circ_257656,RMVar_hsa_circ_257657,RMVar_hsa_circ_257659,RMVar_hsa_circ_301162,RMVar_hsa_circ_257661,RMVar_hsa_circ_106180,RMVar_hsa_circ_313840,RMVar_hsa_circ_332634,RMVar_hsa_circ_257660,RMVar_hsa_circ_317291,RMVar_hsa_circ_298380,RMVar_hsa_circ_257664,RMVar_hsa_circ_257665,RMVar_hsa_circ_257666,RMVar_hsa_circ_257663,RMVar_hsa_circ_257668,RMVar_hsa_circ_271415,RMVar_hsa_circ_257667,RMVar_hsa_circ_300622,RMVar_hsa_circ_257669 11128 RMVar_ID_11128 Human_SNP_ID_405998405 A-to-I Human chr9 + 88431934 88431934 88431934 GTGATGGTGTGTACCTGTAGTTTTAGCTACTCAGGAACCTGAGGTGGGAGGATCACTTTGAGCTC GTGATGGTGTGTACCTGTAGTTTTAGCTACTCGGGAACCTGAGGTGGGAGGATCACTTTGAGCTC A G SPIN1 Ensembl:ENSG00000106723 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1164893016 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7944027 RMVar_hsa_circ_116266,RMVar_hsa_circ_109926,RMVar_hsa_circ_257657,RMVar_hsa_circ_313840,RMVar_hsa_circ_257660,RMVar_hsa_circ_317291,RMVar_hsa_circ_298380,RMVar_hsa_circ_257664,RMVar_hsa_circ_257665,RMVar_hsa_circ_257666,RMVar_hsa_circ_257670,RMVar_hsa_circ_257668,RMVar_hsa_circ_257667,RMVar_hsa_circ_300622,RMVar_hsa_circ_257669,RMVar_hsa_circ_287968,RMVar_hsa_circ_313995,RMVar_hsa_circ_299107,RMVar_hsa_circ_267519,RMVar_hsa_circ_257672,RMVar_hsa_circ_257673,RMVar_hsa_circ_257671 11129 RMVar_ID_11129 Human_SNP_ID_405998406 A-to-I Human chr9 + 88431937 88431937 88431937 ATGGTGTGTACCTGTAGTTTTAGCTACTCAGGAACCTGAGGTGGGAGGATCACTTTGAGCTCAGG ATGGTGTGTACCTGTAGTTTTAGCTACTCAGGGACCTGAGGTGGGAGGATCACTTTGAGCTCAGG A G SPIN1 Ensembl:ENSG00000106723 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs540510635 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7944027 RMVar_hsa_circ_116266,RMVar_hsa_circ_109926,RMVar_hsa_circ_257657,RMVar_hsa_circ_313840,RMVar_hsa_circ_257660,RMVar_hsa_circ_317291,RMVar_hsa_circ_298380,RMVar_hsa_circ_257664,RMVar_hsa_circ_257665,RMVar_hsa_circ_257666,RMVar_hsa_circ_257670,RMVar_hsa_circ_257668,RMVar_hsa_circ_257667,RMVar_hsa_circ_300622,RMVar_hsa_circ_257669,RMVar_hsa_circ_287968,RMVar_hsa_circ_313995,RMVar_hsa_circ_299107,RMVar_hsa_circ_267519,RMVar_hsa_circ_257672,RMVar_hsa_circ_257673,RMVar_hsa_circ_257671 11130 RMVar_ID_11130 Human_SNP_ID_406009695 A-to-I Human chr9 + 88471964 88471964 88471964 GGGATTACAGGCATACGCCACCACATTGGGCTAACTTTCGTATTTTTAGTAGAGATGGGGTTTTG GGGATTACAGGCATACGCCACCACATTGGGCTCACTTTCGTATTTTTAGTAGAGATGGGGTTTTG A C SPIN1 Ensembl:ENSG00000106723 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1428243505 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_257665,RMVar_hsa_circ_257666,RMVar_hsa_circ_257670,RMVar_hsa_circ_257667,RMVar_hsa_circ_267519,RMVar_hsa_circ_257675,RMVar_hsa_circ_94836,RMVar_hsa_circ_257677 11131 RMVar_ID_11131 Human_SNP_ID_406024306 A-to-I Human chr9 - 88528017 88528017 88528017 GCAAAATAAAAATGCAGAGCCCCTTGTTCAAAAAGCAGGAAAAGAATGGGCCAGCAAAGGAACTA GCAAAATAAAAATGCAGAGCCCCTTGTTCAAATAGCAGGAAAAGAATGGGCCAGCAAAGGAACTA T A lnc-SHC3-10,lnc-SHC3-10:2,lnc-SHC3-10:3,lnc-SHC3-10:4,lnc-SHC3-10:5 RNACentral:URS0000D570E3,RNACentral:URS0000D588A7,RNACentral:URS0000D59A47,RNACentral:URS0000D57EFF,RNACentral:URS0000D56CF8 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1018325623 Functional Loss SNV dbSNP153 33..33 33 - - - 11132 RMVar_ID_11132 Human_SNP_ID_406028504 A-to-I Human chr9 + 88543290 88543290 88543290 ATGGAATTTTAACTTTTTTTTTTTTTTTCCTTAGAAATGGGGTCTGCCGCCCAGGCTGGAATGTA ATGGAATTTTAACTTTTTTTTTTTTTTTCCTTTGAAATGGGGTCTGCCGCCCAGGCTGGAATGTA A T NXNL2 Ensembl:ENSG00000130045 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1445419207 Functional Loss SNV dbSNP153 33..33 33 - - - 11133 RMVar_ID_11133 Human_SNP_ID_406247606 A-to-I Human chr9 - 89431590 89431590 89431590 AGGAGGCTGAGGTGGGAGGATCACTTGAGCCCAGGAGCTCAAGGCTGCAGTGAGCTATGATTGCA AGGAGGCTGAGGTGGGAGGATCACTTGAGCCCGGGAGCTCAAGGCTGCAGTGAGCTATGATTGCA T C SEMA4D Ensembl:ENSG00000187764 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs912959127 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125831,RMVar_hsa_circ_257716 11134 RMVar_ID_11134 Human_SNP_ID_406247607 A-to-I Human chr9 - 89431600 89431600 89431600 CTAGCTACTCAGGAGGCTGAGGTGGGAGGATCACTTGAGCCCAGGAGCTCAAGGCTGCAGTGAGC CTAGCTACTCAGGAGGCTGAGGTGGGAGGATCTCTTGAGCCCAGGAGCTCAAGGCTGCAGTGAGC T A SEMA4D Ensembl:ENSG00000187764 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs900626870 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125831,RMVar_hsa_circ_257716 11135 RMVar_ID_11135 Human_SNP_ID_226508296 A-to-I Human chr5 + 30365609 30365609 30365609 TAGCATGTTCTTCCCCACAGGGAGCTTGGAGCACGAGCGGCTGGAGACCTCGCTGAGGATGCAGG TAGCATGTTCTTCCCCACAGGGAGCTTGGAGCTCGAGCGGCTGGAGACCTCGCTGAGGATGCAGG A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917793034 Functional Loss SNV dbSNP153 33..33 33 - - - 11136 RMVar_ID_11136 Human_SNP_ID_226765921 A-to-I Human chr5 - 31405268 31405268 31405268 CCGGTCCAGGTGTCAGGTGATTCTCCTGCCTCAGCCTCCCCAGTAGCTGGGATTACAGGTGCCTC CCGGTCCAGGTGTCAGGTGATTCTCCTGCCTCTGCCTCCCCAGTAGCTGGGATTACAGGTGCCTC T A DROSHA Ensembl:ENSG00000113360 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs761341290 Functional Loss SNV dbSNP153 33..33 33 - - - 11137 RMVar_ID_11137 Human_SNP_ID_226765922 A-to-I Human chr5 - 31405268 31405268 31405268 CCGGTCCAGGTGTCAGGTGATTCTCCTGCCTCAGCCTCCCCAGTAGCTGGGATTACAGGTGCCTC CCGGTCCAGGTGTCAGGTGATTCTCCTGCCTCGGCCTCCCCAGTAGCTGGGATTACAGGTGCCTC T C DROSHA Ensembl:ENSG00000113360 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs761341290 Functional Loss SNV dbSNP153 33..33 33 - - - 11138 RMVar_ID_11138 Human_SNP_ID_226781207 A-to-I Human chr5 - 31474544 31474544 31474544 GCCTGGGCAACATAATTAGACCCTGTCTCTACAAAAAAATTAAAAAAGTAGCCAGGCCTGGTGGC GCCTGGGCAACATAATTAGACCCTGTCTCTACCAAAAAATTAAAAAAGTAGCCAGGCCTGGTGGC T G DROSHA Ensembl:ENSG00000113360 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1318433206 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101864,RMVar_hsa_circ_230606,RMVar_hsa_circ_372842,RMVar_hsa_circ_106761,RMVar_hsa_circ_230613,RMVar_hsa_circ_82552,RMVar_hsa_circ_110269,RMVar_hsa_circ_230620,RMVar_hsa_circ_230621,RMVar_hsa_circ_127111,RMVar_hsa_circ_4417,RMVar_hsa_circ_230626,RMVar_hsa_circ_25483,RMVar_hsa_circ_230625,RMVar_hsa_circ_99921,RMVar_hsa_circ_2478,RMVar_hsa_circ_230629,RMVar_hsa_circ_102642,RMVar_hsa_circ_230633,RMVar_hsa_circ_319375,RMVar_hsa_circ_230634,RMVar_hsa_circ_2009,RMVar_hsa_circ_375699,RMVar_hsa_circ_230640,RMVar_hsa_circ_15992,RMVar_hsa_circ_268220,RMVar_hsa_circ_327275,RMVar_hsa_circ_91989,RMVar_hsa_circ_230642 11139 RMVar_ID_11139 Human_SNP_ID_226795599 A-to-I Human chr5 + 31535822 31535822 31535822 CATTTTTCACATGTAATATGGTTTCATCCCACATGGGCTCAGCAGATCAGAGAGGGCAGACACCA CATTTTTCACATGTAATATGGTTTCATCCCACGTGGGCTCAGCAGATCAGAGAGGGCAGACACCA A G C5orf22 Ensembl:ENSG00000082213 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs777201268 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1041182,Human_RBP_ID_7427881,Human_RBP_ID_8889284,Human_RBP_ID_15422529,Human_RBP_ID_17413396 Human_Splice_Rec_640374,Human_Splice_Rec_640375,Human_Splice_Rec_640390,Human_Splice_Rec_640391,Human_Splice_Rec_640408,Human_Splice_Rec_640409,Human_Splice_Rec_640414,Human_Splice_Rec_640415,Human_Splice_Rec_640420,Human_Splice_Rec_640421,Human_Splice_Rec_640436,Human_Splice_Rec_640437 Human_miRNA_ID_734438,Human_miRNA_ID_2297075 RMVar_hsa_circ_294018,RMVar_hsa_circ_28291,RMVar_hsa_circ_90928,RMVar_hsa_circ_366670,RMVar_hsa_circ_230653,RMVar_hsa_circ_360033,RMVar_hsa_circ_3752,RMVar_hsa_circ_273555,RMVar_hsa_circ_230654 11140 RMVar_ID_11140 Human_SNP_ID_226800097 A-to-I Human chr5 + 31555289 31555289 31555289 CACGAGGTTAGGAGATCGAGACCATACTGGTTAACACGGTGAAACCCCGTCTCCACCAAAAATAC CACGAGGTTAGGAGATCGAGACCATACTGGTTTACACGGTGAAACCCCGTCTCCACCAAAAATAC A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs995475327 Functional Loss SNV dbSNP153 33..33 33 - - - 11141 RMVar_ID_11141 Human_SNP_ID_226811932 A-to-I Human chr5 + 31601547 31601547 31601547 GGGCTTGGTGGCGGGCGCCTGTGGTCCCGGCTACTCGGGAGGCTGAGGCGGGAGAGTGGCATGAA GGGCTTGGTGGCGGGCGCCTGTGGTCCCGGCTTCTCGGGAGGCTGAGGCGGGAGAGTGGCATGAA A T RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1019920573 Functional Loss SNV dbSNP153 33..33 33 - - - 11142 RMVar_ID_11142 Human_SNP_ID_226917424 A-to-I Human chr5 + 32021481 32021481 32021481 ACCATGCCTGGGTGATTTTTGTATTTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGG ACCATGCCTGGGTGATTTTTGTATTTTTTAGTGGAGATGGGGTTTCACCATGTTGGCCAGGCTGG A G PDZD2 Ensembl:ENSG00000133401 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs758994978 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28070,RMVar_hsa_circ_72136,RMVar_hsa_circ_338477 11143 RMVar_ID_11143 Human_SNP_ID_226943555 A-to-I Human chr5 - 32118622 32118622 32118622 TGAGAACAAGATCTCACTCTGTTGCCCAGGCTAGAGTGCAGTGGCCTGATCATGGCTCGTTGCAG TGAGAACAAGATCTCACTCTGTTGCCCAGGCTGGAGTGCAGTGGCCTGATCATGGCTCGTTGCAG T C AC025178.2 Ensembl:ENSG00000250764 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910800520 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5250687 11144 RMVar_ID_11144 Human_SNP_ID_226948309 A-to-I Human chr5 - 32137572 32137572 32137572 TCACTGCAGCCTCCACCTCCTGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGT TCACTGCAGCCTCCACCTCCTGGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGT T C GOLPH3 Ensembl:ENSG00000113384 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs781473646 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109686,RMVar_hsa_circ_230663,RMVar_hsa_circ_119773,RMVar_hsa_circ_230665,RMVar_hsa_circ_230666,RMVar_hsa_circ_285040,RMVar_hsa_circ_230668 11145 RMVar_ID_11145 Human_SNP_ID_226956213 A-to-I Human chr5 - 32164681 32164681 32164681 GTGAAAGAATCGTACTCTTGGCCGGGCGCGGTAGCTCACCCCTGTAATCCCAACACTTTGGGAGT GTGAAAGAATCGTACTCTTGGCCGGGCGCGGTGGCTCACCCCTGTAATCCCAACACTTTGGGAGT T C GOLPH3 Ensembl:ENSG00000113384 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1458577655 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15424788,Human_RBP_ID_17575621,Human_RBP_ID_22727692 RMVar_hsa_circ_109686,RMVar_hsa_circ_230666,RMVar_hsa_circ_230671 11146 RMVar_ID_11146 Human_SNP_ID_226956337 A-to-I Human chr5 - 32165048 32165048 32165048 TAAAAATACAAAAATTAGCCAGGCAGGGTGGTATGCACCTGAAATCCCAGCTACTCGGGAGGCTG TAAAAATACAAAAATTAGCCAGGCAGGGTGGTGTGCACCTGAAATCCCAGCTACTCGGGAGGCTG T C GOLPH3 Ensembl:ENSG00000113384 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1184850074 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109686,RMVar_hsa_circ_230666,RMVar_hsa_circ_230671 11147 RMVar_ID_11147 Human_SNP_ID_226956737 A-to-I Human chr5 - 32166590 32166590 32166590 TTGGCCAGGCTGGTCTCGAACTCTTGACCTCAAGTGATCCGCCCACCTCGCCTTCCCAAAGGTCT TTGGCCAGGCTGGTCTCGAACTCTTGACCTCAGGTGATCCGCCCACCTCGCCTTCCCAAAGGTCT T C GOLPH3 Ensembl:ENSG00000113384 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1212332118 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109686,RMVar_hsa_circ_230666,RMVar_hsa_circ_230671 11148 RMVar_ID_11148 Human_SNP_ID_226957086 A-to-I Human chr5 - 32167730 32167730 32167730 TGTTGCCTAGTCTCGAACTCCTGGCCTCAAGCAATCTTCCCGCCTTGGCCTCCCAAAGTTCTGGG TGTTGCCTAGTCTCGAACTCCTGGCCTCAAGCGATCTTCCCGCCTTGGCCTCCCAAAGTTCTGGG T C GOLPH3 Ensembl:ENSG00000113384 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs112114069 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8613800,Human_RBP_ID_15424899,Human_RBP_ID_25889178 RMVar_hsa_circ_109686,RMVar_hsa_circ_230666,RMVar_hsa_circ_230671 11149 RMVar_ID_11149 Human_SNP_ID_226957129 A-to-I Human chr5 - 32167871 32167871 32167871 TGGCTCATTGCAACCTCGACCTCCTGAACTCAAGCAATCCTCCCTCCTCAGTCTCCTGAATAGCT TGGCTCATTGCAACCTCGACCTCCTGAACTCAGGCAATCCTCCCTCCTCAGTCTCCTGAATAGCT T C GOLPH3 Ensembl:ENSG00000113384 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1372644858 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2924997 RMVar_hsa_circ_109686,RMVar_hsa_circ_230666,RMVar_hsa_circ_230671 11150 RMVar_ID_11150 Human_SNP_ID_226957139 A-to-I Human chr5 - 32167904 32167904 32167904 TGTCTTCCAGACTGGAGTGTGGTGGTGTGATCATGGCTCATTGCAACCTCGACCTCCTGAACTCA TGTCTTCCAGACTGGAGTGTGGTGGTGTGATCGTGGCTCATTGCAACCTCGACCTCCTGAACTCA T C GOLPH3 Ensembl:ENSG00000113384 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1182290906 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15424906 RMVar_hsa_circ_109686,RMVar_hsa_circ_230666,RMVar_hsa_circ_230671 11151 RMVar_ID_11151 Human_SNP_ID_226973064 A-to-I Human chr5 - 32228643 32228632 32228643 CTTCTTGGATCTGCTGTCTAAATGATATATATATGATATATATGTGATATATATATATCATATAT CTTCTTGGATCTGCTGTCTAAATGATATATAT___________GTGATATATATATATCATATAT CATATATATCAT C MTMR12 Ensembl:ENSG00000150712 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1436647695 Functional Loss DEL dbSNP153 33..43 33 - - - Human_RBP_ID_18047017 Human_miRNA_ID_355542,Human_miRNA_ID_1403291 11152 RMVar_ID_11152 Human_SNP_ID_226973072 A-to-I Human chr5 - 32228643 32228643 32228643 CTTCTTGGATCTGCTGTCTAAATGATATATATATGATATATATGTGATATATATATATCATATAT CTTCTTGGATCTGCTGTCTAAATGATATATATGTGATATATATGTGATATATATATATCATATAT T C MTMR12 Ensembl:ENSG00000150712 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs989977154 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18047017 Human_miRNA_ID_355542,Human_miRNA_ID_1403291 11153 RMVar_ID_11153 Human_SNP_ID_226976946 A-to-I Human chr5 - 32244509 32244509 32244509 TTAGCTCACTGTAACCTCCGCCACCCTGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTGGC TTAGCTCACTGTAACCTCCGCCACCCTGGTTCGAGCAATTCTCCTGCCTCAGCCTCCCAAGTGGC T C MTMR12 Ensembl:ENSG00000150712 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1370725115 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4738,RMVar_hsa_circ_70672,RMVar_hsa_circ_71145,RMVar_hsa_circ_108616,RMVar_hsa_circ_317604,RMVar_hsa_circ_69161,RMVar_hsa_circ_230674,RMVar_hsa_circ_38526,RMVar_hsa_circ_309512,RMVar_hsa_circ_42098,RMVar_hsa_circ_63585,RMVar_hsa_circ_230675,RMVar_hsa_circ_230676 11154 RMVar_ID_11154 Human_SNP_ID_226976947 A-to-I Human chr5 - 32244509 32244509 32244509 TTAGCTCACTGTAACCTCCGCCACCCTGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTGGC TTAGCTCACTGTAACCTCCGCCACCCTGGTTCCAGCAATTCTCCTGCCTCAGCCTCCCAAGTGGC T G MTMR12 Ensembl:ENSG00000150712 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1370725115 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4738,RMVar_hsa_circ_70672,RMVar_hsa_circ_71145,RMVar_hsa_circ_108616,RMVar_hsa_circ_317604,RMVar_hsa_circ_69161,RMVar_hsa_circ_230674,RMVar_hsa_circ_38526,RMVar_hsa_circ_309512,RMVar_hsa_circ_42098,RMVar_hsa_circ_63585,RMVar_hsa_circ_230675,RMVar_hsa_circ_230676 11155 RMVar_ID_11155 Human_SNP_ID_227006838 A-to-I Human chr5 - 32364698 32364698 32364698 TCTCACTCCATCACTCAGGGTGCTAGAGTGCAATGGCGCAATCTCAGCTTACTGCAGCCAGTAAA TCTCACTCCATCACTCAGGGTGCTAGAGTGCAGTGGCGCAATCTCAGCTTACTGCAGCCAGTAAA T C ZFR Ensembl:ENSG00000056097 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1234962598 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15426042 RMVar_hsa_circ_1402,RMVar_hsa_circ_275507,RMVar_hsa_circ_314113,RMVar_hsa_circ_356928,RMVar_hsa_circ_368234,RMVar_hsa_circ_51174,RMVar_hsa_circ_59059,RMVar_hsa_circ_49831,RMVar_hsa_circ_230692,RMVar_hsa_circ_230693 11156 RMVar_ID_11156 Human_SNP_ID_227007540 A-to-I Human chr5 - 32367567 32367567 32367567 TCTACTAAAAATAAAAATTAGCCAAGCATGGTAGTGGGTTCTGTAGTGCCAGCTACTCAGGAGGC TCTACTAAAAATAAAAATTAGCCAAGCATGGTGGTGGGTTCTGTAGTGCCAGCTACTCAGGAGGC T C ZFR Ensembl:ENSG00000056097 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1342732176 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1402,RMVar_hsa_circ_275507,RMVar_hsa_circ_314113,RMVar_hsa_circ_356928,RMVar_hsa_circ_368234,RMVar_hsa_circ_51174,RMVar_hsa_circ_59059,RMVar_hsa_circ_49831,RMVar_hsa_circ_230692,RMVar_hsa_circ_230693 11157 RMVar_ID_11157 Human_SNP_ID_227007551 A-to-I Human chr5 - 32367633 32367633 32367633 AAGATGGAAAGATCACTTGAGCCCAGGAGTTCAAGACCAGCTCAGGCAACATAGCAAGACCTCAT AAGATGGAAAGATCACTTGAGCCCAGGAGTTCGAGACCAGCTCAGGCAACATAGCAAGACCTCAT T C ZFR Ensembl:ENSG00000056097 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1473806595 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1402,RMVar_hsa_circ_275507,RMVar_hsa_circ_314113,RMVar_hsa_circ_356928,RMVar_hsa_circ_368234,RMVar_hsa_circ_51174,RMVar_hsa_circ_59059,RMVar_hsa_circ_49831,RMVar_hsa_circ_230692,RMVar_hsa_circ_230693 11158 RMVar_ID_11158 Human_SNP_ID_227007664 A-to-I Human chr5 - 32368094 32368094 32368094 GTTTTACATAGGTCTTTGTCTCTACCAGAGCTAGAAACTAATATTCATGGAAACTAGTTAATGTT GTTTTACATAGGTCTTTGTCTCTACCAGAGCTTGAAACTAATATTCATGGAAACTAGTTAATGTT T A ZFR Ensembl:ENSG00000056097 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2032888 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10201137,Human_RBP_ID_25889413 GWAS_ID_974,GWAS_ID_975 RMVar_hsa_circ_1402,RMVar_hsa_circ_275507,RMVar_hsa_circ_314113,RMVar_hsa_circ_356928,RMVar_hsa_circ_368234,RMVar_hsa_circ_51174,RMVar_hsa_circ_59059,RMVar_hsa_circ_49831,RMVar_hsa_circ_230692,RMVar_hsa_circ_230693 11159 RMVar_ID_11159 Human_SNP_ID_227007665 A-to-I Human chr5 - 32368094 32368094 32368094 GTTTTACATAGGTCTTTGTCTCTACCAGAGCTAGAAACTAATATTCATGGAAACTAGTTAATGTT GTTTTACATAGGTCTTTGTCTCTACCAGAGCTGGAAACTAATATTCATGGAAACTAGTTAATGTT T C ZFR Ensembl:ENSG00000056097 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2032888 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10201137,Human_RBP_ID_25889413 GWAS_ID_974,GWAS_ID_975 RMVar_hsa_circ_1402,RMVar_hsa_circ_275507,RMVar_hsa_circ_314113,RMVar_hsa_circ_356928,RMVar_hsa_circ_368234,RMVar_hsa_circ_51174,RMVar_hsa_circ_59059,RMVar_hsa_circ_49831,RMVar_hsa_circ_230692,RMVar_hsa_circ_230693 11160 RMVar_ID_11160 Human_SNP_ID_227010195 A-to-I Human chr5 - 32377370 32377370 32377370 CAAGACTGCCCTGACCAACATGCACACCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAA CAAGACTGCCCTGACCAACATGCACACCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAA T C ZFR Ensembl:ENSG00000056097 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs925008928 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1402,RMVar_hsa_circ_275507,RMVar_hsa_circ_314113,RMVar_hsa_circ_356928,RMVar_hsa_circ_368234,RMVar_hsa_circ_51174,RMVar_hsa_circ_59059,RMVar_hsa_circ_49831,RMVar_hsa_circ_230692,RMVar_hsa_circ_230693 11161 RMVar_ID_11161 Human_SNP_ID_227011367 A-to-I Human chr5 - 32382051 32382051 32382051 ATGATCCACCTGCCTCAGCCTCCCAAAGTGCTAGGATTACAGGCATGAGCCACTGCACCTGGCCC ATGATCCACCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGCACCTGGCCC T C ZFR Ensembl:ENSG00000056097 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1203185733 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1402,RMVar_hsa_circ_275507,RMVar_hsa_circ_314113,RMVar_hsa_circ_356928,RMVar_hsa_circ_368234,RMVar_hsa_circ_51174,RMVar_hsa_circ_49831,RMVar_hsa_circ_281741,RMVar_hsa_circ_353033,RMVar_hsa_circ_230692,RMVar_hsa_circ_230693,RMVar_hsa_circ_358867,RMVar_hsa_circ_329048,RMVar_hsa_circ_285822,RMVar_hsa_circ_49716,RMVar_hsa_circ_276291,RMVar_hsa_circ_230695,RMVar_hsa_circ_230696 11162 RMVar_ID_11162 Human_SNP_ID_227011394 A-to-I Human chr5 - 32382146 32382146 32382146 GGCATGTGCCACGACACCCAGCTAATTTTTGTATTTTTGAGTAGGAATGGAGTTTCACCATGTTG GGCATGTGCCACGACACCCAGCTAATTTTTGTGTTTTTGAGTAGGAATGGAGTTTCACCATGTTG T C ZFR Ensembl:ENSG00000056097 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941380385 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15426520,Human_RBP_ID_25889584 RMVar_hsa_circ_1402,RMVar_hsa_circ_275507,RMVar_hsa_circ_314113,RMVar_hsa_circ_356928,RMVar_hsa_circ_368234,RMVar_hsa_circ_51174,RMVar_hsa_circ_49831,RMVar_hsa_circ_281741,RMVar_hsa_circ_353033,RMVar_hsa_circ_230692,RMVar_hsa_circ_230693,RMVar_hsa_circ_358867,RMVar_hsa_circ_329048,RMVar_hsa_circ_285822,RMVar_hsa_circ_49716,RMVar_hsa_circ_276291,RMVar_hsa_circ_230695,RMVar_hsa_circ_230696 11163 RMVar_ID_11163 Human_SNP_ID_227011432 A-to-I Human chr5 - 32382305 32382305 32382305 GAGGGGTTTGGTTTTGTTTTGCTTTGTTTTTGAGACAGTCACTCTGTCACCCAGGCTGGAGTGCA GAGGGGTTTGGTTTTGTTTTGCTTTGTTTTTGGGACAGTCACTCTGTCACCCAGGCTGGAGTGCA T C ZFR Ensembl:ENSG00000056097 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs890124521 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7429445,Human_RBP_ID_15426525 RMVar_hsa_circ_1402,RMVar_hsa_circ_275507,RMVar_hsa_circ_314113,RMVar_hsa_circ_356928,RMVar_hsa_circ_368234,RMVar_hsa_circ_51174,RMVar_hsa_circ_49831,RMVar_hsa_circ_281741,RMVar_hsa_circ_353033,RMVar_hsa_circ_230692,RMVar_hsa_circ_230693,RMVar_hsa_circ_358867,RMVar_hsa_circ_329048,RMVar_hsa_circ_285822,RMVar_hsa_circ_49716,RMVar_hsa_circ_276291,RMVar_hsa_circ_230695,RMVar_hsa_circ_230696 11164 RMVar_ID_11164 Human_SNP_ID_227013795 A-to-I Human chr5 - 32391922 32391922 32391922 TGAGACCAGCCTAGGCAACATGACAAGACCCCATCTCTACAAAAAATACGAAAATTAGCTGGGCG TGAGACCAGCCTAGGCAACATGACAAGACCCCTTCTCTACAAAAAATACGAAAATTAGCTGGGCG T A ZFR Ensembl:ENSG00000056097 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2963975 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_976,GWAS_ID_977,GWAS_ID_978,GWAS_ID_979,GWAS_ID_980,GWAS_ID_981,GWAS_ID_982,GWAS_ID_983,GWAS_ID_984,GWAS_ID_985,GWAS_ID_986,GWAS_ID_987,GWAS_ID_988 RMVar_hsa_circ_314113,RMVar_hsa_circ_368234,RMVar_hsa_circ_51174,RMVar_hsa_circ_49831,RMVar_hsa_circ_353033,RMVar_hsa_circ_358867,RMVar_hsa_circ_329048,RMVar_hsa_circ_49716,RMVar_hsa_circ_276291,RMVar_hsa_circ_301711,RMVar_hsa_circ_265272,RMVar_hsa_circ_265158,RMVar_hsa_circ_366587,RMVar_hsa_circ_336879,RMVar_hsa_circ_272304,RMVar_hsa_circ_230698 11165 RMVar_ID_11165 Human_SNP_ID_227013796 A-to-I Human chr5 - 32391922 32391922 32391922 TGAGACCAGCCTAGGCAACATGACAAGACCCCATCTCTACAAAAAATACGAAAATTAGCTGGGCG TGAGACCAGCCTAGGCAACATGACAAGACCCCGTCTCTACAAAAAATACGAAAATTAGCTGGGCG T C ZFR Ensembl:ENSG00000056097 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2963975 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_976,GWAS_ID_977,GWAS_ID_978,GWAS_ID_979,GWAS_ID_980,GWAS_ID_981,GWAS_ID_982,GWAS_ID_983,GWAS_ID_984,GWAS_ID_985,GWAS_ID_986,GWAS_ID_987,GWAS_ID_988 RMVar_hsa_circ_314113,RMVar_hsa_circ_368234,RMVar_hsa_circ_51174,RMVar_hsa_circ_49831,RMVar_hsa_circ_353033,RMVar_hsa_circ_358867,RMVar_hsa_circ_329048,RMVar_hsa_circ_49716,RMVar_hsa_circ_276291,RMVar_hsa_circ_301711,RMVar_hsa_circ_265272,RMVar_hsa_circ_265158,RMVar_hsa_circ_366587,RMVar_hsa_circ_336879,RMVar_hsa_circ_272304,RMVar_hsa_circ_230698 11166 RMVar_ID_11166 Human_SNP_ID_227014155 A-to-I Human chr5 - 32393472 32393472 32393472 CGGCGTGGTGGCGCATGCCTGTAATTCCGGCTACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAA CGGCGTGGTGGCGCATGCCTGTAATTCCGGCTTCTCAGGAGGCTGAGGCAGGAGAATTGCTTGAA T A ZFR Ensembl:ENSG00000056097 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs531924043 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15426902 RMVar_hsa_circ_314113,RMVar_hsa_circ_368234,RMVar_hsa_circ_51174,RMVar_hsa_circ_49831,RMVar_hsa_circ_353033,RMVar_hsa_circ_358867,RMVar_hsa_circ_329048,RMVar_hsa_circ_49716,RMVar_hsa_circ_276291,RMVar_hsa_circ_301711,RMVar_hsa_circ_265272,RMVar_hsa_circ_265158,RMVar_hsa_circ_366587,RMVar_hsa_circ_336879,RMVar_hsa_circ_272304,RMVar_hsa_circ_230698 11167 RMVar_ID_11167 Human_SNP_ID_227014156 A-to-I Human chr5 - 32393472 32393472 32393472 CGGCGTGGTGGCGCATGCCTGTAATTCCGGCTACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAA CGGCGTGGTGGCGCATGCCTGTAATTCCGGCTGCTCAGGAGGCTGAGGCAGGAGAATTGCTTGAA T C ZFR Ensembl:ENSG00000056097 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs531924043 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15426902 RMVar_hsa_circ_314113,RMVar_hsa_circ_368234,RMVar_hsa_circ_51174,RMVar_hsa_circ_49831,RMVar_hsa_circ_353033,RMVar_hsa_circ_358867,RMVar_hsa_circ_329048,RMVar_hsa_circ_49716,RMVar_hsa_circ_276291,RMVar_hsa_circ_301711,RMVar_hsa_circ_265272,RMVar_hsa_circ_265158,RMVar_hsa_circ_366587,RMVar_hsa_circ_336879,RMVar_hsa_circ_272304,RMVar_hsa_circ_230698 11168 RMVar_ID_11168 Human_SNP_ID_227019124 A-to-I Human chr5 - 32411807 32411807 32411807 GTACATCCTCTTAAATATGTTAAATTATCTCTAGATTACTTACAGTACCTAATACCATGTAAGTG GTACATCCTCTTAAATATGTTAAATTATCTCTGGATTACTTACAGTACCTAATACCATGTAAGTG T C ZFR Ensembl:ENSG00000056097 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1408665641 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10201384 RMVar_hsa_circ_314113,RMVar_hsa_circ_49831,RMVar_hsa_circ_329048,RMVar_hsa_circ_276291,RMVar_hsa_circ_51579,RMVar_hsa_circ_364596,RMVar_hsa_circ_362915,RMVar_hsa_circ_311719,RMVar_hsa_circ_306342,RMVar_hsa_circ_230699,RMVar_hsa_circ_299906,RMVar_hsa_circ_230701 11169 RMVar_ID_11169 Human_SNP_ID_227022238 A-to-I Human chr5 - 32422652 32422652 32422652 GGGACTACAGGCACACACTACCATGTGTGGCTAATTTTTAAAAAATTTTCTGTAGAGATGTGGTC GGGACTACAGGCACACACTACCATGTGTGGCTGATTTTTAAAAAATTTTCTGTAGAGATGTGGTC T C ZFR Ensembl:ENSG00000056097 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991429371 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15427707 RMVar_hsa_circ_49831 11170 RMVar_ID_11170 Human_SNP_ID_227023078 A-to-I Human chr5 - 32425665 32425665 32425665 AAAAATTAGCCAGAAGGTGGCAGCTGCCTGTAATCCCAGCTACTCGGGTGGCTGAGGCAGGGAAA AAAAATTAGCCAGAAGGTGGCAGCTGCCTGTATTCCCAGCTACTCGGGTGGCTGAGGCAGGGAAA T A ZFR Ensembl:ENSG00000056097 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1477969226 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49831 11171 RMVar_ID_11171 Human_SNP_ID_227024243 A-to-I Human chr5 - 32430077 32430077 32430077 TATCGTGATTTTTTTTTTTTTTTTTTTTTTGAAATAGGGTCTCACTCTGTCACCCAGGCTACATC TATCGTGATTTTTTTTTTTTTTTTTTTTTTGATATAGGGTCTCACTCTGTCACCCAGGCTACATC T A ZFR Ensembl:ENSG00000056097 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1367779089 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15428215 RMVar_hsa_circ_49831 11172 RMVar_ID_11172 Human_SNP_ID_227024244 A-to-I Human chr5 - 32430077 32430077 32430077 TATCGTGATTTTTTTTTTTTTTTTTTTTTTGAAATAGGGTCTCACTCTGTCACCCAGGCTACATC TATCGTGATTTTTTTTTTTTTTTTTTTTTTGAGATAGGGTCTCACTCTGTCACCCAGGCTACATC T C ZFR Ensembl:ENSG00000056097 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1367779089 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15428215 RMVar_hsa_circ_49831 11173 RMVar_ID_11173 Human_SNP_ID_227024892 A-to-I Human chr5 - 32432288 32432288 32432288 AATTTTTTATTCCGTATTGCCCTGAAAGGTATATGGACTGTGTTCTCTAAATACAACTAACTGTT AATTTTTTATTCCGTATTGCCCTGAAAGGTATGTGGACTGTGTTCTCTAAATACAACTAACTGTT T C ZFR Ensembl:ENSG00000056097 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs531521159 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15428345 RMVar_hsa_circ_49831 11174 RMVar_ID_11174 Human_SNP_ID_227024904 A-to-I Human chr5 - 32432324 32432324 32432324 CATTTAGTGAGCTATTACCTACATTATAGTAAACCCAATTTTTTATTCCGTATTGCCCTGAAAGG CATTTAGTGAGCTATTACCTACATTATAGTAAGCCCAATTTTTTATTCCGTATTGCCCTGAAAGG T C ZFR Ensembl:ENSG00000056097 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1370459441 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7430031,Human_RBP_ID_15428348 RMVar_hsa_circ_49831 11175 RMVar_ID_11175 Human_SNP_ID_227024905 A-to-I Human chr5 - 32432326 32432326 32432326 CACATTTAGTGAGCTATTACCTACATTATAGTAAACCCAATTTTTTATTCCGTATTGCCCTGAAA CACATTTAGTGAGCTATTACCTACATTATAGTGAACCCAATTTTTTATTCCGTATTGCCCTGAAA T C ZFR Ensembl:ENSG00000056097 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs987483981 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7430031,Human_RBP_ID_15428348 RMVar_hsa_circ_49831 11176 RMVar_ID_11176 Human_SNP_ID_227025044 A-to-I Human chr5 - 32432826 32432826 32432826 TACTTAGAAGACTGAGGTAGGAGGATCACGTGAGCTGGGGATGTTGAGGGTGCAGTGAGCTGTGA TACTTAGAAGACTGAGGTAGGAGGATCACGTGGGCTGGGGATGTTGAGGGTGCAGTGAGCTGTGA T C ZFR Ensembl:ENSG00000056097 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1347243025 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7430033,Human_RBP_ID_15428371 RMVar_hsa_circ_49831 11177 RMVar_ID_11177 Human_SNP_ID_227025047 A-to-I Human chr5 - 32432840 32432840 32432840 CCTGTGGTCCCAGCTACTTAGAAGACTGAGGTAGGAGGATCACGTGAGCTGGGGATGTTGAGGGT CCTGTGGTCCCAGCTACTTAGAAGACTGAGGTGGGAGGATCACGTGAGCTGGGGATGTTGAGGGT T C ZFR Ensembl:ENSG00000056097 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs567282550 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49831 11178 RMVar_ID_11178 Human_SNP_ID_227027248 A-to-I Human chr5 - 32441042 32441042 32441042 TTGAACCGGGGAGGTGGAGGTTGCAGTGAGCCAAGATCGCGCGATTACACTCTGGCTGGGCAACA TTGAACCGGGGAGGTGGAGGTTGCAGTGAGCCGAGATCGCGCGATTACACTCTGGCTGGGCAACA T C ZFR Ensembl:ENSG00000056097 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1242222876 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49831 11179 RMVar_ID_11179 Human_SNP_ID_227027283 A-to-I Human chr5 - 32441198 32441198 32441198 CTAAGGCGGGTGTATCACCTGAGGTCAGGGGTATGAGATCAGCCTGACCAACATGGCGAAACCCG CTAAGGCGGGTGTATCACCTGAGGTCAGGGGTTTGAGATCAGCCTGACCAACATGGCGAAACCCG T A ZFR Ensembl:ENSG00000056097 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1022409658 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15428835,Human_RBP_ID_25890398 RMVar_hsa_circ_49831 11180 RMVar_ID_11180 Human_SNP_ID_227027284 A-to-I Human chr5 - 32441198 32441198 32441198 CTAAGGCGGGTGTATCACCTGAGGTCAGGGGTATGAGATCAGCCTGACCAACATGGCGAAACCCG CTAAGGCGGGTGTATCACCTGAGGTCAGGGGTGTGAGATCAGCCTGACCAACATGGCGAAACCCG T C ZFR Ensembl:ENSG00000056097 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1022409658 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15428835,Human_RBP_ID_25890398 RMVar_hsa_circ_49831 11181 RMVar_ID_11181 Human_SNP_ID_227208279 A-to-I Human chr5 + 33162324 33162324 33162324 TGGCCCCCGCCGCATCCACACAGTCCGTGTGCAGGGAAGTAACAAGAAATACCGTGCCCTGAGGT TGGCCCCCGCCGCATCCACACAGTCCGTGTGCGGGGAAGTAACAAGAAATACCGTGCCCTGAGGT A G AC010343.1 Ensembl:ENSG00000240376 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs548437212 Functional Loss SNV dbSNP153 33..33 33 - - - 11182 RMVar_ID_11182 Human_SNP_ID_227418095 A-to-I Human chr5 - 34048573 34048573 34048573 CAGAATTCTTCTCATTGTACCCTGGCAAAGGTATCAGTTTTAGTTGGGCAGTGCCCCCTACACAG CAGAATTCTTCTCATTGTACCCTGGCAAAGGTGTCAGTTTTAGTTGGGCAGTGCCCCCTACACAG T C C1QTNF3-AMACR Ensembl:ENSG00000273294 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1393869716 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56125,RMVar_hsa_circ_230749,RMVar_hsa_circ_230752,RMVar_hsa_circ_289277 11183 RMVar_ID_11183 Human_SNP_ID_227418107 A-to-I Human chr5 - 34048638 34048638 34048638 TCTGAGCAATGGCCCTTAACCCTGGTAGCTATAGTTGGTTCCAGGTCAACTTCTTTCTATATTCC TCTGAGCAATGGCCCTTAACCCTGGTAGCTATCGTTGGTTCCAGGTCAACTTCTTTCTATATTCC T G C1QTNF3-AMACR Ensembl:ENSG00000273294 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs930692244 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56125,RMVar_hsa_circ_230749,RMVar_hsa_circ_230752,RMVar_hsa_circ_289277 11184 RMVar_ID_11184 Human_SNP_ID_227418108 A-to-I Human chr5 - 34048640 34048640 34048640 CATCTGAGCAATGGCCCTTAACCCTGGTAGCTATAGTTGGTTCCAGGTCAACTTCTTTCTATATT CATCTGAGCAATGGCCCTTAACCCTGGTAGCTGTAGTTGGTTCCAGGTCAACTTCTTTCTATATT T C C1QTNF3-AMACR Ensembl:ENSG00000273294 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1205998452 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56125,RMVar_hsa_circ_230749,RMVar_hsa_circ_230752,RMVar_hsa_circ_289277 11185 RMVar_ID_11185 Human_SNP_ID_227418249 A-to-I Human chr5 - 34049238 34049238 34049238 TGAGGAGGGGGAACTGCCCAACTAAAACTGATACCTTTGCCAGGGTACAATGAGGCTAATTCTGG TGAGGAGGGGGAACTGCCCAACTAAAACTGATGCCTTTGCCAGGGTACAATGAGGCTAATTCTGG T C C1QTNF3-AMACR Ensembl:ENSG00000273294 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1448559767 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_168338,Human_RBP_ID_2926305,Human_RBP_ID_17575381,Human_RBP_ID_22727694,Human_RBP_ID_26792050 RMVar_hsa_circ_56125,RMVar_hsa_circ_230749,RMVar_hsa_circ_230752,RMVar_hsa_circ_289277 11186 RMVar_ID_11186 Human_SNP_ID_227418250 A-to-I Human chr5 - 34049250 34049250 34049250 GACTCAGGCTTCTGAGGAGGGGGAACTGCCCAACTAAAACTGATACCTTTGCCAGGGTACAATGA GACTCAGGCTTCTGAGGAGGGGGAACTGCCCAGCTAAAACTGATACCTTTGCCAGGGTACAATGA T C C1QTNF3-AMACR Ensembl:ENSG00000273294 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs540746611 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2926305,Human_RBP_ID_17575381,Human_RBP_ID_22727694,Human_RBP_ID_26792050 RMVar_hsa_circ_56125,RMVar_hsa_circ_230749,RMVar_hsa_circ_230752,RMVar_hsa_circ_289277 11187 RMVar_ID_11187 Human_SNP_ID_227430092 A-to-I Human chr5 - 34103814 34103813 34103814 ATTTGACTACCTTTTTTTTTTTTAGAGACAGAATTTTGCTCTTGTCACCCAGGCTGGAATGCAGT ATTTGACTACCTTTTTTTTTTTTAGAGACAGA_TTTTGCTCTTGTCACCCAGGCTGGAATGCAGT AT A C1QTNF3-AMACR Ensembl:ENSG00000273294 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1175973988 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_56125,RMVar_hsa_circ_289277 11188 RMVar_ID_11188 Human_SNP_ID_227445920 A-to-I Human chr5 - 34175959 34175959 34175959 CAGTTCTTACTCTTCTCTTTGCCTTGATTCCCAGGATCCACCTCTGATGTTCAGTGAAGAGTACC CAGTTCTTACTCTTCTCTTTGCCTTGATTCCCGGGATCCACCTCTGATGTTCAGTGAAGAGTACC T C AC138409.2 Ensembl:ENSG00000215158 Pseudogene intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1283823719 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5611657,Human_RBP_ID_22680354 RMVar_hsa_circ_32031,RMVar_hsa_circ_275459,RMVar_hsa_circ_292957,RMVar_hsa_circ_322601,RMVar_hsa_circ_230760 11189 RMVar_ID_11189 Human_SNP_ID_227598493 A-to-I Human chr5 + 34819800 34819800 34819800 TATTTATTGATTTATTTTAGAGATGGGGTCTTACTGTATTGCCCAGACTGGTCTCAAACTCCTGA TATTTATTGATTTATTTTAGAGATGGGGTCTTCCTGTATTGCCCAGACTGGTCTCAAACTCCTGA A C RAI14 Ensembl:ENSG00000039560 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1032858600 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32419,RMVar_hsa_circ_84569,RMVar_hsa_circ_127467,RMVar_hsa_circ_230766,RMVar_hsa_circ_230767,RMVar_hsa_circ_323304,RMVar_hsa_circ_368664,RMVar_hsa_circ_68994,RMVar_hsa_circ_230774,RMVar_hsa_circ_230773,RMVar_hsa_circ_336330,RMVar_hsa_circ_307835,RMVar_hsa_circ_353874,RMVar_hsa_circ_306930,RMVar_hsa_circ_230777,RMVar_hsa_circ_230778,RMVar_hsa_circ_314788,RMVar_hsa_circ_230780,RMVar_hsa_circ_356022,RMVar_hsa_circ_230779,RMVar_hsa_circ_367804,RMVar_hsa_circ_316953 11190 RMVar_ID_11190 Human_SNP_ID_227613860 A-to-I Human chr5 - 34885654 34885654 34885654 AGCCTTGACCTCCCAGGCTCAAATGATCCTCTACGTCAGCCTCTAAAGTAGCTGGGACTATAGTT AGCCTTGACCTCCCAGGCTCAAATGATCCTCTGCGTCAGCCTCTAAAGTAGCTGGGACTATAGTT T C RF00017-4494 RNACentral:URS00009086DB SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444215907 Functional Loss SNV dbSNP153 33..33 33 - - - 11191 RMVar_ID_11191 Human_SNP_ID_227613863 A-to-I Human chr5 - 34885665 34885665 34885665 AGGGCTCATGTAGCCTTGACCTCCCAGGCTCAAATGATCCTCTACGTCAGCCTCTAAAGTAGCTG AGGGCTCATGTAGCCTTGACCTCCCAGGCTCAGATGATCCTCTACGTCAGCCTCTAAAGTAGCTG T C RF00017-4494 RNACentral:URS00009086DB SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1412855145 Functional Loss SNV dbSNP153 33..33 33 - - - 11192 RMVar_ID_11192 Human_SNP_ID_227616517 A-to-I Human chr5 - 34897159 34897159 34897159 GCTGGTCTCGAACTCCTGAGCTCAGACAATCCACCTGCCTCAGCCTCTGAAAGTGCTAGGATTAC GCTGGTCTCGAACTCCTGAGCTCAGACAATCCGCCTGCCTCAGCCTCTGAAAGTGCTAGGATTAC T C RF00017-4494 RNACentral:URS00009086DB SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs539361654 Functional Loss SNV dbSNP153 33..33 33 - - - 11193 RMVar_ID_11193 Human_SNP_ID_227618216 A-to-I Human chr5 - 34904361 34904361 34904361 TCGATCTTTTGACCTTGTGATCCTCCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG TCGATCTTTTGACCTTGTGATCCTCCTGCCTCCGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG T G RF00017-4494,lnc-RAD1-1 RNACentral:URS00009086DB,RNACentral:URS00008B62E3 SRP RNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1191859955 Functional Loss SNV dbSNP153 33..33 33 - - - 11194 RMVar_ID_11194 Human_SNP_ID_227618241 A-to-I Human chr5 - 34904472 34904472 34904472 CTCCTGCCTCAGCCTCCCGAGTAGTTGGGACTACAGGTGCATGCCACCACATCGAGCTAATAATT CTCCTGCCTCAGCCTCCCGAGTAGTTGGGACTGCAGGTGCATGCCACCACATCGAGCTAATAATT T C RF00017-4494,lnc-RAD1-1 RNACentral:URS00009086DB,RNACentral:URS00008B62E3 SRP RNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs776467975 Functional Loss SNV dbSNP153 33..33 33 - - - 11195 RMVar_ID_11195 Human_SNP_ID_227618599 A-to-I Human chr5 - 34906065 34906065 34906065 CTGTAATCCCAGCTACTTGAGAGGCTGAGGCAAGAGAATCACTTGAAACTGGAAGGCGGGGGTTG CTGTAATCCCAGCTACTTGAGAGGCTGAGGCAGGAGAATCACTTGAAACTGGAAGGCGGGGGTTG T C RAD1 Ensembl:ENSG00000113456 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1309739986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15433791 11196 RMVar_ID_11196 Human_SNP_ID_227618614 A-to-I Human chr5 - 34906134 34906134 34906134 CTGGCCAACATGGTGAAACCCCTACCTCTACTAAAAATACAAAAATTAGCTGGGTGTGGTGGTGG CTGGCCAACATGGTGAAACCCCTACCTCTACTGAAAATACAAAAATTAGCTGGGTGTGGTGGTGG T C RAD1 Ensembl:ENSG00000113456 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1288241256 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18047468 11197 RMVar_ID_11197 Human_SNP_ID_227618640 A-to-I Human chr5 - 34906236 34906235 34906236 ACTATTATTTTAGGCCGGGAGTGGTGGCTCACACCTGTAATCCCAGCATTTTGGGAAGCCGAGGC ACTATTATTTTAGGCCGGGAGTGGTGGCTCAC_CCTGTAATCCCAGCATTTTGGGAAGCCGAGGC GT G RAD1 Ensembl:ENSG00000113456 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1411192343 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_250658,Human_RBP_ID_17575385,Human_RBP_ID_27739981 11198 RMVar_ID_11198 Human_SNP_ID_227618677 A-to-I Human chr5 - 34906413 34906413 34906413 GCTAATCTTGAACTCCTGAGCTCAAGCAATCCACCCGCCTCGGCCTCCCAAAGGGCTGGGATTAC GCTAATCTTGAACTCCTGAGCTCAAGCAATCCCCCCGCCTCGGCCTCCCAAAGGGCTGGGATTAC T G RAD1 Ensembl:ENSG00000113456 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984673746 Functional Loss SNV dbSNP153 33..33 33 - - - 11199 RMVar_ID_11199 Human_SNP_ID_227618678 A-to-I Human chr5 - 34906417 34906417 34906417 CTAGGCTAATCTTGAACTCCTGAGCTCAAGCAATCCACCCGCCTCGGCCTCCCAAAGGGCTGGGA CTAGGCTAATCTTGAACTCCTGAGCTCAAGCAGTCCACCCGCCTCGGCCTCCCAAAGGGCTGGGA T C RAD1 Ensembl:ENSG00000113456 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs918955148 Functional Loss SNV dbSNP153 33..33 33 - - - 11200 RMVar_ID_11200 Human_SNP_ID_227618691 A-to-I Human chr5 - 34906456 34906456 34906456 TTTTGTATTTTTTGTAGAGATGGGGTTTTACTATGTTCCCTAGGCTAATCTTGAACTCCTGAGCT TTTTGTATTTTTTGTAGAGATGGGGTTTTACTGTGTTCCCTAGGCTAATCTTGAACTCCTGAGCT T C RAD1 Ensembl:ENSG00000113456 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917852663 Functional Loss SNV dbSNP153 33..33 33 - - - 11201 RMVar_ID_11201 Human_SNP_ID_227618695 A-to-I Human chr5 - 34906491 34906491 34906491 ACGACTACAGGTGCATGCCTCCATGCCCTGCTAATTTTTGTATTTTTTGTAGAGATGGGGTTTTA ACGACTACAGGTGCATGCCTCCATGCCCTGCTGATTTTTGTATTTTTTGTAGAGATGGGGTTTTA T C RAD1 Ensembl:ENSG00000113456 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs945321998 Functional Loss SNV dbSNP153 33..33 33 - - - 11202 RMVar_ID_11202 Human_SNP_ID_227618704 A-to-I Human chr5 - 34906529 34906529 34906529 GCTCAAGCAATCCTCCCATCTCAGCTTCCCAAATAGCTACGACTACAGGTGCATGCCTCCATGCC GCTCAAGCAATCCTCCCATCTCAGCTTCCCAAGTAGCTACGACTACAGGTGCATGCCTCCATGCC T C RAD1 Ensembl:ENSG00000113456 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1266520182 Functional Loss SNV dbSNP153 33..33 33 - - - 11203 RMVar_ID_11203 Human_SNP_ID_227618705 A-to-I Human chr5 - 34906530 34906530 34906530 GGCTCAAGCAATCCTCCCATCTCAGCTTCCCAAATAGCTACGACTACAGGTGCATGCCTCCATGC GGCTCAAGCAATCCTCCCATCTCAGCTTCCCAGATAGCTACGACTACAGGTGCATGCCTCCATGC T C RAD1 Ensembl:ENSG00000113456 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559054658 Functional Loss SNV dbSNP153 33..33 33 - - - 11204 RMVar_ID_11204 Human_SNP_ID_227618708 A-to-I Human chr5 - 34906544 34906544 34906544 GCCTCAATCTCCTAGGCTCAAGCAATCCTCCCATCTCAGCTTCCCAAATAGCTACGACTACAGGT GCCTCAATCTCCTAGGCTCAAGCAATCCTCCCGTCTCAGCTTCCCAAATAGCTACGACTACAGGT T C RAD1 Ensembl:ENSG00000113456 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1309631723 Functional Loss SNV dbSNP153 33..33 33 - - - 11205 RMVar_ID_11205 Human_SNP_ID_227618709 A-to-I Human chr5 - 34906552 34906552 34906552 TCACTCCAGCCTCAATCTCCTAGGCTCAAGCAATCCTCCCATCTCAGCTTCCCAAATAGCTACGA TCACTCCAGCCTCAATCTCCTAGGCTCAAGCATTCCTCCCATCTCAGCTTCCCAAATAGCTACGA T A RAD1 Ensembl:ENSG00000113456 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE99789;GSE107867;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;ASD brains,cerebellum;ASD brains,frontal_cortex;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 23474544,24183664,29129909,29796672,30559470,30559470,31158229,31158229 RNA-Seq:(High) rs1054551792 Functional Loss SNV dbSNP153 33..33 33 - - - 11206 RMVar_ID_11206 Human_SNP_ID_227618710 A-to-I Human chr5 - 34906552 34906552 34906552 TCACTCCAGCCTCAATCTCCTAGGCTCAAGCAATCCTCCCATCTCAGCTTCCCAAATAGCTACGA TCACTCCAGCCTCAATCTCCTAGGCTCAAGCAGTCCTCCCATCTCAGCTTCCCAAATAGCTACGA T C RAD1 Ensembl:ENSG00000113456 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE99789;GSE107867;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;ASD brains,cerebellum;ASD brains,frontal_cortex;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 23474544,24183664,29129909,29796672,30559470,30559470,31158229,31158229 RNA-Seq:(High) rs1054551792 Functional Loss SNV dbSNP153 33..33 33 - - - 11207 RMVar_ID_11207 Human_SNP_ID_227618713 A-to-I Human chr5 - 34906582 34906582 34906582 CAGGCTGGAGTACAGTTGTAGGATTACAGTTCACTCCAGCCTCAATCTCCTAGGCTCAAGCAATC CAGGCTGGAGTACAGTTGTAGGATTACAGTTCGCTCCAGCCTCAATCTCCTAGGCTCAAGCAATC T C RAD1 Ensembl:ENSG00000113456 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1057238976 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18047474 11208 RMVar_ID_11208 Human_SNP_ID_227618721 A-to-I Human chr5 - 34906633 34906633 34906633 ATCTCAGTTTTTTTATTTTTATTTTTGGAGACAAGATCTTGCTCTGTTGCCCAGGCTGGAGTACA ATCTCAGTTTTTTTATTTTTATTTTTGGAGACCAGATCTTGCTCTGTTGCCCAGGCTGGAGTACA T G RAD1 Ensembl:ENSG00000113456 Protein coding 3'UTR GSE47997;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,31158229,31158229,31158229 RNA-Seq:(High) rs1379287759 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7503069,Human_RBP_ID_15433797 11209 RMVar_ID_11209 Human_SNP_ID_227619083 A-to-I Human chr5 - 34908311 34908311 34908311 AAATTAGCCGGACGTGGTGGCACATGCCTGTAATGCCAGCTACTCGGGAGGCTGAGGCAGGAGAA AAATTAGCCGGACGTGGTGGCACATGCCTGTATTGCCAGCTACTCGGGAGGCTGAGGCAGGAGAA T A RAD1 Ensembl:ENSG00000113456 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1478706392 Functional Loss SNV dbSNP153 33..33 33 - - - 11210 RMVar_ID_11210 Human_SNP_ID_227619105 A-to-I Human chr5 - 34908407 34908407 34908407 ACTTTGGGAAGCCGAGGTGGGCGGATCACCTGAGGTCAGGAGTTCGAGACCAGCCTGACCAACGT ACTTTGGGAAGCCGAGGTGGGCGGATCACCTGGGGTCAGGAGTTCGAGACCAGCCTGACCAACGT T C RAD1 Ensembl:ENSG00000113456 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs3177099 Functional Loss SNV dbSNP153 33..33 33 - - - 11211 RMVar_ID_11211 Human_SNP_ID_227619116 A-to-I Human chr5 - 34908430 34908430 34908430 GGTGTGGTGGCTTTAATCCCAGCACTTTGGGAAGCCGAGGTGGGCGGATCACCTGAGGTCAGGAG GGTGTGGTGGCTTTAATCCCAGCACTTTGGGAGGCCGAGGTGGGCGGATCACCTGAGGTCAGGAG T C RAD1 Ensembl:ENSG00000113456 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs11542449 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18047492 11212 RMVar_ID_11212 Human_SNP_ID_227620450 A-to-I Human chr5 - 34913999 34913999 34913999 TGCAGGGGCATGGTATGGTGGCTCACACCTGTATTTCCAGCTGCTCAGGAGACCGAGGCTGAAGC TGCAGGGGCATGGTATGGTGGCTCACACCTGTGTTTCCAGCTGCTCAGGAGACCGAGGCTGAAGC T C RAD1 Ensembl:ENSG00000113456 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs890692358 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_642192,Human_Splice_Rec_642193,Human_Splice_Rec_642204,Human_Splice_Rec_642205,Human_Splice_Rec_642208,Human_Splice_Rec_642212 RMVar_hsa_circ_72665 11213 RMVar_ID_11213 Human_SNP_ID_227623056 A-to-I Human chr5 + 34923354 34923354 34923354 CAGGCTGGACTGCAGTGGCACAATCTTGGCTCACTGCAACCTCCACCTCCCGGGTTCAAGCTTCT CAGGCTGGACTGCAGTGGCACAATCTTGGCTCTCTGCAACCTCCACCTCCCGGGTTCAAGCTTCT A T BRIX1 Ensembl:ENSG00000113460 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1323825307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15434140 11214 RMVar_ID_11214 Human_SNP_ID_227627881 A-to-I Human chr5 + 34941253 34941253 34941253 AGGGTCTCACTCTGTCACCAAGGCAGGAGTGCAGTGGCACAGTCATGACTCACCACAGCCTCGAC AGGGTCTCACTCTGTCACCAAGGCAGGAGTGCGGTGGCACAGTCATGACTCACCACAGCCTCGAC A G DNAJC21 Ensembl:ENSG00000168724 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1008511036 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5869,RMVar_hsa_circ_348384,RMVar_hsa_circ_368886,RMVar_hsa_circ_32007 11215 RMVar_ID_11215 Human_SNP_ID_227627887 A-to-I Human chr5 + 34941272 34941272 34941272 AAGGCAGGAGTGCAGTGGCACAGTCATGACTCACCACAGCCTCGACCTGTTGAACTCAGATGATC AAGGCAGGAGTGCAGTGGCACAGTCATGACTCGCCACAGCCTCGACCTGTTGAACTCAGATGATC A G DNAJC21 Ensembl:ENSG00000168724 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1473538841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15434332,Human_RBP_ID_26702495 RMVar_hsa_circ_5869,RMVar_hsa_circ_348384,RMVar_hsa_circ_368886,RMVar_hsa_circ_32007 11216 RMVar_ID_11216 Human_SNP_ID_227627931 A-to-I Human chr5 + 34941491 34941491 34941491 GTGTTCCACCTGCCTCAGCCTTTCAAAGTGCTAGGATTGCAAGCGTGAGCCACTGCATCCAGTTA GTGTTCCACCTGCCTCAGCCTTTCAAAGTGCTGGGATTGCAAGCGTGAGCCACTGCATCCAGTTA A G DNAJC21 Ensembl:ENSG00000168724 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1435967147 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5869,RMVar_hsa_circ_348384,RMVar_hsa_circ_368886,RMVar_hsa_circ_32007 11217 RMVar_ID_11217 Human_SNP_ID_227630663 A-to-I Human chr5 + 34951760 34951760 34951760 GTTGCACAGGGTGGTCTTGAACTCCTGACCTCATGATCTGCCCGCCTTGGCCTACCAAAGTGCTG GTTGCACAGGGTGGTCTTGAACTCCTGACCTCGTGATCTGCCCGCCTTGGCCTACCAAAGTGCTG A G DNAJC21 Ensembl:ENSG00000168724 Protein coding intron GSE38233;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,32596459,32596459 RNA-Seq:(High) rs946339716 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15434548,Human_RBP_ID_24104327 RMVar_hsa_circ_368886 11218 RMVar_ID_11218 Human_SNP_ID_227630719 A-to-I Human chr5 + 34951976 34951976 34951976 CAAGTGACTTCTTCACAGCTGCAGAATGGCAGAGCTAAGATAGATACATTATACCCAGCACCCTC CAAGTGACTTCTTCACAGCTGCAGAATGGCAGGGCTAAGATAGATACATTATACCCAGCACCCTC A G DNAJC21 Ensembl:ENSG00000168724 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs37438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_641565 GWAS_ID_989 RMVar_hsa_circ_368886 11219 RMVar_ID_11219 Human_SNP_ID_227630720 A-to-I Human chr5 + 34951976 34951976 34951976 CAAGTGACTTCTTCACAGCTGCAGAATGGCAGAGCTAAGATAGATACATTATACCCAGCACCCTC CAAGTGACTTCTTCACAGCTGCAGAATGGCAGTGCTAAGATAGATACATTATACCCAGCACCCTC A T DNAJC21 Ensembl:ENSG00000168724 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs37438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_641565 GWAS_ID_989 RMVar_hsa_circ_368886 11220 RMVar_ID_11220 Human_SNP_ID_227630964 A-to-I Human chr5 + 34952893 34952893 34952893 TAATGTTAGGCCAGGCAGGGTGGCTCACGCTTATATTCCCAGCACTTTGGAAAGCCAAGGCGGGT TAATGTTAGGCCAGGCAGGGTGGCTCACGCTTGTATTCCCAGCACTTTGGAAAGCCAAGGCGGGT A G DNAJC21 Ensembl:ENSG00000168724 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs77937484 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_368886 11221 RMVar_ID_11221 Human_SNP_ID_227630968 A-to-I Human chr5 + 34952901 34952901 34952901 GGCCAGGCAGGGTGGCTCACGCTTATATTCCCAGCACTTTGGAAAGCCAAGGCGGGTGGATCACG GGCCAGGCAGGGTGGCTCACGCTTATATTCCCGGCACTTTGGAAAGCCAAGGCGGGTGGATCACG A G DNAJC21 Ensembl:ENSG00000168724 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1201634797 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_368886 11222 RMVar_ID_11222 Human_SNP_ID_227631005 A-to-I Human chr5 + 34953039 34953039 34953039 GAGTATGGTGGCACGTGCCTGTAATCCCAGCTATTCGGGAGGCTGAAGCAGGAAAATCGCTTGAA GAGTATGGTGGCACGTGCCTGTAATCCCAGCTGTTCGGGAGGCTGAAGCAGGAAAATCGCTTGAA A G DNAJC21 Ensembl:ENSG00000168724 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971416347 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_368886 11223 RMVar_ID_11223 Human_SNP_ID_227631092 A-to-I Human chr5 + 34953348 34953348 34953348 CAGTGGTGCAATCTTGGCTCACTGCAGTCTCCACCTCCTGGGTTCAAGTGATTCCCCTGCTCCTC CAGTGGTGCAATCTTGGCTCACTGCAGTCTCCGCCTCCTGGGTTCAAGTGATTCCCCTGCTCCTC A G DNAJC21 Ensembl:ENSG00000168724 Protein coding intron GSE123020:GSM3490829,GSM3490830,GSM3490831 esophageal squamous carcinoma cells,EC109 cell line - 32596459 RNA-Seq:(High) rs951733271 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_368886 11224 RMVar_ID_11224 Human_SNP_ID_227631103 A-to-I Human chr5 + 34953400 34953400 34953400 TCCCCTGCTCCTCCTCCTAAGTAACTGGGATTACAGGTGCCTGCCACCACGCTCAGCTAATTTTT TCCCCTGCTCCTCCTCCTAAGTAACTGGGATTGCAGGTGCCTGCCACCACGCTCAGCTAATTTTT A G DNAJC21 Ensembl:ENSG00000168724 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1379229732 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_368886 11225 RMVar_ID_11225 Human_SNP_ID_227631122 A-to-I Human chr5 + 34953463 34953463 34953463 TTTATATTTTTAATAGAGGCGGAGGTTTCACCATGTTGGCCAAGCTGGTCTCGAGCTCCTGACCT TTTATATTTTTAATAGAGGCGGAGGTTTCACCGTGTTGGCCAAGCTGGTCTCGAGCTCCTGACCT A G DNAJC21 Ensembl:ENSG00000168724 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs974173880 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_368886 11226 RMVar_ID_11226 Human_SNP_ID_227922123 A-to-I Human chr5 - 36146510 36146510 36146510 TTAAAATTAGCCAGGCGTGGTGGTGTGCACCTATAGTCCTAGCTATCTGGAAGCTGAGGTGGGAG TTAAAATTAGCCAGGCGTGGTGGTGTGCACCTGTAGTCCTAGCTATCTGGAAGCTGAGGTGGGAG T C LMBRD2 Ensembl:ENSG00000164187 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs757290278 Functional Loss SNV dbSNP153 33..33 33 - - - 11227 RMVar_ID_11227 Human_SNP_ID_227933350 A-to-I Human chr5 - 36194043 36194043 36194043 TCTACTTATAAGTAATCCTAGAATTTTTGCCAAAAGATCCTGTCGTTGCATAATCAAACAGTTGG TCTACTTATAAGTAATCCTAGAATTTTTGCCAGAAGATCCTGTCGTTGCATAATCAAACAGTTGG T C NADK2 Ensembl:ENSG00000152620 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs544430008 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_641793,Human_RBP_ID_2927523,Human_RBP_ID_8214335,Human_RBP_ID_15435799,Human_RBP_ID_17302646,Human_RBP_ID_24506490 Human_miRNA_ID_140632,Human_miRNA_ID_417643 11228 RMVar_ID_11228 Human_SNP_ID_227933351 A-to-I Human chr5 - 36194043 36194043 36194043 TCTACTTATAAGTAATCCTAGAATTTTTGCCAAAAGATCCTGTCGTTGCATAATCAAACAGTTGG TCTACTTATAAGTAATCCTAGAATTTTTGCCACAAGATCCTGTCGTTGCATAATCAAACAGTTGG T G NADK2 Ensembl:ENSG00000152620 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs544430008 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_641793,Human_RBP_ID_2927523,Human_RBP_ID_8214335,Human_RBP_ID_15435799,Human_RBP_ID_17302646,Human_RBP_ID_24506490 Human_miRNA_ID_140632,Human_miRNA_ID_417643 11229 RMVar_ID_11229 Human_SNP_ID_227939414 A-to-I Human chr5 - 36221275 36221275 36221275 AGGCTTGACTTGGGCTGGAGGATCCACTTTCAAGATGGCCCACTCACATGGACTCATCTAAATCA AGGCTTGACTTGGGCTGGAGGATCCACTTTCAGGATGGCCCACTCACATGGACTCATCTAAATCA T C NADK2 Ensembl:ENSG00000152620 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971474125 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_46379,RMVar_hsa_circ_54357,RMVar_hsa_circ_230821,RMVar_hsa_circ_230819,RMVar_hsa_circ_275054,RMVar_hsa_circ_281702,RMVar_hsa_circ_230822,RMVar_hsa_circ_318004,RMVar_hsa_circ_358365 11230 RMVar_ID_11230 Human_SNP_ID_228043605 A-to-I Human chr5 + 36645465 36645465 36645465 TCTCTTCCCCAGCTGCCCAAGTAGCTGGAATTACAGGTGCCTACCACCACGCCCAGTTAATTTTT TCTCTTCCCCAGCTGCCCAAGTAGCTGGAATTGCAGGTGCCTACCACCACGCCCAGTTAATTTTT A G SLC1A3 Ensembl:ENSG00000079215 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs555135369 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_230824,RMVar_hsa_circ_87918 11231 RMVar_ID_11231 Human_SNP_ID_228043634 A-to-I Human chr5 + 36645599 36645599 36645599 CCCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGATGTGAGCCACCGCGCCCGGCCCTCCATT CCCCCACCTCGGCCTCCCAAAGTGCTGGGATTGCAGATGTGAGCCACCGCGCCCGGCCCTCCATT A G SLC1A3 Ensembl:ENSG00000079215 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1028586603 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_230824,RMVar_hsa_circ_87918 11232 RMVar_ID_11232 Human_SNP_ID_228106772 A-to-I Human chr5 + 36923033 36923033 36923033 CTTCTAGGCCAGGGCTGGTGGCTCACACCTGTAATCCCAGAACTTTGGGAGGCCGAGGCGGGCGG CTTCTAGGCCAGGGCTGGTGGCTCACACCTGTGATCCCAGAACTTTGGGAGGCCGAGGCGGGCGG A G NIPBL Ensembl:ENSG00000164190 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992992274 Functional Loss SNV dbSNP153 33..33 33 - - - 11233 RMVar_ID_11233 Human_SNP_ID_228118257 A-to-I Human chr5 + 36968735 36968735 36968735 AAAAAGGAGAAGAGGTTGATTTAATGTTACCTAGTGGTAGAAAAAATTAGAAACATTTTGTTTCA AAAAAGGAGAAGAGGTTGATTTAATGTTACCTGGTGGTAGAAAAAATTAGAAACATTTTGTTTCA A G NIPBL Ensembl:ENSG00000164190 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs573630450 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83963,RMVar_hsa_circ_118831,RMVar_hsa_circ_363179,RMVar_hsa_circ_292378,RMVar_hsa_circ_282135,RMVar_hsa_circ_274782,RMVar_hsa_circ_121686,RMVar_hsa_circ_96902,RMVar_hsa_circ_113306,RMVar_hsa_circ_116217,RMVar_hsa_circ_106642,RMVar_hsa_circ_91282,RMVar_hsa_circ_96476,RMVar_hsa_circ_84594,RMVar_hsa_circ_230830,RMVar_hsa_circ_230834,RMVar_hsa_circ_230838,RMVar_hsa_circ_230842,RMVar_hsa_circ_230840,RMVar_hsa_circ_230841,RMVar_hsa_circ_230839,RMVar_hsa_circ_230836,RMVar_hsa_circ_230837,RMVar_hsa_circ_230835,RMVar_hsa_circ_230832,RMVar_hsa_circ_230833,RMVar_hsa_circ_230831,RMVar_hsa_circ_49844,RMVar_hsa_circ_332981,RMVar_hsa_circ_83407,RMVar_hsa_circ_10000,RMVar_hsa_circ_45425,RMVar_hsa_circ_86101,RMVar_hsa_circ_230848,RMVar_hsa_circ_102251,RMVar_hsa_circ_16093,RMVar_hsa_circ_230852,RMVar_hsa_circ_81153,RMVar_hsa_circ_230849,RMVar_hsa_circ_230850,RMVar_hsa_circ_81509,RMVar_hsa_circ_359160,RMVar_hsa_circ_230853,RMVar_hsa_circ_230851 11234 RMVar_ID_11234 Human_SNP_ID_228123457 A-to-I Human chr5 + 36989707 36989707 36989707 TAAAAATACAAAAATTAGTTAGGCACTGTGGCAGGCACTTGGTAGCCCCAGCTACTCAGGAGGCT TAAAAATACAAAAATTAGTTAGGCACTGTGGCGGGCACTTGGTAGCCCCAGCTACTCAGGAGGCT A G NIPBL Ensembl:ENSG00000164190 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs777993905 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7435196,Human_RBP_ID_15439768 RMVar_hsa_circ_83963,RMVar_hsa_circ_118831,RMVar_hsa_circ_363179,RMVar_hsa_circ_121686,RMVar_hsa_circ_96902,RMVar_hsa_circ_113306,RMVar_hsa_circ_116217,RMVar_hsa_circ_106642,RMVar_hsa_circ_91282,RMVar_hsa_circ_96476,RMVar_hsa_circ_84594,RMVar_hsa_circ_2823,RMVar_hsa_circ_230830,RMVar_hsa_circ_230834,RMVar_hsa_circ_230838,RMVar_hsa_circ_230839,RMVar_hsa_circ_230836,RMVar_hsa_circ_230837,RMVar_hsa_circ_230835,RMVar_hsa_circ_230832,RMVar_hsa_circ_230833,RMVar_hsa_circ_230831,RMVar_hsa_circ_83407,RMVar_hsa_circ_10000,RMVar_hsa_circ_86101,RMVar_hsa_circ_230848,RMVar_hsa_circ_102251,RMVar_hsa_circ_230852,RMVar_hsa_circ_81153,RMVar_hsa_circ_230849,RMVar_hsa_circ_230850,RMVar_hsa_circ_81509,RMVar_hsa_circ_230853,RMVar_hsa_circ_55053,RMVar_hsa_circ_7839,RMVar_hsa_circ_17727,RMVar_hsa_circ_2182,RMVar_hsa_circ_123214,RMVar_hsa_circ_335398,RMVar_hsa_circ_230854,RMVar_hsa_circ_230855,RMVar_hsa_circ_267499,RMVar_hsa_circ_269536,RMVar_hsa_circ_355849,RMVar_hsa_circ_359712,RMVar_hsa_circ_124681,RMVar_hsa_circ_125743,RMVar_hsa_circ_60831,RMVar_hsa_circ_230859,RMVar_hsa_circ_230860 11235 RMVar_ID_11235 Human_SNP_ID_228128644 A-to-I Human chr5 + 37011354 37011354 37011354 AAGGTGGGCAGATTGCTTGAGGCCAGGAGTTCAAGACCAGTTGGGCAACATGACAAAACTCTGTC AAGGTGGGCAGATTGCTTGAGGCCAGGAGTTCGAGACCAGTTGGGCAACATGACAAAACTCTGTC A G NIPBL Ensembl:ENSG00000164190 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs916395647 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83963,RMVar_hsa_circ_113306,RMVar_hsa_circ_116217,RMVar_hsa_circ_106642,RMVar_hsa_circ_96476,RMVar_hsa_circ_84594,RMVar_hsa_circ_2823,RMVar_hsa_circ_230830,RMVar_hsa_circ_230834,RMVar_hsa_circ_230835,RMVar_hsa_circ_230832,RMVar_hsa_circ_230833,RMVar_hsa_circ_230831,RMVar_hsa_circ_86101,RMVar_hsa_circ_102251,RMVar_hsa_circ_81153,RMVar_hsa_circ_230849,RMVar_hsa_circ_230850,RMVar_hsa_circ_230853,RMVar_hsa_circ_5570,RMVar_hsa_circ_267499,RMVar_hsa_circ_269536,RMVar_hsa_circ_124681,RMVar_hsa_circ_125743,RMVar_hsa_circ_60831,RMVar_hsa_circ_230859,RMVar_hsa_circ_230860,RMVar_hsa_circ_363338,RMVar_hsa_circ_374568,RMVar_hsa_circ_34485,RMVar_hsa_circ_117459,RMVar_hsa_circ_39442,RMVar_hsa_circ_322761,RMVar_hsa_circ_230861,RMVar_hsa_circ_364387,RMVar_hsa_circ_31810,RMVar_hsa_circ_353198,RMVar_hsa_circ_230863,RMVar_hsa_circ_343840,RMVar_hsa_circ_332680,RMVar_hsa_circ_37075,RMVar_hsa_circ_21867,RMVar_hsa_circ_33350,RMVar_hsa_circ_18699,RMVar_hsa_circ_94873,RMVar_hsa_circ_55588,RMVar_hsa_circ_75301,RMVar_hsa_circ_230865,RMVar_hsa_circ_5116,RMVar_hsa_circ_67608,RMVar_hsa_circ_24724,RMVar_hsa_circ_112701,RMVar_hsa_circ_230867,RMVar_hsa_circ_230868 11236 RMVar_ID_11236 Human_SNP_ID_228130070 A-to-I Human chr5 + 37015552 37015552 37015552 GTCAGTTCGAGACCAGCCTGACCAGCGTGGTGAAACCCTGTCTCTACTAAAAATACAAAAATTAG GTCAGTTCGAGACCAGCCTGACCAGCGTGGTGCAACCCTGTCTCTACTAAAAATACAAAAATTAG A C NIPBL Ensembl:ENSG00000164190 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs937344424 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83963,RMVar_hsa_circ_113306,RMVar_hsa_circ_116217,RMVar_hsa_circ_106642,RMVar_hsa_circ_96476,RMVar_hsa_circ_84594,RMVar_hsa_circ_2823,RMVar_hsa_circ_230830,RMVar_hsa_circ_230834,RMVar_hsa_circ_230835,RMVar_hsa_circ_230832,RMVar_hsa_circ_230833,RMVar_hsa_circ_230831,RMVar_hsa_circ_86101,RMVar_hsa_circ_102251,RMVar_hsa_circ_81153,RMVar_hsa_circ_230849,RMVar_hsa_circ_230850,RMVar_hsa_circ_230853,RMVar_hsa_circ_5570,RMVar_hsa_circ_267499,RMVar_hsa_circ_269536,RMVar_hsa_circ_124681,RMVar_hsa_circ_125743,RMVar_hsa_circ_60831,RMVar_hsa_circ_230859,RMVar_hsa_circ_230860,RMVar_hsa_circ_363338,RMVar_hsa_circ_374568,RMVar_hsa_circ_34485,RMVar_hsa_circ_117459,RMVar_hsa_circ_39442,RMVar_hsa_circ_322761,RMVar_hsa_circ_230861,RMVar_hsa_circ_364387,RMVar_hsa_circ_31810,RMVar_hsa_circ_353198,RMVar_hsa_circ_230863,RMVar_hsa_circ_343840,RMVar_hsa_circ_332680,RMVar_hsa_circ_37075,RMVar_hsa_circ_21867,RMVar_hsa_circ_33350,RMVar_hsa_circ_18699,RMVar_hsa_circ_94873,RMVar_hsa_circ_55588,RMVar_hsa_circ_75301,RMVar_hsa_circ_230865,RMVar_hsa_circ_5116,RMVar_hsa_circ_67608,RMVar_hsa_circ_24724,RMVar_hsa_circ_18076,RMVar_hsa_circ_112701,RMVar_hsa_circ_230867,RMVar_hsa_circ_267508,RMVar_hsa_circ_373721,RMVar_hsa_circ_230868,RMVar_hsa_circ_373269,RMVar_hsa_circ_104021,RMVar_hsa_circ_230869,RMVar_hsa_circ_230871,RMVar_hsa_circ_15792,RMVar_hsa_circ_230870 11237 RMVar_ID_11237 Human_SNP_ID_228130071 A-to-I Human chr5 + 37015552 37015552 37015552 GTCAGTTCGAGACCAGCCTGACCAGCGTGGTGAAACCCTGTCTCTACTAAAAATACAAAAATTAG GTCAGTTCGAGACCAGCCTGACCAGCGTGGTGTAACCCTGTCTCTACTAAAAATACAAAAATTAG A T NIPBL Ensembl:ENSG00000164190 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs937344424 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83963,RMVar_hsa_circ_113306,RMVar_hsa_circ_116217,RMVar_hsa_circ_106642,RMVar_hsa_circ_96476,RMVar_hsa_circ_84594,RMVar_hsa_circ_2823,RMVar_hsa_circ_230830,RMVar_hsa_circ_230834,RMVar_hsa_circ_230835,RMVar_hsa_circ_230832,RMVar_hsa_circ_230833,RMVar_hsa_circ_230831,RMVar_hsa_circ_86101,RMVar_hsa_circ_102251,RMVar_hsa_circ_81153,RMVar_hsa_circ_230849,RMVar_hsa_circ_230850,RMVar_hsa_circ_230853,RMVar_hsa_circ_5570,RMVar_hsa_circ_267499,RMVar_hsa_circ_269536,RMVar_hsa_circ_124681,RMVar_hsa_circ_125743,RMVar_hsa_circ_60831,RMVar_hsa_circ_230859,RMVar_hsa_circ_230860,RMVar_hsa_circ_363338,RMVar_hsa_circ_374568,RMVar_hsa_circ_34485,RMVar_hsa_circ_117459,RMVar_hsa_circ_39442,RMVar_hsa_circ_322761,RMVar_hsa_circ_230861,RMVar_hsa_circ_364387,RMVar_hsa_circ_31810,RMVar_hsa_circ_353198,RMVar_hsa_circ_230863,RMVar_hsa_circ_343840,RMVar_hsa_circ_332680,RMVar_hsa_circ_37075,RMVar_hsa_circ_21867,RMVar_hsa_circ_33350,RMVar_hsa_circ_18699,RMVar_hsa_circ_94873,RMVar_hsa_circ_55588,RMVar_hsa_circ_75301,RMVar_hsa_circ_230865,RMVar_hsa_circ_5116,RMVar_hsa_circ_67608,RMVar_hsa_circ_24724,RMVar_hsa_circ_18076,RMVar_hsa_circ_112701,RMVar_hsa_circ_230867,RMVar_hsa_circ_267508,RMVar_hsa_circ_373721,RMVar_hsa_circ_230868,RMVar_hsa_circ_373269,RMVar_hsa_circ_104021,RMVar_hsa_circ_230869,RMVar_hsa_circ_230871,RMVar_hsa_circ_15792,RMVar_hsa_circ_230870 11238 RMVar_ID_11238 Human_SNP_ID_228130072 A-to-I Human chr5 + 37015553 37015553 37015553 TCAGTTCGAGACCAGCCTGACCAGCGTGGTGAAACCCTGTCTCTACTAAAAATACAAAAATTAGC TCAGTTCGAGACCAGCCTGACCAGCGTGGTGACACCCTGTCTCTACTAAAAATACAAAAATTAGC A C NIPBL Ensembl:ENSG00000164190 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs895752597 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83963,RMVar_hsa_circ_113306,RMVar_hsa_circ_116217,RMVar_hsa_circ_106642,RMVar_hsa_circ_96476,RMVar_hsa_circ_84594,RMVar_hsa_circ_2823,RMVar_hsa_circ_230830,RMVar_hsa_circ_230834,RMVar_hsa_circ_230835,RMVar_hsa_circ_230832,RMVar_hsa_circ_230833,RMVar_hsa_circ_230831,RMVar_hsa_circ_86101,RMVar_hsa_circ_102251,RMVar_hsa_circ_81153,RMVar_hsa_circ_230849,RMVar_hsa_circ_230850,RMVar_hsa_circ_230853,RMVar_hsa_circ_5570,RMVar_hsa_circ_267499,RMVar_hsa_circ_269536,RMVar_hsa_circ_124681,RMVar_hsa_circ_125743,RMVar_hsa_circ_60831,RMVar_hsa_circ_230859,RMVar_hsa_circ_230860,RMVar_hsa_circ_363338,RMVar_hsa_circ_374568,RMVar_hsa_circ_34485,RMVar_hsa_circ_117459,RMVar_hsa_circ_39442,RMVar_hsa_circ_322761,RMVar_hsa_circ_230861,RMVar_hsa_circ_364387,RMVar_hsa_circ_31810,RMVar_hsa_circ_353198,RMVar_hsa_circ_230863,RMVar_hsa_circ_343840,RMVar_hsa_circ_332680,RMVar_hsa_circ_37075,RMVar_hsa_circ_21867,RMVar_hsa_circ_33350,RMVar_hsa_circ_18699,RMVar_hsa_circ_94873,RMVar_hsa_circ_55588,RMVar_hsa_circ_75301,RMVar_hsa_circ_230865,RMVar_hsa_circ_5116,RMVar_hsa_circ_67608,RMVar_hsa_circ_24724,RMVar_hsa_circ_18076,RMVar_hsa_circ_112701,RMVar_hsa_circ_230867,RMVar_hsa_circ_267508,RMVar_hsa_circ_373721,RMVar_hsa_circ_230868,RMVar_hsa_circ_373269,RMVar_hsa_circ_104021,RMVar_hsa_circ_230869,RMVar_hsa_circ_230871,RMVar_hsa_circ_15792,RMVar_hsa_circ_230870 11239 RMVar_ID_11239 Human_SNP_ID_228139537 A-to-I Human chr5 + 37050955 37050955 37050955 GGATTCAAGCACTCTTCCCACCTCTGCCTCCCAAGTAGCTGAGACTACAGGTGTGCGCCACCACC GGATTCAAGCACTCTTCCCACCTCTGCCTCCCCAGTAGCTGAGACTACAGGTGTGCGCCACCACC A C NIPBL Ensembl:ENSG00000164190 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982704379 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_787,RMVar_hsa_circ_83963,RMVar_hsa_circ_106642,RMVar_hsa_circ_96476,RMVar_hsa_circ_230830,RMVar_hsa_circ_230832,RMVar_hsa_circ_230831,RMVar_hsa_circ_124681,RMVar_hsa_circ_230860,RMVar_hsa_circ_322761,RMVar_hsa_circ_332680,RMVar_hsa_circ_10752,RMVar_hsa_circ_75301,RMVar_hsa_circ_267508,RMVar_hsa_circ_62611,RMVar_hsa_circ_75445,RMVar_hsa_circ_367942,RMVar_hsa_circ_8230,RMVar_hsa_circ_117341,RMVar_hsa_circ_21401,RMVar_hsa_circ_230878,RMVar_hsa_circ_11001,RMVar_hsa_circ_230882,RMVar_hsa_circ_89135,RMVar_hsa_circ_230884 11240 RMVar_ID_11240 Human_SNP_ID_228139555 A-to-I Human chr5 + 37051024 37051024 37051024 TAATTTTTGTGTTTTTGTAGAGACGGGGTTTTACCATGTTGGCCAGGCTGGTCTCAAACTTCTGA TAATTTTTGTGTTTTTGTAGAGACGGGGTTTTGCCATGTTGGCCAGGCTGGTCTCAAACTTCTGA A G NIPBL Ensembl:ENSG00000164190 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1013729662 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_787,RMVar_hsa_circ_83963,RMVar_hsa_circ_106642,RMVar_hsa_circ_96476,RMVar_hsa_circ_230830,RMVar_hsa_circ_230832,RMVar_hsa_circ_230831,RMVar_hsa_circ_124681,RMVar_hsa_circ_230860,RMVar_hsa_circ_322761,RMVar_hsa_circ_332680,RMVar_hsa_circ_10752,RMVar_hsa_circ_75301,RMVar_hsa_circ_267508,RMVar_hsa_circ_62611,RMVar_hsa_circ_75445,RMVar_hsa_circ_367942,RMVar_hsa_circ_8230,RMVar_hsa_circ_117341,RMVar_hsa_circ_21401,RMVar_hsa_circ_230878,RMVar_hsa_circ_11001,RMVar_hsa_circ_230882,RMVar_hsa_circ_89135,RMVar_hsa_circ_230884 11241 RMVar_ID_11241 Human_SNP_ID_228139558 A-to-I Human chr5 + 37051047 37051047 37051047 CGGGGTTTTACCATGTTGGCCAGGCTGGTCTCAAACTTCTGAGCTCAAGTAATCTGCCTGCCTCA CGGGGTTTTACCATGTTGGCCAGGCTGGTCTCGAACTTCTGAGCTCAAGTAATCTGCCTGCCTCA A G NIPBL Ensembl:ENSG00000164190 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1325448184 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_787,RMVar_hsa_circ_83963,RMVar_hsa_circ_106642,RMVar_hsa_circ_96476,RMVar_hsa_circ_230830,RMVar_hsa_circ_230832,RMVar_hsa_circ_230831,RMVar_hsa_circ_124681,RMVar_hsa_circ_230860,RMVar_hsa_circ_322761,RMVar_hsa_circ_332680,RMVar_hsa_circ_10752,RMVar_hsa_circ_75301,RMVar_hsa_circ_267508,RMVar_hsa_circ_62611,RMVar_hsa_circ_75445,RMVar_hsa_circ_367942,RMVar_hsa_circ_8230,RMVar_hsa_circ_117341,RMVar_hsa_circ_21401,RMVar_hsa_circ_230878,RMVar_hsa_circ_11001,RMVar_hsa_circ_230882,RMVar_hsa_circ_89135,RMVar_hsa_circ_230884 11242 RMVar_ID_11242 Human_SNP_ID_228145365 A-to-I Human chr5 - 37074786 37074786 37074786 AACAATAGAGATGGGATCTTGCTTTGTTGTCCAGGCTGGTTTTGAACTCTTGGCTTCAAGCAATC AACAATAGAGATGGGATCTTGCTTTGTTGTCCTGGCTGGTTTTGAACTCTTGGCTTCAAGCAATC T A lnc-BBS5-6 RNACentral:URS0000E2127A lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1399988852 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18842220 11243 RMVar_ID_11243 Human_SNP_ID_228146224 A-to-I Human chr5 - 37077867 37077867 37077867 TTACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGAGGATCGCTTGAGTCCAGGAGATCA TTACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGAGGATCGCTTGAGTCCAGGAGATCA T C lnc-BBS5-6 RNACentral:URS0000E2127A lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1440202396 Functional Loss SNV dbSNP153 33..33 33 - - - 11244 RMVar_ID_11244 Human_SNP_ID_228151685 A-to-I Human chr5 - 37102311 37102311 37102311 TGATGGTGCAAGCCTGTAATCCTAGCTACTTGAGAGTCTGAGGCAGGAGAATTGCTTGAACCTGC TGATGGTGCAAGCCTGTAATCCTAGCTACTTGGGAGTCTGAGGCAGGAGAATTGCTTGAACCTGC T C lnc-BBS5-6 RNACentral:URS0000E2127A lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1371379067 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2929332,Human_RBP_ID_25893172 11245 RMVar_ID_11245 Human_SNP_ID_228152315 A-to-I Human chr5 - 37105286 37105286 37105286 TTGTTTTTGTCTTTGTTTTGAGACAGGATCTCACTTTGTTCTCCAGGCTGGAATGCAGTGGTGTG TTGTTTTTGTCTTTGTTTTGAGACAGGATCTCTCTTTGTTCTCCAGGCTGGAATGCAGTGGTGTG T A lnc-BBS5-6 RNACentral:URS0000E2127A lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs970719354 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15440768 11246 RMVar_ID_11246 Human_SNP_ID_228152414 A-to-I Human chr5 - 37105778 37105778 37105778 TTGTTTGAGTTCTTTATATATTGCGGTTATTAATCCTTTGCTGGATGGGTAGCTTGCAAATATTT TTGTTTGAGTTCTTTATATATTGCGGTTATTAGTCCTTTGCTGGATGGGTAGCTTGCAAATATTT T C lnc-BBS5-6 RNACentral:URS0000E2127A lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs192942231 Functional Loss SNV dbSNP153 33..33 33 - - - 11247 RMVar_ID_11247 Human_SNP_ID_228157187 A-to-I Human chr5 - 37126163 37126163 37126163 ACAGTCACTGCTCACTGCAGCTTCGACCTCCCAGGCTCAAGTGATCCTCCCACCCACCTCAGCAT ACAGTCACTGCTCACTGCAGCTTCGACCTCCCGGGCTCAAGTGATCCTCCCACCCACCTCAGCAT T C CPLANE1 Ensembl:ENSG00000197603 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1451283070 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_86526,RMVar_hsa_circ_313599,RMVar_hsa_circ_230901,RMVar_hsa_circ_230903,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_350747,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_230905,RMVar_hsa_circ_230906 11248 RMVar_ID_11248 Human_SNP_ID_228180514 A-to-I Human chr5 - 37225770 37225770 37225770 CGGCTCACTGCAACCTCCGCCTCCTGGGTTCAAGTAGATTCTCCTGCCTCAGCCCCCCGAGTAGC CGGCTCACTGCAACCTCCGCCTCCTGGGTTCAGGTAGATTCTCCTGCCTCAGCCCCCCGAGTAGC T C CPLANE1 Ensembl:ENSG00000197603 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971394801 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_313599,RMVar_hsa_circ_37191,RMVar_hsa_circ_19407,RMVar_hsa_circ_36271,RMVar_hsa_circ_230922,RMVar_hsa_circ_86106,RMVar_hsa_circ_230924,RMVar_hsa_circ_230925,RMVar_hsa_circ_38346,RMVar_hsa_circ_36226,RMVar_hsa_circ_304351,RMVar_hsa_circ_28047,RMVar_hsa_circ_26337,RMVar_hsa_circ_230927,RMVar_hsa_circ_319381,RMVar_hsa_circ_230937,RMVar_hsa_circ_284218,RMVar_hsa_circ_230943,RMVar_hsa_circ_12287,RMVar_hsa_circ_230941,RMVar_hsa_circ_230942,RMVar_hsa_circ_338561,RMVar_hsa_circ_49570,RMVar_hsa_circ_25476,RMVar_hsa_circ_294837,RMVar_hsa_circ_72202,RMVar_hsa_circ_230948,RMVar_hsa_circ_368892,RMVar_hsa_circ_358673,RMVar_hsa_circ_14931,RMVar_hsa_circ_25205,RMVar_hsa_circ_7419,RMVar_hsa_circ_230951,RMVar_hsa_circ_299392,RMVar_hsa_circ_329552,RMVar_hsa_circ_9439,RMVar_hsa_circ_230955,RMVar_hsa_circ_121079,RMVar_hsa_circ_299610,RMVar_hsa_circ_367574,RMVar_hsa_circ_305018,RMVar_hsa_circ_15217,RMVar_hsa_circ_78199,RMVar_hsa_circ_230956,RMVar_hsa_circ_230958,RMVar_hsa_circ_230960,RMVar_hsa_circ_230959,RMVar_hsa_circ_230957,RMVar_hsa_circ_43666,RMVar_hsa_circ_298819,RMVar_hsa_circ_328318,RMVar_hsa_circ_357508,RMVar_hsa_circ_326538,RMVar_hsa_circ_230966,RMVar_hsa_circ_230967,RMVar_hsa_circ_230965,RMVar_hsa_circ_35650,RMVar_hsa_circ_105606,RMVar_hsa_circ_109039,RMVar_hsa_circ_230968,RMVar_hsa_circ_230969,RMVar_hsa_circ_230970 11249 RMVar_ID_11249 Human_SNP_ID_228192985 A-to-I Human chr5 + 37277139 37277139 37277139 CACCACCGCGCCCAGCCAATTTTTGTATTCTTAGTAGAGACAGGGTTTCACCATGTTGGCCGGGC CACCACCGCGCCCAGCCAATTTTTGTATTCTTGGTAGAGACAGGGTTTCACCATGTTGGCCGGGC A G RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs568021880 Functional Loss SNV dbSNP153 33..33 33 - - - 11250 RMVar_ID_11250 Human_SNP_ID_228195451 A-to-I Human chr5 - 37286957 37286957 37286957 CGGAGGTTGTGGTTAGCCAAGATCGCGCCACTACATTCCAGCCTGGGCAACAAGAGCGAAACTCC CGGAGGTTGTGGTTAGCCAAGATCGCGCCACTGCATTCCAGCCTGGGCAACAAGAGCGAAACTCC T C AC025449.1 Ensembl:ENSG00000270558 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1418158663 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15441442,Human_RBP_ID_25941387 11251 RMVar_ID_11251 Human_SNP_ID_228195487 A-to-I Human chr5 - 37287104 37287104 37287104 GAGGTTGGGAGATCGAGACCAGTCTGATCAACATGGAGAAACCCTGTTTCTACTAAAAATACGAA GAGGTTGGGAGATCGAGACCAGTCTGATCAACGTGGAGAAACCCTGTTTCTACTAAAAATACGAA T C lnc-BBS5-6 RNACentral:URS0000E2127A lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs938242309 Functional Loss SNV dbSNP153 33..33 33 - - - 11252 RMVar_ID_11252 Human_SNP_ID_228195490 A-to-I Human chr5 - 37287127 37287121 37287128 AGGCCGAGGCAGGCAGATCACCTGAGGTTGGGAGATCGAGACCAGTCTGATCAACATGGAGAAAC AGGCCGAGGCAGGCAGATCACCTGAGGTTGG_______AGACCAGTCTGATCAACATGGAGAAAC TCGATCTC T lnc-BBS5-6 RNACentral:URS0000E2127A lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202462665 Functional Loss DEL dbSNP153 32..38 33 - - - 11253 RMVar_ID_11253 Human_SNP_ID_228195513 A-to-I Human chr5 - 37287192 37287192 37287192 AACAATAGAATAAAAAAGTTGGGGCCGGGCACAGTGGCTTACGCCTGTAATCCCAGCACTTTGGG AACAATAGAATAAAAAAGTTGGGGCCGGGCACGGTGGCTTACGCCTGTAATCCCAGCACTTTGGG T C lnc-BBS5-6 RNACentral:URS0000E2127A lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984281538 Functional Loss SNV dbSNP153 33..33 33 - - - 11254 RMVar_ID_11254 Human_SNP_ID_228195663 A-to-I Human chr5 - 37287835 37287835 37287835 CCAGCTACTTGGGAGGCTGAGGCATGAGAATCACTTGAACCTTGGAGACAGAGGTGCAGTGAGCT CCAGCTACTTGGGAGGCTGAGGCATGAGAATCCCTTGAACCTTGGAGACAGAGGTGCAGTGAGCT T G lnc-BBS5-6 RNACentral:URS0000E2127A lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1561758663 Functional Loss SNV dbSNP153 33..33 33 - - - 11255 RMVar_ID_11255 Human_SNP_ID_228195864 A-to-I Human chr5 - 37288665 37288665 37288665 AAACTCCTGGCCTTAAGTGATTCCCCTGCCTCAGTCTCCCAAAGTGCTGGGATTATAGGCATGAG AAACTCCTGGCCTTAAGTGATTCCCCTGCCTCGGTCTCCCAAAGTGCTGGGATTATAGGCATGAG T C NUP155 Ensembl:ENSG00000113569 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1020566098 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23193563,Human_RBP_ID_24105408 11256 RMVar_ID_11256 Human_SNP_ID_228196016 A-to-I Human chr5 - 37288988 37288988 37288988 TGGCTCACCACAACCTCCACTTCCTGGGTTCAAGCAATTCTTCTGCCTCAGCCTCCCGAGTAGCT TGGCTCACCACAACCTCCACTTCCTGGGTTCAGGCAATTCTTCTGCCTCAGCCTCCCGAGTAGCT T C NUP155 Ensembl:ENSG00000113569 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs990696010 Functional Loss SNV dbSNP153 33..33 33 - - - 11257 RMVar_ID_11257 Human_SNP_ID_228196029 A-to-I Human chr5 - 37289045 37289045 37289045 TTTTATGAGACTGAGTTTTGCTCTTGTTGCCCAGGCTGGAGTGCAATGGCACGATCTTGGCTCAC TTTTATGAGACTGAGTTTTGCTCTTGTTGCCCGGGCTGGAGTGCAATGGCACGATCTTGGCTCAC T C NUP155 Ensembl:ENSG00000113569 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1276559485 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7436085,Human_RBP_ID_15441492,Human_RBP_ID_23193565,Human_RBP_ID_24506571 Human_miRNA_ID_1076844,Human_miRNA_ID_1159234 11258 RMVar_ID_11258 Human_SNP_ID_228196295 A-to-I Human chr5 - 37290219 37290219 37290219 CCCGCCTCCACCTCCCAAAGTGTTGAGATTACAGACGTGAGCCAATGTGCCTGGCCTATTCCCTT CCCGCCTCCACCTCCCAAAGTGTTGAGATTACGGACGTGAGCCAATGTGCCTGGCCTATTCCCTT T C NUP155 Ensembl:ENSG00000113569 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs993945419 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_641999,Human_RBP_ID_3769751,Human_RBP_ID_7436126,Human_RBP_ID_8213428,Human_RBP_ID_15441555,Human_RBP_ID_24105426 11259 RMVar_ID_11259 Human_SNP_ID_228196296 A-to-I Human chr5 - 37290221 37290221 37290221 TGCCCGCCTCCACCTCCCAAAGTGTTGAGATTACAGACGTGAGCCAATGTGCCTGGCCTATTCCC TGCCCGCCTCCACCTCCCAAAGTGTTGAGATTTCAGACGTGAGCCAATGTGCCTGGCCTATTCCC T A NUP155 Ensembl:ENSG00000113569 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1244392768 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_641999,Human_RBP_ID_3769751,Human_RBP_ID_4830767,Human_RBP_ID_7436126,Human_RBP_ID_8213428,Human_RBP_ID_15441555,Human_RBP_ID_21167135,Human_RBP_ID_23193579,Human_RBP_ID_24105426 11260 RMVar_ID_11260 Human_SNP_ID_228196300 A-to-I Human chr5 - 37290233 37290232 37290234 CCTCAAGTGATCTGCCCGCCTCCACCTCCCAAAGTGTTGAGATTACAGACGTGAGCCAATGTGCC CCTCAAGTGATCTGCCCGCCTCCACCTCCCA__GTGTTGAGATTACAGACGTGAGCCAATGTGCC CTT C NUP155 Ensembl:ENSG00000113569 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1394859871 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_641999,Human_RBP_ID_3769751,Human_RBP_ID_15441555 Human_miRNA_ID_1529928,Human_miRNA_ID_1537559 11261 RMVar_ID_11261 Human_SNP_ID_228196300 A-to-I Human chr5 - 37290234 37290232 37290234 ACCTCAAGTGATCTGCCCGCCTCCACCTCCCAAAGTGTTGAGATTACAGACGTGAGCCAATGTGC ACCTCAAGTGATCTGCCCGCCTCCACCTCCCA__GTGTTGAGATTACAGACGTGAGCCAATGTGC CTT C NUP155 Ensembl:ENSG00000113569 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1394859871 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_641999,Human_RBP_ID_3769751,Human_RBP_ID_15441555 Human_miRNA_ID_1529928,Human_miRNA_ID_1537559 11262 RMVar_ID_11262 Human_SNP_ID_228196312 A-to-I Human chr5 - 37290298 37290298 37290298 TAATTTTTGTATTTTTAGTAGAGATGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGA TAATTTTTGTATTTTTAGTAGAGATGGGTTTCGCCATGTTGGCCAGGCTGGTCTTGAACTCCTGA T C NUP155 Ensembl:ENSG00000113569 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1483532774 Functional Loss SNV dbSNP153 33..33 33 - - - 11263 RMVar_ID_11263 Human_SNP_ID_228196314 A-to-I Human chr5 - 37290311 37290311 37290311 CACCATACCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGTTTCACCATGTTGGCCAGGCTGGT CACCATACCCAGCTAATTTTTGTATTTTTAGTGGAGATGGGTTTCACCATGTTGGCCAGGCTGGT T C NUP155 Ensembl:ENSG00000113569 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs540082910 Functional Loss SNV dbSNP153 33..33 33 - - - 11264 RMVar_ID_11264 Human_SNP_ID_228196325 A-to-I Human chr5 - 37290365 37290365 37290365 TGAAGCAATTTGCCTGCCTCAGCCTCTCGAGTAGCTGGGATTGCAGGTGTGCGCCACCATACCCA TGAAGCAATTTGCCTGCCTCAGCCTCTCGAGTGGCTGGGATTGCAGGTGTGCGCCACCATACCCA T C NUP155 Ensembl:ENSG00000113569 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229,31158229 RNA-Seq:(High) rs903155180 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26531053 11265 RMVar_ID_11265 Human_SNP_ID_228196333 A-to-I Human chr5 - 37290390 37290390 37290390 CACTGCAACCTCTGCCTCACAGGTTTGAAGCAATTTGCCTGCCTCAGCCTCTCGAGTAGCTGGGA CACTGCAACCTCTGCCTCACAGGTTTGAAGCAGTTTGCCTGCCTCAGCCTCTCGAGTAGCTGGGA T C NUP155 Ensembl:ENSG00000113569 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1206924333 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18358339 11266 RMVar_ID_11266 Human_SNP_ID_228196346 A-to-I Human chr5 - 37290464 37290464 37290464 TCTCTTTTTTTTTTTTTTGGAGACAGAATCTCACCCTGTAGCCCAGCCTGGAGTGCAGTGGTGCG TCTCTTTTTTTTTTTTTTGGAGACAGAATCTCGCCCTGTAGCCCAGCCTGGAGTGCAGTGGTGCG T C NUP155 Ensembl:ENSG00000113569 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1344415733 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7436136,Human_RBP_ID_8213429,Human_RBP_ID_22372106,Human_RBP_ID_26529688 11267 RMVar_ID_11267 Human_SNP_ID_228196349 A-to-I Human chr5 - 37290469 37290469 37290469 CTTTCTCTCTTTTTTTTTTTTTTGGAGACAGAATCTCACCCTGTAGCCCAGCCTGGAGTGCAGTG CTTTCTCTCTTTTTTTTTTTTTTGGAGACAGAGTCTCACCCTGTAGCCCAGCCTGGAGTGCAGTG T C NUP155 Ensembl:ENSG00000113569 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1363095202 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7436136,Human_RBP_ID_8213429,Human_RBP_ID_15441563,Human_RBP_ID_22372106,Human_RBP_ID_26529688 11268 RMVar_ID_11268 Human_SNP_ID_228196351 A-to-I Human chr5 - 37290476 37290476 37290476 TCTATTCCTTTCTCTCTTTTTTTTTTTTTTGGAGACAGAATCTCACCCTGTAGCCCAGCCTGGAG TCTATTCCTTTCTCTCTTTTTTTTTTTTTTGGTGACAGAATCTCACCCTGTAGCCCAGCCTGGAG T A NUP155 Ensembl:ENSG00000113569 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1023110638 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7436136,Human_RBP_ID_8213429,Human_RBP_ID_15441563,Human_RBP_ID_22372106,Human_RBP_ID_24506586,Human_RBP_ID_26529688 11269 RMVar_ID_11269 Human_SNP_ID_228196352 A-to-I Human chr5 - 37290476 37290476 37290476 TCTATTCCTTTCTCTCTTTTTTTTTTTTTTGGAGACAGAATCTCACCCTGTAGCCCAGCCTGGAG TCTATTCCTTTCTCTCTTTTTTTTTTTTTTGGCGACAGAATCTCACCCTGTAGCCCAGCCTGGAG T G NUP155 Ensembl:ENSG00000113569 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1023110638 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7436136,Human_RBP_ID_8213429,Human_RBP_ID_15441563,Human_RBP_ID_22372106,Human_RBP_ID_24506586,Human_RBP_ID_26529688 11270 RMVar_ID_11270 Human_SNP_ID_228196565 A-to-I Human chr5 - 37291271 37291267 37291272 CACCATTGCACTCCAGCCCAGGCAACAGGGCGAGACTCTGTCTCAAAAAACAAAAAAACCTCAAA CACCATTGCACTCCAGCCCAGGCAACAGGGC_____TCTGTCTCAAAAAACAAAAAAACCTCAAA AGTCTC A NUP155 Ensembl:ENSG00000113569 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1394161472 Functional Loss DEL dbSNP153 32..36 33 - - - Human_RBP_ID_26526540 11271 RMVar_ID_11271 Human_SNP_ID_228196567 A-to-I Human chr5 - 37291280 37291274 37291281 TCAAAATCGCACCATTGCACTCCAGCCCAGGCAACAGGGCGAGACTCTGTCTCAAAAAACAAAAA TCAAAATCGCACCATTGCACTCCAGCCCAGG_______GCGAGACTCTGTCTCAAAAAACAAAAA CCCTGTTG C NUP155 Ensembl:ENSG00000113569 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886573201 Functional Loss DEL dbSNP153 32..38 33 - - - Human_RBP_ID_23314312 11272 RMVar_ID_11272 Human_SNP_ID_228196572 A-to-I Human chr5 - 37291284 37291284 37291284 TGAGTCAAAATCGCACCATTGCACTCCAGCCCAGGCAACAGGGCGAGACTCTGTCTCAAAAAACA TGAGTCAAAATCGCACCATTGCACTCCAGCCCGGGCAACAGGGCGAGACTCTGTCTCAAAAAACA T C NUP155 Ensembl:ENSG00000113569 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs1429813393 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15441607,Human_RBP_ID_23314312,Human_RBP_ID_25894113 11273 RMVar_ID_11273 Human_SNP_ID_228196583 A-to-I Human chr5 - 37291318 37291318 37291318 CGAATCACTTGAACCCGGGAGGCAGAGGTTTCAGTGAGTCAAAATCGCACCATTGCACTCCAGCC CGAATCACTTGAACCCGGGAGGCAGAGGTTTCGGTGAGTCAAAATCGCACCATTGCACTCCAGCC T C NUP155 Ensembl:ENSG00000113569 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs774274124 Functional Loss SNV dbSNP153 33..33 33 - - - 11274 RMVar_ID_11274 Human_SNP_ID_228196585 A-to-I Human chr5 - 37291327 37291327 37291327 TGAGGGAGGCGAATCACTTGAACCCGGGAGGCAGAGGTTTCAGTGAGTCAAAATCGCACCATTGC TGAGGGAGGCGAATCACTTGAACCCGGGAGGCGGAGGTTTCAGTGAGTCAAAATCGCACCATTGC T C NUP155 Ensembl:ENSG00000113569 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs759408925 Functional Loss SNV dbSNP153 33..33 33 - - - 11275 RMVar_ID_11275 Human_SNP_ID_228196597 A-to-I Human chr5 - 37291353 37291353 37291353 CCTGTAATCCCAGCTACTCGGGAGGCTGAGGGAGGCGAATCACTTGAACCCGGGAGGCAGAGGTT CCTGTAATCCCAGCTACTCGGGAGGCTGAGGGGGGCGAATCACTTGAACCCGGGAGGCAGAGGTT T C NUP155 Ensembl:ENSG00000113569 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1391364720 Functional Loss SNV dbSNP153 33..33 33 - - - 11276 RMVar_ID_11276 Human_SNP_ID_228196603 A-to-I Human chr5 - 37291379 37291379 37291379 AAAATAGCCAGGCGTGGTGGCGGGCGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGGAGGCGAA AAAATAGCCAGGCGTGGTGGCGGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGGAGGCGAA T C NUP155 Ensembl:ENSG00000113569 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs993068349 Functional Loss SNV dbSNP153 33..33 33 - - - 11277 RMVar_ID_11277 Human_SNP_ID_228196616 A-to-I Human chr5 - 37291402 37291402 37291402 CATCTCTACTAAAAATACAAAAAAAAATAGCCAGGCGTGGTGGCGGGCGCCTGTAATCCCAGCTA CATCTCTACTAAAAATACAAAAAAAAATAGCCGGGCGTGGTGGCGGGCGCCTGTAATCCCAGCTA T C NUP155 Ensembl:ENSG00000113569 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs930719689 Functional Loss SNV dbSNP153 33..33 33 - - - 11278 RMVar_ID_11278 Human_SNP_ID_228196630 A-to-I Human chr5 - 37291446 37291443 37291446 GAGGCCAAGAGTTTGAGACCAACCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAA GAGGCCAAGAGTTTGAGACCAACCTGGCCAAC___GTGAAACCCCATCTCTACTAAAAATACAAA CCAT C NUP155 Ensembl:ENSG00000113569 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs775315369 Functional Loss DEL dbSNP153 33..35 33 - - - 11279 RMVar_ID_11279 Human_SNP_ID_228196638 A-to-I Human chr5 - 37291457 37291457 37291457 GGGCGAATCACGAGGCCAAGAGTTTGAGACCAACCTGGCCAACATGGTGAAACCCCATCTCTACT GGGCGAATCACGAGGCCAAGAGTTTGAGACCATCCTGGCCAACATGGTGAAACCCCATCTCTACT T A NUP155 Ensembl:ENSG00000113569 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1209750429 Functional Loss SNV dbSNP153 33..33 33 - - - 11280 RMVar_ID_11280 Human_SNP_ID_228196650 A-to-I Human chr5 - 37291515 37291515 37291515 TAGGCGGCCAGGCACAGTGACTTACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGCGAA TAGGCGGCCAGGCACAGTGACTTACACCTGTATTCCCAGCACTTTGGGAGGCCAAGGTGGGCGAA T A NUP155 Ensembl:ENSG00000113569 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs780502022 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8213432 Human_miRNA_ID_58410,Human_miRNA_ID_1359962 11281 RMVar_ID_11281 Human_SNP_ID_228196654 A-to-I Human chr5 - 37291528 37291528 37291528 ATTAAAACTCCACTAGGCGGCCAGGCACAGTGACTTACACCTGTAATCCCAGCACTTTGGGAGGC ATTAAAACTCCACTAGGCGGCCAGGCACAGTGCCTTACACCTGTAATCCCAGCACTTTGGGAGGC T G NUP155 Ensembl:ENSG00000113569 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs999810622 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7436169,Human_RBP_ID_8213432 Human_miRNA_ID_58410,Human_miRNA_ID_651160,Human_miRNA_ID_1359962 11282 RMVar_ID_11282 Human_SNP_ID_228196657 A-to-I Human chr5 - 37291538 37291538 37291538 GGATATTGGCATTAAAACTCCACTAGGCGGCCAGGCACAGTGACTTACACCTGTAATCCCAGCAC GGATATTGGCATTAAAACTCCACTAGGCGGCCTGGCACAGTGACTTACACCTGTAATCCCAGCAC T A NUP155 Ensembl:ENSG00000113569 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs370795771 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7436169,Human_RBP_ID_8213432,Human_RBP_ID_15441608,Human_RBP_ID_23193602,Human_RBP_ID_24506589 Human_miRNA_ID_651160 11283 RMVar_ID_11283 Human_SNP_ID_228200769 A-to-I Human chr5 - 37305674 37305674 37305674 GTTTTGTTTTTTGTTCGTTTGTTTTTTGAGACAGGGTCTTGCTGTCACCCAGGATGGAGTGCAGT GTTTTGTTTTTTGTTCGTTTGTTTTTTGAGACGGGGTCTTGCTGTCACCCAGGATGGAGTGCAGT T C NUP155 Ensembl:ENSG00000113569 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1229704064 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15441801,Human_RBP_ID_25894255 RMVar_hsa_circ_231012,RMVar_hsa_circ_2246,RMVar_hsa_circ_101911,RMVar_hsa_circ_126099,RMVar_hsa_circ_111251,RMVar_hsa_circ_123265,RMVar_hsa_circ_109573,RMVar_hsa_circ_230993,RMVar_hsa_circ_230997,RMVar_hsa_circ_81202,RMVar_hsa_circ_230995,RMVar_hsa_circ_230996,RMVar_hsa_circ_230994,RMVar_hsa_circ_350599,RMVar_hsa_circ_230992,RMVar_hsa_circ_360032,RMVar_hsa_circ_326231,RMVar_hsa_circ_54035,RMVar_hsa_circ_121461,RMVar_hsa_circ_346415,RMVar_hsa_circ_231005,RMVar_hsa_circ_375908,RMVar_hsa_circ_269398,RMVar_hsa_circ_21906,RMVar_hsa_circ_70004,RMVar_hsa_circ_9035,RMVar_hsa_circ_231006,RMVar_hsa_circ_231007,RMVar_hsa_circ_105548,RMVar_hsa_circ_87874,RMVar_hsa_circ_345113,RMVar_hsa_circ_372459,RMVar_hsa_circ_231010,RMVar_hsa_circ_368408,RMVar_hsa_circ_358525,RMVar_hsa_circ_304685,RMVar_hsa_circ_327563,RMVar_hsa_circ_108271,RMVar_hsa_circ_123506,RMVar_hsa_circ_106354,RMVar_hsa_circ_231016,RMVar_hsa_circ_43625,RMVar_hsa_circ_231017,RMVar_hsa_circ_231014,RMVar_hsa_circ_231015,RMVar_hsa_circ_231013,RMVar_hsa_circ_231021,RMVar_hsa_circ_6328,RMVar_hsa_circ_322783,RMVar_hsa_circ_367314,RMVar_hsa_circ_231011,RMVar_hsa_circ_369285,RMVar_hsa_circ_355207,RMVar_hsa_circ_322456,RMVar_hsa_circ_109758,RMVar_hsa_circ_80530,RMVar_hsa_circ_231023,RMVar_hsa_circ_231025,RMVar_hsa_circ_231026,RMVar_hsa_circ_231024,RMVar_hsa_circ_231022,RMVar_hsa_circ_63591,RMVar_hsa_circ_108398,RMVar_hsa_circ_125515,RMVar_hsa_circ_231029,RMVar_hsa_circ_231030,RMVar_hsa_circ_293849,RMVar_hsa_circ_364765,RMVar_hsa_circ_66252,RMVar_hsa_circ_17471,RMVar_hsa_circ_51062,RMVar_hsa_circ_23925,RMVar_hsa_circ_231032 11284 RMVar_ID_11284 Human_SNP_ID_228201085 A-to-I Human chr5 - 37307050 37307050 37307050 GGGATTACAGGTGCACACCACCACGCCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCA GGGATTACAGGTGCACACCACCACGCCTGGCTGATTTTTGTATTTTTAGTAGAGACAGGGTTTCA T C NUP155 Ensembl:ENSG00000113569 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1469374572 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_231012,RMVar_hsa_circ_2246,RMVar_hsa_circ_101911,RMVar_hsa_circ_126099,RMVar_hsa_circ_111251,RMVar_hsa_circ_123265,RMVar_hsa_circ_109573,RMVar_hsa_circ_230993,RMVar_hsa_circ_230997,RMVar_hsa_circ_81202,RMVar_hsa_circ_230995,RMVar_hsa_circ_230996,RMVar_hsa_circ_230994,RMVar_hsa_circ_350599,RMVar_hsa_circ_230992,RMVar_hsa_circ_360032,RMVar_hsa_circ_326231,RMVar_hsa_circ_54035,RMVar_hsa_circ_121461,RMVar_hsa_circ_346415,RMVar_hsa_circ_231005,RMVar_hsa_circ_375908,RMVar_hsa_circ_269398,RMVar_hsa_circ_21906,RMVar_hsa_circ_70004,RMVar_hsa_circ_9035,RMVar_hsa_circ_231006,RMVar_hsa_circ_231007,RMVar_hsa_circ_105548,RMVar_hsa_circ_87874,RMVar_hsa_circ_345113,RMVar_hsa_circ_372459,RMVar_hsa_circ_231010,RMVar_hsa_circ_368408,RMVar_hsa_circ_358525,RMVar_hsa_circ_304685,RMVar_hsa_circ_327563,RMVar_hsa_circ_108271,RMVar_hsa_circ_123506,RMVar_hsa_circ_106354,RMVar_hsa_circ_231016,RMVar_hsa_circ_43625,RMVar_hsa_circ_231017,RMVar_hsa_circ_231014,RMVar_hsa_circ_231015,RMVar_hsa_circ_231013,RMVar_hsa_circ_231021,RMVar_hsa_circ_6328,RMVar_hsa_circ_322783,RMVar_hsa_circ_367314,RMVar_hsa_circ_231011,RMVar_hsa_circ_369285,RMVar_hsa_circ_355207,RMVar_hsa_circ_322456,RMVar_hsa_circ_109758,RMVar_hsa_circ_80530,RMVar_hsa_circ_231023,RMVar_hsa_circ_231025,RMVar_hsa_circ_231026,RMVar_hsa_circ_231024,RMVar_hsa_circ_231022,RMVar_hsa_circ_63591,RMVar_hsa_circ_108398,RMVar_hsa_circ_125515,RMVar_hsa_circ_231029,RMVar_hsa_circ_231030,RMVar_hsa_circ_293849,RMVar_hsa_circ_364765,RMVar_hsa_circ_66252,RMVar_hsa_circ_17471,RMVar_hsa_circ_51062,RMVar_hsa_circ_23925,RMVar_hsa_circ_231032 11285 RMVar_ID_11285 Human_SNP_ID_228201106 A-to-I Human chr5 - 37307111 37307111 37307111 TCACTGCAATCTCTGCCTCCCAGGTTCAAGCTATTCTCGTGCCTCAGCCTCCCATGTAGCTGGGA TCACTGCAATCTCTGCCTCCCAGGTTCAAGCTGTTCTCGTGCCTCAGCCTCCCATGTAGCTGGGA T C NUP155 Ensembl:ENSG00000113569 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1166891117 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_231012,RMVar_hsa_circ_2246,RMVar_hsa_circ_101911,RMVar_hsa_circ_126099,RMVar_hsa_circ_111251,RMVar_hsa_circ_123265,RMVar_hsa_circ_109573,RMVar_hsa_circ_230993,RMVar_hsa_circ_230997,RMVar_hsa_circ_81202,RMVar_hsa_circ_230995,RMVar_hsa_circ_230996,RMVar_hsa_circ_230994,RMVar_hsa_circ_350599,RMVar_hsa_circ_230992,RMVar_hsa_circ_360032,RMVar_hsa_circ_326231,RMVar_hsa_circ_54035,RMVar_hsa_circ_121461,RMVar_hsa_circ_346415,RMVar_hsa_circ_231005,RMVar_hsa_circ_375908,RMVar_hsa_circ_269398,RMVar_hsa_circ_21906,RMVar_hsa_circ_70004,RMVar_hsa_circ_9035,RMVar_hsa_circ_231006,RMVar_hsa_circ_231007,RMVar_hsa_circ_105548,RMVar_hsa_circ_87874,RMVar_hsa_circ_345113,RMVar_hsa_circ_372459,RMVar_hsa_circ_231010,RMVar_hsa_circ_368408,RMVar_hsa_circ_358525,RMVar_hsa_circ_304685,RMVar_hsa_circ_327563,RMVar_hsa_circ_108271,RMVar_hsa_circ_123506,RMVar_hsa_circ_106354,RMVar_hsa_circ_231016,RMVar_hsa_circ_43625,RMVar_hsa_circ_231017,RMVar_hsa_circ_231014,RMVar_hsa_circ_231015,RMVar_hsa_circ_231013,RMVar_hsa_circ_231021,RMVar_hsa_circ_6328,RMVar_hsa_circ_322783,RMVar_hsa_circ_367314,RMVar_hsa_circ_231011,RMVar_hsa_circ_369285,RMVar_hsa_circ_355207,RMVar_hsa_circ_322456,RMVar_hsa_circ_109758,RMVar_hsa_circ_80530,RMVar_hsa_circ_231023,RMVar_hsa_circ_231025,RMVar_hsa_circ_231026,RMVar_hsa_circ_231024,RMVar_hsa_circ_231022,RMVar_hsa_circ_63591,RMVar_hsa_circ_108398,RMVar_hsa_circ_125515,RMVar_hsa_circ_231029,RMVar_hsa_circ_231030,RMVar_hsa_circ_293849,RMVar_hsa_circ_364765,RMVar_hsa_circ_66252,RMVar_hsa_circ_17471,RMVar_hsa_circ_51062,RMVar_hsa_circ_23925,RMVar_hsa_circ_231032 11286 RMVar_ID_11286 Human_SNP_ID_228201109 A-to-I Human chr5 - 37307122 37307122 37307122 GTGATCTTGGCTCACTGCAATCTCTGCCTCCCAGGTTCAAGCTATTCTCGTGCCTCAGCCTCCCA GTGATCTTGGCTCACTGCAATCTCTGCCTCCCTGGTTCAAGCTATTCTCGTGCCTCAGCCTCCCA T A NUP155 Ensembl:ENSG00000113569 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1399855240 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_231012,RMVar_hsa_circ_2246,RMVar_hsa_circ_101911,RMVar_hsa_circ_126099,RMVar_hsa_circ_111251,RMVar_hsa_circ_123265,RMVar_hsa_circ_109573,RMVar_hsa_circ_230993,RMVar_hsa_circ_230997,RMVar_hsa_circ_81202,RMVar_hsa_circ_230995,RMVar_hsa_circ_230996,RMVar_hsa_circ_230994,RMVar_hsa_circ_350599,RMVar_hsa_circ_230992,RMVar_hsa_circ_360032,RMVar_hsa_circ_326231,RMVar_hsa_circ_54035,RMVar_hsa_circ_121461,RMVar_hsa_circ_346415,RMVar_hsa_circ_231005,RMVar_hsa_circ_375908,RMVar_hsa_circ_269398,RMVar_hsa_circ_21906,RMVar_hsa_circ_70004,RMVar_hsa_circ_9035,RMVar_hsa_circ_231006,RMVar_hsa_circ_231007,RMVar_hsa_circ_105548,RMVar_hsa_circ_87874,RMVar_hsa_circ_345113,RMVar_hsa_circ_372459,RMVar_hsa_circ_231010,RMVar_hsa_circ_368408,RMVar_hsa_circ_358525,RMVar_hsa_circ_304685,RMVar_hsa_circ_327563,RMVar_hsa_circ_108271,RMVar_hsa_circ_123506,RMVar_hsa_circ_106354,RMVar_hsa_circ_231016,RMVar_hsa_circ_43625,RMVar_hsa_circ_231017,RMVar_hsa_circ_231014,RMVar_hsa_circ_231015,RMVar_hsa_circ_231013,RMVar_hsa_circ_231021,RMVar_hsa_circ_6328,RMVar_hsa_circ_322783,RMVar_hsa_circ_367314,RMVar_hsa_circ_231011,RMVar_hsa_circ_369285,RMVar_hsa_circ_355207,RMVar_hsa_circ_322456,RMVar_hsa_circ_109758,RMVar_hsa_circ_80530,RMVar_hsa_circ_231023,RMVar_hsa_circ_231025,RMVar_hsa_circ_231026,RMVar_hsa_circ_231024,RMVar_hsa_circ_231022,RMVar_hsa_circ_63591,RMVar_hsa_circ_108398,RMVar_hsa_circ_125515,RMVar_hsa_circ_231029,RMVar_hsa_circ_231030,RMVar_hsa_circ_293849,RMVar_hsa_circ_364765,RMVar_hsa_circ_66252,RMVar_hsa_circ_17471,RMVar_hsa_circ_51062,RMVar_hsa_circ_23925,RMVar_hsa_circ_231032 11287 RMVar_ID_11287 Human_SNP_ID_228202920 A-to-I Human chr5 - 37313769 37313769 37313769 ACTGGGCACCATGCCTCACGCCTGTGATCCCAACACTTTGGTAGGCTGAGGCAGGAGGATCACTT ACTGGGCACCATGCCTCACGCCTGTGATCCCAGCACTTTGGTAGGCTGAGGCAGGAGGATCACTT T C NUP155 Ensembl:ENSG00000113569 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1036617177 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_231012,RMVar_hsa_circ_101911,RMVar_hsa_circ_126099,RMVar_hsa_circ_111251,RMVar_hsa_circ_123265,RMVar_hsa_circ_109573,RMVar_hsa_circ_230993,RMVar_hsa_circ_230997,RMVar_hsa_circ_81202,RMVar_hsa_circ_230995,RMVar_hsa_circ_230996,RMVar_hsa_circ_230994,RMVar_hsa_circ_230992,RMVar_hsa_circ_360032,RMVar_hsa_circ_54035,RMVar_hsa_circ_121461,RMVar_hsa_circ_375908,RMVar_hsa_circ_269398,RMVar_hsa_circ_21906,RMVar_hsa_circ_70004,RMVar_hsa_circ_9035,RMVar_hsa_circ_231006,RMVar_hsa_circ_231007,RMVar_hsa_circ_105548,RMVar_hsa_circ_87874,RMVar_hsa_circ_231010,RMVar_hsa_circ_368408,RMVar_hsa_circ_358525,RMVar_hsa_circ_327563,RMVar_hsa_circ_108271,RMVar_hsa_circ_123506,RMVar_hsa_circ_106354,RMVar_hsa_circ_231014,RMVar_hsa_circ_231015,RMVar_hsa_circ_231013,RMVar_hsa_circ_231021,RMVar_hsa_circ_6328,RMVar_hsa_circ_231011,RMVar_hsa_circ_369285,RMVar_hsa_circ_355207,RMVar_hsa_circ_109758,RMVar_hsa_circ_80530,RMVar_hsa_circ_231023,RMVar_hsa_circ_231024,RMVar_hsa_circ_231022,RMVar_hsa_circ_108398,RMVar_hsa_circ_125515,RMVar_hsa_circ_231029,RMVar_hsa_circ_231030,RMVar_hsa_circ_293849,RMVar_hsa_circ_66252,RMVar_hsa_circ_17471,RMVar_hsa_circ_51062,RMVar_hsa_circ_231032,RMVar_hsa_circ_68748,RMVar_hsa_circ_21795,RMVar_hsa_circ_54734,RMVar_hsa_circ_71074,RMVar_hsa_circ_75480,RMVar_hsa_circ_25049,RMVar_hsa_circ_231034,RMVar_hsa_circ_3168,RMVar_hsa_circ_376236 11288 RMVar_ID_11288 Human_SNP_ID_228208420 A-to-I Human chr5 - 37334199 37334199 37334199 ACTTGGGAGGTTGAGGTGGGAGAATCAACTGAACCCAGGGAGGTCGAGGTTGCAGTGAGTTGTGA ACTTGGGAGGTTGAGGTGGGAGAATCAACTGACCCCAGGGAGGTCGAGGTTGCAGTGAGTTGTGA T G NUP155 Ensembl:ENSG00000113569 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs369972262 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15442492 RMVar_hsa_circ_231012,RMVar_hsa_circ_54035,RMVar_hsa_circ_375908,RMVar_hsa_circ_269398,RMVar_hsa_circ_70004,RMVar_hsa_circ_9035,RMVar_hsa_circ_231006,RMVar_hsa_circ_105548,RMVar_hsa_circ_87874,RMVar_hsa_circ_231010,RMVar_hsa_circ_368408,RMVar_hsa_circ_106354,RMVar_hsa_circ_4941,RMVar_hsa_circ_231021,RMVar_hsa_circ_231011,RMVar_hsa_circ_369285,RMVar_hsa_circ_80530,RMVar_hsa_circ_231022,RMVar_hsa_circ_108398,RMVar_hsa_circ_125515,RMVar_hsa_circ_231029,RMVar_hsa_circ_231030,RMVar_hsa_circ_17471,RMVar_hsa_circ_231032,RMVar_hsa_circ_68748,RMVar_hsa_circ_75480,RMVar_hsa_circ_25049,RMVar_hsa_circ_347950,RMVar_hsa_circ_370301,RMVar_hsa_circ_231037,RMVar_hsa_circ_328141,RMVar_hsa_circ_364515,RMVar_hsa_circ_71622,RMVar_hsa_circ_378297,RMVar_hsa_circ_79052,RMVar_hsa_circ_31341,RMVar_hsa_circ_231042,RMVar_hsa_circ_302170,RMVar_hsa_circ_310220,RMVar_hsa_circ_100330,RMVar_hsa_circ_231046,RMVar_hsa_circ_231048,RMVar_hsa_circ_90056,RMVar_hsa_circ_231047,RMVar_hsa_circ_231045,RMVar_hsa_circ_364708,RMVar_hsa_circ_38422,RMVar_hsa_circ_14120,RMVar_hsa_circ_27365,RMVar_hsa_circ_47382,RMVar_hsa_circ_354702,RMVar_hsa_circ_276394,RMVar_hsa_circ_362601,RMVar_hsa_circ_231052,RMVar_hsa_circ_325935,RMVar_hsa_circ_272044,RMVar_hsa_circ_231055 11289 RMVar_ID_11289 Human_SNP_ID_228208524 A-to-I Human chr5 - 37334537 37334537 37334537 GTCTCTAATAACAATACAAAAATTAGCCGGGTATGGTGGTGTGCGTCTCTAATCCCAGATACTCG GTCTCTAATAACAATACAAAAATTAGCCGGGTGTGGTGGTGTGCGTCTCTAATCCCAGATACTCG T C NUP155 Ensembl:ENSG00000113569 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1057070968 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_231012,RMVar_hsa_circ_54035,RMVar_hsa_circ_375908,RMVar_hsa_circ_269398,RMVar_hsa_circ_70004,RMVar_hsa_circ_9035,RMVar_hsa_circ_231006,RMVar_hsa_circ_105548,RMVar_hsa_circ_87874,RMVar_hsa_circ_231010,RMVar_hsa_circ_368408,RMVar_hsa_circ_106354,RMVar_hsa_circ_4941,RMVar_hsa_circ_231021,RMVar_hsa_circ_231011,RMVar_hsa_circ_369285,RMVar_hsa_circ_80530,RMVar_hsa_circ_231022,RMVar_hsa_circ_108398,RMVar_hsa_circ_125515,RMVar_hsa_circ_231029,RMVar_hsa_circ_231030,RMVar_hsa_circ_17471,RMVar_hsa_circ_231032,RMVar_hsa_circ_68748,RMVar_hsa_circ_75480,RMVar_hsa_circ_25049,RMVar_hsa_circ_347950,RMVar_hsa_circ_370301,RMVar_hsa_circ_231037,RMVar_hsa_circ_328141,RMVar_hsa_circ_364515,RMVar_hsa_circ_71622,RMVar_hsa_circ_378297,RMVar_hsa_circ_79052,RMVar_hsa_circ_31341,RMVar_hsa_circ_231042,RMVar_hsa_circ_302170,RMVar_hsa_circ_310220,RMVar_hsa_circ_100330,RMVar_hsa_circ_231046,RMVar_hsa_circ_231048,RMVar_hsa_circ_90056,RMVar_hsa_circ_231047,RMVar_hsa_circ_231045,RMVar_hsa_circ_364708,RMVar_hsa_circ_38422,RMVar_hsa_circ_14120,RMVar_hsa_circ_27365,RMVar_hsa_circ_47382,RMVar_hsa_circ_354702,RMVar_hsa_circ_276394,RMVar_hsa_circ_362601,RMVar_hsa_circ_231052,RMVar_hsa_circ_325935,RMVar_hsa_circ_272044,RMVar_hsa_circ_231055 11290 RMVar_ID_11290 Human_SNP_ID_228208874 A-to-I Human chr5 - 37335739 37335739 37335739 TGCCATGTAGCCCCTGCTGGTCTCGAATTCCTAAGCTTAAGGGATCCACCTGCCTTGGTCTCCCA TGCCATGTAGCCCCTGCTGGTCTCGAATTCCTGAGCTTAAGGGATCCACCTGCCTTGGTCTCCCA T C NUP155 Ensembl:ENSG00000113569 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1191555911 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_231012,RMVar_hsa_circ_54035,RMVar_hsa_circ_375908,RMVar_hsa_circ_269398,RMVar_hsa_circ_70004,RMVar_hsa_circ_9035,RMVar_hsa_circ_231006,RMVar_hsa_circ_105548,RMVar_hsa_circ_87874,RMVar_hsa_circ_231010,RMVar_hsa_circ_368408,RMVar_hsa_circ_106354,RMVar_hsa_circ_4941,RMVar_hsa_circ_231021,RMVar_hsa_circ_231011,RMVar_hsa_circ_369285,RMVar_hsa_circ_80530,RMVar_hsa_circ_231022,RMVar_hsa_circ_108398,RMVar_hsa_circ_125515,RMVar_hsa_circ_231029,RMVar_hsa_circ_231030,RMVar_hsa_circ_17471,RMVar_hsa_circ_231032,RMVar_hsa_circ_68748,RMVar_hsa_circ_75480,RMVar_hsa_circ_25049,RMVar_hsa_circ_347950,RMVar_hsa_circ_370301,RMVar_hsa_circ_231037,RMVar_hsa_circ_328141,RMVar_hsa_circ_364515,RMVar_hsa_circ_71622,RMVar_hsa_circ_378297,RMVar_hsa_circ_79052,RMVar_hsa_circ_31341,RMVar_hsa_circ_231042,RMVar_hsa_circ_302170,RMVar_hsa_circ_310220,RMVar_hsa_circ_100330,RMVar_hsa_circ_231046,RMVar_hsa_circ_231048,RMVar_hsa_circ_90056,RMVar_hsa_circ_231047,RMVar_hsa_circ_231045,RMVar_hsa_circ_364708,RMVar_hsa_circ_38422,RMVar_hsa_circ_14120,RMVar_hsa_circ_27365,RMVar_hsa_circ_47382,RMVar_hsa_circ_354702,RMVar_hsa_circ_276394,RMVar_hsa_circ_362601,RMVar_hsa_circ_231052,RMVar_hsa_circ_325935,RMVar_hsa_circ_272044,RMVar_hsa_circ_231055 11291 RMVar_ID_11291 Human_SNP_ID_228209020 A-to-I Human chr5 - 37336296 37336296 37336296 TTAAATTTTTTGTAGCGACAGGGTCTGACTATATTGCCCAGACTAGTCTTGAACTCCTGGGCTCA TTAAATTTTTTGTAGCGACAGGGTCTGACTATGTTGCCCAGACTAGTCTTGAACTCCTGGGCTCA T C NUP155 Ensembl:ENSG00000113569 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1260389581 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15442544 RMVar_hsa_circ_231012,RMVar_hsa_circ_54035,RMVar_hsa_circ_375908,RMVar_hsa_circ_269398,RMVar_hsa_circ_70004,RMVar_hsa_circ_9035,RMVar_hsa_circ_231006,RMVar_hsa_circ_105548,RMVar_hsa_circ_87874,RMVar_hsa_circ_231010,RMVar_hsa_circ_368408,RMVar_hsa_circ_106354,RMVar_hsa_circ_4941,RMVar_hsa_circ_231021,RMVar_hsa_circ_231011,RMVar_hsa_circ_369285,RMVar_hsa_circ_80530,RMVar_hsa_circ_231022,RMVar_hsa_circ_108398,RMVar_hsa_circ_125515,RMVar_hsa_circ_231029,RMVar_hsa_circ_231030,RMVar_hsa_circ_17471,RMVar_hsa_circ_231032,RMVar_hsa_circ_68748,RMVar_hsa_circ_75480,RMVar_hsa_circ_25049,RMVar_hsa_circ_347950,RMVar_hsa_circ_370301,RMVar_hsa_circ_231037,RMVar_hsa_circ_328141,RMVar_hsa_circ_364515,RMVar_hsa_circ_71622,RMVar_hsa_circ_378297,RMVar_hsa_circ_79052,RMVar_hsa_circ_31341,RMVar_hsa_circ_231042,RMVar_hsa_circ_302170,RMVar_hsa_circ_310220,RMVar_hsa_circ_100330,RMVar_hsa_circ_231046,RMVar_hsa_circ_231048,RMVar_hsa_circ_90056,RMVar_hsa_circ_231047,RMVar_hsa_circ_231045,RMVar_hsa_circ_364708,RMVar_hsa_circ_38422,RMVar_hsa_circ_14120,RMVar_hsa_circ_27365,RMVar_hsa_circ_47382,RMVar_hsa_circ_354702,RMVar_hsa_circ_276394,RMVar_hsa_circ_362601,RMVar_hsa_circ_231052,RMVar_hsa_circ_325935,RMVar_hsa_circ_272044,RMVar_hsa_circ_231055 11292 RMVar_ID_11292 Human_SNP_ID_228209531 A-to-I Human chr5 - 37338266 37338266 37338266 GCGCCCAGGCTGGAGTGCAGTGGCACAATCTCAGCTTACTGCAACCTCCACCTCCTGCGTTCACG GCGCCCAGGCTGGAGTGCAGTGGCACAATCTCTGCTTACTGCAACCTCCACCTCCTGCGTTCACG T A NUP155 Ensembl:ENSG00000113569 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs570131840 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54035,RMVar_hsa_circ_375908,RMVar_hsa_circ_269398,RMVar_hsa_circ_70004,RMVar_hsa_circ_9035,RMVar_hsa_circ_231006,RMVar_hsa_circ_368408,RMVar_hsa_circ_106354,RMVar_hsa_circ_4941,RMVar_hsa_circ_231021,RMVar_hsa_circ_231011,RMVar_hsa_circ_369285,RMVar_hsa_circ_80530,RMVar_hsa_circ_231022,RMVar_hsa_circ_108398,RMVar_hsa_circ_125515,RMVar_hsa_circ_231029,RMVar_hsa_circ_231030,RMVar_hsa_circ_17471,RMVar_hsa_circ_231032,RMVar_hsa_circ_68748,RMVar_hsa_circ_75480,RMVar_hsa_circ_25049,RMVar_hsa_circ_347950,RMVar_hsa_circ_370301,RMVar_hsa_circ_231037,RMVar_hsa_circ_328141,RMVar_hsa_circ_364515,RMVar_hsa_circ_71622,RMVar_hsa_circ_378297,RMVar_hsa_circ_79052,RMVar_hsa_circ_31341,RMVar_hsa_circ_231042,RMVar_hsa_circ_302170,RMVar_hsa_circ_310220,RMVar_hsa_circ_100330,RMVar_hsa_circ_231046,RMVar_hsa_circ_231048,RMVar_hsa_circ_90056,RMVar_hsa_circ_231047,RMVar_hsa_circ_231045,RMVar_hsa_circ_364708,RMVar_hsa_circ_38422,RMVar_hsa_circ_14120,RMVar_hsa_circ_27365,RMVar_hsa_circ_47382,RMVar_hsa_circ_354702,RMVar_hsa_circ_276394,RMVar_hsa_circ_362601,RMVar_hsa_circ_231052,RMVar_hsa_circ_325935,RMVar_hsa_circ_272044,RMVar_hsa_circ_26708,RMVar_hsa_circ_231055,RMVar_hsa_circ_361987,RMVar_hsa_circ_375726,RMVar_hsa_circ_120846,RMVar_hsa_circ_64771,RMVar_hsa_circ_231057,RMVar_hsa_circ_231058 11293 RMVar_ID_11293 Human_SNP_ID_228209532 A-to-I Human chr5 - 37338266 37338266 37338266 GCGCCCAGGCTGGAGTGCAGTGGCACAATCTCAGCTTACTGCAACCTCCACCTCCTGCGTTCACG GCGCCCAGGCTGGAGTGCAGTGGCACAATCTCGGCTTACTGCAACCTCCACCTCCTGCGTTCACG T C NUP155 Ensembl:ENSG00000113569 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs570131840 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54035,RMVar_hsa_circ_375908,RMVar_hsa_circ_269398,RMVar_hsa_circ_70004,RMVar_hsa_circ_9035,RMVar_hsa_circ_231006,RMVar_hsa_circ_368408,RMVar_hsa_circ_106354,RMVar_hsa_circ_4941,RMVar_hsa_circ_231021,RMVar_hsa_circ_231011,RMVar_hsa_circ_369285,RMVar_hsa_circ_80530,RMVar_hsa_circ_231022,RMVar_hsa_circ_108398,RMVar_hsa_circ_125515,RMVar_hsa_circ_231029,RMVar_hsa_circ_231030,RMVar_hsa_circ_17471,RMVar_hsa_circ_231032,RMVar_hsa_circ_68748,RMVar_hsa_circ_75480,RMVar_hsa_circ_25049,RMVar_hsa_circ_347950,RMVar_hsa_circ_370301,RMVar_hsa_circ_231037,RMVar_hsa_circ_328141,RMVar_hsa_circ_364515,RMVar_hsa_circ_71622,RMVar_hsa_circ_378297,RMVar_hsa_circ_79052,RMVar_hsa_circ_31341,RMVar_hsa_circ_231042,RMVar_hsa_circ_302170,RMVar_hsa_circ_310220,RMVar_hsa_circ_100330,RMVar_hsa_circ_231046,RMVar_hsa_circ_231048,RMVar_hsa_circ_90056,RMVar_hsa_circ_231047,RMVar_hsa_circ_231045,RMVar_hsa_circ_364708,RMVar_hsa_circ_38422,RMVar_hsa_circ_14120,RMVar_hsa_circ_27365,RMVar_hsa_circ_47382,RMVar_hsa_circ_354702,RMVar_hsa_circ_276394,RMVar_hsa_circ_362601,RMVar_hsa_circ_231052,RMVar_hsa_circ_325935,RMVar_hsa_circ_272044,RMVar_hsa_circ_26708,RMVar_hsa_circ_231055,RMVar_hsa_circ_361987,RMVar_hsa_circ_375726,RMVar_hsa_circ_120846,RMVar_hsa_circ_64771,RMVar_hsa_circ_231057,RMVar_hsa_circ_231058 11294 RMVar_ID_11294 Human_SNP_ID_228210021 A-to-I Human chr5 - 37339935 37339935 37339935 CAACATGGCGAAACCCTGTCTCTACTAAAAATACAAAAATTAGCCGGGTGTAGGGGGCATGTCTG CAACATGGCGAAACCCTGTCTCTACTAAAAATGCAAAAATTAGCCGGGTGTAGGGGGCATGTCTG T C NUP155 Ensembl:ENSG00000113569 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1036237770 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54035,RMVar_hsa_circ_375908,RMVar_hsa_circ_269398,RMVar_hsa_circ_70004,RMVar_hsa_circ_9035,RMVar_hsa_circ_231006,RMVar_hsa_circ_368408,RMVar_hsa_circ_106354,RMVar_hsa_circ_4941,RMVar_hsa_circ_231021,RMVar_hsa_circ_231011,RMVar_hsa_circ_369285,RMVar_hsa_circ_80530,RMVar_hsa_circ_231022,RMVar_hsa_circ_108398,RMVar_hsa_circ_125515,RMVar_hsa_circ_231029,RMVar_hsa_circ_231030,RMVar_hsa_circ_17471,RMVar_hsa_circ_231032,RMVar_hsa_circ_68748,RMVar_hsa_circ_75480,RMVar_hsa_circ_25049,RMVar_hsa_circ_347950,RMVar_hsa_circ_370301,RMVar_hsa_circ_231037,RMVar_hsa_circ_328141,RMVar_hsa_circ_364515,RMVar_hsa_circ_71622,RMVar_hsa_circ_378297,RMVar_hsa_circ_79052,RMVar_hsa_circ_31341,RMVar_hsa_circ_231042,RMVar_hsa_circ_302170,RMVar_hsa_circ_310220,RMVar_hsa_circ_100330,RMVar_hsa_circ_231046,RMVar_hsa_circ_231048,RMVar_hsa_circ_90056,RMVar_hsa_circ_231047,RMVar_hsa_circ_231045,RMVar_hsa_circ_364708,RMVar_hsa_circ_38422,RMVar_hsa_circ_14120,RMVar_hsa_circ_27365,RMVar_hsa_circ_47382,RMVar_hsa_circ_354702,RMVar_hsa_circ_276394,RMVar_hsa_circ_362601,RMVar_hsa_circ_231052,RMVar_hsa_circ_325935,RMVar_hsa_circ_272044,RMVar_hsa_circ_26708,RMVar_hsa_circ_231055,RMVar_hsa_circ_361987,RMVar_hsa_circ_375726,RMVar_hsa_circ_120846,RMVar_hsa_circ_64771,RMVar_hsa_circ_231057,RMVar_hsa_circ_231058 11295 RMVar_ID_11295 Human_SNP_ID_228211137 A-to-I Human chr5 - 37343734 37343734 37343734 CATGCGCTACCACCCCTGGCTAATTTTTTTGTATTTTTAGTAGAGACGGGGGTTCACCATGTTGA CATGCGCTACCACCCCTGGCTAATTTTTTTGTGTTTTTAGTAGAGACGGGGGTTCACCATGTTGA T C NUP155 Ensembl:ENSG00000113569 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs897529285 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15442633 RMVar_hsa_circ_54035,RMVar_hsa_circ_375908,RMVar_hsa_circ_269398,RMVar_hsa_circ_70004,RMVar_hsa_circ_9035,RMVar_hsa_circ_231006,RMVar_hsa_circ_368408,RMVar_hsa_circ_106354,RMVar_hsa_circ_4941,RMVar_hsa_circ_231021,RMVar_hsa_circ_231011,RMVar_hsa_circ_369285,RMVar_hsa_circ_80530,RMVar_hsa_circ_231022,RMVar_hsa_circ_108398,RMVar_hsa_circ_231030,RMVar_hsa_circ_68748,RMVar_hsa_circ_75480,RMVar_hsa_circ_347950,RMVar_hsa_circ_370301,RMVar_hsa_circ_231037,RMVar_hsa_circ_328141,RMVar_hsa_circ_364515,RMVar_hsa_circ_378297,RMVar_hsa_circ_79052,RMVar_hsa_circ_31341,RMVar_hsa_circ_231042,RMVar_hsa_circ_302170,RMVar_hsa_circ_310220,RMVar_hsa_circ_231046,RMVar_hsa_circ_231048,RMVar_hsa_circ_90056,RMVar_hsa_circ_231047,RMVar_hsa_circ_364708,RMVar_hsa_circ_38422,RMVar_hsa_circ_4955,RMVar_hsa_circ_27365,RMVar_hsa_circ_47382,RMVar_hsa_circ_354702,RMVar_hsa_circ_272044,RMVar_hsa_circ_361987,RMVar_hsa_circ_375726,RMVar_hsa_circ_64771,RMVar_hsa_circ_291203,RMVar_hsa_circ_231058,RMVar_hsa_circ_359353,RMVar_hsa_circ_332741,RMVar_hsa_circ_126818,RMVar_hsa_circ_50328,RMVar_hsa_circ_231062,RMVar_hsa_circ_105357,RMVar_hsa_circ_231060,RMVar_hsa_circ_305625,RMVar_hsa_circ_310175,RMVar_hsa_circ_324155,RMVar_hsa_circ_278497,RMVar_hsa_circ_231064,RMVar_hsa_circ_231065,RMVar_hsa_circ_231063,RMVar_hsa_circ_231061 11296 RMVar_ID_11296 Human_SNP_ID_228212094 A-to-I Human chr5 - 37347112 37347112 37347112 GCGATTCTCCCACCTAAGCCTCCCGAGCGGCTAGGACTACAGGCACATGCCACCACACCTGGCGA GCGATTCTCCCACCTAAGCCTCCCGAGCGGCTGGGACTACAGGCACATGCCACCACACCTGGCGA T C NUP155 Ensembl:ENSG00000113569 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053063073 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15442754 RMVar_hsa_circ_54035,RMVar_hsa_circ_375908,RMVar_hsa_circ_269398,RMVar_hsa_circ_70004,RMVar_hsa_circ_9035,RMVar_hsa_circ_231006,RMVar_hsa_circ_368408,RMVar_hsa_circ_106354,RMVar_hsa_circ_4941,RMVar_hsa_circ_231021,RMVar_hsa_circ_231011,RMVar_hsa_circ_369285,RMVar_hsa_circ_80530,RMVar_hsa_circ_231022,RMVar_hsa_circ_108398,RMVar_hsa_circ_231030,RMVar_hsa_circ_68748,RMVar_hsa_circ_75480,RMVar_hsa_circ_347950,RMVar_hsa_circ_370301,RMVar_hsa_circ_231037,RMVar_hsa_circ_328141,RMVar_hsa_circ_364515,RMVar_hsa_circ_378297,RMVar_hsa_circ_79052,RMVar_hsa_circ_31341,RMVar_hsa_circ_231042,RMVar_hsa_circ_302170,RMVar_hsa_circ_310220,RMVar_hsa_circ_231046,RMVar_hsa_circ_231048,RMVar_hsa_circ_90056,RMVar_hsa_circ_231047,RMVar_hsa_circ_364708,RMVar_hsa_circ_38422,RMVar_hsa_circ_4955,RMVar_hsa_circ_27365,RMVar_hsa_circ_47382,RMVar_hsa_circ_354702,RMVar_hsa_circ_272044,RMVar_hsa_circ_361987,RMVar_hsa_circ_375726,RMVar_hsa_circ_64771,RMVar_hsa_circ_291203,RMVar_hsa_circ_231058,RMVar_hsa_circ_359353,RMVar_hsa_circ_332741,RMVar_hsa_circ_126818,RMVar_hsa_circ_50328,RMVar_hsa_circ_231062,RMVar_hsa_circ_105357,RMVar_hsa_circ_231060,RMVar_hsa_circ_305625,RMVar_hsa_circ_310175,RMVar_hsa_circ_324155,RMVar_hsa_circ_278497,RMVar_hsa_circ_231064,RMVar_hsa_circ_231065,RMVar_hsa_circ_231063,RMVar_hsa_circ_231061 11297 RMVar_ID_11297 Human_SNP_ID_228213650 A-to-I Human chr5 - 37352462 37352462 37352462 GTGATCTTGGCTTACCGCATCCTCTGCCTCCCAGGCTCAAGTGATTCTCCTGCTTCAGTCTCTTG GTGATCTTGGCTTACCGCATCCTCTGCCTCCCCGGCTCAAGTGATTCTCCTGCTTCAGTCTCTTG T G NUP155 Ensembl:ENSG00000113569 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1320167453 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54035,RMVar_hsa_circ_375908,RMVar_hsa_circ_70004,RMVar_hsa_circ_9035,RMVar_hsa_circ_231006,RMVar_hsa_circ_368408,RMVar_hsa_circ_106354,RMVar_hsa_circ_231021,RMVar_hsa_circ_231011,RMVar_hsa_circ_369285,RMVar_hsa_circ_80530,RMVar_hsa_circ_231022,RMVar_hsa_circ_108398,RMVar_hsa_circ_231030,RMVar_hsa_circ_68748,RMVar_hsa_circ_75480,RMVar_hsa_circ_347950,RMVar_hsa_circ_370301,RMVar_hsa_circ_231037,RMVar_hsa_circ_364515,RMVar_hsa_circ_378297,RMVar_hsa_circ_31341,RMVar_hsa_circ_302170,RMVar_hsa_circ_310220,RMVar_hsa_circ_231048,RMVar_hsa_circ_231047,RMVar_hsa_circ_364708,RMVar_hsa_circ_38422,RMVar_hsa_circ_47382,RMVar_hsa_circ_354702,RMVar_hsa_circ_272044,RMVar_hsa_circ_361987,RMVar_hsa_circ_375726,RMVar_hsa_circ_64771,RMVar_hsa_circ_291203,RMVar_hsa_circ_231058,RMVar_hsa_circ_332741,RMVar_hsa_circ_126818,RMVar_hsa_circ_50328,RMVar_hsa_circ_231060,RMVar_hsa_circ_310175,RMVar_hsa_circ_278497,RMVar_hsa_circ_231064,RMVar_hsa_circ_231065,RMVar_hsa_circ_231066,RMVar_hsa_circ_311677,RMVar_hsa_circ_289747,RMVar_hsa_circ_231067,RMVar_hsa_circ_231071,RMVar_hsa_circ_304395,RMVar_hsa_circ_296299,RMVar_hsa_circ_231070,RMVar_hsa_circ_231073,RMVar_hsa_circ_280385,RMVar_hsa_circ_291367,RMVar_hsa_circ_344700,RMVar_hsa_circ_231072 11298 RMVar_ID_11298 Human_SNP_ID_228214842 A-to-I Human chr5 - 37356527 37356527 37356527 TCAAGCGATTCTCCTGCCTCAGCCTCTCAAGTAGCTGGGATTATAAACGCATGTCACCACGCCTA TCAAGCGATTCTCCTGCCTCAGCCTCTCAAGTGGCTGGGATTATAAACGCATGTCACCACGCCTA T C NUP155 Ensembl:ENSG00000113569 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1246843314 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54035,RMVar_hsa_circ_375908,RMVar_hsa_circ_70004,RMVar_hsa_circ_231006,RMVar_hsa_circ_368408,RMVar_hsa_circ_106354,RMVar_hsa_circ_231021,RMVar_hsa_circ_231011,RMVar_hsa_circ_369285,RMVar_hsa_circ_108398,RMVar_hsa_circ_231030,RMVar_hsa_circ_68748,RMVar_hsa_circ_75480,RMVar_hsa_circ_347950,RMVar_hsa_circ_364515,RMVar_hsa_circ_31341,RMVar_hsa_circ_310220,RMVar_hsa_circ_231048,RMVar_hsa_circ_364708,RMVar_hsa_circ_38422,RMVar_hsa_circ_47382,RMVar_hsa_circ_354702,RMVar_hsa_circ_272044,RMVar_hsa_circ_361987,RMVar_hsa_circ_64771,RMVar_hsa_circ_291203,RMVar_hsa_circ_126818,RMVar_hsa_circ_50328,RMVar_hsa_circ_231060,RMVar_hsa_circ_278497,RMVar_hsa_circ_231065,RMVar_hsa_circ_231066,RMVar_hsa_circ_289747,RMVar_hsa_circ_231071,RMVar_hsa_circ_304395,RMVar_hsa_circ_231073,RMVar_hsa_circ_291367,RMVar_hsa_circ_371883,RMVar_hsa_circ_289551,RMVar_hsa_circ_231075,RMVar_hsa_circ_231076 11299 RMVar_ID_11299 Human_SNP_ID_228214951 A-to-I Human chr5 - 37356985 37356985 37356985 CTCTTGCCTCAGCCTTCCAAGTAGCTGGGATTACAGGCATGTGCCACCATGCCCAGCTAATTTTT CTCTTGCCTCAGCCTTCCAAGTAGCTGGGATTCCAGGCATGTGCCACCATGCCCAGCTAATTTTT T G NUP155 Ensembl:ENSG00000113569 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs376742702 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54035,RMVar_hsa_circ_375908,RMVar_hsa_circ_70004,RMVar_hsa_circ_231006,RMVar_hsa_circ_368408,RMVar_hsa_circ_106354,RMVar_hsa_circ_231021,RMVar_hsa_circ_231011,RMVar_hsa_circ_369285,RMVar_hsa_circ_108398,RMVar_hsa_circ_231030,RMVar_hsa_circ_68748,RMVar_hsa_circ_75480,RMVar_hsa_circ_347950,RMVar_hsa_circ_364515,RMVar_hsa_circ_31341,RMVar_hsa_circ_310220,RMVar_hsa_circ_231048,RMVar_hsa_circ_364708,RMVar_hsa_circ_38422,RMVar_hsa_circ_47382,RMVar_hsa_circ_354702,RMVar_hsa_circ_272044,RMVar_hsa_circ_361987,RMVar_hsa_circ_64771,RMVar_hsa_circ_291203,RMVar_hsa_circ_126818,RMVar_hsa_circ_50328,RMVar_hsa_circ_231060,RMVar_hsa_circ_278497,RMVar_hsa_circ_231065,RMVar_hsa_circ_231066,RMVar_hsa_circ_289747,RMVar_hsa_circ_231071,RMVar_hsa_circ_304395,RMVar_hsa_circ_231073,RMVar_hsa_circ_291367,RMVar_hsa_circ_371883,RMVar_hsa_circ_289551,RMVar_hsa_circ_231075,RMVar_hsa_circ_231076 11300 RMVar_ID_11300 Human_SNP_ID_228218557 A-to-I Human chr5 - 37368996 37368996 37368996 CTCCTACCTCAGCCTTCCAAAGTGCTGAGATTACAGATGTAAGTCACACTCCTGGCCTGAAGTCT CTCCTACCTCAGCCTTCCAAAGTGCTGAGATTGCAGATGTAAGTCACACTCCTGGCCTGAAGTCT T C NUP155 Ensembl:ENSG00000113569 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1357081325 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97824,RMVar_hsa_circ_231079 11301 RMVar_ID_11301 Human_SNP_ID_228218869 A-to-I Human chr5 - 37370187 37370187 37370187 TTGTGTTTTTTAAGTAGAGACGGGGTTTCACCATATTGGCCTGGCTGGTCACGAACTCTGACCTC TTGTGTTTTTTAAGTAGAGACGGGGTTTCACCTTATTGGCCTGGCTGGTCACGAACTCTGACCTC T A NUP155 Ensembl:ENSG00000113569 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935393405 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15568575 RMVar_hsa_circ_97824,RMVar_hsa_circ_231079 11302 RMVar_ID_11302 Human_SNP_ID_228218870 A-to-I Human chr5 - 37370187 37370187 37370187 TTGTGTTTTTTAAGTAGAGACGGGGTTTCACCATATTGGCCTGGCTGGTCACGAACTCTGACCTC TTGTGTTTTTTAAGTAGAGACGGGGTTTCACCGTATTGGCCTGGCTGGTCACGAACTCTGACCTC T C NUP155 Ensembl:ENSG00000113569 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935393405 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15568575 RMVar_hsa_circ_97824,RMVar_hsa_circ_231079 11303 RMVar_ID_11303 Human_SNP_ID_228218913 A-to-I Human chr5 - 37370333 37370333 37370333 AGCGGTTCCCTCTTCGCCCAGGCTGAAGTGCAATGGCGCGATCTCGGCTCATTGCAACCTCCGCC AGCGGTTCCCTCTTCGCCCAGGCTGAAGTGCAGTGGCGCGATCTCGGCTCATTGCAACCTCCGCC T C NUP155 Ensembl:ENSG00000113569 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934005323 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97824,RMVar_hsa_circ_231079 11304 RMVar_ID_11304 Human_SNP_ID_228226095 A-to-I Human chr5 + 37397953 37397953 37397953 GGGAGACAGAGGTTGCAGTGAGCCGAGATTGCACCACTGCTCTCCAGCCTGGGTGACAGATTCGG GGGAGACAGAGGTTGCAGTGAGCCGAGATTGCGCCACTGCTCTCCAGCCTGGGTGACAGATTCGG A G WDR70 Ensembl:ENSG00000082068 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs897869387 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95615,RMVar_hsa_circ_231080,RMVar_hsa_circ_91922,RMVar_hsa_circ_231081,RMVar_hsa_circ_102618,RMVar_hsa_circ_266250,RMVar_hsa_circ_34780,RMVar_hsa_circ_58155,RMVar_hsa_circ_231082,RMVar_hsa_circ_71178,RMVar_hsa_circ_378206 11305 RMVar_ID_11305 Human_SNP_ID_228265240 A-to-I Human chr5 + 37558600 37558600 37558600 CACCCGCCTCAGCCTCCTAAAGTGCTGAGATTAGAGGCATGAGCCACTGCACCCAGCCCACGTTG CACCCGCCTCAGCCTCCTAAAGTGCTGAGATTGGAGGCATGAGCCACTGCACCCAGCCCACGTTG A G WDR70 Ensembl:ENSG00000082068 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs907405904 Functional Loss SNV 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 11306 RMVar_ID_11306 Human_SNP_ID_228573077 A-to-I Human chr5 - 38823076 38823076 38823076 ACATGTATATGCACATGTGTATACAGGCATGTATATATGTGTGCTTACCTACGAATATACATACA ACATGTATATGCACATGTGTATACAGGCATGTGTATATGTGTGCTTACCTACGAATATACATACA T C OSMR-AS1 Ensembl:ENSG00000249740 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1399968751 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5612151 11307 RMVar_ID_11307 Human_SNP_ID_228576307 A-to-I Human chr5 - 38834332 38834332 38834332 GACTGGGCGTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGTGGATCACC GACTGGGCGTGGTGGCTCACACCTGTAATCCCGGCACTTTGGGAGGCCAAGGTGGGTGGATCACC T C OSMR-AS1 Ensembl:ENSG00000249740 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1234672456 Functional Loss SNV dbSNP153 33..33 33 - - - 11308 RMVar_ID_11308 Human_SNP_ID_228576359 A-to-I Human chr5 - 38834613 38834613 38834613 GCGATCTGGACTCACTGCAACCTTGACCCCCTAGGCCCAAACAATCCCCCCACCTCAGCCCCCAG GCGATCTGGACTCACTGCAACCTTGACCCCCTGGGCCCAAACAATCCCCCCACCTCAGCCCCCAG T C OSMR-AS1 Ensembl:ENSG00000249740 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1339500284 Functional Loss SNV dbSNP153 33..33 33 - - - 11309 RMVar_ID_11309 Human_SNP_ID_228576372 A-to-I Human chr5 - 38834683 38834683 38834683 TCTCTCTTTTTTTTTTTTCCTTTTTTTGAGACAGAGTCTAACATTGTTGCCCAGGCTGAGGTGGA TCTCTCTTTTTTTTTTTTCCTTTTTTTGAGACGGAGTCTAACATTGTTGCCCAGGCTGAGGTGGA T C OSMR-AS1 Ensembl:ENSG00000249740 lincRNA intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1386851141 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2931868,Human_RBP_ID_15447934 11310 RMVar_ID_11310 Human_SNP_ID_228607769 A-to-I Human chr5 - 38968523 38968523 38968523 ATGTTCCTAGTCTCAAAATTCTGGCCTCAAGCAGTCCTCCCACCTTGGCTTCCCAAAGGGCTTTT ATGTTCCTAGTCTCAAAATTCTGGCCTCAAGCGGTCCTCCCACCTTGGCTTCCCAAAGGGCTTTT T C RICTOR Ensembl:ENSG00000164327 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs547763039 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25896062 RMVar_hsa_circ_82788,RMVar_hsa_circ_120587,RMVar_hsa_circ_231127,RMVar_hsa_circ_231130,RMVar_hsa_circ_77295,RMVar_hsa_circ_87298,RMVar_hsa_circ_231138,RMVar_hsa_circ_115722,RMVar_hsa_circ_231139,RMVar_hsa_circ_231143,RMVar_hsa_circ_106302,RMVar_hsa_circ_231142,RMVar_hsa_circ_307399,RMVar_hsa_circ_231144,RMVar_hsa_circ_291975,RMVar_hsa_circ_231146 11311 RMVar_ID_11311 Human_SNP_ID_228607770 A-to-I Human chr5 - 38968523 38968523 38968523 ATGTTCCTAGTCTCAAAATTCTGGCCTCAAGCAGTCCTCCCACCTTGGCTTCCCAAAGGGCTTTT ATGTTCCTAGTCTCAAAATTCTGGCCTCAAGCCGTCCTCCCACCTTGGCTTCCCAAAGGGCTTTT T G RICTOR Ensembl:ENSG00000164327 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs547763039 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25896062 RMVar_hsa_circ_82788,RMVar_hsa_circ_120587,RMVar_hsa_circ_231127,RMVar_hsa_circ_231130,RMVar_hsa_circ_77295,RMVar_hsa_circ_87298,RMVar_hsa_circ_231138,RMVar_hsa_circ_115722,RMVar_hsa_circ_231139,RMVar_hsa_circ_231143,RMVar_hsa_circ_106302,RMVar_hsa_circ_231142,RMVar_hsa_circ_307399,RMVar_hsa_circ_231144,RMVar_hsa_circ_291975,RMVar_hsa_circ_231146 11312 RMVar_ID_11312 Human_SNP_ID_228607803 A-to-I Human chr5 - 38968707 38968707 38968707 TTAAGAGGCAGGGTCTTGCTGTCACCCAGGCTAGAGTGCAGTGGAATGATCATAGCTCACTGCAT TTAAGAGGCAGGGTCTTGCTGTCACCCAGGCTGGAGTGCAGTGGAATGATCATAGCTCACTGCAT T C RICTOR Ensembl:ENSG00000164327 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1319562337 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15448407 RMVar_hsa_circ_82788,RMVar_hsa_circ_120587,RMVar_hsa_circ_231127,RMVar_hsa_circ_231130,RMVar_hsa_circ_77295,RMVar_hsa_circ_87298,RMVar_hsa_circ_231138,RMVar_hsa_circ_115722,RMVar_hsa_circ_231139,RMVar_hsa_circ_231143,RMVar_hsa_circ_106302,RMVar_hsa_circ_231142,RMVar_hsa_circ_307399,RMVar_hsa_circ_231144,RMVar_hsa_circ_291975,RMVar_hsa_circ_231146 11313 RMVar_ID_11313 Human_SNP_ID_228611498 A-to-I Human chr5 - 38983878 38983878 38983878 TCACTGCAACCTCCGCCTCCTGGGTTCAGGCAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGA TCACTGCAACCTCCGCCTCCTGGGTTCAGGCAGTTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGA T C RICTOR Ensembl:ENSG00000164327 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1031781634 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82788,RMVar_hsa_circ_231130,RMVar_hsa_circ_32850,RMVar_hsa_circ_87298,RMVar_hsa_circ_115722,RMVar_hsa_circ_231139,RMVar_hsa_circ_231143,RMVar_hsa_circ_68628,RMVar_hsa_circ_340006,RMVar_hsa_circ_343136,RMVar_hsa_circ_306037,RMVar_hsa_circ_280535,RMVar_hsa_circ_231147,RMVar_hsa_circ_231148,RMVar_hsa_circ_285758,RMVar_hsa_circ_313907,RMVar_hsa_circ_337226,RMVar_hsa_circ_231154,RMVar_hsa_circ_34249,RMVar_hsa_circ_345822,RMVar_hsa_circ_299909,RMVar_hsa_circ_336989,RMVar_hsa_circ_231156 11314 RMVar_ID_11314 Human_SNP_ID_229059935 A-to-I Human chr5 - 40719347 40719347 40719347 CTGTTACAACACGGATGAACTTTAAAAACAATATGTTAAGTGAAAGAAACCAGACATAAAAGGCT CTGTTACAACACGGATGAACTTTAAAAACAATTTGTTAAGTGAAAGAAACCAGACATAAAAGGCT T A TTC33 Ensembl:ENSG00000113638 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1286685153 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_231175,RMVar_hsa_circ_85021,RMVar_hsa_circ_85898,RMVar_hsa_circ_231176 11315 RMVar_ID_11315 Human_SNP_ID_229059936 A-to-I Human chr5 - 40719347 40719347 40719347 CTGTTACAACACGGATGAACTTTAAAAACAATATGTTAAGTGAAAGAAACCAGACATAAAAGGCT CTGTTACAACACGGATGAACTTTAAAAACAATGTGTTAAGTGAAAGAAACCAGACATAAAAGGCT T C TTC33 Ensembl:ENSG00000113638 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1286685153 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_231175,RMVar_hsa_circ_85021,RMVar_hsa_circ_85898,RMVar_hsa_circ_231176 11316 RMVar_ID_11316 Human_SNP_ID_229059937 A-to-I Human chr5 - 40719349 40719349 40719349 GCCTGTTACAACACGGATGAACTTTAAAAACAATATGTTAAGTGAAAGAAACCAGACATAAAAGG GCCTGTTACAACACGGATGAACTTTAAAAACAGTATGTTAAGTGAAAGAAACCAGACATAAAAGG T C TTC33 Ensembl:ENSG00000113638 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334655188 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_231175,RMVar_hsa_circ_85021,RMVar_hsa_circ_85898,RMVar_hsa_circ_231176 11317 RMVar_ID_11317 Human_SNP_ID_229060143 A-to-I Human chr5 - 40720398 40720397 40720399 ATAGTACTTAGATAGGCATAATGTAGACATATAGATCAGTGGGATAGAACTGAAAGTACAGAAAT ATAGTACTTAGATAGGCATAATGTAGACATA__GATCAGTGGGATAGAACTGAAAGTACAGAAAT CTA C TTC33 Ensembl:ENSG00000113638 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1411109006 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_15449869 RMVar_hsa_circ_231175,RMVar_hsa_circ_85021,RMVar_hsa_circ_85898,RMVar_hsa_circ_231176 11318 RMVar_ID_11318 Human_SNP_ID_229061213 A-to-I Human chr5 - 40724246 40724246 40724246 GCTTTCTGTGACTGGCTTCTTTCACTTAGCATAATGTCCTCAAAGTCCCATCCATGTTGTGTATT GCTTTCTGTGACTGGCTTCTTTCACTTAGCATGATGTCCTCAAAGTCCCATCCATGTTGTGTATT T C TTC33 Ensembl:ENSG00000113638 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1003345247 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_231175,RMVar_hsa_circ_85021,RMVar_hsa_circ_85898,RMVar_hsa_circ_231176 11319 RMVar_ID_11319 Human_SNP_ID_229061467 A-to-I Human chr5 - 40725214 40725214 40725214 GGGAGGCTGAGGCAGAAGGATTGCTTGAGGCCAGGAGTTTGGACCAACCTGGGTAGCATGGCAAG GGGAGGCTGAGGCAGAAGGATTGCTTGAGGCCGGGAGTTTGGACCAACCTGGGTAGCATGGCAAG T C TTC33 Ensembl:ENSG00000113638 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1467580424 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_231175,RMVar_hsa_circ_85021,RMVar_hsa_circ_85898,RMVar_hsa_circ_231176 11320 RMVar_ID_11320 Human_SNP_ID_229065815 A-to-I Human chr5 - 40743698 40743698 40743698 GCGATCTTGGCTCACTGCAACCTCCTTCTCCTAGGTTTAAGCAATCCTCCCTGCCTCAGCCTCCC GCGATCTTGGCTCACTGCAACCTCCTTCTCCTGGGTTTAAGCAATCCTCCCTGCCTCAGCCTCCC T C TTC33 Ensembl:ENSG00000113638 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1363297250 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_305529,RMVar_hsa_circ_231177,RMVar_hsa_circ_378010 11321 RMVar_ID_11321 Human_SNP_ID_229070197 A-to-I Human chr5 - 40762017 40762017 40762017 CCACCACCTCAGCTTCCCAAAGTGGTGGGATTACAGGCGTGAGCCACCGCACCCGGCCTCCATAT CCACCACCTCAGCTTCCCAAAGTGGTGGGATTGCAGGCGTGAGCCACCGCACCCGGCCTCCATAT T C PRKAA1 Ensembl:ENSG00000132356 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs970319821 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1400333 RMVar_hsa_circ_231181 11322 RMVar_ID_11322 Human_SNP_ID_229070198 A-to-I Human chr5 - 40762029 40762029 40762029 TGACCGCGTGATCCACCACCTCAGCTTCCCAAAGTGGTGGGATTACAGGCGTGAGCCACCGCACC TGACCGCGTGATCCACCACCTCAGCTTCCCAAGGTGGTGGGATTACAGGCGTGAGCCACCGCACC T C PRKAA1 Ensembl:ENSG00000132356 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1039658224 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_231181 11323 RMVar_ID_11323 Human_SNP_ID_229070199 A-to-I Human chr5 - 40762030 40762030 40762030 CTGACCGCGTGATCCACCACCTCAGCTTCCCAAAGTGGTGGGATTACAGGCGTGAGCCACCGCAC CTGACCGCGTGATCCACCACCTCAGCTTCCCAGAGTGGTGGGATTACAGGCGTGAGCCACCGCAC T C PRKAA1 Ensembl:ENSG00000132356 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1361905163 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_231181 11324 RMVar_ID_11324 Human_SNP_ID_229070219 A-to-I Human chr5 - 40762088 40762088 40762088 TTTCGTATTTTTAGTGTAGACGGGGTTTCACTATGTTGCCCAGGCTGGTCTCGAACTCCTGACCG TTTCGTATTTTTAGTGTAGACGGGGTTTCACTGTGTTGCCCAGGCTGGTCTCGAACTCCTGACCG T C PRKAA1 Ensembl:ENSG00000132356 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749158711 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7439711,Human_RBP_ID_15450173 Human_miRNA_ID_1142089,Human_miRNA_ID_1159240 RMVar_hsa_circ_231181 11325 RMVar_ID_11325 Human_SNP_ID_229072241 A-to-I Human chr5 - 40770730 40770730 40770730 AAAATTAGCTGGGCATGGTGGTGCGTGCCTATAGTCCCCACTACCCTGGAGGCTGAGGCAGGAGA AAAATTAGCTGGGCATGGTGGTGCGTGCCTATGGTCCCCACTACCCTGGAGGCTGAGGCAGGAGA T C PRKAA1 Ensembl:ENSG00000132356 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1331345505 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4593,RMVar_hsa_circ_231183,RMVar_hsa_circ_287459,RMVar_hsa_circ_294897,RMVar_hsa_circ_231181,RMVar_hsa_circ_288348,RMVar_hsa_circ_231185,RMVar_hsa_circ_231186,RMVar_hsa_circ_231184,RMVar_hsa_circ_270305,RMVar_hsa_circ_73382,RMVar_hsa_circ_231182,RMVar_hsa_circ_17833,RMVar_hsa_circ_327406,RMVar_hsa_circ_231188,RMVar_hsa_circ_231189 11326 RMVar_ID_11326 Human_SNP_ID_229086355 A-to-I Human chr5 - 40825766 40825766 40825766 AGGAAGTTGAGACTGCAGTGAGCTGAGATTGCACCACTGCACTCCAGCCTCAGTGACAGCGAGAC AGGAAGTTGAGACTGCAGTGAGCTGAGATTGCGCCACTGCACTCCAGCCTCAGTGACAGCGAGAC T C RPL37 Ensembl:ENSG00000145592 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1406371373 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_642400,Human_RBP_ID_15450807,Human_RBP_ID_25897035 11327 RMVar_ID_11327 Human_SNP_ID_229086368 A-to-I Human chr5 - 40825798 40825798 40825798 CGAAGGCTGAGGCAGGAGGATCACCTGAGCCCAGGAAGTTGAGACTGCAGTGAGCTGAGATTGCA CGAAGGCTGAGGCAGGAGGATCACCTGAGCCCGGGAAGTTGAGACTGCAGTGAGCTGAGATTGCA T C RPL37 Ensembl:ENSG00000145592 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1016129812 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_642401 11328 RMVar_ID_11328 Human_SNP_ID_229086380 A-to-I Human chr5 - 40825844 40825844 40825844 AAAATTAGCCAGGTGCAGTGGCACACACCTGTAATCCCAGCTACTCCGAAGGCTGAGGCAGGAGG AAAATTAGCCAGGTGCAGTGGCACACACCTGTGATCCCAGCTACTCCGAAGGCTGAGGCAGGAGG T C RPL37 Ensembl:ENSG00000145592 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs926166830 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_642402 11329 RMVar_ID_11329 Human_SNP_ID_229086749 A-to-I Human chr5 - 40826906 40826906 40826906 AGGCATGGTGGTATGTGCCTGTAGTCCCAGCTACTCAGGGAGCTGAGGTGGAAGGATTGCTTGAG AGGCATGGTGGTATGTGCCTGTAGTCCCAGCTCCTCAGGGAGCTGAGGTGGAAGGATTGCTTGAG T G RPL37 Ensembl:ENSG00000145592 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1284554852 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_642429,Human_RBP_ID_788728,Human_RBP_ID_4831628,Human_RBP_ID_15450842 11330 RMVar_ID_11330 Human_SNP_ID_229086781 A-to-I Human chr5 - 40827005 40827005 40827005 GGAGGCTCAGAGGTGCCATTGGCTTGAGCCCAAGAGTTTGAGACCAGCCTGGGCAACCTGGTGAA GGAGGCTCAGAGGTGCCATTGGCTTGAGCCCAGGAGTTTGAGACCAGCCTGGGCAACCTGGTGAA T C RPL37 Ensembl:ENSG00000145592 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1174359963 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_642431,Human_RBP_ID_22301011 11331 RMVar_ID_11331 Human_SNP_ID_229086799 A-to-I Human chr5 - 40827060 40827060 40827060 AATTTAAAATACTCTGCCAGGTTCGGAGGTTCATGCTTGTCATCCCAGCACTTTGGGAGGCTCAG AATTTAAAATACTCTGCCAGGTTCGGAGGTTCGTGCTTGTCATCCCAGCACTTTGGGAGGCTCAG T C RPL37 Ensembl:ENSG00000145592 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs778530166 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_642433,Human_RBP_ID_7439996,Human_RBP_ID_8616127,Human_RBP_ID_15450848,Human_RBP_ID_17035325,Human_RBP_ID_17303896,Human_RBP_ID_17413717,Human_RBP_ID_18048498,Human_RBP_ID_18358652,Human_RBP_ID_24106365,Human_RBP_ID_26826240 11332 RMVar_ID_11332 Human_SNP_ID_229087686 A-to-I Human chr5 - 40829878 40829878 40829878 GTGAGGTGGGGAGTTCGAGACCAGCCTGACCAACATGGAGAAACCCCGTCTCTACTAAAAATACA GTGAGGTGGGGAGTTCGAGACCAGCCTGACCAGCATGGAGAAACCCCGTCTCTACTAAAAATACA T C RPL37 Ensembl:ENSG00000145592 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs977760771 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23045307 11333 RMVar_ID_11333 Human_SNP_ID_229087687 A-to-I Human chr5 - 40829878 40829878 40829878 GTGAGGTGGGGAGTTCGAGACCAGCCTGACCAACATGGAGAAACCCCGTCTCTACTAAAAATACA GTGAGGTGGGGAGTTCGAGACCAGCCTGACCACCATGGAGAAACCCCGTCTCTACTAAAAATACA T G RPL37 Ensembl:ENSG00000145592 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs977760771 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23045307 11334 RMVar_ID_11334 Human_SNP_ID_229087713 A-to-I Human chr5 - 40829948 40829948 40829948 GTGGCGGCCGGGTACGGTAGCTCACGTCCTATAGTCGCAGCACTTTGGGAGGCCAAGGTGGGCAG GTGGCGGCCGGGTACGGTAGCTCACGTCCTATGGTCGCAGCACTTTGGGAGGCCAAGGTGGGCAG T C RPL37 Ensembl:ENSG00000145592 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1182138948 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15451004,Human_RBP_ID_25897089 11335 RMVar_ID_11335 Human_SNP_ID_229087714 A-to-I Human chr5 - 40829950 40829950 40829950 CTGTGGCGGCCGGGTACGGTAGCTCACGTCCTATAGTCGCAGCACTTTGGGAGGCCAAGGTGGGC CTGTGGCGGCCGGGTACGGTAGCTCACGTCCTGTAGTCGCAGCACTTTGGGAGGCCAAGGTGGGC T C RPL37 Ensembl:ENSG00000145592 Protein coding 3'UTR GSE100210;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229 RNA-Seq:(High) rs1029613421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15451004 11336 RMVar_ID_11336 Human_SNP_ID_229087719 A-to-I Human chr5 - 40829962 40829961 40829962 GAAAGGTTGAATCTGTGGCGGCCGGGTACGGTAGCTCACGTCCTATAGTCGCAGCACTTTGGGAG GAAAGGTTGAATCTGTGGCGGCCGGGTACGGT_GCTCACGTCCTATAGTCGCAGCACTTTGGGAG CT C RPL37 Ensembl:ENSG00000145592 Protein coding 3'UTR GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs1237655413 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_15451005 11337 RMVar_ID_11337 Human_SNP_ID_229087720 A-to-I Human chr5 - 40829962 40829962 40829962 GAAAGGTTGAATCTGTGGCGGCCGGGTACGGTAGCTCACGTCCTATAGTCGCAGCACTTTGGGAG GAAAGGTTGAATCTGTGGCGGCCGGGTACGGTGGCTCACGTCCTATAGTCGCAGCACTTTGGGAG T C RPL37 Ensembl:ENSG00000145592 Protein coding 3'UTR GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs1355655226 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15451005 11338 RMVar_ID_11338 Human_SNP_ID_229087758 A-to-I Human chr5 - 40830088 40830088 40830088 CCTCCCTCCAGCCCCTACTTCCCTCCCATCTTAGTTCACAAAGTCAGGTTGATTTGCCCCCAGCT CCTCCCTCCAGCCCCTACTTCCCTCCCATCTTGGTTCACAAAGTCAGGTTGATTTGCCCCCAGCT T C RPL37 Ensembl:ENSG00000145592 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1478771038 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4831705,Human_RBP_ID_10206064,Human_RBP_ID_17090194,Human_RBP_ID_18048506,Human_RBP_ID_23045310 11339 RMVar_ID_11339 Human_SNP_ID_229087842 A-to-I Human chr5 - 40830363 40830363 40830363 GTTTCAAGTGATCCTCTCATCTTGGCCTCCCAAAGTGCTGGGATTACAGGGACGAGCCACCACAC GTTTCAAGTGATCCTCTCATCTTGGCCTCCCAGAGTGCTGGGATTACAGGGACGAGCCACCACAC T C RPL37 Ensembl:ENSG00000145592 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956158980 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1391580 11340 RMVar_ID_11340 Human_SNP_ID_229087846 A-to-I Human chr5 - 40830389 40830389 40830389 TTGCCCAGGCTGGTCTTGGACTCCTGGTTTCAAGTGATCCTCTCATCTTGGCCTCCCAAAGTGCT TTGCCCAGGCTGGTCTTGGACTCCTGGTTTCAGGTGATCCTCTCATCTTGGCCTCCCAAAGTGCT T C RPL37 Ensembl:ENSG00000145592 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1311333931 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1391580,Human_RBP_ID_17575389 Human_miRNA_ID_1039439 11341 RMVar_ID_11341 Human_SNP_ID_229087854 A-to-I Human chr5 - 40830415 40830415 40830415 TGCATTGGAGATGGAGTTAAACTATGTTGCCCAGGCTGGTCTTGGACTCCTGGTTTCAAGTGATC TGCATTGGAGATGGAGTTAAACTATGTTGCCCTGGCTGGTCTTGGACTCCTGGTTTCAAGTGATC T A RPL37 Ensembl:ENSG00000145592 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1040113069 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7440073,Human_RBP_ID_17575389,Human_RBP_ID_24106418 Human_miRNA_ID_1159242 11342 RMVar_ID_11342 Human_SNP_ID_229087855 A-to-I Human chr5 - 40830415 40830415 40830415 TGCATTGGAGATGGAGTTAAACTATGTTGCCCAGGCTGGTCTTGGACTCCTGGTTTCAAGTGATC TGCATTGGAGATGGAGTTAAACTATGTTGCCCGGGCTGGTCTTGGACTCCTGGTTTCAAGTGATC T C RPL37 Ensembl:ENSG00000145592 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1040113069 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7440073,Human_RBP_ID_17575389,Human_RBP_ID_24106418 Human_miRNA_ID_1159242 11343 RMVar_ID_11343 Human_SNP_ID_229087857 A-to-I Human chr5 - 40830424 40830424 40830424 AGTGGATCTTGCATTGGAGATGGAGTTAAACTATGTTGCCCAGGCTGGTCTTGGACTCCTGGTTT AGTGGATCTTGCATTGGAGATGGAGTTAAACTGTGTTGCCCAGGCTGGTCTTGGACTCCTGGTTT T C RPL37 Ensembl:ENSG00000145592 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982166092 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7440073,Human_RBP_ID_15451020,Human_RBP_ID_17575389,Human_RBP_ID_24106418 11344 RMVar_ID_11344 Human_SNP_ID_229087928 A-to-I Human chr5 - 40830625 40830625 40830625 GGGTGTGGTGGCATGTGCCTGTAGTCTTAGCTACTTGAGAGGCTGAGGCAGGAGAATCGCTTGAA GGGTGTGGTGGCATGTGCCTGTAGTCTTAGCTGCTTGAGAGGCTGAGGCAGGAGAATCGCTTGAA T C RPL37 Ensembl:ENSG00000145592 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1435566494 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8616144 11345 RMVar_ID_11345 Human_SNP_ID_229087931 A-to-I Human chr5 - 40830635 40830635 40830635 AAAATTAGCTGGGTGTGGTGGCATGTGCCTGTAGTCTTAGCTACTTGAGAGGCTGAGGCAGGAGA AAAATTAGCTGGGTGTGGTGGCATGTGCCTGTGGTCTTAGCTACTTGAGAGGCTGAGGCAGGAGA T C RPL37 Ensembl:ENSG00000145592 Protein coding 3'UTR GSE38233;GSE100210;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 24183664,29129909,30559470 RNA-Seq:(High) rs1482897922 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2933383,Human_RBP_ID_8616144,Human_RBP_ID_25941731 11346 RMVar_ID_11346 Human_SNP_ID_229087946 A-to-I Human chr5 - 40830675 40830675 40830675 CTGGCCCACATGGTGAGACCCCAACTCTACTAAAAATACAAAAATTAGCTGGGTGTGGTGGCATG CTGGCCCACATGGTGAGACCCCAACTCTACTAGAAATACAAAAATTAGCTGGGTGTGGTGGCATG T C RPL37 Ensembl:ENSG00000145592 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1468295243 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10237357,Human_RBP_ID_23045312 11347 RMVar_ID_11347 Human_SNP_ID_229088045 A-to-I Human chr5 - 40830996 40830996 40830996 CGTGATCCGCCGCCTCGGCCTCCCAAAGTGCTAGGATTACAGGCGTGAGCCACCACTCCCGGCTG CGTGATCCGCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCACTCCCGGCTG T C RPL37 Ensembl:ENSG00000145592 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1432612712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15451034 11348 RMVar_ID_11348 Human_SNP_ID_229088065 A-to-I Human chr5 - 40831037 40831037 40831037 GGGTTTCAACATGTTGACCAGGCTGGTCTCGAACTCGACCTCGTGATCCGCCGCCTCGGCCTCCC GGGTTTCAACATGTTGACCAGGCTGGTCTCGAGCTCGACCTCGTGATCCGCCGCCTCGGCCTCCC T C RPL37 Ensembl:ENSG00000145592 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1019891650 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17575639,Human_RBP_ID_23193695 11349 RMVar_ID_11349 Human_SNP_ID_229088107 A-to-I Human chr5 - 40831163 40831163 40831163 CTCCTGCCTCAGCCTTCTGAGTAGCTGGGACTACAGATGCACACCACCACACCTGGCTAATTTTT CTCCTGCCTCAGCCTTCTGAGTAGCTGGGACTGCAGATGCACACCACCACACCTGGCTAATTTTT T C RPL37 Ensembl:ENSG00000145592 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1187844757 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25897106 11350 RMVar_ID_11350 Human_SNP_ID_229088110 A-to-I Human chr5 - 40831173 40831173 40831173 TCAAGTGGTTCTCCTGCCTCAGCCTTCTGAGTAGCTGGGACTACAGATGCACACCACCACACCTG TCAAGTGGTTCTCCTGCCTCAGCCTTCTGAGTGGCTGGGACTACAGATGCACACCACCACACCTG T C RPL37 Ensembl:ENSG00000145592 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251789819 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2933386 11351 RMVar_ID_11351 Human_SNP_ID_229088123 A-to-I Human chr5 - 40831251 40831251 40831251 TGCCATTGCCTTTCTTGTTTACAGATAGTGCAATGGCGCAATCCTGGCTCACTGCAGCCTCTAAT TGCCATTGCCTTTCTTGTTTACAGATAGTGCAGTGGCGCAATCCTGGCTCACTGCAGCCTCTAAT T C RPL37 Ensembl:ENSG00000145592 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs747294509 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21088612,Human_RBP_ID_24506835,Human_RBP_ID_25941734 11352 RMVar_ID_11352 Human_SNP_ID_229089223 A-to-I Human chr5 - 40834563 40834563 40834563 GTCATCGTTTGGAAAGCGTCGCAATAAGACGCACACGTTGTGCCGCCGCTGTGGCTCTAAGGCCT GTCATCGTTTGGAAAGCGTCGCAATAAGACGCGCACGTTGTGCCGCCGCTGTGGCTCTAAGGCCT T C RPL37 Ensembl:ENSG00000145592 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1345039685 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_75605,Human_RBP_ID_642497,Human_RBP_ID_1660997,Human_RBP_ID_1995616,Human_RBP_ID_3770762,Human_RBP_ID_4831742,Human_RBP_ID_8616173,Human_RBP_ID_9177123,Human_RBP_ID_15451228,Human_RBP_ID_17530132,Human_RBP_ID_18842899,Human_RBP_ID_24106458,Human_RBP_ID_25897164,Human_RBP_ID_26527057 Human_Splice_Rec_646676,Human_Splice_Rec_646677,Human_Splice_Rec_646686,Human_Splice_Rec_646687,Human_Splice_Rec_646689,Human_Splice_Rec_646696,Human_Splice_Rec_646697,Human_Splice_Rec_646702,Human_Splice_Rec_646703 Human_miRNA_ID_2205791 RMVar_hsa_circ_86471,RMVar_hsa_circ_231194,RMVar_hsa_circ_326681,RMVar_hsa_circ_368655 11353 RMVar_ID_11353 Human_SNP_ID_229095864 A-to-I Human chr5 + 40859554 40859554 40859554 AAAGTCTGGGCTGGGAGTGGTGGCTCACGCCTATAATCCCAGCACTTTGGCAGGCCGAGGCGAGT AAAGTCTGGGCTGGGAGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGCAGGCCGAGGCGAGT A G CARD6 Ensembl:ENSG00000132357 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1271120735 Functional Loss SNV dbSNP153 33..33 33 - - - 11354 RMVar_ID_11354 Human_SNP_ID_229250794 A-to-I Human chr5 - 41456701 41456701 41456701 AGGGATCTCTCTAGGATTTCCTTTCTAAGGGCACTTACCTTATTCATAAGAGCTCCACCTTCAGG AGGGATCTCTCTAGGATTTCCTTTCTAAGGGCTCTTACCTTATTCATAAGAGCTCCACCTTCAGG T A PLCXD3 Ensembl:ENSG00000182836 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs746173247 Functional Loss SNV dbSNP153 33..33 33 - - - 11355 RMVar_ID_11355 Human_SNP_ID_229508781 A-to-I Human chr5 - 42465821 42465821 42465821 TAGACTGATTATTGACCGACCTATTCAAGGTCATGGTGGTCTTGGAAGAGGTCGAGAGGGCAGTG TAGACTGATTATTGACCGACCTATTCAAGGTCCTGGTGGTCTTGGAAGAGGTCGAGAGGGCAGTG T G SERBP1P6 Ensembl:ENSG00000248873 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs566754585 Functional Loss SNV dbSNP153 33..33 33 - - - 11356 RMVar_ID_11356 Human_SNP_ID_229640424 A-to-I Human chr5 - 42985300 42985300 42985300 ACAGTTGGGATGCAGTGGCACAATTGTAGCTCACTGTAATCTCTACCTCCTACACCTAAGGGAAC ACAGTTGGGATGCAGTGGCACAATTGTAGCTCGCTGTAATCTCTACCTCCTACACCTAAGGGAAC T C AC008875.3 Ensembl:ENSG00000287263 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1410768041 Functional Loss SNV dbSNP153 33..33 33 - - - 11357 RMVar_ID_11357 Human_SNP_ID_229642685 A-to-I Human chr5 - 42993102 42993102 42993102 CAGCCTGGTCAATATGATGAAACACCGCCTCTAGTAAAAATACAAAAATTATCCGGGCGTGGTGG CAGCCTGGTCAATATGATGAAACACCGCCTCTGGTAAAAATACAAAAATTATCCGGGCGTGGTGG T C AC008875.3 Ensembl:ENSG00000287263 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs959257021 Functional Loss SNV dbSNP153 33..33 33 - - - 11358 RMVar_ID_11358 Human_SNP_ID_229643454 A-to-I Human chr5 + 42995780 42995780 42995780 ACAAAAATTAGCCGGTGATGATGCATGCCTGCAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA ACAAAAATTAGCCGGTGATGATGCATGCCTGCGATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA A G AC008875.2 Ensembl:ENSG00000286656 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388650564 Functional Loss SNV dbSNP153 33..33 33 - - - 11359 RMVar_ID_11359 Human_SNP_ID_229643458 A-to-I Human chr5 + 42995794 42995794 42995794 GTGATGATGCATGCCTGCAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCTCTTGAACTCG GTGATGATGCATGCCTGCAATCCCAGCTACTCCGGAGGCTGAGGCAGGAGAATCTCTTGAACTCG A C AC008875.2 Ensembl:ENSG00000286656 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs938584975 Functional Loss SNV dbSNP153 33..33 33 - - - 11360 RMVar_ID_11360 Human_SNP_ID_229643459 A-to-I Human chr5 + 42995794 42995794 42995794 GTGATGATGCATGCCTGCAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCTCTTGAACTCG GTGATGATGCATGCCTGCAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCTCTTGAACTCG A G AC008875.2 Ensembl:ENSG00000286656 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs938584975 Functional Loss SNV dbSNP153 33..33 33 - - - 11361 RMVar_ID_11361 Human_SNP_ID_229643468 A-to-I Human chr5 + 42995832 42995832 42995832 CTGAGGCAGGAGAATCTCTTGAACTCGGAGGCAGAGGTTGCAGTGAGCTCAGATCGTGCCACCGT CTGAGGCAGGAGAATCTCTTGAACTCGGAGGCGGAGGTTGCAGTGAGCTCAGATCGTGCCACCGT A G AC008875.2 Ensembl:ENSG00000286656 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1240492532 Functional Loss SNV dbSNP153 33..33 33 - - - 11362 RMVar_ID_11362 Human_SNP_ID_229648410 A-to-I Human chr5 - 43014367 43014367 43014367 CCAAGGTGGTGGCATGCACCTTGCTGCCAGCTACTGTGGAGGCTGAGGTGAGAGGATTGTTTAAG CCAAGGTGGTGGCATGCACCTTGCTGCCAGCTGCTGTGGAGGCTGAGGTGAGAGGATTGTTTAAG T C AC025171.1 Ensembl:ENSG00000177738 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1387015309 Functional Loss SNV dbSNP153 33..33 33 - - - 11363 RMVar_ID_11363 Human_SNP_ID_229650646 A-to-I Human chr5 + 43023676 43023676 43023676 AAAATTAGCCAGAAGTGGTGGCGGGTGCCTGTAATCCTAGCTACTAGGGAGGCTGAGGCAAGAGA AAAATTAGCCAGAAGTGGTGGCGGGTGCCTGTTATCCTAGCTACTAGGGAGGCTGAGGCAAGAGA A T AC025171.3 Ensembl:ENSG00000251131 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1338854909 Functional Loss SNV dbSNP153 33..33 33 - - - 11364 RMVar_ID_11364 Human_SNP_ID_229650831 A-to-I Human chr5 + 43024378 43024378 43024378 TTTTGTATTTTTTGTAGACACCGTGTTTCGCCATGTTGCCCAGGCTGGTCTCAAACTCCTGAGCT TTTTGTATTTTTTGTAGACACCGTGTTTCGCCGTGTTGCCCAGGCTGGTCTCAAACTCCTGAGCT A G AC025171.3 Ensembl:ENSG00000251131 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264838410 Functional Loss SNV dbSNP153 33..33 33 - - - 11365 RMVar_ID_11365 Human_SNP_ID_229651378 A-to-I Human chr5 + 43026450 43026450 43026450 ATAATCACTGCTCACTTCAGCCTTAATCTCCTAGACTCAAGCAATCCTCCCACCTAAGCCTACCA ATAATCACTGCTCACTTCAGCCTTAATCTCCTTGACTCAAGCAATCCTCCCACCTAAGCCTACCA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1336805503 Functional Loss SNV dbSNP153 33..33 33 - - - 11366 RMVar_ID_11366 Human_SNP_ID_229651405 A-to-I Human chr5 + 43026544 43026544 43026544 CACTCAGAGAATTTTAAAAATTTTGTAGAGATAGAGTCTCCCTCTGCTGCCCAGGCTGATCTCAA CACTCAGAGAATTTTAAAAATTTTGTAGAGATGGAGTCTCCCTCTGCTGCCCAGGCTGATCTCAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1033557217 Functional Loss SNV dbSNP153 33..33 33 - - - 11367 RMVar_ID_11367 Human_SNP_ID_229652779 A-to-I Human chr5 - 43031642 43031642 43031642 TGGGGTTTCACCATGTGGGCCAGGCTGGTCTCAAACTCCTGACCTCAAATTATCCCTCCCTGCCC TGGGGTTTCACCATGTGGGCCAGGCTGGTCTCGAACTCCTGACCTCAAATTATCCCTCCCTGCCC T C AC025171.1 Ensembl:ENSG00000177738 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1172713605 Functional Loss SNV dbSNP153 33..33 33 - - - 11368 RMVar_ID_11368 Human_SNP_ID_229656650 A-to-I Human chr5 + 43043700 43043699 43043701 TAAATATAAATATATATTTTTATATATTATATAAAATATATAAATATATATTTATTTATATATTA TAAATATAAATATATATTTTTATATATTATAT__AATATATAAATATATATTTATTTATATATTA TAA T AC025171.2 Ensembl:ENSG00000215068 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1201367276 Functional Loss DEL dbSNP153 33..34 33 - - - 11369 RMVar_ID_11369 Human_SNP_ID_229656651 A-to-I Human chr5 + 43043700 43043700 43043700 TAAATATAAATATATATTTTTATATATTATATAAAATATATAAATATATATTTATTTATATATTA TAAATATAAATATATATTTTTATATATTATATTAAATATATAAATATATATTTATTTATATATTA A T AC025171.2 Ensembl:ENSG00000215068 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1249419867 Functional Loss SNV dbSNP153 33..33 33 - - - 11370 RMVar_ID_11370 Human_SNP_ID_229656659 A-to-I Human chr5 + 43043709 43043706 43043710 ATATATATTTTTATATATTATATAAAATATATAAATATATATTTATTTATATATTATATATAATA ATATATATTTTTATATATTATATAAAATAT____ATATATATTTATTTATATATTATATATAATA TATAA T AC025171.2 Ensembl:ENSG00000215068 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1404546432 Functional Loss DEL dbSNP153 31..34 33 - - - 11371 RMVar_ID_11371 Human_SNP_ID_229656661 A-to-I Human chr5 + 43043709 43043708 43043709 ATATATATTTTTATATATTATATAAAATATATAAATATATATTTATTTATATATTATATATAATA ATATATATTTTTATATATTATATAAAATATAT_AATATATATTTATTTATATATTATATATAATA TA T AC025171.2 Ensembl:ENSG00000215068 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1299409369 Functional Loss DEL dbSNP153 33..33 33 - - - 11372 RMVar_ID_11372 Human_SNP_ID_229658148 A-to-I Human chr5 + 43047530 43047530 43047530 GGGTGTGGTGGTGCATGCCTATAATCCCAGCTACACAGAGGTTGAGGCACGAGAATTGTTTCAAC GGGTGTGGTGGTGCATGCCTATAATCCCAGCTGCACAGAGGTTGAGGCACGAGAATTGTTTCAAC A G AC025171.2 Ensembl:ENSG00000215068 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223942260 Functional Loss SNV dbSNP153 33..33 33 - - - 11373 RMVar_ID_11373 Human_SNP_ID_229659211 A-to-I Human chr5 + 43052235 43052235 43052235 AGGAATGTGCCACCACACCTGGCTAATTTTGTATTTTTAGTAGAGACAGGGTTTCTCCATGTTGG AGGAATGTGCCACCACACCTGGCTAATTTTGTGTTTTTAGTAGAGACAGGGTTTCTCCATGTTGG A G AC025171.2 Ensembl:ENSG00000215068 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs528845370 Functional Loss SNV dbSNP153 33..33 33 - - - 11374 RMVar_ID_11374 Human_SNP_ID_229663735 A-to-I Human chr5 + 43069368 43069368 43069368 TCGGCTCACTGCAACATCCACCTCCCAGGTTCAAGTTATTCTCCTGCCTCAGCTCCCAAGCAGCC TCGGCTCACTGCAACATCCACCTCCCAGGTTCGAGTTATTCTCCTGCCTCAGCTCCCAAGCAGCC A G ZNF131 Ensembl:ENSG00000172262 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1464720762 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_231238 11375 RMVar_ID_11375 Human_SNP_ID_229663922 A-to-I Human chr5 + 43070028 43070016 43070028 GCGCCATTGCACTCCAGCCTGAGCGATAGAGCAAGACCCTGTCTCAAAAAAAAAAAAAAAAAACA GCGCCATTGCACTCCAGCCTG____________AGACCCTGTCTCAAAAAAAAAAAAAAAAAACA GAGCGATAGAGCA G ZNF131 Ensembl:ENSG00000172262 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1190970794 Functional Loss DEL dbSNP153 22..33 33 - - - RMVar_hsa_circ_231238 11376 RMVar_ID_11376 Human_SNP_ID_229664303 A-to-I Human chr5 + 43071804 43071803 43071805 ATGGAAATATGAATGATTTTTTTTTTTGAGACAGAGTCTCTCTCTGTCGCCCAGGCTGGAATGCA ATGGAAATATGAATGATTTTTTTTTTTGAGAC__AGTCTCTCTCTGTCGCCCAGGCTGGAATGCA CAG C ZNF131 Ensembl:ENSG00000172262 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1236783023 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_231238 11377 RMVar_ID_11377 Human_SNP_ID_229664478 A-to-I Human chr5 + 43072398 43072398 43072398 TCACTCGTACTGCTGCCCAGGCTATATAGTGCAATGGCACCATCTTGGCTCACCACAACCTCCGC TCACTCGTACTGCTGCCCAGGCTATATAGTGCGATGGCACCATCTTGGCTCACCACAACCTCCGC A G ZNF131 Ensembl:ENSG00000172262 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1400697267 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_231238 11378 RMVar_ID_11378 Human_SNP_ID_229665490 A-to-I Human chr5 + 43076620 43076620 43076620 GGGAGACCGAGGCAGGTGGATCACCTGAAGTCAAGAGTTCGAGACCAGCCTGGCCAACATGGTGA GGGAGACCGAGGCAGGTGGATCACCTGAAGTCGAGAGTTCGAGACCAGCCTGGCCAACATGGTGA A G ZNF131 Ensembl:ENSG00000172262 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1138083 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_231238 11379 RMVar_ID_11379 Human_SNP_ID_229665549 A-to-I Human chr5 + 43076796 43076796 43076796 TTGAAGCCAGGAGGTAGAGGTTGCAATGAGCCAAGATCGTACCACTGCACTCCAGCCTGCGTGAT TTGAAGCCAGGAGGTAGAGGTTGCAATGAGCCGAGATCGTACCACTGCACTCCAGCCTGCGTGAT A G ZNF131 Ensembl:ENSG00000172262 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs112044936 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_231238 11380 RMVar_ID_11380 Human_SNP_ID_229666023 A-to-I Human chr5 + 43078627 43078627 43078627 GAAAATTAGCCGGACGAGGTGGCGGGCCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAAGAGA GAAAATTAGCCGGACGAGGTGGCGGGCCCTGTGGTCCCAGCTACTCGGGAGGCTGAGGCAAGAGA A G ZNF131 Ensembl:ENSG00000172262 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1438501256 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_231238 11381 RMVar_ID_11381 Human_SNP_ID_229669573 A-to-I Human chr5 + 43090303 43090303 43090303 ATAGTTCACTGCAGCCTAGACCTCCTGGGCTCAAGCAGTCCTCTCACTTCAGCCTCCTGAGTAGC ATAGTTCACTGCAGCCTAGACCTCCTGGGCTCCAGCAGTCCTCTCACTTCAGCCTCCTGAGTAGC A C ZNF131 Ensembl:ENSG00000172262 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1161554574 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_231238 11382 RMVar_ID_11382 Human_SNP_ID_229678496 A-to-I Human chr5 + 43125393 43125393 43125393 CGTGATCAGGCTGGTCTCGAATTCCCCACCTCAGGTGATCCACCCGCCTCTTCCTCCCAAAGTGC CGTGATCAGGCTGGTCTCGAATTCCCCACCTCCGGTGATCCACCCGCCTCTTCCTCCCAAAGTGC A C ZNF131 Ensembl:ENSG00000172262 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1018884318 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17575643 RMVar_hsa_circ_231242,RMVar_hsa_circ_292127,RMVar_hsa_circ_322977,RMVar_hsa_circ_355952,RMVar_hsa_circ_287321,RMVar_hsa_circ_231241,RMVar_hsa_circ_320208,RMVar_hsa_circ_288229 11383 RMVar_ID_11383 Human_SNP_ID_229678497 A-to-I Human chr5 + 43125393 43125393 43125393 CGTGATCAGGCTGGTCTCGAATTCCCCACCTCAGGTGATCCACCCGCCTCTTCCTCCCAAAGTGC CGTGATCAGGCTGGTCTCGAATTCCCCACCTCGGGTGATCCACCCGCCTCTTCCTCCCAAAGTGC A G ZNF131 Ensembl:ENSG00000172262 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1018884318 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17575643 RMVar_hsa_circ_231242,RMVar_hsa_circ_292127,RMVar_hsa_circ_322977,RMVar_hsa_circ_355952,RMVar_hsa_circ_287321,RMVar_hsa_circ_231241,RMVar_hsa_circ_320208,RMVar_hsa_circ_288229 11384 RMVar_ID_11384 Human_SNP_ID_229678501 A-to-I Human chr5 + 43125402 43125402 43125402 GCTGGTCTCGAATTCCCCACCTCAGGTGATCCACCCGCCTCTTCCTCCCAAAGTGCTGGGATTAC GCTGGTCTCGAATTCCCCACCTCAGGTGATCCCCCCGCCTCTTCCTCCCAAAGTGCTGGGATTAC A C ZNF131 Ensembl:ENSG00000172262 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs955902767 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17575643 RMVar_hsa_circ_231242,RMVar_hsa_circ_292127,RMVar_hsa_circ_322977,RMVar_hsa_circ_355952,RMVar_hsa_circ_287321,RMVar_hsa_circ_231241,RMVar_hsa_circ_320208,RMVar_hsa_circ_288229 11385 RMVar_ID_11385 Human_SNP_ID_229679666 A-to-I Human chr5 + 43129216 43129216 43129216 CTTCAGCCTCCCAAAGTGCTGGTATTGCAGGCATGAGCCACCATGCCCAGCCTAGTTTTTGTATT CTTCAGCCTCCCAAAGTGCTGGTATTGCAGGCCTGAGCCACCATGCCCAGCCTAGTTTTTGTATT A C ZNF131 Ensembl:ENSG00000172262 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1451921006 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_231242,RMVar_hsa_circ_292127,RMVar_hsa_circ_322977,RMVar_hsa_circ_355952,RMVar_hsa_circ_287321,RMVar_hsa_circ_231241,RMVar_hsa_circ_320208,RMVar_hsa_circ_288229 11386 RMVar_ID_11386 Human_SNP_ID_229679667 A-to-I Human chr5 + 43129216 43129216 43129216 CTTCAGCCTCCCAAAGTGCTGGTATTGCAGGCATGAGCCACCATGCCCAGCCTAGTTTTTGTATT CTTCAGCCTCCCAAAGTGCTGGTATTGCAGGCGTGAGCCACCATGCCCAGCCTAGTTTTTGTATT A G ZNF131 Ensembl:ENSG00000172262 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1451921006 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_231242,RMVar_hsa_circ_292127,RMVar_hsa_circ_322977,RMVar_hsa_circ_355952,RMVar_hsa_circ_287321,RMVar_hsa_circ_231241,RMVar_hsa_circ_320208,RMVar_hsa_circ_288229 11387 RMVar_ID_11387 Human_SNP_ID_229679910 A-to-I Human chr5 + 43130125 43130125 43130125 GTCTCTACTGAAAATACAAAAATTAGCCGGACATGGCAGCGCGTGCCTGTAGTCCCAGCTACTGG GTCTCTACTGAAAATACAAAAATTAGCCGGACGTGGCAGCGCGTGCCTGTAGTCCCAGCTACTGG A G ZNF131 Ensembl:ENSG00000172262 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1191226592 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15452780 RMVar_hsa_circ_231242,RMVar_hsa_circ_292127,RMVar_hsa_circ_322977,RMVar_hsa_circ_355952,RMVar_hsa_circ_287321,RMVar_hsa_circ_231241,RMVar_hsa_circ_320208,RMVar_hsa_circ_288229 11388 RMVar_ID_11388 Human_SNP_ID_229681463 A-to-I Human chr5 + 43134960 43134960 43134960 CCTCAGGTGATCCATCCACCTCAGCCTCCGAAAATGTTGGATTGCAGGCATGAGCCACCGCGCCC CCTCAGGTGATCCATCCACCTCAGCCTCCGAATATGTTGGATTGCAGGCATGAGCCACCGCGCCC A T ZNF131 Ensembl:ENSG00000172262 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1414530149 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15452899,Human_RBP_ID_25897643 RMVar_hsa_circ_231242,RMVar_hsa_circ_292127,RMVar_hsa_circ_322977,RMVar_hsa_circ_355952,RMVar_hsa_circ_287321,RMVar_hsa_circ_231241,RMVar_hsa_circ_320208,RMVar_hsa_circ_288229 11389 RMVar_ID_11389 Human_SNP_ID_229681467 A-to-I Human chr5 + 43134977 43134977 43134977 ACCTCAGCCTCCGAAAATGTTGGATTGCAGGCATGAGCCACCGCGCCCGGCCATCAGTTACATTT ACCTCAGCCTCCGAAAATGTTGGATTGCAGGCCTGAGCCACCGCGCCCGGCCATCAGTTACATTT A C ZNF131 Ensembl:ENSG00000172262 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs575194647 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15452899 RMVar_hsa_circ_231242,RMVar_hsa_circ_292127,RMVar_hsa_circ_322977,RMVar_hsa_circ_355952,RMVar_hsa_circ_287321,RMVar_hsa_circ_231241,RMVar_hsa_circ_320208,RMVar_hsa_circ_288229 11390 RMVar_ID_11390 Human_SNP_ID_229681468 A-to-I Human chr5 + 43134977 43134977 43134977 ACCTCAGCCTCCGAAAATGTTGGATTGCAGGCATGAGCCACCGCGCCCGGCCATCAGTTACATTT ACCTCAGCCTCCGAAAATGTTGGATTGCAGGCGTGAGCCACCGCGCCCGGCCATCAGTTACATTT A G ZNF131 Ensembl:ENSG00000172262 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs575194647 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15452899 RMVar_hsa_circ_231242,RMVar_hsa_circ_292127,RMVar_hsa_circ_322977,RMVar_hsa_circ_355952,RMVar_hsa_circ_287321,RMVar_hsa_circ_231241,RMVar_hsa_circ_320208,RMVar_hsa_circ_288229 11391 RMVar_ID_11391 Human_SNP_ID_229681747 A-to-I Human chr5 + 43135860 43135860 43135860 GAACTGCTTGCCAGGTGCAGTGGCTCACGCCTATAGTCCCAGCACTTTGGGAGGCCGAGGCGGGC GAACTGCTTGCCAGGTGCAGTGGCTCACGCCTGTAGTCCCAGCACTTTGGGAGGCCGAGGCGGGC A G ZNF131 Ensembl:ENSG00000172262 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355343337 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15452906 RMVar_hsa_circ_231242,RMVar_hsa_circ_292127,RMVar_hsa_circ_322977,RMVar_hsa_circ_355952,RMVar_hsa_circ_287321,RMVar_hsa_circ_231241,RMVar_hsa_circ_320208,RMVar_hsa_circ_288229 11392 RMVar_ID_11392 Human_SNP_ID_229681784 A-to-I Human chr5 + 43135994 43135994 43135994 AAAATTAGGTGGGTATGGTGGTGCGTGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGAAGGAGA AAAATTAGGTGGGTATGGTGGTGCGTGCCTGTGGTCCCAGCTACTTGGGAGGCTGAGGAAGGAGA A G ZNF131 Ensembl:ENSG00000172262 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1354176726 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_231242,RMVar_hsa_circ_292127,RMVar_hsa_circ_322977,RMVar_hsa_circ_355952,RMVar_hsa_circ_287321,RMVar_hsa_circ_231241,RMVar_hsa_circ_320208,RMVar_hsa_circ_288229 11393 RMVar_ID_11393 Human_SNP_ID_229683302 A-to-I Human chr5 + 43141598 43141598 43141598 TGAGACCAGCCTGGGCACCATGGTGAAACGCCAACTCTATGAAAAATACAAAAATTAGCTGGCAC TGAGACCAGCCTGGGCACCATGGTGAAACGCCGACTCTATGAAAAATACAAAAATTAGCTGGCAC A G ZNF131 Ensembl:ENSG00000172262 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900258380 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_231242,RMVar_hsa_circ_322977,RMVar_hsa_circ_355952,RMVar_hsa_circ_287321,RMVar_hsa_circ_231243,RMVar_hsa_circ_295978,RMVar_hsa_circ_320208 11394 RMVar_ID_11394 Human_SNP_ID_229683307 A-to-I Human chr5 + 43141622 43141622 43141622 GAAACGCCAACTCTATGAAAAATACAAAAATTAGCTGGCACTGTGGCGTGCAACTGTAGTCCCAG GAAACGCCAACTCTATGAAAAATACAAAAATTGGCTGGCACTGTGGCGTGCAACTGTAGTCCCAG A G ZNF131 Ensembl:ENSG00000172262 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs771859401 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_231242,RMVar_hsa_circ_322977,RMVar_hsa_circ_355952,RMVar_hsa_circ_287321,RMVar_hsa_circ_231243,RMVar_hsa_circ_295978,RMVar_hsa_circ_320208 11395 RMVar_ID_11395 Human_SNP_ID_229683314 A-to-I Human chr5 + 43141641 43141641 43141641 AAATACAAAAATTAGCTGGCACTGTGGCGTGCAACTGTAGTCCCAGGTACTCAGGAGACTGAGGT AAATACAAAAATTAGCTGGCACTGTGGCGTGCCACTGTAGTCCCAGGTACTCAGGAGACTGAGGT A C ZNF131 Ensembl:ENSG00000172262 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs772999005 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_231242,RMVar_hsa_circ_322977,RMVar_hsa_circ_355952,RMVar_hsa_circ_287321,RMVar_hsa_circ_231243,RMVar_hsa_circ_295978,RMVar_hsa_circ_320208 11396 RMVar_ID_11396 Human_SNP_ID_229683678 A-to-I Human chr5 + 43142791 43142790 43142792 TCAGCTCACTGCAGCTTCAACTTCCCGGCCTCAAGAGATCCTCCCACCTTAGCCTCCCAAGTAGC TCAGCTCACTGCAGCTTCAACTTCCCGGCCTC__GAGATCCTCCCACCTTAGCCTCCCAAGTAGC CAA C ZNF131 Ensembl:ENSG00000172262 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs901934828 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_231242,RMVar_hsa_circ_322977,RMVar_hsa_circ_355952,RMVar_hsa_circ_287321,RMVar_hsa_circ_231243,RMVar_hsa_circ_295978,RMVar_hsa_circ_320208 11397 RMVar_ID_11397 Human_SNP_ID_229683702 A-to-I Human chr5 + 43142876 43142876 43142876 ACCATGCCTGGCTAATTTTTGTATTTCTTTGTAGAGACAGGATTTCACCATGTTGCCCAGGCTAC ACCATGCCTGGCTAATTTTTGTATTTCTTTGTGGAGACAGGATTTCACCATGTTGCCCAGGCTAC A G ZNF131 Ensembl:ENSG00000172262 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1466144523 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15452968 RMVar_hsa_circ_231242,RMVar_hsa_circ_322977,RMVar_hsa_circ_355952,RMVar_hsa_circ_287321,RMVar_hsa_circ_231243,RMVar_hsa_circ_295978,RMVar_hsa_circ_320208 11398 RMVar_ID_11398 Human_SNP_ID_229686043 A-to-I Human chr5 + 43150681 43150681 43150681 GGGCACGGTGACACATGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATTGCTGAGG GGGCACGGTGACACATGCCTGTAATCCCAGCTGCTCAGGAGGCTGAGGCAGGAGAATTGCTGAGG A G ZNF131 Ensembl:ENSG00000172262 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1320647257 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_231242,RMVar_hsa_circ_322977,RMVar_hsa_circ_355952,RMVar_hsa_circ_287321,RMVar_hsa_circ_231243,RMVar_hsa_circ_295978,RMVar_hsa_circ_320208 11399 RMVar_ID_11399 Human_SNP_ID_229686044 A-to-I Human chr5 + 43150685 43150685 43150685 ACGGTGACACATGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATTGCTGAGGCTGC ACGGTGACACATGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCTGAGGCTGC A G ZNF131 Ensembl:ENSG00000172262 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs939156932 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_231242,RMVar_hsa_circ_322977,RMVar_hsa_circ_355952,RMVar_hsa_circ_287321,RMVar_hsa_circ_231243,RMVar_hsa_circ_295978,RMVar_hsa_circ_320208 11400 RMVar_ID_11400 Human_SNP_ID_229686415 A-to-I Human chr5 + 43152089 43152089 43152089 GTGCAGTGACATGATCTTGGCTCACTGCCTCTACCTCCCAGGTTCAAGTGATTCTCCTGCCTCAG GTGCAGTGACATGATCTTGGCTCACTGCCTCTCCCTCCCAGGTTCAAGTGATTCTCCTGCCTCAG A C ZNF131 Ensembl:ENSG00000172262 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs921321998 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_231242,RMVar_hsa_circ_322977,RMVar_hsa_circ_355952,RMVar_hsa_circ_287321,RMVar_hsa_circ_231243,RMVar_hsa_circ_295978,RMVar_hsa_circ_320208 11401 RMVar_ID_11401 Human_SNP_ID_229686615 A-to-I Human chr5 + 43152844 43152844 43152844 GTTCTCCAGGCTGTTCTTAAACTCCCGGACTCAAGCGATCCTCCCGCCTCAGCCTCCCAAAGTGC GTTCTCCAGGCTGTTCTTAAACTCCCGGACTCGAGCGATCCTCCCGCCTCAGCCTCCCAAAGTGC A G ZNF131 Ensembl:ENSG00000172262 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs564569534 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_231242,RMVar_hsa_circ_322977,RMVar_hsa_circ_355952,RMVar_hsa_circ_287321,RMVar_hsa_circ_231243,RMVar_hsa_circ_295978,RMVar_hsa_circ_320208 11402 RMVar_ID_11402 Human_SNP_ID_229698519 A-to-I Human chr5 + 43195539 43195539 43195539 AAAATTAGCTGGGTGTGGTGGTGCATGCCTGTAGTCCCAGCTACTGGGGAGACTGAGGGAGGAGG AAAATTAGCTGGGTGTGGTGGTGCATGCCTGTGGTCCCAGCTACTGGGGAGACTGAGGGAGGAGG A G NIM1K Ensembl:ENSG00000177453 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1380978964 Functional Loss SNV dbSNP153 33..33 33 - - - 11403 RMVar_ID_11403 Human_SNP_ID_229706095 A-to-I Human chr5 + 43223018 43223018 43223018 AAAATTAGCCTGGCGTGGTGGTGCATGCCTGTAATCCCAGCTACTCCGGAGGCTGAGGCAGGAGA AAAATTAGCCTGGCGTGGTGGTGCATGCCTGTGATCCCAGCTACTCCGGAGGCTGAGGCAGGAGA A G NIM1K Ensembl:ENSG00000177453 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1259352893 Functional Loss SNV dbSNP153 33..33 33 - - - 11404 RMVar_ID_11404 Human_SNP_ID_229706097 A-to-I Human chr5 + 43223028 43223028 43223028 TGGCGTGGTGGTGCATGCCTGTAATCCCAGCTACTCCGGAGGCTGAGGCAGGAGAATCGCTTGAA TGGCGTGGTGGTGCATGCCTGTAATCCCAGCTGCTCCGGAGGCTGAGGCAGGAGAATCGCTTGAA A G NIM1K Ensembl:ENSG00000177453 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs958355122 Functional Loss SNV dbSNP153 33..33 33 - - - 11405 RMVar_ID_11405 Human_SNP_ID_229724754 A-to-I Human chr5 + 43291186 43291186 43291186 CAGCTGCTTCAGGTTCTGCTGCTGTGGCAGGGAGTCTTGGTACTTTCTTGGCAGGGCTTGGAATA CAGCTGCTTCAGGTTCTGCTGCTGTGGCAGGGGGTCTTGGTACTTTCTTGGCAGGGCTTGGAATA A G RF00017-1784 RNACentral:URS0000904F64 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs202048838 Functional Loss SNV dbSNP153 33..33 33 - - - 11406 RMVar_ID_11406 Human_SNP_ID_229747661 A-to-I Human chr5 - 43380115 43380114 43380116 TTTGTTGTTGTTTGGTTGTTTTTTTTTGAGACAGAGTCTCACTCTGTTGCCCAGGCTGGAGTGCA TTTGTTGTTGTTTGGTTGTTTTTTTTTGAGA__GAGTCTCACTCTGTTGCCCAGGCTGGAGTGCA CTG C CCL28 Ensembl:ENSG00000151882 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1205579946 Functional Loss DEL dbSNP153 32..33 33 - - - 11407 RMVar_ID_11407 Human_SNP_ID_229747784 A-to-I Human chr5 - 43380680 43380680 43380680 CTCCCACCTCAGCCTCCCGAGTATCTGGGATCAAGGTGCATACCCACCACACCTGGCTAATTTTG CTCCCACCTCAGCCTCCCGAGTATCTGGGATCGAGGTGCATACCCACCACACCTGGCTAATTTTG T C CCL28 Ensembl:ENSG00000151882 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1169474958 Functional Loss SNV dbSNP153 33..33 33 - - - 11408 RMVar_ID_11408 Human_SNP_ID_229747791 A-to-I Human chr5 - 43380715 43380715 43380715 TCACTGAAGCCTCAACTTCTAGGGCTCAAGCAATCCTCCCACCTCAGCCTCCCGAGTATCTGGGA TCACTGAAGCCTCAACTTCTAGGGCTCAAGCACTCCTCCCACCTCAGCCTCCCGAGTATCTGGGA T G CCL28 Ensembl:ENSG00000151882 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs977002471 Functional Loss SNV dbSNP153 33..33 33 - - - 11409 RMVar_ID_11409 Human_SNP_ID_229747948 A-to-I Human chr5 - 43381500 43381500 43381500 AAAAAATTGGCCCGGCATGGTAGTACTTGCCTATAATCCCAGCCACATGGGAGGCTGAGGTGGGA AAAAAATTGGCCCGGCATGGTAGTACTTGCCTGTAATCCCAGCCACATGGGAGGCTGAGGTGGGA T C CCL28 Ensembl:ENSG00000151882 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1046014100 Functional Loss SNV dbSNP153 33..33 33 - - - 11410 RMVar_ID_11410 Human_SNP_ID_229747982 A-to-I Human chr5 - 43381624 43381624 43381624 TGGGTATGGTGGTTCACACCTTTTATCCCAGCACTTCGGGAGGCTGAGGCAGGAGGATCACTTGA TGGGTATGGTGGTTCACACCTTTTATCCCAGCGCTTCGGGAGGCTGAGGCAGGAGGATCACTTGA T C CCL28 Ensembl:ENSG00000151882 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1353212020 Functional Loss SNV dbSNP153 33..33 33 - - - 11411 RMVar_ID_11411 Human_SNP_ID_229789234 A-to-I Human chr5 - 43544112 43544112 43544112 AAAGATGGGGGCTTTGTTTTGTCACCCAGACTAGAGTGCAGTGGCGTGACCACAGCTCACTGCAG AAAGATGGGGGCTTTGTTTTGTCACCCAGACTGGAGTGCAGTGGCGTGACCACAGCTCACTGCAG T C PAIP1 Ensembl:ENSG00000172239 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947558917 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_314900,RMVar_hsa_circ_231269 11412 RMVar_ID_11412 Human_SNP_ID_229789962 A-to-I Human chr5 - 43546991 43546991 43546991 TCTCCCAGGCTGGAGTGCAGTGGCGCAGTCTCAGCTCCCTGCGACCTCCGTCTCCCGGGTTCAAG TCTCCCAGGCTGGAGTGCAGTGGCGCAGTCTCGGCTCCCTGCGACCTCCGTCTCCCGGGTTCAAG T C PAIP1 Ensembl:ENSG00000172239 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs918404978 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_314900,RMVar_hsa_circ_231269 11413 RMVar_ID_11413 Human_SNP_ID_229796509 A-to-I Human chr5 - 43574171 43574171 43574171 GGAATTAGCTGGGCATGATGGTACACACTTGTAGTCCCAGCTACTTGGGGGACTGAGATGGGAAA GGAATTAGCTGGGCATGATGGTACACACTTGTCGTCCCAGCTACTTGGGGGACTGAGATGGGAAA T G NNT-AS1 Ensembl:ENSG00000248092 lincRNA exon GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1291099978 Functional Loss SNV dbSNP153 33..33 33 - - - 11414 RMVar_ID_11414 Human_SNP_ID_229796859 A-to-I Human chr5 - 43575702 43575702 43575702 GGGCATGGTGGCATGTGTCTGGAATCCCTGCTACTCAGGAGGCTGAGGCAAGAGGATCACTTGGA GGGCATGGTGGCATGTGTCTGGAATCCCTGCTCCTCAGGAGGCTGAGGCAAGAGGATCACTTGGA T G NNT-AS1 Ensembl:ENSG00000248092 lincRNA exon GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1217033980 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27516103 11415 RMVar_ID_11415 Human_SNP_ID_229796975 A-to-I Human chr5 - 43576227 43576227 43576227 TTCCTGGGCTCAAGCAATGTCCTCATCCTCCTACCTCAGCCTCTCAAGTAGCTGCTATTACAGGC TTCCTGGGCTCAAGCAATGTCCTCATCCTCCTTCCTCAGCCTCTCAAGTAGCTGCTATTACAGGC T A NNT-AS1 Ensembl:ENSG00000248092 lincRNA intron GSE100210;GSE99789;GSE107867;GSE123020:GSM3490829,GSM3490830,GSM3490831 HepG2 cell line;esophageal squamous carcinoma cells,EC109;ASD brains,cerebellum;esophageal squamous carcinoma cells,EC109 cell line - 29129909,29796672,30559470,32596459 RNA-Seq:(High) rs1331121258 Functional Loss SNV dbSNP153 33..33 33 - - - 11416 RMVar_ID_11416 Human_SNP_ID_229796991 A-to-I Human chr5 - 43576296 43576296 43576296 AGACTGGGTCTTAATCTGTTGTCCAGGCTGGAATGCAGTCACACAATCACAGCTCACTGCAGCCT AGACTGGGTCTTAATCTGTTGTCCAGGCTGGAGTGCAGTCACACAATCACAGCTCACTGCAGCCT T C NNT-AS1 Ensembl:ENSG00000248092 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1354228404 Functional Loss SNV dbSNP153 33..33 33 - - - 11417 RMVar_ID_11417 Human_SNP_ID_229798995 A-to-I Human chr5 - 43582352 43582351 43582352 GTATGTTAATAAATTTCTGTGCCATTTCTCCTATTAAGCTGCCTTTTATCAGTTGATTTTTCAGT GTATGTTAATAAATTTCTGTGCCATTTCTCCT_TTAAGCTGCCTTTTATCAGTTGATTTTTCAGT AT A NNT-AS1 Ensembl:ENSG00000248092 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1561248406 Functional Loss DEL dbSNP153 33..33 33 - - - 11418 RMVar_ID_11418 Human_SNP_ID_229798996 A-to-I Human chr5 - 43582352 43582352 43582352 GTATGTTAATAAATTTCTGTGCCATTTCTCCTATTAAGCTGCCTTTTATCAGTTGATTTTTCAGT GTATGTTAATAAATTTCTGTGCCATTTCTCCTGTTAAGCTGCCTTTTATCAGTTGATTTTTCAGT T C NNT-AS1 Ensembl:ENSG00000248092 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444329658 Functional Loss SNV dbSNP153 33..33 33 - - - 11419 RMVar_ID_11419 Human_SNP_ID_229799626 A-to-I Human chr5 - 43585170 43585170 43585170 ATAATAACAAAAGAAAAAATGCAGCCAGGCGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGG ATAATAACAAAAGAAAAAATGCAGCCAGGCGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGG T C NNT-AS1 Ensembl:ENSG00000248092 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1245818752 Functional Loss SNV dbSNP153 33..33 33 - - - 11420 RMVar_ID_11420 Human_SNP_ID_229799627 A-to-I Human chr5 - 43585170 43585170 43585170 ATAATAACAAAAGAAAAAATGCAGCCAGGCGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGG ATAATAACAAAAGAAAAAATGCAGCCAGGCGCCGTGGCTCACACCTGTAATCCCAGCACTTTGGG T G NNT-AS1 Ensembl:ENSG00000248092 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1245818752 Functional Loss SNV dbSNP153 33..33 33 - - - 11421 RMVar_ID_11421 Human_SNP_ID_229802023 A-to-I Human chr5 - 43595338 43595338 43595338 CGCCTGCCTCGGCCTCCCAAACTGCTGGGACTACAGGCATGAGCCACTGCACCTGGCCCACTATA CGCCTGCCTCGGCCTCCCAAACTGCTGGGACTGCAGGCATGAGCCACTGCACCTGGCCCACTATA T C NNT-AS1 Ensembl:ENSG00000248092 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025548690 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8269038 11422 RMVar_ID_11422 Human_SNP_ID_230139018 A-to-I Human chr5 - 44800589 44800589 44800589 AGGCACAAACCATCATGCCTGGCTAATTATTTATTTTTTGCATGGGTAGATCTCATTACATCGCT AGGCACAAACCATCATGCCTGGCTAATTATTTGTTTTTTGCATGGGTAGATCTCATTACATCGCT T C MRPS30-DT Ensembl:ENSG00000251141 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1046412075 Functional Loss SNV dbSNP153 33..33 33 - - - 11423 RMVar_ID_11423 Human_SNP_ID_230142405 A-to-I Human chr5 + 44813170 44813170 44813170 CACACCCAGTTTCATCTGTTACCTGACAAATTAAGAAGGGAAAGGCTTTTGAGACAAAACTGTGC CACACCCAGTTTCATCTGTTACCTGACAAATTGAGAAGGGAAAGGCTTTTGAGACAAAACTGTGC A G MRPS30 Ensembl:ENSG00000112996 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1373620981 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1654983,Human_RBP_ID_1995836,Human_RBP_ID_4832686,Human_RBP_ID_8616702,Human_RBP_ID_15455111,Human_RBP_ID_17301968,Human_RBP_ID_18358921,Human_RBP_ID_22460040,Human_RBP_ID_24107365 Human_Splice_Rec_649054,Human_Splice_Rec_649062,Human_Splice_Rec_649066 RMVar_hsa_circ_231311,RMVar_hsa_circ_372380,RMVar_hsa_circ_59004 11424 RMVar_ID_11424 Human_SNP_ID_230142837 A-to-I Human chr5 + 44814997 44814997 44814997 CACAGATGGAAAATACTTTTCCTTTTTCTGCTACCAGCTAAATACTTTGGCACTGACTACACAAG CACAGATGGAAAATACTTTTCCTTTTTCTGCTGCCAGCTAAATACTTTGGCACTGACTACACAAG A G MRPS30 Ensembl:ENSG00000112996 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1437186757 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_77520,Human_RBP_ID_8616704,Human_RBP_ID_22301234,Human_RBP_ID_22404358,Human_RBP_ID_27082152,Human_RBP_ID_27516140 Human_Splice_Rec_649056,Human_Splice_Rec_649064 11425 RMVar_ID_11425 Human_SNP_ID_230143006 A-to-I Human chr5 + 44815550 44815550 44815550 AGTAATTAAAAGAACCCACTGCAGCTGGGTGCAATGGCTCATGCCTGTAATCGCAACACTTTGGG AGTAATTAAAAGAACCCACTGCAGCTGGGTGCCATGGCTCATGCCTGTAATCGCAACACTTTGGG A C MRPS30 Ensembl:ENSG00000112996 Protein coding exon GSE100210;GSE107867 HepG2 cell line;ASD brains,temporal_cortex - 29129909,30559470 RNA-Seq:(High) rs898209819 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_649067 11426 RMVar_ID_11426 Human_SNP_ID_230143027 A-to-I Human chr5 + 44815626 44815626 44815626 GGTGGATCGCTTGAGTCCAGCAGTTTGAGACCAGCCTGGGCAACATGGCAAAACCCCATCTCTAG GGTGGATCGCTTGAGTCCAGCAGTTTGAGACCCGCCTGGGCAACATGGCAAAACCCCATCTCTAG A C MRPS30 Ensembl:ENSG00000112996 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1372775532 Functional Loss SNV dbSNP153 33..33 33 - - - 11427 RMVar_ID_11427 Human_SNP_ID_230143032 A-to-I Human chr5 + 44815668 44815668 44815668 ACATGGCAAAACCCCATCTCTAGTAAAAATACAAAAATTAGCCTGTCCTGGTGGTGCATGCCTGT ACATGGCAAAACCCCATCTCTAGTAAAAATACGAAAATTAGCCTGTCCTGGTGGTGCATGCCTGT A G MRPS30 Ensembl:ENSG00000112996 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1021471879 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15455155,Human_RBP_ID_25898580,Human_RBP_ID_26527335 11428 RMVar_ID_11428 Human_SNP_ID_230143046 A-to-I Human chr5 + 44815737 44815737 44815737 CCAGCTAGTCTGGAGGCTGAGGCACAAGAATCACTGGAACCCGGGAGGCAGAGTTTGCAGTGAAC CCAGCTAGTCTGGAGGCTGAGGCACAAGAATCGCTGGAACCCGGGAGGCAGAGTTTGCAGTGAAC A G MRPS30 Ensembl:ENSG00000112996 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1303389341 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7442613,Human_RBP_ID_15455156,Human_RBP_ID_27516151 11429 RMVar_ID_11429 Human_SNP_ID_230144009 A-to-I Human chr5 + 44819764 44819764 44819764 ACTGAGTCTGGCTCTGTTGCCTAGGCTCAAGTACTGTGGATCTTGGCTCACTGCAGCCTCCACCT ACTGAGTCTGGCTCTGTTGCCTAGGCTCAAGTGCTGTGGATCTTGGCTCACTGCAGCCTCCACCT A G MRPS30 Ensembl:ENSG00000112996 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1408557917 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_642931,Human_RBP_ID_4855541,Human_RBP_ID_7442757,Human_RBP_ID_8890370,Human_RBP_ID_15455369,Human_RBP_ID_17413851 11430 RMVar_ID_11430 Human_SNP_ID_230144015 A-to-I Human chr5 + 44819810 44819810 44819810 CTCACTGCAGCCTCCACCTCTTGGATTCAAGCAGTTCTCCTGCCTCAGCCTCCCGAGTAGCTGGG CTCACTGCAGCCTCCACCTCTTGGATTCAAGCCGTTCTCCTGCCTCAGCCTCCCGAGTAGCTGGG A C MRPS30 Ensembl:ENSG00000112996 Protein coding exon GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1199769849 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15455378 11431 RMVar_ID_11431 Human_SNP_ID_230160314 A-to-I Human chr5 + 44886418 44886418 44886418 TTGTAGTCATCTTTGGCTCTCTAGTTACTCCTATGGAAAGACCTCAATCAAAGTTTGAGGATATT TTGTAGTCATCTTTGGCTCTCTAGTTACTCCTGTGGAAAGACCTCAATCAAAGTTTGAGGATATT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs961280245 Functional Loss SNV dbSNP153 33..33 33 - - - 11432 RMVar_ID_11432 Human_SNP_ID_614249112 A-to-I Human chr16 + 90025813 90025813 90025813 TGGAGGCTGAGGCAGGAGAATTGTTTGAACCCAAGAGGTGGAGGTTGCAGTGAGCCAAGGCAGCC TGGAGGCTGAGGCAGGAGAATTGTTTGAACCCTAGAGGTGGAGGTTGCAGTGAGCCAAGGCAGCC A T GAS8 Ensembl:ENSG00000141013 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1567844474 Functional Loss SNV dbSNP153 33..33 33 - - - 11433 RMVar_ID_11433 Human_SNP_ID_614251001 A-to-I Human chr16 + 90030818 90030818 90030818 AAAAAAAGTTTTTGCAGAGATGGGGTCTTGCTATGTTGCCCAAGCTGGTCTTCAGCTCCTGGGCG AAAAAAAGTTTTTGCAGAGATGGGGTCTTGCTCTGTTGCCCAAGCTGGTCTTCAGCTCCTGGGCG A C GAS8 Ensembl:ENSG00000141013 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1439473539 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_365495 11434 RMVar_ID_11434 Human_SNP_ID_614251002 A-to-I Human chr16 + 90030818 90030818 90030818 AAAAAAAGTTTTTGCAGAGATGGGGTCTTGCTATGTTGCCCAAGCTGGTCTTCAGCTCCTGGGCG AAAAAAAGTTTTTGCAGAGATGGGGTCTTGCTGTGTTGCCCAAGCTGGTCTTCAGCTCCTGGGCG A G GAS8 Ensembl:ENSG00000141013 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1439473539 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_365495 11435 RMVar_ID_11435 Human_SNP_ID_614279062 A-to-I Human chr16 + 90149520 90149520 90149520 CAACAGTTAGCTAGGCGTTGTGGCACATCCCTATAATTCCAGCTACTCGGGAGGCTGAGGCAGGA CAACAGTTAGCTAGGCGTTGTGGCACATCCCTGTAATTCCAGCTACTCGGGAGGCTGAGGCAGGA A G FAM157C Ensembl:ENSG00000260528 lincRNA intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1390323990 Functional Loss SNV dbSNP153 33..33 33 - - - 11436 RMVar_ID_11436 Human_SNP_ID_614282392 A-to-I Human chr16 - 90167847 90167847 90167847 GAGAGGCCGACTTGAGGAGGTTCTGGGCCCGGAGAGGCCGCCGGAAGGGAAAAACTGGGCCTGGA GAGAGGCCGACTTGAGGAGGTTCTGGGCCCGGGGAGGCCGCCGGAAGGGAAAAACTGGGCCTGGA T C AC133919.2 Ensembl:ENSG00000261172 lincRNA intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1555519268 Functional Loss SNV dbSNP153 33..33 33 - - - 11437 RMVar_ID_11437 Human_SNP_ID_19073647 A-to-I Human chr1 + 75730565 75730565 75730565 GTCATTTTTCCTTTTTTTTTTTTTTAAGAGACAGGGTTTCACTCTGTCACCCAAGCTGGATGCAA GTCATTTTTCCTTTTTTTTTTTTTTAAGAGACGGGGTTTCACTCTGTCACCCAAGCTGGATGCAA A G ACADM Ensembl:ENSG00000117054 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs527489931 Functional Loss SNV dbSNP153 33..33 33 - - - 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 11438 RMVar_ID_11438 Human_SNP_ID_19073710 A-to-I Human chr1 + 75730795 75730795 75730795 ATGGTTCACCTGCCTCAGCCTCCCAAAATTCTAGAATTATAGGCATGAGCTACCGTGCCCAGACT ATGGTTCACCTGCCTCAGCCTCCCAAAATTCTGGAATTATAGGCATGAGCTACCGTGCCCAGACT A G ACADM Ensembl:ENSG00000117054 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs986962627 Functional Loss SNV dbSNP153 33..33 33 - - - 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 11439 RMVar_ID_11439 Human_SNP_ID_19074114 A-to-I Human chr1 + 75732071 75732071 75732071 CTAGTTGAGAAGCTGTGGTGGGAAGATCATTTAAGGCCAGGAGGTCGAGGCTACAGTGAGTCGTA CTAGTTGAGAAGCTGTGGTGGGAAGATCATTTGAGGCCAGGAGGTCGAGGCTACAGTGAGTCGTA A G ACADM Ensembl:ENSG00000117054 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1359058054 Functional Loss SNV dbSNP153 33..33 33 - - - 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 11440 RMVar_ID_11440 Human_SNP_ID_19077350 A-to-I Human chr1 + 75743863 75743863 75743863 CAATATAATCCCTATATACCACCTCTTTGGTTATATCATCAATCACTGCGTTTACAACAGGCTGT CAATATAATCCCTATATACCACCTCTTTGGTTGTATCATCAATCACTGCGTTTACAACAGGCTGT A G ACADM Ensembl:ENSG00000117054 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878957247 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50514,RMVar_hsa_circ_282895,RMVar_hsa_circ_66379,RMVar_hsa_circ_278267,RMVar_hsa_circ_133985,RMVar_hsa_circ_133986,RMVar_hsa_circ_296785,RMVar_hsa_circ_344983,RMVar_hsa_circ_133988,RMVar_hsa_circ_357254,RMVar_hsa_circ_133987,RMVar_hsa_circ_288990,RMVar_hsa_circ_274456,RMVar_hsa_circ_355439,RMVar_hsa_circ_366597,RMVar_hsa_circ_336870,RMVar_hsa_circ_133994,RMVar_hsa_circ_274656,RMVar_hsa_circ_314373,RMVar_hsa_circ_133996,RMVar_hsa_circ_11880,RMVar_hsa_circ_133995 11441 RMVar_ID_11441 Human_SNP_ID_19077351 A-to-I Human chr1 + 75743865 75743865 75743865 ATATAATCCCTATATACCACCTCTTTGGTTATATCATCAATCACTGCGTTTACAACAGGCTGTTC ATATAATCCCTATATACCACCTCTTTGGTTATGTCATCAATCACTGCGTTTACAACAGGCTGTTC A G ACADM Ensembl:ENSG00000117054 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878882768 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50514,RMVar_hsa_circ_282895,RMVar_hsa_circ_66379,RMVar_hsa_circ_278267,RMVar_hsa_circ_133985,RMVar_hsa_circ_133986,RMVar_hsa_circ_296785,RMVar_hsa_circ_344983,RMVar_hsa_circ_133988,RMVar_hsa_circ_357254,RMVar_hsa_circ_133987,RMVar_hsa_circ_288990,RMVar_hsa_circ_274456,RMVar_hsa_circ_355439,RMVar_hsa_circ_366597,RMVar_hsa_circ_336870,RMVar_hsa_circ_133994,RMVar_hsa_circ_274656,RMVar_hsa_circ_314373,RMVar_hsa_circ_133996,RMVar_hsa_circ_11880,RMVar_hsa_circ_133995 11442 RMVar_ID_11442 Human_SNP_ID_19077352 A-to-I Human chr1 + 75743865 75743865 75743865 ATATAATCCCTATATACCACCTCTTTGGTTATATCATCAATCACTGCGTTTACAACAGGCTGTTC ATATAATCCCTATATACCACCTCTTTGGTTATTTCATCAATCACTGCGTTTACAACAGGCTGTTC A T ACADM Ensembl:ENSG00000117054 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878882768 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50514,RMVar_hsa_circ_282895,RMVar_hsa_circ_66379,RMVar_hsa_circ_278267,RMVar_hsa_circ_133985,RMVar_hsa_circ_133986,RMVar_hsa_circ_296785,RMVar_hsa_circ_344983,RMVar_hsa_circ_133988,RMVar_hsa_circ_357254,RMVar_hsa_circ_133987,RMVar_hsa_circ_288990,RMVar_hsa_circ_274456,RMVar_hsa_circ_355439,RMVar_hsa_circ_366597,RMVar_hsa_circ_336870,RMVar_hsa_circ_133994,RMVar_hsa_circ_274656,RMVar_hsa_circ_314373,RMVar_hsa_circ_133996,RMVar_hsa_circ_11880,RMVar_hsa_circ_133995 11443 RMVar_ID_11443 Human_SNP_ID_19077353 A-to-I Human chr1 + 75743868 75743868 75743868 TAATCCCTATATACCACCTCTTTGGTTATATCATCAATCACTGCGTTTACAACAGGCTGTTCCTG TAATCCCTATATACCACCTCTTTGGTTATATCGTCAATCACTGCGTTTACAACAGGCTGTTCCTG A G ACADM Ensembl:ENSG00000117054 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879207773 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50514,RMVar_hsa_circ_282895,RMVar_hsa_circ_66379,RMVar_hsa_circ_278267,RMVar_hsa_circ_133985,RMVar_hsa_circ_133986,RMVar_hsa_circ_296785,RMVar_hsa_circ_344983,RMVar_hsa_circ_133988,RMVar_hsa_circ_357254,RMVar_hsa_circ_133987,RMVar_hsa_circ_288990,RMVar_hsa_circ_274456,RMVar_hsa_circ_355439,RMVar_hsa_circ_366597,RMVar_hsa_circ_336870,RMVar_hsa_circ_133994,RMVar_hsa_circ_274656,RMVar_hsa_circ_314373,RMVar_hsa_circ_133996,RMVar_hsa_circ_11880,RMVar_hsa_circ_133995 11444 RMVar_ID_11444 Human_SNP_ID_19077385 A-to-I Human chr1 - 75743996 75743996 75743996 TTTTTAATGAGATTGATGTGAGTAACATCCAGAAGATGAGGGCTCGGCACAAAGAGGCTTTTTTG TTTTTAATGAGATTGATGTGAGTAACATCCAGGAGATGAGGGCTCGGCACAAAGAGGCTTTTTTG T C DLSTP1 Ensembl:ENSG00000181227 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs954651277 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1898130 11445 RMVar_ID_11445 Human_SNP_ID_19077542 A-to-I Human chr1 - 75744587 75744587 75744587 GTGTCTTCAGTGTTCGCTTCTTCAGAACTACAACTGTATGCAAGTATGACTTGGTTACAGTCAAA GTGTCTTCAGTGTTCGCTTCTTCAGAACTACAGCTGTATGCAAGTATGACTTGGTTACAGTCAAA T C DLSTP1 Ensembl:ENSG00000181227 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs17097423 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8241219 11446 RMVar_ID_11446 Human_SNP_ID_19079348 A-to-I Human chr1 + 75751767 75751767 75751767 GTGATCTGCCTGCCTCGGCCTCCCAAAGTGCTAGGATTACAGGCCTGAACCACTGCGCCTGGCCT GTGATCTGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCCTGAACCACTGCGCCTGGCCT A G ACADM Ensembl:ENSG00000117054 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs973558860 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_288990,RMVar_hsa_circ_54465,RMVar_hsa_circ_11880 11447 RMVar_ID_11447 Human_SNP_ID_19090099 A-to-I Human chr1 + 75791459 75791459 75791459 GGAATTTAACAGGCATCTTTTTTTTTGTTTGTAGGGGAAGCTTGATGCTATTAATGTGGAAAAGG GGAATTTAACAGGCATCTTTTTTTTTGTTTGTTGGGGAAGCTTGATGCTATTAATGTGGAAAAGG A T RABGGTB Ensembl:ENSG00000137955 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1336560764 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_859413,Human_RBP_ID_1155965,Human_RBP_ID_2165093,Human_RBP_ID_3933655,Human_RBP_ID_5338063,Human_RBP_ID_5519875,Human_RBP_ID_5863441,Human_RBP_ID_9270207,Human_RBP_ID_9342832,Human_RBP_ID_18965693,Human_RBP_ID_19041532,Human_RBP_ID_22563548,Human_RBP_ID_22638766,Human_RBP_ID_22871329,Human_RBP_ID_23412600,Human_RBP_ID_24726019 RMVar_hsa_circ_25342,RMVar_hsa_circ_73706,RMVar_hsa_circ_282257,RMVar_hsa_circ_305194,RMVar_hsa_circ_134001,RMVar_hsa_circ_65468,RMVar_hsa_circ_76212,RMVar_hsa_circ_376004,RMVar_hsa_circ_134005,RMVar_hsa_circ_134006 11448 RMVar_ID_11448 Human_SNP_ID_19388012 A-to-I Human chr1 + 77044032 77044032 77044032 TGCTCTTGTCCATTGTTCCCTGTCACCCATTTAGAAGAGAACGCAAGGGTCCATAAAGTAATAGC TGCTCTTGTCCATTGTTCCCTGTCACCCATTTGGAAGAGAACGCAAGGGTCCATAAAGTAATAGC A G ST6GALNAC5 Ensembl:ENSG00000117069 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs780403105 Functional Loss SNV dbSNP153 33..33 33 - - - 11449 RMVar_ID_11449 Human_SNP_ID_19399009 A-to-I Human chr1 - 77092049 77092049 77092049 TCATTTGGAAAAGAAACAATTGTGAAGACATTAAATTCTCACTAACAGAAGTAACTTTGGTTAAT TCATTTGGAAAAGAAACAATTGTGAAGACATTGAATTCTCACTAACAGAAGTAACTTTGGTTAAT T C PIGK Ensembl:ENSG00000142892 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1008288438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_362374,Human_RBP_ID_1753934,Human_RBP_ID_5864115,Human_RBP_ID_8050054,Human_RBP_ID_17337145,Human_RBP_ID_17757917,Human_RBP_ID_23413082,Human_RBP_ID_26383144 Human_miRNA_ID_2917662 RMVar_hsa_circ_98474,RMVar_hsa_circ_134034 11450 RMVar_ID_11450 Human_SNP_ID_19427617 A-to-I Human chr1 - 77218846 77218845 77218846 AGTGTTTATTAAAACTCTCAAGTTTCTGGCTTAGGGGCAACACGTCTGGGTTAAGAAATGGAAGA AGTGTTTATTAAAACTCTCAAGTTTCTGGCTT_GGGGCAACACGTCTGGGTTAAGAAATGGAAGA CT C PIGK Ensembl:ENSG00000142892 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1434865316 Functional Loss DEL dbSNP153 33..33 33 - - - 11451 RMVar_ID_11451 Human_SNP_ID_19456777 A-to-I Human chr1 + 77346687 77346687 77346687 CCCACCTAATTTTTCGTATGTTTTGTAGAGACAGGGTCTCACTTTGTCCCTCAGGCTGGTCTCGG CCCACCTAATTTTTCGTATGTTTTGTAGAGACGGGGTCTCACTTTGTCCCTCAGGCTGGTCTCGG A G AK5 Ensembl:ENSG00000154027 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1286247784 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5169 11452 RMVar_ID_11452 Human_SNP_ID_19514699 A-to-I Human chr1 - 77588988 77588986 77588988 CCTGTCCCAGCTACGTGGGAGGCTGAAGTGAGAGGATTGCTTGAGCTCGAGAGGTAGAGGCTGCA CCTGTCCCAGCTACGTGGGAGGCTGAAGTGAG__GATTGCTTGAGCTCGAGAGGTAGAGGCTGCA CCT C AC118549.1 Ensembl:ENSG00000036549 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1411033360 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_11106056 RMVar_hsa_circ_63492,RMVar_hsa_circ_106072,RMVar_hsa_circ_134051,RMVar_hsa_circ_134053,RMVar_hsa_circ_51651,RMVar_hsa_circ_349770,RMVar_hsa_circ_37660,RMVar_hsa_circ_338769,RMVar_hsa_circ_134054,RMVar_hsa_circ_20486,RMVar_hsa_circ_134060,RMVar_hsa_circ_25738,RMVar_hsa_circ_134057,RMVar_hsa_circ_134058,RMVar_hsa_circ_285562,RMVar_hsa_circ_332186,RMVar_hsa_circ_134061,RMVar_hsa_circ_81995,RMVar_hsa_circ_134062 11453 RMVar_ID_11453 Human_SNP_ID_19514700 A-to-I Human chr1 - 77588988 77588988 77588988 CCTGTCCCAGCTACGTGGGAGGCTGAAGTGAGAGGATTGCTTGAGCTCGAGAGGTAGAGGCTGCA CCTGTCCCAGCTACGTGGGAGGCTGAAGTGAGGGGATTGCTTGAGCTCGAGAGGTAGAGGCTGCA T C AC118549.1 Ensembl:ENSG00000036549 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs940795435 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11106056 RMVar_hsa_circ_63492,RMVar_hsa_circ_106072,RMVar_hsa_circ_134051,RMVar_hsa_circ_134053,RMVar_hsa_circ_51651,RMVar_hsa_circ_349770,RMVar_hsa_circ_37660,RMVar_hsa_circ_338769,RMVar_hsa_circ_134054,RMVar_hsa_circ_20486,RMVar_hsa_circ_134060,RMVar_hsa_circ_25738,RMVar_hsa_circ_134057,RMVar_hsa_circ_134058,RMVar_hsa_circ_285562,RMVar_hsa_circ_332186,RMVar_hsa_circ_134061,RMVar_hsa_circ_81995,RMVar_hsa_circ_134062 11454 RMVar_ID_11454 Human_SNP_ID_19517979 A-to-I Human chr1 - 77603960 77603960 77603960 GGGTTCTCACTATGTTGCCTGGGCTAGTCTCAAAATCCAAGCATCAAGTAATCCTCCTGCATCAG GGGTTCTCACTATGTTGCCTGGGCTAGTCTCAGAATCCAAGCATCAAGTAATCCTCCTGCATCAG T C AC118549.1 Ensembl:ENSG00000036549 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs972118791 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557230 RMVar_hsa_circ_63492,RMVar_hsa_circ_106072,RMVar_hsa_circ_134051,RMVar_hsa_circ_134053,RMVar_hsa_circ_51651,RMVar_hsa_circ_349770,RMVar_hsa_circ_37660,RMVar_hsa_circ_338769,RMVar_hsa_circ_134054,RMVar_hsa_circ_20486,RMVar_hsa_circ_134060,RMVar_hsa_circ_25738,RMVar_hsa_circ_134057,RMVar_hsa_circ_134058,RMVar_hsa_circ_285562,RMVar_hsa_circ_332186,RMVar_hsa_circ_134061,RMVar_hsa_circ_81995,RMVar_hsa_circ_134062,RMVar_hsa_circ_134063 11455 RMVar_ID_11455 Human_SNP_ID_19518008 A-to-I Human chr1 - 77604052 77604052 77604052 GCGATCCTCCCACTTCAGCCTCCTGAGTAGCTAGGACTACCGGTGTGGACCACCATACCCAGTAA GCGATCCTCCCACTTCAGCCTCCTGAGTAGCTGGGACTACCGGTGTGGACCACCATACCCAGTAA T C AC118549.1 Ensembl:ENSG00000036549 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs891180529 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63492,RMVar_hsa_circ_106072,RMVar_hsa_circ_134051,RMVar_hsa_circ_134053,RMVar_hsa_circ_51651,RMVar_hsa_circ_349770,RMVar_hsa_circ_37660,RMVar_hsa_circ_338769,RMVar_hsa_circ_134054,RMVar_hsa_circ_20486,RMVar_hsa_circ_134060,RMVar_hsa_circ_25738,RMVar_hsa_circ_134057,RMVar_hsa_circ_134058,RMVar_hsa_circ_285562,RMVar_hsa_circ_332186,RMVar_hsa_circ_134061,RMVar_hsa_circ_81995,RMVar_hsa_circ_134062,RMVar_hsa_circ_134063 11456 RMVar_ID_11456 Human_SNP_ID_19530909 A-to-I Human chr1 - 77659925 77659925 77659925 GGGAGGCTAAAGCAGGAGTATCGCTTGAGCCCAGGAATTTGAGGTGGCAGTGAGCTATTGTCCTG GGGAGGCTAAAGCAGGAGTATCGCTTGAGCCCGGGAATTTGAGGTGGCAGTGAGCTATTGTCCTG T C AC118549.1 Ensembl:ENSG00000036549 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1446929019 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_134070 11457 RMVar_ID_11457 Human_SNP_ID_19531345 A-to-I Human chr1 - 77661908 77661908 77661908 GGAGATTTAGGTGGGAGGATTGCTTGAGCCCAAGAGTTCAAGGTTGCAGTGAGCTATGATCGTGT GGAGATTTAGGTGGGAGGATTGCTTGAGCCCAGGAGTTCAAGGTTGCAGTGAGCTATGATCGTGT T C AC118549.1 Ensembl:ENSG00000036549 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1375531603 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_134070 11458 RMVar_ID_11458 Human_SNP_ID_19534733 A-to-I Human chr1 - 77676242 77676242 77676242 GGATCACTTGACCCCAAAAGATTGAGGCTACAATGAGCCCAGATTGCGCCCCTACACTCCAGCCT GGATCACTTGACCCCAAAAGATTGAGGCTACAGTGAGCCCAGATTGCGCCCCTACACTCCAGCCT T C AC118549.1 Ensembl:ENSG00000036549 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1325318900 Functional Loss SNV dbSNP153 33..33 33 - - - 11459 RMVar_ID_11459 Human_SNP_ID_19534929 A-to-I Human chr1 - 77677156 77677156 77677156 TTTTTGTATTTTTGTAGAGATGGGGTTTCACCATGTTAGTCAGGCTGGTCTGGAACTCCTGACCT TTTTTGTATTTTTGTAGAGATGGGGTTTCACCGTGTTAGTCAGGCTGGTCTGGAACTCCTGACCT T C AC118549.1 Ensembl:ENSG00000036549 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1038245655 Functional Loss SNV dbSNP153 33..33 33 - - - 11460 RMVar_ID_11460 Human_SNP_ID_19534930 A-to-I Human chr1 - 77677156 77677156 77677156 TTTTTGTATTTTTGTAGAGATGGGGTTTCACCATGTTAGTCAGGCTGGTCTGGAACTCCTGACCT TTTTTGTATTTTTGTAGAGATGGGGTTTCACCCTGTTAGTCAGGCTGGTCTGGAACTCCTGACCT T G AC118549.1 Ensembl:ENSG00000036549 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1038245655 Functional Loss SNV dbSNP153 33..33 33 - - - 11461 RMVar_ID_11461 Human_SNP_ID_19534937 A-to-I Human chr1 - 77677173 77677173 77677173 CCACCACGCCCGGCTAATTTTTGTATTTTTGTAGAGATGGGGTTTCACCATGTTAGTCAGGCTGG CCACCACGCCCGGCTAATTTTTGTATTTTTGTGGAGATGGGGTTTCACCATGTTAGTCAGGCTGG T C AC118549.1 Ensembl:ENSG00000036549 Protein coding intron GSE123020:GSM3490829,GSM3490830,GSM3490831 esophageal squamous carcinoma cells,EC109 cell line - 32596459 RNA-Seq:(High) rs1324765958 Functional Loss SNV dbSNP153 33..33 33 - - - 11462 RMVar_ID_11462 Human_SNP_ID_19534948 A-to-I Human chr1 - 77677214 77677214 77677214 CCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGATGCACACCACCACGCCCGGCTAATTTTTGT CCTGCCTCAGCCTCCTGAGTAGCTGGGACTACGGATGCACACCACCACGCCCGGCTAATTTTTGT T C AC118549.1 Ensembl:ENSG00000036549 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs889087774 Functional Loss SNV dbSNP153 33..33 33 - - - 11463 RMVar_ID_11463 Human_SNP_ID_19534953 A-to-I Human chr1 - 77677251 77677251 77677251 TCACTGCAGCCTCTACCCCCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGA TCACTGCAGCCTCTACCCCCCGGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGA T C AC118549.1 Ensembl:ENSG00000036549 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs967443972 Functional Loss SNV dbSNP153 33..33 33 - - - 11464 RMVar_ID_11464 Human_SNP_ID_19540175 A-to-I Human chr1 - 77698346 77698346 77698346 ACCATAGGCCAGGTGTAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGTAG ACCATAGGCCAGGTGTAGTGGCTCACGCCTGTCATCCCAGCACTTTGGGAGGCTGAGGTGGGTAG T G USP33 Ensembl:ENSG00000077254 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs948210218 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41163,RMVar_hsa_circ_115321,RMVar_hsa_circ_134072,RMVar_hsa_circ_333613,RMVar_hsa_circ_361333,RMVar_hsa_circ_134074,RMVar_hsa_circ_9107 11465 RMVar_ID_11465 Human_SNP_ID_19540486 A-to-I Human chr1 - 77699454 77699454 77699454 GGAGTGGAGTGGCGTGATCTCAGCTCATTGCAACCTCCTCCTGGGTTCAGACGATTGTCCTGCCT GGAGTGGAGTGGCGTGATCTCAGCTCATTGCAGCCTCCTCCTGGGTTCAGACGATTGTCCTGCCT T C USP33 Ensembl:ENSG00000077254 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1298852366 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41163,RMVar_hsa_circ_115321,RMVar_hsa_circ_134072,RMVar_hsa_circ_333613,RMVar_hsa_circ_361333,RMVar_hsa_circ_134074,RMVar_hsa_circ_9107 11466 RMVar_ID_11466 Human_SNP_ID_19542060 A-to-I Human chr1 - 77705536 77705536 77705536 TGAGCTATGACCATGACCCTGCACTCCAGCCTAGGCAACAGAGCAAGACCCTGTCTTTAAAAATA TGAGCTATGACCATGACCCTGCACTCCAGCCTGGGCAACAGAGCAAGACCCTGTCTTTAAAAATA T C USP33 Ensembl:ENSG00000077254 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1373994813 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11110378 RMVar_hsa_circ_41163,RMVar_hsa_circ_115321,RMVar_hsa_circ_134072,RMVar_hsa_circ_333613,RMVar_hsa_circ_18664,RMVar_hsa_circ_299131,RMVar_hsa_circ_134074,RMVar_hsa_circ_9107,RMVar_hsa_circ_299345,RMVar_hsa_circ_305980,RMVar_hsa_circ_39034,RMVar_hsa_circ_290819,RMVar_hsa_circ_36160,RMVar_hsa_circ_134075,RMVar_hsa_circ_134077,RMVar_hsa_circ_134078,RMVar_hsa_circ_134076 11467 RMVar_ID_11467 Human_SNP_ID_19542965 A-to-I Human chr1 - 77709439 77709439 77709439 CTGGTCATAGTTCACTGTAACCTTGAACTCCTAGGCTAAAGGGATCCTCCTGCCTCAGCATCCCG CTGGTCATAGTTCACTGTAACCTTGAACTCCTTGGCTAAAGGGATCCTCCTGCCTCAGCATCCCG T A USP33 Ensembl:ENSG00000077254 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1182389390 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41163,RMVar_hsa_circ_115321,RMVar_hsa_circ_134072,RMVar_hsa_circ_333613,RMVar_hsa_circ_18664,RMVar_hsa_circ_299131,RMVar_hsa_circ_134074,RMVar_hsa_circ_9107,RMVar_hsa_circ_299345,RMVar_hsa_circ_305980,RMVar_hsa_circ_39034,RMVar_hsa_circ_290819,RMVar_hsa_circ_36160,RMVar_hsa_circ_134075,RMVar_hsa_circ_134077,RMVar_hsa_circ_134078,RMVar_hsa_circ_134076 11468 RMVar_ID_11468 Human_SNP_ID_19547201 A-to-I Human chr1 - 77726087 77726087 77726087 AAATGAGGTGGGCCTGGTGGCACATGCCTGTAATCTCAGCTACTTGGGAGGCTGAGGCAGAAGAA AAATGAGGTGGGCCTGGTGGCACATGCCTGTAGTCTCAGCTACTTGGGAGGCTGAGGCAGAAGAA T C USP33 Ensembl:ENSG00000077254 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1428222226 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2191,RMVar_hsa_circ_18664,RMVar_hsa_circ_39034,RMVar_hsa_circ_36160,RMVar_hsa_circ_329724,RMVar_hsa_circ_346129,RMVar_hsa_circ_348957,RMVar_hsa_circ_297810,RMVar_hsa_circ_305394,RMVar_hsa_circ_134080,RMVar_hsa_circ_134081,RMVar_hsa_circ_340348,RMVar_hsa_circ_134094,RMVar_hsa_circ_20124,RMVar_hsa_circ_134090,RMVar_hsa_circ_318880,RMVar_hsa_circ_342460,RMVar_hsa_circ_315029,RMVar_hsa_circ_298078,RMVar_hsa_circ_298802,RMVar_hsa_circ_82672,RMVar_hsa_circ_88317,RMVar_hsa_circ_69781,RMVar_hsa_circ_134095,RMVar_hsa_circ_33637,RMVar_hsa_circ_4122,RMVar_hsa_circ_134100,RMVar_hsa_circ_134092,RMVar_hsa_circ_134093,RMVar_hsa_circ_89784,RMVar_hsa_circ_340465,RMVar_hsa_circ_361504,RMVar_hsa_circ_267073,RMVar_hsa_circ_317121,RMVar_hsa_circ_134101,RMVar_hsa_circ_134102,RMVar_hsa_circ_322401,RMVar_hsa_circ_334373,RMVar_hsa_circ_285201,RMVar_hsa_circ_311285,RMVar_hsa_circ_281112,RMVar_hsa_circ_134104,RMVar_hsa_circ_134106,RMVar_hsa_circ_134107,RMVar_hsa_circ_134105,RMVar_hsa_circ_134103 11469 RMVar_ID_11469 Human_SNP_ID_19547204 A-to-I Human chr1 - 77726118 77726118 77726118 TGGTGAAACCCCATCTCTACTAAAAATACAAAAATGAGGTGGGCCTGGTGGCACATGCCTGTAAT TGGTGAAACCCCATCTCTACTAAAAATACAAAGATGAGGTGGGCCTGGTGGCACATGCCTGTAAT T C USP33 Ensembl:ENSG00000077254 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs890024716 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2191,RMVar_hsa_circ_18664,RMVar_hsa_circ_39034,RMVar_hsa_circ_36160,RMVar_hsa_circ_329724,RMVar_hsa_circ_346129,RMVar_hsa_circ_348957,RMVar_hsa_circ_297810,RMVar_hsa_circ_305394,RMVar_hsa_circ_134080,RMVar_hsa_circ_134081,RMVar_hsa_circ_340348,RMVar_hsa_circ_134094,RMVar_hsa_circ_20124,RMVar_hsa_circ_134090,RMVar_hsa_circ_318880,RMVar_hsa_circ_342460,RMVar_hsa_circ_315029,RMVar_hsa_circ_298078,RMVar_hsa_circ_298802,RMVar_hsa_circ_82672,RMVar_hsa_circ_88317,RMVar_hsa_circ_69781,RMVar_hsa_circ_134095,RMVar_hsa_circ_33637,RMVar_hsa_circ_4122,RMVar_hsa_circ_134100,RMVar_hsa_circ_134092,RMVar_hsa_circ_134093,RMVar_hsa_circ_89784,RMVar_hsa_circ_340465,RMVar_hsa_circ_361504,RMVar_hsa_circ_267073,RMVar_hsa_circ_317121,RMVar_hsa_circ_134101,RMVar_hsa_circ_134102,RMVar_hsa_circ_322401,RMVar_hsa_circ_334373,RMVar_hsa_circ_285201,RMVar_hsa_circ_311285,RMVar_hsa_circ_281112,RMVar_hsa_circ_134104,RMVar_hsa_circ_134106,RMVar_hsa_circ_134107,RMVar_hsa_circ_134105,RMVar_hsa_circ_134103 11470 RMVar_ID_11470 Human_SNP_ID_19548904 A-to-I Human chr1 - 77732841 77732840 77732842 TGCAATGAGCCTAGGTCATGCCATTGCACTCTAGCCCAGGTGACAGTGTGAGACTCCGTCAAAAA TGCAATGAGCCTAGGTCATGCCATTGCACTC__GCCCAGGTGACAGTGTGAGACTCCGTCAAAAA CTA C USP33 Ensembl:ENSG00000077254 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1557851065 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_2191,RMVar_hsa_circ_18664,RMVar_hsa_circ_348957,RMVar_hsa_circ_297810,RMVar_hsa_circ_305394,RMVar_hsa_circ_134080,RMVar_hsa_circ_134081,RMVar_hsa_circ_340348,RMVar_hsa_circ_134090,RMVar_hsa_circ_342460,RMVar_hsa_circ_315029,RMVar_hsa_circ_298802,RMVar_hsa_circ_88317,RMVar_hsa_circ_69781,RMVar_hsa_circ_33637,RMVar_hsa_circ_4122,RMVar_hsa_circ_134100,RMVar_hsa_circ_134092,RMVar_hsa_circ_134093,RMVar_hsa_circ_89784,RMVar_hsa_circ_361504,RMVar_hsa_circ_267073,RMVar_hsa_circ_134102,RMVar_hsa_circ_334373,RMVar_hsa_circ_285201,RMVar_hsa_circ_311285,RMVar_hsa_circ_281112,RMVar_hsa_circ_134104,RMVar_hsa_circ_134106,RMVar_hsa_circ_134107,RMVar_hsa_circ_134105,RMVar_hsa_circ_285233,RMVar_hsa_circ_12323,RMVar_hsa_circ_301474,RMVar_hsa_circ_271331,RMVar_hsa_circ_134108,RMVar_hsa_circ_309794,RMVar_hsa_circ_19815,RMVar_hsa_circ_281278,RMVar_hsa_circ_16016,RMVar_hsa_circ_134109,RMVar_hsa_circ_134110,RMVar_hsa_circ_134111,RMVar_hsa_circ_275281 11471 RMVar_ID_11471 Human_SNP_ID_19549010 A-to-I Human chr1 - 77733282 77733282 77733282 TTGTGTGATCCTCCTGCTTCAGCCTCCTGAGTAGCTGAGACTACAGGCACATGCCACCAAACCTG TTGTGTGATCCTCCTGCTTCAGCCTCCTGAGTGGCTGAGACTACAGGCACATGCCACCAAACCTG T C USP33 Ensembl:ENSG00000077254 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs960175542 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2191,RMVar_hsa_circ_18664,RMVar_hsa_circ_348957,RMVar_hsa_circ_297810,RMVar_hsa_circ_305394,RMVar_hsa_circ_134080,RMVar_hsa_circ_134081,RMVar_hsa_circ_340348,RMVar_hsa_circ_134090,RMVar_hsa_circ_342460,RMVar_hsa_circ_315029,RMVar_hsa_circ_298802,RMVar_hsa_circ_88317,RMVar_hsa_circ_69781,RMVar_hsa_circ_33637,RMVar_hsa_circ_4122,RMVar_hsa_circ_134100,RMVar_hsa_circ_134092,RMVar_hsa_circ_134093,RMVar_hsa_circ_89784,RMVar_hsa_circ_361504,RMVar_hsa_circ_267073,RMVar_hsa_circ_134102,RMVar_hsa_circ_334373,RMVar_hsa_circ_285201,RMVar_hsa_circ_311285,RMVar_hsa_circ_281112,RMVar_hsa_circ_134104,RMVar_hsa_circ_134106,RMVar_hsa_circ_134107,RMVar_hsa_circ_134105,RMVar_hsa_circ_285233,RMVar_hsa_circ_12323,RMVar_hsa_circ_301474,RMVar_hsa_circ_271331,RMVar_hsa_circ_134108,RMVar_hsa_circ_309794,RMVar_hsa_circ_19815,RMVar_hsa_circ_281278,RMVar_hsa_circ_16016,RMVar_hsa_circ_134109,RMVar_hsa_circ_134110,RMVar_hsa_circ_134111,RMVar_hsa_circ_275281 11472 RMVar_ID_11472 Human_SNP_ID_19553022 A-to-I Human chr1 - 77749478 77749478 77749478 ATTTGGGAGGCTGAGACAAGAGAATCGTACGAACCTGGGAGGTGGAGGTTGCAGTGAGCCAAGAT ATTTGGGAGGCTGAGACAAGAGAATCGTACGACCCTGGGAGGTGGAGGTTGCAGTGAGCCAAGAT T G USP33 Ensembl:ENSG00000077254 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404366708 Functional Loss SNV dbSNP153 33..33 33 - - - 11473 RMVar_ID_11473 Human_SNP_ID_19553029 A-to-I Human chr1 - 77749492 77749491 77749493 CTGTAGTCCCAGCTATTTGGGAGGCTGAGACAAGAGAATCGTACGAACCTGGGAGGTGGAGGTTG CTGTAGTCCCAGCTATTTGGGAGGCTGAGAC__GAGAATCGTACGAACCTGGGAGGTGGAGGTTG CTT C USP33 Ensembl:ENSG00000077254 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs796134182 Functional Loss DEL dbSNP153 32..33 33 - - - 11474 RMVar_ID_11474 Human_SNP_ID_19563349 A-to-I Human chr1 + 77789345 77789345 77789345 ATCCTTCCACCTTAGCCTCCCAAGTAGCTTGTACTACAGGAGTGTACCAACACACCCAGCTAATT ATCCTTCCACCTTAGCCTCCCAAGTAGCTTGTGCTACAGGAGTGTACCAACACACCCAGCTAATT A G MIGA1 Ensembl:ENSG00000180488 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1327951543 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_362663 RMVar_hsa_circ_134122,RMVar_hsa_circ_291663,RMVar_hsa_circ_354972,RMVar_hsa_circ_365765,RMVar_hsa_circ_321613,RMVar_hsa_circ_80043,RMVar_hsa_circ_273926,RMVar_hsa_circ_134123,RMVar_hsa_circ_134124,RMVar_hsa_circ_134121 11475 RMVar_ID_11475 Human_SNP_ID_19563359 A-to-I Human chr1 + 77789384 77789384 77789384 GAGTGTACCAACACACCCAGCTAATTTTTTTTATTTTTTGTAGAGACAGGGTTTTACCATCTTGC GAGTGTACCAACACACCCAGCTAATTTTTTTTTTTTTTTGTAGAGACAGGGTTTTACCATCTTGC A T MIGA1 Ensembl:ENSG00000180488 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs61340776 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11111675 RMVar_hsa_circ_134122,RMVar_hsa_circ_291663,RMVar_hsa_circ_354972,RMVar_hsa_circ_365765,RMVar_hsa_circ_321613,RMVar_hsa_circ_80043,RMVar_hsa_circ_273926,RMVar_hsa_circ_134123,RMVar_hsa_circ_134124,RMVar_hsa_circ_134121 11476 RMVar_ID_11476 Human_SNP_ID_19563743 A-to-I Human chr1 + 77790977 77790977 77790977 TCATTTCAAGACTGCTATATAAGGCTGAGAACAGTGGTTTATTCCTGTAATCCCAGCACTTTGGC TCATTTCAAGACTGCTATATAAGGCTGAGAACGGTGGTTTATTCCTGTAATCCCAGCACTTTGGC A G MIGA1 Ensembl:ENSG00000180488 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs888855770 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5866147,Human_RBP_ID_11111722 RMVar_hsa_circ_134122,RMVar_hsa_circ_291663,RMVar_hsa_circ_354972,RMVar_hsa_circ_365765,RMVar_hsa_circ_321613,RMVar_hsa_circ_80043,RMVar_hsa_circ_273926,RMVar_hsa_circ_134123,RMVar_hsa_circ_134124,RMVar_hsa_circ_134121 11477 RMVar_ID_11477 Human_SNP_ID_19563757 A-to-I Human chr1 + 77791033 77791033 77791033 CACTTTGGCTGGCAGGAGGATTGCTTGAGACCAAGAGTTTGAGACCAGCCTAGGCAATATAGTGA CACTTTGGCTGGCAGGAGGATTGCTTGAGACCGAGAGTTTGAGACCAGCCTAGGCAATATAGTGA A G MIGA1 Ensembl:ENSG00000180488 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1018773614 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_134122,RMVar_hsa_circ_291663,RMVar_hsa_circ_354972,RMVar_hsa_circ_365765,RMVar_hsa_circ_321613,RMVar_hsa_circ_80043,RMVar_hsa_circ_273926,RMVar_hsa_circ_134123,RMVar_hsa_circ_134124,RMVar_hsa_circ_134121 11478 RMVar_ID_11478 Human_SNP_ID_19563783 A-to-I Human chr1 + 77791115 77791115 77791115 AATAAAAATAAATATAAGCTGGGCATGGTGGTAGGTGCCTATAGTTCTAGCTGAGGAGGCTGAGA AATAAAAATAAATATAAGCTGGGCATGGTGGTGGGTGCCTATAGTTCTAGCTGAGGAGGCTGAGA A G MIGA1 Ensembl:ENSG00000180488 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1342748577 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_134122,RMVar_hsa_circ_291663,RMVar_hsa_circ_354972,RMVar_hsa_circ_365765,RMVar_hsa_circ_321613,RMVar_hsa_circ_80043,RMVar_hsa_circ_273926,RMVar_hsa_circ_134123,RMVar_hsa_circ_134124,RMVar_hsa_circ_134121 11479 RMVar_ID_11479 Human_SNP_ID_19563786 A-to-I Human chr1 + 77791123 77791123 77791123 TAAATATAAGCTGGGCATGGTGGTAGGTGCCTATAGTTCTAGCTGAGGAGGCTGAGAAGAGAGGA TAAATATAAGCTGGGCATGGTGGTAGGTGCCTGTAGTTCTAGCTGAGGAGGCTGAGAAGAGAGGA A G MIGA1 Ensembl:ENSG00000180488 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223849995 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23413929 RMVar_hsa_circ_134122,RMVar_hsa_circ_291663,RMVar_hsa_circ_354972,RMVar_hsa_circ_365765,RMVar_hsa_circ_321613,RMVar_hsa_circ_80043,RMVar_hsa_circ_273926,RMVar_hsa_circ_134123,RMVar_hsa_circ_134124,RMVar_hsa_circ_134121 11480 RMVar_ID_11480 Human_SNP_ID_19576850 A-to-I Human chr1 + 77846684 77846684 77846684 AATTCAGATACCTCGGCCGGGACTGCTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAG AATTCAGATACCTCGGCCGGGACTGCTGGCTCTCACCTGTAATCCCAGCACTTTGGGAGGCCAAG A T MIGA1 Ensembl:ENSG00000180488 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs376708512 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_98756 RMVar_hsa_circ_53359,RMVar_hsa_circ_134131,RMVar_hsa_circ_365765,RMVar_hsa_circ_80043,RMVar_hsa_circ_291867,RMVar_hsa_circ_134121,RMVar_hsa_circ_364392,RMVar_hsa_circ_281132,RMVar_hsa_circ_267544,RMVar_hsa_circ_21460,RMVar_hsa_circ_134132,RMVar_hsa_circ_134129,RMVar_hsa_circ_134130,RMVar_hsa_circ_134128,RMVar_hsa_circ_87245,RMVar_hsa_circ_134142,RMVar_hsa_circ_66328,RMVar_hsa_circ_134139,RMVar_hsa_circ_327792,RMVar_hsa_circ_329553,RMVar_hsa_circ_23711,RMVar_hsa_circ_36320,RMVar_hsa_circ_134143,RMVar_hsa_circ_134141 11481 RMVar_ID_11481 Human_SNP_ID_19576851 A-to-I Human chr1 + 77846686 77846686 77846686 TTCAGATACCTCGGCCGGGACTGCTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGC TTCAGATACCTCGGCCGGGACTGCTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGC A G MIGA1 Ensembl:ENSG00000180488 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1019595557 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_98756 RMVar_hsa_circ_53359,RMVar_hsa_circ_134131,RMVar_hsa_circ_365765,RMVar_hsa_circ_80043,RMVar_hsa_circ_291867,RMVar_hsa_circ_134121,RMVar_hsa_circ_364392,RMVar_hsa_circ_281132,RMVar_hsa_circ_267544,RMVar_hsa_circ_21460,RMVar_hsa_circ_134132,RMVar_hsa_circ_134129,RMVar_hsa_circ_134130,RMVar_hsa_circ_134128,RMVar_hsa_circ_87245,RMVar_hsa_circ_134142,RMVar_hsa_circ_66328,RMVar_hsa_circ_134139,RMVar_hsa_circ_327792,RMVar_hsa_circ_329553,RMVar_hsa_circ_23711,RMVar_hsa_circ_36320,RMVar_hsa_circ_134143,RMVar_hsa_circ_134141 11482 RMVar_ID_11482 Human_SNP_ID_19584238 A-to-I Human chr1 + 77876179 77876179 77876179 TTAAATTAAATTAATTAGTTGGGTGTGGTGGCATGTGTCTGTGGTCCCAGCTACTTGGGAGGCTG TTAAATTAAATTAATTAGTTGGGTGTGGTGGCGTGTGTCTGTGGTCCCAGCTACTTGGGAGGCTG A G MIGA1 Ensembl:ENSG00000180488 Protein coding 3'UTR GSE100210;GSE99789 HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 29129909,29796672 RNA-Seq:(High) rs536111547 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_46 RMVar_hsa_circ_267544,RMVar_hsa_circ_266070 11483 RMVar_ID_11483 Human_SNP_ID_19584396 A-to-I Human chr1 + 77877044 77877044 77877044 TTGCCTTCTTTTAAGAGATGGGGTCTCGCTCTATTGCCCAGGCTGGAGTGCAGTGTGCTATCATA TTGCCTTCTTTTAAGAGATGGGGTCTCGCTCTGTTGCCCAGGCTGGAGTGCAGTGTGCTATCATA A G MIGA1 Ensembl:ENSG00000180488 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1239023982 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_362742,Human_RBP_ID_4099066,Human_RBP_ID_8169461 RMVar_hsa_circ_267544,RMVar_hsa_circ_266070 11484 RMVar_ID_11484 Human_SNP_ID_19591649 A-to-I Human chr1 + 77906705 77906705 77906705 GAGACAGGGTCTTGCTCTGTTGCCCAGGGTGTAGTGCAGTGGTTCAATCATAGCTCACTGCAGCC GAGACAGGGTCTTGCTCTGTTGCCCAGGGTGTGGTGCAGTGGTTCAATCATAGCTCACTGCAGCC A G NEXN Ensembl:ENSG00000162614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459951056 Functional Loss SNV dbSNP153 33..33 33 - - - 11485 RMVar_ID_11485 Human_SNP_ID_19594308 A-to-I Human chr1 + 77918586 77918586 77918586 TATTCAGAAGGCTGAGGTAGGAGGTTCGCTTGAGCCTGAAAGGTGGAAGTTGCAGTGAGCCAAGA TATTCAGAAGGCTGAGGTAGGAGGTTCGCTTGCGCCTGAAAGGTGGAAGTTGCAGTGAGCCAAGA A C NEXN Ensembl:ENSG00000162614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1363481361 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3933,RMVar_hsa_circ_68508 11486 RMVar_ID_11486 Human_SNP_ID_19595663 A-to-I Human chr1 + 77924219 77924219 77924219 CCCCATCTCTACTAAAAATACAGAAATTAGCCAGGCGTGATGGTGCACACCTGTAGTACCAGCTA CCCCATCTCTACTAAAAATACAGAAATTAGCCGGGCGTGATGGTGCACACCTGTAGTACCAGCTA A G NEXN Ensembl:ENSG00000162614 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1171186918 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3933,RMVar_hsa_circ_68508 11487 RMVar_ID_11487 Human_SNP_ID_19602431 A-to-I Human chr1 - 77950317 77950317 77950317 CATCTCTACAAAAAAAGAGAAAAATGTCAGCTAGGCATGGTGGGCCTGTAGTCCCAGCTACTCTA CATCTCTACAAAAAAAGAGAAAAATGTCAGCTGGGCATGGTGGGCCTGTAGTCCCAGCTACTCTA T C FUBP1 Ensembl:ENSG00000162613 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941771188 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5866854,Human_RBP_ID_11113778 RMVar_hsa_circ_34609,RMVar_hsa_circ_35299,RMVar_hsa_circ_125144,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 11488 RMVar_ID_11488 Human_SNP_ID_19603408 A-to-I Human chr1 - 77954173 77954173 77954173 CCTGACAGCATTGTGGTCAGGACCTGTAATCAACTTAACTTTAATTAAATAGCATCACCATTTTA CCTGACAGCATTGTGGTCAGGACCTGTAATCAGCTTAACTTTAATTAAATAGCATCACCATTTTA T C FUBP1 Ensembl:ENSG00000162613 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965048062 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5866955,Human_RBP_ID_8975344,Human_RBP_ID_11114017,Human_RBP_ID_16977707,Human_RBP_ID_17758298 RMVar_hsa_circ_34609,RMVar_hsa_circ_35299,RMVar_hsa_circ_125144,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 11489 RMVar_ID_11489 Human_SNP_ID_19608333 A-to-I Human chr1 - 77971919 77971919 77971919 CTCACCGTAACCTCCACTTCCTGGGTTCAAGCAGTTCTCCCACCTGAGCCTCCCGAGTAGCTGGG CTCACCGTAACCTCCACTTCCTGGGTTCAAGCGGTTCTCCCACCTGAGCCTCCCGAGTAGCTGGG T C FUBP1 Ensembl:ENSG00000162613 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1250911481 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_134177 11490 RMVar_ID_11490 Human_SNP_ID_19608538 A-to-I Human chr1 - 77972566 77972566 77972566 TTTTGTATTTTTAGTAGAGGTGGTGTTTCACCATGTCAGTCAGGCTGGTCTTGAACTCCTGAACT TTTTGTATTTTTAGTAGAGGTGGTGTTTCACCGTGTCAGTCAGGCTGGTCTTGAACTCCTGAACT T C FUBP1 Ensembl:ENSG00000162613 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1385408192 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11114998 RMVar_hsa_circ_134177 11491 RMVar_ID_11491 Human_SNP_ID_19608802 A-to-I Human chr1 - 77973384 77973384 77973384 AAAATTAGCTGAGCATGGTGGCGGGCGCCTGTAATCCCAGCTACTCGAGAGGCTGAGGCAGGAGA AAAATTAGCTGAGCATGGTGGCGGGCGCCTGTGATCCCAGCTACTCGAGAGGCTGAGGCAGGAGA T C FUBP1 Ensembl:ENSG00000162613 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1438174215 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_134177 11492 RMVar_ID_11492 Human_SNP_ID_19609704 A-to-I Human chr1 - 77976556 77976556 77976556 CTGGGAAGTGGAGGTTGCAGTGAGTGGAGATCACGCTGCTGCACTCCAGCCTGGTCATAGAGCGA CTGGGAAGTGGAGGTTGCAGTGAGTGGAGATCCCGCTGCTGCACTCCAGCCTGGTCATAGAGCGA T G FUBP1 Ensembl:ENSG00000162613 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs778775902 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24769541 RMVar_hsa_circ_134177 11493 RMVar_ID_11493 Human_SNP_ID_19609962 A-to-I Human chr1 - 77977440 77977440 77977440 CCCACTGCAACCTCTGCCTCCCGGCTTCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGG CCCACTGCAACCTCTGCCTCCCGGCTTCAAGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGG T G FUBP1 Ensembl:ENSG00000162613 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs914499671 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_134177 11494 RMVar_ID_11494 Human_SNP_ID_19610882 A-to-I Human chr1 + 77980021 77980021 77980021 TCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACAACAGGCGCCTGCCACCACGTCTGGGCTAATTT TCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCTGCCACCACGTCTGGGCTAATTT A T DNAJB4,GIPC2 Ensembl:ENSG00000162616,Ensembl:ENSG00000137960 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs557813143 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11115308 11495 RMVar_ID_11495 Human_SNP_ID_19611653 A-to-I Human chr1 + 77982637 77982637 77982637 CTGGCCAACATAGTGAAACATCGGCTCTACTAAAAATACAAAAATTAGCTGGGCATGGTAGCGGA CTGGCCAACATAGTGAAACATCGGCTCTACTACAAATACAAAAATTAGCTGGGCATGGTAGCGGA A C DNAJB4,GIPC2 Ensembl:ENSG00000162616,Ensembl:ENSG00000137960 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs938026688 Functional Loss SNV dbSNP153 33..33 33 - - - 11496 RMVar_ID_11496 Human_SNP_ID_19614160 A-to-I Human chr1 + 77992841 77992841 77992841 TGCCTCCCGGGTTCAAGCGATTATCCTGCTTCAGCCTCCCGAGTAGCTGGAATTACAGGCATGTG TGCCTCCCGGGTTCAAGCGATTATCCTGCTTCGGCCTCCCGAGTAGCTGGAATTACAGGCATGTG A G DNAJB4,GIPC2 Ensembl:ENSG00000162616,Ensembl:ENSG00000137960 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910159155 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_89118 11497 RMVar_ID_11497 Human_SNP_ID_19614824 A-to-I Human chr1 + 77995654 77995654 77995654 TGTTTTATTTTTTGTAGATACGAGGTCTCACTATGTTGCTCAGCTGGTCTTGAACTCCTAGACTC TGTTTTATTTTTTGTAGATACGAGGTCTCACTGTGTTGCTCAGCTGGTCTTGAACTCCTAGACTC A G DNAJB4,GIPC2 Ensembl:ENSG00000162616,Ensembl:ENSG00000137960 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs555082259 Functional Loss SNV dbSNP153 33..33 33 - - - 11498 RMVar_ID_11498 Human_SNP_ID_19614935 A-to-I Human chr1 + 77996206 77996206 77996206 ACAGGGTCTTATTGTGTCACTCAGGTTTGAATACAGTGGCATGATCACGGCTCACCTGCAGCCTT ACAGGGTCTTATTGTGTCACTCAGGTTTGAATGCAGTGGCATGATCACGGCTCACCTGCAGCCTT A G DNAJB4,GIPC2 Ensembl:ENSG00000162616,Ensembl:ENSG00000137960 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1467406210 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11115722 11499 RMVar_ID_11499 Human_SNP_ID_19618780 A-to-I Human chr1 + 78012373 78012373 78012373 TTTAGTGGAGGCGGGGTTTCACTGTGTTGGCCAGGCTGGTCTCAAACTCCTGACCTCATGATCTG TTTAGTGGAGGCGGGGTTTCACTGTGTTGGCCGGGCTGGTCTCAAACTCCTGACCTCATGATCTG A G DNAJB4,GIPC2 Ensembl:ENSG00000162616,Ensembl:ENSG00000137960 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs933834039 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120845,RMVar_hsa_circ_134179 11500 RMVar_ID_11500 Human_SNP_ID_19620386 A-to-I Human chr1 + 78018842 78018842 78018842 GTCCAGGAGTTTGAAACCAGCCTGGGCAACATAGTAAGACTCCATCTCTACAAAAAATTTAAAAA GTCCAGGAGTTTGAAACCAGCCTGGGCAACATTGTAAGACTCCATCTCTACAAAAAATTTAAAAA A T GIPC2 Ensembl:ENSG00000137960 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs764898445 Functional Loss SNV dbSNP153 33..33 33 - - - 11501 RMVar_ID_11501 Human_SNP_ID_19621274 A-to-I Human chr1 + 78022678 78022678 78022678 ACTTTGGGAGCCCGACGTGGGCAGATCACTTGAGGTCAGGCCTTCGAGATCAGCCTGGCTAACAT ACTTTGGGAGCCCGACGTGGGCAGATCACTTGCGGTCAGGCCTTCGAGATCAGCCTGGCTAACAT A C GIPC2 Ensembl:ENSG00000137960 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs901041592 Functional Loss SNV dbSNP153 33..33 33 - - - 11502 RMVar_ID_11502 Human_SNP_ID_19621288 A-to-I Human chr1 + 78022741 78022741 78022741 ATTGCAAAACCCCGTCTCTCCTAAAAATACAAAAATTAGCCAGGCGTGGTGGCAGGTGCCTGTAA ATTGCAAAACCCCGTCTCTCCTAAAAATACAACAATTAGCCAGGCGTGGTGGCAGGTGCCTGTAA A C GIPC2 Ensembl:ENSG00000137960 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1022076353 Functional Loss SNV dbSNP153 33..33 33 - - - 11503 RMVar_ID_11503 Human_SNP_ID_19621655 A-to-I Human chr1 + 78024402 78024402 78024402 ATGACTCACTGCAGCCTCGAACTTCTGGGCTCAAGTGATCCTCTGGCCTCAGCCTCCCATGTAGT ATGACTCACTGCAGCCTCGAACTTCTGGGCTCGAGTGATCCTCTGGCCTCAGCCTCCCATGTAGT A G GIPC2 Ensembl:ENSG00000137960 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 29129909,30559470 RNA-Seq:(High) rs1413539028 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1156064 11504 RMVar_ID_11504 Human_SNP_ID_19625929 A-to-I Human chr1 - 78043484 78043484 78043484 TTGCTGCTAGGGCTCTCAAGGAAGAAACAATCATGTATTCAGACATAGACCTGAAGAAGCTGGCT TTGCTGCTAGGGCTCTCAAGGAAGAAACAATCGTGTATTCAGACATAGACCTGAAGAAGCTGGCT T C AC103591.2 Ensembl:ENSG00000213561 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs972338531 Functional Loss SNV dbSNP153 33..33 33 - - - 11505 RMVar_ID_11505 Human_SNP_ID_19795468 A-to-I Human chr1 + 78750087 78750087 78750087 CTGGGATCAAAACTCATGTGGAAAAAGAGGATAGGGAGGCACGTGAGAGGAATGAAATCCGGCAT CTGGGATCAAAACTCATGTGGAAAAAGAGGATGGGGAGGCACGTGAGAGGAATGAAATCCGGCAT A G AC104837.1 Ensembl:ENSG00000235400 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879108768 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18523749 11506 RMVar_ID_11506 Human_SNP_ID_19795475 A-to-I Human chr1 + 78750105 78750105 78750105 TGGAAAAAGAGGATAGGGAGGCACGTGAGAGGAATGAAATCCGGCATGACAGGCGAAAAGAGAGA TGGAAAAAGAGGATAGGGAGGCACGTGAGAGGGATGAAATCCGGCATGACAGGCGAAAAGAGAGA A G AC104837.1 Ensembl:ENSG00000235400 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879107042 Functional Loss SNV dbSNP153 33..33 33 - - - 11507 RMVar_ID_11507 Human_SNP_ID_20601241 A-to-I Human chr1 + 81905350 81905350 81905350 AATCCCCTGACGTCAGGTGATCCACCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAAGCGTGAA AATCCCCTGACGTCAGGTGATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAAGCGTGAA A G ADGRL2 Ensembl:ENSG00000117114 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs944660564 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80421,RMVar_hsa_circ_54923,RMVar_hsa_circ_134189,RMVar_hsa_circ_348145,RMVar_hsa_circ_358453,RMVar_hsa_circ_346698,RMVar_hsa_circ_293247,RMVar_hsa_circ_297021,RMVar_hsa_circ_70474,RMVar_hsa_circ_134195,RMVar_hsa_circ_134191,RMVar_hsa_circ_134194 11508 RMVar_ID_11508 Human_SNP_ID_21074433 A-to-I Human chr1 - 83887095 83887094 83887095 ATCTTTGTGGTAGGTTTCCCTAGAGTTGGCCAAGGGGTTTTGCTGATGTATCAAACAGAAAACAC ATCTTTGTGGTAGGTTTCCCTAGAGTTGGCCA_GGGGTTTTGCTGATGTATCAAACAGAAAACAC CT C TTLL7 Ensembl:ENSG00000137941 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1282331771 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_134211,RMVar_hsa_circ_28930,RMVar_hsa_circ_309001,RMVar_hsa_circ_46359,RMVar_hsa_circ_48769,RMVar_hsa_circ_330286,RMVar_hsa_circ_378263,RMVar_hsa_circ_134209,RMVar_hsa_circ_344106,RMVar_hsa_circ_320666,RMVar_hsa_circ_57782,RMVar_hsa_circ_267957,RMVar_hsa_circ_31885,RMVar_hsa_circ_134213,RMVar_hsa_circ_24409,RMVar_hsa_circ_134214,RMVar_hsa_circ_134212,RMVar_hsa_circ_134210 11509 RMVar_ID_11509 Human_SNP_ID_21081264 A-to-I Human chr1 - 83914460 83914460 83914460 GGGTGTGGTGGCATGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAAGCAGGAGAATTGCTTGAA GGGTGTGGTGGCATGCGCCTGTAGTCCCAGCTGCTCGGGAGGCTGAAGCAGGAGAATTGCTTGAA T C TTLL7 Ensembl:ENSG00000137941 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1321463384 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13019,RMVar_hsa_circ_134211,RMVar_hsa_circ_48769,RMVar_hsa_circ_330286,RMVar_hsa_circ_378263,RMVar_hsa_circ_134209,RMVar_hsa_circ_344106,RMVar_hsa_circ_320666,RMVar_hsa_circ_57782,RMVar_hsa_circ_31885,RMVar_hsa_circ_134213,RMVar_hsa_circ_24409,RMVar_hsa_circ_134214,RMVar_hsa_circ_134212,RMVar_hsa_circ_300668,RMVar_hsa_circ_19210,RMVar_hsa_circ_318396,RMVar_hsa_circ_320100,RMVar_hsa_circ_295189,RMVar_hsa_circ_289058,RMVar_hsa_circ_30072,RMVar_hsa_circ_134217,RMVar_hsa_circ_134219,RMVar_hsa_circ_134218,RMVar_hsa_circ_312150,RMVar_hsa_circ_134215,RMVar_hsa_circ_134216,RMVar_hsa_circ_317802,RMVar_hsa_circ_337765,RMVar_hsa_circ_316097,RMVar_hsa_circ_304908,RMVar_hsa_circ_274784,RMVar_hsa_circ_134235,RMVar_hsa_circ_134226,RMVar_hsa_circ_134228,RMVar_hsa_circ_134229,RMVar_hsa_circ_134230,RMVar_hsa_circ_134227,RMVar_hsa_circ_134225,RMVar_hsa_circ_134232,RMVar_hsa_circ_134231,RMVar_hsa_circ_299889,RMVar_hsa_circ_324204,RMVar_hsa_circ_377835,RMVar_hsa_circ_134233,RMVar_hsa_circ_265964,RMVar_hsa_circ_311850,RMVar_hsa_circ_326528,RMVar_hsa_circ_337917,RMVar_hsa_circ_322672,RMVar_hsa_circ_275043,RMVar_hsa_circ_134234 11510 RMVar_ID_11510 Human_SNP_ID_21088316 A-to-I Human chr1 - 83946176 83946176 83946176 ATGGTGGCGGGCGCCTGCAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATGGTGTGAACCTG ATGGTGGCGGGCGCCTGCAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGTGTGAACCTG T C TTLL7 Ensembl:ENSG00000137941 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1248513371 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1727,RMVar_hsa_circ_378263,RMVar_hsa_circ_320666,RMVar_hsa_circ_31885,RMVar_hsa_circ_134213,RMVar_hsa_circ_134214,RMVar_hsa_circ_300668,RMVar_hsa_circ_289058,RMVar_hsa_circ_134215,RMVar_hsa_circ_134216,RMVar_hsa_circ_304908,RMVar_hsa_circ_274784,RMVar_hsa_circ_134235,RMVar_hsa_circ_134229,RMVar_hsa_circ_134230,RMVar_hsa_circ_134232,RMVar_hsa_circ_324204,RMVar_hsa_circ_322672,RMVar_hsa_circ_275043,RMVar_hsa_circ_318721,RMVar_hsa_circ_316540,RMVar_hsa_circ_134242,RMVar_hsa_circ_134243,RMVar_hsa_circ_296773,RMVar_hsa_circ_12952,RMVar_hsa_circ_294378,RMVar_hsa_circ_324787,RMVar_hsa_circ_134245,RMVar_hsa_circ_325296,RMVar_hsa_circ_134244,RMVar_hsa_circ_267651,RMVar_hsa_circ_134247,RMVar_hsa_circ_134249,RMVar_hsa_circ_53073,RMVar_hsa_circ_319468,RMVar_hsa_circ_134248,RMVar_hsa_circ_329536,RMVar_hsa_circ_134250 11511 RMVar_ID_11511 Human_SNP_ID_21089062 A-to-I Human chr1 - 83949530 83949530 83949530 CGAGGTCAAGAGATTGAGACCTTCCCTGGCCAACATAGTGAAACCCCATCTCTACTAAAAATACA CGAGGTCAAGAGATTGAGACCTTCCCTGGCCAGCATAGTGAAACCCCATCTCTACTAAAAATACA T C TTLL7 Ensembl:ENSG00000137941 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1443127755 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24730471 RMVar_hsa_circ_320666,RMVar_hsa_circ_134214,RMVar_hsa_circ_300668,RMVar_hsa_circ_134215,RMVar_hsa_circ_304908,RMVar_hsa_circ_134230,RMVar_hsa_circ_322672,RMVar_hsa_circ_316540,RMVar_hsa_circ_134243,RMVar_hsa_circ_12952,RMVar_hsa_circ_294378,RMVar_hsa_circ_134244,RMVar_hsa_circ_267651,RMVar_hsa_circ_134249,RMVar_hsa_circ_53073,RMVar_hsa_circ_319468,RMVar_hsa_circ_329536,RMVar_hsa_circ_134251,RMVar_hsa_circ_51931,RMVar_hsa_circ_134250,RMVar_hsa_circ_313175,RMVar_hsa_circ_27125 11512 RMVar_ID_11512 Human_SNP_ID_21089089 A-to-I Human chr1 - 83949607 83949607 83949607 AAAAAACCTCTTCTGGTTGGGCGTGGTGGCTGACACCTGTAATCCCAGCATTTTGGGAGGCCAAG AAAAAACCTCTTCTGGTTGGGCGTGGTGGCTGGCACCTGTAATCCCAGCATTTTGGGAGGCCAAG T C TTLL7 Ensembl:ENSG00000137941 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1376316272 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8975705 RMVar_hsa_circ_320666,RMVar_hsa_circ_134214,RMVar_hsa_circ_300668,RMVar_hsa_circ_134215,RMVar_hsa_circ_304908,RMVar_hsa_circ_134230,RMVar_hsa_circ_322672,RMVar_hsa_circ_316540,RMVar_hsa_circ_134243,RMVar_hsa_circ_12952,RMVar_hsa_circ_294378,RMVar_hsa_circ_134244,RMVar_hsa_circ_267651,RMVar_hsa_circ_134249,RMVar_hsa_circ_53073,RMVar_hsa_circ_319468,RMVar_hsa_circ_329536,RMVar_hsa_circ_134251,RMVar_hsa_circ_51931,RMVar_hsa_circ_134250,RMVar_hsa_circ_313175,RMVar_hsa_circ_27125 11513 RMVar_ID_11513 Human_SNP_ID_21096452 A-to-I Human chr1 - 83983088 83983088 83983088 ACCTCAACTGCTCCACCTGCTTTTGCCTCCCAAACTGCTGGGATTACAGGTGTGAGCCCTTATTG ACCTCAACTGCTCCACCTGCTTTTGCCTCCCAGACTGCTGGGATTACAGGTGTGAGCCCTTATTG T C TTLL7-IT1,TTLL7 Ensembl:ENSG00000233061,Ensembl:ENSG00000137941 lincRNA,Protein coding intron,intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1225209141 Functional Loss SNV dbSNP153 33..33 33 - - - 11514 RMVar_ID_11514 Human_SNP_ID_21096657 A-to-I Human chr1 - 83983905 83983905 83983905 GTTTATAGTTTGTAGAGATGAAGTCTCATTATATTGCCCTGGCCGGTCTCAAACTCTGGGCTCCA GTTTATAGTTTGTAGAGATGAAGTCTCATTATTTTGCCCTGGCCGGTCTCAAACTCTGGGCTCCA T A TTLL7-IT1,TTLL7 Ensembl:ENSG00000233061,Ensembl:ENSG00000137941 lincRNA,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1315974525 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5245461 Human_Splice_Rec_91351 11515 RMVar_ID_11515 Human_SNP_ID_21096744 A-to-I Human chr1 - 83984248 83984248 83984248 TGCTGGCATCTGTTGGTTTTTGACTTTTTGTTAGTTGCCATTCTGACTGATGCGAGATGGTATCT TGCTGGCATCTGTTGGTTTTTGACTTTTTGTTGGTTGCCATTCTGACTGATGCGAGATGGTATCT T C TTLL7-IT1,TTLL7 Ensembl:ENSG00000233061,Ensembl:ENSG00000137941 lincRNA,Protein coding exon,intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs946874919 Functional Loss SNV dbSNP153 33..33 33 - - - 11516 RMVar_ID_11516 Human_SNP_ID_21096875 A-to-I Human chr1 - 83984821 83984821 83984821 GATAGTCCCATAACCCATTTAGTGAGCATAGTACCCAATCAGTAGTTTTTCAGCCCACGTCCCCC GATAGTCCCATAACCCATTTAGTGAGCATAGTTCCCAATCAGTAGTTTTTCAGCCCACGTCCCCC T A TTLL7 Ensembl:ENSG00000137941 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1464423381 Functional Loss SNV dbSNP153 33..33 33 - - - 11517 RMVar_ID_11517 Human_SNP_ID_21097763 A-to-I Human chr1 - 83988489 83988489 83988489 AGAGAACGCTTATACACTACTGGTGAGAATGTAAATTAGTTCAGTCACTGTGGAAAGCAGTTCAG AGAGAACGCTTATACACTACTGGTGAGAATGTGAATTAGTTCAGTCACTGTGGAAAGCAGTTCAG T C TTLL7 Ensembl:ENSG00000137941 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs927906351 Functional Loss SNV dbSNP153 33..33 33 - - - 11518 RMVar_ID_11518 Human_SNP_ID_21098029 A-to-I Human chr1 - 83989612 83989612 83989612 ACCCTGCATAGCTAAAGCAATCCTAAGCAAAAAGAACAAAGCTGGAGGCATCACAATACCTGACT ACCCTGCATAGCTAAAGCAATCCTAAGCAAAAGGAACAAAGCTGGAGGCATCACAATACCTGACT T C TTLL7 Ensembl:ENSG00000137941 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs886572592 Functional Loss SNV dbSNP153 33..33 33 - - - 11519 RMVar_ID_11519 Human_SNP_ID_21120490 A-to-I Human chr1 - 84086124 84086124 84086124 CATTCTTCATGGCCAGCACAGTGGGCACCACCAACACCTCATACTCAATGGCGAGGTCTGTGTGG CATTCTTCATGGCCAGCACAGTGGGCACCACCGACACCTCATACTCAATGGCGAGGTCTGTGTGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1490395800 Functional Loss SNV dbSNP153 33..33 33 - - - 11520 RMVar_ID_11520 Human_SNP_ID_21120492 A-to-I Human chr1 - 84086127 84086127 84086127 CCCCATTCTTCATGGCCAGCACAGTGGGCACCACCAACACCTCATACTCAATGGCGAGGTCTGTG CCCCATTCTTCATGGCCAGCACAGTGGGCACCGCCAACACCTCATACTCAATGGCGAGGTCTGTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1219569099 Functional Loss SNV dbSNP153 33..33 33 - - - 11521 RMVar_ID_11521 Human_SNP_ID_21156759 A-to-I Human chr1 - 84244381 84244381 84244381 TTGATTCACTCCACCTTGTCTGTAGGTTCAATATCAATCTCAGTCTCCTTTCCAGTTAGTGTCTT TTGATTCACTCCACCTTGTCTGTAGGTTCAATGTCAATCTCAGTCTCCTTTCCAGTTAGTGTCTT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879028400 Functional Loss SNV dbSNP153 33..33 33 - - - 11522 RMVar_ID_11522 Human_SNP_ID_21156763 A-to-I Human chr1 - 84244406 84244406 84244406 TCCCTCTTTCTCCTCCACATGCTCCTTGATTCACTCCACCTTGTCTGTAGGTTCAATATCAATCT TCCCTCTTTCTCCTCCACATGCTCCTTGATTCGCTCCACCTTGTCTGTAGGTTCAATATCAATCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879060353 Functional Loss SNV dbSNP153 33..33 33 - - - 11523 RMVar_ID_11523 Human_SNP_ID_21249328 A-to-I Human chr1 - 84648006 84648006 84648006 AGTTACCTAAAAAACTTAGTTTGATCATTTGTACAGGGATTCTGATGACCGAATTACTATAAGTA AGTTACCTAAAAAACTTAGTTTGATCATTTGTGCAGGGATTCTGATGACCGAATTACTATAAGTA T C SSX2IP Ensembl:ENSG00000117155 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978700586 Functional Loss SNV dbSNP153 33..33 33 - - - 11524 RMVar_ID_11524 Human_SNP_ID_21250148 A-to-I Human chr1 - 84651307 84651307 84651307 TTGAAAATTTACATTGAGAATTTCTTTTTTCAAGATGTAGTCTTGCTCTGTCACCCAGGCTGGAG TTGAAAATTTACATTGAGAATTTCTTTTTTCAGGATGTAGTCTTGCTCTGTCACCCAGGCTGGAG T C SSX2IP Ensembl:ENSG00000117155 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1364430721 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50393,RMVar_hsa_circ_267150 11525 RMVar_ID_11525 Human_SNP_ID_21255231 A-to-I Human chr1 - 84671263 84671263 84671263 AGAAGAGTGACAGCAGCTAGACTAAATGTTTAACTGCTGAACTAGTTCCTCAGGTATCCTGGCTC AGAAGAGTGACAGCAGCTAGACTAAATGTTTAGCTGCTGAACTAGTTCCTCAGGTATCCTGGCTC T C SSX2IP Ensembl:ENSG00000117155 Protein coding intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1428617764 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_363694,Human_RBP_ID_4074146,Human_RBP_ID_8976035 Human_Splice_Rec_91942,Human_Splice_Rec_91943,Human_Splice_Rec_91968,Human_Splice_Rec_91969,Human_Splice_Rec_91998,Human_Splice_Rec_91999,Human_Splice_Rec_92055,Human_Splice_Rec_92066,Human_Splice_Rec_92067 RMVar_hsa_circ_50511,RMVar_hsa_circ_50393,RMVar_hsa_circ_49972,RMVar_hsa_circ_282815,RMVar_hsa_circ_19660,RMVar_hsa_circ_134281,RMVar_hsa_circ_267450 11526 RMVar_ID_11526 Human_SNP_ID_21317385 A-to-I Human chr1 - 84931823 84931823 84931823 TGGGGTCTTGTAATCTTTCCCAGGCTGGTCTCAAACTCCTGGGCTCAAGTGATCCTCCAACCTTG TGGGGTCTTGTAATCTTTCCCAGGCTGGTCTCGAACTCCTGGGCTCAAGTGATCCTCCAACCTTG T C MCOLN2 Ensembl:ENSG00000153898 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1419876498 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32177,RMVar_hsa_circ_134285,RMVar_hsa_circ_91702 11527 RMVar_ID_11527 Human_SNP_ID_21320684 A-to-I Human chr1 - 84946038 84946038 84946038 CCACATGTTTAAAATGGGCTACTGCTGAGCACAGTGGCTCACACCTGTAATCCCAGCACTTTGGG CCACATGTTTAAAATGGGCTACTGCTGAGCACTGTGGCTCACACCTGTAATCCCAGCACTTTGGG T A MCOLN2 Ensembl:ENSG00000153898 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs115299606 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_362971,RMVar_hsa_circ_134287 11528 RMVar_ID_11528 Human_SNP_ID_21320685 A-to-I Human chr1 - 84946038 84946038 84946038 CCACATGTTTAAAATGGGCTACTGCTGAGCACAGTGGCTCACACCTGTAATCCCAGCACTTTGGG CCACATGTTTAAAATGGGCTACTGCTGAGCACGGTGGCTCACACCTGTAATCCCAGCACTTTGGG T C MCOLN2 Ensembl:ENSG00000153898 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs115299606 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_362971,RMVar_hsa_circ_134287 11529 RMVar_ID_11529 Human_SNP_ID_21337510 A-to-I Human chr1 - 85016443 85016443 85016443 CGCCTCCCAGGTTCAAGCGATTCTTGTGCCTTAGCCTCCAGAGTAGCTGAAACTACAAGCACACA CGCCTCCCAGGTTCAAGCGATTCTTGTGCCTTGGCCTCCAGAGTAGCTGAAACTACAAGCACACA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1410715481 Functional Loss SNV dbSNP153 33..33 33 - - - 11530 RMVar_ID_11530 Human_SNP_ID_21337539 A-to-I Human chr1 - 85016548 85016546 85016549 AAGCATAAGGGGATTTTTTTTTTTTTTTCTTGAGATAGAGTCTTGCTGTGTTTCCCAGGCTGGAG AAGCATAAGGGGATTTTTTTTTTTTTTTCTT___ATAGAGTCTTGCTGTGTTTCCCAGGCTGGAG TCTC T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1553160894 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_11121363 11531 RMVar_ID_11531 Human_SNP_ID_21339221 A-to-I Human chr1 - 85024140 85024138 85024140 CCTGTTTTTTTTAAGAGACAGGATTTCACTCTATTGCCCAGGCTGGAGTGCAGTGGCGCGATTAT CCTGTTTTTTTTAAGAGACAGGATTTCACTCT__TGCCCAGGCTGGAGTGCAGTGGCGCGATTAT AAT A MCOLN3 Ensembl:ENSG00000055732 Protein coding intron GSE100210;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229 RNA-Seq:(High) rs1015560506 Functional Loss DEL dbSNP153 33..34 33 - - - 11532 RMVar_ID_11532 Human_SNP_ID_21370741 A-to-I Human chr1 - 85163307 85163307 85163307 GGTCAGGAGTTTGAGACCAGCCTGGCCAACATAGTGAAACCCCGCCTCCATTAAAAATACAAAAA GGTCAGGAGTTTGAGACCAGCCTGGCCAACATGGTGAAACCCCGCCTCCATTAAAAATACAAAAA T C SYDE2 Ensembl:ENSG00000097096 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1454646792 Functional Loss SNV dbSNP153 33..33 33 - - - 11533 RMVar_ID_11533 Human_SNP_ID_21374549 A-to-I Human chr1 - 85180633 85180633 85180633 CAGGCTGGAGTGCAATGGCGCAGTCTCAGCTCACTGCAGCCTCCGCCTCCTGGGTTCAAGCAATT CAGGCTGGAGTGCAATGGCGCAGTCTCAGCTCGCTGCAGCCTCCGCCTCCTGGGTTCAAGCAATT T C SYDE2 Ensembl:ENSG00000097096 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs751709447 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_346871,RMVar_hsa_circ_325700,RMVar_hsa_circ_331069,RMVar_hsa_circ_351116 11534 RMVar_ID_11534 Human_SNP_ID_21400433 A-to-I Human chr1 + 85289375 85289375 85289375 CATGTCAGCCAGACTGGTCTCTAACTGACCTCAGGTGATCCGCCCCCCTTGGCCTCCCAAAGTCC CATGTCAGCCAGACTGGTCTCTAACTGACCTCGGGTGATCCGCCCCCCTTGGCCTCCCAAAGTCC A G AL078459.1 Ensembl:ENSG00000223653 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1434863124 Functional Loss SNV dbSNP153 33..33 33 - - - 11535 RMVar_ID_11535 Human_SNP_ID_21468383 A-to-I Human chr1 + 85582494 85582494 85582494 GAAATGTATTGTTCAAACAACTTCATGGTCCCAGTGCTCAAAGACCTGTGGAACTGGTATCTCCA GAAATGTATTGTTCAAACAACTTCATGGTCCCGGTGCTCAAAGACCTGTGGAACTGGTATCTCCA A G CCN1 Ensembl:ENSG00000142871 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1442957353 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22375963 Human_Splice_Rec_92598 RMVar_hsa_circ_134307,RMVar_hsa_circ_334552 11536 RMVar_ID_11536 Human_SNP_ID_21484992 A-to-I Human chr1 - 85651508 85651508 85651508 GAATTGGCTAGGCACAGTGGCTCACAGCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGCAGA GAATTGGCTAGGCACAGTGGCTCACAGCTGTATTCCCAGCACTTTGGGAGGCTGAGGCGGGCAGA T A ZNHIT6 Ensembl:ENSG00000117174 Protein coding 3'UTR GSE38233;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;Bronchiolar epithelium,BERP35T4 cell line - 24183664,31158229 RNA-Seq:(High) rs1259070663 Functional Loss SNV dbSNP153 33..33 33 - - - 11537 RMVar_ID_11537 Human_SNP_ID_21486597 A-to-I Human chr1 - 85658502 85658502 85658502 TTGTAGGCTGGTCATGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGCAGA TTGTAGGCTGGTCATGGTGGCTCACGCCTGTAGTCCCAGCACTTTGGGAGGCCAAGGCAGGCAGA T C ZNHIT6 Ensembl:ENSG00000117174 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1412022948 Functional Loss SNV dbSNP153 33..33 33 - - - 11538 RMVar_ID_11538 Human_SNP_ID_21486652 A-to-I Human chr1 - 85658747 85658747 85658747 CCCACCTCAGCCTCCCGAGTAGCTGTGATTACAGGCATGTGCCACCATGCCGAGCTAATTTTGTA CCCACCTCAGCCTCCCGAGTAGCTGTGATTACTGGCATGTGCCACCATGCCGAGCTAATTTTGTA T A ZNHIT6 Ensembl:ENSG00000117174 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1161515890 Functional Loss SNV dbSNP153 33..33 33 - - - 11539 RMVar_ID_11539 Human_SNP_ID_21653922 A-to-I Human chr1 - 86362752 86362752 86362752 GGGAGGCTGAGGCAGGAGAATCGCTTGAACCCAGGAGGCAGAGGCTGCAGTGAACCCAGATCACA GGGAGGCTGAGGCAGGAGAATCGCTTGAACCCCGGAGGCAGAGGCTGCAGTGAACCCAGATCACA T G ODF2L Ensembl:ENSG00000122417 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1397972223 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8043,RMVar_hsa_circ_83243,RMVar_hsa_circ_104759,RMVar_hsa_circ_87270,RMVar_hsa_circ_134321,RMVar_hsa_circ_77045,RMVar_hsa_circ_134322,RMVar_hsa_circ_134319,RMVar_hsa_circ_134320,RMVar_hsa_circ_365800,RMVar_hsa_circ_281713,RMVar_hsa_circ_22682,RMVar_hsa_circ_18421,RMVar_hsa_circ_35694,RMVar_hsa_circ_134325,RMVar_hsa_circ_134326,RMVar_hsa_circ_57453,RMVar_hsa_circ_318861,RMVar_hsa_circ_8962,RMVar_hsa_circ_66891,RMVar_hsa_circ_353197,RMVar_hsa_circ_362172,RMVar_hsa_circ_304933,RMVar_hsa_circ_134327 11540 RMVar_ID_11540 Human_SNP_ID_21657041 A-to-I Human chr1 - 86376633 86376633 86376633 GAAGAAGGTCCTTTCTTCCTCTGCCTTCTACAATGATTGTAAGTTTCCTGAGATCTTCCCAGCCG GAAGAAGGTCCTTTCTTCCTCTGCCTTCTACAGTGATTGTAAGTTTCCTGAGATCTTCCCAGCCG T C ODF2L Ensembl:ENSG00000122417 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1274599872 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8043,RMVar_hsa_circ_83243,RMVar_hsa_circ_104759,RMVar_hsa_circ_134321,RMVar_hsa_circ_77045,RMVar_hsa_circ_134319,RMVar_hsa_circ_134320,RMVar_hsa_circ_365800,RMVar_hsa_circ_281713,RMVar_hsa_circ_8411,RMVar_hsa_circ_35694,RMVar_hsa_circ_134326,RMVar_hsa_circ_57453,RMVar_hsa_circ_318861,RMVar_hsa_circ_353197,RMVar_hsa_circ_304933,RMVar_hsa_circ_134327,RMVar_hsa_circ_22684,RMVar_hsa_circ_55632,RMVar_hsa_circ_276167,RMVar_hsa_circ_42172,RMVar_hsa_circ_50812,RMVar_hsa_circ_362076,RMVar_hsa_circ_134328,RMVar_hsa_circ_24869,RMVar_hsa_circ_64765,RMVar_hsa_circ_359648,RMVar_hsa_circ_61730 11541 RMVar_ID_11541 Human_SNP_ID_21657574 A-to-I Human chr1 - 86379026 86379024 86379027 GCAAGTAGGGAGGTGCTGCACACTTTTAAACAACCTGATTTCGCAAGAACTCACTCACTATCAGG GCAAGTAGGGAGGTGCTGCACACTTTTAAAC___CTGATTTCGCAAGAACTCACTCACTATCAGG GGTT G ODF2L Ensembl:ENSG00000122417 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs531578668 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_8043,RMVar_hsa_circ_83243,RMVar_hsa_circ_104759,RMVar_hsa_circ_134321,RMVar_hsa_circ_77045,RMVar_hsa_circ_134319,RMVar_hsa_circ_134320,RMVar_hsa_circ_365800,RMVar_hsa_circ_281713,RMVar_hsa_circ_8411,RMVar_hsa_circ_35694,RMVar_hsa_circ_134326,RMVar_hsa_circ_57453,RMVar_hsa_circ_318861,RMVar_hsa_circ_353197,RMVar_hsa_circ_304933,RMVar_hsa_circ_134327,RMVar_hsa_circ_22684,RMVar_hsa_circ_55632,RMVar_hsa_circ_276167,RMVar_hsa_circ_42172,RMVar_hsa_circ_50812,RMVar_hsa_circ_362076,RMVar_hsa_circ_134328,RMVar_hsa_circ_24869,RMVar_hsa_circ_64765,RMVar_hsa_circ_359648,RMVar_hsa_circ_61730 11542 RMVar_ID_11542 Human_SNP_ID_21777894 A-to-I Human chr1 - 86873769 86873769 86873769 TGGCTCACCACAACTTCCACCTTCTGGGTTCAAGTGATTTTCCTACCTCAGCCTCCCAAGTAGCT TGGCTCACCACAACTTCCACCTTCTGGGTTCAGGTGATTTTCCTACCTCAGCCTCCCAAGTAGCT T C SELENOF Ensembl:ENSG00000183291 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1478178583 Functional Loss SNV dbSNP153 33..33 33 - - - 11543 RMVar_ID_11543 Human_SNP_ID_21778012 A-to-I Human chr1 - 86874149 86874149 86874149 CTGACTAGCATGGTGAAACCCCGTCTCTACTAAATATACAAAAAAAAAAAATTAGCAGGGAATCA CTGACTAGCATGGTGAAACCCCGTCTCTACTAGATATACAAAAAAAAAAAATTAGCAGGGAATCA T C SELENOF Ensembl:ENSG00000183291 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1342049491 Functional Loss SNV dbSNP153 33..33 33 - - - 11544 RMVar_ID_11544 Human_SNP_ID_21778025 A-to-I Human chr1 - 86874198 86874190 86874199 TTGGGAGGCCGAGGCAGGCAGATCACGAGGTCAGGCGTTCGAGACCAGCCTGACTAGCATGGTGA TTGGGAGGCCGAGGCAGGCAGATCACGAGGT_________GAGACCAGCCTGACTAGCATGGTGA CGAACGCCTG C SELENOF Ensembl:ENSG00000183291 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1022447630 Functional Loss DEL dbSNP153 32..40 33 - - - Human_RBP_ID_11129812 11545 RMVar_ID_11545 Human_SNP_ID_21778028 A-to-I Human chr1 - 86874198 86874198 86874198 TTGGGAGGCCGAGGCAGGCAGATCACGAGGTCAGGCGTTCGAGACCAGCCTGACTAGCATGGTGA TTGGGAGGCCGAGGCAGGCAGATCACGAGGTCTGGCGTTCGAGACCAGCCTGACTAGCATGGTGA T A SELENOF Ensembl:ENSG00000183291 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893111327 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11129812 11546 RMVar_ID_11546 Human_SNP_ID_21778029 A-to-I Human chr1 - 86874203 86874203 86874203 CCACTTTGGGAGGCCGAGGCAGGCAGATCACGAGGTCAGGCGTTCGAGACCAGCCTGACTAGCAT CCACTTTGGGAGGCCGAGGCAGGCAGATCACGTGGTCAGGCGTTCGAGACCAGCCTGACTAGCAT T A SELENOF Ensembl:ENSG00000183291 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1039987597 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11129812 11547 RMVar_ID_11547 Human_SNP_ID_21778040 A-to-I Human chr1 - 86874242 86874242 86874242 ATTGGTGGCTGGGCAAGGTGGCTTACGCCTGTATTCCCACCACTTTGGGAGGCCGAGGCAGGCAG ATTGGTGGCTGGGCAAGGTGGCTTACGCCTGTGTTCCCACCACTTTGGGAGGCCGAGGCAGGCAG T C SELENOF Ensembl:ENSG00000183291 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1224924097 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11129813 11548 RMVar_ID_11548 Human_SNP_ID_21782506 A-to-I Human chr1 - 86892059 86892059 86892059 GGGCATGGTGGCGGGCTCCTGTAATCTCAGCTACTCCAGAGGCTGAGGCAGGAGAATCGCTTGAA GGGCATGGTGGCGGGCTCCTGTAATCTCAGCTGCTCCAGAGGCTGAGGCAGGAGAATCGCTTGAA T C SELENOF Ensembl:ENSG00000183291 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs964070786 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5873635 RMVar_hsa_circ_28952 11549 RMVar_ID_11549 Human_SNP_ID_21783180 A-to-I Human chr1 - 86894666 86894666 86894666 CCCCCAGCTAATTTTCTATTTTTGTAGAGACAAGGTCTCACCATGTTGCCCAAACTGGTCTTGAA CCCCCAGCTAATTTTCTATTTTTGTAGAGACAGGGTCTCACCATGTTGCCCAAACTGGTCTTGAA T C SELENOF Ensembl:ENSG00000183291 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs369711346 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28952 11550 RMVar_ID_11550 Human_SNP_ID_21783181 A-to-I Human chr1 - 86894666 86894666 86894666 CCCCCAGCTAATTTTCTATTTTTGTAGAGACAAGGTCTCACCATGTTGCCCAAACTGGTCTTGAA CCCCCAGCTAATTTTCTATTTTTGTAGAGACACGGTCTCACCATGTTGCCCAAACTGGTCTTGAA T G SELENOF Ensembl:ENSG00000183291 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs369711346 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28952 11551 RMVar_ID_11551 Human_SNP_ID_21783188 A-to-I Human chr1 - 86894673 86894673 86894673 GTCATCACCCCCAGCTAATTTTCTATTTTTGTAGAGACAAGGTCTCACCATGTTGCCCAAACTGG GTCATCACCCCCAGCTAATTTTCTATTTTTGTGGAGACAAGGTCTCACCATGTTGCCCAAACTGG T C SELENOF Ensembl:ENSG00000183291 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1257114164 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28952 11552 RMVar_ID_11552 Human_SNP_ID_21783220 A-to-I Human chr1 - 86894831 86894831 86894831 GTTGTTGTTGTTGTTGTTGTTGTTTTAGAGATAGGGTTTCCCTCTGTCACCCAAGCTAGAATGTA GTTGTTGTTGTTGTTGTTGTTGTTTTAGAGATTGGGTTTCCCTCTGTCACCCAAGCTAGAATGTA T A SELENOF Ensembl:ENSG00000183291 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913504444 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2169707,Human_RBP_ID_3324096,Human_RBP_ID_11130588,Human_RBP_ID_26591582 RMVar_hsa_circ_28952 11553 RMVar_ID_11553 Human_SNP_ID_21785193 A-to-I Human chr1 - 86901033 86901033 86901033 CAAAAATTAGCCAAGTGTGGTGGTTTACGCCTATAGTACCAGCTACTCAGGAGCCTGAGGTGGAA CAAAAATTAGCCAAGTGTGGTGGTTTACGCCTGTAGTACCAGCTACTCAGGAGCCTGAGGTGGAA T C SELENOF Ensembl:ENSG00000183291 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1333210557 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28952 11554 RMVar_ID_11554 Human_SNP_ID_21796853 A-to-I Human chr1 + 86949490 86949488 86949491 AGAAATAGAGGCTTAAGCAGGAGAATCACTTGAGCCCAAAAGGCAGAGGTTGCAGTGAGCTGAGA AGAAATAGAGGCTTAAGCAGGAGAATCACTT___CCCAAAAGGCAGAGGTTGCAGTGAGCTGAGA TGAG T HS2ST1 Ensembl:ENSG00000153936 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1268586822 Functional Loss DEL dbSNP153 32..34 33 - - - 11555 RMVar_ID_11555 Human_SNP_ID_21802175 A-to-I Human chr1 + 86970540 86970540 86970540 GTTGTGCCTCAGCCTCCCAAGTTGCTGGGACTACAGGCGTGCACCACCATGCTTGGCAAATTTTT GTTGTGCCTCAGCCTCCCAAGTTGCTGGGACTGCAGGCGTGCACCACCATGCTTGGCAAATTTTT A G HS2ST1 Ensembl:ENSG00000153936 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559311243 Functional Loss SNV dbSNP153 33..33 33 - - - 11556 RMVar_ID_11556 Human_SNP_ID_21820333 A-to-I Human chr1 - 87046116 87046116 87046116 GGCAGCTCTGTTATCTAAAGCATTCATAACCAATATAAACTGTCAAAAATATGCCACATTATAGT GGCAGCTCTGTTATCTAAAGCATTCATAACCAGTATAAACTGTCAAAAATATGCCACATTATAGT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879242073 Functional Loss SNV dbSNP153 33..33 33 - - - 11557 RMVar_ID_11557 Human_SNP_ID_21820384 A-to-I Human chr1 + 87046254 87046254 87046254 GACAAGTAACTACTATCAAAGAGGGTGTGACCAAGTGTTACGAATGTCATCCTAAGCCAACCCAG GACAAGTAACTACTATCAAAGAGGGTGTGACCGAGTGTTACGAATGTCATCCTAAGCCAACCCAG A G AC093155.1,HS2ST1,AC093155.3 Ensembl:ENSG00000225568,Ensembl:ENSG00000153936,Ensembl:ENSG00000267561 Pseudogene,Protein coding,Protein coding exon,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1175531843 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18236041 Human_miRNA_ID_1862305 11558 RMVar_ID_11558 Human_SNP_ID_21820388 A-to-I Human chr1 + 87046264 87046264 87046264 TACTATCAAAGAGGGTGTGACCAAGTGTTACGAATGTCATCCTAAGCCAACCCAGAGAACCTCTC TACTATCAAAGAGGGTGTGACCAAGTGTTACGCATGTCATCCTAAGCCAACCCAGAGAACCTCTC A C AC093155.1,HS2ST1,AC093155.3 Ensembl:ENSG00000225568,Ensembl:ENSG00000153936,Ensembl:ENSG00000267561 Pseudogene,Protein coding,Protein coding exon,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1472801596 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1900889 11559 RMVar_ID_11559 Human_SNP_ID_21820416 A-to-I Human chr1 + 87046410 87046410 87046410 AGAGCTGACCCTGAAGCTGCCTGGGAACCAACAGAAGCCAAAGCCAGAGCTAGAACATTCTAATA AGAGCTGACCCTGAAGCTGCCTGGGAACCAACGGAAGCCAAAGCCAGAGCTAGAACATTCTAATA A G AC093155.1,HS2ST1,AC093155.3 Ensembl:ENSG00000225568,Ensembl:ENSG00000153936,Ensembl:ENSG00000267561 Pseudogene,Protein coding,Protein coding exon,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879023928 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5889943,Human_RBP_ID_8242589,Human_RBP_ID_17340033,Human_RBP_ID_17456709,Human_RBP_ID_17586671,Human_RBP_ID_26383775 11560 RMVar_ID_11560 Human_SNP_ID_21820418 A-to-I Human chr1 + 87046417 87046417 87046417 ACCCTGAAGCTGCCTGGGAACCAACAGAAGCCAAAGCCAGAGCTAGAACATTCTAATAAAGAAGG ACCCTGAAGCTGCCTGGGAACCAACAGAAGCCGAAGCCAGAGCTAGAACATTCTAATAAAGAAGG A G AC093155.1,HS2ST1,AC093155.3 Ensembl:ENSG00000225568,Ensembl:ENSG00000153936,Ensembl:ENSG00000267561 Pseudogene,Protein coding,Protein coding exon,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879200517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8242589,Human_RBP_ID_17586671,Human_RBP_ID_26383775 11561 RMVar_ID_11561 Human_SNP_ID_22203956 A-to-I Human chr1 + 88710818 88710818 88710818 TTTCATTATTTTGTATATACCCGAAGGAATATAAATCATTCTATTATAAAGACACATTCACGCAT TTTCATTATTTTGTATATACCCGAAGGAATATGAATCATTCTATTATAAAGACACATTCACGCAT A G PKN2 Ensembl:ENSG00000065243 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1260811869 Functional Loss SNV dbSNP153 33..33 33 - - - 11562 RMVar_ID_11562 Human_SNP_ID_22203985 A-to-I Human chr1 + 88710916 88710916 88710916 ACATGGAATCAACCTAAATGCCCACCAATAATAGACTGGATACAGGAAAGGTGGTACATACACAT ACATGGAATCAACCTAAATGCCCACCAATAATTGACTGGATACAGGAAAGGTGGTACATACACAT A T PKN2 Ensembl:ENSG00000065243 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs746230776 Functional Loss SNV dbSNP153 33..33 33 - - - 11563 RMVar_ID_11563 Human_SNP_ID_22216272 A-to-I Human chr1 + 88761498 88761498 88761498 CTAACTACTCACCCCAAATGAAATTTGAGACTAGGCCTGGTGGCTCACACCTGTATACCTAGAAC CTAACTACTCACCCCAAATGAAATTTGAGACTCGGCCTGGTGGCTCACACCTGTATACCTAGAAC A C PKN2 Ensembl:ENSG00000065243 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs533721550 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5876658,Human_RBP_ID_11137804 RMVar_hsa_circ_2022,RMVar_hsa_circ_74020,RMVar_hsa_circ_315897,RMVar_hsa_circ_350758,RMVar_hsa_circ_360043,RMVar_hsa_circ_106564,RMVar_hsa_circ_271988,RMVar_hsa_circ_74591,RMVar_hsa_circ_134360,RMVar_hsa_circ_25425,RMVar_hsa_circ_48397,RMVar_hsa_circ_134361,RMVar_hsa_circ_326831,RMVar_hsa_circ_134359,RMVar_hsa_circ_372436,RMVar_hsa_circ_336268,RMVar_hsa_circ_65014,RMVar_hsa_circ_299589,RMVar_hsa_circ_25621,RMVar_hsa_circ_134364,RMVar_hsa_circ_134365,RMVar_hsa_circ_134366 11564 RMVar_ID_11564 Human_SNP_ID_22217125 A-to-I Human chr1 + 88765022 88765022 88765022 TTGGCTCACTGCAACCTCTGCCTCCCAAATTCAAGCGATTCTTCTGCCTCAGCCTGCCTCCTGTG TTGGCTCACTGCAACCTCTGCCTCCCAAATTCGAGCGATTCTTCTGCCTCAGCCTGCCTCCTGTG A G PKN2 Ensembl:ENSG00000065243 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs553168256 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2022,RMVar_hsa_circ_74020,RMVar_hsa_circ_315897,RMVar_hsa_circ_350758,RMVar_hsa_circ_360043,RMVar_hsa_circ_106564,RMVar_hsa_circ_271988,RMVar_hsa_circ_74591,RMVar_hsa_circ_134360,RMVar_hsa_circ_25425,RMVar_hsa_circ_48397,RMVar_hsa_circ_134361,RMVar_hsa_circ_326831,RMVar_hsa_circ_134359,RMVar_hsa_circ_372436,RMVar_hsa_circ_336268,RMVar_hsa_circ_65014,RMVar_hsa_circ_299589,RMVar_hsa_circ_25621,RMVar_hsa_circ_134364,RMVar_hsa_circ_134365,RMVar_hsa_circ_134366 11565 RMVar_ID_11565 Human_SNP_ID_22220055 A-to-I Human chr1 + 88776462 88776462 88776462 TTTTTTTCCAGCACTTAAAAAAATGTCCAACTAGGCACAGTGGCTCACACCTATAATCCCAGCAC TTTTTTTCCAGCACTTAAAAAAATGTCCAACTGGGCACAGTGGCTCACACCTATAATCCCAGCAC A G PKN2 Ensembl:ENSG00000065243 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs778850592 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2022,RMVar_hsa_circ_74020,RMVar_hsa_circ_350758,RMVar_hsa_circ_360043,RMVar_hsa_circ_106564,RMVar_hsa_circ_271988,RMVar_hsa_circ_74591,RMVar_hsa_circ_134360,RMVar_hsa_circ_25425,RMVar_hsa_circ_326831,RMVar_hsa_circ_134359,RMVar_hsa_circ_372436,RMVar_hsa_circ_336268,RMVar_hsa_circ_65014,RMVar_hsa_circ_25621,RMVar_hsa_circ_2496,RMVar_hsa_circ_134370,RMVar_hsa_circ_121416,RMVar_hsa_circ_282264,RMVar_hsa_circ_134365,RMVar_hsa_circ_134366,RMVar_hsa_circ_352307,RMVar_hsa_circ_371037,RMVar_hsa_circ_372169,RMVar_hsa_circ_334874,RMVar_hsa_circ_278606,RMVar_hsa_circ_126001,RMVar_hsa_circ_134372,RMVar_hsa_circ_134374,RMVar_hsa_circ_93447,RMVar_hsa_circ_134373,RMVar_hsa_circ_134371,RMVar_hsa_circ_90962,RMVar_hsa_circ_134368,RMVar_hsa_circ_134369,RMVar_hsa_circ_355982,RMVar_hsa_circ_134367,RMVar_hsa_circ_340344,RMVar_hsa_circ_286608,RMVar_hsa_circ_46414,RMVar_hsa_circ_56589,RMVar_hsa_circ_134377,RMVar_hsa_circ_314257,RMVar_hsa_circ_334056,RMVar_hsa_circ_35408,RMVar_hsa_circ_134379,RMVar_hsa_circ_134380,RMVar_hsa_circ_134378 11566 RMVar_ID_11566 Human_SNP_ID_22222945 A-to-I Human chr1 + 88788625 88788625 88788625 GTACCACCACGCCTGTCTAATTTTGTATTTTTAGTAGAGATGGGGGTTCTCCATGTTGGTCAGGC GTACCACCACGCCTGTCTAATTTTGTATTTTTGGTAGAGATGGGGGTTCTCCATGTTGGTCAGGC A G PKN2 Ensembl:ENSG00000065243 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1472846722 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2022,RMVar_hsa_circ_74020,RMVar_hsa_circ_350758,RMVar_hsa_circ_106564,RMVar_hsa_circ_25425,RMVar_hsa_circ_326831,RMVar_hsa_circ_134359,RMVar_hsa_circ_65014,RMVar_hsa_circ_25621,RMVar_hsa_circ_2496,RMVar_hsa_circ_134370,RMVar_hsa_circ_121416,RMVar_hsa_circ_282264,RMVar_hsa_circ_352307,RMVar_hsa_circ_371037,RMVar_hsa_circ_334874,RMVar_hsa_circ_126001,RMVar_hsa_circ_134372,RMVar_hsa_circ_93447,RMVar_hsa_circ_134371,RMVar_hsa_circ_90962,RMVar_hsa_circ_134368,RMVar_hsa_circ_134369,RMVar_hsa_circ_355982,RMVar_hsa_circ_134367,RMVar_hsa_circ_340344,RMVar_hsa_circ_46414,RMVar_hsa_circ_56589,RMVar_hsa_circ_134377,RMVar_hsa_circ_334056,RMVar_hsa_circ_35408,RMVar_hsa_circ_134389,RMVar_hsa_circ_321237,RMVar_hsa_circ_134379,RMVar_hsa_circ_134380,RMVar_hsa_circ_335943,RMVar_hsa_circ_30274,RMVar_hsa_circ_134382,RMVar_hsa_circ_134383,RMVar_hsa_circ_266326,RMVar_hsa_circ_283113,RMVar_hsa_circ_342272,RMVar_hsa_circ_349055,RMVar_hsa_circ_302495,RMVar_hsa_circ_278138,RMVar_hsa_circ_103156,RMVar_hsa_circ_134385,RMVar_hsa_circ_134387,RMVar_hsa_circ_134388,RMVar_hsa_circ_134386,RMVar_hsa_circ_134384 11567 RMVar_ID_11567 Human_SNP_ID_22222957 A-to-I Human chr1 + 88788683 88788683 88788683 GTCAGGCTGGTCTTGAACTCCCAACCTCAGGTAATCCACCCACCTCGGCCTCCCAAAGTGCTGGG GTCAGGCTGGTCTTGAACTCCCAACCTCAGGTGATCCACCCACCTCGGCCTCCCAAAGTGCTGGG A G PKN2 Ensembl:ENSG00000065243 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474741612 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2022,RMVar_hsa_circ_74020,RMVar_hsa_circ_350758,RMVar_hsa_circ_106564,RMVar_hsa_circ_25425,RMVar_hsa_circ_326831,RMVar_hsa_circ_134359,RMVar_hsa_circ_65014,RMVar_hsa_circ_25621,RMVar_hsa_circ_2496,RMVar_hsa_circ_134370,RMVar_hsa_circ_121416,RMVar_hsa_circ_282264,RMVar_hsa_circ_352307,RMVar_hsa_circ_371037,RMVar_hsa_circ_334874,RMVar_hsa_circ_126001,RMVar_hsa_circ_134372,RMVar_hsa_circ_93447,RMVar_hsa_circ_134371,RMVar_hsa_circ_90962,RMVar_hsa_circ_134368,RMVar_hsa_circ_134369,RMVar_hsa_circ_355982,RMVar_hsa_circ_134367,RMVar_hsa_circ_340344,RMVar_hsa_circ_46414,RMVar_hsa_circ_56589,RMVar_hsa_circ_134377,RMVar_hsa_circ_334056,RMVar_hsa_circ_35408,RMVar_hsa_circ_134389,RMVar_hsa_circ_321237,RMVar_hsa_circ_134379,RMVar_hsa_circ_134380,RMVar_hsa_circ_335943,RMVar_hsa_circ_30274,RMVar_hsa_circ_134382,RMVar_hsa_circ_134383,RMVar_hsa_circ_266326,RMVar_hsa_circ_283113,RMVar_hsa_circ_342272,RMVar_hsa_circ_349055,RMVar_hsa_circ_302495,RMVar_hsa_circ_278138,RMVar_hsa_circ_103156,RMVar_hsa_circ_134385,RMVar_hsa_circ_134387,RMVar_hsa_circ_134388,RMVar_hsa_circ_134386,RMVar_hsa_circ_134384 11568 RMVar_ID_11568 Human_SNP_ID_22226354 A-to-I Human chr1 + 88802540 88802540 88802540 AGAAATGGGGTTTCACCATGTTGGCCGTTGCTAGTCTCGAACTCCTGACCTCAAGTGATTCACCC AGAAATGGGGTTTCACCATGTTGGCCGTTGCTGGTCTCGAACTCCTGACCTCAAGTGATTCACCC A G PKN2 Ensembl:ENSG00000065243 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1290183303 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11138788 RMVar_hsa_circ_2022,RMVar_hsa_circ_74020,RMVar_hsa_circ_350758,RMVar_hsa_circ_106564,RMVar_hsa_circ_25425,RMVar_hsa_circ_326831,RMVar_hsa_circ_134359,RMVar_hsa_circ_65014,RMVar_hsa_circ_25621,RMVar_hsa_circ_2496,RMVar_hsa_circ_134370,RMVar_hsa_circ_121416,RMVar_hsa_circ_282264,RMVar_hsa_circ_352307,RMVar_hsa_circ_371037,RMVar_hsa_circ_334874,RMVar_hsa_circ_126001,RMVar_hsa_circ_134372,RMVar_hsa_circ_93447,RMVar_hsa_circ_134371,RMVar_hsa_circ_90962,RMVar_hsa_circ_134368,RMVar_hsa_circ_134369,RMVar_hsa_circ_355982,RMVar_hsa_circ_134367,RMVar_hsa_circ_340344,RMVar_hsa_circ_46414,RMVar_hsa_circ_56589,RMVar_hsa_circ_134377,RMVar_hsa_circ_334056,RMVar_hsa_circ_35408,RMVar_hsa_circ_321237,RMVar_hsa_circ_134379,RMVar_hsa_circ_134380,RMVar_hsa_circ_335943,RMVar_hsa_circ_30274,RMVar_hsa_circ_134383,RMVar_hsa_circ_266326,RMVar_hsa_circ_283113,RMVar_hsa_circ_342272,RMVar_hsa_circ_349055,RMVar_hsa_circ_302495,RMVar_hsa_circ_278138,RMVar_hsa_circ_103156,RMVar_hsa_circ_134385,RMVar_hsa_circ_134387,RMVar_hsa_circ_134388,RMVar_hsa_circ_134386,RMVar_hsa_circ_134384 11569 RMVar_ID_11569 Human_SNP_ID_22231466 A-to-I Human chr1 + 88823037 88823037 88823037 GTCTAGGAGTTTGAGACCCGCCTGGGCAACATAGTGATATTCTGTCTCTACAAAAAAATAACAAA GTCTAGGAGTTTGAGACCCGCCTGGGCAACATGGTGATATTCTGTCTCTACAAAAAAATAACAAA A G PKN2 Ensembl:ENSG00000065243 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs148718143 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106564,RMVar_hsa_circ_134359,RMVar_hsa_circ_65014,RMVar_hsa_circ_371037,RMVar_hsa_circ_134367,RMVar_hsa_circ_266326,RMVar_hsa_circ_103156,RMVar_hsa_circ_134384,RMVar_hsa_circ_55497 11570 RMVar_ID_11570 Human_SNP_ID_22239386 A-to-I Human chr1 - 88855549 88855549 88855549 CAGCAGTTCAAGACCAGCCTGGCCAACATGGCAAAACCCCATCTCTACTAAAAATACAAAAATCA CAGCAGTTCAAGACCAGCCTGGCCAACATGGCGAAACCCCATCTCTACTAAAAATACAAAAATCA T C GTF2B Ensembl:ENSG00000137947 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1032555122 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_134396,RMVar_hsa_circ_134397,RMVar_hsa_circ_134398 11571 RMVar_ID_11571 Human_SNP_ID_22239464 A-to-I Human chr1 - 88855859 88855859 88855859 TAAACTAGGTGCGGTGACCAGCCTCCTGGCCAACATGGCAAAACCCTGTCTCTACTAAAAACACA TAAACTAGGTGCGGTGACCAGCCTCCTGGCCAGCATGGCAAAACCCTGTCTCTACTAAAAACACA T C GTF2B Ensembl:ENSG00000137947 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1446130868 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_134396,RMVar_hsa_circ_134397,RMVar_hsa_circ_134398 11572 RMVar_ID_11572 Human_SNP_ID_22242172 A-to-I Human chr1 - 88866118 88866118 88866118 GGCTCATGTGATTTTCCTGCTTAAGCCTCCCAAAGTGCTAAGATTACAGGTGTGAACCACCATGC GGCTCATGTGATTTTCCTGCTTAAGCCTCCCAGAGTGCTAAGATTACAGGTGTGAACCACCATGC T C GTF2B Ensembl:ENSG00000137947 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs932840946 Functional Loss SNV dbSNP153 33..33 33 - - - 11573 RMVar_ID_11573 Human_SNP_ID_22246734 A-to-I Human chr1 - 88883497 88883497 88883497 GTTGCCCAGACTAGTCTTGAACCCTGGCCTCAAGTGATCTTTTTGCCTTGATCTCCCAAAGTGCT GTTGCCCAGACTAGTCTTGAACCCTGGCCTCAGGTGATCTTTTTGCCTTGATCTCCCAAAGTGCT T C GTF2B Ensembl:ENSG00000137947 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1465160288 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11140273 11574 RMVar_ID_11574 Human_SNP_ID_22264733 A-to-I Human chr1 - 88959034 88959034 88959034 GACTCAAGCGATCCTCCTGCCCTGGCCTCCCAAAGGGCTGTGATTACAGGCATAAGCCATAGAAC GACTCAAGCGATCCTCCTGCCCTGGCCTCCCAGAGGGCTGTGATTACAGGCATAAGCCATAGAAC T C KYAT3 Ensembl:ENSG00000137944 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749587395 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4129,RMVar_hsa_circ_73866,RMVar_hsa_circ_265504,RMVar_hsa_circ_134401,RMVar_hsa_circ_301187,RMVar_hsa_circ_357905,RMVar_hsa_circ_58424,RMVar_hsa_circ_134403,RMVar_hsa_circ_335094,RMVar_hsa_circ_296444,RMVar_hsa_circ_23721,RMVar_hsa_circ_360769,RMVar_hsa_circ_39045,RMVar_hsa_circ_36762,RMVar_hsa_circ_360777,RMVar_hsa_circ_134406 11575 RMVar_ID_11575 Human_SNP_ID_22290013 A-to-I Human chr1 - 89060326 89060326 89060326 AATCCCCATCGCTGGTCTCCTCTCTCCCTTGCAGGCTTCTCTCTGGGCTCCACGGTGCAGTCTCA AATCCCCATCGCTGGTCTCCTCTCTCCCTTGCCGGCTTCTCTCTGGGCTCCACGGTGCAGTCTCA T G GBP1 Ensembl:ENSG00000117228 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1356542986 Functional Loss SNV dbSNP153 33..33 33 - - - 11576 RMVar_ID_11576 Human_SNP_ID_22304867 A-to-I Human chr1 - 89121985 89121985 89121985 TGCTTTCCATTTCATCTTTTTCCTTGCACACAAGGGAACAACACCCTGGACATGGCTCCAGAGAT TGCTTTCCATTTCATCTTTTTCCTTGCACACAGGGGAACAACACCCTGGACATGGCTCCAGAGAT T C GBP2 Ensembl:ENSG00000162645 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1239545259 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57737 11577 RMVar_ID_11577 Human_SNP_ID_22319759 A-to-I Human chr1 - 89182706 89182704 89182707 GGAGGCCGAGACGGGTGGATCACGAGGTCAGGAGATCGAGACCATCCTGGCTAACACGGTGAAAC GGAGGCCGAGACGGGTGGATCACGAGGTCAG___ATCGAGACCATCCTGGCTAACACGGTGAAAC TCTC T GBP4 Ensembl:ENSG00000162654 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1245914837 Functional Loss DEL dbSNP153 32..34 33 - - - 11578 RMVar_ID_11578 Human_SNP_ID_22319760 A-to-I Human chr1 - 89182709 89182709 89182709 TTGGGAGGCCGAGACGGGTGGATCACGAGGTCAGGAGATCGAGACCATCCTGGCTAACACGGTGA TTGGGAGGCCGAGACGGGTGGATCACGAGGTCGGGAGATCGAGACCATCCTGGCTAACACGGTGA T C GBP4 Ensembl:ENSG00000162654 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs375707680 Functional Loss SNV dbSNP153 33..33 33 - - - 11579 RMVar_ID_11579 Human_SNP_ID_22319966 A-to-I Human chr1 - 89183696 89183696 89183696 TTTTGTATTTGTTTGTAGAGATGTGTTTTTCCATGTTGCCCAAGCTGGTCTTGAACTACTGAGCT TTTTGTATTTGTTTGTAGAGATGTGTTTTTCCGTGTTGCCCAAGCTGGTCTTGAACTACTGAGCT T C GBP4 Ensembl:ENSG00000162654 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs964904687 Functional Loss SNV dbSNP153 33..33 33 - - - 11580 RMVar_ID_11580 Human_SNP_ID_22319987 A-to-I Human chr1 - 89183804 89183804 89183804 ACAAACATGGGTCATTGTAGCCTCAACCTCCCAGGCTCAAGCAGTCCTTTCACCTCAACCCCCCA ACAAACATGGGTCATTGTAGCCTCAACCTCCCGGGCTCAAGCAGTCCTTTCACCTCAACCCCCCA T C GBP4 Ensembl:ENSG00000162654 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1223476015 Functional Loss SNV dbSNP153 33..33 33 - - - 11581 RMVar_ID_11581 Human_SNP_ID_22369629 A-to-I Human chr1 + 89387853 89387853 89387853 TACACAGGAGGATGAGGCAGGAAAATCACTTGAACCTGGGAGGTGGAGGTTGCAGTGAGCCGAGA TACACAGGAGGATGAGGCAGGAAAATCACTTGTACCTGGGAGGTGGAGGTTGCAGTGAGCCGAGA A T GBP6 Ensembl:ENSG00000183347 Protein coding 3'UTR GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1412098604 Functional Loss SNV dbSNP153 33..33 33 - - - 11582 RMVar_ID_11582 Human_SNP_ID_22428257 A-to-I Human chr1 + 89643169 89643169 89643169 GCCAGAGTGCAATGGCACAATCTTGGCTCACTACAACCTCTACCTCTGAGACTCAAGCCATCCTT GCCAGAGTGCAATGGCACAATCTTGGCTCACTGCAACCTCTACCTCTGAGACTCAAGCCATCCTT A G AC093423.2,AC093423.3,LRRC8C Ensembl:ENSG00000230735,Ensembl:ENSG00000271949,Ensembl:ENSG00000171488 lincRNA,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1166015529 Functional Loss SNV dbSNP153 33..33 33 - - - 11583 RMVar_ID_11583 Human_SNP_ID_22445602 A-to-I Human chr1 + 89719142 89719142 89719142 GAGGATCTCCCCCTGCCCAAAGGAATTTTTTTATCAGAATACCTTGAAAGGGGGGTATATAAATT GAGGATCTCCCCCTGCCCAAAGGAATTTTTTTGTCAGAATACCTTGAAAGGGGGGTATATAAATT A G AC093423.3,LRRC8C Ensembl:ENSG00000271949,Ensembl:ENSG00000171488 Protein coding,Protein coding intron,intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs551710282 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_134423,RMVar_hsa_circ_112931 11584 RMVar_ID_11584 Human_SNP_ID_22475544 A-to-I Human chr1 + 89846000 89846000 89846000 ATGGGGTTTATCCATGTTGGTCAGACTGGTCTAGAACTCCTCACCCCATGATCCACCCGCCTCGG ATGGGGTTTATCCATGTTGGTCAGACTGGTCTGGAACTCCTCACCCCATGATCCACCCGCCTCGG A G AC093423.3,LRRC8D Ensembl:ENSG00000271949,Ensembl:ENSG00000171492 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348632459 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8321255,Human_RBP_ID_11141922 RMVar_hsa_circ_134426 11585 RMVar_ID_11585 Human_SNP_ID_595683661 A-to-I Human chr16 - 15007453 15007453 15007453 ATAGTCATGCTCGGCTGGGCGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGT ATAGTCATGCTCGGCTGGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGT T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1018577842 Functional Loss SNV dbSNP153 33..33 33 - - - 11586 RMVar_ID_11586 Human_SNP_ID_595685356 A-to-I Human chr16 - 15012986 15012986 15012986 TTTTGTATTTTTAGTGGAAACGGGGTTTCACCATGTTAGCCAGGATGTCTTGATCTCCTGACCTC TTTTGTATTTTTAGTGGAAACGGGGTTTCACCGTGTTAGCCAGGATGTCTTGATCTCCTGACCTC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1454194049 Functional Loss SNV dbSNP153 33..33 33 - - - 11587 RMVar_ID_11587 Human_SNP_ID_595685809 A-to-I Human chr16 + 15014132 15014132 15014132 AGGAGGCCGAGGCAGGAGAATAGCTTGAACCCAGGAGGCTGAGATTGCAGTGAGCCGAGATTGCG AGGAGGCCGAGGCAGGAGAATAGCTTGAACCCGGGAGGCTGAGATTGCAGTGAGCCGAGATTGCG A G PDXDC1 Ensembl:ENSG00000179889 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1271285058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12671982 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_125777,RMVar_hsa_circ_176498,RMVar_hsa_circ_5646,RMVar_hsa_circ_69488,RMVar_hsa_circ_321402,RMVar_hsa_circ_346116,RMVar_hsa_circ_82502,RMVar_hsa_circ_39291,RMVar_hsa_circ_176503,RMVar_hsa_circ_176504 11588 RMVar_ID_11588 Human_SNP_ID_595686139 A-to-I Human chr16 + 15015015 15015015 15015015 GCTGGAGTGCAGTGGCACGATCTCGGCTCACTACAAGCTCTGCCTCCCAGGTTCACGCCATTCTC GCTGGAGTGCAGTGGCACGATCTCGGCTCACTGCAAGCTCTGCCTCCCAGGTTCACGCCATTCTC A G PDXDC1 Ensembl:ENSG00000179889 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1210123087 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_125777,RMVar_hsa_circ_176498,RMVar_hsa_circ_5646,RMVar_hsa_circ_69488,RMVar_hsa_circ_321402,RMVar_hsa_circ_346116,RMVar_hsa_circ_82502,RMVar_hsa_circ_39291,RMVar_hsa_circ_176503,RMVar_hsa_circ_176504 11589 RMVar_ID_11589 Human_SNP_ID_595686140 A-to-I Human chr16 + 15015015 15015015 15015015 GCTGGAGTGCAGTGGCACGATCTCGGCTCACTACAAGCTCTGCCTCCCAGGTTCACGCCATTCTC GCTGGAGTGCAGTGGCACGATCTCGGCTCACTTCAAGCTCTGCCTCCCAGGTTCACGCCATTCTC A T PDXDC1 Ensembl:ENSG00000179889 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1210123087 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_125777,RMVar_hsa_circ_176498,RMVar_hsa_circ_5646,RMVar_hsa_circ_69488,RMVar_hsa_circ_321402,RMVar_hsa_circ_346116,RMVar_hsa_circ_82502,RMVar_hsa_circ_39291,RMVar_hsa_circ_176503,RMVar_hsa_circ_176504 11590 RMVar_ID_11590 Human_SNP_ID_595686174 A-to-I Human chr16 + 15015077 15015077 15015077 CTCCCGCCTCGGCCCCGCGAGTACCTGGGACTATAGGCGCCCACCACTACACCCGGCTAATTTTG CTCCCGCCTCGGCCCCGCGAGTACCTGGGACTGTAGGCGCCCACCACTACACCCGGCTAATTTTG A G PDXDC1 Ensembl:ENSG00000179889 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs192812417 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_125777,RMVar_hsa_circ_176498,RMVar_hsa_circ_5646,RMVar_hsa_circ_69488,RMVar_hsa_circ_321402,RMVar_hsa_circ_346116,RMVar_hsa_circ_82502,RMVar_hsa_circ_39291,RMVar_hsa_circ_176503,RMVar_hsa_circ_176504 11591 RMVar_ID_11591 Human_SNP_ID_595686330 A-to-I Human chr16 + 15015596 15015596 15015596 AAAATTAGCCGGGCGTGGTGGCCACCGCCTGTAATCCCACCTACTTGGGAGGCTGAGGCAAGGAG AAAATTAGCCGGGCGTGGTGGCCACCGCCTGTGATCCCACCTACTTGGGAGGCTGAGGCAAGGAG A G PDXDC1 Ensembl:ENSG00000179889 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1291447199 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_125777,RMVar_hsa_circ_176498,RMVar_hsa_circ_5646,RMVar_hsa_circ_69488,RMVar_hsa_circ_321402,RMVar_hsa_circ_346116,RMVar_hsa_circ_82502,RMVar_hsa_circ_39291,RMVar_hsa_circ_176503,RMVar_hsa_circ_176504 11592 RMVar_ID_11592 Human_SNP_ID_595688981 A-to-I Human chr16 + 15023530 15023530 15023530 TAAATACAAAAAGTAGCCGCGCATGGTGGCACACGCCTGTAGTCCCAGCTACTGGGGAGGCTGAA TAAATACAAAAAGTAGCCGCGCATGGTGGCACCCGCCTGTAGTCCCAGCTACTGGGGAGGCTGAA A C PDXDC1 Ensembl:ENSG00000179889 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs888342601 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12672053,Human_RBP_ID_25192810 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_176507,RMVar_hsa_circ_370323 11593 RMVar_ID_11593 Human_SNP_ID_595688982 A-to-I Human chr16 + 15023530 15023530 15023530 TAAATACAAAAAGTAGCCGCGCATGGTGGCACACGCCTGTAGTCCCAGCTACTGGGGAGGCTGAA TAAATACAAAAAGTAGCCGCGCATGGTGGCACGCGCCTGTAGTCCCAGCTACTGGGGAGGCTGAA A G PDXDC1 Ensembl:ENSG00000179889 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs888342601 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12672053,Human_RBP_ID_25192810 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_176507,RMVar_hsa_circ_370323 11594 RMVar_ID_11594 Human_SNP_ID_595688983 A-to-I Human chr16 + 15023530 15023530 15023530 TAAATACAAAAAGTAGCCGCGCATGGTGGCACACGCCTGTAGTCCCAGCTACTGGGGAGGCTGAA TAAATACAAAAAGTAGCCGCGCATGGTGGCACTCGCCTGTAGTCCCAGCTACTGGGGAGGCTGAA A T PDXDC1 Ensembl:ENSG00000179889 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs888342601 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12672053,Human_RBP_ID_25192810 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_176507,RMVar_hsa_circ_370323 11595 RMVar_ID_11595 Human_SNP_ID_595689286 A-to-I Human chr16 - 15024467 15024467 15024467 AGGAGGCGGAGGTTAGAGTGAGCCAAGATCGCACCACTGCACTCCAGTCTGGGCTACATAGTGAG AGGAGGCGGAGGTTAGAGTGAGCCAAGATCGCCCCACTGCACTCCAGTCTGGGCTACATAGTGAG T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1445829560 Functional Loss SNV dbSNP153 33..33 33 - - - 11596 RMVar_ID_11596 Human_SNP_ID_595689297 A-to-I Human chr16 + 15024481 15024481 15024481 CAGACTGGAGTGCAGTGGTGCGATCTTGGCTCACTCTAACCTCCGCCTCCTGGGTCCCTGTTCAA CAGACTGGAGTGCAGTGGTGCGATCTTGGCTCTCTCTAACCTCCGCCTCCTGGGTCCCTGTTCAA A T PDXDC1 Ensembl:ENSG00000179889 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1356687534 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8428119 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_176507,RMVar_hsa_circ_370323 11597 RMVar_ID_11597 Human_SNP_ID_595689315 A-to-I Human chr16 - 15024541 15024541 15024541 GGACATGGTGGCATGCGCCTGTAACCCCAGCTACTCGGGAGGCTGAGGCAGGAGAACTGCTTGAA GGACATGGTGGCATGCGCCTGTAACCCCAGCTGCTCGGGAGGCTGAGGCAGGAGAACTGCTTGAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs555330379 Functional Loss SNV dbSNP153 33..33 33 - - - 11598 RMVar_ID_11598 Human_SNP_ID_595691528 A-to-I Human chr16 + 15030419 15030416 15030419 ATACAAAAAATTAGCCAGGCATGGTGGTACACACCTGCAGTCCCAGCTACTTGGGAGGCTGAGGC ATACAAAAAATTAGCCAGGCATGGTGGTAC___CCTGCAGTCCCAGCTACTTGGGAGGCTGAGGC CACA C PDXDC1 Ensembl:ENSG00000179889 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1247064464 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,RMVar_hsa_circ_39291 11599 RMVar_ID_11599 Human_SNP_ID_595698283 A-to-I Human chr16 - 15050522 15050522 15050522 TTCCTTGTTGCCCAGGCTGGTTTTGAACTCTTAGGCTCAAGCAGTCCTCCCTCCTCAGCCTCCCA TTCCTTGTTGCCCAGGCTGGTTTTGAACTCTTGGGCTCAAGCAGTCCTCCCTCCTCAGCCTCCCA T C NTAN1 Ensembl:ENSG00000157045 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1261639221 Functional Loss SNV dbSNP153 33..33 33 - - - 11600 RMVar_ID_11600 Human_SNP_ID_595701550 A-to-I Human chr16 - 15062149 15062149 15062149 CAGAGGGAGCTTTTGTTCTGTTCTGTTTTTCTAGAGACATGGTCTCGCTATGTTGCCCAGGCTGG CAGAGGGAGCTTTTGTTCTGTTCTGTTTTTCTCGAGACATGGTCTCGCTATGTTGCCCAGGCTGG T G RRN3 Ensembl:ENSG00000085721 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs531530834 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106090,RMVar_hsa_circ_176517 11601 RMVar_ID_11601 Human_SNP_ID_595720124 A-to-I Human chr16 - 15122158 15122155 15122159 GACTTTTTTGTTTGTTTGTTTGTTTTTTAGACAGAGTCTCACTCTGTCGCCCAGGCTGGAGTGCA GACTTTTTTGTTTGTTTGTTTGTTTTTTAGA____GTCTCACTCTGTCGCCCAGGCTGGAGTGCA CTCTG C AC139256.3,NPIPP1 Ensembl:ENSG00000270580,Ensembl:ENSG00000188599 lincRNA,Pseudogene intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041967532 Functional Loss DEL dbSNP153 32..35 33 - - - RMVar_hsa_circ_124864,RMVar_hsa_circ_176532 11602 RMVar_ID_11602 Human_SNP_ID_595780573 A-to-I Human chr16 - 15363876 15363876 15363876 GCGTCTGCTCTATCCCCTTCCACCCTCAGCGGATGATAATCTCAAGACACCTCCCGAGTGTCTGC GCGTCTGCTCTATCCCCTTCCACCCTCAGCGGTTGATAATCTCAAGACACCTCCCGAGTGTCTGC T A NPIPA5 Ensembl:ENSG00000183793 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs752982027 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22053940,Human_RBP_ID_22935931 11603 RMVar_ID_11603 Human_SNP_ID_595780574 A-to-I Human chr16 - 15363876 15363876 15363876 GCGTCTGCTCTATCCCCTTCCACCCTCAGCGGATGATAATCTCAAGACACCTCCCGAGTGTCTGC GCGTCTGCTCTATCCCCTTCCACCCTCAGCGGGTGATAATCTCAAGACACCTCCCGAGTGTCTGC T C NPIPA5 Ensembl:ENSG00000183793 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs752982027 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22053940,Human_RBP_ID_22935931 11604 RMVar_ID_11604 Human_SNP_ID_595780575 A-to-I Human chr16 - 15363876 15363876 15363876 GCGTCTGCTCTATCCCCTTCCACCCTCAGCGGATGATAATCTCAAGACACCTCCCGAGTGTCTGC GCGTCTGCTCTATCCCCTTCCACCCTCAGCGGCTGATAATCTCAAGACACCTCCCGAGTGTCTGC T G NPIPA5 Ensembl:ENSG00000183793 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs752982027 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22053940,Human_RBP_ID_22935931 11605 RMVar_ID_11605 Human_SNP_ID_595791883 A-to-I Human chr16 + 15404701 15404701 15404701 AAAATTAGCCAGGTATGGTGGTGAGTGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTAGCCAGGTATGGTGGTGAGTGCCTGTCATCCCAGCTACTCGGGAGGCTGAGGCAGGAGA A C MPV17L,AC140504.1 Ensembl:ENSG00000156968,Ensembl:ENSG00000261130 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1446410614 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_93945,RMVar_hsa_circ_84522,RMVar_hsa_circ_176538,RMVar_hsa_circ_176539 11606 RMVar_ID_11606 Human_SNP_ID_595792916 A-to-I Human chr16 + 15408742 15408742 15408742 CTCCTGCCTCAGGCTCCTGAGTAGCTGGGATTACAGGCACGTGACACCAGGCCCAGCTGATTTTT CTCCTGCCTCAGGCTCCTGAGTAGCTGGGATTTCAGGCACGTGACACCAGGCCCAGCTGATTTTT A T MPV17L,AC140504.1 Ensembl:ENSG00000156968,Ensembl:ENSG00000261130 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs564932375 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_103195,RMVar_hsa_circ_93945,RMVar_hsa_circ_84522,RMVar_hsa_circ_176538,RMVar_hsa_circ_176539,RMVar_hsa_circ_176540 11607 RMVar_ID_11607 Human_SNP_ID_595792927 A-to-I Human chr16 + 15408808 15408807 15408809 TATTTTTGTTCATTTGCTTTTGTTTTTGACACAGAGTCTCGCTCTGTCGCCCAGGCTGGAATGCA TATTTTTGTTCATTTGCTTTTGTTTTTGACAC__AGTCTCGCTCTGTCGCCCAGGCTGGAATGCA CAG C MPV17L,AC140504.1 Ensembl:ENSG00000156968,Ensembl:ENSG00000261130 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1362457233 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_103195,RMVar_hsa_circ_93945,RMVar_hsa_circ_84522,RMVar_hsa_circ_176538,RMVar_hsa_circ_176539,RMVar_hsa_circ_176540 11608 RMVar_ID_11608 Human_SNP_ID_595792928 A-to-I Human chr16 + 15408808 15408808 15408808 TATTTTTGTTCATTTGCTTTTGTTTTTGACACAGAGTCTCGCTCTGTCGCCCAGGCTGGAATGCA TATTTTTGTTCATTTGCTTTTGTTTTTGACACGGAGTCTCGCTCTGTCGCCCAGGCTGGAATGCA A G MPV17L,AC140504.1 Ensembl:ENSG00000156968,Ensembl:ENSG00000261130 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1292717426 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_103195,RMVar_hsa_circ_93945,RMVar_hsa_circ_84522,RMVar_hsa_circ_176538,RMVar_hsa_circ_176539,RMVar_hsa_circ_176540 11609 RMVar_ID_11609 Human_SNP_ID_595792940 A-to-I Human chr16 + 15408835 15408835 15408835 GACACAGAGTCTCGCTCTGTCGCCCAGGCTGGAATGCAGTTGTGAGATCTCGGCTCACTGCAAGC GACACAGAGTCTCGCTCTGTCGCCCAGGCTGGGATGCAGTTGTGAGATCTCGGCTCACTGCAAGC A G MPV17L,AC140504.1 Ensembl:ENSG00000156968,Ensembl:ENSG00000261130 Protein coding,Protein coding 3'UTR,intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs377549401 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_103195,RMVar_hsa_circ_93945,RMVar_hsa_circ_84522,RMVar_hsa_circ_176538,RMVar_hsa_circ_176539,RMVar_hsa_circ_176540 11610 RMVar_ID_11610 Human_SNP_ID_595792996 A-to-I Human chr16 + 15408966 15408966 15408966 ACGATGCCTAGCTAATTTTTTGTATTTTTAGTAGAGATGAAGTTTCACCGTGTTGGCCAGGATGG ACGATGCCTAGCTAATTTTTTGTATTTTTAGTGGAGATGAAGTTTCACCGTGTTGGCCAGGATGG A G MPV17L,AC140504.1 Ensembl:ENSG00000156968,Ensembl:ENSG00000261130 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1468006733 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12672973 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_103195,RMVar_hsa_circ_93945,RMVar_hsa_circ_84522,RMVar_hsa_circ_176538,RMVar_hsa_circ_176539,RMVar_hsa_circ_176540 11611 RMVar_ID_11611 Human_SNP_ID_595793017 A-to-I Human chr16 + 15409024 15409024 15409024 AGGATGGTCTTGATCTCCTGACCGCATAATCCACCCACCTCGGCCTCCCAAAGTGCTGGGATTAC AGGATGGTCTTGATCTCCTGACCGCATAATCCCCCCACCTCGGCCTCCCAAAGTGCTGGGATTAC A C MPV17L,AC140504.1 Ensembl:ENSG00000156968,Ensembl:ENSG00000261130 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1356585987 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_103195,RMVar_hsa_circ_93945,RMVar_hsa_circ_84522,RMVar_hsa_circ_176538,RMVar_hsa_circ_176539,RMVar_hsa_circ_176540 11612 RMVar_ID_11612 Human_SNP_ID_595793306 A-to-I Human chr16 + 15410196 15410196 15410196 AGTTTCACTTGGACGTAGTGGTTCACGCTTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGAGG AGTTTCACTTGGACGTAGTGGTTCACGCTTGTCATCCCAGCACTTTGGGAGGCTGAGGTGGGAGG A C MPV17L,AC140504.1 Ensembl:ENSG00000156968,Ensembl:ENSG00000261130 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs113378073 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 11613 RMVar_ID_11613 Human_SNP_ID_595793389 A-to-I Human chr16 + 15410483 15410483 15410483 TGAGGCAGACGAATGGCATGAACCCGGGAGGCAGAGATTGCAGTGAGCTGAGATTGTGCCACTGC TGAGGCAGACGAATGGCATGAACCCGGGAGGCGGAGATTGCAGTGAGCTGAGATTGTGCCACTGC A G MPV17L,AC140504.1 Ensembl:ENSG00000156968,Ensembl:ENSG00000261130 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs975659573 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 11614 RMVar_ID_11614 Human_SNP_ID_595793556 A-to-I Human chr16 + 15411207 15411202 15411208 TGAGCAGAGATCAGGCCACTGCACTCCAGCCTAGGCGACAGAGCGAGAATCTGTCTCAAAACAAA TGAGCAGAGATCAGGCCACTGCACTCCA______GCGACAGAGCGAGAATCTGTCTCAAAACAAA AGCCTAG A MPV17L,AC140504.1 Ensembl:ENSG00000156968,Ensembl:ENSG00000261130 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1447241389 Functional Loss DEL dbSNP153 29..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 11615 RMVar_ID_11615 Human_SNP_ID_595793857 A-to-I Human chr16 + 15412385 15412385 15412385 CCAGGAGGTGGAGGTTGCAGTGAGCCGAGATCACGCCACTGCACTCCAGGAAGGGCAACAGAGCA CCAGGAGGTGGAGGTTGCAGTGAGCCGAGATCGCGCCACTGCACTCCAGGAAGGGCAACAGAGCA A G MPV17L,AC140504.1 Ensembl:ENSG00000156968,Ensembl:ENSG00000261130 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170538162 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 11616 RMVar_ID_11616 Human_SNP_ID_595850401 A-to-I Human chr16 - 15614671 15614671 15614671 CCCCTGCCTCAGTCTCCTGAGGAGCTGGGACTACAGGCGCCCGCCACCACGCCCGGCTAATTTTT CCCCTGCCTCAGTCTCCTGAGGAGCTGGGACTGCAGGCGCCCGCCACCACGCCCGGCTAATTTTT T C MARF1 Ensembl:ENSG00000166783 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1341024399 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55172,RMVar_hsa_circ_125353,RMVar_hsa_circ_176550,RMVar_hsa_circ_176551,RMVar_hsa_circ_347986,RMVar_hsa_circ_368573,RMVar_hsa_circ_298197 11617 RMVar_ID_11617 Human_SNP_ID_595861142 A-to-I Human chr16 + 15652102 15652102 15652102 GCTAATTCTTAGTAGAGATGGGGTTTCACCATATTGGCCAGGCTGGTCTCAAACTTCTGACCTCG GCTAATTCTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTTCTGACCTCG A G NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs920555214 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_102745,RMVar_hsa_circ_86644,RMVar_hsa_circ_176565,RMVar_hsa_circ_176566 11618 RMVar_ID_11618 Human_SNP_ID_595861143 A-to-I Human chr16 + 15652102 15652102 15652102 GCTAATTCTTAGTAGAGATGGGGTTTCACCATATTGGCCAGGCTGGTCTCAAACTTCTGACCTCG GCTAATTCTTAGTAGAGATGGGGTTTCACCATTTTGGCCAGGCTGGTCTCAAACTTCTGACCTCG A T NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs920555214 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_102745,RMVar_hsa_circ_86644,RMVar_hsa_circ_176565,RMVar_hsa_circ_176566 11619 RMVar_ID_11619 Human_SNP_ID_595861799 A-to-I Human chr16 + 15654507 15654507 15654507 CCTGTAATCCGAGGTACTAGGGACGCTGAGGTAGGAGAATCGCTTGAAGCTGCGAGGCAGAGGTT CCTGTAATCCGAGGTACTAGGGACGCTGAGGTGGGAGAATCGCTTGAAGCTGCGAGGCAGAGGTT A G NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1212600795 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_102745,RMVar_hsa_circ_86644,RMVar_hsa_circ_176565,RMVar_hsa_circ_176566 11620 RMVar_ID_11620 Human_SNP_ID_595861968 A-to-I Human chr16 + 15655042 15655042 15655042 TTCATGTTGTTTATTTATTTATTTTTTGAGACAGAGTCTTGCTCTTGTGCCCAGGCTGGAGTGCA TTCATGTTGTTTATTTATTTATTTTTTGAGACGGAGTCTTGCTCTTGTGCCCAGGCTGGAGTGCA A G NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs574628756 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12868690 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_102745,RMVar_hsa_circ_86644,RMVar_hsa_circ_176565,RMVar_hsa_circ_176566 11621 RMVar_ID_11621 Human_SNP_ID_595862009 A-to-I Human chr16 + 15655207 15655206 15655208 ACCTGGCTAATTTTTGTGTTTCTAGTAGAGACAGGGTTTCACCATGTTGCCCAGGCTGGTCTTGA ACCTGGCTAATTTTTGTGTTTCTAGTAGAGAC__GGTTTCACCATGTTGCCCAGGCTGGTCTTGA CAG C NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1037032477 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_102745,RMVar_hsa_circ_86644,RMVar_hsa_circ_176565,RMVar_hsa_circ_176566 11622 RMVar_ID_11622 Human_SNP_ID_595862041 A-to-I Human chr16 + 15655365 15655365 15655365 AGTAGAGACGGGGTTCACCTTGTGCTGGTCTCAAACTCCTGGGCTCAAGCAATCTGCCCACCTCA AGTAGAGACGGGGTTCACCTTGTGCTGGTCTCGAACTCCTGGGCTCAAGCAATCTGCCCACCTCA A G NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs147265681 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_102745,RMVar_hsa_circ_86644,RMVar_hsa_circ_176565,RMVar_hsa_circ_176566 11623 RMVar_ID_11623 Human_SNP_ID_595862049 A-to-I Human chr16 + 15655397 15655397 15655397 AAACTCCTGGGCTCAAGCAATCTGCCCACCTCAGTCTGCCAAAGTGCTGGGATTACAGGCGTGAG AAACTCCTGGGCTCAAGCAATCTGCCCACCTCCGTCTGCCAAAGTGCTGGGATTACAGGCGTGAG A C NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1433515363 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_102745,RMVar_hsa_circ_86644,RMVar_hsa_circ_176565,RMVar_hsa_circ_176566 11624 RMVar_ID_11624 Human_SNP_ID_595863292 A-to-I Human chr16 + 15659888 15659888 15659888 CTCCTGCCTTAGCCGCCTGAGTAGCTGGGACTACAGGTACCTGCCACTGCGCCCGCCTAATTTTT CTCCTGCCTTAGCCGCCTGAGTAGCTGGGACTGCAGGTACCTGCCACTGCGCCCGCCTAATTTTT A G NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs928704210 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_102745,RMVar_hsa_circ_86644,RMVar_hsa_circ_176565,RMVar_hsa_circ_176566 11625 RMVar_ID_11625 Human_SNP_ID_595864861 A-to-I Human chr16 + 15665561 15665561 15665561 CCACCTCTGGGTTGAAGCAATTCTCGTGCCTCAGCTTCTCGAGTAGCTGGAATTACAGGCACCCA CCACCTCTGGGTTGAAGCAATTCTCGTGCCTCCGCTTCTCGAGTAGCTGGAATTACAGGCACCCA A C NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1338960609 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_20321,RMVar_hsa_circ_304453,RMVar_hsa_circ_102745,RMVar_hsa_circ_86644,RMVar_hsa_circ_176565,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_176570,RMVar_hsa_circ_176568 11626 RMVar_ID_11626 Human_SNP_ID_595864952 A-to-I Human chr16 + 15665890 15665890 15665890 TCGATTCTCTTGCCTCAGCCTCCCGAGTAGCTAGGATTACAGGCATGCACCACCATGCCCAGCTA TCGATTCTCTTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCATGCACCACCATGCCCAGCTA A G NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1483530391 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_20321,RMVar_hsa_circ_304453,RMVar_hsa_circ_102745,RMVar_hsa_circ_86644,RMVar_hsa_circ_176565,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_176570,RMVar_hsa_circ_176568 11627 RMVar_ID_11627 Human_SNP_ID_595865646 A-to-I Human chr16 + 15668018 15668018 15668018 ACAGGGTCTTGCTCTGTTGCCCAGACTGGAGTACAGTGGCTGGATTACAGCTCACTGCACCCTGG ACAGGGTCTTGCTCTGTTGCCCAGACTGGAGTGCAGTGGCTGGATTACAGCTCACTGCACCCTGG A G NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs991124807 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_20321,RMVar_hsa_circ_102745,RMVar_hsa_circ_86644,RMVar_hsa_circ_176565,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_176570,RMVar_hsa_circ_176568,RMVar_hsa_circ_3008,RMVar_hsa_circ_34873 11628 RMVar_ID_11628 Human_SNP_ID_595865673 A-to-I Human chr16 + 15668108 15668108 15668108 CACCTGGGCCGGGCGAGGTGGTGCATACCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGCAG CACCTGGGCCGGGCGAGGTGGTGCATACCTGTGATCCCAGCACTTTGGGAGGCTGAGGTGGGCAG A G NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1221483899 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_20321,RMVar_hsa_circ_102745,RMVar_hsa_circ_86644,RMVar_hsa_circ_176565,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_176570,RMVar_hsa_circ_176568,RMVar_hsa_circ_3008,RMVar_hsa_circ_34873 11629 RMVar_ID_11629 Human_SNP_ID_595865752 A-to-I Human chr16 + 15668454 15668454 15668454 GCCTGGTTAGTTTTTGTATTTTTTATAGAGACAGGGTTTCGCTGTGTTGCCCAGGCTGGTCTTGA GCCTGGTTAGTTTTTGTATTTTTTATAGAGACGGGGTTTCGCTGTGTTGCCCAGGCTGGTCTTGA A G NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1251623338 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_20321,RMVar_hsa_circ_102745,RMVar_hsa_circ_86644,RMVar_hsa_circ_176565,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_176570,RMVar_hsa_circ_176568,RMVar_hsa_circ_3008,RMVar_hsa_circ_34873 11630 RMVar_ID_11630 Human_SNP_ID_595866330 A-to-I Human chr16 + 15670416 15670416 15670416 GCGGTGGCTCATGCCTGTTATCCCAGCACTTCAGGAGGCCGAGGTGGGCAGATCACCTGAGGTTG GCGGTGGCTCATGCCTGTTATCCCAGCACTTCGGGAGGCCGAGGTGGGCAGATCACCTGAGGTTG A G NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs910537681 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_20321,RMVar_hsa_circ_102745,RMVar_hsa_circ_86644,RMVar_hsa_circ_176565,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_176570,RMVar_hsa_circ_176568,RMVar_hsa_circ_3008,RMVar_hsa_circ_34873 11631 RMVar_ID_11631 Human_SNP_ID_595866338 A-to-I Human chr16 + 15670433 15670429 15670433 TTATCCCAGCACTTCAGGAGGCCGAGGTGGGCAGATCACCTGAGGTTGGGAGTTTGAGACCAGCC TTATCCCAGCACTTCAGGAGGCCGAGGTG____GATCACCTGAGGTTGGGAGTTTGAGACCAGCC GGGCA G NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1461130634 Functional Loss DEL dbSNP153 30..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_20321,RMVar_hsa_circ_102745,RMVar_hsa_circ_86644,RMVar_hsa_circ_176565,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_176570,RMVar_hsa_circ_176568,RMVar_hsa_circ_3008,RMVar_hsa_circ_34873 11632 RMVar_ID_11632 Human_SNP_ID_595866723 A-to-I Human chr16 + 15671803 15671803 15671803 ACCTCTGACTTCCAGGCTTAAGTGATCCTCCCACCTCAGCCTCCCAAGTAGCTGAGATTACAGGC ACCTCTGACTTCCAGGCTTAAGTGATCCTCCCCCCTCAGCCTCCCAAGTAGCTGAGATTACAGGC A C NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1057343871 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_20321,RMVar_hsa_circ_102745,RMVar_hsa_circ_86644,RMVar_hsa_circ_176565,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_176570,RMVar_hsa_circ_176568,RMVar_hsa_circ_3008,RMVar_hsa_circ_34873 11633 RMVar_ID_11633 Human_SNP_ID_595866724 A-to-I Human chr16 + 15671803 15671803 15671803 ACCTCTGACTTCCAGGCTTAAGTGATCCTCCCACCTCAGCCTCCCAAGTAGCTGAGATTACAGGC ACCTCTGACTTCCAGGCTTAAGTGATCCTCCCGCCTCAGCCTCCCAAGTAGCTGAGATTACAGGC A G NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1057343871 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_20321,RMVar_hsa_circ_102745,RMVar_hsa_circ_86644,RMVar_hsa_circ_176565,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_176570,RMVar_hsa_circ_176568,RMVar_hsa_circ_3008,RMVar_hsa_circ_34873 11634 RMVar_ID_11634 Human_SNP_ID_595866866 A-to-I Human chr16 + 15672268 15672268 15672268 TGTCCTCGCTAACATGGTGAAACCCCGTCTCTACTAAAAATAAAAAAATTAGCTGGGCATGGTGG TGTCCTCGCTAACATGGTGAAACCCCGTCTCTGCTAAAAATAAAAAAATTAGCTGGGCATGGTGG A G NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1376300851 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_20321,RMVar_hsa_circ_102745,RMVar_hsa_circ_86644,RMVar_hsa_circ_176565,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_176570,RMVar_hsa_circ_176568,RMVar_hsa_circ_3008,RMVar_hsa_circ_34873 11635 RMVar_ID_11635 Human_SNP_ID_595870206 A-to-I Human chr16 + 15682748 15682747 15682749 TTCATTTTATTTTATTTATTTATTTTTGAGACAGAGTCTTGCTCTGTAGCCCAGGCTGGAGTGCA TTCATTTTATTTTATTTATTTATTTTTGAGAC__AGTCTTGCTCTGTAGCCCAGGCTGGAGTGCA CAG C NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1470493615 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_24751,RMVar_hsa_circ_20321,RMVar_hsa_circ_86644,RMVar_hsa_circ_176565,RMVar_hsa_circ_96422,RMVar_hsa_circ_98515,RMVar_hsa_circ_24708,RMVar_hsa_circ_176567,RMVar_hsa_circ_176569,RMVar_hsa_circ_176568,RMVar_hsa_circ_3008,RMVar_hsa_circ_105546,RMVar_hsa_circ_110234,RMVar_hsa_circ_176576,RMVar_hsa_circ_176577,RMVar_hsa_circ_176575 11636 RMVar_ID_11636 Human_SNP_ID_595870562 A-to-I Human chr16 + 15684100 15684100 15684100 TAAAAATGCAAAAATTAGCCAGGCATGGTGGCAGGCGCCTGTAATCCCAGTTACTTGACAGACTG TAAAAATGCAAAAATTAGCCAGGCATGGTGGCTGGCGCCTGTAATCCCAGTTACTTGACAGACTG A T NDE1,AC026401.2 Ensembl:ENSG00000072864,Ensembl:ENSG00000262380 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1379393097 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_24751,RMVar_hsa_circ_20321,RMVar_hsa_circ_86644,RMVar_hsa_circ_176565,RMVar_hsa_circ_96422,RMVar_hsa_circ_98515,RMVar_hsa_circ_24708,RMVar_hsa_circ_176567,RMVar_hsa_circ_176569,RMVar_hsa_circ_176568,RMVar_hsa_circ_3008,RMVar_hsa_circ_105546,RMVar_hsa_circ_110234,RMVar_hsa_circ_176576,RMVar_hsa_circ_176577,RMVar_hsa_circ_176575 11637 RMVar_ID_11637 Human_SNP_ID_595870676 A-to-I Human chr16 + 15684482 15684482 15684482 GGATGTGGTGGTGCGTGCCTGTAATCCCAGCTACTTGGGAGGCTGAGACAGAAGAATCATTTGAA GGATGTGGTGGTGCGTGCCTGTAATCCCAGCTGCTTGGGAGGCTGAGACAGAAGAATCATTTGAA A G NDE1,AC026401.2 Ensembl:ENSG00000072864,Ensembl:ENSG00000262380 Protein coding,lincRNA intron,exon GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1308524249 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_24751,RMVar_hsa_circ_20321,RMVar_hsa_circ_86644,RMVar_hsa_circ_176565,RMVar_hsa_circ_96422,RMVar_hsa_circ_98515,RMVar_hsa_circ_24708,RMVar_hsa_circ_176567,RMVar_hsa_circ_176569,RMVar_hsa_circ_176568,RMVar_hsa_circ_3008,RMVar_hsa_circ_105546,RMVar_hsa_circ_110234,RMVar_hsa_circ_176576,RMVar_hsa_circ_176577,RMVar_hsa_circ_176575 11638 RMVar_ID_11638 Human_SNP_ID_595870967 A-to-I Human chr16 + 15685453 15685453 15685453 TTTTACTTTTTGTAGAGACAGGGTCTCTCTATATTACCCAGGCTGGTCTTGAACCCTGGGCCTCA TTTTACTTTTTGTAGAGACAGGGTCTCTCTATGTTACCCAGGCTGGTCTTGAACCCTGGGCCTCA A G NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1346598840 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_24751,RMVar_hsa_circ_20321,RMVar_hsa_circ_86644,RMVar_hsa_circ_176565,RMVar_hsa_circ_96422,RMVar_hsa_circ_98515,RMVar_hsa_circ_24708,RMVar_hsa_circ_176567,RMVar_hsa_circ_176569,RMVar_hsa_circ_176568,RMVar_hsa_circ_3008,RMVar_hsa_circ_105546,RMVar_hsa_circ_110234,RMVar_hsa_circ_176576,RMVar_hsa_circ_176577,RMVar_hsa_circ_176575 11639 RMVar_ID_11639 Human_SNP_ID_595871332 A-to-I Human chr16 + 15686768 15686768 15686768 TCACTTTGTTGTCTAGGCTGGAGTGCAGTGGTATAATCTGGGCTCACTACAACCTCTGCTTCCTG TCACTTTGTTGTCTAGGCTGGAGTGCAGTGGTGTAATCTGGGCTCACTACAACCTCTGCTTCCTG A G NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs545743207 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17563991 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_24751,RMVar_hsa_circ_20321,RMVar_hsa_circ_86644,RMVar_hsa_circ_176565,RMVar_hsa_circ_96422,RMVar_hsa_circ_98515,RMVar_hsa_circ_24708,RMVar_hsa_circ_176567,RMVar_hsa_circ_176569,RMVar_hsa_circ_176568,RMVar_hsa_circ_3008,RMVar_hsa_circ_105546,RMVar_hsa_circ_110234,RMVar_hsa_circ_176578,RMVar_hsa_circ_176576,RMVar_hsa_circ_176577,RMVar_hsa_circ_176575,RMVar_hsa_circ_111356 11640 RMVar_ID_11640 Human_SNP_ID_595871333 A-to-I Human chr16 + 15686770 15686770 15686770 ACTTTGTTGTCTAGGCTGGAGTGCAGTGGTATAATCTGGGCTCACTACAACCTCTGCTTCCTGGC ACTTTGTTGTCTAGGCTGGAGTGCAGTGGTATTATCTGGGCTCACTACAACCTCTGCTTCCTGGC A T NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs964011862 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17563991 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_24751,RMVar_hsa_circ_20321,RMVar_hsa_circ_86644,RMVar_hsa_circ_176565,RMVar_hsa_circ_96422,RMVar_hsa_circ_98515,RMVar_hsa_circ_24708,RMVar_hsa_circ_176567,RMVar_hsa_circ_176569,RMVar_hsa_circ_176568,RMVar_hsa_circ_3008,RMVar_hsa_circ_105546,RMVar_hsa_circ_110234,RMVar_hsa_circ_176578,RMVar_hsa_circ_176576,RMVar_hsa_circ_176577,RMVar_hsa_circ_176575,RMVar_hsa_circ_111356 11641 RMVar_ID_11641 Human_SNP_ID_595871340 A-to-I Human chr16 + 15686784 15686784 15686784 GCTGGAGTGCAGTGGTATAATCTGGGCTCACTACAACCTCTGCTTCCTGGCAGTTCTCCCACCTC GCTGGAGTGCAGTGGTATAATCTGGGCTCACTGCAACCTCTGCTTCCTGGCAGTTCTCCCACCTC A G NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1016796721 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17563991 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_24751,RMVar_hsa_circ_20321,RMVar_hsa_circ_86644,RMVar_hsa_circ_176565,RMVar_hsa_circ_96422,RMVar_hsa_circ_98515,RMVar_hsa_circ_24708,RMVar_hsa_circ_176567,RMVar_hsa_circ_176569,RMVar_hsa_circ_176568,RMVar_hsa_circ_3008,RMVar_hsa_circ_105546,RMVar_hsa_circ_110234,RMVar_hsa_circ_176578,RMVar_hsa_circ_176576,RMVar_hsa_circ_176577,RMVar_hsa_circ_176575,RMVar_hsa_circ_111356 11642 RMVar_ID_11642 Human_SNP_ID_595872023 A-to-I Human chr16 + 15688898 15688898 15688898 TTTTATATTTTTAATAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGACCC TTTTATATTTTTAATAGAGATGGGGTTTCACCGTGTTGGCCAGGCTGGTCTTGAACTCCTGACCC A G NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1467772514 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_20321,RMVar_hsa_circ_86644,RMVar_hsa_circ_176565,RMVar_hsa_circ_96422,RMVar_hsa_circ_98515,RMVar_hsa_circ_176567,RMVar_hsa_circ_176568,RMVar_hsa_circ_3008,RMVar_hsa_circ_105546,RMVar_hsa_circ_110234,RMVar_hsa_circ_176578,RMVar_hsa_circ_176576,RMVar_hsa_circ_176577,RMVar_hsa_circ_111356,RMVar_hsa_circ_176579,RMVar_hsa_circ_354216 11643 RMVar_ID_11643 Human_SNP_ID_595872155 A-to-I Human chr16 + 15689431 15689429 15689431 GGAGGATGACTTGAGCCCAGGAGTTCAAGGTTACATTGAGCTATGATTGTGCCACCGCACCCCAG GGAGGATGACTTGAGCCCAGGAGTTCAAGGT__CATTGAGCTATGATTGTGCCACCGCACCCCAG TTA T NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1444596956 Functional Loss DEL dbSNP153 32..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_20321,RMVar_hsa_circ_86644,RMVar_hsa_circ_176565,RMVar_hsa_circ_96422,RMVar_hsa_circ_98515,RMVar_hsa_circ_176567,RMVar_hsa_circ_176568,RMVar_hsa_circ_3008,RMVar_hsa_circ_105546,RMVar_hsa_circ_110234,RMVar_hsa_circ_176578,RMVar_hsa_circ_176576,RMVar_hsa_circ_176577,RMVar_hsa_circ_111356,RMVar_hsa_circ_176579,RMVar_hsa_circ_354216 11644 RMVar_ID_11644 Human_SNP_ID_595872160 A-to-I Human chr16 + 15689441 15689441 15689441 TTGAGCCCAGGAGTTCAAGGTTACATTGAGCTATGATTGTGCCACCGCACCCCAGCCTGGGTGAC TTGAGCCCAGGAGTTCAAGGTTACATTGAGCTGTGATTGTGCCACCGCACCCCAGCCTGGGTGAC A G NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1375153726 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_20321,RMVar_hsa_circ_86644,RMVar_hsa_circ_176565,RMVar_hsa_circ_96422,RMVar_hsa_circ_98515,RMVar_hsa_circ_176567,RMVar_hsa_circ_176568,RMVar_hsa_circ_3008,RMVar_hsa_circ_105546,RMVar_hsa_circ_110234,RMVar_hsa_circ_176578,RMVar_hsa_circ_176576,RMVar_hsa_circ_176577,RMVar_hsa_circ_111356,RMVar_hsa_circ_176579,RMVar_hsa_circ_354216 11645 RMVar_ID_11645 Human_SNP_ID_595872261 A-to-I Human chr16 + 15689829 15689829 15689829 AGGTGTGGTGGTGCGTGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCACTTGAA AGGTGTGGTGGTGCGTGCCTGTAATCCCAGCTGCTTGGGAGGCTGAGGCAGGAGAATCACTTGAA A G NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1457564301 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_20321,RMVar_hsa_circ_86644,RMVar_hsa_circ_176565,RMVar_hsa_circ_96422,RMVar_hsa_circ_98515,RMVar_hsa_circ_176567,RMVar_hsa_circ_176568,RMVar_hsa_circ_3008,RMVar_hsa_circ_105546,RMVar_hsa_circ_110234,RMVar_hsa_circ_176578,RMVar_hsa_circ_176576,RMVar_hsa_circ_176577,RMVar_hsa_circ_111356,RMVar_hsa_circ_176579,RMVar_hsa_circ_354216 11646 RMVar_ID_11646 Human_SNP_ID_595872392 A-to-I Human chr16 + 15690184 15690184 15690184 GTCTTGCCTCAGCCTCCCAAGCAGCTGGGACTACAGGCGCTCACCACCACGCATGGCTAATTTTT GTCTTGCCTCAGCCTCCCAAGCAGCTGGGACTGCAGGCGCTCACCACCACGCATGGCTAATTTTT A G NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1443987443 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_20321,RMVar_hsa_circ_86644,RMVar_hsa_circ_176565,RMVar_hsa_circ_96422,RMVar_hsa_circ_98515,RMVar_hsa_circ_176567,RMVar_hsa_circ_176568,RMVar_hsa_circ_3008,RMVar_hsa_circ_105546,RMVar_hsa_circ_110234,RMVar_hsa_circ_176578,RMVar_hsa_circ_176576,RMVar_hsa_circ_176577,RMVar_hsa_circ_111356,RMVar_hsa_circ_176579,RMVar_hsa_circ_354216 11647 RMVar_ID_11647 Human_SNP_ID_595872402 A-to-I Human chr16 + 15690210 15690210 15690210 GGGACTACAGGCGCTCACCACCACGCATGGCTAATTTTTTGTATTTTTAATAGAGACGGGGTTTT GGGACTACAGGCGCTCACCACCACGCATGGCTGATTTTTTGTATTTTTAATAGAGACGGGGTTTT A G NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1449671531 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_20321,RMVar_hsa_circ_86644,RMVar_hsa_circ_176565,RMVar_hsa_circ_96422,RMVar_hsa_circ_98515,RMVar_hsa_circ_176567,RMVar_hsa_circ_176568,RMVar_hsa_circ_3008,RMVar_hsa_circ_105546,RMVar_hsa_circ_110234,RMVar_hsa_circ_176578,RMVar_hsa_circ_176576,RMVar_hsa_circ_176577,RMVar_hsa_circ_111356,RMVar_hsa_circ_176579,RMVar_hsa_circ_354216 11648 RMVar_ID_11648 Human_SNP_ID_595872407 A-to-I Human chr16 + 15690226 15690226 15690226 ACCACCACGCATGGCTAATTTTTTGTATTTTTAATAGAGACGGGGTTTTGCCATGTTGGCCTGAA ACCACCACGCATGGCTAATTTTTTGTATTTTTGATAGAGACGGGGTTTTGCCATGTTGGCCTGAA A G NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1252170341 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_20321,RMVar_hsa_circ_86644,RMVar_hsa_circ_176565,RMVar_hsa_circ_96422,RMVar_hsa_circ_98515,RMVar_hsa_circ_176567,RMVar_hsa_circ_176568,RMVar_hsa_circ_3008,RMVar_hsa_circ_105546,RMVar_hsa_circ_110234,RMVar_hsa_circ_176578,RMVar_hsa_circ_176576,RMVar_hsa_circ_176577,RMVar_hsa_circ_111356,RMVar_hsa_circ_176579,RMVar_hsa_circ_354216 11649 RMVar_ID_11649 Human_SNP_ID_595872408 A-to-I Human chr16 + 15690229 15690229 15690229 ACCACGCATGGCTAATTTTTTGTATTTTTAATAGAGACGGGGTTTTGCCATGTTGGCCTGAAAAT ACCACGCATGGCTAATTTTTTGTATTTTTAATGGAGACGGGGTTTTGCCATGTTGGCCTGAAAAT A G NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1457344985 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_20321,RMVar_hsa_circ_86644,RMVar_hsa_circ_176565,RMVar_hsa_circ_96422,RMVar_hsa_circ_98515,RMVar_hsa_circ_176567,RMVar_hsa_circ_176568,RMVar_hsa_circ_3008,RMVar_hsa_circ_105546,RMVar_hsa_circ_110234,RMVar_hsa_circ_176578,RMVar_hsa_circ_176576,RMVar_hsa_circ_176577,RMVar_hsa_circ_111356,RMVar_hsa_circ_176579,RMVar_hsa_circ_354216 11650 RMVar_ID_11650 Human_SNP_ID_595873849 A-to-I Human chr16 + 15694369 15694369 15694369 CCTCTCTTCTTTTTTTCTTTTTTTTTAGAGACAGGGTCTTGCTCTGTTGCTCAGGCTGGAGTGTA CCTCTCTTCTTTTTTTCTTTTTTTTTAGAGACCGGGTCTTGCTCTGTTGCTCAGGCTGGAGTGTA A C NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs114119135 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,RMVar_hsa_circ_96422,RMVar_hsa_circ_176567,RMVar_hsa_circ_3008,RMVar_hsa_circ_110234,RMVar_hsa_circ_176578,RMVar_hsa_circ_176577,RMVar_hsa_circ_111356,RMVar_hsa_circ_176580,RMVar_hsa_circ_176579,RMVar_hsa_circ_354216,RMVar_hsa_circ_359592,RMVar_hsa_circ_176581,RMVar_hsa_circ_306571 11651 RMVar_ID_11651 Human_SNP_ID_595874033 A-to-I Human chr16 + 15694910 15694910 15694910 GAAACTGCCTTCTCTTTTGGCCGGGTGCTCATACCTGTAATCCCAGTGCTTTGGGAGGCCAAGGT GAAACTGCCTTCTCTTTTGGCCGGGTGCTCATGCCTGTAATCCCAGTGCTTTGGGAGGCCAAGGT A G NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs374398960 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17563992 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,RMVar_hsa_circ_96422,RMVar_hsa_circ_176567,RMVar_hsa_circ_3008,RMVar_hsa_circ_110234,RMVar_hsa_circ_176578,RMVar_hsa_circ_176577,RMVar_hsa_circ_111356,RMVar_hsa_circ_176580,RMVar_hsa_circ_176579,RMVar_hsa_circ_354216,RMVar_hsa_circ_359592,RMVar_hsa_circ_176581,RMVar_hsa_circ_306571 11652 RMVar_ID_11652 Human_SNP_ID_595874034 A-to-I Human chr16 + 15694910 15694910 15694910 GAAACTGCCTTCTCTTTTGGCCGGGTGCTCATACCTGTAATCCCAGTGCTTTGGGAGGCCAAGGT GAAACTGCCTTCTCTTTTGGCCGGGTGCTCATTCCTGTAATCCCAGTGCTTTGGGAGGCCAAGGT A T NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs374398960 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17563992 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,RMVar_hsa_circ_96422,RMVar_hsa_circ_176567,RMVar_hsa_circ_3008,RMVar_hsa_circ_110234,RMVar_hsa_circ_176578,RMVar_hsa_circ_176577,RMVar_hsa_circ_111356,RMVar_hsa_circ_176580,RMVar_hsa_circ_176579,RMVar_hsa_circ_354216,RMVar_hsa_circ_359592,RMVar_hsa_circ_176581,RMVar_hsa_circ_306571 11653 RMVar_ID_11653 Human_SNP_ID_595874796 A-to-I Human chr16 + 15697080 15697080 15697080 AGAGAGGGTCTTGTTTTGTGAGACAGGGTCTCACTCTGTCACCTAGGCTAGAATACGATGGCAGG AGAGAGGGTCTTGTTTTGTGAGACAGGGTCTCGCTCTGTCACCTAGGCTAGAATACGATGGCAGG A G NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1567661115 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22582077 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,RMVar_hsa_circ_36726 11654 RMVar_ID_11654 Human_SNP_ID_595874942 A-to-I Human chr16 + 15697590 15697590 15697590 GAAAAATGAGCCAGGCATGGTAGCATGTGCCTATAGTCCCAGCTACTCAGGAGGCTGAGGAAGGA GAAAAATGAGCCAGGCATGGTAGCATGTGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGAAGGA A G NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1033867002 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,RMVar_hsa_circ_36726 11655 RMVar_ID_11655 Human_SNP_ID_595875044 A-to-I Human chr16 + 15697876 15697876 15697876 TCGCCTAGGCTGGAGTGTAGTGGCATGATCTCAGCTCACTGCAACCTCTGCCTCCCAAGTCCAAG TCGCCTAGGCTGGAGTGTAGTGGCATGATCTCGGCTCACTGCAACCTCTGCCTCCCAAGTCCAAG A G NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs188363269 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,RMVar_hsa_circ_36726 11656 RMVar_ID_11656 Human_SNP_ID_595875104 A-to-I Human chr16 + 15698063 15698063 15698063 TGACATTGTGATCCACCCACCTCGGCCTCTCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCAA TGACATTGTGATCCACCCACCTCGGCCTCTCAGAGTGCTGGGATTACAGGCGTGAGCCACTGCAA A G NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1032745740 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,RMVar_hsa_circ_36726 11657 RMVar_ID_11657 Human_SNP_ID_595875105 A-to-I Human chr16 + 15698063 15698063 15698063 TGACATTGTGATCCACCCACCTCGGCCTCTCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCAA TGACATTGTGATCCACCCACCTCGGCCTCTCATAGTGCTGGGATTACAGGCGTGAGCCACTGCAA A T NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1032745740 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,RMVar_hsa_circ_36726 11658 RMVar_ID_11658 Human_SNP_ID_595875162 A-to-I Human chr16 + 15698270 15698270 15698270 AAAGAAAATCAGGGCCAGGCTCAGTGGCTCACACTTGTAATCCCAGCACTTTGGGAGGCTGAGGG AAAGAAAATCAGGGCCAGGCTCAGTGGCTCACGCTTGTAATCCCAGCACTTTGGGAGGCTGAGGG A G NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1001026322 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,RMVar_hsa_circ_36726 11659 RMVar_ID_11659 Human_SNP_ID_595875174 A-to-I Human chr16 + 15698317 15698317 15698317 ACTTTGGGAGGCTGAGGGCAGCGGATCAATTGAGCTCTGGAGGTTGAGGCCGCAGTGAGCCGTGT ACTTTGGGAGGCTGAGGGCAGCGGATCAATTGTGCTCTGGAGGTTGAGGCCGCAGTGAGCCGTGT A T NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs370790253 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,RMVar_hsa_circ_36726 11660 RMVar_ID_11660 Human_SNP_ID_595875258 A-to-I Human chr16 + 15698597 15698597 15698597 ATTTTTAGGCCAGGTGCAGTGAAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCAGAAGT ATTTTTAGGCCAGGTGCAGTGAAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCAGAAGT A G NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1027246169 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,RMVar_hsa_circ_36726 11661 RMVar_ID_11661 Human_SNP_ID_595875316 A-to-I Human chr16 + 15698789 15698789 15698789 TGGCTGAGGCACAAGAATCACTTGAACCCAGGAAGTGGAGGTTGCAGTGAGCCAAGATTGCACCA TGGCTGAGGCACAAGAATCACTTGAACCCAGGGAGTGGAGGTTGCAGTGAGCCAAGATTGCACCA A G NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1019448382 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,RMVar_hsa_circ_36726 11662 RMVar_ID_11662 Human_SNP_ID_595875319 A-to-I Human chr16 + 15698802 15698802 15698802 AGAATCACTTGAACCCAGGAAGTGGAGGTTGCAGTGAGCCAAGATTGCACCACTGAACTCCACTC AGAATCACTTGAACCCAGGAAGTGGAGGTTGCGGTGAGCCAAGATTGCACCACTGAACTCCACTC A G NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1026926850 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,RMVar_hsa_circ_36726 11663 RMVar_ID_11663 Human_SNP_ID_595875320 A-to-I Human chr16 + 15698810 15698810 15698810 TTGAACCCAGGAAGTGGAGGTTGCAGTGAGCCAAGATTGCACCACTGAACTCCACTCTGGGCAAC TTGAACCCAGGAAGTGGAGGTTGCAGTGAGCCGAGATTGCACCACTGAACTCCACTCTGGGCAAC A G NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1171280237 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17563994 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,RMVar_hsa_circ_36726 11664 RMVar_ID_11664 Human_SNP_ID_595875394 A-to-I Human chr16 + 15699024 15699024 15699024 TTCCTGCCTCAGCCTCCCAAGTAGCTGGGGCTACAGGTGCACACCACCACCCCTGGCTAATTTTT TTCCTGCCTCAGCCTCCCAAGTAGCTGGGGCTGCAGGTGCACACCACCACCCCTGGCTAATTTTT A G NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs943781234 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,RMVar_hsa_circ_36726 11665 RMVar_ID_11665 Human_SNP_ID_595875450 A-to-I Human chr16 + 15699240 15699240 15699240 CCCACCTTGACCTCCCAAGTGCTGGGGGTTACAAGCGTTAGCAATCATGCCTGGCCTTTTTTTTT CCCACCTTGACCTCCCAAGTGCTGGGGGTTACGAGCGTTAGCAATCATGCCTGGCCTTTTTTTTT A G NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1015441013 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,RMVar_hsa_circ_36726 11666 RMVar_ID_11666 Human_SNP_ID_595875799 A-to-I Human chr16 + 15700120 15700119 15700121 CGGTGATGAGGCTACCGTGTTGTTTTTGAGATAGAGTCTTGCTCTGTCACCCAGGCTGGAGTGTG CGGTGATGAGGCTACCGTGTTGTTTTTGAGAT__AGTCTTGCTCTGTCACCCAGGCTGGAGTGTG TAG T NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1237785263 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 11667 RMVar_ID_11667 Human_SNP_ID_595875800 A-to-I Human chr16 + 15700120 15700120 15700120 CGGTGATGAGGCTACCGTGTTGTTTTTGAGATAGAGTCTTGCTCTGTCACCCAGGCTGGAGTGTG CGGTGATGAGGCTACCGTGTTGTTTTTGAGATGGAGTCTTGCTCTGTCACCCAGGCTGGAGTGTG A G NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049283808 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 11668 RMVar_ID_11668 Human_SNP_ID_595875810 A-to-I Human chr16 + 15700166 15700166 15700166 TCACCCAGGCTGGAGTGTGGTGGCGTGATCTCAGCTCACTGCAACCTCCGCCTCCTGGGTTCAAA TCACCCAGGCTGGAGTGTGGTGGCGTGATCTCGGCTCACTGCAACCTCCGCCTCCTGGGTTCAAA A G NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,31158229,31158229,32596459 RNA-Seq:(High) rs979311884 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 11669 RMVar_ID_11669 Human_SNP_ID_595875925 A-to-I Human chr16 + 15700467 15700466 15700468 TTGGTCTTTTTTTTTTTTTTCTTTTTTGAGACAGAGTCATGCTCTTGCCCTGTCTTGTCCAGGCT TTGGTCTTTTTTTTTTTTTTCTTTTTTGAGAC__AGTCATGCTCTTGCCCTGTCTTGTCCAGGCT CAG C NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1050511463 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_18673630 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 11670 RMVar_ID_11670 Human_SNP_ID_595875927 A-to-I Human chr16 + 15700467 15700467 15700467 TTGGTCTTTTTTTTTTTTTTCTTTTTTGAGACAGAGTCATGCTCTTGCCCTGTCTTGTCCAGGCT TTGGTCTTTTTTTTTTTTTTCTTTTTTGAGACGGAGTCATGCTCTTGCCCTGTCTTGTCCAGGCT A G NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910630824 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18673630 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 11671 RMVar_ID_11671 Human_SNP_ID_595875941 A-to-I Human chr16 + 15700515 15700515 15700515 CCTGTCTTGTCCAGGCTGGAGTGTAGTGGTGCAATTTCGGCTCACCGCAGCCTCCGCCTCCTAGG CCTGTCTTGTCCAGGCTGGAGTGTAGTGGTGCGATTTCGGCTCACCGCAGCCTCCGCCTCCTAGG A G NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,31158229,32596459 RNA-Seq:(High) rs796662065 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8428239,Human_RBP_ID_12674003 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 11672 RMVar_ID_11672 Human_SNP_ID_595875962 A-to-I Human chr16 + 15700569 15700569 15700569 CGCCTCCTAGGTTCAAGCGATTCTCTTATCTCAGCTTCCCAAGTAGCTGGGACTACAGGAGTGTG CGCCTCCTAGGTTCAAGCGATTCTCTTATCTCGGCTTCCCAAGTAGCTGGGACTACAGGAGTGTG A G NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1307679703 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 11673 RMVar_ID_11673 Human_SNP_ID_595875983 A-to-I Human chr16 + 15700651 15700651 15700651 TTTGTATTTTTAGTGAGAAACGGGGTTTCACCATGTTGGCCATGCTGGTCTTGAACTCCCGGCCT TTTGTATTTTTAGTGAGAAACGGGGTTTCACCGTGTTGGCCATGCTGGTCTTGAACTCCCGGCCT A G NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs755512120 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 11674 RMVar_ID_11674 Human_SNP_ID_595876007 A-to-I Human chr16 + 15700703 15700703 15700703 GAACTCCCGGCCTCAAGTGATCCTCCCGCCTCAGCCTCCCAGAGTGCTGGAATTACAGGCCTGAG GAACTCCCGGCCTCAAGTGATCCTCCCGCCTCGGCCTCCCAGAGTGCTGGAATTACAGGCCTGAG A G NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1208251776 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 11675 RMVar_ID_11675 Human_SNP_ID_595876132 A-to-I Human chr16 + 15701114 15701114 15701114 AAAAAATTAGCTGGGTGCAGTGGTGCGTGCCTATAATTCCAGCTACTCCAGATGTTGAGGCAGGA AAAAAATTAGCTGGGTGCAGTGGTGCGTGCCTGTAATTCCAGCTACTCCAGATGTTGAGGCAGGA A G NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs570040827 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26444885,Human_RBP_ID_26938691 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 11676 RMVar_ID_11676 Human_SNP_ID_595879761 A-to-I Human chr16 - 15711831 15711831 15711831 AAAATTAGCCGGGTATGGTGGGGCGTGCCTGTAATCCCAGCTACTAGGGAGGCTGAGGCAGGAGA AAAATTAGCCGGGTATGGTGGGGCGTGCCTGTGATCCCAGCTACTAGGGAGGCTGAGGCAGGAGA T C MYH11 Ensembl:ENSG00000133392 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1188907415 Functional Loss SNV dbSNP153 33..33 33 - - - 11677 RMVar_ID_11677 Human_SNP_ID_595881177 A-to-I Human chr16 + 15715710 15715710 15715710 GCAGTGGTGCTCCAATGCCTGCTCTTCACCCTAGTTCATAGTTCACTGCAGCCTTGAACTCCTGG GCAGTGGTGCTCCAATGCCTGCTCTTCACCCTGGTTCATAGTTCACTGCAGCCTTGAACTCCTGG A G NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs993395816 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 11678 RMVar_ID_11678 Human_SNP_ID_595885589 A-to-I Human chr16 + 15727771 15727771 15727771 CAGGCAGAAGGATCGCTTAAGGCCAGGAGTACAAGACCAGCCTGGGCAATGTAGTGAGACCCCCA CAGGCAGAAGGATCGCTTAAGGCCAGGAGTACGAGACCAGCCTGGGCAATGTAGTGAGACCCCCA A G AF001548.2 Ensembl:ENSG00000263335 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs147979725 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 11679 RMVar_ID_11679 Human_SNP_ID_595888503 A-to-I Human chr16 + 15738335 15738335 15738335 TGAGACTAGACTGAGCATCATAGTGAAACCCCATCTCTACAAAATAAAAAATAAAAAAAAATTAG TGAGACTAGACTGAGCATCATAGTGAAACCCCGTCTCTACAAAATAAAAAATAAAAAAAAATTAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs974499691 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 11680 RMVar_ID_11680 Human_SNP_ID_595890541 A-to-I Human chr16 - 15745763 15745763 15745763 GGCCAACATGGGAAACCCCATCTCTACTAAAAATACAAAAATTAGCCAGGCATGGTTGTGGGCAC GGCCAACATGGGAAACCCCATCTCTACTAAAAGTACAAAAATTAGCCAGGCATGGTTGTGGGCAC T C MYH11 Ensembl:ENSG00000133392 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1356059127 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66563,RMVar_hsa_circ_67020,RMVar_hsa_circ_66887 11681 RMVar_ID_11681 Human_SNP_ID_595890795 A-to-I Human chr16 - 15746940 15746940 15746940 GGAATTAGAGGCGCCCACCACCACACTGGCCTAATTTTTGTATTTTTAGTAGAGACAAAGTTTCA GGAATTAGAGGCGCCCACCACCACACTGGCCTGATTTTTGTATTTTTAGTAGAGACAAAGTTTCA T C MYH11 Ensembl:ENSG00000133392 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1374730842 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66563,RMVar_hsa_circ_67020,RMVar_hsa_circ_66887 11682 RMVar_ID_11682 Human_SNP_ID_595890811 A-to-I Human chr16 - 15747001 15747001 15747001 TCACTGCAACCTCTGCCTCTTGGACTCAAGCAATTCTCGTGTCTGAGCCTCCCGAGTGGCTGGAA TCACTGCAACCTCTGCCTCTTGGACTCAAGCAGTTCTCGTGTCTGAGCCTCCCGAGTGGCTGGAA T C MYH11 Ensembl:ENSG00000133392 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1195407741 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66563,RMVar_hsa_circ_67020,RMVar_hsa_circ_66887 11683 RMVar_ID_11683 Human_SNP_ID_595923284 A-to-I Human chr16 - 15866921 15866921 15866921 TTACAGGTGTGAGCCACTGAGCCCAGCCATTTAGGAAGTATTATAAAGGCCCTTAAAGTTTGTAA TTACAGGTGTGAGCCACTGAGCCCAGCCATTTCGGAAGTATTATAAAGGCCCTTAAAGTTTGTAA T G FOPNL Ensembl:ENSG00000133393 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1240493660 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_468889,Human_RBP_ID_6495629,Human_RBP_ID_8186895,Human_RBP_ID_12674251,Human_RBP_ID_23679790,Human_RBP_ID_26445861 Human_miRNA_ID_1189086,Human_miRNA_ID_2508093,Human_miRNA_ID_2527298,Human_miRNA_ID_2530476,Human_miRNA_ID_2749600 RMVar_hsa_circ_176584,RMVar_hsa_circ_86798,RMVar_hsa_circ_89743,RMVar_hsa_circ_96121,RMVar_hsa_circ_176585,RMVar_hsa_circ_176586 11684 RMVar_ID_11684 Human_SNP_ID_595924712 A-to-I Human chr16 - 15872121 15872121 15872121 TTTAGTGGAGACAGGGTTTCCCTGTGTTAGCCAGGATGGTCTTGATCTCCTGACCTCATGATCCG TTTAGTGGAGACAGGGTTTCCCTGTGTTAGCCGGGATGGTCTTGATCTCCTGACCTCATGATCCG T C FOPNL Ensembl:ENSG00000133393 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1230660796 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_176584,RMVar_hsa_circ_86798,RMVar_hsa_circ_89743,RMVar_hsa_circ_96121,RMVar_hsa_circ_176585,RMVar_hsa_circ_176586 11685 RMVar_ID_11685 Human_SNP_ID_595925016 A-to-I Human chr16 - 15873232 15873231 15873239 TATAGAAGTATTTAAAACTCTGGGCTAGGCACAATGGCTCATGCCTGTAATCCCAGCAGTTTGGG TATAGAAGTATTTAAAACTCTGGGCCAGGCACAGTGGCTCATGCCTGTAATCCCAGCAGTTTGGG TTGTGCCTA CTGTGCCTG FOPNL Ensembl:ENSG00000133393 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs386789372 Functional Loss MNV dbSNP153 26..34 33 - - - Human_RBP_ID_12674378 RMVar_hsa_circ_176584,RMVar_hsa_circ_86798,RMVar_hsa_circ_89743,RMVar_hsa_circ_96121,RMVar_hsa_circ_176585,RMVar_hsa_circ_176586 11686 RMVar_ID_11686 Human_SNP_ID_595928396 A-to-I Human chr16 - 15885256 15885256 15885256 TCGCCCAGGCTAGAGTGCAGTGGCACCACCTCAGCTCACTGCACCCTCCACCTCCCAGGTTCAAG TCGCCCAGGCTAGAGTGCAGTGGCACCACCTCGGCTCACTGCACCCTCCACCTCCCAGGTTCAAG T C FOPNL Ensembl:ENSG00000133393 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs55643565 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82152,RMVar_hsa_circ_106198,RMVar_hsa_circ_176589,RMVar_hsa_circ_176590 11687 RMVar_ID_11687 Human_SNP_ID_595928502 A-to-I Human chr16 - 15885563 15885563 15885563 CATAGTGAAACCCTGTCTCTACTAAAAATACAAAAATTAGCCAGTCGTGGTATCGCACACCTGTA CATAGTGAAACCCTGTCTCTACTAAAAATACACAAATTAGCCAGTCGTGGTATCGCACACCTGTA T G FOPNL Ensembl:ENSG00000133393 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1209081077 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82152,RMVar_hsa_circ_106198,RMVar_hsa_circ_176589,RMVar_hsa_circ_176590 11688 RMVar_ID_11688 Human_SNP_ID_595947807 A-to-I Human chr16 + 15952839 15952839 15952839 ATTGCTTGAGGTCAGGAGTTCGAGACCAGCCTAGGCAACATGGATTGACCCCCGTCTCTACTAAT ATTGCTTGAGGTCAGGAGTTCGAGACCAGCCTGGGCAACATGGATTGACCCCCGTCTCTACTAAT A G ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474654018 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 11689 RMVar_ID_11689 Human_SNP_ID_595947885 A-to-I Human chr16 + 15953067 15953067 15953067 CCTGTCTCAAAAAAAAGAGGGCCGGGTGTAGTAGATCATGCCTGTAATCCCAGCACTTTGGGAGG CCTGTCTCAAAAAAAAGAGGGCCGGGTGTAGTGGATCATGCCTGTAATCCCAGCACTTTGGGAGG A G ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1309106064 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 11690 RMVar_ID_11690 Human_SNP_ID_595947956 A-to-I Human chr16 + 15953274 15953274 15953274 AGGAGAATTGCTTGAACCTGGGAAGAGGTTGCAGTGAGCTGAGATCACATCACTGCACTCCAACC AGGAGAATTGCTTGAACCTGGGAAGAGGTTGCGGTGAGCTGAGATCACATCACTGCACTCCAACC A G ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs931387306 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 11691 RMVar_ID_11691 Human_SNP_ID_595948208 A-to-I Human chr16 + 15954085 15954085 15954085 GCTAGGGTGCAGTGGTGTGATCTCGGTTCACTACAACCTCTGCCTGCTGCGTTCACATGATTCCC GCTAGGGTGCAGTGGTGTGATCTCGGTTCACTGCAACCTCTGCCTGCTGCGTTCACATGATTCCC A G ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1276247182 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 11692 RMVar_ID_11692 Human_SNP_ID_595951629 A-to-I Human chr16 + 15966790 15966790 15966790 TTCCTGCCTTACCCTCCCGAGTGTCTTGGATTATAGATGCTTGTCAACATGCCCAGCTAATTTTT TTCCTGCCTTACCCTCCCGAGTGTCTTGGATTGTAGATGCTTGTCAACATGCCCAGCTAATTTTT A G ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs533737411 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 11693 RMVar_ID_11693 Human_SNP_ID_595952105 A-to-I Human chr16 + 15968444 15968436 15968444 TAATTTTTTTTTTTGAGACAGAGTCTTGCTCTATTACCCAGGCTGGAGTGCAGGTGGCGTGATCT TAATTTTTTTTTTTGAGACAGAGTC________TTACCCAGGCTGGAGTGCAGGTGGCGTGATCT CTTGCTCTA C ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1375955414 Functional Loss DEL dbSNP153 26..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 11694 RMVar_ID_11694 Human_SNP_ID_595952109 A-to-I Human chr16 + 15968444 15968444 15968444 TAATTTTTTTTTTTGAGACAGAGTCTTGCTCTATTACCCAGGCTGGAGTGCAGGTGGCGTGATCT TAATTTTTTTTTTTGAGACAGAGTCTTGCTCTGTTACCCAGGCTGGAGTGCAGGTGGCGTGATCT A G ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs921630640 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 11695 RMVar_ID_11695 Human_SNP_ID_595952127 A-to-I Human chr16 + 15968510 15968510 15968510 TGCTCACTGCAGCCTTCACCTGCCGAGTAGCTAGGACTGCAGGCATGCACCACTATGTCTAGCTA TGCTCACTGCAGCCTTCACCTGCCGAGTAGCTGGGACTGCAGGCATGCACCACTATGTCTAGCTA A G ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1365915174 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 11696 RMVar_ID_11696 Human_SNP_ID_595964759 A-to-I Human chr16 + 16011043 16011043 16011043 ATCACTTGAGGTCGGGAATTTGAGACCAGTATAGCCAACATGGCAAAACCCCGTCTCTACTAAAA ATCACTTGAGGTCGGGAATTTGAGACCAGTATGGCCAACATGGCAAAACCCCGTCTCTACTAAAA A G ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1256552124 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_125227,RMVar_hsa_circ_176594,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_285203,RMVar_hsa_circ_88994,RMVar_hsa_circ_276112,RMVar_hsa_circ_64508,RMVar_hsa_circ_176596,RMVar_hsa_circ_176600,RMVar_hsa_circ_176602,RMVar_hsa_circ_176604,RMVar_hsa_circ_176603,RMVar_hsa_circ_176601,RMVar_hsa_circ_176598,RMVar_hsa_circ_176599,RMVar_hsa_circ_176597,RMVar_hsa_circ_176608,RMVar_hsa_circ_116070,RMVar_hsa_circ_298290,RMVar_hsa_circ_341552,RMVar_hsa_circ_176610,RMVar_hsa_circ_94441,RMVar_hsa_circ_176609 11697 RMVar_ID_11697 Human_SNP_ID_595964773 A-to-I Human chr16 + 16011087 16011087 16011087 AAAACCCCGTCTCTACTAAAAATAAAAAAATTAGCCGGCGTGGTGGCACACGCCTGTAGTCCTAG AAAACCCCGTCTCTACTAAAAATAAAAAAATTCGCCGGCGTGGTGGCACACGCCTGTAGTCCTAG A C ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs907047634 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_125227,RMVar_hsa_circ_176594,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_285203,RMVar_hsa_circ_88994,RMVar_hsa_circ_276112,RMVar_hsa_circ_64508,RMVar_hsa_circ_176596,RMVar_hsa_circ_176600,RMVar_hsa_circ_176602,RMVar_hsa_circ_176604,RMVar_hsa_circ_176603,RMVar_hsa_circ_176601,RMVar_hsa_circ_176598,RMVar_hsa_circ_176599,RMVar_hsa_circ_176597,RMVar_hsa_circ_176608,RMVar_hsa_circ_116070,RMVar_hsa_circ_298290,RMVar_hsa_circ_341552,RMVar_hsa_circ_176610,RMVar_hsa_circ_94441,RMVar_hsa_circ_176609 11698 RMVar_ID_11698 Human_SNP_ID_595965058 A-to-I Human chr16 + 16012070 16012070 16012070 GTGATCCTCCTGTCTGGGCCTCCTAAAGTGCTAGGATTATAGGTGTGAGCCACCATGCCCTGCCC GTGATCCTCCTGTCTGGGCCTCCTAAAGTGCTCGGATTATAGGTGTGAGCCACCATGCCCTGCCC A C ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs367888948 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_125227,RMVar_hsa_circ_176594,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_285203,RMVar_hsa_circ_88994,RMVar_hsa_circ_276112,RMVar_hsa_circ_64508,RMVar_hsa_circ_176596,RMVar_hsa_circ_176600,RMVar_hsa_circ_176602,RMVar_hsa_circ_176604,RMVar_hsa_circ_176603,RMVar_hsa_circ_176601,RMVar_hsa_circ_176598,RMVar_hsa_circ_176599,RMVar_hsa_circ_176597,RMVar_hsa_circ_176608,RMVar_hsa_circ_116070,RMVar_hsa_circ_298290,RMVar_hsa_circ_341552,RMVar_hsa_circ_176610,RMVar_hsa_circ_94441,RMVar_hsa_circ_176609 11699 RMVar_ID_11699 Human_SNP_ID_595965223 A-to-I Human chr16 + 16012549 16012549 16012549 TAGAGACAGGGTCTTTCCATGTTGCCCAGGCTAGTCTTAAACTCCCGAGCCCAAGTGATCCCTCT TAGAGACAGGGTCTTTCCATGTTGCCCAGGCTGGTCTTAAACTCCCGAGCCCAAGTGATCCCTCT A G ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1479472248 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_125227,RMVar_hsa_circ_176594,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_285203,RMVar_hsa_circ_88994,RMVar_hsa_circ_276112,RMVar_hsa_circ_64508,RMVar_hsa_circ_176596,RMVar_hsa_circ_176600,RMVar_hsa_circ_176602,RMVar_hsa_circ_176604,RMVar_hsa_circ_176603,RMVar_hsa_circ_176601,RMVar_hsa_circ_176598,RMVar_hsa_circ_176599,RMVar_hsa_circ_176597,RMVar_hsa_circ_176608,RMVar_hsa_circ_116070,RMVar_hsa_circ_298290,RMVar_hsa_circ_341552,RMVar_hsa_circ_176610,RMVar_hsa_circ_94441,RMVar_hsa_circ_176609 11700 RMVar_ID_11700 Human_SNP_ID_595966769 A-to-I Human chr16 + 16017370 16017370 16017370 TTCCTACCTCAGCTTTCTGAGTAGCTGGAATTACAGGCACACACCACCATGCCTGGCTAATTTTT TTCCTACCTCAGCTTTCTGAGTAGCTGGAATTGCAGGCACACACCACCATGCCTGGCTAATTTTT A G ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1174385751 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 11701 RMVar_ID_11701 Human_SNP_ID_595967321 A-to-I Human chr16 + 16019365 16019365 16019365 ACCTCAAGTGATCCACCCGCCTCGGCCTCCCAAAATGTTGGGATTACAGGTGTGAGCCACCGTGT ACCTCAAGTGATCCACCCGCCTCGGCCTCCCAGAATGTTGGGATTACAGGTGTGAGCCACCGTGT A G ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1030889919 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 11702 RMVar_ID_11702 Human_SNP_ID_595967322 A-to-I Human chr16 + 16019365 16019365 16019365 ACCTCAAGTGATCCACCCGCCTCGGCCTCCCAAAATGTTGGGATTACAGGTGTGAGCCACCGTGT ACCTCAAGTGATCCACCCGCCTCGGCCTCCCATAATGTTGGGATTACAGGTGTGAGCCACCGTGT A T ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1030889919 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 11703 RMVar_ID_11703 Human_SNP_ID_595968236 A-to-I Human chr16 + 16022960 16022960 16022960 TTGAGATAGGGTCTCACTCTGTCTCGCAGACTAGAGTGCAGTGGTGTGATCATAGCTCACTGCAG TTGAGATAGGGTCTCACTCTGTCTCGCAGACTGGAGTGCAGTGGTGTGATCATAGCTCACTGCAG A G ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749525626 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 11704 RMVar_ID_11704 Human_SNP_ID_595968268 A-to-I Human chr16 + 16023086 16023086 16023086 CAGGTGCACACTACTGTGTTTGGCTAATTTTTAAATTTTTTGTAGGCGTGAGGGCTCCTTATGTT CAGGTGCACACTACTGTGTTTGGCTAATTTTTTAATTTTTTGTAGGCGTGAGGGCTCCTTATGTT A T ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs967135005 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 11705 RMVar_ID_11705 Human_SNP_ID_595968278 A-to-I Human chr16 + 16023123 16023123 16023123 TTTTGTAGGCGTGAGGGCTCCTTATGTTGCCCAGTCTGGTCTTGAACTCCTGGCCTCAAGCCATC TTTTGTAGGCGTGAGGGCTCCTTATGTTGCCCCGTCTGGTCTTGAACTCCTGGCCTCAAGCCATC A C ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1399484036 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 11706 RMVar_ID_11706 Human_SNP_ID_595968288 A-to-I Human chr16 + 16023188 16023188 16023188 CTCCCACCTCAGCCTCCCAAAATACTGGGATTACAGGCCTGAGCCACTGAACCTAGTTTTTTTGA CTCCCACCTCAGCCTCCCAAAATACTGGGATTCCAGGCCTGAGCCACTGAACCTAGTTTTTTTGA A C ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs531910335 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 11707 RMVar_ID_11707 Human_SNP_ID_595968665 A-to-I Human chr16 + 16024513 16024513 16024513 AGCTGGGACCATAGTTGCGTGCCACCACGCCCAAGTAACTTTTTCTGTTTTTGGTAGAGATGGGG AGCTGGGACCATAGTTGCGTGCCACCACGCCCGAGTAACTTTTTCTGTTTTTGGTAGAGATGGGG A G ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1396549109 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 11708 RMVar_ID_11708 Human_SNP_ID_595968666 A-to-I Human chr16 + 16024513 16024513 16024513 AGCTGGGACCATAGTTGCGTGCCACCACGCCCAAGTAACTTTTTCTGTTTTTGGTAGAGATGGGG AGCTGGGACCATAGTTGCGTGCCACCACGCCCTAGTAACTTTTTCTGTTTTTGGTAGAGATGGGG A T ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1396549109 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 11709 RMVar_ID_11709 Human_SNP_ID_595968682 A-to-I Human chr16 + 16024587 16024587 16024587 GTTACTCAGGCTGGTCTTGAACTCCTGAGCTCAAGTGATGCCCTGCCTTGGCCTCCCAAAATGCT GTTACTCAGGCTGGTCTTGAACTCCTGAGCTCCAGTGATGCCCTGCCTTGGCCTCCCAAAATGCT A C ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1442442891 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 11710 RMVar_ID_11710 Human_SNP_ID_595968683 A-to-I Human chr16 + 16024587 16024587 16024587 GTTACTCAGGCTGGTCTTGAACTCCTGAGCTCAAGTGATGCCCTGCCTTGGCCTCCCAAAATGCT GTTACTCAGGCTGGTCTTGAACTCCTGAGCTCGAGTGATGCCCTGCCTTGGCCTCCCAAAATGCT A G ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1442442891 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 11711 RMVar_ID_11711 Human_SNP_ID_595969936 A-to-I Human chr16 + 16029034 16029034 16029034 GGGTTGGGGCCCTAGGCACTTGGCACTTAACAAACTCCTTAGGTGATTCCAGTGGACAGGCAGGG GGGTTGGGGCCCTAGGCACTTGGCACTTAACAGACTCCTTAGGTGATTCCAGTGGACAGGCAGGG A G ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs144445149 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 11712 RMVar_ID_11712 Human_SNP_ID_595971213 A-to-I Human chr16 + 16033753 16033752 16033753 TCAAGCGATTCTCCTGCCTCAGCCTCCCAGGTAGCTGGGATTACAGGCTTGCGCCACCATGCCCG TCAAGCGATTCTCCTGCCTCAGCCTCCCAGGT_GCTGGGATTACAGGCTTGCGCCACCATGCCCG TA T ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1309762398 Functional Loss DEL 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_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_176620,RMVar_hsa_circ_176622,RMVar_hsa_circ_176623,RMVar_hsa_circ_176624,RMVar_hsa_circ_176621 11713 RMVar_ID_11713 Human_SNP_ID_595971214 A-to-I Human chr16 + 16033753 16033753 16033753 TCAAGCGATTCTCCTGCCTCAGCCTCCCAGGTAGCTGGGATTACAGGCTTGCGCCACCATGCCCG TCAAGCGATTCTCCTGCCTCAGCCTCCCAGGTTGCTGGGATTACAGGCTTGCGCCACCATGCCCG A T ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1211980992 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_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_176620,RMVar_hsa_circ_176622,RMVar_hsa_circ_176623,RMVar_hsa_circ_176624,RMVar_hsa_circ_176621 11714 RMVar_ID_11714 Human_SNP_ID_595971522 A-to-I Human chr16 + 16034705 16034705 16034705 TGCTTCCTGGGTTCAAGAGATTCTCCTGTCTCAGCCTCCTGAGTAGCTGGGATTACAGGGACCTG TGCTTCCTGGGTTCAAGAGATTCTCCTGTCTCGGCCTCCTGAGTAGCTGGGATTACAGGGACCTG A G ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1360488846 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_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_176620,RMVar_hsa_circ_176622,RMVar_hsa_circ_176623,RMVar_hsa_circ_176624,RMVar_hsa_circ_176621 11715 RMVar_ID_11715 Human_SNP_ID_595971646 A-to-I Human chr16 + 16035237 16035236 16035237 CAGCCTGGCCTACATGGTGAAACCCTGTCTCCACTAACAATACAAAAATTAGCCGGGCAGCACAC CAGCCTGGCCTACATGGTGAAACCCTGTCTCC_CTAACAATACAAAAATTAGCCGGGCAGCACAC CA C ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1174968507 Functional Loss DEL 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_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_176620,RMVar_hsa_circ_176622,RMVar_hsa_circ_176623,RMVar_hsa_circ_176624,RMVar_hsa_circ_176621 11716 RMVar_ID_11716 Human_SNP_ID_595971781 A-to-I Human chr16 + 16035680 16035680 16035680 GACTGGCTAATTTTTTTATTTTTACTTTTCGTAGAGATAGTCTCCCTATGTTGTCCAGGCTGGTC GACTGGCTAATTTTTTTATTTTTACTTTTCGTCGAGATAGTCTCCCTATGTTGTCCAGGCTGGTC A C ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs906658576 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_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_176620,RMVar_hsa_circ_176622,RMVar_hsa_circ_176623,RMVar_hsa_circ_176624,RMVar_hsa_circ_176621 11717 RMVar_ID_11717 Human_SNP_ID_595971813 A-to-I Human chr16 + 16035763 16035763 16035763 AAAATCCTCCCACCTCGGCCTCCCAGAGCGCTAGGATTATAGACATGAGCTACCGTGCCTGGCCC AAAATCCTCCCACCTCGGCCTCCCAGAGCGCTGGGATTATAGACATGAGCTACCGTGCCTGGCCC A G ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs936481798 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_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_176620,RMVar_hsa_circ_176622,RMVar_hsa_circ_176623,RMVar_hsa_circ_176624,RMVar_hsa_circ_176621 11718 RMVar_ID_11718 Human_SNP_ID_595971879 A-to-I Human chr16 + 16035977 16035977 16035977 TCTCTACAAAAATAAAAAATAAAAAAAAAATTAGCCAGTCATAATGGCTTACACCCAAAGTCCCA TCTCTACAAAAATAAAAAATAAAAAAAAAATTGGCCAGTCATAATGGCTTACACCCAAAGTCCCA A G ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs577745170 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_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_176620,RMVar_hsa_circ_176622,RMVar_hsa_circ_176623,RMVar_hsa_circ_176624,RMVar_hsa_circ_176621 11719 RMVar_ID_11719 Human_SNP_ID_595976511 A-to-I Human chr16 + 16051310 16051310 16051310 TCCCACTTTGTCATCTCATCTAGCTGGGGACTACAGGTGCACGCCACCATGCCTGGCTAAGTTAT TCCCACTTTGTCATCTCATCTAGCTGGGGACTGCAGGTGCACGCCACCATGCCTGGCTAAGTTAT A G ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1567350715 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_315,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_176612,RMVar_hsa_circ_79332,RMVar_hsa_circ_84030,RMVar_hsa_circ_176613,RMVar_hsa_circ_91416,RMVar_hsa_circ_176611,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_17801,RMVar_hsa_circ_279065,RMVar_hsa_circ_15940,RMVar_hsa_circ_176620,RMVar_hsa_circ_176622,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_344358,RMVar_hsa_circ_372789,RMVar_hsa_circ_373331,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_176633,RMVar_hsa_circ_176631,RMVar_hsa_circ_126019,RMVar_hsa_circ_176637,RMVar_hsa_circ_87122,RMVar_hsa_circ_103635,RMVar_hsa_circ_176636,RMVar_hsa_circ_176638 11720 RMVar_ID_11720 Human_SNP_ID_595977348 A-to-I Human chr16 + 16054155 16054155 16054155 CACCACCACACCCAGCTAATCTTTGTATTTTTAGTAGAGATGAGGCTTTACCACATTGGCCAGGC CACCACCACACCCAGCTAATCTTTGTATTTTTGGTAGAGATGAGGCTTTACCACATTGGCCAGGC A G ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs996337927 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_315,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_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_176612,RMVar_hsa_circ_79332,RMVar_hsa_circ_84030,RMVar_hsa_circ_176613,RMVar_hsa_circ_91416,RMVar_hsa_circ_176611,RMVar_hsa_circ_88330,RMVar_hsa_circ_176618,RMVar_hsa_circ_37879,RMVar_hsa_circ_176619,RMVar_hsa_circ_370295,RMVar_hsa_circ_17801,RMVar_hsa_circ_279065,RMVar_hsa_circ_15940,RMVar_hsa_circ_176620,RMVar_hsa_circ_176621,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_23834,RMVar_hsa_circ_344358,RMVar_hsa_circ_373331,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_176633,RMVar_hsa_circ_176631,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_176640,RMVar_hsa_circ_320715,RMVar_hsa_circ_362131,RMVar_hsa_circ_289182,RMVar_hsa_circ_176639 11721 RMVar_ID_11721 Human_SNP_ID_595978356 A-to-I Human chr16 + 16057795 16057795 16057795 TTCATTTTAGTTTTTTGGGGGGTTTTGTTTTGAAATGGGGTCTCGCTCTGTCCCCCAGGCTGGAG TTCATTTTAGTTTTTTGGGGGGTTTTGTTTTGGAATGGGGTCTCGCTCTGTCCCCCAGGCTGGAG A G ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs56267834 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_315,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_88994,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_176612,RMVar_hsa_circ_79332,RMVar_hsa_circ_91416,RMVar_hsa_circ_176611,RMVar_hsa_circ_88330,RMVar_hsa_circ_176618,RMVar_hsa_circ_176619,RMVar_hsa_circ_370295,RMVar_hsa_circ_17801,RMVar_hsa_circ_15940,RMVar_hsa_circ_176620,RMVar_hsa_circ_77185,RMVar_hsa_circ_94162,RMVar_hsa_circ_176628,RMVar_hsa_circ_176629,RMVar_hsa_circ_23834,RMVar_hsa_circ_344358,RMVar_hsa_circ_373331,RMVar_hsa_circ_337336,RMVar_hsa_circ_113461,RMVar_hsa_circ_122709,RMVar_hsa_circ_29310,RMVar_hsa_circ_176630,RMVar_hsa_circ_176632,RMVar_hsa_circ_176631,RMVar_hsa_circ_126019,RMVar_hsa_circ_5960,RMVar_hsa_circ_176637,RMVar_hsa_circ_87122,RMVar_hsa_circ_103635,RMVar_hsa_circ_176636,RMVar_hsa_circ_176638,RMVar_hsa_circ_91549,RMVar_hsa_circ_176640,RMVar_hsa_circ_320715,RMVar_hsa_circ_362131,RMVar_hsa_circ_81981,RMVar_hsa_circ_176642,RMVar_hsa_circ_176643 11722 RMVar_ID_11722 Human_SNP_ID_595980720 A-to-I Human chr16 + 16066689 16066689 16066689 GGGAGGCCGAGGCAGACGGATCACTTGAGGCCAGGAGCTCAAGACCAGCCTGACCAACATGGCGA GGGAGGCCGAGGCAGACGGATCACTTGAGGCCGGGAGCTCAAGACCAGCCTGACCAACATGGCGA A G ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1239251486 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_315,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_88994,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_176612,RMVar_hsa_circ_79332,RMVar_hsa_circ_91416,RMVar_hsa_circ_176611,RMVar_hsa_circ_88330,RMVar_hsa_circ_176618,RMVar_hsa_circ_176619,RMVar_hsa_circ_370295,RMVar_hsa_circ_17801,RMVar_hsa_circ_15940,RMVar_hsa_circ_176620,RMVar_hsa_circ_77185,RMVar_hsa_circ_94162,RMVar_hsa_circ_176628,RMVar_hsa_circ_176629,RMVar_hsa_circ_23834,RMVar_hsa_circ_344358,RMVar_hsa_circ_373331,RMVar_hsa_circ_337336,RMVar_hsa_circ_113461,RMVar_hsa_circ_122709,RMVar_hsa_circ_29310,RMVar_hsa_circ_176630,RMVar_hsa_circ_176632,RMVar_hsa_circ_176631,RMVar_hsa_circ_126019,RMVar_hsa_circ_5960,RMVar_hsa_circ_176637,RMVar_hsa_circ_87122,RMVar_hsa_circ_103635,RMVar_hsa_circ_176636,RMVar_hsa_circ_176638,RMVar_hsa_circ_91549,RMVar_hsa_circ_176640,RMVar_hsa_circ_320715,RMVar_hsa_circ_362131,RMVar_hsa_circ_81981,RMVar_hsa_circ_176642,RMVar_hsa_circ_176643 11723 RMVar_ID_11723 Human_SNP_ID_595981587 A-to-I Human chr16 + 16069294 16069294 16069294 GACTCAGAAGGCTGGGGTGGGAGGATCAGCTGAGCTTGGGAAGTTGAGGCTGCAGTGAGTCATAG GACTCAGAAGGCTGGGGTGGGAGGATCAGCTGGGCTTGGGAAGTTGAGGCTGCAGTGAGTCATAG A G ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1161749953 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_315,RMVar_hsa_circ_279614,RMVar_hsa_circ_351085,RMVar_hsa_circ_373070,RMVar_hsa_circ_370458,RMVar_hsa_circ_362371,RMVar_hsa_circ_88994,RMVar_hsa_circ_176596,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_79332,RMVar_hsa_circ_91416,RMVar_hsa_circ_176611,RMVar_hsa_circ_88330,RMVar_hsa_circ_176618,RMVar_hsa_circ_176619,RMVar_hsa_circ_370295,RMVar_hsa_circ_15940,RMVar_hsa_circ_176620,RMVar_hsa_circ_77185,RMVar_hsa_circ_94162,RMVar_hsa_circ_176628,RMVar_hsa_circ_176629,RMVar_hsa_circ_344358,RMVar_hsa_circ_373331,RMVar_hsa_circ_337336,RMVar_hsa_circ_113461,RMVar_hsa_circ_122709,RMVar_hsa_circ_29310,RMVar_hsa_circ_176630,RMVar_hsa_circ_176632,RMVar_hsa_circ_176631,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_91549,RMVar_hsa_circ_176640,RMVar_hsa_circ_320715,RMVar_hsa_circ_81981,RMVar_hsa_circ_34386,RMVar_hsa_circ_125055,RMVar_hsa_circ_176642,RMVar_hsa_circ_176643,RMVar_hsa_circ_316705,RMVar_hsa_circ_374663,RMVar_hsa_circ_313349,RMVar_hsa_circ_100014,RMVar_hsa_circ_107296,RMVar_hsa_circ_176644,RMVar_hsa_circ_176646,RMVar_hsa_circ_176648,RMVar_hsa_circ_176647,RMVar_hsa_circ_176645 11724 RMVar_ID_11724 Human_SNP_ID_595982524 A-to-I Human chr16 + 16072374 16072374 16072374 TTGGATAATATTTTGGTATGTTTTGTAGAGACAGGGTTTCACCATGTTGTCCAGGCCGGTCTCGA TTGGATAATATTTTGGTATGTTTTGTAGAGACGGGGTTTCACCATGTTGTCCAGGCCGGTCTCGA A G ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs201834272 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_315,RMVar_hsa_circ_279614,RMVar_hsa_circ_351085,RMVar_hsa_circ_373070,RMVar_hsa_circ_362371,RMVar_hsa_circ_88994,RMVar_hsa_circ_176596,RMVar_hsa_circ_176598,RMVar_hsa_circ_176597,RMVar_hsa_circ_176610,RMVar_hsa_circ_94441,RMVar_hsa_circ_79332,RMVar_hsa_circ_91416,RMVar_hsa_circ_176611,RMVar_hsa_circ_88330,RMVar_hsa_circ_176618,RMVar_hsa_circ_176619,RMVar_hsa_circ_15940,RMVar_hsa_circ_77185,RMVar_hsa_circ_94162,RMVar_hsa_circ_176628,RMVar_hsa_circ_176629,RMVar_hsa_circ_344358,RMVar_hsa_circ_337336,RMVar_hsa_circ_113461,RMVar_hsa_circ_122709,RMVar_hsa_circ_29310,RMVar_hsa_circ_176630,RMVar_hsa_circ_176631,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_91549,RMVar_hsa_circ_81981,RMVar_hsa_circ_34386,RMVar_hsa_circ_125055,RMVar_hsa_circ_176642,RMVar_hsa_circ_176643,RMVar_hsa_circ_316705,RMVar_hsa_circ_374663,RMVar_hsa_circ_100014,RMVar_hsa_circ_107296,RMVar_hsa_circ_176644,RMVar_hsa_circ_176646,RMVar_hsa_circ_176647,RMVar_hsa_circ_176645,RMVar_hsa_circ_106446,RMVar_hsa_circ_286548,RMVar_hsa_circ_47523,RMVar_hsa_circ_176651 11725 RMVar_ID_11725 Human_SNP_ID_595982666 A-to-I Human chr16 + 16072858 16072858 16072858 GAGGTCAGGAGTTCGAGATCAGCCTGGCCAACAAGGTGAAACCCCGTCTCTACTGAAAATACAAA GAGGTCAGGAGTTCGAGATCAGCCTGGCCAACGAGGTGAAACCCCGTCTCTACTGAAAATACAAA A G ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1231178653 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_315,RMVar_hsa_circ_279614,RMVar_hsa_circ_351085,RMVar_hsa_circ_373070,RMVar_hsa_circ_362371,RMVar_hsa_circ_88994,RMVar_hsa_circ_176596,RMVar_hsa_circ_176598,RMVar_hsa_circ_176597,RMVar_hsa_circ_176610,RMVar_hsa_circ_94441,RMVar_hsa_circ_79332,RMVar_hsa_circ_91416,RMVar_hsa_circ_176611,RMVar_hsa_circ_88330,RMVar_hsa_circ_176618,RMVar_hsa_circ_176619,RMVar_hsa_circ_15940,RMVar_hsa_circ_77185,RMVar_hsa_circ_94162,RMVar_hsa_circ_176628,RMVar_hsa_circ_176629,RMVar_hsa_circ_344358,RMVar_hsa_circ_337336,RMVar_hsa_circ_113461,RMVar_hsa_circ_122709,RMVar_hsa_circ_29310,RMVar_hsa_circ_176630,RMVar_hsa_circ_176631,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_91549,RMVar_hsa_circ_81981,RMVar_hsa_circ_34386,RMVar_hsa_circ_125055,RMVar_hsa_circ_176642,RMVar_hsa_circ_176643,RMVar_hsa_circ_316705,RMVar_hsa_circ_374663,RMVar_hsa_circ_100014,RMVar_hsa_circ_107296,RMVar_hsa_circ_176644,RMVar_hsa_circ_176646,RMVar_hsa_circ_176647,RMVar_hsa_circ_176645,RMVar_hsa_circ_106446,RMVar_hsa_circ_286548,RMVar_hsa_circ_47523,RMVar_hsa_circ_176651 11726 RMVar_ID_11726 Human_SNP_ID_595982892 A-to-I Human chr16 + 16073501 16073501 16073501 AAGTGAGGCACAGGCTGGGTGCAGTGGCTCCTACCTATAATCCTAGTACTTTGGGAGGCCAAGGC AAGTGAGGCACAGGCTGGGTGCAGTGGCTCCTGCCTATAATCCTAGTACTTTGGGAGGCCAAGGC A G ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1256319988 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_315,RMVar_hsa_circ_279614,RMVar_hsa_circ_351085,RMVar_hsa_circ_373070,RMVar_hsa_circ_362371,RMVar_hsa_circ_88994,RMVar_hsa_circ_176596,RMVar_hsa_circ_176598,RMVar_hsa_circ_176597,RMVar_hsa_circ_176610,RMVar_hsa_circ_94441,RMVar_hsa_circ_79332,RMVar_hsa_circ_91416,RMVar_hsa_circ_176611,RMVar_hsa_circ_88330,RMVar_hsa_circ_176618,RMVar_hsa_circ_176619,RMVar_hsa_circ_15940,RMVar_hsa_circ_77185,RMVar_hsa_circ_94162,RMVar_hsa_circ_176628,RMVar_hsa_circ_176629,RMVar_hsa_circ_344358,RMVar_hsa_circ_337336,RMVar_hsa_circ_113461,RMVar_hsa_circ_122709,RMVar_hsa_circ_29310,RMVar_hsa_circ_176630,RMVar_hsa_circ_176631,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_91549,RMVar_hsa_circ_81981,RMVar_hsa_circ_34386,RMVar_hsa_circ_125055,RMVar_hsa_circ_176642,RMVar_hsa_circ_176643,RMVar_hsa_circ_316705,RMVar_hsa_circ_374663,RMVar_hsa_circ_100014,RMVar_hsa_circ_107296,RMVar_hsa_circ_176644,RMVar_hsa_circ_176646,RMVar_hsa_circ_176647,RMVar_hsa_circ_176645,RMVar_hsa_circ_106446,RMVar_hsa_circ_286548,RMVar_hsa_circ_47523,RMVar_hsa_circ_176651 11727 RMVar_ID_11727 Human_SNP_ID_595982950 A-to-I Human chr16 + 16073677 16073677 16073677 TACTTGAGAGGCTGAGGCAGGAGGATTGGCTGAGCCCGGGAGTTCAAGGCTATAGTGAGCTATGA TACTTGAGAGGCTGAGGCAGGAGGATTGGCTGGGCCCGGGAGTTCAAGGCTATAGTGAGCTATGA A G ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs960602988 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_315,RMVar_hsa_circ_279614,RMVar_hsa_circ_351085,RMVar_hsa_circ_373070,RMVar_hsa_circ_362371,RMVar_hsa_circ_88994,RMVar_hsa_circ_176596,RMVar_hsa_circ_176598,RMVar_hsa_circ_176597,RMVar_hsa_circ_176610,RMVar_hsa_circ_94441,RMVar_hsa_circ_79332,RMVar_hsa_circ_91416,RMVar_hsa_circ_176611,RMVar_hsa_circ_88330,RMVar_hsa_circ_176618,RMVar_hsa_circ_176619,RMVar_hsa_circ_15940,RMVar_hsa_circ_77185,RMVar_hsa_circ_94162,RMVar_hsa_circ_176628,RMVar_hsa_circ_176629,RMVar_hsa_circ_344358,RMVar_hsa_circ_337336,RMVar_hsa_circ_113461,RMVar_hsa_circ_122709,RMVar_hsa_circ_29310,RMVar_hsa_circ_176630,RMVar_hsa_circ_176631,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_91549,RMVar_hsa_circ_81981,RMVar_hsa_circ_34386,RMVar_hsa_circ_125055,RMVar_hsa_circ_176642,RMVar_hsa_circ_176643,RMVar_hsa_circ_316705,RMVar_hsa_circ_374663,RMVar_hsa_circ_100014,RMVar_hsa_circ_107296,RMVar_hsa_circ_176644,RMVar_hsa_circ_176646,RMVar_hsa_circ_176647,RMVar_hsa_circ_176645,RMVar_hsa_circ_106446,RMVar_hsa_circ_286548,RMVar_hsa_circ_47523,RMVar_hsa_circ_176651 11728 RMVar_ID_11728 Human_SNP_ID_595983379 A-to-I Human chr16 + 16075125 16075125 16075125 CGCTACCACACCTGGCTAATGTTTGTATTTTTAGTAGAGATGGGGTTTCACCACGTTGGCCAGGC CGCTACCACACCTGGCTAATGTTTGTATTTTTGGTAGAGATGGGGTTTCACCACGTTGGCCAGGC A G ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs902865843 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_315,RMVar_hsa_circ_279614,RMVar_hsa_circ_351085,RMVar_hsa_circ_373070,RMVar_hsa_circ_362371,RMVar_hsa_circ_88994,RMVar_hsa_circ_176596,RMVar_hsa_circ_176598,RMVar_hsa_circ_176597,RMVar_hsa_circ_176610,RMVar_hsa_circ_94441,RMVar_hsa_circ_79332,RMVar_hsa_circ_91416,RMVar_hsa_circ_176611,RMVar_hsa_circ_88330,RMVar_hsa_circ_176618,RMVar_hsa_circ_176619,RMVar_hsa_circ_15940,RMVar_hsa_circ_77185,RMVar_hsa_circ_94162,RMVar_hsa_circ_176628,RMVar_hsa_circ_176629,RMVar_hsa_circ_344358,RMVar_hsa_circ_337336,RMVar_hsa_circ_113461,RMVar_hsa_circ_122709,RMVar_hsa_circ_29310,RMVar_hsa_circ_176630,RMVar_hsa_circ_176631,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_91549,RMVar_hsa_circ_81981,RMVar_hsa_circ_34386,RMVar_hsa_circ_125055,RMVar_hsa_circ_176642,RMVar_hsa_circ_176643,RMVar_hsa_circ_316705,RMVar_hsa_circ_374663,RMVar_hsa_circ_100014,RMVar_hsa_circ_107296,RMVar_hsa_circ_176644,RMVar_hsa_circ_176646,RMVar_hsa_circ_176647,RMVar_hsa_circ_176645,RMVar_hsa_circ_106446,RMVar_hsa_circ_286548,RMVar_hsa_circ_47523,RMVar_hsa_circ_176651 11729 RMVar_ID_11729 Human_SNP_ID_595983508 A-to-I Human chr16 + 16075588 16075588 16075588 GGGAGATGGAGGTTGCAGTAGGCCGAGATCGCACCACTGCGCTCCAGCCTGGGTGCAGAAGCCAG GGGAGATGGAGGTTGCAGTAGGCCGAGATCGCGCCACTGCGCTCCAGCCTGGGTGCAGAAGCCAG A G ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934571735 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12675165 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_279614,RMVar_hsa_circ_351085,RMVar_hsa_circ_373070,RMVar_hsa_circ_362371,RMVar_hsa_circ_88994,RMVar_hsa_circ_176596,RMVar_hsa_circ_176598,RMVar_hsa_circ_176597,RMVar_hsa_circ_176610,RMVar_hsa_circ_94441,RMVar_hsa_circ_79332,RMVar_hsa_circ_91416,RMVar_hsa_circ_176611,RMVar_hsa_circ_88330,RMVar_hsa_circ_176618,RMVar_hsa_circ_176619,RMVar_hsa_circ_15940,RMVar_hsa_circ_77185,RMVar_hsa_circ_94162,RMVar_hsa_circ_176628,RMVar_hsa_circ_176629,RMVar_hsa_circ_344358,RMVar_hsa_circ_337336,RMVar_hsa_circ_113461,RMVar_hsa_circ_122709,RMVar_hsa_circ_29310,RMVar_hsa_circ_176630,RMVar_hsa_circ_176631,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_91549,RMVar_hsa_circ_81981,RMVar_hsa_circ_34386,RMVar_hsa_circ_125055,RMVar_hsa_circ_176642,RMVar_hsa_circ_176643,RMVar_hsa_circ_316705,RMVar_hsa_circ_374663,RMVar_hsa_circ_100014,RMVar_hsa_circ_107296,RMVar_hsa_circ_176644,RMVar_hsa_circ_176646,RMVar_hsa_circ_176647,RMVar_hsa_circ_176645,RMVar_hsa_circ_106446,RMVar_hsa_circ_286548,RMVar_hsa_circ_47523,RMVar_hsa_circ_176651 11730 RMVar_ID_11730 Human_SNP_ID_595985030 A-to-I Human chr16 + 16080889 16080888 16080890 ATGACGTTGTTTGTTGTTGTGGGTTTTGAGACAGAGTTTTTTTTGTTGCCCAGGCTGGAGTGCAG ATGACGTTGTTTGTTGTTGTGGGTTTTGAGAC__AGTTTTTTTTGTTGCCCAGGCTGGAGTGCAG CAG C ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973958769 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_12675179 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_279614,RMVar_hsa_circ_351085,RMVar_hsa_circ_373070,RMVar_hsa_circ_88994,RMVar_hsa_circ_176596,RMVar_hsa_circ_176598,RMVar_hsa_circ_176597,RMVar_hsa_circ_176610,RMVar_hsa_circ_94441,RMVar_hsa_circ_79332,RMVar_hsa_circ_176611,RMVar_hsa_circ_88330,RMVar_hsa_circ_176619,RMVar_hsa_circ_12043,RMVar_hsa_circ_77185,RMVar_hsa_circ_94162,RMVar_hsa_circ_176628,RMVar_hsa_circ_176629,RMVar_hsa_circ_344358,RMVar_hsa_circ_337336,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_91549,RMVar_hsa_circ_81981,RMVar_hsa_circ_125055,RMVar_hsa_circ_176642,RMVar_hsa_circ_176643,RMVar_hsa_circ_374663,RMVar_hsa_circ_100014,RMVar_hsa_circ_107296,RMVar_hsa_circ_176644,RMVar_hsa_circ_176646,RMVar_hsa_circ_176647,RMVar_hsa_circ_176645,RMVar_hsa_circ_106446,RMVar_hsa_circ_303944,RMVar_hsa_circ_47523,RMVar_hsa_circ_176651,RMVar_hsa_circ_373659,RMVar_hsa_circ_120394,RMVar_hsa_circ_127456,RMVar_hsa_circ_111689,RMVar_hsa_circ_44512,RMVar_hsa_circ_176652,RMVar_hsa_circ_176654,RMVar_hsa_circ_176656,RMVar_hsa_circ_176655,RMVar_hsa_circ_176653,RMVar_hsa_circ_97231,RMVar_hsa_circ_378402,RMVar_hsa_circ_176658,RMVar_hsa_circ_176659 11731 RMVar_ID_11731 Human_SNP_ID_595985380 A-to-I Human chr16 + 16082325 16082325 16082325 TATGTTTGAGCTGAGCATGATGGCTCATGCCTATAATCCCAGCACTTCAGGAGGCCAAGGCAGGA TATGTTTGAGCTGAGCATGATGGCTCATGCCTGTAATCCCAGCACTTCAGGAGGCCAAGGCAGGA A G ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1276297976 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_315,RMVar_hsa_circ_279614,RMVar_hsa_circ_351085,RMVar_hsa_circ_373070,RMVar_hsa_circ_88994,RMVar_hsa_circ_176596,RMVar_hsa_circ_176598,RMVar_hsa_circ_176597,RMVar_hsa_circ_176610,RMVar_hsa_circ_94441,RMVar_hsa_circ_79332,RMVar_hsa_circ_176611,RMVar_hsa_circ_88330,RMVar_hsa_circ_176619,RMVar_hsa_circ_12043,RMVar_hsa_circ_77185,RMVar_hsa_circ_94162,RMVar_hsa_circ_176628,RMVar_hsa_circ_176629,RMVar_hsa_circ_344358,RMVar_hsa_circ_337336,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_91549,RMVar_hsa_circ_81981,RMVar_hsa_circ_125055,RMVar_hsa_circ_176642,RMVar_hsa_circ_176643,RMVar_hsa_circ_374663,RMVar_hsa_circ_100014,RMVar_hsa_circ_107296,RMVar_hsa_circ_176644,RMVar_hsa_circ_176646,RMVar_hsa_circ_176647,RMVar_hsa_circ_176645,RMVar_hsa_circ_106446,RMVar_hsa_circ_303944,RMVar_hsa_circ_47523,RMVar_hsa_circ_176651,RMVar_hsa_circ_373659,RMVar_hsa_circ_120394,RMVar_hsa_circ_127456,RMVar_hsa_circ_111689,RMVar_hsa_circ_44512,RMVar_hsa_circ_176652,RMVar_hsa_circ_176654,RMVar_hsa_circ_176656,RMVar_hsa_circ_176655,RMVar_hsa_circ_176653,RMVar_hsa_circ_97231,RMVar_hsa_circ_378402,RMVar_hsa_circ_176658,RMVar_hsa_circ_176659 11732 RMVar_ID_11732 Human_SNP_ID_595985524 A-to-I Human chr16 + 16082857 16082857 16082857 TTTTTTAGAGATGGGATTTCTCTATGTTGTCCAGGCTGGCTTTGAACTCCTGACCTCAAGCAGTC TTTTTTAGAGATGGGATTTCTCTATGTTGTCCGGGCTGGCTTTGAACTCCTGACCTCAAGCAGTC A G ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs553606604 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_315,RMVar_hsa_circ_279614,RMVar_hsa_circ_351085,RMVar_hsa_circ_373070,RMVar_hsa_circ_88994,RMVar_hsa_circ_176596,RMVar_hsa_circ_176598,RMVar_hsa_circ_176597,RMVar_hsa_circ_176610,RMVar_hsa_circ_94441,RMVar_hsa_circ_79332,RMVar_hsa_circ_176611,RMVar_hsa_circ_88330,RMVar_hsa_circ_176619,RMVar_hsa_circ_12043,RMVar_hsa_circ_77185,RMVar_hsa_circ_94162,RMVar_hsa_circ_176628,RMVar_hsa_circ_176629,RMVar_hsa_circ_344358,RMVar_hsa_circ_337336,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_91549,RMVar_hsa_circ_81981,RMVar_hsa_circ_125055,RMVar_hsa_circ_176642,RMVar_hsa_circ_176643,RMVar_hsa_circ_374663,RMVar_hsa_circ_100014,RMVar_hsa_circ_107296,RMVar_hsa_circ_176644,RMVar_hsa_circ_176646,RMVar_hsa_circ_176647,RMVar_hsa_circ_176645,RMVar_hsa_circ_106446,RMVar_hsa_circ_303944,RMVar_hsa_circ_47523,RMVar_hsa_circ_176651,RMVar_hsa_circ_373659,RMVar_hsa_circ_120394,RMVar_hsa_circ_127456,RMVar_hsa_circ_111689,RMVar_hsa_circ_44512,RMVar_hsa_circ_176652,RMVar_hsa_circ_176654,RMVar_hsa_circ_176656,RMVar_hsa_circ_176655,RMVar_hsa_circ_176653,RMVar_hsa_circ_97231,RMVar_hsa_circ_378402,RMVar_hsa_circ_176658,RMVar_hsa_circ_176659 11733 RMVar_ID_11733 Human_SNP_ID_595985538 A-to-I Human chr16 + 16082908 16082908 16082908 GACCTCAAGCAGTCTGCCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGCG GACCTCAAGCAGTCTGCCTGCCTTGGCCTCCCCAAGTGCTGGGATTACAGGCATGAGCCACTGCG A C ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs186939482 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_315,RMVar_hsa_circ_279614,RMVar_hsa_circ_351085,RMVar_hsa_circ_373070,RMVar_hsa_circ_88994,RMVar_hsa_circ_176596,RMVar_hsa_circ_176598,RMVar_hsa_circ_176597,RMVar_hsa_circ_176610,RMVar_hsa_circ_94441,RMVar_hsa_circ_79332,RMVar_hsa_circ_176611,RMVar_hsa_circ_88330,RMVar_hsa_circ_176619,RMVar_hsa_circ_12043,RMVar_hsa_circ_77185,RMVar_hsa_circ_94162,RMVar_hsa_circ_176628,RMVar_hsa_circ_176629,RMVar_hsa_circ_344358,RMVar_hsa_circ_337336,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_91549,RMVar_hsa_circ_81981,RMVar_hsa_circ_125055,RMVar_hsa_circ_176642,RMVar_hsa_circ_176643,RMVar_hsa_circ_374663,RMVar_hsa_circ_100014,RMVar_hsa_circ_107296,RMVar_hsa_circ_176644,RMVar_hsa_circ_176646,RMVar_hsa_circ_176647,RMVar_hsa_circ_176645,RMVar_hsa_circ_106446,RMVar_hsa_circ_303944,RMVar_hsa_circ_47523,RMVar_hsa_circ_176651,RMVar_hsa_circ_373659,RMVar_hsa_circ_120394,RMVar_hsa_circ_127456,RMVar_hsa_circ_111689,RMVar_hsa_circ_44512,RMVar_hsa_circ_176652,RMVar_hsa_circ_176654,RMVar_hsa_circ_176656,RMVar_hsa_circ_176655,RMVar_hsa_circ_176653,RMVar_hsa_circ_97231,RMVar_hsa_circ_378402,RMVar_hsa_circ_176658,RMVar_hsa_circ_176659 11734 RMVar_ID_11734 Human_SNP_ID_595995300 A-to-I Human chr16 + 16113387 16113387 16113387 GCTGTTAAAATTAAATAAACGTTGGGCGCAGTAGCTCACGCCTGTAACCCCAACACTTTGAGAGG GCTGTTAAAATTAAATAAACGTTGGGCGCAGTGGCTCACGCCTGTAACCCCAACACTTTGAGAGG A G ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1186479699 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_176610,RMVar_hsa_circ_94441,RMVar_hsa_circ_85359,RMVar_hsa_circ_113461,RMVar_hsa_circ_29310,RMVar_hsa_circ_176630,RMVar_hsa_circ_87122,RMVar_hsa_circ_176638,RMVar_hsa_circ_81981,RMVar_hsa_circ_125055,RMVar_hsa_circ_176643,RMVar_hsa_circ_176644,RMVar_hsa_circ_120394,RMVar_hsa_circ_127456,RMVar_hsa_circ_176652,RMVar_hsa_circ_176653,RMVar_hsa_circ_268855,RMVar_hsa_circ_78564,RMVar_hsa_circ_122136,RMVar_hsa_circ_126661,RMVar_hsa_circ_176665,RMVar_hsa_circ_311696,RMVar_hsa_circ_318613,RMVar_hsa_circ_176666,RMVar_hsa_circ_176668,RMVar_hsa_circ_176667,RMVar_hsa_circ_91129,RMVar_hsa_circ_371721,RMVar_hsa_circ_118807,RMVar_hsa_circ_87320,RMVar_hsa_circ_176673,RMVar_hsa_circ_176675,RMVar_hsa_circ_176676,RMVar_hsa_circ_176674,RMVar_hsa_circ_176672 11735 RMVar_ID_11735 Human_SNP_ID_595995305 A-to-I Human chr16 + 16113406 16113404 16113407 CGTTGGGCGCAGTAGCTCACGCCTGTAACCCCAACACTTTGAGAGGCCAAGGCGGGTGGATCGCT CGTTGGGCGCAGTAGCTCACGCCTGTAACCC___CACTTTGAGAGGCCAAGGCGGGTGGATCGCT CCAA C ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1399700790 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,RMVar_hsa_circ_88994,RMVar_hsa_circ_176596,RMVar_hsa_circ_176610,RMVar_hsa_circ_94441,RMVar_hsa_circ_85359,RMVar_hsa_circ_113461,RMVar_hsa_circ_29310,RMVar_hsa_circ_176630,RMVar_hsa_circ_87122,RMVar_hsa_circ_176638,RMVar_hsa_circ_81981,RMVar_hsa_circ_125055,RMVar_hsa_circ_176643,RMVar_hsa_circ_176644,RMVar_hsa_circ_120394,RMVar_hsa_circ_127456,RMVar_hsa_circ_176652,RMVar_hsa_circ_176653,RMVar_hsa_circ_268855,RMVar_hsa_circ_78564,RMVar_hsa_circ_122136,RMVar_hsa_circ_126661,RMVar_hsa_circ_176665,RMVar_hsa_circ_311696,RMVar_hsa_circ_318613,RMVar_hsa_circ_176666,RMVar_hsa_circ_176668,RMVar_hsa_circ_176667,RMVar_hsa_circ_91129,RMVar_hsa_circ_371721,RMVar_hsa_circ_118807,RMVar_hsa_circ_87320,RMVar_hsa_circ_176673,RMVar_hsa_circ_176675,RMVar_hsa_circ_176676,RMVar_hsa_circ_176674,RMVar_hsa_circ_176672 11736 RMVar_ID_11736 Human_SNP_ID_595995346 A-to-I Human chr16 + 16113575 16113575 16113575 TACTCAGGAGGCTGAGGTGGGAGGATTGCTTGAGCCCAGGAGGTCGAGGCTGCAGTGAGCCGTGA TACTCAGGAGGCTGAGGTGGGAGGATTGCTTGGGCCCAGGAGGTCGAGGCTGCAGTGAGCCGTGA A G ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1017575005 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_176610,RMVar_hsa_circ_94441,RMVar_hsa_circ_85359,RMVar_hsa_circ_113461,RMVar_hsa_circ_29310,RMVar_hsa_circ_176630,RMVar_hsa_circ_87122,RMVar_hsa_circ_176638,RMVar_hsa_circ_81981,RMVar_hsa_circ_125055,RMVar_hsa_circ_176643,RMVar_hsa_circ_176644,RMVar_hsa_circ_120394,RMVar_hsa_circ_127456,RMVar_hsa_circ_176652,RMVar_hsa_circ_176653,RMVar_hsa_circ_268855,RMVar_hsa_circ_78564,RMVar_hsa_circ_122136,RMVar_hsa_circ_126661,RMVar_hsa_circ_176665,RMVar_hsa_circ_311696,RMVar_hsa_circ_318613,RMVar_hsa_circ_176666,RMVar_hsa_circ_176668,RMVar_hsa_circ_176667,RMVar_hsa_circ_91129,RMVar_hsa_circ_371721,RMVar_hsa_circ_118807,RMVar_hsa_circ_87320,RMVar_hsa_circ_176673,RMVar_hsa_circ_176675,RMVar_hsa_circ_176676,RMVar_hsa_circ_176674,RMVar_hsa_circ_176672 11737 RMVar_ID_11737 Human_SNP_ID_595995649 A-to-I Human chr16 + 16114538 16114538 16114538 AATTTTTGTATTTTTAGGAGAGACGGAGTTTCACTGTGTTGGCCAGGCTGGTCTCGATCTCCTGA AATTTTTGTATTTTTAGGAGAGACGGAGTTTCGCTGTGTTGGCCAGGCTGGTCTCGATCTCCTGA A G ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs770469921 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_176610,RMVar_hsa_circ_94441,RMVar_hsa_circ_85359,RMVar_hsa_circ_113461,RMVar_hsa_circ_29310,RMVar_hsa_circ_176630,RMVar_hsa_circ_87122,RMVar_hsa_circ_176638,RMVar_hsa_circ_81981,RMVar_hsa_circ_125055,RMVar_hsa_circ_176643,RMVar_hsa_circ_176644,RMVar_hsa_circ_120394,RMVar_hsa_circ_127456,RMVar_hsa_circ_176652,RMVar_hsa_circ_176653,RMVar_hsa_circ_268855,RMVar_hsa_circ_78564,RMVar_hsa_circ_122136,RMVar_hsa_circ_126661,RMVar_hsa_circ_176665,RMVar_hsa_circ_311696,RMVar_hsa_circ_318613,RMVar_hsa_circ_176666,RMVar_hsa_circ_176668,RMVar_hsa_circ_176667,RMVar_hsa_circ_91129,RMVar_hsa_circ_371721,RMVar_hsa_circ_118807,RMVar_hsa_circ_87320,RMVar_hsa_circ_176673,RMVar_hsa_circ_176675,RMVar_hsa_circ_176676,RMVar_hsa_circ_176674,RMVar_hsa_circ_176672 11738 RMVar_ID_11738 Human_SNP_ID_595995666 A-to-I Human chr16 + 16114615 16114615 16114615 CACCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCATGCCTGGTTCATCATT CACCCACCTCGGCCTCCCAAAGTGCTGGGATTGCAGGTGTGAGCCACCATGCCTGGTTCATCATT A G ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1356453760 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_176610,RMVar_hsa_circ_94441,RMVar_hsa_circ_85359,RMVar_hsa_circ_113461,RMVar_hsa_circ_29310,RMVar_hsa_circ_176630,RMVar_hsa_circ_87122,RMVar_hsa_circ_176638,RMVar_hsa_circ_81981,RMVar_hsa_circ_125055,RMVar_hsa_circ_176643,RMVar_hsa_circ_176644,RMVar_hsa_circ_120394,RMVar_hsa_circ_127456,RMVar_hsa_circ_176652,RMVar_hsa_circ_176653,RMVar_hsa_circ_268855,RMVar_hsa_circ_78564,RMVar_hsa_circ_122136,RMVar_hsa_circ_126661,RMVar_hsa_circ_176665,RMVar_hsa_circ_311696,RMVar_hsa_circ_318613,RMVar_hsa_circ_176666,RMVar_hsa_circ_176668,RMVar_hsa_circ_176667,RMVar_hsa_circ_91129,RMVar_hsa_circ_371721,RMVar_hsa_circ_118807,RMVar_hsa_circ_87320,RMVar_hsa_circ_176673,RMVar_hsa_circ_176675,RMVar_hsa_circ_176676,RMVar_hsa_circ_176674,RMVar_hsa_circ_176672 11739 RMVar_ID_11739 Human_SNP_ID_595999352 A-to-I Human chr16 + 16126477 16126477 16126477 ACAATCTCGGCTCACTGCAACCTCCTCCTCCCAGGTTCAAGTAATTCTCCTGCCTCAGCCTCCCA ACAATCTCGGCTCACTGCAACCTCCTCCTCCCGGGTTCAAGTAATTCTCCTGCCTCAGCCTCCCA A G ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs753933308 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 11740 RMVar_ID_11740 Human_SNP_ID_595999998 A-to-I Human chr16 + 16128765 16128765 16128765 CCACGCCTGCAATCCCAGCACTTTGAGAGGCCAAGGTGGGTGGATCACTTGAAGCCAGGAGTTCG CCACGCCTGCAATCCCAGCACTTTGAGAGGCCGAGGTGGGTGGATCACTTGAAGCCAGGAGTTCG A G ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1158342402 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 11741 RMVar_ID_11741 Human_SNP_ID_596000287 A-to-I Human chr16 + 16129687 16129687 16129687 AACCTCCCAAGTAGCTGAGATTACAGGCTCCCACCATCAGGCCCAGCTAATTTTTGTATTTTTAG AACCTCCCAAGTAGCTGAGATTACAGGCTCCCGCCATCAGGCCCAGCTAATTTTTGTATTTTTAG A G ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1211681686 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 11742 RMVar_ID_11742 Human_SNP_ID_596003878 A-to-I Human chr16 + 16140685 16140685 16140685 CAGGCCACAGATCTGGCCCCCTGCGTGTTTTTATGAATAAAGTTTTATTGGCACGCAGCCACATC CAGGCCACAGATCTGGCCCCCTGCGTGTTTTTGTGAATAAAGTTTTATTGGCACGCAGCCACATC A G ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1009433202 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 11743 RMVar_ID_11743 Human_SNP_ID_596003882 A-to-I Human chr16 + 16140699 16140699 16140699 GGCCCCCTGCGTGTTTTTATGAATAAAGTTTTATTGGCACGCAGCCACATCTGTTCATTTTCCTG GGCCCCCTGCGTGTTTTTATGAATAAAGTTTTTTTGGCACGCAGCCACATCTGTTCATTTTCCTG A T ABCC1 Ensembl:ENSG00000103222 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1345386268 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 11744 RMVar_ID_11744 Human_SNP_ID_596006249 A-to-I Human chr16 + 16148731 16148731 16148731 GGGAGGTGGAGGTTGCAGTGAGTCAAGATTGCACCCCTGCACTCCGGCTTGGGTGACAGAGTGAG GGGAGGTGGAGGTTGCAGTGAGTCAAGATTGCCCCCCTGCACTCCGGCTTGGGTGACAGAGTGAG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1247940741 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 11745 RMVar_ID_11745 Human_SNP_ID_596008890 A-to-I Human chr16 - 16156771 16156771 16156771 ACCCGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGCTATGAA ACCCGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGCTATGAA T C ABCC6 Ensembl:ENSG00000091262 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1035916875 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81511,RMVar_hsa_circ_110785,RMVar_hsa_circ_176688,RMVar_hsa_circ_176689 11746 RMVar_ID_11746 Human_SNP_ID_596039045 A-to-I Human chr16 - 16324932 16324932 16324932 GCTGCTCCCCCTACGCAGGCCTGCACTCACCCATGCATTCGAAGTGCACCTTGGTGGTGAGAGCG GCTGCTCCCCCTACGCAGGCCTGCACTCACCCTTGCATTCGAAGTGCACCTTGGTGGTGAGAGCG T A lnc-ABCC6-5 RNACentral:URS00009C1DDA lincRNA exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs558042008 Functional Loss SNV dbSNP153 33..33 33 - - - 11747 RMVar_ID_11747 Human_SNP_ID_596039046 A-to-I Human chr16 - 16324932 16324932 16324932 GCTGCTCCCCCTACGCAGGCCTGCACTCACCCATGCATTCGAAGTGCACCTTGGTGGTGAGAGCG GCTGCTCCCCCTACGCAGGCCTGCACTCACCCGTGCATTCGAAGTGCACCTTGGTGGTGAGAGCG T C lnc-ABCC6-5 RNACentral:URS00009C1DDA lincRNA exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs558042008 Functional Loss SNV dbSNP153 33..33 33 - - - 11748 RMVar_ID_11748 Human_SNP_ID_596039047 A-to-I Human chr16 - 16324932 16324932 16324932 GCTGCTCCCCCTACGCAGGCCTGCACTCACCCATGCATTCGAAGTGCACCTTGGTGGTGAGAGCG GCTGCTCCCCCTACGCAGGCCTGCACTCACCCCTGCATTCGAAGTGCACCTTGGTGGTGAGAGCG T G lnc-ABCC6-5 RNACentral:URS00009C1DDA lincRNA exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs558042008 Functional Loss SNV dbSNP153 33..33 33 - - - 11749 RMVar_ID_11749 Human_SNP_ID_596039986 A-to-I Human chr16 + 16329208 16329208 16329208 GCCACCTCACCGCCTTCGGCACCAGCCTCTTCATGCCCCCAAGCCATGTACGCTTTGTGTTTCCT GCCACCTCACCGCCTTCGGCACCAGCCTCTTCCTGCCCCCAAGCCATGTACGCTTTGTGTTTCCT A C AC138969.1,PKD1P1 Ensembl:ENSG00000183889,Ensembl:ENSG00000244257 Protein coding,Pseudogene exon,exon GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs3883137 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8941715,Human_RBP_ID_17673332,Human_RBP_ID_21959961 Human_Splice_Rec_1683893,Human_Splice_Rec_1683957 Human_miRNA_ID_1826406,Human_miRNA_ID_1826608 11750 RMVar_ID_11750 Human_SNP_ID_596039987 A-to-I Human chr16 + 16329208 16329208 16329208 GCCACCTCACCGCCTTCGGCACCAGCCTCTTCATGCCCCCAAGCCATGTACGCTTTGTGTTTCCT GCCACCTCACCGCCTTCGGCACCAGCCTCTTCGTGCCCCCAAGCCATGTACGCTTTGTGTTTCCT A G AC138969.1,PKD1P1 Ensembl:ENSG00000183889,Ensembl:ENSG00000244257 Protein coding,Pseudogene exon,exon GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs3883137 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8941715,Human_RBP_ID_17673332,Human_RBP_ID_21959961 Human_Splice_Rec_1683893,Human_Splice_Rec_1683957 Human_miRNA_ID_1826406,Human_miRNA_ID_1826608 11751 RMVar_ID_11751 Human_SNP_ID_596041334 A-to-I Human chr16 + 16337832 16337832 16337832 GTTGGTCCGGCTGGTTTTGAACTCCCGACCTCAGGTGATCCGCCTGCCTCGGCCTCCCAAAGTGT GTTGGTCCGGCTGGTTTTGAACTCCCGACCTCGGGTGATCCGCCTGCCTCGGCCTCCCAAAGTGT A G AC138969.1 Ensembl:ENSG00000183889 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1299969233 Functional Loss SNV dbSNP153 33..33 33 - - - 11752 RMVar_ID_11752 Human_SNP_ID_596133268 A-to-I Human chr16 + 16780355 16780355 16780355 CCTGCCTCAGCTTCCTGAGTGGCTGGGATTACAGGTGCCCGCCACCACGCCCGGCTAATTTTTTG CCTGCCTCAGCTTCCTGAGTGGCTGGGATTACGGGTGCCCGCCACCACGCCCGGCTAATTTTTTG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1234356854 Functional Loss SNV dbSNP153 33..33 33 - - - 11753 RMVar_ID_11753 Human_SNP_ID_596519222 A-to-I Human chr16 - 18324472 18324472 18324472 TCCTAGGTGTCTTTCCTGAAGACTATCTTCCCATCTCAAAATGGACATGATGGATCCACGGATGT TCCTAGGTGTCTTTCCTGAAGACTATCTTCCCGTCTCAAAATGGACATGATGGATCCACGGATGT T C NPIPA8,AC126755.7 Ensembl:ENSG00000214940,Ensembl:ENSG00000285628 Protein coding,lincRNA CDS,exon GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs750188546 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1684226,Human_Splice_Rec_1684227,Human_Splice_Rec_1684240,Human_Splice_Rec_1684241,Human_Splice_Rec_1684290,Human_Splice_Rec_1684291 11754 RMVar_ID_11754 Human_SNP_ID_596523422 A-to-I Human chr16 - 18348003 18348003 18348003 CCCTGCCTCCCTCTCCACAGGTCACCCTCCACAGCCAGGATGTCCTCATGCTCCCTGGTGACCTC CCCTGCCTCCCTCTCCACAGGTCACCCTCCACGGCCAGGATGTCCTCATGCTCCCTGGTGACCTC T C AC126755.1 Ensembl:ENSG00000205746 Pseudogene exon GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1258051131 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5690,Human_RBP_ID_760323,Human_RBP_ID_816232,Human_RBP_ID_891608,Human_RBP_ID_3510545,Human_RBP_ID_3947368,Human_RBP_ID_5088025,Human_RBP_ID_5183221,Human_RBP_ID_5524100,Human_RBP_ID_5572885,Human_RBP_ID_8188622,Human_RBP_ID_8726977,Human_RBP_ID_9257211,Human_RBP_ID_9286562,Human_RBP_ID_9421919,Human_RBP_ID_9841653,Human_RBP_ID_17079113,Human_RBP_ID_17257623,Human_RBP_ID_17372491,Human_RBP_ID_17488507,Human_RBP_ID_17565321,Human_RBP_ID_17608109,Human_RBP_ID_17884475,Human_RBP_ID_18163818,Human_RBP_ID_18486220,Human_RBP_ID_18940877,Human_RBP_ID_18983313,Human_RBP_ID_19071018,Human_RBP_ID_21973926,Human_RBP_ID_22357077,Human_RBP_ID_22370541,Human_RBP_ID_22425571,Human_RBP_ID_22541330,Human_RBP_ID_22653939,Human_RBP_ID_22738826,Human_RBP_ID_27837802 Human_Splice_Rec_1684318 RMVar_hsa_circ_83046,RMVar_hsa_circ_176753,RMVar_hsa_circ_102126,RMVar_hsa_circ_176754 11755 RMVar_ID_11755 Human_SNP_ID_596527275 A-to-I Human chr16 - 18377521 18377521 18377521 TCCAGATCGCCACCCCGCACAGCCTGGGTAGCATGTGGAAGATCCGAGTGTGGCACGACAACAAA TCCAGATCGCCACCCCGCACAGCCTGGGTAGCGTGTGGAAGATCCGAGTGTGGCACGACAACAAA T C PKD1P5,NPIPA9 Ensembl:ENSG00000254681,Ensembl:ENSG00000233024 Pseudogene,Protein coding exon,exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1406603110 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5573167 Human_Splice_Rec_1684451,Human_Splice_Rec_1684531 11756 RMVar_ID_11756 Human_SNP_ID_596527539 A-to-I Human chr16 - 18379345 18379345 18379345 CTGGGCCTGGCGGCTGTGTCTTCACAGGAGCCAACAGCGGATGTAAACTACATCGTCATGCTGAC CTGGGCCTGGCGGCTGTGTCTTCACAGGAGCCGACAGCGGATGTAAACTACATCGTCATGCTGAC T C PKD1P5 Ensembl:ENSG00000254681 Pseudogene exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs3883140 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5573168 Human_Splice_Rec_1684528 11757 RMVar_ID_11757 Human_SNP_ID_596527540 A-to-I Human chr16 - 18379345 18379345 18379345 CTGGGCCTGGCGGCTGTGTCTTCACAGGAGCCAACAGCGGATGTAAACTACATCGTCATGCTGAC CTGGGCCTGGCGGCTGTGTCTTCACAGGAGCCCACAGCGGATGTAAACTACATCGTCATGCTGAC T G PKD1P5 Ensembl:ENSG00000254681 Pseudogene exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs3883140 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5573168 Human_Splice_Rec_1684528 11758 RMVar_ID_11758 Human_SNP_ID_596588831 A-to-I Human chr16 - 18786198 18786198 18786198 ACCATGCCCGGCTAATTTTTGTATCTTTGGTAAAGACGGGGTTTCGCCATGTTGGCCAGGCTGGT ACCATGCCCGGCTAATTTTTGTATCTTTGGTAGAGACGGGGTTTCGCCATGTTGGCCAGGCTGGT T C RPS15A Ensembl:ENSG00000134419 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1309925992 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122283,RMVar_hsa_circ_176773,RMVar_hsa_circ_77194,RMVar_hsa_circ_176774,RMVar_hsa_circ_112033,RMVar_hsa_circ_176775,RMVar_hsa_circ_176777,RMVar_hsa_circ_375183 11759 RMVar_ID_11759 Human_SNP_ID_596588866 A-to-I Human chr16 - 18786302 18786302 18786302 TGGAGTGCAGTGGCACGATCTTGGCTACTGCAACCTCTGTCTCCCAGGTTCAAGCGATTCTCCTG TGGAGTGCAGTGGCACGATCTTGGCTACTGCAGCCTCTGTCTCCCAGGTTCAAGCGATTCTCCTG T C RPS15A Ensembl:ENSG00000134419 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs745525928 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_469282,Human_RBP_ID_12679198 Human_Splice_Rec_1685072,Human_Splice_Rec_1685073,Human_Splice_Rec_1685096,Human_Splice_Rec_1685097 RMVar_hsa_circ_122283,RMVar_hsa_circ_176773,RMVar_hsa_circ_77194,RMVar_hsa_circ_176774,RMVar_hsa_circ_112033,RMVar_hsa_circ_176775,RMVar_hsa_circ_176777,RMVar_hsa_circ_375183 11760 RMVar_ID_11760 Human_SNP_ID_596596471 A-to-I Human chr16 - 18813868 18813868 18813868 TGCCACCACGCCCTGCTAATTTTTGTATTTTTATAGAGACAGGATTTTGCCATGTTGGCTAGGCT TGCCACCACGCCCTGCTAATTTTTGTATTTTTGTAGAGACAGGATTTTGCCATGTTGGCTAGGCT T C SMG1 Ensembl:ENSG00000157106 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs557773096 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25194681 RMVar_hsa_circ_103304,RMVar_hsa_circ_91066,RMVar_hsa_circ_107528,RMVar_hsa_circ_117787,RMVar_hsa_circ_176786,RMVar_hsa_circ_176787,RMVar_hsa_circ_38818,RMVar_hsa_circ_176791,RMVar_hsa_circ_82048,RMVar_hsa_circ_97470,RMVar_hsa_circ_176792,RMVar_hsa_circ_176793,RMVar_hsa_circ_176790,RMVar_hsa_circ_84851,RMVar_hsa_circ_176794 11761 RMVar_ID_11761 Human_SNP_ID_596596667 A-to-I Human chr16 - 18814412 18814412 18814412 TCACTGTAACCTCCACCCCCCAGATTCAAGCAATTCTCCTGCCTCAGCTTCCTGAGTAGCTTGGA TCACTGTAACCTCCACCCCCCAGATTCAAGCAGTTCTCCTGCCTCAGCTTCCTGAGTAGCTTGGA T C SMG1 Ensembl:ENSG00000157106 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1415180243 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103304,RMVar_hsa_circ_91066,RMVar_hsa_circ_107528,RMVar_hsa_circ_117787,RMVar_hsa_circ_176786,RMVar_hsa_circ_176787,RMVar_hsa_circ_38818,RMVar_hsa_circ_176791,RMVar_hsa_circ_82048,RMVar_hsa_circ_97470,RMVar_hsa_circ_176792,RMVar_hsa_circ_176793,RMVar_hsa_circ_176790,RMVar_hsa_circ_84851,RMVar_hsa_circ_176794 11762 RMVar_ID_11762 Human_SNP_ID_596596669 A-to-I Human chr16 + 18814419 18814419 18814419 TACTCAGGAAGCTGAGGCAGGAGAATTGCTTGAATCTGGGGGGTGGAGGTTACAGTGAGCCGCAA TACTCAGGAAGCTGAGGCAGGAGAATTGCTTGTATCTGGGGGGTGGAGGTTACAGTGAGCCGCAA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs905119509 Functional Loss SNV dbSNP153 33..33 33 - - - 11763 RMVar_ID_11763 Human_SNP_ID_596597757 A-to-I Human chr16 - 18817956 18817956 18817956 TTAAGGCTACAGTGAGCCATAATTAAGCCACTATACTCCAGCCTGGGCAACAGGGGAGACCTTGT TTAAGGCTACAGTGAGCCATAATTAAGCCACTGTACTCCAGCCTGGGCAACAGGGGAGACCTTGT T C SMG1 Ensembl:ENSG00000157106 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs924334004 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3052,RMVar_hsa_circ_103304,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_176790,RMVar_hsa_circ_84851,RMVar_hsa_circ_115830,RMVar_hsa_circ_282686,RMVar_hsa_circ_330548,RMVar_hsa_circ_176794,RMVar_hsa_circ_364098,RMVar_hsa_circ_272407,RMVar_hsa_circ_72297,RMVar_hsa_circ_74302,RMVar_hsa_circ_68176,RMVar_hsa_circ_176795,RMVar_hsa_circ_176797,RMVar_hsa_circ_176799,RMVar_hsa_circ_176798,RMVar_hsa_circ_176796,RMVar_hsa_circ_69843,RMVar_hsa_circ_64506,RMVar_hsa_circ_269768,RMVar_hsa_circ_267825 11764 RMVar_ID_11764 Human_SNP_ID_596598072 A-to-I Human chr16 - 18818941 18818941 18818941 GTGGTGGTGGGTACCTGTAGTCCCAACTGCTCAGGAGTCTGAGGCAGGGGAATCGCTTGAACCTG GTGGTGGTGGGTACCTGTAGTCCCAACTGCTCGGGAGTCTGAGGCAGGGGAATCGCTTGAACCTG T C SMG1 Ensembl:ENSG00000157106 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs905393619 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3052,RMVar_hsa_circ_103304,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_176790,RMVar_hsa_circ_84851,RMVar_hsa_circ_115830,RMVar_hsa_circ_282686,RMVar_hsa_circ_330548,RMVar_hsa_circ_176794,RMVar_hsa_circ_364098,RMVar_hsa_circ_272407,RMVar_hsa_circ_72297,RMVar_hsa_circ_74302,RMVar_hsa_circ_68176,RMVar_hsa_circ_176795,RMVar_hsa_circ_176797,RMVar_hsa_circ_176799,RMVar_hsa_circ_176798,RMVar_hsa_circ_176796,RMVar_hsa_circ_69843,RMVar_hsa_circ_64506,RMVar_hsa_circ_269768,RMVar_hsa_circ_267825 11765 RMVar_ID_11765 Human_SNP_ID_596605811 A-to-I Human chr16 - 18848971 18848971 18848971 CTGCCTCCCAGGTTTAAGCAGTTCTCTGCCTCAGCTTCCCGAGTAGCTGGGATTACATGTGCGTG CTGCCTCCCAGGTTTAAGCAGTTCTCTGCCTCTGCTTCCCGAGTAGCTGGGATTACATGTGCGTG T A SMG1 Ensembl:ENSG00000157106 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1046094905 Functional Loss SNV dbSNP153 33..33 33 - - - 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_335675,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_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_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_176839,RMVar_hsa_circ_113316,RMVar_hsa_circ_87823,RMVar_hsa_circ_176845,RMVar_hsa_circ_176844,RMVar_hsa_circ_280366,RMVar_hsa_circ_116579,RMVar_hsa_circ_267701,RMVar_hsa_circ_106160,RMVar_hsa_circ_33831,RMVar_hsa_circ_176848,RMVar_hsa_circ_176849,RMVar_hsa_circ_176847,RMVar_hsa_circ_44453,RMVar_hsa_circ_372613,RMVar_hsa_circ_176850 11766 RMVar_ID_11766 Human_SNP_ID_596605812 A-to-I Human chr16 - 18848971 18848971 18848971 CTGCCTCCCAGGTTTAAGCAGTTCTCTGCCTCAGCTTCCCGAGTAGCTGGGATTACATGTGCGTG CTGCCTCCCAGGTTTAAGCAGTTCTCTGCCTCCGCTTCCCGAGTAGCTGGGATTACATGTGCGTG T G SMG1 Ensembl:ENSG00000157106 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1046094905 Functional Loss SNV dbSNP153 33..33 33 - - - 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_335675,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_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_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_176839,RMVar_hsa_circ_113316,RMVar_hsa_circ_87823,RMVar_hsa_circ_176845,RMVar_hsa_circ_176844,RMVar_hsa_circ_280366,RMVar_hsa_circ_116579,RMVar_hsa_circ_267701,RMVar_hsa_circ_106160,RMVar_hsa_circ_33831,RMVar_hsa_circ_176848,RMVar_hsa_circ_176849,RMVar_hsa_circ_176847,RMVar_hsa_circ_44453,RMVar_hsa_circ_372613,RMVar_hsa_circ_176850 11767 RMVar_ID_11767 Human_SNP_ID_596607237 A-to-I Human chr16 - 18853742 18853742 18853742 TGACACTGGCTAAATGGATCCAGGCAGAATGGAAAGAGATTTCAGGACAGCTGAAACAGGTTTAC TGACACTGGCTAAATGGATCCAGGCAGAATGGGAAGAGATTTCAGGACAGCTGAAACAGGTTTAC T C SMG1 Ensembl:ENSG00000157106 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1482462215 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1513431,Human_RBP_ID_1838926,Human_RBP_ID_4353561,Human_RBP_ID_5524184,Human_RBP_ID_12680340,Human_RBP_ID_18674216,Human_RBP_ID_23681307,Human_RBP_ID_27810939 Human_miRNA_ID_2233282 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_77120,RMVar_hsa_circ_176808,RMVar_hsa_circ_63474,RMVar_hsa_circ_105242,RMVar_hsa_circ_94673,RMVar_hsa_circ_21773,RMVar_hsa_circ_106330,RMVar_hsa_circ_176824,RMVar_hsa_circ_176825,RMVar_hsa_circ_112110,RMVar_hsa_circ_103637,RMVar_hsa_circ_176827,RMVar_hsa_circ_176828,RMVar_hsa_circ_176826,RMVar_hsa_circ_116891,RMVar_hsa_circ_322308,RMVar_hsa_circ_176834,RMVar_hsa_circ_100818,RMVar_hsa_circ_176833,RMVar_hsa_circ_28839,RMVar_hsa_circ_35676,RMVar_hsa_circ_351053,RMVar_hsa_circ_108986,RMVar_hsa_circ_176838,RMVar_hsa_circ_31934,RMVar_hsa_circ_176839,RMVar_hsa_circ_87823,RMVar_hsa_circ_106160,RMVar_hsa_circ_176848,RMVar_hsa_circ_176849,RMVar_hsa_circ_44453,RMVar_hsa_circ_372613,RMVar_hsa_circ_66002,RMVar_hsa_circ_377886,RMVar_hsa_circ_176850,RMVar_hsa_circ_48536,RMVar_hsa_circ_51478,RMVar_hsa_circ_264798,RMVar_hsa_circ_290746,RMVar_hsa_circ_42268,RMVar_hsa_circ_360774 11768 RMVar_ID_11768 Human_SNP_ID_596610998 A-to-I Human chr16 - 18867448 18867448 18867448 GCGATCTCGGCTCACTGTAACCTCTGCCTCTCAGGTTCAAGCCTCTTCTTGCCTCAGTCCCTGGG GCGATCTCGGCTCACTGTAACCTCTGCCTCTCGGGTTCAAGCCTCTTCTTGCCTCAGTCCCTGGG T C SMG1 Ensembl:ENSG00000157106 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1423377144 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117787,RMVar_hsa_circ_176793,RMVar_hsa_circ_269768,RMVar_hsa_circ_63474,RMVar_hsa_circ_94673,RMVar_hsa_circ_176825,RMVar_hsa_circ_112110,RMVar_hsa_circ_103637,RMVar_hsa_circ_176827,RMVar_hsa_circ_176826,RMVar_hsa_circ_116891,RMVar_hsa_circ_322308,RMVar_hsa_circ_176834,RMVar_hsa_circ_100818,RMVar_hsa_circ_176833,RMVar_hsa_circ_28839,RMVar_hsa_circ_35676,RMVar_hsa_circ_176838,RMVar_hsa_circ_31934,RMVar_hsa_circ_87823,RMVar_hsa_circ_176849,RMVar_hsa_circ_44453,RMVar_hsa_circ_372613,RMVar_hsa_circ_176850,RMVar_hsa_circ_48536,RMVar_hsa_circ_51478,RMVar_hsa_circ_42268,RMVar_hsa_circ_125365,RMVar_hsa_circ_6692,RMVar_hsa_circ_176857,RMVar_hsa_circ_106592,RMVar_hsa_circ_176856,RMVar_hsa_circ_265363,RMVar_hsa_circ_36483,RMVar_hsa_circ_377799,RMVar_hsa_circ_358884,RMVar_hsa_circ_61972,RMVar_hsa_circ_265326,RMVar_hsa_circ_104051,RMVar_hsa_circ_304160,RMVar_hsa_circ_3912,RMVar_hsa_circ_29871,RMVar_hsa_circ_176859 11769 RMVar_ID_11769 Human_SNP_ID_596610999 A-to-I Human chr16 - 18867448 18867448 18867448 GCGATCTCGGCTCACTGTAACCTCTGCCTCTCAGGTTCAAGCCTCTTCTTGCCTCAGTCCCTGGG GCGATCTCGGCTCACTGTAACCTCTGCCTCTCCGGTTCAAGCCTCTTCTTGCCTCAGTCCCTGGG T G SMG1 Ensembl:ENSG00000157106 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1423377144 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117787,RMVar_hsa_circ_176793,RMVar_hsa_circ_269768,RMVar_hsa_circ_63474,RMVar_hsa_circ_94673,RMVar_hsa_circ_176825,RMVar_hsa_circ_112110,RMVar_hsa_circ_103637,RMVar_hsa_circ_176827,RMVar_hsa_circ_176826,RMVar_hsa_circ_116891,RMVar_hsa_circ_322308,RMVar_hsa_circ_176834,RMVar_hsa_circ_100818,RMVar_hsa_circ_176833,RMVar_hsa_circ_28839,RMVar_hsa_circ_35676,RMVar_hsa_circ_176838,RMVar_hsa_circ_31934,RMVar_hsa_circ_87823,RMVar_hsa_circ_176849,RMVar_hsa_circ_44453,RMVar_hsa_circ_372613,RMVar_hsa_circ_176850,RMVar_hsa_circ_48536,RMVar_hsa_circ_51478,RMVar_hsa_circ_42268,RMVar_hsa_circ_125365,RMVar_hsa_circ_6692,RMVar_hsa_circ_176857,RMVar_hsa_circ_106592,RMVar_hsa_circ_176856,RMVar_hsa_circ_265363,RMVar_hsa_circ_36483,RMVar_hsa_circ_377799,RMVar_hsa_circ_358884,RMVar_hsa_circ_61972,RMVar_hsa_circ_265326,RMVar_hsa_circ_104051,RMVar_hsa_circ_304160,RMVar_hsa_circ_3912,RMVar_hsa_circ_29871,RMVar_hsa_circ_176859 11770 RMVar_ID_11770 Human_SNP_ID_596612685 A-to-I Human chr16 - 18872988 18872988 18872988 CACCATGCCCAGCTAATTTTTGTAATTTTAGTAGAGATGGGGTCCCGCTGTGTTGCCCAGGCTGG CACCATGCCCAGCTAATTTTTGTAATTTTAGTGGAGATGGGGTCCCGCTGTGTTGCCCAGGCTGG T C SMG1 Ensembl:ENSG00000157106 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1567404972 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_126939 RMVar_hsa_circ_117787,RMVar_hsa_circ_176793,RMVar_hsa_circ_94673,RMVar_hsa_circ_176825,RMVar_hsa_circ_103637,RMVar_hsa_circ_176826,RMVar_hsa_circ_31934,RMVar_hsa_circ_87823,RMVar_hsa_circ_176849,RMVar_hsa_circ_51478,RMVar_hsa_circ_42268,RMVar_hsa_circ_358884,RMVar_hsa_circ_304160,RMVar_hsa_circ_59168,RMVar_hsa_circ_3912,RMVar_hsa_circ_29871,RMVar_hsa_circ_89022,RMVar_hsa_circ_372472,RMVar_hsa_circ_176861,RMVar_hsa_circ_176862,RMVar_hsa_circ_82315,RMVar_hsa_circ_101947,RMVar_hsa_circ_176866,RMVar_hsa_circ_176867,RMVar_hsa_circ_268778,RMVar_hsa_circ_176869,RMVar_hsa_circ_102870 11771 RMVar_ID_11771 Human_SNP_ID_596612700 A-to-I Human chr16 - 18873042 18873042 18873042 TCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAAGTGTATGCCACCATGCCCA TCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTGGCTGGGATTACAAGTGTATGCCACCATGCCCA T C SMG1 Ensembl:ENSG00000157106 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1455020065 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117787,RMVar_hsa_circ_176793,RMVar_hsa_circ_94673,RMVar_hsa_circ_176825,RMVar_hsa_circ_103637,RMVar_hsa_circ_176826,RMVar_hsa_circ_31934,RMVar_hsa_circ_87823,RMVar_hsa_circ_176849,RMVar_hsa_circ_51478,RMVar_hsa_circ_42268,RMVar_hsa_circ_358884,RMVar_hsa_circ_304160,RMVar_hsa_circ_59168,RMVar_hsa_circ_3912,RMVar_hsa_circ_29871,RMVar_hsa_circ_89022,RMVar_hsa_circ_372472,RMVar_hsa_circ_176861,RMVar_hsa_circ_176862,RMVar_hsa_circ_82315,RMVar_hsa_circ_101947,RMVar_hsa_circ_176866,RMVar_hsa_circ_176867,RMVar_hsa_circ_268778,RMVar_hsa_circ_176869,RMVar_hsa_circ_102870 11772 RMVar_ID_11772 Human_SNP_ID_596612802 A-to-I Human chr16 - 18873404 18873404 18873404 CAGCCTGGCCAACATGGTGAAACTCTATCTCTACTAAAAAAATACAAAAGTTAGCAGGGCATGGT CAGCCTGGCCAACATGGTGAAACTCTATCTCTCCTAAAAAAATACAAAAGTTAGCAGGGCATGGT T G SMG1 Ensembl:ENSG00000157106 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs940475685 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117787,RMVar_hsa_circ_176793,RMVar_hsa_circ_94673,RMVar_hsa_circ_176825,RMVar_hsa_circ_103637,RMVar_hsa_circ_176826,RMVar_hsa_circ_31934,RMVar_hsa_circ_87823,RMVar_hsa_circ_176849,RMVar_hsa_circ_51478,RMVar_hsa_circ_42268,RMVar_hsa_circ_358884,RMVar_hsa_circ_304160,RMVar_hsa_circ_59168,RMVar_hsa_circ_3912,RMVar_hsa_circ_29871,RMVar_hsa_circ_89022,RMVar_hsa_circ_372472,RMVar_hsa_circ_176861,RMVar_hsa_circ_176862,RMVar_hsa_circ_82315,RMVar_hsa_circ_101947,RMVar_hsa_circ_176866,RMVar_hsa_circ_176867,RMVar_hsa_circ_268778,RMVar_hsa_circ_176869,RMVar_hsa_circ_102870 11773 RMVar_ID_11773 Human_SNP_ID_596613051 A-to-I Human chr16 - 18874204 18874204 18874204 AACCCAGGAAGTGGAGGTTGCAGTGAGCTGAGATCACACCACTGCACTCCAGTCTGGGCGACAGA AACCCAGGAAGTGGAGGTTGCAGTGAGCTGAGTTCACACCACTGCACTCCAGTCTGGGCGACAGA T A SMG1 Ensembl:ENSG00000157106 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1403697225 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25195121 RMVar_hsa_circ_117787,RMVar_hsa_circ_176793,RMVar_hsa_circ_94673,RMVar_hsa_circ_176825,RMVar_hsa_circ_103637,RMVar_hsa_circ_176826,RMVar_hsa_circ_31934,RMVar_hsa_circ_87823,RMVar_hsa_circ_176849,RMVar_hsa_circ_51478,RMVar_hsa_circ_42268,RMVar_hsa_circ_358884,RMVar_hsa_circ_304160,RMVar_hsa_circ_59168,RMVar_hsa_circ_3912,RMVar_hsa_circ_29871,RMVar_hsa_circ_89022,RMVar_hsa_circ_372472,RMVar_hsa_circ_176861,RMVar_hsa_circ_176862,RMVar_hsa_circ_82315,RMVar_hsa_circ_101947,RMVar_hsa_circ_176866,RMVar_hsa_circ_176867,RMVar_hsa_circ_268778,RMVar_hsa_circ_176869,RMVar_hsa_circ_102870 11774 RMVar_ID_11774 Human_SNP_ID_596613053 A-to-I Human chr16 - 18874231 18874231 18874231 TGGAGGCTAAGTTGGGAGAATTGCTTGAACCCAGGAAGTGGAGGTTGCAGTGAGCTGAGATCACA TGGAGGCTAAGTTGGGAGAATTGCTTGAACCCCGGAAGTGGAGGTTGCAGTGAGCTGAGATCACA T G SMG1 Ensembl:ENSG00000157106 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1250781599 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117787,RMVar_hsa_circ_176793,RMVar_hsa_circ_94673,RMVar_hsa_circ_176825,RMVar_hsa_circ_103637,RMVar_hsa_circ_176826,RMVar_hsa_circ_31934,RMVar_hsa_circ_87823,RMVar_hsa_circ_176849,RMVar_hsa_circ_51478,RMVar_hsa_circ_42268,RMVar_hsa_circ_358884,RMVar_hsa_circ_304160,RMVar_hsa_circ_59168,RMVar_hsa_circ_3912,RMVar_hsa_circ_29871,RMVar_hsa_circ_89022,RMVar_hsa_circ_372472,RMVar_hsa_circ_176861,RMVar_hsa_circ_176862,RMVar_hsa_circ_82315,RMVar_hsa_circ_101947,RMVar_hsa_circ_176866,RMVar_hsa_circ_176867,RMVar_hsa_circ_268778,RMVar_hsa_circ_176869,RMVar_hsa_circ_102870 11775 RMVar_ID_11775 Human_SNP_ID_596613059 A-to-I Human chr16 - 18874255 18874255 18874255 GCACACCTGTAATCCTAGCTACTTTGGAGGCTAAGTTGGGAGAATTGCTTGAACCCAGGAAGTGG GCACACCTGTAATCCTAGCTACTTTGGAGGCTTAGTTGGGAGAATTGCTTGAACCCAGGAAGTGG T A SMG1 Ensembl:ENSG00000157106 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1329206687 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117787,RMVar_hsa_circ_176793,RMVar_hsa_circ_94673,RMVar_hsa_circ_176825,RMVar_hsa_circ_103637,RMVar_hsa_circ_176826,RMVar_hsa_circ_31934,RMVar_hsa_circ_87823,RMVar_hsa_circ_176849,RMVar_hsa_circ_51478,RMVar_hsa_circ_42268,RMVar_hsa_circ_358884,RMVar_hsa_circ_304160,RMVar_hsa_circ_59168,RMVar_hsa_circ_3912,RMVar_hsa_circ_29871,RMVar_hsa_circ_89022,RMVar_hsa_circ_372472,RMVar_hsa_circ_176861,RMVar_hsa_circ_176862,RMVar_hsa_circ_82315,RMVar_hsa_circ_101947,RMVar_hsa_circ_176866,RMVar_hsa_circ_176867,RMVar_hsa_circ_268778,RMVar_hsa_circ_176869,RMVar_hsa_circ_102870 11776 RMVar_ID_11776 Human_SNP_ID_596613072 A-to-I Human chr16 - 18874318 18874318 18874318 CCTGGCCAACATGGTGAAACCTCGCCTCTACTAAAAATAGAAAAATTAGCCAGGGGTGGTGGTGC CCTGGCCAACATGGTGAAACCTCGCCTCTACTGAAAATAGAAAAATTAGCCAGGGGTGGTGGTGC T C SMG1 Ensembl:ENSG00000157106 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs74804533 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117787,RMVar_hsa_circ_176793,RMVar_hsa_circ_94673,RMVar_hsa_circ_176825,RMVar_hsa_circ_103637,RMVar_hsa_circ_176826,RMVar_hsa_circ_31934,RMVar_hsa_circ_87823,RMVar_hsa_circ_176849,RMVar_hsa_circ_51478,RMVar_hsa_circ_42268,RMVar_hsa_circ_358884,RMVar_hsa_circ_304160,RMVar_hsa_circ_59168,RMVar_hsa_circ_3912,RMVar_hsa_circ_29871,RMVar_hsa_circ_89022,RMVar_hsa_circ_372472,RMVar_hsa_circ_176861,RMVar_hsa_circ_176862,RMVar_hsa_circ_82315,RMVar_hsa_circ_101947,RMVar_hsa_circ_176866,RMVar_hsa_circ_176867,RMVar_hsa_circ_268778,RMVar_hsa_circ_176869,RMVar_hsa_circ_102870 11777 RMVar_ID_11777 Human_SNP_ID_596613073 A-to-I Human chr16 - 18874321 18874321 18874321 CAGCCTGGCCAACATGGTGAAACCTCGCCTCTACTAAAAATAGAAAAATTAGCCAGGGGTGGTGG CAGCCTGGCCAACATGGTGAAACCTCGCCTCTGCTAAAAATAGAAAAATTAGCCAGGGGTGGTGG T C SMG1 Ensembl:ENSG00000157106 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1455788555 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117787,RMVar_hsa_circ_176793,RMVar_hsa_circ_94673,RMVar_hsa_circ_176825,RMVar_hsa_circ_103637,RMVar_hsa_circ_176826,RMVar_hsa_circ_31934,RMVar_hsa_circ_87823,RMVar_hsa_circ_176849,RMVar_hsa_circ_51478,RMVar_hsa_circ_42268,RMVar_hsa_circ_358884,RMVar_hsa_circ_304160,RMVar_hsa_circ_59168,RMVar_hsa_circ_3912,RMVar_hsa_circ_29871,RMVar_hsa_circ_89022,RMVar_hsa_circ_372472,RMVar_hsa_circ_176861,RMVar_hsa_circ_176862,RMVar_hsa_circ_82315,RMVar_hsa_circ_101947,RMVar_hsa_circ_176866,RMVar_hsa_circ_176867,RMVar_hsa_circ_268778,RMVar_hsa_circ_176869,RMVar_hsa_circ_102870 11778 RMVar_ID_11778 Human_SNP_ID_596614703 A-to-I Human chr16 - 18879270 18879270 18879270 TCTGTACAAAAAGTCAAAAATTAGCTTGGTGTAGTGGCGTGCACCTGTAGTCCTAGCTACTCGGG TCTGTACAAAAAGTCAAAAATTAGCTTGGTGTGGTGGCGTGCACCTGTAGTCCTAGCTACTCGGG T C SMG1 Ensembl:ENSG00000157106 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1160402006 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117787,RMVar_hsa_circ_176793,RMVar_hsa_circ_103637,RMVar_hsa_circ_176826,RMVar_hsa_circ_31934,RMVar_hsa_circ_87823,RMVar_hsa_circ_176849,RMVar_hsa_circ_51478,RMVar_hsa_circ_42268,RMVar_hsa_circ_358884,RMVar_hsa_circ_304160,RMVar_hsa_circ_59168,RMVar_hsa_circ_89022,RMVar_hsa_circ_176862,RMVar_hsa_circ_82315,RMVar_hsa_circ_176867,RMVar_hsa_circ_268778,RMVar_hsa_circ_176869,RMVar_hsa_circ_102870,RMVar_hsa_circ_176870,RMVar_hsa_circ_330734,RMVar_hsa_circ_327270,RMVar_hsa_circ_265694 11779 RMVar_ID_11779 Human_SNP_ID_596619127 A-to-I Human chr16 - 18894894 18894894 18894894 AGACTGGCGTGAACCCGGGAGGTGGAGCTTGCAGTGAGCTTAGATCGCGCCACTGCACCCCAGCC AGACTGGCGTGAACCCGGGAGGTGGAGCTTGCGGTGAGCTTAGATCGCGCCACTGCACCCCAGCC T C SMG1 Ensembl:ENSG00000157106 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1257241215 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103637,RMVar_hsa_circ_176826,RMVar_hsa_circ_102771,RMVar_hsa_circ_176874,RMVar_hsa_circ_78508,RMVar_hsa_circ_51029,RMVar_hsa_circ_176875,RMVar_hsa_circ_73089,RMVar_hsa_circ_67739,RMVar_hsa_circ_52283,RMVar_hsa_circ_338973 11780 RMVar_ID_11780 Human_SNP_ID_596621555 A-to-I Human chr16 - 18904070 18904070 18904070 AGCCGGGCGTGGTGTTGGGCGCCTGTAGTTCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCG AGCCGGGCGTGGTGTTGGGCGCCTGTAGTTCCTGCTACTCGGGAGGCTGAGGCAGGAGAATGGCG T A SMG1 Ensembl:ENSG00000157106 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1330324227 Functional Loss SNV dbSNP153 33..33 33 - - - 11781 RMVar_ID_11781 Human_SNP_ID_596626428 A-to-I Human chr16 - 18920826 18920826 18920826 GCTTCCTCTCTCTTTTTCTGAAACAGAGTCTTACTCCATTGCTCAGGTTGGAGTGCAGTGGAACC GCTTCCTCTCTCTTTTTCTGAAACAGAGTCTTTCTCCATTGCTCAGGTTGGAGTGCAGTGGAACC T A SMG1 Ensembl:ENSG00000157106 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1356467610 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12680722 11782 RMVar_ID_11782 Human_SNP_ID_596626429 A-to-I Human chr16 - 18920826 18920826 18920826 GCTTCCTCTCTCTTTTTCTGAAACAGAGTCTTACTCCATTGCTCAGGTTGGAGTGCAGTGGAACC GCTTCCTCTCTCTTTTTCTGAAACAGAGTCTTGCTCCATTGCTCAGGTTGGAGTGCAGTGGAACC T C SMG1 Ensembl:ENSG00000157106 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1356467610 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12680722 11783 RMVar_ID_11783 Human_SNP_ID_596656890 A-to-I Human chr16 + 19032850 19032850 19032850 GGGGTTTCACGACGTTGGCCAGGCTGGTCTCGAACTTCTGACCTTGTGATCCACCCACCTCGGCC GGGGTTTCACGACGTTGGCCAGGCTGGTCTCGGACTTCTGACCTTGTGATCCACCCACCTCGGCC A G TMC7 Ensembl:ENSG00000170537 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1416708417 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3341,RMVar_hsa_circ_90422,RMVar_hsa_circ_12290,RMVar_hsa_circ_176880,RMVar_hsa_circ_7943,RMVar_hsa_circ_113015,RMVar_hsa_circ_176883,RMVar_hsa_circ_109328,RMVar_hsa_circ_20890,RMVar_hsa_circ_44941,RMVar_hsa_circ_176884 11784 RMVar_ID_11784 Human_SNP_ID_596664527 A-to-I Human chr16 + 19063338 19063338 19063338 ACTTTGGGAGTCCAAGGAGGGCAGATCACCTGAAGTCAGAAGTTTGAGACCAGCCTGGTCAATGT ACTTTGGGAGTCCAAGGAGGGCAGATCACCTGTAGTCAGAAGTTTGAGACCAGCCTGGTCAATGT A T TMC7 Ensembl:ENSG00000170537 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs906112762 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1100670 11785 RMVar_ID_11785 Human_SNP_ID_596664528 A-to-I Human chr16 + 19063343 19063343 19063343 GGGAGTCCAAGGAGGGCAGATCACCTGAAGTCAGAAGTTTGAGACCAGCCTGGTCAATGTGGCAA GGGAGTCCAAGGAGGGCAGATCACCTGAAGTCGGAAGTTTGAGACCAGCCTGGTCAATGTGGCAA A G TMC7 Ensembl:ENSG00000170537 Protein coding 3'UTR GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1351795184 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1100670 11786 RMVar_ID_11786 Human_SNP_ID_596665113 A-to-I Human chr16 + 19065181 19065181 19065181 GTTGGTCAGGCTGGTCTTGAACTGCTGACCTCAAGTGATCCTTCCACTTCGGCCTCCCAAAGTCT GTTGGTCAGGCTGGTCTTGAACTGCTGACCTCGAGTGATCCTTCCACTTCGGCCTCCCAAAGTCT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934038213 Functional Loss SNV dbSNP153 33..33 33 - - - 11787 RMVar_ID_11787 Human_SNP_ID_596667714 A-to-I Human chr16 + 19074264 19074264 19074264 TTTAAAAAAAAAGGCCGGGCGTGATGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGC TTTAAAAAAAAAGGCCGGGCGTGATGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGC A G COQ7 Ensembl:ENSG00000167186 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270342251 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32297,RMVar_hsa_circ_286922,RMVar_hsa_circ_10800,RMVar_hsa_circ_304525,RMVar_hsa_circ_176895 11788 RMVar_ID_11788 Human_SNP_ID_596669066 A-to-I Human chr16 + 19078713 19078713 19078713 GGGCTCAGTGATCCTCCCGTTTCGACTTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACTTCAC GGGCTCAGTGATCCTCCCGTTTCGACTTCCCAGAGTGCTGGGATTACAGGTGTGAGCCACTTCAC A G COQ7 Ensembl:ENSG00000167186 Protein coding 3'UTR GSE100210;GSE107867;GSE107867 HepG2 cell line;ASD brains,cerebellum;ASD brains,temporal_cortex - 29129909,30559470,30559470 RNA-Seq:(High) rs1278095816 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17872599 RMVar_hsa_circ_92355,RMVar_hsa_circ_176896 11789 RMVar_ID_11789 Human_SNP_ID_596677529 A-to-I Human chr16 - 19113010 19113009 19113010 TGGTTCACCCCTGTAATCCCAGCACTTTGGGAAGCCGAGGCGGCGAGAAGATCGCTTGAGTGAGG TGGTTCACCCCTGTAATCCCAGCACTTTGGGA_GCCGAGGCGGCGAGAAGATCGCTTGAGTGAGG CT C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054465206 Functional Loss DEL dbSNP153 33..33 33 - - - 11790 RMVar_ID_11790 Human_SNP_ID_596677696 A-to-I Human chr16 - 19113430 19113422 19113430 GAGAGGCCGAAGTGGGCGGATCATTTAAGGTCAGTAGTTCGAGACTAGCCTGGCCAACATGGTGA GAGAGGCCGAAGTGGGCGGATCATTTAAGGTC________GAGACTAGCCTGGCCAACATGGTGA CGAACTACT C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285237496 Functional Loss DEL dbSNP153 33..40 33 - - - 11791 RMVar_ID_11791 Human_SNP_ID_596677702 A-to-I Human chr16 - 19113430 19113430 19113430 GAGAGGCCGAAGTGGGCGGATCATTTAAGGTCAGTAGTTCGAGACTAGCCTGGCCAACATGGTGA GAGAGGCCGAAGTGGGCGGATCATTTAAGGTCGGTAGTTCGAGACTAGCCTGGCCAACATGGTGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1365186495 Functional Loss SNV dbSNP153 33..33 33 - - - 11792 RMVar_ID_11792 Human_SNP_ID_596679660 A-to-I Human chr16 + 19120105 19120105 19120105 GAACACAGGTTTTTGTTTTTGTTTTTTGAGACAGGGTCTCAGTCTGTTGCCCAGGCTGGAGTGCA GAACACAGGTTTTTGTTTTTGTTTTTTGAGACGGGGTCTCAGTCTGTTGCCCAGGCTGGAGTGCA A G ITPRIPL2,AC099518.3 Ensembl:ENSG00000205730,Ensembl:ENSG00000261427 Protein coding,lincRNA 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1033019454 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117690,RMVar_hsa_circ_82653,RMVar_hsa_circ_176897,RMVar_hsa_circ_176898 11793 RMVar_ID_11793 Human_SNP_ID_596679661 A-to-I Human chr16 + 19120113 19120113 19120113 GTTTTTGTTTTTGTTTTTTGAGACAGGGTCTCAGTCTGTTGCCCAGGCTGGAGTGCAGTGGCAAG GTTTTTGTTTTTGTTTTTTGAGACAGGGTCTCGGTCTGTTGCCCAGGCTGGAGTGCAGTGGCAAG A G ITPRIPL2,AC099518.3 Ensembl:ENSG00000205730,Ensembl:ENSG00000261427 Protein coding,lincRNA 3'UTR,exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs57236534 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1685800 RMVar_hsa_circ_117690,RMVar_hsa_circ_82653,RMVar_hsa_circ_176897,RMVar_hsa_circ_176898 11794 RMVar_ID_11794 Human_SNP_ID_596679662 A-to-I Human chr16 + 19120113 19120113 19120113 GTTTTTGTTTTTGTTTTTTGAGACAGGGTCTCAGTCTGTTGCCCAGGCTGGAGTGCAGTGGCAAG GTTTTTGTTTTTGTTTTTTGAGACAGGGTCTCTGTCTGTTGCCCAGGCTGGAGTGCAGTGGCAAG A T ITPRIPL2,AC099518.3 Ensembl:ENSG00000205730,Ensembl:ENSG00000261427 Protein coding,lincRNA 3'UTR,exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs57236534 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1685800 RMVar_hsa_circ_117690,RMVar_hsa_circ_82653,RMVar_hsa_circ_176897,RMVar_hsa_circ_176898 11795 RMVar_ID_11795 Human_SNP_ID_596679709 A-to-I Human chr16 + 19120282 19120282 19120282 TTTTAAATTATTTGTAGAGTCAGGGTCTCCCTATGTTGCCCAGGCTGGTCTTGAACTACTGGACT TTTTAAATTATTTGTAGAGTCAGGGTCTCCCTGTGTTGCCCAGGCTGGTCTTGAACTACTGGACT A G ITPRIPL2,AC099518.3 Ensembl:ENSG00000205730,Ensembl:ENSG00000261427 Protein coding,lincRNA 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934660915 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12681168 Human_miRNA_ID_1141101,Human_miRNA_ID_1369709 RMVar_hsa_circ_117690,RMVar_hsa_circ_82653,RMVar_hsa_circ_176897,RMVar_hsa_circ_176898 11796 RMVar_ID_11796 Human_SNP_ID_596679714 A-to-I Human chr16 + 19120316 19120316 19120316 GTTGCCCAGGCTGGTCTTGAACTACTGGACTCAAGCCATCCTCCCACCTCGGCCTCCCAAAGTGT GTTGCCCAGGCTGGTCTTGAACTACTGGACTCGAGCCATCCTCCCACCTCGGCCTCCCAAAGTGT A G ITPRIPL2,AC099518.3 Ensembl:ENSG00000205730,Ensembl:ENSG00000261427 Protein coding,lincRNA 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1203621706 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12681170 Human_miRNA_ID_257557,Human_miRNA_ID_261353,Human_miRNA_ID_2043567,Human_miRNA_ID_2043568,Human_miRNA_ID_2045718,Human_miRNA_ID_2045719,Human_miRNA_ID_2467153,Human_miRNA_ID_2467154 RMVar_hsa_circ_117690,RMVar_hsa_circ_82653,RMVar_hsa_circ_176897,RMVar_hsa_circ_176898 11797 RMVar_ID_11797 Human_SNP_ID_596679727 A-to-I Human chr16 + 19120356 19120356 19120356 CTCCCACCTCGGCCTCCCAAAGTGTTGGGATTATAGGCGCGAGCCACCACACCTGGCCTAAAAGC CTCCCACCTCGGCCTCCCAAAGTGTTGGGATTGTAGGCGCGAGCCACCACACCTGGCCTAAAAGC A G ITPRIPL2,AC099518.3 Ensembl:ENSG00000205730,Ensembl:ENSG00000261427 Protein coding,lincRNA 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1177138655 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6497467 Human_miRNA_ID_1117447,Human_miRNA_ID_1124622 RMVar_hsa_circ_117690,RMVar_hsa_circ_82653,RMVar_hsa_circ_176897,RMVar_hsa_circ_176898 11798 RMVar_ID_11798 Human_SNP_ID_596681302 A-to-I Human chr16 + 19126116 19126116 19126116 TAGCTCACTGCAGATTCAAACTCATGGGCTCAAAAGATCCTCCCACCTTAGCTTCCCAAGTAGCT TAGCTCACTGCAGATTCAAACTCATGGGCTCAGAAGATCCTCCCACCTTAGCTTCCCAAGTAGCT A G AC099518.3 Ensembl:ENSG00000261427 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569365180 Functional Loss SNV dbSNP153 33..33 33 - - - 11799 RMVar_ID_11799 Human_SNP_ID_596697151 A-to-I Human chr16 + 19191817 19191817 19191817 GTTTTGTTTTTTTGTTTTTGAGACTGTGTCTCACTTTGTCGCCAGACTGGAGTGTAGTGGCATGA GTTTTGTTTTTTTGTTTTTGAGACTGTGTCTCGCTTTGTCGCCAGACTGGAGTGTAGTGGCATGA A G SYT17 Ensembl:ENSG00000103528 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1217380926 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36657 11800 RMVar_ID_11800 Human_SNP_ID_596709289 A-to-I Human chr16 + 19243561 19243561 19243561 GCTGGGCGCAGTGGCTCATGCCTATAAATCCCAGCACTTTGGGAGGCTGAGGCTGGCGGATCACC GCTGGGCGCAGTGGCTCATGCCTATAAATCCCGGCACTTTGGGAGGCTGAGGCTGGCGGATCACC A G SYT17 Ensembl:ENSG00000103528 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs966256529 Functional Loss SNV dbSNP153 33..33 33 - - - 11801 RMVar_ID_11801 Human_SNP_ID_596762751 A-to-I Human chr16 + 19457381 19457369 19457382 GCACCACTGCAACCCAGCCTGGGTGACAGAGTAAGATCCTGTCTCTAAAAGAAGGACATTGAGTA GCACCACTGCAACCCAGCCTG_____________GATCCTGTCTCTAAAAGAAGGACATTGAGTA GGGTGACAGAGTAA G TMC5 Ensembl:ENSG00000103534 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1466011084 Functional Loss DEL dbSNP153 22..34 33 - - - RMVar_hsa_circ_61585 11802 RMVar_ID_11802 Human_SNP_ID_596774904 A-to-I Human chr16 - 19502573 19502573 19502573 GGAGGATTACTTGAGGCCAGACTGGGCAATATAGCAAGACCCCATCTCTAAAAAATTAGGCATGG GGAGGATTACTTGAGGCCAGACTGGGCAATATGGCAAGACCCCATCTCTAAAAAATTAGGCATGG T C GDE1 Ensembl:ENSG00000006007 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs3179016 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8428866 11803 RMVar_ID_11803 Human_SNP_ID_596786615 A-to-I Human chr16 - 19553676 19553676 19553676 GCTGCAGTGCAGTGGCACAATCTCGGCTCACTATAGCCTCCCCATCCCAGGCTCAGGCGATTCTC GCTGCAGTGCAGTGGCACAATCTCGGCTCACTGTAGCCTCCCCATCCCAGGCTCAGGCGATTCTC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs994020496 Functional Loss SNV dbSNP153 33..33 33 - - - 11804 RMVar_ID_11804 Human_SNP_ID_596787833 A-to-I Human chr16 + 19557912 19557912 19557912 CGTCTCCACAAAAATACAAAAAGTAGCCAGGCATGACGGCAGGTTCCTGTAATCCCAGCTACTTA CGTCTCCACAAAAATACAAAAAGTAGCCAGGCGTGACGGCAGGTTCCTGTAATCCCAGCTACTTA A G VPS35L Ensembl:ENSG00000103544 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs868508345 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112644,RMVar_hsa_circ_176906 11805 RMVar_ID_11805 Human_SNP_ID_596801717 A-to-I Human chr16 + 19612285 19612285 19612285 TGTTTTGTTTTGTTTTTTTGCACCAGAGTCTCACTCTGTTGCCCAGGCTGGAGTGCAGTGGTGCA TGTTTTGTTTTGTTTTTTTGCACCAGAGTCTCTCTCTGTTGCCCAGGCTGGAGTGCAGTGGTGCA A T VPS35L Ensembl:ENSG00000103544 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1309556913 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1767,RMVar_hsa_circ_78933,RMVar_hsa_circ_87390,RMVar_hsa_circ_176908,RMVar_hsa_circ_104066,RMVar_hsa_circ_78661,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_332184,RMVar_hsa_circ_119321,RMVar_hsa_circ_346390,RMVar_hsa_circ_176916,RMVar_hsa_circ_100481,RMVar_hsa_circ_176918,RMVar_hsa_circ_356335,RMVar_hsa_circ_293718,RMVar_hsa_circ_176921,RMVar_hsa_circ_176920,RMVar_hsa_circ_176922,RMVar_hsa_circ_354421,RMVar_hsa_circ_371781,RMVar_hsa_circ_363561,RMVar_hsa_circ_290787,RMVar_hsa_circ_318453,RMVar_hsa_circ_337691,RMVar_hsa_circ_4544,RMVar_hsa_circ_104887,RMVar_hsa_circ_10393,RMVar_hsa_circ_41940,RMVar_hsa_circ_176923,RMVar_hsa_circ_176924,RMVar_hsa_circ_85709,RMVar_hsa_circ_369450,RMVar_hsa_circ_34832,RMVar_hsa_circ_176925,RMVar_hsa_circ_176926,RMVar_hsa_circ_176927 11806 RMVar_ID_11806 Human_SNP_ID_596801952 A-to-I Human chr16 + 19613290 19613290 19613290 GCGCCACTGCACTCCAGCCTGGGTGACAGAGCAAGACTGCCTCAAACAAACAAACAAAAAGAGAC GCGCCACTGCACTCCAGCCTGGGTGACAGAGCGAGACTGCCTCAAACAAACAAACAAAAAGAGAC A G VPS35L Ensembl:ENSG00000103544 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs752229640 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1767,RMVar_hsa_circ_78933,RMVar_hsa_circ_87390,RMVar_hsa_circ_176908,RMVar_hsa_circ_104066,RMVar_hsa_circ_78661,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_332184,RMVar_hsa_circ_119321,RMVar_hsa_circ_346390,RMVar_hsa_circ_176916,RMVar_hsa_circ_100481,RMVar_hsa_circ_176918,RMVar_hsa_circ_356335,RMVar_hsa_circ_293718,RMVar_hsa_circ_176921,RMVar_hsa_circ_176920,RMVar_hsa_circ_176922,RMVar_hsa_circ_354421,RMVar_hsa_circ_371781,RMVar_hsa_circ_363561,RMVar_hsa_circ_290787,RMVar_hsa_circ_318453,RMVar_hsa_circ_337691,RMVar_hsa_circ_4544,RMVar_hsa_circ_104887,RMVar_hsa_circ_10393,RMVar_hsa_circ_41940,RMVar_hsa_circ_176923,RMVar_hsa_circ_176924,RMVar_hsa_circ_85709,RMVar_hsa_circ_369450,RMVar_hsa_circ_34832,RMVar_hsa_circ_176925,RMVar_hsa_circ_176926,RMVar_hsa_circ_176927 11807 RMVar_ID_11807 Human_SNP_ID_596802224 A-to-I Human chr16 + 19614485 19614485 19614485 CCAGGCTGGAGTGCAGTGGCACAATCTTGCTCACTGCAACCACCACCTCCCGGGTTCAAGCGATC CCAGGCTGGAGTGCAGTGGCACAATCTTGCTCCCTGCAACCACCACCTCCCGGGTTCAAGCGATC A C VPS35L Ensembl:ENSG00000103544 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs985860607 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1767,RMVar_hsa_circ_78933,RMVar_hsa_circ_87390,RMVar_hsa_circ_176908,RMVar_hsa_circ_104066,RMVar_hsa_circ_78661,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_332184,RMVar_hsa_circ_119321,RMVar_hsa_circ_346390,RMVar_hsa_circ_176916,RMVar_hsa_circ_100481,RMVar_hsa_circ_176918,RMVar_hsa_circ_356335,RMVar_hsa_circ_293718,RMVar_hsa_circ_176921,RMVar_hsa_circ_176920,RMVar_hsa_circ_176922,RMVar_hsa_circ_354421,RMVar_hsa_circ_371781,RMVar_hsa_circ_363561,RMVar_hsa_circ_290787,RMVar_hsa_circ_318453,RMVar_hsa_circ_337691,RMVar_hsa_circ_4544,RMVar_hsa_circ_104887,RMVar_hsa_circ_10393,RMVar_hsa_circ_41940,RMVar_hsa_circ_176923,RMVar_hsa_circ_176924,RMVar_hsa_circ_85709,RMVar_hsa_circ_369450,RMVar_hsa_circ_34832,RMVar_hsa_circ_176925,RMVar_hsa_circ_176926,RMVar_hsa_circ_176927 11808 RMVar_ID_11808 Human_SNP_ID_596802238 A-to-I Human chr16 + 19614536 19614536 19614536 GGGTTCAAGCGATCCTCCCACCTCAACCTCCCAGGTAGCTGGGTCTACAGGCGTGCGCCACCACA GGGTTCAAGCGATCCTCCCACCTCAACCTCCCCGGTAGCTGGGTCTACAGGCGTGCGCCACCACA A C VPS35L Ensembl:ENSG00000103544 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1445208984 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1767,RMVar_hsa_circ_78933,RMVar_hsa_circ_87390,RMVar_hsa_circ_176908,RMVar_hsa_circ_104066,RMVar_hsa_circ_78661,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_332184,RMVar_hsa_circ_119321,RMVar_hsa_circ_346390,RMVar_hsa_circ_176916,RMVar_hsa_circ_100481,RMVar_hsa_circ_176918,RMVar_hsa_circ_356335,RMVar_hsa_circ_293718,RMVar_hsa_circ_176921,RMVar_hsa_circ_176920,RMVar_hsa_circ_176922,RMVar_hsa_circ_354421,RMVar_hsa_circ_371781,RMVar_hsa_circ_363561,RMVar_hsa_circ_290787,RMVar_hsa_circ_318453,RMVar_hsa_circ_337691,RMVar_hsa_circ_4544,RMVar_hsa_circ_104887,RMVar_hsa_circ_10393,RMVar_hsa_circ_41940,RMVar_hsa_circ_176923,RMVar_hsa_circ_176924,RMVar_hsa_circ_85709,RMVar_hsa_circ_369450,RMVar_hsa_circ_34832,RMVar_hsa_circ_176925,RMVar_hsa_circ_176926,RMVar_hsa_circ_176927 11809 RMVar_ID_11809 Human_SNP_ID_596802277 A-to-I Human chr16 + 19614672 19614672 19614672 ACCTCAAGTGATTGGCCCACCTGGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACTGCAG ACCTCAAGTGATTGGCCCACCTGGGCCTCCCAGAGTGCTGGGATTACAGGTGTGAGCCACTGCAG A G VPS35L Ensembl:ENSG00000103544 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs57934424 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1767,RMVar_hsa_circ_78933,RMVar_hsa_circ_87390,RMVar_hsa_circ_176908,RMVar_hsa_circ_104066,RMVar_hsa_circ_78661,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_332184,RMVar_hsa_circ_119321,RMVar_hsa_circ_346390,RMVar_hsa_circ_176916,RMVar_hsa_circ_100481,RMVar_hsa_circ_176918,RMVar_hsa_circ_356335,RMVar_hsa_circ_293718,RMVar_hsa_circ_176921,RMVar_hsa_circ_176920,RMVar_hsa_circ_176922,RMVar_hsa_circ_354421,RMVar_hsa_circ_371781,RMVar_hsa_circ_363561,RMVar_hsa_circ_290787,RMVar_hsa_circ_318453,RMVar_hsa_circ_337691,RMVar_hsa_circ_4544,RMVar_hsa_circ_104887,RMVar_hsa_circ_10393,RMVar_hsa_circ_41940,RMVar_hsa_circ_176923,RMVar_hsa_circ_176924,RMVar_hsa_circ_85709,RMVar_hsa_circ_369450,RMVar_hsa_circ_34832,RMVar_hsa_circ_176925,RMVar_hsa_circ_176926,RMVar_hsa_circ_176927 11810 RMVar_ID_11810 Human_SNP_ID_596802523 A-to-I Human chr16 + 19615757 19615757 19615757 TTGAGAGGCCAGGGTGGGCAGATCATGAGGTCAGAAGATCAAGACCATCCTGGCCAATGTGGTGA TTGAGAGGCCAGGGTGGGCAGATCATGAGGTCGGAAGATCAAGACCATCCTGGCCAATGTGGTGA A G VPS35L Ensembl:ENSG00000103544 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1370504821 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1767,RMVar_hsa_circ_78933,RMVar_hsa_circ_87390,RMVar_hsa_circ_176908,RMVar_hsa_circ_104066,RMVar_hsa_circ_78661,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_332184,RMVar_hsa_circ_119321,RMVar_hsa_circ_346390,RMVar_hsa_circ_176916,RMVar_hsa_circ_100481,RMVar_hsa_circ_176918,RMVar_hsa_circ_356335,RMVar_hsa_circ_293718,RMVar_hsa_circ_176921,RMVar_hsa_circ_176920,RMVar_hsa_circ_176922,RMVar_hsa_circ_354421,RMVar_hsa_circ_371781,RMVar_hsa_circ_363561,RMVar_hsa_circ_290787,RMVar_hsa_circ_318453,RMVar_hsa_circ_337691,RMVar_hsa_circ_4544,RMVar_hsa_circ_104887,RMVar_hsa_circ_10393,RMVar_hsa_circ_41940,RMVar_hsa_circ_176923,RMVar_hsa_circ_176924,RMVar_hsa_circ_85709,RMVar_hsa_circ_369450,RMVar_hsa_circ_34832,RMVar_hsa_circ_176925,RMVar_hsa_circ_176926,RMVar_hsa_circ_176927 11811 RMVar_ID_11811 Human_SNP_ID_596802975 A-to-I Human chr16 + 19617204 19617204 19617204 ATAGCAAAACTCCATCTCTACAAAAAAATAGAAAAAATTAGCCAGACACGGTGATATATGCCTAT ATAGCAAAACTCCATCTCTACAAAAAAATAGACAAAATTAGCCAGACACGGTGATATATGCCTAT A C VPS35L Ensembl:ENSG00000103544 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs926444511 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1767,RMVar_hsa_circ_78933,RMVar_hsa_circ_87390,RMVar_hsa_circ_176908,RMVar_hsa_circ_104066,RMVar_hsa_circ_78661,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_119321,RMVar_hsa_circ_346390,RMVar_hsa_circ_176916,RMVar_hsa_circ_100481,RMVar_hsa_circ_176918,RMVar_hsa_circ_356335,RMVar_hsa_circ_176921,RMVar_hsa_circ_176922,RMVar_hsa_circ_371781,RMVar_hsa_circ_363561,RMVar_hsa_circ_337691,RMVar_hsa_circ_4544,RMVar_hsa_circ_104887,RMVar_hsa_circ_89821,RMVar_hsa_circ_284533,RMVar_hsa_circ_10393,RMVar_hsa_circ_41940,RMVar_hsa_circ_176923,RMVar_hsa_circ_85709,RMVar_hsa_circ_369450,RMVar_hsa_circ_34832,RMVar_hsa_circ_287757,RMVar_hsa_circ_330077,RMVar_hsa_circ_176925,RMVar_hsa_circ_176926,RMVar_hsa_circ_348907,RMVar_hsa_circ_306858,RMVar_hsa_circ_321547,RMVar_hsa_circ_288103,RMVar_hsa_circ_287430,RMVar_hsa_circ_287461,RMVar_hsa_circ_286552,RMVar_hsa_circ_274907,RMVar_hsa_circ_278261,RMVar_hsa_circ_281566,RMVar_hsa_circ_124672,RMVar_hsa_circ_273723,RMVar_hsa_circ_176932,RMVar_hsa_circ_176936,RMVar_hsa_circ_176940,RMVar_hsa_circ_176942,RMVar_hsa_circ_176941,RMVar_hsa_circ_176938,RMVar_hsa_circ_176939,RMVar_hsa_circ_176937,RMVar_hsa_circ_176934,RMVar_hsa_circ_176935,RMVar_hsa_circ_176933,RMVar_hsa_circ_176928,RMVar_hsa_circ_176930,RMVar_hsa_circ_176931,RMVar_hsa_circ_176929,RMVar_hsa_circ_176945,RMVar_hsa_circ_88223 11812 RMVar_ID_11812 Human_SNP_ID_596802984 A-to-I Human chr16 + 19617229 19617229 19617229 AAATAGAAAAAATTAGCCAGACACGGTGATATATGCCTATAGTCCCAGCTACTCAGGAGGCTGAG AAATAGAAAAAATTAGCCAGACACGGTGATATGTGCCTATAGTCCCAGCTACTCAGGAGGCTGAG A G VPS35L Ensembl:ENSG00000103544 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1298085319 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1767,RMVar_hsa_circ_78933,RMVar_hsa_circ_87390,RMVar_hsa_circ_176908,RMVar_hsa_circ_104066,RMVar_hsa_circ_78661,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_119321,RMVar_hsa_circ_346390,RMVar_hsa_circ_176916,RMVar_hsa_circ_100481,RMVar_hsa_circ_176918,RMVar_hsa_circ_356335,RMVar_hsa_circ_176921,RMVar_hsa_circ_176922,RMVar_hsa_circ_371781,RMVar_hsa_circ_363561,RMVar_hsa_circ_337691,RMVar_hsa_circ_4544,RMVar_hsa_circ_104887,RMVar_hsa_circ_89821,RMVar_hsa_circ_284533,RMVar_hsa_circ_10393,RMVar_hsa_circ_41940,RMVar_hsa_circ_176923,RMVar_hsa_circ_85709,RMVar_hsa_circ_369450,RMVar_hsa_circ_34832,RMVar_hsa_circ_287757,RMVar_hsa_circ_330077,RMVar_hsa_circ_176925,RMVar_hsa_circ_176926,RMVar_hsa_circ_348907,RMVar_hsa_circ_306858,RMVar_hsa_circ_321547,RMVar_hsa_circ_288103,RMVar_hsa_circ_287430,RMVar_hsa_circ_287461,RMVar_hsa_circ_286552,RMVar_hsa_circ_274907,RMVar_hsa_circ_278261,RMVar_hsa_circ_281566,RMVar_hsa_circ_124672,RMVar_hsa_circ_273723,RMVar_hsa_circ_176932,RMVar_hsa_circ_176936,RMVar_hsa_circ_176940,RMVar_hsa_circ_176942,RMVar_hsa_circ_176941,RMVar_hsa_circ_176938,RMVar_hsa_circ_176939,RMVar_hsa_circ_176937,RMVar_hsa_circ_176934,RMVar_hsa_circ_176935,RMVar_hsa_circ_176933,RMVar_hsa_circ_176928,RMVar_hsa_circ_176930,RMVar_hsa_circ_176931,RMVar_hsa_circ_176929,RMVar_hsa_circ_176945,RMVar_hsa_circ_88223 11813 RMVar_ID_11813 Human_SNP_ID_596802986 A-to-I Human chr16 + 19617235 19617235 19617235 AAAAAATTAGCCAGACACGGTGATATATGCCTATAGTCCCAGCTACTCAGGAGGCTGAGGTGGGA AAAAAATTAGCCAGACACGGTGATATATGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGTGGGA A G VPS35L Ensembl:ENSG00000103544 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1380495733 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1767,RMVar_hsa_circ_78933,RMVar_hsa_circ_87390,RMVar_hsa_circ_176908,RMVar_hsa_circ_104066,RMVar_hsa_circ_78661,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_119321,RMVar_hsa_circ_346390,RMVar_hsa_circ_176916,RMVar_hsa_circ_100481,RMVar_hsa_circ_176918,RMVar_hsa_circ_356335,RMVar_hsa_circ_176921,RMVar_hsa_circ_176922,RMVar_hsa_circ_371781,RMVar_hsa_circ_363561,RMVar_hsa_circ_337691,RMVar_hsa_circ_4544,RMVar_hsa_circ_104887,RMVar_hsa_circ_89821,RMVar_hsa_circ_284533,RMVar_hsa_circ_10393,RMVar_hsa_circ_41940,RMVar_hsa_circ_176923,RMVar_hsa_circ_85709,RMVar_hsa_circ_369450,RMVar_hsa_circ_34832,RMVar_hsa_circ_287757,RMVar_hsa_circ_330077,RMVar_hsa_circ_176925,RMVar_hsa_circ_176926,RMVar_hsa_circ_348907,RMVar_hsa_circ_306858,RMVar_hsa_circ_321547,RMVar_hsa_circ_288103,RMVar_hsa_circ_287430,RMVar_hsa_circ_287461,RMVar_hsa_circ_286552,RMVar_hsa_circ_274907,RMVar_hsa_circ_278261,RMVar_hsa_circ_281566,RMVar_hsa_circ_124672,RMVar_hsa_circ_273723,RMVar_hsa_circ_176932,RMVar_hsa_circ_176936,RMVar_hsa_circ_176940,RMVar_hsa_circ_176942,RMVar_hsa_circ_176941,RMVar_hsa_circ_176938,RMVar_hsa_circ_176939,RMVar_hsa_circ_176937,RMVar_hsa_circ_176934,RMVar_hsa_circ_176935,RMVar_hsa_circ_176933,RMVar_hsa_circ_176928,RMVar_hsa_circ_176930,RMVar_hsa_circ_176931,RMVar_hsa_circ_176929,RMVar_hsa_circ_176945,RMVar_hsa_circ_88223 11814 RMVar_ID_11814 Human_SNP_ID_596807232 A-to-I Human chr16 + 19634314 19634314 19634314 TAAAAATTAGCCATGCGTGGTGGTGCATGCCTATAGTCCCAGCTACCTGGGATGCTATAGTAGGA TAAAAATTAGCCATGCGTGGTGGTGCATGCCTGTAGTCCCAGCTACCTGGGATGCTATAGTAGGA A G VPS35L Ensembl:ENSG00000103544 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs907063176 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87390,RMVar_hsa_circ_176911,RMVar_hsa_circ_377326,RMVar_hsa_circ_176922,RMVar_hsa_circ_371781,RMVar_hsa_circ_363561,RMVar_hsa_circ_4544,RMVar_hsa_circ_104887,RMVar_hsa_circ_89821,RMVar_hsa_circ_284533,RMVar_hsa_circ_10393,RMVar_hsa_circ_41940,RMVar_hsa_circ_176923,RMVar_hsa_circ_85709,RMVar_hsa_circ_369450,RMVar_hsa_circ_34832,RMVar_hsa_circ_287757,RMVar_hsa_circ_176925,RMVar_hsa_circ_176926,RMVar_hsa_circ_348907,RMVar_hsa_circ_288103,RMVar_hsa_circ_287430,RMVar_hsa_circ_287461,RMVar_hsa_circ_274907,RMVar_hsa_circ_281566,RMVar_hsa_circ_124672,RMVar_hsa_circ_273723,RMVar_hsa_circ_176932,RMVar_hsa_circ_176936,RMVar_hsa_circ_176937,RMVar_hsa_circ_176934,RMVar_hsa_circ_176935,RMVar_hsa_circ_176933,RMVar_hsa_circ_176928,RMVar_hsa_circ_176930,RMVar_hsa_circ_176931,RMVar_hsa_circ_176929,RMVar_hsa_circ_68916,RMVar_hsa_circ_373099,RMVar_hsa_circ_54963,RMVar_hsa_circ_18908,RMVar_hsa_circ_30805,RMVar_hsa_circ_16385,RMVar_hsa_circ_321996,RMVar_hsa_circ_176946,RMVar_hsa_circ_176947,RMVar_hsa_circ_332208,RMVar_hsa_circ_344504,RMVar_hsa_circ_329966,RMVar_hsa_circ_16422,RMVar_hsa_circ_176950,RMVar_hsa_circ_176951,RMVar_hsa_circ_176949,RMVar_hsa_circ_176954,RMVar_hsa_circ_25052,RMVar_hsa_circ_298390,RMVar_hsa_circ_334287,RMVar_hsa_circ_337162,RMVar_hsa_circ_300765,RMVar_hsa_circ_278485,RMVar_hsa_circ_296139,RMVar_hsa_circ_71509,RMVar_hsa_circ_176956,RMVar_hsa_circ_176957,RMVar_hsa_circ_176955,RMVar_hsa_circ_176952,RMVar_hsa_circ_176953,RMVar_hsa_circ_61486,RMVar_hsa_circ_296160,RMVar_hsa_circ_176960 11815 RMVar_ID_11815 Human_SNP_ID_596810497 A-to-I Human chr16 + 19648721 19648721 19648721 GAAATGCTGTCTCTACTAAAAATACCAAAGTTAGTCAGGCGGGGTGGCAGGCACCTGTTGTCCCA GAAATGCTGTCTCTACTAAAAATACCAAAGTTGGTCAGGCGGGGTGGCAGGCACCTGTTGTCCCA A G VPS35L Ensembl:ENSG00000103544 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1452215805 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_377326,RMVar_hsa_circ_104887,RMVar_hsa_circ_89821,RMVar_hsa_circ_284533,RMVar_hsa_circ_10393,RMVar_hsa_circ_176923,RMVar_hsa_circ_85709,RMVar_hsa_circ_369450,RMVar_hsa_circ_287757,RMVar_hsa_circ_176925,RMVar_hsa_circ_176926,RMVar_hsa_circ_287430,RMVar_hsa_circ_124672,RMVar_hsa_circ_273723,RMVar_hsa_circ_176932,RMVar_hsa_circ_176933,RMVar_hsa_circ_176928,RMVar_hsa_circ_176930,RMVar_hsa_circ_176931,RMVar_hsa_circ_176929,RMVar_hsa_circ_18908,RMVar_hsa_circ_30805,RMVar_hsa_circ_16385,RMVar_hsa_circ_321996,RMVar_hsa_circ_176946,RMVar_hsa_circ_344504,RMVar_hsa_circ_176950,RMVar_hsa_circ_176951,RMVar_hsa_circ_176954,RMVar_hsa_circ_25052,RMVar_hsa_circ_337162,RMVar_hsa_circ_300765,RMVar_hsa_circ_278485,RMVar_hsa_circ_176955,RMVar_hsa_circ_176952,RMVar_hsa_circ_176953,RMVar_hsa_circ_61486,RMVar_hsa_circ_86215,RMVar_hsa_circ_283684,RMVar_hsa_circ_176962,RMVar_hsa_circ_310172,RMVar_hsa_circ_330114,RMVar_hsa_circ_176963,RMVar_hsa_circ_297710,RMVar_hsa_circ_315233,RMVar_hsa_circ_283128,RMVar_hsa_circ_96039,RMVar_hsa_circ_176965,RMVar_hsa_circ_176967,RMVar_hsa_circ_176966,RMVar_hsa_circ_176971,RMVar_hsa_circ_176964,RMVar_hsa_circ_176972,RMVar_hsa_circ_366129,RMVar_hsa_circ_284755,RMVar_hsa_circ_314118,RMVar_hsa_circ_280174,RMVar_hsa_circ_42626,RMVar_hsa_circ_176974,RMVar_hsa_circ_176976,RMVar_hsa_circ_176975,RMVar_hsa_circ_176973,RMVar_hsa_circ_359633,RMVar_hsa_circ_289543,RMVar_hsa_circ_176979 11816 RMVar_ID_11816 Human_SNP_ID_596818373 A-to-I Human chr16 + 19680670 19680670 19680670 GCGGTGGCTCATGCCTTTAATCCCAGCAGTTCAGGAGGCCAAGGCAGGTGGATCGCTTGAGCCCA GCGGTGGCTCATGCCTTTAATCCCAGCAGTTCGGGAGGCCAAGGCAGGTGGATCGCTTGAGCCCA A G VPS35L Ensembl:ENSG00000103544 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1412037607 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_284533,RMVar_hsa_circ_10393,RMVar_hsa_circ_85709,RMVar_hsa_circ_287757,RMVar_hsa_circ_176926,RMVar_hsa_circ_124672,RMVar_hsa_circ_176928,RMVar_hsa_circ_176930,RMVar_hsa_circ_176929,RMVar_hsa_circ_18908,RMVar_hsa_circ_30805,RMVar_hsa_circ_176946,RMVar_hsa_circ_344504,RMVar_hsa_circ_300765,RMVar_hsa_circ_176952,RMVar_hsa_circ_176953,RMVar_hsa_circ_61486,RMVar_hsa_circ_86215,RMVar_hsa_circ_310172,RMVar_hsa_circ_176963,RMVar_hsa_circ_297710,RMVar_hsa_circ_315233,RMVar_hsa_circ_96039,RMVar_hsa_circ_176965,RMVar_hsa_circ_176964,RMVar_hsa_circ_284755,RMVar_hsa_circ_42626,RMVar_hsa_circ_176974,RMVar_hsa_circ_176973,RMVar_hsa_circ_176981,RMVar_hsa_circ_176980,RMVar_hsa_circ_277894,RMVar_hsa_circ_323129,RMVar_hsa_circ_376256,RMVar_hsa_circ_176982,RMVar_hsa_circ_176984,RMVar_hsa_circ_98481,RMVar_hsa_circ_311686,RMVar_hsa_circ_362997,RMVar_hsa_circ_176985,RMVar_hsa_circ_176983 11817 RMVar_ID_11817 Human_SNP_ID_596820636 A-to-I Human chr16 + 19689961 19689961 19689961 TTGAGACAGGATCTTGCTGTGTTGCTCATACTAGAGTGCAGTCATGTGATCATAGCTCATTGCAG TTGAGACAGGATCTTGCTGTGTTGCTCATACTTGAGTGCAGTCATGTGATCATAGCTCATTGCAG A T VPS35L Ensembl:ENSG00000103544 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1203502417 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_284533,RMVar_hsa_circ_85709,RMVar_hsa_circ_176926,RMVar_hsa_circ_124672,RMVar_hsa_circ_176928,RMVar_hsa_circ_176929,RMVar_hsa_circ_18908,RMVar_hsa_circ_176946,RMVar_hsa_circ_176952,RMVar_hsa_circ_27578,RMVar_hsa_circ_86215,RMVar_hsa_circ_297710,RMVar_hsa_circ_96039,RMVar_hsa_circ_176964,RMVar_hsa_circ_176973,RMVar_hsa_circ_376256,RMVar_hsa_circ_176982,RMVar_hsa_circ_176984,RMVar_hsa_circ_98481,RMVar_hsa_circ_362997,RMVar_hsa_circ_176985 11818 RMVar_ID_11818 Human_SNP_ID_596820642 A-to-I Human chr16 - 19689988 19689988 19689988 GGACTGCTTGAGCCCAGGAGTAGGTGGCTGCAATGAGCTATGATCACATGACTGCACTCTAGTAT GGACTGCTTGAGCCCAGGAGTAGGTGGCTGCATTGAGCTATGATCACATGACTGCACTCTAGTAT T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs911319011 Functional Loss SNV dbSNP153 33..33 33 - - - 11819 RMVar_ID_11819 Human_SNP_ID_596820643 A-to-I Human chr16 - 19689988 19689988 19689988 GGACTGCTTGAGCCCAGGAGTAGGTGGCTGCAATGAGCTATGATCACATGACTGCACTCTAGTAT GGACTGCTTGAGCCCAGGAGTAGGTGGCTGCAGTGAGCTATGATCACATGACTGCACTCTAGTAT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs911319011 Functional Loss SNV dbSNP153 33..33 33 - - - 11820 RMVar_ID_11820 Human_SNP_ID_596822017 A-to-I Human chr16 - 19694661 19694661 19694661 AACCCAGAGAGACCTCGGCTGTGTAAGAAATAAGAACTTAGCTGGGTGTGGTGGTACATGCCTGT AACCCAGAGAGACCTCGGCTGTGTAAGAAATAGGAACTTAGCTGGGTGTGGTGGTACATGCCTGT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs930182645 Functional Loss SNV dbSNP153 33..33 33 - - - 11821 RMVar_ID_11821 Human_SNP_ID_596822031 A-to-I Human chr16 - 19694708 19694708 19694708 AGCCAACCGTGCCCGGCCAAGCTCAGTATTTTAGGACTAGCCTGGGCAACCCAGAGAGACCTCGG AGCCAACCGTGCCCGGCCAAGCTCAGTATTTTCGGACTAGCCTGGGCAACCCAGAGAGACCTCGG T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1407833409 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12682488 11822 RMVar_ID_11822 Human_SNP_ID_596823302 A-to-I Human chr16 - 19699880 19699880 19699880 TTGCCCAGGCTGGTGTCAAACCCTTAGCCTCAAGCGATCCTCCTGTCTCAGCCTCCCAAAGTGCT TTGCCCAGGCTGGTGTCAAACCCTTAGCCTCAGGCGATCCTCCTGTCTCAGCCTCCCAAAGTGCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs989053548 Functional Loss SNV dbSNP153 33..33 33 - - - 11823 RMVar_ID_11823 Human_SNP_ID_596823763 A-to-I Human chr16 - 19701590 19701590 19701590 TGCCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAATCACCGTGCCCGGCCAATAAAT TGCCTGCCTCAGCCTCCCAAAGTGCTGGGATTGCAGGCGTGAATCACCGTGCCCGGCCAATAAAT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs529118881 Functional Loss SNV dbSNP153 33..33 33 - - - 11824 RMVar_ID_11824 Human_SNP_ID_596823884 A-to-I Human chr16 - 19702051 19702051 19702051 TAGACTCGGGAGGCGGAGGTTGGGGTGAGCCGAGATCACGCCATTGTACTCCAGCCTGGGCAACA TAGACTCGGGAGGCGGAGGTTGGGGTGAGCCGGGATCACGCCATTGTACTCCAGCCTGGGCAACA T C KNOP1 Ensembl:ENSG00000103550 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1310630387 Functional Loss SNV dbSNP153 33..33 33 - - - 11825 RMVar_ID_11825 Human_SNP_ID_596823903 A-to-I Human chr16 - 19702108 19702108 19702108 GTGGTGGCGCACTCCTGTTATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATTGCTTAGACTCG GTGGTGGCGCACTCCTGTTATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCTTAGACTCG T C KNOP1 Ensembl:ENSG00000103550 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1035494575 Functional Loss SNV dbSNP153 33..33 33 - - - 11826 RMVar_ID_11826 Human_SNP_ID_596823905 A-to-I Human chr16 - 19702112 19702112 19702112 GGGTGTGGTGGCGCACTCCTGTTATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATTGCTTAGA GGGTGTGGTGGCGCACTCCTGTTATCCCAGCTTCTCAGGAGGCTGAGGCAGGAGAATTGCTTAGA T A KNOP1 Ensembl:ENSG00000103550 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1381142130 Functional Loss SNV dbSNP153 33..33 33 - - - 11827 RMVar_ID_11827 Human_SNP_ID_596824042 A-to-I Human chr16 - 19702736 19702736 19702736 CACCTACCTCAGCCTCCCAAAGTGTTGGTATTACAGGCATGAGCCACCGCACCCAGGCCCCATCA CACCTACCTCAGCCTCCCAAAGTGTTGGTATTGCAGGCATGAGCCACCGCACCCAGGCCCCATCA T C KNOP1 Ensembl:ENSG00000103550 Protein coding 3'UTR GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1483118316 Functional Loss SNV dbSNP153 33..33 33 - - - 11828 RMVar_ID_11828 Human_SNP_ID_596824085 A-to-I Human chr16 - 19702943 19702943 19702943 ACGCCCAGGCTGGAGTGCAGAGGCGTGATCTCAGCTCACTGCAACCTCCACCTCCAGGGTTCAAG ACGCCCAGGCTGGAGTGCAGAGGCGTGATCTCGGCTCACTGCAACCTCCACCTCCAGGGTTCAAG T C KNOP1 Ensembl:ENSG00000103550 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1273729711 Functional Loss SNV dbSNP153 33..33 33 - - - 11829 RMVar_ID_11829 Human_SNP_ID_596824465 A-to-I Human chr16 - 19704190 19704190 19704190 TAATCCCGGCTACTCAGGAGGCTGACAGGAGAATCGCTTGAACCCGGGAGGTGGAGGTTGTAGTG TAATCCCGGCTACTCAGGAGGCTGACAGGAGAGTCGCTTGAACCCGGGAGGTGGAGGTTGTAGTG T C KNOP1 Ensembl:ENSG00000103550 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs138873958 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17564020,Human_RBP_ID_27439681 11830 RMVar_ID_11830 Human_SNP_ID_596824466 A-to-I Human chr16 - 19704190 19704190 19704190 TAATCCCGGCTACTCAGGAGGCTGACAGGAGAATCGCTTGAACCCGGGAGGTGGAGGTTGTAGTG TAATCCCGGCTACTCAGGAGGCTGACAGGAGACTCGCTTGAACCCGGGAGGTGGAGGTTGTAGTG T G KNOP1 Ensembl:ENSG00000103550 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs138873958 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17564020,Human_RBP_ID_27439681 11831 RMVar_ID_11831 Human_SNP_ID_596824469 A-to-I Human chr16 - 19704196 19704196 19704196 GGCTTGTAATCCCGGCTACTCAGGAGGCTGACAGGAGAATCGCTTGAACCCGGGAGGTGGAGGTT GGCTTGTAATCCCGGCTACTCAGGAGGCTGACGGGAGAATCGCTTGAACCCGGGAGGTGGAGGTT T C KNOP1 Ensembl:ENSG00000103550 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1166188382 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6497979,Human_RBP_ID_17564020,Human_RBP_ID_17872806 11832 RMVar_ID_11832 Human_SNP_ID_596824494 A-to-I Human chr16 - 19704265 19704265 19704265 CTGACCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCTGGGTGGGTGTGGTGT CTGACCAACATGGTGAAACCCCGTCTCTACTACAAATACAAAAATTAGCTGGGTGGGTGTGGTGT T G KNOP1 Ensembl:ENSG00000103550 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1416373769 Functional Loss SNV dbSNP153 33..33 33 - - - 11833 RMVar_ID_11833 Human_SNP_ID_596824891 A-to-I Human chr16 - 19705695 19705695 19705695 TAGAGATGGGGTCTCACTATATTGTCCAGGCTAGTCCCAAACTCCTGGACTCAACTCATGCTCCT TAGAGATGGGGTCTCACTATATTGTCCAGGCTGGTCCCAAACTCCTGGACTCAACTCATGCTCCT T C KNOP1 Ensembl:ENSG00000103550 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs548451872 Functional Loss SNV dbSNP153 33..33 33 - - - 11834 RMVar_ID_11834 Human_SNP_ID_596824940 A-to-I Human chr16 - 19705886 19705886 19705886 GATCCCAGGGACGTGTGTGTGTGTTTTGAGATAGGCTCTCACTCTGTCACCCAGGCTGGAGTGTA GATCCCAGGGACGTGTGTGTGTGTTTTGAGATGGGCTCTCACTCTGTCACCCAGGCTGGAGTGTA T C KNOP1 Ensembl:ENSG00000103550 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1405320803 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1513557,Human_RBP_ID_1839075,Human_RBP_ID_26445872,Human_RBP_ID_26939536,Human_RBP_ID_27439701 11835 RMVar_ID_11835 Human_SNP_ID_596829097 A-to-I Human chr16 + 19719736 19719736 19719736 TTGCTCTGTCGCCCAGGCTGGAATGCAGTGGCACTGGCTGGGCTCACTGCAACCTCCGCCTCCCG TTGCTCTGTCGCCCAGGCTGGAATGCAGTGGCTCTGGCTGGGCTCACTGCAACCTCCGCCTCCCG A T IQCK Ensembl:ENSG00000174628 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1244187577 Functional Loss SNV dbSNP153 33..33 33 - - - 11836 RMVar_ID_11836 Human_SNP_ID_596833617 A-to-I Human chr16 + 19736326 19736326 19736326 TGCTCTGTTTTCAGGCTGGGGTGCAGTGGCGTAATCATGGCACACTGCAGCCTCAACCTCCAGGG TGCTCTGTTTTCAGGCTGGGGTGCAGTGGCGTGATCATGGCACACTGCAGCCTCAACCTCCAGGG A G IQCK Ensembl:ENSG00000174628 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973841062 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_333901,RMVar_hsa_circ_23449,RMVar_hsa_circ_176997,RMVar_hsa_circ_280483,RMVar_hsa_circ_302670,RMVar_hsa_circ_301156,RMVar_hsa_circ_176998,RMVar_hsa_circ_176996 11837 RMVar_ID_11837 Human_SNP_ID_596848226 A-to-I Human chr16 + 19799787 19799787 19799787 GCTACTCAGGATGCTGAGTGGGAGGATCACTTAAGCCCTGGGAGGTCGAGACTGCAGTGAGCTCT GCTACTCAGGATGCTGAGTGGGAGGATCACTTGAGCCCTGGGAGGTCGAGACTGCAGTGAGCTCT A G IQCK Ensembl:ENSG00000174628 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1055719244 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42725,RMVar_hsa_circ_301156,RMVar_hsa_circ_176999,RMVar_hsa_circ_176996,RMVar_hsa_circ_306815,RMVar_hsa_circ_177002,RMVar_hsa_circ_177004,RMVar_hsa_circ_320158 11838 RMVar_ID_11838 Human_SNP_ID_596863151 A-to-I Human chr16 - 19863792 19863792 19863792 GAGGTCCTATAAGAATCGAATGCCAGCTGGGCACAGTGACTCATGCCTGTAATCCCAGCACTTTG GAGGTCCTATAAGAATCGAATGCCAGCTGGGCGCAGTGACTCATGCCTGTAATCCCAGCACTTTG T C GPRC5B Ensembl:ENSG00000167191 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1297102220 Functional Loss SNV dbSNP153 33..33 33 - - - 11839 RMVar_ID_11839 Human_SNP_ID_597078021 A-to-I Human chr16 - 20739304 20739304 20739304 GTGTGTAGTGGCATGCGCCTGTAATCACAGCTACTTGGGAGGCTGAGGCAGGAAAATTGGTTGAA GTGTGTAGTGGCATGCGCCTGTAATCACAGCTGCTTGGGAGGCTGAGGCAGGAAAATTGGTTGAA T C THUMPD1 Ensembl:ENSG00000066654 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs760411880 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95260,RMVar_hsa_circ_177009 11840 RMVar_ID_11840 Human_SNP_ID_597078060 A-to-I Human chr16 - 20739435 20739435 20739435 TGGGCATGGTAGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGAGTGGATCACCTGA TGGGCATGGTAGCTCACACCTGTAATCCCAGCGCTTTGGGAGGCTGAGGCGAGTGGATCACCTGA T C THUMPD1 Ensembl:ENSG00000066654 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1430805799 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95260,RMVar_hsa_circ_177009 11841 RMVar_ID_11841 Human_SNP_ID_597078124 A-to-I Human chr16 - 20739641 20739641 20739641 AATTTTTGTATTTTTAGTAGAGACAAGGTTTCACCATGTTGGCTAGGCTGGTCTCGAACTTCTGA AATTTTTGTATTTTTAGTAGAGACAAGGTTTCGCCATGTTGGCTAGGCTGGTCTCGAACTTCTGA T C THUMPD1 Ensembl:ENSG00000066654 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1177037584 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95260,RMVar_hsa_circ_177009 11842 RMVar_ID_11842 Human_SNP_ID_597078151 A-to-I Human chr16 - 20739764 20739764 20739764 CAGGCTGGAGTGCAGTGGTGCAATCTCAGCTCACTGCAATATCTGCCTTCTGGGTTCAAGCGATT CAGGCTGGAGTGCAGTGGTGCAATCTCAGCTCGCTGCAATATCTGCCTTCTGGGTTCAAGCGATT T C THUMPD1 Ensembl:ENSG00000066654 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900996084 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95260,RMVar_hsa_circ_177009 11843 RMVar_ID_11843 Human_SNP_ID_597092549 A-to-I Human chr16 - 20803945 20803945 20803945 AGGAGACTGTGGTGGGAGGATTGCTTGAGCCCAGGAGATTAAGGCTGTAGTGAGTGGTGATCATA AGGAGACTGTGGTGGGAGGATTGCTTGAGCCCGGGAGATTAAGGCTGTAGTGAGTGGTGATCATA T C ERI2 Ensembl:ENSG00000196678 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1359854778 Functional Loss SNV dbSNP153 33..33 33 - - - 11844 RMVar_ID_11844 Human_SNP_ID_597094252 A-to-I Human chr16 + 20810513 20810513 20810513 CATTGCAACCTCTCCCTCCCAGCGATTCTCCTACCTCAGCCTCCTGAGTAGCTGGGATTACAGGC CATTGCAACCTCTCCCTCCCAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGC A G REXO5 Ensembl:ENSG00000005189 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs549051457 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27649,RMVar_hsa_circ_118061,RMVar_hsa_circ_358886,RMVar_hsa_circ_177015,RMVar_hsa_circ_358544 11845 RMVar_ID_11845 Human_SNP_ID_597096350 A-to-I Human chr16 + 20819806 20819806 20819806 TAGAGTCAGGATCTCCCTCTGTTGCCCAGGCTAAAGTGCAGTGGTACAATCTAAGCTCACTGCAG TAGAGTCAGGATCTCCCTCTGTTGCCCAGGCTGAAGTGCAGTGGTACAATCTAAGCTCACTGCAG A G REXO5 Ensembl:ENSG00000005189 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1478425130 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_177017,RMVar_hsa_circ_118061,RMVar_hsa_circ_358886,RMVar_hsa_circ_177015,RMVar_hsa_circ_358544,RMVar_hsa_circ_62068,RMVar_hsa_circ_307215,RMVar_hsa_circ_362662,RMVar_hsa_circ_76616,RMVar_hsa_circ_9186,RMVar_hsa_circ_36000,RMVar_hsa_circ_177016,RMVar_hsa_circ_353593 11846 RMVar_ID_11846 Human_SNP_ID_597109872 A-to-I Human chr16 - 20881324 20881324 20881324 TCGGTCATTGTAACCTCAAATTCCTGGGCTCAAGCAGTTCTCTCCCCTCAGCCTCCTGAGTAGCT TCGGTCATTGTAACCTCAAATTCCTGGGCTCAGGCAGTTCTCTCCCCTCAGCCTCCTGAGTAGCT T C DCUN1D3,ERI2 Ensembl:ENSG00000188215,Ensembl:ENSG00000196678 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886268708 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118793,RMVar_hsa_circ_177027 11847 RMVar_ID_11847 Human_SNP_ID_597111189 A-to-I Human chr16 - 20887178 20887178 20887178 CCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCACCCGCCACCACGCCCTGCTAATTTTTGT CCTGCCTCAGCCTCCCGAGTAGCTGGGATTACGGGCACCCGCCACCACGCCCTGCTAATTTTTGT T C DCUN1D3,ERI2 Ensembl:ENSG00000188215,Ensembl:ENSG00000196678 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1219217795 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_127523 RMVar_hsa_circ_118793,RMVar_hsa_circ_177027 11848 RMVar_ID_11848 Human_SNP_ID_597170401 A-to-I Human chr16 - 21119799 21119799 21119799 GAGGTCAGGAGTTCAATACCAGCCTAGCCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAA GAGGTCAGGAGTTCAATACCAGCCTAGCCAACGTGGTGAAACCCCGTCTCTACTAAAAATACAAA T C DNAH3 Ensembl:ENSG00000158486 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1295941752 Functional Loss SNV dbSNP153 33..33 33 - - - 11849 RMVar_ID_11849 Human_SNP_ID_597244687 A-to-I Human chr16 - 21424655 21424655 21424655 GCTTGCCAAGTTTAGGCTGGGCATGGTGACTCATGCCTCTAATCCCAGCATTTTGGGAGGCTGAG GCTTGCCAAGTTTAGGCTGGGCATGGTGACTCTTGCCTCTAATCCCAGCATTTTGGGAGGCTGAG T A NPIPB3 Ensembl:ENSG00000169246 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs1387649961 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77764,RMVar_hsa_circ_177046 11850 RMVar_ID_11850 Human_SNP_ID_597253772 A-to-I Human chr16 - 21504211 21504211 21504211 CCTCAAGTGATCCACCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGAGTCAGCCATCCATGG CCTCAAGTGATCCACCCACCTCGGCCTCCCAACGTGCTGGGATTACAGGAGTCAGCCATCCATGG T G SMG1P3 Ensembl:ENSG00000180747 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs541854897 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2454372,Human_miRNA_ID_2454373 RMVar_hsa_circ_118546,RMVar_hsa_circ_177056,RMVar_hsa_circ_119988,RMVar_hsa_circ_177069,RMVar_hsa_circ_113808,RMVar_hsa_circ_177076 11851 RMVar_ID_11851 Human_SNP_ID_597253830 A-to-I Human chr16 - 21504369 21504369 21504369 CGGCTCACTACAACCTCTGGCTCCTGGGTTCAAGCAATCCTCATGCCTCAGCTTCCCCAAATAGC CGGCTCACTACAACCTCTGGCTCCTGGGTTCACGCAATCCTCATGCCTCAGCTTCCCCAAATAGC T G SMG1P3 Ensembl:ENSG00000180747 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1389169810 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12684836 RMVar_hsa_circ_118546,RMVar_hsa_circ_177056,RMVar_hsa_circ_119988,RMVar_hsa_circ_177069,RMVar_hsa_circ_113808,RMVar_hsa_circ_177076 11852 RMVar_ID_11852 Human_SNP_ID_597253903 A-to-I Human chr16 - 21504583 21504583 21504583 GTCTGAAAAAAAAAATTTAATATTTTTTTTGTAGAGATGGGGGTCTCACTATGTTGCTCAGGCTG GTCTGAAAAAAAAAATTTAATATTTTTTTTGTGGAGATGGGGGTCTCACTATGTTGCTCAGGCTG T C SMG1P3 Ensembl:ENSG00000180747 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1233969195 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118546,RMVar_hsa_circ_177056,RMVar_hsa_circ_119988,RMVar_hsa_circ_177069,RMVar_hsa_circ_113808,RMVar_hsa_circ_177076 11853 RMVar_ID_11853 Human_SNP_ID_597254092 A-to-I Human chr16 - 21505034 21505034 21505034 CGTCTCCACTAAAAATACAAAAAAACAAAATTAGCCGGGCTTGGTGGCGGGCGCCTGTAATCCCA CGTCTCCACTAAAAATACAAAAAAACAAAATTCGCCGGGCTTGGTGGCGGGCGCCTGTAATCCCA T G SMG1P3 Ensembl:ENSG00000180747 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1165730180 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17372190,Human_RBP_ID_18513367,Human_RBP_ID_18530245 RMVar_hsa_circ_118546,RMVar_hsa_circ_177056,RMVar_hsa_circ_119988,RMVar_hsa_circ_177069,RMVar_hsa_circ_113808,RMVar_hsa_circ_177076 11854 RMVar_ID_11854 Human_SNP_ID_597255347 A-to-I Human chr16 - 21508230 21508229 21508231 GATCGCACCATTGCACTCCAGCCTGGGCGACAAGAGGGAGACTTCGTCTCAAAAAAAAAAGGAAA GATCGCACCATTGCACTCCAGCCTGGGCGAC__GAGGGAGACTTCGTCTCAAAAAAAAAAGGAAA CTT C SMG1P3 Ensembl:ENSG00000180747 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1431378831 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_2470161,Human_RBP_ID_9841192,Human_RBP_ID_18513368 Human_miRNA_ID_2956226,Human_miRNA_ID_2956227 RMVar_hsa_circ_118546,RMVar_hsa_circ_177056,RMVar_hsa_circ_119988,RMVar_hsa_circ_177069,RMVar_hsa_circ_113808,RMVar_hsa_circ_177076 11855 RMVar_ID_11855 Human_SNP_ID_597255424 A-to-I Human chr16 - 21508430 21508430 21508430 GGTGAACCCTTGTCTCAACTAAAAATACAAAAATTAGGTGGGCGTGGTGGCAGGTGTCGGTAATC GGTGAACCCTTGTCTCAACTAAAAATACAAAATTTAGGTGGGCGTGGTGGCAGGTGTCGGTAATC T A SMG1P3 Ensembl:ENSG00000180747 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1211866593 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18437252 RMVar_hsa_circ_118546,RMVar_hsa_circ_177056,RMVar_hsa_circ_119988,RMVar_hsa_circ_177069,RMVar_hsa_circ_113808,RMVar_hsa_circ_177076 11856 RMVar_ID_11856 Human_SNP_ID_597258429 A-to-I Human chr16 - 21516473 21516448 21516473 ACCATGCCCAGCTAATTTTTTGTATTTTTAGCAGAGACAGGACTTCACCATGTTGGCCAGGCTTG ACCATGCCCAGCTAATTTTTTGTATTTTTAGC_________________________CAGGCTTG GGCCAACATGGTGAAGTCCTGTCTCT G SMG1P3 Ensembl:ENSG00000180747 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1480692115 Functional Loss DEL dbSNP153 33..57 33 - - - Human_RBP_ID_2470206,Human_RBP_ID_6498973,Human_RBP_ID_12685091 RMVar_hsa_circ_118546,RMVar_hsa_circ_177056,RMVar_hsa_circ_119988,RMVar_hsa_circ_177069,RMVar_hsa_circ_113808,RMVar_hsa_circ_177076 11857 RMVar_ID_11857 Human_SNP_ID_597258487 A-to-I Human chr16 - 21516601 21516601 21516601 AGATGGAGTTTTGCTCTTACCCAGGCTGGAGTACAATGGCGCGATCTCGGCTCACTACAACCTCC AGATGGAGTTTTGCTCTTACCCAGGCTGGAGTGCAATGGCGCGATCTCGGCTCACTACAACCTCC T C SMG1P3 Ensembl:ENSG00000180747 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1356867239 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8252490,Human_RBP_ID_17372214 RMVar_hsa_circ_118546,RMVar_hsa_circ_177056,RMVar_hsa_circ_119988,RMVar_hsa_circ_177069,RMVar_hsa_circ_113808,RMVar_hsa_circ_177076 11858 RMVar_ID_11858 Human_SNP_ID_597258577 A-to-I Human chr16 - 21516866 21516866 21516866 TCACTGCAACCTCTGCTTCCTGGTTTTAAGCAATTCTCCTGCCTCAACCTCCGGGAGCTTAGATT TCACTGCAACCTCTGCTTCCTGGTTTTAAGCAGTTCTCCTGCCTCAACCTCCGGGAGCTTAGATT T C SMG1P3 Ensembl:ENSG00000180747 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1336308300 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17564030 RMVar_hsa_circ_118546,RMVar_hsa_circ_177056,RMVar_hsa_circ_119988,RMVar_hsa_circ_177069,RMVar_hsa_circ_113808,RMVar_hsa_circ_177076 11859 RMVar_ID_11859 Human_SNP_ID_597259067 A-to-I Human chr16 - 21518086 21518086 21518086 TCTACCGAGGTCAGGAGTCCGAGACCAGCCTGACCAACATGGTGAAACCCCATCTCTACTAAAAA TCTACCGAGGTCAGGAGTCCGAGACCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAA T C SMG1P3 Ensembl:ENSG00000180747 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1227551505 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9841208 RMVar_hsa_circ_118546,RMVar_hsa_circ_177056,RMVar_hsa_circ_119988,RMVar_hsa_circ_177069,RMVar_hsa_circ_113808,RMVar_hsa_circ_177076 11860 RMVar_ID_11860 Human_SNP_ID_597349213 A-to-I Human chr16 - 21868415 21868415 21868415 CTACACCCAGCTAATTTTTTTGTATTATTTGTAGACATGGGGTTTCGCCACGTTGCCCAGGCTAG CTACACCCAGCTAATTTTTTTGTATTATTTGTGGACATGGGGTTTCGCCACGTTGCCCAGGCTAG T C NPIPB4 Ensembl:ENSG00000185864 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1377697413 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6499227,Human_RBP_ID_12685991,Human_RBP_ID_17564035 RMVar_hsa_circ_119988,RMVar_hsa_circ_177069,RMVar_hsa_circ_113808,RMVar_hsa_circ_177076,RMVar_hsa_circ_82127,RMVar_hsa_circ_114678,RMVar_hsa_circ_177098,RMVar_hsa_circ_177099 11861 RMVar_ID_11861 Human_SNP_ID_597349215 A-to-I Human chr16 - 21868424 21868424 21868424 CACACTCCACTACACCCAGCTAATTTTTTTGTATTATTTGTAGACATGGGGTTTCGCCACGTTGC CACACTCCACTACACCCAGCTAATTTTTTTGTGTTATTTGTAGACATGGGGTTTCGCCACGTTGC T C NPIPB4 Ensembl:ENSG00000185864 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1390158809 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6499229,Human_RBP_ID_12685991 RMVar_hsa_circ_119988,RMVar_hsa_circ_177069,RMVar_hsa_circ_113808,RMVar_hsa_circ_177076,RMVar_hsa_circ_82127,RMVar_hsa_circ_114678,RMVar_hsa_circ_177098,RMVar_hsa_circ_177099 11862 RMVar_ID_11862 Human_SNP_ID_597349222 A-to-I Human chr16 - 21868434 21868434 21868434 GGATTACAGGCACACTCCACTACACCCAGCTAATTTTTTTGTATTATTTGTAGACATGGGGTTTC GGATTACAGGCACACTCCACTACACCCAGCTATTTTTTTTGTATTATTTGTAGACATGGGGTTTC T A NPIPB4 Ensembl:ENSG00000185864 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1392903092 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119988,RMVar_hsa_circ_177069,RMVar_hsa_circ_113808,RMVar_hsa_circ_177076,RMVar_hsa_circ_82127,RMVar_hsa_circ_114678,RMVar_hsa_circ_177098,RMVar_hsa_circ_177099 11863 RMVar_ID_11863 Human_SNP_ID_597364625 A-to-I Human chr16 + 21956329 21956329 21956329 ACTTTGTGAGGCCGAGGCGGGTGGATTGCCTGAGCTCAGGAGTTTGAGACCAGCCTGAGCTATGG ACTTTGTGAGGCCGAGGCGGGTGGATTGCCTGCGCTCAGGAGTTTGAGACCAGCCTGAGCTATGG A C UQCRC2 Ensembl:ENSG00000140740 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs748520076 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111801,RMVar_hsa_circ_177106 11864 RMVar_ID_11864 Human_SNP_ID_597364653 A-to-I Human chr16 + 21956469 21956469 21956469 GGGAGGCTGAGACAGGAGAATCGCTTGAATCCAGGAGGCAGACATTGCAATGACCCGAGATCGCA GGGAGGCTGAGACAGGAGAATCGCTTGAATCCGGGAGGCAGACATTGCAATGACCCGAGATCGCA A G UQCRC2 Ensembl:ENSG00000140740 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs75868694 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111801,RMVar_hsa_circ_177106 11865 RMVar_ID_11865 Human_SNP_ID_597367019 A-to-I Human chr16 + 21965945 21965945 21965945 AGCTCAAGCAGTCCTTCTGCCTATGCCTCTCAAAGTGCTGGGATTACAGGCATGAGCCATTGCAC AGCTCAAGCAGTCCTTCTGCCTATGCCTCTCAGAGTGCTGGGATTACAGGCATGAGCCATTGCAC A G UQCRC2 Ensembl:ENSG00000140740 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1377454985 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7292,RMVar_hsa_circ_3962,RMVar_hsa_circ_111801,RMVar_hsa_circ_326545,RMVar_hsa_circ_177106,RMVar_hsa_circ_371720,RMVar_hsa_circ_123497,RMVar_hsa_circ_177113,RMVar_hsa_circ_177109,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_331455,RMVar_hsa_circ_177119,RMVar_hsa_circ_301338,RMVar_hsa_circ_270153,RMVar_hsa_circ_81776,RMVar_hsa_circ_177121,RMVar_hsa_circ_177123,RMVar_hsa_circ_177124,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_54235,RMVar_hsa_circ_177125,RMVar_hsa_circ_177127,RMVar_hsa_circ_177128,RMVar_hsa_circ_177126,RMVar_hsa_circ_121920,RMVar_hsa_circ_320162,RMVar_hsa_circ_177129,RMVar_hsa_circ_177130 11866 RMVar_ID_11866 Human_SNP_ID_597367046 A-to-I Human chr16 + 21966058 21966058 21966058 AATAGGGGCTGGGCCCAGTGGCTCATGCGTGTAATCTCAGCACTTTGGGAGGCCAAGACAGAGGG AATAGGGGCTGGGCCCAGTGGCTCATGCGTGTGATCTCAGCACTTTGGGAGGCCAAGACAGAGGG A G UQCRC2 Ensembl:ENSG00000140740 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1281489799 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17564038 RMVar_hsa_circ_7292,RMVar_hsa_circ_3962,RMVar_hsa_circ_111801,RMVar_hsa_circ_326545,RMVar_hsa_circ_177106,RMVar_hsa_circ_371720,RMVar_hsa_circ_123497,RMVar_hsa_circ_177113,RMVar_hsa_circ_177109,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_331455,RMVar_hsa_circ_177119,RMVar_hsa_circ_301338,RMVar_hsa_circ_270153,RMVar_hsa_circ_81776,RMVar_hsa_circ_177121,RMVar_hsa_circ_177123,RMVar_hsa_circ_177124,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_54235,RMVar_hsa_circ_177125,RMVar_hsa_circ_177127,RMVar_hsa_circ_177128,RMVar_hsa_circ_177126,RMVar_hsa_circ_121920,RMVar_hsa_circ_320162,RMVar_hsa_circ_177129,RMVar_hsa_circ_177130 11867 RMVar_ID_11867 Human_SNP_ID_597367839 A-to-I Human chr16 + 21969464 21969464 21969464 CTGAGGAGGAGAATCGCTTGAACCCAGGAGGCAGTGATTGCAGTGAGCTGAGATCGTGCCACTGC CTGAGGAGGAGAATCGCTTGAACCCAGGAGGCGGTGATTGCAGTGAGCTGAGATCGTGCCACTGC A G UQCRC2 Ensembl:ENSG00000140740 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs566548166 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7292,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_81776,RMVar_hsa_circ_177121,RMVar_hsa_circ_177123,RMVar_hsa_circ_177124,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_118341,RMVar_hsa_circ_177130,RMVar_hsa_circ_338247,RMVar_hsa_circ_375797,RMVar_hsa_circ_272380,RMVar_hsa_circ_177133,RMVar_hsa_circ_177134,RMVar_hsa_circ_177132 11868 RMVar_ID_11868 Human_SNP_ID_597370901 A-to-I Human chr16 + 21982844 21982844 21982844 AAAATTAGCTGGGCATAGTGATACATGCCTGTAATCCCAGCTCCTTGGGAGGGTGAGGCAGAGAA AAAATTAGCTGGGCATAGTGATACATGCCTGTGATCCCAGCTCCTTGGGAGGGTGAGGCAGAGAA A G UQCRC2 Ensembl:ENSG00000140740 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs547585129 Functional Loss SNV dbSNP153 33..33 33 - - - 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_96562,RMVar_hsa_circ_177120,RMVar_hsa_circ_177128,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 11869 RMVar_ID_11869 Human_SNP_ID_597380961 A-to-I Human chr16 + 22027065 22027065 22027065 ATTCTATGTAATATACTAGAGAAATTCTCAAGAAAATCTAGGACTAGGATTTCAATATAATTTTA ATTCTATGTAATATACTAGAGAAATTCTCAAGGAAATCTAGGACTAGGATTTCAATATAATTTTA A G MOSMO Ensembl:ENSG00000185716 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1443007811 Functional Loss SNV dbSNP153 33..33 33 - - - 11870 RMVar_ID_11870 Human_SNP_ID_597380988 A-to-I Human chr16 + 22027187 22027187 22027187 AGAATGCAAAACTGTGTTATAGTGCTTTCATTAGGTTAACTGCGTTTCTAAACACCTGGAGAAAA AGAATGCAAAACTGTGTTATAGTGCTTTCATTGGGTTAACTGCGTTTCTAAACACCTGGAGAAAA A G MOSMO Ensembl:ENSG00000185716 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474272003 Functional Loss SNV dbSNP153 33..33 33 - - - 11871 RMVar_ID_11871 Human_SNP_ID_597427794 A-to-I Human chr16 + 22230331 22230331 22230331 CACTTCCTAGGTTCAAGTGATTCTTGTGCCTCAGCCTCCCAAGTAGCTGGAACCACAGGTGCACG CACTTCCTAGGTTCAAGTGATTCTTGTGCCTCCGCCTCCCAAGTAGCTGGAACCACAGGTGCACG A C EEF2K Ensembl:ENSG00000103319 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs940774065 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42456,RMVar_hsa_circ_177156,RMVar_hsa_circ_81910,RMVar_hsa_circ_50495 11872 RMVar_ID_11872 Human_SNP_ID_597431974 A-to-I Human chr16 + 22246479 22246479 22246479 CAGAGGTTGCAGTGAGCTGAGATCGTGCCACTACACTCCAGCCTGGGTGACAGAGTGAGACTCAG CAGAGGTTGCAGTGAGCTGAGATCGTGCCACTGCACTCCAGCCTGGGTGACAGAGTGAGACTCAG A G EEF2K Ensembl:ENSG00000103319 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223933642 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119412,RMVar_hsa_circ_42456,RMVar_hsa_circ_177156,RMVar_hsa_circ_81910,RMVar_hsa_circ_50495,RMVar_hsa_circ_338616,RMVar_hsa_circ_359078,RMVar_hsa_circ_337954,RMVar_hsa_circ_177158,RMVar_hsa_circ_177159 11873 RMVar_ID_11873 Human_SNP_ID_597434205 A-to-I Human chr16 + 22254795 22254795 22254795 GTAGCTCCTGATAAAAATGAGTTGCCAGGCACAGTGGCTCATGCTTGTAATCTCAGCACTTTGGA GTAGCTCCTGATAAAAATGAGTTGCCAGGCACGGTGGCTCATGCTTGTAATCTCAGCACTTTGGA A G EEF2K Ensembl:ENSG00000103319 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs949855773 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22583924 RMVar_hsa_circ_119412,RMVar_hsa_circ_42456,RMVar_hsa_circ_177156,RMVar_hsa_circ_81910,RMVar_hsa_circ_359078,RMVar_hsa_circ_61980,RMVar_hsa_circ_177158,RMVar_hsa_circ_110408,RMVar_hsa_circ_177162,RMVar_hsa_circ_376165,RMVar_hsa_circ_177164 11874 RMVar_ID_11874 Human_SNP_ID_597434414 A-to-I Human chr16 + 22255727 22255727 22255727 TGAGGCCAGTTCAAGACCAGCCTAGGCAACATAGTGAGACCTCGTCTCTATAAAAAAATTTAGAT TGAGGCCAGTTCAAGACCAGCCTAGGCAACATGGTGAGACCTCGTCTCTATAAAAAAATTTAGAT A G EEF2K Ensembl:ENSG00000103319 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1213538405 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119412,RMVar_hsa_circ_42456,RMVar_hsa_circ_177156,RMVar_hsa_circ_81910,RMVar_hsa_circ_359078,RMVar_hsa_circ_61980,RMVar_hsa_circ_177158,RMVar_hsa_circ_110408,RMVar_hsa_circ_177162,RMVar_hsa_circ_376165,RMVar_hsa_circ_177164 11875 RMVar_ID_11875 Human_SNP_ID_597436116 A-to-I Human chr16 + 22261898 22261898 22261898 ATGGTGGCATGTGCCTGTAATTCCAGCTACTTAGGAGGCTGAGGCAAGAGAATTGCTTGAACCTG ATGGTGGCATGTGCCTGTAATTCCAGCTACTTTGGAGGCTGAGGCAAGAGAATTGCTTGAACCTG A T EEF2K Ensembl:ENSG00000103319 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1328314514 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_177156,RMVar_hsa_circ_81910,RMVar_hsa_circ_359078,RMVar_hsa_circ_110408,RMVar_hsa_circ_177162,RMVar_hsa_circ_376165,RMVar_hsa_circ_177164,RMVar_hsa_circ_60217,RMVar_hsa_circ_94459,RMVar_hsa_circ_369496,RMVar_hsa_circ_177167,RMVar_hsa_circ_371746,RMVar_hsa_circ_127331,RMVar_hsa_circ_322778,RMVar_hsa_circ_177168,RMVar_hsa_circ_177170,RMVar_hsa_circ_177171,RMVar_hsa_circ_177169 11876 RMVar_ID_11876 Human_SNP_ID_597438042 A-to-I Human chr16 + 22268774 22268774 22268774 GGTTAGGAGTTCACAACTAGCCTGCCCAACATAGCAAAACCCTATCTCTACCAAAAATATAACAA GGTTAGGAGTTCACAACTAGCCTGCCCAACATGGCAAAACCCTATCTCTACCAAAAATATAACAA A G EEF2K Ensembl:ENSG00000103319 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs374149182 Functional Loss SNV dbSNP153 33..33 33 - - - 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 11877 RMVar_ID_11877 Human_SNP_ID_597439332 A-to-I Human chr16 + 22274239 22274239 22274239 CCAAGGAGGGCAGATCATGAGGTCAGGAGTTCAAGACCAGCCTGACCAACATGGTGAAACCCCAT CCAAGGAGGGCAGATCATGAGGTCAGGAGTTCGAGACCAGCCTGACCAACATGGTGAAACCCCAT A G EEF2K Ensembl:ENSG00000103319 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1385197230 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_177156,RMVar_hsa_circ_81910,RMVar_hsa_circ_74348,RMVar_hsa_circ_376165,RMVar_hsa_circ_177164,RMVar_hsa_circ_127331,RMVar_hsa_circ_177168,RMVar_hsa_circ_177174,RMVar_hsa_circ_335951 11878 RMVar_ID_11878 Human_SNP_ID_597439475 A-to-I Human chr16 + 22274757 22274757 22274757 AGCCTCCTGAGTAGGTGGGACTACAGGCATGTACCACCACACCCAGCTAAATTTTTAAATTTGTT AGCCTCCTGAGTAGGTGGGACTACAGGCATGTGCCACCACACCCAGCTAAATTTTTAAATTTGTT A G EEF2K Ensembl:ENSG00000103319 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1305846613 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_177156,RMVar_hsa_circ_81910,RMVar_hsa_circ_74348,RMVar_hsa_circ_376165,RMVar_hsa_circ_177164,RMVar_hsa_circ_127331,RMVar_hsa_circ_177168,RMVar_hsa_circ_177174,RMVar_hsa_circ_335951 11879 RMVar_ID_11879 Human_SNP_ID_597439487 A-to-I Human chr16 + 22274809 22274809 22274809 TTTTAAATTTGTTGGAGAGATGGGGTCTCACTATGTTGTTCAGACTGGTCTCGAACTCCTGGGCT TTTTAAATTTGTTGGAGAGATGGGGTCTCACTGTGTTGTTCAGACTGGTCTCGAACTCCTGGGCT A G EEF2K Ensembl:ENSG00000103319 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1424057552 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_177156,RMVar_hsa_circ_81910,RMVar_hsa_circ_74348,RMVar_hsa_circ_376165,RMVar_hsa_circ_177164,RMVar_hsa_circ_127331,RMVar_hsa_circ_177168,RMVar_hsa_circ_177174,RMVar_hsa_circ_335951 11880 RMVar_ID_11880 Human_SNP_ID_597439488 A-to-I Human chr16 + 22274809 22274809 22274809 TTTTAAATTTGTTGGAGAGATGGGGTCTCACTATGTTGTTCAGACTGGTCTCGAACTCCTGGGCT TTTTAAATTTGTTGGAGAGATGGGGTCTCACTTTGTTGTTCAGACTGGTCTCGAACTCCTGGGCT A T EEF2K Ensembl:ENSG00000103319 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1424057552 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_177156,RMVar_hsa_circ_81910,RMVar_hsa_circ_74348,RMVar_hsa_circ_376165,RMVar_hsa_circ_177164,RMVar_hsa_circ_127331,RMVar_hsa_circ_177168,RMVar_hsa_circ_177174,RMVar_hsa_circ_335951 11881 RMVar_ID_11881 Human_SNP_ID_597439675 A-to-I Human chr16 + 22275571 22275571 22275571 CACCATGTTGGCCAGGCTTGTCTCGAACTCCTAACCTCAGGCAGTCTACCTGCCTCTGCCTCCCA CACCATGTTGGCCAGGCTTGTCTCGAACTCCTGACCTCAGGCAGTCTACCTGCCTCTGCCTCCCA A G EEF2K Ensembl:ENSG00000103319 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1410853245 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_177156,RMVar_hsa_circ_81910,RMVar_hsa_circ_74348,RMVar_hsa_circ_376165,RMVar_hsa_circ_177164,RMVar_hsa_circ_127331,RMVar_hsa_circ_177168,RMVar_hsa_circ_177174,RMVar_hsa_circ_335951 11882 RMVar_ID_11882 Human_SNP_ID_597440082 A-to-I Human chr16 + 22277298 22277298 22277298 AGCTGGGACCATAGCCATGCACCACCATACCCAACTAACTTGTATTTTTTGTAGAGCTGGGGTTT AGCTGGGACCATAGCCATGCACCACCATACCCGACTAACTTGTATTTTTTGTAGAGCTGGGGTTT A G EEF2K Ensembl:ENSG00000103319 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1178858836 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_177156,RMVar_hsa_circ_81910,RMVar_hsa_circ_74348,RMVar_hsa_circ_376165,RMVar_hsa_circ_177164,RMVar_hsa_circ_127331,RMVar_hsa_circ_177168,RMVar_hsa_circ_177174,RMVar_hsa_circ_335951 11883 RMVar_ID_11883 Human_SNP_ID_597440222 A-to-I Human chr16 + 22278003 22278003 22278003 GAGGCAGGAAAATCACTTGAGTCCAGGAGTTCAAGACCAGCTTGGGCAACCTGGTAAGAGTGTGT GAGGCAGGAAAATCACTTGAGTCCAGGAGTTCGAGACCAGCTTGGGCAACCTGGTAAGAGTGTGT A G EEF2K Ensembl:ENSG00000103319 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1273567644 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_177156,RMVar_hsa_circ_81910,RMVar_hsa_circ_74348,RMVar_hsa_circ_376165,RMVar_hsa_circ_177164,RMVar_hsa_circ_127331,RMVar_hsa_circ_177168,RMVar_hsa_circ_177174,RMVar_hsa_circ_335951 11884 RMVar_ID_11884 Human_SNP_ID_597440245 A-to-I Human chr16 + 22278060 22278060 22278060 GAGTGTGTCTCTATAAAAAAATTTTAAAAATTAGCCAGGCGTGGTGACATGCCCCTGTCATCCCA GAGTGTGTCTCTATAAAAAAATTTTAAAAATTCGCCAGGCGTGGTGACATGCCCCTGTCATCCCA A C EEF2K Ensembl:ENSG00000103319 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1362520820 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_177156,RMVar_hsa_circ_81910,RMVar_hsa_circ_74348,RMVar_hsa_circ_376165,RMVar_hsa_circ_177164,RMVar_hsa_circ_127331,RMVar_hsa_circ_177168,RMVar_hsa_circ_177174,RMVar_hsa_circ_335951 11885 RMVar_ID_11885 Human_SNP_ID_597442141 A-to-I Human chr16 + 22285539 22285539 22285539 TTTCATTTGATGTTTCAAATAGCAAAGATGCTAGGTGCGGTGGCTCCCGCCTGTAATCTCAGCAC TTTCATTTGATGTTTCAAATAGCAAAGATGCTGGGTGCGGTGGCTCCCGCCTGTAATCTCAGCAC A G EEF2K Ensembl:ENSG00000103319 Protein coding 3'UTR GSE38233;GSE100210;GSE99789;GSE107867;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;ASD brains,cerebellum;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,29796672,30559470,31158229,31158229,32596459,32596459 RNA-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 11886 RMVar_ID_11886 Human_SNP_ID_597442157 A-to-I Human chr16 + 22285617 22285617 22285617 AAGGTGGGAGGATTGCTTGAGCTCAGGACTTCAAGACCAGCCTGGGTAAACATGGCGAGACCCTG AAGGTGGGAGGATTGCTTGAGCTCAGGACTTCTAGACCAGCCTGGGTAAACATGGCGAGACCCTG A T EEF2K Ensembl:ENSG00000103319 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs936125996 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26445878 RMVar_hsa_circ_177156,RMVar_hsa_circ_81910,RMVar_hsa_circ_127331,RMVar_hsa_circ_177168 11887 RMVar_ID_11887 Human_SNP_ID_597442542 A-to-I Human chr16 + 22287155 22287155 22287155 GGCTGAGGTGGGCGGATCACCTGAAGTCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAA GGCTGAGGTGGGCGGATCACCTGAAGTCAGCTTCTCGGGAGGCTGAGGCAGGAGAATCGCTTGAA A T EEF2K Ensembl:ENSG00000103319 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1368286092 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_177156,RMVar_hsa_circ_81910,RMVar_hsa_circ_127331,RMVar_hsa_circ_177168 11888 RMVar_ID_11888 Human_SNP_ID_597442547 A-to-I Human chr16 + 22287177 22287177 22287177 GAAGTCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCAGGAGGCAGAGGTTGCAGT GAAGTCAGCTACTCGGGAGGCTGAGGCAGGAGGATCGCTTGAACCCAGGAGGCAGAGGTTGCAGT A G EEF2K Ensembl:ENSG00000103319 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1351732826 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_177156,RMVar_hsa_circ_81910,RMVar_hsa_circ_127331,RMVar_hsa_circ_177168 11889 RMVar_ID_11889 Human_SNP_ID_597442710 A-to-I Human chr16 + 22287907 22287907 22287907 GCAGTGGCATGATCATAACTCATTGTAGGCTCAACCTCCTGGGCCCCAGTGATCCTCCTGCCTCA GCAGTGGCATGATCATAACTCATTGTAGGCTCCACCTCCTGGGCCCCAGTGATCCTCCTGCCTCA A C EEF2K Ensembl:ENSG00000103319 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs948208004 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12688914 Human_miRNA_ID_2994472 RMVar_hsa_circ_177156,RMVar_hsa_circ_81910,RMVar_hsa_circ_127331,RMVar_hsa_circ_177168 11890 RMVar_ID_11890 Human_SNP_ID_597442757 A-to-I Human chr16 + 22288088 22288088 22288088 TTGGCTCACTGCAACCTCTGCCTCCCAGGTTCAAGCGATTCTCCCTGTCTCGGCCTCCCGAGTAG TTGGCTCACTGCAACCTCTGCCTCCCAGGTTCGAGCGATTCTCCCTGTCTCGGCCTCCCGAGTAG A G EEF2K Ensembl:ENSG00000103319 Protein coding 3'UTR GSE47997;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611827,GSM3611828,GSM3611829 K562 cells&HepG2 cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BEP2D cell line - 23474544,29129909,31158229,31158229 RNA-Seq:(High) rs1490662487 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_177156,RMVar_hsa_circ_81910,RMVar_hsa_circ_127331,RMVar_hsa_circ_177168 11891 RMVar_ID_11891 Human_SNP_ID_597442957 A-to-I Human chr16 + 22288958 22288958 22288958 ATGGTGGCGCACACCTGTAGTCCCATCTGCTCAGGAGGCTGAGACAGGAGAATTGCTTAAAGCCG ATGGTGGCGCACACCTGTAGTCCCATCTGCTCGGGAGGCTGAGACAGGAGAATTGCTTAAAGCCG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1026097891 Functional Loss SNV dbSNP153 33..33 33 - - - 11892 RMVar_ID_11892 Human_SNP_ID_597444706 A-to-I Human chr16 + 22295619 22295619 22295619 CTCGCTGCAACCTCCGCCTCCCGGGTTCAAGCAACTCTCCCGCCTCAGCCTCCCGAGTAGCTGGG CTCGCTGCAACCTCCGCCTCCCGGGTTCAAGCGACTCTCCCGCCTCAGCCTCCCGAGTAGCTGGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs942782719 Functional Loss SNV dbSNP153 33..33 33 - - - 11893 RMVar_ID_11893 Human_SNP_ID_597449082 A-to-I Human chr16 + 22311069 22311069 22311069 CTCACTGAAACCTCTGCCTTCCGGTTTCAAGCAGTTCTCCTGTCTCAGACTCCCGAGTAGCTGGG CTCACTGAAACCTCTGCCTTCCGGTTTCAAGCGGTTCTCCTGTCTCAGACTCCCGAGTAGCTGGG A G POLR3E Ensembl:ENSG00000058600 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs935763207 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82200,RMVar_hsa_circ_17319,RMVar_hsa_circ_112539,RMVar_hsa_circ_177177,RMVar_hsa_circ_349584,RMVar_hsa_circ_80178,RMVar_hsa_circ_127587,RMVar_hsa_circ_177179,RMVar_hsa_circ_177182,RMVar_hsa_circ_118488,RMVar_hsa_circ_177183,RMVar_hsa_circ_126181,RMVar_hsa_circ_177184,RMVar_hsa_circ_268690,RMVar_hsa_circ_109524,RMVar_hsa_circ_123938,RMVar_hsa_circ_177186,RMVar_hsa_circ_177187,RMVar_hsa_circ_36770,RMVar_hsa_circ_177188 11894 RMVar_ID_11894 Human_SNP_ID_597449083 A-to-I Human chr16 + 22311083 22311083 22311083 TGCCTTCCGGTTTCAAGCAGTTCTCCTGTCTCAGACTCCCGAGTAGCTGGGACTACAGGTGCACA TGCCTTCCGGTTTCAAGCAGTTCTCCTGTCTCGGACTCCCGAGTAGCTGGGACTACAGGTGCACA A G POLR3E Ensembl:ENSG00000058600 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1331546680 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82200,RMVar_hsa_circ_17319,RMVar_hsa_circ_112539,RMVar_hsa_circ_177177,RMVar_hsa_circ_349584,RMVar_hsa_circ_80178,RMVar_hsa_circ_127587,RMVar_hsa_circ_177179,RMVar_hsa_circ_177182,RMVar_hsa_circ_118488,RMVar_hsa_circ_177183,RMVar_hsa_circ_126181,RMVar_hsa_circ_177184,RMVar_hsa_circ_268690,RMVar_hsa_circ_109524,RMVar_hsa_circ_123938,RMVar_hsa_circ_177186,RMVar_hsa_circ_177187,RMVar_hsa_circ_36770,RMVar_hsa_circ_177188 11895 RMVar_ID_11895 Human_SNP_ID_597449507 A-to-I Human chr16 + 22312756 22312756 22312756 GGGCTTGGTGGCACACACCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGGGAATCACTTGAA GGGCTTGGTGGCACACACCTGTAGTCCCAGCTGCTTGGGAGGCTGAGGCAGGGGAATCACTTGAA A G POLR3E Ensembl:ENSG00000058600 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs903113200 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82200,RMVar_hsa_circ_17319,RMVar_hsa_circ_112539,RMVar_hsa_circ_177177,RMVar_hsa_circ_349584,RMVar_hsa_circ_80178,RMVar_hsa_circ_127587,RMVar_hsa_circ_177179,RMVar_hsa_circ_177182,RMVar_hsa_circ_118488,RMVar_hsa_circ_177183,RMVar_hsa_circ_126181,RMVar_hsa_circ_177184,RMVar_hsa_circ_268690,RMVar_hsa_circ_109524,RMVar_hsa_circ_123938,RMVar_hsa_circ_177186,RMVar_hsa_circ_177187,RMVar_hsa_circ_36770,RMVar_hsa_circ_177188 11896 RMVar_ID_11896 Human_SNP_ID_597449511 A-to-I Human chr16 + 22312782 22312782 22312782 CCAGCTACTTGGGAGGCTGAGGCAGGGGAATCACTTGAACCGGGGAGGTGGAGGTTGCACTGAGC CCAGCTACTTGGGAGGCTGAGGCAGGGGAATCGCTTGAACCGGGGAGGTGGAGGTTGCACTGAGC A G POLR3E Ensembl:ENSG00000058600 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs377407779 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82200,RMVar_hsa_circ_17319,RMVar_hsa_circ_112539,RMVar_hsa_circ_177177,RMVar_hsa_circ_349584,RMVar_hsa_circ_80178,RMVar_hsa_circ_127587,RMVar_hsa_circ_177179,RMVar_hsa_circ_177182,RMVar_hsa_circ_118488,RMVar_hsa_circ_177183,RMVar_hsa_circ_126181,RMVar_hsa_circ_177184,RMVar_hsa_circ_268690,RMVar_hsa_circ_109524,RMVar_hsa_circ_123938,RMVar_hsa_circ_177186,RMVar_hsa_circ_177187,RMVar_hsa_circ_36770,RMVar_hsa_circ_177188 11897 RMVar_ID_11897 Human_SNP_ID_597454580 A-to-I Human chr16 + 22330143 22330143 22330143 CATCTAGGCCTGGAGTGCAGTGGTGCCATCTCAGCTCACGCCTCTTGCGTTCAAGCGATTCTTGT CATCTAGGCCTGGAGTGCAGTGGTGCCATCTCGGCTCACGCCTCTTGCGTTCAAGCGATTCTTGT A G POLR3E Ensembl:ENSG00000058600 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs898370239 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12689598 RMVar_hsa_circ_127810,RMVar_hsa_circ_177192,RMVar_hsa_circ_93989,RMVar_hsa_circ_177193 11898 RMVar_ID_11898 Human_SNP_ID_597455529 A-to-I Human chr16 + 22333401 22333401 22333401 TTGAACCTGGGAGGCAGAGGCTGCAGTGAGCCAAGATCATGCCGTTGCACTCCAGCCTGGGTAAC TTGAACCTGGGAGGCAGAGGCTGCAGTGAGCCGAGATCATGCCGTTGCACTCCAGCCTGGGTAAC A G POLR3E Ensembl:ENSG00000058600 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1490255612 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25197332 RMVar_hsa_circ_127810,RMVar_hsa_circ_177192,RMVar_hsa_circ_93989,RMVar_hsa_circ_177193 11899 RMVar_ID_11899 Human_SNP_ID_597469969 A-to-I Human chr16 - 22390958 22390958 22390958 GTGGTGGCGCATGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGTGGGAGGATTGGTTCAGCTGA GTGGTGGCGCATGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGTGGGAGGATTGGTTCAGCTGA T C CDR2 Ensembl:ENSG00000140743 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1414138682 Functional Loss SNV dbSNP153 33..33 33 - - - 11900 RMVar_ID_11900 Human_SNP_ID_597472435 A-to-I Human chr16 - 22401502 22401502 22401502 GAGACTACAGGAGTGCACCACCACACCTGGCTAAATTTTTATTTTGTGTAGAGACAGGGTTTTGC GAGACTACAGGAGTGCACCACCACACCTGGCTCAATTTTTATTTTGTGTAGAGACAGGGTTTTGC T G CDR2 Ensembl:ENSG00000140743 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs959551705 Functional Loss SNV dbSNP153 33..33 33 - - - 11901 RMVar_ID_11901 Human_SNP_ID_597474724 A-to-I Human chr16 - 22411733 22411733 22411733 CTGTAATTCCAGCTATTTGGGAGGCTGAGGCAAGAGAATCTCTTGAACCCGGGAGGCAGAGGTTG CTGTAATTCCAGCTATTTGGGAGGCTGAGGCAGGAGAATCTCTTGAACCCGGGAGGCAGAGGTTG T C CDR2 Ensembl:ENSG00000140743 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1426010287 Functional Loss SNV dbSNP153 33..33 33 - - - 11902 RMVar_ID_11902 Human_SNP_ID_597474761 A-to-I Human chr16 - 22411900 22411900 22411900 AATCTGGCTTGGTGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGCAGA AATCTGGCTTGGTGCAGTGGCTCACACCTGTAGTCCCAGCACTTTGGGAGGCTGAGGTGGGCAGA T C CDR2 Ensembl:ENSG00000140743 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1268336866 Functional Loss SNV dbSNP153 33..33 33 - - - 11903 RMVar_ID_11903 Human_SNP_ID_597474959 A-to-I Human chr16 - 22412696 22412696 22412696 TAAAAAAGTAAATAAATAAGTTTGAGGCTGCAATGAGCTATGATTGTACCACTTCACTCTCAGCC TAAAAAAGTAAATAAATAAGTTTGAGGCTGCAGTGAGCTATGATTGTACCACTTCACTCTCAGCC T C CDR2 Ensembl:ENSG00000140743 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs980942584 Functional Loss SNV dbSNP153 33..33 33 - - - 11904 RMVar_ID_11904 Human_SNP_ID_597476379 A-to-I Human chr16 - 22418241 22418241 22418241 GGCTCACTGTGACTTCTGCCTCCCGGGTTCCAATGATTCTCTTGCCTCAGCCTGCTGAGTAGCTG GGCTCACTGTGACTTCTGCCTCCCGGGTTCCAGTGATTCTCTTGCCTCAGCCTGCTGAGTAGCTG T C CDR2 Ensembl:ENSG00000140743 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1442413435 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12690021 11905 RMVar_ID_11905 Human_SNP_ID_597477265 A-to-I Human chr16 - 22421857 22421857 22421857 TCGCCCAGGCTACAGTGCAGTGGTGCAATCACAGCCCACTGCAGCCTCGACCTCCGGAGCTCAAT TCGCCCAGGCTACAGTGCAGTGGTGCAATCACGGCCCACTGCAGCCTCGACCTCCGGAGCTCAAT T C CDR2,RRN3P3 Ensembl:ENSG00000140743,Ensembl:ENSG00000257122 Protein coding,Pseudogene intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1133587 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3510771,Human_RBP_ID_4356180,Human_RBP_ID_8429666 11906 RMVar_ID_11906 Human_SNP_ID_597481189 A-to-I Human chr16 + 22438567 22438567 22438567 ATTCCAGCAGTATTTGGAAATAATTTGCTAAGATGTTAGAATGTAACATTTGAAGACTTGTTAGA ATTCCAGCAGTATTTGGAAATAATTTGCTAAGCTGTTAGAATGTAACATTTGAAGACTTGTTAGA A C SMG1P1 Ensembl:ENSG00000237296 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1484042506 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1514204,Human_RBP_ID_1839532,Human_RBP_ID_3511453,Human_RBP_ID_9821826,Human_RBP_ID_17126143,Human_RBP_ID_17206588,Human_RBP_ID_17608284,Human_RBP_ID_18674994,Human_RBP_ID_25242729 11907 RMVar_ID_11907 Human_SNP_ID_597486557 A-to-I Human chr16 + 22477139 22477139 22477139 AGATCACACCACCGCACTCCAGCCTGGGCTACAGAGCCAGACTCTGTCTCAAAAGAAAAAAAAAA AGATCACACCACCGCACTCCAGCCTGGGCTACTGAGCCAGACTCTGTCTCAAAAGAAAAAAAAAA A T SMG1P1 Ensembl:ENSG00000237296 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1248875205 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25197471 RMVar_hsa_circ_98424,RMVar_hsa_circ_5257,RMVar_hsa_circ_87693,RMVar_hsa_circ_177199,RMVar_hsa_circ_112313,RMVar_hsa_circ_177200,RMVar_hsa_circ_117016,RMVar_hsa_circ_94646,RMVar_hsa_circ_177205,RMVar_hsa_circ_177207,RMVar_hsa_circ_177206,RMVar_hsa_circ_44,RMVar_hsa_circ_97826,RMVar_hsa_circ_120036,RMVar_hsa_circ_177209,RMVar_hsa_circ_100965,RMVar_hsa_circ_177213,RMVar_hsa_circ_87920,RMVar_hsa_circ_177214,RMVar_hsa_circ_119142,RMVar_hsa_circ_177215,RMVar_hsa_circ_177216,RMVar_hsa_circ_97952,RMVar_hsa_circ_86174,RMVar_hsa_circ_80359,RMVar_hsa_circ_177217,RMVar_hsa_circ_103940,RMVar_hsa_circ_177218,RMVar_hsa_circ_83425,RMVar_hsa_circ_84657,RMVar_hsa_circ_177219,RMVar_hsa_circ_177221,RMVar_hsa_circ_177222,RMVar_hsa_circ_177220 11908 RMVar_ID_11908 Human_SNP_ID_597486768 A-to-I Human chr16 + 22477968 22477968 22477968 AAAGTTAGCAGGGCATGGTGATGGGCACCTGTAATCTCAGCTACTTGGGAGACTGAGGCAGGGAG AAAGTTAGCAGGGCATGGTGATGGGCACCTGTGATCTCAGCTACTTGGGAGACTGAGGCAGGGAG A G SMG1P1 Ensembl:ENSG00000237296 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1406185855 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3510655,Human_RBP_ID_17565428 RMVar_hsa_circ_98424,RMVar_hsa_circ_5257,RMVar_hsa_circ_87693,RMVar_hsa_circ_177199,RMVar_hsa_circ_112313,RMVar_hsa_circ_177200,RMVar_hsa_circ_117016,RMVar_hsa_circ_94646,RMVar_hsa_circ_177205,RMVar_hsa_circ_177207,RMVar_hsa_circ_177206,RMVar_hsa_circ_44,RMVar_hsa_circ_97826,RMVar_hsa_circ_120036,RMVar_hsa_circ_177209,RMVar_hsa_circ_100965,RMVar_hsa_circ_177213,RMVar_hsa_circ_87920,RMVar_hsa_circ_177214,RMVar_hsa_circ_119142,RMVar_hsa_circ_177215,RMVar_hsa_circ_177216,RMVar_hsa_circ_97952,RMVar_hsa_circ_86174,RMVar_hsa_circ_80359,RMVar_hsa_circ_177217,RMVar_hsa_circ_103940,RMVar_hsa_circ_177218,RMVar_hsa_circ_83425,RMVar_hsa_circ_84657,RMVar_hsa_circ_177219,RMVar_hsa_circ_177221,RMVar_hsa_circ_177222,RMVar_hsa_circ_177220 11909 RMVar_ID_11909 Human_SNP_ID_597487435 A-to-I Human chr16 - 22481037 22481037 22481037 CCACGGTGCACTAGTTGGACACGGCAAACATCAACACATCTATGAAAGAACGAAATAGACAAAGC CCACGGTGCACTAGTTGGACACGGCAAACATCCACACATCTATGAAAGAACGAAATAGACAAAGC T G - - Other Unknown GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1383930799 Functional Loss SNV dbSNP153 33..33 33 - - - 11910 RMVar_ID_11910 Human_SNP_ID_597632905 A-to-I Human chr16 - 23063590 23063590 23063590 TCTGCTGTTTTTCTGATCATTGGCGAGATTGTAAAGTATTTTGCAAGCAGAAGTGGAATTGGATA TCTGCTGTTTTTCTGATCATTGGCGAGATTGTGAAGTATTTTGCAAGCAGAAGTGGAATTGGATA T C USP31,AC127459.1 Ensembl:ENSG00000103404,Ensembl:ENSG00000260566 Protein coding,lincRNA 3'UTR,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs557787665 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1839604,Human_RBP_ID_5097525,Human_RBP_ID_5574517,Human_RBP_ID_6500560,Human_RBP_ID_12690981,Human_RBP_ID_18284773 11911 RMVar_ID_11911 Human_SNP_ID_597637601 A-to-I Human chr16 - 23079993 23079993 23079993 GAGGGACCCTGAGGACTACATCTATGACCTGTATGCTGTGTGCAATCACCATGGCACCATGCAAG GAGGGACCCTGAGGACTACATCTATGACCTGTGTGCTGTGTGCAATCACCATGGCACCATGCAAG T C USP31 Ensembl:ENSG00000103404 Protein coding CDS GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs768194892 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9372448,Human_RBP_ID_18985711,Human_RBP_ID_26328096,Human_RBP_ID_27810976 Human_Splice_Rec_1691787 Human_miRNA_ID_887405,Human_miRNA_ID_2275556,Human_miRNA_ID_2401450,Human_miRNA_ID_2495376,Human_miRNA_ID_2501296,Human_miRNA_ID_3109330,Human_miRNA_ID_3110774 RMVar_hsa_circ_177231,RMVar_hsa_circ_118059,RMVar_hsa_circ_326718,RMVar_hsa_circ_90318,RMVar_hsa_circ_177228,RMVar_hsa_circ_177229,RMVar_hsa_circ_273013,RMVar_hsa_circ_366051,RMVar_hsa_circ_177230,RMVar_hsa_circ_306998,RMVar_hsa_circ_177232 11912 RMVar_ID_11912 Human_SNP_ID_597652050 A-to-I Human chr16 - 23137540 23137536 23137540 AAACGTCCAAAGGAAGAGGACAGAATAAGTAAATTATCACTTATCAATGTGATACCACCATATAA AAACGTCCAAAGGAAGAGGACAGAATAAGTAA____TCACTTATCAATGTGATACCACCATATAA ATAAT A USP31 Ensembl:ENSG00000103404 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1403746113 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_114228,RMVar_hsa_circ_177242 11913 RMVar_ID_11913 Human_SNP_ID_597652051 A-to-I Human chr16 - 23137546 23137546 23137546 GGAGGAAAACGTCCAAAGGAAGAGGACAGAATAAGTAAATTATCACTTATCAATGTGATACCACC GGAGGAAAACGTCCAAAGGAAGAGGACAGAATGAGTAAATTATCACTTATCAATGTGATACCACC T C USP31 Ensembl:ENSG00000103404 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1434850027 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_818201 RMVar_hsa_circ_114228,RMVar_hsa_circ_177242 11914 RMVar_ID_11914 Human_SNP_ID_597724397 A-to-I Human chr16 + 23414518 23414518 23414518 TGGCGTGGTGGCGCATGCCTGTAGTCCCAGCTACTCAGGAGGCTGGGGTGGAAAGATGGCTTGAG TGGCGTGGTGGCGCATGCCTGTAGTCCCAGCTGCTCAGGAGGCTGGGGTGGAAAGATGGCTTGAG A G RN7SKP23 Ensembl:ENSG00000280039 Other exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1339190704 Functional Loss SNV dbSNP153 33..33 33 - - - 11915 RMVar_ID_11915 Human_SNP_ID_597725073 A-to-I Human chr16 - 23417510 23417510 23417510 TGCCCACGTCTGCCATCCAAAGTACTGGGATTACAGGCTTGAGCCACTGCACCCAGCCCCCTTTT TGCCCACGTCTGCCATCCAAAGTACTGGGATTGCAGGCTTGAGCCACTGCACCCAGCCCCCTTTT T C COG7 Ensembl:ENSG00000168434 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs912322649 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121571,RMVar_hsa_circ_177247,RMVar_hsa_circ_123543,RMVar_hsa_circ_305135,RMVar_hsa_circ_109774,RMVar_hsa_circ_115354,RMVar_hsa_circ_106130,RMVar_hsa_circ_177251,RMVar_hsa_circ_177255,RMVar_hsa_circ_93484,RMVar_hsa_circ_177256,RMVar_hsa_circ_177253,RMVar_hsa_circ_177254,RMVar_hsa_circ_177252,RMVar_hsa_circ_43396,RMVar_hsa_circ_177263,RMVar_hsa_circ_115003,RMVar_hsa_circ_50644,RMVar_hsa_circ_30546,RMVar_hsa_circ_105085,RMVar_hsa_circ_46654,RMVar_hsa_circ_103679,RMVar_hsa_circ_332554,RMVar_hsa_circ_177269,RMVar_hsa_circ_23086,RMVar_hsa_circ_372586,RMVar_hsa_circ_293620,RMVar_hsa_circ_313727,RMVar_hsa_circ_177271,RMVar_hsa_circ_177272,RMVar_hsa_circ_121531,RMVar_hsa_circ_279163,RMVar_hsa_circ_177276,RMVar_hsa_circ_98987,RMVar_hsa_circ_79418,RMVar_hsa_circ_177277,RMVar_hsa_circ_177274,RMVar_hsa_circ_177275,RMVar_hsa_circ_177273 11916 RMVar_ID_11916 Human_SNP_ID_597725074 A-to-I Human chr16 - 23417510 23417510 23417510 TGCCCACGTCTGCCATCCAAAGTACTGGGATTACAGGCTTGAGCCACTGCACCCAGCCCCCTTTT TGCCCACGTCTGCCATCCAAAGTACTGGGATTCCAGGCTTGAGCCACTGCACCCAGCCCCCTTTT T G COG7 Ensembl:ENSG00000168434 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs912322649 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121571,RMVar_hsa_circ_177247,RMVar_hsa_circ_123543,RMVar_hsa_circ_305135,RMVar_hsa_circ_109774,RMVar_hsa_circ_115354,RMVar_hsa_circ_106130,RMVar_hsa_circ_177251,RMVar_hsa_circ_177255,RMVar_hsa_circ_93484,RMVar_hsa_circ_177256,RMVar_hsa_circ_177253,RMVar_hsa_circ_177254,RMVar_hsa_circ_177252,RMVar_hsa_circ_43396,RMVar_hsa_circ_177263,RMVar_hsa_circ_115003,RMVar_hsa_circ_50644,RMVar_hsa_circ_30546,RMVar_hsa_circ_105085,RMVar_hsa_circ_46654,RMVar_hsa_circ_103679,RMVar_hsa_circ_332554,RMVar_hsa_circ_177269,RMVar_hsa_circ_23086,RMVar_hsa_circ_372586,RMVar_hsa_circ_293620,RMVar_hsa_circ_313727,RMVar_hsa_circ_177271,RMVar_hsa_circ_177272,RMVar_hsa_circ_121531,RMVar_hsa_circ_279163,RMVar_hsa_circ_177276,RMVar_hsa_circ_98987,RMVar_hsa_circ_79418,RMVar_hsa_circ_177277,RMVar_hsa_circ_177274,RMVar_hsa_circ_177275,RMVar_hsa_circ_177273 11917 RMVar_ID_11917 Human_SNP_ID_597725949 A-to-I Human chr16 - 23420882 23420882 23420882 AAAATTAGCCAGGTATAGTAGCATACACCTGTAGTACTAGCTACTCAGGAGGCTGGGGTGGGGAG AAAATTAGCCAGGTATAGTAGCATACACCTGTGGTACTAGCTACTCAGGAGGCTGGGGTGGGGAG T C COG7 Ensembl:ENSG00000168434 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1247326124 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17564059 RMVar_hsa_circ_121571,RMVar_hsa_circ_177247,RMVar_hsa_circ_123543,RMVar_hsa_circ_109774,RMVar_hsa_circ_115354,RMVar_hsa_circ_106130,RMVar_hsa_circ_177251,RMVar_hsa_circ_177255,RMVar_hsa_circ_93484,RMVar_hsa_circ_177253,RMVar_hsa_circ_177254,RMVar_hsa_circ_177252,RMVar_hsa_circ_50644,RMVar_hsa_circ_30546,RMVar_hsa_circ_105085,RMVar_hsa_circ_46654,RMVar_hsa_circ_332554,RMVar_hsa_circ_23086,RMVar_hsa_circ_372586,RMVar_hsa_circ_313727,RMVar_hsa_circ_177272,RMVar_hsa_circ_121531,RMVar_hsa_circ_37637,RMVar_hsa_circ_177276,RMVar_hsa_circ_98987,RMVar_hsa_circ_79418,RMVar_hsa_circ_177274,RMVar_hsa_circ_177275,RMVar_hsa_circ_177273 11918 RMVar_ID_11918 Human_SNP_ID_597725990 A-to-I Human chr16 - 23420968 23420968 23420968 AGGTGAGGGAGTCATTTGATTCTAGGAGTTCAAGATCAGCTCTGGAAACATATACCCCATCTCTA AGGTGAGGGAGTCATTTGATTCTAGGAGTTCAGGATCAGCTCTGGAAACATATACCCCATCTCTA T C COG7 Ensembl:ENSG00000168434 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1400090188 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17564060 RMVar_hsa_circ_121571,RMVar_hsa_circ_177247,RMVar_hsa_circ_123543,RMVar_hsa_circ_109774,RMVar_hsa_circ_115354,RMVar_hsa_circ_106130,RMVar_hsa_circ_177251,RMVar_hsa_circ_177255,RMVar_hsa_circ_93484,RMVar_hsa_circ_177253,RMVar_hsa_circ_177254,RMVar_hsa_circ_177252,RMVar_hsa_circ_50644,RMVar_hsa_circ_30546,RMVar_hsa_circ_105085,RMVar_hsa_circ_46654,RMVar_hsa_circ_332554,RMVar_hsa_circ_23086,RMVar_hsa_circ_372586,RMVar_hsa_circ_313727,RMVar_hsa_circ_177272,RMVar_hsa_circ_121531,RMVar_hsa_circ_37637,RMVar_hsa_circ_177276,RMVar_hsa_circ_98987,RMVar_hsa_circ_79418,RMVar_hsa_circ_177274,RMVar_hsa_circ_177275,RMVar_hsa_circ_177273 11919 RMVar_ID_11919 Human_SNP_ID_597726955 A-to-I Human chr16 - 23424904 23424904 23424904 GCCCCACGAGGTGGTAATGGTGCTGCTGATTCAGACCCTGGGGGCCCTCATGCCCTCGCTGCCCT GCCCCACGAGGTGGTAATGGTGCTGCTGATTCCGACCCTGGGGGCCCTCATGCCCTCGCTGCCCT T G COG7 Ensembl:ENSG00000168434 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1447896890 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9374018,Human_RBP_ID_12692635,Human_RBP_ID_22053049 Human_Splice_Rec_1691978 Human_miRNA_ID_2295926,Human_miRNA_ID_2469519 RMVar_hsa_circ_121571,RMVar_hsa_circ_177247,RMVar_hsa_circ_123543,RMVar_hsa_circ_109774,RMVar_hsa_circ_115354,RMVar_hsa_circ_106130,RMVar_hsa_circ_177251,RMVar_hsa_circ_177255,RMVar_hsa_circ_93484,RMVar_hsa_circ_177253,RMVar_hsa_circ_177254,RMVar_hsa_circ_177252,RMVar_hsa_circ_50644,RMVar_hsa_circ_30546,RMVar_hsa_circ_105085,RMVar_hsa_circ_46654,RMVar_hsa_circ_332554,RMVar_hsa_circ_23086,RMVar_hsa_circ_372586,RMVar_hsa_circ_313727,RMVar_hsa_circ_177272,RMVar_hsa_circ_121531,RMVar_hsa_circ_37637,RMVar_hsa_circ_177276,RMVar_hsa_circ_98987,RMVar_hsa_circ_79418,RMVar_hsa_circ_177274,RMVar_hsa_circ_177275,RMVar_hsa_circ_177273,RMVar_hsa_circ_333274 11920 RMVar_ID_11920 Human_SNP_ID_597728873 A-to-I Human chr16 - 23433160 23433160 23433160 GTTGAGGCCACAGTGACTATGGTCGCACCACTACACTTCAGCTTGGACAACAGAGCAAGCAAGAC GTTGAGGCCACAGTGACTATGGTCGCACCACTGCACTTCAGCTTGGACAACAGAGCAAGCAAGAC T C COG7 Ensembl:ENSG00000168434 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1345663262 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_177247,RMVar_hsa_circ_123543,RMVar_hsa_circ_109774,RMVar_hsa_circ_115354,RMVar_hsa_circ_106130,RMVar_hsa_circ_177251,RMVar_hsa_circ_93484,RMVar_hsa_circ_177253,RMVar_hsa_circ_177254,RMVar_hsa_circ_177252,RMVar_hsa_circ_50644,RMVar_hsa_circ_30546,RMVar_hsa_circ_105085,RMVar_hsa_circ_46654,RMVar_hsa_circ_23086,RMVar_hsa_circ_372586,RMVar_hsa_circ_313727,RMVar_hsa_circ_177272,RMVar_hsa_circ_121531,RMVar_hsa_circ_37637,RMVar_hsa_circ_98987,RMVar_hsa_circ_177274,RMVar_hsa_circ_177275,RMVar_hsa_circ_177273,RMVar_hsa_circ_333274 11921 RMVar_ID_11921 Human_SNP_ID_597732494 A-to-I Human chr16 - 23447483 23447483 23447483 TTTAAGGCCAGGTGCGGTGGCTTATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGTGGA TTTAAGGCCAGGTGCGGTGGCTTATGCCTGTAGTCCCAGCACTTTGGGAGGCTGAGGTGGGTGGA T C COG7 Ensembl:ENSG00000168434 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1446811203 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115354,RMVar_hsa_circ_177251,RMVar_hsa_circ_100179,RMVar_hsa_circ_177283 11922 RMVar_ID_11922 Human_SNP_ID_597732742 A-to-I Human chr16 - 23448506 23448506 23448506 GGAGTTCCAGACCAGCAGTTCCAGACCAGCCTAGACAACATAGCAAGACCCTATCTCTACAAAAA GGAGTTCCAGACCAGCAGTTCCAGACCAGCCTGGACAACATAGCAAGACCCTATCTCTACAAAAA T C COG7 Ensembl:ENSG00000168434 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs759760561 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115354,RMVar_hsa_circ_177251,RMVar_hsa_circ_100179,RMVar_hsa_circ_177283 11923 RMVar_ID_11923 Human_SNP_ID_597736460 A-to-I Human chr16 - 23462484 23462484 23462484 TCTGACCATACCAGCTGGGCGTGGTGGCTCACACCTGTAATCCTAGCAGTTTGGGAGGCCAGGGC TCTGACCATACCAGCTGGGCGTGGTGGCTCACGCCTGTAATCCTAGCAGTTTGGGAGGCCAGGGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1138342 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25198245 11924 RMVar_ID_11924 Human_SNP_ID_597736461 A-to-I Human chr16 - 23462486 23462486 23462486 AATCTGACCATACCAGCTGGGCGTGGTGGCTCACACCTGTAATCCTAGCAGTTTGGGAGGCCAGG AATCTGACCATACCAGCTGGGCGTGGTGGCTCGCACCTGTAATCCTAGCAGTTTGGGAGGCCAGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1061119 Functional Loss SNV dbSNP153 33..33 33 - - - 11925 RMVar_ID_11925 Human_SNP_ID_597736820 A-to-I Human chr16 - 23463845 23463845 23463845 CTCCGGCTTCAGCCTCTGGAGTAGCTGGGACTACAGGTGCATGCTGCCACGCCCAGCTAATGTTG CTCCGGCTTCAGCCTCTGGAGTAGCTGGGACTGCAGGTGCATGCTGCCACGCCCAGCTAATGTTG T C GGA2 Ensembl:ENSG00000103365 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs901265088 Functional Loss SNV dbSNP153 33..33 33 - - - 11926 RMVar_ID_11926 Human_SNP_ID_597737134 A-to-I Human chr16 - 23465153 23465153 23465153 AGTGAGACCGTGTCTCTGTTTTTTTAAAAGCTAGTTGTTGACCAGCTACCCTGAGCCAGGCACCA AGTGAGACCGTGTCTCTGTTTTTTTAAAAGCTGGTTGTTGACCAGCTACCCTGAGCCAGGCACCA T C GGA2 Ensembl:ENSG00000103365 Protein coding 3'UTR GSE38233;GSE100210;GSE107867;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,cerebellum;ASD brains,frontal_cortex - 24183664,29129909,30559470,30559470 RNA-Seq:(High) rs1305719470 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2470991,Human_RBP_ID_3492832,Human_RBP_ID_12693005,Human_RBP_ID_26444919 11927 RMVar_ID_11927 Human_SNP_ID_597737161 A-to-I Human chr16 - 23465260 23465260 23465260 TAGTTATTGGCTGTGCACAGTGGCTCACGCCTATAATCCCAGCATTTTGGGAGGCTGAGTGGGAT TAGTTATTGGCTGTGCACAGTGGCTCACGCCTGTAATCCCAGCATTTTGGGAGGCTGAGTGGGAT T C GGA2 Ensembl:ENSG00000103365 Protein coding 3'UTR GSE38233;GSE100210;GSE112787 cultured B-cells;HepG2 cell line;293 Flip-In T-REx cells,empty vector - 24183664,29129909,29967493 RNA-Seq:(High) rs1141325 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12693015,Human_RBP_ID_26444920 11928 RMVar_ID_11928 Human_SNP_ID_597738682 A-to-I Human chr16 - 23470743 23470743 23470743 TTTTGTTTTTTGTTTGTTTGTTTGTTTGAGACAGAGTCTCGCTCTGTCACTTAGGCTGGAGTGCA TTTTGTTTTTTGTTTGTTTGTTTGTTTGAGACGGAGTCTCGCTCTGTCACTTAGGCTGGAGTGCA T C GGA2 Ensembl:ENSG00000103365 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1410490159 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4063,RMVar_hsa_circ_97737,RMVar_hsa_circ_360615,RMVar_hsa_circ_38165,RMVar_hsa_circ_64631,RMVar_hsa_circ_6621,RMVar_hsa_circ_177289,RMVar_hsa_circ_177286 11929 RMVar_ID_11929 Human_SNP_ID_597740056 A-to-I Human chr16 - 23475457 23475457 23475457 CATCTGGCGCATTAGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGACGGATCACC CATCTGGCGCATTAGCTCACGCCTGTAATCCCGGCACTTTGGGAGGCCGAGGCGGACGGATCACC T C GGA2 Ensembl:ENSG00000103365 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs907896620 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4063,RMVar_hsa_circ_97737,RMVar_hsa_circ_360615,RMVar_hsa_circ_38165,RMVar_hsa_circ_64631,RMVar_hsa_circ_6621,RMVar_hsa_circ_76697,RMVar_hsa_circ_177286,RMVar_hsa_circ_287907,RMVar_hsa_circ_372268,RMVar_hsa_circ_378253,RMVar_hsa_circ_339275,RMVar_hsa_circ_177292,RMVar_hsa_circ_177293,RMVar_hsa_circ_177294,RMVar_hsa_circ_177291 11930 RMVar_ID_11930 Human_SNP_ID_597740103 A-to-I Human chr16 - 23475658 23475658 23475658 CTCAAATGATCCACCTGCCTCGGCCTCCCAAAATGCTGGGATTACAGGCGTGAGCCACCGTGCCC CTCAAATGATCCACCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGTGCCC T C GGA2 Ensembl:ENSG00000103365 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1253675131 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4063,RMVar_hsa_circ_97737,RMVar_hsa_circ_360615,RMVar_hsa_circ_38165,RMVar_hsa_circ_64631,RMVar_hsa_circ_6621,RMVar_hsa_circ_76697,RMVar_hsa_circ_177286,RMVar_hsa_circ_287907,RMVar_hsa_circ_372268,RMVar_hsa_circ_378253,RMVar_hsa_circ_339275,RMVar_hsa_circ_177292,RMVar_hsa_circ_177293,RMVar_hsa_circ_177294,RMVar_hsa_circ_177291 11931 RMVar_ID_11931 Human_SNP_ID_597740123 A-to-I Human chr16 - 23475721 23475721 23475721 TTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTCGGCCGGGCTGGTCTTGAACTCCTGACCT TTTTGTATTTTTAGTAGAGATGGGGTTTCACCGTGTCGGCCGGGCTGGTCTTGAACTCCTGACCT T C GGA2 Ensembl:ENSG00000103365 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904477937 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4063,RMVar_hsa_circ_97737,RMVar_hsa_circ_360615,RMVar_hsa_circ_38165,RMVar_hsa_circ_64631,RMVar_hsa_circ_6621,RMVar_hsa_circ_76697,RMVar_hsa_circ_177286,RMVar_hsa_circ_287907,RMVar_hsa_circ_372268,RMVar_hsa_circ_378253,RMVar_hsa_circ_339275,RMVar_hsa_circ_177292,RMVar_hsa_circ_177293,RMVar_hsa_circ_177294,RMVar_hsa_circ_177291 11932 RMVar_ID_11932 Human_SNP_ID_597740430 A-to-I Human chr16 - 23477014 23477014 23477014 CCGGAAAGTCGAGGCTGCAGTGAGCCATTACTATGCCACTGCATTCCAGCCTGGGCAGCAGAGTG CCGGAAAGTCGAGGCTGCAGTGAGCCATTACTTTGCCACTGCATTCCAGCCTGGGCAGCAGAGTG T A GGA2 Ensembl:ENSG00000103365 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs941133150 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25198326 RMVar_hsa_circ_4063,RMVar_hsa_circ_97737,RMVar_hsa_circ_360615,RMVar_hsa_circ_38165,RMVar_hsa_circ_64631,RMVar_hsa_circ_6621,RMVar_hsa_circ_76697,RMVar_hsa_circ_177286,RMVar_hsa_circ_287907,RMVar_hsa_circ_372268,RMVar_hsa_circ_378253,RMVar_hsa_circ_339275,RMVar_hsa_circ_177292,RMVar_hsa_circ_177293,RMVar_hsa_circ_177294,RMVar_hsa_circ_177291 11933 RMVar_ID_11933 Human_SNP_ID_597740431 A-to-I Human chr16 - 23477014 23477014 23477014 CCGGAAAGTCGAGGCTGCAGTGAGCCATTACTATGCCACTGCATTCCAGCCTGGGCAGCAGAGTG CCGGAAAGTCGAGGCTGCAGTGAGCCATTACTGTGCCACTGCATTCCAGCCTGGGCAGCAGAGTG T C GGA2 Ensembl:ENSG00000103365 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs941133150 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25198326 RMVar_hsa_circ_4063,RMVar_hsa_circ_97737,RMVar_hsa_circ_360615,RMVar_hsa_circ_38165,RMVar_hsa_circ_64631,RMVar_hsa_circ_6621,RMVar_hsa_circ_76697,RMVar_hsa_circ_177286,RMVar_hsa_circ_287907,RMVar_hsa_circ_372268,RMVar_hsa_circ_378253,RMVar_hsa_circ_339275,RMVar_hsa_circ_177292,RMVar_hsa_circ_177293,RMVar_hsa_circ_177294,RMVar_hsa_circ_177291 11934 RMVar_ID_11934 Human_SNP_ID_597740456 A-to-I Human chr16 - 23477090 23477090 23477090 AAAATTAGCCAGGCGTGGTAGGTCATGACTGTAGTCCCAGCTGCTCAGGAGGCTGAGGTAGAAGG AAAATTAGCCAGGCGTGGTAGGTCATGACTGTCGTCCCAGCTGCTCAGGAGGCTGAGGTAGAAGG T G GGA2 Ensembl:ENSG00000103365 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1227336855 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12693225 RMVar_hsa_circ_4063,RMVar_hsa_circ_97737,RMVar_hsa_circ_360615,RMVar_hsa_circ_38165,RMVar_hsa_circ_64631,RMVar_hsa_circ_6621,RMVar_hsa_circ_76697,RMVar_hsa_circ_177286,RMVar_hsa_circ_287907,RMVar_hsa_circ_372268,RMVar_hsa_circ_378253,RMVar_hsa_circ_339275,RMVar_hsa_circ_177292,RMVar_hsa_circ_177293,RMVar_hsa_circ_177294,RMVar_hsa_circ_177291 11935 RMVar_ID_11935 Human_SNP_ID_597740487 A-to-I Human chr16 - 23477202 23477202 23477202 CATACCTGTAATCCCAGAACTTTGGGAGGCCAAGGCAGGTGGATCGCTTGAGCCCTGGAGTTCAA CATACCTGTAATCCCAGAACTTTGGGAGGCCAGGGCAGGTGGATCGCTTGAGCCCTGGAGTTCAA T C GGA2 Ensembl:ENSG00000103365 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1015494884 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17564061 RMVar_hsa_circ_4063,RMVar_hsa_circ_97737,RMVar_hsa_circ_360615,RMVar_hsa_circ_38165,RMVar_hsa_circ_64631,RMVar_hsa_circ_6621,RMVar_hsa_circ_76697,RMVar_hsa_circ_177286,RMVar_hsa_circ_287907,RMVar_hsa_circ_372268,RMVar_hsa_circ_378253,RMVar_hsa_circ_339275,RMVar_hsa_circ_177292,RMVar_hsa_circ_177293,RMVar_hsa_circ_177294,RMVar_hsa_circ_177291 11936 RMVar_ID_11936 Human_SNP_ID_597740730 A-to-I Human chr16 - 23478152 23478152 23478152 CTCTGTTGCCCAGGCTAGAGTGCAGTGGCACAATCTCGGCTCACTACAGCCTTTACCTCCTGAGT CTCTGTTGCCCAGGCTAGAGTGCAGTGGCACAGTCTCGGCTCACTACAGCCTTTACCTCCTGAGT T C GGA2 Ensembl:ENSG00000103365 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1350112304 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4063,RMVar_hsa_circ_97737,RMVar_hsa_circ_360615,RMVar_hsa_circ_38165,RMVar_hsa_circ_64631,RMVar_hsa_circ_6621,RMVar_hsa_circ_76697,RMVar_hsa_circ_177286,RMVar_hsa_circ_287907,RMVar_hsa_circ_372268,RMVar_hsa_circ_378253,RMVar_hsa_circ_339275,RMVar_hsa_circ_177292,RMVar_hsa_circ_177293,RMVar_hsa_circ_177294,RMVar_hsa_circ_177291 11937 RMVar_ID_11937 Human_SNP_ID_597751167 A-to-I Human chr16 - 23515202 23515202 23515202 TTCCTATCTGAGCCTCCCAAGTAGCTGAGACTACAGGGACTTGCACCACCACACCCAGCTGATAC TTCCTATCTGAGCCTCCCAAGTAGCTGAGACTGCAGGGACTTGCACCACCACACCCAGCTGATAC T C GGA2 Ensembl:ENSG00000103365 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1220184799 Functional Loss SNV dbSNP153 33..33 33 - - - 11938 RMVar_ID_11938 Human_SNP_ID_597751175 A-to-I Human chr16 - 23515267 23515267 23515267 GTTTTGTAGAGATGGTTGTCATTATGTTGCCCAGGCTGATCTTGAACCCCTGGGCTCAAGCAATC GTTTTGTAGAGATGGTTGTCATTATGTTGCCCGGGCTGATCTTGAACCCCTGGGCTCAAGCAATC T C GGA2 Ensembl:ENSG00000103365 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1363264167 Functional Loss SNV dbSNP153 33..33 33 - - - 11939 RMVar_ID_11939 Human_SNP_ID_597751180 A-to-I Human chr16 - 23515276 23515274 23515277 TATTTTTTGGTTTTGTAGAGATGGTTGTCATTATGTTGCCCAGGCTGATCTTGAACCCCTGGGCT TATTTTTTGGTTTTGTAGAGATGGTTGTCAT___GTTGCCCAGGCTGATCTTGAACCCCTGGGCT CATA C GGA2 Ensembl:ENSG00000103365 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1165877139 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_8429982 11940 RMVar_ID_11940 Human_SNP_ID_597751312 A-to-I Human chr16 - 23515907 23515907 23515907 TGAACCCAGGAGTTGGAGGCTGCAAGTGACCTATGATTGTGCCACTGCACTCCAGCCTGGGCAAC TGAACCCAGGAGTTGGAGGCTGCAAGTGACCTGTGATTGTGCCACTGCACTCCAGCCTGGGCAAC T C GGA2 Ensembl:ENSG00000103365 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1273654358 Functional Loss SNV dbSNP153 33..33 33 - - - 11941 RMVar_ID_11941 Human_SNP_ID_597751395 A-to-I Human chr16 - 23516211 23516211 23516211 ACCCAGGAGTTCGAGACCAGTCTGGGCAACATAGTAAGACCCCATCTTTACAAAAAATAGAAAAA ACCCAGGAGTTCGAGACCAGTCTGGGCAACATCGTAAGACCCCATCTTTACAAAAAATAGAAAAA T G GGA2 Ensembl:ENSG00000103365 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1478145366 Functional Loss SNV dbSNP153 33..33 33 - - - 11942 RMVar_ID_11942 Human_SNP_ID_597752430 A-to-I Human chr16 - 23520562 23520562 23520562 AGCTCTAACTCCTGGGCTCAAGAGATCCTCCTATCTCAGCCTCTTGAGTAGCTGGAATCACAGGT AGCTCTAACTCCTGGGCTCAAGAGATCCTCCTGTCTCAGCCTCTTGAGTAGCTGGAATCACAGGT T C GGA2 Ensembl:ENSG00000103365 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1294246420 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12694530 11943 RMVar_ID_11943 Human_SNP_ID_597752439 A-to-I Human chr16 - 23520609 23520609 23520609 GTTGCCTGCCCAGACTGGAGTGCAGTGGCACAATTATATTTCACTGTAGCTCTAACTCCTGGGCT GTTGCCTGCCCAGACTGGAGTGCAGTGGCACAGTTATATTTCACTGTAGCTCTAACTCCTGGGCT T C GGA2 Ensembl:ENSG00000103365 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1337582616 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8429988,Human_RBP_ID_9842192,Human_RBP_ID_25242881 11944 RMVar_ID_11944 Human_SNP_ID_597752505 A-to-I Human chr16 - 23520849 23520849 23520849 CAGAACGGGAGGTTGCAGTGAGCCAAGATCACACCATTGTACTCCAGCCTGGGGAACAGAGCGAC CAGAACGGGAGGTTGCAGTGAGCCAAGATCACGCCATTGTACTCCAGCCTGGGGAACAGAGCGAC T C EARS2,GGA2 Ensembl:ENSG00000103356,Ensembl:ENSG00000103365 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1453165075 Functional Loss SNV dbSNP153 33..33 33 - - - 11945 RMVar_ID_11945 Human_SNP_ID_597752657 A-to-I Human chr16 - 23521598 23521598 23521598 GCCAGGAGTTTGGAGACCAGCCTGGGCAACATAGTGAGATCCTGTCTCTACAAAAAATTTAAAAA GCCAGGAGTTTGGAGACCAGCCTGGGCAACATGGTGAGATCCTGTCTCTACAAAAAATTTAAAAA T C EARS2,GGA2 Ensembl:ENSG00000103356,Ensembl:ENSG00000103365 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1137263 Functional Loss SNV dbSNP153 33..33 33 - - - 11946 RMVar_ID_11946 Human_SNP_ID_597754924 A-to-I Human chr16 - 23530218 23530218 23530218 GGGAGGGTGAGATGGGAGGATCGCTTGAGCCTAGGAGGTCTAGGCTGTAGTGAGCCATGATCGTG GGGAGGGTGAGATGGGAGGATCGCTTGAGCCTGGGAGGTCTAGGCTGTAGTGAGCCATGATCGTG T C EARS2 Ensembl:ENSG00000103356 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs775301457 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39056,RMVar_hsa_circ_124162,RMVar_hsa_circ_88510,RMVar_hsa_circ_177309,RMVar_hsa_circ_66385,RMVar_hsa_circ_120418,RMVar_hsa_circ_177311,RMVar_hsa_circ_177312,RMVar_hsa_circ_330494,RMVar_hsa_circ_41505,RMVar_hsa_circ_304695,RMVar_hsa_circ_87428,RMVar_hsa_circ_177314 11947 RMVar_ID_11947 Human_SNP_ID_597754954 A-to-I Human chr16 - 23530325 23530325 23530325 GATTGCTTGTTGTTGCCTAGCCTGGACAACATAGCAAGACCCTGTCTCTACAAAAAACTAAAAAA GATTGCTTGTTGTTGCCTAGCCTGGACAACATCGCAAGACCCTGTCTCTACAAAAAACTAAAAAA T G EARS2 Ensembl:ENSG00000103356 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1237852095 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39056,RMVar_hsa_circ_124162,RMVar_hsa_circ_88510,RMVar_hsa_circ_177309,RMVar_hsa_circ_66385,RMVar_hsa_circ_120418,RMVar_hsa_circ_177311,RMVar_hsa_circ_177312,RMVar_hsa_circ_330494,RMVar_hsa_circ_41505,RMVar_hsa_circ_304695,RMVar_hsa_circ_87428,RMVar_hsa_circ_177314 11948 RMVar_ID_11948 Human_SNP_ID_597755639 A-to-I Human chr16 - 23532957 23532957 23532957 AAAATTAGCCAGGTGCGGTAGTATGTGCCTGTAGTCCCAGCTACTTGGAAGACAGGCTGGAGGAT AAAATTAGCCAGGTGCGGTAGTATGTGCCTGTCGTCCCAGCTACTTGGAAGACAGGCTGGAGGAT T G EARS2 Ensembl:ENSG00000103356 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041019934 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39056,RMVar_hsa_circ_124162,RMVar_hsa_circ_88510,RMVar_hsa_circ_177309,RMVar_hsa_circ_120418,RMVar_hsa_circ_177311,RMVar_hsa_circ_177312,RMVar_hsa_circ_330494,RMVar_hsa_circ_41505,RMVar_hsa_circ_87428,RMVar_hsa_circ_177314,RMVar_hsa_circ_282541,RMVar_hsa_circ_349171,RMVar_hsa_circ_177315 11949 RMVar_ID_11949 Human_SNP_ID_597761850 A-to-I Human chr16 - 23555441 23555441 23555441 GTCTGTCGTCCAGGCTGGAGTGCAGTGGTGCAATCTCGGCTCACTGCAACCTCAGCCTCCGGGGC GTCTGTCGTCCAGGCTGGAGTGCAGTGGTGCAGTCTCGGCTCACTGCAACCTCAGCCTCCGGGGC T C EARS2 Ensembl:ENSG00000103356 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1423891430 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124162,RMVar_hsa_circ_177311,RMVar_hsa_circ_110622,RMVar_hsa_circ_177320 11950 RMVar_ID_11950 Human_SNP_ID_597761930 A-to-I Human chr16 - 23555785 23555784 23555785 CCCAGCTACTCAGGAGGCTGAAAATCGTTTGAACCCAGGAGAAAGAGGTTGCAGTGAGCCGAGAT CCCAGCTACTCAGGAGGCTGAAAATCGTTTGA_CCCAGGAGAAAGAGGTTGCAGTGAGCCGAGAT GT G EARS2 Ensembl:ENSG00000103356 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1182457517 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_12694793 RMVar_hsa_circ_124162,RMVar_hsa_circ_177311,RMVar_hsa_circ_110622,RMVar_hsa_circ_177320 11951 RMVar_ID_11951 Human_SNP_ID_597765915 A-to-I Human chr16 + 23568325 23568325 23568325 GGGATTACAGGCTCACGCCACCACACCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCA GGGATTACAGGCTCACGCCACCACACCCAGCTGATTTTTGTATTTTTAGTAGAGATGGGGTTTCA A G UBFD1 Ensembl:ENSG00000103353 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1444094407 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99560,RMVar_hsa_circ_177321 11952 RMVar_ID_11952 Human_SNP_ID_597771596 A-to-I Human chr16 - 23588391 23588391 23588391 GGAATGCAATGGCGCAGGCTCGGCTCACTGCAACCTCTCCTCCCACATTCAAGCGATTCTCCTTC GGAATGCAATGGCGCAGGCTCGGCTCACTGCAGCCTCTCCTCCCACATTCAAGCGATTCTCCTTC T C NDUFAB1 Ensembl:ENSG00000004779 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs369946753 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12695532 RMVar_hsa_circ_123086,RMVar_hsa_circ_177331 11953 RMVar_ID_11953 Human_SNP_ID_597773287 A-to-I Human chr16 - 23594581 23594581 23594581 TTGGGATGCCGAGGCGGGCGGATCACGAGGTCAGGCGATCGAGACCATTCTGGCTAACACAGTGA TTGGGATGCCGAGGCGGGCGGATCACGAGGTCGGGCGATCGAGACCATTCTGGCTAACACAGTGA T C NDUFAB1 Ensembl:ENSG00000004779 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917199743 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123086,RMVar_hsa_circ_177331 11954 RMVar_ID_11954 Human_SNP_ID_597773414 A-to-I Human chr16 - 23595031 23595031 23595031 GGCCAGGTTGGTCTTGAACTCCCGACCTCGCAATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGA GGCCAGGTTGGTCTTGAACTCCCGACCTCGCAGTCCACCCGCCTCGGCCTCCCAAAGTGCTGGGA T C NDUFAB1 Ensembl:ENSG00000004779 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1014114538 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25198778 RMVar_hsa_circ_123086,RMVar_hsa_circ_177331 11955 RMVar_ID_11955 Human_SNP_ID_597773440 A-to-I Human chr16 - 23595139 23595139 23595139 CAAGCAATTCTCCTCCCTCAGCCCCCCCGAGTATTTGGGACTACAGGCGCCCGCCACCATGCCCG CAAGCAATTCTCCTCCCTCAGCCCCCCCGAGTGTTTGGGACTACAGGCGCCCGCCACCATGCCCG T C NDUFAB1 Ensembl:ENSG00000004779 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1281702023 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123086,RMVar_hsa_circ_177331 11956 RMVar_ID_11956 Human_SNP_ID_597773460 A-to-I Human chr16 - 23595165 23595165 23595165 TAACGGCAACCTCCGCCTCTCAGGTTCAAGCAATTCTCCTCCCTCAGCCCCCCCGAGTATTTGGG TAACGGCAACCTCCGCCTCTCAGGTTCAAGCAGTTCTCCTCCCTCAGCCCCCCCGAGTATTTGGG T C NDUFAB1 Ensembl:ENSG00000004779 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1029271623 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123086,RMVar_hsa_circ_177331 11957 RMVar_ID_11957 Human_SNP_ID_597773461 A-to-I Human chr16 - 23595165 23595165 23595165 TAACGGCAACCTCCGCCTCTCAGGTTCAAGCAATTCTCCTCCCTCAGCCCCCCCGAGTATTTGGG TAACGGCAACCTCCGCCTCTCAGGTTCAAGCACTTCTCCTCCCTCAGCCCCCCCGAGTATTTGGG T G NDUFAB1 Ensembl:ENSG00000004779 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1029271623 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123086,RMVar_hsa_circ_177331 11958 RMVar_ID_11958 Human_SNP_ID_597773462 A-to-I Human chr16 - 23595166 23595166 23595166 CTAACGGCAACCTCCGCCTCTCAGGTTCAAGCAATTCTCCTCCCTCAGCCCCCCCGAGTATTTGG CTAACGGCAACCTCCGCCTCTCAGGTTCAAGCGATTCTCCTCCCTCAGCCCCCCCGAGTATTTGG T C NDUFAB1 Ensembl:ENSG00000004779 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1202080642 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123086,RMVar_hsa_circ_177331 11959 RMVar_ID_11959 Human_SNP_ID_597776462 A-to-I Human chr16 - 23606353 23606353 23606353 TTGCCCAGGCTGGAGTGCAGTGGCACGATCTCAGCTCACTGCAACTCTGCCTCCCGGGTTCACAC TTGCCCAGGCTGGAGTGCAGTGGCACGATCTCGGCTCACTGCAACTCTGCCTCCCGGGTTCACAC T C PALB2 Ensembl:ENSG00000083093 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1015368998 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_177334,RMVar_hsa_circ_126804,RMVar_hsa_circ_177335,RMVar_hsa_circ_177336 11960 RMVar_ID_11960 Human_SNP_ID_597777394 A-to-I Human chr16 - 23609411 23609411 23609411 TCAGTTTTTTTCCCTTTTAGAGATAGGGTCTCACTCTCTCATTCAGGCTGTAGATCAGTGGCACC TCAGTTTTTTTCCCTTTTAGAGATAGGGTCTCCCTCTCTCATTCAGGCTGTAGATCAGTGGCACC T G PALB2 Ensembl:ENSG00000083093 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1425660228 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21224,RMVar_hsa_circ_177336,RMVar_hsa_circ_38459 11961 RMVar_ID_11961 Human_SNP_ID_597777817 A-to-I Human chr16 - 23610952 23610952 23610952 TCACTGCAACCTCCGCCTGCCAGGTTCAAGCAATTCTGTGCCTCAGCCTCCCAAGTAGCTGGGAT TCACTGCAACCTCCGCCTGCCAGGTTCAAGCAGTTCTGTGCCTCAGCCTCCCAAGTAGCTGGGAT T C PALB2 Ensembl:ENSG00000083093 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs879584534 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21224,RMVar_hsa_circ_177336,RMVar_hsa_circ_38459 11962 RMVar_ID_11962 Human_SNP_ID_597778535 A-to-I Human chr16 - 23613592 23613592 23613592 TTGCCCAGGCTGGAGTGCAATGGCGCGATCTCAGCTCACTGCAACCTCTGCCTTCTAGGTTCAAT TTGCCCAGGCTGGAGTGCAATGGCGCGATCTCGGCTCACTGCAACCTCTGCCTTCTAGGTTCAAT T C PALB2 Ensembl:ENSG00000083093 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1356687032 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21224,RMVar_hsa_circ_177336,RMVar_hsa_circ_38459 11963 RMVar_ID_11963 Human_SNP_ID_597786332 A-to-I Human chr16 - 23639298 23639298 23639298 GAACTCTTGACCTCAAATGATCCACCCACCTCAGCTTCCCCAAGTGTTGGGATTACAGGCGTGAG GAACTCTTGACCTCAAATGATCCACCCACCTCGGCTTCCCCAAGTGTTGGGATTACAGGCGTGAG T C PALB2 Ensembl:ENSG00000083093 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs939899982 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118534,RMVar_hsa_circ_177343 11964 RMVar_ID_11964 Human_SNP_ID_597786466 A-to-I Human chr16 - 23639671 23639671 23639671 GGATTACAGACGCCCAACACCACGCCGGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCTC GGATTACAGACGCCCAACACCACGCCGGGCTAGTTTTTGTATTTTTAGTAGAGACAGGGTTTCTC T C PALB2 Ensembl:ENSG00000083093 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs922470085 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118534,RMVar_hsa_circ_177343 11965 RMVar_ID_11965 Human_SNP_ID_597786467 A-to-I Human chr16 - 23639672 23639672 23639672 GGGATTACAGACGCCCAACACCACGCCGGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCT GGGATTACAGACGCCCAACACCACGCCGGGCTGATTTTTGTATTTTTAGTAGAGACAGGGTTTCT T C PALB2 Ensembl:ENSG00000083093 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs777401357 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118534,RMVar_hsa_circ_177343 11966 RMVar_ID_11966 Human_SNP_ID_597786504 A-to-I Human chr16 - 23639801 23639801 23639801 TTTGTTTGTTTTTGAGACAGACTCTCCGCTCTATCTCCCAGGCTGGAGTGCAGTGGCTCGATCTT TTTGTTTGTTTTTGAGACAGACTCTCCGCTCTGTCTCCCAGGCTGGAGTGCAGTGGCTCGATCTT T C PALB2 Ensembl:ENSG00000083093 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs574296292 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118534,RMVar_hsa_circ_177343 11967 RMVar_ID_11967 Human_SNP_ID_597786557 A-to-I Human chr16 - 23639991 23639991 23639991 GAGGCTCAGGCCTCAGAGGCTGATGCACGAGAATCGCTTGAACCAGGGGACGCTGAGGTTGCAGG GAGGCTCAGGCCTCAGAGGCTGATGCACGAGAGTCGCTTGAACCAGGGGACGCTGAGGTTGCAGG T C PALB2 Ensembl:ENSG00000083093 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs968018297 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118534,RMVar_hsa_circ_177343 11968 RMVar_ID_11968 Human_SNP_ID_597786593 A-to-I Human chr16 - 23640133 23640133 23640133 TAATCCCCGCACTTTGGGAGGCCGAGATGGGCAGATCGCTTGAGCTCAGAGTTTGAGACCAGCCT TAATCCCCGCACTTTGGGAGGCCGAGATGGGCGGATCGCTTGAGCTCAGAGTTTGAGACCAGCCT T C PALB2 Ensembl:ENSG00000083093 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1382347522 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118534,RMVar_hsa_circ_177343 11969 RMVar_ID_11969 Human_SNP_ID_597786676 A-to-I Human chr16 - 23640421 23640421 23640421 CGGCTCACTGCAACCTCCGCTTCCTGGGATCAAGCGACTCTCCTGCCTCAGCCTCCCGAGTAGCT CGGCTCACTGCAACCTCCGCTTCCTGGGATCAGGCGACTCTCCTGCCTCAGCCTCCCGAGTAGCT T C PALB2 Ensembl:ENSG00000083093 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs547262239 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118534,RMVar_hsa_circ_177343 11970 RMVar_ID_11970 Human_SNP_ID_597794766 A-to-I Human chr16 + 23672872 23672872 23672872 ATGTTTGGCCAGGCGCAGTGGCTCAAGCCTGTAATCCCATCACTTCGGGAGGCCGAGGTGGGCAG ATGTTTGGCCAGGCGCAGTGGCTCAAGCCTGTGATCCCATCACTTCGGGAGGCCGAGGTGGGCAG A G AC008870.1,DCTN5 Ensembl:ENSG00000260482,Ensembl:ENSG00000166847 lincRNA,Protein coding exon,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1137852 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8188357 Human_Splice_Rec_1692538 11971 RMVar_ID_11971 Human_SNP_ID_597794780 A-to-I Human chr16 + 23672924 23672924 23672924 CCGAGGTGGGCAGATCACGAGGTCAGGAGATCAAGACCATCCTGGCTAACACAGTGAAACCCCAT CCGAGGTGGGCAGATCACGAGGTCAGGAGATCGAGACCATCCTGGCTAACACAGTGAAACCCCAT A G AC008870.1,DCTN5 Ensembl:ENSG00000260482,Ensembl:ENSG00000166847 lincRNA,Protein coding exon,3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1286001059 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1692538 11972 RMVar_ID_11972 Human_SNP_ID_597794898 A-to-I Human chr16 + 23673304 23673304 23673304 TGCTTGTATTTGTTTATTTTTTAAATAGAGACAGGGTTTTACCATGTTGCCCAGACTAGTCTTGA TGCTTGTATTTGTTTATTTTTTAAATAGAGACGGGGTTTTACCATGTTGCCCAGACTAGTCTTGA A G AC008870.1,DCTN5 Ensembl:ENSG00000260482,Ensembl:ENSG00000166847 lincRNA,Protein coding exon,3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs574736626 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_47,Clinvar_Rec_48,Clinvar_Rec_49 11973 RMVar_ID_11973 Human_SNP_ID_597794903 A-to-I Human chr16 + 23673315 23673315 23673315 GTTTATTTTTTAAATAGAGACAGGGTTTTACCATGTTGCCCAGACTAGTCTTGAACTCCTGGGCT GTTTATTTTTTAAATAGAGACAGGGTTTTACCGTGTTGCCCAGACTAGTCTTGAACTCCTGGGCT A G AC008870.1,DCTN5 Ensembl:ENSG00000260482,Ensembl:ENSG00000166847 lincRNA,Protein coding exon,3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs1441503883 Functional Loss SNV dbSNP153 33..33 33 - - - 11974 RMVar_ID_11974 Human_SNP_ID_597849630 A-to-I Human chr16 + 23875729 23875703 23875730 ATATCACACATATATATGTATGTATATCACACATATATATGTATGTATATCACACATATATGTAT ATATCAC___________________________ATATATGTATGTATATCACACATATATGTAT CACATATATATGTATGTATATCACACAT C PRKCB Ensembl:ENSG00000166501 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1567298680 Functional Loss DEL dbSNP153 8..34 33 - - - RMVar_hsa_circ_78136,RMVar_hsa_circ_177361,RMVar_hsa_circ_90078,RMVar_hsa_circ_111066,RMVar_hsa_circ_177359,RMVar_hsa_circ_106212,RMVar_hsa_circ_177363,RMVar_hsa_circ_88051,RMVar_hsa_circ_177362,RMVar_hsa_circ_177360 11975 RMVar_ID_11975 Human_SNP_ID_597849646 A-to-I Human chr16 + 23875727 23875723 23875727 GTATATCACACATATATATGTATGTATATCACACATATATATGTATGTATATCACACATATATGT GTATATCACACATATATATGTATGTATAT____CATATATATGTATGTATATCACACATATATGT TCACA T PRKCB Ensembl:ENSG00000166501 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1211027198 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_78136,RMVar_hsa_circ_177361,RMVar_hsa_circ_90078,RMVar_hsa_circ_111066,RMVar_hsa_circ_177359,RMVar_hsa_circ_106212,RMVar_hsa_circ_177363,RMVar_hsa_circ_88051,RMVar_hsa_circ_177362,RMVar_hsa_circ_177360 11976 RMVar_ID_11976 Human_SNP_ID_597849647 A-to-I Human chr16 + 23875727 23875723 23875727 GTATATCACACATATATATGTATGTATATCACACATATATATGTATGTATATCACACATATATGT GTATATCACACATATATATGTATGTATATCA__CATATATATGTATGTATATCACACATATATGT TCACA TCA PRKCB Ensembl:ENSG00000166501 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1211027198 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_78136,RMVar_hsa_circ_177361,RMVar_hsa_circ_90078,RMVar_hsa_circ_111066,RMVar_hsa_circ_177359,RMVar_hsa_circ_106212,RMVar_hsa_circ_177363,RMVar_hsa_circ_88051,RMVar_hsa_circ_177362,RMVar_hsa_circ_177360 11977 RMVar_ID_11977 Human_SNP_ID_597849648 A-to-I Human chr16 + 23875729 23875726 23875730 ATATCACACATATATATGTATGTATATCACACATATATATGTATGTATATCACACATATATGTAT ATATCACACATATATATGTATGTATATCAC____ATATATGTATGTATATCACACATATATGTAT CACAT C PRKCB Ensembl:ENSG00000166501 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs71922460 Functional Loss DEL dbSNP153 31..34 33 - - - RMVar_hsa_circ_78136,RMVar_hsa_circ_177361,RMVar_hsa_circ_90078,RMVar_hsa_circ_111066,RMVar_hsa_circ_177359,RMVar_hsa_circ_106212,RMVar_hsa_circ_177363,RMVar_hsa_circ_88051,RMVar_hsa_circ_177362,RMVar_hsa_circ_177360 11978 RMVar_ID_11978 Human_SNP_ID_597849649 A-to-I Human chr16 + 23875729 23875728 23875730 ATATCACACATATATATGTATGTATATCACACATATATATGTATGTATATCACACATATATGTAT ATATCACACATATATATGTATGTATATCACAC__ATATATGTATGTATATCACACATATATGTAT CAT C PRKCB Ensembl:ENSG00000166501 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1343281471 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_78136,RMVar_hsa_circ_177361,RMVar_hsa_circ_90078,RMVar_hsa_circ_111066,RMVar_hsa_circ_177359,RMVar_hsa_circ_106212,RMVar_hsa_circ_177363,RMVar_hsa_circ_88051,RMVar_hsa_circ_177362,RMVar_hsa_circ_177360 11979 RMVar_ID_11979 Human_SNP_ID_597908407 A-to-I Human chr16 + 24110414 24110414 24110414 TTTTGTGGTTTTAGTACAGATGGGGTTTCACCATGTTGGCCAGGTTGTCTCGATCTCCTGACCTG TTTTGTGGTTTTAGTACAGATGGGGTTTCACCGTGTTGGCCAGGTTGTCTCGATCTCCTGACCTG A G PRKCB Ensembl:ENSG00000166501 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1284314030 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78136,RMVar_hsa_circ_177364,RMVar_hsa_circ_14545,RMVar_hsa_circ_90078,RMVar_hsa_circ_177359,RMVar_hsa_circ_106212,RMVar_hsa_circ_177363,RMVar_hsa_circ_177362,RMVar_hsa_circ_362070,RMVar_hsa_circ_370091,RMVar_hsa_circ_369822,RMVar_hsa_circ_314671,RMVar_hsa_circ_52032,RMVar_hsa_circ_177366,RMVar_hsa_circ_177365,RMVar_hsa_circ_19047,RMVar_hsa_circ_321154,RMVar_hsa_circ_332557,RMVar_hsa_circ_367243,RMVar_hsa_circ_177373,RMVar_hsa_circ_48345,RMVar_hsa_circ_177372,RMVar_hsa_circ_370696,RMVar_hsa_circ_316330,RMVar_hsa_circ_122793,RMVar_hsa_circ_177376,RMVar_hsa_circ_177377 11980 RMVar_ID_11980 Human_SNP_ID_597927562 A-to-I Human chr16 + 24187746 24187746 24187746 TGTCGCCCAGGCTAGAGTGCCGTGGAGTGATCATGGCTCACTGCAGCCTTGATCTCCCAGGCTCA TGTCGCCCAGGCTAGAGTGCCGTGGAGTGATCGTGGCTCACTGCAGCCTTGATCTCCCAGGCTCA A G PRKCB Ensembl:ENSG00000166501 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1169293531 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5153,RMVar_hsa_circ_177364,RMVar_hsa_circ_369822,RMVar_hsa_circ_79040,RMVar_hsa_circ_177378,RMVar_hsa_circ_264829,RMVar_hsa_circ_11390,RMVar_hsa_circ_276547,RMVar_hsa_circ_177384,RMVar_hsa_circ_270025,RMVar_hsa_circ_177386 11981 RMVar_ID_11981 Human_SNP_ID_598046273 A-to-I Human chr16 + 24645778 24645778 24645778 CAGCACTTTGGGAGGCCGAGGTGGGGAAGATCACTTGAGCTCAGGAGTTCGAGACCAACCTGGGA CAGCACTTTGGGAGGCCGAGGTGGGGAAGATCCCTTGAGCTCAGGAGTTCGAGACCAACCTGGGA A C TNRC6A Ensembl:ENSG00000090905 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs897476915 Functional Loss SNV dbSNP153 33..33 33 - - - 11982 RMVar_ID_11982 Human_SNP_ID_598046274 A-to-I Human chr16 + 24645778 24645778 24645778 CAGCACTTTGGGAGGCCGAGGTGGGGAAGATCACTTGAGCTCAGGAGTTCGAGACCAACCTGGGA CAGCACTTTGGGAGGCCGAGGTGGGGAAGATCGCTTGAGCTCAGGAGTTCGAGACCAACCTGGGA A G TNRC6A Ensembl:ENSG00000090905 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs897476915 Functional Loss SNV dbSNP153 33..33 33 - - - 11983 RMVar_ID_11983 Human_SNP_ID_598058085 A-to-I Human chr16 + 24690045 24690045 24690045 AAAAAAAAAAAAAAATTTTTTTTTTTTGAGATAGGGTCTCATTCTGTCACCCAGGCTGGAACACA AAAAAAAAAAAAAAATTTTTTTTTTTTGAGATGGGGTCTCATTCTGTCACCCAGGCTGGAACACA A G TNRC6A Ensembl:ENSG00000090905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1304221938 Functional Loss SNV dbSNP153 33..33 33 - - - 11984 RMVar_ID_11984 Human_SNP_ID_598069841 A-to-I Human chr16 + 24734100 24734100 24734100 GGGAGGCTGAGGTGGGAGGTTTGCTTGAGCCCAGCAGTTTGAGGCTTCAGTGAGCTGAGTTTGTG GGGAGGCTGAGGTGGGAGGTTTGCTTGAGCCCCGCAGTTTGAGGCTTCAGTGAGCTGAGTTTGTG A C TNRC6A Ensembl:ENSG00000090905 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs940570896 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26748,RMVar_hsa_circ_60725 11985 RMVar_ID_11985 Human_SNP_ID_598071214 A-to-I Human chr16 + 24739640 24739638 24739641 AGCTGGGATTACAGGCACCCACTACTATGCCCAACTAATTTTTGTATTTTTAATAGAGACAGAAT AGCTGGGATTACAGGCACCCACTACTATGCC___CTAATTTTTGTATTTTTAATAGAGACAGAAT CCAA C TNRC6A Ensembl:ENSG00000090905 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1369164130 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_26748,RMVar_hsa_circ_60725 11986 RMVar_ID_11986 Human_SNP_ID_598071215 A-to-I Human chr16 + 24739640 24739640 24739640 AGCTGGGATTACAGGCACCCACTACTATGCCCAACTAATTTTTGTATTTTTAATAGAGACAGAAT AGCTGGGATTACAGGCACCCACTACTATGCCCGACTAATTTTTGTATTTTTAATAGAGACAGAAT A G TNRC6A Ensembl:ENSG00000090905 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs550505587 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26748,RMVar_hsa_circ_60725 11987 RMVar_ID_11987 Human_SNP_ID_598071218 A-to-I Human chr16 + 24739659 24739659 24739659 CACTACTATGCCCAACTAATTTTTGTATTTTTAATAGAGACAGAATTTCACCATGTTGGCCAGGC CACTACTATGCCCAACTAATTTTTGTATTTTTTATAGAGACAGAATTTCACCATGTTGGCCAGGC A T TNRC6A Ensembl:ENSG00000090905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1056419280 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12698743 RMVar_hsa_circ_26748,RMVar_hsa_circ_60725 11988 RMVar_ID_11988 Human_SNP_ID_598071237 A-to-I Human chr16 + 24739753 24739753 24739753 CACCCGCCTCTGCCTCCCAAAGTGCTAGGATTACAGGCATGAGCCACCGCATGCAGCCTCTTTTC CACCCGCCTCTGCCTCCCAAAGTGCTAGGATTGCAGGCATGAGCCACCGCATGCAGCCTCTTTTC A G TNRC6A Ensembl:ENSG00000090905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1182248945 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12698747 RMVar_hsa_circ_26748,RMVar_hsa_circ_60725 11989 RMVar_ID_11989 Human_SNP_ID_598071728 A-to-I Human chr16 + 24741887 24741887 24741887 GGGACATGGTCTTGCTCTGTTGCCTAGGCTGGAATACAGTGGCGTGATCGTGGCTCACTGTAGCA GGGACATGGTCTTGCTCTGTTGCCTAGGCTGGCATACAGTGGCGTGATCGTGGCTCACTGTAGCA A C TNRC6A Ensembl:ENSG00000090905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1187051460 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26748,RMVar_hsa_circ_60725 11990 RMVar_ID_11990 Human_SNP_ID_598071753 A-to-I Human chr16 + 24741982 24741982 24741982 CTTCAGCCTCCTGAGGAGCTGGGACTACAGGCATGTGCCACTGTACCTGGCTAATTTTTTAATTT CTTCAGCCTCCTGAGGAGCTGGGACTACAGGCGTGTGCCACTGTACCTGGCTAATTTTTTAATTT A G TNRC6A Ensembl:ENSG00000090905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1430047338 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26748,RMVar_hsa_circ_60725 11991 RMVar_ID_11991 Human_SNP_ID_598071770 A-to-I Human chr16 + 24742101 24742101 24742101 CAAGTGATCCTACCACCTTGGCCTTCCAAAGCACTGGGATTACAGGTATGAGCCACCACACCTAG CAAGTGATCCTACCACCTTGGCCTTCCAAAGCGCTGGGATTACAGGTATGAGCCACCACACCTAG A G TNRC6A Ensembl:ENSG00000090905 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1234198643 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26748,RMVar_hsa_circ_60725 11992 RMVar_ID_11992 Human_SNP_ID_598072097 A-to-I Human chr16 + 24743589 24743589 24743589 CCAAGCAATCTGCCTTGGCCTCCCAAAGTGCTAGAATTGCAGGCATGAGCCACCTGCAGAGCTTT CCAAGCAATCTGCCTTGGCCTCCCAAAGTGCTGGAATTGCAGGCATGAGCCACCTGCAGAGCTTT A G TNRC6A Ensembl:ENSG00000090905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1429622483 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26748,RMVar_hsa_circ_60725 11993 RMVar_ID_11993 Human_SNP_ID_598072788 A-to-I Human chr16 + 24746279 24746279 24746279 ATTTTTTTCCTATAAAAAAAATCATGTTTCCTAGCTGAGTGCAGTGGCTCACCCCTGTAATCCCA ATTTTTTTCCTATAAAAAAAATCATGTTTCCTTGCTGAGTGCAGTGGCTCACCCCTGTAATCCCA A T TNRC6A Ensembl:ENSG00000090905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1421049483 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17123912 RMVar_hsa_circ_26748,RMVar_hsa_circ_60725 11994 RMVar_ID_11994 Human_SNP_ID_598072802 A-to-I Human chr16 + 24746332 24746332 24746332 CCTGTAATCCCAGTACTTTGGTAGGCCGAGGTAGGAGGATTGCTTGAGCCCAGGAGTTTGACACC CCTGTAATCCCAGTACTTTGGTAGGCCGAGGTGGGAGGATTGCTTGAGCCCAGGAGTTTGACACC A G TNRC6A Ensembl:ENSG00000090905 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1480879031 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17123912,Human_RBP_ID_22583999 RMVar_hsa_circ_26748,RMVar_hsa_circ_60725 11995 RMVar_ID_11995 Human_SNP_ID_598072938 A-to-I Human chr16 + 24746909 24746909 24746909 ATAGGCCCTTGAAATAGAGACAGACTCTCACTATGTTGCCCATTCTGTTCTCAAACTCCTGGCCT ATAGGCCCTTGAAATAGAGACAGACTCTCACTCTGTTGCCCATTCTGTTCTCAAACTCCTGGCCT A C TNRC6A Ensembl:ENSG00000090905 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs560433019 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26748,RMVar_hsa_circ_60725 11996 RMVar_ID_11996 Human_SNP_ID_598072939 A-to-I Human chr16 + 24746909 24746909 24746909 ATAGGCCCTTGAAATAGAGACAGACTCTCACTATGTTGCCCATTCTGTTCTCAAACTCCTGGCCT ATAGGCCCTTGAAATAGAGACAGACTCTCACTGTGTTGCCCATTCTGTTCTCAAACTCCTGGCCT A G TNRC6A Ensembl:ENSG00000090905 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs560433019 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26748,RMVar_hsa_circ_60725 11997 RMVar_ID_11997 Human_SNP_ID_598087006 A-to-I Human chr16 + 24801736 24801736 24801736 GGTCGCAAACTCCTGCCTGCCTCGGCCTCCCAAAGCGCTGAGATTACAAGTGTTAGCCACCGTGC GGTCGCAAACTCCTGCCTGCCTCGGCCTCCCAGAGCGCTGAGATTACAAGTGTTAGCCACCGTGC A G TNRC6A Ensembl:ENSG00000090905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs988096844 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23863,RMVar_hsa_circ_353789,RMVar_hsa_circ_265374,RMVar_hsa_circ_45427,RMVar_hsa_circ_269018,RMVar_hsa_circ_351298,RMVar_hsa_circ_177414,RMVar_hsa_circ_81031,RMVar_hsa_circ_67037,RMVar_hsa_circ_111076,RMVar_hsa_circ_177415,RMVar_hsa_circ_177416,RMVar_hsa_circ_101957,RMVar_hsa_circ_343459 11998 RMVar_ID_11998 Human_SNP_ID_598106032 A-to-I Human chr16 + 24872674 24872674 24872674 AGCTAGGACCACAGATGCAAGCCACCACACCCAGCTAATTTTTGCATTTTTTTTTTAGTAGAAAA AGCTAGGACCACAGATGCAAGCCACCACACCCGGCTAATTTTTGCATTTTTTTTTTAGTAGAAAA A G SLC5A11 Ensembl:ENSG00000158865 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1341688657 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_62359,RMVar_hsa_circ_342277,RMVar_hsa_circ_69443,RMVar_hsa_circ_4667,RMVar_hsa_circ_66357,RMVar_hsa_circ_177425,RMVar_hsa_circ_366251 11999 RMVar_ID_11999 Human_SNP_ID_598118898 A-to-I Human chr16 - 24920155 24920155 24920155 CGTGCCTGGCCGCATCCTGCTGGATATAGACAATGATACCGAGAGCACTGCCCTGTGAAGAAAGC CGTGCCTGGCCGCATCCTGCTGGATATAGACAGTGATACCGAGAGCACTGCCCTGTGAAGAAAGC T C ARHGAP17 Ensembl:ENSG00000140750 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs759941236 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_893413,Human_RBP_ID_1840295,Human_RBP_ID_5097411,Human_RBP_ID_6550143,Human_RBP_ID_8188657,Human_RBP_ID_17257050,Human_RBP_ID_17673267,Human_RBP_ID_17884417,Human_RBP_ID_19077453,Human_RBP_ID_21973529 Human_Splice_Rec_1693724 Human_miRNA_ID_1860653,Human_miRNA_ID_1861097,Human_miRNA_ID_1875155,Human_miRNA_ID_1875435 12000 RMVar_ID_12000 Human_SNP_ID_598119575 A-to-I Human chr16 - 24923281 24923281 24923281 TTCTCCTTTTTACAACAAACCAGAGTGTTTGTAAGACTGAAACAATGATCTTGGATAATGTCTTT TTCTCCTTTTTACAACAAACCAGAGTGTTTGTGAGACTGAAACAATGATCTTGGATAATGTCTTT T C ARHGAP17 Ensembl:ENSG00000140750 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1054324239 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12701342 12001 RMVar_ID_12001 Human_SNP_ID_598119817 A-to-I Human chr16 - 24924245 24924245 24924245 TAGAGGTGTTTAAAGAAAACCAGGTTCTTACAAGTGTCTTTCTAAAATAACCTTTATCTCTTTTT TAGAGGTGTTTAAAGAAAACCAGGTTCTTACAGGTGTCTTTCTAAAATAACCTTTATCTCTTTTT T C ARHGAP17 Ensembl:ENSG00000140750 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11864294 Functional Loss SNV dbSNP153 33..33 33 - - - 12002 RMVar_ID_12002 Human_SNP_ID_598119826 A-to-I Human chr16 - 24924300 24924300 24924300 AAGACCAGCCCTTCTTGGAATGCAAATAATATATAAATTCATAGCCAGAGACGTTTAGAGGTGTT AAGACCAGCCCTTCTTGGAATGCAAATAATATGTAAATTCATAGCCAGAGACGTTTAGAGGTGTT T C ARHGAP17 Ensembl:ENSG00000140750 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1029884173 Functional Loss SNV dbSNP153 33..33 33 - - - 12003 RMVar_ID_12003 Human_SNP_ID_598119827 A-to-I Human chr16 - 24924302 24924302 24924302 CAAAGACCAGCCCTTCTTGGAATGCAAATAATATATAAATTCATAGCCAGAGACGTTTAGAGGTG CAAAGACCAGCCCTTCTTGGAATGCAAATAATGTATAAATTCATAGCCAGAGACGTTTAGAGGTG T C ARHGAP17 Ensembl:ENSG00000140750 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1294393104 Functional Loss SNV dbSNP153 33..33 33 - - - 12004 RMVar_ID_12004 Human_SNP_ID_598119830 A-to-I Human chr16 - 24924308 24924308 24924308 TATGCTCAAAGACCAGCCCTTCTTGGAATGCAAATAATATATAAATTCATAGCCAGAGACGTTTA TATGCTCAAAGACCAGCCCTTCTTGGAATGCATATAATATATAAATTCATAGCCAGAGACGTTTA T A ARHGAP17 Ensembl:ENSG00000140750 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1317695663 Functional Loss SNV dbSNP153 33..33 33 - - - 12005 RMVar_ID_12005 Human_SNP_ID_598119998 A-to-I Human chr16 - 24925008 24925008 24925008 CCTTGGGTGAGGATCCTGAAAGTGAAGACATTATCTGAGGAAATAATGGTTTGGGTCTTAAACAC CCTTGGGTGAGGATCCTGAAAGTGAAGACATTTTCTGAGGAAATAATGGTTTGGGTCTTAAACAC T A ARHGAP17 Ensembl:ENSG00000140750 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs186879386 Functional Loss SNV dbSNP153 33..33 33 - - - 12006 RMVar_ID_12006 Human_SNP_ID_598119999 A-to-I Human chr16 - 24925008 24925008 24925008 CCTTGGGTGAGGATCCTGAAAGTGAAGACATTATCTGAGGAAATAATGGTTTGGGTCTTAAACAC CCTTGGGTGAGGATCCTGAAAGTGAAGACATTGTCTGAGGAAATAATGGTTTGGGTCTTAAACAC T C ARHGAP17 Ensembl:ENSG00000140750 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs186879386 Functional Loss SNV dbSNP153 33..33 33 - - - 12007 RMVar_ID_12007 Human_SNP_ID_598120025 A-to-I Human chr16 - 24925128 24925128 24925128 GTGATCCACTCACTTCTGCCTCCCAAAGTGCTAGGATTACAGGCATGAGCCACCGCACCTGGCCC GTGATCCACTCACTTCTGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCACCTGGCCC T C ARHGAP17 Ensembl:ENSG00000140750 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1181178758 Functional Loss SNV dbSNP153 33..33 33 - - - 12008 RMVar_ID_12008 Human_SNP_ID_598120068 A-to-I Human chr16 - 24925332 24925332 24925332 CTCTGTCACCCAGGCTGGAGTGCAGTGGTGCAATCTTGGCACACGGCAACCCCTGCCTTCCTGGT CTCTGTCACCCAGGCTGGAGTGCAGTGGTGCAGTCTTGGCACACGGCAACCCCTGCCTTCCTGGT T C ARHGAP17 Ensembl:ENSG00000140750 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs756916927 Functional Loss SNV dbSNP153 33..33 33 - - - 12009 RMVar_ID_12009 Human_SNP_ID_598120350 A-to-I Human chr16 - 24926377 24926377 24926377 GGGTGCCTGTAATCCCAGCTACTTGGGAGGCCAAGGCAGGAGAACTGCTTGAACCCAGGAGGTGG GGGTGCCTGTAATCCCAGCTACTTGGGAGGCCGAGGCAGGAGAACTGCTTGAACCCAGGAGGTGG T C ARHGAP17 Ensembl:ENSG00000140750 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1195569657 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25200372 12010 RMVar_ID_12010 Human_SNP_ID_598128664 A-to-I Human chr16 - 24960382 24960382 24960382 CGCCCCCACGCCTGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGC CGCCCCCACGCCTGGCTAATTTTTGTATTTTTGGTAGAGACGGGGTTTCACCATGTTGGCCAGGC T C ARHGAP17 Ensembl:ENSG00000140750 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1222453235 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4794,RMVar_hsa_circ_35711,RMVar_hsa_circ_39131,RMVar_hsa_circ_8533,RMVar_hsa_circ_34762,RMVar_hsa_circ_177428,RMVar_hsa_circ_65424,RMVar_hsa_circ_332123,RMVar_hsa_circ_366996,RMVar_hsa_circ_28362,RMVar_hsa_circ_11535,RMVar_hsa_circ_177430,RMVar_hsa_circ_329137,RMVar_hsa_circ_177431,RMVar_hsa_circ_55714,RMVar_hsa_circ_330307,RMVar_hsa_circ_338308 12011 RMVar_ID_12011 Human_SNP_ID_598131390 A-to-I Human chr16 - 24971492 24971492 24971492 AAAACCCTGTTTCTGCTAAAAGTACAGAAATTAGCTGGGTGTAAGTGGTGCATGCCCATAATCAC AAAACCCTGTTTCTGCTAAAAGTACAGAAATTGGCTGGGTGTAAGTGGTGCATGCCCATAATCAC T C ARHGAP17 Ensembl:ENSG00000140750 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs535412150 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18675876 RMVar_hsa_circ_50022,RMVar_hsa_circ_30387,RMVar_hsa_circ_27949,RMVar_hsa_circ_177432,RMVar_hsa_circ_374352,RMVar_hsa_circ_177435,RMVar_hsa_circ_34472 12012 RMVar_ID_12012 Human_SNP_ID_598133903 A-to-I Human chr16 - 24982212 24982212 24982212 TTTAGTAGAGATGAGGTTTTGCCATGTTGACCAGGCTGGTCTTGAACTTCTGACCTCAAGTGATC TTTAGTAGAGATGAGGTTTTGCCATGTTGACCCGGCTGGTCTTGAACTTCTGACCTCAAGTGATC T G ARHGAP17 Ensembl:ENSG00000140750 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910914701 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27949,RMVar_hsa_circ_112515,RMVar_hsa_circ_34472,RMVar_hsa_circ_177438 12013 RMVar_ID_12013 Human_SNP_ID_598139157 A-to-I Human chr16 - 25003399 25003399 25003399 GAAATCCTGTTTCTACTAAAAATGCCAAAATTAGCCAGGCATTGTGGTGCACACCTGTAATCCCA GAAATCCTGTTTCTACTAAAAATGCCAAAATTGGCCAGGCATTGTGGTGCACACCTGTAATCCCA T C ARHGAP17 Ensembl:ENSG00000140750 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs573982301 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27949,RMVar_hsa_circ_112515,RMVar_hsa_circ_34472,RMVar_hsa_circ_177438 12014 RMVar_ID_12014 Human_SNP_ID_598139257 A-to-I Human chr16 - 25003821 25003818 25003822 AAGTTGGTTCTTCAAAGCTTTTTTTTTTTTTGAGATGGATTCTTGCTCTGTCACCCAGGGTGGAG AAGTTGGTTCTTCAAAGCTTTTTTTTTTTTT____TGGATTCTTGCTCTGTCACCCAGGGTGGAG ATCTC A ARHGAP17 Ensembl:ENSG00000140750 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1368722226 Functional Loss DEL dbSNP153 32..35 33 - - - RMVar_hsa_circ_27949,RMVar_hsa_circ_112515,RMVar_hsa_circ_34472,RMVar_hsa_circ_177438 12015 RMVar_ID_12015 Human_SNP_ID_598158648 A-to-I Human chr16 + 25077088 25077087 25077088 GAGAGGCGGAGGTTGCAGTGAGCTGAGATTGCACCACTGCTCTCCAGCCTGGGTGACAGAGCAAA GAGAGGCGGAGGTTGCAGTGAGCTGAGATTGC_CCACTGCTCTCCAGCCTGGGTGACAGAGCAAA CA C LINC02175 Ensembl:ENSG00000262155 lincRNA intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1224999342 Functional Loss DEL dbSNP153 33..33 33 - - - 12016 RMVar_ID_12016 Human_SNP_ID_598158649 A-to-I Human chr16 + 25077088 25077088 25077088 GAGAGGCGGAGGTTGCAGTGAGCTGAGATTGCACCACTGCTCTCCAGCCTGGGTGACAGAGCAAA GAGAGGCGGAGGTTGCAGTGAGCTGAGATTGCGCCACTGCTCTCCAGCCTGGGTGACAGAGCAAA A G LINC02175 Ensembl:ENSG00000262155 lincRNA intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1304752255 Functional Loss SNV dbSNP153 33..33 33 - - - 12017 RMVar_ID_12017 Human_SNP_ID_598160898 A-to-I Human chr16 - 25086512 25086512 25086512 ATGGTGGCATGCACCTGTAATCACAGCTACTCAGGAGGTTGAGGCAGGAAAATCACTTGAACCTG ATGGTGGCATGCACCTGTAATCACAGCTACTCGGGAGGTTGAGGCAGGAAAATCACTTGAACCTG T C LCMT1-AS1 Ensembl:ENSG00000260448 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973272474 Functional Loss SNV dbSNP153 33..33 33 - - - 12018 RMVar_ID_12018 Human_SNP_ID_598173599 A-to-I Human chr16 + 25135940 25135940 25135940 TGACAAAACCCCATCTCTACAAAAAATAAAAAAATCAGCCAGGCATGGTGGTGCACACCTGTGGT TGACAAAACCCCATCTCTACAAAAAATAAAAACATCAGCCAGGCATGGTGGTGCACACCTGTGGT A C LCMT1 Ensembl:ENSG00000205629 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1033316899 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7575,RMVar_hsa_circ_300306,RMVar_hsa_circ_99021,RMVar_hsa_circ_177440,RMVar_hsa_circ_314702,RMVar_hsa_circ_115718,RMVar_hsa_circ_275554,RMVar_hsa_circ_68904,RMVar_hsa_circ_177441,RMVar_hsa_circ_177443,RMVar_hsa_circ_177442,RMVar_hsa_circ_349380 12019 RMVar_ID_12019 Human_SNP_ID_598180196 A-to-I Human chr16 + 25162544 25162544 25162544 CCAGGAGGCAGAGGTTGCAGTGAGCCAAGATCATGACATCGAACTGTAGCCTGGACAACAGAGCA CCAGGAGGCAGAGGTTGCAGTGAGCCAAGATCTTGACATCGAACTGTAGCCTGGACAACAGAGCA A T LCMT1 Ensembl:ENSG00000205629 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1440968211 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9823525 RMVar_hsa_circ_7575,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_339300,RMVar_hsa_circ_346317,RMVar_hsa_circ_52335,RMVar_hsa_circ_312672,RMVar_hsa_circ_315065,RMVar_hsa_circ_119792,RMVar_hsa_circ_177447,RMVar_hsa_circ_177448,RMVar_hsa_circ_177449,RMVar_hsa_circ_177451,RMVar_hsa_circ_286659,RMVar_hsa_circ_341896,RMVar_hsa_circ_277512,RMVar_hsa_circ_177450 12020 RMVar_ID_12020 Human_SNP_ID_598208023 A-to-I Human chr16 + 25263817 25263817 25263817 GCGATCGCGGCTCACTGTAACCTCCACCTCCCAGTTTTAAGTGAGTCTCCTGCTTCAGCCTCCCG GCGATCGCGGCTCACTGTAACCTCCACCTCCCGGTTTTAAGTGAGTCTCCTGCTTCAGCCTCCCG A G ZKSCAN2-DT,ZKSCAN2-DT:2,ZKSCAN2-DT:3,ZKSCAN2-DT:4,ZKSCAN2-DT:5 RNACentral:URS0000D57E1E,RNACentral:URS0000D5C5BA,RNACentral:URS0000D593D5,RNACentral:URS0000D58034,RNACentral:URS0000D5DA11 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,exon,intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs547957029 Functional Loss SNV dbSNP153 33..33 33 - - - 12021 RMVar_ID_12021 Human_SNP_ID_598384097 A-to-I Human chr16 + 25987161 25987161 25987161 TCACCTGAGGTCGGGAGTTCGAAACCAGCCTGACCAACATAGAGAAACCCCGTCTCTACTAAAAA TCACCTGAGGTCGGGAGTTCGAAACCAGCCTGCCCAACATAGAGAAACCCCGTCTCTACTAAAAA A C AC093516.1,HS3ST4 Ensembl:ENSG00000285882,Ensembl:ENSG00000182601 lincRNA,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1003182931 Functional Loss SNV dbSNP153 33..33 33 - - - 12022 RMVar_ID_12022 Human_SNP_ID_598384098 A-to-I Human chr16 + 25987161 25987161 25987161 TCACCTGAGGTCGGGAGTTCGAAACCAGCCTGACCAACATAGAGAAACCCCGTCTCTACTAAAAA TCACCTGAGGTCGGGAGTTCGAAACCAGCCTGTCCAACATAGAGAAACCCCGTCTCTACTAAAAA A T AC093516.1,HS3ST4 Ensembl:ENSG00000285882,Ensembl:ENSG00000182601 lincRNA,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1003182931 Functional Loss SNV dbSNP153 33..33 33 - - - 12023 RMVar_ID_12023 Human_SNP_ID_598384100 A-to-I Human chr16 + 25987167 25987167 25987167 GAGGTCGGGAGTTCGAAACCAGCCTGACCAACATAGAGAAACCCCGTCTCTACTAAAAATACAAA GAGGTCGGGAGTTCGAAACCAGCCTGACCAACGTAGAGAAACCCCGTCTCTACTAAAAATACAAA A G AC093516.1,HS3ST4 Ensembl:ENSG00000285882,Ensembl:ENSG00000182601 lincRNA,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs575178979 Functional Loss SNV dbSNP153 33..33 33 - - - 12024 RMVar_ID_12024 Human_SNP_ID_598715535 A-to-I Human chr16 - 27255961 27255961 27255961 AGAAAGGGTGTCCCTCCTGTCCCCAAAGGCAAACACTTCATGAGTGCATTACATCTTCTTCCCAG AGAAAGGGTGTCCCTCCTGTCCCCAAAGGCAAGCACTTCATGAGTGCATTACATCTTCTTCCCAG T C NSMCE1 Ensembl:ENSG00000169189 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1331308902 Functional Loss SNV dbSNP153 33..33 33 - - - 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 12025 RMVar_ID_12025 Human_SNP_ID_598761917 A-to-I Human chr16 + 27442505 27442505 27442505 CCTGCCTCAGCCTCCCGAGTAGATGGGACTACAGGCGCCCGCCACCACGCCCGGCTAATTTTTGT CCTGCCTCAGCCTCCCGAGTAGATGGGACTACGGGCGCCCGCCACCACGCCCGGCTAATTTTTGT A G IL21R Ensembl:ENSG00000103522 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs987859740 Functional Loss SNV dbSNP153 33..33 33 - - - 12026 RMVar_ID_12026 Human_SNP_ID_598762202 A-to-I Human chr16 + 27443637 27443637 27443637 AAACTCTGTTTCTACTAAAAATACAAAAAATTAGCCAGGCGTGGTGACATGCACCTGTAATCCAG AAACTCTGTTTCTACTAAAAATACAAAAAATTTGCCAGGCGTGGTGACATGCACCTGTAATCCAG A T IL21R Ensembl:ENSG00000103522 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1381105455 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18713,RMVar_hsa_circ_100813,RMVar_hsa_circ_177502 12027 RMVar_ID_12027 Human_SNP_ID_598762203 A-to-I Human chr16 + 27443641 27443641 27443641 TCTGTTTCTACTAAAAATACAAAAAATTAGCCAGGCGTGGTGACATGCACCTGTAATCCAGCTAT TCTGTTTCTACTAAAAATACAAAAAATTAGCCGGGCGTGGTGACATGCACCTGTAATCCAGCTAT A G IL21R Ensembl:ENSG00000103522 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs959195199 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18713,RMVar_hsa_circ_100813,RMVar_hsa_circ_177502 12028 RMVar_ID_12028 Human_SNP_ID_598764304 A-to-I Human chr16 + 27451620 27451620 27451620 GCTTGCCTATAGTCCCAGCTACTCGGGAGGCTAAGGTGGGAGGATCGCTGGAGCCCAGGAATTTG GCTTGCCTATAGTCCCAGCTACTCGGGAGGCTCAGGTGGGAGGATCGCTGGAGCCCAGGAATTTG A C IL21R Ensembl:ENSG00000103522 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1231925293 Functional Loss SNV dbSNP153 33..33 33 - - - 12029 RMVar_ID_12029 Human_SNP_ID_598764317 A-to-I Human chr16 + 27451674 27451674 27451674 CCAGGAATTTGAGGCTGCAGTGAGCTGTGATTACACCGTTGCACTCCAGCCTGGGTCACAGATCA CCAGGAATTTGAGGCTGCAGTGAGCTGTGATTGCACCGTTGCACTCCAGCCTGGGTCACAGATCA A G IL21R Ensembl:ENSG00000103522 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs3179917 Functional Loss SNV dbSNP153 33..33 33 - - - 12030 RMVar_ID_12030 Human_SNP_ID_598768035 A-to-I Human chr16 - 27465444 27465444 27465444 AAACCCCCAGGAAAACACCTGCAGCTTGGAGGAGTTTGTCCTCCAGCTGGAGCTGTCTGGGTATA AAACCCCCAGGAAAACACCTGCAGCTTGGAGGCGTTTGTCCTCCAGCTGGAGCTGTCTGGGTATA T G GTF3C1 Ensembl:ENSG00000077235 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350607506 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8806126,Human_RBP_ID_9285705,Human_RBP_ID_18411672,Human_RBP_ID_22760162 Human_Splice_Rec_1694674,Human_Splice_Rec_1694744 RMVar_hsa_circ_177505,RMVar_hsa_circ_88491,RMVar_hsa_circ_115330,RMVar_hsa_circ_127790,RMVar_hsa_circ_79127,RMVar_hsa_circ_83210,RMVar_hsa_circ_177507,RMVar_hsa_circ_177506,RMVar_hsa_circ_54776,RMVar_hsa_circ_177503,RMVar_hsa_circ_177504,RMVar_hsa_circ_177511,RMVar_hsa_circ_107651,RMVar_hsa_circ_67223,RMVar_hsa_circ_90704,RMVar_hsa_circ_177512 12031 RMVar_ID_12031 Human_SNP_ID_598771040 A-to-I Human chr16 - 27477531 27477531 27477531 GGAGGGCGCTGCCGGCGGATCACCTGAGGTCAAGAGTTCAAGGCCAGCCTGGCCAACATGGTGAA GGAGGGCGCTGCCGGCGGATCACCTGAGGTCAGGAGTTCAAGGCCAGCCTGGCCAACATGGTGAA T C GTF3C1 Ensembl:ENSG00000077235 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1183187074 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1670,RMVar_hsa_circ_177505,RMVar_hsa_circ_88491,RMVar_hsa_circ_115330,RMVar_hsa_circ_127790,RMVar_hsa_circ_79127,RMVar_hsa_circ_83210,RMVar_hsa_circ_177507,RMVar_hsa_circ_177506,RMVar_hsa_circ_54776,RMVar_hsa_circ_177503,RMVar_hsa_circ_177504,RMVar_hsa_circ_177511,RMVar_hsa_circ_107651,RMVar_hsa_circ_64854,RMVar_hsa_circ_90704,RMVar_hsa_circ_177512,RMVar_hsa_circ_26541 12032 RMVar_ID_12032 Human_SNP_ID_598771152 A-to-I Human chr16 - 27477965 27477965 27477965 GGGTTTTGCCGTGTTGGCCAGGCTGGTCTGGAACTCCTGGCCTCAAGTGATCTGCCCACCTTGGT GGGTTTTGCCGTGTTGGCCAGGCTGGTCTGGAGCTCCTGGCCTCAAGTGATCTGCCCACCTTGGT T C GTF3C1 Ensembl:ENSG00000077235 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1353619682 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1670,RMVar_hsa_circ_177505,RMVar_hsa_circ_88491,RMVar_hsa_circ_115330,RMVar_hsa_circ_127790,RMVar_hsa_circ_79127,RMVar_hsa_circ_83210,RMVar_hsa_circ_177507,RMVar_hsa_circ_177506,RMVar_hsa_circ_54776,RMVar_hsa_circ_177503,RMVar_hsa_circ_177504,RMVar_hsa_circ_177511,RMVar_hsa_circ_107651,RMVar_hsa_circ_64854,RMVar_hsa_circ_90704,RMVar_hsa_circ_177512,RMVar_hsa_circ_26541 12033 RMVar_ID_12033 Human_SNP_ID_598771169 A-to-I Human chr16 - 27478023 27478023 27478023 GAGATTACAGGCACCTGCCACCACACCCAGCTAATTTTTGTATTTTTTAGTAGAGACGGGGTTTT GAGATTACAGGCACCTGCCACCACACCCAGCTGATTTTTGTATTTTTTAGTAGAGACGGGGTTTT T C GTF3C1 Ensembl:ENSG00000077235 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1363829522 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1670,RMVar_hsa_circ_177505,RMVar_hsa_circ_88491,RMVar_hsa_circ_115330,RMVar_hsa_circ_127790,RMVar_hsa_circ_79127,RMVar_hsa_circ_83210,RMVar_hsa_circ_177507,RMVar_hsa_circ_177506,RMVar_hsa_circ_54776,RMVar_hsa_circ_177503,RMVar_hsa_circ_177504,RMVar_hsa_circ_177511,RMVar_hsa_circ_107651,RMVar_hsa_circ_64854,RMVar_hsa_circ_90704,RMVar_hsa_circ_177512,RMVar_hsa_circ_26541 12034 RMVar_ID_12034 Human_SNP_ID_598780785 A-to-I Human chr16 - 27515281 27515281 27515281 CCAACGCCTATAGCTAATTTTTTGTATTTGTTATGGAAATGAAGTCTTGCTCTGTTGCCCAGGCT CCAACGCCTATAGCTAATTTTTTGTATTTGTTGTGGAAATGAAGTCTTGCTCTGTTGCCCAGGCT T C GTF3C1 Ensembl:ENSG00000077235 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1385360185 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8430842,Human_RBP_ID_12706748 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_96112,RMVar_hsa_circ_177523,RMVar_hsa_circ_177525,RMVar_hsa_circ_177526,RMVar_hsa_circ_177524,RMVar_hsa_circ_266117,RMVar_hsa_circ_8292,RMVar_hsa_circ_59956,RMVar_hsa_circ_177529,RMVar_hsa_circ_113429,RMVar_hsa_circ_357263 12035 RMVar_ID_12035 Human_SNP_ID_598790496 A-to-I Human chr16 + 27553557 27553557 27553557 GTCCTGATGGTTGGGTTCAGTGGCTCACGCCTATAGTCCCACCGCTTTGGGAGGCCAAGACAAGA GTCCTGATGGTTGGGTTCAGTGGCTCACGCCTGTAGTCCCACCGCTTTGGGAGGCCAAGACAAGA A G KIAA0556 Ensembl:ENSG00000047578 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1159217753 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108706,RMVar_hsa_circ_177536 12036 RMVar_ID_12036 Human_SNP_ID_598790497 A-to-I Human chr16 + 27553559 27553559 27553559 CCTGATGGTTGGGTTCAGTGGCTCACGCCTATAGTCCCACCGCTTTGGGAGGCCAAGACAAGAGG CCTGATGGTTGGGTTCAGTGGCTCACGCCTATGGTCCCACCGCTTTGGGAGGCCAAGACAAGAGG A G KIAA0556 Ensembl:ENSG00000047578 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1453569237 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108706,RMVar_hsa_circ_177536 12037 RMVar_ID_12037 Human_SNP_ID_598834032 A-to-I Human chr16 + 27737196 27737196 27737196 GCCCAGGGGCTCAAGACCAGCCTGGACAACATAGTGAGACCCCGTCTCTACAAAAAAAAATTTAT GCCCAGGGGCTCAAGACCAGCCTGGACAACATGGTGAGACCCCGTCTCTACAAAAAAAAATTTAT A G KIAA0556 Ensembl:ENSG00000047578 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006145413 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6103,RMVar_hsa_circ_177541,RMVar_hsa_circ_89864,RMVar_hsa_circ_177547,RMVar_hsa_circ_120847,RMVar_hsa_circ_104779,RMVar_hsa_circ_177549,RMVar_hsa_circ_177552,RMVar_hsa_circ_6414,RMVar_hsa_circ_177553 12038 RMVar_ID_12038 Human_SNP_ID_598934037 A-to-I Human chr16 - 28136357 28136357 28136357 AAATTAGCCAGACCTAGTGGGTCATGCCTGTAATCCCAGCCACTCGGGAGGCTGAGGCATGAGAA AAATTAGCCAGACCTAGTGGGTCATGCCTGTAGTCCCAGCCACTCGGGAGGCTGAGGCATGAGAA T C XPO6 Ensembl:ENSG00000169180 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1258273111 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42265,RMVar_hsa_circ_81172,RMVar_hsa_circ_177561,RMVar_hsa_circ_103755,RMVar_hsa_circ_302811,RMVar_hsa_circ_323953,RMVar_hsa_circ_108269,RMVar_hsa_circ_177562,RMVar_hsa_circ_177564,RMVar_hsa_circ_177563,RMVar_hsa_circ_99501,RMVar_hsa_circ_177572,RMVar_hsa_circ_10119,RMVar_hsa_circ_110257,RMVar_hsa_circ_34243,RMVar_hsa_circ_106028,RMVar_hsa_circ_177576,RMVar_hsa_circ_114305,RMVar_hsa_circ_16550,RMVar_hsa_circ_177580,RMVar_hsa_circ_177579,RMVar_hsa_circ_107367,RMVar_hsa_circ_18503,RMVar_hsa_circ_44364,RMVar_hsa_circ_318775,RMVar_hsa_circ_375283,RMVar_hsa_circ_177583,RMVar_hsa_circ_177584,RMVar_hsa_circ_177589,RMVar_hsa_circ_318224,RMVar_hsa_circ_113397,RMVar_hsa_circ_177593,RMVar_hsa_circ_177594,RMVar_hsa_circ_346263,RMVar_hsa_circ_373888,RMVar_hsa_circ_375742,RMVar_hsa_circ_298486,RMVar_hsa_circ_10534,RMVar_hsa_circ_177595,RMVar_hsa_circ_177597,RMVar_hsa_circ_177596,RMVar_hsa_circ_271725,RMVar_hsa_circ_363728,RMVar_hsa_circ_341706,RMVar_hsa_circ_177600,RMVar_hsa_circ_177601,RMVar_hsa_circ_378642,RMVar_hsa_circ_288466,RMVar_hsa_circ_335315,RMVar_hsa_circ_9627,RMVar_hsa_circ_123592,RMVar_hsa_circ_177603,RMVar_hsa_circ_331374,RMVar_hsa_circ_103639,RMVar_hsa_circ_85744,RMVar_hsa_circ_177605,RMVar_hsa_circ_177606,RMVar_hsa_circ_102674,RMVar_hsa_circ_269576,RMVar_hsa_circ_177607,RMVar_hsa_circ_177608 12039 RMVar_ID_12039 Human_SNP_ID_598941500 A-to-I Human chr16 - 28168383 28168383 28168383 AGATTTTGGGGCCTAAGCGATCCTTCCACCTCAGCCTCCCCAGAAGCTGGGACTACAGGCATGCG AGATTTTGGGGCCTAAGCGATCCTTCCACCTCGGCCTCCCCAGAAGCTGGGACTACAGGCATGCG T C XPO6 Ensembl:ENSG00000169180 Protein coding intron GSE38233;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,32596459 RNA-Seq:(High) rs774503072 Functional Loss SNV dbSNP153 33..33 33 - - - 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 12040 RMVar_ID_12040 Human_SNP_ID_598941584 A-to-I Human chr16 - 28168670 28168670 28168670 TTGAGCTCAGGAGTTTGAGGCTGCAGTGACCTATGATCGTACCACTGCACTCCAGCCTGGGTGAC TTGAGCTCAGGAGTTTGAGGCTGCAGTGACCTGTGATCGTACCACTGCACTCCAGCCTGGGTGAC T C XPO6 Ensembl:ENSG00000169180 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs776363353 Functional Loss SNV dbSNP153 33..33 33 - - - 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 12041 RMVar_ID_12041 Human_SNP_ID_598941636 A-to-I Human chr16 - 28168823 28168823 28168823 ATCACTTGAGCCCAGGAGTTTGAGACCAGACTAGGCAACATATTGAGACCCCCATTTCTGGAAAA ATCACTTGAGCCCAGGAGTTTGAGACCAGACTGGGCAACATATTGAGACCCCCATTTCTGGAAAA T C XPO6 Ensembl:ENSG00000169180 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs935968876 Functional Loss SNV dbSNP153 33..33 33 - - - 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 12042 RMVar_ID_12042 Human_SNP_ID_598941652 A-to-I Human chr16 - 28168903 28168903 28168903 CCATTGATTTAAAGTAAACTTGGGTTAGTGCAATGGCTCACACCTGTAATCCCAGTGCTTTGGGA CCATTGATTTAAAGTAAACTTGGGTTAGTGCAGTGGCTCACACCTGTAATCCCAGTGCTTTGGGA T C XPO6 Ensembl:ENSG00000169180 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1261824709 Functional Loss SNV dbSNP153 33..33 33 - - - 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 12043 RMVar_ID_12043 Human_SNP_ID_598948998 A-to-I Human chr16 - 28199704 28199704 28199704 CCATTAGCCAGGTGTGGTGGTGGGTGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAA CCATTAGCCAGGTGTGGTGGTGGGTGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAA T C XPO6 Ensembl:ENSG00000169180 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1165755236 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110257,RMVar_hsa_circ_177576,RMVar_hsa_circ_113397,RMVar_hsa_circ_177594,RMVar_hsa_circ_123592,RMVar_hsa_circ_177606,RMVar_hsa_circ_90873,RMVar_hsa_circ_177612,RMVar_hsa_circ_79990,RMVar_hsa_circ_177620,RMVar_hsa_circ_10645 12044 RMVar_ID_12044 Human_SNP_ID_598990638 A-to-I Human chr16 - 28361634 28361634 28361634 TCACTGCAACCTCTGTCTCCCGGGTTCAAGCAATTCCTCTGCCTCAGCCTCTGAGTAGCTGGGAC TCACTGCAACCTCTGTCTCCCGGGTTCAAGCAGTTCCTCTGCCTCAGCCTCTGAGTAGCTGGGAC T C NPIPB6 Ensembl:ENSG00000198156 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1338353994 Functional Loss SNV dbSNP153 33..33 33 - - - 12045 RMVar_ID_12045 Human_SNP_ID_598992505 A-to-I Human chr16 - 28369808 28369808 28369808 TTGCTCTGTCACCCAGGCTGGATTGTAGTGGCACGATCTCAGCTCACTGAAACCTTCGCCTCCTG TTGCTCTGTCACCCAGGCTGGATTGTAGTGGCGCGATCTCAGCTCACTGAAACCTTCGCCTCCTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1353908570 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12711750,Human_RBP_ID_25203391 12046 RMVar_ID_12046 Human_SNP_ID_599011460 A-to-I Human chr16 - 28473006 28473006 28473006 TTGAGCCTAGGAATTCGAGGCTGCAGTGAGCTATGATCATACCACTGCACCCCAATGTGGGCACA TTGAGCCTAGGAATTCGAGGCTGCAGTGAGCTGTGATCATACCACTGCACCCCAATGTGGGCACA T C AC138894.1 Ensembl:ENSG00000261832 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs750982561 Functional Loss SNV dbSNP153 33..33 33 - - - 12047 RMVar_ID_12047 Human_SNP_ID_599011965 A-to-I Human chr16 - 28475134 28475134 28475134 GGGGTCCTCCTGCCTCAGCCTCCTGAGTATCTAAGACTGCAGGCACGCACCACCATACCTGGCTA GGGGTCCTCCTGCCTCAGCCTCCTGAGTATCTGAGACTGCAGGCACGCACCACCATACCTGGCTA T C AC138894.1,CLN3 Ensembl:ENSG00000261832,Ensembl:ENSG00000188603 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910966071 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12711788 12048 RMVar_ID_12048 Human_SNP_ID_599013038 A-to-I Human chr16 - 28479011 28479011 28479011 GGCTTCCTGGCCAGGTGCGGTGGCTCCTGCCTATAATCCCAGCACTTTGGGAGGCTGAGGCAGGG GGCTTCCTGGCCAGGTGCGGTGGCTCCTGCCTTTAATCCCAGCACTTTGGGAGGCTGAGGCAGGG T A AC138894.1,CLN3 Ensembl:ENSG00000261832,Ensembl:ENSG00000188603 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1398281113 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86047,RMVar_hsa_circ_96211,RMVar_hsa_circ_102935,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_177634,RMVar_hsa_circ_177640,RMVar_hsa_circ_8475,RMVar_hsa_circ_106815 12049 RMVar_ID_12049 Human_SNP_ID_599013807 A-to-I Human chr16 - 28481775 28481775 28481775 GCCATATTGGCTGGTCTTGAACTCTTGACCTCAGGTGATCTGCCGGCCTCAGCCTCCCAAAGTGC GCCATATTGGCTGGTCTTGAACTCTTGACCTCTGGTGATCTGCCGGCCTCAGCCTCCCAAAGTGC T A AC138894.1,CLN3 Ensembl:ENSG00000261832,Ensembl:ENSG00000188603 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1242235685 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86047,RMVar_hsa_circ_96211,RMVar_hsa_circ_102935,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_177634,RMVar_hsa_circ_177640,RMVar_hsa_circ_8475,RMVar_hsa_circ_106815 12050 RMVar_ID_12050 Human_SNP_ID_599013808 A-to-I Human chr16 - 28481775 28481775 28481775 GCCATATTGGCTGGTCTTGAACTCTTGACCTCAGGTGATCTGCCGGCCTCAGCCTCCCAAAGTGC GCCATATTGGCTGGTCTTGAACTCTTGACCTCGGGTGATCTGCCGGCCTCAGCCTCCCAAAGTGC T C AC138894.1,CLN3 Ensembl:ENSG00000261832,Ensembl:ENSG00000188603 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1242235685 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86047,RMVar_hsa_circ_96211,RMVar_hsa_circ_102935,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_177634,RMVar_hsa_circ_177640,RMVar_hsa_circ_8475,RMVar_hsa_circ_106815 12051 RMVar_ID_12051 Human_SNP_ID_599014878 A-to-I Human chr16 - 28485215 28485215 28485215 ACTTTGGCCGGGCATGGTGGCTCACATCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGCA ACTTTGGCCGGGCATGGTGGCTCACATCTGTAGTCCCAGCACTTTGGGAGGCCGAGGCGGGCGCA T C AC138894.1,CLN3 Ensembl:ENSG00000261832,Ensembl:ENSG00000188603 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215069299 Functional Loss SNV dbSNP153 33..33 33 - - - 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_110227,RMVar_hsa_circ_177641,RMVar_hsa_circ_177642,RMVar_hsa_circ_318299,RMVar_hsa_circ_177643 12052 RMVar_ID_12052 Human_SNP_ID_599015155 A-to-I Human chr16 - 28486122 28486122 28486122 GTGGTGGCGGGTGCCTGTAGTCCCAACTACTCAGGAGGCTAAGGCAGGAGAATCGCTTGAACCCC GTGGTGGCGGGTGCCTGTAGTCCCAACTACTCTGGAGGCTAAGGCAGGAGAATCGCTTGAACCCC T A AC138894.1,CLN3 Ensembl:ENSG00000261832,Ensembl:ENSG00000188603 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs923533328 Functional Loss SNV dbSNP153 33..33 33 - - - 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_110227,RMVar_hsa_circ_177641,RMVar_hsa_circ_177642,RMVar_hsa_circ_318299,RMVar_hsa_circ_177643 12053 RMVar_ID_12053 Human_SNP_ID_599027821 A-to-I Human chr16 - 28530522 28530522 28530522 TGTGCCTGTAGTCCTAGCTACTCAGGAGGCTTAGGTGGGAGGATCGTTTGAGCCCAGGAGTTTGA TGTGCCTGTAGTCCTAGCTACTCAGGAGGCTTCGGTGGGAGGATCGTTTGAGCCCAGGAGTTTGA T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1281796914 Functional Loss SNV dbSNP153 33..33 33 - - - 12054 RMVar_ID_12054 Human_SNP_ID_599028176 A-to-I Human chr16 - 28531974 28531974 28531974 CACTGCAGCCTTGACCTCCTGGGCTAATTTTTAAATTTTTCGTAGAGATGAAGTCTCGCTGCTAT CACTGCAGCCTTGACCTCCTGGGCTAATTTTTTAATTTTTCGTAGAGATGAAGTCTCGCTGCTAT T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1294936780 Functional Loss SNV dbSNP153 33..33 33 - - - 12055 RMVar_ID_12055 Human_SNP_ID_599029623 A-to-I Human chr16 - 28536591 28536591 28536591 ACAGCAGTTTAGGAGGCCGAAGTGGGAGGATTACTTGAGCCTAGGAGTTTGAGACCAGCCTGAGC ACAGCAGTTTAGGAGGCCGAAGTGGGAGGATTGCTTGAGCCTAGGAGTTTGAGACCAGCCTGAGC T C NUPR1 Ensembl:ENSG00000176046 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1204277352 Functional Loss SNV dbSNP153 33..33 33 - - - 12056 RMVar_ID_12056 Human_SNP_ID_599034685 A-to-I Human chr16 + 28555120 28555120 28555120 CTTAAGCAGTCCTCCTAACCAAAGCCTCCCCAAATGCTGGAATTACAGGCATGAGCCACCGCAAT CTTAAGCAGTCCTCCTAACCAAAGCCTCCCCAGATGCTGGAATTACAGGCATGAGCCACCGCAAT A G SGF29 Ensembl:ENSG00000176476 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1452565452 Functional Loss SNV dbSNP153 33..33 33 - - - 12057 RMVar_ID_12057 Human_SNP_ID_599038285 A-to-I Human chr16 + 28567248 28567248 28567248 ATAGAGATGTTCAACCAGTGAGTGAGTATCTTAGTTCATTTGGGTTGCTGTAACAAAATACCTTA ATAGAGATGTTCAACCAGTGAGTGAGTATCTTTGTTCATTTGGGTTGCTGTAACAAAATACCTTA A T SGF29 Ensembl:ENSG00000176476 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1489018876 Functional Loss SNV dbSNP153 33..33 33 - - - 12058 RMVar_ID_12058 Human_SNP_ID_599044722 A-to-I Human chr16 - 28592890 28592889 28592890 CTCCTGCCTCAGCCTCCTGAGTAGCTGAGATTACAGATGCACACTACCATGCCTGGCTAATTTTT CTCCTGCCTCAGCCTCCTGAGTAGCTGAGATT_CAGATGCACACTACCATGCCTGGCTAATTTTT GT G SULT1A2 Ensembl:ENSG00000197165 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1026730492 Functional Loss DEL dbSNP153 33..33 33 - - - 12059 RMVar_ID_12059 Human_SNP_ID_599045331 A-to-I Human chr16 - 28594264 28594264 28594264 TGGTGGCATAGCGCTATAGTCCCAGCTACTCAAAAGTCTAAGGTTGGAGGATTGCTTGAGCCTGG TGGTGGCATAGCGCTATAGTCCCAGCTACTCAGAAGTCTAAGGTTGGAGGATTGCTTGAGCCTGG T C SULT1A2 Ensembl:ENSG00000197165 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs908491571 Functional Loss SNV dbSNP153 33..33 33 - - - 12060 RMVar_ID_12060 Human_SNP_ID_599048561 A-to-I Human chr16 - 28605727 28605727 28605727 GAATAAAATATGAATTGAGGGCCCGGGACGGTAGGTCATGTCTGTAATCCCAGCAATTTGGAGGC GAATAAAATATGAATTGAGGGCCCGGGACGGTCGGTCATGTCTGTAATCCCAGCAATTTGGAGGC T G SULT1A1 Ensembl:ENSG00000196502 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1010701089 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_46387,Human_RBP_ID_4360641,Human_RBP_ID_17652954,Human_RBP_ID_17874742 12061 RMVar_ID_12061 Human_SNP_ID_599052045 A-to-I Human chr16 - 28616451 28616451 28616451 AAACCCAGTCTCTACTAAAAATACAAAAAATTAGCCAGGCATGGTGGCGCACGCCTGTAATCCCA AAACCCAGTCTCTACTAAAAATACAAAAAATTGGCCAGGCATGGTGGCGCACGCCTGTAATCCCA T C SULT1A1 Ensembl:ENSG00000196502 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1030953603 Functional Loss SNV dbSNP153 33..33 33 - - - 12062 RMVar_ID_12062 Human_SNP_ID_599052752 A-to-I Human chr16 - 28619141 28619141 28619141 GGGCACGGTGGTGTATGTCTGTAATCCCAGCTACTCAGTAGGCTGAGGCAGGAGAATCACTTGAA GGGCACGGTGGTGTATGTCTGTAATCCCAGCTGCTCAGTAGGCTGAGGCAGGAGAATCACTTGAA T C SULT1A1 Ensembl:ENSG00000196502 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264502348 Functional Loss SNV dbSNP153 33..33 33 - - - 12063 RMVar_ID_12063 Human_SNP_ID_599052848 A-to-I Human chr16 - 28619598 28619598 28619598 CTCCCACCTCATCCTTCTGAGTAGCTGAGACTACAGGCATGTGCCACCACACCCAGCTAATTATT CTCCCACCTCATCCTTCTGAGTAGCTGAGACTGCAGGCATGTGCCACCACACCCAGCTAATTATT T C SULT1A1 Ensembl:ENSG00000196502 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1441383835 Functional Loss SNV dbSNP153 33..33 33 - - - 12064 RMVar_ID_12064 Human_SNP_ID_599094157 A-to-I Human chr16 + 28828325 28828325 28828325 TTAACAGTTGCAGGCCGGGCGCGGTGGCTCACACCAGTAATCCCAGCACTTTGGGAGGCCAAGGC TTAACAGTTGCAGGCCGGGCGCGGTGGCTCACCCCAGTAATCCCAGCACTTTGGGAGGCCAAGGC A C ATXN2L Ensembl:ENSG00000168488 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1036725208 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4350,RMVar_hsa_circ_114503,RMVar_hsa_circ_369517,RMVar_hsa_circ_60886,RMVar_hsa_circ_177669,RMVar_hsa_circ_177670,RMVar_hsa_circ_4633,RMVar_hsa_circ_51683 12065 RMVar_ID_12065 Human_SNP_ID_599094158 A-to-I Human chr16 + 28828325 28828325 28828325 TTAACAGTTGCAGGCCGGGCGCGGTGGCTCACACCAGTAATCCCAGCACTTTGGGAGGCCAAGGC TTAACAGTTGCAGGCCGGGCGCGGTGGCTCACGCCAGTAATCCCAGCACTTTGGGAGGCCAAGGC A G ATXN2L Ensembl:ENSG00000168488 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1036725208 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4350,RMVar_hsa_circ_114503,RMVar_hsa_circ_369517,RMVar_hsa_circ_60886,RMVar_hsa_circ_177669,RMVar_hsa_circ_177670,RMVar_hsa_circ_4633,RMVar_hsa_circ_51683 12066 RMVar_ID_12066 Human_SNP_ID_599094186 A-to-I Human chr16 + 28828416 28828416 28828416 TGGAACTAGCCTGACCAACGTGGAGAAGCCCCATCTCTACTAAAAATACAAAATTAGCTGGGCGT TGGAACTAGCCTGACCAACGTGGAGAAGCCCCGTCTCTACTAAAAATACAAAATTAGCTGGGCGT A G ATXN2L Ensembl:ENSG00000168488 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1437071170 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12712195 RMVar_hsa_circ_4350,RMVar_hsa_circ_114503,RMVar_hsa_circ_369517,RMVar_hsa_circ_60886,RMVar_hsa_circ_177669,RMVar_hsa_circ_177670,RMVar_hsa_circ_4633,RMVar_hsa_circ_51683 12067 RMVar_ID_12067 Human_SNP_ID_599094193 A-to-I Human chr16 + 28828439 28828439 28828439 AGAAGCCCCATCTCTACTAAAAATACAAAATTAGCTGGGCGTGGTGGCACATGCCCGTAATCCCA AGAAGCCCCATCTCTACTAAAAATACAAAATTTGCTGGGCGTGGTGGCACATGCCCGTAATCCCA A T ATXN2L Ensembl:ENSG00000168488 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs939954156 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4350,RMVar_hsa_circ_114503,RMVar_hsa_circ_369517,RMVar_hsa_circ_60886,RMVar_hsa_circ_177669,RMVar_hsa_circ_177670,RMVar_hsa_circ_4633,RMVar_hsa_circ_51683 12068 RMVar_ID_12068 Human_SNP_ID_599094204 A-to-I Human chr16 + 28828465 28828465 28828465 AAAATTAGCTGGGCGTGGTGGCACATGCCCGTAATCCCAGCTACTCGTGAGGTTGAGGCAGGAGA AAAATTAGCTGGGCGTGGTGGCACATGCCCGTGATCCCAGCTACTCGTGAGGTTGAGGCAGGAGA A G ATXN2L Ensembl:ENSG00000168488 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs754125505 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4350,RMVar_hsa_circ_114503,RMVar_hsa_circ_369517,RMVar_hsa_circ_60886,RMVar_hsa_circ_177669,RMVar_hsa_circ_177670,RMVar_hsa_circ_4633,RMVar_hsa_circ_51683 12069 RMVar_ID_12069 Human_SNP_ID_599094206 A-to-I Human chr16 + 28828475 28828475 28828475 GGGCGTGGTGGCACATGCCCGTAATCCCAGCTACTCGTGAGGTTGAGGCAGGAGAATCGCTTGAA GGGCGTGGTGGCACATGCCCGTAATCCCAGCTGCTCGTGAGGTTGAGGCAGGAGAATCGCTTGAA A G ATXN2L Ensembl:ENSG00000168488 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1021782483 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4350,RMVar_hsa_circ_114503,RMVar_hsa_circ_369517,RMVar_hsa_circ_60886,RMVar_hsa_circ_177669,RMVar_hsa_circ_177670,RMVar_hsa_circ_4633,RMVar_hsa_circ_51683 12070 RMVar_ID_12070 Human_SNP_ID_599094445 A-to-I Human chr16 + 28829237 28829237 28829237 GTTGCCCAGTCTGGCCTTAAACTCCTGGCCTCAGGAGAGCCTCCTGCCTCAGCTTCCCAAAGTAC GTTGCCCAGTCTGGCCTTAAACTCCTGGCCTCTGGAGAGCCTCCTGCCTCAGCTTCCCAAAGTAC A T ATXN2L Ensembl:ENSG00000168488 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1012550694 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6506211,Human_RBP_ID_25203588 RMVar_hsa_circ_4350,RMVar_hsa_circ_114503,RMVar_hsa_circ_369517,RMVar_hsa_circ_60886,RMVar_hsa_circ_177669,RMVar_hsa_circ_177670,RMVar_hsa_circ_4633,RMVar_hsa_circ_51683 12071 RMVar_ID_12071 Human_SNP_ID_599095198 A-to-I Human chr16 + 28831469 28831469 28831469 CCTGTCTCAGCCTCCCAAGTAGCTGGGATTACAGGCACCCACCACCACGGCTGGCTAATTTTTTT CCTGTCTCAGCCTCCCAAGTAGCTGGGATTACGGGCACCCACCACCACGGCTGGCTAATTTTTTT A G ATXN2L Ensembl:ENSG00000168488 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1264620910 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4350,RMVar_hsa_circ_369517,RMVar_hsa_circ_177670,RMVar_hsa_circ_49675 12072 RMVar_ID_12072 Human_SNP_ID_599099682 A-to-I Human chr16 - 28844336 28844336 28844336 GGGGTCCCTGATATCCTGTCTTATTCCCTCCCAGGCCGTGGCACCGTGGTGACAGGTACACTAGA GGGGTCCCTGATATCCTGTCTTATTCCCTCCCTGGCCGTGGCACCGTGGTGACAGGTACACTAGA T A TUFM Ensembl:ENSG00000178952 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs879127036 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5355728,Human_RBP_ID_22651881 RMVar_hsa_circ_4056,RMVar_hsa_circ_89568,RMVar_hsa_circ_177677 12073 RMVar_ID_12073 Human_SNP_ID_599101266 A-to-I Human chr16 + 28849358 28849358 28849358 GGCCCAAGCCGTCTGCCCACCTTGGCCTCTCAAAATGCTGGGATTACAGGCATGAGCCACTGTGC GGCCCAAGCCGTCTGCCCACCTTGGCCTCTCAGAATGCTGGGATTACAGGCATGAGCCACTGTGC A G SH2B1 Ensembl:ENSG00000178188 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1567456936 Functional Loss SNV dbSNP153 33..33 33 - - - 12074 RMVar_ID_12074 Human_SNP_ID_599120942 A-to-I Human chr16 - 28909760 28909760 28909760 TCGGCCTCCCAAAGTGCTGGGATTACAGGCGTAAGCCACTGAGCCCGGCCTCCTGTTTTTTTTTT TCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGAGCCCGGCCTCCTGTTTTTTTTTT T C RABEP2 Ensembl:ENSG00000177548 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1344256920 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_177688,RMVar_hsa_circ_49471 12075 RMVar_ID_12075 Human_SNP_ID_599121135 A-to-I Human chr16 - 28910420 28910420 28910420 CAAAAATTAGCCGGGCATGGTGGTGGGCGCCTATAATCCCAGCTACTTGGCTGGGCAGGATAATC CAAAAATTAGCCGGGCATGGTGGTGGGCGCCTGTAATCCCAGCTACTTGGCTGGGCAGGATAATC T C RABEP2 Ensembl:ENSG00000177548 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs964200792 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_177688,RMVar_hsa_circ_49471 12076 RMVar_ID_12076 Human_SNP_ID_599122050 A-to-I Human chr16 - 28913606 28913606 28913606 GTGGTGGCGCATGCCCGTAATCCCAGCTACTCAGGAGGCTGAGGGAGGAGAATCGCTTGAACTGG GTGGTGGCGCATGCCCGTAATCCCAGCTACTCTGGAGGCTGAGGGAGGAGAATCGCTTGAACTGG T A RABEP2 Ensembl:ENSG00000177548 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs993873024 Functional Loss SNV dbSNP153 33..33 33 - - - 12077 RMVar_ID_12077 Human_SNP_ID_599122621 A-to-I Human chr16 - 28915091 28915091 28915091 GTGCCACTGCACTCCAGCCTGGGTGATAGAGCAAGACTCCATCTCAAAAAAAAAAAGGTAAAGTT GTGCCACTGCACTCCAGCCTGGGTGATAGAGCGAGACTCCATCTCAAAAAAAAAAAGGTAAAGTT T C RABEP2 Ensembl:ENSG00000177548 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs147860806 Functional Loss SNV dbSNP153 33..33 33 - - - 12078 RMVar_ID_12078 Human_SNP_ID_599122622 A-to-I Human chr16 - 28915091 28915091 28915091 GTGCCACTGCACTCCAGCCTGGGTGATAGAGCAAGACTCCATCTCAAAAAAAAAAAGGTAAAGTT GTGCCACTGCACTCCAGCCTGGGTGATAGAGCCAGACTCCATCTCAAAAAAAAAAAGGTAAAGTT T G RABEP2 Ensembl:ENSG00000177548 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs147860806 Functional Loss SNV dbSNP153 33..33 33 - - - 12079 RMVar_ID_12079 Human_SNP_ID_599122707 A-to-I Human chr16 - 28915258 28915258 28915258 GGCCTGGAGTTCAAAACCAGTCTGGGCAACATAGCAAGATCCTGTCTCCACAAAAAAATACAAAA GGCCTGGAGTTCAAAACCAGTCTGGGCAACATGGCAAGATCCTGTCTCCACAAAAAAATACAAAA T C RABEP2 Ensembl:ENSG00000177548 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs548588533 Functional Loss SNV dbSNP153 33..33 33 - - - 12080 RMVar_ID_12080 Human_SNP_ID_599122801 A-to-I Human chr16 - 28915677 28915677 28915677 AGCCGGGCGTGGTGGCGAGCGCCTGTAATCCCAGCTACTCATGAGGCTGAGGCAGGAGAATCGCT AGCCGGGCGTGGTGGCGAGCGCCTGTAATCCCGGCTACTCATGAGGCTGAGGCAGGAGAATCGCT T C RABEP2 Ensembl:ENSG00000177548 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1490875025 Functional Loss SNV dbSNP153 33..33 33 - - - 12081 RMVar_ID_12081 Human_SNP_ID_599122825 A-to-I Human chr16 - 28915744 28915744 28915744 TTTCAGGAGTTCGAGACAAGCCTGGCCAAAATAGTGAAACCCTGTCTCTACTAAAAATACAAAAA TTTCAGGAGTTCGAGACAAGCCTGGCCAAAATGGTGAAACCCTGTCTCTACTAAAAATACAAAAA T C RABEP2 Ensembl:ENSG00000177548 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1405966259 Functional Loss SNV dbSNP153 33..33 33 - - - 12082 RMVar_ID_12082 Human_SNP_ID_599122826 A-to-I Human chr16 - 28915749 28915749 28915749 GGTGGTTTCAGGAGTTCGAGACAAGCCTGGCCAAAATAGTGAAACCCTGTCTCTACTAAAAATAC GGTGGTTTCAGGAGTTCGAGACAAGCCTGGCCGAAATAGTGAAACCCTGTCTCTACTAAAAATAC T C RABEP2 Ensembl:ENSG00000177548 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs974315036 Functional Loss SNV dbSNP153 33..33 33 - - - 12083 RMVar_ID_12083 Human_SNP_ID_599122842 A-to-I Human chr16 - 28915815 28915815 28915815 AAAGTTGTCCTGGGCCAGGCACGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGT AAAGTTGTCCTGGGCCAGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGT T C RABEP2 Ensembl:ENSG00000177548 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1307415013 Functional Loss SNV dbSNP153 33..33 33 - - - 12084 RMVar_ID_12084 Human_SNP_ID_599122872 A-to-I Human chr16 - 28915925 28915925 28915925 TGAGGCAGGAGAATCGCTTGAACCTAGGAGGCAGAGGTAGCAGTGAGCAGAGATAGTGCCATTGC TGAGGCAGGAGAATCGCTTGAACCTAGGAGGCGGAGGTAGCAGTGAGCAGAGATAGTGCCATTGC T C RABEP2 Ensembl:ENSG00000177548 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1045709286 Functional Loss SNV dbSNP153 33..33 33 - - - 12085 RMVar_ID_12085 Human_SNP_ID_599122882 A-to-I Human chr16 - 28915978 28915978 28915978 AAAATTAGCTGGGCGTGGTGGCACGCATCTGTAATTCTAGCTACTTGGGAGGCTGAGGCAGGAGA AAAATTAGCTGGGCGTGGTGGCACGCATCTGTTATTCTAGCTACTTGGGAGGCTGAGGCAGGAGA T A RABEP2 Ensembl:ENSG00000177548 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1567498324 Functional Loss SNV dbSNP153 33..33 33 - - - 12086 RMVar_ID_12086 Human_SNP_ID_599122898 A-to-I Human chr16 - 28916042 28916042 28916042 GGTCTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTTAAACCCCCTTCTACTAAAAATACAAAA GGTCTCAGGAGTTCGAGACCAGCCTGGCCAACGTGGTTAAACCCCCTTCTACTAAAAATACAAAA T C RABEP2 Ensembl:ENSG00000177548 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1025908144 Functional Loss SNV dbSNP153 33..33 33 - - - 12087 RMVar_ID_12087 Human_SNP_ID_599122922 A-to-I Human chr16 - 28916137 28916137 28916137 GAAGAGTTGTCCTAGGCCAGGCACGGTGGCTCATGCCTGTAATCCTAGCACTTTGGGAGGCCGAG GAAGAGTTGTCCTAGGCCAGGCACGGTGGCTCGTGCCTGTAATCCTAGCACTTTGGGAGGCCGAG T C RABEP2 Ensembl:ENSG00000177548 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1269080089 Functional Loss SNV dbSNP153 33..33 33 - - - 12088 RMVar_ID_12088 Human_SNP_ID_599122990 A-to-I Human chr16 - 28916455 28916455 28916455 GTTGGCCAGGCTGGTTTCAAACTCCTGCCCTCAGGTGATCTGCCCGCCTTGGCCTCCCAAAGTGC GTTGGCCAGGCTGGTTTCAAACTCCTGCCCTCGGGTGATCTGCCCGCCTTGGCCTCCCAAAGTGC T C RABEP2 Ensembl:ENSG00000177548 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1420134476 Functional Loss SNV dbSNP153 33..33 33 - - - 12089 RMVar_ID_12089 Human_SNP_ID_599123118 A-to-I Human chr16 - 28916821 28916821 28916821 CACCACCACATCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCACGTTGGCCAGTC CACCACCACATCCAGCTAATTTTTGTATTTTTGGTAGAGATGGGGTTTCACCACGTTGGCCAGTC T C RABEP2 Ensembl:ENSG00000177548 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs768485094 Functional Loss SNV dbSNP153 33..33 33 - - - 12090 RMVar_ID_12090 Human_SNP_ID_599123143 A-to-I Human chr16 - 28916937 28916937 28916937 GTCCCCAGGCTGGAGTGCAGTGGTGCCATCTCAGCTCATTGCAACCTCTGCACCCAGGTCCTGGT GTCCCCAGGCTGGAGTGCAGTGGTGCCATCTCTGCTCATTGCAACCTCTGCACCCAGGTCCTGGT T A RABEP2 Ensembl:ENSG00000177548 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs181991372 Functional Loss SNV dbSNP153 33..33 33 - - - 12091 RMVar_ID_12091 Human_SNP_ID_599123295 A-to-I Human chr16 - 28917615 28917615 28917615 GAGTTTGAGACCAGCCTGGCTAACTTGGGGAAACCCCGTCTCTACTAAAAAAGTACAGAAATTAG GAGTTTGAGACCAGCCTGGCTAACTTGGGGAAGCCCCGTCTCTACTAAAAAAGTACAGAAATTAG T C RABEP2 Ensembl:ENSG00000177548 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1441355586 Functional Loss SNV dbSNP153 33..33 33 - - - 12092 RMVar_ID_12092 Human_SNP_ID_599123575 A-to-I Human chr16 - 28918493 28918493 28918493 CTCCTGCCTCAGCCTCCCGAATAGCTGGAATTACAGGCACCTGCCACCATGCCCAGCTAATTTTT CTCCTGCCTCAGCCTCCCGAATAGCTGGAATTTCAGGCACCTGCCACCATGCCCAGCTAATTTTT T A RABEP2 Ensembl:ENSG00000177548 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1374297679 Functional Loss SNV dbSNP153 33..33 33 - - - 12093 RMVar_ID_12093 Human_SNP_ID_599123580 A-to-I Human chr16 - 28918515 28918515 28918515 TGCCTCCTGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCGAATAGCTGGAATTACAGGCACCTG TGCCTCCTGGGTTCAAGTGATTCTCCTGCCTCTGCCTCCCGAATAGCTGGAATTACAGGCACCTG T A RABEP2 Ensembl:ENSG00000177548 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1442718930 Functional Loss SNV dbSNP153 33..33 33 - - - 12094 RMVar_ID_12094 Human_SNP_ID_599123585 A-to-I Human chr16 - 28918528 28918528 28918528 TCACTGCCACCTCTGCCTCCTGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCGAATAGCTGGAA TCACTGCCACCTCTGCCTCCTGGGTTCAAGTGGTTCTCCTGCCTCAGCCTCCCGAATAGCTGGAA T C RABEP2 Ensembl:ENSG00000177548 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs533337064 Functional Loss SNV dbSNP153 33..33 33 - - - 12095 RMVar_ID_12095 Human_SNP_ID_599123646 A-to-I Human chr16 - 28918790 28918790 28918790 TAAATTAACTGGGCATGGTGGTGCACACCTGTAGTCCCAGCTACTCAAGAGGCTGACATGGGAGG TAAATTAACTGGGCATGGTGGTGCACACCTGTGGTCCCAGCTACTCAAGAGGCTGACATGGGAGG T C RABEP2 Ensembl:ENSG00000177548 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs893020461 Functional Loss SNV dbSNP153 33..33 33 - - - 12096 RMVar_ID_12096 Human_SNP_ID_599124084 A-to-I Human chr16 - 28920488 28920488 28920488 CCAGCTACACAGGACGCTGAGGCACGAGAATCACTTGAACCCAGCAGGCAGAGGTTGCAGTGAGC CCAGCTACACAGGACGCTGAGGCACGAGAATCGCTTGAACCCAGCAGGCAGAGGTTGCAGTGAGC T C RABEP2 Ensembl:ENSG00000177548 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1433721788 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67124 12097 RMVar_ID_12097 Human_SNP_ID_599133090 A-to-I Human chr16 + 28953214 28953214 28953214 CTCCTGCCTCAGCCTCCCGAGTAGCAGGGATTACAGGCGCCCGCCACCATGTCTGGCTTTTTTGT CTCCTGCCTCAGCCTCCCGAGTAGCAGGGATTGCAGGCGCCCGCCACCATGTCTGGCTTTTTTGT A G NFATC2IP Ensembl:ENSG00000176953 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1567512210 Functional Loss SNV dbSNP153 33..33 33 - - - 12098 RMVar_ID_12098 Human_SNP_ID_599133228 A-to-I Human chr16 + 28953843 28953843 28953843 AGGAGGCTGAGGTGGGAGAAACACCTGAGCCCAGGAAGTCGAGGCTGCAGTGAGCCATGATCATG AGGAGGCTGAGGTGGGAGAAACACCTGAGCCCGGGAAGTCGAGGCTGCAGTGAGCCATGATCATG A G NFATC2IP Ensembl:ENSG00000176953 Protein coding intron GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs1351272471 Functional Loss SNV dbSNP153 33..33 33 - - - 12099 RMVar_ID_12099 Human_SNP_ID_599133581 A-to-I Human chr16 + 28955104 28955104 28955104 TGATCCCAGCTGCTCGGGAGGCTGAGATGGGAAAATCGCTTGATCCCAGGAGTTAGAGGCTGCAG TGATCCCAGCTGCTCGGGAGGCTGAGATGGGACAATCGCTTGATCCCAGGAGTTAGAGGCTGCAG A C NFATC2IP Ensembl:ENSG00000176953 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1347390864 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_177693,RMVar_hsa_circ_336064 12100 RMVar_ID_12100 Human_SNP_ID_599133593 A-to-I Human chr16 + 28955157 28955157 28955157 TAGAGGCTGCAGTGAGCCATGATCGTGCCACTATACTCCAGCCTGGGTGACAGAGTGAGACCCTG TAGAGGCTGCAGTGAGCCATGATCGTGCCACTGTACTCCAGCCTGGGTGACAGAGTGAGACCCTG A G NFATC2IP Ensembl:ENSG00000176953 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1421416161 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12713105,Human_RBP_ID_25243678 RMVar_hsa_circ_177693,RMVar_hsa_circ_336064 12101 RMVar_ID_12101 Human_SNP_ID_599133637 A-to-I Human chr16 + 28955305 28955305 28955305 AGTCAATCAAGAGTTAACACTTGGCTAGGCACAATGGCTCTTGCCTGTAATCCCAGCACTTTGGG AGTCAATCAAGAGTTAACACTTGGCTAGGCACGATGGCTCTTGCCTGTAATCCCAGCACTTTGGG A G NFATC2IP Ensembl:ENSG00000176953 Protein coding intron GSE38233;GSE100210;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,29129909,29796672,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs951418320 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17565004 RMVar_hsa_circ_177693,RMVar_hsa_circ_336064 12102 RMVar_ID_12102 Human_SNP_ID_599133638 A-to-I Human chr16 + 28955305 28955305 28955305 AGTCAATCAAGAGTTAACACTTGGCTAGGCACAATGGCTCTTGCCTGTAATCCCAGCACTTTGGG AGTCAATCAAGAGTTAACACTTGGCTAGGCACTATGGCTCTTGCCTGTAATCCCAGCACTTTGGG A T NFATC2IP Ensembl:ENSG00000176953 Protein coding intron GSE38233;GSE100210;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,29129909,29796672,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs951418320 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17565004 RMVar_hsa_circ_177693,RMVar_hsa_circ_336064 12103 RMVar_ID_12103 Human_SNP_ID_599133706 A-to-I Human chr16 + 28955630 28955630 28955630 ATGTATTTTTACATTTTTAGAGATAGGGCCTCACTCCATTGCCCAGGCTGGAGTGCAGTGGCGTG ATGTATTTTTACATTTTTAGAGATAGGGCCTCCCTCCATTGCCCAGGCTGGAGTGCAGTGGCGTG A C NFATC2IP Ensembl:ENSG00000176953 Protein coding intron GSE100210;GSE99789 HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 29129909,29796672 RNA-Seq:(High) rs1309689718 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12713115,Human_RBP_ID_17564091,Human_RBP_ID_25203984 RMVar_hsa_circ_177693,RMVar_hsa_circ_336064 12104 RMVar_ID_12104 Human_SNP_ID_599133708 A-to-I Human chr16 + 28955635 28955635 28955635 TTTTTACATTTTTAGAGATAGGGCCTCACTCCATTGCCCAGGCTGGAGTGCAGTGGCGTGATCAT TTTTTACATTTTTAGAGATAGGGCCTCACTCCGTTGCCCAGGCTGGAGTGCAGTGGCGTGATCAT A G NFATC2IP Ensembl:ENSG00000176953 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1567512869 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12713117,Human_RBP_ID_17564091,Human_RBP_ID_20111703,Human_RBP_ID_25203984 RMVar_hsa_circ_177693,RMVar_hsa_circ_336064 12105 RMVar_ID_12105 Human_SNP_ID_599133731 A-to-I Human chr16 + 28955740 28955740 28955740 CCCACCTCAGCCTCCTGAGTAGCTGGGACTACAGCTGTGTTCTACTATGCCTGGCTAATTATGTA CCCACCTCAGCCTCCTGAGTAGCTGGGACTACGGCTGTGTTCTACTATGCCTGGCTAATTATGTA A G NFATC2IP Ensembl:ENSG00000176953 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs557651774 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17564093 RMVar_hsa_circ_177693,RMVar_hsa_circ_336064 12106 RMVar_ID_12106 Human_SNP_ID_599133744 A-to-I Human chr16 + 28955798 28955798 28955798 TTATGTAGAAATAGGGTCTCCCCATCTTGCCCAGCCTGGTCTTGGACTCCTGGGCTCGAGCGATC TTATGTAGAAATAGGGTCTCCCCATCTTGCCCTGCCTGGTCTTGGACTCCTGGGCTCGAGCGATC A T NFATC2IP Ensembl:ENSG00000176953 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs899863757 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17564093 RMVar_hsa_circ_177693,RMVar_hsa_circ_336064 12107 RMVar_ID_12107 Human_SNP_ID_599134093 A-to-I Human chr16 + 28957065 28957065 28957065 TTTATTATTTTTATTTTTTGAGACGGGGTCTCACTCTGTCGCCTAGGCTGGAGTGCAGTGGCACG TTTATTATTTTTATTTTTTGAGACGGGGTCTCGCTCTGTCGCCTAGGCTGGAGTGCAGTGGCACG A G NFATC2IP Ensembl:ENSG00000176953 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs957221273 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5128572 RMVar_hsa_circ_78324,RMVar_hsa_circ_177693,RMVar_hsa_circ_336064,RMVar_hsa_circ_285448,RMVar_hsa_circ_177694,RMVar_hsa_circ_177695 12108 RMVar_ID_12108 Human_SNP_ID_599134101 A-to-I Human chr16 + 28957095 28957095 28957095 TCACTCTGTCGCCTAGGCTGGAGTGCAGTGGCACGATCTCTGCTCACTGAAACCTCCGCCTCCCA TCACTCTGTCGCCTAGGCTGGAGTGCAGTGGCGCGATCTCTGCTCACTGAAACCTCCGCCTCCCA A G NFATC2IP Ensembl:ENSG00000176953 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs924588912 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78324,RMVar_hsa_circ_177693,RMVar_hsa_circ_336064,RMVar_hsa_circ_285448,RMVar_hsa_circ_177694,RMVar_hsa_circ_177695 12109 RMVar_ID_12109 Human_SNP_ID_599134128 A-to-I Human chr16 + 28957214 28957214 28957214 CGCCACCATGCCCGACTAATTTATGTATTTTTAGTGGAGGCAGGGCTTCACCATATTGGCCAGGC CGCCACCATGCCCGACTAATTTATGTATTTTTGGTGGAGGCAGGGCTTCACCATATTGGCCAGGC A G NFATC2IP Ensembl:ENSG00000176953 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1416281873 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78324,RMVar_hsa_circ_177693,RMVar_hsa_circ_336064,RMVar_hsa_circ_285448,RMVar_hsa_circ_177694,RMVar_hsa_circ_177695 12110 RMVar_ID_12110 Human_SNP_ID_599134132 A-to-I Human chr16 + 28957234 28957234 28957234 TTATGTATTTTTAGTGGAGGCAGGGCTTCACCATATTGGCCAGGCTGGTCTTGAACTCCTGATCT TTATGTATTTTTAGTGGAGGCAGGGCTTCACCGTATTGGCCAGGCTGGTCTTGAACTCCTGATCT A G NFATC2IP Ensembl:ENSG00000176953 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs577915519 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20111750 RMVar_hsa_circ_78324,RMVar_hsa_circ_177693,RMVar_hsa_circ_336064,RMVar_hsa_circ_285448,RMVar_hsa_circ_177694,RMVar_hsa_circ_177695 12111 RMVar_ID_12111 Human_SNP_ID_599134189 A-to-I Human chr16 + 28957482 28957482 28957482 CTGGGCAAAATAGTGAGACCTTGTCTCTACTAAAAATAAAAAAATTAACCAGGCATGGTGGCACA CTGGGCAAAATAGTGAGACCTTGTCTCTACTACAAATAAAAAAATTAACCAGGCATGGTGGCACA A C NFATC2IP Ensembl:ENSG00000176953 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1192552990 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78324,RMVar_hsa_circ_177693,RMVar_hsa_circ_336064,RMVar_hsa_circ_285448,RMVar_hsa_circ_177694,RMVar_hsa_circ_177695 12112 RMVar_ID_12112 Human_SNP_ID_599134203 A-to-I Human chr16 + 28957568 28957568 28957568 GGGAGGCTGATGCAAGAGGATCTTCTGAGTCCAGGAGTTGGGGGCTGCAGTCAGCTGTGATCATG GGGAGGCTGATGCAAGAGGATCTTCTGAGTCCGGGAGTTGGGGGCTGCAGTCAGCTGTGATCATG A G NFATC2IP Ensembl:ENSG00000176953 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs995874969 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5128573,Human_RBP_ID_6506460,Human_RBP_ID_12713185,Human_RBP_ID_17563737,Human_RBP_ID_22473809 RMVar_hsa_circ_78324,RMVar_hsa_circ_177693,RMVar_hsa_circ_336064,RMVar_hsa_circ_285448,RMVar_hsa_circ_177694,RMVar_hsa_circ_177695 12113 RMVar_ID_12113 Human_SNP_ID_599134208 A-to-I Human chr16 + 28957598 28957598 28957598 CCAGGAGTTGGGGGCTGCAGTCAGCTGTGATCATGCCACTGCACTGCAGCCTGGGTGAGAGAGCA CCAGGAGTTGGGGGCTGCAGTCAGCTGTGATCCTGCCACTGCACTGCAGCCTGGGTGAGAGAGCA A C NFATC2IP Ensembl:ENSG00000176953 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs565587061 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5128573,Human_RBP_ID_9824450,Human_RBP_ID_17563737,Human_RBP_ID_22473809,Human_RBP_ID_22945690,Human_RBP_ID_23163747,Human_RBP_ID_25204029 RMVar_hsa_circ_78324,RMVar_hsa_circ_177693,RMVar_hsa_circ_336064,RMVar_hsa_circ_285448,RMVar_hsa_circ_177694,RMVar_hsa_circ_177695 12114 RMVar_ID_12114 Human_SNP_ID_599134209 A-to-I Human chr16 + 28957598 28957598 28957598 CCAGGAGTTGGGGGCTGCAGTCAGCTGTGATCATGCCACTGCACTGCAGCCTGGGTGAGAGAGCA CCAGGAGTTGGGGGCTGCAGTCAGCTGTGATCGTGCCACTGCACTGCAGCCTGGGTGAGAGAGCA A G NFATC2IP Ensembl:ENSG00000176953 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs565587061 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5128573,Human_RBP_ID_9824450,Human_RBP_ID_17563737,Human_RBP_ID_22473809,Human_RBP_ID_22945690,Human_RBP_ID_23163747,Human_RBP_ID_25204029 RMVar_hsa_circ_78324,RMVar_hsa_circ_177693,RMVar_hsa_circ_336064,RMVar_hsa_circ_285448,RMVar_hsa_circ_177694,RMVar_hsa_circ_177695 12115 RMVar_ID_12115 Human_SNP_ID_599134269 A-to-I Human chr16 + 28957899 28957899 28957899 CACGCCTGTAATCCCAGCACTTTTGGGAGGTGAAGGCAGGCAGATCACCTGAGGTCAGGAGTTCG CACGCCTGTAATCCCAGCACTTTTGGGAGGTGGAGGCAGGCAGATCACCTGAGGTCAGGAGTTCG A G NFATC2IP Ensembl:ENSG00000176953 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs908022409 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17564096 RMVar_hsa_circ_78324,RMVar_hsa_circ_177693,RMVar_hsa_circ_336064,RMVar_hsa_circ_285448,RMVar_hsa_circ_177694,RMVar_hsa_circ_177695 12116 RMVar_ID_12116 Human_SNP_ID_599134798 A-to-I Human chr16 + 28959652 28959652 28959652 GGCTGAAGTCTGGCATGATCTTGGCTCACTGCAGCCTCTGCCTTCCGAGTTTCAAGTGATTCTCT GGCTGAAGTCTGGCATGATCTTGGCTCACTGCGGCCTCTGCCTTCCGAGTTTCAAGTGATTCTCT A G NFATC2IP Ensembl:ENSG00000176953 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs370937985 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91884,RMVar_hsa_circ_177698 12117 RMVar_ID_12117 Human_SNP_ID_599134825 A-to-I Human chr16 + 28959748 28959748 28959748 GGTGCACGTGCTGGGCTAATTTTTGCATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGC GGTGCACGTGCTGGGCTAATTTTTGCATTTTTCGTAGAGACAGGGTTTCACCATGTTGGCCAGGC A C NFATC2IP Ensembl:ENSG00000176953 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs980655667 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91884,RMVar_hsa_circ_177698 12118 RMVar_ID_12118 Human_SNP_ID_599135166 A-to-I Human chr16 + 28961146 28961146 28961146 GCTCAGGAGTTCAAGACCAGCCCGGGCAACATAGTGAAACCCTGCCTCTACAAAAAATACAAAAA GCTCAGGAGTTCAAGACCAGCCCGGGCAACATGGTGAAACCCTGCCTCTACAAAAAATACAAAAA A G NFATC2IP Ensembl:ENSG00000176953 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1322354323 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91884,RMVar_hsa_circ_177698 12119 RMVar_ID_12119 Human_SNP_ID_599135441 A-to-I Human chr16 + 28962045 28962045 28962045 TCTACCTCAGCCTCCTGAGTAGTTGGGACTACAGGTGTGTGCCACTACCCTTGGCTAATTTTTTA TCTACCTCAGCCTCCTGAGTAGTTGGGACTACGGGTGTGTGCCACTACCCTTGGCTAATTTTTTA A G NFATC2IP Ensembl:ENSG00000176953 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1053508997 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91884,RMVar_hsa_circ_177698 12120 RMVar_ID_12120 Human_SNP_ID_599135673 A-to-I Human chr16 + 28963107 28963107 28963107 AGGAGGCTGAGGCAGGAGAATTGCTTGAACCCAGGAGGCAGAGGTTGCAGTGAGTTGTCTACCAG AGGAGGCTGAGGCAGGAGAATTGCTTGAACCCGGGAGGCAGAGGTTGCAGTGAGTTGTCTACCAG A G NFATC2IP Ensembl:ENSG00000176953 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs978221975 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91884,RMVar_hsa_circ_177698 12121 RMVar_ID_12121 Human_SNP_ID_599140140 A-to-I Human chr16 + 28980331 28980331 28980331 ATTTTTTTTTTTTGTAGAGATGGGGTCTTTGTATGTTGCCCAGGTTGGTTTTGAACTCCTGGCCT ATTTTTTTTTTTTGTAGAGATGGGGTCTTTGTGTGTTGCCCAGGTTGGTTTTGAACTCCTGGCCT A G SPNS1,AC109460.3 Ensembl:ENSG00000169682,Ensembl:ENSG00000261067 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569845904 Functional Loss SNV dbSNP153 33..33 33 - - - 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 12122 RMVar_ID_12122 Human_SNP_ID_599175925 A-to-I Human chr16 + 29119669 29119669 29119669 ACCCCCATCTCTACAAAAAAATTTAAAAAATTAGCTGGGCACAGTAGAACCTGCCTATAATCCCT ACCCCCATCTCTACAAAAAAATTTAAAAAATTGGCTGGGCACAGTAGAACCTGCCTATAATCCCT A G AC009093.8 Ensembl:ENSG00000284649 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1439611568 Functional Loss SNV dbSNP153 33..33 33 - - - 12123 RMVar_ID_12123 Human_SNP_ID_599252041 A-to-I Human chr16 - 29407005 29407005 29407005 AGATCCCACCACTGCACTCCAGCTTAGGCAACAGAGCCAGACTGTGTCTCAAAAACAGGAAAGAA AGATCCCACCACTGCACTCCAGCTTAGGCAACGGAGCCAGACTGTGTCTCAAAAACAGGAAAGAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1391412773 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12713825 12124 RMVar_ID_12124 Human_SNP_ID_599252128 A-to-I Human chr16 - 29407242 29407242 29407242 AAATTAGGCTGGGCACGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGCAGAG AAATTAGGCTGGGCACGGTGGCTCACACCTGTCATCCCAGCACTTTGGGAGGCCGAGGCGCAGAG T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1233106642 Functional Loss SNV dbSNP153 33..33 33 - - - 12125 RMVar_ID_12125 Human_SNP_ID_599253461 A-to-I Human chr16 - 29410980 29410980 29410980 ATTAACATTAAAACAGAGATCTTAAGCTGGGCACAGTGGCTCATGCCTGTAATCCCAGCACTTTG ATTAACATTAAAACAGAGATCTTAAGCTGGGCGCAGTGGCTCATGCCTGTAATCCCAGCACTTTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904703134 Functional Loss SNV dbSNP153 33..33 33 - - - 12126 RMVar_ID_12126 Human_SNP_ID_599257749 A-to-I Human chr16 - 29424240 29424240 29424240 GTGTGGGCCGGGCACGGTGGCTAACGCCTGTAATCCCAGCACTTTGAGATGCTGAGGCGGGTGGA GTGTGGGCCGGGCACGGTGGCTAACGCCTGTAGTCCCAGCACTTTGAGATGCTGAGGCGGGTGGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1281381904 Functional Loss SNV dbSNP153 33..33 33 - - - 12127 RMVar_ID_12127 Human_SNP_ID_599280693 A-to-I Human chr16 - 29587529 29587529 29587529 AGATCATGCCATTGCACTCCAATTTGGGTGACAGAGCGAGACTGTCTCAAAAACAAAAACAAAAA AGATCATGCCATTGCACTCCAATTTGGGTGACTGAGCGAGACTGTCTCAAAAACAAAAACAAAAA T A SMG1P2 Ensembl:ENSG00000205534 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1208819829 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17206497,Human_RBP_ID_17373391,Human_RBP_ID_17564098,Human_RBP_ID_18513229,Human_RBP_ID_18530073 RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 12128 RMVar_ID_12128 Human_SNP_ID_599280857 A-to-I Human chr16 - 29588169 29588169 29588169 TCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCATGTGCCACTACTCCTG TCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTGGCTGGGATTACAGGCATGTGCCACTACTCCTG T C SMG1P2 Ensembl:ENSG00000205534 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1184586556 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 12129 RMVar_ID_12129 Human_SNP_ID_599281141 A-to-I Human chr16 - 29588901 29588901 29588901 CACGTGCCTCTGCCTCCCGAGTAGCTGGGACTACAGGTGCATGTCACCAGGCCTGGCTAATTTTT CACGTGCCTCTGCCTCCCGAGTAGCTGGGACTGCAGGTGCATGTCACCAGGCCTGGCTAATTTTT T C SMG1P2 Ensembl:ENSG00000205534 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1233096722 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12714195 RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 12130 RMVar_ID_12130 Human_SNP_ID_599301120 A-to-I Human chr16 + 29665124 29665124 29665124 GTCGCCCAGGCTGGAGTGCAATGCACGATCTCAGTTCACTGCAACCTCTGCCTCCTAAGTTCAGG GTCGCCCAGGCTGGAGTGCAATGCACGATCTCGGTTCACTGCAACCTCTGCCTCCTAAGTTCAGG A G SPN,QPRT Ensembl:ENSG00000197471,Ensembl:ENSG00000103485 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1036483145 Functional Loss SNV dbSNP153 33..33 33 - - - 12131 RMVar_ID_12131 Human_SNP_ID_599301975 A-to-I Human chr16 + 29667595 29667595 29667595 GTCAGGAGTTTGAGACCAGCCTGGCCAATATGATGAAACCCCGTTTCTACTAAAAATACAAAAGT GTCAGGAGTTTGAGACCAGCCTGGCCAATATGTTGAAACCCCGTTTCTACTAAAAATACAAAAGT A T SPN,QPRT Ensembl:ENSG00000197471,Ensembl:ENSG00000103485 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs925408519 Functional Loss SNV dbSNP153 33..33 33 - - - 12132 RMVar_ID_12132 Human_SNP_ID_599301979 A-to-I Human chr16 + 29667620 29667620 29667620 CAATATGATGAAACCCCGTTTCTACTAAAAATACAAAAGTTAGCCAGGCATGGTGGTGTGCTCCT CAATATGATGAAACCCCGTTTCTACTAAAAATGCAAAAGTTAGCCAGGCATGGTGGTGTGCTCCT A G SPN,QPRT Ensembl:ENSG00000197471,Ensembl:ENSG00000103485 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1258960241 Functional Loss SNV dbSNP153 33..33 33 - - - 12133 RMVar_ID_12133 Human_SNP_ID_599301985 A-to-I Human chr16 + 29667655 29667655 29667655 AAAGTTAGCCAGGCATGGTGGTGTGCTCCTGTAATCCCAGCTACTTAGGAGGCTGAGGCCAGAGA AAAGTTAGCCAGGCATGGTGGTGTGCTCCTGTGATCCCAGCTACTTAGGAGGCTGAGGCCAGAGA A G SPN,QPRT Ensembl:ENSG00000197471,Ensembl:ENSG00000103485 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs935599080 Functional Loss SNV dbSNP153 33..33 33 - - - 12134 RMVar_ID_12134 Human_SNP_ID_599301988 A-to-I Human chr16 + 29667669 29667669 29667669 ATGGTGGTGTGCTCCTGTAATCCCAGCTACTTAGGAGGCTGAGGCCAGAGAATTGCTTGAACCCT ATGGTGGTGTGCTCCTGTAATCCCAGCTACTTTGGAGGCTGAGGCCAGAGAATTGCTTGAACCCT A T SPN,QPRT Ensembl:ENSG00000197471,Ensembl:ENSG00000103485 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs543302261 Functional Loss SNV dbSNP153 33..33 33 - - - 12135 RMVar_ID_12135 Human_SNP_ID_599302164 A-to-I Human chr16 + 29668229 29668229 29668229 TATGAGAACCACCACACCTGGCTAATTTTTGTATTTTTTGTAGAGATGGGGTTTCACCATGTTGT TATGAGAACCACCACACCTGGCTAATTTTTGTGTTTTTTGTAGAGATGGGGTTTCACCATGTTGT A G SPN,QPRT Ensembl:ENSG00000197471,Ensembl:ENSG00000103485 Protein coding,Protein coding 3'UTR,intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs754277824 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_129294,Human_RBP_ID_17563753 12136 RMVar_ID_12136 Human_SNP_ID_599302195 A-to-I Human chr16 + 29668335 29668335 29668335 CCTCAGCCTCCCAAAATGCTGGGACTATAGGCATGAGCCACTGCACCCAGCCACTGCTTCATTCC CCTCAGCCTCCCAAAATGCTGGGACTATAGGCTTGAGCCACTGCACCCAGCCACTGCTTCATTCC A T SPN,QPRT Ensembl:ENSG00000197471,Ensembl:ENSG00000103485 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1458536368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17564641 12137 RMVar_ID_12137 Human_SNP_ID_599302339 A-to-I Human chr16 + 29668892 29668892 29668892 GGAGCAGATCCAGCGCAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCAGAGCAGGGAGG GGAGCAGATCCAGCGCAGTGGCTCATGCCTGTTATCCCAGCACTTTGGGAGGCAGAGCAGGGAGG A T SPN,QPRT Ensembl:ENSG00000197471,Ensembl:ENSG00000103485 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1450177768 Functional Loss SNV dbSNP153 33..33 33 - - - 12138 RMVar_ID_12138 Human_SNP_ID_599302379 A-to-I Human chr16 + 29669068 29669068 29669068 TACTTGAGAAGCTGAGGCAGGAGGACTGCTTGAAGCCAGGAGTTTGAGACCAGCCTGGGCAACAT TACTTGAGAAGCTGAGGCAGGAGGACTGCTTGCAGCCAGGAGTTTGAGACCAGCCTGGGCAACAT A C SPN,QPRT Ensembl:ENSG00000197471,Ensembl:ENSG00000103485 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs12929333 Functional Loss SNV dbSNP153 33..33 33 - - - 12139 RMVar_ID_12139 Human_SNP_ID_599302466 A-to-I Human chr16 + 29669375 29669375 29669375 AGGCATGCACCACCAAACCCGGATAATTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGG AGGCATGCACCACCAAACCCGGATAATTTTGTGTTTTTAGTAGAGATGGGGTTTCACCATGTTGG A G SPN,QPRT Ensembl:ENSG00000197471,Ensembl:ENSG00000103485 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1401151246 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_128035 12140 RMVar_ID_12140 Human_SNP_ID_599302468 A-to-I Human chr16 + 29669381 29669381 29669381 GCACCACCAAACCCGGATAATTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGTCAAGC GCACCACCAAACCCGGATAATTTTGTATTTTTGGTAGAGATGGGGTTTCACCATGTTGGTCAAGC A G SPN,QPRT Ensembl:ENSG00000197471,Ensembl:ENSG00000103485 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs530018878 Functional Loss SNV dbSNP153 33..33 33 - - - 12141 RMVar_ID_12141 Human_SNP_ID_599302474 A-to-I Human chr16 + 29669410 29669410 29669410 TTTAGTAGAGATGGGGTTTCACCATGTTGGTCAAGCTGGTCTTGAACTCCCGACCTCTGCTGATC TTTAGTAGAGATGGGGTTTCACCATGTTGGTCCAGCTGGTCTTGAACTCCCGACCTCTGCTGATC A C SPN,QPRT Ensembl:ENSG00000197471,Ensembl:ENSG00000103485 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1246056207 Functional Loss SNV dbSNP153 33..33 33 - - - 12142 RMVar_ID_12142 Human_SNP_ID_599302490 A-to-I Human chr16 + 29669475 29669475 29669475 CGTATGCCTCGGCCTCCCAAAGTGCTGGGATTACATGCGTGAGCCACCGTGCCCGACAATAGATG CGTATGCCTCGGCCTCCCAAAGTGCTGGGATTGCATGCGTGAGCCACCGTGCCCGACAATAGATG A G SPN,QPRT Ensembl:ENSG00000197471,Ensembl:ENSG00000103485 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1451594823 Functional Loss SNV dbSNP153 33..33 33 - - - 12143 RMVar_ID_12143 Human_SNP_ID_599302539 A-to-I Human chr16 + 29669670 29669670 29669670 GGGAGGCCGAGGCAGGTGGATCACCTGAGGTCAGGAGTTCAAGACCAGCCTGACCAACATGGTGA GGGAGGCCGAGGCAGGTGGATCACCTGAGGTCGGGAGTTCAAGACCAGCCTGACCAACATGGTGA A G SPN,QPRT Ensembl:ENSG00000197471,Ensembl:ENSG00000103485 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1397354022 Functional Loss SNV dbSNP153 33..33 33 - - - 12144 RMVar_ID_12144 Human_SNP_ID_599302545 A-to-I Human chr16 + 29669678 29669678 29669678 GAGGCAGGTGGATCACCTGAGGTCAGGAGTTCAAGACCAGCCTGACCAACATGGTGAAACCCTGT GAGGCAGGTGGATCACCTGAGGTCAGGAGTTCGAGACCAGCCTGACCAACATGGTGAAACCCTGT A G SPN,QPRT Ensembl:ENSG00000197471,Ensembl:ENSG00000103485 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1445260706 Functional Loss SNV dbSNP153 33..33 33 - - - 12145 RMVar_ID_12145 Human_SNP_ID_599302549 A-to-I Human chr16 + 29669690 29669690 29669690 TCACCTGAGGTCAGGAGTTCAAGACCAGCCTGACCAACATGGTGAAACCCTGTTTCAAAATACAA TCACCTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCCTGTTTCAAAATACAA A G SPN,QPRT Ensembl:ENSG00000197471,Ensembl:ENSG00000103485 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1285454509 Functional Loss SNV dbSNP153 33..33 33 - - - 12146 RMVar_ID_12146 Human_SNP_ID_599302576 A-to-I Human chr16 + 29669761 29669761 29669761 AGCTGGGCGTGGTGGCGGGCACCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCCCT AGCTGGGCGTGGTGGCGGGCACCTGTAATCCCGGCTACTTGGGAGGCTGAGGCAGGAGAATCCCT A G SPN,QPRT Ensembl:ENSG00000197471,Ensembl:ENSG00000103485 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs574648036 Functional Loss SNV dbSNP153 33..33 33 - - - 12147 RMVar_ID_12147 Human_SNP_ID_599302622 A-to-I Human chr16 + 29669950 29669950 29669950 AGTTGGGTGCAGTGGCTATGCGGTGGCACTATAGGAGGCTGAGGCGGGCAGATCACCTGAGGTCA AGTTGGGTGCAGTGGCTATGCGGTGGCACTATGGGAGGCTGAGGCGGGCAGATCACCTGAGGTCA A G SPN,QPRT Ensembl:ENSG00000197471,Ensembl:ENSG00000103485 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs190537510 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17563762,Human_RBP_ID_26445988 12148 RMVar_ID_12148 Human_SNP_ID_599302633 A-to-I Human chr16 + 29669982 29669982 29669982 AGGAGGCTGAGGCGGGCAGATCACCTGAGGTCAGGAGTTGGAGACCAGCCTGGGCAACATAGACC AGGAGGCTGAGGCGGGCAGATCACCTGAGGTCTGGAGTTGGAGACCAGCCTGGGCAACATAGACC A T SPN,QPRT Ensembl:ENSG00000197471,Ensembl:ENSG00000103485 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1272203441 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17563763,Human_RBP_ID_26445988 12149 RMVar_ID_12149 Human_SNP_ID_599302642 A-to-I Human chr16 + 29670018 29670018 29670018 GTTGGAGACCAGCCTGGGCAACATAGACCCCTATCTCTACAAAAAATTTGAAATATGAAAAATTA GTTGGAGACCAGCCTGGGCAACATAGACCCCTGTCTCTACAAAAAATTTGAAATATGAAAAATTA A G SPN,QPRT Ensembl:ENSG00000197471,Ensembl:ENSG00000103485 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs758704658 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17563763,Human_RBP_ID_26445988 12150 RMVar_ID_12150 Human_SNP_ID_599302650 A-to-I Human chr16 + 29670050 29670050 29670050 ATCTCTACAAAAAATTTGAAATATGAAAAATTAGCCAGGTGTAGTGGTGTGCGCCTGTGGTACCA ATCTCTACAAAAAATTTGAAATATGAAAAATTCGCCAGGTGTAGTGGTGTGCGCCTGTGGTACCA A C SPN,QPRT Ensembl:ENSG00000197471,Ensembl:ENSG00000103485 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1357456649 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17563764,Human_RBP_ID_26445015 12151 RMVar_ID_12151 Human_SNP_ID_599302737 A-to-I Human chr16 + 29670421 29670421 29670421 TGAGGCAGAAGAATTGCTTGAAACCGGGAGGCAGAGGTTGCAGTGAGCCGAGATCGTGTCATTGC TGAGGCAGAAGAATTGCTTGAAACCGGGAGGCGGAGGTTGCAGTGAGCCGAGATCGTGTCATTGC A G SPN,QPRT Ensembl:ENSG00000197471,Ensembl:ENSG00000103485 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs779771534 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17564654 12152 RMVar_ID_12152 Human_SNP_ID_599302892 A-to-I Human chr16 + 29671038 29671038 29671038 AGGTTTGTTTTTGTTTTTGTTTTTGTTTTTTGAGACGGAGTCTCACCCTGTCACCCAGGCTGGAG AGGTTTGTTTTTGTTTTTGTTTTTGTTTTTTGGGACGGAGTCTCACCCTGTCACCCAGGCTGGAG A G QPRT Ensembl:ENSG00000103485 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1340436169 Functional Loss SNV dbSNP153 33..33 33 - - - 12153 RMVar_ID_12153 Human_SNP_ID_599303626 A-to-I Human chr16 + 29673651 29673651 29673651 AAACAACACAGGTCGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAAGCTGAGGTGAGAGG AAACAACACAGGTCGCAGTGGCTCACACCTGTTATCCCAGCACTTTGGGAAGCTGAGGTGAGAGG A T QPRT Ensembl:ENSG00000103485 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1166955133 Functional Loss SNV dbSNP153 33..33 33 - - - 12154 RMVar_ID_12154 Human_SNP_ID_599303663 A-to-I Human chr16 + 29673796 29673796 29673796 GGGCCTGGTGATGCACACCTGTAGTCCCAGCTACTTGGGAGGCTGAGGTGGGAGGACAGCTTGAA GGGCCTGGTGATGCACACCTGTAGTCCCAGCTGCTTGGGAGGCTGAGGTGGGAGGACAGCTTGAA A G QPRT Ensembl:ENSG00000103485 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1485775564 Functional Loss SNV dbSNP153 33..33 33 - - - 12155 RMVar_ID_12155 Human_SNP_ID_599303979 A-to-I Human chr16 + 29674956 29674956 29674956 CCTTGGTCTTCCAAAGTGCTGGGATTACAGGTATGAGCCACCGCGCCTGGCCTTATTTGTTTATT CCTTGGTCTTCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCGCCTGGCCTTATTTGTTTATT A G QPRT Ensembl:ENSG00000103485 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs375155666 Functional Loss SNV dbSNP153 33..33 33 - - - 12156 RMVar_ID_12156 Human_SNP_ID_599306232 A-to-I Human chr16 + 29683425 29683425 29683425 TTGCCTAGGCCAGAGTGCAGTAGCTCCATCATAGCTCACTGCAGCCTCCAACTCCTGGACTCAAG TTGCCTAGGCCAGAGTGCAGTAGCTCCATCATGGCTCACTGCAGCCTCCAACTCCTGGACTCAAG A G QPRT Ensembl:ENSG00000103485 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1214439758 Functional Loss SNV dbSNP153 33..33 33 - - - 12157 RMVar_ID_12157 Human_SNP_ID_599309665 A-to-I Human chr16 + 29695834 29695834 29695834 TTTTTTTTTTTTTTTTGAGATGGGGTCTCACTATGTTGCCCAGGCTGGTCTCAAACTTCTGGACT TTTTTTTTTTTTTTTTGAGATGGGGTCTCACTGTGTTGCCCAGGCTGGTCTCAAACTTCTGGACT A G QPRT Ensembl:ENSG00000103485 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1409999710 Functional Loss SNV dbSNP153 33..33 33 - - - 12158 RMVar_ID_12158 Human_SNP_ID_599309747 A-to-I Human chr16 + 29696308 29696308 29696308 GTCCAGGAGTCTGAGACCAGCCTGGGCCATATAGCAAGATTCTGTCTCTACAAAAAATTAAAAAA GTCCAGGAGTCTGAGACCAGCCTGGGCCATATCGCAAGATTCTGTCTCTACAAAAAATTAAAAAA A C QPRT Ensembl:ENSG00000103485 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037860924 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12714538 12159 RMVar_ID_12159 Human_SNP_ID_599309768 A-to-I Human chr16 + 29696405 29696405 29696405 CCAGCCACTTGGGAGGCTGAGGTGGGAGGATCACTTGATCCCAGGAGGTGGAGGCTGCAGTGAAC CCAGCCACTTGGGAGGCTGAGGTGGGAGGATCGCTTGATCCCAGGAGGTGGAGGCTGCAGTGAAC A G QPRT Ensembl:ENSG00000103485 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs954300616 Functional Loss SNV dbSNP153 33..33 33 - - - 12160 RMVar_ID_12160 Human_SNP_ID_599309805 A-to-I Human chr16 + 29696527 29696527 29696527 AACAGTGGCCAGGTGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGATGGGTGG AACAGTGGCCAGGTGCGGTGGCTCACGCCTGTTATCCCAGCACTTTGGGAGGCTGAGATGGGTGG A T QPRT Ensembl:ENSG00000103485 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1434929124 Functional Loss SNV dbSNP153 33..33 33 - - - 12161 RMVar_ID_12161 Human_SNP_ID_599309817 A-to-I Human chr16 + 29696574 29696574 29696574 GGAGGCTGAGATGGGTGGATCACGAGGTCATGAGTTAGAGACCATCCTGGCCACCATGGTGAAAC GGAGGCTGAGATGGGTGGATCACGAGGTCATGCGTTAGAGACCATCCTGGCCACCATGGTGAAAC A C QPRT Ensembl:ENSG00000103485 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs990483031 Functional Loss SNV dbSNP153 33..33 33 - - - 12162 RMVar_ID_12162 Human_SNP_ID_599309819 A-to-I Human chr16 + 29696578 29696578 29696578 GCTGAGATGGGTGGATCACGAGGTCATGAGTTAGAGACCATCCTGGCCACCATGGTGAAACGTCG GCTGAGATGGGTGGATCACGAGGTCATGAGTTGGAGACCATCCTGGCCACCATGGTGAAACGTCG A G QPRT Ensembl:ENSG00000103485 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1437247248 Functional Loss SNV dbSNP153 33..33 33 - - - 12163 RMVar_ID_12163 Human_SNP_ID_599309830 A-to-I Human chr16 + 29696616 29696616 29696616 CATCCTGGCCACCATGGTGAAACGTCGTCTCTATTAAAAATACAAAAATTAGCTGGGCATGGTGG CATCCTGGCCACCATGGTGAAACGTCGTCTCTGTTAAAAATACAAAAATTAGCTGGGCATGGTGG A G QPRT Ensembl:ENSG00000103485 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1429086338 Functional Loss SNV dbSNP153 33..33 33 - - - 12164 RMVar_ID_12164 Human_SNP_ID_599309854 A-to-I Human chr16 + 29696696 29696696 29696696 CCAGCTACTCGGGAGACTGAGGTGGGAGAATCACTTGATCCCAGGAGGTAGAGGCTGCAGTGAGC CCAGCTACTCGGGAGACTGAGGTGGGAGAATCGCTTGATCCCAGGAGGTAGAGGCTGCAGTGAGC A G QPRT Ensembl:ENSG00000103485 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170438515 Functional Loss SNV dbSNP153 33..33 33 - - - 12165 RMVar_ID_12165 Human_SNP_ID_599309952 A-to-I Human chr16 + 29697029 29697029 29697029 CGGTGCGGGCGGCCAGACAGGCGGCTGACTTCACTCTGAAGGTGGAAGTGGAATGCAGCAGCCTG CGGTGCGGGCGGCCAGACAGGCGGCTGACTTCGCTCTGAAGGTGGAAGTGGAATGCAGCAGCCTG A G QPRT Ensembl:ENSG00000103485 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs9932770 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_889606,Human_RBP_ID_9353194,Human_RBP_ID_21889201,Human_RBP_ID_22442464 Human_Splice_Rec_1699788,Human_Splice_Rec_1699789,Human_Splice_Rec_1699792,Human_Splice_Rec_1699793,Human_Splice_Rec_1699798,Human_Splice_Rec_1699799,Human_Splice_Rec_1699804,Human_Splice_Rec_1699805 12166 RMVar_ID_12166 Human_SNP_ID_599309953 A-to-I Human chr16 + 29697029 29697029 29697029 CGGTGCGGGCGGCCAGACAGGCGGCTGACTTCACTCTGAAGGTGGAAGTGGAATGCAGCAGCCTG CGGTGCGGGCGGCCAGACAGGCGGCTGACTTCTCTCTGAAGGTGGAAGTGGAATGCAGCAGCCTG A T QPRT Ensembl:ENSG00000103485 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs9932770 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_889606,Human_RBP_ID_9353194,Human_RBP_ID_21889201,Human_RBP_ID_22442464 Human_Splice_Rec_1699788,Human_Splice_Rec_1699789,Human_Splice_Rec_1699792,Human_Splice_Rec_1699793,Human_Splice_Rec_1699798,Human_Splice_Rec_1699799,Human_Splice_Rec_1699804,Human_Splice_Rec_1699805 12167 RMVar_ID_12167 Human_SNP_ID_599340442 A-to-I Human chr16 + 29807797 29807797 29807797 GCTCACATGACGGCGCTGTGCACAAGCCCTACAACTGCTCCCACTGTGGCAAGAGCTTCTCCCGG GCTCACATGACGGCGCTGTGCACAAGCCCTACCACTGCTCCCACTGTGGCAAGAGCTTCTCCCGG A C MAZ Ensembl:ENSG00000103495 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs746373999 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_1516230,Human_RBP_ID_1841118,Human_RBP_ID_3493991,Human_RBP_ID_4398469,Human_RBP_ID_6506827,Human_RBP_ID_8431761,Human_RBP_ID_9284716,Human_RBP_ID_17253844,Human_RBP_ID_17486022,Human_RBP_ID_27240061,Human_RBP_ID_27441114 Human_Splice_Rec_1699963,Human_Splice_Rec_1699971,Human_Splice_Rec_1699991,Human_Splice_Rec_1700003,Human_Splice_Rec_1700009,Human_Splice_Rec_1700013,Human_Splice_Rec_1700021 Human_miRNA_ID_1996438,Human_miRNA_ID_2228930,Human_miRNA_ID_2504907 RMVar_hsa_circ_81490,RMVar_hsa_circ_177759 12168 RMVar_ID_12168 Human_SNP_ID_599340443 A-to-I Human chr16 + 29807797 29807797 29807797 GCTCACATGACGGCGCTGTGCACAAGCCCTACAACTGCTCCCACTGTGGCAAGAGCTTCTCCCGG GCTCACATGACGGCGCTGTGCACAAGCCCTACGACTGCTCCCACTGTGGCAAGAGCTTCTCCCGG A G MAZ Ensembl:ENSG00000103495 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs746373999 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1516230,Human_RBP_ID_1841118,Human_RBP_ID_3493991,Human_RBP_ID_4398469,Human_RBP_ID_6506827,Human_RBP_ID_8431761,Human_RBP_ID_9284716,Human_RBP_ID_17253844,Human_RBP_ID_17486022,Human_RBP_ID_27240061,Human_RBP_ID_27441114 Human_Splice_Rec_1699963,Human_Splice_Rec_1699971,Human_Splice_Rec_1699991,Human_Splice_Rec_1700003,Human_Splice_Rec_1700009,Human_Splice_Rec_1700013,Human_Splice_Rec_1700021 Human_miRNA_ID_1996438,Human_miRNA_ID_2228930,Human_miRNA_ID_2504907 RMVar_hsa_circ_81490,RMVar_hsa_circ_177759 12169 RMVar_ID_12169 Human_SNP_ID_599346722 A-to-I Human chr16 + 29822741 29822740 29822742 TGCAATCGGAGCTGTGTTTTTGTTTTTGAGACAGAGTCTCGCTCTGTCCCCCAGGCCAGAGTACA TGCAATCGGAGCTGTGTTTTTGTTTTTGAGAC__AGTCTCGCTCTGTCCCCCAGGCCAGAGTACA CAG C AC120114.4,MVP Ensembl:ENSG00000281348,Ensembl:ENSG00000013364 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1007890113 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_177765,RMVar_hsa_circ_107637,RMVar_hsa_circ_80277,RMVar_hsa_circ_177764 12170 RMVar_ID_12170 Human_SNP_ID_599348156 A-to-I Human chr16 + 29827968 29827968 29827968 GTTCCTCAGATGCATTAGCCACATTTTATTTTATTTTTTTCCAAGACAGAGTCTTGCTCTGTCGC GTTCCTCAGATGCATTAGCCACATTTTATTTTTTTTTTTTCCAAGACAGAGTCTTGCTCTGTCGC A T AC120114.4,MVP Ensembl:ENSG00000281348,Ensembl:ENSG00000013364 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1353650640 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_177765,RMVar_hsa_circ_107637,RMVar_hsa_circ_80277,RMVar_hsa_circ_177764 12171 RMVar_ID_12171 Human_SNP_ID_599349914 A-to-I Human chr16 + 29834402 29834402 29834402 AATACAATTGACAAATGTAGGCCAATAGGTACAGTGGCTCACACCTGTCATCCCAGCACTTTGCC AATACAATTGACAAATGTAGGCCAATAGGTACTGTGGCTCACACCTGTCATCCCAGCACTTTGCC A T MVP Ensembl:ENSG00000013364 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,31158229,32596459 RNA-Seq:(High) rs1405412694 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1700293 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 12172 RMVar_ID_12172 Human_SNP_ID_599357718 A-to-I Human chr16 - 29861871 29861871 29861871 AAAATTAGCGGGCTTGGTGACGCGTGCCTGTAATCCCAGCTACTCGGGAGGCTAAGGCAGGAGAA AAAATTAGCGGGCTTGGTGACGCGTGCCTGTAGTCCCAGCTACTCGGGAGGCTAAGGCAGGAGAA T C CDIPT Ensembl:ENSG00000103502 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1438184052 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,RMVar_hsa_circ_86629,RMVar_hsa_circ_177780 12173 RMVar_ID_12173 Human_SNP_ID_599370607 A-to-I Human chr16 - 29907590 29907590 29907590 TAGAGATGGGGTTACACCATGTTGCCCAGACTAGACTCAAACTCCTGGCCTCAAGCTGTCCTCCC TAGAGATGGGGTTACACCATGTTGCCCAGACTGGACTCAAACTCCTGGCCTCAAGCTGTCCTCCC T C KCTD13 Ensembl:ENSG00000174943 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs945022798 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 12174 RMVar_ID_12174 Human_SNP_ID_599370637 A-to-I Human chr16 - 29907741 29907741 29907741 CACTGTCACCCAGGTTGGAGTGCAGTGGTACAATCTTGGCTCACTGCAACCTCCACCTCCCATGC CACTGTCACCCAGGTTGGAGTGCAGTGGTACAGTCTTGGCTCACTGCAACCTCCACCTCCCATGC T C KCTD13 Ensembl:ENSG00000174943 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1438345165 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 12175 RMVar_ID_12175 Human_SNP_ID_599370940 A-to-I Human chr16 - 29908919 29908919 29908919 GGAGGCTGAGGCAGGGGACCATTAAGGCCAGGAGTTTGAGGCCAGCCTGGGCAACACAGCAAGAC GGAGGCTGAGGCAGGGGACCATTAAGGCCAGGCGTTTGAGGCCAGCCTGGGCAACACAGCAAGAC T G KCTD13 Ensembl:ENSG00000174943 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027770435 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 12176 RMVar_ID_12176 Human_SNP_ID_599371295 A-to-I Human chr16 - 29910474 29910474 29910474 TTGGTGACATGATGGCATGCACCTGTAATCCCAGCTACTCAGGAAGCTAAGGCAGGAGGATTGCT TTGGTGACATGATGGCATGCACCTGTAATCCCGGCTACTCAGGAAGCTAAGGCAGGAGGATTGCT T C KCTD13 Ensembl:ENSG00000174943 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1465046746 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17564101 RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_86902,RMVar_hsa_circ_177729,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 12177 RMVar_ID_12177 Human_SNP_ID_599371328 A-to-I Human chr16 - 29910605 29910605 29910605 CCTGTAACCCCAGGACTCTGGGAGGCCAAGGCAGGAGGATCACTTGAGCCCAGGAGTTCGAGACC CCTGTAACCCCAGGACTCTGGGAGGCCAAGGCGGGAGGATCACTTGAGCCCAGGAGTTCGAGACC T C KCTD13 Ensembl:ENSG00000174943 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1188797041 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 12178 RMVar_ID_12178 Human_SNP_ID_599371334 A-to-I Human chr16 - 29910648 29910648 29910648 TTGCCATTAGAAACTCAGAAGGGGTGAGGCATAGTGGCTTACGCCTGTAACCCCAGGACTCTGGG TTGCCATTAGAAACTCAGAAGGGGTGAGGCATGGTGGCTTACGCCTGTAACCCCAGGACTCTGGG T C KCTD13 Ensembl:ENSG00000174943 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1465410401 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 12179 RMVar_ID_12179 Human_SNP_ID_599372435 A-to-I Human chr16 - 29914549 29914549 29914549 CTGTAGTCCCAGCTACTTGGGATGCTGAGGCAAGAGAATCACTTGAACCTGGGAAGCAGAGTTTT CTGTAGTCCCAGCTACTTGGGATGCTGAGGCAGGAGAATCACTTGAACCTGGGAAGCAGAGTTTT T C AC120114.3,KCTD13 Ensembl:ENSG00000279789,Ensembl:ENSG00000174943 Other,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs753843429 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5247734 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_328354,RMVar_hsa_circ_177799 12180 RMVar_ID_12180 Human_SNP_ID_599372514 A-to-I Human chr16 - 29914912 29914912 29914912 GTCTCGAACTCCTGGGCTCAAGTAATCCTCCCACCTTGGCCTCCTGAGTAGCTGGGATGACAGGC GTCTCGAACTCCTGGGCTCAAGTAATCCTCCCGCCTTGGCCTCCTGAGTAGCTGGGATGACAGGC T C AC120114.3,KCTD13 Ensembl:ENSG00000279789,Ensembl:ENSG00000174943 Other,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1262178942 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12715327,Human_RBP_ID_23686177,Human_RBP_ID_25204786 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_328354,RMVar_hsa_circ_177799 12181 RMVar_ID_12181 Human_SNP_ID_599372611 A-to-I Human chr16 - 29915395 29915395 29915395 CACCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGTGCCTGGCCACTTGCA CACCCACCTCGGCCTCCCAAAGTGCTGGGATTGCAGGCGTGAGCCACTGTGCCTGGCCACTTGCA T C KCTD13 Ensembl:ENSG00000174943 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs796392623 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,RMVar_hsa_circ_328354,RMVar_hsa_circ_177799 12182 RMVar_ID_12182 Human_SNP_ID_599373033 A-to-I Human chr16 - 29917403 29917403 29917403 AGCTCAAGCGATCTGCCCACTTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGATCCGCTATAC AGCTCAAGCGATCTGCCCACTTCGGCCTCCCAGAGTGCTGGGATTACAGGTGTGATCCGCTATAC T C KCTD13 Ensembl:ENSG00000174943 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs921950084 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,RMVar_hsa_circ_328354,RMVar_hsa_circ_177799 12183 RMVar_ID_12183 Human_SNP_ID_599373061 A-to-I Human chr16 - 29917507 29917507 29917507 AAAGTGCTGGGATTACAAGCATGAGCCACCACACCCGTCTAATTTTTGTATTTTTTGTAGAAAGG AAAGTGCTGGGATTACAAGCATGAGCCACCACCCCCGTCTAATTTTTGTATTTTTTGTAGAAAGG T G KCTD13 Ensembl:ENSG00000174943 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1303020923 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,RMVar_hsa_circ_328354,RMVar_hsa_circ_177799 12184 RMVar_ID_12184 Human_SNP_ID_599373189 A-to-I Human chr16 - 29918086 29918086 29918086 AGATTATTTGTAAAGTCATGCTTTCCATTGTCAACTTGAAAAATTCTTGATTTGGATGTAGTCCA AGATTATTTGTAAAGTCATGCTTTCCATTGTCGACTTGAAAAATTCTTGATTTGGATGTAGTCCA T C KCTD13 Ensembl:ENSG00000174943 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941366796 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,RMVar_hsa_circ_328354,RMVar_hsa_circ_177799 12185 RMVar_ID_12185 Human_SNP_ID_599373195 A-to-I Human chr16 - 29918107 29918107 29918107 TCTCTTCAACATTATTACATGAGATTATTTGTAAAGTCATGCTTTCCATTGTCAACTTGAAAAAT TCTCTTCAACATTATTACATGAGATTATTTGTGAAGTCATGCTTTCCATTGTCAACTTGAAAAAT T C KCTD13 Ensembl:ENSG00000174943 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1458290006 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12715432 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_328354,RMVar_hsa_circ_177799 12186 RMVar_ID_12186 Human_SNP_ID_599373479 A-to-I Human chr16 - 29919446 29919446 29919446 GTTGAAGAGATGATAAGAGTTATAGGTATTCTATGGCACGAATGTAATTACTGGTTCAGGTAAGG GTTGAAGAGATGATAAGAGTTATAGGTATTCTGTGGCACGAATGTAATTACTGGTTCAGGTAAGG T C KCTD13 Ensembl:ENSG00000174943 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs949869639 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,RMVar_hsa_circ_328354,RMVar_hsa_circ_177799 12187 RMVar_ID_12187 Human_SNP_ID_599373483 A-to-I Human chr16 - 29919457 29919457 29919457 CATGTAATAATGTTGAAGAGATGATAAGAGTTATAGGTATTCTATGGCACGAATGTAATTACTGG CATGTAATAATGTTGAAGAGATGATAAGAGTTTTAGGTATTCTATGGCACGAATGTAATTACTGG T A KCTD13 Ensembl:ENSG00000174943 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs769276140 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2472922 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_328354,RMVar_hsa_circ_177799 12188 RMVar_ID_12188 Human_SNP_ID_599373484 A-to-I Human chr16 - 29919457 29919457 29919457 CATGTAATAATGTTGAAGAGATGATAAGAGTTATAGGTATTCTATGGCACGAATGTAATTACTGG CATGTAATAATGTTGAAGAGATGATAAGAGTTGTAGGTATTCTATGGCACGAATGTAATTACTGG T C KCTD13 Ensembl:ENSG00000174943 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs769276140 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2472922 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_328354,RMVar_hsa_circ_177799 12189 RMVar_ID_12189 Human_SNP_ID_599373488 A-to-I Human chr16 - 29919494 29919494 29919494 AAGTTAACAATGGAAAGCATGACTTTACAAATAGTTTCATGTAATAATGTTGAAGAGATGATAAG AAGTTAACAATGGAAAGCATGACTTTACAAATGGTTTCATGTAATAATGTTGAAGAGATGATAAG T C KCTD13 Ensembl:ENSG00000174943 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1038261210 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8431884 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_328354,RMVar_hsa_circ_177799 12190 RMVar_ID_12190 Human_SNP_ID_599374065 A-to-I Human chr16 - 29921961 29921959 29921961 CTCTGTAGCATTTTTGTTTTGTTTTGAGACAGAGTCTCTCTGTCGCCCAGGCTGGAGTGCAATGG CTCTGTAGCATTTTTGTTTTGTTTTGAGACAG__TCTCTCTGTCGCCCAGGCTGGAGTGCAATGG ACT A KCTD13 Ensembl:ENSG00000174943 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1300704494 Functional Loss DEL dbSNP153 33..34 33 - - - Human_Splice_Rec_1700692,Human_Splice_Rec_1700698 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_328354,RMVar_hsa_circ_177799 12191 RMVar_ID_12191 Human_SNP_ID_599374583 A-to-I Human chr16 - 29923807 29923807 29923807 TCTTATTACCCAGGCTGGAGTGCAATGGCGCGATCTCGGCTCACTGCAAACTCCACCTCCCGGCT TCTTATTACCCAGGCTGGAGTGCAATGGCGCGGTCTCGGCTCACTGCAAACTCCACCTCCCGGCT T C KCTD13 Ensembl:ENSG00000174943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs922178981 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,RMVar_hsa_circ_177801,RMVar_hsa_circ_127286 12192 RMVar_ID_12192 Human_SNP_ID_599376352 A-to-I Human chr16 + 29930501 29930501 29930501 GACCTCAGGTGATCCACCCACCTCTGGCTCCCAAAGTGTTGGGATTACAGGCATGAGCCACCACG GACCTCAGGTGATCCACCCACCTCTGGCTCCCGAAGTGTTGGGATTACAGGCATGAGCCACCACG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1429611444 Functional Loss SNV dbSNP153 33..33 33 - - - 12193 RMVar_ID_12193 Human_SNP_ID_599376488 A-to-I Human chr16 + 29931178 29931178 29931178 AAAATCAGCCAGGCTTGGTGGTGCGCACCTGTAATCCCAGCTACTTTGGAGGCTGAAGCAGGAGA AAAATCAGCCAGGCTTGGTGGTGCGCACCTGTGATCCCAGCTACTTTGGAGGCTGAAGCAGGAGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1294554028 Functional Loss SNV dbSNP153 33..33 33 - - - 12194 RMVar_ID_12194 Human_SNP_ID_599376495 A-to-I Human chr16 + 29931201 29931201 29931201 CGCACCTGTAATCCCAGCTACTTTGGAGGCTGAAGCAGGAGAATTGTTTGAGTCCATGAAGTGGA CGCACCTGTAATCCCAGCTACTTTGGAGGCTGTAGCAGGAGAATTGTTTGAGTCCATGAAGTGGA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1306731287 Functional Loss SNV dbSNP153 33..33 33 - - - 12195 RMVar_ID_12195 Human_SNP_ID_599376499 A-to-I Human chr16 + 29931227 29931227 29931227 AGGCTGAAGCAGGAGAATTGTTTGAGTCCATGAAGTGGAGGCTACAGTGAACTGAGATCATGCCA AGGCTGAAGCAGGAGAATTGTTTGAGTCCATGCAGTGGAGGCTACAGTGAACTGAGATCATGCCA A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1040433976 Functional Loss SNV dbSNP153 33..33 33 - - - 12196 RMVar_ID_12196 Human_SNP_ID_61916 A-to-I Human chr1 + 630560 630560 630560 ATCTACTCCACCTCAATCACACTACTCCCTATATCTAACAACGTAAAAATAAAATGACAGTTTGA ATCTACTCCACCTCAATCACACTACTCCCTATGTCTAACAACGTAAAAATAAAATGACAGTTTGA A G MTND2P28 Ensembl:ENSG00000225630 Pseudogene exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs561754958 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8240924,Human_RBP_ID_8315248,Human_RBP_ID_17182054,Human_RBP_ID_18509550,Human_RBP_ID_18523873 12197 RMVar_ID_12197 Human_SNP_ID_76608 A-to-I Human chr1 - 727280 727280 727280 GGACAGAGGTCAGCGTGAGCCCCTTGTCTCACACCGGCCCCTCCCACGCTGAGAGAGGTCAATGT GGACAGAGGTCAGCGTGAGCCCCTTGTCTCACGCCGGCCCCTCCCACGCTGAGAGAGGTCAATGT T C AL669831.1,AL669831.3 Ensembl:ENSG00000228327,Ensembl:ENSG00000230021 Pseudogene,Pseudogene exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1487057643 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223403,Human_RBP_ID_17556460,Human_RBP_ID_22369450,Human_RBP_ID_26753539 12198 RMVar_ID_12198 Human_SNP_ID_95322 A-to-I Human chr1 - 810172 810172 810172 AAAAATATTTTAATAGAATATGTCTTTATTTCAGTATCTTAAATAGTGAAGATGGAGAAATAGTC AAAAATATTTTAATAGAATATGTCTTTATTTCTGTATCTTAAATAGTGAAGATGGAGAAATAGTC T A AL669831.4,AL669831.3 Ensembl:ENSG00000230092,Ensembl:ENSG00000230021 Pseudogene,Pseudogene intron,intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1335434113 Functional Loss SNV dbSNP153 33..33 33 - - - 12199 RMVar_ID_12199 Human_SNP_ID_138283 A-to-I Human chr1 + 944234 944230 944234 CTCAACACAATGGCCCTGCCTCCCACCGCTTTATTTCTTTCGGTTTCGGATGCAAAACAAAAAAT CTCAACACAATGGCCCTGCCTCCCACCGC____TTTCTTTCGGTTTCGGATGCAAAACAAAAAAT CTTTA C SAMD11 Ensembl:ENSG00000187634 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs961980926 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_23302,Human_RBP_ID_1755682,Human_RBP_ID_3324418,Human_RBP_ID_17337506,Human_RBP_ID_18582309,Human_RBP_ID_22147822,Human_RBP_ID_26383889,Human_RBP_ID_26870887,Human_RBP_ID_27187185 RMVar_hsa_circ_117918,RMVar_hsa_circ_128235 12200 RMVar_ID_12200 Human_SNP_ID_138285 A-to-I Human chr1 + 944234 944234 944234 CTCAACACAATGGCCCTGCCTCCCACCGCTTTATTTCTTTCGGTTTCGGATGCAAAACAAAAAAT CTCAACACAATGGCCCTGCCTCCCACCGCTTTCTTTCTTTCGGTTTCGGATGCAAAACAAAAAAT A C SAMD11 Ensembl:ENSG00000187634 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs544040354 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23302,Human_RBP_ID_1755682,Human_RBP_ID_3324418,Human_RBP_ID_17337506,Human_RBP_ID_18582309,Human_RBP_ID_22147822,Human_RBP_ID_26383889,Human_RBP_ID_26870887,Human_RBP_ID_27187185 RMVar_hsa_circ_117918,RMVar_hsa_circ_128235 12201 RMVar_ID_12201 Human_SNP_ID_138302 A-to-I Human chr1 + 944270 944270 944270 CTTTCGGTTTCGGATGCAAAACAAAAAATTTTAAAAGAAAATGTGACTTCAAAGGAAAGGAACAA CTTTCGGTTTCGGATGCAAAACAAAAAATTTTTAAAGAAAATGTGACTTCAAAGGAAAGGAACAA A T SAMD11 Ensembl:ENSG00000187634 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs911961517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1755686,Human_RBP_ID_8050535,Human_RBP_ID_18582312,Human_RBP_ID_22147822 RMVar_hsa_circ_117918,RMVar_hsa_circ_128235 12202 RMVar_ID_12202 Human_SNP_ID_138463 A-to-I Human chr1 - 944539 944539 944539 GCTTTATTATTTATTTTTCAGCATGAAAGACCAAACGTATCGAGAGCTGGGCTGGGCTGGGCTGG GCTTTATTATTTATTTTTCAGCATGAAAGACCGAACGTATCGAGAGCTGGGCTGGGCTGGGCTGG T C NOC2L Ensembl:ENSG00000188976 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs28453979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_258300,Human_RBP_ID_364541,Human_RBP_ID_1755687,Human_RBP_ID_11135239,Human_RBP_ID_17763246,Human_RBP_ID_18186683,Human_RBP_ID_18964337,Human_RBP_ID_22557392,Human_RBP_ID_24454603,Human_RBP_ID_26385004 Human_miRNA_ID_244822,Human_miRNA_ID_247324 12203 RMVar_ID_12203 Human_SNP_ID_138464 A-to-I Human chr1 - 944539 944539 944539 GCTTTATTATTTATTTTTCAGCATGAAAGACCAAACGTATCGAGAGCTGGGCTGGGCTGGGCTGG GCTTTATTATTTATTTTTCAGCATGAAAGACCCAACGTATCGAGAGCTGGGCTGGGCTGGGCTGG T G NOC2L Ensembl:ENSG00000188976 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs28453979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_258300,Human_RBP_ID_364541,Human_RBP_ID_1755687,Human_RBP_ID_11135239,Human_RBP_ID_17763246,Human_RBP_ID_18186683,Human_RBP_ID_18964337,Human_RBP_ID_22557392,Human_RBP_ID_24454603,Human_RBP_ID_26385004 Human_miRNA_ID_244822,Human_miRNA_ID_247324 12204 RMVar_ID_12204 Human_SNP_ID_197258 A-to-I Human chr1 - 1094209 1094209 1094209 CCTGTAGTCTCAGCTACTCGGGAGGCTGATGTAGGAGTATCGCGTAAGCCCTGGAGGTCAAGGCT CCTGTAGTCTCAGCTACTCGGGAGGCTGATGTCGGAGTATCGCGTAAGCCCTGGAGGTCAAGGCT T G C1orf159 Ensembl:ENSG00000131591 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs545310884 Functional Loss SNV dbSNP153 33..33 33 - - - 12205 RMVar_ID_12205 Human_SNP_ID_197329 A-to-I Human chr1 - 1094490 1094490 1094490 AGGCTGAGGCAGGAGAATGGTGTGAACCCAGAAGGCGGGGCTTGCAGTGAACTGAGATCACGCCA AGGCTGAGGCAGGAGAATGGTGTGAACCCAGACGGCGGGGCTTGCAGTGAACTGAGATCACGCCA T G C1orf159 Ensembl:ENSG00000131591 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs981920110 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22557438,Human_RBP_ID_22706772 12206 RMVar_ID_12206 Human_SNP_ID_197728 A-to-I Human chr1 - 1096277 1096277 1096277 AGGTGGGAGGATCCCTTGATCCCAGGAGCTCAAGGCGGCAGTGAGCCATGATCGCACCACTACAC AGGTGGGAGGATCCCTTGATCCCAGGAGCTCATGGCGGCAGTGAGCCATGATCGCACCACTACAC T A C1orf159 Ensembl:ENSG00000131591 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1229057477 Functional Loss SNV dbSNP153 33..33 33 - - - 12207 RMVar_ID_12207 Human_SNP_ID_199583 A-to-I Human chr1 - 1102536 1102536 1102536 ACCTCAGGTGATCCACCTACCTCAGCCTCTCAAGGTGCTGGGATTACAGGCGTGAGCCACTGTGC ACCTCAGGTGATCCACCTACCTCAGCCTCTCAGGGTGCTGGGATTACAGGCGTGAGCCACTGTGC T C C1orf159 Ensembl:ENSG00000131591 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs535996620 Functional Loss SNV dbSNP153 33..33 33 - - - 12208 RMVar_ID_12208 Human_SNP_ID_199585 A-to-I Human chr1 - 1102545 1102545 1102545 CTTGAACTGACCTCAGGTGATCCACCTACCTCAGCCTCTCAAGGTGCTGGGATTACAGGCGTGAG CTTGAACTGACCTCAGGTGATCCACCTACCTCGGCCTCTCAAGGTGCTGGGATTACAGGCGTGAG T C C1orf159 Ensembl:ENSG00000131591 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1160947267 Functional Loss SNV dbSNP153 33..33 33 - - - 12209 RMVar_ID_12209 Human_SNP_ID_199586 A-to-I Human chr1 - 1102563 1102563 1102563 TATGTTGGCCAGGCTTGTCTTGAACTGACCTCAGGTGATCCACCTACCTCAGCCTCTCAAGGTGC TATGTTGGCCAGGCTTGTCTTGAACTGACCTCGGGTGATCCACCTACCTCAGCCTCTCAAGGTGC T C C1orf159 Ensembl:ENSG00000131591 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1412166041 Functional Loss SNV dbSNP153 33..33 33 - - - 12210 RMVar_ID_12210 Human_SNP_ID_202798 A-to-I Human chr1 - 1113254 1113254 1113254 CGGCCTCGATTCTCGCTGCCTCAGAAGAAAGAATTTGATGGAAGGACATGAGGCTGAAGGAGAGA CGGCCTCGATTCTCGCTGCCTCAGAAGAAAGATTTTGATGGAAGGACATGAGGCTGAAGGAGAGA T A C1orf159 Ensembl:ENSG00000131591 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1056100493 Functional Loss SNV dbSNP153 33..33 33 - - - 12211 RMVar_ID_12211 Human_SNP_ID_202799 A-to-I Human chr1 - 1113254 1113254 1113254 CGGCCTCGATTCTCGCTGCCTCAGAAGAAAGAATTTGATGGAAGGACATGAGGCTGAAGGAGAGA CGGCCTCGATTCTCGCTGCCTCAGAAGAAAGAGTTTGATGGAAGGACATGAGGCTGAAGGAGAGA T C C1orf159 Ensembl:ENSG00000131591 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1056100493 Functional Loss SNV dbSNP153 33..33 33 - - - 12212 RMVar_ID_12212 Human_SNP_ID_202802 A-to-I Human chr1 - 1113261 1113261 1113261 TCAGCAGCGGCCTCGATTCTCGCTGCCTCAGAAGAAAGAATTTGATGGAAGGACATGAGGCTGAA TCAGCAGCGGCCTCGATTCTCGCTGCCTCAGACGAAAGAATTTGATGGAAGGACATGAGGCTGAA T G C1orf159 Ensembl:ENSG00000131591 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1166593626 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23142973 12213 RMVar_ID_12213 Human_SNP_ID_202816 A-to-I Human chr1 - 1113318 1113318 1113318 GAGCCTTCAGAGCTCTATTACTGGCAGAATGTATCTGAGTTTCAGCACCAAAGTATGTCAGCAGC GAGCCTTCAGAGCTCTATTACTGGCAGAATGTGTCTGAGTTTCAGCACCAAAGTATGTCAGCAGC T C C1orf159 Ensembl:ENSG00000131591 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1029046619 Functional Loss SNV dbSNP153 33..33 33 - - - 12214 RMVar_ID_12214 Human_SNP_ID_237553 A-to-I Human chr1 - 1217639 1217639 1217639 GAACGAGTACAACGCGCTGAACGAGGCCAAGCAGATGATCGCCGTCGCCGACGAGAACCAGAACC GAACGAGTACAACGCGCTGAACGAGGCCAAGCGGATGATCGCCGTCGCCGACGAGAACCAGAACC T C SDF4 Ensembl:ENSG00000078808 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1313077091 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_322499,Human_RBP_ID_741651,Human_RBP_ID_5536331,Human_RBP_ID_8282035,Human_RBP_ID_10538956,Human_RBP_ID_17211557,Human_RBP_ID_26315722,Human_RBP_ID_26366478 Human_Splice_Rec_2102,Human_Splice_Rec_2142,Human_Splice_Rec_2144 RMVar_hsa_circ_101468,RMVar_hsa_circ_128285 12215 RMVar_ID_12215 Human_SNP_ID_244125 A-to-I Human chr1 + 1234812 1234812 1234812 TTGGAGAGGCCAGAGGGCTTGCTGAGAACCCCATGGACAGTGGAGAGCGGGATTCGAACCAAGGG TTGGAGAGGCCAGAGGGCTTGCTGAGAACCCCGTGGACAGTGGAGAGCGGGATTCGAACCAAGGG A G B3GALT6 Ensembl:ENSG00000176022 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs372447529 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2088633,Human_RBP_ID_8282228 12216 RMVar_ID_12216 Human_SNP_ID_250776 A-to-I Human chr1 - 1252787 1252787 1252787 GGAGCCCGGTGTACAGGGCGGACCACGAAAGCAGACCAGGAGTGTGACCGCTGAAGCACAGCATC GGAGCCCGGTGTACAGGGCGGACCACGAAAGCGGACCAGGAGTGTGACCGCTGAAGCACAGCATC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1011228082 Functional Loss SNV dbSNP153 33..33 33 - - - 12217 RMVar_ID_12217 Human_SNP_ID_250919 A-to-I Human chr1 - 1253149 1253149 1253149 GGTTCTTCTTGTGTACGGAGAGATGTGAGATCATAGAAATAAAGACACAAGACAGGGATAGAAGA GGTTCTTCTTGTGTACGGAGAGATGTGAGATCCTAGAAATAAAGACACAAGACAGGGATAGAAGA T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1176759470 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10544715 12218 RMVar_ID_12218 Human_SNP_ID_250953 A-to-I Human chr1 - 1253236 1253236 1253236 GTCTTGCTCTGTTGTTGCCCAGTGTGGAGTGCAATGGTGCTATCATGGCTCCCTGTAACTGCAGG GTCTTGCTCTGTTGTTGCCCAGTGTGGAGTGCGATGGTGCTATCATGGCTCCCTGTAACTGCAGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs551528178 Functional Loss SNV dbSNP153 33..33 33 - - - 12219 RMVar_ID_12219 Human_SNP_ID_250954 A-to-I Human chr1 - 1253236 1253236 1253236 GTCTTGCTCTGTTGTTGCCCAGTGTGGAGTGCAATGGTGCTATCATGGCTCCCTGTAACTGCAGG GTCTTGCTCTGTTGTTGCCCAGTGTGGAGTGCCATGGTGCTATCATGGCTCCCTGTAACTGCAGG T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs551528178 Functional Loss SNV dbSNP153 33..33 33 - - - 12220 RMVar_ID_12220 Human_SNP_ID_254815 A-to-I Human chr1 - 1264832 1264832 1264832 GTGACCTCGGCTCACTGCAACCTCCGTCTTCCAGGTTCAAGCGATTCTCCTGGCTCAGCCTCCTG GTGACCTCGGCTCACTGCAACCTCCGTCTTCCGGGTTCAAGCGATTCTCCTGGCTCAGCCTCCTG T C UBE2J2 Ensembl:ENSG00000160087 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) - Functional Loss SNV HGVD 33..33 33 - - - Human_Splice_Rec_2261,Human_Splice_Rec_2349 RMVar_hsa_circ_3575,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_8324,RMVar_hsa_circ_324070,RMVar_hsa_circ_277770,RMVar_hsa_circ_128301 12221 RMVar_ID_12221 Human_SNP_ID_254816 A-to-I Human chr1 - 1264832 1264832 1264832 GTGACCTCGGCTCACTGCAACCTCCGTCTTCCAGGTTCAAGCGATTCTCCTGGCTCAGCCTCCTG GTGACCTCGGCTCACTGCAACCTCCGTCTTCCCGGTTCAAGCGATTCTCCTGGCTCAGCCTCCTG T G UBE2J2 Ensembl:ENSG00000160087 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) - Functional Loss SNV HGVD 33..33 33 - - - Human_Splice_Rec_2261,Human_Splice_Rec_2349 RMVar_hsa_circ_3575,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_8324,RMVar_hsa_circ_324070,RMVar_hsa_circ_277770,RMVar_hsa_circ_128301 12222 RMVar_ID_12222 Human_SNP_ID_255183 A-to-I Human chr1 - 1265724 1265724 1265724 ACTTGGGAGGGTGAGGCAGGAGAATCGCTTGAACCCGGGAAGCGGAGGTTGCAGTGAGCTGAGAT ACTTGGGAGGGTGAGGCAGGAGAATCGCTTGATCCCGGGAAGCGGAGGTTGCAGTGAGCTGAGAT T A UBE2J2 Ensembl:ENSG00000160087 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1242485948 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3575,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_8324,RMVar_hsa_circ_324070,RMVar_hsa_circ_277770,RMVar_hsa_circ_128301 12223 RMVar_ID_12223 Human_SNP_ID_255539 A-to-I Human chr1 - 1266705 1266705 1266705 CTCTGGCCTCAGTTTCCCAAGTAGCTGGGACTACAGGCGCCTGCCACCATGCCCGGCTAATTTTT CTCTGGCCTCAGTTTCCCAAGTAGCTGGGACTCCAGGCGCCTGCCACCATGCCCGGCTAATTTTT T G UBE2J2 Ensembl:ENSG00000160087 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs987849601 Functional Loss SNV dbSNP153 33..33 33 - - - 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_128301 12224 RMVar_ID_12224 Human_SNP_ID_255543 A-to-I Human chr1 - 1266719 1266719 1266719 GGGTTCATGCCATTCTCTGGCCTCAGTTTCCCAAGTAGCTGGGACTACAGGCGCCTGCCACCATG GGGTTCATGCCATTCTCTGGCCTCAGTTTCCCGAGTAGCTGGGACTACAGGCGCCTGCCACCATG T C UBE2J2 Ensembl:ENSG00000160087 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs926387973 Functional Loss SNV dbSNP153 33..33 33 - - - 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_128301 12225 RMVar_ID_12225 Human_SNP_ID_255640 A-to-I Human chr1 - 1267042 1267042 1267042 TCTACTAAAAATACAAATATTAGCTGGGCATGATGGCGCACACCTGTAGTCCCAGCTACTCGGGA TCTACTAAAAATACAAATATTAGCTGGGCATGGTGGCGCACACCTGTAGTCCCAGCTACTCGGGA T C UBE2J2 Ensembl:ENSG00000160087 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1168454152 Functional Loss SNV dbSNP153 33..33 33 - - - 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_128301 12226 RMVar_ID_12226 Human_SNP_ID_259758 A-to-I Human chr1 + 1280123 1280123 1280123 CCGAGGCAGGCGGATCACCAGGTCAAGAGATCAAGACCAGCCTGGCCAATATGGTGAAACCCCAT CCGAGGCAGGCGGATCACCAGGTCAAGAGATCGAGACCAGCCTGGCCAATATGGTGAAACCCCAT A G LINC01786 Ensembl:ENSG00000230415 lincRNA intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1336143183 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128303 12227 RMVar_ID_12227 Human_SNP_ID_277858 A-to-I Human chr1 + 1316379 1316379 1316379 GGGAGACCAAGGTGGGCAGATCATCTGAAGTCAGGAGTTCAAGACCATCCTGGCCGACACGGTGA GGGAGACCAAGGTGGGCAGATCATCTGAAGTCTGGAGTTCAAGACCATCCTGGCCGACACGGTGA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277292413 Functional Loss SNV dbSNP153 33..33 33 - - - 12228 RMVar_ID_12228 Human_SNP_ID_277884 A-to-I Human chr1 - 1316464 1316464 1316464 CTGCCTTAGCCTACTGAGTAGCTGGGATTACAAGCACCCACCACCATGCCCAGCTAACTTTTGTA CTGCCTTAGCCTACTGAGTAGCTGGGATTACATGCACCCACCACCATGCCCAGCTAACTTTTGTA T A INTS11 Ensembl:ENSG00000127054 Protein coding intron GSE47997;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,31158229,32596459 RNA-Seq:(High) rs997366674 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28672,RMVar_hsa_circ_55849 12229 RMVar_ID_12229 Human_SNP_ID_277885 A-to-I Human chr1 - 1316464 1316464 1316464 CTGCCTTAGCCTACTGAGTAGCTGGGATTACAAGCACCCACCACCATGCCCAGCTAACTTTTGTA CTGCCTTAGCCTACTGAGTAGCTGGGATTACAGGCACCCACCACCATGCCCAGCTAACTTTTGTA T C INTS11 Ensembl:ENSG00000127054 Protein coding intron GSE47997;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,31158229,32596459 RNA-Seq:(High) rs997366674 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28672,RMVar_hsa_circ_55849 12230 RMVar_ID_12230 Human_SNP_ID_277887 A-to-I Human chr1 - 1316467 1316467 1316467 ATTCTGCCTTAGCCTACTGAGTAGCTGGGATTACAAGCACCCACCACCATGCCCAGCTAACTTTT ATTCTGCCTTAGCCTACTGAGTAGCTGGGATTGCAAGCACCCACCACCATGCCCAGCTAACTTTT T C INTS11 Ensembl:ENSG00000127054 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs144848405 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28672,RMVar_hsa_circ_55849 12231 RMVar_ID_12231 Human_SNP_ID_277910 A-to-I Human chr1 - 1316534 1316534 1316534 TTGCCCAGGCTGGAGTGCAATGGCACAATCTCAGCTCACTGCAATCTCCGCCTCCCGGGTTCAAG TTGCCCAGGCTGGAGTGCAATGGCACAATCTCGGCTCACTGCAATCTCCGCCTCCCGGGTTCAAG T C INTS11 Ensembl:ENSG00000127054 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1423735310 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28672,RMVar_hsa_circ_55849 12232 RMVar_ID_12232 Human_SNP_ID_277914 A-to-I Human chr1 - 1316547 1316547 1316547 ACTCTCGCTCTTGTTGCCCAGGCTGGAGTGCAATGGCACAATCTCAGCTCACTGCAATCTCCGCC ACTCTCGCTCTTGTTGCCCAGGCTGGAGTGCAGTGGCACAATCTCAGCTCACTGCAATCTCCGCC T C INTS11 Ensembl:ENSG00000127054 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1414877662 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11181493,Human_RBP_ID_24751031,Human_RBP_ID_26839656 RMVar_hsa_circ_28672,RMVar_hsa_circ_55849 12233 RMVar_ID_12233 Human_SNP_ID_277985 A-to-I Human chr1 - 1316792 1316792 1316792 AGCCTCCCGAGTAGCTGGGATTACAGGCGCACACCACCACATCCGGCTAATTTTGTATTTTTAGT AGCCTCCCGAGTAGCTGGGATTACAGGCGCACGCCACCACATCCGGCTAATTTTGTATTTTTAGT T C INTS11 Ensembl:ENSG00000127054 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1349392182 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5681358 RMVar_hsa_circ_28672,RMVar_hsa_circ_55849 12234 RMVar_ID_12234 Human_SNP_ID_277986 A-to-I Human chr1 - 1316794 1316794 1316794 TCAGCCTCCCGAGTAGCTGGGATTACAGGCGCACACCACCACATCCGGCTAATTTTGTATTTTTA TCAGCCTCCCGAGTAGCTGGGATTACAGGCGCGCACCACCACATCCGGCTAATTTTGTATTTTTA T C INTS11 Ensembl:ENSG00000127054 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs554287368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5681358 RMVar_hsa_circ_28672,RMVar_hsa_circ_55849 12235 RMVar_ID_12235 Human_SNP_ID_277987 A-to-I Human chr1 - 1316794 1316794 1316794 TCAGCCTCCCGAGTAGCTGGGATTACAGGCGCACACCACCACATCCGGCTAATTTTGTATTTTTA TCAGCCTCCCGAGTAGCTGGGATTACAGGCGCCCACCACCACATCCGGCTAATTTTGTATTTTTA T G INTS11 Ensembl:ENSG00000127054 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs554287368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5681358 RMVar_hsa_circ_28672,RMVar_hsa_circ_55849 12236 RMVar_ID_12236 Human_SNP_ID_278103 A-to-I Human chr1 - 1317061 1317060 1317062 AAATTAGCCTGGCGTGGTGGGTGCGTGCCTATAGTCCCAGCTATTTGGGAGGCGGAGGTGGAGGC AAATTAGCCTGGCGTGGTGGGTGCGTGCCTA__GTCCCAGCTATTTGGGAGGCGGAGGTGGAGGC CTA C INTS11 Ensembl:ENSG00000127054 Protein coding intron GSE47997;GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1307091249 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_10553829,Human_RBP_ID_17556835,Human_RBP_ID_22845749,Human_RBP_ID_23143607,Human_RBP_ID_26367160 RMVar_hsa_circ_28672,RMVar_hsa_circ_55849 12237 RMVar_ID_12237 Human_SNP_ID_278104 A-to-I Human chr1 - 1317061 1317061 1317061 AAATTAGCCTGGCGTGGTGGGTGCGTGCCTATAGTCCCAGCTATTTGGGAGGCGGAGGTGGAGGC AAATTAGCCTGGCGTGGTGGGTGCGTGCCTATGGTCCCAGCTATTTGGGAGGCGGAGGTGGAGGC T C INTS11 Ensembl:ENSG00000127054 Protein coding intron GSE47997;GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1225563597 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10553829,Human_RBP_ID_17556835,Human_RBP_ID_22845749,Human_RBP_ID_23143607,Human_RBP_ID_26367160 RMVar_hsa_circ_28672,RMVar_hsa_circ_55849 12238 RMVar_ID_12238 Human_SNP_ID_278106 A-to-I Human chr1 - 1317063 1317063 1317063 TTAAATTAGCCTGGCGTGGTGGGTGCGTGCCTATAGTCCCAGCTATTTGGGAGGCGGAGGTGGAG TTAAATTAGCCTGGCGTGGTGGGTGCGTGCCTGTAGTCCCAGCTATTTGGGAGGCGGAGGTGGAG T C INTS11 Ensembl:ENSG00000127054 Protein coding intron GSE47997;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs535801659 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10553829,Human_RBP_ID_17556835,Human_RBP_ID_22845749,Human_RBP_ID_23143607,Human_RBP_ID_24579717,Human_RBP_ID_26367160 RMVar_hsa_circ_28672,RMVar_hsa_circ_55849 12239 RMVar_ID_12239 Human_SNP_ID_278413 A-to-I Human chr1 - 1318006 1318006 1318006 AAAAATTAGCTGGGCGTGGTGCGGGCGCCTGCAGTCCCAGCTACTCGGGAGGCTGAAAGGCAGGA AAAAATTAGCTGGGCGTGGTGCGGGCGCCTGCCGTCCCAGCTACTCGGGAGGCTGAAAGGCAGGA T G INTS11,AL139287.1 Ensembl:ENSG00000127054,Ensembl:ENSG00000240731 Protein coding,lincRNA intron,intron GSE38233;GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,30559470,31158229 RNA-Seq:(High) rs569606583 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_99620,Human_RBP_ID_8243371 RMVar_hsa_circ_28672,RMVar_hsa_circ_55849 12240 RMVar_ID_12240 Human_SNP_ID_278571 A-to-I Human chr1 - 1318564 1318564 1318564 AGCCTCGGCCTCCCGGGTTGAGGTGATCTCCCACCTCGGCCTCCCAAGTAGCTGGGACTACAAGC AGCCTCGGCCTCCCGGGTTGAGGTGATCTCCCGCCTCGGCCTCCCAAGTAGCTGGGACTACAAGC T C INTS11,AL139287.1 Ensembl:ENSG00000127054,Ensembl:ENSG00000240731 Protein coding,lincRNA intron,intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 31158229,32596459,32596459 RNA-Seq:(High) rs978867684 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5245533,Human_RBP_ID_10553976 RMVar_hsa_circ_28672,RMVar_hsa_circ_55849 12241 RMVar_ID_12241 Human_SNP_ID_278572 A-to-I Human chr1 - 1318576 1318576 1318576 TTGGCTCACTGCAGCCTCGGCCTCCCGGGTTGAGGTGATCTCCCACCTCGGCCTCCCAAGTAGCT TTGGCTCACTGCAGCCTCGGCCTCCCGGGTTGGGGTGATCTCCCACCTCGGCCTCCCAAGTAGCT T C INTS11,AL139287.1 Ensembl:ENSG00000127054,Ensembl:ENSG00000240731 Protein coding,lincRNA intron,intron GSE100210;GSE107867 HepG2 cell line;ASD brains,cerebellum - 29129909,30559470 RNA-Seq:(High) rs1372008701 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5245533,Human_RBP_ID_10553976 RMVar_hsa_circ_28672,RMVar_hsa_circ_55849 12242 RMVar_ID_12242 Human_SNP_ID_278592 A-to-I Human chr1 - 1318636 1318636 1318636 CTTTAATTTTTTTTTTTTTTTGACAGTGTCTCACTTTGTTACCCAGGCTGGAGTGTGATCTTGGC CTTTAATTTTTTTTTTTTTTTGACAGTGTCTCCCTTTGTTACCCAGGCTGGAGTGTGATCTTGGC T G INTS11,AL139287.1 Ensembl:ENSG00000127054,Ensembl:ENSG00000240731 Protein coding,lincRNA intron,exon GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs1210080798 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5245533,Human_RBP_ID_10553978,Human_RBP_ID_17556836 RMVar_hsa_circ_28672,RMVar_hsa_circ_55849 12243 RMVar_ID_12243 Human_SNP_ID_293141 A-to-I Human chr1 - 1349663 1349663 1349663 GCCTTCGCGGTGGCGCAGAGCGACCGGGCGCCACCTCAGCGCCGCGCACCCGGCGTCCCCGGGGT GCCTTCGCGGTGGCGCAGAGCGACCGGGCGCCTCCTCAGCGCCGCGCACCCGGCGTCCCCGGGGT T A - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1309018027 Functional Loss SNV dbSNP153 33..33 33 - - - 12244 RMVar_ID_12244 Human_SNP_ID_310063 A-to-I Human chr1 - 1396541 1396541 1396541 AACAGCCTTGCCGAGCGCAGTGGCTCACGCCTATAGTCCCAGCACTTTGGGAGGCCAAGGCGGGT AACAGCCTTGCCGAGCGCAGTGGCTCACGCCTGTAGTCCCAGCACTTTGGGAGGCCAAGGCGGGT T C CCNL2 Ensembl:ENSG00000221978 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1213929473 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54913,RMVar_hsa_circ_299083,RMVar_hsa_circ_128326 12245 RMVar_ID_12245 Human_SNP_ID_312822 A-to-I Human chr1 - 1402811 1402811 1402811 TGGTTTTTTTTCTTGTATTTTTTAGTACAGACAGGGTTTCTCCATGTTGGTCAGACTAGTCTCGA TGGTTTTTTTTCTTGTATTTTTTAGTACAGACGGGGTTTCTCCATGTTGGTCAGACTAGTCTCGA T C MRPL20 Ensembl:ENSG00000242485 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs976910321 Functional Loss SNV dbSNP153 33..33 33 - - - 12246 RMVar_ID_12246 Human_SNP_ID_313248 A-to-I Human chr1 - 1404035 1404035 1404035 CAGGAGTTCGACAGCAGCCTGGGCAATGTGGTAAAACTCTGTCTCTATTCAAAATACAAAATGAG CAGGAGTTCGACAGCAGCCTGGGCAATGTGGTTAAACTCTGTCTCTATTCAAAATACAAAATGAG T A MRPL20 Ensembl:ENSG00000242485 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs986345098 Functional Loss SNV dbSNP153 33..33 33 - - - 12247 RMVar_ID_12247 Human_SNP_ID_313495 A-to-I Human chr1 - 1404639 1404639 1404639 AAAATTAGCTGGGCATGGTGGCCGGCACCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCTGGAGA AAAATTAGCTGGGCATGGTGGCCGGCACCTGTTGTCCCAGCTACTCAGGAGGCTGAGGCTGGAGA T A MRPL20 Ensembl:ENSG00000242485 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1485597122 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8283517,Human_RBP_ID_24580229 12248 RMVar_ID_12248 Human_SNP_ID_314107 A-to-I Human chr1 - 1406287 1406287 1406287 GGAGTGCAATGGCGCGATCTAGGCTTAATGCAACCTCGTCTCCCGGGTTCAAGCGATTTTCCCGC GGAGTGCAATGGCGCGATCTAGGCTTAATGCATCCTCGTCTCCCGGGTTCAAGCGATTTTCCCGC T A MRPL20 Ensembl:ENSG00000242485 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1405849422 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10555208 Human_Splice_Rec_4029,Human_Splice_Rec_4048 12249 RMVar_ID_12249 Human_SNP_ID_314108 A-to-I Human chr1 - 1406287 1406287 1406287 GGAGTGCAATGGCGCGATCTAGGCTTAATGCAACCTCGTCTCCCGGGTTCAAGCGATTTTCCCGC GGAGTGCAATGGCGCGATCTAGGCTTAATGCAGCCTCGTCTCCCGGGTTCAAGCGATTTTCCCGC T C MRPL20 Ensembl:ENSG00000242485 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1405849422 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10555208 Human_Splice_Rec_4029,Human_Splice_Rec_4048 12250 RMVar_ID_12250 Human_SNP_ID_314867 A-to-I Human chr1 + 1407829 1407829 1407829 GCGGCCTCTGCCTTCCTAGTAGCTGGGACGTCAGGCGCGCGCCGCCACGCCCGGCTAATTTTTTG GCGGCCTCTGCCTTCCTAGTAGCTGGGACGTCGGGCGCGCGCCGCCACGCCCGGCTAATTTTTTG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs899792494 Functional Loss SNV dbSNP153 33..33 33 - - - 12251 RMVar_ID_12251 Human_SNP_ID_314878 A-to-I Human chr1 + 1407853 1407853 1407853 GGGACGTCAGGCGCGCGCCGCCACGCCCGGCTAATTTTTTGTGTTTTTTGTAGAGGGGGCGTCTT GGGACGTCAGGCGCGCGCCGCCACGCCCGGCTTATTTTTTGTGTTTTTTGTAGAGGGGGCGTCTT A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs890960123 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24446869 12252 RMVar_ID_12252 Human_SNP_ID_315431 A-to-I Human chr1 + 1409269 1409269 1409269 CGAGACCAGCCTGGCCAACATGGTGGAACCCCATCTCTACTAAAAATGCAAAAAGTAGCCGGGCG CGAGACCAGCCTGGCCAACATGGTGGAACCCCGTCTCTACTAAAAATGCAAAAAGTAGCCGGGCG A G AL391244.2 Ensembl:ENSG00000272455 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs923266175 Functional Loss SNV dbSNP153 33..33 33 - - - 12253 RMVar_ID_12253 Human_SNP_ID_315473 A-to-I Human chr1 + 1409385 1409385 1409385 GGGAGGCCAAGGCTGCAGTGAGCCAAGATCGCACCACTGCACTCTAGCGTGGGTGACAGATCAAG GGGAGGCCAAGGCTGCAGTGAGCCAAGATCGCGCCACTGCACTCTAGCGTGGGTGACAGATCAAG A G AL391244.2 Ensembl:ENSG00000272455 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1298831224 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17556472,Human_RBP_ID_22707814 12254 RMVar_ID_12254 Human_SNP_ID_315564 A-to-I Human chr1 + 1409618 1409618 1409618 GTGCATGCCTGGCCAATTTTTGTATTTTTGGTAGAAATGGAGTTTCACCATGTTGCCCAGGCTGG GTGCATGCCTGGCCAATTTTTGTATTTTTGGTGGAAATGGAGTTTCACCATGTTGCCCAGGCTGG A G AL391244.2 Ensembl:ENSG00000272455 lincRNA exon GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs958122936 Functional Loss SNV dbSNP153 33..33 33 - - - 12255 RMVar_ID_12255 Human_SNP_ID_322613 A-to-I Human chr1 + 1428949 1428949 1428949 GTGAACCTGGGAGGCAAAGCTTGCAGTGAGCCAAGATCACGCCACTGCACTCTAGCTTGGGCGAA GTGAACCTGGGAGGCAAAGCTTGCAGTGAGCCGAGATCACGCCACTGCACTCTAGCTTGGGCGAA A G lnc-TMEM88B-1,lnc-TMEM88B-1:2 RNACentral:URS00008B796E,RNACentral:URS00009B0C87 lincRNA,lincRNA exon,exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1380310212 Functional Loss SNV dbSNP153 33..33 33 - - - 12256 RMVar_ID_12256 Human_SNP_ID_322940 A-to-I Human chr1 + 1429960 1429960 1429960 CTAGCTCTCTGCAGCCTCGCCCTCCCAGGCTCAAGTGATCCTCCTGCCTCAGCCTCCCAAGTAGC CTAGCTCTCTGCAGCCTCGCCCTCCCAGGCTCTAGTGATCCTCCTGCCTCAGCCTCCCAAGTAGC A T lnc-TMEM88B-1,lnc-TMEM88B-1:2 RNACentral:URS00008B796E,RNACentral:URS00009B0C87 lincRNA,lincRNA intron,intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs890507882 Functional Loss SNV dbSNP153 33..33 33 - - - 12257 RMVar_ID_12257 Human_SNP_ID_329957 A-to-I Human chr1 + 1450164 1450164 1450164 TCCTGGCTAACACGGTGAAACCGTCTCTACTAAAACTACAAAAATTAGCCGGGTGTGGTGGCGGT TCCTGGCTAACACGGTGAAACCGTCTCTACTACAACTACAAAAATTAGCCGGGTGTGGTGGCGGT A C ATAD3C Ensembl:ENSG00000215915 Protein coding 5'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs933258080 Functional Loss SNV dbSNP153 33..33 33 - - - 12258 RMVar_ID_12258 Human_SNP_ID_329987 A-to-I Human chr1 + 1450240 1450240 1450240 CCAGCTACTCGGGAGGCTGAGGCAGGAGAGTGACGTGAACCCGAGAGGTAGAGCTTGCAGTAAGC CCAGCTACTCGGGAGGCTGAGGCAGGAGAGTGGCGTGAACCCGAGAGGTAGAGCTTGCAGTAAGC A G ATAD3C Ensembl:ENSG00000215915 Protein coding 5'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1307943953 Functional Loss SNV dbSNP153 33..33 33 - - - 12259 RMVar_ID_12259 Human_SNP_ID_329994 A-to-I Human chr1 + 1450257 1450255 1450257 TGAGGCAGGAGAGTGACGTGAACCCGAGAGGTAGAGCTTGCAGTAAGCAGAGATCATGCCACTGC TGAGGCAGGAGAGTGACGTGAACCCGAGAGG__GAGCTTGCAGTAAGCAGAGATCATGCCACTGC GTA G ATAD3C Ensembl:ENSG00000215915 Protein coding 5'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1360714879 Functional Loss DEL dbSNP153 32..33 33 - - - 12260 RMVar_ID_12260 Human_SNP_ID_329996 A-to-I Human chr1 + 1450257 1450257 1450257 TGAGGCAGGAGAGTGACGTGAACCCGAGAGGTAGAGCTTGCAGTAAGCAGAGATCATGCCACTGC TGAGGCAGGAGAGTGACGTGAACCCGAGAGGTGGAGCTTGCAGTAAGCAGAGATCATGCCACTGC A G ATAD3C Ensembl:ENSG00000215915 Protein coding 5'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1225387551 Functional Loss SNV dbSNP153 33..33 33 - - - 12261 RMVar_ID_12261 Human_SNP_ID_329998 A-to-I Human chr1 + 1450269 1450269 1450269 GTGACGTGAACCCGAGAGGTAGAGCTTGCAGTAAGCAGAGATCATGCCACTGCACTCCAGCCTGG GTGACGTGAACCCGAGAGGTAGAGCTTGCAGTGAGCAGAGATCATGCCACTGCACTCCAGCCTGG A G ATAD3C Ensembl:ENSG00000215915 Protein coding 5'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1370603951 Functional Loss SNV dbSNP153 33..33 33 - - - 12262 RMVar_ID_12262 Human_SNP_ID_338505 A-to-I Human chr1 + 1473195 1473195 1473195 TGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCAGTGACGTGATCTCCACTCACTGCAAGCTCCGC TGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCGGTGACGTGATCTCCACTCACTGCAAGCTCCGC A G ATAD3B Ensembl:ENSG00000160072 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs548957905 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10555563 RMVar_hsa_circ_92996,RMVar_hsa_circ_128329 12263 RMVar_ID_12263 Human_SNP_ID_342639 A-to-I Human chr1 + 1483062 1483062 1483062 CAGGCCTGTAATCCCAGCATTTTCGGAGGCGGAGGTGGGCGGATCACGAGGTCCGGAGATCGAGA CAGGCCTGTAATCCCAGCATTTTCGGAGGCGGCGGTGGGCGGATCACGAGGTCCGGAGATCGAGA A C ATAD3B Ensembl:ENSG00000160072 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1469415411 Functional Loss SNV dbSNP153 33..33 33 - - - 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 12264 RMVar_ID_12264 Human_SNP_ID_342646 A-to-I Human chr1 + 1483075 1483075 1483075 CCAGCATTTTCGGAGGCGGAGGTGGGCGGATCACGAGGTCCGGAGATCGAGATCATCCTGGTAAG CCAGCATTTTCGGAGGCGGAGGTGGGCGGATCTCGAGGTCCGGAGATCGAGATCATCCTGGTAAG A T ATAD3B Ensembl:ENSG00000160072 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1557802475 Functional Loss SNV dbSNP153 33..33 33 - - - 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 12265 RMVar_ID_12265 Human_SNP_ID_342667 A-to-I Human chr1 + 1483108 1483108 1483108 CGAGGTCCGGAGATCGAGATCATCCTGGTAAGAGTGAAACCCTGTCTCTACTAAAAAAAAGAAAA CGAGGTCCGGAGATCGAGATCATCCTGGTAAGGGTGAAACCCTGTCTCTACTAAAAAAAAGAAAA A G ATAD3B Ensembl:ENSG00000160072 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs568307114 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22872497,Human_RBP_ID_24751162 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 12266 RMVar_ID_12266 Human_SNP_ID_343152 A-to-I Human chr1 + 1484251 1484251 1484251 GTGTGCTGCTCAAGTGCAGTGGCGCGATCTCGACTCACTGTCAGCTTCGCCTCTTGGGTTCACAC GTGTGCTGCTCAAGTGCAGTGGCGCGATCTCGTCTCACTGTCAGCTTCGCCTCTTGGGTTCACAC A T ATAD3B Ensembl:ENSG00000160072 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1467562962 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10556413,Human_RBP_ID_18549984 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 12267 RMVar_ID_12267 Human_SNP_ID_343205 A-to-I Human chr1 + 1484366 1484366 1484366 CCACGCCCGGCTAATTTTTTTGTATTTTTAGTAGAGAGAGGGTTTCATCCTGTTAGCCAAGATGG CCACGCCCGGCTAATTTTTTTGTATTTTTAGTGGAGAGAGGGTTTCATCCTGTTAGCCAAGATGG A G ATAD3B Ensembl:ENSG00000160072 Protein coding intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1420581817 Functional Loss SNV dbSNP153 33..33 33 - - - 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 12268 RMVar_ID_12268 Human_SNP_ID_343274 A-to-I Human chr1 + 1484568 1484567 1484568 TAGGCTGGTCTTGAACTCCAACCTCTGGTGATACGCCGGCCTTGGCCTCCCAAAGTGCTGGGATT TAGGCTGGTCTTGAACTCCAACCTCTGGTGAT_CGCCGGCCTTGGCCTCCCAAAGTGCTGGGATT TA T ATAD3B Ensembl:ENSG00000160072 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1195922304 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_17556841 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 12269 RMVar_ID_12269 Human_SNP_ID_349000 A-to-I Human chr1 + 1497755 1497755 1497755 CGGCATGGTGGTAGGTGACTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGACTCGCTTGGA CGGCATGGTGGTAGGTGACTGTAATCCCAGCTGCTCGGGAGGCTGAGGCAGGAGACTCGCTTGGA A G ATAD3B Ensembl:ENSG00000160072 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348162647 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24580569 RMVar_hsa_circ_89217,RMVar_hsa_circ_128331,RMVar_hsa_circ_85673,RMVar_hsa_circ_128342,RMVar_hsa_circ_99522,RMVar_hsa_circ_104837,RMVar_hsa_circ_128344,RMVar_hsa_circ_128346,RMVar_hsa_circ_128347 12270 RMVar_ID_12270 Human_SNP_ID_349835 A-to-I Human chr1 + 1499442 1499442 1499442 TATTTTTAGTAGAGAGGGGGTTATACCATGTTAGCCAGGATGGTCTTAAACTCCTGACCTCATGA TATTTTTAGTAGAGAGGGGGTTATACCATGTTCGCCAGGATGGTCTTAAACTCCTGACCTCATGA A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1178736444 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_104837,RMVar_hsa_circ_128344,RMVar_hsa_circ_128346,RMVar_hsa_circ_128347 12271 RMVar_ID_12271 Human_SNP_ID_350939 A-to-I Human chr1 + 1501978 1501978 1501978 TTGGCTCACCGCAACCTCCATCTCCTGGGTTCAAGCAATTCTCCTGGCTCAGCCTCCCGTGTAGC TTGGCTCACCGCAACCTCCATCTCCTGGGTTCTAGCAATTCTCCTGGCTCAGCCTCCCGTGTAGC A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1219376449 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_104837,RMVar_hsa_circ_128344,RMVar_hsa_circ_128346,RMVar_hsa_circ_128347 12272 RMVar_ID_12272 Human_SNP_ID_358429 A-to-I Human chr1 + 1521929 1521929 1521929 TTTTGTATTTTTAGTAGAGATGGGTTTTCACCATGTTGGCCAGGCTGGTCACGAACTTCTGACCT TTTTGTATTTTTAGTAGAGATGGGTTTTCACCGTGTTGGCCAGGCTGGTCACGAACTTCTGACCT A G ATAD3A Ensembl:ENSG00000197785 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs760361036 Functional Loss SNV dbSNP153 33..33 33 - - - 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 12273 RMVar_ID_12273 Human_SNP_ID_358523 A-to-I Human chr1 + 1522224 1522224 1522224 ACCATGGCCAGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCTCCATGTGGGTTAGGCTGG ACCATGGCCAGCTAATTTTTTGTATTTTTAGTGGAGACGGGGTTTCTCCATGTGGGTTAGGCTGG A G ATAD3A Ensembl:ENSG00000197785 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1352064094 Functional Loss SNV dbSNP153 33..33 33 - - - 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 12274 RMVar_ID_12274 Human_SNP_ID_361072 A-to-I Human chr1 + 1528029 1528029 1528029 TCGCCCAGGCTGGAGTGCAGTGACACGATCTCAGCTGACTGCAACCTCTGCCTCCCGGGTTCAAA TCGCCCAGGCTGGAGTGCAGTGACACGATCTCTGCTGACTGCAACCTCTGCCTCCCGGGTTCAAA A T ATAD3A Ensembl:ENSG00000197785 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1427377124 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10561365 RMVar_hsa_circ_99522,RMVar_hsa_circ_128347 12275 RMVar_ID_12275 Human_SNP_ID_371146 A-to-I Human chr1 - 1555781 1555781 1555781 GTTGCCCAGGCTGGTCTTGGATTCCTGAACTCAAGCAGTCTGCCTGCCTTGGCCTCCCAGAGTGC GTTGCCCAGGCTGGTCTTGGATTCCTGAACTCTAGCAGTCTGCCTGCCTTGGCCTCCCAGAGTGC T A SSU72 Ensembl:ENSG00000160075 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1382577762 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8284259,Human_RBP_ID_10564657 RMVar_hsa_circ_106584,RMVar_hsa_circ_84662,RMVar_hsa_circ_39982,RMVar_hsa_circ_128355,RMVar_hsa_circ_128356 12276 RMVar_ID_12276 Human_SNP_ID_371159 A-to-I Human chr1 - 1555825 1555825 1555825 CTGGCCTGATTTTTTTATTTTTAGTAGAAATGAGGTTTCGCCCTGTTGCCCAGGCTGGTCTTGGA CTGGCCTGATTTTTTTATTTTTAGTAGAAATGGGGTTTCGCCCTGTTGCCCAGGCTGGTCTTGGA T C SSU72 Ensembl:ENSG00000160075 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1301206493 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10564658 RMVar_hsa_circ_106584,RMVar_hsa_circ_84662,RMVar_hsa_circ_39982,RMVar_hsa_circ_128355,RMVar_hsa_circ_128356 12277 RMVar_ID_12277 Human_SNP_ID_371160 A-to-I Human chr1 - 1555829 1555829 1555829 CCACCTGGCCTGATTTTTTTATTTTTAGTAGAAATGAGGTTTCGCCCTGTTGCCCAGGCTGGTCT CCACCTGGCCTGATTTTTTTATTTTTAGTAGAGATGAGGTTTCGCCCTGTTGCCCAGGCTGGTCT T C SSU72 Ensembl:ENSG00000160075 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1489517302 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10564658 RMVar_hsa_circ_106584,RMVar_hsa_circ_84662,RMVar_hsa_circ_39982,RMVar_hsa_circ_128355,RMVar_hsa_circ_128356 12278 RMVar_ID_12278 Human_SNP_ID_372382 A-to-I Human chr1 - 1559906 1559906 1559906 AGCCTGACCAAAATGGAGAAACCCCCGTCTCTACTAAAAATAAAAAATTAGCCGGCCATCGTGGT AGCCTGACCAAAATGGAGAAACCCCCGTCTCTGCTAAAAATAAAAAATTAGCCGGCCATCGTGGT T C SSU72 Ensembl:ENSG00000160075 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs765706438 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106584,RMVar_hsa_circ_84662,RMVar_hsa_circ_39982,RMVar_hsa_circ_128355,RMVar_hsa_circ_128356 12279 RMVar_ID_12279 Human_SNP_ID_372423 A-to-I Human chr1 - 1560020 1560020 1560020 AAACCCTGTCTCTACTAAAAGTACAAAACGCTAGGCATGGTGGCACATGCCTGTAATCCCAGCAC AAACCCTGTCTCTACTAAAAGTACAAAACGCTTGGCATGGTGGCACATGCCTGTAATCCCAGCAC T A SSU72 Ensembl:ENSG00000160075 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1296593370 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106584,RMVar_hsa_circ_84662,RMVar_hsa_circ_39982,RMVar_hsa_circ_128355,RMVar_hsa_circ_128356 12280 RMVar_ID_12280 Human_SNP_ID_372424 A-to-I Human chr1 - 1560020 1560020 1560020 AAACCCTGTCTCTACTAAAAGTACAAAACGCTAGGCATGGTGGCACATGCCTGTAATCCCAGCAC AAACCCTGTCTCTACTAAAAGTACAAAACGCTCGGCATGGTGGCACATGCCTGTAATCCCAGCAC T G SSU72 Ensembl:ENSG00000160075 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1296593370 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106584,RMVar_hsa_circ_84662,RMVar_hsa_circ_39982,RMVar_hsa_circ_128355,RMVar_hsa_circ_128356 12281 RMVar_ID_12281 Human_SNP_ID_372514 A-to-I Human chr1 - 1560288 1560288 1560288 CACACAGATGTGGTGGGTGTGGTGGCACAGCTACTCGGGAAGCTGAGGCAGGAGGCTTCACTGAG CACACAGATGTGGTGGGTGTGGTGGCACAGCTTCTCGGGAAGCTGAGGCAGGAGGCTTCACTGAG T A SSU72 Ensembl:ENSG00000160075 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1210561714 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5685079,Human_RBP_ID_22779723 RMVar_hsa_circ_106584,RMVar_hsa_circ_84662,RMVar_hsa_circ_39982,RMVar_hsa_circ_128355,RMVar_hsa_circ_128356 12282 RMVar_ID_12282 Human_SNP_ID_372880 A-to-I Human chr1 - 1561364 1561364 1561364 TCAAGACAAAGGACGGGCCGGCGCGGTGACTCAGGCCTGTAATCCCAGCACTTTGGGAGGCCGAG TCAAGACAAAGGACGGGCCGGCGCGGTGACTCGGGCCTGTAATCCCAGCACTTTGGGAGGCCGAG T C SSU72 Ensembl:ENSG00000160075 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs974988033 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10565038 RMVar_hsa_circ_106584,RMVar_hsa_circ_84662,RMVar_hsa_circ_39982,RMVar_hsa_circ_128355,RMVar_hsa_circ_128356,RMVar_hsa_circ_128357 12283 RMVar_ID_12283 Human_SNP_ID_373533 A-to-I Human chr1 - 1563277 1563277 1563277 CAGCTGCCTCGGCCTCTCAGAGTGTTGGGATTACAGGCGTGAGCCACCATGCCTGGCCTCTTGGA CAGCTGCCTCGGCCTCTCAGAGTGTTGGGATTGCAGGCGTGAGCCACCATGCCTGGCCTCTTGGA T C SSU72 Ensembl:ENSG00000160075 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs565242985 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10565432,Human_RBP_ID_24583224 RMVar_hsa_circ_106584,RMVar_hsa_circ_84662,RMVar_hsa_circ_39982,RMVar_hsa_circ_128355,RMVar_hsa_circ_128356,RMVar_hsa_circ_87449,RMVar_hsa_circ_108941,RMVar_hsa_circ_128357,RMVar_hsa_circ_128358,RMVar_hsa_circ_128359 12284 RMVar_ID_12284 Human_SNP_ID_373586 A-to-I Human chr1 - 1563455 1563452 1563455 TGATCTCAGCTCACTGCAACCTCCCCCTCCCAAGTTCAAGCGATTCTCTGCCTCAGCCTCCCGAA TGATCTCAGCTCACTGCAACCTCCCCCTCCCA___TCAAGCGATTCTCTGCCTCAGCCTCCCGAA AACT A SSU72 Ensembl:ENSG00000160075 Protein coding intron GSE38233;GSE107867 cultured B-cells;ASD brains,frontal_cortex - 24183664,30559470 RNA-Seq:(High) rs1477167597 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_5244998,Human_RBP_ID_9553177,Human_RBP_ID_10565450,Human_RBP_ID_24583247 RMVar_hsa_circ_106584,RMVar_hsa_circ_84662,RMVar_hsa_circ_39982,RMVar_hsa_circ_128355,RMVar_hsa_circ_128356,RMVar_hsa_circ_87449,RMVar_hsa_circ_108941,RMVar_hsa_circ_128357,RMVar_hsa_circ_128358,RMVar_hsa_circ_128359 12285 RMVar_ID_12285 Human_SNP_ID_373596 A-to-I Human chr1 - 1563480 1563480 1563480 TTGCCCAAGGTGGAGTGTAGCGGCTTGATCTCAGCTCACTGCAACCTCCCCCTCCCAAGTTCAAG TTGCCCAAGGTGGAGTGTAGCGGCTTGATCTCGGCTCACTGCAACCTCCCCCTCCCAAGTTCAAG T C SSU72 Ensembl:ENSG00000160075 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1383264145 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5244998,Human_RBP_ID_5685355,Human_RBP_ID_8241257,Human_RBP_ID_10565451,Human_RBP_ID_18509775 RMVar_hsa_circ_106584,RMVar_hsa_circ_84662,RMVar_hsa_circ_39982,RMVar_hsa_circ_128355,RMVar_hsa_circ_128356,RMVar_hsa_circ_87449,RMVar_hsa_circ_108941,RMVar_hsa_circ_128357,RMVar_hsa_circ_128358,RMVar_hsa_circ_128359 12286 RMVar_ID_12286 Human_SNP_ID_376170 A-to-I Human chr1 - 1571123 1571123 1571123 CTCCTGCCTCAGCCTCCTGAGTAACTGGGACTACAGGCACCCGCTACCACGCCCGGCTAATTTTT CTCCTGCCTCAGCCTCCTGAGTAACTGGGACTGCAGGCACCCGCTACCACGCCCGGCTAATTTTT T C SSU72 Ensembl:ENSG00000160075 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs970787215 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84662,RMVar_hsa_circ_128356,RMVar_hsa_circ_108941,RMVar_hsa_circ_128359 12287 RMVar_ID_12287 Human_SNP_ID_386728 A-to-I Human chr1 - 1598914 1598914 1598914 TGTGCTTTGCAGGCCTGGGGCGCAGCTCTCCAAGCCTGTCCTGCCCCGCCCCACCCCACTGGGCT TGTGCTTTGCAGGCCTGGGGCGCAGCTCTCCAGGCCTGTCCTGCCCCGCCCCACCCCACTGGGCT T C FNDC10 Ensembl:ENSG00000228594 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1266587671 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_326711 12288 RMVar_ID_12288 Human_SNP_ID_389887 A-to-I Human chr1 + 1607371 1607369 1607371 TCCTTTTTTTTTTTTTTTTTTTTGAGAGTCTCACTCTGTTGCCTAGACTGGAGTGCAATGGCGTG TCCTTTTTTTTTTTTTTTTTTTTGAGAGTCT__CTCTGTTGCCTAGACTGGAGTGCAATGGCGTG TCA T LOC105378586 RNACentral:URS00008BC95F lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1340655476 Functional Loss DEL dbSNP153 32..33 33 - - - 12289 RMVar_ID_12289 Human_SNP_ID_402249 A-to-I Human chr1 - 1638883 1638883 1638883 TTGGCCGGGCTGGTCTTGAACTCCTGGGCTCAAGCAGTCCTCCTGCCTTGCCCTCCCAAAGTGCT TTGGCCGGGCTGGTCTTGAACTCCTGGGCTCAGGCAGTCCTCCTGCCTTGCCCTCCCAAAGTGCT T C CDK11B Ensembl:ENSG00000248333 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1434341445 Functional Loss SNV dbSNP153 33..33 33 - - - 12290 RMVar_ID_12290 Human_SNP_ID_411252 A-to-I Human chr1 - 1663639 1663639 1663639 TGATGAAACCCTGTCTCTACCAAAAATACAAAAATTAGCTGGGTGCGATGGTGGGTGCCTGTAAT TGATGAAACCCTGTCTCTACCAAAAATACAAACATTAGCTGGGTGCGATGGTGGGTGCCTGTAAT T G SLC35E2B Ensembl:ENSG00000189339 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs186992805 Functional Loss SNV dbSNP153 33..33 33 - - - 12291 RMVar_ID_12291 Human_SNP_ID_411389 A-to-I Human chr1 - 1664075 1664075 1664075 GGGCTCAAATGATCCTCCCACCTCAGCCTCCCATGTGGCTGGAACCACAGGCACGTGCCACCATG GGGCTCAAATGATCCTCCCACCTCAGCCTCCCTTGTGGCTGGAACCACAGGCACGTGCCACCATG T A SLC35E2B Ensembl:ENSG00000189339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1480565089 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26387147 12292 RMVar_ID_12292 Human_SNP_ID_411404 A-to-I Human chr1 - 1664101 1664101 1664101 TTGGCTCACTGCAGCCTCGACTTCCTGGGCTCAAATGATCCTCCCACCTCAGCCTCCCATGTGGC TTGGCTCACTGCAGCCTCGACTTCCTGGGCTCCAATGATCCTCCCACCTCAGCCTCCCATGTGGC T G SLC35E2B Ensembl:ENSG00000189339 Protein coding intron GSE47997;GSE38233;GSE100210;GSE99789;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BERP35T1 cell line - 23474544,24183664,29129909,29796672,31158229 RNA-Seq:(High) rs1461739814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26387147,Human_RBP_ID_27169947 12293 RMVar_ID_12293 Human_SNP_ID_411418 A-to-I Human chr1 - 1664147 1664142 1664147 AGTCTTGCTCTGTCTGTCACCCAGGCTGGAGTACAGTGGCATGATCTTGGCTCACTGCAGCCTCG AGTCTTGCTCTGTCTGTCACCCAGGCTGGAGT_____GGCATGATCTTGGCTCACTGCAGCCTCG CACTGT C SLC35E2B Ensembl:ENSG00000189339 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,31158229,31158229,31158229 RNA-Seq:(High) rs1298679888 Functional Loss DEL dbSNP153 33..37 33 - - - 12294 RMVar_ID_12294 Human_SNP_ID_411420 A-to-I Human chr1 - 1664145 1664145 1664145 TCTTGCTCTGTCTGTCACCCAGGCTGGAGTACAGTGGCATGATCTTGGCTCACTGCAGCCTCGAC TCTTGCTCTGTCTGTCACCCAGGCTGGAGTACGGTGGCATGATCTTGGCTCACTGCAGCCTCGAC T C SLC35E2B Ensembl:ENSG00000189339 Protein coding intron GSE38233;GSE107867 cultured B-cells;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 24183664,30559470 RNA-Seq:(High) rs1441300381 Functional Loss SNV dbSNP153 33..33 33 - - - 12295 RMVar_ID_12295 Human_SNP_ID_411422 A-to-I Human chr1 - 1664147 1664147 1664147 AGTCTTGCTCTGTCTGTCACCCAGGCTGGAGTACAGTGGCATGATCTTGGCTCACTGCAGCCTCG AGTCTTGCTCTGTCTGTCACCCAGGCTGGAGTGCAGTGGCATGATCTTGGCTCACTGCAGCCTCG T C SLC35E2B Ensembl:ENSG00000189339 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,31158229,31158229,31158229 RNA-Seq:(High) rs1188111867 Functional Loss SNV dbSNP153 33..33 33 - - - 12296 RMVar_ID_12296 Human_SNP_ID_412256 A-to-I Human chr1 - 1666716 1666672 1666716 CACGCCCAGCCTCCCACAGTGCTGGGGTTACAAGCATGAGCCCCCACACCCAGCCTCCCACAGTG CACGCCCAGCCTCCCACAGTGCTGGGGTTACAA_________________________________ CTGTAACCCCAGCACTGTGGGAGGCTGGGTGTGGGGGCTCATGCT C SLC35E2B Ensembl:ENSG00000189339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1474675297 Functional Loss DEL dbSNP153 33..65 33 - - - 12297 RMVar_ID_12297 Human_SNP_ID_412277 A-to-I Human chr1 - 1666716 1666716 1666716 CACGCCCAGCCTCCCACAGTGCTGGGGTTACAAGCATGAGCCCCCACACCCAGCCTCCCACAGTG CACGCCCAGCCTCCCACAGTGCTGGGGTTACAGGCATGAGCCCCCACACCCAGCCTCCCACAGTG T C SLC35E2B Ensembl:ENSG00000189339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1255042654 Functional Loss SNV dbSNP153 33..33 33 - - - 12298 RMVar_ID_12298 Human_SNP_ID_412278 A-to-I Human chr1 - 1666716 1666716 1666716 CACGCCCAGCCTCCCACAGTGCTGGGGTTACAAGCATGAGCCCCCACACCCAGCCTCCCACAGTG CACGCCCAGCCTCCCACAGTGCTGGGGTTACACGCATGAGCCCCCACACCCAGCCTCCCACAGTG T G SLC35E2B Ensembl:ENSG00000189339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1255042654 Functional Loss SNV dbSNP153 33..33 33 - - - 12299 RMVar_ID_12299 Human_SNP_ID_415848 A-to-I Human chr1 - 1677513 1677513 1677513 AGATCACGCCTCTGCACTTCAGCCTGGGCGACAGAGCAATACTCCGTCTCAAAAAAAAAAAAAAA AGATCACGCCTCTGCACTTCAGCCTGGGCGACGGAGCAATACTCCGTCTCAAAAAAAAAAAAAAA T C SLC35E2B Ensembl:ENSG00000189339 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1283668866 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109097,RMVar_hsa_circ_373013,RMVar_hsa_circ_128365,RMVar_hsa_circ_128367,RMVar_hsa_circ_108822,RMVar_hsa_circ_128370 12300 RMVar_ID_12300 Human_SNP_ID_415923 A-to-I Human chr1 - 1677691 1677691 1677691 ACGAGGTCAGGAGATCGAGACCATCCTGGCTAACACGGTGAAAACCCGTCTCTACTAAAAAAAAA ACGAGGTCAGGAGATCGAGACCATCCTGGCTAGCACGGTGAAAACCCGTCTCTACTAAAAAAAAA T C SLC35E2B Ensembl:ENSG00000189339 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1198271540 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2709452,Human_miRNA_ID_2709453 RMVar_hsa_circ_109097,RMVar_hsa_circ_373013,RMVar_hsa_circ_128365,RMVar_hsa_circ_128367,RMVar_hsa_circ_108822,RMVar_hsa_circ_128370 12301 RMVar_ID_12301 Human_SNP_ID_416915 A-to-I Human chr1 - 1680185 1680185 1680185 GCAATCCTCCCACCCCAGCCTCCTAAGTAGTTAGGACTACAGACATGCACCACCATGCCCGGCTA GCAATCCTCCCACCCCAGCCTCCTAAGTAGTTTGGACTACAGACATGCACCACCATGCCCGGCTA T A SLC35E2B Ensembl:ENSG00000189339 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1371947216 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109097,RMVar_hsa_circ_373013,RMVar_hsa_circ_128365,RMVar_hsa_circ_128367,RMVar_hsa_circ_108822,RMVar_hsa_circ_128370 12302 RMVar_ID_12302 Human_SNP_ID_419342 A-to-I Human chr1 - 1687787 1687787 1687787 GGGTTCAAGCGATTCTCATGCCTCAGCCTCCTAAGTGGCTGGGACTACAGGCACCCGCCAGGATT GGGTTCAAGCGATTCTCATGCCTCAGCCTCCTGAGTGGCTGGGACTACAGGCACCCGCCAGGATT T C SLC35E2B Ensembl:ENSG00000189339 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1485493656 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109097,RMVar_hsa_circ_373013,RMVar_hsa_circ_128365,RMVar_hsa_circ_128367,RMVar_hsa_circ_108822,RMVar_hsa_circ_128370 12303 RMVar_ID_12303 Human_SNP_ID_419815 A-to-I Human chr1 - 1689050 1689050 1689050 CTCGTGCCTCAGCCTCCTGTGTAGTTGGGACTACTGGCACCCACCACCACGTCCAGCTAAGTTTT CTCGTGCCTCAGCCTCCTGTGTAGTTGGGACTGCTGGCACCCACCACCACGTCCAGCTAAGTTTT T C SLC35E2B Ensembl:ENSG00000189339 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355142456 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10622791 RMVar_hsa_circ_109097,RMVar_hsa_circ_373013,RMVar_hsa_circ_128365,RMVar_hsa_circ_128367,RMVar_hsa_circ_108822,RMVar_hsa_circ_128370 12304 RMVar_ID_12304 Human_SNP_ID_419837 A-to-I Human chr1 - 1689125 1689125 1689125 CTCTGTCAGCCAGGTTGGAGTGTAGTGGTGCAATCTCAGCTCACTAAAGCCTCCGTCTCCCAGGT CTCTGTCAGCCAGGTTGGAGTGTAGTGGTGCAGTCTCAGCTCACTAAAGCCTCCGTCTCCCAGGT T C SLC35E2B Ensembl:ENSG00000189339 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1557768148 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1345169,Human_RBP_ID_10622846 RMVar_hsa_circ_109097,RMVar_hsa_circ_373013,RMVar_hsa_circ_128365,RMVar_hsa_circ_128367,RMVar_hsa_circ_108822,RMVar_hsa_circ_128370 12305 RMVar_ID_12305 Human_SNP_ID_421504 A-to-I Human chr1 + 1694030 1694030 1694030 ACTTTTGGCCGGGCGAGGTGGCTCACGTCTGTAATCCCAGCATTTTGAGAGGCTGAGGCGGGCGG ACTTTTGGCCGGGCGAGGTGGCTCACGTCTGTGATCCCAGCATTTTGAGAGGCTGAGGCGGGCGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1452717600 Functional Loss SNV dbSNP153 33..33 33 - - - 12306 RMVar_ID_12306 Human_SNP_ID_432385 A-to-I Human chr1 - 1726453 1726453 1726453 CCAAGGCAGGCAGATCACGAGGTCACGAGATCAAGACCATCCTGGCTAACACAGTGAAACCCGGT CCAAGGCAGGCAGATCACGAGGTCACGAGATCGAGACCATCCTGGCTAACACAGTGAAACCCGGT T C SLC35E2A,AL031282.2 Ensembl:ENSG00000215790,Ensembl:ENSG00000268575 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1368412158 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128367,RMVar_hsa_circ_108822 12307 RMVar_ID_12307 Human_SNP_ID_433250 A-to-I Human chr1 - 1729416 1729414 1729416 AGATCGTGCCATTGCACTCCAGCCTGGGCAACAGGGCAAGATTCCGTCTCAAAAACAAACACTAT AGATCGTGCCATTGCACTCCAGCCTGGGCAAC__GGCAAGATTCCGTCTCAAAAACAAACACTAT CCT C SLC35E2A,AL031282.2 Ensembl:ENSG00000215790,Ensembl:ENSG00000268575 Protein coding,lincRNA intron,intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-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 12308 RMVar_ID_12308 Human_SNP_ID_433271 A-to-I Human chr1 - 1729505 1729505 1729505 GTGATGGTGGGTGCCTGTAATCTCAGCTACTCAGGAGGCTGAGGCAGGAGAATTGTTTGAACCCC GTGATGGTGGGTGCCTGTAATCTCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGTTTGAACCCC T C SLC35E2A,AL031282.2 Ensembl:ENSG00000215790,Ensembl:ENSG00000268575 Protein coding,lincRNA intron,intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs975541340 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128367,RMVar_hsa_circ_108822,RMVar_hsa_circ_116436,RMVar_hsa_circ_128373 12309 RMVar_ID_12309 Human_SNP_ID_433292 A-to-I Human chr1 - 1729594 1729594 1729594 ATGGCGGATCACAAGGCCAGGAGTTCGAGACCAGCCTGGCCAACATGATGAAACCCTGTCTCTAC ATGGCGGATCACAAGGCCAGGAGTTCGAGACCGGCCTGGCCAACATGATGAAACCCTGTCTCTAC T C SLC35E2A,AL031282.2 Ensembl:ENSG00000215790,Ensembl:ENSG00000268575 Protein coding,lincRNA intron,intron GSE123020:GSM3490829,GSM3490830,GSM3490831 esophageal squamous carcinoma cells,EC109 cell line - 32596459 RNA-Seq:(High) rs1186939996 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128367,RMVar_hsa_circ_108822,RMVar_hsa_circ_116436,RMVar_hsa_circ_128373 12310 RMVar_ID_12310 Human_SNP_ID_433298 A-to-I Human chr1 - 1729616 1729616 1729616 CCAGCACTTTGGGAGGCTGCAGATGGCGGATCACAAGGCCAGGAGTTCGAGACCAGCCTGGCCAA CCAGCACTTTGGGAGGCTGCAGATGGCGGATCCCAAGGCCAGGAGTTCGAGACCAGCCTGGCCAA T G SLC35E2A,AL031282.2 Ensembl:ENSG00000215790,Ensembl:ENSG00000268575 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1308012370 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3333960 RMVar_hsa_circ_128367,RMVar_hsa_circ_108822,RMVar_hsa_circ_116436,RMVar_hsa_circ_128373 12311 RMVar_ID_12311 Human_SNP_ID_433321 A-to-I Human chr1 - 1729665 1729665 1729665 TCCTCAAAAACTAATAGAAGACCGGCTGCGGTAGCTCAGGCCTCTAATCCCAGCACTTTGGGAGG TCCTCAAAAACTAATAGAAGACCGGCTGCGGTGGCTCAGGCCTCTAATCCCAGCACTTTGGGAGG T C SLC35E2A,AL031282.2 Ensembl:ENSG00000215790,Ensembl:ENSG00000268575 Protein coding,lincRNA intron,intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs796569923 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3333960,Human_RBP_ID_5642696 RMVar_hsa_circ_128367,RMVar_hsa_circ_108822,RMVar_hsa_circ_116436,RMVar_hsa_circ_128373 12312 RMVar_ID_12312 Human_SNP_ID_433834 A-to-I Human chr1 - 1731379 1731379 1731379 GGGAGATGTTCTTGTTTTTTTTTTTTTTTTTGAGACAGAGTCTCGCTCTGTCACCCAAACTGGAG GGGAGATGTTCTTGTTTTTTTTTTTTTTTTTGTGACAGAGTCTCGCTCTGTCACCCAAACTGGAG T A SLC35E2A,AL031282.2 Ensembl:ENSG00000215790,Ensembl:ENSG00000268575 Protein coding,lincRNA intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1319212593 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128367,RMVar_hsa_circ_108822,RMVar_hsa_circ_116436,RMVar_hsa_circ_128373 12313 RMVar_ID_12313 Human_SNP_ID_434113 A-to-I Human chr1 - 1732195 1732195 1732195 CTCTGTGACCCAGGCTGGAGTGTGGTGGTGCCATCTCAGCTCACTGCAACCTCCGCCTCCCTGCT CTCTGTGACCCAGGCTGGAGTGTGGTGGTGCCGTCTCAGCTCACTGCAACCTCCGCCTCCCTGCT T C SLC35E2A,AL031282.2 Ensembl:ENSG00000215790,Ensembl:ENSG00000268575 Protein coding,lincRNA intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1465233602 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5245547,Human_RBP_ID_10635814 RMVar_hsa_circ_128367,RMVar_hsa_circ_108822,RMVar_hsa_circ_116436,RMVar_hsa_circ_128373 12314 RMVar_ID_12314 Human_SNP_ID_434443 A-to-I Human chr1 - 1733003 1733003 1733003 GTCCCAGCTGCGTGGGAGGCTGAGGCATCAGAATCACTTCAGCCCGGGAGGCGGGTGTTGCAGTG GTCCCAGCTGCGTGGGAGGCTGAGGCATCAGAGTCACTTCAGCCCGGGAGGCGGGTGTTGCAGTG T C SLC35E2A,AL031282.2 Ensembl:ENSG00000215790,Ensembl:ENSG00000268575 Protein coding,lincRNA intron,intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1227604468 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128367,RMVar_hsa_circ_108822,RMVar_hsa_circ_116436,RMVar_hsa_circ_128373 12315 RMVar_ID_12315 Human_SNP_ID_434467 A-to-I Human chr1 - 1733124 1733122 1733124 TGGAGGTCAAGGCAGGCAGATTGCCTGATCTCAGGGGTTCGAGACCACCCTGGGCAACATGGGCA TGGAGGTCAAGGCAGGCAGATTGCCTGATCTC__GGGTTCGAGACCACCCTGGGCAACATGGGCA CCT C SLC35E2A,AL031282.2 Ensembl:ENSG00000215790,Ensembl:ENSG00000268575 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1286593725 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_128367,RMVar_hsa_circ_108822,RMVar_hsa_circ_116436,RMVar_hsa_circ_128373 12316 RMVar_ID_12316 Human_SNP_ID_434559 A-to-I Human chr1 - 1733421 1733421 1733421 AGAGCTGGATTTCTTTGGTTTGATCTCGGCTCACTGCAACCTCCGCCTCCCGGGTTGAAGTGATT AGAGCTGGATTTCTTTGGTTTGATCTCGGCTCCCTGCAACCTCCGCCTCCCGGGTTGAAGTGATT T G SLC35E2A,AL031282.2 Ensembl:ENSG00000215790,Ensembl:ENSG00000268575 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1216447607 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128367,RMVar_hsa_circ_108822,RMVar_hsa_circ_116436,RMVar_hsa_circ_128373 12317 RMVar_ID_12317 Human_SNP_ID_437614 A-to-I Human chr1 - 1742319 1742319 1742319 GCGATCCTCGTGCCTCAGCCTCCTGTGTACTTAGGACTACTGGCACCCACCACCATGTCCAGCTA GCGATCCTCGTGCCTCAGCCTCCTGTGTACTTGGGACTACTGGCACCCACCACCATGTCCAGCTA T C SLC35E2A Ensembl:ENSG00000215790 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1240400949 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10639557 RMVar_hsa_circ_301098,RMVar_hsa_circ_93522,RMVar_hsa_circ_128375,RMVar_hsa_circ_128376,RMVar_hsa_circ_110391,RMVar_hsa_circ_128378 12318 RMVar_ID_12318 Human_SNP_ID_447299 A-to-I Human chr1 - 1772555 1772555 1772555 GACACAGAACTGGTCTTGAACTCCTGGACTCAAGCGATCCTCCCGCCTCGGCCTCCCAAAGTGCT GACACAGAACTGGTCTTGAACTCCTGGACTCAGGCGATCCTCCCGCCTCGGCCTCCCAAAGTGCT T C NADK Ensembl:ENSG00000008130 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1412677640 Functional Loss SNV dbSNP153 33..33 33 - - - 12319 RMVar_ID_12319 Human_SNP_ID_451489 A-to-I Human chr1 - 1787079 1787079 1787079 CGTCTGCACTTAGATTCTCTGCCTCTTTTCACATTTCTTTAAACTCTGTTTAAAACAGCATGTGG CGTCTGCACTTAGATTCTCTGCCTCTTTTCACGTTTCTTTAAACTCTGTTTAAAACAGCATGTGG T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs571777560 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1345464,Human_RBP_ID_3286762,Human_RBP_ID_5713478,Human_RBP_ID_17213841,Human_RBP_ID_17331515,Human_RBP_ID_17447632,Human_RBP_ID_17731026 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 12320 RMVar_ID_12320 Human_SNP_ID_451722 A-to-I Human chr1 - 1787945 1787945 1787945 GGCTCACTGCAAGCTCCACCTCCTGGGTTCCAATGATTCTCCTACCCTAGCCTCCTGAGTAGCTG GGCTCACTGCAAGCTCCACCTCCTGGGTTCCAGTGATTCTCCTACCCTAGCCTCCTGAGTAGCTG T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946134642 Functional Loss SNV dbSNP153 33..33 33 - - - 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_128396 12321 RMVar_ID_12321 Human_SNP_ID_452938 A-to-I Human chr1 - 1792575 1792575 1792575 TCCCCTCTCAGCCTCCCGAGTAGCTGGGAACTACAGGTGTGCGCCACCACACCCAGCTAATTTTT TCCCCTCTCAGCCTCCCGAGTAGCTGGGAACTGCAGGTGTGCGCCACCACACCCAGCTAATTTTT T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs184840483 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128407,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_311382,RMVar_hsa_circ_376322,RMVar_hsa_circ_376755,RMVar_hsa_circ_369314,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_320759,RMVar_hsa_circ_89721,RMVar_hsa_circ_128403,RMVar_hsa_circ_128405,RMVar_hsa_circ_3112,RMVar_hsa_circ_128404,RMVar_hsa_circ_128402,RMVar_hsa_circ_100327,RMVar_hsa_circ_373327,RMVar_hsa_circ_375577,RMVar_hsa_circ_324378,RMVar_hsa_circ_270627,RMVar_hsa_circ_128409,RMVar_hsa_circ_128408,RMVar_hsa_circ_128406 12322 RMVar_ID_12322 Human_SNP_ID_452966 A-to-I Human chr1 - 1792667 1792667 1792667 TTTGAGATAGAGTCTCTCTCTGTCTCCAGGCTAGAGTGGAGTGGCGTGATCTCGGCTCATTGCAA TTTGAGATAGAGTCTCTCTCTGTCTCCAGGCTCGAGTGGAGTGGCGTGATCTCGGCTCATTGCAA T G GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs979059453 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128407,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_311382,RMVar_hsa_circ_376322,RMVar_hsa_circ_376755,RMVar_hsa_circ_369314,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_320759,RMVar_hsa_circ_89721,RMVar_hsa_circ_128403,RMVar_hsa_circ_128405,RMVar_hsa_circ_3112,RMVar_hsa_circ_128404,RMVar_hsa_circ_128402,RMVar_hsa_circ_100327,RMVar_hsa_circ_373327,RMVar_hsa_circ_375577,RMVar_hsa_circ_324378,RMVar_hsa_circ_270627,RMVar_hsa_circ_128409,RMVar_hsa_circ_128408,RMVar_hsa_circ_128406 12323 RMVar_ID_12323 Human_SNP_ID_453747 A-to-I Human chr1 - 1795751 1795751 1795751 AGACCTATGAGGTCATGTTTTTTGTTTTTTTGAGGCAGAGTCTCACTCTGTTGCCCAGGCTGGAG AGACCTATGAGGTCATGTTTTTTGTTTTTTTGTGGCAGAGTCTCACTCTGTTGCCCAGGCTGGAG T A GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs199628682 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128407,RMVar_hsa_circ_41253,RMVar_hsa_circ_92329,RMVar_hsa_circ_122805,RMVar_hsa_circ_127530,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_128389,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_109841,RMVar_hsa_circ_306773,RMVar_hsa_circ_342234,RMVar_hsa_circ_89721,RMVar_hsa_circ_128403,RMVar_hsa_circ_128405,RMVar_hsa_circ_3112,RMVar_hsa_circ_128404,RMVar_hsa_circ_128402,RMVar_hsa_circ_100327,RMVar_hsa_circ_373327,RMVar_hsa_circ_375577,RMVar_hsa_circ_324378,RMVar_hsa_circ_128408,RMVar_hsa_circ_128412,RMVar_hsa_circ_281145,RMVar_hsa_circ_317907,RMVar_hsa_circ_128406,RMVar_hsa_circ_376927,RMVar_hsa_circ_285895,RMVar_hsa_circ_128414,RMVar_hsa_circ_278200,RMVar_hsa_circ_128413,RMVar_hsa_circ_128411 12324 RMVar_ID_12324 Human_SNP_ID_454238 A-to-I Human chr1 - 1797718 1797718 1797718 AATTTTGGAAAGGGGGCTGGGCGCGGTGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCTGAG AATTTTGGAAAGGGGGCTGGGCGCGGTGGCTCGTGCCTATAATCCCAGCACTTTGGGAGGCTGAG T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs905452912 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128407,RMVar_hsa_circ_41253,RMVar_hsa_circ_92329,RMVar_hsa_circ_122805,RMVar_hsa_circ_127530,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_128389,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_109841,RMVar_hsa_circ_306773,RMVar_hsa_circ_342234,RMVar_hsa_circ_89721,RMVar_hsa_circ_128403,RMVar_hsa_circ_128405,RMVar_hsa_circ_3112,RMVar_hsa_circ_128404,RMVar_hsa_circ_128402,RMVar_hsa_circ_100327,RMVar_hsa_circ_373327,RMVar_hsa_circ_375577,RMVar_hsa_circ_324378,RMVar_hsa_circ_128408,RMVar_hsa_circ_128412,RMVar_hsa_circ_281145,RMVar_hsa_circ_317907,RMVar_hsa_circ_128406,RMVar_hsa_circ_376927,RMVar_hsa_circ_285895,RMVar_hsa_circ_128414,RMVar_hsa_circ_278200,RMVar_hsa_circ_128413,RMVar_hsa_circ_128411 12325 RMVar_ID_12325 Human_SNP_ID_455789 A-to-I Human chr1 - 1803797 1803797 1803797 TTGTATTTTTAGTAGAGGCGGGGTTTTGCTGTATTGGCCAGGCTGGTCTTGAACTCCTGACATTG TTGTATTTTTAGTAGAGGCGGGGTTTTGCTGTGTTGGCCAGGCTGGTCTTGAACTCCTGACATTG T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1429215737 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128407,RMVar_hsa_circ_41253,RMVar_hsa_circ_92329,RMVar_hsa_circ_122805,RMVar_hsa_circ_127530,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_128389,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_109841,RMVar_hsa_circ_306773,RMVar_hsa_circ_342234,RMVar_hsa_circ_89721,RMVar_hsa_circ_128403,RMVar_hsa_circ_128405,RMVar_hsa_circ_3112,RMVar_hsa_circ_128404,RMVar_hsa_circ_128402,RMVar_hsa_circ_100327,RMVar_hsa_circ_373327,RMVar_hsa_circ_375577,RMVar_hsa_circ_324378,RMVar_hsa_circ_128408,RMVar_hsa_circ_128412,RMVar_hsa_circ_281145,RMVar_hsa_circ_317907,RMVar_hsa_circ_128406,RMVar_hsa_circ_376927,RMVar_hsa_circ_285895,RMVar_hsa_circ_128414,RMVar_hsa_circ_278200,RMVar_hsa_circ_128413,RMVar_hsa_circ_128411 12326 RMVar_ID_12326 Human_SNP_ID_456273 A-to-I Human chr1 - 1805208 1805208 1805208 GTGATCCACCCGCCTTAGCCTCCCAAAGTGCTAGGATTACAGGCATGAGCCACCGCACCCGGCCT GTGATCCACCCGCCTTAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCACCCGGCCT T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs555377483 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128407,RMVar_hsa_circ_41253,RMVar_hsa_circ_92329,RMVar_hsa_circ_122805,RMVar_hsa_circ_127530,RMVar_hsa_circ_96576,RMVar_hsa_circ_128390,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_89721,RMVar_hsa_circ_128403,RMVar_hsa_circ_128405,RMVar_hsa_circ_3112,RMVar_hsa_circ_128404,RMVar_hsa_circ_100327,RMVar_hsa_circ_375577,RMVar_hsa_circ_324378,RMVar_hsa_circ_128416,RMVar_hsa_circ_83173,RMVar_hsa_circ_128412,RMVar_hsa_circ_281145,RMVar_hsa_circ_317907,RMVar_hsa_circ_128406,RMVar_hsa_circ_376927,RMVar_hsa_circ_285895,RMVar_hsa_circ_128414,RMVar_hsa_circ_278200,RMVar_hsa_circ_128413,RMVar_hsa_circ_271954,RMVar_hsa_circ_276555,RMVar_hsa_circ_128411,RMVar_hsa_circ_300397,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_128422,RMVar_hsa_circ_128415 12327 RMVar_ID_12327 Human_SNP_ID_456447 A-to-I Human chr1 - 1805788 1805788 1805788 CCTGTAATTCCAGCATTTTGGGAGGCTGAAGCAGGTGGATCACCTGAGGTCAGGAGTTTGAGACC CCTGTAATTCCAGCATTTTGGGAGGCTGAAGCGGGTGGATCACCTGAGGTCAGGAGTTTGAGACC T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1215519311 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128407,RMVar_hsa_circ_41253,RMVar_hsa_circ_92329,RMVar_hsa_circ_122805,RMVar_hsa_circ_127530,RMVar_hsa_circ_96576,RMVar_hsa_circ_128390,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_89721,RMVar_hsa_circ_128403,RMVar_hsa_circ_128405,RMVar_hsa_circ_3112,RMVar_hsa_circ_128404,RMVar_hsa_circ_100327,RMVar_hsa_circ_375577,RMVar_hsa_circ_324378,RMVar_hsa_circ_128416,RMVar_hsa_circ_83173,RMVar_hsa_circ_128412,RMVar_hsa_circ_281145,RMVar_hsa_circ_317907,RMVar_hsa_circ_128406,RMVar_hsa_circ_376927,RMVar_hsa_circ_285895,RMVar_hsa_circ_128414,RMVar_hsa_circ_278200,RMVar_hsa_circ_128413,RMVar_hsa_circ_271954,RMVar_hsa_circ_276555,RMVar_hsa_circ_128411,RMVar_hsa_circ_300397,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_128422,RMVar_hsa_circ_128415 12328 RMVar_ID_12328 Human_SNP_ID_456707 A-to-I Human chr1 - 1806739 1806739 1806739 GAACTCCTGACCTCATGTGATCTGCCCACCTCAGCCTCCCAAAGTGCTGGGATTACAAACGTGAG GAACTCCTGACCTCATGTGATCTGCCCACCTCCGCCTCCCAAAGTGCTGGGATTACAAACGTGAG T G GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1397437239 Functional Loss SNV dbSNP153 33..33 33 - - - 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_3112,RMVar_hsa_circ_128404,RMVar_hsa_circ_100327,RMVar_hsa_circ_375577,RMVar_hsa_circ_324378,RMVar_hsa_circ_128416,RMVar_hsa_circ_83173,RMVar_hsa_circ_128412,RMVar_hsa_circ_281145,RMVar_hsa_circ_317907,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_300397,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_128422,RMVar_hsa_circ_293069,RMVar_hsa_circ_324871,RMVar_hsa_circ_273354,RMVar_hsa_circ_128426,RMVar_hsa_circ_128427,RMVar_hsa_circ_128424 12329 RMVar_ID_12329 Human_SNP_ID_456728 A-to-I Human chr1 - 1806810 1806809 1806810 ACTACCATGCCCGGCTAATTTTTGTATTTTTAATAGAGACAGGGTTTCGCCATGCTGGCCAGGCT ACTACCATGCCCGGCTAATTTTTGTATTTTTA_TAGAGACAGGGTTTCGCCATGCTGGCCAGGCT AT A GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1445353993 Functional Loss DEL dbSNP153 33..33 33 - - - 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_3112,RMVar_hsa_circ_128404,RMVar_hsa_circ_100327,RMVar_hsa_circ_375577,RMVar_hsa_circ_324378,RMVar_hsa_circ_128416,RMVar_hsa_circ_83173,RMVar_hsa_circ_128412,RMVar_hsa_circ_281145,RMVar_hsa_circ_317907,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_300397,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_128422,RMVar_hsa_circ_293069,RMVar_hsa_circ_324871,RMVar_hsa_circ_273354,RMVar_hsa_circ_128426,RMVar_hsa_circ_128427,RMVar_hsa_circ_128424 12330 RMVar_ID_12330 Human_SNP_ID_456729 A-to-I Human chr1 - 1806817 1806817 1806817 GAGACGCACTACCATGCCCGGCTAATTTTTGTATTTTTAATAGAGACAGGGTTTCGCCATGCTGG GAGACGCACTACCATGCCCGGCTAATTTTTGTGTTTTTAATAGAGACAGGGTTTCGCCATGCTGG T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs916159789 Functional Loss SNV dbSNP153 33..33 33 - - - 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_3112,RMVar_hsa_circ_128404,RMVar_hsa_circ_100327,RMVar_hsa_circ_375577,RMVar_hsa_circ_324378,RMVar_hsa_circ_128416,RMVar_hsa_circ_83173,RMVar_hsa_circ_128412,RMVar_hsa_circ_281145,RMVar_hsa_circ_317907,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_300397,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_128422,RMVar_hsa_circ_293069,RMVar_hsa_circ_324871,RMVar_hsa_circ_273354,RMVar_hsa_circ_128426,RMVar_hsa_circ_128427,RMVar_hsa_circ_128424 12331 RMVar_ID_12331 Human_SNP_ID_456880 A-to-I Human chr1 - 1807382 1807382 1807382 TTGGCTCACTGCAACCCCCGCCTCCTGGGTTCAAGCAGTTTTCCCACCTCAGCCTCCTGAGTAGC TTGGCTCACTGCAACCCCCGCCTCCTGGGTTCGAGCAGTTTTCCCACCTCAGCCTCCTGAGTAGC T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1269266551 Functional Loss SNV dbSNP153 33..33 33 - - - 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_3112,RMVar_hsa_circ_128404,RMVar_hsa_circ_100327,RMVar_hsa_circ_375577,RMVar_hsa_circ_324378,RMVar_hsa_circ_128416,RMVar_hsa_circ_83173,RMVar_hsa_circ_128412,RMVar_hsa_circ_281145,RMVar_hsa_circ_317907,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_300397,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_128422,RMVar_hsa_circ_293069,RMVar_hsa_circ_324871,RMVar_hsa_circ_273354,RMVar_hsa_circ_128426,RMVar_hsa_circ_128427,RMVar_hsa_circ_128424 12332 RMVar_ID_12332 Human_SNP_ID_456892 A-to-I Human chr1 - 1807417 1807417 1807417 CTCTGTTGCCCAGGCTAGAGTGCAGTGGCGCAATCTTGGCTCACTGCAACCCCCGCCTCCTGGGT CTCTGTTGCCCAGGCTAGAGTGCAGTGGCGCAGTCTTGGCTCACTGCAACCCCCGCCTCCTGGGT T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1029749988 Functional Loss SNV dbSNP153 33..33 33 - - - 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_3112,RMVar_hsa_circ_128404,RMVar_hsa_circ_100327,RMVar_hsa_circ_375577,RMVar_hsa_circ_324378,RMVar_hsa_circ_128416,RMVar_hsa_circ_83173,RMVar_hsa_circ_128412,RMVar_hsa_circ_281145,RMVar_hsa_circ_317907,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_300397,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_128422,RMVar_hsa_circ_293069,RMVar_hsa_circ_324871,RMVar_hsa_circ_273354,RMVar_hsa_circ_128426,RMVar_hsa_circ_128427,RMVar_hsa_circ_128424 12333 RMVar_ID_12333 Human_SNP_ID_457399 A-to-I Human chr1 - 1808895 1808895 1808895 TTATGTCTGTAATCCCAACACTTTGGGAGGCCAAGGTGGGCGGATCACTTGAGGCCAGGAGTTGG TTATGTCTGTAATCCCAACACTTTGGGAGGCCGAGGTGGGCGGATCACTTGAGGCCAGGAGTTGG T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs920673242 Functional Loss SNV dbSNP153 33..33 33 - - - 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_3112,RMVar_hsa_circ_128404,RMVar_hsa_circ_100327,RMVar_hsa_circ_375577,RMVar_hsa_circ_324378,RMVar_hsa_circ_128416,RMVar_hsa_circ_83173,RMVar_hsa_circ_128412,RMVar_hsa_circ_281145,RMVar_hsa_circ_317907,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_300397,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_128422,RMVar_hsa_circ_293069,RMVar_hsa_circ_324871,RMVar_hsa_circ_273354,RMVar_hsa_circ_128426,RMVar_hsa_circ_128427,RMVar_hsa_circ_128424 12334 RMVar_ID_12334 Human_SNP_ID_457404 A-to-I Human chr1 - 1808916 1808916 1808916 TGTGTTTTGAGGCGCTGTGGCTTATGTCTGTAATCCCAACACTTTGGGAGGCCAAGGTGGGCGGA TGTGTTTTGAGGCGCTGTGGCTTATGTCTGTAGTCCCAACACTTTGGGAGGCCAAGGTGGGCGGA T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1188107502 Functional Loss SNV dbSNP153 33..33 33 - - - 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_3112,RMVar_hsa_circ_128404,RMVar_hsa_circ_100327,RMVar_hsa_circ_375577,RMVar_hsa_circ_324378,RMVar_hsa_circ_128416,RMVar_hsa_circ_83173,RMVar_hsa_circ_128412,RMVar_hsa_circ_281145,RMVar_hsa_circ_317907,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_300397,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_128422,RMVar_hsa_circ_293069,RMVar_hsa_circ_324871,RMVar_hsa_circ_273354,RMVar_hsa_circ_128426,RMVar_hsa_circ_128427,RMVar_hsa_circ_128424 12335 RMVar_ID_12335 Human_SNP_ID_457954 A-to-I Human chr1 - 1810805 1810805 1810805 AAGTTAACTAGGCTTCATGGTGGGTGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGATAA AAGTTAACTAGGCTTCATGGTGGGTGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGATAA T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1184478772 Functional Loss SNV dbSNP153 33..33 33 - - - 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_3112,RMVar_hsa_circ_128404,RMVar_hsa_circ_100327,RMVar_hsa_circ_375577,RMVar_hsa_circ_324378,RMVar_hsa_circ_128416,RMVar_hsa_circ_83173,RMVar_hsa_circ_128412,RMVar_hsa_circ_281145,RMVar_hsa_circ_317907,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_300397,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_128422,RMVar_hsa_circ_293069,RMVar_hsa_circ_324871,RMVar_hsa_circ_273354,RMVar_hsa_circ_128426,RMVar_hsa_circ_128427,RMVar_hsa_circ_128424 12336 RMVar_ID_12336 Human_SNP_ID_457990 A-to-I Human chr1 - 1810943 1810943 1810943 ACATGAGAGGCCAGGCACCGTGGTTCACGCCTATAATCCCAGCACTTTGGGAGGCTAAGGCGGGT ACATGAGAGGCCAGGCACCGTGGTTCACGCCTGTAATCCCAGCACTTTGGGAGGCTAAGGCGGGT T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1211380110 Functional Loss SNV dbSNP153 33..33 33 - - - 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_3112,RMVar_hsa_circ_128404,RMVar_hsa_circ_100327,RMVar_hsa_circ_375577,RMVar_hsa_circ_324378,RMVar_hsa_circ_128416,RMVar_hsa_circ_83173,RMVar_hsa_circ_128412,RMVar_hsa_circ_281145,RMVar_hsa_circ_317907,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_300397,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_128422,RMVar_hsa_circ_293069,RMVar_hsa_circ_324871,RMVar_hsa_circ_273354,RMVar_hsa_circ_128426,RMVar_hsa_circ_128427,RMVar_hsa_circ_128424 12337 RMVar_ID_12337 Human_SNP_ID_458111 A-to-I Human chr1 - 1811209 1811208 1811210 GTGGCGAGTGCCTGTAGTTTCAGCTGCACTCAAGAGGCTGAGGTGGGAGAATCGCTTGAACCCAG GTGGCGAGTGCCTGTAGTTTCAGCTGCACTC__GAGGCTGAGGTGGGAGAATCGCTTGAACCCAG CTT C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1220513397 Functional Loss DEL dbSNP153 32..33 33 - - - 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_3112,RMVar_hsa_circ_128404,RMVar_hsa_circ_100327,RMVar_hsa_circ_375577,RMVar_hsa_circ_324378,RMVar_hsa_circ_128416,RMVar_hsa_circ_83173,RMVar_hsa_circ_128412,RMVar_hsa_circ_281145,RMVar_hsa_circ_317907,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_300397,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_128422,RMVar_hsa_circ_293069,RMVar_hsa_circ_324871,RMVar_hsa_circ_273354,RMVar_hsa_circ_128426,RMVar_hsa_circ_128427,RMVar_hsa_circ_128424 12338 RMVar_ID_12338 Human_SNP_ID_458112 A-to-I Human chr1 - 1811209 1811208 1811209 GTGGCGAGTGCCTGTAGTTTCAGCTGCACTCAAGAGGCTGAGGTGGGAGAATCGCTTGAACCCAG GTGGCGAGTGCCTGTAGTTTCAGCTGCACTCA_GAGGCTGAGGTGGGAGAATCGCTTGAACCCAG CT C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1341170202 Functional Loss DEL dbSNP153 33..33 33 - - - 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_3112,RMVar_hsa_circ_128404,RMVar_hsa_circ_100327,RMVar_hsa_circ_375577,RMVar_hsa_circ_324378,RMVar_hsa_circ_128416,RMVar_hsa_circ_83173,RMVar_hsa_circ_128412,RMVar_hsa_circ_281145,RMVar_hsa_circ_317907,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_300397,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_128422,RMVar_hsa_circ_293069,RMVar_hsa_circ_324871,RMVar_hsa_circ_273354,RMVar_hsa_circ_128426,RMVar_hsa_circ_128427,RMVar_hsa_circ_128424 12339 RMVar_ID_12339 Human_SNP_ID_458252 A-to-I Human chr1 - 1811620 1811620 1811620 GCTGTCTTAGCTCACTGCAAGCTCTGCCTCCCAGGTTAACACCATTCTCCTGCCTCAGCCTCCCG GCTGTCTTAGCTCACTGCAAGCTCTGCCTCCCGGGTTAACACCATTCTCCTGCCTCAGCCTCCCG T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs951532039 Functional Loss SNV dbSNP153 33..33 33 - - - 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_3112,RMVar_hsa_circ_128404,RMVar_hsa_circ_100327,RMVar_hsa_circ_375577,RMVar_hsa_circ_324378,RMVar_hsa_circ_128416,RMVar_hsa_circ_83173,RMVar_hsa_circ_128412,RMVar_hsa_circ_281145,RMVar_hsa_circ_317907,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_300397,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_128422,RMVar_hsa_circ_293069,RMVar_hsa_circ_324871,RMVar_hsa_circ_273354,RMVar_hsa_circ_128426,RMVar_hsa_circ_128427,RMVar_hsa_circ_128424 12340 RMVar_ID_12340 Human_SNP_ID_458265 A-to-I Human chr1 - 1811665 1811665 1811665 TTTTGAGACGGAGTCTCACTGTCGCCCAGGCTAGAGTGCAATGGTGCTGTCTTAGCTCACTGCAA TTTTGAGACGGAGTCTCACTGTCGCCCAGGCTGGAGTGCAATGGTGCTGTCTTAGCTCACTGCAA T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1249652521 Functional Loss SNV dbSNP153 33..33 33 - - - 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_3112,RMVar_hsa_circ_128404,RMVar_hsa_circ_100327,RMVar_hsa_circ_375577,RMVar_hsa_circ_324378,RMVar_hsa_circ_128416,RMVar_hsa_circ_83173,RMVar_hsa_circ_128412,RMVar_hsa_circ_281145,RMVar_hsa_circ_317907,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_300397,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_128422,RMVar_hsa_circ_293069,RMVar_hsa_circ_324871,RMVar_hsa_circ_273354,RMVar_hsa_circ_128426,RMVar_hsa_circ_128427,RMVar_hsa_circ_128424 12341 RMVar_ID_12341 Human_SNP_ID_458775 A-to-I Human chr1 - 1813253 1813253 1813253 AAATTTAAAAATTAGCTGGGCATGGTAGCTGTAGTCCCAGCTACTTGGAAGGCTGAGGCACGTGG AAATTTAAAAATTAGCTGGGCATGGTAGCTGTGGTCCCAGCTACTTGGAAGGCTGAGGCACGTGG T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1321598514 Functional Loss SNV dbSNP153 33..33 33 - - - 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_3112,RMVar_hsa_circ_128404,RMVar_hsa_circ_100327,RMVar_hsa_circ_375577,RMVar_hsa_circ_324378,RMVar_hsa_circ_128416,RMVar_hsa_circ_83173,RMVar_hsa_circ_128412,RMVar_hsa_circ_281145,RMVar_hsa_circ_317907,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_300397,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_128422,RMVar_hsa_circ_293069,RMVar_hsa_circ_324871,RMVar_hsa_circ_273354,RMVar_hsa_circ_128426,RMVar_hsa_circ_128427,RMVar_hsa_circ_128424 12342 RMVar_ID_12342 Human_SNP_ID_461264 A-to-I Human chr1 - 1821925 1821925 1821925 CACCATGTTGCCCCAGCTGGTCTTGAACTCCTAGGGCTCAAGGGATCTTCCCGCCTCAGCCTCCC CACCATGTTGCCCCAGCTGGTCTTGAACTCCTGGGGCTCAAGGGATCTTCCCGCCTCAGCCTCCC T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7542340 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17556845 RMVar_hsa_circ_41253,RMVar_hsa_circ_92329,RMVar_hsa_circ_122805,RMVar_hsa_circ_128392,RMVar_hsa_circ_128393,RMVar_hsa_circ_311382,RMVar_hsa_circ_369314,RMVar_hsa_circ_128399,RMVar_hsa_circ_128400,RMVar_hsa_circ_306773,RMVar_hsa_circ_128405,RMVar_hsa_circ_100327,RMVar_hsa_circ_128431,RMVar_hsa_circ_83173,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_128418,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128419,RMVar_hsa_circ_293069,RMVar_hsa_circ_273354,RMVar_hsa_circ_128426,RMVar_hsa_circ_128427,RMVar_hsa_circ_275919,RMVar_hsa_circ_270257,RMVar_hsa_circ_128432,RMVar_hsa_circ_128433,RMVar_hsa_circ_128430,RMVar_hsa_circ_358600,RMVar_hsa_circ_339557,RMVar_hsa_circ_128434 12343 RMVar_ID_12343 Human_SNP_ID_461412 A-to-I Human chr1 - 1822441 1822441 1822441 ATTAGCCAGGTGTGGTGGTGGTGGGCGCCTGTAGTCCCAACTACTTGGGAGGCTGAGGCAGGGAA ATTAGCCAGGTGTGGTGGTGGTGGGCGCCTGTCGTCCCAACTACTTGGGAGGCTGAGGCAGGGAA T G GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1026132678 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41253,RMVar_hsa_circ_92329,RMVar_hsa_circ_122805,RMVar_hsa_circ_128392,RMVar_hsa_circ_128393,RMVar_hsa_circ_311382,RMVar_hsa_circ_369314,RMVar_hsa_circ_128399,RMVar_hsa_circ_128400,RMVar_hsa_circ_306773,RMVar_hsa_circ_128405,RMVar_hsa_circ_100327,RMVar_hsa_circ_128431,RMVar_hsa_circ_83173,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_128418,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128419,RMVar_hsa_circ_293069,RMVar_hsa_circ_273354,RMVar_hsa_circ_128426,RMVar_hsa_circ_128427,RMVar_hsa_circ_275919,RMVar_hsa_circ_270257,RMVar_hsa_circ_128432,RMVar_hsa_circ_128433,RMVar_hsa_circ_128430,RMVar_hsa_circ_358600,RMVar_hsa_circ_339557,RMVar_hsa_circ_128434 12344 RMVar_ID_12344 Human_SNP_ID_461845 A-to-I Human chr1 - 1823938 1823938 1823938 CACTTGAGCCCAGGAGGTTGAGGCTGTATAGTAAGCTGTGATTGCACCACTGCACTGCAGCCTAG CACTTGAGCCCAGGAGGTTGAGGCTGTATAGTGAGCTGTGATTGCACCACTGCACTGCAGCCTAG T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs114872616 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10663744 RMVar_hsa_circ_41253,RMVar_hsa_circ_92329,RMVar_hsa_circ_122805,RMVar_hsa_circ_128392,RMVar_hsa_circ_128393,RMVar_hsa_circ_311382,RMVar_hsa_circ_369314,RMVar_hsa_circ_128399,RMVar_hsa_circ_128400,RMVar_hsa_circ_306773,RMVar_hsa_circ_128405,RMVar_hsa_circ_100327,RMVar_hsa_circ_128431,RMVar_hsa_circ_83173,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_128418,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128419,RMVar_hsa_circ_293069,RMVar_hsa_circ_273354,RMVar_hsa_circ_128426,RMVar_hsa_circ_128427,RMVar_hsa_circ_275919,RMVar_hsa_circ_270257,RMVar_hsa_circ_128432,RMVar_hsa_circ_128433,RMVar_hsa_circ_128430,RMVar_hsa_circ_358600,RMVar_hsa_circ_339557,RMVar_hsa_circ_128434 12345 RMVar_ID_12345 Human_SNP_ID_461850 A-to-I Human chr1 - 1823969 1823969 1823969 CGCGCCTGTAGTCTGAGCTACCCAGGAGGATCACTTGAGCCCAGGAGGTTGAGGCTGTATAGTAA CGCGCCTGTAGTCTGAGCTACCCAGGAGGATCGCTTGAGCCCAGGAGGTTGAGGCTGTATAGTAA T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs923803037 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10663744 RMVar_hsa_circ_41253,RMVar_hsa_circ_92329,RMVar_hsa_circ_122805,RMVar_hsa_circ_128392,RMVar_hsa_circ_128393,RMVar_hsa_circ_311382,RMVar_hsa_circ_369314,RMVar_hsa_circ_128399,RMVar_hsa_circ_128400,RMVar_hsa_circ_306773,RMVar_hsa_circ_128405,RMVar_hsa_circ_100327,RMVar_hsa_circ_128431,RMVar_hsa_circ_83173,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_128418,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128419,RMVar_hsa_circ_293069,RMVar_hsa_circ_273354,RMVar_hsa_circ_128426,RMVar_hsa_circ_128427,RMVar_hsa_circ_275919,RMVar_hsa_circ_270257,RMVar_hsa_circ_128432,RMVar_hsa_circ_128433,RMVar_hsa_circ_128430,RMVar_hsa_circ_358600,RMVar_hsa_circ_339557,RMVar_hsa_circ_128434 12346 RMVar_ID_12346 Human_SNP_ID_461859 A-to-I Human chr1 - 1824010 1824010 1824010 TACATACCTAAATAACAGTTTATAAGCTGGGTATGGTGGTGCGCGCCTGTAGTCTGAGCTACCCA TACATACCTAAATAACAGTTTATAAGCTGGGTGTGGTGGTGCGCGCCTGTAGTCTGAGCTACCCA T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs962864723 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41253,RMVar_hsa_circ_92329,RMVar_hsa_circ_122805,RMVar_hsa_circ_128392,RMVar_hsa_circ_128393,RMVar_hsa_circ_311382,RMVar_hsa_circ_369314,RMVar_hsa_circ_128399,RMVar_hsa_circ_128400,RMVar_hsa_circ_306773,RMVar_hsa_circ_128405,RMVar_hsa_circ_100327,RMVar_hsa_circ_128431,RMVar_hsa_circ_83173,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_128418,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128419,RMVar_hsa_circ_293069,RMVar_hsa_circ_273354,RMVar_hsa_circ_128426,RMVar_hsa_circ_128427,RMVar_hsa_circ_275919,RMVar_hsa_circ_270257,RMVar_hsa_circ_128432,RMVar_hsa_circ_128433,RMVar_hsa_circ_128430,RMVar_hsa_circ_358600,RMVar_hsa_circ_339557,RMVar_hsa_circ_128434 12347 RMVar_ID_12347 Human_SNP_ID_462037 A-to-I Human chr1 - 1824773 1824773 1824773 GGTCGGGAGTTCGAGACCAGCCAGGGCAACATAGTGAAACCCCCATCTCTACAAAAAATATAAAA GGTCGGGAGTTCGAGACCAGCCAGGGCAACATGGTGAAACCCCCATCTCTACAAAAAATATAAAA T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs368875803 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41253,RMVar_hsa_circ_92329,RMVar_hsa_circ_122805,RMVar_hsa_circ_128392,RMVar_hsa_circ_128393,RMVar_hsa_circ_311382,RMVar_hsa_circ_369314,RMVar_hsa_circ_128399,RMVar_hsa_circ_128400,RMVar_hsa_circ_306773,RMVar_hsa_circ_128405,RMVar_hsa_circ_100327,RMVar_hsa_circ_128431,RMVar_hsa_circ_83173,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_128418,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128419,RMVar_hsa_circ_293069,RMVar_hsa_circ_273354,RMVar_hsa_circ_128426,RMVar_hsa_circ_128427,RMVar_hsa_circ_275919,RMVar_hsa_circ_270257,RMVar_hsa_circ_128432,RMVar_hsa_circ_128433,RMVar_hsa_circ_128430,RMVar_hsa_circ_358600,RMVar_hsa_circ_339557,RMVar_hsa_circ_128434 12348 RMVar_ID_12348 Human_SNP_ID_463804 A-to-I Human chr1 - 1831259 1831258 1831260 TATCATAGCTCACTGCAGCCTTGAACTCCTGGACTCAAGCGATCCTCCCACCTCAGCCTCCCAAG TATCATAGCTCACTGCAGCCTTGAACTCCTG__CTCAAGCGATCCTCCCACCTCAGCCTCCCAAG GTC G GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1193189737 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_122805,RMVar_hsa_circ_128393,RMVar_hsa_circ_369314,RMVar_hsa_circ_128400,RMVar_hsa_circ_306773,RMVar_hsa_circ_128405,RMVar_hsa_circ_128431,RMVar_hsa_circ_83173,RMVar_hsa_circ_128414,RMVar_hsa_circ_278200,RMVar_hsa_circ_276555,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128419,RMVar_hsa_circ_273354,RMVar_hsa_circ_128427,RMVar_hsa_circ_275919,RMVar_hsa_circ_128432,RMVar_hsa_circ_128433,RMVar_hsa_circ_339557,RMVar_hsa_circ_128436,RMVar_hsa_circ_273994,RMVar_hsa_circ_128435 12349 RMVar_ID_12349 Human_SNP_ID_463805 A-to-I Human chr1 - 1831259 1831259 1831259 TATCATAGCTCACTGCAGCCTTGAACTCCTGGACTCAAGCGATCCTCCCACCTCAGCCTCCCAAG TATCATAGCTCACTGCAGCCTTGAACTCCTGGGCTCAAGCGATCCTCCCACCTCAGCCTCCCAAG T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6603796 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122805,RMVar_hsa_circ_128393,RMVar_hsa_circ_369314,RMVar_hsa_circ_128400,RMVar_hsa_circ_306773,RMVar_hsa_circ_128405,RMVar_hsa_circ_128431,RMVar_hsa_circ_83173,RMVar_hsa_circ_128414,RMVar_hsa_circ_278200,RMVar_hsa_circ_276555,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128419,RMVar_hsa_circ_273354,RMVar_hsa_circ_128427,RMVar_hsa_circ_275919,RMVar_hsa_circ_128432,RMVar_hsa_circ_128433,RMVar_hsa_circ_339557,RMVar_hsa_circ_128436,RMVar_hsa_circ_273994,RMVar_hsa_circ_128435 12350 RMVar_ID_12350 Human_SNP_ID_463806 A-to-I Human chr1 - 1831259 1831259 1831259 TATCATAGCTCACTGCAGCCTTGAACTCCTGGACTCAAGCGATCCTCCCACCTCAGCCTCCCAAG TATCATAGCTCACTGCAGCCTTGAACTCCTGGCCTCAAGCGATCCTCCCACCTCAGCCTCCCAAG T G GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6603796 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122805,RMVar_hsa_circ_128393,RMVar_hsa_circ_369314,RMVar_hsa_circ_128400,RMVar_hsa_circ_306773,RMVar_hsa_circ_128405,RMVar_hsa_circ_128431,RMVar_hsa_circ_83173,RMVar_hsa_circ_128414,RMVar_hsa_circ_278200,RMVar_hsa_circ_276555,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128419,RMVar_hsa_circ_273354,RMVar_hsa_circ_128427,RMVar_hsa_circ_275919,RMVar_hsa_circ_128432,RMVar_hsa_circ_128433,RMVar_hsa_circ_339557,RMVar_hsa_circ_128436,RMVar_hsa_circ_273994,RMVar_hsa_circ_128435 12351 RMVar_ID_12351 Human_SNP_ID_464545 A-to-I Human chr1 - 1834144 1834144 1834144 AGTTCCTGCCCTTCCCCCAGTTGCCAGCGTCTAATGGGTGAGTGAGCTCACTTGTGACTGGGACA AGTTCCTGCCCTTCCCCCAGTTGCCAGCGTCTTATGGGTGAGTGAGCTCACTTGTGACTGGGACA T A GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6603797 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17102659 GWAS_ID_990,GWAS_ID_991,GWAS_ID_992 RMVar_hsa_circ_122805,RMVar_hsa_circ_128393,RMVar_hsa_circ_369314,RMVar_hsa_circ_128400,RMVar_hsa_circ_306773,RMVar_hsa_circ_128405,RMVar_hsa_circ_128431,RMVar_hsa_circ_83173,RMVar_hsa_circ_128414,RMVar_hsa_circ_278200,RMVar_hsa_circ_276555,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128419,RMVar_hsa_circ_273354,RMVar_hsa_circ_128427,RMVar_hsa_circ_275919,RMVar_hsa_circ_128432,RMVar_hsa_circ_128433,RMVar_hsa_circ_339557,RMVar_hsa_circ_128436,RMVar_hsa_circ_273994,RMVar_hsa_circ_128437,RMVar_hsa_circ_128435 12352 RMVar_ID_12352 Human_SNP_ID_464546 A-to-I Human chr1 - 1834144 1834144 1834144 AGTTCCTGCCCTTCCCCCAGTTGCCAGCGTCTAATGGGTGAGTGAGCTCACTTGTGACTGGGACA AGTTCCTGCCCTTCCCCCAGTTGCCAGCGTCTGATGGGTGAGTGAGCTCACTTGTGACTGGGACA T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6603797 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17102659 GWAS_ID_990,GWAS_ID_991,GWAS_ID_992 RMVar_hsa_circ_122805,RMVar_hsa_circ_128393,RMVar_hsa_circ_369314,RMVar_hsa_circ_128400,RMVar_hsa_circ_306773,RMVar_hsa_circ_128405,RMVar_hsa_circ_128431,RMVar_hsa_circ_83173,RMVar_hsa_circ_128414,RMVar_hsa_circ_278200,RMVar_hsa_circ_276555,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128419,RMVar_hsa_circ_273354,RMVar_hsa_circ_128427,RMVar_hsa_circ_275919,RMVar_hsa_circ_128432,RMVar_hsa_circ_128433,RMVar_hsa_circ_339557,RMVar_hsa_circ_128436,RMVar_hsa_circ_273994,RMVar_hsa_circ_128437,RMVar_hsa_circ_128435 12353 RMVar_ID_12353 Human_SNP_ID_465084 A-to-I Human chr1 - 1836051 1836051 1836051 GGGTCTCACTCTGTCTCTTAGACTGGAGTACAATGGTGTGATCATAGCTGACTGCATCCATGACC GGGTCTCACTCTGTCTCTTAGACTGGAGTACAGTGGTGTGATCATAGCTGACTGCATCCATGACC T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs754951544 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10667531 RMVar_hsa_circ_122805,RMVar_hsa_circ_128393,RMVar_hsa_circ_369314,RMVar_hsa_circ_128400,RMVar_hsa_circ_306773,RMVar_hsa_circ_128405,RMVar_hsa_circ_128431,RMVar_hsa_circ_83173,RMVar_hsa_circ_128414,RMVar_hsa_circ_278200,RMVar_hsa_circ_276555,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128419,RMVar_hsa_circ_273354,RMVar_hsa_circ_128427,RMVar_hsa_circ_275919,RMVar_hsa_circ_128432,RMVar_hsa_circ_128433,RMVar_hsa_circ_339557,RMVar_hsa_circ_128436,RMVar_hsa_circ_273994,RMVar_hsa_circ_128437,RMVar_hsa_circ_128435 12354 RMVar_ID_12354 Human_SNP_ID_465596 A-to-I Human chr1 - 1837652 1837652 1837652 AGGAGGTTGAGGCAGGGGAATCGCTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCTGAGATTGCA AGGAGGTTGAGGCAGGGGAATCGCTTGAACCCGGGAGGCAGAGGTTGCAGTGAGCTGAGATTGCA T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1317216154 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122805,RMVar_hsa_circ_128393,RMVar_hsa_circ_369314,RMVar_hsa_circ_128400,RMVar_hsa_circ_306773,RMVar_hsa_circ_128405,RMVar_hsa_circ_128431,RMVar_hsa_circ_83173,RMVar_hsa_circ_128414,RMVar_hsa_circ_278200,RMVar_hsa_circ_276555,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128419,RMVar_hsa_circ_273354,RMVar_hsa_circ_128427,RMVar_hsa_circ_275919,RMVar_hsa_circ_128432,RMVar_hsa_circ_128433,RMVar_hsa_circ_339557,RMVar_hsa_circ_128436,RMVar_hsa_circ_273994,RMVar_hsa_circ_128437,RMVar_hsa_circ_128435 12355 RMVar_ID_12355 Human_SNP_ID_465734 A-to-I Human chr1 - 1838151 1838146 1838151 TTGCCCAGGCCGAAGTGCAGTGGTGCAATCTCAGCTCTCTGCAACCTCCCCCTCCCAGGTTCAAG TTGCCCAGGCCGAAGTGCAGTGGTGCAATCTC_____TCTGCAACCTCCCCCTCCCAGGTTCAAG AGAGCT A GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1271252480 Functional Loss DEL dbSNP153 33..37 33 - - - RMVar_hsa_circ_122805,RMVar_hsa_circ_128393,RMVar_hsa_circ_369314,RMVar_hsa_circ_128400,RMVar_hsa_circ_306773,RMVar_hsa_circ_128405,RMVar_hsa_circ_128431,RMVar_hsa_circ_83173,RMVar_hsa_circ_128414,RMVar_hsa_circ_278200,RMVar_hsa_circ_276555,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128419,RMVar_hsa_circ_273354,RMVar_hsa_circ_128427,RMVar_hsa_circ_275919,RMVar_hsa_circ_128432,RMVar_hsa_circ_128433,RMVar_hsa_circ_339557,RMVar_hsa_circ_128436,RMVar_hsa_circ_273994,RMVar_hsa_circ_128437,RMVar_hsa_circ_128435 12356 RMVar_ID_12356 Human_SNP_ID_465752 A-to-I Human chr1 - 1838197 1838197 1838197 ACAATTGGATATTCTTTTTTTTCTTTTGAGACAGAGTCTTGCTCTGTTGCCCAGGCCGAAGTGCA ACAATTGGATATTCTTTTTTTTCTTTTGAGACGGAGTCTTGCTCTGTTGCCCAGGCCGAAGTGCA T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1165040675 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17556848 RMVar_hsa_circ_122805,RMVar_hsa_circ_128393,RMVar_hsa_circ_369314,RMVar_hsa_circ_128400,RMVar_hsa_circ_306773,RMVar_hsa_circ_128405,RMVar_hsa_circ_128431,RMVar_hsa_circ_83173,RMVar_hsa_circ_128414,RMVar_hsa_circ_278200,RMVar_hsa_circ_276555,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128419,RMVar_hsa_circ_273354,RMVar_hsa_circ_128427,RMVar_hsa_circ_275919,RMVar_hsa_circ_128432,RMVar_hsa_circ_128433,RMVar_hsa_circ_339557,RMVar_hsa_circ_128436,RMVar_hsa_circ_273994,RMVar_hsa_circ_128437,RMVar_hsa_circ_128435 12357 RMVar_ID_12357 Human_SNP_ID_466337 A-to-I Human chr1 - 1840209 1840209 1840209 TTTTTTTTCTTTTCGAGACGGTGTCTTGCTCTATCACCCAGGCTGAAGTGTAGTGGCGTGATCTC TTTTTTTTCTTTTCGAGACGGTGTCTTGCTCTGTCACCCAGGCTGAAGTGTAGTGGCGTGATCTC T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1265006434 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10667615,Human_RBP_ID_23145612,Human_RBP_ID_23347297 RMVar_hsa_circ_83173,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128432,RMVar_hsa_circ_128435,RMVar_hsa_circ_128438,RMVar_hsa_circ_128439 12358 RMVar_ID_12358 Human_SNP_ID_467083 A-to-I Human chr1 - 1842433 1842420 1842433 CAGGACCAGGACTTCTTTTTTTTTTTTTTTTGAGATGGAGTCTCACTCTGTCACCCCGCCCAGGC CAGGACCAGGACTTCTTTTTTTTTTTTTTTTG_____________CTCTGTCACCCCGCCCAGGC GTGAGACTCCATCT G GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1221093585 Functional Loss DEL dbSNP153 33..45 33 - - - Human_RBP_ID_10667937 RMVar_hsa_circ_83173,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128432,RMVar_hsa_circ_128435,RMVar_hsa_circ_128438,RMVar_hsa_circ_128439 12359 RMVar_ID_12359 Human_SNP_ID_468415 A-to-I Human chr1 - 1846419 1846419 1846419 GGGATTACAGGTGCCAGCCACCACGCCTGGCTAATTTTTTTGTTTTTAGCAGAGATGGAGTTTCA GGGATTACAGGTGCCAGCCACCACGCCTGGCTGATTTTTTTGTTTTTAGCAGAGATGGAGTTTCA T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs900821917 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83173,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128432,RMVar_hsa_circ_128435,RMVar_hsa_circ_128438,RMVar_hsa_circ_128439 12360 RMVar_ID_12360 Human_SNP_ID_468416 A-to-I Human chr1 - 1846419 1846419 1846419 GGGATTACAGGTGCCAGCCACCACGCCTGGCTAATTTTTTTGTTTTTAGCAGAGATGGAGTTTCA GGGATTACAGGTGCCAGCCACCACGCCTGGCTCATTTTTTTGTTTTTAGCAGAGATGGAGTTTCA T G GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs900821917 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83173,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128432,RMVar_hsa_circ_128435,RMVar_hsa_circ_128438,RMVar_hsa_circ_128439 12361 RMVar_ID_12361 Human_SNP_ID_468728 A-to-I Human chr1 - 1847597 1847597 1847597 TCTTCAGCAGGATAATCCTTCCAGACTTAAACAATGTTCTGTCTATTGGGATTCTCTTCCATAGC TCTTCAGCAGGATAATCCTTCCAGACTTAAACGATGTTCTGTCTATTGGGATTCTCTTCCATAGC T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6692959 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_993,GWAS_ID_994,GWAS_ID_995 RMVar_hsa_circ_83173,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128432,RMVar_hsa_circ_128435,RMVar_hsa_circ_128438,RMVar_hsa_circ_128439 12362 RMVar_ID_12362 Human_SNP_ID_469270 A-to-I Human chr1 - 1849439 1849439 1849439 TTGTGCCACTGCACTGTAGCCTGGGTGATAGAATGAGACCTAGTCCCACAAAAGACTTCCTCAGA TTGTGCCACTGCACTGTAGCCTGGGTGATAGAGTGAGACCTAGTCCCACAAAAGACTTCCTCAGA T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6603801 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83173,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128432,RMVar_hsa_circ_128435,RMVar_hsa_circ_128439 12363 RMVar_ID_12363 Human_SNP_ID_470197 A-to-I Human chr1 - 1852502 1852501 1852502 TTTGAGGCCGGGCGCCGTGGCTCGAGCCTGTAATCCTAGCACTTTGGGAGACTGAGGCGGGCGGG TTTGAGGCCGGGCGCCGTGGCTCGAGCCTGTA_TCCTAGCACTTTGGGAGACTGAGGCGGGCGGG AT A GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1163306330 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_83173,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128432,RMVar_hsa_circ_128435,RMVar_hsa_circ_128439 12364 RMVar_ID_12364 Human_SNP_ID_470228 A-to-I Human chr1 - 1852579 1852579 1852579 CCAGTCCTCCTGTCTTAGCCTCTGGAGTAGCTAGGACTACAGGTATGCACCACCATGCCAATTTT CCAGTCCTCCTGTCTTAGCCTCTGGAGTAGCTGGGACTACAGGTATGCACCACCATGCCAATTTT T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1295602523 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83173,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128432,RMVar_hsa_circ_128435,RMVar_hsa_circ_128439 12365 RMVar_ID_12365 Human_SNP_ID_470903 A-to-I Human chr1 - 1855133 1855133 1855133 TTTTTTTGAGATACGGTCTTGCTCTGTTGCCCAGGCTGGAGTGCAGTGGAGCTATCTCGGCCCAC TTTTTTTGAGATACGGTCTTGCTCTGTTGCCCGGGCTGGAGTGCAGTGGAGCTATCTCGGCCCAC T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232150252 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23145664 RMVar_hsa_circ_83173,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128432,RMVar_hsa_circ_128435,RMVar_hsa_circ_128439 12366 RMVar_ID_12366 Human_SNP_ID_471061 A-to-I Human chr1 - 1855445 1855445 1855445 CGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCCCGGCCGGGAGTT CGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTGCAGGCGTGAGCCACCGCGCCCGGCCGGGAGTT T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1299560253 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9470266 RMVar_hsa_circ_83173,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128432,RMVar_hsa_circ_128435,RMVar_hsa_circ_128439 12367 RMVar_ID_12367 Human_SNP_ID_471389 A-to-I Human chr1 - 1856323 1856323 1856323 GCCCAGGAGTTGGAGATCTGCCTGGGCAACATAGCGAGACCCCATCTCTAATTTAAAAAAAGAAA GCCCAGGAGTTGGAGATCTGCCTGGGCAACATGGCGAGACCCCATCTCTAATTTAAAAAAAGAAA T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1429036949 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17556855 RMVar_hsa_circ_83173,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128432,RMVar_hsa_circ_128435,RMVar_hsa_circ_128439 12368 RMVar_ID_12368 Human_SNP_ID_473066 A-to-I Human chr1 - 1862122 1862122 1862122 CATCTCCTTGGTTCAAGTGATTGTCCTGCCTTAGCCTCCCAAGTAGCTGGGATTACAGGTGTGCG CATCTCCTTGGTTCAAGTGATTGTCCTGCCTTTGCCTCCCAAGTAGCTGGGATTACAGGTGTGCG T A GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1183610246 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10676298 RMVar_hsa_circ_83173,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128432,RMVar_hsa_circ_128435,RMVar_hsa_circ_128439 12369 RMVar_ID_12369 Human_SNP_ID_474078 A-to-I Human chr1 - 1865464 1865464 1865464 CTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGTGCCCGCCACCACACCTGGCCAATGTTT CTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTTCAGGTGCCCGCCACCACACCTGGCCAATGTTT T A GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs983465102 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83173,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128432,RMVar_hsa_circ_128435,RMVar_hsa_circ_128439 12370 RMVar_ID_12370 Human_SNP_ID_474079 A-to-I Human chr1 - 1865464 1865464 1865464 CTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGTGCCCGCCACCACACCTGGCCAATGTTT CTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTGCAGGTGCCCGCCACCACACCTGGCCAATGTTT T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs983465102 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83173,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128432,RMVar_hsa_circ_128435,RMVar_hsa_circ_128439 12371 RMVar_ID_12371 Human_SNP_ID_474081 A-to-I Human chr1 - 1865474 1865474 1865474 TCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGTGCCCGCCACCACACCTG TCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTTGCTGGGACTACAGGTGCCCGCCACCACACCTG T A GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1290687766 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83173,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128432,RMVar_hsa_circ_128435,RMVar_hsa_circ_128439 12372 RMVar_ID_12372 Human_SNP_ID_474090 A-to-I Human chr1 - 1865503 1865503 1865503 TGGCTCACTGCGACCTCTGCTTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCT TGGCTCACTGCGACCTCTGCTTCCCGGGTTCATGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCT T A GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202685395 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83173,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128432,RMVar_hsa_circ_128435,RMVar_hsa_circ_128439 12373 RMVar_ID_12373 Human_SNP_ID_474964 A-to-I Human chr1 - 1868314 1868314 1868314 AAAATTAGTTGGATGTGGTGGCTCATGCCTGTAATCCCAGCTACGCGGGAGGCTGAGGCAGGAGA AAAATTAGTTGGATGTGGTGGCTCATGCCTGTGATCCCAGCTACGCGGGAGGCTGAGGCAGGAGA T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1281702880 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83173,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128432,RMVar_hsa_circ_128435,RMVar_hsa_circ_128439 12374 RMVar_ID_12374 Human_SNP_ID_475828 A-to-I Human chr1 - 1871296 1871296 1871296 GCCACCATGCCTGGCTAATTTTTGTATTTTTAATAGAGACGGGGTTTCACCATGTTGGTCACGCT GCCACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGTCACGCT T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1393600954 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23349284,Human_RBP_ID_24613303 RMVar_hsa_circ_83173,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128432,RMVar_hsa_circ_128435,RMVar_hsa_circ_128439 12375 RMVar_ID_12375 Human_SNP_ID_475833 A-to-I Human chr1 - 1871336 1871336 1871336 CCTGCCTCAGCCTCTTGAGTAGCTGAGATTATAGATGTGTGCCACCATGCCTGGCTAATTTTTGT CCTGCCTCAGCCTCTTGAGTAGCTGAGATTATGGATGTGTGCCACCATGCCTGGCTAATTTTTGT T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1020530227 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83173,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128432,RMVar_hsa_circ_128435,RMVar_hsa_circ_128439 12376 RMVar_ID_12376 Human_SNP_ID_475846 A-to-I Human chr1 - 1871374 1871374 1871374 CTCACTGCAACCTCCGCCTCCTACGTTCAAGCAATACTCCTGCCTCAGCCTCTTGAGTAGCTGAG CTCACTGCAACCTCCGCCTCCTACGTTCAAGCCATACTCCTGCCTCAGCCTCTTGAGTAGCTGAG T G GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs140075436 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83173,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128432,RMVar_hsa_circ_128435,RMVar_hsa_circ_128439 12377 RMVar_ID_12377 Human_SNP_ID_475848 A-to-I Human chr1 - 1871378 1871378 1871378 TGGGCTCACTGCAACCTCCGCCTCCTACGTTCAAGCAATACTCCTGCCTCAGCCTCTTGAGTAGC TGGGCTCACTGCAACCTCCGCCTCCTACGTTCGAGCAATACTCCTGCCTCAGCCTCTTGAGTAGC T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1490484859 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83173,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128432,RMVar_hsa_circ_128435,RMVar_hsa_circ_128439 12378 RMVar_ID_12378 Human_SNP_ID_476031 A-to-I Human chr1 - 1872059 1872059 1872059 AGTTGGAGTTTGCAGTGAGCTATGATCACACAACTGTACTCGAGTCTGGGCAACAGAGCGAGACC AGTTGGAGTTTGCAGTGAGCTATGATCACACATCTGTACTCGAGTCTGGGCAACAGAGCGAGACC T A GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1207052014 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10682190 RMVar_hsa_circ_83173,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128432,RMVar_hsa_circ_128435,RMVar_hsa_circ_128439 12379 RMVar_ID_12379 Human_SNP_ID_476034 A-to-I Human chr1 - 1872067 1872067 1872067 AGCCCAGGAGTTGGAGTTTGCAGTGAGCTATGATCACACAACTGTACTCGAGTCTGGGCAACAGA AGCCCAGGAGTTGGAGTTTGCAGTGAGCTATGGTCACACAACTGTACTCGAGTCTGGGCAACAGA T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1055028391 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10682190 RMVar_hsa_circ_83173,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128432,RMVar_hsa_circ_128435,RMVar_hsa_circ_128439 12380 RMVar_ID_12380 Human_SNP_ID_476035 A-to-I Human chr1 - 1872070 1872070 1872070 TTCAGCCCAGGAGTTGGAGTTTGCAGTGAGCTATGATCACACAACTGTACTCGAGTCTGGGCAAC TTCAGCCCAGGAGTTGGAGTTTGCAGTGAGCTGTGATCACACAACTGTACTCGAGTCTGGGCAAC T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs767883460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10682190 RMVar_hsa_circ_83173,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128432,RMVar_hsa_circ_128435,RMVar_hsa_circ_128439 12381 RMVar_ID_12381 Human_SNP_ID_476036 A-to-I Human chr1 - 1872070 1872070 1872070 TTCAGCCCAGGAGTTGGAGTTTGCAGTGAGCTATGATCACACAACTGTACTCGAGTCTGGGCAAC TTCAGCCCAGGAGTTGGAGTTTGCAGTGAGCTCTGATCACACAACTGTACTCGAGTCTGGGCAAC T G GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs767883460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10682190 RMVar_hsa_circ_83173,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128432,RMVar_hsa_circ_128435,RMVar_hsa_circ_128439 12382 RMVar_ID_12382 Human_SNP_ID_476044 A-to-I Human chr1 - 1872099 1872099 1872099 TACTGGGGAGGCTGAGGAGGGAGCATCGCTTCAGCCCAGGAGTTGGAGTTTGCAGTGAGCTATGA TACTGGGGAGGCTGAGGAGGGAGCATCGCTTCGGCCCAGGAGTTGGAGTTTGCAGTGAGCTATGA T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1433524761 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83173,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128432,RMVar_hsa_circ_128435,RMVar_hsa_circ_128439 12383 RMVar_ID_12383 Human_SNP_ID_476048 A-to-I Human chr1 - 1872107 1872107 1872107 GTTCCAGCTACTGGGGAGGCTGAGGAGGGAGCATCGCTTCAGCCCAGGAGTTGGAGTTTGCAGTG GTTCCAGCTACTGGGGAGGCTGAGGAGGGAGCGTCGCTTCAGCCCAGGAGTTGGAGTTTGCAGTG T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs993121966 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83173,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128432,RMVar_hsa_circ_128435,RMVar_hsa_circ_128439 12384 RMVar_ID_12384 Human_SNP_ID_476057 A-to-I Human chr1 - 1872148 1872148 1872148 TAAAAGAAAAAATTAGCTGGGCATTGTAGCATACACTTGTAGTTCCAGCTACTGGGGAGGCTGAG TAAAAGAAAAAATTAGCTGGGCATTGTAGCATGCACTTGTAGTTCCAGCTACTGGGGAGGCTGAG T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1009263906 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10682457 RMVar_hsa_circ_83173,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128432,RMVar_hsa_circ_128435,RMVar_hsa_circ_128439 12385 RMVar_ID_12385 Human_SNP_ID_476059 A-to-I Human chr1 - 1872153 1872153 1872153 CTACTTAAAAGAAAAAATTAGCTGGGCATTGTAGCATACACTTGTAGTTCCAGCTACTGGGGAGG CTACTTAAAAGAAAAAATTAGCTGGGCATTGTGGCATACACTTGTAGTTCCAGCTACTGGGGAGG T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1133969 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10682457 RMVar_hsa_circ_83173,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128432,RMVar_hsa_circ_128435,RMVar_hsa_circ_128439 12386 RMVar_ID_12386 Human_SNP_ID_476066 A-to-I Human chr1 - 1872169 1872169 1872169 GTTCAAGACTCTGTCTCTACTTAAAAGAAAAAATTAGCTGGGCATTGTAGCATACACTTGTAGTT GTTCAAGACTCTGTCTCTACTTAAAAGAAAAATTTAGCTGGGCATTGTAGCATACACTTGTAGTT T A GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs527586908 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10682457 RMVar_hsa_circ_83173,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128432,RMVar_hsa_circ_128435,RMVar_hsa_circ_128439 12387 RMVar_ID_12387 Human_SNP_ID_476069 A-to-I Human chr1 - 1872179 1872179 1872179 GAGCCCAGGAGTTCAAGACTCTGTCTCTACTTAAAAGAAAAAATTAGCTGGGCATTGTAGCATAC GAGCCCAGGAGTTCAAGACTCTGTCTCTACTTGAAAGAAAAAATTAGCTGGGCATTGTAGCATAC T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1133968 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83173,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128432,RMVar_hsa_circ_128435,RMVar_hsa_circ_128439 12388 RMVar_ID_12388 Human_SNP_ID_476070 A-to-I Human chr1 - 1872183 1872183 1872183 GCTTGAGCCCAGGAGTTCAAGACTCTGTCTCTACTTAAAAGAAAAAATTAGCTGGGCATTGTAGC GCTTGAGCCCAGGAGTTCAAGACTCTGTCTCTGCTTAAAAGAAAAAATTAGCTGGGCATTGTAGC T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1173890293 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83173,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128432,RMVar_hsa_circ_128435,RMVar_hsa_circ_128439 12389 RMVar_ID_12389 Human_SNP_ID_476481 A-to-I Human chr1 - 1873780 1873780 1873780 GGAGTCTTGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCACCATCTTGGCTCACTGTAACCTCTGC GGAGTCTTGCTCTGTCGCCCAGGCTGGAGTGCCGTGGCACCATCTTGGCTCACTGTAACCTCTGC T G GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1194320828 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17556863 RMVar_hsa_circ_83173,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128432,RMVar_hsa_circ_128435,RMVar_hsa_circ_128439 12390 RMVar_ID_12390 Human_SNP_ID_476635 A-to-I Human chr1 - 1874297 1874295 1874297 CCCGGCCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTTGCCATGTTGACCAGGCTGCTCTTGA CCCGGCCTAATTTTTGTATTTTTAGTAGAGAC__GGTTTTGCCATGTTGACCAGGCTGCTCTTGA CCT C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1010594957 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_83173,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128432,RMVar_hsa_circ_128435,RMVar_hsa_circ_128439 12391 RMVar_ID_12391 Human_SNP_ID_476636 A-to-I Human chr1 - 1874297 1874297 1874297 CCCGGCCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTTGCCATGTTGACCAGGCTGCTCTTGA CCCGGCCTAATTTTTGTATTTTTAGTAGAGACTGGGTTTTGCCATGTTGACCAGGCTGCTCTTGA T A GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1048381913 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83173,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128432,RMVar_hsa_circ_128435,RMVar_hsa_circ_128439 12392 RMVar_ID_12392 Human_SNP_ID_476658 A-to-I Human chr1 - 1874358 1874358 1874358 GCAGTCCGCCCGCCTCAGCCTCCCAAAGTGCTAGGATTACAGACACGCGTGAGCCACCACGCCCG GCAGTCCGCCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGACACGCGTGAGCCACCACGCCCG T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs941256437 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10684176,Human_RBP_ID_23145804 RMVar_hsa_circ_83173,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128432,RMVar_hsa_circ_128435,RMVar_hsa_circ_128439 12393 RMVar_ID_12393 Human_SNP_ID_476706 A-to-I Human chr1 - 1874485 1874485 1874485 CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGTGCACACCGCCACGCCCGGCTTTCTCTG CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTGCAGGTGCACACCGCCACGCCCGGCTTTCTCTG T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1006386764 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83173,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128432,RMVar_hsa_circ_128435,RMVar_hsa_circ_128439 12394 RMVar_ID_12394 Human_SNP_ID_476977 A-to-I Human chr1 - 1875289 1875289 1875289 TACTTGGGAGACTGAGGCATGAGAATCACTTGAACTGGAGAGGTTGAGGTTGCAGTGAGCTGAGA TACTTGGGAGACTGAGGCATGAGAATCACTTGCACTGGAGAGGTTGAGGTTGCAGTGAGCTGAGA T G GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1328313357 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10684569,Human_RBP_ID_24755026 RMVar_hsa_circ_83173,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128432,RMVar_hsa_circ_128435,RMVar_hsa_circ_128439 12395 RMVar_ID_12395 Human_SNP_ID_476979 A-to-I Human chr1 - 1875294 1875294 1875294 CCAGCTACTTGGGAGACTGAGGCATGAGAATCACTTGAACTGGAGAGGTTGAGGTTGCAGTGAGC CCAGCTACTTGGGAGACTGAGGCATGAGAATCCCTTGAACTGGAGAGGTTGAGGTTGCAGTGAGC T G GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs992319027 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10684570,Human_RBP_ID_24613899 RMVar_hsa_circ_83173,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128432,RMVar_hsa_circ_128435,RMVar_hsa_circ_128439 12396 RMVar_ID_12396 Human_SNP_ID_477442 A-to-I Human chr1 - 1876642 1876642 1876642 TCTCCATTGACTGGGTGTGGTGGCTTATGCCTATGACACTTATCACTTTGGGAGGCTGAGGTGGG TCTCCATTGACTGGGTGTGGTGGCTTATGCCTGTGACACTTATCACTTTGGGAGGCTGAGGTGGG T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs185366690 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83173,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128432,RMVar_hsa_circ_128435,RMVar_hsa_circ_128439 12397 RMVar_ID_12397 Human_SNP_ID_477572 A-to-I Human chr1 - 1877178 1877178 1877178 CTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCATACACCACCATGCCTGGCTAATTTTG CTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTGCAGGCATACACCACCATGCCTGGCTAATTTTG T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1298912770 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83173,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128432,RMVar_hsa_circ_128435,RMVar_hsa_circ_128439 12398 RMVar_ID_12398 Human_SNP_ID_477582 A-to-I Human chr1 - 1877223 1877223 1877223 CGATCTCGGCTCATTGAAACCTCCACCTCCCCAGCTCAGGCGATTCTCCTGCCTCAGCCTCCTGA CGATCTCGGCTCATTGAAACCTCCACCTCCCCCGCTCAGGCGATTCTCCTGCCTCAGCCTCCTGA T G GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1318529554 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10685291,Human_RBP_ID_23303039 RMVar_hsa_circ_83173,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128432,RMVar_hsa_circ_128435,RMVar_hsa_circ_128439 12399 RMVar_ID_12399 Human_SNP_ID_477765 A-to-I Human chr1 - 1877610 1877610 1877610 TTAGGGGCTTGGCATGGTGGCTCATGCCTGTAATCTTAGCACTTTGGGAGGCTGAGGCAGGAGAA TTAGGGGCTTGGCATGGTGGCTCATGCCTGTAGTCTTAGCACTTTGGGAGGCTGAGGCAGGAGAA T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs928925692 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19237009 RMVar_hsa_circ_83173,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128432,RMVar_hsa_circ_128435,RMVar_hsa_circ_128439 12400 RMVar_ID_12400 Human_SNP_ID_477771 A-to-I Human chr1 - 1877629 1877629 1877629 AAATGTTCATTGTAGTAAATTAGGGGCTTGGCATGGTGGCTCATGCCTGTAATCTTAGCACTTTG AAATGTTCATTGTAGTAAATTAGGGGCTTGGCGTGGTGGCTCATGCCTGTAATCTTAGCACTTTG T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1311503883 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10685405 RMVar_hsa_circ_83173,RMVar_hsa_circ_128420,RMVar_hsa_circ_128421,RMVar_hsa_circ_128432,RMVar_hsa_circ_128435,RMVar_hsa_circ_128439 12401 RMVar_ID_12401 Human_SNP_ID_478441 A-to-I Human chr1 - 1880092 1880092 1880092 CCCATCTCTACAAAAAAATTTGAAAATTAGCCAGGCATGGTGGTGCGTGCCTGTGGTCCCATCTA CCCATCTCTACAAAAAAATTTGAAAATTAGCCGGGCATGGTGGTGCGTGCCTGTGGTCCCATCTA T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs905892090 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17556864 RMVar_hsa_circ_83173,RMVar_hsa_circ_128421 12402 RMVar_ID_12402 Human_SNP_ID_478443 A-to-I Human chr1 - 1880096 1880096 1880096 AGACCCCATCTCTACAAAAAAATTTGAAAATTAGCCAGGCATGGTGGTGCGTGCCTGTGGTCCCA AGACCCCATCTCTACAAAAAAATTTGAAAATTGGCCAGGCATGGTGGTGCGTGCCTGTGGTCCCA T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1003267158 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17556864 RMVar_hsa_circ_83173,RMVar_hsa_circ_128421 12403 RMVar_ID_12403 Human_SNP_ID_478461 A-to-I Human chr1 - 1880132 1880132 1880132 GGCTGAGATTTTGAGACCAGCCTGGGCAACATAGTGAGACCCCATCTCTACAAAAAAATTTGAAA GGCTGAGATTTTGAGACCAGCCTGGGCAACATGGTGAGACCCCATCTCTACAAAAAAATTTGAAA T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1333384853 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10686980 RMVar_hsa_circ_83173,RMVar_hsa_circ_128421 12404 RMVar_ID_12404 Human_SNP_ID_478940 A-to-I Human chr1 - 1881603 1881603 1881603 TTGAGGTCAGGAGTTTGAGACCAGCCTGGCCAACATGGTGAAACCTTGTCTCTACTAAACATATA TTGAGGTCAGGAGTTTGAGACCAGCCTGGCCAGCATGGTGAAACCTTGTCTCTACTAAACATATA T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs770347007 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83173,RMVar_hsa_circ_128421 12405 RMVar_ID_12405 Human_SNP_ID_478963 A-to-I Human chr1 - 1881672 1881672 1881672 CTTGAGGCCGGGCACAGTGGCTTATGCCTGTAATCCCACCACTTTGGGAGGCCAGGGCGGGCGGA CTTGAGGCCGGGCACAGTGGCTTATGCCTGTAGTCCCACCACTTTGGGAGGCCAGGGCGGGCGGA T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233;GSE107867 cultured B-cells;ASD brains,cerebellum - 24183664,30559470 RNA-Seq:(High) rs1190733608 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10687044 RMVar_hsa_circ_83173,RMVar_hsa_circ_128421 12406 RMVar_ID_12406 Human_SNP_ID_479118 A-to-I Human chr1 - 1882192 1882192 1882192 TGAACTCCTTGGCCTCCCAAAGTGTTAGGATTACAGGCGTGAGCCACTGTGCCTGGCCCCAATTT TGAACTCCTTGGCCTCCCAAAGTGTTAGGATTGCAGGCGTGAGCCACTGTGCCTGGCCCCAATTT T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1255094791 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10687077,Human_RBP_ID_17556866 RMVar_hsa_circ_83173,RMVar_hsa_circ_128421 12407 RMVar_ID_12407 Human_SNP_ID_479140 A-to-I Human chr1 - 1882263 1882263 1882263 CCGCCACGCCTAGCTAATGTTTTTTGTATCTTAGTAGAGATGGTGTTTCACCTTGTTGCCCATGC CCGCCACGCCTAGCTAATGTTTTTTGTATCTTGGTAGAGATGGTGTTTCACCTTGTTGCCCATGC T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs145795340 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10687080,Human_RBP_ID_17556866 RMVar_hsa_circ_83173,RMVar_hsa_circ_128421 12408 RMVar_ID_12408 Human_SNP_ID_479176 A-to-I Human chr1 - 1882352 1882352 1882352 ACGATTTCGGCTCACTGCAACCTCCGCCTCCCAGGTTCAGGCGCTTCTCCTGCCTCAGCCTCCCA ACGATTTCGGCTCACTGCAACCTCCGCCTCCCGGGTTCAGGCGCTTCTCCTGCCTCAGCCTCCCA T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1269305253 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83173,RMVar_hsa_circ_128421 12409 RMVar_ID_12409 Human_SNP_ID_479324 A-to-I Human chr1 - 1882666 1882666 1882666 TGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCACGCCCTGCCCATTTAT TGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTGCAGGCGTGAGCCACCACGCCCTGCCCATTTAT T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1254675238 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83173,RMVar_hsa_circ_128421 12410 RMVar_ID_12410 Human_SNP_ID_479446 A-to-I Human chr1 - 1883056 1883055 1883056 CAACTCCTGGGTTCAAGTGATCCTCCTGCCTTAGCCTCCCAAAATGTTGGGATTATAGATGTGAG CAACTCCTGGGTTCAAGTGATCCTCCTGCCTT_GCCTCCCAAAATGTTGGGATTATAGATGTGAG CT C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1403544180 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_83173,RMVar_hsa_circ_128421 12411 RMVar_ID_12411 Human_SNP_ID_479492 A-to-I Human chr1 - 1883215 1883215 1883215 GAGTGTGGAATGTGATGGTATGATCATGGTTCACTGCAGCCTGGACCTCCTGGGCTCATACGATC GAGTGTGGAATGTGATGGTATGATCATGGTTCGCTGCAGCCTGGACCTCCTGGGCTCATACGATC T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978442211 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10687111,Human_RBP_ID_17556867 RMVar_hsa_circ_83173,RMVar_hsa_circ_128421 12412 RMVar_ID_12412 Human_SNP_ID_479510 A-to-I Human chr1 - 1883275 1883275 1883275 TTTTTTCTTTTTCTTTTTTTTTTTTTTTTGGGACAGGGTTTTGCTGTGTCACCCAGGCTGGAGTG TTTTTTCTTTTTCTTTTTTTTTTTTTTTTGGGGCAGGGTTTTGCTGTGTCACCCAGGCTGGAGTG T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1269153677 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10687114 RMVar_hsa_circ_83173,RMVar_hsa_circ_128421 12413 RMVar_ID_12413 Human_SNP_ID_479845 A-to-I Human chr1 - 1884302 1884302 1884302 GAGGCCGAGGAGGGTGGATCAGCCTGGCCAACATGGAGAAACCCCATCTCTACTAAAAATACAAA GAGGCCGAGGAGGGTGGATCAGCCTGGCCAACGTGGAGAAACCCCATCTCTACTAAAAATACAAA T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1413134706 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83173,RMVar_hsa_circ_128421 12414 RMVar_ID_12414 Human_SNP_ID_479861 A-to-I Human chr1 - 1884344 1884344 1884344 GCCCAGACGCGGTGGCTCACGCCTGTAATTCCAGCACTTTGGGAGGCCGAGGAGGGTGGATCAGC GCCCAGACGCGGTGGCTCACGCCTGTAATTCCGGCACTTTGGGAGGCCGAGGAGGGTGGATCAGC T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1248615679 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83173,RMVar_hsa_circ_128421 12415 RMVar_ID_12415 Human_SNP_ID_479863 A-to-I Human chr1 - 1884350 1884350 1884350 AAATTAGCCCAGACGCGGTGGCTCACGCCTGTAATTCCAGCACTTTGGGAGGCCGAGGAGGGTGG AAATTAGCCCAGACGCGGTGGCTCACGCCTGTGATTCCAGCACTTTGGGAGGCCGAGGAGGGTGG T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1319255892 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24614277 RMVar_hsa_circ_83173,RMVar_hsa_circ_128421 12416 RMVar_ID_12416 Human_SNP_ID_480302 A-to-I Human chr1 - 1885763 1885763 1885763 ACGAGGTCAGGAGATTGAGACCATCCTGGCTAACACGGTGAAACCCCATTGCTACTAAAAATACC ACGAGGTCAGGAGATTGAGACCATCCTGGCTATCACGGTGAAACCCCATTGCTACTAAAAATACC T A GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388374515 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83173,RMVar_hsa_circ_128421 12417 RMVar_ID_12417 Human_SNP_ID_480395 A-to-I Human chr1 - 1886061 1886061 1886061 GTGATCTGCCTGTCTGAGCCTCCCAAAGTTCTAGGATTACAGGCGTGAGCCACCGTGCCCTGCCG GTGATCTGCCTGTCTGAGCCTCCCAAAGTTCTGGGATTACAGGCGTGAGCCACCGTGCCCTGCCG T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1421089568 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17556870 RMVar_hsa_circ_83173,RMVar_hsa_circ_128421 12418 RMVar_ID_12418 Human_SNP_ID_480414 A-to-I Human chr1 - 1886129 1886129 1886129 AAATTTTATTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGACCT AAATTTTATTTTAGTAGAGATGGGGTTTCACCGTGTTGGCCAGGCTGGTCTTGAACTCCTGACCT T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1040473816 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83173,RMVar_hsa_circ_128421 12419 RMVar_ID_12419 Human_SNP_ID_480469 A-to-I Human chr1 - 1886300 1886300 1886300 GAAAGCTTTTTTTGTGAGACAGAGTCCCACTCAGCCACCCAGTCTGGAGTGCAGTGGCGCAATCT GAAAGCTTTTTTTGTGAGACAGAGTCCCACTCGGCCACCCAGTCTGGAGTGCAGTGGCGCAATCT T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs940904770 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23145862 RMVar_hsa_circ_83173,RMVar_hsa_circ_128421 12420 RMVar_ID_12420 Human_SNP_ID_480615 A-to-I Human chr1 - 1886830 1886830 1886830 GTGGTGCTGGGCACCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATGGCAGGAACCCG GTGGTGCTGGGCACCTGTAATCCCAGCTACTCTGGAGGCTGAGGCAGGAGAATGGCAGGAACCCG T A GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs187901491 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17556871 RMVar_hsa_circ_83173,RMVar_hsa_circ_128421 12421 RMVar_ID_12421 Human_SNP_ID_480622 A-to-I Human chr1 - 1886844 1886844 1886844 AAAATTAGCTGGGCGTGGTGCTGGGCACCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA AAAATTAGCTGGGCGTGGTGCTGGGCACCTGTTATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA T A GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs766018671 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83173,RMVar_hsa_circ_128421 12422 RMVar_ID_12422 Human_SNP_ID_480669 A-to-I Human chr1 - 1886992 1886992 1886992 TTAAACTGGTTTGACCGGGCGTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGTC TTAAACTGGTTTGACCGGGCGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGTC T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1449909870 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83173,RMVar_hsa_circ_128421 12423 RMVar_ID_12423 Human_SNP_ID_480859 A-to-I Human chr1 - 1887731 1887731 1887731 GGCGCCTGTAATCCCAGCTACTCGGGAGGTTTAGGCACGGGAATCGCTTGAACCCGGGAGGCAGG GGCGCCTGTAATCCCAGCTACTCGGGAGGTTTGGGCACGGGAATCGCTTGAACCCGGGAGGCAGG T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1219877139 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83173,RMVar_hsa_circ_128421 12424 RMVar_ID_12424 Human_SNP_ID_480877 A-to-I Human chr1 - 1887794 1887794 1887794 TCTGGCCAACATAGCGAAACCTCGTATCTACTAAAAATATTAAAATTAGCCGGCGTGGTGGTGGG TCTGGCCAACATAGCGAAACCTCGTATCTACTTAAAATATTAAAATTAGCCGGCGTGGTGGTGGG T A GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs977596711 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9472395 RMVar_hsa_circ_83173,RMVar_hsa_circ_128421 12425 RMVar_ID_12425 Human_SNP_ID_480886 A-to-I Human chr1 - 1887814 1887814 1887814 GGCTGGGAGTTTGAGACCAGTCTGGCCAACATAGCGAAACCTCGTATCTACTAAAAATATTAAAA GGCTGGGAGTTTGAGACCAGTCTGGCCAACATGGCGAAACCTCGTATCTACTAAAAATATTAAAA T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs367766995 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83173,RMVar_hsa_circ_128421 12426 RMVar_ID_12426 Human_SNP_ID_480901 A-to-I Human chr1 - 1887939 1887936 1887939 CAAGAGACTGCAGAATAGTGTGTGGTTTTTTTATTGTTTGTTTTTAAGAGTAAAACCCACTGGGT CAAGAGACTGCAGAATAGTGTGTGGTTTTTTT___GTTTGTTTTTAAGAGTAAAACCCACTGGGT CAAT C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1210343737 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_83173,RMVar_hsa_circ_128421 12427 RMVar_ID_12427 Human_SNP_ID_480902 A-to-I Human chr1 - 1887939 1887939 1887939 CAAGAGACTGCAGAATAGTGTGTGGTTTTTTTATTGTTTGTTTTTAAGAGTAAAACCCACTGGGT CAAGAGACTGCAGAATAGTGTGTGGTTTTTTTTTTGTTTGTTTTTAAGAGTAAAACCCACTGGGT T A GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6603804 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_996,GWAS_ID_997,GWAS_ID_998 RMVar_hsa_circ_83173,RMVar_hsa_circ_128421 12428 RMVar_ID_12428 Human_SNP_ID_480903 A-to-I Human chr1 - 1887939 1887939 1887939 CAAGAGACTGCAGAATAGTGTGTGGTTTTTTTATTGTTTGTTTTTAAGAGTAAAACCCACTGGGT CAAGAGACTGCAGAATAGTGTGTGGTTTTTTTGTTGTTTGTTTTTAAGAGTAAAACCCACTGGGT T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6603804 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_996,GWAS_ID_997,GWAS_ID_998 RMVar_hsa_circ_83173,RMVar_hsa_circ_128421 12429 RMVar_ID_12429 Human_SNP_ID_480904 A-to-I Human chr1 - 1887939 1887939 1887939 CAAGAGACTGCAGAATAGTGTGTGGTTTTTTTATTGTTTGTTTTTAAGAGTAAAACCCACTGGGT CAAGAGACTGCAGAATAGTGTGTGGTTTTTTTCTTGTTTGTTTTTAAGAGTAAAACCCACTGGGT T G GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6603804 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_996,GWAS_ID_997,GWAS_ID_998 RMVar_hsa_circ_83173,RMVar_hsa_circ_128421 12430 RMVar_ID_12430 Human_SNP_ID_481130 A-to-I Human chr1 - 1888655 1888655 1888655 TTTTGTATTTTTAGTAGAGATAGGGTTTCACCATGTTGGCCAAGCTGGTCTCCAACTCCAGACCT TTTTGTATTTTTAGTAGAGATAGGGTTTCACCGTGTTGGCCAAGCTGGTCTCCAACTCCAGACCT T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs779359333 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83173,RMVar_hsa_circ_128421 12431 RMVar_ID_12431 Human_SNP_ID_487739 A-to-I Human chr1 + 1910197 1910197 1910197 TCAAGCGATCCTCTCACCTCAGGCTCTTGAGCAGCTGGGACCACTGACCACTCCCGGCTGATTTT TCAAGCGATCCTCTCACCTCAGGCTCTTGAGCGGCTGGGACCACTGACCACTCCCGGCTGATTTT A G HSALNG0000204 RNACentral:URS0000EB8F96 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs528038936 Functional Loss SNV dbSNP153 33..33 33 - - - 12432 RMVar_ID_12432 Human_SNP_ID_503017 A-to-I Human chr1 - 1954539 1954539 1954539 AACTCAGGCTGTCTGCCCACCTCAGCCTCCCAAGGTGCTGGATTACAGGCATGAGCCACCTCGCC AACTCAGGCTGTCTGCCCACCTCAGCCTCCCAGGGTGCTGGATTACAGGCATGAGCCACCTCGCC T C CFAP74 Ensembl:ENSG00000142609 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs893385757 Functional Loss SNV dbSNP153 33..33 33 - - - 12433 RMVar_ID_12433 Human_SNP_ID_532553 A-to-I Human chr1 - 2045458 2045458 2045458 TCGGCTCGCTGCAGCCTGGACCTCCTGGGCTCAGGTGATCCTCCCACCTCAGCCTCTTGAGTAGC TCGGCTCGCTGCAGCCTGGACCTCCTGGGCTCCGGTGATCCTCCCACCTCAGCCTCTTGAGTAGC T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs368154223 Functional Loss SNV dbSNP153 33..33 33 - - - 12434 RMVar_ID_12434 Human_SNP_ID_589964 A-to-I Human chr1 + 2218322 2218322 2218322 TCACCCAGGCTGAAGTGCAGTGGCGCGATCTCAGCTCACTGCAACCTCTGCTTCCTGGGTACAAG TCACCCAGGCTGAAGTGCAGTGGCGCGATCTCGGCTCACTGCAACCTCTGCTTCCTGGGTACAAG A G AL590822.1 Ensembl:ENSG00000234396 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs539899736 Functional Loss SNV dbSNP153 33..33 33 - - - 12435 RMVar_ID_12435 Human_SNP_ID_590754 A-to-I Human chr1 + 2221384 2221384 2221384 CCTCCCTCTCTCCCCCTCTCTTTTTTAGAGACAGGGTCTCACTCTGTTGTCCTGGCTGAAGTGCA CCTCCCTCTCTCCCCCTCTCTTTTTTAGAGACGGGGTCTCACTCTGTTGTCCTGGCTGAAGTGCA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1020426888 Functional Loss SNV dbSNP153 33..33 33 - - - 12436 RMVar_ID_12436 Human_SNP_ID_590773 A-to-I Human chr1 + 2221464 2221464 2221464 CTCACTGCAGCCTCGGACTCCTTGGCTCAACCAATCCTCCTTCCTCAGCTTCCTGAGTTGCTGGG CTCACTGCAGCCTCGGACTCCTTGGCTCAACCGATCCTCCTTCCTCAGCTTCCTGAGTTGCTGGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs748908712 Functional Loss SNV dbSNP153 33..33 33 - - - 12437 RMVar_ID_12437 Human_SNP_ID_604735 A-to-I Human chr1 + 2264634 2264634 2264634 ATGTTGGTCAGCCTGGTCTTGAACTTGGACTCAAGCAGTCTGCCCTCCCCAGCTTCCCATAGTGC ATGTTGGTCAGCCTGGTCTTGAACTTGGACTCCAGCAGTCTGCCCTCCCCAGCTTCCCATAGTGC A C SKI Ensembl:ENSG00000157933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1342763472 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10777205 12438 RMVar_ID_12438 Human_SNP_ID_604736 A-to-I Human chr1 + 2264634 2264634 2264634 ATGTTGGTCAGCCTGGTCTTGAACTTGGACTCAAGCAGTCTGCCCTCCCCAGCTTCCCATAGTGC ATGTTGGTCAGCCTGGTCTTGAACTTGGACTCTAGCAGTCTGCCCTCCCCAGCTTCCCATAGTGC A T SKI Ensembl:ENSG00000157933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1342763472 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10777205 12439 RMVar_ID_12439 Human_SNP_ID_604808 A-to-I Human chr1 + 2264835 2264834 2264836 TTTTTTCTTTCTTTCCTTTGTTTTTTTGAGACAGAATCTCACTCTGTCACCCAGGCTGAAGTGCA TTTTTTCTTTCTTTCCTTTGTTTTTTTGAGAC__AATCTCACTCTGTCACCCAGGCTGAAGTGCA CAG C SKI Ensembl:ENSG00000157933 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1277612506 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_3296987,Human_RBP_ID_11175113 12440 RMVar_ID_12440 Human_SNP_ID_639298 A-to-I Human chr1 - 2363237 2363237 2363237 GCTGTGACACAGTTATTTTCAAGAGATGTAATATACTACTTCATGCGTAAGAACTGTACAATTAT GCTGTGACACAGTTATTTTCAAGAGATGTAATTTACTACTTCATGCGTAAGAACTGTACAATTAT T A MORN1,AL513477.2 Ensembl:ENSG00000116151,Ensembl:ENSG00000272420 Protein coding,lincRNA intron,exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs745790479 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1423371 12441 RMVar_ID_12441 Human_SNP_ID_639299 A-to-I Human chr1 - 2363237 2363237 2363237 GCTGTGACACAGTTATTTTCAAGAGATGTAATATACTACTTCATGCGTAAGAACTGTACAATTAT GCTGTGACACAGTTATTTTCAAGAGATGTAATGTACTACTTCATGCGTAAGAACTGTACAATTAT T C MORN1,AL513477.2 Ensembl:ENSG00000116151,Ensembl:ENSG00000272420 Protein coding,lincRNA intron,exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs745790479 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1423371 12442 RMVar_ID_12442 Human_SNP_ID_639413 A-to-I Human chr1 - 2363724 2363724 2363724 AGGTCTCACTGTCACCCAGGCTGAAGTACAGTAGTGAAATCATAGCTCACTGCAGCCTTGACCTC AGGTCTCACTGTCACCCAGGCTGAAGTACAGTGGTGAAATCATAGCTCACTGCAGCCTTGACCTC T C MORN1 Ensembl:ENSG00000116151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1431567974 Functional Loss SNV dbSNP153 33..33 33 - - - 12443 RMVar_ID_12443 Human_SNP_ID_640228 A-to-I Human chr1 - 2366815 2366815 2366815 ATAGATTTGCCTTGCTGGGTGCAGTGCCTCATACCTGTCATCCTAGCATTTTGAGAGGCTGAGGC ATAGATTTGCCTTGCTGGGTGCAGTGCCTCATTCCTGTCATCCTAGCATTTTGAGAGGCTGAGGC T A MORN1 Ensembl:ENSG00000116151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs535604548 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23371677,Human_RBP_ID_26376633 12444 RMVar_ID_12444 Human_SNP_ID_640510 A-to-I Human chr1 - 2367699 2367699 2367699 TTGCTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCCGAGATCACGCCACTGCACCCCAGAGCAAG TTGCTTGAACCCAGGAGGCAGAGGTTGCAGTGTGCCGAGATCACGCCACTGCACCCCAGAGCAAG T A MORN1 Ensembl:ENSG00000116151 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1160222587 Functional Loss SNV dbSNP153 33..33 33 - - - 12445 RMVar_ID_12445 Human_SNP_ID_640525 A-to-I Human chr1 - 2367766 2367766 2367766 AAAACTAGCTGGGCATAGTGGCGGGTGCCTGTAGTCCCAGCTACTTGAGAGGCTGAGGCAGGGAG AAAACTAGCTGGGCATAGTGGCGGGTGCCTGTTGTCCCAGCTACTTGAGAGGCTGAGGCAGGGAG T A MORN1 Ensembl:ENSG00000116151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1244869580 Functional Loss SNV dbSNP153 33..33 33 - - - 12446 RMVar_ID_12446 Human_SNP_ID_640887 A-to-I Human chr1 - 2369147 2369147 2369147 CAGGGTTTCACCCTGCTAGCCAGGATGATCTCAATCTCCTGACTTCTTGATCCACCACCCTCGGC CAGGGTTTCACCCTGCTAGCCAGGATGATCTCCATCTCCTGACTTCTTGATCCACCACCCTCGGC T G MORN1 Ensembl:ENSG00000116151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223871382 Functional Loss SNV dbSNP153 33..33 33 - - - 12447 RMVar_ID_12447 Human_SNP_ID_652621 A-to-I Human chr1 - 2404498 2404498 2404498 GCGGCCGGGTGGGCAGATGCCGCCGTGGCTCCATCCATCAGCACCCAGTCCTTTGCTTCACTGTG GCGGCCGGGTGGGCAGATGCCGCCGTGGCTCCGTCCATCAGCACCCAGTCCTTTGCTTCACTGTG T C PEX10 Ensembl:ENSG00000157911 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1251460254 Functional Loss SNV dbSNP153 33..33 33 - - - 12448 RMVar_ID_12448 Human_SNP_ID_1087000 A-to-I Human chr1 - 3786306 3786306 3786306 TTTAAAAGAGATGAGGTTTCACCATGTTGGCCAGGTTGGTCTTGAACTCCTGACCTCAAGCAGTC TTTAAAAGAGATGAGGTTTCACCATGTTGGCCCGGTTGGTCTTGAACTCCTGACCTCAAGCAGTC T G LRRC47 Ensembl:ENSG00000130764 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs890693032 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128515,RMVar_hsa_circ_123853,RMVar_hsa_circ_87388,RMVar_hsa_circ_128514,RMVar_hsa_circ_355180,RMVar_hsa_circ_63889 12449 RMVar_ID_12449 Human_SNP_ID_1087019 A-to-I Human chr1 - 3786400 3786400 3786400 CGCCTCCTGGGTTCAAGTGATTCTCCTGCCTCAGCCTGCTGAGTAGCTGGCATTACAGGTGCTCA CGCCTCCTGGGTTCAAGTGATTCTCCTGCCTCGGCCTGCTGAGTAGCTGGCATTACAGGTGCTCA T C LRRC47 Ensembl:ENSG00000130764 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1415483464 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128515,RMVar_hsa_circ_123853,RMVar_hsa_circ_87388,RMVar_hsa_circ_128514,RMVar_hsa_circ_355180,RMVar_hsa_circ_63889 12450 RMVar_ID_12450 Human_SNP_ID_1087022 A-to-I Human chr1 - 3786417 3786417 3786417 AATCTCACTGTAGCGTCCGCCTCCTGGGTTCAAGTGATTCTCCTGCCTCAGCCTGCTGAGTAGCT AATCTCACTGTAGCGTCCGCCTCCTGGGTTCAGGTGATTCTCCTGCCTCAGCCTGCTGAGTAGCT T C LRRC47 Ensembl:ENSG00000130764 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs184477594 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128515,RMVar_hsa_circ_123853,RMVar_hsa_circ_87388,RMVar_hsa_circ_128514,RMVar_hsa_circ_355180,RMVar_hsa_circ_63889 12451 RMVar_ID_12451 Human_SNP_ID_1089634 A-to-I Human chr1 - 3794972 3794972 3794972 TCGGCTCACTTCAACCTCCGCCTCCCGGGTTCAAGCGGTTCTTCTGCCTCAGCCTCCTGAGTAGC TCGGCTCACTTCAACCTCCGCCTCCCGGGTTCGAGCGGTTCTTCTGCCTCAGCCTCCTGAGTAGC T C LRRC47 Ensembl:ENSG00000130764 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs943141396 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123853,RMVar_hsa_circ_128514 12452 RMVar_ID_12452 Human_SNP_ID_1094528 A-to-I Human chr1 - 3812753 3812753 3812753 CCCCTGCAACCTCCGCCTCCCGGGTTCGAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGA CCCCTGCAACCTCCGCCTCCCGGGTTCGAGCATTTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGA T A CEP104 Ensembl:ENSG00000116198 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1245686794 Functional Loss SNV dbSNP153 33..33 33 - - - 12453 RMVar_ID_12453 Human_SNP_ID_1094780 A-to-I Human chr1 - 3813630 3813630 3813630 TGGCCAGGCTGGTCTCGAACTCGTGACCTCATAATCTGCCCACCTTGGCCTCCCAAAGTGCTGGG TGGCCAGGCTGGTCTCGAACTCGTGACCTCATCATCTGCCCACCTTGGCCTCCCAAAGTGCTGGG T G CEP104 Ensembl:ENSG00000116198 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs112926411 Functional Loss SNV dbSNP153 33..33 33 - - - 12454 RMVar_ID_12454 Human_SNP_ID_1108077 A-to-I Human chr1 + 3861541 3861541 3861541 GCTTTCACTTCCTGGGCTCAAGCGATCCTCCTACCTCCGCCCCTGAGTAGCTGGGACTACAGGGG GCTTTCACTTCCTGGGCTCAAGCGATCCTCCTGCCTCCGCCCCTGAGTAGCTGGGACTACAGGGG A G DFFB Ensembl:ENSG00000169598 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1479399502 Functional Loss SNV dbSNP153 33..33 33 - - - 12455 RMVar_ID_12455 Human_SNP_ID_1109302 A-to-I Human chr1 + 3866385 3866385 3866385 TAAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCAAGTGCAACCACGCCCT TAAAGCGATTCTCCTGCCTCAGCCTCCCGAGTGGCTGGGATTACAGGCAAGTGCAACCACGCCCT A G DFFB Ensembl:ENSG00000169598 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs544532020 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123693,RMVar_hsa_circ_294744,RMVar_hsa_circ_128534 12456 RMVar_ID_12456 Human_SNP_ID_1118293 A-to-I Human chr1 - 3898327 3898327 3898327 TTTTGTGTTTTTACTGGAGACAGGTTTTCACCATGTTGGCGAGGCTGGTCTAAAACTCCTGACCT TTTTGTGTTTTTACTGGAGACAGGTTTTCACCGTGTTGGCGAGGCTGGTCTAAAACTCCTGACCT T C C1orf174 Ensembl:ENSG00000198912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs574510389 Functional Loss SNV dbSNP153 33..33 33 - - - 12457 RMVar_ID_12457 Human_SNP_ID_1118298 A-to-I Human chr1 - 3898338 3898338 3898338 GCCCGGCTAATTTTTGTGTTTTTACTGGAGACAGGTTTTCACCATGTTGGCGAGGCTGGTCTAAA GCCCGGCTAATTTTTGTGTTTTTACTGGAGACGGGTTTTCACCATGTTGGCGAGGCTGGTCTAAA T C C1orf174 Ensembl:ENSG00000198912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs986817524 Functional Loss SNV dbSNP153 33..33 33 - - - 12458 RMVar_ID_12458 Human_SNP_ID_1360320 A-to-I Human chr1 + 4780064 4780064 4780064 CACCAGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCTGAGA CACCAGGGAGGCTGAGGCAGGAGAATCGCTTGGACCCAGGAGGCGGAGGTTGCAGTGAGCTGAGA A G AJAP1 Ensembl:ENSG00000196581 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs995839365 Functional Loss SNV dbSNP153 33..33 33 - - - 12459 RMVar_ID_12459 Human_SNP_ID_1706494 A-to-I Human chr1 + 6051965 6051965 6051965 ACCTACTAAAAATACAAAAAATAGCCAGGCATAGTGGGGCGCACCTGTAGTCCCAACTACTCAGG ACCTACTAAAAATACAAAAAATAGCCAGGCATGGTGGGGCGCACCTGTAGTCCCAACTACTCAGG A G KCNAB2 Ensembl:ENSG00000069424 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs775500163 Functional Loss SNV dbSNP153 33..33 33 - - - 12460 RMVar_ID_12460 Human_SNP_ID_1711641 A-to-I Human chr1 - 6072751 6072751 6072751 AGACCCGCAGGCCAGACTTGCCCAGGTTCCTGAAAAACAAACGCCACGTGAGTTCTCAGCACCCA AGACCCGCAGGCCAGACTTGCCCAGGTTCCTGTAAAACAAACGCCACGTGAGTTCTCAGCACCCA T A - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs746414786 Functional Loss SNV dbSNP153 33..33 33 - - - 12461 RMVar_ID_12461 Human_SNP_ID_1745766 A-to-I Human chr1 - 6188479 6188479 6188479 TGCTATGTTGCCTAGGCTGGTCTCGAACTCCTAGATTCAAGGGATCCTCTCACCTTGGCCTCACA TGCTATGTTGCCTAGGCTGGTCTCGAACTCCTGGATTCAAGGGATCCTCTCACCTTGGCCTCACA T C RPL22,AL031847.2 Ensembl:ENSG00000116251,Ensembl:ENSG00000285629 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1197146919 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11062076 RMVar_hsa_circ_128596,RMVar_hsa_circ_120235 12462 RMVar_ID_12462 Human_SNP_ID_1745908 A-to-I Human chr1 - 6188897 6188897 6188897 CCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCTTGAACCCGGGAGACGGAGGTT CCTGTAATCCCAGCTACTCGGGAGGCTGAGGCGGGAGAATTGCTTGAACCCGGGAGACGGAGGTT T C RPL22,AL031847.2 Ensembl:ENSG00000116251,Ensembl:ENSG00000285629 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1462823884 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128596,RMVar_hsa_circ_120235 12463 RMVar_ID_12463 Human_SNP_ID_1746355 A-to-I Human chr1 - 6190448 6190448 6190448 TGAACCAGGGAGGCGGAGGTTGCGGTGAGCCAAGATAGCACCATTGCACTCCAGCCTGGGCAACA TGAACCAGGGAGGCGGAGGTTGCGGTGAGCCATGATAGCACCATTGCACTCCAGCCTGGGCAACA T A RPL22,AL031847.2 Ensembl:ENSG00000116251,Ensembl:ENSG00000285629 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs958055016 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128596,RMVar_hsa_circ_120235 12464 RMVar_ID_12464 Human_SNP_ID_1746390 A-to-I Human chr1 - 6190581 6190581 6190581 TGAGGTCAGGAGTTCTAGACCAGCTGACCAACATGGAGAAACTCCGTTTCTACTAAAAATACAAA TGAGGTCAGGAGTTCTAGACCAGCTGACCAACTTGGAGAAACTCCGTTTCTACTAAAAATACAAA T A RPL22,AL031847.2 Ensembl:ENSG00000116251,Ensembl:ENSG00000285629 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs536923127 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128596,RMVar_hsa_circ_120235 12465 RMVar_ID_12465 Human_SNP_ID_1746797 A-to-I Human chr1 - 6191916 6191916 6191916 TGGCTCACTGCAACCTCTGCCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCTTCCCGAGTTTTT TGGCTCACTGCAACCTCTGCCTCCCAGGTTCACGCGATTCTCCTGCCTCAGCTTCCCGAGTTTTT T G RPL22,AL031847.2 Ensembl:ENSG00000116251,Ensembl:ENSG00000285629 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1275163777 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128596,RMVar_hsa_circ_120235 12466 RMVar_ID_12466 Human_SNP_ID_1746986 A-to-I Human chr1 - 6192613 6192613 6192613 CTCACTGCAGCCTCCGCCTCCTGGGTTCAAGCAGTTGTCCTGCCTCAGCCTCCTGAGTAGCTGAG CTCACTGCAGCCTCCGCCTCCTGGGTTCAAGCGGTTGTCCTGCCTCAGCCTCCTGAGTAGCTGAG T C RPL22,AL031847.2 Ensembl:ENSG00000116251,Ensembl:ENSG00000285629 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1237515857 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128596,RMVar_hsa_circ_120235 12467 RMVar_ID_12467 Human_SNP_ID_1747004 A-to-I Human chr1 - 6192660 6192660 6192660 GAGTCTCACTCCATCGCCCAGGCTGTTGTGCAATGGCGCGATCTCGGCTCACTGCAGCCTCCGCC GAGTCTCACTCCATCGCCCAGGCTGTTGTGCAGTGGCGCGATCTCGGCTCACTGCAGCCTCCGCC T C RPL22,AL031847.2 Ensembl:ENSG00000116251,Ensembl:ENSG00000285629 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1290514689 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11062232,Human_RBP_ID_22557613 RMVar_hsa_circ_128596,RMVar_hsa_circ_120235 12468 RMVar_ID_12468 Human_SNP_ID_1747300 A-to-I Human chr1 - 6193612 6193612 6193612 ACCCCTTCTCTTAAAAATGTTAAGCCAGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGG ACCCCTTCTCTTAAAAATGTTAAGCCAGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG T C RPL22,AL031847.2 Ensembl:ENSG00000116251,Ensembl:ENSG00000285629 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs796319218 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_300295,RMVar_hsa_circ_337176 12469 RMVar_ID_12469 Human_SNP_ID_1748180 A-to-I Human chr1 - 6197168 6197168 6197168 AAAATTAGCTGGGTGTGGTGGTGTGCACCTGTAATCCCAGCTACTCGGGAGGCTGCAGTAGAAGA AAAATTAGCTGGGTGTGGTGGTGTGCACCTGTGATCCCAGCTACTCGGGAGGCTGCAGTAGAAGA T C RPL22,AL031847.2 Ensembl:ENSG00000116251,Ensembl:ENSG00000285629 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1467064553 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_300295,RMVar_hsa_circ_337176 12470 RMVar_ID_12470 Human_SNP_ID_1755186 A-to-I Human chr1 + 6219890 6219890 6219890 CAATCTCTGGCTCACCGCAACCTCCGCCTCCCAGGTTCAAGCGATTCTCCTACCTCAGCCCCCAG CAATCTCTGGCTCACCGCAACCTCCGCCTCCCGGGTTCAAGCGATTCTCCTACCTCAGCCCCCAG A G RNF207 Ensembl:ENSG00000158286 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1452713434 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1413794 12471 RMVar_ID_12471 Human_SNP_ID_1755808 A-to-I Human chr1 - 6222258 6222258 6222258 CCACCATGCCCAGCTAATTTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGATGGCCAGGC CCACCATGCCCAGCTAATTTTTTTGTATTTTTGGTAGAGACGGGGTTTCACCATGATGGCCAGGC T C ICMT Ensembl:ENSG00000116237 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs947538252 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98828,RMVar_hsa_circ_123631,RMVar_hsa_circ_103272,RMVar_hsa_circ_128612,RMVar_hsa_circ_128613,RMVar_hsa_circ_128611 12472 RMVar_ID_12472 Human_SNP_ID_1755815 A-to-I Human chr1 - 6222275 6222275 6222275 GGGATTACAGGCTTGGGCCACCATGCCCAGCTAATTTTTTTGTATTTTTAGTAGAGACGGGGTTT GGGATTACAGGCTTGGGCCACCATGCCCAGCTGATTTTTTTGTATTTTTAGTAGAGACGGGGTTT T C ICMT Ensembl:ENSG00000116237 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1349539942 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98828,RMVar_hsa_circ_123631,RMVar_hsa_circ_103272,RMVar_hsa_circ_128612,RMVar_hsa_circ_128613,RMVar_hsa_circ_128611 12473 RMVar_ID_12473 Human_SNP_ID_1755835 A-to-I Human chr1 - 6222340 6222340 6222340 CGGCTCACCGCAACCTCTGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCT CGGCTCACCGCAACCTCTGCCTCCCGGGTTCAGGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCT T C ICMT Ensembl:ENSG00000116237 Protein coding 3'UTR GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831 HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line - 29129909,29796672,31158229,31158229,32596459 RNA-Seq:(High) rs962810242 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27400342 RMVar_hsa_circ_98828,RMVar_hsa_circ_123631,RMVar_hsa_circ_103272,RMVar_hsa_circ_128612,RMVar_hsa_circ_128613,RMVar_hsa_circ_128611 12474 RMVar_ID_12474 Human_SNP_ID_1755843 A-to-I Human chr1 - 6222360 6222360 6222360 GGAGTGCAGTGGCACCATTTCGGCTCACCGCAACCTCTGCCTCCCGGGTTCAAGCGATTCTCCTG GGAGTGCAGTGGCACCATTTCGGCTCACCGCAGCCTCTGCCTCCCGGGTTCAAGCGATTCTCCTG T C ICMT Ensembl:ENSG00000116237 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs899857779 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18232577,Human_RBP_ID_27400342 RMVar_hsa_circ_98828,RMVar_hsa_circ_123631,RMVar_hsa_circ_103272,RMVar_hsa_circ_128612,RMVar_hsa_circ_128613,RMVar_hsa_circ_128611 12475 RMVar_ID_12475 Human_SNP_ID_1755929 A-to-I Human chr1 - 6222709 6222709 6222709 GCTGTTGGCAGCTGCTGGCCTTGTGGATGGTAAGCTGACTGTGTTGGCATTTAATGCCATCCTCC GCTGTTGGCAGCTGCTGGCCTTGTGGATGGTAGGCTGACTGTGTTGGCATTTAATGCCATCCTCC T C ICMT Ensembl:ENSG00000116237 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1317783625 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_359548,Human_RBP_ID_1433406,Human_RBP_ID_5849331,Human_RBP_ID_8316303,Human_RBP_ID_8750971,Human_RBP_ID_11062635,Human_RBP_ID_17755569,Human_RBP_ID_18232584,Human_RBP_ID_18578948,Human_RBP_ID_26382007 RMVar_hsa_circ_98828,RMVar_hsa_circ_123631,RMVar_hsa_circ_103272,RMVar_hsa_circ_128612,RMVar_hsa_circ_128613,RMVar_hsa_circ_128611 12476 RMVar_ID_12476 Human_SNP_ID_1756085 A-to-I Human chr1 - 6223184 6223184 6223184 AGAATCCTTTGAACCCAGGAGGCGGAGGTTGCAGTGAGTTGAGATCGGGCCTTTGCACTTCAGTC AGAATCCTTTGAACCCAGGAGGCGGAGGTTGCCGTGAGTTGAGATCGGGCCTTTGCACTTCAGTC T G ICMT Ensembl:ENSG00000116237 Protein coding 3'UTR GSE107867;GSE123020:GSM3490832,GSM3490833,GSM3490834 ASD brains,cerebellum;esophageal squamous carcinoma cells,KYSE180 cell line - 30559470,32596459 RNA-Seq:(High) rs1363742300 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98828,RMVar_hsa_circ_123631,RMVar_hsa_circ_103272,RMVar_hsa_circ_128612,RMVar_hsa_circ_128613,RMVar_hsa_circ_128611 12477 RMVar_ID_12477 Human_SNP_ID_1756095 A-to-I Human chr1 - 6223236 6223236 6223236 GGGCGTGCTGGCGGGTGCCTGTAATCCCAGCTACTCAGGAGGCTGAGACAGGAGAATCCTTTGAA GGGCGTGCTGGCGGGTGCCTGTAATCCCAGCTCCTCAGGAGGCTGAGACAGGAGAATCCTTTGAA T G ICMT Ensembl:ENSG00000116237 Protein coding 3'UTR GSE100210;GSE99789;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,29796672,32596459 RNA-Seq:(High) rs1282788286 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98828,RMVar_hsa_circ_123631,RMVar_hsa_circ_103272,RMVar_hsa_circ_128612,RMVar_hsa_circ_128613,RMVar_hsa_circ_128611 12478 RMVar_ID_12478 Human_SNP_ID_1756097 A-to-I Human chr1 - 6223246 6223246 6223246 AAAAATAGCTGGGCGTGCTGGCGGGTGCCTGTAATCCCAGCTACTCAGGAGGCTGAGACAGGAGA AAAAATAGCTGGGCGTGCTGGCGGGTGCCTGTGATCCCAGCTACTCAGGAGGCTGAGACAGGAGA T C ICMT Ensembl:ENSG00000116237 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1351949600 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98828,RMVar_hsa_circ_123631,RMVar_hsa_circ_103272,RMVar_hsa_circ_128612,RMVar_hsa_circ_128613,RMVar_hsa_circ_128611 12479 RMVar_ID_12479 Human_SNP_ID_1756118 A-to-I Human chr1 - 6223305 6223305 6223305 CAGGCGTTCGAGACCAGCCTGGCCAACATGATAAAACCCCGTCTCTACTAAAAATACAAAAAAAT CAGGCGTTCGAGACCAGCCTGGCCAACATGATGAAACCCCGTCTCTACTAAAAATACAAAAAAAT T C ICMT Ensembl:ENSG00000116237 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1346470430 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2709455 RMVar_hsa_circ_98828,RMVar_hsa_circ_123631,RMVar_hsa_circ_103272,RMVar_hsa_circ_128612,RMVar_hsa_circ_128613,RMVar_hsa_circ_128611 12480 RMVar_ID_12480 Human_SNP_ID_1756161 A-to-I Human chr1 - 6223380 6223380 6223380 ACAGACGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCAATTTGGGAGGCCAAGGCGGGTGG ACAGACGGCCGGGCGCGGTGGCTCACGCCTGTGATCCCAGCAATTTGGGAGGCCAAGGCGGGTGG T C ICMT Ensembl:ENSG00000116237 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1322257769 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2084748 RMVar_hsa_circ_98828,RMVar_hsa_circ_123631,RMVar_hsa_circ_103272,RMVar_hsa_circ_128612,RMVar_hsa_circ_128613,RMVar_hsa_circ_128611 12481 RMVar_ID_12481 Human_SNP_ID_1759991 A-to-I Human chr1 + 6236294 6236294 6236294 GAAACGAGCCGAGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCTGGCGA GAAACGAGCCGAGCGCGGTGGCTCACGCCTGTTATCCCAGCACTTTGGGAGGCCGAGGCTGGCGA A T LINC00337 Ensembl:ENSG00000225077 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1178298700 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_11789 12482 RMVar_ID_12482 Human_SNP_ID_1764733 A-to-I Human chr1 - 6251893 6251893 6251893 ACTTTGGGAGGCCGAGGCAGGAGGATCTCTTAAGCCCAGGAGATGGAGGCTGCAGTGAGCCATGA ACTTTGGGAGGCCGAGGCAGGAGGATCTCTTAGGCCCAGGAGATGGAGGCTGCAGTGAGCCATGA T C GPR153 Ensembl:ENSG00000158292 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1044684753 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98596,RMVar_hsa_circ_108023,RMVar_hsa_circ_128621,RMVar_hsa_circ_128622 12483 RMVar_ID_12483 Human_SNP_ID_1824046 A-to-I Human chr1 - 6464041 6464041 6464041 TTAAAACTTGGGCTGAAGGAGGTTGAGGCTGCAGTGAGCTATGATCGTGCCACTGCACTTCAGCC TTAAAACTTGGGCTGAAGGAGGTTGAGGCTGCGGTGAGCTATGATCGTGCCACTGCACTTCAGCC T C TNFRSF25 Ensembl:ENSG00000215788 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs564358391 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11072130 12484 RMVar_ID_12484 Human_SNP_ID_1829654 A-to-I Human chr1 - 6479794 6479794 6479794 CTAGCCTGGGCAACATAGTGAGATCTGTCACTACTAAAAATAAAAAAGTTAGTTGGGCGTAGTGG CTAGCCTGGGCAACATAGTGAGATCTGTCACTGCTAAAAATAAAAAAGTTAGTTGGGCGTAGTGG T C PLEKHG5 Ensembl:ENSG00000171680 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1331040759 Functional Loss SNV dbSNP153 33..33 33 - - - 12485 RMVar_ID_12485 Human_SNP_ID_1840812 A-to-I Human chr1 - 6522101 6522100 6522102 GACCTCGTGATCCGTCCACCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCC GACCTCGTGATCCGTCCACCTTGGCCTCCCA__GTGCTGGGATTACAGGCGTGAGCCACCGCGCC CTT C NOL9 Ensembl:ENSG00000162408 Protein coding 3'UTR GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1165436278 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_360369,Human_RBP_ID_11218935 RMVar_hsa_circ_99109,RMVar_hsa_circ_122804,RMVar_hsa_circ_119236,RMVar_hsa_circ_128644,RMVar_hsa_circ_85958,RMVar_hsa_circ_91784,RMVar_hsa_circ_128646,RMVar_hsa_circ_81527,RMVar_hsa_circ_128647,RMVar_hsa_circ_128645,RMVar_hsa_circ_128642,RMVar_hsa_circ_128643 12486 RMVar_ID_12486 Human_SNP_ID_1840812 A-to-I Human chr1 - 6522102 6522100 6522102 TGACCTCGTGATCCGTCCACCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGC TGACCTCGTGATCCGTCCACCTTGGCCTCCCA__GTGCTGGGATTACAGGCGTGAGCCACCGCGC CTT C NOL9 Ensembl:ENSG00000162408 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1165436278 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_360369,Human_RBP_ID_11218935 RMVar_hsa_circ_99109,RMVar_hsa_circ_122804,RMVar_hsa_circ_119236,RMVar_hsa_circ_128644,RMVar_hsa_circ_85958,RMVar_hsa_circ_91784,RMVar_hsa_circ_128646,RMVar_hsa_circ_81527,RMVar_hsa_circ_128647,RMVar_hsa_circ_128645,RMVar_hsa_circ_128642,RMVar_hsa_circ_128643 12487 RMVar_ID_12487 Human_SNP_ID_1840813 A-to-I Human chr1 - 6522102 6522102 6522102 TGACCTCGTGATCCGTCCACCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGC TGACCTCGTGATCCGTCCACCTTGGCCTCCCAGAGTGCTGGGATTACAGGCGTGAGCCACCGCGC T C NOL9 Ensembl:ENSG00000162408 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1367818293 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_360369,Human_RBP_ID_11218935 RMVar_hsa_circ_99109,RMVar_hsa_circ_122804,RMVar_hsa_circ_119236,RMVar_hsa_circ_128644,RMVar_hsa_circ_85958,RMVar_hsa_circ_91784,RMVar_hsa_circ_128646,RMVar_hsa_circ_81527,RMVar_hsa_circ_128647,RMVar_hsa_circ_128645,RMVar_hsa_circ_128642,RMVar_hsa_circ_128643 12488 RMVar_ID_12488 Human_SNP_ID_1840832 A-to-I Human chr1 - 6522161 6522161 6522161 TTTTGTATTTTTAGTAGAGATGGGGTTTTACTATGTTGGCTAGGCTGGTCTCGAGCTCCTGACCT TTTTGTATTTTTAGTAGAGATGGGGTTTTACTTTGTTGGCTAGGCTGGTCTCGAGCTCCTGACCT T A NOL9 Ensembl:ENSG00000162408 Protein coding 3'UTR GSE100210;GSE99789;GSE107867 HepG2 cell line;esophageal squamous carcinoma cells,EC109;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 29129909,29796672,30559470 RNA-Seq:(High) rs1243171033 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4063132,Human_RBP_ID_11076137,Human_RBP_ID_22369365 RMVar_hsa_circ_99109,RMVar_hsa_circ_122804,RMVar_hsa_circ_119236,RMVar_hsa_circ_128644,RMVar_hsa_circ_85958,RMVar_hsa_circ_91784,RMVar_hsa_circ_128646,RMVar_hsa_circ_81527,RMVar_hsa_circ_128647,RMVar_hsa_circ_128645,RMVar_hsa_circ_128642,RMVar_hsa_circ_128643 12489 RMVar_ID_12489 Human_SNP_ID_1840845 A-to-I Human chr1 - 6522198 6522198 6522198 GGGATTACAGGCGCCCGCCACTACACTAGCTAATTTTTTTTGTATTTTTAGTAGAGATGGGGTTT GGGATTACAGGCGCCCGCCACTACACTAGCTATTTTTTTTTGTATTTTTAGTAGAGATGGGGTTT T A NOL9 Ensembl:ENSG00000162408 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs988264944 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_98194,Human_RBP_ID_5853782,Human_RBP_ID_21879636 RMVar_hsa_circ_99109,RMVar_hsa_circ_122804,RMVar_hsa_circ_119236,RMVar_hsa_circ_128644,RMVar_hsa_circ_85958,RMVar_hsa_circ_91784,RMVar_hsa_circ_128646,RMVar_hsa_circ_81527,RMVar_hsa_circ_128647,RMVar_hsa_circ_128645,RMVar_hsa_circ_128642,RMVar_hsa_circ_128643 12490 RMVar_ID_12490 Human_SNP_ID_1840846 A-to-I Human chr1 - 6522198 6522198 6522198 GGGATTACAGGCGCCCGCCACTACACTAGCTAATTTTTTTTGTATTTTTAGTAGAGATGGGGTTT GGGATTACAGGCGCCCGCCACTACACTAGCTAGTTTTTTTTGTATTTTTAGTAGAGATGGGGTTT T C NOL9 Ensembl:ENSG00000162408 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs988264944 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_98194,Human_RBP_ID_5853782,Human_RBP_ID_21879636 RMVar_hsa_circ_99109,RMVar_hsa_circ_122804,RMVar_hsa_circ_119236,RMVar_hsa_circ_128644,RMVar_hsa_circ_85958,RMVar_hsa_circ_91784,RMVar_hsa_circ_128646,RMVar_hsa_circ_81527,RMVar_hsa_circ_128647,RMVar_hsa_circ_128645,RMVar_hsa_circ_128642,RMVar_hsa_circ_128643 12491 RMVar_ID_12491 Human_SNP_ID_1840891 A-to-I Human chr1 - 6522365 6522365 6522365 TTGTATTTTTAGTAGAGATGGCGTTTCACTTTATTGGTCAGGCTGGTCTCGAACTTCCAACCTCA TTGTATTTTTAGTAGAGATGGCGTTTCACTTTGTTGGTCAGGCTGGTCTCGAACTTCCAACCTCA T C NOL9 Ensembl:ENSG00000162408 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1446751588 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5853793,Human_RBP_ID_11076142,Human_RBP_ID_18232975,Human_RBP_ID_23150412,Human_RBP_ID_26382230 Human_miRNA_ID_52828,Human_miRNA_ID_60406,Human_miRNA_ID_559668,Human_miRNA_ID_2061872,Human_miRNA_ID_2899541 RMVar_hsa_circ_99109,RMVar_hsa_circ_122804,RMVar_hsa_circ_119236,RMVar_hsa_circ_128644,RMVar_hsa_circ_85958,RMVar_hsa_circ_91784,RMVar_hsa_circ_128646,RMVar_hsa_circ_81527,RMVar_hsa_circ_128647,RMVar_hsa_circ_128645,RMVar_hsa_circ_128642,RMVar_hsa_circ_128643 12492 RMVar_ID_12492 Human_SNP_ID_1840903 A-to-I Human chr1 - 6522387 6522387 6522387 TGCCACCACACCCAGCTAATTTTTGTATTTTTAGTAGAGATGGCGTTTCACTTTATTGGTCAGGC TGCCACCACACCCAGCTAATTTTTGTATTTTTGGTAGAGATGGCGTTTCACTTTATTGGTCAGGC T C NOL9 Ensembl:ENSG00000162408 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs983007241 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11076142 Human_miRNA_ID_52828,Human_miRNA_ID_60406,Human_miRNA_ID_559668 RMVar_hsa_circ_99109,RMVar_hsa_circ_122804,RMVar_hsa_circ_119236,RMVar_hsa_circ_128644,RMVar_hsa_circ_85958,RMVar_hsa_circ_91784,RMVar_hsa_circ_128646,RMVar_hsa_circ_81527,RMVar_hsa_circ_128647,RMVar_hsa_circ_128645,RMVar_hsa_circ_128642,RMVar_hsa_circ_128643 12493 RMVar_ID_12493 Human_SNP_ID_1840933 A-to-I Human chr1 - 6522498 6522498 6522498 TCGCCAAGGCTGGAGTGCAGTGGCCTGATCTCAGGTCACTGCAACCTCTGCCTCCTGGGTTCAAG TCGCCAAGGCTGGAGTGCAGTGGCCTGATCTCGGGTCACTGCAACCTCTGCCTCCTGGGTTCAAG T C NOL9 Ensembl:ENSG00000162408 Protein coding 3'UTR GSE38233;GSE100210;GSE99789;GSE107867 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;ASD brains,temporal_cortex - 24183664,29129909,29796672,30559470 RNA-Seq:(High) rs1299007709 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_605585,Human_miRNA_ID_2270906 RMVar_hsa_circ_99109,RMVar_hsa_circ_122804,RMVar_hsa_circ_119236,RMVar_hsa_circ_128644,RMVar_hsa_circ_85958,RMVar_hsa_circ_91784,RMVar_hsa_circ_128646,RMVar_hsa_circ_81527,RMVar_hsa_circ_128647,RMVar_hsa_circ_128645,RMVar_hsa_circ_128642,RMVar_hsa_circ_128643 12494 RMVar_ID_12494 Human_SNP_ID_1840980 A-to-I Human chr1 - 6522629 6522629 6522629 CGCCCGCCTTGGCCTCCGAAAGTGCTGGGATTACAGGCGTGAGCCACTGCGCCTGGCCTGAAGCT CGCCCGCCTTGGCCTCCGAAAGTGCTGGGATTCCAGGCGTGAGCCACTGCGCCTGGCCTGAAGCT T G NOL9 Ensembl:ENSG00000162408 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs958164008 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26382235 RMVar_hsa_circ_99109,RMVar_hsa_circ_122804,RMVar_hsa_circ_119236,RMVar_hsa_circ_128644,RMVar_hsa_circ_85958,RMVar_hsa_circ_91784,RMVar_hsa_circ_128646,RMVar_hsa_circ_81527,RMVar_hsa_circ_128647,RMVar_hsa_circ_128645,RMVar_hsa_circ_128642,RMVar_hsa_circ_128643 12495 RMVar_ID_12495 Human_SNP_ID_1840981 A-to-I Human chr1 - 6522641 6522640 6522641 GACCTCGTGATCCGCCCGCCTTGGCCTCCGAAAGTGCTGGGATTACAGGCGTGAGCCACTGCGCC GACCTCGTGATCCGCCCGCCTTGGCCTCCGAA_GTGCTGGGATTACAGGCGTGAGCCACTGCGCC CT C NOL9 Ensembl:ENSG00000162408 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs920613011 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_99109,RMVar_hsa_circ_122804,RMVar_hsa_circ_119236,RMVar_hsa_circ_128644,RMVar_hsa_circ_85958,RMVar_hsa_circ_91784,RMVar_hsa_circ_128646,RMVar_hsa_circ_81527,RMVar_hsa_circ_128647,RMVar_hsa_circ_128645,RMVar_hsa_circ_128642,RMVar_hsa_circ_128643 12496 RMVar_ID_12496 Human_SNP_ID_1841224 A-to-I Human chr1 - 6523317 6523317 6523317 CCTTGGCCTCCCAAAGTGTTGGGATTACAGGCATGAGCCACCGCACCCGGCTGGTGGCAGTGGCT CCTTGGCCTCCCAAAGTGTTGGGATTACAGGCGTGAGCCACCGCACCCGGCTGGTGGCAGTGGCT T C NOL9 Ensembl:ENSG00000162408 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1045458153 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_360377,Human_RBP_ID_4063152,Human_RBP_ID_11076192 RMVar_hsa_circ_99109,RMVar_hsa_circ_122804,RMVar_hsa_circ_119236,RMVar_hsa_circ_128644,RMVar_hsa_circ_85958,RMVar_hsa_circ_91784,RMVar_hsa_circ_128646,RMVar_hsa_circ_81527,RMVar_hsa_circ_128647,RMVar_hsa_circ_128645,RMVar_hsa_circ_128642,RMVar_hsa_circ_128643 12497 RMVar_ID_12497 Human_SNP_ID_1841243 A-to-I Human chr1 - 6523397 6523397 6523397 TTTTCTATTTTTAGTAGAGAAGGGGTTTCACCATGTTGGCCAGGCTGGTTTTGAACTCCTGTCCT TTTTCTATTTTTAGTAGAGAAGGGGTTTCACCGTGTTGGCCAGGCTGGTTTTGAACTCCTGTCCT T C NOL9 Ensembl:ENSG00000162408 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs534439053 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4063156 RMVar_hsa_circ_99109,RMVar_hsa_circ_122804,RMVar_hsa_circ_119236,RMVar_hsa_circ_128644,RMVar_hsa_circ_85958,RMVar_hsa_circ_91784,RMVar_hsa_circ_128646,RMVar_hsa_circ_81527,RMVar_hsa_circ_128647,RMVar_hsa_circ_128645,RMVar_hsa_circ_128642,RMVar_hsa_circ_128643 12498 RMVar_ID_12498 Human_SNP_ID_1841268 A-to-I Human chr1 - 6523533 6523533 6523533 CTCTTGTTGCCCAGGCTGGAGTGCAGTGGCGCAATCTGGGCTCACTGCCACCTCCGCCTCCCGGG CTCTTGTTGCCCAGGCTGGAGTGCAGTGGCGCGATCTGGGCTCACTGCCACCTCCGCCTCCCGGG T C NOL9 Ensembl:ENSG00000162408 Protein coding 3'UTR GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1211757704 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4063158 RMVar_hsa_circ_99109,RMVar_hsa_circ_122804,RMVar_hsa_circ_119236,RMVar_hsa_circ_128644,RMVar_hsa_circ_85958,RMVar_hsa_circ_91784,RMVar_hsa_circ_128646,RMVar_hsa_circ_81527,RMVar_hsa_circ_128647,RMVar_hsa_circ_128645,RMVar_hsa_circ_128642,RMVar_hsa_circ_128643 12499 RMVar_ID_12499 Human_SNP_ID_1841701 A-to-I Human chr1 - 6525034 6525022 6525035 AATTTCTTTCAAATCTGGAAAACCTCGGGGCCAGGCGCAGTGGCTCACGCCTGTAATTCCAGCAC AATTTCTTTCAAATCTGGAAAACCTCGGGGC_____________TCACGCCTGTAATTCCAGCAC AGCCACTGCGCCTG A NOL9 Ensembl:ENSG00000162408 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285806843 Functional Loss DEL dbSNP153 32..44 33 - - - RMVar_hsa_circ_99109,RMVar_hsa_circ_122804,RMVar_hsa_circ_119236,RMVar_hsa_circ_128644,RMVar_hsa_circ_85958,RMVar_hsa_circ_91784,RMVar_hsa_circ_128646,RMVar_hsa_circ_81527,RMVar_hsa_circ_128647,RMVar_hsa_circ_128645,RMVar_hsa_circ_128642,RMVar_hsa_circ_128643 12500 RMVar_ID_12500 Human_SNP_ID_1841704 A-to-I Human chr1 - 6525028 6525028 6525028 TTTCAAATCTGGAAAACCTCGGGGCCAGGCGCAGTGGCTCACGCCTGTAATTCCAGCACTTTGGG TTTCAAATCTGGAAAACCTCGGGGCCAGGCGCGGTGGCTCACGCCTGTAATTCCAGCACTTTGGG T C NOL9 Ensembl:ENSG00000162408 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1276604282 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99109,RMVar_hsa_circ_122804,RMVar_hsa_circ_119236,RMVar_hsa_circ_128644,RMVar_hsa_circ_85958,RMVar_hsa_circ_91784,RMVar_hsa_circ_128646,RMVar_hsa_circ_81527,RMVar_hsa_circ_128647,RMVar_hsa_circ_128645,RMVar_hsa_circ_128642,RMVar_hsa_circ_128643 12501 RMVar_ID_12501 Human_SNP_ID_1842946 A-to-I Human chr1 - 6529421 6529421 6529421 ACCATGCCTGGCTAATTTTGTGTTTTTTGTAGAGACAAGGTTTCACCACGTTGGTCAGGCTGGTC ACCATGCCTGGCTAATTTTGTGTTTTTTGTAGGGACAAGGTTTCACCACGTTGGTCAGGCTGGTC T C NOL9 Ensembl:ENSG00000162408 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1396232190 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5854025,Human_RBP_ID_11076577 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 12502 RMVar_ID_12502 Human_SNP_ID_1844965 A-to-I Human chr1 - 6536760 6536760 6536760 CAGGCTGGAGTACAGTGGCGTAATCACAGCTCACTGCATCCTCCACCTTCTGAGCTCAGGCTAGC CAGGCTGGAGTACAGTGGCGTAATCACAGCTCGCTGCATCCTCCACCTTCTGAGCTCAGGCTAGC T C NOL9 Ensembl:ENSG00000162408 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs993910304 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82584,RMVar_hsa_circ_122804,RMVar_hsa_circ_119236,RMVar_hsa_circ_91784,RMVar_hsa_circ_128646,RMVar_hsa_circ_128647,RMVar_hsa_circ_128645,RMVar_hsa_circ_9386,RMVar_hsa_circ_128649,RMVar_hsa_circ_65372,RMVar_hsa_circ_79485,RMVar_hsa_circ_272524,RMVar_hsa_circ_339515,RMVar_hsa_circ_128648,RMVar_hsa_circ_370006,RMVar_hsa_circ_128654,RMVar_hsa_circ_128655,RMVar_hsa_circ_128653,RMVar_hsa_circ_128657,RMVar_hsa_circ_378388,RMVar_hsa_circ_271146,RMVar_hsa_circ_277292,RMVar_hsa_circ_289399,RMVar_hsa_circ_128659,RMVar_hsa_circ_128660 12503 RMVar_ID_12503 Human_SNP_ID_1846253 A-to-I Human chr1 - 6541461 6541461 6541461 TACTGTTAATCAGGCTGCCTGTGGTGGCTCACACTTGTAATCCCAGCACTTGGGGAGGCTGAGGC TACTGTTAATCAGGCTGCCTGTGGTGGCTCACTCTTGTAATCCCAGCACTTGGGGAGGCTGAGGC T A NOL9 Ensembl:ENSG00000162408 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs908986112 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5156380 RMVar_hsa_circ_82584,RMVar_hsa_circ_122804,RMVar_hsa_circ_119236,RMVar_hsa_circ_91784,RMVar_hsa_circ_128646,RMVar_hsa_circ_128647,RMVar_hsa_circ_128645,RMVar_hsa_circ_9386,RMVar_hsa_circ_128649,RMVar_hsa_circ_65372,RMVar_hsa_circ_79485,RMVar_hsa_circ_272524,RMVar_hsa_circ_339515,RMVar_hsa_circ_128648,RMVar_hsa_circ_370006,RMVar_hsa_circ_128654,RMVar_hsa_circ_128655,RMVar_hsa_circ_128653,RMVar_hsa_circ_128657,RMVar_hsa_circ_378388,RMVar_hsa_circ_271146,RMVar_hsa_circ_277292,RMVar_hsa_circ_289399,RMVar_hsa_circ_128659,RMVar_hsa_circ_128660,RMVar_hsa_circ_128661 12504 RMVar_ID_12504 Human_SNP_ID_1846687 A-to-I Human chr1 - 6543010 6543010 6543010 ATGTGCCTGTGGTCCCAGCTACTTGGGAGGCTAAGGAGGGAGTATTGCTTGAGCCCAGGAGGTCG ATGTGCCTGTGGTCCCAGCTACTTGGGAGGCTGAGGAGGGAGTATTGCTTGAGCCCAGGAGGTCG T C NOL9 Ensembl:ENSG00000162408 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs978827971 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17556505 RMVar_hsa_circ_82584,RMVar_hsa_circ_119236,RMVar_hsa_circ_91784,RMVar_hsa_circ_128646,RMVar_hsa_circ_128647,RMVar_hsa_circ_9386,RMVar_hsa_circ_128649,RMVar_hsa_circ_79485,RMVar_hsa_circ_339515,RMVar_hsa_circ_128648,RMVar_hsa_circ_370006,RMVar_hsa_circ_128654,RMVar_hsa_circ_128655,RMVar_hsa_circ_378388,RMVar_hsa_circ_289399,RMVar_hsa_circ_128662,RMVar_hsa_circ_309121,RMVar_hsa_circ_128660,RMVar_hsa_circ_342850,RMVar_hsa_circ_52106,RMVar_hsa_circ_297903,RMVar_hsa_circ_128663,RMVar_hsa_circ_128664 12505 RMVar_ID_12505 Human_SNP_ID_1846959 A-to-I Human chr1 - 6543875 6543875 6543875 GTTATCTGCCCGCCTTAGCCTCCCAAAGTGCTAGGATTACAGGCGTGAGCCACCATGCCCGGCCT GTTATCTGCCCGCCTTAGCCTCCCAAAGTGCTTGGATTACAGGCGTGAGCCACCATGCCCGGCCT T A NOL9 Ensembl:ENSG00000162408 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1190884467 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82584,RMVar_hsa_circ_119236,RMVar_hsa_circ_91784,RMVar_hsa_circ_128646,RMVar_hsa_circ_128647,RMVar_hsa_circ_9386,RMVar_hsa_circ_128649,RMVar_hsa_circ_79485,RMVar_hsa_circ_339515,RMVar_hsa_circ_128648,RMVar_hsa_circ_370006,RMVar_hsa_circ_128654,RMVar_hsa_circ_128655,RMVar_hsa_circ_378388,RMVar_hsa_circ_289399,RMVar_hsa_circ_128662,RMVar_hsa_circ_309121,RMVar_hsa_circ_128660,RMVar_hsa_circ_342850,RMVar_hsa_circ_52106,RMVar_hsa_circ_297903,RMVar_hsa_circ_128663,RMVar_hsa_circ_128664 12506 RMVar_ID_12506 Human_SNP_ID_1848010 A-to-I Human chr1 - 6547683 6547682 6547684 TCCCGGCTAATTTTTGTAGTTTTTGTAGAGATAGGATTTTGCCATGTTGCCCAGGCTGGTCACGA TCCCGGCTAATTTTTGTAGTTTTTGTAGAGA__GGATTTTGCCATGTTGCCCAGGCTGGTCACGA CTA C NOL9 Ensembl:ENSG00000162408 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1444985961 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_11077207 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 12507 RMVar_ID_12507 Human_SNP_ID_1848014 A-to-I Human chr1 - 6547689 6547689 6547689 CATGACTCCCGGCTAATTTTTGTAGTTTTTGTAGAGATAGGATTTTGCCATGTTGCCCAGGCTGG CATGACTCCCGGCTAATTTTTGTAGTTTTTGTGGAGATAGGATTTTGCCATGTTGCCCAGGCTGG T C NOL9 Ensembl:ENSG00000162408 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs961466986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11077207 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 12508 RMVar_ID_12508 Human_SNP_ID_1848213 A-to-I Human chr1 - 6548179 6548179 6548179 TGCGCCACTGCACACTCCAGCCTGGGAGACAGAGTGAGAATCCGTCTCAAAAAAAAAAAAAAAAA TGCGCCACTGCACACTCCAGCCTGGGAGACAGTGTGAGAATCCGTCTCAAAAAAAAAAAAAAAAA T A NOL9 Ensembl:ENSG00000162408 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1325485093 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24721025 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 12509 RMVar_ID_12509 Human_SNP_ID_1859012 A-to-I Human chr1 + 6584166 6584166 6584166 TCAAACTCCTGACCTTGCGATCCACCTGCCTTAGCTTCCCAAAGTGCTGGGATTACAGGCGAGAG TCAAACTCCTGACCTTGCGATCCACCTGCCTTGGCTTCCCAAAGTGCTGGGATTACAGGCGAGAG A G ZBTB48 Ensembl:ENSG00000204859 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1450908159 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11077466 12510 RMVar_ID_12510 Human_SNP_ID_1865324 A-to-I Human chr1 - 6602760 6602757 6602761 TGCTTCCCTTCTCGGACCCCGCGCACGCCCTGAGCCTGCTGCGCGGCCTGAGCCAGCTGCGCGCC TGCTTCCCTTCTCGGACCCCGCGCACGCCCT____CTGCTGCGCGGCCTGAGCCAGCTGCGCGCC GGCTC G KLHL21 Ensembl:ENSG00000162413 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1438800252 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_4072475,Human_RBP_ID_8754622,Human_RBP_ID_9252585,Human_RBP_ID_9269587,Human_RBP_ID_9319687,Human_RBP_ID_27400639 12511 RMVar_ID_12511 Human_SNP_ID_1866175 A-to-I Human chr1 - 6605527 6605527 6605527 GGTTCAAGCTTGAAGTGTTTGAACCTGGAGGCAGAGGTTGCAGTGAGCTCAGATCGTGCCAGTGC GGTTCAAGCTTGAAGTGTTTGAACCTGGAGGCCGAGGTTGCAGTGAGCTCAGATCGTGCCAGTGC T G KLHL21 Ensembl:ENSG00000162413 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1488394064 Functional Loss SNV dbSNP153 33..33 33 - - - 12512 RMVar_ID_12512 Human_SNP_ID_1866559 A-to-I Human chr1 - 6606973 6606973 6606973 AGGTGTTGTGGTGCGTGCCTGTGATCCTAGCTACTCGAGAGGCTGAGGCAGGAGAATCACTGGAA AGGTGTTGTGGTGCGTGCCTGTGATCCTAGCTTCTCGAGAGGCTGAGGCAGGAGAATCACTGGAA T A KLHL21 Ensembl:ENSG00000162413 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs536789780 Functional Loss SNV dbSNP153 33..33 33 - - - 12513 RMVar_ID_12513 Human_SNP_ID_1874643 A-to-I Human chr1 + 6631237 6631237 6631237 GGGGGTCTTGCTATCTTGCCCAGTCTGGTCTCAAACTCTTGGATTCAGGGGATTCTCCTGCCTTG GGGGGTCTTGCTATCTTGCCCAGTCTGGTCTCGAACTCTTGGATTCAGGGGATTCTCCTGCCTTG A G THAP3 Ensembl:ENSG00000041988 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs996076714 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17556892 12514 RMVar_ID_12514 Human_SNP_ID_1877365 A-to-I Human chr1 - 6639462 6639462 6639462 AGCCGGGCGTGGTGGCACGTGCCTGTAATCCCAGCTACCTGGGAGGCTGAGACAGGAGAATTGCT AGCCGGGCGTGGTGGCACGTGCCTGTAATCCCCGCTACCTGGGAGGCTGAGACAGGAGAATTGCT T G DNAJC11 Ensembl:ENSG00000007923 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1406622160 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3677,RMVar_hsa_circ_71082 12515 RMVar_ID_12515 Human_SNP_ID_1877366 A-to-I Human chr1 - 6639468 6639468 6639468 AAAATTAGCCGGGCGTGGTGGCACGTGCCTGTAATCCCAGCTACCTGGGAGGCTGAGACAGGAGA AAAATTAGCCGGGCGTGGTGGCACGTGCCTGTGATCCCAGCTACCTGGGAGGCTGAGACAGGAGA T C DNAJC11 Ensembl:ENSG00000007923 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1451461580 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3677,RMVar_hsa_circ_71082 12516 RMVar_ID_12516 Human_SNP_ID_1879540 A-to-I Human chr1 - 6646921 6646921 6646921 TGAACTCCTGGGGTGAAGCAATTTGCCTCCTCAGCCTCCCAAAGTGCTGGGGTTACAGGTGTGAG TGAACTCCTGGGGTGAAGCAATTTGCCTCCTCGGCCTCCCAAAGTGCTGGGGTTACAGGTGTGAG T C DNAJC11 Ensembl:ENSG00000007923 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs956435676 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5125124,Human_RBP_ID_11078161,Human_RBP_ID_22469147,Human_RBP_ID_23150478 RMVar_hsa_circ_71082,RMVar_hsa_circ_26219 12517 RMVar_ID_12517 Human_SNP_ID_1879646 A-to-I Human chr1 - 6647246 6647246 6647246 AAACCCCATCTCTACTAAAAATACAAAATATTAACCGGACATGGTGGTGGGCGCCTGTAGTCCCA AAACCCCATCTCTACTAAAAATACAAAATATTTACCGGACATGGTGGTGGGCGCCTGTAGTCCCA T A DNAJC11 Ensembl:ENSG00000007923 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1246610731 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71082,RMVar_hsa_circ_26219 12518 RMVar_ID_12518 Human_SNP_ID_1879650 A-to-I Human chr1 - 6647276 6647276 6647276 GAATTCGAGACCAGTCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAATATTAAC GAATTCGAGACCAGTCTGGCCAACATGGTGAACCCCCATCTCTACTAAAAATACAAAATATTAAC T G DNAJC11 Ensembl:ENSG00000007923 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs139493199 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71082,RMVar_hsa_circ_26219 12519 RMVar_ID_12519 Human_SNP_ID_1879664 A-to-I Human chr1 - 6647356 6647356 6647356 CCTGTTGGCTGGGCACAGTGGCTCGTGCCTATAATCCCAGCACTTTGGGAGGCTGAGGCAGGTGG CCTGTTGGCTGGGCACAGTGGCTCGTGCCTATGATCCCAGCACTTTGGGAGGCTGAGGCAGGTGG T C DNAJC11 Ensembl:ENSG00000007923 Protein coding intron GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs908885019 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71082,RMVar_hsa_circ_26219 12520 RMVar_ID_12520 Human_SNP_ID_1879736 A-to-I Human chr1 - 6647652 6647652 6647652 CACCACGCCTAGCTAATTTTTGTATTTTTACTAGAGACGGGGTTTCACCATGTTGGCCAGGATGG CACCACGCCTAGCTAATTTTTGTATTTTTACTGGAGACGGGGTTTCACCATGTTGGCCAGGATGG T C DNAJC11 Ensembl:ENSG00000007923 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs904199531 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71082,RMVar_hsa_circ_26219 12521 RMVar_ID_12521 Human_SNP_ID_1879757 A-to-I Human chr1 - 6647739 6647739 6647739 GCAGTCTTGGCTCACTGCAACCTCCACCTCCCAGGTTCAAGCTATTCTGCCTCAGCCTCCCAAGT GCAGTCTTGGCTCACTGCAACCTCCACCTCCCGGGTTCAAGCTATTCTGCCTCAGCCTCCCAAGT T C DNAJC11 Ensembl:ENSG00000007923 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs60327053 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71082,RMVar_hsa_circ_26219 12522 RMVar_ID_12522 Human_SNP_ID_1879932 A-to-I Human chr1 - 6648422 6648422 6648422 GTCAGGTGCGGTGGCTCATGCCTGTAATCCCAACACTTTGGGAGGCCAAGGCAGGCGGGTCGCCT GTCAGGTGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGCGGGTCGCCT T C DNAJC11 Ensembl:ENSG00000007923 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs368131706 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71082,RMVar_hsa_circ_26219 12523 RMVar_ID_12523 Human_SNP_ID_1879989 A-to-I Human chr1 - 6648665 6648665 6648665 ATCACTTGAGCTCAGGAGTTTGAGACCAGCCTAGGCAACATGGCAAAACCTTGACTCTACAAAAA ATCACTTGAGCTCAGGAGTTTGAGACCAGCCTGGGCAACATGGCAAAACCTTGACTCTACAAAAA T C DNAJC11 Ensembl:ENSG00000007923 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs985061936 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71082,RMVar_hsa_circ_26219 12524 RMVar_ID_12524 Human_SNP_ID_1880082 A-to-I Human chr1 - 6649068 6649068 6649068 GGATTGCTTGAACCCGGGAGGTTGAGGCTGCAATGAGCTGAGATTGCACCACTGTACCCCAGCCT GGATTGCTTGAACCCGGGAGGTTGAGGCTGCAGTGAGCTGAGATTGCACCACTGTACCCCAGCCT T C DNAJC11 Ensembl:ENSG00000007923 Protein coding intron GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line - 24183664,31158229 RNA-Seq:(High) rs962846714 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557575 RMVar_hsa_circ_71082,RMVar_hsa_circ_26219 12525 RMVar_ID_12525 Human_SNP_ID_1880095 A-to-I Human chr1 - 6649130 6649130 6649130 AGGAAAAGGAGCCGATGTGACTCACACCTGCAATCCCAGGGCTTTGGGAGGCCAAGGTGGGAGGA AGGAAAAGGAGCCGATGTGACTCACACCTGCAGTCCCAGGGCTTTGGGAGGCCAAGGTGGGAGGA T C DNAJC11 Ensembl:ENSG00000007923 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1322286981 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2161433 RMVar_hsa_circ_71082,RMVar_hsa_circ_26219 12526 RMVar_ID_12526 Human_SNP_ID_1880200 A-to-I Human chr1 - 6649433 6649433 6649433 TGAGCACGGTGGCTCATGCCTCTAATCCCAGCACTTTAGGAGGCCGAGGCGGGTGGATCACGAGA TGAGCACGGTGGCTCATGCCTCTAATCCCAGCCCTTTAGGAGGCCGAGGCGGGTGGATCACGAGA T G DNAJC11 Ensembl:ENSG00000007923 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs190019361 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71082,RMVar_hsa_circ_26219 12527 RMVar_ID_12527 Human_SNP_ID_1880204 A-to-I Human chr1 - 6649441 6649440 6649442 TTCCTGGCTGAGCACGGTGGCTCATGCCTCTAATCCCAGCACTTTAGGAGGCCGAGGCGGGTGGA TTCCTGGCTGAGCACGGTGGCTCATGCCTCT__TCCCAGCACTTTAGGAGGCCGAGGCGGGTGGA ATT A DNAJC11 Ensembl:ENSG00000007923 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1190237904 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_71082,RMVar_hsa_circ_26219 12528 RMVar_ID_12528 Human_SNP_ID_1880320 A-to-I Human chr1 - 6649868 6649868 6649868 AACCCCCTCTACTAAAAATATAAAAATTAACCAGGCATGGTGGCGCTTGCCTGTAGTCCCAGCTA AACCCCCTCTACTAAAAATATAAAAATTAACCGGGCATGGTGGCGCTTGCCTGTAGTCCCAGCTA T C DNAJC11 Ensembl:ENSG00000007923 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1429256674 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11078239,Human_RBP_ID_17756511 RMVar_hsa_circ_71082,RMVar_hsa_circ_26219 12529 RMVar_ID_12529 Human_SNP_ID_1880389 A-to-I Human chr1 - 6650154 6650154 6650154 GGCTCAGGTGACCCTCCTGAGTAGCTGGGACTACAGGTGTGCACCACCATGCCTGACTAATTTTT GGCTCAGGTGACCCTCCTGAGTAGCTGGGACTGCAGGTGTGCACCACCATGCCTGACTAATTTTT T C DNAJC11 Ensembl:ENSG00000007923 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs561150123 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71082,RMVar_hsa_circ_26219 12530 RMVar_ID_12530 Human_SNP_ID_1880419 A-to-I Human chr1 - 6650318 6650318 6650318 CAAGCAGTCCTCCCACCTTGGCCTCCCAAAGCACTGAGATTAGAAGCATGAGCCACTTCAGCAAG CAAGCAGTCCTCCCACCTTGGCCTCCCAAAGCCCTGAGATTAGAAGCATGAGCCACTTCAGCAAG T G DNAJC11 Ensembl:ENSG00000007923 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1307115166 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11078252 RMVar_hsa_circ_71082,RMVar_hsa_circ_26219 12531 RMVar_ID_12531 Human_SNP_ID_1880443 A-to-I Human chr1 - 6650444 6650444 6650444 CTCCTCCCTCAGCCTCCCGAAAAACTAGGACTACAGGCGTGTGCCAACATGCCTGGCTCATTGTT CTCCTCCCTCAGCCTCCCGAAAAACTAGGACTGCAGGCGTGTGCCAACATGCCTGGCTCATTGTT T C DNAJC11 Ensembl:ENSG00000007923 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1024430003 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11078263,Human_RBP_ID_23150504,Human_RBP_ID_24721270 RMVar_hsa_circ_71082,RMVar_hsa_circ_26219 12532 RMVar_ID_12532 Human_SNP_ID_1880444 A-to-I Human chr1 - 6650450 6650450 6650450 GCAGTCCTCCTCCCTCAGCCTCCCGAAAAACTAGGACTACAGGCGTGTGCCAACATGCCTGGCTC GCAGTCCTCCTCCCTCAGCCTCCCGAAAAACTGGGACTACAGGCGTGTGCCAACATGCCTGGCTC T C DNAJC11 Ensembl:ENSG00000007923 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs964152201 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11078263,Human_RBP_ID_22488654,Human_RBP_ID_23150504,Human_RBP_ID_24721270 RMVar_hsa_circ_71082,RMVar_hsa_circ_26219 12533 RMVar_ID_12533 Human_SNP_ID_1880515 A-to-I Human chr1 - 6650790 6650790 6650790 CGGCTCACTGCAGCCTCTGCCTCCTGGGTTCAAGCTATTCTCCTGTCTCAACCTTCCGAGTAGCT CGGCTCACTGCAGCCTCTGCCTCCTGGGTTCAGGCTATTCTCCTGTCTCAACCTTCCGAGTAGCT T C DNAJC11 Ensembl:ENSG00000007923 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1288210724 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71082,RMVar_hsa_circ_26219 12534 RMVar_ID_12534 Human_SNP_ID_1921060 A-to-I Human chr1 + 6803746 6803746 6803746 AAATTATTTTATTTCTTTTTAAAGATGGTCTCACTCTGTCATCCAGGCTGGAGTGCAGAGGTGTG AAATTATTTTATTTCTTTTTAAAGATGGTCTCGCTCTGTCATCCAGGCTGGAGTGCAGAGGTGTG A G CAMTA1 Ensembl:ENSG00000171735 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1450695090 Functional Loss SNV dbSNP153 33..33 33 - - - 12535 RMVar_ID_12535 Human_SNP_ID_1921061 A-to-I Human chr1 + 6803746 6803746 6803746 AAATTATTTTATTTCTTTTTAAAGATGGTCTCACTCTGTCATCCAGGCTGGAGTGCAGAGGTGTG AAATTATTTTATTTCTTTTTAAAGATGGTCTCTCTCTGTCATCCAGGCTGGAGTGCAGAGGTGTG A T CAMTA1 Ensembl:ENSG00000171735 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1450695090 Functional Loss SNV dbSNP153 33..33 33 - - - 12536 RMVar_ID_12536 Human_SNP_ID_1931452 A-to-I Human chr1 + 6847133 6847133 6847133 TCAAGCTGTTCTTTTGCCTCAGCCTACCGAGTAGCTGGGATTATAGGCTTGTGCCACTGCGCCTG TCAAGCTGTTCTTTTGCCTCAGCCTACCGAGTGGCTGGGATTATAGGCTTGTGCCACTGCGCCTG A G CAMTA1 Ensembl:ENSG00000171735 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1199316048 Functional Loss SNV dbSNP153 33..33 33 - - - 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 12537 RMVar_ID_12537 Human_SNP_ID_2171116 A-to-I Human chr1 + 7797541 7797541 7797541 CCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCAGCTTGCACCCAGGAGGTGGAGGT CCTGTAATCCCAGCTACTCGGGAGGCTGAGGCGGGAGAATCAGCTTGCACCCAGGAGGTGGAGGT A G PER3 Ensembl:ENSG00000049246 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1484948842 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 12538 RMVar_ID_12538 Human_SNP_ID_2203532 A-to-I Human chr1 - 7918277 7918277 7918277 TGTGTTAAAAAATATCTTCTTTGTGGCCAGGCACGGTAGCTCACACCTGTAATCCCAGCACTTTG TGTGTTAAAAAATATCTTCTTTGTGGCCAGGCCCGGTAGCTCACACCTGTAATCCCAGCACTTTG T G TNFRSF9 Ensembl:ENSG00000049249 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs953310510 Functional Loss SNV dbSNP153 33..33 33 - - - 12539 RMVar_ID_12539 Human_SNP_ID_2203561 A-to-I Human chr1 - 7918433 7918433 7918433 CAGAGGTTGCAGTGAGCTGGGACCGCATCACTACACTTCAGCCTGGGCAACAGAGAAAAACCTTT CAGAGGTTGCAGTGAGCTGGGACCGCATCACTTCACTTCAGCCTGGGCAACAGAGAAAAACCTTT T A TNFRSF9 Ensembl:ENSG00000049249 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs918888748 Functional Loss SNV dbSNP153 33..33 33 - - - 12540 RMVar_ID_12540 Human_SNP_ID_2203562 A-to-I Human chr1 - 7918433 7918433 7918433 CAGAGGTTGCAGTGAGCTGGGACCGCATCACTACACTTCAGCCTGGGCAACAGAGAAAAACCTTT CAGAGGTTGCAGTGAGCTGGGACCGCATCACTGCACTTCAGCCTGGGCAACAGAGAAAAACCTTT T C TNFRSF9 Ensembl:ENSG00000049249 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs918888748 Functional Loss SNV dbSNP153 33..33 33 - - - 12541 RMVar_ID_12541 Human_SNP_ID_2203841 A-to-I Human chr1 - 7919605 7919605 7919605 AAACTCCTGGGCTCAAGTGATCCACCCGCCTCAGTCTCCCAAGTAGCTGGGATTACAGGTGCAAA AAACTCCTGGGCTCAAGTGATCCACCCGCCTCGGTCTCCCAAGTAGCTGGGATTACAGGTGCAAA T C TNFRSF9 Ensembl:ENSG00000049249 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs956268670 Functional Loss SNV dbSNP153 33..33 33 - - - 12542 RMVar_ID_12542 Human_SNP_ID_2204016 A-to-I Human chr1 - 7920395 7920395 7920395 CTTTGGCCTCCCAAAGTGCTGGGATTACAGACATGAACTGCCAGGCCCGGCCAAAATAATGCACC CTTTGGCCTCCCAAAGTGCTGGGATTACAGACGTGAACTGCCAGGCCCGGCCAAAATAATGCACC T C TNFRSF9 Ensembl:ENSG00000049249 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs927244725 Functional Loss SNV dbSNP153 33..33 33 - - - 12543 RMVar_ID_12543 Human_SNP_ID_2216892 A-to-I Human chr1 + 7968615 7968615 7968615 TCAGCTCACTGCAGCCTCTGCCTCCTAGGTTCAAGCGATTCTCCTGCCTCAACCCCCCAAGTAGA TCAGCTCACTGCAGCCTCTGCCTCCTAGGTTCGAGCGATTCTCCTGCCTCAACCCCCCAAGTAGA A G PARK7 Ensembl:ENSG00000116288 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1367896021 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15853,RMVar_hsa_circ_122172,RMVar_hsa_circ_364026,RMVar_hsa_circ_128706,RMVar_hsa_circ_92240,RMVar_hsa_circ_128707,RMVar_hsa_circ_320129 12544 RMVar_ID_12544 Human_SNP_ID_2217375 A-to-I Human chr1 + 7969936 7969936 7969936 ATGGAGGTCAGGTGCAGTGGCTCAACGTCTATAATCCCAGTGGTTTGGGAGGCTGAGACAGGAGG ATGGAGGTCAGGTGCAGTGGCTCAACGTCTATGATCCCAGTGGTTTGGGAGGCTGAGACAGGAGG A G PARK7 Ensembl:ENSG00000116288 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1481752291 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15853,RMVar_hsa_circ_122172,RMVar_hsa_circ_364026,RMVar_hsa_circ_128706,RMVar_hsa_circ_92240,RMVar_hsa_circ_128707,RMVar_hsa_circ_320129,RMVar_hsa_circ_15848,RMVar_hsa_circ_76820,RMVar_hsa_circ_128708 12545 RMVar_ID_12545 Human_SNP_ID_2217415 A-to-I Human chr1 + 7970048 7970048 7970048 ACGCCATCTCTACAAAAAATTTTCTTTTAATTAGCTGGGCACGGTGGTGCACACTTGTAGTCCCA ACGCCATCTCTACAAAAAATTTTCTTTTAATTGGCTGGGCACGGTGGTGCACACTTGTAGTCCCA A G PARK7 Ensembl:ENSG00000116288 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1040433973 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15853,RMVar_hsa_circ_122172,RMVar_hsa_circ_364026,RMVar_hsa_circ_128706,RMVar_hsa_circ_92240,RMVar_hsa_circ_128707,RMVar_hsa_circ_320129,RMVar_hsa_circ_15848,RMVar_hsa_circ_76820,RMVar_hsa_circ_128708 12546 RMVar_ID_12546 Human_SNP_ID_2218178 A-to-I Human chr1 + 7972757 7972757 7972757 GAAATCCCGTTTCTACTAAAAATACAAAAGTTAGCTGGGCATGGTGGTGCACGCCTGTAATCCCA GAAATCCCGTTTCTACTAAAAATACAAAAGTTGGCTGGGCATGGTGGTGCACGCCTGTAATCCCA A G PARK7 Ensembl:ENSG00000116288 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1188296256 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15853,RMVar_hsa_circ_122172,RMVar_hsa_circ_128706,RMVar_hsa_circ_92240,RMVar_hsa_circ_128707,RMVar_hsa_circ_99617,RMVar_hsa_circ_15848,RMVar_hsa_circ_76820,RMVar_hsa_circ_128708,RMVar_hsa_circ_128709 12547 RMVar_ID_12547 Human_SNP_ID_2218903 A-to-I Human chr1 + 7975077 7975077 7975077 GGGGTTTCACCATGTTAGCCAGGCTGGTCTCGAACTCCTGATCTCGTGATCCGCCCACCTTGGCC GGGGTTTCACCATGTTAGCCAGGCTGGTCTCGGACTCCTGATCTCGTGATCCGCCCACCTTGGCC A G PARK7 Ensembl:ENSG00000116288 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1557447840 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15853,RMVar_hsa_circ_122172,RMVar_hsa_circ_128706,RMVar_hsa_circ_92240,RMVar_hsa_circ_128707,RMVar_hsa_circ_99617,RMVar_hsa_circ_15848,RMVar_hsa_circ_76820,RMVar_hsa_circ_128708,RMVar_hsa_circ_128709 12548 RMVar_ID_12548 Human_SNP_ID_2218916 A-to-I Human chr1 + 7975122 7975122 7975122 GTGATCCGCCCACCTTGGCCTCCCAAAGTGCTAGGATTACAGGCGTGAGCCACCGCACCCAGCCA GTGATCCGCCCACCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCACCCAGCCA A G PARK7 Ensembl:ENSG00000116288 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1458303028 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15853,RMVar_hsa_circ_122172,RMVar_hsa_circ_128706,RMVar_hsa_circ_92240,RMVar_hsa_circ_128707,RMVar_hsa_circ_99617,RMVar_hsa_circ_15848,RMVar_hsa_circ_76820,RMVar_hsa_circ_128708,RMVar_hsa_circ_128709 12549 RMVar_ID_12549 Human_SNP_ID_2220117 A-to-I Human chr1 + 7979640 7979640 7979640 CTCTCACCTCAGCCTCCCGAGTAGCTGGAACTATGGGTATGAGCCACCACACTTGGCTAATTTTT CTCTCACCTCAGCCTCCCGAGTAGCTGGAACTGTGGGTATGAGCCACCACACTTGGCTAATTTTT A G PARK7 Ensembl:ENSG00000116288 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1437604139 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122172,RMVar_hsa_circ_128706,RMVar_hsa_circ_92240,RMVar_hsa_circ_128707,RMVar_hsa_circ_99617,RMVar_hsa_circ_76820,RMVar_hsa_circ_128708,RMVar_hsa_circ_377066,RMVar_hsa_circ_128709,RMVar_hsa_circ_128710 12550 RMVar_ID_12550 Human_SNP_ID_2220146 A-to-I Human chr1 + 7979762 7979761 7979762 GGCCTCAAGCGATCCTTCTGGCTTGGCCTCCCAAAGTACTAGGATTACAGATGTGAGCCACTGTG GGCCTCAAGCGATCCTTCTGGCTTGGCCTCCC_AAGTACTAGGATTACAGATGTGAGCCACTGTG CA C PARK7 Ensembl:ENSG00000116288 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs796747224 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_122172,RMVar_hsa_circ_128706,RMVar_hsa_circ_92240,RMVar_hsa_circ_128707,RMVar_hsa_circ_99617,RMVar_hsa_circ_76820,RMVar_hsa_circ_128708,RMVar_hsa_circ_377066,RMVar_hsa_circ_128709,RMVar_hsa_circ_128710 12551 RMVar_ID_12551 Human_SNP_ID_2334313 A-to-I Human chr1 - 8403968 8403968 8403968 AAATTAGCTGGACGTGGTGACGCGTGCCTGTAATCCCAGCTACTCAGGTGGCTAAGGCAGGAGAA AAATTAGCTGGACGTGGTGACGCGTGCCTGTAGTCCCAGCTACTCAGGTGGCTAAGGCAGGAGAA T C RERE Ensembl:ENSG00000142599 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1490786745 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128715,RMVar_hsa_circ_114520,RMVar_hsa_circ_61106,RMVar_hsa_circ_335312,RMVar_hsa_circ_59089 12552 RMVar_ID_12552 Human_SNP_ID_2336607 A-to-I Human chr1 - 8412939 8412939 8412939 AAGGAAAAAAAAATCCATCAACAGTCATAGGAAGCTTACAAAGCTTCGGAGATCTGGCACCACCA AAGGAAAAAAAAATCCATCAACAGTCATAGGAGGCTTACAAAGCTTCGGAGATCTGGCACCACCA T C RERE Ensembl:ENSG00000142599 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1557618921 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128715,RMVar_hsa_circ_114520,RMVar_hsa_circ_61106,RMVar_hsa_circ_335312,RMVar_hsa_circ_59089 12553 RMVar_ID_12553 Human_SNP_ID_2336609 A-to-I Human chr1 - 8412943 8412943 8412943 ACCAAAGGAAAAAAAAATCCATCAACAGTCATAGGAAGCTTACAAAGCTTCGGAGATCTGGCACC ACCAAAGGAAAAAAAAATCCATCAACAGTCATGGGAAGCTTACAAAGCTTCGGAGATCTGGCACC T C RERE Ensembl:ENSG00000142599 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs933601251 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128715,RMVar_hsa_circ_114520,RMVar_hsa_circ_61106,RMVar_hsa_circ_335312,RMVar_hsa_circ_59089 12554 RMVar_ID_12554 Human_SNP_ID_2336785 A-to-I Human chr1 - 8413552 8413552 8413552 ATCACTTGAGCCCAGGAGTTCAAGTCTAGCCTAGGCAACATGGTGAAACCCCATCTCTACAAAAA ATCACTTGAGCCCAGGAGTTCAAGTCTAGCCTTGGCAACATGGTGAAACCCCATCTCTACAAAAA T A RERE Ensembl:ENSG00000142599 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1418150896 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128715,RMVar_hsa_circ_114520,RMVar_hsa_circ_61106,RMVar_hsa_circ_335312,RMVar_hsa_circ_59089 12555 RMVar_ID_12555 Human_SNP_ID_2380147 A-to-I Human chr1 - 8582299 8582299 8582299 GGGAGGCTGAGGCGGTAGGATTGCTTGAACCCAGGAGTTTAAGGCTATTGTGTGCTGTGATCAGC GGGAGGCTGAGGCGGTAGGATTGCTTGAACCCCGGAGTTTAAGGCTATTGTGTGCTGTGATCAGC T G RERE Ensembl:ENSG00000142599 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335562337 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24769888 RMVar_hsa_circ_8704,RMVar_hsa_circ_52274,RMVar_hsa_circ_59089,RMVar_hsa_circ_296079,RMVar_hsa_circ_62912,RMVar_hsa_circ_337011,RMVar_hsa_circ_296431,RMVar_hsa_circ_281245,RMVar_hsa_circ_274528,RMVar_hsa_circ_309733,RMVar_hsa_circ_349230,RMVar_hsa_circ_49926,RMVar_hsa_circ_305891,RMVar_hsa_circ_128733,RMVar_hsa_circ_101600,RMVar_hsa_circ_277627,RMVar_hsa_circ_313286,RMVar_hsa_circ_291989,RMVar_hsa_circ_293781,RMVar_hsa_circ_128731,RMVar_hsa_circ_128726,RMVar_hsa_circ_285877,RMVar_hsa_circ_270631,RMVar_hsa_circ_42946,RMVar_hsa_circ_128735,RMVar_hsa_circ_128734,RMVar_hsa_circ_128742,RMVar_hsa_circ_128744,RMVar_hsa_circ_273130,RMVar_hsa_circ_308785,RMVar_hsa_circ_128732,RMVar_hsa_circ_276769,RMVar_hsa_circ_128743,RMVar_hsa_circ_128745,RMVar_hsa_circ_77022 12556 RMVar_ID_12556 Human_SNP_ID_2382570 A-to-I Human chr1 - 8592664 8592664 8592664 TTTCCCAGGCTAGTCTTGAATTCCTGGCCACAAGCATTCTTCTCACTTAGGCCTCCCAAAGTGCT TTTCCCAGGCTAGTCTTGAATTCCTGGCCACAGGCATTCTTCTCACTTAGGCCTCCCAAAGTGCT T C RERE Ensembl:ENSG00000142599 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1248084683 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8704,RMVar_hsa_circ_52274,RMVar_hsa_circ_59089,RMVar_hsa_circ_296079,RMVar_hsa_circ_62912,RMVar_hsa_circ_337011,RMVar_hsa_circ_296431,RMVar_hsa_circ_281245,RMVar_hsa_circ_274528,RMVar_hsa_circ_309733,RMVar_hsa_circ_349230,RMVar_hsa_circ_49926,RMVar_hsa_circ_305891,RMVar_hsa_circ_128733,RMVar_hsa_circ_101600,RMVar_hsa_circ_277627,RMVar_hsa_circ_313286,RMVar_hsa_circ_291989,RMVar_hsa_circ_293781,RMVar_hsa_circ_128731,RMVar_hsa_circ_128726,RMVar_hsa_circ_285877,RMVar_hsa_circ_270631,RMVar_hsa_circ_42946,RMVar_hsa_circ_128734,RMVar_hsa_circ_128742,RMVar_hsa_circ_128744,RMVar_hsa_circ_273130,RMVar_hsa_circ_308785,RMVar_hsa_circ_128732,RMVar_hsa_circ_276769,RMVar_hsa_circ_128743,RMVar_hsa_circ_128745,RMVar_hsa_circ_77022 12557 RMVar_ID_12557 Human_SNP_ID_2386018 A-to-I Human chr1 - 8605421 8605421 8605421 ACCTCTTAAAGTAAGTTGGGAAGGCCAGGCTCAGTGGCTCACATCTGTAATCCCAGCACTTTGGG ACCTCTTAAAGTAAGTTGGGAAGGCCAGGCTCGGTGGCTCACATCTGTAATCCCAGCACTTTGGG T C RERE Ensembl:ENSG00000142599 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1336481171 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17556913 RMVar_hsa_circ_8704,RMVar_hsa_circ_52274,RMVar_hsa_circ_59089,RMVar_hsa_circ_296079,RMVar_hsa_circ_62912,RMVar_hsa_circ_337011,RMVar_hsa_circ_296431,RMVar_hsa_circ_281245,RMVar_hsa_circ_274528,RMVar_hsa_circ_309733,RMVar_hsa_circ_349230,RMVar_hsa_circ_49926,RMVar_hsa_circ_305891,RMVar_hsa_circ_128733,RMVar_hsa_circ_101600,RMVar_hsa_circ_277627,RMVar_hsa_circ_313286,RMVar_hsa_circ_291989,RMVar_hsa_circ_293781,RMVar_hsa_circ_128731,RMVar_hsa_circ_128726,RMVar_hsa_circ_285877,RMVar_hsa_circ_270631,RMVar_hsa_circ_42946,RMVar_hsa_circ_128734,RMVar_hsa_circ_128742,RMVar_hsa_circ_128744,RMVar_hsa_circ_273130,RMVar_hsa_circ_308785,RMVar_hsa_circ_128732,RMVar_hsa_circ_276769,RMVar_hsa_circ_128743,RMVar_hsa_circ_128745,RMVar_hsa_circ_77022 12558 RMVar_ID_12558 Human_SNP_ID_2386888 A-to-I Human chr1 - 8608164 8608164 8608164 ATCTGAACAGCTGGGTGTGGTGGCTCATGCCTATAATCCCAGCACCTTGGGAGGCTGAGGAGAGA ATCTGAACAGCTGGGTGTGGTGGCTCATGCCTGTAATCCCAGCACCTTGGGAGGCTGAGGAGAGA T C RERE Ensembl:ENSG00000142599 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1316368192 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8704,RMVar_hsa_circ_52274,RMVar_hsa_circ_59089,RMVar_hsa_circ_296079,RMVar_hsa_circ_62912,RMVar_hsa_circ_337011,RMVar_hsa_circ_296431,RMVar_hsa_circ_281245,RMVar_hsa_circ_274528,RMVar_hsa_circ_309733,RMVar_hsa_circ_349230,RMVar_hsa_circ_49926,RMVar_hsa_circ_305891,RMVar_hsa_circ_128733,RMVar_hsa_circ_101600,RMVar_hsa_circ_277627,RMVar_hsa_circ_313286,RMVar_hsa_circ_291989,RMVar_hsa_circ_293781,RMVar_hsa_circ_128731,RMVar_hsa_circ_128726,RMVar_hsa_circ_285877,RMVar_hsa_circ_270631,RMVar_hsa_circ_42946,RMVar_hsa_circ_128734,RMVar_hsa_circ_128742,RMVar_hsa_circ_128744,RMVar_hsa_circ_273130,RMVar_hsa_circ_308785,RMVar_hsa_circ_128732,RMVar_hsa_circ_276769,RMVar_hsa_circ_128743,RMVar_hsa_circ_128745,RMVar_hsa_circ_77022 12559 RMVar_ID_12559 Human_SNP_ID_2397477 A-to-I Human chr1 - 8651908 8651908 8651908 GAGAGTCTCAGGTGGGAGGATCACTTGAGGCCAGGAGTTTAAGGCTGCAGTGAACTACATGCCAT GAGAGTCTCAGGTGGGAGGATCACTTGAGGCCGGGAGTTTAAGGCTGCAGTGAACTACATGCCAT T C RERE Ensembl:ENSG00000142599 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348155441 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 12560 RMVar_ID_12560 Human_SNP_ID_2413231 A-to-I Human chr1 - 8715144 8715144 8715144 TTGTGGGCTGGGCGTGGTGGCTCACGACTGTAATCCCGGCACTTTGGGAGGCCAGGACGGGCAGA TTGTGGGCTGGGCGTGGTGGCTCACGACTGTATTCCCGGCACTTTGGGAGGCCAGGACGGGCAGA T A RERE Ensembl:ENSG00000142599 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs367616650 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22469942 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 12561 RMVar_ID_12561 Human_SNP_ID_2415590 A-to-I Human chr1 - 8725522 8725522 8725522 TCACTCTGTTGCTCAGGCTGGAGTGCAGTGGCACGATGTCGGCTTACTGCAACCTCTGCCTCCCG TCACTCTGTTGCTCAGGCTGGAGTGCAGTGGCGCGATGTCGGCTTACTGCAACCTCTGCCTCCCG T C RERE Ensembl:ENSG00000142599 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1162271320 Functional Loss SNV dbSNP153 33..33 33 - - - 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 12562 RMVar_ID_12562 Human_SNP_ID_2416549 A-to-I Human chr1 - 8729095 8729095 8729095 GTGTGGCACGATCTCAGCTCACCGCAGCTTCCACCTCCCGGGTTCAAACGATTCTCTGCCTCAGC GTGTGGCACGATCTCAGCTCACCGCAGCTTCCTCCTCCCGGGTTCAAACGATTCTCTGCCTCAGC T A RERE Ensembl:ENSG00000142599 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1157374785 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24734318 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 12563 RMVar_ID_12563 Human_SNP_ID_2416550 A-to-I Human chr1 - 8729095 8729095 8729095 GTGTGGCACGATCTCAGCTCACCGCAGCTTCCACCTCCCGGGTTCAAACGATTCTCTGCCTCAGC GTGTGGCACGATCTCAGCTCACCGCAGCTTCCGCCTCCCGGGTTCAAACGATTCTCTGCCTCAGC T C RERE Ensembl:ENSG00000142599 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1157374785 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24734318 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 12564 RMVar_ID_12564 Human_SNP_ID_2417939 A-to-I Human chr1 - 8734021 8734021 8734021 CTGACTGCAACCTCCACCTCTGGGTTCAAGCAATTCTCCTGCATCAGCCTCCCGAGTAGAGTAGC CTGACTGCAACCTCCACCTCTGGGTTCAAGCAGTTCTCCTGCATCAGCCTCCCGAGTAGAGTAGC T C RERE Ensembl:ENSG00000142599 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs533060950 Functional Loss SNV dbSNP153 33..33 33 - - - 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 12565 RMVar_ID_12565 Human_SNP_ID_2424319 A-to-I Human chr1 - 8760209 8760209 8760209 CAGTCTGGCCAACATGATGAAACCCCGTCTCTACTGAAAATACAAAAAATTAGCTGGGCGCGGTG CAGTCTGGCCAACATGATGAAACCCCGTCTCTCCTGAAAATACAAAAAATTAGCTGGGCGCGGTG T G RERE Ensembl:ENSG00000142599 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1297360022 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24734462 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 12566 RMVar_ID_12566 Human_SNP_ID_2427949 A-to-I Human chr1 - 8774546 8774546 8774546 AGTTCAAGACCAGCCTGACACAACATGGAGAAACCCTGCCTCTACTAAAAATACAAAATTAGCCG AGTTCAAGACCAGCCTGACACAACATGGAGAACCCCTGCCTCTACTAAAAATACAAAATTAGCCG T G RERE Ensembl:ENSG00000142599 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1043180756 Functional Loss SNV dbSNP153 33..33 33 - - - 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 12567 RMVar_ID_12567 Human_SNP_ID_2433272 A-to-I Human chr1 - 8795303 8795303 8795303 AAAAAAGTGGGGGGCCGGGGGCGGTGGCTTACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGC AAAAAAGTGGGGGGCCGGGGGCGGTGGCTTACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGC T C RERE Ensembl:ENSG00000142599 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256907517 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101600,RMVar_hsa_circ_128732 12568 RMVar_ID_12568 Human_SNP_ID_2434704 A-to-I Human chr1 - 8800709 8800709 8800709 CACACGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTCTGAGCCACCACTTCTGGCCCTTACAA CACACGCCTCGGCCTCCCAAAGTGCTGGGATTGCAGGTCTGAGCCACCACTTCTGGCCCTTACAA T C RERE Ensembl:ENSG00000142599 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs539679357 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101600,RMVar_hsa_circ_128732 12569 RMVar_ID_12569 Human_SNP_ID_2435907 A-to-I Human chr1 - 8805328 8805328 8805328 TTGTATTTTTAGTAGAGATGGGGTTTCACCATATTGGCTAGGTTGTTCTGGAACTCTTGACCTCA TTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCTAGGTTGTTCTGGAACTCTTGACCTCA T C RERE Ensembl:ENSG00000142599 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1319291024 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11135917,Human_RBP_ID_17556926,Human_RBP_ID_22469950 RMVar_hsa_circ_101600,RMVar_hsa_circ_128732 12570 RMVar_ID_12570 Human_SNP_ID_2452756 A-to-I Human chr1 - 8868834 8868834 8868834 ATCTCTATAAAAAAAAAATATAAAAATTAGCCAGGCATGATGGTGCATGCCTATAGTCCCAGCTG ATCTCTATAAAAAAAAAATATAAAAATTAGCCGGGCATGATGGTGCATGCCTATAGTCCCAGCTG T C ENO1 Ensembl:ENSG00000074800 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs774404755 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35208,RMVar_hsa_circ_119925,RMVar_hsa_circ_120513,RMVar_hsa_circ_117677,RMVar_hsa_circ_128755,RMVar_hsa_circ_96254,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_95596,RMVar_hsa_circ_112436,RMVar_hsa_circ_81853,RMVar_hsa_circ_128783,RMVar_hsa_circ_128785,RMVar_hsa_circ_128786,RMVar_hsa_circ_128784,RMVar_hsa_circ_103334,RMVar_hsa_circ_265042,RMVar_hsa_circ_128788 12571 RMVar_ID_12571 Human_SNP_ID_2453809 A-to-I Human chr1 - 8872438 8872437 8872439 GTGGAGATTGCAGTGAGCCAAGATCACGCCATACACTCTAGCCTGGGGGATAGAGCGAGATTCTG GTGGAGATTGCAGTGAGCCAAGATCACGCCA__CACTCTAGCCTGGGGGATAGAGCGAGATTCTG GTA G ENO1 Ensembl:ENSG00000074800 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1377267066 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_9546640,Human_RBP_ID_24770274 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_128791,RMVar_hsa_circ_128792 12572 RMVar_ID_12572 Human_SNP_ID_2455322 A-to-I Human chr1 - 8877664 8877664 8877664 TTTAGTAGAGGCGGTGTTTCACCATGTTGGCCAGGCTGGTCTTGAGCTCCCGACCTCAGGTGATC TTTAGTAGAGGCGGTGTTTCACCATGTTGGCCTGGCTGGTCTTGAGCTCCCGACCTCAGGTGATC T A ENO1 Ensembl:ENSG00000074800 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1326051655 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11140515,Human_RBP_ID_23150775 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 12573 RMVar_ID_12573 Human_SNP_ID_2504359 A-to-I Human chr1 - 9056254 9056254 9056254 TTGAGCCTGGGAAGCGGAGGTTGCCGTGAGCTAAGATCGCACCATCGCACTCCAGCCTGGGCAAC TTGAGCCTGGGAAGCGGAGGTTGCCGTGAGCTGAGATCGCACCATCGCACTCCAGCCTGGGCAAC T C SLC2A5 Ensembl:ENSG00000142583 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs994195045 Functional Loss SNV dbSNP153 33..33 33 - - - 12574 RMVar_ID_12574 Human_SNP_ID_2516056 A-to-I Human chr1 - 9100904 9100904 9100904 GCCTCCACCTCCCAGGCTCAAGCGATCCTCCCACCTCAGCTCCCTGAGAAGCTGGGACCACAGGC GCCTCCACCTCCCAGGCTCAAGCGATCCTCCCGCCTCAGCTCCCTGAGAAGCTGGGACCACAGGC T C GPR157 Ensembl:ENSG00000180758 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1465930780 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5156405 12575 RMVar_ID_12575 Human_SNP_ID_2516061 A-to-I Human chr1 - 9100923 9100923 9100923 GCAATCATGGCTCACTGCAGCCTCCACCTCCCAGGCTCAAGCGATCCTCCCACCTCAGCTCCCTG GCAATCATGGCTCACTGCAGCCTCCACCTCCCGGGCTCAAGCGATCCTCCCACCTCAGCTCCCTG T C GPR157 Ensembl:ENSG00000180758 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,31158229,31158229 RNA-Seq:(High) rs1406371856 Functional Loss SNV dbSNP153 33..33 33 - - - 12576 RMVar_ID_12576 Human_SNP_ID_2516067 A-to-I Human chr1 - 9100942 9100942 9100942 CAGTCTGGAGTGCAGTGATGCAATCATGGCTCACTGCAGCCTCCACCTCCCAGGCTCAAGCGATC CAGTCTGGAGTGCAGTGATGCAATCATGGCTCCCTGCAGCCTCCACCTCCCAGGCTCAAGCGATC T G GPR157 Ensembl:ENSG00000180758 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1406889378 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26384202 12577 RMVar_ID_12577 Human_SNP_ID_2516070 A-to-I Human chr1 - 9100952 9100952 9100952 GCATCATACCCAGTCTGGAGTGCAGTGATGCAATCATGGCTCACTGCAGCCTCCACCTCCCAGGC GCATCATACCCAGTCTGGAGTGCAGTGATGCAGTCATGGCTCACTGCAGCCTCCACCTCCCAGGC T C GPR157 Ensembl:ENSG00000180758 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs558720474 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26384202 12578 RMVar_ID_12578 Human_SNP_ID_2516079 A-to-I Human chr1 - 9101015 9101015 9101015 AGGAGGGGCTGTTACTTCTTTTTAGTTTATTTATTTTTGTGAGGCAGGGTTTTGCTGTCTGGAGC AGGAGGGGCTGTTACTTCTTTTTAGTTTATTTTTTTTTGTGAGGCAGGGTTTTGCTGTCTGGAGC T A GPR157 Ensembl:ENSG00000180758 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1330855311 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5880923 12579 RMVar_ID_12579 Human_SNP_ID_2516093 A-to-I Human chr1 - 9101083 9101083 9101083 AGACTGCACCACTGCACTCCAGCCTGGGTGACAGAGCAAGACTCCATCTCAAAAAATAAAACAAG AGACTGCACCACTGCACTCCAGCCTGGGTGACGGAGCAAGACTCCATCTCAAAAAATAAAACAAG T C GPR157 Ensembl:ENSG00000180758 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1430200920 Functional Loss SNV dbSNP153 33..33 33 - - - 12580 RMVar_ID_12580 Human_SNP_ID_2516114 A-to-I Human chr1 - 9101172 9101172 9101172 GTGGTTTCGTGTGCCTGTAGTGCCAGCTACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAACCCA GTGGTTTCGTGTGCCTGTAGTGCCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCTTGAACCCA T C GPR157 Ensembl:ENSG00000180758 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs990477352 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17556934 12581 RMVar_ID_12581 Human_SNP_ID_2516123 A-to-I Human chr1 - 9101212 9101211 9101213 GTTTCTACTAAATATACAAAAAAAAAAAAAATAGTTGGATGTGGTTTCGTGTGCCTGTAGTGCCA GTTTCTACTAAATATACAAAAAAAAAAAAAA__GTTGGATGTGGTTTCGTGTGCCTGTAGTGCCA CTA C GPR157 Ensembl:ENSG00000180758 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs745605631 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_5880926 12582 RMVar_ID_12582 Human_SNP_ID_2516161 A-to-I Human chr1 - 9101307 9101307 9101307 TCACGCCTGTAATCCCAGCACTTTGGGAGACCAAGGTGGGCAGATCACCTGAGGTCAGGAGTTTG TCACGCCTGTAATCCCAGCACTTTGGGAGACCGAGGTGGGCAGATCACCTGAGGTCAGGAGTTTG T C GPR157 Ensembl:ENSG00000180758 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs374897685 Functional Loss SNV dbSNP153 33..33 33 - - - 12583 RMVar_ID_12583 Human_SNP_ID_2516387 A-to-I Human chr1 - 9102364 9102364 9102364 CTCTATTGCCCAGGCTGGAGTGCAGTGGTGCAATTTTGACTCACTGCAACCACCGCCTCCCAGGT CTCTATTGCCCAGGCTGGAGTGCAGTGGTGCAGTTTTGACTCACTGCAACCACCGCCTCCCAGGT T C GPR157 Ensembl:ENSG00000180758 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs974287729 Functional Loss SNV dbSNP153 33..33 33 - - - 12584 RMVar_ID_12584 Human_SNP_ID_2516394 A-to-I Human chr1 - 9102392 9102392 9102392 TTTTTTTTTTTTTTGAGATGGAGTCTCACTCTATTGCCCAGGCTGGAGTGCAGTGGTGCAATTTT TTTTTTTTTTTTTTGAGATGGAGTCTCACTCTGTTGCCCAGGCTGGAGTGCAGTGGTGCAATTTT T C GPR157 Ensembl:ENSG00000180758 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1316157060 Functional Loss SNV dbSNP153 33..33 33 - - - 12585 RMVar_ID_12585 Human_SNP_ID_2516569 A-to-I Human chr1 - 9103051 9103051 9103051 CGCCCGGAGCTGATGTGGTGGTGCGTGCCTGTAGTCCCTACTACTCAGGAGGCTGAGACGGGAGG CGCCCGGAGCTGATGTGGTGGTGCGTGCCTGTGGTCCCTACTACTCAGGAGGCTGAGACGGGAGG T C GPR157 Ensembl:ENSG00000180758 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1224778611 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11148506,Human_RBP_ID_17760645,Human_RBP_ID_26384210 Human_miRNA_ID_274425 12586 RMVar_ID_12586 Human_SNP_ID_2520689 A-to-I Human chr1 - 9116968 9116968 9116968 GAGAGGCCAGGGCGAGAAGATAACTTGAAGCCAGGAGTTCAAGACCAGCCTGGGCAATAAAGCAA GAGAGGCCAGGGCGAGAAGATAACTTGAAGCCTGGAGTTCAAGACCAGCCTGGGCAATAAAGCAA T A GPR157 Ensembl:ENSG00000180758 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs188495812 Functional Loss SNV dbSNP153 33..33 33 - - - 12587 RMVar_ID_12587 Human_SNP_ID_2521123 A-to-I Human chr1 - 9118854 9118854 9118854 ATTTATGTATTTTTTTGTAGAGACAGGGTCTCACTTTGTTGCCCAGGCTGGTCTCAAACTCTCCT ATTTATGTATTTTTTTGTAGAGACAGGGTCTCCCTTTGTTGCCCAGGCTGGTCTCAAACTCTCCT T G GPR157 Ensembl:ENSG00000180758 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1423550537 Functional Loss SNV dbSNP153 33..33 33 - - - 12588 RMVar_ID_12588 Human_SNP_ID_2529360 A-to-I Human chr1 - 9149398 9149398 9149398 AAAAAATACAAAAATTAGCCAGGCATAGTGGCAGGACTGTAGTCCCAGCTACTCAGGAGGCTGAG AAAAAATACAAAAATTAGCCAGGCATAGTGGCGGGACTGTAGTCCCAGCTACTCAGGAGGCTGAG T C MIR34AHG Ensembl:ENSG00000228526 lincRNA exon GSE123020:GSM3490829,GSM3490830,GSM3490831 esophageal squamous carcinoma cells,EC109 cell line - 32596459 RNA-Seq:(High) rs916722019 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5245760,Human_RBP_ID_11149851 12589 RMVar_ID_12589 Human_SNP_ID_2529365 A-to-I Human chr1 - 9149404 9149404 9149404 CTCTACAAAAAATACAAAAATTAGCCAGGCATAGTGGCAGGACTGTAGTCCCAGCTACTCAGGAG CTCTACAAAAAATACAAAAATTAGCCAGGCATCGTGGCAGGACTGTAGTCCCAGCTACTCAGGAG T G MIR34AHG Ensembl:ENSG00000228526 lincRNA exon GSE123020:GSM3490829,GSM3490830,GSM3490831 esophageal squamous carcinoma cells,EC109 cell line - 32596459 RNA-Seq:(High) rs1241021363 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5245760,Human_RBP_ID_11149851 12590 RMVar_ID_12590 Human_SNP_ID_2529384 A-to-I Human chr1 - 9149509 9149509 9149509 GTCTGGGTTGGGCACGGTGGCGCATGCCTGTAATCCCAGCACTTGGGGAGGCCCAGGTGGATGGA GTCTGGGTTGGGCACGGTGGCGCATGCCTGTACTCCCAGCACTTGGGGAGGCCCAGGTGGATGGA T G MIR34AHG Ensembl:ENSG00000228526 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1157965495 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5245760 12591 RMVar_ID_12591 Human_SNP_ID_2530634 A-to-I Human chr1 - 9154862 9154862 9154862 GAGCCACCATCCAATTTTTTATTTTTATTTTTAGAGACAGGGTCTTGCTCTGTCACCCAGGCTAG GAGCCACCATCCAATTTTTTATTTTTATTTTTGGAGACAGGGTCTTGCTCTGTCACCCAGGCTAG T C MIR34AHG Ensembl:ENSG00000228526 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs576422850 Functional Loss SNV dbSNP153 33..33 33 - - - 12592 RMVar_ID_12592 Human_SNP_ID_2531473 A-to-I Human chr1 - 9157999 9157999 9157999 CTCCTGCCTCACAGGCGTGCACCACCATGCCCAGCTCACTTTTTAATTTTTTGTAGAGATAGCAC CTCCTGCCTCACAGGCGTGCACCACCATGCCCCGCTCACTTTTTAATTTTTTGTAGAGATAGCAC T G MIR34AHG Ensembl:ENSG00000228526 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs942137840 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8241814 12593 RMVar_ID_12593 Human_SNP_ID_2531958 A-to-I Human chr1 - 9159973 9159973 9159973 TTTTTTTTTTTTAAGAAATTCTCACCAGGCACAGTGGCTCATGCCTGTAATCCCAGCACTTTGGG TTTTTTTTTTTTAAGAAATTCTCACCAGGCACCGTGGCTCATGCCTGTAATCCCAGCACTTTGGG T G MIR34AHG Ensembl:ENSG00000228526 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1267894993 Functional Loss SNV dbSNP153 33..33 33 - - - 12594 RMVar_ID_12594 Human_SNP_ID_2534783 A-to-I Human chr1 - 9170518 9170518 9170518 GTTTTTTTATAATTTTTTTGAGACAGAGTCTCACACTGTCACCTGGGCTGGAGTGCAATGGCATG GTTTTTTTATAATTTTTTTGAGACAGAGTCTCGCACTGTCACCTGGGCTGGAGTGCAATGGCATG T C MIR34AHG Ensembl:ENSG00000228526 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1409823578 Functional Loss SNV dbSNP153 33..33 33 - - - 12595 RMVar_ID_12595 Human_SNP_ID_2534873 A-to-I Human chr1 - 9170886 9170886 9170886 TTATGAATTAGGTGTACTTGGCCGGGCACGGTAGCTCACGCCTGTAATCTCAGCACTTTGGGAGG TTATGAATTAGGTGTACTTGGCCGGGCACGGTGGCTCACGCCTGTAATCTCAGCACTTTGGGAGG T C MIR34AHG Ensembl:ENSG00000228526 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1051144975 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11151156,Human_RBP_ID_22707929 12596 RMVar_ID_12596 Human_SNP_ID_2535218 A-to-I Human chr1 - 9172488 9172488 9172488 GGAAGGCTGGGGCAGAATTGCTTGAACCTGGGAGGCGGAGATTGCAGTGAGCCAAGATCATGCCA GGAAGGCTGGGGCAGAATTGCTTGAACCTGGGGGGCGGAGATTGCAGTGAGCCAAGATCATGCCA T C MIR34AHG Ensembl:ENSG00000228526 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1409155461 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8241894 12597 RMVar_ID_12597 Human_SNP_ID_2535256 A-to-I Human chr1 - 9172642 9172642 9172642 CTGTAATCCCAGCACTTTTGGGAGGCTGAGGCAGGTGGATCATCTGAGGTCACGAGTTCGAGACC CTGTAATCCCAGCACTTTTGGGAGGCTGAGGCGGGTGGATCATCTGAGGTCACGAGTTCGAGACC T C MIR34AHG Ensembl:ENSG00000228526 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1448703088 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11151439,Human_RBP_ID_24738623 12598 RMVar_ID_12598 Human_SNP_ID_2536106 A-to-I Human chr1 - 9176349 9176349 9176349 ACCACACCCAACTAATTTTTTAAATTTTTCGTAGGGGCAGTGTCTCATTATGTTGCCCAGGCTGG ACCACACCCAACTAATTTTTTAAATTTTTCGTTGGGGCAGTGTCTCATTATGTTGCCCAGGCTGG T A MIR34AHG Ensembl:ENSG00000228526 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs975402119 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11151625,Human_RBP_ID_17556943,Human_RBP_ID_24738652 12599 RMVar_ID_12599 Human_SNP_ID_2536110 A-to-I Human chr1 - 9176360 9176360 9176360 TTTACATGTGCACCACACCCAACTAATTTTTTAAATTTTTCGTAGGGGCAGTGTCTCATTATGTT TTTACATGTGCACCACACCCAACTAATTTTTTTAATTTTTCGTAGGGGCAGTGTCTCATTATGTT T A MIR34AHG Ensembl:ENSG00000228526 lincRNA intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs934261084 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11151625 12600 RMVar_ID_12600 Human_SNP_ID_2536394 A-to-I Human chr1 - 9177465 9177465 9177465 CCCCGTCTGTACTAAAAATGCAAAAATCAGCCAGGTGTGGTGGCAGGTGCCTGTAATCCCAGATA CCCCGTCTGTACTAAAAATGCAAAAATCAGCCGGGTGTGGTGGCAGGTGCCTGTAATCCCAGATA T C MIR34AHG Ensembl:ENSG00000228526 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs867873107 Functional Loss SNV dbSNP153 33..33 33 - - - 12601 RMVar_ID_12601 Human_SNP_ID_2540507 A-to-I Human chr1 + 9194019 9194019 9194019 CAGTGGCATGATCTCGGCTCTCTGCAACCTCCACCTCCCTGGCTCAAGCTAGCCTCCTACCTCAG CAGTGGCATGATCTCGGCTCTCTGCAACCTCCGCCTCCCTGGCTCAAGCTAGCCTCCTACCTCAG A G LNCTAM34A Ensembl:ENSG00000234546 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs542955083 Functional Loss SNV dbSNP153 33..33 33 - - - 12602 RMVar_ID_12602 Human_SNP_ID_2551766 A-to-I Human chr1 + 9236270 9236270 9236270 CCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAACCACCGCGCCCAGCTGGTTAGTTGGTTT CCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAACCACCGCGCCCAGCTGGTTAGTTGGTTT A G H6PD Ensembl:ENSG00000049239 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1057123973 Functional Loss SNV dbSNP153 33..33 33 - - - 12603 RMVar_ID_12603 Human_SNP_ID_2552073 A-to-I Human chr1 + 9237296 9237296 9237296 AGATGGAGTCTTGCTCTGTTGCCCAGGGGCGCAATCTCAGCTCACTGCAACGTTCGCCTCCTAGG AGATGGAGTCTTGCTCTGTTGCCCAGGGGCGCGATCTCAGCTCACTGCAACGTTCGCCTCCTAGG A G H6PD Ensembl:ENSG00000049239 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs906112016 Functional Loss SNV dbSNP153 33..33 33 - - - 12604 RMVar_ID_12604 Human_SNP_ID_2560699 A-to-I Human chr1 + 9266937 9266937 9266937 CCACCTCCCGGGTTCAGGCAATTCTCGTGCCTAAGCCTCCCGAGTAGCTGCGACTACAGGCGCCG CCACCTCCCGGGTTCAGGCAATTCTCGTGCCTGAGCCTCCCGAGTAGCTGCGACTACAGGCGCCG A G H6PD Ensembl:ENSG00000049239 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs149497526 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113746,RMVar_hsa_circ_94938,RMVar_hsa_circ_128797,RMVar_hsa_circ_128800,RMVar_hsa_circ_123281,RMVar_hsa_circ_128801 12605 RMVar_ID_12605 Human_SNP_ID_2560719 A-to-I Human chr1 + 9267003 9267003 9267003 CCAGCATGCCTGTCTAATTTTTGTATTTTAGTAGAGACAGGGTTTCACCATGTTGCCCAGGCTGG CCAGCATGCCTGTCTAATTTTTGTATTTTAGTGGAGACAGGGTTTCACCATGTTGCCCAGGCTGG A G H6PD Ensembl:ENSG00000049239 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1022695194 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113746,RMVar_hsa_circ_94938,RMVar_hsa_circ_128797,RMVar_hsa_circ_128800,RMVar_hsa_circ_123281,RMVar_hsa_circ_128801 12606 RMVar_ID_12606 Human_SNP_ID_2560737 A-to-I Human chr1 + 9267054 9267054 9267054 GTTGCCCAGGCTGGTCTCGAACTCCTGAGCTCAGGCAGTCTACCCACCTCAGCCTCCCAAAGTGC GTTGCCCAGGCTGGTCTCGAACTCCTGAGCTCGGGCAGTCTACCCACCTCAGCCTCCCAAAGTGC A G H6PD Ensembl:ENSG00000049239 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs990775617 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113746,RMVar_hsa_circ_94938,RMVar_hsa_circ_128797,RMVar_hsa_circ_128800,RMVar_hsa_circ_123281,RMVar_hsa_circ_128801 12607 RMVar_ID_12607 Human_SNP_ID_2561000 A-to-I Human chr1 + 9267987 9267987 9267987 ACTAAATTGGGCTAGGTGTGGCTCATGCCTGTAATCCCAGCACTATGGGAGGCTGAGGTGAGAGG ACTAAATTGGGCTAGGTGTGGCTCATGCCTGTGATCCCAGCACTATGGGAGGCTGAGGTGAGAGG A G H6PD Ensembl:ENSG00000049239 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,31158229,32596459 RNA-Seq:(High) rs887774006 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_14711 RMVar_hsa_circ_113746,RMVar_hsa_circ_94938,RMVar_hsa_circ_128797,RMVar_hsa_circ_128800,RMVar_hsa_circ_123281,RMVar_hsa_circ_128801 12608 RMVar_ID_12608 Human_SNP_ID_2561006 A-to-I Human chr1 + 9267999 9267999 9267999 TAGGTGTGGCTCATGCCTGTAATCCCAGCACTATGGGAGGCTGAGGTGAGAGGATCACTTGAGCC TAGGTGTGGCTCATGCCTGTAATCCCAGCACTGTGGGAGGCTGAGGTGAGAGGATCACTTGAGCC A G H6PD Ensembl:ENSG00000049239 Protein coding 3'UTR GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1002730146 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_14711 RMVar_hsa_circ_113746,RMVar_hsa_circ_94938,RMVar_hsa_circ_128797,RMVar_hsa_circ_128800,RMVar_hsa_circ_123281,RMVar_hsa_circ_128801 12609 RMVar_ID_12609 Human_SNP_ID_2561007 A-to-I Human chr1 + 9267999 9267999 9267999 TAGGTGTGGCTCATGCCTGTAATCCCAGCACTATGGGAGGCTGAGGTGAGAGGATCACTTGAGCC TAGGTGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGAGAGGATCACTTGAGCC A T H6PD Ensembl:ENSG00000049239 Protein coding 3'UTR GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1002730146 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_14711 RMVar_hsa_circ_113746,RMVar_hsa_circ_94938,RMVar_hsa_circ_128797,RMVar_hsa_circ_128800,RMVar_hsa_circ_123281,RMVar_hsa_circ_128801 12610 RMVar_ID_12610 Human_SNP_ID_2561016 A-to-I Human chr1 + 9268043 9268043 9268043 GGTGAGAGGATCACTTGAGCCCAGAAGGTTGAAACCAGCCTGGGCAACATAGTGAGACCCCATCT GGTGAGAGGATCACTTGAGCCCAGAAGGTTGAGACCAGCCTGGGCAACATAGTGAGACCCCATCT A G H6PD Ensembl:ENSG00000049239 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1142685 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113746,RMVar_hsa_circ_94938,RMVar_hsa_circ_128797,RMVar_hsa_circ_128800,RMVar_hsa_circ_123281,RMVar_hsa_circ_128801 12611 RMVar_ID_12611 Human_SNP_ID_2561021 A-to-I Human chr1 + 9268061 9268061 9268061 GCCCAGAAGGTTGAAACCAGCCTGGGCAACATAGTGAGACCCCATCTCTACAAAAAGTTTTAAAA GCCCAGAAGGTTGAAACCAGCCTGGGCAACATGGTGAGACCCCATCTCTACAAAAAGTTTTAAAA A G H6PD Ensembl:ENSG00000049239 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1142687 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113746,RMVar_hsa_circ_94938,RMVar_hsa_circ_128797,RMVar_hsa_circ_128800,RMVar_hsa_circ_123281,RMVar_hsa_circ_128801 12612 RMVar_ID_12612 Human_SNP_ID_2561044 A-to-I Human chr1 + 9268141 9268141 9268141 CCCTCCTGTGGTCCCAGCTACTCGGGAGTCTGAGGTGGGAGGATCACCTGAGCCCAGGAGACTGA CCCTCCTGTGGTCCCAGCTACTCGGGAGTCTGTGGTGGGAGGATCACCTGAGCCCAGGAGACTGA A T H6PD Ensembl:ENSG00000049239 Protein coding 3'UTR GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs924402500 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113746,RMVar_hsa_circ_94938,RMVar_hsa_circ_128797,RMVar_hsa_circ_128800,RMVar_hsa_circ_123281,RMVar_hsa_circ_128801 12613 RMVar_ID_12613 Human_SNP_ID_2561072 A-to-I Human chr1 + 9268234 9268234 9268234 GCTCTCTAGCCTGGAAAACAGAGTGAGACCCTATCTCAAAAAAAAAAAAAAAAAAAAAGGAAAGA GCTCTCTAGCCTGGAAAACAGAGTGAGACCCTGTCTCAAAAAAAAAAAAAAAAAAAAAGGAAAGA A G H6PD Ensembl:ENSG00000049239 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs147750192 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_95539 RMVar_hsa_circ_113746,RMVar_hsa_circ_94938,RMVar_hsa_circ_128797,RMVar_hsa_circ_128800,RMVar_hsa_circ_123281,RMVar_hsa_circ_128801 12614 RMVar_ID_12614 Human_SNP_ID_2572125 A-to-I Human chr1 + 9309722 9309718 9309723 AAAATTAGTCGGGGATGGTGGTGCATGCCCATAATCCCACTACTTGGGAGGCTGAGGCAGGAGAA AAAATTAGTCGGGGATGGTGGTGCATGCC_____TCCCACTACTTGGGAGGCTGAGGCAGGAGAA CCATAA C SPSB1 Ensembl:ENSG00000171621 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1414742899 Functional Loss DEL dbSNP153 30..34 33 - - - RMVar_hsa_circ_128803,RMVar_hsa_circ_116564 12615 RMVar_ID_12615 Human_SNP_ID_2638440 A-to-I Human chr1 + 9557540 9557540 9557540 GGGCAATGTGGCGAAATCCCATCTCTACAAAAAATACAAAAAATTAGCCGGGCATGTTGGCGTGC GGGCAATGTGGCGAAATCCCATCTCTACAAAAGATACAAAAAATTAGCCGGGCATGTTGGCGTGC A G SLC25A33 Ensembl:ENSG00000171612 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs767173581 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108002,RMVar_hsa_circ_307915,RMVar_hsa_circ_312840,RMVar_hsa_circ_272681,RMVar_hsa_circ_128806 12616 RMVar_ID_12616 Human_SNP_ID_2638441 A-to-I Human chr1 + 9557540 9557540 9557540 GGGCAATGTGGCGAAATCCCATCTCTACAAAAAATACAAAAAATTAGCCGGGCATGTTGGCGTGC GGGCAATGTGGCGAAATCCCATCTCTACAAAATATACAAAAAATTAGCCGGGCATGTTGGCGTGC A T SLC25A33 Ensembl:ENSG00000171612 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs767173581 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108002,RMVar_hsa_circ_307915,RMVar_hsa_circ_312840,RMVar_hsa_circ_272681,RMVar_hsa_circ_128806 12617 RMVar_ID_12617 Human_SNP_ID_2640737 A-to-I Human chr1 + 9565757 9565757 9565757 AAAATTAGCCGGGCGTGGTGGCGGGTGCCTGTAGTCCCAGCTGCTCGGGGGGCTGAGGCAGGAGA AAAATTAGCCGGGCGTGGTGGCGGGTGCCTGTTGTCCCAGCTGCTCGGGGGGCTGAGGCAGGAGA A T SLC25A33 Ensembl:ENSG00000171612 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1329421879 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108002,RMVar_hsa_circ_307915,RMVar_hsa_circ_312840,RMVar_hsa_circ_272681,RMVar_hsa_circ_128806 12618 RMVar_ID_12618 Human_SNP_ID_2642791 A-to-I Human chr1 + 9573665 9573665 9573665 ATCTCTGGTTGTGTCCCCTGATCCGCAGTCCCACCTGTTGTCTCAGAGAGTCAGTGACTGTCTCT ATCTCTGGTTGTGTCCCCTGATCCGCAGTCCCGCCTGTTGTCTCAGAGAGTCAGTGACTGTCTCT A G SLC25A33 Ensembl:ENSG00000171612 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6540953 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_999 RMVar_hsa_circ_88462,RMVar_hsa_circ_108002,RMVar_hsa_circ_272681,RMVar_hsa_circ_128806,RMVar_hsa_circ_350307,RMVar_hsa_circ_376056,RMVar_hsa_circ_128807,RMVar_hsa_circ_128808,RMVar_hsa_circ_352133 12619 RMVar_ID_12619 Human_SNP_ID_2642792 A-to-I Human chr1 + 9573665 9573665 9573665 ATCTCTGGTTGTGTCCCCTGATCCGCAGTCCCACCTGTTGTCTCAGAGAGTCAGTGACTGTCTCT ATCTCTGGTTGTGTCCCCTGATCCGCAGTCCCTCCTGTTGTCTCAGAGAGTCAGTGACTGTCTCT A T SLC25A33 Ensembl:ENSG00000171612 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6540953 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_999 RMVar_hsa_circ_88462,RMVar_hsa_circ_108002,RMVar_hsa_circ_272681,RMVar_hsa_circ_128806,RMVar_hsa_circ_350307,RMVar_hsa_circ_376056,RMVar_hsa_circ_128807,RMVar_hsa_circ_128808,RMVar_hsa_circ_352133 12620 RMVar_ID_12620 Human_SNP_ID_2642867 A-to-I Human chr1 + 9574023 9574019 9574023 TGTTTTGTTTTTTTGTTTTGAGATAGGGTCTTACTTGTTGCCGAAGCTGAAGTGCAGTGGTCCAA TGTTTTGTTTTTTTGTTTTGAGATAGGGT____CTTGTTGCCGAAGCTGAAGTGCAGTGGTCCAA TCTTA T SLC25A33 Ensembl:ENSG00000171612 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs984558330 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_88462,RMVar_hsa_circ_108002,RMVar_hsa_circ_272681,RMVar_hsa_circ_128806,RMVar_hsa_circ_350307,RMVar_hsa_circ_376056,RMVar_hsa_circ_128807,RMVar_hsa_circ_128808,RMVar_hsa_circ_352133 12621 RMVar_ID_12621 Human_SNP_ID_2642869 A-to-I Human chr1 + 9574023 9574023 9574023 TGTTTTGTTTTTTTGTTTTGAGATAGGGTCTTACTTGTTGCCGAAGCTGAAGTGCAGTGGTCCAA TGTTTTGTTTTTTTGTTTTGAGATAGGGTCTTTCTTGTTGCCGAAGCTGAAGTGCAGTGGTCCAA A T SLC25A33 Ensembl:ENSG00000171612 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1373351707 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88462,RMVar_hsa_circ_108002,RMVar_hsa_circ_272681,RMVar_hsa_circ_128806,RMVar_hsa_circ_350307,RMVar_hsa_circ_376056,RMVar_hsa_circ_128807,RMVar_hsa_circ_128808,RMVar_hsa_circ_352133 12622 RMVar_ID_12622 Human_SNP_ID_2642937 A-to-I Human chr1 + 9574233 9574233 9574233 CCTCAGCCTCACCTCCTCAGTAGTTTGAGACCACAGGTGCATGCCACCACACCCAGCTAATTTTG CCTCAGCCTCACCTCCTCAGTAGTTTGAGACCGCAGGTGCATGCCACCACACCCAGCTAATTTTG A G SLC25A33 Ensembl:ENSG00000171612 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs147457612 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88462,RMVar_hsa_circ_108002,RMVar_hsa_circ_272681,RMVar_hsa_circ_128806,RMVar_hsa_circ_350307,RMVar_hsa_circ_376056,RMVar_hsa_circ_128807,RMVar_hsa_circ_128808,RMVar_hsa_circ_352133 12623 RMVar_ID_12623 Human_SNP_ID_2644892 A-to-I Human chr1 + 9581923 9581923 9581923 AGACACAGTTGTAACCTTGACAATTTTATTTTATTTATTTATTTTTTGAGACAGAGTCTTGCTTG AGACACAGTTGTAACCTTGACAATTTTATTTTGTTTATTTATTTTTTGAGACAGAGTCTTGCTTG A G SLC25A33 Ensembl:ENSG00000171612 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs887382714 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5887557 RMVar_hsa_circ_88462,RMVar_hsa_circ_108002,RMVar_hsa_circ_128806,RMVar_hsa_circ_128807 12624 RMVar_ID_12624 Human_SNP_ID_2645192 A-to-I Human chr1 + 9583063 9583063 9583063 CCTGGCCAACATGGCGAAACCCTGTCTCTACTAAAAATACAAAAATTAGCCGGACGTGTGCCTGT CCTGGCCAACATGGCGAAACCCTGTCTCTACTGAAAATACAAAAATTAGCCGGACGTGTGCCTGT A G SLC25A33 Ensembl:ENSG00000171612 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs552968460 Functional Loss SNV dbSNP153 33..33 33 - - - 12625 RMVar_ID_12625 Human_SNP_ID_2675729 A-to-I Human chr1 + 9697829 9697829 9697829 GAGGCGGGTGGAGCACTTGAAGTCAGGAGTTCAAGATCAGCCTGAGCAACATGGCAAAACTCTGT GAGGCGGGTGGAGCACTTGAAGTCAGGAGTTCGAGATCAGCCTGAGCAACATGGCAAAACTCTGT A G PIK3CD Ensembl:ENSG00000171608 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1456927110 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27102 12626 RMVar_ID_12626 Human_SNP_ID_2677245 A-to-I Human chr1 + 9704549 9704549 9704549 TTTGTTTTGTTTTTGAGACAGGGTCTCACTCTATTGCCCAGGCTGGAGTGCAGTGGCACAATCTC TTTGTTTTGTTTTTGAGACAGGGTCTCACTCTGTTGCCCAGGCTGGAGTGCAGTGGCACAATCTC A G PIK3CD Ensembl:ENSG00000171608 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs568009616 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27102 12627 RMVar_ID_12627 Human_SNP_ID_2677453 A-to-I Human chr1 + 9705413 9705413 9705413 CAGCTACCTGGGAGCCTGAGGTTGGGAGGATCACCTGAGCCTGGGAGGTTGAGGCTGCAGTGAGC CAGCTACCTGGGAGCCTGAGGTTGGGAGGATCGCCTGAGCCTGGGAGGTTGAGGCTGCAGTGAGC A G PIK3CD Ensembl:ENSG00000171608 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs148864408 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27102 12628 RMVar_ID_12628 Human_SNP_ID_2677696 A-to-I Human chr1 + 9706386 9706386 9706386 ATGGTGGCACAAGCCTGTAGTCTCAGCCACTCAGGAGGCTGAGGCTGGAGGATCGCTTGAGCCCA ATGGTGGCACAAGCCTGTAGTCTCAGCCACTCGGGAGGCTGAGGCTGGAGGATCGCTTGAGCCCA A G PIK3CD Ensembl:ENSG00000171608 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs773116906 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_102585 RMVar_hsa_circ_27102 12629 RMVar_ID_12629 Human_SNP_ID_2678174 A-to-I Human chr1 + 9708215 9708211 9708215 TGTTTGTTTGTTTGTTTGTTTGAGACAGTCTCACTCTGTCATCCAGGCTGGAGTGCAGTGGCGCA TGTTTGTTTGTTTGTTTGTTTGAGACAGT____CTCTGTCATCCAGGCTGGAGTGCAGTGGCGCA TCTCA T PIK3CD Ensembl:ENSG00000171608 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1458362275 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_27102 12630 RMVar_ID_12630 Human_SNP_ID_2678485 A-to-I Human chr1 + 9709643 9709643 9709643 GGGAACATCGCTTGAACCTAGGAATTTGTGTTACAGTGAGCTATGATGGCACCACTGTACTCCAG GGGAACATCGCTTGAACCTAGGAATTTGTGTTTCAGTGAGCTATGATGGCACCACTGTACTCCAG A T PIK3CD Ensembl:ENSG00000171608 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs979367496 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27102 12631 RMVar_ID_12631 Human_SNP_ID_2679273 A-to-I Human chr1 + 9712778 9712778 9712778 TAGGAAAAGGCCTGGCATGGTGGCTCATGCCTATAATCCCAGAACTTTGGGAGGCTGAGGCAGGA TAGGAAAAGGCCTGGCATGGTGGCTCATGCCTGTAATCCCAGAACTTTGGGAGGCTGAGGCAGGA A G PIK3CD Ensembl:ENSG00000171608 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1473202499 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79751,RMVar_hsa_circ_128814,RMVar_hsa_circ_266583 12632 RMVar_ID_12632 Human_SNP_ID_2679327 A-to-I Human chr1 + 9713062 9713062 9713062 AAAATTAGCCAGGTGTGGTGGTAGATGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCCGAAGA AAAATTAGCCAGGTGTGGTGGTAGATGCCTGTGATCCCAGCTACTCGGGAGGCTGAGGCCGAAGA A G PIK3CD Ensembl:ENSG00000171608 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1478155460 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79751,RMVar_hsa_circ_128814,RMVar_hsa_circ_266583 12633 RMVar_ID_12633 Human_SNP_ID_2679366 A-to-I Human chr1 + 9713257 9713257 9713257 CTAGCTACTCAGGAAGCTGAGGCAGGAGGATCACTTGAGCCTGGGAGTTTGAGGCTGCAGTGAGC CTAGCTACTCAGGAAGCTGAGGCAGGAGGATCGCTTGAGCCTGGGAGTTTGAGGCTGCAGTGAGC A G PIK3CD Ensembl:ENSG00000171608 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs896005003 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79751,RMVar_hsa_circ_128814,RMVar_hsa_circ_266583 12634 RMVar_ID_12634 Human_SNP_ID_2679561 A-to-I Human chr1 + 9714086 9714086 9714086 GTTGCCCAGGCTGGCCGTGAACTCCTGTGCTCAAGTGATCCTCCCACCTCAGCCTCCCAAAGTAT GTTGCCCAGGCTGGCCGTGAACTCCTGTGCTCGAGTGATCCTCCCACCTCAGCCTCCCAAAGTAT A G PIK3CD Ensembl:ENSG00000171608 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1331876972 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79751,RMVar_hsa_circ_128814,RMVar_hsa_circ_266583 12635 RMVar_ID_12635 Human_SNP_ID_2679565 A-to-I Human chr1 + 9714104 9714104 9714104 GAACTCCTGTGCTCAAGTGATCCTCCCACCTCAGCCTCCCAAAGTATTGGGATTACAGGAGTAAG GAACTCCTGTGCTCAAGTGATCCTCCCACCTCTGCCTCCCAAAGTATTGGGATTACAGGAGTAAG A T PIK3CD Ensembl:ENSG00000171608 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1209676838 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79751,RMVar_hsa_circ_128814,RMVar_hsa_circ_266583 12636 RMVar_ID_12636 Human_SNP_ID_2684656 A-to-I Human chr1 - 9730512 9730512 9730512 GCAGCTGGAGTGGGATGACTCCACCCTCAGCTACTGACCCGTGCCCCCGGCCACCTCGGTTTCTG GCAGCTGGAGTGGGATGACTCCACCCTCAGCTGCTGACCCGTGCCCCCGGCCACCTCGGTTTCTG T C CLSTN1 Ensembl:ENSG00000171603 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs753256517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_366718,Human_RBP_ID_4071896 RMVar_hsa_circ_85258,RMVar_hsa_circ_121065,RMVar_hsa_circ_107315,RMVar_hsa_circ_128820,RMVar_hsa_circ_128821,RMVar_hsa_circ_128822 12637 RMVar_ID_12637 Human_SNP_ID_2709336 A-to-I Human chr1 - 9817198 9817198 9817198 CATGAATCATTATCTTAAAAAGAATTAATAGAAGTGGCGTCTCACTGTGTTGCTCAGGCTGGTCT CATGAATCATTATCTTAAAAAGAATTAATAGACGTGGCGTCTCACTGTGTTGCTCAGGCTGGTCT T G CLSTN1 Ensembl:ENSG00000171603 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1484714323 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107315,RMVar_hsa_circ_128820,RMVar_hsa_circ_77987,RMVar_hsa_circ_128832 12638 RMVar_ID_12638 Human_SNP_ID_2710160 A-to-I Human chr1 - 9820263 9820263 9820263 CGCCTGCCTCTGCCTCCCACAGTGCTGAGATTACAGGTGTGAGCCACTGCACCCGGCCCAAACTT CGCCTGCCTCTGCCTCCCACAGTGCTGAGATTGCAGGTGTGAGCCACTGCACCCGGCCCAAACTT T C CLSTN1 Ensembl:ENSG00000171603 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs908707588 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107315,RMVar_hsa_circ_128820,RMVar_hsa_circ_77987,RMVar_hsa_circ_128832 12639 RMVar_ID_12639 Human_SNP_ID_2719682 A-to-I Human chr1 - 9857638 9857638 9857638 CACCACCACATCTGGCTAATGTTTGTATTTTTAGTAGATACGGGGTTTCACCACGTTGGATAGGC CACCACCACATCTGGCTAATGTTTGTATTTTTGGTAGATACGGGGTTTCACCACGTTGGATAGGC T C CTNNBIP1 Ensembl:ENSG00000178585 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs549597386 Functional Loss SNV dbSNP153 33..33 33 - - - 12640 RMVar_ID_12640 Human_SNP_ID_2737142 A-to-I Human chr1 - 9927713 9927713 9927713 CGCCACTGCACTCCAGCCTGGGCGACAGACTGAGACACGGTCTCAAAAAAAAAAAAAAAAAAAAA CGCCACTGCACTCCAGCCTGGGCGACAGACTGGGACACGGTCTCAAAAAAAAAAAAAAAAAAAAA T C LZIC Ensembl:ENSG00000162441 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1357419595 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26384954 RMVar_hsa_circ_128844 12641 RMVar_ID_12641 Human_SNP_ID_2737173 A-to-I Human chr1 - 9927874 9927874 9927874 GATCAGGAGCTCAAGACCAGCCTGGCCAACACAGTGAAACTCCATCTCTACAAAAATTAGCCAGG GATCAGGAGCTCAAGACCAGCCTGGCCAACACGGTGAAACTCCATCTCTACAAAAATTAGCCAGG T C LZIC Ensembl:ENSG00000162441 Protein coding intron GSE38233;GSE100210;GSE99789;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,29796672,32596459 RNA-Seq:(High) rs1386362540 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128844 12642 RMVar_ID_12642 Human_SNP_ID_2737189 A-to-I Human chr1 - 9927937 9927929 9927938 CGGGCACAGTGGCTCACACCTGTAATCCCAGCACTTCAGGAGGCCAAGGCGGGCGGATCACAAGA CGGGCACAGTGGCTCACACCTGTAATCCCAG_________AGGCCAAGGCGGGCGGATCACAAGA TCCTGAAGTG T LZIC Ensembl:ENSG00000162441 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1217171993 Functional Loss DEL dbSNP153 32..40 33 - - - Human_RBP_ID_26384955 RMVar_hsa_circ_128844 12643 RMVar_ID_12643 Human_SNP_ID_2737191 A-to-I Human chr1 - 9927937 9927937 9927937 CGGGCACAGTGGCTCACACCTGTAATCCCAGCACTTCAGGAGGCCAAGGCGGGCGGATCACAAGA CGGGCACAGTGGCTCACACCTGTAATCCCAGCCCTTCAGGAGGCCAAGGCGGGCGGATCACAAGA T G LZIC Ensembl:ENSG00000162441 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1289804460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26384955 RMVar_hsa_circ_128844 12644 RMVar_ID_12644 Human_SNP_ID_2737193 A-to-I Human chr1 - 9927952 9927952 9927952 ATTCTTCCCACCAGTCGGGCACAGTGGCTCACACCTGTAATCCCAGCACTTCAGGAGGCCAAGGC ATTCTTCCCACCAGTCGGGCACAGTGGCTCACGCCTGTAATCCCAGCACTTCAGGAGGCCAAGGC T C LZIC Ensembl:ENSG00000162441 Protein coding intron GSE100210;GSE99789;GSE123020:GSM3490829,GSM3490830,GSM3490831 HepG2 cell line;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109 cell line - 29129909,29796672,32596459 RNA-Seq:(High) rs566708484 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26385166 RMVar_hsa_circ_128844 12645 RMVar_ID_12645 Human_SNP_ID_2737196 A-to-I Human chr1 - 9927962 9927962 9927962 GCCATAGAAGATTCTTCCCACCAGTCGGGCACAGTGGCTCACACCTGTAATCCCAGCACTTCAGG GCCATAGAAGATTCTTCCCACCAGTCGGGCACGGTGGCTCACACCTGTAATCCCAGCACTTCAGG T C LZIC Ensembl:ENSG00000162441 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs912791054 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23150992,Human_RBP_ID_26385166 RMVar_hsa_circ_128844 12646 RMVar_ID_12646 Human_SNP_ID_2737197 A-to-I Human chr1 - 9927962 9927962 9927962 GCCATAGAAGATTCTTCCCACCAGTCGGGCACAGTGGCTCACACCTGTAATCCCAGCACTTCAGG GCCATAGAAGATTCTTCCCACCAGTCGGGCACCGTGGCTCACACCTGTAATCCCAGCACTTCAGG T G LZIC Ensembl:ENSG00000162441 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs912791054 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23150992,Human_RBP_ID_26385166 RMVar_hsa_circ_128844 12647 RMVar_ID_12647 Human_SNP_ID_2737211 A-to-I Human chr1 - 9928037 9928019 9928038 GTGCTGGGATGATTACAGGCATGAGCCACCATACCCGGCCTGAGCCACCACACCCAGCCTACGTT GTGCTGGGATGATTACAGGCATGAGCCACCA___________________CACCCAGCCTACGTT GTGGTGGCTCAGGCCGGGTA G LZIC Ensembl:ENSG00000162441 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348837363 Functional Loss DEL dbSNP153 32..50 33 - - - Human_RBP_ID_23150993,Human_RBP_ID_26385167 RMVar_hsa_circ_128844 12648 RMVar_ID_12648 Human_SNP_ID_2737220 A-to-I Human chr1 - 9928049 9928049 9928049 CAACCTCCCAGAGTGCTGGGATGATTACAGGCATGAGCCACCATACCCGGCCTGAGCCACCACAC CAACCTCCCAGAGTGCTGGGATGATTACAGGCGTGAGCCACCATACCCGGCCTGAGCCACCACAC T C LZIC Ensembl:ENSG00000162441 Protein coding intron GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831 HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line - 29129909,32596459 RNA-Seq:(High) rs1459728065 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23150993,Human_RBP_ID_26384959 RMVar_hsa_circ_128844 12649 RMVar_ID_12649 Human_SNP_ID_2737228 A-to-I Human chr1 - 9928089 9928089 9928089 GCTGGTCTCGAACTCCTGACCTTAGGTGATCCACCCGCCTCAACCTCCCAGAGTGCTGGGATGAT GCTGGTCTCGAACTCCTGACCTTAGGTGATCCCCCCGCCTCAACCTCCCAGAGTGCTGGGATGAT T G LZIC Ensembl:ENSG00000162441 Protein coding intron GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831 HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line - 29129909,29796672,31158229,32596459 RNA-Seq:(High) rs971389832 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128844 12650 RMVar_ID_12650 Human_SNP_ID_2737277 A-to-I Human chr1 - 9928274 9928274 9928274 GAGTTTCACTCTGTTGCCCAGGCTGGAGTGCAATGGCGTGATCTCGGCTCACCACAACTTCTGCC GAGTTTCACTCTGTTGCCCAGGCTGGAGTGCAGTGGCGTGATCTCGGCTCACCACAACTTCTGCC T C LZIC Ensembl:ENSG00000162441 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs889161073 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128844 12651 RMVar_ID_12651 Human_SNP_ID_2737280 A-to-I Human chr1 - 9928287 9928287 9928287 GTTTTTTGAGATGGAGTTTCACTCTGTTGCCCAGGCTGGAGTGCAATGGCGTGATCTCGGCTCAC GTTTTTTGAGATGGAGTTTCACTCTGTTGCCCCGGCTGGAGTGCAATGGCGTGATCTCGGCTCAC T G LZIC Ensembl:ENSG00000162441 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs770147928 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128844 12652 RMVar_ID_12652 Human_SNP_ID_2737399 A-to-I Human chr1 - 9928791 9928791 9928791 CGCAATCTCAACCTCCGCCTCCCAGGTTCAAGAGATTCTCCTGCCTCAGCTTCCCAAGTAGCTGG CGCAATCTCAACCTCCGCCTCCCAGGTTCAAGTGATTCTCCTGCCTCAGCTTCCCAAGTAGCTGG T A LZIC Ensembl:ENSG00000162441 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs988759446 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17762249 RMVar_hsa_circ_128844 12653 RMVar_ID_12653 Human_SNP_ID_2737407 A-to-I Human chr1 - 9928827 9928827 9928827 AGTTTTACTCTTATTGCCCAGGCTGGAGTGCAATGGCGCAATCTCAACCTCCGCCTCCCAGGTTC AGTTTTACTCTTATTGCCCAGGCTGGAGTGCAGTGGCGCAATCTCAACCTCCGCCTCCCAGGTTC T C LZIC Ensembl:ENSG00000162441 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs911222371 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_366849,Human_RBP_ID_8167605,Human_RBP_ID_26385172 RMVar_hsa_circ_128844 12654 RMVar_ID_12654 Human_SNP_ID_2741683 A-to-I Human chr1 + 9944615 9944615 9944615 ATAGCTCACTGCAGCCTTGAACTCCTGGGCTCAAGCGATCCTCTGGCCTTGGCCCCTCAAAGTGT ATAGCTCACTGCAGCCTTGAACTCCTGGGCTCCAGCGATCCTCTGGCCTTGGCCCCTCAAAGTGT A C AL357140.2,NMNAT1 Ensembl:ENSG00000228150,Ensembl:ENSG00000173614 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1182863794 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8243190,Human_RBP_ID_17556951 12655 RMVar_ID_12655 Human_SNP_ID_2741921 A-to-I Human chr1 + 9945579 9945579 9945579 AAAATTAGCTGTGCATGGTGGCGTATGCCTGTAGTTCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTAGCTGTGCATGGTGGCGTATGCCTGTGGTTCCAGCTACTCGGGAGGCTGAGGCAGGAGA A G AL357140.2,NMNAT1 Ensembl:ENSG00000228150,Ensembl:ENSG00000173614 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1328802610 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8243666 12656 RMVar_ID_12656 Human_SNP_ID_2742026 A-to-I Human chr1 + 9946014 9946014 9946014 GGGCTCAAGTAATCCTCCCACCTTGGCCCCGCAAAGTGCCGGAATTACAGGCATGAGCCACCCCA GGGCTCAAGTAATCCTCCCACCTTGGCCCCGCCAAGTGCCGGAATTACAGGCATGAGCCACCCCA A C AL357140.2,NMNAT1 Ensembl:ENSG00000228150,Ensembl:ENSG00000173614 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1045119663 Functional Loss SNV dbSNP153 33..33 33 - - - 12657 RMVar_ID_12657 Human_SNP_ID_2742027 A-to-I Human chr1 + 9946014 9946014 9946014 GGGCTCAAGTAATCCTCCCACCTTGGCCCCGCAAAGTGCCGGAATTACAGGCATGAGCCACCCCA GGGCTCAAGTAATCCTCCCACCTTGGCCCCGCTAAGTGCCGGAATTACAGGCATGAGCCACCCCA A T AL357140.2,NMNAT1 Ensembl:ENSG00000228150,Ensembl:ENSG00000173614 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1045119663 Functional Loss SNV dbSNP153 33..33 33 - - - 12658 RMVar_ID_12658 Human_SNP_ID_2742593 A-to-I Human chr1 + 9948786 9948786 9948786 ATTCTCCTGCCTCAGCCTCCTAAGTAGCTGGTACAGGCACCCGCCACCATGCCTGGCTAATTTTT ATTCTCCTGCCTCAGCCTCCTAAGTAGCTGGTGCAGGCACCCGCCACCATGCCTGGCTAATTTTT A G AL357140.2,NMNAT1 Ensembl:ENSG00000228150,Ensembl:ENSG00000173614 lincRNA,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1217996885 Functional Loss SNV dbSNP153 33..33 33 - - - 12659 RMVar_ID_12659 Human_SNP_ID_2743082 A-to-I Human chr1 + 9950952 9950952 9950952 CTCTACTAAAAATACCAAAATTATCCAGGCATAGTGGCACACACCTTTAATTCCAGCTACTGGGG CTCTACTAAAAATACCAAAATTATCCAGGCATGGTGGCACACACCTTTAATTCCAGCTACTGGGG A G NMNAT1 Ensembl:ENSG00000173614 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1157432368 Functional Loss SNV dbSNP153 33..33 33 - - - 12660 RMVar_ID_12660 Human_SNP_ID_2743086 A-to-I Human chr1 + 9950968 9950968 9950968 AAAATTATCCAGGCATAGTGGCACACACCTTTAATTCCAGCTACTGGGGAGGCTGAGGCAGAAGA AAAATTATCCAGGCATAGTGGCACACACCTTTGATTCCAGCTACTGGGGAGGCTGAGGCAGAAGA A G NMNAT1 Ensembl:ENSG00000173614 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1307454698 Functional Loss SNV dbSNP153 33..33 33 - - - 12661 RMVar_ID_12661 Human_SNP_ID_2746402 A-to-I Human chr1 + 9963549 9963549 9963549 ATCCTGCCTCAGCCTCCCGAGTACCTGGGATTACAGGCGCACACCACCACGCCCAGCGAATTTTT ATCCTGCCTCAGCCTCCCGAGTACCTGGGATTTCAGGCGCACACCACCACGCCCAGCGAATTTTT A T NMNAT1 Ensembl:ENSG00000173614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1378315024 Functional Loss SNV dbSNP153 33..33 33 - - - 12662 RMVar_ID_12662 Human_SNP_ID_2746535 A-to-I Human chr1 + 9964139 9964139 9964139 GTCTCAAACTCCTGGCCTCAAGTGACCCACCTACCTCGGCCTCCCAAAGTGCAGGGATTACAGGT GTCTCAAACTCCTGGCCTCAAGTGACCCACCTCCCTCGGCCTCCCAAAGTGCAGGGATTACAGGT A C NMNAT1 Ensembl:ENSG00000173614 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1351900436 Functional Loss SNV dbSNP153 33..33 33 - - - 12663 RMVar_ID_12663 Human_SNP_ID_2749341 A-to-I Human chr1 + 9975380 9975380 9975380 AAAAATTAACCAGCATGGTGGCATGCGCCCGTAATCCCAGCTACTCAGGAGTCTGACTCAGGAGA AAAAATTAACCAGCATGGTGGCATGCGCCCGTCATCCCAGCTACTCAGGAGTCTGACTCAGGAGA A C NMNAT1 Ensembl:ENSG00000173614 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs534698874 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128854,RMVar_hsa_circ_272816,RMVar_hsa_circ_322750,RMVar_hsa_circ_126635,RMVar_hsa_circ_128853 12664 RMVar_ID_12664 Human_SNP_ID_2751230 A-to-I Human chr1 + 9982834 9982797 9982835 AAGCTTAAAAGTTTAGTAAAAATCGTCTGGGCACAGTGGCTCACGCCTGTAATCCCAGCACTTTG __________________________________AGTGGCTCACGCCTGTAATCCCAGCACTTTG AACTAAAGCTTAAAAGTTTAGTAAAAATCGTCTGGGCAC A NMNAT1 Ensembl:ENSG00000173614 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1262808974 Functional Loss DEL dbSNP153 1..34 33 - - - RMVar_hsa_circ_128854,RMVar_hsa_circ_126635,RMVar_hsa_circ_113775,RMVar_hsa_circ_128856 12665 RMVar_ID_12665 Human_SNP_ID_2751257 A-to-I Human chr1 + 9982896 9982895 9982897 TTGGGAGGCTGAGGCAGGTGGATCACGGGGTCAAGAGATCGAGACCATCCTGGCCAATATGGTGA TTGGGAGGCTGAGGCAGGTGGATCACGGGGTC__GAGATCGAGACCATCCTGGCCAATATGGTGA CAA C NMNAT1 Ensembl:ENSG00000173614 Protein coding intron GSE38233;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29796672,31158229,31158229 RNA-Seq:(High) rs1264924871 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_128854,RMVar_hsa_circ_126635,RMVar_hsa_circ_113775,RMVar_hsa_circ_128856 12666 RMVar_ID_12666 Human_SNP_ID_2751427 A-to-I Human chr1 + 9983445 9983445 9983445 GGGAGGCCTAAGTGGGTGGATCACGTGAGGTCAAGAGTTCAAGACCAGCCTGGCCAATATGGTGA GGGAGGCCTAAGTGGGTGGATCACGTGAGGTCCAGAGTTCAAGACCAGCCTGGCCAATATGGTGA A C AL603962.1,NMNAT1 Ensembl:ENSG00000241326,Ensembl:ENSG00000173614 lincRNA,Protein coding intron,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1186928703 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128854,RMVar_hsa_circ_126635,RMVar_hsa_circ_113775,RMVar_hsa_circ_128856 12667 RMVar_ID_12667 Human_SNP_ID_2751606 A-to-I Human chr1 + 9984221 9984221 9984221 AGGCACCCACTACCATGTCCGGCTAATTTTGTATTTTTAGTAGAGATGGGGTTTCGCCATGTTAG AGGCACCCACTACCATGTCCGGCTAATTTTGTGTTTTTAGTAGAGATGGGGTTTCGCCATGTTAG A G AL603962.1,NMNAT1 Ensembl:ENSG00000241326,Ensembl:ENSG00000173614 lincRNA,Protein coding intron,3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs544820855 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_95294 RMVar_hsa_circ_128854,RMVar_hsa_circ_126635,RMVar_hsa_circ_113775,RMVar_hsa_circ_128856 12668 RMVar_ID_12668 Human_SNP_ID_2771207 A-to-I Human chr1 + 10061332 10061332 10061332 CTGGAGTGCAAGTGGCATGATTTTGGCCCACTACAACCTCCGTTTCCTGGGTTTAAGCAATTCTC CTGGAGTGCAAGTGGCATGATTTTGGCCCACTGCAACCTCCGTTTCCTGGGTTTAAGCAATTCTC A G UBE4B Ensembl:ENSG00000130939 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs751983330 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90073,RMVar_hsa_circ_128859 12669 RMVar_ID_12669 Human_SNP_ID_2774306 A-to-I Human chr1 + 10074016 10074016 10074016 GTGGCTGTTCATAGGCGTGATCCTAGTGCACTACAGCTTAAAACTCCCAGGCTCAGATGATCCGT GTGGCTGTTCATAGGCGTGATCCTAGTGCACTGCAGCTTAAAACTCCCAGGCTCAGATGATCCGT A G UBE4B Ensembl:ENSG00000130939 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1395626911 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90073,RMVar_hsa_circ_128859,RMVar_hsa_circ_319612,RMVar_hsa_circ_353688,RMVar_hsa_circ_12294,RMVar_hsa_circ_128860 12670 RMVar_ID_12670 Human_SNP_ID_2775820 A-to-I Human chr1 + 10080538 10080538 10080538 GTCCCTCAGAAAACTAAAAACAGAGCTACCATATGATCTGGCAGTCCCACTGAGTATATATCCAA GTCCCTCAGAAAACTAAAAACAGAGCTACCATGTGATCTGGCAGTCCCACTGAGTATATATCCAA A G UBE4B Ensembl:ENSG00000130939 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1212115641 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90073,RMVar_hsa_circ_128859,RMVar_hsa_circ_319612,RMVar_hsa_circ_353688,RMVar_hsa_circ_12294,RMVar_hsa_circ_128860 12671 RMVar_ID_12671 Human_SNP_ID_2783664 A-to-I Human chr1 + 10111834 10111834 10111834 CAAAAATTAGCTAGGCATGATGGCATGTGCCTATAATCCCAGCTACTAGAGAGGCTGAGGCAGGA CAAAAATTAGCTAGGCATGATGGCATGTGCCTGTAATCCCAGCTACTAGAGAGGCTGAGGCAGGA A G UBE4B Ensembl:ENSG00000130939 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223561980 Functional Loss SNV dbSNP153 33..33 33 - - - 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 12672 RMVar_ID_12672 Human_SNP_ID_2784315 A-to-I Human chr1 + 10114586 10114586 10114586 AATTAGTTGCTATAAAGACACAATAATTGGCCAGGTGCTGTGGCTCACACCTGTAATCCCAGCAC AATTAGTTGCTATAAAGACACAATAATTGGCCGGGTGCTGTGGCTCACACCTGTAATCCCAGCAC A G UBE4B Ensembl:ENSG00000130939 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1176319732 Functional Loss SNV dbSNP153 33..33 33 - - - 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 12673 RMVar_ID_12673 Human_SNP_ID_2784337 A-to-I Human chr1 + 10114685 10114684 10114685 CAGGAGTTTGAGACTATCCCGGCCAACATGGTAAAACACTGTCTCTACTAAAAATACAAAAATTA CAGGAGTTTGAGACTATCCCGGCCAACATGGT_AAACACTGTCTCTACTAAAAATACAAAAATTA TA T UBE4B Ensembl:ENSG00000130939 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1258478765 Functional Loss DEL dbSNP153 33..33 33 - - - 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 12674 RMVar_ID_12674 Human_SNP_ID_2784515 A-to-I Human chr1 + 10115337 10115337 10115337 TTGCCCAGGCTGGAGTGCAGTTGTGTGATCTCAGCTCACAGCAGCCTCTGCCTCCCGGGATTTAA TTGCCCAGGCTGGAGTGCAGTTGTGTGATCTCCGCTCACAGCAGCCTCTGCCTCCCGGGATTTAA A C UBE4B Ensembl:ENSG00000130939 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1394218813 Functional Loss SNV dbSNP153 33..33 33 - - - 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 12675 RMVar_ID_12675 Human_SNP_ID_2784525 A-to-I Human chr1 + 10115368 10115368 10115368 CAGCTCACAGCAGCCTCTGCCTCCCGGGATTTAAGAGATTCTCCTGCCTCAGCCTCCCAAGTAGC CAGCTCACAGCAGCCTCTGCCTCCCGGGATTTGAGAGATTCTCCTGCCTCAGCCTCCCAAGTAGC A G UBE4B Ensembl:ENSG00000130939 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270025014 Functional Loss SNV dbSNP153 33..33 33 - - - 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 12676 RMVar_ID_12676 Human_SNP_ID_2784557 A-to-I Human chr1 + 10115519 10115519 10115519 TCTCCAACTCCTATACCTCAAGTGATCCACCTACCTTAGCCTCCCAAAGTGCTGGGATTACAGGC TCTCCAACTCCTATACCTCAAGTGATCCACCTGCCTTAGCCTCCCAAAGTGCTGGGATTACAGGC A G UBE4B Ensembl:ENSG00000130939 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1260597797 Functional Loss SNV dbSNP153 33..33 33 - - - 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 12677 RMVar_ID_12677 Human_SNP_ID_2786771 A-to-I Human chr1 + 10124955 10124955 10124955 CGAGACCAGGCTGGGCAACATGGCAAAACCCCATCTCTACTCAAAATACAAAAAATTAGCTGGCG CGAGACCAGGCTGGGCAACATGGCAAAACCCCGTCTCTACTCAAAATACAAAAAATTAGCTGGCG A G UBE4B Ensembl:ENSG00000130939 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1360965625 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_436,RMVar_hsa_circ_90073,RMVar_hsa_circ_4601,RMVar_hsa_circ_128859,RMVar_hsa_circ_356658,RMVar_hsa_circ_18914,RMVar_hsa_circ_342817,RMVar_hsa_circ_128861,RMVar_hsa_circ_128864,RMVar_hsa_circ_330109,RMVar_hsa_circ_34341,RMVar_hsa_circ_128867,RMVar_hsa_circ_40282,RMVar_hsa_circ_373995,RMVar_hsa_circ_345359,RMVar_hsa_circ_343797,RMVar_hsa_circ_351489,RMVar_hsa_circ_303123,RMVar_hsa_circ_271842,RMVar_hsa_circ_281937,RMVar_hsa_circ_291142,RMVar_hsa_circ_278777,RMVar_hsa_circ_25726,RMVar_hsa_circ_267445,RMVar_hsa_circ_7080,RMVar_hsa_circ_44002,RMVar_hsa_circ_68860,RMVar_hsa_circ_128870,RMVar_hsa_circ_128872,RMVar_hsa_circ_128873,RMVar_hsa_circ_128871,RMVar_hsa_circ_321097,RMVar_hsa_circ_331100,RMVar_hsa_circ_311336,RMVar_hsa_circ_128875,RMVar_hsa_circ_30862,RMVar_hsa_circ_128874 12678 RMVar_ID_12678 Human_SNP_ID_2794745 A-to-I Human chr1 + 10156315 10156315 10156315 ACGCTAGAGTGTAGTGGTACAATTACAGCACCATGCACTCTTGACCTCCCGGGCTCAAGTGATCC ACGCTAGAGTGTAGTGGTACAATTACAGCACCGTGCACTCTTGACCTCCCGGGCTCAAGTGATCC A G UBE4B Ensembl:ENSG00000130939 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs554735358 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3625,RMVar_hsa_circ_90073,RMVar_hsa_circ_128859,RMVar_hsa_circ_128867,RMVar_hsa_circ_373995,RMVar_hsa_circ_343797,RMVar_hsa_circ_303123,RMVar_hsa_circ_267445,RMVar_hsa_circ_46870,RMVar_hsa_circ_325027,RMVar_hsa_circ_377580,RMVar_hsa_circ_44472,RMVar_hsa_circ_304451,RMVar_hsa_circ_128887,RMVar_hsa_circ_289183,RMVar_hsa_circ_274341,RMVar_hsa_circ_128888,RMVar_hsa_circ_128889,RMVar_hsa_circ_128893,RMVar_hsa_circ_302886,RMVar_hsa_circ_21826,RMVar_hsa_circ_278140,RMVar_hsa_circ_128896,RMVar_hsa_circ_128895,RMVar_hsa_circ_313944 12679 RMVar_ID_12679 Human_SNP_ID_2794777 A-to-I Human chr1 + 10156461 10156461 10156461 GGGGTTTCACGATGTTCACCAGGCTGGTCTCAAACTCCTGAGCTCAAGTGATCTGCCCACCCGGG GGGGTTTCACGATGTTCACCAGGCTGGTCTCAGACTCCTGAGCTCAAGTGATCTGCCCACCCGGG A G UBE4B Ensembl:ENSG00000130939 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1281663716 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3625,RMVar_hsa_circ_90073,RMVar_hsa_circ_128859,RMVar_hsa_circ_128867,RMVar_hsa_circ_373995,RMVar_hsa_circ_343797,RMVar_hsa_circ_303123,RMVar_hsa_circ_267445,RMVar_hsa_circ_46870,RMVar_hsa_circ_325027,RMVar_hsa_circ_377580,RMVar_hsa_circ_44472,RMVar_hsa_circ_304451,RMVar_hsa_circ_128887,RMVar_hsa_circ_289183,RMVar_hsa_circ_274341,RMVar_hsa_circ_128888,RMVar_hsa_circ_128889,RMVar_hsa_circ_128893,RMVar_hsa_circ_302886,RMVar_hsa_circ_21826,RMVar_hsa_circ_278140,RMVar_hsa_circ_128896,RMVar_hsa_circ_128895,RMVar_hsa_circ_313944 12680 RMVar_ID_12680 Human_SNP_ID_2794917 A-to-I Human chr1 + 10156997 10156997 10156997 TGAAACCAGCCTAGGCAACATAGTGAGACCCCATCTGTAAAAAAATTAAAAGTGAAAAAAAAAAT TGAAACCAGCCTAGGCAACATAGTGAGACCCCTTCTGTAAAAAAATTAAAAGTGAAAAAAAAAAT A T UBE4B Ensembl:ENSG00000130939 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs951896610 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3625,RMVar_hsa_circ_90073,RMVar_hsa_circ_128859,RMVar_hsa_circ_128867,RMVar_hsa_circ_373995,RMVar_hsa_circ_343797,RMVar_hsa_circ_303123,RMVar_hsa_circ_267445,RMVar_hsa_circ_46870,RMVar_hsa_circ_325027,RMVar_hsa_circ_377580,RMVar_hsa_circ_44472,RMVar_hsa_circ_304451,RMVar_hsa_circ_128887,RMVar_hsa_circ_289183,RMVar_hsa_circ_274341,RMVar_hsa_circ_128888,RMVar_hsa_circ_128889,RMVar_hsa_circ_128893,RMVar_hsa_circ_302886,RMVar_hsa_circ_21826,RMVar_hsa_circ_278140,RMVar_hsa_circ_128896,RMVar_hsa_circ_128895,RMVar_hsa_circ_313944 12681 RMVar_ID_12681 Human_SNP_ID_2795080 A-to-I Human chr1 + 10157670 10157670 10157670 CGTGGTGGCGCATGTCTATAGTCCCAGCTACTAGGGAGGCTGAGGCAGGAGAATTGCTTGAACCC CGTGGTGGCGCATGTCTATAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATTGCTTGAACCC A T UBE4B Ensembl:ENSG00000130939 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1476406222 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3625,RMVar_hsa_circ_90073,RMVar_hsa_circ_128859,RMVar_hsa_circ_128867,RMVar_hsa_circ_373995,RMVar_hsa_circ_343797,RMVar_hsa_circ_303123,RMVar_hsa_circ_267445,RMVar_hsa_circ_46870,RMVar_hsa_circ_325027,RMVar_hsa_circ_377580,RMVar_hsa_circ_44472,RMVar_hsa_circ_304451,RMVar_hsa_circ_128887,RMVar_hsa_circ_289183,RMVar_hsa_circ_274341,RMVar_hsa_circ_128888,RMVar_hsa_circ_128889,RMVar_hsa_circ_128893,RMVar_hsa_circ_302886,RMVar_hsa_circ_21826,RMVar_hsa_circ_278140,RMVar_hsa_circ_128896,RMVar_hsa_circ_128895,RMVar_hsa_circ_313944 12682 RMVar_ID_12682 Human_SNP_ID_2795085 A-to-I Human chr1 + 10157684 10157684 10157684 TCTATAGTCCCAGCTACTAGGGAGGCTGAGGCAGGAGAATTGCTTGAACCCCGAGGCAGAGGTTG TCTATAGTCCCAGCTACTAGGGAGGCTGAGGCGGGAGAATTGCTTGAACCCCGAGGCAGAGGTTG A G UBE4B Ensembl:ENSG00000130939 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971295840 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3625,RMVar_hsa_circ_90073,RMVar_hsa_circ_128859,RMVar_hsa_circ_128867,RMVar_hsa_circ_373995,RMVar_hsa_circ_343797,RMVar_hsa_circ_303123,RMVar_hsa_circ_267445,RMVar_hsa_circ_46870,RMVar_hsa_circ_325027,RMVar_hsa_circ_377580,RMVar_hsa_circ_44472,RMVar_hsa_circ_304451,RMVar_hsa_circ_128887,RMVar_hsa_circ_289183,RMVar_hsa_circ_274341,RMVar_hsa_circ_128888,RMVar_hsa_circ_128889,RMVar_hsa_circ_128893,RMVar_hsa_circ_302886,RMVar_hsa_circ_21826,RMVar_hsa_circ_278140,RMVar_hsa_circ_128896,RMVar_hsa_circ_128895,RMVar_hsa_circ_313944 12683 RMVar_ID_12683 Human_SNP_ID_2796383 A-to-I Human chr1 + 10163082 10163081 10163083 TTTGTTTTTTATTATTATTAATAAATAAAGACAGAGTGTTGATCTGTCGCCTTGGCTGGAGTGCA TTTGTTTTTTATTATTATTAATAAATAAAGAC__AGTGTTGATCTGTCGCCTTGGCTGGAGTGCA CAG C UBE4B Ensembl:ENSG00000130939 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1206668160 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_23302677 RMVar_hsa_circ_3625,RMVar_hsa_circ_90073,RMVar_hsa_circ_128859,RMVar_hsa_circ_303123,RMVar_hsa_circ_304451,RMVar_hsa_circ_21826,RMVar_hsa_circ_60127,RMVar_hsa_circ_55699,RMVar_hsa_circ_363345,RMVar_hsa_circ_320459,RMVar_hsa_circ_128897 12684 RMVar_ID_12684 Human_SNP_ID_2811223 A-to-I Human chr1 + 10214855 10214855 10214855 CACCCACCTCAGCCTCCCAAAGTGTTGGGATTACAGGCATGAGCTACTGCACCTGGGCTACCATT CACCCACCTCAGCCTCCCAAAGTGTTGGGATTGCAGGCATGAGCTACTGCACCTGGGCTACCATT A G KIF1B Ensembl:ENSG00000054523 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1028025316 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10496861 12685 RMVar_ID_12685 Human_SNP_ID_2820324 A-to-I Human chr1 + 10249640 10249640 10249640 AAATAGGCTCTTGGCTGGGTCCAGTGGCCCACACTTGTAATCCTAGCACTTTGGGAGGCCAAAAC AAATAGGCTCTTGGCTGGGTCCAGTGGCCCACGCTTGTAATCCTAGCACTTTGGGAGGCCAAAAC A G KIF1B Ensembl:ENSG00000054523 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1334374050 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57685,RMVar_hsa_circ_314301,RMVar_hsa_circ_339411,RMVar_hsa_circ_340514,RMVar_hsa_circ_346332,RMVar_hsa_circ_315964,RMVar_hsa_circ_289904,RMVar_hsa_circ_52418,RMVar_hsa_circ_55735,RMVar_hsa_circ_48398,RMVar_hsa_circ_128899,RMVar_hsa_circ_4505,RMVar_hsa_circ_18530,RMVar_hsa_circ_128901,RMVar_hsa_circ_128902,RMVar_hsa_circ_128903,RMVar_hsa_circ_128900,RMVar_hsa_circ_128898 12686 RMVar_ID_12686 Human_SNP_ID_2821803 A-to-I Human chr1 + 10255483 10255483 10255483 GTAGTGGTGGATGCCAGTAATCCCAGCTACTCAGGAGGCTGAGGCGGGAGAATTTCTTGAACCCG GTAGTGGTGGATGCCAGTAATCCCAGCTACTCGGGAGGCTGAGGCGGGAGAATTTCTTGAACCCG A G KIF1B Ensembl:ENSG00000054523 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1004108152 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57685,RMVar_hsa_circ_314301,RMVar_hsa_circ_339411,RMVar_hsa_circ_340514,RMVar_hsa_circ_346332,RMVar_hsa_circ_315964,RMVar_hsa_circ_289904,RMVar_hsa_circ_52418,RMVar_hsa_circ_55735,RMVar_hsa_circ_48398,RMVar_hsa_circ_128899,RMVar_hsa_circ_4505,RMVar_hsa_circ_18530,RMVar_hsa_circ_128901,RMVar_hsa_circ_128902,RMVar_hsa_circ_128903,RMVar_hsa_circ_128900,RMVar_hsa_circ_128898 12687 RMVar_ID_12687 Human_SNP_ID_2822339 A-to-I Human chr1 + 10257459 10257459 10257459 ATCGCACCACTGCACTCCAGCCTGGGTGATGGAACATGACTGTGTCTCAAAAAAAAAAAAAGGAA ATCGCACCACTGCACTCCAGCCTGGGTGATGGGACATGACTGTGTCTCAAAAAAAAAAAAAGGAA A G KIF1B Ensembl:ENSG00000054523 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs866781395 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1176,RMVar_hsa_circ_57685,RMVar_hsa_circ_314301,RMVar_hsa_circ_339411,RMVar_hsa_circ_340514,RMVar_hsa_circ_346332,RMVar_hsa_circ_289904,RMVar_hsa_circ_52418,RMVar_hsa_circ_55735,RMVar_hsa_circ_48398,RMVar_hsa_circ_128899,RMVar_hsa_circ_4505,RMVar_hsa_circ_18530,RMVar_hsa_circ_128901,RMVar_hsa_circ_128902,RMVar_hsa_circ_128903,RMVar_hsa_circ_128900,RMVar_hsa_circ_36253,RMVar_hsa_circ_309934,RMVar_hsa_circ_128898,RMVar_hsa_circ_328697,RMVar_hsa_circ_273074,RMVar_hsa_circ_10690,RMVar_hsa_circ_128904,RMVar_hsa_circ_128905,RMVar_hsa_circ_128906 12688 RMVar_ID_12688 Human_SNP_ID_2824308 A-to-I Human chr1 + 10265097 10265097 10265097 CTCAGTGATCGTCCTGCCTCAGCCTCCTGAGTAATTTGCACCACAGGCATGTGCCACAGTGTGTG CTCAGTGATCGTCCTGCCTCAGCCTCCTGAGTGATTTGCACCACAGGCATGTGCCACAGTGTGTG A G KIF1B Ensembl:ENSG00000054523 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232902183 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1176,RMVar_hsa_circ_339411,RMVar_hsa_circ_340514,RMVar_hsa_circ_346332,RMVar_hsa_circ_289904,RMVar_hsa_circ_52418,RMVar_hsa_circ_55735,RMVar_hsa_circ_48398,RMVar_hsa_circ_128899,RMVar_hsa_circ_4505,RMVar_hsa_circ_18530,RMVar_hsa_circ_128901,RMVar_hsa_circ_128900,RMVar_hsa_circ_36253,RMVar_hsa_circ_128898,RMVar_hsa_circ_328697,RMVar_hsa_circ_10690,RMVar_hsa_circ_128909,RMVar_hsa_circ_29058,RMVar_hsa_circ_268423,RMVar_hsa_circ_305871,RMVar_hsa_circ_128906,RMVar_hsa_circ_306914,RMVar_hsa_circ_344449,RMVar_hsa_circ_288526,RMVar_hsa_circ_272787,RMVar_hsa_circ_35562,RMVar_hsa_circ_66971,RMVar_hsa_circ_34926,RMVar_hsa_circ_128911,RMVar_hsa_circ_128913,RMVar_hsa_circ_128912,RMVar_hsa_circ_128910,RMVar_hsa_circ_33795,RMVar_hsa_circ_316883,RMVar_hsa_circ_128907,RMVar_hsa_circ_128908,RMVar_hsa_circ_335418,RMVar_hsa_circ_340188,RMVar_hsa_circ_377946,RMVar_hsa_circ_325694,RMVar_hsa_circ_302295,RMVar_hsa_circ_313257,RMVar_hsa_circ_287959,RMVar_hsa_circ_128919,RMVar_hsa_circ_128921,RMVar_hsa_circ_128922,RMVar_hsa_circ_128920,RMVar_hsa_circ_128917,RMVar_hsa_circ_128918,RMVar_hsa_circ_128916 12689 RMVar_ID_12689 Human_SNP_ID_2824809 A-to-I Human chr1 + 10267193 10267193 10267193 GGCATGTGCCACCACGCCTGGCTCCTTTTTGTATTTTTGGTAGAGACGGGATTTCACCATGTTGG GGCATGTGCCACCACGCCTGGCTCCTTTTTGTGTTTTTGGTAGAGACGGGATTTCACCATGTTGG A G KIF1B Ensembl:ENSG00000054523 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs982689865 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1176,RMVar_hsa_circ_339411,RMVar_hsa_circ_340514,RMVar_hsa_circ_346332,RMVar_hsa_circ_289904,RMVar_hsa_circ_52418,RMVar_hsa_circ_55735,RMVar_hsa_circ_48398,RMVar_hsa_circ_128899,RMVar_hsa_circ_4505,RMVar_hsa_circ_18530,RMVar_hsa_circ_128901,RMVar_hsa_circ_128900,RMVar_hsa_circ_36253,RMVar_hsa_circ_128898,RMVar_hsa_circ_328697,RMVar_hsa_circ_10690,RMVar_hsa_circ_128909,RMVar_hsa_circ_29058,RMVar_hsa_circ_268423,RMVar_hsa_circ_305871,RMVar_hsa_circ_128906,RMVar_hsa_circ_306914,RMVar_hsa_circ_344449,RMVar_hsa_circ_288526,RMVar_hsa_circ_272787,RMVar_hsa_circ_35562,RMVar_hsa_circ_66971,RMVar_hsa_circ_34926,RMVar_hsa_circ_128911,RMVar_hsa_circ_128913,RMVar_hsa_circ_128912,RMVar_hsa_circ_128910,RMVar_hsa_circ_33795,RMVar_hsa_circ_316883,RMVar_hsa_circ_128907,RMVar_hsa_circ_128908,RMVar_hsa_circ_335418,RMVar_hsa_circ_340188,RMVar_hsa_circ_377946,RMVar_hsa_circ_325694,RMVar_hsa_circ_302295,RMVar_hsa_circ_313257,RMVar_hsa_circ_287959,RMVar_hsa_circ_128919,RMVar_hsa_circ_128921,RMVar_hsa_circ_128922,RMVar_hsa_circ_128920,RMVar_hsa_circ_128917,RMVar_hsa_circ_128918,RMVar_hsa_circ_128916 12690 RMVar_ID_12690 Human_SNP_ID_2830505 A-to-I Human chr1 + 10290501 10290501 10290501 TTGGGAACTTTATTCTTTTTTTTCTTTTTTTGAGATGGAGTTTTGCTCTGTTGCTCAGGCTGCAG TTGGGAACTTTATTCTTTTTTTTCTTTTTTTGCGATGGAGTTTTGCTCTGTTGCTCAGGCTGCAG A C KIF1B Ensembl:ENSG00000054523 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886520444 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_354,RMVar_hsa_circ_340514,RMVar_hsa_circ_52418,RMVar_hsa_circ_55735,RMVar_hsa_circ_48398,RMVar_hsa_circ_128899,RMVar_hsa_circ_4505,RMVar_hsa_circ_128898,RMVar_hsa_circ_10690,RMVar_hsa_circ_268423,RMVar_hsa_circ_35562,RMVar_hsa_circ_66971,RMVar_hsa_circ_34926,RMVar_hsa_circ_74707,RMVar_hsa_circ_33795,RMVar_hsa_circ_128907,RMVar_hsa_circ_128908,RMVar_hsa_circ_340188,RMVar_hsa_circ_377946,RMVar_hsa_circ_325694,RMVar_hsa_circ_128917,RMVar_hsa_circ_128916,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_297898,RMVar_hsa_circ_319336,RMVar_hsa_circ_268567,RMVar_hsa_circ_22365,RMVar_hsa_circ_52634,RMVar_hsa_circ_10984,RMVar_hsa_circ_869,RMVar_hsa_circ_128935,RMVar_hsa_circ_128937,RMVar_hsa_circ_128939,RMVar_hsa_circ_128938,RMVar_hsa_circ_128936,RMVar_hsa_circ_118172,RMVar_hsa_circ_42061,RMVar_hsa_circ_315178,RMVar_hsa_circ_339750,RMVar_hsa_circ_128942,RMVar_hsa_circ_346490,RMVar_hsa_circ_338124,RMVar_hsa_circ_314800,RMVar_hsa_circ_58805,RMVar_hsa_circ_128944,RMVar_hsa_circ_128945,RMVar_hsa_circ_128946,RMVar_hsa_circ_128943,RMVar_hsa_circ_331306,RMVar_hsa_circ_32212 12691 RMVar_ID_12691 Human_SNP_ID_2831525 A-to-I Human chr1 + 10294757 10294757 10294757 AGGCGTGGTGGCGAACACCTGTAATCCCAGCTACTTGAGAGGCTGAGGCAGGAGAATCACTTGAA AGGCGTGGTGGCGAACACCTGTAATCCCAGCTGCTTGAGAGGCTGAGGCAGGAGAATCACTTGAA A G KIF1B Ensembl:ENSG00000054523 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1319993258 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_354,RMVar_hsa_circ_340514,RMVar_hsa_circ_52418,RMVar_hsa_circ_55735,RMVar_hsa_circ_128899,RMVar_hsa_circ_4505,RMVar_hsa_circ_128898,RMVar_hsa_circ_10690,RMVar_hsa_circ_268423,RMVar_hsa_circ_66971,RMVar_hsa_circ_34926,RMVar_hsa_circ_33795,RMVar_hsa_circ_128907,RMVar_hsa_circ_340188,RMVar_hsa_circ_128916,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_319336,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_128938,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_314800,RMVar_hsa_circ_8455,RMVar_hsa_circ_58805,RMVar_hsa_circ_128944,RMVar_hsa_circ_128945,RMVar_hsa_circ_128943,RMVar_hsa_circ_331306,RMVar_hsa_circ_53937,RMVar_hsa_circ_325288,RMVar_hsa_circ_334798,RMVar_hsa_circ_287473,RMVar_hsa_circ_128948,RMVar_hsa_circ_22360,RMVar_hsa_circ_307821,RMVar_hsa_circ_128947,RMVar_hsa_circ_290613,RMVar_hsa_circ_128949 12692 RMVar_ID_12692 Human_SNP_ID_2835981 A-to-I Human chr1 + 10313165 10313165 10313165 TTGGCTCACTGCAACCTCTGCTGCCCTGGTTCAAGCGATTCTTGTGGCTCAGCCTCCCAAGTAGC TTGGCTCACTGCAACCTCTGCTGCCCTGGTTCGAGCGATTCTTGTGGCTCAGCCTCCCAAGTAGC A G KIF1B Ensembl:ENSG00000054523 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs901973095 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_52418,RMVar_hsa_circ_4505,RMVar_hsa_circ_128898,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 12693 RMVar_ID_12693 Human_SNP_ID_2846542 A-to-I Human chr1 + 10356881 10356881 10356881 AAGATCGTGCCACTACACTCCAGCCTGGCGACAGAGCTAGACTCCGTCTCTAAATAAATAAATAA AAGATCGTGCCACTACACTCCAGCCTGGCGACGGAGCTAGACTCCGTCTCTAAATAAATAAATAA A G KIF1B Ensembl:ENSG00000054523 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1356168327 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1562,RMVar_hsa_circ_128954,RMVar_hsa_circ_6417,RMVar_hsa_circ_1629,RMVar_hsa_circ_357406,RMVar_hsa_circ_266934,RMVar_hsa_circ_312306,RMVar_hsa_circ_331163,RMVar_hsa_circ_54197,RMVar_hsa_circ_25153,RMVar_hsa_circ_11936,RMVar_hsa_circ_330528,RMVar_hsa_circ_6180,RMVar_hsa_circ_265623,RMVar_hsa_circ_59557,RMVar_hsa_circ_128965,RMVar_hsa_circ_128966,RMVar_hsa_circ_34774,RMVar_hsa_circ_370095,RMVar_hsa_circ_128969,RMVar_hsa_circ_21136,RMVar_hsa_circ_21757,RMVar_hsa_circ_11489 12694 RMVar_ID_12694 Human_SNP_ID_2850490 A-to-I Human chr1 + 10372557 10372557 10372557 GAAATCAGCCAGGCATAGGGGCATGTACCTGTAATCCCAGCTACTGGGGAGGCTGAGGCAGGAAG GAAATCAGCCAGGCATAGGGGCATGTACCTGTGATCCCAGCTACTGGGGAGGCTGAGGCAGGAAG A G KIF1B Ensembl:ENSG00000054523 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1423195761 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128954,RMVar_hsa_circ_6417,RMVar_hsa_circ_1629,RMVar_hsa_circ_312306,RMVar_hsa_circ_370095,RMVar_hsa_circ_57070,RMVar_hsa_circ_128969,RMVar_hsa_circ_301147,RMVar_hsa_circ_362780,RMVar_hsa_circ_128977,RMVar_hsa_circ_128978,RMVar_hsa_circ_287839,RMVar_hsa_circ_121077,RMVar_hsa_circ_128981,RMVar_hsa_circ_128980,RMVar_hsa_circ_355134,RMVar_hsa_circ_128985,RMVar_hsa_circ_128987,RMVar_hsa_circ_103765,RMVar_hsa_circ_128989,RMVar_hsa_circ_295207 12695 RMVar_ID_12695 Human_SNP_ID_2851965 A-to-I Human chr1 + 10377789 10377789 10377789 TGAAACCCCGTCTCTACTAAAAATACAAAATTAGTCGGGTATGGTGGCACATGCCTGTAATTCCA TGAAACCCCGTCTCTACTAAAAATACAAAATTCGTCGGGTATGGTGGCACATGCCTGTAATTCCA A C KIF1B Ensembl:ENSG00000054523 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1467592451 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121077,RMVar_hsa_circ_128980 12696 RMVar_ID_12696 Human_SNP_ID_2852639 A-to-I Human chr1 + 10380585 10380585 10380585 AAAAGTAGCCAGGCGTGGTGGCGTGTGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA AAAAGTAGCCAGGCGTGGTGGCGTGTGCCTGTGGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA A G KIF1B Ensembl:ENSG00000054523 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1214417320 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121077,RMVar_hsa_circ_128980 12697 RMVar_ID_12697 Human_SNP_ID_2852640 A-to-I Human chr1 + 10380585 10380585 10380585 AAAAGTAGCCAGGCGTGGTGGCGTGTGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA AAAAGTAGCCAGGCGTGGTGGCGTGTGCCTGTTGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA A T KIF1B Ensembl:ENSG00000054523 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1214417320 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121077,RMVar_hsa_circ_128980 12698 RMVar_ID_12698 Human_SNP_ID_2853133 A-to-I Human chr1 + 10382636 10382636 10382636 GGGGTTTCAGCACATTGGCCAGACTGGTCTCAAACTCCTGACCTCAGGTGATCCGCCCACCTCGG GGGGTTTCAGCACATTGGCCAGACTGGTCTCAGACTCCTGACCTCAGGTGATCCGCCCACCTCGG A G - - Other Unknown GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs927143632 Functional Loss SNV dbSNP153 33..33 33 - - - 12699 RMVar_ID_12699 Human_SNP_ID_2856824 A-to-I Human chr1 + 10396907 10396907 10396907 AGATCGTGCCACTGCACTCTAGCTTGGGCTACAGAGTGAGACTCCATCTCACACACACACACACA AGATCGTGCCACTGCACTCTAGCTTGGGCTACGGAGTGAGACTCCATCTCACACACACACACACA A G AL139424.2 Ensembl:ENSG00000284642 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1426835528 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_16132 12700 RMVar_ID_12700 Human_SNP_ID_2858115 A-to-I Human chr1 + 10401058 10401058 10401058 GAAACCCCGTCTCTACTAAAAATATAAAAATTAGCTGGGCTTTGTGGCTCATGCCTGTAATCCCA GAAACCCCGTCTCTACTAAAAATATAAAAATTCGCTGGGCTTTGTGGCTCATGCCTGTAATCCCA A C PGD Ensembl:ENSG00000142657 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs746050616 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76698,RMVar_hsa_circ_87015,RMVar_hsa_circ_122920,RMVar_hsa_circ_119044,RMVar_hsa_circ_128995,RMVar_hsa_circ_128996,RMVar_hsa_circ_128997,RMVar_hsa_circ_128998 12701 RMVar_ID_12701 Human_SNP_ID_2858583 A-to-I Human chr1 + 10402708 10402708 10402708 ACAACGCCCGGCTAATTTTTCGTATTTTTAGTAGAGACGAGGTTTCACCATGTTAGCCAGGATGG ACAACGCCCGGCTAATTTTTCGTATTTTTAGTGGAGACGAGGTTTCACCATGTTAGCCAGGATGG A G PGD Ensembl:ENSG00000142657 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1486632859 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76698,RMVar_hsa_circ_87015,RMVar_hsa_circ_122920,RMVar_hsa_circ_119044,RMVar_hsa_circ_128995,RMVar_hsa_circ_128996,RMVar_hsa_circ_128997,RMVar_hsa_circ_128998 12702 RMVar_ID_12702 Human_SNP_ID_2859903 A-to-I Human chr1 + 10407190 10407190 10407190 AAAAAATTAGCCAGGCATGGTGGCTCACGCCTATGGTCCCAGCACTTTGGGAAGCTGAGGTGTGA AAAAAATTAGCCAGGCATGGTGGCTCACGCCTGTGGTCCCAGCACTTTGGGAAGCTGAGGTGTGA A G PGD Ensembl:ENSG00000142657 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs751109178 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26753232 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_273143,RMVar_hsa_circ_61009,RMVar_hsa_circ_39853,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 12703 RMVar_ID_12703 Human_SNP_ID_2860629 A-to-I Human chr1 + 10409930 10409930 10409930 GGCCCACCTTGGCCTCCCAAAGTGTTGGGATTATAGGCGTGAGCCACCGCACCCAGCCTGCAACT GGCCCACCTTGGCCTCCCAAAGTGTTGGGATTGTAGGCGTGAGCCACCGCACCCAGCCTGCAACT A G PGD Ensembl:ENSG00000142657 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1365653230 Functional Loss SNV dbSNP153 33..33 33 - - - 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_129005,RMVar_hsa_circ_37014 12704 RMVar_ID_12704 Human_SNP_ID_2861845 A-to-I Human chr1 + 10414579 10414579 10414579 GTGTGTTATTAGTGGAGACGGGGTTTTACCATATTGGTCAGGCTGGTCTCGAACTCCTAACCTCA GTGTGTTATTAGTGGAGACGGGGTTTTACCATCTTGGTCAGGCTGGTCTCGAACTCCTAACCTCA A C PGD Ensembl:ENSG00000142657 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1375223744 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76698,RMVar_hsa_circ_36426,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_39853,RMVar_hsa_circ_129001,RMVar_hsa_circ_361699,RMVar_hsa_circ_90592,RMVar_hsa_circ_129004,RMVar_hsa_circ_351502,RMVar_hsa_circ_88420,RMVar_hsa_circ_122759,RMVar_hsa_circ_129005,RMVar_hsa_circ_37014,RMVar_hsa_circ_340027,RMVar_hsa_circ_377350,RMVar_hsa_circ_129007,RMVar_hsa_circ_129008,RMVar_hsa_circ_75897 12705 RMVar_ID_12705 Human_SNP_ID_2869530 A-to-I Human chr1 - 10440380 10440380 10440380 AGTGAATTACTCCTCCTGGCTAAGAGCTTCACATCTTCAGTGTTAATTGTGGTTCTTTTCGCATG AGTGAATTACTCCTCCTGGCTAAGAGCTTCACTTCTTCAGTGTTAATTGTGGTTCTTTTCGCATG T A - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs751031592 Functional Loss SNV dbSNP153 33..33 33 - - - 12706 RMVar_ID_12706 Human_SNP_ID_2871293 A-to-I Human chr1 - 10446764 10446764 10446764 GTGGAGGCACATACCTGTGGTCTCAGCTACTTAGGGGGCTGAGGTAGGAGGATCACCTGAGCATG GTGGAGGCACATACCTGTGGTCTCAGCTACTTGGGGGGCTGAGGTAGGAGGATCACCTGAGCATG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350612702 Functional Loss SNV dbSNP153 33..33 33 - - - 12707 RMVar_ID_12707 Human_SNP_ID_2873983 A-to-I Human chr1 - 10456106 10456106 10456106 CTTCACTCTTTTTCTTTTCTTTTTTTAAGACAATCTCGCTCTGTCACCCAGGCTGGAGTTCAGTG CTTCACTCTTTTTCTTTTCTTTTTTTAAGACAGTCTCGCTCTGTCACCCAGGCTGGAGTTCAGTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs902149993 Functional Loss SNV dbSNP153 33..33 33 - - - 12708 RMVar_ID_12708 Human_SNP_ID_2874269 A-to-I Human chr1 - 10457233 10457233 10457233 GGGAGGCTAAGGCAGAAGGATCACTTGAGCCCAGGAGTTCGAGGCTACAATGAGCTGTGATCGTG GGGAGGCTAAGGCAGAAGGATCACTTGAGCCCGGGAGTTCGAGGCTACAATGAGCTGTGATCGTG T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs182502766 Functional Loss SNV dbSNP153 33..33 33 - - - 12709 RMVar_ID_12709 Human_SNP_ID_2874272 A-to-I Human chr1 - 10457243 10457243 10457243 CTAGATACTCGGGAGGCTAAGGCAGAAGGATCACTTGAGCCCAGGAGTTCGAGGCTACAATGAGC CTAGATACTCGGGAGGCTAAGGCAGAAGGATCGCTTGAGCCCAGGAGTTCGAGGCTACAATGAGC T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE38233;GSE100210;GSE112787;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;293 Flip-In T-REx cells,empty vector;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,29967493,31158229 RNA-Seq:(High) rs1257163679 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5663970,Human_RBP_ID_26364795 12710 RMVar_ID_12710 Human_SNP_ID_2874290 A-to-I Human chr1 - 10457295 10457295 10457295 AAAAATGTAAAAAATAAAAATTAGCCGGGTGTAGTGGTACATGCCTGTAATCCTAGATACTCGGG AAAAATGTAAAAAATAAAAATTAGCCGGGTGTGGTGGTACATGCCTGTAATCCTAGATACTCGGG T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE38233;GSE100210;GSE112787;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;293 Flip-In T-REx cells,empty vector;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,29967493,31158229 RNA-Seq:(High) rs1476847623 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3275095,Human_RBP_ID_5663971,Human_RBP_ID_8279591,Human_RBP_ID_10500184,Human_RBP_ID_18213965 12711 RMVar_ID_12711 Human_SNP_ID_2874342 A-to-I Human chr1 - 10457455 10457455 10457455 TTGGCTAGACTGGTCTCAAACTCCTGACCTCAAGTGATCCACCTGCCTTGGCCTCCCAAAGTGCT TTGGCTAGACTGGTCTCAAACTCCTGACCTCAGGTGATCCACCTGCCTTGGCCTCCCAAAGTGCT T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,31158229,31158229,31158229 RNA-Seq:(High) rs1407007003 Functional Loss SNV dbSNP153 33..33 33 - - - 12712 RMVar_ID_12712 Human_SNP_ID_2874348 A-to-I Human chr1 - 10457490 10457490 10457490 TTTGGTATTTTTAGTAGACACAGGGTTTCACCATGTTGGCTAGACTGGTCTCAAACTCCTGACCT TTTGGTATTTTTAGTAGACACAGGGTTTCACCTTGTTGGCTAGACTGGTCTCAAACTCCTGACCT T A DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs776411430 Functional Loss SNV dbSNP153 33..33 33 - - - 12713 RMVar_ID_12713 Human_SNP_ID_2874356 A-to-I Human chr1 - 10457507 10457507 10457507 CACCCGGCTAAGTTTTTTTTGGTATTTTTAGTAGACACAGGGTTTCACCATGTTGGCTAGACTGG CACCCGGCTAAGTTTTTTTTGGTATTTTTAGTGGACACAGGGTTTCACCATGTTGGCTAGACTGG T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs1291219833 Functional Loss SNV dbSNP153 33..33 33 - - - 12714 RMVar_ID_12714 Human_SNP_ID_2874372 A-to-I Human chr1 - 10457556 10457556 10457556 CTCTTGCCTCAGCCTCCAGAGTAGCTGGGATTACAGGTGCCCGCCACCACACCCGGCTAAGTTTT CTCTTGCCTCAGCCTCCAGAGTAGCTGGGATTGCAGGTGCCCGCCACCACACCCGGCTAAGTTTT T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1172510059 Functional Loss SNV dbSNP153 33..33 33 - - - 12715 RMVar_ID_12715 Human_SNP_ID_2874382 A-to-I Human chr1 - 10457596 10457596 10457596 TCTGCTCACTGCAACCTCCATCTCCCAGGTTCAGGCGATTCTCTTGCCTCAGCCTCCAGAGTAGC TCTGCTCACTGCAACCTCCATCTCCCAGGTTCGGGCGATTCTCTTGCCTCAGCCTCCAGAGTAGC T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,31158229,31158229,31158229 RNA-Seq:(High) rs1355351342 Functional Loss SNV dbSNP153 33..33 33 - - - 12716 RMVar_ID_12716 Human_SNP_ID_2874390 A-to-I Human chr1 - 10457631 10457631 10457631 CTCTGTTGCCCAGGCTGGAGTGTAGTGGCACAATCTCTGCTCACTGCAACCTCCATCTCCCAGGT CTCTGTTGCCCAGGCTGGAGTGTAGTGGCACAGTCTCTGCTCACTGCAACCTCCATCTCCCAGGT T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1190826705 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26364798 12717 RMVar_ID_12717 Human_SNP_ID_2874471 A-to-I Human chr1 - 10457935 10457935 10457935 CATCAGCTTCCCAGAATTTTGGGATTACAGGCATGAGCCACCACACCCAGCCAGAATATTTTATT CATCAGCTTCCCAGAATTTTGGGATTACAGGCTTGAGCCACCACACCCAGCCAGAATATTTTATT T A DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE100210;GSE112787 HepG2 cell line;293 Flip-In T-REx cells,empty vector - 29129909,29967493 RNA-Seq:(High) rs1009070957 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23143006 12718 RMVar_ID_12718 Human_SNP_ID_2874472 A-to-I Human chr1 - 10457939 10457939 10457939 CCCACATCAGCTTCCCAGAATTTTGGGATTACAGGCATGAGCCACCACACCCAGCCAGAATATTT CCCACATCAGCTTCCCAGAATTTTGGGATTACGGGCATGAGCCACCACACCCAGCCAGAATATTT T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1325411484 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23143006 Human_miRNA_ID_604148,Human_miRNA_ID_1398308 12719 RMVar_ID_12719 Human_SNP_ID_2874480 A-to-I Human chr1 - 10457980 10457980 10457980 TTACCCAGGCTGGTCTCAAACTCCAGGCCTCAAGCAATCCTCCCACATCAGCTTCCCAGAATTTT TTACCCAGGCTGGTCTCAAACTCCAGGCCTCAGGCAATCCTCCCACATCAGCTTCCCAGAATTTT T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE100210;GSE112787;GSE107867 HepG2 cell line;293 Flip-In T-REx cells,empty vector;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 29129909,29967493,30559470 RNA-Seq:(High) rs529753972 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557599,Human_RBP_ID_26364803 12720 RMVar_ID_12720 Human_SNP_ID_2874483 A-to-I Human chr1 - 10457995 10457984 10457995 TTAAAACTCACCATGTTACCCAGGCTGGTCTCAAACTCCAGGCCTCAAGCAATCCTCCCACATCA TTAAAACTCACCATGTTACCCAGGCTGGTCTC___________CTCAAGCAATCCTCCCACATCA GGCCTGGAGTTT G DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335182158 Functional Loss DEL dbSNP153 33..43 33 - - - Human_RBP_ID_10500204,Human_RBP_ID_17557599,Human_RBP_ID_22778743,Human_RBP_ID_26364803 12721 RMVar_ID_12721 Human_SNP_ID_2874487 A-to-I Human chr1 - 10458010 10458010 10458010 GAAATCCAGGGTACATTAAAACTCACCATGTTACCCAGGCTGGTCTCAAACTCCAGGCCTCAAGC GAAATCCAGGGTACATTAAAACTCACCATGTTGCCCAGGCTGGTCTCAAACTCCAGGCCTCAAGC T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1012952835 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8279595,Human_RBP_ID_17328928,Human_RBP_ID_17444350,Human_RBP_ID_17557599,Human_RBP_ID_17719849 12722 RMVar_ID_12722 Human_SNP_ID_2874489 A-to-I Human chr1 - 10458015 10458015 10458015 CCTAGGAAATCCAGGGTACATTAAAACTCACCATGTTACCCAGGCTGGTCTCAAACTCCAGGCCT CCTAGGAAATCCAGGGTACATTAAAACTCACCGTGTTACCCAGGCTGGTCTCAAACTCCAGGCCT T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs777829896 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_969505,Human_RBP_ID_8279595,Human_RBP_ID_17210861,Human_RBP_ID_17328928,Human_RBP_ID_17444350,Human_RBP_ID_17557599,Human_RBP_ID_17674344,Human_RBP_ID_17719849,Human_RBP_ID_18213971 12723 RMVar_ID_12723 Human_SNP_ID_2874494 A-to-I Human chr1 - 10458044 10458044 10458044 CTGTCCTTGATTTACAGAGTAGCTACATTCCTAGGAAATCCAGGGTACATTAAAACTCACCATGT CTGTCCTTGATTTACAGAGTAGCTACATTCCTCGGAAATCCAGGGTACATTAAAACTCACCATGT T G DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE100210;GSE112787 HepG2 cell line;293 Flip-In T-REx cells,empty vector - 29129909,29967493 RNA-Seq:(High) rs1395926605 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_319397,Human_RBP_ID_17328928,Human_RBP_ID_17557599,Human_RBP_ID_17762321,Human_RBP_ID_18213972 12724 RMVar_ID_12724 Human_SNP_ID_2874688 A-to-I Human chr1 - 10458699 10458699 10458699 AACCCAGTCTACTAAAAATACAAAAATTAGCCAGGCGTGATGGTGGGCACCTGTAATCCCAGCTA AACCCAGTCTACTAAAAATACAAAAATTAGCCGGGCGTGATGGTGGGCACCTGTAATCCCAGCTA T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs1430201739 Functional Loss SNV dbSNP153 33..33 33 - - - 12725 RMVar_ID_12725 Human_SNP_ID_2874692 A-to-I Human chr1 - 10458730 10458730 10458730 GAGTTTGAGACCAGCCTGGCCAACGTGACAAAACCCAGTCTACTAAAAATACAAAAATTAGCCAG GAGTTTGAGACCAGCCTGGCCAACGTGACAAAGCCCAGTCTACTAAAAATACAAAAATTAGCCAG T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1279752059 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_319407 12726 RMVar_ID_12726 Human_SNP_ID_2874697 A-to-I Human chr1 - 10458740 10458740 10458740 CTGAGGTCAGGAGTTTGAGACCAGCCTGGCCAACGTGACAAAACCCAGTCTACTAAAAATACAAA CTGAGGTCAGGAGTTTGAGACCAGCCTGGCCAGCGTGACAAAACCCAGTCTACTAAAAATACAAA T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1190502851 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_319407 12727 RMVar_ID_12727 Human_SNP_ID_2874717 A-to-I Human chr1 - 10458810 10458810 10458810 ACAATAGGCCGGGCGCAGTGGCTCACACCTGCAGTCCCAGCACTTTGGGAGGCCAAGGCAGATGG ACAATAGGCCGGGCGCAGTGGCTCACACCTGCCGTCCCAGCACTTTGGGAGGCCAAGGCAGATGG T G DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984940008 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10500235 12728 RMVar_ID_12728 Human_SNP_ID_2874721 A-to-I Human chr1 - 10458818 10458818 10458818 AATATGTCACAATAGGCCGGGCGCAGTGGCTCACACCTGCAGTCCCAGCACTTTGGGAGGCCAAG AATATGTCACAATAGGCCGGGCGCAGTGGCTCGCACCTGCAGTCCCAGCACTTTGGGAGGCCAAG T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs976329014 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8953228,Human_RBP_ID_10500235 12729 RMVar_ID_12729 Human_SNP_ID_2874724 A-to-I Human chr1 - 10458826 10458826 10458826 AATATCACAATATGTCACAATAGGCCGGGCGCAGTGGCTCACACCTGCAGTCCCAGCACTTTGGG AATATCACAATATGTCACAATAGGCCGGGCGCGGTGGCTCACACCTGCAGTCCCAGCACTTTGGG T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs929475125 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8953228,Human_RBP_ID_10500235,Human_RBP_ID_17210868,Human_RBP_ID_18213983,Human_RBP_ID_26385190 12730 RMVar_ID_12730 Human_SNP_ID_2874799 A-to-I Human chr1 - 10459062 10459062 10459062 ATCACCTGAGGTCAGGAGTTCGAGACCAGCCTAGCCAACATGGTGAAACCCCGTCTCTACTGAAA ATCACCTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCCGTCTCTACTGAAA T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE100210;GSE112787;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;293 Flip-In T-REx cells,empty vector;Bronchiolar epithelium,BEP2D cell line - 29129909,29967493,31158229 RNA-Seq:(High) rs960050992 Functional Loss SNV dbSNP153 33..33 33 - - - 12731 RMVar_ID_12731 Human_SNP_ID_2874819 A-to-I Human chr1 - 10459126 10459126 10459126 CAATAGGCCGGGCGCAGTGGCTCACACCTGTAATCCCAGCATTTTGGGAGGCCAAGGTGGGCGGA CAATAGGCCGGGCGCAGTGGCTCACACCTGTAGTCCCAGCATTTTGGGAGGCCAAGGTGGGCGGA T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1141444 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1354831 12732 RMVar_ID_12732 Human_SNP_ID_2874824 A-to-I Human chr1 - 10459143 10459143 10459143 TAAGTAAAGAAATATCACAATAGGCCGGGCGCAGTGGCTCACACCTGTAATCCCAGCATTTTGGG TAAGTAAAGAAATATCACAATAGGCCGGGCGCGGTGGCTCACACCTGTAATCCCAGCATTTTGGG T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1038930786 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5664013,Human_RBP_ID_8240020,Human_RBP_ID_10500245,Human_RBP_ID_17210870,Human_RBP_ID_17328931,Human_RBP_ID_17444355,Human_RBP_ID_17765873 Human_miRNA_ID_1354831 12733 RMVar_ID_12733 Human_SNP_ID_2874825 A-to-I Human chr1 - 10459143 10459143 10459143 TAAGTAAAGAAATATCACAATAGGCCGGGCGCAGTGGCTCACACCTGTAATCCCAGCATTTTGGG TAAGTAAAGAAATATCACAATAGGCCGGGCGCCGTGGCTCACACCTGTAATCCCAGCATTTTGGG T G DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1038930786 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5664013,Human_RBP_ID_8240020,Human_RBP_ID_10500245,Human_RBP_ID_17210870,Human_RBP_ID_17328931,Human_RBP_ID_17444355,Human_RBP_ID_17765873 Human_miRNA_ID_1354831 12734 RMVar_ID_12734 Human_SNP_ID_2874991 A-to-I Human chr1 - 10459830 10459830 10459830 CTGACCTATAATCCTAGCTACTCTGGAGGCTAAGGCGAGAGTATCACTTGAGCCCAGGAGCTCAA CTGACCTATAATCCTAGCTACTCTGGAGGCTAGGGCGAGAGTATCACTTGAGCCCAGGAGCTCAA T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1321937329 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5664037,Human_RBP_ID_10500275,Human_RBP_ID_17558252,Human_RBP_ID_22369372,Human_RBP_ID_23143028,Human_RBP_ID_26364831 12735 RMVar_ID_12735 Human_SNP_ID_2874992 A-to-I Human chr1 - 10459831 10459831 10459831 ACTGACCTATAATCCTAGCTACTCTGGAGGCTAAGGCGAGAGTATCACTTGAGCCCAGGAGCTCA ACTGACCTATAATCCTAGCTACTCTGGAGGCTGAGGCGAGAGTATCACTTGAGCCCAGGAGCTCA T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE38233;GSE112787;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;293 Flip-In T-REx cells,empty vector;Bronchiolar epithelium,BEP2D cell line - 24183664,29967493,31158229 RNA-Seq:(High) rs1243703534 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5664037,Human_RBP_ID_10500275,Human_RBP_ID_17558252,Human_RBP_ID_19159750,Human_RBP_ID_22369372,Human_RBP_ID_23143028,Human_RBP_ID_26364831 12736 RMVar_ID_12736 Human_SNP_ID_2874998 A-to-I Human chr1 - 10459853 10459853 10459853 TAAGTTAGCCAGGCATGGTGGCACTGACCTATAATCCTAGCTACTCTGGAGGCTAAGGCGAGAGT TAAGTTAGCCAGGCATGGTGGCACTGACCTATGATCCTAGCTACTCTGGAGGCTAAGGCGAGAGT T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1276009308 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224334,Human_RBP_ID_1148456,Human_RBP_ID_3979301,Human_RBP_ID_5664037,Human_RBP_ID_10500276,Human_RBP_ID_17558252,Human_RBP_ID_18213997,Human_RBP_ID_23143028,Human_RBP_ID_26364831,Human_RBP_ID_27385195 12737 RMVar_ID_12737 Human_SNP_ID_2874999 A-to-I Human chr1 - 10459855 10459855 10459855 TTTAAGTTAGCCAGGCATGGTGGCACTGACCTATAATCCTAGCTACTCTGGAGGCTAAGGCGAGA TTTAAGTTAGCCAGGCATGGTGGCACTGACCTGTAATCCTAGCTACTCTGGAGGCTAAGGCGAGA T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE38233;GSE100210;GSE112787;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;293 Flip-In T-REx cells,empty vector;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,29967493,31158229,31158229 RNA-Seq:(High) rs1483036590 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224334,Human_RBP_ID_319424,Human_RBP_ID_1148456,Human_RBP_ID_5664037,Human_RBP_ID_10500278,Human_RBP_ID_17558252,Human_RBP_ID_18213997,Human_RBP_ID_23143028,Human_RBP_ID_26364831,Human_RBP_ID_27385195 12738 RMVar_ID_12738 Human_SNP_ID_2875004 A-to-I Human chr1 - 10459879 10459879 10459879 GACCCTGTCTCTACAAAAAAAAAATTTAAGTTAGCCAGGCATGGTGGCACTGACCTATAATCCTA GACCCTGTCTCTACAAAAAAAAAATTTAAGTTTGCCAGGCATGGTGGCACTGACCTATAATCCTA T A DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1026360840 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_319424,Human_RBP_ID_1148456,Human_RBP_ID_5664037,Human_RBP_ID_10500279,Human_RBP_ID_17558252,Human_RBP_ID_26385195,Human_RBP_ID_27385196 12739 RMVar_ID_12739 Human_SNP_ID_2875014 A-to-I Human chr1 - 10459916 10459916 10459916 TTAAATAAAGTAATTGTCAGCTTAGGCAACATAGCAAGACCCTGTCTCTACAAAAAAAAAATTTA TTAAATAAAGTAATTGTCAGCTTAGGCAACATGGCAAGACCCTGTCTCTACAAAAAAAAAATTTA T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1379631302 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9446419,Human_RBP_ID_23143030 12740 RMVar_ID_12740 Human_SNP_ID_2875016 A-to-I Human chr1 - 10459918 10459918 10459918 TTTTAAATAAAGTAATTGTCAGCTTAGGCAACATAGCAAGACCCTGTCTCTACAAAAAAAAAATT TTTTAAATAAAGTAATTGTCAGCTTAGGCAACGTAGCAAGACCCTGTCTCTACAAAAAAAAAATT T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1395034040 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9446419,Human_RBP_ID_23143030 12741 RMVar_ID_12741 Human_SNP_ID_2875019 A-to-I Human chr1 - 10459925 10459925 10459925 AAAAAGCTTTTAAATAAAGTAATTGTCAGCTTAGGCAACATAGCAAGACCCTGTCTCTACAAAAA AAAAAGCTTTTAAATAAAGTAATTGTCAGCTTGGGCAACATAGCAAGACCCTGTCTCTACAAAAA T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1327640723 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1721140,Human_RBP_ID_26576385 12742 RMVar_ID_12742 Human_SNP_ID_2875035 A-to-I Human chr1 - 10460000 10460000 10460000 CCTCAGGTGATCCACCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCACCCC CCTCAGGTGATCCACCCACCTCAGCCTCCCAAGGTGCTGGGATTACAGGTGTGAGCCACCACCCC T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1490696400 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3979306 12743 RMVar_ID_12743 Human_SNP_ID_2875038 A-to-I Human chr1 - 10460010 10460010 10460010 AAACTCCTGACCTCAGGTGATCCACCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG AAACTCCTGACCTCAGGTGATCCACCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE38233;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,30559470,31158229,31158229,31158229 RNA-Seq:(High) rs1175450704 Functional Loss SNV dbSNP153 33..33 33 - - - 12744 RMVar_ID_12744 Human_SNP_ID_2875045 A-to-I Human chr1 - 10460040 10460040 10460040 GGGTTTTGTCACATTGGCCAGGCTGGTCTCAAACTCCTGACCTCAGGTGATCCACCCACCTCAGC GGGTTTTGTCACATTGGCCAGGCTGGTCTCAAGCTCCTGACCTCAGGTGATCCACCCACCTCAGC T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1296224723 Functional Loss SNV dbSNP153 33..33 33 - - - 12745 RMVar_ID_12745 Human_SNP_ID_2875063 A-to-I Human chr1 - 10460097 10460097 10460097 GGGATTACAGGCACGTGCCACCATGCCCGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTTG GGGATTACAGGCACGTGCCACCATGCCCGGCTGATTTTTGTATTTTTAGTAGAGACAGGGTTTTG T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1365393156 Functional Loss SNV dbSNP153 33..33 33 - - - 12746 RMVar_ID_12746 Human_SNP_ID_2875075 A-to-I Human chr1 - 10460117 10460117 10460117 TTTCAGCCTCCTGAGCAGCTGGGATTACAGGCACGTGCCACCATGCCCGGCTAATTTTTGTATTT TTTCAGCCTCCTGAGCAGCTGGGATTACAGGCGCGTGCCACCATGCCCGGCTAATTTTTGTATTT T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1331672594 Functional Loss SNV dbSNP153 33..33 33 - - - 12747 RMVar_ID_12747 Human_SNP_ID_2875079 A-to-I Human chr1 - 10460133 10460133 10460133 TCAAGCGATTCTCCTGTTTCAGCCTCCTGAGCAGCTGGGATTACAGGCACGTGCCACCATGCCCG TCAAGCGATTCTCCTGTTTCAGCCTCCTGAGCGGCTGGGATTACAGGCACGTGCCACCATGCCCG T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1223842253 Functional Loss SNV dbSNP153 33..33 33 - - - 12748 RMVar_ID_12748 Human_SNP_ID_2875085 A-to-I Human chr1 - 10460145 10460145 10460145 CACCTCCCAGGTTCAAGCGATTCTCCTGTTTCAGCCTCCTGAGCAGCTGGGATTACAGGCACGTG CACCTCCCAGGTTCAAGCGATTCTCCTGTTTCGGCCTCCTGAGCAGCTGGGATTACAGGCACGTG T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1472809419 Functional Loss SNV dbSNP153 33..33 33 - - - 12749 RMVar_ID_12749 Human_SNP_ID_2875090 A-to-I Human chr1 - 10460162 10460162 10460162 CGGCTCACTGCAACCCCCACCTCCCAGGTTCAAGCGATTCTCCTGTTTCAGCCTCCTGAGCAGCT CGGCTCACTGCAACCCCCACCTCCCAGGTTCAGGCGATTCTCCTGTTTCAGCCTCCTGAGCAGCT T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1164855694 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27385197 12750 RMVar_ID_12750 Human_SNP_ID_2875091 A-to-I Human chr1 - 10460169 10460169 10460169 ACATTCTCGGCTCACTGCAACCCCCACCTCCCAGGTTCAAGCGATTCTCCTGTTTCAGCCTCCTG ACATTCTCGGCTCACTGCAACCCCCACCTCCCGGGTTCAAGCGATTCTCCTGTTTCAGCCTCCTG T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1348796652 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27385197 12751 RMVar_ID_12751 Human_SNP_ID_2875105 A-to-I Human chr1 - 10460201 10460201 10460201 TCACTCTGTCACCTAGTCTGGAGTGCAGTGGCACATTCTCGGCTCACTGCAACCCCCACCTCCCA TCACTCTGTCACCTAGTCTGGAGTGCAGTGGCGCATTCTCGGCTCACTGCAACCCCCACCTCCCA T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE100210;GSE112787 HepG2 cell line;293 Flip-In T-REx cells,empty vector - 29129909,29967493 RNA-Seq:(High) rs1290603364 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26364835 12752 RMVar_ID_12752 Human_SNP_ID_2875108 A-to-I Human chr1 - 10460207 10460207 10460207 AGAGTCTCACTCTGTCACCTAGTCTGGAGTGCAGTGGCACATTCTCGGCTCACTGCAACCCCCAC AGAGTCTCACTCTGTCACCTAGTCTGGAGTGCGGTGGCACATTCTCGGCTCACTGCAACCCCCAC T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs989020749 Functional Loss SNV dbSNP153 33..33 33 - - - 12753 RMVar_ID_12753 Human_SNP_ID_2875114 A-to-I Human chr1 - 10460231 10460229 10460231 AGTTTTGTTTTGTTTTTTTGAGACAGAGTCTCACTCTGTCACCTAGTCTGGAGTGCAGTGGCACA AGTTTTGTTTTGTTTTTTTGAGACAGAGTCTC__TCTGTCACCTAGTCTGGAGTGCAGTGGCACA AGT A DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs748227270 Functional Loss DEL dbSNP153 33..34 33 - - - 12754 RMVar_ID_12754 Human_SNP_ID_2875115 A-to-I Human chr1 - 10460231 10460231 10460231 AGTTTTGTTTTGTTTTTTTGAGACAGAGTCTCACTCTGTCACCTAGTCTGGAGTGCAGTGGCACA AGTTTTGTTTTGTTTTTTTGAGACAGAGTCTCGCTCTGTCACCTAGTCTGGAGTGCAGTGGCACA T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1403124520 Functional Loss SNV dbSNP153 33..33 33 - - - 12755 RMVar_ID_12755 Human_SNP_ID_2875121 A-to-I Human chr1 - 10460239 10460238 10460240 AAAAAAAAAGTTTTGTTTTGTTTTTTTGAGACAGAGTCTCACTCTGTCACCTAGTCTGGAGTGCA AAAAAAAAAGTTTTGTTTTGTTTTTTTGAGA__GAGTCTCACTCTGTCACCTAGTCTGGAGTGCA CTG C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1450399030 Functional Loss DEL dbSNP153 32..33 33 - - - 12756 RMVar_ID_12756 Human_SNP_ID_2875143 A-to-I Human chr1 - 10460296 10460296 10460296 AGAGCGCACCACTGCACTCCAGCCTGGGTGACAGAGCTAGACTCCGTATCTCAAGAAAAAAAAAA AGAGCGCACCACTGCACTCCAGCCTGGGTGACGGAGCTAGACTCCGTATCTCAAGAAAAAAAAAA T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs942079673 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22369373,Human_RBP_ID_26385197 12757 RMVar_ID_12757 Human_SNP_ID_2875151 A-to-I Human chr1 - 10460321 10460321 10460321 GGTAGGCAGAGGTTGCAGTGAGCTGAGAGCGCACCACTGCACTCCAGCCTGGGTGACAGAGCTAG GGTAGGCAGAGGTTGCAGTGAGCTGAGAGCGCGCCACTGCACTCCAGCCTGGGTGACAGAGCTAG T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1295352069 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9553653,Human_RBP_ID_17556521,Human_RBP_ID_22369373,Human_RBP_ID_26364836 12758 RMVar_ID_12758 Human_SNP_ID_2875155 A-to-I Human chr1 - 10460326 10460326 10460326 TACTCGGTAGGCAGAGGTTGCAGTGAGCTGAGAGCGCACCACTGCACTCCAGCCTGGGTGACAGA TACTCGGTAGGCAGAGGTTGCAGTGAGCTGAGGGCGCACCACTGCACTCCAGCCTGGGTGACAGA T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1440338070 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17556521,Human_RBP_ID_22369373,Human_RBP_ID_26385198 12759 RMVar_ID_12759 Human_SNP_ID_2875177 A-to-I Human chr1 - 10460382 10460382 10460382 TCTACTAAAAATACAAAAATTAGCTGGGCATGATGGCGGGTGCCTGTAATCCCAGCTACTCGGTA TCTACTAAAAATACAAAAATTAGCTGGGCATGGTGGCGGGTGCCTGTAATCCCAGCTACTCGGTA T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE38233;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;ASD brains,Fragile X samples from NIH NeuroBioBank;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,30559470,31158229,31158229 RNA-Seq:(High) rs570816974 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17556521 12760 RMVar_ID_12760 Human_SNP_ID_2875183 A-to-I Human chr1 - 10460393 10460393 10460393 GAAACCCCGTCTCTACTAAAAATACAAAAATTAGCTGGGCATGATGGCGGGTGCCTGTAATCCCA GAAACCCCGTCTCTACTAAAAATACAAAAATTGGCTGGGCATGATGGCGGGTGCCTGTAATCCCA T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1268406615 Functional Loss SNV dbSNP153 33..33 33 - - - 12761 RMVar_ID_12761 Human_SNP_ID_2875196 A-to-I Human chr1 - 10460430 10460430 10460430 GAGGTCAGGAGTTCAAGACCAACCTGGCCAATATGGTGAAACCCCGTCTCTACTAAAAATACAAA GAGGTCAGGAGTTCAAGACCAACCTGGCCAATGTGGTGAAACCCCGTCTCTACTAAAAATACAAA T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1392980569 Functional Loss SNV dbSNP153 33..33 33 - - - 12762 RMVar_ID_12762 Human_SNP_ID_2875205 A-to-I Human chr1 - 10460456 10460456 10460456 TGGAGGCCGATGCAGGCGGATCACATGAGGTCAGGAGTTCAAGACCAACCTGGCCAATATGGTGA TGGAGGCCGATGCAGGCGGATCACATGAGGTCGGGAGTTCAAGACCAACCTGGCCAATATGGTGA T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1236435130 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10500282 12763 RMVar_ID_12763 Human_SNP_ID_2875213 A-to-I Human chr1 - 10460475 10460475 10460475 ACCTTTGATCCCAGCACTTTGGAGGCCGATGCAGGCGGATCACATGAGGTCAGGAGTTCAAGACC ACCTTTGATCCCAGCACTTTGGAGGCCGATGCGGGCGGATCACATGAGGTCAGGAGTTCAAGACC T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1184762761 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10500282,Human_RBP_ID_26364837 12764 RMVar_ID_12764 Human_SNP_ID_2875297 A-to-I Human chr1 - 10460678 10460678 10460678 AAAAGTACAAAAAACTAGCTGGGCGTGGTGGCAGGAGCCTGTAGTCCCAGCTACTCGGGAGGCTG AAAAGTACAAAAAACTAGCTGGGCGTGGTGGCGGGAGCCTGTAGTCCCAGCTACTCGGGAGGCTG T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1041525111 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5664043,Human_RBP_ID_26385201 12765 RMVar_ID_12765 Human_SNP_ID_2875303 A-to-I Human chr1 - 10460694 10460694 10460694 GAAACGTGTTTTTACTAAAAGTACAAAAAACTAGCTGGGCGTGGTGGCAGGAGCCTGTAGTCCCA GAAACGTGTTTTTACTAAAAGTACAAAAAACTGGCTGGGCGTGGTGGCAGGAGCCTGTAGTCCCA T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1413686371 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5664043,Human_RBP_ID_26385201 12766 RMVar_ID_12766 Human_SNP_ID_2875305 A-to-I Human chr1 - 10460707 10460707 10460707 TGGCTAACACAGTGAAACGTGTTTTTACTAAAAGTACAAAAAACTAGCTGGGCGTGGTGGCAGGA TGGCTAACACAGTGAAACGTGTTTTTACTAAAGGTACAAAAAACTAGCTGGGCGTGGTGGCAGGA T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1157766659 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8953234,Human_RBP_ID_18213999 12767 RMVar_ID_12767 Human_SNP_ID_2875327 A-to-I Human chr1 - 10460762 10460762 10460762 GCACTTTGGGAGGCCGAGGCGGGTGGATCACGAGGTCAGGAGATCGAGACCATCCTGGCTAACAC GCACTTTGGGAGGCCGAGGCGGGTGGATCACGGGGTCAGGAGATCGAGACCATCCTGGCTAACAC T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs1425007693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26385202 12768 RMVar_ID_12768 Human_SNP_ID_2875437 A-to-I Human chr1 - 10461047 10461047 10461047 AAAATTAGCCAGCCATGGTGGCGGGCGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGA AAAATTAGCCAGCCATGGTGGCGGGCGCCTGTGATCCCAGCTACTTGGGAGGCTGAGGCAGGAGA T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1363505455 Functional Loss SNV dbSNP153 33..33 33 - - - 12769 RMVar_ID_12769 Human_SNP_ID_2875451 A-to-I Human chr1 - 10461069 10461069 10461069 TGTCTCTACTAAAAATACAAAAAAAATTAGCCAGCCATGGTGGCGGGCGCCTGTAATCCCAGCTA TGTCTCTACTAAAAATACAAAAAAAATTAGCCGGCCATGGTGGCGGGCGCCTGTAATCCCAGCTA T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE38233;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;ASD brains,Fragile X samples from NIH NeuroBioBank;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,30559470,31158229,31158229 RNA-Seq:(High) rs1179747889 Functional Loss SNV dbSNP153 33..33 33 - - - 12770 RMVar_ID_12770 Human_SNP_ID_2875453 A-to-I Human chr1 - 10461073 10461073 10461073 ACCCTGTCTCTACTAAAAATACAAAAAAAATTAGCCAGCCATGGTGGCGGGCGCCTGTAATCCCA ACCCTGTCTCTACTAAAAATACAAAAAAAATTGGCCAGCCATGGTGGCGGGCGCCTGTAATCCCA T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831 HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line - 29129909,32596459 RNA-Seq:(High) rs1370278078 Functional Loss SNV dbSNP153 33..33 33 - - - 12771 RMVar_ID_12771 Human_SNP_ID_2875476 A-to-I Human chr1 - 10461105 10461105 10461105 GAGATCGAGACCATCCTGGCTAACATGGTGAAACCCTGTCTCTACTAAAAATACAAAAAAAATTA GAGATCGAGACCATCCTGGCTAACATGGTGAAGCCCTGTCTCTACTAAAAATACAAAAAAAATTA T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE47997;GSE38233;GSE99789 K562 cells&HepG2 cells;cultured B-cells;esophageal squamous carcinoma cells,EC109 - 23474544,24183664,29796672 RNA-Seq:(High) rs1194311937 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_101955 12772 RMVar_ID_12772 Human_SNP_ID_2875482 A-to-I Human chr1 - 10461113 10461113 10461113 GAAGTCAGGAGATCGAGACCATCCTGGCTAACATGGTGAAACCCTGTCTCTACTAAAAATACAAA GAAGTCAGGAGATCGAGACCATCCTGGCTAACGTGGTGAAACCCTGTCTCTACTAAAAATACAAA T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs1241175453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_101955 12773 RMVar_ID_12773 Human_SNP_ID_2875485 A-to-I Human chr1 - 10461115 10461115 10461115 GTGAAGTCAGGAGATCGAGACCATCCTGGCTAACATGGTGAAACCCTGTCTCTACTAAAAATACA GTGAAGTCAGGAGATCGAGACCATCCTGGCTAGCATGGTGAAACCCTGTCTCTACTAAAAATACA T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1263133108 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_101955 12774 RMVar_ID_12774 Human_SNP_ID_2875508 A-to-I Human chr1 - 10461143 10461143 10461143 AGCACTGGGAGGCCGAGGGGGGCGGATCGTGAAGTCAGGAGATCGAGACCATCCTGGCTAACATG AGCACTGGGAGGCCGAGGGGGGCGGATCGTGAGGTCAGGAGATCGAGACCATCCTGGCTAACATG T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1135131 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_101956,Human_RBP_ID_5664045,Human_RBP_ID_26364841 Human_miRNA_ID_1005266 12775 RMVar_ID_12775 Human_SNP_ID_2875535 A-to-I Human chr1 - 10461180 10461180 10461180 TGATTGGCCAGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTGGGAGGCCGAGGGGGGCGGATC TGATTGGCCAGGCGCAGTGGCTCACGCCTGTAGTCCCAGCACTGGGAGGCCGAGGGGGGCGGATC T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1409482300 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224336,Human_RBP_ID_8167620,Human_RBP_ID_26387328 12776 RMVar_ID_12776 Human_SNP_ID_2875536 A-to-I Human chr1 - 10461181 10461181 10461181 GTGATTGGCCAGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTGGGAGGCCGAGGGGGGCGGAT GTGATTGGCCAGGCGCAGTGGCTCACGCCTGTGATCCCAGCACTGGGAGGCCGAGGGGGGCGGAT T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,29796672,31158229 RNA-Seq:(High) rs1419125687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224336,Human_RBP_ID_8167620,Human_RBP_ID_26387328 12777 RMVar_ID_12777 Human_SNP_ID_2875548 A-to-I Human chr1 - 10461197 10461197 10461197 TCAAAAGTAATTGGCAGTGATTGGCCAGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTGGGAG TCAAAAGTAATTGGCAGTGATTGGCCAGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTGGGAG T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1057026 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_319427,Human_RBP_ID_8167620,Human_RBP_ID_10500289,Human_RBP_ID_26387328 12778 RMVar_ID_12778 Human_SNP_ID_2875552 A-to-I Human chr1 - 10461203 10461203 10461203 CTCTGTTCAAAAGTAATTGGCAGTGATTGGCCAGGCGCAGTGGCTCACGCCTGTAATCCCAGCAC CTCTGTTCAAAAGTAATTGGCAGTGATTGGCCGGGCGCAGTGGCTCACGCCTGTAATCCCAGCAC T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs767375414 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_319427,Human_RBP_ID_8167620,Human_RBP_ID_10500289,Human_RBP_ID_17719867,Human_RBP_ID_26387328 Human_miRNA_ID_876957,Human_miRNA_ID_1346431,Human_miRNA_ID_1808264 12779 RMVar_ID_12779 Human_SNP_ID_2875803 A-to-I Human chr1 - 10461918 10461918 10461918 TCCGGGAGGCGGAGCTTGCAGGGAGCCGAGATAGTGTCACTGCACTCCAGCCTGGGTGACAGAGC TCCGGGAGGCGGAGCTTGCAGGGAGCCGAGATCGTGTCACTGCACTCCAGCCTGGGTGACAGAGC T G DFFA Ensembl:ENSG00000160049 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1455811565 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_319440,Human_RBP_ID_24568007 12780 RMVar_ID_12780 Human_SNP_ID_2876021 A-to-I Human chr1 - 10462248 10462248 10462248 GGGAGGCTGAAGCAAGAGAATCACTTGAACCCAGGAGGTGGAGGTTGCGTGAGCTAAGATCGCGC GGGAGGCTGAAGCAAGAGAATCACTTGAACCCGGGAGGTGGAGGTTGCGTGAGCTAAGATCGCGC T C DFFA Ensembl:ENSG00000160049 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1295336052 Functional Loss SNV dbSNP153 33..33 33 - - - 12781 RMVar_ID_12781 Human_SNP_ID_2876702 A-to-I Human chr1 - 10464663 10464663 10464663 TCACCCAGGCTGGAGTGCAGTAGTGCAATCTCAGCTCACTGCACCATCTGCCTGCTGGGCTCAAG TCACCCAGGCTGGAGTGCAGTAGTGCAATCTCTGCTCACTGCACCATCTGCCTGCTGGGCTCAAG T A DFFA Ensembl:ENSG00000160049 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1304439904 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102222,RMVar_hsa_circ_322189,RMVar_hsa_circ_129016,RMVar_hsa_circ_129017 12782 RMVar_ID_12782 Human_SNP_ID_2887005 A-to-I Human chr1 + 10505064 10505064 10505064 CACCTTGGCCTCCCTCCCAAAGTGTTGGAATTACAGGCATGAGCCACCATACCTGGCCAATGATT CACCTTGGCCTCCCTCCCAAAGTGTTGGAATTGCAGGCATGAGCCACCATACCTGGCCAATGATT A G PEX14 Ensembl:ENSG00000142655 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1205712816 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92275,RMVar_hsa_circ_129020 12783 RMVar_ID_12783 Human_SNP_ID_2895946 A-to-I Human chr1 + 10543336 10543336 10543336 TTTGTAGTTTTTGGTAGAGATGGGGTTTTACCATCTTGGCCAGGCTGGTCTTGAACTCCTGATCT TTTGTAGTTTTTGGTAGAGATGGGGTTTTACCGTCTTGGCCAGGCTGGTCTTGAACTCCTGATCT A G PEX14 Ensembl:ENSG00000142655 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs955883377 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92275,RMVar_hsa_circ_32108,RMVar_hsa_circ_129020,RMVar_hsa_circ_89373,RMVar_hsa_circ_300186,RMVar_hsa_circ_129022,RMVar_hsa_circ_129023 12784 RMVar_ID_12784 Human_SNP_ID_2895954 A-to-I Human chr1 + 10543370 10543370 10543370 CTTGGCCAGGCTGGTCTTGAACTCCTGATCTCATGATTCACCTGTCTCGGCCTCTCAAAGTGCTG CTTGGCCAGGCTGGTCTTGAACTCCTGATCTCGTGATTCACCTGTCTCGGCCTCTCAAAGTGCTG A G PEX14 Ensembl:ENSG00000142655 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1196664535 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92275,RMVar_hsa_circ_32108,RMVar_hsa_circ_129020,RMVar_hsa_circ_89373,RMVar_hsa_circ_300186,RMVar_hsa_circ_129022,RMVar_hsa_circ_129023 12785 RMVar_ID_12785 Human_SNP_ID_2896025 A-to-I Human chr1 + 10543662 10543662 10543662 ATTATATAACAGTATTGCCTAGGCTGGAATGTAATGGCATGATCATAGCTCACTGAAGCCTTGAA ATTATATAACAGTATTGCCTAGGCTGGAATGTGATGGCATGATCATAGCTCACTGAAGCCTTGAA A G PEX14 Ensembl:ENSG00000142655 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054269045 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92275,RMVar_hsa_circ_32108,RMVar_hsa_circ_129020,RMVar_hsa_circ_89373,RMVar_hsa_circ_300186,RMVar_hsa_circ_129022,RMVar_hsa_circ_129023 12786 RMVar_ID_12786 Human_SNP_ID_2896058 A-to-I Human chr1 + 10543789 10543789 10543789 CCACCACACCTGGTGAGTTTTTTTGTAGAGACAGGGTCTCACTGTGTTTCCCAGGCTGGTCTCAA CCACCACACCTGGTGAGTTTTTTTGTAGAGACGGGGTCTCACTGTGTTTCCCAGGCTGGTCTCAA A G PEX14 Ensembl:ENSG00000142655 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1346922133 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92275,RMVar_hsa_circ_32108,RMVar_hsa_circ_129020,RMVar_hsa_circ_89373,RMVar_hsa_circ_300186,RMVar_hsa_circ_129022,RMVar_hsa_circ_129023 12787 RMVar_ID_12787 Human_SNP_ID_2896078 A-to-I Human chr1 + 10543865 10543865 10543865 CAAGTCATCCTTCTGCCTTGCCTTCCCAAAGCATTGGAATTACAGACATGAACCACGGCACCTGG CAAGTCATCCTTCTGCCTTGCCTTCCCAAAGCGTTGGAATTACAGACATGAACCACGGCACCTGG A G PEX14 Ensembl:ENSG00000142655 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs932575458 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10501011 RMVar_hsa_circ_92275,RMVar_hsa_circ_32108,RMVar_hsa_circ_129020,RMVar_hsa_circ_89373,RMVar_hsa_circ_300186,RMVar_hsa_circ_129022,RMVar_hsa_circ_129023 12788 RMVar_ID_12788 Human_SNP_ID_2896080 A-to-I Human chr1 + 10543880 10543880 10543880 CCTTGCCTTCCCAAAGCATTGGAATTACAGACATGAACCACGGCACCTGGCCCATGGAGCACAGA CCTTGCCTTCCCAAAGCATTGGAATTACAGACGTGAACCACGGCACCTGGCCCATGGAGCACAGA A G PEX14 Ensembl:ENSG00000142655 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs890755360 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10501011 RMVar_hsa_circ_92275,RMVar_hsa_circ_32108,RMVar_hsa_circ_129020,RMVar_hsa_circ_89373,RMVar_hsa_circ_300186,RMVar_hsa_circ_129022,RMVar_hsa_circ_129023 12789 RMVar_ID_12789 Human_SNP_ID_2896309 A-to-I Human chr1 + 10544862 10544862 10544862 CGGTTCACTGCAGCCTTGACCTCCCCGGGATCAAGTGATCCTCCCATCGCAGCCTCCCAGGTAGC CGGTTCACTGCAGCCTTGACCTCCCCGGGATCGAGTGATCCTCCCATCGCAGCCTCCCAGGTAGC A G PEX14 Ensembl:ENSG00000142655 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs970450156 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92275,RMVar_hsa_circ_32108,RMVar_hsa_circ_129020,RMVar_hsa_circ_89373,RMVar_hsa_circ_300186,RMVar_hsa_circ_129022,RMVar_hsa_circ_129023 12790 RMVar_ID_12790 Human_SNP_ID_2896543 A-to-I Human chr1 + 10545947 10545947 10545947 CATGCCTGTGGTTCCAGCTACTTGAGAGGCTGAGGCAGGAGGATTGCTTGAGCCTTGGAGTTTGA CATGCCTGTGGTTCCAGCTACTTGAGAGGCTGGGGCAGGAGGATTGCTTGAGCCTTGGAGTTTGA A G PEX14 Ensembl:ENSG00000142655 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs887893443 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92275,RMVar_hsa_circ_32108,RMVar_hsa_circ_129020,RMVar_hsa_circ_89373,RMVar_hsa_circ_300186,RMVar_hsa_circ_129022,RMVar_hsa_circ_129023 12791 RMVar_ID_12791 Human_SNP_ID_2896544 A-to-I Human chr1 + 10545947 10545947 10545947 CATGCCTGTGGTTCCAGCTACTTGAGAGGCTGAGGCAGGAGGATTGCTTGAGCCTTGGAGTTTGA CATGCCTGTGGTTCCAGCTACTTGAGAGGCTGTGGCAGGAGGATTGCTTGAGCCTTGGAGTTTGA A T PEX14 Ensembl:ENSG00000142655 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs887893443 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92275,RMVar_hsa_circ_32108,RMVar_hsa_circ_129020,RMVar_hsa_circ_89373,RMVar_hsa_circ_300186,RMVar_hsa_circ_129022,RMVar_hsa_circ_129023 12792 RMVar_ID_12792 Human_SNP_ID_2896653 A-to-I Human chr1 + 10546444 10546443 10546444 AAAATTAGCCGGGTGTGGTGACGCTTACCTGTAAACCAAGCTACTTTGGAGGCTGAGGCAGGAGA AAAATTAGCCGGGTGTGGTGACGCTTACCTGT_AACCAAGCTACTTTGGAGGCTGAGGCAGGAGA TA T PEX14 Ensembl:ENSG00000142655 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1316151558 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_92275,RMVar_hsa_circ_32108,RMVar_hsa_circ_129020,RMVar_hsa_circ_89373,RMVar_hsa_circ_300186,RMVar_hsa_circ_129022,RMVar_hsa_circ_129023 12793 RMVar_ID_12793 Human_SNP_ID_2903937 A-to-I Human chr1 + 10576826 10576826 10576826 ATCGCCCAAGCTGGAGTGCGTGGCGCGATCTCAGCACACTGCAACCTCTGCTTCCCAGGTTCAAG ATCGCCCAAGCTGGAGTGCGTGGCGCGATCTCGGCACACTGCAACCTCTGCTTCCCAGGTTCAAG A G PEX14 Ensembl:ENSG00000142655 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1020723009 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92275,RMVar_hsa_circ_32108,RMVar_hsa_circ_129020,RMVar_hsa_circ_89373,RMVar_hsa_circ_300186,RMVar_hsa_circ_129022,RMVar_hsa_circ_129023 12794 RMVar_ID_12794 Human_SNP_ID_2903989 A-to-I Human chr1 + 10577032 10577032 10577032 CTAAAGCTCTAGGATTACAGGCGTGAGCCACCACACCCAGCCTAATTGCTGTATCTTTATTATCA CTAAAGCTCTAGGATTACAGGCGTGAGCCACCTCACCCAGCCTAATTGCTGTATCTTTATTATCA A T PEX14 Ensembl:ENSG00000142655 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs938864632 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92275,RMVar_hsa_circ_32108,RMVar_hsa_circ_129020,RMVar_hsa_circ_89373,RMVar_hsa_circ_300186,RMVar_hsa_circ_129022,RMVar_hsa_circ_129023 12795 RMVar_ID_12795 Human_SNP_ID_2905159 A-to-I Human chr1 + 10581406 10581399 10581407 TCGGCTCACTGCAACCTGTGTCTCCTGGTTTCAAGCAATTCTCTGTCTCAGCCTCCCGAGTAGTT TCGGCTCACTGCAACCTGTGTCTCCT________GCAATTCTCTGTCTCAGCCTCCCGAGTAGTT TGGTTTCAA T PEX14 Ensembl:ENSG00000142655 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1450378021 Functional Loss DEL dbSNP153 27..34 33 - - - RMVar_hsa_circ_32108,RMVar_hsa_circ_89373,RMVar_hsa_circ_300186,RMVar_hsa_circ_129022,RMVar_hsa_circ_129023 12796 RMVar_ID_12796 Human_SNP_ID_2911300 A-to-I Human chr1 + 10607999 10607999 10607999 CTCCTATATTGTCTTCTAGGAGACACTGTCTCACTCTGTCACCCAGGCTGGAATGCAATGGCCTG CTCCTATATTGTCTTCTAGGAGACACTGTCTCTCTCTGTCACCCAGGCTGGAATGCAATGGCCTG A T PEX14 Ensembl:ENSG00000142655 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1446011259 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8279671 RMVar_hsa_circ_32108,RMVar_hsa_circ_89373,RMVar_hsa_circ_129023 12797 RMVar_ID_12797 Human_SNP_ID_3022789 A-to-I Human chr1 + 11016377 11016377 11016377 TAGGCACACTGCAGCCTCAAACTCCTGGACTCAAGTCGTCCTTCCTCCTCAGCCTCCTGAGTTGC TAGGCACACTGCAGCCTCAAACTCCTGGACTCGAGTCGTCCTTCCTCCTCAGCCTCCTGAGTTGC A G AL109811.3,TARDBP Ensembl:ENSG00000277726,Ensembl:ENSG00000120948 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1347363107 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54309,RMVar_hsa_circ_378714,RMVar_hsa_circ_347891,RMVar_hsa_circ_14990 12798 RMVar_ID_12798 Human_SNP_ID_3024025 A-to-I Human chr1 + 11020653 11020653 11020653 TGTCCCGGCCGGGCGTGGTGGCTCATGCTTACAATCCCAGCACTTTGGAGGCCGAGGCGGGTGGA TGTCCCGGCCGGGCGTGGTGGCTCATGCTTACCATCCCAGCACTTTGGAGGCCGAGGCGGGTGGA A C AL109811.3,TARDBP Ensembl:ENSG00000277726,Ensembl:ENSG00000120948 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs931088236 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54309,RMVar_hsa_circ_347891,RMVar_hsa_circ_51795,RMVar_hsa_circ_12595 12799 RMVar_ID_12799 Human_SNP_ID_3024093 A-to-I Human chr1 + 11020869 11020869 11020869 CCAGGAGGCGGAGGTGGCAGTGAACTGAGATCACACCACTGCATTCCAGCCCAGTGACAGAGTGA CCAGGAGGCGGAGGTGGCAGTGAACTGAGATCCCACCACTGCATTCCAGCCCAGTGACAGAGTGA A C AL109811.3,TARDBP Ensembl:ENSG00000277726,Ensembl:ENSG00000120948 Protein coding,Protein coding intron,intron GSE38233;GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,32596459 RNA-Seq:(High) rs1379431449 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22844216,Human_RBP_ID_24570326 RMVar_hsa_circ_54309,RMVar_hsa_circ_347891,RMVar_hsa_circ_51795,RMVar_hsa_circ_12595 12800 RMVar_ID_12800 Human_SNP_ID_3024223 A-to-I Human chr1 + 11021268 11021268 11021268 TCAAGCGATTGTCTTGGCTCAGCCTCCTGAGTAGCTGGGATTACAGGTGCCTGCCACCACGCCTG TCAAGCGATTGTCTTGGCTCAGCCTCCTGAGTCGCTGGGATTACAGGTGCCTGCCACCACGCCTG A C AL109811.3,TARDBP Ensembl:ENSG00000277726,Ensembl:ENSG00000120948 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1162790306 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10512667 RMVar_hsa_circ_54309,RMVar_hsa_circ_347891,RMVar_hsa_circ_51795,RMVar_hsa_circ_12595 12801 RMVar_ID_12801 Human_SNP_ID_3024395 A-to-I Human chr1 + 11021864 11021864 11021864 GTCTTGAACTATTGGCCTCACACAGTCCTCCCACCTTGGCCTCCCAAAGCGCTAGGATTACAGGC GTCTTGAACTATTGGCCTCACACAGTCCTCCCCCCTTGGCCTCCCAAAGCGCTAGGATTACAGGC A C AL109811.3,TARDBP Ensembl:ENSG00000277726,Ensembl:ENSG00000120948 Protein coding,Protein coding intron,intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs575542474 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8280500,Human_RBP_ID_10512708,Human_RBP_ID_17556954 RMVar_hsa_circ_54309,RMVar_hsa_circ_347891,RMVar_hsa_circ_51795,RMVar_hsa_circ_12595 12802 RMVar_ID_12802 Human_SNP_ID_3024396 A-to-I Human chr1 + 11021864 11021864 11021864 GTCTTGAACTATTGGCCTCACACAGTCCTCCCACCTTGGCCTCCCAAAGCGCTAGGATTACAGGC GTCTTGAACTATTGGCCTCACACAGTCCTCCCGCCTTGGCCTCCCAAAGCGCTAGGATTACAGGC A G AL109811.3,TARDBP Ensembl:ENSG00000277726,Ensembl:ENSG00000120948 Protein coding,Protein coding intron,intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs575542474 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8280500,Human_RBP_ID_10512708,Human_RBP_ID_17556954 RMVar_hsa_circ_54309,RMVar_hsa_circ_347891,RMVar_hsa_circ_51795,RMVar_hsa_circ_12595 12803 RMVar_ID_12803 Human_SNP_ID_3024404 A-to-I Human chr1 + 11021885 11021885 11021885 ACAGTCCTCCCACCTTGGCCTCCCAAAGCGCTAGGATTACAGGCATGAGCCACCATGCCCAGCCT ACAGTCCTCCCACCTTGGCCTCCCAAAGCGCTGGGATTACAGGCATGAGCCACCATGCCCAGCCT A G AL109811.3,TARDBP Ensembl:ENSG00000277726,Ensembl:ENSG00000120948 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1138362 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18547054 RMVar_hsa_circ_54309,RMVar_hsa_circ_347891,RMVar_hsa_circ_51795,RMVar_hsa_circ_12595 12804 RMVar_ID_12804 Human_SNP_ID_3026128 A-to-I Human chr1 + 11027960 11027960 11027960 AGATTGGGAAAATTGGCCGGGTGCAGTGTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGAT AGATTGGGAAAATTGGCCGGGTGCAGTGTCACCCCTGTAATCCCAGCACTTTGGGAGGCTGAGAT A C AL109811.3 Ensembl:ENSG00000277726 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1262539545 Functional Loss SNV dbSNP153 33..33 33 - - - 12805 RMVar_ID_12805 Human_SNP_ID_3026176 A-to-I Human chr1 + 11028166 11028166 11028166 GTTGCTTGAACCTGGGAGGCGGAGGTTGCAGTAAGACAAGTCACACCACTGCACTCTAGCCTGGT GTTGCTTGAACCTGGGAGGCGGAGGTTGCAGTGAGACAAGTCACACCACTGCACTCTAGCCTGGT A G AL109811.3 Ensembl:ENSG00000277726 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1020914063 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24749997 12806 RMVar_ID_12806 Human_SNP_ID_3026184 A-to-I Human chr1 - 11028190 11028190 11028190 TTTTTGAGATGGAGTTTTGCTCTTACCAGGCTAGAGTGCAGTGGTGTGACTTGTCTTACTGCAAC TTTTTGAGATGGAGTTTTGCTCTTACCAGGCTGGAGTGCAGTGGTGTGACTTGTCTTACTGCAAC T C MASP2 Ensembl:ENSG00000009724 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1477899275 Functional Loss SNV dbSNP153 33..33 33 - - - 12807 RMVar_ID_12807 Human_SNP_ID_3026736 A-to-I Human chr1 + 11029728 11029728 11029728 TAATGGTGCGATCTGGGCTCACCGCAACCTCCACCACCTGGGTTCAAGCAATTCTGCCTCAGCCG TAATGGTGCGATCTGGGCTCACCGCAACCTCCTCCACCTGGGTTCAAGCAATTCTGCCTCAGCCG A T AL109811.3,AL109811.2 Ensembl:ENSG00000277726,Ensembl:ENSG00000271895 Protein coding,lincRNA intron,exon GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1020843428 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_16776 12808 RMVar_ID_12808 Human_SNP_ID_3026739 A-to-I Human chr1 + 11029741 11029741 11029741 TGGGCTCACCGCAACCTCCACCACCTGGGTTCAAGCAATTCTGCCTCAGCCGCTCGAGTAGCTGG TGGGCTCACCGCAACCTCCACCACCTGGGTTCGAGCAATTCTGCCTCAGCCGCTCGAGTAGCTGG A G AL109811.3,AL109811.2 Ensembl:ENSG00000277726,Ensembl:ENSG00000271895 Protein coding,lincRNA intron,exon GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 29129909,30559470 RNA-Seq:(High) rs1322204259 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_16776 12809 RMVar_ID_12809 Human_SNP_ID_3026760 A-to-I Human chr1 + 11029821 11029821 11029821 CCACCACACCCGGCTAATTTTGTATTTTTATTAGAGACGGGGTTTCTCCATGCTGGTCAGGCTGG CCACCACACCCGGCTAATTTTGTATTTTTATTGGAGACGGGGTTTCTCCATGCTGGTCAGGCTGG A G AL109811.3,AL109811.2 Ensembl:ENSG00000277726,Ensembl:ENSG00000271895 Protein coding,lincRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1427543450 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10513948 12810 RMVar_ID_12810 Human_SNP_ID_3035885 A-to-I Human chr1 - 11057881 11057879 11057881 CCAGCTACTAGGGAGGCTGAGGTGGAAGAATTACTTGAGCCCGGGAGGCGGAAGTTGCAATGAAC CCAGCTACTAGGGAGGCTGAGGTGGAAGAATT__TTGAGCCCGGGAGGCGGAAGTTGCAATGAAC AGT A SRM Ensembl:ENSG00000116649 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1397769977 Functional Loss DEL dbSNP153 33..34 33 - - - 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_129039,RMVar_hsa_circ_125542 12811 RMVar_ID_12811 Human_SNP_ID_3036015 A-to-I Human chr1 - 11058390 11058390 11058390 TGCCCGGCTAATTTTGTATTTTTAGTAGAGACAGGGTTTCTCCATGTTGGTCAGGCTGGTCTCGG TGCCCGGCTAATTTTGTATTTTTAGTAGAGACGGGGTTTCTCCATGTTGGTCAGGCTGGTCTCGG T C SRM Ensembl:ENSG00000116649 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1220672646 Functional Loss SNV dbSNP153 33..33 33 - - - 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_129039,RMVar_hsa_circ_125542 12812 RMVar_ID_12812 Human_SNP_ID_3036033 A-to-I Human chr1 - 11058475 11058475 11058475 CTCACTGCAACCTCCACCTCCTGGGCTCAAGTAGTTCTTCTGCCTCAGCCTCCGGAGTAGCTGGG CTCACTGCAACCTCCACCTCCTGGGCTCAAGTGGTTCTTCTGCCTCAGCCTCCGGAGTAGCTGGG T C SRM Ensembl:ENSG00000116649 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs367927509 Functional Loss SNV dbSNP153 33..33 33 - - - 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_129039,RMVar_hsa_circ_125542 12813 RMVar_ID_12813 Human_SNP_ID_3040310 A-to-I Human chr1 - 11073179 11073179 11073179 GCAGTGAGCCGAGGTTGCGCCACTGCGCTCCAACCTGCGCGACAGAGCGAACTCTAGCCAAAAAA GCAGTGAGCCGAGGTTGCGCCACTGCGCTCCATCCTGCGCGACAGAGCGAACTCTAGCCAAAAAA T A EXOSC10 Ensembl:ENSG00000171824 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1020583911 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19042661 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_8396,RMVar_hsa_circ_129041,RMVar_hsa_circ_129042,RMVar_hsa_circ_129043,RMVar_hsa_circ_106658,RMVar_hsa_circ_129044 12814 RMVar_ID_12814 Human_SNP_ID_3040311 A-to-I Human chr1 - 11073179 11073179 11073179 GCAGTGAGCCGAGGTTGCGCCACTGCGCTCCAACCTGCGCGACAGAGCGAACTCTAGCCAAAAAA GCAGTGAGCCGAGGTTGCGCCACTGCGCTCCAGCCTGCGCGACAGAGCGAACTCTAGCCAAAAAA T C EXOSC10 Ensembl:ENSG00000171824 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1020583911 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19042661 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_8396,RMVar_hsa_circ_129041,RMVar_hsa_circ_129042,RMVar_hsa_circ_129043,RMVar_hsa_circ_106658,RMVar_hsa_circ_129044 12815 RMVar_ID_12815 Human_SNP_ID_3040902 A-to-I Human chr1 - 11075093 11075093 11075093 AGGAGGCGGAGGTTGCAGTGAGCAGAGATGGCACCACTGCACTCCAACCTGGGCAACAGAGCAAG AGGAGGCGGAGGTTGCAGTGAGCAGAGATGGCGCCACTGCACTCCAACCTGGGCAACAGAGCAAG T C EXOSC10 Ensembl:ENSG00000171824 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1161522850 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10516667,Human_RBP_ID_24571332 RMVar_hsa_circ_98158,RMVar_hsa_circ_4265,RMVar_hsa_circ_289591,RMVar_hsa_circ_278266,RMVar_hsa_circ_367755,RMVar_hsa_circ_83091,RMVar_hsa_circ_8396,RMVar_hsa_circ_129042,RMVar_hsa_circ_129043,RMVar_hsa_circ_106658,RMVar_hsa_circ_127325,RMVar_hsa_circ_129044,RMVar_hsa_circ_279195,RMVar_hsa_circ_321722,RMVar_hsa_circ_121445,RMVar_hsa_circ_129047,RMVar_hsa_circ_129049,RMVar_hsa_circ_129048,RMVar_hsa_circ_129046 12816 RMVar_ID_12816 Human_SNP_ID_3041738 A-to-I Human chr1 - 11078127 11078125 11078127 GGGACCACAGGCATACACCACCATACCCAGCTATGTTTTTTTTAATTTTTTGTAGAGATGGGTCT GGGACCACAGGCATACACCACCATACCCAGCT__GTTTTTTTTAATTTTTTGTAGAGATGGGTCT CAT C EXOSC10 Ensembl:ENSG00000171824 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1286238208 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_98158,RMVar_hsa_circ_4265,RMVar_hsa_circ_83091,RMVar_hsa_circ_8396,RMVar_hsa_circ_129043,RMVar_hsa_circ_106658,RMVar_hsa_circ_127325,RMVar_hsa_circ_129044,RMVar_hsa_circ_121445,RMVar_hsa_circ_129047,RMVar_hsa_circ_129048,RMVar_hsa_circ_23013,RMVar_hsa_circ_129046,RMVar_hsa_circ_129055,RMVar_hsa_circ_315026,RMVar_hsa_circ_371127,RMVar_hsa_circ_129056,RMVar_hsa_circ_22532 12817 RMVar_ID_12817 Human_SNP_ID_3041739 A-to-I Human chr1 - 11078127 11078127 11078127 GGGACCACAGGCATACACCACCATACCCAGCTATGTTTTTTTTAATTTTTTGTAGAGATGGGTCT GGGACCACAGGCATACACCACCATACCCAGCTGTGTTTTTTTTAATTTTTTGTAGAGATGGGTCT T C EXOSC10 Ensembl:ENSG00000171824 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs980746029 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98158,RMVar_hsa_circ_4265,RMVar_hsa_circ_83091,RMVar_hsa_circ_8396,RMVar_hsa_circ_129043,RMVar_hsa_circ_106658,RMVar_hsa_circ_127325,RMVar_hsa_circ_129044,RMVar_hsa_circ_121445,RMVar_hsa_circ_129047,RMVar_hsa_circ_129048,RMVar_hsa_circ_23013,RMVar_hsa_circ_129046,RMVar_hsa_circ_129055,RMVar_hsa_circ_315026,RMVar_hsa_circ_371127,RMVar_hsa_circ_129056,RMVar_hsa_circ_22532 12818 RMVar_ID_12818 Human_SNP_ID_3041751 A-to-I Human chr1 - 11078180 11078180 11078180 GCTCACTGTAGCCTCGCATCTGCTAGGCTCCCACCTTAGCCTCCTGAGCAGCTGGGACCACAGGC GCTCACTGTAGCCTCGCATCTGCTAGGCTCCCCCCTTAGCCTCCTGAGCAGCTGGGACCACAGGC T G EXOSC10 Ensembl:ENSG00000171824 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913706250 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10516726 RMVar_hsa_circ_98158,RMVar_hsa_circ_4265,RMVar_hsa_circ_83091,RMVar_hsa_circ_8396,RMVar_hsa_circ_129043,RMVar_hsa_circ_106658,RMVar_hsa_circ_127325,RMVar_hsa_circ_129044,RMVar_hsa_circ_121445,RMVar_hsa_circ_129047,RMVar_hsa_circ_129048,RMVar_hsa_circ_23013,RMVar_hsa_circ_129046,RMVar_hsa_circ_129055,RMVar_hsa_circ_315026,RMVar_hsa_circ_371127,RMVar_hsa_circ_129056,RMVar_hsa_circ_22532 12819 RMVar_ID_12819 Human_SNP_ID_3041779 A-to-I Human chr1 - 11078259 11078259 11078259 AGCGAGACTCCGTCTCAAAAAAAAAAAGAAACAGGGTCTTGCTCTGACACCCAGGCTGGAGTGCA AGCGAGACTCCGTCTCAAAAAAAAAAAGAAACGGGGTCTTGCTCTGACACCCAGGCTGGAGTGCA T C EXOSC10 Ensembl:ENSG00000171824 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1450911550 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98158,RMVar_hsa_circ_4265,RMVar_hsa_circ_83091,RMVar_hsa_circ_8396,RMVar_hsa_circ_129043,RMVar_hsa_circ_106658,RMVar_hsa_circ_127325,RMVar_hsa_circ_129044,RMVar_hsa_circ_121445,RMVar_hsa_circ_129047,RMVar_hsa_circ_129048,RMVar_hsa_circ_23013,RMVar_hsa_circ_129046,RMVar_hsa_circ_129055,RMVar_hsa_circ_315026,RMVar_hsa_circ_371127,RMVar_hsa_circ_129056,RMVar_hsa_circ_22532 12820 RMVar_ID_12820 Human_SNP_ID_3042208 A-to-I Human chr1 - 11079669 11079669 11079669 TTTTCTGCGGCTGGGCACAGTGGCTCACGCCTATAATCTCAGCACTTTGGGAGGCTGAGGTGGCT TTTTCTGCGGCTGGGCACAGTGGCTCACGCCTGTAATCTCAGCACTTTGGGAGGCTGAGGTGGCT T C EXOSC10 Ensembl:ENSG00000171824 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs768172287 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98158,RMVar_hsa_circ_4265,RMVar_hsa_circ_83091,RMVar_hsa_circ_8396,RMVar_hsa_circ_129043,RMVar_hsa_circ_106658,RMVar_hsa_circ_127325,RMVar_hsa_circ_129044,RMVar_hsa_circ_121445,RMVar_hsa_circ_129047,RMVar_hsa_circ_129048,RMVar_hsa_circ_23013,RMVar_hsa_circ_129046,RMVar_hsa_circ_129055,RMVar_hsa_circ_315026,RMVar_hsa_circ_371127,RMVar_hsa_circ_129056,RMVar_hsa_circ_22532 12821 RMVar_ID_12821 Human_SNP_ID_3043263 A-to-I Human chr1 - 11083089 11083089 11083089 CCAAAGTTTAGCTGGGCGTGGTGGCACGCTGTAGTCCCAACTACTTGGGAGGCTGAGGTGGGAGG CCAAAGTTTAGCTGGGCGTGGTGGCACGCTGTGGTCCCAACTACTTGGGAGGCTGAGGTGGGAGG T C EXOSC10 Ensembl:ENSG00000171824 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900929962 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24571419 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_129047,RMVar_hsa_circ_129048,RMVar_hsa_circ_129046,RMVar_hsa_circ_15609,RMVar_hsa_circ_94386,RMVar_hsa_circ_129058 12822 RMVar_ID_12822 Human_SNP_ID_3052352 A-to-I Human chr1 - 11117298 11117298 11117298 AAATAAGCTGGGCATGGTGGCGGGTGCCTGTAATCTCAGCTACTCAGGAGGCTGAGGCATGAGAA AAATAAGCTGGGCATGGTGGCGGGTGCCTGTAGTCTCAGCTACTCAGGAGGCTGAGGCATGAGAA T C MTOR Ensembl:ENSG00000198793 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1243518674 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1741,RMVar_hsa_circ_98592,RMVar_hsa_circ_102553,RMVar_hsa_circ_129068,RMVar_hsa_circ_98908,RMVar_hsa_circ_129067,RMVar_hsa_circ_100586,RMVar_hsa_circ_370450,RMVar_hsa_circ_129069,RMVar_hsa_circ_129073,RMVar_hsa_circ_87622,RMVar_hsa_circ_129074,RMVar_hsa_circ_129072,RMVar_hsa_circ_52865,RMVar_hsa_circ_75310,RMVar_hsa_circ_90661,RMVar_hsa_circ_86561,RMVar_hsa_circ_119004,RMVar_hsa_circ_129075,RMVar_hsa_circ_129076,RMVar_hsa_circ_129077,RMVar_hsa_circ_327456,RMVar_hsa_circ_121812,RMVar_hsa_circ_54709,RMVar_hsa_circ_123133,RMVar_hsa_circ_129079,RMVar_hsa_circ_129080,RMVar_hsa_circ_89666,RMVar_hsa_circ_106703,RMVar_hsa_circ_129081,RMVar_hsa_circ_129082,RMVar_hsa_circ_129083,RMVar_hsa_circ_122585,RMVar_hsa_circ_129084,RMVar_hsa_circ_2864,RMVar_hsa_circ_84396,RMVar_hsa_circ_129085,RMVar_hsa_circ_129086 12823 RMVar_ID_12823 Human_SNP_ID_3052353 A-to-I Human chr1 - 11117298 11117298 11117298 AAATAAGCTGGGCATGGTGGCGGGTGCCTGTAATCTCAGCTACTCAGGAGGCTGAGGCATGAGAA AAATAAGCTGGGCATGGTGGCGGGTGCCTGTACTCTCAGCTACTCAGGAGGCTGAGGCATGAGAA T G MTOR Ensembl:ENSG00000198793 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1243518674 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1741,RMVar_hsa_circ_98592,RMVar_hsa_circ_102553,RMVar_hsa_circ_129068,RMVar_hsa_circ_98908,RMVar_hsa_circ_129067,RMVar_hsa_circ_100586,RMVar_hsa_circ_370450,RMVar_hsa_circ_129069,RMVar_hsa_circ_129073,RMVar_hsa_circ_87622,RMVar_hsa_circ_129074,RMVar_hsa_circ_129072,RMVar_hsa_circ_52865,RMVar_hsa_circ_75310,RMVar_hsa_circ_90661,RMVar_hsa_circ_86561,RMVar_hsa_circ_119004,RMVar_hsa_circ_129075,RMVar_hsa_circ_129076,RMVar_hsa_circ_129077,RMVar_hsa_circ_327456,RMVar_hsa_circ_121812,RMVar_hsa_circ_54709,RMVar_hsa_circ_123133,RMVar_hsa_circ_129079,RMVar_hsa_circ_129080,RMVar_hsa_circ_89666,RMVar_hsa_circ_106703,RMVar_hsa_circ_129081,RMVar_hsa_circ_129082,RMVar_hsa_circ_129083,RMVar_hsa_circ_122585,RMVar_hsa_circ_129084,RMVar_hsa_circ_2864,RMVar_hsa_circ_84396,RMVar_hsa_circ_129085,RMVar_hsa_circ_129086 12824 RMVar_ID_12824 Human_SNP_ID_3052708 A-to-I Human chr1 - 11118583 11118583 11118583 GAAGAAAAAGACCACACCTATGAAAAGCCATTACACTCCAGCCTGGGTAATATAGTGAGATCGTC GAAGAAAAAGACCACACCTATGAAAAGCCATTGCACTCCAGCCTGGGTAATATAGTGAGATCGTC T C MTOR Ensembl:ENSG00000198793 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886728993 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1741,RMVar_hsa_circ_98592,RMVar_hsa_circ_102553,RMVar_hsa_circ_129068,RMVar_hsa_circ_98908,RMVar_hsa_circ_129067,RMVar_hsa_circ_100586,RMVar_hsa_circ_370450,RMVar_hsa_circ_129069,RMVar_hsa_circ_129073,RMVar_hsa_circ_87622,RMVar_hsa_circ_129074,RMVar_hsa_circ_129072,RMVar_hsa_circ_52865,RMVar_hsa_circ_75310,RMVar_hsa_circ_90661,RMVar_hsa_circ_86561,RMVar_hsa_circ_119004,RMVar_hsa_circ_129075,RMVar_hsa_circ_129076,RMVar_hsa_circ_129077,RMVar_hsa_circ_327456,RMVar_hsa_circ_121812,RMVar_hsa_circ_54709,RMVar_hsa_circ_123133,RMVar_hsa_circ_129079,RMVar_hsa_circ_129080,RMVar_hsa_circ_89666,RMVar_hsa_circ_106703,RMVar_hsa_circ_129081,RMVar_hsa_circ_129082,RMVar_hsa_circ_129083,RMVar_hsa_circ_122585,RMVar_hsa_circ_129084,RMVar_hsa_circ_2864,RMVar_hsa_circ_84396,RMVar_hsa_circ_129085,RMVar_hsa_circ_129086 12825 RMVar_ID_12825 Human_SNP_ID_3052709 A-to-I Human chr1 - 11118583 11118583 11118583 GAAGAAAAAGACCACACCTATGAAAAGCCATTACACTCCAGCCTGGGTAATATAGTGAGATCGTC GAAGAAAAAGACCACACCTATGAAAAGCCATTCCACTCCAGCCTGGGTAATATAGTGAGATCGTC T G MTOR Ensembl:ENSG00000198793 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886728993 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1741,RMVar_hsa_circ_98592,RMVar_hsa_circ_102553,RMVar_hsa_circ_129068,RMVar_hsa_circ_98908,RMVar_hsa_circ_129067,RMVar_hsa_circ_100586,RMVar_hsa_circ_370450,RMVar_hsa_circ_129069,RMVar_hsa_circ_129073,RMVar_hsa_circ_87622,RMVar_hsa_circ_129074,RMVar_hsa_circ_129072,RMVar_hsa_circ_52865,RMVar_hsa_circ_75310,RMVar_hsa_circ_90661,RMVar_hsa_circ_86561,RMVar_hsa_circ_119004,RMVar_hsa_circ_129075,RMVar_hsa_circ_129076,RMVar_hsa_circ_129077,RMVar_hsa_circ_327456,RMVar_hsa_circ_121812,RMVar_hsa_circ_54709,RMVar_hsa_circ_123133,RMVar_hsa_circ_129079,RMVar_hsa_circ_129080,RMVar_hsa_circ_89666,RMVar_hsa_circ_106703,RMVar_hsa_circ_129081,RMVar_hsa_circ_129082,RMVar_hsa_circ_129083,RMVar_hsa_circ_122585,RMVar_hsa_circ_129084,RMVar_hsa_circ_2864,RMVar_hsa_circ_84396,RMVar_hsa_circ_129085,RMVar_hsa_circ_129086 12826 RMVar_ID_12826 Human_SNP_ID_3053057 A-to-I Human chr1 - 11119732 11119732 11119732 TGTTTTGTTTTTTTTTTTTGAGACAAGGTCTTACTCTGTTACCCAGGCTGGAGTGCAGCAGCACG TGTTTTGTTTTTTTTTTTTGAGACAAGGTCTTGCTCTGTTACCCAGGCTGGAGTGCAGCAGCACG T C MTOR Ensembl:ENSG00000198793 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1441531401 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1741,RMVar_hsa_circ_98592,RMVar_hsa_circ_102553,RMVar_hsa_circ_129068,RMVar_hsa_circ_98908,RMVar_hsa_circ_129067,RMVar_hsa_circ_100586,RMVar_hsa_circ_370450,RMVar_hsa_circ_129069,RMVar_hsa_circ_129073,RMVar_hsa_circ_87622,RMVar_hsa_circ_129074,RMVar_hsa_circ_129072,RMVar_hsa_circ_52865,RMVar_hsa_circ_75310,RMVar_hsa_circ_90661,RMVar_hsa_circ_86561,RMVar_hsa_circ_119004,RMVar_hsa_circ_129075,RMVar_hsa_circ_129076,RMVar_hsa_circ_129077,RMVar_hsa_circ_327456,RMVar_hsa_circ_121812,RMVar_hsa_circ_54709,RMVar_hsa_circ_123133,RMVar_hsa_circ_129079,RMVar_hsa_circ_129080,RMVar_hsa_circ_89666,RMVar_hsa_circ_106703,RMVar_hsa_circ_129081,RMVar_hsa_circ_129082,RMVar_hsa_circ_129083,RMVar_hsa_circ_122585,RMVar_hsa_circ_129084,RMVar_hsa_circ_2864,RMVar_hsa_circ_84396,RMVar_hsa_circ_129085,RMVar_hsa_circ_129086 12827 RMVar_ID_12827 Human_SNP_ID_3053060 A-to-I Human chr1 - 11119739 11119739 11119739 TGTGTTTTGTTTTGTTTTTTTTTTTTGAGACAAGGTCTTACTCTGTTACCCAGGCTGGAGTGCAG TGTGTTTTGTTTTGTTTTTTTTTTTTGAGACAGGGTCTTACTCTGTTACCCAGGCTGGAGTGCAG T C MTOR Ensembl:ENSG00000198793 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1436223495 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1741,RMVar_hsa_circ_98592,RMVar_hsa_circ_102553,RMVar_hsa_circ_129068,RMVar_hsa_circ_98908,RMVar_hsa_circ_129067,RMVar_hsa_circ_100586,RMVar_hsa_circ_370450,RMVar_hsa_circ_129069,RMVar_hsa_circ_129073,RMVar_hsa_circ_87622,RMVar_hsa_circ_129074,RMVar_hsa_circ_129072,RMVar_hsa_circ_52865,RMVar_hsa_circ_75310,RMVar_hsa_circ_90661,RMVar_hsa_circ_86561,RMVar_hsa_circ_119004,RMVar_hsa_circ_129075,RMVar_hsa_circ_129076,RMVar_hsa_circ_129077,RMVar_hsa_circ_327456,RMVar_hsa_circ_121812,RMVar_hsa_circ_54709,RMVar_hsa_circ_123133,RMVar_hsa_circ_129079,RMVar_hsa_circ_129080,RMVar_hsa_circ_89666,RMVar_hsa_circ_106703,RMVar_hsa_circ_129081,RMVar_hsa_circ_129082,RMVar_hsa_circ_129083,RMVar_hsa_circ_122585,RMVar_hsa_circ_129084,RMVar_hsa_circ_2864,RMVar_hsa_circ_84396,RMVar_hsa_circ_129085,RMVar_hsa_circ_129086 12828 RMVar_ID_12828 Human_SNP_ID_3053243 A-to-I Human chr1 - 11120356 11120356 11120356 TTTTGTATTCTTAGTAGAGACAGGGTTTCACCATGTTGTCCAGGCTAGTCTCAAACTCCTGACCT TTTTGTATTCTTAGTAGAGACAGGGTTTCACCGTGTTGTCCAGGCTAGTCTCAAACTCCTGACCT T C MTOR Ensembl:ENSG00000198793 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs751164996 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1741,RMVar_hsa_circ_98592,RMVar_hsa_circ_102553,RMVar_hsa_circ_129068,RMVar_hsa_circ_98908,RMVar_hsa_circ_129067,RMVar_hsa_circ_100586,RMVar_hsa_circ_370450,RMVar_hsa_circ_129069,RMVar_hsa_circ_129073,RMVar_hsa_circ_87622,RMVar_hsa_circ_129074,RMVar_hsa_circ_129072,RMVar_hsa_circ_52865,RMVar_hsa_circ_75310,RMVar_hsa_circ_90661,RMVar_hsa_circ_86561,RMVar_hsa_circ_119004,RMVar_hsa_circ_129075,RMVar_hsa_circ_129076,RMVar_hsa_circ_129077,RMVar_hsa_circ_327456,RMVar_hsa_circ_121812,RMVar_hsa_circ_54709,RMVar_hsa_circ_123133,RMVar_hsa_circ_129079,RMVar_hsa_circ_129080,RMVar_hsa_circ_89666,RMVar_hsa_circ_106703,RMVar_hsa_circ_129081,RMVar_hsa_circ_129082,RMVar_hsa_circ_129083,RMVar_hsa_circ_122585,RMVar_hsa_circ_129084,RMVar_hsa_circ_2864,RMVar_hsa_circ_84396,RMVar_hsa_circ_129085,RMVar_hsa_circ_129086 12829 RMVar_ID_12829 Human_SNP_ID_3053247 A-to-I Human chr1 - 11120367 11120367 11120367 TGTGGGTTAATTTTTGTATTCTTAGTAGAGACAGGGTTTCACCATGTTGTCCAGGCTAGTCTCAA TGTGGGTTAATTTTTGTATTCTTAGTAGAGACGGGGTTTCACCATGTTGTCCAGGCTAGTCTCAA T C MTOR Ensembl:ENSG00000198793 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs889142773 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1741,RMVar_hsa_circ_98592,RMVar_hsa_circ_102553,RMVar_hsa_circ_129068,RMVar_hsa_circ_98908,RMVar_hsa_circ_129067,RMVar_hsa_circ_100586,RMVar_hsa_circ_370450,RMVar_hsa_circ_129069,RMVar_hsa_circ_129073,RMVar_hsa_circ_87622,RMVar_hsa_circ_129074,RMVar_hsa_circ_129072,RMVar_hsa_circ_52865,RMVar_hsa_circ_75310,RMVar_hsa_circ_90661,RMVar_hsa_circ_86561,RMVar_hsa_circ_119004,RMVar_hsa_circ_129075,RMVar_hsa_circ_129076,RMVar_hsa_circ_129077,RMVar_hsa_circ_327456,RMVar_hsa_circ_121812,RMVar_hsa_circ_54709,RMVar_hsa_circ_123133,RMVar_hsa_circ_129079,RMVar_hsa_circ_129080,RMVar_hsa_circ_89666,RMVar_hsa_circ_106703,RMVar_hsa_circ_129081,RMVar_hsa_circ_129082,RMVar_hsa_circ_129083,RMVar_hsa_circ_122585,RMVar_hsa_circ_129084,RMVar_hsa_circ_2864,RMVar_hsa_circ_84396,RMVar_hsa_circ_129085,RMVar_hsa_circ_129086 12830 RMVar_ID_12830 Human_SNP_ID_3095544 A-to-I Human chr1 + 11288674 11288674 11288674 TCACGCTTGTAATCACAGTAATTTGTGAGGCCAAGGTGAGAGGATTGCTTGAGCCCAGGAGTTTG TCACGCTTGTAATCACAGTAATTTGTGAGGCCGAGGTGAGAGGATTGCTTGAGCCCAGGAGTTTG A G UBIAD1 Ensembl:ENSG00000120942 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs183047101 Functional Loss SNV dbSNP153 33..33 33 - - - 12831 RMVar_ID_12831 Human_SNP_ID_3096231 A-to-I Human chr1 + 11291513 11291513 11291513 ACTGTAATCCCAGCGACTCGGGAGGCTGAGGCAGGAGAACTACCTGAACCCGGGAGGCAGAGATT ACTGTAATCCCAGCGACTCGGGAGGCTGAGGCGGGAGAACTACCTGAACCCGGGAGGCAGAGATT A G UBIAD1 Ensembl:ENSG00000120942 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1173174394 Functional Loss SNV dbSNP153 33..33 33 - - - 12832 RMVar_ID_12832 Human_SNP_ID_3229901 A-to-I Human chr1 - 11796936 11796936 11796936 CCTTGGCCTCCCAAAGTGCTGGGATTACAGACATGAGCCACCGCACCCTGCCATCCATTATTTTC CCTTGGCCTCCCAAAGTGCTGGGATTACAGACGTGAGCCACCGCACCCTGCCATCCATTATTTTC T C MTHFR Ensembl:ENSG00000177000 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1231429316 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7831,RMVar_hsa_circ_62604,RMVar_hsa_circ_24829,RMVar_hsa_circ_129190,RMVar_hsa_circ_283781,RMVar_hsa_circ_323530 12833 RMVar_ID_12833 Human_SNP_ID_3230039 A-to-I Human chr1 - 11797431 11797431 11797431 TTAATTAGCCAGATGTGGTGGCTTGCATCTGTAGTCCAAGCTACTCAGGAGACTGAAGTGGGAGA TTAATTAGCCAGATGTGGTGGCTTGCATCTGTGGTCCAAGCTACTCAGGAGACTGAAGTGGGAGA T C MTHFR Ensembl:ENSG00000177000 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1051824431 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7831,RMVar_hsa_circ_62604,RMVar_hsa_circ_24829,RMVar_hsa_circ_129190,RMVar_hsa_circ_283781,RMVar_hsa_circ_323530 12834 RMVar_ID_12834 Human_SNP_ID_3233001 A-to-I Human chr1 + 11807888 11807888 11807888 AGTAACAAAAATGAGATTCCACTAAATCATCTATTTTAACCTGTCCCACTCACCCCCTTTATTAT AGTAACAAAAATGAGATTCCACTAAATCATCTTTTTTAACCTGTCCCACTCACCCCCTTTATTAT A T CLCN6 Ensembl:ENSG00000011021 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1004595715 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17723087 12835 RMVar_ID_12835 Human_SNP_ID_3233345 A-to-I Human chr1 + 11808955 11808955 11808955 ATCTCAGCTCACTGCAACCTCCACCCCACCCTAGGTTCAAGCGGTTCTTCTGCCCCAGCCTCCCG ATCTCAGCTCACTGCAACCTCCACCCCACCCTCGGTTCAAGCGGTTCTTCTGCCCCAGCCTCCCG A C CLCN6 Ensembl:ENSG00000011021 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs766162703 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10544571 12836 RMVar_ID_12836 Human_SNP_ID_3233615 A-to-I Human chr1 + 11809974 11809974 11809974 TAAAGAGGGGAGTGAGTGGGACAGGTTAAAATAGTTGATTTAGTGGAATCTCATTTTTGTTATTT TAAAGAGGGGAGTGAGTGGGACAGGTTAAAATTGTTGATTTAGTGGAATCTCATTTTTGTTATTT A T CLCN6 Ensembl:ENSG00000011021 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1385251496 Functional Loss SNV dbSNP153 33..33 33 - - - 12837 RMVar_ID_12837 Human_SNP_ID_3233815 A-to-I Human chr1 + 11810808 11810808 11810808 AAAAAAGAAGCGTGGCACAGTGGCTCACGCCTATATGCTCAGCACTTTGGGAGGCCAAGGCAGGA AAAAAAGAAGCGTGGCACAGTGGCTCACGCCTGTATGCTCAGCACTTTGGGAGGCCAAGGCAGGA A G CLCN6 Ensembl:ENSG00000011021 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1382857688 Functional Loss SNV dbSNP153 33..33 33 - - - 12838 RMVar_ID_12838 Human_SNP_ID_3234624 A-to-I Human chr1 + 11813574 11813574 11813574 CACCACACCCACCTAATTTGTGTATTTTTGGTAGAGACGGGGTTTCGCCATGTTGGCCGGGCTGG CACCACACCCACCTAATTTGTGTATTTTTGGTGGAGACGGGGTTTCGCCATGTTGGCCGGGCTGG A G CLCN6 Ensembl:ENSG00000011021 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1408457753 Functional Loss SNV dbSNP153 33..33 33 - - - 12839 RMVar_ID_12839 Human_SNP_ID_3234847 A-to-I Human chr1 + 11814411 11814411 11814411 AGCTGGGATTACAGGCGTGCTCCACCACTCCCAGCTAACTTGTATTTTTAGTAGAGATGGGGTTT AGCTGGGATTACAGGCGTGCTCCACCACTCCCGGCTAACTTGTATTTTTAGTAGAGATGGGGTTT A G CLCN6 Ensembl:ENSG00000011021 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs994106310 Functional Loss SNV dbSNP153 33..33 33 - - - 12840 RMVar_ID_12840 Human_SNP_ID_3234851 A-to-I Human chr1 + 11814448 11814448 11814448 ACTTGTATTTTTAGTAGAGATGGGGTTTCACCATCTTGCCTAGGCTGGTCTCGAACTTCTGGCCT ACTTGTATTTTTAGTAGAGATGGGGTTTCACCCTCTTGCCTAGGCTGGTCTCGAACTTCTGGCCT A C CLCN6 Ensembl:ENSG00000011021 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1027820276 Functional Loss SNV dbSNP153 33..33 33 - - - 12841 RMVar_ID_12841 Human_SNP_ID_3234852 A-to-I Human chr1 + 11814448 11814448 11814448 ACTTGTATTTTTAGTAGAGATGGGGTTTCACCATCTTGCCTAGGCTGGTCTCGAACTTCTGGCCT ACTTGTATTTTTAGTAGAGATGGGGTTTCACCGTCTTGCCTAGGCTGGTCTCGAACTTCTGGCCT A G CLCN6 Ensembl:ENSG00000011021 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1027820276 Functional Loss SNV dbSNP153 33..33 33 - - - 12842 RMVar_ID_12842 Human_SNP_ID_3237007 A-to-I Human chr1 + 11822504 11822504 11822504 GGCTCAAGTGATCCTCCTGCCTCAGCCTCCCAAAGTGTTGGGATTACAGGCATGAGCCATTGCAC GGCTCAAGTGATCCTCCTGCCTCAGCCTCCCAGAGTGTTGGGATTACAGGCATGAGCCATTGCAC A G CLCN6 Ensembl:ENSG00000011021 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs901863457 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17442,RMVar_hsa_circ_364085,RMVar_hsa_circ_369676,RMVar_hsa_circ_129194 12843 RMVar_ID_12843 Human_SNP_ID_3272387 A-to-I Human chr1 + 11942217 11942217 11942217 GTTGGCCAGGCTGGTCTCAAATTTCTGATCTCAACTGATCTGCCTGCCTCAGCTTCCCCTCACTT GTTGGCCAGGCTGGTCTCAAATTTCTGATCTCGACTGATCTGCCTGCCTCAGCTTCCCCTCACTT A G PLOD1 Ensembl:ENSG00000083444 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs973609732 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77725,RMVar_hsa_circ_126101,RMVar_hsa_circ_129208,RMVar_hsa_circ_129209 12844 RMVar_ID_12844 Human_SNP_ID_3272676 A-to-I Human chr1 + 11943477 11943477 11943477 TGCCACCACGCCCGGCTAATTTTTGTATTCTTAGTAGAGACAGGGTTTCACCATGTTGACCAGGC TGCCACCACGCCCGGCTAATTTTTGTATTCTTGGTAGAGACAGGGTTTCACCATGTTGACCAGGC A G PLOD1 Ensembl:ENSG00000083444 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1237489679 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77725,RMVar_hsa_circ_126101,RMVar_hsa_circ_129208,RMVar_hsa_circ_129209,RMVar_hsa_circ_129210 12845 RMVar_ID_12845 Human_SNP_ID_3275464 A-to-I Human chr1 + 11953608 11953608 11953608 GAGGTCAGGAGTTTGAGACCAGCCTGGCCAACATGATGAAACCCTGTCTCTACTAAAAATATAAA GAGGTCAGGAGTTTGAGACCAGCCTGGCCAACGTGATGAAACCCTGTCTCTACTAAAAATATAAA A G PLOD1 Ensembl:ENSG00000083444 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1268043589 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81636,RMVar_hsa_circ_77725,RMVar_hsa_circ_126101,RMVar_hsa_circ_129208,RMVar_hsa_circ_129209,RMVar_hsa_circ_79810,RMVar_hsa_circ_129213,RMVar_hsa_circ_116444,RMVar_hsa_circ_129211,RMVar_hsa_circ_369971,RMVar_hsa_circ_51409,RMVar_hsa_circ_101170,RMVar_hsa_circ_129214,RMVar_hsa_circ_129215,RMVar_hsa_circ_122162,RMVar_hsa_circ_92214,RMVar_hsa_circ_85330,RMVar_hsa_circ_107722,RMVar_hsa_circ_112486,RMVar_hsa_circ_129217,RMVar_hsa_circ_129218,RMVar_hsa_circ_129216,RMVar_hsa_circ_129220,RMVar_hsa_circ_87402,RMVar_hsa_circ_129219,RMVar_hsa_circ_86782,RMVar_hsa_circ_42622,RMVar_hsa_circ_82250,RMVar_hsa_circ_129221,RMVar_hsa_circ_129223,RMVar_hsa_circ_129224,RMVar_hsa_circ_129222 12846 RMVar_ID_12846 Human_SNP_ID_3281944 A-to-I Human chr1 + 11975657 11975643 11975658 TTTTTTTTTTTCTTTTTTTGAGACAGAGTCTCACTCTGTCTTCCAGGCTGGAGTGCAATGACGCT TTTTTTTTTTTCTTTTTTT_______________TCTGTCTTCCAGGCTGGAGTGCAATGACGCT TGAGACAGAGTCTCAC T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1473051026 Functional Loss DEL dbSNP153 20..34 33 - - - 12847 RMVar_ID_12847 Human_SNP_ID_3281970 A-to-I Human chr1 + 11975725 11975725 11975725 CCCGCTTTCTGCAACCCCCGCCTCCTGGGTTCAAGTAATTCTCCTGCCTCAGCCTTCCGAGCAGC CCCGCTTTCTGCAACCCCCGCCTCCTGGGTTCGAGTAATTCTCCTGCCTCAGCCTTCCGAGCAGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917347168 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26367002 12848 RMVar_ID_12848 Human_SNP_ID_3281997 A-to-I Human chr1 + 11975826 11975826 11975826 TTTTGTTTTTTTATTAAAGAAAGGGTTTCACCAGGTTGGTCTGGCTGGTCTTGAACTCCTGACCT TTTTGTTTTTTTATTAAAGAAAGGGTTTCACCGGGTTGGTCTGGCTGGTCTTGAACTCCTGACCT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs377576180 Functional Loss SNV dbSNP153 33..33 33 - - - 12849 RMVar_ID_12849 Human_SNP_ID_3282138 A-to-I Human chr1 + 11976349 11976349 11976349 GGTTGTGTTGGCATGCGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAA GGTTGTGTTGGCATGCGCCTGTAATCCCAGCTCCTCGGGAGGCTGAGGCAGGAGAATCGCTTGAA A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1212658469 Functional Loss SNV dbSNP153 33..33 33 - - - 12850 RMVar_ID_12850 Human_SNP_ID_3282139 A-to-I Human chr1 + 11976349 11976349 11976349 GGTTGTGTTGGCATGCGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAA GGTTGTGTTGGCATGCGCCTGTAATCCCAGCTGCTCGGGAGGCTGAGGCAGGAGAATCGCTTGAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1212658469 Functional Loss SNV dbSNP153 33..33 33 - - - 12851 RMVar_ID_12851 Human_SNP_ID_3284019 A-to-I Human chr1 + 11983177 11983177 11983177 TCACTGCAAGCTCTGCCTCCCAGGTTCACACTATCCTCCTGCCTCAGCCTCCCGAGTAGCTGTAC TCACTGCAAGCTCTGCCTCCCAGGTTCACACTCTCCTCCTGCCTCAGCCTCCCGAGTAGCTGTAC A C MFN2 Ensembl:ENSG00000116688 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs977120742 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88951,RMVar_hsa_circ_121432,RMVar_hsa_circ_25321,RMVar_hsa_circ_129240,RMVar_hsa_circ_129241,RMVar_hsa_circ_358774,RMVar_hsa_circ_368564 12852 RMVar_ID_12852 Human_SNP_ID_3284020 A-to-I Human chr1 + 11983177 11983177 11983177 TCACTGCAAGCTCTGCCTCCCAGGTTCACACTATCCTCCTGCCTCAGCCTCCCGAGTAGCTGTAC TCACTGCAAGCTCTGCCTCCCAGGTTCACACTGTCCTCCTGCCTCAGCCTCCCGAGTAGCTGTAC A G MFN2 Ensembl:ENSG00000116688 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs977120742 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88951,RMVar_hsa_circ_121432,RMVar_hsa_circ_25321,RMVar_hsa_circ_129240,RMVar_hsa_circ_129241,RMVar_hsa_circ_358774,RMVar_hsa_circ_368564 12853 RMVar_ID_12853 Human_SNP_ID_3284864 A-to-I Human chr1 + 11986732 11986732 11986732 CGTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGTGCCTGCCACCATGCCTGGCTAATTTTTGT CGTGCCTCAGCCTCCCGAGTAGCTGGGATTACGGGTGCCTGCCACCATGCCTGGCTAATTTTTGT A G MFN2 Ensembl:ENSG00000116688 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs538604359 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88951,RMVar_hsa_circ_121432,RMVar_hsa_circ_25321,RMVar_hsa_circ_129240,RMVar_hsa_circ_129241,RMVar_hsa_circ_358774,RMVar_hsa_circ_368564 12854 RMVar_ID_12854 Human_SNP_ID_3285047 A-to-I Human chr1 + 11987428 11987428 11987428 AAGGTGGGTGGATCATTTGAGGTCAGGAGTTCAAGACCTACCTGGCCAACATGGTGAAACCCCAC AAGGTGGGTGGATCATTTGAGGTCAGGAGTTCCAGACCTACCTGGCCAACATGGTGAAACCCCAC A C MFN2 Ensembl:ENSG00000116688 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1309527087 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88951,RMVar_hsa_circ_121432,RMVar_hsa_circ_25321,RMVar_hsa_circ_129240,RMVar_hsa_circ_129241,RMVar_hsa_circ_358774,RMVar_hsa_circ_368564 12855 RMVar_ID_12855 Human_SNP_ID_3286526 A-to-I Human chr1 + 11992847 11992847 11992847 TATATTTTATTTATTTATTTGATTTTTGAGACAGGGTTCTCTGTCACCCAGGCTGGAAGCTCATT TATATTTTATTTATTTATTTGATTTTTGAGACCGGGTTCTCTGTCACCCAGGCTGGAAGCTCATT A C MFN2 Ensembl:ENSG00000116688 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1247851842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5680733 RMVar_hsa_circ_53003,RMVar_hsa_circ_88951,RMVar_hsa_circ_121432,RMVar_hsa_circ_81796,RMVar_hsa_circ_25321,RMVar_hsa_circ_129240,RMVar_hsa_circ_129241,RMVar_hsa_circ_358774,RMVar_hsa_circ_370908,RMVar_hsa_circ_375557,RMVar_hsa_circ_281980,RMVar_hsa_circ_119051,RMVar_hsa_circ_129245,RMVar_hsa_circ_129247,RMVar_hsa_circ_129248,RMVar_hsa_circ_129246,RMVar_hsa_circ_129244,RMVar_hsa_circ_89892,RMVar_hsa_circ_129249 12856 RMVar_ID_12856 Human_SNP_ID_3288530 A-to-I Human chr1 + 12000057 12000057 12000057 AGGTGGAGCTTGCAGTGAGCTGAGATTGTGCCACTGTACTCCAGCCTGGGCAAGAGAGTGAGATT AGGTGGAGCTTGCAGTGAGCTGAGATTGTGCCCCTGTACTCCAGCCTGGGCAAGAGAGTGAGATT A C MFN2 Ensembl:ENSG00000116688 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1198739732 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10551974,Human_RBP_ID_23143570,Human_RBP_ID_24579176 RMVar_hsa_circ_121432,RMVar_hsa_circ_81796,RMVar_hsa_circ_25321,RMVar_hsa_circ_129241,RMVar_hsa_circ_375557,RMVar_hsa_circ_119051,RMVar_hsa_circ_129247,RMVar_hsa_circ_129248,RMVar_hsa_circ_129246,RMVar_hsa_circ_129254,RMVar_hsa_circ_105721,RMVar_hsa_circ_128117,RMVar_hsa_circ_129256,RMVar_hsa_circ_102887,RMVar_hsa_circ_129255 12857 RMVar_ID_12857 Human_SNP_ID_3295464 A-to-I Human chr1 + 12023229 12023229 12023229 GGGATTACAGGCGAGCACCACCACGCCCGGCTAATTTTTGTATTTTAAGTAGAGATGGGGTTTCC GGGATTACAGGCGAGCACCACCACGCCCGGCTGATTTTTGTATTTTAAGTAGAGATGGGGTTTCC A G MIIP Ensembl:ENSG00000116691 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1448665641 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100336,RMVar_hsa_circ_129268 12858 RMVar_ID_12858 Human_SNP_ID_3295835 A-to-I Human chr1 + 12024469 12024469 12024469 AAGTCTCACTCTTGTCATCCAGGCTAGAGTGCAATGGCGTGATCTCCGCTCACTGCAACCTCCGC AAGTCTCACTCTTGTCATCCAGGCTAGAGTGCGATGGCGTGATCTCCGCTCACTGCAACCTCCGC A G MIIP Ensembl:ENSG00000116691 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1332844936 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100336,RMVar_hsa_circ_129268 12859 RMVar_ID_12859 Human_SNP_ID_3296039 A-to-I Human chr1 + 12025199 12025199 12025199 CTTGTGCCTCAGCCTCCCGAGTAGCAGGTATTACAGGTGTGCGCCACCACACCCAGCTAATTTTT CTTGTGCCTCAGCCTCCCGAGTAGCAGGTATTGCAGGTGTGCGCCACCACACCCAGCTAATTTTT A G MIIP Ensembl:ENSG00000116691 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1461884166 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100336,RMVar_hsa_circ_129268 12860 RMVar_ID_12860 Human_SNP_ID_3296185 A-to-I Human chr1 + 12025837 12025837 12025837 ATTCTTCCTCAGCCTCCCAGGTAGCTGGGATTACAGACGTCCACTACCATGCTTGGCTTATTTTT ATTCTTCCTCAGCCTCCCAGGTAGCTGGGATTGCAGACGTCCACTACCATGCTTGGCTTATTTTT A G MIIP Ensembl:ENSG00000116691 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1451518274 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100336,RMVar_hsa_circ_129268 12861 RMVar_ID_12861 Human_SNP_ID_3296273 A-to-I Human chr1 + 12026230 12026230 12026230 AGGACGCTGAGGCAGGAGAATCATTTGAATCCAGGAAGTGGAGGCTGCAGTGAGCAGAGATCAAG AGGACGCTGAGGCAGGAGAATCATTTGAATCCGGGAAGTGGAGGCTGCAGTGAGCAGAGATCAAG A G MIIP Ensembl:ENSG00000116691 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1430256553 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10552532 RMVar_hsa_circ_100336,RMVar_hsa_circ_129268 12862 RMVar_ID_12862 Human_SNP_ID_3296692 A-to-I Human chr1 + 12027956 12027956 12027956 TGTTTAGGCCGGGTGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGTGG TGTTTAGGCCGGGTGCGGTGGCTCACGCCTGTGATCCCAGCACTTTGGGAGGCCGAGGCAGGTGG A G MIIP Ensembl:ENSG00000116691 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs998615679 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100336,RMVar_hsa_circ_129268 12863 RMVar_ID_12863 Human_SNP_ID_3296740 A-to-I Human chr1 + 12028139 12028139 12028139 TGAGACATGAGAATCGCTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCCGAGGTCGCTCCACTGC TGAGACATGAGAATCGCTTGAACCTGGGAGGCGGAGGTTGCAGTGAGCCGAGGTCGCTCCACTGC A G MIIP Ensembl:ENSG00000116691 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1247147429 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100336,RMVar_hsa_circ_129268 12864 RMVar_ID_12864 Human_SNP_ID_3306971 A-to-I Human chr1 + 12065363 12065363 12065363 TCTCGGCCTCCCAAAGTGCTAGGGTTACAGGCATGAGCCACCACACCCAGCCTCCCATACCCTTT TCTCGGCCTCCCAAAGTGCTAGGGTTACAGGCGTGAGCCACCACACCCAGCCTCCCATACCCTTT A G TNFRSF8 Ensembl:ENSG00000120949 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1457681422 Functional Loss SNV dbSNP153 33..33 33 - - - 12865 RMVar_ID_12865 Human_SNP_ID_3307232 A-to-I Human chr1 + 12066519 12066519 12066519 TGGATTACAGGCACTTGCCATCATGCCTGGCTAATTTTTGTATTTTAGTAGAGATGGGGTTTCAT TGGATTACAGGCACTTGCCATCATGCCTGGCTGATTTTTGTATTTTAGTAGAGATGGGGTTTCAT A G TNFRSF8 Ensembl:ENSG00000120949 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1017212829 Functional Loss SNV dbSNP153 33..33 33 - - - 12866 RMVar_ID_12866 Human_SNP_ID_3308438 A-to-I Human chr1 + 12071318 12071318 12071318 AAAATTAGCCAGGTGTGGCGGTGTGTGCCTGTAGTCCCAGCTACTCGCGAGGTTGAAGCACGAGA AAAATTAGCCAGGTGTGGCGGTGTGTGCCTGTGGTCCCAGCTACTCGCGAGGTTGAAGCACGAGA A G TNFRSF8 Ensembl:ENSG00000120949 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1252726471 Functional Loss SNV dbSNP153 33..33 33 - - - 12867 RMVar_ID_12867 Human_SNP_ID_3308536 A-to-I Human chr1 + 12071705 12071705 12071705 CCTGCCTCAGCCTCCCAAGTAGCTGGGACCACAAGCACCCGCCACCACGCCCGGCTAATTTTTGT CCTGCCTCAGCCTCCCAAGTAGCTGGGACCACGAGCACCCGCCACCACGCCCGGCTAATTTTTGT A G TNFRSF8 Ensembl:ENSG00000120949 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1252223118 Functional Loss SNV dbSNP153 33..33 33 - - - 12868 RMVar_ID_12868 Human_SNP_ID_3308851 A-to-I Human chr1 + 12073132 12073132 12073132 CAACAAAAAATTAGCCGGGCATGGTGGTACACACCTGTGGTCCCAGCTACTCAGGAGGCTGAGGT CAACAAAAAATTAGCCGGGCATGGTGGTACACGCCTGTGGTCCCAGCTACTCAGGAGGCTGAGGT A G TNFRSF8 Ensembl:ENSG00000120949 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1047018519 Functional Loss SNV dbSNP153 33..33 33 - - - 12869 RMVar_ID_12869 Human_SNP_ID_3308858 A-to-I Human chr1 + 12073174 12073174 12073174 CCAGCTACTCAGGAGGCTGAGGTGAGAGGATCACGTGAGCCCAGGAGGTCAAGGCTGTAGTGAGC CCAGCTACTCAGGAGGCTGAGGTGAGAGGATCCCGTGAGCCCAGGAGGTCAAGGCTGTAGTGAGC A C TNFRSF8 Ensembl:ENSG00000120949 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1368959652 Functional Loss SNV dbSNP153 33..33 33 - - - 12870 RMVar_ID_12870 Human_SNP_ID_3308859 A-to-I Human chr1 + 12073174 12073174 12073174 CCAGCTACTCAGGAGGCTGAGGTGAGAGGATCACGTGAGCCCAGGAGGTCAAGGCTGTAGTGAGC CCAGCTACTCAGGAGGCTGAGGTGAGAGGATCGCGTGAGCCCAGGAGGTCAAGGCTGTAGTGAGC A G TNFRSF8 Ensembl:ENSG00000120949 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1368959652 Functional Loss SNV dbSNP153 33..33 33 - - - 12871 RMVar_ID_12871 Human_SNP_ID_3309055 A-to-I Human chr1 + 12073735 12073735 12073735 CCTGCCTCAGGATCCCGAGTAGCTGGGATTACAGGCGCCCACCACCACGCCTGGCTAATTTTTAT CCTGCCTCAGGATCCCGAGTAGCTGGGATTACGGGCGCCCACCACCACGCCTGGCTAATTTTTAT A G TNFRSF8 Ensembl:ENSG00000120949 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs142457042 Functional Loss SNV dbSNP153 33..33 33 - - - 12872 RMVar_ID_12872 Human_SNP_ID_3309074 A-to-I Human chr1 + 12073779 12073779 12073779 CCACGCCTGGCTAATTTTTATGTATTTTTACTAGAGATGGGGTTTCACCATGTTGGCCAAGCTGG CCACGCCTGGCTAATTTTTATGTATTTTTACTGGAGATGGGGTTTCACCATGTTGGCCAAGCTGG A G TNFRSF8 Ensembl:ENSG00000120949 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1428488354 Functional Loss SNV dbSNP153 33..33 33 - - - 12873 RMVar_ID_12873 Human_SNP_ID_3310695 A-to-I Human chr1 + 12080078 12080078 12080078 TCAAGGGATTCTCCCGCCTCAGCCTCCTGAGTAGTTGGGATTACAGGCATGCACCACCATGCCCG TCAAGGGATTCTCCCGCCTCAGCCTCCTGAGTGGTTGGGATTACAGGCATGCACCACCATGCCCG A G TNFRSF8 Ensembl:ENSG00000120949 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1329280524 Functional Loss SNV dbSNP153 33..33 33 - - - 12874 RMVar_ID_12874 Human_SNP_ID_3310817 A-to-I Human chr1 + 12080613 12080613 12080613 GAGTTTCACCCTTGTTGCCTAGGCTGGAGTGCAATGGTGCGTTCTTGGCTCACTGCAGCCTCCAC GAGTTTCACCCTTGTTGCCTAGGCTGGAGTGCGATGGTGCGTTCTTGGCTCACTGCAGCCTCCAC A G TNFRSF8 Ensembl:ENSG00000120949 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1316451452 Functional Loss SNV dbSNP153 33..33 33 - - - 12875 RMVar_ID_12875 Human_SNP_ID_3315752 A-to-I Human chr1 + 12100747 12100747 12100747 GGGAAGCCGAGGTGGGCAGATCACTTGAGGTCAAGAGTTCAAGACCAGCTTGGCCAACATGGTGA GGGAAGCCGAGGTGGGCAGATCACTTGAGGTCCAGAGTTCAAGACCAGCTTGGCCAACATGGTGA A C TNFRSF8 Ensembl:ENSG00000120949 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs896468547 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97325,RMVar_hsa_circ_106252,RMVar_hsa_circ_38726,RMVar_hsa_circ_47296,RMVar_hsa_circ_116530,RMVar_hsa_circ_129269,RMVar_hsa_circ_129270,RMVar_hsa_circ_378710,RMVar_hsa_circ_88555,RMVar_hsa_circ_129271,RMVar_hsa_circ_129272 12876 RMVar_ID_12876 Human_SNP_ID_3316318 A-to-I Human chr1 + 12103217 12103217 12103217 GAAACCCCGTCTCTATAAAAATACAAAAAATTAGTTGGGCGTGGTGGTGTGTGCCTGTAATCCCA GAAACCCCGTCTCTATAAAAATACAAAAAATTCGTTGGGCGTGGTGGTGTGTGCCTGTAATCCCA A C TNFRSF8 Ensembl:ENSG00000120949 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1212849225 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97325,RMVar_hsa_circ_106252,RMVar_hsa_circ_38726,RMVar_hsa_circ_47296,RMVar_hsa_circ_116530,RMVar_hsa_circ_129269,RMVar_hsa_circ_129270,RMVar_hsa_circ_378710,RMVar_hsa_circ_88555,RMVar_hsa_circ_129271,RMVar_hsa_circ_129272 12877 RMVar_ID_12877 Human_SNP_ID_3316429 A-to-I Human chr1 + 12103609 12103609 12103609 CTCCCGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCATGTGCTACCATGCCTGGCTAATTTTT CTCCCGCCTCAGCCTCCCAAGTAGCTGGGACTTCAGGCATGTGCTACCATGCCTGGCTAATTTTT A T TNFRSF8 Ensembl:ENSG00000120949 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1208552374 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97325,RMVar_hsa_circ_106252,RMVar_hsa_circ_38726,RMVar_hsa_circ_47296,RMVar_hsa_circ_116530,RMVar_hsa_circ_129269,RMVar_hsa_circ_129270,RMVar_hsa_circ_378710,RMVar_hsa_circ_88555,RMVar_hsa_circ_129271,RMVar_hsa_circ_129272 12878 RMVar_ID_12878 Human_SNP_ID_3317386 A-to-I Human chr1 + 12107110 12107109 12107110 GTGGCACGTGGCCACGCACTTAAAATGCAGCTAGGGGCCGGGTGCGGTGGCTCACACCTGTAATT GTGGCACGTGGCCACGCACTTAAAATGCAGCT_GGGGCCGGGTGCGGTGGCTCACACCTGTAATT TA T TNFRSF8 Ensembl:ENSG00000120949 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs373970569 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_97325,RMVar_hsa_circ_106252,RMVar_hsa_circ_38726,RMVar_hsa_circ_47296,RMVar_hsa_circ_129269,RMVar_hsa_circ_129270,RMVar_hsa_circ_378710,RMVar_hsa_circ_88555,RMVar_hsa_circ_129272 12879 RMVar_ID_12879 Human_SNP_ID_3317387 A-to-I Human chr1 + 12107110 12107110 12107110 GTGGCACGTGGCCACGCACTTAAAATGCAGCTAGGGGCCGGGTGCGGTGGCTCACACCTGTAATT GTGGCACGTGGCCACGCACTTAAAATGCAGCTGGGGGCCGGGTGCGGTGGCTCACACCTGTAATT A G TNFRSF8 Ensembl:ENSG00000120949 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1172539898 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97325,RMVar_hsa_circ_106252,RMVar_hsa_circ_38726,RMVar_hsa_circ_47296,RMVar_hsa_circ_129269,RMVar_hsa_circ_129270,RMVar_hsa_circ_378710,RMVar_hsa_circ_88555,RMVar_hsa_circ_129272 12880 RMVar_ID_12880 Human_SNP_ID_3319964 A-to-I Human chr1 + 12116689 12116689 12116689 TGGGTGTGGTGGTGGGCACCGTAGTCCCAGCTACTCAGGAGGTTGAGGCAGGAGAATCGCTTGAA TGGGTGTGGTGGTGGGCACCGTAGTCCCAGCTCCTCAGGAGGTTGAGGCAGGAGAATCGCTTGAA A C TNFRSF8 Ensembl:ENSG00000120949 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1029919268 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11038,RMVar_hsa_circ_38726,RMVar_hsa_circ_378710,RMVar_hsa_circ_88555,RMVar_hsa_circ_104848,RMVar_hsa_circ_129272,RMVar_hsa_circ_81312,RMVar_hsa_circ_129274,RMVar_hsa_circ_129276,RMVar_hsa_circ_97841,RMVar_hsa_circ_129275 12881 RMVar_ID_12881 Human_SNP_ID_3323722 A-to-I Human chr1 + 12131563 12131563 12131563 AGACAGGGTGTCACTCTGGAGTGCCATGGTACAATCATGGCTCACTGCAGCCTTGACCTCCTGGG AGACAGGGTGTCACTCTGGAGTGCCATGGTACGATCATGGCTCACTGCAGCCTTGACCTCCTGGG A G TNFRSF8 Ensembl:ENSG00000120949 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1387444865 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11038,RMVar_hsa_circ_97841,RMVar_hsa_circ_129275,RMVar_hsa_circ_118284,RMVar_hsa_circ_129278 12882 RMVar_ID_12882 Human_SNP_ID_3323742 A-to-I Human chr1 + 12131655 12131655 12131655 AGCTGGGACTACAGATACACACCACCACGCCCAGCTAACTTTTCTATTTTTTGTAGAGACCAGGT AGCTGGGACTACAGATACACACCACCACGCCCGGCTAACTTTTCTATTTTTTGTAGAGACCAGGT A G TNFRSF8 Ensembl:ENSG00000120949 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1256457282 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11038,RMVar_hsa_circ_97841,RMVar_hsa_circ_129275,RMVar_hsa_circ_118284,RMVar_hsa_circ_129278 12883 RMVar_ID_12883 Human_SNP_ID_3323764 A-to-I Human chr1 + 12131728 12131724 12131729 GTTGTGCAGGCTGGTCTCTAACTCCTGAGCTCAAGTGATCTGCCCACCTCGGCCTCCCAAAGTGC GTTGTGCAGGCTGGTCTCTAACTCCTGAG_____GTGATCTGCCCACCTCGGCCTCCCAAAGTGC GCTCAA G TNFRSF8 Ensembl:ENSG00000120949 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1246133548 Functional Loss DEL dbSNP153 30..34 33 - - - RMVar_hsa_circ_11038,RMVar_hsa_circ_97841,RMVar_hsa_circ_129275,RMVar_hsa_circ_118284,RMVar_hsa_circ_129278 12884 RMVar_ID_12884 Human_SNP_ID_3323846 A-to-I Human chr1 + 12132057 12132056 12132057 ATCGTGATTTGCCCACCTCAGCCTCCCAAAATACTGGGATTACAGGCATGAGCCACCACGCCCAG ATCGTGATTTGCCCACCTCAGCCTCCCAAAAT_CTGGGATTACAGGCATGAGCCACCACGCCCAG TA T TNFRSF8 Ensembl:ENSG00000120949 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1477393783 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_11038,RMVar_hsa_circ_97841,RMVar_hsa_circ_129275,RMVar_hsa_circ_118284,RMVar_hsa_circ_129278 12885 RMVar_ID_12885 Human_SNP_ID_3324624 A-to-I Human chr1 + 12135091 12135079 12135091 TAATCCCAGCACTTTGCAAGGCCAAGGCGGGCAGGTCAGGAGGTCAGGAGTTTGAGACCGGCCTG TAATCCCAGCACTTTGCAAGG____________GGTCAGGAGGTCAGGAGTTTGAGACCGGCCTG GCCAAGGCGGGCA G TNFRSF8 Ensembl:ENSG00000120949 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1220389418 Functional Loss DEL dbSNP153 22..33 33 - - - RMVar_hsa_circ_11038,RMVar_hsa_circ_97841,RMVar_hsa_circ_129275,RMVar_hsa_circ_118284,RMVar_hsa_circ_129278 12886 RMVar_ID_12886 Human_SNP_ID_3324670 A-to-I Human chr1 + 12135193 12135193 12135193 AAAAAATTAGCTGGGGTTGGTGGCACGAGCCTATAATCCCAGCTATTCGGGAGGCTGAGGCATGA AAAAAATTAGCTGGGGTTGGTGGCACGAGCCTGTAATCCCAGCTATTCGGGAGGCTGAGGCATGA A G TNFRSF8 Ensembl:ENSG00000120949 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1027048499 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11038,RMVar_hsa_circ_97841,RMVar_hsa_circ_129275,RMVar_hsa_circ_118284,RMVar_hsa_circ_129278 12887 RMVar_ID_12887 Human_SNP_ID_3324685 A-to-I Human chr1 + 12135255 12135255 12135255 TGAGAATCACTTGAACCCAGGAGGCGGAGGTTACATTGAGCCGAGATCATGCCACTGCACTCTAG TGAGAATCACTTGAACCCAGGAGGCGGAGGTTGCATTGAGCCGAGATCATGCCACTGCACTCTAG A G TNFRSF8 Ensembl:ENSG00000120949 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1282612452 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11038,RMVar_hsa_circ_97841,RMVar_hsa_circ_129275,RMVar_hsa_circ_118284,RMVar_hsa_circ_129278 12888 RMVar_ID_12888 Human_SNP_ID_3340503 A-to-I Human chr1 + 12196072 12196072 12196072 CCTGTAATCCCAGCACTTTGGAAGGCCGAGGTAGATGGATCACTTGAGGTCAGGAGTTCAAGACT CCTGTAATCCCAGCACTTTGGAAGGCCGAGGTGGATGGATCACTTGAGGTCAGGAGTTCAAGACT A G TNFRSF1B Ensembl:ENSG00000028137 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs542020588 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99634,RMVar_hsa_circ_129280,RMVar_hsa_circ_268591,RMVar_hsa_circ_89585,RMVar_hsa_circ_129281 12889 RMVar_ID_12889 Human_SNP_ID_3340754 A-to-I Human chr1 + 12197087 12197087 12197087 ATCCCACCTCAGCCTCCCAAGTAGATGGGACTATGGGCATGCGCCACCATGCCTGGCTAATTTTT ATCCCACCTCAGCCTCCCAAGTAGATGGGACTGTGGGCATGCGCCACCATGCCTGGCTAATTTTT A G TNFRSF1B Ensembl:ENSG00000028137 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs550337080 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99634,RMVar_hsa_circ_129280,RMVar_hsa_circ_268591,RMVar_hsa_circ_89585,RMVar_hsa_circ_129281 12890 RMVar_ID_12890 Human_SNP_ID_3340755 A-to-I Human chr1 + 12197087 12197087 12197087 ATCCCACCTCAGCCTCCCAAGTAGATGGGACTATGGGCATGCGCCACCATGCCTGGCTAATTTTT ATCCCACCTCAGCCTCCCAAGTAGATGGGACTTTGGGCATGCGCCACCATGCCTGGCTAATTTTT A T TNFRSF1B Ensembl:ENSG00000028137 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs550337080 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99634,RMVar_hsa_circ_129280,RMVar_hsa_circ_268591,RMVar_hsa_circ_89585,RMVar_hsa_circ_129281 12891 RMVar_ID_12891 Human_SNP_ID_3340762 A-to-I Human chr1 + 12197120 12197120 12197120 TGGGCATGCGCCACCATGCCTGGCTAATTTTTATATTTTTAGTAGAGACGGGGTTTTGCCATGTT TGGGCATGCGCCACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTTGCCATGTT A G TNFRSF1B Ensembl:ENSG00000028137 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs539244291 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99634,RMVar_hsa_circ_129280,RMVar_hsa_circ_268591,RMVar_hsa_circ_89585,RMVar_hsa_circ_129281 12892 RMVar_ID_12892 Human_SNP_ID_3341782 A-to-I Human chr1 + 12201071 12201071 12201071 GCCCAGGAGTACAAGACCAGCCTGGGTAACATAGCACAACCCTGTCTCTACAAACAATCGACAAC GCCCAGGAGTACAAGACCAGCCTGGGTAACATGGCACAACCCTGTCTCTACAAACAATCGACAAC A G TNFRSF1B Ensembl:ENSG00000028137 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs964378416 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99634,RMVar_hsa_circ_129280,RMVar_hsa_circ_268591,RMVar_hsa_circ_89585,RMVar_hsa_circ_129281 12893 RMVar_ID_12893 Human_SNP_ID_3398390 A-to-I Human chr1 + 12432138 12432138 12432138 AGAGCAAGCCAGGTGCGGTGGCTTACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGCGG AGAGCAAGCCAGGTGCGGTGGCTTACACCTGTGATCCCAGCACTTTGGGAGGCTGAGGCGGGCGG A G VPS13D Ensembl:ENSG00000048707 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1368560296 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9335,RMVar_hsa_circ_25973,RMVar_hsa_circ_2696,RMVar_hsa_circ_61623,RMVar_hsa_circ_337024,RMVar_hsa_circ_288417,RMVar_hsa_circ_68558,RMVar_hsa_circ_337564,RMVar_hsa_circ_336857,RMVar_hsa_circ_13712,RMVar_hsa_circ_23802,RMVar_hsa_circ_352358 12894 RMVar_ID_12894 Human_SNP_ID_3706071 A-to-I Human chr1 + 13654159 13654159 13654159 GAGGCAGGAGGATCACTTGAGCCCAGTAGTTCAAGACCAGCCTGGGCAATATAGTGAGACCTCAT GAGGCAGGAGGATCACTTGAGCCCAGTAGTTCGAGACCAGCCTGGGCAATATAGTGAGACCTCAT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1447477291 Functional Loss SNV dbSNP153 33..33 33 - - - 12895 RMVar_ID_12895 Human_SNP_ID_3729427 A-to-I Human chr1 - 13750521 13750521 13750521 ATTTTAACATTTTCCCAAATCGAGTTTACGATATGATTTTATTTACAGTATGACTTCCACAACTC ATTTTAACATTTTCCCAAATCGAGTTTACGATGTGATTTTATTTACAGTATGACTTCCACAACTC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1169673054 Functional Loss SNV dbSNP153 33..33 33 - - - 12896 RMVar_ID_12896 Human_SNP_ID_3974960 A-to-I Human chr1 + 14727700 14727700 14727700 GTTGGTCAGGCTGGTCTCGAACTCCCGACCTGAGGTAATCCGCCCACCACGGCCTCCCTAAGTGT GTTGGTCAGGCTGGTCTCGAACTCCCGACCTGGGGTAATCCGCCCACCACGGCCTCCCTAAGTGT A G KAZN Ensembl:ENSG00000189337 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1323035050 Functional Loss SNV dbSNP153 33..33 33 - - - 12897 RMVar_ID_12897 Human_SNP_ID_3998134 A-to-I Human chr1 + 14821386 14821385 14821386 AAATACAAAACAAATTAGCCAGGTGTTGTGGCAGGCACCTGTAATCCCAGCTACTTGGGAGGCTG AAATACAAAACAAATTAGCCAGGTGTTGTGGC_GGCACCTGTAATCCCAGCTACTTGGGAGGCTG CA C KAZN Ensembl:ENSG00000189337 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs754970377 Functional Loss DEL dbSNP153 33..33 33 - - - 12898 RMVar_ID_12898 Human_SNP_ID_3998144 A-to-I Human chr1 + 14821442 14821442 14821442 GGGAGGCTGAGGCAGGAGAATCGCTTGAACCCAGGAGGTGGAGGTTGCAGTGAGTGGAGATAGCT GGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGGGAGGTGGAGGTTGCAGTGAGTGGAGATAGCT A G KAZN Ensembl:ENSG00000189337 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs200857438 Functional Loss SNV dbSNP153 33..33 33 - - - 12899 RMVar_ID_12899 Human_SNP_ID_681176779 A-to-I Human chr20 + 41029087 41029087 41029087 CCTCCGGGCCGACATGAGTGGGGACCACCTCCACAACGATTCCCAGGTACGGCCCGGCCTGACCC CCTCCGGGCCGACATGAGTGGGGACCACCTCCGCAACGATTCCCAGGTACGGCCCGGCCTGACCC A G TOP1 Ensembl:ENSG00000198900 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs771124146 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_925772,Human_RBP_ID_1026082,Human_RBP_ID_8533486,Human_RBP_ID_19108410,Human_RBP_ID_23258181 Human_Splice_Rec_2083671 12900 RMVar_ID_12900 Human_SNP_ID_681179363 A-to-I Human chr20 + 41039667 41039667 41039667 GTAATGGCTCATGCCTGTAATTCCACCATTTTAGGAGGCCGAGGCGGGCGGATCACGAGGTCAGG GTAATGGCTCATGCCTGTAATTCCACCATTTTCGGAGGCCGAGGCGGGCGGATCACGAGGTCAGG A C TOP1 Ensembl:ENSG00000198900 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1294846788 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_150532,Human_RBP_ID_24380122 12901 RMVar_ID_12901 Human_SNP_ID_681179391 A-to-I Human chr20 + 41039753 41039752 41039753 ACACGGCGAAACCCCGTCTCTACTAAAAATACAAAAAACTAGCCGGGCGTGGTGGCGGGCGCCTG ACACGGCGAAACCCCGTCTCTACTAAAAATAC_AAAAACTAGCCGGGCGTGGTGGCGGGCGCCTG CA C TOP1 Ensembl:ENSG00000198900 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1341880084 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_150532 12902 RMVar_ID_12902 Human_SNP_ID_681180008 A-to-I Human chr20 + 41042054 41042054 41042054 CCTCATCCTCCTGAGTACCTGGGATTACAGGCACACCACCACCACACCTGGCTAATTTTTGTATT CCTCATCCTCCTGAGTACCTGGGATTACAGGCGCACCACCACCACACCTGGCTAATTTTTGTATT A G TOP1 Ensembl:ENSG00000198900 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs963772964 Functional Loss SNV dbSNP153 33..33 33 - - - 12903 RMVar_ID_12903 Human_SNP_ID_681183286 A-to-I Human chr20 + 41056581 41056581 41056581 AATCATAGCTCCATCCTTGAACTCCTGTGCCCAAGCAGTCTTCCCACCTCACCCTCAGAGCAGCC AATCATAGCTCCATCCTTGAACTCCTGTGCCCCAGCAGTCTTCCCACCTCACCCTCAGAGCAGCC A C TOP1 Ensembl:ENSG00000198900 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1475083691 Functional Loss SNV dbSNP153 33..33 33 - - - 12904 RMVar_ID_12904 Human_SNP_ID_681194075 A-to-I Human chr20 + 41103530 41103530 41103530 TATGTAAATCACATCAGTAAATATGAACTGTTATAAATGCTGCAAAGGAAAAAGTACAGGGTGCC TATGTAAATCACATCAGTAAATATGAACTGTTTTAAATGCTGCAAAGGAAAAAGTACAGGGTGCC A T TOP1 Ensembl:ENSG00000198900 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1282730088 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9005,RMVar_hsa_circ_78804,RMVar_hsa_circ_210163,RMVar_hsa_circ_22116,RMVar_hsa_circ_352483,RMVar_hsa_circ_377431,RMVar_hsa_circ_291682,RMVar_hsa_circ_13744 12905 RMVar_ID_12905 Human_SNP_ID_681198026 A-to-I Human chr20 + 41120993 41120993 41120993 TTGATCTCCTGACCTTGTGATCCGCCCTCCTCAGCCTCCCCAAAGTGCTGGGATTACAGGCGTGA TTGATCTCCTGACCTTGTGATCCGCCCTCCTCGGCCTCCCCAAAGTGCTGGGATTACAGGCGTGA A G TOP1 Ensembl:ENSG00000198900 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1241075376 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42037 12906 RMVar_ID_12906 Human_SNP_ID_681200191 A-to-I Human chr20 - 41130261 41130261 41130261 ATATAAAAATAAAAAAATTAGCCAGGCATGGTAGCATGCACCTGTAGTCTCAGCTCTTCAGGAAG ATATAAAAATAAAAAAATTAGCCAGGCATGGTGGCATGCACCTGTAGTCTCAGCTCTTCAGGAAG T C PLCG1-AS1 Ensembl:ENSG00000226648 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1489203296 Functional Loss SNV dbSNP153 33..33 33 - - - 12907 RMVar_ID_12907 Human_SNP_ID_681276838 A-to-I Human chr20 - 41435399 41435399 41435399 TGTAGAGACAGGGTCTTGCTGTTGCCCAGGCTAGTATTGAACTCCTGAGTTCAAGCAATCCTCCC TGTAGAGACAGGGTCTTGCTGTTGCCCAGGCTGGTATTGAACTCCTGAGTTCAAGCAATCCTCCC T C CHD6 Ensembl:ENSG00000124177 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1291255226 Functional Loss SNV dbSNP153 33..33 33 - - - 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_210204,RMVar_hsa_circ_210205 12908 RMVar_ID_12908 Human_SNP_ID_681285723 A-to-I Human chr20 - 41472051 41472051 41472051 TTTTGTATTTTTAGTAAAGATGGGATTTTGCTATGTTGGGCATGCCGGTCTTGAACTCCTGACCT TTTTGTATTTTTAGTAAAGATGGGATTTTGCTGTGTTGGGCATGCCGGTCTTGAACTCCTGACCT T C CHD6 Ensembl:ENSG00000124177 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs970278115 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70084,RMVar_hsa_circ_84895,RMVar_hsa_circ_210205,RMVar_hsa_circ_68449,RMVar_hsa_circ_11813,RMVar_hsa_circ_118701,RMVar_hsa_circ_47944,RMVar_hsa_circ_210208,RMVar_hsa_circ_210209 12909 RMVar_ID_12909 Human_SNP_ID_681285724 A-to-I Human chr20 - 41472051 41472051 41472051 TTTTGTATTTTTAGTAAAGATGGGATTTTGCTATGTTGGGCATGCCGGTCTTGAACTCCTGACCT TTTTGTATTTTTAGTAAAGATGGGATTTTGCTCTGTTGGGCATGCCGGTCTTGAACTCCTGACCT T G CHD6 Ensembl:ENSG00000124177 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs970278115 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70084,RMVar_hsa_circ_84895,RMVar_hsa_circ_210205,RMVar_hsa_circ_68449,RMVar_hsa_circ_11813,RMVar_hsa_circ_118701,RMVar_hsa_circ_47944,RMVar_hsa_circ_210208,RMVar_hsa_circ_210209 12910 RMVar_ID_12910 Human_SNP_ID_681318094 A-to-I Human chr20 - 41602871 41602871 41602871 CGAGACCAGCCTGGTCAGCATATTGAGACCCTATCTCTACAAAATATTTTAAAAATTAGCCCGGT CGAGACCAGCCTGGTCAGCATATTGAGACCCTGTCTCTACAAAATATTTTAAAAATTAGCCCGGT T C CHD6 Ensembl:ENSG00000124177 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1172876554 Functional Loss SNV dbSNP153 33..33 33 - - - 12911 RMVar_ID_12911 Human_SNP_ID_681318095 A-to-I Human chr20 - 41602871 41602871 41602871 CGAGACCAGCCTGGTCAGCATATTGAGACCCTATCTCTACAAAATATTTTAAAAATTAGCCCGGT CGAGACCAGCCTGGTCAGCATATTGAGACCCTCTCTCTACAAAATATTTTAAAAATTAGCCCGGT T G CHD6 Ensembl:ENSG00000124177 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1172876554 Functional Loss SNV dbSNP153 33..33 33 - - - 12912 RMVar_ID_12912 Human_SNP_ID_681719338 A-to-I Human chr20 + 43201477 43201477 43201477 TTACGGGTTTTAGGTTTTGTTTTCCTCCTGACAGCTCCTGGACTTTTTAAAATTCCTGTAATTGT TTACGGGTTTTAGGTTTTGTTTTCCTCCTGACGGCTCCTGGACTTTTTAAAATTCCTGTAATTGT A G AL021395.1 Ensembl:ENSG00000233508 lincRNA exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs548367154 Functional Loss SNV dbSNP153 33..33 33 - - - 12913 RMVar_ID_12913 Human_SNP_ID_681786835 A-to-I Human chr20 + 43467395 43467395 43467395 CCATCTGCTCAGGAGGCTGAGGTGGGAGGATCACTTGAGCCCAGGAGGTTAAGGCTGCATTGAGC CCATCTGCTCAGGAGGCTGAGGTGGGAGGATCGCTTGAGCCCAGGAGGTTAAGGCTGCATTGAGC A G AL031681.3 Ensembl:ENSG00000288000 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1389319135 Functional Loss SNV dbSNP153 33..33 33 - - - 12914 RMVar_ID_12914 Human_SNP_ID_681787407 A-to-I Human chr20 + 43469231 43469228 43469232 TTTTCTTTTTTGAGTTAGGGTCTCACTCTGTTACTTAGGCTGGAATACAGTGGCATGATCACGGC TTTTCTTTTTTGAGTTAGGGTCTCACTCTG____TTAGGCTGGAATACAGTGGCATGATCACGGC GTTAC G AL031681.3 Ensembl:ENSG00000288000 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1352584224 Functional Loss DEL dbSNP153 31..34 33 - - - 12915 RMVar_ID_12915 Human_SNP_ID_681800385 A-to-I Human chr20 + 43519753 43519753 43519753 GCCTCAAACTCCTGGGCTCAAGGGATCCTTCTACTTAAGCCTTCTGAGTAACTGGGACTACAGGC GCCTCAAACTCCTGGGCTCAAGGGATCCTTCTGCTTAAGCCTTCTGAGTAACTGGGACTACAGGC A G AL031681.3,L3MBTL1 Ensembl:ENSG00000288000,Ensembl:ENSG00000185513 Protein coding,Protein coding intron,intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1458068380 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1016,RMVar_hsa_circ_111125,RMVar_hsa_circ_93574,RMVar_hsa_circ_210246,RMVar_hsa_circ_87499,RMVar_hsa_circ_210247,RMVar_hsa_circ_210248 12916 RMVar_ID_12916 Human_SNP_ID_681800827 A-to-I Human chr20 + 43521742 43521742 43521742 TTATTTTATTTTTTATCATTATTTTTAGAGACAGGGTCTTACTGTGTTGCCCAGACTGGCCTTAA TTATTTTATTTTTTATCATTATTTTTAGAGACGGGGTCTTACTGTGTTGCCCAGACTGGCCTTAA A G AL031681.3,L3MBTL1 Ensembl:ENSG00000288000,Ensembl:ENSG00000185513 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs73105340 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1016,RMVar_hsa_circ_111125,RMVar_hsa_circ_93574,RMVar_hsa_circ_210246,RMVar_hsa_circ_87499,RMVar_hsa_circ_210247,RMVar_hsa_circ_210248 12917 RMVar_ID_12917 Human_SNP_ID_681800831 A-to-I Human chr20 + 43521787 43521787 43521787 GTTGCCCAGACTGGCCTTAAACTCCTGAGTGCAAGCGATCCTCCTGCCTCAGCCTTCTGAGTAGC GTTGCCCAGACTGGCCTTAAACTCCTGAGTGCGAGCGATCCTCCTGCCTCAGCCTTCTGAGTAGC A G AL031681.3,L3MBTL1 Ensembl:ENSG00000288000,Ensembl:ENSG00000185513 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1471256459 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23311450 RMVar_hsa_circ_1016,RMVar_hsa_circ_111125,RMVar_hsa_circ_93574,RMVar_hsa_circ_210246,RMVar_hsa_circ_87499,RMVar_hsa_circ_210247,RMVar_hsa_circ_210248 12918 RMVar_ID_12918 Human_SNP_ID_681801206 A-to-I Human chr20 + 43522845 43522845 43522845 TGTCAGATGGCCGGGCATGGTAGCTCACCTCTATAATCCCAGCACTTTAGTAGGCCAAGGCAGGT TGTCAGATGGCCGGGCATGGTAGCTCACCTCTGTAATCCCAGCACTTTAGTAGGCCAAGGCAGGT A G AL031681.3,L3MBTL1 Ensembl:ENSG00000288000,Ensembl:ENSG00000185513 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1160774146 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1016,RMVar_hsa_circ_111125,RMVar_hsa_circ_93574,RMVar_hsa_circ_210246,RMVar_hsa_circ_87499,RMVar_hsa_circ_210247,RMVar_hsa_circ_210248 12919 RMVar_ID_12919 Human_SNP_ID_681838899 A-to-I Human chr20 + 43669045 43669045 43669045 GCCGCCACGCCTGGCTAATTTTTTGGATTTTTAGTAGAGATGGGTTTCACTGTGTTGCTCAGGCA GCCGCCACGCCTGGCTAATTTTTTGGATTTTTGGTAGAGATGGGTTTCACTGTGTTGCTCAGGCA A G MYBL2 Ensembl:ENSG00000101057 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs747579169 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14114299,Human_RBP_ID_25613580 RMVar_hsa_circ_96108,RMVar_hsa_circ_118554,RMVar_hsa_circ_210269,RMVar_hsa_circ_210270 12920 RMVar_ID_12920 Human_SNP_ID_681839131 A-to-I Human chr20 + 43670025 43670025 43670025 ATTCGGGAGGCTGAGGCAGGAGAATTCACTTGAACCCAGGAGGCAGAGGTTGCTGTGAGTCGAGA ATTCGGGAGGCTGAGGCAGGAGAATTCACTTGTACCCAGGAGGCAGAGGTTGCTGTGAGTCGAGA A T MYBL2 Ensembl:ENSG00000101057 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1267938229 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14114347 RMVar_hsa_circ_96108,RMVar_hsa_circ_118554,RMVar_hsa_circ_210269,RMVar_hsa_circ_210270 12921 RMVar_ID_12921 Human_SNP_ID_681839760 A-to-I Human chr20 + 43672200 43672200 43672200 GCCACTTCACTCTAGCCTGGGTGACAGAGTGAAACTCCGTCTCAAAAAAAAAAAATAGATACTGT GCCACTTCACTCTAGCCTGGGTGACAGAGTGAGACTCCGTCTCAAAAAAAAAAAATAGATACTGT A G MYBL2 Ensembl:ENSG00000101057 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs532250652 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14114411 RMVar_hsa_circ_96108,RMVar_hsa_circ_118554,RMVar_hsa_circ_210269,RMVar_hsa_circ_210270 12922 RMVar_ID_12922 Human_SNP_ID_681840013 A-to-I Human chr20 + 43673118 43673118 43673118 GGCATGCGCCACCGCACCCAGCTAATATTTGTATTTTTAGTAGAGATGGGGTTTCACTGTGTTTG GGCATGCGCCACCGCACCCAGCTAATATTTGTGTTTTTAGTAGAGATGGGGTTTCACTGTGTTTG A G MYBL2 Ensembl:ENSG00000101057 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1189277258 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96108,RMVar_hsa_circ_118554,RMVar_hsa_circ_210269,RMVar_hsa_circ_210270 12923 RMVar_ID_12923 Human_SNP_ID_681840112 A-to-I Human chr20 + 43673530 43673530 43673530 GTGGTGGCATACCCCTGTAGTCACAGCTACTTAGGAGGCTGGGGCGGGACGATCATTTGAGTCCA GTGGTGGCATACCCCTGTAGTCACAGCTACTTGGGAGGCTGGGGCGGGACGATCATTTGAGTCCA A G MYBL2 Ensembl:ENSG00000101057 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs113903244 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96108,RMVar_hsa_circ_118554,RMVar_hsa_circ_210269,RMVar_hsa_circ_210270 12924 RMVar_ID_12924 Human_SNP_ID_681840246 A-to-I Human chr20 + 43673883 43673883 43673883 GCCGGAGCAGAGGGATAGCAAGTGCAAGGTCAAATGGACCCATGAGGAGGTGAGTGCCATGGGGA GCCGGAGCAGAGGGATAGCAAGTGCAAGGTCAGATGGACCCATGAGGAGGTGAGTGCCATGGGGA A G MYBL2 Ensembl:ENSG00000101057 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1488312264 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_925883,Human_RBP_ID_1026163,Human_RBP_ID_4659851,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 12925 RMVar_ID_12925 Human_SNP_ID_681842167 A-to-I Human chr20 + 43680308 43680308 43680308 CCTCGGCCTCCTGAAGTGTTGGGGTTAAAGGCATGAGCCACTGCTCCCTGCCTGATTTTGACTAT CCTCGGCCTCCTGAAGTGTTGGGGTTAAAGGCGTGAGCCACTGCTCCCTGCCTGATTTTGACTAT A G MYBL2 Ensembl:ENSG00000101057 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs427015 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_1000,GWAS_ID_1001,GWAS_ID_1002,GWAS_ID_1003,GWAS_ID_1004,GWAS_ID_1005,GWAS_ID_1006,GWAS_ID_1007,GWAS_ID_1008,GWAS_ID_1009,GWAS_ID_1010,GWAS_ID_1011,GWAS_ID_1012,GWAS_ID_1013,GWAS_ID_1014,GWAS_ID_1015,GWAS_ID_1016,GWAS_ID_1017,GWAS_ID_1018,GWAS_ID_1019,GWAS_ID_1020,GWAS_ID_1021,GWAS_ID_1022,GWAS_ID_1023,GWAS_ID_1024,GWAS_ID_1025,GWAS_ID_1026,GWAS_ID_1027,GWAS_ID_1028 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 12926 RMVar_ID_12926 Human_SNP_ID_681842444 A-to-I Human chr20 + 43681378 43681378 43681378 TCTTCAAACACATCAGTGGTTTTGCATGATAGATGGTTGAACTGATGCTGCGAATGGTCTGGCCC TCTTCAAACACATCAGTGGTTTTGCATGATAGGTGGTTGAACTGATGCTGCGAATGGTCTGGCCC A G MYBL2 Ensembl:ENSG00000101057 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs433732 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_1029,GWAS_ID_1030,GWAS_ID_1031,GWAS_ID_1032,GWAS_ID_1033,GWAS_ID_1034,GWAS_ID_1035,GWAS_ID_1036,GWAS_ID_1037,GWAS_ID_1038,GWAS_ID_1039,GWAS_ID_1040,GWAS_ID_1041,GWAS_ID_1042,GWAS_ID_1043,GWAS_ID_1044,GWAS_ID_1045,GWAS_ID_1046,GWAS_ID_1047,GWAS_ID_1048,GWAS_ID_1049,GWAS_ID_1050,GWAS_ID_1051,GWAS_ID_1052,GWAS_ID_1053,GWAS_ID_1054,GWAS_ID_1055,GWAS_ID_1056,GWAS_ID_1057,GWAS_ID_1058,GWAS_ID_1059,GWAS_ID_1060,GWAS_ID_1061,GWAS_ID_1062,GWAS_ID_1063,GWAS_ID_1064,GWAS_ID_1065,GWAS_ID_1066,GWAS_ID_1067,GWAS_ID_1068,GWAS_ID_1069,GWAS_ID_1070,GWAS_ID_1071,GWAS_ID_1072,GWAS_ID_1073,GWAS_ID_1074,GWAS_ID_1075,GWAS_ID_1076,GWAS_ID_1077,GWAS_ID_1078,GWAS_ID_1079,GWAS_ID_1080,GWAS_ID_1081,GWAS_ID_1082,GWAS_ID_1083,GWAS_ID_1084,GWAS_ID_1085,GWAS_ID_1086,GWAS_ID_1087,GWAS_ID_1088,GWAS_ID_1089,GWAS_ID_1090,GWAS_ID_1091,GWAS_ID_1092,GWAS_ID_1093,GWAS_ID_1094,GWAS_ID_1095,GWAS_ID_1096,GWAS_ID_1097,GWAS_ID_1098,GWAS_ID_1099,GWAS_ID_1100,GWAS_ID_1101,GWAS_ID_1102,GWAS_ID_1103,GWAS_ID_1104,GWAS_ID_1105,GWAS_ID_1106,GWAS_ID_1107,GWAS_ID_1108,GWAS_ID_1109 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 12927 RMVar_ID_12927 Human_SNP_ID_681843109 A-to-I Human chr20 + 43683623 43683623 43683623 TCGCTCAGGTTAGAGTGCAGTGGCGCGATCTCAGCTCACTGCATCCTCCGCCTCCCGGGTTCAAG TCGCTCAGGTTAGAGTGCAGTGGCGCGATCTCGGCTCACTGCATCCTCCGCCTCCCGGGTTCAAG A G MYBL2 Ensembl:ENSG00000101057 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs372134147 Functional Loss SNV dbSNP153 33..33 33 - - - 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_96263,RMVar_hsa_circ_306682,RMVar_hsa_circ_210273,RMVar_hsa_circ_92101,RMVar_hsa_circ_375181,RMVar_hsa_circ_53095,RMVar_hsa_circ_210276,RMVar_hsa_circ_210274,RMVar_hsa_circ_210275,RMVar_hsa_circ_126773 12928 RMVar_ID_12928 Human_SNP_ID_681843521 A-to-I Human chr20 + 43685088 43685088 43685088 AGAATCACCTGAAGTGGGGAGGCGGAGGTTGCAGTGAGCCGAGATGGCGCCATTGTACTCCAGCC AGAATCACCTGAAGTGGGGAGGCGGAGGTTGCGGTGAGCCGAGATGGCGCCATTGTACTCCAGCC A G MYBL2 Ensembl:ENSG00000101057 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1555810797 Functional Loss SNV dbSNP153 33..33 33 - - - 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_96263,RMVar_hsa_circ_306682,RMVar_hsa_circ_210273,RMVar_hsa_circ_92101,RMVar_hsa_circ_375181,RMVar_hsa_circ_53095,RMVar_hsa_circ_210276,RMVar_hsa_circ_210274,RMVar_hsa_circ_210275,RMVar_hsa_circ_126773 12929 RMVar_ID_12929 Human_SNP_ID_681843522 A-to-I Human chr20 + 43685092 43685092 43685092 TCACCTGAAGTGGGGAGGCGGAGGTTGCAGTGAGCCGAGATGGCGCCATTGTACTCCAGCCTGGG TCACCTGAAGTGGGGAGGCGGAGGTTGCAGTGCGCCGAGATGGCGCCATTGTACTCCAGCCTGGG A C MYBL2 Ensembl:ENSG00000101057 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444218405 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14114722 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_96263,RMVar_hsa_circ_306682,RMVar_hsa_circ_210273,RMVar_hsa_circ_92101,RMVar_hsa_circ_375181,RMVar_hsa_circ_53095,RMVar_hsa_circ_210276,RMVar_hsa_circ_210274,RMVar_hsa_circ_210275,RMVar_hsa_circ_126773 12930 RMVar_ID_12930 Human_SNP_ID_681843527 A-to-I Human chr20 + 43685099 43685099 43685099 AAGTGGGGAGGCGGAGGTTGCAGTGAGCCGAGATGGCGCCATTGTACTCCAGCCTGGGCAGCAGG AAGTGGGGAGGCGGAGGTTGCAGTGAGCCGAGGTGGCGCCATTGTACTCCAGCCTGGGCAGCAGG A G MYBL2 Ensembl:ENSG00000101057 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs553712143 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14114722 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_96263,RMVar_hsa_circ_306682,RMVar_hsa_circ_210273,RMVar_hsa_circ_92101,RMVar_hsa_circ_375181,RMVar_hsa_circ_53095,RMVar_hsa_circ_210276,RMVar_hsa_circ_210274,RMVar_hsa_circ_210275,RMVar_hsa_circ_126773 12931 RMVar_ID_12931 Human_SNP_ID_681844476 A-to-I Human chr20 + 43688423 43688423 43688423 GGAATTTCACCATGTTGGCCAGGCTGGTCTCGAACTCTTGACCTCCTGCCCACCTCAGCCTCACA GGAATTTCACCATGTTGGCCAGGCTGGTCTCGTACTCTTGACCTCCTGCCCACCTCAGCCTCACA A T MYBL2 Ensembl:ENSG00000101057 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1000333765 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96108,RMVar_hsa_circ_118554,RMVar_hsa_circ_346978,RMVar_hsa_circ_210269,RMVar_hsa_circ_210270,RMVar_hsa_circ_96263,RMVar_hsa_circ_210273,RMVar_hsa_circ_92101,RMVar_hsa_circ_375181,RMVar_hsa_circ_53095,RMVar_hsa_circ_92301,RMVar_hsa_circ_210276,RMVar_hsa_circ_210274,RMVar_hsa_circ_210275,RMVar_hsa_circ_126773,RMVar_hsa_circ_297485,RMVar_hsa_circ_348575,RMVar_hsa_circ_313329,RMVar_hsa_circ_284606,RMVar_hsa_circ_210278,RMVar_hsa_circ_210280,RMVar_hsa_circ_76011,RMVar_hsa_circ_210279,RMVar_hsa_circ_210277 12932 RMVar_ID_12932 Human_SNP_ID_681997764 A-to-I Human chr20 - 44306094 44306094 44306094 CTGAGATTGGGAGTTCGAGACCAGCCTGTCCAACATGGCGAACCTCGTCTCTTCTAAAAATACAA CTGAGATTGGGAGTTCGAGACCAGCCTGTCCAGCATGGCGAACCTCGTCTCTTCTAAAAATACAA T C FITM2 Ensembl:ENSG00000197296 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs530080918 Functional Loss SNV dbSNP153 33..33 33 - - - 12933 RMVar_ID_12933 Human_SNP_ID_681997767 A-to-I Human chr20 - 44306104 44306104 44306104 GGCGGATCACCTGAGATTGGGAGTTCGAGACCAGCCTGTCCAACATGGCGAACCTCGTCTCTTCT GGCGGATCACCTGAGATTGGGAGTTCGAGACCGGCCTGTCCAACATGGCGAACCTCGTCTCTTCT T C FITM2 Ensembl:ENSG00000197296 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs892227990 Functional Loss SNV dbSNP153 33..33 33 - - - 12934 RMVar_ID_12934 Human_SNP_ID_681999050 A-to-I Human chr20 - 44311109 44311109 44311109 ATCTGGAGCGCTGCGAGTGGTTGTTGCGGGGGACGCTGGTGCGGGCGGCCGTGCGGCGCTACCTG ATCTGGAGCGCTGCGAGTGGTTGTTGCGGGGGTCGCTGGTGCGGGCGGCCGTGCGGCGCTACCTG T A FITM2 Ensembl:ENSG00000197296 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1449584842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4659410,Human_RBP_ID_5148430,Human_RBP_ID_22453100 12935 RMVar_ID_12935 Human_SNP_ID_682041020 A-to-I Human chr20 + 44477996 44477996 44477996 ATTTAAAAATTAGCCAGGCGTGGTGTGTGCCTATAGTCCCAGCTACCTGGGAGGCTGAGGCAGGA ATTTAAAAATTAGCCAGGCGTGGTGTGTGCCTGTAGTCCCAGCTACCTGGGAGGCTGAGGCAGGA A G TTPAL Ensembl:ENSG00000124120 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs60633135 Functional Loss SNV dbSNP153 33..33 33 - - - 12936 RMVar_ID_12936 Human_SNP_ID_682046525 A-to-I Human chr20 - 44500259 44500259 44500259 CTGAGTGCCAAGGACACCACTGGAACTCACAAAGGTCTCCTTCACCGAAAACCCATATACCTTTT CTGAGTGCCAAGGACACCACTGGAACTCACAAGGGTCTCCTTCACCGAAAACCCATATACCTTTT T C SERINC3 Ensembl:ENSG00000132824 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1057016339 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_927169,Human_RBP_ID_1597719,Human_RBP_ID_1930270,Human_RBP_ID_8534074,Human_RBP_ID_17281611,Human_RBP_ID_17395566,Human_RBP_ID_17511759,Human_RBP_ID_18773786,Human_RBP_ID_22395182,Human_RBP_ID_22452781,Human_RBP_ID_27486140 Human_Splice_Rec_2086775,Human_Splice_Rec_2086795 Human_miRNA_ID_2622064,Human_miRNA_ID_2622065,Human_miRNA_ID_3080111,Human_miRNA_ID_3080112 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 12937 RMVar_ID_12937 Human_SNP_ID_682047109 A-to-I Human chr20 - 44502575 44502573 44502576 GTGTTTTTTTTTTTTTTTTTTTGAAGAGAAGAAGTGTTGCTCTGTCATCCAGGCTGGAATGCAGT GTGTTTTTTTTTTTTTTTTTTTGAAGAGAAG___TGTTGCTCTGTCATCCAGGCTGGAATGCAGT ACTT A SERINC3 Ensembl:ENSG00000132824 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1391891699 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_79966,RMVar_hsa_circ_96393,RMVar_hsa_circ_210310,RMVar_hsa_circ_41038,RMVar_hsa_circ_29706,RMVar_hsa_circ_362777,RMVar_hsa_circ_210311,RMVar_hsa_circ_210312 12938 RMVar_ID_12938 Human_SNP_ID_682047110 A-to-I Human chr20 - 44502575 44502575 44502575 GTGTTTTTTTTTTTTTTTTTTTGAAGAGAAGAAGTGTTGCTCTGTCATCCAGGCTGGAATGCAGT GTGTTTTTTTTTTTTTTTTTTTGAAGAGAAGAGGTGTTGCTCTGTCATCCAGGCTGGAATGCAGT T C SERINC3 Ensembl:ENSG00000132824 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1189027860 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79966,RMVar_hsa_circ_96393,RMVar_hsa_circ_210310,RMVar_hsa_circ_41038,RMVar_hsa_circ_29706,RMVar_hsa_circ_362777,RMVar_hsa_circ_210311,RMVar_hsa_circ_210312 12939 RMVar_ID_12939 Human_SNP_ID_682047916 A-to-I Human chr20 - 44505563 44505563 44505563 TAATCCCAGCACTTTGGGAGGCCAAGGCGGGCAGATCACCTGAGGTCAGGAGTTCAAGACCAGCT TAATCCCAGCACTTTGGGAGGCCAAGGCGGGCGGATCACCTGAGGTCAGGAGTTCAAGACCAGCT T C SERINC3 Ensembl:ENSG00000132824 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1453168498 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3803,RMVar_hsa_circ_96393,RMVar_hsa_circ_210310,RMVar_hsa_circ_41038,RMVar_hsa_circ_29706,RMVar_hsa_circ_362777,RMVar_hsa_circ_210312,RMVar_hsa_circ_299348,RMVar_hsa_circ_324780,RMVar_hsa_circ_358561,RMVar_hsa_circ_318234,RMVar_hsa_circ_294719,RMVar_hsa_circ_210314,RMVar_hsa_circ_210316,RMVar_hsa_circ_210315,RMVar_hsa_circ_210313,RMVar_hsa_circ_11228 12940 RMVar_ID_12940 Human_SNP_ID_682047933 A-to-I Human chr20 - 44505609 44505609 44505609 GGGCAATAAGAGCGAAACTCCAGCTTGGCGTGATGGCTCATGCCTGTAATCCCAGCACTTTGGGA GGGCAATAAGAGCGAAACTCCAGCTTGGCGTGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGA T C SERINC3 Ensembl:ENSG00000132824 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1368837571 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3803,RMVar_hsa_circ_96393,RMVar_hsa_circ_210310,RMVar_hsa_circ_41038,RMVar_hsa_circ_29706,RMVar_hsa_circ_362777,RMVar_hsa_circ_210312,RMVar_hsa_circ_299348,RMVar_hsa_circ_324780,RMVar_hsa_circ_358561,RMVar_hsa_circ_318234,RMVar_hsa_circ_294719,RMVar_hsa_circ_210314,RMVar_hsa_circ_210316,RMVar_hsa_circ_210315,RMVar_hsa_circ_210313,RMVar_hsa_circ_11228 12941 RMVar_ID_12941 Human_SNP_ID_682048052 A-to-I Human chr20 - 44506044 44506044 44506044 CACCCATCTCAGCCTCCCAAAGTGCTGGTTTTACAGTTGTGAGCCACCGCATGTGGCTGGGAATG CACCCATCTCAGCCTCCCAAAGTGCTGGTTTTGCAGTTGTGAGCCACCGCATGTGGCTGGGAATG T C SERINC3 Ensembl:ENSG00000132824 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs963526312 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3803,RMVar_hsa_circ_96393,RMVar_hsa_circ_210310,RMVar_hsa_circ_41038,RMVar_hsa_circ_29706,RMVar_hsa_circ_362777,RMVar_hsa_circ_210312,RMVar_hsa_circ_299348,RMVar_hsa_circ_324780,RMVar_hsa_circ_358561,RMVar_hsa_circ_318234,RMVar_hsa_circ_294719,RMVar_hsa_circ_210314,RMVar_hsa_circ_210316,RMVar_hsa_circ_210315,RMVar_hsa_circ_210313,RMVar_hsa_circ_11228 12942 RMVar_ID_12942 Human_SNP_ID_682048053 A-to-I Human chr20 - 44506044 44506044 44506044 CACCCATCTCAGCCTCCCAAAGTGCTGGTTTTACAGTTGTGAGCCACCGCATGTGGCTGGGAATG CACCCATCTCAGCCTCCCAAAGTGCTGGTTTTCCAGTTGTGAGCCACCGCATGTGGCTGGGAATG T G SERINC3 Ensembl:ENSG00000132824 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs963526312 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3803,RMVar_hsa_circ_96393,RMVar_hsa_circ_210310,RMVar_hsa_circ_41038,RMVar_hsa_circ_29706,RMVar_hsa_circ_362777,RMVar_hsa_circ_210312,RMVar_hsa_circ_299348,RMVar_hsa_circ_324780,RMVar_hsa_circ_358561,RMVar_hsa_circ_318234,RMVar_hsa_circ_294719,RMVar_hsa_circ_210314,RMVar_hsa_circ_210316,RMVar_hsa_circ_210315,RMVar_hsa_circ_210313,RMVar_hsa_circ_11228 12943 RMVar_ID_12943 Human_SNP_ID_682048076 A-to-I Human chr20 - 44506144 44506144 44506144 GGCGCCTGCCACCATGCCCGGCTAATTTTTGTATTTTTAGTTGAGACGGGGTTTCACCATGTTGG GGCGCCTGCCACCATGCCCGGCTAATTTTTGTGTTTTTAGTTGAGACGGGGTTTCACCATGTTGG T C SERINC3 Ensembl:ENSG00000132824 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1458347528 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3803,RMVar_hsa_circ_96393,RMVar_hsa_circ_210310,RMVar_hsa_circ_41038,RMVar_hsa_circ_29706,RMVar_hsa_circ_362777,RMVar_hsa_circ_210312,RMVar_hsa_circ_299348,RMVar_hsa_circ_324780,RMVar_hsa_circ_358561,RMVar_hsa_circ_318234,RMVar_hsa_circ_294719,RMVar_hsa_circ_210314,RMVar_hsa_circ_210316,RMVar_hsa_circ_210315,RMVar_hsa_circ_210313,RMVar_hsa_circ_11228 12944 RMVar_ID_12944 Human_SNP_ID_682048078 A-to-I Human chr20 - 44506152 44506152 44506152 CTTGGCCAGGCGCCTGCCACCATGCCCGGCTAATTTTTGTATTTTTAGTTGAGACGGGGTTTCAC CTTGGCCAGGCGCCTGCCACCATGCCCGGCTAGTTTTTGTATTTTTAGTTGAGACGGGGTTTCAC T C SERINC3 Ensembl:ENSG00000132824 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1187296552 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3803,RMVar_hsa_circ_96393,RMVar_hsa_circ_210310,RMVar_hsa_circ_41038,RMVar_hsa_circ_29706,RMVar_hsa_circ_362777,RMVar_hsa_circ_210312,RMVar_hsa_circ_299348,RMVar_hsa_circ_324780,RMVar_hsa_circ_358561,RMVar_hsa_circ_318234,RMVar_hsa_circ_294719,RMVar_hsa_circ_210314,RMVar_hsa_circ_210316,RMVar_hsa_circ_210315,RMVar_hsa_circ_210313,RMVar_hsa_circ_11228 12945 RMVar_ID_12945 Human_SNP_ID_682048090 A-to-I Human chr20 - 44506221 44506221 44506221 GCTGGAGTGCGATGGTGCAATCTCAGCTCACTACAACCTCCACCTCCTGGGTTCCAGTGATTCTC GCTGGAGTGCGATGGTGCAATCTCAGCTCACTGCAACCTCCACCTCCTGGGTTCCAGTGATTCTC T C SERINC3 Ensembl:ENSG00000132824 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs944272999 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3803,RMVar_hsa_circ_96393,RMVar_hsa_circ_210310,RMVar_hsa_circ_41038,RMVar_hsa_circ_29706,RMVar_hsa_circ_362777,RMVar_hsa_circ_210312,RMVar_hsa_circ_299348,RMVar_hsa_circ_324780,RMVar_hsa_circ_358561,RMVar_hsa_circ_318234,RMVar_hsa_circ_294719,RMVar_hsa_circ_210314,RMVar_hsa_circ_210316,RMVar_hsa_circ_210315,RMVar_hsa_circ_210313,RMVar_hsa_circ_11228 12946 RMVar_ID_12946 Human_SNP_ID_682077276 A-to-I Human chr20 - 44628279 44628279 44628279 CTCAGGTGATCTGCCCGCCTCGGCCTCCCAAAATGCTGGGATTACAGGCGTGAGCCACTGCGCCT CTCAGGTGATCTGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCGCCT T C ADA Ensembl:ENSG00000196839 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1202296397 Functional Loss SNV dbSNP153 33..33 33 - - - 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 12947 RMVar_ID_12947 Human_SNP_ID_682077322 A-to-I Human chr20 - 44628512 44628512 44628512 ATTTATTTATTTATTTATTGAGACAGAGTCTCACTCTGTTGCCCAGGCTGAAGTGCAGTGGTGCG ATTTATTTATTTATTTATTGAGACAGAGTCTCTCTCTGTTGCCCAGGCTGAAGTGCAGTGGTGCG T A ADA Ensembl:ENSG00000196839 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1350924420 Functional Loss SNV dbSNP153 33..33 33 - - - 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 12948 RMVar_ID_12948 Human_SNP_ID_682077761 A-to-I Human chr20 - 44630141 44630141 44630141 GGGGTTTCACCATGTTGGCCAGGATAGTCTCAATCTCCTGACCTCATGATCCTCGCACCTTGGCC GGGGTTTCACCATGTTGGCCAGGATAGTCTCACTCTCCTGACCTCATGATCCTCGCACCTTGGCC T G ADA Ensembl:ENSG00000196839 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1484257563 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118339,RMVar_hsa_circ_92423,RMVar_hsa_circ_210333,RMVar_hsa_circ_210332,RMVar_hsa_circ_210345,RMVar_hsa_circ_81724,RMVar_hsa_circ_85154,RMVar_hsa_circ_210344 12949 RMVar_ID_12949 Human_SNP_ID_682085486 A-to-I Human chr20 - 44662686 44662686 44662686 TTGCATGTTGACCAGGCTGGTCTCGAACTTTTAACCTCAAGTGATCCACCCGCCTTGGCCTCCCA TTGCATGTTGACCAGGCTGGTCTCGAACTTTTTACCTCAAGTGATCCACCCGCCTTGGCCTCCCA T A LINC01260,AL139352.1 Ensembl:ENSG00000283440,Ensembl:ENSG00000132832 lincRNA,lincRNA intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1394171499 Functional Loss SNV dbSNP153 33..33 33 - - - 12950 RMVar_ID_12950 Human_SNP_ID_682086905 A-to-I Human chr20 - 44668678 44668678 44668678 ACTCCTGGCTAACTTTAAAATTTTTATTTTGTAGAGACAAGGTCTCACTATGTTGCCCTGGCTGG ACTCCTGGCTAACTTTAAAATTTTTATTTTGTGGAGACAAGGTCTCACTATGTTGCCCTGGCTGG T C AL139352.1 Ensembl:ENSG00000132832 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1445022290 Functional Loss SNV dbSNP153 33..33 33 - - - 12951 RMVar_ID_12951 Human_SNP_ID_682100279 A-to-I Human chr20 + 44722608 44722608 44722608 CACGCCTCAGCCTCCCAAGTAGCTGGGATTACAGACACATACCACCATGCCTCGCTAATTTTTGT CACGCCTCAGCCTCCCAAGTAGCTGGGATTACGGACACATACCACCATGCCTCGCTAATTTTTGT A G CCN5 Ensembl:ENSG00000064205 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1462574991 Functional Loss SNV dbSNP153 33..33 33 - - - 12952 RMVar_ID_12952 Human_SNP_ID_682101652 A-to-I Human chr20 + 44728089 44728089 44728089 ACGATCTCGACTCACTGCAGCCTCCCGGGTTCAAGTGATTCTCCTGCCTCAAGACTCCTGAGTAG ACGATCTCGACTCACTGCAGCCTCCCGGGTTCTAGTGATTCTCCTGCCTCAAGACTCCTGAGTAG A T CCN5 Ensembl:ENSG00000064205 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1233746812 Functional Loss SNV dbSNP153 33..33 33 - - - 12953 RMVar_ID_12953 Human_SNP_ID_682152891 A-to-I Human chr20 + 44939179 44939179 44939179 TGGCTGCCAAAAGGACAGTGTTTCTGGCTCTCAGCCCTAAGGCCCTGCAAACTCTAACTTATTTC TGGCTGCCAAAAGGACAGTGTTTCTGGCTCTCGGCCCTAAGGCCCTGCAAACTCTAACTTATTTC A G PABPC1L Ensembl:ENSG00000101104 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1338308419 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1198514,Human_RBP_ID_1930379,Human_RBP_ID_8534197,Human_RBP_ID_14117619,Human_RBP_ID_18167699,Human_RBP_ID_18773916,Human_RBP_ID_25614423,Human_RBP_ID_27486205 Human_Splice_Rec_2087166,Human_Splice_Rec_2087194,Human_Splice_Rec_2087220,Human_Splice_Rec_2087246,Human_Splice_Rec_2087270,Human_Splice_Rec_2087292,Human_Splice_Rec_2087322,Human_Splice_Rec_2087334,Human_Splice_Rec_2087368,Human_Splice_Rec_2087376,Human_Splice_Rec_2087378 Human_miRNA_ID_1311081 12954 RMVar_ID_12954 Human_SNP_ID_682180331 A-to-I Human chr20 + 45059574 45059574 45059574 AGGGATGATTCACATCCCAAGCGGGATAGAGCAGGACAGCGCAGGATTTCATCATGCGTCTCAGA AGGGATGATTCACATCCCAAGCGGGATAGAGCGGGACAGCGCAGGATTTCATCATGCGTCTCAGA A G STK4 Ensembl:ENSG00000101109 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1393056909 Functional Loss SNV dbSNP153 33..33 33 - - - 12955 RMVar_ID_12955 Human_SNP_ID_682180694 A-to-I Human chr20 + 45061455 45061455 45061455 CTTGTGCCATCCTGCTCCATCCTGCCTGGGACATGAATCATTGCTCTGTTCAGCATATCCACTCG CTTGTGCCATCCTGCTCCATCCTGCCTGGGACGTGAATCATTGCTCTGTTCAGCATATCCACTCG A G STK4 Ensembl:ENSG00000101109 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1375563483 Functional Loss SNV dbSNP153 33..33 33 - - - 12956 RMVar_ID_12956 Human_SNP_ID_682183860 A-to-I Human chr20 + 45075946 45075946 45075946 CCTTTCATCCATCTCCACTCTCTCAACTGCCTAAAGTCACAGCACAGATACTGCCCAGTGCCTTA CCTTTCATCCATCTCCACTCTCTCAACTGCCTGAAGTCACAGCACAGATACTGCCCAGTGCCTTA A G STK4 Ensembl:ENSG00000101109 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs143954059 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17283470,Human_RBP_ID_18774003 12957 RMVar_ID_12957 Human_SNP_ID_682184380 A-to-I Human chr20 + 45078299 45078299 45078299 GCCATCTCGGCTCACTGCAACCTCCGCCTCCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCA GCCATCTCGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCA A G STK4 Ensembl:ENSG00000101109 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs1273164536 Functional Loss SNV dbSNP153 33..33 33 - - - 12958 RMVar_ID_12958 Human_SNP_ID_682184400 A-to-I Human chr20 + 45078404 45078404 45078404 AATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATATTAGCCAGGTGGGTCTTGAACTCCTGA AATTTTTGTATTTTTAGTAGAGACAGGGTTTCGCCATATTAGCCAGGTGGGTCTTGAACTCCTGA A G STK4 Ensembl:ENSG00000101109 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006805600 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14118946,Human_RBP_ID_23906956 12959 RMVar_ID_12959 Human_SNP_ID_682184556 A-to-I Human chr20 + 45079068 45079068 45079068 ATCTCTACAAAACATCAAAAAAAAAAAAAATTAGTCGGGCATGGTGGTGCACACCTGTAATCCCA ATCTCTACAAAACATCAAAAAAAAAAAAAATTTGTCGGGCATGGTGGTGCACACCTGTAATCCCA A T STK4 Ensembl:ENSG00000101109 Protein coding 3'UTR GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;ASD brains,temporal_cortex;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,30559470,31158229,31158229,32596459 RNA-Seq:(High) rs934099823 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26490840 12960 RMVar_ID_12960 Human_SNP_ID_682184572 A-to-I Human chr20 + 45079135 45079135 45079135 TTGTCAGGAGGCTGAAGTGGGAGGATCACCTGAGCCCAGGGAGGTCAAGGATGCAGTGAGCCATG TTGTCAGGAGGCTGAAGTGGGAGGATCACCTGGGCCCAGGGAGGTCAAGGATGCAGTGAGCCATG A G STK4 Ensembl:ENSG00000101109 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE99789;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;ASD brains,temporal_cortex;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,29129909,29796672,30559470,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs1233423790 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_149927,Human_RBP_ID_26490842 Human_miRNA_ID_678042,Human_miRNA_ID_1158727 12961 RMVar_ID_12961 Human_SNP_ID_682184574 A-to-I Human chr20 + 45079149 45079149 45079149 AAGTGGGAGGATCACCTGAGCCCAGGGAGGTCAAGGATGCAGTGAGCCATGGTCTCACCACTGCA AAGTGGGAGGATCACCTGAGCCCAGGGAGGTCGAGGATGCAGTGAGCCATGGTCTCACCACTGCA A G STK4 Ensembl:ENSG00000101109 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs3180210 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_149927,Human_RBP_ID_7005341 Human_miRNA_ID_468821,Human_miRNA_ID_606971,Human_miRNA_ID_1057867 12962 RMVar_ID_12962 Human_SNP_ID_682184586 A-to-I Human chr20 + 45079181 45079181 45079181 AAGGATGCAGTGAGCCATGGTCTCACCACTGCACTCTAGCCTGGGTGACAGAATGAGACCCCGTC AAGGATGCAGTGAGCCATGGTCTCACCACTGCGCTCTAGCCTGGGTGACAGAATGAGACCCCGTC A G STK4 Ensembl:ENSG00000101109 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs536097034 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_213276,Human_miRNA_ID_222810,Human_miRNA_ID_761328,Human_miRNA_ID_766239,Human_miRNA_ID_1072981,Human_miRNA_ID_1259338,Human_miRNA_ID_1325827 12963 RMVar_ID_12963 Human_SNP_ID_682224234 A-to-I Human chr20 - 45241384 45241384 45241384 CTCTTGCCTCGGCCTCCCGAGTAGCTGGGATTACGGGTGCCCTCCACCATGCCCAGCTAATTTTT CTCTTGCCTCGGCCTCCCGAGTAGCTGGGATTGCGGGTGCCCTCCACCATGCCCAGCTAATTTTT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1300915915 Functional Loss SNV dbSNP153 33..33 33 - - - 12964 RMVar_ID_12964 Human_SNP_ID_682246518 A-to-I Human chr20 - 45325878 45325878 45325878 GGTTTGCTTTCTTCAGGCTCTAGGGCTGTGCTATCCAATACAGTAACCACATGCGGCTGTTTAAA GGTTTGCTTTCTTCAGGCTCTAGGGCTGTGCTGTCCAATACAGTAACCACATGCGGCTGTTTAAA T C SDC4 Ensembl:ENSG00000124145 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1303322454 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_565021,Human_RBP_ID_5119381,Human_RBP_ID_8205009,Human_RBP_ID_8949277,Human_RBP_ID_17281689,Human_RBP_ID_20660789,Human_RBP_ID_22395225,Human_RBP_ID_23907027,Human_RBP_ID_26493116 RMVar_hsa_circ_101700,RMVar_hsa_circ_105720,RMVar_hsa_circ_102036,RMVar_hsa_circ_210383,RMVar_hsa_circ_210385,RMVar_hsa_circ_98878,RMVar_hsa_circ_210386,RMVar_hsa_circ_210384 12965 RMVar_ID_12965 Human_SNP_ID_682246519 A-to-I Human chr20 - 45325878 45325878 45325878 GGTTTGCTTTCTTCAGGCTCTAGGGCTGTGCTATCCAATACAGTAACCACATGCGGCTGTTTAAA GGTTTGCTTTCTTCAGGCTCTAGGGCTGTGCTCTCCAATACAGTAACCACATGCGGCTGTTTAAA T G SDC4 Ensembl:ENSG00000124145 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1303322454 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_565021,Human_RBP_ID_5119381,Human_RBP_ID_8205009,Human_RBP_ID_8949277,Human_RBP_ID_17281689,Human_RBP_ID_20660789,Human_RBP_ID_22395225,Human_RBP_ID_23907027,Human_RBP_ID_26493116 RMVar_hsa_circ_101700,RMVar_hsa_circ_105720,RMVar_hsa_circ_102036,RMVar_hsa_circ_210383,RMVar_hsa_circ_210385,RMVar_hsa_circ_98878,RMVar_hsa_circ_210386,RMVar_hsa_circ_210384 12966 RMVar_ID_12966 Human_SNP_ID_682248353 A-to-I Human chr20 - 45333486 45333486 45333486 TTTTGTATTTTCAGCAGAGACGGGGTTTCACTATGTTGGCCAGGCTGGTCTCGATCTCCTGACCT TTTTGTATTTTCAGCAGAGACGGGGTTTCACTGTGTTGGCCAGGCTGGTCTCGATCTCCTGACCT T C SDC4 Ensembl:ENSG00000124145 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs960879369 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101700,RMVar_hsa_circ_102036,RMVar_hsa_circ_210385,RMVar_hsa_circ_210386,RMVar_hsa_circ_23306,RMVar_hsa_circ_113437,RMVar_hsa_circ_312721,RMVar_hsa_circ_210389 12967 RMVar_ID_12967 Human_SNP_ID_682259885 A-to-I Human chr20 + 45381541 45381541 45381541 GTTGGCCAGGCTGGTTTCAAACTCCTGACCTCAAGTGATCTGCCCACCTCGGCCTCCCAAAGTGC GTTGGCCAGGCTGGTTTCAAACTCCTGACCTCGAGTGATCTGCCCACCTCGGCCTCCCAAAGTGC A G SYS1-DBNDD2 Ensembl:ENSG00000254806 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1421316811 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210390 12968 RMVar_ID_12968 Human_SNP_ID_682259978 A-to-I Human chr20 + 45381987 45381987 45381987 GGGAGACCGAGGCAGGTGGATCACCTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACACGGTGA GGGAGACCGAGGCAGGTGGATCACCTGAGGTCGGGAGTTCGAGACCAGCCTGGCCAACACGGTGA A G SYS1-DBNDD2 Ensembl:ENSG00000254806 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947011436 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210390 12969 RMVar_ID_12969 Human_SNP_ID_682261016 A-to-I Human chr20 + 45386593 45386593 45386593 TTCTAATTAGACTGTTTGGATGTTTGTTCTAGAAAAAGAGTCTTGCTCTGTCACCCAGGTTAGAG TTCTAATTAGACTGTTTGGATGTTTGTTCTAGGAAAAGAGTCTTGCTCTGTCACCCAGGTTAGAG A G SYS1-DBNDD2 Ensembl:ENSG00000254806 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs959550413 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210390 12970 RMVar_ID_12970 Human_SNP_ID_682269857 A-to-I Human chr20 + 45422502 45422502 45422502 AGACTGTTGCTCTGTCAGCTATGCCGGAGTGCAGTGGCATGATCATGGCTCATTGCAGTCTCAGA AGACTGTTGCTCTGTCAGCTATGCCGGAGTGCGGTGGCATGATCATGGCTCATTGCAGTCTCAGA A G PIGT Ensembl:ENSG00000124155 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1568951748 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14119616,Human_RBP_ID_22506720 RMVar_hsa_circ_49921,RMVar_hsa_circ_53277,RMVar_hsa_circ_325165 12971 RMVar_ID_12971 Human_SNP_ID_682269876 A-to-I Human chr20 + 45422585 45422585 45422585 CCTCCTACCTCCGCTTCCCTAGGACTACAGGCATGAACCGCCATGCCTTTAATTTTTTCACAGAG CCTCCTACCTCCGCTTCCCTAGGACTACAGGCCTGAACCGCCATGCCTTTAATTTTTTCACAGAG A C PIGT Ensembl:ENSG00000124155 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1024805777 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7005653,Human_RBP_ID_14119618 RMVar_hsa_circ_49921,RMVar_hsa_circ_53277,RMVar_hsa_circ_325165 12972 RMVar_ID_12972 Human_SNP_ID_682274867 A-to-I Human chr20 + 45441951 45441951 45441951 GACATTAGCACTAACATAGACCTTAAGCTGATAAGCATTTACAACCTCTTCTCTCTGAAGCCTGC GACATTAGCACTAACATAGACCTTAAGCTGATGAGCATTTACAACCTCTTCTCTCTGAAGCCTGC A G PIGT Ensembl:ENSG00000124155 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs905663561 Functional Loss SNV dbSNP153 33..33 33 - - - 12973 RMVar_ID_12973 Human_SNP_ID_682274868 A-to-I Human chr20 + 45441951 45441951 45441951 GACATTAGCACTAACATAGACCTTAAGCTGATAAGCATTTACAACCTCTTCTCTCTGAAGCCTGC GACATTAGCACTAACATAGACCTTAAGCTGATTAGCATTTACAACCTCTTCTCTCTGAAGCCTGC A T PIGT Ensembl:ENSG00000124155 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs905663561 Functional Loss SNV dbSNP153 33..33 33 - - - 12974 RMVar_ID_12974 Human_SNP_ID_682274888 A-to-I Human chr20 + 45442025 45442025 45442025 GGCTTCATCTGCATGATGAAACCTTGGTCTCCACAACCCCTTACCTAACCCAGACATTCCTTTCT GGCTTCATCTGCATGATGAAACCTTGGTCTCCGCAACCCCTTACCTAACCCAGACATTCCTTTCT A G PIGT Ensembl:ENSG00000124155 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs750826105 Functional Loss SNV dbSNP153 33..33 33 - - - 12975 RMVar_ID_12975 Human_SNP_ID_682365844 A-to-I Human chr20 + 45814037 45814036 45814038 TGAGGCACAAGAATCATTTGAACCGTGGAGACAGAGGTTGCGGTGAGCCGAGCGCACCACTGCAC TGAGGCACAAGAATCATTTGAACCGTGGAGAC__AGGTTGCGGTGAGCCGAGCGCACCACTGCAC CAG C UBE2C Ensembl:ENSG00000175063 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1439364883 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_14120135 RMVar_hsa_circ_89472,RMVar_hsa_circ_210396 12976 RMVar_ID_12976 Human_SNP_ID_682366355 A-to-I Human chr20 + 45815257 45815256 45815257 AGGAAAGCATCAGGCTAGGCATAGTGGCTCACACCTGTAATCTCAGCACTTTGGGAGGCTGAGGC AGGAAAGCATCAGGCTAGGCATAGTGGCTCAC_CCTGTAATCTCAGCACTTTGGGAGGCTGAGGC CA C UBE2C Ensembl:ENSG00000175063 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1352487267 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_89472,RMVar_hsa_circ_123205,RMVar_hsa_circ_210396,RMVar_hsa_circ_210397 12977 RMVar_ID_12977 Human_SNP_ID_682372081 A-to-I Human chr20 + 45836543 45836543 45836543 AAAAAAATTTTGAGACAGGGTCTCGTTCTGTCACTCAGGCTGGAGTGCAGTGGTGCAGTCATAAC AAAAAAATTTTGAGACAGGGTCTCGTTCTGTCCCTCAGGCTGGAGTGCAGTGGTGCAGTCATAAC A C SNX21 Ensembl:ENSG00000124104 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355024722 Functional Loss SNV dbSNP153 33..33 33 - - - 12978 RMVar_ID_12978 Human_SNP_ID_682372092 A-to-I Human chr20 + 45836581 45836581 45836581 GCTGGAGTGCAGTGGTGCAGTCATAACTCACTACAACCTCCAACTGGGCTCAAGCTATCCTCCCA GCTGGAGTGCAGTGGTGCAGTCATAACTCACTGCAACCTCCAACTGGGCTCAAGCTATCCTCCCA A G SNX21 Ensembl:ENSG00000124104 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1481196738 Functional Loss SNV dbSNP153 33..33 33 - - - 12979 RMVar_ID_12979 Human_SNP_ID_682372687 A-to-I Human chr20 + 45839093 45839091 45839093 TTTTGCATTTTTAGTAGAGACAGGGTTTCTCCATGTTGGTCAGCCTGGTCTCGAACTCTCAACCT TTTTGCATTTTTAGTAGAGACAGGGTTTCTC__TGTTGGTCAGCCTGGTCTCGAACTCTCAACCT CCA C SNX21 Ensembl:ENSG00000124104 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1449270750 Functional Loss DEL dbSNP153 32..33 33 - - - 12980 RMVar_ID_12980 Human_SNP_ID_682375257 A-to-I Human chr20 + 45848011 45848011 45848011 GTTGCCCAGGCTGGTCTTGAACTCCTGGGCTCAGGTGATCCTCCCACTTGGGCTTCCCAAAGTGT GTTGCCCAGGCTGGTCTTGAACTCCTGGGCTCCGGTGATCCTCCCACTTGGGCTTCCCAAAGTGT A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1216977538 Functional Loss SNV dbSNP153 33..33 33 - - - 12981 RMVar_ID_12981 Human_SNP_ID_682375819 A-to-I Human chr20 - 45850235 45850235 45850235 GGATGTCCCACTCTTTTTTGAGACAGAGTTTCACTCTTGTTCCCCAGGCTGGAGTGCAGTGGTGC GGATGTCCCACTCTTTTTTGAGACAGAGTTTCCCTCTTGTTCCCCAGGCTGGAGTGCAGTGGTGC T G ACOT8 Ensembl:ENSG00000101473 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1229391192 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_313865,RMVar_hsa_circ_210404,RMVar_hsa_circ_300049,RMVar_hsa_circ_271536,RMVar_hsa_circ_210403 12982 RMVar_ID_12982 Human_SNP_ID_682376759 A-to-I Human chr20 - 45854277 45854277 45854277 TGAACCCGGAAGGCGGAGCTTGCAGTGAGCCAAGATCGTGCCACTGCACTCCAGCCTGGGCGAGC TGAACCCGGAAGGCGGAGCTTGCAGTGAGCCAGGATCGTGCCACTGCACTCCAGCCTGGGCGAGC T C ACOT8 Ensembl:ENSG00000101473 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054421499 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_313865,RMVar_hsa_circ_210404,RMVar_hsa_circ_271536,RMVar_hsa_circ_210405,RMVar_hsa_circ_305454 12983 RMVar_ID_12983 Human_SNP_ID_682384864 A-to-I Human chr20 - 45884501 45884501 45884501 AAAATTAGCCCGGCATTGTGGCGGGCGCCTGTAGTCCCAGATACTCGGGAGGCTGAGGCAGGAGA AAAATTAGCCCGGCATTGTGGCGGGCGCCTGTGGTCCCAGATACTCGGGAGGCTGAGGCAGGAGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1379206912 Functional Loss SNV dbSNP153 33..33 33 - - - 12984 RMVar_ID_12984 Human_SNP_ID_682384884 A-to-I Human chr20 + 45884544 45884544 45884544 GCCACAATGCCGGGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGA GCCACAATGCCGGGCTAATTTTTTGTATTTTTGGTAGAGACGGGGTTTCACCGTGTTAGCCAGGA A G ZSWIM1 Ensembl:ENSG00000168612 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1013929465 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119690,RMVar_hsa_circ_210406 12985 RMVar_ID_12985 Human_SNP_ID_682384895 A-to-I Human chr20 + 45884569 45884569 45884569 TATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGGTCTCGATCTCCTGACTTCGTGA TATTTTTAGTAGAGACGGGGTTTCACCGTGTTGGCCAGGATGGTCTCGATCTCCTGACTTCGTGA A G ZSWIM1 Ensembl:ENSG00000168612 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs961300872 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119690,RMVar_hsa_circ_210406 12986 RMVar_ID_12986 Human_SNP_ID_682384958 A-to-I Human chr20 - 45884776 45884776 45884776 GAACTCCTGACCTCAAGTCATCTGTCCACCTCAGCCTCCCAAAATGCTGGGATTACAGGCGTGAG GAACTCCTGACCTCAAGTCATCTGTCCACCTCGGCCTCCCAAAATGCTGGGATTACAGGCGTGAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs922602471 Functional Loss SNV dbSNP153 33..33 33 - - - 12987 RMVar_ID_12987 Human_SNP_ID_682384961 A-to-I Human chr20 - 45884781 45884781 45884781 GTCTTGAACTCCTGACCTCAAGTCATCTGTCCACCTCAGCCTCCCAAAATGCTGGGATTACAGGC GTCTTGAACTCCTGACCTCAAGTCATCTGTCCGCCTCAGCCTCCCAAAATGCTGGGATTACAGGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs955395903 Functional Loss SNV dbSNP153 33..33 33 - - - 12988 RMVar_ID_12988 Human_SNP_ID_682388227 A-to-I Human chr20 + 45895042 45895042 45895042 GGGATAAAGTGCGCATGGACCCCCCCTGCACCAACACAACAGCTGCTTCCACCTACCTCAACAAC GGGATAAAGTGCGCATGGACCCCCCCTGCACCGACACAACAGCTGCTTCCACCTACCTCAACAAC A G CTSA Ensembl:ENSG00000064601 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs112880409 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17511886,Human_RBP_ID_17976981,Human_RBP_ID_22453124,Human_RBP_ID_27488964,Human_RBP_ID_27564617 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 12989 RMVar_ID_12989 Human_SNP_ID_682388399 A-to-I Human chr20 + 45895658 45895658 45895658 TAGCCACATTGGTTGTTGTTTCACAGTTCACTACAGCCTCAACCTCCTAGGCTCAAGCGATCCTC TAGCCACATTGGTTGTTGTTTCACAGTTCACTGCAGCCTCAACCTCCTAGGCTCAAGCGATCCTC A G CTSA Ensembl:ENSG00000064601 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs61241783 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17972739 RMVar_hsa_circ_296311,RMVar_hsa_circ_210408,RMVar_hsa_circ_15011,RMVar_hsa_circ_32000 12990 RMVar_ID_12990 Human_SNP_ID_682388401 A-to-I Human chr20 + 45895660 45895660 45895660 GCCACATTGGTTGTTGTTTCACAGTTCACTACAGCCTCAACCTCCTAGGCTCAAGCGATCCTCCC GCCACATTGGTTGTTGTTTCACAGTTCACTACGGCCTCAACCTCCTAGGCTCAAGCGATCCTCCC A G CTSA Ensembl:ENSG00000064601 Protein coding intron GSE47997;GSE38233;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,32596459 RNA-Seq:(High) rs1250169193 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17972739 RMVar_hsa_circ_296311,RMVar_hsa_circ_210408,RMVar_hsa_circ_15011,RMVar_hsa_circ_32000 12991 RMVar_ID_12991 Human_SNP_ID_682388403 A-to-I Human chr20 + 45895674 45895671 45895675 TGTTTCACAGTTCACTACAGCCTCAACCTCCTAGGCTCAAGCGATCCTCCCACCTTAGTCTACTG TGTTTCACAGTTCACTACAGCCTCAACCTC____GCTCAAGCGATCCTCCCACCTTAGTCTACTG CCTAG C CTSA Ensembl:ENSG00000064601 Protein coding intron GSE47997;GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,29129909,31158229,31158229,32596459 RNA-Seq:(High) rs1212133558 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_17571644,Human_RBP_ID_17972739 RMVar_hsa_circ_296311,RMVar_hsa_circ_210408,RMVar_hsa_circ_15011,RMVar_hsa_circ_32000 12992 RMVar_ID_12992 Human_SNP_ID_682388429 A-to-I Human chr20 + 45895774 45895774 45895774 GGCTAATTTTTAAAAAATTTTTTTGTAGAGACAGGGTCTCACTATGTTGTCCAGGTTGGTCTCAA GGCTAATTTTTAAAAAATTTTTTTGTAGAGACGGGGTCTCACTATGTTGTCCAGGTTGGTCTCAA A G CTSA Ensembl:ENSG00000064601 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1436530752 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571645 RMVar_hsa_circ_296311,RMVar_hsa_circ_210408,RMVar_hsa_circ_15011,RMVar_hsa_circ_32000 12993 RMVar_ID_12993 Human_SNP_ID_682388432 A-to-I Human chr20 + 45895785 45895785 45895785 AAAAAATTTTTTTGTAGAGACAGGGTCTCACTATGTTGTCCAGGTTGGTCTCAAACTCTTGGTCT AAAAAATTTTTTTGTAGAGACAGGGTCTCACTGTGTTGTCCAGGTTGGTCTCAAACTCTTGGTCT A G CTSA Ensembl:ENSG00000064601 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1343697543 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571645 RMVar_hsa_circ_296311,RMVar_hsa_circ_210408,RMVar_hsa_circ_15011,RMVar_hsa_circ_32000 12994 RMVar_ID_12994 Human_SNP_ID_682396561 A-to-I Human chr20 - 45926756 45926756 45926756 GGATGCCAAAGTGGGAGGATTGCTTGTGGCCAAAAGTTCAAGACCAGCATGTGCAACATAGAACC GGATGCCAAAGTGGGAGGATTGCTTGTGGCCACAAGTTCAAGACCAGCATGTGCAACATAGAACC T G AL162458.1 Ensembl:ENSG00000285796 lincRNA exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1294522370 Functional Loss SNV dbSNP153 33..33 33 - - - 12995 RMVar_ID_12995 Human_SNP_ID_682396662 A-to-I Human chr20 - 45927200 45927200 45927200 GGGTTTCACCGTGTTGACCAGGCTGGCCTCGAACTCCTGACCTCAAGCAATCTGCCTGCCTCGGC GGGTTTCACCGTGTTGACCAGGCTGGCCTCGATCTCCTGACCTCAAGCAATCTGCCTGCCTCGGC T A AL162458.1 Ensembl:ENSG00000285796 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs970902042 Functional Loss SNV dbSNP153 33..33 33 - - - 12996 RMVar_ID_12996 Human_SNP_ID_682397842 A-to-I Human chr20 - 45931552 45931552 45931552 CCTGGCCAACAGGGTGAAAGCCCATCTGTACTAAAAATACAAAAATTAGCTGGGCATGGTGGCAA CCTGGCCAACAGGGTGAAAGCCCATCTGTACTGAAAATACAAAAATTAGCTGGGCATGGTGGCAA T C AL162458.1 Ensembl:ENSG00000285796 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1468745368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23311463 12997 RMVar_ID_12997 Human_SNP_ID_682405912 A-to-I Human chr20 - 45954900 45954900 45954900 AGCCGGGTGTGGCAATGCATGCCTGTAGTACCAGCTACTTGAGAGGCTGAGGTGGGAGGATCGCT AGCCGGGTGTGGCAATGCATGCCTGTAGTACCGGCTACTTGAGAGGCTGAGGTGGGAGGATCGCT T C ZNF335 Ensembl:ENSG00000198026 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1568810995 Functional Loss SNV dbSNP153 33..33 33 - - - 12998 RMVar_ID_12998 Human_SNP_ID_682405925 A-to-I Human chr20 - 45954960 45954960 45954960 GAGTCCAGGAGTTTGAGACCAGCCTGGACAACATGGTGAAACCCTGTCTCTTAAAAAATTAGCCG GAGTCCAGGAGTTTGAGACCAGCCTGGACAACGTGGTGAAACCCTGTCTCTTAAAAAATTAGCCG T C ZNF335 Ensembl:ENSG00000198026 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs533362406 Functional Loss SNV dbSNP153 33..33 33 - - - 12999 RMVar_ID_12999 Human_SNP_ID_682405992 A-to-I Human chr20 - 45955232 45955232 45955232 ATTCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGACACCCACCACCACGACTGGCTTCTTTTA ATTCTGCCTCAGCCTCCCAAGTAGCTGGGACTGCAGACACCCACCACCACGACTGGCTTCTTTTA T C ZNF335 Ensembl:ENSG00000198026 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs534905267 Functional Loss SNV dbSNP153 33..33 33 - - - 13000 RMVar_ID_13000 Human_SNP_ID_682405997 A-to-I Human chr20 - 45955254 45955254 45955254 CTCCGCCTCCCGGGTTCACACCATTCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGACACCCA CTCCGCCTCCCGGGTTCACACCATTCTGCCTCCGCCTCCCAAGTAGCTGGGACTACAGACACCCA T G ZNF335 Ensembl:ENSG00000198026 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs973175883 Functional Loss SNV dbSNP153 33..33 33 - - - 13001 RMVar_ID_13001 Human_SNP_ID_682406005 A-to-I Human chr20 - 45955288 45955288 45955288 GGAGTGCAGTGGTGCGATCTCGGCTCACTGCAACCTCCGCCTCCCGGGTTCACACCATTCTGCCT GGAGTGCAGTGGTGCGATCTCGGCTCACTGCAGCCTCCGCCTCCCGGGTTCACACCATTCTGCCT T C ZNF335 Ensembl:ENSG00000198026 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs937699462 Functional Loss SNV dbSNP153 33..33 33 - - - 13002 RMVar_ID_13002 Human_SNP_ID_682406006 A-to-I Human chr20 - 45955288 45955288 45955288 GGAGTGCAGTGGTGCGATCTCGGCTCACTGCAACCTCCGCCTCCCGGGTTCACACCATTCTGCCT GGAGTGCAGTGGTGCGATCTCGGCTCACTGCACCCTCCGCCTCCCGGGTTCACACCATTCTGCCT T G ZNF335 Ensembl:ENSG00000198026 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs937699462 Functional Loss SNV dbSNP153 33..33 33 - - - 13003 RMVar_ID_13003 Human_SNP_ID_682406135 A-to-I Human chr20 - 45955634 45955634 45955634 TTGTATTTTTAGTAGGGATAGGGTTTCACCATATTGGCCAGGCTAGTTTCGAACTCCTGACCTCA TTGTATTTTTAGTAGGGATAGGGTTTCACCATGTTGGCCAGGCTAGTTTCGAACTCCTGACCTCA T C ZNF335 Ensembl:ENSG00000198026 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs867092260 Functional Loss SNV dbSNP153 33..33 33 - - - 13004 RMVar_ID_13004 Human_SNP_ID_682406170 A-to-I Human chr20 - 45955758 45955758 45955758 TGGAGTGCAGTGGCGTGATGTTGGCTCCCTGCAACCTCCGCCTCCTGGGTTCAAATGATTGTCCT TGGAGTGCAGTGGCGTGATGTTGGCTCCCTGCGACCTCCGCCTCCTGGGTTCAAATGATTGTCCT T C ZNF335 Ensembl:ENSG00000198026 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1199033586 Functional Loss SNV dbSNP153 33..33 33 - - - 13005 RMVar_ID_13005 Human_SNP_ID_682406338 A-to-I Human chr20 - 45956361 45956361 45956361 AGCTGGGCGTGGTGGCACACGTCTGTAATCCCAGCCACTCGGGAGGCCGAGGCAGGAGAATCGCT AGCTGGGCGTGGTGGCACACGTCTGTAATCCCTGCCACTCGGGAGGCCGAGGCAGGAGAATCGCT T A ZNF335 Ensembl:ENSG00000198026 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1352305438 Functional Loss SNV dbSNP153 33..33 33 - - - 13006 RMVar_ID_13006 Human_SNP_ID_682451318 A-to-I Human chr20 + 46124043 46124043 46124043 GCCCCAGGCCAGGCGCGGTGGCTCTTGCCTGTAATCTCAGCACTTTGGATGCCAAGGCGGGTGGA GCCCCAGGCCAGGCGCGGTGGCTCTTGCCTGTCATCTCAGCACTTTGGATGCCAAGGCGGGTGGA A C CD40 Ensembl:ENSG00000101017 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs972410339 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20661456 13007 RMVar_ID_13007 Human_SNP_ID_682451336 A-to-I Human chr20 + 46124111 46124111 46124111 CTTGAGGTCAGGAGTTCAAGACCAGCCAGCACAACATGGTAAAAACCCATCTCTACTAAAAATAC CTTGAGGTCAGGAGTTCAAGACCAGCCAGCACGACATGGTAAAAACCCATCTCTACTAAAAATAC A G CD40 Ensembl:ENSG00000101017 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs936193385 Functional Loss SNV dbSNP153 33..33 33 - - - 13008 RMVar_ID_13008 Human_SNP_ID_682451373 A-to-I Human chr20 + 46124249 46124249 46124249 TTGAACCCGGAAGGTGGAGTTTGCAGTGAGCCAAGATAGCGCCACTGCACTCCAGCCTGGGCAAC TTGAACCCGGAAGGTGGAGTTTGCAGTGAGCCGAGATAGCGCCACTGCACTCCAGCCTGGGCAAC A G CD40 Ensembl:ENSG00000101017 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1219179037 Functional Loss SNV dbSNP153 33..33 33 - - - 13009 RMVar_ID_13009 Human_SNP_ID_682477379 A-to-I Human chr20 - 46229341 46229341 46229341 CCACCACTTCCTCACTCTGTGCCCTCAGTGAAATCTTTTCCCCTGTCTGACTTGATTCCTCAGCT CCACCACTTCCTCACTCTGTGCCCTCAGTGAATTCTTTTCCCCTGTCTGACTTGATTCCTCAGCT T A CDH22 Ensembl:ENSG00000149654 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1052701180 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24378,RMVar_hsa_circ_210437,RMVar_hsa_circ_377427 13010 RMVar_ID_13010 Human_SNP_ID_682477380 A-to-I Human chr20 - 46229341 46229341 46229341 CCACCACTTCCTCACTCTGTGCCCTCAGTGAAATCTTTTCCCCTGTCTGACTTGATTCCTCAGCT CCACCACTTCCTCACTCTGTGCCCTCAGTGAAGTCTTTTCCCCTGTCTGACTTGATTCCTCAGCT T C CDH22 Ensembl:ENSG00000149654 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1052701180 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24378,RMVar_hsa_circ_210437,RMVar_hsa_circ_377427 13011 RMVar_ID_13011 Human_SNP_ID_682505720 A-to-I Human chr20 - 46350169 46350169 46350169 GGCCAGCCTGGGACTGGCCAGAGCTGGGCCCAAGCTGCGCTGGAATCGCAGCAGGAGAGGGGAGT GGCCAGCCTGGGACTGGCCAGAGCTGGGCCCAGGCTGCGCTGGAATCGCAGCAGGAGAGGGGAGT T C SLC35C2 Ensembl:ENSG00000080189 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs966856763 Functional Loss SNV dbSNP153 33..33 33 - - - 13012 RMVar_ID_13012 Human_SNP_ID_682716422 A-to-I Human chr20 - 47214551 47214546 47214552 AGGCGGAGGTTACAGTGAGTTGAGACCGTGCCACTGCATTCCAGTCTGGGCGACAGAGTGAGACT AGGCGGAGGTTACAGTGAGTTGAGACCGTGC______ATTCCAGTCTGGGCGACAGAGTGAGACT TGCAGTG T ZMYND8 Ensembl:ENSG00000101040 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1191699494 Functional Loss DEL dbSNP153 32..37 33 - - - Human_RBP_ID_25615475 13013 RMVar_ID_13013 Human_SNP_ID_682716429 A-to-I Human chr20 - 47214572 47214572 47214572 TGAGAATTACTTGAACCCAGGAGGCGGAGGTTACAGTGAGTTGAGACCGTGCCACTGCATTCCAG TGAGAATTACTTGAACCCAGGAGGCGGAGGTTGCAGTGAGTTGAGACCGTGCCACTGCATTCCAG T C ZMYND8 Ensembl:ENSG00000101040 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs535958547 Functional Loss SNV dbSNP153 33..33 33 - - - 13014 RMVar_ID_13014 Human_SNP_ID_682716485 A-to-I Human chr20 - 47214761 47214761 47214761 GTCAGGCGTGGTGGCTCATGCCTATAATCCCAACACCTTGAGAGGCCAAGGTGGGTGGATCATTT GTCAGGCGTGGTGGCTCATGCCTATAATCCCAGCACCTTGAGAGGCCAAGGTGGGTGGATCATTT T C ZMYND8 Ensembl:ENSG00000101040 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1313172761 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571650 13015 RMVar_ID_13015 Human_SNP_ID_682716487 A-to-I Human chr20 - 47214770 47214770 47214770 CGCATTTAGGTCAGGCGTGGTGGCTCATGCCTATAATCCCAACACCTTGAGAGGCCAAGGTGGGT CGCATTTAGGTCAGGCGTGGTGGCTCATGCCTGTAATCCCAACACCTTGAGAGGCCAAGGTGGGT T C ZMYND8 Ensembl:ENSG00000101040 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1376687931 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571650,Human_RBP_ID_25615478 13016 RMVar_ID_13016 Human_SNP_ID_682716570 A-to-I Human chr20 - 47215049 47215049 47215049 AATTCTAAATGTTGTTTTGAAACCTAAGAGACAGGATCTTGCCTTGTTGCCGAGGCTGGCCTTGA AATTCTAAATGTTGTTTTGAAACCTAAGAGACGGGATCTTGCCTTGTTGCCGAGGCTGGCCTTGA T C ZMYND8 Ensembl:ENSG00000101040 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1229690633 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571908 13017 RMVar_ID_13017 Human_SNP_ID_682716729 A-to-I Human chr20 - 47215601 47215573 47215601 GAGAGGCTGAGTCAGGGGGGTTACTTGAGCCTAGGAGTTTTGAGACTGCAGTGAGTGCCTGTGAA GAGAGGCTGAGTCAGGGGGGTTACTTGAGCCT____________________________GTGAA CAGGCACTCACTGCAGTCTCAAAACTCCT C ZMYND8 Ensembl:ENSG00000101040 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1313105177 Functional Loss DEL dbSNP153 33..60 33 - - - 13018 RMVar_ID_13018 Human_SNP_ID_682717662 A-to-I Human chr20 - 47219048 47219048 47219048 CTCTCAAAAAAAAAAAAAAAAAAAATTGTAGAAACGGGGTTTTGCCATGTTGGCCAGGTTGGTCT CTCTCAAAAAAAAAAAAAAAAAAAATTGTAGAGACGGGGTTTTGCCATGTTGGCCAGGTTGGTCT T C ZMYND8 Ensembl:ENSG00000101040 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1021607502 Functional Loss SNV dbSNP153 33..33 33 - - - 13019 RMVar_ID_13019 Human_SNP_ID_682718483 A-to-I Human chr20 - 47221752 47221752 47221752 TGAGACAAGAGAATCACTTGAACCCAGGAGACAGAGGTTGCAGTGAGCTGAGATCGTGCCATTGC TGAGACAAGAGAATCACTTGAACCCAGGAGACCGAGGTTGCAGTGAGCTGAGATCGTGCCATTGC T G ZMYND8 Ensembl:ENSG00000101040 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs539301814 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2074,RMVar_hsa_circ_50712,RMVar_hsa_circ_295620,RMVar_hsa_circ_337898,RMVar_hsa_circ_73732,RMVar_hsa_circ_27426,RMVar_hsa_circ_349408,RMVar_hsa_circ_4641 13020 RMVar_ID_13020 Human_SNP_ID_682718489 A-to-I Human chr20 - 47221777 47221777 47221777 CCTGAGTCCCAGCTACTTGGTGGGCTGAGACAAGAGAATCACTTGAACCCAGGAGACAGAGGTTG CCTGAGTCCCAGCTACTTGGTGGGCTGAGACAGGAGAATCACTTGAACCCAGGAGACAGAGGTTG T C ZMYND8 Ensembl:ENSG00000101040 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs960547402 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26761686 RMVar_hsa_circ_2074,RMVar_hsa_circ_50712,RMVar_hsa_circ_295620,RMVar_hsa_circ_337898,RMVar_hsa_circ_73732,RMVar_hsa_circ_27426,RMVar_hsa_circ_349408,RMVar_hsa_circ_4641 13021 RMVar_ID_13021 Human_SNP_ID_682723301 A-to-I Human chr20 - 47240335 47240335 47240335 TATTTTTGTATTTTCGGTAGAGACGGGGTTTCACTATGTTGGCCAGGCTGCTCTTGAACTCCTGA TATTTTTGTATTTTCGGTAGAGACGGGGTTTCGCTATGTTGGCCAGGCTGCTCTTGAACTCCTGA T C ZMYND8 Ensembl:ENSG00000101040 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1473114025 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_347632,RMVar_hsa_circ_72108,RMVar_hsa_circ_91774,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 13022 RMVar_ID_13022 Human_SNP_ID_682723339 A-to-I Human chr20 - 47240475 47240475 47240475 GAGTCTCACCCTGTCACCCAGGCTGGAGTGCAATGGCATGGTCTCGGCTCCCTGCAACCTCCACG GAGTCTCACCCTGTCACCCAGGCTGGAGTGCAGTGGCATGGTCTCGGCTCCCTGCAACCTCCACG T C ZMYND8 Ensembl:ENSG00000101040 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs993467225 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_347632,RMVar_hsa_circ_72108,RMVar_hsa_circ_91774,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 13023 RMVar_ID_13023 Human_SNP_ID_682723411 A-to-I Human chr20 - 47240719 47240719 47240719 AAACCCCGTCTCTGCTGAAAATAAAAAAAATTAGCTGGGTGCGGTGGCAGGCGCCTGTAATCCCA AAACCCCGTCTCTGCTGAAAATAAAAAAAATTGGCTGGGTGCGGTGGCAGGCGCCTGTAATCCCA T C ZMYND8 Ensembl:ENSG00000101040 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs771992963 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25630723 RMVar_hsa_circ_73732,RMVar_hsa_circ_4641,RMVar_hsa_circ_70850,RMVar_hsa_circ_22992,RMVar_hsa_circ_44852,RMVar_hsa_circ_347632,RMVar_hsa_circ_72108,RMVar_hsa_circ_91774,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 13024 RMVar_ID_13024 Human_SNP_ID_682723434 A-to-I Human chr20 - 47240813 47240813 47240813 ACGTTGGCTCACGCCTGTAATTCCAGCACTTTAGGAGGCCAAGGCGGATGGATCATGAGGTCAGG ACGTTGGCTCACGCCTGTAATTCCAGCACTTTGGGAGGCCAAGGCGGATGGATCATGAGGTCAGG T C ZMYND8 Ensembl:ENSG00000101040 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs139314351 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22722946,Human_RBP_ID_25615593 RMVar_hsa_circ_73732,RMVar_hsa_circ_4641,RMVar_hsa_circ_70850,RMVar_hsa_circ_22992,RMVar_hsa_circ_44852,RMVar_hsa_circ_347632,RMVar_hsa_circ_72108,RMVar_hsa_circ_91774,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 13025 RMVar_ID_13025 Human_SNP_ID_682723525 A-to-I Human chr20 - 47241114 47241114 47241114 ATTTTTTGTATCTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGACTGGTTTCGAACTCCTGA ATTTTTTGTATCTTTAGTAGAGATGGGGTTTCCCCATGTTGGCCAGACTGGTTTCGAACTCCTGA T G ZMYND8 Ensembl:ENSG00000101040 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1232470832 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_347632,RMVar_hsa_circ_72108,RMVar_hsa_circ_91774,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 13026 RMVar_ID_13026 Human_SNP_ID_682723553 A-to-I Human chr20 - 47241213 47241213 47241213 TCGGCTCACTGCAACCTCTGCCTCATGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGC TCGGCTCACTGCAACCTCTGCCTCATGGGTTCGAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGC T C ZMYND8 Ensembl:ENSG00000101040 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1333966006 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_347632,RMVar_hsa_circ_72108,RMVar_hsa_circ_91774,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 13027 RMVar_ID_13027 Human_SNP_ID_682723562 A-to-I Human chr20 - 47241256 47241256 47241256 GAGTCTCGCCCTGTCACCCAGGCTGGAGTGCAATGGGGCGATTTCGGCTCACTGCAACCTCTGCC GAGTCTCGCCCTGTCACCCAGGCTGGAGTGCAGTGGGGCGATTTCGGCTCACTGCAACCTCTGCC T C ZMYND8 Ensembl:ENSG00000101040 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs555597856 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14122350 RMVar_hsa_circ_73732,RMVar_hsa_circ_4641,RMVar_hsa_circ_70850,RMVar_hsa_circ_22992,RMVar_hsa_circ_44852,RMVar_hsa_circ_347632,RMVar_hsa_circ_72108,RMVar_hsa_circ_91774,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 13028 RMVar_ID_13028 Human_SNP_ID_682729584 A-to-I Human chr20 - 47264459 47264459 47264459 CAGCCTGGCCAACATGGTAAAACCCTGTCTCTAGTAAAAATATAAAAAATAGCCGGGTGTGATAG CAGCCTGGCCAACATGGTAAAACCCTGTCTCTCGTAAAAATATAAAAAATAGCCGGGTGTGATAG T G ZMYND8 Ensembl:ENSG00000101040 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1255050784 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210488,RMVar_hsa_circ_3666,RMVar_hsa_circ_73732,RMVar_hsa_circ_4641,RMVar_hsa_circ_117845,RMVar_hsa_circ_82182,RMVar_hsa_circ_210472,RMVar_hsa_circ_210473,RMVar_hsa_circ_300845,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_281763,RMVar_hsa_circ_62862,RMVar_hsa_circ_87810,RMVar_hsa_circ_210482,RMVar_hsa_circ_210484,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_270363,RMVar_hsa_circ_210492,RMVar_hsa_circ_77505,RMVar_hsa_circ_96252,RMVar_hsa_circ_210494,RMVar_hsa_circ_210495,RMVar_hsa_circ_210493,RMVar_hsa_circ_210490,RMVar_hsa_circ_210491,RMVar_hsa_circ_210489,RMVar_hsa_circ_210486,RMVar_hsa_circ_210487 13029 RMVar_ID_13029 Human_SNP_ID_682730816 A-to-I Human chr20 - 47269087 47269087 47269087 TTAAGCAGTTCTCTTGCCTCAGCCCCCCAAGTAGCTGGGATTACAGGCATGTGCCAACACACCTG TTAAGCAGTTCTCTTGCCTCAGCCCCCCAAGTGGCTGGGATTACAGGCATGTGCCAACACACCTG T C ZMYND8 Ensembl:ENSG00000101040 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs528416827 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210488,RMVar_hsa_circ_3666,RMVar_hsa_circ_73732,RMVar_hsa_circ_4641,RMVar_hsa_circ_117845,RMVar_hsa_circ_82182,RMVar_hsa_circ_210472,RMVar_hsa_circ_210473,RMVar_hsa_circ_300845,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_281763,RMVar_hsa_circ_62862,RMVar_hsa_circ_87810,RMVar_hsa_circ_210482,RMVar_hsa_circ_210484,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_270363,RMVar_hsa_circ_210492,RMVar_hsa_circ_77505,RMVar_hsa_circ_96252,RMVar_hsa_circ_210494,RMVar_hsa_circ_210495,RMVar_hsa_circ_210493,RMVar_hsa_circ_210490,RMVar_hsa_circ_210491,RMVar_hsa_circ_210489,RMVar_hsa_circ_210486,RMVar_hsa_circ_210487 13030 RMVar_ID_13030 Human_SNP_ID_682731028 A-to-I Human chr20 - 47270009 47270009 47270009 AAACTCTTGGGCTCAAACGATCTGCCTGCCTCAGCCTCCCAAAATGCTGGGATAATAGGCATGAG AAACTCTTGGGCTCAAACGATCTGCCTGCCTCTGCCTCCCAAAATGCTGGGATAATAGGCATGAG T A ZMYND8 Ensembl:ENSG00000101040 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs960666473 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210488,RMVar_hsa_circ_3666,RMVar_hsa_circ_73732,RMVar_hsa_circ_4641,RMVar_hsa_circ_117845,RMVar_hsa_circ_82182,RMVar_hsa_circ_210472,RMVar_hsa_circ_210473,RMVar_hsa_circ_300845,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_281763,RMVar_hsa_circ_62862,RMVar_hsa_circ_87810,RMVar_hsa_circ_210482,RMVar_hsa_circ_210484,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_270363,RMVar_hsa_circ_210492,RMVar_hsa_circ_77505,RMVar_hsa_circ_96252,RMVar_hsa_circ_210494,RMVar_hsa_circ_210495,RMVar_hsa_circ_210493,RMVar_hsa_circ_210490,RMVar_hsa_circ_210491,RMVar_hsa_circ_210489,RMVar_hsa_circ_210486,RMVar_hsa_circ_210487 13031 RMVar_ID_13031 Human_SNP_ID_682731061 A-to-I Human chr20 - 47270112 47270112 47270112 CTGCCTCAGCCTCCTGAGTAGCTAGGAGTACAAGTGTGCGCCACCACACCTAGCTATACACCTAG CTGCCTCAGCCTCCTGAGTAGCTAGGAGTACAGGTGTGCGCCACCACACCTAGCTATACACCTAG T C ZMYND8 Ensembl:ENSG00000101040 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs942306320 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210488,RMVar_hsa_circ_3666,RMVar_hsa_circ_73732,RMVar_hsa_circ_4641,RMVar_hsa_circ_117845,RMVar_hsa_circ_82182,RMVar_hsa_circ_210472,RMVar_hsa_circ_210473,RMVar_hsa_circ_300845,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_281763,RMVar_hsa_circ_62862,RMVar_hsa_circ_87810,RMVar_hsa_circ_210482,RMVar_hsa_circ_210484,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_270363,RMVar_hsa_circ_210492,RMVar_hsa_circ_77505,RMVar_hsa_circ_96252,RMVar_hsa_circ_210494,RMVar_hsa_circ_210495,RMVar_hsa_circ_210493,RMVar_hsa_circ_210490,RMVar_hsa_circ_210491,RMVar_hsa_circ_210489,RMVar_hsa_circ_210486,RMVar_hsa_circ_210487 13032 RMVar_ID_13032 Human_SNP_ID_682731114 A-to-I Human chr20 - 47270304 47270304 47270304 CAATGGTGCGATCTTGGCTCACTGTAAACTCTACCACCTGGGTTCAAGCGATTCTCCTGCCTCAG CAATGGTGCGATCTTGGCTCACTGTAAACTCTCCCACCTGGGTTCAAGCGATTCTCCTGCCTCAG T G ZMYND8 Ensembl:ENSG00000101040 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1415795486 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7006734 RMVar_hsa_circ_210488,RMVar_hsa_circ_3666,RMVar_hsa_circ_73732,RMVar_hsa_circ_4641,RMVar_hsa_circ_117845,RMVar_hsa_circ_82182,RMVar_hsa_circ_210472,RMVar_hsa_circ_210473,RMVar_hsa_circ_300845,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_281763,RMVar_hsa_circ_62862,RMVar_hsa_circ_87810,RMVar_hsa_circ_210482,RMVar_hsa_circ_210484,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_270363,RMVar_hsa_circ_210492,RMVar_hsa_circ_77505,RMVar_hsa_circ_96252,RMVar_hsa_circ_210494,RMVar_hsa_circ_210495,RMVar_hsa_circ_210493,RMVar_hsa_circ_210490,RMVar_hsa_circ_210491,RMVar_hsa_circ_210489,RMVar_hsa_circ_210486,RMVar_hsa_circ_210487 13033 RMVar_ID_13033 Human_SNP_ID_682732410 A-to-I Human chr20 - 47275287 47275287 47275287 GGGTTTCACCATGTTGGCCTGGCTGGTCTCGAACTCCTGACTTCAAGTGATCCACCCGCCTTGGG GGGTTTCACCATGTTGGCCTGGCTGGTCTCGATCTCCTGACTTCAAGTGATCCACCCGCCTTGGG T A ZMYND8 Ensembl:ENSG00000101040 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1164079756 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210488,RMVar_hsa_circ_3666,RMVar_hsa_circ_73732,RMVar_hsa_circ_4641,RMVar_hsa_circ_117845,RMVar_hsa_circ_82182,RMVar_hsa_circ_210472,RMVar_hsa_circ_210473,RMVar_hsa_circ_300845,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_281763,RMVar_hsa_circ_62862,RMVar_hsa_circ_87810,RMVar_hsa_circ_210482,RMVar_hsa_circ_210484,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_270363,RMVar_hsa_circ_210492,RMVar_hsa_circ_77505,RMVar_hsa_circ_96252,RMVar_hsa_circ_210494,RMVar_hsa_circ_210495,RMVar_hsa_circ_210493,RMVar_hsa_circ_210490,RMVar_hsa_circ_210491,RMVar_hsa_circ_210489,RMVar_hsa_circ_210486,RMVar_hsa_circ_210487 13034 RMVar_ID_13034 Human_SNP_ID_682732421 A-to-I Human chr20 - 47275344 47275344 47275344 GATTACAGGTGCGCGCACTACTATGTCCAGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCA GATTACAGGTGCGCGCACTACTATGTCCAGCTGATTTTTGTATTTTTAGTAGAGACAGGGTTTCA T C ZMYND8 Ensembl:ENSG00000101040 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs964698036 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210488,RMVar_hsa_circ_3666,RMVar_hsa_circ_73732,RMVar_hsa_circ_4641,RMVar_hsa_circ_117845,RMVar_hsa_circ_82182,RMVar_hsa_circ_210472,RMVar_hsa_circ_210473,RMVar_hsa_circ_300845,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_281763,RMVar_hsa_circ_62862,RMVar_hsa_circ_87810,RMVar_hsa_circ_210482,RMVar_hsa_circ_210484,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_270363,RMVar_hsa_circ_210492,RMVar_hsa_circ_77505,RMVar_hsa_circ_96252,RMVar_hsa_circ_210494,RMVar_hsa_circ_210495,RMVar_hsa_circ_210493,RMVar_hsa_circ_210490,RMVar_hsa_circ_210491,RMVar_hsa_circ_210489,RMVar_hsa_circ_210486,RMVar_hsa_circ_210487 13035 RMVar_ID_13035 Human_SNP_ID_682732508 A-to-I Human chr20 - 47275671 47275671 47275671 CGGAGCCTGGGAGGTTGAGGCTGCAGTGAGCTATGATTGCGCTGTTGTATTCCAGCCTGGGCAAA CGGAGCCTGGGAGGTTGAGGCTGCAGTGAGCTCTGATTGCGCTGTTGTATTCCAGCCTGGGCAAA T G ZMYND8 Ensembl:ENSG00000101040 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1368292021 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14122670,Human_RBP_ID_17571661 RMVar_hsa_circ_210488,RMVar_hsa_circ_3666,RMVar_hsa_circ_73732,RMVar_hsa_circ_4641,RMVar_hsa_circ_117845,RMVar_hsa_circ_82182,RMVar_hsa_circ_210472,RMVar_hsa_circ_210473,RMVar_hsa_circ_300845,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_281763,RMVar_hsa_circ_62862,RMVar_hsa_circ_87810,RMVar_hsa_circ_210482,RMVar_hsa_circ_210484,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_270363,RMVar_hsa_circ_210492,RMVar_hsa_circ_77505,RMVar_hsa_circ_96252,RMVar_hsa_circ_210494,RMVar_hsa_circ_210495,RMVar_hsa_circ_210493,RMVar_hsa_circ_210490,RMVar_hsa_circ_210491,RMVar_hsa_circ_210489,RMVar_hsa_circ_210486,RMVar_hsa_circ_210487 13036 RMVar_ID_13036 Human_SNP_ID_682733467 A-to-I Human chr20 - 47279322 47279322 47279322 GGTATTACAGGGGCGTGCCACCACATCCGGCTAATTTTTCCATTTTTAGTAGAGATGGGGTTTCA GGTATTACAGGGGCGTGCCACCACATCCGGCTGATTTTTCCATTTTTAGTAGAGATGGGGTTTCA T C ZMYND8 Ensembl:ENSG00000101040 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1211385589 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 13037 RMVar_ID_13037 Human_SNP_ID_682735787 A-to-I Human chr20 - 47288668 47288668 47288668 AATGTGTGGGTCAGGTGCAGTGGCTCATGCCTATAATCACAGCACTTTGGGAAGCTGAGGCGGGC AATGTGTGGGTCAGGTGCAGTGGCTCATGCCTGTAATCACAGCACTTTGGGAAGCTGAGGCGGGC T C ZMYND8 Ensembl:ENSG00000101040 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs540834398 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571662 RMVar_hsa_circ_210488,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_278493,RMVar_hsa_circ_291951,RMVar_hsa_circ_333651,RMVar_hsa_circ_210482,RMVar_hsa_circ_12782,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_294255,RMVar_hsa_circ_77505,RMVar_hsa_circ_96252,RMVar_hsa_circ_210490,RMVar_hsa_circ_210489,RMVar_hsa_circ_10625,RMVar_hsa_circ_27851,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_279185,RMVar_hsa_circ_283317,RMVar_hsa_circ_22267,RMVar_hsa_circ_282534,RMVar_hsa_circ_210497,RMVar_hsa_circ_362029,RMVar_hsa_circ_295005,RMVar_hsa_circ_310420,RMVar_hsa_circ_270665,RMVar_hsa_circ_275363,RMVar_hsa_circ_41957,RMVar_hsa_circ_44135,RMVar_hsa_circ_210503,RMVar_hsa_circ_210505,RMVar_hsa_circ_210506,RMVar_hsa_circ_210504,RMVar_hsa_circ_332061,RMVar_hsa_circ_345744,RMVar_hsa_circ_340401,RMVar_hsa_circ_277990,RMVar_hsa_circ_210507,RMVar_hsa_circ_210508,RMVar_hsa_circ_210509,RMVar_hsa_circ_210511,RMVar_hsa_circ_65294,RMVar_hsa_circ_292254,RMVar_hsa_circ_294831,RMVar_hsa_circ_343228,RMVar_hsa_circ_292729,RMVar_hsa_circ_275908,RMVar_hsa_circ_16268,RMVar_hsa_circ_31833,RMVar_hsa_circ_210513,RMVar_hsa_circ_210514,RMVar_hsa_circ_210512 13038 RMVar_ID_13038 Human_SNP_ID_682735883 A-to-I Human chr20 - 47289045 47289045 47289045 CAGGCTGGACTGCAGTGGTGTGATCTCAGCTCACTGAAACCTCTGCCTCCTGGGTTGAAGCGATT CAGGCTGGACTGCAGTGGTGTGATCTCAGCTCCCTGAAACCTCTGCCTCCTGGGTTGAAGCGATT T G ZMYND8 Ensembl:ENSG00000101040 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1196056779 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210488,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_278493,RMVar_hsa_circ_291951,RMVar_hsa_circ_333651,RMVar_hsa_circ_210482,RMVar_hsa_circ_12782,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_294255,RMVar_hsa_circ_77505,RMVar_hsa_circ_96252,RMVar_hsa_circ_210490,RMVar_hsa_circ_210489,RMVar_hsa_circ_10625,RMVar_hsa_circ_27851,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_279185,RMVar_hsa_circ_283317,RMVar_hsa_circ_22267,RMVar_hsa_circ_282534,RMVar_hsa_circ_210497,RMVar_hsa_circ_362029,RMVar_hsa_circ_295005,RMVar_hsa_circ_310420,RMVar_hsa_circ_270665,RMVar_hsa_circ_275363,RMVar_hsa_circ_41957,RMVar_hsa_circ_44135,RMVar_hsa_circ_210503,RMVar_hsa_circ_210505,RMVar_hsa_circ_210506,RMVar_hsa_circ_210504,RMVar_hsa_circ_332061,RMVar_hsa_circ_345744,RMVar_hsa_circ_340401,RMVar_hsa_circ_277990,RMVar_hsa_circ_210507,RMVar_hsa_circ_210508,RMVar_hsa_circ_210509,RMVar_hsa_circ_210511,RMVar_hsa_circ_65294,RMVar_hsa_circ_292254,RMVar_hsa_circ_294831,RMVar_hsa_circ_343228,RMVar_hsa_circ_292729,RMVar_hsa_circ_275908,RMVar_hsa_circ_16268,RMVar_hsa_circ_31833,RMVar_hsa_circ_210513,RMVar_hsa_circ_210514,RMVar_hsa_circ_210512 13039 RMVar_ID_13039 Human_SNP_ID_682738137 A-to-I Human chr20 - 47297643 47297643 47297643 AGGCAGGAGAATTGCTTGATCCCAGGAGTTCAAGACCTGTCTGGGCAACATAGGGAGACCCCCAT AGGCAGGAGAATTGCTTGATCCCAGGAGTTCAGGACCTGTCTGGGCAACATAGGGAGACCCCCAT T C ZMYND8 Ensembl:ENSG00000101040 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264870308 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73732,RMVar_hsa_circ_117845,RMVar_hsa_circ_210472,RMVar_hsa_circ_55827,RMVar_hsa_circ_278493,RMVar_hsa_circ_12782,RMVar_hsa_circ_344781,RMVar_hsa_circ_210481,RMVar_hsa_circ_345800,RMVar_hsa_circ_317169,RMVar_hsa_circ_294255,RMVar_hsa_circ_77505,RMVar_hsa_circ_25000,RMVar_hsa_circ_27851,RMVar_hsa_circ_210486,RMVar_hsa_circ_210487,RMVar_hsa_circ_324384,RMVar_hsa_circ_307901,RMVar_hsa_circ_283317,RMVar_hsa_circ_282534,RMVar_hsa_circ_362029,RMVar_hsa_circ_310420,RMVar_hsa_circ_270665,RMVar_hsa_circ_41957,RMVar_hsa_circ_44135,RMVar_hsa_circ_210505,RMVar_hsa_circ_210506,RMVar_hsa_circ_332061,RMVar_hsa_circ_345744,RMVar_hsa_circ_210509,RMVar_hsa_circ_210511,RMVar_hsa_circ_65294,RMVar_hsa_circ_294831,RMVar_hsa_circ_275908,RMVar_hsa_circ_16268,RMVar_hsa_circ_31833,RMVar_hsa_circ_210512,RMVar_hsa_circ_30845,RMVar_hsa_circ_276234,RMVar_hsa_circ_291207,RMVar_hsa_circ_318101,RMVar_hsa_circ_47649,RMVar_hsa_circ_210517,RMVar_hsa_circ_210518,RMVar_hsa_circ_266201,RMVar_hsa_circ_292581,RMVar_hsa_circ_54299,RMVar_hsa_circ_210522,RMVar_hsa_circ_210520,RMVar_hsa_circ_279216,RMVar_hsa_circ_279977,RMVar_hsa_circ_210523,RMVar_hsa_circ_210521 13040 RMVar_ID_13040 Human_SNP_ID_682739298 A-to-I Human chr20 - 47302320 47302320 47302320 CAGGCATGTGCCACCATGCCCAGCTAATTTTTATATTTTTTGTAGAGATGGAGTTTCACCATGTT CAGGCATGTGCCACCATGCCCAGCTAATTTTTTTATTTTTTGTAGAGATGGAGTTTCACCATGTT T A ZMYND8 Ensembl:ENSG00000101040 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1312052194 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73732,RMVar_hsa_circ_117845,RMVar_hsa_circ_210472,RMVar_hsa_circ_55827,RMVar_hsa_circ_278493,RMVar_hsa_circ_12782,RMVar_hsa_circ_210481,RMVar_hsa_circ_345800,RMVar_hsa_circ_317169,RMVar_hsa_circ_77505,RMVar_hsa_circ_25000,RMVar_hsa_circ_27851,RMVar_hsa_circ_210486,RMVar_hsa_circ_210487,RMVar_hsa_circ_324384,RMVar_hsa_circ_283317,RMVar_hsa_circ_310420,RMVar_hsa_circ_270665,RMVar_hsa_circ_41957,RMVar_hsa_circ_44135,RMVar_hsa_circ_210506,RMVar_hsa_circ_65294,RMVar_hsa_circ_16268,RMVar_hsa_circ_31833,RMVar_hsa_circ_30845,RMVar_hsa_circ_318101,RMVar_hsa_circ_47649,RMVar_hsa_circ_54299,RMVar_hsa_circ_210524,RMVar_hsa_circ_345590,RMVar_hsa_circ_276545 13041 RMVar_ID_13041 Human_SNP_ID_682740193 A-to-I Human chr20 - 47305492 47305492 47305492 TCATGCCTGTAATCCTAGCACTTTGGGAGGCTAAGGTGGGCAGATCACCTGAGGCCAGGAGTTCG TCATGCCTGTAATCCTAGCACTTTGGGAGGCTCAGGTGGGCAGATCACCTGAGGCCAGGAGTTCG T G ZMYND8 Ensembl:ENSG00000101040 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs996183536 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73732,RMVar_hsa_circ_117845,RMVar_hsa_circ_210472,RMVar_hsa_circ_55827,RMVar_hsa_circ_278493,RMVar_hsa_circ_12782,RMVar_hsa_circ_210481,RMVar_hsa_circ_345800,RMVar_hsa_circ_317169,RMVar_hsa_circ_77505,RMVar_hsa_circ_25000,RMVar_hsa_circ_27851,RMVar_hsa_circ_210486,RMVar_hsa_circ_210487,RMVar_hsa_circ_324384,RMVar_hsa_circ_283317,RMVar_hsa_circ_310420,RMVar_hsa_circ_270665,RMVar_hsa_circ_41957,RMVar_hsa_circ_44135,RMVar_hsa_circ_210506,RMVar_hsa_circ_65294,RMVar_hsa_circ_16268,RMVar_hsa_circ_31833,RMVar_hsa_circ_30845,RMVar_hsa_circ_318101,RMVar_hsa_circ_47649,RMVar_hsa_circ_54299,RMVar_hsa_circ_210524,RMVar_hsa_circ_345590,RMVar_hsa_circ_276545 13042 RMVar_ID_13042 Human_SNP_ID_682746152 A-to-I Human chr20 - 47327534 47327534 47327534 CTCCTGCCTCAGCCTCCCAAGTAGCTGGAACTACAGGTGTGTGCCACCACGCCTGGCTAATATTT CTCCTGCCTCAGCCTCCCAAGTAGCTGGAACTTCAGGTGTGTGCCACCACGCCTGGCTAATATTT T A ZMYND8 Ensembl:ENSG00000101040 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1569207425 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22722953 RMVar_hsa_circ_73732,RMVar_hsa_circ_117845,RMVar_hsa_circ_210472,RMVar_hsa_circ_55827,RMVar_hsa_circ_278493,RMVar_hsa_circ_12782,RMVar_hsa_circ_210481,RMVar_hsa_circ_317169,RMVar_hsa_circ_77505,RMVar_hsa_circ_27851,RMVar_hsa_circ_210486,RMVar_hsa_circ_283317,RMVar_hsa_circ_270665,RMVar_hsa_circ_41957,RMVar_hsa_circ_44135,RMVar_hsa_circ_65294,RMVar_hsa_circ_31833,RMVar_hsa_circ_30845,RMVar_hsa_circ_318101,RMVar_hsa_circ_54299,RMVar_hsa_circ_210524,RMVar_hsa_circ_345590,RMVar_hsa_circ_293525 13043 RMVar_ID_13043 Human_SNP_ID_682749352 A-to-I Human chr20 - 47340169 47340169 47340169 GCCAAGCACTTTGAGAGGCGGATCATGAGGTCAGGAGTTTGAGACCAGCCTGGCCAATATGGTGA GCCAAGCACTTTGAGAGGCGGATCATGAGGTCCGGAGTTTGAGACCAGCCTGGCCAATATGGTGA T G ZMYND8 Ensembl:ENSG00000101040 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs905067405 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14123315,Human_RBP_ID_17571668 RMVar_hsa_circ_73732,RMVar_hsa_circ_117845,RMVar_hsa_circ_210472,RMVar_hsa_circ_55827,RMVar_hsa_circ_278493,RMVar_hsa_circ_12782,RMVar_hsa_circ_210481,RMVar_hsa_circ_317169,RMVar_hsa_circ_77505,RMVar_hsa_circ_27851,RMVar_hsa_circ_210486,RMVar_hsa_circ_283317,RMVar_hsa_circ_270665,RMVar_hsa_circ_41957,RMVar_hsa_circ_44135,RMVar_hsa_circ_65294,RMVar_hsa_circ_31833,RMVar_hsa_circ_30845,RMVar_hsa_circ_318101,RMVar_hsa_circ_54299,RMVar_hsa_circ_210524,RMVar_hsa_circ_345590,RMVar_hsa_circ_293525 13044 RMVar_ID_13044 Human_SNP_ID_682749465 A-to-I Human chr20 - 47340628 47340628 47340628 CGCCACACCCAGCTAATTTTTTAATTTTTAGTAGAGATGGGTTTTCACCATGTTGGCCAGGCTGG CGCCACACCCAGCTAATTTTTTAATTTTTAGTGGAGATGGGTTTTCACCATGTTGGCCAGGCTGG T C ZMYND8 Ensembl:ENSG00000101040 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913989378 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73732,RMVar_hsa_circ_117845,RMVar_hsa_circ_210472,RMVar_hsa_circ_55827,RMVar_hsa_circ_278493,RMVar_hsa_circ_12782,RMVar_hsa_circ_210481,RMVar_hsa_circ_317169,RMVar_hsa_circ_77505,RMVar_hsa_circ_27851,RMVar_hsa_circ_210486,RMVar_hsa_circ_283317,RMVar_hsa_circ_270665,RMVar_hsa_circ_41957,RMVar_hsa_circ_44135,RMVar_hsa_circ_65294,RMVar_hsa_circ_31833,RMVar_hsa_circ_30845,RMVar_hsa_circ_318101,RMVar_hsa_circ_54299,RMVar_hsa_circ_210524,RMVar_hsa_circ_345590,RMVar_hsa_circ_293525 13045 RMVar_ID_13045 Human_SNP_ID_682749486 A-to-I Human chr20 - 47340705 47340705 47340705 TTGGCTCGCTGCAACCTTCATTTCCCGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCTGAGTAGC TTGGCTCGCTGCAACCTTCATTTCCCGGGTTCCAGTGATTCTCCTGCCTCAGCCTCCTGAGTAGC T G ZMYND8 Ensembl:ENSG00000101040 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1269789142 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73732,RMVar_hsa_circ_117845,RMVar_hsa_circ_210472,RMVar_hsa_circ_55827,RMVar_hsa_circ_278493,RMVar_hsa_circ_12782,RMVar_hsa_circ_210481,RMVar_hsa_circ_317169,RMVar_hsa_circ_77505,RMVar_hsa_circ_27851,RMVar_hsa_circ_210486,RMVar_hsa_circ_283317,RMVar_hsa_circ_270665,RMVar_hsa_circ_41957,RMVar_hsa_circ_44135,RMVar_hsa_circ_65294,RMVar_hsa_circ_31833,RMVar_hsa_circ_30845,RMVar_hsa_circ_318101,RMVar_hsa_circ_54299,RMVar_hsa_circ_210524,RMVar_hsa_circ_345590,RMVar_hsa_circ_293525 13046 RMVar_ID_13046 Human_SNP_ID_682750186 A-to-I Human chr20 - 47343161 47343161 47343161 CTTGCCTCAGCCTCCCAAGTAGCTGGGACCACAGGCATGCATCACCACAGTTGGCTAATTTTTGT CTTGCCTCAGCCTCCCAAGTAGCTGGGACCACTGGCATGCATCACCACAGTTGGCTAATTTTTGT T A ZMYND8 Ensembl:ENSG00000101040 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1341142957 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73732,RMVar_hsa_circ_117845,RMVar_hsa_circ_210472,RMVar_hsa_circ_55827,RMVar_hsa_circ_278493,RMVar_hsa_circ_12782,RMVar_hsa_circ_210481,RMVar_hsa_circ_317169,RMVar_hsa_circ_77505,RMVar_hsa_circ_27851,RMVar_hsa_circ_210486,RMVar_hsa_circ_283317,RMVar_hsa_circ_270665,RMVar_hsa_circ_41957,RMVar_hsa_circ_44135,RMVar_hsa_circ_65294,RMVar_hsa_circ_31833,RMVar_hsa_circ_30845,RMVar_hsa_circ_318101,RMVar_hsa_circ_54299,RMVar_hsa_circ_210524,RMVar_hsa_circ_345590,RMVar_hsa_circ_293525 13047 RMVar_ID_13047 Human_SNP_ID_682750298 A-to-I Human chr20 - 47343700 47343700 47343700 TTGAGGCCAGGAGTTCGAGACCAGCCTGGCCAACGTGGCAAAATCCCATCTCTACTAAAAATAAC TTGAGGCCAGGAGTTCGAGACCAGCCTGGCCAGCGTGGCAAAATCCCATCTCTACTAAAAATAAC T C ZMYND8 Ensembl:ENSG00000101040 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1450127683 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73732,RMVar_hsa_circ_117845,RMVar_hsa_circ_210472,RMVar_hsa_circ_55827,RMVar_hsa_circ_278493,RMVar_hsa_circ_12782,RMVar_hsa_circ_210481,RMVar_hsa_circ_317169,RMVar_hsa_circ_77505,RMVar_hsa_circ_27851,RMVar_hsa_circ_210486,RMVar_hsa_circ_283317,RMVar_hsa_circ_270665,RMVar_hsa_circ_41957,RMVar_hsa_circ_44135,RMVar_hsa_circ_65294,RMVar_hsa_circ_31833,RMVar_hsa_circ_30845,RMVar_hsa_circ_318101,RMVar_hsa_circ_54299,RMVar_hsa_circ_210524,RMVar_hsa_circ_345590,RMVar_hsa_circ_293525 13048 RMVar_ID_13048 Human_SNP_ID_682767018 A-to-I Human chr20 - 47407746 47407746 47407746 TACCACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGAC TACCACCATGCCTGGCTAATTTTTGTATTTTTGGTAGAGATGGGGTTTCACCATGTTGGCCAGAC T C LINC01754 Ensembl:ENSG00000224565 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs747662520 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49223 13049 RMVar_ID_13049 Human_SNP_ID_682767621 A-to-I Human chr20 - 47409936 47409936 47409936 AAACCCCATCTCTACTAAAAATAACAAAAATTAGCTGGGCATGGTGGTGCATGTCTGTAATTCCA AAACCCCATCTCTACTAAAAATAACAAAAATTGGCTGGGCATGGTGGTGCATGTCTGTAATTCCA T C LINC01754 Ensembl:ENSG00000224565 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1243336295 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49223 13050 RMVar_ID_13050 Human_SNP_ID_682767911 A-to-I Human chr20 - 47411043 47411043 47411043 CTGTCGCCCAGGCTGAAGTGCAGTGGCATGATATCAGCTCACTGCAACCTCTGCCTCCGAGGTTC CTGTCGCCCAGGCTGAAGTGCAGTGGCATGATCTCAGCTCACTGCAACCTCTGCCTCCGAGGTTC T G LINC01754 Ensembl:ENSG00000224565 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1166237142 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49223 13051 RMVar_ID_13051 Human_SNP_ID_682792247 A-to-I Human chr20 + 47504593 47504593 47504593 TTGGGAAGCCAAGGCTGGTGGATCACGAGGTCAGGAGTTTGAGAACAGCCTGGCAAAGATGGTGA TTGGGAAGCCAAGGCTGGTGGATCACGAGGTCGGGAGTTTGAGAACAGCCTGGCAAAGATGGTGA A G NCOA3 Ensembl:ENSG00000124151 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1204994740 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210526,RMVar_hsa_circ_95052 13052 RMVar_ID_13052 Human_SNP_ID_682793417 A-to-I Human chr20 + 47509128 47509128 47509128 CTGACTTATAAAGAATTTAGAGGCTGGGTCCCATGGCTCACACCTGTAATCCCAGCACTTTGAGA CTGACTTATAAAGAATTTAGAGGCTGGGTCCCGTGGCTCACACCTGTAATCCCAGCACTTTGAGA A G NCOA3 Ensembl:ENSG00000124151 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1020387101 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14123659,Human_RBP_ID_23907925 RMVar_hsa_circ_210526,RMVar_hsa_circ_95052 13053 RMVar_ID_13053 Human_SNP_ID_682793423 A-to-I Human chr20 + 47509169 47509169 47509169 ACCTGTAATCCCAGCACTTTGAGAGGAGGATCACTTGAGCCCAGGAATTTGAGACCAGCCTGGGC ACCTGTAATCCCAGCACTTTGAGAGGAGGATCGCTTGAGCCCAGGAATTTGAGACCAGCCTGGGC A G NCOA3 Ensembl:ENSG00000124151 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs771694701 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210526,RMVar_hsa_circ_95052 13054 RMVar_ID_13054 Human_SNP_ID_682793545 A-to-I Human chr20 + 47509658 47509657 47509658 GGCTGAGTGCAGTGGCTCCTGCCTGTAATCCCAGCAATTTGGGAGGCTGAGACCAGAGACTTGCT GGCTGAGTGCAGTGGCTCCTGCCTGTAATCCC_GCAATTTGGGAGGCTGAGACCAGAGACTTGCT CA C NCOA3 Ensembl:ENSG00000124151 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1556555457 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_17143077 RMVar_hsa_circ_210526,RMVar_hsa_circ_95052 13055 RMVar_ID_13055 Human_SNP_ID_682793546 A-to-I Human chr20 + 47509658 47509658 47509658 GGCTGAGTGCAGTGGCTCCTGCCTGTAATCCCAGCAATTTGGGAGGCTGAGACCAGAGACTTGCT GGCTGAGTGCAGTGGCTCCTGCCTGTAATCCCGGCAATTTGGGAGGCTGAGACCAGAGACTTGCT A G NCOA3 Ensembl:ENSG00000124151 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6012196 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17143077 RMVar_hsa_circ_210526,RMVar_hsa_circ_95052 13056 RMVar_ID_13056 Human_SNP_ID_682793550 A-to-I Human chr20 + 47509677 47509677 47509677 TGCCTGTAATCCCAGCAATTTGGGAGGCTGAGACCAGAGACTTGCTTGAGCCTAGGAGTTCAAGA TGCCTGTAATCCCAGCAATTTGGGAGGCTGAGGCCAGAGACTTGCTTGAGCCTAGGAGTTCAAGA A G NCOA3 Ensembl:ENSG00000124151 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6012197 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210526,RMVar_hsa_circ_95052 13057 RMVar_ID_13057 Human_SNP_ID_682793834 A-to-I Human chr20 + 47510740 47510740 47510740 CGCAGCCTCCCAGTAGCTGTGACTACAGGCACATGTCACCACTCCTGGCTGATGTTTTTAAGTTT CGCAGCCTCCCAGTAGCTGTGACTACAGGCACGTGTCACCACTCCTGGCTGATGTTTTTAAGTTT A G NCOA3 Ensembl:ENSG00000124151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1359994475 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210526,RMVar_hsa_circ_95052 13058 RMVar_ID_13058 Human_SNP_ID_682794227 A-to-I Human chr20 + 47511599 47511599 47511599 TTTTGAGACGGTCTTGCTCTGTCACCCAGGCTAGAATGCACTGGTGCTATCTCAGATCACCGCAA TTTTGAGACGGTCTTGCTCTGTCACCCAGGCTGGAATGCACTGGTGCTATCTCAGATCACCGCAA A G NCOA3 Ensembl:ENSG00000124151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1430331873 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14123674 RMVar_hsa_circ_210526,RMVar_hsa_circ_95052 13059 RMVar_ID_13059 Human_SNP_ID_682794249 A-to-I Human chr20 + 47511690 47511690 47511690 CTCCTGCCTCAGCCACCCGAGTAGCTGGGGTTACAGGCAGCACTACCACGTGGACCCAGCTAATT CTCCTGCCTCAGCCACCCGAGTAGCTGGGGTTGCAGGCAGCACTACCACGTGGACCCAGCTAATT A G NCOA3 Ensembl:ENSG00000124151 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1004514389 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210526,RMVar_hsa_circ_95052 13060 RMVar_ID_13060 Human_SNP_ID_682794263 A-to-I Human chr20 + 47511751 47511751 47511751 AATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCTTGTTGGCCAGGCTGATCTTGAACTCCTGG AATTTTTGTATTTTTAGTAGAGACGGGGTTTCTCCTTGTTGGCCAGGCTGATCTTGAACTCCTGG A T NCOA3 Ensembl:ENSG00000124151 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1030415726 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210526,RMVar_hsa_circ_95052 13061 RMVar_ID_13061 Human_SNP_ID_682794455 A-to-I Human chr20 + 47512457 47512457 47512457 GGGCATGGTGGCACATGCCTGTAGTCCCAGCTACTCGGGAGGTTGAGGCAGGAGAATTGCTTGAA GGGCATGGTGGCACATGCCTGTAGTCCCAGCTCCTCGGGAGGTTGAGGCAGGAGAATTGCTTGAA A C NCOA3 Ensembl:ENSG00000124151 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs574735277 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210526,RMVar_hsa_circ_95052 13062 RMVar_ID_13062 Human_SNP_ID_682794456 A-to-I Human chr20 + 47512457 47512457 47512457 GGGCATGGTGGCACATGCCTGTAGTCCCAGCTACTCGGGAGGTTGAGGCAGGAGAATTGCTTGAA GGGCATGGTGGCACATGCCTGTAGTCCCAGCTGCTCGGGAGGTTGAGGCAGGAGAATTGCTTGAA A G NCOA3 Ensembl:ENSG00000124151 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs574735277 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210526,RMVar_hsa_circ_95052 13063 RMVar_ID_13063 Human_SNP_ID_682794621 A-to-I Human chr20 + 47513011 47513011 47513011 AAACCTGGTCTCTACTAAAAATACAAAAAATTAGCCAGATGTGATGGTGTGTGCCTGTAACCCCA AAACCTGGTCTCTACTAAAAATACAAAAAATTGGCCAGATGTGATGGTGTGTGCCTGTAACCCCA A G NCOA3 Ensembl:ENSG00000124151 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs748877430 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210526,RMVar_hsa_circ_95052 13064 RMVar_ID_13064 Human_SNP_ID_682794730 A-to-I Human chr20 + 47513547 47513547 47513547 CAGGAGTTTGAGACCAGCCTGGCCAACATGGCAAAATGCGGTTTCTACTAAAAATACAAAAATTA CAGGAGTTTGAGACCAGCCTGGCCAACATGGCGAAATGCGGTTTCTACTAAAAATACAAAAATTA A G NCOA3 Ensembl:ENSG00000124151 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1367916643 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210526,RMVar_hsa_circ_95052 13065 RMVar_ID_13065 Human_SNP_ID_682795096 A-to-I Human chr20 + 47514868 47514868 47514868 CACTATGCCTGGCTAATTTTTGTATTTTTAGCAGAGACAGAGTTTTGCCATGTTGGCCAGGCTGG CACTATGCCTGGCTAATTTTTGTATTTTTAGCGGAGACAGAGTTTTGCCATGTTGGCCAGGCTGG A G NCOA3 Ensembl:ENSG00000124151 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs933520533 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210526,RMVar_hsa_circ_95052 13066 RMVar_ID_13066 Human_SNP_ID_682795195 A-to-I Human chr20 + 47515240 47515240 47515240 CCTGGAGTGCAGTGGCACGATCTCCGCTCACCACAACCTCCGCCTCCTGAGTTCAAACAATTCTC CCTGGAGTGCAGTGGCACGATCTCCGCTCACCCCAACCTCCGCCTCCTGAGTTCAAACAATTCTC A C NCOA3 Ensembl:ENSG00000124151 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1055206534 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210526,RMVar_hsa_circ_95052 13067 RMVar_ID_13067 Human_SNP_ID_682795196 A-to-I Human chr20 + 47515240 47515240 47515240 CCTGGAGTGCAGTGGCACGATCTCCGCTCACCACAACCTCCGCCTCCTGAGTTCAAACAATTCTC CCTGGAGTGCAGTGGCACGATCTCCGCTCACCGCAACCTCCGCCTCCTGAGTTCAAACAATTCTC A G NCOA3 Ensembl:ENSG00000124151 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1055206534 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210526,RMVar_hsa_circ_95052 13068 RMVar_ID_13068 Human_SNP_ID_682795327 A-to-I Human chr20 + 47515584 47515584 47515584 TCTCGGCTCACTGCAGTCTGCCTTCTGGGTTTAAGCGATTCTTATGCCTCAGCGTACTGAGTAGC TCTCGGCTCACTGCAGTCTGCCTTCTGGGTTTGAGCGATTCTTATGCCTCAGCGTACTGAGTAGC A G NCOA3 Ensembl:ENSG00000124151 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs189666808 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210526,RMVar_hsa_circ_95052 13069 RMVar_ID_13069 Human_SNP_ID_682795351 A-to-I Human chr20 + 47515665 47515665 47515665 CACCACCACTCCCAGCTAATTTTTTATTTTTTAGTAGAGACGGGATTTCACTATGTTGGCTGGTC CACCACCACTCCCAGCTAATTTTTTATTTTTTGGTAGAGACGGGATTTCACTATGTTGGCTGGTC A G NCOA3 Ensembl:ENSG00000124151 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs578067236 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210526,RMVar_hsa_circ_95052 13070 RMVar_ID_13070 Human_SNP_ID_682795374 A-to-I Human chr20 + 47515748 47515748 47515748 GTGGTCCGCCCACCTCAGCTTCCCAATGTGTTAGGATTACAGGCGTGAGCCACTGCCCTCAGCCT GTGGTCCGCCCACCTCAGCTTCCCAATGTGTTCGGATTACAGGCGTGAGCCACTGCCCTCAGCCT A C NCOA3 Ensembl:ENSG00000124151 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7262254 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210526,RMVar_hsa_circ_95052 13071 RMVar_ID_13071 Human_SNP_ID_682795376 A-to-I Human chr20 + 47515754 47515754 47515754 CGCCCACCTCAGCTTCCCAATGTGTTAGGATTACAGGCGTGAGCCACTGCCCTCAGCCTTAATAC CGCCCACCTCAGCTTCCCAATGTGTTAGGATTCCAGGCGTGAGCCACTGCCCTCAGCCTTAATAC A C NCOA3 Ensembl:ENSG00000124151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1159783157 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210526,RMVar_hsa_circ_95052 13072 RMVar_ID_13072 Human_SNP_ID_682795651 A-to-I Human chr20 + 47516965 47516965 47516965 AAAAAATTTGCTGGGTGCAGTGACTCACATCTATAATCCCAGCACTTTGAGAGGCCTAGACGGAT AAAAAATTTGCTGGGTGCAGTGACTCACATCTGTAATCCCAGCACTTTGAGAGGCCTAGACGGAT A G NCOA3 Ensembl:ENSG00000124151 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs924300938 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210526,RMVar_hsa_circ_95052 13073 RMVar_ID_13073 Human_SNP_ID_682795834 A-to-I Human chr20 + 47517577 47517577 47517577 GGTTCAAGTGATTCTCCTGCCTCAGCCTCCCTAGTAGCTGGGATTACAGGTGCTCGCTACTACAC GGTTCAAGTGATTCTCCTGCCTCAGCCTCCCTGGTAGCTGGGATTACAGGTGCTCGCTACTACAC A G NCOA3 Ensembl:ENSG00000124151 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1264130321 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210526,RMVar_hsa_circ_95052 13074 RMVar_ID_13074 Human_SNP_ID_682795846 A-to-I Human chr20 + 47517631 47517631 47517631 CGCTACTACACCTGGCTAATTTTTGTATTTTTAGTAGAGACGGGTTTTTGCCATGTTGGCCAGGC CGCTACTACACCTGGCTAATTTTTGTATTTTTGGTAGAGACGGGTTTTTGCCATGTTGGCCAGGC A G NCOA3 Ensembl:ENSG00000124151 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1291345210 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210526,RMVar_hsa_circ_95052 13075 RMVar_ID_13075 Human_SNP_ID_682795984 A-to-I Human chr20 + 47518271 47518271 47518271 AGGAGACTGAGGTGGGAGGATCGCTTAAGTCCAGGAGTTCCAGGCTGCAATGAGCCATGATTTCA AGGAGACTGAGGTGGGAGGATCGCTTAAGTCCTGGAGTTCCAGGCTGCAATGAGCCATGATTTCA A T NCOA3 Ensembl:ENSG00000124151 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs530063463 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210526,RMVar_hsa_circ_95052 13076 RMVar_ID_13076 Human_SNP_ID_682796076 A-to-I Human chr20 + 47518605 47518605 47518605 GCACCACTAAGCCTGGCTACTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGTCAGGC GCACCACTAAGCCTGGCTACTTTTGTATTTTTGGTAGAGATGGGGTTTCACCATGTTGGTCAGGC A G NCOA3 Ensembl:ENSG00000124151 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs889322655 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210526,RMVar_hsa_circ_95052 13077 RMVar_ID_13077 Human_SNP_ID_682796167 A-to-I Human chr20 + 47518949 47518949 47518949 CTTGAGGTCAGGAGTTTGCAACCAACCTGGCCAACATGGTGAAACCTCATCTCTACTAAAAATAC CTTGAGGTCAGGAGTTTGCAACCAACCTGGCCGACATGGTGAAACCTCATCTCTACTAAAAATAC A G NCOA3 Ensembl:ENSG00000124151 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1043220793 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210526,RMVar_hsa_circ_95052 13078 RMVar_ID_13078 Human_SNP_ID_682796252 A-to-I Human chr20 + 47519233 47519218 47519234 GAGGCGGGTGGATCACTTGAGGTCAGAAGATCAAGACCACCCTGGCTAACATGGTGAAATGCTGT GAGGCGGGTGGATCACTT________________GACCACCCTGGCTAACATGGTGAAATGCTGT TGAGGTCAGAAGATCAA T NCOA3 Ensembl:ENSG00000124151 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1281983769 Functional Loss DEL dbSNP153 19..34 33 - - - RMVar_hsa_circ_210526,RMVar_hsa_circ_95052 13079 RMVar_ID_13079 Human_SNP_ID_682796408 A-to-I Human chr20 + 47519818 47519818 47519818 AGAGTCTCGCTGTGTTGCTCAAGCTGGAGTGCAATGGCACAATCTCGCTCACTGCAACCTCTGCC AGAGTCTCGCTGTGTTGCTCAAGCTGGAGTGCGATGGCACAATCTCGCTCACTGCAACCTCTGCC A G NCOA3 Ensembl:ENSG00000124151 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1294056722 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210526,RMVar_hsa_circ_95052 13080 RMVar_ID_13080 Human_SNP_ID_682796424 A-to-I Human chr20 + 47519891 47519891 47519891 TCAAGAGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTATATAGATGCCCACCACCACGCC TCAAGAGATTCTCCTGCCTCAGCCTCCCAAGTCGCTGGGACTATATAGATGCCCACCACCACGCC A C NCOA3 Ensembl:ENSG00000124151 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs998033127 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210526,RMVar_hsa_circ_95052 13081 RMVar_ID_13081 Human_SNP_ID_682796436 A-to-I Human chr20 + 47519944 47519944 47519944 CACCACCACGCCTGGCTAATATTTGTATTTTTAGTAGAACCGGGGTTTCACCATGTTGGTCAGGC CACCACCACGCCTGGCTAATATTTGTATTTTTGGTAGAACCGGGGTTTCACCATGTTGGTCAGGC A G NCOA3 Ensembl:ENSG00000124151 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1252806820 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210526,RMVar_hsa_circ_95052 13082 RMVar_ID_13082 Human_SNP_ID_682799687 A-to-I Human chr20 + 47530482 47530482 47530482 TAATGATTTAACTTTTTTTTTTTTTTTTTTTGAGACAGAGTCTTACTCTGTCACCCAGGCTGTAG TAATGATTTAACTTTTTTTTTTTTTTTTTTTGTGACAGAGTCTTACTCTGTCACCCAGGCTGTAG A T NCOA3 Ensembl:ENSG00000124151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1555800768 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14123786 RMVar_hsa_circ_210526,RMVar_hsa_circ_95052,RMVar_hsa_circ_210527 13083 RMVar_ID_13083 Human_SNP_ID_682799840 A-to-I Human chr20 + 47531137 47531137 47531137 AGGGCAGGCAGATCACTTGAGGTAAGGAGTTCAAGATCAGCCTGGCCAACGTGGTGAAGCCCTGT AGGGCAGGCAGATCACTTGAGGTAAGGAGTTCTAGATCAGCCTGGCCAACGTGGTGAAGCCCTGT A T NCOA3 Ensembl:ENSG00000124151 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs563590611 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25616175 RMVar_hsa_circ_210526,RMVar_hsa_circ_95052,RMVar_hsa_circ_210527 13084 RMVar_ID_13084 Human_SNP_ID_682800536 A-to-I Human chr20 + 47533778 47533778 47533778 TAGATCCTATCTCTACAAAAAATGCAGAAATTAGCCCAGCATGGTGGCAGGTGCCTGTGGTCCTA TAGATCCTATCTCTACAAAAAATGCAGAAATTTGCCCAGCATGGTGGCAGGTGCCTGTGGTCCTA A T NCOA3 Ensembl:ENSG00000124151 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1324126201 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210526,RMVar_hsa_circ_95052,RMVar_hsa_circ_210527 13085 RMVar_ID_13085 Human_SNP_ID_682800755 A-to-I Human chr20 + 47534690 47534690 47534690 TAACCCCAGCACTTTGGGAGGCTGAGGCAGGCAGATCACTTGAGCTTAGGAGTTCAAGAGCAGTC TAACCCCAGCACTTTGGGAGGCTGAGGCAGGCGGATCACTTGAGCTTAGGAGTTCAAGAGCAGTC A G NCOA3 Ensembl:ENSG00000124151 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1426362710 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210526,RMVar_hsa_circ_95052,RMVar_hsa_circ_210527 13086 RMVar_ID_13086 Human_SNP_ID_682800783 A-to-I Human chr20 + 47534795 47534795 47534795 AAAATTGTCTGGGTGTGGTGGCGTGCACCTGTAGTCCCAGCTGTTGGGTGGCTGAGGTGGGAGGA AAAATTGTCTGGGTGTGGTGGCGTGCACCTGTTGTCCCAGCTGTTGGGTGGCTGAGGTGGGAGGA A T NCOA3 Ensembl:ENSG00000124151 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs960496529 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571682 RMVar_hsa_circ_210526,RMVar_hsa_circ_95052,RMVar_hsa_circ_210527 13087 RMVar_ID_13087 Human_SNP_ID_682801628 A-to-I Human chr20 + 47537764 47537763 47537765 ACCACACCCGGCTAATTTTTTCTACTTTTAGTAGAGATTGGGTTTCACTGTGTTAGCCAGGATGG ACCACACCCGGCTAATTTTTTCTACTTTTAGT__AGATTGGGTTTCACTGTGTTAGCCAGGATGG TAG T NCOA3 Ensembl:ENSG00000124151 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1159675803 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_210526,RMVar_hsa_circ_95052,RMVar_hsa_circ_210527 13088 RMVar_ID_13088 Human_SNP_ID_682803040 A-to-I Human chr20 + 47542704 47542704 47542704 TAAAAATTGGCCAGGCATGGTGGCTCATGCCTATAGTCCCAGCGCTTTGGGAAGCCCAGGCGGGT TAAAAATTGGCCAGGCATGGTGGCTCATGCCTGTAGTCCCAGCGCTTTGGGAAGCCCAGGCGGGT A G NCOA3 Ensembl:ENSG00000124151 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1225005365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571688,Human_RBP_ID_25616199 RMVar_hsa_circ_210526,RMVar_hsa_circ_95052,RMVar_hsa_circ_210527 13089 RMVar_ID_13089 Human_SNP_ID_682814823 A-to-I Human chr20 + 47590790 47590790 47590790 CCGTGATCGCACCATCGCACCCCATCCTGGGCAAGAGACCAAGACCCTGCCTCAAAACAAAACAA CCGTGATCGCACCATCGCACCCCATCCTGGGCGAGAGACCAAGACCCTGCCTCAAAACAAAACAA A G NCOA3 Ensembl:ENSG00000124151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs765275044 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210526,RMVar_hsa_circ_95052,RMVar_hsa_circ_52365 13090 RMVar_ID_13090 Human_SNP_ID_683091484 A-to-I Human chr20 - 48648051 48648051 48648051 AAAAAATCCTAAAATTAGCCAGGCGTGATGGCATACACCTGTTGTCCCAGCTCCTCAGTGTGCTG AAAAAATCCTAAAATTAGCCAGGCGTGATGGCGTACACCTGTTGTCCCAGCTCCTCAGTGTGCTG T C PREX1 Ensembl:ENSG00000124126 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs919836393 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121864,RMVar_hsa_circ_85593,RMVar_hsa_circ_210552,RMVar_hsa_circ_210553,RMVar_hsa_circ_105009,RMVar_hsa_circ_70266,RMVar_hsa_circ_210554,RMVar_hsa_circ_123791,RMVar_hsa_circ_107290,RMVar_hsa_circ_210556,RMVar_hsa_circ_210557,RMVar_hsa_circ_267852 13091 RMVar_ID_13091 Human_SNP_ID_683091491 A-to-I Human chr20 - 48648067 48648067 48648067 CCCTATCTCTATAAAAAAAAAATCCTAAAATTAGCCAGGCGTGATGGCATACACCTGTTGTCCCA CCCTATCTCTATAAAAAAAAAATCCTAAAATTGGCCAGGCGTGATGGCATACACCTGTTGTCCCA T C PREX1 Ensembl:ENSG00000124126 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1047923507 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121864,RMVar_hsa_circ_85593,RMVar_hsa_circ_210552,RMVar_hsa_circ_210553,RMVar_hsa_circ_105009,RMVar_hsa_circ_70266,RMVar_hsa_circ_210554,RMVar_hsa_circ_123791,RMVar_hsa_circ_107290,RMVar_hsa_circ_210556,RMVar_hsa_circ_210557,RMVar_hsa_circ_267852 13092 RMVar_ID_13092 Human_SNP_ID_683091492 A-to-I Human chr20 - 48648067 48648067 48648067 CCCTATCTCTATAAAAAAAAAATCCTAAAATTAGCCAGGCGTGATGGCATACACCTGTTGTCCCA CCCTATCTCTATAAAAAAAAAATCCTAAAATTCGCCAGGCGTGATGGCATACACCTGTTGTCCCA T G PREX1 Ensembl:ENSG00000124126 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1047923507 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121864,RMVar_hsa_circ_85593,RMVar_hsa_circ_210552,RMVar_hsa_circ_210553,RMVar_hsa_circ_105009,RMVar_hsa_circ_70266,RMVar_hsa_circ_210554,RMVar_hsa_circ_123791,RMVar_hsa_circ_107290,RMVar_hsa_circ_210556,RMVar_hsa_circ_210557,RMVar_hsa_circ_267852 13093 RMVar_ID_13093 Human_SNP_ID_683161138 A-to-I Human chr20 + 48926598 48926598 48926598 CTCCCATTTCAGCCTCCCAAGTAGCTAGGACTACAGGGGCGTACCACCCACCTGGCTAATTTTTC CTCCCATTTCAGCCTCCCAAGTAGCTAGGACTGCAGGGGCGTACCACCCACCTGGCTAATTTTTC A G ARFGEF2 Ensembl:ENSG00000124198 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1015440276 Functional Loss SNV dbSNP153 33..33 33 - - - 13094 RMVar_ID_13094 Human_SNP_ID_683166385 A-to-I Human chr20 + 48946905 48946905 48946905 CTCACTGCAGCCTCAAACTCCTGGACTCATGTAATCCTCCCACCTCAGCCTCCCGAGTAGCTGGG CTCACTGCAGCCTCAAACTCCTGGACTCATGTGATCCTCCCACCTCAGCCTCCCGAGTAGCTGGG A G ARFGEF2 Ensembl:ENSG00000124198 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027183272 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39821,RMVar_hsa_circ_57380,RMVar_hsa_circ_317557,RMVar_hsa_circ_12076,RMVar_hsa_circ_5981,RMVar_hsa_circ_359,RMVar_hsa_circ_6503,RMVar_hsa_circ_66207,RMVar_hsa_circ_210576,RMVar_hsa_circ_309647,RMVar_hsa_circ_15654 13095 RMVar_ID_13095 Human_SNP_ID_683169703 A-to-I Human chr20 + 48959689 48959689 48959689 TGGAGTGCAGTGGCGCAATCTCAAATCACTGCAACCTCTGCCTCTCAGGCTCAAGTGATCCTCCT TGGAGTGCAGTGGCGCAATCTCAAATCACTGCGACCTCTGCCTCTCAGGCTCAAGTGATCCTCCT A G ARFGEF2 Ensembl:ENSG00000124198 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1052562077 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39821,RMVar_hsa_circ_57380,RMVar_hsa_circ_12076,RMVar_hsa_circ_90847,RMVar_hsa_circ_8994,RMVar_hsa_circ_70925,RMVar_hsa_circ_5981,RMVar_hsa_circ_359,RMVar_hsa_circ_6503,RMVar_hsa_circ_66207,RMVar_hsa_circ_15654,RMVar_hsa_circ_113756,RMVar_hsa_circ_295586,RMVar_hsa_circ_322148,RMVar_hsa_circ_349851,RMVar_hsa_circ_125828,RMVar_hsa_circ_91898,RMVar_hsa_circ_104358,RMVar_hsa_circ_90229,RMVar_hsa_circ_210579,RMVar_hsa_circ_210581,RMVar_hsa_circ_53966,RMVar_hsa_circ_210582,RMVar_hsa_circ_210580,RMVar_hsa_circ_210577,RMVar_hsa_circ_210578,RMVar_hsa_circ_293164,RMVar_hsa_circ_343126,RMVar_hsa_circ_306847,RMVar_hsa_circ_98203,RMVar_hsa_circ_279429,RMVar_hsa_circ_210589,RMVar_hsa_circ_210590,RMVar_hsa_circ_210588,RMVar_hsa_circ_335277,RMVar_hsa_circ_293716,RMVar_hsa_circ_119777,RMVar_hsa_circ_272368,RMVar_hsa_circ_100541,RMVar_hsa_circ_96615,RMVar_hsa_circ_97813,RMVar_hsa_circ_93684,RMVar_hsa_circ_210591,RMVar_hsa_circ_41333,RMVar_hsa_circ_81582,RMVar_hsa_circ_87170,RMVar_hsa_circ_76773,RMVar_hsa_circ_210595,RMVar_hsa_circ_210599,RMVar_hsa_circ_210601,RMVar_hsa_circ_210602,RMVar_hsa_circ_210603,RMVar_hsa_circ_210600,RMVar_hsa_circ_210597,RMVar_hsa_circ_210598,RMVar_hsa_circ_210596,RMVar_hsa_circ_210593,RMVar_hsa_circ_210594,RMVar_hsa_circ_210592 13096 RMVar_ID_13096 Human_SNP_ID_683169720 A-to-I Human chr20 + 48959772 48959772 48959772 GCTGGGACTACAGGTGTGCCCTGCTGATTTTTATACTTTTTGTAGAGATGGGGTTTTGCTGTGTT GCTGGGACTACAGGTGTGCCCTGCTGATTTTTCTACTTTTTGTAGAGATGGGGTTTTGCTGTGTT A C ARFGEF2 Ensembl:ENSG00000124198 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1286915849 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39821,RMVar_hsa_circ_57380,RMVar_hsa_circ_12076,RMVar_hsa_circ_90847,RMVar_hsa_circ_8994,RMVar_hsa_circ_70925,RMVar_hsa_circ_5981,RMVar_hsa_circ_359,RMVar_hsa_circ_6503,RMVar_hsa_circ_66207,RMVar_hsa_circ_15654,RMVar_hsa_circ_113756,RMVar_hsa_circ_295586,RMVar_hsa_circ_322148,RMVar_hsa_circ_349851,RMVar_hsa_circ_125828,RMVar_hsa_circ_91898,RMVar_hsa_circ_104358,RMVar_hsa_circ_90229,RMVar_hsa_circ_210579,RMVar_hsa_circ_210581,RMVar_hsa_circ_53966,RMVar_hsa_circ_210582,RMVar_hsa_circ_210580,RMVar_hsa_circ_210577,RMVar_hsa_circ_210578,RMVar_hsa_circ_293164,RMVar_hsa_circ_343126,RMVar_hsa_circ_306847,RMVar_hsa_circ_98203,RMVar_hsa_circ_279429,RMVar_hsa_circ_210589,RMVar_hsa_circ_210590,RMVar_hsa_circ_210588,RMVar_hsa_circ_335277,RMVar_hsa_circ_293716,RMVar_hsa_circ_119777,RMVar_hsa_circ_272368,RMVar_hsa_circ_100541,RMVar_hsa_circ_96615,RMVar_hsa_circ_97813,RMVar_hsa_circ_93684,RMVar_hsa_circ_210591,RMVar_hsa_circ_41333,RMVar_hsa_circ_81582,RMVar_hsa_circ_87170,RMVar_hsa_circ_76773,RMVar_hsa_circ_210595,RMVar_hsa_circ_210599,RMVar_hsa_circ_210601,RMVar_hsa_circ_210602,RMVar_hsa_circ_210603,RMVar_hsa_circ_210600,RMVar_hsa_circ_210597,RMVar_hsa_circ_210598,RMVar_hsa_circ_210596,RMVar_hsa_circ_210593,RMVar_hsa_circ_210594,RMVar_hsa_circ_210592 13097 RMVar_ID_13097 Human_SNP_ID_683176409 A-to-I Human chr20 + 48986769 48986769 48986769 TTGCCCAGGTTGAAGTACAGTGGGGTGATCACAGATCACTGCAGCCTGGATCTCCTGGGCTCAAT TTGCCCAGGTTGAAGTACAGTGGGGTGATCACCGATCACTGCAGCCTGGATCTCCTGGGCTCAAT A C ARFGEF2 Ensembl:ENSG00000124198 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1477621963 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571703 RMVar_hsa_circ_57380,RMVar_hsa_circ_12076,RMVar_hsa_circ_90847,RMVar_hsa_circ_359,RMVar_hsa_circ_6503,RMVar_hsa_circ_15654,RMVar_hsa_circ_113756,RMVar_hsa_circ_125828,RMVar_hsa_circ_91898,RMVar_hsa_circ_104358,RMVar_hsa_circ_90229,RMVar_hsa_circ_210579,RMVar_hsa_circ_210581,RMVar_hsa_circ_53966,RMVar_hsa_circ_210580,RMVar_hsa_circ_210577,RMVar_hsa_circ_210578,RMVar_hsa_circ_98203,RMVar_hsa_circ_119777,RMVar_hsa_circ_100541,RMVar_hsa_circ_96615,RMVar_hsa_circ_97813,RMVar_hsa_circ_210591,RMVar_hsa_circ_81582,RMVar_hsa_circ_87170,RMVar_hsa_circ_76773,RMVar_hsa_circ_210595,RMVar_hsa_circ_210599,RMVar_hsa_circ_210597,RMVar_hsa_circ_210598,RMVar_hsa_circ_210596,RMVar_hsa_circ_210593,RMVar_hsa_circ_210594,RMVar_hsa_circ_210592,RMVar_hsa_circ_121409,RMVar_hsa_circ_121744,RMVar_hsa_circ_106064,RMVar_hsa_circ_67212,RMVar_hsa_circ_78496,RMVar_hsa_circ_91009,RMVar_hsa_circ_210607,RMVar_hsa_circ_210608,RMVar_hsa_circ_210609,RMVar_hsa_circ_210606,RMVar_hsa_circ_98543,RMVar_hsa_circ_123690,RMVar_hsa_circ_96420,RMVar_hsa_circ_210611,RMVar_hsa_circ_80953,RMVar_hsa_circ_210613,RMVar_hsa_circ_210614,RMVar_hsa_circ_210612,RMVar_hsa_circ_117935,RMVar_hsa_circ_210610,RMVar_hsa_circ_92270,RMVar_hsa_circ_93774,RMVar_hsa_circ_210617,RMVar_hsa_circ_210618,RMVar_hsa_circ_108619,RMVar_hsa_circ_127362,RMVar_hsa_circ_103067,RMVar_hsa_circ_210622,RMVar_hsa_circ_84317,RMVar_hsa_circ_3064,RMVar_hsa_circ_210623,RMVar_hsa_circ_210620,RMVar_hsa_circ_210621,RMVar_hsa_circ_210619,RMVar_hsa_circ_120905,RMVar_hsa_circ_119824,RMVar_hsa_circ_210629,RMVar_hsa_circ_210630,RMVar_hsa_circ_7255,RMVar_hsa_circ_73081,RMVar_hsa_circ_369080,RMVar_hsa_circ_57384,RMVar_hsa_circ_269456,RMVar_hsa_circ_266014,RMVar_hsa_circ_21950 13098 RMVar_ID_13098 Human_SNP_ID_683184803 A-to-I Human chr20 + 49020469 49020469 49020469 ATACCTTTTTCATTTTCTCTTTTTTTAGAGACAGGGACATACTCTGTCTCCCAAGCTGGAGTACA ATACCTTTTTCATTTTCTCTTTTTTTAGAGACCGGGACATACTCTGTCTCCCAAGCTGGAGTACA A C ARFGEF2 Ensembl:ENSG00000124198 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1187287207 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119777,RMVar_hsa_circ_210591,RMVar_hsa_circ_121409,RMVar_hsa_circ_210609,RMVar_hsa_circ_92270,RMVar_hsa_circ_210618,RMVar_hsa_circ_73081,RMVar_hsa_circ_57384,RMVar_hsa_circ_266014,RMVar_hsa_circ_109862,RMVar_hsa_circ_210636,RMVar_hsa_circ_99880,RMVar_hsa_circ_80833,RMVar_hsa_circ_118395,RMVar_hsa_circ_210637,RMVar_hsa_circ_210639,RMVar_hsa_circ_116872,RMVar_hsa_circ_210642,RMVar_hsa_circ_122855,RMVar_hsa_circ_210643,RMVar_hsa_circ_210644,RMVar_hsa_circ_85470,RMVar_hsa_circ_210646,RMVar_hsa_circ_104746,RMVar_hsa_circ_21659,RMVar_hsa_circ_89413,RMVar_hsa_circ_43580,RMVar_hsa_circ_210647,RMVar_hsa_circ_50716,RMVar_hsa_circ_210648 13099 RMVar_ID_13099 Human_SNP_ID_683187230 A-to-I Human chr20 + 49030075 49030075 49030075 GACTACAGGCGTGTGCCATCACACACCTGGCTAATTTTTGTGTTTTTAGTAGAGACAAAGTTTCA GACTACAGGCGTGTGCCATCACACACCTGGCTGATTTTTGTGTTTTTAGTAGAGACAAAGTTTCA A G ARFGEF2 Ensembl:ENSG00000124198 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs950249166 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121409,RMVar_hsa_circ_210609,RMVar_hsa_circ_266014,RMVar_hsa_circ_99880,RMVar_hsa_circ_210637,RMVar_hsa_circ_5717,RMVar_hsa_circ_361816,RMVar_hsa_circ_282997 13100 RMVar_ID_13100 Human_SNP_ID_683187552 A-to-I Human chr20 + 49031299 49031299 49031299 TCGCCCAGGCTGGAGTGCAGTGGTGCAATCTCAGTTTACTGCAACCTCCACCTCCTGAGTTCAAG TCGCCCAGGCTGGAGTGCAGTGGTGCAATCTCCGTTTACTGCAACCTCCACCTCCTGAGTTCAAG A C ARFGEF2 Ensembl:ENSG00000124198 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs923931167 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121409,RMVar_hsa_circ_210609,RMVar_hsa_circ_266014,RMVar_hsa_circ_99880,RMVar_hsa_circ_210637,RMVar_hsa_circ_5717,RMVar_hsa_circ_361816,RMVar_hsa_circ_282997 13101 RMVar_ID_13101 Human_SNP_ID_683187578 A-to-I Human chr20 + 49031432 49031432 49031432 TTCTATTTTTAGTAGAAATGGGGGTTTGCTACATTGGCCGGGCTGTCTCGAACTCCTGGCTTCAA TTCTATTTTTAGTAGAAATGGGGGTTTGCTACGTTGGCCGGGCTGTCTCGAACTCCTGGCTTCAA A G ARFGEF2 Ensembl:ENSG00000124198 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1287420069 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121409,RMVar_hsa_circ_210609,RMVar_hsa_circ_266014,RMVar_hsa_circ_99880,RMVar_hsa_circ_210637,RMVar_hsa_circ_5717,RMVar_hsa_circ_361816,RMVar_hsa_circ_282997 13102 RMVar_ID_13102 Human_SNP_ID_683189205 A-to-I Human chr20 - 49038561 49038561 49038561 CACCAAGTTGCTGATGAGTCTCTAGAAAGTACAAGGAGAATCCTGGGTTTAGCCATTGAGTCTCA CACCAAGTTGCTGATGAGTCTCTAGAAAGTACGAGGAGAATCCTGGGTTTAGCCATTGAGTCTCA T C SNAP23P1 Ensembl:ENSG00000230758 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1221502053 Functional Loss SNV dbSNP153 33..33 33 - - - 13103 RMVar_ID_13103 Human_SNP_ID_683192121 A-to-I Human chr20 + 49049296 49049296 49049296 CCTGGGCTGACCTGGGCTCAGTCTATCCTCCTACCTCAGCCTCCCGAGTAGCTAGGACTACAGGC CCTGGGCTGACCTGGGCTCAGTCTATCCTCCTGCCTCAGCCTCCCGAGTAGCTAGGACTACAGGC A G CSE1L Ensembl:ENSG00000124207 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1331223394 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108495,RMVar_hsa_circ_210655 13104 RMVar_ID_13104 Human_SNP_ID_683192122 A-to-I Human chr20 + 49049296 49049296 49049296 CCTGGGCTGACCTGGGCTCAGTCTATCCTCCTACCTCAGCCTCCCGAGTAGCTAGGACTACAGGC CCTGGGCTGACCTGGGCTCAGTCTATCCTCCTTCCTCAGCCTCCCGAGTAGCTAGGACTACAGGC A T CSE1L Ensembl:ENSG00000124207 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1331223394 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108495,RMVar_hsa_circ_210655 13105 RMVar_ID_13105 Human_SNP_ID_683192127 A-to-I Human chr20 + 49049317 49049317 49049317 TCTATCCTCCTACCTCAGCCTCCCGAGTAGCTAGGACTACAGGCGTGCACCACCACACTCAACTA TCTATCCTCCTACCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGTGCACCACCACACTCAACTA A G CSE1L Ensembl:ENSG00000124207 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1342220984 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108495,RMVar_hsa_circ_210655 13106 RMVar_ID_13106 Human_SNP_ID_683196293 A-to-I Human chr20 + 49064628 49064628 49064628 CCAGCCATTAGGGAGGCTGAGATGAGGGGATCACTTGTGCCTGGGAGGCAGAGGTTGCAATGAAC CCAGCCATTAGGGAGGCTGAGATGAGGGGATCCCTTGTGCCTGGGAGGCAGAGGTTGCAATGAAC A C CSE1L Ensembl:ENSG00000124207 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs953909545 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7008192,Human_RBP_ID_17658892 RMVar_hsa_circ_108260,RMVar_hsa_circ_44091,RMVar_hsa_circ_63246,RMVar_hsa_circ_368110,RMVar_hsa_circ_329602,RMVar_hsa_circ_300449,RMVar_hsa_circ_54423,RMVar_hsa_circ_55607,RMVar_hsa_circ_45416,RMVar_hsa_circ_314691,RMVar_hsa_circ_210657,RMVar_hsa_circ_210659,RMVar_hsa_circ_35885,RMVar_hsa_circ_210658,RMVar_hsa_circ_331130,RMVar_hsa_circ_298588,RMVar_hsa_circ_311150,RMVar_hsa_circ_298331,RMVar_hsa_circ_210660,RMVar_hsa_circ_28129,RMVar_hsa_circ_54008,RMVar_hsa_circ_210662,RMVar_hsa_circ_210663,RMVar_hsa_circ_210661 13107 RMVar_ID_13107 Human_SNP_ID_683196294 A-to-I Human chr20 + 49064628 49064628 49064628 CCAGCCATTAGGGAGGCTGAGATGAGGGGATCACTTGTGCCTGGGAGGCAGAGGTTGCAATGAAC CCAGCCATTAGGGAGGCTGAGATGAGGGGATCTCTTGTGCCTGGGAGGCAGAGGTTGCAATGAAC A T CSE1L Ensembl:ENSG00000124207 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs953909545 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7008192,Human_RBP_ID_17658892 RMVar_hsa_circ_108260,RMVar_hsa_circ_44091,RMVar_hsa_circ_63246,RMVar_hsa_circ_368110,RMVar_hsa_circ_329602,RMVar_hsa_circ_300449,RMVar_hsa_circ_54423,RMVar_hsa_circ_55607,RMVar_hsa_circ_45416,RMVar_hsa_circ_314691,RMVar_hsa_circ_210657,RMVar_hsa_circ_210659,RMVar_hsa_circ_35885,RMVar_hsa_circ_210658,RMVar_hsa_circ_331130,RMVar_hsa_circ_298588,RMVar_hsa_circ_311150,RMVar_hsa_circ_298331,RMVar_hsa_circ_210660,RMVar_hsa_circ_28129,RMVar_hsa_circ_54008,RMVar_hsa_circ_210662,RMVar_hsa_circ_210663,RMVar_hsa_circ_210661 13108 RMVar_ID_13108 Human_SNP_ID_683196736 A-to-I Human chr20 + 49065855 49065855 49065855 ACCTCAGGTGATCCACCTGCCTTGGCCTCTCAAAGTGCTGGGATTATAGGCGTGAGCCACTGCGC ACCTCAGGTGATCCACCTGCCTTGGCCTCTCAGAGTGCTGGGATTATAGGCGTGAGCCACTGCGC A G CSE1L Ensembl:ENSG00000124207 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1330787283 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108260,RMVar_hsa_circ_44091,RMVar_hsa_circ_63246,RMVar_hsa_circ_368110,RMVar_hsa_circ_329602,RMVar_hsa_circ_300449,RMVar_hsa_circ_54423,RMVar_hsa_circ_55607,RMVar_hsa_circ_45416,RMVar_hsa_circ_314691,RMVar_hsa_circ_210657,RMVar_hsa_circ_210659,RMVar_hsa_circ_35885,RMVar_hsa_circ_210658,RMVar_hsa_circ_331130,RMVar_hsa_circ_298588,RMVar_hsa_circ_311150,RMVar_hsa_circ_298331,RMVar_hsa_circ_210660,RMVar_hsa_circ_28129,RMVar_hsa_circ_54008,RMVar_hsa_circ_210662,RMVar_hsa_circ_210663,RMVar_hsa_circ_210661 13109 RMVar_ID_13109 Human_SNP_ID_683198984 A-to-I Human chr20 + 49074136 49074136 49074136 AAGCAGCTTAGGTGGGAGTTTTGCTTGAGCTCAGGAGGTGGAGGCTGCAGTGAGACATGATCATA AAGCAGCTTAGGTGGGAGTTTTGCTTGAGCTCGGGAGGTGGAGGCTGCAGTGAGACATGATCATA A G CSE1L Ensembl:ENSG00000124207 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1190144618 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7008277,Human_RBP_ID_8534951,Human_RBP_ID_23908565 RMVar_hsa_circ_690,RMVar_hsa_circ_108260,RMVar_hsa_circ_44091,RMVar_hsa_circ_54423,RMVar_hsa_circ_55607,RMVar_hsa_circ_45416,RMVar_hsa_circ_210659,RMVar_hsa_circ_35885,RMVar_hsa_circ_311150,RMVar_hsa_circ_275910,RMVar_hsa_circ_210660,RMVar_hsa_circ_28129,RMVar_hsa_circ_54008,RMVar_hsa_circ_210661,RMVar_hsa_circ_309720,RMVar_hsa_circ_329271,RMVar_hsa_circ_362310,RMVar_hsa_circ_315106,RMVar_hsa_circ_10091,RMVar_hsa_circ_273044,RMVar_hsa_circ_21075,RMVar_hsa_circ_210669,RMVar_hsa_circ_210671,RMVar_hsa_circ_210672,RMVar_hsa_circ_210670,RMVar_hsa_circ_210668,RMVar_hsa_circ_35759,RMVar_hsa_circ_342349,RMVar_hsa_circ_350171,RMVar_hsa_circ_346762,RMVar_hsa_circ_42721,RMVar_hsa_circ_22679,RMVar_hsa_circ_350425,RMVar_hsa_circ_375479,RMVar_hsa_circ_210673,RMVar_hsa_circ_308869,RMVar_hsa_circ_210679,RMVar_hsa_circ_210678,RMVar_hsa_circ_210681,RMVar_hsa_circ_210685,RMVar_hsa_circ_281786,RMVar_hsa_circ_331223,RMVar_hsa_circ_343724,RMVar_hsa_circ_376043,RMVar_hsa_circ_310285,RMVar_hsa_circ_275693,RMVar_hsa_circ_48725,RMVar_hsa_circ_210683,RMVar_hsa_circ_210684,RMVar_hsa_circ_210682,RMVar_hsa_circ_311883,RMVar_hsa_circ_29639,RMVar_hsa_circ_323371,RMVar_hsa_circ_338459,RMVar_hsa_circ_347805,RMVar_hsa_circ_322718,RMVar_hsa_circ_292593,RMVar_hsa_circ_24699,RMVar_hsa_circ_210686,RMVar_hsa_circ_210688,RMVar_hsa_circ_210689,RMVar_hsa_circ_210687,RMVar_hsa_circ_48667 13110 RMVar_ID_13110 Human_SNP_ID_683200660 A-to-I Human chr20 + 49079945 49079945 49079945 CTACTAAAAATACTAGCTGGGTGTGGTGGCACATGCCTATAATCCCATCTACTCGGGAGGCTGAG CTACTAAAAATACTAGCTGGGTGTGGTGGCACGTGCCTATAATCCCATCTACTCGGGAGGCTGAG A G CSE1L Ensembl:ENSG00000124207 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1050946008 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25617404 RMVar_hsa_circ_108260,RMVar_hsa_circ_44091,RMVar_hsa_circ_45416,RMVar_hsa_circ_210659,RMVar_hsa_circ_35885,RMVar_hsa_circ_210660,RMVar_hsa_circ_54008,RMVar_hsa_circ_329271,RMVar_hsa_circ_362310,RMVar_hsa_circ_10091,RMVar_hsa_circ_273044,RMVar_hsa_circ_21075,RMVar_hsa_circ_210671,RMVar_hsa_circ_210672,RMVar_hsa_circ_210670,RMVar_hsa_circ_342349,RMVar_hsa_circ_346762,RMVar_hsa_circ_42721,RMVar_hsa_circ_22679,RMVar_hsa_circ_375479,RMVar_hsa_circ_210673,RMVar_hsa_circ_210679,RMVar_hsa_circ_210685,RMVar_hsa_circ_281786,RMVar_hsa_circ_331223,RMVar_hsa_circ_310285,RMVar_hsa_circ_275693,RMVar_hsa_circ_210683,RMVar_hsa_circ_210684,RMVar_hsa_circ_210682,RMVar_hsa_circ_311883,RMVar_hsa_circ_323371,RMVar_hsa_circ_322718,RMVar_hsa_circ_292593,RMVar_hsa_circ_24699,RMVar_hsa_circ_210686,RMVar_hsa_circ_210688,RMVar_hsa_circ_210687,RMVar_hsa_circ_48667,RMVar_hsa_circ_286367,RMVar_hsa_circ_210691,RMVar_hsa_circ_210692,RMVar_hsa_circ_307699,RMVar_hsa_circ_282378,RMVar_hsa_circ_285371,RMVar_hsa_circ_210695,RMVar_hsa_circ_210697,RMVar_hsa_circ_210698,RMVar_hsa_circ_210696,RMVar_hsa_circ_210699,RMVar_hsa_circ_121929,RMVar_hsa_circ_210702,RMVar_hsa_circ_210704,RMVar_hsa_circ_301411,RMVar_hsa_circ_310610,RMVar_hsa_circ_336358,RMVar_hsa_circ_109443,RMVar_hsa_circ_210703,RMVar_hsa_circ_41671,RMVar_hsa_circ_210701 13111 RMVar_ID_13111 Human_SNP_ID_683210219 A-to-I Human chr20 - 49113721 49113721 49113721 TTAGGGCTGAAAAGAATGACCTACGTTTCTGTATACAGCTGTGTTGCTTTTGATGTTGTGTTACT TTAGGGCTGAAAAGAATGACCTACGTTTCTGTGTACAGCTGTGTTGCTTTTGATGTTGTGTTACT T C STAU1 Ensembl:ENSG00000124214 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1337779269 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_565749,Human_RBP_ID_1598504,Human_RBP_ID_1930998,Human_RBP_ID_2687209,Human_RBP_ID_3650549,Human_RBP_ID_7008695,Human_RBP_ID_8112720,Human_RBP_ID_8535046,Human_RBP_ID_14128670,Human_RBP_ID_17976809,Human_RBP_ID_18323085,Human_RBP_ID_23212322,Human_RBP_ID_23908680,Human_RBP_ID_26491275 13112 RMVar_ID_13112 Human_SNP_ID_683213762 A-to-I Human chr20 - 49126452 49126452 49126452 GTGATCCTCCTGTTTTAGCCTCCCACATAGCTAGGACTACATACAGGGGCACACTACCACACCTG GTGATCCTCCTGTTTTAGCCTCCCACATAGCTGGGACTACATACAGGGGCACACTACCACACCTG T C STAU1 Ensembl:ENSG00000124214 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017208250 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14128837 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_303409,RMVar_hsa_circ_321909,RMVar_hsa_circ_123744,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_81836,RMVar_hsa_circ_210733,RMVar_hsa_circ_65816,RMVar_hsa_circ_21386,RMVar_hsa_circ_365227,RMVar_hsa_circ_210734 13113 RMVar_ID_13113 Human_SNP_ID_683215997 A-to-I Human chr20 - 49134392 49134392 49134392 AGTTTCACTCTTGTCGCCCAGGCTGTAGTGCAATGGTGTGTTCTCGGCTCACTGCAACCTCCACC AGTTTCACTCTTGTCGCCCAGGCTGTAGTGCAGTGGTGTGTTCTCGGCTCACTGCAACCTCCACC T C STAU1 Ensembl:ENSG00000124214 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1195971034 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14128951 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_303409,RMVar_hsa_circ_321909,RMVar_hsa_circ_123744,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_81836,RMVar_hsa_circ_210733,RMVar_hsa_circ_65816,RMVar_hsa_circ_21386,RMVar_hsa_circ_365227,RMVar_hsa_circ_210734 13114 RMVar_ID_13114 Human_SNP_ID_683216517 A-to-I Human chr20 - 49136179 49136179 49136179 CTCCTGCCTCAGCCCTCCAAGTAGTTGGAACTACAGGCATGTACCACCACCACATCCACCTAAGT CTCCTGCCTCAGCCCTCCAAGTAGTTGGAACTGCAGGCATGTACCACCACCACATCCACCTAAGT T C STAU1 Ensembl:ENSG00000124214 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs898230755 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_346187,RMVar_hsa_circ_314425,RMVar_hsa_circ_85844,RMVar_hsa_circ_210723,RMVar_hsa_circ_210724,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_74881,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_210739,RMVar_hsa_circ_92031,RMVar_hsa_circ_210740,RMVar_hsa_circ_210738,RMVar_hsa_circ_210736 13115 RMVar_ID_13115 Human_SNP_ID_683224022 A-to-I Human chr20 - 49163488 49163488 49163488 CTGGGAGGCAGAGGCTGCAGCAAGCCAAGATCATGTCACCGCACTCCAGTCTGGGCAACAGAGCG CTGGGAGGCAGAGGCTGCAGCAAGCCAAGATCGTGTCACCGCACTCCAGTCTGGGCAACAGAGCG T C STAU1 Ensembl:ENSG00000124214 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs914442591 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10021426,Human_RBP_ID_18774784,Human_RBP_ID_25631082 RMVar_hsa_circ_346187,RMVar_hsa_circ_123744,RMVar_hsa_circ_210729,RMVar_hsa_circ_210735,RMVar_hsa_circ_106146,RMVar_hsa_circ_81836,RMVar_hsa_circ_210733,RMVar_hsa_circ_65816,RMVar_hsa_circ_210734,RMVar_hsa_circ_288841,RMVar_hsa_circ_303101,RMVar_hsa_circ_210737,RMVar_hsa_circ_210736,RMVar_hsa_circ_210742,RMVar_hsa_circ_210744,RMVar_hsa_circ_280211,RMVar_hsa_circ_319081,RMVar_hsa_circ_111014,RMVar_hsa_circ_210743,RMVar_hsa_circ_271020,RMVar_hsa_circ_359176 13116 RMVar_ID_13116 Human_SNP_ID_683226627 A-to-I Human chr20 - 49173412 49173412 49173412 AGTTTCGCTCTTGTTGCCCAGGTTGGAGTGCAATGGCGCCATGTTGGCTCACCTCGGCCTCCTGG AGTTTCGCTCTTGTTGCCCAGGTTGGAGTGCAGTGGCGCCATGTTGGCTCACCTCGGCCTCCTGG T C STAU1 Ensembl:ENSG00000124214 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs543538049 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571720 RMVar_hsa_circ_346187,RMVar_hsa_circ_123744,RMVar_hsa_circ_210729,RMVar_hsa_circ_210735,RMVar_hsa_circ_106146,RMVar_hsa_circ_81836,RMVar_hsa_circ_210733,RMVar_hsa_circ_65816,RMVar_hsa_circ_303101,RMVar_hsa_circ_210736,RMVar_hsa_circ_210746,RMVar_hsa_circ_210744,RMVar_hsa_circ_280211,RMVar_hsa_circ_111014,RMVar_hsa_circ_210743,RMVar_hsa_circ_271020,RMVar_hsa_circ_286474,RMVar_hsa_circ_210747 13117 RMVar_ID_13117 Human_SNP_ID_683227247 A-to-I Human chr20 - 49175542 49175542 49175542 CCGGGAGGCGGAGGTTGCAGGGAGCCGACATCACGCCACTGCACTCCATCCTGGGGGACAGGGTA CCGGGAGGCGGAGGTTGCAGGGAGCCGACATCGCGCCACTGCACTCCATCCTGGGGGACAGGGTA T C STAU1 Ensembl:ENSG00000124214 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1190762481 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571721,Human_RBP_ID_25631099 RMVar_hsa_circ_210735,RMVar_hsa_circ_106146,RMVar_hsa_circ_81836,RMVar_hsa_circ_210733,RMVar_hsa_circ_210744,RMVar_hsa_circ_111014,RMVar_hsa_circ_78839,RMVar_hsa_circ_210748 13118 RMVar_ID_13118 Human_SNP_ID_683227798 A-to-I Human chr20 - 49177183 49177183 49177183 ACCCTGGGCCAGGTGCGGTGGCTCACGCCTGTAATCGCAGCACTTTGGGAGGCCGAGGTGGGCGG ACCCTGGGCCAGGTGCGGTGGCTCACGCCTGTGATCGCAGCACTTTGGGAGGCCGAGGTGGGCGG T C STAU1 Ensembl:ENSG00000124214 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1326429040 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210735,RMVar_hsa_circ_106146,RMVar_hsa_circ_81836,RMVar_hsa_circ_210733,RMVar_hsa_circ_210744,RMVar_hsa_circ_111014,RMVar_hsa_circ_78839,RMVar_hsa_circ_210748 13119 RMVar_ID_13119 Human_SNP_ID_683228031 A-to-I Human chr20 - 49177924 49177924 49177924 GTTCTGTCTTGGCCTCCCAAAGTGTTGGGATTACAGGCGTGAGCCACCACACCTGGCCAAAACAT GTTCTGTCTTGGCCTCCCAAAGTGTTGGGATTGCAGGCGTGAGCCACCACACCTGGCCAAAACAT T C STAU1 Ensembl:ENSG00000124214 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs904913092 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210735,RMVar_hsa_circ_106146,RMVar_hsa_circ_81836,RMVar_hsa_circ_210733,RMVar_hsa_circ_210744,RMVar_hsa_circ_111014,RMVar_hsa_circ_78839,RMVar_hsa_circ_210748 13120 RMVar_ID_13120 Human_SNP_ID_683228060 A-to-I Human chr20 - 49178055 49178055 49178055 CTCCCATCTCAGCCTTCCAAGTAGCTGAGACTACAGGTGCATGCCATCATGCCTAGCTAGTTTTA CTCCCATCTCAGCCTTCCAAGTAGCTGAGACTGCAGGTGCATGCCATCATGCCTAGCTAGTTTTA T C STAU1 Ensembl:ENSG00000124214 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs919550660 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210735,RMVar_hsa_circ_106146,RMVar_hsa_circ_81836,RMVar_hsa_circ_210733,RMVar_hsa_circ_210744,RMVar_hsa_circ_111014,RMVar_hsa_circ_78839,RMVar_hsa_circ_210748 13121 RMVar_ID_13121 Human_SNP_ID_683228233 A-to-I Human chr20 - 49178699 49178696 49178699 TTACTCAGGCTGGAGTGCAGTGACCCAATCTCAGTTCACTGCAACCTCTGCCTCCCGGGTTCAAG TTACTCAGGCTGGAGTGCAGTGACCCAATCTC___TCACTGCAACCTCTGCCTCCCGGGTTCAAG AACT A STAU1 Ensembl:ENSG00000124214 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1413295320 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_210735,RMVar_hsa_circ_106146,RMVar_hsa_circ_81836,RMVar_hsa_circ_210733,RMVar_hsa_circ_210744,RMVar_hsa_circ_111014,RMVar_hsa_circ_78839,RMVar_hsa_circ_210748 13122 RMVar_ID_13122 Human_SNP_ID_683229080 A-to-I Human chr20 - 49181644 49181644 49181644 CTCCTGCCTTAGCCTCCCGAGTAGCTGAGACTACAATTGAGCACCACCACGCCCGGCTAATTTTT CTCCTGCCTTAGCCTCCCGAGTAGCTGAGACTGCAATTGAGCACCACCACGCCCGGCTAATTTTT T C STAU1 Ensembl:ENSG00000124214 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025212275 Functional Loss SNV dbSNP153 33..33 33 - - - 13123 RMVar_ID_13123 Human_SNP_ID_683243781 A-to-I Human chr20 + 49232087 49232087 49232087 TTATATTAAATAAATAGAGACGGGGTCTCGCTATGTTGTCAAGGCTGGTCTTGAACTCCTGGGCT TTATATTAAATAAATAGAGACGGGGTCTCGCTCTGTTGTCAAGGCTGGTCTTGAACTCCTGGGCT A C DDX27 Ensembl:ENSG00000124228 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs949943552 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116728,RMVar_hsa_circ_16260,RMVar_hsa_circ_118694,RMVar_hsa_circ_210751,RMVar_hsa_circ_210752,RMVar_hsa_circ_19186 13124 RMVar_ID_13124 Human_SNP_ID_683243782 A-to-I Human chr20 + 49232087 49232087 49232087 TTATATTAAATAAATAGAGACGGGGTCTCGCTATGTTGTCAAGGCTGGTCTTGAACTCCTGGGCT TTATATTAAATAAATAGAGACGGGGTCTCGCTGTGTTGTCAAGGCTGGTCTTGAACTCCTGGGCT A G DDX27 Ensembl:ENSG00000124228 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs949943552 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116728,RMVar_hsa_circ_16260,RMVar_hsa_circ_118694,RMVar_hsa_circ_210751,RMVar_hsa_circ_210752,RMVar_hsa_circ_19186 13125 RMVar_ID_13125 Human_SNP_ID_683248841 A-to-I Human chr20 - 49250899 49250899 49250899 CAAGACCATCCTGGCCAACATGGTGAAATCCCATCTCTACTAAAAATACAAAAATTAGCTGGGTG CAAGACCATCCTGGCCAACATGGTGAAATCCCGTCTCTACTAAAAATACAAAAATTAGCTGGGTG T C ZNFX1 Ensembl:ENSG00000124201 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1041337702 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98126,RMVar_hsa_circ_114846,RMVar_hsa_circ_123230,RMVar_hsa_circ_123625,RMVar_hsa_circ_121470,RMVar_hsa_circ_110700,RMVar_hsa_circ_112158,RMVar_hsa_circ_99395,RMVar_hsa_circ_210762,RMVar_hsa_circ_210766,RMVar_hsa_circ_95552,RMVar_hsa_circ_210768,RMVar_hsa_circ_78441,RMVar_hsa_circ_210767,RMVar_hsa_circ_210764,RMVar_hsa_circ_210765,RMVar_hsa_circ_210763,RMVar_hsa_circ_210760,RMVar_hsa_circ_210761,RMVar_hsa_circ_210759 13126 RMVar_ID_13126 Human_SNP_ID_683250920 A-to-I Human chr20 - 49258544 49258544 49258544 ACCTCAGCCTCCCAGAGTGCTGGGATACAGGCATAAGCCCCACGCACAGCCAAAACCTTTCTTTA ACCTCAGCCTCCCAGAGTGCTGGGATACAGGCCTAAGCCCCACGCACAGCCAAAACCTTTCTTTA T G ZNFX1 Ensembl:ENSG00000124201 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs552926958 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20897,RMVar_hsa_circ_123230,RMVar_hsa_circ_121470,RMVar_hsa_circ_110700,RMVar_hsa_circ_99395,RMVar_hsa_circ_210762,RMVar_hsa_circ_78441,RMVar_hsa_circ_210763,RMVar_hsa_circ_5791,RMVar_hsa_circ_210760,RMVar_hsa_circ_210761,RMVar_hsa_circ_210759,RMVar_hsa_circ_294923,RMVar_hsa_circ_57120,RMVar_hsa_circ_352241,RMVar_hsa_circ_46770,RMVar_hsa_circ_356543,RMVar_hsa_circ_45191,RMVar_hsa_circ_210770,RMVar_hsa_circ_269205,RMVar_hsa_circ_363713 13127 RMVar_ID_13127 Human_SNP_ID_683250922 A-to-I Human chr20 - 49258571 49258571 49258571 GAACTCCTGACGTCAGGTGATCCACCCACCTCAGCCTCCCAGAGTGCTGGGATACAGGCATAAGC GAACTCCTGACGTCAGGTGATCCACCCACCTCGGCCTCCCAGAGTGCTGGGATACAGGCATAAGC T C ZNFX1 Ensembl:ENSG00000124201 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1341250272 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20897,RMVar_hsa_circ_123230,RMVar_hsa_circ_121470,RMVar_hsa_circ_110700,RMVar_hsa_circ_99395,RMVar_hsa_circ_210762,RMVar_hsa_circ_78441,RMVar_hsa_circ_210763,RMVar_hsa_circ_5791,RMVar_hsa_circ_210760,RMVar_hsa_circ_210761,RMVar_hsa_circ_210759,RMVar_hsa_circ_294923,RMVar_hsa_circ_57120,RMVar_hsa_circ_352241,RMVar_hsa_circ_46770,RMVar_hsa_circ_356543,RMVar_hsa_circ_45191,RMVar_hsa_circ_210770,RMVar_hsa_circ_269205,RMVar_hsa_circ_363713 13128 RMVar_ID_13128 Human_SNP_ID_683251554 A-to-I Human chr20 - 49260959 49260959 49260959 CTTCTGCCTCAACCTCCTGAGTAGCTGGGACTACAGGCATGCACCACTATGCCTGGCTAATTTTT CTTCTGCCTCAACCTCCTGAGTAGCTGGGACTGCAGGCATGCACCACTATGCCTGGCTAATTTTT T C ZNFX1 Ensembl:ENSG00000124201 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1028192561 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123230,RMVar_hsa_circ_121470,RMVar_hsa_circ_110700,RMVar_hsa_circ_210762,RMVar_hsa_circ_78441,RMVar_hsa_circ_210760,RMVar_hsa_circ_210761,RMVar_hsa_circ_210759,RMVar_hsa_circ_294923,RMVar_hsa_circ_352241,RMVar_hsa_circ_46770,RMVar_hsa_circ_356543,RMVar_hsa_circ_45191,RMVar_hsa_circ_210770,RMVar_hsa_circ_269205,RMVar_hsa_circ_363713,RMVar_hsa_circ_33853,RMVar_hsa_circ_310287,RMVar_hsa_circ_334188,RMVar_hsa_circ_210771 13129 RMVar_ID_13129 Human_SNP_ID_683251898 A-to-I Human chr20 - 49262290 49262290 49262290 GCGATTCTCTTACCTTGGCCTCTTGAGTAGCTAGGATTACAGGCACCTGCCATCATGCCTGGCTA GCGATTCTCTTACCTTGGCCTCTTGAGTAGCTGGGATTACAGGCACCTGCCATCATGCCTGGCTA T C ZNFX1 Ensembl:ENSG00000124201 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1004654132 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123230,RMVar_hsa_circ_121470,RMVar_hsa_circ_110700,RMVar_hsa_circ_210762,RMVar_hsa_circ_78441,RMVar_hsa_circ_210760,RMVar_hsa_circ_210761,RMVar_hsa_circ_210759,RMVar_hsa_circ_294923,RMVar_hsa_circ_352241,RMVar_hsa_circ_46770,RMVar_hsa_circ_356543,RMVar_hsa_circ_45191,RMVar_hsa_circ_210770,RMVar_hsa_circ_269205,RMVar_hsa_circ_363713,RMVar_hsa_circ_33853,RMVar_hsa_circ_310287,RMVar_hsa_circ_334188,RMVar_hsa_circ_210771 13130 RMVar_ID_13130 Human_SNP_ID_683251899 A-to-I Human chr20 - 49262294 49262294 49262294 TCAAGCGATTCTCTTACCTTGGCCTCTTGAGTAGCTAGGATTACAGGCACCTGCCATCATGCCTG TCAAGCGATTCTCTTACCTTGGCCTCTTGAGTGGCTAGGATTACAGGCACCTGCCATCATGCCTG T C ZNFX1 Ensembl:ENSG00000124201 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1415856167 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123230,RMVar_hsa_circ_121470,RMVar_hsa_circ_110700,RMVar_hsa_circ_210762,RMVar_hsa_circ_78441,RMVar_hsa_circ_210760,RMVar_hsa_circ_210761,RMVar_hsa_circ_210759,RMVar_hsa_circ_294923,RMVar_hsa_circ_352241,RMVar_hsa_circ_46770,RMVar_hsa_circ_356543,RMVar_hsa_circ_45191,RMVar_hsa_circ_210770,RMVar_hsa_circ_269205,RMVar_hsa_circ_363713,RMVar_hsa_circ_33853,RMVar_hsa_circ_310287,RMVar_hsa_circ_334188,RMVar_hsa_circ_210771 13131 RMVar_ID_13131 Human_SNP_ID_683254658 A-to-I Human chr20 - 49273209 49273209 49273209 AGAATTGCTTGAACCCGGGAGGCGGAGGTTGCAGTGAGCCAAGATCATGCCACTGGACTCCAGCC AGAATTGCTTGAACCCGGGAGGCGGAGGTTGCGGTGAGCCAAGATCATGCCACTGGACTCCAGCC T C ZNFX1 Ensembl:ENSG00000124201 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs528444737 Functional Loss SNV dbSNP153 33..33 33 - - - 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 13132 RMVar_ID_13132 Human_SNP_ID_683254934 A-to-I Human chr20 - 49274507 49274507 49274507 GTGATCCACCCACCTTGGCCTCCCAAAGTGCTAGCATTACAGGCGTGAGCCACTGTGCCTGGCCT GTGATCCACCCACCTTGGCCTCCCAAAGTGCTGGCATTACAGGCGTGAGCCACTGTGCCTGGCCT T C ZNFX1 Ensembl:ENSG00000124201 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1200112295 Functional Loss SNV dbSNP153 33..33 33 - - - 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 13133 RMVar_ID_13133 Human_SNP_ID_683255025 A-to-I Human chr20 - 49274878 49274878 49274878 GACCTCGTGATCCGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCACGCC GACCTCGTGATCCGCCTGCCTCGGCCTCCCAAGGTGCTGGGATTACAGGCGTGAGCCACCACGCC T C ZNFX1 Ensembl:ENSG00000124201 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1490948203 Functional Loss SNV dbSNP153 33..33 33 - - - 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 13134 RMVar_ID_13134 Human_SNP_ID_683255253 A-to-I Human chr20 - 49275624 49275624 49275624 GGCTGGATGCAGTGGCTCAAGCCTATAATCCTAGCATTTTGGGAGCCTGAGGCGGGAGGATTGTT GGCTGGATGCAGTGGCTCAAGCCTATAATCCTTGCATTTTGGGAGCCTGAGGCGGGAGGATTGTT T A ZNFX1 Ensembl:ENSG00000124201 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1568988452 Functional Loss SNV dbSNP153 33..33 33 - - - 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 13135 RMVar_ID_13135 Human_SNP_ID_683255254 A-to-I Human chr20 - 49275632 49275632 49275632 ATGACTATGGCTGGATGCAGTGGCTCAAGCCTATAATCCTAGCATTTTGGGAGCCTGAGGCGGGA ATGACTATGGCTGGATGCAGTGGCTCAAGCCTTTAATCCTAGCATTTTGGGAGCCTGAGGCGGGA T A ZNFX1 Ensembl:ENSG00000124201 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1376563214 Functional Loss SNV dbSNP153 33..33 33 - - - 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 13136 RMVar_ID_13136 Human_SNP_ID_683345842 A-to-I Human chr20 - 49645190 49645190 49645190 TAGTGCTTGATCTTAGAGGTGGGGGTCTCACTATGTTGCCCAGGCTGGTCTCCAACTTCAGGGAG TAGTGCTTGATCTTAGAGGTGGGGGTCTCACTGTGTTGCCCAGGCTGGTCTCCAACTTCAGGGAG T C B4GALT5 Ensembl:ENSG00000158470 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1462822994 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101929,RMVar_hsa_circ_210787,RMVar_hsa_circ_336389,RMVar_hsa_circ_35987,RMVar_hsa_circ_351569,RMVar_hsa_circ_12878,RMVar_hsa_circ_342568,RMVar_hsa_circ_317642,RMVar_hsa_circ_210794,RMVar_hsa_circ_12341 13137 RMVar_ID_13137 Human_SNP_ID_683353218 A-to-I Human chr20 - 49675204 49675204 49675204 TTTGTTTGAGAGTAACAGCAATCTTAGGAATTAGTGATTTTTTTGGTCCTTGCAAATGTTACTGA TTTGTTTGAGAGTAACAGCAATCTTAGGAATTCGTGATTTTTTTGGTCCTTGCAAATGTTACTGA T G B4GALT5 Ensembl:ENSG00000158470 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1300780565 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14132195 RMVar_hsa_circ_101929,RMVar_hsa_circ_210787 13138 RMVar_ID_13138 Human_SNP_ID_683355032 A-to-I Human chr20 - 49682842 49682842 49682842 GTGATCCTCCTGCCTTAACCTCCTGAAGTGTTAGGATTGCAGATGTGAGCCACTGCGCCGGCCTA GTGATCCTCCTGCCTTAACCTCCTGAAGTGTTGGGATTGCAGATGTGAGCCACTGCGCCGGCCTA T C B4GALT5 Ensembl:ENSG00000158470 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1392688316 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14132293 RMVar_hsa_circ_101929,RMVar_hsa_circ_210787 13139 RMVar_ID_13139 Human_SNP_ID_683361331 A-to-I Human chr20 - 49707690 49707690 49707690 AGATCACCTGAGCCTGGGAGGTCGAGGCTGCAATGAGCCATGATTGAACCACTGCACTCTGTCTG AGATCACCTGAGCCTGGGAGGTCGAGGCTGCAGTGAGCCATGATTGAACCACTGCACTCTGTCTG T C B4GALT5 Ensembl:ENSG00000158470 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1356889091 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101929,RMVar_hsa_circ_210787 13140 RMVar_ID_13140 Human_SNP_ID_683361342 A-to-I Human chr20 - 49707722 49707719 49707722 TAATCCCAGCTACTCGGGAGGCTGAGGTCAGAAGATCACCTGAGCCTGGGAGGTCGAGGCTGCAA TAATCCCAGCTACTCGGGAGGCTGAGGTCAGA___TCACCTGAGCCTGGGAGGTCGAGGCTGCAA ATCT A B4GALT5 Ensembl:ENSG00000158470 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs983313957 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_101929,RMVar_hsa_circ_210787 13141 RMVar_ID_13141 Human_SNP_ID_683361858 A-to-I Human chr20 - 49709647 49709647 49709647 CTCCTGCTTCAGCCTCCAGAATAGCTGGGATTATAGGCGCTTGCCACCACTGGCTAATTTTTGTA CTCCTGCTTCAGCCTCCAGAATAGCTGGGATTGTAGGCGCTTGCCACCACTGGCTAATTTTTGTA T C B4GALT5 Ensembl:ENSG00000158470 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027219428 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101929,RMVar_hsa_circ_210787 13142 RMVar_ID_13142 Human_SNP_ID_683362190 A-to-I Human chr20 - 49710887 49710887 49710887 TTTTGTAGAGACAGGATCTCACTATGATGCACAGGCTCTGTTGAACTTAAATTTTTAGAATGTCT TTTTGTAGAGACAGGATCTCACTATGATGCACTGGCTCTGTTGAACTTAAATTTTTAGAATGTCT T A B4GALT5 Ensembl:ENSG00000158470 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs764192782 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14132880 RMVar_hsa_circ_101929,RMVar_hsa_circ_210787 13143 RMVar_ID_13143 Human_SNP_ID_683389567 A-to-I Human chr20 + 49816950 49816950 49816950 TGGCATTTCATTCTGTTGGCCAGGATGGTCTCAATCTCCTGACCTCGTGATCCACCTGCCTCGGC TGGCATTTCATTCTGTTGGCCAGGATGGTCTCGATCTCCTGACCTCGTGATCCACCTGCCTCGGC A G SLC9A8 Ensembl:ENSG00000197818 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1013930027 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210799,RMVar_hsa_circ_354052,RMVar_hsa_circ_7050 13144 RMVar_ID_13144 Human_SNP_ID_683392732 A-to-I Human chr20 - 49829598 49829598 49829598 TGAGCATGATATGGCTTCAGCTGTTTCACTTTAATCCAGGCATGATCTTATGTTCCAAAAAAATT TGAGCATGATATGGCTTCAGCTGTTTCACTTTGATCCAGGCATGATCTTATGTTCCAAAAAAATT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048984553 Functional Loss SNV dbSNP153 33..33 33 - - - 13145 RMVar_ID_13145 Human_SNP_ID_683392942 A-to-I Human chr20 - 49830419 49830419 49830419 CCAGCACCAGGTCCTTGGCCGCCTTGGGATCCAACACACGGGCGAAAGTGATGTCACAGGTTGAG CCAGCACCAGGTCCTTGGCCGCCTTGGGATCCCACACACGGGCGAAAGTGATGTCACAGGTTGAG T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs756307236 Functional Loss SNV dbSNP153 33..33 33 - - - 13146 RMVar_ID_13146 Human_SNP_ID_683403172 A-to-I Human chr20 + 49870820 49870820 49870820 ACCTCCCCAGGTTTAGGTGATCCTTCCACCTCAGCCTCCTGAGTAGCTGGGACTATAGGCACGTG ACCTCCCCAGGTTTAGGTGATCCTTCCACCTCCGCCTCCTGAGTAGCTGGGACTATAGGCACGTG A C SLC9A8 Ensembl:ENSG00000197818 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs756278149 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16947,RMVar_hsa_circ_333568,RMVar_hsa_circ_295585,RMVar_hsa_circ_210803,RMVar_hsa_circ_210804,RMVar_hsa_circ_40231,RMVar_hsa_circ_267681,RMVar_hsa_circ_321549,RMVar_hsa_circ_356370,RMVar_hsa_circ_45754,RMVar_hsa_circ_210808,RMVar_hsa_circ_66412,RMVar_hsa_circ_210809,RMVar_hsa_circ_47519,RMVar_hsa_circ_335512 13147 RMVar_ID_13147 Human_SNP_ID_683403173 A-to-I Human chr20 + 49870820 49870820 49870820 ACCTCCCCAGGTTTAGGTGATCCTTCCACCTCAGCCTCCTGAGTAGCTGGGACTATAGGCACGTG ACCTCCCCAGGTTTAGGTGATCCTTCCACCTCGGCCTCCTGAGTAGCTGGGACTATAGGCACGTG A G SLC9A8 Ensembl:ENSG00000197818 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs756278149 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16947,RMVar_hsa_circ_333568,RMVar_hsa_circ_295585,RMVar_hsa_circ_210803,RMVar_hsa_circ_210804,RMVar_hsa_circ_40231,RMVar_hsa_circ_267681,RMVar_hsa_circ_321549,RMVar_hsa_circ_356370,RMVar_hsa_circ_45754,RMVar_hsa_circ_210808,RMVar_hsa_circ_66412,RMVar_hsa_circ_210809,RMVar_hsa_circ_47519,RMVar_hsa_circ_335512 13148 RMVar_ID_13148 Human_SNP_ID_683403448 A-to-I Human chr20 + 49872115 49872115 49872115 CACTCCAGCCTGGGTGACAAGAGTGAAACTCCATCTCAAAGGAAAACAACAACAAAAACACTCTT CACTCCAGCCTGGGTGACAAGAGTGAAACTCCGTCTCAAAGGAAAACAACAACAAAAACACTCTT A G SLC9A8 Ensembl:ENSG00000197818 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs984680443 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16947,RMVar_hsa_circ_333568,RMVar_hsa_circ_295585,RMVar_hsa_circ_210803,RMVar_hsa_circ_210804,RMVar_hsa_circ_40231,RMVar_hsa_circ_267681,RMVar_hsa_circ_321549,RMVar_hsa_circ_356370,RMVar_hsa_circ_45754,RMVar_hsa_circ_210808,RMVar_hsa_circ_66412,RMVar_hsa_circ_210809,RMVar_hsa_circ_47519,RMVar_hsa_circ_335512 13149 RMVar_ID_13149 Human_SNP_ID_683413900 A-to-I Human chr20 - 49909548 49909548 49909548 GGACAGTTTCTTTTTCTTAAAAATTTTTTTGTATTTTTGTAGAGACGTGGTTTCACCGTGTTTCC GGACAGTTTCTTTTTCTTAAAAATTTTTTTGTTTTTTTGTAGAGACGTGGTTTCACCGTGTTTCC T A SPATA2 Ensembl:ENSG00000158480 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946244169 Functional Loss SNV dbSNP153 33..33 33 - - - 13150 RMVar_ID_13150 Human_SNP_ID_683422374 A-to-I Human chr20 + 49940693 49940693 49940693 CCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCGCCTGGCTGAGCTGAACCCTT CCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCCTGGCTGAGCTGAACCCTT A G RNF114 Ensembl:ENSG00000124226 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1260464640 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14133489 13151 RMVar_ID_13151 Human_SNP_ID_683422425 A-to-I Human chr20 + 49940845 49940845 49940845 TGTGCAGCCACCTCTGCCTCCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGG TGTGCAGCCACCTCTGCCTCCCAGGTTCAAGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGG A C RNF114 Ensembl:ENSG00000124226 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1304387310 Functional Loss SNV dbSNP153 33..33 33 - - - 13152 RMVar_ID_13152 Human_SNP_ID_683422442 A-to-I Human chr20 + 49940907 49940907 49940907 GGGATTACAGGCATCTGCCACCATGCCTGGCTAATTTTGGTATTTTTAGTAGAGACGGGTTTCAC GGGATTACAGGCATCTGCCACCATGCCTGGCTGATTTTGGTATTTTTAGTAGAGACGGGTTTCAC A G RNF114 Ensembl:ENSG00000124226 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1177050253 Functional Loss SNV dbSNP153 33..33 33 - - - 13153 RMVar_ID_13153 Human_SNP_ID_683422444 A-to-I Human chr20 + 49940922 49940922 49940922 TGCCACCATGCCTGGCTAATTTTGGTATTTTTAGTAGAGACGGGTTTCACCATGTTGGTAAGGCT TGCCACCATGCCTGGCTAATTTTGGTATTTTTGGTAGAGACGGGTTTCACCATGTTGGTAAGGCT A G RNF114 Ensembl:ENSG00000124226 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1032984788 Functional Loss SNV dbSNP153 33..33 33 - - - 13154 RMVar_ID_13154 Human_SNP_ID_683422889 A-to-I Human chr20 + 49942639 49942639 49942639 GAGTCCAGGAGTTCTAGACCAGCCTGGACAACATGGTGAAACCTCGGCTCTACTGAAAATACAAA GAGTCCAGGAGTTCTAGACCAGCCTGGACAACGTGGTGAAACCTCGGCTCTACTGAAAATACAAA A G RNF114 Ensembl:ENSG00000124226 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs901064171 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14133541 RMVar_hsa_circ_210815,RMVar_hsa_circ_61953,RMVar_hsa_circ_339337,RMVar_hsa_circ_210816,RMVar_hsa_circ_120413 13155 RMVar_ID_13155 Human_SNP_ID_683422923 A-to-I Human chr20 + 49942756 49942756 49942756 TGAGGTGAGAGGATGGCTTGAGCCCAGGAGGCAGAGGTTGCAGTGAGCTGAGTTCGTGCCACTGC TGAGGTGAGAGGATGGCTTGAGCCCAGGAGGCGGAGGTTGCAGTGAGCTGAGTTCGTGCCACTGC A G RNF114 Ensembl:ENSG00000124226 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1462000516 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210815,RMVar_hsa_circ_61953,RMVar_hsa_circ_339337,RMVar_hsa_circ_210816,RMVar_hsa_circ_120413 13156 RMVar_ID_13156 Human_SNP_ID_683423196 A-to-I Human chr20 + 49943728 49943728 49943728 TTGCCCAGGCTGGAGTACAGTGGCGTGATCTCAGCTCACTGCAGGCTCCGCCTGTTGGGTTCACG TTGCCCAGGCTGGAGTACAGTGGCGTGATCTCGGCTCACTGCAGGCTCCGCCTGTTGGGTTCACG A G RNF114 Ensembl:ENSG00000124226 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs912859371 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210815,RMVar_hsa_circ_61953,RMVar_hsa_circ_339337,RMVar_hsa_circ_210816,RMVar_hsa_circ_120413 13157 RMVar_ID_13157 Human_SNP_ID_683423382 A-to-I Human chr20 + 49943989 49943989 49943989 TGACCTCGTGACCCGCCCGCCTCAGCCTCCCAAAATGCTGGGATTATAGGCATGAGCCATTGCAC TGACCTCGTGACCCGCCCGCCTCAGCCTCCCAGAATGCTGGGATTATAGGCATGAGCCATTGCAC A G RNF114 Ensembl:ENSG00000124226 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1200708132 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210815,RMVar_hsa_circ_61953,RMVar_hsa_circ_339337,RMVar_hsa_circ_210816,RMVar_hsa_circ_120413 13158 RMVar_ID_13158 Human_SNP_ID_683423388 A-to-I Human chr20 + 49944008 49944008 49944008 CCTCAGCCTCCCAAAATGCTGGGATTATAGGCATGAGCCATTGCACCCGGTCTCTTCATCTTTAT CCTCAGCCTCCCAAAATGCTGGGATTATAGGCTTGAGCCATTGCACCCGGTCTCTTCATCTTTAT A T RNF114 Ensembl:ENSG00000124226 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1032275362 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7010091,Human_RBP_ID_14133598 RMVar_hsa_circ_210815,RMVar_hsa_circ_61953,RMVar_hsa_circ_339337,RMVar_hsa_circ_210816,RMVar_hsa_circ_120413 13159 RMVar_ID_13159 Human_SNP_ID_683423539 A-to-I Human chr20 + 49944631 49944631 49944631 GGCCGGGCGTGGTAGCTCACGCCTGTAAACCCAGCACTTTGGCAGGCTGAGGCAGGCAGATCACT GGCCGGGCGTGGTAGCTCACGCCTGTAAACCCCGCACTTTGGCAGGCTGAGGCAGGCAGATCACT A C RNF114 Ensembl:ENSG00000124226 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs950659896 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210815,RMVar_hsa_circ_61953,RMVar_hsa_circ_339337,RMVar_hsa_circ_210816,RMVar_hsa_circ_120413 13160 RMVar_ID_13160 Human_SNP_ID_683423547 A-to-I Human chr20 + 49944652 49944652 49944652 CCTGTAAACCCAGCACTTTGGCAGGCTGAGGCAGGCAGATCACTTGAGGTCAGGAGTTCGAGACC CCTGTAAACCCAGCACTTTGGCAGGCTGAGGCGGGCAGATCACTTGAGGTCAGGAGTTCGAGACC A G RNF114 Ensembl:ENSG00000124226 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,31158229,32596459 RNA-Seq:(High) rs1339530922 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25619091 RMVar_hsa_circ_210815,RMVar_hsa_circ_61953,RMVar_hsa_circ_339337,RMVar_hsa_circ_210816,RMVar_hsa_circ_120413 13161 RMVar_ID_13161 Human_SNP_ID_683423568 A-to-I Human chr20 + 49944760 49944759 49944760 AAAATTAGCTGGGCCTGATGGCACACACCTGTAATCCCAGCTACTCAGGAGGCTGAGGTGGGAGA AAAATTAGCTGGGCCTGATGGCACACACCTGT_ATCCCAGCTACTCAGGAGGCTGAGGTGGGAGA TA T RNF114 Ensembl:ENSG00000124226 Protein coding intron GSE47997;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,29129909,31158229,32596459,32596459 RNA-Seq:(High) rs1477574135 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_210815,RMVar_hsa_circ_61953,RMVar_hsa_circ_339337,RMVar_hsa_circ_210816,RMVar_hsa_circ_120413 13162 RMVar_ID_13162 Human_SNP_ID_683423569 A-to-I Human chr20 + 49944770 49944770 49944770 GGGCCTGATGGCACACACCTGTAATCCCAGCTACTCAGGAGGCTGAGGTGGGAGAATCACTTGAA GGGCCTGATGGCACACACCTGTAATCCCAGCTGCTCAGGAGGCTGAGGTGGGAGAATCACTTGAA A G RNF114 Ensembl:ENSG00000124226 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170659374 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210815,RMVar_hsa_circ_61953,RMVar_hsa_circ_339337,RMVar_hsa_circ_210816,RMVar_hsa_circ_120413 13163 RMVar_ID_13163 Human_SNP_ID_683461327 A-to-I Human chr20 - 50086919 50086919 50086919 GCGCCCACAACCACACCCGGCTAATGTTTTGTATTTTTAGTAGAGACAGGGTTTCACCGTGTTAG GCGCCCACAACCACACCCGGCTAATGTTTTGTGTTTTTAGTAGAGACAGGGTTTCACCGTGTTAG T C TMEM189-UBE2V1,UBE2V1 Ensembl:ENSG00000124208,Ensembl:ENSG00000244687 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1199501641 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15944 13164 RMVar_ID_13164 Human_SNP_ID_683462403 A-to-I Human chr20 - 50091144 50091144 50091144 TACTCAAGAGGCTGAGGAGGGAGAATCGCTTGAACCCAGGAGGCAGAGGTTTCAGTGGGCCAAGA TACTCAAGAGGCTGAGGAGGGAGAATCGCTTGCACCCAGGAGGCAGAGGTTTCAGTGGGCCAAGA T G TMEM189-UBE2V1,UBE2V1 Ensembl:ENSG00000124208,Ensembl:ENSG00000244687 Protein coding,Protein coding intron,intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs966000973 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15944 13165 RMVar_ID_13165 Human_SNP_ID_683462521 A-to-I Human chr20 - 50091562 50091562 50091562 ATGGCGAAACCCGGTCGCTACTAAAAAAGTATAAAAATTAGCTGGGCGCGGTGGCAGATGCCTGA ATGGCGAAACCCGGTCGCTACTAAAAAAGTATGAAAATTAGCTGGGCGCGGTGGCAGATGCCTGA T C TMEM189-UBE2V1,UBE2V1 Ensembl:ENSG00000124208,Ensembl:ENSG00000244687 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1314457575 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15944 13166 RMVar_ID_13166 Human_SNP_ID_683462663 A-to-I Human chr20 - 50092078 50092078 50092078 ACCTCAGGTGATCCGCCCACCTTGGTCTCTCAAAGTGCTGGGATTACAGGCATGAGCCCACCACA ACCTCAGGTGATCCGCCCACCTTGGTCTCTCACAGTGCTGGGATTACAGGCATGAGCCCACCACA T G TMEM189-UBE2V1,UBE2V1 Ensembl:ENSG00000124208,Ensembl:ENSG00000244687 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1205060029 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15944 13167 RMVar_ID_13167 Human_SNP_ID_683463063 A-to-I Human chr20 - 50093824 50093824 50093824 CCACCACGCCCAGCTAATTTTGTATTTTTAGTAGAGACGGGGTTTCACCATCTTAGCCAGGCTGG CCACCACGCCCAGCTAATTTTGTATTTTTAGTGGAGACGGGGTTTCACCATCTTAGCCAGGCTGG T C TMEM189-UBE2V1,UBE2V1 Ensembl:ENSG00000124208,Ensembl:ENSG00000244687 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs555105060 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15944 13168 RMVar_ID_13168 Human_SNP_ID_683469483 A-to-I Human chr20 - 50118825 50118825 50118825 GGTCAGGAATTCAAGACCAGCCTGGCCAACATAGTGAAACCCCGTCTCTACCAAAAATACAAAAG GGTCAGGAATTCAAGACCAGCCTGGCCAACATGGTGAAACCCCGTCTCTACCAAAAATACAAAAG T C TMEM189-UBE2V1,TMEM189 Ensembl:ENSG00000124208,Ensembl:ENSG00000240849 Protein coding,Protein coding intron,3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1226194828 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113111,RMVar_hsa_circ_210823 13169 RMVar_ID_13169 Human_SNP_ID_683469495 A-to-I Human chr20 - 50118897 50118897 50118897 AGTTCACATGTAAAAATGTGGCTGGGTGTGGTAGCTCACGCCTGTAATCCCAGCACTTTGGGCGG AGTTCACATGTAAAAATGTGGCTGGGTGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGCGG T C TMEM189-UBE2V1,TMEM189 Ensembl:ENSG00000124208,Ensembl:ENSG00000240849 Protein coding,Protein coding intron,3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs1362984172 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113111,RMVar_hsa_circ_210823 13170 RMVar_ID_13170 Human_SNP_ID_683469579 A-to-I Human chr20 - 50119312 50119312 50119312 CTCTCAGCCTCCCATCCCAAGTAGTTGGGACTACAGGTGCATGCCACCATGCTGAGCTAATTTTT CTCTCAGCCTCCCATCCCAAGTAGTTGGGACTGCAGGTGCATGCCACCATGCTGAGCTAATTTTT T C TMEM189-UBE2V1,TMEM189 Ensembl:ENSG00000124208,Ensembl:ENSG00000240849 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1475703105 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113111,RMVar_hsa_circ_210823 13171 RMVar_ID_13171 Human_SNP_ID_683469592 A-to-I Human chr20 - 50119405 50119405 50119405 TTGAGACAAAGTCTTGCTCTATTACCTGGGCTAGAGTGCAGTGGTGCAATCCCAGCTCACTACAG TTGAGACAAAGTCTTGCTCTATTACCTGGGCTGGAGTGCAGTGGTGCAATCCCAGCTCACTACAG T C TMEM189-UBE2V1,TMEM189 Ensembl:ENSG00000124208,Ensembl:ENSG00000240849 Protein coding,Protein coding intron,3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1057141897 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17395914 RMVar_hsa_circ_113111,RMVar_hsa_circ_210823 13172 RMVar_ID_13172 Human_SNP_ID_683469926 A-to-I Human chr20 - 50120752 50120752 50120752 TCACTGCAGACTCAACCTCCCAGGCTCAAGCAATCCTCCCATTTCAGCCTCTTGAATAGCGGGAA TCACTGCAGACTCAACCTCCCAGGCTCAAGCAGTCCTCCCATTTCAGCCTCTTGAATAGCGGGAA T C TMEM189-UBE2V1,TMEM189 Ensembl:ENSG00000124208,Ensembl:ENSG00000240849 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355418625 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113111,RMVar_hsa_circ_210823 13173 RMVar_ID_13173 Human_SNP_ID_683470407 A-to-I Human chr20 - 50122880 50122880 50122880 TTGTCCAGGTTGGTCTTGAACTCCTGGCCTCAAGTGATCCGCCTTGGCCTTCCAAAGTGCTGGAA TTGTCCAGGTTGGTCTTGAACTCCTGGCCTCAGGTGATCCGCCTTGGCCTTCCAAAGTGCTGGAA T C TMEM189-UBE2V1,TMEM189 Ensembl:ENSG00000124208,Ensembl:ENSG00000240849 Protein coding,Protein coding intron,3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1045656088 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113111,RMVar_hsa_circ_210823 13174 RMVar_ID_13174 Human_SNP_ID_683470452 A-to-I Human chr20 - 50123028 50123028 50123028 CTAAAGTGCAGAGGTGAGGTGTAATAGCTCACAGCAACCTTGAACTCCTGGACACAAACGATCCT CTAAAGTGCAGAGGTGAGGTGTAATAGCTCACGGCAACCTTGAACTCCTGGACACAAACGATCCT T C TMEM189-UBE2V1,TMEM189 Ensembl:ENSG00000124208,Ensembl:ENSG00000240849 Protein coding,Protein coding intron,3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1490198610 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14135178 RMVar_hsa_circ_113111,RMVar_hsa_circ_210823 13175 RMVar_ID_13175 Human_SNP_ID_683470574 A-to-I Human chr20 - 50123533 50123533 50123533 GGCCACGCACAGTGGCTCACGCCAGTAATCCCAGCACTTTGGGAGGCTGAGGCGGACAGATCACC GGCCACGCACAGTGGCTCACGCCAGTAATCCCGGCACTTTGGGAGGCTGAGGCGGACAGATCACC T C TMEM189-UBE2V1,TMEM189 Ensembl:ENSG00000124208,Ensembl:ENSG00000240849 Protein coding,Protein coding intron,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1022746773 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113111,RMVar_hsa_circ_210823 13176 RMVar_ID_13176 Human_SNP_ID_683650024 A-to-I Human chr20 + 50827942 50827942 50827942 AGAGACAGGGTTTCTCCATTTTGGCTGTGGCTAGTCTTGAACTCCTCACCTCAGGTGATCTGCCC AGAGACAGGGTTTCTCCATTTTGGCTGTGGCTGGTCTTGAACTCCTCACCTCAGGTGATCTGCCC A G BCAS4 Ensembl:ENSG00000124243 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs566019611 Functional Loss SNV dbSNP153 33..33 33 - - - 13177 RMVar_ID_13177 Human_SNP_ID_683653986 A-to-I Human chr20 + 50843983 50843983 50843983 CTGGGCAACATGGCAAAACCCCATTTATACAAAAAATAGAAAAGTTAGCTGGGCATGGTGGCGCA CTGGGCAACATGGCAAAACCCCATTTATACAAGAAATAGAAAAGTTAGCTGGGCATGGTGGCGCA A G BCAS4 Ensembl:ENSG00000124243 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs372015066 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105028,RMVar_hsa_circ_210843 13178 RMVar_ID_13178 Human_SNP_ID_683662642 A-to-I Human chr20 + 50877889 50877889 50877889 TGAGACCAGCCTGGGCAACATAATGAGACCATATCTCTACCAAAAATACAAAAATTAGCCTGGCG TGAGACCAGCCTGGGCAACATAATGAGACCATCTCTCTACCAAAAATACAAAAATTAGCCTGGCG A C BCAS4 Ensembl:ENSG00000124243 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1055762062 Functional Loss SNV dbSNP153 33..33 33 - - - 13179 RMVar_ID_13179 Human_SNP_ID_683662644 A-to-I Human chr20 + 50877906 50877906 50877906 ACATAATGAGACCATATCTCTACCAAAAATACAAAAATTAGCCTGGCGTGCTGGTGCACATCTGT ACATAATGAGACCATATCTCTACCAAAAATACTAAAATTAGCCTGGCGTGCTGGTGCACATCTGT A T BCAS4 Ensembl:ENSG00000124243 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs894483921 Functional Loss SNV dbSNP153 33..33 33 - - - 13180 RMVar_ID_13180 Human_SNP_ID_683662716 A-to-I Human chr20 + 50878269 50878269 50878269 TCAGCTCACTGCAACCTCCGCCTCCCGAGTTCAAGCTATTTTCCTGCCTCAGCCTCCCAGGAAGC TCAGCTCACTGCAACCTCCGCCTCCCGAGTTCGAGCTATTTTCCTGCCTCAGCCTCCCAGGAAGC A G BCAS4 Ensembl:ENSG00000124243 Protein coding 3'UTR GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line - 24183664,31158229 RNA-Seq:(High) rs1271487078 Functional Loss SNV dbSNP153 33..33 33 - - - 13181 RMVar_ID_13181 Human_SNP_ID_683662719 A-to-I Human chr20 + 50878287 50878281 50878287 CGCCTCCCGAGTTCAAGCTATTTTCCTGCCTCAGCCTCCCAGGAAGCTGGGATTACGGGAGCACA CGCCTCCCGAGTTCAAGCTATTTTCCT______GCCTCCCAGGAAGCTGGGATTACGGGAGCACA TGCCTCA T BCAS4 Ensembl:ENSG00000124243 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1263203092 Functional Loss DEL dbSNP153 28..33 33 - - - 13182 RMVar_ID_13182 Human_SNP_ID_683662753 A-to-I Human chr20 + 50878417 50878414 50878417 GTCTCGAACTCCTGACCTCAGGTGATCCTCCTACTTTGGCCTCCCAAGGTGCTGGGATTACAGGT GTCTCGAACTCCTGACCTCAGGTGATCCTC___CTTTGGCCTCCCAAGGTGCTGGGATTACAGGT CCTA C BCAS4 Ensembl:ENSG00000124243 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs758969705 Functional Loss DEL dbSNP153 31..33 33 - - - 13183 RMVar_ID_13183 Human_SNP_ID_683662804 A-to-I Human chr20 + 50878620 50878620 50878620 TCAAGTGATCCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACCACAAATGTGCACCACCATGCCTG TCAAGTGATCCTCCTGCCTCAGCCTCCCAAGTGGCTGGGACCACAAATGTGCACCACCATGCCTG A G BCAS4 Ensembl:ENSG00000124243 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1156314206 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_566360 13184 RMVar_ID_13184 Human_SNP_ID_683663300 A-to-I Human chr20 + 50880520 50880520 50880520 TTCTCTTTTTTAAACAGAGACGGGGTTTTGCTATGTTGTCCAGGCTAGTCTCAACCTCCTGGGCT TTCTCTTTTTTAAACAGAGACGGGGTTTTGCTGTGTTGTCCAGGCTAGTCTCAACCTCCTGGGCT A G BCAS4 Ensembl:ENSG00000124243 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1286810271 Functional Loss SNV dbSNP153 33..33 33 - - - 13185 RMVar_ID_13185 Human_SNP_ID_683663413 A-to-I Human chr20 + 50881110 50881110 50881110 GAAAAATTAGCCAGGCATGGTGGTGCTTGCCTATAGACCCAGCTACTTGGTGGGAGGTGGGAAGA GAAAAATTAGCCAGGCATGGTGGTGCTTGCCTGTAGACCCAGCTACTTGGTGGGAGGTGGGAAGA A G BCAS4 Ensembl:ENSG00000124243 Protein coding 3'UTR GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line - 24183664,31158229 RNA-Seq:(High) rs1242144696 Functional Loss SNV dbSNP153 33..33 33 - - - 13186 RMVar_ID_13186 Human_SNP_ID_683666507 A-to-I Human chr20 - 50892051 50892051 50892051 CAGTTTTGAAAATTTGGAAGAAGAATCCAATGAAAGTGGTAGCCCTTTTGACCCTGTTTTTGAAG CAGTTTTGAAAATTTGGAAGAAGAATCCAATGTAAGTGGTAGCCCTTTTGACCCTGTTTTTGAAG T A ADNP Ensembl:ENSG00000101126 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs769505609 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1599003,Human_RBP_ID_1931399,Human_RBP_ID_4664765,Human_RBP_ID_8535748,Human_RBP_ID_8855814,Human_RBP_ID_9118048,Human_RBP_ID_14137266,Human_RBP_ID_17973819,Human_RBP_ID_18775162,Human_RBP_ID_23909977,Human_RBP_ID_26343125 RMVar_hsa_circ_79070,RMVar_hsa_circ_104981,RMVar_hsa_circ_94612,RMVar_hsa_circ_210844,RMVar_hsa_circ_210845,RMVar_hsa_circ_210846 13187 RMVar_ID_13187 Human_SNP_ID_683666508 A-to-I Human chr20 - 50892051 50892051 50892051 CAGTTTTGAAAATTTGGAAGAAGAATCCAATGAAAGTGGTAGCCCTTTTGACCCTGTTTTTGAAG CAGTTTTGAAAATTTGGAAGAAGAATCCAATGGAAGTGGTAGCCCTTTTGACCCTGTTTTTGAAG T C ADNP Ensembl:ENSG00000101126 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs769505609 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1599003,Human_RBP_ID_1931399,Human_RBP_ID_4664765,Human_RBP_ID_8535748,Human_RBP_ID_8855814,Human_RBP_ID_9118048,Human_RBP_ID_14137266,Human_RBP_ID_17973819,Human_RBP_ID_18775162,Human_RBP_ID_23909977,Human_RBP_ID_26343125 RMVar_hsa_circ_79070,RMVar_hsa_circ_104981,RMVar_hsa_circ_94612,RMVar_hsa_circ_210844,RMVar_hsa_circ_210845,RMVar_hsa_circ_210846 13188 RMVar_ID_13188 Human_SNP_ID_683667799 A-to-I Human chr20 - 50896194 50896194 50896194 CTGAGACGGAGTCTCGCTGTGTTGCCCAGGCTAGAGTGCTGTGCTGTGATCTTGGCTCACTGCAA CTGAGACGGAGTCTCGCTGTGTTGCCCAGGCTGGAGTGCTGTGCTGTGATCTTGGCTCACTGCAA T C ADNP Ensembl:ENSG00000101126 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs112889768 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104981,RMVar_hsa_circ_94612,RMVar_hsa_circ_210845,RMVar_hsa_circ_210846 13189 RMVar_ID_13189 Human_SNP_ID_683667906 A-to-I Human chr20 - 50896520 50896520 50896520 GGTCTTGCTCTTGTCGCCCAGGCTGGAGTGCAATGGCACGATCTCAGCTCACTGCAACCTCAGTC GGTCTTGCTCTTGTCGCCCAGGCTGGAGTGCAGTGGCACGATCTCAGCTCACTGCAACCTCAGTC T C ADNP Ensembl:ENSG00000101126 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs138075146 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104981,RMVar_hsa_circ_94612,RMVar_hsa_circ_210845,RMVar_hsa_circ_210846 13190 RMVar_ID_13190 Human_SNP_ID_683668815 A-to-I Human chr20 - 50899614 50899614 50899614 CATCATTTCCTGTGATGGCAGTGTCGTCTTCTAGATACCTCCTGAAGGATCTGGCTGAGGCTGTT CATCATTTCCTGTGATGGCAGTGTCGTCTTCTGGATACCTCCTGAAGGATCTGGCTGAGGCTGTT T C ADNP Ensembl:ENSG00000101126 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1398529149 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104981,RMVar_hsa_circ_94612,RMVar_hsa_circ_210845,RMVar_hsa_circ_210846 13191 RMVar_ID_13191 Human_SNP_ID_683669011 A-to-I Human chr20 - 50900162 50900162 50900162 GAAGCATAGAAAAGGTACAGTAAAAATGCAATATAAAAGAAAAATTGGTACACCTATATTGGGCA GAAGCATAGAAAAGGTACAGTAAAAATGCAATGTAAAAGAAAAATTGGTACACCTATATTGGGCA T C ADNP Ensembl:ENSG00000101126 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1415284556 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104981,RMVar_hsa_circ_94612,RMVar_hsa_circ_210845,RMVar_hsa_circ_210846 13192 RMVar_ID_13192 Human_SNP_ID_683669039 A-to-I Human chr20 - 50900240 50900240 50900240 ACTATAAGAGAATACTATATACTGAATACTATAAGAGTGATTAACACAATGGTAAGTATTTGTGT ACTATAAGAGAATACTATATACTGAATACTATGAGAGTGATTAACACAATGGTAAGTATTTGTGT T C ADNP Ensembl:ENSG00000101126 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs3210876 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104981,RMVar_hsa_circ_94612,RMVar_hsa_circ_210845,RMVar_hsa_circ_210846 13193 RMVar_ID_13193 Human_SNP_ID_683670203 A-to-I Human chr20 - 50904493 50904493 50904493 TAGATATGTGCTCGGCTCAGTGGCTCACGCCTATAATCCCAGCACTTTGGGGTGCCAAGGCAGGA TAGATATGTGCTCGGCTCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGGTGCCAAGGCAGGA T C ADNP Ensembl:ENSG00000101126 Protein coding 5'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1029014734 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7011511,Human_RBP_ID_14137721,Human_RBP_ID_25619680 RMVar_hsa_circ_104981,RMVar_hsa_circ_94612,RMVar_hsa_circ_283150,RMVar_hsa_circ_210845,RMVar_hsa_circ_210846,RMVar_hsa_circ_294061,RMVar_hsa_circ_210849,RMVar_hsa_circ_210850,RMVar_hsa_circ_210848,RMVar_hsa_circ_210852,RMVar_hsa_circ_347441,RMVar_hsa_circ_289346 13194 RMVar_ID_13194 Human_SNP_ID_683670659 A-to-I Human chr20 - 50906207 50906206 50906207 AACTGTATGTGTTTTTTGTTTGTCTGTTTTTGAGATGGAATCTCGCTCTCGCCATGCTGGAGTGC AACTGTATGTGTTTTTTGTTTGTCTGTTTTTG_GATGGAATCTCGCTCTCGCCATGCTGGAGTGC CT C ADNP Ensembl:ENSG00000101126 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1266381781 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_3651166,Human_RBP_ID_14137805 RMVar_hsa_circ_104981,RMVar_hsa_circ_94612,RMVar_hsa_circ_210845,RMVar_hsa_circ_210846,RMVar_hsa_circ_294061,RMVar_hsa_circ_210849,RMVar_hsa_circ_210850,RMVar_hsa_circ_210852,RMVar_hsa_circ_289346,RMVar_hsa_circ_210853,RMVar_hsa_circ_298052 13195 RMVar_ID_13195 Human_SNP_ID_683671010 A-to-I Human chr20 - 50907391 50907391 50907391 GTGGTGGTACGCGCCTGTAGTCCCAGCTACTCAGGAGGTTGAGGAAGGAGAATTGCTTGAGCCTG GTGGTGGTACGCGCCTGTAGTCCCAGCTACTCCGGAGGTTGAGGAAGGAGAATTGCTTGAGCCTG T G ADNP Ensembl:ENSG00000101126 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031760255 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25619717 RMVar_hsa_circ_104981,RMVar_hsa_circ_94612,RMVar_hsa_circ_210845,RMVar_hsa_circ_210846,RMVar_hsa_circ_294061,RMVar_hsa_circ_210849,RMVar_hsa_circ_210850,RMVar_hsa_circ_210852,RMVar_hsa_circ_289346,RMVar_hsa_circ_210853,RMVar_hsa_circ_298052 13196 RMVar_ID_13196 Human_SNP_ID_683672049 A-to-I Human chr20 - 50910431 50910430 50910432 AGGTCCACACCCATGCTTTCTTATAGAAACATAGGTCTTGCTGTGTTGCTCAGTCTGGTCTTGAA AGGTCCACACCCATGCTTTCTTATAGAAACA__GGTCTTGCTGTGTTGCTCAGTCTGGTCTTGAA CTA C ADNP Ensembl:ENSG00000101126 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334937977 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_14137991,Human_RBP_ID_17571739 RMVar_hsa_circ_104981,RMVar_hsa_circ_94612,RMVar_hsa_circ_210845,RMVar_hsa_circ_210846,RMVar_hsa_circ_294061,RMVar_hsa_circ_210849,RMVar_hsa_circ_210850,RMVar_hsa_circ_210852,RMVar_hsa_circ_289346,RMVar_hsa_circ_210853,RMVar_hsa_circ_298052 13197 RMVar_ID_13197 Human_SNP_ID_683672126 A-to-I Human chr20 - 50910715 50910715 50910715 GGAGAATTGAGGCTGCAGTGAGCTGTGATCATACCACTGCACTCCAGCCTGGGTAACACAGAGTG GGAGAATTGAGGCTGCAGTGAGCTGTGATCATGCCACTGCACTCCAGCCTGGGTAACACAGAGTG T C ADNP Ensembl:ENSG00000101126 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs544105353 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23184703,Human_RBP_ID_25619766 RMVar_hsa_circ_104981,RMVar_hsa_circ_94612,RMVar_hsa_circ_210845,RMVar_hsa_circ_210846,RMVar_hsa_circ_294061,RMVar_hsa_circ_210849,RMVar_hsa_circ_210850,RMVar_hsa_circ_210852,RMVar_hsa_circ_289346,RMVar_hsa_circ_210853,RMVar_hsa_circ_298052 13198 RMVar_ID_13198 Human_SNP_ID_683672501 A-to-I Human chr20 + 50912093 50912093 50912093 AAGCATATCTAATATTGCACTGAGAGCTACACAAGGATCCTTACTTCTTCCTGGTTAACACCTAA AAGCATATCTAATATTGCACTGAGAGCTACACGAGGATCCTTACTTCTTCCTGGTTAACACCTAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs907844595 Functional Loss SNV dbSNP153 33..33 33 - - - 13199 RMVar_ID_13199 Human_SNP_ID_683672547 A-to-I Human chr20 - 50912284 50912284 50912284 AAATTAGCCCAGCCTGGTGGCGCGTGCCTGTAATCCCAGCTACTCGAGAGGCTGAGGTGGGAGAA AAATTAGCCCAGCCTGGTGGCGCGTGCCTGTATTCCCAGCTACTCGAGAGGCTGAGGTGGGAGAA T A ADNP Ensembl:ENSG00000101126 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1045191155 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104981,RMVar_hsa_circ_94612,RMVar_hsa_circ_210845,RMVar_hsa_circ_210846,RMVar_hsa_circ_294061,RMVar_hsa_circ_210849,RMVar_hsa_circ_210850,RMVar_hsa_circ_210852,RMVar_hsa_circ_289346,RMVar_hsa_circ_210853,RMVar_hsa_circ_298052 13200 RMVar_ID_13200 Human_SNP_ID_683672589 A-to-I Human chr20 - 50912423 50912423 50912423 GTTTGAAGCTAGGCGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGACAGGCAG GTTTGAAGCTAGGCGCAGTGGCTCACACCTGTGATCCCAGCACTTTGGGAGGCCAAGACAGGCAG T C ADNP Ensembl:ENSG00000101126 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs536752403 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104981,RMVar_hsa_circ_94612,RMVar_hsa_circ_210845,RMVar_hsa_circ_210846,RMVar_hsa_circ_294061,RMVar_hsa_circ_210849,RMVar_hsa_circ_210850,RMVar_hsa_circ_210852,RMVar_hsa_circ_289346,RMVar_hsa_circ_210853,RMVar_hsa_circ_298052 13201 RMVar_ID_13201 Human_SNP_ID_683674668 A-to-I Human chr20 - 50919419 50919419 50919419 CCAGGGTCTCCCTTTGTAACGCAGGCTGGAGTATAGTGGCACCATCATAGCTCACTGCAACTCAA CCAGGGTCTCCCTTTGTAACGCAGGCTGGAGTGTAGTGGCACCATCATAGCTCACTGCAACTCAA T C ADNP Ensembl:ENSG00000101126 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1362959038 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14138497 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 13202 RMVar_ID_13202 Human_SNP_ID_683674882 A-to-I Human chr20 - 50920092 50920092 50920092 TTGTATTTTTAGTAGAGATGGGGTTTCACCATATTCGCCAGGCTGGTCTCGAGCTCCTGACTTCG TTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTCGCCAGGCTGGTCTCGAGCTCCTGACTTCG T C ADNP Ensembl:ENSG00000101126 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1224035999 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14138543 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 13203 RMVar_ID_13203 Human_SNP_ID_683674887 A-to-I Human chr20 - 50920114 50920114 50920114 CACCACCACGCCCGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATATTCGCCAGGC CACCACCACGCCCGGCTAATTTTTGTATTTTTGGTAGAGATGGGGTTTCACCATATTCGCCAGGC T C ADNP Ensembl:ENSG00000101126 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs936730386 Functional Loss SNV dbSNP153 33..33 33 - - - 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 13204 RMVar_ID_13204 Human_SNP_ID_683675721 A-to-I Human chr20 - 50922720 50922720 50922720 AAAAAATTAGCTGGGTTTAGTGGTGGGGGCCTATAATCCCAGCTACTCAGGAGGCTGAGGCTGGA AAAAAATTAGCTGGGTTTAGTGGTGGGGGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCTGGA T C ADNP Ensembl:ENSG00000101126 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs558782243 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4652562 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 13205 RMVar_ID_13205 Human_SNP_ID_683677228 A-to-I Human chr20 - 50927691 50927691 50927691 TGGTTTTAACACTCAAAAAATAAGGTGAGGCCAGGTGAGGTGGCTTACGCCTGTAATCCCAAAAC TGGTTTTAACACTCAAAAAATAAGGTGAGGCCGGGTGAGGTGGCTTACGCCTGTAATCCCAAAAC T C ADNP Ensembl:ENSG00000101126 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs756518270 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_832036,Human_RBP_ID_7011849 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 13206 RMVar_ID_13206 Human_SNP_ID_683681998 A-to-I Human chr20 - 50943123 50943122 50943124 TCATGCAGGCTGGAGTGCAGTGGCGCAGTCTCAGTCACTGCAACCTCCACGTCCCGGGTTCAAGC TCATGCAGGCTGGAGTGCAGTGGCGCAGTCT__GTCACTGCAACCTCCACGTCCCGGGTTCAAGC CTG C DPM1 Ensembl:ENSG00000000419 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1049207638 Functional Loss DEL dbSNP153 32..33 33 - - - 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 13207 RMVar_ID_13207 Human_SNP_ID_683682667 A-to-I Human chr20 - 50945465 50945465 50945465 ACAATGGCATGCGCCTGTAGTCCCAGCTACTCAGGCGGCTCAGGTGGGAGGATGACATGAGCCCA ACAATGGCATGCGCCTGTAGTCCCAGCTACTCGGGCGGCTCAGGTGGGAGGATGACATGAGCCCA T C DPM1 Ensembl:ENSG00000000419 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs564032237 Functional Loss SNV dbSNP153 33..33 33 - - - 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 13208 RMVar_ID_13208 Human_SNP_ID_683682672 A-to-I Human chr20 - 50945494 50945494 50945494 ACAAAAAAAATAACAAAAATTAGCCAGACACAATGGCATGCGCCTGTAGTCCCAGCTACTCAGGC ACAAAAAAAATAACAAAAATTAGCCAGACACAGTGGCATGCGCCTGTAGTCCCAGCTACTCAGGC T C DPM1 Ensembl:ENSG00000000419 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1466044980 Functional Loss SNV dbSNP153 33..33 33 - - - 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 13209 RMVar_ID_13209 Human_SNP_ID_683683524 A-to-I Human chr20 - 50948953 50948953 50948953 TGGAGGCTGAGGCAGGAGAATCACTTTAACCCAGGAGGCAGAGGTTGCAGTGAGCGGAGATCACG TGGAGGCTGAGGCAGGAGAATCACTTTAACCCTGGAGGCAGAGGTTGCAGTGAGCGGAGATCACG T A DPM1 Ensembl:ENSG00000000419 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs562091210 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4301,RMVar_hsa_circ_310353,RMVar_hsa_circ_210864,RMVar_hsa_circ_210865,RMVar_hsa_circ_293392,RMVar_hsa_circ_7176 13210 RMVar_ID_13210 Human_SNP_ID_683683890 A-to-I Human chr20 - 50950634 50950634 50950634 TAACTCCTGACCTCAAATGATTCACCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG TAACTCCTGACCTCAAATGATTCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG T C DPM1 Ensembl:ENSG00000000419 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs970123142 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4301,RMVar_hsa_circ_310353,RMVar_hsa_circ_210864,RMVar_hsa_circ_210865,RMVar_hsa_circ_293392,RMVar_hsa_circ_7176 13211 RMVar_ID_13211 Human_SNP_ID_683683908 A-to-I Human chr20 - 50950722 50950722 50950722 GGGATTACAGGCACGTGCCACTACACCTGGCTAATTTTTGTATTTTTAGTAGAGATGAGGTCTCA GGGATTACAGGCACGTGCCACTACACCTGGCTGATTTTTGTATTTTTAGTAGAGATGAGGTCTCA T C DPM1 Ensembl:ENSG00000000419 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs950859530 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4301,RMVar_hsa_circ_310353,RMVar_hsa_circ_210864,RMVar_hsa_circ_210865,RMVar_hsa_circ_293392,RMVar_hsa_circ_7176 13212 RMVar_ID_13212 Human_SNP_ID_683698819 A-to-I Human chr20 - 51006805 51006805 51006805 GATTGGGGCTGGGTGCGGTGGCTCACGCCTGTAATCCCAGAACTTTGGGAGGCTGAGGCAGGCAG GATTGGGGCTGGGTGCGGTGGCTCACGCCTGTCATCCCAGAACTTTGGGAGGCTGAGGCAGGCAG T G KCNG1 Ensembl:ENSG00000026559 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs376067287 Functional Loss SNV dbSNP153 33..33 33 - - - 13213 RMVar_ID_13213 Human_SNP_ID_683698888 A-to-I Human chr20 - 51007087 51007087 51007087 CCTCAGCCTCCTGAATAGCTGGGACTAAAGGCATATGCCATCACACCCAGCTGGTAAAATCAACT CCTCAGCCTCCTGAATAGCTGGGACTAAAGGCGTATGCCATCACACCCAGCTGGTAAAATCAACT T C KCNG1 Ensembl:ENSG00000026559 Protein coding intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs933114995 Functional Loss SNV dbSNP153 33..33 33 - - - 13214 RMVar_ID_13214 Human_SNP_ID_683843116 A-to-I Human chr20 - 51590544 51590541 51590545 TTACATTAAAACAAACTTATTAATATAATAGAAAGCAGAATTTACTTGTGTTAAAAAAATATAGC TTACATTAAAACAAACTTATTAATATAATAG____CAGAATTTACTTGTGTTAAAAAAATATAGC GCTTT G - - Other Unknown GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1003838739 Functional Loss DEL dbSNP153 32..35 33 - - - 13215 RMVar_ID_13215 Human_SNP_ID_683853605 A-to-I Human chr20 - 51629547 51629547 51629547 GGTGTATGACTGGCATCTAGTGCGTAGGGGCCAGGGATGCTGCTCAACATTGTACAGTGCACAGG GGTGTATGACTGGCATCTAGTGCGTAGGGGCCTGGGATGCTGCTCAACATTGTACAGTGCACAGG T A ATP9A Ensembl:ENSG00000054793 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1024494655 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210880,RMVar_hsa_circ_86126,RMVar_hsa_circ_121249,RMVar_hsa_circ_122087,RMVar_hsa_circ_376871,RMVar_hsa_circ_116339,RMVar_hsa_circ_106769,RMVar_hsa_circ_78219,RMVar_hsa_circ_83892,RMVar_hsa_circ_80050,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_376319,RMVar_hsa_circ_122386,RMVar_hsa_circ_210897,RMVar_hsa_circ_210898,RMVar_hsa_circ_58520,RMVar_hsa_circ_104262,RMVar_hsa_circ_210901,RMVar_hsa_circ_210903,RMVar_hsa_circ_374510,RMVar_hsa_circ_77279,RMVar_hsa_circ_210906,RMVar_hsa_circ_210907,RMVar_hsa_circ_323600,RMVar_hsa_circ_376326,RMVar_hsa_circ_113227,RMVar_hsa_circ_210910,RMVar_hsa_circ_265851,RMVar_hsa_circ_49006,RMVar_hsa_circ_76249,RMVar_hsa_circ_210912,RMVar_hsa_circ_344720,RMVar_hsa_circ_210913,RMVar_hsa_circ_210914,RMVar_hsa_circ_93249,RMVar_hsa_circ_334289,RMVar_hsa_circ_210916,RMVar_hsa_circ_98647,RMVar_hsa_circ_126607,RMVar_hsa_circ_210915,RMVar_hsa_circ_344487,RMVar_hsa_circ_123087,RMVar_hsa_circ_210918,RMVar_hsa_circ_210919,RMVar_hsa_circ_210917 13216 RMVar_ID_13216 Human_SNP_ID_683873537 A-to-I Human chr20 - 51700277 51700277 51700277 GGCTCAAGTGGTCCACCTGTCTCAGCCTCCCAAAGTGCTGAGATTACAGGTTTGGGTCACTGTGT GGCTCAAGTGGTCCACCTGTCTCAGCCTCCCAGAGTGCTGAGATTACAGGTTTGGGTCACTGTGT T C ATP9A Ensembl:ENSG00000054793 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1470932314 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121249,RMVar_hsa_circ_78219,RMVar_hsa_circ_83892,RMVar_hsa_circ_210872,RMVar_hsa_circ_210874,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_126607,RMVar_hsa_circ_210919,RMVar_hsa_circ_346156,RMVar_hsa_circ_210920,RMVar_hsa_circ_369802,RMVar_hsa_circ_121118,RMVar_hsa_circ_210934,RMVar_hsa_circ_352063,RMVar_hsa_circ_210946,RMVar_hsa_circ_210947,RMVar_hsa_circ_4976,RMVar_hsa_circ_365646,RMVar_hsa_circ_310684,RMVar_hsa_circ_103357,RMVar_hsa_circ_210950,RMVar_hsa_circ_210955,RMVar_hsa_circ_52278 13217 RMVar_ID_13217 Human_SNP_ID_683880687 A-to-I Human chr20 - 51726845 51726845 51726845 TCTGGACGCAGTGGCTTAGGTCTGTAATCCCAACACTTTGGGAGGCTGAAGTGGGAGGATCGCTT TCTGGACGCAGTGGCTTAGGTCTGTAATCCCAGCACTTTGGGAGGCTGAAGTGGGAGGATCGCTT T C ATP9A Ensembl:ENSG00000054793 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs980751626 Functional Loss SNV dbSNP153 33..33 33 - - - 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 13218 RMVar_ID_13218 Human_SNP_ID_683892600 A-to-I Human chr20 - 51768324 51768324 51768324 TCCCGCTGCAGCCGGTGCGCCAGAAGAAGCGGATGGACAGCAGGCCCCGCGCCGGGTGAGTGGGC TCCCGCTGCAGCCGGTGCGCCAGAAGAAGCGGCTGGACAGCAGGCCCCGCGCCGGGTGAGTGGGC T G ATP9A Ensembl:ENSG00000054793 Protein coding start codon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1356412706 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244130,Human_RBP_ID_4659480 Human_Splice_Rec_2094769,Human_Splice_Rec_2094813 RMVar_hsa_circ_83892,RMVar_hsa_circ_210872,RMVar_hsa_circ_103357,RMVar_hsa_circ_210955 13219 RMVar_ID_13219 Human_SNP_ID_683905788 A-to-I Human chr20 - 51817258 51817258 51817258 AAAAAATTAGCTGGGTGTGGTGGTGCACGCCTATAATCCTGGCTACTGGCGAGGCTGAGGCAGAA AAAAAATTAGCTGGGTGTGGTGGTGCACGCCTGTAATCCTGGCTACTGGCGAGGCTGAGGCAGAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1475983033 Functional Loss SNV dbSNP153 33..33 33 - - - 13220 RMVar_ID_13220 Human_SNP_ID_683959169 A-to-I Human chr20 - 52020247 52020247 52020247 TCAAGTGATTCTCCTGCCCCAGCCTCCCAAGTAGCTGGCACTACAGGCACCTGCCGCCATGCCTG TCAAGTGATTCTCCTGCCCCAGCCTCCCAAGTTGCTGGCACTACAGGCACCTGCCGCCATGCCTG T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947756487 Functional Loss SNV dbSNP153 33..33 33 - - - 13221 RMVar_ID_13221 Human_SNP_ID_683969539 A-to-I Human chr20 - 52060559 52060559 52060559 CCAGCACTTTGGGAGGCCGAGGCAGGAGGATCACTTGAAGTCAGGAGTTCGAAACCAGCCTGGCC CCAGCACTTTGGGAGGCCGAGGCAGGAGGATCCCTTGAAGTCAGGAGTTCGAAACCAGCCTGGCC T G ZFP64 Ensembl:ENSG00000020256 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1188979431 Functional Loss SNV dbSNP153 33..33 33 - - - 13222 RMVar_ID_13222 Human_SNP_ID_683971525 A-to-I Human chr20 - 52069167 52069167 52069167 GGAGTGCAGTGGGTATTCTCCGGTGCAATCATAGCTCACTGCAGCCTCGAACTCCTGGGCTCAAG GGAGTGCAGTGGGTATTCTCCGGTGCAATCATGGCTCACTGCAGCCTCGAACTCCTGGGCTCAAG T C ZFP64 Ensembl:ENSG00000020256 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs563876282 Functional Loss SNV dbSNP153 33..33 33 - - - 13223 RMVar_ID_13223 Human_SNP_ID_683973756 A-to-I Human chr20 - 52077441 52077441 52077441 GATGTTAAGGCTGGGCATGGTGACTCACACCTATAACCCCAGTACTTTAGGAGGCCGAGGAGGGC GATGTTAAGGCTGGGCATGGTGACTCACACCTGTAACCCCAGTACTTTAGGAGGCCGAGGAGGGC T C ZFP64 Ensembl:ENSG00000020256 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1002463110 Functional Loss SNV dbSNP153 33..33 33 - - - 13224 RMVar_ID_13224 Human_SNP_ID_683974123 A-to-I Human chr20 - 52078856 52078856 52078856 GTTTTTGTATTTTCAGTAGAGACGGTTTCACCATGTTGCCCAGGCTGGTCTTGAACTCCTGACCT GTTTTTGTATTTTCAGTAGAGACGGTTTCACCGTGTTGCCCAGGCTGGTCTTGAACTCCTGACCT T C ZFP64 Ensembl:ENSG00000020256 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs568690548 Functional Loss SNV dbSNP153 33..33 33 - - - 13225 RMVar_ID_13225 Human_SNP_ID_683974137 A-to-I Human chr20 - 52078889 52078889 52078889 GGGATTATAGGCACATGTCACCATGCCTGGCTAGTTTTTGTATTTTCAGTAGAGACGGTTTCACC GGGATTATAGGCACATGTCACCATGCCTGGCTGGTTTTTGTATTTTCAGTAGAGACGGTTTCACC T C ZFP64 Ensembl:ENSG00000020256 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs768023919 Functional Loss SNV dbSNP153 33..33 33 - - - 13226 RMVar_ID_13226 Human_SNP_ID_684214694 A-to-I Human chr20 + 53038698 53038698 53038698 AACCGCTTTTTAACACATGTTGCTTAACACATATTTAATGAGGGTCTACCTGTACCAGGTGTGAA AACCGCTTTTTAACACATGTTGCTTAACACATGTTTAATGAGGGTCTACCTGTACCAGGTGTGAA A G TSHZ2 Ensembl:ENSG00000182463 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs779242281 Functional Loss SNV dbSNP153 33..33 33 - - - 13227 RMVar_ID_13227 Human_SNP_ID_684274210 A-to-I Human chr20 + 53272278 53272278 53272278 ATGGTCTGCCTGCCTCGGCCTCCCAAAGTGCTAGGATTACAGGCATGAACCACCGTGCCCGGCCG ATGGTCTGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAACCACCGTGCCCGGCCG A G TSHZ2 Ensembl:ENSG00000182463 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1439789403 Functional Loss SNV dbSNP153 33..33 33 - - - 13228 RMVar_ID_13228 Human_SNP_ID_684274542 A-to-I Human chr20 + 53273532 53273532 53273532 ACTGCTCTCGAACTCCTGACCTCAGGTGATCCACCTGCCTCGACTTTCCAAAGTGCTGGGATTAT ACTGCTCTCGAACTCCTGACCTCAGGTGATCCGCCTGCCTCGACTTTCCAAAGTGCTGGGATTAT A G TSHZ2 Ensembl:ENSG00000182463 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs557255708 Functional Loss SNV dbSNP153 33..33 33 - - - 13229 RMVar_ID_13229 Human_SNP_ID_684278933 A-to-I Human chr20 + 53291366 53291366 53291366 ATGGTGGCACACACCTGTATTCGCAGCTACTCAGGAAGCTGAGGCAGGAGAATCTATTGAACCTG ATGGTGGCACACACCTGTATTCGCAGCTACTCGGGAAGCTGAGGCAGGAGAATCTATTGAACCTG A G TSHZ2 Ensembl:ENSG00000182463 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1221393837 Functional Loss SNV dbSNP153 33..33 33 - - - 13230 RMVar_ID_13230 Human_SNP_ID_684279621 A-to-I Human chr20 + 53293901 53293901 53293901 AGCTGGGCGCAGTGGTGCATGTCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCT AGCTGGGCGCAGTGGTGCATGTCTGTAATCCCTGCTACTCGGGAGGCTGAGGCAGGAGAATTGCT A T TSHZ2 Ensembl:ENSG00000182463 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1343341194 Functional Loss SNV dbSNP153 33..33 33 - - - 13231 RMVar_ID_13231 Human_SNP_ID_684303452 A-to-I Human chr20 + 53391796 53391796 53391796 GAAACCCTGTCTCTACTAAAAATACAAAAATTAGACAGACGTGGTGGTGTGCACCTGTGATCCCA GAAACCCTGTCTCTACTAAAAATACAAAAATTCGACAGACGTGGTGGTGTGCACCTGTGATCCCA A C TSHZ2 Ensembl:ENSG00000182463 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1488313657 Functional Loss SNV dbSNP153 33..33 33 - - - 13232 RMVar_ID_13232 Human_SNP_ID_684303477 A-to-I Human chr20 + 53391875 53391875 53391875 TGAGGCACGAGAATTACTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCCAAGATGGTGCCACTGC TGAGGCACGAGAATTACTTGAACCTGGGAGGCCGAGGTTGCAGTGAGCCAAGATGGTGCCACTGC A C TSHZ2 Ensembl:ENSG00000182463 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1399453972 Functional Loss SNV dbSNP153 33..33 33 - - - 13233 RMVar_ID_13233 Human_SNP_ID_684312722 A-to-I Human chr20 + 53430850 53430850 53430850 GCGTGGTCTCGGCTCACTACCTCCTCCTCCCGAGTTCAACTGATTCTCCTGCCTCAGCCTCCCGA GCGTGGTCTCGGCTCACTACCTCCTCCTCCCGGGTTCAACTGATTCTCCTGCCTCAGCCTCCCGA A G TSHZ2 Ensembl:ENSG00000182463 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs960119572 Functional Loss SNV dbSNP153 33..33 33 - - - 13234 RMVar_ID_13234 Human_SNP_ID_684318832 A-to-I Human chr20 + 53454881 53454879 53454882 GACAGTATCAAGGAACTGAAACTTACCAGATCACCACATCTGAACAATGAGACAGAAGACCTCTC GACAGTATCAAGGAACTGAAACTTACCAGAT___CACATCTGAACAATGAGACAGAAGACCTCTC TCAC T TSHZ2 Ensembl:ENSG00000182463 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1304723667 Functional Loss DEL dbSNP153 32..34 33 - - - 13235 RMVar_ID_13235 Human_SNP_ID_684328426 A-to-I Human chr20 + 53488283 53488283 53488283 ATTTAACGTAAAAATTCCAATAGAACTGTATTAGATTTTCTCCATTAAATTAACGTTATGGATTT ATTTAACGTAAAAATTCCAATAGAACTGTATTCGATTTTCTCCATTAAATTAACGTTATGGATTT A C TSHZ2 Ensembl:ENSG00000182463 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1023627284 Functional Loss SNV dbSNP153 33..33 33 - - - 13236 RMVar_ID_13236 Human_SNP_ID_684328427 A-to-I Human chr20 + 53488283 53488283 53488283 ATTTAACGTAAAAATTCCAATAGAACTGTATTAGATTTTCTCCATTAAATTAACGTTATGGATTT ATTTAACGTAAAAATTCCAATAGAACTGTATTGGATTTTCTCCATTAAATTAACGTTATGGATTT A G TSHZ2 Ensembl:ENSG00000182463 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1023627284 Functional Loss SNV dbSNP153 33..33 33 - - - 13237 RMVar_ID_13237 Human_SNP_ID_684349941 A-to-I Human chr20 - 53565509 53565509 53565509 GGGAGGCAGAGGTTGGAGTGAGCCGAGATCGCACCACTGTACTCCGGCCTGAGCGACAGAGCGAG GGGAGGCAGAGGTTGGAGTGAGCCGAGATCGCCCCACTGTACTCCGGCCTGAGCGACAGAGCGAG T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs940940042 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2695583 13238 RMVar_ID_13238 Human_SNP_ID_684445882 A-to-I Human chr20 + 53916609 53916609 53916609 CAACTCTTAAGTTCAAGCGATTCTCGTACCCCAACCTCCCGAGTAGCTGGGATTACAGGCACCCG CAACTCTTAAGTTCAAGCGATTCTCGTACCCCGACCTCCCGAGTAGCTGGGATTACAGGCACCCG A G lnc-PFDN4-12 RNACentral:URS00008B67EC lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984240339 Functional Loss SNV dbSNP153 33..33 33 - - - 13239 RMVar_ID_13239 Human_SNP_ID_685081863 A-to-I Human chr20 - 56378405 56378405 56378405 ATTGCATTACAAATGTAGGAAATCACCTTACTAAAGGGCATGAGGGTAAAGTGTTGATCCAAGCA ATTGCATTACAAATGTAGGAAATCACCTTACTGAAGGGCATGAGGGTAAAGTGTTGATCCAAGCA T C AURKA Ensembl:ENSG00000087586 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1438051818 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108782,RMVar_hsa_circ_125358,RMVar_hsa_circ_211022,RMVar_hsa_circ_211023,RMVar_hsa_circ_4614 13240 RMVar_ID_13240 Human_SNP_ID_685081868 A-to-I Human chr20 - 56378425 56378425 56378425 ATTTTTACATTATATTTTACATTGCATTACAAATGTAGGAAATCACCTTACTAAAGGGCATGAGG ATTTTTACATTATATTTTACATTGCATTACAACTGTAGGAAATCACCTTACTAAAGGGCATGAGG T G AURKA Ensembl:ENSG00000087586 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1361794725 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14146186 RMVar_hsa_circ_108782,RMVar_hsa_circ_125358,RMVar_hsa_circ_211022,RMVar_hsa_circ_211023,RMVar_hsa_circ_4614 13241 RMVar_ID_13241 Human_SNP_ID_685084393 A-to-I Human chr20 - 56388620 56388620 56388620 TTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCTTGACCTCAGGTGATC TTTAGTAGAGACGGGGTTTCACCATGTTGGCCGGGCTGGTCTCGAACTCTTGACCTCAGGTGATC T C AURKA Ensembl:ENSG00000087586 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1304213429 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125358,RMVar_hsa_circ_211023,RMVar_hsa_circ_335191,RMVar_hsa_circ_360150,RMVar_hsa_circ_28372,RMVar_hsa_circ_7558 13242 RMVar_ID_13242 Human_SNP_ID_685084396 A-to-I Human chr20 - 56388629 56388629 56388629 TTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCTTGACCT TTTTGTATTTTTAGTAGAGACGGGGTTTCACCGTGTTGGCCAGGCTGGTCTCGAACTCTTGACCT T C AURKA Ensembl:ENSG00000087586 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs182506390 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125358,RMVar_hsa_circ_211023,RMVar_hsa_circ_335191,RMVar_hsa_circ_360150,RMVar_hsa_circ_28372,RMVar_hsa_circ_7558 13243 RMVar_ID_13243 Human_SNP_ID_685084397 A-to-I Human chr20 - 56388629 56388629 56388629 TTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCTTGACCT TTTTGTATTTTTAGTAGAGACGGGGTTTCACCCTGTTGGCCAGGCTGGTCTCGAACTCTTGACCT T G AURKA Ensembl:ENSG00000087586 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs182506390 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125358,RMVar_hsa_circ_211023,RMVar_hsa_circ_335191,RMVar_hsa_circ_360150,RMVar_hsa_circ_28372,RMVar_hsa_circ_7558 13244 RMVar_ID_13244 Human_SNP_ID_685084899 A-to-I Human chr20 - 56390486 56390486 56390486 CCCTACCAACATAGAGAAACCCTGTCTCTACTAAAAATACAAAATCAGCTGGGCGTGGTGGTGCA CCCTACCAACATAGAGAAACCCTGTCTCTACTGAAAATACAAAATCAGCTGGGCGTGGTGGTGCA T C AURKA Ensembl:ENSG00000087586 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs945646006 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125358,RMVar_hsa_circ_211023,RMVar_hsa_circ_335191,RMVar_hsa_circ_360150,RMVar_hsa_circ_28372,RMVar_hsa_circ_7558 13245 RMVar_ID_13245 Human_SNP_ID_685084902 A-to-I Human chr20 - 56390506 56390506 56390506 GGTCGGGAGTTCCAGACCAGCCCTACCAACATAGAGAAACCCTGTCTCTACTAAAAATACAAAAT GGTCGGGAGTTCCAGACCAGCCCTACCAACATGGAGAAACCCTGTCTCTACTAAAAATACAAAAT T C AURKA Ensembl:ENSG00000087586 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs760310647 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125358,RMVar_hsa_circ_211023,RMVar_hsa_circ_335191,RMVar_hsa_circ_360150,RMVar_hsa_circ_28372,RMVar_hsa_circ_7558 13246 RMVar_ID_13246 Human_SNP_ID_685085780 A-to-I Human chr20 + 56393338 56393338 56393338 AATTCACATAAGACGAATTAACAGATTACTGCAGGGTAAACAGGATGTGCATGTAAAGCATTGAG AATTCACATAAGACGAATTAACAGATTACTGCCGGGTAAACAGGATGTGCATGTAAAGCATTGAG A C CSTF1 Ensembl:ENSG00000101138 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1207218684 Functional Loss SNV dbSNP153 33..33 33 - - - 13247 RMVar_ID_13247 Human_SNP_ID_685085782 A-to-I Human chr20 + 56393347 56393347 56393347 AAGACGAATTAACAGATTACTGCAGGGTAAACAGGATGTGCATGTAAAGCATTGAGCTAGCATAC AAGACGAATTAACAGATTACTGCAGGGTAAACGGGATGTGCATGTAAAGCATTGAGCTAGCATAC A G CSTF1 Ensembl:ENSG00000101138 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1272983775 Functional Loss SNV dbSNP153 33..33 33 - - - 13248 RMVar_ID_13248 Human_SNP_ID_685085790 A-to-I Human chr20 + 56393378 56393378 56393378 CAGGATGTGCATGTAAAGCATTGAGCTAGCATACGGAAATTATTCGAGTCATATTAACCCAACGT CAGGATGTGCATGTAAAGCATTGAGCTAGCATGCGGAAATTATTCGAGTCATATTAACCCAACGT A G CSTF1 Ensembl:ENSG00000101138 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs531794012 Functional Loss SNV dbSNP153 33..33 33 - - - 13249 RMVar_ID_13249 Human_SNP_ID_685085800 A-to-I Human chr20 + 56393415 56393415 56393415 AATTATTCGAGTCATATTAACCCAACGTTAACAGTAGAATCTCTCATCAACTTTTCTTTGCCAGA AATTATTCGAGTCATATTAACCCAACGTTAACGGTAGAATCTCTCATCAACTTTTCTTTGCCAGA A G CSTF1 Ensembl:ENSG00000101138 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs546088109 Functional Loss SNV dbSNP153 33..33 33 - - - 13250 RMVar_ID_13250 Human_SNP_ID_685086227 A-to-I Human chr20 + 56395156 56395153 56395157 ATCTTGCATATTGCAGGTACCAGTCAATGTTTAATTAACAGAAGTAATGGAAGATTCTGGGATAA ATCTTGCATATTGCAGGTACCAGTCAATGT____TTAACAGAAGTAATGGAAGATTCTGGGATAA TTTAA T CSTF1 Ensembl:ENSG00000101138 Protein coding intron GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs1214473530 Functional Loss DEL dbSNP153 31..34 33 - - - 13251 RMVar_ID_13251 Human_SNP_ID_685088952 A-to-I Human chr20 + 56405307 56405307 56405307 CGGCTCACCGCAGCCTCCGCCACCTGGGTTCAAACGATTCTCCTGCCTCAGGCTCCCGAGTAACT CGGCTCACCGCAGCCTCCGCCACCTGGGTTCAGACGATTCTCCTGCCTCAGGCTCCCGAGTAACT A G CSTF1 Ensembl:ENSG00000101138 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs763401814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7014581,Human_RBP_ID_14146941 13252 RMVar_ID_13252 Human_SNP_ID_685335835 A-to-I Human chr20 + 57367485 57367485 57367485 ACTTTCTCGGCCAGGCATGGTAGCTCACGCCTATAATCCTAGCACTTTGGGAGGCAAAGGTGGGT ACTTTCTCGGCCAGGCATGGTAGCTCACGCCTGTAATCCTAGCACTTTGGGAGGCAAAGGTGGGT A G RAE1 Ensembl:ENSG00000101146 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs575858026 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16159,RMVar_hsa_circ_371362,RMVar_hsa_circ_81672,RMVar_hsa_circ_52954,RMVar_hsa_circ_106906,RMVar_hsa_circ_211048,RMVar_hsa_circ_211049,RMVar_hsa_circ_211050,RMVar_hsa_circ_74070 13253 RMVar_ID_13253 Human_SNP_ID_685335836 A-to-I Human chr20 + 57367485 57367485 57367485 ACTTTCTCGGCCAGGCATGGTAGCTCACGCCTATAATCCTAGCACTTTGGGAGGCAAAGGTGGGT ACTTTCTCGGCCAGGCATGGTAGCTCACGCCTTTAATCCTAGCACTTTGGGAGGCAAAGGTGGGT A T RAE1 Ensembl:ENSG00000101146 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs575858026 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16159,RMVar_hsa_circ_371362,RMVar_hsa_circ_81672,RMVar_hsa_circ_52954,RMVar_hsa_circ_106906,RMVar_hsa_circ_211048,RMVar_hsa_circ_211049,RMVar_hsa_circ_211050,RMVar_hsa_circ_74070 13254 RMVar_ID_13254 Human_SNP_ID_685336018 A-to-I Human chr20 + 57368028 57368028 57368028 TCTCCTGCTTCAGCCTCCCGTTAACTGGGACTACAGGTGTGTGCCACCAGGCCCAGCTAATTTTT TCTCCTGCTTCAGCCTCCCGTTAACTGGGACTGCAGGTGTGTGCCACCAGGCCCAGCTAATTTTT A G RAE1 Ensembl:ENSG00000101146 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs979198152 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16159,RMVar_hsa_circ_371362,RMVar_hsa_circ_81672,RMVar_hsa_circ_52954,RMVar_hsa_circ_106906,RMVar_hsa_circ_211048,RMVar_hsa_circ_211049,RMVar_hsa_circ_211050,RMVar_hsa_circ_74070 13255 RMVar_ID_13255 Human_SNP_ID_685434826 A-to-I Human chr20 + 57726997 57726997 57726997 ATCCGACTAATTTTTGTATTTTTAGTAGAGACAGGGCTTTGCCATGTTGGCCGGGCTGGTATCGA ATCCGACTAATTTTTGTATTTTTAGTAGAGACGGGGCTTTGCCATGTTGGCCGGGCTGGTATCGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1289964607 Functional Loss SNV dbSNP153 33..33 33 - - - 13256 RMVar_ID_13256 Human_SNP_ID_685585896 A-to-I Human chr20 + 58318102 58318102 58318102 ATTGCCCAGGCTGGTCTCGAACTCTTCACCTCAAGTGATCCTCCTGCCTTGGCCTCCCAAAGTGC ATTGCCCAGGCTGGTCTCGAACTCTTCACCTCGAGTGATCCTCCTGCCTTGGCCTCCCAAAGTGC A G RAB22A Ensembl:ENSG00000124209 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006012692 Functional Loss SNV dbSNP153 33..33 33 - - - 13257 RMVar_ID_13257 Human_SNP_ID_685762195 A-to-I Human chr20 - 58998446 58998446 58998446 TGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCACTGAGTAGCTGGGATTACAGGCATC TGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCGGCCTCCACTGAGTAGCTGGGATTACAGGCATC T C CTSZ Ensembl:ENSG00000101160 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1020064881 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57119,RMVar_hsa_circ_211100,RMVar_hsa_circ_302597,RMVar_hsa_circ_374806,RMVar_hsa_circ_211101 13258 RMVar_ID_13258 Human_SNP_ID_685762198 A-to-I Human chr20 - 58998459 58998459 58998459 TCACTGCAACCTCTGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCACTGAGTAGCTGG TCACTGCAACCTCTGCCTCCCGGGTTCAAGCGCTTCTCCTGCCTCAGCCTCCACTGAGTAGCTGG T G CTSZ Ensembl:ENSG00000101160 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1255889547 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57119,RMVar_hsa_circ_211100,RMVar_hsa_circ_302597,RMVar_hsa_circ_374806,RMVar_hsa_circ_211101 13259 RMVar_ID_13259 Human_SNP_ID_685762486 A-to-I Human chr20 - 58999315 58999315 58999315 TGATTGTGTGACTGGTGACCGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGC TGATTGTGTGACTGGTGACCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGC T C CTSZ Ensembl:ENSG00000101160 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1016613843 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57119,RMVar_hsa_circ_211100,RMVar_hsa_circ_302597,RMVar_hsa_circ_374806,RMVar_hsa_circ_211101 13260 RMVar_ID_13260 Human_SNP_ID_685762758 A-to-I Human chr20 - 59000175 59000175 59000175 CGGGGTTTCTCCATGTTGTTCAGGCTGGTCTTAAACTCCCAACCTCAAGTGATCCACCTGCCTTG CGGGGTTTCTCCATGTTGTTCAGGCTGGTCTTGAACTCCCAACCTCAAGTGATCCACCTGCCTTG T C CTSZ Ensembl:ENSG00000101160 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs747338588 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57119,RMVar_hsa_circ_211100,RMVar_hsa_circ_302597,RMVar_hsa_circ_374806,RMVar_hsa_circ_211101 13261 RMVar_ID_13261 Human_SNP_ID_685917578 A-to-I Human chr20 + 59612524 59612524 59612524 CTCCTGCCTCAGCCTCCCGAGTGGCTGGGACTACAGGTGCGCGCCACCATGCCCAACTAATTTTT CTCCTGCCTCAGCCTCCCGAGTGGCTGGGACTCCAGGTGCGCGCCACCATGCCCAACTAATTTTT A C PHACTR3 Ensembl:ENSG00000087495 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs940220592 Functional Loss SNV dbSNP153 33..33 33 - - - 13262 RMVar_ID_13262 Human_SNP_ID_685917579 A-to-I Human chr20 + 59612524 59612524 59612524 CTCCTGCCTCAGCCTCCCGAGTGGCTGGGACTACAGGTGCGCGCCACCATGCCCAACTAATTTTT CTCCTGCCTCAGCCTCCCGAGTGGCTGGGACTGCAGGTGCGCGCCACCATGCCCAACTAATTTTT A G PHACTR3 Ensembl:ENSG00000087495 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs940220592 Functional Loss SNV dbSNP153 33..33 33 - - - 13263 RMVar_ID_13263 Human_SNP_ID_15532359 A-to-I Human chr1 + 61101167 61101167 61101167 CCTGTAATCCCGGCACTTTGGGAGGCTGAGGCAGGCACATCACCTGAGGTCGGGAGTTCGAGATC CCTGTAATCCCGGCACTTTGGGAGGCTGAGGCGGGCACATCACCTGAGGTCGGGAGTTCGAGATC A G NFIA Ensembl:ENSG00000162599 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1166530609 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112289,RMVar_hsa_circ_133391,RMVar_hsa_circ_297271,RMVar_hsa_circ_133393,RMVar_hsa_circ_373526,RMVar_hsa_circ_341815,RMVar_hsa_circ_357209,RMVar_hsa_circ_374796,RMVar_hsa_circ_354102,RMVar_hsa_circ_7738,RMVar_hsa_circ_293382,RMVar_hsa_circ_133396,RMVar_hsa_circ_133397,RMVar_hsa_circ_133395 13264 RMVar_ID_13264 Human_SNP_ID_15535271 A-to-I Human chr1 + 61113528 61113528 61113528 AGGCAGGAGAATTGCTTGAACCGTTGAGGCGGAGGTTGTAATGAGCTGAGAGTGCACCATTGCAC AGGCAGGAGAATTGCTTGAACCGTTGAGGCGGGGGTTGTAATGAGCTGAGAGTGCACCATTGCAC A G NFIA Ensembl:ENSG00000162599 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1399048205 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11050200,Human_RBP_ID_17100777,Human_RBP_ID_23405235 RMVar_hsa_circ_112289,RMVar_hsa_circ_133391,RMVar_hsa_circ_297271,RMVar_hsa_circ_133393,RMVar_hsa_circ_373526,RMVar_hsa_circ_341815,RMVar_hsa_circ_357209,RMVar_hsa_circ_374796,RMVar_hsa_circ_354102,RMVar_hsa_circ_7738,RMVar_hsa_circ_293382,RMVar_hsa_circ_133396,RMVar_hsa_circ_133397,RMVar_hsa_circ_133402,RMVar_hsa_circ_133403,RMVar_hsa_circ_133401 13265 RMVar_ID_13265 Human_SNP_ID_15538814 A-to-I Human chr1 + 61128477 61128477 61128477 TACCGAAAAATACAAAAATTAGCCATGCTTGTAGTCCTAGCTATTAATACGTGGGAGGCTGAGGT TACCGAAAAATACAAAAATTAGCCATGCTTGTGGTCCTAGCTATTAATACGTGGGAGGCTGAGGT A G NFIA Ensembl:ENSG00000162599 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1351660945 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11051008 RMVar_hsa_circ_112289,RMVar_hsa_circ_133391,RMVar_hsa_circ_297271,RMVar_hsa_circ_133393,RMVar_hsa_circ_373526,RMVar_hsa_circ_341815,RMVar_hsa_circ_357209,RMVar_hsa_circ_374796,RMVar_hsa_circ_354102,RMVar_hsa_circ_7738,RMVar_hsa_circ_293382,RMVar_hsa_circ_133396,RMVar_hsa_circ_133397,RMVar_hsa_circ_133402,RMVar_hsa_circ_133403,RMVar_hsa_circ_133401 13266 RMVar_ID_13266 Human_SNP_ID_15538998 A-to-I Human chr1 + 61129002 61129002 61129002 TGGAGTGCAGTGACACGATCTCGGCTCACTGCAAGCTCCGCCTCCCAGATTCACGCCATTCTCCT TGGAGTGCAGTGACACGATCTCGGCTCACTGCTAGCTCCGCCTCCCAGATTCACGCCATTCTCCT A T NFIA Ensembl:ENSG00000162599 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1445587063 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112289,RMVar_hsa_circ_133391,RMVar_hsa_circ_297271,RMVar_hsa_circ_133393,RMVar_hsa_circ_373526,RMVar_hsa_circ_341815,RMVar_hsa_circ_357209,RMVar_hsa_circ_374796,RMVar_hsa_circ_354102,RMVar_hsa_circ_7738,RMVar_hsa_circ_293382,RMVar_hsa_circ_133396,RMVar_hsa_circ_133397,RMVar_hsa_circ_133402,RMVar_hsa_circ_133403,RMVar_hsa_circ_133401 13267 RMVar_ID_13267 Human_SNP_ID_15539007 A-to-I Human chr1 + 61129016 61129016 61129016 ACGATCTCGGCTCACTGCAAGCTCCGCCTCCCAGATTCACGCCATTCTCCTGCCTCAGCCTCCTG ACGATCTCGGCTCACTGCAAGCTCCGCCTCCCGGATTCACGCCATTCTCCTGCCTCAGCCTCCTG A G NFIA Ensembl:ENSG00000162599 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs902531340 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112289,RMVar_hsa_circ_133391,RMVar_hsa_circ_297271,RMVar_hsa_circ_133393,RMVar_hsa_circ_373526,RMVar_hsa_circ_341815,RMVar_hsa_circ_357209,RMVar_hsa_circ_374796,RMVar_hsa_circ_354102,RMVar_hsa_circ_7738,RMVar_hsa_circ_293382,RMVar_hsa_circ_133396,RMVar_hsa_circ_133397,RMVar_hsa_circ_133402,RMVar_hsa_circ_133403,RMVar_hsa_circ_133401 13268 RMVar_ID_13268 Human_SNP_ID_15539008 A-to-I Human chr1 + 61129018 61129018 61129018 GATCTCGGCTCACTGCAAGCTCCGCCTCCCAGATTCACGCCATTCTCCTGCCTCAGCCTCCTGAG GATCTCGGCTCACTGCAAGCTCCGCCTCCCAGGTTCACGCCATTCTCCTGCCTCAGCCTCCTGAG A G NFIA Ensembl:ENSG00000162599 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs999578383 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112289,RMVar_hsa_circ_133391,RMVar_hsa_circ_297271,RMVar_hsa_circ_133393,RMVar_hsa_circ_373526,RMVar_hsa_circ_341815,RMVar_hsa_circ_357209,RMVar_hsa_circ_374796,RMVar_hsa_circ_354102,RMVar_hsa_circ_7738,RMVar_hsa_circ_293382,RMVar_hsa_circ_133396,RMVar_hsa_circ_133397,RMVar_hsa_circ_133402,RMVar_hsa_circ_133403,RMVar_hsa_circ_133401 13269 RMVar_ID_13269 Human_SNP_ID_15544407 A-to-I Human chr1 + 61151230 61151230 61151230 TTGTTGTTGTTGTTTGTTTGTTTGTTTTTTTGAGACAGTCTCCACTCCGTTGCCCAGGCTGGAGT TTGTTGTTGTTGTTTGTTTGTTTGTTTTTTTGGGACAGTCTCCACTCCGTTGCCCAGGCTGGAGT A G NFIA Ensembl:ENSG00000162599 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs971604363 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2157963,Human_RBP_ID_3318390,Human_RBP_ID_5846738,Human_RBP_ID_11052311,Human_RBP_ID_18578661 RMVar_hsa_circ_112289,RMVar_hsa_circ_133391,RMVar_hsa_circ_297271,RMVar_hsa_circ_133393,RMVar_hsa_circ_373526,RMVar_hsa_circ_341815,RMVar_hsa_circ_357209,RMVar_hsa_circ_374796,RMVar_hsa_circ_354102,RMVar_hsa_circ_7738,RMVar_hsa_circ_293382,RMVar_hsa_circ_133396,RMVar_hsa_circ_133397,RMVar_hsa_circ_133402,RMVar_hsa_circ_133403,RMVar_hsa_circ_133404 13270 RMVar_ID_13270 Human_SNP_ID_15549949 A-to-I Human chr1 + 61175281 61175281 61175281 CTCTTGCCTCAGTCTTTTGAGTAGCTGGGACTACAAGCTCGCACCACCACACCCATCTAATTTTT CTCTTGCCTCAGTCTTTTGAGTAGCTGGGACTGCAAGCTCGCACCACCACACCCATCTAATTTTT A G NFIA Ensembl:ENSG00000162599 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1490851077 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11053508 RMVar_hsa_circ_112289,RMVar_hsa_circ_133391,RMVar_hsa_circ_297271,RMVar_hsa_circ_133393,RMVar_hsa_circ_373526,RMVar_hsa_circ_341815,RMVar_hsa_circ_357209,RMVar_hsa_circ_374796,RMVar_hsa_circ_354102,RMVar_hsa_circ_7738,RMVar_hsa_circ_293382,RMVar_hsa_circ_133397,RMVar_hsa_circ_133403 13271 RMVar_ID_13271 Human_SNP_ID_15572056 A-to-I Human chr1 + 61267357 61267357 61267357 ATGGTGAAACCCTGTCTCTACCAAAAAACACAAAAATTAGCTGGGCGTGGTGGCAGCACCTGTAA ATGGTGAAACCCTGTCTCTACCAAAAAACACAGAAATTAGCTGGGCGTGGTGGCAGCACCTGTAA A G NFIA Ensembl:ENSG00000162599 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs965777182 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112289,RMVar_hsa_circ_133391,RMVar_hsa_circ_297271,RMVar_hsa_circ_133393,RMVar_hsa_circ_373526,RMVar_hsa_circ_341815,RMVar_hsa_circ_357209,RMVar_hsa_circ_374796,RMVar_hsa_circ_354102,RMVar_hsa_circ_7738,RMVar_hsa_circ_293382,RMVar_hsa_circ_133397 13272 RMVar_ID_13272 Human_SNP_ID_15670038 A-to-I Human chr1 - 61686836 61686836 61686836 TCATTGCAGCCTCGAATTCCTGGGTTCAAACAATCTTCCTGCCTCAGCCTCCCATCCAGTATGGG TCATTGCAGCCTCGAATTCCTGGGTTCAAACAGTCTTCCTGCCTCAGCCTCCCATCCAGTATGGG T C TM2D1 Ensembl:ENSG00000162604 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs997129853 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_78486,Human_Splice_Rec_78487,Human_Splice_Rec_78498,Human_Splice_Rec_78499 RMVar_hsa_circ_125091,RMVar_hsa_circ_72168,RMVar_hsa_circ_334987,RMVar_hsa_circ_133424,RMVar_hsa_circ_353610,RMVar_hsa_circ_276262,RMVar_hsa_circ_71752,RMVar_hsa_circ_133425 13273 RMVar_ID_13273 Human_SNP_ID_15670606 A-to-I Human chr1 - 61689399 61689399 61689399 TGATTGTAGTACTACACTCTAGCATGAGCAACAGAGTGAGACCCTGTCTCAAAAAATAATAATAA TGATTGTAGTACTACACTCTAGCATGAGCAACGGAGTGAGACCCTGTCTCAAAAAATAATAATAA T C TM2D1 Ensembl:ENSG00000162604 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335135320 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125091,RMVar_hsa_circ_72168,RMVar_hsa_circ_334987,RMVar_hsa_circ_133424,RMVar_hsa_circ_353610,RMVar_hsa_circ_276262,RMVar_hsa_circ_71752,RMVar_hsa_circ_133425 13274 RMVar_ID_13274 Human_SNP_ID_15670607 A-to-I Human chr1 - 61689402 61689402 61689402 CTGTGATTGTAGTACTACACTCTAGCATGAGCAACAGAGTGAGACCCTGTCTCAAAAAATAATAA CTGTGATTGTAGTACTACACTCTAGCATGAGCCACAGAGTGAGACCCTGTCTCAAAAAATAATAA T G TM2D1 Ensembl:ENSG00000162604 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1411232860 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125091,RMVar_hsa_circ_72168,RMVar_hsa_circ_334987,RMVar_hsa_circ_133424,RMVar_hsa_circ_353610,RMVar_hsa_circ_276262,RMVar_hsa_circ_71752,RMVar_hsa_circ_133425 13275 RMVar_ID_13275 Human_SNP_ID_15670619 A-to-I Human chr1 - 61689435 61689435 61689435 AGCCTGAGAGATCGATCAAGGTTGCAGAGTGAACTGTGATTGTAGTACTACACTCTAGCATGAGC AGCCTGAGAGATCGATCAAGGTTGCAGAGTGATCTGTGATTGTAGTACTACACTCTAGCATGAGC T A TM2D1 Ensembl:ENSG00000162604 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs914372847 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11060194 RMVar_hsa_circ_125091,RMVar_hsa_circ_72168,RMVar_hsa_circ_334987,RMVar_hsa_circ_133424,RMVar_hsa_circ_353610,RMVar_hsa_circ_276262,RMVar_hsa_circ_71752,RMVar_hsa_circ_133425 13276 RMVar_ID_13276 Human_SNP_ID_15670632 A-to-I Human chr1 - 61689494 61689494 61689494 GTGGTGGTGCATGCCTGTAGTTCCAACTGCTCAGGAGGCTGAGGTTGGAGGATCACTTGAGCCTG GTGGTGGTGCATGCCTGTAGTTCCAACTGCTCTGGAGGCTGAGGTTGGAGGATCACTTGAGCCTG T A TM2D1 Ensembl:ENSG00000162604 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947841449 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125091,RMVar_hsa_circ_72168,RMVar_hsa_circ_334987,RMVar_hsa_circ_133424,RMVar_hsa_circ_353610,RMVar_hsa_circ_276262,RMVar_hsa_circ_71752,RMVar_hsa_circ_133425 13277 RMVar_ID_13277 Human_SNP_ID_15670633 A-to-I Human chr1 - 61689494 61689494 61689494 GTGGTGGTGCATGCCTGTAGTTCCAACTGCTCAGGAGGCTGAGGTTGGAGGATCACTTGAGCCTG GTGGTGGTGCATGCCTGTAGTTCCAACTGCTCGGGAGGCTGAGGTTGGAGGATCACTTGAGCCTG T C TM2D1 Ensembl:ENSG00000162604 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947841449 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125091,RMVar_hsa_circ_72168,RMVar_hsa_circ_334987,RMVar_hsa_circ_133424,RMVar_hsa_circ_353610,RMVar_hsa_circ_276262,RMVar_hsa_circ_71752,RMVar_hsa_circ_133425 13278 RMVar_ID_13278 Human_SNP_ID_15670634 A-to-I Human chr1 - 61689501 61689501 61689501 GCCAGGTGTGGTGGTGCATGCCTGTAGTTCCAACTGCTCAGGAGGCTGAGGTTGGAGGATCACTT GCCAGGTGTGGTGGTGCATGCCTGTAGTTCCAGCTGCTCAGGAGGCTGAGGTTGGAGGATCACTT T C TM2D1 Ensembl:ENSG00000162604 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs536242504 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125091,RMVar_hsa_circ_72168,RMVar_hsa_circ_334987,RMVar_hsa_circ_133424,RMVar_hsa_circ_353610,RMVar_hsa_circ_276262,RMVar_hsa_circ_71752,RMVar_hsa_circ_133425 13279 RMVar_ID_13279 Human_SNP_ID_15670827 A-to-I Human chr1 - 61690438 61690438 61690438 TTTTTTTTTTTTTTGAGACTGAGTCTTGCCCTATTGCTCAGGCTGGAGTACAGTGGCGCAATCTC TTTTTTTTTTTTTTGAGACTGAGTCTTGCCCTGTTGCTCAGGCTGGAGTACAGTGGCGCAATCTC T C TM2D1 Ensembl:ENSG00000162604 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1332746561 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5848680 RMVar_hsa_circ_125091,RMVar_hsa_circ_72168,RMVar_hsa_circ_334987,RMVar_hsa_circ_133424,RMVar_hsa_circ_353610,RMVar_hsa_circ_276262,RMVar_hsa_circ_71752,RMVar_hsa_circ_133425 13280 RMVar_ID_13280 Human_SNP_ID_15671680 A-to-I Human chr1 - 61693064 61693064 61693064 CCTGGCTAATTTTTGTATATTCTGAAGAGACAAGGTTTCCCCATGTTGCCCAGGCTGGTCTCCTG CCTGGCTAATTTTTGTATATTCTGAAGAGACAGGGTTTCCCCATGTTGCCCAGGCTGGTCTCCTG T C TM2D1 Ensembl:ENSG00000162604 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1243972432 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8972500,Human_RBP_ID_11060347 RMVar_hsa_circ_125091,RMVar_hsa_circ_72168,RMVar_hsa_circ_334987,RMVar_hsa_circ_133424,RMVar_hsa_circ_353610,RMVar_hsa_circ_276262,RMVar_hsa_circ_71752,RMVar_hsa_circ_133425 13281 RMVar_ID_13281 Human_SNP_ID_15671681 A-to-I Human chr1 - 61693064 61693064 61693064 CCTGGCTAATTTTTGTATATTCTGAAGAGACAAGGTTTCCCCATGTTGCCCAGGCTGGTCTCCTG CCTGGCTAATTTTTGTATATTCTGAAGAGACACGGTTTCCCCATGTTGCCCAGGCTGGTCTCCTG T G TM2D1 Ensembl:ENSG00000162604 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1243972432 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8972500,Human_RBP_ID_11060347 RMVar_hsa_circ_125091,RMVar_hsa_circ_72168,RMVar_hsa_circ_334987,RMVar_hsa_circ_133424,RMVar_hsa_circ_353610,RMVar_hsa_circ_276262,RMVar_hsa_circ_71752,RMVar_hsa_circ_133425 13282 RMVar_ID_13282 Human_SNP_ID_15672532 A-to-I Human chr1 - 61696896 61696896 61696896 AAAAAAATTTAGGCCAGGTGTGATGGCCTGTAATCGAAGCATTTTGGGAGGCCAAGGCAGGAAGA AAAAAAATTTAGGCCAGGTGTGATGGCCTGTACTCGAAGCATTTTGGGAGGCCAAGGCAGGAAGA T G TM2D1 Ensembl:ENSG00000162604 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1184094442 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37450,RMVar_hsa_circ_125091,RMVar_hsa_circ_72168,RMVar_hsa_circ_133424,RMVar_hsa_circ_353610,RMVar_hsa_circ_276262,RMVar_hsa_circ_71752,RMVar_hsa_circ_274453,RMVar_hsa_circ_347062,RMVar_hsa_circ_133426,RMVar_hsa_circ_133427 13283 RMVar_ID_13283 Human_SNP_ID_15674066 A-to-I Human chr1 - 61703049 61703049 61703049 CAGGCAGGAGTGCAATGGCGTGATCTTGGCTCACTGCAACCTCCGCTTCCCAGGTTCAAGCGATT CAGGCAGGAGTGCAATGGCGTGATCTTGGCTCCCTGCAACCTCCGCTTCCCAGGTTCAAGCGATT T G TM2D1 Ensembl:ENSG00000162604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs573595746 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37450,RMVar_hsa_circ_125091,RMVar_hsa_circ_133424,RMVar_hsa_circ_353610,RMVar_hsa_circ_276262,RMVar_hsa_circ_71752,RMVar_hsa_circ_274453,RMVar_hsa_circ_133428,RMVar_hsa_circ_109298,RMVar_hsa_circ_133427,RMVar_hsa_circ_321499,RMVar_hsa_circ_342379,RMVar_hsa_circ_133429 13284 RMVar_ID_13284 Human_SNP_ID_15675078 A-to-I Human chr1 - 61707092 61707092 61707092 TGCCCCAAAGCTCGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGCCCAGGC TGCCCCAAAGCTCGGCTAATTTTTGTATTTTTGGTAGAGATGGGGTTTCACCATGTTGCCCAGGC T C TM2D1 Ensembl:ENSG00000162604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1296906278 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37450,RMVar_hsa_circ_125091,RMVar_hsa_circ_133424,RMVar_hsa_circ_353610,RMVar_hsa_circ_276262,RMVar_hsa_circ_71752,RMVar_hsa_circ_274453,RMVar_hsa_circ_133428,RMVar_hsa_circ_109298,RMVar_hsa_circ_133427,RMVar_hsa_circ_321499,RMVar_hsa_circ_342379,RMVar_hsa_circ_133429,RMVar_hsa_circ_133430,RMVar_hsa_circ_91742 13285 RMVar_ID_13285 Human_SNP_ID_15675080 A-to-I Human chr1 - 61707107 61707107 61707107 GGGACTAGAGGTGCATGCCCCAAAGCTCGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCA GGGACTAGAGGTGCATGCCCCAAAGCTCGGCTGATTTTTGTATTTTTAGTAGAGATGGGGTTTCA T C TM2D1 Ensembl:ENSG00000162604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1371968757 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37450,RMVar_hsa_circ_125091,RMVar_hsa_circ_133424,RMVar_hsa_circ_353610,RMVar_hsa_circ_276262,RMVar_hsa_circ_71752,RMVar_hsa_circ_274453,RMVar_hsa_circ_133428,RMVar_hsa_circ_109298,RMVar_hsa_circ_133427,RMVar_hsa_circ_321499,RMVar_hsa_circ_342379,RMVar_hsa_circ_133429,RMVar_hsa_circ_133430,RMVar_hsa_circ_91742 13286 RMVar_ID_13286 Human_SNP_ID_15676081 A-to-I Human chr1 - 61711120 61711120 61711120 TTGCCCAGGCTGGTGTCGCACTCCAAACCTCAAGTGATCCATCTGCCTCGGCCTCTCAAAGTGCT TTGCCCAGGCTGGTGTCGCACTCCAAACCTCACGTGATCCATCTGCCTCGGCCTCTCAAAGTGCT T G TM2D1 Ensembl:ENSG00000162604 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1010042389 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8316173 RMVar_hsa_circ_37450,RMVar_hsa_circ_353610,RMVar_hsa_circ_133428,RMVar_hsa_circ_109298,RMVar_hsa_circ_342379,RMVar_hsa_circ_133429,RMVar_hsa_circ_133431,RMVar_hsa_circ_304829 13287 RMVar_ID_13287 Human_SNP_ID_15676413 A-to-I Human chr1 - 61712551 61712551 61712551 CAAAAATTAATTGGACATGGTAGCAGGTGCCTATAATCCCAGCTACTGGAGAGGCTGAGACATGA CAAAAATTAATTGGACATGGTAGCAGGTGCCTGTAATCCCAGCTACTGGAGAGGCTGAGACATGA T C TM2D1 Ensembl:ENSG00000162604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1391196594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11060920 RMVar_hsa_circ_37450,RMVar_hsa_circ_353610,RMVar_hsa_circ_133428,RMVar_hsa_circ_109298,RMVar_hsa_circ_342379,RMVar_hsa_circ_133429,RMVar_hsa_circ_133431,RMVar_hsa_circ_304829 13288 RMVar_ID_13288 Human_SNP_ID_15676519 A-to-I Human chr1 - 61713007 61713007 61713007 TGCCACCACACCCCACTGATTTTTGTCTTTTTAGTAGAGACAGGGTTTCACCATGTTGGTCAGGT TGCCACCACACCCCACTGATTTTTGTCTTTTTGGTAGAGACAGGGTTTCACCATGTTGGTCAGGT T C TM2D1 Ensembl:ENSG00000162604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1011077298 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11218159 RMVar_hsa_circ_37450,RMVar_hsa_circ_353610,RMVar_hsa_circ_133428,RMVar_hsa_circ_109298,RMVar_hsa_circ_342379,RMVar_hsa_circ_133429,RMVar_hsa_circ_133431,RMVar_hsa_circ_304829 13289 RMVar_ID_13289 Human_SNP_ID_15676520 A-to-I Human chr1 - 61713007 61713007 61713007 TGCCACCACACCCCACTGATTTTTGTCTTTTTAGTAGAGACAGGGTTTCACCATGTTGGTCAGGT TGCCACCACACCCCACTGATTTTTGTCTTTTTCGTAGAGACAGGGTTTCACCATGTTGGTCAGGT T G TM2D1 Ensembl:ENSG00000162604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1011077298 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11218159 RMVar_hsa_circ_37450,RMVar_hsa_circ_353610,RMVar_hsa_circ_133428,RMVar_hsa_circ_109298,RMVar_hsa_circ_342379,RMVar_hsa_circ_133429,RMVar_hsa_circ_133431,RMVar_hsa_circ_304829 13290 RMVar_ID_13290 Human_SNP_ID_15676601 A-to-I Human chr1 - 61713256 61713256 61713256 CCAGACTGGTCTTGAACTCCTGGCTGCAAGCAATTCACCTGCCTCGGCCTCCCAAAGTGCTGGGA CCAGACTGGTCTTGAACTCCTGGCTGCAAGCAGTTCACCTGCCTCGGCCTCCCAAAGTGCTGGGA T C TM2D1 Ensembl:ENSG00000162604 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559052601 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11060932,Human_RBP_ID_24767981 RMVar_hsa_circ_37450,RMVar_hsa_circ_353610,RMVar_hsa_circ_133428,RMVar_hsa_circ_109298,RMVar_hsa_circ_342379,RMVar_hsa_circ_133429,RMVar_hsa_circ_133431,RMVar_hsa_circ_304829 13291 RMVar_ID_13291 Human_SNP_ID_15677003 A-to-I Human chr1 - 61714458 61714458 61714458 CAGCTCACTGAAACCTCCGCTTCCCGGGTCCAAGCAATTTTCCTGCCTCAGCCTCCTGACTAGCT CAGCTCACTGAAACCTCCGCTTCCCGGGTCCAGGCAATTTTCCTGCCTCAGCCTCCTGACTAGCT T C TM2D1 Ensembl:ENSG00000162604 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1314640292 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37450,RMVar_hsa_circ_353610,RMVar_hsa_circ_133428,RMVar_hsa_circ_109298,RMVar_hsa_circ_342379,RMVar_hsa_circ_133429,RMVar_hsa_circ_133431,RMVar_hsa_circ_304829 13292 RMVar_ID_13292 Human_SNP_ID_15677019 A-to-I Human chr1 - 61714535 61714534 61714536 CGAAAGAAAGGGCTCTTTAGTTTTTTTTGGACAGAGTCTTGCTGTGTCACCCAGGCTGGAGTGCA CGAAAGAAAGGGCTCTTTAGTTTTTTTTGGA__GAGTCTTGCTGTGTCACCCAGGCTGGAGTGCA CTG C TM2D1 Ensembl:ENSG00000162604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1316534166 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_37450,RMVar_hsa_circ_353610,RMVar_hsa_circ_133428,RMVar_hsa_circ_109298,RMVar_hsa_circ_342379,RMVar_hsa_circ_133429,RMVar_hsa_circ_133431,RMVar_hsa_circ_304829 13293 RMVar_ID_13293 Human_SNP_ID_15677258 A-to-I Human chr1 - 61715456 61715456 61715456 TTTAGTAGAGACGGGGTTTTACCATGTTGGCCAGGCTGGTCTCGAATTCCTGGACTCAAGTGATC TTTAGTAGAGACGGGGTTTTACCATGTTGGCCGGGCTGGTCTCGAATTCCTGGACTCAAGTGATC T C TM2D1 Ensembl:ENSG00000162604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1260226447 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37450,RMVar_hsa_circ_353610,RMVar_hsa_circ_133428,RMVar_hsa_circ_109298,RMVar_hsa_circ_342379,RMVar_hsa_circ_133429,RMVar_hsa_circ_133431,RMVar_hsa_circ_304829 13294 RMVar_ID_13294 Human_SNP_ID_15677276 A-to-I Human chr1 - 61715548 61715548 61715548 TGCCTCTCGGGTTCAAGCAATTCTTGTGCCTCAGCCTCTTCAGTAGCTGGGACTACGGATGCAGG TGCCTCTCGGGTTCAAGCAATTCTTGTGCCTCCGCCTCTTCAGTAGCTGGGACTACGGATGCAGG T G TM2D1 Ensembl:ENSG00000162604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs970149160 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37450,RMVar_hsa_circ_353610,RMVar_hsa_circ_133428,RMVar_hsa_circ_109298,RMVar_hsa_circ_342379,RMVar_hsa_circ_133429,RMVar_hsa_circ_133431,RMVar_hsa_circ_304829 13295 RMVar_ID_13295 Human_SNP_ID_15677551 A-to-I Human chr1 - 61716280 61716280 61716280 AGGCCTTACTCTGTCGCCCAGGCTGTAGTGCAATGGCAGGATCGTAGCTTACTGCAGCCTGGATC AGGCCTTACTCTGTCGCCCAGGCTGTAGTGCATTGGCAGGATCGTAGCTTACTGCAGCCTGGATC T A TM2D1 Ensembl:ENSG00000162604 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1178803919 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11060984,Human_RBP_ID_17557915 RMVar_hsa_circ_37450,RMVar_hsa_circ_353610,RMVar_hsa_circ_133428,RMVar_hsa_circ_109298,RMVar_hsa_circ_342379,RMVar_hsa_circ_133429,RMVar_hsa_circ_133431,RMVar_hsa_circ_304829 13296 RMVar_ID_13296 Human_SNP_ID_15677552 A-to-I Human chr1 - 61716280 61716280 61716280 AGGCCTTACTCTGTCGCCCAGGCTGTAGTGCAATGGCAGGATCGTAGCTTACTGCAGCCTGGATC AGGCCTTACTCTGTCGCCCAGGCTGTAGTGCAGTGGCAGGATCGTAGCTTACTGCAGCCTGGATC T C TM2D1 Ensembl:ENSG00000162604 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1178803919 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11060984,Human_RBP_ID_17557915 RMVar_hsa_circ_37450,RMVar_hsa_circ_353610,RMVar_hsa_circ_133428,RMVar_hsa_circ_109298,RMVar_hsa_circ_342379,RMVar_hsa_circ_133429,RMVar_hsa_circ_133431,RMVar_hsa_circ_304829 13297 RMVar_ID_13297 Human_SNP_ID_15678052 A-to-I Human chr1 - 61717711 61717711 61717711 TATACCAGGTGTGGTGGTGGTGTGTGCCTGTAATCCTGGCTATTTGGTAGTCTGAGGCTGGAGGA TATACCAGGTGTGGTGGTGGTGTGTGCCTGTAGTCCTGGCTATTTGGTAGTCTGAGGCTGGAGGA T C TM2D1 Ensembl:ENSG00000162604 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs903145855 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37450,RMVar_hsa_circ_353610,RMVar_hsa_circ_133428,RMVar_hsa_circ_109298,RMVar_hsa_circ_342379,RMVar_hsa_circ_133429,RMVar_hsa_circ_133431,RMVar_hsa_circ_304829 13298 RMVar_ID_13298 Human_SNP_ID_15678138 A-to-I Human chr1 - 61718061 61718061 61718061 CACTTGCCTCGGCCTCCGAAAGTGTTGGAATTACAGTTGTGAGCCACCACACCTGGCGTTTTTTG CACTTGCCTCGGCCTCCGAAAGTGTTGGAATTGCAGTTGTGAGCCACCACACCTGGCGTTTTTTG T C TM2D1 Ensembl:ENSG00000162604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs547054462 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37450,RMVar_hsa_circ_353610,RMVar_hsa_circ_133428,RMVar_hsa_circ_109298,RMVar_hsa_circ_342379,RMVar_hsa_circ_133429,RMVar_hsa_circ_133431,RMVar_hsa_circ_304829 13299 RMVar_ID_13299 Human_SNP_ID_15678139 A-to-I Human chr1 - 61718073 61718068 61718073 GCTCAAGCAATCCACTTGCCTCGGCCTCCGAAAGTGTTGGAATTACAGTTGTGAGCCACCACACC GCTCAAGCAATCCACTTGCCTCGGCCTCCGAA_____TGGAATTACAGTTGTGAGCCACCACACC AACACT A TM2D1 Ensembl:ENSG00000162604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1307124904 Functional Loss DEL dbSNP153 33..37 33 - - - RMVar_hsa_circ_37450,RMVar_hsa_circ_353610,RMVar_hsa_circ_133428,RMVar_hsa_circ_109298,RMVar_hsa_circ_342379,RMVar_hsa_circ_133429,RMVar_hsa_circ_133431,RMVar_hsa_circ_304829 13300 RMVar_ID_13300 Human_SNP_ID_15678147 A-to-I Human chr1 - 61718092 61718092 61718092 GCTGGTTTCTAACTCCTGAGCTCAAGCAATCCACTTGCCTCGGCCTCCGAAAGTGTTGGAATTAC GCTGGTTTCTAACTCCTGAGCTCAAGCAATCCGCTTGCCTCGGCCTCCGAAAGTGTTGGAATTAC T C TM2D1 Ensembl:ENSG00000162604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1004377205 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37450,RMVar_hsa_circ_353610,RMVar_hsa_circ_133428,RMVar_hsa_circ_109298,RMVar_hsa_circ_342379,RMVar_hsa_circ_133429,RMVar_hsa_circ_133431,RMVar_hsa_circ_304829 13301 RMVar_ID_13301 Human_SNP_ID_15678148 A-to-I Human chr1 - 61718097 61718097 61718097 CCCAAGCTGGTTTCTAACTCCTGAGCTCAAGCAATCCACTTGCCTCGGCCTCCGAAAGTGTTGGA CCCAAGCTGGTTTCTAACTCCTGAGCTCAAGCGATCCACTTGCCTCGGCCTCCGAAAGTGTTGGA T C TM2D1 Ensembl:ENSG00000162604 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1313936257 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37450,RMVar_hsa_circ_353610,RMVar_hsa_circ_133428,RMVar_hsa_circ_109298,RMVar_hsa_circ_342379,RMVar_hsa_circ_133429,RMVar_hsa_circ_133431,RMVar_hsa_circ_304829 13302 RMVar_ID_13302 Human_SNP_ID_15678393 A-to-I Human chr1 - 61719292 61719292 61719292 TAATCCCAGCACTTTGGGAGGCTTAGGTGGGCAGATCACTTGAACCCAGGAGTTCTAGACCAGCC TAATCCCAGCACTTTGGGAGGCTTAGGTGGGCCGATCACTTGAACCCAGGAGTTCTAGACCAGCC T G TM2D1 Ensembl:ENSG00000162604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1470276532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11061081 RMVar_hsa_circ_37450,RMVar_hsa_circ_353610,RMVar_hsa_circ_133428,RMVar_hsa_circ_109298,RMVar_hsa_circ_342379,RMVar_hsa_circ_133429,RMVar_hsa_circ_133431,RMVar_hsa_circ_304829 13303 RMVar_ID_13303 Human_SNP_ID_15678698 A-to-I Human chr1 - 61720521 61720521 61720521 AGTGTTCTGTCAGCCCGGGTGAGGTGGCTCACACCTATAATCCCATCACTTTGGGAGGCTGAGGT AGTGTTCTGTCAGCCCGGGTGAGGTGGCTCACGCCTATAATCCCATCACTTTGGGAGGCTGAGGT T C TM2D1 Ensembl:ENSG00000162604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1301642415 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37450,RMVar_hsa_circ_353610,RMVar_hsa_circ_133428,RMVar_hsa_circ_109298,RMVar_hsa_circ_342379,RMVar_hsa_circ_133429,RMVar_hsa_circ_133431,RMVar_hsa_circ_304829 13304 RMVar_ID_13304 Human_SNP_ID_15678816 A-to-I Human chr1 - 61721101 61721101 61721101 TCAGCCTCTTGAGTAGCTGGGACTACAGGTACATGCCACTACACCTGGCTAATTTTTTGTATTTT TCAGCCTCTTGAGTAGCTGGGACTACAGGTACGTGCCACTACACCTGGCTAATTTTTTGTATTTT T C TM2D1 Ensembl:ENSG00000162604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1052851568 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37450,RMVar_hsa_circ_353610,RMVar_hsa_circ_133428,RMVar_hsa_circ_109298,RMVar_hsa_circ_342379,RMVar_hsa_circ_133429,RMVar_hsa_circ_133431,RMVar_hsa_circ_304829 13305 RMVar_ID_13305 Human_SNP_ID_15678841 A-to-I Human chr1 - 61721200 61721200 61721200 TTAAGACAGGATCTCACTCTGTCACCCAGGCTAGACTGCAGTGGCACCGTCTTAGCTCACTGCAA TTAAGACAGGATCTCACTCTGTCACCCAGGCTTGACTGCAGTGGCACCGTCTTAGCTCACTGCAA T A TM2D1 Ensembl:ENSG00000162604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs889246661 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11061119 RMVar_hsa_circ_37450,RMVar_hsa_circ_353610,RMVar_hsa_circ_133428,RMVar_hsa_circ_109298,RMVar_hsa_circ_342379,RMVar_hsa_circ_133429,RMVar_hsa_circ_133431,RMVar_hsa_circ_304829 13306 RMVar_ID_13306 Human_SNP_ID_15678842 A-to-I Human chr1 - 61721200 61721200 61721200 TTAAGACAGGATCTCACTCTGTCACCCAGGCTAGACTGCAGTGGCACCGTCTTAGCTCACTGCAA TTAAGACAGGATCTCACTCTGTCACCCAGGCTGGACTGCAGTGGCACCGTCTTAGCTCACTGCAA T C TM2D1 Ensembl:ENSG00000162604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs889246661 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11061119 RMVar_hsa_circ_37450,RMVar_hsa_circ_353610,RMVar_hsa_circ_133428,RMVar_hsa_circ_109298,RMVar_hsa_circ_342379,RMVar_hsa_circ_133429,RMVar_hsa_circ_133431,RMVar_hsa_circ_304829 13307 RMVar_ID_13307 Human_SNP_ID_15679180 A-to-I Human chr1 - 61722507 61722507 61722507 AAAATTAGCCAGGTGCAGTGATGGGCACCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGATA AAAATTAGCCAGGTGCAGTGATGGGCACCTGTTATCCCAGCTACTCGGGAGGCTGAGGCAGGATA T A TM2D1 Ensembl:ENSG00000162604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1557542190 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37450,RMVar_hsa_circ_353610,RMVar_hsa_circ_133428,RMVar_hsa_circ_109298,RMVar_hsa_circ_342379,RMVar_hsa_circ_133429,RMVar_hsa_circ_133431,RMVar_hsa_circ_304829 13308 RMVar_ID_13308 Human_SNP_ID_15686434 A-to-I Human chr1 + 61750513 61750513 61750513 GCTGGAGTGCAATGGTGTGGTCTCGGCTCACCACAACCTCTGCCTCCCGGGTTCGGGTGATTCTC GCTGGAGTGCAATGGTGTGGTCTCGGCTCACCGCAACCTCTGCCTCCCGGGTTCGGGTGATTCTC A G PATJ Ensembl:ENSG00000132849 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1176675901 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11061332 RMVar_hsa_circ_77691,RMVar_hsa_circ_133432 13309 RMVar_ID_13309 Human_SNP_ID_15696990 A-to-I Human chr1 + 61794379 61794379 61794379 GTCACCCAGGCTGGCCTCAAAGTCCTGGGCTCAGGTGATCCTCCCCCCTCAGCCTCCCAAAGCGC GTCACCCAGGCTGGCCTCAAAGTCCTGGGCTCCGGTGATCCTCCCCCCTCAGCCTCCCAAAGCGC A C PATJ Ensembl:ENSG00000132849 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978596188 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11061549 RMVar_hsa_circ_4450,RMVar_hsa_circ_58891,RMVar_hsa_circ_70315,RMVar_hsa_circ_54655,RMVar_hsa_circ_41057,RMVar_hsa_circ_14655,RMVar_hsa_circ_126201,RMVar_hsa_circ_133437,RMVar_hsa_circ_94069,RMVar_hsa_circ_365439,RMVar_hsa_circ_21192,RMVar_hsa_circ_50248,RMVar_hsa_circ_133438,RMVar_hsa_circ_378478,RMVar_hsa_circ_98665,RMVar_hsa_circ_133439,RMVar_hsa_circ_360998,RMVar_hsa_circ_60032,RMVar_hsa_circ_68987,RMVar_hsa_circ_354458,RMVar_hsa_circ_44701,RMVar_hsa_circ_73717,RMVar_hsa_circ_27713,RMVar_hsa_circ_38453,RMVar_hsa_circ_307597,RMVar_hsa_circ_355070,RMVar_hsa_circ_25145,RMVar_hsa_circ_336337,RMVar_hsa_circ_278137,RMVar_hsa_circ_71017 13310 RMVar_ID_13310 Human_SNP_ID_15705813 A-to-I Human chr1 + 61828639 61828639 61828639 GTCTCAAACTCCTGGACTCAAGCAATCCTCCCACCTCAACCCCCCAAAATGCTGGGTTTATAGGT GTCTCAAACTCCTGGACTCAAGCAATCCTCCCGCCTCAACCCCCCAAAATGCTGGGTTTATAGGT A G PATJ Ensembl:ENSG00000132849 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1484775983 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4450,RMVar_hsa_circ_70315,RMVar_hsa_circ_14157,RMVar_hsa_circ_14655,RMVar_hsa_circ_126201,RMVar_hsa_circ_133437,RMVar_hsa_circ_94069,RMVar_hsa_circ_21192,RMVar_hsa_circ_133438,RMVar_hsa_circ_98665,RMVar_hsa_circ_133439,RMVar_hsa_circ_354458,RMVar_hsa_circ_73717,RMVar_hsa_circ_38453,RMVar_hsa_circ_25145,RMVar_hsa_circ_62313,RMVar_hsa_circ_71017,RMVar_hsa_circ_112720,RMVar_hsa_circ_133442,RMVar_hsa_circ_102587,RMVar_hsa_circ_118613,RMVar_hsa_circ_133443,RMVar_hsa_circ_133444,RMVar_hsa_circ_271260,RMVar_hsa_circ_354332,RMVar_hsa_circ_85296,RMVar_hsa_circ_59875,RMVar_hsa_circ_117492,RMVar_hsa_circ_350856,RMVar_hsa_circ_359200,RMVar_hsa_circ_133446,RMVar_hsa_circ_133447,RMVar_hsa_circ_133445,RMVar_hsa_circ_364081,RMVar_hsa_circ_354346,RMVar_hsa_circ_357449,RMVar_hsa_circ_352956,RMVar_hsa_circ_328279,RMVar_hsa_circ_333287,RMVar_hsa_circ_315153,RMVar_hsa_circ_69733,RMVar_hsa_circ_72677,RMVar_hsa_circ_61175,RMVar_hsa_circ_133448,RMVar_hsa_circ_59459,RMVar_hsa_circ_133449 13311 RMVar_ID_13311 Human_SNP_ID_15705815 A-to-I Human chr1 + 61828644 61828644 61828644 AAACTCCTGGACTCAAGCAATCCTCCCACCTCAACCCCCCAAAATGCTGGGTTTATAGGTGTGAG AAACTCCTGGACTCAAGCAATCCTCCCACCTCGACCCCCCAAAATGCTGGGTTTATAGGTGTGAG A G PATJ Ensembl:ENSG00000132849 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs928375896 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4450,RMVar_hsa_circ_70315,RMVar_hsa_circ_14157,RMVar_hsa_circ_14655,RMVar_hsa_circ_126201,RMVar_hsa_circ_133437,RMVar_hsa_circ_94069,RMVar_hsa_circ_21192,RMVar_hsa_circ_133438,RMVar_hsa_circ_98665,RMVar_hsa_circ_133439,RMVar_hsa_circ_354458,RMVar_hsa_circ_73717,RMVar_hsa_circ_38453,RMVar_hsa_circ_25145,RMVar_hsa_circ_62313,RMVar_hsa_circ_71017,RMVar_hsa_circ_112720,RMVar_hsa_circ_133442,RMVar_hsa_circ_102587,RMVar_hsa_circ_118613,RMVar_hsa_circ_133443,RMVar_hsa_circ_133444,RMVar_hsa_circ_271260,RMVar_hsa_circ_354332,RMVar_hsa_circ_85296,RMVar_hsa_circ_59875,RMVar_hsa_circ_117492,RMVar_hsa_circ_350856,RMVar_hsa_circ_359200,RMVar_hsa_circ_133446,RMVar_hsa_circ_133447,RMVar_hsa_circ_133445,RMVar_hsa_circ_364081,RMVar_hsa_circ_354346,RMVar_hsa_circ_357449,RMVar_hsa_circ_352956,RMVar_hsa_circ_328279,RMVar_hsa_circ_333287,RMVar_hsa_circ_315153,RMVar_hsa_circ_69733,RMVar_hsa_circ_72677,RMVar_hsa_circ_61175,RMVar_hsa_circ_133448,RMVar_hsa_circ_59459,RMVar_hsa_circ_133449 13312 RMVar_ID_13312 Human_SNP_ID_15728078 A-to-I Human chr1 + 61924237 61924237 61924237 CAAAAATACAAAAATTAGCCAGGTGTGGTGGTACGAGCTTGTAATCCCAGCTACTTGGGAGGCTG CAAAAATACAAAAATTAGCCAGGTGTGGTGGTGCGAGCTTGTAATCCCAGCTACTTGGGAGGCTG A G PATJ Ensembl:ENSG00000132849 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1317247684 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14157,RMVar_hsa_circ_21192,RMVar_hsa_circ_25145,RMVar_hsa_circ_112720,RMVar_hsa_circ_133442,RMVar_hsa_circ_118613,RMVar_hsa_circ_133444,RMVar_hsa_circ_53754,RMVar_hsa_circ_59875,RMVar_hsa_circ_350856,RMVar_hsa_circ_354346,RMVar_hsa_circ_357449,RMVar_hsa_circ_69733,RMVar_hsa_circ_72677,RMVar_hsa_circ_61175,RMVar_hsa_circ_50518,RMVar_hsa_circ_66373,RMVar_hsa_circ_351324,RMVar_hsa_circ_363251,RMVar_hsa_circ_360641,RMVar_hsa_circ_333718,RMVar_hsa_circ_104858,RMVar_hsa_circ_58828,RMVar_hsa_circ_46047,RMVar_hsa_circ_133450,RMVar_hsa_circ_54336,RMVar_hsa_circ_351626,RMVar_hsa_circ_57395,RMVar_hsa_circ_67356,RMVar_hsa_circ_133456,RMVar_hsa_circ_53021,RMVar_hsa_circ_273050 13313 RMVar_ID_13313 Human_SNP_ID_15729705 A-to-I Human chr1 + 61931643 61931643 61931643 AAAATTAACTGGGTATGGTGGTGAACATCTATAGTCCCACCCACTTGGAAGGCTGAGGTGAGAGG AAAATTAACTGGGTATGGTGGTGAACATCTATCGTCCCACCCACTTGGAAGGCTGAGGTGAGAGG A C PATJ Ensembl:ENSG00000132849 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs774674113 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21192,RMVar_hsa_circ_112720,RMVar_hsa_circ_133442,RMVar_hsa_circ_53754,RMVar_hsa_circ_59875,RMVar_hsa_circ_350856,RMVar_hsa_circ_354346,RMVar_hsa_circ_69733,RMVar_hsa_circ_72677,RMVar_hsa_circ_61175,RMVar_hsa_circ_50518,RMVar_hsa_circ_351324,RMVar_hsa_circ_363251,RMVar_hsa_circ_360641,RMVar_hsa_circ_104858,RMVar_hsa_circ_58828,RMVar_hsa_circ_46047,RMVar_hsa_circ_133450,RMVar_hsa_circ_54336,RMVar_hsa_circ_57395,RMVar_hsa_circ_53021,RMVar_hsa_circ_28997,RMVar_hsa_circ_84048,RMVar_hsa_circ_337095,RMVar_hsa_circ_350685,RMVar_hsa_circ_296530,RMVar_hsa_circ_63294,RMVar_hsa_circ_133458 13314 RMVar_ID_13314 Human_SNP_ID_15729951 A-to-I Human chr1 + 61932789 61932789 61932789 GGGTGTGGTGTTGCACACCTGTAGTCCCAACTAGTCGGGAGGCTGAGGCACAAGTATCACTTGAA GGGTGTGGTGTTGCACACCTGTAGTCCCAACTTGTCGGGAGGCTGAGGCACAAGTATCACTTGAA A T PATJ Ensembl:ENSG00000132849 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1455204547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_96986 RMVar_hsa_circ_21192,RMVar_hsa_circ_112720,RMVar_hsa_circ_133442,RMVar_hsa_circ_53754,RMVar_hsa_circ_59875,RMVar_hsa_circ_350856,RMVar_hsa_circ_354346,RMVar_hsa_circ_69733,RMVar_hsa_circ_72677,RMVar_hsa_circ_61175,RMVar_hsa_circ_50518,RMVar_hsa_circ_351324,RMVar_hsa_circ_363251,RMVar_hsa_circ_360641,RMVar_hsa_circ_104858,RMVar_hsa_circ_58828,RMVar_hsa_circ_46047,RMVar_hsa_circ_133450,RMVar_hsa_circ_54336,RMVar_hsa_circ_57395,RMVar_hsa_circ_53021,RMVar_hsa_circ_28997,RMVar_hsa_circ_84048,RMVar_hsa_circ_337095,RMVar_hsa_circ_350685,RMVar_hsa_circ_296530,RMVar_hsa_circ_63294,RMVar_hsa_circ_133458 13315 RMVar_ID_13315 Human_SNP_ID_15776759 A-to-I Human chr1 + 62132377 62132377 62132377 AAAAAGTAGCCGGATTGGCGGTGCACCTCTGTAATCCTGGCTGCTCAGGAGGCTGAGGCGGGAGA AAAAAGTAGCCGGATTGGCGGTGCACCTCTGTGATCCTGGCTGCTCAGGAGGCTGAGGCGGGAGA A G PATJ Ensembl:ENSG00000132849 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1051677802 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20162,RMVar_hsa_circ_133476,RMVar_hsa_circ_373305,RMVar_hsa_circ_338741,RMVar_hsa_circ_133477 13316 RMVar_ID_13316 Human_SNP_ID_15782623 A-to-I Human chr1 + 62154580 62154580 62154580 CTACTTGGGAGGCTGAGACATGAAAATCCCTTAAATCTGGGAGGCAGAGGTTGCCATGATCCCAG CTACTTGGGAGGCTGAGACATGAAAATCCCTTCAATCTGGGAGGCAGAGGTTGCCATGATCCCAG A C PATJ Ensembl:ENSG00000132849 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs546168468 Functional Loss SNV dbSNP153 33..33 33 - - - 13317 RMVar_ID_13317 Human_SNP_ID_15782624 A-to-I Human chr1 + 62154580 62154580 62154580 CTACTTGGGAGGCTGAGACATGAAAATCCCTTAAATCTGGGAGGCAGAGGTTGCCATGATCCCAG CTACTTGGGAGGCTGAGACATGAAAATCCCTTGAATCTGGGAGGCAGAGGTTGCCATGATCCCAG A G PATJ Ensembl:ENSG00000132849 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs546168468 Functional Loss SNV dbSNP153 33..33 33 - - - 13318 RMVar_ID_13318 Human_SNP_ID_15784064 A-to-I Human chr1 + 62159303 62159303 62159303 AACCTCCGCCTCCCAGGTTCAAGTGATTCTCCAGCCTCAGCCTCCCAAGTAGCTGGGATTACAGG AACCTCCGCCTCCCAGGTTCAAGTGATTCTCCGGCCTCAGCCTCCCAAGTAGCTGGGATTACAGG A G PATJ Ensembl:ENSG00000132849 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1282855269 Functional Loss SNV dbSNP153 33..33 33 - - - 13319 RMVar_ID_13319 Human_SNP_ID_15784632 A-to-I Human chr1 + 62161432 62161432 62161432 GCAATCTTGGCTCACTGCAACCTCGGCCTCCCAGGTTGGAGCGATTCTCCTGCCTCAGCCTCCCG GCAATCTTGGCTCACTGCAACCTCGGCCTCCCTGGTTGGAGCGATTCTCCTGCCTCAGCCTCCCG A T PATJ Ensembl:ENSG00000132849 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1447213956 Functional Loss SNV dbSNP153 33..33 33 - - - 13320 RMVar_ID_13320 Human_SNP_ID_15784637 A-to-I Human chr1 + 62161456 62161456 62161456 GGCCTCCCAGGTTGGAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCATGCA GGCCTCCCAGGTTGGAGCGATTCTCCTGCCTCCGCCTCCCGAGTAGCTGGGATTACAGGCATGCA A C PATJ Ensembl:ENSG00000132849 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs907236636 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1393703 13321 RMVar_ID_13321 Human_SNP_ID_15784648 A-to-I Human chr1 + 62161494 62161494 62161494 CCGAGTAGCTGGGATTACAGGCATGCATCACCACACTGGGTTTATTTTTGTTTTTTTAGTAGAGA CCGAGTAGCTGGGATTACAGGCATGCATCACCGCACTGGGTTTATTTTTGTTTTTTTAGTAGAGA A G PATJ Ensembl:ENSG00000132849 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048247616 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5849275 Human_miRNA_ID_503531,Human_miRNA_ID_510749 13322 RMVar_ID_13322 Human_SNP_ID_15784658 A-to-I Human chr1 + 62161539 62161539 62161539 TTTTGTTTTTTTAGTAGAGATGGAGCTTCCCCATGTGGGCCAGGCTGGTCTTGAACTTCTGACCT TTTTGTTTTTTTAGTAGAGATGGAGCTTCCCCGTGTGGGCCAGGCTGGTCTTGAACTTCTGACCT A G PATJ Ensembl:ENSG00000132849 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1273364796 Functional Loss SNV dbSNP153 33..33 33 - - - 13323 RMVar_ID_13323 Human_SNP_ID_15784956 A-to-I Human chr1 + 62162929 62162928 62162930 AGTTCGTGCCACTCCACTCCAGCCTGGGTGACAGAGCAAGACTCTGTCTCGAAAAAGAAAAAAAA AGTTCGTGCCACTCCACTCCAGCCTGGGTGAC__AGCAAGACTCTGTCTCGAAAAAGAAAAAAAA CAG C PATJ Ensembl:ENSG00000132849 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1450434262 Functional Loss DEL dbSNP153 33..34 33 - - - Human_Splice_Rec_79130 13324 RMVar_ID_13324 Human_SNP_ID_15784957 A-to-I Human chr1 + 62162929 62162929 62162929 AGTTCGTGCCACTCCACTCCAGCCTGGGTGACAGAGCAAGACTCTGTCTCGAAAAAGAAAAAAAA AGTTCGTGCCACTCCACTCCAGCCTGGGTGACGGAGCAAGACTCTGTCTCGAAAAAGAAAAAAAA A G PATJ Ensembl:ENSG00000132849 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1409859372 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_79130 13325 RMVar_ID_13325 Human_SNP_ID_15784960 A-to-I Human chr1 + 62162934 62162934 62162934 GTGCCACTCCACTCCAGCCTGGGTGACAGAGCAAGACTCTGTCTCGAAAAAGAAAAAAAACCATG GTGCCACTCCACTCCAGCCTGGGTGACAGAGCGAGACTCTGTCTCGAAAAAGAAAAAAAACCATG A G PATJ Ensembl:ENSG00000132849 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1222531600 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_79130 13326 RMVar_ID_13326 Human_SNP_ID_15856834 A-to-I Human chr1 - 62442836 62442836 62442836 ATGACGCCCTACTAGTTTTTGTATTTTTAGTAAAGACAGGGTCTTGCCATGTTACCCAGGCTGGT ATGACGCCCTACTAGTTTTTGTATTTTTAGTAGAGACAGGGTCTTGCCATGTTACCCAGGCTGGT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1433613043 Functional Loss SNV dbSNP153 33..33 33 - - - 13327 RMVar_ID_13327 Human_SNP_ID_15857170 A-to-I Human chr1 + 62444099 62444099 62444099 TGGCCAACATGGTGAAACCCTGCCCCTACTAAAAATACAAAAATTAGCTGGGTGTGGTGGTTTGC TGGCCAACATGGTGAAACCCTGCCCCTACTAACAATACAAAAATTAGCTGGGTGTGGTGGTTTGC A C USP1 Ensembl:ENSG00000162607 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904226940 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51448,RMVar_hsa_circ_133487,RMVar_hsa_circ_107857,RMVar_hsa_circ_318303,RMVar_hsa_circ_133490,RMVar_hsa_circ_133495,RMVar_hsa_circ_294607,RMVar_hsa_circ_326952,RMVar_hsa_circ_133491,RMVar_hsa_circ_377251,RMVar_hsa_circ_133497,RMVar_hsa_circ_133499,RMVar_hsa_circ_299764,RMVar_hsa_circ_328741,RMVar_hsa_circ_272674,RMVar_hsa_circ_133498,RMVar_hsa_circ_133496 13328 RMVar_ID_13328 Human_SNP_ID_15858733 A-to-I Human chr1 + 62449093 62449093 62449093 TTTAGTAGAGACAGGATTTCACCATGTTGCCCAGTCTGATCTTGAACTTCTGGACTCAAGCAATC TTTAGTAGAGACAGGATTTCACCATGTTGCCCCGTCTGATCTTGAACTTCTGGACTCAAGCAATC A C USP1 Ensembl:ENSG00000162607 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs530843098 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11063038 RMVar_hsa_circ_133499 13329 RMVar_ID_13329 Human_SNP_ID_15858734 A-to-I Human chr1 + 62449105 62449094 62449105 AGGATTTCACCATGTTGCCCAGTCTGATCTTGAACTTCTGGACTCAAGCAATCCACCTGCCTTAG AGGATTTCACCATGTTGCCCAG___________ACTTCTGGACTCAAGCAATCCACCTGCCTTAG GTCTGATCTTGA G USP1 Ensembl:ENSG00000162607 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1227964514 Functional Loss DEL dbSNP153 23..33 33 - - - Human_RBP_ID_11063040 RMVar_hsa_circ_133499 13330 RMVar_ID_13330 Human_SNP_ID_15858859 A-to-I Human chr1 + 62449654 62449654 62449654 TGACTAAAATGGGCTGGGCGTGGGTGGCTCACACCTGTAATCCTAGCACTTTGGGAGGCTGAGAT TGACTAAAATGGGCTGGGCGTGGGTGGCTCACGCCTGTAATCCTAGCACTTTGGGAGGCTGAGAT A G USP1 Ensembl:ENSG00000162607 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1367922764 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_133499 13331 RMVar_ID_13331 Human_SNP_ID_15858875 A-to-I Human chr1 + 62449725 62449725 62449725 CTTGCACCCAGGAGTTCAAGACCAGCCTGGGCAACATGACAAAACCCTATCTCTACAAAAAATAC CTTGCACCCAGGAGTTCAAGACCAGCCTGGGCGACATGACAAAACCCTATCTCTACAAAAAATAC A G USP1 Ensembl:ENSG00000162607 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs778601374 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_133499 13332 RMVar_ID_13332 Human_SNP_ID_15858879 A-to-I Human chr1 + 62449741 62449741 62449741 CAAGACCAGCCTGGGCAACATGACAAAACCCTATCTCTACAAAAAATACACAAACTAGTTTGGCG CAAGACCAGCCTGGGCAACATGACAAAACCCTCTCTCTACAAAAAATACACAAACTAGTTTGGCG A C USP1 Ensembl:ENSG00000162607 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs941839974 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11063063 RMVar_hsa_circ_133499 13333 RMVar_ID_13333 Human_SNP_ID_15859687 A-to-I Human chr1 + 62452417 62452416 62452417 GGGCGTGGTGGCAGGCATCTGTAGTCCCAGCTACTCAGGAGGCGGAGGCAGGAGAATGGCATGAA GGGCGTGGTGGCAGGCATCTGTAGTCCCAGCT_CTCAGGAGGCGGAGGCAGGAGAATGGCATGAA TA T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1557560855 Functional Loss DEL dbSNP153 33..33 33 - - - 13334 RMVar_ID_13334 Human_SNP_ID_15867759 A-to-I Human chr1 - 62485098 62485098 62485098 GGGGTCTCACTCTGTAATTCAGACTGGAGTGCAGTGGCACGATCACAGCTCACTGCAGCCTTGAC GGGGTCTCACTCTGTAATTCAGACTGGAGTGCTGTGGCACGATCACAGCTCACTGCAGCCTTGAC T A DOCK7 Ensembl:ENSG00000116641 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs931362184 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7408,RMVar_hsa_circ_325691,RMVar_hsa_circ_349508,RMVar_hsa_circ_346071,RMVar_hsa_circ_306259,RMVar_hsa_circ_49268,RMVar_hsa_circ_20283,RMVar_hsa_circ_25039,RMVar_hsa_circ_133505,RMVar_hsa_circ_133507,RMVar_hsa_circ_133508,RMVar_hsa_circ_133506,RMVar_hsa_circ_133504 13335 RMVar_ID_13335 Human_SNP_ID_15867760 A-to-I Human chr1 - 62485098 62485098 62485098 GGGGTCTCACTCTGTAATTCAGACTGGAGTGCAGTGGCACGATCACAGCTCACTGCAGCCTTGAC GGGGTCTCACTCTGTAATTCAGACTGGAGTGCGGTGGCACGATCACAGCTCACTGCAGCCTTGAC T C DOCK7 Ensembl:ENSG00000116641 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs931362184 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7408,RMVar_hsa_circ_325691,RMVar_hsa_circ_349508,RMVar_hsa_circ_346071,RMVar_hsa_circ_306259,RMVar_hsa_circ_49268,RMVar_hsa_circ_20283,RMVar_hsa_circ_25039,RMVar_hsa_circ_133505,RMVar_hsa_circ_133507,RMVar_hsa_circ_133508,RMVar_hsa_circ_133506,RMVar_hsa_circ_133504 13336 RMVar_ID_13336 Human_SNP_ID_15879186 A-to-I Human chr1 - 62534493 62534493 62534493 CTTCTGCCTCAGCCTTCTGAGTAGTTGGGACTACAGGCGCGTGCCACCACTCCCGGCTAATTTTT CTTCTGCCTCAGCCTTCTGAGTAGTTGGGACTGCAGGCGCGTGCCACCACTCCCGGCTAATTTTT T C DOCK7 Ensembl:ENSG00000116641 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs754662753 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11082,RMVar_hsa_circ_18828,RMVar_hsa_circ_7408,RMVar_hsa_circ_49268,RMVar_hsa_circ_133504,RMVar_hsa_circ_19927,RMVar_hsa_circ_30894,RMVar_hsa_circ_100441,RMVar_hsa_circ_267612,RMVar_hsa_circ_133517,RMVar_hsa_circ_25335,RMVar_hsa_circ_133515,RMVar_hsa_circ_120908,RMVar_hsa_circ_371628,RMVar_hsa_circ_133518,RMVar_hsa_circ_299795,RMVar_hsa_circ_24655,RMVar_hsa_circ_287700,RMVar_hsa_circ_342802,RMVar_hsa_circ_83708,RMVar_hsa_circ_33622,RMVar_hsa_circ_133520,RMVar_hsa_circ_133521,RMVar_hsa_circ_127726,RMVar_hsa_circ_287160,RMVar_hsa_circ_328919,RMVar_hsa_circ_133526,RMVar_hsa_circ_376427,RMVar_hsa_circ_290283,RMVar_hsa_circ_49110,RMVar_hsa_circ_22996,RMVar_hsa_circ_320111,RMVar_hsa_circ_133527,RMVar_hsa_circ_327097,RMVar_hsa_circ_337047,RMVar_hsa_circ_364798,RMVar_hsa_circ_40303,RMVar_hsa_circ_90132,RMVar_hsa_circ_32086,RMVar_hsa_circ_49088,RMVar_hsa_circ_133529,RMVar_hsa_circ_133531,RMVar_hsa_circ_133532,RMVar_hsa_circ_133530,RMVar_hsa_circ_133528 13337 RMVar_ID_13337 Human_SNP_ID_15900740 A-to-I Human chr1 - 62622592 62622592 62622592 AATATTAGCCGGCCATGTTGGTGTATACCTGTAGTCCCAGCTACTTGGGAGGCTGAGACGGGAGA AATATTAGCCGGCCATGTTGGTGTATACCTGTGGTCCCAGCTACTTGGGAGGCTGAGACGGGAGA T C DOCK7 Ensembl:ENSG00000116641 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs983442864 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2531,RMVar_hsa_circ_11082,RMVar_hsa_circ_83708,RMVar_hsa_circ_133520,RMVar_hsa_circ_90132,RMVar_hsa_circ_133532,RMVar_hsa_circ_304865,RMVar_hsa_circ_9578,RMVar_hsa_circ_50230,RMVar_hsa_circ_55426,RMVar_hsa_circ_12109,RMVar_hsa_circ_133555,RMVar_hsa_circ_344356,RMVar_hsa_circ_376219,RMVar_hsa_circ_52046,RMVar_hsa_circ_375977,RMVar_hsa_circ_297637,RMVar_hsa_circ_11815,RMVar_hsa_circ_133556,RMVar_hsa_circ_133557,RMVar_hsa_circ_63598,RMVar_hsa_circ_133554,RMVar_hsa_circ_133559,RMVar_hsa_circ_346383,RMVar_hsa_circ_314590,RMVar_hsa_circ_368900,RMVar_hsa_circ_133561,RMVar_hsa_circ_7480,RMVar_hsa_circ_133560,RMVar_hsa_circ_331237,RMVar_hsa_circ_341231,RMVar_hsa_circ_316648,RMVar_hsa_circ_300417,RMVar_hsa_circ_133563,RMVar_hsa_circ_133564,RMVar_hsa_circ_133565,RMVar_hsa_circ_133566,RMVar_hsa_circ_378978 13338 RMVar_ID_13338 Human_SNP_ID_15900741 A-to-I Human chr1 - 62622592 62622592 62622592 AATATTAGCCGGCCATGTTGGTGTATACCTGTAGTCCCAGCTACTTGGGAGGCTGAGACGGGAGA AATATTAGCCGGCCATGTTGGTGTATACCTGTCGTCCCAGCTACTTGGGAGGCTGAGACGGGAGA T G DOCK7 Ensembl:ENSG00000116641 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs983442864 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2531,RMVar_hsa_circ_11082,RMVar_hsa_circ_83708,RMVar_hsa_circ_133520,RMVar_hsa_circ_90132,RMVar_hsa_circ_133532,RMVar_hsa_circ_304865,RMVar_hsa_circ_9578,RMVar_hsa_circ_50230,RMVar_hsa_circ_55426,RMVar_hsa_circ_12109,RMVar_hsa_circ_133555,RMVar_hsa_circ_344356,RMVar_hsa_circ_376219,RMVar_hsa_circ_52046,RMVar_hsa_circ_375977,RMVar_hsa_circ_297637,RMVar_hsa_circ_11815,RMVar_hsa_circ_133556,RMVar_hsa_circ_133557,RMVar_hsa_circ_63598,RMVar_hsa_circ_133554,RMVar_hsa_circ_133559,RMVar_hsa_circ_346383,RMVar_hsa_circ_314590,RMVar_hsa_circ_368900,RMVar_hsa_circ_133561,RMVar_hsa_circ_7480,RMVar_hsa_circ_133560,RMVar_hsa_circ_331237,RMVar_hsa_circ_341231,RMVar_hsa_circ_316648,RMVar_hsa_circ_300417,RMVar_hsa_circ_133563,RMVar_hsa_circ_133564,RMVar_hsa_circ_133565,RMVar_hsa_circ_133566,RMVar_hsa_circ_378978 13339 RMVar_ID_13339 Human_SNP_ID_16091857 A-to-I Human chr1 + 63421278 63421278 63421278 TTGGCTCACCACAACCTCCGCCTCCCTAGTTCAAGCGATTCTCCTGCCTCAGTGATCATTAAAAA TTGGCTCACCACAACCTCCGCCTCCCTAGTTCTAGCGATTCTCCTGCCTCAGTGATCATTAAAAA A T ALG6 Ensembl:ENSG00000088035 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs919462149 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34288,RMVar_hsa_circ_323317,RMVar_hsa_circ_304283,RMVar_hsa_circ_133590,RMVar_hsa_circ_133591 13340 RMVar_ID_13340 Human_SNP_ID_16092811 A-to-I Human chr1 + 63422943 63422943 63422943 CACCATTGCATTCCAGCATGGGCAACGAGAGCAAAACTCCGTCTCAAAAAACAAAGGAAACAAAA CACCATTGCATTCCAGCATGGGCAACGAGAGCCAAACTCCGTCTCAAAAAACAAAGGAAACAAAA A C ALG6 Ensembl:ENSG00000088035 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1227698613 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34288,RMVar_hsa_circ_323317,RMVar_hsa_circ_304283,RMVar_hsa_circ_133590,RMVar_hsa_circ_133591 13341 RMVar_ID_13341 Human_SNP_ID_16092889 A-to-I Human chr1 + 63423198 63423198 63423198 GACGCACACCACCACGCCCAGCTAATTTTTGTATTTTTGGAAGAGAAAGGGTTTCACCATGTTGG GACGCACACCACCACGCCCAGCTAATTTTTGTCTTTTTGGAAGAGAAAGGGTTTCACCATGTTGG A C ALG6 Ensembl:ENSG00000088035 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1252018051 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34288,RMVar_hsa_circ_323317,RMVar_hsa_circ_304283,RMVar_hsa_circ_133590,RMVar_hsa_circ_133591 13342 RMVar_ID_13342 Human_SNP_ID_16098062 A-to-I Human chr1 - 63445885 63445885 63445885 AAAAACAACAACAAAAACTGGCATTAGGGGCTAGGCATGGTGATTCATGCCTGTAATCCCAGCAC AAAAACAACAACAAAAACTGGCATTAGGGGCTGGGCATGGTGATTCATGCCTGTAATCCCAGCAC T C ITGB3BP Ensembl:ENSG00000142856 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1019310297 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112159,RMVar_hsa_circ_133592 13343 RMVar_ID_13343 Human_SNP_ID_16098096 A-to-I Human chr1 - 63446028 63446028 63446028 CCGGCTAGCTTGCGCCTGAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACCCA CCGGCTAGCTTGCGCCTGAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCA T C ITGB3BP Ensembl:ENSG00000142856 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031643914 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112159,RMVar_hsa_circ_133592 13344 RMVar_ID_13344 Human_SNP_ID_16099582 A-to-I Human chr1 - 63452636 63452633 63452636 GGATGTGGCTTGGGATCTTTTAAAAAAAAAAAAAAGAAAGAAAAGAAAAAGAAAAAAGAAAAATT GGATGTGGCTTGGGATCTTTTAAAAAAAAAAA___GAAAGAAAAGAAAAAGAAAAAAGAAAAATT CTTT C ITGB3BP Ensembl:ENSG00000142856 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs57856763 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_112159,RMVar_hsa_circ_265191,RMVar_hsa_circ_133592,RMVar_hsa_circ_296826 13345 RMVar_ID_13345 Human_SNP_ID_16099583 A-to-I Human chr1 - 63452636 63452633 63452636 GGATGTGGCTTGGGATCTTTTAAAAAAAAAAAAAAGAAAGAAAAGAAAAAGAAAAAAGAAAAATT GGATGTGGCTTGGGATCTTTTAAAAAAAAAAA_AAGAAAGAAAAGAAAAAGAAAAAAGAAAAATT CTTT CTT ITGB3BP Ensembl:ENSG00000142856 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs57856763 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_112159,RMVar_hsa_circ_265191,RMVar_hsa_circ_133592,RMVar_hsa_circ_296826 13346 RMVar_ID_13346 Human_SNP_ID_16102659 A-to-I Human chr1 - 63467110 63467110 63467110 AGGAGGCCAAGGAGGGAGGATCACTTGAGGCAAGGAGTTAGAGACCAGCCTGGGCAACAAAATGA AGGAGGCCAAGGAGGGAGGATCACTTGAGGCATGGAGTTAGAGACCAGCCTGGGCAACAAAATGA T A ITGB3BP Ensembl:ENSG00000142856 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs919053153 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2160212,Human_RBP_ID_11066773 RMVar_hsa_circ_62813,RMVar_hsa_circ_112159,RMVar_hsa_circ_133592,RMVar_hsa_circ_353628,RMVar_hsa_circ_133593 13347 RMVar_ID_13347 Human_SNP_ID_16107012 A-to-I Human chr1 - 63482818 63482818 63482818 AAAACCCAGTCTCTACTAAAAATACAAAAATTAGCCAGGCGTGGTGGTGCACGCTTGCAGTCCCA AAAACCCAGTCTCTACTAAAAATACAAAAATTCGCCAGGCGTGGTGGTGCACGCTTGCAGTCCCA T G ITGB3BP Ensembl:ENSG00000142856 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909576973 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112159,RMVar_hsa_circ_133592,RMVar_hsa_circ_353628,RMVar_hsa_circ_133594,RMVar_hsa_circ_285222,RMVar_hsa_circ_133593,RMVar_hsa_circ_293744,RMVar_hsa_circ_133595 13348 RMVar_ID_13348 Human_SNP_ID_16107248 A-to-I Human chr1 - 63483933 63483933 63483933 GATTTTGTCATTGTATGAACATCATAGATTGTACTTACACAAACCTAGATGTCATAGCCTACTAC GATTTTGTCATTGTATGAACATCATAGATTGTGCTTACACAAACCTAGATGTCATAGCCTACTAC T C ITGB3BP Ensembl:ENSG00000142856 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs770836771 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112159,RMVar_hsa_circ_133592,RMVar_hsa_circ_353628,RMVar_hsa_circ_133594,RMVar_hsa_circ_285222,RMVar_hsa_circ_133593,RMVar_hsa_circ_293744,RMVar_hsa_circ_133595 13349 RMVar_ID_13349 Human_SNP_ID_16109672 A-to-I Human chr1 - 63494318 63494313 63494319 GGTCAGGAGTTGGAGACCAACCTGGTGAACATAGTGAAACCTTGTCTCTACTAAAAATACACAAA GGTCAGGAGTTGGAGACCAACCTGGTGAACA______AACCTTGTCTCTACTAAAAATACACAAA TTCACTA T ITGB3BP Ensembl:ENSG00000142856 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1188905027 Functional Loss DEL dbSNP153 32..37 33 - - - RMVar_hsa_circ_285222,RMVar_hsa_circ_133595 13350 RMVar_ID_13350 Human_SNP_ID_16109674 A-to-I Human chr1 - 63494318 63494318 63494318 GGTCAGGAGTTGGAGACCAACCTGGTGAACATAGTGAAACCTTGTCTCTACTAAAAATACACAAA GGTCAGGAGTTGGAGACCAACCTGGTGAACATCGTGAAACCTTGTCTCTACTAAAAATACACAAA T G ITGB3BP Ensembl:ENSG00000142856 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1464263834 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_285222,RMVar_hsa_circ_133595 13351 RMVar_ID_13351 Human_SNP_ID_16131151 A-to-I Human chr1 - 63589166 63589166 63589166 CCCATCTCTACTAAAAATACAAAAAATTAGCCAGGTGTCGTGGCAGGTGCCTGTAGTCCCAGCTA CCCATCTCTACTAAAAATACAAAAAATTAGCCGGGTGTCGTGGCAGGTGCCTGTAGTCCCAGCTA T C ITGB3BP Ensembl:ENSG00000142856 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1416367225 Functional Loss SNV dbSNP153 33..33 33 - - - 13352 RMVar_ID_13352 Human_SNP_ID_16131167 A-to-I Human chr1 - 63589208 63589206 63589208 GAGGTCAGGAGATCGAGATCATCCTGGCTAACAGGGTAAAAACCCATCTCTACTAAAAATACAAA GAGGTCAGGAGATCGAGATCATCCTGGCTAAC__GGTAAAAACCCATCTCTACTAAAAATACAAA CCT C ITGB3BP Ensembl:ENSG00000142856 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1234884377 Functional Loss DEL dbSNP153 33..34 33 - - - 13353 RMVar_ID_13353 Human_SNP_ID_16131273 A-to-I Human chr1 - 63589623 63589623 63589623 GGGTTCAAGCAATGCTCGTGTCTCAGCCTCCCAAGTAGTTGGAATTACAGGCACATGCCACTATG GGGTTCAAGCAATGCTCGTGTCTCAGCCTCCCGAGTAGTTGGAATTACAGGCACATGCCACTATG T C ITGB3BP Ensembl:ENSG00000142856 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1339541720 Functional Loss SNV dbSNP153 33..33 33 - - - 13354 RMVar_ID_13354 Human_SNP_ID_16131453 A-to-I Human chr1 - 63590331 63590331 63590331 GAATGTAACGAAGGTCAAAATACTTCTTCCTCAATGTTTATAAGCTGTACTGTAACTGCTGTGAG GAATGTAACGAAGGTCAAAATACTTCTTCCTCGATGTTTATAAGCTGTACTGTAACTGCTGTGAG T C ITGB3BP Ensembl:ENSG00000142856 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs749985471 Functional Loss SNV dbSNP153 33..33 33 - - - 13355 RMVar_ID_13355 Human_SNP_ID_16131454 A-to-I Human chr1 - 63590331 63590331 63590331 GAATGTAACGAAGGTCAAAATACTTCTTCCTCAATGTTTATAAGCTGTACTGTAACTGCTGTGAG GAATGTAACGAAGGTCAAAATACTTCTTCCTCCATGTTTATAAGCTGTACTGTAACTGCTGTGAG T G ITGB3BP Ensembl:ENSG00000142856 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs749985471 Functional Loss SNV dbSNP153 33..33 33 - - - 13356 RMVar_ID_13356 Human_SNP_ID_16131531 A-to-I Human chr1 - 63590796 63590796 63590796 CAGCTTATAAACATCAAGGAGAAAGTATTTTGACCTTCATTAAATTCTTTTTAAGGCAAGCATAC CAGCTTATAAACATCAAGGAGAAAGTATTTTGGCCTTCATTAAATTCTTTTTAAGGCAAGCATAC T C ITGB3BP Ensembl:ENSG00000142856 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs988058516 Functional Loss SNV dbSNP153 33..33 33 - - - 13357 RMVar_ID_13357 Human_SNP_ID_16133588 A-to-I Human chr1 + 63598028 63598028 63598028 GTCTTACTCTGTTGCCCAGACTGCAGCACAGTAGCGCGATCGTGGCTTACTGCAGCCTCAGTCTC GTCTTACTCTGTTGCCCAGACTGCAGCACAGTGGCGCGATCGTGGCTTACTGCAGCCTCAGTCTC A G PGM1 Ensembl:ENSG00000079739 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1039103237 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85104,RMVar_hsa_circ_88997,RMVar_hsa_circ_133609,RMVar_hsa_circ_133610 13358 RMVar_ID_13358 Human_SNP_ID_16178446 A-to-I Human chr1 - 63788974 63788973 63788975 GGATTCTGTGCTGGCTGCTCAGAAGATACCGCATATCTAAGAAGATTGATCACCTCATGTATCAC GGATTCTGTGCTGGCTGCTCAGAAGATACCG__TATCTAAGAAGATTGATCACCTCATGTATCAC ATG A AL161742.1 Ensembl:ENSG00000177452 Pseudogene exon GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1455305418 Functional Loss DEL dbSNP153 32..33 33 - - - 13359 RMVar_ID_13359 Human_SNP_ID_16178447 A-to-I Human chr1 - 63788974 63788974 63788974 GGATTCTGTGCTGGCTGCTCAGAAGATACCGCATATCTAAGAAGATTGATCACCTCATGTATCAC GGATTCTGTGCTGGCTGCTCAGAAGATACCGCGTATCTAAGAAGATTGATCACCTCATGTATCAC T C AL161742.1 Ensembl:ENSG00000177452 Pseudogene exon GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs992255114 Functional Loss SNV dbSNP153 33..33 33 - - - 13360 RMVar_ID_13360 Human_SNP_ID_16178504 A-to-I Human chr1 - 63789126 63789126 63789126 GATGATCCGCAAGCCAATGACTGTCCATTCCCAGGCTCGATGCCAGGAAAACACCTTGGCCTACC GATGATCCGCAAGCCAATGACTGTCCATTCCCCGGCTCGATGCCAGGAAAACACCTTGGCCTACC T G AL161742.1 Ensembl:ENSG00000177452 Pseudogene exon GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1389867012 Functional Loss SNV dbSNP153 33..33 33 - - - 13361 RMVar_ID_13361 Human_SNP_ID_16180720 A-to-I Human chr1 + 63799129 63799129 63799129 ATCTGTAAAGAAGAGATGATCATGTCTACCTTAAAAGGCTGCTAGGAAAACTAGAGATAATACAT ATCTGTAAAGAAGAGATGATCATGTCTACCTTGAAAGGCTGCTAGGAAAACTAGAGATAATACAT A G ROR1 Ensembl:ENSG00000185483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170078706 Functional Loss SNV dbSNP153 33..33 33 - - - 13362 RMVar_ID_13362 Human_SNP_ID_16190381 A-to-I Human chr1 - 63843287 63843287 63843287 GTCAAGAAGCTGACAGGGATCAAGCATGAATTACACACAAACTGCTACAAGGAGGTCAAGGACCG GTCAAGAAGCTGACAGGGATCAAGCATGAATTGCACACAAACTGCTACAAGGAGGTCAAGGACCG T C CFL1P3 Ensembl:ENSG00000228056 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878981480 Functional Loss SNV dbSNP153 33..33 33 - - - 13363 RMVar_ID_13363 Human_SNP_ID_16356645 A-to-I Human chr1 + 64561813 64561813 64561813 CAAGGAGGTTGAGGCTACAGTGAACTGTGATGATGCCGCTGCACTCCAGTCTGGGGAACAGAGCA CAAGGAGGTTGAGGCTACAGTGAACTGTGATGTTGCCGCTGCACTCCAGTCTGGGGAACAGAGCA A T CACHD1 Ensembl:ENSG00000158966 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs964969011 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7664,RMVar_hsa_circ_298110,RMVar_hsa_circ_323626,RMVar_hsa_circ_327998,RMVar_hsa_circ_311343,RMVar_hsa_circ_285543,RMVar_hsa_circ_133625,RMVar_hsa_circ_133623,RMVar_hsa_circ_133624,RMVar_hsa_circ_133622 13364 RMVar_ID_13364 Human_SNP_ID_16439273 A-to-I Human chr1 - 64916774 64916774 64916774 GGAGTTCAGCGGCAGAATCTCGGCTCACTGCAACCTCTGCCTCCCGGTTCAAGCGATTCTCCCAC GGAGTTCAGCGGCAGAATCTCGGCTCACTGCAGCCTCTGCCTCCCGGTTCAAGCGATTCTCCCAC T C JAK1 Ensembl:ENSG00000162434 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1158930231 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123711,RMVar_hsa_circ_133664 13365 RMVar_ID_13365 Human_SNP_ID_16453607 A-to-I Human chr1 - 64977523 64977523 64977523 GGGAGGCTGAGGCAGGAGAATGGCAGGAACCCAGGAGGCAGAGCTTGCAGTGAGCCAAGATTGCT GGGAGGCTGAGGCAGGAGAATGGCAGGAACCCGGGAGGCAGAGCTTGCAGTGAGCCAAGATTGCT T C JAK1,LINC01359 Ensembl:ENSG00000162434,Ensembl:ENSG00000226891 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1374583332 Functional Loss SNV dbSNP153 33..33 33 - - - 13366 RMVar_ID_13366 Human_SNP_ID_16455251 A-to-I Human chr1 + 64984823 64984823 64984823 GAAGATAATAAAAACGTAGGCTCCTAAATAGTAAGCAGCAGAAGGGAAAAGCAATCTGACTAGGA GAAGATAATAAAAACGTAGGCTCCTAAATAGTGAGCAGCAGAAGGGAAAAGCAATCTGACTAGGA A G lnc-AK4-1 RNACentral:URS0000D5D7C7 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1056184117 Functional Loss SNV dbSNP153 33..33 33 - - - 13367 RMVar_ID_13367 Human_SNP_ID_16469639 A-to-I Human chr1 - 65047157 65047157 65047157 AAATTTTTTGGAGACAGGGTTTTACCCAGGCTAGAGTTCAATGGCATAATCGTAGGTCACTGTTG AAATTTTTTGGAGACAGGGTTTTACCCAGGCTGGAGTTCAATGGCATAATCGTAGGTCACTGTTG T C JAK1 Ensembl:ENSG00000162434 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971439465 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11074416 13368 RMVar_ID_13368 Human_SNP_ID_16470895 A-to-I Human chr1 - 65052119 65052119 65052119 CTGTCTCTACCAAAAAAAAAAAAAAAAAAAAAATAGCCAGGCGTGGTGGTGCATGCTTGTAGTCC CTGTCTCTACCAAAAAAAAAAAAAAAAAAAAAGTAGCCAGGCGTGGTGGTGCATGCTTGTAGTCC T C JAK1 Ensembl:ENSG00000162434 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1383600771 Functional Loss SNV dbSNP153 33..33 33 - - - 13369 RMVar_ID_13369 Human_SNP_ID_16471096 A-to-I Human chr1 - 65052692 65052692 65052692 CTCCTGCCTCAGCCTCCCAAGTAGCTGGAACTACAGGCACCCACCACCACACCCGGCTAAGTTTT CTCCTGCCTCAGCCTCCCAAGTAGCTGGAACTGCAGGCACCCACCACCACACCCGGCTAAGTTTT T C JAK1 Ensembl:ENSG00000162434 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1263552270 Functional Loss SNV dbSNP153 33..33 33 - - - 13370 RMVar_ID_13370 Human_SNP_ID_16471185 A-to-I Human chr1 - 65052909 65052909 65052909 CTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCATGCGCCGCCATGCTTGGCTAATTTTT CTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTGCAGGCATGCGCCGCCATGCTTGGCTAATTTTT T C JAK1 Ensembl:ENSG00000162434 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1469164238 Functional Loss SNV dbSNP153 33..33 33 - - - 13371 RMVar_ID_13371 Human_SNP_ID_16471512 A-to-I Human chr1 - 65053731 65053729 65053731 TTGTAGCCTCAGCCTCCTGATTAGCTGAGACTATGGGTGTGCACCACCATGCCCGGCTAATTTTT TTGTAGCCTCAGCCTCCTGATTAGCTGAGACT__GGGTGTGCACCACCATGCCCGGCTAATTTTT CAT C JAK1 Ensembl:ENSG00000162434 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027041690 Functional Loss DEL dbSNP153 33..34 33 - - - 13372 RMVar_ID_13372 Human_SNP_ID_16471513 A-to-I Human chr1 - 65053731 65053731 65053731 TTGTAGCCTCAGCCTCCTGATTAGCTGAGACTATGGGTGTGCACCACCATGCCCGGCTAATTTTT TTGTAGCCTCAGCCTCCTGATTAGCTGAGACTGTGGGTGTGCACCACCATGCCCGGCTAATTTTT T C JAK1 Ensembl:ENSG00000162434 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1269457526 Functional Loss SNV dbSNP153 33..33 33 - - - 13373 RMVar_ID_13373 Human_SNP_ID_16497509 A-to-I Human chr1 + 65157528 65157528 65157528 CAATTGGGCTGGGTGTGGTGGTTCATGTTTGTAATCCCAGCACTTTGGGAGGCTGAGGCTGGAGG CAATTGGGCTGGGTGTGGTGGTTCATGTTTGTCATCCCAGCACTTTGGGAGGCTGAGGCTGGAGG A C AK4 Ensembl:ENSG00000162433 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1479036058 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_133684,RMVar_hsa_circ_120407,RMVar_hsa_circ_133685,RMVar_hsa_circ_97213 13374 RMVar_ID_13374 Human_SNP_ID_16514372 A-to-I Human chr1 - 65227635 65227635 65227635 AAGTTAGACAGGAGTCACTCCCAAGAATAGTAAAGGACACTCACTGGGGACAGTCATGATGGGTG AAGTTAGACAGGAGTCACTCCCAAGAATAGTAGAGGACACTCACTGGGGACAGTCATGATGGGTG T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs866240256 Functional Loss SNV dbSNP153 33..33 33 - - - 13375 RMVar_ID_13375 Human_SNP_ID_16524786 A-to-I Human chr1 + 65271818 65271818 65271818 CTTGAACTAGGAGGTGGAGATTGCAGTGAGCCAAGATCACACCACTGTACACTCCAGCCTGGGCA CTTGAACTAGGAGGTGGAGATTGCAGTGAGCCGAGATCACACCACTGTACACTCCAGCCTGGGCA A G DNAJC6 Ensembl:ENSG00000116675 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs926811518 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5233994 13376 RMVar_ID_13376 Human_SNP_ID_16582234 A-to-I Human chr1 + 65521979 65521979 65521979 AAAATTACGTGGGTGTAGTGGTGGACACCTGTAATCCCAGCTACTCGGAAGGCTTTTATATGCAT AAAATTACGTGGGTGTAGTGGTGGACACCTGTTATCCCAGCTACTCGGAAGGCTTTTATATGCAT A T LEPR Ensembl:ENSG00000116678 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs932441135 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_367796,RMVar_hsa_circ_106328,RMVar_hsa_circ_133704 13377 RMVar_ID_13377 Human_SNP_ID_16595981 A-to-I Human chr1 + 65576518 65576518 65576518 ATAGAGCCTTCCAAGTTGAAGGACTTTGGGGCATTTTGGCCCTCTACTGATAAAAGTGGGTTGCT ATAGAGCCTTCCAAGTTGAAGGACTTTGGGGCGTTTTGGCCCTCTACTGATAAAAGTGGGTTGCT A G LEPR Ensembl:ENSG00000116678 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1248631598 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557922 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 13378 RMVar_ID_13378 Human_SNP_ID_16695907 A-to-I Human chr1 + 66010865 66010865 66010865 GGAGAGAAAGATGATTAATCTTCGTGGGGATGATGAGGCTGAGTATGGCATCACATGATGTCAAA GGAGAGAAAGATGATTAATCTTCGTGGGGATGGTGAGGCTGAGTATGGCATCACATGATGTCAAA A G PDE4B Ensembl:ENSG00000184588 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs961475298 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28245 13379 RMVar_ID_13379 Human_SNP_ID_16695921 A-to-I Human chr1 + 66010923 66010922 66010923 TGTCAAAAAGTCTCACAGGAAGAAAATGGAAGAAAGTCAAGGAAGTGGGAATTTTGAAAGTCATT TGTCAAAAAGTCTCACAGGAAGAAAATGGAAG_AAGTCAAGGAAGTGGGAATTTTGAAAGTCATT GA G PDE4B Ensembl:ENSG00000184588 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1276855656 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_28245 13380 RMVar_ID_13380 Human_SNP_ID_16697940 A-to-I Human chr1 + 66019530 66019530 66019530 GGTGTGCATTGAAATGCCTGGCTCATTTTTGTATTTTTAGCAAAGACAGGGTTTCACCATGTTGG GGTGTGCATTGAAATGCCTGGCTCATTTTTGTGTTTTTAGCAAAGACAGGGTTTCACCATGTTGG A G PDE4B Ensembl:ENSG00000184588 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs536250093 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28245 13381 RMVar_ID_13381 Human_SNP_ID_16710796 A-to-I Human chr1 + 66074939 66074939 66074939 CAGCTTTTGGCTATCGTGAATAGTTGTGATGTAGAGCAGGTGAGCCCCCAAATTGGGTCTTAGCG CAGCTTTTGGCTATCGTGAATAGTTGTGATGTGGAGCAGGTGAGCCCCCAAATTGGGTCTTAGCG A G PDE4B Ensembl:ENSG00000184588 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1393926616 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28245 13382 RMVar_ID_13382 Human_SNP_ID_16710850 A-to-I Human chr1 + 66075217 66075217 66075217 GCTGTCTAACACCACCAGCTCACCTTTGAATTATTTCCTGGGCAAAGCCAAAAATTATCCCATGC GCTGTCTAACACCACCAGCTCACCTTTGAATTCTTTCCTGGGCAAAGCCAAAAATTATCCCATGC A C PDE4B Ensembl:ENSG00000184588 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1307865982 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28245 13383 RMVar_ID_13383 Human_SNP_ID_16846792 A-to-I Human chr1 + 66630833 66630801 66630833 CGGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA C________________________________AGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA CGGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA C SGIP1 Ensembl:ENSG00000118473 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1305322872 Functional Loss DEL dbSNP153 2..33 33 - - - RMVar_hsa_circ_4541,RMVar_hsa_circ_43552,RMVar_hsa_circ_332811,RMVar_hsa_circ_279455,RMVar_hsa_circ_24753,RMVar_hsa_circ_9614,RMVar_hsa_circ_13121,RMVar_hsa_circ_7584,RMVar_hsa_circ_326390,RMVar_hsa_circ_133727 13384 RMVar_ID_13384 Human_SNP_ID_16846797 A-to-I Human chr1 + 66630829 66630801 66630829 ACTCCGGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA ACTCC____________________________AGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA CGGAAAGAAAGAAAGAAAGAAAGAAAGAA C SGIP1 Ensembl:ENSG00000118473 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1477504674 Functional Loss DEL dbSNP153 6..33 33 - - - RMVar_hsa_circ_4541,RMVar_hsa_circ_43552,RMVar_hsa_circ_332811,RMVar_hsa_circ_279455,RMVar_hsa_circ_24753,RMVar_hsa_circ_9614,RMVar_hsa_circ_13121,RMVar_hsa_circ_7584,RMVar_hsa_circ_326390,RMVar_hsa_circ_133727 13385 RMVar_ID_13385 Human_SNP_ID_16846802 A-to-I Human chr1 + 66630829 66630802 66630830 ACTCCGGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA ACTCCG____________________________GAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA GGAAAGAAAGAAAGAAAGAAAGAAAGAAA G SGIP1 Ensembl:ENSG00000118473 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs71058465 Functional Loss DEL dbSNP153 7..34 33 - - - RMVar_hsa_circ_4541,RMVar_hsa_circ_43552,RMVar_hsa_circ_332811,RMVar_hsa_circ_279455,RMVar_hsa_circ_24753,RMVar_hsa_circ_9614,RMVar_hsa_circ_13121,RMVar_hsa_circ_7584,RMVar_hsa_circ_326390,RMVar_hsa_circ_133727 13386 RMVar_ID_13386 Human_SNP_ID_16846803 A-to-I Human chr1 + 66630829 66630802 66630830 ACTCCGGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA ACTCCGGAAA________________________GAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA GGAAAGAAAGAAAGAAAGAAAGAAAGAAA GGAAA SGIP1 Ensembl:ENSG00000118473 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs71058465 Functional Loss DEL dbSNP153 11..34 33 - - - RMVar_hsa_circ_4541,RMVar_hsa_circ_43552,RMVar_hsa_circ_332811,RMVar_hsa_circ_279455,RMVar_hsa_circ_24753,RMVar_hsa_circ_9614,RMVar_hsa_circ_13121,RMVar_hsa_circ_7584,RMVar_hsa_circ_326390,RMVar_hsa_circ_133727 13387 RMVar_ID_13387 Human_SNP_ID_16846804 A-to-I Human chr1 + 66630829 66630802 66630830 ACTCCGGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA ACTCCGGAAAGAAA____________________GAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA GGAAAGAAAGAAAGAAAGAAAGAAAGAAA GGAAAGAAA SGIP1 Ensembl:ENSG00000118473 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs71058465 Functional Loss DEL dbSNP153 15..34 33 - - - RMVar_hsa_circ_4541,RMVar_hsa_circ_43552,RMVar_hsa_circ_332811,RMVar_hsa_circ_279455,RMVar_hsa_circ_24753,RMVar_hsa_circ_9614,RMVar_hsa_circ_13121,RMVar_hsa_circ_7584,RMVar_hsa_circ_326390,RMVar_hsa_circ_133727 13388 RMVar_ID_13388 Human_SNP_ID_16846805 A-to-I Human chr1 + 66630829 66630802 66630830 ACTCCGGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA ACTCCGGAAAGAAAGAAA________________GAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA GGAAAGAAAGAAAGAAAGAAAGAAAGAAA GGAAAGAAAGAAA SGIP1 Ensembl:ENSG00000118473 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs71058465 Functional Loss DEL dbSNP153 19..34 33 - - - RMVar_hsa_circ_4541,RMVar_hsa_circ_43552,RMVar_hsa_circ_332811,RMVar_hsa_circ_279455,RMVar_hsa_circ_24753,RMVar_hsa_circ_9614,RMVar_hsa_circ_13121,RMVar_hsa_circ_7584,RMVar_hsa_circ_326390,RMVar_hsa_circ_133727 13389 RMVar_ID_13389 Human_SNP_ID_16846806 A-to-I Human chr1 + 66630829 66630802 66630830 ACTCCGGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA ACTCCGGAAAGAAAGAAAGAAA____________GAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA GGAAAGAAAGAAAGAAAGAAAGAAAGAAA GGAAAGAAAGAAAGAAA SGIP1 Ensembl:ENSG00000118473 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs71058465 Functional Loss DEL dbSNP153 23..34 33 - - - RMVar_hsa_circ_4541,RMVar_hsa_circ_43552,RMVar_hsa_circ_332811,RMVar_hsa_circ_279455,RMVar_hsa_circ_24753,RMVar_hsa_circ_9614,RMVar_hsa_circ_13121,RMVar_hsa_circ_7584,RMVar_hsa_circ_326390,RMVar_hsa_circ_133727 13390 RMVar_ID_13390 Human_SNP_ID_16846807 A-to-I Human chr1 + 66630829 66630802 66630830 ACTCCGGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA ACTCCGGAAAGAAAGAAAGAAAGAAA________GAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA GGAAAGAAAGAAAGAAAGAAAGAAAGAAA GGAAAGAAAGAAAGAAAGAAA SGIP1 Ensembl:ENSG00000118473 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs71058465 Functional Loss DEL dbSNP153 27..34 33 - - - RMVar_hsa_circ_4541,RMVar_hsa_circ_43552,RMVar_hsa_circ_332811,RMVar_hsa_circ_279455,RMVar_hsa_circ_24753,RMVar_hsa_circ_9614,RMVar_hsa_circ_13121,RMVar_hsa_circ_7584,RMVar_hsa_circ_326390,RMVar_hsa_circ_133727 13391 RMVar_ID_13391 Human_SNP_ID_16846808 A-to-I Human chr1 + 66630829 66630802 66630830 ACTCCGGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA ACTCCGGAAAGAAAGAAAGAAAGAAAGAAA____GAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA GGAAAGAAAGAAAGAAAGAAAGAAAGAAA GGAAAGAAAGAAAGAAAGAAAGAAA SGIP1 Ensembl:ENSG00000118473 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs71058465 Functional Loss DEL dbSNP153 31..34 33 - - - RMVar_hsa_circ_4541,RMVar_hsa_circ_43552,RMVar_hsa_circ_332811,RMVar_hsa_circ_279455,RMVar_hsa_circ_24753,RMVar_hsa_circ_9614,RMVar_hsa_circ_13121,RMVar_hsa_circ_7584,RMVar_hsa_circ_326390,RMVar_hsa_circ_133727 13392 RMVar_ID_13392 Human_SNP_ID_16846846 A-to-I Human chr1 + 66630829 66630827 66630829 ACTCCGGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA ACTCCGGAAAGAAAGAAAGAAAGAAAGAAAG__AGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA GAA G SGIP1 Ensembl:ENSG00000118473 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1558132723 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_4541,RMVar_hsa_circ_43552,RMVar_hsa_circ_332811,RMVar_hsa_circ_279455,RMVar_hsa_circ_24753,RMVar_hsa_circ_9614,RMVar_hsa_circ_13121,RMVar_hsa_circ_7584,RMVar_hsa_circ_326390,RMVar_hsa_circ_133727 13393 RMVar_ID_13393 Human_SNP_ID_16846849 A-to-I Human chr1 + 66630829 66630829 66630829 ACTCCGGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA ACTCCGGAAAGAAAGAAAGAAAGAAAGAAAGAGAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA A G SGIP1 Ensembl:ENSG00000118473 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs186958489 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4541,RMVar_hsa_circ_43552,RMVar_hsa_circ_332811,RMVar_hsa_circ_279455,RMVar_hsa_circ_24753,RMVar_hsa_circ_9614,RMVar_hsa_circ_13121,RMVar_hsa_circ_7584,RMVar_hsa_circ_326390,RMVar_hsa_circ_133727 13394 RMVar_ID_13394 Human_SNP_ID_16846855 A-to-I Human chr1 + 66630833 66630831 66630833 CGGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA CGGAAAGAAAGAAAGAAAGAAAGAAAGAAAG__AGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA GAA G SGIP1 Ensembl:ENSG00000118473 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1411549450 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_4541,RMVar_hsa_circ_43552,RMVar_hsa_circ_332811,RMVar_hsa_circ_279455,RMVar_hsa_circ_24753,RMVar_hsa_circ_9614,RMVar_hsa_circ_13121,RMVar_hsa_circ_7584,RMVar_hsa_circ_326390,RMVar_hsa_circ_133727 13395 RMVar_ID_13395 Human_SNP_ID_16846856 A-to-I Human chr1 + 66630833 66630831 66630833 CGGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA CGGAAAGAAAGAAAGAAAGAAAGAAAGAAAGA_AGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA GAA GA SGIP1 Ensembl:ENSG00000118473 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1411549450 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_4541,RMVar_hsa_circ_43552,RMVar_hsa_circ_332811,RMVar_hsa_circ_279455,RMVar_hsa_circ_24753,RMVar_hsa_circ_9614,RMVar_hsa_circ_13121,RMVar_hsa_circ_7584,RMVar_hsa_circ_326390,RMVar_hsa_circ_133727 13396 RMVar_ID_13396 Human_SNP_ID_16846858 A-to-I Human chr1 + 66630833 66630833 66630833 CGGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA CGGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAGAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA A G SGIP1 Ensembl:ENSG00000118473 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs866936735 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4541,RMVar_hsa_circ_43552,RMVar_hsa_circ_332811,RMVar_hsa_circ_279455,RMVar_hsa_circ_24753,RMVar_hsa_circ_9614,RMVar_hsa_circ_13121,RMVar_hsa_circ_7584,RMVar_hsa_circ_326390,RMVar_hsa_circ_133727 13397 RMVar_ID_13397 Human_SNP_ID_16846862 A-to-I Human chr1 + 66630837 66630835 66630837 AAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA AAGAAAGAAAGAAAGAAAGAAAGAAAGAAAG__AGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA GAA G SGIP1 Ensembl:ENSG00000118473 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1301267457 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_4541,RMVar_hsa_circ_43552,RMVar_hsa_circ_332811,RMVar_hsa_circ_279455,RMVar_hsa_circ_24753,RMVar_hsa_circ_9614,RMVar_hsa_circ_13121,RMVar_hsa_circ_7584,RMVar_hsa_circ_326390,RMVar_hsa_circ_133727 13398 RMVar_ID_13398 Human_SNP_ID_16846865 A-to-I Human chr1 + 66630837 66630837 66630837 AAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA AAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAGAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA A G SGIP1 Ensembl:ENSG00000118473 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs190325446 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4541,RMVar_hsa_circ_43552,RMVar_hsa_circ_332811,RMVar_hsa_circ_279455,RMVar_hsa_circ_24753,RMVar_hsa_circ_9614,RMVar_hsa_circ_13121,RMVar_hsa_circ_7584,RMVar_hsa_circ_326390,RMVar_hsa_circ_133727 13399 RMVar_ID_13399 Human_SNP_ID_16846866 A-to-I Human chr1 + 66630837 66630837 66630837 AAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA AAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGATAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAA A T SGIP1 Ensembl:ENSG00000118473 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs190325446 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4541,RMVar_hsa_circ_43552,RMVar_hsa_circ_332811,RMVar_hsa_circ_279455,RMVar_hsa_circ_24753,RMVar_hsa_circ_9614,RMVar_hsa_circ_13121,RMVar_hsa_circ_7584,RMVar_hsa_circ_326390,RMVar_hsa_circ_133727 13400 RMVar_ID_13400 Human_SNP_ID_16916951 A-to-I Human chr1 - 66911877 66911876 66911878 AGATTGAGCCACTGCACTCCAGCCTGGGCAACAGAGTGAGACTCTGTCTCAAAGAAAAGAAAAAA AGATTGAGCCACTGCACTCCAGCCTGGGCAA__GAGTGAGACTCTGTCTCAAAGAAAAGAAAAAA CTG C WDR78 Ensembl:ENSG00000152763 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1190879396 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_265454 13401 RMVar_ID_13401 Human_SNP_ID_16919591 A-to-I Human chr1 - 66923254 66923254 66923254 TGTACACCTAAGCTATAGTAGGCTATACATCTAGGTTTGTGTAAGTACACTAAATGGTGTTTGCA TGTACACCTAAGCTATAGTAGGCTATACATCTGGGTTTGTGTAAGTACACTAAATGGTGTTTGCA T C WDR78 Ensembl:ENSG00000152763 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs958519620 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265454 13402 RMVar_ID_13402 Human_SNP_ID_16919592 A-to-I Human chr1 - 66923254 66923254 66923254 TGTACACCTAAGCTATAGTAGGCTATACATCTAGGTTTGTGTAAGTACACTAAATGGTGTTTGCA TGTACACCTAAGCTATAGTAGGCTATACATCTCGGTTTGTGTAAGTACACTAAATGGTGTTTGCA T G WDR78 Ensembl:ENSG00000152763 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs958519620 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265454 13403 RMVar_ID_13403 Human_SNP_ID_16919598 A-to-I Human chr1 - 66923267 66923267 66923267 TTGTATAGTAGACTGTACACCTAAGCTATAGTAGGCTATACATCTAGGTTTGTGTAAGTACACTA TTGTATAGTAGACTGTACACCTAAGCTATAGTGGGCTATACATCTAGGTTTGTGTAAGTACACTA T C WDR78 Ensembl:ENSG00000152763 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1381038397 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265454 13404 RMVar_ID_13404 Human_SNP_ID_16919599 A-to-I Human chr1 - 66923270 66923270 66923270 CAATTGTATAGTAGACTGTACACCTAAGCTATAGTAGGCTATACATCTAGGTTTGTGTAAGTACA CAATTGTATAGTAGACTGTACACCTAAGCTATGGTAGGCTATACATCTAGGTTTGTGTAAGTACA T C WDR78 Ensembl:ENSG00000152763 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1178193391 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265454 13405 RMVar_ID_13405 Human_SNP_ID_16928337 A-to-I Human chr1 + 66956300 66956300 66956300 AAAATTAGCCAGGCATGGTGGTGCACATGTATAGTCCCAGATACTTGGGAGGCTGAGGTGGGAGG AAAATTAGCCAGGCATGGTGGTGCACATGTATCGTCCCAGATACTTGGGAGGCTGAGGTGGGAGG A C MIER1 Ensembl:ENSG00000198160 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1384804025 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17064,RMVar_hsa_circ_133758,RMVar_hsa_circ_308823,RMVar_hsa_circ_64259,RMVar_hsa_circ_360929,RMVar_hsa_circ_360706,RMVar_hsa_circ_310192,RMVar_hsa_circ_315041,RMVar_hsa_circ_55265,RMVar_hsa_circ_292514,RMVar_hsa_circ_133759,RMVar_hsa_circ_133760 13406 RMVar_ID_13406 Human_SNP_ID_16930455 A-to-I Human chr1 + 66964552 66964552 66964552 TCGGCTCACTGCAACTTTCGCCTCTCAGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCCAAGTAGC TCGGCTCACTGCAACTTTCGCCTCTCAGGTTCGAGCAGTTCTCCTGCCTCAGCCTCCCAAGTAGC A G MIER1 Ensembl:ENSG00000198160 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1177017396 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17756559 RMVar_hsa_circ_308823,RMVar_hsa_circ_64259,RMVar_hsa_circ_360929,RMVar_hsa_circ_55265,RMVar_hsa_circ_133760,RMVar_hsa_circ_18517,RMVar_hsa_circ_133761,RMVar_hsa_circ_133764,RMVar_hsa_circ_316708,RMVar_hsa_circ_366181 13407 RMVar_ID_13407 Human_SNP_ID_17037932 A-to-I Human chr1 - 67409006 67409006 67409006 GGGAGGTGGGGGTTGCAGTGAGCCAAGATCATAGCACTGTACTCCAGTCTGGGTGACACACTGTC GGGAGGTGGGGGTTGCAGTGAGCCAAGATCATGGCACTGTACTCCAGTCTGGGTGACACACTGTC T C SERBP1 Ensembl:ENSG00000142864 Protein coding 3'UTR GSE38233;GSE100210;GSE112787 cultured B-cells;HepG2 cell line;293 Flip-In T-REx cells,empty vector - 24183664,29129909,29967493 RNA-Seq:(High) rs3208131 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5911790,Human_RBP_ID_8751512,Human_RBP_ID_11084532,Human_RBP_ID_19401620,Human_RBP_ID_23303691,Human_RBP_ID_23409569 Human_miRNA_ID_1509923,Human_miRNA_ID_1640245 13408 RMVar_ID_13408 Human_SNP_ID_17037933 A-to-I Human chr1 - 67409008 67409008 67409008 CCGGGAGGTGGGGGTTGCAGTGAGCCAAGATCATAGCACTGTACTCCAGTCTGGGTGACACACTG CCGGGAGGTGGGGGTTGCAGTGAGCCAAGATCTTAGCACTGTACTCCAGTCTGGGTGACACACTG T A SERBP1 Ensembl:ENSG00000142864 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1451128422 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5911790,Human_RBP_ID_23303691,Human_RBP_ID_23409569,Human_RBP_ID_24722060 Human_miRNA_ID_1509923 13409 RMVar_ID_13409 Human_SNP_ID_17037934 A-to-I Human chr1 - 67409013 67409013 67409013 TGAACCCGGGAGGTGGGGGTTGCAGTGAGCCAAGATCATAGCACTGTACTCCAGTCTGGGTGACA TGAACCCGGGAGGTGGGGGTTGCAGTGAGCCAGGATCATAGCACTGTACTCCAGTCTGGGTGACA T C SERBP1 Ensembl:ENSG00000142864 Protein coding 3'UTR GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,29796672,31158229,32596459,32596459 RNA-Seq:(High) rs911664406 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4098646,Human_RBP_ID_23303691,Human_RBP_ID_23409569 13410 RMVar_ID_13410 Human_SNP_ID_17037941 A-to-I Human chr1 - 67409048 67409048 67409048 TTTACAGGTGTACACCACCACACCCAAGAATCACTTGAACCCGGGAGGTGGGGGTTGCAGTGAGC TTTACAGGTGTACACCACCACACCCAAGAATCGCTTGAACCCGGGAGGTGGGGGTTGCAGTGAGC T C SERBP1 Ensembl:ENSG00000142864 Protein coding 3'UTR GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,29796672,31158229,31158229,32596459 RNA-Seq:(High) rs1001619199 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8317568,Human_RBP_ID_11084533,Human_RBP_ID_17756715,Human_RBP_ID_22785716 Human_miRNA_ID_194636,Human_miRNA_ID_695310,Human_miRNA_ID_700254,Human_miRNA_ID_1459885 13411 RMVar_ID_13411 Human_SNP_ID_17039252 A-to-I Human chr1 - 67413909 67413909 67413909 CTAGCTACTTGGGAGGCTGAGGCACAAGAATCACCTGAACCCAGGAGGTGGAGGTTGCAGTGAAC CTAGCTACTTGGGAGGCTGAGGCACAAGAATCGCCTGAACCCAGGAGGTGGAGGTTGCAGTGAAC T C SERBP1 Ensembl:ENSG00000142864 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1050758885 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11084808 13412 RMVar_ID_13412 Human_SNP_ID_17039261 A-to-I Human chr1 - 67413935 67413935 67413935 CAGGTGTGGTGGCACATCCCTGTAACCTAGCTACTTGGGAGGCTGAGGCACAAGAATCACCTGAA CAGGTGTGGTGGCACATCCCTGTAACCTAGCTGCTTGGGAGGCTGAGGCACAAGAATCACCTGAA T C SERBP1 Ensembl:ENSG00000142864 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs942201500 Functional Loss SNV dbSNP153 33..33 33 - - - 13413 RMVar_ID_13413 Human_SNP_ID_17039278 A-to-I Human chr1 - 67414008 67414008 67414008 GGGTGAACAGATCACCTGAGGTTGGGAATTTGAGACCAGCCTGGCCAACGTTGTGAAACCCTGTC GGGTGAACAGATCACCTGAGGTTGGGAATTTGCGACCAGCCTGGCCAACGTTGTGAAACCCTGTC T G SERBP1 Ensembl:ENSG00000142864 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1448956275 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22785747,Human_RBP_ID_24722131 13414 RMVar_ID_13414 Human_SNP_ID_17040518 A-to-I Human chr1 - 67418255 67418253 67418255 ACACGTGGTTTCAGCCAGGCGCAGTGGCTCACACCTGTAATCCCAGCACTTTTGGGAGACTGAGG ACACGTGGTTTCAGCCAGGCGCAGTGGCTCAC__CTGTAATCCCAGCACTTTTGGGAGACTGAGG GGT G SERBP1 Ensembl:ENSG00000142864 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs923911450 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_57862,RMVar_hsa_circ_118497,RMVar_hsa_circ_356432,RMVar_hsa_circ_67737,RMVar_hsa_circ_133777,RMVar_hsa_circ_54229 13415 RMVar_ID_13415 Human_SNP_ID_17040519 A-to-I Human chr1 - 67418255 67418255 67418255 ACACGTGGTTTCAGCCAGGCGCAGTGGCTCACACCTGTAATCCCAGCACTTTTGGGAGACTGAGG ACACGTGGTTTCAGCCAGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTTTTGGGAGACTGAGG T C SERBP1 Ensembl:ENSG00000142864 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1272918689 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57862,RMVar_hsa_circ_118497,RMVar_hsa_circ_356432,RMVar_hsa_circ_67737,RMVar_hsa_circ_133777,RMVar_hsa_circ_54229 13416 RMVar_ID_13416 Human_SNP_ID_17209616 A-to-I Human chr1 - 68114792 68114792 68114792 GCTTTACCCTATTCCAGAAGGAATAAGCCCATAGTATGATAACTGGCAGTTTTGCTAAGGCACAA GCTTTACCCTATTCCAGAAGGAATAAGCCCATTGTATGATAACTGGCAGTTTTGCTAAGGCACAA T A WLS Ensembl:ENSG00000116729 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973109404 Functional Loss SNV dbSNP153 33..33 33 - - - 13417 RMVar_ID_13417 Human_SNP_ID_17606190 A-to-I Human chr1 - 69731456 69731456 69731456 AATAGTAAGTTTATACTTGATATGGTTGGGCTATATCTCCACCCAAATCTTATCTTGAATTGTAG AATAGTAAGTTTATACTTGATATGGTTGGGCTGTATCTCCACCCAAATCTTATCTTGAATTGTAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1302157373 Functional Loss SNV dbSNP153 33..33 33 - - - 13418 RMVar_ID_13418 Human_SNP_ID_17693714 A-to-I Human chr1 + 70101562 70101562 70101562 TGTTAAATGTTGGCCTTGTAAACTAACTTTCTAAGTCCTTTAAGGTTTATGTCCAGGGATGTAGA TGTTAAATGTTGGCCTTGTAAACTAACTTTCTGAGTCCTTTAAGGTTTATGTCCAGGGATGTAGA A G LRRC7 Ensembl:ENSG00000033122 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1473232826 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_342337,RMVar_hsa_circ_133829,RMVar_hsa_circ_531,RMVar_hsa_circ_133827,RMVar_hsa_circ_323289,RMVar_hsa_circ_133830,RMVar_hsa_circ_133838,RMVar_hsa_circ_133834,RMVar_hsa_circ_133828,RMVar_hsa_circ_270435,RMVar_hsa_circ_133839,RMVar_hsa_circ_133837,RMVar_hsa_circ_301005,RMVar_hsa_circ_268797,RMVar_hsa_circ_133840,RMVar_hsa_circ_133842,RMVar_hsa_circ_133841,RMVar_hsa_circ_133845,RMVar_hsa_circ_133846 13419 RMVar_ID_13419 Human_SNP_ID_17707355 A-to-I Human chr1 - 70161468 70161468 70161468 CTTGCACTGCAAGCTCCGCCTCCCGGCTTCACACCATTCTCCTGCCTCAGCCTCCCTAGTAGCTG CTTGCACTGCAAGCTCCGCCTCCCGGCTTCACGCCATTCTCCTGCCTCAGCCTCCCTAGTAGCTG T C LRRC40 Ensembl:ENSG00000066557 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232172589 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1334,RMVar_hsa_circ_107812,RMVar_hsa_circ_133850,RMVar_hsa_circ_133852,RMVar_hsa_circ_325299,RMVar_hsa_circ_133854,RMVar_hsa_circ_303498,RMVar_hsa_circ_133855,RMVar_hsa_circ_35227,RMVar_hsa_circ_133858,RMVar_hsa_circ_334756,RMVar_hsa_circ_369478 13420 RMVar_ID_13420 Human_SNP_ID_17708486 A-to-I Human chr1 - 70166541 70166541 70166541 GCAATCCTTGTGCCTCAGCCTTCCAAGTAGCTAGGATTACAGGTGTGCACCACTACACCAGGCTA GCAATCCTTGTGCCTCAGCCTTCCAAGTAGCTGGGATTACAGGTGTGCACCACTACACCAGGCTA T C LRRC40 Ensembl:ENSG00000066557 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251977427 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1334,RMVar_hsa_circ_107812,RMVar_hsa_circ_133850,RMVar_hsa_circ_133852,RMVar_hsa_circ_325299,RMVar_hsa_circ_133854,RMVar_hsa_circ_303498,RMVar_hsa_circ_133855,RMVar_hsa_circ_35227,RMVar_hsa_circ_133858,RMVar_hsa_circ_334756,RMVar_hsa_circ_369478 13421 RMVar_ID_13421 Human_SNP_ID_17719006 A-to-I Human chr1 + 70210526 70210526 70210526 CATGAGTTCAGGAGTTAGAGACCAGCCTGGACAATATCTTGAAACTCTGTCTCTACAAAAAATAC CATGAGTTCAGGAGTTAGAGACCAGCCTGGACCATATCTTGAAACTCTGTCTCTACAAAAAATAC A C SRSF11 Ensembl:ENSG00000116754 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1014448972 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11094122 RMVar_hsa_circ_109937,RMVar_hsa_circ_133867,RMVar_hsa_circ_106740,RMVar_hsa_circ_133866 13422 RMVar_ID_13422 Human_SNP_ID_17719007 A-to-I Human chr1 + 70210526 70210526 70210526 CATGAGTTCAGGAGTTAGAGACCAGCCTGGACAATATCTTGAAACTCTGTCTCTACAAAAAATAC CATGAGTTCAGGAGTTAGAGACCAGCCTGGACGATATCTTGAAACTCTGTCTCTACAAAAAATAC A G SRSF11 Ensembl:ENSG00000116754 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1014448972 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11094122 RMVar_hsa_circ_109937,RMVar_hsa_circ_133867,RMVar_hsa_circ_106740,RMVar_hsa_circ_133866 13423 RMVar_ID_13423 Human_SNP_ID_17719015 A-to-I Human chr1 + 70210561 70210561 70210561 ATCTTGAAACTCTGTCTCTACAAAAAATACAAAAATTACCTGGGTGTGGTGTGGCATGCACCTGT ATCTTGAAACTCTGTCTCTACAAAAAATACAAGAATTACCTGGGTGTGGTGTGGCATGCACCTGT A G SRSF11 Ensembl:ENSG00000116754 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1331352226 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109937,RMVar_hsa_circ_133867,RMVar_hsa_circ_106740,RMVar_hsa_circ_133866 13424 RMVar_ID_13424 Human_SNP_ID_17719016 A-to-I Human chr1 + 70210566 70210566 70210566 GAAACTCTGTCTCTACAAAAAATACAAAAATTACCTGGGTGTGGTGTGGCATGCACCTGTGATCC GAAACTCTGTCTCTACAAAAAATACAAAAATTGCCTGGGTGTGGTGTGGCATGCACCTGTGATCC A G SRSF11 Ensembl:ENSG00000116754 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1302716038 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109937,RMVar_hsa_circ_133867,RMVar_hsa_circ_106740,RMVar_hsa_circ_133866 13425 RMVar_ID_13425 Human_SNP_ID_17720371 A-to-I Human chr1 + 70216481 70216481 70216481 TTGAGATAAGGTCTCACTCTGTCACCCAGACTAGAGTACAGTGTCACGATCTCAGCTCACTGCAG TTGAGATAAGGTCTCACTCTGTCACCCAGACTGGAGTACAGTGTCACGATCTCAGCTCACTGCAG A G SRSF11 Ensembl:ENSG00000116754 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1415713230 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11094368 RMVar_hsa_circ_109937,RMVar_hsa_circ_133867,RMVar_hsa_circ_106740,RMVar_hsa_circ_133866 13426 RMVar_ID_13426 Human_SNP_ID_17738871 A-to-I Human chr1 - 70290620 70290620 70290620 GGATGATCACTTGAGCCCGGGAGACTGAGGCTACAATGAGCTATAATCATGCCACTGCCACTGCA GGATGATCACTTGAGCCCGGGAGACTGAGGCTGCAATGAGCTATAATCATGCCACTGCCACTGCA T C ANKRD13C Ensembl:ENSG00000118454 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1138751 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11096529 RMVar_hsa_circ_40086,RMVar_hsa_circ_277514,RMVar_hsa_circ_335935,RMVar_hsa_circ_279275,RMVar_hsa_circ_302197,RMVar_hsa_circ_277884,RMVar_hsa_circ_273269,RMVar_hsa_circ_40650,RMVar_hsa_circ_133882,RMVar_hsa_circ_133884,RMVar_hsa_circ_133885,RMVar_hsa_circ_133883,RMVar_hsa_circ_133889,RMVar_hsa_circ_321500,RMVar_hsa_circ_361516,RMVar_hsa_circ_133881,RMVar_hsa_circ_341044,RMVar_hsa_circ_313771,RMVar_hsa_circ_70253,RMVar_hsa_circ_277759,RMVar_hsa_circ_133891,RMVar_hsa_circ_133892,RMVar_hsa_circ_133890,RMVar_hsa_circ_358383,RMVar_hsa_circ_133888,RMVar_hsa_circ_378346,RMVar_hsa_circ_265402,RMVar_hsa_circ_280172,RMVar_hsa_circ_72624,RMVar_hsa_circ_133894 13427 RMVar_ID_13427 Human_SNP_ID_17739202 A-to-I Human chr1 - 70291996 70291996 70291996 TCCTGCCTCATCCCCGCCAGGTAGCTGGGATTACAGGCCCTGCTACCAGGCCTGGCTAATTTTTG TCCTGCCTCATCCCCGCCAGGTAGCTGGGATTGCAGGCCCTGCTACCAGGCCTGGCTAATTTTTG T C ANKRD13C Ensembl:ENSG00000118454 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1244664617 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40086,RMVar_hsa_circ_277514,RMVar_hsa_circ_335935,RMVar_hsa_circ_279275,RMVar_hsa_circ_302197,RMVar_hsa_circ_277884,RMVar_hsa_circ_273269,RMVar_hsa_circ_40650,RMVar_hsa_circ_133882,RMVar_hsa_circ_133884,RMVar_hsa_circ_133885,RMVar_hsa_circ_133883,RMVar_hsa_circ_133889,RMVar_hsa_circ_321500,RMVar_hsa_circ_361516,RMVar_hsa_circ_133881,RMVar_hsa_circ_341044,RMVar_hsa_circ_313771,RMVar_hsa_circ_70253,RMVar_hsa_circ_277759,RMVar_hsa_circ_133891,RMVar_hsa_circ_133892,RMVar_hsa_circ_133890,RMVar_hsa_circ_358383,RMVar_hsa_circ_133888,RMVar_hsa_circ_378346,RMVar_hsa_circ_265402,RMVar_hsa_circ_280172,RMVar_hsa_circ_72624,RMVar_hsa_circ_133894 13428 RMVar_ID_13428 Human_SNP_ID_17742340 A-to-I Human chr1 - 70305086 70305086 70305086 TTTTGTTTTTTCTTTTTTTAGATAATAAAGATAGGGTCTCACTATATTGCCCAGGCTGGTCTTGA TTTTGTTTTTTCTTTTTTTAGATAATAAAGATGGGGTCTCACTATATTGCCCAGGCTGGTCTTGA T C ANKRD13C Ensembl:ENSG00000118454 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1000196178 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_302197,RMVar_hsa_circ_277884,RMVar_hsa_circ_273269,RMVar_hsa_circ_40650,RMVar_hsa_circ_133882,RMVar_hsa_circ_133883,RMVar_hsa_circ_321500,RMVar_hsa_circ_133881,RMVar_hsa_circ_341044,RMVar_hsa_circ_70253,RMVar_hsa_circ_277759,RMVar_hsa_circ_133891,RMVar_hsa_circ_133892,RMVar_hsa_circ_133890,RMVar_hsa_circ_358383,RMVar_hsa_circ_378346,RMVar_hsa_circ_265402,RMVar_hsa_circ_280172,RMVar_hsa_circ_133901,RMVar_hsa_circ_133896,RMVar_hsa_circ_133894,RMVar_hsa_circ_283392,RMVar_hsa_circ_309854,RMVar_hsa_circ_284774,RMVar_hsa_circ_270255,RMVar_hsa_circ_133898,RMVar_hsa_circ_64692,RMVar_hsa_circ_133897,RMVar_hsa_circ_272623,RMVar_hsa_circ_292425,RMVar_hsa_circ_133895,RMVar_hsa_circ_328306,RMVar_hsa_circ_285308,RMVar_hsa_circ_133903,RMVar_hsa_circ_133904,RMVar_hsa_circ_133902,RMVar_hsa_circ_133908,RMVar_hsa_circ_292457,RMVar_hsa_circ_329144,RMVar_hsa_circ_315408,RMVar_hsa_circ_279863,RMVar_hsa_circ_133906,RMVar_hsa_circ_133907,RMVar_hsa_circ_133905 13429 RMVar_ID_13429 Human_SNP_ID_17742812 A-to-I Human chr1 - 70307345 70307345 70307345 TTTGATAGAGATGGGGTTTCGCCATGTTGCCCAGGCCGGTCTTGAACTCCTGGGCTCAAGCGATT TTTGATAGAGATGGGGTTTCGCCATGTTGCCCTGGCCGGTCTTGAACTCCTGGGCTCAAGCGATT T A ANKRD13C Ensembl:ENSG00000118454 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232292330 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_277884,RMVar_hsa_circ_273269,RMVar_hsa_circ_40650,RMVar_hsa_circ_133882,RMVar_hsa_circ_133881,RMVar_hsa_circ_341044,RMVar_hsa_circ_70253,RMVar_hsa_circ_277759,RMVar_hsa_circ_133891,RMVar_hsa_circ_133892,RMVar_hsa_circ_358383,RMVar_hsa_circ_265402,RMVar_hsa_circ_280172,RMVar_hsa_circ_133896,RMVar_hsa_circ_133894,RMVar_hsa_circ_283392,RMVar_hsa_circ_309854,RMVar_hsa_circ_284774,RMVar_hsa_circ_64692,RMVar_hsa_circ_133897,RMVar_hsa_circ_292425,RMVar_hsa_circ_133895,RMVar_hsa_circ_328306,RMVar_hsa_circ_285308,RMVar_hsa_circ_133903,RMVar_hsa_circ_133904,RMVar_hsa_circ_133902,RMVar_hsa_circ_26008,RMVar_hsa_circ_133908,RMVar_hsa_circ_329144,RMVar_hsa_circ_315408,RMVar_hsa_circ_279863,RMVar_hsa_circ_133906,RMVar_hsa_circ_133907,RMVar_hsa_circ_339128,RMVar_hsa_circ_293255,RMVar_hsa_circ_133909 13430 RMVar_ID_13430 Human_SNP_ID_17743296 A-to-I Human chr1 - 70309362 70309362 70309362 CTCTTCTGAAAATTGGGGAGTAGGCTGGGTGCAGTGGCTCACGCCGTAATCCCAGCACTTTGGGA CTCTTCTGAAAATTGGGGAGTAGGCTGGGTGCGGTGGCTCACGCCGTAATCCCAGCACTTTGGGA T C ANKRD13C Ensembl:ENSG00000118454 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1180283573 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_277884,RMVar_hsa_circ_273269,RMVar_hsa_circ_40650,RMVar_hsa_circ_133882,RMVar_hsa_circ_133881,RMVar_hsa_circ_341044,RMVar_hsa_circ_70253,RMVar_hsa_circ_277759,RMVar_hsa_circ_133891,RMVar_hsa_circ_133892,RMVar_hsa_circ_358383,RMVar_hsa_circ_265402,RMVar_hsa_circ_280172,RMVar_hsa_circ_133896,RMVar_hsa_circ_133894,RMVar_hsa_circ_283392,RMVar_hsa_circ_309854,RMVar_hsa_circ_284774,RMVar_hsa_circ_64692,RMVar_hsa_circ_133897,RMVar_hsa_circ_292425,RMVar_hsa_circ_133895,RMVar_hsa_circ_328306,RMVar_hsa_circ_285308,RMVar_hsa_circ_133903,RMVar_hsa_circ_133904,RMVar_hsa_circ_133902,RMVar_hsa_circ_26008,RMVar_hsa_circ_133908,RMVar_hsa_circ_329144,RMVar_hsa_circ_315408,RMVar_hsa_circ_279863,RMVar_hsa_circ_133906,RMVar_hsa_circ_133907,RMVar_hsa_circ_339128,RMVar_hsa_circ_293255,RMVar_hsa_circ_133909 13431 RMVar_ID_13431 Human_SNP_ID_17743350 A-to-I Human chr1 - 70309524 70309524 70309524 TTAGTACAGACGGGATTTCACCGTGTTAGCCAAGATGGTCTTGATCTTCTCACCTCGTGATCCAC TTAGTACAGACGGGATTTCACCGTGTTAGCCACGATGGTCTTGATCTTCTCACCTCGTGATCCAC T G ANKRD13C Ensembl:ENSG00000118454 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1206513211 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_277884,RMVar_hsa_circ_273269,RMVar_hsa_circ_40650,RMVar_hsa_circ_133882,RMVar_hsa_circ_133881,RMVar_hsa_circ_341044,RMVar_hsa_circ_70253,RMVar_hsa_circ_277759,RMVar_hsa_circ_133891,RMVar_hsa_circ_133892,RMVar_hsa_circ_358383,RMVar_hsa_circ_265402,RMVar_hsa_circ_280172,RMVar_hsa_circ_133896,RMVar_hsa_circ_133894,RMVar_hsa_circ_283392,RMVar_hsa_circ_309854,RMVar_hsa_circ_284774,RMVar_hsa_circ_64692,RMVar_hsa_circ_133897,RMVar_hsa_circ_292425,RMVar_hsa_circ_133895,RMVar_hsa_circ_328306,RMVar_hsa_circ_285308,RMVar_hsa_circ_133903,RMVar_hsa_circ_133904,RMVar_hsa_circ_133902,RMVar_hsa_circ_26008,RMVar_hsa_circ_133908,RMVar_hsa_circ_329144,RMVar_hsa_circ_315408,RMVar_hsa_circ_279863,RMVar_hsa_circ_133906,RMVar_hsa_circ_133907,RMVar_hsa_circ_339128,RMVar_hsa_circ_293255,RMVar_hsa_circ_133909 13432 RMVar_ID_13432 Human_SNP_ID_17743391 A-to-I Human chr1 - 70309669 70309669 70309669 CTCTGTCGCCCAGGCTAGCGCGATCTCGGCTCACTGCAAGCTCCACCTCCTGGGTTCACGCCATT CTCTGTCGCCCAGGCTAGCGCGATCTCGGCTCGCTGCAAGCTCCACCTCCTGGGTTCACGCCATT T C ANKRD13C Ensembl:ENSG00000118454 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1159197081 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_277884,RMVar_hsa_circ_273269,RMVar_hsa_circ_40650,RMVar_hsa_circ_133882,RMVar_hsa_circ_133881,RMVar_hsa_circ_341044,RMVar_hsa_circ_70253,RMVar_hsa_circ_277759,RMVar_hsa_circ_133891,RMVar_hsa_circ_133892,RMVar_hsa_circ_358383,RMVar_hsa_circ_265402,RMVar_hsa_circ_280172,RMVar_hsa_circ_133896,RMVar_hsa_circ_133894,RMVar_hsa_circ_283392,RMVar_hsa_circ_309854,RMVar_hsa_circ_284774,RMVar_hsa_circ_64692,RMVar_hsa_circ_133897,RMVar_hsa_circ_292425,RMVar_hsa_circ_133895,RMVar_hsa_circ_328306,RMVar_hsa_circ_285308,RMVar_hsa_circ_133903,RMVar_hsa_circ_133904,RMVar_hsa_circ_133902,RMVar_hsa_circ_26008,RMVar_hsa_circ_133908,RMVar_hsa_circ_329144,RMVar_hsa_circ_315408,RMVar_hsa_circ_279863,RMVar_hsa_circ_133906,RMVar_hsa_circ_133907,RMVar_hsa_circ_339128,RMVar_hsa_circ_293255,RMVar_hsa_circ_133909 13433 RMVar_ID_13433 Human_SNP_ID_17745608 A-to-I Human chr1 - 70319361 70319361 70319361 CCTCAGGCAATCCACCCGGCTCGGCCTCCCAAAGTGCTGAGATTACAGGTGTGAGCCACCGTGCC CCTCAGGCAATCCACCCGGCTCGGCCTCCCAATGTGCTGAGATTACAGGTGTGAGCCACCGTGCC T A ANKRD13C Ensembl:ENSG00000118454 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1317778878 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_277884,RMVar_hsa_circ_133881,RMVar_hsa_circ_70253,RMVar_hsa_circ_133892,RMVar_hsa_circ_358383,RMVar_hsa_circ_283392,RMVar_hsa_circ_64692,RMVar_hsa_circ_292425,RMVar_hsa_circ_133895,RMVar_hsa_circ_133904,RMVar_hsa_circ_133908,RMVar_hsa_circ_315408,RMVar_hsa_circ_339128,RMVar_hsa_circ_348247 13434 RMVar_ID_13434 Human_SNP_ID_17745651 A-to-I Human chr1 - 70319525 70319525 70319525 TTGGCTCTCTGCAGCCTCCGCCTCTCAGATTCAAGCAATTCTCCTGCCCCAGTCTCCCGAGTAGC TTGGCTCTCTGCAGCCTCCGCCTCTCAGATTCCAGCAATTCTCCTGCCCCAGTCTCCCGAGTAGC T G ANKRD13C Ensembl:ENSG00000118454 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs940213165 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24724712 RMVar_hsa_circ_277884,RMVar_hsa_circ_133881,RMVar_hsa_circ_70253,RMVar_hsa_circ_133892,RMVar_hsa_circ_358383,RMVar_hsa_circ_283392,RMVar_hsa_circ_64692,RMVar_hsa_circ_292425,RMVar_hsa_circ_133895,RMVar_hsa_circ_133904,RMVar_hsa_circ_133908,RMVar_hsa_circ_315408,RMVar_hsa_circ_339128,RMVar_hsa_circ_348247 13435 RMVar_ID_13435 Human_SNP_ID_17745664 A-to-I Human chr1 - 70319568 70319568 70319568 AGTTTCCCTCTTGTTGCTCAGGCTGGAATGCAATGGCGCGATCTTGGCTCTCTGCAGCCTCCGCC AGTTTCCCTCTTGTTGCTCAGGCTGGAATGCAGTGGCGCGATCTTGGCTCTCTGCAGCCTCCGCC T C ANKRD13C Ensembl:ENSG00000118454 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs552764436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11097204 RMVar_hsa_circ_277884,RMVar_hsa_circ_133881,RMVar_hsa_circ_70253,RMVar_hsa_circ_133892,RMVar_hsa_circ_358383,RMVar_hsa_circ_283392,RMVar_hsa_circ_64692,RMVar_hsa_circ_292425,RMVar_hsa_circ_133895,RMVar_hsa_circ_133904,RMVar_hsa_circ_133908,RMVar_hsa_circ_315408,RMVar_hsa_circ_339128,RMVar_hsa_circ_348247 13436 RMVar_ID_13436 Human_SNP_ID_17745997 A-to-I Human chr1 - 70320976 70320976 70320976 TGCTTGAGCCTGGGAAACATAGGGGGACCCCAACACTACAAAAAGTACAAAAATTAGCTGGTGTG TGCTTGAGCCTGGGAAACATAGGGGGACCCCAGCACTACAAAAAGTACAAAAATTAGCTGGTGTG T C ANKRD13C Ensembl:ENSG00000118454 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs575569516 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_277884,RMVar_hsa_circ_133881,RMVar_hsa_circ_70253,RMVar_hsa_circ_133892,RMVar_hsa_circ_358383,RMVar_hsa_circ_283392,RMVar_hsa_circ_64692,RMVar_hsa_circ_292425,RMVar_hsa_circ_133895,RMVar_hsa_circ_133904,RMVar_hsa_circ_133908,RMVar_hsa_circ_315408,RMVar_hsa_circ_339128,RMVar_hsa_circ_348247 13437 RMVar_ID_13437 Human_SNP_ID_17746372 A-to-I Human chr1 - 70322747 70322747 70322747 GTCAGGTGATCCACCAGCCTCGGCCTCCCAAAATGCTGGGGTTACAGGTGTGAGCCACTGCGCCC GTCAGGTGATCCACCAGCCTCGGCCTCCCAAAGTGCTGGGGTTACAGGTGTGAGCCACTGCGCCC T C ANKRD13C Ensembl:ENSG00000118454 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1173407040 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_277884,RMVar_hsa_circ_133881,RMVar_hsa_circ_70253,RMVar_hsa_circ_133892,RMVar_hsa_circ_358383,RMVar_hsa_circ_283392,RMVar_hsa_circ_64692,RMVar_hsa_circ_292425,RMVar_hsa_circ_133895,RMVar_hsa_circ_133904,RMVar_hsa_circ_133908,RMVar_hsa_circ_315408,RMVar_hsa_circ_339128,RMVar_hsa_circ_348247 13438 RMVar_ID_13438 Human_SNP_ID_17750361 A-to-I Human chr1 - 70339101 70339101 70339101 GACTCAAGCGATTCTTCTACTTCGGCTTCCCAAGCAGCTGGATTACAGGGTGCGCTACCACACCC GACTCAAGCGATTCTTCTACTTCGGCTTCCCAGGCAGCTGGATTACAGGGTGCGCTACCACACCC T C ANKRD13C Ensembl:ENSG00000118454 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1389599497 Functional Loss SNV dbSNP153 33..33 33 - - - 13439 RMVar_ID_13439 Human_SNP_ID_17753382 A-to-I Human chr1 - 70351575 70351575 70351575 ACCAACATAGTGAAACCCCGTCTCTACTGAAAATATGAAAATTAGCCTGGCATGGTGGTGCATGC ACCAACATAGTGAAACCCCGTCTCTACTGAAAGTATGAAAATTAGCCTGGCATGGTGGTGCATGC T C ANKRD13C Ensembl:ENSG00000118454 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1464343711 Functional Loss SNV dbSNP153 33..33 33 - - - 13440 RMVar_ID_13440 Human_SNP_ID_17753385 A-to-I Human chr1 - 70351582 70351582 70351582 CAGCCTGACCAACATAGTGAAACCCCGTCTCTACTGAAAATATGAAAATTAGCCTGGCATGGTGG CAGCCTGACCAACATAGTGAAACCCCGTCTCTGCTGAAAATATGAAAATTAGCCTGGCATGGTGG T C ANKRD13C Ensembl:ENSG00000118454 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1430870201 Functional Loss SNV dbSNP153 33..33 33 - - - 13441 RMVar_ID_13441 Human_SNP_ID_17753391 A-to-I Human chr1 - 70351599 70351598 70351600 GGTCAGGAGTTCAAGACCAGCCTGACCAACATAGTGAAACCCCGTCTCTACTGAAAATATGAAAA GGTCAGGAGTTCAAGACCAGCCTGACCAACA__GTGAAACCCCGTCTCTACTGAAAATATGAAAA CTA C ANKRD13C Ensembl:ENSG00000118454 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1197021768 Functional Loss DEL dbSNP153 32..33 33 - - - 13442 RMVar_ID_13442 Human_SNP_ID_17755315 A-to-I Human chr1 + 70358546 70358545 70358546 CTGGGTTTGGCCATGTCACCCAGGCTAGTCTCAAACTCCTGGACTCAAGCCATCTACCCACCTCG CTGGGTTTGGCCATGTCACCCAGGCTAGTCTC_AACTCCTGGACTCAAGCCATCTACCCACCTCG CA C HHLA3 Ensembl:ENSG00000197568 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1374528138 Functional Loss DEL dbSNP153 33..33 33 - - - 13443 RMVar_ID_13443 Human_SNP_ID_17757026 A-to-I Human chr1 + 70365863 70365863 70365863 TTTGGTCTCAGCAAGCCAGACATTTCCTTTCTATTGATCCCAGGTATTTAGATAAACTCAACCGT TTTGGTCTCAGCAAGCCAGACATTTCCTTTCTGTTGATCCCAGGTATTTAGATAAACTCAACCGT A G HHLA3 Ensembl:ENSG00000197568 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1025946849 Functional Loss SNV dbSNP153 33..33 33 - - - 13444 RMVar_ID_13444 Human_SNP_ID_17757029 A-to-I Human chr1 + 70365872 70365872 70365872 AGCAAGCCAGACATTTCCTTTCTATTGATCCCAGGTATTTAGATAAACTCAACCGTCAACCAGAA AGCAAGCCAGACATTTCCTTTCTATTGATCCCGGGTATTTAGATAAACTCAACCGTCAACCAGAA A G HHLA3 Ensembl:ENSG00000197568 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1238606795 Functional Loss SNV dbSNP153 33..33 33 - - - 13445 RMVar_ID_13445 Human_SNP_ID_17768320 A-to-I Human chr1 + 70415297 70415297 70415297 ATGGTGACATGCACCTGTAGTCTTAGCTACTCAGGAGGCTGAGATCGGAGGATTGCTTAAGCCCA ATGGTGACATGCACCTGTAGTCTTAGCTACTCTGGAGGCTGAGATCGGAGGATTGCTTAAGCCCA A T CTH Ensembl:ENSG00000116761 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978650146 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5860900 13446 RMVar_ID_13446 Human_SNP_ID_17775321 A-to-I Human chr1 + 70444963 70444963 70444963 GCAGATTCTTCCTCTGTTACCCAGGTTGGAGTACAGTGGCACGATCTCCAGTCACTGCAACCTCT GCAGATTCTTCCTCTGTTACCCAGGTTGGAGTTCAGTGGCACGATCTCCAGTCACTGCAACCTCT A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1405140579 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8318360 13447 RMVar_ID_13447 Human_SNP_ID_17775337 A-to-I Human chr1 + 70445009 70445009 70445009 TCCAGTCACTGCAACCTCTGCCTCCCAGGTTCAAGCTATTCTCCTGCCTCAGCCTCACGAGTAGC TCCAGTCACTGCAACCTCTGCCTCCCAGGTTCCAGCTATTCTCCTGCCTCAGCCTCACGAGTAGC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910604715 Functional Loss SNV dbSNP153 33..33 33 - - - 13448 RMVar_ID_13448 Human_SNP_ID_18046182 A-to-I Human chr1 - 71567977 71567975 71567977 TGGTTTATTAACAACAGAAATTTACTTCTTATAGTTTTGGAGACTGAAAGTCTGAGATTAAGATG TGGTTTATTAACAACAGAAATTTACTTCTTAT__TTTTGGAGACTGAAAGTCTGAGATTAAGATG ACT A NEGR1 Ensembl:ENSG00000172260 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1557570023 Functional Loss DEL dbSNP153 33..34 33 - - - 13449 RMVar_ID_13449 Human_SNP_ID_18075195 A-to-I Human chr1 - 71685385 71685385 71685385 CCAGGAGGCGGAGTTTGCAGTGAGCCAAGATCATGCCATTGCACTCCAGCCTGGGCAAAAAGAGT CCAGGAGGCGGAGTTTGCAGTGAGCCAAGATCCTGCCATTGCACTCCAGCCTGGGCAAAAAGAGT T G NEGR1 Ensembl:ENSG00000172260 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1417101875 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15617,RMVar_hsa_circ_334592 13450 RMVar_ID_13450 Human_SNP_ID_18075229 A-to-I Human chr1 - 71685510 71685510 71685510 CAAGAGCAGGCTGGCCAATATGGTGAAACCCCATCTTTACTAAAAATACAAAAGTAGCCAGGTGT CAAGAGCAGGCTGGCCAATATGGTGAAACCCCTTCTTTACTAAAAATACAAAAGTAGCCAGGTGT T A NEGR1 Ensembl:ENSG00000172260 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1031847773 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15617,RMVar_hsa_circ_334592 13451 RMVar_ID_13451 Human_SNP_ID_18178939 A-to-I Human chr1 - 72093183 72093183 72093183 GGGACTACAGGCATGCACCACCATGCTCAGCTAATTTTTATATTTTTATAAGGGACAGAGTTTCA GGGACTACAGGCATGCACCACCATGCTCAGCTGATTTTTATATTTTTATAAGGGACAGAGTTTCA T C NEGR1 Ensembl:ENSG00000172260 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1451854789 Functional Loss SNV dbSNP153 33..33 33 - - - 13452 RMVar_ID_13452 Human_SNP_ID_18183181 A-to-I Human chr1 - 72110181 72110181 72110181 CTAAGTTTTAGGGTACATGTGCACATTGTGCAAGTTAGTTACATATGCATTGCTGGTGGAAATTA CTAAGTTTTAGGGTACATGTGCACATTGTGCAGGTTAGTTACATATGCATTGCTGGTGGAAATTA T C NEGR1 Ensembl:ENSG00000172260 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1380937708 Functional Loss SNV dbSNP153 33..33 33 - - - 13453 RMVar_ID_13453 Human_SNP_ID_18186234 A-to-I Human chr1 - 72121866 72121866 72121866 ATTTTTTAATTGATATGTTGTCATATAAATTTAAAAAAAGATGATCAGTAATGGAGGTGCTAACA ATTTTTTAATTGATATGTTGTCATATAAATTTTAAAAAAGATGATCAGTAATGGAGGTGCTAACA T A NEGR1 Ensembl:ENSG00000172260 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs949448943 Functional Loss SNV dbSNP153 33..33 33 - - - 13454 RMVar_ID_13454 Human_SNP_ID_18196649 A-to-I Human chr1 - 72162399 72162399 72162399 TGCAGTGGCACGATCTCGGCTGGCTTACTGCAACCTCTGCCTCCCGGGTTCAAGCAATTCTGCCT TGCAGTGGCACGATCTCGGCTGGCTTACTGCATCCTCTGCCTCCCGGGTTCAAGCAATTCTGCCT T A NEGR1 Ensembl:ENSG00000172260 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1244301279 Functional Loss SNV dbSNP153 33..33 33 - - - 13455 RMVar_ID_13455 Human_SNP_ID_18196662 A-to-I Human chr1 - 72162445 72162445 72162445 GTTTGTTTGTTTGTTTGTTTGGCTTCCTCTGTAGCCTAGGCTGGAGTGCAGTGGCACGATCTCGG GTTTGTTTGTTTGTTTGTTTGGCTTCCTCTGTGGCCTAGGCTGGAGTGCAGTGGCACGATCTCGG T C NEGR1 Ensembl:ENSG00000172260 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1297050852 Functional Loss SNV dbSNP153 33..33 33 - - - 13456 RMVar_ID_13456 Human_SNP_ID_18199342 A-to-I Human chr1 - 72173267 72173267 72173267 GTGGTGGCTCATGCCTGTAATCCTAGCACTTTAGAAGGCCCAGGCTAGCAGATTGCTTGAACTCA GTGGTGGCTCATGCCTGTAATCCTAGCACTTTGGAAGGCCCAGGCTAGCAGATTGCTTGAACTCA T C NEGR1 Ensembl:ENSG00000172260 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 29129909,30559470 RNA-Seq:(High) rs774148224 Functional Loss SNV dbSNP153 33..33 33 - - - 13457 RMVar_ID_13457 Human_SNP_ID_18200794 A-to-I Human chr1 - 72178939 72178939 72178939 CAAACTATGCATCTGACAAATGTCTAATATCCAGAATCTATAAGCAACTCAAACAAATTAACAAG CAAACTATGCATCTGACAAATGTCTAATATCCGGAATCTATAAGCAACTCAAACAAATTAACAAG T C NEGR1 Ensembl:ENSG00000172260 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1332666972 Functional Loss SNV dbSNP153 33..33 33 - - - 13458 RMVar_ID_13458 Human_SNP_ID_18200906 A-to-I Human chr1 - 72179393 72179393 72179393 AACAAATAACTGCAGAATCTCAATAACATTCAAAACAGCATGGTATTGGAACAAAACCAGACACA AACAAATAACTGCAGAATCTCAATAACATTCAGAACAGCATGGTATTGGAACAAAACCAGACACA T C NEGR1 Ensembl:ENSG00000172260 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs903337781 Functional Loss SNV dbSNP153 33..33 33 - - - 13459 RMVar_ID_13459 Human_SNP_ID_18219725 A-to-I Human chr1 - 72255648 72255648 72255648 TACCCAGGGAGGCTGAGGCTGGGAATTGCTTGAACCCGGGAGGGCGGAGGTTGCAGTGAGCTGAG TACCCAGGGAGGCTGAGGCTGGGAATTGCTTGGACCCGGGAGGGCGGAGGTTGCAGTGAGCTGAG T C NEGR1 Ensembl:ENSG00000172260 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs977698642 Functional Loss SNV dbSNP153 33..33 33 - - - 13460 RMVar_ID_13460 Human_SNP_ID_18224306 A-to-I Human chr1 - 72274042 72274042 72274042 CTTCTGTCTCAAAATGGCTCCAAATGATTTCTATACTGCAAAATAAAGCCAAATTCTGGAAACTA CTTCTGTCTCAAAATGGCTCCAAATGATTTCTGTACTGCAAAATAAAGCCAAATTCTGGAAACTA T C NEGR1 Ensembl:ENSG00000172260 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1044217236 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26391185 13461 RMVar_ID_13461 Human_SNP_ID_18224495 A-to-I Human chr1 - 72274753 72274753 72274753 ACAGCTGGGGTCACAGATGAACTGCTTACAGCAAGCAATTTCTCCTTCCGATTTTACTCCAATTA ACAGCTGGGGTCACAGATGAACTGCTTACAGCGAGCAATTTCTCCTTCCGATTTTACTCCAATTA T C NEGR1 Ensembl:ENSG00000172260 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879069725 Functional Loss SNV dbSNP153 33..33 33 - - - 13462 RMVar_ID_13462 Human_SNP_ID_18224496 A-to-I Human chr1 - 72274753 72274753 72274753 ACAGCTGGGGTCACAGATGAACTGCTTACAGCAAGCAATTTCTCCTTCCGATTTTACTCCAATTA ACAGCTGGGGTCACAGATGAACTGCTTACAGCCAGCAATTTCTCCTTCCGATTTTACTCCAATTA T G NEGR1 Ensembl:ENSG00000172260 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879069725 Functional Loss SNV dbSNP153 33..33 33 - - - 13463 RMVar_ID_13463 Human_SNP_ID_18838756 A-to-I Human chr1 + 74750844 74750844 74750844 TTTTTTTTTTTTTGAGATAGAGTTTCACTCTTATTGCCCAGACTGTAGTGCAATGTCTCAGTCTC TTTTTTTTTTTTTGAGATAGAGTTTCACTCTTTTTGCCCAGACTGTAGTGCAATGTCTCAGTCTC A T TYW3 Ensembl:ENSG00000162623 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1297986519 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11101775 RMVar_hsa_circ_48792,RMVar_hsa_circ_334576 13464 RMVar_ID_13464 Human_SNP_ID_18842050 A-to-I Human chr1 + 74765642 74765642 74765642 AGTAAATGAAAAGAGAAGATAAATGAATAAAAAAAAAAGTTATAAATAACAGTAGGAAAGAGAGA AGTAAATGAAAAGAGAAGATAAATGAATAAAATAAAAAGTTATAAATAACAGTAGGAAAGAGAGA A T TYW3 Ensembl:ENSG00000162623 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1442397590 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8049994 13465 RMVar_ID_13465 Human_SNP_ID_449400771 A-to-I Human chr10 - 120831484 120831484 120831484 AGGCTCACTGCAGGCTCTGCCTCCCGGGTTCAAGTGATTCTCCTACCTCAGCCTCCCGAGTAGCT AGGCTCACTGCAGGCTCTGCCTCCCGGGTTCAGGTGATTCTCCTACCTCAGCCTCCCGAGTAGCT T C WDR11-AS1 Ensembl:ENSG00000227165 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025430001 Functional Loss SNV dbSNP153 33..33 33 - - - 13466 RMVar_ID_13466 Human_SNP_ID_449664018 A-to-I Human chr10 - 121906877 121906877 121906877 TCCTTGGATTTTGGCCGGGCTCAGTGGCTCACACCTGTAATCCCACACTTTGGGAGGCCGAGACA TCCTTGGATTTTGGCCGGGCTCAGTGGCTCACGCCTGTAATCCCACACTTTGGGAGGCCGAGACA T C ATE1 Ensembl:ENSG00000107669 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1279544312 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8799,RMVar_hsa_circ_146819,RMVar_hsa_circ_278012,RMVar_hsa_circ_289965,RMVar_hsa_circ_309481,RMVar_hsa_circ_279098,RMVar_hsa_circ_146820,RMVar_hsa_circ_146830,RMVar_hsa_circ_274830,RMVar_hsa_circ_303726,RMVar_hsa_circ_146825,RMVar_hsa_circ_336451,RMVar_hsa_circ_146831,RMVar_hsa_circ_146832,RMVar_hsa_circ_67746,RMVar_hsa_circ_277276,RMVar_hsa_circ_18109,RMVar_hsa_circ_146838,RMVar_hsa_circ_146833,RMVar_hsa_circ_277003,RMVar_hsa_circ_377514,RMVar_hsa_circ_328240,RMVar_hsa_circ_14689,RMVar_hsa_circ_146836,RMVar_hsa_circ_146837,RMVar_hsa_circ_283069,RMVar_hsa_circ_280774,RMVar_hsa_circ_276906,RMVar_hsa_circ_146840,RMVar_hsa_circ_146841,RMVar_hsa_circ_146842,RMVar_hsa_circ_343199,RMVar_hsa_circ_146846,RMVar_hsa_circ_278987,RMVar_hsa_circ_146844,RMVar_hsa_circ_75179,RMVar_hsa_circ_300093,RMVar_hsa_circ_318347,RMVar_hsa_circ_297900,RMVar_hsa_circ_146848,RMVar_hsa_circ_146847,RMVar_hsa_circ_146845 13467 RMVar_ID_13467 Human_SNP_ID_449677317 A-to-I Human chr10 - 121958145 121958145 121958145 CAGTTCACTGTAATCTCTGCCTCCCCGGTTCAAGCAATTCTCCTGCTTCAGCCTCCTGAGTAGCT CAGTTCACTGTAATCTCTGCCTCCCCGGTTCAGGCAATTCTCCTGCTTCAGCCTCCTGAGTAGCT T C NSMCE4A Ensembl:ENSG00000107672 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs902758990 Functional Loss SNV dbSNP153 33..33 33 - - - 13468 RMVar_ID_13468 Human_SNP_ID_449677330 A-to-I Human chr10 - 121958197 121958197 121958197 GAGACAGAGTCTTGCTCTGTCACCCCCAGGCTAGAGTGCAGTGGCACGATCTCAGTTCACTGTAA GAGACAGAGTCTTGCTCTGTCACCCCCAGGCTGGAGTGCAGTGGCACGATCTCAGTTCACTGTAA T C NSMCE4A Ensembl:ENSG00000107672 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893768769 Functional Loss SNV dbSNP153 33..33 33 - - - 13469 RMVar_ID_13469 Human_SNP_ID_449678161 A-to-I Human chr10 - 121962024 121962024 121962024 CTCACTGCAACCTCCACCTCCTGGATTCAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGG CTCACTGCAACCTCCACCTCCTGGATTCAAGCCATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGG T G NSMCE4A Ensembl:ENSG00000107672 Protein coding intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1399618528 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1183418,Human_Splice_Rec_1183462 RMVar_hsa_circ_108707,RMVar_hsa_circ_320953,RMVar_hsa_circ_360202,RMVar_hsa_circ_146856,RMVar_hsa_circ_346425 13470 RMVar_ID_13470 Human_SNP_ID_449678163 A-to-I Human chr10 - 121962027 121962027 121962027 CAACTCACTGCAACCTCCACCTCCTGGATTCAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCT CAACTCACTGCAACCTCCACCTCCTGGATTCACGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCT T G NSMCE4A Ensembl:ENSG00000107672 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1312980692 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1183418,Human_Splice_Rec_1183462 RMVar_hsa_circ_108707,RMVar_hsa_circ_320953,RMVar_hsa_circ_360202,RMVar_hsa_circ_146856,RMVar_hsa_circ_346425 13471 RMVar_ID_13471 Human_SNP_ID_449678170 A-to-I Human chr10 - 121962041 121962041 121962041 CAGTGGCACCATCTCAACTCACTGCAACCTCCACCTCCTGGATTCAAGCAATTCTCCTGCCTCAG CAGTGGCACCATCTCAACTCACTGCAACCTCCCCCTCCTGGATTCAAGCAATTCTCCTGCCTCAG T G NSMCE4A Ensembl:ENSG00000107672 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1329880456 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1183418,Human_Splice_Rec_1183462 RMVar_hsa_circ_108707,RMVar_hsa_circ_320953,RMVar_hsa_circ_360202,RMVar_hsa_circ_146856,RMVar_hsa_circ_346425 13472 RMVar_ID_13472 Human_SNP_ID_449682055 A-to-I Human chr10 + 121976312 121976312 121976312 TTTTTAAGACCTTGCTCTGCCGAGGCTGGAGTACAGTGGCACTATCTTGGCTCACTGCAACCCCA TTTTTAAGACCTTGCTCTGCCGAGGCTGGAGTGCAGTGGCACTATCTTGGCTCACTGCAACCCCA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270409506 Functional Loss SNV dbSNP153 33..33 33 - - - 13473 RMVar_ID_13473 Human_SNP_ID_449682057 A-to-I Human chr10 + 121976320 121976320 121976320 ACCTTGCTCTGCCGAGGCTGGAGTACAGTGGCACTATCTTGGCTCACTGCAACCCCATCTCCTGA ACCTTGCTCTGCCGAGGCTGGAGTACAGTGGCCCTATCTTGGCTCACTGCAACCCCATCTCCTGA A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1225831516 Functional Loss SNV dbSNP153 33..33 33 - - - 13474 RMVar_ID_13474 Human_SNP_ID_449712539 A-to-I Human chr10 + 122090843 122090843 122090843 CAATCTCTGCTCAATGCAGCCTCGACCACCCCAGGATCCTCCCACTTCAGCCTCCCTAGTAGCTG CAATCTCTGCTCAATGCAGCCTCGACCACCCCGGGATCCTCCCACTTCAGCCTCCCTAGTAGCTG A G TACC2 Ensembl:ENSG00000138162 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1032515832 Functional Loss SNV dbSNP153 33..33 33 - - - 13475 RMVar_ID_13475 Human_SNP_ID_449712540 A-to-I Human chr10 + 122090843 122090843 122090843 CAATCTCTGCTCAATGCAGCCTCGACCACCCCAGGATCCTCCCACTTCAGCCTCCCTAGTAGCTG CAATCTCTGCTCAATGCAGCCTCGACCACCCCTGGATCCTCCCACTTCAGCCTCCCTAGTAGCTG A T TACC2 Ensembl:ENSG00000138162 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1032515832 Functional Loss SNV dbSNP153 33..33 33 - - - 13476 RMVar_ID_13476 Human_SNP_ID_449724608 A-to-I Human chr10 + 122136572 122136546 122136572 TGTGTGTATATATATATATATATATATATATTAGATGTAGTCTTGCTCTGTCGCCCAGGCTGGAG TGTGTGT__________________________GATGTAGTCTTGCTCTGTCGCCCAGGCTGGAG TATATATATATATATATATATATATTA T TACC2 Ensembl:ENSG00000138162 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1165052235 Functional Loss DEL dbSNP153 8..33 33 - - - RMVar_hsa_circ_146860,RMVar_hsa_circ_124449,RMVar_hsa_circ_301467 13477 RMVar_ID_13477 Human_SNP_ID_449746713 A-to-I Human chr10 + 122223226 122223226 122223226 CAGGTATGTGCCCGGCTAATTTTAGTATTTTTAGTAGAGATGGGGTTGGCCAGGTTGTTCTTGAA CAGGTATGTGCCCGGCTAATTTTAGTATTTTTGGTAGAGATGGGGTTGGCCAGGTTGTTCTTGAA A G TACC2 Ensembl:ENSG00000138162 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264878692 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17448,RMVar_hsa_circ_68929,RMVar_hsa_circ_75124,RMVar_hsa_circ_43383,RMVar_hsa_circ_26528 13478 RMVar_ID_13478 Human_SNP_ID_449786183 A-to-I Human chr10 + 122384691 122384691 122384691 AAATTGTTACTGCTCCAGGTGTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAATGC AAATTGTTACTGCTCCAGGTGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAATGC A G PLEKHA1 Ensembl:ENSG00000107679 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1362830563 Functional Loss SNV dbSNP153 33..33 33 - - - 13479 RMVar_ID_13479 Human_SNP_ID_449910306 A-to-I Human chr10 + 122893729 122893729 122893729 GGGAAGCTGAGGTGGGAGGATCACTTGAGCCCAAGAAGTCGAGGCTGTGGTGAGCTGAGATCGTA GGGAAGCTGAGGTGGGAGGATCACTTGAGCCCGAGAAGTCGAGGCTGTGGTGAGCTGAGATCGTA A G C10orf88B Ensembl:ENSG00000255624 Pseudogene intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1193496497 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79448,RMVar_hsa_circ_146902 13480 RMVar_ID_13480 Human_SNP_ID_449935579 A-to-I Human chr10 - 123001072 123001072 123001072 CTGGGAGGTGGAGCTTGCAGTGAGCCGAGATCACGGCACTGCACCCCAGCCTGGGCGACAGAGTG CTGGGAGGTGGAGCTTGCAGTGAGCCGAGATCGCGGCACTGCACCCCAGCCTGGGCGACAGAGTG T C IKZF5 Ensembl:ENSG00000095574 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1258835242 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24856379 RMVar_hsa_circ_330292,RMVar_hsa_circ_146907 13481 RMVar_ID_13481 Human_SNP_ID_449937926 A-to-I Human chr10 + 123010826 123010826 123010826 CTCTACCTCCAAGAAGTTTATCTTTTAGAGGAAAGGTTAGAACTATGTGCAACTAACCCCATGTC CTCTACCTCCAAGAAGTTTATCTTTTAGAGGAGAGGTTAGAACTATGTGCAACTAACCCCATGTC A G ACADSB Ensembl:ENSG00000196177 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1564744491 Functional Loss SNV dbSNP153 33..33 33 - - - 13482 RMVar_ID_13482 Human_SNP_ID_450200541 A-to-I Human chr10 - 124080853 124080853 124080853 GTCCATGGGAAAGAATGATTGGGCCGATGGACAGACAGATGGGTGAAAGGAAAACAGGCAAGAGT GTCCATGGGAAAGAATGATTGGGCCGATGGACGGACAGATGGGTGAAAGGAAAACAGGCAAGAGT T C CHST15 Ensembl:ENSG00000182022 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs944589586 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23441532 RMVar_hsa_circ_96525,RMVar_hsa_circ_146926 13483 RMVar_ID_13483 Human_SNP_ID_450280371 A-to-I Human chr10 - 124405558 124405558 124405558 TAATCACTGTTTGTTTCCCCTTTGTAGCTGGGAACTTCTGGGGTAGGACGTTGTCTGCTATCTCC TAATCACTGTTTGTTTCCCCTTTGTAGCTGGGGACTTCTGGGGTAGGACGTTGTCTGCTATCTCC T C OAT Ensembl:ENSG00000065154 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1171475806 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_861421,Human_RBP_ID_5942861,Human_RBP_ID_8758928,Human_RBP_ID_9254193,Human_RBP_ID_9343666,Human_RBP_ID_17772323,Human_RBP_ID_22431628,Human_RBP_ID_22568172,Human_RBP_ID_22639719,Human_RBP_ID_22752534 Human_Splice_Rec_1186316,Human_Splice_Rec_1186332,Human_Splice_Rec_1186354 RMVar_hsa_circ_61446,RMVar_hsa_circ_322913,RMVar_hsa_circ_325845,RMVar_hsa_circ_344537,RMVar_hsa_circ_351734,RMVar_hsa_circ_347649,RMVar_hsa_circ_146934 13484 RMVar_ID_13484 Human_SNP_ID_450296017 A-to-I Human chr10 + 124462413 124462413 124462413 GCTAGGGGGTTGGAGACCACCCTGGGCAACATAGGGAGACCCCGTCTCTGCCAAAAATTTAAAAA GCTAGGGGGTTGGAGACCACCCTGGGCAACATGGGGAGACCCCGTCTCTGCCAAAAATTTAAAAA A G LHPP Ensembl:ENSG00000107902 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1409527814 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102074,RMVar_hsa_circ_146937 13485 RMVar_ID_13485 Human_SNP_ID_450299282 A-to-I Human chr10 + 124472159 124472159 124472159 CATAGTGAAACCCCCGTCTTTACTAAATATACAAAAATCAGCTGGGTGTGGTGTTGTGCGCCTGT CATAGTGAAACCCCCGTCTTTACTAAATATACGAAAATCAGCTGGGTGTGGTGTTGTGCGCCTGT A G LHPP Ensembl:ENSG00000107902 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1227965119 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102074,RMVar_hsa_circ_146937 13486 RMVar_ID_13486 Human_SNP_ID_450299888 A-to-I Human chr10 + 124474281 124474281 124474281 TTCACCTCAGCCCCCAAAGTAGCTGAGACTACAAGTGCACACCACTGCACCTGGCCAATTTTTGT TTCACCTCAGCCCCCAAAGTAGCTGAGACTACGAGTGCACACCACTGCACCTGGCCAATTTTTGT A G LHPP Ensembl:ENSG00000107902 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1373194696 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102074,RMVar_hsa_circ_146937 13487 RMVar_ID_13487 Human_SNP_ID_450317938 A-to-I Human chr10 + 124538176 124538162 124538176 CATGCAGGGTCACCACGCGAGTCTCACCATGCAGGGTCACCATGCGGGGTCACCATGTGGGGTCA CATGCAGGGTCACCACGCG______________GGGTCACCATGCGGGGTCACCATGTGGGGTCA GAGTCTCACCATGCA G LHPP Ensembl:ENSG00000107902 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1564817480 Functional Loss DEL dbSNP153 20..33 33 - - - RMVar_hsa_circ_102074,RMVar_hsa_circ_146937,RMVar_hsa_circ_86169,RMVar_hsa_circ_113672,RMVar_hsa_circ_146946,RMVar_hsa_circ_146947 13488 RMVar_ID_13488 Human_SNP_ID_450317944 A-to-I Human chr10 + 124538176 124538176 124538176 CATGCAGGGTCACCACGCGAGTCTCACCATGCAGGGTCACCATGCGGGGTCACCATGTGGGGTCA CATGCAGGGTCACCACGCGAGTCTCACCATGCGGGGTCACCATGCGGGGTCACCATGTGGGGTCA A G LHPP Ensembl:ENSG00000107902 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs72837318 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102074,RMVar_hsa_circ_146937,RMVar_hsa_circ_86169,RMVar_hsa_circ_113672,RMVar_hsa_circ_146946,RMVar_hsa_circ_146947 13489 RMVar_ID_13489 Human_SNP_ID_450373376 A-to-I Human chr10 - 124750818 124750818 124750818 CCCAGCTATTTTTTGTAATTTTTGTAGAGACAAGGTTTCGCCATGTTACCCAGGCTGGACTCGAA CCCAGCTATTTTTTGTAATTTTTGTAGAGACAGGGTTTCGCCATGTTACCCAGGCTGGACTCGAA T C AC068896.3,EEF1AKMT2 Ensembl:ENSG00000258539,Ensembl:ENSG00000203791 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs901611145 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_333711,RMVar_hsa_circ_96352,RMVar_hsa_circ_127559,RMVar_hsa_circ_113129,RMVar_hsa_circ_146961,RMVar_hsa_circ_66558,RMVar_hsa_circ_94477,RMVar_hsa_circ_146966,RMVar_hsa_circ_146967,RMVar_hsa_circ_146968 13490 RMVar_ID_13490 Human_SNP_ID_450373393 A-to-I Human chr10 - 124750891 124750891 124750891 AACCTCCTGGGCTCAAGTGATCCTCCAACCTCAGCCTCCATAGTAGGTGGGACCACAGGCACGTG AACCTCCTGGGCTCAAGTGATCCTCCAACCTCCGCCTCCATAGTAGGTGGGACCACAGGCACGTG T G AC068896.3,EEF1AKMT2 Ensembl:ENSG00000258539,Ensembl:ENSG00000203791 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1341828913 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_333711,RMVar_hsa_circ_96352,RMVar_hsa_circ_127559,RMVar_hsa_circ_113129,RMVar_hsa_circ_146961,RMVar_hsa_circ_66558,RMVar_hsa_circ_94477,RMVar_hsa_circ_146966,RMVar_hsa_circ_146967,RMVar_hsa_circ_146968 13491 RMVar_ID_13491 Human_SNP_ID_450373993 A-to-I Human chr10 - 124753003 124753003 124753003 TTAAGTGATCCTCCTGTCTCAGCCTCCCTAGCAGCTGGGGCTACAGGTGCATGCCACCATGTCAG TTAAGTGATCCTCCTGTCTCAGCCTCCCTAGCGGCTGGGGCTACAGGTGCATGCCACCATGTCAG T C AC068896.3,EEF1AKMT2 Ensembl:ENSG00000258539,Ensembl:ENSG00000203791 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1564896286 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_333711,RMVar_hsa_circ_96352,RMVar_hsa_circ_127559,RMVar_hsa_circ_113129,RMVar_hsa_circ_146961,RMVar_hsa_circ_66558,RMVar_hsa_circ_94477,RMVar_hsa_circ_146966,RMVar_hsa_circ_146967,RMVar_hsa_circ_146968 13492 RMVar_ID_13492 Human_SNP_ID_450374076 A-to-I Human chr10 - 124753307 124753307 124753307 TCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCGCCTGCCACCACCCCTG TCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTGGCTGGGACTACAGGCGCCTGCCACCACCCCTG T C AC068896.3,EEF1AKMT2 Ensembl:ENSG00000258539,Ensembl:ENSG00000203791 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs896743855 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_333711,RMVar_hsa_circ_96352,RMVar_hsa_circ_127559,RMVar_hsa_circ_113129,RMVar_hsa_circ_146961,RMVar_hsa_circ_66558,RMVar_hsa_circ_94477,RMVar_hsa_circ_146966,RMVar_hsa_circ_146967,RMVar_hsa_circ_146968 13493 RMVar_ID_13493 Human_SNP_ID_450376083 A-to-I Human chr10 - 124762367 124762357 124762368 TTGTCCAGGCTGGTCTGGAACTCCTGGGCTCAAGTGATTCTCCCACCTGGCCTCCCAAAGTGCTG TTGTCCAGGCTGGTCTGGAACTCCTGGGCTC___________CCACCTGGCCTCCCAAAGTGCTG GGAGAATCACTT G AC068896.3,EEF1AKMT2 Ensembl:ENSG00000258539,Ensembl:ENSG00000203791 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1438338048 Functional Loss DEL dbSNP153 32..42 33 - - - Human_Splice_Rec_1186511,Human_Splice_Rec_1186523,Human_Splice_Rec_1186539 RMVar_hsa_circ_333711,RMVar_hsa_circ_96352,RMVar_hsa_circ_113129,RMVar_hsa_circ_66558,RMVar_hsa_circ_94477,RMVar_hsa_circ_146966,RMVar_hsa_circ_146967,RMVar_hsa_circ_146968,RMVar_hsa_circ_146971,RMVar_hsa_circ_146970,RMVar_hsa_circ_278620,RMVar_hsa_circ_360501,RMVar_hsa_circ_146969,RMVar_hsa_circ_355304,RMVar_hsa_circ_277321,RMVar_hsa_circ_89000 13494 RMVar_ID_13494 Human_SNP_ID_450376155 A-to-I Human chr10 - 124762550 124762550 124762550 TCTGTCTCTCTCTCTGTTGCCCAGGTTGGAGTACAGTGGCAGGATTTTGGCTCACTGCAGCCTTG TCTGTCTCTCTCTCTGTTGCCCAGGTTGGAGTGCAGTGGCAGGATTTTGGCTCACTGCAGCCTTG T C AC068896.3,EEF1AKMT2 Ensembl:ENSG00000258539,Ensembl:ENSG00000203791 Protein coding,Protein coding intron,intron GSE38233;GSE112787 cultured B-cells;293 Flip-In T-REx cells,empty vector - 24183664,29967493 RNA-Seq:(High) rs1256700169 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1186510,Human_Splice_Rec_1186522,Human_Splice_Rec_1186538 RMVar_hsa_circ_333711,RMVar_hsa_circ_96352,RMVar_hsa_circ_113129,RMVar_hsa_circ_66558,RMVar_hsa_circ_94477,RMVar_hsa_circ_146966,RMVar_hsa_circ_146967,RMVar_hsa_circ_146968,RMVar_hsa_circ_146971,RMVar_hsa_circ_146970,RMVar_hsa_circ_278620,RMVar_hsa_circ_360501,RMVar_hsa_circ_146969,RMVar_hsa_circ_355304,RMVar_hsa_circ_277321,RMVar_hsa_circ_89000 13495 RMVar_ID_13495 Human_SNP_ID_450378436 A-to-I Human chr10 - 124771276 124771275 124771276 GCTAACATGGTGAAACCCCATCTCTACTAAAAATACAAAGAATTAGCCAGGTGTGGTGGCAGGTG GCTAACATGGTGAAACCCCATCTCTACTAAAA_TACAAAGAATTAGCCAGGTGTGGTGGCAGGTG AT A AC068896.3,EEF1AKMT2 Ensembl:ENSG00000258539,Ensembl:ENSG00000203791 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1363106335 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_333711,RMVar_hsa_circ_96352,RMVar_hsa_circ_113129,RMVar_hsa_circ_66558,RMVar_hsa_circ_146967,RMVar_hsa_circ_146968,RMVar_hsa_circ_146971,RMVar_hsa_circ_146970,RMVar_hsa_circ_278620,RMVar_hsa_circ_146969,RMVar_hsa_circ_355304,RMVar_hsa_circ_277321,RMVar_hsa_circ_89000,RMVar_hsa_circ_58897,RMVar_hsa_circ_341144 13496 RMVar_ID_13496 Human_SNP_ID_450378438 A-to-I Human chr10 - 124771276 124771276 124771276 GCTAACATGGTGAAACCCCATCTCTACTAAAAATACAAAGAATTAGCCAGGTGTGGTGGCAGGTG GCTAACATGGTGAAACCCCATCTCTACTAAAACTACAAAGAATTAGCCAGGTGTGGTGGCAGGTG T G AC068896.3,EEF1AKMT2 Ensembl:ENSG00000258539,Ensembl:ENSG00000203791 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs545690458 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_333711,RMVar_hsa_circ_96352,RMVar_hsa_circ_113129,RMVar_hsa_circ_66558,RMVar_hsa_circ_146967,RMVar_hsa_circ_146968,RMVar_hsa_circ_146971,RMVar_hsa_circ_146970,RMVar_hsa_circ_278620,RMVar_hsa_circ_146969,RMVar_hsa_circ_355304,RMVar_hsa_circ_277321,RMVar_hsa_circ_89000,RMVar_hsa_circ_58897,RMVar_hsa_circ_341144 13497 RMVar_ID_13497 Human_SNP_ID_450379067 A-to-I Human chr10 - 124773392 124773392 124773392 CCATATCTCCACCAAAAGTACAAAAAATAGCCAGGTGTGGTGGCGGGCACCTGTAGTCCCAACTA CCATATCTCCACCAAAAGTACAAAAAATAGCCGGGTGTGGTGGCGGGCACCTGTAGTCCCAACTA T C AC068896.3,EEF1AKMT2 Ensembl:ENSG00000258539,Ensembl:ENSG00000203791 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1142693 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_333711,RMVar_hsa_circ_96352,RMVar_hsa_circ_113129,RMVar_hsa_circ_66558,RMVar_hsa_circ_146967,RMVar_hsa_circ_146968,RMVar_hsa_circ_146971,RMVar_hsa_circ_146970,RMVar_hsa_circ_278620,RMVar_hsa_circ_146969,RMVar_hsa_circ_355304,RMVar_hsa_circ_277321,RMVar_hsa_circ_89000,RMVar_hsa_circ_58897,RMVar_hsa_circ_341144 13498 RMVar_ID_13498 Human_SNP_ID_450379074 A-to-I Human chr10 - 124773436 124773428 124773437 TTTGAGGTCAGGAGTTTGGGACTAGCCTGGCCAGCATGGTGAAACCATATCTCCACCAAAAGTAC TTTGAGGTCAGGAGTTTGGGACTAGCCTGGC_________GAAACCATATCTCCACCAAAAGTAC CACCATGCTG C AC068896.3,EEF1AKMT2 Ensembl:ENSG00000258539,Ensembl:ENSG00000203791 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1407519410 Functional Loss DEL dbSNP153 32..40 33 - - - RMVar_hsa_circ_333711,RMVar_hsa_circ_96352,RMVar_hsa_circ_113129,RMVar_hsa_circ_66558,RMVar_hsa_circ_146967,RMVar_hsa_circ_146968,RMVar_hsa_circ_146971,RMVar_hsa_circ_146970,RMVar_hsa_circ_278620,RMVar_hsa_circ_146969,RMVar_hsa_circ_355304,RMVar_hsa_circ_277321,RMVar_hsa_circ_89000,RMVar_hsa_circ_58897,RMVar_hsa_circ_341144 13499 RMVar_ID_13499 Human_SNP_ID_450379078 A-to-I Human chr10 - 124773436 124773436 124773436 TTTGAGGTCAGGAGTTTGGGACTAGCCTGGCCAGCATGGTGAAACCATATCTCCACCAAAAGTAC TTTGAGGTCAGGAGTTTGGGACTAGCCTGGCCGGCATGGTGAAACCATATCTCCACCAAAAGTAC T C AC068896.3,EEF1AKMT2 Ensembl:ENSG00000258539,Ensembl:ENSG00000203791 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1466233384 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_333711,RMVar_hsa_circ_96352,RMVar_hsa_circ_113129,RMVar_hsa_circ_66558,RMVar_hsa_circ_146967,RMVar_hsa_circ_146968,RMVar_hsa_circ_146971,RMVar_hsa_circ_146970,RMVar_hsa_circ_278620,RMVar_hsa_circ_146969,RMVar_hsa_circ_355304,RMVar_hsa_circ_277321,RMVar_hsa_circ_89000,RMVar_hsa_circ_58897,RMVar_hsa_circ_341144 13500 RMVar_ID_13500 Human_SNP_ID_450379102 A-to-I Human chr10 - 124773522 124773522 124773522 GCCAATTAAAAACCTTACAGTGGGACAGGCGCAGTGGCTAATGCCTGTAATCCCAACACTTTAGG GCCAATTAAAAACCTTACAGTGGGACAGGCGCGGTGGCTAATGCCTGTAATCCCAACACTTTAGG T C AC068896.3,EEF1AKMT2 Ensembl:ENSG00000258539,Ensembl:ENSG00000203791 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1033066471 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_333711,RMVar_hsa_circ_96352,RMVar_hsa_circ_113129,RMVar_hsa_circ_66558,RMVar_hsa_circ_146967,RMVar_hsa_circ_146968,RMVar_hsa_circ_146971,RMVar_hsa_circ_146970,RMVar_hsa_circ_278620,RMVar_hsa_circ_146969,RMVar_hsa_circ_355304,RMVar_hsa_circ_277321,RMVar_hsa_circ_89000,RMVar_hsa_circ_58897,RMVar_hsa_circ_341144 13501 RMVar_ID_13501 Human_SNP_ID_450380080 A-to-I Human chr10 - 124777029 124777029 124777029 GTGATCCACCTGCCTTGGCCTCCCAAAATGATAGGATTACAAGCTTGAGCCACCATGCCCGGCCC GTGATCCACCTGCCTTGGCCTCCCAAAATGATGGGATTACAAGCTTGAGCCACCATGCCCGGCCC T C AC068896.3,EEF1AKMT2 Ensembl:ENSG00000258539,Ensembl:ENSG00000203791 Protein coding,Protein coding intron,intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1343705491 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5943688,Human_RBP_ID_11299783,Human_RBP_ID_24856489 RMVar_hsa_circ_96352,RMVar_hsa_circ_113129,RMVar_hsa_circ_146967,RMVar_hsa_circ_146968,RMVar_hsa_circ_146971,RMVar_hsa_circ_355304,RMVar_hsa_circ_277321,RMVar_hsa_circ_89000,RMVar_hsa_circ_58897,RMVar_hsa_circ_146973,RMVar_hsa_circ_317308 13502 RMVar_ID_13502 Human_SNP_ID_450380123 A-to-I Human chr10 - 124777240 124777240 124777240 AGTTTTGCTCTTGTAGCCCAGGCTGGAGTGCAATGGCGCGATCTTGGCTCACTATAACCTCCACC AGTTTTGCTCTTGTAGCCCAGGCTGGAGTGCAGTGGCGCGATCTTGGCTCACTATAACCTCCACC T C AC068896.3,EEF1AKMT2 Ensembl:ENSG00000258539,Ensembl:ENSG00000203791 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1402635854 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11299794 RMVar_hsa_circ_96352,RMVar_hsa_circ_113129,RMVar_hsa_circ_146967,RMVar_hsa_circ_146968,RMVar_hsa_circ_146971,RMVar_hsa_circ_355304,RMVar_hsa_circ_277321,RMVar_hsa_circ_89000,RMVar_hsa_circ_58897,RMVar_hsa_circ_146973,RMVar_hsa_circ_317308 13503 RMVar_ID_13503 Human_SNP_ID_450380133 A-to-I Human chr10 - 124777272 124777270 124777272 TTTTTTTCTTTTTTTTTTTTTTTTTGAGTCAGAGTTTTGCTCTTGTAGCCCAGGCTGGAGTGCAA TTTTTTTCTTTTTTTTTTTTTTTTTGAGTCAG__TTTTGCTCTTGTAGCCCAGGCTGGAGTGCAA ACT A AC068896.3,EEF1AKMT2 Ensembl:ENSG00000258539,Ensembl:ENSG00000203791 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs758534225 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_11299795,Human_RBP_ID_23441920 RMVar_hsa_circ_96352,RMVar_hsa_circ_113129,RMVar_hsa_circ_146967,RMVar_hsa_circ_146968,RMVar_hsa_circ_146971,RMVar_hsa_circ_355304,RMVar_hsa_circ_277321,RMVar_hsa_circ_89000,RMVar_hsa_circ_58897,RMVar_hsa_circ_146973,RMVar_hsa_circ_317308 13504 RMVar_ID_13504 Human_SNP_ID_450380135 A-to-I Human chr10 - 124777272 124777272 124777272 TTTTTTTCTTTTTTTTTTTTTTTTTGAGTCAGAGTTTTGCTCTTGTAGCCCAGGCTGGAGTGCAA TTTTTTTCTTTTTTTTTTTTTTTTTGAGTCAGTGTTTTGCTCTTGTAGCCCAGGCTGGAGTGCAA T A AC068896.3,EEF1AKMT2 Ensembl:ENSG00000258539,Ensembl:ENSG00000203791 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1379589613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11299795,Human_RBP_ID_23441920 RMVar_hsa_circ_96352,RMVar_hsa_circ_113129,RMVar_hsa_circ_146967,RMVar_hsa_circ_146968,RMVar_hsa_circ_146971,RMVar_hsa_circ_355304,RMVar_hsa_circ_277321,RMVar_hsa_circ_89000,RMVar_hsa_circ_58897,RMVar_hsa_circ_146973,RMVar_hsa_circ_317308 13505 RMVar_ID_13505 Human_SNP_ID_450380277 A-to-I Human chr10 - 124777692 124777689 124777692 CCTGTCTCTACAAAAAAAAACAAAAAACAAAAAAACAAAAATTAACCAGGCATGGTGGTGGCATG CCTGTCTCTACAAAAAAAAACAAAAAACAAAA___CAAAAATTAACCAGGCATGGTGGTGGCATG GTTT G AC068896.3,EEF1AKMT2 Ensembl:ENSG00000258539,Ensembl:ENSG00000203791 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1331540291 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_8244537,Human_RBP_ID_9580561,Human_RBP_ID_24856492 RMVar_hsa_circ_96352,RMVar_hsa_circ_113129,RMVar_hsa_circ_146967,RMVar_hsa_circ_146968,RMVar_hsa_circ_146971,RMVar_hsa_circ_355304,RMVar_hsa_circ_277321,RMVar_hsa_circ_89000,RMVar_hsa_circ_58897,RMVar_hsa_circ_146973,RMVar_hsa_circ_317308 13506 RMVar_ID_13506 Human_SNP_ID_450380386 A-to-I Human chr10 - 124778091 124778091 124778091 CAACTCCTGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCACCCG CAACTCCTGGGTTCAAGCGATTCTCCTGCCTCTGCCTCCCAAGTAGCTGGGATTACAGGCACCCG T A AC068896.3,EEF1AKMT2 Ensembl:ENSG00000258539,Ensembl:ENSG00000203791 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1453131707 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96352,RMVar_hsa_circ_113129,RMVar_hsa_circ_146967,RMVar_hsa_circ_146968,RMVar_hsa_circ_146971,RMVar_hsa_circ_355304,RMVar_hsa_circ_277321,RMVar_hsa_circ_89000,RMVar_hsa_circ_58897,RMVar_hsa_circ_146973,RMVar_hsa_circ_317308 13507 RMVar_ID_13507 Human_SNP_ID_450380681 A-to-I Human chr10 - 124779163 124779163 124779163 TCACGCTGTTGCATTCCAGTCTGGGTGACAGAAGGAAACCCTGTTTCCATAAAAAAAAGAAAAAG TCACGCTGTTGCATTCCAGTCTGGGTGACAGAGGGAAACCCTGTTTCCATAAAAAAAAGAAAAAG T C AC068896.3,EEF1AKMT2 Ensembl:ENSG00000258539,Ensembl:ENSG00000203791 Protein coding,Protein coding intron,intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1439416441 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_373276 RMVar_hsa_circ_96352,RMVar_hsa_circ_113129,RMVar_hsa_circ_146967,RMVar_hsa_circ_146968,RMVar_hsa_circ_146971,RMVar_hsa_circ_355304,RMVar_hsa_circ_277321,RMVar_hsa_circ_89000,RMVar_hsa_circ_58897,RMVar_hsa_circ_146973,RMVar_hsa_circ_317308 13508 RMVar_ID_13508 Human_SNP_ID_450380959 A-to-I Human chr10 - 124779941 124779941 124779941 CTTTTGCCTCAGCCTCCCGAGTAGCTGGGACTACATGTGCCCGCCACCACGCCTGGCTAATTTTT CTTTTGCCTCAGCCTCCCGAGTAGCTGGGACTGCATGTGCCCGCCACCACGCCTGGCTAATTTTT T C AC068896.3,EEF1AKMT2 Ensembl:ENSG00000258539,Ensembl:ENSG00000203791 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1202499016 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96352,RMVar_hsa_circ_113129,RMVar_hsa_circ_146967,RMVar_hsa_circ_146968,RMVar_hsa_circ_146971,RMVar_hsa_circ_355304,RMVar_hsa_circ_277321,RMVar_hsa_circ_89000,RMVar_hsa_circ_58897,RMVar_hsa_circ_146973,RMVar_hsa_circ_317308 13509 RMVar_ID_13509 Human_SNP_ID_450380984 A-to-I Human chr10 - 124780065 124780063 124780065 TTTATTCTGTTTCTTTTTGTTTTTTGAGACAGAGTCTTGCTCTGTCGCCCAGGCTGGAGTGCTGG TTTATTCTGTTTCTTTTTGTTTTTTGAGACAG__TCTTGCTCTGTCGCCCAGGCTGGAGTGCTGG ACT A AC068896.3,EEF1AKMT2 Ensembl:ENSG00000258539,Ensembl:ENSG00000203791 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs757697358 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_11299892,Human_RBP_ID_23441948 RMVar_hsa_circ_96352,RMVar_hsa_circ_113129,RMVar_hsa_circ_146967,RMVar_hsa_circ_146968,RMVar_hsa_circ_146971,RMVar_hsa_circ_355304,RMVar_hsa_circ_277321,RMVar_hsa_circ_89000,RMVar_hsa_circ_58897,RMVar_hsa_circ_146973,RMVar_hsa_circ_317308 13510 RMVar_ID_13510 Human_SNP_ID_450380985 A-to-I Human chr10 - 124780067 124780067 124780067 TATTTATTCTGTTTCTTTTTGTTTTTTGAGACAGAGTCTTGCTCTGTCGCCCAGGCTGGAGTGCT TATTTATTCTGTTTCTTTTTGTTTTTTGAGACGGAGTCTTGCTCTGTCGCCCAGGCTGGAGTGCT T C AC068896.3,EEF1AKMT2 Ensembl:ENSG00000258539,Ensembl:ENSG00000203791 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054153858 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11299892 RMVar_hsa_circ_96352,RMVar_hsa_circ_113129,RMVar_hsa_circ_146967,RMVar_hsa_circ_146968,RMVar_hsa_circ_146971,RMVar_hsa_circ_355304,RMVar_hsa_circ_277321,RMVar_hsa_circ_89000,RMVar_hsa_circ_58897,RMVar_hsa_circ_146973,RMVar_hsa_circ_317308 13511 RMVar_ID_13511 Human_SNP_ID_450381234 A-to-I Human chr10 - 124781070 124781070 124781070 GTGGTGGCATGCCCTTGTAGTCCCAGCTACTCAGGAGACTGAGGCAGGGGAATAGCTTGAACCCG GTGGTGGCATGCCCTTGTAGTCCCAGCTACTCGGGAGACTGAGGCAGGGGAATAGCTTGAACCCG T C AC068896.3,EEF1AKMT2 Ensembl:ENSG00000258539,Ensembl:ENSG00000203791 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1012461208 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96352,RMVar_hsa_circ_113129,RMVar_hsa_circ_146967,RMVar_hsa_circ_146968,RMVar_hsa_circ_146971,RMVar_hsa_circ_355304,RMVar_hsa_circ_277321,RMVar_hsa_circ_89000,RMVar_hsa_circ_58897,RMVar_hsa_circ_146973,RMVar_hsa_circ_317308 13512 RMVar_ID_13512 Human_SNP_ID_450381235 A-to-I Human chr10 - 124781074 124781074 124781074 GGGCGTGGTGGCATGCCCTTGTAGTCCCAGCTACTCAGGAGACTGAGGCAGGGGAATAGCTTGAA GGGCGTGGTGGCATGCCCTTGTAGTCCCAGCTCCTCAGGAGACTGAGGCAGGGGAATAGCTTGAA T G AC068896.3,EEF1AKMT2 Ensembl:ENSG00000258539,Ensembl:ENSG00000203791 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs534405600 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96352,RMVar_hsa_circ_113129,RMVar_hsa_circ_146967,RMVar_hsa_circ_146968,RMVar_hsa_circ_146971,RMVar_hsa_circ_355304,RMVar_hsa_circ_277321,RMVar_hsa_circ_89000,RMVar_hsa_circ_58897,RMVar_hsa_circ_146973,RMVar_hsa_circ_317308 13513 RMVar_ID_13513 Human_SNP_ID_450381334 A-to-I Human chr10 - 124781416 124781416 124781416 CACCACCACACCCGGCTACTTTTTGTGTTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCGGGC CACCACCACACCCGGCTACTTTTTGTGTTTTTGGTAGAGATGGGGTTTCACCATGTTGGCCGGGC T C AC068896.3,EEF1AKMT2 Ensembl:ENSG00000258539,Ensembl:ENSG00000203791 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1026847265 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96352,RMVar_hsa_circ_113129,RMVar_hsa_circ_146967,RMVar_hsa_circ_146968,RMVar_hsa_circ_146971,RMVar_hsa_circ_355304,RMVar_hsa_circ_277321,RMVar_hsa_circ_89000,RMVar_hsa_circ_58897,RMVar_hsa_circ_146973,RMVar_hsa_circ_317308 13514 RMVar_ID_13514 Human_SNP_ID_450381571 A-to-I Human chr10 - 124782326 124782326 124782326 CTCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCACCCGGCCGGTCTTG CTCCCGCCTCGGCCTCCCAAAGTGCTGGGATTTCAGGCGTGAGCCACCGCACCCGGCCGGTCTTG T A AC068896.3,EEF1AKMT2 Ensembl:ENSG00000258539,Ensembl:ENSG00000203791 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs955196579 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22568187,Human_RBP_ID_24792091 RMVar_hsa_circ_96352,RMVar_hsa_circ_113129,RMVar_hsa_circ_146967,RMVar_hsa_circ_146968,RMVar_hsa_circ_146971,RMVar_hsa_circ_355304,RMVar_hsa_circ_277321,RMVar_hsa_circ_89000,RMVar_hsa_circ_58897,RMVar_hsa_circ_146973,RMVar_hsa_circ_317308 13515 RMVar_ID_13515 Human_SNP_ID_450381572 A-to-I Human chr10 - 124782326 124782326 124782326 CTCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCACCCGGCCGGTCTTG CTCCCGCCTCGGCCTCCCAAAGTGCTGGGATTCCAGGCGTGAGCCACCGCACCCGGCCGGTCTTG T G AC068896.3,EEF1AKMT2 Ensembl:ENSG00000258539,Ensembl:ENSG00000203791 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs955196579 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22568187,Human_RBP_ID_24792091 RMVar_hsa_circ_96352,RMVar_hsa_circ_113129,RMVar_hsa_circ_146967,RMVar_hsa_circ_146968,RMVar_hsa_circ_146971,RMVar_hsa_circ_355304,RMVar_hsa_circ_277321,RMVar_hsa_circ_89000,RMVar_hsa_circ_58897,RMVar_hsa_circ_146973,RMVar_hsa_circ_317308 13516 RMVar_ID_13516 Human_SNP_ID_450381980 A-to-I Human chr10 - 124783395 124783395 124783395 TTATGCCGGCAATCCTAGCACTCTGGGAGGCCAAGGCCGGTGGATCACTTGAGGTCAGCAGTTTG TTATGCCGGCAATCCTAGCACTCTGGGAGGCCGAGGCCGGTGGATCACTTGAGGTCAGCAGTTTG T C AC068896.3,EEF1AKMT2 Ensembl:ENSG00000258539,Ensembl:ENSG00000203791 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1328965138 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11300034,Human_RBP_ID_19484921,Human_RBP_ID_22787826 Human_miRNA_ID_2217864 RMVar_hsa_circ_96352,RMVar_hsa_circ_113129,RMVar_hsa_circ_146967,RMVar_hsa_circ_146968,RMVar_hsa_circ_146971,RMVar_hsa_circ_355304,RMVar_hsa_circ_277321,RMVar_hsa_circ_89000,RMVar_hsa_circ_58897,RMVar_hsa_circ_146973,RMVar_hsa_circ_317308 13517 RMVar_ID_13517 Human_SNP_ID_450382077 A-to-I Human chr10 - 124783784 124783784 124783784 AGCCAGGTTTGGTTGGTGGCAAGTGCACCTGTAGTCCCAGCTACTTGGGAGGCTGAAGTGGGAGG AGCCAGGTTTGGTTGGTGGCAAGTGCACCTGTCGTCCCAGCTACTTGGGAGGCTGAAGTGGGAGG T G AC068896.3,EEF1AKMT2 Ensembl:ENSG00000258539,Ensembl:ENSG00000203791 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1196077087 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23151723 RMVar_hsa_circ_96352,RMVar_hsa_circ_113129,RMVar_hsa_circ_146967,RMVar_hsa_circ_146968,RMVar_hsa_circ_146971,RMVar_hsa_circ_355304,RMVar_hsa_circ_277321,RMVar_hsa_circ_89000,RMVar_hsa_circ_58897,RMVar_hsa_circ_146973,RMVar_hsa_circ_317308 13518 RMVar_ID_13518 Human_SNP_ID_450382135 A-to-I Human chr10 - 124784003 124784003 124784003 CCTGACCAACATGGAGAAACCTTGTCTCTACTAAAAATATAAAATTGGTTGGGCGTGGTGGTGCA CCTGACCAACATGGAGAAACCTTGTCTCTACTGAAAATATAAAATTGGTTGGGCGTGGTGGTGCA T C AC068896.3,EEF1AKMT2 Ensembl:ENSG00000258539,Ensembl:ENSG00000203791 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs559612729 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11300055,Human_RBP_ID_17772436,Human_RBP_ID_22878864,Human_RBP_ID_24792122 RMVar_hsa_circ_96352,RMVar_hsa_circ_113129,RMVar_hsa_circ_146967,RMVar_hsa_circ_146968,RMVar_hsa_circ_146971,RMVar_hsa_circ_355304,RMVar_hsa_circ_277321,RMVar_hsa_circ_89000,RMVar_hsa_circ_58897,RMVar_hsa_circ_146973,RMVar_hsa_circ_317308 13519 RMVar_ID_13519 Human_SNP_ID_450382596 A-to-I Human chr10 - 124785774 124785774 124785774 CTCCTGCCTCAGCCTCCTGAGTAGATGGGATTACAGGTGCGCGCCAGCACGCCTGGCTAATTTTT CTCCTGCCTCAGCCTCCTGAGTAGATGGGATTCCAGGTGCGCGCCAGCACGCCTGGCTAATTTTT T G AC068896.3,EEF1AKMT2 Ensembl:ENSG00000258539,Ensembl:ENSG00000203791 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1037337404 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96352,RMVar_hsa_circ_113129,RMVar_hsa_circ_146967,RMVar_hsa_circ_146968,RMVar_hsa_circ_146971,RMVar_hsa_circ_355304,RMVar_hsa_circ_277321,RMVar_hsa_circ_89000,RMVar_hsa_circ_58897,RMVar_hsa_circ_146973,RMVar_hsa_circ_317308 13520 RMVar_ID_13520 Human_SNP_ID_450382598 A-to-I Human chr10 - 124785784 124785784 124785784 TCAAGTGATTCTCCTGCCTCAGCCTCCTGAGTAGATGGGATTACAGGTGCGCGCCAGCACGCCTG TCAAGTGATTCTCCTGCCTCAGCCTCCTGAGTGGATGGGATTACAGGTGCGCGCCAGCACGCCTG T C AC068896.3,EEF1AKMT2 Ensembl:ENSG00000258539,Ensembl:ENSG00000203791 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs778601613 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96352,RMVar_hsa_circ_113129,RMVar_hsa_circ_146967,RMVar_hsa_circ_146968,RMVar_hsa_circ_146971,RMVar_hsa_circ_355304,RMVar_hsa_circ_277321,RMVar_hsa_circ_89000,RMVar_hsa_circ_58897,RMVar_hsa_circ_146973,RMVar_hsa_circ_317308 13521 RMVar_ID_13521 Human_SNP_ID_450382608 A-to-I Human chr10 - 124785814 124785814 124785814 TCGGCTCACTGCAACCTCCACCTGCAGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCTGAGTAGA TCGGCTCACTGCAACCTCCACCTGCAGGGTTCCAGTGATTCTCCTGCCTCAGCCTCCTGAGTAGA T G AC068896.3,EEF1AKMT2 Ensembl:ENSG00000258539,Ensembl:ENSG00000203791 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1238360252 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96352,RMVar_hsa_circ_113129,RMVar_hsa_circ_146967,RMVar_hsa_circ_146968,RMVar_hsa_circ_146971,RMVar_hsa_circ_355304,RMVar_hsa_circ_277321,RMVar_hsa_circ_89000,RMVar_hsa_circ_58897,RMVar_hsa_circ_146973,RMVar_hsa_circ_317308 13522 RMVar_ID_13522 Human_SNP_ID_450382878 A-to-I Human chr10 - 124786694 124786694 124786694 GCGATTTTCCTGCCTCAGCCTCCTGAGTAGCTAGGATTACAGGCGTACACCATGCCTGGTTAATT GCGATTTTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCGTACACCATGCCTGGTTAATT T C AC068896.3,EEF1AKMT2 Ensembl:ENSG00000258539,Ensembl:ENSG00000203791 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1189182194 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96352,RMVar_hsa_circ_113129,RMVar_hsa_circ_146967,RMVar_hsa_circ_146968,RMVar_hsa_circ_146971,RMVar_hsa_circ_355304,RMVar_hsa_circ_277321,RMVar_hsa_circ_89000,RMVar_hsa_circ_58897,RMVar_hsa_circ_146973,RMVar_hsa_circ_317308 13523 RMVar_ID_13523 Human_SNP_ID_450382892 A-to-I Human chr10 - 124786727 124786727 124786727 CAGCTCACTGCAGCCTCTGCTTCCTGGGTTCAAGCGATTTTCCTGCCTCAGCCTCCTGAGTAGCT CAGCTCACTGCAGCCTCTGCTTCCTGGGTTCACGCGATTTTCCTGCCTCAGCCTCCTGAGTAGCT T G AC068896.3,EEF1AKMT2 Ensembl:ENSG00000258539,Ensembl:ENSG00000203791 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1554920211 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96352,RMVar_hsa_circ_113129,RMVar_hsa_circ_146967,RMVar_hsa_circ_146968,RMVar_hsa_circ_146971,RMVar_hsa_circ_355304,RMVar_hsa_circ_277321,RMVar_hsa_circ_89000,RMVar_hsa_circ_58897,RMVar_hsa_circ_146973,RMVar_hsa_circ_317308 13524 RMVar_ID_13524 Human_SNP_ID_450383094 A-to-I Human chr10 - 124787350 124787350 124787350 TGGCTCACTGCAACCTTCACCACCTGGGTTCAAGTGGTTCTCGTGCCTCAGCCTCATGAGTAGCT TGGCTCACTGCAACCTTCACCACCTGGGTTCAGGTGGTTCTCGTGCCTCAGCCTCATGAGTAGCT T C AC068896.3,EEF1AKMT2 Ensembl:ENSG00000258539,Ensembl:ENSG00000203791 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1282879274 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11300198 RMVar_hsa_circ_96352,RMVar_hsa_circ_113129,RMVar_hsa_circ_146967,RMVar_hsa_circ_146968,RMVar_hsa_circ_146971,RMVar_hsa_circ_355304,RMVar_hsa_circ_277321,RMVar_hsa_circ_89000,RMVar_hsa_circ_58897,RMVar_hsa_circ_146973,RMVar_hsa_circ_317308 13525 RMVar_ID_13525 Human_SNP_ID_450383200 A-to-I Human chr10 - 124787678 124787678 124787678 GCACTGGTGAGATCATGGCACATTGTAGCCTCAACCTCTCAGGCTCAAGCGATCCTGTCGCCTCA GCACTGGTGAGATCATGGCACATTGTAGCCTCCACCTCTCAGGCTCAAGCGATCCTGTCGCCTCA T G AC068896.3,EEF1AKMT2 Ensembl:ENSG00000258539,Ensembl:ENSG00000203791 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs552844987 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11300216,Human_RBP_ID_24853438 RMVar_hsa_circ_96352,RMVar_hsa_circ_113129,RMVar_hsa_circ_146967,RMVar_hsa_circ_146968,RMVar_hsa_circ_146971,RMVar_hsa_circ_355304,RMVar_hsa_circ_277321,RMVar_hsa_circ_89000,RMVar_hsa_circ_58897,RMVar_hsa_circ_146973,RMVar_hsa_circ_317308 13526 RMVar_ID_13526 Human_SNP_ID_450387688 A-to-I Human chr10 + 124803633 124803633 124803633 GATTCAAGTGACTCTTATTAGCTGGACACGGTAGCTCATGCCTGTAATCCCAGCACTTTGGGAGG GATTCAAGTGACTCTTATTAGCTGGACACGGTTGCTCATGCCTGTAATCCCAGCACTTTGGGAGG A T ABRAXAS2 Ensembl:ENSG00000165660 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1320752498 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125953,RMVar_hsa_circ_146976 13527 RMVar_ID_13527 Human_SNP_ID_450389769 A-to-I Human chr10 + 124811090 124811090 124811090 AAATACAAAAAATTAGCCGGACAGGCGCCTGTAGTCCCAGCTATGCGGGAGGCTGAGGCAGGAGA AAATACAAAAAATTAGCCGGACAGGCGCCTGTGGTCCCAGCTATGCGGGAGGCTGAGGCAGGAGA A G ABRAXAS2 Ensembl:ENSG00000165660 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs993688230 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2305,Human_RBP_ID_105576 RMVar_hsa_circ_125953,RMVar_hsa_circ_330794,RMVar_hsa_circ_146976,RMVar_hsa_circ_342724,RMVar_hsa_circ_277189,RMVar_hsa_circ_146977,RMVar_hsa_circ_146978 13528 RMVar_ID_13528 Human_SNP_ID_450390152 A-to-I Human chr10 + 124812598 124812598 124812598 CTAGGAGATTGAGGCTACAGTGAACTGTGATCATGCCACTGCACTCCAGCCTGGGTGATAGAGCA CTAGGAGATTGAGGCTACAGTGAACTGTGATCGTGCCACTGCACTCCAGCCTGGGTGATAGAGCA A G ABRAXAS2 Ensembl:ENSG00000165660 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs891401884 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125953,RMVar_hsa_circ_330794,RMVar_hsa_circ_146976,RMVar_hsa_circ_342724,RMVar_hsa_circ_277189,RMVar_hsa_circ_146977,RMVar_hsa_circ_146978 13529 RMVar_ID_13529 Human_SNP_ID_450416751 A-to-I Human chr10 + 124918230 124918230 124918230 TTTTGTATTTGAGACGGAGTTTCCCCCTTGTTACCCAGGCTGGAGTGCAGTGGCGCTATCTCGGC TTTTGTATTTGAGACGGAGTTTCCCCCTTGTTGCCCAGGCTGGAGTGCAGTGGCGCTATCTCGGC A G AL731577.2 Ensembl:ENSG00000249456 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1300454006 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11490472 13530 RMVar_ID_13530 Human_SNP_ID_450417083 A-to-I Human chr10 + 124919426 124919426 124919426 AAAATTTGCCGGGTATGGTGGCGTGTGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAAGAGA AAAATTTGCCGGGTATGGTGGCGTGTGCCTGTGATCCCAGCTACTCGGGAGGCTGAGGCAAGAGA A G AL731577.2 Ensembl:ENSG00000249456 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1184610931 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8245463 13531 RMVar_ID_13531 Human_SNP_ID_450418173 A-to-I Human chr10 + 124922592 124922592 124922592 TCAGCTCACTGCAACCTCCACCACCCGGCTTGAAGTGATTCTCCTGCCTCAGCCTTCTGAGTAGC TCAGCTCACTGCAACCTCCACCACCCGGCTTGGAGTGATTCTCCTGCCTCAGCCTTCTGAGTAGC A G AL731577.2 Ensembl:ENSG00000249456 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1282623931 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_146982 13532 RMVar_ID_13532 Human_SNP_ID_450418197 A-to-I Human chr10 + 124922679 124922679 124922679 CATGCCCAGCTCATTTTTTTGTATCTTTTAGTAGAGATGGGGTGTCACCGTGTTGGCCCGGCTGG CATGCCCAGCTCATTTTTTTGTATCTTTTAGTGGAGATGGGGTGTCACCGTGTTGGCCCGGCTGG A G AL731577.2 Ensembl:ENSG00000249456 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs553633545 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8245549,Human_RBP_ID_23442103 RMVar_hsa_circ_146982 13533 RMVar_ID_13533 Human_SNP_ID_450418397 A-to-I Human chr10 + 124923332 124923332 124923332 CAAACTAGCTGATGCCAGGTGCTGTGGCTCATACCTGTAATCCCAGCACTTTGGGAGGCCAAGGC CAAACTAGCTGATGCCAGGTGCTGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGC A G AL731577.2 Ensembl:ENSG00000249456 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs947005888 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_146982 13534 RMVar_ID_13534 Human_SNP_ID_450431948 A-to-I Human chr10 + 124977170 124977170 124977170 TTTTAAAATTTTTCTGTAGAGATGAGGTCCTCACTGTATTGCCCAGGCTGGTCTTGAACTCCCGG TTTTAAAATTTTTCTGTAGAGATGAGGTCCTCCCTGTATTGCCCAGGCTGGTCTTGAACTCCCGG A C ZRANB1 Ensembl:ENSG00000019995 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs975956954 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11302011 RMVar_hsa_circ_83361,RMVar_hsa_circ_83926,RMVar_hsa_circ_146991,RMVar_hsa_circ_92757,RMVar_hsa_circ_146994,RMVar_hsa_circ_146995 13535 RMVar_ID_13535 Human_SNP_ID_450474355 A-to-I Human chr10 - 125124101 125124101 125124101 GCACACTCCAGCTCTAGAACTTTCTTTGAGCAAGCTGGGTGTTGGAAGCCGGCCAGCCCAGCGTA GCACACTCCAGCTCTAGAACTTTCTTTGAGCATGCTGGGTGTTGGAAGCCGGCCAGCCCAGCGTA T A CTBP2 Ensembl:ENSG00000175029 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs940827366 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103784,RMVar_hsa_circ_147001,RMVar_hsa_circ_102505,RMVar_hsa_circ_147002,RMVar_hsa_circ_123269,RMVar_hsa_circ_286734,RMVar_hsa_circ_147006,RMVar_hsa_circ_147013,RMVar_hsa_circ_84575,RMVar_hsa_circ_147016 13536 RMVar_ID_13536 Human_SNP_ID_450480348 A-to-I Human chr10 - 125146080 125146080 125146080 GTCTCTTCTAGAAATACAAAAATTAGCCAGGTATGGTGGTTGGCACCTGTAATTCCAGCTAATCG GTCTCTTCTAGAAATACAAAAATTAGCCAGGTGTGGTGGTTGGCACCTGTAATTCCAGCTAATCG T C CTBP2 Ensembl:ENSG00000175029 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1247488688 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103784,RMVar_hsa_circ_147001,RMVar_hsa_circ_102505,RMVar_hsa_circ_147002 13537 RMVar_ID_13537 Human_SNP_ID_450480799 A-to-I Human chr10 - 125147769 125147769 125147769 TCTCAGCCTCCCAAGTAGGTGGGACTACAGGTACAGGGCACCACACCTGGCTAGTTTCTGTATTT TCTCAGCCTCCCAAGTAGGTGGGACTACAGGTGCAGGGCACCACACCTGGCTAGTTTCTGTATTT T C CTBP2 Ensembl:ENSG00000175029 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1250162565 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103784,RMVar_hsa_circ_147001,RMVar_hsa_circ_102505,RMVar_hsa_circ_147002 13538 RMVar_ID_13538 Human_SNP_ID_450480801 A-to-I Human chr10 - 125147775 125147775 125147775 TTCCCATCTCAGCCTCCCAAGTAGGTGGGACTACAGGTACAGGGCACCACACCTGGCTAGTTTCT TTCCCATCTCAGCCTCCCAAGTAGGTGGGACTGCAGGTACAGGGCACCACACCTGGCTAGTTTCT T C CTBP2 Ensembl:ENSG00000175029 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1235899701 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103784,RMVar_hsa_circ_147001,RMVar_hsa_circ_102505,RMVar_hsa_circ_147002 13539 RMVar_ID_13539 Human_SNP_ID_450611213 A-to-I Human chr10 - 125667332 125667332 125667332 ACCATGACTTGAAGCACTGCCAGTGTGTGACCAAGAAGGTGCTGACTGCTGTCTACAAGGCTCTG ACCATGACTTGAAGCACTGCCAGTGTGTGACCCAGAAGGTGCTGACTGCTGTCTACAAGGCTCTG T G TEX36,ALDOAP2 Ensembl:ENSG00000175018,Ensembl:ENSG00000214297 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs552912644 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_106282,Human_RBP_ID_19577223 13540 RMVar_ID_13540 Human_SNP_ID_450611359 A-to-I Human chr10 - 125667792 125667792 125667792 CGGCTGCAGTCCCTTAACGCCGAGAACACCAAAGAGAACTGGCGCTTCTACTGTCAGCTGCTGCT CGGCTGCAGTCCCTTAACGCCGAGAACACCAAGGAGAACTGGCGCTTCTACTGTCAGCTGCTGCT T C TEX36,ALDOAP2 Ensembl:ENSG00000175018,Ensembl:ENSG00000214297 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1035817811 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1911423 13541 RMVar_ID_13541 Human_SNP_ID_450611360 A-to-I Human chr10 - 125667794 125667794 125667794 AGCGGCTGCAGTCCCTTAACGCCGAGAACACCAAAGAGAACTGGCGCTTCTACTGTCAGCTGCTG AGCGGCTGCAGTCCCTTAACGCCGAGAACACCGAAGAGAACTGGCGCTTCTACTGTCAGCTGCTG T C TEX36,ALDOAP2 Ensembl:ENSG00000175018,Ensembl:ENSG00000214297 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs895869495 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1911423 13542 RMVar_ID_13542 Human_SNP_ID_450611367 A-to-I Human chr10 - 125667808 125667808 125667808 TGGGAGCATTGCCAAGCGGCTGCAGTCCCTTAACGCCGAGAACACCAAAGAGAACTGGCGCTTCT TGGGAGCATTGCCAAGCGGCTGCAGTCCCTTAGCGCCGAGAACACCAAAGAGAACTGGCGCTTCT T C TEX36,ALDOAP2 Ensembl:ENSG00000175018,Ensembl:ENSG00000214297 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs963347358 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19577224 Human_miRNA_ID_1824303,Human_miRNA_ID_1911423 13543 RMVar_ID_13543 Human_SNP_ID_450611388 A-to-I Human chr10 + 125667874 125667874 125667874 TGGACTCATCTGCAGCCAGGATGCCCTTGCCCAGTGCCACGATGCGGTGAGCGATGTCAGACAGC TGGACTCATCTGCAGCCAGGATGCCCTTGCCCGGTGCCACGATGCGGTGAGCGATGTCAGACAGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878903878 Functional Loss SNV dbSNP153 33..33 33 - - - 13544 RMVar_ID_13544 Human_SNP_ID_450611423 A-to-I Human chr10 + 125667981 125667981 125667981 ATGGTGCTGGTGGTGGCAAGTTCCAGTGCTTCAAAGGAAATTTCTTCCTTGGAAATCCAGACGGA ATGGTGCTGGTGGTGGCAAGTTCCAGTGCTTCGAAGGAAATTTCTTCCTTGGAAATCCAGACGGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334775658 Functional Loss SNV dbSNP153 33..33 33 - - - 13545 RMVar_ID_13545 Human_SNP_ID_450620512 A-to-I Human chr10 - 125703388 125703388 125703388 GCCATCTTGGCTCACTGCAAGCTCCGCCTCCCAGGTTCATGCCATTCTCCTGCCTCAGCCTCCCG GCCATCTTGGCTCACTGCAAGCTCCGCCTCCCGGGTTCATGCCATTCTCCTGCCTCAGCCTCCCG T C EDRF1-DT Ensembl:ENSG00000224023 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1478278817 Functional Loss SNV dbSNP153 33..33 33 - - - 13546 RMVar_ID_13546 Human_SNP_ID_450642763 A-to-I Human chr10 - 125792016 125792016 125792016 TTGCCTAGGCTGATCTCAAACTCCTGGCCTCAAGTAATCTTCCCACCTTGGCCTCCCAAAATGTA TTGCCTAGGCTGATCTCAAACTCCTGGCCTCAGGTAATCTTCCCACCTTGGCCTCCCAAAATGTA T C UROS Ensembl:ENSG00000188690 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs931135052 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32910,RMVar_hsa_circ_147033,RMVar_hsa_circ_96463,RMVar_hsa_circ_119673,RMVar_hsa_circ_128137,RMVar_hsa_circ_105354,RMVar_hsa_circ_89318,RMVar_hsa_circ_147034,RMVar_hsa_circ_147031,RMVar_hsa_circ_147032,RMVar_hsa_circ_147030 13547 RMVar_ID_13547 Human_SNP_ID_450643193 A-to-I Human chr10 - 125793818 125793818 125793818 GAGAGAGGCCGGGCGCTGTGGCTCCCACCTGGAATCCCAGCACTTTGGGAGGCCTCAGGCGGATC GAGAGAGGCCGGGCGCTGTGGCTCCCACCTGGGATCCCAGCACTTTGGGAGGCCTCAGGCGGATC T C UROS Ensembl:ENSG00000188690 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1485327719 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_373482,Human_RBP_ID_26398776 RMVar_hsa_circ_32910,RMVar_hsa_circ_147033,RMVar_hsa_circ_96463,RMVar_hsa_circ_119673,RMVar_hsa_circ_128137,RMVar_hsa_circ_105354,RMVar_hsa_circ_89318,RMVar_hsa_circ_147034,RMVar_hsa_circ_147031,RMVar_hsa_circ_147032,RMVar_hsa_circ_147030 13548 RMVar_ID_13548 Human_SNP_ID_450654583 A-to-I Human chr10 + 125837527 125837527 125837527 GTACCTCACTGCAGCCTTGACCTCCTGGGCTCAAGCGATCCTCTGTCGCAGAATCTCAAGTAGCT GTACCTCACTGCAGCCTTGACCTCCTGGGCTCGAGCGATCCTCTGTCGCAGAATCTCAAGTAGCT A G BCCIP Ensembl:ENSG00000107949 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348709869 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11306646 RMVar_hsa_circ_47309,RMVar_hsa_circ_377650 13549 RMVar_ID_13549 Human_SNP_ID_450659409 A-to-I Human chr10 - 125856938 125856938 125856938 TGTATTTATTTACTTAGAGACAGGACCTCACTATGTTGCCTAGGCTGGAGTGCAGTGGTGTGATC TGTATTTATTTACTTAGAGACAGGACCTCACTGTGTTGCCTAGGCTGGAGTGCAGTGGTGTGATC T C DHX32 Ensembl:ENSG00000089876 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1050542479 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11306809 RMVar_hsa_circ_14929,RMVar_hsa_circ_147047,RMVar_hsa_circ_147045,RMVar_hsa_circ_83949,RMVar_hsa_circ_323563,RMVar_hsa_circ_147048,RMVar_hsa_circ_81263,RMVar_hsa_circ_147049 13550 RMVar_ID_13550 Human_SNP_ID_450659410 A-to-I Human chr10 - 125856941 125856938 125856942 ATTTGTATTTATTTACTTAGAGACAGGACCTCACTATGTTGCCTAGGCTGGAGTGCAGTGGTGTG ATTTGTATTTATTTACTTAGAGACAGGACCT____ATGTTGCCTAGGCTGGAGTGCAGTGGTGTG TAGTG T DHX32 Ensembl:ENSG00000089876 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1452180746 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_11306809 RMVar_hsa_circ_14929,RMVar_hsa_circ_147047,RMVar_hsa_circ_147045,RMVar_hsa_circ_83949,RMVar_hsa_circ_323563,RMVar_hsa_circ_147048,RMVar_hsa_circ_81263,RMVar_hsa_circ_147049 13551 RMVar_ID_13551 Human_SNP_ID_450677044 A-to-I Human chr10 + 125916288 125916288 125916288 CGATCTCTTGACCCGCCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCACAC CGATCTCTTGACCCGCCTGCCTTGGCCTCCCAGAGTGCTGGGATTACAGGCATGAGCCACCACAC A G FANK1 Ensembl:ENSG00000203780 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1187736631 Functional Loss SNV dbSNP153 33..33 33 - - - 13552 RMVar_ID_13552 Human_SNP_ID_450930230 A-to-I Human chr10 + 126915662 126915662 126915662 GGTTAGTAACACGGGGTTTCACTGTGTTAGCCAGGATGGTCTCGATCTCCTGACCTCGTGATCTG GGTTAGTAACACGGGGTTTCACTGTGTTAGCCGGGATGGTCTCGATCTCCTGACCTCGTGATCTG A G DOCK1 Ensembl:ENSG00000150760 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs933650561 Functional Loss SNV dbSNP153 33..33 33 - - - 13553 RMVar_ID_13553 Human_SNP_ID_451758502 A-to-I Human chr10 - 130066460 130066460 130066460 GCCAGCTGCGTTGGTTCACACCTATAATCCCAAGACTTTGGGAGGCTAAGGCGAGTGGATCGCCT GCCAGCTGCGTTGGTTCACACCTATAATCCCAGGACTTTGGGAGGCTAAGGCGAGTGGATCGCCT T C C10orf143 Ensembl:ENSG00000237489 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1195985557 Functional Loss SNV dbSNP153 33..33 33 - - - 13554 RMVar_ID_13554 Human_SNP_ID_451758504 A-to-I Human chr10 - 130066467 130066467 130066467 GGTCTTGGCCAGCTGCGTTGGTTCACACCTATAATCCCAAGACTTTGGGAGGCTAAGGCGAGTGG GGTCTTGGCCAGCTGCGTTGGTTCACACCTATGATCCCAAGACTTTGGGAGGCTAAGGCGAGTGG T C C10orf143 Ensembl:ENSG00000237489 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs557006969 Functional Loss SNV dbSNP153 33..33 33 - - - 13555 RMVar_ID_13555 Human_SNP_ID_451767376 A-to-I Human chr10 - 130105614 130105614 130105614 GCGATTCTCTTGCCTTAGCCTCCGGAGTAGCTAGAATTACAGGTGCCCGCCACCATGCCCAGCTA GCGATTCTCTTGCCTTAGCCTCCGGAGTAGCTGGAATTACAGGTGCCCGCCACCATGCCCAGCTA T C C10orf143 Ensembl:ENSG00000237489 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1564971903 Functional Loss SNV dbSNP153 33..33 33 - - - 13556 RMVar_ID_13556 Human_SNP_ID_451777243 A-to-I Human chr10 + 130139750 130139750 130139750 GGCCAGGAGTTTGAGAGTAGCTTGAACAACATAGAACCCATCTCTACAAAAAATAAAAAAAGTAG GGCCAGGAGTTTGAGAGTAGCTTGAACAACATGGAACCCATCTCTACAAAAAATAAAAAAAGTAG A G GLRX3 Ensembl:ENSG00000108010 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1408476101 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11309448 RMVar_hsa_circ_79780,RMVar_hsa_circ_147211 13557 RMVar_ID_13557 Human_SNP_ID_451777559 A-to-I Human chr10 + 130141131 130141131 130141131 GGCGAATGCAGGCAGATTGATTGCTTGAGCCCAGGAGTTTGAGACCAGCCTGGTCATTGGCCAAA GGCGAATGCAGGCAGATTGATTGCTTGAGCCCGGGAGTTTGAGACCAGCCTGGTCATTGGCCAAA A G GLRX3 Ensembl:ENSG00000108010 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893422498 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79780,RMVar_hsa_circ_147211 13558 RMVar_ID_13558 Human_SNP_ID_451778668 A-to-I Human chr10 + 130145498 130145498 130145498 CAGCCCAGCCAACATAGTGAAACCCTGTCTCTACTAAAATACAAAAATTAGCTGGGCGTGGTGGC CAGCCCAGCCAACATAGTGAAACCCTGTCTCTGCTAAAATACAAAAATTAGCTGGGCGTGGTGGC A G GLRX3 Ensembl:ENSG00000108010 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs757475220 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24794339 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 13559 RMVar_ID_13559 Human_SNP_ID_451779335 A-to-I Human chr10 + 130148272 130148272 130148272 TCTCCACCTTAGCCTCCCGAATAGCTGGGACTATAGGTGTACACCCCTGCCCAGCTAATTTTTGT TCTCCACCTTAGCCTCCCGAATAGCTGGGACTCTAGGTGTACACCCCTGCCCAGCTAATTTTTGT A C GLRX3 Ensembl:ENSG00000108010 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs775101307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17559230 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 13560 RMVar_ID_13560 Human_SNP_ID_451779336 A-to-I Human chr10 + 130148272 130148272 130148272 TCTCCACCTTAGCCTCCCGAATAGCTGGGACTATAGGTGTACACCCCTGCCCAGCTAATTTTTGT TCTCCACCTTAGCCTCCCGAATAGCTGGGACTGTAGGTGTACACCCCTGCCCAGCTAATTTTTGT A G GLRX3 Ensembl:ENSG00000108010 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs775101307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17559230 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 13561 RMVar_ID_13561 Human_SNP_ID_451779354 A-to-I Human chr10 + 130148331 130148331 130148331 TTTTGTATTTTTTGTAGCGATACGGTTTCACCATGTTGCTCAGGCTGGTCTTGAACTCATGGGCT TTTTGTATTTTTTGTAGCGATACGGTTTCACCGTGTTGCTCAGGCTGGTCTTGAACTCATGGGCT A G GLRX3 Ensembl:ENSG00000108010 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1288472007 Functional Loss SNV dbSNP153 33..33 33 - - - 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 13562 RMVar_ID_13562 Human_SNP_ID_451782942 A-to-I Human chr10 + 130162077 130162077 130162077 CAGTGCGACGGAACCTCTGTCTACTAGGGGTCAAGCGATTCTCCTGTCTCAGCCTCCCGAGTAGC CAGTGCGACGGAACCTCTGTCTACTAGGGGTCGAGCGATTCTCCTGTCTCAGCCTCCCGAGTAGC A G GLRX3 Ensembl:ENSG00000108010 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs888132736 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_147219,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_291591,RMVar_hsa_circ_97963,RMVar_hsa_circ_147213,RMVar_hsa_circ_147215,RMVar_hsa_circ_55682,RMVar_hsa_circ_147214,RMVar_hsa_circ_299341,RMVar_hsa_circ_369808,RMVar_hsa_circ_377063,RMVar_hsa_circ_356974,RMVar_hsa_circ_328350,RMVar_hsa_circ_86945,RMVar_hsa_circ_298142,RMVar_hsa_circ_147220,RMVar_hsa_circ_147221,RMVar_hsa_circ_147217,RMVar_hsa_circ_147218 13563 RMVar_ID_13563 Human_SNP_ID_451782943 A-to-I Human chr10 + 130162077 130162077 130162077 CAGTGCGACGGAACCTCTGTCTACTAGGGGTCAAGCGATTCTCCTGTCTCAGCCTCCCGAGTAGC CAGTGCGACGGAACCTCTGTCTACTAGGGGTCTAGCGATTCTCCTGTCTCAGCCTCCCGAGTAGC A T GLRX3 Ensembl:ENSG00000108010 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs888132736 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_147219,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_291591,RMVar_hsa_circ_97963,RMVar_hsa_circ_147213,RMVar_hsa_circ_147215,RMVar_hsa_circ_55682,RMVar_hsa_circ_147214,RMVar_hsa_circ_299341,RMVar_hsa_circ_369808,RMVar_hsa_circ_377063,RMVar_hsa_circ_356974,RMVar_hsa_circ_328350,RMVar_hsa_circ_86945,RMVar_hsa_circ_298142,RMVar_hsa_circ_147220,RMVar_hsa_circ_147221,RMVar_hsa_circ_147217,RMVar_hsa_circ_147218 13564 RMVar_ID_13564 Human_SNP_ID_451788567 A-to-I Human chr10 + 130184432 130184432 130184432 CTTGTAATCCCAGCACTTTGGGAGGCGGAGGCAGGCGGGTTGCTTGAGCTCCGGAGCTTGAGACC CTTGTAATCCCAGCACTTTGGGAGGCGGAGGCGGGCGGGTTGCTTGAGCTCCGGAGCTTGAGACC A G GLRX3 Ensembl:ENSG00000108010 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1316783757 Functional Loss SNV dbSNP153 33..33 33 - - - 13565 RMVar_ID_13565 Human_SNP_ID_451788606 A-to-I Human chr10 + 130184585 130184585 130184585 GGGGAGCTGAGATGGGAGGATTGCTTGAGCCCAGGAGGTCAAGGCTGCAGTGATCGTGCCATTGC GGGGAGCTGAGATGGGAGGATTGCTTGAGCCCGGGAGGTCAAGGCTGCAGTGATCGTGCCATTGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs539572450 Functional Loss SNV dbSNP153 33..33 33 - - - 13566 RMVar_ID_13566 Human_SNP_ID_452266219 A-to-I Human chr10 + 131949523 131949523 131949523 CACAGGTGAAAATTACCAAGCACATACAGGAAAAGCCACCGTGAGCAAGTCAGCAGAACCACAGC CACAGGTGAAAATTACCAAGCACATACAGGAAGAGCCACCGTGAGCAAGTCAGCAGAACCACAGC A G PPP2R2D Ensembl:ENSG00000175470 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1215438386 Functional Loss SNV dbSNP153 33..33 33 - - - 13567 RMVar_ID_13567 Human_SNP_ID_452269901 A-to-I Human chr10 - 131959411 131959374 131959411 CATCTCCACAGGGGGATGGGGGATCAGCACACACCTTCATCTCCACAGTGGGATGGCGGATCAGC CATCTCCACAGGGGGATGGGGGATCAGCACAC_________________________________ CGTGTGCTGATCCGCCATCCCACTGTGGAGATGAAGGT C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1554901043 Functional Loss DEL dbSNP153 33..65 33 - - - 13568 RMVar_ID_13568 Human_SNP_ID_452269929 A-to-I Human chr10 - 131959411 131959411 131959411 CATCTCCACAGGGGGATGGGGGATCAGCACACACCTTCATCTCCACAGTGGGATGGCGGATCAGC CATCTCCACAGGGGGATGGGGGATCAGCACACGCCTTCATCTCCACAGTGGGATGGCGGATCAGC T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1286737612 Functional Loss SNV dbSNP153 33..33 33 - - - 13569 RMVar_ID_13569 Human_SNP_ID_452269930 A-to-I Human chr10 - 131959411 131959411 131959411 CATCTCCACAGGGGGATGGGGGATCAGCACACACCTTCATCTCCACAGTGGGATGGCGGATCAGC CATCTCCACAGGGGGATGGGGGATCAGCACACCCCTTCATCTCCACAGTGGGATGGCGGATCAGC T G - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1286737612 Functional Loss SNV dbSNP153 33..33 33 - - - 13570 RMVar_ID_13570 Human_SNP_ID_452271849 A-to-I Human chr10 + 131965689 131965689 131965689 GCTGATCGCGAACTCCTGAGCCCAGGCAATCCACCCGCCCCAGCCTCCCAAAGTGCTGGGATTAC GCTGATCGCGAACTCCTGAGCCCAGGCAATCCCCCCGCCCCAGCCTCCCAAAGTGCTGGGATTAC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1554902127 Functional Loss SNV dbSNP153 33..33 33 - - - 13571 RMVar_ID_13571 Human_SNP_ID_452383259 A-to-I Human chr10 - 132330940 132330940 132330940 CCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGTGCCCGGCCTGATTCCACTTTT CCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGTGCCCGGCCTGATTCCACTTTT T C STK32C Ensembl:ENSG00000165752 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs918525618 Functional Loss SNV dbSNP153 33..33 33 - - - 13572 RMVar_ID_13572 Human_SNP_ID_452657048 A-to-I Human chr10 + 133207173 133207173 133207173 TGTACGCGGAACGCTGGGGCCTGGAGCCCTGCACCCTCCCAGTGATCGTGAACATCGCGGCCGCA TGTACGCGGAACGCTGGGGCCTGGAGCCCTGCGCCCTCCCAGTGATCGTGAACATCGCGGCCGCA A G KNDC1 Ensembl:ENSG00000171798 Protein coding CDS GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1321312316 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103909,RMVar_hsa_circ_120446,RMVar_hsa_circ_147291,RMVar_hsa_circ_88527,RMVar_hsa_circ_147292,RMVar_hsa_circ_127766,RMVar_hsa_circ_147293,RMVar_hsa_circ_147294 13573 RMVar_ID_13573 Human_SNP_ID_452677701 A-to-I Human chr10 - 133265735 133265735 133265735 GGAGTGCAGTGGCGCGATCTCAGCTCACTGCAATCTCCGCCTCTCAGGTTCATGCCATTCTCCTG GGAGTGCAGTGGCGCGATCTCAGCTCACTGCAGTCTCCGCCTCTCAGGTTCATGCCATTCTCCTG T C ADAM8 Ensembl:ENSG00000151651 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs979042293 Functional Loss SNV dbSNP153 33..33 33 - - - 13574 RMVar_ID_13574 Human_SNP_ID_452689405 A-to-I Human chr10 - 133296660 133296660 133296660 CCAGCCTGGGCGACAGGACGAGACTAGTCTCTACAAAAAATGTGAAAATTAGCCGAGTGTGGTAG CCAGCCTGGGCGACAGGACGAGACTAGTCTCTCCAAAAAATGTGAAAATTAGCCGAGTGTGGTAG T G TUBGCP2 Ensembl:ENSG00000130640 Protein coding intron GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs968580966 Functional Loss SNV dbSNP153 33..33 33 - - - 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_147304 13575 RMVar_ID_13575 Human_SNP_ID_452689599 A-to-I Human chr10 - 133297389 133297389 133297389 TTTTTATTTATTTTTAGTTCTTTTGAGATGGAATCTCGCTCTGTCGCCCAGGCTGAAGTGCAGTG TTTTTATTTATTTTTAGTTCTTTTGAGATGGACTCTCGCTCTGTCGCCCAGGCTGAAGTGCAGTG T G TUBGCP2 Ensembl:ENSG00000130640 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs760447640 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_Splice_Rec_1191050,Human_Splice_Rec_1191051 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_124783,RMVar_hsa_circ_147304,RMVar_hsa_circ_147305 13576 RMVar_ID_13576 Human_SNP_ID_452690578 A-to-I Human chr10 - 133300498 133300498 133300498 ACGATCTTGTCTTACTGCAGTCTCAACCTCCCAGGCTGATGTGATCCTCCCATCTCAGCTTCCCA ACGATCTTGTCTTACTGCAGTCTCAACCTCCCGGGCTGATGTGATCCTCCCATCTCAGCTTCCCA T C TUBGCP2 Ensembl:ENSG00000130640 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs552044006 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1191168 RMVar_hsa_circ_6933,RMVar_hsa_circ_119302,RMVar_hsa_circ_147301,RMVar_hsa_circ_329236,RMVar_hsa_circ_347940,RMVar_hsa_circ_302694,RMVar_hsa_circ_147306 13577 RMVar_ID_13577 Human_SNP_ID_452690606 A-to-I Human chr10 - 133300569 133300569 133300569 CGGATAAGGTTTGTTTTGTTTTGTTTTGAGACAGAGTCTTACTCTGTCACCCAGGCTGGAATGCA CGGATAAGGTTTGTTTTGTTTTGTTTTGAGACGGAGTCTTACTCTGTCACCCAGGCTGGAATGCA T C TUBGCP2 Ensembl:ENSG00000130640 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1185962772 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6933,RMVar_hsa_circ_119302,RMVar_hsa_circ_147301,RMVar_hsa_circ_329236,RMVar_hsa_circ_347940,RMVar_hsa_circ_302694,RMVar_hsa_circ_147306 13578 RMVar_ID_13578 Human_SNP_ID_452692048 A-to-I Human chr10 - 133305042 133305042 133305042 TCCACAAGAGTTGGAGGCGTAGAGTCTTCTCTAAACTCTCCGGGGAAAGGGAGACTCCCTTTCCC TCCACAAGAGTTGGAGGCGTAGAGTCTTCTCTGAACTCTCCGGGGAAAGGGAGACTCCCTTTCCC T C TUBGCP2 Ensembl:ENSG00000130640 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1306733003 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91092,RMVar_hsa_circ_147308 13579 RMVar_ID_13579 Human_SNP_ID_452718551 A-to-I Human chr10 + 133387234 133387234 133387234 CCAGGAGGCGGAGGTTGCAGTGAGCTGTGATCAAGCCACTGAACTCCAGCCTGGGCAACAGAGGG CCAGGAGGCGGAGGTTGCAGTGAGCTGTGATCGAGCCACTGAACTCCAGCCTGGGCAACAGAGGG A G AL360181.3,PAOX Ensembl:ENSG00000254536,Ensembl:ENSG00000148832 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs923180093 Functional Loss SNV dbSNP153 33..33 33 - - - 13580 RMVar_ID_13580 Human_SNP_ID_474516391 A-to-I Human chr11 - 82839397 82839397 82839397 ACAGGTAGTGTGCCAGTATTTGAAAAATCCCAATGTATCTGATTCACTGCTGCTGCAGAATATTT ACAGGTAGTGTGCCAGTATTTGAAAAATCCCAGTGTATCTGATTCACTGCTGCTGCAGAATATTT T C PRCP Ensembl:ENSG00000137509 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs779113626 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_404804,Human_RBP_ID_3381118,Human_RBP_ID_17802131,Human_RBP_ID_22753785 Human_Splice_Rec_1282654,Human_Splice_Rec_1282672,Human_Splice_Rec_1282688,Human_Splice_Rec_1282700,Human_Splice_Rec_1282712 Human_miRNA_ID_2106562,Human_miRNA_ID_2165054 RMVar_hsa_circ_14317,RMVar_hsa_circ_109821,RMVar_hsa_circ_152127,RMVar_hsa_circ_81966,RMVar_hsa_circ_152128,RMVar_hsa_circ_372378,RMVar_hsa_circ_323256,RMVar_hsa_circ_152129,RMVar_hsa_circ_152130 13581 RMVar_ID_13581 Human_SNP_ID_474570401 A-to-I Human chr11 + 83074527 83074458 83074528 CAAAAAAGAATTAGGGCCAGGCACAGTGGCTGACACCTGTAATCCTAGCACTTTGGGAGGCCGAG __________________________________ACCTGTAATCCTAGCACTTTGGGAGGCCGAG TTAGGAATATCTAGAGGAGGTAAAGCTTTTCATCTCTCAAAAAAGAATTAGGGCCAGGCACAGTGGCTGAC T RAB30-DT Ensembl:ENSG00000246067 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1565297407 Functional Loss DEL dbSNP153 1..34 33 - - - 13582 RMVar_ID_13582 Human_SNP_ID_474570576 A-to-I Human chr11 + 83075249 83075249 83075249 TCAGTTTTAGCTTTAAGAGGACCAACCGGGCCAAGCACGGTGGCTCACGCCTGTAATCCCAGCAC TCAGTTTTAGCTTTAAGAGGACCAACCGGGCCGAGCACGGTGGCTCACGCCTGTAATCCCAGCAC A G RAB30-DT Ensembl:ENSG00000246067 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1004283153 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_752481,Human_RBP_ID_6098989 13583 RMVar_ID_13583 Human_SNP_ID_474570624 A-to-I Human chr11 + 83075413 83075413 83075413 GAGTGTGGTGGCGGGTGCCTGTAATCCCAGCGACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAA GAGTGTGGTGGCGGGTGCCTGTAATCCCAGCGTCTTGGGAGGCTGAGGCAGGAGAATCGCTTGAA A T RAB30-DT Ensembl:ENSG00000246067 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs539152247 Functional Loss SNV dbSNP153 33..33 33 - - - 13584 RMVar_ID_13584 Human_SNP_ID_474572159 A-to-I Human chr11 + 83081626 83081622 83081626 ACCTCCGCCTCCTGGATTCAGGCAGTTCCCCCACCCCACCCTCCCGAGTAGCAGAGACGGGGTTT ACCTCCGCCTCCTGGATTCAGGCAGTTCC____CCCCACCCTCCCGAGTAGCAGAGACGGGGTTT CCCCA C RAB30-DT Ensembl:ENSG00000246067 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs916842175 Functional Loss DEL dbSNP153 30..33 33 - - - 13585 RMVar_ID_13585 Human_SNP_ID_474572160 A-to-I Human chr11 + 83081626 83081626 83081626 ACCTCCGCCTCCTGGATTCAGGCAGTTCCCCCACCCCACCCTCCCGAGTAGCAGAGACGGGGTTT ACCTCCGCCTCCTGGATTCAGGCAGTTCCCCCCCCCCACCCTCCCGAGTAGCAGAGACGGGGTTT A C RAB30-DT Ensembl:ENSG00000246067 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs907188897 Functional Loss SNV dbSNP153 33..33 33 - - - 13586 RMVar_ID_13586 Human_SNP_ID_474572199 A-to-I Human chr11 + 83081722 83081722 83081722 TGACCTTGTGGTCTGCCCGCCTCGGCCCCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCAC TGACCTTGTGGTCTGCCCGCCTCGGCCCCCCAGAGTGCTGGGATTACAGGCGTGAGCCACCGCAC A G RAB30-DT Ensembl:ENSG00000246067 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900431593 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1283025,Human_Splice_Rec_1283027 13587 RMVar_ID_13587 Human_SNP_ID_474572730 A-to-I Human chr11 + 83083357 83083357 83083357 CTGTCTCTTAAAAATATATATTTTGGGGAGCCAGGTGTGGCACCTCACGCCTGTAATCCCAACAC CTGTCTCTTAAAAATATATATTTTGGGGAGCCCGGTGTGGCACCTCACGCCTGTAATCCCAACAC A C RAB30-DT Ensembl:ENSG00000246067 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1019635350 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6099074,Human_RBP_ID_8246868,Human_RBP_ID_11730822,Human_RBP_ID_17559729 13588 RMVar_ID_13588 Human_SNP_ID_474572818 A-to-I Human chr11 + 83083589 83083589 83083589 TTGAGCCTAGGAGGTGGAGGTTGGAGTACGCCAAGATCACACCACTGCATTCCAGCCTTGGTGTC TTGAGCCTAGGAGGTGGAGGTTGGAGTACGCCGAGATCACACCACTGCATTCCAGCCTTGGTGTC A G RAB30-DT Ensembl:ENSG00000246067 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474821403 Functional Loss SNV dbSNP153 33..33 33 - - - 13589 RMVar_ID_13589 Human_SNP_ID_474573203 A-to-I Human chr11 + 83085091 83085091 83085091 CAGGGAGGCAAAGATTGCTGTGAGCTGAGATCACGCCACTGCACTCCAGCCTGGGCAACAGAGCC CAGGGAGGCAAAGATTGCTGTGAGCTGAGATCGCGCCACTGCACTCCAGCCTGGGCAACAGAGCC A G RAB30-DT Ensembl:ENSG00000246067 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910914879 Functional Loss SNV dbSNP153 33..33 33 - - - 13590 RMVar_ID_13590 Human_SNP_ID_474573550 A-to-I Human chr11 + 83086584 83086584 83086584 CTCCTGCCTCAGCCTCTGGAGTAGCCAGGACTACGCACTGCGCCACCACACCCAGCTAATTTTGT CTCCTGCCTCAGCCTCTGGAGTAGCCAGGACTGCGCACTGCGCCACCACACCCAGCTAATTTTGT A G RAB30-DT Ensembl:ENSG00000246067 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1288199894 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11730895 13591 RMVar_ID_13591 Human_SNP_ID_474574757 A-to-I Human chr11 + 83091425 83091425 83091425 AAAATTAGCCTGGCATGGTGGCACACACCTGTAATTCCAGCTGCTCGGGAGGCTGAAGCATGAGA AAAATTAGCCTGGCATGGTGGCACACACCTGTGATTCCAGCTGCTCGGGAGGCTGAAGCATGAGA A G RAB30-DT Ensembl:ENSG00000246067 lincRNA intron GSE38233;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;ASD brains,Fragile X samples from NIH NeuroBioBank;Bronchiolar epithelium,BEP2D cell line - 24183664,30559470,31158229 RNA-Seq:(High) rs1325191574 Functional Loss SNV dbSNP153 33..33 33 - - - 13592 RMVar_ID_13592 Human_SNP_ID_474574768 A-to-I Human chr11 + 83091478 83091478 83091478 TGAAGCATGAGAATCACTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCCAAGGTTGCAGTGGATC TGAAGCATGAGAATCACTTGAACCTGGGAGGCGGAGGTTGCAGTGAGCCAAGGTTGCAGTGGATC A G RAB30-DT Ensembl:ENSG00000246067 lincRNA intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs767375803 Functional Loss SNV dbSNP153 33..33 33 - - - 13593 RMVar_ID_13593 Human_SNP_ID_474578846 A-to-I Human chr11 - 83108099 83108099 83108099 CAAAAATTAGCCGGACGTGGTAGTGCATGCCTATAGTCCCAGCTACTCAGGAGGCTGAGGCAGGA CAAAAATTAGCCGGACGTGGTAGTGCATGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1441384514 Functional Loss SNV dbSNP153 33..33 33 - - - 13594 RMVar_ID_13594 Human_SNP_ID_474596498 A-to-I Human chr11 + 83175191 83175191 83175191 GTCTTCTTGCTCTTTTGTCCAGGCTGGAGTACAGTGGGGTGATCTTGGCTCACTGCAACCTCCTC GTCTTCTTGCTCTTTTGTCCAGGCTGGAGTACGGTGGGGTGATCTTGGCTCACTGCAACCTCCTC A G PCF11 Ensembl:ENSG00000165494 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs920489263 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20232,RMVar_hsa_circ_269664,RMVar_hsa_circ_360101,RMVar_hsa_circ_364672,RMVar_hsa_circ_152143,RMVar_hsa_circ_48414,RMVar_hsa_circ_152142,RMVar_hsa_circ_323653,RMVar_hsa_circ_22255,RMVar_hsa_circ_41487,RMVar_hsa_circ_152150,RMVar_hsa_circ_83861,RMVar_hsa_circ_65648,RMVar_hsa_circ_152153,RMVar_hsa_circ_67180,RMVar_hsa_circ_55359 13595 RMVar_ID_13595 Human_SNP_ID_474596589 A-to-I Human chr11 + 83175608 83175608 83175608 CCCCGTCTCTACTAAAAATACAAAAAGAAATTAGCTGGGTGTGGTGGCACGCACCTGTAGTCCAG CCCCGTCTCTACTAAAAATACAAAAAGAAATTGGCTGGGTGTGGTGGCACGCACCTGTAGTCCAG A G PCF11 Ensembl:ENSG00000165494 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1321544377 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20232,RMVar_hsa_circ_269664,RMVar_hsa_circ_360101,RMVar_hsa_circ_364672,RMVar_hsa_circ_152143,RMVar_hsa_circ_48414,RMVar_hsa_circ_152142,RMVar_hsa_circ_323653,RMVar_hsa_circ_22255,RMVar_hsa_circ_41487,RMVar_hsa_circ_152150,RMVar_hsa_circ_83861,RMVar_hsa_circ_65648,RMVar_hsa_circ_152153,RMVar_hsa_circ_67180,RMVar_hsa_circ_55359 13596 RMVar_ID_13596 Human_SNP_ID_474597214 A-to-I Human chr11 + 83178185 83178185 83178185 GGGATTACAGGTGTGCACCACCATACCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCA GGGATTACAGGTGTGCACCACCATACCCAGCTTATTTTTGTATTTTTAGTAGAGATGGGGTTTCA A T PCF11 Ensembl:ENSG00000165494 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs905959802 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20232,RMVar_hsa_circ_269664,RMVar_hsa_circ_360101,RMVar_hsa_circ_152142,RMVar_hsa_circ_55359,RMVar_hsa_circ_368944 13597 RMVar_ID_13597 Human_SNP_ID_474597231 A-to-I Human chr11 + 83178248 83178248 83178248 CACCACGTTGGCCAGGCTAGTCTCGAACTCCTAACCTCCAGTGATCCACCTGCCTTGGCCTCCCA CACCACGTTGGCCAGGCTAGTCTCGAACTCCTGACCTCCAGTGATCCACCTGCCTTGGCCTCCCA A G PCF11 Ensembl:ENSG00000165494 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs775454540 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20232,RMVar_hsa_circ_269664,RMVar_hsa_circ_360101,RMVar_hsa_circ_152142,RMVar_hsa_circ_55359,RMVar_hsa_circ_368944 13598 RMVar_ID_13598 Human_SNP_ID_474597301 A-to-I Human chr11 + 83178567 83178567 83178567 CCTGTAATCCCAGCACTTTGTAAGGCCGAGGCAGGTGGATCACGAGGTCAGGAGATCGAGACCAT CCTGTAATCCCAGCACTTTGTAAGGCCGAGGCGGGTGGATCACGAGGTCAGGAGATCGAGACCAT A G PCF11 Ensembl:ENSG00000165494 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1354657709 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20232,RMVar_hsa_circ_269664,RMVar_hsa_circ_360101,RMVar_hsa_circ_152142,RMVar_hsa_circ_55359,RMVar_hsa_circ_368944 13599 RMVar_ID_13599 Human_SNP_ID_474597504 A-to-I Human chr11 + 83179281 83179277 83179281 TCTTTTTCCTTTTTTTTTTGAGACAGAGTCTCACTCTGTCACCCAGGCTAGAGTGCAGTGGCCCT TCTTTTTCCTTTTTTTTTTGAGACAGAGT____CTCTGTCACCCAGGCTAGAGTGCAGTGGCCCT TCTCA T PCF11 Ensembl:ENSG00000165494 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1405374256 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_20232,RMVar_hsa_circ_269664,RMVar_hsa_circ_360101,RMVar_hsa_circ_152142,RMVar_hsa_circ_55359,RMVar_hsa_circ_368944 13600 RMVar_ID_13600 Human_SNP_ID_474597531 A-to-I Human chr11 + 83179411 83179411 83179411 AGCTAAGATTATAGGCACCCATCACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGT AGCTAAGATTATAGGCACCCATCACCACGCCCGGCTAATTTTTGTATTTTTAGTAGAGATGGGGT A G PCF11 Ensembl:ENSG00000165494 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1386334912 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20232,RMVar_hsa_circ_269664,RMVar_hsa_circ_360101,RMVar_hsa_circ_152142,RMVar_hsa_circ_55359,RMVar_hsa_circ_368944 13601 RMVar_ID_13601 Human_SNP_ID_474597549 A-to-I Human chr11 + 83179484 83179484 83179484 GTTGTCCAGGCTGTTCTCGAACTCCTGGGCTCAAGTCATCTGCCCGCCTCGGCCTTCCAAAATGC GTTGTCCAGGCTGTTCTCGAACTCCTGGGCTCGAGTCATCTGCCCGCCTCGGCCTTCCAAAATGC A G PCF11 Ensembl:ENSG00000165494 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs957101780 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20232,RMVar_hsa_circ_269664,RMVar_hsa_circ_360101,RMVar_hsa_circ_152142,RMVar_hsa_circ_55359,RMVar_hsa_circ_368944 13602 RMVar_ID_13602 Human_SNP_ID_474597604 A-to-I Human chr11 + 83179694 83179694 83179694 GGGAGGCTGAGGTGGGCAGATCACCTGAGGTCAGGAGTTCAAGACCAGCTTGGCCAACATGGTAA GGGAGGCTGAGGTGGGCAGATCACCTGAGGTCTGGAGTTCAAGACCAGCTTGGCCAACATGGTAA A T PCF11 Ensembl:ENSG00000165494 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs898235979 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20232,RMVar_hsa_circ_269664,RMVar_hsa_circ_360101,RMVar_hsa_circ_152142,RMVar_hsa_circ_55359,RMVar_hsa_circ_368944 13603 RMVar_ID_13603 Human_SNP_ID_474597620 A-to-I Human chr11 + 83179752 83179752 83179752 ATGGTAACATGTCTCTACTAGAACCTGTCTCTACTAGAAATACTAAAATTAGCTGGGCGTGGTAG ATGGTAACATGTCTCTACTAGAACCTGTCTCTGCTAGAAATACTAAAATTAGCTGGGCGTGGTAG A G PCF11 Ensembl:ENSG00000165494 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1054879377 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20232,RMVar_hsa_circ_269664,RMVar_hsa_circ_360101,RMVar_hsa_circ_152142,RMVar_hsa_circ_55359,RMVar_hsa_circ_368944 13604 RMVar_ID_13604 Human_SNP_ID_474597621 A-to-I Human chr11 + 83179755 83179755 83179755 GTAACATGTCTCTACTAGAACCTGTCTCTACTAGAAATACTAAAATTAGCTGGGCGTGGTAGTGG GTAACATGTCTCTACTAGAACCTGTCTCTACTGGAAATACTAAAATTAGCTGGGCGTGGTAGTGG A G PCF11 Ensembl:ENSG00000165494 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs558902710 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20232,RMVar_hsa_circ_269664,RMVar_hsa_circ_360101,RMVar_hsa_circ_152142,RMVar_hsa_circ_55359,RMVar_hsa_circ_368944 13605 RMVar_ID_13605 Human_SNP_ID_474597629 A-to-I Human chr11 + 83179790 83179790 83179790 AATACTAAAATTAGCTGGGCGTGGTAGTGGGCACTTGTAATCCCAGCTACTCGGGAGGCTGAGGT AATACTAAAATTAGCTGGGCGTGGTAGTGGGCCCTTGTAATCCCAGCTACTCGGGAGGCTGAGGT A C PCF11 Ensembl:ENSG00000165494 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1320039814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24905440 RMVar_hsa_circ_20232,RMVar_hsa_circ_269664,RMVar_hsa_circ_360101,RMVar_hsa_circ_152142,RMVar_hsa_circ_55359,RMVar_hsa_circ_368944 13606 RMVar_ID_13606 Human_SNP_ID_474597630 A-to-I Human chr11 + 83179790 83179790 83179790 AATACTAAAATTAGCTGGGCGTGGTAGTGGGCACTTGTAATCCCAGCTACTCGGGAGGCTGAGGT AATACTAAAATTAGCTGGGCGTGGTAGTGGGCGCTTGTAATCCCAGCTACTCGGGAGGCTGAGGT A G PCF11 Ensembl:ENSG00000165494 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1320039814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24905440 RMVar_hsa_circ_20232,RMVar_hsa_circ_269664,RMVar_hsa_circ_360101,RMVar_hsa_circ_152142,RMVar_hsa_circ_55359,RMVar_hsa_circ_368944 13607 RMVar_ID_13607 Human_SNP_ID_474597635 A-to-I Human chr11 + 83179802 83179802 83179802 AGCTGGGCGTGGTAGTGGGCACTTGTAATCCCAGCTACTCGGGAGGCTGAGGTGGGGAGAATTGC AGCTGGGCGTGGTAGTGGGCACTTGTAATCCCGGCTACTCGGGAGGCTGAGGTGGGGAGAATTGC A G PCF11 Ensembl:ENSG00000165494 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1247057724 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20232,RMVar_hsa_circ_269664,RMVar_hsa_circ_360101,RMVar_hsa_circ_152142,RMVar_hsa_circ_55359,RMVar_hsa_circ_368944 13608 RMVar_ID_13608 Human_SNP_ID_474598631 A-to-I Human chr11 + 83183751 83183751 83183751 ACCTCAAGTGATCCACCCACCTTGGCCTCCCAAAGTGCTAGGATTATAGGCGTGAGCCACCGTGC ACCTCAAGTGATCCACCCACCTTGGCCTCCCAGAGTGCTAGGATTATAGGCGTGAGCCACCGTGC A G PCF11,AP000873.4 Ensembl:ENSG00000165494,Ensembl:ENSG00000254676 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs144528983 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269664,RMVar_hsa_circ_152142 13609 RMVar_ID_13609 Human_SNP_ID_474598632 A-to-I Human chr11 + 83183758 83183758 83183758 GTGATCCACCCACCTTGGCCTCCCAAAGTGCTAGGATTATAGGCGTGAGCCACCGTGCTCGGCCA GTGATCCACCCACCTTGGCCTCCCAAAGTGCTGGGATTATAGGCGTGAGCCACCGTGCTCGGCCA A G PCF11,AP000873.4 Ensembl:ENSG00000165494,Ensembl:ENSG00000254676 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1022359888 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269664,RMVar_hsa_circ_152142 13610 RMVar_ID_13610 Human_SNP_ID_474598712 A-to-I Human chr11 + 83184077 83184077 83184077 GTGAGGCTGAGGCAGGAGAATTGTTTGAATCCAGGAGGTGGAGGTTGCAGTGAGCTGAGTTCATG GTGAGGCTGAGGCAGGAGAATTGTTTGAATCCGGGAGGTGGAGGTTGCAGTGAGCTGAGTTCATG A G PCF11,AP000873.4 Ensembl:ENSG00000165494,Ensembl:ENSG00000254676 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947403633 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5246098 RMVar_hsa_circ_269664,RMVar_hsa_circ_152142 13611 RMVar_ID_13611 Human_SNP_ID_474606190 A-to-I Human chr11 + 83211743 83211743 83211743 GAGGATTTGGGAGCCCAGGGATTTGAGGCTACAGTGAGCTGTGATTGCACCACTGCACTCCAGTG GAGGATTTGGGAGCCCAGGGATTTGAGGCTACGGTGAGCTGTGATTGCACCACTGCACTCCAGTG A G ANKRD42 Ensembl:ENSG00000137494 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs938942062 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6675,RMVar_hsa_circ_268942,RMVar_hsa_circ_349115,RMVar_hsa_circ_102220,RMVar_hsa_circ_62974,RMVar_hsa_circ_36374,RMVar_hsa_circ_301628,RMVar_hsa_circ_354982,RMVar_hsa_circ_152159,RMVar_hsa_circ_325435,RMVar_hsa_circ_295952,RMVar_hsa_circ_284019,RMVar_hsa_circ_77328,RMVar_hsa_circ_152161,RMVar_hsa_circ_152162,RMVar_hsa_circ_69182,RMVar_hsa_circ_152163 13612 RMVar_ID_13612 Human_SNP_ID_474624446 A-to-I Human chr11 - 83285786 83285786 83285786 CCGTGGGGTCGCGCCTGCTCGAGCGAACGGGAAGAGAAGGTGCCACGCCCTCCTCCCGGATTCAC CCGTGGGGTCGCGCCTGCTCGAGCGAACGGGAGGAGAAGGTGCCACGCCCTCCTCCCGGATTCAC T C CCDC90B Ensembl:ENSG00000137500 Protein coding intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs531714604 Functional Loss SNV dbSNP153 33..33 33 - - - 13613 RMVar_ID_13613 Human_SNP_ID_474629707 A-to-I Human chr11 + 83308466 83308466 83308466 GGCCAGGAGTTTAAGACCAGCCTGGGCAACATAGTGAGACCGTGTGTCTACAGAAAATAAAAAGA GGCCAGGAGTTTAAGACCAGCCTGGGCAACATGGTGAGACCGTGTGTCTACAGAAAATAAAAAGA A G AP000446.1 Ensembl:ENSG00000255234 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs972430799 Functional Loss SNV dbSNP153 33..33 33 - - - 13614 RMVar_ID_13614 Human_SNP_ID_474739021 A-to-I Human chr11 - 83739813 83739813 83739813 CAGCTGCACTGTGATGAGTCCATGAGAATCCAAGGAACTCCATACTGTGGTGTACCCTGAGGTCC CAGCTGCACTGTGATGAGTCCATGAGAATCCACGGAACTCCATACTGTGGTGTACCCTGAGGTCC T G DLG2 Ensembl:ENSG00000150672 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1475408916 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74269,RMVar_hsa_circ_152180,RMVar_hsa_circ_7891,RMVar_hsa_circ_33638,RMVar_hsa_circ_4146 13615 RMVar_ID_13615 Human_SNP_ID_474739043 A-to-I Human chr11 - 83739897 83739897 83739897 CCAGATGCTTGGGCATCATATCCTAATTACCAAGTGTCGTCAAGCCTACTTCCTACATACCTCTC CCAGATGCTTGGGCATCATATCCTAATTACCAGGTGTCGTCAAGCCTACTTCCTACATACCTCTC T C DLG2 Ensembl:ENSG00000150672 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs558965373 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74269,RMVar_hsa_circ_152180,RMVar_hsa_circ_7891,RMVar_hsa_circ_33638,RMVar_hsa_circ_4146 13616 RMVar_ID_13616 Human_SNP_ID_474739044 A-to-I Human chr11 - 83739912 83739912 83739912 AGGTTCTCCATCCACCCAGATGCTTGGGCATCATATCCTAATTACCAAGTGTCGTCAAGCCTACT AGGTTCTCCATCCACCCAGATGCTTGGGCATCGTATCCTAATTACCAAGTGTCGTCAAGCCTACT T C DLG2 Ensembl:ENSG00000150672 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs908754763 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74269,RMVar_hsa_circ_152180,RMVar_hsa_circ_7891,RMVar_hsa_circ_33638,RMVar_hsa_circ_4146 13617 RMVar_ID_13617 Human_SNP_ID_474820120 A-to-I Human chr11 - 84053177 84053177 84053177 TCAGCTGCCACTTGTAAGTGAGAACATGCTGTATCTGGCTTTCTGTTCCTGCATTAGTTTGCTGA TCAGCTGCCACTTGTAAGTGAGAACATGCTGTGTCTGGCTTTCTGTTCCTGCATTAGTTTGCTGA T C DLG2 Ensembl:ENSG00000150672 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs994967133 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4175,RMVar_hsa_circ_7891,RMVar_hsa_circ_338171,RMVar_hsa_circ_12945,RMVar_hsa_circ_61064,RMVar_hsa_circ_152191 13618 RMVar_ID_13618 Human_SNP_ID_475011894 A-to-I Human chr11 - 84775336 84775336 84775336 TCTCCTAACTGCTTTCCACAGTGGCTGGACTAATTTACATTCCCACCAAAGGTGTACAAGCATTC TCTCCTAACTGCTTTCCACAGTGGCTGGACTACTTTACATTCCCACCAAAGGTGTACAAGCATTC T G DLG2 Ensembl:ENSG00000150672 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs989394691 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7891,RMVar_hsa_circ_22698 13619 RMVar_ID_13619 Human_SNP_ID_475012773 A-to-I Human chr11 - 84778019 84778019 84778019 AAAACTCTTCTGGATATCGGTCTAGGCAAAGAATTTATGACTAACTCCTGAAAAGCACAGGCAAC AAAACTCTTCTGGATATCGGTCTAGGCAAAGAGTTTATGACTAACTCCTGAAAAGCACAGGCAAC T C DLG2 Ensembl:ENSG00000150672 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1375288674 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7891,RMVar_hsa_circ_22698 13620 RMVar_ID_13620 Human_SNP_ID_475013202 A-to-I Human chr11 - 84779426 84779426 84779426 AAAAACTCCTAGATTTGATAAGTGAATTTAGTAAAGTTGTAGGATATAAAATCAATGTATAAAAA AAAAACTCCTAGATTTGATAAGTGAATTTAGTGAAGTTGTAGGATATAAAATCAATGTATAAAAA T C DLG2 Ensembl:ENSG00000150672 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1438644494 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7891,RMVar_hsa_circ_22698 13621 RMVar_ID_13621 Human_SNP_ID_475030683 A-to-I Human chr11 - 84840800 84840800 84840800 CTCTGGTGTGTGATGTCCCCGACCTGTGTCCAAGTGTTCTCATTGTTCAATTCCCAGCTATGAGT CTCTGGTGTGTGATGTCCCCGACCTGTGTCCAGGTGTTCTCATTGTTCAATTCCCAGCTATGAGT T C DLG2 Ensembl:ENSG00000150672 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs552926862 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7891,RMVar_hsa_circ_22698 13622 RMVar_ID_13622 Human_SNP_ID_475030684 A-to-I Human chr11 - 84840800 84840800 84840800 CTCTGGTGTGTGATGTCCCCGACCTGTGTCCAAGTGTTCTCATTGTTCAATTCCCAGCTATGAGT CTCTGGTGTGTGATGTCCCCGACCTGTGTCCACGTGTTCTCATTGTTCAATTCCCAGCTATGAGT T G DLG2 Ensembl:ENSG00000150672 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs552926862 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7891,RMVar_hsa_circ_22698 13623 RMVar_ID_13623 Human_SNP_ID_475035811 A-to-I Human chr11 - 84857971 84857971 84857971 GGTGGATAGCTTGAGTCTGGAAAGTCCAGGCTACAGTGAGCATTGACTGAATCACTGCACTCCAG GGTGGATAGCTTGAGTCTGGAAAGTCCAGGCTTCAGTGAGCATTGACTGAATCACTGCACTCCAG T A DLG2 Ensembl:ENSG00000150672 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs986327411 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7891,RMVar_hsa_circ_22698 13624 RMVar_ID_13624 Human_SNP_ID_475250197 A-to-I Human chr11 + 85648017 85648017 85648017 GCCAAAGATGGCTGCGCCCAGGTAATTTGAGCAAAGGCCACAGTGAACTCCGGCGTGGCTGAGGA GCCAAAGATGGCTGCGCCCAGGTAATTTGAGCGAAGGCCACAGTGAACTCCGGCGTGGCTGAGGA A G TMEM126A Ensembl:ENSG00000171202 Protein coding 5'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs901087812 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 13625 RMVar_ID_13625 Human_SNP_ID_475332316 A-to-I Human chr11 - 85971553 85971553 85971553 TTTTGTATTTTTTTTAGAGATGGAGTTTTGCCATGTTGCCCAGGCTGTTCTTGAACTCCTGAGCT TTTTGTATTTTTTTTAGAGATGGAGTTTTGCCGTGTTGCCCAGGCTGTTCTTGAACTCCTGAGCT T C PICALM Ensembl:ENSG00000073921 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1158946693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17560121 RMVar_hsa_circ_152236,RMVar_hsa_circ_290705 13626 RMVar_ID_13626 Human_SNP_ID_475339521 A-to-I Human chr11 - 85997609 85997609 85997609 AAAATTAGCCGGATGCGGTGCTGCGCACCTGTAGTCCCAGCTGCTTGGGAGGCTAAGGCAGGAGA AAAATTAGCCGGATGCGGTGCTGCGCACCTGTCGTCCCAGCTGCTTGGGAGGCTAAGGCAGGAGA T G PICALM Ensembl:ENSG00000073921 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs947699824 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_152257,RMVar_hsa_circ_368290,RMVar_hsa_circ_373209,RMVar_hsa_circ_295279,RMVar_hsa_circ_286180,RMVar_hsa_circ_272337,RMVar_hsa_circ_272743,RMVar_hsa_circ_119740,RMVar_hsa_circ_15803,RMVar_hsa_circ_7852,RMVar_hsa_circ_152240,RMVar_hsa_circ_152241,RMVar_hsa_circ_108911,RMVar_hsa_circ_152238,RMVar_hsa_circ_152239,RMVar_hsa_circ_152237,RMVar_hsa_circ_92742,RMVar_hsa_circ_57042,RMVar_hsa_circ_152251,RMVar_hsa_circ_152252,RMVar_hsa_circ_342236,RMVar_hsa_circ_357005,RMVar_hsa_circ_346191,RMVar_hsa_circ_332531,RMVar_hsa_circ_322833,RMVar_hsa_circ_284486,RMVar_hsa_circ_280441,RMVar_hsa_circ_52067,RMVar_hsa_circ_152259,RMVar_hsa_circ_152260,RMVar_hsa_circ_152258,RMVar_hsa_circ_32368,RMVar_hsa_circ_152269,RMVar_hsa_circ_7129,RMVar_hsa_circ_299460,RMVar_hsa_circ_114749,RMVar_hsa_circ_83938,RMVar_hsa_circ_152270,RMVar_hsa_circ_51418,RMVar_hsa_circ_100199,RMVar_hsa_circ_152268,RMVar_hsa_circ_152280,RMVar_hsa_circ_320251,RMVar_hsa_circ_152278,RMVar_hsa_circ_368945,RMVar_hsa_circ_370213,RMVar_hsa_circ_357923,RMVar_hsa_circ_274205,RMVar_hsa_circ_91665,RMVar_hsa_circ_65207,RMVar_hsa_circ_298472,RMVar_hsa_circ_303125,RMVar_hsa_circ_152279,RMVar_hsa_circ_303012,RMVar_hsa_circ_294372,RMVar_hsa_circ_64875,RMVar_hsa_circ_152284,RMVar_hsa_circ_152288,RMVar_hsa_circ_279395,RMVar_hsa_circ_152281,RMVar_hsa_circ_152282,RMVar_hsa_circ_281534,RMVar_hsa_circ_310150,RMVar_hsa_circ_329871,RMVar_hsa_circ_297237,RMVar_hsa_circ_279738,RMVar_hsa_circ_271167,RMVar_hsa_circ_275317,RMVar_hsa_circ_55198,RMVar_hsa_circ_152286,RMVar_hsa_circ_152287,RMVar_hsa_circ_152285,RMVar_hsa_circ_152283 13627 RMVar_ID_13627 Human_SNP_ID_475339866 A-to-I Human chr11 - 85998772 85998772 85998772 TTCTCTCTCAATCTCTCTCTCTCTTTTGAGACAGTGACTTACTCTGTCACCCAGGCTGGAGTGCA TTCTCTCTCAATCTCTCTCTCTCTTTTGAGACGGTGACTTACTCTGTCACCCAGGCTGGAGTGCA T C PICALM Ensembl:ENSG00000073921 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs913921523 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19701308,Human_RBP_ID_24906450 RMVar_hsa_circ_152257,RMVar_hsa_circ_368290,RMVar_hsa_circ_373209,RMVar_hsa_circ_295279,RMVar_hsa_circ_286180,RMVar_hsa_circ_272337,RMVar_hsa_circ_272743,RMVar_hsa_circ_119740,RMVar_hsa_circ_15803,RMVar_hsa_circ_7852,RMVar_hsa_circ_152240,RMVar_hsa_circ_152241,RMVar_hsa_circ_108911,RMVar_hsa_circ_152238,RMVar_hsa_circ_152239,RMVar_hsa_circ_152237,RMVar_hsa_circ_92742,RMVar_hsa_circ_57042,RMVar_hsa_circ_152251,RMVar_hsa_circ_152252,RMVar_hsa_circ_342236,RMVar_hsa_circ_357005,RMVar_hsa_circ_346191,RMVar_hsa_circ_332531,RMVar_hsa_circ_322833,RMVar_hsa_circ_284486,RMVar_hsa_circ_280441,RMVar_hsa_circ_52067,RMVar_hsa_circ_152259,RMVar_hsa_circ_152260,RMVar_hsa_circ_152258,RMVar_hsa_circ_32368,RMVar_hsa_circ_152269,RMVar_hsa_circ_7129,RMVar_hsa_circ_299460,RMVar_hsa_circ_114749,RMVar_hsa_circ_83938,RMVar_hsa_circ_152270,RMVar_hsa_circ_51418,RMVar_hsa_circ_100199,RMVar_hsa_circ_152268,RMVar_hsa_circ_152280,RMVar_hsa_circ_320251,RMVar_hsa_circ_152278,RMVar_hsa_circ_368945,RMVar_hsa_circ_370213,RMVar_hsa_circ_357923,RMVar_hsa_circ_274205,RMVar_hsa_circ_91665,RMVar_hsa_circ_65207,RMVar_hsa_circ_298472,RMVar_hsa_circ_303125,RMVar_hsa_circ_152279,RMVar_hsa_circ_303012,RMVar_hsa_circ_294372,RMVar_hsa_circ_64875,RMVar_hsa_circ_152284,RMVar_hsa_circ_152288,RMVar_hsa_circ_279395,RMVar_hsa_circ_152281,RMVar_hsa_circ_152282,RMVar_hsa_circ_281534,RMVar_hsa_circ_310150,RMVar_hsa_circ_329871,RMVar_hsa_circ_297237,RMVar_hsa_circ_279738,RMVar_hsa_circ_271167,RMVar_hsa_circ_275317,RMVar_hsa_circ_55198,RMVar_hsa_circ_152286,RMVar_hsa_circ_152287,RMVar_hsa_circ_152285,RMVar_hsa_circ_152283 13628 RMVar_ID_13628 Human_SNP_ID_475339904 A-to-I Human chr11 - 85998883 85998883 85998883 GTGGTGGCGTGTGCCTGTTGTCCCAGCTACTCAGGAGGTTGAGGCAGGAGGAAGGCCTGAGCCCA GTGGTGGCGTGTGCCTGTTGTCCCAGCTACTCGGGAGGTTGAGGCAGGAGGAAGGCCTGAGCCCA T C PICALM Ensembl:ENSG00000073921 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs540506285 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_152257,RMVar_hsa_circ_368290,RMVar_hsa_circ_373209,RMVar_hsa_circ_295279,RMVar_hsa_circ_286180,RMVar_hsa_circ_272337,RMVar_hsa_circ_272743,RMVar_hsa_circ_119740,RMVar_hsa_circ_15803,RMVar_hsa_circ_7852,RMVar_hsa_circ_152240,RMVar_hsa_circ_152241,RMVar_hsa_circ_108911,RMVar_hsa_circ_152238,RMVar_hsa_circ_152239,RMVar_hsa_circ_152237,RMVar_hsa_circ_92742,RMVar_hsa_circ_57042,RMVar_hsa_circ_152251,RMVar_hsa_circ_152252,RMVar_hsa_circ_342236,RMVar_hsa_circ_357005,RMVar_hsa_circ_346191,RMVar_hsa_circ_332531,RMVar_hsa_circ_322833,RMVar_hsa_circ_284486,RMVar_hsa_circ_280441,RMVar_hsa_circ_52067,RMVar_hsa_circ_152259,RMVar_hsa_circ_152260,RMVar_hsa_circ_152258,RMVar_hsa_circ_32368,RMVar_hsa_circ_152269,RMVar_hsa_circ_7129,RMVar_hsa_circ_299460,RMVar_hsa_circ_114749,RMVar_hsa_circ_83938,RMVar_hsa_circ_152270,RMVar_hsa_circ_51418,RMVar_hsa_circ_100199,RMVar_hsa_circ_152268,RMVar_hsa_circ_152280,RMVar_hsa_circ_320251,RMVar_hsa_circ_152278,RMVar_hsa_circ_368945,RMVar_hsa_circ_370213,RMVar_hsa_circ_357923,RMVar_hsa_circ_274205,RMVar_hsa_circ_91665,RMVar_hsa_circ_65207,RMVar_hsa_circ_298472,RMVar_hsa_circ_303125,RMVar_hsa_circ_152279,RMVar_hsa_circ_303012,RMVar_hsa_circ_294372,RMVar_hsa_circ_64875,RMVar_hsa_circ_152284,RMVar_hsa_circ_152288,RMVar_hsa_circ_279395,RMVar_hsa_circ_152281,RMVar_hsa_circ_152282,RMVar_hsa_circ_281534,RMVar_hsa_circ_310150,RMVar_hsa_circ_329871,RMVar_hsa_circ_297237,RMVar_hsa_circ_279738,RMVar_hsa_circ_271167,RMVar_hsa_circ_275317,RMVar_hsa_circ_55198,RMVar_hsa_circ_152286,RMVar_hsa_circ_152287,RMVar_hsa_circ_152285,RMVar_hsa_circ_152283 13629 RMVar_ID_13629 Human_SNP_ID_475342365 A-to-I Human chr11 - 86008457 86008457 86008457 TGCCACCATGCCCGGCTAATTTTTGTATTTTTAGTAGAGCTGGGGTTTCACTGTGTTAGCCAGGA TGCCACCATGCCCGGCTAATTTTTGTATTTTTGGTAGAGCTGGGGTTTCACTGTGTTAGCCAGGA T C PICALM Ensembl:ENSG00000073921 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1471891002 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_152257,RMVar_hsa_circ_295279,RMVar_hsa_circ_272337,RMVar_hsa_circ_272743,RMVar_hsa_circ_119740,RMVar_hsa_circ_15803,RMVar_hsa_circ_7852,RMVar_hsa_circ_152238,RMVar_hsa_circ_152237,RMVar_hsa_circ_57042,RMVar_hsa_circ_342236,RMVar_hsa_circ_332531,RMVar_hsa_circ_322833,RMVar_hsa_circ_284486,RMVar_hsa_circ_152258,RMVar_hsa_circ_1706,RMVar_hsa_circ_32368,RMVar_hsa_circ_152269,RMVar_hsa_circ_7129,RMVar_hsa_circ_299460,RMVar_hsa_circ_114749,RMVar_hsa_circ_51418,RMVar_hsa_circ_100199,RMVar_hsa_circ_152268,RMVar_hsa_circ_152280,RMVar_hsa_circ_320251,RMVar_hsa_circ_152278,RMVar_hsa_circ_370213,RMVar_hsa_circ_274205,RMVar_hsa_circ_65207,RMVar_hsa_circ_303012,RMVar_hsa_circ_294372,RMVar_hsa_circ_64875,RMVar_hsa_circ_152288,RMVar_hsa_circ_279395,RMVar_hsa_circ_310150,RMVar_hsa_circ_329871,RMVar_hsa_circ_297237,RMVar_hsa_circ_279738,RMVar_hsa_circ_55198,RMVar_hsa_circ_152286,RMVar_hsa_circ_152287,RMVar_hsa_circ_339157,RMVar_hsa_circ_121530,RMVar_hsa_circ_273929,RMVar_hsa_circ_85100,RMVar_hsa_circ_152295,RMVar_hsa_circ_370518,RMVar_hsa_circ_152290,RMVar_hsa_circ_152289,RMVar_hsa_circ_304884,RMVar_hsa_circ_360237,RMVar_hsa_circ_152296,RMVar_hsa_circ_298649,RMVar_hsa_circ_346370,RMVar_hsa_circ_374123,RMVar_hsa_circ_302447,RMVar_hsa_circ_273802,RMVar_hsa_circ_19046,RMVar_hsa_circ_152298,RMVar_hsa_circ_152299,RMVar_hsa_circ_288067,RMVar_hsa_circ_152297,RMVar_hsa_circ_337054,RMVar_hsa_circ_272959,RMVar_hsa_circ_152300 13630 RMVar_ID_13630 Human_SNP_ID_475342374 A-to-I Human chr11 - 86008485 86008485 86008485 CTGCTGAGTAGCTGGGATTACAGGTGCCTGCCACCATGCCCGGCTAATTTTTGTATTTTTAGTAG CTGCTGAGTAGCTGGGATTACAGGTGCCTGCCGCCATGCCCGGCTAATTTTTGTATTTTTAGTAG T C PICALM Ensembl:ENSG00000073921 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs956374516 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_152257,RMVar_hsa_circ_295279,RMVar_hsa_circ_272337,RMVar_hsa_circ_272743,RMVar_hsa_circ_119740,RMVar_hsa_circ_15803,RMVar_hsa_circ_7852,RMVar_hsa_circ_152238,RMVar_hsa_circ_152237,RMVar_hsa_circ_57042,RMVar_hsa_circ_342236,RMVar_hsa_circ_332531,RMVar_hsa_circ_322833,RMVar_hsa_circ_284486,RMVar_hsa_circ_152258,RMVar_hsa_circ_1706,RMVar_hsa_circ_32368,RMVar_hsa_circ_152269,RMVar_hsa_circ_7129,RMVar_hsa_circ_299460,RMVar_hsa_circ_114749,RMVar_hsa_circ_51418,RMVar_hsa_circ_100199,RMVar_hsa_circ_152268,RMVar_hsa_circ_152280,RMVar_hsa_circ_320251,RMVar_hsa_circ_152278,RMVar_hsa_circ_370213,RMVar_hsa_circ_274205,RMVar_hsa_circ_65207,RMVar_hsa_circ_303012,RMVar_hsa_circ_294372,RMVar_hsa_circ_64875,RMVar_hsa_circ_152288,RMVar_hsa_circ_279395,RMVar_hsa_circ_310150,RMVar_hsa_circ_329871,RMVar_hsa_circ_297237,RMVar_hsa_circ_279738,RMVar_hsa_circ_55198,RMVar_hsa_circ_152286,RMVar_hsa_circ_152287,RMVar_hsa_circ_339157,RMVar_hsa_circ_121530,RMVar_hsa_circ_273929,RMVar_hsa_circ_85100,RMVar_hsa_circ_152295,RMVar_hsa_circ_370518,RMVar_hsa_circ_152290,RMVar_hsa_circ_152289,RMVar_hsa_circ_304884,RMVar_hsa_circ_360237,RMVar_hsa_circ_152296,RMVar_hsa_circ_298649,RMVar_hsa_circ_346370,RMVar_hsa_circ_374123,RMVar_hsa_circ_302447,RMVar_hsa_circ_273802,RMVar_hsa_circ_19046,RMVar_hsa_circ_152298,RMVar_hsa_circ_152299,RMVar_hsa_circ_288067,RMVar_hsa_circ_152297,RMVar_hsa_circ_337054,RMVar_hsa_circ_272959,RMVar_hsa_circ_152300 13631 RMVar_ID_13631 Human_SNP_ID_475342378 A-to-I Human chr11 - 86008496 86008496 86008496 CCTGCTTCAGCCTGCTGAGTAGCTGGGATTACAGGTGCCTGCCACCATGCCCGGCTAATTTTTGT CCTGCTTCAGCCTGCTGAGTAGCTGGGATTACGGGTGCCTGCCACCATGCCCGGCTAATTTTTGT T C PICALM Ensembl:ENSG00000073921 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs146566176 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_152257,RMVar_hsa_circ_295279,RMVar_hsa_circ_272337,RMVar_hsa_circ_272743,RMVar_hsa_circ_119740,RMVar_hsa_circ_15803,RMVar_hsa_circ_7852,RMVar_hsa_circ_152238,RMVar_hsa_circ_152237,RMVar_hsa_circ_57042,RMVar_hsa_circ_342236,RMVar_hsa_circ_332531,RMVar_hsa_circ_322833,RMVar_hsa_circ_284486,RMVar_hsa_circ_152258,RMVar_hsa_circ_1706,RMVar_hsa_circ_32368,RMVar_hsa_circ_152269,RMVar_hsa_circ_7129,RMVar_hsa_circ_299460,RMVar_hsa_circ_114749,RMVar_hsa_circ_51418,RMVar_hsa_circ_100199,RMVar_hsa_circ_152268,RMVar_hsa_circ_152280,RMVar_hsa_circ_320251,RMVar_hsa_circ_152278,RMVar_hsa_circ_370213,RMVar_hsa_circ_274205,RMVar_hsa_circ_65207,RMVar_hsa_circ_303012,RMVar_hsa_circ_294372,RMVar_hsa_circ_64875,RMVar_hsa_circ_152288,RMVar_hsa_circ_279395,RMVar_hsa_circ_310150,RMVar_hsa_circ_329871,RMVar_hsa_circ_297237,RMVar_hsa_circ_279738,RMVar_hsa_circ_55198,RMVar_hsa_circ_152286,RMVar_hsa_circ_152287,RMVar_hsa_circ_339157,RMVar_hsa_circ_121530,RMVar_hsa_circ_273929,RMVar_hsa_circ_85100,RMVar_hsa_circ_152295,RMVar_hsa_circ_370518,RMVar_hsa_circ_152290,RMVar_hsa_circ_152289,RMVar_hsa_circ_304884,RMVar_hsa_circ_360237,RMVar_hsa_circ_152296,RMVar_hsa_circ_298649,RMVar_hsa_circ_346370,RMVar_hsa_circ_374123,RMVar_hsa_circ_302447,RMVar_hsa_circ_273802,RMVar_hsa_circ_19046,RMVar_hsa_circ_152298,RMVar_hsa_circ_152299,RMVar_hsa_circ_288067,RMVar_hsa_circ_152297,RMVar_hsa_circ_337054,RMVar_hsa_circ_272959,RMVar_hsa_circ_152300 13632 RMVar_ID_13632 Human_SNP_ID_475342380 A-to-I Human chr11 - 86008508 86008508 86008508 TCAAACGATTCTCCTGCTTCAGCCTGCTGAGTAGCTGGGATTACAGGTGCCTGCCACCATGCCCG TCAAACGATTCTCCTGCTTCAGCCTGCTGAGTTGCTGGGATTACAGGTGCCTGCCACCATGCCCG T A PICALM Ensembl:ENSG00000073921 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1436966743 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_152257,RMVar_hsa_circ_295279,RMVar_hsa_circ_272337,RMVar_hsa_circ_272743,RMVar_hsa_circ_119740,RMVar_hsa_circ_15803,RMVar_hsa_circ_7852,RMVar_hsa_circ_152238,RMVar_hsa_circ_152237,RMVar_hsa_circ_57042,RMVar_hsa_circ_342236,RMVar_hsa_circ_332531,RMVar_hsa_circ_322833,RMVar_hsa_circ_284486,RMVar_hsa_circ_152258,RMVar_hsa_circ_1706,RMVar_hsa_circ_32368,RMVar_hsa_circ_152269,RMVar_hsa_circ_7129,RMVar_hsa_circ_299460,RMVar_hsa_circ_114749,RMVar_hsa_circ_51418,RMVar_hsa_circ_100199,RMVar_hsa_circ_152268,RMVar_hsa_circ_152280,RMVar_hsa_circ_320251,RMVar_hsa_circ_152278,RMVar_hsa_circ_370213,RMVar_hsa_circ_274205,RMVar_hsa_circ_65207,RMVar_hsa_circ_303012,RMVar_hsa_circ_294372,RMVar_hsa_circ_64875,RMVar_hsa_circ_152288,RMVar_hsa_circ_279395,RMVar_hsa_circ_310150,RMVar_hsa_circ_329871,RMVar_hsa_circ_297237,RMVar_hsa_circ_279738,RMVar_hsa_circ_55198,RMVar_hsa_circ_152286,RMVar_hsa_circ_152287,RMVar_hsa_circ_339157,RMVar_hsa_circ_121530,RMVar_hsa_circ_273929,RMVar_hsa_circ_85100,RMVar_hsa_circ_152295,RMVar_hsa_circ_370518,RMVar_hsa_circ_152290,RMVar_hsa_circ_152289,RMVar_hsa_circ_304884,RMVar_hsa_circ_360237,RMVar_hsa_circ_152296,RMVar_hsa_circ_298649,RMVar_hsa_circ_346370,RMVar_hsa_circ_374123,RMVar_hsa_circ_302447,RMVar_hsa_circ_273802,RMVar_hsa_circ_19046,RMVar_hsa_circ_152298,RMVar_hsa_circ_152299,RMVar_hsa_circ_288067,RMVar_hsa_circ_152297,RMVar_hsa_circ_337054,RMVar_hsa_circ_272959,RMVar_hsa_circ_152300 13633 RMVar_ID_13633 Human_SNP_ID_475342394 A-to-I Human chr11 - 86008537 86008537 86008537 CTGCTCACTGCACCCTCTACCTCCCGGGTTCAAACGATTCTCCTGCTTCAGCCTGCTGAGTAGCT CTGCTCACTGCACCCTCTACCTCCCGGGTTCAGACGATTCTCCTGCTTCAGCCTGCTGAGTAGCT T C PICALM Ensembl:ENSG00000073921 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs80056942 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11734585 RMVar_hsa_circ_152257,RMVar_hsa_circ_295279,RMVar_hsa_circ_272337,RMVar_hsa_circ_272743,RMVar_hsa_circ_119740,RMVar_hsa_circ_15803,RMVar_hsa_circ_7852,RMVar_hsa_circ_152238,RMVar_hsa_circ_152237,RMVar_hsa_circ_57042,RMVar_hsa_circ_342236,RMVar_hsa_circ_332531,RMVar_hsa_circ_322833,RMVar_hsa_circ_284486,RMVar_hsa_circ_152258,RMVar_hsa_circ_1706,RMVar_hsa_circ_32368,RMVar_hsa_circ_152269,RMVar_hsa_circ_7129,RMVar_hsa_circ_299460,RMVar_hsa_circ_114749,RMVar_hsa_circ_51418,RMVar_hsa_circ_100199,RMVar_hsa_circ_152268,RMVar_hsa_circ_152280,RMVar_hsa_circ_320251,RMVar_hsa_circ_152278,RMVar_hsa_circ_370213,RMVar_hsa_circ_274205,RMVar_hsa_circ_65207,RMVar_hsa_circ_303012,RMVar_hsa_circ_294372,RMVar_hsa_circ_64875,RMVar_hsa_circ_152288,RMVar_hsa_circ_279395,RMVar_hsa_circ_310150,RMVar_hsa_circ_329871,RMVar_hsa_circ_297237,RMVar_hsa_circ_279738,RMVar_hsa_circ_55198,RMVar_hsa_circ_152286,RMVar_hsa_circ_152287,RMVar_hsa_circ_339157,RMVar_hsa_circ_121530,RMVar_hsa_circ_273929,RMVar_hsa_circ_85100,RMVar_hsa_circ_152295,RMVar_hsa_circ_370518,RMVar_hsa_circ_152290,RMVar_hsa_circ_152289,RMVar_hsa_circ_304884,RMVar_hsa_circ_360237,RMVar_hsa_circ_152296,RMVar_hsa_circ_298649,RMVar_hsa_circ_346370,RMVar_hsa_circ_374123,RMVar_hsa_circ_302447,RMVar_hsa_circ_273802,RMVar_hsa_circ_19046,RMVar_hsa_circ_152298,RMVar_hsa_circ_152299,RMVar_hsa_circ_288067,RMVar_hsa_circ_152297,RMVar_hsa_circ_337054,RMVar_hsa_circ_272959,RMVar_hsa_circ_152300 13634 RMVar_ID_13634 Human_SNP_ID_475342629 A-to-I Human chr11 - 86009169 86009169 86009169 CCTGCCTCAGCTTCCTGGGTAGCTGGGATTACAGGTGCCCGCCACCACGCCCAGCTAATTTTAGA CCTGCCTCAGCTTCCTGGGTAGCTGGGATTACGGGTGCCCGCCACCACGCCCAGCTAATTTTAGA T C PICALM Ensembl:ENSG00000073921 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs975097205 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_152257,RMVar_hsa_circ_295279,RMVar_hsa_circ_272337,RMVar_hsa_circ_272743,RMVar_hsa_circ_119740,RMVar_hsa_circ_15803,RMVar_hsa_circ_7852,RMVar_hsa_circ_152238,RMVar_hsa_circ_152237,RMVar_hsa_circ_57042,RMVar_hsa_circ_342236,RMVar_hsa_circ_332531,RMVar_hsa_circ_322833,RMVar_hsa_circ_284486,RMVar_hsa_circ_152258,RMVar_hsa_circ_1706,RMVar_hsa_circ_32368,RMVar_hsa_circ_152269,RMVar_hsa_circ_7129,RMVar_hsa_circ_299460,RMVar_hsa_circ_114749,RMVar_hsa_circ_51418,RMVar_hsa_circ_100199,RMVar_hsa_circ_152268,RMVar_hsa_circ_152280,RMVar_hsa_circ_320251,RMVar_hsa_circ_152278,RMVar_hsa_circ_370213,RMVar_hsa_circ_274205,RMVar_hsa_circ_65207,RMVar_hsa_circ_303012,RMVar_hsa_circ_294372,RMVar_hsa_circ_64875,RMVar_hsa_circ_152288,RMVar_hsa_circ_279395,RMVar_hsa_circ_310150,RMVar_hsa_circ_329871,RMVar_hsa_circ_297237,RMVar_hsa_circ_279738,RMVar_hsa_circ_55198,RMVar_hsa_circ_152286,RMVar_hsa_circ_152287,RMVar_hsa_circ_339157,RMVar_hsa_circ_121530,RMVar_hsa_circ_273929,RMVar_hsa_circ_85100,RMVar_hsa_circ_152295,RMVar_hsa_circ_370518,RMVar_hsa_circ_152290,RMVar_hsa_circ_152289,RMVar_hsa_circ_304884,RMVar_hsa_circ_360237,RMVar_hsa_circ_152296,RMVar_hsa_circ_298649,RMVar_hsa_circ_346370,RMVar_hsa_circ_374123,RMVar_hsa_circ_302447,RMVar_hsa_circ_273802,RMVar_hsa_circ_19046,RMVar_hsa_circ_152298,RMVar_hsa_circ_152299,RMVar_hsa_circ_288067,RMVar_hsa_circ_152297,RMVar_hsa_circ_337054,RMVar_hsa_circ_272959,RMVar_hsa_circ_152300 13635 RMVar_ID_13635 Human_SNP_ID_475342818 A-to-I Human chr11 - 86009609 86009609 86009609 TGGCTCACTGCAACCTCCACCTCCTGGGTTCAAGCGATTCTGCTGTCTCAGCCTCCCGAGTAGCT TGGCTCACTGCAACCTCCACCTCCTGGGTTCAGGCGATTCTGCTGTCTCAGCCTCCCGAGTAGCT T C PICALM Ensembl:ENSG00000073921 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1338343736 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_152257,RMVar_hsa_circ_295279,RMVar_hsa_circ_272337,RMVar_hsa_circ_272743,RMVar_hsa_circ_119740,RMVar_hsa_circ_15803,RMVar_hsa_circ_7852,RMVar_hsa_circ_152238,RMVar_hsa_circ_152237,RMVar_hsa_circ_57042,RMVar_hsa_circ_342236,RMVar_hsa_circ_332531,RMVar_hsa_circ_322833,RMVar_hsa_circ_284486,RMVar_hsa_circ_152258,RMVar_hsa_circ_1706,RMVar_hsa_circ_32368,RMVar_hsa_circ_152269,RMVar_hsa_circ_7129,RMVar_hsa_circ_299460,RMVar_hsa_circ_114749,RMVar_hsa_circ_51418,RMVar_hsa_circ_100199,RMVar_hsa_circ_152268,RMVar_hsa_circ_152280,RMVar_hsa_circ_320251,RMVar_hsa_circ_152278,RMVar_hsa_circ_370213,RMVar_hsa_circ_274205,RMVar_hsa_circ_65207,RMVar_hsa_circ_303012,RMVar_hsa_circ_294372,RMVar_hsa_circ_64875,RMVar_hsa_circ_152288,RMVar_hsa_circ_279395,RMVar_hsa_circ_310150,RMVar_hsa_circ_329871,RMVar_hsa_circ_297237,RMVar_hsa_circ_279738,RMVar_hsa_circ_55198,RMVar_hsa_circ_152286,RMVar_hsa_circ_152287,RMVar_hsa_circ_339157,RMVar_hsa_circ_121530,RMVar_hsa_circ_273929,RMVar_hsa_circ_85100,RMVar_hsa_circ_152295,RMVar_hsa_circ_370518,RMVar_hsa_circ_152290,RMVar_hsa_circ_152289,RMVar_hsa_circ_304884,RMVar_hsa_circ_360237,RMVar_hsa_circ_152296,RMVar_hsa_circ_298649,RMVar_hsa_circ_346370,RMVar_hsa_circ_374123,RMVar_hsa_circ_302447,RMVar_hsa_circ_273802,RMVar_hsa_circ_19046,RMVar_hsa_circ_152298,RMVar_hsa_circ_152299,RMVar_hsa_circ_288067,RMVar_hsa_circ_152297,RMVar_hsa_circ_337054,RMVar_hsa_circ_272959,RMVar_hsa_circ_152300 13636 RMVar_ID_13636 Human_SNP_ID_475343042 A-to-I Human chr11 - 86010506 86010506 86010506 ACTGGCCAACATGGCAAAATCCCGTCTATACTAAAGATACAAAAATTAGCCAGTCATGGAGGCGG ACTGGCCAACATGGCAAAATCCCGTCTATACTGAAGATACAAAAATTAGCCAGTCATGGAGGCGG T C PICALM Ensembl:ENSG00000073921 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1565399084 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_152257,RMVar_hsa_circ_295279,RMVar_hsa_circ_272337,RMVar_hsa_circ_272743,RMVar_hsa_circ_119740,RMVar_hsa_circ_15803,RMVar_hsa_circ_7852,RMVar_hsa_circ_152238,RMVar_hsa_circ_152237,RMVar_hsa_circ_57042,RMVar_hsa_circ_342236,RMVar_hsa_circ_332531,RMVar_hsa_circ_322833,RMVar_hsa_circ_284486,RMVar_hsa_circ_152258,RMVar_hsa_circ_1706,RMVar_hsa_circ_32368,RMVar_hsa_circ_152269,RMVar_hsa_circ_7129,RMVar_hsa_circ_299460,RMVar_hsa_circ_114749,RMVar_hsa_circ_51418,RMVar_hsa_circ_100199,RMVar_hsa_circ_152268,RMVar_hsa_circ_152280,RMVar_hsa_circ_320251,RMVar_hsa_circ_152278,RMVar_hsa_circ_370213,RMVar_hsa_circ_274205,RMVar_hsa_circ_65207,RMVar_hsa_circ_303012,RMVar_hsa_circ_294372,RMVar_hsa_circ_64875,RMVar_hsa_circ_152288,RMVar_hsa_circ_279395,RMVar_hsa_circ_310150,RMVar_hsa_circ_329871,RMVar_hsa_circ_297237,RMVar_hsa_circ_279738,RMVar_hsa_circ_55198,RMVar_hsa_circ_152286,RMVar_hsa_circ_152287,RMVar_hsa_circ_339157,RMVar_hsa_circ_121530,RMVar_hsa_circ_273929,RMVar_hsa_circ_85100,RMVar_hsa_circ_152295,RMVar_hsa_circ_370518,RMVar_hsa_circ_152290,RMVar_hsa_circ_152289,RMVar_hsa_circ_304884,RMVar_hsa_circ_360237,RMVar_hsa_circ_152296,RMVar_hsa_circ_298649,RMVar_hsa_circ_346370,RMVar_hsa_circ_374123,RMVar_hsa_circ_302447,RMVar_hsa_circ_273802,RMVar_hsa_circ_19046,RMVar_hsa_circ_152298,RMVar_hsa_circ_152299,RMVar_hsa_circ_288067,RMVar_hsa_circ_152297,RMVar_hsa_circ_337054,RMVar_hsa_circ_272959,RMVar_hsa_circ_152300 13637 RMVar_ID_13637 Human_SNP_ID_475392427 A-to-I Human chr11 - 86195888 86195888 86195888 AGTGTATTGGACTTCTCTCTCCAATACAGCACAATCATTGTAGCCAGTGGTGTTGGAAATAACAA AGTGTATTGGACTTCTCTCTCCAATACAGCACGATCATTGTAGCCAGTGGTGTTGGAAATAACAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs907562285 Functional Loss SNV dbSNP153 33..33 33 - - - 13638 RMVar_ID_13638 Human_SNP_ID_475392428 A-to-I Human chr11 - 86195888 86195888 86195888 AGTGTATTGGACTTCTCTCTCCAATACAGCACAATCATTGTAGCCAGTGGTGTTGGAAATAACAA AGTGTATTGGACTTCTCTCTCCAATACAGCACCATCATTGTAGCCAGTGGTGTTGGAAATAACAA T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs907562285 Functional Loss SNV dbSNP153 33..33 33 - - - 13639 RMVar_ID_13639 Human_SNP_ID_475415083 A-to-I Human chr11 + 86285620 86285619 86285621 ATTGTGTAATGATCATTTTATTTTTTTGAGACAGAGTTTCGCTCTTGTTGCCCGGGCTGGAGTGC ATTGTGTAATGATCATTTTATTTTTTTGAGAC__AGTTTCGCTCTTGTTGCCCGGGCTGGAGTGC CAG C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs755312778 Functional Loss DEL dbSNP153 33..34 33 - - - 13640 RMVar_ID_13640 Human_SNP_ID_475415149 A-to-I Human chr11 + 86285851 86285851 86285851 AACTCCTGACCTCAAGTGATCCAACCTGCCTCAGCCTCCCAAGGTGCTGGGATTACAGGTGTGAG AACTCCTGACCTCAAGTGATCCAACCTGCCTCGGCCTCCCAAGGTGCTGGGATTACAGGTGTGAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs974083149 Functional Loss SNV dbSNP153 33..33 33 - - - 13641 RMVar_ID_13641 Human_SNP_ID_475423710 A-to-I Human chr11 + 86316999 86316999 86316999 TATTTTTAGTAGAGGCAGGGTTCCACCTTGTTAGCCAGGATGGTCTCGATCTCCTGACCTTGTGA TATTTTTAGTAGAGGCAGGGTTCCACCTTGTTGGCCAGGATGGTCTCGATCTCCTGACCTTGTGA A G HIKESHI Ensembl:ENSG00000149196 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs888365900 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91379,RMVar_hsa_circ_152322,RMVar_hsa_circ_152324,RMVar_hsa_circ_307320 13642 RMVar_ID_13642 Human_SNP_ID_475424802 A-to-I Human chr11 + 86320411 86320411 86320411 ACCAGCCTGGCTAACGTGGTGAAACCCTGTCTACTAAAAACACAAAAATTAGCTGGGCGTGCTGG ACCAGCCTGGCTAACGTGGTGAAACCCTGTCTGCTAAAAACACAAAAATTAGCTGGGCGTGCTGG A G HIKESHI Ensembl:ENSG00000149196 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1565729989 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91379,RMVar_hsa_circ_152322,RMVar_hsa_circ_152324,RMVar_hsa_circ_307320 13643 RMVar_ID_13643 Human_SNP_ID_475426415 A-to-I Human chr11 + 86326970 86326970 86326970 TTTTAGAGCTGGGCATGGTGGCGTGTGCCTATAGTCCTAACTACTCGGGAGGCTGAAGTGGGAGG TTTTAGAGCTGGGCATGGTGGCGTGTGCCTATGGTCCTAACTACTCGGGAGGCTGAAGTGGGAGG A G HIKESHI Ensembl:ENSG00000149196 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904840463 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91379,RMVar_hsa_circ_152322,RMVar_hsa_circ_355812 13644 RMVar_ID_13644 Human_SNP_ID_475430505 A-to-I Human chr11 + 86343453 86343453 86343453 GCCTAGAATTTTGAGACCAGCCTGGGTAACATAGTGAGACCCTGTCTTTATAAAAAGATAAAAAA GCCTAGAATTTTGAGACCAGCCTGGGTAACATGGTGAGACCCTGTCTTTATAAAAAGATAAAAAA A G HIKESHI Ensembl:ENSG00000149196 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432552372 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23525202 13645 RMVar_ID_13645 Human_SNP_ID_475430538 A-to-I Human chr11 + 86343616 86343616 86343616 ATGATTGTGCCACTGCATTCCAGCCTGGGTGAAAGAGTGGGACCCTGTCTCAAAAACAAACGAAG ATGATTGTGCCACTGCATTCCAGCCTGGGTGAGAGAGTGGGACCCTGTCTCAAAAACAAACGAAG A G HIKESHI Ensembl:ENSG00000149196 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs919471148 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11738083 13646 RMVar_ID_13646 Human_SNP_ID_475430690 A-to-I Human chr11 + 86344402 86344402 86344402 GTTGCACAGGCTGGTCTTGAATGCCTGGCCTCAAGTGATTCTCCTGCCTCAGCCTCCCAAAGTTT GTTGCACAGGCTGGTCTTGAATGCCTGGCCTCCAGTGATTCTCCTGCCTCAGCCTCCCAAAGTTT A C HIKESHI Ensembl:ENSG00000149196 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1453797435 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11738105 13647 RMVar_ID_13647 Human_SNP_ID_475517187 A-to-I Human chr11 + 86686288 86686279 86686289 ACACGTATATGTACGTATATACACATATACGTATATATACGTATATATACATGCTTGTGTATATA ACACGTATATGTACGTATATACAC__________ATATACGTATATATACATGCTTGTGTATATA CATATACGTAT C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1180736524 Functional Loss DEL dbSNP153 25..34 33 - - - 13648 RMVar_ID_13648 Human_SNP_ID_475620510 A-to-I Human chr11 + 87089266 87089266 87089266 ACCTTGAAATGCATTTGTCAGCGGGGTACGGTAGCACATGCCTGTAATCCCAGAACTTTGGGGTG ACCTTGAAATGCATTTGTCAGCGGGGTACGGTGGCACATGCCTGTAATCCCAGAACTTTGGGGTG A G TMEM135 Ensembl:ENSG00000166575 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1469605290 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3556,RMVar_hsa_circ_152351,RMVar_hsa_circ_118114,RMVar_hsa_circ_289290,RMVar_hsa_circ_340535,RMVar_hsa_circ_296868,RMVar_hsa_circ_112557,RMVar_hsa_circ_152355,RMVar_hsa_circ_152356,RMVar_hsa_circ_152357,RMVar_hsa_circ_326751,RMVar_hsa_circ_152358,RMVar_hsa_circ_152359 13649 RMVar_ID_13649 Human_SNP_ID_475635546 A-to-I Human chr11 + 87147897 87147897 87147897 CTCCTGCCTCAGCCTCCCGAGTAGCCAGGACTACAGGCACGCACCACCATGCCTAGCTAATTTTC CTCCTGCCTCAGCCTCCCGAGTAGCCAGGACTGCAGGCACGCACCACCATGCCTAGCTAATTTTC A G TMEM135 Ensembl:ENSG00000166575 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1029365736 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3556,RMVar_hsa_circ_152351,RMVar_hsa_circ_118114,RMVar_hsa_circ_340535,RMVar_hsa_circ_296868,RMVar_hsa_circ_112557,RMVar_hsa_circ_152357,RMVar_hsa_circ_326751,RMVar_hsa_circ_152359,RMVar_hsa_circ_152360,RMVar_hsa_circ_76096,RMVar_hsa_circ_348371 13650 RMVar_ID_13650 Human_SNP_ID_475653100 A-to-I Human chr11 + 87214705 87214705 87214705 TTTAAAGCTTTTTCCCCCTATATTACATCACTACAGAATGTTATGGGAAGGAAAAACTGAAGCTA TTTAAAGCTTTTTCCCCCTATATTACATCACTGCAGAATGTTATGGGAAGGAAAAACTGAAGCTA A G TMEM135 Ensembl:ENSG00000166575 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167863128 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3556,RMVar_hsa_circ_152351,RMVar_hsa_circ_118114,RMVar_hsa_circ_340535,RMVar_hsa_circ_112557,RMVar_hsa_circ_73517,RMVar_hsa_circ_152359,RMVar_hsa_circ_152360,RMVar_hsa_circ_76096,RMVar_hsa_circ_318128,RMVar_hsa_circ_337744 13651 RMVar_ID_13651 Human_SNP_ID_475655908 A-to-I Human chr11 + 87225546 87225546 87225546 TATCATTAAAAATGCAATTCAAAATAAACAAGAAAAGAATTAATGTGGACAGGAAGAGTGAGGAA TATCATTAAAAATGCAATTCAAAATAAACAAGGAAAGAATTAATGTGGACAGGAAGAGTGAGGAA A G TMEM135 Ensembl:ENSG00000166575 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1478999379 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3556,RMVar_hsa_circ_152351,RMVar_hsa_circ_118114,RMVar_hsa_circ_340535,RMVar_hsa_circ_112557,RMVar_hsa_circ_73517,RMVar_hsa_circ_152359,RMVar_hsa_circ_152360,RMVar_hsa_circ_76096,RMVar_hsa_circ_318128,RMVar_hsa_circ_337744 13652 RMVar_ID_13652 Human_SNP_ID_475955216 A-to-I Human chr11 - 88322381 88322381 88322381 TCAACTTACGATGGATTAAAGACTTAAATGTAAAACCCAAAATTATAAAACCCTGGAATAGAATA TCAACTTACGATGGATTAAAGACTTAAATGTAGAACCCAAAATTATAAAACCCTGGAATAGAATA T C CTSC Ensembl:ENSG00000109861 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900287783 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26408906 13653 RMVar_ID_13653 Human_SNP_ID_475955217 A-to-I Human chr11 - 88322381 88322381 88322381 TCAACTTACGATGGATTAAAGACTTAAATGTAAAACCCAAAATTATAAAACCCTGGAATAGAATA TCAACTTACGATGGATTAAAGACTTAAATGTACAACCCAAAATTATAAAACCCTGGAATAGAATA T G CTSC Ensembl:ENSG00000109861 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900287783 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26408906 13654 RMVar_ID_13654 Human_SNP_ID_475955221 A-to-I Human chr11 - 88322395 88322395 88322395 TCCATATACGAAAATCAACTTACGATGGATTAAAGACTTAAATGTAAAACCCAAAATTATAAAAC TCCATATACGAAAATCAACTTACGATGGATTAGAGACTTAAATGTAAAACCCAAAATTATAAAAC T C CTSC Ensembl:ENSG00000109861 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170239478 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26408906 13655 RMVar_ID_13655 Human_SNP_ID_475955227 A-to-I Human chr11 - 88322411 88322411 88322411 TGTTCCTGTTTCTTAATCCATATACGAAAATCAACTTACGATGGATTAAAGACTTAAATGTAAAA TGTTCCTGTTTCTTAATCCATATACGAAAATCGACTTACGATGGATTAAAGACTTAAATGTAAAA T C CTSC Ensembl:ENSG00000109861 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1021712367 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26408906 13656 RMVar_ID_13656 Human_SNP_ID_475955233 A-to-I Human chr11 - 88322452 88322452 88322452 CCTACTGTATATCTGGCTAGCCATATGCAGAAAATTGAAACTGTTCCTGTTTCTTAATCCATATA CCTACTGTATATCTGGCTAGCCATATGCAGAAGATTGAAACTGTTCCTGTTTCTTAATCCATATA T C CTSC Ensembl:ENSG00000109861 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1305971204 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26409908 13657 RMVar_ID_13657 Human_SNP_ID_475955657 A-to-I Human chr11 - 88324165 88324165 88324165 CTAGCCAGTTCTCCCAGCACCATTTATTAAATAGGGAATCCTTTCCCTATTGTTTGTTTTTGTAC CTAGCCAGTTCTCCCAGCACCATTTATTAAATGGGGAATCCTTTCCCTATTGTTTGTTTTTGTAC T C CTSC Ensembl:ENSG00000109861 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs536496337 Functional Loss SNV dbSNP153 33..33 33 - - - 13658 RMVar_ID_13658 Human_SNP_ID_475956793 A-to-I Human chr11 - 88328766 88328766 88328766 AAAAGTAGCCGGGTGTGGTGGTGCACGCCTATAGTCTCAGCCACCTGGGAGGCTGGGGCAGAAGA AAAAGTAGCCGGGTGTGGTGGTGCACGCCTATGGTCTCAGCCACCTGGGAGGCTGGGGCAGAAGA T C CTSC Ensembl:ENSG00000109861 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1169553069 Functional Loss SNV dbSNP153 33..33 33 - - - 13659 RMVar_ID_13659 Human_SNP_ID_475956794 A-to-I Human chr11 - 88328768 88328768 88328768 CAAAAAGTAGCCGGGTGTGGTGGTGCACGCCTATAGTCTCAGCCACCTGGGAGGCTGGGGCAGAA CAAAAAGTAGCCGGGTGTGGTGGTGCACGCCTGTAGTCTCAGCCACCTGGGAGGCTGGGGCAGAA T C CTSC Ensembl:ENSG00000109861 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1173772725 Functional Loss SNV dbSNP153 33..33 33 - - - 13660 RMVar_ID_13660 Human_SNP_ID_475956810 A-to-I Human chr11 - 88328828 88328828 88328828 CCTGAGGTCAGAAGATGGAGTCCAGCCTCAACATGGTGAAACCCCTCTATACTAAAAATACAAAA CCTGAGGTCAGAAGATGGAGTCCAGCCTCAACTTGGTGAAACCCCTCTATACTAAAAATACAAAA T A CTSC Ensembl:ENSG00000109861 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1383118509 Functional Loss SNV dbSNP153 33..33 33 - - - 13661 RMVar_ID_13661 Human_SNP_ID_475956912 A-to-I Human chr11 - 88329264 88329264 88329264 TTGACCAGACTGGTCTTGAACTCCTGACCCCAAGTGATCCGCCCGCCTGGACCTCCCCAAGTGCT TTGACCAGACTGGTCTTGAACTCCTGACCCCAGGTGATCCGCCCGCCTGGACCTCCCCAAGTGCT T C CTSC Ensembl:ENSG00000109861 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1433539242 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24907457 13662 RMVar_ID_13662 Human_SNP_ID_475956940 A-to-I Human chr11 - 88329319 88329319 88329319 CGCCATCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGACCAGAC CGCCATCACGCCCAGCTAATTTTTGTATTTTTGGTAGAGATGGGGTTTCACCATGTTGACCAGAC T C CTSC Ensembl:ENSG00000109861 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1434952036 Functional Loss SNV dbSNP153 33..33 33 - - - 13663 RMVar_ID_13663 Human_SNP_ID_475956945 A-to-I Human chr11 - 88329338 88329338 88329338 AGATTGGATTACAGGTGCCCGCCATCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGT AGATTGGATTACAGGTGCCCGCCATCACGCCCTGCTAATTTTTGTATTTTTAGTAGAGATGGGGT T A CTSC Ensembl:ENSG00000109861 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs995516971 Functional Loss SNV dbSNP153 33..33 33 - - - 13664 RMVar_ID_13664 Human_SNP_ID_475957162 A-to-I Human chr11 - 88329878 88329878 88329878 CACTAAAAATACAAAAATTAGCCAGGCATAGCAGCGCACGCCTGTAGTCCCAGTTACTTGGGAGG CACTAAAAATACAAAAATTAGCCAGGCATAGCGGCGCACGCCTGTAGTCCCAGTTACTTGGGAGG T C CTSC Ensembl:ENSG00000109861 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs217065 Functional Loss SNV dbSNP153 33..33 33 - - - 13665 RMVar_ID_13665 Human_SNP_ID_475957169 A-to-I Human chr11 - 88329891 88329891 88329891 GAAACCTCATCTCCACTAAAAATACAAAAATTAGCCAGGCATAGCAGCGCACGCCTGTAGTCCCA GAAACCTCATCTCCACTAAAAATACAAAAATTGGCCAGGCATAGCAGCGCACGCCTGTAGTCCCA T C CTSC Ensembl:ENSG00000109861 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs762611830 Functional Loss SNV dbSNP153 33..33 33 - - - 13666 RMVar_ID_13666 Human_SNP_ID_476007369 A-to-I Human chr11 - 88521378 88521378 88521378 AGAGTCTGCAATGTCACCCAGGCTGGAGTGCAATGGTGCGATCTTGGCTCACTGCAACTTCTGCC AGAGTCTGCAATGTCACCCAGGCTGGAGTGCAGTGGTGCGATCTTGGCTCACTGCAACTTCTGCC T C GRM5 Ensembl:ENSG00000168959 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs527983898 Functional Loss SNV dbSNP153 33..33 33 - - - 13667 RMVar_ID_13667 Human_SNP_ID_476317664 A-to-I Human chr11 - 89734381 89734381 89734381 AGTGCCACCCTAGAGACCACAGGAAAAGGGCTACTGCTGAAAGTGCTGTTGGTTTTGGTGAAACA AGTGCCACCCTAGAGACCACAGGAAAAGGGCTGCTGCTGAAAGTGCTGTTGGTTTTGGTGAAACA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232893137 Functional Loss SNV dbSNP153 33..33 33 - - - 13668 RMVar_ID_13668 Human_SNP_ID_569966071 A-to-I Human chr15 + 22500262 22500262 22500262 CAGTGGCACTATCTCAGCTCACTGCAACCTCCACCTCCCAGGTTCAAGCCATTCTCGTGCCTCAG CAGTGGCACTATCTCAGCTCACTGCAACCTCCGCCTCCCAGGTTCAAGCCATTCTCGTGCCTCAG A G HERC2P2 Ensembl:ENSG00000276550 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1445121746 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_30159,RMVar_hsa_circ_365711 13669 RMVar_ID_13669 Human_SNP_ID_569966073 A-to-I Human chr15 + 22500269 22500269 22500269 ACTATCTCAGCTCACTGCAACCTCCACCTCCCAGGTTCAAGCCATTCTCGTGCCTCAGCCTCCTA ACTATCTCAGCTCACTGCAACCTCCACCTCCCCGGTTCAAGCCATTCTCGTGCCTCAGCCTCCTA A C HERC2P2 Ensembl:ENSG00000276550 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1186434547 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_30159,RMVar_hsa_circ_365711 13670 RMVar_ID_13670 Human_SNP_ID_570009011 A-to-I Human chr15 + 22680488 22680488 22680488 GGGAGGCTGAGGCAGGAGAATCGCTTGAACCCAGGAGGCGGAAGTTGCAGTGAGCCGAGATCATG GGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGGGAGGCGGAAGTTGCAGTGAGCCGAGATCATG A G WHAMMP3 Ensembl:ENSG00000276141 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1049935346 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_322883 13671 RMVar_ID_13671 Human_SNP_ID_570009012 A-to-I Human chr15 + 22680488 22680488 22680488 GGGAGGCTGAGGCAGGAGAATCGCTTGAACCCAGGAGGCGGAAGTTGCAGTGAGCCGAGATCATG GGGAGGCTGAGGCAGGAGAATCGCTTGAACCCTGGAGGCGGAAGTTGCAGTGAGCCGAGATCATG A T WHAMMP3 Ensembl:ENSG00000276141 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1049935346 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_322883 13672 RMVar_ID_13672 Human_SNP_ID_570037999 A-to-I Human chr15 + 22789092 22789092 22789092 CTTGGCTCACTGAACCTCTGCCTCCCGGGTTCAAGCGATTCGCCTGCCACAGCCTCCCGAGCTGG CTTGGCTCACTGAACCTCTGCCTCCCGGGTTCCAGCGATTCGCCTGCCACAGCCTCCCGAGCTGG A C NIPA1 Ensembl:ENSG00000170113 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1229541007 Functional Loss SNV dbSNP153 33..33 33 - - - 13673 RMVar_ID_13673 Human_SNP_ID_570043631 A-to-I Human chr15 + 22807550 22807550 22807550 GAGGTTGCAGTGAACTGAGAGACCATGCCACTACACCCCAGCCTGGGCAACAGAGTGAGACCCTG GAGGTTGCAGTGAACTGAGAGACCATGCCACTGCACCCCAGCCTGGGCAACAGAGTGAGACCCTG A G NIPA1 Ensembl:ENSG00000170113 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005064610 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25131173 13674 RMVar_ID_13674 Human_SNP_ID_570043756 A-to-I Human chr15 + 22807863 22807863 22807863 TGGAGTGCAGTGGCACAATCTCGGCTTACTGCAAGCTCTGCCTCCCAGGTTCATGCCATTTTCCT TGGAGTGCAGTGGCACAATCTCGGCTTACTGCGAGCTCTGCCTCCCAGGTTCATGCCATTTTCCT A G NIPA1 Ensembl:ENSG00000170113 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256838683 Functional Loss SNV dbSNP153 33..33 33 - - - 13675 RMVar_ID_13675 Human_SNP_ID_570052552 A-to-I Human chr15 + 22839265 22839261 22839265 CCTTAGAAGTCTGCTGTGACGTTTTGAGCCTGACTGTTTTAATTTCCTTTTATAAAATCACGGAA CCTTAGAAGTCTGCTGTGACGTTTTGAGC____CTGTTTTAATTTCCTTTTATAAAATCACGGAA CCTGA C NIPA2 Ensembl:ENSG00000140157 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1220290769 Functional Loss DEL dbSNP153 30..33 33 - - - 13676 RMVar_ID_13676 Human_SNP_ID_570052553 A-to-I Human chr15 + 22839265 22839265 22839265 CCTTAGAAGTCTGCTGTGACGTTTTGAGCCTGACTGTTTTAATTTCCTTTTATAAAATCACGGAA CCTTAGAAGTCTGCTGTGACGTTTTGAGCCTGGCTGTTTTAATTTCCTTTTATAAAATCACGGAA A G NIPA2 Ensembl:ENSG00000140157 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4592619 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_1110,GWAS_ID_1111,GWAS_ID_1112,GWAS_ID_1113,GWAS_ID_1114 13677 RMVar_ID_13677 Human_SNP_ID_570052780 A-to-I Human chr15 + 22840076 22840076 22840076 CCCAGCAGCTGGGACCACAGACGTGCGGCACCATGCCTGGCTAATTTTTGTATTTTTTTTAGAAC CCCAGCAGCTGGGACCACAGACGTGCGGCACCGTGCCTGGCTAATTTTTGTATTTTTTTTAGAAC A G NIPA2 Ensembl:ENSG00000140157 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1000370745 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_189,RMVar_hsa_circ_299848,RMVar_hsa_circ_359808,RMVar_hsa_circ_17764 13678 RMVar_ID_13678 Human_SNP_ID_570053846 A-to-I Human chr15 + 22843263 22843263 22843263 GCGGTGGCTCACGCCTGTAATCCCAGCACTTTAGGAGGCCAAGGCTGTTGGATCACGAGGTCAGG GCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCTGTTGGATCACGAGGTCAGG A G NIPA2 Ensembl:ENSG00000140157 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1320109804 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12481015 RMVar_hsa_circ_189,RMVar_hsa_circ_299848,RMVar_hsa_circ_359808,RMVar_hsa_circ_17764,RMVar_hsa_circ_309750,RMVar_hsa_circ_330066 13679 RMVar_ID_13679 Human_SNP_ID_570057060 A-to-I Human chr15 + 22853935 22853935 22853935 CTGCAGCCTTCGCCTCCCGGGTTCAAGCGATTATCCTGCCTCATCCTCCTGAGTAGCTGAGACTA CTGCAGCCTTCGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCATCCTCCTGAGTAGCTGAGACTA A C NIPA2 Ensembl:ENSG00000140157 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs903984666 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_189,RMVar_hsa_circ_17764,RMVar_hsa_circ_20603,RMVar_hsa_circ_19158,RMVar_hsa_circ_330388,RMVar_hsa_circ_326767,RMVar_hsa_circ_361653,RMVar_hsa_circ_28898 13680 RMVar_ID_13680 Human_SNP_ID_570057067 A-to-I Human chr15 + 22853962 22853961 22853962 CGATTATCCTGCCTCATCCTCCTGAGTAGCTGAGACTACTGGTGCGCACCACTATGCCCAGCTAA CGATTATCCTGCCTCATCCTCCTGAGTAGCTG_GACTACTGGTGCGCACCACTATGCCCAGCTAA GA G NIPA2 Ensembl:ENSG00000140157 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1383118379 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_189,RMVar_hsa_circ_17764,RMVar_hsa_circ_20603,RMVar_hsa_circ_19158,RMVar_hsa_circ_330388,RMVar_hsa_circ_326767,RMVar_hsa_circ_361653,RMVar_hsa_circ_28898 13681 RMVar_ID_13681 Human_SNP_ID_570057084 A-to-I Human chr15 + 22854017 22854016 22854018 GCCCAGCTAATTTTTGTATTTTTAGTAGAGACAGGGATTCACACGTTGGCCAGGCTGGTCTCGAT GCCCAGCTAATTTTTGTATTTTTAGTAGAGAC__GGATTCACACGTTGGCCAGGCTGGTCTCGAT CAG C NIPA2 Ensembl:ENSG00000140157 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs369295410 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_189,RMVar_hsa_circ_17764,RMVar_hsa_circ_20603,RMVar_hsa_circ_19158,RMVar_hsa_circ_330388,RMVar_hsa_circ_326767,RMVar_hsa_circ_361653,RMVar_hsa_circ_28898 13682 RMVar_ID_13682 Human_SNP_ID_570057085 A-to-I Human chr15 + 22854017 22854017 22854017 GCCCAGCTAATTTTTGTATTTTTAGTAGAGACAGGGATTCACACGTTGGCCAGGCTGGTCTCGAT GCCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGATTCACACGTTGGCCAGGCTGGTCTCGAT A G NIPA2 Ensembl:ENSG00000140157 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs887375556 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_189,RMVar_hsa_circ_17764,RMVar_hsa_circ_20603,RMVar_hsa_circ_19158,RMVar_hsa_circ_330388,RMVar_hsa_circ_326767,RMVar_hsa_circ_361653,RMVar_hsa_circ_28898 13683 RMVar_ID_13683 Human_SNP_ID_570057159 A-to-I Human chr15 + 22854227 22854227 22854227 TTGGCTCACTGCAACCTCTGCCTCCTGGGTTCAAGCGATTCTCCTGCCTCATCCTCCTGAGTAGC TTGGCTCACTGCAACCTCTGCCTCCTGGGTTCCAGCGATTCTCCTGCCTCATCCTCCTGAGTAGC A C NIPA2 Ensembl:ENSG00000140157 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs971208281 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_189,RMVar_hsa_circ_17764,RMVar_hsa_circ_20603,RMVar_hsa_circ_19158,RMVar_hsa_circ_330388,RMVar_hsa_circ_326767,RMVar_hsa_circ_361653,RMVar_hsa_circ_28898 13684 RMVar_ID_13684 Human_SNP_ID_570057160 A-to-I Human chr15 + 22854227 22854227 22854227 TTGGCTCACTGCAACCTCTGCCTCCTGGGTTCAAGCGATTCTCCTGCCTCATCCTCCTGAGTAGC TTGGCTCACTGCAACCTCTGCCTCCTGGGTTCGAGCGATTCTCCTGCCTCATCCTCCTGAGTAGC A G NIPA2 Ensembl:ENSG00000140157 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs971208281 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_189,RMVar_hsa_circ_17764,RMVar_hsa_circ_20603,RMVar_hsa_circ_19158,RMVar_hsa_circ_330388,RMVar_hsa_circ_326767,RMVar_hsa_circ_361653,RMVar_hsa_circ_28898 13685 RMVar_ID_13685 Human_SNP_ID_570057449 A-to-I Human chr15 + 22855227 22855227 22855227 CTGAGGTCAGGAGTGAGACCAGCCTGACCAACATGGAGAAACCTCGTCTCTAGTAAAAAAAAAAA CTGAGGTCAGGAGTGAGACCAGCCTGACCAACGTGGAGAAACCTCGTCTCTAGTAAAAAAAAAAA A G NIPA2 Ensembl:ENSG00000140157 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1394099896 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_189,RMVar_hsa_circ_17764,RMVar_hsa_circ_20603,RMVar_hsa_circ_19158,RMVar_hsa_circ_330388,RMVar_hsa_circ_326767,RMVar_hsa_circ_361653,RMVar_hsa_circ_28898 13686 RMVar_ID_13686 Human_SNP_ID_570057469 A-to-I Human chr15 + 22855306 22855306 22855306 GGGCATGGTGGTGCATGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGGA GGGCATGGTGGTGCATGCCTGTAATCCCAGCTGCTCGGGAGGCTGAGGCAGGAGAATCGCTTGGA A G NIPA2 Ensembl:ENSG00000140157 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs532374643 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_189,RMVar_hsa_circ_17764,RMVar_hsa_circ_20603,RMVar_hsa_circ_19158,RMVar_hsa_circ_330388,RMVar_hsa_circ_326767,RMVar_hsa_circ_361653,RMVar_hsa_circ_28898 13687 RMVar_ID_13687 Human_SNP_ID_570057484 A-to-I Human chr15 + 22855349 22855349 22855349 TGAGGCAGGAGAATCGCTTGGACCTGAAAGGCAGAGGTTACAGTGAGCTGAGATTGTGCCGTTGC TGAGGCAGGAGAATCGCTTGGACCTGAAAGGCGGAGGTTACAGTGAGCTGAGATTGTGCCGTTGC A G NIPA2 Ensembl:ENSG00000140157 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs962211046 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_189,RMVar_hsa_circ_17764,RMVar_hsa_circ_20603,RMVar_hsa_circ_19158,RMVar_hsa_circ_330388,RMVar_hsa_circ_326767,RMVar_hsa_circ_361653,RMVar_hsa_circ_28898 13688 RMVar_ID_13688 Human_SNP_ID_570060301 A-to-I Human chr15 + 22864898 22864898 22864898 TCCTCTCTTTTTTCTTGAGACAGTCTCACTCTATTGCCCAGGCTGGAGTGCAGTGGCATGATCTC TCCTCTCTTTTTTCTTGAGACAGTCTCACTCTGTTGCCCAGGCTGGAGTGCAGTGGCATGATCTC A G NIPA2 Ensembl:ENSG00000140157 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1246818355 Functional Loss SNV dbSNP153 33..33 33 - - - 13689 RMVar_ID_13689 Human_SNP_ID_570071096 A-to-I Human chr15 - 22898881 22898881 22898881 TCCCCTGCCTTAGCCTCCCGATTAGCTGGACTATAGTCGCCCGCCACCACGCCCGGCTAATTTTT TCCCCTGCCTTAGCCTCCCGATTAGCTGGACTGTAGTCGCCCGCCACCACGCCCGGCTAATTTTT T C CYFIP1 Ensembl:ENSG00000273749 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs774853186 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44122,RMVar_hsa_circ_33701,RMVar_hsa_circ_67509 13690 RMVar_ID_13690 Human_SNP_ID_570101090 A-to-I Human chr15 - 22999378 22999378 22999378 CCACTTGCCCACAGTCCAGACAGATGGATTGTAGGTGGGTTTTCTGGAGATTAGTAGATACTGTA CCACTTGCCCACAGTCCAGACAGATGGATTGTGGGTGGGTTTTCTGGAGATTAGTAGATACTGTA T C TUBGCP5 Ensembl:ENSG00000275835 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-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 13691 RMVar_ID_13691 Human_SNP_ID_570604990 A-to-I Human chr15 - 24909020 24909020 24909020 CAAGAAAGAAGTTAAAAAGAAGAGGTGGAACCATCCCAAAATGTCCCTTGCTCAGAAGAAGGATT CAAGAAAGAAGTTAAAAAGAAGAGGTGGAACCGTCCCAAAATGTCCCTTGCTCAGAAGAAGGATT T C RPL5P1 Ensembl:ENSG00000241061 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879012126 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17368032 13692 RMVar_ID_13692 Human_SNP_ID_570605149 A-to-I Human chr15 - 24909658 24909658 24909658 AACACACTCAAATACAGGATGATAGTTCGTGTAACAAACAGAGATATCATTTGTCAGATTGCTTA AACACACTCAAATACAGGATGATAGTTCGTGTGACAAACAGAGATATCATTTGTCAGATTGCTTA T C RPL5P1 Ensembl:ENSG00000241061 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879041330 Functional Loss SNV dbSNP153 33..33 33 - - - 13693 RMVar_ID_13693 Human_SNP_ID_570605194 A-to-I Human chr15 + 24909831 24909830 24909831 ATTCTTAACAACTTTAACAAACCCCATCCTGCAGAACAGAGACCCGCGTCCACAGCTCAACAGAG ATTCTTAACAACTTTAACAAACCCCATCCTGC_GAACAGAGACCCGCGTCCACAGCTCAACAGAG CA C AC090983.2,SNRPN Ensembl:ENSG00000286110,Ensembl:ENSG00000128739 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1340252338 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_9048989 RMVar_hsa_circ_39838,RMVar_hsa_circ_11327 13694 RMVar_ID_13694 Human_SNP_ID_570606787 A-to-I Human chr15 + 24916455 24916455 24916455 CTCAGCCTGTAGTCCCAGTTACTTAGGAGGCTAAGGCAGGAGGATTGCTTGAGCCCAGAAACTCA CTCAGCCTGTAGTCCCAGTTACTTAGGAGGCTGAGGCAGGAGGATTGCTTGAGCCCAGAAACTCA A G SNRPN Ensembl:ENSG00000128739 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs552935195 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39838,RMVar_hsa_circ_11327 13695 RMVar_ID_13695 Human_SNP_ID_570620211 A-to-I Human chr15 + 24963870 24963870 24963870 CAGCCTGGGCAACATAGAGAGACCTCCTCTCTACAGAAAAATAAATTAGCCAGGCGTGGTGTTGT CAGCCTGGGCAACATAGAGAGACCTCCTCTCTGCAGAAAAATAAATTAGCCAGGCGTGGTGTTGT A G SNURF,SNRPN,AC124312.1 Ensembl:ENSG00000273173,Ensembl:ENSG00000128739,Ensembl:ENSG00000214265 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs372917124 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_170099 13696 RMVar_ID_13696 Human_SNP_ID_570620361 A-to-I Human chr15 + 24964392 24964392 24964392 AGGATGGAGTGCAACCTCCGCCTACCAAGTTCAAGTGATTCTCCTGCCTCAGTCTCCCAAGTAAC AGGATGGAGTGCAACCTCCGCCTACCAAGTTCTAGTGATTCTCCTGCCTCAGTCTCCCAAGTAAC A T SNURF,SNRPN,AC124312.1 Ensembl:ENSG00000273173,Ensembl:ENSG00000128739,Ensembl:ENSG00000214265 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1188174849 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_170099 13697 RMVar_ID_13697 Human_SNP_ID_570620386 A-to-I Human chr15 + 24964494 24964494 24964494 TTGTATTTTTTTAGTAGAGACAGGGTTTCTCCATGTTGGTCAGGCTGGGCTCGAACTCCCGACCT TTGTATTTTTTTAGTAGAGACAGGGTTTCTCCGTGTTGGTCAGGCTGGGCTCGAACTCCCGACCT A G SNURF,SNRPN,AC124312.1 Ensembl:ENSG00000273173,Ensembl:ENSG00000128739,Ensembl:ENSG00000214265 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1206193693 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_170099 13698 RMVar_ID_13698 Human_SNP_ID_570620407 A-to-I Human chr15 + 24964559 24964559 24964559 CAGATGATCCGCCCGCCTTGGTTTCTTTCCCAAAGTGCTAGGATTACAGGTGTGAGCCACTGCGC CAGATGATCCGCCCGCCTTGGTTTCTTTCCCAGAGTGCTAGGATTACAGGTGTGAGCCACTGCGC A G SNURF,SNRPN,AC124312.1 Ensembl:ENSG00000273173,Ensembl:ENSG00000128739,Ensembl:ENSG00000214265 Protein coding,Protein coding,Protein coding intron,intron,intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs572080501 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_170099 13699 RMVar_ID_13699 Human_SNP_ID_570620408 A-to-I Human chr15 + 24964559 24964559 24964559 CAGATGATCCGCCCGCCTTGGTTTCTTTCCCAAAGTGCTAGGATTACAGGTGTGAGCCACTGCGC CAGATGATCCGCCCGCCTTGGTTTCTTTCCCATAGTGCTAGGATTACAGGTGTGAGCCACTGCGC A T SNURF,SNRPN,AC124312.1 Ensembl:ENSG00000273173,Ensembl:ENSG00000128739,Ensembl:ENSG00000214265 Protein coding,Protein coding,Protein coding intron,intron,intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs572080501 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_170099 13700 RMVar_ID_13700 Human_SNP_ID_570620412 A-to-I Human chr15 + 24964581 24964581 24964581 TTCTTTCCCAAAGTGCTAGGATTACAGGTGTGAGCCACTGCGCCCAGCCTCTCCCTTCATTCTTT TTCTTTCCCAAAGTGCTAGGATTACAGGTGTGGGCCACTGCGCCCAGCCTCTCCCTTCATTCTTT A G SNURF,SNRPN,AC124312.1 Ensembl:ENSG00000273173,Ensembl:ENSG00000128739,Ensembl:ENSG00000214265 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1198847032 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_170099 13701 RMVar_ID_13701 Human_SNP_ID_570620606 A-to-I Human chr15 + 24965403 24965403 24965403 CTAGAAAAATAAAAAAATCAGCCGGGTGTGGTAGTGTGCACCTGTAATCCCAGCTACTCAGGAGG CTAGAAAAATAAAAAAATCAGCCGGGTGTGGTGGTGTGCACCTGTAATCCCAGCTACTCAGGAGG A G SNURF,SNRPN,AC124312.1 Ensembl:ENSG00000273173,Ensembl:ENSG00000128739,Ensembl:ENSG00000214265 Protein coding,Protein coding,Protein coding intron,intron,intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1416195676 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_170099 13702 RMVar_ID_13702 Human_SNP_ID_570621169 A-to-I Human chr15 + 24967469 24967469 24967469 CCAGATCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAAAATTAGCCGAG CCAGATCAGCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAAAATTAGCCGAG A G SNURF,SNRPN,AC124312.1 Ensembl:ENSG00000273173,Ensembl:ENSG00000128739,Ensembl:ENSG00000214265 Protein coding,Protein coding,Protein coding intron,intron,intron GSE107867 ASD brains,cerebellum;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1296842530 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 13703 RMVar_ID_13703 Human_SNP_ID_570621699 A-to-I Human chr15 + 24969153 24969153 24969153 GAGTTATTAATTAATTTATTTATTTAGAGATGAAGTTTCACTCTGTTGCCCAGGCTGGAGTGCAG GAGTTATTAATTAATTTATTTATTTAGAGATGGAGTTTCACTCTGTTGCCCAGGCTGGAGTGCAG A G SNURF,SNRPN,AC124312.1 Ensembl:ENSG00000273173,Ensembl:ENSG00000128739,Ensembl:ENSG00000214265 Protein coding,Protein coding,Protein coding intron,intron,intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1219101047 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2016,RMVar_hsa_circ_78132,RMVar_hsa_circ_93848,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_303543,RMVar_hsa_circ_69255,RMVar_hsa_circ_283092,RMVar_hsa_circ_285930,RMVar_hsa_circ_268916 13704 RMVar_ID_13704 Human_SNP_ID_570621759 A-to-I Human chr15 + 24969349 24969348 24969349 CGGGGTTTCACCATGTTCTCCAGGCTGGTCTCAAACTCCTGAACTCAGGTGATCCACCTGCCTTG CGGGGTTTCACCATGTTCTCCAGGCTGGTCTC_AACTCCTGAACTCAGGTGATCCACCTGCCTTG CA C SNURF,SNRPN,AC124312.1 Ensembl:ENSG00000273173,Ensembl:ENSG00000128739,Ensembl:ENSG00000214265 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1284570705 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_2016,RMVar_hsa_circ_78132,RMVar_hsa_circ_93848,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_303543,RMVar_hsa_circ_69255,RMVar_hsa_circ_283092,RMVar_hsa_circ_285930,RMVar_hsa_circ_268916 13705 RMVar_ID_13705 Human_SNP_ID_570622001 A-to-I Human chr15 + 24970325 24970325 24970325 AATGTGGCCGGGTGTGGTGGCTCACGCCTGTCATCCTAGCACTTGGGGAGGCTGAGGCAGGTGGA AATGTGGCCGGGTGTGGTGGCTCACGCCTGTCGTCCTAGCACTTGGGGAGGCTGAGGCAGGTGGA A G SNURF,SNRPN,AC124312.1 Ensembl:ENSG00000273173,Ensembl:ENSG00000128739,Ensembl:ENSG00000214265 Protein coding,Protein coding,Protein coding intron,intron,intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs886380845 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2016,RMVar_hsa_circ_78132,RMVar_hsa_circ_93848,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_303543,RMVar_hsa_circ_69255,RMVar_hsa_circ_283092,RMVar_hsa_circ_285930,RMVar_hsa_circ_268916 13706 RMVar_ID_13706 Human_SNP_ID_570622489 A-to-I Human chr15 + 24972094 24972093 24972094 CCTGGCCAACGTAGCGAAATTCCTTCTCTGCTAAAAATACAAAAATTAGCCGGGTGTGGTGGCGG CCTGGCCAACGTAGCGAAATTCCTTCTCTGCT_AAAATACAAAAATTAGCCGGGTGTGGTGGCGG TA T SNURF,SNRPN,AC124312.1 Ensembl:ENSG00000273173,Ensembl:ENSG00000128739,Ensembl:ENSG00000214265 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1366178713 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_2016,RMVar_hsa_circ_78132,RMVar_hsa_circ_93848,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_303543,RMVar_hsa_circ_69255,RMVar_hsa_circ_283092,RMVar_hsa_circ_285930,RMVar_hsa_circ_268916 13707 RMVar_ID_13707 Human_SNP_ID_570622493 A-to-I Human chr15 + 24972109 24972109 24972109 GAAATTCCTTCTCTGCTAAAAATACAAAAATTAGCCGGGTGTGGTGGCGGGCGCCTGTAATCCTA GAAATTCCTTCTCTGCTAAAAATACAAAAATTGGCCGGGTGTGGTGGCGGGCGCCTGTAATCCTA A G SNURF,SNRPN,AC124312.1 Ensembl:ENSG00000273173,Ensembl:ENSG00000128739,Ensembl:ENSG00000214265 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1043143072 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2016,RMVar_hsa_circ_78132,RMVar_hsa_circ_93848,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_303543,RMVar_hsa_circ_69255,RMVar_hsa_circ_283092,RMVar_hsa_circ_285930,RMVar_hsa_circ_268916 13708 RMVar_ID_13708 Human_SNP_ID_570622802 A-to-I Human chr15 + 24973163 24973163 24973163 CGCCCACCTCGGTTTCCCAAAGTGTTGGGATTATGGGCGTGAGCCACCACACCCAGCCTCTTCTC CGCCCACCTCGGTTTCCCAAAGTGTTGGGATTTTGGGCGTGAGCCACCACACCCAGCCTCTTCTC A T SNURF,SNRPN,AC124312.1 Ensembl:ENSG00000273173,Ensembl:ENSG00000128739,Ensembl:ENSG00000214265 Protein coding,Protein coding,Protein coding intron,intron,intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs894920464 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2016,RMVar_hsa_circ_78132,RMVar_hsa_circ_93848,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_303543,RMVar_hsa_circ_69255,RMVar_hsa_circ_283092,RMVar_hsa_circ_285930,RMVar_hsa_circ_268916 13709 RMVar_ID_13709 Human_SNP_ID_570625467 A-to-I Human chr15 + 24982618 24982618 24982618 AGGCAGCATTGCTAATTTTTGTATAGTGAGACAGTATCTCACAGTCCAGGCTGGAGTTCAGTGGC AGGCAGCATTGCTAATTTTTGTATAGTGAGACGGTATCTCACAGTCCAGGCTGGAGTTCAGTGGC A G SNHG14,AC124312.1 Ensembl:ENSG00000224078,Ensembl:ENSG00000214265 lincRNA,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs3195946 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9049139 RMVar_hsa_circ_33239,RMVar_hsa_circ_2016,RMVar_hsa_circ_23619,RMVar_hsa_circ_357218,RMVar_hsa_circ_69255,RMVar_hsa_circ_32424,RMVar_hsa_circ_36518,RMVar_hsa_circ_28999,RMVar_hsa_circ_170109,RMVar_hsa_circ_170110 13710 RMVar_ID_13710 Human_SNP_ID_570625480 A-to-I Human chr15 + 24982690 24982690 24982690 TAACTCACTGCAGCCTTGAACACCTGAGCTCAAACGATCCTTTCACCTTATCCTCCAGAGTAGCT TAACTCACTGCAGCCTTGAACACCTGAGCTCAGACGATCCTTTCACCTTATCCTCCAGAGTAGCT A G SNHG14,AC124312.1 Ensembl:ENSG00000224078,Ensembl:ENSG00000214265 lincRNA,Protein coding exon,intron GSE47997;GSE100210;GSE107867;GSE107867 K562 cells&HepG2 cells;HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank;ASD brains,temporal_cortex - 23474544,29129909,30559470,30559470 RNA-Seq:(High) rs907116223 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33239,RMVar_hsa_circ_2016,RMVar_hsa_circ_23619,RMVar_hsa_circ_357218,RMVar_hsa_circ_69255,RMVar_hsa_circ_32424,RMVar_hsa_circ_36518,RMVar_hsa_circ_28999,RMVar_hsa_circ_170109,RMVar_hsa_circ_170110 13711 RMVar_ID_13711 Human_SNP_ID_570625487 A-to-I Human chr15 + 24982707 24982707 24982707 GAACACCTGAGCTCAAACGATCCTTTCACCTTATCCTCCAGAGTAGCTGGGACTACAGTCGCGTG GAACACCTGAGCTCAAACGATCCTTTCACCTTGTCCTCCAGAGTAGCTGGGACTACAGTCGCGTG A G SNHG14,AC124312.1 Ensembl:ENSG00000224078,Ensembl:ENSG00000214265 lincRNA,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1133857 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33239,RMVar_hsa_circ_2016,RMVar_hsa_circ_23619,RMVar_hsa_circ_357218,RMVar_hsa_circ_69255,RMVar_hsa_circ_32424,RMVar_hsa_circ_36518,RMVar_hsa_circ_28999,RMVar_hsa_circ_170109,RMVar_hsa_circ_170110 13712 RMVar_ID_13712 Human_SNP_ID_570625490 A-to-I Human chr15 + 24982714 24982714 24982714 TGAGCTCAAACGATCCTTTCACCTTATCCTCCAGAGTAGCTGGGACTACAGTCGCGTGTCAACAT TGAGCTCAAACGATCCTTTCACCTTATCCTCCGGAGTAGCTGGGACTACAGTCGCGTGTCAACAT A G SNHG14,AC124312.1 Ensembl:ENSG00000224078,Ensembl:ENSG00000214265 lincRNA,Protein coding exon,intron GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 29129909,30559470 RNA-Seq:(High) rs1001239015 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33239,RMVar_hsa_circ_2016,RMVar_hsa_circ_23619,RMVar_hsa_circ_357218,RMVar_hsa_circ_69255,RMVar_hsa_circ_32424,RMVar_hsa_circ_36518,RMVar_hsa_circ_28999,RMVar_hsa_circ_170109,RMVar_hsa_circ_170110 13713 RMVar_ID_13713 Human_SNP_ID_570625493 A-to-I Human chr15 + 24982719 24982719 24982719 TCAAACGATCCTTTCACCTTATCCTCCAGAGTAGCTGGGACTACAGTCGCGTGTCAACATGCCTG TCAAACGATCCTTTCACCTTATCCTCCAGAGTGGCTGGGACTACAGTCGCGTGTCAACATGCCTG A G SNHG14,AC124312.1 Ensembl:ENSG00000224078,Ensembl:ENSG00000214265 lincRNA,Protein coding exon,intron GSE100210;GSE107867 HepG2 cell line;ASD brains,cerebellum - 29129909,30559470 RNA-Seq:(High) rs1034098417 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17563145 RMVar_hsa_circ_33239,RMVar_hsa_circ_2016,RMVar_hsa_circ_23619,RMVar_hsa_circ_357218,RMVar_hsa_circ_69255,RMVar_hsa_circ_32424,RMVar_hsa_circ_36518,RMVar_hsa_circ_28999,RMVar_hsa_circ_170109,RMVar_hsa_circ_170110 13714 RMVar_ID_13714 Human_SNP_ID_570625496 A-to-I Human chr15 + 24982731 24982731 24982731 TTCACCTTATCCTCCAGAGTAGCTGGGACTACAGTCGCGTGTCAACATGCCTGGCTAATTTTAGT TTCACCTTATCCTCCAGAGTAGCTGGGACTACGGTCGCGTGTCAACATGCCTGGCTAATTTTAGT A G SNHG14,AC124312.1 Ensembl:ENSG00000224078,Ensembl:ENSG00000214265 lincRNA,Protein coding exon,intron GSE100210;GSE107867 HepG2 cell line;ASD brains,cerebellum - 29129909,30559470 RNA-Seq:(High) rs1011710053 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17563145 RMVar_hsa_circ_33239,RMVar_hsa_circ_2016,RMVar_hsa_circ_23619,RMVar_hsa_circ_357218,RMVar_hsa_circ_69255,RMVar_hsa_circ_32424,RMVar_hsa_circ_36518,RMVar_hsa_circ_28999,RMVar_hsa_circ_170109,RMVar_hsa_circ_170110 13715 RMVar_ID_13715 Human_SNP_ID_570625519 A-to-I Human chr15 + 24982792 24982792 24982792 TAGTTTTCTAATTTTTTTAGAGTTGGGATCTCACTATGTTGCTTAGACTGGTCTTGAACTCCTGG TAGTTTTCTAATTTTTTTAGAGTTGGGATCTCGCTATGTTGCTTAGACTGGTCTTGAACTCCTGG A G SNHG14,AC124312.1 Ensembl:ENSG00000224078,Ensembl:ENSG00000214265 lincRNA,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1194706265 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9049142,Human_RBP_ID_17563146 RMVar_hsa_circ_33239,RMVar_hsa_circ_2016,RMVar_hsa_circ_23619,RMVar_hsa_circ_357218,RMVar_hsa_circ_69255,RMVar_hsa_circ_32424,RMVar_hsa_circ_36518,RMVar_hsa_circ_28999,RMVar_hsa_circ_170109,RMVar_hsa_circ_170110 13716 RMVar_ID_13716 Human_SNP_ID_570625521 A-to-I Human chr15 + 24982795 24982795 24982795 TTTTCTAATTTTTTTAGAGTTGGGATCTCACTATGTTGCTTAGACTGGTCTTGAACTCCTGGCCT TTTTCTAATTTTTTTAGAGTTGGGATCTCACTCTGTTGCTTAGACTGGTCTTGAACTCCTGGCCT A C SNHG14,AC124312.1 Ensembl:ENSG00000224078,Ensembl:ENSG00000214265 lincRNA,Protein coding exon,intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs933439895 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9049142,Human_RBP_ID_17563146 RMVar_hsa_circ_33239,RMVar_hsa_circ_2016,RMVar_hsa_circ_23619,RMVar_hsa_circ_357218,RMVar_hsa_circ_69255,RMVar_hsa_circ_32424,RMVar_hsa_circ_36518,RMVar_hsa_circ_28999,RMVar_hsa_circ_170109,RMVar_hsa_circ_170110 13717 RMVar_ID_13717 Human_SNP_ID_570625522 A-to-I Human chr15 + 24982795 24982795 24982795 TTTTCTAATTTTTTTAGAGTTGGGATCTCACTATGTTGCTTAGACTGGTCTTGAACTCCTGGCCT TTTTCTAATTTTTTTAGAGTTGGGATCTCACTGTGTTGCTTAGACTGGTCTTGAACTCCTGGCCT A G SNHG14,AC124312.1 Ensembl:ENSG00000224078,Ensembl:ENSG00000214265 lincRNA,Protein coding exon,intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs933439895 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9049142,Human_RBP_ID_17563146 RMVar_hsa_circ_33239,RMVar_hsa_circ_2016,RMVar_hsa_circ_23619,RMVar_hsa_circ_357218,RMVar_hsa_circ_69255,RMVar_hsa_circ_32424,RMVar_hsa_circ_36518,RMVar_hsa_circ_28999,RMVar_hsa_circ_170109,RMVar_hsa_circ_170110 13718 RMVar_ID_13718 Human_SNP_ID_570625666 A-to-I Human chr15 + 24983285 24983285 24983285 GTGGTGGCAGGCACCTGTAATCCCAACTACGCAGGAGGCTAAGGCAGGAGAATTGCTTGAACCCG GTGGTGGCAGGCACCTGTAATCCCAACTACGCGGGAGGCTAAGGCAGGAGAATTGCTTGAACCCG A G SNHG14,AC124312.1 Ensembl:ENSG00000224078,Ensembl:ENSG00000214265 lincRNA,Protein coding exon,intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1478977693 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33239,RMVar_hsa_circ_2016,RMVar_hsa_circ_23619,RMVar_hsa_circ_357218,RMVar_hsa_circ_69255,RMVar_hsa_circ_32424,RMVar_hsa_circ_36518,RMVar_hsa_circ_28999,RMVar_hsa_circ_170109,RMVar_hsa_circ_170110 13719 RMVar_ID_13719 Human_SNP_ID_570625668 A-to-I Human chr15 + 24983293 24983293 24983293 AGGCACCTGTAATCCCAACTACGCAGGAGGCTAAGGCAGGAGAATTGCTTGAACCCGGGAGGCGG AGGCACCTGTAATCCCAACTACGCAGGAGGCTGAGGCAGGAGAATTGCTTGAACCCGGGAGGCGG A G SNHG14,AC124312.1 Ensembl:ENSG00000224078,Ensembl:ENSG00000214265 lincRNA,Protein coding exon,intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1440320042 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33239,RMVar_hsa_circ_2016,RMVar_hsa_circ_23619,RMVar_hsa_circ_357218,RMVar_hsa_circ_69255,RMVar_hsa_circ_32424,RMVar_hsa_circ_36518,RMVar_hsa_circ_28999,RMVar_hsa_circ_170109,RMVar_hsa_circ_170110 13720 RMVar_ID_13720 Human_SNP_ID_570625802 A-to-I Human chr15 + 24983729 24983729 24983729 AGAATCACTTGAACCTGGGCGGCAAAGGTTGCAGTGAGCCGAGACCATGCCACTGCACTCCAGCC AGAATCACTTGAACCTGGGCGGCAAAGGTTGCCGTGAGCCGAGACCATGCCACTGCACTCCAGCC A C SNHG14,AC124312.1 Ensembl:ENSG00000224078,Ensembl:ENSG00000214265 lincRNA,Protein coding exon,intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1331431449 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33239,RMVar_hsa_circ_2016,RMVar_hsa_circ_23619,RMVar_hsa_circ_357218,RMVar_hsa_circ_69255,RMVar_hsa_circ_32424,RMVar_hsa_circ_36518,RMVar_hsa_circ_28999,RMVar_hsa_circ_170109,RMVar_hsa_circ_170110 13721 RMVar_ID_13721 Human_SNP_ID_570625811 A-to-I Human chr15 + 24983748 24983748 24983748 CGGCAAAGGTTGCAGTGAGCCGAGACCATGCCACTGCACTCCAGCCTGGGTGACAGAGTGAGACT CGGCAAAGGTTGCAGTGAGCCGAGACCATGCCGCTGCACTCCAGCCTGGGTGACAGAGTGAGACT A G SNHG14,AC124312.1 Ensembl:ENSG00000224078,Ensembl:ENSG00000214265 lincRNA,Protein coding exon,intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs570577169 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33239,RMVar_hsa_circ_2016,RMVar_hsa_circ_23619,RMVar_hsa_circ_357218,RMVar_hsa_circ_69255,RMVar_hsa_circ_32424,RMVar_hsa_circ_36518,RMVar_hsa_circ_28999,RMVar_hsa_circ_170109,RMVar_hsa_circ_170110 13722 RMVar_ID_13722 Human_SNP_ID_570633495 A-to-I Human chr15 + 25012723 25012723 25012723 TGCCCGCCTCAGCCTCCCAAAGTGTTAGGATTACAGGCATGAGCTACCACGCCCGGCCCATAAAA TGCCCGCCTCAGCCTCCCAAAGTGTTAGGATTGCAGGCATGAGCTACCACGCCCGGCCCATAAAA A G SNHG14 Ensembl:ENSG00000224078 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1454795992 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2016,RMVar_hsa_circ_357218,RMVar_hsa_circ_69255,RMVar_hsa_circ_36518,RMVar_hsa_circ_170110,RMVar_hsa_circ_103034,RMVar_hsa_circ_92185,RMVar_hsa_circ_170124,RMVar_hsa_circ_335469,RMVar_hsa_circ_330039,RMVar_hsa_circ_170125,RMVar_hsa_circ_126273,RMVar_hsa_circ_56667,RMVar_hsa_circ_81621,RMVar_hsa_circ_170127,RMVar_hsa_circ_170126,RMVar_hsa_circ_170129,RMVar_hsa_circ_323040,RMVar_hsa_circ_170130 13723 RMVar_ID_13723 Human_SNP_ID_570638349 A-to-I Human chr15 + 25031731 25031731 25031731 TCTCACCTTAACCTACCCACTCCTAAGTAGCTAGAACTACAGGTGCATGCCACCACGCTCAGCTA TCTCACCTTAACCTACCCACTCCTAAGTAGCTTGAACTACAGGTGCATGCCACCACGCTCAGCTA A T SNHG14 Ensembl:ENSG00000224078 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1033883141 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2016,RMVar_hsa_circ_357218,RMVar_hsa_circ_69255,RMVar_hsa_circ_36518 13724 RMVar_ID_13724 Human_SNP_ID_570675770 A-to-I Human chr15 + 25166784 25166784 25166784 GGGAGGCAGAGGTTGCAGTGAGCCGAGATCGTACCACTGCACTCTGGCCTGGCAACAGAGCGAGA GGGAGGCAGAGGTTGCAGTGAGCCGAGATCGTGCCACTGCACTCTGGCCTGGCAACAGAGCGAGA A G SNHG14 Ensembl:ENSG00000224078 lincRNA intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1164314200 Functional Loss SNV dbSNP153 33..33 33 - - - 13725 RMVar_ID_13725 Human_SNP_ID_570726299 A-to-I Human chr15 + 25334465 25334465 25334465 TCATGGAACAGAAAACCTAACACCATTAAAATAGCAGTTATTTCTCAAATTTATCTACCAATTCA TCATGGAACAGAAAACCTAACACCATTAAAATGGCAGTTATTTCTCAAATTTATCTACCAATTCA A G SNHG14 Ensembl:ENSG00000224078 lincRNA intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1368254697 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42877,RMVar_hsa_circ_170214 13726 RMVar_ID_13726 Human_SNP_ID_570731184 A-to-I Human chr15 - 25352047 25352044 25352047 GGGGTTACAGGTGCACACCACTACACCTGGCTAATGTTTGTATTTTTAGTAGAGATAAGGGTTTT GGGGTTACAGGTGCACACCACTACACCTGGCT___GTTTGTATTTTTAGTAGAGATAAGGGTTTT CATT C UBE3A Ensembl:ENSG00000114062 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1464682085 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_100889,RMVar_hsa_circ_323788,RMVar_hsa_circ_306052,RMVar_hsa_circ_322041,RMVar_hsa_circ_265812,RMVar_hsa_circ_170219,RMVar_hsa_circ_19339,RMVar_hsa_circ_170218 13727 RMVar_ID_13727 Human_SNP_ID_570735073 A-to-I Human chr15 - 25366425 25366425 25366425 TAAAAGTCACTGGCCCTTTTTATCTGGTTTCTAATAGCCTAGTCTAACCCAGCTTCCAGCATTTT TAAAAGTCACTGGCCCTTTTTATCTGGTTTCTGATAGCCTAGTCTAACCCAGCTTCCAGCATTTT T C UBE3A Ensembl:ENSG00000114062 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs968425108 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18660789 RMVar_hsa_circ_12833,RMVar_hsa_circ_100889,RMVar_hsa_circ_323788,RMVar_hsa_circ_306052,RMVar_hsa_circ_265812,RMVar_hsa_circ_292577,RMVar_hsa_circ_170219,RMVar_hsa_circ_19339,RMVar_hsa_circ_333532,RMVar_hsa_circ_368231,RMVar_hsa_circ_170218,RMVar_hsa_circ_296693,RMVar_hsa_circ_286177,RMVar_hsa_circ_267863,RMVar_hsa_circ_3592,RMVar_hsa_circ_170221,RMVar_hsa_circ_170222,RMVar_hsa_circ_170220,RMVar_hsa_circ_170224,RMVar_hsa_circ_371981,RMVar_hsa_circ_359126,RMVar_hsa_circ_360674,RMVar_hsa_circ_347755 13728 RMVar_ID_13728 Human_SNP_ID_570735074 A-to-I Human chr15 - 25366425 25366425 25366425 TAAAAGTCACTGGCCCTTTTTATCTGGTTTCTAATAGCCTAGTCTAACCCAGCTTCCAGCATTTT TAAAAGTCACTGGCCCTTTTTATCTGGTTTCTCATAGCCTAGTCTAACCCAGCTTCCAGCATTTT T G UBE3A Ensembl:ENSG00000114062 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs968425108 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18660789 RMVar_hsa_circ_12833,RMVar_hsa_circ_100889,RMVar_hsa_circ_323788,RMVar_hsa_circ_306052,RMVar_hsa_circ_265812,RMVar_hsa_circ_292577,RMVar_hsa_circ_170219,RMVar_hsa_circ_19339,RMVar_hsa_circ_333532,RMVar_hsa_circ_368231,RMVar_hsa_circ_170218,RMVar_hsa_circ_296693,RMVar_hsa_circ_286177,RMVar_hsa_circ_267863,RMVar_hsa_circ_3592,RMVar_hsa_circ_170221,RMVar_hsa_circ_170222,RMVar_hsa_circ_170220,RMVar_hsa_circ_170224,RMVar_hsa_circ_371981,RMVar_hsa_circ_359126,RMVar_hsa_circ_360674,RMVar_hsa_circ_347755 13729 RMVar_ID_13729 Human_SNP_ID_570737120 A-to-I Human chr15 - 25373588 25373588 25373588 TCTGTAGTCCCAGCTACTTGGGAGGCTGAGGTAGGAGAATCGTTTGAACCCGGGAGGCAGAAGTT TCTGTAGTCCCAGCTACTTGGGAGGCTGAGGTGGGAGAATCGTTTGAACCCGGGAGGCAGAAGTT T C UBE3A Ensembl:ENSG00000114062 Protein coding intron GSE107867 ASD brains,cerebellum;ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs7180183 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12833,RMVar_hsa_circ_100889,RMVar_hsa_circ_323788,RMVar_hsa_circ_306052,RMVar_hsa_circ_265812,RMVar_hsa_circ_292577,RMVar_hsa_circ_170219,RMVar_hsa_circ_19339,RMVar_hsa_circ_333532,RMVar_hsa_circ_170218,RMVar_hsa_circ_296693,RMVar_hsa_circ_286177,RMVar_hsa_circ_267863,RMVar_hsa_circ_3592,RMVar_hsa_circ_170221,RMVar_hsa_circ_170222,RMVar_hsa_circ_170220,RMVar_hsa_circ_170224,RMVar_hsa_circ_371981,RMVar_hsa_circ_359126,RMVar_hsa_circ_360674,RMVar_hsa_circ_170228,RMVar_hsa_circ_312249,RMVar_hsa_circ_369021,RMVar_hsa_circ_321870,RMVar_hsa_circ_293298,RMVar_hsa_circ_170227 13730 RMVar_ID_13730 Human_SNP_ID_570737834 A-to-I Human chr15 - 25376464 25376464 25376464 TTTTAAAAAAGTTTGTAGAGAGTAGCCTCACTATGTTGCCCAGGCTGGTGTTGACCTCCTGGGCT TTTTAAAAAAGTTTGTAGAGAGTAGCCTCACTGTGTTGCCCAGGCTGGTGTTGACCTCCTGGGCT T C UBE3A Ensembl:ENSG00000114062 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs983584015 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12482352 RMVar_hsa_circ_12833,RMVar_hsa_circ_100889,RMVar_hsa_circ_323788,RMVar_hsa_circ_306052,RMVar_hsa_circ_265812,RMVar_hsa_circ_170219,RMVar_hsa_circ_333532,RMVar_hsa_circ_170218,RMVar_hsa_circ_296693,RMVar_hsa_circ_286177,RMVar_hsa_circ_267863,RMVar_hsa_circ_3592,RMVar_hsa_circ_170221,RMVar_hsa_circ_170220,RMVar_hsa_circ_170224,RMVar_hsa_circ_371981,RMVar_hsa_circ_359126,RMVar_hsa_circ_170228,RMVar_hsa_circ_369021,RMVar_hsa_circ_321870,RMVar_hsa_circ_293298,RMVar_hsa_circ_14194,RMVar_hsa_circ_300529,RMVar_hsa_circ_302472,RMVar_hsa_circ_366356 13731 RMVar_ID_13731 Human_SNP_ID_570740527 A-to-I Human chr15 + 25387504 25387504 25387504 AGATCGAGCCACTGCACTCCAGCCTGGGCGACAAAGCGAGACTCCATCTCAAAAAAAAAAGAAAA AGATCGAGCCACTGCACTCCAGCCTGGGCGACCAAGCGAGACTCCATCTCAAAAAAAAAAGAAAA A C SNHG14 Ensembl:ENSG00000224078 lincRNA intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs905868061 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42877 13732 RMVar_ID_13732 Human_SNP_ID_570744710 A-to-I Human chr15 - 25403748 25403748 25403748 ATCCTTTTTCAGGCTGAATAATGTTTTATTGTATGTATATACCACATTTTGCTTATCCATTTACC ATCCTTTTTCAGGCTGAATAATGTTTTATTGTGTGTATATACCACATTTTGCTTATCCATTTACC T C UBE3A Ensembl:ENSG00000114062 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,cerebellum - 29129909,30559470 RNA-Seq:(High) rs942620956 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12833,RMVar_hsa_circ_100889,RMVar_hsa_circ_323788,RMVar_hsa_circ_306052,RMVar_hsa_circ_265812,RMVar_hsa_circ_170219,RMVar_hsa_circ_333532,RMVar_hsa_circ_170218,RMVar_hsa_circ_296693,RMVar_hsa_circ_286177,RMVar_hsa_circ_267863,RMVar_hsa_circ_80104,RMVar_hsa_circ_3592,RMVar_hsa_circ_170221,RMVar_hsa_circ_170220,RMVar_hsa_circ_170224,RMVar_hsa_circ_371981,RMVar_hsa_circ_359126,RMVar_hsa_circ_170228,RMVar_hsa_circ_369021,RMVar_hsa_circ_321870,RMVar_hsa_circ_293298,RMVar_hsa_circ_14194,RMVar_hsa_circ_300529,RMVar_hsa_circ_302472,RMVar_hsa_circ_366356,RMVar_hsa_circ_320320,RMVar_hsa_circ_334080,RMVar_hsa_circ_291022,RMVar_hsa_circ_170230,RMVar_hsa_circ_170231 13733 RMVar_ID_13733 Human_SNP_ID_570753423 A-to-I Human chr15 - 25437381 25437381 25437381 TTACCTGTCAGAGACACAAAGGTACCCAATCAATCTTGTTGAATAAATTGGACAAGTGGGATAAG TTACCTGTCAGAGACACAAAGGTACCCAATCAGTCTTGTTGAATAAATTGGACAAGTGGGATAAG T C UBE3A Ensembl:ENSG00000114062 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs528095011 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17563162 RMVar_hsa_circ_84565,RMVar_hsa_circ_170238 13734 RMVar_ID_13734 Human_SNP_ID_570753425 A-to-I Human chr15 - 25437385 25437385 25437385 AAAGTTACCTGTCAGAGACACAAAGGTACCCAATCAATCTTGTTGAATAAATTGGACAAGTGGGA AAAGTTACCTGTCAGAGACACAAAGGTACCCAGTCAATCTTGTTGAATAAATTGGACAAGTGGGA T C UBE3A Ensembl:ENSG00000114062 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs759316004 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17563162 RMVar_hsa_circ_84565,RMVar_hsa_circ_170238 13735 RMVar_ID_13735 Human_SNP_ID_570753426 A-to-I Human chr15 - 25437386 25437386 25437386 GAAAGTTACCTGTCAGAGACACAAAGGTACCCAATCAATCTTGTTGAATAAATTGGACAAGTGGG GAAAGTTACCTGTCAGAGACACAAAGGTACCCCATCAATCTTGTTGAATAAATTGGACAAGTGGG T G UBE3A Ensembl:ENSG00000114062 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1555437402 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17563162 RMVar_hsa_circ_84565,RMVar_hsa_circ_170238 13736 RMVar_ID_13736 Human_SNP_ID_570753427 A-to-I Human chr15 - 25437395 25437395 25437395 ACAACTGTTGAAAGTTACCTGTCAGAGACACAAAGGTACCCAATCAATCTTGTTGAATAAATTGG ACAACTGTTGAAAGTTACCTGTCAGAGACACAGAGGTACCCAATCAATCTTGTTGAATAAATTGG T C UBE3A Ensembl:ENSG00000114062 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1398300074 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17563162 RMVar_hsa_circ_84565,RMVar_hsa_circ_170238 13737 RMVar_ID_13737 Human_SNP_ID_570855569 A-to-I Human chr15 - 25835946 25835946 25835946 AGCCGGCCGTGGTGGCAGGCACCTGTGGTCCCAGCTACTCGGGAGGCTGAGGCGGGAGAATGGCG AGCCGGCCGTGGTGGCAGGCACCTGTGGTCCCGGCTACTCGGGAGGCTGAGGCGGGAGAATGGCG T C ATP10A Ensembl:ENSG00000206190 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1274656687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_125336 13738 RMVar_ID_13738 Human_SNP_ID_571063021 A-to-I Human chr15 - 26645608 26645608 26645608 TTACCAGGAGTAGAACCATTAAGCTGGTCCAGACAAGTTGGACTCCACCATTTCAACTTCCAGCT TTACCAGGAGTAGAACCATTAAGCTGGTCCAGTCAAGTTGGACTCCACCATTTCAACTTCCAGCT T A GABRB3 Ensembl:ENSG00000166206 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs113017984 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105877,RMVar_hsa_circ_170261 13739 RMVar_ID_13739 Human_SNP_ID_571063022 A-to-I Human chr15 - 26645608 26645608 26645608 TTACCAGGAGTAGAACCATTAAGCTGGTCCAGACAAGTTGGACTCCACCATTTCAACTTCCAGCT TTACCAGGAGTAGAACCATTAAGCTGGTCCAGGCAAGTTGGACTCCACCATTTCAACTTCCAGCT T C GABRB3 Ensembl:ENSG00000166206 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs113017984 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105877,RMVar_hsa_circ_170261 13740 RMVar_ID_13740 Human_SNP_ID_571121775 A-to-I Human chr15 + 26867015 26867015 26867015 CCCTGCGCCCTCCCCCTCCGCCCAGCTCGGCCAAGGGCGCATTTGCTGAGCGTCTGGCGGCCTCT CCCTGCGCCCTCCCCCTCCGCCCAGCTCGGCCGAGGGCGCATTTGCTGAGCGTCTGGCGGCCTCT A G GABRA5 Ensembl:ENSG00000186297 Protein coding 5'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs25410 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1573473,Human_Splice_Rec_1573491,Human_Splice_Rec_1573511 13741 RMVar_ID_13741 Human_SNP_ID_571427540 A-to-I Human chr15 - 28119592 28119592 28119592 AAAATTAGCCTTGTGTGGTGGTGGGTGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGG AAAATTAGCCTTGTGTGGTGGTGGGTGCCTGTGGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGG T C HERC2 Ensembl:ENSG00000128731 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1415158609 Functional Loss SNV dbSNP153 33..33 33 - - - 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 13742 RMVar_ID_13742 Human_SNP_ID_571443855 A-to-I Human chr15 - 28183288 28183288 28183288 GAAGGATTGCTTGAGCCTGGGAGGTTGAAGCTACAGTGAACCGGGATTATGCCACTGTATTCCAG GAAGGATTGCTTGAGCCTGGGAGGTTGAAGCTGCAGTGAACCGGGATTATGCCACTGTATTCCAG T C HERC2 Ensembl:ENSG00000128731 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs776192627 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87685,RMVar_hsa_circ_94513,RMVar_hsa_circ_170285,RMVar_hsa_circ_102114,RMVar_hsa_circ_170287,RMVar_hsa_circ_106541,RMVar_hsa_circ_170288,RMVar_hsa_circ_170289,RMVar_hsa_circ_81015,RMVar_hsa_circ_110247,RMVar_hsa_circ_116835,RMVar_hsa_circ_100452,RMVar_hsa_circ_81630,RMVar_hsa_circ_170292,RMVar_hsa_circ_170294,RMVar_hsa_circ_170295,RMVar_hsa_circ_170293,RMVar_hsa_circ_170297,RMVar_hsa_circ_13771,RMVar_hsa_circ_89074,RMVar_hsa_circ_92364,RMVar_hsa_circ_170299,RMVar_hsa_circ_109327,RMVar_hsa_circ_266242,RMVar_hsa_circ_314620,RMVar_hsa_circ_170300,RMVar_hsa_circ_90373,RMVar_hsa_circ_170302,RMVar_hsa_circ_6160,RMVar_hsa_circ_170301,RMVar_hsa_circ_87491,RMVar_hsa_circ_104393,RMVar_hsa_circ_170307,RMVar_hsa_circ_94296,RMVar_hsa_circ_109270,RMVar_hsa_circ_125821,RMVar_hsa_circ_170308,RMVar_hsa_circ_170309,RMVar_hsa_circ_170311,RMVar_hsa_circ_116251,RMVar_hsa_circ_170312,RMVar_hsa_circ_170313,RMVar_hsa_circ_121229,RMVar_hsa_circ_170316 13743 RMVar_ID_13743 Human_SNP_ID_571443871 A-to-I Human chr15 - 28183350 28183350 28183350 CAAAAATTAGCTGGGCATGATGGTGCAGGCCTATAGTGCCAGCTGTTCGGGAGGCTGAGGTGGAA CAAAAATTAGCTGGGCATGATGGTGCAGGCCTGTAGTGCCAGCTGTTCGGGAGGCTGAGGTGGAA T C HERC2 Ensembl:ENSG00000128731 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1266830980 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87685,RMVar_hsa_circ_94513,RMVar_hsa_circ_170285,RMVar_hsa_circ_102114,RMVar_hsa_circ_170287,RMVar_hsa_circ_106541,RMVar_hsa_circ_170288,RMVar_hsa_circ_170289,RMVar_hsa_circ_81015,RMVar_hsa_circ_110247,RMVar_hsa_circ_116835,RMVar_hsa_circ_100452,RMVar_hsa_circ_81630,RMVar_hsa_circ_170292,RMVar_hsa_circ_170294,RMVar_hsa_circ_170295,RMVar_hsa_circ_170293,RMVar_hsa_circ_170297,RMVar_hsa_circ_13771,RMVar_hsa_circ_89074,RMVar_hsa_circ_92364,RMVar_hsa_circ_170299,RMVar_hsa_circ_109327,RMVar_hsa_circ_266242,RMVar_hsa_circ_314620,RMVar_hsa_circ_170300,RMVar_hsa_circ_90373,RMVar_hsa_circ_170302,RMVar_hsa_circ_6160,RMVar_hsa_circ_170301,RMVar_hsa_circ_87491,RMVar_hsa_circ_104393,RMVar_hsa_circ_170307,RMVar_hsa_circ_94296,RMVar_hsa_circ_109270,RMVar_hsa_circ_125821,RMVar_hsa_circ_170308,RMVar_hsa_circ_170309,RMVar_hsa_circ_170311,RMVar_hsa_circ_116251,RMVar_hsa_circ_170312,RMVar_hsa_circ_170313,RMVar_hsa_circ_121229,RMVar_hsa_circ_170316 13744 RMVar_ID_13744 Human_SNP_ID_571481823 A-to-I Human chr15 - 28319473 28319473 28319473 GCAAGTGATTCTCCCGCCTCAGCCTTCCGAGTAGCTGGGATTACAAGTGTGTGCCACCATGCATG GCAAGTGATTCTCCCGCCTCAGCCTTCCGAGTGGCTGGGATTACAAGTGTGTGCCACCATGCATG T C HERC2 Ensembl:ENSG00000128731 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1464279066 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109209,RMVar_hsa_circ_170326,RMVar_hsa_circ_124945,RMVar_hsa_circ_170350,RMVar_hsa_circ_121230,RMVar_hsa_circ_170374 13745 RMVar_ID_13745 Human_SNP_ID_571542191 A-to-I Human chr15 + 28637451 28637451 28637451 CTGGTTAACTTTGCAGACTCATCAAGAACAGGACCGTTCTTACAAGGAGGTCTGCGCTCCTGTCA CTGGTTAACTTTGCAGACTCATCAAGAACAGGGCCGTTCTTACAAGGAGGTCTGCGCTCCTGTCA A G HERC2P9 Ensembl:ENSG00000206149 Pseudogene exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1211293947 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5567375,Human_RBP_ID_8251300,Human_RBP_ID_18529249,Human_RBP_ID_22355832 Human_Splice_Rec_1574546,Human_Splice_Rec_1574606,Human_Splice_Rec_1574622 RMVar_hsa_circ_10378,RMVar_hsa_circ_53701,RMVar_hsa_circ_66425,RMVar_hsa_circ_365024,RMVar_hsa_circ_170390 13746 RMVar_ID_13746 Human_SNP_ID_571573326 A-to-I Human chr15 + 28753781 28753781 28753781 GGGAGGCTGAGGCAGGAGAATCGCTTGAACCCAGGAGGCGGAAGTTGCAGTGAGCCGAGATCATG GGGAGGCTGAGGCAGGAGAATCGCTTGAACCCCGGAGGCGGAAGTTGCAGTGAGCCGAGATCATG A C WHAMMP2 Ensembl:ENSG00000248334 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs890002869 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269774 13747 RMVar_ID_13747 Human_SNP_ID_571573327 A-to-I Human chr15 + 28753781 28753781 28753781 GGGAGGCTGAGGCAGGAGAATCGCTTGAACCCAGGAGGCGGAAGTTGCAGTGAGCCGAGATCATG GGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGGGAGGCGGAAGTTGCAGTGAGCCGAGATCATG A G WHAMMP2 Ensembl:ENSG00000248334 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs890002869 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269774 13748 RMVar_ID_13748 Human_SNP_ID_571821526 A-to-I Human chr15 - 29706788 29706788 29706788 GGGCATGGTGGCAGACGCCTGTAATCCTAGCTACTCAGAAGCTGAGGCAGGAAAATTGCTTGAAC GGGCATGGTGGCAGACGCCTGTAATCCTAGCTGCTCAGAAGCTGAGGCAGGAAAATTGCTTGAAC T C TJP1 Ensembl:ENSG00000104067 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs933145881 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112878,RMVar_hsa_circ_121459,RMVar_hsa_circ_373698,RMVar_hsa_circ_170408,RMVar_hsa_circ_170407,RMVar_hsa_circ_170411 13749 RMVar_ID_13749 Human_SNP_ID_267941103 A-to-I Human chr6 + 15251129 15251129 15251129 TGTCTTCCGGGTTCAATCGATTCTCCTGTCTCAGCCTCCCGAGTAGGTGGGATTACAGGCACCCC TGTCTTCCGGGTTCAATCGATTCTCCTGTCTCCGCCTCCCGAGTAGGTGGGATTACAGGCACCCC A C JARID2 Ensembl:ENSG00000008083 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1163169005 Functional Loss SNV dbSNP153 33..33 33 - - - 13750 RMVar_ID_13750 Human_SNP_ID_267951495 A-to-I Human chr6 + 15286292 15286292 15286292 TTTTTTTTTTTGAGATGAAGTCTCACTTTGTCACCCGAGTTGGAGTGCAGTGGTGTGATCTCGGC TTTTTTTTTTTGAGATGAAGTCTCACTTTGTCGCCCGAGTTGGAGTGCAGTGGTGTGATCTCGGC A G JARID2 Ensembl:ENSG00000008083 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560129506 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17576224 13751 RMVar_ID_13751 Human_SNP_ID_267952781 A-to-I Human chr6 + 15290802 15290802 15290802 CGCCACGCCCAGTTAATTTTTTTTGTATTTTTAGTAGAGATGAGGTTTCACCATGTTAGCCAGTA CGCCACGCCCAGTTAATTTTTTTTGTATTTTTGGTAGAGATGAGGTTTCACCATGTTAGCCAGTA A G JARID2 Ensembl:ENSG00000008083 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1395328821 Functional Loss SNV dbSNP153 33..33 33 - - - 13752 RMVar_ID_13752 Human_SNP_ID_267957504 A-to-I Human chr6 + 15307423 15307423 15307423 TTTTGTATTTTTAGTAGAGATGGGGTTTTGCCATGTTGCCCAGGCTGGTCTCAGACGACATCAGG TTTTGTATTTTTAGTAGAGATGGGGTTTTGCCGTGTTGCCCAGGCTGGTCTCAGACGACATCAGG A G JARID2 Ensembl:ENSG00000008083 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355647617 Functional Loss SNV dbSNP153 33..33 33 - - - 13753 RMVar_ID_13753 Human_SNP_ID_267960283 A-to-I Human chr6 + 15318149 15318149 15318149 GGAGAATCACTTGAAACCTGGAGGCGGAGGTTACAGTGAATCGAGAACCCTGCCACTGCACTGCA GGAGAATCACTTGAAACCTGGAGGCGGAGGTTGCAGTGAATCGAGAACCCTGCCACTGCACTGCA A G JARID2 Ensembl:ENSG00000008083 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934879448 Functional Loss SNV dbSNP153 33..33 33 - - - 13754 RMVar_ID_13754 Human_SNP_ID_268018275 A-to-I Human chr6 + 15515091 15515091 15515091 TGTTTGTTTGAGACAGTCTTGCTCTGTTGCCTAGGATGGAATGCGTGCTGTGATCCTGTCTCACT TGTTTGTTTGAGACAGTCTTGCTCTGTTGCCTGGGATGGAATGCGTGCTGTGATCCTGTCTCACT A G JARID2 Ensembl:ENSG00000008083 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1190820724 Functional Loss SNV dbSNP153 33..33 33 - - - 13755 RMVar_ID_13755 Human_SNP_ID_268230523 A-to-I Human chr6 - 16350895 16350895 16350895 TATTATTTTGTAGAGACAGGCCTCACTTTGTTACCCAGGCTGGTCTCGAATTCCTGGCCTCACAT TATTATTTTGTAGAGACAGGCCTCACTTTGTTTCCCAGGCTGGTCTCGAATTCCTGGCCTCACAT T A ATXN1 Ensembl:ENSG00000124788 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1199259004 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 13756 RMVar_ID_13756 Human_SNP_ID_268239752 A-to-I Human chr6 - 16391018 16391018 16391018 AGCTGGGATTACAGACGTGTGCTCCTACGCCCAGCTAATTTTTTATATTTTTAGTAGAGATGGGG AGCTGGGATTACAGACGTGTGCTCCTACGCCCGGCTAATTTTTTATATTTTTAGTAGAGATGGGG T C ATXN1 Ensembl:ENSG00000124788 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041195706 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 13757 RMVar_ID_13757 Human_SNP_ID_268240116 A-to-I Human chr6 - 16392558 16392558 16392558 CTAGAAGGCGGAGGTTGCAGGGAGCCAAGATTACACCGCTTCACTCCAACCTGGGCTATAGAGCA CTAGAAGGCGGAGGTTGCAGGGAGCCAAGATTGCACCGCTTCACTCCAACCTGGGCTATAGAGCA T C ATXN1 Ensembl:ENSG00000124788 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971525939 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 13758 RMVar_ID_13758 Human_SNP_ID_268295252 A-to-I Human chr6 - 16619389 16619389 16619389 TGTAATTTCCATCCATAATCTATTTATCTAGCATTTAATTTTCCAGATATTGTGCTATCGTTTAG TGTAATTTCCATCCATAATCTATTTATCTAGCGTTTAATTTTCCAGATATTGTGCTATCGTTTAG T C ATXN1 Ensembl:ENSG00000124788 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1009935271 Functional Loss SNV dbSNP153 33..33 33 - - - 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_320476,RMVar_hsa_circ_298367,RMVar_hsa_circ_310121,RMVar_hsa_circ_282080,RMVar_hsa_circ_237284,RMVar_hsa_circ_288351,RMVar_hsa_circ_333338,RMVar_hsa_circ_286349,RMVar_hsa_circ_290159,RMVar_hsa_circ_237285,RMVar_hsa_circ_237286,RMVar_hsa_circ_312360,RMVar_hsa_circ_237287,RMVar_hsa_circ_237290,RMVar_hsa_circ_286494,RMVar_hsa_circ_237289 13759 RMVar_ID_13759 Human_SNP_ID_268295255 A-to-I Human chr6 - 16619392 16619392 16619392 TACTGTAATTTCCATCCATAATCTATTTATCTAGCATTTAATTTTCCAGATATTGTGCTATCGTT TACTGTAATTTCCATCCATAATCTATTTATCTGGCATTTAATTTTCCAGATATTGTGCTATCGTT T C ATXN1 Ensembl:ENSG00000124788 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1213435594 Functional Loss SNV dbSNP153 33..33 33 - - - 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_320476,RMVar_hsa_circ_298367,RMVar_hsa_circ_310121,RMVar_hsa_circ_282080,RMVar_hsa_circ_237284,RMVar_hsa_circ_288351,RMVar_hsa_circ_333338,RMVar_hsa_circ_286349,RMVar_hsa_circ_290159,RMVar_hsa_circ_237285,RMVar_hsa_circ_237286,RMVar_hsa_circ_312360,RMVar_hsa_circ_237287,RMVar_hsa_circ_237290,RMVar_hsa_circ_286494,RMVar_hsa_circ_237289 13760 RMVar_ID_13760 Human_SNP_ID_268308669 A-to-I Human chr6 - 16675698 16675698 16675698 TATATTTTTTTTAGTAGAGATGGGGCTTCACCATGTCAGTCAGACTGGTCTTGAACTCCTGACCT TATATTTTTTTTAGTAGAGATGGGGCTTCACCGTGTCAGTCAGACTGGTCTTGAACTCCTGACCT T C ATXN1 Ensembl:ENSG00000124788 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs964816866 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_370406,RMVar_hsa_circ_114859,RMVar_hsa_circ_100366,RMVar_hsa_circ_237278,RMVar_hsa_circ_237279,RMVar_hsa_circ_298367,RMVar_hsa_circ_310121,RMVar_hsa_circ_237284,RMVar_hsa_circ_333338,RMVar_hsa_circ_286349,RMVar_hsa_circ_290159,RMVar_hsa_circ_237285,RMVar_hsa_circ_237286,RMVar_hsa_circ_312360,RMVar_hsa_circ_237290,RMVar_hsa_circ_237295,RMVar_hsa_circ_276240,RMVar_hsa_circ_276505,RMVar_hsa_circ_237296,RMVar_hsa_circ_237294 13761 RMVar_ID_13761 Human_SNP_ID_268319885 A-to-I Human chr6 - 16722693 16722693 16722693 GTAAAGCCAATAGAGACTCAGGTTTGATTACTATCATGACTCAGAGACTTTATAATTTGACATAT GTAAAGCCAATAGAGACTCAGGTTTGATTACTGTCATGACTCAGAGACTTTATAATTTGACATAT T C ATXN1 Ensembl:ENSG00000124788 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs375970547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15733014 RMVar_hsa_circ_370406,RMVar_hsa_circ_114859,RMVar_hsa_circ_100366,RMVar_hsa_circ_237278,RMVar_hsa_circ_237279,RMVar_hsa_circ_298367,RMVar_hsa_circ_310121,RMVar_hsa_circ_237284,RMVar_hsa_circ_333338,RMVar_hsa_circ_286349,RMVar_hsa_circ_290159,RMVar_hsa_circ_237285,RMVar_hsa_circ_237286,RMVar_hsa_circ_312360,RMVar_hsa_circ_237290,RMVar_hsa_circ_237295,RMVar_hsa_circ_276240,RMVar_hsa_circ_276505,RMVar_hsa_circ_237296,RMVar_hsa_circ_237294 13762 RMVar_ID_13762 Human_SNP_ID_268495912 A-to-I Human chr6 + 17436223 17436223 17436223 TTCGGTCACTGCAACCTCTGCCTCCTAGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCAAATAAC TTCGGTCACTGCAACCTCTGCCTCCTAGGTTCCAGTGATTCTCCTGCCTCAGCCTCCCAAATAAC A C CAP2 Ensembl:ENSG00000112186 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1160107169 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78210,RMVar_hsa_circ_304022,RMVar_hsa_circ_237308,RMVar_hsa_circ_237309 13763 RMVar_ID_13763 Human_SNP_ID_268501964 A-to-I Human chr6 + 17461285 17461285 17461285 TCTGTCACCCAGTCTGAAGTCTGAAGCGCAGTAGCACAATCTCGGCTCACTGCAGCCTCTGCCAC TCTGTCACCCAGTCTGAAGTCTGAAGCGCAGTGGCACAATCTCGGCTCACTGCAGCCTCTGCCAC A G CAP2 Ensembl:ENSG00000112186 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1178508436 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_237311,RMVar_hsa_circ_78210,RMVar_hsa_circ_304022,RMVar_hsa_circ_237308,RMVar_hsa_circ_237309,RMVar_hsa_circ_237310 13764 RMVar_ID_13764 Human_SNP_ID_268501981 A-to-I Human chr6 + 17461366 17461366 17461366 CTCCTGCCTCAGCCTCCCAAATAGCTGGGACTACAGGCATGCACCACCATGCATGGGTAATTTTT CTCCTGCCTCAGCCTCCCAAATAGCTGGGACTGCAGGCATGCACCACCATGCATGGGTAATTTTT A G CAP2 Ensembl:ENSG00000112186 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049377337 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_237311,RMVar_hsa_circ_78210,RMVar_hsa_circ_304022,RMVar_hsa_circ_237308,RMVar_hsa_circ_237309,RMVar_hsa_circ_237310 13765 RMVar_ID_13765 Human_SNP_ID_268513785 A-to-I Human chr6 + 17511654 17511654 17511654 TTTTGCATTTTTAGTGGAGACGGAGTTTCGCCATGTTGGTCAGGCTGGTCTCAAACTCCTAACCG TTTTGCATTTTTAGTGGAGACGGAGTTTCGCCGTGTTGGTCAGGCTGGTCTCAAACTCCTAACCG A G CAP2 Ensembl:ENSG00000112186 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1030534706 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78210,RMVar_hsa_circ_237309,RMVar_hsa_circ_288983,RMVar_hsa_circ_237313,RMVar_hsa_circ_354064,RMVar_hsa_circ_237314,RMVar_hsa_circ_367312,RMVar_hsa_circ_347946,RMVar_hsa_circ_268600,RMVar_hsa_circ_272760,RMVar_hsa_circ_237316,RMVar_hsa_circ_44561,RMVar_hsa_circ_68380 13766 RMVar_ID_13766 Human_SNP_ID_268541252 A-to-I Human chr6 - 17617660 17617660 17617660 TGAAAAATTTTTTATAGAGATAGGATCTCGCCATGTTGCCTAGGTTGTTCTCAAACTCCTGGGCT TGAAAAATTTTTTATAGAGATAGGATCTCGCCGTGTTGCCTAGGTTGTTCTCAAACTCCTGGGCT T C NUP153 Ensembl:ENSG00000124789 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs931776848 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89488,RMVar_hsa_circ_99553,RMVar_hsa_circ_90664,RMVar_hsa_circ_49410,RMVar_hsa_circ_107175,RMVar_hsa_circ_237327,RMVar_hsa_circ_237328,RMVar_hsa_circ_237326,RMVar_hsa_circ_59559,RMVar_hsa_circ_237329 13767 RMVar_ID_13767 Human_SNP_ID_268542572 A-to-I Human chr6 - 17622193 17622193 17622193 CACCCACCTCAGCCTCCTAAAGTGCTAGGATTACAGGCGTGAGCTACTGTGCCCAGCCAAGATGT CACCCACCTCAGCCTCCTAAAGTGCTAGGATTGCAGGCGTGAGCTACTGTGCCCAGCCAAGATGT T C NUP153 Ensembl:ENSG00000124789 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1422236359 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25987500 RMVar_hsa_circ_89488,RMVar_hsa_circ_99553,RMVar_hsa_circ_90664,RMVar_hsa_circ_49410,RMVar_hsa_circ_107175,RMVar_hsa_circ_237327,RMVar_hsa_circ_237328,RMVar_hsa_circ_237326,RMVar_hsa_circ_59559,RMVar_hsa_circ_237329 13768 RMVar_ID_13768 Human_SNP_ID_268546416 A-to-I Human chr6 - 17635464 17635464 17635464 TCGGGAGGTAGAGGTTGCAGTTACCTGAGATCATGCTACTGCGCTTCAGCCTGGGTGACAGAGTG TCGGGAGGTAGAGGTTGCAGTTACCTGAGATCGTGCTACTGCGCTTCAGCCTGGGTGACAGAGTG T C NUP153 Ensembl:ENSG00000124789 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1054405401 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10312579,Human_RBP_ID_26045031 RMVar_hsa_circ_89488,RMVar_hsa_circ_99553,RMVar_hsa_circ_90664,RMVar_hsa_circ_23490,RMVar_hsa_circ_107175,RMVar_hsa_circ_237327,RMVar_hsa_circ_237328,RMVar_hsa_circ_237326,RMVar_hsa_circ_310009,RMVar_hsa_circ_325316,RMVar_hsa_circ_369938,RMVar_hsa_circ_237329,RMVar_hsa_circ_316109,RMVar_hsa_circ_85113,RMVar_hsa_circ_55604,RMVar_hsa_circ_4149,RMVar_hsa_circ_237332,RMVar_hsa_circ_237333,RMVar_hsa_circ_237331,RMVar_hsa_circ_65871,RMVar_hsa_circ_21184,RMVar_hsa_circ_344538,RMVar_hsa_circ_287957,RMVar_hsa_circ_237334,RMVar_hsa_circ_269249,RMVar_hsa_circ_305235,RMVar_hsa_circ_345015,RMVar_hsa_circ_371686,RMVar_hsa_circ_332223,RMVar_hsa_circ_304881,RMVar_hsa_circ_85331,RMVar_hsa_circ_237338,RMVar_hsa_circ_237340,RMVar_hsa_circ_237341,RMVar_hsa_circ_237339,RMVar_hsa_circ_237337 13769 RMVar_ID_13769 Human_SNP_ID_268546611 A-to-I Human chr6 - 17636248 17636248 17636248 TCACTGAGACCTCCATCTCCCAGATGCATGCAATTCTTGTGCCTCAGCCTCTCAAGTAGCTGGAA TCACTGAGACCTCCATCTCCCAGATGCATGCAGTTCTTGTGCCTCAGCCTCTCAAGTAGCTGGAA T C NUP153 Ensembl:ENSG00000124789 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs895285780 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89488,RMVar_hsa_circ_99553,RMVar_hsa_circ_90664,RMVar_hsa_circ_23490,RMVar_hsa_circ_107175,RMVar_hsa_circ_237327,RMVar_hsa_circ_237328,RMVar_hsa_circ_237326,RMVar_hsa_circ_310009,RMVar_hsa_circ_325316,RMVar_hsa_circ_369938,RMVar_hsa_circ_237329,RMVar_hsa_circ_316109,RMVar_hsa_circ_85113,RMVar_hsa_circ_55604,RMVar_hsa_circ_4149,RMVar_hsa_circ_237332,RMVar_hsa_circ_237333,RMVar_hsa_circ_237331,RMVar_hsa_circ_65871,RMVar_hsa_circ_21184,RMVar_hsa_circ_344538,RMVar_hsa_circ_287957,RMVar_hsa_circ_237334,RMVar_hsa_circ_269249,RMVar_hsa_circ_305235,RMVar_hsa_circ_345015,RMVar_hsa_circ_371686,RMVar_hsa_circ_332223,RMVar_hsa_circ_304881,RMVar_hsa_circ_85331,RMVar_hsa_circ_237338,RMVar_hsa_circ_237340,RMVar_hsa_circ_237341,RMVar_hsa_circ_237339,RMVar_hsa_circ_237337 13770 RMVar_ID_13770 Human_SNP_ID_268549016 A-to-I Human chr6 - 17645180 17645180 17645180 GGAGTGCAATGGCACGGTCTTGGCTCACTGCAACCTCTGCCTCCCGAATTCAAACGATTTCTCCT GGAGTGCAATGGCACGGTCTTGGCTCACTGCAGCCTCTGCCTCCCGAATTCAAACGATTTCTCCT T C NUP153 Ensembl:ENSG00000124789 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900942610 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15747933 RMVar_hsa_circ_237343,RMVar_hsa_circ_89488,RMVar_hsa_circ_90664,RMVar_hsa_circ_23490,RMVar_hsa_circ_107175,RMVar_hsa_circ_237327,RMVar_hsa_circ_237328,RMVar_hsa_circ_310009,RMVar_hsa_circ_325316,RMVar_hsa_circ_369938,RMVar_hsa_circ_237329,RMVar_hsa_circ_85113,RMVar_hsa_circ_4149,RMVar_hsa_circ_237332,RMVar_hsa_circ_237333,RMVar_hsa_circ_237331,RMVar_hsa_circ_65871,RMVar_hsa_circ_21184,RMVar_hsa_circ_344538,RMVar_hsa_circ_305235,RMVar_hsa_circ_345015,RMVar_hsa_circ_371686,RMVar_hsa_circ_332223,RMVar_hsa_circ_85331,RMVar_hsa_circ_79193,RMVar_hsa_circ_237338,RMVar_hsa_circ_237340,RMVar_hsa_circ_237341,RMVar_hsa_circ_237339,RMVar_hsa_circ_101411,RMVar_hsa_circ_371685,RMVar_hsa_circ_374059,RMVar_hsa_circ_336863,RMVar_hsa_circ_125868,RMVar_hsa_circ_92171,RMVar_hsa_circ_237345,RMVar_hsa_circ_237347,RMVar_hsa_circ_237348,RMVar_hsa_circ_237346,RMVar_hsa_circ_237344,RMVar_hsa_circ_237350,RMVar_hsa_circ_74255,RMVar_hsa_circ_357353,RMVar_hsa_circ_237342,RMVar_hsa_circ_332597,RMVar_hsa_circ_74009 13771 RMVar_ID_13771 Human_SNP_ID_268549107 A-to-I Human chr6 - 17645408 17645408 17645408 GAGCCTGTAGTCCCAGCTACCTGGGATGCTGAAGTGGGAGGATTGCTTGAGCCCAGGAATTCAAG GAGCCTGTAGTCCCAGCTACCTGGGATGCTGATGTGGGAGGATTGCTTGAGCCCAGGAATTCAAG T A NUP153 Ensembl:ENSG00000124789 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs945036870 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17576232 RMVar_hsa_circ_237343,RMVar_hsa_circ_89488,RMVar_hsa_circ_90664,RMVar_hsa_circ_23490,RMVar_hsa_circ_107175,RMVar_hsa_circ_237327,RMVar_hsa_circ_237328,RMVar_hsa_circ_310009,RMVar_hsa_circ_325316,RMVar_hsa_circ_369938,RMVar_hsa_circ_237329,RMVar_hsa_circ_85113,RMVar_hsa_circ_4149,RMVar_hsa_circ_237332,RMVar_hsa_circ_237333,RMVar_hsa_circ_237331,RMVar_hsa_circ_65871,RMVar_hsa_circ_21184,RMVar_hsa_circ_344538,RMVar_hsa_circ_305235,RMVar_hsa_circ_345015,RMVar_hsa_circ_371686,RMVar_hsa_circ_332223,RMVar_hsa_circ_85331,RMVar_hsa_circ_79193,RMVar_hsa_circ_237338,RMVar_hsa_circ_237340,RMVar_hsa_circ_237341,RMVar_hsa_circ_237339,RMVar_hsa_circ_101411,RMVar_hsa_circ_371685,RMVar_hsa_circ_374059,RMVar_hsa_circ_336863,RMVar_hsa_circ_125868,RMVar_hsa_circ_92171,RMVar_hsa_circ_237345,RMVar_hsa_circ_237347,RMVar_hsa_circ_237348,RMVar_hsa_circ_237346,RMVar_hsa_circ_237344,RMVar_hsa_circ_237350,RMVar_hsa_circ_74255,RMVar_hsa_circ_357353,RMVar_hsa_circ_237342,RMVar_hsa_circ_332597,RMVar_hsa_circ_74009 13772 RMVar_ID_13772 Human_SNP_ID_268551621 A-to-I Human chr6 - 17654390 17654390 17654390 TTGAAACCAGAAGGCAGAGGTTGCAGTGAGCCAAGATCGCACCACTGCAGTCCGGCCCGGGCAAC TTGAAACCAGAAGGCAGAGGTTGCAGTGAGCCCAGATCGCACCACTGCAGTCCGGCCCGGGCAAC T G NUP153 Ensembl:ENSG00000124789 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs369145316 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15748426 RMVar_hsa_circ_237343,RMVar_hsa_circ_89488,RMVar_hsa_circ_90664,RMVar_hsa_circ_23490,RMVar_hsa_circ_107175,RMVar_hsa_circ_237327,RMVar_hsa_circ_237328,RMVar_hsa_circ_369938,RMVar_hsa_circ_237329,RMVar_hsa_circ_85113,RMVar_hsa_circ_4149,RMVar_hsa_circ_237332,RMVar_hsa_circ_237333,RMVar_hsa_circ_345015,RMVar_hsa_circ_371686,RMVar_hsa_circ_85331,RMVar_hsa_circ_237340,RMVar_hsa_circ_237341,RMVar_hsa_circ_101411,RMVar_hsa_circ_371685,RMVar_hsa_circ_125868,RMVar_hsa_circ_92171,RMVar_hsa_circ_237345,RMVar_hsa_circ_237344,RMVar_hsa_circ_65122,RMVar_hsa_circ_74255,RMVar_hsa_circ_237342,RMVar_hsa_circ_74009,RMVar_hsa_circ_237355,RMVar_hsa_circ_331161,RMVar_hsa_circ_349268,RMVar_hsa_circ_340586,RMVar_hsa_circ_296488,RMVar_hsa_circ_237356,RMVar_hsa_circ_237354,RMVar_hsa_circ_342430,RMVar_hsa_circ_375372,RMVar_hsa_circ_343318,RMVar_hsa_circ_237357,RMVar_hsa_circ_237359,RMVar_hsa_circ_33210,RMVar_hsa_circ_237358,RMVar_hsa_circ_350391,RMVar_hsa_circ_268631 13773 RMVar_ID_13773 Human_SNP_ID_268552087 A-to-I Human chr6 - 17656158 17656158 17656158 CTCTGTCTCCCAGGGTGGAGTGCAGTGGCGCAATCTTGGCTCACTGCAACCTCCACCTCCTGAGT CTCTGTCTCCCAGGGTGGAGTGCAGTGGCGCAGTCTTGGCTCACTGCAACCTCCACCTCCTGAGT T C NUP153 Ensembl:ENSG00000124789 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1455372296 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15748503,Human_RBP_ID_21305225 RMVar_hsa_circ_237343,RMVar_hsa_circ_89488,RMVar_hsa_circ_90664,RMVar_hsa_circ_23490,RMVar_hsa_circ_107175,RMVar_hsa_circ_237327,RMVar_hsa_circ_237328,RMVar_hsa_circ_369938,RMVar_hsa_circ_237329,RMVar_hsa_circ_85113,RMVar_hsa_circ_4149,RMVar_hsa_circ_237332,RMVar_hsa_circ_237333,RMVar_hsa_circ_345015,RMVar_hsa_circ_371686,RMVar_hsa_circ_85331,RMVar_hsa_circ_237340,RMVar_hsa_circ_237341,RMVar_hsa_circ_101411,RMVar_hsa_circ_371685,RMVar_hsa_circ_125868,RMVar_hsa_circ_92171,RMVar_hsa_circ_237345,RMVar_hsa_circ_237344,RMVar_hsa_circ_65122,RMVar_hsa_circ_74255,RMVar_hsa_circ_237342,RMVar_hsa_circ_74009,RMVar_hsa_circ_237355,RMVar_hsa_circ_331161,RMVar_hsa_circ_349268,RMVar_hsa_circ_340586,RMVar_hsa_circ_296488,RMVar_hsa_circ_237356,RMVar_hsa_circ_237354,RMVar_hsa_circ_342430,RMVar_hsa_circ_375372,RMVar_hsa_circ_343318,RMVar_hsa_circ_237357,RMVar_hsa_circ_237359,RMVar_hsa_circ_33210,RMVar_hsa_circ_237358,RMVar_hsa_circ_350391,RMVar_hsa_circ_268631 13774 RMVar_ID_13774 Human_SNP_ID_268552495 A-to-I Human chr6 - 17657464 17657464 17657464 CACCTCCTGAGTTCAAGTGATTCTCATGTCTCAGCCTCCCAAGTAGCTGGGATTACAGGCATGCA CACCTCCTGAGTTCAAGTGATTCTCATGTCTCTGCCTCCCAAGTAGCTGGGATTACAGGCATGCA T A NUP153 Ensembl:ENSG00000124789 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1232047551 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_237343,RMVar_hsa_circ_89488,RMVar_hsa_circ_90664,RMVar_hsa_circ_23490,RMVar_hsa_circ_107175,RMVar_hsa_circ_237327,RMVar_hsa_circ_237328,RMVar_hsa_circ_369938,RMVar_hsa_circ_237329,RMVar_hsa_circ_85113,RMVar_hsa_circ_4149,RMVar_hsa_circ_237332,RMVar_hsa_circ_237333,RMVar_hsa_circ_345015,RMVar_hsa_circ_371686,RMVar_hsa_circ_85331,RMVar_hsa_circ_237340,RMVar_hsa_circ_237341,RMVar_hsa_circ_101411,RMVar_hsa_circ_371685,RMVar_hsa_circ_125868,RMVar_hsa_circ_92171,RMVar_hsa_circ_237345,RMVar_hsa_circ_237344,RMVar_hsa_circ_65122,RMVar_hsa_circ_74255,RMVar_hsa_circ_237342,RMVar_hsa_circ_74009,RMVar_hsa_circ_237355,RMVar_hsa_circ_331161,RMVar_hsa_circ_349268,RMVar_hsa_circ_340586,RMVar_hsa_circ_296488,RMVar_hsa_circ_237356,RMVar_hsa_circ_237354,RMVar_hsa_circ_342430,RMVar_hsa_circ_375372,RMVar_hsa_circ_343318,RMVar_hsa_circ_237357,RMVar_hsa_circ_237359,RMVar_hsa_circ_33210,RMVar_hsa_circ_237358,RMVar_hsa_circ_350391,RMVar_hsa_circ_268631 13775 RMVar_ID_13775 Human_SNP_ID_268552727 A-to-I Human chr6 - 17658344 17658344 17658344 TGGCCCAGGCTGGAGGGCAGTAGCATGATCTCAGCTCACTGCAGCCTCTGCCTCTTGGGTTCAAG TGGCCCAGGCTGGAGGGCAGTAGCATGATCTCGGCTCACTGCAGCCTCTGCCTCTTGGGTTCAAG T C NUP153 Ensembl:ENSG00000124789 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1245788682 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15748635 RMVar_hsa_circ_237343,RMVar_hsa_circ_89488,RMVar_hsa_circ_90664,RMVar_hsa_circ_23490,RMVar_hsa_circ_107175,RMVar_hsa_circ_237327,RMVar_hsa_circ_237328,RMVar_hsa_circ_369938,RMVar_hsa_circ_237329,RMVar_hsa_circ_85113,RMVar_hsa_circ_4149,RMVar_hsa_circ_237332,RMVar_hsa_circ_237333,RMVar_hsa_circ_345015,RMVar_hsa_circ_371686,RMVar_hsa_circ_85331,RMVar_hsa_circ_237340,RMVar_hsa_circ_237341,RMVar_hsa_circ_101411,RMVar_hsa_circ_371685,RMVar_hsa_circ_125868,RMVar_hsa_circ_92171,RMVar_hsa_circ_237345,RMVar_hsa_circ_237344,RMVar_hsa_circ_65122,RMVar_hsa_circ_74255,RMVar_hsa_circ_237342,RMVar_hsa_circ_74009,RMVar_hsa_circ_237355,RMVar_hsa_circ_331161,RMVar_hsa_circ_349268,RMVar_hsa_circ_340586,RMVar_hsa_circ_296488,RMVar_hsa_circ_237356,RMVar_hsa_circ_237354,RMVar_hsa_circ_342430,RMVar_hsa_circ_375372,RMVar_hsa_circ_343318,RMVar_hsa_circ_237357,RMVar_hsa_circ_237359,RMVar_hsa_circ_33210,RMVar_hsa_circ_237358,RMVar_hsa_circ_350391,RMVar_hsa_circ_268631 13776 RMVar_ID_13776 Human_SNP_ID_268553029 A-to-I Human chr6 - 17659530 17659530 17659530 AGGTGGAGGTTGCAGTGAGCCAAGATTGCACCAGTGTACTCCAGCCTGGCAACAGAGCGAGACTT AGGTGGAGGTTGCAGTGAGCCAAGATTGCACCGGTGTACTCCAGCCTGGCAACAGAGCGAGACTT T C NUP153 Ensembl:ENSG00000124789 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1437493496 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10274361,Human_RBP_ID_15748715,Human_RBP_ID_26045088 RMVar_hsa_circ_237343,RMVar_hsa_circ_89488,RMVar_hsa_circ_90664,RMVar_hsa_circ_23490,RMVar_hsa_circ_107175,RMVar_hsa_circ_237327,RMVar_hsa_circ_237328,RMVar_hsa_circ_369938,RMVar_hsa_circ_237329,RMVar_hsa_circ_85113,RMVar_hsa_circ_4149,RMVar_hsa_circ_237332,RMVar_hsa_circ_237333,RMVar_hsa_circ_345015,RMVar_hsa_circ_371686,RMVar_hsa_circ_85331,RMVar_hsa_circ_237340,RMVar_hsa_circ_237341,RMVar_hsa_circ_101411,RMVar_hsa_circ_371685,RMVar_hsa_circ_125868,RMVar_hsa_circ_92171,RMVar_hsa_circ_237345,RMVar_hsa_circ_237344,RMVar_hsa_circ_65122,RMVar_hsa_circ_74255,RMVar_hsa_circ_237342,RMVar_hsa_circ_74009,RMVar_hsa_circ_237355,RMVar_hsa_circ_331161,RMVar_hsa_circ_349268,RMVar_hsa_circ_340586,RMVar_hsa_circ_296488,RMVar_hsa_circ_237356,RMVar_hsa_circ_237354,RMVar_hsa_circ_342430,RMVar_hsa_circ_375372,RMVar_hsa_circ_343318,RMVar_hsa_circ_237357,RMVar_hsa_circ_237359,RMVar_hsa_circ_33210,RMVar_hsa_circ_237358,RMVar_hsa_circ_350391,RMVar_hsa_circ_268631 13777 RMVar_ID_13777 Human_SNP_ID_268554174 A-to-I Human chr6 - 17663507 17663507 17663507 ATAATCCCAGTGCTTTGAGAGGCTCAGGCAGAAGGATCACTTGAGTCCAGGAATTCAAGACTAGC ATAATCCCAGTGCTTTGAGAGGCTCAGGCAGAGGGATCACTTGAGTCCAGGAATTCAAGACTAGC T C NUP153 Ensembl:ENSG00000124789 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs918971304 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15748932,Human_RBP_ID_24150306 RMVar_hsa_circ_237343,RMVar_hsa_circ_89488,RMVar_hsa_circ_90664,RMVar_hsa_circ_107175,RMVar_hsa_circ_237327,RMVar_hsa_circ_237328,RMVar_hsa_circ_369938,RMVar_hsa_circ_237329,RMVar_hsa_circ_85113,RMVar_hsa_circ_237332,RMVar_hsa_circ_237333,RMVar_hsa_circ_371686,RMVar_hsa_circ_85331,RMVar_hsa_circ_237340,RMVar_hsa_circ_237341,RMVar_hsa_circ_101411,RMVar_hsa_circ_371685,RMVar_hsa_circ_125868,RMVar_hsa_circ_92171,RMVar_hsa_circ_237345,RMVar_hsa_circ_237344,RMVar_hsa_circ_65122,RMVar_hsa_circ_237342,RMVar_hsa_circ_74009,RMVar_hsa_circ_237355,RMVar_hsa_circ_331161,RMVar_hsa_circ_349268,RMVar_hsa_circ_296488,RMVar_hsa_circ_237356,RMVar_hsa_circ_237354,RMVar_hsa_circ_342430,RMVar_hsa_circ_375372,RMVar_hsa_circ_343318,RMVar_hsa_circ_237357,RMVar_hsa_circ_237359,RMVar_hsa_circ_33210,RMVar_hsa_circ_237358,RMVar_hsa_circ_237366,RMVar_hsa_circ_335064,RMVar_hsa_circ_350391,RMVar_hsa_circ_268631,RMVar_hsa_circ_347788,RMVar_hsa_circ_289306,RMVar_hsa_circ_290470,RMVar_hsa_circ_270860,RMVar_hsa_circ_237364,RMVar_hsa_circ_237365,RMVar_hsa_circ_237363,RMVar_hsa_circ_237367,RMVar_hsa_circ_74825,RMVar_hsa_circ_357202,RMVar_hsa_circ_374151,RMVar_hsa_circ_89983,RMVar_hsa_circ_237368 13778 RMVar_ID_13778 Human_SNP_ID_268555054 A-to-I Human chr6 - 17666467 17666467 17666467 CTCTGTCTCCCAGGCTGGAGTGCGGTGGCACAATCTCGGCCCATTGAAAGCTCTGCCTCCGGGTT CTCTGTCTCCCAGGCTGGAGTGCGGTGGCACAGTCTCGGCCCATTGAAAGCTCTGCCTCCGGGTT T C NUP153 Ensembl:ENSG00000124789 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1345974088 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15749046 RMVar_hsa_circ_237343,RMVar_hsa_circ_90664,RMVar_hsa_circ_237328,RMVar_hsa_circ_85113,RMVar_hsa_circ_237333,RMVar_hsa_circ_371686,RMVar_hsa_circ_85331,RMVar_hsa_circ_237340,RMVar_hsa_circ_237341,RMVar_hsa_circ_371685,RMVar_hsa_circ_125868,RMVar_hsa_circ_92171,RMVar_hsa_circ_237344,RMVar_hsa_circ_65122,RMVar_hsa_circ_237342,RMVar_hsa_circ_237355,RMVar_hsa_circ_331161,RMVar_hsa_circ_296488,RMVar_hsa_circ_237356,RMVar_hsa_circ_342430,RMVar_hsa_circ_375372,RMVar_hsa_circ_237357,RMVar_hsa_circ_33210,RMVar_hsa_circ_237358,RMVar_hsa_circ_237366,RMVar_hsa_circ_335064,RMVar_hsa_circ_268631,RMVar_hsa_circ_347788,RMVar_hsa_circ_289306,RMVar_hsa_circ_270860,RMVar_hsa_circ_237364,RMVar_hsa_circ_237365,RMVar_hsa_circ_237369,RMVar_hsa_circ_79694,RMVar_hsa_circ_74825,RMVar_hsa_circ_357202,RMVar_hsa_circ_89983,RMVar_hsa_circ_237368,RMVar_hsa_circ_276501,RMVar_hsa_circ_295614,RMVar_hsa_circ_352693,RMVar_hsa_circ_282111,RMVar_hsa_circ_84627,RMVar_hsa_circ_237371,RMVar_hsa_circ_237373,RMVar_hsa_circ_237374,RMVar_hsa_circ_237372,RMVar_hsa_circ_237370 13779 RMVar_ID_13779 Human_SNP_ID_268555536 A-to-I Human chr6 - 17668213 17668213 17668213 AAATTAGCCAGGTGTGGCGGTGCGCACCTGTAATCTCAGCTACTCCGGAGGCTGAGGCAGGAGAA AAATTAGCCAGGTGTGGCGGTGCGCACCTGTAGTCTCAGCTACTCCGGAGGCTGAGGCAGGAGAA T C NUP153 Ensembl:ENSG00000124789 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs539765181 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_237343,RMVar_hsa_circ_90664,RMVar_hsa_circ_237328,RMVar_hsa_circ_85113,RMVar_hsa_circ_237333,RMVar_hsa_circ_371686,RMVar_hsa_circ_85331,RMVar_hsa_circ_237340,RMVar_hsa_circ_237341,RMVar_hsa_circ_371685,RMVar_hsa_circ_125868,RMVar_hsa_circ_92171,RMVar_hsa_circ_237344,RMVar_hsa_circ_65122,RMVar_hsa_circ_237342,RMVar_hsa_circ_237355,RMVar_hsa_circ_331161,RMVar_hsa_circ_296488,RMVar_hsa_circ_237356,RMVar_hsa_circ_342430,RMVar_hsa_circ_375372,RMVar_hsa_circ_237357,RMVar_hsa_circ_33210,RMVar_hsa_circ_237358,RMVar_hsa_circ_237366,RMVar_hsa_circ_335064,RMVar_hsa_circ_268631,RMVar_hsa_circ_347788,RMVar_hsa_circ_289306,RMVar_hsa_circ_270860,RMVar_hsa_circ_237364,RMVar_hsa_circ_237365,RMVar_hsa_circ_237369,RMVar_hsa_circ_79694,RMVar_hsa_circ_74825,RMVar_hsa_circ_357202,RMVar_hsa_circ_89983,RMVar_hsa_circ_237368,RMVar_hsa_circ_276501,RMVar_hsa_circ_295614,RMVar_hsa_circ_352693,RMVar_hsa_circ_282111,RMVar_hsa_circ_84627,RMVar_hsa_circ_237371,RMVar_hsa_circ_237373,RMVar_hsa_circ_237374,RMVar_hsa_circ_237372,RMVar_hsa_circ_237370 13780 RMVar_ID_13780 Human_SNP_ID_268555580 A-to-I Human chr6 - 17668352 17668352 17668352 TGATCGGCCAGGTGCGGTGGCTTACGCCTGTAATCCTAGCACTTTGGGAGGCCCAGGCCAGTGGA TGATCGGCCAGGTGCGGTGGCTTACGCCTGTATTCCTAGCACTTTGGGAGGCCCAGGCCAGTGGA T A NUP153 Ensembl:ENSG00000124789 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs938990083 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_237343,RMVar_hsa_circ_90664,RMVar_hsa_circ_237328,RMVar_hsa_circ_85113,RMVar_hsa_circ_237333,RMVar_hsa_circ_371686,RMVar_hsa_circ_85331,RMVar_hsa_circ_237340,RMVar_hsa_circ_237341,RMVar_hsa_circ_371685,RMVar_hsa_circ_125868,RMVar_hsa_circ_92171,RMVar_hsa_circ_237344,RMVar_hsa_circ_65122,RMVar_hsa_circ_237342,RMVar_hsa_circ_237355,RMVar_hsa_circ_331161,RMVar_hsa_circ_296488,RMVar_hsa_circ_237356,RMVar_hsa_circ_342430,RMVar_hsa_circ_375372,RMVar_hsa_circ_237357,RMVar_hsa_circ_33210,RMVar_hsa_circ_237358,RMVar_hsa_circ_237366,RMVar_hsa_circ_335064,RMVar_hsa_circ_268631,RMVar_hsa_circ_347788,RMVar_hsa_circ_289306,RMVar_hsa_circ_270860,RMVar_hsa_circ_237364,RMVar_hsa_circ_237365,RMVar_hsa_circ_237369,RMVar_hsa_circ_79694,RMVar_hsa_circ_74825,RMVar_hsa_circ_357202,RMVar_hsa_circ_89983,RMVar_hsa_circ_237368,RMVar_hsa_circ_276501,RMVar_hsa_circ_295614,RMVar_hsa_circ_352693,RMVar_hsa_circ_282111,RMVar_hsa_circ_84627,RMVar_hsa_circ_237371,RMVar_hsa_circ_237373,RMVar_hsa_circ_237374,RMVar_hsa_circ_237372,RMVar_hsa_circ_237370 13781 RMVar_ID_13781 Human_SNP_ID_268555682 A-to-I Human chr6 - 17668730 17668730 17668730 CAAGCGATTCTCGTGCCCCAGCCTCCCTAGTAACTGAGATTACAGGCACGTGCCATCATGCCCTG CAAGCGATTCTCGTGCCCCAGCCTCCCTAGTATCTGAGATTACAGGCACGTGCCATCATGCCCTG T A NUP153 Ensembl:ENSG00000124789 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1309148519 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_237343,RMVar_hsa_circ_90664,RMVar_hsa_circ_237328,RMVar_hsa_circ_85113,RMVar_hsa_circ_237333,RMVar_hsa_circ_371686,RMVar_hsa_circ_85331,RMVar_hsa_circ_237340,RMVar_hsa_circ_237341,RMVar_hsa_circ_371685,RMVar_hsa_circ_125868,RMVar_hsa_circ_92171,RMVar_hsa_circ_237344,RMVar_hsa_circ_65122,RMVar_hsa_circ_237342,RMVar_hsa_circ_237355,RMVar_hsa_circ_331161,RMVar_hsa_circ_296488,RMVar_hsa_circ_237356,RMVar_hsa_circ_342430,RMVar_hsa_circ_375372,RMVar_hsa_circ_237357,RMVar_hsa_circ_33210,RMVar_hsa_circ_237358,RMVar_hsa_circ_237366,RMVar_hsa_circ_335064,RMVar_hsa_circ_268631,RMVar_hsa_circ_347788,RMVar_hsa_circ_289306,RMVar_hsa_circ_270860,RMVar_hsa_circ_237364,RMVar_hsa_circ_237365,RMVar_hsa_circ_237369,RMVar_hsa_circ_79694,RMVar_hsa_circ_74825,RMVar_hsa_circ_357202,RMVar_hsa_circ_89983,RMVar_hsa_circ_237368,RMVar_hsa_circ_276501,RMVar_hsa_circ_295614,RMVar_hsa_circ_352693,RMVar_hsa_circ_282111,RMVar_hsa_circ_84627,RMVar_hsa_circ_237371,RMVar_hsa_circ_237373,RMVar_hsa_circ_237374,RMVar_hsa_circ_237372,RMVar_hsa_circ_237370 13782 RMVar_ID_13782 Human_SNP_ID_268571001 A-to-I Human chr6 - 17721788 17721788 17721788 GGGAGATCTCCTGGGAATACCGGGTGCTGTAGACTTAAAAAAAAAAAATCCGGAGAGAGTTGGCT GGGAGATCTCCTGGGAATACCGGGTGCTGTAGTCTTAAAAAAAAAAAATCCGGAGAGAGTTGGCT T A RNA5SP204 Ensembl:ENSG00000201415 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1252151314 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252821,Human_RBP_ID_270907,Human_RBP_ID_284806,Human_RBP_ID_792437,Human_RBP_ID_1045697,Human_RBP_ID_1142297,Human_RBP_ID_4905348,Human_RBP_ID_5219112,Human_RBP_ID_5276920,Human_RBP_ID_5428105,Human_RBP_ID_5450780,Human_RBP_ID_5477661,Human_RBP_ID_5510915,Human_RBP_ID_7578462,Human_RBP_ID_8140767,Human_RBP_ID_8638697,Human_RBP_ID_8906181,Human_RBP_ID_9192262,Human_RBP_ID_9263099,Human_RBP_ID_9308010,Human_RBP_ID_9341631,Human_RBP_ID_9438731,Human_RBP_ID_15750343,Human_RBP_ID_17041480,Human_RBP_ID_17305784,Human_RBP_ID_17709990,Human_RBP_ID_18070282,Human_RBP_ID_18202470,Human_RBP_ID_18210916,Human_RBP_ID_18368947,Human_RBP_ID_18449865,Human_RBP_ID_21947076,Human_RBP_ID_21992141,Human_RBP_ID_22366461,Human_RBP_ID_22424035,Human_RBP_ID_22513657,Human_RBP_ID_22746527,Human_RBP_ID_22830147,Human_RBP_ID_23110726,Human_RBP_ID_23120453,Human_RBP_ID_23137836,Human_RBP_ID_23293696,Human_RBP_ID_24548854,Human_RBP_ID_24562892,Human_RBP_ID_26041088,Human_RBP_ID_26751334,Human_RBP_ID_27102662,Human_RBP_ID_27160848,Human_RBP_ID_27343438,Human_RBP_ID_27521484 13783 RMVar_ID_13783 Human_SNP_ID_268571002 A-to-I Human chr6 - 17721788 17721788 17721788 GGGAGATCTCCTGGGAATACCGGGTGCTGTAGACTTAAAAAAAAAAAATCCGGAGAGAGTTGGCT GGGAGATCTCCTGGGAATACCGGGTGCTGTAGCCTTAAAAAAAAAAAATCCGGAGAGAGTTGGCT T G RNA5SP204 Ensembl:ENSG00000201415 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1252151314 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252821,Human_RBP_ID_270907,Human_RBP_ID_284806,Human_RBP_ID_792437,Human_RBP_ID_1045697,Human_RBP_ID_1142297,Human_RBP_ID_4905348,Human_RBP_ID_5219112,Human_RBP_ID_5276920,Human_RBP_ID_5428105,Human_RBP_ID_5450780,Human_RBP_ID_5477661,Human_RBP_ID_5510915,Human_RBP_ID_7578462,Human_RBP_ID_8140767,Human_RBP_ID_8638697,Human_RBP_ID_8906181,Human_RBP_ID_9192262,Human_RBP_ID_9263099,Human_RBP_ID_9308010,Human_RBP_ID_9341631,Human_RBP_ID_9438731,Human_RBP_ID_15750343,Human_RBP_ID_17041480,Human_RBP_ID_17305784,Human_RBP_ID_17709990,Human_RBP_ID_18070282,Human_RBP_ID_18202470,Human_RBP_ID_18210916,Human_RBP_ID_18368947,Human_RBP_ID_18449865,Human_RBP_ID_21947076,Human_RBP_ID_21992141,Human_RBP_ID_22366461,Human_RBP_ID_22424035,Human_RBP_ID_22513657,Human_RBP_ID_22746527,Human_RBP_ID_22830147,Human_RBP_ID_23110726,Human_RBP_ID_23120453,Human_RBP_ID_23137836,Human_RBP_ID_23293696,Human_RBP_ID_24548854,Human_RBP_ID_24562892,Human_RBP_ID_26041088,Human_RBP_ID_26751334,Human_RBP_ID_27102662,Human_RBP_ID_27160848,Human_RBP_ID_27343438,Human_RBP_ID_27521484 13784 RMVar_ID_13784 Human_SNP_ID_268583182 A-to-I Human chr6 - 17757063 17757063 17757063 TACTCTCGTGTAGGCTGGAGTGCAGCAGCGCAATCTCAGCCTCACTGCAACTTCTGCCCCCAGGG TACTCTCGTGTAGGCTGGAGTGCAGCAGCGCAGTCTCAGCCTCACTGCAACTTCTGCCCCCAGGG T C RF00017-4531,RF00017-4495 RNACentral:URS000098F531,RNACentral:URS0000923EDC SRP RNA,SRP RNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1448520367 Functional Loss SNV dbSNP153 33..33 33 - - - 13785 RMVar_ID_13785 Human_SNP_ID_268584968 A-to-I Human chr6 - 17763348 17763348 17763348 CTCCTGCCTCAGCCTCCCGTGTAGCTGGGACTACAGGCACGTGCCAGCACATCTGGCTAATTTTT CTCCTGCCTCAGCCTCCCGTGTAGCTGGGACTGCAGGCACGTGCCAGCACATCTGGCTAATTTTT T C KIF13A Ensembl:ENSG00000137177 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444868069 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96596,RMVar_hsa_circ_237386 13786 RMVar_ID_13786 Human_SNP_ID_268588606 A-to-I Human chr6 - 17778016 17778016 17778016 GTAGTGCCTCAGCCTCCCAGATAGCTGGAACCACAGGCACCCACCACCATGCCCAGCTAATTTTT GTAGTGCCTCAGCCTCCCAGATAGCTGGAACCCCAGGCACCCACCACCATGCCCAGCTAATTTTT T G KIF13A Ensembl:ENSG00000137177 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1371027103 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2764,RMVar_hsa_circ_50918,RMVar_hsa_circ_124411,RMVar_hsa_circ_13908,RMVar_hsa_circ_44419,RMVar_hsa_circ_69679,RMVar_hsa_circ_95328,RMVar_hsa_circ_237389,RMVar_hsa_circ_349342,RMVar_hsa_circ_237390,RMVar_hsa_circ_266299,RMVar_hsa_circ_277575,RMVar_hsa_circ_61774,RMVar_hsa_circ_237392,RMVar_hsa_circ_20403,RMVar_hsa_circ_237393,RMVar_hsa_circ_343139,RMVar_hsa_circ_94917,RMVar_hsa_circ_121386,RMVar_hsa_circ_40137,RMVar_hsa_circ_274493,RMVar_hsa_circ_320855,RMVar_hsa_circ_125285,RMVar_hsa_circ_110489,RMVar_hsa_circ_237396,RMVar_hsa_circ_78477,RMVar_hsa_circ_237398,RMVar_hsa_circ_237399,RMVar_hsa_circ_237400,RMVar_hsa_circ_237397,RMVar_hsa_circ_237395 13787 RMVar_ID_13787 Human_SNP_ID_268592593 A-to-I Human chr6 - 17793695 17793694 17793696 TTGCCCACACTGGTCTCAAATTCCTGGACTCAAGTGATCCTCCTGCCTCAGCCTCCCAAAGTGTA TTGCCCACACTGGTCTCAAATTCCTGGACTC__GTGATCCTCCTGCCTCAGCCTCCCAAAGTGTA CTT C KIF13A Ensembl:ENSG00000137177 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1369612202 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_2764,RMVar_hsa_circ_50918,RMVar_hsa_circ_61774,RMVar_hsa_circ_121386,RMVar_hsa_circ_110489,RMVar_hsa_circ_237396,RMVar_hsa_circ_78477,RMVar_hsa_circ_237397,RMVar_hsa_circ_86443,RMVar_hsa_circ_237395,RMVar_hsa_circ_24608,RMVar_hsa_circ_120005,RMVar_hsa_circ_106632,RMVar_hsa_circ_237401,RMVar_hsa_circ_95460,RMVar_hsa_circ_237403,RMVar_hsa_circ_59803,RMVar_hsa_circ_237404,RMVar_hsa_circ_32664,RMVar_hsa_circ_102798,RMVar_hsa_circ_237406,RMVar_hsa_circ_237408,RMVar_hsa_circ_237407,RMVar_hsa_circ_55655,RMVar_hsa_circ_356889 13788 RMVar_ID_13788 Human_SNP_ID_268592601 A-to-I Human chr6 - 17793710 17793710 17793710 GGGCATGTCATTCTGTTGCCCACACTGGTCTCAAATTCCTGGACTCAAGTGATCCTCCTGCCTCA GGGCATGTCATTCTGTTGCCCACACTGGTCTCGAATTCCTGGACTCAAGTGATCCTCCTGCCTCA T C KIF13A Ensembl:ENSG00000137177 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1450128996 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2764,RMVar_hsa_circ_50918,RMVar_hsa_circ_61774,RMVar_hsa_circ_121386,RMVar_hsa_circ_110489,RMVar_hsa_circ_237396,RMVar_hsa_circ_78477,RMVar_hsa_circ_237397,RMVar_hsa_circ_86443,RMVar_hsa_circ_237395,RMVar_hsa_circ_24608,RMVar_hsa_circ_120005,RMVar_hsa_circ_106632,RMVar_hsa_circ_237401,RMVar_hsa_circ_95460,RMVar_hsa_circ_237403,RMVar_hsa_circ_59803,RMVar_hsa_circ_237404,RMVar_hsa_circ_32664,RMVar_hsa_circ_102798,RMVar_hsa_circ_237406,RMVar_hsa_circ_237408,RMVar_hsa_circ_237407,RMVar_hsa_circ_55655,RMVar_hsa_circ_356889 13789 RMVar_ID_13789 Human_SNP_ID_268593537 A-to-I Human chr6 - 17797127 17797127 17797127 TACTCGGGAGGCTGAGGCAGGAGAATGGCGTGAACCTGAGAGGTGGAGCTTGTAGTGAGCGGAGA TACTCGGGAGGCTGAGGCAGGAGAATGGCGTGCACCTGAGAGGTGGAGCTTGTAGTGAGCGGAGA T G KIF13A Ensembl:ENSG00000137177 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1213753693 Functional Loss SNV dbSNP153 33..33 33 - - - 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_6510,RMVar_hsa_circ_120005,RMVar_hsa_circ_237401,RMVar_hsa_circ_95460,RMVar_hsa_circ_59803,RMVar_hsa_circ_237404,RMVar_hsa_circ_32664,RMVar_hsa_circ_102798,RMVar_hsa_circ_237406,RMVar_hsa_circ_237408,RMVar_hsa_circ_237407,RMVar_hsa_circ_107995,RMVar_hsa_circ_324130,RMVar_hsa_circ_55655,RMVar_hsa_circ_47636,RMVar_hsa_circ_364270,RMVar_hsa_circ_83939,RMVar_hsa_circ_237413,RMVar_hsa_circ_24201,RMVar_hsa_circ_237414,RMVar_hsa_circ_55873 13790 RMVar_ID_13790 Human_SNP_ID_268594310 A-to-I Human chr6 - 17800075 17800075 17800075 GGGCGTCTCCACGTGGAAGTGATGCGTGTTACAGGAGCTGTTCCAGAGCGTGTGGTGGAGGATGA GGGCGTCTCCACGTGGAAGTGATGCGTGTTACGGGAGCTGTTCCAGAGCGTGTGGTGGAGGATGA T C KIF13A Ensembl:ENSG00000137177 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1402700525 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4874463,Human_RBP_ID_8898799 Human_Splice_Rec_740604,Human_Splice_Rec_740704,Human_Splice_Rec_740778,Human_Splice_Rec_740848,Human_Splice_Rec_740922,Human_Splice_Rec_740964 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_6510,RMVar_hsa_circ_120005,RMVar_hsa_circ_237401,RMVar_hsa_circ_95460,RMVar_hsa_circ_59803,RMVar_hsa_circ_237404,RMVar_hsa_circ_32664,RMVar_hsa_circ_102798,RMVar_hsa_circ_237406,RMVar_hsa_circ_237408,RMVar_hsa_circ_237407,RMVar_hsa_circ_107995,RMVar_hsa_circ_324130,RMVar_hsa_circ_55655,RMVar_hsa_circ_47636,RMVar_hsa_circ_364270,RMVar_hsa_circ_83939,RMVar_hsa_circ_237413,RMVar_hsa_circ_24201,RMVar_hsa_circ_237414,RMVar_hsa_circ_55873,RMVar_hsa_circ_76991,RMVar_hsa_circ_30332,RMVar_hsa_circ_100686,RMVar_hsa_circ_360843,RMVar_hsa_circ_45509,RMVar_hsa_circ_237415,RMVar_hsa_circ_237416 13791 RMVar_ID_13791 Human_SNP_ID_268602163 A-to-I Human chr6 - 17829291 17829291 17829291 AGTTTTCCGGAGTCTATGAGACATGTAATGATATTATAGCCCTGAGGGCTAAGGGTTGTATGTTT AGTTTTCCGGAGTCTATGAGACATGTAATGATGTTATAGCCCTGAGGGCTAAGGGTTGTATGTTT T C KIF13A Ensembl:ENSG00000137177 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1195552579 Functional Loss SNV dbSNP153 33..33 33 - - - 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_237423 13792 RMVar_ID_13792 Human_SNP_ID_268602181 A-to-I Human chr6 - 17829370 17829370 17829370 GAGGTCAAAACTACTTTAATATAAACACGAACATGTTGTTTGGCTCTGCTCTCTCATTTTATCAC GAGGTCAAAACTACTTTAATATAAACACGAACGTGTTGTTTGGCTCTGCTCTCTCATTTTATCAC T C KIF13A Ensembl:ENSG00000137177 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1164945424 Functional Loss SNV dbSNP153 33..33 33 - - - 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_237423 13793 RMVar_ID_13793 Human_SNP_ID_268602396 A-to-I Human chr6 - 17830323 17830323 17830323 ACCCTTAGCCCTCAGGGCTATAACATCATTACATGTCTCATAGACTCTGGAAAATTCCACCAATA ACCCTTAGCCCTCAGGGCTATAACATCATTACTTGTCTCATAGACTCTGGAAAATTCCACCAATA T A KIF13A Ensembl:ENSG00000137177 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1178871085 Functional Loss SNV dbSNP153 33..33 33 - - - 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_237423 13794 RMVar_ID_13794 Human_SNP_ID_268602411 A-to-I Human chr6 - 17830364 17830364 17830364 CTAAGACTGAGAACATTTTAAACTACAAACATAAACGTACAACCCTTAGCCCTCAGGGCTATAAC CTAAGACTGAGAACATTTTAAACTACAAACATGAACGTACAACCCTTAGCCCTCAGGGCTATAAC T C KIF13A Ensembl:ENSG00000137177 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1390738728 Functional Loss SNV dbSNP153 33..33 33 - - - 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_237423 13795 RMVar_ID_13795 Human_SNP_ID_268607105 A-to-I Human chr6 - 17848608 17848608 17848608 TGAGCCGAGATTGCTCCCCTGTACTCCAGCCTAGGCAACAGAGCGAGACTCTGTCTCAAAAAAAA TGAGCCGAGATTGCTCCCCTGTACTCCAGCCTGGGCAACAGAGCGAGACTCTGTCTCAAAAAAAA T C KIF13A Ensembl:ENSG00000137177 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1420909015 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7576,RMVar_hsa_circ_61774,RMVar_hsa_circ_110489,RMVar_hsa_circ_86443,RMVar_hsa_circ_237395,RMVar_hsa_circ_237401,RMVar_hsa_circ_102798,RMVar_hsa_circ_237408,RMVar_hsa_circ_100686,RMVar_hsa_circ_237415,RMVar_hsa_circ_377368,RMVar_hsa_circ_65096,RMVar_hsa_circ_71091,RMVar_hsa_circ_64164,RMVar_hsa_circ_17466,RMVar_hsa_circ_9089,RMVar_hsa_circ_323015,RMVar_hsa_circ_237428,RMVar_hsa_circ_341752,RMVar_hsa_circ_70621 13796 RMVar_ID_13796 Human_SNP_ID_268614874 A-to-I Human chr6 - 17880205 17880205 17880205 ATAACTGTAATCCCAGCACTTTGGGAAGCCAAAGCAGGAAGATCACTTGAGGCTAGGAGAATTCG ATAACTGTAATCCCAGCACTTTGGGAAGCCAATGCAGGAAGATCACTTGAGGCTAGGAGAATTCG T A KIF13A Ensembl:ENSG00000137177 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1231885681 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7576,RMVar_hsa_circ_102798,RMVar_hsa_circ_237408,RMVar_hsa_circ_100686,RMVar_hsa_circ_237415 13797 RMVar_ID_13797 Human_SNP_ID_268614952 A-to-I Human chr6 - 17880566 17880566 17880566 TGGAGTGCAATGGTGCGATCTTGGCTCACTGCAACCTCCGCCTCCTGGGTTCAAATGATTCTCCT TGGAGTGCAATGGTGCGATCTTGGCTCACTGCTACCTCCGCCTCCTGGGTTCAAATGATTCTCCT T A KIF13A Ensembl:ENSG00000137177 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1201032614 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7576,RMVar_hsa_circ_102798,RMVar_hsa_circ_237408,RMVar_hsa_circ_100686,RMVar_hsa_circ_237415 13798 RMVar_ID_13798 Human_SNP_ID_268615026 A-to-I Human chr6 - 17880759 17880759 17880759 AAAATTAGACAAGTATGGTGGCATGTGCCTGTAGTCCTAGCTACTCGGGAGGCTGCTTGAGCCCA AAAATTAGACAAGTATGGTGGCATGTGCCTGTGGTCCTAGCTACTCGGGAGGCTGCTTGAGCCCA T C KIF13A Ensembl:ENSG00000137177 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs940176281 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7576,RMVar_hsa_circ_102798,RMVar_hsa_circ_237408,RMVar_hsa_circ_100686,RMVar_hsa_circ_237415 13799 RMVar_ID_13799 Human_SNP_ID_268620871 A-to-I Human chr6 - 17906541 17906541 17906541 GGGAGGCTGAGATGGGAGGATCTCTTGAGCCCAGGAGGTTGAGGCTACAATGAGCTGTCATCACA GGGAGGCTGAGATGGGAGGATCTCTTGAGCCCGGGAGGTTGAGGCTACAATGAGCTGTCATCACA T C KIF13A Ensembl:ENSG00000137177 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1257034226 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7576 13800 RMVar_ID_13800 Human_SNP_ID_268624536 A-to-I Human chr6 - 17921888 17921888 17921888 TAAACTCTGCAGATTTTTTAGTCACTCAACTAATAGGACTTGCAGGAAAAGTGAAATGTCTATAA TAAACTCTGCAGATTTTTTAGTCACTCAACTAGTAGGACTTGCAGGAAAAGTGAAATGTCTATAA T C KIF13A Ensembl:ENSG00000137177 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935971685 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7576 13801 RMVar_ID_13801 Human_SNP_ID_268625551 A-to-I Human chr6 - 17926335 17926335 17926335 CCAGCTACTCGGGAGACTGAGGCACGAGAATCACTTGAACCCAGGAGACAGAAGGTTGCAGTGAG CCAGCTACTCGGGAGACTGAGGCACGAGAATCTCTTGAACCCAGGAGACAGAAGGTTGCAGTGAG T A KIF13A Ensembl:ENSG00000137177 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1194683650 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7576 13802 RMVar_ID_13802 Human_SNP_ID_268628060 A-to-I Human chr6 - 17937172 17937172 17937172 ATTTATGTATGTATGTGTATATATGTATAGACAGGGTCTCACTATGTCGCCCAGGCTAGAGTGCA ATTTATGTATGTATGTGTATATATGTATAGACGGGGTCTCACTATGTCGCCCAGGCTAGAGTGCA T C KIF13A Ensembl:ENSG00000137177 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1296220570 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15751102 RMVar_hsa_circ_7576 13803 RMVar_ID_13803 Human_SNP_ID_268629360 A-to-I Human chr6 - 17942202 17942202 17942202 GACTTCCTGGGCTCAAGTAATCCTCCTACCTCAGCCTCCCGAGTAGCTGGGACTATAGGTGTATG GACTTCCTGGGCTCAAGTAATCCTCCTACCTCGGCCTCCCGAGTAGCTGGGACTATAGGTGTATG T C KIF13A Ensembl:ENSG00000137177 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs34714377 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7576 13804 RMVar_ID_13804 Human_SNP_ID_268630882 A-to-I Human chr6 - 17948648 17948648 17948648 GCTGATGCAGAGAATCGCTTGAACCTGGAGGCAGAGGTCCCAGTGAGCCGAGATCACGCTGCTGC GCTGATGCAGAGAATCGCTTGAACCTGGAGGCCGAGGTCCCAGTGAGCCGAGATCACGCTGCTGC T G KIF13A Ensembl:ENSG00000137177 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs938882904 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7576 13805 RMVar_ID_13805 Human_SNP_ID_268630899 A-to-I Human chr6 - 17948699 17948699 17948699 AAAATTAGCCGGGCATGGTGGTGGGTGCCTGTAATTCCAGTTACTCGGGAGGCTGATGCAGAGAA AAAATTAGCCGGGCATGGTGGTGGGTGCCTGTCATTCCAGTTACTCGGGAGGCTGATGCAGAGAA T G KIF13A Ensembl:ENSG00000137177 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs367544311 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7576 13806 RMVar_ID_13806 Human_SNP_ID_268630915 A-to-I Human chr6 - 17948764 17948764 17948764 GTCAGGAGTTTGAGACCAGCCCAGCCCAGCCAACATGGTGAAACCCCATCTCTACAAAAAATACA GTCAGGAGTTTGAGACCAGCCCAGCCCAGCCATCATGGTGAAACCCCATCTCTACAAAAAATACA T A KIF13A Ensembl:ENSG00000137177 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1561793545 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7576 13807 RMVar_ID_13807 Human_SNP_ID_268637516 A-to-I Human chr6 - 17975087 17975087 17975087 TGCCCTCCTCTTTCTCTCAAAGTTCTGGGATTACAGGTGTGAACCACTGCGCCCAGCTGGGAATG TGCCCTCCTCTTTCTCTCAAAGTTCTGGGATTGCAGGTGTGAACCACTGCGCCCAGCTGGGAATG T C KIF13A Ensembl:ENSG00000137177 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1244352743 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2997083,Human_RBP_ID_17576238 RMVar_hsa_circ_7576 13808 RMVar_ID_13808 Human_SNP_ID_268637624 A-to-I Human chr6 - 17975244 17975244 17975244 GATTCAAACAATTCTCCTGCCTGAGCCTTCCGAGTAGCTGGGATTACAGAAACCTGCCACCCCGC GATTCAAACAATTCTCCTGCCTGAGCCTTCCGGGTAGCTGGGATTACAGAAACCTGCCACCCCGC T C KIF13A Ensembl:ENSG00000137177 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1273260554 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7576 13809 RMVar_ID_13809 Human_SNP_ID_268637653 A-to-I Human chr6 - 17975277 17975277 17975277 ACAGTCTCAGCTCATTGCAACCTTCACCTCCCAGATTCAAACAATTCTCCTGCCTGAGCCTTCCG ACAGTCTCAGCTCATTGCAACCTTCACCTCCCGGATTCAAACAATTCTCCTGCCTGAGCCTTCCG T C KIF13A Ensembl:ENSG00000137177 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1324099338 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7576 13810 RMVar_ID_13810 Human_SNP_ID_268639785 A-to-I Human chr6 - 17981564 17981564 17981564 AAAAAATTAGCCTGGCGTGGTGGTGTGTGACTATAGTCCCAGCTACTCGGGAGGCTGAGGCAGGG AAAAAATTAGCCTGGCGTGGTGGTGTGTGACTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGG T C KIF13A Ensembl:ENSG00000137177 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs774163365 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7576 13811 RMVar_ID_13811 Human_SNP_ID_268639815 A-to-I Human chr6 - 17981701 17981701 17981701 ATAAGGCCGGACACAGTGACTCAGTGACTCACACCTGTAATCCCAGCACTTTGGGAGCCTGAGGC ATAAGGCCGGACACAGTGACTCAGTGACTCACCCCTGTAATCCCAGCACTTTGGGAGCCTGAGGC T G KIF13A Ensembl:ENSG00000137177 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1044039790 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7576 13812 RMVar_ID_13812 Human_SNP_ID_268640335 A-to-I Human chr6 - 17983609 17983609 17983609 ACATACCTATAATCCCAGTTGCCTAGGAGCCTAAGGCAGGAGAATCGCCTGAGCCTTGGCGATGG ACATACCTATAATCCCAGTTGCCTAGGAGCCTGAGGCAGGAGAATCGCCTGAGCCTTGGCGATGG T C KIF13A Ensembl:ENSG00000137177 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1332730205 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7576 13813 RMVar_ID_13813 Human_SNP_ID_268640379 A-to-I Human chr6 - 17983767 17983767 17983767 AAGGTAGTTCTGGGCTGGGTGAGGTAGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTAGGGT AAGGTAGTTCTGGGCTGGGTGAGGTAGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTAGGGT T C KIF13A Ensembl:ENSG00000137177 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1488427933 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15751783 RMVar_hsa_circ_7576 13814 RMVar_ID_13814 Human_SNP_ID_268680416 A-to-I Human chr6 - 18128812 18128812 18128812 GGGAGGCTGAGGCAGGAGAATCACTTGAACCTAGGAGGCGGAGGTTGCAGTGAGCTGAGATCATG GGGAGGCTGAGGCAGGAGAATCACTTGAACCTGGGAGGCGGAGGTTGCAGTGAGCTGAGATCATG T C TPMT Ensembl:ENSG00000137364 Protein coding 3'UTR GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs879193360 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127537,RMVar_hsa_circ_237435,RMVar_hsa_circ_92699,RMVar_hsa_circ_237434 13815 RMVar_ID_13815 Human_SNP_ID_268680433 A-to-I Human chr6 - 18128884 18128884 18128884 AACCCCGTCTCTACTAAAAATACAAAAAAATTAGCCAGGCGTGGTGGCACGTGCCTGTAATCCCA AACCCCGTCTCTACTAAAAATACAAAAAAATTGGCCAGGCGTGGTGGCACGTGCCTGTAATCCCA T C TPMT Ensembl:ENSG00000137364 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1142370 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127537,RMVar_hsa_circ_237435,RMVar_hsa_circ_92699,RMVar_hsa_circ_237434 13816 RMVar_ID_13816 Human_SNP_ID_268680438 A-to-I Human chr6 - 18128890 18128890 18128890 AAAAGCAACCCCGTCTCTACTAAAAATACAAAAAAATTAGCCAGGCGTGGTGGCACGTGCCTGTA AAAAGCAACCCCGTCTCTACTAAAAATACAAACAAATTAGCCAGGCGTGGTGGCACGTGCCTGTA T G TPMT Ensembl:ENSG00000137364 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1025695424 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127537,RMVar_hsa_circ_237435,RMVar_hsa_circ_92699,RMVar_hsa_circ_237434 13817 RMVar_ID_13817 Human_SNP_ID_268680440 A-to-I Human chr6 - 18128895 18128895 18128895 AATAGAAAAGCAACCCCGTCTCTACTAAAAATACAAAAAAATTAGCCAGGCGTGGTGGCACGTGC AATAGAAAAGCAACCCCGTCTCTACTAAAAATTCAAAAAAATTAGCCAGGCGTGGTGGCACGTGC T A TPMT Ensembl:ENSG00000137364 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1142367 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127537,RMVar_hsa_circ_237435,RMVar_hsa_circ_92699,RMVar_hsa_circ_237434 13818 RMVar_ID_13818 Human_SNP_ID_268680441 A-to-I Human chr6 - 18128895 18128895 18128895 AATAGAAAAGCAACCCCGTCTCTACTAAAAATACAAAAAAATTAGCCAGGCGTGGTGGCACGTGC AATAGAAAAGCAACCCCGTCTCTACTAAAAATGCAAAAAAATTAGCCAGGCGTGGTGGCACGTGC T C TPMT Ensembl:ENSG00000137364 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1142367 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127537,RMVar_hsa_circ_237435,RMVar_hsa_circ_92699,RMVar_hsa_circ_237434 13819 RMVar_ID_13819 Human_SNP_ID_268680462 A-to-I Human chr6 - 18128983 18128983 18128983 GCAGTCCTCCTGTCTTGGCCACCCAAAGTGCTAGGATTACAGGTATGAGCCATTGCGCTGGCCCT GCAGTCCTCCTGTCTTGGCCACCCAAAGTGCTGGGATTACAGGTATGAGCCATTGCGCTGGCCCT T C TPMT Ensembl:ENSG00000137364 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs980420759 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_658104 RMVar_hsa_circ_127537,RMVar_hsa_circ_237435,RMVar_hsa_circ_92699,RMVar_hsa_circ_237434 13820 RMVar_ID_13820 Human_SNP_ID_268680699 A-to-I Human chr6 - 18130067 18130067 18130067 GTTGGTCAGGCTGATCTCGAGCTCCTGACCTCAGGTGATCTACCCACCTCGGCCTCCCAAAGTGC GTTGGTCAGGCTGATCTCGAGCTCCTGACCTCGGGTGATCTACCCACCTCGGCCTCCCAAAGTGC T C TPMT Ensembl:ENSG00000137364 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1442613938 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127537,RMVar_hsa_circ_237435,RMVar_hsa_circ_92699,RMVar_hsa_circ_237434 13821 RMVar_ID_13821 Human_SNP_ID_268680744 A-to-I Human chr6 - 18130209 18130209 18130209 GCAATCTCAGCTCACTGCAACCTCTGCCTCCCAGGTTCAGGTGATTCTCCTGCCTCAGCCTCCTG GCAATCTCAGCTCACTGCAACCTCTGCCTCCCGGGTTCAGGTGATTCTCCTGCCTCAGCCTCCTG T C TPMT Ensembl:ENSG00000137364 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1362651682 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1416088,Human_miRNA_ID_2723415 RMVar_hsa_circ_127537,RMVar_hsa_circ_237435,RMVar_hsa_circ_92699,RMVar_hsa_circ_237434 13822 RMVar_ID_13822 Human_SNP_ID_268680748 A-to-I Human chr6 - 18130238 18130238 18130238 TCTTGTTGCCCAACCTGGAGTGCAATGGTGCAATCTCAGCTCACTGCAACCTCTGCCTCCCAGGT TCTTGTTGCCCAACCTGGAGTGCAATGGTGCAGTCTCAGCTCACTGCAACCTCTGCCTCCCAGGT T C TPMT Ensembl:ENSG00000137364 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1142348 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_658116,Human_RBP_ID_15751851 Human_miRNA_ID_686608,Human_miRNA_ID_889174,Human_miRNA_ID_1065786,Human_miRNA_ID_1077112,Human_miRNA_ID_2274920,Human_miRNA_ID_2400807,Human_miRNA_ID_2494741,Human_miRNA_ID_3108702 RMVar_hsa_circ_127537,RMVar_hsa_circ_237435,RMVar_hsa_circ_92699,RMVar_hsa_circ_237434 13823 RMVar_ID_13823 Human_SNP_ID_268680749 A-to-I Human chr6 - 18130238 18130238 18130238 TCTTGTTGCCCAACCTGGAGTGCAATGGTGCAATCTCAGCTCACTGCAACCTCTGCCTCCCAGGT TCTTGTTGCCCAACCTGGAGTGCAATGGTGCACTCTCAGCTCACTGCAACCTCTGCCTCCCAGGT T G TPMT Ensembl:ENSG00000137364 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1142348 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_658116,Human_RBP_ID_15751851 Human_miRNA_ID_686608,Human_miRNA_ID_889174,Human_miRNA_ID_1065786,Human_miRNA_ID_1077112,Human_miRNA_ID_2274920,Human_miRNA_ID_2400807,Human_miRNA_ID_2494741,Human_miRNA_ID_3108702 RMVar_hsa_circ_127537,RMVar_hsa_circ_237435,RMVar_hsa_circ_92699,RMVar_hsa_circ_237434 13824 RMVar_ID_13824 Human_SNP_ID_268680752 A-to-I Human chr6 - 18130246 18130246 18130246 AGTTTCGTTCTTGTTGCCCAACCTGGAGTGCAATGGTGCAATCTCAGCTCACTGCAACCTCTGCC AGTTTCGTTCTTGTTGCCCAACCTGGAGTGCAGTGGTGCAATCTCAGCTCACTGCAACCTCTGCC T C TPMT Ensembl:ENSG00000137364 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1142346 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_658116,Human_RBP_ID_15751851 Human_miRNA_ID_686609,Human_miRNA_ID_889175,Human_miRNA_ID_1065787,Human_miRNA_ID_1077113,Human_miRNA_ID_2274920,Human_miRNA_ID_2400807,Human_miRNA_ID_2494741,Human_miRNA_ID_2500668,Human_miRNA_ID_3108702,Human_miRNA_ID_3110142 RMVar_hsa_circ_127537,RMVar_hsa_circ_237435,RMVar_hsa_circ_92699,RMVar_hsa_circ_237434 13825 RMVar_ID_13825 Human_SNP_ID_268682220 A-to-I Human chr6 - 18136734 18136734 18136734 ACTATCTCGGCTCACCGCAACCTCTGCCTGCCAGGTTCAAGCGAATCTCCTGCCTCAGCCTCCCA ACTATCTCGGCTCACCGCAACCTCTGCCTGCCGGGTTCAAGCGAATCTCCTGCCTCAGCCTCCCA T C TPMT Ensembl:ENSG00000137364 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs760500746 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9131,RMVar_hsa_circ_92699,RMVar_hsa_circ_237434 13826 RMVar_ID_13826 Human_SNP_ID_268683381 A-to-I Human chr6 - 18141480 18141480 18141480 CAAAAATTAGCTGGCTGTGGTGGTGCATACCTATAATCCTAGCTACTCTGGAGGCTGAGGCAGGA CAAAAATTAGCTGGCTGTGGTGGTGCATACCTGTAATCCTAGCTACTCTGGAGGCTGAGGCAGGA T C TPMT Ensembl:ENSG00000137364 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1436168679 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9131,RMVar_hsa_circ_92699,RMVar_hsa_circ_237434,RMVar_hsa_circ_237436,RMVar_hsa_circ_365274 13827 RMVar_ID_13827 Human_SNP_ID_268696624 A-to-I Human chr6 + 18192168 18192168 18192168 CCCATAGTCCTAGCTACTTAGGAGGCTGAGACAGGAGGATGGCCTGAGCTTGGGAGGTCAAGGCT CCCATAGTCCTAGCTACTTAGGAGGCTGAGACGGGAGGATGGCCTGAGCTTGGGAGGTCAAGGCT A G KDM1B Ensembl:ENSG00000165097 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs974806930 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265720,RMVar_hsa_circ_346435,RMVar_hsa_circ_268976,RMVar_hsa_circ_70326,RMVar_hsa_circ_84289,RMVar_hsa_circ_237441,RMVar_hsa_circ_237442,RMVar_hsa_circ_117298,RMVar_hsa_circ_237440,RMVar_hsa_circ_267955,RMVar_hsa_circ_237452,RMVar_hsa_circ_112208,RMVar_hsa_circ_16681,RMVar_hsa_circ_75600,RMVar_hsa_circ_237456,RMVar_hsa_circ_237457,RMVar_hsa_circ_237459,RMVar_hsa_circ_309197,RMVar_hsa_circ_29908,RMVar_hsa_circ_237461,RMVar_hsa_circ_272165,RMVar_hsa_circ_352414,RMVar_hsa_circ_17013,RMVar_hsa_circ_237463,RMVar_hsa_circ_237464 13828 RMVar_ID_13828 Human_SNP_ID_268700519 A-to-I Human chr6 + 18206695 18206695 18206695 GATCCTCCTGCCTCGGCCTCCCAAAATGCTGGAATTACAGGCATGAGCCACTGCACCAGGACTTG GATCCTCCTGCCTCGGCCTCCCAAAATGCTGGGATTACAGGCATGAGCCACTGCACCAGGACTTG A G KDM1B Ensembl:ENSG00000165097 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs933706693 Functional Loss SNV dbSNP153 33..33 33 - - - 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_237457,RMVar_hsa_circ_29908,RMVar_hsa_circ_352414,RMVar_hsa_circ_17013,RMVar_hsa_circ_343368,RMVar_hsa_circ_237464,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_237471,RMVar_hsa_circ_237472,RMVar_hsa_circ_123828,RMVar_hsa_circ_57082,RMVar_hsa_circ_341192 13829 RMVar_ID_13829 Human_SNP_ID_268705151 A-to-I Human chr6 + 18222104 18222104 18222104 GGGGAAAAAACCGTCTCTACATAGTAAAACTGAAATGTTTCTAAGGCGATATGATAATGCAAACC GGGGAAAAAACCGTCTCTACATAGTAAAACTGCAATGTTTCTAAGGCGATATGATAATGCAAACC A C KDM1B Ensembl:ENSG00000165097 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs759063603 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2015562,Human_RBP_ID_17065005 Human_miRNA_ID_2731174 RMVar_hsa_circ_268976,RMVar_hsa_circ_237472,RMVar_hsa_circ_123828,RMVar_hsa_circ_111938,RMVar_hsa_circ_99359,RMVar_hsa_circ_237474,RMVar_hsa_circ_237480 13830 RMVar_ID_13830 Human_SNP_ID_268710685 A-to-I Human chr6 - 18240790 18240790 18240790 CCTGCTTTTAAAAAAAAGAAAATTAGTTTTTTAGAGATAGGGTCTTCTGATTTTGCCCAGGCTGG CCTGCTTTTAAAAAAAAGAAAATTAGTTTTTTGGAGATAGGGTCTTCTGATTTTGCCCAGGCTGG T C DEK Ensembl:ENSG00000124795 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs564135506 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15753177,Human_RBP_ID_18859664,Human_RBP_ID_23058409,Human_RBP_ID_25988825 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 13831 RMVar_ID_13831 Human_SNP_ID_268711060 A-to-I Human chr6 - 18242356 18242356 18242356 CTGCCGTATTATTCTTTCTTCTTTTTTGAGACAGAGTCTTGCTTTGTTGCCCAGGCTGGGGTACA CTGCCGTATTATTCTTTCTTCTTTTTTGAGACGGAGTCTTGCTTTGTTGCCCAGGCTGGGGTACA T C DEK Ensembl:ENSG00000124795 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1484441876 Functional Loss SNV dbSNP153 33..33 33 - - - 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 13832 RMVar_ID_13832 Human_SNP_ID_268711061 A-to-I Human chr6 - 18242360 18242360 18242360 GAGACTGCCGTATTATTCTTTCTTCTTTTTTGAGACAGAGTCTTGCTTTGTTGCCCAGGCTGGGG GAGACTGCCGTATTATTCTTTCTTCTTTTTTGTGACAGAGTCTTGCTTTGTTGCCCAGGCTGGGG T A DEK Ensembl:ENSG00000124795 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs953308387 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7579118,Human_RBP_ID_15753275 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 13833 RMVar_ID_13833 Human_SNP_ID_268713096 A-to-I Human chr6 - 18249706 18249706 18249706 TCTGTCAGATGAATCTAGTAGTGATGAAGATGAAAAGAAAAACAAGGAAGAGTCTTCAGATGATG TCTGTCAGATGAATCTAGTAGTGATGAAGATGTAAAGAAAAACAAGGAAGAGTCTTCAGATGATG T A DEK Ensembl:ENSG00000124795 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs140697635 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_658285,Human_RBP_ID_951565,Human_RBP_ID_1668093,Human_RBP_ID_2015677,Human_RBP_ID_3802577,Human_RBP_ID_7579284,Human_RBP_ID_9192358,Human_RBP_ID_9399997,Human_RBP_ID_10274993,Human_RBP_ID_15753744,Human_RBP_ID_18538951,Human_RBP_ID_18859687,Human_RBP_ID_22830179,Human_RBP_ID_23068603,Human_RBP_ID_24150773,Human_RBP_ID_24548343,Human_RBP_ID_26045231,Human_RBP_ID_26354757,Human_RBP_ID_27092919,Human_RBP_ID_27827346 Human_Splice_Rec_741193,Human_Splice_Rec_741215,Human_Splice_Rec_741233,Human_Splice_Rec_741253,Human_Splice_Rec_741275,Human_Splice_Rec_741293,Human_Splice_Rec_741313,Human_Splice_Rec_741331,Human_Splice_Rec_741343 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 13834 RMVar_ID_13834 Human_SNP_ID_268713097 A-to-I Human chr6 - 18249706 18249706 18249706 TCTGTCAGATGAATCTAGTAGTGATGAAGATGAAAAGAAAAACAAGGAAGAGTCTTCAGATGATG TCTGTCAGATGAATCTAGTAGTGATGAAGATGGAAAGAAAAACAAGGAAGAGTCTTCAGATGATG T C DEK Ensembl:ENSG00000124795 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs140697635 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_658285,Human_RBP_ID_951565,Human_RBP_ID_1668093,Human_RBP_ID_2015677,Human_RBP_ID_3802577,Human_RBP_ID_7579284,Human_RBP_ID_9192358,Human_RBP_ID_9399997,Human_RBP_ID_10274993,Human_RBP_ID_15753744,Human_RBP_ID_18538951,Human_RBP_ID_18859687,Human_RBP_ID_22830179,Human_RBP_ID_23068603,Human_RBP_ID_24150773,Human_RBP_ID_24548343,Human_RBP_ID_26045231,Human_RBP_ID_26354757,Human_RBP_ID_27092919,Human_RBP_ID_27827346 Human_Splice_Rec_741193,Human_Splice_Rec_741215,Human_Splice_Rec_741233,Human_Splice_Rec_741253,Human_Splice_Rec_741275,Human_Splice_Rec_741293,Human_Splice_Rec_741313,Human_Splice_Rec_741331,Human_Splice_Rec_741343 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 13835 RMVar_ID_13835 Human_SNP_ID_268714426 A-to-I Human chr6 - 18254139 18254139 18254139 TTTAATAGAGACGGGGTTTTGCCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATC TTTAATAGAGACGGGGTTTTGCCATGTTGGCCGGGCTGGTCTCGAACTCCTGACCTCAGGTGATC T C DEK Ensembl:ENSG00000124795 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1357558909 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6526,RMVar_hsa_circ_62800,RMVar_hsa_circ_348771,RMVar_hsa_circ_358479,RMVar_hsa_circ_237484,RMVar_hsa_circ_272128,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 13836 RMVar_ID_13836 Human_SNP_ID_269097336 A-to-I Human chr6 - 19800365 19800365 19800365 CAGCTCACTGCAACCTCTGTCTCCCGGATTCAAGTGATTCTCCCACCTCAGCCTCCCAAGTAGCT CAGCTCACTGCAACCTCTGTCTCCCGGATTCATGTGATTCTCCCACCTCAGCCTCCCAAGTAGCT T A LNC-LBCS Ensembl:ENSG00000228412 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs975195906 Functional Loss SNV dbSNP153 33..33 33 - - - 13837 RMVar_ID_13837 Human_SNP_ID_269097337 A-to-I Human chr6 - 19800365 19800365 19800365 CAGCTCACTGCAACCTCTGTCTCCCGGATTCAAGTGATTCTCCCACCTCAGCCTCCCAAGTAGCT CAGCTCACTGCAACCTCTGTCTCCCGGATTCAGGTGATTCTCCCACCTCAGCCTCCCAAGTAGCT T C LNC-LBCS Ensembl:ENSG00000228412 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs975195906 Functional Loss SNV dbSNP153 33..33 33 - - - 13838 RMVar_ID_13838 Human_SNP_ID_269192731 A-to-I Human chr6 - 20186147 20186147 20186147 TGATACAGTCTCACTGTGACCCATGCTGGAGTACAGTGGCACTATCATAGCTTACTGCAGCCTCA TGATACAGTCTCACTGTGACCCATGCTGGAGTGCAGTGGCACTATCATAGCTTACTGCAGCCTCA T C MBOAT1 Ensembl:ENSG00000172197 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1039171602 Functional Loss SNV dbSNP153 33..33 33 - - - 13839 RMVar_ID_13839 Human_SNP_ID_269263544 A-to-I Human chr6 + 20459701 20459701 20459701 AGTTACAGCCAGACTCTTCGTCCCAGCACTTTAGGAGGCCTAGGCGGGCAGATCACTTGAGTCCA AGTTACAGCCAGACTCTTCGTCCCAGCACTTTTGGAGGCCTAGGCGGGCAGATCACTTGAGTCCA A T E2F3 Ensembl:ENSG00000112242 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1380601582 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15758326 13840 RMVar_ID_13840 Human_SNP_ID_269269601 A-to-I Human chr6 + 20485539 20485539 20485539 AGACGGAGGTTGCAGTGAGCTGAGATTGGGCCACTGAACTCCAGCCTGGGTGACAGAGCAAGATT AGACGGAGGTTGCAGTGAGCTGAGATTGGGCCCCTGAACTCCAGCCTGGGTGACAGAGCAAGATT A C E2F3 Ensembl:ENSG00000112242 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1275558650 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26045435 RMVar_hsa_circ_322183,RMVar_hsa_circ_328065,RMVar_hsa_circ_237507 13841 RMVar_ID_13841 Human_SNP_ID_269269762 A-to-I Human chr6 + 20486294 20486291 20486294 CAGAAGGGGAGACATACACATACTTTTTTGAGAAGGAGTCTCGCTCTGTCGCCCAGGCTGGAGTG CAGAAGGGGAGACATACACATACTTTTTTG___AGGAGTCTCGCTCTGTCGCCCAGGCTGGAGTG GAGA G E2F3 Ensembl:ENSG00000112242 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1279198214 Functional Loss DEL dbSNP153 31..33 33 - - - RMVar_hsa_circ_322183,RMVar_hsa_circ_328065,RMVar_hsa_circ_237507 13842 RMVar_ID_13842 Human_SNP_ID_269285553 A-to-I Human chr6 + 20551387 20551387 20551387 CAGTAACTAAAATATCTTTTTTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCACCCAGGCTGGAG CAGTAACTAAAATATCTTTTTTTTTTTTTTTGTGACGGAGTCTCGCTCTGTCACCCAGGCTGGAG A T CDKAL1 Ensembl:ENSG00000145996 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1274502539 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66259,RMVar_hsa_circ_333900,RMVar_hsa_circ_363507,RMVar_hsa_circ_285477,RMVar_hsa_circ_237508,RMVar_hsa_circ_315738,RMVar_hsa_circ_363102 13843 RMVar_ID_13843 Human_SNP_ID_269286096 A-to-I Human chr6 + 20553669 20553663 20553669 GTCTCACTCCGCTGCCCAGGCTGGAGTGCAGTAGCACCATCTCGGCTTACTGCAACCTCTGCCTT GTCTCACTCCGCTGCCCAGGCTGGAGT______GCACCATCTCGGCTTACTGCAACCTCTGCCTT TGCAGTA T CDKAL1 Ensembl:ENSG00000145996 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355627695 Functional Loss DEL dbSNP153 28..33 33 - - - RMVar_hsa_circ_66259,RMVar_hsa_circ_333900,RMVar_hsa_circ_363507,RMVar_hsa_circ_285477,RMVar_hsa_circ_237508,RMVar_hsa_circ_315738,RMVar_hsa_circ_363102 13844 RMVar_ID_13844 Human_SNP_ID_269286099 A-to-I Human chr6 + 20553669 20553669 20553669 GTCTCACTCCGCTGCCCAGGCTGGAGTGCAGTAGCACCATCTCGGCTTACTGCAACCTCTGCCTT GTCTCACTCCGCTGCCCAGGCTGGAGTGCAGTGGCACCATCTCGGCTTACTGCAACCTCTGCCTT A G CDKAL1 Ensembl:ENSG00000145996 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs549792243 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66259,RMVar_hsa_circ_333900,RMVar_hsa_circ_363507,RMVar_hsa_circ_285477,RMVar_hsa_circ_237508,RMVar_hsa_circ_315738,RMVar_hsa_circ_363102 13845 RMVar_ID_13845 Human_SNP_ID_269286478 A-to-I Human chr6 + 20555420 20555420 20555420 TGGGCTTACTGTATCCTCCGCCTCCTGAGTTCAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGC TGGGCTTACTGTATCCTCCGCCTCCTGAGTTCGAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGC A G CDKAL1 Ensembl:ENSG00000145996 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1433921426 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66259,RMVar_hsa_circ_333900,RMVar_hsa_circ_363507,RMVar_hsa_circ_285477,RMVar_hsa_circ_237508,RMVar_hsa_circ_315738,RMVar_hsa_circ_363102 13846 RMVar_ID_13846 Human_SNP_ID_269306568 A-to-I Human chr6 + 20638817 20638817 20638817 CACCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGTCATGATGG CACCATGCCCAGCTAATTTTTGTATTTTTAGTGGAGACGGGGTTTCACCATGTTGGTCATGATGG A G CDKAL1 Ensembl:ENSG00000145996 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031532614 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66259,RMVar_hsa_circ_333900,RMVar_hsa_circ_363507,RMVar_hsa_circ_285477,RMVar_hsa_circ_315738,RMVar_hsa_circ_363102 13847 RMVar_ID_13847 Human_SNP_ID_269306573 A-to-I Human chr6 + 20638834 20638834 20638834 TTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGTCATGATGGTCTCGATCTCTTGACAT TTTTGTATTTTTAGTAGAGACGGGGTTTCACCGTGTTGGTCATGATGGTCTCGATCTCTTGACAT A G CDKAL1 Ensembl:ENSG00000145996 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs919260150 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66259,RMVar_hsa_circ_333900,RMVar_hsa_circ_363507,RMVar_hsa_circ_285477,RMVar_hsa_circ_315738,RMVar_hsa_circ_363102 13848 RMVar_ID_13848 Human_SNP_ID_269316129 A-to-I Human chr6 + 20679044 20679044 20679044 TTCCCACTTCAGCCTCCCTAGTATCTATGACTACGGGAGTGTGTCACCACACATGGCTAGATTTA TTCCCACTTCAGCCTCCCTAGTATCTATGACTGCGGGAGTGTGTCACCACACATGGCTAGATTTA A G CDKAL1 Ensembl:ENSG00000145996 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569138540 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 13849 RMVar_ID_13849 Human_SNP_ID_269341770 A-to-I Human chr6 + 20786704 20786704 20786704 TATTTTTAGTGGAGACGAGGTTTCACCGTATTAACCAGGATGGTCTCGATCTCCTGACCTCATGA TATTTTTAGTGGAGACGAGGTTTCACCGTATTCACCAGGATGGTCTCGATCTCCTGACCTCATGA A C CDKAL1 Ensembl:ENSG00000145996 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1422815158 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_237521,RMVar_hsa_circ_2508,RMVar_hsa_circ_66259,RMVar_hsa_circ_333900,RMVar_hsa_circ_330336,RMVar_hsa_circ_36305,RMVar_hsa_circ_69831,RMVar_hsa_circ_362991,RMVar_hsa_circ_365650,RMVar_hsa_circ_359619,RMVar_hsa_circ_278802,RMVar_hsa_circ_237518,RMVar_hsa_circ_301824,RMVar_hsa_circ_336597,RMVar_hsa_circ_277499,RMVar_hsa_circ_273549,RMVar_hsa_circ_237523,RMVar_hsa_circ_237524,RMVar_hsa_circ_237522,RMVar_hsa_circ_237519,RMVar_hsa_circ_237520 13850 RMVar_ID_13850 Human_SNP_ID_269368860 A-to-I Human chr6 + 20899632 20899632 20899632 TTGGGAGCCCGAGGCAGGCAGATCACCGAGGTAAGGAGTTCGAGACCAGCCTGGCCAACATGGTG TTGGGAGCCCGAGGCAGGCAGATCACCGAGGTGAGGAGTTCGAGACCAGCCTGGCCAACATGGTG A G CDKAL1 Ensembl:ENSG00000145996 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1416911272 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2508,RMVar_hsa_circ_66259,RMVar_hsa_circ_36305,RMVar_hsa_circ_362991,RMVar_hsa_circ_359619,RMVar_hsa_circ_278802,RMVar_hsa_circ_301824,RMVar_hsa_circ_336597,RMVar_hsa_circ_277499,RMVar_hsa_circ_237519,RMVar_hsa_circ_237520,RMVar_hsa_circ_312954,RMVar_hsa_circ_376778,RMVar_hsa_circ_112975,RMVar_hsa_circ_237526,RMVar_hsa_circ_53693 13851 RMVar_ID_13851 Human_SNP_ID_269377109 A-to-I Human chr6 + 20934616 20934616 20934616 CCTATAATCCCAGCACTTTGGGAGGCTGAGACAGAAGGAACACTTGAGCCCAGGAGTTCAAGACC CCTATAATCCCAGCACTTTGGGAGGCTGAGACGGAAGGAACACTTGAGCCCAGGAGTTCAAGACC A G CDKAL1 Ensembl:ENSG00000145996 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1561896338 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2508,RMVar_hsa_circ_66259,RMVar_hsa_circ_36305,RMVar_hsa_circ_362991,RMVar_hsa_circ_359619,RMVar_hsa_circ_278802,RMVar_hsa_circ_301824,RMVar_hsa_circ_336597,RMVar_hsa_circ_277499,RMVar_hsa_circ_237519,RMVar_hsa_circ_237520,RMVar_hsa_circ_312954,RMVar_hsa_circ_376778,RMVar_hsa_circ_112975,RMVar_hsa_circ_237526,RMVar_hsa_circ_53693 13852 RMVar_ID_13852 Human_SNP_ID_269379078 A-to-I Human chr6 + 20942467 20942467 20942467 TCGGCTCACTGCAACCTTCCTCTCCTGGGTTCAAGCGATTCTCCTGCCGCAGCCTTCCAAGTAGC TCGGCTCACTGCAACCTTCCTCTCCTGGGTTCCAGCGATTCTCCTGCCGCAGCCTTCCAAGTAGC A C CDKAL1 Ensembl:ENSG00000145996 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1292785695 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2508,RMVar_hsa_circ_66259,RMVar_hsa_circ_36305,RMVar_hsa_circ_362991,RMVar_hsa_circ_359619,RMVar_hsa_circ_278802,RMVar_hsa_circ_301824,RMVar_hsa_circ_336597,RMVar_hsa_circ_277499,RMVar_hsa_circ_237519,RMVar_hsa_circ_237520,RMVar_hsa_circ_312954,RMVar_hsa_circ_376778,RMVar_hsa_circ_112975,RMVar_hsa_circ_237526,RMVar_hsa_circ_53693 13853 RMVar_ID_13853 Human_SNP_ID_269387395 A-to-I Human chr6 + 20977757 20977757 20977757 AAGATTAGCTGGACGTGGTGATGCACATGTGTAGTCCCAGCTATTCTGAAGACTGAGGCAGGAAG AAGATTAGCTGGACGTGGTGATGCACATGTGTGGTCCCAGCTATTCTGAAGACTGAGGCAGGAAG A G CDKAL1 Ensembl:ENSG00000145996 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1171883043 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2508,RMVar_hsa_circ_66259,RMVar_hsa_circ_36305,RMVar_hsa_circ_362991,RMVar_hsa_circ_359619,RMVar_hsa_circ_278802,RMVar_hsa_circ_336597,RMVar_hsa_circ_277499,RMVar_hsa_circ_237519,RMVar_hsa_circ_312954,RMVar_hsa_circ_376778,RMVar_hsa_circ_112975,RMVar_hsa_circ_303614,RMVar_hsa_circ_237526,RMVar_hsa_circ_53693,RMVar_hsa_circ_355587,RMVar_hsa_circ_365184,RMVar_hsa_circ_327899,RMVar_hsa_circ_237527 13854 RMVar_ID_13854 Human_SNP_ID_269589832 A-to-I Human chr6 + 21798700 21798700 21798700 TGCCACCACATTCATCTAATTTTCTATTTTTTATAGAGACAGAGTCTTGCTATGTTGCCCAGGCT TGCCACCACATTCATCTAATTTTCTATTTTTTGTAGAGACAGAGTCTTGCTATGTTGCCCAGGCT A G CASC15 Ensembl:ENSG00000272168 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1036598273 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_514,RMVar_hsa_circ_272260,RMVar_hsa_circ_19346,RMVar_hsa_circ_237544,RMVar_hsa_circ_237545,RMVar_hsa_circ_90979,RMVar_hsa_circ_283967,RMVar_hsa_circ_312356,RMVar_hsa_circ_329163,RMVar_hsa_circ_307020,RMVar_hsa_circ_271639,RMVar_hsa_circ_237548,RMVar_hsa_circ_237549,RMVar_hsa_circ_237550 13855 RMVar_ID_13855 Human_SNP_ID_270233238 A-to-I Human chr6 - 24278136 24278136 24278136 ACTCATCTCCTCAGCCCCTGAAGAGGAAAGGGAAAAAAGAAGACGTGAATTCAGAAAAACTGACG ACTCATCTCCTCAGCCCCTGAAGAGGAAAGGGGAAAAAGAAGACGTGAATTCAGAAAAACTGACG T C DCDC2 Ensembl:ENSG00000146038 Protein coding CDS GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_9400019,Human_RBP_ID_24548755,Human_RBP_ID_26353105 Human_Splice_Rec_743120,Human_Splice_Rec_743121 RMVar_hsa_circ_55783,RMVar_hsa_circ_73754,RMVar_hsa_circ_364954,RMVar_hsa_circ_351347,RMVar_hsa_circ_65670,RMVar_hsa_circ_299580,RMVar_hsa_circ_354099,RMVar_hsa_circ_357954,RMVar_hsa_circ_353214,RMVar_hsa_circ_65321 13856 RMVar_ID_13856 Human_SNP_ID_270266455 A-to-I Human chr6 + 24411079 24411072 24411079 AGGCATGGTGGCGGGTGCCTGTAATTCCAGCTACTCAGGAGGCTGAGGTAGGAGAATAGCTTGAA AGGCATGGTGGCGGGTGCCTGTAATT_______CTCAGGAGGCTGAGGTAGGAGAATAGCTTGAA TCCAGCTA T MRS2 Ensembl:ENSG00000124532 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1212905697 Functional Loss DEL dbSNP153 27..33 33 - - - 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_299292,RMVar_hsa_circ_335616,RMVar_hsa_circ_55878 13857 RMVar_ID_13857 Human_SNP_ID_270271423 A-to-I Human chr6 - 24428476 24428476 24428476 CTATTGCAGGAACAGAAAACCAAACACTCCATATTCTCACTTGTAAGTGGGAGCTAAATGAGAAC CTATTGCAGGAACAGAAAACCAAACACTCCATGTTCTCACTTGTAAGTGGGAGCTAAATGAGAAC T C GPLD1 Ensembl:ENSG00000112293 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1126621 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267061 13858 RMVar_ID_13858 Human_SNP_ID_270291742 A-to-I Human chr6 + 24499274 24499274 24499274 AGATGGCGCCACTGTACTCCAGCCTGGGTGACAGAGCGAGACTGTCTCAAAAAACAAAAATGAAG AGATGGCGCCACTGTACTCCAGCCTGGGTGACGGAGCGAGACTGTCTCAAAAAACAAAAATGAAG A G ALDH5A1 Ensembl:ENSG00000112294 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs539357285 Functional Loss SNV dbSNP153 33..33 33 - - - 13859 RMVar_ID_13859 Human_SNP_ID_270291823 A-to-I Human chr6 + 24499586 24499586 24499586 CTATCATTGGCTCACTGCAGCCTCAAACTCATAGGCCTAAGCGATTCCCCCACCTCAGCCTTCTG CTATCATTGGCTCACTGCAGCCTCAAACTCATGGGCCTAAGCGATTCCCCCACCTCAGCCTTCTG A G ALDH5A1 Ensembl:ENSG00000112294 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1305582264 Functional Loss SNV dbSNP153 33..33 33 - - - 13860 RMVar_ID_13860 Human_SNP_ID_270332080 A-to-I Human chr6 - 24666595 24666595 24666595 TGCCTTTGTTTTTCAGAGGGCTCTGAACTCCTACTTCGAGCCTCCGGTGGAGGAGAGCGCCTTGG TGCCTTTGTTTTTCAGAGGGCTCTGAACTCCTGCTTCGAGCCTCCGGTGGAGGAGAGCGCCTTGG T C TDP2 Ensembl:ENSG00000111802 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1253362218 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_949102,Human_RBP_ID_22460412,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 13861 RMVar_ID_13861 Human_SNP_ID_270341372 A-to-I Human chr6 + 24703013 24703013 24703013 GGCTCAAGACATTCTTCCACCTCAGTCTCCTGAGTAGCTGGAACTACAGGCGTGTGCCACCACGC GGCTCAAGACATTCTTCCACCTCAGTCTCCTGCGTAGCTGGAACTACAGGCGTGTGCCACCACGC A C ACOT13 Ensembl:ENSG00000112304 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs774612551 Functional Loss SNV dbSNP153 33..33 33 - - - 13862 RMVar_ID_13862 Human_SNP_ID_270341397 A-to-I Human chr6 + 24703062 24703062 24703062 GCGTGTGCCACCACGCCTAATTTTATTTTTGTAGAAACAAGGTCTCACTGTTGCCCAGCCTCGTC GCGTGTGCCACCACGCCTAATTTTATTTTTGTGGAAACAAGGTCTCACTGTTGCCCAGCCTCGTC A G ACOT13 Ensembl:ENSG00000112304 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215373160 Functional Loss SNV dbSNP153 33..33 33 - - - 13863 RMVar_ID_13863 Human_SNP_ID_270341689 A-to-I Human chr6 - 24704075 24704075 24704075 CTCAGGGAATGTTGATACTCTTTATCATCCATATTCGTTTTGTTGTCCCAGTATCCTTGGTAGCT CTCAGGGAATGTTGATACTCTTTATCATCCATGTTCGTTTTGTTGTCCCAGTATCCTTGGTAGCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs776408601 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7584383,Human_RBP_ID_15767119,Human_RBP_ID_17305897,Human_RBP_ID_17419137,Human_RBP_ID_18071093,Human_RBP_ID_21313615 13864 RMVar_ID_13864 Human_SNP_ID_270342008 A-to-I Human chr6 + 24705161 24705161 24705161 TTCTGCTTTTAGAACTTTGACACTCAATGGTTAATTTTACAATTTAAGATTCCAACTTTATAACC TTCTGCTTTTAGAACTTTGACACTCAATGGTTCATTTTACAATTTAAGATTCCAACTTTATAACC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1030772755 Functional Loss SNV dbSNP153 33..33 33 - - - 13865 RMVar_ID_13865 Human_SNP_ID_270342221 A-to-I Human chr6 - 24705954 24705954 24705954 TAAATCATTTTTATCTCAGAACTTAAACAAAAATTAGATGTCGTGCACGGACTGTGTGAAAGAAG TAAATCATTTTTATCTCAGAACTTAAACAAAAGTTAGATGTCGTGCACGGACTGTGTGAAAGAAG T C C6orf62 Ensembl:ENSG00000112308 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560875955 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_658803,Human_RBP_ID_1045889,Human_RBP_ID_1668558,Human_RBP_ID_2016488,Human_RBP_ID_3803863,Human_RBP_ID_7584456,Human_RBP_ID_8140966,Human_RBP_ID_8898967,Human_RBP_ID_15767234,Human_RBP_ID_17305907,Human_RBP_ID_17419148,Human_RBP_ID_17535092,Human_RBP_ID_18369395,Human_RBP_ID_18860326,Human_RBP_ID_24152662,Human_RBP_ID_24511812,Human_RBP_ID_26045546,Human_RBP_ID_27093497,Human_RBP_ID_27521746,Human_RBP_ID_27753839 Human_miRNA_ID_186296 13866 RMVar_ID_13866 Human_SNP_ID_270342224 A-to-I Human chr6 - 24705984 24705984 24705984 ATTTTGAAACTTGTTCATCCTGGATTTTTTTAAATCATTTTTATCTCAGAACTTAAACAAAAATT ATTTTGAAACTTGTTCATCCTGGATTTTTTTACATCATTTTTATCTCAGAACTTAAACAAAAATT T G C6orf62 Ensembl:ENSG00000112308 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs932112225 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_81467,Human_RBP_ID_2016488,Human_RBP_ID_7584457,Human_RBP_ID_8144473,Human_RBP_ID_15767243,Human_RBP_ID_17041744,Human_RBP_ID_17305908,Human_RBP_ID_17419149,Human_RBP_ID_17535092,Human_RBP_ID_18071109,Human_RBP_ID_18860326,Human_RBP_ID_23058925,Human_RBP_ID_23293795,Human_RBP_ID_24511813,Human_RBP_ID_27093497,Human_RBP_ID_27753841 13867 RMVar_ID_13867 Human_SNP_ID_270342423 A-to-I Human chr6 + 24706710 24706710 24706710 GAGTCAGGAGGATTGCTTGAGCCCAAGAGTTCAAGACCATTCTGGGCAACATGACGAAAACCCAT GAGTCAGGAGGATTGCTTGAGCCCAAGAGTTCGAGACCATTCTGGGCAACATGACGAAAACCCAT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1313614628 Functional Loss SNV dbSNP153 33..33 33 - - - 13868 RMVar_ID_13868 Human_SNP_ID_270342433 A-to-I Human chr6 - 24706746 24706746 24706746 CACCACATCCAGCTAATTTTTATATTTTTTGTAGAGATGGGTTTTCGTCATGTTGCCCAGAATGG CACCACATCCAGCTAATTTTTATATTTTTTGTGGAGATGGGTTTTCGTCATGTTGCCCAGAATGG T C C6orf62 Ensembl:ENSG00000112308 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs978264329 Functional Loss SNV dbSNP153 33..33 33 - - - 13869 RMVar_ID_13869 Human_SNP_ID_270342436 A-to-I Human chr6 - 24706764 24706764 24706764 TGGACTACAGGCGTGTGCCACCACATCCAGCTAATTTTTATATTTTTTGTAGAGATGGGTTTTCG TGGACTACAGGCGTGTGCCACCACATCCAGCTGATTTTTATATTTTTTGTAGAGATGGGTTTTCG T C C6orf62 Ensembl:ENSG00000112308 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs912036260 Functional Loss SNV dbSNP153 33..33 33 - - - 13870 RMVar_ID_13870 Human_SNP_ID_270342485 A-to-I Human chr6 - 24706903 24706903 24706903 ATGCTTAAATCTTTTATTTATTTTTTGAGACAAGGTCTCAACTCTGTCACCACGCTGGAGTACAC ATGCTTAAATCTTTTATTTATTTTTTGAGACAGGGTCTCAACTCTGTCACCACGCTGGAGTACAC T C C6orf62 Ensembl:ENSG00000112308 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs966965900 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15767271 13871 RMVar_ID_13871 Human_SNP_ID_270343531 A-to-I Human chr6 - 24710377 24710359 24710377 GCCTGTATTCCAGCTACTTGGGAGGCTGAGGCAGAAGAATCGCTTGAACCCAGGAGGCGGAGGTT GCCTGTATTCCAGCTACTTGGGAGGCTGAGGC__________________CAGGAGGCGGAGGTT GGGTTCAAGCGATTCTTCT G C6orf62 Ensembl:ENSG00000112308 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs540792414 Functional Loss DEL dbSNP153 33..50 33 - - - Human_RBP_ID_169489 RMVar_hsa_circ_237650,RMVar_hsa_circ_49007,RMVar_hsa_circ_324037 13872 RMVar_ID_13872 Human_SNP_ID_270343541 A-to-I Human chr6 - 24710377 24710377 24710377 GCCTGTATTCCAGCTACTTGGGAGGCTGAGGCAGAAGAATCGCTTGAACCCAGGAGGCGGAGGTT GCCTGTATTCCAGCTACTTGGGAGGCTGAGGCGGAAGAATCGCTTGAACCCAGGAGGCGGAGGTT T C C6orf62 Ensembl:ENSG00000112308 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1327118937 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_169489 RMVar_hsa_circ_237650,RMVar_hsa_circ_49007,RMVar_hsa_circ_324037 13873 RMVar_ID_13873 Human_SNP_ID_270343563 A-to-I Human chr6 - 24710462 24710460 24710463 GTCGGGAGTTTGAGACCATCCTGACCAACATAAAGAAGTCCTATCTCTACTAAAAACACAAAATT GTCGGGAGTTTGAGACCATCCTGACCAACAT___GAAGTCCTATCTCTACTAAAAACACAAAATT CTTT C C6orf62 Ensembl:ENSG00000112308 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1370634268 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_17576257 RMVar_hsa_circ_237650,RMVar_hsa_circ_49007,RMVar_hsa_circ_324037 13874 RMVar_ID_13874 Human_SNP_ID_270343679 A-to-I Human chr6 - 24710833 24710833 24710833 TGTGCACCCCATGCCCAACTAATTATTTTTGTAGAGATAGGATCTCACTGTGTTGCCCGGGCTGG TGTGCACCCCATGCCCAACTAATTATTTTTGTGGAGATAGGATCTCACTGTGTTGCCCGGGCTGG T C C6orf62 Ensembl:ENSG00000112308 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1369158832 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15767386,Human_RBP_ID_18860336 RMVar_hsa_circ_237650,RMVar_hsa_circ_49007,RMVar_hsa_circ_324037 13875 RMVar_ID_13875 Human_SNP_ID_270343700 A-to-I Human chr6 - 24710892 24710892 24710892 GAACTCCCAGGCCCAAGTGATCCTCCCACCTCAACCTCATGAGTAGCTGGGACCACAGGTGTGCA GAACTCCCAGGCCCAAGTGATCCTCCCACCTCTACCTCATGAGTAGCTGGGACCACAGGTGTGCA T A C6orf62 Ensembl:ENSG00000112308 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1392154431 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_237650,RMVar_hsa_circ_49007,RMVar_hsa_circ_324037 13876 RMVar_ID_13876 Human_SNP_ID_270343710 A-to-I Human chr6 - 24710935 24710935 24710935 CAGGCTGGAGTGCAGTGGCATAGTCATGGCTCACTGCAGCCTTGAACTCCCAGGCCCAAGTGATC CAGGCTGGAGTGCAGTGGCATAGTCATGGCTCGCTGCAGCCTTGAACTCCCAGGCCCAAGTGATC T C C6orf62 Ensembl:ENSG00000112308 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1440030004 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_237650,RMVar_hsa_circ_49007,RMVar_hsa_circ_324037 13877 RMVar_ID_13877 Human_SNP_ID_270345888 A-to-I Human chr6 - 24718604 24718604 24718604 TCTGAACAGACTACGTGCTCAGCTTAGAAAGAAAAAAGAATCTCTAGCTGACCAGTTTGACTTCA TCTGAACAGACTACGTGCTCAGCTTAGAAAGAGAAAAGAATCTCTAGCTGACCAGTTTGACTTCA T C C6orf62 Ensembl:ENSG00000112308 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1446577985 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_658833,Human_RBP_ID_2016520,Human_RBP_ID_15767638,Human_RBP_ID_19016453,Human_RBP_ID_22830236 Human_Splice_Rec_743701 13878 RMVar_ID_13878 Human_SNP_ID_270346039 A-to-I Human chr6 - 24719059 24719059 24719059 TCCGGATGGATTTTAGGGATTGGTCTGGTGTCAGCTGTGTTTTATTGCACACCTAAATCCTGATT TCCGGATGGATTTTAGGGATTGGTCTGGTGTCGGCTGTGTTTTATTGCACACCTAAATCCTGATT T C C6orf62 Ensembl:ENSG00000112308 Protein coding 5'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1032456210 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_658848,Human_RBP_ID_1045904,Human_RBP_ID_1113025,Human_RBP_ID_1216501,Human_RBP_ID_1326377,Human_RBP_ID_1668610,Human_RBP_ID_2016524,Human_RBP_ID_3803890,Human_RBP_ID_4909664,Human_RBP_ID_7584595,Human_RBP_ID_8639771,Human_RBP_ID_9192702,Human_RBP_ID_15767679,Human_RBP_ID_17419159,Human_RBP_ID_18860346,Human_RBP_ID_21221473,Human_RBP_ID_22618038,Human_RBP_ID_24152724,Human_RBP_ID_27753878 13879 RMVar_ID_13879 Human_SNP_ID_270358861 A-to-I Human chr6 - 24769625 24769625 24769625 TTTGCTTATTTAAAAAAAAAAAAAAAAAGGCCAGGCGCAGTGGCTCACGCCTGTAGTCCCGGCAC TTTGCTTATTTAAAAAAAAAAAAAAAAAGGCCGGGCGCAGTGGCTCACGCCTGTAGTCCCGGCAC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1214892175 Functional Loss SNV dbSNP153 33..33 33 - - - 13880 RMVar_ID_13880 Human_SNP_ID_270361886 A-to-I Human chr6 + 24781977 24781977 24781977 GTGGCTTGTGCCTGTATTCCCAGCTACTCAGGAGGCTGAGTCAGGAGGATCACTTGAGCCTAGGA GTGGCTTGTGCCTGTATTCCCAGCTACTCAGGGGGCTGAGTCAGGAGGATCACTTGAGCCTAGGA A G GMNN Ensembl:ENSG00000112312 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1033110381 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111992,RMVar_hsa_circ_354607,RMVar_hsa_circ_237652 13881 RMVar_ID_13881 Human_SNP_ID_270364857 A-to-I Human chr6 + 24795024 24795024 24795024 TGGTCTCCCATTTAGCCAGCTCTACATGTATTAAACTCTTTTTCTATTGCAATTCCCCTGTCTTG TGGTCTCCCATTTAGCCAGCTCTACATGTATTCAACTCTTTTTCTATTGCAATTCCCCTGTCTTG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459572817 Functional Loss SNV dbSNP153 33..33 33 - - - 13882 RMVar_ID_13882 Human_SNP_ID_270365151 A-to-I Human chr6 + 24796467 24796466 24796468 TCTTTGCCCAGACAGAGCAGATTTATCAAGACAGGGGAACTGCAATAGAGAAAGATTTTAAGACA TCTTTGCCCAGACAGAGCAGATTTATCAAGAC__GGGAACTGCAATAGAGAAAGATTTTAAGACA CAG C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1554197984 Functional Loss DEL dbSNP153 33..34 33 - - - 13883 RMVar_ID_13883 Human_SNP_ID_270374065 A-to-I Human chr6 - 24840150 24840149 24840150 GCCCAAGAGTTCAAGACCGGTATGGTCAACATAGGGAGACCCTGTCTCTGCAATAAAAGAAAAAA GCCCAAGAGTTCAAGACCGGTATGGTCAACAT_GGGAGACCCTGTCTCTGCAATAAAAGAAAAAA CT C RIPOR2 Ensembl:ENSG00000111913 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs200002070 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_8004,RMVar_hsa_circ_108272,RMVar_hsa_circ_237653,RMVar_hsa_circ_8947,RMVar_hsa_circ_314074,RMVar_hsa_circ_12901,RMVar_hsa_circ_366205 13884 RMVar_ID_13884 Human_SNP_ID_270500757 A-to-I Human chr6 + 25387023 25387023 25387023 ATGATGGCCGGTGCCTGTAATCTCAGCTACTTAGGAGCCTGAGGCGGGAGAATCGTTTGAACCTG ATGATGGCCGGTGCCTGTAATCTCAGCTACTTGGGAGCCTGAGGCGGGAGAATCGTTTGAACCTG A G CARMIL1 Ensembl:ENSG00000079691 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs890740124 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 13885 RMVar_ID_13885 Human_SNP_ID_270526955 A-to-I Human chr6 + 25500896 25500893 25500897 ATTCTCCTGCCTCAGCCTCCCAAGCAGCTGGGACTACAGGCGCCCGCCACCACGCCCGGCTATTT ATTCTCCTGCCTCAGCCTCCCAAGCAGCTG____TACAGGCGCCCGCCACCACGCCCGGCTATTT GGGAC G CARMIL1 Ensembl:ENSG00000079691 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1305544179 Functional Loss DEL dbSNP153 31..34 33 - - - RMVar_hsa_circ_7479,RMVar_hsa_circ_335092,RMVar_hsa_circ_28266,RMVar_hsa_circ_75245,RMVar_hsa_circ_11764,RMVar_hsa_circ_29101,RMVar_hsa_circ_237677,RMVar_hsa_circ_237678,RMVar_hsa_circ_237679,RMVar_hsa_circ_54282,RMVar_hsa_circ_376628,RMVar_hsa_circ_304091,RMVar_hsa_circ_316716,RMVar_hsa_circ_53498,RMVar_hsa_circ_314993,RMVar_hsa_circ_308517,RMVar_hsa_circ_237683,RMVar_hsa_circ_237681,RMVar_hsa_circ_237682,RMVar_hsa_circ_53242,RMVar_hsa_circ_24127,RMVar_hsa_circ_287875,RMVar_hsa_circ_298895,RMVar_hsa_circ_8251,RMVar_hsa_circ_55474,RMVar_hsa_circ_25650,RMVar_hsa_circ_303419,RMVar_hsa_circ_290991,RMVar_hsa_circ_282754,RMVar_hsa_circ_31797,RMVar_hsa_circ_21004,RMVar_hsa_circ_237693,RMVar_hsa_circ_237694,RMVar_hsa_circ_237691,RMVar_hsa_circ_237692,RMVar_hsa_circ_25613,RMVar_hsa_circ_116715,RMVar_hsa_circ_41997,RMVar_hsa_circ_55320,RMVar_hsa_circ_237702,RMVar_hsa_circ_55504,RMVar_hsa_circ_344699,RMVar_hsa_circ_368644,RMVar_hsa_circ_55951,RMVar_hsa_circ_53477,RMVar_hsa_circ_237703,RMVar_hsa_circ_237705,RMVar_hsa_circ_46225,RMVar_hsa_circ_237704 13886 RMVar_ID_13886 Human_SNP_ID_270526989 A-to-I Human chr6 + 25501005 25501005 25501005 AGGATGGTCTGGATCTCCTGACCTCATGATCCACCCGCCTCAGCCTCCCAAAGTGTTGGAATTAC AGGATGGTCTGGATCTCCTGACCTCATGATCCCCCCGCCTCAGCCTCCCAAAGTGTTGGAATTAC A C CARMIL1 Ensembl:ENSG00000079691 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1165269814 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7479,RMVar_hsa_circ_335092,RMVar_hsa_circ_28266,RMVar_hsa_circ_75245,RMVar_hsa_circ_11764,RMVar_hsa_circ_29101,RMVar_hsa_circ_237677,RMVar_hsa_circ_237678,RMVar_hsa_circ_237679,RMVar_hsa_circ_54282,RMVar_hsa_circ_376628,RMVar_hsa_circ_304091,RMVar_hsa_circ_316716,RMVar_hsa_circ_53498,RMVar_hsa_circ_314993,RMVar_hsa_circ_308517,RMVar_hsa_circ_237683,RMVar_hsa_circ_237681,RMVar_hsa_circ_237682,RMVar_hsa_circ_53242,RMVar_hsa_circ_24127,RMVar_hsa_circ_287875,RMVar_hsa_circ_298895,RMVar_hsa_circ_8251,RMVar_hsa_circ_55474,RMVar_hsa_circ_25650,RMVar_hsa_circ_303419,RMVar_hsa_circ_290991,RMVar_hsa_circ_282754,RMVar_hsa_circ_31797,RMVar_hsa_circ_21004,RMVar_hsa_circ_237693,RMVar_hsa_circ_237694,RMVar_hsa_circ_237691,RMVar_hsa_circ_237692,RMVar_hsa_circ_25613,RMVar_hsa_circ_116715,RMVar_hsa_circ_41997,RMVar_hsa_circ_55320,RMVar_hsa_circ_237702,RMVar_hsa_circ_55504,RMVar_hsa_circ_344699,RMVar_hsa_circ_368644,RMVar_hsa_circ_55951,RMVar_hsa_circ_53477,RMVar_hsa_circ_237703,RMVar_hsa_circ_237705,RMVar_hsa_circ_46225,RMVar_hsa_circ_237704 13887 RMVar_ID_13887 Human_SNP_ID_270544389 A-to-I Human chr6 + 25584846 25584846 25584846 GGGAAGATGAGAATGACCTTCCTGCTTTTGCTATTTCCTCAAATGCCAAGGCACCATATTTTGGG GGGAAGATGAGAATGACCTTCCTGCTTTTGCTGTTTCCTCAAATGCCAAGGCACCATATTTTGGG A G CARMIL1 Ensembl:ENSG00000079691 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1035656821 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7479,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_47078,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_48363,RMVar_hsa_circ_356312 13888 RMVar_ID_13888 Human_SNP_ID_270634169 A-to-I Human chr6 + 25978766 25978766 25978766 TCGACTCACTGCAATCTCCACCTCCCAGGCTCAAGTGATCCTCTCACCTCAGCTTCCCGAGTAGC TCGACTCACTGCAATCTCCACCTCCCAGGCTCCAGTGATCCTCTCACCTCAGCTTCCCGAGTAGC A C TRIM38 Ensembl:ENSG00000112343 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1004506414 Functional Loss SNV dbSNP153 33..33 33 - - - 13889 RMVar_ID_13889 Human_SNP_ID_270635763 A-to-I Human chr6 + 25986307 25986307 25986307 CTGTCACTTTGGGAGGCTGAGATGGGAGGATCACTTGAGGCTAGGAGTTTGAGACTAGCCTGGGC CTGTCACTTTGGGAGGCTGAGATGGGAGGATCCCTTGAGGCTAGGAGTTTGAGACTAGCCTGGGC A C TRIM38 Ensembl:ENSG00000112343 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1488181863 Functional Loss SNV dbSNP153 33..33 33 - - - 13890 RMVar_ID_13890 Human_SNP_ID_270635777 A-to-I Human chr6 + 25986409 25986409 25986409 CATGGTGGCATGTGCCTTAGTTTCAGCTACTCAGGAGGCTGAGACGAGGATTGCTTGAGCCTAGG CATGGTGGCATGTGCCTTAGTTTCAGCTACTCGGGAGGCTGAGACGAGGATTGCTTGAGCCTAGG A G TRIM38 Ensembl:ENSG00000112343 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs575301567 Functional Loss SNV dbSNP153 33..33 33 - - - 13891 RMVar_ID_13891 Human_SNP_ID_270636390 A-to-I Human chr6 + 25988594 25988594 25988594 TGGCTCACTGCAACCTCCATCTCCCAGGTTCAAACGATTCTCATATCTCAGCCTCCCGAGTAGCT TGGCTCACTGCAACCTCCATCTCCCAGGTTCAGACGATTCTCATATCTCAGCCTCCCGAGTAGCT A G TRIM38 Ensembl:ENSG00000112343 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1372378021 Functional Loss SNV dbSNP153 33..33 33 - - - 13892 RMVar_ID_13892 Human_SNP_ID_270641549 A-to-I Human chr6 + 26012989 26012989 26012989 ACCACTTTCAAAAAGAGTTTAGCATTTGACCCAACAATTCCTCTCCTAGGTATACAAACAAAATA ACCACTTTCAAAAAGAGTTTAGCATTTGACCCTACAATTCCTCTCCTAGGTATACAAACAAAATA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1561911351 Functional Loss SNV dbSNP153 33..33 33 - - - 13893 RMVar_ID_13893 Human_SNP_ID_270656882 A-to-I Human chr6 + 26056435 26056435 26056435 GGAGCGGCAGGAGCAGTCTCGGACATGTTGAGAATCAAAAACTCGGGTACAAGTGGCAAAGCGCC GGAGCGGCAGGAGCAGTCTCGGACATGTTGAGCATCAAAAACTCGGGTACAAGTGGCAAAGCGCC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs774223681 Functional Loss SNV dbSNP153 33..33 33 - - - 13894 RMVar_ID_13894 Human_SNP_ID_270666231 A-to-I Human chr6 + 26094800 26094800 26094800 TGTGATGTGAGTTGCACAGCTATGAAGGCTGTACACTGCACGAATGGAAGAGGCACCTGTCCCAG TGTGATGTGAGTTGCACAGCTATGAAGGCTGTGCACTGCACGAATGGAAGAGGCACCTGTCCCAG A G HFE Ensembl:ENSG00000010704 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1045533 Functional Loss SNV dbSNP153 33..33 33 - - - 13895 RMVar_ID_13895 Human_SNP_ID_270666340 A-to-I Human chr6 + 26095234 26095234 26095234 GAAGTAGGCCGGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAAGCGGGTGG GAAGTAGGCCGGGCACGGTGGCTCACGCCTGTTATCCCAGCACTTTGGGAGGCCAAAGCGGGTGG A T HFE Ensembl:ENSG00000010704 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1375405639 Functional Loss SNV dbSNP153 33..33 33 - - - 13896 RMVar_ID_13896 Human_SNP_ID_270666616 A-to-I Human chr6 + 26096365 26096365 26096365 CATGTTGGCCAGGCTGGTCTCGAACTCTCCTGACCTCGTGATCCGCCTGCCTCGGCCTCCCAAAG CATGTTGGCCAGGCTGGTCTCGAACTCTCCTGGCCTCGTGATCCGCCTGCCTCGGCCTCCCAAAG A G HFE Ensembl:ENSG00000010704 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs957558398 Functional Loss SNV dbSNP153 33..33 33 - - - 13897 RMVar_ID_13897 Human_SNP_ID_270676572 A-to-I Human chr6 + 26129385 26129385 26129385 TCCACTCATTGCAACCTCCTGCTCCCAGGTTCAAGCAATTCTACCTCAGCCTCCCTAGTAACTGG TCCACTCATTGCAACCTCCTGCTCCCAGGTTCGAGCAATTCTACCTCAGCCTCCCTAGTAACTGG A G H2AC6 Ensembl:ENSG00000180573 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1313370546 Functional Loss SNV dbSNP153 33..33 33 - - - 13898 RMVar_ID_13898 Human_SNP_ID_270677371 A-to-I Human chr6 + 26132676 26132676 26132676 AACCTCCACCCCCCGGGTTTAAGCGATTCTTCAGCCTCAGCCTCCCGAGTAGCTGGGACCACAGA AACCTCCACCCCCCGGGTTTAAGCGATTCTTCGGCCTCAGCCTCCCGAGTAGCTGGGACCACAGA A G H2AC6 Ensembl:ENSG00000180573 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1429902855 Functional Loss SNV dbSNP153 33..33 33 - - - 13899 RMVar_ID_13899 Human_SNP_ID_270678524 A-to-I Human chr6 + 26136889 26136889 26136889 AGGATTACAGGTGCATGCTGCCACACCTGGCTAGTTTTTGTATTTTTAGTAAAGATGGAGTTTCA AGGATTACAGGTGCATGCTGCCACACCTGGCTGGTTTTTGTATTTTTAGTAAAGATGGAGTTTCA A G H2AC6 Ensembl:ENSG00000180573 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs897200134 Functional Loss SNV dbSNP153 33..33 33 - - - 13900 RMVar_ID_13900 Human_SNP_ID_270688786 A-to-I Human chr6 + 26172297 26172297 26172297 CACGAGTTCAGGAGATAGAGACCATCCTGGCTAACACCGTGAGACCCCGTCCCTATCAAAAGTAC CACGAGTTCAGGAGATAGAGACCATCCTGGCTGACACCGTGAGACCCCGTCCCTATCAAAAGTAC A G H2BC6 Ensembl:ENSG00000274290 Protein coding 5'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs975760458 Functional Loss SNV dbSNP153 33..33 33 - - - 13901 RMVar_ID_13901 Human_SNP_ID_270688823 A-to-I Human chr6 + 26172427 26172427 26172427 AGAATCGCTAGAACCAGGGAGGCGGAGGTTGCAGTGACCGAGATCGCGCCGCTGCACTCCAGCCT AGAATCGCTAGAACCAGGGAGGCGGAGGTTGCCGTGACCGAGATCGCGCCGCTGCACTCCAGCCT A C H2BC6 Ensembl:ENSG00000274290 Protein coding 5'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs548196992 Functional Loss SNV dbSNP153 33..33 33 - - - 13902 RMVar_ID_13902 Human_SNP_ID_270689029 A-to-I Human chr6 + 26173089 26173086 26173089 GCTCTGTCCCCCAGGCTGGAGTACAGTGGCGCAGTCTCGGCTCACTGCAAGCTCTGCCTCCCGGG GCTCTGTCCCCCAGGCTGGAGTACAGTGGC___GTCTCGGCTCACTGCAAGCTCTGCCTCCCGGG CGCA C H2BC6 Ensembl:ENSG00000274290 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1193886590 Functional Loss DEL dbSNP153 31..33 33 - - - 13903 RMVar_ID_13903 Human_SNP_ID_270689385 A-to-I Human chr6 + 26174453 26174453 26174453 CCCAGCTACTCAGGAGGTGAAGCAGAAGGACCACTTGAGCCCAGGAATTGGAGACTGTAGTGTGC CCCAGCTACTCAGGAGGTGAAGCAGAAGGACCGCTTGAGCCCAGGAATTGGAGACTGTAGTGTGC A G H2BC6 Ensembl:ENSG00000274290 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs3178648 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7585812,Human_RBP_ID_15770295 13904 RMVar_ID_13904 Human_SNP_ID_270692632 A-to-I Human chr6 - 26185838 26185838 26185838 TTCTCCTATTCTTCTGCCTCAGCTTCCCAAGTAGCTGGGACTACAGGCCTGTGATACTATGCTCA TTCTCCTATTCTTCTGCCTCAGCTTCCCAAGTGGCTGGGACTACAGGCCTGTGATACTATGCTCA T C RF00017-4518 RNACentral:URS000098982A SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1258080039 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76721,RMVar_hsa_circ_237739,RMVar_hsa_circ_93634,RMVar_hsa_circ_237741 13905 RMVar_ID_13905 Human_SNP_ID_270695823 A-to-I Human chr6 - 26196100 26196100 26196100 GTGATGCCAAGAGTTCGAGACCAGCCTGCCCAACACATTGAAACTTCGTCTCTACTGAGAATACA GTGATGCCAAGAGTTCGAGACCAGCCTGCCCAGCACATTGAAACTTCGTCTCTACTGAGAATACA T C AL031777.2 Ensembl:ENSG00000282988 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1402959135 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18084719,Human_RBP_ID_27521941 RMVar_hsa_circ_76721,RMVar_hsa_circ_237739,RMVar_hsa_circ_93634,RMVar_hsa_circ_237741 13906 RMVar_ID_13906 Human_SNP_ID_270714206 A-to-I Human chr6 - 26249826 26249826 26249826 ACAAAAATACGGGTGTGGTGGCGCCCTCCTGCAGTCCCAGCTATATCGGGGGCTGAGGAAGGAGA ACAAAAATACGGGTGTGGTGGCGCCCTCCTGCGGTCCCAGCTATATCGGGGGCTGAGGAAGGAGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1307986947 Functional Loss SNV dbSNP153 33..33 33 - - - 13907 RMVar_ID_13907 Human_SNP_ID_270718893 A-to-I Human chr6 - 26266886 26266886 26266886 GTCCCAGCTGCTCTGAAGGCTGAGGCATGAGAATCGTTTGTACCTGGGAGGTGGAGGTTGCAGTG GTCCCAGCTGCTCTGAAGGCTGAGGCATGAGAGTCGTTTGTACCTGGGAGGTGGAGGTTGCAGTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1281793813 Functional Loss SNV dbSNP153 33..33 33 - - - 13908 RMVar_ID_13908 Human_SNP_ID_270722121 A-to-I Human chr6 - 26278328 26278328 26278328 GGTGCACACCACCACACCGGAGTAATTTTTGTATTTTCTGTAGAGATGGGGTTTAACCATGTTAC GGTGCACACCACCACACCGGAGTAATTTTTGTGTTTTCTGTAGAGATGGGGTTTAACCATGTTAC T C H4C8 Ensembl:ENSG00000158406 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1227868309 Functional Loss SNV dbSNP153 33..33 33 - - - 13909 RMVar_ID_13909 Human_SNP_ID_270744650 A-to-I Human chr6 + 26367988 26367988 26367988 TGTCCTGATCAGATAACAGATATTATTTTTACAGATGGTTTTCCATACTGGAACCCAAAGGTAAA TGTCCTGATCAGATAACAGATATTATTTTTACGGATGGTTTTCCATACTGGAACCCAAAGGTAAA A G BTN3A2 Ensembl:ENSG00000186470 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1287562187 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_745133,Human_Splice_Rec_745139,Human_Splice_Rec_745173,Human_Splice_Rec_745179,Human_Splice_Rec_745187,Human_Splice_Rec_745207,Human_Splice_Rec_745221,Human_Splice_Rec_745229,Human_Splice_Rec_745236,Human_Splice_Rec_745237,Human_Splice_Rec_745257,Human_Splice_Rec_745281,Human_Splice_Rec_745301 13910 RMVar_ID_13910 Human_SNP_ID_270758374 A-to-I Human chr6 + 26423926 26423926 26423926 CAAGCAATTCTCCCTGCCTCAGCCTCCTGAGTAGGTGGGATTATAGGCATGCATCACCACACCTG CAAGCAATTCTCCCTGCCTCAGCCTCCTGAGTGGGTGGGATTATAGGCATGCATCACCACACCTG A G BTN2A3P Ensembl:ENSG00000124549 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1056699334 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32320,RMVar_hsa_circ_237753,RMVar_hsa_circ_237755,RMVar_hsa_circ_237758,RMVar_hsa_circ_237757,RMVar_hsa_circ_125924,RMVar_hsa_circ_99426 13911 RMVar_ID_13911 Human_SNP_ID_270786323 A-to-I Human chr6 + 26543718 26543718 26543718 GGGAGGCAGAGGTTGCAGTGAGCCGAGATCGCACCACTGCACTCCAGCCTGGGTGACAGAACGAG GGGAGGCAGAGGTTGCAGTGAGCCGAGATCGCGCCACTGCACTCCAGCCTGGGTGACAGAACGAG A G HMGN4 Ensembl:ENSG00000182952 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1431477380 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82159,RMVar_hsa_circ_237762 13912 RMVar_ID_13912 Human_SNP_ID_270793867 A-to-I Human chr6 - 26571900 26571900 26571900 AATTAGCTCAAATGGTAGAGCGCTCGCTTAGCATGCGAGAGGTAGCGGGATCGATGCCCGCATTC AATTAGCTCAAATGGTAGAGCGCTCGCTTAGCGTGCGAGAGGTAGCGGGATCGATGCCCGCATTC T C tRNA-Ala-AGC-11-1 RNACentral:URS000052A1C9 tRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs543828299 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1046140,Human_RBP_ID_1216676,Human_RBP_ID_1669130,Human_RBP_ID_3001149,Human_RBP_ID_5450914,Human_RBP_ID_5617700,Human_RBP_ID_8640302,Human_RBP_ID_17041808,Human_RBP_ID_18071619,Human_RBP_ID_18210946,Human_RBP_ID_18860886,Human_RBP_ID_21315585,Human_RBP_ID_22830498,Human_RBP_ID_23139344,Human_RBP_ID_23293844,Human_RBP_ID_26534608 13913 RMVar_ID_13913 Human_SNP_ID_270871291 A-to-I Human chr6 - 27003848 27003848 27003848 TCCCCTCCCAGTTCAAGTGATTCACGTGCCTCAGCCTCCCGAATACCTGGGATTACAGGCATGCG TCCCCTCCCAGTTCAAGTGATTCACGTGCCTCGGCCTCCCGAATACCTGGGATTACAGGCATGCG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968688883 Functional Loss SNV dbSNP153 33..33 33 - - - 13914 RMVar_ID_13914 Human_SNP_ID_270897219 A-to-I Human chr6 - 27123330 27123330 27123330 GGGACTATAGGCGAGCACCACCACACTCCACTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCA GGGACTATAGGCGAGCACCACCACACTCCACTGATTTTTGTATTTTTAGTAGAGACAGGGTTTCA T C lnc-HIST1H2BJ-5 RNACentral:URS00008B2C9A lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs958504616 Functional Loss SNV dbSNP153 33..33 33 - - - 13915 RMVar_ID_13915 Human_SNP_ID_270897230 A-to-I Human chr6 - 27123356 27123356 27123356 AATTCTGCCTCAGCCTCCTGAGAGCTGGGACTATAGGCGAGCACCACCACACTCCACTAATTTTT AATTCTGCCTCAGCCTCCTGAGAGCTGGGACTGTAGGCGAGCACCACCACACTCCACTAATTTTT T C lnc-HIST1H2BJ-5 RNACentral:URS00008B2C9A lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs987674572 Functional Loss SNV dbSNP153 33..33 33 - - - 13916 RMVar_ID_13916 Human_SNP_ID_270897238 A-to-I Human chr6 - 27123414 27123414 27123414 GCTGGAGTGCAGTGGTGCAATCTTGACTCACCACAACCTCCGCCTCCCTGATTCAAGCAATTCTG GCTGGAGTGCAGTGGTGCAATCTTGACTCACCGCAACCTCCGCCTCCCTGATTCAAGCAATTCTG T C lnc-HIST1H2BJ-5 RNACentral:URS00008B2C9A lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1214100789 Functional Loss SNV dbSNP153 33..33 33 - - - 13917 RMVar_ID_13917 Human_SNP_ID_270897555 A-to-I Human chr6 - 27124875 27124875 27124875 AGGAAGCGGAGCTTGCACTGAGCCGAGATCACACCACTGCACTCCAGCCTGGGAGACATAGGAAG AGGAAGCGGAGCTTGCACTGAGCCGAGATCACGCCACTGCACTCCAGCCTGGGAGACATAGGAAG T C lnc-HIST1H2BJ-5 RNACentral:URS00008B2C9A lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1349309614 Functional Loss SNV dbSNP153 33..33 33 - - - 13918 RMVar_ID_13918 Human_SNP_ID_270902811 A-to-I Human chr6 - 27143130 27143130 27143130 CCAGGCTGGTCCTGAACTCCTGACTTAAGGTGATCCACCTGCCTTGGCCTCCCAAAGTGCTGGCG CCAGGCTGGTCCTGAACTCCTGACTTAAGGTGGTCCACCTGCCTTGGCCTCCCAAAGTGCTGGCG T C lnc-HIST1H2BK-1 RNACentral:URS00008B29CF lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs894044277 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78453,RMVar_hsa_circ_125936,RMVar_hsa_circ_237770,RMVar_hsa_circ_237772 13919 RMVar_ID_13919 Human_SNP_ID_270902829 A-to-I Human chr6 - 27143197 27143197 27143197 CAGGTGCCCACCACCATGCCTGGCTAGTTTTTATATTTTTAGTAGAGATGGGATTTCACCATGTT CAGGTGCCCACCACCATGCCTGGCTAGTTTTTGTATTTTTAGTAGAGATGGGATTTCACCATGTT T C lnc-HIST1H2BK-1 RNACentral:URS00008B29CF lincRNA exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1031098684 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78453,RMVar_hsa_circ_125936,RMVar_hsa_circ_237770,RMVar_hsa_circ_237772 13920 RMVar_ID_13920 Human_SNP_ID_270902862 A-to-I Human chr6 - 27143338 27143338 27143338 GGAAATTTTTTTCTTTTTTTTGAGACAGTCTTACTCTGTCGCCAAGGCTGGAGTGCAGTGGCACT GGAAATTTTTTTCTTTTTTTTGAGACAGTCTTTCTCTGTCGCCAAGGCTGGAGTGCAGTGGCACT T A lnc-HIST1H2BK-1 RNACentral:URS00008B29CF lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs373419186 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78453,RMVar_hsa_circ_125936,RMVar_hsa_circ_237770,RMVar_hsa_circ_237772 13921 RMVar_ID_13921 Human_SNP_ID_270902864 A-to-I Human chr6 - 27143344 27143344 27143344 AGGAAAGGAAATTTTTTTCTTTTTTTTGAGACAGTCTTACTCTGTCGCCAAGGCTGGAGTGCAGT AGGAAAGGAAATTTTTTTCTTTTTTTTGAGACGGTCTTACTCTGTCGCCAAGGCTGGAGTGCAGT T C lnc-HIST1H2BK-1 RNACentral:URS00008B29CF lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs894855116 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78453,RMVar_hsa_circ_125936,RMVar_hsa_circ_237770,RMVar_hsa_circ_237772 13922 RMVar_ID_13922 Human_SNP_ID_270903361 A-to-I Human chr6 - 27144945 27144945 27144945 ACTAACAGTACAAAAATTAGGGGGGGCGTGGTAGCATGTGCCCGTAGTCCCAGCTACTCGGGAGG ACTAACAGTACAAAAATTAGGGGGGGCGTGGTGGCATGTGCCCGTAGTCCCAGCTACTCGGGAGG T C lnc-HIST1H2BK-1 RNACentral:URS00008B29CF lincRNA exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs12111326 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_1115,GWAS_ID_1116 RMVar_hsa_circ_78453,RMVar_hsa_circ_125936,RMVar_hsa_circ_237770,RMVar_hsa_circ_237772 13923 RMVar_ID_13923 Human_SNP_ID_270903375 A-to-I Human chr6 - 27144959 27144958 27144959 GAAACCCCGTCTCTACTAACAGTACAAAAATTAGGGGGGGCGTGGTAGCATGTGCCCGTAGTCCC GAAACCCCGTCTCTACTAACAGTACAAAAATT_GGGGGGGCGTGGTAGCATGTGCCCGTAGTCCC CT C lnc-HIST1H2BK-1 RNACentral:URS00008B29CF lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1268937435 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_78453,RMVar_hsa_circ_125936,RMVar_hsa_circ_237770,RMVar_hsa_circ_237772 13924 RMVar_ID_13924 Human_SNP_ID_270903376 A-to-I Human chr6 - 27144959 27144959 27144959 GAAACCCCGTCTCTACTAACAGTACAAAAATTAGGGGGGGCGTGGTAGCATGTGCCCGTAGTCCC GAAACCCCGTCTCTACTAACAGTACAAAAATTGGGGGGGGCGTGGTAGCATGTGCCCGTAGTCCC T C lnc-HIST1H2BK-1 RNACentral:URS00008B29CF lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs980064017 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78453,RMVar_hsa_circ_125936,RMVar_hsa_circ_237770,RMVar_hsa_circ_237772 13925 RMVar_ID_13925 Human_SNP_ID_270903377 A-to-I Human chr6 + 27144960 27144960 27144960 GGACTACGGGCACATGCTACCACGCCCCCCCTAATTTTTGTACTGTTAGTAGAGACGGGGTTTCA GGACTACGGGCACATGCTACCACGCCCCCCCTTATTTTTGTACTGTTAGTAGAGACGGGGTTTCA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1331487303 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122237,RMVar_hsa_circ_237769 13926 RMVar_ID_13926 Human_SNP_ID_270905421 A-to-I Human chr6 + 27149668 27149668 27149668 AAGTTTTGCTCTTCTTGCCCAGGCTGGAGTGCAATGGCCTGATCTCGGCTCACTGCAACCTCCAC AAGTTTTGCTCTTCTTGCCCAGGCTGGAGTGCGATGGCCTGATCTCGGCTCACTGCAACCTCCAC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs141160550 Functional Loss SNV dbSNP153 33..33 33 - - - 13927 RMVar_ID_13927 Human_SNP_ID_270983366 A-to-I Human chr6 + 27473553 27473553 27473553 CGCGCCTGTAGCTACTCAGGAGGCAGAGGCAGAAGAATCGCTTGAACCCGGGAGGAAGAGGTTGC CGCGCCTGTAGCTACTCAGGAGGCAGAGGCAGGAGAATCGCTTGAACCCGGGAGGAAGAGGTTGC A G AL021918.5 Ensembl:ENSG00000286652 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1561845962 Functional Loss SNV dbSNP153 33..33 33 - - - 13928 RMVar_ID_13928 Human_SNP_ID_271038593 A-to-I Human chr6 + 27688222 27688220 27688223 CCGGTTAGCTCAGTTGGTTAGAGCGTGGTGCTAATAACGCCAAGGTCGCGGGTTCGATCCCCGTA CCGGTTAGCTCAGTTGGTTAGAGCGTGGTGC___TAACGCCAAGGTCGCGGGTTCGATCCCCGTA CTAA C tRNA-Ile-AAT-2-1,RF00017-4544 RNACentral:URS00006C8412,RNACentral:URS000093B8FA tRNA,SRP RNA exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1554141821 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_1669462,Human_RBP_ID_4877266,Human_RBP_ID_15772528,Human_RBP_ID_18861275,Human_RBP_ID_22830700,Human_RBP_ID_26534754 13929 RMVar_ID_13929 Human_SNP_ID_271044188 A-to-I Human chr6 + 27708728 27708728 27708728 GTTGCCCAAACTGGTCGTGAACTCCTGGGCTCAAGTGCTCTGCCTGCCTCGGCCTCCCAAAGTGT GTTGCCCAAACTGGTCGTGAACTCCTGGGCTCGAGTGCTCTGCCTGCCTCGGCCTCCCAAAGTGT A G AL009179.1 Ensembl:ENSG00000281706 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1007901106 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15772640 RMVar_hsa_circ_90688,RMVar_hsa_circ_237778 13930 RMVar_ID_13930 Human_SNP_ID_271075048 A-to-I Human chr6 - 27828842 27828842 27828842 TGGTGAGGCAATTTCTCTACTAAAAATACTCAAAAATTAGCTGGGCCTGGTGGCCTGCGTATATA TGGTGAGGCAATTTCTCTACTAAAAATACTCAGAAATTAGCTGGGCCTGGTGGCCTGCGTATATA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1481583518 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8141100,Human_RBP_ID_9193054,Human_RBP_ID_18072055,Human_RBP_ID_23293867,Human_RBP_ID_27522337 13931 RMVar_ID_13931 Human_SNP_ID_271076114 A-to-I Human chr6 + 27831538 27831536 27831539 CGCCTTTGCCGCGGCCAGACATGACGAGCAAGAGGAGTCTCACCCAACGCTTTGTGAGGACTCTG CGCCTTTGCCGCGGCCAGACATGACGAGCAA___GAGTCTCACCCAACGCTTTGTGAGGACTCTG AGAG A RF00017-4544 RNACentral:URS000093B8FA SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs766252480 Functional Loss DEL dbSNP153 32..34 33 - - - 13932 RMVar_ID_13932 Human_SNP_ID_271081615 A-to-I Human chr6 + 27853478 27853478 27853478 GGAGTCTTGCCGCGTCTCCCAGGCTGGAGTGCAGTGGCGCGATCTCGGCTCACTGCAAGCTCCGC GGAGTCTTGCCGCGTCTCCCAGGCTGGAGTGCGGTGGCGCGATCTCGGCTCACTGCAAGCTCCGC A G H2BC15 Ensembl:ENSG00000233822 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1361403671 Functional Loss SNV dbSNP153 33..33 33 - - - 13933 RMVar_ID_13933 Human_SNP_ID_271081923 A-to-I Human chr6 + 27854958 27854958 27854958 GATTTTTCTGTTGTAATTTGATGGAATTGGCCAGGCGTGGTAGCTCATGCCTGTAATCCCAGCAC GATTTTTCTGTTGTAATTTGATGGAATTGGCCGGGCGTGGTAGCTCATGCCTGTAATCCCAGCAC A G H2BC15 Ensembl:ENSG00000233822 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1047890158 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24154484 13934 RMVar_ID_13934 Human_SNP_ID_271082500 A-to-I Human chr6 + 27857175 27857175 27857175 GGTTTCCTTTTAAGAAGAGGAAATTTGGGGCCAGGCATGGTGAGTCAGGCCTGTAATCCCAATAC GGTTTCCTTTTAAGAAGAGGAAATTTGGGGCCTGGCATGGTGAGTCAGGCCTGTAATCCCAATAC A T H2BC15 Ensembl:ENSG00000233822 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs923352702 Functional Loss SNV dbSNP153 33..33 33 - - - 13935 RMVar_ID_13935 Human_SNP_ID_271097328 A-to-I Human chr6 + 27911417 27911417 27911417 TGATTAAGAAGACTCTTTGCAACCAACCTTTTAAAGGCTTCCTTTACCTCTTTGTTCCTAAGTGT TGATTAAGAAGACTCTTTGCAACCAACCTTTTGAAGGCTTCCTTTACCTCTTTGTTCCTAAGTGT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1409010500 Functional Loss SNV dbSNP153 33..33 33 - - - 13936 RMVar_ID_13936 Human_SNP_ID_271098794 A-to-I Human chr6 + 27917781 27917781 27917781 CCTTTCTCTAGGGACTGAATCCTCAACTTTCTAATGCAAAAGGAATGACAATGGGGACTAAAATA CCTTTCTCTAGGGACTGAATCCTCAACTTTCTTATGCAAAAGGAATGACAATGGGGACTAAAATA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1156357823 Functional Loss SNV dbSNP153 33..33 33 - - - 13937 RMVar_ID_13937 Human_SNP_ID_271163311 A-to-I Human chr6 + 28229937 28229937 28229937 TGGAATGCAGTGGCACGATCTCGGCTCACTGCAAGCTCCGCCTCCCGGGTTCATGCCATTCTTCT TGGAATGCAGTGGCACGATCTCGGCTCACTGCCAGCTCCGCCTCCCGGGTTCATGCCATTCTTCT A C ZSCAN9 Ensembl:ENSG00000137185 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs759041371 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25993389 RMVar_hsa_circ_237791,RMVar_hsa_circ_87696,RMVar_hsa_circ_237792 13938 RMVar_ID_13938 Human_SNP_ID_271163486 A-to-I Human chr6 + 28230503 28230503 28230503 ACAGAGGAGTCCTAAGAGGTACCTATTCTTGTATGTGAGAGACAGGACAGTTAGATATGGGAGAA ACAGAGGAGTCCTAAGAGGTACCTATTCTTGTGTGTGAGAGACAGGACAGTTAGATATGGGAGAA A G ZSCAN9 Ensembl:ENSG00000137185 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1233713 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_7588269,Human_RBP_ID_10278732,Human_RBP_ID_15775858,Human_RBP_ID_24154880 GWAS_ID_1117,GWAS_ID_1118,GWAS_ID_1119,GWAS_ID_1120,GWAS_ID_1121,GWAS_ID_1122,GWAS_ID_1123,GWAS_ID_1124 RMVar_hsa_circ_237791,RMVar_hsa_circ_87696,RMVar_hsa_circ_237792,RMVar_hsa_circ_237794 13939 RMVar_ID_13939 Human_SNP_ID_271163829 A-to-I Human chr6 + 28232145 28232145 28232145 CCTGAGGTCAGGAGTTCAAGACCAGGATGGCCAACATGGCGAAACCGCGTCTGTACTAAAAATAC CCTGAGGTCAGGAGTTCAAGACCAGGATGGCCGACATGGCGAAACCGCGTCTGTACTAAAAATAC A G ZSCAN9 Ensembl:ENSG00000137185 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T4 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs761662832 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_237791,RMVar_hsa_circ_87696,RMVar_hsa_circ_237792,RMVar_hsa_circ_237794 13940 RMVar_ID_13940 Human_SNP_ID_271163844 A-to-I Human chr6 + 28232178 28232178 28232178 ACATGGCGAAACCGCGTCTGTACTAAAAATACAAAATTAGTTGGGCGTGGGGGTGCGTGCCTGTA ACATGGCGAAACCGCGTCTGTACTAAAAATACGAAATTAGTTGGGCGTGGGGGTGCGTGCCTGTA A G ZSCAN9 Ensembl:ENSG00000137185 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs766431648 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_237791,RMVar_hsa_circ_87696,RMVar_hsa_circ_237792,RMVar_hsa_circ_237794 13941 RMVar_ID_13941 Human_SNP_ID_271164233 A-to-I Human chr6 + 28233360 28233360 28233360 GGTGTTTGAAGCTACTGTTTTCTCTTTTGTTCATTTTACCTCTTTCTTACTCTTACTAGCTGTGT GGTGTTTGAAGCTACTGTTTTCTCTTTTGTTCGTTTTACCTCTTTCTTACTCTTACTAGCTGTGT A G ZSCAN9 Ensembl:ENSG00000137185 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7206 Functional Loss SNV dbSNP153,JSNP 33..33 33 - - - Human_RBP_ID_2017304,Human_RBP_ID_3805044,Human_RBP_ID_7588288,Human_RBP_ID_18072332,Human_RBP_ID_18861510,Human_RBP_ID_21901955,Human_RBP_ID_22424069 GWAS_ID_1125,GWAS_ID_1126,GWAS_ID_1127,GWAS_ID_1128,GWAS_ID_1129,GWAS_ID_1130,GWAS_ID_1131,GWAS_ID_1132 RMVar_hsa_circ_237791,RMVar_hsa_circ_87696,RMVar_hsa_circ_237792,RMVar_hsa_circ_237794,RMVar_hsa_circ_237795 13942 RMVar_ID_13942 Human_SNP_ID_271164234 A-to-I Human chr6 + 28233360 28233360 28233360 GGTGTTTGAAGCTACTGTTTTCTCTTTTGTTCATTTTACCTCTTTCTTACTCTTACTAGCTGTGT GGTGTTTGAAGCTACTGTTTTCTCTTTTGTTCTTTTTACCTCTTTCTTACTCTTACTAGCTGTGT A T ZSCAN9 Ensembl:ENSG00000137185 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7206 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2017304,Human_RBP_ID_3805044,Human_RBP_ID_7588288,Human_RBP_ID_18072332,Human_RBP_ID_18861510,Human_RBP_ID_21901955,Human_RBP_ID_22424069 GWAS_ID_1125,GWAS_ID_1126,GWAS_ID_1127,GWAS_ID_1128,GWAS_ID_1129,GWAS_ID_1130,GWAS_ID_1131,GWAS_ID_1132 RMVar_hsa_circ_237791,RMVar_hsa_circ_87696,RMVar_hsa_circ_237792,RMVar_hsa_circ_237794,RMVar_hsa_circ_237795 13943 RMVar_ID_13943 Human_SNP_ID_271172297 A-to-I Human chr6 + 28271413 28271413 28271413 TCTTTTTCTCTCTTTTCTTCCTTTTTTGATATAGGTCTTGCTCTGGTTGCCCAGGCTGAACTCAG TCTTTTTCTCTCTTTTCTTCCTTTTTTGATATTGGTCTTGCTCTGGTTGCCCAGGCTGAACTCAG A T ZSCAN26,AL021997.3 Ensembl:ENSG00000197062,Ensembl:ENSG00000276302 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1408712356 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21318142 13944 RMVar_ID_13944 Human_SNP_ID_271172329 A-to-I Human chr6 + 28271538 28271538 28271538 GTGCCACCATGCCTGGTGTCACTATGTTGCCCAGGCTGGACTCAAACTCCTGGGCTTAAGCAGTC GTGCCACCATGCCTGGTGTCACTATGTTGCCCGGGCTGGACTCAAACTCCTGGGCTTAAGCAGTC A G ZSCAN26,AL021997.3 Ensembl:ENSG00000197062,Ensembl:ENSG00000276302 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1246824988 Functional Loss SNV dbSNP153 33..33 33 - - - 13945 RMVar_ID_13945 Human_SNP_ID_271172791 A-to-I Human chr6 + 28273340 28273340 28273340 CAAGGTGGGTAGGTATACGAGGTCAGGAGTTCAAGACCAGCCTGGCCAAGATGGTGAAACACTGT CAAGGTGGGTAGGTATACGAGGTCAGGAGTTCGAGACCAGCCTGGCCAAGATGGTGAAACACTGT A G ZSCAN26,AL021997.3 Ensembl:ENSG00000197062,Ensembl:ENSG00000276302 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1007878490 Functional Loss SNV dbSNP153 33..33 33 - - - 13946 RMVar_ID_13946 Human_SNP_ID_271179237 A-to-I Human chr6 + 28302616 28302616 28302616 CACAGTCTCGCTCTGCGGCCAAGCTGGAGTGCAGTGGCACGATCTTGGCTCACTGCAACCTCTGA CACAGTCTCGCTCTGCGGCCAAGCTGGAGTGCGGTGGCACGATCTTGGCTCACTGCAACCTCTGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1360393371 Functional Loss SNV dbSNP153 33..33 33 - - - 13947 RMVar_ID_13947 Human_SNP_ID_271179243 A-to-I Human chr6 + 28302660 28302660 28302660 TTGGCTCACTGCAACCTCTGACACCCTAGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGC TTGGCTCACTGCAACCTCTGACACCCTAGTTCCAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1363842599 Functional Loss SNV dbSNP153 33..33 33 - - - 13948 RMVar_ID_13948 Human_SNP_ID_271190473 A-to-I Human chr6 + 28358763 28358763 28358763 AAAATTAGCTGGGCATGGTGGTGCACACCTATAATCCCAGCTTCTTGGGAGGCTGAGGCAGAAGA AAAATTAGCTGGGCATGGTGGTGCACACCTATGATCCCAGCTTCTTGGGAGGCTGAGGCAGAAGA A G ZKSCAN3 Ensembl:ENSG00000189298 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1347690348 Functional Loss SNV dbSNP153 33..33 33 - - - 13949 RMVar_ID_13949 Human_SNP_ID_271281450 A-to-I 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 GSE100210 HepG2 cell line - 29129909 RNA-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 13950 RMVar_ID_13950 Human_SNP_ID_271326106 A-to-I Human chr6 - 28904991 28904991 28904991 GGAGAATCACCTGAGCCCAGGAGTTTGGGGTTACAATGAACTATGACCACACCACTGCGCTCCAG GGAGAATCACCTGAGCCCAGGAGTTTGGGGTTGCAATGAACTATGACCACACCACTGCGCTCCAG T C TRIM27 Ensembl:ENSG00000204713 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1315837033 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15778139 13951 RMVar_ID_13951 Human_SNP_ID_271327513 A-to-I Human chr6 - 28910609 28910609 28910609 AAGAAATGTGCAGGTTGGGTGCGGTGGCTCACACCTGTAATCCCAGCATTTTGGGAGGCCAAGTC AAGAAATGTGCAGGTTGGGTGCGGTGGCTCACGCCTGTAATCCCAGCATTTTGGGAGGCCAAGTC T C TRIM27 Ensembl:ENSG00000204713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1258125022 Functional Loss SNV dbSNP153 33..33 33 - - - 13952 RMVar_ID_13952 Human_SNP_ID_271328161 A-to-I Human chr6 - 28913099 28913099 28913099 AGGCATACGCCACCATGCCCGGCTAATTTTGTATTTTTAGTAGAGACGGGGTTTCTCCATGTTGG AGGCATACGCCACCATGCCCGGCTAATTTTGTGTTTTTAGTAGAGACGGGGTTTCTCCATGTTGG T C TRIM27 Ensembl:ENSG00000204713 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1296267019 Functional Loss SNV dbSNP153 33..33 33 - - - 13953 RMVar_ID_13953 Human_SNP_ID_271328582 A-to-I Human chr6 - 28914295 28914295 28914295 CCCCGTCGCTATTAAAAATACAAAAATTAGCCAGGTGTGGTGGCACATGCCTGTAATCTCAGCTA CCCCGTCGCTATTAAAAATACAAAAATTAGCCGGGTGTGGTGGCACATGCCTGTAATCTCAGCTA T C TRIM27 Ensembl:ENSG00000204713 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs892821145 Functional Loss SNV dbSNP153 33..33 33 - - - 13954 RMVar_ID_13954 Human_SNP_ID_271328599 A-to-I Human chr6 - 28914362 28914362 28914362 GGGAGGCCGAGGCAGGTGGATCACATTAGGTCAGGAGTTTGAGACCAGCCTGGCCAACATGGCAA GGGAGGCCGAGGCAGGTGGATCACATTAGGTCCGGAGTTTGAGACCAGCCTGGCCAACATGGCAA T G TRIM27 Ensembl:ENSG00000204713 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1348141038 Functional Loss SNV dbSNP153 33..33 33 - - - 13955 RMVar_ID_13955 Human_SNP_ID_271328606 A-to-I Human chr6 - 28914414 28914412 28914414 TTTTATGGGATAGGCCGGGTGCAGTGACTCACACCTGTAATCCCAGTACTTTGGGAGGCCGAGGC TTTTATGGGATAGGCCGGGTGCAGTGACTCAC__CTGTAATCCCAGTACTTTGGGAGGCCGAGGC GGT G TRIM27 Ensembl:ENSG00000204713 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs545939036 Functional Loss DEL dbSNP153 33..34 33 - - - 13956 RMVar_ID_13956 Human_SNP_ID_271328608 A-to-I Human chr6 - 28914414 28914414 28914414 TTTTATGGGATAGGCCGGGTGCAGTGACTCACACCTGTAATCCCAGTACTTTGGGAGGCCGAGGC TTTTATGGGATAGGCCGGGTGCAGTGACTCACGCCTGTAATCCCAGTACTTTGGGAGGCCGAGGC T C TRIM27 Ensembl:ENSG00000204713 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1356763499 Functional Loss SNV dbSNP153 33..33 33 - - - 13957 RMVar_ID_13957 Human_SNP_ID_271328631 A-to-I Human chr6 - 28914501 28914497 28914501 AGACAAATTGACAGTCAACTTCAGATAGAAAAATAAGCACATAATAATATGCACATATAAAATAA AGACAAATTGACAGTCAACTTCAGATAGAAAA____GCACATAATAATATGCACATATAAAATAA CTTAT C TRIM27 Ensembl:ENSG00000204713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1205735300 Functional Loss DEL dbSNP153 33..36 33 - - - 13958 RMVar_ID_13958 Human_SNP_ID_271328943 A-to-I Human chr6 - 28915497 28915497 28915497 CTGAGTGAGTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCACACACCACCACACCTA CTGAGTGAGTCTCCTGCCTCAGCCTCCCGAGTTGCTGGGATTACAGGCACACACCACCACACCTA T A TRIM27 Ensembl:ENSG00000204713 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs533689327 Functional Loss SNV dbSNP153 33..33 33 - - - 13959 RMVar_ID_13959 Human_SNP_ID_271328956 A-to-I Human chr6 - 28915559 28915559 28915559 TCACTCTGTTGCCCAGGCTGGAGTGCAGTGGCACAATCTCAGCTCACTGCAGCTTCCACCTCCTG TCACTCTGTTGCCCAGGCTGGAGTGCAGTGGCGCAATCTCAGCTCACTGCAGCTTCCACCTCCTG T C TRIM27 Ensembl:ENSG00000204713 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1476276877 Functional Loss SNV dbSNP153 33..33 33 - - - 13960 RMVar_ID_13960 Human_SNP_ID_271329455 A-to-I Human chr6 - 28917540 28917540 28917540 ATACTCTTGCTCTGTTGCCCAGGCTGGAGTGCAGTGGTGCAATCTTGGCTCACTGCAACATCCCC ATACTCTTGCTCTGTTGCCCAGGCTGGAGTGCGGTGGTGCAATCTTGGCTCACTGCAACATCCCC T C TRIM27 Ensembl:ENSG00000204713 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1391004471 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15922101 13961 RMVar_ID_13961 Human_SNP_ID_271329584 A-to-I Human chr6 - 28917951 28917951 28917951 GTGGTGGCACATGCTTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACCAG GTGGTGGCACATGCTTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCAG T C TRIM27 Ensembl:ENSG00000204713 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1319479199 Functional Loss SNV dbSNP153 33..33 33 - - - 13962 RMVar_ID_13962 Human_SNP_ID_271329758 A-to-I Human chr6 - 28918618 28918618 28918618 CCTCCTCGGCCTCCCAAAGTGTTGGGATTACAAGTGTGAGCCACAGCGTCAGGCCAGTTTACATT CCTCCTCGGCCTCCCAAAGTGTTGGGATTACAGGTGTGAGCCACAGCGTCAGGCCAGTTTACATT T C TRIM27 Ensembl:ENSG00000204713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1204273559 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7589418,Human_RBP_ID_15778572 13963 RMVar_ID_13963 Human_SNP_ID_271329783 A-to-I Human chr6 - 28918710 28918710 28918710 CACCATGGCTGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATATTGGTCAGGCTGG CACCATGGCTGGCTAATTTTTGTATTTTTAGTGGAGACGGGGTTTCACCATATTGGTCAGGCTGG T C TRIM27 Ensembl:ENSG00000204713 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs182380396 Functional Loss SNV dbSNP153 33..33 33 - - - 13964 RMVar_ID_13964 Human_SNP_ID_271329898 A-to-I Human chr6 - 28919081 28919081 28919081 CAAAACCAGGAGGAAGTGGTTGCAGTGAGCCAAGATCGCGCCACTGTACTCCAGCCTGGGCAACA CAAAACCAGGAGGAAGTGGTTGCAGTGAGCCAGGATCGCGCCACTGTACTCCAGCCTGGGCAACA T C TRIM27 Ensembl:ENSG00000204713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1321167485 Functional Loss SNV dbSNP153 33..33 33 - - - 13965 RMVar_ID_13965 Human_SNP_ID_271329900 A-to-I Human chr6 - 28919099 28919099 28919099 CTGAGGCAAGGAATTGCCCAAAACCAGGAGGAAGTGGTTGCAGTGAGCCAAGATCGCGCCACTGT CTGAGGCAAGGAATTGCCCAAAACCAGGAGGATGTGGTTGCAGTGAGCCAAGATCGCGCCACTGT T A TRIM27 Ensembl:ENSG00000204713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1282669069 Functional Loss SNV dbSNP153 33..33 33 - - - 13966 RMVar_ID_13966 Human_SNP_ID_271329901 A-to-I Human chr6 - 28919099 28919099 28919099 CTGAGGCAAGGAATTGCCCAAAACCAGGAGGAAGTGGTTGCAGTGAGCCAAGATCGCGCCACTGT CTGAGGCAAGGAATTGCCCAAAACCAGGAGGAGGTGGTTGCAGTGAGCCAAGATCGCGCCACTGT T C TRIM27 Ensembl:ENSG00000204713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1282669069 Functional Loss SNV dbSNP153 33..33 33 - - - 13967 RMVar_ID_13967 Human_SNP_ID_271540423 A-to-I Human chr6 - 29829459 29829459 29829459 GCCCAGGGCCCAGCACCTCAGGGTGGCCTCATAGTCAAAGACAGGGTGGTGGGTCACGTGTGTCT GCCCAGGGCCCAGCACCTCAGGGTGGCCTCATGGTCAAAGACAGGGTGGTGGGTCACGTGTGTCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285867439 Functional Loss SNV dbSNP153 33..33 33 - - - 13968 RMVar_ID_13968 Human_SNP_ID_271574637 A-to-I Human chr6 - 29943286 29943285 29943286 GCCCGTCCGACCCCACGTCGCAGCCATACATTATCTGGATGGTGTGAGAACCTGGCCCCGACCCC GCCCGTCCGACCCCACGTCGCAGCCATACATT_TCTGGATGGTGTGAGAACCTGGCCCCGACCCC AT A HCG4B,HCG4B:2 RNACentral:URS00009B51D2,RNACentral:URS00008B26E4 lincRNA,lincRNA intron,exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs199474484 Functional Loss DEL dbSNP153 33..33 33 - - - 13969 RMVar_ID_13969 Human_SNP_ID_271574641 A-to-I Human chr6 - 29943286 29943286 29943287 GCCCGTCCGACCCCACGTCGCAGCCATACATTATCTGGATGGTGTGAGAACCTGGCCCCGACCCC GCCCGTCCGACCCCACGTCGCAGCCATACATCCTCTGGATGGTGTGAGAACCTGGCCCCGACCCC TA GG HCG4B,HCG4B:2 RNACentral:URS00009B51D2,RNACentral:URS00008B26E4 lincRNA,lincRNA intron,exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs386698553 Functional Loss MNV dbSNP153 32..33 33 - - - 13970 RMVar_ID_13970 Human_SNP_ID_271574643 A-to-I Human chr6 - 29943286 29943286 29943286 GCCCGTCCGACCCCACGTCGCAGCCATACATTATCTGGATGGTGTGAGAACCTGGCCCCGACCCC GCCCGTCCGACCCCACGTCGCAGCCATACATTTTCTGGATGGTGTGAGAACCTGGCCCCGACCCC T A HCG4B,HCG4B:2 RNACentral:URS00009B51D2,RNACentral:URS00008B26E4 lincRNA,lincRNA intron,exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs199474485 Functional Loss SNV dbSNP153 33..33 33 - - - 13971 RMVar_ID_13971 Human_SNP_ID_271574644 A-to-I Human chr6 - 29943286 29943286 29943286 GCCCGTCCGACCCCACGTCGCAGCCATACATTATCTGGATGGTGTGAGAACCTGGCCCCGACCCC GCCCGTCCGACCCCACGTCGCAGCCATACATTCTCTGGATGGTGTGAGAACCTGGCCCCGACCCC T G HCG4B,HCG4B:2 RNACentral:URS00009B51D2,RNACentral:URS00008B26E4 lincRNA,lincRNA intron,exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs199474485 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 13972 RMVar_ID_13972 Human_SNP_ID_271575404 A-to-I Human chr6 + 29944135 29944135 29944135 TTCTGACTCTTCCCGTCAGACCCCCCCAAGACACATATGACCCACCACCCCATCTCTGACCATGA TTCTGACTCTTCCCGTCAGACCCCCCCAAGACGCATATGACCCACCACCCCATCTCTGACCATGA A G HLA-A Ensembl:ENSG00000206503 Protein coding CDS GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1136749 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_Splice_Rec_747844,Human_Splice_Rec_747858,Human_Splice_Rec_747872,Human_Splice_Rec_747886,Human_Splice_Rec_747898,Human_Splice_Rec_747904,Human_Splice_Rec_747918,Human_Splice_Rec_747926,Human_Splice_Rec_747936 13973 RMVar_ID_13973 Human_SNP_ID_271575407 A-to-I Human chr6 + 29944139 29944139 29944139 GACTCTTCCCGTCAGACCCCCCCAAGACACATATGACCCACCACCCCATCTCTGACCATGAGGCC GACTCTTCCCGTCAGACCCCCCCAAGACACATGTGACCCACCACCCCATCTCTGACCATGAGGCC A G HLA-A Ensembl:ENSG00000206503 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1425587881 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_747844,Human_Splice_Rec_747858,Human_Splice_Rec_747872,Human_Splice_Rec_747886,Human_Splice_Rec_747898,Human_Splice_Rec_747904,Human_Splice_Rec_747918,Human_Splice_Rec_747926,Human_Splice_Rec_747936 13974 RMVar_ID_13974 Human_SNP_ID_410131867 A-to-I Human chr9 - 105215493 105215493 105215493 TCAGCTCACTGCAGCCTCTGCCTCCTGGGTTCAGGTGATTCTCCTGCCTCAGCCTCCTGAGTAGC TCAGCTCACTGCAGCCTCTGCCTCCTGGGTTCGGGTGATTCTCCTGCCTCAGCCTCCTGAGTAGC T C AL591506.1 Ensembl:ENSG00000286536 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1014353338 Functional Loss SNV dbSNP153 33..33 33 - - - 13975 RMVar_ID_13975 Human_SNP_ID_410131868 A-to-I Human chr9 - 105215493 105215493 105215493 TCAGCTCACTGCAGCCTCTGCCTCCTGGGTTCAGGTGATTCTCCTGCCTCAGCCTCCTGAGTAGC TCAGCTCACTGCAGCCTCTGCCTCCTGGGTTCCGGTGATTCTCCTGCCTCAGCCTCCTGAGTAGC T G AL591506.1 Ensembl:ENSG00000286536 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1014353338 Functional Loss SNV dbSNP153 33..33 33 - - - 13976 RMVar_ID_13976 Human_SNP_ID_410171186 A-to-I Human chr9 - 105383214 105383214 105383214 AGCAATGAGCGACTAGGAAAGCAAAGAGGCAGACGATGATCAGAGGCAGCACCCATACTGTGTAG AGCAATGAGCGACTAGGAAAGCAAAGAGGCAGGCGATGATCAGAGGCAGCACCCATACTGTGTAG T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs752462919 Functional Loss SNV dbSNP153 33..33 33 - - - 13977 RMVar_ID_13977 Human_SNP_ID_410214341 A-to-I Human chr9 + 105558527 105558527 105558527 ACCTCAGGTTATCCGCCCGCGTTGGCCTCTCAAAGTGCTGAGATTACAGCCGTGAGCCACCGCGC ACCTCAGGTTATCCGCCCGCGTTGGCCTCTCAGAGTGCTGAGATTACAGCCGTGAGCCACCGCGC A G FKTN Ensembl:ENSG00000106692 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs371306514 Functional Loss SNV dbSNP153 33..33 33 - - - 13978 RMVar_ID_13978 Human_SNP_ID_410506838 A-to-I Human chr9 + 106722495 106722495 106722495 TGCAGATCACTGTGTCCACTACTATGATCTTCATAACACTAAACAGCCAATCACGGTATTCAAAA TGCAGATCACTGTGTCCACTACTATGATCTTCGTAACACTAAACAGCCAATCACGGTATTCAAAA A G AL512649.1,LINC01505 Ensembl:ENSG00000228143,Ensembl:ENSG00000234323 Pseudogene,lincRNA exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1022007564 Functional Loss SNV dbSNP153 33..33 33 - - - 13979 RMVar_ID_13979 Human_SNP_ID_410614274 A-to-I Human chr9 + 107170471 107170471 107170471 GCAAAGATTTGAAAGTGTCCAGGTAAGATTACATAAGTAACCACATGCTAAAGATGACATATCAG GCAAAGATTTGAAAGTGTCCAGGTAAGATTACGTAAGTAACCACATGCTAAAGATGACATATCAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs570432153 Functional Loss SNV dbSNP153 33..33 33 - - - 13980 RMVar_ID_13980 Human_SNP_ID_410643333 A-to-I Human chr9 + 107288585 107288585 107288585 CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTAGAGGTGTGCCCCACCACACCTGGTTAATTTTT CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTGGAGGTGTGCCCCACCACACCTGGTTAATTTTT A G RAD23B Ensembl:ENSG00000119318 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs745429400 Functional Loss SNV dbSNP153 33..33 33 - - - 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_258471 13981 RMVar_ID_13981 Human_SNP_ID_410644698 A-to-I Human chr9 + 107293853 107293853 107293853 TTGCTCAGGCTGGAGTACGCTGACAAGATTATAGCTCACTCCAACCTTGAACTCCTGGGCTCAGT TTGCTCAGGCTGGAGTACGCTGACAAGATTATGGCTCACTCCAACCTTGAACTCCTGGGCTCAGT A G RAD23B Ensembl:ENSG00000119318 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1447326958 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16532554 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_258471 13982 RMVar_ID_13982 Human_SNP_ID_410653383 A-to-I Human chr9 + 107325203 107325203 107325203 TGGCGTGGTGGCACATACCTGTAATCTCAGCTACTTGGGAGGCTGAGGCAGGAGAATTGCTTGGA TGGCGTGGTGGCACATACCTGTAATCTCAGCTGCTTGGGAGGCTGAGGCAGGAGAATTGCTTGGA A G RAD23B Ensembl:ENSG00000119318 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1283525279 Functional Loss SNV dbSNP153 33..33 33 - - - 13983 RMVar_ID_13983 Human_SNP_ID_410653881 A-to-I Human chr9 + 107326779 107326779 107326779 CCTCAGCCTCCCGAGTAGCTGGGACCACAGGCACCCGCCACCATGCCCGGCTAATTTTGTTTTGT CCTCAGCCTCCCGAGTAGCTGGGACCACAGGCCCCCGCCACCATGCCCGGCTAATTTTGTTTTGT A C RAD23B Ensembl:ENSG00000119318 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1016540029 Functional Loss SNV dbSNP153 33..33 33 - - - 13984 RMVar_ID_13984 Human_SNP_ID_410657506 A-to-I Human chr9 + 107340259 107340258 107340259 CCGAGATCGTGCCACTCTACTCCACCCCGGGCAACAGAGCGAGACTCTATCTCAAAAAAACAAAA CCGAGATCGTGCCACTCTACTCCACCCCGGGC_ACAGAGCGAGACTCTATCTCAAAAAAACAAAA CA C lnc-RAD23B-2 RNACentral:URS00008B3E28 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1195989105 Functional Loss DEL dbSNP153 33..33 33 - - - 13985 RMVar_ID_13985 Human_SNP_ID_410788169 A-to-I Human chr9 + 107854157 107854157 107854157 TTGCCTTTTTCTGCTTCTGCTGAATGGTCTCCAAGTCCCTCTGCTTGCAGGAGGCAACAGAAAGC TTGCCTTTTTCTGCTTCTGCTGAATGGTCTCCTAGTCCCTCTGCTTGCAGGAGGCAACAGAAAGC A T RF00017-4490 RNACentral:URS0000922AF7 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1164407219 Functional Loss SNV dbSNP153 33..33 33 - - - 13986 RMVar_ID_13986 Human_SNP_ID_411061838 A-to-I Human chr9 - 108876266 108876266 108876266 TTTTGAAGATAATTGTTTTTGTTTTTTGAGACAGGGTCTCACTCTGTTGCTCAGGCTGGAGTGCA TTTTGAAGATAATTGTTTTTGTTTTTTGAGACGGGGTCTCACTCTGTTGCTCAGGCTGGAGTGCA T C ELP1 Ensembl:ENSG00000070061 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1429865049 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16755405 RMVar_hsa_circ_64075,RMVar_hsa_circ_258486,RMVar_hsa_circ_98912,RMVar_hsa_circ_93681,RMVar_hsa_circ_286975,RMVar_hsa_circ_90120,RMVar_hsa_circ_44376,RMVar_hsa_circ_60254,RMVar_hsa_circ_258487,RMVar_hsa_circ_258488,RMVar_hsa_circ_258489 13987 RMVar_ID_13987 Human_SNP_ID_411100091 A-to-I Human chr9 - 109033451 109033451 109033451 GACAGGCTTGGCAGTGGCCGGTGGAGCATACTACCTAGGCCTGGAAGGAGCAATCATCGGTCCTA GACAGGCTTGGCAGTGGCCGGTGGAGCATACTGCCTAGGCCTGGAAGGAGCAATCATCGGTCCTA T C TMEM245 Ensembl:ENSG00000106771 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs777132080 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8924362,Human_RBP_ID_9231487,Human_RBP_ID_17323460,Human_RBP_ID_17550744,Human_RBP_ID_22776892 Human_Splice_Rec_1070168,Human_Splice_Rec_1070174,Human_Splice_Rec_1070196,Human_Splice_Rec_1070226 Human_miRNA_ID_493014,Human_miRNA_ID_496279,Human_miRNA_ID_2168261,Human_miRNA_ID_2169784 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 13988 RMVar_ID_13988 Human_SNP_ID_411102542 A-to-I Human chr9 - 109043084 109043084 109043084 TCCAAAGAACCCTAGAGACGAGTGATAATTATATGCTCAGTATTATAGGTTATTTAAAGTAACCG TCCAAAGAACCCTAGAGACGAGTGATAATTATGTGCTCAGTATTATAGGTTATTTAAAGTAACCG T C TMEM245 Ensembl:ENSG00000106771 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1329635341 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26606,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_331093,RMVar_hsa_circ_284338,RMVar_hsa_circ_289969,RMVar_hsa_circ_279315,RMVar_hsa_circ_270820,RMVar_hsa_circ_275877,RMVar_hsa_circ_272882,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_28902,RMVar_hsa_circ_310854,RMVar_hsa_circ_328887,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_123377,RMVar_hsa_circ_106629,RMVar_hsa_circ_108676,RMVar_hsa_circ_87258,RMVar_hsa_circ_258530,RMVar_hsa_circ_258532,RMVar_hsa_circ_258533,RMVar_hsa_circ_258534,RMVar_hsa_circ_258531 13989 RMVar_ID_13989 Human_SNP_ID_411102546 A-to-I Human chr9 - 109043108 109043108 109043108 CCTAGCAATCTCTGAATTTTAGGTTCCAAAGAACCCTAGAGACGAGTGATAATTATATGCTCAGT CCTAGCAATCTCTGAATTTTAGGTTCCAAAGAGCCCTAGAGACGAGTGATAATTATATGCTCAGT T C TMEM245 Ensembl:ENSG00000106771 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1008180819 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26606,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_331093,RMVar_hsa_circ_284338,RMVar_hsa_circ_289969,RMVar_hsa_circ_279315,RMVar_hsa_circ_270820,RMVar_hsa_circ_275877,RMVar_hsa_circ_272882,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_28902,RMVar_hsa_circ_310854,RMVar_hsa_circ_328887,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_123377,RMVar_hsa_circ_106629,RMVar_hsa_circ_108676,RMVar_hsa_circ_87258,RMVar_hsa_circ_258530,RMVar_hsa_circ_258532,RMVar_hsa_circ_258533,RMVar_hsa_circ_258534,RMVar_hsa_circ_258531 13990 RMVar_ID_13990 Human_SNP_ID_411102551 A-to-I Human chr9 - 109043125 109043125 109043125 TTTGGGAGTAAATTATTCCTAGCAATCTCTGAATTTTAGGTTCCAAAGAACCCTAGAGACGAGTG TTTGGGAGTAAATTATTCCTAGCAATCTCTGATTTTTAGGTTCCAAAGAACCCTAGAGACGAGTG T A TMEM245 Ensembl:ENSG00000106771 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1320499383 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26606,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_331093,RMVar_hsa_circ_284338,RMVar_hsa_circ_289969,RMVar_hsa_circ_279315,RMVar_hsa_circ_270820,RMVar_hsa_circ_275877,RMVar_hsa_circ_272882,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_28902,RMVar_hsa_circ_310854,RMVar_hsa_circ_328887,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_123377,RMVar_hsa_circ_106629,RMVar_hsa_circ_108676,RMVar_hsa_circ_87258,RMVar_hsa_circ_258530,RMVar_hsa_circ_258532,RMVar_hsa_circ_258533,RMVar_hsa_circ_258534,RMVar_hsa_circ_258531 13991 RMVar_ID_13991 Human_SNP_ID_411102552 A-to-I Human chr9 - 109043133 109043133 109043133 TATTTGACTTTGGGAGTAAATTATTCCTAGCAATCTCTGAATTTTAGGTTCCAAAGAACCCTAGA TATTTGACTTTGGGAGTAAATTATTCCTAGCAGTCTCTGAATTTTAGGTTCCAAAGAACCCTAGA T C TMEM245 Ensembl:ENSG00000106771 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs532913335 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26606,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_331093,RMVar_hsa_circ_284338,RMVar_hsa_circ_289969,RMVar_hsa_circ_279315,RMVar_hsa_circ_270820,RMVar_hsa_circ_275877,RMVar_hsa_circ_272882,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_28902,RMVar_hsa_circ_310854,RMVar_hsa_circ_328887,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_123377,RMVar_hsa_circ_106629,RMVar_hsa_circ_108676,RMVar_hsa_circ_87258,RMVar_hsa_circ_258530,RMVar_hsa_circ_258532,RMVar_hsa_circ_258533,RMVar_hsa_circ_258534,RMVar_hsa_circ_258531 13992 RMVar_ID_13992 Human_SNP_ID_411104026 A-to-I Human chr9 - 109049414 109049414 109049414 AGCTCAGGAATTTGACACAACCTGGGCAGCATAGCGAGACCTTGTCTCTACTAAAAATAAAAAAG AGCTCAGGAATTTGACACAACCTGGGCAGCATGGCGAGACCTTGTCTCTACTAAAAATAAAAAAG T C TMEM245 Ensembl:ENSG00000106771 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs12003692 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26606,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_331093,RMVar_hsa_circ_284338,RMVar_hsa_circ_289969,RMVar_hsa_circ_279315,RMVar_hsa_circ_270820,RMVar_hsa_circ_275877,RMVar_hsa_circ_272882,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_28902,RMVar_hsa_circ_310854,RMVar_hsa_circ_328887,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_123377,RMVar_hsa_circ_106629,RMVar_hsa_circ_108676,RMVar_hsa_circ_87258,RMVar_hsa_circ_258530,RMVar_hsa_circ_258532,RMVar_hsa_circ_258533,RMVar_hsa_circ_258534,RMVar_hsa_circ_258531 13993 RMVar_ID_13993 Human_SNP_ID_411104083 A-to-I Human chr9 - 109049616 109049616 109049616 TACCATGTTGGCCAGGCTGGTCTCAAACTCCTAACCTTAAGTGATCTGCCTGCCTCGGCCTCCCA TACCATGTTGGCCAGGCTGGTCTCAAACTCCTCACCTTAAGTGATCTGCCTGCCTCGGCCTCCCA T G TMEM245 Ensembl:ENSG00000106771 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs529073943 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26606,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_331093,RMVar_hsa_circ_284338,RMVar_hsa_circ_289969,RMVar_hsa_circ_279315,RMVar_hsa_circ_270820,RMVar_hsa_circ_275877,RMVar_hsa_circ_272882,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_28902,RMVar_hsa_circ_310854,RMVar_hsa_circ_328887,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_123377,RMVar_hsa_circ_106629,RMVar_hsa_circ_108676,RMVar_hsa_circ_87258,RMVar_hsa_circ_258530,RMVar_hsa_circ_258532,RMVar_hsa_circ_258533,RMVar_hsa_circ_258534,RMVar_hsa_circ_258531 13994 RMVar_ID_13994 Human_SNP_ID_411108116 A-to-I Human chr9 - 109064930 109064930 109064930 ATACAAAATTAGCCAGGCGTGGTGACGTGCCTATGATCTCAGCTACTTGGGAGGCTGAGGCAGGA ATACAAAATTAGCCAGGCGTGGTGACGTGCCTGTGATCTCAGCTACTTGGGAGGCTGAGGCAGGA T C TMEM245 Ensembl:ENSG00000106771 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1428885346 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26197048 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_258514,RMVar_hsa_circ_258516,RMVar_hsa_circ_258517,RMVar_hsa_circ_258515,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_258528,RMVar_hsa_circ_258529,RMVar_hsa_circ_258527,RMVar_hsa_circ_106629,RMVar_hsa_circ_108676,RMVar_hsa_circ_122294,RMVar_hsa_circ_258541,RMVar_hsa_circ_280270,RMVar_hsa_circ_258530,RMVar_hsa_circ_258532,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_258543,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_83182,RMVar_hsa_circ_258554,RMVar_hsa_circ_12019,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_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_31879,RMVar_hsa_circ_258565,RMVar_hsa_circ_339544,RMVar_hsa_circ_348945,RMVar_hsa_circ_729,RMVar_hsa_circ_375724,RMVar_hsa_circ_348718,RMVar_hsa_circ_52591,RMVar_hsa_circ_330961,RMVar_hsa_circ_258566,RMVar_hsa_circ_258567 13995 RMVar_ID_13995 Human_SNP_ID_411108117 A-to-I Human chr9 - 109064930 109064930 109064930 ATACAAAATTAGCCAGGCGTGGTGACGTGCCTATGATCTCAGCTACTTGGGAGGCTGAGGCAGGA ATACAAAATTAGCCAGGCGTGGTGACGTGCCTCTGATCTCAGCTACTTGGGAGGCTGAGGCAGGA T G TMEM245 Ensembl:ENSG00000106771 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1428885346 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26197048 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_258514,RMVar_hsa_circ_258516,RMVar_hsa_circ_258517,RMVar_hsa_circ_258515,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_258528,RMVar_hsa_circ_258529,RMVar_hsa_circ_258527,RMVar_hsa_circ_106629,RMVar_hsa_circ_108676,RMVar_hsa_circ_122294,RMVar_hsa_circ_258541,RMVar_hsa_circ_280270,RMVar_hsa_circ_258530,RMVar_hsa_circ_258532,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_258543,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_83182,RMVar_hsa_circ_258554,RMVar_hsa_circ_12019,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_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_31879,RMVar_hsa_circ_258565,RMVar_hsa_circ_339544,RMVar_hsa_circ_348945,RMVar_hsa_circ_729,RMVar_hsa_circ_375724,RMVar_hsa_circ_348718,RMVar_hsa_circ_52591,RMVar_hsa_circ_330961,RMVar_hsa_circ_258566,RMVar_hsa_circ_258567 13996 RMVar_ID_13996 Human_SNP_ID_411109702 A-to-I Human chr9 - 109071392 109071392 109071392 GTTGCCTAGGCTGGTCTTGAACACCTGGGCTCAAGTGATCTTCCCTCCTCAGCCTCCCGAAGTGC GTTGCCTAGGCTGGTCTTGAACACCTGGGCTCGAGTGATCTTCCCTCCTCAGCCTCCCGAAGTGC T C TMEM245 Ensembl:ENSG00000106771 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1316678115 Functional Loss SNV dbSNP153 33..33 33 - - - 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_258514,RMVar_hsa_circ_258516,RMVar_hsa_circ_258517,RMVar_hsa_circ_258515,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_258528,RMVar_hsa_circ_258529,RMVar_hsa_circ_258527,RMVar_hsa_circ_106629,RMVar_hsa_circ_108676,RMVar_hsa_circ_122294,RMVar_hsa_circ_258541,RMVar_hsa_circ_280270,RMVar_hsa_circ_258530,RMVar_hsa_circ_258532,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_258543,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_83182,RMVar_hsa_circ_258554,RMVar_hsa_circ_12019,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_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_31879,RMVar_hsa_circ_258565,RMVar_hsa_circ_339544,RMVar_hsa_circ_348945,RMVar_hsa_circ_729,RMVar_hsa_circ_375724,RMVar_hsa_circ_348718,RMVar_hsa_circ_52591,RMVar_hsa_circ_330961,RMVar_hsa_circ_258566,RMVar_hsa_circ_258567 13997 RMVar_ID_13997 Human_SNP_ID_411113302 A-to-I Human chr9 - 109085222 109085222 109085222 ACACACTTGTAGTCCTAACTACCCAGGATGCTAGGGCAGAAGGATTGTTTGAGCCCAGGAATTCA ACACACTTGTAGTCCTAACTACCCAGGATGCTGGGGCAGAAGGATTGTTTGAGCCCAGGAATTCA T C TMEM245 Ensembl:ENSG00000106771 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs754622152 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7886799,Human_RBP_ID_16537253,Human_RBP_ID_26565846 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_289969,RMVar_hsa_circ_279315,RMVar_hsa_circ_258514,RMVar_hsa_circ_258516,RMVar_hsa_circ_258515,RMVar_hsa_circ_258513,RMVar_hsa_circ_107760,RMVar_hsa_circ_102086,RMVar_hsa_circ_258528,RMVar_hsa_circ_258529,RMVar_hsa_circ_106629,RMVar_hsa_circ_108676,RMVar_hsa_circ_122294,RMVar_hsa_circ_258530,RMVar_hsa_circ_258531,RMVar_hsa_circ_294617,RMVar_hsa_circ_300656,RMVar_hsa_circ_374311,RMVar_hsa_circ_351398,RMVar_hsa_circ_87627,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_12019,RMVar_hsa_circ_258549,RMVar_hsa_circ_258551,RMVar_hsa_circ_258552,RMVar_hsa_circ_258550,RMVar_hsa_circ_290458,RMVar_hsa_circ_353260,RMVar_hsa_circ_258548,RMVar_hsa_circ_373949,RMVar_hsa_circ_322933,RMVar_hsa_circ_258559,RMVar_hsa_circ_258560,RMVar_hsa_circ_69704,RMVar_hsa_circ_258558,RMVar_hsa_circ_258569,RMVar_hsa_circ_339544,RMVar_hsa_circ_348945,RMVar_hsa_circ_729,RMVar_hsa_circ_375724,RMVar_hsa_circ_52591,RMVar_hsa_circ_258566,RMVar_hsa_circ_258567,RMVar_hsa_circ_98752,RMVar_hsa_circ_274744,RMVar_hsa_circ_304297,RMVar_hsa_circ_272503,RMVar_hsa_circ_258570,RMVar_hsa_circ_258572,RMVar_hsa_circ_281180,RMVar_hsa_circ_327115,RMVar_hsa_circ_258568,RMVar_hsa_circ_353000,RMVar_hsa_circ_284935,RMVar_hsa_circ_258573,RMVar_hsa_circ_258571 13998 RMVar_ID_13998 Human_SNP_ID_411115564 A-to-I Human chr9 - 109093550 109093550 109093550 TACCAGGGCAGGTTATCTCCATGGCAGCTTCTACTCTGGCAAACTTGGCCATCTCTATCACAGGG TACCAGGGCAGGTTATCTCCATGGCAGCTTCTGCTCTGGCAAACTTGGCCATCTCTATCACAGGG T C TMEM245 Ensembl:ENSG00000106771 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1294556948 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_962578,Human_RBP_ID_3975604,Human_RBP_ID_5005524,Human_RBP_ID_16537521,Human_RBP_ID_17320727,Human_RBP_ID_27540967 Human_Splice_Rec_1070142,Human_Splice_Rec_1070143,Human_Splice_Rec_1070202,Human_Splice_Rec_1070203 RMVar_hsa_circ_26606,RMVar_hsa_circ_329834,RMVar_hsa_circ_289969,RMVar_hsa_circ_258514,RMVar_hsa_circ_258513,RMVar_hsa_circ_107760,RMVar_hsa_circ_258529,RMVar_hsa_circ_108676,RMVar_hsa_circ_122294,RMVar_hsa_circ_258530,RMVar_hsa_circ_294617,RMVar_hsa_circ_300656,RMVar_hsa_circ_258537,RMVar_hsa_circ_258536,RMVar_hsa_circ_125084,RMVar_hsa_circ_115756,RMVar_hsa_circ_93834,RMVar_hsa_circ_127919,RMVar_hsa_circ_258549,RMVar_hsa_circ_258551,RMVar_hsa_circ_258550,RMVar_hsa_circ_290458,RMVar_hsa_circ_258548,RMVar_hsa_circ_322933,RMVar_hsa_circ_258559,RMVar_hsa_circ_69704,RMVar_hsa_circ_258558,RMVar_hsa_circ_258569,RMVar_hsa_circ_339544,RMVar_hsa_circ_52591,RMVar_hsa_circ_274744,RMVar_hsa_circ_272503,RMVar_hsa_circ_258570,RMVar_hsa_circ_258572,RMVar_hsa_circ_281180,RMVar_hsa_circ_284935,RMVar_hsa_circ_258573,RMVar_hsa_circ_276372,RMVar_hsa_circ_258574,RMVar_hsa_circ_376579,RMVar_hsa_circ_327653,RMVar_hsa_circ_258576,RMVar_hsa_circ_330318,RMVar_hsa_circ_258575,RMVar_hsa_circ_298570,RMVar_hsa_circ_258579,RMVar_hsa_circ_258581,RMVar_hsa_circ_111476,RMVar_hsa_circ_258580,RMVar_hsa_circ_258582,RMVar_hsa_circ_317262 13999 RMVar_ID_13999 Human_SNP_ID_411118562 A-to-I Human chr9 - 109106168 109106168 109106168 CAGGCTGGAGTGCAGTGGCACAATCATAGCTCACTGTAACCTTGAACTCCTGGGCTCAGGGGTTT CAGGCTGGAGTGCAGTGGCACAATCATAGCTCTCTGTAACCTTGAACTCCTGGGCTCAGGGGTTT T A TMEM245 Ensembl:ENSG00000106771 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1254496186 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_289969,RMVar_hsa_circ_258513,RMVar_hsa_circ_108676,RMVar_hsa_circ_258530,RMVar_hsa_circ_294617,RMVar_hsa_circ_258536,RMVar_hsa_circ_125084,RMVar_hsa_circ_115756,RMVar_hsa_circ_93834,RMVar_hsa_circ_127919,RMVar_hsa_circ_258549,RMVar_hsa_circ_258550,RMVar_hsa_circ_290458,RMVar_hsa_circ_258548,RMVar_hsa_circ_258558,RMVar_hsa_circ_339544,RMVar_hsa_circ_272503,RMVar_hsa_circ_258570,RMVar_hsa_circ_281180,RMVar_hsa_circ_258573,RMVar_hsa_circ_276372,RMVar_hsa_circ_258574,RMVar_hsa_circ_376579,RMVar_hsa_circ_258575,RMVar_hsa_circ_298570,RMVar_hsa_circ_258581,RMVar_hsa_circ_111476,RMVar_hsa_circ_258580,RMVar_hsa_circ_258582,RMVar_hsa_circ_317262 14000 RMVar_ID_14000 Human_SNP_ID_411121051 A-to-I Human chr9 - 109115809 109115809 109115809 TAGTGGATTGTAGGCCAGGTGCGGTTGCTCACACCTGTAATCCCAGCACTTTGGGAAGCCGAGGC TAGTGGATTGTAGGCCAGGTGCGGTTGCTCACGCCTGTAATCCCAGCACTTTGGGAAGCCGAGGC T C TMEM245 Ensembl:ENSG00000106771 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1210671191 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_182657 RMVar_hsa_circ_93834,RMVar_hsa_circ_258548,RMVar_hsa_circ_107228,RMVar_hsa_circ_258581,RMVar_hsa_circ_111476,RMVar_hsa_circ_258584 14001 RMVar_ID_14001 Human_SNP_ID_411132244 A-to-I Human chr9 - 109160576 109160576 109160576 TGAGATCAGCTTGGGCAAGAAAGTGATACCCCATCTCTACAAAAAGATAAAAAAGTTAGCCAGTC TGAGATCAGCTTGGGCAAGAAAGTGATACCCCGTCTCTACAAAAAGATAAAAAAGTTAGCCAGTC T C FRRS1L Ensembl:ENSG00000260230 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1293392772 Functional Loss SNV dbSNP153 33..33 33 - - - 14002 RMVar_ID_14002 Human_SNP_ID_411132349 A-to-I Human chr9 - 109160961 109160961 109160961 CATGGTGAAACCTGTCTCTACAAAAATACAAAAATTAGCCGGGCATGATGGCGGGTGCCTGTAAT CATGGTGAAACCTGTCTCTACAAAAATACAAATATTAGCCGGGCATGATGGCGGGTGCCTGTAAT T A FRRS1L Ensembl:ENSG00000260230 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1330389658 Functional Loss SNV dbSNP153 33..33 33 - - - 14003 RMVar_ID_14003 Human_SNP_ID_411146027 A-to-I Human chr9 - 109217751 109217751 109217751 CCAGGCAACATAGCGAGATCCTGTCTCTACAAAAAATTTTAAAAATTAGCCAGGCATGGTGTCAT CCAGGCAACATAGCGAGATCCTGTCTCTACAAGAAATTTTAAAAATTAGCCAGGCATGGTGTCAT T C EPB41L4B Ensembl:ENSG00000095203 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs192292368 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112898,RMVar_hsa_circ_258596,RMVar_hsa_circ_41316,RMVar_hsa_circ_264968 14004 RMVar_ID_14004 Human_SNP_ID_411398190 A-to-I Human chr9 - 110246027 110246027 110246027 ATAGTCTCATTCTGTCGCCCAGGCTGGAATACAGTGGCATGATCTCAGCTCACTGCAACCTCCGC ATAGTCTCATTCTGTCGCCCAGGCTGGAATACGGTGGCATGATCTCAGCTCACTGCAACCTCCGC T C TXN Ensembl:ENSG00000136810 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1219038036 Functional Loss SNV dbSNP153 33..33 33 - - - 14005 RMVar_ID_14005 Human_SNP_ID_411398462 A-to-I Human chr9 - 110247223 110247223 110247223 CACCTCCCGGGTTCAAGCGATTCTTCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCAGCCG CACCTCCCGGGTTCAAGCGATTCTTCTGCCTCGGCCTCCTGAGTAGCTGGGACTACAGGCAGCCG T C TXN Ensembl:ENSG00000136810 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs753979577 Functional Loss SNV dbSNP153 33..33 33 - - - 14006 RMVar_ID_14006 Human_SNP_ID_411399801 A-to-I Human chr9 - 110252058 110252058 110252058 CACCACGCCCAGCTAGTTTCTGTATTTTTAGTAGAGACAGCATTTCACCATATTGGCCAGGCTGG CACCACGCCCAGCTAGTTTCTGTATTTTTAGTGGAGACAGCATTTCACCATATTGGCCAGGCTGG T C TXN Ensembl:ENSG00000136810 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs925836349 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26197464 14007 RMVar_ID_14007 Human_SNP_ID_411399816 A-to-I Human chr9 - 110252137 110252137 110252137 TCACTGCAACCTCCGCCTCCTGAGTTCAAGCTATTCTCCTGCCTCAGCCTCCTGAGTGGCTGGGA TCACTGCAACCTCCGCCTCCTGAGTTCAAGCTGTTCTCCTGCCTCAGCCTCCTGAGTGGCTGGGA T C TXN Ensembl:ENSG00000136810 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs186088435 Functional Loss SNV dbSNP153 33..33 33 - - - 14008 RMVar_ID_14008 Human_SNP_ID_411399817 A-to-I Human chr9 - 110252137 110252137 110252137 TCACTGCAACCTCCGCCTCCTGAGTTCAAGCTATTCTCCTGCCTCAGCCTCCTGAGTGGCTGGGA TCACTGCAACCTCCGCCTCCTGAGTTCAAGCTCTTCTCCTGCCTCAGCCTCCTGAGTGGCTGGGA T G TXN Ensembl:ENSG00000136810 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs186088435 Functional Loss SNV dbSNP153 33..33 33 - - - 14009 RMVar_ID_14009 Human_SNP_ID_411400019 A-to-I Human chr9 - 110252730 110252730 110252730 TGAGGCAAGAGAATCACTTGAACCCCGGAGGCAAAGGTTACTGTGAGCCGAGATCAGGCCTTTGC TGAGGCAAGAGAATCACTTGAACCCCGGAGGCCAAGGTTACTGTGAGCCGAGATCAGGCCTTTGC T G TXN Ensembl:ENSG00000136810 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1321317051 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16538839 14010 RMVar_ID_14010 Human_SNP_ID_411400034 A-to-I Human chr9 - 110252782 110252782 110252782 AAATTAGCTGGGACTGGTGGCAGAGGCTTGTAATCCCAGCTACTCAGGAGGCTGAGGCAAGAGAA AAATTAGCTGGGACTGGTGGCAGAGGCTTGTATTCCCAGCTACTCAGGAGGCTGAGGCAAGAGAA T A TXN Ensembl:ENSG00000136810 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1189464713 Functional Loss SNV dbSNP153 33..33 33 - - - 14011 RMVar_ID_14011 Human_SNP_ID_411400035 A-to-I Human chr9 - 110252782 110252782 110252782 AAATTAGCTGGGACTGGTGGCAGAGGCTTGTAATCCCAGCTACTCAGGAGGCTGAGGCAAGAGAA AAATTAGCTGGGACTGGTGGCAGAGGCTTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAAGAGAA T C TXN Ensembl:ENSG00000136810 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1189464713 Functional Loss SNV dbSNP153 33..33 33 - - - 14012 RMVar_ID_14012 Human_SNP_ID_411400044 A-to-I Human chr9 - 110252824 110252824 110252824 CCTGGTCAACATGGCGAAACTCTGTCTCTACTAAAAATACAAAAATTAGCTGGGACTGGTGGCAG CCTGGTCAACATGGCGAAACTCTGTCTCTACTGAAAATACAAAAATTAGCTGGGACTGGTGGCAG T C TXN Ensembl:ENSG00000136810 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1245197446 Functional Loss SNV dbSNP153 33..33 33 - - - 14013 RMVar_ID_14013 Human_SNP_ID_411400049 A-to-I Human chr9 - 110252846 110252846 110252846 CAGGTCAGGAGTTCAAGACCAGCCTGGTCAACATGGCGAAACTCTGTCTCTACTAAAAATACAAA CAGGTCAGGAGTTCAAGACCAGCCTGGTCAACTTGGCGAAACTCTGTCTCTACTAAAAATACAAA T A TXN Ensembl:ENSG00000136810 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1040133980 Functional Loss SNV dbSNP153 33..33 33 - - - 14014 RMVar_ID_14014 Human_SNP_ID_411439289 A-to-I Human chr9 - 110401729 110401726 110401730 AATTTTTCAATAGTGTAGGTAGTGCCTTAATAATTTTTTTTTGCAGAAATCTTTCTGGGTAATGA AATTTTTCAATAGTGTAGGTAGTGCCTTAAT____TTTTTTTGCAGAAATCTTTCTGGGTAATGA AAATT A SVEP1 Ensembl:ENSG00000165124 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1564131650 Functional Loss DEL dbSNP153 32..35 33 - - - RMVar_hsa_circ_119189,RMVar_hsa_circ_268092,RMVar_hsa_circ_258621,RMVar_hsa_circ_266982,RMVar_hsa_circ_365414,RMVar_hsa_circ_288867,RMVar_hsa_circ_356997,RMVar_hsa_circ_258622 14015 RMVar_ID_14015 Human_SNP_ID_411439290 A-to-I Human chr9 - 110401729 110401727 110401730 AATTTTTCAATAGTGTAGGTAGTGCCTTAATAATTTTTTTTTGCAGAAATCTTTCTGGGTAATGA AATTTTTCAATAGTGTAGGTAGTGCCTTAAT___TTTTTTTTGCAGAAATCTTTCTGGGTAATGA AATT A SVEP1 Ensembl:ENSG00000165124 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1280240663 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_119189,RMVar_hsa_circ_268092,RMVar_hsa_circ_258621,RMVar_hsa_circ_266982,RMVar_hsa_circ_365414,RMVar_hsa_circ_288867,RMVar_hsa_circ_356997,RMVar_hsa_circ_258622 14016 RMVar_ID_14016 Human_SNP_ID_411462734 A-to-I Human chr9 - 110494155 110494155 110494155 CTAATCCCTAGAACCTGCAAATATGTTTCCTTACATAGCAAAGGAACTTTGTAGATGTGATGAAA CTAATCCCTAGAACCTGCAAATATGTTTCCTTTCATAGCAAAGGAACTTTGTAGATGTGATGAAA T A SVEP1 Ensembl:ENSG00000165124 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1033949207 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29087,RMVar_hsa_circ_55630,RMVar_hsa_circ_54431,RMVar_hsa_circ_12583,RMVar_hsa_circ_349475,RMVar_hsa_circ_34394,RMVar_hsa_circ_59211,RMVar_hsa_circ_258628 14017 RMVar_ID_14017 Human_SNP_ID_411673109 A-to-I Human chr9 - 111355837 111355837 111355837 GTATGTCAATGTAAGTTCATCAGTTGCAACCAACTTACCACTATGGTACAAGATGTTGACAGTGG GTATGTCAATGTAAGTTCATCAGTTGCAACCAGCTTACCACTATGGTACAAGATGTTGACAGTGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1391554441 Functional Loss SNV dbSNP153 33..33 33 - - - 14018 RMVar_ID_14018 Human_SNP_ID_411682069 A-to-I Human chr9 - 111390084 111390084 111390084 TTCTTTGTTTCCAAGTCAGGGCCTTTCTACTTACAAGGAACTTTGTTCTCTGGCAAGTGATCTTA TTCTTTGTTTCCAAGTCAGGGCCTTTCTACTTGCAAGGAACTTTGTTCTCTGGCAAGTGATCTTA T C ECPAS Ensembl:ENSG00000136813 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs760559326 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1402188,Human_RBP_ID_18394718,Human_RBP_ID_26239585 Human_Splice_Rec_1071210,Human_Splice_Rec_1071310 RMVar_hsa_circ_66103,RMVar_hsa_circ_258653,RMVar_hsa_circ_123308,RMVar_hsa_circ_269384,RMVar_hsa_circ_120555,RMVar_hsa_circ_258652,RMVar_hsa_circ_60249,RMVar_hsa_circ_18182,RMVar_hsa_circ_125154,RMVar_hsa_circ_12118,RMVar_hsa_circ_26326,RMVar_hsa_circ_84724,RMVar_hsa_circ_258660,RMVar_hsa_circ_376675,RMVar_hsa_circ_106289,RMVar_hsa_circ_109510,RMVar_hsa_circ_71534,RMVar_hsa_circ_258662,RMVar_hsa_circ_126122,RMVar_hsa_circ_121072,RMVar_hsa_circ_258663,RMVar_hsa_circ_258664,RMVar_hsa_circ_258665,RMVar_hsa_circ_258666,RMVar_hsa_circ_101638,RMVar_hsa_circ_258668,RMVar_hsa_circ_24345,RMVar_hsa_circ_121976,RMVar_hsa_circ_258669,RMVar_hsa_circ_117768,RMVar_hsa_circ_123255,RMVar_hsa_circ_258670,RMVar_hsa_circ_101527,RMVar_hsa_circ_258671,RMVar_hsa_circ_258672,RMVar_hsa_circ_80828,RMVar_hsa_circ_74846,RMVar_hsa_circ_91080,RMVar_hsa_circ_125778,RMVar_hsa_circ_258673,RMVar_hsa_circ_115679,RMVar_hsa_circ_83507,RMVar_hsa_circ_39847,RMVar_hsa_circ_258674,RMVar_hsa_circ_258676,RMVar_hsa_circ_258677,RMVar_hsa_circ_258675,RMVar_hsa_circ_371636,RMVar_hsa_circ_258678,RMVar_hsa_circ_116529,RMVar_hsa_circ_97675,RMVar_hsa_circ_258681,RMVar_hsa_circ_275279,RMVar_hsa_circ_36601,RMVar_hsa_circ_83719,RMVar_hsa_circ_26656,RMVar_hsa_circ_72091,RMVar_hsa_circ_96204,RMVar_hsa_circ_258682,RMVar_hsa_circ_258683,RMVar_hsa_circ_105654,RMVar_hsa_circ_78243,RMVar_hsa_circ_258686,RMVar_hsa_circ_258687,RMVar_hsa_circ_258685,RMVar_hsa_circ_27563,RMVar_hsa_circ_332642,RMVar_hsa_circ_103753,RMVar_hsa_circ_270031,RMVar_hsa_circ_258688,RMVar_hsa_circ_355481,RMVar_hsa_circ_106623,RMVar_hsa_circ_85499,RMVar_hsa_circ_100196,RMVar_hsa_circ_84572,RMVar_hsa_circ_25860,RMVar_hsa_circ_258691,RMVar_hsa_circ_258693,RMVar_hsa_circ_258694,RMVar_hsa_circ_258695,RMVar_hsa_circ_258692,RMVar_hsa_circ_258689,RMVar_hsa_circ_258690,RMVar_hsa_circ_97533,RMVar_hsa_circ_318829,RMVar_hsa_circ_258696 14019 RMVar_ID_14019 Human_SNP_ID_411702635 A-to-I Human chr9 - 111470491 111470491 111470491 CACGGGTAACACAGTGAAACCCCATCTCTACTAAAAATACAAAAAGTTAGCTGGGTGTCGTGGCA CACGGGTAACACAGTGAAACCCCATCTCTACTGAAAATACAAAAAGTTAGCTGGGTGTCGTGGCA T C ECPAS Ensembl:ENSG00000136813 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs372479313 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,RMVar_hsa_circ_268992,RMVar_hsa_circ_258727,RMVar_hsa_circ_319053,RMVar_hsa_circ_258730,RMVar_hsa_circ_304098 14020 RMVar_ID_14020 Human_SNP_ID_411703545 A-to-I Human chr9 - 111473867 111473867 111473867 AATTTCCTGGTCTCAATCCATCTTCTGACCTCAGCCTCCTGAGTAGCTGGGACTGCAGGCGGGTA AATTTCCTGGTCTCAATCCATCTTCTGACCTCGGCCTCCTGAGTAGCTGGGACTGCAGGCGGGTA T C ECPAS Ensembl:ENSG00000136813 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1184645670 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,RMVar_hsa_circ_114298,RMVar_hsa_circ_258731 14021 RMVar_ID_14021 Human_SNP_ID_411719257 A-to-I Human chr9 + 111533499 111533499 111533499 AGCCCAAGAGTTTGAGACCAGCCTGGGCAAATAGTGAGACAATGCCTCTACAAAAAATTTAAAAA AGCCCAAGAGTTTGAGACCAGCCTGGGCAAATCGTGAGACAATGCCTCTACAAAAAATTTAAAAA A C ZNF483 Ensembl:ENSG00000173258 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1272041953 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_272093,RMVar_hsa_circ_267205,RMVar_hsa_circ_258733,RMVar_hsa_circ_258734,RMVar_hsa_circ_308979 14022 RMVar_ID_14022 Human_SNP_ID_411719861 A-to-I Human chr9 + 111535673 111535673 111535673 TCAAGTGATTCTCTTGCCTCGGCCTCCCAAGTAGCTGGGACTACAAGCATGTGCCACCACGCCAA TCAAGTGATTCTCTTGCCTCGGCCTCCCAAGTTGCTGGGACTACAAGCATGTGCCACCACGCCAA A T ZNF483 Ensembl:ENSG00000173258 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1203592886 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267205 14023 RMVar_ID_14023 Human_SNP_ID_411720385 A-to-I Human chr9 + 111537402 111537402 111537402 CACCACCATGCCCAGCTAAATTTTGTATTTTCAGTAGAGACGGGGTTTAACCATGTTGATCTCGA CACCACCATGCCCAGCTAAATTTTGTATTTTCGGTAGAGACGGGGTTTAACCATGTTGATCTCGA A G ZNF483 Ensembl:ENSG00000173258 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1168568958 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267205 14024 RMVar_ID_14024 Human_SNP_ID_411725544 A-to-I Human chr9 - 111557964 111557964 111557964 TTTTGTATTTTTAGTAGAGACAGAGTTTCACTATTTTGGCCAGGCTGGCCTCGAACTCTTAACCT TTTTGTATTTTTAGTAGAGACAGAGTTTCACTGTTTTGGCCAGGCTGGCCTCGAACTCTTAACCT T C PTGR1 Ensembl:ENSG00000106853 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1034915953 Functional Loss SNV dbSNP153 33..33 33 - - - 14025 RMVar_ID_14025 Human_SNP_ID_411727708 A-to-I Human chr9 - 111565002 111565002 111565002 CTTCTGCCTCAGCCTCCTGACTAGCTGGGATTACAGGTACACGCCACCACGCCTGGCTAATTTTC CTTCTGCCTCAGCCTCCTGACTAGCTGGGATTGCAGGTACACGCCACCACGCCTGGCTAATTTTC T C PTGR1 Ensembl:ENSG00000106853 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1297009287 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100335,RMVar_hsa_circ_354338,RMVar_hsa_circ_258738,RMVar_hsa_circ_357363 14026 RMVar_ID_14026 Human_SNP_ID_411727739 A-to-I Human chr9 - 111565085 111565085 111565085 AGTTTTGCTCTTGTTGCCCAGGCTGGGGTGCAATGGTGCGATCTCCGTTCACTGCAACCTCCGCC AGTTTTGCTCTTGTTGCCCAGGCTGGGGTGCAGTGGTGCGATCTCCGTTCACTGCAACCTCCGCC T C PTGR1 Ensembl:ENSG00000106853 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985935027 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100335,RMVar_hsa_circ_354338,RMVar_hsa_circ_258738,RMVar_hsa_circ_357363 14027 RMVar_ID_14027 Human_SNP_ID_411728150 A-to-I Human chr9 - 111566989 111566989 111566989 CTTGACCCAGGCTCAGGGGATTCTCCCACCTCAACCTCCTGAGTAGCTGGGACAACAGTCATGTG CTTGACCCAGGCTCAGGGGATTCTCCCACCTCGACCTCCTGAGTAGCTGGGACAACAGTCATGTG T C PTGR1 Ensembl:ENSG00000106853 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1262797745 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100335,RMVar_hsa_circ_354338,RMVar_hsa_circ_258738,RMVar_hsa_circ_357363 14028 RMVar_ID_14028 Human_SNP_ID_411733566 A-to-I Human chr9 - 111590483 111590483 111590483 GTGGTGATGGGCATCTGTAATCCTAGCTATTCAGGAGGCTGAGGCATGAGAATTGCTTGAACCCA GTGGTGATGGGCATCTGTAATCCTAGCTATTCGGGAGGCTGAGGCATGAGAATTGCTTGAACCCA T C PTGR1 Ensembl:ENSG00000106853 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1211516017 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48070,RMVar_hsa_circ_351321,RMVar_hsa_circ_347804,RMVar_hsa_circ_258739,RMVar_hsa_circ_333897,RMVar_hsa_circ_361016,RMVar_hsa_circ_353441,RMVar_hsa_circ_331329,RMVar_hsa_circ_357371,RMVar_hsa_circ_353363,RMVar_hsa_circ_332381 14029 RMVar_ID_14029 Human_SNP_ID_411733597 A-to-I Human chr9 - 111590605 111590605 111590605 CCTGTAATCCCAGCATTTTGGGAGGCTGAAGCAGGAGGATCACTTGAGGTCAGGAATTTGAGACC CCTGTAATCCCAGCATTTTGGGAGGCTGAAGCGGGAGGATCACTTGAGGTCAGGAATTTGAGACC T C PTGR1 Ensembl:ENSG00000106853 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs755146476 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48070,RMVar_hsa_circ_351321,RMVar_hsa_circ_347804,RMVar_hsa_circ_258739,RMVar_hsa_circ_333897,RMVar_hsa_circ_361016,RMVar_hsa_circ_353441,RMVar_hsa_circ_331329,RMVar_hsa_circ_357371,RMVar_hsa_circ_353363,RMVar_hsa_circ_332381 14030 RMVar_ID_14030 Human_SNP_ID_411733714 A-to-I Human chr9 - 111591169 111591169 111591169 CTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCATGCACCACCGCACCCGGCTAATTTTG CTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTGCAGGCATGCACCACCGCACCCGGCTAATTTTG T C PTGR1 Ensembl:ENSG00000106853 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1463928233 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48070,RMVar_hsa_circ_351321,RMVar_hsa_circ_347804,RMVar_hsa_circ_258739,RMVar_hsa_circ_333897,RMVar_hsa_circ_361016,RMVar_hsa_circ_353441,RMVar_hsa_circ_331329,RMVar_hsa_circ_357371,RMVar_hsa_circ_353363,RMVar_hsa_circ_332381 14031 RMVar_ID_14031 Human_SNP_ID_411733717 A-to-I Human chr9 - 111591179 111591179 111591179 GATTCTGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCATGCACCACCGCACCCG GATTCTGATTCTCCTGCCTCAGCCTCCCAAGTGGCTGGGATTACAGGCATGCACCACCGCACCCG T C PTGR1 Ensembl:ENSG00000106853 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1415619904 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48070,RMVar_hsa_circ_351321,RMVar_hsa_circ_347804,RMVar_hsa_circ_258739,RMVar_hsa_circ_333897,RMVar_hsa_circ_361016,RMVar_hsa_circ_353441,RMVar_hsa_circ_331329,RMVar_hsa_circ_357371,RMVar_hsa_circ_353363,RMVar_hsa_circ_332381 14032 RMVar_ID_14032 Human_SNP_ID_411733835 A-to-I Human chr9 - 111591534 111591534 111591534 GAAACCCCGTCTCTACTAAAAAAACAAAAATTAACTGGGTGTGGTAGTGCATGCCTGTAATCCCA GAAACCCCGTCTCTACTAAAAAAACAAAAATTGACTGGGTGTGGTAGTGCATGCCTGTAATCCCA T C PTGR1 Ensembl:ENSG00000106853 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1179005654 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48070,RMVar_hsa_circ_351321,RMVar_hsa_circ_347804,RMVar_hsa_circ_258739,RMVar_hsa_circ_333897,RMVar_hsa_circ_361016,RMVar_hsa_circ_353441,RMVar_hsa_circ_331329,RMVar_hsa_circ_357371,RMVar_hsa_circ_353363,RMVar_hsa_circ_332381 14033 RMVar_ID_14033 Human_SNP_ID_411733849 A-to-I Human chr9 - 111591583 111591583 111591583 GGCAGTTCACTTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCCGTCTCTAC GGCAGTTCACTTGAGGTCAGGAGTTCGAGACCTGCCTGGCCAACATGGTGAAACCCCGTCTCTAC T A PTGR1 Ensembl:ENSG00000106853 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1007322660 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48070,RMVar_hsa_circ_351321,RMVar_hsa_circ_347804,RMVar_hsa_circ_258739,RMVar_hsa_circ_333897,RMVar_hsa_circ_361016,RMVar_hsa_circ_353441,RMVar_hsa_circ_331329,RMVar_hsa_circ_357371,RMVar_hsa_circ_353363,RMVar_hsa_circ_332381 14034 RMVar_ID_14034 Human_SNP_ID_411733854 A-to-I Human chr9 - 111591597 111591597 111591597 GGGAAGCTGAGGTGGGCAGTTCACTTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGA GGGAAGCTGAGGTGGGCAGTTCACTTGAGGTCCGGAGTTCGAGACCAGCCTGGCCAACATGGTGA T G PTGR1 Ensembl:ENSG00000106853 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1159184291 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48070,RMVar_hsa_circ_351321,RMVar_hsa_circ_347804,RMVar_hsa_circ_258739,RMVar_hsa_circ_333897,RMVar_hsa_circ_361016,RMVar_hsa_circ_353441,RMVar_hsa_circ_331329,RMVar_hsa_circ_357371,RMVar_hsa_circ_353363,RMVar_hsa_circ_332381 14035 RMVar_ID_14035 Human_SNP_ID_411749732 A-to-I Human chr9 + 111651609 111651609 111651609 TGACAGCATTAAAAGTTACAGAATTGCAGGCTAGGTGCGGTGGCTCATGCCTGTAATCCCAGCAC TGACAGCATTAAAAGTTACAGAATTGCAGGCTGGGTGCGGTGGCTCATGCCTGTAATCCCAGCAC A G DNAJC25-GNG10,DNAJC25 Ensembl:ENSG00000244115,Ensembl:ENSG00000059769 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs181095544 Functional Loss SNV dbSNP153 33..33 33 - - - 14036 RMVar_ID_14036 Human_SNP_ID_411770471 A-to-I Human chr9 + 111747832 111747832 111747832 GTCTTGAACTCTTGATCTTAAGTGATCCGCCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGC GTCTTGAACTCTTGATCTTAAGTGATCCGCCCCCCTCAGCCTCCCAAAGTGCTGGGATTACAGGC A C HSALNG0073712 RNACentral:URS0000EB67F4 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs945829949 Functional Loss SNV dbSNP153 33..33 33 - - - 14037 RMVar_ID_14037 Human_SNP_ID_411806722 A-to-I Human chr9 + 111904801 111904801 111904801 GGAGAATCACTTGAACTCGGGAGGTGGAGGTTACAGTGAGCCAAGGTTGTGCCATTGCTCTCCAG GGAGAATCACTTGAACTCGGGAGGTGGAGGTTGCAGTGAGCCAAGGTTGTGCCATTGCTCTCCAG A G UGCG Ensembl:ENSG00000148154 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1213728234 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86759,RMVar_hsa_circ_258744 14038 RMVar_ID_14038 Human_SNP_ID_411809823 A-to-I Human chr9 + 111916666 111916666 111916666 TGATTTTTGTATTTTTTGTAGAGGGTGTTGCCATGTTGCCGGGGCTGGTCTTGAACTCTTGGGCT TGATTTTTGTATTTTTTGTAGAGGGTGTTGCCGTGTTGCCGGGGCTGGTCTTGAACTCTTGGGCT A G UGCG Ensembl:ENSG00000148154 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1564201469 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16542445 RMVar_hsa_circ_258746,RMVar_hsa_circ_295902,RMVar_hsa_circ_86759,RMVar_hsa_circ_320202,RMVar_hsa_circ_258744,RMVar_hsa_circ_349826,RMVar_hsa_circ_315650,RMVar_hsa_circ_258747,RMVar_hsa_circ_258748,RMVar_hsa_circ_258749 14039 RMVar_ID_14039 Human_SNP_ID_411809839 A-to-I Human chr9 + 111916713 111916713 111916713 GTCTTGAACTCTTGGGCTCAAGCAATCCCCCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGAC GTCTTGAACTCTTGGGCTCAAGCAATCCCCCCCCCTCAGCCTCCCAAAGTGCTGGGATTACAGAC A C UGCG Ensembl:ENSG00000148154 Protein coding intron GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs946327626 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_258746,RMVar_hsa_circ_295902,RMVar_hsa_circ_86759,RMVar_hsa_circ_320202,RMVar_hsa_circ_258744,RMVar_hsa_circ_349826,RMVar_hsa_circ_315650,RMVar_hsa_circ_258747,RMVar_hsa_circ_258748,RMVar_hsa_circ_258749 14040 RMVar_ID_14040 Human_SNP_ID_411810165 A-to-I Human chr9 + 111918061 111918061 111918061 CAATTATAGAATTGATTTTTTTTTTCCTTTTGAGGCAGAGTCTTGCTCTGTCACCTGTGCTGGAG CAATTATAGAATTGATTTTTTTTTTCCTTTTGGGGCAGAGTCTTGCTCTGTCACCTGTGCTGGAG A G UGCG Ensembl:ENSG00000148154 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs534836808 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16542465 RMVar_hsa_circ_295902,RMVar_hsa_circ_86759,RMVar_hsa_circ_320202,RMVar_hsa_circ_258744,RMVar_hsa_circ_349826,RMVar_hsa_circ_315650,RMVar_hsa_circ_258747,RMVar_hsa_circ_258748,RMVar_hsa_circ_258749 14041 RMVar_ID_14041 Human_SNP_ID_411810173 A-to-I Human chr9 + 111918095 111918095 111918095 GCAGAGTCTTGCTCTGTCACCTGTGCTGGAGTACAATGCCACAATCTCGGCTCACTGCCACTTCC GCAGAGTCTTGCTCTGTCACCTGTGCTGGAGTGCAATGCCACAATCTCGGCTCACTGCCACTTCC A G UGCG Ensembl:ENSG00000148154 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs578134038 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_295902,RMVar_hsa_circ_86759,RMVar_hsa_circ_320202,RMVar_hsa_circ_258744,RMVar_hsa_circ_349826,RMVar_hsa_circ_315650,RMVar_hsa_circ_258747,RMVar_hsa_circ_258748,RMVar_hsa_circ_258749 14042 RMVar_ID_14042 Human_SNP_ID_411810175 A-to-I Human chr9 + 111918105 111918105 111918105 GCTCTGTCACCTGTGCTGGAGTACAATGCCACAATCTCGGCTCACTGCCACTTCCGCCTCCCGGG GCTCTGTCACCTGTGCTGGAGTACAATGCCACCATCTCGGCTCACTGCCACTTCCGCCTCCCGGG A C UGCG Ensembl:ENSG00000148154 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1352729449 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_295902,RMVar_hsa_circ_86759,RMVar_hsa_circ_320202,RMVar_hsa_circ_258744,RMVar_hsa_circ_349826,RMVar_hsa_circ_315650,RMVar_hsa_circ_258747,RMVar_hsa_circ_258748,RMVar_hsa_circ_258749 14043 RMVar_ID_14043 Human_SNP_ID_411810203 A-to-I Human chr9 + 111918170 111918170 111918170 TTCAAGCAATTCTCCCGTGTCAGCCTCCCGAGAAGTTGGGATTACAGGCGCATGCCACTACCGCT TTCAAGCAATTCTCCCGTGTCAGCCTCCCGAGCAGTTGGGATTACAGGCGCATGCCACTACCGCT A C UGCG Ensembl:ENSG00000148154 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1484071036 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_295902,RMVar_hsa_circ_86759,RMVar_hsa_circ_320202,RMVar_hsa_circ_258744,RMVar_hsa_circ_349826,RMVar_hsa_circ_315650,RMVar_hsa_circ_258747,RMVar_hsa_circ_258748,RMVar_hsa_circ_258749 14044 RMVar_ID_14044 Human_SNP_ID_411810573 A-to-I Human chr9 + 111919360 111919360 111919360 CAAAAATTAGCCAGGTGTGGTGGTGCACACCTATAGTCCCAGCTACTCGGGAGGCTGAGGTGGGA CAAAAATTAGCCAGGTGTGGTGGTGCACACCTGTAGTCCCAGCTACTCGGGAGGCTGAGGTGGGA A G UGCG Ensembl:ENSG00000148154 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1217161842 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_295902,RMVar_hsa_circ_86759,RMVar_hsa_circ_320202,RMVar_hsa_circ_258744,RMVar_hsa_circ_349826,RMVar_hsa_circ_315650,RMVar_hsa_circ_258747,RMVar_hsa_circ_258748,RMVar_hsa_circ_258749 14045 RMVar_ID_14045 Human_SNP_ID_411810624 A-to-I Human chr9 + 111919520 111919520 111919520 AAACCATTAAAGATACTATGCTGGCTGGGCACAGTGGCTCACACCTGTAATCCCAGCACTCTGGG AAACCATTAAAGATACTATGCTGGCTGGGCACCGTGGCTCACACCTGTAATCCCAGCACTCTGGG A C UGCG Ensembl:ENSG00000148154 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs997169457 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8694542 RMVar_hsa_circ_295902,RMVar_hsa_circ_86759,RMVar_hsa_circ_320202,RMVar_hsa_circ_258744,RMVar_hsa_circ_349826,RMVar_hsa_circ_315650,RMVar_hsa_circ_258747,RMVar_hsa_circ_258748,RMVar_hsa_circ_258749 14046 RMVar_ID_14046 Human_SNP_ID_411810650 A-to-I Human chr9 + 111919608 111919608 111919608 GGTCAGGAGATTGAGACCATCCTGGCTAGCACAGTGAAACTCCGTCTCTACTAAAGAAAAATACA GGTCAGGAGATTGAGACCATCCTGGCTAGCACGGTGAAACTCCGTCTCTACTAAAGAAAAATACA A G UGCG Ensembl:ENSG00000148154 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1490621921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_183277 RMVar_hsa_circ_295902,RMVar_hsa_circ_86759,RMVar_hsa_circ_320202,RMVar_hsa_circ_258744,RMVar_hsa_circ_349826,RMVar_hsa_circ_315650,RMVar_hsa_circ_258747,RMVar_hsa_circ_258748,RMVar_hsa_circ_258749 14047 RMVar_ID_14047 Human_SNP_ID_411810902 A-to-I Human chr9 + 111920565 111920565 111920565 TATTGCATTTTTAGTAGAGACGGGGTTTCACCATGTTGGTCAGGCTGGCCTCGAACTCCTGACCT TATTGCATTTTTAGTAGAGACGGGGTTTCACCGTGTTGGTCAGGCTGGCCTCGAACTCCTGACCT A G UGCG Ensembl:ENSG00000148154 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs943561116 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_295902,RMVar_hsa_circ_86759,RMVar_hsa_circ_320202,RMVar_hsa_circ_258744,RMVar_hsa_circ_349826,RMVar_hsa_circ_315650,RMVar_hsa_circ_258747,RMVar_hsa_circ_258748,RMVar_hsa_circ_258749 14048 RMVar_ID_14048 Human_SNP_ID_411811042 A-to-I Human chr9 + 111921093 111921092 111921094 CTTGGCTAATTTTTCGTATTTTTAGGAGAAACAGGGTTTCACCATGTTTCCCAGGCTGGTCTCAA CTTGGCTAATTTTTCGTATTTTTAGGAGAAAC__GGTTTCACCATGTTTCCCAGGCTGGTCTCAA CAG C UGCG Ensembl:ENSG00000148154 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1448383753 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_295902,RMVar_hsa_circ_86759,RMVar_hsa_circ_320202,RMVar_hsa_circ_258744,RMVar_hsa_circ_349826,RMVar_hsa_circ_315650,RMVar_hsa_circ_258747,RMVar_hsa_circ_258748,RMVar_hsa_circ_258749 14049 RMVar_ID_14049 Human_SNP_ID_411811164 A-to-I Human chr9 + 111921571 111921571 111921571 TGTTTGGGAGGCTGAGGCAGGCGAATCGATTGAACCTGGGAGGCGGAGGTTGCAGTGAGCTGAGA TGTTTGGGAGGCTGAGGCAGGCGAATCGATTGGACCTGGGAGGCGGAGGTTGCAGTGAGCTGAGA A G UGCG Ensembl:ENSG00000148154 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1469689313 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_295902,RMVar_hsa_circ_86759,RMVar_hsa_circ_320202,RMVar_hsa_circ_258744,RMVar_hsa_circ_349826,RMVar_hsa_circ_315650,RMVar_hsa_circ_258747,RMVar_hsa_circ_258748,RMVar_hsa_circ_258749 14050 RMVar_ID_14050 Human_SNP_ID_411811334 A-to-I Human chr9 + 111921951 111921951 111921951 CTCCCACCTCAGCCTCCCAAGTAGCTGGGACCACAGGCATGCCTCACCATGCCCAGCTAATTTTA CTCCCACCTCAGCCTCCCAAGTAGCTGGGACCGCAGGCATGCCTCACCATGCCCAGCTAATTTTA A G UGCG Ensembl:ENSG00000148154 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1313334155 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_295902,RMVar_hsa_circ_86759,RMVar_hsa_circ_320202,RMVar_hsa_circ_258744,RMVar_hsa_circ_349826,RMVar_hsa_circ_315650,RMVar_hsa_circ_258747,RMVar_hsa_circ_258748,RMVar_hsa_circ_258749 14051 RMVar_ID_14051 Human_SNP_ID_411840812 A-to-I Human chr9 - 112036040 112036040 112036040 GGACTACAGATGCGTGCCACCACACCTGACTAATCTTTATATTTTTAGTAGAGAGGGGGGTTTCA GGACTACAGATGCGTGCCACCACACCTGACTACTCTTTATATTTTTAGTAGAGAGGGGGGTTTCA T G AL138756.1 Ensembl:ENSG00000259953 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs112846621 Functional Loss SNV dbSNP153 33..33 33 - - - 14052 RMVar_ID_14052 Human_SNP_ID_411882271 A-to-I Human chr9 - 112209148 112209148 112209148 TAATTTTGTATTTTTAGTAGAGACAGGGTTTTACTACGTTGGCCAGGCCAGGCTGGTGTAGAACT TAATTTTGTATTTTTAGTAGAGACAGGGTTTTGCTACGTTGGCCAGGCCAGGCTGGTGTAGAACT T C lnc-PTBP3-1 RNACentral:URS00008B4725 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348591386 Functional Loss SNV dbSNP153 33..33 33 - - - 14053 RMVar_ID_14053 Human_SNP_ID_411882278 A-to-I Human chr9 - 112209178 112209178 112209178 GGATTACAGATGCCTGCCACCATCCCTGGCTAATTTTGTATTTTTAGTAGAGACAGGGTTTTACT GGATTACAGATGCCTGCCACCATCCCTGGCTAGTTTTGTATTTTTAGTAGAGACAGGGTTTTACT T C lnc-PTBP3-1 RNACentral:URS00008B4725 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005595351 Functional Loss SNV dbSNP153 33..33 33 - - - 14054 RMVar_ID_14054 Human_SNP_ID_411925157 A-to-I Human chr9 - 112372279 112372279 112372279 AAGCCAGGAGTTCAAGACCAGCCTGGCAACATAGTGAGACCCTGTCTCTACAAAAAAAATTCTTT AAGCCAGGAGTTCAAGACCAGCCTGGCAACATGGTGAGACCCTGTCTCTACAAAAAAAATTCTTT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017862628 Functional Loss SNV dbSNP153 33..33 33 - - - 14055 RMVar_ID_14055 Human_SNP_ID_411926915 A-to-I Human chr9 - 112379004 112379004 112379004 TTTTGTGTTTTTAGTAGAGACGGGGTTTCGCCATGTTGGGCTGGCTGGTCTCGAGCTCCTGACCT TTTTGTGTTTTTAGTAGAGACGGGGTTTCGCCGTGTTGGGCTGGCTGGTCTCGAGCTCCTGACCT T C lnc-PTBP3-4 RNACentral:URS00008B9E9D lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1187178713 Functional Loss SNV dbSNP153 33..33 33 - - - 14056 RMVar_ID_14056 Human_SNP_ID_411929170 A-to-I Human chr9 + 112387481 112387481 112387481 GGCTAAAGCGTTCTGCCCACCTCTGCCTCCCAAAGTGCTGAGATTATAGGCATGAGCCACCATGC GGCTAAAGCGTTCTGCCCACCTCTGCCTCCCATAGTGCTGAGATTATAGGCATGAGCCACCATGC A T HSDL2 Ensembl:ENSG00000119471 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935227723 Functional Loss SNV dbSNP153 33..33 33 - - - 14057 RMVar_ID_14057 Human_SNP_ID_411939106 A-to-I Human chr9 + 112429859 112429859 112429859 CCTGCTTGTAATCCCAACACTTTGGGAGGTCAAAGCAGGCCGATCGCTGGAGCCCAGGAGTTCGA CCTGCTTGTAATCCCAACACTTTGGGAGGTCAGAGCAGGCCGATCGCTGGAGCCCAGGAGTTCGA A G HSDL2 Ensembl:ENSG00000119471 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749361725 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70715,RMVar_hsa_circ_340167,RMVar_hsa_circ_368561,RMVar_hsa_circ_368602,RMVar_hsa_circ_364378,RMVar_hsa_circ_258830,RMVar_hsa_circ_258840,RMVar_hsa_circ_332372,RMVar_hsa_circ_258837,RMVar_hsa_circ_367333,RMVar_hsa_circ_355682,RMVar_hsa_circ_361814,RMVar_hsa_circ_366987,RMVar_hsa_circ_341971,RMVar_hsa_circ_258842,RMVar_hsa_circ_258841,RMVar_hsa_circ_258839,RMVar_hsa_circ_353017,RMVar_hsa_circ_366131,RMVar_hsa_circ_367530 14058 RMVar_ID_14058 Human_SNP_ID_411939143 A-to-I Human chr9 + 112429976 112429975 112429977 GTGGTGGTGTGCGCCTGTCGTCCCAACTACTCAGGGGGCTGAGGCAGGAGGATCACCTGAGCCTT GTGGTGGTGTGCGCCTGTCGTCCCAACTACTC__GGGGCTGAGGCAGGAGGATCACCTGAGCCTT CAG C HSDL2 Ensembl:ENSG00000119471 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1463747189 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_70715,RMVar_hsa_circ_340167,RMVar_hsa_circ_368561,RMVar_hsa_circ_368602,RMVar_hsa_circ_364378,RMVar_hsa_circ_258830,RMVar_hsa_circ_258840,RMVar_hsa_circ_332372,RMVar_hsa_circ_258837,RMVar_hsa_circ_367333,RMVar_hsa_circ_355682,RMVar_hsa_circ_361814,RMVar_hsa_circ_366987,RMVar_hsa_circ_341971,RMVar_hsa_circ_258842,RMVar_hsa_circ_258841,RMVar_hsa_circ_258839,RMVar_hsa_circ_353017,RMVar_hsa_circ_366131,RMVar_hsa_circ_367530 14059 RMVar_ID_14059 Human_SNP_ID_411939144 A-to-I Human chr9 + 112429976 112429976 112429976 GTGGTGGTGTGCGCCTGTCGTCCCAACTACTCAGGGGGCTGAGGCAGGAGGATCACCTGAGCCTT GTGGTGGTGTGCGCCTGTCGTCCCAACTACTCGGGGGGCTGAGGCAGGAGGATCACCTGAGCCTT A G HSDL2 Ensembl:ENSG00000119471 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs887276920 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70715,RMVar_hsa_circ_340167,RMVar_hsa_circ_368561,RMVar_hsa_circ_368602,RMVar_hsa_circ_364378,RMVar_hsa_circ_258830,RMVar_hsa_circ_258840,RMVar_hsa_circ_332372,RMVar_hsa_circ_258837,RMVar_hsa_circ_367333,RMVar_hsa_circ_355682,RMVar_hsa_circ_361814,RMVar_hsa_circ_366987,RMVar_hsa_circ_341971,RMVar_hsa_circ_258842,RMVar_hsa_circ_258841,RMVar_hsa_circ_258839,RMVar_hsa_circ_353017,RMVar_hsa_circ_366131,RMVar_hsa_circ_367530 14060 RMVar_ID_14060 Human_SNP_ID_411943956 A-to-I Human chr9 - 112451171 112451171 112451171 ATTTTTTTTGGTCTGTTTTTTGAGATGGGCTTACTCTGTCACCCAGGCTGAAGTGCAGTGGTACA ATTTTTTTTGGTCTGTTTTTTGAGATGGGCTTGCTCTGTCACCCAGGCTGAAGTGCAGTGGTACA T C C9orf147 Ensembl:ENSG00000230185 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs577079290 Functional Loss SNV dbSNP153 33..33 33 - - - 14061 RMVar_ID_14061 Human_SNP_ID_411943957 A-to-I Human chr9 - 112451171 112451171 112451171 ATTTTTTTTGGTCTGTTTTTTGAGATGGGCTTACTCTGTCACCCAGGCTGAAGTGCAGTGGTACA ATTTTTTTTGGTCTGTTTTTTGAGATGGGCTTCCTCTGTCACCCAGGCTGAAGTGCAGTGGTACA T G C9orf147 Ensembl:ENSG00000230185 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs577079290 Functional Loss SNV dbSNP153 33..33 33 - - - 14062 RMVar_ID_14062 Human_SNP_ID_411949079 A-to-I Human chr9 + 112473709 112473709 112473709 TTTAAGGATGCTGGCCAGGCGAGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGT TTTAAGGATGCTGGCCAGGCGAGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs981020882 Functional Loss SNV dbSNP153 33..33 33 - - - 14063 RMVar_ID_14063 Human_SNP_ID_411949573 A-to-I Human chr9 + 112475224 112475224 112475224 GCTTTGTTTGTTTTTTGTGTGGACAAGGTCTCACTTTGTTGCCCAGGCTGGTCTCAAACTCCTGG GCTTTGTTTGTTTTTTGTGTGGACAAGGTCTCGCTTTGTTGCCCAGGCTGGTCTCAAACTCCTGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053234125 Functional Loss SNV dbSNP153 33..33 33 - - - 14064 RMVar_ID_14064 Human_SNP_ID_411963516 A-to-I Human chr9 + 112527735 112527735 112527735 GAGGCGGGCAGATCTCTTGAGCCCAGGAGTTCAAGACCAGCCTGGACAACGTGGTGAAACCCCAT GAGGCGGGCAGATCTCTTGAGCCCAGGAGTTCGAGACCAGCCTGGACAACGTGGTGAAACCCCAT A G KIAA1958 Ensembl:ENSG00000165185 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1446472641 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104674,RMVar_hsa_circ_258851 14065 RMVar_ID_14065 Human_SNP_ID_411993089 A-to-I Human chr9 + 112652751 112652751 112652751 AAGTGATCCACCCTCCTCAGCCTTCTGAGAGTAGCTGGGACTACAGATGTACACCACCATGCCTG AAGTGATCCACCCTCCTCAGCCTTCTGAGAGTGGCTGGGACTACAGATGTACACCACCATGCCTG A G KIAA1958 Ensembl:ENSG00000165185 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1338208716 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_258854,RMVar_hsa_circ_258855 14066 RMVar_ID_14066 Human_SNP_ID_411993091 A-to-I Human chr9 + 112652761 112652761 112652761 CCCTCCTCAGCCTTCTGAGAGTAGCTGGGACTACAGATGTACACCACCATGCCTGGCTAATTTTT CCCTCCTCAGCCTTCTGAGAGTAGCTGGGACTGCAGATGTACACCACCATGCCTGGCTAATTTTT A G KIAA1958 Ensembl:ENSG00000165185 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1283921386 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_258854,RMVar_hsa_circ_258855 14067 RMVar_ID_14067 Human_SNP_ID_412001029 A-to-I Human chr9 - 112684306 112684306 112684306 TCTTGGCCTCAAGCAGTCCTCTCGATCCTCCCACCTTGGCCTCCTAAAGTGCTGAGATTACAGGT TCTTGGCCTCAAGCAGTCCTCTCGATCCTCCCGCCTTGGCCTCCTAAAGTGCTGAGATTACAGGT T C INIP Ensembl:ENSG00000148153 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs11545358 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26565129 14068 RMVar_ID_14068 Human_SNP_ID_412001048 A-to-I Human chr9 - 112684388 112684388 112684388 CCACCATGCCCAGCTAATTTTTTTTTTTTTTTAATTTTTGTAGAGACAGCATCTTGCTATGTTGC CCACCATGCCCAGCTAATTTTTTTTTTTTTTTTATTTTTGTAGAGACAGCATCTTGCTATGTTGC T A INIP Ensembl:ENSG00000148153 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1191677367 Functional Loss SNV dbSNP153 33..33 33 - - - 14069 RMVar_ID_14069 Human_SNP_ID_412001064 A-to-I Human chr9 - 112684429 112684429 112684429 CAACCCTTAGCCTCCCAAGTAGCTGAGACTACAGGCACATGCCACCATGCCCAGCTAATTTTTTT CAACCCTTAGCCTCCCAAGTAGCTGAGACTACCGGCACATGCCACCATGCCCAGCTAATTTTTTT T G INIP Ensembl:ENSG00000148153 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs895173596 Functional Loss SNV dbSNP153 33..33 33 - - - 14070 RMVar_ID_14070 Human_SNP_ID_412001238 A-to-I Human chr9 - 112685238 112685238 112685238 AAAAAATTAAAAAAAAAAAAAAAAGATTGGCTAGGTGTGCTGGTGCATGCATAGAGTCCCAGCCA AAAAAATTAAAAAAAAAAAAAAAAGATTGGCTGGGTGTGCTGGTGCATGCATAGAGTCCCAGCCA T C INIP Ensembl:ENSG00000148153 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs533131314 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26565133 14071 RMVar_ID_14071 Human_SNP_ID_412001553 A-to-I Human chr9 - 112686621 112686621 112686621 GTGGTGGCACACGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACCTG GTGGTGGCACACGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCTG T C INIP Ensembl:ENSG00000148153 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs557699893 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_709700 14072 RMVar_ID_14072 Human_SNP_ID_412001570 A-to-I Human chr9 - 112686661 112686661 112686661 AAACCCTGTCTCTACTAAAAGTATAAAAAATTAGCCATGTGTGGTGGCACACGCCTGTAATCCCA AAACCCTGTCTCTACTAAAAGTATAAAAAATTCGCCATGTGTGGTGGCACACGCCTGTAATCCCA T G INIP Ensembl:ENSG00000148153 Protein coding 3'UTR GSE38233;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,32596459 RNA-Seq:(High) rs1243300710 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_709700 14073 RMVar_ID_14073 Human_SNP_ID_412001591 A-to-I Human chr9 - 112686770 112686770 112686770 TTTTTGGCTGGGCACGGTGCCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGCAGA TTTTTGGCTGGGCACGGTGCCTCATGCCTGTAGTCCCAGCACTTTGGGAGGCCAAGGCGGGCAGA T C INIP Ensembl:ENSG00000148153 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1132086 Functional Loss SNV dbSNP153 33..33 33 - - - 14074 RMVar_ID_14074 Human_SNP_ID_412001592 A-to-I Human chr9 - 112686771 112686771 112686771 CTTTTTGGCTGGGCACGGTGCCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGCAG CTTTTTGGCTGGGCACGGTGCCTCATGCCTGTGATCCCAGCACTTTGGGAGGCCAAGGCGGGCAG T C INIP Ensembl:ENSG00000148153 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1132085 Functional Loss SNV dbSNP153 33..33 33 - - - 14075 RMVar_ID_14075 Human_SNP_ID_412004979 A-to-I Human chr9 - 112701302 112701301 112701303 AGTGGACTGCTTTTATTTTTGTTTTTTGAGACAGAGTTTTGCCTTGTTGCCCAGGCTGGAGTGCA AGTGGACTGCTTTTATTTTTGTTTTTTGAGA__GAGTTTTGCCTTGTTGCCCAGGCTGGAGTGCA CTG C INIP Ensembl:ENSG00000148153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006865340 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_365942 14076 RMVar_ID_14076 Human_SNP_ID_412004981 A-to-I Human chr9 - 112701302 112701302 112701302 AGTGGACTGCTTTTATTTTTGTTTTTTGAGACAGAGTTTTGCCTTGTTGCCCAGGCTGGAGTGCA AGTGGACTGCTTTTATTTTTGTTTTTTGAGACGGAGTTTTGCCTTGTTGCCCAGGCTGGAGTGCA T C INIP Ensembl:ENSG00000148153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1452787160 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_365942 14077 RMVar_ID_14077 Human_SNP_ID_412016746 A-to-I Human chr9 + 112752338 112752338 112752338 GAACAGGAAAATTAAAAAAGCTAATGGAGGCCAGGTGCAGTGGCTCACACCTGTAATACCAGCAC GAACAGGAAAATTAAAAAAGCTAATGGAGGCCGGGTGCAGTGGCTCACACCTGTAATACCAGCAC A G SNX30 Ensembl:ENSG00000148158 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs897982881 Functional Loss SNV dbSNP153 33..33 33 - - - 14078 RMVar_ID_14078 Human_SNP_ID_412082384 A-to-I Human chr9 - 113018238 113018238 113018238 AGTTTTGCTCTTGTTGCCTAGTCTGAAATGCAATGGTGTGATCTCGGCTCACTGCAACCTCCACC AGTTTTGCTCTTGTTGCCTAGTCTGAAATGCAGTGGTGTGATCTCGGCTCACTGCAACCTCCACC T C ZNF883 Ensembl:ENSG00000285447 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285298800 Functional Loss SNV dbSNP153 33..33 33 - - - 14079 RMVar_ID_14079 Human_SNP_ID_412131450 A-to-I Human chr9 + 113249600 113249600 113249600 GTTGGTTAGGCTGGTCTCGAACTCTTGACCTCAGGTGATCCACCCACCTTGGCCTCCCAAAGTGC GTTGGTTAGGCTGGTCTCGAACTCTTGACCTCGGGTGATCCACCCACCTTGGCCTCCCAAAGTGC A G SLC31A1 Ensembl:ENSG00000136868 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1165426897 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_258888,RMVar_hsa_circ_112707 14080 RMVar_ID_14080 Human_SNP_ID_412134444 A-to-I Human chr9 + 113262910 113262910 113262910 AGCTAGACCCAATGGCTCATGCCTGTAATCCCAACACTTTGGGAGGCCAAGGTGGGAGGATGGCT AGCTAGACCCAATGGCTCATGCCTGTAATCCCGACACTTTGGGAGGCCAAGGTGGGAGGATGGCT A G SLC31A1 Ensembl:ENSG00000136868 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1326278523 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26834159 Human_miRNA_ID_2086173,Human_miRNA_ID_2217706,Human_miRNA_ID_2845829,Human_miRNA_ID_2848854 RMVar_hsa_circ_78884,RMVar_hsa_circ_258888,RMVar_hsa_circ_112707,RMVar_hsa_circ_84092,RMVar_hsa_circ_258891,RMVar_hsa_circ_258892 14081 RMVar_ID_14081 Human_SNP_ID_412136037 A-to-I Human chr9 + 113269137 113269137 113269137 CAGTTATTCAGGGGGCCTGATGTGGTAGGATCACCTGAGCCTGGCAGGTCAAGGCTGCAGTGAGC CAGTTATTCAGGGGGCCTGATGTGGTAGGATCCCCTGAGCCTGGCAGGTCAAGGCTGCAGTGAGC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334714729 Functional Loss SNV dbSNP153 33..33 33 - - - 14082 RMVar_ID_14082 Human_SNP_ID_412138273 A-to-I Human chr9 + 113277836 113277836 113277836 CCAGCCTGGGCAAATAGTGATACCCCATCTCTACAAAAAGTAGAAAATTAGCTGGGCATGGTGAC CCAGCCTGGGCAAATAGTGATACCCCATCTCTGCAAAAAGTAGAAAATTAGCTGGGCATGGTGAC A G PRPF4 Ensembl:ENSG00000136875 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs779339452 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73066,RMVar_hsa_circ_258894 14083 RMVar_ID_14083 Human_SNP_ID_412138280 A-to-I Human chr9 + 113277879 113277879 113277879 AAAATTAGCTGGGCATGGTGACACGTGCCTGTATTCCCAGCTAATTGGGGTTCTGAGGTGGGGGT AAAATTAGCTGGGCATGGTGACACGTGCCTGTCTTCCCAGCTAATTGGGGTTCTGAGGTGGGGGT A C PRPF4 Ensembl:ENSG00000136875 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1476485759 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73066,RMVar_hsa_circ_258894 14084 RMVar_ID_14084 Human_SNP_ID_412142539 A-to-I Human chr9 + 113293706 113293706 113293706 CTGGGCTCATGCAATCCTGCCTTGGCCTCCCAAAATGCTGGGATTACAGGCATGAGTCACTGTGC CTGGGCTCATGCAATCCTGCCTTGGCCTCCCAGAATGCTGGGATTACAGGCATGAGTCACTGTGC A G PRPF4 Ensembl:ENSG00000136875 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs919882381 Functional Loss SNV dbSNP153 33..33 33 - - - 14085 RMVar_ID_14085 Human_SNP_ID_412142546 A-to-I Human chr9 + 113293725 113293725 113293725 CCTTGGCCTCCCAAAATGCTGGGATTACAGGCATGAGTCACTGTGCCTGACCTAAACATACTGTT CCTTGGCCTCCCAAAATGCTGGGATTACAGGCGTGAGTCACTGTGCCTGACCTAAACATACTGTT A G PRPF4 Ensembl:ENSG00000136875 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs949619941 Functional Loss SNV dbSNP153 33..33 33 - - - 14086 RMVar_ID_14086 Human_SNP_ID_412148047 A-to-I Human chr9 - 113315185 113315185 113315185 CTGGCTAATTTTTTGTGTGTTTGTGTGGTCTAAAACTCCTGGGCTCAAGTGATCCATCTGCCTCG CTGGCTAATTTTTTGTGTGTTTGTGTGGTCTACAACTCCTGGGCTCAAGTGATCCATCTGCCTCG T G WDR31 Ensembl:ENSG00000148225 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1388572164 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24280750,Human_RBP_ID_26565159 14087 RMVar_ID_14087 Human_SNP_ID_412151061 A-to-I Human chr9 - 113327830 113327830 113327830 CTTCTGCCTTGGCCACCCAAGTAAGTGGGATTACAGACATGTGCCACCACACCCGGCTAATTTTT CTTCTGCCTTGGCCACCCAAGTAAGTGGGATTGCAGACATGTGCCACCACACCCGGCTAATTTTT T C WDR31 Ensembl:ENSG00000148225 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs539368642 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59453 14088 RMVar_ID_14088 Human_SNP_ID_412171858 A-to-I Human chr9 - 113408778 113408778 113408778 AAAGGGCGGGAGACTGTGGCACCTTGGAAGGTACCACTTGAAATGAGACGTGCTACGTGTTTCTG AAAGGGCGGGAGACTGTGGCACCTTGGAAGGTGCCACTTGAAATGAGACGTGCTACGTGTTTCTG T C POLE3 Ensembl:ENSG00000148229 Protein coding exon GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs775258801 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_219732,Human_RBP_ID_709940,Human_RBP_ID_798288,Human_RBP_ID_1701280,Human_RBP_ID_2059671,Human_RBP_ID_5007056,Human_RBP_ID_7890335,Human_RBP_ID_9339020,Human_RBP_ID_9407209,Human_RBP_ID_16547445,Human_RBP_ID_22119867,Human_RBP_ID_23094347,Human_RBP_ID_23117259,Human_RBP_ID_24280835,Human_RBP_ID_24549715,Human_RBP_ID_26360976,Human_RBP_ID_27832609 14089 RMVar_ID_14089 Human_SNP_ID_412186119 A-to-I Human chr9 + 113467941 113467941 113467941 TAGAGATGAGGTTTCCCTATGTTGCCCAAGCTAGTCTTGAACTCAGGGACTCAAGCGATCTCCTG TAGAGATGAGGTTTCCCTATGTTGCCCAAGCTGGTCTTGAACTCAGGGACTCAAGCGATCTCCTG A G RGS3 Ensembl:ENSG00000138835 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1375945960 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109099,RMVar_hsa_circ_258908 14090 RMVar_ID_14090 Human_SNP_ID_412289982 A-to-I Human chr9 + 113899874 113899874 113899874 GTACCTACCACATTTTGTTTATTCATTTGTCTATTAATGGATATATCAGTTGCTTCCACCTTTTG GTACCTACCACATTTTGTTTATTCATTTGTCTGTTAATGGATATATCAGTTGCTTCCACCTTTTG A G ZNF618 Ensembl:ENSG00000157657 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs983055429 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21673973 14091 RMVar_ID_14091 Human_SNP_ID_412405489 A-to-I Human chr9 - 114352380 114352379 114352381 TTGGCCAGGCTAGTCTCAAACTCCTGACCTCAAGTGATCCGCCCGCCTCAGCCTCCCAAAGTGCT TTGGCCAGGCTAGTCTCAAACTCCTGACCTC__GTGATCCGCCCGCCTCAGCCTCCCAAAGTGCT CTT C AKNA Ensembl:ENSG00000106948 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1397516207 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_38976,RMVar_hsa_circ_74954 14092 RMVar_ID_14092 Human_SNP_ID_412405492 A-to-I Human chr9 - 114352395 114352395 114352395 ATGGGTTTCACCATGTTGGCCAGGCTAGTCTCAAACTCCTGACCTCAAGTGATCCGCCCGCCTCA ATGGGTTTCACCATGTTGGCCAGGCTAGTCTCGAACTCCTGACCTCAAGTGATCCGCCCGCCTCA T C AKNA Ensembl:ENSG00000106948 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1388217486 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38976,RMVar_hsa_circ_74954 14093 RMVar_ID_14093 Human_SNP_ID_412405493 A-to-I Human chr9 - 114352401 114352401 114352401 GTAGAAATGGGTTTCACCATGTTGGCCAGGCTAGTCTCAAACTCCTGACCTCAAGTGATCCGCCC GTAGAAATGGGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTCCTGACCTCAAGTGATCCGCCC T C AKNA Ensembl:ENSG00000106948 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1298880290 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38976,RMVar_hsa_circ_74954 14094 RMVar_ID_14094 Human_SNP_ID_412405504 A-to-I Human chr9 - 114352431 114352431 114352431 CACTGCGTCCAGCTAATTTTTGTATTTTTAGTAGAAATGGGTTTCACCATGTTGGCCAGGCTAGT CACTGCGTCCAGCTAATTTTTGTATTTTTAGTGGAAATGGGTTTCACCATGTTGGCCAGGCTAGT T C AKNA Ensembl:ENSG00000106948 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1241654968 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38976,RMVar_hsa_circ_74954 14095 RMVar_ID_14095 Human_SNP_ID_412405534 A-to-I Human chr9 - 114352534 114352534 114352534 GGTATGTAGTGGTACGATCTCAGCTCACTGCAACCTCCACCACTCAGGTTCAAGTGATTCTCCAG GGTATGTAGTGGTACGATCTCAGCTCACTGCAGCCTCCACCACTCAGGTTCAAGTGATTCTCCAG T C AKNA Ensembl:ENSG00000106948 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1564626441 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38976,RMVar_hsa_circ_74954 14096 RMVar_ID_14096 Human_SNP_ID_412405540 A-to-I Human chr9 - 114352553 114352553 114352553 TCACTCTGTCCCCCAGGCTGGTATGTAGTGGTACGATCTCAGCTCACTGCAACCTCCACCACTCA TCACTCTGTCCCCCAGGCTGGTATGTAGTGGTTCGATCTCAGCTCACTGCAACCTCCACCACTCA T A AKNA Ensembl:ENSG00000106948 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1187806375 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38976,RMVar_hsa_circ_74954 14097 RMVar_ID_14097 Human_SNP_ID_412419233 A-to-I Human chr9 - 114404914 114404914 114404914 CACCAGTCAACCCACGCTGCTTCACTATGTGTATAACAGCCGGGCCCCTGAGTTTGAAACCCTAG CACCAGTCAACCCACGCTGCTTCACTATGTGTGTAACAGCCGGGCCCCTGAGTTTGAAACCCTAG T C WHRN Ensembl:ENSG00000095397 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs545946248 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113886,RMVar_hsa_circ_258952 14098 RMVar_ID_14098 Human_SNP_ID_412431604 A-to-I Human chr9 - 114455304 114455304 114455304 AGGCTGAAGTGGATCACCTGAGCTTTGGAAGTAGAGGCTGCAGTGAGCCGAGATCTAGCTGCTGC AGGCTGAAGTGGATCACCTGAGCTTTGGAAGTGGAGGCTGCAGTGAGCCGAGATCTAGCTGCTGC T C WHRN Ensembl:ENSG00000095397 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs532676780 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16548285 RMVar_hsa_circ_118274,RMVar_hsa_circ_40337,RMVar_hsa_circ_258955 14099 RMVar_ID_14099 Human_SNP_ID_412431607 A-to-I Human chr9 - 114455321 114455320 114455321 AGTCCCGGCTACTTGGGAGGCTGAAGTGGATCACCTGAGCTTTGGAAGTAGAGGCTGCAGTGAGC AGTCCCGGCTACTTGGGAGGCTGAAGTGGATC_CCTGAGCTTTGGAAGTAGAGGCTGCAGTGAGC GT G WHRN Ensembl:ENSG00000095397 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs568569754 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_16548285 RMVar_hsa_circ_118274,RMVar_hsa_circ_40337,RMVar_hsa_circ_258955 14100 RMVar_ID_14100 Human_SNP_ID_412431664 A-to-I Human chr9 - 114455605 114455605 114455605 GGCTCAAGTGATCCTCTCACCTCCGCCTTCCTAGTAGCCGGGACTACAGGCATGCACCACCATAT GGCTCAAGTGATCCTCTCACCTCCGCCTTCCTCGTAGCCGGGACTACAGGCATGCACCACCATAT T G WHRN Ensembl:ENSG00000095397 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs942992103 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118274,RMVar_hsa_circ_40337,RMVar_hsa_circ_258955 14101 RMVar_ID_14101 Human_SNP_ID_412441076 A-to-I Human chr9 + 114491650 114491650 114491650 GCGCCTCGGTTAAGGGAAAGCACCAAGATGACAGGCTTTTTGCCGCCACCCGCAAGCAGAGGGAC GCGCCTCGGTTAAGGGAAAGCACCAAGATGACCGGCTTTTTGCCGCCACCCGCAAGCAGAGGGAC A C AL138895.2 Ensembl:ENSG00000271214 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991072074 Functional Loss SNV dbSNP153 33..33 33 - - - 14102 RMVar_ID_14102 Human_SNP_ID_412441077 A-to-I Human chr9 + 114491650 114491650 114491650 GCGCCTCGGTTAAGGGAAAGCACCAAGATGACAGGCTTTTTGCCGCCACCCGCAAGCAGAGGGAC GCGCCTCGGTTAAGGGAAAGCACCAAGATGACGGGCTTTTTGCCGCCACCCGCAAGCAGAGGGAC A G AL138895.2 Ensembl:ENSG00000271214 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991072074 Functional Loss SNV dbSNP153 33..33 33 - - - 14103 RMVar_ID_14103 Human_SNP_ID_412465867 A-to-I Human chr9 + 114593733 114593733 114593733 GTTGCCTTGGCTGGTCTCGAACTCCTGGCCTCAAGTGATCCTCACATCTCAACCTCCCAAAGTGC GTTGCCTTGGCTGGTCTCGAACTCCTGGCCTCGAGTGATCCTCACATCTCAACCTCCCAAAGTGC A G ATP6V1G1 Ensembl:ENSG00000136888 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs981518543 Functional Loss SNV dbSNP153 33..33 33 - - - 14104 RMVar_ID_14104 Human_SNP_ID_412465901 A-to-I Human chr9 + 114593889 114593889 114593889 GAGGTGGGAGGATTGCTTGAAGCCACAAGTTCAAAACCAGCCTGGGCAATAAACCAAGACCCTGT GAGGTGGGAGGATTGCTTGAAGCCACAAGTTCCAAACCAGCCTGGGCAATAAACCAAGACCCTGT A C ATP6V1G1 Ensembl:ENSG00000136888 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1019285260 Functional Loss SNV dbSNP153 33..33 33 - - - 14105 RMVar_ID_14105 Human_SNP_ID_412466322 A-to-I Human chr9 + 114595402 114595402 114595402 CTAAGGGCACAGTGGCTCATGCCTGTAATGCTAGCATTTTGGGAGGCCAAGGTGGGTGGATCGTT CTAAGGGCACAGTGGCTCATGCCTGTAATGCTGGCATTTTGGGAGGCCAAGGTGGGTGGATCGTT A G ATP6V1G1 Ensembl:ENSG00000136888 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1305738325 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16548469 14106 RMVar_ID_14106 Human_SNP_ID_412466331 A-to-I Human chr9 + 114595442 114595442 114595442 GGGAGGCCAAGGTGGGTGGATCGTTTGAGCCCAGGAGTTCAAGACCTGCCTGGGCAACATGGTGA GGGAGGCCAAGGTGGGTGGATCGTTTGAGCCCGGGAGTTCAAGACCTGCCTGGGCAACATGGTGA A G ATP6V1G1 Ensembl:ENSG00000136888 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs544077663 Functional Loss SNV dbSNP153 33..33 33 - - - 14107 RMVar_ID_14107 Human_SNP_ID_412466341 A-to-I Human chr9 + 114595507 114595507 114595507 AACTCTGACTCTACAAAAAAAATACAGAAATTAGCCGGGCATGGTGGTGTATACGTGTAGTTCCA AACTCTGACTCTACAAAAAAAATACAGAAATTGGCCGGGCATGGTGGTGTATACGTGTAGTTCCA A G ATP6V1G1 Ensembl:ENSG00000136888 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1269892563 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7890882,Human_RBP_ID_16548472 14108 RMVar_ID_14108 Human_SNP_ID_412466358 A-to-I Human chr9 + 114595574 114595574 114595574 TACTTGGGAGGCTCAGGTTGGAGGATGGCTTGAGCCCAGGAGGTGGAGATTGCAGTGAGCCGAGA TACTTGGGAGGCTCAGGTTGGAGGATGGCTTGCGCCCAGGAGGTGGAGATTGCAGTGAGCCGAGA A C ATP6V1G1 Ensembl:ENSG00000136888 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1162950216 Functional Loss SNV dbSNP153 33..33 33 - - - 14109 RMVar_ID_14109 Human_SNP_ID_412472149 A-to-I Human chr9 + 114617594 114617594 114617594 TATTTCTGATTTATTTTTACTTATTTAGAGACAGGGTCTTGCTCTGTTATCCTGGCTGGAGTGCA TATTTCTGATTTATTTTTACTTATTTAGAGACGGGGTCTTGCTCTGTTATCCTGGCTGGAGTGCA A G TMEM268 Ensembl:ENSG00000157693 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202402316 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18112 14110 RMVar_ID_14110 Human_SNP_ID_412472340 A-to-I Human chr9 + 114618492 114618491 114618492 ACTTGAGTACATGTTTACCTGGCCAACATGGTAAAACCCTTTCTCTACTAAAAATCAGCTGGATG ACTTGAGTACATGTTTACCTGGCCAACATGGT_AAACCCTTTCTCTACTAAAAATCAGCTGGATG TA T TMEM268 Ensembl:ENSG00000157693 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1362697272 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_18112 14111 RMVar_ID_14111 Human_SNP_ID_412472359 A-to-I Human chr9 + 114618552 114618552 114618552 GGATGTGGTGGCGGGCGCCTGTAATGCCAGCTACTAGGGAGGCTGAGGCAGGATAATCACTTGAA GGATGTGGTGGCGGGCGCCTGTAATGCCAGCTGCTAGGGAGGCTGAGGCAGGATAATCACTTGAA A G TMEM268 Ensembl:ENSG00000157693 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1308577397 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18112 14112 RMVar_ID_14112 Human_SNP_ID_412472833 A-to-I Human chr9 + 114620449 114620449 114620449 TGTATTTTTTTGTAGAGACGGGGTTTTTCACCATGTTGCCCGGGTTGATCTCAACCTCCTGGGCT TGTATTTTTTTGTAGAGACGGGGTTTTTCACCGTGTTGCCCGGGTTGATCTCAACCTCCTGGGCT A G TMEM268 Ensembl:ENSG00000157693 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285104303 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18112 14113 RMVar_ID_14113 Human_SNP_ID_412473401 A-to-I Human chr9 + 114622947 114622947 114622947 ACTGTGTCTCTACTGAAATACAAAAATTAGCCAGGCATGGTGGTGCATGCCTGTAATCCCAGCTA ACTGTGTCTCTACTGAAATACAAAAATTAGCCCGGCATGGTGGTGCATGCCTGTAATCCCAGCTA A C TMEM268 Ensembl:ENSG00000157693 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs535006976 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18112 14114 RMVar_ID_14114 Human_SNP_ID_412473402 A-to-I Human chr9 + 114622947 114622947 114622947 ACTGTGTCTCTACTGAAATACAAAAATTAGCCAGGCATGGTGGTGCATGCCTGTAATCCCAGCTA ACTGTGTCTCTACTGAAATACAAAAATTAGCCTGGCATGGTGGTGCATGCCTGTAATCCCAGCTA A T TMEM268 Ensembl:ENSG00000157693 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs535006976 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18112 14115 RMVar_ID_14115 Human_SNP_ID_412473406 A-to-I Human chr9 + 114622951 114622951 114622951 TGTCTCTACTGAAATACAAAAATTAGCCAGGCATGGTGGTGCATGCCTGTAATCCCAGCTACTTG TGTCTCTACTGAAATACAAAAATTAGCCAGGCGTGGTGGTGCATGCCTGTAATCCCAGCTACTTG A G TMEM268 Ensembl:ENSG00000157693 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs957801558 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18112 14116 RMVar_ID_14116 Human_SNP_ID_412473507 A-to-I Human chr9 + 114623277 114623277 114623277 GGTTCAAGCAATTCTGCCTCAGCCTCCCCAGTAGCTGGGATTACAGGCACGTGCCACCACGCCCG GGTTCAAGCAATTCTGCCTCAGCCTCCCCAGTGGCTGGGATTACAGGCACGTGCCACCACGCCCG A G TMEM268 Ensembl:ENSG00000157693 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1040511170 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18112 14117 RMVar_ID_14117 Human_SNP_ID_412479061 A-to-I Human chr9 + 114645999 114645998 114645999 TTTTTTTTTAAATGTAATTTTTTCAGAGAGATAAGGTCTTGCTATGTTACCCAGCCTAGTCTTGA TTTTTTTTTAAATGTAATTTTTTCAGAGAGAT_AGGTCTTGCTATGTTACCCAGCCTAGTCTTGA TA T TMEM268 Ensembl:ENSG00000157693 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs981172008 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_258965 14118 RMVar_ID_14118 Human_SNP_ID_412479062 A-to-I Human chr9 + 114645999 114645999 114645999 TTTTTTTTTAAATGTAATTTTTTCAGAGAGATAAGGTCTTGCTATGTTACCCAGCCTAGTCTTGA TTTTTTTTTAAATGTAATTTTTTCAGAGAGATGAGGTCTTGCTATGTTACCCAGCCTAGTCTTGA A G TMEM268 Ensembl:ENSG00000157693 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs868737392 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_258965 14119 RMVar_ID_14119 Human_SNP_ID_412480661 A-to-I Human chr9 + 114653094 114653094 114653094 GTTGCCCAGGCTGATCTCAAACTCCTGGCCTCAAGTGATACTCCTGCCTCTGCCTCCTGTATTTC GTTGCCCAGGCTGATCTCAAACTCCTGGCCTCGAGTGATACTCCTGCCTCTGCCTCCTGTATTTC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs182839212 Functional Loss SNV dbSNP153 33..33 33 - - - 14120 RMVar_ID_14120 Human_SNP_ID_412480662 A-to-I Human chr9 + 114653094 114653094 114653094 GTTGCCCAGGCTGATCTCAAACTCCTGGCCTCAAGTGATACTCCTGCCTCTGCCTCCTGTATTTC GTTGCCCAGGCTGATCTCAAACTCCTGGCCTCTAGTGATACTCCTGCCTCTGCCTCCTGTATTTC A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs182839212 Functional Loss SNV dbSNP153 33..33 33 - - - 14121 RMVar_ID_14121 Human_SNP_ID_412480962 A-to-I Human chr9 + 114654468 114654468 114654468 TCTTCTGGCCGGGTGTAGTGGCTCACGCCTGTAATCCCAGGACTTTGGGAGGTTGAGATGGGCGG TCTTCTGGCCGGGTGTAGTGGCTCACGCCTGTCATCCCAGGACTTTGGGAGGTTGAGATGGGCGG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1427611446 Functional Loss SNV dbSNP153 33..33 33 - - - 14122 RMVar_ID_14122 Human_SNP_ID_412578212 A-to-I Human chr9 - 115049644 115049644 115049644 GCATTTACCAGTACTGTCAGAAAAAAAAAAAGAAAAAAGAAAAAACACCTAGAAAAGAGACGCTG GCATTTACCAGTACTGTCAGAAAAAAAAAAAGGAAAAAGAAAAAACACCTAGAAAAGAGACGCTG T C TNC Ensembl:ENSG00000041982 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1413202046 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104293,RMVar_hsa_circ_94035,RMVar_hsa_circ_258966,RMVar_hsa_circ_258967,RMVar_hsa_circ_267731,RMVar_hsa_circ_30518,RMVar_hsa_circ_258971,RMVar_hsa_circ_313672,RMVar_hsa_circ_348818,RMVar_hsa_circ_119011,RMVar_hsa_circ_268112,RMVar_hsa_circ_258972,RMVar_hsa_circ_343365,RMVar_hsa_circ_42967,RMVar_hsa_circ_46881 14123 RMVar_ID_14123 Human_SNP_ID_412954010 A-to-I Human chr9 - 116598501 116598501 116598501 ATTTTGCTATTACTTTACTTTCAATGGCAAAAACCACAATTAATTTTGCACCAACCTCATATCCT ATTTTGCTATTACTTTACTTTCAATGGCAAAAGCCACAATTAATTTTGCACCAACCTCATATCCT T C ASTN2 Ensembl:ENSG00000148219 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1454047812 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17604,RMVar_hsa_circ_118279,RMVar_hsa_circ_259052,RMVar_hsa_circ_87377,RMVar_hsa_circ_259051,RMVar_hsa_circ_123989,RMVar_hsa_circ_31261,RMVar_hsa_circ_259054 14124 RMVar_ID_14124 Human_SNP_ID_412998105 A-to-I Human chr9 - 116777975 116777975 116777975 AGCTGGGTGTGGTGGCACACACCTATAGTCCCAGCTGCTCGGGAGGCTGAGGCGGGAGAATTGCT AGCTGGGTGTGGTGGCACACACCTATAGTCCCTGCTGCTCGGGAGGCTGAGGCGGGAGAATTGCT T A ASTN2 Ensembl:ENSG00000148219 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs766756720 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_259052,RMVar_hsa_circ_87377,RMVar_hsa_circ_123989,RMVar_hsa_circ_94697,RMVar_hsa_circ_259054,RMVar_hsa_circ_104961,RMVar_hsa_circ_259061,RMVar_hsa_circ_43982,RMVar_hsa_circ_259060 14125 RMVar_ID_14125 Human_SNP_ID_412998106 A-to-I Human chr9 - 116777975 116777975 116777975 AGCTGGGTGTGGTGGCACACACCTATAGTCCCAGCTGCTCGGGAGGCTGAGGCGGGAGAATTGCT AGCTGGGTGTGGTGGCACACACCTATAGTCCCGGCTGCTCGGGAGGCTGAGGCGGGAGAATTGCT T C ASTN2 Ensembl:ENSG00000148219 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs766756720 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_259052,RMVar_hsa_circ_87377,RMVar_hsa_circ_123989,RMVar_hsa_circ_94697,RMVar_hsa_circ_259054,RMVar_hsa_circ_104961,RMVar_hsa_circ_259061,RMVar_hsa_circ_43982,RMVar_hsa_circ_259060 14126 RMVar_ID_14126 Human_SNP_ID_413014940 A-to-I Human chr9 - 116842504 116842503 116842504 CAGAGCCTTTCCCACTCACTTATATGCCAGGAAGCACACCAGAGCTCTCCTGGGATGAGAAGAAC CAGAGCCTTTCCCACTCACTTATATGCCAGGA_GCACACCAGAGCTCTCCTGGGATGAGAAGAAC CT C ASTN2 Ensembl:ENSG00000148219 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs912864511 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_76144,RMVar_hsa_circ_259052,RMVar_hsa_circ_87377,RMVar_hsa_circ_123989,RMVar_hsa_circ_259054,RMVar_hsa_circ_104961,RMVar_hsa_circ_259061,RMVar_hsa_circ_43982,RMVar_hsa_circ_343397,RMVar_hsa_circ_259065,RMVar_hsa_circ_33800 14127 RMVar_ID_14127 Human_SNP_ID_413015229 A-to-I Human chr9 - 116843547 116843547 116843547 TCAAGCAATTCTCCCCCATCACCCTCCCGAGTACCTGAGATTACAGGTGCCCGCCACCACCCCTG TCAAGCAATTCTCCCCCATCACCCTCCCGAGTGCCTGAGATTACAGGTGCCCGCCACCACCCCTG T C ASTN2 Ensembl:ENSG00000148219 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs764569505 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76144,RMVar_hsa_circ_259052,RMVar_hsa_circ_87377,RMVar_hsa_circ_123989,RMVar_hsa_circ_259054,RMVar_hsa_circ_104961,RMVar_hsa_circ_259061,RMVar_hsa_circ_43982,RMVar_hsa_circ_343397,RMVar_hsa_circ_259065,RMVar_hsa_circ_33800 14128 RMVar_ID_14128 Human_SNP_ID_413322732 A-to-I Human chr9 + 118083322 118083322 118083322 CACCTCCCAGCACAGCCCGTCCACAATCTCCCAGATCTTCTAGATGTCGGAGAACATCTCATTGT CACCTCCCAGCACAGCCCGTCCACAATCTCCCGGATCTTCTAGATGTCGGAGAACATCTCATTGT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879015549 Functional Loss SNV dbSNP153 33..33 33 - - - 14129 RMVar_ID_14129 Human_SNP_ID_413322745 A-to-I Human chr9 + 118083356 118083356 118083356 ATCTTCTAGATGTCGGAGAACATCTCATTGTGACTGATGAGGTCCTGGTAGATAATCATGATGGC ATCTTCTAGATGTCGGAGAACATCTCATTGTGGCTGATGAGGTCCTGGTAGATAATCATGATGGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878970859 Functional Loss SNV dbSNP153 33..33 33 - - - 14130 RMVar_ID_14130 Human_SNP_ID_725072703 A-to-I Human chrX - 93222528 93222528 93222528 TGTGCTTTTTGTAGAAGACAGCAAAATGGAGCACCAGGTCGTCCTTGCAACATGGAAGAATATTC TGTGCTTTTTGTAGAAGACAGCAAAATGGAGCGCCAGGTCGTCCTTGCAACATGGAAGAATATTC T C AL359263.1 Ensembl:ENSG00000234130 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1263098935 Functional Loss SNV dbSNP153 33..33 33 - - - 14131 RMVar_ID_14131 Human_SNP_ID_725072889 A-to-I Human chrX - 93223552 93223552 93223552 CCCAGGTGCAGCTCACTCTGCTTACTGCCATAATGAAGCTGTTTCTCAAGAAACCACCAAAACAC CCCAGGTGCAGCTCACTCTGCTTACTGCCATAGTGAAGCTGTTTCTCAAGAAACCACCAAAACAC T C AL359263.1 Ensembl:ENSG00000234130 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1325408733 Functional Loss SNV dbSNP153 33..33 33 - - - 14132 RMVar_ID_14132 Human_SNP_ID_725072896 A-to-I Human chrX - 93223587 93223587 93223587 AGAAAGCTTCCTGGAGGGTTTTCATGATGAAAACACCCAGGTGCAGCTCACTCTGCTTACTGCCA AGAAAGCTTCCTGGAGGGTTTTCATGATGAAAGCACCCAGGTGCAGCTCACTCTGCTTACTGCCA T C AL359263.1 Ensembl:ENSG00000234130 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1157690462 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17328526 14133 RMVar_ID_14133 Human_SNP_ID_725072939 A-to-I Human chrX + 93223730 93223730 93223730 TCCAGCGAGTCTAAGTTCTCACATAGAGTGGCAATGATACTTTCATACTTGTTGGAGTATTTGCG TCCAGCGAGTCTAAGTTCTCACATAGAGTGGCGATGATACTTTCATACTTGTTGGAGTATTTGCG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879231422 Functional Loss SNV dbSNP153 33..33 33 - - - 14134 RMVar_ID_14134 Human_SNP_ID_725072942 A-to-I Human chrX + 93223753 93223753 93223753 TAGAGTGGCAATGATACTTTCATACTTGTTGGAGTATTTGCGGAAGATGTCCCTGATGACAACAA TAGAGTGGCAATGATACTTTCATACTTGTTGGGGTATTTGCGGAAGATGTCCCTGATGACAACAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878960852 Functional Loss SNV dbSNP153 33..33 33 - - - 14135 RMVar_ID_14135 Human_SNP_ID_725073049 A-to-I Human chrX - 93224277 93224277 93224277 GGCTCAGAGCATCTGTGAGCGGGTAACTCCCCAGCTATCCCATGCCAACTCAGCAGTGGTGCTTT GGCTCAGAGCATCTGTGAGCGGGTAACTCCCCGGCTATCCCATGCCAACTCAGCAGTGGTGCTTT T C AL359263.1 Ensembl:ENSG00000234130 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs905357924 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17443178,Human_RBP_ID_22413435 Human_miRNA_ID_1853728,Human_miRNA_ID_1863804,Human_miRNA_ID_1879266,Human_miRNA_ID_1904300 14136 RMVar_ID_14136 Human_SNP_ID_725073056 A-to-I Human chrX - 93224311 93224311 93224311 GCCTGTCTAATTACAACCCTAAAAATGATCGGAAGGCTCAGAGCATCTGTGAGCGGGTAACTCCC GCCTGTCTAATTACAACCCTAAAAATGATCGGGAGGCTCAGAGCATCTGTGAGCGGGTAACTCCC T C AL359263.1 Ensembl:ENSG00000234130 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1382016416 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17443178,Human_RBP_ID_22413355 Human_miRNA_ID_1895876,Human_miRNA_ID_1905128 14137 RMVar_ID_14137 Human_SNP_ID_725073062 A-to-I Human chrX - 93224320 93224320 93224320 TGCTGGACTGCCTGTCTAATTACAACCCTAAAAATGATCGGAAGGCTCAGAGCATCTGTGAGCGG TGCTGGACTGCCTGTCTAATTACAACCCTAAAGATGATCGGAAGGCTCAGAGCATCTGTGAGCGG T C AL359263.1 Ensembl:ENSG00000234130 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1405497186 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22413355 Human_miRNA_ID_1895876,Human_miRNA_ID_1905128 14138 RMVar_ID_14138 Human_SNP_ID_725073090 A-to-I Human chrX + 93224520 93224520 93224520 CACCATTGGATTTGAATCTGCTATGAGACCCCATAGAGAATCCAAAAATCCCTGATCTTCCACCA CACCATTGGATTTGAATCTGCTATGAGACCCCGTAGAGAATCCAAAAATCCCTGATCTTCCACCA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1185937565 Functional Loss SNV dbSNP153 33..33 33 - - - 14139 RMVar_ID_14139 Human_SNP_ID_725073136 A-to-I Human chrX + 93224749 93224749 93224749 AGATTAGGATCTTCACAGTCCTTCACAAAGCTATTTACAGCTATGATGGCCATGTCTGGCTGACT AGATTAGGATCTTCACAGTCCTTCACAAAGCTGTTTACAGCTATGATGGCCATGTCTGGCTGACT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1490305071 Functional Loss SNV dbSNP153 33..33 33 - - - 14140 RMVar_ID_14140 Human_SNP_ID_725522869 A-to-I Human chrX + 95500016 95500016 95500016 ATAGAGGCTAACAAGTCAACTATGAAGAATTCATACAGATGACTGCAAAATGAAGACCTATTTTC ATAGAGGCTAACAAGTCAACTATGAAGAATTCGTACAGATGACTGCAAAATGAAGACCTATTTTC A G CALM1P1 Ensembl:ENSG00000223467 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1178033448 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8277833,Human_RBP_ID_17443044 14141 RMVar_ID_14141 Human_SNP_ID_725754373 A-to-I Human chrX + 96728313 96728313 96728313 TTCACTGCAACCTCTGCCTTCCAGGTTCAAGCAATTCTCCTGCCTCAGTCTCCCAAGTAGCTGGG TTCACTGCAACCTCTGCCTTCCAGGTTCAAGCGATTCTCCTGCCTCAGTCTCCCAAGTAGCTGGG A G DIAPH2 Ensembl:ENSG00000147202 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1276610146 Functional Loss SNV dbSNP153 33..33 33 - - - 14142 RMVar_ID_14142 Human_SNP_ID_725844508 A-to-I Human chrX + 97249942 97249942 97249942 CAACATGGAGAAACCCCGTCTCTACTAAAAATACAAAATTAGCCAGGCATAGTGGTGCATGCCTG CAACATGGAGAAACCCCGTCTCTACTAAAAATGCAAAATTAGCCAGGCATAGTGGTGCATGCCTG A G DIAPH2 Ensembl:ENSG00000147202 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1164499735 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_186770 RMVar_hsa_circ_99308,RMVar_hsa_circ_82484,RMVar_hsa_circ_263248,RMVar_hsa_circ_263249,RMVar_hsa_circ_52928,RMVar_hsa_circ_102043,RMVar_hsa_circ_263253,RMVar_hsa_circ_352892,RMVar_hsa_circ_361144,RMVar_hsa_circ_54306,RMVar_hsa_circ_353730,RMVar_hsa_circ_368874 14143 RMVar_ID_14143 Human_SNP_ID_725957821 A-to-I Human chrX + 97906840 97906840 97906840 AGTTAAAGATGGGGGAGTATTTGATTTCAGAGAAATGAGATTAGATTGGTTTAGGTTACAGACTT AGTTAAAGATGGGGGAGTATTTGATTTCAGAGGAATGAGATTAGATTGGTTTAGGTTACAGACTT A G AL354685.2 Ensembl:ENSG00000237752 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1360867828 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1842356 14144 RMVar_ID_14144 Human_SNP_ID_725957824 A-to-I Human chrX + 97906869 97906869 97906869 GAGAAATGAGATTAGATTGGTTTAGGTTACAGACTTATACTAGTGTCTCTAAGACTTCACTTGGC GAGAAATGAGATTAGATTGGTTTAGGTTACAGGCTTATACTAGTGTCTCTAAGACTTCACTTGGC A G AL354685.2 Ensembl:ENSG00000237752 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1394505552 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22413420 14145 RMVar_ID_14145 Human_SNP_ID_725957828 A-to-I Human chrX + 97906890 97906890 97906890 TTAGGTTACAGACTTATACTAGTGTCTCTAAGACTTCACTTGGCCTTTCAGATCACAGAGAACTT TTAGGTTACAGACTTATACTAGTGTCTCTAAGGCTTCACTTGGCCTTTCAGATCACAGAGAACTT A G AL354685.2 Ensembl:ENSG00000237752 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1172963431 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1880155,Human_miRNA_ID_1881403 14146 RMVar_ID_14146 Human_SNP_ID_726426788 A-to-I Human chrX - 100548403 100548403 100548403 TAGTAGCTGGGATTACAGGCATGTGCCACCACACCCAGCTAATTTTGTATTTTTTTTTTTAGTAG TAGTAGCTGGGATTACAGGCATGTGCCACCACGCCCAGCTAATTTTGTATTTTTTTTTTTAGTAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1454589650 Functional Loss SNV dbSNP153 33..33 33 - - - 14147 RMVar_ID_14147 Human_SNP_ID_726503662 A-to-I Human chrX - 101008560 101008560 101008560 GGAGTACAGTGGCGTGATCTCAGCTCACTGCAACCTCTCCGCCTCCCGGTTCAAGCGATTCCCCT GGAGTACAGTGGCGTGATCTCAGCTCACTGCAGCCTCTCCGCCTCCCGGTTCAAGCGATTCCCCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1569467746 Functional Loss SNV dbSNP153 33..33 33 - - - 14148 RMVar_ID_14148 Human_SNP_ID_726503923 A-to-I Human chrX - 101010404 101010392 101010404 CTCTGGTCTGAGGCAGATTTTTTTTTTGAGATAGAGTCTCACTCTTGCCCAGGCTGGAGTGTCGT CTCTGGTCTGAGGCAGATTTTTTTTTTGAGAT____________TTGCCCAGGCTGGAGTGTCGT AGAGTGAGACTCT A TRMT2B Ensembl:ENSG00000188917 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1168544681 Functional Loss DEL dbSNP153 33..44 33 - - - Human_RBP_ID_16772376 14149 RMVar_ID_14149 Human_SNP_ID_726503924 A-to-I Human chrX - 101010402 101010402 101010402 CTGGTCTGAGGCAGATTTTTTTTTTGAGATAGAGTCTCACTCTTGCCCAGGCTGGAGTGTCGTGG CTGGTCTGAGGCAGATTTTTTTTTTGAGATAGGGTCTCACTCTTGCCCAGGCTGGAGTGTCGTGG T C TRMT2B Ensembl:ENSG00000188917 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs3207291 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16772376 14150 RMVar_ID_14150 Human_SNP_ID_726503925 A-to-I Human chrX - 101010404 101010404 101010404 CTCTGGTCTGAGGCAGATTTTTTTTTTGAGATAGAGTCTCACTCTTGCCCAGGCTGGAGTGTCGT CTCTGGTCTGAGGCAGATTTTTTTTTTGAGATGGAGTCTCACTCTTGCCCAGGCTGGAGTGTCGT T C TRMT2B Ensembl:ENSG00000188917 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs3207290 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16772376 14151 RMVar_ID_14151 Human_SNP_ID_726504467 A-to-I Human chrX - 101013676 101013676 101013676 ATGGTCTCGGCTCACTACAGCCTCCACCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTG ATGGTCTCGGCTCACTACAGCCTCCACCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTG T C TRMT2B Ensembl:ENSG00000188917 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs768241847 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112117,RMVar_hsa_circ_263269 14152 RMVar_ID_14152 Human_SNP_ID_726504470 A-to-I Human chrX - 101013683 101013683 101013683 CAGTGGCATGGTCTCGGCTCACTACAGCCTCCACCTCCCAGGTTCAAGCGATTCTCCTGCCTCAG CAGTGGCATGGTCTCGGCTCACTACAGCCTCCGCCTCCCAGGTTCAAGCGATTCTCCTGCCTCAG T C TRMT2B Ensembl:ENSG00000188917 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1363433905 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112117,RMVar_hsa_circ_263269 14153 RMVar_ID_14153 Human_SNP_ID_726508206 A-to-I Human chrX - 101035088 101035088 101035088 CCACCTTCTGTATCCCAGAGTATGCTGGGATTATAGGCATGAGCTACCGTGCCTGACCTCTGAGA CCACCTTCTGTATCCCAGAGTATGCTGGGATTGTAGGCATGAGCTACCGTGCCTGACCTCTGAGA T C TRMT2B Ensembl:ENSG00000188917 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1026524505 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63150,RMVar_hsa_circ_91737,RMVar_hsa_circ_126572,RMVar_hsa_circ_263274,RMVar_hsa_circ_263273,RMVar_hsa_circ_365649,RMVar_hsa_circ_120367,RMVar_hsa_circ_263276,RMVar_hsa_circ_263275,RMVar_hsa_circ_70732,RMVar_hsa_circ_67808,RMVar_hsa_circ_315853,RMVar_hsa_circ_334791 14154 RMVar_ID_14154 Human_SNP_ID_726508880 A-to-I Human chrX - 101038915 101038915 101038915 GAAACCCCATCTCTACTAAAAATACAAAAAATAAGCCAGGTTTGGTGGCGTGTGCTTGTAGTCCC GAAACCCCATCTCTACTAAAAATACAAAAAATGAGCCAGGTTTGGTGGCGTGTGCTTGTAGTCCC T C TRMT2B Ensembl:ENSG00000188917 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1334264350 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126572,RMVar_hsa_circ_263274,RMVar_hsa_circ_365649,RMVar_hsa_circ_120367,RMVar_hsa_circ_263276,RMVar_hsa_circ_263275,RMVar_hsa_circ_67808,RMVar_hsa_circ_315853,RMVar_hsa_circ_334791,RMVar_hsa_circ_263285,RMVar_hsa_circ_342314,RMVar_hsa_circ_273807,RMVar_hsa_circ_263284,RMVar_hsa_circ_269694,RMVar_hsa_circ_63129 14155 RMVar_ID_14155 Human_SNP_ID_726508881 A-to-I Human chrX - 101038915 101038915 101038915 GAAACCCCATCTCTACTAAAAATACAAAAAATAAGCCAGGTTTGGTGGCGTGTGCTTGTAGTCCC GAAACCCCATCTCTACTAAAAATACAAAAAATCAGCCAGGTTTGGTGGCGTGTGCTTGTAGTCCC T G TRMT2B Ensembl:ENSG00000188917 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1334264350 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126572,RMVar_hsa_circ_263274,RMVar_hsa_circ_365649,RMVar_hsa_circ_120367,RMVar_hsa_circ_263276,RMVar_hsa_circ_263275,RMVar_hsa_circ_67808,RMVar_hsa_circ_315853,RMVar_hsa_circ_334791,RMVar_hsa_circ_263285,RMVar_hsa_circ_342314,RMVar_hsa_circ_273807,RMVar_hsa_circ_263284,RMVar_hsa_circ_269694,RMVar_hsa_circ_63129 14156 RMVar_ID_14156 Human_SNP_ID_726509604 A-to-I Human chrX - 101043203 101043203 101043203 GGAATGCAATGGCGCAATCTCGGCTGACTGCAACCTCTGCCTCCCAGGTTCAAACAGTTCTCCTG GGAATGCAATGGCGCAATCTCGGCTGACTGCAGCCTCTGCCTCCCAGGTTCAAACAGTTCTCCTG T C TRMT2B Ensembl:ENSG00000188917 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs746413953 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120367,RMVar_hsa_circ_263275,RMVar_hsa_circ_266294,RMVar_hsa_circ_266193 14157 RMVar_ID_14157 Human_SNP_ID_726510610 A-to-I Human chrX - 101047932 101047932 101047932 GTGCTTATGGCTGGGCATGGTGGCTCATGCCTATAATTCCAGCACTTTGGGAGGCCGAGACAGGA GTGCTTATGGCTGGGCATGGTGGCTCATGCCTGTAATTCCAGCACTTTGGGAGGCCGAGACAGGA T C TRMT2B,TRMT2B-AS1 Ensembl:ENSG00000188917,Ensembl:ENSG00000225839 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1179955332 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120367,RMVar_hsa_circ_263275,RMVar_hsa_circ_266294,RMVar_hsa_circ_266193 14158 RMVar_ID_14158 Human_SNP_ID_726510761 A-to-I Human chrX - 101048507 101048507 101048507 TTGACACAGGCAGCGGAGGTTGCGGTGAGCCAAGAATGTGCCACTGCACTCCAGCCTGGGCGACA TTGACACAGGCAGCGGAGGTTGCGGTGAGCCAGGAATGTGCCACTGCACTCCAGCCTGGGCGACA T C TRMT2B,TRMT2B-AS1 Ensembl:ENSG00000188917,Ensembl:ENSG00000225839 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs961831636 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5107644 RMVar_hsa_circ_120367,RMVar_hsa_circ_263275,RMVar_hsa_circ_266294,RMVar_hsa_circ_266193 14159 RMVar_ID_14159 Human_SNP_ID_726510876 A-to-I Human chrX - 101049272 101049272 101049272 CCAGACTGGTCTCAAACTCTTGGCCTTAAGCAATCCTCCTGCCTTGGTCTCCCAAAGTGCTGGGA CCAGACTGGTCTCAAACTCTTGGCCTTAAGCAGTCCTCCTGCCTTGGTCTCCCAAAGTGCTGGGA T C TRMT2B,TRMT2B-AS1 Ensembl:ENSG00000188917,Ensembl:ENSG00000225839 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1032361641 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26246287 RMVar_hsa_circ_120367,RMVar_hsa_circ_263275,RMVar_hsa_circ_266294,RMVar_hsa_circ_266193 14160 RMVar_ID_14160 Human_SNP_ID_726511209 A-to-I Human chrX - 101050876 101050876 101050876 CACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGACTGGGTTTCACTCTGTTGGTCAGGCTGC CACCACGCCCAGCTAATTTTTGTATTTTTAGTGGAGACTGGGTTTCACTCTGTTGGTCAGGCTGC T C TRMT2B,TRMT2B-AS1 Ensembl:ENSG00000188917,Ensembl:ENSG00000225839 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1345418108 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16772712 RMVar_hsa_circ_120367,RMVar_hsa_circ_263275,RMVar_hsa_circ_266294,RMVar_hsa_circ_266193 14161 RMVar_ID_14161 Human_SNP_ID_726520283 A-to-I Human chrX + 101099874 101099874 101099874 CAGTGGCGCAATCACGGCTCTCTGCAGCCTCGACCCCCGGGGCTCAAGCTATTCTCCTGCCTCAC CAGTGGCGCAATCACGGCTCTCTGCAGCCTCGCCCCCCGGGGCTCAAGCTATTCTCCTGCCTCAC A C CENPI Ensembl:ENSG00000102384 Protein coding 5'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1191346214 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2223380 RMVar_hsa_circ_45146,RMVar_hsa_circ_263288,RMVar_hsa_circ_96191 14162 RMVar_ID_14162 Human_SNP_ID_726520296 A-to-I Human chrX + 101099917 101099917 101099917 TCAAGCTATTCTCCTGCCTCACCCTCCTGAGTAGATAGGACTACAGGCACGTGCGGCTATGCCTA TCAAGCTATTCTCCTGCCTCACCCTCCTGAGTCGATAGGACTACAGGCACGTGCGGCTATGCCTA A C CENPI Ensembl:ENSG00000102384 Protein coding 5'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1371357185 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45146,RMVar_hsa_circ_263288,RMVar_hsa_circ_96191 14163 RMVar_ID_14163 Human_SNP_ID_726520298 A-to-I Human chrX + 101099921 101099921 101099921 GCTATTCTCCTGCCTCACCCTCCTGAGTAGATAGGACTACAGGCACGTGCGGCTATGCCTAGCTA GCTATTCTCCTGCCTCACCCTCCTGAGTAGATGGGACTACAGGCACGTGCGGCTATGCCTAGCTA A G CENPI Ensembl:ENSG00000102384 Protein coding 5'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs754822992 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45146,RMVar_hsa_circ_263288,RMVar_hsa_circ_96191 14164 RMVar_ID_14164 Human_SNP_ID_726528429 A-to-I Human chrX + 101145672 101145672 101145672 AAGTAATTGCAGTTTTTGCCATTGAAAACAATAGCAAAAACTGCAGTTACTTTTGCACCAATTTA AAGTAATTGCAGTTTTTGCCATTGAAAACAATGGCAAAAACTGCAGTTACTTTTGCACCAATTTA A G CENPI Ensembl:ENSG00000102384 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1327974342 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_263294,RMVar_hsa_circ_19101,RMVar_hsa_circ_268940,RMVar_hsa_circ_369968,RMVar_hsa_circ_290050,RMVar_hsa_circ_263298,RMVar_hsa_circ_263299,RMVar_hsa_circ_347190,RMVar_hsa_circ_263304,RMVar_hsa_circ_263303,RMVar_hsa_circ_312017,RMVar_hsa_circ_326133,RMVar_hsa_circ_333370,RMVar_hsa_circ_292331 14165 RMVar_ID_14165 Human_SNP_ID_726531105 A-to-I Human chrX + 101160592 101160592 101160592 TTTTTGTTTTAGTAGAGACGGGGCTTCACCACATTGGCCAGGCTGGTCTCGAACTTTTGACCTTA TTTTTGTTTTAGTAGAGACGGGGCTTCACCACGTTGGCCAGGCTGGTCTCGAACTTTTGACCTTA A G CENPI Ensembl:ENSG00000102384 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1220368362 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16773893 RMVar_hsa_circ_331266,RMVar_hsa_circ_326133,RMVar_hsa_circ_263305,RMVar_hsa_circ_98931 14166 RMVar_ID_14166 Human_SNP_ID_726531703 A-to-I Human chrX + 101163780 101163780 101163780 TTTGCCTGCTGGGCGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGTGG TTTGCCTGCTGGGCGTGGTGGCTCACGCCTGTTATCCCAGCACTTTGGGAGGCCAAGGTGGGTGG A T - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1468514659 Functional Loss SNV dbSNP153 33..33 33 - - - 14167 RMVar_ID_14167 Human_SNP_ID_726531707 A-to-I Human chrX + 101163824 101163824 101163824 TTGGGAGGCCAAGGTGGGTGGATCATGAGGTCAGGAGTTCGAGATGAGGCTGGCCAATATGGTAA TTGGGAGGCCAAGGTGGGTGGATCATGAGGTCGGGAGTTCGAGATGAGGCTGGCCAATATGGTAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1298207464 Functional Loss SNV dbSNP153 33..33 33 - - - 14168 RMVar_ID_14168 Human_SNP_ID_726563504 A-to-I Human chrX - 101343069 101343069 101343069 CCAAGCCAGCGGCACGATCTCGGCTCACTGCAATCTCTGCCTCCTGGGTTCAAGCGATTCTTCTG CCAAGCCAGCGGCACGATCTCGGCTCACTGCAGTCTCTGCCTCCTGGGTTCAAGCGATTCTTCTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1303295215 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7960909 14169 RMVar_ID_14169 Human_SNP_ID_726563575 A-to-I Human chrX - 101343404 101343404 101343404 CCTAGGCAACATGCCAAGACCCCATCTCTACAAAAAATACAAAAATTAGCTGAGCATGGTGGCAC CCTAGGCAACATGCCAAGACCCCATCTCTACAGAAAATACAAAAATTAGCTGAGCATGGTGGCAC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1230255059 Functional Loss SNV dbSNP153 33..33 33 - - - 14170 RMVar_ID_14170 Human_SNP_ID_726563713 A-to-I Human chrX - 101344130 101344130 101344130 ATAAGGTTGGAGAGACCGGGTGCGGTGGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAG ATAAGGTTGGAGAGACCGGGTGCGGTGGGCTCGTGCCTGTAATCCCAGCACTTTGGGAGGCCGAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1201783575 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8034808 14171 RMVar_ID_14171 Human_SNP_ID_726563777 A-to-I Human chrX - 101344460 101344460 101344460 AGCTGGGCGTGGTGGCAGGCGCCTATAGTCCCAGCCACTTGGGAGGCTGAGGCAGGAGAATGGTG AGCTGGGCGTGGTGGCAGGCGCCTATAGTCCCGGCCACTTGGGAGGCTGAGGCAGGAGAATGGTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404032894 Functional Loss SNV dbSNP153 33..33 33 - - - 14172 RMVar_ID_14172 Human_SNP_ID_726563780 A-to-I Human chrX - 101344466 101344466 101344466 AAAAAGAGCTGGGCGTGGTGGCAGGCGCCTATAGTCCCAGCCACTTGGGAGGCTGAGGCAGGAGA AAAAAGAGCTGGGCGTGGTGGCAGGCGCCTATGGTCCCAGCCACTTGGGAGGCTGAGGCAGGAGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1412253827 Functional Loss SNV dbSNP153 33..33 33 - - - 14173 RMVar_ID_14173 Human_SNP_ID_726563781 A-to-I Human chrX - 101344468 101344468 101344468 AAAAAAAGAGCTGGGCGTGGTGGCAGGCGCCTATAGTCCCAGCCACTTGGGAGGCTGAGGCAGGA AAAAAAAGAGCTGGGCGTGGTGGCAGGCGCCTGTAGTCCCAGCCACTTGGGAGGCTGAGGCAGGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1161004320 Functional Loss SNV dbSNP153 33..33 33 - - - 14174 RMVar_ID_14174 Human_SNP_ID_726563786 A-to-I Human chrX - 101344476 101344476 101344476 ATACAAAAAAAAAAAGAGCTGGGCGTGGTGGCAGGCGCCTATAGTCCCAGCCACTTGGGAGGCTG ATACAAAAAAAAAAAGAGCTGGGCGTGGTGGCGGGCGCCTATAGTCCCAGCCACTTGGGAGGCTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs782556943 Functional Loss SNV dbSNP153 33..33 33 - - - 14175 RMVar_ID_14175 Human_SNP_ID_726563813 A-to-I Human chrX - 101344603 101344603 101344603 GGTGTTGCCGAGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGCAGA GGTGTTGCCGAGCACGGTGGCTCACGCCTGTAGTCCCAGCACTTTGGGAGGCCGAGGCAGGCAGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1250326821 Functional Loss SNV dbSNP153 33..33 33 - - - 14176 RMVar_ID_14176 Human_SNP_ID_726572599 A-to-I Human chrX + 101394166 101394166 101394166 AGCCTGTCCAACATGATGAAACCCCCATCTCTAGTAAAAATAAGAAAAAATTAGCTGGGCGTGGT AGCCTGTCCAACATGATGAAACCCCCATCTCTGGTAAAAATAAGAAAAAATTAGCTGGGCGTGGT A G RPL36A-HNRNPH2,RPL36A Ensembl:ENSG00000257529,Ensembl:ENSG00000241343 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1293942552 Functional Loss SNV dbSNP153 33..33 33 - - - 14177 RMVar_ID_14177 Human_SNP_ID_726572614 A-to-I Human chrX + 101394239 101394239 101394239 CCTGTTATCCCAGCTACTCAGGAGGCTGAAGCAGGAGAATTGTTTGAACCCAGGAGAAGGAGCTG CCTGTTATCCCAGCTACTCAGGAGGCTGAAGCTGGAGAATTGTTTGAACCCAGGAGAAGGAGCTG A T RPL36A-HNRNPH2,RPL36A Ensembl:ENSG00000257529,Ensembl:ENSG00000241343 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs782048095 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16774528 14178 RMVar_ID_14178 Human_SNP_ID_726615036 A-to-I Human chrX - 101625675 101625675 101625675 TTAGCAAGCATGTGCTGATACTCATTAGTAACAGTCATATTTGTAAGCAATCTCAGTCCAGCAAG TTAGCAAGCATGTGCTGATACTCATTAGTAACGGTCATATTTGTAAGCAATCTCAGTCCAGCAAG T C ARMCX3-AS1 RNACentral:URS00008C1358 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs782302901 Functional Loss SNV dbSNP153 33..33 33 - - - 14179 RMVar_ID_14179 Human_SNP_ID_726780935 A-to-I Human chrX + 102734549 102734549 102734549 TGAGGAAGCAGAATCAGTAGAACCTGAGAGGCAGAGGTTGCAGTGAGCCGAGATTGGGCTACTGC TGAGGAAGCAGAATCAGTAGAACCTGAGAGGCGGAGGTTGCAGTGAGCCGAGATTGGGCTACTGC A G BHLHB9,ARMCX5-GPRASP2 Ensembl:ENSG00000198908,Ensembl:ENSG00000286237 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1346839191 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16775510 14180 RMVar_ID_14180 Human_SNP_ID_726929369 A-to-I Human chrX + 103609338 103609338 103609338 AGGGCAAGCCAGCCTCCCAGGCAAAGCCAGAGAGCCAGCCGCGGGCCGCCGAAAAGCGCCCGGCT AGGGCAAGCCAGCCTCCCAGGCAAAGCCAGAGGGCCAGCCGCGGGCCGCCGAAAAGCGCCCGGCT A G TCEAL3 Ensembl:ENSG00000196507 Protein coding CDS GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs765368459 Functional Loss SNV dbSNP153 33..33 33 - - - 14181 RMVar_ID_14181 Human_SNP_ID_726929379 A-to-I Human chrX + 103609372 103609372 103609372 CCAGCCGCGGGCCGCCGAAAAGCGCCCGGCTGAAGATTATGTGCCCCGGAAAGCAAAAAGAAAAA CCAGCCGCGGGCCGCCGAAAAGCGCCCGGCTGCAGATTATGTGCCCCGGAAAGCAAAAAGAAAAA A C TCEAL3 Ensembl:ENSG00000196507 Protein coding CDS GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1260849511 Functional Loss SNV dbSNP153 33..33 33 - - - 14182 RMVar_ID_14182 Human_SNP_ID_726929380 A-to-I Human chrX + 103609372 103609372 103609372 CCAGCCGCGGGCCGCCGAAAAGCGCCCGGCTGAAGATTATGTGCCCCGGAAAGCAAAAAGAAAAA CCAGCCGCGGGCCGCCGAAAAGCGCCCGGCTGGAGATTATGTGCCCCGGAAAGCAAAAAGAAAAA A G TCEAL3 Ensembl:ENSG00000196507 Protein coding CDS GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1260849511 Functional Loss SNV dbSNP153 33..33 33 - - - 14183 RMVar_ID_14183 Human_SNP_ID_726932562 A-to-I Human chrX + 103630376 103630376 103630376 AACTGATGATAATGCACTGGAAGGCAAAACGGAGCCGTCCTTATCCTATTTAATGTGTTCGGCCT AACTGATGATAATGCACTGGAAGGCAAAACGGGGCCGTCCTTATCCTATTTAATGTGTTCGGCCT A G TCEAL1 Ensembl:ENSG00000172465 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1063678 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_724292 14184 RMVar_ID_14184 Human_SNP_ID_726935978 A-to-I Human chrX - 103651804 103651804 103651804 CACCATCAATTATAGCTGCTCAACGTCAAACGATATTAGCAGAATACAATATGTCTTGTGATGAT CACCATCAATTATAGCTGCTCAACGTCAAACGTTATTAGCAGAATACAATATGTCTTGTGATGAT T A AL049610.1 Ensembl:ENSG00000180284 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs764287811 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1910807 14185 RMVar_ID_14185 Human_SNP_ID_726940022 A-to-I Human chrX - 103676473 103676473 103676473 AAGGAATATGCGGTTAATGAAGTTGTGGCAGGAATAAAAGAATATTTCAATGTGATGTTGGGCAC AAGGAATATGCGGTTAATGAAGTTGTGGCAGGGATAAAAGAATATTTCAATGTGATGTTGGGCAC T C MORF4L2 Ensembl:ENSG00000123562 Protein coding CDS GSE56152;GSE100210 embryonic stem cells,wild type;HepG2 cell line - 25708366,29129909 RNA-Seq:(High) rs749681261 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_93644,Human_RBP_ID_220054,Human_RBP_ID_724348,Human_RBP_ID_1709533,Human_RBP_ID_2068155,Human_RBP_ID_9241710,Human_RBP_ID_9409427,Human_RBP_ID_16779768,Human_RBP_ID_18913315,Human_RBP_ID_24320049,Human_RBP_ID_27141029 RMVar_hsa_circ_89385,RMVar_hsa_circ_263380 14186 RMVar_ID_14186 Human_SNP_ID_727015632 A-to-I Human chrX - 104125124 104125124 104125124 AAGTTGTTTTTTGGCCCGGCGTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGC AAGTTGTTTTTTGGCCCGGCGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGC T C SLC25A53 Ensembl:ENSG00000269743 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049037169 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_189016 14187 RMVar_ID_14187 Human_SNP_ID_727015801 A-to-I Human chrX - 104126181 104126181 104126181 CCTCAGCCTCCCAAGTAGCTAAGACTGCAGGCATGTGCCACCATACCTGGCTAATTTTTAATTTT CCTCAGCCTCCCAAGTAGCTAAGACTGCAGGCGTGTGCCACCATACCTGGCTAATTTTTAATTTT T C SLC25A53 Ensembl:ENSG00000269743 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs782682424 Functional Loss SNV dbSNP153 33..33 33 - - - 14188 RMVar_ID_14188 Human_SNP_ID_727015839 A-to-I Human chrX - 104126424 104126424 104126424 ATCTCAAACCCCTGGCCTCAAGTGATGCTCTCACCTTAGCCTCCCAAAGTGCTGGGAATACAGGT ATCTCAAACCCCTGGCCTCAAGTGATGCTCTCGCCTTAGCCTCCCAAAGTGCTGGGAATACAGGT T C SLC25A53 Ensembl:ENSG00000269743 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1556364354 Functional Loss SNV dbSNP153 33..33 33 - - - 14189 RMVar_ID_14189 Human_SNP_ID_727015846 A-to-I Human chrX - 104126436 104126436 104126436 TTGCCCAGGCTTATCTCAAACCCCTGGCCTCAAGTGATGCTCTCACCTTAGCCTCCCAAAGTGCT TTGCCCAGGCTTATCTCAAACCCCTGGCCTCACGTGATGCTCTCACCTTAGCCTCCCAAAGTGCT T G SLC25A53 Ensembl:ENSG00000269743 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1434173005 Functional Loss SNV dbSNP153 33..33 33 - - - 14190 RMVar_ID_14190 Human_SNP_ID_727015857 A-to-I Human chrX - 104126488 104126488 104126488 CACCATACCTGACTAATGTTTTAATTTTTTTTAGAGATGGGGTCTCACTATGTTGCCCAGGCTTA CACCATACCTGACTAATGTTTTAATTTTTTTTGGAGATGGGGTCTCACTATGTTGCCCAGGCTTA T C SLC25A53 Ensembl:ENSG00000269743 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1431508839 Functional Loss SNV dbSNP153 33..33 33 - - - 14191 RMVar_ID_14191 Human_SNP_ID_727015865 A-to-I Human chrX - 104126538 104126538 104126538 GTAATCCTCCTGCCTCAGCCTCCTGAGTACCCAGGACCACAGATGTGCACCACCATACCTGACTA GTAATCCTCCTGCCTCAGCCTCCTGAGTACCCGGGACCACAGATGTGCACCACCATACCTGACTA T C SLC25A53 Ensembl:ENSG00000269743 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1323674984 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16780647,Human_RBP_ID_24320329 14192 RMVar_ID_14192 Human_SNP_ID_727015872 A-to-I Human chrX - 104126572 104126572 104126572 ATCATGTCTCACTGAAGCTTTGATGTGGACTCAAGTAATCCTCCTGCCTCAGCCTCCTGAGTACC ATCATGTCTCACTGAAGCTTTGATGTGGACTCGAGTAATCCTCCTGCCTCAGCCTCCTGAGTACC T C SLC25A53 Ensembl:ENSG00000269743 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs782226178 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16780648 14193 RMVar_ID_14193 Human_SNP_ID_635188404 A-to-I Human chr18 + 161111 161111 161111 CACCATGCCTAGCTCATTTTTGTATTTTTAGTAGAAACGAGGTTTCACCGTATTGGCCAGGCTGG CACCATGCCTAGCTCATTTTTGTATTTTTAGTGGAAACGAGGTTTCACCGTATTGGCCAGGCTGG A G USP14 Ensembl:ENSG00000101557 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1485881049 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13254798 RMVar_hsa_circ_188160,RMVar_hsa_circ_97993 14194 RMVar_ID_14194 Human_SNP_ID_635190331 A-to-I Human chr18 + 168624 168623 168625 GCCTGGCTAATTTTTGTATTTTTGGTAGAGACAGGGTTTCGCAACGTTGGCCAGGCTGGTCTCGA GCCTGGCTAATTTTTGTATTTTTGGTAGAGAC__GGTTTCGCAACGTTGGCCAGGCTGGTCTCGA CAG C USP14 Ensembl:ENSG00000101557 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1189891780 Functional Loss DEL dbSNP153 33..34 33 - - - 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_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 14195 RMVar_ID_14195 Human_SNP_ID_635190332 A-to-I Human chr18 + 168624 168624 168624 GCCTGGCTAATTTTTGTATTTTTGGTAGAGACAGGGTTTCGCAACGTTGGCCAGGCTGGTCTCGA GCCTGGCTAATTTTTGTATTTTTGGTAGAGACCGGGTTTCGCAACGTTGGCCAGGCTGGTCTCGA A C USP14 Ensembl:ENSG00000101557 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs996204888 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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 14196 RMVar_ID_14196 Human_SNP_ID_635194789 A-to-I Human chr18 + 185191 185191 185191 TTTTTATTTATTTATTTTCGAGACAGAGTCTCACTCCCTCACCCAGGCTGCAGTGCAGTGGTGCG TTTTTATTTATTTATTTTCGAGACAGAGTCTCCCTCCCTCACCCAGGCTGCAGTGCAGTGGTGCG A C USP14 Ensembl:ENSG00000101557 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs977129133 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1185700 RMVar_hsa_circ_71942,RMVar_hsa_circ_331875,RMVar_hsa_circ_348058,RMVar_hsa_circ_355027,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_188167,RMVar_hsa_circ_32236,RMVar_hsa_circ_308299,RMVar_hsa_circ_349881,RMVar_hsa_circ_275321,RMVar_hsa_circ_188168 14197 RMVar_ID_14197 Human_SNP_ID_635194799 A-to-I Human chr18 + 185229 185229 185229 TCACCCAGGCTGCAGTGCAGTGGTGCGATCTCAGCTCACTGCAGCCTCTGCCTCCCGGCTTGAGC TCACCCAGGCTGCAGTGCAGTGGTGCGATCTCGGCTCACTGCAGCCTCTGCCTCCCGGCTTGAGC A G USP14 Ensembl:ENSG00000101557 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1226315015 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71942,RMVar_hsa_circ_331875,RMVar_hsa_circ_348058,RMVar_hsa_circ_355027,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_188167,RMVar_hsa_circ_32236,RMVar_hsa_circ_308299,RMVar_hsa_circ_349881,RMVar_hsa_circ_275321,RMVar_hsa_circ_188168 14198 RMVar_ID_14198 Human_SNP_ID_635199628 A-to-I Human chr18 + 205000 205000 205000 AGGCGCAAATGATCCTCCCACCTCACCCTCCCAAGTAGCTGGGACCACAGGCGTGCGCCACCATG AGGCGCAAATGATCCTCCCACCTCACCCTCCCGAGTAGCTGGGACCACAGGCGTGCGCCACCATG A G USP14 Ensembl:ENSG00000101557 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1031054194 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11542,RMVar_hsa_circ_79565,RMVar_hsa_circ_102968,RMVar_hsa_circ_188164,RMVar_hsa_circ_188165,RMVar_hsa_circ_2524,RMVar_hsa_circ_120579,RMVar_hsa_circ_188177 14199 RMVar_ID_14199 Human_SNP_ID_635199635 A-to-I Human chr18 + 205030 205030 205030 CCAAGTAGCTGGGACCACAGGCGTGCGCCACCATGCCCAGCTATTTTTTTGTATTTTTGGTAGAG CCAAGTAGCTGGGACCACAGGCGTGCGCCACCGTGCCCAGCTATTTTTTTGTATTTTTGGTAGAG A G USP14 Ensembl:ENSG00000101557 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1480488208 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11542,RMVar_hsa_circ_79565,RMVar_hsa_circ_102968,RMVar_hsa_circ_188164,RMVar_hsa_circ_188165,RMVar_hsa_circ_2524,RMVar_hsa_circ_120579,RMVar_hsa_circ_188177 14200 RMVar_ID_14200 Human_SNP_ID_635199637 A-to-I Human chr18 + 205036 205036 205036 AGCTGGGACCACAGGCGTGCGCCACCATGCCCAGCTATTTTTTTGTATTTTTGGTAGAGACAGGG AGCTGGGACCACAGGCGTGCGCCACCATGCCCGGCTATTTTTTTGTATTTTTGGTAGAGACAGGG A G USP14 Ensembl:ENSG00000101557 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs774854795 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11542,RMVar_hsa_circ_79565,RMVar_hsa_circ_102968,RMVar_hsa_circ_188164,RMVar_hsa_circ_188165,RMVar_hsa_circ_2524,RMVar_hsa_circ_120579,RMVar_hsa_circ_188177 14201 RMVar_ID_14201 Human_SNP_ID_635199758 A-to-I Human chr18 + 205587 205587 205587 CTTTAGGCCAGGAGTTCGAGACTGTCCTGGGCAACGTAGTGAAACCCTGTCTCTACAAAATATGA CTTTAGGCCAGGAGTTCGAGACTGTCCTGGGCGACGTAGTGAAACCCTGTCTCTACAAAATATGA A G USP14 Ensembl:ENSG00000101557 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904072699 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13264781 RMVar_hsa_circ_11542,RMVar_hsa_circ_79565,RMVar_hsa_circ_102968,RMVar_hsa_circ_188164,RMVar_hsa_circ_188165,RMVar_hsa_circ_2524,RMVar_hsa_circ_120579,RMVar_hsa_circ_188177 14202 RMVar_ID_14202 Human_SNP_ID_635200506 A-to-I Human chr18 + 208887 208887 208887 CATGCCTCAGCGTCCCGAGTAGCTGGGATTACAGGCGAGTGCCACCATGCCTGGCTAATTTTTGT CATGCCTCAGCGTCCCGAGTAGCTGGGATTACGGGCGAGTGCCACCATGCCTGGCTAATTTTTGT A G USP14 Ensembl:ENSG00000101557 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1429157241 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11542,RMVar_hsa_circ_79565,RMVar_hsa_circ_102968,RMVar_hsa_circ_188164,RMVar_hsa_circ_188165,RMVar_hsa_circ_2524,RMVar_hsa_circ_120579,RMVar_hsa_circ_188177 14203 RMVar_ID_14203 Human_SNP_ID_635202133 A-to-I Human chr18 - 214526 214526 214526 TCCACTGGTTTTGGTAAACAATAAACATTTTTATAACAATTGTTGTACAGTCGGCTGGTGCTCTG TCCACTGGTTTTGGTAAACAATAAACATTTTTGTAACAATTGTTGTACAGTCGGCTGGTGCTCTG T C THOC1 Ensembl:ENSG00000079134 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs185986237 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1873803,Human_RBP_ID_2536401,Human_RBP_ID_17907735,Human_RBP_ID_18715226,Human_RBP_ID_22965831,Human_RBP_ID_26647699 RMVar_hsa_circ_118717,RMVar_hsa_circ_122788,RMVar_hsa_circ_125791,RMVar_hsa_circ_120618,RMVar_hsa_circ_188180,RMVar_hsa_circ_188182,RMVar_hsa_circ_188183,RMVar_hsa_circ_188181 14204 RMVar_ID_14204 Human_SNP_ID_635204158 A-to-I Human chr18 - 222675 222675 222675 AGTGCTTGAAAATGTCTTTCACATTCTCTATTATTTCTTTCTGCCATTAGATGTTTGCTGGACCT AGTGCTTGAAAATGTCTTTCACATTCTCTATTTTTTCTTTCTGCCATTAGATGTTTGCTGGACCT T A THOC1 Ensembl:ENSG00000079134 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs201603467 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120618,RMVar_hsa_circ_20154,RMVar_hsa_circ_188180,RMVar_hsa_circ_36888,RMVar_hsa_circ_275018,RMVar_hsa_circ_188184 14205 RMVar_ID_14205 Human_SNP_ID_635204159 A-to-I Human chr18 - 222675 222675 222675 AGTGCTTGAAAATGTCTTTCACATTCTCTATTATTTCTTTCTGCCATTAGATGTTTGCTGGACCT AGTGCTTGAAAATGTCTTTCACATTCTCTATTCTTTCTTTCTGCCATTAGATGTTTGCTGGACCT T G THOC1 Ensembl:ENSG00000079134 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs201603467 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120618,RMVar_hsa_circ_20154,RMVar_hsa_circ_188180,RMVar_hsa_circ_36888,RMVar_hsa_circ_275018,RMVar_hsa_circ_188184 14206 RMVar_ID_14206 Human_SNP_ID_635204234 A-to-I Human chr18 - 222991 222991 222991 CACCCAGAAAGCAATACAGAAGGAGCAGAGTTAGAAACGATGACTTAATGATAGTTGAGGAGGTC CACCCAGAAAGCAATACAGAAGGAGCAGAGTTGGAAACGATGACTTAATGATAGTTGAGGAGGTC T C THOC1 Ensembl:ENSG00000079134 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1216455237 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120618,RMVar_hsa_circ_20154,RMVar_hsa_circ_188180,RMVar_hsa_circ_36888,RMVar_hsa_circ_275018,RMVar_hsa_circ_188184 14207 RMVar_ID_14207 Human_SNP_ID_635204250 A-to-I Human chr18 - 223065 223064 223066 AAAATGGGCAAGTTTAATAGCAGTCTAGACATAGGTAAAGTAAGAATTAATGGGTTAATTAATGA AAAATGGGCAAGTTTAATAGCAGTCTAGACA__GGTAAAGTAAGAATTAATGGGTTAATTAATGA CTA C THOC1 Ensembl:ENSG00000079134 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1376182356 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_120618,RMVar_hsa_circ_20154,RMVar_hsa_circ_188180,RMVar_hsa_circ_36888,RMVar_hsa_circ_275018,RMVar_hsa_circ_188184 14208 RMVar_ID_14208 Human_SNP_ID_635204252 A-to-I Human chr18 - 223071 223071 223071 ACTTGCAAAATGGGCAAGTTTAATAGCAGTCTAGACATAGGTAAAGTAAGAATTAATGGGTTAAT ACTTGCAAAATGGGCAAGTTTAATAGCAGTCTGGACATAGGTAAAGTAAGAATTAATGGGTTAAT T C THOC1 Ensembl:ENSG00000079134 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1433911018 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120618,RMVar_hsa_circ_20154,RMVar_hsa_circ_188180,RMVar_hsa_circ_36888,RMVar_hsa_circ_275018,RMVar_hsa_circ_188184 14209 RMVar_ID_14209 Human_SNP_ID_635204871 A-to-I Human chr18 - 225400 225400 225400 AAGCATGCTTTCATTGCTTTGTTCCCTAGTTCAAACTATGTTTTAACTGATGAGCAATCACTTTG AAGCATGCTTTCATTGCTTTGTTCCCTAGTTCTAACTATGTTTTAACTGATGAGCAATCACTTTG T A THOC1 Ensembl:ENSG00000079134 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs758850187 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3953636,Human_RBP_ID_9346459,Human_RBP_ID_25356006,Human_RBP_ID_26334255 Human_Splice_Rec_1887450,Human_Splice_Rec_1887486,Human_Splice_Rec_1887487,Human_Splice_Rec_1887506,Human_Splice_Rec_1887534,Human_Splice_Rec_1887535,Human_Splice_Rec_1887572,Human_Splice_Rec_1887573,Human_Splice_Rec_1887620,Human_Splice_Rec_1887621,Human_Splice_Rec_1887658,Human_Splice_Rec_1887659,Human_Splice_Rec_1887676,Human_Splice_Rec_1887677,Human_Splice_Rec_1887692,Human_Splice_Rec_1887716 RMVar_hsa_circ_4910,RMVar_hsa_circ_120618,RMVar_hsa_circ_20154,RMVar_hsa_circ_188180,RMVar_hsa_circ_36888,RMVar_hsa_circ_67143,RMVar_hsa_circ_328173,RMVar_hsa_circ_19595,RMVar_hsa_circ_351458 14210 RMVar_ID_14210 Human_SNP_ID_635204975 A-to-I Human chr18 + 225892 225892 225892 CTCATAATGCACTAGGTGATTTAAAGACATCCAATAAATATTGATGGCTAGGATCTGAACACTTT CTCATAATGCACTAGGTGATTTAAAGACATCCGATAAATATTGATGGCTAGGATCTGAACACTTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1413438056 Functional Loss SNV dbSNP153 33..33 33 - - - 14211 RMVar_ID_14211 Human_SNP_ID_635312830 A-to-I Human chr18 - 657352 657352 657352 GCACAGTTCCCACGTTTTCCTGCGGTCTTGTCAACAAAACTGCTGTTTGAGATCTGTTTCCTACA GCACAGTTCCCACGTTTTCCTGCGGTCTTGTCGACAAAACTGCTGTTTGAGATCTGTTTCCTACA T C TYMSOS Ensembl:ENSG00000176912 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2853741 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5098818,Human_RBP_ID_5129923 GWAS_ID_1133,GWAS_ID_1134,GWAS_ID_1135,GWAS_ID_1136 RMVar_hsa_circ_122571,RMVar_hsa_circ_188189 14212 RMVar_ID_14212 Human_SNP_ID_635312831 A-to-I Human chr18 - 657352 657352 657352 GCACAGTTCCCACGTTTTCCTGCGGTCTTGTCAACAAAACTGCTGTTTGAGATCTGTTTCCTACA GCACAGTTCCCACGTTTTCCTGCGGTCTTGTCCACAAAACTGCTGTTTGAGATCTGTTTCCTACA T G TYMSOS Ensembl:ENSG00000176912 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2853741 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5098818,Human_RBP_ID_5129923 GWAS_ID_1133,GWAS_ID_1134,GWAS_ID_1135,GWAS_ID_1136 RMVar_hsa_circ_122571,RMVar_hsa_circ_188189 14213 RMVar_ID_14213 Human_SNP_ID_635320551 A-to-I Human chr18 - 681157 681145 681158 AGCTTCTCCGATGAAAGAACGGCATAGTGGCCAGGCATAGTGGCTCACACCTGTAACCCCAGCAC AGCTTCTCCGATGAAAGAACGGCATAGTGGC_____________TCACACCTGTAACCCCAGCAC AGCCACTATGCCTG A ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs368025747 Functional Loss DEL dbSNP153 32..44 33 - - - RMVar_hsa_circ_89404,RMVar_hsa_circ_358210,RMVar_hsa_circ_267129,RMVar_hsa_circ_188197 14214 RMVar_ID_14214 Human_SNP_ID_635320555 A-to-I Human chr18 - 681157 681157 681157 AGCTTCTCCGATGAAAGAACGGCATAGTGGCCAGGCATAGTGGCTCACACCTGTAACCCCAGCAC AGCTTCTCCGATGAAAGAACGGCATAGTGGCCGGGCATAGTGGCTCACACCTGTAACCCCAGCAC T C ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs547216585 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89404,RMVar_hsa_circ_358210,RMVar_hsa_circ_267129,RMVar_hsa_circ_188197 14215 RMVar_ID_14215 Human_SNP_ID_635321413 A-to-I Human chr18 - 684105 684105 684105 CCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCGTGAACCTGGGAGGCAGAGGTT CCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCGGGAGAATGGCGTGAACCTGGGAGGCAGAGGTT T C ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1335757828 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_135512 RMVar_hsa_circ_358210,RMVar_hsa_circ_267129,RMVar_hsa_circ_66856,RMVar_hsa_circ_284124,RMVar_hsa_circ_308584,RMVar_hsa_circ_69850,RMVar_hsa_circ_188198,RMVar_hsa_circ_188199 14216 RMVar_ID_14216 Human_SNP_ID_635321567 A-to-I Human chr18 - 684493 684493 684493 ATAGGGTCTCACTCAGTCACCCAGGCTAGAGTACAGCAGCATGATCACACCTCACTGCAGCCTTG ATAGGGTCTCACTCAGTCACCCAGGCTAGAGTTCAGCAGCATGATCACACCTCACTGCAGCCTTG T A ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1030342200 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_358210,RMVar_hsa_circ_267129,RMVar_hsa_circ_66856,RMVar_hsa_circ_284124,RMVar_hsa_circ_308584,RMVar_hsa_circ_69850,RMVar_hsa_circ_188198,RMVar_hsa_circ_188199 14217 RMVar_ID_14217 Human_SNP_ID_635321570 A-to-I Human chr18 - 684511 684511 684511 TTATTATTATTTTTTGAGATAGGGTCTCACTCAGTCACCCAGGCTAGAGTACAGCAGCATGATCA TTATTATTATTTTTTGAGATAGGGTCTCACTCGGTCACCCAGGCTAGAGTACAGCAGCATGATCA T C ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1035596588 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_358210,RMVar_hsa_circ_267129,RMVar_hsa_circ_66856,RMVar_hsa_circ_284124,RMVar_hsa_circ_308584,RMVar_hsa_circ_69850,RMVar_hsa_circ_188198,RMVar_hsa_circ_188199 14218 RMVar_ID_14218 Human_SNP_ID_635321572 A-to-I Human chr18 - 684515 684515 684515 GTTATTATTATTATTTTTTGAGATAGGGTCTCACTCAGTCACCCAGGCTAGAGTACAGCAGCATG GTTATTATTATTATTTTTTGAGATAGGGTCTCTCTCAGTCACCCAGGCTAGAGTACAGCAGCATG T A ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1568045930 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_358210,RMVar_hsa_circ_267129,RMVar_hsa_circ_66856,RMVar_hsa_circ_284124,RMVar_hsa_circ_308584,RMVar_hsa_circ_69850,RMVar_hsa_circ_188198,RMVar_hsa_circ_188199 14219 RMVar_ID_14219 Human_SNP_ID_635321739 A-to-I Human chr18 - 685067 685067 685067 TTGAGGCCAGGAGTTTGGGACCAGCCTGGGCTACATAGCAAGACTCTCTCTCTAAAAGAAAGAAG TTGAGGCCAGGAGTTTGGGACCAGCCTGGGCTGCATAGCAAGACTCTCTCTCTAAAAGAAAGAAG T C ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031474523 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_358210,RMVar_hsa_circ_267129,RMVar_hsa_circ_66856,RMVar_hsa_circ_284124,RMVar_hsa_circ_308584,RMVar_hsa_circ_69850,RMVar_hsa_circ_188198,RMVar_hsa_circ_188199 14220 RMVar_ID_14220 Human_SNP_ID_635321755 A-to-I Human chr18 - 685139 685139 685139 AAAAAAGTGTTAGCATTATATGGCTCATGCCTATAATCCTAACACTTTGGGAGGCTGAAGCAGGT AAAAAAGTGTTAGCATTATATGGCTCATGCCTGTAATCCTAACACTTTGGGAGGCTGAAGCAGGT T C ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1451731366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25372808 RMVar_hsa_circ_358210,RMVar_hsa_circ_267129,RMVar_hsa_circ_66856,RMVar_hsa_circ_284124,RMVar_hsa_circ_308584,RMVar_hsa_circ_69850,RMVar_hsa_circ_188198,RMVar_hsa_circ_188199 14221 RMVar_ID_14221 Human_SNP_ID_635321784 A-to-I Human chr18 - 685223 685223 685223 AGGTGAGTGGATTGCCGGAGCTCAGGAGTACAAGATCAGCCTGGCAACATGGAAAAACCCCATCT AGGTGAGTGGATTGCCGGAGCTCAGGAGTACAGGATCAGCCTGGCAACATGGAAAAACCCCATCT T C ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1366853732 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13333721 RMVar_hsa_circ_358210,RMVar_hsa_circ_267129,RMVar_hsa_circ_66856,RMVar_hsa_circ_284124,RMVar_hsa_circ_308584,RMVar_hsa_circ_69850,RMVar_hsa_circ_188198,RMVar_hsa_circ_188199 14222 RMVar_ID_14222 Human_SNP_ID_635323760 A-to-I Human chr18 - 691414 691414 691414 ATAAGCCAGGGAGACTGAGGCTGCAGTGAGCTATGATGGCATCACTGCACTCCAGCCTGGGCAAC ATAAGCCAGGGAGACTGAGGCTGCAGTGAGCTGTGATGGCATCACTGCACTCCAGCCTGGGCAAC T C ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1278525252 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25372868 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 14223 RMVar_ID_14223 Human_SNP_ID_635323779 A-to-I Human chr18 - 691470 691470 691470 ATAGTGGCACATACCTGGAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGGATCACATAAGCCAG ATAGTGGCACATACCTGGAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGGATCACATAAGCCAG T C ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1249778069 Functional Loss SNV dbSNP153 33..33 33 - - - 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 14224 RMVar_ID_14224 Human_SNP_ID_635323780 A-to-I Human chr18 - 691470 691470 691470 ATAGTGGCACATACCTGGAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGGATCACATAAGCCAG ATAGTGGCACATACCTGGAGTCCCAGCTACTCCGGAGGCTGAGGCAGGAGGATCACATAAGCCAG T G ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1249778069 Functional Loss SNV dbSNP153 33..33 33 - - - 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 14225 RMVar_ID_14225 Human_SNP_ID_635323786 A-to-I Human chr18 - 691484 691484 691484 TAAATTAGCCGGGCATAGTGGCACATACCTGGAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGG TAAATTAGCCGGGCATAGTGGCACATACCTGGTGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGG T A ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs529534454 Functional Loss SNV dbSNP153 33..33 33 - - - 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 14226 RMVar_ID_14226 Human_SNP_ID_635323797 A-to-I Human chr18 - 691521 691517 691522 TCAACATAGTGAGACCCCATCTCTACAAAAATAAAAATAAATTAGCCGGGCATAGTGGCACATAC TCAACATAGTGAGACCCCATCTCTACAAAAA_____ATAAATTAGCCGGGCATAGTGGCACATAC TTTTTA T ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1302858103 Functional Loss DEL dbSNP153 32..36 33 - - - Human_RBP_ID_13333836,Human_RBP_ID_25372870 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 14227 RMVar_ID_14227 Human_SNP_ID_635323798 A-to-I Human chr18 - 691521 691521 691521 TCAACATAGTGAGACCCCATCTCTACAAAAATAAAAATAAATTAGCCGGGCATAGTGGCACATAC TCAACATAGTGAGACCCCATCTCTACAAAAATTAAAATAAATTAGCCGGGCATAGTGGCACATAC T A ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917189045 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13333836,Human_RBP_ID_25372870 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 14228 RMVar_ID_14228 Human_SNP_ID_635323805 A-to-I Human chr18 - 691546 691546 691546 AGCCAGGAGCTCAAGATCAACCTGGTCAACATAGTGAGACCCCATCTCTACAAAAATAAAAATAA AGCCAGGAGCTCAAGATCAACCTGGTCAACATGGTGAGACCCCATCTCTACAAAAATAAAAATAA T C ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs1161475875 Functional Loss SNV dbSNP153 33..33 33 - - - 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 14229 RMVar_ID_14229 Human_SNP_ID_635323813 A-to-I Human chr18 - 691574 691574 691574 GGGAGGCCAAGGAGGGAGGATTGCTTGAAGCCAGGAGCTCAAGATCAACCTGGTCAACATAGTGA GGGAGGCCAAGGAGGGAGGATTGCTTGAAGCCTGGAGCTCAAGATCAACCTGGTCAACATAGTGA T A ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1463313935 Functional Loss SNV dbSNP153 33..33 33 - - - 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 14230 RMVar_ID_14230 Human_SNP_ID_635323817 A-to-I Human chr18 - 691590 691590 691590 GTCATCCCAGCACTTTGGGAGGCCAAGGAGGGAGGATTGCTTGAAGCCAGGAGCTCAAGATCAAC GTCATCCCAGCACTTTGGGAGGCCAAGGAGGGGGGATTGCTTGAAGCCAGGAGCTCAAGATCAAC T C ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs930452961 Functional Loss SNV dbSNP153 33..33 33 - - - 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 14231 RMVar_ID_14231 Human_SNP_ID_635324043 A-to-I Human chr18 - 692341 692341 692341 CAGCCTCCCAAAGTGCTGGGATTACAGATGTGAGCCACCGAACCTGGCCCAGAACTCTTAGAAGT CAGCCTCCCAAAGTGCTGGGATTACAGATGTGGGCCACCGAACCTGGCCCAGAACTCTTAGAAGT T C ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170544722 Functional Loss SNV dbSNP153 33..33 33 - - - 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 14232 RMVar_ID_14232 Human_SNP_ID_635324095 A-to-I Human chr18 - 692561 692561 692561 CGGAGTTTTCTTCTTGTTGCCCAGGCTACAGTACAGTGGCATGATCTCAGCTCACTGCAACTGAT CGGAGTTTTCTTCTTGTTGCCCAGGCTACAGTGCAGTGGCATGATCTCAGCTCACTGCAACTGAT T C ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1419234913 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4491591,Human_RBP_ID_13333868,Human_RBP_ID_22965221,Human_RBP_ID_26980472 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 14233 RMVar_ID_14233 Human_SNP_ID_635325349 A-to-I Human chr18 - 696696 696694 696696 ACTGATGATCTAAATGACTCAAGACTGAATTTAGCTGAATAAAATGTTCTACTAAGGAGATGAGG ACTGATGATCTAAATGACTCAAGACTGAATTT__CTGAATAAAATGTTCTACTAAGGAGATGAGG GCT G ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1201144479 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_17567317,Human_RBP_ID_22476158 RMVar_hsa_circ_64412,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_357752,RMVar_hsa_circ_54974,RMVar_hsa_circ_327287,RMVar_hsa_circ_59154,RMVar_hsa_circ_104521,RMVar_hsa_circ_188203,RMVar_hsa_circ_326575 14234 RMVar_ID_14234 Human_SNP_ID_635325613 A-to-I Human chr18 - 697579 697579 697579 GCCCTGCTAATTTTTGTATTTTCAGTAGAGACAGGGTTTTGCCATTTTGGCCAGACTGGTCTGGA GCCCTGCTAATTTTTGTATTTTCAGTAGAGACGGGGTTTTGCCATTTTGGCCAGACTGGTCTGGA T C ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1400003614 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_358210,RMVar_hsa_circ_267129,RMVar_hsa_circ_284124,RMVar_hsa_circ_188199,RMVar_hsa_circ_357752,RMVar_hsa_circ_327287,RMVar_hsa_circ_59154,RMVar_hsa_circ_104521,RMVar_hsa_circ_188203,RMVar_hsa_circ_326575,RMVar_hsa_circ_84546,RMVar_hsa_circ_287133,RMVar_hsa_circ_188207,RMVar_hsa_circ_188208 14235 RMVar_ID_14235 Human_SNP_ID_635325964 A-to-I Human chr18 - 699012 699012 699012 AAGACCTTGTCACTACAAAAAATTTAAAAATTAGCTGGTGTGGTGTTGCGTGTAGGTCCTAGCTA AAGACCTTGTCACTACAAAAAATTTAAAAATTGGCTGGTGTGGTGTTGCGTGTAGGTCCTAGCTA T C ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1228891898 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17567410 RMVar_hsa_circ_358210,RMVar_hsa_circ_267129,RMVar_hsa_circ_284124,RMVar_hsa_circ_188199,RMVar_hsa_circ_357752,RMVar_hsa_circ_327287,RMVar_hsa_circ_59154,RMVar_hsa_circ_104521,RMVar_hsa_circ_188203,RMVar_hsa_circ_326575,RMVar_hsa_circ_84546,RMVar_hsa_circ_287133,RMVar_hsa_circ_188207,RMVar_hsa_circ_188208 14236 RMVar_ID_14236 Human_SNP_ID_635325990 A-to-I Human chr18 - 699119 699119 699119 ATGGTGGCTCACACCTGTAATCCCAACACTTCAGGAGGCCGAGGTGGGAGGATTGCTTGAGCCCA ATGGTGGCTCACACCTGTAATCCCAACACTTCCGGAGGCCGAGGTGGGAGGATTGCTTGAGCCCA T G ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388101665 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13334466,Human_RBP_ID_22476166 RMVar_hsa_circ_358210,RMVar_hsa_circ_267129,RMVar_hsa_circ_284124,RMVar_hsa_circ_188199,RMVar_hsa_circ_357752,RMVar_hsa_circ_327287,RMVar_hsa_circ_59154,RMVar_hsa_circ_104521,RMVar_hsa_circ_188203,RMVar_hsa_circ_326575,RMVar_hsa_circ_84546,RMVar_hsa_circ_287133,RMVar_hsa_circ_188207,RMVar_hsa_circ_188208 14237 RMVar_ID_14237 Human_SNP_ID_635326186 A-to-I Human chr18 - 699829 699829 699829 GCAATCCACCGGCCTTGGCCTCCCAAAGTGCTAGGATTACAGACGTGAGCCACCGCGCCCAGCCT GCAATCCACCGGCCTTGGCCTCCCAAAGTGCTGGGATTACAGACGTGAGCCACCGCGCCCAGCCT T C ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs548127953 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13334543 RMVar_hsa_circ_358210,RMVar_hsa_circ_267129,RMVar_hsa_circ_284124,RMVar_hsa_circ_188199,RMVar_hsa_circ_357752,RMVar_hsa_circ_327287,RMVar_hsa_circ_59154,RMVar_hsa_circ_104521,RMVar_hsa_circ_188203,RMVar_hsa_circ_326575,RMVar_hsa_circ_84546,RMVar_hsa_circ_287133,RMVar_hsa_circ_188207,RMVar_hsa_circ_188208 14238 RMVar_ID_14238 Human_SNP_ID_635327391 A-to-I Human chr18 - 704182 704182 704182 TGATCTGCCCACCTTGGCCTCTCAAAGTGCTAAGATTATAGGCATGAACCACCACTCTGAGCCAG TGATCTGCCCACCTTGGCCTCTCAAAGTGCTACGATTATAGGCATGAACCACCACTCTGAGCCAG T G ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1288712650 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_358210,RMVar_hsa_circ_267129,RMVar_hsa_circ_284124,RMVar_hsa_circ_188199,RMVar_hsa_circ_357752,RMVar_hsa_circ_327287,RMVar_hsa_circ_59154,RMVar_hsa_circ_104521,RMVar_hsa_circ_188203,RMVar_hsa_circ_326575,RMVar_hsa_circ_84546,RMVar_hsa_circ_287133,RMVar_hsa_circ_188207,RMVar_hsa_circ_188208 14239 RMVar_ID_14239 Human_SNP_ID_635327426 A-to-I Human chr18 - 704307 704307 704307 CTTATGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCACACACCACCACGCCCGGCTAGTTTTT CTTATGCCTCAGCCTCCCGAGTAGCTGGGATTGCAGGCACACACCACCACGCCCGGCTAGTTTTT T C ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs928128356 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_358210,RMVar_hsa_circ_267129,RMVar_hsa_circ_284124,RMVar_hsa_circ_188199,RMVar_hsa_circ_357752,RMVar_hsa_circ_327287,RMVar_hsa_circ_59154,RMVar_hsa_circ_104521,RMVar_hsa_circ_188203,RMVar_hsa_circ_326575,RMVar_hsa_circ_84546,RMVar_hsa_circ_287133,RMVar_hsa_circ_188207,RMVar_hsa_circ_188208 14240 RMVar_ID_14240 Human_SNP_ID_635327600 A-to-I Human chr18 - 704752 704752 704752 AAAATACAAAAATTACCTGGCCGTGGTGATGCATGGCTGTAATCTCAGCTACTCAGGAGGCTGAA AAAATACAAAAATTACCTGGCCGTGGTGATGCGTGGCTGTAATCTCAGCTACTCAGGAGGCTGAA T C ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404181987 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_358210,RMVar_hsa_circ_267129,RMVar_hsa_circ_284124,RMVar_hsa_circ_188199,RMVar_hsa_circ_357752,RMVar_hsa_circ_327287,RMVar_hsa_circ_59154,RMVar_hsa_circ_104521,RMVar_hsa_circ_188203,RMVar_hsa_circ_326575,RMVar_hsa_circ_84546,RMVar_hsa_circ_287133,RMVar_hsa_circ_188207,RMVar_hsa_circ_188208 14241 RMVar_ID_14241 Human_SNP_ID_635328410 A-to-I Human chr18 - 707297 707280 707298 GCCCCTTCCGGGCATGATGGCTCATGCCTGTAATCCCAGCACTTTAAGAGGCCCAAGCGGGTGGA GCCCCTTCCGGGCATGATGGCTCATGCCTGT__________________GGCCCAAGCGGGTGGA CTCTTAAAGTGCTGGGATT C ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941263100 Functional Loss DEL dbSNP153 32..49 33 - - - RMVar_hsa_circ_267129,RMVar_hsa_circ_104521,RMVar_hsa_circ_188203,RMVar_hsa_circ_84546,RMVar_hsa_circ_188208 14242 RMVar_ID_14242 Human_SNP_ID_635328410 A-to-I Human chr18 - 707298 707280 707298 AGCCCCTTCCGGGCATGATGGCTCATGCCTGTAATCCCAGCACTTTAAGAGGCCCAAGCGGGTGG AGCCCCTTCCGGGCATGATGGCTCATGCCTGT__________________GGCCCAAGCGGGTGG CTCTTAAAGTGCTGGGATT C ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941263100 Functional Loss DEL dbSNP153 33..50 33 - - - RMVar_hsa_circ_267129,RMVar_hsa_circ_104521,RMVar_hsa_circ_188203,RMVar_hsa_circ_84546,RMVar_hsa_circ_188208 14243 RMVar_ID_14243 Human_SNP_ID_635328609 A-to-I Human chr18 - 708049 708049 708049 CAAGACCAGCCTGGCCAACATGGCAAAATCCCATCTTTACTAAAAAAAAAAAAAAAAAGCTGGTC CAAGACCAGCCTGGCCAACATGGCAAAATCCCGTCTTTACTAAAAAAAAAAAAAAAAAGCTGGTC T C ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs374498712 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267129,RMVar_hsa_circ_104521,RMVar_hsa_circ_188203,RMVar_hsa_circ_84546,RMVar_hsa_circ_188208 14244 RMVar_ID_14244 Human_SNP_ID_635328610 A-to-I Human chr18 - 708062 708062 708062 GAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGGCAAAATCCCATCTTTACTAAAAAAAAAAA GAGGTCAGGAGTTCAAGACCAGCCTGGCCAACGTGGCAAAATCCCATCTTTACTAAAAAAAAAAA T C ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs905206339 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267129,RMVar_hsa_circ_104521,RMVar_hsa_circ_188203,RMVar_hsa_circ_84546,RMVar_hsa_circ_188208 14245 RMVar_ID_14245 Human_SNP_ID_635328622 A-to-I Human chr18 - 708140 708140 708140 TAATTTACTTGTGGCCGGGCGTGGTGGCTCACACCTGTAATCCTAGCACTTTGGGAGGCCGAGGC TAATTTACTTGTGGCCGGGCGTGGTGGCTCACGCCTGTAATCCTAGCACTTTGGGAGGCCGAGGC T C ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1015465170 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20340148 RMVar_hsa_circ_267129,RMVar_hsa_circ_104521,RMVar_hsa_circ_188203,RMVar_hsa_circ_84546,RMVar_hsa_circ_188208 14246 RMVar_ID_14246 Human_SNP_ID_635328712 A-to-I Human chr18 - 708427 708427 708427 GGCTCAAACAATCCTCCTGTCTTGGCCTCCCAAAGTGTTGGGATTACAGGTATGAGCCAGCATGC GGCTCAAACAATCCTCCTGTCTTGGCCTCCCAGAGTGTTGGGATTACAGGTATGAGCCAGCATGC T C ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs573574508 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13335408,Human_RBP_ID_17567320 RMVar_hsa_circ_267129,RMVar_hsa_circ_104521,RMVar_hsa_circ_188203,RMVar_hsa_circ_84546,RMVar_hsa_circ_188208 14247 RMVar_ID_14247 Human_SNP_ID_635328713 A-to-I Human chr18 - 708428 708428 708428 GGGCTCAAACAATCCTCCTGTCTTGGCCTCCCAAAGTGTTGGGATTACAGGTATGAGCCAGCATG GGGCTCAAACAATCCTCCTGTCTTGGCCTCCCCAAGTGTTGGGATTACAGGTATGAGCCAGCATG T G ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs540817482 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13335408,Human_RBP_ID_17567320 RMVar_hsa_circ_267129,RMVar_hsa_circ_104521,RMVar_hsa_circ_188203,RMVar_hsa_circ_84546,RMVar_hsa_circ_188208 14248 RMVar_ID_14248 Human_SNP_ID_635329059 A-to-I Human chr18 - 709687 709687 709687 ATCTCACTGCAACCTCTGCCTCCCATATGCAAATGATTCTCGTACCTCAGCCTCTGGAGTAGCTG ATCTCACTGCAACCTCTGCCTCCCATATGCAAGTGATTCTCGTACCTCAGCCTCTGGAGTAGCTG T C ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1199816966 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267129,RMVar_hsa_circ_104521,RMVar_hsa_circ_188203,RMVar_hsa_circ_84546,RMVar_hsa_circ_188208 14249 RMVar_ID_14249 Human_SNP_ID_635329060 A-to-I Human chr18 - 709688 709688 709688 CATCTCACTGCAACCTCTGCCTCCCATATGCAAATGATTCTCGTACCTCAGCCTCTGGAGTAGCT CATCTCACTGCAACCTCTGCCTCCCATATGCAGATGATTCTCGTACCTCAGCCTCTGGAGTAGCT T C ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1235155867 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267129,RMVar_hsa_circ_104521,RMVar_hsa_circ_188203,RMVar_hsa_circ_84546,RMVar_hsa_circ_188208 14250 RMVar_ID_14250 Human_SNP_ID_635329065 A-to-I Human chr18 - 709724 709724 709724 GCTTGTTGCCCAGCCTGGAGTGCAGTGGTGCAATCTCATCTCACTGCAACCTCTGCCTCCCATAT GCTTGTTGCCCAGCCTGGAGTGCAGTGGTGCAGTCTCATCTCACTGCAACCTCTGCCTCCCATAT T C ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1446010397 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2547291,Human_RBP_ID_13354250,Human_RBP_ID_20340203 RMVar_hsa_circ_267129,RMVar_hsa_circ_104521,RMVar_hsa_circ_188203,RMVar_hsa_circ_84546,RMVar_hsa_circ_188208 14251 RMVar_ID_14251 Human_SNP_ID_635329192 A-to-I Human chr18 - 710174 710174 710174 AGTCCAGGAGGTCGAGGCTGCAGTGAGCTGTAATTGTGTCACTGCACTCCAGCCTGGGTGAGAGA AGTCCAGGAGGTCGAGGCTGCAGTGAGCTGTAGTTGTGTCACTGCACTCCAGCCTGGGTGAGAGA T C ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1057130947 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1093020,Human_RBP_ID_2547640,Human_RBP_ID_13335479 RMVar_hsa_circ_267129,RMVar_hsa_circ_104521,RMVar_hsa_circ_188203,RMVar_hsa_circ_84546,RMVar_hsa_circ_188208 14252 RMVar_ID_14252 Human_SNP_ID_635329205 A-to-I Human chr18 - 710241 710241 710241 AGCTGGGCGTAGTTGCATGCACCTGTGGTCCCAGCCACTCAGGAGGCTGAGGTGGGAGGATCTCT AGCTGGGCGTAGTTGCATGCACCTGTGGTCCCTGCCACTCAGGAGGCTGAGGTGGGAGGATCTCT T A ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs898976578 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267129,RMVar_hsa_circ_104521,RMVar_hsa_circ_188203,RMVar_hsa_circ_84546,RMVar_hsa_circ_188208 14253 RMVar_ID_14253 Human_SNP_ID_635329226 A-to-I Human chr18 - 710289 710289 710289 CCTGAGCAACATAGTGAGACCTCGTCTCAACAAAAAAATACAAAAATTAGCTGGGCGTAGTTGCA CCTGAGCAACATAGTGAGACCTCGTCTCAACAGAAAAATACAAAAATTAGCTGGGCGTAGTTGCA T C ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1051494826 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6703672,Human_RBP_ID_25379627 RMVar_hsa_circ_267129,RMVar_hsa_circ_104521,RMVar_hsa_circ_188203,RMVar_hsa_circ_84546,RMVar_hsa_circ_188208 14254 RMVar_ID_14254 Human_SNP_ID_635329227 A-to-I Human chr18 - 710292 710292 710292 CAGCCTGAGCAACATAGTGAGACCTCGTCTCAACAAAAAAATACAAAAATTAGCTGGGCGTAGTT CAGCCTGAGCAACATAGTGAGACCTCGTCTCACCAAAAAAATACAAAAATTAGCTGGGCGTAGTT T G ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs538259484 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6703672,Human_RBP_ID_25379627 RMVar_hsa_circ_267129,RMVar_hsa_circ_104521,RMVar_hsa_circ_188203,RMVar_hsa_circ_84546,RMVar_hsa_circ_188208 14255 RMVar_ID_14255 Human_SNP_ID_635329232 A-to-I Human chr18 - 710313 710313 710313 TTGAGCCCAGGAGTTCGAGACCAGCCTGAGCAACATAGTGAGACCTCGTCTCAACAAAAAAATAC TTGAGCCCAGGAGTTCGAGACCAGCCTGAGCAGCATAGTGAGACCTCGTCTCAACAAAAAAATAC T C ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs964671738 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20340217,Human_RBP_ID_25373077 RMVar_hsa_circ_267129,RMVar_hsa_circ_104521,RMVar_hsa_circ_188203,RMVar_hsa_circ_84546,RMVar_hsa_circ_188208 14256 RMVar_ID_14256 Human_SNP_ID_635329420 A-to-I Human chr18 - 711070 711070 711070 GACCTCCCTGACTCAACCAATCCTCCCACCTCAGCCTCCCAAGTAGCTGGGACTACAGGTGTGCA GACCTCCCTGACTCAACCAATCCTCCCACCTCCGCCTCCCAAGTAGCTGGGACTACAGGTGTGCA T G ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1338145600 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267129,RMVar_hsa_circ_104521,RMVar_hsa_circ_188203,RMVar_hsa_circ_84546,RMVar_hsa_circ_188208 14257 RMVar_ID_14257 Human_SNP_ID_635329422 A-to-I Human chr18 - 711075 711075 711075 GCCTTGACCTCCCTGACTCAACCAATCCTCCCACCTCAGCCTCCCAAGTAGCTGGGACTACAGGT GCCTTGACCTCCCTGACTCAACCAATCCTCCCTCCTCAGCCTCCCAAGTAGCTGGGACTACAGGT T A ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1463921058 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267129,RMVar_hsa_circ_104521,RMVar_hsa_circ_188203,RMVar_hsa_circ_84546,RMVar_hsa_circ_188208 14258 RMVar_ID_14258 Human_SNP_ID_635329426 A-to-I Human chr18 - 711083 711083 711083 TCACAGCAGCCTTGACCTCCCTGACTCAACCAATCCTCCCACCTCAGCCTCCCAAGTAGCTGGGA TCACAGCAGCCTTGACCTCCCTGACTCAACCAGTCCTCCCACCTCAGCCTCCCAAGTAGCTGGGA T C ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs571981716 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267129,RMVar_hsa_circ_104521,RMVar_hsa_circ_188203,RMVar_hsa_circ_84546,RMVar_hsa_circ_188208 14259 RMVar_ID_14259 Human_SNP_ID_635329427 A-to-I Human chr18 - 711084 711084 711084 CTCACAGCAGCCTTGACCTCCCTGACTCAACCAATCCTCCCACCTCAGCCTCCCAAGTAGCTGGG CTCACAGCAGCCTTGACCTCCCTGACTCAACCCATCCTCCCACCTCAGCCTCCCAAGTAGCTGGG T G ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1023536261 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267129,RMVar_hsa_circ_104521,RMVar_hsa_circ_188203,RMVar_hsa_circ_84546,RMVar_hsa_circ_188208 14260 RMVar_ID_14260 Human_SNP_ID_635329437 A-to-I Human chr18 - 711123 711123 711123 ATCTGTTGCCCAAGCTGGAGTGCAGTGGTACTATCATGGCTCACAGCAGCCTTGACCTCCCTGAC ATCTGTTGCCCAAGCTGGAGTGCAGTGGTACTGTCATGGCTCACAGCAGCCTTGACCTCCCTGAC T C ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs539383449 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2547946,Human_RBP_ID_13335505,Human_RBP_ID_17567321 RMVar_hsa_circ_267129,RMVar_hsa_circ_104521,RMVar_hsa_circ_188203,RMVar_hsa_circ_84546,RMVar_hsa_circ_188208 14261 RMVar_ID_14261 Human_SNP_ID_635329443 A-to-I Human chr18 - 711143 711143 711143 ATTTTGAGGCAGGGTCTCTTATCTGTTGCCCAAGCTGGAGTGCAGTGGTACTATCATGGCTCACA ATTTTGAGGCAGGGTCTCTTATCTGTTGCCCAGGCTGGAGTGCAGTGGTACTATCATGGCTCACA T C ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1229507771 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13335508,Human_RBP_ID_17567321,Human_RBP_ID_24483119 RMVar_hsa_circ_267129,RMVar_hsa_circ_104521,RMVar_hsa_circ_188203,RMVar_hsa_circ_84546,RMVar_hsa_circ_188208 14262 RMVar_ID_14262 Human_SNP_ID_635334762 A-to-I Human chr18 - 728796 728796 728796 AATGCAGCTGGGCGCAGTGGCTCAGGCCTGTAATCCCAGTACTTTGGGAGGTCGAGGCCAGTGGA AATGCAGCTGGGCGCAGTGGCTCAGGCCTGTATTCCCAGTACTTTGGGAGGTCGAGGCCAGTGGA T A YES1 Ensembl:ENSG00000176105 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1487714244 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_188211,RMVar_hsa_circ_101790,RMVar_hsa_circ_188210 14263 RMVar_ID_14263 Human_SNP_ID_635334763 A-to-I Human chr18 - 728796 728796 728796 AATGCAGCTGGGCGCAGTGGCTCAGGCCTGTAATCCCAGTACTTTGGGAGGTCGAGGCCAGTGGA AATGCAGCTGGGCGCAGTGGCTCAGGCCTGTAGTCCCAGTACTTTGGGAGGTCGAGGCCAGTGGA T C YES1 Ensembl:ENSG00000176105 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1487714244 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_188211,RMVar_hsa_circ_101790,RMVar_hsa_circ_188210 14264 RMVar_ID_14264 Human_SNP_ID_635337297 A-to-I Human chr18 - 737234 737234 737234 TGGCCAGGCTGATCTCGAACTCATGACCTCAAATGATCCACCTGCCTCGGCCTCCCAAATTAATG TGGCCAGGCTGATCTCGAACTCATGACCTCAAGTGATCCACCTGCCTCGGCCTCCCAAATTAATG T C YES1 Ensembl:ENSG00000176105 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215976641 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_188211,RMVar_hsa_circ_101790,RMVar_hsa_circ_188210,RMVar_hsa_circ_46921,RMVar_hsa_circ_327125,RMVar_hsa_circ_326286,RMVar_hsa_circ_374946,RMVar_hsa_circ_188213,RMVar_hsa_circ_375538,RMVar_hsa_circ_359835,RMVar_hsa_circ_188214,RMVar_hsa_circ_188215,RMVar_hsa_circ_188216 14265 RMVar_ID_14265 Human_SNP_ID_635352242 A-to-I Human chr18 - 793536 793536 793536 GCCTAGGAGTTTGAGACCAGCCTGAGCAATTTAGTGAGACCCCATCTCTGCAAAAAATTAAAAAA GCCTAGGAGTTTGAGACCAGCCTGAGCAATTTGGTGAGACCCCATCTCTGCAAAAAATTAAAAAA T C YES1 Ensembl:ENSG00000176105 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935757909 Functional Loss SNV dbSNP153 33..33 33 - - - 14266 RMVar_ID_14266 Human_SNP_ID_635488765 A-to-I Human chr18 - 1362762 1362762 1362762 ATTTCACATCAACCAGCCTGCTTTAAAACAGAAAGAAGCAATCCTGAAACTCATCTTGAAAAATG ATTTCACATCAACCAGCCTGCTTTAAAACAGAGAGAAGCAATCCTGAAACTCATCTTGAAAAATG T C LINC00470,AP005119.2 Ensembl:ENSG00000132204,Ensembl:ENSG00000265417 lincRNA,Pseudogene intron,exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs878868271 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2533482,Human_RBP_ID_5583295,Human_RBP_ID_17381809,Human_RBP_ID_19028684,Human_RBP_ID_20347657,Human_RBP_ID_22064141 14267 RMVar_ID_14267 Human_SNP_ID_635776819 A-to-I Human chr18 - 2560822 2560822 2560822 CCAGGCTGGAGTGCAGTGGCCCATCTCCGCTCACTGCAAACTCTGCCTCCTGGGTTCATGCCATT CCAGGCTGGAGTGCAGTGGCCCATCTCCGCTCGCTGCAAACTCTGCCTCCTGGGTTCATGCCATT T C METTL4 Ensembl:ENSG00000101574 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1046485754 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63004,RMVar_hsa_circ_188224,RMVar_hsa_circ_116581,RMVar_hsa_circ_831,RMVar_hsa_circ_310842,RMVar_hsa_circ_366807 14268 RMVar_ID_14268 Human_SNP_ID_635781777 A-to-I Human chr18 + 2580816 2580816 2580816 TGGGCTGGAGTGCAGTGGCACAATCTCGGCTCACTGCAACCTCCACCTCCCAGGTTCAAACAGTT TGGGCTGGAGTGCAGTGGCACAATCTCGGCTCGCTGCAACCTCCACCTCCCAGGTTCAAACAGTT A G NDC80 Ensembl:ENSG00000080986 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs986760100 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55789,RMVar_hsa_circ_15762,RMVar_hsa_circ_67054,RMVar_hsa_circ_70102,RMVar_hsa_circ_122161,RMVar_hsa_circ_188228 14269 RMVar_ID_14269 Human_SNP_ID_635782088 A-to-I Human chr18 + 2582146 2582146 2582146 TTGCCCAGGCTGGAATGCAGTGGCATGATCTCAGCTCACTACAATCTCCACCTCCCAGGTTCAAG TTGCCCAGGCTGGAATGCAGTGGCATGATCTCGGCTCACTACAATCTCCACCTCCCAGGTTCAAG A G NDC80 Ensembl:ENSG00000080986 Protein coding intron GSE100210;GSE99789 HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 29129909,29796672 RNA-Seq:(High) rs544359722 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1889344 RMVar_hsa_circ_55789,RMVar_hsa_circ_15762,RMVar_hsa_circ_67054,RMVar_hsa_circ_70102,RMVar_hsa_circ_122161,RMVar_hsa_circ_188228 14270 RMVar_ID_14270 Human_SNP_ID_635802675 A-to-I Human chr18 + 2660114 2660113 2660114 GGGAGGCCAAGGCGGGCGGATCACCTGAGGTCAGGAGTTAGAGATCAGCTTGGCCAACATGGTGA GGGAGGCCAAGGCGGGCGGATCACCTGAGGTC_GGAGTTAGAGATCAGCTTGGCCAACATGGTGA CA C SMCHD1 Ensembl:ENSG00000101596 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334893645 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_126636,RMVar_hsa_circ_188233 14271 RMVar_ID_14271 Human_SNP_ID_635802676 A-to-I Human chr18 + 2660114 2660114 2660114 GGGAGGCCAAGGCGGGCGGATCACCTGAGGTCAGGAGTTAGAGATCAGCTTGGCCAACATGGTGA GGGAGGCCAAGGCGGGCGGATCACCTGAGGTCGGGAGTTAGAGATCAGCTTGGCCAACATGGTGA A G SMCHD1 Ensembl:ENSG00000101596 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1357479481 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126636,RMVar_hsa_circ_188233 14272 RMVar_ID_14272 Human_SNP_ID_635805259 A-to-I Human chr18 + 2669090 2669090 2669090 AATTGTAGCTGGATGCAGTAGCTCATACCTGTAATCCCAGCACTTTGAGAGTCTGAGGCAGGAAG AATTGTAGCTGGATGCAGTAGCTCATACCTGTGATCCCAGCACTTTGAGAGTCTGAGGCAGGAAG A G SMCHD1 Ensembl:ENSG00000101596 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1336970059 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17567385 RMVar_hsa_circ_68297,RMVar_hsa_circ_352033,RMVar_hsa_circ_323318,RMVar_hsa_circ_296349,RMVar_hsa_circ_9694,RMVar_hsa_circ_20529,RMVar_hsa_circ_63949,RMVar_hsa_circ_14853,RMVar_hsa_circ_188234,RMVar_hsa_circ_5572 14273 RMVar_ID_14273 Human_SNP_ID_635819275 A-to-I Human chr18 + 2722236 2722236 2722236 GAGGCAGGTAGATAGCTGGAGCTCAGGTGTTCAAGACCAGTGTGGGCAACATGATGAGACCCTGC GAGGCAGGTAGATAGCTGGAGCTCAGGTGTTCGAGACCAGTGTGGGCAACATGATGAGACCCTGC A G SMCHD1 Ensembl:ENSG00000101596 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1484768683 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11175,RMVar_hsa_circ_68958,RMVar_hsa_circ_5572,RMVar_hsa_circ_355763,RMVar_hsa_circ_106800,RMVar_hsa_circ_110547,RMVar_hsa_circ_75805,RMVar_hsa_circ_34727,RMVar_hsa_circ_64250,RMVar_hsa_circ_47299,RMVar_hsa_circ_188235,RMVar_hsa_circ_188237,RMVar_hsa_circ_188238,RMVar_hsa_circ_188236,RMVar_hsa_circ_46759,RMVar_hsa_circ_23346,RMVar_hsa_circ_338391,RMVar_hsa_circ_342981,RMVar_hsa_circ_68910,RMVar_hsa_circ_97217,RMVar_hsa_circ_188247,RMVar_hsa_circ_188249,RMVar_hsa_circ_188248,RMVar_hsa_circ_78021,RMVar_hsa_circ_7931,RMVar_hsa_circ_36609,RMVar_hsa_circ_24604,RMVar_hsa_circ_188255,RMVar_hsa_circ_57397,RMVar_hsa_circ_60058,RMVar_hsa_circ_188256,RMVar_hsa_circ_119597,RMVar_hsa_circ_63773,RMVar_hsa_circ_359979,RMVar_hsa_circ_267448,RMVar_hsa_circ_360110,RMVar_hsa_circ_74279,RMVar_hsa_circ_14963,RMVar_hsa_circ_58425,RMVar_hsa_circ_307945,RMVar_hsa_circ_63548,RMVar_hsa_circ_122432,RMVar_hsa_circ_350287,RMVar_hsa_circ_188257,RMVar_hsa_circ_361142,RMVar_hsa_circ_340305,RMVar_hsa_circ_124289,RMVar_hsa_circ_60304,RMVar_hsa_circ_61219,RMVar_hsa_circ_188259,RMVar_hsa_circ_188258,RMVar_hsa_circ_300821,RMVar_hsa_circ_22358,RMVar_hsa_circ_58071 14274 RMVar_ID_14274 Human_SNP_ID_635831883 A-to-I Human chr18 + 2772730 2772730 2772730 GTGGCTCGCTGCTCCCTCCACCTGCTGGGCTCAAGTGATCCTTCTGCCTCAGCCCCCCAAGTAGC GTGGCTCGCTGCTCCCTCCACCTGCTGGGCTCTAGTGATCCTTCTGCCTCAGCCCCCCAAGTAGC A T SMCHD1 Ensembl:ENSG00000101596 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1410997062 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110547,RMVar_hsa_circ_188235,RMVar_hsa_circ_36609,RMVar_hsa_circ_58425,RMVar_hsa_circ_188267,RMVar_hsa_circ_15764,RMVar_hsa_circ_370023,RMVar_hsa_circ_366983,RMVar_hsa_circ_339129,RMVar_hsa_circ_62584,RMVar_hsa_circ_43434,RMVar_hsa_circ_188266,RMVar_hsa_circ_39342,RMVar_hsa_circ_14670,RMVar_hsa_circ_188275,RMVar_hsa_circ_10131,RMVar_hsa_circ_102873,RMVar_hsa_circ_376148,RMVar_hsa_circ_188281,RMVar_hsa_circ_188282,RMVar_hsa_circ_332281,RMVar_hsa_circ_326334,RMVar_hsa_circ_22662,RMVar_hsa_circ_375647,RMVar_hsa_circ_336027,RMVar_hsa_circ_316891,RMVar_hsa_circ_188288,RMVar_hsa_circ_188289,RMVar_hsa_circ_188287,RMVar_hsa_circ_298603,RMVar_hsa_circ_23804,RMVar_hsa_circ_19883,RMVar_hsa_circ_73466,RMVar_hsa_circ_376551,RMVar_hsa_circ_54295 14275 RMVar_ID_14275 Human_SNP_ID_635837007 A-to-I Human chr18 + 2793480 2793480 2793480 GGTCAGGAGATCAAGACCATCCTGGCTAACACAGTGAAACCCTGTCTCTACTAAAAATACAAAAA GGTCAGGAGATCAAGACCATCCTGGCTAACACGGTGAAACCCTGTCTCTACTAAAAATACAAAAA A G SMCHD1 Ensembl:ENSG00000101596 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1012218436 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110547,RMVar_hsa_circ_188235,RMVar_hsa_circ_15764,RMVar_hsa_circ_339129,RMVar_hsa_circ_43434,RMVar_hsa_circ_188266,RMVar_hsa_circ_188275,RMVar_hsa_circ_102873,RMVar_hsa_circ_188282,RMVar_hsa_circ_22662,RMVar_hsa_circ_336027,RMVar_hsa_circ_188289,RMVar_hsa_circ_54295,RMVar_hsa_circ_69183,RMVar_hsa_circ_334217,RMVar_hsa_circ_101136,RMVar_hsa_circ_325939,RMVar_hsa_circ_188295 14276 RMVar_ID_14276 Human_SNP_ID_635886931 A-to-I Human chr18 - 2975473 2975473 2975473 AAAATTAGCTGGGCATGGTGGCACGCGCCTGTAGTCCCGGCTACTCGAGAGGCTGAGGCAGGAGA AAAATTAGCTGGGCATGGTGGCACGCGCCTGTGGTCCCGGCTACTCGAGAGGCTGAGGCAGGAGA T C LPIN2 Ensembl:ENSG00000101577 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1567847940 Functional Loss SNV dbSNP153 33..33 33 - - - 14277 RMVar_ID_14277 Human_SNP_ID_635912853 A-to-I Human chr18 + 3070933 3070933 3070933 GGTGTGCACCACTACATTTGGCTAAATTTTGTATTTTTTGTAGAGATGGGGTTTCGTCGTGTTGC GGTGTGCACCACTACATTTGGCTAAATTTTGTGTTTTTTGTAGAGATGGGGTTTCGTCGTGTTGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1409190021 Functional Loss SNV dbSNP153 33..33 33 - - - 14278 RMVar_ID_14278 Human_SNP_ID_635981843 A-to-I Human chr18 - 3349350 3349350 3349350 TCTGTTTGTTACCCAGGCTGGAGTACAGTGGCACACTCATGGCTCACTGCAGCCCCGAGCTCCTG TCTGTTTGTTACCCAGGCTGGAGTACAGTGGCCCACTCATGGCTCACTGCAGCCCCGAGCTCCTG T G LINC01895 Ensembl:ENSG00000259256 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs938380593 Functional Loss SNV dbSNP153 33..33 33 - - - 14279 RMVar_ID_14279 Human_SNP_ID_636006667 A-to-I Human chr18 - 3446348 3446348 3446348 GAAACCCCATCTCTACTAAAAATACAAAAATTAGCCGGGCGTGGTGGCGTGTGACTGTAGTCCCA GAAACCCCATCTCTACTAAAAATACAAAAATTGGCCGGGCGTGGTGGCGTGTGACTGTAGTCCCA T C lnc-DLGAP1-11,lnc-DLGAP1-11:2,lnc-DLGAP1-11:3 RNACentral:URS0000D58A2C,RNACentral:URS0000D5901D,RNACentral:URS0000D5D483 lincRNA,lincRNA,lincRNA intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs765582772 Functional Loss SNV dbSNP153 33..33 33 - - - 14280 RMVar_ID_14280 Human_SNP_ID_636009219 A-to-I Human chr18 + 3453431 3453430 3453431 GTGCAGGGCTGGGCGCGGTGGTTCACGCCTGTAATCCCAGCACTTTGGGAGGCCTAGGCGAGCAG GTGCAGGGCTGGGCGCGGTGGTTCACGCCTGT_ATCCCAGCACTTTGGGAGGCCTAGGCGAGCAG TA T TGIF1 Ensembl:ENSG00000177426 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1440060370 Functional Loss DEL dbSNP153 33..33 33 - - - 14281 RMVar_ID_14281 Human_SNP_ID_636009220 A-to-I Human chr18 + 3453431 3453431 3453431 GTGCAGGGCTGGGCGCGGTGGTTCACGCCTGTAATCCCAGCACTTTGGGAGGCCTAGGCGAGCAG GTGCAGGGCTGGGCGCGGTGGTTCACGCCTGTTATCCCAGCACTTTGGGAGGCCTAGGCGAGCAG A T TGIF1 Ensembl:ENSG00000177426 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs892498712 Functional Loss SNV dbSNP153 33..33 33 - - - 14282 RMVar_ID_14282 Human_SNP_ID_636046819 A-to-I Human chr18 + 3598230 3598230 3598230 AAAAGTAGCTGGGCGTAGTGGCGCATGCCTGTAGTCCCAGCTGCTCGGGAGGCTGAGGCAGGAGA AAAAGTAGCTGGGCGTAGTGGCGCATGCCTGTGGTCCCAGCTGCTCGGGAGGCTGAGGCAGGAGA A G DLGAP1-AS1 Ensembl:ENSG00000177337 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs187275105 Functional Loss SNV dbSNP153 33..33 33 - - - 14283 RMVar_ID_14283 Human_SNP_ID_636047035 A-to-I Human chr18 + 3598912 3598912 3598912 CTTCTGCCTCAGCCTCCTGAGTACCTGAGACTACAGGCGGGCGCCACCACACCCGGCTAATGTTT CTTCTGCCTCAGCCTCCTGAGTACCTGAGACTGCAGGCGGGCGCCACCACACCCGGCTAATGTTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs944687439 Functional Loss SNV dbSNP153 33..33 33 - - - 14284 RMVar_ID_14284 Human_SNP_ID_636047232 A-to-I Human chr18 + 3599652 3599648 3599652 TTGTTGTTTGTTTTGTTTTTTGAGACAGTCTCACTCTGTTGTCAGGCTAGAGTGTAGTGGCGCGA TTGTTGTTTGTTTTGTTTTTTGAGACAGT____CTCTGTTGTCAGGCTAGAGTGTAGTGGCGCGA TCTCA T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749791666 Functional Loss DEL dbSNP153 30..33 33 - - - 14285 RMVar_ID_14285 Human_SNP_ID_636048225 A-to-I Human chr18 + 3601118 3601118 3601118 ATAGATATATATATTTTTTGAGACAGAGTCTCACCCTGTGGCTCAGGCTAGAGTGCAGTGATGTG ATAGATATATATATTTTTTGAGACAGAGTCTCCCCCTGTGGCTCAGGCTAGAGTGCAGTGATGTG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1261369747 Functional Loss SNV dbSNP153 33..33 33 - - - 14286 RMVar_ID_14286 Human_SNP_ID_636048250 A-to-I Human chr18 + 3601204 3601204 3601204 CACTTCCCGGGCTAAAGCAATTCTCCCACCTCAGCCACCCAAGTAGCTGGGATTACAGGCACCTG CACTTCCCGGGCTAAAGCAATTCTCCCACCTCGGCCACCCAAGTAGCTGGGATTACAGGCACCTG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1390197136 Functional Loss SNV dbSNP153 33..33 33 - - - 14287 RMVar_ID_14287 Human_SNP_ID_636048356 A-to-I Human chr18 + 3601585 3601585 3601585 AAACCTACGGCTGGGCATGGTGGTTCACGCCTATAATCCCAGCACTTTGGGAGGCCGAGGTGGGC AAACCTACGGCTGGGCATGGTGGTTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1366596568 Functional Loss SNV dbSNP153 33..33 33 - - - 14288 RMVar_ID_14288 Human_SNP_ID_636048479 A-to-I Human chr18 + 3601937 3601937 3601937 AGGCTGAGGCAGGCGAATCGCTTGAACCCGGGAAGCGGAGATTGCAGTGAGTGGAGATCGGGCCA AGGCTGAGGCAGGCGAATCGCTTGAACCCGGGGAGCGGAGATTGCAGTGAGTGGAGATCGGGCCA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs12960382 Functional Loss SNV dbSNP153 33..33 33 - - - 14289 RMVar_ID_14289 Human_SNP_ID_636048480 A-to-I Human chr18 + 3601937 3601937 3601937 AGGCTGAGGCAGGCGAATCGCTTGAACCCGGGAAGCGGAGATTGCAGTGAGTGGAGATCGGGCCA AGGCTGAGGCAGGCGAATCGCTTGAACCCGGGTAGCGGAGATTGCAGTGAGTGGAGATCGGGCCA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs12960382 Functional Loss SNV dbSNP153 33..33 33 - - - 14290 RMVar_ID_14290 Human_SNP_ID_636049837 A-to-I Human chr18 + 3606937 3606937 3606937 TCGGCTCATTGCAACCTCCACCTCCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCCAGTAGC TCGGCTCATTGCAACCTCCACCTCCCGGGTTCGAGCAATTCTCCTGCCTCAGCCTCCCCAGTAGC A G DLGAP1-AS2 Ensembl:ENSG00000262001 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs769700721 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_136780 14291 RMVar_ID_14291 Human_SNP_ID_636049858 A-to-I Human chr18 + 3607012 3607012 3607012 GGCACCTGCCACCACACCTGGCTAATTTTAGTAGAGAAGGGGTTTCGCCAAGCTGGCCAGGCTGG GGCACCTGCCACCACACCTGGCTAATTTTAGTGGAGAAGGGGTTTCGCCAAGCTGGCCAGGCTGG A G DLGAP1-AS2 Ensembl:ENSG00000262001 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1056704580 Functional Loss SNV dbSNP153 33..33 33 - - - 14292 RMVar_ID_14292 Human_SNP_ID_636049935 A-to-I Human chr18 + 3607330 3607330 3607330 AGGCCGGTGCCACCACACCCAGATAATATTTTATATTTTTTGTAGAAATGGGGTTTTGTTTTGTT AGGCCGGTGCCACCACACCCAGATAATATTTTGTATTTTTTGTAGAAATGGGGTTTTGTTTTGTT A G DLGAP1-AS2 Ensembl:ENSG00000262001 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1203129215 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13302035 14293 RMVar_ID_14293 Human_SNP_ID_636050120 A-to-I Human chr18 + 3608121 3608121 3608121 GATGCGGGCAGATCATGTGAAGTCGGGAGTTCAAGACCAGCCTGACCAACATGGAGAAGCCCTGT GATGCGGGCAGATCATGTGAAGTCGGGAGTTCGAGACCAGCCTGACCAACATGGAGAAGCCCTGT A G DLGAP1-AS2 Ensembl:ENSG00000262001 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1327887873 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_136952,Human_RBP_ID_22064164 14294 RMVar_ID_14294 Human_SNP_ID_636050144 A-to-I Human chr18 + 3608201 3608201 3608201 AAAATTAGCCGGGTGTGGTGGCGCATGCCTGTAATTCTAGCTACTGGGGAGGCTGAGGCAGGAGA AAAATTAGCCGGGTGTGGTGGCGCATGCCTGTGATTCTAGCTACTGGGGAGGCTGAGGCAGGAGA A G DLGAP1-AS2 Ensembl:ENSG00000262001 lincRNA exon GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs977694273 Functional Loss SNV dbSNP153 33..33 33 - - - 14295 RMVar_ID_14295 Human_SNP_ID_636060452 A-to-I Human chr18 - 3647191 3647191 3647191 GGAGTGCAATGGCACAATCTCAGCTCACTCCAACCTGCGCCTCCCAGGTTCAAGCGATTCTCCTG GGAGTGCAATGGCACAATCTCAGCTCACTCCAGCCTGCGCCTCCCAGGTTCAAGCGATTCTCCTG T C DLGAP1 Ensembl:ENSG00000170579 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1053541196 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 14296 RMVar_ID_14296 Human_SNP_ID_636071145 A-to-I Human chr18 - 3690179 3690179 3690179 GGAAGACTGAAGTGGGAGGATCACTTAAGCCCAGGAGTTCGAGTCCGCAGTGAGCTGTGATTGCA GGAAGACTGAAGTGGGAGGATCACTTAAGCCCTGGAGTTCGAGTCCGCAGTGAGCTGTGATTGCA T A DLGAP1 Ensembl:ENSG00000170579 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1183443865 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2814,RMVar_hsa_circ_44870,RMVar_hsa_circ_48231,RMVar_hsa_circ_20885,RMVar_hsa_circ_20087 14297 RMVar_ID_14297 Human_SNP_ID_636071146 A-to-I Human chr18 - 3690179 3690179 3690179 GGAAGACTGAAGTGGGAGGATCACTTAAGCCCAGGAGTTCGAGTCCGCAGTGAGCTGTGATTGCA GGAAGACTGAAGTGGGAGGATCACTTAAGCCCCGGAGTTCGAGTCCGCAGTGAGCTGTGATTGCA T G DLGAP1 Ensembl:ENSG00000170579 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1183443865 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2814,RMVar_hsa_circ_44870,RMVar_hsa_circ_48231,RMVar_hsa_circ_20885,RMVar_hsa_circ_20087 14298 RMVar_ID_14298 Human_SNP_ID_636071147 A-to-I Human chr18 - 3690185 3690185 3690185 CTACTTGGAAGACTGAAGTGGGAGGATCACTTAAGCCCAGGAGTTCGAGTCCGCAGTGAGCTGTG CTACTTGGAAGACTGAAGTGGGAGGATCACTTGAGCCCAGGAGTTCGAGTCCGCAGTGAGCTGTG T C DLGAP1 Ensembl:ENSG00000170579 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs960805054 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2814,RMVar_hsa_circ_44870,RMVar_hsa_circ_48231,RMVar_hsa_circ_20885,RMVar_hsa_circ_20087 14299 RMVar_ID_14299 Human_SNP_ID_636071151 A-to-I Human chr18 - 3690218 3690218 3690218 GCCGGGCTTCATGACACATGCCTGCAGTCCCAACTACTTGGAAGACTGAAGTGGGAGGATCACTT GCCGGGCTTCATGACACATGCCTGCAGTCCCAGCTACTTGGAAGACTGAAGTGGGAGGATCACTT T C DLGAP1 Ensembl:ENSG00000170579 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1282929209 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2814,RMVar_hsa_circ_44870,RMVar_hsa_circ_48231,RMVar_hsa_circ_20885,RMVar_hsa_circ_20087 14300 RMVar_ID_14300 Human_SNP_ID_636071152 A-to-I Human chr18 - 3690218 3690218 3690218 GCCGGGCTTCATGACACATGCCTGCAGTCCCAACTACTTGGAAGACTGAAGTGGGAGGATCACTT GCCGGGCTTCATGACACATGCCTGCAGTCCCACCTACTTGGAAGACTGAAGTGGGAGGATCACTT T G DLGAP1 Ensembl:ENSG00000170579 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1282929209 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2814,RMVar_hsa_circ_44870,RMVar_hsa_circ_48231,RMVar_hsa_circ_20885,RMVar_hsa_circ_20087 14301 RMVar_ID_14301 Human_SNP_ID_636097329 A-to-I Human chr18 - 3797831 3797831 3797831 ACACGTGGAAATTATGGGAGCTACTATTCAAGATGAGATTTGGGTGGGGACACAGCAAAACCATA ACACGTGGAAATTATGGGAGCTACTATTCAAGGTGAGATTTGGGTGGGGACACAGCAAAACCATA T C DLGAP1 Ensembl:ENSG00000170579 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1286575531 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44870,RMVar_hsa_circ_32290,RMVar_hsa_circ_20087 14302 RMVar_ID_14302 Human_SNP_ID_636147142 A-to-I Human chr18 + 4006738 4006738 4006738 CACGATCACAGCTCACTGCATCCTTGACCCCCAGTGTTCAAGTGATCCTTCTACCTCACCCTCTC CACGATCACAGCTCACTGCATCCTTGACCCCCGGTGTTCAAGTGATCCTTCTACCTCACCCTCTC A G DLGAP1-AS4 Ensembl:ENSG00000263878 lincRNA intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs956892302 Functional Loss SNV dbSNP153 33..33 33 - - - 14303 RMVar_ID_14303 Human_SNP_ID_636221010 A-to-I Human chr18 - 4317972 4317972 4317972 GTGATGGTACGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCCGGAGAATCGTTTGAACCCA GTGATGGTACGCGCCTGTAATCCCAGCTACTCTGGAGGCTGAGGCCGGAGAATCGTTTGAACCCA T A DLGAP1 Ensembl:ENSG00000170579 Protein coding intron GSE107867 ASD brains,cerebellum;ASD brains,frontal_cortex;ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs569408048 Functional Loss SNV dbSNP153 33..33 33 - - - 14304 RMVar_ID_14304 Human_SNP_ID_636224782 A-to-I Human chr18 - 4333850 4333850 4333850 CACGCCTGTGGTCCCGGCACTTTGGGAGGCCAAGGCGGGCGGATCACGAGGTTAGGAGATAGAGA CACGCCTGTGGTCCCGGCACTTTGGGAGGCCAGGGCGGGCGGATCACGAGGTTAGGAGATAGAGA T C DLGAP1 Ensembl:ENSG00000170579 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1260721905 Functional Loss SNV dbSNP153 33..33 33 - - - 14305 RMVar_ID_14305 Human_SNP_ID_636464893 A-to-I Human chr18 - 5294443 5294443 5294443 AAAACAACAACAACACATTGATATGTTGTCATAGCTAGTCTAAGGCCACTCCTCTCTCTGGTCCC AAAACAACAACAACACATTGATATGTTGTCATGGCTAGTCTAAGGCCACTCCTCTCTCTGGTCCC T C ZBTB14 Ensembl:ENSG00000198081 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934908960 Functional Loss SNV dbSNP153 33..33 33 - - - 14306 RMVar_ID_14306 Human_SNP_ID_636536889 A-to-I Human chr18 - 5577142 5577142 5577142 AAATGTTTGTTATTTATGTCTTTGCTACGCTAATTGTTCTCTAGTTTTTCTCTGATTTGAAAGCT AAATGTTTGTTATTTATGTCTTTGCTACGCTAGTTGTTCTCTAGTTTTTCTCTGATTTGAAAGCT T C EPB41L3 Ensembl:ENSG00000082397 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1291219731 Functional Loss SNV dbSNP153 33..33 33 - - - 14307 RMVar_ID_14307 Human_SNP_ID_636892777 A-to-I Human chr18 - 6997365 6997365 6997365 AGCTGCCCTATTAGAAAAGCAGAAAATAGGCCAGGCACGGTGGCTCACACCTGTAATCCCAGCAT AGCTGCCCTATTAGAAAAGCAGAAAATAGGCCGGGCACGGTGGCTCACACCTGTAATCCCAGCAT T C LAMA1 Ensembl:ENSG00000101680 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1184011471 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29313,RMVar_hsa_circ_105922,RMVar_hsa_circ_188392,RMVar_hsa_circ_89096,RMVar_hsa_circ_78594,RMVar_hsa_circ_188393,RMVar_hsa_circ_101368,RMVar_hsa_circ_188394,RMVar_hsa_circ_188395,RMVar_hsa_circ_99906,RMVar_hsa_circ_97602,RMVar_hsa_circ_339991,RMVar_hsa_circ_188399,RMVar_hsa_circ_43245,RMVar_hsa_circ_188401,RMVar_hsa_circ_87091,RMVar_hsa_circ_188400,RMVar_hsa_circ_333865,RMVar_hsa_circ_188402,RMVar_hsa_circ_33487 14308 RMVar_ID_14308 Human_SNP_ID_636894691 A-to-I Human chr18 - 7004455 7004455 7004455 CCAGCTGCTCGGGAGGCTGGGGCAGAAGAATCACTTGAACCCAGGAGGCAGAGGTTGCGGTGAGC CCAGCTGCTCGGGAGGCTGGGGCAGAAGAATCCCTTGAACCCAGGAGGCAGAGGTTGCGGTGAGC T G LAMA1 Ensembl:ENSG00000101680 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs925800458 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89096,RMVar_hsa_circ_78594,RMVar_hsa_circ_188393,RMVar_hsa_circ_101368,RMVar_hsa_circ_188394,RMVar_hsa_circ_188395,RMVar_hsa_circ_99906,RMVar_hsa_circ_97602,RMVar_hsa_circ_188399,RMVar_hsa_circ_43245,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_370354,RMVar_hsa_circ_188403,RMVar_hsa_circ_188404 14309 RMVar_ID_14309 Human_SNP_ID_637044682 A-to-I Human chr18 + 7573612 7573612 7573612 TTTGTTTTGTTTTGTTTTGTTTTTTTTGAGACAAAGTCTCGCTCTTGTCCCCCAGGCTAGAGTGC TTTGTTTTGTTTTGTTTTGTTTTTTTTGAGACGAAGTCTCGCTCTTGTCCCCCAGGCTAGAGTGC A G PTPRM Ensembl:ENSG00000173482 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs554485913 Functional Loss SNV dbSNP153 33..33 33 - - - 14310 RMVar_ID_14310 Human_SNP_ID_637044689 A-to-I Human chr18 + 7573638 7573638 7573638 TGAGACAAAGTCTCGCTCTTGTCCCCCAGGCTAGAGTGCAACTGAGTGATATTGGCTCACTACAA TGAGACAAAGTCTCGCTCTTGTCCCCCAGGCTGGAGTGCAACTGAGTGATATTGGCTCACTACAA A G PTPRM Ensembl:ENSG00000173482 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs754433269 Functional Loss SNV dbSNP153 33..33 33 - - - 14311 RMVar_ID_14311 Human_SNP_ID_637074155 A-to-I Human chr18 + 7701193 7701193 7701193 GGGCATGGTGGCATGTGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCTTGAA GGGCATGGTGGCATGTGCCTGTAGTCCCAGCTGCTCGGGAGGCTGAGGCAGGAGAATTGCTTGAA A G PTPRM Ensembl:ENSG00000173482 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1471916015 Functional Loss SNV dbSNP153 33..33 33 - - - 14312 RMVar_ID_14312 Human_SNP_ID_637298223 A-to-I Human chr18 + 8619873 8619873 8619873 GGAAATTAAGGTCAAGAATAAGACACCGGCACAGTTGCTCATGCCTATAAACCCAGCACTTGGAG GGAAATTAAGGTCAAGAATAAGACACCGGCACGGTTGCTCATGCCTATAAACCCAGCACTTGGAG A G RAB12 Ensembl:ENSG00000206418 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs901644577 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13343393 14313 RMVar_ID_14313 Human_SNP_ID_637298260 A-to-I Human chr18 + 8620013 8620013 8620013 AAAATCAGTTAGTGACAGTGGTGTGCTTCTGTAGACTCAGGTACTCGGGAGGCTGAGGTGGGAGG AAAATCAGTTAGTGACAGTGGTGTGCTTCTGTGGACTCAGGTACTCGGGAGGCTGAGGTGGGAGG A G RAB12 Ensembl:ENSG00000206418 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs958851535 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13343401 14314 RMVar_ID_14314 Human_SNP_ID_637300885 A-to-I Human chr18 + 8631072 8631072 8631072 CATCATGCCTAGCTAAGTTTTATATTTTTAGTAGAGACGGGGGTTTCACCATGTTGGCCAGGCTG CATCATGCCTAGCTAAGTTTTATATTTTTAGTGGAGACGGGGGTTTCACCATGTTGGCCAGGCTG A G RAB12 Ensembl:ENSG00000206418 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs568817745 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_334645,RMVar_hsa_circ_377807,RMVar_hsa_circ_124154,RMVar_hsa_circ_328888,RMVar_hsa_circ_188475,RMVar_hsa_circ_188476 14315 RMVar_ID_14315 Human_SNP_ID_637301087 A-to-I Human chr18 + 8632013 8632013 8632013 TTGGTTTGAAAGTAATTGGAGGCTGGGCTGGTAGCTTACACCTGTAATTCCAGCACTTTGGGAGG TTGGTTTGAAAGTAATTGGAGGCTGGGCTGGTGGCTTACACCTGTAATTCCAGCACTTTGGGAGG A G RAB12 Ensembl:ENSG00000206418 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1259846004 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_334645,RMVar_hsa_circ_377807,RMVar_hsa_circ_124154,RMVar_hsa_circ_328888,RMVar_hsa_circ_188475,RMVar_hsa_circ_188476 14316 RMVar_ID_14316 Human_SNP_ID_637301935 A-to-I Human chr18 + 8635550 8635550 8635550 TTTAAAATTCCACAGTATGCTTCAGAAGATGCAGAGCTTCTCTTAGTTGGAAATAAGTTGGACTG TTTAAAATTCCACAGTATGCTTCAGAAGATGCGGAGCTTCTCTTAGTTGGAAATAAGTTGGACTG A G RAB12 Ensembl:ENSG00000206418 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1207061658 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_511288,Human_RBP_ID_6708186,Human_RBP_ID_26334540 Human_Splice_Rec_1893012,Human_Splice_Rec_1893013,Human_Splice_Rec_1893022,Human_Splice_Rec_1893023,Human_Splice_Rec_1893028 Human_miRNA_ID_2396135 RMVar_hsa_circ_29033,RMVar_hsa_circ_334645,RMVar_hsa_circ_377807,RMVar_hsa_circ_124154,RMVar_hsa_circ_328888,RMVar_hsa_circ_188475,RMVar_hsa_circ_188476,RMVar_hsa_circ_58640 14317 RMVar_ID_14317 Human_SNP_ID_637346940 A-to-I Human chr18 + 8804893 8804893 8804893 CACGCCTGTAGTCCCAGCTACTTGGGAGTGTGAGGTGGGAGGACTGCTTGAGCCCAGGAGGTTGA CACGCCTGTAGTCCCAGCTACTTGGGAGTGTGGGGTGGGAGGACTGCTTGAGCCCAGGAGGTTGA A G MTCL1 Ensembl:ENSG00000168502 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1338785551 Functional Loss SNV dbSNP153 33..33 33 - - - 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_352467,RMVar_hsa_circ_37579,RMVar_hsa_circ_295583,RMVar_hsa_circ_46534 14318 RMVar_ID_14318 Human_SNP_ID_637425550 A-to-I Human chr18 + 9110528 9110526 9110528 TCTTTATTGTTTGTTTACTTACTACTTTTTTGAGACAGGGTCTCACTCTGTCTCCCAGGCTTGGG TCTTTATTGTTTGTTTACTTACTACTTTTTT__GACAGGGTCTCACTCTGTCTCCCAGGCTTGGG TGA T NDUFV2,AP005263.1 Ensembl:ENSG00000178127,Ensembl:ENSG00000265257 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs932658170 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_3560518,Human_RBP_ID_6708465,Human_RBP_ID_9906015,Human_RBP_ID_13344830 RMVar_hsa_circ_90266,RMVar_hsa_circ_188493 14319 RMVar_ID_14319 Human_SNP_ID_637425556 A-to-I Human chr18 + 9110540 9110540 9110540 GTTTACTTACTACTTTTTTGAGACAGGGTCTCACTCTGTCTCCCAGGCTTGGGTGCAGTGCATGA GTTTACTTACTACTTTTTTGAGACAGGGTCTCGCTCTGTCTCCCAGGCTTGGGTGCAGTGCATGA A G NDUFV2,AP005263.1 Ensembl:ENSG00000178127,Ensembl:ENSG00000265257 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037646887 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_768831,Human_RBP_ID_9906015,Human_RBP_ID_13344830 RMVar_hsa_circ_90266,RMVar_hsa_circ_188493 14320 RMVar_ID_14320 Human_SNP_ID_637425557 A-to-I Human chr18 + 9110540 9110540 9110540 GTTTACTTACTACTTTTTTGAGACAGGGTCTCACTCTGTCTCCCAGGCTTGGGTGCAGTGCATGA GTTTACTTACTACTTTTTTGAGACAGGGTCTCTCTCTGTCTCCCAGGCTTGGGTGCAGTGCATGA A T NDUFV2,AP005263.1 Ensembl:ENSG00000178127,Ensembl:ENSG00000265257 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037646887 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_768831,Human_RBP_ID_9906015,Human_RBP_ID_13344830 RMVar_hsa_circ_90266,RMVar_hsa_circ_188493 14321 RMVar_ID_14321 Human_SNP_ID_637425578 A-to-I Human chr18 + 9110647 9110647 9110647 CTCCCACCTCAGCCTCTCAAGTGGCTGGGACTACAGGCATGTGCCACCATGCCTGGCTAACTTTT CTCCCACCTCAGCCTCTCAAGTGGCTGGGACTTCAGGCATGTGCCACCATGCCTGGCTAACTTTT A T NDUFV2,AP005263.1 Ensembl:ENSG00000178127,Ensembl:ENSG00000265257 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1331969899 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90266,RMVar_hsa_circ_188493 14322 RMVar_ID_14322 Human_SNP_ID_637425579 A-to-I Human chr18 + 9110660 9110660 9110660 CTCTCAAGTGGCTGGGACTACAGGCATGTGCCACCATGCCTGGCTAACTTTTGTATTTTTTGTAG CTCTCAAGTGGCTGGGACTACAGGCATGTGCCGCCATGCCTGGCTAACTTTTGTATTTTTTGTAG A G NDUFV2,AP005263.1 Ensembl:ENSG00000178127,Ensembl:ENSG00000265257 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1303666349 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90266,RMVar_hsa_circ_188493 14323 RMVar_ID_14323 Human_SNP_ID_637425774 A-to-I Human chr18 + 9111528 9111528 9111528 TGGGCTCACTGCAACCTCTGCATCCTGAGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGGTTAGC TGGGCTCACTGCAACCTCTGCATCCTGAGTTCTAGCGATTCTCCTGCCTCAGCCTCCTGGTTAGC A T NDUFV2,AP005263.1 Ensembl:ENSG00000178127,Ensembl:ENSG00000265257 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1299568784 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90266,RMVar_hsa_circ_188493 14324 RMVar_ID_14324 Human_SNP_ID_637434449 A-to-I Human chr18 + 9143560 9143560 9143560 TTGGCGTACTGCAACCTCCGCCTCCTGGTTTCAAGCGATTCTCCTGCCCCAGCTCCCCGAGGAGC TTGGCGTACTGCAACCTCCGCCTCCTGGTTTCCAGCGATTCTCCTGCCCCAGCTCCCCGAGGAGC A C ANKRD12,AP005263.1 Ensembl:ENSG00000101745,Ensembl:ENSG00000265257 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1451282132 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104670,RMVar_hsa_circ_188503 14325 RMVar_ID_14325 Human_SNP_ID_637450214 A-to-I Human chr18 + 9199029 9199029 9199029 AAATAATGTAGTAAGGCTGGGCATGGTGGCTCACACCTGAAATCCCAGCACTTTGGAAGGCCAAG AAATAATGTAGTAAGGCTGGGCATGGTGGCTCCCACCTGAAATCCCAGCACTTTGGAAGGCCAAG A C ANKRD12,AP005263.1 Ensembl:ENSG00000101745,Ensembl:ENSG00000265257 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1453845437 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13915,RMVar_hsa_circ_292312,RMVar_hsa_circ_104670,RMVar_hsa_circ_188503,RMVar_hsa_circ_297667,RMVar_hsa_circ_287580,RMVar_hsa_circ_275930,RMVar_hsa_circ_40783,RMVar_hsa_circ_54211,RMVar_hsa_circ_31709,RMVar_hsa_circ_112554,RMVar_hsa_circ_188507,RMVar_hsa_circ_188511,RMVar_hsa_circ_188513,RMVar_hsa_circ_188514,RMVar_hsa_circ_188512,RMVar_hsa_circ_188509,RMVar_hsa_circ_188510,RMVar_hsa_circ_188508,RMVar_hsa_circ_357267,RMVar_hsa_circ_188505,RMVar_hsa_circ_188506,RMVar_hsa_circ_188504,RMVar_hsa_circ_366747,RMVar_hsa_circ_313040,RMVar_hsa_circ_313603,RMVar_hsa_circ_273759,RMVar_hsa_circ_188518,RMVar_hsa_circ_62204,RMVar_hsa_circ_73090,RMVar_hsa_circ_188520,RMVar_hsa_circ_188521,RMVar_hsa_circ_188522,RMVar_hsa_circ_188519,RMVar_hsa_circ_188516,RMVar_hsa_circ_188517,RMVar_hsa_circ_188523 14326 RMVar_ID_14326 Human_SNP_ID_637471339 A-to-I Human chr18 + 9276599 9276599 9276599 AACTGGGTGTGGTGGGGCACACATGTAGTCCCAGCTACCAGGGAGGCTGAGGTAGGAGGATCTGT AACTGGGTGTGGTGGGGCACACATGTAGTCCCTGCTACCAGGGAGGCTGAGGTAGGAGGATCTGT A T ANKRD12 Ensembl:ENSG00000101745 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1275492475 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104670,RMVar_hsa_circ_188503,RMVar_hsa_circ_62204,RMVar_hsa_circ_76902,RMVar_hsa_circ_188541,RMVar_hsa_circ_13134,RMVar_hsa_circ_304966 14327 RMVar_ID_14327 Human_SNP_ID_637492487 A-to-I Human chr18 + 9365282 9365282 9365282 AGGTCAAGGCTGCAGTGAGCTCTGATTGCACTACAGCACTCCAGCCTGGGCAACAGAGTAAGACC AGGTCAAGGCTGCAGTGAGCTCTGATTGCACTGCAGCACTCCAGCCTGGGCAACAGAGTAAGACC A G TWSG1 Ensembl:ENSG00000128791 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1397956447 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9906305 RMVar_hsa_circ_22861,RMVar_hsa_circ_87466,RMVar_hsa_circ_188546 14328 RMVar_ID_14328 Human_SNP_ID_637492928 A-to-I Human chr18 + 9367137 9367137 9367137 AATTTTTTGTAGAGATGGGGTCTCAATGTGTTATCCAGACTGGTCTTGAATTCCTGGACACAAGT AATTTTTTGTAGAGATGGGGTCTCAATGTGTTTTCCAGACTGGTCTTGAATTCCTGGACACAAGT A T TWSG1 Ensembl:ENSG00000128791 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1374324958 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_188547,RMVar_hsa_circ_22861,RMVar_hsa_circ_87466,RMVar_hsa_circ_188546 14329 RMVar_ID_14329 Human_SNP_ID_637493301 A-to-I Human chr18 + 9368827 9368827 9368827 AAAATTAGCTGGGCATGGTGGCACACACCTGTAATCCCAGCTATTCGGGAGGCTGAGGCAGGAGA AAAATTAGCTGGGCATGGTGGCACACACCTGTGATCCCAGCTATTCGGGAGGCTGAGGCAGGAGA A G TWSG1 Ensembl:ENSG00000128791 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1297483141 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_188547,RMVar_hsa_circ_22861,RMVar_hsa_circ_87466,RMVar_hsa_circ_188546,RMVar_hsa_circ_188548 14330 RMVar_ID_14330 Human_SNP_ID_637493445 A-to-I Human chr18 + 9369288 9369288 9369288 TGTCTATTCTGATCCTTTGCCCGTTTCTTTTGAGTCAGAGTCTTGCTCTGTCACCCAGGCTAGAG TGTCTATTCTGATCCTTTGCCCGTTTCTTTTGGGTCAGAGTCTTGCTCTGTCACCCAGGCTAGAG A G TWSG1 Ensembl:ENSG00000128791 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs761476645 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_188547,RMVar_hsa_circ_22861,RMVar_hsa_circ_87466,RMVar_hsa_circ_188546,RMVar_hsa_circ_188548 14331 RMVar_ID_14331 Human_SNP_ID_637493496 A-to-I Human chr18 + 9369546 9369546 9369546 ACCTCGCCTTCCCAAATGCTGGGATTACAGGCATGAGCCACCGCACCTGGGCCCTTTGCCCATTT ACCTCGCCTTCCCAAATGCTGGGATTACAGGCGTGAGCCACCGCACCTGGGCCCTTTGCCCATTT A G TWSG1 Ensembl:ENSG00000128791 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1321438687 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_188547,RMVar_hsa_circ_22861,RMVar_hsa_circ_87466,RMVar_hsa_circ_188546,RMVar_hsa_circ_188548 14332 RMVar_ID_14332 Human_SNP_ID_637493607 A-to-I Human chr18 + 9370058 9370058 9370058 GAATCATTGTCCAGCCAGGCGCAGTGGTTCACACCTGTAATACCAGCATTTTGGGAGGCTGAGGT GAATCATTGTCCAGCCAGGCGCAGTGGTTCACGCCTGTAATACCAGCATTTTGGGAGGCTGAGGT A G TWSG1 Ensembl:ENSG00000128791 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1482464424 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_188547,RMVar_hsa_circ_22861,RMVar_hsa_circ_87466,RMVar_hsa_circ_188546,RMVar_hsa_circ_188548 14333 RMVar_ID_14333 Human_SNP_ID_637496622 A-to-I Human chr18 + 9383294 9383294 9383294 TTGGCCACTGCAGACTCCGCCTCCCAGGTTCAAACGATTCTCCTGCCTCAGCCTCCTGAGTGGCT TTGGCCACTGCAGACTCCGCCTCCCAGGTTCAGACGATTCTCCTGCCTCAGCCTCCTGAGTGGCT A G TWSG1 Ensembl:ENSG00000128791 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1326692762 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_188547,RMVar_hsa_circ_22861,RMVar_hsa_circ_87466,RMVar_hsa_circ_188546,RMVar_hsa_circ_188548 14334 RMVar_ID_14334 Human_SNP_ID_637498345 A-to-I Human chr18 + 9390754 9390754 9390754 CAAAATTAGGCCAGGTGCAGTGGTTCATGTCTATAAACCCAGAGCTTTGGAAATCTGAGACAGAA CAAAATTAGGCCAGGTGCAGTGGTTCATGTCTGTAAACCCAGAGCTTTGGAAATCTGAGACAGAA A G TWSG1 Ensembl:ENSG00000128791 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941790500 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22861,RMVar_hsa_circ_87466,RMVar_hsa_circ_188546,RMVar_hsa_circ_30226 14335 RMVar_ID_14335 Human_SNP_ID_637500343 A-to-I Human chr18 + 9399575 9399575 9399575 ACCAAAGCAACTTAGTAAAATAATAGGTATAAAAAGTTATTCTGTAAGTCTGTTGGTTGTATCTT ACCAAAGCAACTTAGTAAAATAATAGGTATAAGAAGTTATTCTGTAAGTCTGTTGGTTGTATCTT A G TWSG1 Ensembl:ENSG00000128791 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs775778823 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_511426,Human_RBP_ID_2553065,Human_RBP_ID_3560730,Human_RBP_ID_23779585 Human_miRNA_ID_2745845 RMVar_hsa_circ_87466,RMVar_hsa_circ_188546 14336 RMVar_ID_14336 Human_SNP_ID_637528820 A-to-I Human chr18 + 9518619 9518619 9518619 TAAAGTTAATTGTTGGCTGAGGCAGGAGGATCACTTGAACCCAGGAGTTTGAGGCTGCAGTGAGC TAAAGTTAATTGTTGGCTGAGGCAGGAGGATCGCTTGAACCCAGGAGTTTGAGGCTGCAGTGAGC A G RALBP1 Ensembl:ENSG00000017797 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1313248141 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5144585,Human_RBP_ID_13346213,Human_RBP_ID_26463455 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 14337 RMVar_ID_14337 Human_SNP_ID_637531826 A-to-I Human chr18 + 9531001 9531000 9531002 GCAAGACTCTTTTTTGTTTTTGTTTTTGAGACAAAGTCTCGCTCTTGTCCCCCAGGCTGGAGTGC GCAAGACTCTTTTTTGTTTTTGTTTTTGAGAC__AGTCTCGCTCTTGTCCCCCAGGCTGGAGTGC CAA C RALBP1 Ensembl:ENSG00000017797 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1446862803 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_124665,RMVar_hsa_circ_188551,RMVar_hsa_circ_56633,RMVar_hsa_circ_42048 14338 RMVar_ID_14338 Human_SNP_ID_637531856 A-to-I Human chr18 + 9531079 9531079 9531079 CGGCTCACTGCAACCTGCAACCTCCGCCTCCCAGGCTCAAGCGATTCTCCTGCCTCGGCCCCCTG CGGCTCACTGCAACCTGCAACCTCCGCCTCCCGGGCTCAAGCGATTCTCCTGCCTCGGCCCCCTG A G RALBP1 Ensembl:ENSG00000017797 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334473395 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124665,RMVar_hsa_circ_188551,RMVar_hsa_circ_56633,RMVar_hsa_circ_42048 14339 RMVar_ID_14339 Human_SNP_ID_637538530 A-to-I Human chr18 - 9555085 9555085 9555085 TTGCCCACACTGGTCTTGAACTCCTGGGCTCAAGTGATCTGCCCCGCCTTAGCCTCCCAAAGTTC TTGCCCACACTGGTCTTGAACTCCTGGGCTCAGGTGATCTGCCCCGCCTTAGCCTCCCAAAGTTC T C PPP4R1 Ensembl:ENSG00000154845 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215613722 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2031,RMVar_hsa_circ_77469,RMVar_hsa_circ_122761,RMVar_hsa_circ_86661,RMVar_hsa_circ_67544,RMVar_hsa_circ_188559,RMVar_hsa_circ_188560,RMVar_hsa_circ_188558,RMVar_hsa_circ_320717,RMVar_hsa_circ_268523,RMVar_hsa_circ_318771,RMVar_hsa_circ_349240,RMVar_hsa_circ_351201,RMVar_hsa_circ_294948,RMVar_hsa_circ_11433,RMVar_hsa_circ_188562,RMVar_hsa_circ_188563,RMVar_hsa_circ_188561 14340 RMVar_ID_14340 Human_SNP_ID_637538531 A-to-I Human chr18 - 9555086 9555086 9555086 GTTGCCCACACTGGTCTTGAACTCCTGGGCTCAAGTGATCTGCCCCGCCTTAGCCTCCCAAAGTT GTTGCCCACACTGGTCTTGAACTCCTGGGCTCGAGTGATCTGCCCCGCCTTAGCCTCCCAAAGTT T C PPP4R1 Ensembl:ENSG00000154845 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs545355532 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2031,RMVar_hsa_circ_77469,RMVar_hsa_circ_122761,RMVar_hsa_circ_86661,RMVar_hsa_circ_67544,RMVar_hsa_circ_188559,RMVar_hsa_circ_188560,RMVar_hsa_circ_188558,RMVar_hsa_circ_320717,RMVar_hsa_circ_268523,RMVar_hsa_circ_318771,RMVar_hsa_circ_349240,RMVar_hsa_circ_351201,RMVar_hsa_circ_294948,RMVar_hsa_circ_11433,RMVar_hsa_circ_188562,RMVar_hsa_circ_188563,RMVar_hsa_circ_188561 14341 RMVar_ID_14341 Human_SNP_ID_637544327 A-to-I Human chr18 - 9577499 9577499 9577499 CACCACGCCCTGCTAACTTTGGTATTTTTTGTAGAGACTGGATTTCGCCATGTTGCCCAGGCTGG CACCACGCCCTGCTAACTTTGGTATTTTTTGTGGAGACTGGATTTCGCCATGTTGCCCAGGCTGG T C PPP4R1 Ensembl:ENSG00000154845 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904590405 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25375890 RMVar_hsa_circ_2031,RMVar_hsa_circ_77469,RMVar_hsa_circ_122761,RMVar_hsa_circ_188559,RMVar_hsa_circ_188560,RMVar_hsa_circ_320717,RMVar_hsa_circ_268523,RMVar_hsa_circ_318771,RMVar_hsa_circ_351201,RMVar_hsa_circ_17338,RMVar_hsa_circ_14714,RMVar_hsa_circ_294245,RMVar_hsa_circ_188562,RMVar_hsa_circ_320516,RMVar_hsa_circ_188561,RMVar_hsa_circ_318514,RMVar_hsa_circ_45140,RMVar_hsa_circ_369770,RMVar_hsa_circ_188567,RMVar_hsa_circ_188568,RMVar_hsa_circ_39286,RMVar_hsa_circ_53963,RMVar_hsa_circ_188571,RMVar_hsa_circ_188572,RMVar_hsa_circ_286007,RMVar_hsa_circ_42726,RMVar_hsa_circ_46880,RMVar_hsa_circ_17499,RMVar_hsa_circ_86870,RMVar_hsa_circ_188573,RMVar_hsa_circ_25488,RMVar_hsa_circ_295387,RMVar_hsa_circ_50338,RMVar_hsa_circ_51639,RMVar_hsa_circ_307581,RMVar_hsa_circ_188576,RMVar_hsa_circ_306349,RMVar_hsa_circ_64843,RMVar_hsa_circ_51534,RMVar_hsa_circ_89756,RMVar_hsa_circ_188579,RMVar_hsa_circ_188580,RMVar_hsa_circ_188578,RMVar_hsa_circ_295393,RMVar_hsa_circ_342755,RMVar_hsa_circ_331928,RMVar_hsa_circ_273825,RMVar_hsa_circ_188583,RMVar_hsa_circ_188584,RMVar_hsa_circ_188585,RMVar_hsa_circ_188582 14342 RMVar_ID_14342 Human_SNP_ID_637639040 A-to-I Human chr18 + 9950493 9950493 9950493 CCACACAGTGTTTCACTTAATGATACCGAAACAAGGAAACTAATGGAAGAGTGTAAAAGACTTCA CCACACAGTGTTTCACTTAATGATACCGAAACGAGGAAACTAATGGAAGAGTGTAAAAGACTTCA A G VAPA Ensembl:ENSG00000101558 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs762450831 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1552616,Human_RBP_ID_1879188,Human_RBP_ID_2553743,Human_RBP_ID_3561005,Human_RBP_ID_6710112,Human_RBP_ID_17913317,Human_RBP_ID_18720839,Human_RBP_ID_26814291,Human_RBP_ID_27674299 Human_Splice_Rec_1893872,Human_Splice_Rec_1893873,Human_Splice_Rec_1893888,Human_Splice_Rec_1893889,Human_Splice_Rec_1893906,Human_Splice_Rec_1893907,Human_Splice_Rec_1893914,Human_Splice_Rec_1893915,Human_Splice_Rec_1893918,Human_Splice_Rec_1893919 RMVar_hsa_circ_188632,RMVar_hsa_circ_278258,RMVar_hsa_circ_265925,RMVar_hsa_circ_26811,RMVar_hsa_circ_188636,RMVar_hsa_circ_328044,RMVar_hsa_circ_75054,RMVar_hsa_circ_65874,RMVar_hsa_circ_188639 14343 RMVar_ID_14343 Human_SNP_ID_637641478 A-to-I Human chr18 - 9958916 9958916 9958916 ATGGACAAAATAAATTTCTCAGGTAGGTAGGTACACTGGGTGTCAGCAAAATGGCAATTAATACT ATGGACAAAATAAATTTCTCAGGTAGGTAGGTGCACTGGGTGTCAGCAAAATGGCAATTAATACT T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs543129391 Functional Loss SNV dbSNP153 33..33 33 - - - 14344 RMVar_ID_14344 Human_SNP_ID_637641479 A-to-I Human chr18 - 9958916 9958916 9958916 ATGGACAAAATAAATTTCTCAGGTAGGTAGGTACACTGGGTGTCAGCAAAATGGCAATTAATACT ATGGACAAAATAAATTTCTCAGGTAGGTAGGTCCACTGGGTGTCAGCAAAATGGCAATTAATACT T G - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs543129391 Functional Loss SNV dbSNP153 33..33 33 - - - 14345 RMVar_ID_14345 Human_SNP_ID_637652748 A-to-I Human chr18 + 10005260 10005260 10005260 AGGATATGAAACTCTTGCCTGTGTGGTGTTGTAAGATGTATAATTACATCAGACTAATTAACTGG AGGATATGAAACTCTTGCCTGTGTGGTGTTGTGAGATGTATAATTACATCAGACTAATTAACTGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1188246949 Functional Loss SNV dbSNP153 33..33 33 - - - 14346 RMVar_ID_14346 Human_SNP_ID_638127015 A-to-I Human chr18 - 11841466 11841466 11841466 AATTTTTGTATTTTTAGTAAAGGCAGGGTTTCACCATTTTGGCCAGGCTGGTCTTGAACTCCTGA AATTTTTGTATTTTTAGTAAAGGCAGGGTTTCGCCATTTTGGCCAGGCTGGTCTTGAACTCCTGA T C lnc-MPPE1-8,lnc-MPPE1-8:2,CHMP1B-AS1 RNACentral:URS0000D5BE3F,RNACentral:URS0000D5B5BC,RNACentral:URS0000D5D623 lincRNA,lincRNA,lincRNA intron,intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs896007377 Functional Loss SNV dbSNP153 33..33 33 - - - 14347 RMVar_ID_14347 Human_SNP_ID_638130708 A-to-I Human chr18 - 11854750 11854725 11854750 TGAGACTGAGTTTCATCCTTGTTGCGCAGGCTAGAGTGCAATGGCGCAATCTTGGCTCACCTCAA TGAGACTGAGTTTCATCCTTGTTGCGCAGGCT_________________________CACCTCAA GAGCCAAGATTGCGCCATTGCACTCT G lnc-MPPE1-8,lnc-MPPE1-8:2,CHMP1B-AS1 RNACentral:URS0000D5BE3F,RNACentral:URS0000D5B5BC,RNACentral:URS0000D5D623 lincRNA,lincRNA,lincRNA intron,intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1260660411 Functional Loss DEL dbSNP153 33..57 33 - - - Human_RBP_ID_13247843 14348 RMVar_ID_14348 Human_SNP_ID_638130816 A-to-I Human chr18 - 11855085 11855085 11855085 AAACAACAACAACAACAACAAAAACAAAAATTAGCCAGGTGTGTTGGTGCGCATCTGTAGTCCCA AAACAACAACAACAACAACAAAAACAAAAATTTGCCAGGTGTGTTGGTGCGCATCTGTAGTCCCA T A lnc-MPPE1-8,lnc-MPPE1-8:2,CHMP1B-AS1 RNACentral:URS0000D5BE3F,RNACentral:URS0000D5B5BC,RNACentral:URS0000D5D623 lincRNA,lincRNA,lincRNA intron,intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1188703838 Functional Loss SNV dbSNP153 33..33 33 - - - 14349 RMVar_ID_14349 Human_SNP_ID_638131011 A-to-I Human chr18 - 11855756 11855756 11855756 GTTGGTCAGGCTGGTCTCGAACTTCCAACCTCAGATGATCTGCCTGCCTCGGCCTCCCAAAGTGT GTTGGTCAGGCTGGTCTCGAACTTCCAACCTCCGATGATCTGCCTGCCTCGGCCTCCCAAAGTGT T G lnc-MPPE1-8,lnc-MPPE1-8:2,CHMP1B-AS1 RNACentral:URS0000D5BE3F,RNACentral:URS0000D5B5BC,RNACentral:URS0000D5D623 lincRNA,lincRNA,lincRNA intron,intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1244813725 Functional Loss SNV dbSNP153 33..33 33 - - - 14350 RMVar_ID_14350 Human_SNP_ID_638131614 A-to-I Human chr18 - 11858038 11858038 11858038 TGAAAACTATTCTGTTAAATGCCTTTGTAATCAAACTACTGGATCTGAGAAAAAAAGTACCAACT TGAAAACTATTCTGTTAAATGCCTTTGTAATCGAACTACTGGATCTGAGAAAAAAAGTACCAACT T C lnc-MPPE1-8,lnc-MPPE1-8:2,CHMP1B-AS1,lnc-MPPE1-8:3,lnc-MPPE1-8:4 RNACentral:URS0000D5BE3F,RNACentral:URS0000D5B5BC,RNACentral:URS0000D5D623,RNACentral:URS0000D5A2D5,RNACentral:URS0000D5B93E lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,exon,exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1441731950 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2531501,Human_RBP_ID_8468153 14351 RMVar_ID_14351 Human_SNP_ID_638131615 A-to-I Human chr18 - 11858038 11858038 11858038 TGAAAACTATTCTGTTAAATGCCTTTGTAATCAAACTACTGGATCTGAGAAAAAAAGTACCAACT TGAAAACTATTCTGTTAAATGCCTTTGTAATCCAACTACTGGATCTGAGAAAAAAAGTACCAACT T G lnc-MPPE1-8,lnc-MPPE1-8:2,CHMP1B-AS1,lnc-MPPE1-8:3,lnc-MPPE1-8:4 RNACentral:URS0000D5BE3F,RNACentral:URS0000D5B5BC,RNACentral:URS0000D5D623,RNACentral:URS0000D5A2D5,RNACentral:URS0000D5B93E lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,exon,exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1441731950 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2531501,Human_RBP_ID_8468153 14352 RMVar_ID_14352 Human_SNP_ID_638137163 A-to-I Human chr18 - 11878375 11878375 11878375 ACAATCATAGCTCACTGCCACCTCAAATTCCTAGGCTCAAGGGATCCTCCCACCTCAGCCTCCTG ACAATCATAGCTCACTGCCACCTCAAATTCCTCGGCTCAAGGGATCCTCCCACCTCAGCCTCCTG T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202140940 Functional Loss SNV dbSNP153 33..33 33 - - - 14353 RMVar_ID_14353 Human_SNP_ID_638137270 A-to-I Human chr18 + 11878802 11878802 11878802 GTTGGCCAGGCTGGTCTCGAACTCCTCGCCTCAAGTGATCCTCCTGCCTCCACCTCCCAAAGTGC GTTGGCCAGGCTGGTCTCGAACTCCTCGCCTCGAGTGATCCTCCTGCCTCCACCTCCCAAAGTGC A G GNAL Ensembl:ENSG00000141404 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs973360807 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_188679,RMVar_hsa_circ_188681 14354 RMVar_ID_14354 Human_SNP_ID_638138506 A-to-I Human chr18 + 11882410 11882410 11882410 AGCAAACAGTAAGAGAAAAACAAAATGTGGCCAGGCGCGGTGGCTCACGCCTGTAATCCCAGCAC AGCAAACAGTAAGAGAAAAACAAAATGTGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCAC A G GNAL Ensembl:ENSG00000141404 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs539782959 Functional Loss SNV dbSNP153 33..33 33 - - - 14355 RMVar_ID_14355 Human_SNP_ID_638138981 A-to-I Human chr18 + 11883888 11883888 11883888 AATTTTTGTATTTCTAGCGGAGACGAGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGA AATTTTTGTATTTCTAGCGGAGACGAGGTTTCCCCATGTTGGCCAGGCTGGTCTTGAACTCCTGA A C GNAL Ensembl:ENSG00000141404 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1258483251 Functional Loss SNV dbSNP153 33..33 33 - - - 14356 RMVar_ID_14356 Human_SNP_ID_638141111 A-to-I Human chr18 - 11891422 11891422 11891422 TCACCAAGTCTGGAGTGCAGTGGCGTGATCTCAGCTTACTACAACCTCTGCCTCCCTGGTTCAAG TCACCAAGTCTGGAGTGCAGTGGCGTGATCTCGGCTTACTACAACCTCTGCCTCCCTGGTTCAAG T C MPPE1 Ensembl:ENSG00000154889 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1273647884 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1895354 14357 RMVar_ID_14357 Human_SNP_ID_638143738 A-to-I Human chr18 - 11901323 11901323 11901323 GGGAGGCTCAGGTAGGAGGATTGCTTGAGCCCAGGAGGTGGAGGTTGTAGTGAGCTGAGAGCACA GGGAGGCTCAGGTAGGAGGATTGCTTGAGCCCGGGAGGTGGAGGTTGTAGTGAGCTGAGAGCACA T C MPPE1 Ensembl:ENSG00000154889 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1050390248 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_363954 14358 RMVar_ID_14358 Human_SNP_ID_638188867 A-to-I Human chr18 + 12067424 12067424 12067424 CCAGGGCCGAGCGGGAAATTAGCCCTGCCGGCACCCGGCCCGATGGGGTTCATGATAGTGTACAT CCAGGGCCGAGCGGGAAATTAGCCCTGCCGGCGCCCGGCCCGATGGGGTTCATGATAGTGTACAT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs958504722 Functional Loss SNV dbSNP153 33..33 33 - - - 14359 RMVar_ID_14359 Human_SNP_ID_638188884 A-to-I Human chr18 + 12067463 12067463 12067463 CCGATGGGGTTCATGATAGTGTACATGTTTTCACTGGAGTTGGTAGAATCTCCAGGGCTAGGCAT CCGATGGGGTTCATGATAGTGTACATGTTTTCGCTGGAGTTGGTAGAATCTCCAGGGCTAGGCAT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1241119757 Functional Loss SNV dbSNP153 33..33 33 - - - 14360 RMVar_ID_14360 Human_SNP_ID_638188886 A-to-I Human chr18 + 12067475 12067475 12067475 ATGATAGTGTACATGTTTTCACTGGAGTTGGTAGAATCTCCAGGGCTAGGCATGATGAGGTGTTC ATGATAGTGTACATGTTTTCACTGGAGTTGGTGGAATCTCCAGGGCTAGGCATGATGAGGTGTTC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1292163960 Functional Loss SNV dbSNP153 33..33 33 - - - 14361 RMVar_ID_14361 Human_SNP_ID_638195182 A-to-I Human chr18 + 12092382 12092382 12092382 TGCAGGGGTGTGTTTCCCACAAAGGTGTGAGCATTCCCATTGGCCCGAAGCTTGGTGACCAGATG TGCAGGGGTGTGTTTCCCACAAAGGTGTGAGCTTTCCCATTGGCCCGAAGCTTGGTGACCAGATG A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251000818 Functional Loss SNV dbSNP153 33..33 33 - - - 14362 RMVar_ID_14362 Human_SNP_ID_638195189 A-to-I Human chr18 + 12092397 12092397 12092397 CCCACAAAGGTGTGAGCATTCCCATTGGCCCGAAGCTTGGTGACCAGATGGGTGACCAACCCCAG CCCACAAAGGTGTGAGCATTCCCATTGGCCCGGAGCTTGGTGACCAGATGGGTGACCAACCCCAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1382917072 Functional Loss SNV dbSNP153 33..33 33 - - - 14363 RMVar_ID_14363 Human_SNP_ID_638222729 A-to-I Human chr18 + 12212165 12212165 12212165 CAGGGGGCTGAGGCATGAGAATTCTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCCGAGATCATG CAGGGGGCTGAGGCATGAGAATTCTTGAACCCGGGAGGCAGAGGTTGCAGTGAGCCGAGATCATG A G AP005264.5 Ensembl:ENSG00000267733 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1272687041 Functional Loss SNV dbSNP153 33..33 33 - - - 14364 RMVar_ID_14364 Human_SNP_ID_638251980 A-to-I Human chr18 + 12319692 12319692 12319692 TCATTAAAGAAGAGCTGGGCTCAGGCGTTCACACCTGCCATCCCAGCACTTTGGGAGGCCAAGAC TCATTAAAGAAGAGCTGGGCTCAGGCGTTCACGCCTGCCATCCCAGCACTTTGGGAGGCCAAGAC A G TUBB6 Ensembl:ENSG00000176014 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs987604904 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3263,RMVar_hsa_circ_119049,RMVar_hsa_circ_188687,RMVar_hsa_circ_188689,RMVar_hsa_circ_115124,RMVar_hsa_circ_88568,RMVar_hsa_circ_188691 14365 RMVar_ID_14365 Human_SNP_ID_638252516 A-to-I Human chr18 + 12322136 12322136 12322136 CAGCCTGGCCAACGTGGTGAAACCCTCTCTCTACTAAAAAATACAAAAATTAGCCGGGTGTGGTG CAGCCTGGCCAACGTGGTGAAACCCTCTCTCTCCTAAAAAATACAAAAATTAGCCGGGTGTGGTG A C TUBB6 Ensembl:ENSG00000176014 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1157522328 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119049,RMVar_hsa_circ_188687,RMVar_hsa_circ_188689,RMVar_hsa_circ_115124,RMVar_hsa_circ_88568,RMVar_hsa_circ_188691 14366 RMVar_ID_14366 Human_SNP_ID_638252585 A-to-I Human chr18 + 12322413 12322413 12322413 GTCTTGCTCTGTCACCCAGGCTGGAGTGCTGTAGCACAATCTTGGCTCACTGCAACCTCCATCTT GTCTTGCTCTGTCACCCAGGCTGGAGTGCTGTGGCACAATCTTGGCTCACTGCAACCTCCATCTT A G TUBB6 Ensembl:ENSG00000176014 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1245703705 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119049,RMVar_hsa_circ_188687,RMVar_hsa_circ_188689,RMVar_hsa_circ_115124,RMVar_hsa_circ_88568,RMVar_hsa_circ_188691 14367 RMVar_ID_14367 Human_SNP_ID_638253116 A-to-I Human chr18 + 12324625 12324625 12324625 GCTCCCCACCACCACGCCCGGCTGATTTTTGTATTTTCAGTAGAGATGGGGTTTCCTCATGTTGC GCTCCCCACCACCACGCCCGGCTGATTTTTGTGTTTTCAGTAGAGATGGGGTTTCCTCATGTTGC A G TUBB6 Ensembl:ENSG00000176014 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs952489368 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119049,RMVar_hsa_circ_188687,RMVar_hsa_circ_188689,RMVar_hsa_circ_115124,RMVar_hsa_circ_88568,RMVar_hsa_circ_188691 14368 RMVar_ID_14368 Human_SNP_ID_638253137 A-to-I Human chr18 + 12324694 12324694 12324694 GCTGGTCTCTAACTCCTGACTTCAAGTGATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTAC GCTGGTCTCTAACTCCTGACTTCAAGTGATCCCCCCGCCTCGGCCTCCCAAAGTGCTGGGATTAC A C TUBB6 Ensembl:ENSG00000176014 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs887312606 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119049,RMVar_hsa_circ_188687,RMVar_hsa_circ_188689,RMVar_hsa_circ_115124,RMVar_hsa_circ_88568,RMVar_hsa_circ_188691 14369 RMVar_ID_14369 Human_SNP_ID_638255959 A-to-I Human chr18 - 12333640 12333640 12333640 AATATTTTGGCCAAGAACTGTGGCACATGTCTATAATCCCAGCACTTTGGGAGGCTGAGGTGGGT AATATTTTGGCCAAGAACTGTGGCACATGTCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGT T C AFG3L2 Ensembl:ENSG00000141385 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909786765 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78091,RMVar_hsa_circ_123567,RMVar_hsa_circ_107465,RMVar_hsa_circ_188692,RMVar_hsa_circ_188693,RMVar_hsa_circ_188694 14370 RMVar_ID_14370 Human_SNP_ID_638258616 A-to-I Human chr18 - 12344183 12344183 12344183 GAGGAGAAGAAGACTGTGGCATACCACGAAGCAGGCCATGCGGTTGCCGGCTGGTATCTGGAGCA GAGGAGAAGAAGACTGTGGCATACCACGAAGCGGGCCATGCGGTTGCCGGCTGGTATCTGGAGCA T C AFG3L2 Ensembl:ENSG00000141385 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) 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 14371 RMVar_ID_14371 Human_SNP_ID_638261729 A-to-I Human chr18 - 12355052 12355052 12355052 CACCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACTATGTTGGCCAGGCTGG CACCATGCCCAGCTAATTTTTGTATTTTTAGTGGAGATGGGGTTTCACTATGTTGGCCAGGCTGG T C AFG3L2 Ensembl:ENSG00000141385 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs76014309 Functional Loss SNV dbSNP153 33..33 33 - - - 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_344321,RMVar_hsa_circ_29644,RMVar_hsa_circ_43656,RMVar_hsa_circ_16633,RMVar_hsa_circ_946,RMVar_hsa_circ_33127,RMVar_hsa_circ_116357,RMVar_hsa_circ_343859,RMVar_hsa_circ_92799,RMVar_hsa_circ_48703,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_314548,RMVar_hsa_circ_374014,RMVar_hsa_circ_328051,RMVar_hsa_circ_348254,RMVar_hsa_circ_188700,RMVar_hsa_circ_365269,RMVar_hsa_circ_347712,RMVar_hsa_circ_39336,RMVar_hsa_circ_188706,RMVar_hsa_circ_42158,RMVar_hsa_circ_188701,RMVar_hsa_circ_188702,RMVar_hsa_circ_338507,RMVar_hsa_circ_367937,RMVar_hsa_circ_358776,RMVar_hsa_circ_301439,RMVar_hsa_circ_188705 14372 RMVar_ID_14372 Human_SNP_ID_638276957 A-to-I Human chr18 + 12410733 12410733 12410733 TTTTCCTTTTTTTTGAGGCAGAATCTTGCTCTATCACCCAGGCTGGAGTGCAGTGGCACGATCTT TTTTCCTTTTTTTTGAGGCAGAATCTTGCTCTGTCACCCAGGCTGGAGTGCAGTGGCACGATCTT A G PRELID3A Ensembl:ENSG00000141391 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1179964598 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1895790 14373 RMVar_ID_14373 Human_SNP_ID_638284971 A-to-I Human chr18 + 12439573 12439573 12439573 TGAGACGGGGTTTCGCTCTTGTTGCCTAGGCTAGAGTGCAATGGTACGATCTCAGCTCACCACAA TGAGACGGGGTTTCGCTCTTGTTGCCTAGGCTGGAGTGCAATGGTACGATCTCAGCTCACCACAA A G AP001029.2 Ensembl:ENSG00000267199 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1302439061 Functional Loss SNV dbSNP153 33..33 33 - - - 14374 RMVar_ID_14374 Human_SNP_ID_638294043 A-to-I Human chr18 - 12476494 12476494 12476494 CTCTGCCAGCCAGGCTGTAGCACAATGGCCCAATCTCTGCTCACTGCAAACTCGACCTCCCAGGT CTCTGCCAGCCAGGCTGTAGCACAATGGCCCAGTCTCTGCTCACTGCAAACTCGACCTCCCAGGT T C SPIRE1 Ensembl:ENSG00000134278 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1477880120 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5011,RMVar_hsa_circ_188722,RMVar_hsa_circ_341933,RMVar_hsa_circ_315516,RMVar_hsa_circ_278676,RMVar_hsa_circ_306695,RMVar_hsa_circ_378204,RMVar_hsa_circ_274681,RMVar_hsa_circ_34365,RMVar_hsa_circ_125506,RMVar_hsa_circ_27694,RMVar_hsa_circ_188724,RMVar_hsa_circ_188726,RMVar_hsa_circ_188728,RMVar_hsa_circ_188727,RMVar_hsa_circ_188725,RMVar_hsa_circ_30692 14375 RMVar_ID_14375 Human_SNP_ID_638295636 A-to-I Human chr18 - 12482271 12482271 12482271 GGGCGTGGTGGCACATGCCTGTAGTCCCGGCTACTCTGGAGGCTGAGGCAGGAGAATCGCTTGAA GGGCGTGGTGGCACATGCCTGTAGTCCCGGCTGCTCTGGAGGCTGAGGCAGGAGAATCGCTTGAA T C SPIRE1 Ensembl:ENSG00000134278 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1310529524 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5011,RMVar_hsa_circ_306695,RMVar_hsa_circ_378204,RMVar_hsa_circ_274681,RMVar_hsa_circ_34365,RMVar_hsa_circ_125506,RMVar_hsa_circ_27694,RMVar_hsa_circ_57843,RMVar_hsa_circ_188724,RMVar_hsa_circ_188726,RMVar_hsa_circ_188727,RMVar_hsa_circ_188725,RMVar_hsa_circ_296800,RMVar_hsa_circ_316827,RMVar_hsa_circ_30692,RMVar_hsa_circ_299184,RMVar_hsa_circ_289787,RMVar_hsa_circ_188730,RMVar_hsa_circ_188731,RMVar_hsa_circ_188732 14376 RMVar_ID_14376 Human_SNP_ID_638296810 A-to-I Human chr18 - 12487532 12487532 12487532 AAATTAGCTGGGCCTGGTGGCAGGCACCTGTAATCCCAGCTACTCGGGAGATTGCTTGAACCTGG AAATTAGCTGGGCCTGGTGGCAGGCACCTGTACTCCCAGCTACTCGGGAGATTGCTTGAACCTGG T G SPIRE1 Ensembl:ENSG00000134278 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs894804262 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11582,RMVar_hsa_circ_5011,RMVar_hsa_circ_378204,RMVar_hsa_circ_274681,RMVar_hsa_circ_34365,RMVar_hsa_circ_125506,RMVar_hsa_circ_27694,RMVar_hsa_circ_57843,RMVar_hsa_circ_188724,RMVar_hsa_circ_188726,RMVar_hsa_circ_188725,RMVar_hsa_circ_296800,RMVar_hsa_circ_316827,RMVar_hsa_circ_299184,RMVar_hsa_circ_289787,RMVar_hsa_circ_188730,RMVar_hsa_circ_188731,RMVar_hsa_circ_188732,RMVar_hsa_circ_28156,RMVar_hsa_circ_306850,RMVar_hsa_circ_188733 14377 RMVar_ID_14377 Human_SNP_ID_638302617 A-to-I Human chr18 - 12511972 12511972 12511972 AAGGCAGGAAGATTGCTGGAGCTTAGGAATTCAAGACCAGCCTGGACAACATAGTGAGACCCTAT AAGGCAGGAAGATTGCTGGAGCTTAGGAATTCGAGACCAGCCTGGACAACATAGTGAGACCCTAT T C SPIRE1 Ensembl:ENSG00000134278 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs902556429 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11582,RMVar_hsa_circ_378204,RMVar_hsa_circ_34365,RMVar_hsa_circ_125506,RMVar_hsa_circ_27694,RMVar_hsa_circ_57843,RMVar_hsa_circ_188724,RMVar_hsa_circ_188725,RMVar_hsa_circ_299184,RMVar_hsa_circ_188732,RMVar_hsa_circ_188744,RMVar_hsa_circ_188735,RMVar_hsa_circ_310369,RMVar_hsa_circ_322288,RMVar_hsa_circ_295028,RMVar_hsa_circ_39094,RMVar_hsa_circ_316016,RMVar_hsa_circ_188739,RMVar_hsa_circ_188734,RMVar_hsa_circ_329133,RMVar_hsa_circ_188740,RMVar_hsa_circ_323244,RMVar_hsa_circ_313999,RMVar_hsa_circ_283313,RMVar_hsa_circ_188742,RMVar_hsa_circ_188743 14378 RMVar_ID_14378 Human_SNP_ID_638317024 A-to-I Human chr18 - 12572413 12572413 12572413 GAGACAGGCTGGGTGTGGTGGCTCATGTCTGTAATCCTAGCACTGTGTGAGGCTGAGGCAAGAGG GAGACAGGCTGGGTGTGGTGGCTCATGTCTGTGATCCTAGCACTGTGTGAGGCTGAGGCAAGAGG T C SPIRE1 Ensembl:ENSG00000134278 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs532465486 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 14379 RMVar_ID_14379 Human_SNP_ID_638329269 A-to-I Human chr18 - 12623278 12623278 12623278 GTGGTGGCGGGCGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATGGCATGAACCTA GTGGTGGCGGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCATGAACCTA T C SPIRE1 Ensembl:ENSG00000134278 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs917067294 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 14380 RMVar_ID_14380 Human_SNP_ID_638340303 A-to-I Human chr18 + 12665791 12665791 12665791 ACAATCTCTGCTTACTGCAACCTCTGCCTCCCAGGCTCATGCAGTTCTCCTGCCTCAGCCTCCCG ACAATCTCTGCTTACTGCAACCTCTGCCTCCCGGGCTCATGCAGTTCTCCTGCCTCAGCCTCCCG A G PSMG2 Ensembl:ENSG00000128789 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027081379 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78226,RMVar_hsa_circ_188748 14381 RMVar_ID_14381 Human_SNP_ID_638340304 A-to-I Human chr18 + 12665797 12665797 12665797 TCTGCTTACTGCAACCTCTGCCTCCCAGGCTCATGCAGTTCTCCTGCCTCAGCCTCCCGAGTAGC TCTGCTTACTGCAACCTCTGCCTCCCAGGCTCGTGCAGTTCTCCTGCCTCAGCCTCCCGAGTAGC A G PSMG2 Ensembl:ENSG00000128789 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560807122 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78226,RMVar_hsa_circ_188748 14382 RMVar_ID_14382 Human_SNP_ID_638340305 A-to-I Human chr18 + 12665797 12665797 12665797 TCTGCTTACTGCAACCTCTGCCTCCCAGGCTCATGCAGTTCTCCTGCCTCAGCCTCCCGAGTAGC TCTGCTTACTGCAACCTCTGCCTCCCAGGCTCTTGCAGTTCTCCTGCCTCAGCCTCCCGAGTAGC A T PSMG2 Ensembl:ENSG00000128789 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560807122 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78226,RMVar_hsa_circ_188748 14383 RMVar_ID_14383 Human_SNP_ID_638341639 A-to-I Human chr18 - 12670244 12670226 12670245 CTCACTGCAACCTCCACCTCGCAGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCCAAGTAGCTGGG CTCACTGCAACCTCCACCTCGCAGGTTCAAG___________________TCCCAAGTAGCTGGG AGGCTGAGGCAGGAGAACTG A CEP76 Ensembl:ENSG00000101624 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1467462412 Functional Loss DEL dbSNP153 32..50 33 - - - 14384 RMVar_ID_14384 Human_SNP_ID_638341822 A-to-I Human chr18 - 12670924 12670924 12670924 AAGCTTTTTTTAAAGCATAGTGGTTCACACCTATAATTCCAGTACTCTGGGAGGCTGAGGCAGGA AAGCTTTTTTTAAAGCATAGTGGTTCACACCTGTAATTCCAGTACTCTGGGAGGCTGAGGCAGGA T C CEP76,AP005482.4 Ensembl:ENSG00000101624,Ensembl:ENSG00000267249 Protein coding,lincRNA intron,exon GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs908976758 Functional Loss SNV dbSNP153 33..33 33 - - - 14385 RMVar_ID_14385 Human_SNP_ID_638342170 A-to-I Human chr18 - 12671976 12671976 12671976 GTCTCTACTAAAGATACAAAAATTAGCTGGGCATGGTGGCATGTGCCTGTAGTCTAGCTACTCAG GTCTCTACTAAAGATACAAAAATTAGCTGGGCGTGGTGGCATGTGCCTGTAGTCTAGCTACTCAG T C CEP76 Ensembl:ENSG00000101624 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910348775 Functional Loss SNV dbSNP153 33..33 33 - - - 14386 RMVar_ID_14386 Human_SNP_ID_638345003 A-to-I Human chr18 - 12682760 12682760 12682760 AAAATTAGCTGGGTGTGGTGGTGCACGCCTGTAGTCCTAGCTACTCAGGAGGCTGAGAATCATTG AAAATTAGCTGGGTGTGGTGGTGCACGCCTGTGGTCCTAGCTACTCAGGAGGCTGAGAATCATTG T C CEP76 Ensembl:ENSG00000101624 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1252341307 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59373,RMVar_hsa_circ_378695,RMVar_hsa_circ_52571,RMVar_hsa_circ_188750,RMVar_hsa_circ_11379,RMVar_hsa_circ_52957,RMVar_hsa_circ_188752,RMVar_hsa_circ_370461,RMVar_hsa_circ_344327,RMVar_hsa_circ_188753 14387 RMVar_ID_14387 Human_SNP_ID_638347566 A-to-I Human chr18 - 12692297 12692297 12692297 TTTTTTTTTTTTTTGAGATAGAGTCTCACTCTATCGCCCAGGGTGGAGCACGGTGGCATGAACTC TTTTTTTTTTTTTTGAGATAGAGTCTCACTCTGTCGCCCAGGGTGGAGCACGGTGGCATGAACTC T C CEP76 Ensembl:ENSG00000101624 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs888669428 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1896228 RMVar_hsa_circ_378695,RMVar_hsa_circ_126986,RMVar_hsa_circ_188750,RMVar_hsa_circ_11379,RMVar_hsa_circ_188752,RMVar_hsa_circ_370461,RMVar_hsa_circ_188753,RMVar_hsa_circ_353130,RMVar_hsa_circ_188754,RMVar_hsa_circ_49960 14388 RMVar_ID_14388 Human_SNP_ID_638348001 A-to-I Human chr18 - 12693952 12693952 12693952 TGGTACATACTTGTAGTCCCAGCTGCTTGGGAAGCTGAAATGGGAGGATTGCTTGACCCAGGAAT TGGTACATACTTGTAGTCCCAGCTGCTTGGGAGGCTGAAATGGGAGGATTGCTTGACCCAGGAAT T C CEP76 Ensembl:ENSG00000101624 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1234800665 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_378695,RMVar_hsa_circ_126986,RMVar_hsa_circ_188750,RMVar_hsa_circ_11379,RMVar_hsa_circ_188752,RMVar_hsa_circ_370461,RMVar_hsa_circ_188753,RMVar_hsa_circ_353130,RMVar_hsa_circ_188754,RMVar_hsa_circ_49960 14389 RMVar_ID_14389 Human_SNP_ID_638356717 A-to-I Human chr18 - 12724845 12724845 12724845 CTAACATGAATAGTAAGTACAATGAAGAACTAAGGATTTTCCTTTTTGGAAAGTCAGCTTTAATG CTAACATGAATAGTAAGTACAATGAAGAACTAGGGATTTTCCTTTTTGGAAAGTCAGCTTTAATG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285212544 Functional Loss SNV dbSNP153 33..33 33 - - - 14390 RMVar_ID_14390 Human_SNP_ID_638375720 A-to-I Human chr18 - 12792415 12792415 12792415 ATCTGGGCGTGGTGGTGCATGCCTGTAGTCCCAGCTCCTTGGGAGGCTAAGGCAGGAGAATCACT ATCTGGGCGTGGTGGTGCATGCCTGTAGTCCCCGCTCCTTGGGAGGCTAAGGCAGGAGAATCACT T G PTPN2 Ensembl:ENSG00000175354 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs747063409 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_188763 14391 RMVar_ID_14391 Human_SNP_ID_638396098 A-to-I Human chr18 - 12870581 12870581 12870581 TGGTGTAAACCTGGGAGGTGGAGCTTGCAGTAAGCCAAGATCGCGCCACTGCACTCCAGCCTGGG TGGTGTAAACCTGGGAGGTGGAGCTTGCAGTAGGCCAAGATCGCGCCACTGCACTCCAGCCTGGG T C PTPN2 Ensembl:ENSG00000175354 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1224322527 Functional Loss SNV dbSNP153 33..33 33 - - - 14392 RMVar_ID_14392 Human_SNP_ID_638396099 A-to-I Human chr18 - 12870582 12870582 12870582 ATGGTGTAAACCTGGGAGGTGGAGCTTGCAGTAAGCCAAGATCGCGCCACTGCACTCCAGCCTGG ATGGTGTAAACCTGGGAGGTGGAGCTTGCAGTTAGCCAAGATCGCGCCACTGCACTCCAGCCTGG T A PTPN2 Ensembl:ENSG00000175354 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs541551803 Functional Loss SNV dbSNP153 33..33 33 - - - 14393 RMVar_ID_14393 Human_SNP_ID_638396100 A-to-I Human chr18 - 12870582 12870582 12870582 ATGGTGTAAACCTGGGAGGTGGAGCTTGCAGTAAGCCAAGATCGCGCCACTGCACTCCAGCCTGG ATGGTGTAAACCTGGGAGGTGGAGCTTGCAGTGAGCCAAGATCGCGCCACTGCACTCCAGCCTGG T C PTPN2 Ensembl:ENSG00000175354 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs541551803 Functional Loss SNV dbSNP153 33..33 33 - - - 14394 RMVar_ID_14394 Human_SNP_ID_638396148 A-to-I Human chr18 - 12870704 12870704 12870704 GAGATCGAGACCATCCTGGCTAACACGGTGAAACCCCGTCTCTACTAAAAACACAAAAAAAGTAG GAGATCGAGACCATCCTGGCTAACACGGTGAATCCCCGTCTCTACTAAAAACACAAAAAAAGTAG T A PTPN2 Ensembl:ENSG00000175354 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1351127626 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_136613 14395 RMVar_ID_14395 Human_SNP_ID_638396154 A-to-I Human chr18 - 12870712 12870712 12870712 GAGGTCAGGAGATCGAGACCATCCTGGCTAACACGGTGAAACCCCGTCTCTACTAAAAACACAAA GAGGTCAGGAGATCGAGACCATCCTGGCTAACGCGGTGAAACCCCGTCTCTACTAAAAACACAAA T C PTPN2 Ensembl:ENSG00000175354 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1474864757 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_136613 14396 RMVar_ID_14396 Human_SNP_ID_638396508 A-to-I Human chr18 - 12872004 12872004 12872004 TGCTCTGTGGCCCCAGGCTGGAATGCTACGGCACGATCTCGGCTTACTGCAACCTCTGCATGCTG TGCTCTGTGGCCCCAGGCTGGAATGCTACGGCGCGATCTCGGCTTACTGCAACCTCTGCATGCTG T C PTPN2 Ensembl:ENSG00000175354 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs939748140 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13250018 14397 RMVar_ID_14397 Human_SNP_ID_638396509 A-to-I Human chr18 - 12872004 12872004 12872004 TGCTCTGTGGCCCCAGGCTGGAATGCTACGGCACGATCTCGGCTTACTGCAACCTCTGCATGCTG TGCTCTGTGGCCCCAGGCTGGAATGCTACGGCCCGATCTCGGCTTACTGCAACCTCTGCATGCTG T G PTPN2 Ensembl:ENSG00000175354 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs939748140 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13250018 14398 RMVar_ID_14398 Human_SNP_ID_638396803 A-to-I Human chr18 - 12872964 12872964 12872964 CACCCACCTTGGCCTCCCAAATTGCTGGGATTACAGGCGTGAGCCACCGCGTCCAGCCTGTTACA CACCCACCTTGGCCTCCCAAATTGCTGGGATTGCAGGCGTGAGCCACCGCGTCCAGCCTGTTACA T C PTPN2 Ensembl:ENSG00000175354 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs915244081 Functional Loss SNV dbSNP153 33..33 33 - - - 14399 RMVar_ID_14399 Human_SNP_ID_638408493 A-to-I Human chr18 + 12912898 12912898 12912898 AGAGAACATGGCGGCCCAGAGGGAATGGACCCAGATGGTGTCATCTAGAGCAACTGGGATGAGAT AGAGAACATGGCGGCCCAGAGGGAATGGACCCGGATGGTGTCATCTAGAGCAACTGGGATGAGAT A G EIF4A2P1 Ensembl:ENSG00000267336 Pseudogene exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1289320792 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17381928 Human_miRNA_ID_1872310 14400 RMVar_ID_14400 Human_SNP_ID_638422107 A-to-I Human chr18 + 12966442 12966442 12966442 TTTTTTATGTATTTGTTTTCGAGACACGTGTCACTATGTCACCCAGGCTGGAGTGCAGTGGCACT TTTTTTATGTATTTGTTTTCGAGACACGTGTCTCTATGTCACCCAGGCTGGAGTGCAGTGGCACT A T SEH1L Ensembl:ENSG00000085415 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs890703552 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6668554,Human_RBP_ID_13250311 RMVar_hsa_circ_21712,RMVar_hsa_circ_309226,RMVar_hsa_circ_94980,RMVar_hsa_circ_188776,RMVar_hsa_circ_69614,RMVar_hsa_circ_188773,RMVar_hsa_circ_188774,RMVar_hsa_circ_78848,RMVar_hsa_circ_119598,RMVar_hsa_circ_373002,RMVar_hsa_circ_346102,RMVar_hsa_circ_188778,RMVar_hsa_circ_188779,RMVar_hsa_circ_188777 14401 RMVar_ID_14401 Human_SNP_ID_638423070 A-to-I Human chr18 + 12970469 12970469 12970469 CTGAAAGAGACTCTCACTCTGTTGCCCAGGCTAGAGTGCAGTGGCACGATCATAGCTCACTGCAG CTGAAAGAGACTCTCACTCTGTTGCCCAGGCTGGAGTGCAGTGGCACGATCATAGCTCACTGCAG A G SEH1L Ensembl:ENSG00000085415 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1359133970 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21712,RMVar_hsa_circ_309226,RMVar_hsa_circ_94980,RMVar_hsa_circ_188776,RMVar_hsa_circ_69614,RMVar_hsa_circ_188773,RMVar_hsa_circ_188774,RMVar_hsa_circ_78848,RMVar_hsa_circ_119598,RMVar_hsa_circ_373002,RMVar_hsa_circ_346102,RMVar_hsa_circ_188778,RMVar_hsa_circ_188779,RMVar_hsa_circ_188777 14402 RMVar_ID_14402 Human_SNP_ID_638423686 A-to-I Human chr18 + 12972959 12972959 12972959 CACGCGAGGTGACTTATGCCTGCCATCTCAGCACTTTGGGAGGCTGAGGTGGGTGGATCACTTGA CACGCGAGGTGACTTATGCCTGCCATCTCAGCGCTTTGGGAGGCTGAGGTGGGTGGATCACTTGA A G SEH1L Ensembl:ENSG00000085415 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1487453972 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21712,RMVar_hsa_circ_94980,RMVar_hsa_circ_188776,RMVar_hsa_circ_69614,RMVar_hsa_circ_188774,RMVar_hsa_circ_78848,RMVar_hsa_circ_119598,RMVar_hsa_circ_373002,RMVar_hsa_circ_188778,RMVar_hsa_circ_188777,RMVar_hsa_circ_35341,RMVar_hsa_circ_82701,RMVar_hsa_circ_345545,RMVar_hsa_circ_188781,RMVar_hsa_circ_188782,RMVar_hsa_circ_188783 14403 RMVar_ID_14403 Human_SNP_ID_638423702 A-to-I Human chr18 + 12973053 12973053 12973053 CATGGTGAAACCCTTTCGCTACAAAAAGTACAAAAATTAGCTGTGGGGATGATGGCGCATGCCTG CATGGTGAAACCCTTTCGCTACAAAAAGTACAGAAATTAGCTGTGGGGATGATGGCGCATGCCTG A G SEH1L Ensembl:ENSG00000085415 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs924102476 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21712,RMVar_hsa_circ_94980,RMVar_hsa_circ_188776,RMVar_hsa_circ_69614,RMVar_hsa_circ_188774,RMVar_hsa_circ_78848,RMVar_hsa_circ_119598,RMVar_hsa_circ_373002,RMVar_hsa_circ_188778,RMVar_hsa_circ_188777,RMVar_hsa_circ_35341,RMVar_hsa_circ_82701,RMVar_hsa_circ_345545,RMVar_hsa_circ_188781,RMVar_hsa_circ_188782,RMVar_hsa_circ_188783 14404 RMVar_ID_14404 Human_SNP_ID_638423769 A-to-I Human chr18 + 12973369 12973369 12973369 TCACCCAAGCTGGAGTGCAGTGATGCAATCTCAGCTCACTGCAACCTCTACCTCCCGAGTTCAAG TCACCCAAGCTGGAGTGCAGTGATGCAATCTCCGCTCACTGCAACCTCTACCTCCCGAGTTCAAG A C SEH1L Ensembl:ENSG00000085415 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs536388665 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21712,RMVar_hsa_circ_94980,RMVar_hsa_circ_188776,RMVar_hsa_circ_69614,RMVar_hsa_circ_188774,RMVar_hsa_circ_78848,RMVar_hsa_circ_119598,RMVar_hsa_circ_373002,RMVar_hsa_circ_188778,RMVar_hsa_circ_188777,RMVar_hsa_circ_35341,RMVar_hsa_circ_82701,RMVar_hsa_circ_345545,RMVar_hsa_circ_188781,RMVar_hsa_circ_188782,RMVar_hsa_circ_188783 14405 RMVar_ID_14405 Human_SNP_ID_638431194 A-to-I Human chr18 + 13000192 13000192 13000192 GTTAGCTAGGCTATTCTTGAACTCTTGGGCTCAAGTGATCCTCCTGCCTCAACTTCCCAAAGTGT GTTAGCTAGGCTATTCTTGAACTCTTGGGCTCGAGTGATCCTCCTGCCTCAACTTCCCAAAGTGT A G CEP192 Ensembl:ENSG00000101639 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1198787709 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_329486,RMVar_hsa_circ_350289,RMVar_hsa_circ_367260,RMVar_hsa_circ_369812,RMVar_hsa_circ_372638,RMVar_hsa_circ_367397,RMVar_hsa_circ_357461,RMVar_hsa_circ_364963,RMVar_hsa_circ_351343,RMVar_hsa_circ_345343,RMVar_hsa_circ_349667,RMVar_hsa_circ_331337,RMVar_hsa_circ_317853,RMVar_hsa_circ_321898,RMVar_hsa_circ_323198,RMVar_hsa_circ_319510,RMVar_hsa_circ_310902,RMVar_hsa_circ_311622,RMVar_hsa_circ_307329,RMVar_hsa_circ_37529,RMVar_hsa_circ_274052,RMVar_hsa_circ_278556,RMVar_hsa_circ_293913,RMVar_hsa_circ_294334,RMVar_hsa_circ_286573,RMVar_hsa_circ_277042,RMVar_hsa_circ_277196,RMVar_hsa_circ_274947,RMVar_hsa_circ_53762,RMVar_hsa_circ_114353,RMVar_hsa_circ_270538,RMVar_hsa_circ_64377,RMVar_hsa_circ_50581,RMVar_hsa_circ_52577,RMVar_hsa_circ_45279,RMVar_hsa_circ_188788,RMVar_hsa_circ_188796,RMVar_hsa_circ_188800,RMVar_hsa_circ_188804,RMVar_hsa_circ_29463,RMVar_hsa_circ_35218,RMVar_hsa_circ_16354,RMVar_hsa_circ_188802,RMVar_hsa_circ_188803,RMVar_hsa_circ_188801,RMVar_hsa_circ_188798,RMVar_hsa_circ_188799,RMVar_hsa_circ_188797,RMVar_hsa_circ_188792,RMVar_hsa_circ_188794,RMVar_hsa_circ_188795,RMVar_hsa_circ_188793,RMVar_hsa_circ_188790,RMVar_hsa_circ_188791,RMVar_hsa_circ_188789,RMVar_hsa_circ_188786,RMVar_hsa_circ_188787,RMVar_hsa_circ_188785,RMVar_hsa_circ_188806 14406 RMVar_ID_14406 Human_SNP_ID_638450060 A-to-I Human chr18 + 13076815 13076815 13076815 TTATTTATTTATTTATTTTGAGACATCATCTCACTCTGTCGCCCAGCCTGGAGTGCAGTGGCGTG TTATTTATTTATTTATTTTGAGACATCATCTCCCTCTGTCGCCCAGCCTGGAGTGCAGTGGCGTG A C CEP192 Ensembl:ENSG00000101639 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1331033871 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13252195 RMVar_hsa_circ_369812,RMVar_hsa_circ_357461,RMVar_hsa_circ_345343,RMVar_hsa_circ_321898,RMVar_hsa_circ_323198,RMVar_hsa_circ_319510,RMVar_hsa_circ_310902,RMVar_hsa_circ_37529,RMVar_hsa_circ_274052,RMVar_hsa_circ_270538,RMVar_hsa_circ_29463,RMVar_hsa_circ_35218,RMVar_hsa_circ_188792,RMVar_hsa_circ_188794,RMVar_hsa_circ_188793,RMVar_hsa_circ_188790,RMVar_hsa_circ_188791,RMVar_hsa_circ_37771,RMVar_hsa_circ_94879,RMVar_hsa_circ_188811,RMVar_hsa_circ_51842,RMVar_hsa_circ_30920,RMVar_hsa_circ_188824,RMVar_hsa_circ_118359,RMVar_hsa_circ_334497,RMVar_hsa_circ_349383,RMVar_hsa_circ_26020,RMVar_hsa_circ_188828,RMVar_hsa_circ_9134,RMVar_hsa_circ_127705,RMVar_hsa_circ_102490,RMVar_hsa_circ_188837,RMVar_hsa_circ_326097,RMVar_hsa_circ_188838,RMVar_hsa_circ_321803,RMVar_hsa_circ_271826,RMVar_hsa_circ_188840,RMVar_hsa_circ_188839,RMVar_hsa_circ_45170,RMVar_hsa_circ_108167,RMVar_hsa_circ_69074,RMVar_hsa_circ_42340,RMVar_hsa_circ_188844,RMVar_hsa_circ_188843,RMVar_hsa_circ_276952,RMVar_hsa_circ_297152,RMVar_hsa_circ_188845,RMVar_hsa_circ_332055,RMVar_hsa_circ_53493,RMVar_hsa_circ_188846,RMVar_hsa_circ_188847 14407 RMVar_ID_14407 Human_SNP_ID_638460463 A-to-I Human chr18 + 13117077 13117076 13117078 GACTCCATCTCTACCAAAAAAAAAAAAAAATTAACCGGGCATGGTGGCAGGTACCTGTAGTTCCA GACTCCATCTCTACCAAAAAAAAAAAAAAATT__CCGGGCATGGTGGCAGGTACCTGTAGTTCCA TAA T CEP192 Ensembl:ENSG00000101639 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1425128490 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_274052,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_339953,RMVar_hsa_circ_188859,RMVar_hsa_circ_316081 14408 RMVar_ID_14408 Human_SNP_ID_638460473 A-to-I Human chr18 + 13117113 13117113 13117113 GGGCATGGTGGCAGGTACCTGTAGTTCCAGCTACTTGTGGGGGCTGAGCTGAGAGGATCGCTTTA GGGCATGGTGGCAGGTACCTGTAGTTCCAGCTGCTTGTGGGGGCTGAGCTGAGAGGATCGCTTTA A G CEP192 Ensembl:ENSG00000101639 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1030268647 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8468638 RMVar_hsa_circ_274052,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_339953,RMVar_hsa_circ_188859,RMVar_hsa_circ_316081 14409 RMVar_ID_14409 Human_SNP_ID_638545022 A-to-I Human chr18 + 13459138 13459138 13459138 GGCCAGGAGTTCGAAACCAGCTTGGGCAACATAGTGAGACTCCATCTCTACACCAAAAAAAAAAA GGCCAGGAGTTCGAAACCAGCTTGGGCAACATGGTGAGACTCCATCTCTACACCAAAAAAAAAAA A G LDLRAD4 Ensembl:ENSG00000168675 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1156825228 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_349072,RMVar_hsa_circ_17066,RMVar_hsa_circ_188861,RMVar_hsa_circ_188872,RMVar_hsa_circ_188877,RMVar_hsa_circ_188878,RMVar_hsa_circ_188879,RMVar_hsa_circ_188876 14410 RMVar_ID_14410 Human_SNP_ID_638560711 A-to-I Human chr18 + 13520666 13520666 13520666 CTTGAGCCCAGGAGTTCAAGACAAGCCTGGGCAACATAGGGAGACCTCGTCTCTACTAAAAATTA CTTGAGCCCAGGAGTTCAAGACAAGCCTGGGCGACATAGGGAGACCTCGTCTCTACTAAAAATTA A G LDLRAD4 Ensembl:ENSG00000168675 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs992864321 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_349072,RMVar_hsa_circ_17066,RMVar_hsa_circ_188861 14411 RMVar_ID_14411 Human_SNP_ID_638560724 A-to-I Human chr18 + 13520706 13520706 13520706 GAGACCTCGTCTCTACTAAAAATTAAAAAATTAGCTGGGCATGGTGGCAGGTGTCTGTGGTCCTA GAGACCTCGTCTCTACTAAAAATTAAAAAATTTGCTGGGCATGGTGGCAGGTGTCTGTGGTCCTA A T LDLRAD4 Ensembl:ENSG00000168675 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1316957724 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_349072,RMVar_hsa_circ_17066,RMVar_hsa_circ_188861 14412 RMVar_ID_14412 Human_SNP_ID_638600648 A-to-I Human chr18 - 13681932 13681932 13681932 ATACAATGCTGAATCCAAAGTGGTTTTGGTACAAGGCCCTCAAAAACAATGGTTGCATTTATCTG ATACAATGCTGAATCCAAAGTGGTTTTGGTACCAGGCCCTCAAAAACAATGGTTGCATTTATCTG T G FAM210A Ensembl:ENSG00000177150 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_27264125 RMVar_hsa_circ_188882,RMVar_hsa_circ_110704,RMVar_hsa_circ_188884,RMVar_hsa_circ_188883,RMVar_hsa_circ_289999,RMVar_hsa_circ_188890,RMVar_hsa_circ_52044,RMVar_hsa_circ_188889,RMVar_hsa_circ_188892,RMVar_hsa_circ_330025,RMVar_hsa_circ_291048,RMVar_hsa_circ_188891 14413 RMVar_ID_14413 Human_SNP_ID_638617969 A-to-I Human chr18 + 13749766 13749766 13749766 AGTTGGGGAGACAGAGTCTCGCTCTGTCATCCAAGCTGGAGTGCACTGACACCATCTTGGCATCT AGTTGGGGAGACAGAGTCTCGCTCTGTCATCCGAGCTGGAGTGCACTGACACCATCTTGGCATCT A G RNMT Ensembl:ENSG00000101654 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1055448445 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238538,Human_RBP_ID_13253751 RMVar_hsa_circ_278262,RMVar_hsa_circ_308445,RMVar_hsa_circ_36272,RMVar_hsa_circ_106350,RMVar_hsa_circ_188895,RMVar_hsa_circ_188896,RMVar_hsa_circ_188894,RMVar_hsa_circ_188901,RMVar_hsa_circ_331533,RMVar_hsa_circ_33646,RMVar_hsa_circ_325272,RMVar_hsa_circ_188904,RMVar_hsa_circ_188905,RMVar_hsa_circ_97734,RMVar_hsa_circ_188906 14414 RMVar_ID_14414 Human_SNP_ID_40727662 A-to-I Human chr1 + 180001511 180001511 180001511 AAACTCTTGGCCTCAAGTGATCCACTCGCCTCAGCCTCCCAAAGTGCTGGGATTCCAGGTATAAG AAACTCTTGGCCTCAAGTGATCCACTCGCCTCGGCCTCCCAAAGTGCTGGGATTCCAGGTATAAG A G CEP350 Ensembl:ENSG00000135837 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1280294284 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29021,RMVar_hsa_circ_23199,RMVar_hsa_circ_71260,RMVar_hsa_circ_329339,RMVar_hsa_circ_367526,RMVar_hsa_circ_357596,RMVar_hsa_circ_277029,RMVar_hsa_circ_288451,RMVar_hsa_circ_51686,RMVar_hsa_circ_61761,RMVar_hsa_circ_51015,RMVar_hsa_circ_12418,RMVar_hsa_circ_138029,RMVar_hsa_circ_138028,RMVar_hsa_circ_292852,RMVar_hsa_circ_362466,RMVar_hsa_circ_109842,RMVar_hsa_circ_112064,RMVar_hsa_circ_138034,RMVar_hsa_circ_138035,RMVar_hsa_circ_364523,RMVar_hsa_circ_314568,RMVar_hsa_circ_295368,RMVar_hsa_circ_111796,RMVar_hsa_circ_70766,RMVar_hsa_circ_102609,RMVar_hsa_circ_138040,RMVar_hsa_circ_138041,RMVar_hsa_circ_138042,RMVar_hsa_circ_138039,RMVar_hsa_circ_107037,RMVar_hsa_circ_96106,RMVar_hsa_circ_138043,RMVar_hsa_circ_138044,RMVar_hsa_circ_101202,RMVar_hsa_circ_138047,RMVar_hsa_circ_138048 14415 RMVar_ID_14415 Human_SNP_ID_40727664 A-to-I Human chr1 + 180001520 180001520 180001520 GCCTCAAGTGATCCACTCGCCTCAGCCTCCCAAAGTGCTGGGATTCCAGGTATAAGCCACCGTGC GCCTCAAGTGATCCACTCGCCTCAGCCTCCCAGAGTGCTGGGATTCCAGGTATAAGCCACCGTGC A G CEP350 Ensembl:ENSG00000135837 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1329669282 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29021,RMVar_hsa_circ_23199,RMVar_hsa_circ_71260,RMVar_hsa_circ_329339,RMVar_hsa_circ_367526,RMVar_hsa_circ_357596,RMVar_hsa_circ_277029,RMVar_hsa_circ_288451,RMVar_hsa_circ_51686,RMVar_hsa_circ_61761,RMVar_hsa_circ_51015,RMVar_hsa_circ_12418,RMVar_hsa_circ_138029,RMVar_hsa_circ_138028,RMVar_hsa_circ_292852,RMVar_hsa_circ_362466,RMVar_hsa_circ_109842,RMVar_hsa_circ_112064,RMVar_hsa_circ_138034,RMVar_hsa_circ_138035,RMVar_hsa_circ_364523,RMVar_hsa_circ_314568,RMVar_hsa_circ_295368,RMVar_hsa_circ_111796,RMVar_hsa_circ_70766,RMVar_hsa_circ_102609,RMVar_hsa_circ_138040,RMVar_hsa_circ_138041,RMVar_hsa_circ_138042,RMVar_hsa_circ_138039,RMVar_hsa_circ_107037,RMVar_hsa_circ_96106,RMVar_hsa_circ_138043,RMVar_hsa_circ_138044,RMVar_hsa_circ_101202,RMVar_hsa_circ_138047,RMVar_hsa_circ_138048 14416 RMVar_ID_14416 Human_SNP_ID_40741268 A-to-I Human chr1 + 180056586 180056586 180056586 CTGCCTCTAGGGCTCAAGCAATCCTCTCACCTAAGCCTCCCCTGTAGCTGGGACCACAGGTGTGC CTGCCTCTAGGGCTCAAGCAATCCTCTCACCTGAGCCTCCCCTGTAGCTGGGACCACAGGTGTGC A G CEP350 Ensembl:ENSG00000135837 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs564600224 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18429041 RMVar_hsa_circ_102609,RMVar_hsa_circ_96106,RMVar_hsa_circ_138043,RMVar_hsa_circ_138048,RMVar_hsa_circ_375793,RMVar_hsa_circ_138053,RMVar_hsa_circ_39024,RMVar_hsa_circ_69020,RMVar_hsa_circ_286173,RMVar_hsa_circ_27610,RMVar_hsa_circ_70119,RMVar_hsa_circ_69393,RMVar_hsa_circ_39953,RMVar_hsa_circ_138066,RMVar_hsa_circ_104337,RMVar_hsa_circ_21168,RMVar_hsa_circ_282211,RMVar_hsa_circ_343513,RMVar_hsa_circ_74973,RMVar_hsa_circ_138072,RMVar_hsa_circ_138073 14417 RMVar_ID_14417 Human_SNP_ID_40749951 A-to-I Human chr1 + 180094167 180094167 180094167 TTTCCATCGCTGCAGAAGATGACACTTTAGACAATACCTTTTCCGAAGAATTGGAGAAGCAACAG TTTCCATCGCTGCAGAAGATGACACTTTAGACGATACCTTTTCCGAAGAATTGGAGAAGCAACAG A G CEP350 Ensembl:ENSG00000135837 Protein coding CDS GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs768293091 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24886,Human_RBP_ID_4011036 RMVar_hsa_circ_366645,RMVar_hsa_circ_138077,RMVar_hsa_circ_275200,RMVar_hsa_circ_358702,RMVar_hsa_circ_138080,RMVar_hsa_circ_138081,RMVar_hsa_circ_311402,RMVar_hsa_circ_68105 14418 RMVar_ID_14418 Human_SNP_ID_40825146 A-to-I Human chr1 - 180401612 180401612 180401612 CCCCACTAATTTTTTGTATTTCTAGTAGAGACAGCATTTCACCATGTTGGCCAGGCTTGTTGCGA CCCCACTAATTTTTTGTATTTCTAGTAGAGACGGCATTTCACCATGTTGGCCAGGCTTGTTGCGA T C ACBD6 Ensembl:ENSG00000230124 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs967025320 Functional Loss SNV dbSNP153 33..33 33 - - - 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 14419 RMVar_ID_14419 Human_SNP_ID_40846160 A-to-I Human chr1 - 180490917 180490917 180490917 GTCTCACTCTATCACTCAGACTGGAGCACAGTAGTAGGATCTTGGCTCAACGTAACCTCCACCTC GTCTCACTCTATCACTCAGACTGGAGCACAGTGGTAGGATCTTGGCTCAACGTAACCTCCACCTC T C ACBD6 Ensembl:ENSG00000230124 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1426966337 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10683794 RMVar_hsa_circ_87926,RMVar_hsa_circ_138097,RMVar_hsa_circ_26540,RMVar_hsa_circ_90937,RMVar_hsa_circ_377578,RMVar_hsa_circ_138098,RMVar_hsa_circ_298940,RMVar_hsa_circ_138102,RMVar_hsa_circ_138103,RMVar_hsa_circ_3476,RMVar_hsa_circ_368429 14420 RMVar_ID_14420 Human_SNP_ID_40846161 A-to-I Human chr1 - 180490917 180490917 180490917 GTCTCACTCTATCACTCAGACTGGAGCACAGTAGTAGGATCTTGGCTCAACGTAACCTCCACCTC GTCTCACTCTATCACTCAGACTGGAGCACAGTCGTAGGATCTTGGCTCAACGTAACCTCCACCTC T G ACBD6 Ensembl:ENSG00000230124 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1426966337 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10683794 RMVar_hsa_circ_87926,RMVar_hsa_circ_138097,RMVar_hsa_circ_26540,RMVar_hsa_circ_90937,RMVar_hsa_circ_377578,RMVar_hsa_circ_138098,RMVar_hsa_circ_298940,RMVar_hsa_circ_138102,RMVar_hsa_circ_138103,RMVar_hsa_circ_3476,RMVar_hsa_circ_368429 14421 RMVar_ID_14421 Human_SNP_ID_40929320 A-to-I Human chr1 + 180826882 180826882 180826882 TTTCTATTAAGAAAAACTGTAGAACCAGGTGCAGTGGCTCACGCCTGTCGTCCCAGCACTTTGGG TTTCTATTAAGAAAAACTGTAGAACCAGGTGCGGTGGCTCACGCCTGTCGTCCCAGCACTTTGGG A G XPR1 Ensembl:ENSG00000143324 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs993100534 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10685075 RMVar_hsa_circ_114053,RMVar_hsa_circ_374165,RMVar_hsa_circ_58988,RMVar_hsa_circ_138107,RMVar_hsa_circ_138108,RMVar_hsa_circ_334887,RMVar_hsa_circ_88475,RMVar_hsa_circ_138116,RMVar_hsa_circ_122209,RMVar_hsa_circ_138117,RMVar_hsa_circ_138122,RMVar_hsa_circ_293994,RMVar_hsa_circ_326965,RMVar_hsa_circ_353973,RMVar_hsa_circ_124925,RMVar_hsa_circ_138123,RMVar_hsa_circ_138120,RMVar_hsa_circ_138121 14422 RMVar_ID_14422 Human_SNP_ID_40974765 A-to-I Human chr1 - 181013457 181013457 181013457 AAAATTAGCTTGGCGTGGTAGTGTGCACCTGTAGTCCTAGCAACTTGGGAGGCTGAGACGGAAGA AAAATTAGCTTGGCGTGGTAGTGTGCACCTGTGGTCCTAGCAACTTGGGAGGCTGAGACGGAAGA T C STX6 Ensembl:ENSG00000135823 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1008937237 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_138134,RMVar_hsa_circ_101653 14423 RMVar_ID_14423 Human_SNP_ID_41024361 A-to-I Human chr1 + 181215125 181215125 181215125 GCTCACCGCAACCTCCGCCTCCTGGTTCGAGCAATTCTTGTGCCTCAGCCTCCTAAGTAGCTGGG GCTCACCGCAACCTCCGCCTCCTGGTTCGAGCGATTCTTGTGCCTCAGCCTCCTAAGTAGCTGGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1271999989 Functional Loss SNV dbSNP153 33..33 33 - - - 14424 RMVar_ID_14424 Human_SNP_ID_41300557 A-to-I Human chr1 + 182395831 182395831 182395831 GATTTGAGTTTTGTAGGATGCGTGCTGAAATCAGTCAAATACAAGGAACACTTCATTTCCCCAAC GATTTGAGTTTTGTAGGATGCGTGCTGAAATCGGTCAAATACAAGGAACACTTCATTTCCCCAAC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs954285688 Functional Loss SNV dbSNP153 33..33 33 - - - 14425 RMVar_ID_14425 Human_SNP_ID_41413061 A-to-I Human chr1 + 182864281 182864281 182864281 ACTGATGTTTATTTTTGTAGAGATGGTGTCTCACTGTGTTGCCCAGGCTGGTCTTGAACTCGTTG ACTGATGTTTATTTTTGTAGAGATGGTGTCTCGCTGTGTTGCCCAGGCTGGTCTTGAACTCGTTG A G DHX9 Ensembl:ENSG00000135829 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs947475532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557395 RMVar_hsa_circ_296,RMVar_hsa_circ_118315,RMVar_hsa_circ_378808,RMVar_hsa_circ_64657,RMVar_hsa_circ_108757,RMVar_hsa_circ_41152,RMVar_hsa_circ_138189,RMVar_hsa_circ_138188,RMVar_hsa_circ_106250,RMVar_hsa_circ_369682,RMVar_hsa_circ_123950,RMVar_hsa_circ_51557,RMVar_hsa_circ_40506,RMVar_hsa_circ_28798,RMVar_hsa_circ_119190,RMVar_hsa_circ_138195,RMVar_hsa_circ_138196,RMVar_hsa_circ_138197,RMVar_hsa_circ_112008,RMVar_hsa_circ_113854,RMVar_hsa_circ_138199,RMVar_hsa_circ_138201,RMVar_hsa_circ_94850,RMVar_hsa_circ_138200,RMVar_hsa_circ_138198,RMVar_hsa_circ_8279,RMVar_hsa_circ_103340,RMVar_hsa_circ_321348,RMVar_hsa_circ_44981,RMVar_hsa_circ_36291,RMVar_hsa_circ_138203,RMVar_hsa_circ_375418,RMVar_hsa_circ_138206,RMVar_hsa_circ_41823,RMVar_hsa_circ_66236,RMVar_hsa_circ_138207,RMVar_hsa_circ_110746,RMVar_hsa_circ_78873,RMVar_hsa_circ_112234,RMVar_hsa_circ_138208,RMVar_hsa_circ_138209,RMVar_hsa_circ_138210 14426 RMVar_ID_14426 Human_SNP_ID_41466635 A-to-I Human chr1 + 183085442 183085442 183085442 TGGAGTGCAGTAGTGTGAATATGACTCACTGCAGCCTCGACCTCCCAGGCTCAAGGGATCCTCCC TGGAGTGCAGTAGTGTGAATATGACTCACTGCCGCCTCGACCTCCCAGGCTCAAGGGATCCTCCC A C LAMC1 Ensembl:ENSG00000135862 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs564047893 Functional Loss SNV dbSNP153 33..33 33 - - - 14427 RMVar_ID_14427 Human_SNP_ID_41563180 A-to-I Human chr1 + 183486550 183486550 183486550 CTCCTGCCTCAGCCTGCTGAGTAGCTGGGATTACAGGCGCCCGCCACCACGCCTGGCCGATTTTT CTCCTGCCTCAGCCTGCTGAGTAGCTGGGATTGCAGGCGCCCGCCACCACGCCTGGCCGATTTTT A G SMG7 Ensembl:ENSG00000116698 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs556042994 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_96256 RMVar_hsa_circ_138266,RMVar_hsa_circ_92252,RMVar_hsa_circ_107841,RMVar_hsa_circ_138267 14428 RMVar_ID_14428 Human_SNP_ID_41564720 A-to-I Human chr1 + 183493227 183493227 183493227 AAACTCTTGGCCTCAAGCGATCCCCTGGCCTCAGCCTCCCAAAGTGTTGAGATTACAGGTGTGAG AAACTCTTGGCCTCAAGCGATCCCCTGGCCTCCGCCTCCCAAAGTGTTGAGATTACAGGTGTGAG A C SMG7 Ensembl:ENSG00000116698 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1040816965 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_138266,RMVar_hsa_circ_92252,RMVar_hsa_circ_107841,RMVar_hsa_circ_138267 14429 RMVar_ID_14429 Human_SNP_ID_41564737 A-to-I Human chr1 + 183493289 183493289 183493289 GAGCCACTACACCCGGCAACCTATGATTATTTAGAAATGTTTGATTCATTTCCAAATATTTGAGG GAGCCACTACACCCGGCAACCTATGATTATTTGGAAATGTTTGATTCATTTCCAAATATTTGAGG A G SMG7 Ensembl:ENSG00000116698 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1470403632 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_138266,RMVar_hsa_circ_92252,RMVar_hsa_circ_107841,RMVar_hsa_circ_138267 14430 RMVar_ID_14430 Human_SNP_ID_41569349 A-to-I Human chr1 + 183513950 183513950 183513950 TACTCTGGAGGCTGAGGCAGGAGAATCACTTTAACTGGGGAGGTGGAGGTTGCAGTGAGCAGAGA TACTCTGGAGGCTGAGGCAGGAGAATCACTTTGACTGGGGAGGTGGAGGTTGCAGTGAGCAGAGA A G SMG7 Ensembl:ENSG00000116698 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1417722600 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24755212 RMVar_hsa_circ_11084,RMVar_hsa_circ_138266,RMVar_hsa_circ_92252,RMVar_hsa_circ_107841,RMVar_hsa_circ_138267,RMVar_hsa_circ_349729,RMVar_hsa_circ_355354,RMVar_hsa_circ_138270,RMVar_hsa_circ_97847,RMVar_hsa_circ_138269,RMVar_hsa_circ_374732,RMVar_hsa_circ_290400,RMVar_hsa_circ_138271 14431 RMVar_ID_14431 Human_SNP_ID_41571231 A-to-I Human chr1 + 183521762 183521762 183521762 TGGCGCACACCTGTAGTACCAGCTACTCTAGGAAGCTGAGGCAGGAGGATCACTTGAGCCCAGGA TGGCGCACACCTGTAGTACCAGCTACTCTAGGGAGCTGAGGCAGGAGGATCACTTGAGCCCAGGA A G SMG7 Ensembl:ENSG00000116698 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1442430120 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18504,RMVar_hsa_circ_11084,RMVar_hsa_circ_138266,RMVar_hsa_circ_92252,RMVar_hsa_circ_107841,RMVar_hsa_circ_138267,RMVar_hsa_circ_349729,RMVar_hsa_circ_138270,RMVar_hsa_circ_97847,RMVar_hsa_circ_83881,RMVar_hsa_circ_360984,RMVar_hsa_circ_100807,RMVar_hsa_circ_59877,RMVar_hsa_circ_57829,RMVar_hsa_circ_138273,RMVar_hsa_circ_138274,RMVar_hsa_circ_375589,RMVar_hsa_circ_104690,RMVar_hsa_circ_366830,RMVar_hsa_circ_86157,RMVar_hsa_circ_52702,RMVar_hsa_circ_54076,RMVar_hsa_circ_138276,RMVar_hsa_circ_138278,RMVar_hsa_circ_46487,RMVar_hsa_circ_138277 14432 RMVar_ID_14432 Human_SNP_ID_41580580 A-to-I Human chr1 - 183559656 183559656 183559656 TGGGGTTTTGCCATGTTGACCAGGCTGGTCTCAAACTCCTGGCCTCAAGTGATCCAACTGCCTCG TGGGGTTTTGCCATGTTGACCAGGCTGGTCTCCAACTCCTGGCCTCAAGTGATCCAACTGCCTCG T G NCF2 Ensembl:ENSG00000116701 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277321655 Functional Loss SNV dbSNP153 33..33 33 - - - 14433 RMVar_ID_14433 Human_SNP_ID_41865581 A-to-I Human chr1 - 184791989 184791989 184791989 TTTTACCACTGCACTCCAGCTTGGGCAACAAAATGAGACCCTGTCTCAAAAAAAAAAAAAAAGTT TTTTACCACTGCACTCCAGCTTGGGCAACAAAGTGAGACCCTGTCTCAAAAAAAAAAAAAAAGTT T C NIBAN1 Ensembl:ENSG00000135842 Protein coding intron GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,29796672,31158229,31158229,31158229 RNA-Seq:(High) rs1380837996 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85019,RMVar_hsa_circ_138340 14434 RMVar_ID_14434 Human_SNP_ID_41865592 A-to-I Human chr1 - 184792045 184792045 184792045 GGTTGAGGCAGGAGGATTGTTTGAGCGAGGGAAGTTGAGGCTGCAGTGAACTATGATTTTACCAC GGTTGAGGCAGGAGGATTGTTTGAGCGAGGGAGGTTGAGGCTGCAGTGAACTATGATTTTACCAC T C NIBAN1 Ensembl:ENSG00000135842 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1139072 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5728003,Human_RBP_ID_26386805 RMVar_hsa_circ_85019,RMVar_hsa_circ_138340 14435 RMVar_ID_14435 Human_SNP_ID_41865595 A-to-I Human chr1 - 184792054 184792054 184792054 TACTTGGGTGGTTGAGGCAGGAGGATTGTTTGAGCGAGGGAAGTTGAGGCTGCAGTGAACTATGA TACTTGGGTGGTTGAGGCAGGAGGATTGTTTGGGCGAGGGAAGTTGAGGCTGCAGTGAACTATGA T C NIBAN1 Ensembl:ENSG00000135842 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs3180402 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5728003,Human_RBP_ID_26388989 Human_miRNA_ID_1098769,Human_miRNA_ID_2516170 RMVar_hsa_circ_85019,RMVar_hsa_circ_138340 14436 RMVar_ID_14436 Human_SNP_ID_41865601 A-to-I Human chr1 - 184792089 184792089 184792089 AAAAAATAATAATGGTGTGTGCCTGCAGTCCTAGCTACTTGGGTGGTTGAGGCAGGAGGATTGTT AAAAAATAATAATGGTGTGTGCCTGCAGTCCTCGCTACTTGGGTGGTTGAGGCAGGAGGATTGTT T G NIBAN1 Ensembl:ENSG00000135842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1292481369 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26388990 RMVar_hsa_circ_85019,RMVar_hsa_circ_138340 14437 RMVar_ID_14437 Human_SNP_ID_41865605 A-to-I Human chr1 - 184792095 184792095 184792095 CCTTACAAAAAATAATAATGGTGTGTGCCTGCAGTCCTAGCTACTTGGGTGGTTGAGGCAGGAGG CCTTACAAAAAATAATAATGGTGTGTGCCTGCTGTCCTAGCTACTTGGGTGGTTGAGGCAGGAGG T A NIBAN1 Ensembl:ENSG00000135842 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs112320565 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26388990 Human_miRNA_ID_617790 RMVar_hsa_circ_85019,RMVar_hsa_circ_138340 14438 RMVar_ID_14438 Human_SNP_ID_41865606 A-to-I Human chr1 - 184792095 184792095 184792095 CCTTACAAAAAATAATAATGGTGTGTGCCTGCAGTCCTAGCTACTTGGGTGGTTGAGGCAGGAGG CCTTACAAAAAATAATAATGGTGTGTGCCTGCGGTCCTAGCTACTTGGGTGGTTGAGGCAGGAGG T C NIBAN1 Ensembl:ENSG00000135842 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs112320565 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26388990 Human_miRNA_ID_617790 RMVar_hsa_circ_85019,RMVar_hsa_circ_138340 14439 RMVar_ID_14439 Human_SNP_ID_41865616 A-to-I Human chr1 - 184792140 184792140 184792140 GCCCAGGAGTTCTAGACAAGCCTGGGAAACATAGCAAGATCTCATCCTTACAAAAAATAATAATG GCCCAGGAGTTCTAGACAAGCCTGGGAAACATGGCAAGATCTCATCCTTACAAAAAATAATAATG T C NIBAN1 Ensembl:ENSG00000135842 Protein coding intron GSE38233;GSE100210;GSE112787 cultured B-cells;HepG2 cell line;293 Flip-In T-REx cells,empty vector - 24183664,29129909,29967493 RNA-Seq:(High) rs1139070 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85019,RMVar_hsa_circ_138340 14440 RMVar_ID_14440 Human_SNP_ID_41865625 A-to-I Human chr1 - 184792178 184792178 184792178 CCAGCACTTTGGGAGGCTGAGGTGAGAGGGTCACTTGAGCCCAGGAGTTCTAGACAAGCCTGGGA CCAGCACTTTGGGAGGCTGAGGTGAGAGGGTCGCTTGAGCCCAGGAGTTCTAGACAAGCCTGGGA T C NIBAN1 Ensembl:ENSG00000135842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1139069 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26388991 RMVar_hsa_circ_85019,RMVar_hsa_circ_138340 14441 RMVar_ID_14441 Human_SNP_ID_41865626 A-to-I Human chr1 - 184792178 184792178 184792178 CCAGCACTTTGGGAGGCTGAGGTGAGAGGGTCACTTGAGCCCAGGAGTTCTAGACAAGCCTGGGA CCAGCACTTTGGGAGGCTGAGGTGAGAGGGTCCCTTGAGCCCAGGAGTTCTAGACAAGCCTGGGA T G NIBAN1 Ensembl:ENSG00000135842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1139069 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26388991 RMVar_hsa_circ_85019,RMVar_hsa_circ_138340 14442 RMVar_ID_14442 Human_SNP_ID_41865632 A-to-I Human chr1 - 184792216 184792216 184792216 AGTTTTTGGGCTGGATGTGGTAGCTTACACCTATAATCCCAGCACTTTGGGAGGCTGAGGTGAGA AGTTTTTGGGCTGGATGTGGTAGCTTACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGAGA T C NIBAN1 Ensembl:ENSG00000135842 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,31158229,32596459 RNA-Seq:(High) rs1283162939 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85019,RMVar_hsa_circ_138340 14443 RMVar_ID_14443 Human_SNP_ID_41865884 A-to-I Human chr1 - 184793338 184793338 184793338 TTGGCCAGGCTGGTCTCAAACTCCTGATTTCAAGCGATCCACCCACCTCGACTTCCCAAAGTGCT TTGGCCAGGCTGGTCTCAAACTCCTGATTTCAGGCGATCCACCCACCTCGACTTCCCAAAGTGCT T C NIBAN1 Ensembl:ENSG00000135842 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1266595555 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27392022 RMVar_hsa_circ_85019,RMVar_hsa_circ_138340 14444 RMVar_ID_14444 Human_SNP_ID_41865894 A-to-I Human chr1 - 184793390 184793390 184793390 CACCATTCCCGGCTAATTTTTGTATTTTTGGTAGAGATGGGTTTTCACCATGTTGGCCAGGCTGG CACCATTCCCGGCTAATTTTTGTATTTTTGGTGGAGATGGGTTTTCACCATGTTGGCCAGGCTGG T C NIBAN1 Ensembl:ENSG00000135842 Protein coding intron GSE38233;GSE100210;GSE99789;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,29796672,32596459 RNA-Seq:(High) rs940823216 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85019,RMVar_hsa_circ_138340 14445 RMVar_ID_14445 Human_SNP_ID_41865925 A-to-I Human chr1 - 184793493 184793493 184793493 GGAGTGCAGTGGTGTGATCTCGGCTCACTGCAACCTCCGCCTCCTGGGTTCAGGAGATTCTCCTC GGAGTGCAGTGGTGTGATCTCGGCTCACTGCATCCTCCGCCTCCTGGGTTCAGGAGATTCTCCTC T A NIBAN1 Ensembl:ENSG00000135842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1055821882 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24399926,Human_RBP_ID_26386806 RMVar_hsa_circ_85019,RMVar_hsa_circ_138340 14446 RMVar_ID_14446 Human_SNP_ID_41869865 A-to-I Human chr1 - 184807641 184807641 184807641 GGGACTACAGGCATGTGCCACCATGTCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTTT GGGACTACAGGCATGTGCCACCATGTCTGGCTGATTTTTGTATTTTTAGTAGAGATGGGGTTTTT T C NIBAN1 Ensembl:ENSG00000135842 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs373729434 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85019,RMVar_hsa_circ_138341,RMVar_hsa_circ_104937,RMVar_hsa_circ_127453,RMVar_hsa_circ_138340,RMVar_hsa_circ_138342,RMVar_hsa_circ_103249,RMVar_hsa_circ_138343 14447 RMVar_ID_14447 Human_SNP_ID_41885274 A-to-I Human chr1 - 184876589 184876589 184876589 TCAAGAGGTTCTCCTGCCTCAGCCTCTAGAGTAGCTGGGATTACAAGCGCACACTACCACACCTG TCAAGAGGTTCTCCTGCCTCAGCCTCTAGAGTGGCTGGGATTACAAGCGCACACTACCACACCTG T C NIBAN1 Ensembl:ENSG00000135842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1374627179 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85019,RMVar_hsa_circ_138340 14448 RMVar_ID_14448 Human_SNP_ID_41904300 A-to-I Human chr1 - 184958829 184958829 184958829 TCTGGAGTATAAATATTTAAAATGGTTTTGTTAGAGAGGAGAATTAAATTAGTAACAATAATTGA TCTGGAGTATAAATATTTAAAATGGTTTTGTTGGAGAGGAGAATTAAATTAGTAACAATAATTGA T C NIBAN1 Ensembl:ENSG00000135842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1472968358 Functional Loss SNV dbSNP153 33..33 33 - - - 14449 RMVar_ID_14449 Human_SNP_ID_41904315 A-to-I Human chr1 - 184958893 184958893 184958893 CAGATGCAGGCTTAGAGTTAAAATAAAGCCAAATTTTATGAGCAACAATGGCAAATGTGTAATAT CAGATGCAGGCTTAGAGTTAAAATAAAGCCAAGTTTTATGAGCAACAATGGCAAATGTGTAATAT T C NIBAN1 Ensembl:ENSG00000135842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1439997778 Functional Loss SNV dbSNP153 33..33 33 - - - 14450 RMVar_ID_14450 Human_SNP_ID_42263737 A-to-I Human chr1 + 186417215 186417215 186417215 GAACTCCTGAGCTCAGGCACTCTGCCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTCAG GAACTCCTGAGCTCAGGCACTCTGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTCAG A G ODR4 Ensembl:ENSG00000157181 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs564733983 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22560975 RMVar_hsa_circ_31316,RMVar_hsa_circ_138466,RMVar_hsa_circ_138470,RMVar_hsa_circ_138465,RMVar_hsa_circ_138468,RMVar_hsa_circ_138469,RMVar_hsa_circ_138467,RMVar_hsa_circ_138481,RMVar_hsa_circ_33193,RMVar_hsa_circ_377339,RMVar_hsa_circ_316939,RMVar_hsa_circ_266664,RMVar_hsa_circ_138483,RMVar_hsa_circ_138482,RMVar_hsa_circ_138477,RMVar_hsa_circ_138479,RMVar_hsa_circ_138480,RMVar_hsa_circ_138478,RMVar_hsa_circ_138476,RMVar_hsa_circ_138486 14451 RMVar_ID_14451 Human_SNP_ID_42292652 A-to-I Human chr1 + 186542772 186542772 186542772 ATCACTCCTGGATAATTTTTTAAATTTTTAGTAGAGATGGGGTTTCGTCATGCTGGCCAGGCTGG ATCACTCCTGGATAATTTTTTAAATTTTTAGTGGAGATGGGGTTTCGTCATGCTGGCCAGGCTGG A G PDC-AS1 RNACentral:URS00009B8F3A lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1248778441 Functional Loss SNV dbSNP153 33..33 33 - - - 14452 RMVar_ID_14452 Human_SNP_ID_42545059 A-to-I Human chr1 + 187563409 187563409 187563409 TGCCGGGGACAGATCTGCTGGTATCAGAAGCCAGGCATGGATTTAGATGCCATCAATGATGTTAT TGCCGGGGACAGATCTGCTGGTATCAGAAGCCGGGCATGGATTTAGATGCCATCAATGATGTTAT A G ERVMER61-1,FDPSP1 Ensembl:ENSG00000230426,Ensembl:ENSG00000225462 lincRNA,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1261794866 Functional Loss SNV dbSNP153 33..33 33 - - - 14453 RMVar_ID_14453 Human_SNP_ID_43943570 A-to-I Human chr1 - 192992882 192992882 192992882 TGGCTCACACCTGTAATCCCAGCACTTTGGGAAGCTGAGGTGGGAGGATCACTTGAGCCCGGGAG TGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGAGGATCACTTGAGCCCGGGAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017632832 Functional Loss SNV dbSNP153 33..33 33 - - - 14454 RMVar_ID_14454 Human_SNP_ID_43966443 A-to-I Human chr1 + 193091422 193091422 193091422 AAGTTATGTAAAATCTGATTTAAGTTTATTTCATTTCCAAGGAAAGGACCCTGAAAGGAGGGGAC AAGTTATGTAAAATCTGATTTAAGTTTATTTCGTTTCCAAGGAAAGGACCCTGAAAGGAGGGGAC A G RO60 Ensembl:ENSG00000116747 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs892785218 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_336479,Human_RBP_ID_2112335,Human_RBP_ID_3290825,Human_RBP_ID_4086455,Human_RBP_ID_5732329,Human_RBP_ID_8739784,Human_RBP_ID_10705632,Human_RBP_ID_17214527,Human_RBP_ID_17332222,Human_RBP_ID_17448307,Human_RBP_ID_18221506,Human_RBP_ID_26373486,Human_RBP_ID_27583764 14455 RMVar_ID_14455 Human_SNP_ID_43966455 A-to-I Human chr1 + 193091484 193091484 193091484 GACAGGGAGCTTCCTAGGTCTGTTGATAAACTAACTGATGCTTTGTCAAGTCTTCCAAGTTTTCA GACAGGGAGCTTCCTAGGTCTGTTGATAAACTGACTGATGCTTTGTCAAGTCTTCCAAGTTTTCA A G RO60 Ensembl:ENSG00000116747 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs542589402 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_336482,Human_RBP_ID_1417701,Human_RBP_ID_1732065,Human_RBP_ID_2112336,Human_RBP_ID_3290826,Human_RBP_ID_8739785,Human_RBP_ID_17448309,Human_RBP_ID_18221507,Human_RBP_ID_21880812,Human_RBP_ID_21911692,Human_RBP_ID_23352656 14456 RMVar_ID_14456 Human_SNP_ID_43966731 A-to-I Human chr1 - 193092687 193092687 193092687 GTAAATATGGGGGTCTTACTGTGTTGCCCAGCAAGATCCCCATAGTTACAACTTTTTAGTTTTGA GTAAATATGGGGGTCTTACTGTGTTGCCCAGCGAGATCCCCATAGTTACAACTTTTTAGTTTTGA T C GLRX2 Ensembl:ENSG00000023572 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232504111 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5732354,Human_RBP_ID_17448319 14457 RMVar_ID_14457 Human_SNP_ID_43967357 A-to-I Human chr1 - 193095397 193095397 193095397 TCAAGCAATTCTCCTGCCTCAGCATCCTGAGTAGCTGGGATCACATGTGCCCGCCACCGCACCTG TCAAGCAATTCTCCTGCCTCAGCATCCTGAGTGGCTGGGATCACATGTGCCCGCCACCGCACCTG T C GLRX2 Ensembl:ENSG00000023572 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs891996812 Functional Loss SNV dbSNP153 33..33 33 - - - 14458 RMVar_ID_14458 Human_SNP_ID_43967509 A-to-I Human chr1 - 193095840 193095840 193095840 CAGGTGTTGGAGATCAGCTTGGTCTACATAGCAAGACCCCCATATTTACAACAAATAAACAAAAA CAGGTGTTGGAGATCAGCTTGGTCTACATAGCGAGACCCCCATATTTACAACAAATAAACAAAAA T C GLRX2 Ensembl:ENSG00000023572 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs960017548 Functional Loss SNV dbSNP153 33..33 33 - - - 14459 RMVar_ID_14459 Human_SNP_ID_43983472 A-to-I Human chr1 + 193158404 193158404 193158404 TGATTTTCTGGACAGGATGGTGGCTCACAGCTATAATCCTAGAACTTTGGGAGGCTGAGGCAGGA TGATTTTCTGGACAGGATGGTGGCTCACAGCTGTAATCCTAGAACTTTGGGAGGCTGAGGCAGGA A G CDC73 Ensembl:ENSG00000134371 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs543312833 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24618350 RMVar_hsa_circ_99976,RMVar_hsa_circ_121800,RMVar_hsa_circ_138539,RMVar_hsa_circ_138538,RMVar_hsa_circ_303094,RMVar_hsa_circ_90009,RMVar_hsa_circ_138542,RMVar_hsa_circ_111424,RMVar_hsa_circ_138545,RMVar_hsa_circ_12477 14460 RMVar_ID_14460 Human_SNP_ID_43986124 A-to-I Human chr1 + 193166700 193166700 193166700 AGACCGAGTTTTGCTCTTGTTGCCCCTGGAGTACAGTGGAGCTATCTTGGCTCACCACAACCTCT AGACCGAGTTTTGCTCTTGTTGCCCCTGGAGTTCAGTGGAGCTATCTTGGCTCACCACAACCTCT A T CDC73 Ensembl:ENSG00000134371 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1261152691 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10706573 RMVar_hsa_circ_99976,RMVar_hsa_circ_121800,RMVar_hsa_circ_138539,RMVar_hsa_circ_138538,RMVar_hsa_circ_303094,RMVar_hsa_circ_90009,RMVar_hsa_circ_138542,RMVar_hsa_circ_111424,RMVar_hsa_circ_138545,RMVar_hsa_circ_12477 14461 RMVar_ID_14461 Human_SNP_ID_43986556 A-to-I Human chr1 + 193168583 193168583 193168583 AGTCTCTCTCTGTCACCCAGATGGAATGCAGTAGCGCAATCTTGCCTCACTGCACCCTCCATTTC AGTCTCTCTCTGTCACCCAGATGGAATGCAGTGGCGCAATCTTGCCTCACTGCACCCTCCATTTC A G CDC73 Ensembl:ENSG00000134371 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs960992098 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99976,RMVar_hsa_circ_121800,RMVar_hsa_circ_138539,RMVar_hsa_circ_138538,RMVar_hsa_circ_303094,RMVar_hsa_circ_90009,RMVar_hsa_circ_138542,RMVar_hsa_circ_111424,RMVar_hsa_circ_138545,RMVar_hsa_circ_12477 14462 RMVar_ID_14462 Human_SNP_ID_43986764 A-to-I Human chr1 + 193169422 193169422 193169422 CAAAAATTAGCTGGGCGTGGTGGCACATGCCTATGATCCCAGCTGCTAAAGAGGCTGAGGTAGGA CAAAAATTAGCTGGGCGTGGTGGCACATGCCTGTGATCCCAGCTGCTAAAGAGGCTGAGGTAGGA A G CDC73 Ensembl:ENSG00000134371 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1007356191 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99976,RMVar_hsa_circ_121800,RMVar_hsa_circ_138539,RMVar_hsa_circ_138538,RMVar_hsa_circ_303094,RMVar_hsa_circ_90009,RMVar_hsa_circ_138542,RMVar_hsa_circ_111424,RMVar_hsa_circ_138545,RMVar_hsa_circ_12477 14463 RMVar_ID_14463 Human_SNP_ID_43997796 A-to-I Human chr1 + 193212397 193212397 193212397 CTACCTGTAAATTTTGTCTTTATAGGATCTCGAACACCCATTATCATAATTCCTGCAGCTACCAC CTACCTGTAAATTTTGTCTTTATAGGATCTCGGACACCCATTATCATAATTCCTGCAGCTACCAC A G CDC73 Ensembl:ENSG00000134371 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs3203682 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_851921,Human_RBP_ID_9357368,Human_RBP_ID_10707471,Human_RBP_ID_17214538,Human_RBP_ID_17332235,Human_RBP_ID_17448326,Human_RBP_ID_17734434,Human_RBP_ID_24747691,Human_RBP_ID_27392129,Human_RBP_ID_27801322 Human_Splice_Rec_168386,Human_Splice_Rec_168387,Human_Splice_Rec_168416,Human_Splice_Rec_168417,Human_Splice_Rec_168446,Human_Splice_Rec_168447,Human_Splice_Rec_168476,Human_Splice_Rec_168477,Human_Splice_Rec_168528,Human_Splice_Rec_168529,Human_Splice_Rec_168554,Human_Splice_Rec_168555,Human_Splice_Rec_168628,Human_Splice_Rec_168629 RMVar_hsa_circ_138550,RMVar_hsa_circ_99976,RMVar_hsa_circ_121800,RMVar_hsa_circ_138539,RMVar_hsa_circ_138538,RMVar_hsa_circ_90009,RMVar_hsa_circ_138542,RMVar_hsa_circ_138547,RMVar_hsa_circ_300290,RMVar_hsa_circ_365130,RMVar_hsa_circ_12477,RMVar_hsa_circ_356831,RMVar_hsa_circ_287323,RMVar_hsa_circ_138548,RMVar_hsa_circ_112742,RMVar_hsa_circ_327704,RMVar_hsa_circ_367463,RMVar_hsa_circ_138546,RMVar_hsa_circ_330997,RMVar_hsa_circ_303810,RMVar_hsa_circ_138552,RMVar_hsa_circ_138553,RMVar_hsa_circ_138551 14464 RMVar_ID_14464 Human_SNP_ID_44004288 A-to-I Human chr1 + 193237013 193237013 193237013 TCGCCCAGGCTGGATTGCAGTGGCGCGATCTCAGCTCACTGCAAGCTCCGCCTCCCGGGTTCACG TCGCCCAGGCTGGATTGCAGTGGCGCGATCTCCGCTCACTGCAAGCTCCGCCTCCCGGGTTCACG A C CDC73 Ensembl:ENSG00000134371 Protein coding exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1367602471 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_168392 RMVar_hsa_circ_99976,RMVar_hsa_circ_138539,RMVar_hsa_circ_356831,RMVar_hsa_circ_112742,RMVar_hsa_circ_367463,RMVar_hsa_circ_138552,RMVar_hsa_circ_138553,RMVar_hsa_circ_138555,RMVar_hsa_circ_349158 14465 RMVar_ID_14465 Human_SNP_ID_44004289 A-to-I Human chr1 + 193237013 193237013 193237013 TCGCCCAGGCTGGATTGCAGTGGCGCGATCTCAGCTCACTGCAAGCTCCGCCTCCCGGGTTCACG TCGCCCAGGCTGGATTGCAGTGGCGCGATCTCTGCTCACTGCAAGCTCCGCCTCCCGGGTTCACG A T CDC73 Ensembl:ENSG00000134371 Protein coding exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1367602471 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_168392 RMVar_hsa_circ_99976,RMVar_hsa_circ_138539,RMVar_hsa_circ_356831,RMVar_hsa_circ_112742,RMVar_hsa_circ_367463,RMVar_hsa_circ_138552,RMVar_hsa_circ_138553,RMVar_hsa_circ_138555,RMVar_hsa_circ_349158 14466 RMVar_ID_14466 Human_SNP_ID_44004291 A-to-I Human chr1 + 193237018 193237018 193237018 CAGGCTGGATTGCAGTGGCGCGATCTCAGCTCACTGCAAGCTCCGCCTCCCGGGTTCACGCCATT CAGGCTGGATTGCAGTGGCGCGATCTCAGCTCGCTGCAAGCTCCGCCTCCCGGGTTCACGCCATT A G CDC73 Ensembl:ENSG00000134371 Protein coding exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1370406533 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_168392 RMVar_hsa_circ_99976,RMVar_hsa_circ_138539,RMVar_hsa_circ_356831,RMVar_hsa_circ_112742,RMVar_hsa_circ_367463,RMVar_hsa_circ_138552,RMVar_hsa_circ_138553,RMVar_hsa_circ_138555,RMVar_hsa_circ_349158 14467 RMVar_ID_14467 Human_SNP_ID_44004313 A-to-I Human chr1 + 193237077 193237077 193237077 GCCATTCTCCTGCCTCAACCTCCTGAGTAGCTAGGACTACAGGCGTCCGCCACCACGCCCGGCTA GCCATTCTCCTGCCTCAACCTCCTGAGTAGCTGGGACTACAGGCGTCCGCCACCACGCCCGGCTA A G CDC73 Ensembl:ENSG00000134371 Protein coding exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1035240481 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99976,RMVar_hsa_circ_138539,RMVar_hsa_circ_356831,RMVar_hsa_circ_112742,RMVar_hsa_circ_367463,RMVar_hsa_circ_138552,RMVar_hsa_circ_138553,RMVar_hsa_circ_138555,RMVar_hsa_circ_349158 14468 RMVar_ID_14468 Human_SNP_ID_44016614 A-to-I Human chr1 + 193287080 193287080 193287080 TGAGCTGAGATGGTGCCACTGCACCCCAGCATAGGCAACAGAGTGAGACCCTGTCTAAAAAAAAA TGAGCTGAGATGGTGCCACTGCACCCCAGCATCGGCAACAGAGTGAGACCCTGTCTAAAAAAAAA A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs930041807 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_138556 14469 RMVar_ID_14469 Human_SNP_ID_44016615 A-to-I Human chr1 + 193287080 193287080 193287080 TGAGCTGAGATGGTGCCACTGCACCCCAGCATAGGCAACAGAGTGAGACCCTGTCTAAAAAAAAA TGAGCTGAGATGGTGCCACTGCACCCCAGCATGGGCAACAGAGTGAGACCCTGTCTAAAAAAAAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs930041807 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_138556 14470 RMVar_ID_14470 Human_SNP_ID_139326229 A-to-I Human chr3 - 75416686 75416681 75416686 CACCATACCTAGCTAATTTTTGTATTTTTAGTAGAGACAGTTTTCACCATGTTGGCCAGGTTGGT CACCATACCTAGCTAATTTTTGTATTTTTAGT_____CAGTTTTCACCATGTTGGCCAGGTTGGT GTCTCT G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1160851314 Functional Loss DEL dbSNP153 33..37 33 - - - 14471 RMVar_ID_14471 Human_SNP_ID_139326232 A-to-I Human chr3 - 75416689 75416687 75416689 CACCACCATACCTAGCTAATTTTTGTATTTTTAGTAGAGACAGTTTTCACCATGTTGGCCAGGTT CACCACCATACCTAGCTAATTTTTGTATTTTT__TAGAGACAGTTTTCACCATGTTGGCCAGGTT ACT A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1465907198 Functional Loss DEL dbSNP153 33..34 33 - - - 14472 RMVar_ID_14472 Human_SNP_ID_139326234 A-to-I Human chr3 - 75416689 75416689 75416689 CACCACCATACCTAGCTAATTTTTGTATTTTTAGTAGAGACAGTTTTCACCATGTTGGCCAGGTT CACCACCATACCTAGCTAATTTTTGTATTTTTTGTAGAGACAGTTTTCACCATGTTGGCCAGGTT T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1162507965 Functional Loss SNV dbSNP153 33..33 33 - - - 14473 RMVar_ID_14473 Human_SNP_ID_139328433 A-to-I Human chr3 - 75423499 75423499 75423499 TTTTTGTATTTTCGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGAAGA TTTTTGTATTTTCGTAGAGATGGGGTTTCACCTTGTTGGCCAGGCTGGTCTCGAACTCCTGAAGA T A FAM86DP Ensembl:ENSG00000244026 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1489687368 Functional Loss SNV dbSNP153 33..33 33 - - - 14474 RMVar_ID_14474 Human_SNP_ID_139328975 A-to-I Human chr3 - 75425150 75425150 75425150 CCGCCCACCTTTTTTTTTTTTTTTTCTTTTTGAGACAGAGTCTGGCTTTGTATTGCCCAGGCTGG CCGCCCACCTTTTTTTTTTTTTTTTCTTTTTGGGACAGAGTCTGGCTTTGTATTGCCCAGGCTGG T C FAM86DP Ensembl:ENSG00000244026 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs757580070 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17573766 14475 RMVar_ID_14475 Human_SNP_ID_139329119 A-to-I Human chr3 - 75425431 75425431 75425431 GAAACTAGCCAGATGTGGTTGCACACACCTGTAGTCCCAGCTACTCAGGAGGCTGAGGTGGGAGG GAAACTAGCCAGATGTGGTTGCACACACCTGTGGTCCCAGCTACTCAGGAGGCTGAGGTGGGAGG T C FAM86DP Ensembl:ENSG00000244026 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1463047879 Functional Loss SNV dbSNP153 33..33 33 - - - 14476 RMVar_ID_14476 Human_SNP_ID_139329138 A-to-I Human chr3 - 75425492 75425492 75425492 CCCCAGTTGTTCAAGAAAAACCTGGGCCACATAGTGGGACCCTGTCTTCACAAAACATACAGAAA CCCCAGTTGTTCAAGAAAAACCTGGGCCACATGGTGGGACCCTGTCTTCACAAAACATACAGAAA T C FAM86DP Ensembl:ENSG00000244026 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1392690866 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14979738 14477 RMVar_ID_14477 Human_SNP_ID_139329170 A-to-I Human chr3 - 75425574 75425574 75425574 CTCGCACAGGAGGCTGGCCGGGCGCGGGGCTCAGGCCTGTCATCCCGGCACTTTAGGAGGCTAAG CTCGCACAGGAGGCTGGCCGGGCGCGGGGCTCTGGCCTGTCATCCCGGCACTTTAGGAGGCTAAG T A FAM86DP Ensembl:ENSG00000244026 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1045027419 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5208784,Human_RBP_ID_8211015,Human_RBP_ID_18814468 14478 RMVar_ID_14478 Human_SNP_ID_139336199 A-to-I Human chr3 + 75445469 75445469 75445469 ACTCAACACCCCCGTGCTCAAGCAGTTCTCCCACCTCAGCCTCCTGAGTTGCTGGGACCACAGGC ACTCAACACCCCCGTGCTCAAGCAGTTCTCCCCCCTCAGCCTCCTGAGTTGCTGGGACCACAGGC A C LINC02018 Ensembl:ENSG00000272690 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1301747955 Functional Loss SNV dbSNP153 33..33 33 - - - 14479 RMVar_ID_14479 Human_SNP_ID_139418214 A-to-I Human chr3 + 75680627 75680627 75680627 TTACCTGATTTCAAACTATATCGTAAGACCATAGTCACCAAAACAGCATGGTTCTGGTATAAAAA TTACCTGATTTCAAACTATATCGTAAGACCATGGTCACCAAAACAGCATGGTTCTGGTATAAAAA A G LINC00960 Ensembl:ENSG00000242516 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1213623075 Functional Loss SNV dbSNP153 33..33 33 - - - 14480 RMVar_ID_14480 Human_SNP_ID_139439482 A-to-I Human chr3 - 75734645 75734645 75734645 AGATCATGAGGTCAGGAGATTGAGACCATCCTAGCTAAATGGTGAAATCCCATCTCTACTAAAAA AGATCATGAGGTCAGGAGATTGAGACCATCCTGGCTAAATGGTGAAATCCCATCTCTACTAAAAA T C ZNF717 Ensembl:ENSG00000227124 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1208934147 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37321 14481 RMVar_ID_14481 Human_SNP_ID_139442790 A-to-I Human chr3 - 75740799 75740799 75740799 AACAGATGATTCTCACTCTATTTCTCAGACTGAAGTGCAGTGGCATGATTATAGTTCACTGTAAT AACAGATGATTCTCACTCTATTTCTCAGACTGGAGTGCAGTGGCATGATTATAGTTCACTGTAAT T C ZNF717 Ensembl:ENSG00000227124 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1381510925 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_608293,Human_RBP_ID_27059158 RMVar_hsa_circ_37321,RMVar_hsa_circ_72778 14482 RMVar_ID_14482 Human_SNP_ID_139442791 A-to-I Human chr3 - 75740799 75740799 75740799 AACAGATGATTCTCACTCTATTTCTCAGACTGAAGTGCAGTGGCATGATTATAGTTCACTGTAAT AACAGATGATTCTCACTCTATTTCTCAGACTGCAGTGCAGTGGCATGATTATAGTTCACTGTAAT T G ZNF717 Ensembl:ENSG00000227124 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1381510925 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_608293,Human_RBP_ID_27059158 RMVar_hsa_circ_37321,RMVar_hsa_circ_72778 14483 RMVar_ID_14483 Human_SNP_ID_139449898 A-to-I Human chr3 - 75756771 75756771 75756771 ACTCGGGAGGCTGAGGCAGGAGAATGGCTTGAACTTGGGAGGCAGAGGTTGCGATGAGCCGAGAT ACTCGGGAGGCTGAGGCAGGAGAATGGCTTGAGCTTGGGAGGCAGAGGTTGCGATGAGCCGAGAT T C ZNF717 Ensembl:ENSG00000227124 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1224026036 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_156557 RMVar_hsa_circ_95914,RMVar_hsa_circ_219693 14484 RMVar_ID_14484 Human_SNP_ID_139632018 A-to-I Human chr3 - 76434760 76434760 76434760 CCCCTGATTAATCTGCGCAAACAGGGCTGAGCAGGAAGCGGACTCATCTGAGCCTCAACTGGTAG CCCCTGATTAATCTGCGCAAACAGGGCTGAGCGGGAAGCGGACTCATCTGAGCCTCAACTGGTAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1447029483 Functional Loss SNV dbSNP153 33..33 33 - - - 14485 RMVar_ID_14485 Human_SNP_ID_139651407 A-to-I Human chr3 + 76510613 76510613 76510613 AGATGTGGTGGCAGGCACCTTTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATTACTTGAA AGATGTGGTGGCAGGCACCTTTAGTCCCAGCTCCTTGGGAGGCTGAGGCAGGAGAATTACTTGAA A C ROBO2 Ensembl:ENSG00000185008 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs551148402 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_219711 14486 RMVar_ID_14486 Human_SNP_ID_140065618 A-to-I Human chr3 - 78147014 78147014 78147014 AAATTATCCGAGTGTGGTGACGGGCGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAA AAATTATCCGAGTGTGGTGACGGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs547213646 Functional Loss SNV dbSNP153 33..33 33 - - - 14487 RMVar_ID_14487 Human_SNP_ID_140234478 A-to-I Human chr3 - 78816825 78816825 78816825 ATTTCAAGGAACTACTTCCTTTGCTTATCCATAAGAAGTGACTCTTCATCTGTTCAAGTTTTCTC ATTTCAAGGAACTACTTCCTTTGCTTATCCATGAGAAGTGACTCTTCATCTGTTCAAGTTTTCTC T C ROBO1 Ensembl:ENSG00000169855 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs958976695 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86565,RMVar_hsa_circ_219767,RMVar_hsa_circ_309476,RMVar_hsa_circ_342781 14488 RMVar_ID_14488 Human_SNP_ID_140258766 A-to-I Human chr3 - 78917237 78917237 78917237 CCAAAATTAACTGGGTGTGGTGGCGGGCACCTATAATCTTGGCTACTTAGGAGGCTGAGGCAGGA CCAAAATTAACTGGGTGTGGTGGCGGGCACCTGTAATCTTGGCTACTTAGGAGGCTGAGGCAGGA T C ROBO1 Ensembl:ENSG00000169855 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs888415520 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86565,RMVar_hsa_circ_219767,RMVar_hsa_circ_309476,RMVar_hsa_circ_342781,RMVar_hsa_circ_219790 14489 RMVar_ID_14489 Human_SNP_ID_140929800 A-to-I Human chr3 - 81524095 81524095 81524095 CTCATACACTGTTGGTGGGGTTGTCAATCAGTACAGCCAGTATGGAGAACAGTATGGAGATTACT CTCATACACTGTTGGTGGGGTTGTCAATCAGTGCAGCCAGTATGGAGAACAGTATGGAGATTACT T C GBE1 Ensembl:ENSG00000114480 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs926902310 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85315,RMVar_hsa_circ_107938,RMVar_hsa_circ_124462,RMVar_hsa_circ_119461,RMVar_hsa_circ_100562,RMVar_hsa_circ_96350,RMVar_hsa_circ_22294,RMVar_hsa_circ_219807,RMVar_hsa_circ_219809,RMVar_hsa_circ_219811,RMVar_hsa_circ_219812,RMVar_hsa_circ_219810,RMVar_hsa_circ_219808,RMVar_hsa_circ_105517,RMVar_hsa_circ_366230,RMVar_hsa_circ_300614,RMVar_hsa_circ_69022,RMVar_hsa_circ_219813,RMVar_hsa_circ_20894 14490 RMVar_ID_14490 Human_SNP_ID_140929853 A-to-I Human chr3 - 81524318 81524318 81524318 AAAAAATTTAATAATCTTATTTAAAAATGGGCAGAAGATCTGAATATACATCTCAAGAAGACATA AAAAAATTTAATAATCTTATTTAAAAATGGGCGGAAGATCTGAATATACATCTCAAGAAGACATA T C GBE1 Ensembl:ENSG00000114480 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1306075842 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85315,RMVar_hsa_circ_107938,RMVar_hsa_circ_124462,RMVar_hsa_circ_119461,RMVar_hsa_circ_100562,RMVar_hsa_circ_96350,RMVar_hsa_circ_22294,RMVar_hsa_circ_219807,RMVar_hsa_circ_219809,RMVar_hsa_circ_219811,RMVar_hsa_circ_219812,RMVar_hsa_circ_219810,RMVar_hsa_circ_219808,RMVar_hsa_circ_105517,RMVar_hsa_circ_366230,RMVar_hsa_circ_300614,RMVar_hsa_circ_69022,RMVar_hsa_circ_219813,RMVar_hsa_circ_20894 14491 RMVar_ID_14491 Human_SNP_ID_140929981 A-to-I Human chr3 - 81524774 81524773 81524774 AGTGACCAAAACAGCATGGTAATGCCATAAAAACAGACACAAATACCAGTAGAACAGAATATAAA AGTGACCAAAACAGCATGGTAATGCCATAAAA_CAGACACAAATACCAGTAGAACAGAATATAAA GT G GBE1 Ensembl:ENSG00000114480 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1451006392 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_85315,RMVar_hsa_circ_107938,RMVar_hsa_circ_124462,RMVar_hsa_circ_119461,RMVar_hsa_circ_100562,RMVar_hsa_circ_96350,RMVar_hsa_circ_22294,RMVar_hsa_circ_219807,RMVar_hsa_circ_219809,RMVar_hsa_circ_219811,RMVar_hsa_circ_219812,RMVar_hsa_circ_219810,RMVar_hsa_circ_219808,RMVar_hsa_circ_105517,RMVar_hsa_circ_366230,RMVar_hsa_circ_300614,RMVar_hsa_circ_69022,RMVar_hsa_circ_219813,RMVar_hsa_circ_20894 14492 RMVar_ID_14492 Human_SNP_ID_140940695 A-to-I Human chr3 - 81570675 81570675 81570675 TTATGAAGGCCTATAACATCCTTTATGATCCAACTACTGCCTACCTTTCCACCCAGATATCTCTG TTATGAAGGCCTATAACATCCTTTATGATCCATCTACTGCCTACCTTTCCACCCAGATATCTCTG T A GBE1 Ensembl:ENSG00000114480 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs928730578 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107938,RMVar_hsa_circ_124462,RMVar_hsa_circ_119461,RMVar_hsa_circ_100562,RMVar_hsa_circ_96350,RMVar_hsa_circ_22294,RMVar_hsa_circ_219809,RMVar_hsa_circ_219811,RMVar_hsa_circ_219812,RMVar_hsa_circ_219810,RMVar_hsa_circ_219808,RMVar_hsa_circ_105517,RMVar_hsa_circ_366230,RMVar_hsa_circ_69022,RMVar_hsa_circ_219813 14493 RMVar_ID_14493 Human_SNP_ID_140940696 A-to-I Human chr3 - 81570675 81570675 81570675 TTATGAAGGCCTATAACATCCTTTATGATCCAACTACTGCCTACCTTTCCACCCAGATATCTCTG TTATGAAGGCCTATAACATCCTTTATGATCCAGCTACTGCCTACCTTTCCACCCAGATATCTCTG T C GBE1 Ensembl:ENSG00000114480 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs928730578 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107938,RMVar_hsa_circ_124462,RMVar_hsa_circ_119461,RMVar_hsa_circ_100562,RMVar_hsa_circ_96350,RMVar_hsa_circ_22294,RMVar_hsa_circ_219809,RMVar_hsa_circ_219811,RMVar_hsa_circ_219812,RMVar_hsa_circ_219810,RMVar_hsa_circ_219808,RMVar_hsa_circ_105517,RMVar_hsa_circ_366230,RMVar_hsa_circ_69022,RMVar_hsa_circ_219813 14494 RMVar_ID_14494 Human_SNP_ID_140976378 A-to-I Human chr3 - 81723619 81723619 81723619 TGTTGCTGGAAGTAAGAAGAAAGAAGGAAAATAGGTATTGAAGCAAACAATAATAAAATAGATCG TGTTGCTGGAAGTAAGAAGAAAGAAGGAAAATTGGTATTGAAGCAAACAATAATAAAATAGATCG T A GBE1 Ensembl:ENSG00000114480 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1480705012 Functional Loss SNV dbSNP153 33..33 33 - - - 14495 RMVar_ID_14495 Human_SNP_ID_140976932 A-to-I Human chr3 - 81726408 81726407 81726408 TACACTGAGAGTCCCAGTGATAGATCTGTTTTATTACTGTTTGTTTCAATAACCATTTCCTGTCT TACACTGAGAGTCCCAGTGATAGATCTGTTTT_TTACTGTTTGTTTCAATAACCATTTCCTGTCT AT A GBE1 Ensembl:ENSG00000114480 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1182173622 Functional Loss DEL dbSNP153 33..33 33 - - - 14496 RMVar_ID_14496 Human_SNP_ID_140976933 A-to-I Human chr3 - 81726408 81726408 81726408 TACACTGAGAGTCCCAGTGATAGATCTGTTTTATTACTGTTTGTTTCAATAACCATTTCCTGTCT TACACTGAGAGTCCCAGTGATAGATCTGTTTTGTTACTGTTTGTTTCAATAACCATTTCCTGTCT T C GBE1 Ensembl:ENSG00000114480 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037213730 Functional Loss SNV dbSNP153 33..33 33 - - - 14497 RMVar_ID_14497 Human_SNP_ID_141837390 A-to-I Human chr3 + 85011855 85011855 85011855 CTGCATGCCACTGCACTACAACCGGGGTTACAAAGAAAGACCCTGTCTCAAAAAATAAATAAATA CTGCATGCCACTGCACTACAACCGGGGTTACAGAGAAAGACCCTGTCTCAAAAAATAAATAAATA A G CADM2 Ensembl:ENSG00000175161 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1465879887 Functional Loss SNV dbSNP153 33..33 33 - - - 14498 RMVar_ID_14498 Human_SNP_ID_141849375 A-to-I Human chr3 + 85060327 85060327 85060327 TTTTTGTATTTTTAGTAGAGACGGGTTTCACCAGGTTGGCCATGCTGGTCTCGAACTCCTGACCT TTTTTGTATTTTTAGTAGAGACGGGTTTCACCTGGTTGGCCATGCTGGTCTCGAACTCCTGACCT A T CADM2 Ensembl:ENSG00000175161 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1293914958 Functional Loss SNV dbSNP153 33..33 33 - - - 14499 RMVar_ID_14499 Human_SNP_ID_141864802 A-to-I Human chr3 + 85119286 85119286 85119286 AAATCCGGGCATTGTGACATACATGCGGACCTATAGTACCAGCTACCCCGGAGCCTGAGGTGGCA AAATCCGGGCATTGTGACATACATGCGGACCTGTAGTACCAGCTACCCCGGAGCCTGAGGTGGCA A G CADM2 Ensembl:ENSG00000175161 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1258013358 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9144984 14500 RMVar_ID_14500 Human_SNP_ID_141866500 A-to-I Human chr3 + 85125581 85125581 85125581 AGGGTTTTGCCATGTGGCCCACGCTGGTCTGGAAATCCTGAGCTCAAGGCATCCACCTGCCCTGG AGGGTTTTGCCATGTGGCCCACGCTGGTCTGGGAATCCTGAGCTCAAGGCATCCACCTGCCCTGG A G CADM2 Ensembl:ENSG00000175161 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1465737292 Functional Loss SNV dbSNP153 33..33 33 - - - 14501 RMVar_ID_14501 Human_SNP_ID_141878025 A-to-I Human chr3 + 85169693 85169693 85169693 ACCCAGGAGGCTGAGGCAGGAGAATTGCTTGTACCCTGGAGACGAAGGTTGCAGTGAGCGAGGTG ACCCAGGAGGCTGAGGCAGGAGAATTGCTTGTGCCCTGGAGACGAAGGTTGCAGTGAGCGAGGTG A G CADM2 Ensembl:ENSG00000175161 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1183318192 Functional Loss SNV dbSNP153 33..33 33 - - - 14502 RMVar_ID_14502 Human_SNP_ID_141878215 A-to-I Human chr3 + 85170468 85170468 85170468 TTTCGCGATTCTTCTGCCTCAATCTCCTGAGTAGCCAGGATTACAGGCGCCCGCCACCACGCCCG TTTCGCGATTCTTCTGCCTCAATCTCCTGAGTGGCCAGGATTACAGGCGCCCGCCACCACGCCCG A G CADM2 Ensembl:ENSG00000175161 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs931681180 Functional Loss SNV dbSNP153 33..33 33 - - - 14503 RMVar_ID_14503 Human_SNP_ID_141897736 A-to-I Human chr3 + 85248436 85248436 85248436 AGCTGGGATTACAGATGCACGCCACCAGGCCCAGCTAATTTGTTGTATTTTTACTAAAGAAGGGG AGCTGGGATTACAGATGCACGCCACCAGGCCCGGCTAATTTGTTGTATTTTTACTAAAGAAGGGG A G CADM2 Ensembl:ENSG00000175161 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1163043727 Functional Loss SNV dbSNP153 33..33 33 - - - 14504 RMVar_ID_14504 Human_SNP_ID_141919095 A-to-I Human chr3 + 85330851 85330851 85330851 GCACGGTGGTGTGTGTGCCTGTGGTTTCAGCTACTCAGGAGGCTGAGGTGGGAAGATTGTTTGAG GCACGGTGGTGTGTGTGCCTGTGGTTTCAGCTGCTCAGGAGGCTGAGGTGGGAAGATTGTTTGAG A G CADM2 Ensembl:ENSG00000175161 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1323839459 Functional Loss SNV dbSNP153 33..33 33 - - - 14505 RMVar_ID_14505 Human_SNP_ID_141919097 A-to-I Human chr3 + 85330855 85330855 85330855 GGTGGTGTGTGTGCCTGTGGTTTCAGCTACTCAGGAGGCTGAGGTGGGAAGATTGTTTGAGCCTG GGTGGTGTGTGTGCCTGTGGTTTCAGCTACTCCGGAGGCTGAGGTGGGAAGATTGTTTGAGCCTG A C CADM2 Ensembl:ENSG00000175161 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs902365406 Functional Loss SNV dbSNP153 33..33 33 - - - 14506 RMVar_ID_14506 Human_SNP_ID_141923510 A-to-I Human chr3 + 85347134 85347134 85347134 GATCCGAGCTACTCTGGAGGCTGATGCAGGAGAATACTTGAATCCAGCCGGCAGAGGTTTTGGTG GATCCGAGCTACTCTGGAGGCTGATGCAGGAGGATACTTGAATCCAGCCGGCAGAGGTTTTGGTG A G CADM2 Ensembl:ENSG00000175161 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1483994266 Functional Loss SNV dbSNP153 33..33 33 - - - 14507 RMVar_ID_14507 Human_SNP_ID_141929515 A-to-I Human chr3 + 85368105 85368105 85368105 TTATGGCCCCTTAGCAAAGATATCTTTCCAATAATTTTTCCAGTTACCAAGGCTATTATTAATTG TTATGGCCCCTTAGCAAAGATATCTTTCCAATCATTTTTCCAGTTACCAAGGCTATTATTAATTG A C CADM2 Ensembl:ENSG00000175161 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs977026151 Functional Loss SNV dbSNP153 33..33 33 - - - 14508 RMVar_ID_14508 Human_SNP_ID_141941225 A-to-I Human chr3 + 85411953 85411953 85411953 AGGTTCAAGCTATCCTTCTGCCTCAACCTCCCAAGTCACTGTGATTACACCCATATGCCACCATG AGGTTCAAGCTATCCTTCTGCCTCAACCTCCCTAGTCACTGTGATTACACCCATATGCCACCATG A T CADM2 Ensembl:ENSG00000175161 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1479544095 Functional Loss SNV dbSNP153 33..33 33 - - - 14509 RMVar_ID_14509 Human_SNP_ID_141950388 A-to-I Human chr3 + 85446658 85446658 85446658 GAGTTTCATTCTTGTTGCCCAGACTGGAGTACAAGGGTGCTATCTCAGCTCACCGCAACCTCCCC GAGTTTCATTCTTGTTGCCCAGACTGGAGTACGAGGGTGCTATCTCAGCTCACCGCAACCTCCCC A G CADM2 Ensembl:ENSG00000175161 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1352316122 Functional Loss SNV dbSNP153 33..33 33 - - - 14510 RMVar_ID_14510 Human_SNP_ID_142006632 A-to-I Human chr3 + 85657967 85657967 85657967 GATTGAACACACTAATTGATGCCATATTGTATATCTCTAATTTGTATGTGTTTGGTTTGGATTCA GATTGAACACACTAATTGATGCCATATTGTATGTCTCTAATTTGTATGTGTTTGGTTTGGATTCA A G CADM2 Ensembl:ENSG00000175161 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1430520738 Functional Loss SNV dbSNP153 33..33 33 - - - 14511 RMVar_ID_14511 Human_SNP_ID_142006661 A-to-I Human chr3 + 85658083 85658083 85658083 TGATGAGAATTTCAATTTAGAGTGATTGATTTAGTTAAGATATGTGGTTTGGATACAAGTAGGAA TGATGAGAATTTCAATTTAGAGTGATTGATTTGGTTAAGATATGTGGTTTGGATACAAGTAGGAA A G CADM2 Ensembl:ENSG00000175161 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1345179449 Functional Loss SNV dbSNP153 33..33 33 - - - 14512 RMVar_ID_14512 Human_SNP_ID_142645621 A-to-I Human chr3 - 88055483 88055483 88055483 ATATGAGAATGAGAATCAACTCCTCAACTCACAAGATTGTTGACTAGGAGGTTACCACCATTGTG ATATGAGAATGAGAATCAACTCCTCAACTCACTAGATTGTTGACTAGGAGGTTACCACCATTGTG T A CGGBP1 Ensembl:ENSG00000163320 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1488425035 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_608688,Human_RBP_ID_1034321,Human_RBP_ID_1632005,Human_RBP_ID_1969614,Human_RBP_ID_3718848,Human_RBP_ID_8124279,Human_RBP_ID_8874449,Human_RBP_ID_9146045,Human_RBP_ID_9261077,Human_RBP_ID_9302063,Human_RBP_ID_9393853,Human_RBP_ID_14953578,Human_RBP_ID_17290984,Human_RBP_ID_17404297,Human_RBP_ID_17521044,Human_RBP_ID_17704660,Human_RBP_ID_18011530,Human_RBP_ID_18341444,Human_RBP_ID_22423393,Human_RBP_ID_22509953,Human_RBP_ID_23287854,Human_RBP_ID_27059524,Human_RBP_ID_27721277 14513 RMVar_ID_14513 Human_SNP_ID_142669647 A-to-I Human chr3 + 88159447 88159447 88159447 ATAGTGGGCTGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGCGGA ATAGTGGGCTGGGCGCGGTGGCTCACGCCTGTCATCCCAGCACTTTGGGAGGCCGAGGCGGCGGA A C C3orf38 Ensembl:ENSG00000179021 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1201247034 Functional Loss SNV dbSNP153 33..33 33 - - - 14514 RMVar_ID_14514 Human_SNP_ID_142670217 A-to-I Human chr3 + 88161505 88161505 88161505 TCTGCCTCAGGCTCCCGAGTAGCTGGGTCTACAGGTGCGTGCCGCCATGCCTGGCTAATTTTTTT TCTGCCTCAGGCTCCCGAGTAGCTGGGTCTACGGGTGCGTGCCGCCATGCCTGGCTAATTTTTTT A G C3orf38 Ensembl:ENSG00000179021 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1434863247 Functional Loss SNV dbSNP153 33..33 33 - - - 14515 RMVar_ID_14515 Human_SNP_ID_142706668 A-to-I Human chr3 - 88318090 88318090 88318090 GTTCTCTCCTCCAGCTCTAGCCACATCTTCACATACTGATCATAATTACCCATAAAATACTTCAG GTTCTCTCCTCCAGCTCTAGCCACATCTTCACGTACTGATCATAATTACCCATAAAATACTTCAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878997718 Functional Loss SNV dbSNP153 33..33 33 - - - 14516 RMVar_ID_14516 Human_SNP_ID_237108695 A-to-I Human chr5 + 75344243 75344243 75344243 AAGTTTTTTTAGTATTGAACTTTTGTCATTTTAGGTATTGCTGGCCTTTTCACAATTTTCTCAAG AAGTTTTTTTAGTATTGAACTTTTGTCATTTTGGGTATTGCTGGCCTTTTCACAATTTTCTCAAG A G HMGCR Ensembl:ENSG00000113161 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1205490780 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_944356,Human_RBP_ID_1322711 Human_Splice_Rec_663117,Human_Splice_Rec_663155,Human_Splice_Rec_663193 RMVar_hsa_circ_46758,RMVar_hsa_circ_21355,RMVar_hsa_circ_106546,RMVar_hsa_circ_109552,RMVar_hsa_circ_124528,RMVar_hsa_circ_265315,RMVar_hsa_circ_232512,RMVar_hsa_circ_309161,RMVar_hsa_circ_115051,RMVar_hsa_circ_67534,RMVar_hsa_circ_69658,RMVar_hsa_circ_64190,RMVar_hsa_circ_232513,RMVar_hsa_circ_232515,RMVar_hsa_circ_232516,RMVar_hsa_circ_232514,RMVar_hsa_circ_273068,RMVar_hsa_circ_278717,RMVar_hsa_circ_302817,RMVar_hsa_circ_100213,RMVar_hsa_circ_9032,RMVar_hsa_circ_97703,RMVar_hsa_circ_232517,RMVar_hsa_circ_232519,RMVar_hsa_circ_232520,RMVar_hsa_circ_232518,RMVar_hsa_circ_121690,RMVar_hsa_circ_63485 14517 RMVar_ID_14517 Human_SNP_ID_237109153 A-to-I Human chr5 + 75346266 75346266 75346266 TAATTTCTGACCTCAAGTGATCCACCCGCCTCAGCCTCCCAAAGTGGTGGGATTATAGGTGTGAG TAATTTCTGACCTCAAGTGATCCACCCGCCTCGGCCTCCCAAAGTGGTGGGATTATAGGTGTGAG A G HMGCR Ensembl:ENSG00000113161 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs192517674 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_46758,RMVar_hsa_circ_109552,RMVar_hsa_circ_124528,RMVar_hsa_circ_265315,RMVar_hsa_circ_232512,RMVar_hsa_circ_309161,RMVar_hsa_circ_115051,RMVar_hsa_circ_67534,RMVar_hsa_circ_69658,RMVar_hsa_circ_64190,RMVar_hsa_circ_232513,RMVar_hsa_circ_232515,RMVar_hsa_circ_232514,RMVar_hsa_circ_273068,RMVar_hsa_circ_100213,RMVar_hsa_circ_9032,RMVar_hsa_circ_97703,RMVar_hsa_circ_232519,RMVar_hsa_circ_232520,RMVar_hsa_circ_63485,RMVar_hsa_circ_232522,RMVar_hsa_circ_108060,RMVar_hsa_circ_232523 14518 RMVar_ID_14518 Human_SNP_ID_237117077 A-to-I Human chr5 - 75377997 75377997 75377997 AGGTGGGAGAATGGCTTGAGGCCAGGAGTTCAAGTCTAGCCTGGATAACATAGCAAGATTCCATC AGGTGGGAGAATGGCTTGAGGCCAGGAGTTCAGGTCTAGCCTGGATAACATAGCAAGATTCCATC T C CERT1 Ensembl:ENSG00000113163 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs775637134 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269711 14519 RMVar_ID_14519 Human_SNP_ID_237117087 A-to-I Human chr5 - 75378047 75378047 75378047 GCCAGGTGCAGTGGGTCACACCTGTAATCCCAACACTTTTTGGGAGACTGAGGTGGGAGAATGGC GCCAGGTGCAGTGGGTCACACCTGTAATCCCAGCACTTTTTGGGAGACTGAGGTGGGAGAATGGC T C CERT1 Ensembl:ENSG00000113163 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs963099315 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269711 14520 RMVar_ID_14520 Human_SNP_ID_237117088 A-to-I Human chr5 - 75378053 75378053 75378053 AAAGTGGCCAGGTGCAGTGGGTCACACCTGTAATCCCAACACTTTTTGGGAGACTGAGGTGGGAG AAAGTGGCCAGGTGCAGTGGGTCACACCTGTAGTCCCAACACTTTTTGGGAGACTGAGGTGGGAG T C CERT1 Ensembl:ENSG00000113163 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs946794528 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269711 14521 RMVar_ID_14521 Human_SNP_ID_237117169 A-to-I Human chr5 - 75378373 75378373 75378373 TCTTGCTGCCCAGGCTGGAGTGCAGTGGTGCAATCTTGGCTCACTGCAACCTCTGCCTCCCAGGT TCTTGCTGCCCAGGCTGGAGTGCAGTGGTGCAGTCTTGGCTCACTGCAACCTCTGCCTCCCAGGT T C CERT1 Ensembl:ENSG00000113163 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1018840206 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_166754 RMVar_hsa_circ_269711 14522 RMVar_ID_14522 Human_SNP_ID_237117309 A-to-I Human chr5 - 75378957 75378957 75378957 CCAAGCTGGTCTTGAACTCCTGGCCTCAGACAATCCTCCTGCCTCAGCCTCCCAAAGTGCTGGGA CCAAGCTGGTCTTGAACTCCTGGCCTCAGACAGTCCTCCTGCCTCAGCCTCCCAAAGTGCTGGGA T C CERT1 Ensembl:ENSG00000113163 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs555727983 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269711 14523 RMVar_ID_14523 Human_SNP_ID_237117357 A-to-I Human chr5 - 75379143 75379143 75379143 GGGTCTTGCTCTGTTTCCTAAGCTGAAGTGCAATGACACCATCACGGCTCACTGCAACCTCAACC GGGTCTTGCTCTGTTTCCTAAGCTGAAGTGCAGTGACACCATCACGGCTCACTGCAACCTCAACC T C CERT1 Ensembl:ENSG00000113163 Protein coding intron GSE38233;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;ASD brains,cerebellum;Bronchiolar epithelium,BEP2D cell line - 24183664,30559470,31158229 RNA-Seq:(High) rs1040135463 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17630792,Human_RBP_ID_19127248 RMVar_hsa_circ_269711 14524 RMVar_ID_14524 Human_SNP_ID_237124330 A-to-I Human chr5 - 75406609 75406609 75406609 CTTGAACCGGCAGGCGGAAGCTGCAGTGAGCCAAGACCTCGCTACTGCACTCCAGCCTGGGCAAC CTTGAACCGGCAGGCGGAAGCTGCAGTGAGCCCAGACCTCGCTACTGCACTCCAGCCTGGGCAAC T G CERT1 Ensembl:ENSG00000113163 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1182800291 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5320,RMVar_hsa_circ_269711,RMVar_hsa_circ_359059,RMVar_hsa_circ_304342,RMVar_hsa_circ_50831,RMVar_hsa_circ_48425,RMVar_hsa_circ_232536,RMVar_hsa_circ_312241,RMVar_hsa_circ_369184,RMVar_hsa_circ_56449,RMVar_hsa_circ_232539,RMVar_hsa_circ_232538,RMVar_hsa_circ_339008,RMVar_hsa_circ_127187,RMVar_hsa_circ_232540,RMVar_hsa_circ_232541,RMVar_hsa_circ_20869,RMVar_hsa_circ_36495,RMVar_hsa_circ_232544,RMVar_hsa_circ_32544,RMVar_hsa_circ_64928,RMVar_hsa_circ_330323,RMVar_hsa_circ_45936,RMVar_hsa_circ_318181,RMVar_hsa_circ_344124,RMVar_hsa_circ_232545,RMVar_hsa_circ_357061,RMVar_hsa_circ_275991,RMVar_hsa_circ_232548,RMVar_hsa_circ_232546,RMVar_hsa_circ_232547,RMVar_hsa_circ_277707 14525 RMVar_ID_14525 Human_SNP_ID_237125172 A-to-I Human chr5 - 75409733 75409733 75409733 CACAAGGTCAAGAGCTCGAGACCAGCCTGGCCAATATGGTGAAACCCCGTCTCTACTAAAAAAAT CACAAGGTCAAGAGCTCGAGACCAGCCTGGCCGATATGGTGAAACCCCGTCTCTACTAAAAAAAT T C CERT1 Ensembl:ENSG00000113163 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs963791317 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5320,RMVar_hsa_circ_269711,RMVar_hsa_circ_359059,RMVar_hsa_circ_304342,RMVar_hsa_circ_50831,RMVar_hsa_circ_48425,RMVar_hsa_circ_232536,RMVar_hsa_circ_312241,RMVar_hsa_circ_369184,RMVar_hsa_circ_56449,RMVar_hsa_circ_232539,RMVar_hsa_circ_232538,RMVar_hsa_circ_339008,RMVar_hsa_circ_127187,RMVar_hsa_circ_232540,RMVar_hsa_circ_232541,RMVar_hsa_circ_20869,RMVar_hsa_circ_36495,RMVar_hsa_circ_232544,RMVar_hsa_circ_32544,RMVar_hsa_circ_64928,RMVar_hsa_circ_330323,RMVar_hsa_circ_45936,RMVar_hsa_circ_318181,RMVar_hsa_circ_344124,RMVar_hsa_circ_232545,RMVar_hsa_circ_357061,RMVar_hsa_circ_275991,RMVar_hsa_circ_232548,RMVar_hsa_circ_232546,RMVar_hsa_circ_232547,RMVar_hsa_circ_277707 14526 RMVar_ID_14526 Human_SNP_ID_237125276 A-to-I Human chr5 - 75410004 75410004 75410004 GGCCAGGAGTTCAAGACCAACCTGGACAGCATAGCAAGACTTCATCTCTATAAAATAAAATAACA GGCCAGGAGTTCAAGACCAACCTGGACAGCATGGCAAGACTTCATCTCTATAAAATAAAATAACA T C CERT1 Ensembl:ENSG00000113163 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1221308863 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5320,RMVar_hsa_circ_269711,RMVar_hsa_circ_359059,RMVar_hsa_circ_304342,RMVar_hsa_circ_50831,RMVar_hsa_circ_48425,RMVar_hsa_circ_232536,RMVar_hsa_circ_312241,RMVar_hsa_circ_369184,RMVar_hsa_circ_56449,RMVar_hsa_circ_232539,RMVar_hsa_circ_232538,RMVar_hsa_circ_339008,RMVar_hsa_circ_127187,RMVar_hsa_circ_232540,RMVar_hsa_circ_232541,RMVar_hsa_circ_20869,RMVar_hsa_circ_36495,RMVar_hsa_circ_232544,RMVar_hsa_circ_32544,RMVar_hsa_circ_64928,RMVar_hsa_circ_330323,RMVar_hsa_circ_45936,RMVar_hsa_circ_318181,RMVar_hsa_circ_344124,RMVar_hsa_circ_232545,RMVar_hsa_circ_357061,RMVar_hsa_circ_275991,RMVar_hsa_circ_232548,RMVar_hsa_circ_232546,RMVar_hsa_circ_232547,RMVar_hsa_circ_277707 14527 RMVar_ID_14527 Human_SNP_ID_237151944 A-to-I Human chr5 + 75516373 75516373 75516373 TGGGAGGCTGAGGCAGAGGATTGCTTGACCCCAGGAGTTTCAGACCAGTCTGGGCAACATAGGGA TGGGAGGCTGAGGCAGAGGATTGCTTGACCCCGGGAGTTTCAGACCAGTCTGGGCAACATAGGGA A G POLK Ensembl:ENSG00000122008 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs989986942 Functional Loss SNV dbSNP153 33..33 33 - - - 14528 RMVar_ID_14528 Human_SNP_ID_237157490 A-to-I Human chr5 + 75540488 75540488 75540488 GTCAACACACCTGGCTATTTTTTTGTGTAGACAGGGTCTCACTATGTTGCCCAGGCTGGTCTTGA GTCAACACACCTGGCTATTTTTTTGTGTAGACTGGGTCTCACTATGTTGCCCAGGCTGGTCTTGA A T POLK Ensembl:ENSG00000122008 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs998897034 Functional Loss SNV dbSNP153 33..33 33 - - - 14529 RMVar_ID_14529 Human_SNP_ID_237158181 A-to-I Human chr5 + 75543260 75543259 75543260 GAGGGTTTCACCATTTTGGCCAGGTTGGTCTCAAACTCCTGATTTCAGGTGATCCACCCACCTCG GAGGGTTTCACCATTTTGGCCAGGTTGGTCTC_AACTCCTGATTTCAGGTGATCCACCCACCTCG CA C POLK Ensembl:ENSG00000122008 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1342889323 Functional Loss DEL dbSNP153 33..33 33 - - - 14530 RMVar_ID_14530 Human_SNP_ID_237158182 A-to-I Human chr5 + 75543260 75543260 75543260 GAGGGTTTCACCATTTTGGCCAGGTTGGTCTCAAACTCCTGATTTCAGGTGATCCACCCACCTCG GAGGGTTTCACCATTTTGGCCAGGTTGGTCTCGAACTCCTGATTTCAGGTGATCCACCCACCTCG A G POLK Ensembl:ENSG00000122008 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1452994916 Functional Loss SNV dbSNP153 33..33 33 - - - 14531 RMVar_ID_14531 Human_SNP_ID_237158453 A-to-I Human chr5 + 75544458 75544458 75544458 CACTTGAGTAGTTTGAGACCAGCCTGGCTAACATGACGAAACCCCATCTTTACTAAAAATACAAA CACTTGAGTAGTTTGAGACCAGCCTGGCTAACGTGACGAAACCCCATCTTTACTAAAAATACAAA A G POLK Ensembl:ENSG00000122008 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs763292889 Functional Loss SNV dbSNP153 33..33 33 - - - 14532 RMVar_ID_14532 Human_SNP_ID_237158454 A-to-I Human chr5 + 75544458 75544458 75544458 CACTTGAGTAGTTTGAGACCAGCCTGGCTAACATGACGAAACCCCATCTTTACTAAAAATACAAA CACTTGAGTAGTTTGAGACCAGCCTGGCTAACTTGACGAAACCCCATCTTTACTAAAAATACAAA A T POLK Ensembl:ENSG00000122008 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs763292889 Functional Loss SNV dbSNP153 33..33 33 - - - 14533 RMVar_ID_14533 Human_SNP_ID_237159036 A-to-I Human chr5 + 75546935 75546935 75546935 TCAATCTGCCCGCCTCGGCCTCCCAAAGTGCTAGGATTACGGGCATGAGCCACCACGCCTGGCCA TCAATCTGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACGGGCATGAGCCACCACGCCTGGCCA A G POLK Ensembl:ENSG00000122008 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs567231277 Functional Loss SNV dbSNP153 33..33 33 - - - 14534 RMVar_ID_14534 Human_SNP_ID_237167030 A-to-I Human chr5 + 75582738 75582738 75582738 GGGAGGCCGAAGCTCGTGGACTACCTGAGGTCAGGAGTTCGAGACCAGCCTGACCAATATGGTGA GGGAGGCCGAAGCTCGTGGACTACCTGAGGTCGGGAGTTCGAGACCAGCCTGACCAATATGGTGA A G POLK Ensembl:ENSG00000122008 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1325286940 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9090,RMVar_hsa_circ_335745,RMVar_hsa_circ_344649,RMVar_hsa_circ_70582,RMVar_hsa_circ_25181,RMVar_hsa_circ_49008,RMVar_hsa_circ_232555,RMVar_hsa_circ_232554,RMVar_hsa_circ_42682,RMVar_hsa_circ_37873,RMVar_hsa_circ_40894,RMVar_hsa_circ_31385,RMVar_hsa_circ_48801,RMVar_hsa_circ_232558,RMVar_hsa_circ_232559,RMVar_hsa_circ_31421,RMVar_hsa_circ_363145,RMVar_hsa_circ_16965,RMVar_hsa_circ_71111 14535 RMVar_ID_14535 Human_SNP_ID_237168639 A-to-I Human chr5 + 75589525 75589525 75589525 CAGGCTGGAGTGCAGTGGTGCGATCTCGGTTCACTGCAAGCTCCGCCTCCTGGGTTCTCGCCATT CAGGCTGGAGTGCAGTGGTGCGATCTCGGTTCGCTGCAAGCTCCGCCTCCTGGGTTCTCGCCATT A G POLK Ensembl:ENSG00000122008 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1287934550 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9090,RMVar_hsa_circ_335745,RMVar_hsa_circ_232554,RMVar_hsa_circ_42682,RMVar_hsa_circ_37873,RMVar_hsa_circ_40894,RMVar_hsa_circ_48801,RMVar_hsa_circ_232558,RMVar_hsa_circ_232559,RMVar_hsa_circ_16965,RMVar_hsa_circ_19824,RMVar_hsa_circ_29797,RMVar_hsa_circ_232560 14536 RMVar_ID_14536 Human_SNP_ID_237169478 A-to-I Human chr5 + 75593332 75593332 75593332 TTTTGTATTTTTATTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGACCT TTTTGTATTTTTATTAGAGACAGGGTTTCACCGTGTTGGCCAGGCTGGTCTTGAACTCCTGACCT A G POLK Ensembl:ENSG00000122008 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1462867529 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9090,RMVar_hsa_circ_40894,RMVar_hsa_circ_232559,RMVar_hsa_circ_29797,RMVar_hsa_circ_14023 14537 RMVar_ID_14537 Human_SNP_ID_237169549 A-to-I Human chr5 + 75593637 75593637 75593637 ACTTTGGGAGGCCAGGATCGCTTGTGGCCAGGAATTTGAGACTAGCCTGGGTAACATAGTGAGAC ACTTTGGGAGGCCAGGATCGCTTGTGGCCAGGGATTTGAGACTAGCCTGGGTAACATAGTGAGAC A G POLK Ensembl:ENSG00000122008 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1447217959 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25917883 RMVar_hsa_circ_9090,RMVar_hsa_circ_40894,RMVar_hsa_circ_232559,RMVar_hsa_circ_29797,RMVar_hsa_circ_14023 14538 RMVar_ID_14538 Human_SNP_ID_237171002 A-to-I Human chr5 + 75599172 75599172 75599172 TACTCAGATGGCTGAGGCAGGAGAACTACTTGAACCTGGGAGGTCAAAGCTGCAGTCAGCCAAGA TACTCAGATGGCTGAGGCAGGAGAACTACTTGGACCTGGGAGGTCAAAGCTGCAGTCAGCCAAGA A G POLK Ensembl:ENSG00000122008 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1339846848 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_646471,Human_RBP_ID_15515150 Human_miRNA_ID_198317,Human_miRNA_ID_699000,Human_miRNA_ID_703923,Human_miRNA_ID_1464231 RMVar_hsa_circ_232561 14539 RMVar_ID_14539 Human_SNP_ID_237179586 A-to-I Human chr5 + 75637018 75637018 75637018 CCTATAATGCCAGCAGTTTGGGCGGCCGAGGTAGGCGGATCATCTGAGGTCAGGAGTTTGAGACC CCTATAATGCCAGCAGTTTGGGCGGCCGAGGTTGGCGGATCATCTGAGGTCAGGAGTTTGAGACC A T ANKDD1B Ensembl:ENSG00000189045 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1324579211 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11174 14540 RMVar_ID_14540 Human_SNP_ID_237331071 A-to-I Human chr5 + 76242305 76242305 76242305 CCTTCAGCCTTTCTCTTGGGCATGGTGGCGGCAGCGACGGCAGCGGGACATAGGTGCTGGACGCG CCTTCAGCCTTTCTCTTGGGCATGGTGGCGGCGGCGACGGCAGCGGGACATAGGTGCTGGACGCG A G SV2C Ensembl:ENSG00000122012 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878971128 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95491,RMVar_hsa_circ_344778,RMVar_hsa_circ_232574,RMVar_hsa_circ_81833,RMVar_hsa_circ_232575,RMVar_hsa_circ_232573 14541 RMVar_ID_14541 Human_SNP_ID_237364268 A-to-I Human chr5 + 76376899 76376899 76376899 GCTCCATTCTCTGCTCCTCCTCCTGTAGGAGCAATGATACCACCTCCCCCTAGTCTTCCAGGTCC GCTCCATTCTCTGCTCCTCCTCCTGTAGGAGCGATGATACCACCTCCCCCTAGTCTTCCAGGTCC A G SNRPCP2 Ensembl:ENSG00000251235 Pseudogene exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs562199453 Functional Loss SNV dbSNP153 33..33 33 - - - 14542 RMVar_ID_14542 Human_SNP_ID_237503801 A-to-I Human chr5 + 76956507 76956507 76956507 CCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGCGGATCACGAGGTCAGGAGATCCAGACCGT CCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGCGGATCACGAGGTCAGGAGATCCAGACCGT A G CRHBP Ensembl:ENSG00000145708 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1378827433 Functional Loss SNV dbSNP153 33..33 33 - - - 14543 RMVar_ID_14543 Human_SNP_ID_237503818 A-to-I Human chr5 + 76956552 76956552 76956552 GGTCAGGAGATCCAGACCGTCCTGGCTAACACAGTGAAACCCCATCTCTACTAAAAATGCAAAAA GGTCAGGAGATCCAGACCGTCCTGGCTAACACCGTGAAACCCCATCTCTACTAAAAATGCAAAAA A C CRHBP Ensembl:ENSG00000145708 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1265583279 Functional Loss SNV dbSNP153 33..33 33 - - - 14544 RMVar_ID_14544 Human_SNP_ID_237524492 A-to-I Human chr5 + 77040384 77040384 77040384 CTCCTGCCTCTGCCTCCCAAAGTGCTGAGATTACAGGCATGAGCCACCGCACCCGGCCAGGAAAA CTCCTGCCTCTGCCTCCCAAAGTGCTGAGATTGCAGGCATGAGCCACCGCACCCGGCCAGGAAAA A G AC008581.2,AGGF1 Ensembl:ENSG00000285000,Ensembl:ENSG00000164252 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1293818673 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33180,RMVar_hsa_circ_232594,RMVar_hsa_circ_277996,RMVar_hsa_circ_277430,RMVar_hsa_circ_58852,RMVar_hsa_circ_232596,RMVar_hsa_circ_232597,RMVar_hsa_circ_232595,RMVar_hsa_circ_49082,RMVar_hsa_circ_81165,RMVar_hsa_circ_232601,RMVar_hsa_circ_232603,RMVar_hsa_circ_232602,RMVar_hsa_circ_81813,RMVar_hsa_circ_307916,RMVar_hsa_circ_329231,RMVar_hsa_circ_232604 14545 RMVar_ID_14545 Human_SNP_ID_237526440 A-to-I Human chr5 + 77044944 77044944 77044944 AATTACCTGGGTATGGTGGTGCGCATGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGTAGA AATTACCTGGGTATGGTGGTGCGCATGCCTGTGGTCCCAGCTACTCGGGAGGCTGAGGCAGTAGA A G AC008581.2,AGGF1 Ensembl:ENSG00000285000,Ensembl:ENSG00000164252 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1247617444 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_165616 RMVar_hsa_circ_33180,RMVar_hsa_circ_232594,RMVar_hsa_circ_277996,RMVar_hsa_circ_277430,RMVar_hsa_circ_58852,RMVar_hsa_circ_232596,RMVar_hsa_circ_232597,RMVar_hsa_circ_232595,RMVar_hsa_circ_49082,RMVar_hsa_circ_81165,RMVar_hsa_circ_232601,RMVar_hsa_circ_232603,RMVar_hsa_circ_232602,RMVar_hsa_circ_81813,RMVar_hsa_circ_307916,RMVar_hsa_circ_329231,RMVar_hsa_circ_232604 14546 RMVar_ID_14546 Human_SNP_ID_237527720 A-to-I Human chr5 + 77049603 77049602 77049604 ATAGGATTTCACTCTGTTACCCAGGCTGGAGTACAGTGATGTGATCACGACTCACTGCAGCCTCA ATAGGATTTCACTCTGTTACCCAGGCTGGAGT__AGTGATGTGATCACGACTCACTGCAGCCTCA TAC T AC008581.2,AGGF1 Ensembl:ENSG00000285000,Ensembl:ENSG00000164252 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992158190 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_58852,RMVar_hsa_circ_57694,RMVar_hsa_circ_49082,RMVar_hsa_circ_349857,RMVar_hsa_circ_67259,RMVar_hsa_circ_109461,RMVar_hsa_circ_232610,RMVar_hsa_circ_232609,RMVar_hsa_circ_58599,RMVar_hsa_circ_287490 14547 RMVar_ID_14547 Human_SNP_ID_237537430 A-to-I Human chr5 + 77090020 77090020 77090020 GCAACATGCAGGGAACTAGAGGCCATCTTGTTAAGTGAAATAAATCAGACACAGAAAGGCAAAAA GCAACATGCAGGGAACTAGAGGCCATCTTGTTCAGTGAAATAAATCAGACACAGAAAGGCAAAAA A C AC008581.2,ZBED3-AS1,AC022414.1 Ensembl:ENSG00000285000,Ensembl:ENSG00000250802,Ensembl:ENSG00000284762 Protein coding,lincRNA,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1393146381 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_368770 14548 RMVar_ID_14548 Human_SNP_ID_237537432 A-to-I Human chr5 + 77090042 77090042 77090042 CCATCTTGTTAAGTGAAATAAATCAGACACAGAAAGGCAAAAATCACATGTTCACACTCATATGT CCATCTTGTTAAGTGAAATAAATCAGACACAGGAAGGCAAAAATCACATGTTCACACTCATATGT A G AC008581.2,ZBED3-AS1,AC022414.1 Ensembl:ENSG00000285000,Ensembl:ENSG00000250802,Ensembl:ENSG00000284762 Protein coding,lincRNA,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1374711724 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_368770 14549 RMVar_ID_14549 Human_SNP_ID_237539574 A-to-I Human chr5 + 77098733 77098733 77098733 CTACAGTTCTGGAGCCTTGGAAGTCCGAGATCAAGGAGCTGCATCTGGTGAGAGCCTTTTTGCAT CTACAGTTCTGGAGCCTTGGAAGTCCGAGATCTAGGAGCTGCATCTGGTGAGAGCCTTTTTGCAT A T AC008581.2,ZBED3-AS1,AC022414.1 Ensembl:ENSG00000285000,Ensembl:ENSG00000250802,Ensembl:ENSG00000284762 Protein coding,lincRNA,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1294649682 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_665238,Human_Splice_Rec_665239,Human_Splice_Rec_665246,Human_Splice_Rec_665247,Human_Splice_Rec_665256,Human_Splice_Rec_665257,Human_Splice_Rec_665268,Human_Splice_Rec_665269,Human_Splice_Rec_665296,Human_Splice_Rec_665297,Human_Splice_Rec_665306,Human_Splice_Rec_665307,Human_Splice_Rec_665324,Human_Splice_Rec_665325,Human_Splice_Rec_665332,Human_Splice_Rec_665333,Human_Splice_Rec_665346,Human_Splice_Rec_665352,Human_Splice_Rec_665353,Human_Splice_Rec_665380,Human_Splice_Rec_665381,Human_Splice_Rec_665390,Human_Splice_Rec_665391,Human_Splice_Rec_665400,Human_Splice_Rec_665401,Human_Splice_Rec_665418,Human_Splice_Rec_665419,Human_Splice_Rec_665424,Human_Splice_Rec_665425,Human_Splice_Rec_665436,Human_Splice_Rec_665437,Human_Splice_Rec_665444,Human_Splice_Rec_665445,Human_Splice_Rec_665452,Human_Splice_Rec_665453,Human_Splice_Rec_665464,Human_Splice_Rec_665465,Human_Splice_Rec_665474,Human_Splice_Rec_665475,Human_Splice_Rec_665490,Human_Splice_Rec_665491 RMVar_hsa_circ_232613,RMVar_hsa_circ_309052,RMVar_hsa_circ_368770,RMVar_hsa_circ_274563,RMVar_hsa_circ_232612 14550 RMVar_ID_14550 Human_SNP_ID_237615739 A-to-I Human chr5 - 77432511 77432511 77432511 GTGTGTTTTTCCCAGTGTGAATTGGCTTGAAGAGCCATGGGCTAAATGGGTACTAGAACAACAAC GTGTGTTTTTCCCAGTGTGAATTGGCTTGAAGTGCCATGGGCTAAATGGGTACTAGAACAACAAC T A WDR41 Ensembl:ENSG00000164253 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285782036 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_646732,Human_RBP_ID_15517310,Human_RBP_ID_23214474,Human_RBP_ID_24116681 Human_miRNA_ID_258943,Human_miRNA_ID_262737,Human_miRNA_ID_2986536 RMVar_hsa_circ_100994,RMVar_hsa_circ_119304,RMVar_hsa_circ_232620,RMVar_hsa_circ_98079,RMVar_hsa_circ_232621,RMVar_hsa_circ_232619 14551 RMVar_ID_14551 Human_SNP_ID_237615813 A-to-I Human chr5 + 77432726 77432726 77432726 AGTTTGTGCTATATAGAACACTAACAGTTACTAAAGACTAGGAAAATTTGCAGGAGAAAGGCTAT AGTTTGTGCTATATAGAACACTAACAGTTACTTAAGACTAGGAAAATTTGCAGGAGAAAGGCTAT A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1009860976 Functional Loss SNV dbSNP153 33..33 33 - - - 14552 RMVar_ID_14552 Human_SNP_ID_237615904 A-to-I Human chr5 - 77433022 77433022 77433022 TCACTTAAATTGGTAATTTTTTTTGTCAGTCCATAAAATTCTACATGTTTAAATTTTTTGTGGAC TCACTTAAATTGGTAATTTTTTTTGTCAGTCCTTAAAATTCTACATGTTTAAATTTTTTGTGGAC T A WDR41 Ensembl:ENSG00000164253 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs963421185 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_130932,Human_miRNA_ID_132215,Human_miRNA_ID_1980279,Human_miRNA_ID_1982005 RMVar_hsa_circ_100994,RMVar_hsa_circ_119304,RMVar_hsa_circ_51439,RMVar_hsa_circ_232620,RMVar_hsa_circ_98079,RMVar_hsa_circ_232621,RMVar_hsa_circ_340203,RMVar_hsa_circ_232619,RMVar_hsa_circ_287581,RMVar_hsa_circ_232622 14553 RMVar_ID_14553 Human_SNP_ID_237615905 A-to-I Human chr5 - 77433022 77433022 77433022 TCACTTAAATTGGTAATTTTTTTTGTCAGTCCATAAAATTCTACATGTTTAAATTTTTTGTGGAC TCACTTAAATTGGTAATTTTTTTTGTCAGTCCGTAAAATTCTACATGTTTAAATTTTTTGTGGAC T C WDR41 Ensembl:ENSG00000164253 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs963421185 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_130932,Human_miRNA_ID_132215,Human_miRNA_ID_1980279,Human_miRNA_ID_1982005 RMVar_hsa_circ_100994,RMVar_hsa_circ_119304,RMVar_hsa_circ_51439,RMVar_hsa_circ_232620,RMVar_hsa_circ_98079,RMVar_hsa_circ_232621,RMVar_hsa_circ_340203,RMVar_hsa_circ_232619,RMVar_hsa_circ_287581,RMVar_hsa_circ_232622 14554 RMVar_ID_14554 Human_SNP_ID_237618986 A-to-I Human chr5 - 77443989 77443989 77443989 GTAGTCCCAGCTACACAGGAGGCTGAGACAGGAATTGCTTGAACTTGGGAGGTGGAGGTTACAGG GTAGTCCCAGCTACACAGGAGGCTGAGACAGGGATTGCTTGAACTTGGGAGGTGGAGGTTACAGG T C WDR41 Ensembl:ENSG00000164253 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215706407 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40439,RMVar_hsa_circ_119304,RMVar_hsa_circ_232620,RMVar_hsa_circ_98079,RMVar_hsa_circ_232621,RMVar_hsa_circ_340203,RMVar_hsa_circ_287581,RMVar_hsa_circ_61154,RMVar_hsa_circ_232622,RMVar_hsa_circ_55821,RMVar_hsa_circ_266254,RMVar_hsa_circ_359418 14555 RMVar_ID_14555 Human_SNP_ID_237619005 A-to-I Human chr5 - 77444073 77444065 77444074 GAGTTTGAGACCAGCCTGGCCAACATGGCGAAACCCGTCACTACTAAAAATACAAAAATTAGCCA GAGTTTGAGACCAGCCTGGCCAACATGGCGA_________CTACTAAAAATACAAAAATTAGCCA GTGACGGGTT G WDR41 Ensembl:ENSG00000164253 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1415232144 Functional Loss DEL dbSNP153 32..40 33 - - - RMVar_hsa_circ_40439,RMVar_hsa_circ_119304,RMVar_hsa_circ_232620,RMVar_hsa_circ_98079,RMVar_hsa_circ_232621,RMVar_hsa_circ_340203,RMVar_hsa_circ_287581,RMVar_hsa_circ_61154,RMVar_hsa_circ_232622,RMVar_hsa_circ_55821,RMVar_hsa_circ_266254,RMVar_hsa_circ_359418 14556 RMVar_ID_14556 Human_SNP_ID_237631583 A-to-I Human chr5 - 77492197 77492197 77492197 GCTGCCCGGATGTTGCGATGGCTGATCGGGGGAGGCCGAGAACCGCAGGGACTGGCCGAGGTAAA GCTGCCCGGATGTTGCGATGGCTGATCGGGGGCGGCCGAGAACCGCAGGGACTGGCCGAGGTAAA T G WDR41 Ensembl:ENSG00000164253 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs773674090 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250304,Human_RBP_ID_788243,Human_RBP_ID_4845790,Human_RBP_ID_22458867,Human_RBP_ID_24116796 Human_Splice_Rec_665821,Human_Splice_Rec_665857,Human_Splice_Rec_665877,Human_Splice_Rec_665905,Human_Splice_Rec_665915,Human_Splice_Rec_665933,Human_Splice_Rec_665939,Human_Splice_Rec_665953,Human_Splice_Rec_665965,Human_Splice_Rec_665979,Human_Splice_Rec_665991,Human_Splice_Rec_666003,Human_Splice_Rec_666015,Human_Splice_Rec_666027,Human_Splice_Rec_666039,Human_Splice_Rec_666071,Human_Splice_Rec_666083,Human_Splice_Rec_666111 Human_miRNA_ID_2210084 RMVar_hsa_circ_124890,RMVar_hsa_circ_232623 14557 RMVar_ID_14557 Human_SNP_ID_237691282 A-to-I Human chr5 - 77746232 77746232 77746232 TAGAGACGGGGCCTCAATATGTTGCCCAGTCTAGTCTGGAACTCCTGAGCGTAAGTGATGCTTCT TAGAGACGGGGCCTCAATATGTTGCCCAGTCTCGTCTGGAACTCCTGAGCGTAAGTGATGCTTCT T G TBCA Ensembl:ENSG00000171530 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1230239561 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15519773 14558 RMVar_ID_14558 Human_SNP_ID_237693290 A-to-I Human chr5 - 77754002 77754002 77754002 CCTGTAATCCCAGCATTTTGGGAGGTCAAGGTAGGTAGATCACTTGAAGTCAGGAGTTCGAGACC CCTGTAATCCCAGCATTTTGGGAGGTCAAGGTGGGTAGATCACTTGAAGTCAGGAGTTCGAGACC T C TBCA Ensembl:ENSG00000171530 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs781150901 Functional Loss SNV dbSNP153 33..33 33 - - - 14559 RMVar_ID_14559 Human_SNP_ID_237693690 A-to-I Human chr5 - 77755808 77755808 77755808 TAGAGACAGGGTTTTTCCATGTTGGTTATGCTAGTCTCAAATTCCGAACTTCAGGTGATCTGCCC TAGAGACAGGGTTTTTCCATGTTGGTTATGCTTGTCTCAAATTCCGAACTTCAGGTGATCTGCCC T A TBCA Ensembl:ENSG00000171530 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1268276151 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15519969 14560 RMVar_ID_14560 Human_SNP_ID_237700964 A-to-I Human chr5 + 77784876 77784876 77784876 CTTCGCTGCTCCACTGCCAGTCCACACCTGCCACCAGCTCACCATGGATGATGATATCACCGCGC CTTCGCTGCTCCACTGCCAGTCCACACCTGCCGCCAGCTCACCATGGATGATGATATCACCGCGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879140974 Functional Loss SNV dbSNP153 33..33 33 - - - 14561 RMVar_ID_14561 Human_SNP_ID_237700972 A-to-I Human chr5 + 77784902 77784902 77784902 CCTGCCACCAGCTCACCATGGATGATGATATCACCGCGCTCGTCATTGACAACGGCTCCGGCATG CCTGCCACCAGCTCACCATGGATGATGATATCGCCGCGCTCGTCATTGACAACGGCTCCGGCATG A G ACTBP2 Ensembl:ENSG00000213763 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878862657 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1828368 14562 RMVar_ID_14562 Human_SNP_ID_237701051 A-to-I Human chr5 - 77785099 77785099 77785099 ATGTCGTCCCAGTTGGTGACAATGCCGTGCTCAATGGGGTACTTCAGGGTGAGGATGCCTCTCTT ATGTCGTCCCAGTTGGTGACAATGCCGTGCTCGATGGGGTACTTCAGGGTGAGGATGCCTCTCTT T C TBCA Ensembl:ENSG00000171530 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879222952 Functional Loss SNV dbSNP153 33..33 33 - - - 14563 RMVar_ID_14563 Human_SNP_ID_237701056 A-to-I Human chr5 - 77785111 77785111 77785111 CAGATCTTCTCCATGTCGTCCCAGTTGGTGACAATGCCGTGCTCAATGGGGTACTTCAGGGTGAG CAGATCTTCTCCATGTCGTCCCAGTTGGTGACGATGCCGTGCTCAATGGGGTACTTCAGGGTGAG T C TBCA Ensembl:ENSG00000171530 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs972908054 Functional Loss SNV dbSNP153 33..33 33 - - - 14564 RMVar_ID_14564 Human_SNP_ID_237785520 A-to-I Human chr5 - 78134626 78134626 78134626 TGAGGCAGGAGAATCACTTGAACCTGGTTGGCAGAGGTTGCAGTGAGCTGAGATCGCGCCATTGC TGAGGCAGGAGAATCACTTGAACCTGGTTGGCGGAGGTTGCAGTGAGCTGAGATCGCGCCATTGC T C AP3B1 Ensembl:ENSG00000132842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1030146395 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6209,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_232639,RMVar_hsa_circ_232637,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_102741,RMVar_hsa_circ_48055,RMVar_hsa_circ_65259,RMVar_hsa_circ_36563,RMVar_hsa_circ_7348,RMVar_hsa_circ_232648,RMVar_hsa_circ_232652,RMVar_hsa_circ_232654,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_232647,RMVar_hsa_circ_333887,RMVar_hsa_circ_232661,RMVar_hsa_circ_289887,RMVar_hsa_circ_360737,RMVar_hsa_circ_361542,RMVar_hsa_circ_232663,RMVar_hsa_circ_62264,RMVar_hsa_circ_358296,RMVar_hsa_circ_12581,RMVar_hsa_circ_266087,RMVar_hsa_circ_267300,RMVar_hsa_circ_366509,RMVar_hsa_circ_313811,RMVar_hsa_circ_58839,RMVar_hsa_circ_268776,RMVar_hsa_circ_232664,RMVar_hsa_circ_269720,RMVar_hsa_circ_266769 14565 RMVar_ID_14565 Human_SNP_ID_237785542 A-to-I Human chr5 - 78134716 78134716 78134716 CAACGTGGTTAAACCCCGTCTCTACTAAAAATACAAAAAAATTAGCCGGGTGTGGTGGCACATGC CAACGTGGTTAAACCCCGTCTCTACTAAAAATCCAAAAAAATTAGCCGGGTGTGGTGGCACATGC T G AP3B1 Ensembl:ENSG00000132842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978516754 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6209,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_232639,RMVar_hsa_circ_232637,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_102741,RMVar_hsa_circ_48055,RMVar_hsa_circ_65259,RMVar_hsa_circ_36563,RMVar_hsa_circ_7348,RMVar_hsa_circ_232648,RMVar_hsa_circ_232652,RMVar_hsa_circ_232654,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_232647,RMVar_hsa_circ_333887,RMVar_hsa_circ_232661,RMVar_hsa_circ_289887,RMVar_hsa_circ_360737,RMVar_hsa_circ_361542,RMVar_hsa_circ_232663,RMVar_hsa_circ_62264,RMVar_hsa_circ_358296,RMVar_hsa_circ_12581,RMVar_hsa_circ_266087,RMVar_hsa_circ_267300,RMVar_hsa_circ_366509,RMVar_hsa_circ_313811,RMVar_hsa_circ_58839,RMVar_hsa_circ_268776,RMVar_hsa_circ_232664,RMVar_hsa_circ_269720,RMVar_hsa_circ_266769 14566 RMVar_ID_14566 Human_SNP_ID_237793412 A-to-I Human chr5 - 78168499 78168499 78168499 AGTTGTCCAGCTGGATGCAGTGGTTCATGCCTATAATCCTAGGACTTTGGGAGGCTGAGGCAGGA AGTTGTCCAGCTGGATGCAGTGGTTCATGCCTGTAATCCTAGGACTTTGGGAGGCTGAGGCAGGA T C AP3B1 Ensembl:ENSG00000132842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1275210500 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6209,RMVar_hsa_circ_113230,RMVar_hsa_circ_115151,RMVar_hsa_circ_105659,RMVar_hsa_circ_232638,RMVar_hsa_circ_232639,RMVar_hsa_circ_232637,RMVar_hsa_circ_366536,RMVar_hsa_circ_370007,RMVar_hsa_circ_355667,RMVar_hsa_circ_295881,RMVar_hsa_circ_76410,RMVar_hsa_circ_112984,RMVar_hsa_circ_48055,RMVar_hsa_circ_65259,RMVar_hsa_circ_36563,RMVar_hsa_circ_232648,RMVar_hsa_circ_232650,RMVar_hsa_circ_232649,RMVar_hsa_circ_74195,RMVar_hsa_circ_100287,RMVar_hsa_circ_232647,RMVar_hsa_circ_232661,RMVar_hsa_circ_289887,RMVar_hsa_circ_12581,RMVar_hsa_circ_266087,RMVar_hsa_circ_267300,RMVar_hsa_circ_366509,RMVar_hsa_circ_268776,RMVar_hsa_circ_269720,RMVar_hsa_circ_266769,RMVar_hsa_circ_88465,RMVar_hsa_circ_326105,RMVar_hsa_circ_362040,RMVar_hsa_circ_318100,RMVar_hsa_circ_343272,RMVar_hsa_circ_317788,RMVar_hsa_circ_39363,RMVar_hsa_circ_124182,RMVar_hsa_circ_269167,RMVar_hsa_circ_232668,RMVar_hsa_circ_232669 14567 RMVar_ID_14567 Human_SNP_ID_237801611 A-to-I Human chr5 - 78202100 78202100 78202100 GGAAACTCCCCTTTTTAGAACCATCAGATCTTATAAGACTTATTCACGAACATAGCACGGGAAAG GGAAACTCCCCTTTTTAGAACCATCAGATCTTGTAAGACTTATTCACGAACATAGCACGGGAAAG T C AP3B1 Ensembl:ENSG00000132842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs776928487 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_295881,RMVar_hsa_circ_76410,RMVar_hsa_circ_112984,RMVar_hsa_circ_48055,RMVar_hsa_circ_65259,RMVar_hsa_circ_232648,RMVar_hsa_circ_232649,RMVar_hsa_circ_74195,RMVar_hsa_circ_232647,RMVar_hsa_circ_289887,RMVar_hsa_circ_266087,RMVar_hsa_circ_267300,RMVar_hsa_circ_269720,RMVar_hsa_circ_266769,RMVar_hsa_circ_88465,RMVar_hsa_circ_326105,RMVar_hsa_circ_318100,RMVar_hsa_circ_124182,RMVar_hsa_circ_269167,RMVar_hsa_circ_232668,RMVar_hsa_circ_232669,RMVar_hsa_circ_61283,RMVar_hsa_circ_232671,RMVar_hsa_circ_105490,RMVar_hsa_circ_50605 14568 RMVar_ID_14568 Human_SNP_ID_237839027 A-to-I Human chr5 - 78358966 78358966 78358966 CTAGATATCAAAAAGAGCAAGCAGTCTGTTGTACTCACCATCGCATCCTCAGCAGCTGCCCAGTG CTAGATATCAAAAAGAGCAAGCAGTCTGTTGTGCTCACCATCGCATCCTCAGCAGCTGCCCAGTG T C SCAMP1-AS1 Ensembl:ENSG00000245556 lincRNA intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs746634861 Functional Loss SNV dbSNP153 33..33 33 - - - 14569 RMVar_ID_14569 Human_SNP_ID_237943303 A-to-I Human chr5 - 78777681 78777681 78777681 GCCTGGCTATGTTTTGTATTTTTCGTAGAGATAGGGTTTCACCATGTTGGCCAGGCTGGTCTCAA GCCTGGCTATGTTTTGTATTTTTCGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTCAA T C ARSB Ensembl:ENSG00000113273 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569102350 Functional Loss SNV dbSNP153 33..33 33 - - - 14570 RMVar_ID_14570 Human_SNP_ID_237953556 A-to-I Human chr5 - 78821198 78821198 78821198 CCGGGAGGCAGAGGTTGCAGTGAGCTGAGATCACGCTATTGCACTCTAGCCTGGGTGACAAGAGC CCGGGAGGCAGAGGTTGCAGTGAGCTGAGATCGCGCTATTGCACTCTAGCCTGGGTGACAAGAGC T C ARSB Ensembl:ENSG00000113273 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417338388 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63906 14571 RMVar_ID_14571 Human_SNP_ID_237994035 A-to-I Human chr5 - 78985662 78985660 78985663 TTTTTTCTTATGAAAAATTGGCACTAATTATAATGTCTAACTGTCAGAGTTGTTGCAGGCTTTAC TTTTTTCTTATGAAAAATTGGCACTAATTAT___GTCTAACTGTCAGAGTTGTTGCAGGCTTTAC CATT C ARSB Ensembl:ENSG00000113273 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1038709961 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_103538,RMVar_hsa_circ_232691 14572 RMVar_ID_14572 Human_SNP_ID_237994036 A-to-I Human chr5 - 78985662 78985661 78985662 TTTTTTCTTATGAAAAATTGGCACTAATTATAATGTCTAACTGTCAGAGTTGTTGCAGGCTTTAC TTTTTTCTTATGAAAAATTGGCACTAATTATA_TGTCTAACTGTCAGAGTTGTTGCAGGCTTTAC AT A ARSB Ensembl:ENSG00000113273 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1394980910 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_103538,RMVar_hsa_circ_232691 14573 RMVar_ID_14573 Human_SNP_ID_237997304 A-to-I Human chr5 - 79000270 79000270 79000270 GGTGGGCATCTTCTTCATCTCATGGAGATTTTAAATGTGAGGAATATCATGGTGGTGGTATCACG GGTGGGCATCTTCTTCATCTCATGGAGATTTTGAATGTGAGGAATATCATGGTGGTGGTATCACG T C DMGDH,AC020937.1 Ensembl:ENSG00000132837,Ensembl:ENSG00000214890 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1448241143 Functional Loss SNV dbSNP153 33..33 33 - - - 14574 RMVar_ID_14574 Human_SNP_ID_237997310 A-to-I Human chr5 - 79000295 79000295 79000295 TGAGGATGATGGGGAAAGAGCAGCTGGTGGGCATCTTCTTCATCTCATGGAGATTTTAAATGTGA TGAGGATGATGGGGAAAGAGCAGCTGGTGGGCGTCTTCTTCATCTCATGGAGATTTTAAATGTGA T C DMGDH,AC020937.1 Ensembl:ENSG00000132837,Ensembl:ENSG00000214890 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1400936150 Functional Loss SNV dbSNP153 33..33 33 - - - 14575 RMVar_ID_14575 Human_SNP_ID_238054387 A-to-I Human chr5 - 79226497 79226497 79226497 CCGCCCGCCTCGCCTCCCAAAGCGCTAGGATTACAGGGGTGAGCCACCACACCCGGCCAAGAAAC CCGCCCGCCTCGCCTCCCAAAGCGCTAGGATTGCAGGGGTGAGCCACCACACCCGGCCAAGAAAC T C DMGDH Ensembl:ENSG00000132837 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs575773196 Functional Loss SNV dbSNP153 33..33 33 - - - 14576 RMVar_ID_14576 Human_SNP_ID_238054390 A-to-I Human chr5 - 79226503 79226503 79226503 GACAATCCGCCCGCCTCGCCTCCCAAAGCGCTAGGATTACAGGGGTGAGCCACCACACCCGGCCA GACAATCCGCCCGCCTCGCCTCCCAAAGCGCTGGGATTACAGGGGTGAGCCACCACACCCGGCCA T C DMGDH Ensembl:ENSG00000132837 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1203334709 Functional Loss SNV dbSNP153 33..33 33 - - - 14577 RMVar_ID_14577 Human_SNP_ID_238055997 A-to-I Human chr5 - 79232918 79232918 79232918 GGCTGTAATCGGGAGGCTGAGGCAGGAGAATCACTTGAACCTGGGAGGCAGAAGTGGCAGTGAAC GGCTGTAATCGGGAGGCTGAGGCAGGAGAATCCCTTGAACCTGGGAGGCAGAAGTGGCAGTGAAC T G DMGDH Ensembl:ENSG00000132837 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277886432 Functional Loss SNV dbSNP153 33..33 33 - - - 14578 RMVar_ID_14578 Human_SNP_ID_238056014 A-to-I Human chr5 - 79232978 79232978 79232978 CCCATCTCTGCTAAAAATACAAAAATTAGCCAAGCGTGGTGGTGGGCACCTGTAATCCCAGGCTG CCCATCTCTGCTAAAAATACAAAAATTAGCCAGGCGTGGTGGTGGGCACCTGTAATCCCAGGCTG T C DMGDH Ensembl:ENSG00000132837 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs914192729 Functional Loss SNV dbSNP153 33..33 33 - - - 14579 RMVar_ID_14579 Human_SNP_ID_238067932 A-to-I Human chr5 + 79274606 79274606 79274606 ATTTTTGTATTTTCAGTAGAAACTGTTTCACCATGTTGCCAAGGCTGGTCTCGAACTCCTGACCT ATTTTTGTATTTTCAGTAGAAACTGTTTCACCGTGTTGCCAAGGCTGGTCTCGAACTCCTGACCT A G JMY Ensembl:ENSG00000152409 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1330740544 Functional Loss SNV dbSNP153 33..33 33 - - - 14580 RMVar_ID_14580 Human_SNP_ID_238069960 A-to-I Human chr5 + 79282086 79282084 79282086 AAAATTGGCCGGGCATGGTGGTGGCCACCTGTAGTCCCAGCTACTTGGGAGGCTGAGGTGGGAGA AAAATTGGCCGGGCATGGTGGTGGCCACCTG__GTCCCAGCTACTTGGGAGGCTGAGGTGGGAGA GTA G JMY Ensembl:ENSG00000152409 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1408405448 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_28044,RMVar_hsa_circ_366022,RMVar_hsa_circ_368282,RMVar_hsa_circ_331918,RMVar_hsa_circ_267524,RMVar_hsa_circ_232703 14581 RMVar_ID_14581 Human_SNP_ID_238077265 A-to-I Human chr5 + 79313321 79313321 79313321 CATGCCTGTGGTTCCGGCCATTTGGGTGGCTGAAGTGGGAGGATTACCTGAGCCAGGGAGGTCAT CATGCCTGTGGTTCCGGCCATTTGGGTGGCTGCAGTGGGAGGATTACCTGAGCCAGGGAGGTCAT A C JMY Ensembl:ENSG00000152409 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1376384428 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15522968 RMVar_hsa_circ_267524,RMVar_hsa_circ_323025,RMVar_hsa_circ_232709,RMVar_hsa_circ_232707,RMVar_hsa_circ_101696,RMVar_hsa_circ_91530,RMVar_hsa_circ_232710,RMVar_hsa_circ_355177,RMVar_hsa_circ_232711 14582 RMVar_ID_14582 Human_SNP_ID_238123233 A-to-I Human chr5 - 79498974 79498974 79498974 AAAATTAGCTGGGCATGGTGGTATGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTAGCTGGGCATGGTGGTATGCGCCTGTGGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA T C HOMER1 Ensembl:ENSG00000152413 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1361125579 Functional Loss SNV dbSNP153 33..33 33 - - - 14583 RMVar_ID_14583 Human_SNP_ID_238129004 A-to-I Human chr5 + 79520067 79520067 79520067 CTCACTGCAACCTCCGCCTCCCGGGTTCAAGCAGTTCTCTGCCTCGGCCTCCTGAGTAGCTGGGA CTCACTGCAACCTCCGCCTCCCGGGTTCAAGCGGTTCTCTGCCTCGGCCTCCTGAGTAGCTGGGA A G RF00017-4509 RNACentral:URS0000970E28 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1013783618 Functional Loss SNV dbSNP153 33..33 33 - - - 14584 RMVar_ID_14584 Human_SNP_ID_238155911 A-to-I Human chr5 + 79625873 79625873 79625873 TTTTTTTGATATAGAGTCTAGCTCTGCCGCCCAGGCTGGAGTGCAGTGGTGCGATCTCGGCTCAC TTTTTTTGATATAGAGTCTAGCTCTGCCGCCCTGGCTGGAGTGCAGTGGTGCGATCTCGGCTCAC A T TENT2 Ensembl:ENSG00000164329 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1396272471 Functional Loss SNV dbSNP153 33..33 33 - - - 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 14585 RMVar_ID_14585 Human_SNP_ID_238157934 A-to-I Human chr5 + 79633596 79633596 79633596 GCGCCACCATGCCCGGCTAATTTTGTGTTTTTAGTAGAGACGGGGTTTCTCCATGTTGGTCAGGC GCGCCACCATGCCCGGCTAATTTTGTGTTTTTGGTAGAGACGGGGTTTCTCCATGTTGGTCAGGC A G TENT2 Ensembl:ENSG00000164329 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1034627098 Functional Loss SNV dbSNP153 33..33 33 - - - 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 14586 RMVar_ID_14586 Human_SNP_ID_238158112 A-to-I Human chr5 + 79634046 79634046 79634046 AAAAAATTAGCTGGACCTGGTGGCGGACGCCTATAGTCCCAGCTACTCGGGAGAATGGCATGAAC AAAAAATTAGCTGGACCTGGTGGCGGACGCCTGTAGTCCCAGCTACTCGGGAGAATGGCATGAAC A G TENT2 Ensembl:ENSG00000164329 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1001932567 Functional Loss SNV dbSNP153 33..33 33 - - - 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 14587 RMVar_ID_14587 Human_SNP_ID_238158906 A-to-I Human chr5 + 79637123 79637123 79637123 AGATGTGGTGCTGCACACCTTTAGTCCCAGCTACTTGCAGGGCTGAGATGGGAGGATTGCTTGAC AGATGTGGTGCTGCACACCTTTAGTCCCAGCTGCTTGCAGGGCTGAGATGGGAGGATTGCTTGAC A G TENT2 Ensembl:ENSG00000164329 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs570276810 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15525444 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 14588 RMVar_ID_14588 Human_SNP_ID_238159662 A-to-I Human chr5 + 79640181 79640181 79640181 GGGACGCTGAGGCAGGAGAACCGCTTGAACCCAGGAGGCTGAGGTTGCAGTGAGCCGAGATCGCA GGGACGCTGAGGCAGGAGAACCGCTTGAACCCGGGAGGCTGAGGTTGCAGTGAGCCGAGATCGCA A G TENT2 Ensembl:ENSG00000164329 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs974666613 Functional Loss SNV dbSNP153 33..33 33 - - - 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 14589 RMVar_ID_14589 Human_SNP_ID_238161296 A-to-I Human chr5 + 79646848 79646848 79646848 TGGAGTGCAGTGGCATGATCATAGCTCACTGTAACCTCAAATGCCTGGACTCAAGTGATCCTCCC TGGAGTGCAGTGGCATGATCATAGCTCACTGTCACCTCAAATGCCTGGACTCAAGTGATCCTCCC A C TENT2 Ensembl:ENSG00000164329 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985769070 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15525911 RMVar_hsa_circ_16464,RMVar_hsa_circ_116764,RMVar_hsa_circ_232728,RMVar_hsa_circ_63265,RMVar_hsa_circ_281438,RMVar_hsa_circ_361680,RMVar_hsa_circ_60940,RMVar_hsa_circ_232732,RMVar_hsa_circ_37775,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_110147,RMVar_hsa_circ_232738,RMVar_hsa_circ_232739,RMVar_hsa_circ_232737,RMVar_hsa_circ_71421,RMVar_hsa_circ_353107,RMVar_hsa_circ_334278,RMVar_hsa_circ_352930,RMVar_hsa_circ_375927,RMVar_hsa_circ_362318,RMVar_hsa_circ_94775,RMVar_hsa_circ_232750,RMVar_hsa_circ_232751,RMVar_hsa_circ_232752,RMVar_hsa_circ_232748,RMVar_hsa_circ_232749,RMVar_hsa_circ_232756,RMVar_hsa_circ_277897,RMVar_hsa_circ_314249,RMVar_hsa_circ_360206,RMVar_hsa_circ_305289,RMVar_hsa_circ_273142,RMVar_hsa_circ_37542,RMVar_hsa_circ_232754,RMVar_hsa_circ_232755,RMVar_hsa_circ_232753,RMVar_hsa_circ_232761,RMVar_hsa_circ_3844,RMVar_hsa_circ_41143,RMVar_hsa_circ_71302,RMVar_hsa_circ_110910,RMVar_hsa_circ_371307,RMVar_hsa_circ_232758,RMVar_hsa_circ_323651,RMVar_hsa_circ_274827,RMVar_hsa_circ_286036,RMVar_hsa_circ_294556,RMVar_hsa_circ_232759,RMVar_hsa_circ_338724,RMVar_hsa_circ_287880,RMVar_hsa_circ_285675,RMVar_hsa_circ_232763,RMVar_hsa_circ_232764,RMVar_hsa_circ_232762,RMVar_hsa_circ_232760 14590 RMVar_ID_14590 Human_SNP_ID_238170611 A-to-I Human chr5 + 79684307 79684307 79684307 TCCTTCATAAATACTATATATTTTTTTGAGACAGGGTCTTGCTCTGTTACCCAGACTCAGGCAGC TCCTTCATAAATACTATATATTTTTTTGAGACGGGGTCTTGCTCTGTTACCCAGACTCAGGCAGC A G TENT2 Ensembl:ENSG00000164329 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1448564000 Functional Loss SNV dbSNP153 33..33 33 - - - 14591 RMVar_ID_14591 Human_SNP_ID_238279456 A-to-I Human chr5 - 80142384 80142384 80142384 TATTAAAAATAGAAAAATTAGCCGGGCATGGTAGCGTGTGCCTGTAATGCCAGCTACTCGAAGGC TATTAAAAATAGAAAAATTAGCCGGGCATGGTGGCGTGTGCCTGTAATGCCAGCTACTCGAAGGC T C SERINC5 Ensembl:ENSG00000164300 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs953049293 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269699,RMVar_hsa_circ_232780 14592 RMVar_ID_14592 Human_SNP_ID_238321910 A-to-I Human chr5 + 80299792 80299792 80299792 AGCGAGGCCAGGATGGAGCCTCTGATCCACACAGAGTACTTGCACTCAGGAGGAGCAATGATCTT AGCGAGGCCAGGATGGAGCCTCTGATCCACACGGAGTACTTGCACTCAGGAGGAGCAATGATCTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1561470929 Functional Loss SNV dbSNP153 33..33 33 - - - 14593 RMVar_ID_14593 Human_SNP_ID_238321913 A-to-I Human chr5 + 80299803 80299803 80299803 GATGGAGCCTCTGATCCACACAGAGTACTTGCACTCAGGAGGAGCAATGATCTTGATCTTCATTG GATGGAGCCTCTGATCCACACAGAGTACTTGCGCTCAGGAGGAGCAATGATCTTGATCTTCATTG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs757692625 Functional Loss SNV dbSNP153 33..33 33 - - - 14594 RMVar_ID_14594 Human_SNP_ID_238362692 A-to-I Human chr5 + 80455475 80455475 80455475 AGAATTACTTGAACCCAGGAAGTGGAGGTTGCAATGAGTCGAGATTGCACCGCTGCACTCCAGCC AGAATTACTTGAACCCAGGAAGTGGAGGTTGCCATGAGTCGAGATTGCACCGCTGCACTCCAGCC A C ZFYVE16 Ensembl:ENSG00000039319 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs111753038 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_1137 RMVar_hsa_circ_58651,RMVar_hsa_circ_22911,RMVar_hsa_circ_339304,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_11184,RMVar_hsa_circ_367969,RMVar_hsa_circ_267214,RMVar_hsa_circ_274900,RMVar_hsa_circ_232803,RMVar_hsa_circ_343287,RMVar_hsa_circ_366272,RMVar_hsa_circ_267480,RMVar_hsa_circ_352948,RMVar_hsa_circ_232804 14595 RMVar_ID_14595 Human_SNP_ID_238362693 A-to-I Human chr5 + 80455475 80455475 80455475 AGAATTACTTGAACCCAGGAAGTGGAGGTTGCAATGAGTCGAGATTGCACCGCTGCACTCCAGCC AGAATTACTTGAACCCAGGAAGTGGAGGTTGCGATGAGTCGAGATTGCACCGCTGCACTCCAGCC A G ZFYVE16 Ensembl:ENSG00000039319 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs111753038 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_1137 RMVar_hsa_circ_58651,RMVar_hsa_circ_22911,RMVar_hsa_circ_339304,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_11184,RMVar_hsa_circ_367969,RMVar_hsa_circ_267214,RMVar_hsa_circ_274900,RMVar_hsa_circ_232803,RMVar_hsa_circ_343287,RMVar_hsa_circ_366272,RMVar_hsa_circ_267480,RMVar_hsa_circ_352948,RMVar_hsa_circ_232804 14596 RMVar_ID_14596 Human_SNP_ID_238365698 A-to-I Human chr5 + 80467806 80467806 80467806 ACTGTCCCTAAGGAAACAAAGACATTACACTTACAAGACAAAGGGTATAAATCAATTATTTAAAA ACTGTCCCTAAGGAAACAAAGACATTACACTTCCAAGACAAAGGGTATAAATCAATTATTTAAAA A C ZFYVE16 Ensembl:ENSG00000039319 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs914536225 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22911,RMVar_hsa_circ_359630,RMVar_hsa_circ_339601,RMVar_hsa_circ_268011,RMVar_hsa_circ_232798,RMVar_hsa_circ_60124,RMVar_hsa_circ_367969,RMVar_hsa_circ_274900,RMVar_hsa_circ_232803,RMVar_hsa_circ_343287,RMVar_hsa_circ_366272,RMVar_hsa_circ_232805,RMVar_hsa_circ_232804,RMVar_hsa_circ_332341,RMVar_hsa_circ_60109,RMVar_hsa_circ_298248,RMVar_hsa_circ_232807,RMVar_hsa_circ_303787 14597 RMVar_ID_14597 Human_SNP_ID_238369015 A-to-I Human chr5 - 80481958 80481958 80481958 AAAATTATCTAGGCGTGGTGGTACACACCTGTAGTCACAGCTACTCAGGAGGCTGAGACAGGAGA AAAATTATCTAGGCGTGGTGGTACACACCTGTTGTCACAGCTACTCAGGAGGCTGAGACAGGAGA T A AC008771.1 Ensembl:ENSG00000249042 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1284111534 Functional Loss SNV dbSNP153 33..33 33 - - - 14598 RMVar_ID_14598 Human_SNP_ID_238369251 A-to-I Human chr5 - 80483041 80483040 80483042 AACATGGTGAAACTCGTCTCTACTACAAACATAAAAAAATTAGCTGGGCGTGGTACCACGCACCT AACATGGTGAAACTCGTCTCTACTACAAACA__AAAAAATTAGCTGGGCGTGGTACCACGCACCT TTA T AC008771.1 Ensembl:ENSG00000249042 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1360613070 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_27517555 14599 RMVar_ID_14599 Human_SNP_ID_238372825 A-to-I Human chr5 + 80497385 80497385 80497385 TGCAGTGAGCTGAGATCATGCCCCTGCACTCCAGCCTGAGTGACAGAGCAAGACTCCGGCTCAAA TGCAGTGAGCTGAGATCATGCCCCTGCACTCCGGCCTGAGTGACAGAGCAAGACTCCGGCTCAAA A G FAM151B Ensembl:ENSG00000152380 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1448356841 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94165,RMVar_hsa_circ_232808,RMVar_hsa_circ_123551,RMVar_hsa_circ_358502,RMVar_hsa_circ_232810,RMVar_hsa_circ_41732,RMVar_hsa_circ_232809 14600 RMVar_ID_14600 Human_SNP_ID_238401093 A-to-I Human chr5 - 80609929 80609929 80609929 TAGAGGCAGGGTCTTATTATGTTGACCAGGCTAGTCTGAAACTCCTGGCCTCAAGCAGTCCTCCC TAGAGGCAGGGTCTTATTATGTTGACCAGGCTTGTCTGAAACTCCTGGCCTCAAGCAGTCCTCCC T A LINC01337 Ensembl:ENSG00000251221 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909568732 Functional Loss SNV dbSNP153 33..33 33 - - - 14601 RMVar_ID_14601 Human_SNP_ID_238401094 A-to-I Human chr5 - 80609929 80609929 80609929 TAGAGGCAGGGTCTTATTATGTTGACCAGGCTAGTCTGAAACTCCTGGCCTCAAGCAGTCCTCCC TAGAGGCAGGGTCTTATTATGTTGACCAGGCTGGTCTGAAACTCCTGGCCTCAAGCAGTCCTCCC T C LINC01337 Ensembl:ENSG00000251221 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909568732 Functional Loss SNV dbSNP153 33..33 33 - - - 14602 RMVar_ID_14602 Human_SNP_ID_238404906 A-to-I Human chr5 - 80624636 80624636 80624636 CCCACTGCAACCTCTGCCTCCCGGGTTCAAGCAGTTCACCCTCAGCCTCCCCAATAGTTGGGATT CCCACTGCAACCTCTGCCTCCCGGGTTCAAGCCGTTCACCCTCAGCCTCCCCAATAGTTGGGATT T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs753073337 Functional Loss SNV dbSNP153 33..33 33 - - - 14603 RMVar_ID_14603 Human_SNP_ID_238405620 A-to-I Human chr5 - 80627470 80627470 80627470 ATTGTGGCGCACACCTGTATTCCCATCTAGTCAGGAAGCTGAGATGGAAGAATTAATTGAGCCCA ATTGTGGCGCACACCTGTATTCCCATCTAGTCTGGAAGCTGAGATGGAAGAATTAATTGAGCCCA T A DHFR Ensembl:ENSG00000228716 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1170399482 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_647476,Human_RBP_ID_7476631,Human_RBP_ID_9181047,Human_RBP_ID_15529568,Human_RBP_ID_18054047,Human_RBP_ID_18361855,Human_RBP_ID_23194193,Human_RBP_ID_26528525 14604 RMVar_ID_14604 Human_SNP_ID_238405621 A-to-I Human chr5 - 80627470 80627470 80627470 ATTGTGGCGCACACCTGTATTCCCATCTAGTCAGGAAGCTGAGATGGAAGAATTAATTGAGCCCA ATTGTGGCGCACACCTGTATTCCCATCTAGTCGGGAAGCTGAGATGGAAGAATTAATTGAGCCCA T C DHFR Ensembl:ENSG00000228716 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1170399482 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_647476,Human_RBP_ID_7476631,Human_RBP_ID_9181047,Human_RBP_ID_15529568,Human_RBP_ID_18054047,Human_RBP_ID_18361855,Human_RBP_ID_23194193,Human_RBP_ID_26528525 14605 RMVar_ID_14605 Human_SNP_ID_238405627 A-to-I Human chr5 - 80627510 80627510 80627510 AAAGCCCCATCTCTACAAAAAACACAAAAATTAGCTGGGCATTGTGGCGCACACCTGTATTCCCA AAAGCCCCATCTCTACAAAAAACACAAAAATTGGCTGGGCATTGTGGCGCACACCTGTATTCCCA T C DHFR Ensembl:ENSG00000228716 Protein coding 3'UTR GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,29796672,31158229 RNA-Seq:(High) rs1261924721 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26528526 14606 RMVar_ID_14606 Human_SNP_ID_238405628 A-to-I Human chr5 - 80627513 80627513 80627513 GGCAAAGCCCCATCTCTACAAAAAACACAAAAATTAGCTGGGCATTGTGGCGCACACCTGTATTC GGCAAAGCCCCATCTCTACAAAAAACACAAAACTTAGCTGGGCATTGTGGCGCACACCTGTATTC T G DHFR Ensembl:ENSG00000228716 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1275067281 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26528526 14607 RMVar_ID_14607 Human_SNP_ID_238405629 A-to-I Human chr5 - 80627514 80627514 80627514 TGGCAAAGCCCCATCTCTACAAAAAACACAAAAATTAGCTGGGCATTGTGGCGCACACCTGTATT TGGCAAAGCCCCATCTCTACAAAAAACACAAAGATTAGCTGGGCATTGTGGCGCACACCTGTATT T C DHFR Ensembl:ENSG00000228716 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1461494593 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26528526 14608 RMVar_ID_14608 Human_SNP_ID_238405635 A-to-I Human chr5 - 80627541 80627541 80627541 GATCACTTGAGACCAGCTTGGGCAACATGGCAAAGCCCCATCTCTACAAAAAACACAAAAATTAG GATCACTTGAGACCAGCTTGGGCAACATGGCAGAGCCCCATCTCTACAAAAAACACAAAAATTAG T C DHFR Ensembl:ENSG00000228716 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1231588485 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18054049,Human_RBP_ID_26528526 14609 RMVar_ID_14609 Human_SNP_ID_238405636 A-to-I Human chr5 - 80627542 80627542 80627542 AGATCACTTGAGACCAGCTTGGGCAACATGGCAAAGCCCCATCTCTACAAAAAACACAAAAATTA AGATCACTTGAGACCAGCTTGGGCAACATGGCGAAGCCCCATCTCTACAAAAAACACAAAAATTA T C DHFR Ensembl:ENSG00000228716 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1469947204 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18054049,Human_RBP_ID_26529133 14610 RMVar_ID_14610 Human_SNP_ID_238405637 A-to-I Human chr5 - 80627547 80627547 80627547 CAGGCAGATCACTTGAGACCAGCTTGGGCAACATGGCAAAGCCCCATCTCTACAAAAAACACAAA CAGGCAGATCACTTGAGACCAGCTTGGGCAACGTGGCAAAGCCCCATCTCTACAAAAAACACAAA T C DHFR Ensembl:ENSG00000228716 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1178328061 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4841507,Human_RBP_ID_18054049,Human_RBP_ID_26529133 14611 RMVar_ID_14611 Human_SNP_ID_238405641 A-to-I Human chr5 - 80627559 80627559 80627559 GGGAGGCTAAGGCAGGCAGATCACTTGAGACCAGCTTGGGCAACATGGCAAAGCCCCATCTCTAC GGGAGGCTAAGGCAGGCAGATCACTTGAGACCGGCTTGGGCAACATGGCAAAGCCCCATCTCTAC T C DHFR Ensembl:ENSG00000228716 Protein coding 3'UTR GSE38233;GSE100210;GSE112787;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;293 Flip-In T-REx cells,empty vector;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,29967493,31158229 RNA-Seq:(High) rs1410826356 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18054049,Human_RBP_ID_21199399,Human_RBP_ID_26529133 14612 RMVar_ID_14612 Human_SNP_ID_238405654 A-to-I Human chr5 - 80627604 80627604 80627604 AAACCAGCCAGGCACAGTGGCTCACACCTGTAATCCCAGCGCTTTGGGAGGCTAAGGCAGGCAGA AAACCAGCCAGGCACAGTGGCTCACACCTGTATTCCCAGCGCTTTGGGAGGCTAAGGCAGGCAGA T A DHFR Ensembl:ENSG00000228716 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs764279681 Functional Loss SNV dbSNP153 33..33 33 - - - 14613 RMVar_ID_14613 Human_SNP_ID_238405655 A-to-I Human chr5 - 80627604 80627604 80627604 AAACCAGCCAGGCACAGTGGCTCACACCTGTAATCCCAGCGCTTTGGGAGGCTAAGGCAGGCAGA AAACCAGCCAGGCACAGTGGCTCACACCTGTAGTCCCAGCGCTTTGGGAGGCTAAGGCAGGCAGA T C DHFR Ensembl:ENSG00000228716 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs764279681 Functional Loss SNV dbSNP153 33..33 33 - - - 14614 RMVar_ID_14614 Human_SNP_ID_238405656 A-to-I Human chr5 - 80627605 80627605 80627605 AAAACCAGCCAGGCACAGTGGCTCACACCTGTAATCCCAGCGCTTTGGGAGGCTAAGGCAGGCAG AAAACCAGCCAGGCACAGTGGCTCACACCTGTGATCCCAGCGCTTTGGGAGGCTAAGGCAGGCAG T C DHFR Ensembl:ENSG00000228716 Protein coding 3'UTR GSE47997;GSE100210;GSE99789 K562 cells&HepG2 cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 23474544,29129909,29796672 RNA-Seq:(High) rs1327096688 Functional Loss SNV dbSNP153 33..33 33 - - - 14615 RMVar_ID_14615 Human_SNP_ID_238405659 A-to-I Human chr5 - 80627611 80627611 80627611 AAAAGAAAAACCAGCCAGGCACAGTGGCTCACACCTGTAATCCCAGCGCTTTGGGAGGCTAAGGC AAAAGAAAAACCAGCCAGGCACAGTGGCTCACGCCTGTAATCCCAGCGCTTTGGGAGGCTAAGGC T C DHFR Ensembl:ENSG00000228716 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs11550953 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26529134 14616 RMVar_ID_14616 Human_SNP_ID_238405665 A-to-I Human chr5 - 80627627 80627627 80627627 GAAGTAGAGAGAAAATAAAAGAAAAACCAGCCAGGCACAGTGGCTCACACCTGTAATCCCAGCGC GAAGTAGAGAGAAAATAAAAGAAAAACCAGCCGGGCACAGTGGCTCACACCTGTAATCCCAGCGC T C DHFR Ensembl:ENSG00000228716 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1282106824 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23048258,Human_RBP_ID_26529134 14617 RMVar_ID_14617 Human_SNP_ID_238405728 A-to-I Human chr5 - 80627969 80627969 80627969 GAACTCGTGACCGCAAGCGATTCACCCACCTCAGCCTCCCAAAGTGCTGGGATTACCGGCTTGAG GAACTCGTGACCGCAAGCGATTCACCCACCTCGGCCTCCCAAAGTGCTGGGATTACCGGCTTGAG T C DHFR Ensembl:ENSG00000228716 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1278913894 Functional Loss SNV dbSNP153 33..33 33 - - - 14618 RMVar_ID_14618 Human_SNP_ID_238405740 A-to-I Human chr5 - 80628007 80628007 80628007 TAGAGATGGGGTTTCACCATGTTGGTCAGGCTAGTCTCGAACTCGTGACCGCAAGCGATTCACCC TAGAGATGGGGTTTCACCATGTTGGTCAGGCTGGTCTCGAACTCGTGACCGCAAGCGATTCACCC T C DHFR Ensembl:ENSG00000228716 Protein coding 3'UTR GSE38233;GSE100210;GSE112787 cultured B-cells;HepG2 cell line;293 Flip-In T-REx cells,empty vector - 24183664,29129909,29967493 RNA-Seq:(High) rs1129243 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_647481 14619 RMVar_ID_14619 Human_SNP_ID_238405745 A-to-I Human chr5 - 80628024 80628024 80628024 GTATTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGTCAGGCTAGTCTCGAACTCGTGA GTATTTTGTATTTTTAGTAGAGATGGGGTTTCGCCATGTTGGTCAGGCTAGTCTCGAACTCGTGA T C DHFR Ensembl:ENSG00000228716 Protein coding 3'UTR GSE38233;GSE112787;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;293 Flip-In T-REx cells,empty vector;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29967493,31158229,32596459 RNA-Seq:(High) rs879172237 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_647481,Human_RBP_ID_23194200 14620 RMVar_ID_14620 Human_SNP_ID_238405748 A-to-I Human chr5 - 80628038 80628038 80628038 CCCGGCTAATTTTTGTATTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGTCAGGCTAG CCCGGCTAATTTTTGTATTTTGTATTTTTAGTGGAGATGGGGTTTCACCATGTTGGTCAGGCTAG T C DHFR Ensembl:ENSG00000228716 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1282995756 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_647481,Human_RBP_ID_4841516 14621 RMVar_ID_14621 Human_SNP_ID_238405766 A-to-I Human chr5 - 80628087 80628087 80628087 CTCCTGCCTCAGGCTCCCAAGTAGCTAGGACCAGGTGCGCGCCACCACGCCCGGCTAATTTTTGT CTCCTGCCTCAGGCTCCCAAGTAGCTAGGACCGGGTGCGCGCCACCACGCCCGGCTAATTTTTGT T C DHFR Ensembl:ENSG00000228716 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474262414 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7476644,Human_RBP_ID_18054054 14622 RMVar_ID_14622 Human_SNP_ID_238405768 A-to-I Human chr5 - 80628093 80628093 80628093 GCGATTCTCCTGCCTCAGGCTCCCAAGTAGCTAGGACCAGGTGCGCGCCACCACGCCCGGCTAAT GCGATTCTCCTGCCTCAGGCTCCCAAGTAGCTGGGACCAGGTGCGCGCCACCACGCCCGGCTAAT T C DHFR Ensembl:ENSG00000228716 Protein coding 3'UTR GSE100210;GSE112787;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;293 Flip-In T-REx cells,empty vector;Bronchiolar epithelium,BERP35T1 cell line - 29129909,29967493,31158229 RNA-Seq:(High) rs1215903653 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4857342,Human_RBP_ID_7476644 14623 RMVar_ID_14623 Human_SNP_ID_238405782 A-to-I Human chr5 - 80628171 80628171 80628171 CGTTTCGCTCTTGTTGCCCAGGCTAGCATGCAATGGTGTGACCTCGGCTTACTGCAACCTCCGCC CGTTTCGCTCTTGTTGCCCAGGCTAGCATGCAGTGGTGTGACCTCGGCTTACTGCAACCTCCGCC T C DHFR Ensembl:ENSG00000228716 Protein coding 3'UTR GSE100210;GSE112787;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;293 Flip-In T-REx cells,empty vector;ASD brains,Fragile X samples from NIH NeuroBioBank;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,29967493,30559470,31158229,31158229 RNA-Seq:(High) rs1311573544 Functional Loss SNV dbSNP153 33..33 33 - - - 14624 RMVar_ID_14624 Human_SNP_ID_238405785 A-to-I Human chr5 - 80628179 80628179 80628179 TTAGACAGCGTTTCGCTCTTGTTGCCCAGGCTAGCATGCAATGGTGTGACCTCGGCTTACTGCAA TTAGACAGCGTTTCGCTCTTGTTGCCCAGGCTGGCATGCAATGGTGTGACCTCGGCTTACTGCAA T C DHFR Ensembl:ENSG00000228716 Protein coding 3'UTR GSE112787;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 293 Flip-In T-REx cells,empty vector;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 29967493,31158229,31158229 RNA-Seq:(High) rs1178767396 Functional Loss SNV dbSNP153 33..33 33 - - - 14625 RMVar_ID_14625 Human_SNP_ID_238411508 A-to-I Human chr5 - 80650999 80650999 80650999 AACCCATTCCACCTTACTACCAAACAACCTTAACCAAACCATTTACTCAAATAAAGTATAGGCGA AACCCATTCCACCTTACTACCAAACAACCTTAGCCAAACCATTTACTCAAATAAAGTATAGGCGA T C DHFR Ensembl:ENSG00000228716 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs80057978 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8236676,Human_RBP_ID_21944716 RMVar_hsa_circ_54991,RMVar_hsa_circ_367945 14626 RMVar_ID_14626 Human_SNP_ID_238431528 A-to-I Human chr5 + 80725543 80725543 80725543 CATGCTTTCCAGGCAGTTACAGAGTTTTATGCAAAAGATACAGTTGACATCAAAGGTAAATATTT CATGCTTTCCAGGCAGTTACAGAGTTTTATGCCAAAGATACAGTTGACATCAAAGGTAAATATTT A C MSH3 Ensembl:ENSG00000113318 Protein coding CDS GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs745850629 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18847999 Human_Splice_Rec_667702,Human_Splice_Rec_667703,Human_Splice_Rec_667748,Human_Splice_Rec_667749,Human_Splice_Rec_667792,Human_Splice_Rec_667793,Human_Splice_Rec_667834,Human_Splice_Rec_667835,Human_Splice_Rec_667866,Human_Splice_Rec_667867 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_26139,RMVar_hsa_circ_292533,RMVar_hsa_circ_232824,RMVar_hsa_circ_232826,RMVar_hsa_circ_232827,RMVar_hsa_circ_232825,RMVar_hsa_circ_327683,RMVar_hsa_circ_359507,RMVar_hsa_circ_232828,RMVar_hsa_circ_342652,RMVar_hsa_circ_306440,RMVar_hsa_circ_279935,RMVar_hsa_circ_286919,RMVar_hsa_circ_29987,RMVar_hsa_circ_232829,RMVar_hsa_circ_232831,RMVar_hsa_circ_232833,RMVar_hsa_circ_232834,RMVar_hsa_circ_232832,RMVar_hsa_circ_232830 14627 RMVar_ID_14627 Human_SNP_ID_238442612 A-to-I Human chr5 - 80771472 80771472 80771472 TAGCATTAGTCCTTTTTTTTTTTTTTTGAGACAGGGTTTCTCTCTGTTGCCCAGGCTGGAGTACA TAGCATTAGTCCTTTTTTTTTTTTTTTGAGACTGGGTTTCTCTCTGTTGCCCAGGCTGGAGTACA T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1561472728 Functional Loss SNV dbSNP153 33..33 33 - - - 14628 RMVar_ID_14628 Human_SNP_ID_238502404 A-to-I Human chr5 + 81018050 81018050 81018050 AGAATCACTTGAACCTGGGAGGCAGCAGTTGCAGTGAGCCAAGATCGCGCCACTGCACTCCAGCC AGAATCACTTGAACCTGGGAGGCAGCAGTTGCCGTGAGCCAAGATCGCGCCACTGCACTCCAGCC A C RASGRF2 Ensembl:ENSG00000113319 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs555578794 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112528,RMVar_hsa_circ_104221,RMVar_hsa_circ_232859,RMVar_hsa_circ_118878,RMVar_hsa_circ_232860,RMVar_hsa_circ_232863 14629 RMVar_ID_14629 Human_SNP_ID_238565650 A-to-I Human chr5 - 81288522 81288522 81288522 AAATTAGCCAGGCGTGGTGGCAGGCCCTTGTAATCCCAGCTACTCGGGAGGCTGAGGCAAGAGAA AAATTAGCCAGGCGTGGTGGCAGGCCCTTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAAGAGAA T C CKMT2-AS1 Ensembl:ENSG00000247572 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1165063000 Functional Loss SNV dbSNP153 33..33 33 - - - 14630 RMVar_ID_14630 Human_SNP_ID_238596279 A-to-I Human chr5 - 81415790 81415790 81415790 CTCCTGCCTCAGCCTCCCGAGTGGCTGGGACTACAGGTGCTCACCACCATGCCCAGCTAATTTTT CTCCTGCCTCAGCCTCCCGAGTGGCTGGGACTGCAGGTGCTCACCACCATGCCCAGCTAATTTTT T C SSBP2 Ensembl:ENSG00000145687 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1235282728 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1400348 14631 RMVar_ID_14631 Human_SNP_ID_238669386 A-to-I Human chr5 - 81729198 81729197 81729198 TTCATAAAAATGAGTAAGTTTAACACTTTGAAAGTATTGAGAAATTGAGGACAGCATATTTATTT TTCATAAAAATGAGTAAGTTTAACACTTTGAA_GTATTGAGAAATTGAGGACAGCATATTTATTT CT C SSBP2 Ensembl:ENSG00000145687 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs572346312 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_232926,RMVar_hsa_circ_119581 14632 RMVar_ID_14632 Human_SNP_ID_238738944 A-to-I Human chr5 + 82021620 82021620 82021620 AAAATATTTTATCAGCCGGGCGTGGTGGCTCAAACCTGTAATCCCAGCACTTTGGGAAGCTGGGG AAAATATTTTATCAGCCGGGCGTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAAGCTGGGG A C ATG10 Ensembl:ENSG00000152348 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs562982777 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121266,RMVar_hsa_circ_232940,RMVar_hsa_circ_311896,RMVar_hsa_circ_232939,RMVar_hsa_circ_303117 14633 RMVar_ID_14633 Human_SNP_ID_238738945 A-to-I Human chr5 + 82021620 82021620 82021620 AAAATATTTTATCAGCCGGGCGTGGTGGCTCAAACCTGTAATCCCAGCACTTTGGGAAGCTGGGG AAAATATTTTATCAGCCGGGCGTGGTGGCTCATACCTGTAATCCCAGCACTTTGGGAAGCTGGGG A T ATG10 Ensembl:ENSG00000152348 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs562982777 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121266,RMVar_hsa_circ_232940,RMVar_hsa_circ_311896,RMVar_hsa_circ_232939,RMVar_hsa_circ_303117 14634 RMVar_ID_14634 Human_SNP_ID_238739195 A-to-I Human chr5 + 82022575 82022575 82022575 CAGCTCCTGACATGAGGTGATCCTCCTGCCTCAGCATCCCAAAGTGCTGGGATTACAGGTGTGAA CAGCTCCTGACATGAGGTGATCCTCCTGCCTCGGCATCCCAAAGTGCTGGGATTACAGGTGTGAA A G ATG10 Ensembl:ENSG00000152348 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs971647000 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121266,RMVar_hsa_circ_232940,RMVar_hsa_circ_311896,RMVar_hsa_circ_232939,RMVar_hsa_circ_303117 14635 RMVar_ID_14635 Human_SNP_ID_238748490 A-to-I Human chr5 + 82063041 82063041 82063041 TAGTTTTTCATTTTAAAATACCTCAGATGGCCAGGTATGGTGGCTCACACCTGTAATCCCAGTGC TAGTTTTTCATTTTAAAATACCTCAGATGGCCGGGTATGGTGGCTCACACCTGTAATCCCAGTGC A G ATG10 Ensembl:ENSG00000152348 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1039894701 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121266,RMVar_hsa_circ_232940,RMVar_hsa_circ_232939,RMVar_hsa_circ_303117,RMVar_hsa_circ_355139,RMVar_hsa_circ_125281,RMVar_hsa_circ_232942,RMVar_hsa_circ_232943 14636 RMVar_ID_14636 Human_SNP_ID_238801238 A-to-I Human chr5 + 82294610 82294610 82294610 GGGAGGTTGAGGCAAGAGAATCACTTGAACTCAGGAGGTTGAGATTGCAGTGAGCCGAGATCGCG GGGAGGTTGAGGCAAGAGAATCACTTGAACTCGGGAGGTTGAGATTGCAGTGAGCCGAGATCGCG A G ATP6AP1L Ensembl:ENSG00000205464 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs750597064 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_232950,RMVar_hsa_circ_289001,RMVar_hsa_circ_356423,RMVar_hsa_circ_43989 14637 RMVar_ID_14637 Human_SNP_ID_238801239 A-to-I Human chr5 + 82294610 82294610 82294610 GGGAGGTTGAGGCAAGAGAATCACTTGAACTCAGGAGGTTGAGATTGCAGTGAGCCGAGATCGCG GGGAGGTTGAGGCAAGAGAATCACTTGAACTCTGGAGGTTGAGATTGCAGTGAGCCGAGATCGCG A T ATP6AP1L Ensembl:ENSG00000205464 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs750597064 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_232950,RMVar_hsa_circ_289001,RMVar_hsa_circ_356423,RMVar_hsa_circ_43989 14638 RMVar_ID_14638 Human_SNP_ID_239008413 A-to-I Human chr5 + 83152449 83152449 83152449 AGGTCAGGGATTCGAGACTCAGCCTGACCAACATGGTGAAACCCTGTCTCGACTAAAAATACAAA AGGTCAGGGATTCGAGACTCAGCCTGACCAACGTGGTGAAACCCTGTCTCGACTAAAAATACAAA A G XRCC4 Ensembl:ENSG00000152422 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1462473373 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_302436,RMVar_hsa_circ_353399,RMVar_hsa_circ_8492 14639 RMVar_ID_14639 Human_SNP_ID_239215846 A-to-I Human chr5 - 84038088 84038088 84038088 TGAAGCACGAGAATTGCTTGAACCCGGGAGGCAGAGTTTGCAGTGAGCTGAGATCATGCCACTGC TGAAGCACGAGAATTGCTTGAACCCGGGAGGCGGAGTTTGCAGTGAGCTGAGATCATGCCACTGC T C EDIL3 Ensembl:ENSG00000164176 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1012542062 Functional Loss SNV dbSNP153 33..33 33 - - - 14640 RMVar_ID_14640 Human_SNP_ID_240029085 A-to-I Human chr5 + 87271024 87271015 87271024 ACTTCGGGAGGCCGAGGCGGGTGGATCACCTGAAGTCCGGAGTTTGAGACCAGCCTGACCGAGAT ACTTCGGGAGGCCGAGGCGGGTGG_________AGTCCGGAGTTTGAGACCAGCCTGACCGAGAT GATCACCTGA G RASA1 Ensembl:ENSG00000145715 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1376200028 Functional Loss DEL dbSNP153 25..33 33 - - - 14641 RMVar_ID_14641 Human_SNP_ID_240029332 A-to-I Human chr5 + 87271683 87271683 87271683 TTTCATATTTTTAGTAGAGACAGGGTTTTGCCATGTTGGCCAGGCTGGTCTCGAACTCTGACCTC TTTCATATTTTTAGTAGAGACAGGGTTTTGCCGTGTTGGCCAGGCTGGTCTCGAACTCTGACCTC A G RASA1 Ensembl:ENSG00000145715 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041728548 Functional Loss SNV dbSNP153 33..33 33 - - - 14642 RMVar_ID_14642 Human_SNP_ID_240029334 A-to-I Human chr5 + 87271692 87271692 87271692 TTTAGTAGAGACAGGGTTTTGCCATGTTGGCCAGGCTGGTCTCGAACTCTGACCTCAGGTGATCC TTTAGTAGAGACAGGGTTTTGCCATGTTGGCCGGGCTGGTCTCGAACTCTGACCTCAGGTGATCC A G RASA1 Ensembl:ENSG00000145715 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1230554598 Functional Loss SNV dbSNP153 33..33 33 - - - 14643 RMVar_ID_14643 Human_SNP_ID_240031538 A-to-I Human chr5 + 87280510 87280510 87280510 AATTCTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCCGGTCCTGAACTCCTGA AATTCTTGTATTTTTAGTAGAGACAGGGTTTCGCCATGTTGGCCAGGCCGGTCCTGAACTCCTGA A G RASA1 Ensembl:ENSG00000145715 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1479165342 Functional Loss SNV dbSNP153 33..33 33 - - - 14644 RMVar_ID_14644 Human_SNP_ID_240056489 A-to-I Human chr5 - 87382971 87382971 87382971 TCTCTTGCCTCAGGCTTAGAGTAGTTAGGACTACAGGTGCACATCACCATACCTGGCAATTTTTT TCTCTTGCCTCAGGCTTAGAGTAGTTAGGACTTCAGGTGCACATCACCATACCTGGCAATTTTTT T A CCNH Ensembl:ENSG00000134480 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1490514459 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15539010 14645 RMVar_ID_14645 Human_SNP_ID_240056497 A-to-I Human chr5 - 87383010 87383010 87383010 ACAGCTCACTGCAACCTTGAACCCCTGGGATCAAACAATTCTCTTGCCTCAGGCTTAGAGTAGTT ACAGCTCACTGCAACCTTGAACCCCTGGGATCGAACAATTCTCTTGCCTCAGGCTTAGAGTAGTT T C CCNH Ensembl:ENSG00000134480 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs778522858 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15539013,Human_RBP_ID_24120389 14646 RMVar_ID_14646 Human_SNP_ID_240056508 A-to-I Human chr5 - 87383088 87383088 87383088 TTTTTTCCTTTTTTCTTTGTTTTCTTTGAGATAGGGTTTTGTTCTGTCACCCAGGCTGGAGTGCA TTTTTTCCTTTTTTCTTTGTTTTCTTTGAGATGGGGTTTTGTTCTGTCACCCAGGCTGGAGTGCA T C CCNH Ensembl:ENSG00000134480 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs905349602 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15539020 14647 RMVar_ID_14647 Human_SNP_ID_240250042 A-to-I Human chr5 - 88186686 88186686 88186686 ACCTCAGCTAATCCACCTGCCTTGGCCTCCCAAATTCCTGGGATTACAGGTGTGAGCCACCGCAC ACCTCAGCTAATCCACCTGCCTTGGCCTCCCAGATTCCTGGGATTACAGGTGTGAGCCACCGCAC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs376335473 Functional Loss SNV dbSNP153 33..33 33 - - - 14648 RMVar_ID_14648 Human_SNP_ID_240250053 A-to-I Human chr5 - 88186738 88186738 88186738 TTTTTTAGTAGAGACGTTTCACCATTTTGGCCAGGCTGGTCTCGAACTTCTGACCTCAGCTAATC TTTTTTAGTAGAGACGTTTCACCATTTTGGCCCGGCTGGTCTCGAACTTCTGACCTCAGCTAATC T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs915684055 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15540270 14649 RMVar_ID_14649 Human_SNP_ID_240275990 A-to-I Human chr5 + 88296289 88296289 88296289 GCCAGGAGTTCAAGACTTGCCTGGCCATCTCTACTAAAAATACAAAAATTAGCCAGGCATGATGG GCCAGGAGTTCAAGACTTGCCTGGCCATCTCTGCTAAAAATACAAAAATTAGCCAGGCATGATGG A G TMEM161B-AS1 Ensembl:ENSG00000247828 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs184358398 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36934,RMVar_hsa_circ_233046,RMVar_hsa_circ_233050 14650 RMVar_ID_14650 Human_SNP_ID_240278279 A-to-I Human chr5 + 88305820 88305820 88305820 CTGCAGCTCCCAGCGTGATTGACGCAGAAGACAAGTGATTTCTGCATTTCTAACTGAGGTATCTG CTGCAGCTCCCAGCGTGATTGACGCAGAAGACCAGTGATTTCTGCATTTCTAACTGAGGTATCTG A C TMEM161B-AS1 Ensembl:ENSG00000247828 lincRNA intron GSE107867 ASD brains,cerebellum;ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1182874622 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36934,RMVar_hsa_circ_233046,RMVar_hsa_circ_233050 14651 RMVar_ID_14651 Human_SNP_ID_240280646 A-to-I Human chr5 + 88313959 88313939 88313960 TTCCCTGACCCATTGCACTTCCCGGGTGAGGCAATGCCTCACCCTGCTTCAGCTCATGCATGGTG TTCCCTGACCCAT_____________________TGCCTCACCCTGCTTCAGCTCATGCATGGTG TTGCACTTCCCGGGTGAGGCAA T TMEM161B-AS1 Ensembl:ENSG00000247828 lincRNA intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1561462523 Functional Loss DEL dbSNP153 14..34 33 - - - RMVar_hsa_circ_36934,RMVar_hsa_circ_233046,RMVar_hsa_circ_233050 14652 RMVar_ID_14652 Human_SNP_ID_667078100 A-to-I Human chr19 + 45012629 45012629 45012629 AGCCGAGTGTGGTGGCACAATCCCAGCTATTTAGGAGGCCGAGGTGGGAGGATTAGCTGAGCCCA AGCCGAGTGTGGTGGCACAATCCCAGCTATTTGGGAGGCCGAGGTGGGAGGATTAGCTGAGCCCA A G RELB Ensembl:ENSG00000104856 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1192542521 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34073,RMVar_hsa_circ_195266,RMVar_hsa_circ_111216,RMVar_hsa_circ_53840,RMVar_hsa_circ_362065,RMVar_hsa_circ_34429 14653 RMVar_ID_14653 Human_SNP_ID_667078181 A-to-I Human chr19 + 45012928 45012928 45012928 AAAATTAGCCAGGTGTGGTGGCACATGGCTGTAGTCCTAGCTACATGGTAGGGCTGAGGTGGGAG AAAATTAGCCAGGTGTGGTGGCACATGGCTGTGGTCCTAGCTACATGGTAGGGCTGAGGTGGGAG A G RELB Ensembl:ENSG00000104856 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1286083569 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34073,RMVar_hsa_circ_195266,RMVar_hsa_circ_111216,RMVar_hsa_circ_53840,RMVar_hsa_circ_362065,RMVar_hsa_circ_34429 14654 RMVar_ID_14654 Human_SNP_ID_667078195 A-to-I Human chr19 + 45012989 45012989 45012989 GGAGGATCGCTTGAGCCTAGGAGGTCAAGGCTACAGTGAGCCAAGATCGCACCACTGCACTCCAG GGAGGATCGCTTGAGCCTAGGAGGTCAAGGCTGCAGTGAGCCAAGATCGCACCACTGCACTCCAG A G RELB Ensembl:ENSG00000104856 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs144517084 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23310198 RMVar_hsa_circ_34073,RMVar_hsa_circ_195266,RMVar_hsa_circ_111216,RMVar_hsa_circ_53840,RMVar_hsa_circ_362065,RMVar_hsa_circ_34429 14655 RMVar_ID_14655 Human_SNP_ID_667078500 A-to-I Human chr19 + 45014287 45014287 45014287 CACCTCCCAGGCTCAAGAGACCCTCCCACCTCAGCCTCCTGAGTTGCTGGGACTACAGGTGCATG CACCTCCCAGGCTCAAGAGACCCTCCCACCTCGGCCTCCTGAGTTGCTGGGACTACAGGTGCATG A G RELB Ensembl:ENSG00000104856 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1381127147 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34073,RMVar_hsa_circ_195266,RMVar_hsa_circ_111216,RMVar_hsa_circ_53840,RMVar_hsa_circ_362065,RMVar_hsa_circ_34429 14656 RMVar_ID_14656 Human_SNP_ID_667078636 A-to-I Human chr19 + 45014780 45014780 45014780 ACCCCAAGTGATCTGTCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGTGC ACCCCAAGTGATCTGTCTGCCTCAGCCTCCCAGAGTGCTGGGATTACAGGTGTGAGCCACCGTGC A G RELB Ensembl:ENSG00000104856 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1359724041 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34073,RMVar_hsa_circ_195266,RMVar_hsa_circ_111216,RMVar_hsa_circ_53840,RMVar_hsa_circ_362065,RMVar_hsa_circ_34429 14657 RMVar_ID_14657 Human_SNP_ID_667078728 A-to-I Human chr19 + 45015164 45015164 45015164 CCCTCAGGTAATCCACCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCAGCATGC CCCTCAGGTAATCCACCTGCCTCGGCCTCCCAGAGTGCTGGGATTACAGGCATGAGCCAGCATGC A G RELB Ensembl:ENSG00000104856 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs142704517 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34073,RMVar_hsa_circ_195266,RMVar_hsa_circ_111216,RMVar_hsa_circ_53840,RMVar_hsa_circ_362065,RMVar_hsa_circ_34429 14658 RMVar_ID_14658 Human_SNP_ID_667078812 A-to-I Human chr19 + 45015588 45015588 45015588 AAGATGCCCGTCTCTATAAAAATAAAAAAATTAGCCAGGCGTGGTGGCATGCGCCTGGGGTCCCA AAGATGCCCGTCTCTATAAAAATAAAAAAATTGGCCAGGCGTGGTGGCATGCGCCTGGGGTCCCA A G RELB Ensembl:ENSG00000104856 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1032203233 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34073,RMVar_hsa_circ_195266,RMVar_hsa_circ_111216,RMVar_hsa_circ_53840,RMVar_hsa_circ_362065,RMVar_hsa_circ_34429 14659 RMVar_ID_14659 Human_SNP_ID_667079350 A-to-I Human chr19 + 45017749 45017749 45017749 AATGGTGCGATCTCTGCCTCTCAGGTTCAAGCAGTCCTCTTGCCTCAGCCTCCTGAGTTGGTAGG AATGGTGCGATCTCTGCCTCTCAGGTTCAAGCGGTCCTCTTGCCTCAGCCTCCTGAGTTGGTAGG A G RELB Ensembl:ENSG00000104856 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs550681960 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34073,RMVar_hsa_circ_195266,RMVar_hsa_circ_111216,RMVar_hsa_circ_53840,RMVar_hsa_circ_362065,RMVar_hsa_circ_34429 14660 RMVar_ID_14660 Human_SNP_ID_667079512 A-to-I Human chr19 + 45018473 45018473 45018473 AGGCATGGTGGCAGGCACCTGTAATCTTAGCTACTTAGAAGGTAGAGACGAGAATGGCTTGAACC AGGCATGGTGGCAGGCACCTGTAATCTTAGCTTCTTAGAAGGTAGAGACGAGAATGGCTTGAACC A T RELB Ensembl:ENSG00000104856 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs981754233 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34073,RMVar_hsa_circ_195266,RMVar_hsa_circ_111216,RMVar_hsa_circ_53840,RMVar_hsa_circ_362065,RMVar_hsa_circ_34429 14661 RMVar_ID_14661 Human_SNP_ID_667079784 A-to-I Human chr19 + 45019699 45019696 45019699 TTATGTATTTATGTATTTATTTATTTTTTGAGAAGGAGTCTTGCTTTGTCACCCAGGCTGGAGTG TTATGTATTTATGTATTTATTTATTTTTTG___AGGAGTCTTGCTTTGTCACCCAGGCTGGAGTG GAGA G RELB Ensembl:ENSG00000104856 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1568400723 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_13473172 RMVar_hsa_circ_34073,RMVar_hsa_circ_195266,RMVar_hsa_circ_111216,RMVar_hsa_circ_53840,RMVar_hsa_circ_362065,RMVar_hsa_circ_34429 14662 RMVar_ID_14662 Human_SNP_ID_667079820 A-to-I Human chr19 + 45019851 45019851 45019851 AGGCATGTGCCACCACGTGCGGCTAATTTTGTATTTTTAGTAGAGACGGTGTTTCTCCATGTTGG AGGCATGTGCCACCACGTGCGGCTAATTTTGTGTTTTTAGTAGAGACGGTGTTTCTCCATGTTGG A G RELB Ensembl:ENSG00000104856 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1341988847 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34073,RMVar_hsa_circ_195266,RMVar_hsa_circ_111216,RMVar_hsa_circ_53840,RMVar_hsa_circ_362065,RMVar_hsa_circ_34429 14663 RMVar_ID_14663 Human_SNP_ID_667079976 A-to-I Human chr19 + 45020398 45020398 45020398 GATGCCTGTCACCACACCTGGCTAATTTTTGTATTTTTTATAGAGACGGGGTTGCCCAGGCTGGT GATGCCTGTCACCACACCTGGCTAATTTTTGTGTTTTTTATAGAGACGGGGTTGCCCAGGCTGGT A G RELB Ensembl:ENSG00000104856 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1293626160 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34073,RMVar_hsa_circ_195266,RMVar_hsa_circ_111216,RMVar_hsa_circ_53840,RMVar_hsa_circ_362065,RMVar_hsa_circ_34429 14664 RMVar_ID_14664 Human_SNP_ID_667080247 A-to-I Human chr19 + 45021151 45021151 45021151 AGCTGAGATCTCCCGCCACCGCACTCTAGCTTAGGTGATACAGCGAGACCCTGTCACAAAAAAAT AGCTGAGATCTCCCGCCACCGCACTCTAGCTTCGGTGATACAGCGAGACCCTGTCACAAAAAAAT A C RELB Ensembl:ENSG00000104856 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1342691904 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34073,RMVar_hsa_circ_195266,RMVar_hsa_circ_111216,RMVar_hsa_circ_53840,RMVar_hsa_circ_362065,RMVar_hsa_circ_34429 14665 RMVar_ID_14665 Human_SNP_ID_667080462 A-to-I Human chr19 + 45021668 45021668 45021668 AAGAACTCGGCTCACTGCATCCTCCGCCTCCCAGGTTCAGGCGATTCTCCTGCCTCAGCCTCCCG AAGAACTCGGCTCACTGCATCCTCCGCCTCCCTGGTTCAGGCGATTCTCCTGCCTCAGCCTCCCG A T RELB Ensembl:ENSG00000104856 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1159492219 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34073,RMVar_hsa_circ_195266,RMVar_hsa_circ_111216,RMVar_hsa_circ_53840,RMVar_hsa_circ_362065,RMVar_hsa_circ_34429 14666 RMVar_ID_14666 Human_SNP_ID_667080467 A-to-I Human chr19 + 45021692 45021692 45021692 CGCCTCCCAGGTTCAGGCGATTCTCCTGCCTCAGCCTCCCGAGCAGGTGGGATTACAGGCATGCG CGCCTCCCAGGTTCAGGCGATTCTCCTGCCTCGGCCTCCCGAGCAGGTGGGATTACAGGCATGCG A G RELB Ensembl:ENSG00000104856 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs908120258 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34073,RMVar_hsa_circ_195266,RMVar_hsa_circ_111216,RMVar_hsa_circ_53840,RMVar_hsa_circ_362065,RMVar_hsa_circ_34429 14667 RMVar_ID_14667 Human_SNP_ID_667083075 A-to-I Human chr19 + 45031314 45031314 45031314 CCTGGCTAATTTTTTAATTTTCTTGTAGAGACAAGGTCTTGCTGTGTTGGCCAGTCTGGTCTTGA CCTGGCTAATTTTTTAATTTTCTTGTAGAGACGAGGTCTTGCTGTGTTGGCCAGTCTGGTCTTGA A G RELB Ensembl:ENSG00000104856 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs979104285 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34073,RMVar_hsa_circ_119053,RMVar_hsa_circ_40758,RMVar_hsa_circ_332495,RMVar_hsa_circ_361060,RMVar_hsa_circ_195273 14668 RMVar_ID_14668 Human_SNP_ID_667083885 A-to-I Human chr19 + 45034012 45034012 45034012 AATCCCATCTCTACTAAAAAAATACAAAAATTAGCTGGGCGTGGTGGCGCACACCTGTAATCCCT AATCCCATCTCTACTAAAAAAATACAAAAATTTGCTGGGCGTGGTGGCGCACACCTGTAATCCCT A T RELB Ensembl:ENSG00000104856 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1257170827 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_361060 14669 RMVar_ID_14669 Human_SNP_ID_667085781 A-to-I Human chr19 + 45040808 45040808 45040808 CAAAAGGGTGAAACCCCATCTCTACTAAAGATACAAAAATTAGCCAGGCTTAGTGGTGTGTGCAT CAAAAGGGTGAAACCCCATCTCTACTAAAGATGCAAAAATTAGCCAGGCTTAGTGGTGTGTGCAT A G CLASRP Ensembl:ENSG00000104859 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1333009495 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100916,RMVar_hsa_circ_375852,RMVar_hsa_circ_195276,RMVar_hsa_circ_195277 14670 RMVar_ID_14670 Human_SNP_ID_667086293 A-to-I Human chr19 + 45042706 45042706 45042706 ATGATGTCAGCTCACTGTAACGTCCACCCCCCAGGTTCAAGCTATTCTCCTGCCTCACTCAACCT ATGATGTCAGCTCACTGTAACGTCCACCCCCCGGGTTCAAGCTATTCTCCTGCCTCACTCAACCT A G CLASRP Ensembl:ENSG00000104859 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1365296036 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100916,RMVar_hsa_circ_375852,RMVar_hsa_circ_195276,RMVar_hsa_circ_195277 14671 RMVar_ID_14671 Human_SNP_ID_667086914 A-to-I Human chr19 + 45044701 45044701 45044701 TGAGGCAAGATGAGACCTGGGAGGGTGGGGCTACAGTGAGCTGTGATTGCACCACTGCACTGGAA TGAGGCAAGATGAGACCTGGGAGGGTGGGGCTGCAGTGAGCTGTGATTGCACCACTGCACTGGAA A G CLASRP Ensembl:ENSG00000104859 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1186122643 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17568114 RMVar_hsa_circ_100916,RMVar_hsa_circ_375852,RMVar_hsa_circ_195276,RMVar_hsa_circ_195277 14672 RMVar_ID_14672 Human_SNP_ID_667087036 A-to-I Human chr19 + 45045238 45045238 45045238 CTCATGCCATTTGTTGAGAAAGTTTCTAGGCCAGGTGCAGTGGCTCACGCCTGTAATCCCAGCAC CTCATGCCATTTGTTGAGAAAGTTTCTAGGCCGGGTGCAGTGGCTCACGCCTGTAATCCCAGCAC A G CLASRP Ensembl:ENSG00000104859 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1173714524 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13473272 RMVar_hsa_circ_100916,RMVar_hsa_circ_375852,RMVar_hsa_circ_195276,RMVar_hsa_circ_195277 14673 RMVar_ID_14673 Human_SNP_ID_667088509 A-to-I Human chr19 + 45051362 45051362 45051362 TTGAGATGGAGTCTTGCTCTGTTGCCCAGGCTAGAGTGCGGTGACACAATCTCAGCTCACTGCAA TTGAGATGGAGTCTTGCTCTGTTGCCCAGGCTGGAGTGCGGTGACACAATCTCAGCTCACTGCAA A G CLASRP Ensembl:ENSG00000104859 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1455324673 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17567734,Human_RBP_ID_22477235 RMVar_hsa_circ_100916,RMVar_hsa_circ_375852,RMVar_hsa_circ_195276,RMVar_hsa_circ_195277 14674 RMVar_ID_14674 Human_SNP_ID_667088520 A-to-I Human chr19 + 45051383 45051383 45051383 TTGCCCAGGCTAGAGTGCGGTGACACAATCTCAGCTCACTGCAACTTCTGCCTCCCAGGTTCAAG TTGCCCAGGCTAGAGTGCGGTGACACAATCTCGGCTCACTGCAACTTCTGCCTCCCAGGTTCAAG A G CLASRP Ensembl:ENSG00000104859 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs910973553 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100916,RMVar_hsa_circ_375852,RMVar_hsa_circ_195276,RMVar_hsa_circ_195277 14675 RMVar_ID_14675 Human_SNP_ID_667088521 A-to-I Human chr19 + 45051383 45051383 45051383 TTGCCCAGGCTAGAGTGCGGTGACACAATCTCAGCTCACTGCAACTTCTGCCTCCCAGGTTCAAG TTGCCCAGGCTAGAGTGCGGTGACACAATCTCTGCTCACTGCAACTTCTGCCTCCCAGGTTCAAG A T CLASRP Ensembl:ENSG00000104859 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs910973553 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100916,RMVar_hsa_circ_375852,RMVar_hsa_circ_195276,RMVar_hsa_circ_195277 14676 RMVar_ID_14676 Human_SNP_ID_667092926 A-to-I Human chr19 + 45066219 45066219 45066219 CTCGGCTCACTGCACCTCCTCCTCCTGGGTTCAAGTGATTCTCCCGCCGCAGCCTCCCAAGTAGC CTCGGCTCACTGCACCTCCTCCTCCTGGGTTCCAGTGATTCTCCCGCCGCAGCCTCCCAAGTAGC A C CLASRP Ensembl:ENSG00000104859 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417035438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25424696 RMVar_hsa_circ_100916,RMVar_hsa_circ_195276 14677 RMVar_ID_14677 Human_SNP_ID_667092935 A-to-I Human chr19 + 45066245 45066245 45066245 GGGTTCAAGTGATTCTCCCGCCGCAGCCTCCCAAGTAGCTGGGATTACAGGCATGCGCCACCACA GGGTTCAAGTGATTCTCCCGCCGCAGCCTCCCGAGTAGCTGGGATTACAGGCATGCGCCACCACA A G CLASRP Ensembl:ENSG00000104859 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1354974233 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100916,RMVar_hsa_circ_195276 14678 RMVar_ID_14678 Human_SNP_ID_667092941 A-to-I Human chr19 + 45066265 45066265 45066265 CCGCAGCCTCCCAAGTAGCTGGGATTACAGGCATGCGCCACCACACCTGGCTAATTTTTGTATTT CCGCAGCCTCCCAAGTAGCTGGGATTACAGGCCTGCGCCACCACACCTGGCTAATTTTTGTATTT A C CLASRP Ensembl:ENSG00000104859 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1430523489 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100916,RMVar_hsa_circ_195276 14679 RMVar_ID_14679 Human_SNP_ID_667097826 A-to-I Human chr19 + 45081280 45081280 45081280 GGAGTTTGAGACCAGCCTGGCCAACGTGGCCAAACCGCGTCTCTACTAAAAATACAAAATTAGCC GGAGTTTGAGACCAGCCTGGCCAACGTGGCCAGACCGCGTCTCTACTAAAAATACAAAATTAGCC A G MARK4,GEMIN7 Ensembl:ENSG00000007047,Ensembl:ENSG00000142252 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1289100456 Functional Loss SNV dbSNP153 33..33 33 - - - 14680 RMVar_ID_14680 Human_SNP_ID_667097963 A-to-I Human chr19 + 45081756 45081756 45081756 TCAAGCGATTCTTCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCACGCACCACCACACCCA TCAAGCGATTCTTCTGCCTCAGCCTCCCGAGTGGCTGGGATTACAGGCACGCACCACCACACCCA A G MARK4,GEMIN7 Ensembl:ENSG00000007047,Ensembl:ENSG00000142252 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1011147130 Functional Loss SNV dbSNP153 33..33 33 - - - 14681 RMVar_ID_14681 Human_SNP_ID_667098165 A-to-I Human chr19 + 45082596 45082595 45082596 GCACAGAGCAGGCACTCAGATGATGTGCTAACAATGCTAGATAATGTGGATGAGTGAATTTTTTT GCACAGAGCAGGCACTCAGATGATGTGCTAATGATGCTAGATAATGTGGATGAGTGAATTTTTTT CA TG MARK4,GEMIN7 Ensembl:ENSG00000007047,Ensembl:ENSG00000142252 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs386809719 Functional Loss MNV dbSNP153 32..33 33 - - - 14682 RMVar_ID_14682 Human_SNP_ID_667098167 A-to-I Human chr19 + 45082596 45082596 45082596 GCACAGAGCAGGCACTCAGATGATGTGCTAACAATGCTAGATAATGTGGATGAGTGAATTTTTTT GCACAGAGCAGGCACTCAGATGATGTGCTAACGATGCTAGATAATGTGGATGAGTGAATTTTTTT A G MARK4,GEMIN7 Ensembl:ENSG00000007047,Ensembl:ENSG00000142252 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10414406 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_1138 14683 RMVar_ID_14683 Human_SNP_ID_667098168 A-to-I Human chr19 + 45082596 45082596 45082596 GCACAGAGCAGGCACTCAGATGATGTGCTAACAATGCTAGATAATGTGGATGAGTGAATTTTTTT GCACAGAGCAGGCACTCAGATGATGTGCTAACTATGCTAGATAATGTGGATGAGTGAATTTTTTT A T MARK4,GEMIN7 Ensembl:ENSG00000007047,Ensembl:ENSG00000142252 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10414406 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_1138 14684 RMVar_ID_14684 Human_SNP_ID_667098181 A-to-I Human chr19 + 45082640 45082640 45082640 TGTGGATGAGTGAATTTTTTTTTTTTTGAGACAGGGTCTCATACTCTGTCACCCAGGCTGGAGTA TGTGGATGAGTGAATTTTTTTTTTTTTGAGACGGGGTCTCATACTCTGTCACCCAGGCTGGAGTA A G MARK4,GEMIN7 Ensembl:ENSG00000007047,Ensembl:ENSG00000142252 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1389993067 Functional Loss SNV dbSNP153 33..33 33 - - - 14685 RMVar_ID_14685 Human_SNP_ID_667098463 A-to-I Human chr19 + 45083634 45083630 45083634 TTTTTTTTTTTTTTTGTTTGAGACAGGGTCTCACTCTTCCCAGGCTGGAGTGCAGTGGTGCAATC TTTTTTTTTTTTTTTGTTTGAGACAGGGT____CTCTTCCCAGGCTGGAGTGCAGTGGTGCAATC TCTCA T MARK4,GEMIN7 Ensembl:ENSG00000007047,Ensembl:ENSG00000142252 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1201883496 Functional Loss DEL dbSNP153 30..33 33 - - - 14686 RMVar_ID_14686 Human_SNP_ID_667098806 A-to-I Human chr19 + 45084833 45084833 45084833 GCTGGAGCGCAATGGCGCAGTCTCGGCTCACCACAACCTCTGCCTCCTGAGTTCAAGTGATTCTC GCTGGAGCGCAATGGCGCAGTCTCGGCTCACCGCAACCTCTGCCTCCTGAGTTCAAGTGATTCTC A G MARK4,GEMIN7 Ensembl:ENSG00000007047,Ensembl:ENSG00000142252 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4803797 Functional Loss SNV dbSNP153 33..33 33 - - - 14687 RMVar_ID_14687 Human_SNP_ID_667098817 A-to-I Human chr19 + 45084881 45084881 45084881 GAGTTCAAGTGATTCTCCTGCTTCAGCCTTCCAAGTAGCTGGGATTACAGGCATGCACCACCACT GAGTTCAAGTGATTCTCCTGCTTCAGCCTTCCGAGTAGCTGGGATTACAGGCATGCACCACCACT A G MARK4,GEMIN7 Ensembl:ENSG00000007047,Ensembl:ENSG00000142252 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7246952 Functional Loss SNV dbSNP153 33..33 33 - - - 14688 RMVar_ID_14688 Human_SNP_ID_667098818 A-to-I Human chr19 + 45084881 45084881 45084881 GAGTTCAAGTGATTCTCCTGCTTCAGCCTTCCAAGTAGCTGGGATTACAGGCATGCACCACCACT GAGTTCAAGTGATTCTCCTGCTTCAGCCTTCCTAGTAGCTGGGATTACAGGCATGCACCACCACT A T MARK4,GEMIN7 Ensembl:ENSG00000007047,Ensembl:ENSG00000142252 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7246952 Functional Loss SNV dbSNP153 33..33 33 - - - 14689 RMVar_ID_14689 Human_SNP_ID_667099043 A-to-I Human chr19 + 45085785 45085785 45085785 CCTGACCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAAGTAGCTGGGCATGGTGGTGT CCTGACCAACATGGTGAAACCCCGTCTCTACTGAAAATACAAAAAGTAGCTGGGCATGGTGGTGT A G MARK4,GEMIN7 Ensembl:ENSG00000007047,Ensembl:ENSG00000142252 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1195442306 Functional Loss SNV dbSNP153 33..33 33 - - - 14690 RMVar_ID_14690 Human_SNP_ID_667101704 A-to-I Human chr19 + 45094173 45094173 45094173 TGTGGTTTTTATGTTTTCTTTTTTATTGAGACAAGGTCTCACTACATTGCCCAGGCTGGTCTCGG TGTGGTTTTTATGTTTTCTTTTTTATTGAGACCAGGTCTCACTACATTGCCCAGGCTGGTCTCGG A C MARK4,PPP1R37 Ensembl:ENSG00000007047,Ensembl:ENSG00000104866 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs963556016 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267348 14691 RMVar_ID_14691 Human_SNP_ID_667102044 A-to-I Human chr19 + 45095398 45095398 45095398 ACCTCAGGTGATCTGCCCACTTAAGCCTTCCAAAGTGCTGGGATTACCGGCATGAGCCACCGTGC ACCTCAGGTGATCTGCCCACTTAAGCCTTCCACAGTGCTGGGATTACCGGCATGAGCCACCGTGC A C MARK4,PPP1R37 Ensembl:ENSG00000007047,Ensembl:ENSG00000104866 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1036187771 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267348 14692 RMVar_ID_14692 Human_SNP_ID_667102045 A-to-I Human chr19 + 45095398 45095398 45095398 ACCTCAGGTGATCTGCCCACTTAAGCCTTCCAAAGTGCTGGGATTACCGGCATGAGCCACCGTGC ACCTCAGGTGATCTGCCCACTTAAGCCTTCCAGAGTGCTGGGATTACCGGCATGAGCCACCGTGC A G MARK4,PPP1R37 Ensembl:ENSG00000007047,Ensembl:ENSG00000104866 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1036187771 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267348 14693 RMVar_ID_14693 Human_SNP_ID_667105460 A-to-I Human chr19 + 45108303 45108303 45108303 GTGATCTTGGCTGACTGCAAACTCCACCTCCTAGGCTCAAGCCATTCTCCTGCCTTAGCCTCCCG GTGATCTTGGCTGACTGCAAACTCCACCTCCTGGGCTCAAGCCATTCTCCTGCCTTAGCCTCCCG A G MARK4,PPP1R37 Ensembl:ENSG00000007047,Ensembl:ENSG00000104866 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1018409328 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13474167 RMVar_hsa_circ_267348 14694 RMVar_ID_14694 Human_SNP_ID_667111038 A-to-I Human chr19 + 45129499 45129499 45129499 TTTTGTATTTTTAGTAGAGACAGGGTTTCACTATGTTGGCCAGGCTGGTCTTGAACTCCTGACCT TTTTGTATTTTTAGTAGAGACAGGGTTTCACTGTGTTGGCCAGGCTGGTCTTGAACTCCTGACCT A G MARK4,PPP1R37 Ensembl:ENSG00000007047,Ensembl:ENSG00000104866 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1014936427 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267348 14695 RMVar_ID_14695 Human_SNP_ID_667122819 A-to-I Human chr19 - 45167886 45167886 45167886 TCAGATGATCCTCCTGCCTCAGCTTCCCAAGTAGCTGGGACACGGGTGCATGCCACCACACCTGG TCAGATGATCCTCCTGCCTCAGCTTCCCAAGTGGCTGGGACACGGGTGCATGCCACCACACCTGG T C TRAPPC6A Ensembl:ENSG00000007255 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs527988751 Functional Loss SNV dbSNP153 33..33 33 - - - 14696 RMVar_ID_14696 Human_SNP_ID_667124950 A-to-I Human chr19 - 45176133 45176133 45176133 TTAAAATTAGCTGGGCGTGATGACACATGCCTATACTACCAAGAACTCGGGAGGCTGAGGTGGGA TTAAAATTAGCTGGGCGTGATGACACATGCCTGTACTACCAAGAACTCGGGAGGCTGAGGTGGGA T C TRAPPC6A Ensembl:ENSG00000007255 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928234427 Functional Loss SNV dbSNP153 33..33 33 - - - 14697 RMVar_ID_14697 Human_SNP_ID_667125360 A-to-I Human chr19 - 45177257 45177257 45177257 GTGATTCTCCCGCCTGGGCCTCCCAAAGTGCTAGGATTACAGGCGTGAACTACCGTGACTGGCCC GTGATTCTCCCGCCTGGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAACTACCGTGACTGGCCC T C TRAPPC6A Ensembl:ENSG00000007255 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256011442 Functional Loss SNV dbSNP153 33..33 33 - - - 14698 RMVar_ID_14698 Human_SNP_ID_667146789 A-to-I Human chr19 + 45254932 45254932 45254932 CTTTGTAGAAATGGTTCATGACCCAGCGTGGTAGCTCACACCTATAATCCCAGAACTTTGGGAGA CTTTGTAGAAATGGTTCATGACCCAGCGTGGTGGCTCACACCTATAATCCCAGAACTTTGGGAGA A G MARK4 Ensembl:ENSG00000007047 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1052245914 Functional Loss SNV dbSNP153 33..33 33 - - - 14699 RMVar_ID_14699 Human_SNP_ID_667150629 A-to-I Human chr19 + 45268461 45268461 45268461 CAAAAATTAGGTGGTCGTTGTGGCGCGTGCCTATAATTCCAGCTGCTTGAGAGGCTGAGACATGA CAAAAATTAGGTGGTCGTTGTGGCGCGTGCCTGTAATTCCAGCTGCTTGAGAGGCTGAGACATGA A G MARK4 Ensembl:ENSG00000007047 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs762764692 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93983,RMVar_hsa_circ_288821,RMVar_hsa_circ_322217,RMVar_hsa_circ_195296,RMVar_hsa_circ_345827,RMVar_hsa_circ_267826,RMVar_hsa_circ_195306,RMVar_hsa_circ_114875,RMVar_hsa_circ_195298,RMVar_hsa_circ_195297,RMVar_hsa_circ_264951,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_195305,RMVar_hsa_circ_195310 14700 RMVar_ID_14700 Human_SNP_ID_667153556 A-to-I Human chr19 + 45278963 45278963 45278963 AAGAGAGACCAGGCGAGGTGGTTCATGCTGGTAATCCCAGCACTTTGGGAGGTCGAGGTAGAAGA AAGAGAGACCAGGCGAGGTGGTTCATGCTGGTGATCCCAGCACTTTGGGAGGTCGAGGTAGAAGA A G MARK4 Ensembl:ENSG00000007047 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs557822454 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93983,RMVar_hsa_circ_345827,RMVar_hsa_circ_9377,RMVar_hsa_circ_195306,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_195311,RMVar_hsa_circ_79500,RMVar_hsa_circ_26071,RMVar_hsa_circ_195310,RMVar_hsa_circ_349431,RMVar_hsa_circ_195317,RMVar_hsa_circ_101057,RMVar_hsa_circ_273685,RMVar_hsa_circ_304047,RMVar_hsa_circ_375992,RMVar_hsa_circ_121313,RMVar_hsa_circ_21080,RMVar_hsa_circ_195318,RMVar_hsa_circ_195315,RMVar_hsa_circ_195316,RMVar_hsa_circ_312187,RMVar_hsa_circ_195319 14701 RMVar_ID_14701 Human_SNP_ID_667156815 A-to-I Human chr19 + 45290305 45290305 45290305 GTAGGGGTGTTTCTCCAGAGGTCCTGACCATCAGGAGGCACCCAGCCGTGGTGGCTGGTGGTGTC GTAGGGGTGTTTCTCCAGAGGTCCTGACCATCGGGAGGCACCCAGCCGTGGTGGCTGGTGGTGTC A G MARK4 Ensembl:ENSG00000007047 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs896832984 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93983,RMVar_hsa_circ_9377,RMVar_hsa_circ_114875,RMVar_hsa_circ_195297,RMVar_hsa_circ_195308,RMVar_hsa_circ_83144,RMVar_hsa_circ_195309,RMVar_hsa_circ_195317,RMVar_hsa_circ_375992,RMVar_hsa_circ_121313,RMVar_hsa_circ_195318,RMVar_hsa_circ_42346 14702 RMVar_ID_14702 Human_SNP_ID_667179952 A-to-I Human chr19 - 45359899 45359899 45359899 GTGGTGGCACGCACCTATAGTTCCAACTACTCAGGAGCCTGAGACAGGAGAATTGCTTGAACCCG GTGGTGGCACGCACCTATAGTTCCAACTACTCGGGAGCCTGAGACAGGAGAATTGCTTGAACCCG T C ERCC2 Ensembl:ENSG00000104884 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1411212570 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25425016 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 14703 RMVar_ID_14703 Human_SNP_ID_667182433 A-to-I Human chr19 - 45367154 45367154 45367154 TTGTGTGTTTTTAGTAGAGACGGTGTTTCACCATGTTGGTTAGGCTGGTCTCTAACTCCCGACCT TTGTGTGTTTTTAGTAGAGACGGTGTTTCACCTTGTTGGTTAGGCTGGTCTCTAACTCCCGACCT T A ERCC2 Ensembl:ENSG00000104884 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs369281985 Functional Loss SNV dbSNP153 33..33 33 - - - 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 14704 RMVar_ID_14704 Human_SNP_ID_667186489 A-to-I Human chr19 - 45380601 45380601 45380601 GTTGACCAGGCTTGTCTTGAACTCCTGAGCTCAGGTCATCCACCCACCTCGGCCTCCCAAACTGC GTTGACCAGGCTTGTCTTGAACTCCTGAGCTCTGGTCATCCACCCACCTCGGCCTCCCAAACTGC T A PPP1R13L Ensembl:ENSG00000104881 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170516041 Functional Loss SNV dbSNP153 33..33 33 - - - 14705 RMVar_ID_14705 Human_SNP_ID_667186501 A-to-I Human chr19 - 45380646 45380646 45380646 CCCAGCTAATTTTTTGTGTTTTTAGTAGAGACAGGGTCTCGTCATGTTGACCAGGCTTGTCTTGA CCCAGCTAATTTTTTGTGTTTTTAGTAGAGACGGGGTCTCGTCATGTTGACCAGGCTTGTCTTGA T C PPP1R13L Ensembl:ENSG00000104881 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs867383654 Functional Loss SNV dbSNP153 33..33 33 - - - 14706 RMVar_ID_14706 Human_SNP_ID_667190250 A-to-I Human chr19 - 45393123 45393123 45393123 GTGGTGCAGTGGTGCAATCTCGGCTCACTGCAACCTCCGCCTCCTGGGTTCAAGCGATTCCTGTG GTGGTGCAGTGGTGCAATCTCGGCTCACTGCAGCCTCCGCCTCCTGGGTTCAAGCGATTCCTGTG T C PPP1R13L Ensembl:ENSG00000104881 Protein coding exon GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1030940079 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12194,RMVar_hsa_circ_105334,RMVar_hsa_circ_195339 14707 RMVar_ID_14707 Human_SNP_ID_667190270 A-to-I Human chr19 - 45393180 45393180 45393180 GTGTATATATATATATTTTGAGATGAAATCTCACTCTTTTGCCCAGGCTGGAGTGCAGTGGTGCA GTGTATATATATATATTTTGAGATGAAATCTCCCTCTTTTGCCCAGGCTGGAGTGCAGTGGTGCA T G PPP1R13L Ensembl:ENSG00000104881 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs927338613 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12194,RMVar_hsa_circ_105334,RMVar_hsa_circ_195339 14708 RMVar_ID_14708 Human_SNP_ID_667190271 A-to-I Human chr19 - 45393185 45393185 45393185 TGTGTGTGTATATATATATATTTTGAGATGAAATCTCACTCTTTTGCCCAGGCTGGAGTGCAGTG TGTGTGTGTATATATATATATTTTGAGATGAACTCTCACTCTTTTGCCCAGGCTGGAGTGCAGTG T G PPP1R13L Ensembl:ENSG00000104881 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1433229758 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12194,RMVar_hsa_circ_105334,RMVar_hsa_circ_195339 14709 RMVar_ID_14709 Human_SNP_ID_667190378 A-to-I Human chr19 - 45393509 45393509 45393509 CAGCTCACTGCATCCTACACCTCCCAGGTTCAAGCGATTCTCCTACCTCAGCTTCCCAAGTAGCT CAGCTCACTGCATCCTACACCTCCCAGGTTCAGGCGATTCTCCTACCTCAGCTTCCCAAGTAGCT T C PPP1R13L Ensembl:ENSG00000104881 Protein coding intron GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs1313175025 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23801208 RMVar_hsa_circ_12194,RMVar_hsa_circ_105334,RMVar_hsa_circ_195339 14710 RMVar_ID_14710 Human_SNP_ID_667190379 A-to-I Human chr19 - 45393510 45393510 45393510 TCAGCTCACTGCATCCTACACCTCCCAGGTTCAAGCGATTCTCCTACCTCAGCTTCCCAAGTAGC TCAGCTCACTGCATCCTACACCTCCCAGGTTCGAGCGATTCTCCTACCTCAGCTTCCCAAGTAGC T C PPP1R13L Ensembl:ENSG00000104881 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs375657653 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23801208 RMVar_hsa_circ_12194,RMVar_hsa_circ_105334,RMVar_hsa_circ_195339 14711 RMVar_ID_14711 Human_SNP_ID_667190495 A-to-I Human chr19 - 45393903 45393903 45393903 GTATGTGTGTGTGTTTTGGGGTTTATTTATTTATTTATTTTTGAGACAGAGTTTCACTCTTTTTT GTATGTGTGTGTGTTTTGGGGTTTATTTATTTTTTTATTTTTGAGACAGAGTTTCACTCTTTTTT T A PPP1R13L Ensembl:ENSG00000104881 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968742004 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23801209 RMVar_hsa_circ_12194,RMVar_hsa_circ_105334,RMVar_hsa_circ_195339 14712 RMVar_ID_14712 Human_SNP_ID_667190586 A-to-I Human chr19 - 45394283 45394283 45394283 AATAAAAGTACAAAAAATCTGCCGGGCATGGTAGTGGGCGCCTGTAGTCCCAGCTACTCAGGATG AATAAAAGTACAAAAAATCTGCCGGGCATGGTGGTGGGCGCCTGTAGTCCCAGCTACTCAGGATG T C PPP1R13L Ensembl:ENSG00000104881 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs951517199 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12194,RMVar_hsa_circ_105334,RMVar_hsa_circ_195339 14713 RMVar_ID_14713 Human_SNP_ID_667190620 A-to-I Human chr19 - 45394439 45394438 45394439 ATAGTAAGCTATCAATAGCTACCATATTAGCCAGGCACCGTGGCTCACCCTTGTAATCCTAGCAG ATAGTAAGCTATCAATAGCTACCATATTAGCC_GGCACCGTGGCTCACCCTTGTAATCCTAGCAG CT C PPP1R13L Ensembl:ENSG00000104881 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1303144201 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_12194,RMVar_hsa_circ_105334,RMVar_hsa_circ_195339 14714 RMVar_ID_14714 Human_SNP_ID_667190631 A-to-I Human chr19 - 45394519 45394519 45394519 AGATCATGCCACTGCACTCCAGCACAGGTGACAGGGTGAGACTCTGTCTCAAAAATAAATAAATA AGATCATGCCACTGCACTCCAGCACAGGTGACGGGGTGAGACTCTGTCTCAAAAATAAATAAATA T C PPP1R13L Ensembl:ENSG00000104881 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs920286660 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12194,RMVar_hsa_circ_105334,RMVar_hsa_circ_195339 14715 RMVar_ID_14715 Human_SNP_ID_667196595 A-to-I Human chr19 - 45412219 45412217 45412219 GGGAGACGGAGGTTGCAGTGAGCTGAAATCACACCACTGCCCTCCAGCCTGGACAACAGAAGCAA GGGAGACGGAGGTTGCAGTGAGCTGAAATCAC__CACTGCCCTCCAGCCTGGACAACAGAAGCAA GGT G ERCC1 Ensembl:ENSG00000012061 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335469498 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_378421,RMVar_hsa_circ_195345,RMVar_hsa_circ_94010,RMVar_hsa_circ_101592,RMVar_hsa_circ_77741,RMVar_hsa_circ_195346,RMVar_hsa_circ_195343,RMVar_hsa_circ_195344 14716 RMVar_ID_14716 Human_SNP_ID_667198232 A-to-I Human chr19 - 45418302 45418302 45418302 CTCTTTCGCCCAGACTGGAGTGTAGTGGTGCAATCTTGGCTCACTGCAACCTCCACCTCCTGGAT CTCTTTCGCCCAGACTGGAGTGTAGTGGTGCAGTCTTGGCTCACTGCAACCTCCACCTCCTGGAT T C ERCC1 Ensembl:ENSG00000012061 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1192449349 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73179,RMVar_hsa_circ_122004,RMVar_hsa_circ_195351,RMVar_hsa_circ_17110,RMVar_hsa_circ_332571,RMVar_hsa_circ_69115,RMVar_hsa_circ_195353 14717 RMVar_ID_14717 Human_SNP_ID_667217470 A-to-I Human chr19 - 45487182 45487182 45487182 AAAACTAGCCAGGTGTGGTGGCACACACCTATAGTCCCAGTTACTCTGAAAGCTGAAGCAAGAGG AAAACTAGCCAGGTGTGGTGGCACACACCTATGGTCCCAGTTACTCTGAAAGCTGAAGCAAGAGG T C RTN2 Ensembl:ENSG00000125744 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1221796527 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122159,RMVar_hsa_circ_105197,RMVar_hsa_circ_195356,RMVar_hsa_circ_195358,RMVar_hsa_circ_107055,RMVar_hsa_circ_195357 14718 RMVar_ID_14718 Human_SNP_ID_667217484 A-to-I Human chr19 - 45487241 45487238 45487242 CAGAAGTTCAAGACCAGCCTCGGCAACATAGTAAGACCCCCATCTCTACAAAAAGGTTAAAAACT CAGAAGTTCAAGACCAGCCTCGGCAACATAG____ACCCCCATCTCTACAAAAAGGTTAAAAACT TCTTA T RTN2 Ensembl:ENSG00000125744 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965985602 Functional Loss DEL dbSNP153 32..35 33 - - - RMVar_hsa_circ_122159,RMVar_hsa_circ_105197,RMVar_hsa_circ_195356,RMVar_hsa_circ_195358,RMVar_hsa_circ_107055,RMVar_hsa_circ_195357 14719 RMVar_ID_14719 Human_SNP_ID_667224799 A-to-I Human chr19 + 45510406 45510406 45510406 TGCCACCATGCCCGGCTAATTTTTATATTTTTAGTAGAGATAGGGTTTCACCGTGATGGCCAGGC TGCCACCATGCCCGGCTAATTTTTATATTTTTGGTAGAGATAGGGTTTCACCGTGATGGCCAGGC A G VASP Ensembl:ENSG00000125753 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1439725955 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110679,RMVar_hsa_circ_195364 14720 RMVar_ID_14720 Human_SNP_ID_667225166 A-to-I Human chr19 + 45511887 45511887 45511887 GGGAGGTCGAGGCAGGCAGATCACCTGAGGTCAGGAGTTTGAGGCCAGCCTGGCCAATGTGGCAA GGGAGGTCGAGGCAGGCAGATCACCTGAGGTCCGGAGTTTGAGGCCAGCCTGGCCAATGTGGCAA A C VASP Ensembl:ENSG00000125753 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1268074208 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110679,RMVar_hsa_circ_195364 14721 RMVar_ID_14721 Human_SNP_ID_667225179 A-to-I Human chr19 + 45511983 45511983 45511983 AACATTAGCCTGGCGTGGTGGCACACGTTTGTAATCCCGGACACTCAGAAGGCTGAGGCAGGAGA AACATTAGCCTGGCGTGGTGGCACACGTTTGTGATCCCGGACACTCAGAAGGCTGAGGCAGGAGA A G VASP Ensembl:ENSG00000125753 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs951295372 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110679,RMVar_hsa_circ_195364 14722 RMVar_ID_14722 Human_SNP_ID_667227111 A-to-I Human chr19 + 45518790 45518790 45518790 GGGCTCAAGTGATCCTCTTGCCTCAGCCTCCTAAGTAGCTGGGAATACAGGTGTGCACCACCATA GGGCTCAAGTGATCCTCTTGCCTCAGCCTCCTGAGTAGCTGGGAATACAGGTGTGCACCACCATA A G VASP Ensembl:ENSG00000125753 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1055489877 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23226,RMVar_hsa_circ_37509,RMVar_hsa_circ_110679,RMVar_hsa_circ_358294,RMVar_hsa_circ_195364,RMVar_hsa_circ_59314 14723 RMVar_ID_14723 Human_SNP_ID_667230782 A-to-I Human chr19 + 45530260 45530260 45530260 CCTCTAATACCAGCTACTCTGGAAGTTGAAGCAGGAGAATCGCTTGAAACAGGGAGGCAGAGGCT CCTCTAATACCAGCTACTCTGGAAGTTGAAGCCGGAGAATCGCTTGAAACAGGGAGGCAGAGGCT A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1168388005 Functional Loss SNV dbSNP153 33..33 33 - - - 14724 RMVar_ID_14724 Human_SNP_ID_667230784 A-to-I Human chr19 + 45530274 45530274 45530274 TACTCTGGAAGTTGAAGCAGGAGAATCGCTTGAAACAGGGAGGCAGAGGCTGCAGTGAGCCGAGA TACTCTGGAAGTTGAAGCAGGAGAATCGCTTGTAACAGGGAGGCAGAGGCTGCAGTGAGCCGAGA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs916508855 Functional Loss SNV dbSNP153 33..33 33 - - - 14725 RMVar_ID_14725 Human_SNP_ID_667235992 A-to-I Human chr19 - 45549681 45549681 45549681 GATGTTAGGAGATCGAGACCAGCCTGGCCAACATGGCAAAACCCCGTCTCTACTAAAAATACAAA GATGTTAGGAGATCGAGACCAGCCTGGCCAACGTGGCAAAACCCCGTCTCTACTAAAAATACAAA T C OPA3 Ensembl:ENSG00000125741 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1418842378 Functional Loss SNV dbSNP153 33..33 33 - - - 14726 RMVar_ID_14726 Human_SNP_ID_667236040 A-to-I Human chr19 - 45549914 45549914 45549914 ACCTCAGGTAATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGC ACCTCAGGTAATCCGCCCGCCTCGGCCTCCCAGAGTGCTGGGATTACAGGCGTGAGCCACCGCGC T C OPA3 Ensembl:ENSG00000125741 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1194444861 Functional Loss SNV dbSNP153 33..33 33 - - - 14727 RMVar_ID_14727 Human_SNP_ID_667236051 A-to-I Human chr19 - 45549937 45549937 45549937 CCCAGGCTGATCTTGAACTCCTGACCTCAGGTAATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGG CCCAGGCTGATCTTGAACTCCTGACCTCAGGTTATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGG T A OPA3 Ensembl:ENSG00000125741 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,31158229,31158229,31158229 RNA-Seq:(High) rs946136123 Functional Loss SNV dbSNP153 33..33 33 - - - 14728 RMVar_ID_14728 Human_SNP_ID_667236052 A-to-I Human chr19 - 45549937 45549937 45549937 CCCAGGCTGATCTTGAACTCCTGACCTCAGGTAATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGG CCCAGGCTGATCTTGAACTCCTGACCTCAGGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGG T C OPA3 Ensembl:ENSG00000125741 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,31158229,31158229,31158229 RNA-Seq:(High) rs946136123 Functional Loss SNV dbSNP153 33..33 33 - - - 14729 RMVar_ID_14729 Human_SNP_ID_667236061 A-to-I Human chr19 - 45549974 45549974 45549974 TTTTGTATTTTAGTGGAGACGGGGTTTCTCCAAGTTGCCCAGGCTGATCTTGAACTCCTGACCTC TTTTGTATTTTAGTGGAGACGGGGTTTCTCCAGGTTGCCCAGGCTGATCTTGAACTCCTGACCTC T C OPA3 Ensembl:ENSG00000125741 Protein coding intron GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,29796672,31158229,31158229,31158229,32596459,32596459 RNA-Seq:(High) rs1287347316 Functional Loss SNV dbSNP153 33..33 33 - - - 14730 RMVar_ID_14730 Human_SNP_ID_667236080 A-to-I Human chr19 - 45550071 45550071 45550071 TCACTGCAACTTCTACCTCCCAGGCTCAACCAATGATCCTGCCTCAGCTTCCGAAGTAGCTGGGA TCACTGCAACTTCTACCTCCCAGGCTCAACCAGTGATCCTGCCTCAGCTTCCGAAGTAGCTGGGA T C OPA3 Ensembl:ENSG00000125741 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs768641413 Functional Loss SNV dbSNP153 33..33 33 - - - 14731 RMVar_ID_14731 Human_SNP_ID_667236083 A-to-I Human chr19 - 45550082 45550082 45550082 GCAATCTCGGCTCACTGCAACTTCTACCTCCCAGGCTCAACCAATGATCCTGCCTCAGCTTCCGA GCAATCTCGGCTCACTGCAACTTCTACCTCCCGGGCTCAACCAATGATCCTGCCTCAGCTTCCGA T C OPA3 Ensembl:ENSG00000125741 Protein coding intron GSE38233;GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;ASD brains,temporal_cortex;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,30559470,31158229,31158229,32596459 RNA-Seq:(High) rs1408099284 Functional Loss SNV dbSNP153 33..33 33 - - - 14732 RMVar_ID_14732 Human_SNP_ID_667236089 A-to-I Human chr19 - 45550101 45550101 45550101 CCTGACGGAGTGCAGTGGTGCAATCTCGGCTCACTGCAACTTCTACCTCCCAGGCTCAACCAATG CCTGACGGAGTGCAGTGGTGCAATCTCGGCTCCCTGCAACTTCTACCTCCCAGGCTCAACCAATG T G OPA3 Ensembl:ENSG00000125741 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs1304778119 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_867167 14733 RMVar_ID_14733 Human_SNP_ID_667236093 A-to-I Human chr19 - 45550111 45550111 45550111 GCTCCGTCACCCTGACGGAGTGCAGTGGTGCAATCTCGGCTCACTGCAACTTCTACCTCCCAGGC GCTCCGTCACCCTGACGGAGTGCAGTGGTGCAGTCTCGGCTCACTGCAACTTCTACCTCCCAGGC T C OPA3 Ensembl:ENSG00000125741 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1467584760 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26474105 14734 RMVar_ID_14734 Human_SNP_ID_667236094 A-to-I Human chr19 - 45550120 45550120 45550120 GACAGTCTAGCTCCGTCACCCTGACGGAGTGCAGTGGTGCAATCTCGGCTCACTGCAACTTCTAC GACAGTCTAGCTCCGTCACCCTGACGGAGTGCGGTGGTGCAATCTCGGCTCACTGCAACTTCTAC T C OPA3 Ensembl:ENSG00000125741 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs561119752 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26474105 14735 RMVar_ID_14735 Human_SNP_ID_667236308 A-to-I Human chr19 - 45551015 45551015 45551015 TCGAGGCTGCAGCGAGCCGTGATCGCGCCACTACACTCCAGCCTGGATGACAGAGTGAGACCCTT TCGAGGCTGCAGCGAGCCGTGATCGCGCCACTGCACTCCAGCCTGGATGACAGAGTGAGACCCTT T C OPA3 Ensembl:ENSG00000125741 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1302779924 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_95748,Human_miRNA_ID_291959,Human_miRNA_ID_1770866 14736 RMVar_ID_14736 Human_SNP_ID_667236372 A-to-I Human chr19 - 45551245 45551245 45551245 GAGTACGCTGGCGTCCAGGTGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGACCAGGGC GAGTACGCTGGCGTCCAGGTGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGACCAGGGC T C OPA3 Ensembl:ENSG00000125741 Protein coding intron GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 ASD brains,temporal_cortex;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 30559470,31158229,31158229,31158229 RNA-Seq:(High) rs1460478301 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_773787 Human_miRNA_ID_1685703,Human_miRNA_ID_1738646 14737 RMVar_ID_14737 Human_SNP_ID_667236805 A-to-I Human chr19 - 45552957 45552957 45552957 GAAAAAAACGGTGCGGCTGGGAGCGGTGGCTCACGCCTGTAATCCTAGCACCTTGGGAGGCCGAG GAAAAAAACGGTGCGGCTGGGAGCGGTGGCTCTCGCCTGTAATCCTAGCACCTTGGGAGGCCGAG T A OPA3 Ensembl:ENSG00000125741 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1435875577 Functional Loss SNV dbSNP153 33..33 33 - - - 14738 RMVar_ID_14738 Human_SNP_ID_667239468 A-to-I Human chr19 - 45562637 45562615 45562637 GTGTCTCCCAGGCTGGGCAGTGGCGCGATCTCAGCTCACTGCAACCTCTGCCTCCCAGGTTCAAG GTGTCTCCCAGGCTGGGCAGTGGCGCGATCTC______________________CCAGGTTCAAG GGAGGCAGAGGTTGCAGTGAGCT G OPA3 Ensembl:ENSG00000125741 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1304751103 Functional Loss DEL dbSNP153 33..54 33 - - - 14739 RMVar_ID_14739 Human_SNP_ID_667240907 A-to-I Human chr19 - 45568075 45568075 45568075 AGAATCACTTGACCTTTGGAGGCTCAGGTTGTAGTGAGCTGAGATCGTACCAGTGCACTCCAGCT AGAATCACTTGACCTTTGGAGGCTCAGGTTGTGGTGAGCTGAGATCGTACCAGTGCACTCCAGCT T C OPA3 Ensembl:ENSG00000125741 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1213342046 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13475568 14740 RMVar_ID_14740 Human_SNP_ID_667241787 A-to-I Human chr19 - 45571348 45571348 45571348 GAGGCGGGGAGTTCAAGACCAACCTGAACAACATGGAGAAACCCCGTCTCTACTAAAAAAATACA GAGGCGGGGAGTTCAAGACCAACCTGAACAACGTGGAGAAACCCCGTCTCTACTAAAAAAATACA T C OPA3 Ensembl:ENSG00000125741 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1332784452 Functional Loss SNV dbSNP153 33..33 33 - - - 14741 RMVar_ID_14741 Human_SNP_ID_667253238 A-to-I Human chr19 - 45610275 45610275 45610275 CTCCTGCCTCAGCCTCCGAAGTAGCTCGGATTACGGGCATGCGCCACCACACCCAGCTAATTTTT CTCCTGCCTCAGCCTCCGAAGTAGCTCGGATTGCGGGCATGCGCCACCACACCCAGCTAATTTTT T C EML2 Ensembl:ENSG00000125746 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1225988605 Functional Loss SNV dbSNP153 33..33 33 - - - 14742 RMVar_ID_14742 Human_SNP_ID_667253249 A-to-I Human chr19 - 45610314 45610314 45610314 TGGCTCACTGCAACCTCCGACTCCCTGGTTCAAGTGATTCTCCTGCCTCAGCCTCCGAAGTAGCT TGGCTCACTGCAACCTCCGACTCCCTGGTTCAGGTGATTCTCCTGCCTCAGCCTCCGAAGTAGCT T C EML2 Ensembl:ENSG00000125746 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1273986502 Functional Loss SNV dbSNP153 33..33 33 - - - 14743 RMVar_ID_14743 Human_SNP_ID_667253345 A-to-I Human chr19 - 45610672 45610672 45610672 CCACGCCCGGCTAATTTTTTTGTATTTTTAGTAGAGACAGGGTTTTACCACGTTGGCCAGGCTGG CCACGCCCGGCTAATTTTTTTGTATTTTTAGTGGAGACAGGGTTTTACCACGTTGGCCAGGCTGG T C EML2 Ensembl:ENSG00000125746 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1438403880 Functional Loss SNV dbSNP153 33..33 33 - - - 14744 RMVar_ID_14744 Human_SNP_ID_667253846 A-to-I Human chr19 - 45612684 45612678 45612685 TCTTTCTCCTTTCTCTTCTTTTTTTATTTTTTATTTTTGAGACAGGGTCTCACTCTGTTGCCCAC TCTTTCTCCTTTCTCTTCTTTTTTTATTTTT_______GAGACAGGGTCTCACTCTGTTGCCCAC CAAAAATA C EML2 Ensembl:ENSG00000125746 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1014307317 Functional Loss DEL dbSNP153 32..38 33 - - - 14745 RMVar_ID_14745 Human_SNP_ID_667253847 A-to-I Human chr19 - 45612684 45612684 45612684 TCTTTCTCCTTTCTCTTCTTTTTTTATTTTTTATTTTTGAGACAGGGTCTCACTCTGTTGCCCAC TCTTTCTCCTTTCTCTTCTTTTTTTATTTTTTTTTTTTGAGACAGGGTCTCACTCTGTTGCCCAC T A EML2 Ensembl:ENSG00000125746 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1487195204 Functional Loss SNV dbSNP153 33..33 33 - - - 14746 RMVar_ID_14746 Human_SNP_ID_667255909 A-to-I Human chr19 - 45619820 45619820 45619820 TCTCGGACTCCTGAGCTCAATCTTCCTGCCTCAGCCTCCCAAAGTGTCGGGATTACCGGCGTGAG TCTCGGACTCCTGAGCTCAATCTTCCTGCCTCCGCCTCCCAAAGTGTCGGGATTACCGGCGTGAG T G EML2 Ensembl:ENSG00000125746 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1051139203 Functional Loss SNV dbSNP153 33..33 33 - - - 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_195382 14747 RMVar_ID_14747 Human_SNP_ID_667256017 A-to-I Human chr19 - 45620237 45620237 45620237 TGGTGGCGTGTGCCTGTAATCCCAGTTACTCAAAAGGCTGAGGCAGGAGAATTGCTTGAACCTGG TGGTGGCGTGTGCCTGTAATCCCAGTTACTCAGAAGGCTGAGGCAGGAGAATTGCTTGAACCTGG T C EML2 Ensembl:ENSG00000125746 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1056080134 Functional Loss SNV dbSNP153 33..33 33 - - - 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_195382 14748 RMVar_ID_14748 Human_SNP_ID_667256022 A-to-I Human chr19 - 45620270 45620270 45620270 TCTGTACTAAAAATACAAAACATTAGCTGGGCATGGTGGCGTGTGCCTGTAATCCCAGTTACTCA TCTGTACTAAAAATACAAAACATTAGCTGGGCGTGGTGGCGTGTGCCTGTAATCCCAGTTACTCA T C EML2 Ensembl:ENSG00000125746 Protein coding intron GSE123020:GSM3490829,GSM3490830,GSM3490831 esophageal squamous carcinoma cells,EC109 cell line - 32596459 RNA-Seq:(High) rs1001341523 Functional Loss SNV dbSNP153 33..33 33 - - - 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_195382 14749 RMVar_ID_14749 Human_SNP_ID_667256083 A-to-I Human chr19 - 45620626 45620626 45620626 TCGGCTCATTGCAAACTCTGCCTCCCGCTTCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCT TCGGCTCATTGCAAACTCTGCCTCCCGCTTCAGGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCT T C EML2 Ensembl:ENSG00000125746 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs896500631 Functional Loss SNV dbSNP153 33..33 33 - - - 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_195382 14750 RMVar_ID_14750 Human_SNP_ID_667256090 A-to-I Human chr19 - 45620661 45620661 45620661 CTCTGTTGCCCAGGCTGCAGCGCAGTGGCTCAATCTCGGCTCATTGCAAACTCTGCCTCCCGCTT CTCTGTTGCCCAGGCTGCAGCGCAGTGGCTCAGTCTCGGCTCATTGCAAACTCTGCCTCCCGCTT T C EML2 Ensembl:ENSG00000125746 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1464160886 Functional Loss SNV dbSNP153 33..33 33 - - - 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_195382 14751 RMVar_ID_14751 Human_SNP_ID_667256148 A-to-I Human chr19 - 45620865 45620865 45620865 ACCTCTCAGACTCCAGCTCCACGGATTGGGGAAGGTCCTGCTGGAGTCTGCTTGCATTTCTTCTC ACCTCTCAGACTCCAGCTCCACGGATTGGGGAGGGTCCTGCTGGAGTCTGCTTGCATTTCTTCTC T C EML2 Ensembl:ENSG00000125746 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1529723 Functional Loss SNV dbSNP153 33..33 33 - - - 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_79035,RMVar_hsa_circ_115644,RMVar_hsa_circ_195382,RMVar_hsa_circ_195383,RMVar_hsa_circ_195384 14752 RMVar_ID_14752 Human_SNP_ID_667256674 A-to-I Human chr19 - 45622466 45622466 45622466 AGATCATACCACTGCACTCCAGCCTGGTCGACAGAGCAAGACTTTGTCTCAAAAACAAAATAAAA AGATCATACCACTGCACTCCAGCCTGGTCGACGGAGCAAGACTTTGTCTCAAAAACAAAATAAAA T C EML2 Ensembl:ENSG00000125746 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1568452735 Functional Loss SNV dbSNP153 33..33 33 - - - 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_195387 14753 RMVar_ID_14753 Human_SNP_ID_667258827 A-to-I Human chr19 - 45630215 45630215 45630215 TTTGTTTTGTTTAAGAGACAGGGTCTCCCTATATTGCCTATGCTGGCCTCAAACTCCTGGACTCA TTTGTTTTGTTTAAGAGACAGGGTCTCCCTATGTTGCCTATGCTGGCCTCAAACTCCTGGACTCA T C EML2 Ensembl:ENSG00000125746 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1219232780 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2536,RMVar_hsa_circ_372977,RMVar_hsa_circ_195375,RMVar_hsa_circ_195378,RMVar_hsa_circ_108059,RMVar_hsa_circ_374975,RMVar_hsa_circ_195379,RMVar_hsa_circ_79035,RMVar_hsa_circ_115644,RMVar_hsa_circ_195383,RMVar_hsa_circ_195384,RMVar_hsa_circ_17504,RMVar_hsa_circ_92251,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_195395,RMVar_hsa_circ_39128,RMVar_hsa_circ_195394,RMVar_hsa_circ_195392,RMVar_hsa_circ_195390 14754 RMVar_ID_14754 Human_SNP_ID_667260738 A-to-I Human chr19 - 45636916 45636916 45636916 AGATATTTTCTTGTTTTTGAGACACCCAGGCTAGAGTGCAGTGGCACGATCTTGGCTCACTGCAA AGATATTTTCTTGTTTTTGAGACACCCAGGCTGGAGTGCAGTGGCACGATCTTGGCTCACTGCAA T C EML2 Ensembl:ENSG00000125746 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270400127 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_372977,RMVar_hsa_circ_195375,RMVar_hsa_circ_374975,RMVar_hsa_circ_195379,RMVar_hsa_circ_79035,RMVar_hsa_circ_195384,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_118469,RMVar_hsa_circ_195390,RMVar_hsa_circ_195400,RMVar_hsa_circ_96749,RMVar_hsa_circ_195401,RMVar_hsa_circ_195399 14755 RMVar_ID_14755 Human_SNP_ID_667261942 A-to-I Human chr19 - 45640620 45640620 45640620 AAGGTCAAGAGATCGAGACCATCCTGGCCAACATGGTGAAACCCCCTGTCTATTAATAATACAAA AAGGTCAAGAGATCGAGACCATCCTGGCCAACGTGGTGAAACCCCCTGTCTATTAATAATACAAA T C EML2 Ensembl:ENSG00000125746 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1484333824 Functional Loss SNV dbSNP153 33..33 33 - - - 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 14756 RMVar_ID_14756 Human_SNP_ID_667270606 A-to-I Human chr19 + 45670130 45670130 45670130 TCGGCTCACTACAACCTCCGTCTCCCGGGTTCAAGCGATTCTCCCGCCTCAGCCTCTCGAGTAGC TCGGCTCACTACAACCTCCGTCTCCCGGGTTCCAGCGATTCTCCCGCCTCAGCCTCTCGAGTAGC A C GIPR Ensembl:ENSG00000010310 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs987170894 Functional Loss SNV dbSNP153 33..33 33 - - - 14757 RMVar_ID_14757 Human_SNP_ID_667270611 A-to-I Human chr19 + 45670148 45670148 45670148 CGTCTCCCGGGTTCAAGCGATTCTCCCGCCTCAGCCTCTCGAGTAGCTGGGACTACAGGCGCACT CGTCTCCCGGGTTCAAGCGATTCTCCCGCCTCGGCCTCTCGAGTAGCTGGGACTACAGGCGCACT A G GIPR Ensembl:ENSG00000010310 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs567751290 Functional Loss SNV dbSNP153 33..33 33 - - - 14758 RMVar_ID_14758 Human_SNP_ID_667276390 A-to-I Human chr19 - 45689425 45689425 45689425 CACATCAAGTGATCAATCCACCTTGACCTCCTAAAGTGCTAGGATTACAGGCATGAGCCACTGTA CACATCAAGTGATCAATCCACCTTGACCTCCTGAAGTGCTAGGATTACAGGCATGAGCCACTGTA T C SNRPD2 Ensembl:ENSG00000125743 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1474506374 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113835,RMVar_hsa_circ_195410 14759 RMVar_ID_14759 Human_SNP_ID_667276738 A-to-I Human chr19 - 45690444 45690443 45690444 GTCTCGCTCTGTCACCCAGATTGGAGTGTAGTAGCACGAGCTCTGTCTCCTGGGTTCAAGCGATC GTCTCGCTCTGTCACCCAGATTGGAGTGTAGT_GCACGAGCTCTGTCTCCTGGGTTCAAGCGATC CT C SNRPD2 Ensembl:ENSG00000125743 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs796656531 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_113835,RMVar_hsa_circ_195410 14760 RMVar_ID_14760 Human_SNP_ID_667276751 A-to-I Human chr19 - 45690483 45690483 45690483 ATGGGAGGGTTTTCTTTTGTTTTGTTTGTTTGAGATGGAGTCTCGCTCTGTCACCCAGATTGGAG ATGGGAGGGTTTTCTTTTGTTTTGTTTGTTTGGGATGGAGTCTCGCTCTGTCACCCAGATTGGAG T C SNRPD2 Ensembl:ENSG00000125743 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1214643829 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6773729 RMVar_hsa_circ_113835,RMVar_hsa_circ_195410 14761 RMVar_ID_14761 Human_SNP_ID_667276975 A-to-I Human chr19 - 45691263 45691263 45691263 AGCCGGCCGTAGTGGCGGGCGCCTGTAATTGCAGCTATTCGGGAGGCTGAGGCCGGAGGATCGCT AGCCGGCCGTAGTGGCGGGCGCCTGTAATTGCGGCTATTCGGGAGGCTGAGGCCGGAGGATCGCT T C SNRPD2 Ensembl:ENSG00000125743 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1419732997 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113835,RMVar_hsa_circ_195410 14762 RMVar_ID_14762 Human_SNP_ID_667277016 A-to-I Human chr19 - 45691413 45691413 45691413 CGAATACTGGGGGAGGCCGAGCGCGGTGGCTCAGGTTTGTAAATCCCAGCACTTTGGGAGGCCGA CGAATACTGGGGGAGGCCGAGCGCGGTGGCTCGGGTTTGTAAATCCCAGCACTTTGGGAGGCCGA T C SNRPD2 Ensembl:ENSG00000125743 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1287831066 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6773736,Human_RBP_ID_13475733 Human_Splice_Rec_2020527 RMVar_hsa_circ_113835,RMVar_hsa_circ_195410 14763 RMVar_ID_14763 Human_SNP_ID_667277862 A-to-I Human chr19 + 45693897 45693897 45693897 CAGATAATAAGTAGTAGACCTTAGCCGGGTGCAGTGGCTCATGCCTGTAATCCCAGCACTTTGGG CAGATAATAAGTAGTAGACCTTAGCCGGGTGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGG A G QPCTL Ensembl:ENSG00000011478 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs893672403 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5131358 14764 RMVar_ID_14764 Human_SNP_ID_667278028 A-to-I Human chr19 + 45694581 45694581 45694581 CAACCTCCACCTCCCAGGTTCAAGCAAATCTCATGCTTCAGCCTCCTGAGTAGCTGGGATTACAG CAACCTCCACCTCCCAGGTTCAAGCAAATCTCTTGCTTCAGCCTCCTGAGTAGCTGGGATTACAG A T QPCTL Ensembl:ENSG00000011478 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs982262941 Functional Loss SNV dbSNP153 33..33 33 - - - 14765 RMVar_ID_14765 Human_SNP_ID_667278033 A-to-I Human chr19 + 45694610 45694602 45694610 CTCATGCTTCAGCCTCCTGAGTAGCTGGGATTACAGGTGTGCACCACCATGCCTGGCTAATTTTT CTCATGCTTCAGCCTCCTGAGTAGC________CAGGTGTGCACCACCATGCCTGGCTAATTTTT CTGGGATTA C QPCTL Ensembl:ENSG00000011478 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs547546913 Functional Loss DEL dbSNP153 26..33 33 - - - 14766 RMVar_ID_14766 Human_SNP_ID_667278052 A-to-I Human chr19 + 45694673 45694673 45694673 TTTGTATTTTTAGTGAGACGGGGTTTCACCATATTGGCCAGGCTGGTCTCAAACTCCTGACCTTA TTTGTATTTTTAGTGAGACGGGGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTCCTGACCTTA A G QPCTL Ensembl:ENSG00000011478 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1318106080 Functional Loss SNV dbSNP153 33..33 33 - - - 14767 RMVar_ID_14767 Human_SNP_ID_667278067 A-to-I Human chr19 + 45694730 45694730 45694730 TGACCTTATGATCCGCCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGC TGACCTTATGATCCGCCCACCTCAGCCTCCCAGAGTGCTGGGATTACAGGCGTGAGCCACCGCGC A G QPCTL Ensembl:ENSG00000011478 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs551951645 Functional Loss SNV dbSNP153 33..33 33 - - - 14768 RMVar_ID_14768 Human_SNP_ID_667279455 A-to-I Human chr19 + 45699437 45699437 45699437 TAGAGCCTGGGAGGTCAAGGCTATAGTGAGCCAAGATTGCGCCACTGCACTCCAGCCTGGGCAAC TAGAGCCTGGGAGGTCAAGGCTATAGTGAGCCCAGATTGCGCCACTGCACTCCAGCCTGGGCAAC A C QPCTL Ensembl:ENSG00000011478 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs562191423 Functional Loss SNV dbSNP153 33..33 33 - - - 14769 RMVar_ID_14769 Human_SNP_ID_667279996 A-to-I Human chr19 + 45701181 45701181 45701181 GGGGCATGCGCCTGAAGTCCTAGCTATTTGGGAGGCTGAGACTGAAGGATCACTTAGGCCAGCGA GGGGCATGCGCCTGAAGTCCTAGCTATTTGGGGGGCTGAGACTGAAGGATCACTTAGGCCAGCGA A G QPCTL Ensembl:ENSG00000011478 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1022098016 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17568688 14770 RMVar_ID_14770 Human_SNP_ID_667280759 A-to-I Human chr19 + 45703743 45703743 45703743 GAGAGGCTGAGGGGGAAGGATCACCCGAGGTCAGGAGTTTGAGACCAGCCTGGTCAACATGGCGA GAGAGGCTGAGGGGGAAGGATCACCCGAGGTCGGGAGTTTGAGACCAGCCTGGTCAACATGGCGA A G QPCTL Ensembl:ENSG00000011478 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1302752963 Functional Loss SNV dbSNP153 33..33 33 - - - 14771 RMVar_ID_14771 Human_SNP_ID_667280780 A-to-I Human chr19 + 45703868 45703868 45703868 TCAGCTGCTTGGGAGGCTGAGGCAGGAGAATCACTTGTACGCAGGAGGCGGAGGTTGCAGTGAGC TCAGCTGCTTGGGAGGCTGAGGCAGGAGAATCGCTTGTACGCAGGAGGCGGAGGTTGCAGTGAGC A G QPCTL Ensembl:ENSG00000011478 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1468798519 Functional Loss SNV dbSNP153 33..33 33 - - - 14772 RMVar_ID_14772 Human_SNP_ID_667285863 A-to-I Human chr19 - 45721250 45721250 45721250 ACCCTCCACTTCCGGGCTCAAGCGATCCTCCCACTTCAGCCTCCCGAGTAGCTGTGACTGCAGGC ACCCTCCACTTCCGGGCTCAAGCGATCCTCCCGCTTCAGCCTCCCGAGTAGCTGTGACTGCAGGC T C FBXO46 Ensembl:ENSG00000177051 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1177509014 Functional Loss SNV dbSNP153 33..33 33 - - - 14773 RMVar_ID_14773 Human_SNP_ID_667286478 A-to-I Human chr19 - 45723745 45723745 45723745 TGAAGCAGAAGAATTGCTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCTGAGATCATGCCACTGC TGAAGCAGAAGAATTGCTTGAACCTGGGAGGCGGAGGTTGCAGTGAGCTGAGATCATGCCACTGC T C FBXO46 Ensembl:ENSG00000177051 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs762221281 Functional Loss SNV dbSNP153 33..33 33 - - - 14774 RMVar_ID_14774 Human_SNP_ID_667286505 A-to-I Human chr19 - 45723824 45723824 45723824 GAAACCCTGTCTCTACTAAAAATACAAAAATTAGCTGGGCGTGGTGGCGCACGCCTGTAGTCCCA GAAACCCTGTCTCTACTAAAAATACAAAAATTGGCTGGGCGTGGTGGCGCACGCCTGTAGTCCCA T C FBXO46 Ensembl:ENSG00000177051 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1167351734 Functional Loss SNV dbSNP153 33..33 33 - - - 14775 RMVar_ID_14775 Human_SNP_ID_667286674 A-to-I Human chr19 - 45724635 45724635 45724635 GAAAAAATAAGAAATTTTTTTTTTGTAGAGACAGGGTCTTGCTATATTGCCCAGGCTGCTCTCAA GAAAAAATAAGAAATTTTTTTTTTGTAGAGACGGGGTCTTGCTATATTGCCCAGGCTGCTCTCAA T C FBXO46 Ensembl:ENSG00000177051 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs943364729 Functional Loss SNV dbSNP153 33..33 33 - - - 14776 RMVar_ID_14776 Human_SNP_ID_667286931 A-to-I Human chr19 - 45725715 45725715 45725715 TTATTTAAGTTTTTGAGACAAAGTCTGGCTCTATTGCCCAGGTTGGAGTGCAGTGGTACAGTCTC TTATTTAAGTTTTTGAGACAAAGTCTGGCTCTGTTGCCCAGGTTGGAGTGCAGTGGTACAGTCTC T C FBXO46 Ensembl:ENSG00000177051 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1404051086 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13476088 14777 RMVar_ID_14777 Human_SNP_ID_667286986 A-to-I Human chr19 - 45725964 45725964 45725964 TGGAGGTTGAGGCGGGAGGATCACTTGGGCCCAGGAGGTGGAAGGTGCAGTGAGCTCTGATTGCC TGGAGGTTGAGGCGGGAGGATCACTTGGGCCCGGGAGGTGGAAGGTGCAGTGAGCTCTGATTGCC T C FBXO46 Ensembl:ENSG00000177051 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs533015784 Functional Loss SNV dbSNP153 33..33 33 - - - 14778 RMVar_ID_14778 Human_SNP_ID_667286988 A-to-I Human chr19 - 45725974 45725974 45725974 CCAGCACCTCTGGAGGTTGAGGCGGGAGGATCACTTGGGCCCAGGAGGTGGAAGGTGCAGTGAGC CCAGCACCTCTGGAGGTTGAGGCGGGAGGATCGCTTGGGCCCAGGAGGTGGAAGGTGCAGTGAGC T C FBXO46 Ensembl:ENSG00000177051 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1568549581 Functional Loss SNV dbSNP153 33..33 33 - - - 14779 RMVar_ID_14779 Human_SNP_ID_667286994 A-to-I Human chr19 - 45726020 45726020 45726020 AATTTTTTAAAAAATTAGTCAGGCTTGGTGGCATGAGCCTATAGTCCCAGCACCTCTGGAGGTTG AATTTTTTAAAAAATTAGTCAGGCTTGGTGGCTTGAGCCTATAGTCCCAGCACCTCTGGAGGTTG T A FBXO46 Ensembl:ENSG00000177051 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs548853716 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13476094 14780 RMVar_ID_14780 Human_SNP_ID_667287000 A-to-I Human chr19 - 45726044 45726044 45726044 AGCCACTGCACCCAGCCTCAAATAAATTTTTTAAAAAATTAGTCAGGCTTGGTGGCATGAGCCTA AGCCACTGCACCCAGCCTCAAATAAATTTTTTTAAAAATTAGTCAGGCTTGGTGGCATGAGCCTA T A FBXO46 Ensembl:ENSG00000177051 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs182327913 Functional Loss SNV dbSNP153 33..33 33 - - - 14781 RMVar_ID_14781 Human_SNP_ID_667287001 A-to-I Human chr19 - 45726044 45726044 45726044 AGCCACTGCACCCAGCCTCAAATAAATTTTTTAAAAAATTAGTCAGGCTTGGTGGCATGAGCCTA AGCCACTGCACCCAGCCTCAAATAAATTTTTTGAAAAATTAGTCAGGCTTGGTGGCATGAGCCTA T C FBXO46 Ensembl:ENSG00000177051 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs182327913 Functional Loss SNV dbSNP153 33..33 33 - - - 14782 RMVar_ID_14782 Human_SNP_ID_667287085 A-to-I Human chr19 - 45726397 45726397 45726397 GTGATCCACCCGCCTCAACCTTCCAAAGTGCTAGAATTACAGGTGTGAGCCACCGTGCCCAGCCA GTGATCCACCCGCCTCAACCTTCCAAAGTGCTGGAATTACAGGTGTGAGCCACCGTGCCCAGCCA T C FBXO46 Ensembl:ENSG00000177051 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1024877442 Functional Loss SNV dbSNP153 33..33 33 - - - 14783 RMVar_ID_14783 Human_SNP_ID_667287086 A-to-I Human chr19 - 45726397 45726397 45726397 GTGATCCACCCGCCTCAACCTTCCAAAGTGCTAGAATTACAGGTGTGAGCCACCGTGCCCAGCCA GTGATCCACCCGCCTCAACCTTCCAAAGTGCTCGAATTACAGGTGTGAGCCACCGTGCCCAGCCA T G FBXO46 Ensembl:ENSG00000177051 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1024877442 Functional Loss SNV dbSNP153 33..33 33 - - - 14784 RMVar_ID_14784 Human_SNP_ID_667287107 A-to-I Human chr19 - 45726482 45726480 45726483 CTCTATGCCCTGCTAATTTTTATATTTTTAGTAGAGACGAGATTTCGTTGTGTTGGCCAGGATGG CTCTATGCCCTGCTAATTTTTATATTTTTAG___AGACGAGATTTCGTTGTGTTGGCCAGGATGG TCTA T FBXO46 Ensembl:ENSG00000177051 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1340586638 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_13476100 14785 RMVar_ID_14785 Human_SNP_ID_667287341 A-to-I Human chr19 - 45727475 45727474 45727475 GGCTCACTGCAATCTCCGCCTCCCGGGTTCAAATGATGTCTTCTGCCTCAGCCTCCTGCGTAGCT GGCTCACTGCAATCTCCGCCTCCCGGGTTCAA_TGATGTCTTCTGCCTCAGCCTCCTGCGTAGCT AT A FBXO46 Ensembl:ENSG00000177051 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs989376274 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_6773890 14786 RMVar_ID_14786 Human_SNP_ID_667287342 A-to-I Human chr19 - 45727475 45727475 45727475 GGCTCACTGCAATCTCCGCCTCCCGGGTTCAAATGATGTCTTCTGCCTCAGCCTCCTGCGTAGCT GGCTCACTGCAATCTCCGCCTCCCGGGTTCAAGTGATGTCTTCTGCCTCAGCCTCCTGCGTAGCT T C FBXO46 Ensembl:ENSG00000177051 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs916503983 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6773890 14787 RMVar_ID_14787 Human_SNP_ID_667287623 A-to-I Human chr19 - 45728656 45728656 45728656 TTTATTTTTATTTTTGTAGAGACGCGGGTCTTACTTTGTTGCCCAGGCTGGTCTCAAATTCCTAG TTTATTTTTATTTTTGTAGAGACGCGGGTCTTTCTTTGTTGCCCAGGCTGGTCTCAAATTCCTAG T A FBXO46 Ensembl:ENSG00000177051 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1568550200 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_140704 14788 RMVar_ID_14788 Human_SNP_ID_667287808 A-to-I Human chr19 - 45729348 45729348 45729348 TGGCTAACTGTAGCCTCTGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGTT TGGCTAACTGTAGCCTCTGCCTCCCGGGTTCAGGCGATTCTCCTGCCTCAGCCTCCTGAGTAGTT T C FBXO46 Ensembl:ENSG00000177051 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1047647048 Functional Loss SNV dbSNP153 33..33 33 - - - 14789 RMVar_ID_14789 Human_SNP_ID_667287823 A-to-I Human chr19 - 45729417 45729417 45729417 TTTTATTTATTTTTATTTATTTATTTAGAGACAGTCTCCCTCTGTCACCCAGGCTGGAGTGCAGT TTTTATTTATTTTTATTTATTTATTTAGAGACGGTCTCCCTCTGTCACCCAGGCTGGAGTGCAGT T C FBXO46 Ensembl:ENSG00000177051 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1464549109 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6805412,Human_RBP_ID_13476165 14790 RMVar_ID_14790 Human_SNP_ID_667290537 A-to-I Human chr19 + 45740738 45740738 45740738 TGCCACTGTACTCCAGCCTGGGCAACAAGGCGAGACTCCATCTCAATAATAATAATAATAATAAT TGCCACTGTACTCCAGCCTGGGCAACAAGGCGGGACTCCATCTCAATAATAATAATAATAATAAT A G BHMG1 Ensembl:ENSG00000237452 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs999118513 Functional Loss SNV dbSNP153 33..33 33 - - - 14791 RMVar_ID_14791 Human_SNP_ID_667321819 A-to-I Human chr19 - 45836509 45836509 45836509 CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGTGCCTGCCACCACGCCCAGCTAAGTTTT CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTGCAGGTGCCTGCCACCACGCCCAGCTAAGTTTT T C SYMPK Ensembl:ENSG00000125755 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1156332262 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35442,RMVar_hsa_circ_77690,RMVar_hsa_circ_120935,RMVar_hsa_circ_195416,RMVar_hsa_circ_195419,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_378888,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_299463,RMVar_hsa_circ_195431,RMVar_hsa_circ_28038,RMVar_hsa_circ_45009,RMVar_hsa_circ_195432,RMVar_hsa_circ_195433 14792 RMVar_ID_14792 Human_SNP_ID_667323131 A-to-I Human chr19 - 45841187 45841187 45841187 CTGAGGTCAGGAGTTCGAAATTAGCCTGGCTAACATGGTGAAACCCTGTCTCTACTAAAAATACA CTGAGGTCAGGAGTTCGAAATTAGCCTGGCTAGCATGGTGAAACCCTGTCTCTACTAAAAATACA T C SYMPK Ensembl:ENSG00000125755 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs953295295 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77690,RMVar_hsa_circ_195419,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_28038,RMVar_hsa_circ_45009,RMVar_hsa_circ_195432,RMVar_hsa_circ_195433,RMVar_hsa_circ_195436,RMVar_hsa_circ_314742,RMVar_hsa_circ_335784,RMVar_hsa_circ_355438,RMVar_hsa_circ_301796,RMVar_hsa_circ_195435 14793 RMVar_ID_14793 Human_SNP_ID_667323145 A-to-I Human chr19 - 45841275 45841275 45841275 AAAAAAAAAAGGTGGGGGGGGAATTGCCAGGCACAGTGGCTCATGCCTGTAATCCCAGCATTTTG AAAAAAAAAAGGTGGGGGGGGAATTGCCAGGCGCAGTGGCTCATGCCTGTAATCCCAGCATTTTG T C SYMPK Ensembl:ENSG00000125755 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1343438116 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77690,RMVar_hsa_circ_195419,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_28038,RMVar_hsa_circ_45009,RMVar_hsa_circ_195432,RMVar_hsa_circ_195433,RMVar_hsa_circ_195436,RMVar_hsa_circ_314742,RMVar_hsa_circ_335784,RMVar_hsa_circ_355438,RMVar_hsa_circ_301796,RMVar_hsa_circ_195435 14794 RMVar_ID_14794 Human_SNP_ID_667323205 A-to-I Human chr19 - 45841430 45841430 45841430 AAATTAGCTGGGTGTAGTGGTGCATGCCTGTAATCCCAGATACTCTGGAGGCTGAGGCAGGAGAA AAATTAGCTGGGTGTAGTGGTGCATGCCTGTAGTCCCAGATACTCTGGAGGCTGAGGCAGGAGAA T C SYMPK Ensembl:ENSG00000125755 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1161181252 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77690,RMVar_hsa_circ_195419,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_28038,RMVar_hsa_circ_45009,RMVar_hsa_circ_195432,RMVar_hsa_circ_195433,RMVar_hsa_circ_195436,RMVar_hsa_circ_314742,RMVar_hsa_circ_335784,RMVar_hsa_circ_355438,RMVar_hsa_circ_301796,RMVar_hsa_circ_195435 14795 RMVar_ID_14795 Human_SNP_ID_667323999 A-to-I Human chr19 - 45844179 45844179 45844179 CTGTCTCTTAGACGTGCTATGGGAAGAGGGCAAGGCAGCCTTGGAGCAGCTGCTTAAGTTCATGG CTGTCTCTTAGACGTGCTATGGGAAGAGGGCAGGGCAGCCTTGGAGCAGCTGCTTAAGTTCATGG T C SYMPK Ensembl:ENSG00000125755 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs770608220 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 14796 RMVar_ID_14796 Human_SNP_ID_667324736 A-to-I Human chr19 - 45846967 45846967 45846967 CAACATGGTGAAACCCCTTATCTACTGAAAATACAAAAATTAGCCGGGCATGGTGGCGGGCACCT CAACATGGTGAAACCCCTTATCTACTGAAAATGCAAAAATTAGCCGGGCATGGTGGCGGGCACCT T C SYMPK Ensembl:ENSG00000125755 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1235311206 Functional Loss SNV dbSNP153 33..33 33 - - - 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 14797 RMVar_ID_14797 Human_SNP_ID_667327023 A-to-I Human chr19 - 45854975 45854975 45854975 TACTTGGGAGGCTGAGGCAGGAGAATCACTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCTGAGA TACTTGGGAGGCTGAGGCAGGAGAATCACTTGCACCTGGGAGGCAGAGGTTGCAGTGAGCTGAGA T G SYMPK Ensembl:ENSG00000125755 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1233634849 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92180,RMVar_hsa_circ_195447 14798 RMVar_ID_14798 Human_SNP_ID_667327028 A-to-I Human chr19 - 45854989 45854989 45854989 CCCGTAATCCCAGTTACTTGGGAGGCTGAGGCAGGAGAATCACTTGAACCTGGGAGGCAGAGGTT CCCGTAATCCCAGTTACTTGGGAGGCTGAGGCGGGAGAATCACTTGAACCTGGGAGGCAGAGGTT T C SYMPK Ensembl:ENSG00000125755 Protein coding intron GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs1455747995 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92180,RMVar_hsa_circ_195447 14799 RMVar_ID_14799 Human_SNP_ID_667327058 A-to-I Human chr19 - 45855117 45855117 45855117 TCCCTGCACTTTGGGAGGCCGAGGCAGGTGGAACACCTGAGGTCAGGAGTTTGACACCAGCCTGG TCCCTGCACTTTGGGAGGCCGAGGCAGGTGGATCACCTGAGGTCAGGAGTTTGACACCAGCCTGG T A SYMPK Ensembl:ENSG00000125755 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1568627115 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92180,RMVar_hsa_circ_195447 14800 RMVar_ID_14800 Human_SNP_ID_667327070 A-to-I Human chr19 - 45855151 45855151 45855151 ACTCTGGGCCAGGCACTGTGGTTCACGCCTGTAATCCCTGCACTTTGGGAGGCCGAGGCAGGTGG ACTCTGGGCCAGGCACTGTGGTTCACGCCTGTCATCCCTGCACTTTGGGAGGCCGAGGCAGGTGG T G SYMPK Ensembl:ENSG00000125755 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1341665276 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13477121 RMVar_hsa_circ_92180,RMVar_hsa_circ_195447 14801 RMVar_ID_14801 Human_SNP_ID_667327318 A-to-I Human chr19 - 45856143 45856143 45856143 CACCATGTTGGCCAGGCTGGTCTCAAACTCCTAACCTCAGACGATCCACCCGTTTCGGCCTCCCA CACCATGTTGGCCAGGCTGGTCTCAAACTCCTCACCTCAGACGATCCACCCGTTTCGGCCTCCCA T G SYMPK Ensembl:ENSG00000125755 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs999711549 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92180,RMVar_hsa_circ_195447 14802 RMVar_ID_14802 Human_SNP_ID_667327350 A-to-I Human chr19 - 45856283 45856283 45856283 CAGACTGGAGTGCAGTGGCATGATCTCGGCTCACTGCAACCTCCGCCTCCTGGGTTCAAGCGATT CAGACTGGAGTGCAGTGGCATGATCTCGGCTCGCTGCAACCTCCGCCTCCTGGGTTCAAGCGATT T C SYMPK Ensembl:ENSG00000125755 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs998370668 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92180,RMVar_hsa_circ_195447 14803 RMVar_ID_14803 Human_SNP_ID_667327466 A-to-I Human chr19 - 45856729 45856729 45856729 TCCTCCACCTCCTGAGCTCAATTGATCCTCCCACCTTAGCCTCCCAAAATCCTGGGATTACAGGC TCCTCCACCTCCTGAGCTCAATTGATCCTCCCCCCTTAGCCTCCCAAAATCCTGGGATTACAGGC T G SYMPK Ensembl:ENSG00000125755 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs896509827 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92180,RMVar_hsa_circ_195447 14804 RMVar_ID_14804 Human_SNP_ID_667327479 A-to-I Human chr19 - 45856791 45856791 45856791 GAGACAGGGTGTTGCTCTGTCCGCAGGCTGGAATGCAGTGGTAGGGATCACAGCTCACTGCATCC GAGACAGGGTGTTGCTCTGTCCGCAGGCTGGAGTGCAGTGGTAGGGATCACAGCTCACTGCATCC T C SYMPK Ensembl:ENSG00000125755 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1238164820 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17568127,Human_RBP_ID_17928066 RMVar_hsa_circ_92180,RMVar_hsa_circ_195447 14805 RMVar_ID_14805 Human_SNP_ID_667327487 A-to-I Human chr19 - 45856818 45856816 45856818 GCCACTGCACCTGGCCTGTTTGTTTCTGAGACAGGGTGTTGCTCTGTCCGCAGGCTGGAATGCAG GCCACTGCACCTGGCCTGTTTGTTTCTGAGAC__GGTGTTGCTCTGTCCGCAGGCTGGAATGCAG CCT C SYMPK Ensembl:ENSG00000125755 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1349895822 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_6774097,Human_RBP_ID_13477223,Human_RBP_ID_17568127 RMVar_hsa_circ_92180,RMVar_hsa_circ_195447 14806 RMVar_ID_14806 Human_SNP_ID_667327504 A-to-I Human chr19 - 45856900 45856900 45856900 GTTGGCCAGTCTGGTCTCGAACTCCTGACCTCAGGTGTTCTGCCTACCTCAGCCTCCCAAGGTGC GTTGGCCAGTCTGGTCTCGAACTCCTGACCTCGGGTGTTCTGCCTACCTCAGCCTCCCAAGGTGC T C SYMPK Ensembl:ENSG00000125755 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1241557365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23179230 RMVar_hsa_circ_92180,RMVar_hsa_circ_195447 14807 RMVar_ID_14807 Human_SNP_ID_667327515 A-to-I Human chr19 - 45856945 45856943 45856945 CCTGTCTAATTTGTATGTTTTTAGTAGGGAACAGTGTTTCTCCATGTTGGCCAGTCTGGTCTCGA CCTGTCTAATTTGTATGTTTTTAGTAGGGAAC__TGTTTCTCCATGTTGGCCAGTCTGGTCTCGA ACT A SYMPK Ensembl:ENSG00000125755 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1283870774 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_13477224 RMVar_hsa_circ_92180,RMVar_hsa_circ_195447 14808 RMVar_ID_14808 Human_SNP_ID_667327520 A-to-I Human chr19 - 45856952 45856952 45856952 CACCATGCCTGTCTAATTTGTATGTTTTTAGTAGGGAACAGTGTTTCTCCATGTTGGCCAGTCTG CACCATGCCTGTCTAATTTGTATGTTTTTAGTGGGGAACAGTGTTTCTCCATGTTGGCCAGTCTG T C SYMPK Ensembl:ENSG00000125755 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1298493898 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13477224 RMVar_hsa_circ_92180,RMVar_hsa_circ_195447 14809 RMVar_ID_14809 Human_SNP_ID_667327757 A-to-I Human chr19 - 45857522 45857522 45857522 ACGCCACTGCACTCCAGCCTGGGCGACAGTGCAAGACTCCATCTCAAAAAAAGAAAAAAGTATCA ACGCCACTGCACTCCAGCCTGGGCGACAGTGCGAGACTCCATCTCAAAAAAAGAAAAAAGTATCA T C SYMPK Ensembl:ENSG00000125755 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1178077346 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92180,RMVar_hsa_circ_195447 14810 RMVar_ID_14810 Human_SNP_ID_667327923 A-to-I Human chr19 - 45857911 45857911 45857911 ACCTGTAATCCCAGCTACTTGGGAGATGAGGCAGGAGAATTGCTTGAACCTGGGAGGGTGGAGGT ACCTGTAATCCCAGCTACTTGGGAGATGAGGCGGGAGAATTGCTTGAACCTGGGAGGGTGGAGGT T C SYMPK Ensembl:ENSG00000125755 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs193116335 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17568128,Human_RBP_ID_22720489,Human_RBP_ID_25425700 RMVar_hsa_circ_92180,RMVar_hsa_circ_195447 14811 RMVar_ID_14811 Human_SNP_ID_667328130 A-to-I Human chr19 - 45858641 45858641 45858641 CGTGGTGGCACATGCCTGTAATCCCAGCTACTAGGGAGGCTGAGGCAGGAGAATCGCTTGAACTT CGTGGTGGCACATGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACTT T G SYMPK Ensembl:ENSG00000125755 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs911863246 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92180,RMVar_hsa_circ_195447 14812 RMVar_ID_14812 Human_SNP_ID_667328183 A-to-I Human chr19 - 45858787 45858787 45858787 TCGTCGGCCGGGCGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGCGAA TCGTCGGCCGGGCGCGGTGGCTCATGCCTGTAGTCCCAGCACTTTGGGAGGCCAAGGCGGGCGAA T C SYMPK Ensembl:ENSG00000125755 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1480229392 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92180,RMVar_hsa_circ_195447 14813 RMVar_ID_14813 Human_SNP_ID_667328393 A-to-I Human chr19 - 45859553 45859553 45859553 CTCTGTCATCCAGGCTGGAGTGCAGTGGCGCAATCTCGGCTCGCTGCAACGTCTGCCTCCCAGGC CTCTGTCATCCAGGCTGGAGTGCAGTGGCGCAGTCTCGGCTCGCTGCAACGTCTGCCTCCCAGGC T C SYMPK Ensembl:ENSG00000125755 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs887853347 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13477309 RMVar_hsa_circ_92180,RMVar_hsa_circ_195447 14814 RMVar_ID_14814 Human_SNP_ID_667328637 A-to-I Human chr19 - 45860293 45860293 45860293 CCACCATGCCTGGCTAATTTTTTTGTATTTTTAGTAGAGATGAGGTTTCACCATGTTGGCCAGAC CCACCATGCCTGGCTAATTTTTTTGTATTTTTGGTAGAGATGAGGTTTCACCATGTTGGCCAGAC T C SYMPK Ensembl:ENSG00000125755 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1330509059 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92180,RMVar_hsa_circ_195447 14815 RMVar_ID_14815 Human_SNP_ID_667328751 A-to-I Human chr19 - 45860574 45860574 45860574 TTAATTCATTTAAACCTTGGTGTCTGAGGTTTAAATGAGTTAATATGTATATCTTAGAATTGTGC TTAATTCATTTAAACCTTGGTGTCTGAGGTTTCAATGAGTTAATATGTATATCTTAGAATTGTGC T G SYMPK Ensembl:ENSG00000125755 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs747043314 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92180,RMVar_hsa_circ_195447 14816 RMVar_ID_14816 Human_SNP_ID_667328761 A-to-I Human chr19 - 45860613 45860613 45860613 TAAACCTAACTCATGTATATTAATTCTAATATATACATATTAATTCATTTAAACCTTGGTGTCTG TAAACCTAACTCATGTATATTAATTCTAATATGTACATATTAATTCATTTAAACCTTGGTGTCTG T C SYMPK Ensembl:ENSG00000125755 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1328825917 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92180,RMVar_hsa_circ_195447 14817 RMVar_ID_14817 Human_SNP_ID_667328762 A-to-I Human chr19 - 45860615 45860615 45860615 TGTAAACCTAACTCATGTATATTAATTCTAATATATACATATTAATTCATTTAAACCTTGGTGTC TGTAAACCTAACTCATGTATATTAATTCTAATGTATACATATTAATTCATTTAAACCTTGGTGTC T C SYMPK Ensembl:ENSG00000125755 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1266614620 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92180,RMVar_hsa_circ_195447 14818 RMVar_ID_14818 Human_SNP_ID_667328790 A-to-I Human chr19 - 45860729 45860729 45860729 TGAGGTAGGAGGATCGCCTGAGCCCGGGAGGCAGAGATTGCGGTGAGCTGAGATTGCGGCACTGC TGAGGTAGGAGGATCGCCTGAGCCCGGGAGGCGGAGATTGCGGTGAGCTGAGATTGCGGCACTGC T C SYMPK Ensembl:ENSG00000125755 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs906948846 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13477365,Human_RBP_ID_23309785 RMVar_hsa_circ_92180,RMVar_hsa_circ_195447 14819 RMVar_ID_14819 Human_SNP_ID_667328791 A-to-I Human chr19 - 45860729 45860729 45860729 TGAGGTAGGAGGATCGCCTGAGCCCGGGAGGCAGAGATTGCGGTGAGCTGAGATTGCGGCACTGC TGAGGTAGGAGGATCGCCTGAGCCCGGGAGGCCGAGATTGCGGTGAGCTGAGATTGCGGCACTGC T G SYMPK Ensembl:ENSG00000125755 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs906948846 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13477365,Human_RBP_ID_23309785 RMVar_hsa_circ_92180,RMVar_hsa_circ_195447 14820 RMVar_ID_14820 Human_SNP_ID_667328798 A-to-I Human chr19 - 45860741 45860741 45860741 TACTTGGGAAAATGAGGTAGGAGGATCGCCTGAGCCCGGGAGGCAGAGATTGCGGTGAGCTGAGA TACTTGGGAAAATGAGGTAGGAGGATCGCCTGGGCCCGGGAGGCAGAGATTGCGGTGAGCTGAGA T C SYMPK Ensembl:ENSG00000125755 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1315729160 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6774148,Human_RBP_ID_13477365,Human_RBP_ID_23309785 RMVar_hsa_circ_92180,RMVar_hsa_circ_195447 14821 RMVar_ID_14821 Human_SNP_ID_667329114 A-to-I Human chr19 - 45861879 45861879 45861879 CACCACACCCAGGTAATTTTTATATTTTTAGTAGAGACGGGGTTTCTCTGTGTTGGCCAGGCTGG CACCACACCCAGGTAATTTTTATATTTTTAGTGGAGACGGGGTTTCTCTGTGTTGGCCAGGCTGG T C SYMPK Ensembl:ENSG00000125755 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs12463086 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13477416 RMVar_hsa_circ_92180,RMVar_hsa_circ_195447 14822 RMVar_ID_14822 Human_SNP_ID_667329117 A-to-I Human chr19 - 45861890 45861890 45861890 CAAACGTGCCCCACCACACCCAGGTAATTTTTATATTTTTAGTAGAGACGGGGTTTCTCTGTGTT CAAACGTGCCCCACCACACCCAGGTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCTCTGTGTT T C SYMPK Ensembl:ENSG00000125755 Protein coding intron GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs1568630830 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13477417 RMVar_hsa_circ_92180,RMVar_hsa_circ_195447 14823 RMVar_ID_14823 Human_SNP_ID_667329137 A-to-I Human chr19 - 45861950 45861950 45861950 ACCTCCACCTCCCTGGTTCAAGTGATTCTCCCACCCCAGCCTCTCGAGTAGCTGGGATTACAAAC ACCTCCACCTCCCTGGTTCAAGTGATTCTCCCTCCCCAGCCTCTCGAGTAGCTGGGATTACAAAC T A SYMPK Ensembl:ENSG00000125755 Protein coding intron GSE47997;GSE126723:GSM3611827,GSM3611828,GSM3611829 K562 cells&HepG2 cells;Bronchiolar epithelium,BEP2D cell line - 23474544,31158229 RNA-Seq:(High) rs533954652 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2021362,Human_Splice_Rec_2021363 RMVar_hsa_circ_92180,RMVar_hsa_circ_195447 14824 RMVar_ID_14824 Human_SNP_ID_667329138 A-to-I Human chr19 - 45861950 45861950 45861950 ACCTCCACCTCCCTGGTTCAAGTGATTCTCCCACCCCAGCCTCTCGAGTAGCTGGGATTACAAAC ACCTCCACCTCCCTGGTTCAAGTGATTCTCCCCCCCCAGCCTCTCGAGTAGCTGGGATTACAAAC T G SYMPK Ensembl:ENSG00000125755 Protein coding intron GSE47997;GSE126723:GSM3611827,GSM3611828,GSM3611829 K562 cells&HepG2 cells;Bronchiolar epithelium,BEP2D cell line - 23474544,31158229 RNA-Seq:(High) rs533954652 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2021362,Human_Splice_Rec_2021363 RMVar_hsa_circ_92180,RMVar_hsa_circ_195447 14825 RMVar_ID_14825 Human_SNP_ID_667329146 A-to-I Human chr19 - 45861982 45861982 45861982 CGCCCAGGCTGGCACGATCCCAGTTCACTGCAACCTCCACCTCCCTGGTTCAAGTGATTCTCCCA CGCCCAGGCTGGCACGATCCCAGTTCACTGCAGCCTCCACCTCCCTGGTTCAAGTGATTCTCCCA T C SYMPK Ensembl:ENSG00000125755 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs573833415 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13477418 Human_Splice_Rec_2021362,Human_Splice_Rec_2021363 RMVar_hsa_circ_92180,RMVar_hsa_circ_195447 14826 RMVar_ID_14826 Human_SNP_ID_667329148 A-to-I Human chr19 - 45861988 45861988 45861988 CTCTGTCGCCCAGGCTGGCACGATCCCAGTTCACTGCAACCTCCACCTCCCTGGTTCAAGTGATT CTCTGTCGCCCAGGCTGGCACGATCCCAGTTCGCTGCAACCTCCACCTCCCTGGTTCAAGTGATT T C SYMPK Ensembl:ENSG00000125755 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs542291045 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13477418 Human_Splice_Rec_2021362,Human_Splice_Rec_2021363 RMVar_hsa_circ_92180,RMVar_hsa_circ_195447 14827 RMVar_ID_14827 Human_SNP_ID_667329149 A-to-I Human chr19 - 45861988 45861988 45861988 CTCTGTCGCCCAGGCTGGCACGATCCCAGTTCACTGCAACCTCCACCTCCCTGGTTCAAGTGATT CTCTGTCGCCCAGGCTGGCACGATCCCAGTTCCCTGCAACCTCCACCTCCCTGGTTCAAGTGATT T G SYMPK Ensembl:ENSG00000125755 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs542291045 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13477418 Human_Splice_Rec_2021362,Human_Splice_Rec_2021363 RMVar_hsa_circ_92180,RMVar_hsa_circ_195447 14828 RMVar_ID_14828 Human_SNP_ID_667329196 A-to-I Human chr19 - 45862151 45862151 45862151 ATGCAACTCTAAAAAGGAATGAGGTAGATAAAAGGAAATGATGAAAATCTCTATACACTGATATA ATGCAACTCTAAAAAGGAATGAGGTAGATAAATGGAAATGATGAAAATCTCTATACACTGATATA T A SYMPK Ensembl:ENSG00000125755 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1373250994 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13477425 RMVar_hsa_circ_92180,RMVar_hsa_circ_195447 14829 RMVar_ID_14829 Human_SNP_ID_667329197 A-to-I Human chr19 - 45862151 45862151 45862151 ATGCAACTCTAAAAAGGAATGAGGTAGATAAAAGGAAATGATGAAAATCTCTATACACTGATATA ATGCAACTCTAAAAAGGAATGAGGTAGATAAACGGAAATGATGAAAATCTCTATACACTGATATA T G SYMPK Ensembl:ENSG00000125755 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1373250994 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13477425 RMVar_hsa_circ_92180,RMVar_hsa_circ_195447 14830 RMVar_ID_14830 Human_SNP_ID_667329219 A-to-I Human chr19 - 45862243 45862243 45862243 TTCATCATAGCAAAAGGCTACACGCATCCCAAATGTTCTTAAATAAGAAGATTGGCTGAAAGAAA TTCATCATAGCAAAAGGCTACACGCATCCCAAGTGTTCTTAAATAAGAAGATTGGCTGAAAGAAA T C SYMPK Ensembl:ENSG00000125755 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1379249550 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13477430 RMVar_hsa_circ_92180,RMVar_hsa_circ_195447 14831 RMVar_ID_14831 Human_SNP_ID_667338455 A-to-I Human chr19 - 45893269 45893269 45893269 CACCACACCCGGCCTATTTTTATTTTTGAGACAGAGTCTCGCTCTGTTGCCCAGGCTGGAGTGCA CACCACACCCGGCCTATTTTTATTTTTGAGACGGAGTCTCGCTCTGTTGCCCAGGCTGGAGTGCA T C MYPOP Ensembl:ENSG00000176182 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1261173403 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91019,RMVar_hsa_circ_195449 14832 RMVar_ID_14832 Human_SNP_ID_667414841 A-to-I Human chr19 - 46193024 46193024 46193024 CAGCACCCGGCTAATTTTTGTAATTTTTTAGTAGAGATAGGATTTCACCATGTTTTCCAGGCTGG CAGCACCCGGCTAATTTTTGTAATTTTTTAGTGGAGATAGGATTTCACCATGTTTTCCAGGCTGG T C IGFL2-AS1 Ensembl:ENSG00000268621 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs770565131 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105903,RMVar_hsa_circ_195459,RMVar_hsa_circ_95644,RMVar_hsa_circ_195458 14833 RMVar_ID_14833 Human_SNP_ID_667414857 A-to-I Human chr19 - 46193110 46193110 46193110 TTGGCTCACTGCAACTTCCACCTCTCGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGC TTGGCTCACTGCAACTTCCACCTCTCGGGTTCCAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGC T G IGFL2-AS1 Ensembl:ENSG00000268621 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs894796441 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105903,RMVar_hsa_circ_195459,RMVar_hsa_circ_95644,RMVar_hsa_circ_195458 14834 RMVar_ID_14834 Human_SNP_ID_667415233 A-to-I Human chr19 - 46194637 46194637 46194637 TTGCATTTTTAGTAGAGATGGGGCTTCACCATATTGTCCAGGCTGGTCTTGAATTCCTGATCTCA TTGCATTTTTAGTAGAGATGGGGCTTCACCATGTTGTCCAGGCTGGTCTTGAATTCCTGATCTCA T C IGFL2-AS1 Ensembl:ENSG00000268621 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1226795028 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105903,RMVar_hsa_circ_195459,RMVar_hsa_circ_95644,RMVar_hsa_circ_195458 14835 RMVar_ID_14835 Human_SNP_ID_667416152 A-to-I Human chr19 - 46197750 46197750 46197750 AGGAGGGAGGATCGTTTGAACCCAAGAGTTTAAGACCAGCCTGAACAACATGCTGAAACCCCGTC AGGAGGGAGGATCGTTTGAACCCAAGAGTTTACGACCAGCCTGAACAACATGCTGAAACCCCGTC T G IGFL2-AS1 Ensembl:ENSG00000268621 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1258395513 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23279240 RMVar_hsa_circ_105903,RMVar_hsa_circ_195459,RMVar_hsa_circ_95644,RMVar_hsa_circ_195458 14836 RMVar_ID_14836 Human_SNP_ID_667446785 A-to-I Human chr19 + 46313360 46313360 46313360 TTTTTTGCTTTTTAAATTTTGATGTGGCTCACACCTGTAAATCCCAGAACTTTGGGAGGCCAGGG TTTTTTGCTTTTTAAATTTTGATGTGGCTCACGCCTGTAAATCCCAGAACTTTGGGAGGCCAGGG A G HIF3A Ensembl:ENSG00000124440 Protein coding exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs910212911 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60724 14837 RMVar_ID_14837 Human_SNP_ID_667446989 A-to-I Human chr19 + 46313905 46313905 46313905 TCTGGTCTCGAACTCCTGACCTCAGGTGATCCACCCCCCTCAGCCTCCCAAAGTGTTGGGATTAC TCTGGTCTCGAACTCCTGACCTCAGGTGATCCTCCCCCCTCAGCCTCCCAAAGTGTTGGGATTAC A T HIF3A Ensembl:ENSG00000124440 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1467576486 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60724 14838 RMVar_ID_14838 Human_SNP_ID_667448236 A-to-I Human chr19 + 46319054 46319054 46319054 TGTGAACCACTACACAGCAGTGCTTGATGAGGATATATTTGTGGAATGATGAATGAGTTAACTGA TGTGAACCACTACACAGCAGTGCTTGATGAGGTTATATTTGTGGAATGATGAATGAGTTAACTGA A T HIF3A Ensembl:ENSG00000124440 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs562159584 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23801708 RMVar_hsa_circ_60724 14839 RMVar_ID_14839 Human_SNP_ID_667463463 A-to-I Human chr19 + 46379123 46379123 46379123 GTCACCAGGGTAGAGTGCAGTGGCGCAATCTCAGCTCACTGCAACCTCTGTGTCCCAGATTCAAG GTCACCAGGGTAGAGTGCAGTGGCGCAATCTCGGCTCACTGCAACCTCTGTGTCCCAGATTCAAG A G PPP5C Ensembl:ENSG00000011485 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs200683474 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113173,RMVar_hsa_circ_372962,RMVar_hsa_circ_195463,RMVar_hsa_circ_195462 14840 RMVar_ID_14840 Human_SNP_ID_667465268 A-to-I Human chr19 + 46386712 46386712 46386712 ATAGCTCACTGCAGCCTCTGCTTCGTGGGCTCAAGTGATCCTCTGGCCTCAGCCTCCCAAGTAGC ATAGCTCACTGCAGCCTCTGCTTCGTGGGCTCTAGTGATCCTCTGGCCTCAGCCTCCCAAGTAGC A T PPP5C Ensembl:ENSG00000011485 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1045265911 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_372962,RMVar_hsa_circ_195462 14841 RMVar_ID_14841 Human_SNP_ID_667465270 A-to-I Human chr19 + 46386730 46386730 46386730 TGCTTCGTGGGCTCAAGTGATCCTCTGGCCTCAGCCTCCCAAGTAGCTGGCACTATAGGCACGCA TGCTTCGTGGGCTCAAGTGATCCTCTGGCCTCGGCCTCCCAAGTAGCTGGCACTATAGGCACGCA A G PPP5C Ensembl:ENSG00000011485 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1408762414 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_372962,RMVar_hsa_circ_195462 14842 RMVar_ID_14842 Human_SNP_ID_667511691 A-to-I Human chr19 - 46547678 46547678 46547678 CACCAGGCCCAGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATATTGACCAGGCTGA CACCAGGCCCAGCTAATTTTTGTATTTTTAGTGGAGACAGGGTTTCACCATATTGACCAGGCTGA T C PPP5D1,AC093503.1 Ensembl:ENSG00000230510,Ensembl:ENSG00000268423 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs570577822 Functional Loss SNV dbSNP153 33..33 33 - - - 14843 RMVar_ID_14843 Human_SNP_ID_667545767 A-to-I Human chr19 - 46676872 46676872 46676872 TATTTTTAGTAGAGACAGGGTTTCGCCATGTTAGCCAGGCTGGTCTTGAACTCCTGACCTCAAGT TATTTTTAGTAGAGACAGGGTTTCGCCATGTTGGCCAGGCTGGTCTTGAACTCCTGACCTCAAGT T C PRKD2 Ensembl:ENSG00000105287 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs906650865 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87900,RMVar_hsa_circ_195482 14844 RMVar_ID_14844 Human_SNP_ID_667547498 A-to-I Human chr19 - 46682845 46682845 46682845 CAAAAATTAGTCAGGTGTGATGGTGTGTGCCTATAATCCCAGTTACTAGGGAGGTTGAGGTGGGA CAAAAATTAGTCAGGTGTGATGGTGTGTGCCTGTAATCCCAGTTACTAGGGAGGTTGAGGTGGGA T C PRKD2 Ensembl:ENSG00000105287 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs543584776 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123336,RMVar_hsa_circ_31591,RMVar_hsa_circ_294657,RMVar_hsa_circ_372923,RMVar_hsa_circ_195483,RMVar_hsa_circ_306538,RMVar_hsa_circ_65359,RMVar_hsa_circ_195485,RMVar_hsa_circ_31042,RMVar_hsa_circ_195486,RMVar_hsa_circ_195484 14845 RMVar_ID_14845 Human_SNP_ID_667547630 A-to-I Human chr19 - 46683368 46683368 46683368 TGAAATCAGGCTGGGCACAGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCCAAGGTTGGT TGAAATCAGGCTGGGCACAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGTTGGT T C PRKD2 Ensembl:ENSG00000105287 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1307533748 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123336,RMVar_hsa_circ_31591,RMVar_hsa_circ_294657,RMVar_hsa_circ_372923,RMVar_hsa_circ_195483,RMVar_hsa_circ_306538,RMVar_hsa_circ_65359,RMVar_hsa_circ_195485,RMVar_hsa_circ_31042,RMVar_hsa_circ_195486,RMVar_hsa_circ_195484 14846 RMVar_ID_14846 Human_SNP_ID_667547912 A-to-I Human chr19 - 46684459 46684459 46684459 AAATTAGCCAGGTGTGGTGGCATTCACCTGTAATCCCAGCTACTGGGGAGGCTGAGGCACAAGAA AAATTAGCCAGGTGTGGTGGCATTCACCTGTATTCCCAGCTACTGGGGAGGCTGAGGCACAAGAA T A PRKD2 Ensembl:ENSG00000105287 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1271574170 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123336,RMVar_hsa_circ_31591,RMVar_hsa_circ_294657,RMVar_hsa_circ_372923,RMVar_hsa_circ_195483,RMVar_hsa_circ_306538,RMVar_hsa_circ_65359,RMVar_hsa_circ_195485,RMVar_hsa_circ_31042,RMVar_hsa_circ_195486,RMVar_hsa_circ_195484 14847 RMVar_ID_14847 Human_SNP_ID_667547913 A-to-I Human chr19 - 46684460 46684460 46684460 AAAATTAGCCAGGTGTGGTGGCATTCACCTGTAATCCCAGCTACTGGGGAGGCTGAGGCACAAGA AAAATTAGCCAGGTGTGGTGGCATTCACCTGTGATCCCAGCTACTGGGGAGGCTGAGGCACAAGA T C PRKD2 Ensembl:ENSG00000105287 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1387270375 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123336,RMVar_hsa_circ_31591,RMVar_hsa_circ_294657,RMVar_hsa_circ_372923,RMVar_hsa_circ_195483,RMVar_hsa_circ_306538,RMVar_hsa_circ_65359,RMVar_hsa_circ_195485,RMVar_hsa_circ_31042,RMVar_hsa_circ_195486,RMVar_hsa_circ_195484 14848 RMVar_ID_14848 Human_SNP_ID_667548321 A-to-I Human chr19 - 46685943 46685943 46685943 TCCAGACTTTATTATTTATGTATTTTTGAGACAGAGTCTCGCTTTGTTGCCCAGGCTGGAGCGCA TCCAGACTTTATTATTTATGTATTTTTGAGACTGAGTCTCGCTTTGTTGCCCAGGCTGGAGCGCA T A PRKD2 Ensembl:ENSG00000105287 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1314172276 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123336,RMVar_hsa_circ_31591,RMVar_hsa_circ_372923,RMVar_hsa_circ_195483,RMVar_hsa_circ_306538,RMVar_hsa_circ_65359,RMVar_hsa_circ_195485,RMVar_hsa_circ_31042,RMVar_hsa_circ_195484 14849 RMVar_ID_14849 Human_SNP_ID_667548412 A-to-I Human chr19 - 46686341 46686339 46686341 CATGAGCCATTACACCTGGCTAATTTTTTTTTATGTTTTTGTAGAGACAGGGTCTTGCCATGTTG CATGAGCCATTACACCTGGCTAATTTTTTTTT__GTTTTTGTAGAGACAGGGTCTTGCCATGTTG CAT C PRKD2 Ensembl:ENSG00000105287 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs941562387 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_123336,RMVar_hsa_circ_31591,RMVar_hsa_circ_372923,RMVar_hsa_circ_195483,RMVar_hsa_circ_306538,RMVar_hsa_circ_65359,RMVar_hsa_circ_195485,RMVar_hsa_circ_31042,RMVar_hsa_circ_195484 14850 RMVar_ID_14850 Human_SNP_ID_667548685 A-to-I Human chr19 - 46687292 46687292 46687292 GACCTCCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCTGAGACAACAGGCATCAG GACCTCCCGGGTTCAAGCAATTCTCCTGCCTCTGCCTCCTGAGTAGCTGAGACAACAGGCATCAG T A PRKD2 Ensembl:ENSG00000105287 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1459746861 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123336,RMVar_hsa_circ_31591,RMVar_hsa_circ_372923,RMVar_hsa_circ_195483,RMVar_hsa_circ_306538,RMVar_hsa_circ_65359,RMVar_hsa_circ_195485,RMVar_hsa_circ_31042,RMVar_hsa_circ_195484 14851 RMVar_ID_14851 Human_SNP_ID_667548868 A-to-I Human chr19 - 46688098 46688098 46688098 ATCGCTTGAAGCCAGGAGTTGGAGACCAGCCTAGGCGACATAGTGAGATCCCACCTCTACAAAAA ATCGCTTGAAGCCAGGAGTTGGAGACCAGCCTTGGCGACATAGTGAGATCCCACCTCTACAAAAA T A PRKD2 Ensembl:ENSG00000105287 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1490106659 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123336,RMVar_hsa_circ_31591,RMVar_hsa_circ_372923,RMVar_hsa_circ_195483,RMVar_hsa_circ_306538,RMVar_hsa_circ_65359,RMVar_hsa_circ_195485,RMVar_hsa_circ_31042,RMVar_hsa_circ_195484 14852 RMVar_ID_14852 Human_SNP_ID_667552404 A-to-I Human chr19 - 46701434 46701434 46701434 GTATTTTTAGTAGAGACGAGGTTTTACCATGTAGGGCAGGCTGGTTTCGAACTCCTGACCTCAAA GTATTTTTAGTAGAGACGAGGTTTTACCATGTTGGGCAGGCTGGTTTCGAACTCCTGACCTCAAA T A PRKD2 Ensembl:ENSG00000105287 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1471935860 Functional Loss SNV dbSNP153 33..33 33 - - - 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_317531 14853 RMVar_ID_14853 Human_SNP_ID_667552706 A-to-I Human chr19 - 46702312 46702312 46702312 AATCAGGTCAGGGGCAGTAGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTTAGGTGGGTGGA AATCAGGTCAGGGGCAGTAGCTCACACCTGTAGTCCCAGCACTTTGGGAGGCTTAGGTGGGTGGA T C PRKD2 Ensembl:ENSG00000105287 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1178403828 Functional Loss SNV dbSNP153 33..33 33 - - - 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_317531 14854 RMVar_ID_14854 Human_SNP_ID_667553982 A-to-I Human chr19 - 46707034 46707034 46707034 GAAAAATTAGCTGGGTGTGGTGGCGGGTACCTATAATCCCAGCTACTCGGGAGGCTGAGGCAGGA GAAAAATTAGCTGGGTGTGGTGGCGGGTACCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGA T C PRKD2 Ensembl:ENSG00000105287 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs560972619 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_372923,RMVar_hsa_circ_31042,RMVar_hsa_circ_195484,RMVar_hsa_circ_24491,RMVar_hsa_circ_343379,RMVar_hsa_circ_195491,RMVar_hsa_circ_317531,RMVar_hsa_circ_327876 14855 RMVar_ID_14855 Human_SNP_ID_667554231 A-to-I Human chr19 - 46708015 46708015 46708015 CAGCTCACCACAACCTCCACTTCCCAGGCTCAAGCGATTCTCCTGCCTCAGCCTACCGAGTAGCT CAGCTCACCACAACCTCCACTTCCCAGGCTCAGGCGATTCTCCTGCCTCAGCCTACCGAGTAGCT T C PRKD2 Ensembl:ENSG00000105287 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1444810508 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_372923,RMVar_hsa_circ_31042,RMVar_hsa_circ_195484,RMVar_hsa_circ_24491,RMVar_hsa_circ_343379,RMVar_hsa_circ_195491,RMVar_hsa_circ_317531,RMVar_hsa_circ_327876 14856 RMVar_ID_14856 Human_SNP_ID_667554608 A-to-I Human chr19 - 46709164 46709164 46709164 TGAGACCACCCTGGCCAACATGGTGAAACCCCATCTCTCCTAAAAATACAAAAATTAGCGGGCGT TGAGACCACCCTGGCCAACATGGTGAAACCCCCTCTCTCCTAAAAATACAAAAATTAGCGGGCGT T G PRKD2 Ensembl:ENSG00000105287 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1184731861 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_372923,RMVar_hsa_circ_31042,RMVar_hsa_circ_195484,RMVar_hsa_circ_24491,RMVar_hsa_circ_343379,RMVar_hsa_circ_195491,RMVar_hsa_circ_317531,RMVar_hsa_circ_327876 14857 RMVar_ID_14857 Human_SNP_ID_667555511 A-to-I Human chr19 - 46712375 46712375 46712375 TACCACACGTGGCTAATTTTTGTATTTTTAGTAGAGACGGGATTTCACCTTGTTGGCCAGGCTGG TACCACACGTGGCTAATTTTTGTATTTTTAGTTGAGACGGGATTTCACCTTGTTGGCCAGGCTGG T A PRKD2 Ensembl:ENSG00000105287 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1250679446 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_372923,RMVar_hsa_circ_195484,RMVar_hsa_circ_24491 14858 RMVar_ID_14858 Human_SNP_ID_667562144 A-to-I Human chr19 - 46734700 46734700 46734700 AGATCGTGCCACTGCACTCCAGCCTGGGCGACAGAGCAAGAGTCTGTCTTAACAACAACAAAAAA AGATCGTGCCACTGCACTCCAGCCTGGGCGACGGAGCAAGAGTCTGTCTTAACAACAACAAAAAA T C STRN4 Ensembl:ENSG00000090372 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1480239295 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21929983 RMVar_hsa_circ_82942,RMVar_hsa_circ_195494,RMVar_hsa_circ_120653,RMVar_hsa_circ_195499,RMVar_hsa_circ_5612,RMVar_hsa_circ_358829,RMVar_hsa_circ_359601 14859 RMVar_ID_14859 Human_SNP_ID_667562296 A-to-I Human chr19 - 46735134 46735134 46735134 ACCTGGCTAATTTTTGTATTTTTAGTAAAGACAGCGTTTTACCATGTTGGCCAAGCTGGTCTTGA ACCTGGCTAATTTTTGTATTTTTAGTAAAGACGGCGTTTTACCATGTTGGCCAAGCTGGTCTTGA T C STRN4 Ensembl:ENSG00000090372 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1043991031 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82942,RMVar_hsa_circ_195494,RMVar_hsa_circ_120653,RMVar_hsa_circ_195499,RMVar_hsa_circ_5612,RMVar_hsa_circ_358829,RMVar_hsa_circ_359601 14860 RMVar_ID_14860 Human_SNP_ID_667564544 A-to-I Human chr19 - 46743737 46743737 46743737 CACCACCACGCCTGGCTGATTTTTGTATTTTTAGTAGAGATGGGGTTTTGCCACGTTGGTCAGGC CACCACCACGCCTGGCTGATTTTTGTATTTTTCGTAGAGATGGGGTTTTGCCACGTTGGTCAGGC T G STRN4 Ensembl:ENSG00000090372 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167742595 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25426416 RMVar_hsa_circ_120653,RMVar_hsa_circ_195499 14861 RMVar_ID_14861 Human_SNP_ID_667566017 A-to-I Human chr19 + 46748771 46748771 46748771 CGTCTTTTTTTTGTTTGTTTGTTTGTTTTGAGACAGGGTCTCACCCAGGCTAGAGTGAAGTGGAG CGTCTTTTTTTTGTTTGTTTGTTTGTTTTGAGTCAGGGTCTCACCCAGGCTAGAGTGAAGTGGAG A T FKRP Ensembl:ENSG00000181027 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1235645661 Functional Loss SNV dbSNP153 33..33 33 - - - 14862 RMVar_ID_14862 Human_SNP_ID_667566021 A-to-I Human chr19 + 46748796 46748795 46748796 TTTTGAGACAGGGTCTCACCCAGGCTAGAGTGAAGTGGAGCAATCTCGGCTCACTGCAACCTCCG TTTTGAGACAGGGTCTCACCCAGGCTAGAGTG_AGTGGAGCAATCTCGGCTCACTGCAACCTCCG GA G FKRP Ensembl:ENSG00000181027 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1438143020 Functional Loss DEL dbSNP153 33..33 33 - - - Human_Splice_Rec_2022945,Human_Splice_Rec_2022955,Human_Splice_Rec_2022961,Human_Splice_Rec_2023063 14863 RMVar_ID_14863 Human_SNP_ID_667567339 A-to-I Human chr19 + 46754204 46754204 46754204 GGGACCATAGGTGAGTAGCACCACACCCAGCTAATTTTTTATTTTTTGTAGAGATGAAGTCTCCT GGGACCATAGGTGAGTAGCACCACACCCAGCTTATTTTTTATTTTTTGTAGAGATGAAGTCTCCT A T FKRP Ensembl:ENSG00000181027 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1004863212 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13480608 14864 RMVar_ID_14864 Human_SNP_ID_667569780 A-to-I Human chr19 + 46761961 46761961 46761961 TTGGCTCACTGCAGCCTCAACTTCCCAGGCTCAGGCGATTCTCCCACCTCAGCCTCCCGAGTAGC TTGGCTCACTGCAGCCTCAACTTCCCAGGCTCGGGCGATTCTCCCACCTCAGCCTCCCGAGTAGC A G FKRP Ensembl:ENSG00000181027 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1354765907 Functional Loss SNV dbSNP153 33..33 33 - - - 14865 RMVar_ID_14865 Human_SNP_ID_667570051 A-to-I Human chr19 + 46762975 46762975 46762975 GGGAGGCTGAGGCGGGCAGATCACTTGAGGTCAGGAGTTTGAGACCAGCCCAGTCAACATGGTGA GGGAGGCTGAGGCGGGCAGATCACTTGAGGTCGGGAGTTTGAGACCAGCCCAGTCAACATGGTGA A G FKRP Ensembl:ENSG00000181027 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1212073460 Functional Loss SNV dbSNP153 33..33 33 - - - 14866 RMVar_ID_14866 Human_SNP_ID_667573654 A-to-I Human chr19 - 46775998 46775998 46775998 GTGATCACTGCAGCCTCCACCTCCCAGGCTCCAGCGATCCTCCTGCCCCAGCCTCCTGAGTAGCT GTGATCACTGCAGCCTCCACCTCCCAGGCTCCGGCGATCCTCCTGCCCCAGCCTCCTGAGTAGCT T C SLC1A5 Ensembl:ENSG00000105281 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1393094024 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87132,RMVar_hsa_circ_115961,RMVar_hsa_circ_126777,RMVar_hsa_circ_118939,RMVar_hsa_circ_106498,RMVar_hsa_circ_111058,RMVar_hsa_circ_90411,RMVar_hsa_circ_195503,RMVar_hsa_circ_195505,RMVar_hsa_circ_195507,RMVar_hsa_circ_195508,RMVar_hsa_circ_195506,RMVar_hsa_circ_195504,RMVar_hsa_circ_195502 14867 RMVar_ID_14867 Human_SNP_ID_667573756 A-to-I Human chr19 - 46776373 46776372 46776373 TGAAACCCCATCTCCACTAAAAATACAAAAAAATTAGCCGGGTATGGTGGTGTACGCCTGTCCTG TGAAACCCCATCTCCACTAAAAATACAAAAAA_TTAGCCGGGTATGGTGGTGTACGCCTGTCCTG AT A SLC1A5 Ensembl:ENSG00000105281 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1195152851 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_17928370 RMVar_hsa_circ_87132,RMVar_hsa_circ_115961,RMVar_hsa_circ_126777,RMVar_hsa_circ_118939,RMVar_hsa_circ_106498,RMVar_hsa_circ_111058,RMVar_hsa_circ_90411,RMVar_hsa_circ_195503,RMVar_hsa_circ_195505,RMVar_hsa_circ_195507,RMVar_hsa_circ_195508,RMVar_hsa_circ_195506,RMVar_hsa_circ_195504,RMVar_hsa_circ_195502 14868 RMVar_ID_14868 Human_SNP_ID_667574811 A-to-I Human chr19 - 46780127 46780127 46780127 AACTGGGTGGCCCAGTACGGAGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCTGAGGCAGGC AACTGGGTGGCCCAGTACGGAGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGC T C SLC1A5 Ensembl:ENSG00000105281 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs894754464 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17567751,Human_RBP_ID_22720493,Human_RBP_ID_25426481 RMVar_hsa_circ_6063,RMVar_hsa_circ_126777,RMVar_hsa_circ_118939,RMVar_hsa_circ_106498,RMVar_hsa_circ_111058,RMVar_hsa_circ_90411,RMVar_hsa_circ_89403,RMVar_hsa_circ_195503,RMVar_hsa_circ_195505,RMVar_hsa_circ_195506,RMVar_hsa_circ_195504,RMVar_hsa_circ_370591,RMVar_hsa_circ_195502,RMVar_hsa_circ_285167,RMVar_hsa_circ_195513,RMVar_hsa_circ_80819,RMVar_hsa_circ_195514,RMVar_hsa_circ_195515,RMVar_hsa_circ_195512,RMVar_hsa_circ_124836,RMVar_hsa_circ_371442,RMVar_hsa_circ_195516,RMVar_hsa_circ_195517 14869 RMVar_ID_14869 Human_SNP_ID_667574910 A-to-I Human chr19 - 46780495 46780495 46780495 AATATTAGCTGGGAATGGTGGTGTACACCTTTAATCCTAGCTACTACTCAGGAGGCTGAGGCATG AATATTAGCTGGGAATGGTGGTGTACACCTTTGATCCTAGCTACTACTCAGGAGGCTGAGGCATG T C SLC1A5 Ensembl:ENSG00000105281 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs373274268 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6063,RMVar_hsa_circ_126777,RMVar_hsa_circ_118939,RMVar_hsa_circ_106498,RMVar_hsa_circ_111058,RMVar_hsa_circ_90411,RMVar_hsa_circ_89403,RMVar_hsa_circ_195503,RMVar_hsa_circ_195505,RMVar_hsa_circ_195506,RMVar_hsa_circ_195504,RMVar_hsa_circ_370591,RMVar_hsa_circ_195502,RMVar_hsa_circ_285167,RMVar_hsa_circ_195513,RMVar_hsa_circ_80819,RMVar_hsa_circ_195514,RMVar_hsa_circ_195515,RMVar_hsa_circ_195512,RMVar_hsa_circ_124836,RMVar_hsa_circ_371442,RMVar_hsa_circ_195516,RMVar_hsa_circ_195517 14870 RMVar_ID_14870 Human_SNP_ID_667574924 A-to-I Human chr19 - 46780585 46780585 46780585 GGGAGGCTGAGGGGGGAGGATTGCTTGAGGCCAGGAGTTAGAGACTAGCCTGGTCAACATGGCGA GGGAGGCTGAGGGGGGAGGATTGCTTGAGGCCGGGAGTTAGAGACTAGCCTGGTCAACATGGCGA T C SLC1A5 Ensembl:ENSG00000105281 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1285731722 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6063,RMVar_hsa_circ_126777,RMVar_hsa_circ_118939,RMVar_hsa_circ_106498,RMVar_hsa_circ_111058,RMVar_hsa_circ_90411,RMVar_hsa_circ_89403,RMVar_hsa_circ_195503,RMVar_hsa_circ_195505,RMVar_hsa_circ_195506,RMVar_hsa_circ_195504,RMVar_hsa_circ_370591,RMVar_hsa_circ_195502,RMVar_hsa_circ_285167,RMVar_hsa_circ_195513,RMVar_hsa_circ_80819,RMVar_hsa_circ_195514,RMVar_hsa_circ_195515,RMVar_hsa_circ_195512,RMVar_hsa_circ_124836,RMVar_hsa_circ_371442,RMVar_hsa_circ_195516,RMVar_hsa_circ_195517 14871 RMVar_ID_14871 Human_SNP_ID_667575294 A-to-I Human chr19 - 46782123 46782123 46782123 TTTGGGAGGAGGTGGGTGGATCACTTGAGATCAGGAGTTCAAAACCAGCCTGGCCAACATGGTGA TTTGGGAGGAGGTGGGTGGATCACTTGAGATCGGGAGTTCAAAACCAGCCTGGCCAACATGGTGA T C SLC1A5 Ensembl:ENSG00000105281 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1419782480 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6063,RMVar_hsa_circ_126777,RMVar_hsa_circ_118939,RMVar_hsa_circ_106498,RMVar_hsa_circ_111058,RMVar_hsa_circ_90411,RMVar_hsa_circ_89403,RMVar_hsa_circ_195503,RMVar_hsa_circ_195505,RMVar_hsa_circ_195506,RMVar_hsa_circ_195504,RMVar_hsa_circ_370591,RMVar_hsa_circ_195502,RMVar_hsa_circ_285167,RMVar_hsa_circ_195513,RMVar_hsa_circ_80819,RMVar_hsa_circ_195514,RMVar_hsa_circ_195515,RMVar_hsa_circ_195512,RMVar_hsa_circ_124836,RMVar_hsa_circ_371442,RMVar_hsa_circ_195516,RMVar_hsa_circ_195517 14872 RMVar_ID_14872 Human_SNP_ID_667593018 A-to-I Human chr19 - 46843432 46843432 46843432 CAGCCATGAGTGACCACGCCTGGCTAATTTTTAAATTTTTCGTAGAGATGGGGTATTGCTATGTT CAGCCATGAGTGACCACGCCTGGCTAATTTTTTAATTTTTCGTAGAGATGGGGTATTGCTATGTT T A AP2S1 Ensembl:ENSG00000042753 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928728077 Functional Loss SNV dbSNP153 33..33 33 - - - 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 14873 RMVar_ID_14873 Human_SNP_ID_667601090 A-to-I Human chr19 + 46871865 46871865 46871865 AGCCAGGCATGGTGGCGGGTGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCA AGCCAGGCATGGTGGCGGGTGCCTGTAATCCCGGCTACTCGGGAGGCTGAGGCAGGAGAATCGCA A G ARHGAP35 Ensembl:ENSG00000160007 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs568310776 Functional Loss SNV dbSNP153 33..33 33 - - - 14874 RMVar_ID_14874 Human_SNP_ID_667657404 A-to-I Human chr19 - 47078716 47078716 47078716 AGCTGGGATTACAGGTGCCAGCCACCATGCCCAGCTGAGTTTTGTATTTTTAGTAGAGACAGGGT AGCTGGGATTACAGGTGCCAGCCACCATGCCCCGCTGAGTTTTGTATTTTTAGTAGAGACAGGGT T G ZC3H4 Ensembl:ENSG00000130749 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs978688849 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 14875 RMVar_ID_14875 Human_SNP_ID_667657434 A-to-I Human chr19 - 47078820 47078820 47078820 GAGTTTCACTCTTTCGCCCAGGCTGAAGTGCAATGGCACCATCTCGGCTCACTGCAACCTCTGCC GAGTTTCACTCTTTCGCCCAGGCTGAAGTGCAGTGGCACCATCTCGGCTCACTGCAACCTCTGCC T C ZC3H4 Ensembl:ENSG00000130749 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs899017115 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 14876 RMVar_ID_14876 Human_SNP_ID_667657710 A-to-I Human chr19 - 47079638 47079638 47079638 CCACCTTGGCCTCCCAAATCGCTGGGATTACAAGTGTGAGCCACAGCGCCTGGCATGCCCCAGGG CCACCTTGGCCTCCCAAATCGCTGGGATTACAGGTGTGAGCCACAGCGCCTGGCATGCCCCAGGG T C ZC3H4 Ensembl:ENSG00000130749 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1350366398 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 14877 RMVar_ID_14877 Human_SNP_ID_667657795 A-to-I Human chr19 - 47079840 47079840 47079840 CTCTGTCACCCAGGCTGGAGTGCAGTGGCACAATCTCGGCTCCCTGCAACCTCTACCTCCTGGGT CTCTGTCACCCAGGCTGGAGTGCAGTGGCACAGTCTCGGCTCCCTGCAACCTCTACCTCCTGGGT T C ZC3H4 Ensembl:ENSG00000130749 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs991452299 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 14878 RMVar_ID_14878 Human_SNP_ID_667658020 A-to-I Human chr19 - 47080636 47080636 47080636 AAAAAATTAGCCAGGTATTGTGGCACATGCCTATGGTCCCAGCTACTCGAGAGGCTGAGGTGGGA AAAAAATTAGCCAGGTATTGTGGCACATGCCTGTGGTCCCAGCTACTCGAGAGGCTGAGGTGGGA T C ZC3H4 Ensembl:ENSG00000130749 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031653658 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 14879 RMVar_ID_14879 Human_SNP_ID_667658118 A-to-I Human chr19 - 47081028 47081028 47081028 TGGCTGGGCTGGGTGCAGTGGTTTATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGCAG TGGCTGGGCTGGGTGCAGTGGTTTATGCCTGTGATCCCAGCACTTTGGGAGGCCAAGGCAGGCAG T C ZC3H4 Ensembl:ENSG00000130749 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1412389008 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 14880 RMVar_ID_14880 Human_SNP_ID_667664261 A-to-I Human chr19 - 47101320 47101320 47101320 ACTCCTGGGCTCAAGCAGTCTGACAGGGTCTCACTCTGTTGCCCAGGCTGGAGGGCAGTGGTGCA ACTCCTGGGCTCAAGCAGTCTGACAGGGTCTCGCTCTGTTGCCCAGGCTGGAGGGCAGTGGTGCA T C ZC3H4 Ensembl:ENSG00000130749 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs767125769 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23179472 RMVar_hsa_circ_111861,RMVar_hsa_circ_195543,RMVar_hsa_circ_95130,RMVar_hsa_circ_195550,RMVar_hsa_circ_195555,RMVar_hsa_circ_105192 14881 RMVar_ID_14881 Human_SNP_ID_667664780 A-to-I Human chr19 - 47103442 47103442 47103442 AAAATTAGCTGGGCATGGTGGTGCATGCTTGTAGTCCCATCTACTTGGGAGGCTGACGTGGGAAG AAAATTAGCTGGGCATGGTGGTGCATGCTTGTGGTCCCATCTACTTGGGAGGCTGACGTGGGAAG T C ZC3H4 Ensembl:ENSG00000130749 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs930807191 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111861,RMVar_hsa_circ_195543,RMVar_hsa_circ_95130,RMVar_hsa_circ_195550,RMVar_hsa_circ_195555,RMVar_hsa_circ_105192 14882 RMVar_ID_14882 Human_SNP_ID_667673343 A-to-I Human chr19 + 47132467 47132467 47132467 TTTTTGTAGGATGGGGTTTTGCCATGTTGCCCAGACTGGTCTTGAACTCCCAAGCTCAAGCGATC TTTTTGTAGGATGGGGTTTTGCCATGTTGCCCGGACTGGTCTTGAACTCCCAAGCTCAAGCGATC A G SAE1 Ensembl:ENSG00000142230 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1454630063 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13482798 14883 RMVar_ID_14883 Human_SNP_ID_667673344 A-to-I Human chr19 + 47132467 47132467 47132467 TTTTTGTAGGATGGGGTTTTGCCATGTTGCCCAGACTGGTCTTGAACTCCCAAGCTCAAGCGATC TTTTTGTAGGATGGGGTTTTGCCATGTTGCCCTGACTGGTCTTGAACTCCCAAGCTCAAGCGATC A T SAE1 Ensembl:ENSG00000142230 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1454630063 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13482798 14884 RMVar_ID_14884 Human_SNP_ID_667674135 A-to-I Human chr19 + 47135553 47135553 47135553 TTTGTAGACAGGGTCTCTCTGTCGCGCAGACTAGAGTGCAGTGGTGTGATCACAACTCACTTCAG TTTGTAGACAGGGTCTCTCTGTCGCGCAGACTGGAGTGCAGTGGTGTGATCACAACTCACTTCAG A G SAE1 Ensembl:ENSG00000142230 Protein coding 5'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1311910643 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13482908 Human_Splice_Rec_2023396,Human_Splice_Rec_2023397 14885 RMVar_ID_14885 Human_SNP_ID_667675658 A-to-I Human chr19 + 47140673 47140673 47140673 CATAAATCAGCCAGGTGCAGTGGTGTGCACCTATAGTCCCAGGACTCAATAGGCCGAGGTGGCGG CATAAATCAGCCAGGTGCAGTGGTGTGCACCTGTAGTCCCAGGACTCAATAGGCCGAGGTGGCGG A G SAE1 Ensembl:ENSG00000142230 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1311431294 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13483053 14886 RMVar_ID_14886 Human_SNP_ID_667675789 A-to-I Human chr19 + 47141141 47141141 47141141 CTCCTGCCTCACTGTCCCGAGTAACTGGGACTACAGGCGCCTGCCACCACGCCTGGCTAATTTTT CTCCTGCCTCACTGTCCCGAGTAACTGGGACTGCAGGCGCCTGCCACCACGCCTGGCTAATTTTT A G SAE1 Ensembl:ENSG00000142230 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs933669970 Functional Loss SNV dbSNP153 33..33 33 - - - 14887 RMVar_ID_14887 Human_SNP_ID_667679825 A-to-I Human chr19 + 47156313 47156313 47156313 AAGCAAAACAAAAAATTTTTTGTATTTTCTCTACTAACAATACAAAAATTAGCTGGGCAAGGTGG AAGCAAAACAAAAAATTTTTTGTATTTTCTCTGCTAACAATACAAAAATTAGCTGGGCAAGGTGG A G SAE1 Ensembl:ENSG00000142230 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1023331664 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9265,RMVar_hsa_circ_44245,RMVar_hsa_circ_300920,RMVar_hsa_circ_337323,RMVar_hsa_circ_195558,RMVar_hsa_circ_56834,RMVar_hsa_circ_363271 14888 RMVar_ID_14888 Human_SNP_ID_667681412 A-to-I Human chr19 + 47162813 47162813 47162813 AGGAGTTTGAGACCAGCCTGGGCAATGTGGCTAAAACCCCTTCTCTACCAAAAATACAAAAATTA AGGAGTTTGAGACCAGCCTGGGCAATGTGGCTGAAACCCCTTCTCTACCAAAAATACAAAAATTA A G SAE1 Ensembl:ENSG00000142230 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs773364244 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17928573 RMVar_hsa_circ_9265,RMVar_hsa_circ_44245,RMVar_hsa_circ_300920,RMVar_hsa_circ_337323,RMVar_hsa_circ_195558,RMVar_hsa_circ_56834,RMVar_hsa_circ_363271 14889 RMVar_ID_14889 Human_SNP_ID_667682881 A-to-I Human chr19 + 47168011 47168011 47168011 GGTCAGGAGTTTGAGACTAGCCTGGGCAATATAGTGAAATCCTGTCTCTACTAAAAATACAAAAA GGTCAGGAGTTTGAGACTAGCCTGGGCAATATGGTGAAATCCTGTCTCTACTAAAAATACAAAAA A G SAE1 Ensembl:ENSG00000142230 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs993855441 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9265,RMVar_hsa_circ_44245,RMVar_hsa_circ_300920,RMVar_hsa_circ_337323,RMVar_hsa_circ_195558,RMVar_hsa_circ_56834,RMVar_hsa_circ_363271 14890 RMVar_ID_14890 Human_SNP_ID_667683667 A-to-I Human chr19 + 47170712 47170711 47170712 TATTTTTTTGTAGAAGCGAAGTTTCTCCATGTAGCCAGGCTGGACTTGAACTCCTGAGCTCTAGT TATTTTTTTGTAGAAGCGAAGTTTCTCCATGT_GCCAGGCTGGACTTGAACTCCTGAGCTCTAGT TA T SAE1 Ensembl:ENSG00000142230 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1568598318 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_8490995,Human_RBP_ID_13483878 RMVar_hsa_circ_44245,RMVar_hsa_circ_337323,RMVar_hsa_circ_56834,RMVar_hsa_circ_195562,RMVar_hsa_circ_336917,RMVar_hsa_circ_347680,RMVar_hsa_circ_118551 14891 RMVar_ID_14891 Human_SNP_ID_667684354 A-to-I Human chr19 + 47173065 47173065 47173065 TTTCTTTTTCCCCAGAGACAGAGTCTTGCTCTATCACCCAGGTAGGAGTGCAGTGGGGCGATCTT TTTCTTTTTCCCCAGAGACAGAGTCTTGCTCTGTCACCCAGGTAGGAGTGCAGTGGGGCGATCTT A G SAE1 Ensembl:ENSG00000142230 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs892332706 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6776073,Human_RBP_ID_17928580,Human_RBP_ID_25427288 RMVar_hsa_circ_44245,RMVar_hsa_circ_337323,RMVar_hsa_circ_56834,RMVar_hsa_circ_195562,RMVar_hsa_circ_336917,RMVar_hsa_circ_347680,RMVar_hsa_circ_118551 14892 RMVar_ID_14892 Human_SNP_ID_667684385 A-to-I Human chr19 + 47173179 47173177 47173180 CACCACCACACCCAGCTAATTTTTGTATTCTTAGTAGAGGCAGGGTTCCACCGTGTTGGCCAGGC CACCACCACACCCAGCTAATTTTTGTATTCT___TAGAGGCAGGGTTCCACCGTGTTGGCCAGGC TTAG T SAE1 Ensembl:ENSG00000142230 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1339632687 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_13483973 RMVar_hsa_circ_44245,RMVar_hsa_circ_337323,RMVar_hsa_circ_56834,RMVar_hsa_circ_195562,RMVar_hsa_circ_336917,RMVar_hsa_circ_347680,RMVar_hsa_circ_118551 14893 RMVar_ID_14893 Human_SNP_ID_667684386 A-to-I Human chr19 + 47173179 47173179 47173179 CACCACCACACCCAGCTAATTTTTGTATTCTTAGTAGAGGCAGGGTTCCACCGTGTTGGCCAGGC CACCACCACACCCAGCTAATTTTTGTATTCTTGGTAGAGGCAGGGTTCCACCGTGTTGGCCAGGC A G SAE1 Ensembl:ENSG00000142230 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1273360784 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13483973 RMVar_hsa_circ_44245,RMVar_hsa_circ_337323,RMVar_hsa_circ_56834,RMVar_hsa_circ_195562,RMVar_hsa_circ_336917,RMVar_hsa_circ_347680,RMVar_hsa_circ_118551 14894 RMVar_ID_14894 Human_SNP_ID_667685612 A-to-I Human chr19 + 47177570 47177570 47177570 GTTTGTACAGATTGGGGCAGGGAGGTCTTGCTATGTTGCCCAGGCTGGCCTTGAACTCCTGGCCT GTTTGTACAGATTGGGGCAGGGAGGTCTTGCTGTGTTGCCCAGGCTGGCCTTGAACTCCTGGCCT A G SAE1 Ensembl:ENSG00000142230 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs906902462 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17568136 RMVar_hsa_circ_44245,RMVar_hsa_circ_337323,RMVar_hsa_circ_56834,RMVar_hsa_circ_195562,RMVar_hsa_circ_336917,RMVar_hsa_circ_347680,RMVar_hsa_circ_118551 14895 RMVar_ID_14895 Human_SNP_ID_667685844 A-to-I Human chr19 + 47178537 47178537 47178537 AGCTTTGTTGCCCAGGCTGGAGTTGCAGGTGCAATCTCAGCTCATTGCAACCTCCGCCTTTTGGA AGCTTTGTTGCCCAGGCTGGAGTTGCAGGTGCCATCTCAGCTCATTGCAACCTCCGCCTTTTGGA A C SAE1 Ensembl:ENSG00000142230 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1047831175 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44245,RMVar_hsa_circ_337323,RMVar_hsa_circ_56834,RMVar_hsa_circ_195562,RMVar_hsa_circ_336917,RMVar_hsa_circ_347680,RMVar_hsa_circ_118551 14896 RMVar_ID_14896 Human_SNP_ID_667685845 A-to-I Human chr19 + 47178537 47178537 47178537 AGCTTTGTTGCCCAGGCTGGAGTTGCAGGTGCAATCTCAGCTCATTGCAACCTCCGCCTTTTGGA AGCTTTGTTGCCCAGGCTGGAGTTGCAGGTGCGATCTCAGCTCATTGCAACCTCCGCCTTTTGGA A G SAE1 Ensembl:ENSG00000142230 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1047831175 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44245,RMVar_hsa_circ_337323,RMVar_hsa_circ_56834,RMVar_hsa_circ_195562,RMVar_hsa_circ_336917,RMVar_hsa_circ_347680,RMVar_hsa_circ_118551 14897 RMVar_ID_14897 Human_SNP_ID_667686162 A-to-I Human chr19 + 47179625 47179625 47179625 TGGAGTGCAGTGTCACGATCATAACTTACTGCAGCTTCTCCCTCCCAGCTCAAGCAATCCTCACA TGGAGTGCAGTGTCACGATCATAACTTACTGCGGCTTCTCCCTCCCAGCTCAAGCAATCCTCACA A G SAE1 Ensembl:ENSG00000142230 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1429824853 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44245,RMVar_hsa_circ_337323,RMVar_hsa_circ_56834,RMVar_hsa_circ_195562,RMVar_hsa_circ_336917,RMVar_hsa_circ_347680,RMVar_hsa_circ_118551 14898 RMVar_ID_14898 Human_SNP_ID_667686191 A-to-I Human chr19 + 47179779 47179779 47179779 TAGAGACGGGGTTTCACTGTGTTGCCCAGGGTAGTCTCTGTCTCCTGGGCTGAAGTGAGCCTCCT TAGAGACGGGGTTTCACTGTGTTGCCCAGGGTGGTCTCTGTCTCCTGGGCTGAAGTGAGCCTCCT A G SAE1 Ensembl:ENSG00000142230 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs935949179 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17568138 RMVar_hsa_circ_44245,RMVar_hsa_circ_337323,RMVar_hsa_circ_56834,RMVar_hsa_circ_195562,RMVar_hsa_circ_336917,RMVar_hsa_circ_347680,RMVar_hsa_circ_118551 14899 RMVar_ID_14899 Human_SNP_ID_667686449 A-to-I Human chr19 + 47180712 47180712 47180712 AGATACAGTGGTGCATGCATGTAGTCCTAGCTACTCAGGAGGATGAGATGGGAGGATCGGTTGAG AGATACAGTGGTGCATGCATGTAGTCCTAGCTCCTCAGGAGGATGAGATGGGAGGATCGGTTGAG A C SAE1 Ensembl:ENSG00000142230 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs973826185 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21979999 RMVar_hsa_circ_44245,RMVar_hsa_circ_195562,RMVar_hsa_circ_347680,RMVar_hsa_circ_118551,RMVar_hsa_circ_296637 14900 RMVar_ID_14900 Human_SNP_ID_667686450 A-to-I Human chr19 + 47180712 47180712 47180712 AGATACAGTGGTGCATGCATGTAGTCCTAGCTACTCAGGAGGATGAGATGGGAGGATCGGTTGAG AGATACAGTGGTGCATGCATGTAGTCCTAGCTTCTCAGGAGGATGAGATGGGAGGATCGGTTGAG A T SAE1 Ensembl:ENSG00000142230 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs973826185 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21979999 RMVar_hsa_circ_44245,RMVar_hsa_circ_195562,RMVar_hsa_circ_347680,RMVar_hsa_circ_118551,RMVar_hsa_circ_296637 14901 RMVar_ID_14901 Human_SNP_ID_667688419 A-to-I Human chr19 + 47187705 47187704 47187706 CACAACACCCGGCTCATTTTTGTGTTTTTAGCAGAGACGGGGTTTCACCATGTTGGCCAGGCTGG CACAACACCCGGCTCATTTTTGTGTTTTTAGC__AGACGGGGTTTCACCATGTTGGCCAGGCTGG CAG C SAE1 Ensembl:ENSG00000142230 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1007827278 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_44245,RMVar_hsa_circ_195562,RMVar_hsa_circ_347680,RMVar_hsa_circ_118551,RMVar_hsa_circ_296637 14902 RMVar_ID_14902 Human_SNP_ID_667689295 A-to-I Human chr19 + 47191155 47191155 47191155 TGGGTAGGTTGGGCGTAGTGGGTCATGCCTATAATCCCAGCACTTTGGGAGGCTGAGGCAGGAGG TGGGTAGGTTGGGCGTAGTGGGTCATGCCTATTATCCCAGCACTTTGGGAGGCTGAGGCAGGAGG A T SAE1 Ensembl:ENSG00000142230 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs932524640 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44245,RMVar_hsa_circ_195562,RMVar_hsa_circ_347680,RMVar_hsa_circ_118551,RMVar_hsa_circ_296637 14903 RMVar_ID_14903 Human_SNP_ID_667699173 A-to-I Human chr19 - 47225521 47225521 47225521 AGATCCCCGTTGCTACAAAAAATACAAAAATTAGCCGGGTGTGGTGGCGCGGGCCTGTAGTCTCA AGATCCCCGTTGCTACAAAAAATACAAAAATTGGCCGGGTGTGGTGGCGCGGGCCTGTAGTCTCA T C BBC3 Ensembl:ENSG00000105327 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs990333885 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91604,RMVar_hsa_circ_127412,RMVar_hsa_circ_111052,RMVar_hsa_circ_195569,RMVar_hsa_circ_195570,RMVar_hsa_circ_195568 14904 RMVar_ID_14904 Human_SNP_ID_667710964 A-to-I Human chr19 + 47262921 47262921 47262921 CAGGCTGGGCAACAGAGTGAGACCCCATCTCTATAAAAATTTTAAAAATTAACTGGACGTGGTGG CAGGCTGGGCAACAGAGTGAGACCCCATCTCTGTAAAAATTTTAAAAATTAACTGGACGTGGTGG A G CCDC9 Ensembl:ENSG00000105321 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1049576837 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80689,RMVar_hsa_circ_195572 14905 RMVar_ID_14905 Human_SNP_ID_667713378 A-to-I Human chr19 + 47270243 47270243 47270243 TGTCTGCCTCGGCCTCCCAGAGTGCGGGGATTACAGGCTTGAGCCACCATGCCCGGCCCTGTCCT TGTCTGCCTCGGCCTCCCAGAGTGCGGGGATTGCAGGCTTGAGCCACCATGCCCGGCCCTGTCCT A G CCDC9 Ensembl:ENSG00000105321 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1026378883 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76127,RMVar_hsa_circ_195574 14906 RMVar_ID_14906 Human_SNP_ID_667721240 A-to-I Human chr19 + 47292379 47292379 47292379 GATCTCCTGGACTCAAGCAATCCTCCCACCTCAGCCTCCCCAGTAGTTGGTACTACAGGTGTGCA GATCTCCTGGACTCAAGCAATCCTCCCACCTCGGCCTCCCCAGTAGTTGGTACTACAGGTGTGCA A G C5AR1 Ensembl:ENSG00000197405 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031374543 Functional Loss SNV dbSNP153 33..33 33 - - - 14907 RMVar_ID_14907 Human_SNP_ID_667721460 A-to-I Human chr19 + 47293221 47293221 47293221 TCGGCTCACTGCAACCTCTGGCTCCTGGGTTCAGGCAATTCTCCTGTCTCAGTCTCCTGAGTAGC TCGGCTCACTGCAACCTCTGGCTCCTGGGTTCCGGCAATTCTCCTGTCTCAGTCTCCTGAGTAGC A C C5AR1 Ensembl:ENSG00000197405 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1158737824 Functional Loss SNV dbSNP153 33..33 33 - - - 14908 RMVar_ID_14908 Human_SNP_ID_667721625 A-to-I Human chr19 + 47293823 47293823 47293823 GGCTGAATCCCAGCCACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACCTGGGAGGCGGAAGTT GGCTGAATCCCAGCCACTCAGGAGGCTGAGGCGGGAGAATCGCTTGAACCTGGGAGGCGGAAGTT A G C5AR1 Ensembl:ENSG00000197405 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1022901779 Functional Loss SNV dbSNP153 33..33 33 - - - 14909 RMVar_ID_14909 Human_SNP_ID_667721915 A-to-I Human chr19 + 47294844 47294844 47294844 TTTTTGAGAGATGGGATCTCACTATGTTGCCCAGACTGATCATGAACTCCTGGCCTCAGGCATTC TTTTTGAGAGATGGGATCTCACTATGTTGCCCGGACTGATCATGAACTCCTGGCCTCAGGCATTC A G C5AR1 Ensembl:ENSG00000197405 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs776762251 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13485587 14910 RMVar_ID_14910 Human_SNP_ID_667721924 A-to-I Human chr19 + 47294882 47294882 47294882 ATCATGAACTCCTGGCCTCAGGCATTCCTCCTATCTTGGCCTCCCAAAGTGCTGGGATCACAGGC ATCATGAACTCCTGGCCTCAGGCATTCCTCCTGTCTTGGCCTCCCAAAGTGCTGGGATCACAGGC A G C5AR1 Ensembl:ENSG00000197405 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1319016459 Functional Loss SNV dbSNP153 33..33 33 - - - 14911 RMVar_ID_14911 Human_SNP_ID_667722048 A-to-I Human chr19 + 47295309 47295309 47295309 GTTGGTCAGGCTGGTCTCGAGCTCCTGGCCTCAGGTGATCTGCCTGCCTTGGCCTCCCAAAGTGC GTTGGTCAGGCTGGTCTCGAGCTCCTGGCCTCGGGTGATCTGCCTGCCTTGGCCTCCCAAAGTGC A G C5AR1 Ensembl:ENSG00000197405 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1030931588 Functional Loss SNV dbSNP153 33..33 33 - - - 14912 RMVar_ID_14912 Human_SNP_ID_667722049 A-to-I Human chr19 + 47295309 47295309 47295309 GTTGGTCAGGCTGGTCTCGAGCTCCTGGCCTCAGGTGATCTGCCTGCCTTGGCCTCCCAAAGTGC GTTGGTCAGGCTGGTCTCGAGCTCCTGGCCTCTGGTGATCTGCCTGCCTTGGCCTCCCAAAGTGC A T C5AR1 Ensembl:ENSG00000197405 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1030931588 Functional Loss SNV dbSNP153 33..33 33 - - - 14913 RMVar_ID_14913 Human_SNP_ID_667737931 A-to-I Human chr19 + 47350521 47350521 47350521 TTGGCTCACTGCAACCTCTGCCTCCTGGGTTCAAGCGAGTCTCCTGCCTCAGCCTCCAGAGTAGC TTGGCTCACTGCAACCTCTGCCTCCTGGGTTCCAGCGAGTCTCCTGCCTCAGCCTCCAGAGTAGC A C DHX34 Ensembl:ENSG00000134815 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs941507801 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106316,RMVar_hsa_circ_195576 14914 RMVar_ID_14914 Human_SNP_ID_667737981 A-to-I Human chr19 + 47350680 47350680 47350680 GACCTCAGGTGATCTGCCTGCCTCAGCCTCCCAAAGTGCTGGGATTATAGGCGTGAGCCACCATG GACCTCAGGTGATCTGCCTGCCTCAGCCTCCCGAAGTGCTGGGATTATAGGCGTGAGCCACCATG A G DHX34 Ensembl:ENSG00000134815 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1487896904 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106316,RMVar_hsa_circ_195576 14915 RMVar_ID_14915 Human_SNP_ID_667738494 A-to-I Human chr19 + 47352528 47352528 47352528 TGAGATCTCATCTCTACAAACAGTAAAAAATTAGCTGGGTGTGGTGGCATGTGCCTGTAGTCCCA TGAGATCTCATCTCTACAAACAGTAAAAAATTGGCTGGGTGTGGTGGCATGTGCCTGTAGTCCCA A G DHX34 Ensembl:ENSG00000134815 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1208420123 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_138205 RMVar_hsa_circ_106316,RMVar_hsa_circ_195576 14916 RMVar_ID_14916 Human_SNP_ID_667738524 A-to-I Human chr19 + 47352657 47352657 47352657 TGATTACGGCACTGCACTCCAGCCTGGGAAACAGAGTGAGACCCTGCCTCAAAAAGAAAAAAACA TGATTACGGCACTGCACTCCAGCCTGGGAAACCGAGTGAGACCCTGCCTCAAAAAGAAAAAAACA A C DHX34 Ensembl:ENSG00000134815 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1274393307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_138205,Human_RBP_ID_22974793 RMVar_hsa_circ_106316,RMVar_hsa_circ_195576 14917 RMVar_ID_14917 Human_SNP_ID_667741623 A-to-I Human chr19 + 47362883 47362883 47362883 GCCTCCATATTACAGGCTCAAATGATCCTCCTACCTCCACCTGCCAAGTAGCTGGGACCACAGGC GCCTCCATATTACAGGCTCAAATGATCCTCCTGCCTCCACCTGCCAAGTAGCTGGGACCACAGGC A G DHX34 Ensembl:ENSG00000134815 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs901386232 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84184,RMVar_hsa_circ_106316,RMVar_hsa_circ_195576,RMVar_hsa_circ_44181,RMVar_hsa_circ_50528,RMVar_hsa_circ_18540,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_325137,RMVar_hsa_circ_104747 14918 RMVar_ID_14918 Human_SNP_ID_667749104 A-to-I Human chr19 + 47385537 47385537 47385537 CTCCCTGCAACCTCTGCTTCTGGGATTCAAGCAATTCTCCTGCCTCAGCCTTCCGAGTATGTGGG CTCCCTGCAACCTCTGCTTCTGGGATTCAAGCGATTCTCCTGCCTCAGCCTTCCGAGTATGTGGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1203806129 Functional Loss SNV dbSNP153 33..33 33 - - - 14919 RMVar_ID_14919 Human_SNP_ID_667754603 A-to-I Human chr19 - 47404848 47404848 47404848 CCTCAGCCCTGCCCTCATGGGGCACAAAGTCTAGTGAAGGGGACAGACCCATCCCCAGATGGTGA CCTCAGCCCTGCCCTCATGGGGCACAAAGTCTGGTGAAGGGGACAGACCCATCCCCAGATGGTGA T C MEIS3 Ensembl:ENSG00000105419 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1038214770 Functional Loss SNV dbSNP153 33..33 33 - - - 14920 RMVar_ID_14920 Human_SNP_ID_667756068 A-to-I Human chr19 - 47409723 47409723 47409723 GAGTAGCTAGGACTACAGGTGCATGCCACCACACCCGGCTAATTTTTTGTATTTTTAGTAGAGAC GAGTAGCTAGGACTACAGGTGCATGCCACCACGCCCGGCTAATTTTTTGTATTTTTAGTAGAGAC T C MEIS3 Ensembl:ENSG00000105419 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1195185376 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32857 14921 RMVar_ID_14921 Human_SNP_ID_667756074 A-to-I Human chr19 - 47409733 47409733 47409733 TCAGCCTCCTGAGTAGCTAGGACTACAGGTGCATGCCACCACACCCGGCTAATTTTTTGTATTTT TCAGCCTCCTGAGTAGCTAGGACTACAGGTGCCTGCCACCACACCCGGCTAATTTTTTGTATTTT T G MEIS3 Ensembl:ENSG00000105419 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs781299204 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32857 14922 RMVar_ID_14922 Human_SNP_ID_667756075 A-to-I Human chr19 - 47409739 47409738 47409739 CCTGCCTCAGCCTCCTGAGTAGCTAGGACTACAGGTGCATGCCACCACACCCGGCTAATTTTTTG CCTGCCTCAGCCTCCTGAGTAGCTAGGACTAC_GGTGCATGCCACCACACCCGGCTAATTTTTTG CT C MEIS3 Ensembl:ENSG00000105419 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1482291557 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_32857 14923 RMVar_ID_14923 Human_SNP_ID_667756076 A-to-I Human chr19 - 47409747 47409747 47409747 GCGATTCTCCTGCCTCAGCCTCCTGAGTAGCTAGGACTACAGGTGCATGCCACCACACCCGGCTA GCGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGTGCATGCCACCACACCCGGCTA T C MEIS3 Ensembl:ENSG00000105419 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1200438934 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32857 14924 RMVar_ID_14924 Human_SNP_ID_667767674 A-to-I Human chr19 - 47449460 47449460 47449460 AAAATTAGCCAGGCATGGTGGCAGGCGCCTGTAGTCCCAGCTGCTCGGGAGGCTGAGGTGGGAGA AAAATTAGCCAGGCATGGTGGCAGGCGCCTGTGGTCCCAGCTGCTCGGGAGGCTGAGGTGGGAGA T C SLC8A2 Ensembl:ENSG00000118160 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1206746101 Functional Loss SNV dbSNP153 33..33 33 - - - 14925 RMVar_ID_14925 Human_SNP_ID_667776878 A-to-I Human chr19 - 47482407 47482407 47482407 CTCGATCTCTGCAACCTCTACCTCCCTGGTTCAAGTGATTCTACTGCCTCAGCCTCCTGAGTAGC CTCGATCTCTGCAACCTCTACCTCCCTGGTTCGAGTGATTCTACTGCCTCAGCCTCCTGAGTAGC T C KPTN Ensembl:ENSG00000118162 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893356785 Functional Loss SNV dbSNP153 33..33 33 - - - 14926 RMVar_ID_14926 Human_SNP_ID_667812127 A-to-I Human chr19 + 47612224 47612224 47612224 ATTGCTTGAGCCCTGGATTTTAAGACCAGCCTAGGCAACACGGTGAGACCCTGTGTCTACAAAAA ATTGCTTGAGCCCTGGATTTTAAGACCAGCCTGGGCAACACGGTGAGACCCTGTGTCTACAAAAA A G AC010519.1,BICRA Ensembl:ENSG00000268746,Ensembl:ENSG00000063169 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs541909108 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17568142 14927 RMVar_ID_14927 Human_SNP_ID_667812163 A-to-I Human chr19 + 47612395 47612395 47612395 CCGTGATTGTGCCACTGCTCTCAAGCCTGGGCAAGAGTGAGACCCTGTCTCAAAAAAAAAAAATA CCGTGATTGTGCCACTGCTCTCAAGCCTGGGCCAGAGTGAGACCCTGTCTCAAAAAAAAAAAATA A C AC010519.1,BICRA Ensembl:ENSG00000268746,Ensembl:ENSG00000063169 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1464933471 Functional Loss SNV dbSNP153 33..33 33 - - - 14928 RMVar_ID_14928 Human_SNP_ID_667812743 A-to-I Human chr19 + 47614496 47614496 47614496 AAAATGAGCTGGGCATGGTGGTGCATGGCTGTAATCCCAGCTACTCAGGAGCCTGAGGCAGGGGA AAAATGAGCTGGGCATGGTGGTGCATGGCTGTGATCCCAGCTACTCAGGAGCCTGAGGCAGGGGA A G AC010519.1,BICRA Ensembl:ENSG00000268746,Ensembl:ENSG00000063169 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1218723027 Functional Loss SNV dbSNP153 33..33 33 - - - 14929 RMVar_ID_14929 Human_SNP_ID_667813494 A-to-I Human chr19 + 47617178 47617178 47617178 TATTTTATTTTATAGAGACAAGGTCTTGCTATATTGCTCAGGCTGGTCTCCAACTTCTGGGCTCA TATTTTATTTTATAGAGACAAGGTCTTGCTATGTTGCTCAGGCTGGTCTCCAACTTCTGGGCTCA A G AC010519.1,BICRA Ensembl:ENSG00000268746,Ensembl:ENSG00000063169 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1461643791 Functional Loss SNV dbSNP153 33..33 33 - - - 14930 RMVar_ID_14930 Human_SNP_ID_667819854 A-to-I Human chr19 + 47640307 47640306 47640307 TCATCCCAGCACATTGGGAGGCTGAGGCAGGCAGATCACTTGAGGACAGGAGTTCGAGACCGGCC TCATCCCAGCACATTGGGAGGCTGAGGCAGGC_GATCACTTGAGGACAGGAGTTCGAGACCGGCC CA C AC010519.1,BICRA Ensembl:ENSG00000268746,Ensembl:ENSG00000063169 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1224708575 Functional Loss DEL dbSNP153 33..33 33 - - - 14931 RMVar_ID_14931 Human_SNP_ID_667820067 A-to-I Human chr19 + 47641040 47641040 47641040 TCCTACCTCAGCCTCCTGAGTAAGCTGGGACTACAGGCACCCACCACCACCATGCCTGGCTAATT TCCTACCTCAGCCTCCTGAGTAAGCTGGGACTGCAGGCACCCACCACCACCATGCCTGGCTAATT A G AC010519.1,BICRA Ensembl:ENSG00000268746,Ensembl:ENSG00000063169 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs573728708 Functional Loss SNV dbSNP153 33..33 33 - - - 14932 RMVar_ID_14932 Human_SNP_ID_667820423 A-to-I Human chr19 + 47642439 47642439 47642439 TAGAAACTGCCCACCTGGGCGCAGTGGCTCACACCTGTAGTCCCAGCACTTTGGGAGACTGAGGC TAGAAACTGCCCACCTGGGCGCAGTGGCTCACCCCTGTAGTCCCAGCACTTTGGGAGACTGAGGC A C AC010519.1,BICRA Ensembl:ENSG00000268746,Ensembl:ENSG00000063169 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1360680589 Functional Loss SNV dbSNP153 33..33 33 - - - 14933 RMVar_ID_14933 Human_SNP_ID_667820586 A-to-I Human chr19 + 47643170 47643170 47643170 TTTTGTATTTTTTGTAAAGACAAGGTTTCGCCATGTTGGCCGAGCTGGTCTTGAACTCCTGACCT TTTTGTATTTTTTGTAAAGACAAGGTTTCGCCGTGTTGGCCGAGCTGGTCTTGAACTCCTGACCT A G AC010519.1,BICRA Ensembl:ENSG00000268746,Ensembl:ENSG00000063169 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1205463101 Functional Loss SNV dbSNP153 33..33 33 - - - 14934 RMVar_ID_14934 Human_SNP_ID_667820829 A-to-I Human chr19 + 47644152 47644152 47644152 GGGATCCTTCCACCTCAGTCTCCCAAGTGGCTAGGACTACAGGTGTGCCCATGATGCCCAGCTAA GGGATCCTTCCACCTCAGTCTCCCAAGTGGCTGGGACTACAGGTGTGCCCATGATGCCCAGCTAA A G AC010519.1,BICRA Ensembl:ENSG00000268746,Ensembl:ENSG00000063169 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1222193334 Functional Loss SNV dbSNP153 33..33 33 - - - 14935 RMVar_ID_14935 Human_SNP_ID_667824320 A-to-I Human chr19 + 47656880 47656880 47656880 TGGATATTGTAGATTTGTTTGGTTTTTTTTTTAAGATGGAGTCTTGCTCTGTCGCCCAGGCTGGA TGGATATTGTAGATTTGTTTGGTTTTTTTTTTGAGATGGAGTCTTGCTCTGTCGCCCAGGCTGGA A G AC010519.1,BICRA Ensembl:ENSG00000268746,Ensembl:ENSG00000063169 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs915858438 Functional Loss SNV dbSNP153 33..33 33 - - - 14936 RMVar_ID_14936 Human_SNP_ID_667832565 A-to-I Human chr19 + 47685069 47685069 47685069 ATTGACTCCTACAACCTCCGCCTCCCATGCTTAAGTGATCCTCCCACCTCAGCCTCCGAAGTAGC ATTGACTCCTACAACCTCCGCCTCCCATGCTTCAGTGATCCTCCCACCTCAGCCTCCGAAGTAGC A C AC010519.1,BICRA Ensembl:ENSG00000268746,Ensembl:ENSG00000063169 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1456035062 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_357794 14937 RMVar_ID_14937 Human_SNP_ID_667833501 A-to-I Human chr19 + 47687785 47687785 47687785 AGAGGGTTGCAGTGAGCTGAGATCGTGCCACTACACTCTAGCCTAGGCAGCAGAGTGAGACTCTG AGAGGGTTGCAGTGAGCTGAGATCGTGCCACTGCACTCTAGCCTAGGCAGCAGAGTGAGACTCTG A G AC010519.1,BICRA Ensembl:ENSG00000268746,Ensembl:ENSG00000063169 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1241264442 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25428031 RMVar_hsa_circ_357794 14938 RMVar_ID_14938 Human_SNP_ID_667844041 A-to-I Human chr19 + 47721588 47721588 47721588 CACCCACCTCGGCCTCCCAAAGTGTTGGGATTACAGGCATGAGCCACCGCCCAGCCTATTTTCTG CACCCACCTCGGCCTCCCAAAGTGTTGGGATTTCAGGCATGAGCCACCGCCCAGCCTATTTTCTG A T EHD2,AC010519.1 Ensembl:ENSG00000024422,Ensembl:ENSG00000268746 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs950913643 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123772,RMVar_hsa_circ_120086,RMVar_hsa_circ_266961,RMVar_hsa_circ_195609,RMVar_hsa_circ_345635,RMVar_hsa_circ_271893,RMVar_hsa_circ_195612,RMVar_hsa_circ_195614,RMVar_hsa_circ_195613 14939 RMVar_ID_14939 Human_SNP_ID_667847178 A-to-I Human chr19 + 47732153 47732153 47732153 TTTATTATTATTTTGTTTTGAGACTGAGTCTCACTCTGTCGCCCAGGCTGGTGCAATGGCACGGT TTTATTATTATTTTGTTTTGAGACTGAGTCTCGCTCTGTCGCCCAGGCTGGTGCAATGGCACGGT A G EHD2,AC010519.1 Ensembl:ENSG00000024422,Ensembl:ENSG00000268746 Protein coding,lincRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1488920832 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13488596 Human_Splice_Rec_2024498,Human_Splice_Rec_2024499 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 14940 RMVar_ID_14940 Human_SNP_ID_667850711 A-to-I Human chr19 + 47744157 47744157 47744157 CTCCCACCTCAGCCTCCCGAGTACCTGGGACTACAGGCGCACACCATCACGCCTGGCTAATTTTT CTCCCACCTCAGCCTCCCGAGTACCTGGGACTGCAGGCGCACACCATCACGCCTGGCTAATTTTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1267476123 Functional Loss SNV dbSNP153 33..33 33 - - - 14941 RMVar_ID_14941 Human_SNP_ID_667852843 A-to-I Human chr19 - 47750220 47750220 47750220 GGATGAGGTCAACCCGAAGGGGTTTCTTGAGAAGCAGTGACTTCTTCTGGACTTTGGTTCTCTTC GGATGAGGTCAACCCGAAGGGGTTTCTTGAGAGGCAGTGACTTCTTCTGGACTTTGGTTCTCTTC T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs746705150 Functional Loss SNV dbSNP153 33..33 33 - - - 14942 RMVar_ID_14942 Human_SNP_ID_667856174 A-to-I Human chr19 + 47759092 47759092 47759092 GCTGCCCAGGCTGGCCTCAAACTCCTGACCTCAAGCGATCCACCCACCTTGGCTTCCCAAAGTGC GCTGCCCAGGCTGGCCTCAAACTCCTGACCTCGAGCGATCCACCCACCTTGGCTTCCCAAAGTGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs915647765 Functional Loss SNV dbSNP153 33..33 33 - - - 14943 RMVar_ID_14943 Human_SNP_ID_667859940 A-to-I Human chr19 + 47771597 47771597 47771597 GGGAGGCTGAGTTGGAAGGATCACCTGAGCCCAGGAGGTCGAGGTTGCAGTGAGCCATGATCATG GGGAGGCTGAGTTGGAAGGATCACCTGAGCCCCGGAGGTCGAGGTTGCAGTGAGCCATGATCATG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1294564048 Functional Loss SNV dbSNP153 33..33 33 - - - 14944 RMVar_ID_14944 Human_SNP_ID_667938746 A-to-I Human chr19 - 48068453 48068453 48068453 GTCTCAAACTTCTGGGCTCAAGCAATCCTCCCACCTCGGCTTCCCTAAGTCCTGGGATTACTCTG GTCTCAAACTTCTGGGCTCAAGCAATCCTCCCGCCTCGGCTTCCCTAAGTCCTGGGATTACTCTG T C PLA2G4C Ensembl:ENSG00000105499 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1274835068 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_195632,RMVar_hsa_circ_195629,RMVar_hsa_circ_368767 14945 RMVar_ID_14945 Human_SNP_ID_667938747 A-to-I Human chr19 - 48068453 48068453 48068453 GTCTCAAACTTCTGGGCTCAAGCAATCCTCCCACCTCGGCTTCCCTAAGTCCTGGGATTACTCTG GTCTCAAACTTCTGGGCTCAAGCAATCCTCCCCCCTCGGCTTCCCTAAGTCCTGGGATTACTCTG T G PLA2G4C Ensembl:ENSG00000105499 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1274835068 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_195632,RMVar_hsa_circ_195629,RMVar_hsa_circ_368767 14946 RMVar_ID_14946 Human_SNP_ID_667938763 A-to-I Human chr19 - 48068517 48068517 48068517 CAGCTAATTTGTTTATTTTATTTTATTTTTGTAAAGATGTGGTCTCGCTCTCTTGCCCAAGCTGG CAGCTAATTTGTTTATTTTATTTTATTTTTGTGAAGATGTGGTCTCGCTCTCTTGCCCAAGCTGG T C PLA2G4C Ensembl:ENSG00000105499 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1351151149 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_195632,RMVar_hsa_circ_195629,RMVar_hsa_circ_368767 14947 RMVar_ID_14947 Human_SNP_ID_667938775 A-to-I Human chr19 - 48068573 48068573 48068573 ATCCTCCTGCCTCAGCCTTCTGAATAGCTGGGACCACAGGCATGCATTAATATGCCCAGCTAATT ATCCTCCTGCCTCAGCCTTCTGAATAGCTGGGGCCACAGGCATGCATTAATATGCCCAGCTAATT T C PLA2G4C Ensembl:ENSG00000105499 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1476393672 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_195632,RMVar_hsa_circ_195629,RMVar_hsa_circ_368767 14948 RMVar_ID_14948 Human_SNP_ID_667938776 A-to-I Human chr19 - 48068582 48068582 48068582 GTTCAAGTGATCCTCCTGCCTCAGCCTTCTGAATAGCTGGGACCACAGGCATGCATTAATATGCC GTTCAAGTGATCCTCCTGCCTCAGCCTTCTGAGTAGCTGGGACCACAGGCATGCATTAATATGCC T C PLA2G4C Ensembl:ENSG00000105499 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1020774749 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_195632,RMVar_hsa_circ_195629,RMVar_hsa_circ_368767 14949 RMVar_ID_14949 Human_SNP_ID_667939535 A-to-I Human chr19 - 48071708 48071708 48071708 GTGATGGCTCACGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCGGGAGGGTCGCTTGAGGCCA GTGATGGCTCACGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCGGGAGGGTCGCTTGAGGCCA T C PLA2G4C Ensembl:ENSG00000105499 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs953688799 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_195632,RMVar_hsa_circ_195629,RMVar_hsa_circ_368767 14950 RMVar_ID_14950 Human_SNP_ID_667939836 A-to-I Human chr19 - 48073186 48073186 48073186 AAAAAATTAGCTGGACATGGTAGTGCGTTCCCATGGTCCCAGCTACTCAGGAGGCTGAGGCAGGA AAAAAATTAGCTGGACATGGTAGTGCGTTCCCGTGGTCCCAGCTACTCAGGAGGCTGAGGCAGGA T C PLA2G4C Ensembl:ENSG00000105499 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1253525739 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_195632,RMVar_hsa_circ_195629,RMVar_hsa_circ_368767 14951 RMVar_ID_14951 Human_SNP_ID_667941909 A-to-I Human chr19 - 48082043 48082043 48082043 ACAGTCTCACTCTGTTGCCCAGGCTGGAGTGCAGTAGCAAGATCTCGTCTCACTGCAACCTCTGT ACAGTCTCACTCTGTTGCCCAGGCTGGAGTGCGGTAGCAAGATCTCGTCTCACTGCAACCTCTGT T C PLA2G4C Ensembl:ENSG00000105499 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1186768425 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110578,RMVar_hsa_circ_68877,RMVar_hsa_circ_195630,RMVar_hsa_circ_87030,RMVar_hsa_circ_195631 14952 RMVar_ID_14952 Human_SNP_ID_667945650 A-to-I Human chr19 - 48097079 48097079 48097079 ACGATCTCGGCTCACCACAACCTCCGCCTCCCAGGTTCAAGCGATTCTCCTGCCCCAGCCTCCCG ACGATCTCGGCTCACCACAACCTCCGCCTCCCGGGTTCAAGCGATTCTCCTGCCCCAGCCTCCCG T C PLA2G4C Ensembl:ENSG00000105499 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1178828370 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2025114,Human_Splice_Rec_2025120 RMVar_hsa_circ_87030,RMVar_hsa_circ_195631,RMVar_hsa_circ_35293,RMVar_hsa_circ_195633,RMVar_hsa_circ_76847,RMVar_hsa_circ_54575,RMVar_hsa_circ_267201,RMVar_hsa_circ_195634 14953 RMVar_ID_14953 Human_SNP_ID_667949217 A-to-I Human chr19 - 48108226 48108226 48108226 GGAGGCCAAGGCAGGAGGATTGCTTGAGCCCAAGAGTTGGAGGCTGCAGTGAGCTATGATTGCGC GGAGGCCAAGGCAGGAGGATTGCTTGAGCCCAGGAGTTGGAGGCTGCAGTGAGCTATGATTGCGC T C PLA2G4C Ensembl:ENSG00000105499 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1478204357 Functional Loss SNV dbSNP153 33..33 33 - - - 14954 RMVar_ID_14954 Human_SNP_ID_667953670 A-to-I Human chr19 - 48123218 48123218 48123218 CGAGTTTGTCTTCGCCACCTCCCTGGACACCAAGGACATCGAGCAGATCGCCGAGTTCCTGGAGC CGAGTTTGTCTTCGCCACCTCCCTGGACACCAGGGACATCGAGCAGATCGCCGAGTTCCTGGAGC T C LIG1 Ensembl:ENSG00000105486 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs780941248 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1890648,Human_RBP_ID_3955302,Human_RBP_ID_17935464,Human_RBP_ID_26338055 Human_Splice_Rec_2025217,Human_Splice_Rec_2025267,Human_Splice_Rec_2025323,Human_Splice_Rec_2025373,Human_Splice_Rec_2025417,Human_Splice_Rec_2025469,Human_Splice_Rec_2025521,Human_Splice_Rec_2025543,Human_Splice_Rec_2025547 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 14955 RMVar_ID_14955 Human_SNP_ID_667954378 A-to-I Human chr19 - 48125796 48125796 48125796 TTTAGTAGAGACGGTGTTTCACCATGTTGGCCAGGATGGTCTTGATCTCCTGACATCGTGATCTG TTTAGTAGAGACGGTGTTTCACCATGTTGGCCGGGATGGTCTTGATCTCCTGACATCGTGATCTG T C LIG1 Ensembl:ENSG00000105486 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1179842320 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33777,RMVar_hsa_circ_98837,RMVar_hsa_circ_108565,RMVar_hsa_circ_195636,RMVar_hsa_circ_69641,RMVar_hsa_circ_195637,RMVar_hsa_circ_195639,RMVar_hsa_circ_6330,RMVar_hsa_circ_124141,RMVar_hsa_circ_195638 14956 RMVar_ID_14956 Human_SNP_ID_667957009 A-to-I Human chr19 - 48135239 48135239 48135239 TACTTGGGAAACTGAGGCACAAGAATCATTTGAACCCAGGAGTTGGAGGCTGCAGTGAGCTGAGA TACTTGGGAAACTGAGGCACAAGAATCATTTGGACCCAGGAGTTGGAGGCTGCAGTGAGCTGAGA T C LIG1 Ensembl:ENSG00000105486 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1424107531 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13489568 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 14957 RMVar_ID_14957 Human_SNP_ID_667959394 A-to-I Human chr19 - 48142931 48142931 48142931 TTTATATAAATATTATCATGGAGGCTGGGTGCAGTGGCTCATGCCTTAATTCCAGCACATCGGGA TTTATATAAATATTATCATGGAGGCTGGGTGCGGTGGCTCATGCCTTAATTCCAGCACATCGGGA T C LIG1 Ensembl:ENSG00000105486 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1301004527 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5443312 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_34463,RMVar_hsa_circ_99647,RMVar_hsa_circ_195653 14958 RMVar_ID_14958 Human_SNP_ID_667960351 A-to-I Human chr19 - 48146300 48146300 48146300 TTTAATTTCTCCATGTTGGCCAGGTTGGTCTCAAACTCCCGACCTCAGTGATCTGCCTGCCTCGG TTTAATTTCTCCATGTTGGCCAGGTTGGTCTCGAACTCCCGACCTCAGTGATCTGCCTGCCTCGG T C LIG1 Ensembl:ENSG00000105486 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1169059379 Functional Loss SNV dbSNP153 33..33 33 - - - 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_48843,RMVar_hsa_circ_34463,RMVar_hsa_circ_99647,RMVar_hsa_circ_195653,RMVar_hsa_circ_83444,RMVar_hsa_circ_195654 14959 RMVar_ID_14959 Human_SNP_ID_667962080 A-to-I Human chr19 - 48152360 48152360 48152360 CCAGCAGTTTGGGAGGCCGAAGCGGGTGGATCACTTGAGGTCGGGAGTTGGAGACCAGCCTGGCC CCAGCAGTTTGGGAGGCCGAAGCGGGTGGATCCCTTGAGGTCGGGAGTTGGAGACCAGCCTGGCC T G LIG1 Ensembl:ENSG00000105486 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs767392664 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112967,RMVar_hsa_circ_124141,RMVar_hsa_circ_195638,RMVar_hsa_circ_95771,RMVar_hsa_circ_86212,RMVar_hsa_circ_121148,RMVar_hsa_circ_195642,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 14960 RMVar_ID_14960 Human_SNP_ID_667962216 A-to-I Human chr19 - 48152978 48152978 48152978 TGACCAAGCTGGTCTCGAACTCCTGAGCTCACATGATCTGCCCACCTCGGCCTCACAAAGCCCTG TGACCAAGCTGGTCTCGAACTCCTGAGCTCACGTGATCTGCCCACCTCGGCCTCACAAAGCCCTG T C LIG1 Ensembl:ENSG00000105486 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs547656937 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13489995,Human_RBP_ID_25428357 RMVar_hsa_circ_112967,RMVar_hsa_circ_124141,RMVar_hsa_circ_195638,RMVar_hsa_circ_95771,RMVar_hsa_circ_86212,RMVar_hsa_circ_121148,RMVar_hsa_circ_195642,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 14961 RMVar_ID_14961 Human_SNP_ID_667962235 A-to-I Human chr19 - 48153073 48153073 48153073 CTCCCACCTCAGCTTCCCGAGTAGCTGGGATTACAGACACACCACCACGCCCAGCTAATTTTTGT CTCCCACCTCAGCTTCCCGAGTAGCTGGGATTGCAGACACACCACCACGCCCAGCTAATTTTTGT T C LIG1 Ensembl:ENSG00000105486 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1182055391 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112967,RMVar_hsa_circ_124141,RMVar_hsa_circ_195638,RMVar_hsa_circ_95771,RMVar_hsa_circ_86212,RMVar_hsa_circ_121148,RMVar_hsa_circ_195642,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 14962 RMVar_ID_14962 Human_SNP_ID_667971270 A-to-I Human chr19 + 48185687 48185687 48185687 CAGCACTGCCCGGTGGAACTTTCTACAATGATAGAAATGTTCCTTATCCAGGCTAGGCATGGTTA CAGCACTGCCCGGTGGAACTTTCTACAATGATGGAAATGTTCCTTATCCAGGCTAGGCATGGTTA A G ZSWIM9 Ensembl:ENSG00000185453 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1228480542 Functional Loss SNV dbSNP153 33..33 33 - - - 14963 RMVar_ID_14963 Human_SNP_ID_667971321 A-to-I Human chr19 + 48185961 48185961 48185961 TGAGCTGAGATTATGCCACTGTACTCTGGCCTAGGTAACAGAGTGACACTCTTGTCTAAAAAAAT TGAGCTGAGATTATGCCACTGTACTCTGGCCTGGGTAACAGAGTGACACTCTTGTCTAAAAAAAT A G ZSWIM9 Ensembl:ENSG00000185453 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946619249 Functional Loss SNV dbSNP153 33..33 33 - - - 14964 RMVar_ID_14964 Human_SNP_ID_667971322 A-to-I Human chr19 + 48185965 48185964 48185965 CTGAGATTATGCCACTGTACTCTGGCCTAGGTAACAGAGTGACACTCTTGTCTAAAAAAATAAAA CTGAGATTATGCCACTGTACTCTGGCCTAGGT_ACAGAGTGACACTCTTGTCTAAAAAAATAAAA TA T ZSWIM9 Ensembl:ENSG00000185453 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1456722393 Functional Loss DEL dbSNP153 33..33 33 - - - 14965 RMVar_ID_14965 Human_SNP_ID_667971323 A-to-I Human chr19 + 48185965 48185965 48185965 CTGAGATTATGCCACTGTACTCTGGCCTAGGTAACAGAGTGACACTCTTGTCTAAAAAAATAAAA CTGAGATTATGCCACTGTACTCTGGCCTAGGTGACAGAGTGACACTCTTGTCTAAAAAAATAAAA A G ZSWIM9 Ensembl:ENSG00000185453 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs979265543 Functional Loss SNV dbSNP153 33..33 33 - - - 14966 RMVar_ID_14966 Human_SNP_ID_667972340 A-to-I Human chr19 + 48188466 48188466 48188466 GGCCAGAATGGTCTCGATCTCCTGGCCTGGTGATCTGCCTGCCTCGGCCTCCCAAAGTGCTGGGA GGCCAGAATGGTCTCGATCTCCTGGCCTGGTGGTCTGCCTGCCTCGGCCTCCCAAAGTGCTGGGA A G ZSWIM9 Ensembl:ENSG00000185453 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1367488057 Functional Loss SNV dbSNP153 33..33 33 - - - 14967 RMVar_ID_14967 Human_SNP_ID_667977765 A-to-I Human chr19 - 48208009 48208009 48208009 ATAGAAGGCCGGATGCAGTGGCTCACGCCTGTAATCCCAACACTTTGGGAGGCCGAGGTGGGTGA ATAGAAGGCCGGATGCAGTGGCTCACGCCTGTGATCCCAACACTTTGGGAGGCCGAGGTGGGTGA T C CARD8 Ensembl:ENSG00000105483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1490496004 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_195661 14968 RMVar_ID_14968 Human_SNP_ID_667982128 A-to-I Human chr19 - 48224902 48224902 48224902 AACAATACAAACAATTAGCCGGGCACGGTGGCAGGTGCCTGTAGTCCCAGCTACTCGGGAGGCTG AACAATACAAACAATTAGCCGGGCACGGTGGCGGGTGCCTGTAGTCCCAGCTACTCGGGAGGCTG T C CARD8 Ensembl:ENSG00000105483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1347238777 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_137658 RMVar_hsa_circ_101330,RMVar_hsa_circ_265459,RMVar_hsa_circ_265803,RMVar_hsa_circ_342096,RMVar_hsa_circ_329028,RMVar_hsa_circ_323951,RMVar_hsa_circ_281323,RMVar_hsa_circ_195665,RMVar_hsa_circ_363217,RMVar_hsa_circ_366195,RMVar_hsa_circ_73919,RMVar_hsa_circ_195666 14969 RMVar_ID_14969 Human_SNP_ID_667982666 A-to-I Human chr19 - 48226975 48226975 48226975 AAGTGAAGTGATTCTCATGCCTCACCGGGATTATGGTGTCTGCCACCACGCCCAGCTATTTGTAT AAGTGAAGTGATTCTCATGCCTCACCGGGATTGTGGTGTCTGCCACCACGCCCAGCTATTTGTAT T C CARD8 Ensembl:ENSG00000105483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1414919183 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18736889 RMVar_hsa_circ_101330,RMVar_hsa_circ_265459,RMVar_hsa_circ_265803,RMVar_hsa_circ_342096,RMVar_hsa_circ_329028,RMVar_hsa_circ_323951,RMVar_hsa_circ_281323,RMVar_hsa_circ_195665,RMVar_hsa_circ_363217,RMVar_hsa_circ_366195,RMVar_hsa_circ_73919,RMVar_hsa_circ_195666 14970 RMVar_ID_14970 Human_SNP_ID_667985555 A-to-I Human chr19 - 48237631 48237631 48237631 TACCACACCTGGCTAATTTTTGTATTTTTAGTAGATACGGGGTTTCACCATGTTGGCCAGGCTGG TACCACACCTGGCTAATTTTTGTATTTTTAGTGGATACGGGGTTTCACCATGTTGGCCAGGCTGG T C CARD8 Ensembl:ENSG00000105483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1033394972 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25428568 RMVar_hsa_circ_329028,RMVar_hsa_circ_323951,RMVar_hsa_circ_281323,RMVar_hsa_circ_73919,RMVar_hsa_circ_195666,RMVar_hsa_circ_369929,RMVar_hsa_circ_273947,RMVar_hsa_circ_54768,RMVar_hsa_circ_195668,RMVar_hsa_circ_350448,RMVar_hsa_circ_363541,RMVar_hsa_circ_295416,RMVar_hsa_circ_342679 14971 RMVar_ID_14971 Human_SNP_ID_667985577 A-to-I Human chr19 - 48237737 48237737 48237737 GCTGGAGTGCAGTGGCACGATCTTGGCTCACTACAACCTCTGCTTCTGGGGTTCAAGCGATTCTT GCTGGAGTGCAGTGGCACGATCTTGGCTCACTGCAACCTCTGCTTCTGGGGTTCAAGCGATTCTT T C CARD8 Ensembl:ENSG00000105483 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1444459765 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25428569 RMVar_hsa_circ_329028,RMVar_hsa_circ_323951,RMVar_hsa_circ_281323,RMVar_hsa_circ_73919,RMVar_hsa_circ_195666,RMVar_hsa_circ_369929,RMVar_hsa_circ_273947,RMVar_hsa_circ_54768,RMVar_hsa_circ_195668,RMVar_hsa_circ_350448,RMVar_hsa_circ_363541,RMVar_hsa_circ_295416,RMVar_hsa_circ_342679 14972 RMVar_ID_14972 Human_SNP_ID_667988749 A-to-I Human chr19 - 48249841 48249841 48249841 TAGGAACTTCTCCCTTTCTTCTCAAGTGACCAAGAGGAACAGAACACAGAGCAGCCTGGCAGTGT TAGGAACTTCTCCCTTTCTTCTCAAGTGACCAGGAGGAACAGAACACAGAGCAGCCTGGCAGTGT T C CARD8 Ensembl:ENSG00000105483 Protein coding 5'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1206927533 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_825497 Human_Splice_Rec_2025682,Human_Splice_Rec_2025683,Human_Splice_Rec_2025720,Human_Splice_Rec_2025721,Human_Splice_Rec_2025765,Human_Splice_Rec_2025810,Human_Splice_Rec_2025811,Human_Splice_Rec_2025838,Human_Splice_Rec_2025839,Human_Splice_Rec_2025861,Human_Splice_Rec_2025887,Human_Splice_Rec_2025909,Human_Splice_Rec_2025931,Human_Splice_Rec_2025953,Human_Splice_Rec_2025974,Human_Splice_Rec_2025975,Human_Splice_Rec_2026023,Human_Splice_Rec_2026042,Human_Splice_Rec_2026043,Human_Splice_Rec_2026051,Human_Splice_Rec_2026065,Human_Splice_Rec_2026072,Human_Splice_Rec_2026073,Human_Splice_Rec_2026086,Human_Splice_Rec_2026087,Human_Splice_Rec_2026092,Human_Splice_Rec_2026093,Human_Splice_Rec_2026100,Human_Splice_Rec_2026101 RMVar_hsa_circ_195670,RMVar_hsa_circ_374845 14973 RMVar_ID_14973 Human_SNP_ID_667989764 A-to-I Human chr19 - 48254558 48254558 48254558 TTTAGTAGAGACGGGGTTTCACTATGTTGGCCAGGCTGGTCTCGAACCCCTGACTTGTGATCTGC TTTAGTAGAGACGGGGTTTCACTATGTTGGCCGGGCTGGTCTCGAACCCCTGACTTGTGATCTGC T C CARD8 Ensembl:ENSG00000105483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs970347071 Functional Loss SNV dbSNP153 33..33 33 - - - 14974 RMVar_ID_14974 Human_SNP_ID_667990010 A-to-I Human chr19 - 48255652 48255652 48255652 ACGACAAAGTGAGAAGTTCATATGAGCGTGTCAGAAGGGGAAATAGGGCCCCTCCCTTGTTAAAA ACGACAAAGTGAGAAGTTCATATGAGCGTGTCGGAAGGGGAAATAGGGCCCCTCCCTTGTTAAAA T C CARD8 Ensembl:ENSG00000105483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985352951 Functional Loss SNV dbSNP153 33..33 33 - - - 14975 RMVar_ID_14975 Human_SNP_ID_667990068 A-to-I Human chr19 - 48255876 48255876 48255876 TGCGAGCGTTATTTCAAAAGAAGTTGAGAACCAGAGAAACCGACCTAAGGGGATTCTCCCATTTG TGCGAGCGTTATTTCAAAAGAAGTTGAGAACCGGAGAAACCGACCTAAGGGGATTCTCCCATTTG T C CARD8 Ensembl:ENSG00000105483 Protein coding 5'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1169679166 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2025681,Human_Splice_Rec_2025719,Human_Splice_Rec_2025809,Human_Splice_Rec_2025837,Human_Splice_Rec_2025973,Human_Splice_Rec_2026041,Human_Splice_Rec_2026071,Human_Splice_Rec_2026085,Human_Splice_Rec_2026091,Human_Splice_Rec_2026099 14976 RMVar_ID_14976 Human_SNP_ID_667990190 A-to-I Human chr19 + 48256385 48256385 48256385 GAAGTCTCCGTCTGTCACCCAGGCTGGAGTGTAATGGAGCAATCTCGGCTCACTGCAACCTCTGC GAAGTCTCCGTCTGTCACCCAGGCTGGAGTGTGATGGAGCAATCTCGGCTCACTGCAACCTCTGC A G CARD8-AS1 Ensembl:ENSG00000268001 lincRNA exon GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1192541620 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2026114 14977 RMVar_ID_14977 Human_SNP_ID_667990192 A-to-I Human chr19 + 48256393 48256393 48256393 CGTCTGTCACCCAGGCTGGAGTGTAATGGAGCAATCTCGGCTCACTGCAACCTCTGCCTCCCAGG CGTCTGTCACCCAGGCTGGAGTGTAATGGAGCGATCTCGGCTCACTGCAACCTCTGCCTCCCAGG A G CARD8-AS1 Ensembl:ENSG00000268001 lincRNA exon GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs141894608 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2026114 14978 RMVar_ID_14978 Human_SNP_ID_667990223 A-to-I Human chr19 + 48256511 48256511 48256511 GCCACCACGCTCGGCTAATTTTTTGTATTTTTAGTAAAGACGGAGTTTCACCATGTTGGTCAGGA GCCACCACGCTCGGCTAATTTTTTGTATTTTTCGTAAAGACGGAGTTTCACCATGTTGGTCAGGA A C CARD8-AS1 Ensembl:ENSG00000268001 lincRNA exon GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs548939460 Functional Loss SNV dbSNP153 33..33 33 - - - 14979 RMVar_ID_14979 Human_SNP_ID_667990224 A-to-I Human chr19 + 48256511 48256511 48256511 GCCACCACGCTCGGCTAATTTTTTGTATTTTTAGTAAAGACGGAGTTTCACCATGTTGGTCAGGA GCCACCACGCTCGGCTAATTTTTTGTATTTTTGGTAAAGACGGAGTTTCACCATGTTGGTCAGGA A G CARD8-AS1 Ensembl:ENSG00000268001 lincRNA exon GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs548939460 Functional Loss SNV dbSNP153 33..33 33 - - - 14980 RMVar_ID_14980 Human_SNP_ID_667990461 A-to-I Human chr19 + 48257681 48257681 48257681 AGCTACTTGGGAGGCTGAGGAGGAGACTCACTAGAACTCAGGAAGCAGAGGTTGCAGTGAGCCAA AGCTACTTGGGAGGCTGAGGAGGAGACTCACTGGAACTCAGGAAGCAGAGGTTGCAGTGAGCCAA A G CARD8-AS1 Ensembl:ENSG00000268001 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1484193993 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8199732 14981 RMVar_ID_14981 Human_SNP_ID_667990474 A-to-I Human chr19 + 48257738 48257738 48257738 TGAGCCAAGACTGCGCCACTGCACTCTGGCCTAAGCAACAGAGGGAGACTCCATCTCAAAAAAAA TGAGCCAAGACTGCGCCACTGCACTCTGGCCTGAGCAACAGAGGGAGACTCCATCTCAAAAAAAA A G CARD8-AS1 Ensembl:ENSG00000268001 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs767821565 Functional Loss SNV dbSNP153 33..33 33 - - - 14982 RMVar_ID_14982 Human_SNP_ID_668004120 A-to-I Human chr19 - 48305533 48305533 48305533 GGGCATGGTGGCGGGTGTCTGTGGTCCCAGCTACTTGGGAGGCTGAGGTGGGAGGATTGCTTGAG GGGCATGGTGGCGGGTGTCTGTGGTCCCAGCTTCTTGGGAGGCTGAGGTGGGAGGATTGCTTGAG T A CCDC114 Ensembl:ENSG00000105479 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs897765790 Functional Loss SNV dbSNP153 33..33 33 - - - 14983 RMVar_ID_14983 Human_SNP_ID_668012208 A-to-I Human chr19 - 48334731 48334731 48334731 AAAAAATATCGGGCTTGGTGGCGCACACCTGTAGTCCCAGCTACTTAGGAGGCCAAGGCGGGAGG AAAAAATATCGGGCTTGGTGGCGCACACCTGTGGTCCCAGCTACTTAGGAGGCCAAGGCGGGAGG T C TMEM143 Ensembl:ENSG00000161558 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1018386381 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_195677,RMVar_hsa_circ_78870,RMVar_hsa_circ_126562,RMVar_hsa_circ_195678 14984 RMVar_ID_14984 Human_SNP_ID_668045516 A-to-I Human chr19 + 48453521 48453520 48453522 CACCACACCCCGTTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGG CACCACACCCCGTTAATTTTTGTATTTTTAGT__AGACGGGGTTTCACCATGTTGGCCAGGCTGG TAG T GRWD1 Ensembl:ENSG00000105447 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1377374184 Functional Loss DEL dbSNP153 33..34 33 - - - 14985 RMVar_ID_14985 Human_SNP_ID_668046699 A-to-I Human chr19 + 48457947 48457947 48457947 ACCTCAAATGATCTGCCTACCTTGGCCTCCCAAAGTCCTGGGATTACAGGTGCGAGCCACCGCAC ACCTCAAATGATCTGCCTACCTTGGCCTCCCACAGTCCTGGGATTACAGGTGCGAGCCACCGCAC A C KCNJ14 Ensembl:ENSG00000182324 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs60651902 Functional Loss SNV dbSNP153 33..33 33 - - - 14986 RMVar_ID_14986 Human_SNP_ID_668046877 A-to-I Human chr19 + 48458815 48458815 48458815 AAAAATTAGCTGGGATGGTGGCATGAGCCTGTAATTCCAGATACTCAGGAGGCTGAGGCAAGAGA AAAAATTAGCTGGGATGGTGGCATGAGCCTGTCATTCCAGATACTCAGGAGGCTGAGGCAAGAGA A C KCNJ14 Ensembl:ENSG00000182324 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1315368037 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13491481 14987 RMVar_ID_14987 Human_SNP_ID_668047125 A-to-I Human chr19 + 48459507 48459507 48459507 GCCTCAAACTCCTGGGCTTAAGCAATCCTCCCACCTCAACCTTCCAAGTAACTAGGACTACAGGT GCCTCAAACTCCTGGGCTTAAGCAATCCTCCCGCCTCAACCTTCCAAGTAACTAGGACTACAGGT A G KCNJ14 Ensembl:ENSG00000182324 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs983720470 Functional Loss SNV dbSNP153 33..33 33 - - - 14988 RMVar_ID_14988 Human_SNP_ID_668047210 A-to-I Human chr19 + 48459867 48459867 48459867 CCTGGCCAACATGGTGAAACCCCATCTCCACTAAAAATACAAAAGTTAGCCAGGCGTGGTGGCAT CCTGGCCAACATGGTGAAACCCCATCTCCACTGAAAATACAAAAGTTAGCCAGGCGTGGTGGCAT A G KCNJ14 Ensembl:ENSG00000182324 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1383850203 Functional Loss SNV dbSNP153 33..33 33 - - - 14989 RMVar_ID_14989 Human_SNP_ID_668047394 A-to-I Human chr19 + 48460523 48460523 48460523 CCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAACCACCACACCCGGCAGTCTTGGGGAAGT CCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAACCACCACACCCGGCAGTCTTGGGGAAGT A G KCNJ14 Ensembl:ENSG00000182324 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs539129539 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13491528,Human_RBP_ID_23179748 14990 RMVar_ID_14990 Human_SNP_ID_668047542 A-to-I Human chr19 + 48461226 48461226 48461226 CCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGCGAATCACTTGAACCTGGGAGGCAGAGGTT CCTGTAATCCCAGCTACTTGGGAGGCTGAGGCCGGCGAATCACTTGAACCTGGGAGGCAGAGGTT A C KCNJ14 Ensembl:ENSG00000182324 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1287787376 Functional Loss SNV dbSNP153 33..33 33 - - - 14991 RMVar_ID_14991 Human_SNP_ID_668047549 A-to-I Human chr19 + 48461240 48461240 48461240 TACTTGGGAGGCTGAGGCAGGCGAATCACTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCTGAGG TACTTGGGAGGCTGAGGCAGGCGAATCACTTGGACCTGGGAGGCAGAGGTTGCAGTGAGCTGAGG A G KCNJ14 Ensembl:ENSG00000182324 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs535255340 Functional Loss SNV dbSNP153 33..33 33 - - - 14992 RMVar_ID_14992 Human_SNP_ID_668047622 A-to-I Human chr19 + 48461483 48461483 48461483 TTGGGACGCGGAGATTGCAGTAAGCCAGGATCATGCCACTGCACTCCAGCTTGGGCGACAGAGCG TTGGGACGCGGAGATTGCAGTAAGCCAGGATCGTGCCACTGCACTCCAGCTTGGGCGACAGAGCG A G KCNJ14 Ensembl:ENSG00000182324 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1199815195 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22974983 14993 RMVar_ID_14993 Human_SNP_ID_668049190 A-to-I Human chr19 + 48466149 48466149 48466149 CCGCCCAGGCTGGAGTGCAATGGCGTGATCTCAGCTCACTGCAACCTCCGCCTCCCGGCTTCAAG CCGCCCAGGCTGGAGTGCAATGGCGTGATCTCTGCTCACTGCAACCTCCGCCTCCCGGCTTCAAG A T AC008403.1,KCNJ14 Ensembl:ENSG00000268465,Ensembl:ENSG00000182324 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1410133012 Functional Loss SNV dbSNP153 33..33 33 - - - 14994 RMVar_ID_14994 Human_SNP_ID_668095863 A-to-I Human chr19 - 48618952 48618952 48618952 GATGGGTCAGTCATAGCCTACCGCCCCCACTTAGTAGATGACCAAGTGGAGGTACTCGGAGGCTG GATGGGTCAGTCATAGCCTACCGCCCCCACTTGGTAGATGACCAAGTGGAGGTACTCGGAGGCTG T C RPL18 Ensembl:ENSG00000063177 Protein coding intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs903920264 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17696174 RMVar_hsa_circ_79282,RMVar_hsa_circ_195698,RMVar_hsa_circ_128150,RMVar_hsa_circ_344171,RMVar_hsa_circ_195705 14995 RMVar_ID_14995 Human_SNP_ID_668096497 A-to-I Human chr19 + 48620714 48620714 48620714 GGGAGGCCAAGGCCTGCGGATCACCTGAGGCCAGGAGTTCGAGATCAGCCTGGCCAACATGGTGA GGGAGGCCAAGGCCTGCGGATCACCTGAGGCCGGGAGTTCGAGATCAGCCTGGCCAACATGGTGA A G SPHK2 Ensembl:ENSG00000063176 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs562016577 Functional Loss SNV dbSNP153 33..33 33 - - - 14996 RMVar_ID_14996 Human_SNP_ID_668097177 A-to-I Human chr19 + 48623097 48623097 48623097 AAACCCTGTCTCTACTAAAAATGTAAAAAATTAGCCGGACGTGGTGGCACGTGCCTCTAGTCCCA AAACCCTGTCTCTACTAAAAATGTAAAAAATTGGCCGGACGTGGTGGCACGTGCCTCTAGTCCCA A G SPHK2 Ensembl:ENSG00000063176 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1243692467 Functional Loss SNV dbSNP153 33..33 33 - - - 14997 RMVar_ID_14997 Human_SNP_ID_668128369 A-to-I Human chr19 - 48727838 48727838 48727838 ACTAAAAATGCAAAAAATTAGCCGGGCATGGTAGCACATGCCTGTAATCCCAGCTACTTGGGAGG ACTAAAAATGCAAAAAATTAGCCGGGCATGGTGGCACATGCCTGTAATCCCAGCTACTTGGGAGG T C RASIP1 Ensembl:ENSG00000105538 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1218959457 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9617 14998 RMVar_ID_14998 Human_SNP_ID_668128370 A-to-I Human chr19 - 48727838 48727838 48727838 ACTAAAAATGCAAAAAATTAGCCGGGCATGGTAGCACATGCCTGTAATCCCAGCTACTTGGGAGG ACTAAAAATGCAAAAAATTAGCCGGGCATGGTCGCACATGCCTGTAATCCCAGCTACTTGGGAGG T G RASIP1 Ensembl:ENSG00000105538 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1218959457 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9617 14999 RMVar_ID_14999 Human_SNP_ID_668132927 A-to-I Human chr19 - 48743847 48743847 48743847 AGCTGGGATTACAGGTGCCCGCCATCACACCCAGCTAATTTTTGTATTTTTAGCAGAGACGGGGT AGCTGGGATTACAGGTGCCCGCCATCACACCCGGCTAATTTTTGTATTTTTAGCAGAGACGGGGT T C IZUMO1 Ensembl:ENSG00000182264 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1239302814 Functional Loss SNV dbSNP153 33..33 33 - - - 15000 RMVar_ID_15000 Human_SNP_ID_668150241 A-to-I Human chr19 - 48800747 48800747 48800747 TGGAGTGCAGTGGCATGATCGTGGCTCACTGCAGTCTCAAACTCCCAGGCTCAAGTGATCCTCCC TGGAGTGCAGTGGCATGATCGTGGCTCACTGCTGTCTCAAACTCCCAGGCTCAAGTGATCCTCCC T A BCAT2 Ensembl:ENSG00000105552 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1184219722 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10100,RMVar_hsa_circ_195722 15001 RMVar_ID_15001 Human_SNP_ID_668150317 A-to-I Human chr19 - 48801063 48801063 48801063 GAATCACTTGGACCTGGGAGGCGGAGGTTGCAATCAGCAGAGATCACGCCACTGCACTCCAGCCT GAATCACTTGGACCTGGGAGGCGGAGGTTGCAGTCAGCAGAGATCACGCCACTGCACTCCAGCCT T C BCAT2 Ensembl:ENSG00000105552 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1438194906 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13492576 RMVar_hsa_circ_10100,RMVar_hsa_circ_195722 15002 RMVar_ID_15002 Human_SNP_ID_668154788 A-to-I Human chr19 - 48816964 48816964 48816964 TGGTGTGGGGGCACATGCCTGTAGTCCCAGCTACTCGGGAAGCCGAGGCAGGAGAATTGCTTGAA TGGTGTGGGGGCACATGCCTGTAGTCCCAGCTGCTCGGGAAGCCGAGGCAGGAGAATTGCTTGAA T C HSD17B14 Ensembl:ENSG00000087076 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1014606844 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51872 15003 RMVar_ID_15003 Human_SNP_ID_668157234 A-to-I Human chr19 - 48825959 48825959 48825959 AAAAATAGCTGTGCGCGGTGGCGGGTGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGTGGGAGA AAAAATAGCTGTGCGCGGTGGCGGGTGCCTGTTGTCCCAGCTACTCGGGAGGCTGAGGTGGGAGA T A HSD17B14 Ensembl:ENSG00000087076 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1366798568 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_139450 RMVar_hsa_circ_51872 15004 RMVar_ID_15004 Human_SNP_ID_668157749 A-to-I Human chr19 - 48827292 48827292 48827292 ATGTCTTTGTAATCCCAGCACTTTGGGAGGCTAAGGCGGGCAGATCATGAGGTCAGGAGTTCGAG ATGTCTTTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGCAGATCATGAGGTCAGGAGTTCGAG T C HSD17B14 Ensembl:ENSG00000087076 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs559566482 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51872 15005 RMVar_ID_15005 Human_SNP_ID_668158072 A-to-I Human chr19 - 48828452 48828452 48828452 CACTATGACTGACTAATTTTTAACTTTTTTGTAGAGACAGGGTCTTTCTATGCTGCTCAGGCTGG CACTATGACTGACTAATTTTTAACTTTTTTGTTGAGACAGGGTCTTTCTATGCTGCTCAGGCTGG T A HSD17B14 Ensembl:ENSG00000087076 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1232572816 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51872 15006 RMVar_ID_15006 Human_SNP_ID_668158378 A-to-I Human chr19 - 48829784 48829784 48829784 ACAAAATTAGCCGGGTGTGGTGGCACATGCCTATAATCCCAGCTACTCAGGAGGCTGAGGCAGGA ACAAAATTAGCCGGGTGTGGTGGCACATGCCTCTAATCCCAGCTACTCAGGAGGCTGAGGCAGGA T G HSD17B14 Ensembl:ENSG00000087076 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1238379037 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51872 15007 RMVar_ID_15007 Human_SNP_ID_668180477 A-to-I Human chr19 + 48902624 48902624 48902624 TAGAGACAGGGTGTCATTATACTGCCCAGGCTAGTCTCGAACTCCTGAGTTCAAGTGATTTGCCC TAGAGACAGGGTGTCATTATACTGCCCAGGCTGGTCTCGAACTCCTGAGTTCAAGTGATTTGCCC A G NUCB1 Ensembl:ENSG00000104805 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1279056417 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_195733,RMVar_hsa_circ_94007 15008 RMVar_ID_15008 Human_SNP_ID_668181867 A-to-I Human chr19 + 48907181 48907181 48907181 TATTTTTAGTAGAGACGGAATTTCACTGTATTAGCCAGGATGGTCTTGATCTCTAACCTCGTGAT TATTTTTAGTAGAGACGGAATTTCACTGTATTGGCCAGGATGGTCTTGATCTCTAACCTCGTGAT A G NUCB1 Ensembl:ENSG00000104805 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1470573887 Functional Loss SNV dbSNP153 33..33 33 - - - 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 15009 RMVar_ID_15009 Human_SNP_ID_668182656 A-to-I Human chr19 + 48909714 48909714 48909714 CAGGCACACACCACTGCACACAGCTAATTTTTATATTTTTTGTAGAGATGGGGTTTCACCATGTT CAGGCACACACCACTGCACACAGCTAATTTTTGTATTTTTTGTAGAGATGGGGTTTCACCATGTT A G NUCB1 Ensembl:ENSG00000104805 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1018856572 Functional Loss SNV dbSNP153 33..33 33 - - - 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 15010 RMVar_ID_15010 Human_SNP_ID_668186900 A-to-I Human chr19 + 48923695 48923695 48923695 TGCATTGTTTTAGTAGTGATGGGGGTTTCACCATATTGGCCAGGCTGGTCTTGAACTCCTGACAT TGCATTGTTTTAGTAGTGATGGGGGTTTCACCGTATTGGCCAGGCTGGTCTTGAACTCCTGACAT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1201612009 Functional Loss SNV dbSNP153 33..33 33 - - - 15011 RMVar_ID_15011 Human_SNP_ID_668186912 A-to-I Human chr19 + 48923745 48923745 48923745 TTGAACTCCTGACATCATGATCTGCCCACCTTAGCCTCCCAAAGTGCTGGGATTACAGGAGTGAG TTGAACTCCTGACATCATGATCTGCCCACCTTGGCCTCCCAAAGTGCTGGGATTACAGGAGTGAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037891841 Functional Loss SNV dbSNP153 33..33 33 - - - 15012 RMVar_ID_15012 Human_SNP_ID_668186947 A-to-I Human chr19 + 48923855 48923855 48923855 GGCCAGGTGCTGTGGCTCACGCCTGTAATCCCAACACTTCGAAAGGCCAAGATAGGGGGGATCAC GGCCAGGTGCTGTGGCTCACGCCTGTAATCCCCACACTTCGAAAGGCCAAGATAGGGGGGATCAC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1438801104 Functional Loss SNV dbSNP153 33..33 33 - - - 15013 RMVar_ID_15013 Human_SNP_ID_668186948 A-to-I Human chr19 + 48923855 48923855 48923855 GGCCAGGTGCTGTGGCTCACGCCTGTAATCCCAACACTTCGAAAGGCCAAGATAGGGGGGATCAC GGCCAGGTGCTGTGGCTCACGCCTGTAATCCCGACACTTCGAAAGGCCAAGATAGGGGGGATCAC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1438801104 Functional Loss SNV dbSNP153 33..33 33 - - - 15014 RMVar_ID_15014 Human_SNP_ID_668187005 A-to-I Human chr19 + 48924055 48924054 48924056 TTGATCCTGGGAGGCGGAGGTTGCAGCGAGCCAAGATTGCACCACTGCACTCCAACCGGAGTACC TTGATCCTGGGAGGCGGAGGTTGCAGCGAGCC__GATTGCACCACTGCACTCCAACCGGAGTACC CAA C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1224153159 Functional Loss DEL dbSNP153 33..34 33 - - - 15015 RMVar_ID_15015 Human_SNP_ID_668187345 A-to-I Human chr19 + 48925332 48925332 48925332 TGGTCAGGCTGGTCTTGAGAACTCCTGACCTCAGGTGATCCCCCCGCCTCGGCCTCCCACAGTGT TGGTCAGGCTGGTCTTGAGAACTCCTGACCTCTGGTGATCCCCCCGCCTCGGCCTCCCACAGTGT A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1475172031 Functional Loss SNV dbSNP153 33..33 33 - - - 15016 RMVar_ID_15016 Human_SNP_ID_668187494 A-to-I Human chr19 + 48925651 48925651 48925651 TGCACCTGTGGTCCCAGCTACTCAGGAGGCTTAAGGACAGAAGAATCGCTTGGCCACAGAAGGTT TGCACCTGTGGTCCCAGCTACTCAGGAGGCTTCAGGACAGAAGAATCGCTTGGCCACAGAAGGTT A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1205180963 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13493140 15017 RMVar_ID_15017 Human_SNP_ID_668187497 A-to-I Human chr19 + 48925659 48925659 48925659 TGGTCCCAGCTACTCAGGAGGCTTAAGGACAGAAGAATCGCTTGGCCACAGAAGGTTAAGGCTAC TGGTCCCAGCTACTCAGGAGGCTTAAGGACAGGAGAATCGCTTGGCCACAGAAGGTTAAGGCTAC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs952068045 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13493140 15018 RMVar_ID_15018 Human_SNP_ID_668187539 A-to-I Human chr19 + 48925789 48925789 48925789 AATAAATAGGCCGGGCACAGTGGCTGATGCCTATAATCCCAACGCTTCAGGAGGCCAAGGAGGAA AATAAATAGGCCGGGCACAGTGGCTGATGCCTGTAATCCCAACGCTTCAGGAGGCCAAGGAGGAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1016416348 Functional Loss SNV dbSNP153 33..33 33 - - - 15019 RMVar_ID_15019 Human_SNP_ID_668197150 A-to-I Human chr19 + 48958149 48958149 48958149 GTCTTGCTCTGTTGGCCAGGCTGGAGTGCAGTAGTGATCATAGCTCACTGCAGCCTCAAACCGCT GTCTTGCTCTGTTGGCCAGGCTGGAGTGCAGTGGTGATCATAGCTCACTGCAGCCTCAAACCGCT A G BAX Ensembl:ENSG00000087088 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1050537157 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13493317,Human_RBP_ID_22720499,Human_RBP_ID_23804048 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 15020 RMVar_ID_15020 Human_SNP_ID_668197165 A-to-I Human chr19 + 48958192 48958192 48958192 CTCACTGCAGCCTCAAACCGCTGGGGTCAAGCAGTTCTCTCGCCTCAGTCTCCAGAGTAGCTGAG CTCACTGCAGCCTCAAACCGCTGGGGTCAAGCTGTTCTCTCGCCTCAGTCTCCAGAGTAGCTGAG A T BAX Ensembl:ENSG00000087088 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1486336149 Functional Loss SNV dbSNP153 33..33 33 - - - 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 15021 RMVar_ID_15021 Human_SNP_ID_668197315 A-to-I Human chr19 + 48958673 48958673 48958673 TTAAGCGATTCTCTTGCCTCAGTCTCCCGAGTAGCTTGGGATTACAGGCGTCCGCCACCACACCC TTAAGCGATTCTCTTGCCTCAGTCTCCCGAGTTGCTTGGGATTACAGGCGTCCGCCACCACACCC A T BAX Ensembl:ENSG00000087088 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1395104804 Functional Loss SNV dbSNP153 33..33 33 - - - 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 15022 RMVar_ID_15022 Human_SNP_ID_668197348 A-to-I Human chr19 + 48958806 48958806 48958806 ACCTCAGGTGATCCGCCTGCCTCGGTCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGTGC ACCTCAGGTGATCCGCCTGCCTCGGTCTCCCAGAGTGCTGGGATTACAGGCGTGAGCCACCGTGC A G BAX Ensembl:ENSG00000087088 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1234014539 Functional Loss SNV dbSNP153 33..33 33 - - - 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 15023 RMVar_ID_15023 Human_SNP_ID_668197350 A-to-I Human chr19 + 48958819 48958819 48958819 CGCCTGCCTCGGTCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGTGCTCAGCTGAGAGGG CGCCTGCCTCGGTCTCCCAAAGTGCTGGGATTTCAGGCGTGAGCCACCGTGCTCAGCTGAGAGGG A T BAX Ensembl:ENSG00000087088 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1045646416 Functional Loss SNV dbSNP153 33..33 33 - - - 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 15024 RMVar_ID_15024 Human_SNP_ID_668197463 A-to-I Human chr19 + 48959239 48959239 48959239 GGGCATGGTGGTGGGCACTTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGAAGAATGGCGTGAA GGGCATGGTGGTGGGCACTTGTAGTCCCAGCTGCTCGGGAGGCTGAGGCAGAAGAATGGCGTGAA A G BAX Ensembl:ENSG00000087088 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1301197796 Functional Loss SNV dbSNP153 33..33 33 - - - 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 15025 RMVar_ID_15025 Human_SNP_ID_668197650 A-to-I Human chr19 + 48959783 48959783 48959783 GGGAGGCGGAGGTTGCAATGAGCCGAGACTGCACTATTGTACTCCAGCCTGGGCAACAAGATCAA GGGAGGCGGAGGTTGCAATGAGCCGAGACTGCCCTATTGTACTCCAGCCTGGGCAACAAGATCAA A C BAX Ensembl:ENSG00000087088 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11669164 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25429372 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 15026 RMVar_ID_15026 Human_SNP_ID_668197651 A-to-I Human chr19 + 48959783 48959783 48959783 GGGAGGCGGAGGTTGCAATGAGCCGAGACTGCACTATTGTACTCCAGCCTGGGCAACAAGATCAA GGGAGGCGGAGGTTGCAATGAGCCGAGACTGCGCTATTGTACTCCAGCCTGGGCAACAAGATCAA A G BAX Ensembl:ENSG00000087088 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11669164 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25429372 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 15027 RMVar_ID_15027 Human_SNP_ID_668197794 A-to-I Human chr19 + 48960213 48960213 48960213 CAATTTTATTTTTTTTATTTATTTATTTTTTGAGACGGATTCTTGCTCTATTGTCCAGGCTGGCG CAATTTTATTTTTTTTATTTATTTATTTTTTGGGACGGATTCTTGCTCTATTGTCCAGGCTGGCG A G BAX Ensembl:ENSG00000087088 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1283232543 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6778333,Human_RBP_ID_13493342 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 15028 RMVar_ID_15028 Human_SNP_ID_668202247 A-to-I Human chr19 - 48972667 48972667 48972667 TGAGACCAGCCTGGCCAACATGGTGAAACCCTATCTCTACTACAAATACAAAAATTAGCTGGGGG TGAGACCAGCCTGGCCAACATGGTGAAACCCTGTCTCTACTACAAATACAAAAATTAGCTGGGGG T C GYS1 Ensembl:ENSG00000104812 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs975306822 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33593,RMVar_hsa_circ_371698,RMVar_hsa_circ_376458,RMVar_hsa_circ_92672,RMVar_hsa_circ_195760,RMVar_hsa_circ_340123,RMVar_hsa_circ_195761,RMVar_hsa_circ_195762 15029 RMVar_ID_15029 Human_SNP_ID_668202547 A-to-I Human chr19 - 48973718 48973718 48973718 GGTCAGGAGTTTGAGACCAGCCTGGCCAATATAGTGAAACCCTGTCTCTACTAAAAATACAAAAA GGTCAGGAGTTTGAGACCAGCCTGGCCAATATGGTGAAACCCTGTCTCTACTAAAAATACAAAAA T C GYS1 Ensembl:ENSG00000104812 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1352429925 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33593,RMVar_hsa_circ_371698,RMVar_hsa_circ_376458,RMVar_hsa_circ_92672,RMVar_hsa_circ_195760,RMVar_hsa_circ_340123,RMVar_hsa_circ_195761,RMVar_hsa_circ_195762 15030 RMVar_ID_15030 Human_SNP_ID_668203621 A-to-I Human chr19 - 48977438 48977438 48977438 CAGGCACATGCCACCACACCCAGCTAATTTATATATTTTTAGTAGAAACGAGATTTCACCATGTT CAGGCACATGCCACCACACCCAGCTAATTTATGTATTTTTAGTAGAAACGAGATTTCACCATGTT T C GYS1 Ensembl:ENSG00000104812 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1411072285 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_371698,RMVar_hsa_circ_376458,RMVar_hsa_circ_98364,RMVar_hsa_circ_92672,RMVar_hsa_circ_195760,RMVar_hsa_circ_340123,RMVar_hsa_circ_195761,RMVar_hsa_circ_195762,RMVar_hsa_circ_295862,RMVar_hsa_circ_195765,RMVar_hsa_circ_195766,RMVar_hsa_circ_50956 15031 RMVar_ID_15031 Human_SNP_ID_668204076 A-to-I Human chr19 - 48978821 48978821 48978821 ATCCTAGAAACCTAAGGGTAGCTGGGCGCGGCAGCTCATGCCTGTAATTCCAGCACTTTGGGAGG ATCCTAGAAACCTAAGGGTAGCTGGGCGCGGCGGCTCATGCCTGTAATTCCAGCACTTTGGGAGG T C GYS1 Ensembl:ENSG00000104812 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1362429915 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_371698,RMVar_hsa_circ_376458,RMVar_hsa_circ_59940,RMVar_hsa_circ_98364,RMVar_hsa_circ_195760,RMVar_hsa_circ_340123,RMVar_hsa_circ_195762,RMVar_hsa_circ_195766,RMVar_hsa_circ_352428,RMVar_hsa_circ_50956,RMVar_hsa_circ_32074,RMVar_hsa_circ_43236,RMVar_hsa_circ_195768 15032 RMVar_ID_15032 Human_SNP_ID_668204361 A-to-I Human chr19 - 48979610 48979610 48979610 GAAAGAGGCTGGGCGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGAGGGCAG GAAAGAGGCTGGGCGCGGTGGCTCACACCTGTGATCCCAGCACTTTGGGAGGCTGAGGAGGGCAG T C GYS1 Ensembl:ENSG00000104812 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1057335089 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_371698,RMVar_hsa_circ_376458,RMVar_hsa_circ_59940,RMVar_hsa_circ_98364,RMVar_hsa_circ_195760,RMVar_hsa_circ_340123,RMVar_hsa_circ_195762,RMVar_hsa_circ_195766,RMVar_hsa_circ_352428,RMVar_hsa_circ_50956,RMVar_hsa_circ_32074,RMVar_hsa_circ_43236,RMVar_hsa_circ_195768 15033 RMVar_ID_15033 Human_SNP_ID_668204472 A-to-I Human chr19 - 48979848 48979848 48979848 GAGGTCGGGAGTTTGAGACCAGCTTGACCAACATGGTGAAACCCCGTCTTTCCTAAAAATAAAAA GAGGTCGGGAGTTTGAGACCAGCTTGACCAACGTGGTGAAACCCCGTCTTTCCTAAAAATAAAAA T C GYS1 Ensembl:ENSG00000104812 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs916426303 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_371698,RMVar_hsa_circ_376458,RMVar_hsa_circ_59940,RMVar_hsa_circ_98364,RMVar_hsa_circ_195760,RMVar_hsa_circ_340123,RMVar_hsa_circ_195762,RMVar_hsa_circ_195766,RMVar_hsa_circ_352428,RMVar_hsa_circ_50956,RMVar_hsa_circ_32074,RMVar_hsa_circ_43236,RMVar_hsa_circ_195768 15034 RMVar_ID_15034 Human_SNP_ID_668204632 A-to-I Human chr19 - 48980436 48980436 48980436 TTGACCAGGCTGGTCTTGAACTCCTGACCTCAAGTGACCTGCCCTCCTCATGTATTCCAGGTCCT TTGACCAGGCTGGTCTTGAACTCCTGACCTCAGGTGACCTGCCCTCCTCATGTATTCCAGGTCCT T C GYS1 Ensembl:ENSG00000104812 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1261733303 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_371698,RMVar_hsa_circ_376458,RMVar_hsa_circ_59940,RMVar_hsa_circ_98364,RMVar_hsa_circ_195760,RMVar_hsa_circ_340123,RMVar_hsa_circ_195762,RMVar_hsa_circ_195766,RMVar_hsa_circ_352428,RMVar_hsa_circ_50956,RMVar_hsa_circ_32074,RMVar_hsa_circ_43236,RMVar_hsa_circ_195768 15035 RMVar_ID_15035 Human_SNP_ID_668204756 A-to-I Human chr19 - 48980898 48980896 48980898 ATTGGCCAGGCTGGTCTTGAACTCCTGACCTCAGGTGTTCCGCCTGCCTCAGCCTCCCAAAGTGC ATTGGCCAGGCTGGTCTTGAACTCCTGACCTC__GTGTTCCGCCTGCCTCAGCCTCCCAAAGTGC CCT C GYS1 Ensembl:ENSG00000104812 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1170645223 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_371698,RMVar_hsa_circ_376458,RMVar_hsa_circ_59940,RMVar_hsa_circ_98364,RMVar_hsa_circ_195760,RMVar_hsa_circ_340123,RMVar_hsa_circ_195762,RMVar_hsa_circ_195766,RMVar_hsa_circ_352428,RMVar_hsa_circ_50956,RMVar_hsa_circ_32074,RMVar_hsa_circ_43236,RMVar_hsa_circ_195768 15036 RMVar_ID_15036 Human_SNP_ID_668204757 A-to-I Human chr19 - 48980898 48980898 48980898 ATTGGCCAGGCTGGTCTTGAACTCCTGACCTCAGGTGTTCCGCCTGCCTCAGCCTCCCAAAGTGC ATTGGCCAGGCTGGTCTTGAACTCCTGACCTCGGGTGTTCCGCCTGCCTCAGCCTCCCAAAGTGC T C GYS1 Ensembl:ENSG00000104812 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1362191002 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_371698,RMVar_hsa_circ_376458,RMVar_hsa_circ_59940,RMVar_hsa_circ_98364,RMVar_hsa_circ_195760,RMVar_hsa_circ_340123,RMVar_hsa_circ_195762,RMVar_hsa_circ_195766,RMVar_hsa_circ_352428,RMVar_hsa_circ_50956,RMVar_hsa_circ_32074,RMVar_hsa_circ_43236,RMVar_hsa_circ_195768 15037 RMVar_ID_15037 Human_SNP_ID_668204782 A-to-I Human chr19 - 48980992 48980992 48980992 TTTCCTGCCTCAGCCTCTGAGTAGCTGGGACTACAGGGGTGTGCCACCACACCTGGCTAACTTTT TTTCCTGCCTCAGCCTCTGAGTAGCTGGGACTGCAGGGGTGTGCCACCACACCTGGCTAACTTTT T C GYS1 Ensembl:ENSG00000104812 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs948850508 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_371698,RMVar_hsa_circ_376458,RMVar_hsa_circ_59940,RMVar_hsa_circ_98364,RMVar_hsa_circ_195760,RMVar_hsa_circ_340123,RMVar_hsa_circ_195762,RMVar_hsa_circ_195766,RMVar_hsa_circ_352428,RMVar_hsa_circ_50956,RMVar_hsa_circ_32074,RMVar_hsa_circ_43236,RMVar_hsa_circ_195768 15038 RMVar_ID_15038 Human_SNP_ID_668204839 A-to-I Human chr19 - 48981158 48981158 48981158 TGCCCGCCTCAGCCTCCCAAAGTGCTGGAATTACAGGCATGAGCCACCGCACCCGGCCCTCTTTT TGCCCGCCTCAGCCTCCCAAAGTGCTGGAATTCCAGGCATGAGCCACCGCACCCGGCCCTCTTTT T G GYS1 Ensembl:ENSG00000104812 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1435873847 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_371698,RMVar_hsa_circ_376458,RMVar_hsa_circ_59940,RMVar_hsa_circ_98364,RMVar_hsa_circ_195760,RMVar_hsa_circ_340123,RMVar_hsa_circ_195762,RMVar_hsa_circ_195766,RMVar_hsa_circ_352428,RMVar_hsa_circ_50956,RMVar_hsa_circ_32074,RMVar_hsa_circ_43236,RMVar_hsa_circ_195768 15039 RMVar_ID_15039 Human_SNP_ID_668204853 A-to-I Human chr19 - 48981216 48981216 48981216 TAGAGATGGGGTTTCACCACATTGGCCAGACTAGTCTCAAACTCCTGATCTCGTGATCTGCCCGC TAGAGATGGGGTTTCACCACATTGGCCAGACTGGTCTCAAACTCCTGATCTCGTGATCTGCCCGC T C GYS1 Ensembl:ENSG00000104812 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1237886639 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_371698,RMVar_hsa_circ_376458,RMVar_hsa_circ_59940,RMVar_hsa_circ_98364,RMVar_hsa_circ_195760,RMVar_hsa_circ_340123,RMVar_hsa_circ_195762,RMVar_hsa_circ_195766,RMVar_hsa_circ_352428,RMVar_hsa_circ_50956,RMVar_hsa_circ_32074,RMVar_hsa_circ_43236,RMVar_hsa_circ_195768 15040 RMVar_ID_15040 Human_SNP_ID_668204858 A-to-I Human chr19 - 48981247 48981247 48981247 CACCATGCCTGGCTAATTTTTGTATTTTCAGTAGAGATGGGGTTTCACCACATTGGCCAGACTAG CACCATGCCTGGCTAATTTTTGTATTTTCAGTGGAGATGGGGTTTCACCACATTGGCCAGACTAG T C GYS1 Ensembl:ENSG00000104812 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs527707868 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_371698,RMVar_hsa_circ_376458,RMVar_hsa_circ_59940,RMVar_hsa_circ_98364,RMVar_hsa_circ_195760,RMVar_hsa_circ_340123,RMVar_hsa_circ_195762,RMVar_hsa_circ_195766,RMVar_hsa_circ_352428,RMVar_hsa_circ_50956,RMVar_hsa_circ_32074,RMVar_hsa_circ_43236,RMVar_hsa_circ_195768 15041 RMVar_ID_15041 Human_SNP_ID_668204864 A-to-I Human chr19 - 48981291 48981291 48981291 CATCTGCCTCAGCCTCTCGAGTAGCTGGGACTACAGGTGCACACCACCATGCCTGGCTAATTTTT CATCTGCCTCAGCCTCTCGAGTAGCTGGGACTGCAGGTGCACACCACCATGCCTGGCTAATTTTT T C GYS1 Ensembl:ENSG00000104812 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs888952458 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_371698,RMVar_hsa_circ_376458,RMVar_hsa_circ_59940,RMVar_hsa_circ_98364,RMVar_hsa_circ_195760,RMVar_hsa_circ_340123,RMVar_hsa_circ_195762,RMVar_hsa_circ_195766,RMVar_hsa_circ_352428,RMVar_hsa_circ_50956,RMVar_hsa_circ_32074,RMVar_hsa_circ_43236,RMVar_hsa_circ_195768 15042 RMVar_ID_15042 Human_SNP_ID_668204874 A-to-I Human chr19 - 48981331 48981331 48981331 TTGGCTCACTGCAACCTCCACCTCCTGGGTTCAAGCAAGTCATCTGCCTCAGCCTCTCGAGTAGC TTGGCTCACTGCAACCTCCACCTCCTGGGTTCCAGCAAGTCATCTGCCTCAGCCTCTCGAGTAGC T G GYS1 Ensembl:ENSG00000104812 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs901572991 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_371698,RMVar_hsa_circ_376458,RMVar_hsa_circ_59940,RMVar_hsa_circ_98364,RMVar_hsa_circ_195760,RMVar_hsa_circ_340123,RMVar_hsa_circ_195762,RMVar_hsa_circ_195766,RMVar_hsa_circ_352428,RMVar_hsa_circ_50956,RMVar_hsa_circ_32074,RMVar_hsa_circ_43236,RMVar_hsa_circ_195768 15043 RMVar_ID_15043 Human_SNP_ID_668206021 A-to-I Human chr19 - 48985144 48985144 48985144 AGGAGGCTGAGGTGGGAGGATTGCTCGAGCCTAGGAGGTCAAGGGTGCAGTGAGCTGTGATCGTG AGGAGGCTGAGGTGGGAGGATTGCTCGAGCCTGGGAGGTCAAGGGTGCAGTGAGCTGTGATCGTG T C GYS1 Ensembl:ENSG00000104812 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1023804629 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5671,RMVar_hsa_circ_371698,RMVar_hsa_circ_59940,RMVar_hsa_circ_195760,RMVar_hsa_circ_340123,RMVar_hsa_circ_195762,RMVar_hsa_circ_50956,RMVar_hsa_circ_43236,RMVar_hsa_circ_37533,RMVar_hsa_circ_83608,RMVar_hsa_circ_195771,RMVar_hsa_circ_195770,RMVar_hsa_circ_337060 15044 RMVar_ID_15044 Human_SNP_ID_668207304 A-to-I Human chr19 - 48989580 48989580 48989580 TCTCTACTAAAAATACAAAAAATTAGCCAGGCATGATGGTGCGTGCTCGTGATCCCAGTTACTCA TCTCTACTAAAAATACAAAAAATTAGCCAGGCGTGATGGTGCGTGCTCGTGATCCCAGTTACTCA T C GYS1 Ensembl:ENSG00000104812 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1375010211 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83608,RMVar_hsa_circ_195770 15045 RMVar_ID_15045 Human_SNP_ID_668243166 A-to-I Human chr19 + 49086763 49086763 49086763 GTGGTCGAGTGCGTCTGTAGTCTCAGCTACTCAGGAGGCTGAGGTGGGAGGATTGCTTGAGCCCA GTGGTCGAGTGCGTCTGTAGTCTCAGCTACTCCGGAGGCTGAGGTGGGAGGATTGCTTGAGCCCA A C SNRNP70 Ensembl:ENSG00000104852 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1167223916 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22592309 RMVar_hsa_circ_12770,RMVar_hsa_circ_369857,RMVar_hsa_circ_195801 15046 RMVar_ID_15046 Human_SNP_ID_668243541 A-to-I Human chr19 + 49088009 49088009 49088009 GCAGCCTCCGGTTCAAGCAGTTCTCCTGCCTCAGCCTCTCAAGTAGCTGGGATTACAGGCATGCA GCAGCCTCCGGTTCAAGCAGTTCTCCTGCCTCGGCCTCTCAAGTAGCTGGGATTACAGGCATGCA A G SNRNP70 Ensembl:ENSG00000104852 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1315198073 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12770,RMVar_hsa_circ_369857,RMVar_hsa_circ_195801 15047 RMVar_ID_15047 Human_SNP_ID_668243558 A-to-I Human chr19 + 49088071 49088071 49088071 GCACCACCACGCCTGGCTAATTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTAGGCCAGGC GCACCACCACGCCTGGCTAATTTTGTATTTTTCGTAGAGATGGGGTTTCACCATGTAGGCCAGGC A C SNRNP70 Ensembl:ENSG00000104852 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs546705306 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12770,RMVar_hsa_circ_369857,RMVar_hsa_circ_195801 15048 RMVar_ID_15048 Human_SNP_ID_668243759 A-to-I Human chr19 + 49088565 49088565 49088565 GTTGCCCAGGCTGGAGTGCAGTGGCGTGATCTAGGCTCACTGCAACTTCCACCTCCCGGGTTCAA GTTGCCCAGGCTGGAGTGCAGTGGCGTGATCTCGGCTCACTGCAACTTCCACCTCCCGGGTTCAA A C SNRNP70 Ensembl:ENSG00000104852 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1364084163 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12770,RMVar_hsa_circ_369857,RMVar_hsa_circ_195801 15049 RMVar_ID_15049 Human_SNP_ID_668243968 A-to-I Human chr19 + 49089427 49089427 49089427 TGAACCTGGGAAGCGGAGGTTGCAGTGAGCCCAGATCGCGCCATTGCACACCAGCCTGGGCAACA TGAACCTGGGAAGCGGAGGTTGCAGTGAGCCCCGATCGCGCCATTGCACACCAGCCTGGGCAACA A C SNRNP70 Ensembl:ENSG00000104852 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1263596867 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25429649 RMVar_hsa_circ_12770,RMVar_hsa_circ_369857,RMVar_hsa_circ_195801 15050 RMVar_ID_15050 Human_SNP_ID_668244148 A-to-I Human chr19 + 49089982 49089981 49089982 CTGCACCCGGCCTTTACACCTGGCTAATTTTTAAATTTTTTGTGGAGATGGTGTTTCACTGTGTT CTGCACCCGGCCTTTACACCTGGCTAATTTTT_AATTTTTTGTGGAGATGGTGTTTCACTGTGTT TA T SNRNP70 Ensembl:ENSG00000104852 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1237878956 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_13494085 RMVar_hsa_circ_12770,RMVar_hsa_circ_369857,RMVar_hsa_circ_195801 15051 RMVar_ID_15051 Human_SNP_ID_668244149 A-to-I Human chr19 + 49089982 49089982 49089982 CTGCACCCGGCCTTTACACCTGGCTAATTTTTAAATTTTTTGTGGAGATGGTGTTTCACTGTGTT CTGCACCCGGCCTTTACACCTGGCTAATTTTTGAATTTTTTGTGGAGATGGTGTTTCACTGTGTT A G SNRNP70 Ensembl:ENSG00000104852 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs539299427 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13494085 RMVar_hsa_circ_12770,RMVar_hsa_circ_369857,RMVar_hsa_circ_195801 15052 RMVar_ID_15052 Human_SNP_ID_668244791 A-to-I Human chr19 + 49092292 49092292 49092292 CACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGGCGGGGTTTCAGCATGTTGACCAGGATCG CACCACGCCCAGCTAATTTTTGTATTTTTAGTGGAGGCGGGGTTTCAGCATGTTGACCAGGATCG A G SNRNP70 Ensembl:ENSG00000104852 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1303928452 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13494150,Human_RBP_ID_22592311 RMVar_hsa_circ_369069 15053 RMVar_ID_15053 Human_SNP_ID_668245079 A-to-I Human chr19 + 49093170 49093170 49093170 CAGGCTGGAGTGTAGTGGTACGATCTAGGGTCACTGCAACCTCTGCCTCCCCGGTTCAAGCGATT CAGGCTGGAGTGTAGTGGTACGATCTAGGGTCGCTGCAACCTCTGCCTCCCCGGTTCAAGCGATT A G SNRNP70 Ensembl:ENSG00000104852 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1334250247 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5499946,Human_RBP_ID_13494174 RMVar_hsa_circ_369069 15054 RMVar_ID_15054 Human_SNP_ID_668245371 A-to-I Human chr19 + 49093889 49093889 49093889 CAAAAACAAAACAAAACCTAGCCAGGCATTGTAGTGGGCTCCTGTAATCCCAGCTACTCGGGAGG CAAAAACAAAACAAAACCTAGCCAGGCATTGTGGTGGGCTCCTGTAATCCCAGCTACTCGGGAGG A G SNRNP70 Ensembl:ENSG00000104852 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1428125672 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_369069 15055 RMVar_ID_15055 Human_SNP_ID_668246006 A-to-I Human chr19 + 49096151 49096151 49096151 ATGATCTCGGCTCACTGCAATCTCCACCTCCCAGATTCAAGCAATTCTCCTGCGTCAGCCTCCCG ATGATCTCGGCTCACTGCAATCTCCACCTCCCGGATTCAAGCAATTCTCCTGCGTCAGCCTCCCG A G SNRNP70 Ensembl:ENSG00000104852 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1370843654 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_369069 15056 RMVar_ID_15056 Human_SNP_ID_668246135 A-to-I Human chr19 + 49096584 49096584 49096584 GGTCAGGAGTTCGAAACCAGCCTGGCCAACATAGTGAAACCCCGTCTCTACTAAAAATACAAAAG GGTCAGGAGTTCGAAACCAGCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAG A G SNRNP70 Ensembl:ENSG00000104852 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1326715295 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_369069 15057 RMVar_ID_15057 Human_SNP_ID_668246137 A-to-I Human chr19 + 49096589 49096589 49096589 GGAGTTCGAAACCAGCCTGGCCAACATAGTGAAACCCCGTCTCTACTAAAAATACAAAAGATTAG GGAGTTCGAAACCAGCCTGGCCAACATAGTGATACCCCGTCTCTACTAAAAATACAAAAGATTAG A T SNRNP70 Ensembl:ENSG00000104852 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1268539389 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_369069 15058 RMVar_ID_15058 Human_SNP_ID_668249111 A-to-I Human chr19 - 49105903 49105902 49105904 GTCAATCAAATGTGCCCACCCCGAAACAAGAGACTCATCCAGGACTGAGTGTAAAGCTGGGGCCT GTCAATCAAATGTGCCCACCCCGAAACAAGA__CTCATCCAGGACTGAGTGTAAAGCTGGGGCCT GTC G - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1445371520 Functional Loss DEL dbSNP153 32..33 33 - - - 15059 RMVar_ID_15059 Human_SNP_ID_668249112 A-to-I Human chr19 - 49105903 49105903 49105903 GTCAATCAAATGTGCCCACCCCGAAACAAGAGACTCATCCAGGACTGAGTGTAAAGCTGGGGCCT GTCAATCAAATGTGCCCACCCCGAAACAAGAGGCTCATCCAGGACTGAGTGTAAAGCTGGGGCCT T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1213800152 Functional Loss SNV dbSNP153 33..33 33 - - - 15060 RMVar_ID_15060 Human_SNP_ID_668272127 A-to-I Human chr19 + 49177723 49177723 49177723 CCCTTCATCTCCCTTCCCTGCCTGCAAGGATTATCACCCCATTTTGCAGATGAAGAGACTGAGGC CCCTTCATCTCCCTTCCCTGCCTGCAAGGATTTTCACCCCATTTTGCAGATGAAGAGACTGAGGC A T TRPM4 Ensembl:ENSG00000130529 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1189121112 Functional Loss SNV dbSNP153 33..33 33 - - - 15061 RMVar_ID_15061 Human_SNP_ID_668310069 A-to-I Human chr19 - 49313020 49313020 49313020 GGAGTGCAGTCGTGCGATCTCGGCTCATTGCAACCTCCGCCTCCTGTGTTCAAACGATCCTCCTG GGAGTGCAGTCGTGCGATCTCGGCTCATTGCAGCCTCCGCCTCCTGTGTTCAAACGATCCTCCTG T C SLC6A16 Ensembl:ENSG00000063127 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs541335984 Functional Loss SNV dbSNP153 33..33 33 - - - 15062 RMVar_ID_15062 Human_SNP_ID_668314371 A-to-I Human chr19 - 49331302 49331302 49331302 GTGGTATGTACCTACAGTCCCAGCTACTCAGGAGGCTGAGGTGGGAGGACTGCTTGAGCCTGGGA GTGGTATGTACCTACAGTCCCAGCTACTCAGGTGGCTGAGGTGGGAGGACTGCTTGAGCCTGGGA T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1176569438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27470258 15063 RMVar_ID_15063 Human_SNP_ID_668314372 A-to-I Human chr19 - 49331305 49331305 49331305 TTTGTGGTATGTACCTACAGTCCCAGCTACTCAGGAGGCTGAGGTGGGAGGACTGCTTGAGCCTG TTTGTGGTATGTACCTACAGTCCCAGCTACTCGGGAGGCTGAGGTGGGAGGACTGCTTGAGCCTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170150340 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25429996,Human_RBP_ID_27470258 15064 RMVar_ID_15064 Human_SNP_ID_668314651 A-to-I Human chr19 - 49332312 49332312 49332312 GACCTCGTGATCCACCCACTTCAGCTTCCCAAAGTTCTGGGATTACAGGCGTGAGCCACCGCACC GACCTCGTGATCCACCCACTTCAGCTTCCCAATGTTCTGGGATTACAGGCGTGAGCCACCGCACC T A AC011450.1 Ensembl:ENSG00000197813 lincRNA exon GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1458882453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2029446 15065 RMVar_ID_15065 Human_SNP_ID_668349460 A-to-I Human chr19 - 49452508 49452508 49452508 CTCCTGCGTCAGCCTGCACAGTAGCTGGGACTACAGGCAGGTGCCATCAAGCCTGGCTAATTTTT CTCCTGCGTCAGCCTGCACAGTAGCTGGGACTGCAGGCAGGTGCCATCAAGCCTGGCTAATTTTT T C PIH1D1 Ensembl:ENSG00000104872 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs375158251 Functional Loss SNV dbSNP153 33..33 33 - - - 15066 RMVar_ID_15066 Human_SNP_ID_668354920 A-to-I Human chr19 + 49467203 49467202 49467204 GCACACATGACTGGGTGTTTTTGTATTTTTGCAGAGACAAGAGACTCGCCATGTTGCCCAGGCTG GCACACATGACTGGGTGTTTTTGTATTTTTGC__AGACAAGAGACTCGCCATGTTGCCCAGGCTG CAG C ALDH16A1,AC010619.2 Ensembl:ENSG00000161618,Ensembl:ENSG00000269469 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1240609210 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_97239,RMVar_hsa_circ_125592,RMVar_hsa_circ_195846,RMVar_hsa_circ_195847 15067 RMVar_ID_15067 Human_SNP_ID_668354926 A-to-I Human chr19 + 49467221 49467221 49467221 TTTTGTATTTTTGCAGAGACAAGAGACTCGCCATGTTGCCCAGGCTGATCTTGAACTCCTAGCTT TTTTGTATTTTTGCAGAGACAAGAGACTCGCCTTGTTGCCCAGGCTGATCTTGAACTCCTAGCTT A T ALDH16A1,AC010619.2 Ensembl:ENSG00000161618,Ensembl:ENSG00000269469 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1208825116 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97239,RMVar_hsa_circ_125592,RMVar_hsa_circ_195846,RMVar_hsa_circ_195847 15068 RMVar_ID_15068 Human_SNP_ID_668355134 A-to-I Human chr19 + 49467930 49467930 49467930 TAATCTCAGCACTTTGCGAGGCCAAGGTGGGCAGATCACAAGGTCAAGAGATCGAGACCATCCTG TAATCTCAGCACTTTGCGAGGCCAAGGTGGGCGGATCACAAGGTCAAGAGATCGAGACCATCCTG A G ALDH16A1,AC010619.2 Ensembl:ENSG00000161618,Ensembl:ENSG00000269469 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1376094573 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97239,RMVar_hsa_circ_125592,RMVar_hsa_circ_195846,RMVar_hsa_circ_195847 15069 RMVar_ID_15069 Human_SNP_ID_668355136 A-to-I Human chr19 + 49467937 49467937 49467937 AGCACTTTGCGAGGCCAAGGTGGGCAGATCACAAGGTCAAGAGATCGAGACCATCCTGGCTAACA AGCACTTTGCGAGGCCAAGGTGGGCAGATCACGAGGTCAAGAGATCGAGACCATCCTGGCTAACA A G ALDH16A1,AC010619.2 Ensembl:ENSG00000161618,Ensembl:ENSG00000269469 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1465395458 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97239,RMVar_hsa_circ_125592,RMVar_hsa_circ_195846,RMVar_hsa_circ_195847 15070 RMVar_ID_15070 Human_SNP_ID_668356256 A-to-I Human chr19 + 49471252 49471252 49471252 TTTTTTTGGTTTGTTTTTTGTTTTTTCGAGACAGAGTCTCTCTGTCGGCCAGGCTGGAGTGCAGC TTTTTTTGGTTTGTTTTTTGTTTTTTCGAGACGGAGTCTCTCTGTCGGCCAGGCTGGAGTGCAGC A G AC010619.2 Ensembl:ENSG00000269469 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1317591415 Functional Loss SNV dbSNP153 33..33 33 - - - 15071 RMVar_ID_15071 Human_SNP_ID_668361880 A-to-I Human chr19 + 49488906 49488906 49488906 TTTTGTGTTTTTAGTAGAGACAGGGTTTCACCATATTGGCCAGGATGGTCTCGAACTCCTGACCT TTTTGTGTTTTTAGTAGAGACAGGGTTTCACCGTATTGGCCAGGATGGTCTCGAACTCCTGACCT A G RPL13A Ensembl:ENSG00000142541 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1416188193 Functional Loss SNV dbSNP153 33..33 33 - - - 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 15072 RMVar_ID_15072 Human_SNP_ID_668362024 A-to-I Human chr19 + 49489294 49489294 49489294 GAGGCACACGGTTCACTTGAAGCGAGGAGTACAAGAGCAGCCTAGGCAACATGGCAAAACCCTGA GAGGCACACGGTTCACTTGAAGCGAGGAGTACCAGAGCAGCCTAGGCAACATGGCAAAACCCTGA A C RPL13A Ensembl:ENSG00000142541 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474892991 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13495506,Human_RBP_ID_17569078 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 15073 RMVar_ID_15073 Human_SNP_ID_668364027 A-to-I Human chr19 + 49493562 49493562 49493562 AAAATTAGCTGGACGTGGCGCAGGGCGCCTGTAATCCCAGCTAGTCGGGAGGCTGAGGTAGGAGA AAAATTAGCTGGACGTGGCGCAGGGCGCCTGTGATCCCAGCTAGTCGGGAGGCTGAGGTAGGAGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1330313951 Functional Loss SNV dbSNP153 33..33 33 - - - 15074 RMVar_ID_15074 Human_SNP_ID_668365411 A-to-I Human chr19 - 49497010 49497010 49497010 TCTAAGACATGACCACCCTGACCTTACCTGTAATTCATACTCAGATCTAAGCCCGAGGTTATTTC TCTAAGACATGACCACCCTGACCTTACCTGTAGTTCATACTCAGATCTAAGCCCGAGGTTATTTC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs570646138 Functional Loss SNV dbSNP153 33..33 33 - - - 15075 RMVar_ID_15075 Human_SNP_ID_668373163 A-to-I Human chr19 + 49521812 49521812 49521812 CCACCTTACCCTTCCTGAATGGATGGGGCCACAGGTGTGTACCATCACACGTAGTTAATTTTTAA CCACCTTACCCTTCCTGAATGGATGGGGCCACTGGTGTGTACCATCACACGTAGTTAATTTTTAA A T FCGRT Ensembl:ENSG00000104870 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1332902948 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2030869,Human_Splice_Rec_2030925 15076 RMVar_ID_15076 Human_SNP_ID_668385912 A-to-I Human chr19 - 49561702 49561702 49561702 AATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGATCTTGAACTCCTGA AATTTTTGTATTTTTAGTAGAGACGGGGTTTCCCCATGTTGGCCAGGCTGATCTTGAACTCCTGA T G NOSIP Ensembl:ENSG00000142546 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs933010532 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23847,RMVar_hsa_circ_79470,RMVar_hsa_circ_195886 15077 RMVar_ID_15077 Human_SNP_ID_668398832 A-to-I Human chr19 + 49602476 49602476 49602476 ATCTCAGCACTTTGGGAGTTTGAGACCAGCCTAGGCAACATAATGAAACCTTTTCTCTCAAACAA ATCTCAGCACTTTGGGAGTTTGAGACCAGCCTGGGCAACATAATGAAACCTTTTCTCTCAAACAA A G PRR12 Ensembl:ENSG00000126464 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs186878261 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_195887,RMVar_hsa_circ_115272,RMVar_hsa_circ_46183,RMVar_hsa_circ_368010 15078 RMVar_ID_15078 Human_SNP_ID_668399878 A-to-I Human chr19 + 49606140 49606140 49606140 CTCCCACCTCAGCCTCCCAAGTAACTAGGACTACAAGCATACAACACCATGCCTGGCAAATTTTT CTCCCACCTCAGCCTCCCAAGTAACTAGGACTGCAAGCATACAACACCATGCCTGGCAAATTTTT A G PRR12 Ensembl:ENSG00000126464 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs570761473 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_195887,RMVar_hsa_circ_115272,RMVar_hsa_circ_46183,RMVar_hsa_circ_368010 15079 RMVar_ID_15079 Human_SNP_ID_668400360 A-to-I Human chr19 + 49607561 49607561 49607561 AACGCCCCCCCTACAAAAAAATAAGAAAAATTAGCCGGATATAGTGGCATGTGCTTGTTGTCCCA AACGCCCCCCCTACAAAAAAATAAGAAAAATTTGCCGGATATAGTGGCATGTGCTTGTTGTCCCA A T PRR12 Ensembl:ENSG00000126464 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs576775108 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_195887,RMVar_hsa_circ_115272,RMVar_hsa_circ_46183,RMVar_hsa_circ_368010 15080 RMVar_ID_15080 Human_SNP_ID_668400613 A-to-I Human chr19 + 49608510 49608509 49608511 CTCCTGCCTCAGCCTCCCGAGTAGCGCAGACTACAGGCAAGTGCCACCACACCCAGCTAATTTCT CTCCTGCCTCAGCCTCCCGAGTAGCGCAGACT__AGGCAAGTGCCACCACACCCAGCTAATTTCT TAC T PRR12 Ensembl:ENSG00000126464 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1361436461 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_195887,RMVar_hsa_circ_115272,RMVar_hsa_circ_46183,RMVar_hsa_circ_368010 15081 RMVar_ID_15081 Human_SNP_ID_668400614 A-to-I Human chr19 + 49608510 49608510 49608510 CTCCTGCCTCAGCCTCCCGAGTAGCGCAGACTACAGGCAAGTGCCACCACACCCAGCTAATTTCT CTCCTGCCTCAGCCTCCCGAGTAGCGCAGACTGCAGGCAAGTGCCACCACACCCAGCTAATTTCT A G PRR12 Ensembl:ENSG00000126464 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs117038286 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_195887,RMVar_hsa_circ_115272,RMVar_hsa_circ_46183,RMVar_hsa_circ_368010 15082 RMVar_ID_15082 Human_SNP_ID_668400881 A-to-I Human chr19 + 49609436 49609433 49609436 CAGCCTGGACAACATGGTGCAATCCCGTCTCTACTAAGAATACAAAAATTAGCCGGACATGGTGG CAGCCTGGACAACATGGTGCAATCCCGTCT___CTAAGAATACAAAAATTAGCCGGACATGGTGG TCTA T PRR12 Ensembl:ENSG00000126464 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs934449814 Functional Loss DEL dbSNP153 31..33 33 - - - RMVar_hsa_circ_195887,RMVar_hsa_circ_115272,RMVar_hsa_circ_46183,RMVar_hsa_circ_368010 15083 RMVar_ID_15083 Human_SNP_ID_668401425 A-to-I Human chr19 + 49611255 49611255 49611255 AGGTGGCTGAGGCAGGAGGATCACTTGAGCCTAGGAGGCCATAGGTAAGCTATGGTCATGGTTGT AGGTGGCTGAGGCAGGAGGATCACTTGAGCCTTGGAGGCCATAGGTAAGCTATGGTCATGGTTGT A T PRR12 Ensembl:ENSG00000126464 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1478653180 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_195887,RMVar_hsa_circ_115272,RMVar_hsa_circ_46183,RMVar_hsa_circ_368010 15084 RMVar_ID_15084 Human_SNP_ID_668404105 A-to-I Human chr19 + 49619982 49619982 49619982 GGTTCAAGCCGTCCTACCTCAGCCTTCCGAGTAGCTGGGATTACAGGCGTGTGCCACCACGCCTG GGTTCAAGCCGTCCTACCTCAGCCTTCCGAGTGGCTGGGATTACAGGCGTGTGCCACCACGCCTG A G PRR12 Ensembl:ENSG00000126464 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs901314236 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_68727,RMVar_hsa_circ_345556 15085 RMVar_ID_15085 Human_SNP_ID_668407180 A-to-I Human chr19 + 49629079 49629079 49629079 ACAGGCATGAGCCACTGTGCCCAGCCAACCCTATCTCTCTTAAAATTACAGAAATTAGCCAGGCA ACAGGCATGAGCCACTGTGCCCAGCCAACCCTCTCTCTCTTAAAATTACAGAAATTAGCCAGGCA A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs977551059 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17929415 15086 RMVar_ID_15086 Human_SNP_ID_668407181 A-to-I Human chr19 + 49629079 49629079 49629079 ACAGGCATGAGCCACTGTGCCCAGCCAACCCTATCTCTCTTAAAATTACAGAAATTAGCCAGGCA ACAGGCATGAGCCACTGTGCCCAGCCAACCCTGTCTCTCTTAAAATTACAGAAATTAGCCAGGCA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs977551059 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17929415 15087 RMVar_ID_15087 Human_SNP_ID_668418839 A-to-I Human chr19 - 49664705 49664705 49664705 CCGCATCCCTTGGAAGCACGGCCTACGGCAGGATGCACAGCAGGAGGATTTCGGAATCTTCCAGG CCGCATCCCTTGGAAGCACGGCCTACGGCAGGTTGCACAGCAGGAGGATTTCGGAATCTTCCAGG T A IRF3 Ensembl:ENSG00000126456 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1056931602 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1569762,Human_RBP_ID_19090696,Human_RBP_ID_22977510 Human_Splice_Rec_2031309,Human_Splice_Rec_2031321,Human_Splice_Rec_2031341,Human_Splice_Rec_2031355,Human_Splice_Rec_2031369,Human_Splice_Rec_2031383,Human_Splice_Rec_2031397,Human_Splice_Rec_2031465,Human_Splice_Rec_2031479,Human_Splice_Rec_2031515,Human_Splice_Rec_2031531,Human_Splice_Rec_2031537,Human_Splice_Rec_2031543,Human_Splice_Rec_2031557 15088 RMVar_ID_15088 Human_SNP_ID_668419968 A-to-I Human chr19 + 49667960 49667960 49667960 ACGCCAGCATACTAGCTGATTTTTATACTTTTAGTAGACACGGGGTTTCGCCACGTTGGCCAGGC ACGCCAGCATACTAGCTGATTTTTATACTTTTGGTAGACACGGGGTTTCGCCACGTTGGCCAGGC A G BCL2L12 Ensembl:ENSG00000126453 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs911437231 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13496638,Human_RBP_ID_18306581,Human_RBP_ID_23179992 RMVar_hsa_circ_91535,RMVar_hsa_circ_81815,RMVar_hsa_circ_195897,RMVar_hsa_circ_114011,RMVar_hsa_circ_195898,RMVar_hsa_circ_195899 15089 RMVar_ID_15089 Human_SNP_ID_668419993 A-to-I Human chr19 + 49668041 49668041 49668041 GCCTCAAGTGACCCTCCCACGTCGGCCTCCCAAAATGTTGAGATTGCAGACGTGAGCCACCGCAC GCCTCAAGTGACCCTCCCACGTCGGCCTCCCAGAATGTTGAGATTGCAGACGTGAGCCACCGCAC A G BCL2L12 Ensembl:ENSG00000126453 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs906484742 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5190778,Human_RBP_ID_13496640 RMVar_hsa_circ_91535,RMVar_hsa_circ_81815,RMVar_hsa_circ_195897,RMVar_hsa_circ_114011,RMVar_hsa_circ_195898,RMVar_hsa_circ_195899 15090 RMVar_ID_15090 Human_SNP_ID_668420026 A-to-I Human chr19 + 49668120 49668120 49668120 CATTCTTTTTTTTTTTTTTTTTTTTGAGACGGAGTTTCGCCCTTGTTGCCCAGGCTGGAGTGCAA CATTCTTTTTTTTTTTTTTTTTTTTGAGACGGGGTTTCGCCCTTGTTGCCCAGGCTGGAGTGCAA A G BCL2L12 Ensembl:ENSG00000126453 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1441959979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25430598 RMVar_hsa_circ_91535,RMVar_hsa_circ_81815,RMVar_hsa_circ_195897,RMVar_hsa_circ_114011,RMVar_hsa_circ_195898,RMVar_hsa_circ_195899 15091 RMVar_ID_15091 Human_SNP_ID_668421463 A-to-I Human chr19 + 49673006 49673006 49673006 TCCCTGCCTCAGCCTCCTGAGTAGCTGGGGTTACAGGCGCACACCACCATGTCCGGCTAATTTTG TCCCTGCCTCAGCCTCCTGAGTAGCTGGGGTTGCAGGCGCACACCACCATGTCCGGCTAATTTTG A G BCL2L12 Ensembl:ENSG00000126453 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs932067727 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116249,RMVar_hsa_circ_91535,RMVar_hsa_circ_114011,RMVar_hsa_circ_195898,RMVar_hsa_circ_195899,RMVar_hsa_circ_195901,RMVar_hsa_circ_125744,RMVar_hsa_circ_195902 15092 RMVar_ID_15092 Human_SNP_ID_668423920 A-to-I Human chr19 + 49681098 49681098 49681098 TTTAGAGACGGTCTCGCTCTGTCGCCCAGGCTAGAGTGCATTGGTGCAATCATGGCTCACTGCAG TTTAGAGACGGTCTCGCTCTGTCGCCCAGGCTGGAGTGCATTGGTGCAATCATGGCTCACTGCAG A G PRMT1 Ensembl:ENSG00000126457 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs980932681 Functional Loss SNV dbSNP153 33..33 33 - - - 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_195910 15093 RMVar_ID_15093 Human_SNP_ID_668424464 A-to-I Human chr19 + 49682925 49682925 49682925 CTCCTGCCTCAGCCTCCCAATTAGCTGGGATTACAGGCGCCAGCCACCACGCCCGGCTAATTTTT CTCCTGCCTCAGCCTCCCAATTAGCTGGGATTGCAGGCGCCAGCCACCACGCCCGGCTAATTTTT A G PRMT1 Ensembl:ENSG00000126457 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1255655742 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100864,RMVar_hsa_circ_115510,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_342089,RMVar_hsa_circ_107574,RMVar_hsa_circ_96686,RMVar_hsa_circ_195913,RMVar_hsa_circ_374325,RMVar_hsa_circ_195910,RMVar_hsa_circ_195915,RMVar_hsa_circ_79774,RMVar_hsa_circ_195914 15094 RMVar_ID_15094 Human_SNP_ID_668424494 A-to-I Human chr19 + 49682993 49682993 49682993 TTTTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGGTCTCGATCTCCTGACCTCGTGA TTTTTTTAGTAGAGACGGGGTTTCACCGTGTTGGCCAGGATGGTCTCGATCTCCTGACCTCGTGA A G PRMT1 Ensembl:ENSG00000126457 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs566272146 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100864,RMVar_hsa_circ_115510,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_342089,RMVar_hsa_circ_107574,RMVar_hsa_circ_96686,RMVar_hsa_circ_195913,RMVar_hsa_circ_374325,RMVar_hsa_circ_195910,RMVar_hsa_circ_195915,RMVar_hsa_circ_79774,RMVar_hsa_circ_195914 15095 RMVar_ID_15095 Human_SNP_ID_668424629 A-to-I Human chr19 + 49683417 49683417 49683417 ACCCAGTTAAAAACAAAATCGCGGCCGGGCACAGTGGCTCACGCCTGTAATCCCAACATTTTGGG ACCCAGTTAAAAACAAAATCGCGGCCGGGCACTGTGGCTCACGCCTGTAATCCCAACATTTTGGG A T PRMT1 Ensembl:ENSG00000126457 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs967553966 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100864,RMVar_hsa_circ_115510,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_342089,RMVar_hsa_circ_107574,RMVar_hsa_circ_96686,RMVar_hsa_circ_195913,RMVar_hsa_circ_374325,RMVar_hsa_circ_195910,RMVar_hsa_circ_195915,RMVar_hsa_circ_79774,RMVar_hsa_circ_195914 15096 RMVar_ID_15096 Human_SNP_ID_668424667 A-to-I Human chr19 + 49683541 49683541 49683541 ACACCCTGTCTCTACTAAAAATACAAAAAATTAGCCGGACTTGGTGGCTGGCACCTGTAGTCCCA ACACCCTGTCTCTACTAAAAATACAAAAAATTGGCCGGACTTGGTGGCTGGCACCTGTAGTCCCA A G PRMT1 Ensembl:ENSG00000126457 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1256590788 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100864,RMVar_hsa_circ_115510,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_342089,RMVar_hsa_circ_107574,RMVar_hsa_circ_96686,RMVar_hsa_circ_195913,RMVar_hsa_circ_374325,RMVar_hsa_circ_195910,RMVar_hsa_circ_195915,RMVar_hsa_circ_79774,RMVar_hsa_circ_195914 15097 RMVar_ID_15097 Human_SNP_ID_668424681 A-to-I Human chr19 + 49683573 49683573 49683573 AGCCGGACTTGGTGGCTGGCACCTGTAGTCCCAGCTACTCGGGAGGCTGAAGCAGGAGAATGGCG AGCCGGACTTGGTGGCTGGCACCTGTAGTCCCTGCTACTCGGGAGGCTGAAGCAGGAGAATGGCG A T PRMT1 Ensembl:ENSG00000126457 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1440499663 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100864,RMVar_hsa_circ_115510,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_342089,RMVar_hsa_circ_107574,RMVar_hsa_circ_96686,RMVar_hsa_circ_195913,RMVar_hsa_circ_374325,RMVar_hsa_circ_195910,RMVar_hsa_circ_195915,RMVar_hsa_circ_79774,RMVar_hsa_circ_195914 15098 RMVar_ID_15098 Human_SNP_ID_668434099 A-to-I Human chr19 + 49712212 49712212 49712212 TAAAAATACAAAAATTAGCTGGGTATGGTGACAGGCACCTGTAATCCCAGCTACTTGGGAGGGCT TAAAAATACAAAAATTAGCTGGGTATGGTGACGGGCACCTGTAATCCCAGCTACTTGGGAGGGCT A G CPT1C Ensembl:ENSG00000169169 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs968712454 Functional Loss SNV dbSNP153 33..33 33 - - - 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 15099 RMVar_ID_15099 Human_SNP_ID_668459692 A-to-I Human chr19 + 49804129 49804129 49804129 GTAGTGGCACGCGACTGTAATCCCAGCTACTCAGGAGGCTGAGACAGGAGAATCGCTTGAGCCTG GTAGTGGCACGCGACTGTAATCCCAGCTACTCGGGAGGCTGAGACAGGAGAATCGCTTGAGCCTG A G AP2A1 Ensembl:ENSG00000196961 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1263023663 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63805,RMVar_hsa_circ_111802,RMVar_hsa_circ_195941 15100 RMVar_ID_15100 Human_SNP_ID_668465927 A-to-I Human chr19 + 49822535 49822535 49822535 GGTCTCAAGTGATCCTCCACTTCAGTGTCCCTAAGTGCTGGGATTAGAGGCATGAGATGCTGCAC GGTCTCAAGTGATCCTCCACTTCAGTGTCCCTCAGTGCTGGGATTAGAGGCATGAGATGCTGCAC A C MED25 Ensembl:ENSG00000104973 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1045789363 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17567767 15101 RMVar_ID_15101 Human_SNP_ID_668466405 A-to-I Human chr19 + 49824478 49824478 49824478 ATGGTGGTGCACACCTGTAGTCCCAGCTACTCAGGAGGCTGAGGTAGGAGGATCAACTGAGACTG ATGGTGGTGCACACCTGTAGTCCCAGCTACTCGGGAGGCTGAGGTAGGAGGATCAACTGAGACTG A G MED25 Ensembl:ENSG00000104973 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs190637304 Functional Loss SNV dbSNP153 33..33 33 - - - 15102 RMVar_ID_15102 Human_SNP_ID_668472194 A-to-I Human chr19 - 49843388 49843388 49843388 GGTCTGTCTCCCAGGCTGGAGTCAGTGGCACAATCTCTGCTCACTGCAGCCTCTGCCTCCTGGGT GGTCTGTCTCCCAGGCTGGAGTCAGTGGCACAGTCTCTGCTCACTGCAGCCTCTGCCTCCTGGGT T C PTOV1-AS1 Ensembl:ENSG00000268006 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1488765460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13497521 15103 RMVar_ID_15103 Human_SNP_ID_668479499 A-to-I Human chr19 - 49861873 49861873 49861873 GTTTGTGACCTCTCGTGTCCCCAGGACACGCTAGGCTCCTGGCAGCGCTGTGTGACCACGTGTGA GTTTGTGACCTCTCGTGTCCCCAGGACACGCTTGGCTCCTGGCAGCGCTGTGTGACCACGTGTGA T A PNKP Ensembl:ENSG00000039650 Protein coding exon GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1246502129 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_769849,Human_RBP_ID_914660,Human_RBP_ID_3957417,Human_RBP_ID_18995329,Human_RBP_ID_22546272,Human_RBP_ID_22664063,Human_RBP_ID_25441473,Human_RBP_ID_26816242 Human_Splice_Rec_2033146,Human_Splice_Rec_2033168,Human_Splice_Rec_2033196,Human_Splice_Rec_2033226,Human_Splice_Rec_2033288,Human_Splice_Rec_2033296,Human_Splice_Rec_2033322,Human_Splice_Rec_2033352,Human_Splice_Rec_2033382,Human_Splice_Rec_2033402 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 15104 RMVar_ID_15104 Human_SNP_ID_668481575 A-to-I Human chr19 - 49866001 49866001 49866001 CTCAAAAAAAGAAAAGAAAAAATATGGCTGGGAGAGAAGGGGATGTGTCCAGTAAAGAAAGAAGT CTCAAAAAAAGAAAAGAAAAAATATGGCTGGGGGAGAAGGGGATGTGTCCAGTAAAGAAAGAAGT T C PNKP Ensembl:ENSG00000039650 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs994801798 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13497813 RMVar_hsa_circ_113881,RMVar_hsa_circ_195958 15105 RMVar_ID_15105 Human_SNP_ID_668481977 A-to-I Human chr19 - 49867151 49867151 49867151 GGCCGCTTGTGGCTCGAGAGCCCCCCTGGGGGAGCGCCCCCCATCTTCCTGCCCTCGGACGGGCA GGCCGCTTGTGGCTCGAGAGCCCCCCTGGGGGGGCGCCCCCCATCTTCCTGCCCTCGGACGGGCA T C PNKP Ensembl:ENSG00000039650 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs757978147 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_22070457 Human_Splice_Rec_2033175,Human_Splice_Rec_2033203,Human_Splice_Rec_2033234,Human_Splice_Rec_2033235,Human_Splice_Rec_2033264,Human_Splice_Rec_2033265,Human_Splice_Rec_2033301,Human_Splice_Rec_2033329,Human_Splice_Rec_2033360,Human_Splice_Rec_2033361,Human_Splice_Rec_2033452,Human_Splice_Rec_2033453,Human_Splice_Rec_2033466,Human_Splice_Rec_2033467,Human_Splice_Rec_2033477,Human_Splice_Rec_2033486,Human_Splice_Rec_2033487,Human_Splice_Rec_2033496,Human_Splice_Rec_2033497,Human_Splice_Rec_2033499,Human_Splice_Rec_2033502,Human_Splice_Rec_2033503,Human_Splice_Rec_2033506,Human_Splice_Rec_2033510 15106 RMVar_ID_15106 Human_SNP_ID_668482834 A-to-I Human chr19 - 49869597 49869597 49869597 GGGTCAACTCCTTTGTTTTCCGCCTAGCGACAAGGGATTTGCTCGCACGGCATTGGCTCCATCCC GGGTCAACTCCTTTGTTTTCCGCCTAGCGACAGGGGATTTGCTCGCACGGCATTGGCTCCATCCC T C PNKP,AKT1S1 Ensembl:ENSG00000039650,Ensembl:ENSG00000204673 Protein coding,Protein coding intron,3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1159767003 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_240814,Human_RBP_ID_525684,Human_RBP_ID_1569940,Human_RBP_ID_1891064,Human_RBP_ID_5261676,Human_RBP_ID_6779379,Human_RBP_ID_17270295,Human_RBP_ID_17385176,Human_RBP_ID_17501215,Human_RBP_ID_27682037 Human_miRNA_ID_444781,Human_miRNA_ID_544317,Human_miRNA_ID_579554,Human_miRNA_ID_2142651,Human_miRNA_ID_3046460 RMVar_hsa_circ_127542,RMVar_hsa_circ_195962 15107 RMVar_ID_15107 Human_SNP_ID_668497187 A-to-I Human chr19 - 49912722 49912722 49912722 AGCTGCGACTACAGGCGCCTGCCACCACGGCCAACTCATTTTTGTGTTTTTTGTGTAGAGACAGC AGCTGCGACTACAGGCGCCTGCCACCACGGCCCACTCATTTTTGTGTTTTTTGTGTAGAGACAGC T G IL4I1,NUP62,AC011452.2 Ensembl:ENSG00000104951,Ensembl:ENSG00000213024,Ensembl:ENSG00000269179 Protein coding,Protein coding,Protein coding intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1174280826 Functional Loss SNV dbSNP153 33..33 33 - - - 15108 RMVar_ID_15108 Human_SNP_ID_668497925 A-to-I Human chr19 - 49914800 49914800 49914800 GGGAGGCGGAGGTTGTAGTGAGCCAAGATCGCACCACCACACTCCAGCCTGGGTGGCAGAGCAAG GGGAGGCGGAGGTTGTAGTGAGCCAAGATCGCTCCACCACACTCCAGCCTGGGTGGCAGAGCAAG T A IL4I1,NUP62,AC011452.2 Ensembl:ENSG00000104951,Ensembl:ENSG00000213024,Ensembl:ENSG00000269179 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1166635381 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9926204,Human_RBP_ID_25430993 15109 RMVar_ID_15109 Human_SNP_ID_668498752 A-to-I Human chr19 - 49917869 49917869 49917869 CACCACCACACCTGGCTAATTTTTATATTTTTAGTAGAGACGGGGGTTTCACCATGTTGGTCAGC CACCACCACACCTGGCTAATTTTTATATTTTTGGTAGAGACGGGGGTTTCACCATGTTGGTCAGC T C IL4I1,NUP62,AC011452.2 Ensembl:ENSG00000104951,Ensembl:ENSG00000213024,Ensembl:ENSG00000269179 Protein coding,Protein coding,Protein coding intron,intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1448526014 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13498487 15110 RMVar_ID_15110 Human_SNP_ID_668498777 A-to-I Human chr19 - 49917968 49917968 49917968 AGAGTCTCGCTCTGTCACCCAGGCTGGAGTGCAGTAGTGCGATCTCGGCTCACTGCAACCTCCGC AGAGTCTCGCTCTGTCACCCAGGCTGGAGTGCGGTAGTGCGATCTCGGCTCACTGCAACCTCCGC T C IL4I1,NUP62,AC011452.2 Ensembl:ENSG00000104951,Ensembl:ENSG00000213024,Ensembl:ENSG00000269179 Protein coding,Protein coding,Protein coding intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1157231114 Functional Loss SNV dbSNP153 33..33 33 - - - 15111 RMVar_ID_15111 Human_SNP_ID_668498863 A-to-I Human chr19 - 49918222 49918222 49918222 CATCTCTACAAAAAATCGAATATTAGCTGGGCATGGCGGCGTATGCCTGTAGTCCCAGCTAACGG CATCTCTACAAAAAATCGAATATTAGCTGGGCTTGGCGGCGTATGCCTGTAGTCCCAGCTAACGG T A IL4I1,NUP62,AC011452.2 Ensembl:ENSG00000104951,Ensembl:ENSG00000213024,Ensembl:ENSG00000269179 Protein coding,Protein coding,Protein coding intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs903666977 Functional Loss SNV dbSNP153 33..33 33 - - - 15112 RMVar_ID_15112 Human_SNP_ID_668498883 A-to-I Human chr19 - 49918329 49918329 49918329 TGGACGTGGTGGCTCGTGCCTGTAATCTTGGCACTTTGGGAGGCAGAGGTGGGAGGATGGCTTCA TGGACGTGGTGGCTCGTGCCTGTAATCTTGGCGCTTTGGGAGGCAGAGGTGGGAGGATGGCTTCA T C IL4I1,NUP62,AC011452.2 Ensembl:ENSG00000104951,Ensembl:ENSG00000213024,Ensembl:ENSG00000269179 Protein coding,Protein coding,Protein coding intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1040491409 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25431026 15113 RMVar_ID_15113 Human_SNP_ID_668499443 A-to-I Human chr19 - 49920221 49920221 49920221 AAAGTTAGCTGGGTGTGGTGGCACGCGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA AAAGTTAGCTGGGTGTGGTGGCACGCGCCTGTGGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA T C IL4I1,NUP62,AC011452.2 Ensembl:ENSG00000104951,Ensembl:ENSG00000213024,Ensembl:ENSG00000269179 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1032961148 Functional Loss SNV dbSNP153 33..33 33 - - - 15114 RMVar_ID_15114 Human_SNP_ID_668499480 A-to-I Human chr19 - 49920362 49920362 49920362 AAAAGAAACTCCTAGGCCGGGCATGGTGGCTCACGCCTGTAATCCCAGCACCTTGGGAGACCGAG AAAAGAAACTCCTAGGCCGGGCATGGTGGCTCCCGCCTGTAATCCCAGCACCTTGGGAGACCGAG T G IL4I1,NUP62,AC011452.2 Ensembl:ENSG00000104951,Ensembl:ENSG00000213024,Ensembl:ENSG00000269179 Protein coding,Protein coding,Protein coding intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs994813323 Functional Loss SNV dbSNP153 33..33 33 - - - 15115 RMVar_ID_15115 Human_SNP_ID_668500795 A-to-I Human chr19 - 49925045 49925043 49925045 GTTGGTCAGGCTGGTCTCGAACTCCCGAACTCAGGCGATCCACCCGCCTCAGCCTCCCAAAGTGC GTTGGTCAGGCTGGTCTCGAACTCCCGAACTC__GCGATCCACCCGCCTCAGCCTCCCAAAGTGC CCT C IL4I1,NUP62,AC011452.2 Ensembl:ENSG00000104951,Ensembl:ENSG00000213024,Ensembl:ENSG00000269179 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251981613 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_13498740 15116 RMVar_ID_15116 Human_SNP_ID_668500819 A-to-I Human chr19 - 49925105 49925105 49925105 AGGCATGTGTCACCACACATGGCTAATTTTGTATTTTTAGTAGAGACGGGGTTTCTCCATGTTGG AGGCATGTGTCACCACACATGGCTAATTTTGTGTTTTTAGTAGAGACGGGGTTTCTCCATGTTGG T C IL4I1,NUP62,AC011452.2 Ensembl:ENSG00000104951,Ensembl:ENSG00000213024,Ensembl:ENSG00000269179 Protein coding,Protein coding,Protein coding intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1183224482 Functional Loss SNV dbSNP153 33..33 33 - - - 15117 RMVar_ID_15117 Human_SNP_ID_668501078 A-to-I Human chr19 - 49926046 49926046 49926046 CACCATCATGCCTGGCTAATTTTTATATTTTTAGTAGATACAGGGTTTCACCATGTTGGTCAGGC CACCATCATGCCTGGCTAATTTTTATATTTTTGGTAGATACAGGGTTTCACCATGTTGGTCAGGC T C IL4I1,NUP62,AC011452.2 Ensembl:ENSG00000104951,Ensembl:ENSG00000213024,Ensembl:ENSG00000269179 Protein coding,Protein coding,Protein coding intron,intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1423393435 Functional Loss SNV dbSNP153 33..33 33 - - - 15118 RMVar_ID_15118 Human_SNP_ID_668501079 A-to-I Human chr19 - 49926054 49926054 49926054 CAGACATGCACCATCATGCCTGGCTAATTTTTATATTTTTAGTAGATACAGGGTTTCACCATGTT CAGACATGCACCATCATGCCTGGCTAATTTTTGTATTTTTAGTAGATACAGGGTTTCACCATGTT T C IL4I1,NUP62,AC011452.2 Ensembl:ENSG00000104951,Ensembl:ENSG00000213024,Ensembl:ENSG00000269179 Protein coding,Protein coding,Protein coding intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1382860323 Functional Loss SNV dbSNP153 33..33 33 - - - 15119 RMVar_ID_15119 Human_SNP_ID_668501109 A-to-I Human chr19 - 49926171 49926171 49926171 AGAGTCTCGCTCTGTTGCCCAGGCTGGAGTGCAGTGGCACCGTCACAGCTCACTGCAACCACCGC AGAGTCTCGCTCTGTTGCCCAGGCTGGAGTGCTGTGGCACCGTCACAGCTCACTGCAACCACCGC T A IL4I1,NUP62,AC011452.2 Ensembl:ENSG00000104951,Ensembl:ENSG00000213024,Ensembl:ENSG00000269179 Protein coding,Protein coding,Protein coding intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1024307294 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22720509 15120 RMVar_ID_15120 Human_SNP_ID_668501110 A-to-I Human chr19 - 49926171 49926171 49926171 AGAGTCTCGCTCTGTTGCCCAGGCTGGAGTGCAGTGGCACCGTCACAGCTCACTGCAACCACCGC AGAGTCTCGCTCTGTTGCCCAGGCTGGAGTGCGGTGGCACCGTCACAGCTCACTGCAACCACCGC T C IL4I1,NUP62,AC011452.2 Ensembl:ENSG00000104951,Ensembl:ENSG00000213024,Ensembl:ENSG00000269179 Protein coding,Protein coding,Protein coding intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1024307294 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22720509 15121 RMVar_ID_15121 Human_SNP_ID_668501172 A-to-I Human chr19 - 49926313 49926313 49926313 GTTGGCCAGGCTGGTCTTGAACTCCTGACTTCAGGTGATCCACCCACCTCGGCCTCCCAAAATGC GTTGGCCAGGCTGGTCTTGAACTCCTGACTTCCGGTGATCCACCCACCTCGGCCTCCCAAAATGC T G IL4I1,NUP62,AC011452.2 Ensembl:ENSG00000104951,Ensembl:ENSG00000213024,Ensembl:ENSG00000269179 Protein coding,Protein coding,Protein coding intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1226325587 Functional Loss SNV dbSNP153 33..33 33 - - - 15122 RMVar_ID_15122 Human_SNP_ID_668501190 A-to-I Human chr19 - 49926367 49926367 49926367 CACCACCACGCCTGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTTGCCATGTTGGCCAGGC CACCACCACGCCTGGCTAATTTTTGTATTTTTCGTAGAGACGGGGTTTTGCCATGTTGGCCAGGC T G IL4I1,NUP62,AC011452.2 Ensembl:ENSG00000104951,Ensembl:ENSG00000213024,Ensembl:ENSG00000269179 Protein coding,Protein coding,Protein coding intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1488331433 Functional Loss SNV dbSNP153 33..33 33 - - - 15123 RMVar_ID_15123 Human_SNP_ID_668501383 A-to-I Human chr19 - 49926976 49926976 49926976 TTGCACCTGTGGTCCCAGCTACTCATGAGGCTAAGGCAGGAGGATCACTTGAACCCTGGGGTGGG TTGCACCTGTGGTCCCAGCTACTCATGAGGCTGAGGCAGGAGGATCACTTGAACCCTGGGGTGGG T C IL4I1,NUP62,AC011452.2 Ensembl:ENSG00000104951,Ensembl:ENSG00000213024,Ensembl:ENSG00000269179 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1359547165 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13498817,Human_RBP_ID_22720510 15124 RMVar_ID_15124 Human_SNP_ID_668508031 A-to-I Human chr19 - 49949168 49949168 49949168 CCTGGGCAAGATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCCGGGCATGGTGGCGG CCTGGGCAAGATGGTGAAACCCCATCTCTACTGAAAATACAAAAATTAGCCGGGCATGGTGGCGG T C SIGLEC11,AC011452.2 Ensembl:ENSG00000161640,Ensembl:ENSG00000269179 Protein coding,Protein coding 3'UTR,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1159114788 Functional Loss SNV dbSNP153 33..33 33 - - - 15125 RMVar_ID_15125 Human_SNP_ID_668527915 A-to-I Human chr19 - 50014483 50014483 50014483 AACATCTCGGCTCACTGCAACCTCCGTCTCCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCA AACATCTCGGCTCACTGCAACCTCCGTCTCCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCA T C VRK3 Ensembl:ENSG00000105053 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1487157616 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51254,RMVar_hsa_circ_78705,RMVar_hsa_circ_195981,RMVar_hsa_circ_40257 15126 RMVar_ID_15126 Human_SNP_ID_668531469 A-to-I Human chr19 + 50026300 50026300 50026300 GTTATGAAAACCGCTCAAGGTCTGGGCACGGTAGATCACGCCTGTAATCCCAGCACTTTGGGAAG GTTATGAAAACCGCTCAAGGTCTGGGCACGGTGGATCACGCCTGTAATCCCAGCACTTTGGGAAG A G ZNF473 Ensembl:ENSG00000142528 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs8108728 Functional Loss SNV dbSNP153 33..33 33 - - - 15127 RMVar_ID_15127 Human_SNP_ID_668531504 A-to-I Human chr19 + 50026397 50026397 50026397 TTCCTCGAACCCCCAGTCTCTACTAAAAATACAAAAATTAGTTGAGCGTGGTGGCGGGGGCCTGT TTCCTCGAACCCCCAGTCTCTACTAAAAATACTAAAATTAGTTGAGCGTGGTGGCGGGGGCCTGT A T ZNF473 Ensembl:ENSG00000142528 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1410305664 Functional Loss SNV dbSNP153 33..33 33 - - - 15128 RMVar_ID_15128 Human_SNP_ID_668580710 A-to-I Human chr19 + 50235265 50235265 50235265 CTGTAGTCCCAGCTACTCAGGAGGCTGAGGCTAGAGAATTGCTTGAACCTGGGAGGCAGAGGTTG CTGTAGTCCCAGCTACTCAGGAGGCTGAGGCTGGAGAATTGCTTGAACCTGGGAGGCAGAGGTTG A G MYH14 Ensembl:ENSG00000105357 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs916868761 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67328,RMVar_hsa_circ_195982,RMVar_hsa_circ_126737,RMVar_hsa_circ_54847,RMVar_hsa_circ_67622,RMVar_hsa_circ_357068,RMVar_hsa_circ_122340,RMVar_hsa_circ_195985 15129 RMVar_ID_15129 Human_SNP_ID_668623112 A-to-I Human chr19 + 50386376 50386376 50386376 CCCAGACTGGTCTCGAATCCCTGACCTCAAGTAATCCTCCCACCTCGGCCTCCCAAAGTGCTGGG CCCAGACTGGTCTCGAATCCCTGACCTCAAGTTATCCTCCCACCTCGGCCTCCCAAAGTGCTGGG A T POLD1 Ensembl:ENSG00000062822 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1261818828 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76877,RMVar_hsa_circ_195992 15130 RMVar_ID_15130 Human_SNP_ID_668626603 A-to-I Human chr19 + 50397664 50397664 50397664 TGACCTCGTGATCCGCCCACCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCATCACAC TGACCTCGTGATCCGCCCACCTTGGCCTCCCACAGTGCTGGGATTACAGGCGTGAGCCATCACAC A C POLD1 Ensembl:ENSG00000062822 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904552757 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76877,RMVar_hsa_circ_195992 15131 RMVar_ID_15131 Human_SNP_ID_668632220 A-to-I Human chr19 + 50412790 50412790 50412790 TTAGTTTTGTGTGTGTGTGTGTGTGTATTTTTAGTAGAGATGGTGTTTCACCATGTTGTCCAGGC TTAGTTTTGTGTGTGTGTGTGTGTGTATTTTTGGTAGAGATGGTGTTTCACCATGTTGTCCAGGC A G POLD1 Ensembl:ENSG00000062822 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1486103388 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23805229 RMVar_hsa_circ_100166,RMVar_hsa_circ_195997,RMVar_hsa_circ_75880,RMVar_hsa_circ_195999,RMVar_hsa_circ_122704,RMVar_hsa_circ_196001 15132 RMVar_ID_15132 Human_SNP_ID_668636452 A-to-I Human chr19 + 50424638 50424638 50424638 CCTCACATTTACTAAAAATACAAAAATTAGCTAGGCGTGGTGGTGTGCACCTGTAGTCCCAGCTA CCTCACATTTACTAAAAATACAAAAATTAGCTGGGCGTGGTGGTGTGCACCTGTAGTCCCAGCTA A G AC020909.1,SPIB Ensembl:ENSG00000142539,Ensembl:ENSG00000269404 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs541136664 Functional Loss SNV dbSNP153 33..33 33 - - - 15133 RMVar_ID_15133 Human_SNP_ID_668636693 A-to-I Human chr19 + 50425580 50425580 50425580 CTCCTGCCTCAGCCTCCTGAGTAGCTAGGACCACAGGCGTACACCACCACACCTGACTAATTTTT CTCCTGCCTCAGCCTCCTGAGTAGCTAGGACCCCAGGCGTACACCACCACACCTGACTAATTTTT A C AC020909.1,SPIB Ensembl:ENSG00000142539,Ensembl:ENSG00000269404 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs755444561 Functional Loss SNV dbSNP153 33..33 33 - - - 15134 RMVar_ID_15134 Human_SNP_ID_668637021 A-to-I Human chr19 + 50426928 50426928 50426928 GAGGTGGGAGGATCACCTGAGGCCAGGAGTTCAAGACCAGCCTGGGCAACATAGTAAGACACCAT GAGGTGGGAGGATCACCTGAGGCCAGGAGTTCGAGACCAGCCTGGGCAACATAGTAAGACACCAT A G AC020909.1,SPIB Ensembl:ENSG00000142539,Ensembl:ENSG00000269404 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs947812948 Functional Loss SNV dbSNP153 33..33 33 - - - 15135 RMVar_ID_15135 Human_SNP_ID_668748774 A-to-I Human chr19 - 50800508 50800508 50800508 TTGATCTCCTGTCCTCGTGATCCACCCGCCTCAGCCTCCCAAAGTGCTGGGATTACACGCGTGAG TTGATCTCCTGTCCTCGTGATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTACACGCGTGAG T C C19orf48 Ensembl:ENSG00000167747 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1371808448 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3479,RMVar_hsa_circ_95887,RMVar_hsa_circ_196019 15136 RMVar_ID_15136 Human_SNP_ID_668749285 A-to-I Human chr19 - 50801737 50801737 50801737 ACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAACCCGTGAGGCAGAGGTTGCAGTGAGCCGAGAT ACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAGCCCGTGAGGCAGAGGTTGCAGTGAGCCGAGAT T C C19orf48 Ensembl:ENSG00000167747 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1359689425 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3479,RMVar_hsa_circ_95887,RMVar_hsa_circ_196019 15137 RMVar_ID_15137 Human_SNP_ID_668749386 A-to-I Human chr19 - 50802059 50802059 50802059 CAAAAACCATCTCAGGCTGGGCGCAGTGGCTTACACCTGTAATTCCAGCACTTTGGGAGGCTGAG CAAAAACCATCTCAGGCTGGGCGCAGTGGCTTGCACCTGTAATTCCAGCACTTTGGGAGGCTGAG T C C19orf48 Ensembl:ENSG00000167747 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1385972210 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22811984 RMVar_hsa_circ_3479,RMVar_hsa_circ_95887,RMVar_hsa_circ_196019 15138 RMVar_ID_15138 Human_SNP_ID_668749565 A-to-I Human chr19 - 50802540 50802540 50802540 TGACTTCGTGATCTGCCCACCTCGGCTTCCCAAAGTGCTGAGGTTGCAGGCGTGAGCCACCGTGC TGACTTCGTGATCTGCCCACCTCGGCTTCCCACAGTGCTGAGGTTGCAGGCGTGAGCCACCGTGC T G C19orf48 Ensembl:ENSG00000167747 Protein coding exon GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs1321025750 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8256333 Human_Splice_Rec_2036536,Human_Splice_Rec_2036537,Human_Splice_Rec_2036556,Human_Splice_Rec_2036557,Human_Splice_Rec_2036574,Human_Splice_Rec_2036575,Human_Splice_Rec_2036599,Human_Splice_Rec_2036608,Human_Splice_Rec_2036609 RMVar_hsa_circ_101969,RMVar_hsa_circ_196020 15139 RMVar_ID_15139 Human_SNP_ID_668749585 A-to-I Human chr19 - 50802597 50802597 50802597 TTGTATTTTCAATAGAGACAGGGTTTCACCATATTGGCCAGGCTGGTCTCGAACTCCTGACTTCG TTGTATTTTCAATAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACTTCG T C C19orf48 Ensembl:ENSG00000167747 Protein coding exon GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,31158229,31158229,31158229 RNA-Seq:(High) rs1488810101 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4544521 Human_Splice_Rec_2036536,Human_Splice_Rec_2036556,Human_Splice_Rec_2036574,Human_Splice_Rec_2036608 RMVar_hsa_circ_101969,RMVar_hsa_circ_196020 15140 RMVar_ID_15140 Human_SNP_ID_668749868 A-to-I Human chr19 - 50803461 50803461 50803461 GAGGTGGGTGGGTCGCTTGACCCTAGGAGTTCAAGACCAGCCTGAGCAACATGGCAAAACCCCAT GAGGTGGGTGGGTCGCTTGACCCTAGGAGTTCGAGACCAGCCTGAGCAACATGGCAAAACCCCAT T C C19orf48 Ensembl:ENSG00000167747 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1350297441 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25431591 15141 RMVar_ID_15141 Human_SNP_ID_668749908 A-to-I Human chr19 - 50803550 50803546 50803550 TCAAAAACCTTGTGCTTAAGTGTTTTGAAAGTAAGTTTCATGGCCGAACGCGGTGGCTCATGCCT TCAAAAACCTTGTGCTTAAGTGTTTTGAAAGT____TTCATGGCCGAACGCGGTGGCTCATGCCT AACTT A C19orf48 Ensembl:ENSG00000167747 Protein coding intron GSE38233;GSE105773 cultured B-cells;Glioblastoma cells,U87MG - 24183664,29724793 RNA-Seq:(High) rs1343893353 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_23180110 15142 RMVar_ID_15142 Human_SNP_ID_668896403 A-to-I Human chr19 - 51348244 51348244 51348244 ACCTGGATAATTTTTGTATTTTTAGTAGAGACAGGGTTTCGCCATGTTGGCCAGGCTGGTCTTGA ACCTGGATAATTTTTGTATTTTTAGTAGAGACGGGGTTTCGCCATGTTGGCCAGGCTGGTCTTGA T C ETFB Ensembl:ENSG00000105379 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1002017690 Functional Loss SNV dbSNP153 33..33 33 - - - 15143 RMVar_ID_15143 Human_SNP_ID_668899868 A-to-I Human chr19 - 51360966 51360966 51360966 CCTGGCTAACACGGTGAGACCTTGTCTCTACTAAAAATACAAAAAATTAGCCAGGCGTGGTGGCA CCTGGCTAACACGGTGAGACCTTGTCTCTACTGAAAATACAAAAAATTAGCCAGGCGTGGTGGCA T C ETFB,AC008750.8 Ensembl:ENSG00000105379,Ensembl:ENSG00000269403 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs777750447 Functional Loss SNV dbSNP153 33..33 33 - - - 15144 RMVar_ID_15144 Human_SNP_ID_668899954 A-to-I Human chr19 - 51361346 51361344 51361346 CCTTGGCTGTCCTGCTTGCTGAGTGCCCTAGCACGTGCCCAGGGACTCGCTTGACAGAAAAGCCT CCTTGGCTGTCCTGCTTGCTGAGTGCCCTAGCGCATGCCCAGGGACTCGCTTGACAGAAAAGCCT CGT TGC ETFB,AC008750.8 Ensembl:ENSG00000105379,Ensembl:ENSG00000269403 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs386810332 Functional Loss MNV dbSNP153 33..35 33 - - - 15145 RMVar_ID_15145 Human_SNP_ID_668899957 A-to-I Human chr19 - 51361346 51361346 51361346 CCTTGGCTGTCCTGCTTGCTGAGTGCCCTAGCACGTGCCCAGGGACTCGCTTGACAGAAAAGCCT CCTTGGCTGTCCTGCTTGCTGAGTGCCCTAGCGCGTGCCCAGGGACTCGCTTGACAGAAAAGCCT T C ETFB,AC008750.8 Ensembl:ENSG00000105379,Ensembl:ENSG00000269403 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4802790 Functional Loss SNV dbSNP153 33..33 33 - - - 15146 RMVar_ID_15146 Human_SNP_ID_668899958 A-to-I Human chr19 - 51361346 51361346 51361347 CCTTGGCTGTCCTGCTTGCTGAGTGCCCTAGCACGTGCCCAGGGACTCGCTTGACAGAAAAGCCT CCTTGGCTGTCCTGCTTGCTGAGTGCCCTAGTGCGTGCCCAGGGACTCGCTTGACAGAAAAGCCT TG CA ETFB,AC008750.8 Ensembl:ENSG00000105379,Ensembl:ENSG00000269403 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs386810333 Functional Loss MNV dbSNP153 32..33 33 - - - 15147 RMVar_ID_15147 Human_SNP_ID_668900292 A-to-I Human chr19 - 51362321 51362321 51362321 CACCCGCCTCAGCCTCCCAACGTGCTGGGATTACAGGTGTGAGCCACTGTGACCAGCTGCAATAA CACCCGCCTCAGCCTCCCAACGTGCTGGGATTGCAGGTGTGAGCCACTGTGACCAGCTGCAATAA T C ETFB,AC008750.8,AC008750.5 Ensembl:ENSG00000105379,Ensembl:ENSG00000269403,Ensembl:ENSG00000268520 Protein coding,Protein coding,lincRNA intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1166405934 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23805622 15148 RMVar_ID_15148 Human_SNP_ID_668900321 A-to-I Human chr19 - 51362443 51362443 51362443 CTCCTGAGTAGCTGGGATTACACGTGTGAGCCACCACGCCTGGCTAATTTTTGTATTTTTAGTAG CTCCTGAGTAGCTGGGATTACACGTGTGAGCCCCCACGCCTGGCTAATTTTTGTATTTTTAGTAG T G ETFB,AC008750.8,AC008750.5 Ensembl:ENSG00000105379,Ensembl:ENSG00000269403,Ensembl:ENSG00000268520 Protein coding,Protein coding,lincRNA intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs891293104 Functional Loss SNV dbSNP153 33..33 33 - - - 15149 RMVar_ID_15149 Human_SNP_ID_668900336 A-to-I Human chr19 - 51362523 51362523 51362523 TTGCCCAGGCTGGAGTGCAGTGGCATGATCTCAGCTCACTGGAACCTCCACTTCCCAGGTTCAAG TTGCCCAGGCTGGAGTGCAGTGGCATGATCTCCGCTCACTGGAACCTCCACTTCCCAGGTTCAAG T G ETFB,AC008750.8,AC008750.5 Ensembl:ENSG00000105379,Ensembl:ENSG00000269403,Ensembl:ENSG00000268520 Protein coding,Protein coding,lincRNA intron,intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1458423312 Functional Loss SNV dbSNP153 33..33 33 - - - 15150 RMVar_ID_15150 Human_SNP_ID_668901205 A-to-I Human chr19 - 51366329 51366329 51366329 TGCGGGCTGACCCTGTAAGTGGCTGCGGCGGGAAGATGGCGGAGCTGCGCGTGCTCGTAGCTGTC TGCGGGCTGACCCTGTAAGTGGCTGCGGCGGGGAGATGGCGGAGCTGCGCGTGCTCGTAGCTGTC T C ETFB,AC008750.8 Ensembl:ENSG00000105379,Ensembl:ENSG00000269403 Protein coding,Protein coding 5'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs776277833 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241372,Human_RBP_ID_526004,Human_RBP_ID_4558709,Human_RBP_ID_5320552,Human_RBP_ID_5421792,Human_RBP_ID_9329168,Human_RBP_ID_9381345,Human_RBP_ID_17935082,Human_RBP_ID_18421674,Human_RBP_ID_22448991 Human_Splice_Rec_2037911,Human_Splice_Rec_2037921,Human_Splice_Rec_2037929 15151 RMVar_ID_15151 Human_SNP_ID_668924974 A-to-I Human chr19 - 51453579 51453579 51453579 GCAATTCTCCTGCCTCAGCCTCCCAAGTAGCCAGGATTACAGGCACGCGCCACCAAGCCAGGCTA GCAATTCTCCTGCCTCAGCCTCCCAAGTAGCCGGGATTACAGGCACGCGCCACCAAGCCAGGCTA T C SIGLEC8 Ensembl:ENSG00000105366 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1198979376 Functional Loss SNV dbSNP153 33..33 33 - - - 15152 RMVar_ID_15152 Human_SNP_ID_668990268 A-to-I Human chr19 + 51696471 51696471 51696471 AAGGGGTGATAGTTTTTTTGTTTTTTTGAGATAGGGTCTCACTTTGTCACCCAGGCTGGATTGCA AAGGGGTGATAGTTTTTTTGTTTTTTTGAGATGGGGTCTCACTTTGTCACCCAGGCTGGATTGCA A G SPACA6 Ensembl:ENSG00000182310 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1164505357 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5191774,Human_RBP_ID_5320565 RMVar_hsa_circ_11725 15153 RMVar_ID_15153 Human_SNP_ID_668990319 A-to-I Human chr19 + 51696723 51696723 51696723 TTCCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAACTACCGTACCTGGCTGGGTGAT TTCCCACCTCAGCCTCCCAAAGTGCTGGGATTCCAGGCATGAACTACCGTACCTGGCTGGGTGAT A C SPACA6 Ensembl:ENSG00000182310 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs907228239 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11725 15154 RMVar_ID_15154 Human_SNP_ID_668990892 A-to-I Human chr19 + 51699243 51699243 51699243 GTTGCCCAGGCTTGTCTCGAACTCCTGGCCTCAAGTGATCCTGTCACCTCAGCCTCCCGAGTAGC GTTGCCCAGGCTTGTCTCGAACTCCTGGCCTCGAGTGATCCTGTCACCTCAGCCTCCCGAGTAGC A G SPACA6 Ensembl:ENSG00000182310 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1198087425 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11725 15155 RMVar_ID_15155 Human_SNP_ID_669051763 A-to-I Human chr19 - 51945545 51945545 51945545 TCCTGTATGAGATCACGTGTATGTGATAAGCTATGACTCTCTGAGCAAGGATTTTCCAATTTGAC TCCTGTATGAGATCACGTGTATGTGATAAGCTGTGACTCTCTGAGCAAGGATTTTCCAATTTGAC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1487815971 Functional Loss SNV dbSNP153 33..33 33 - - - 15156 RMVar_ID_15156 Human_SNP_ID_669064632 A-to-I Human chr19 - 51997061 51997061 51997061 TCTTTGCCTCACCCTACCAAAGTGCTGGGATTACAGACATGAACCACCACACCAGGACATGATTA TCTTTGCCTCACCCTACCAAAGTGCTGGGATTGCAGACATGAACCACCACACCAGGACATGATTA T C ZNF615 Ensembl:ENSG00000197619 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223855725 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196057,RMVar_hsa_circ_120306 15157 RMVar_ID_15157 Human_SNP_ID_669073027 A-to-I Human chr19 - 52031806 52031806 52031806 TTTAGTAGAGACGGGGTTTCACTGTGTTGGCCAGGCTGGCCTTGAACTCTCGACCCCGGGCGGTC TTTAGTAGAGACGGGGTTTCACTGTGTTGGCCGGGCTGGCCTTGAACTCTCGACCCCGGGCGGTC T C ZNF432 Ensembl:ENSG00000256087 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027312772 Functional Loss SNV dbSNP153 33..33 33 - - - 15158 RMVar_ID_15158 Human_SNP_ID_669073051 A-to-I Human chr19 - 52031889 52031889 52031889 GGTTCAAGAGATTTTCCTGCCTCAGCCTCCTAAGTAGCTGGGATTACAGGCACCCACGACCACGC GGTTCAAGAGATTTTCCTGCCTCAGCCTCCTACGTAGCTGGGATTACAGGCACCCACGACCACGC T G ZNF432 Ensembl:ENSG00000256087 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1272527137 Functional Loss SNV dbSNP153 33..33 33 - - - 15159 RMVar_ID_15159 Human_SNP_ID_669073070 A-to-I Human chr19 - 52031956 52031956 52031956 TTCTGCTCTTGTTGCCCAGGTTGGAGTGTAATAGCACGATCTTGGCTCACTGCAACCCCGCCTCC TTCTGCTCTTGTTGCCCAGGTTGGAGTGTAATGGCACGATCTTGGCTCACTGCAACCCCGCCTCC T C ZNF432 Ensembl:ENSG00000256087 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1289873063 Functional Loss SNV dbSNP153 33..33 33 - - - 15160 RMVar_ID_15160 Human_SNP_ID_669073198 A-to-I Human chr19 - 52032484 52032484 52032484 TTCAGTGAGCCAAGATTGCGCCATTGCATTCCAGCCTGGGCAACAAGAGCGAAACTCTGCCTCAA TTCAGTGAGCCAAGATTGCGCCATTGCATTCCCGCCTGGGCAACAAGAGCGAAACTCTGCCTCAA T G ZNF432 Ensembl:ENSG00000256087 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs573420913 Functional Loss SNV dbSNP153 33..33 33 - - - 15161 RMVar_ID_15161 Human_SNP_ID_669073202 A-to-I Human chr19 - 52032494 52032494 52032494 AGGCAGAGGTTTCAGTGAGCCAAGATTGCGCCATTGCATTCCAGCCTGGGCAACAAGAGCGAAAC AGGCAGAGGTTTCAGTGAGCCAAGATTGCGCCGTTGCATTCCAGCCTGGGCAACAAGAGCGAAAC T C ZNF432 Ensembl:ENSG00000256087 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941276803 Functional Loss SNV dbSNP153 33..33 33 - - - 15162 RMVar_ID_15162 Human_SNP_ID_669073236 A-to-I Human chr19 - 52032612 52032612 52032612 GACCAACATGGTGAAGCCCCCCTCTCTACTAAAAATACAAAATTAGCCGAGCATGGTGGCTCACG GACCAACATGGTGAAGCCCCCCTCTCTACTAACAATACAAAATTAGCCGAGCATGGTGGCTCACG T G ZNF432 Ensembl:ENSG00000256087 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1388738514 Functional Loss SNV dbSNP153 33..33 33 - - - 15163 RMVar_ID_15163 Human_SNP_ID_669073237 A-to-I Human chr19 - 52032614 52032614 52032614 CTGACCAACATGGTGAAGCCCCCCTCTCTACTAAAAATACAAAATTAGCCGAGCATGGTGGCTCA CTGACCAACATGGTGAAGCCCCCCTCTCTACTGAAAATACAAAATTAGCCGAGCATGGTGGCTCA T C ZNF432 Ensembl:ENSG00000256087 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1390091263 Functional Loss SNV dbSNP153 33..33 33 - - - 15164 RMVar_ID_15164 Human_SNP_ID_669073238 A-to-I Human chr19 - 52032614 52032614 52032614 CTGACCAACATGGTGAAGCCCCCCTCTCTACTAAAAATACAAAATTAGCCGAGCATGGTGGCTCA CTGACCAACATGGTGAAGCCCCCCTCTCTACTCAAAATACAAAATTAGCCGAGCATGGTGGCTCA T G ZNF432 Ensembl:ENSG00000256087 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1390091263 Functional Loss SNV dbSNP153 33..33 33 - - - 15165 RMVar_ID_15165 Human_SNP_ID_669079948 A-to-I Human chr19 - 52057949 52057949 52057949 CGGTTCACTGTAACCTCTGCCTACCGGGTTCAAGCGATTCTTATGCCTCAGCCTCTTGAGTAGTT CGGTTCACTGTAACCTCTGCCTACCGGGTTCAGGCGATTCTTATGCCTCAGCCTCTTGAGTAGTT T C ZNF432 Ensembl:ENSG00000256087 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1034762624 Functional Loss SNV dbSNP153 33..33 33 - - - 15166 RMVar_ID_15166 Human_SNP_ID_669080243 A-to-I Human chr19 - 52059228 52059228 52059228 CTCCTGCCTCAGCCTCCCAAGTCGCTGGGACTATAGGCGCCCACCACCACGCCTGGCTAATTTTT CTCCTGCCTCAGCCTCCCAAGTCGCTGGGACTGTAGGCGCCCACCACCACGCCTGGCTAATTTTT T C ZNF432,AC011468.1 Ensembl:ENSG00000256087,Ensembl:ENSG00000260160 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025001740 Functional Loss SNV dbSNP153 33..33 33 - - - 15167 RMVar_ID_15167 Human_SNP_ID_669080487 A-to-I Human chr19 - 52059648 52059648 52059648 CACCATGCCTGGCTAATTTTTGTATTTTTTGTAGAGATGAGGTTTCGTCATGTTGCCCAGACTGG CACCATGCCTGGCTAATTTTTGTATTTTTTGTGGAGATGAGGTTTCGTCATGTTGCCCAGACTGG T C ZNF432,AC011468.1 Ensembl:ENSG00000256087,Ensembl:ENSG00000260160 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1246303165 Functional Loss SNV dbSNP153 33..33 33 - - - 15168 RMVar_ID_15168 Human_SNP_ID_669081822 A-to-I Human chr19 - 52064710 52064710 52064710 AGAATTGCTTGAACCCTGGAGGCGGAGGTTGCAGTGAGCCGAGATCGCGCCACTGCACTCTAGCC AGAATTGCTTGAACCCTGGAGGCGGAGGTTGCCGTGAGCCGAGATCGCGCCACTGCACTCTAGCC T G ZNF841,ZNF432 Ensembl:ENSG00000197608,Ensembl:ENSG00000256087 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1442751528 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196065,RMVar_hsa_circ_120820,RMVar_hsa_circ_106922,RMVar_hsa_circ_356345,RMVar_hsa_circ_196064,RMVar_hsa_circ_341674 15169 RMVar_ID_15169 Human_SNP_ID_669081831 A-to-I Human chr19 - 52064762 52064762 52064762 GGGCTTCGTGGCGGGTACTGGTAGTACCAGCTACTCGAGAGGCTGAGTCAGGAGAATTGCTTGAA GGGCTTCGTGGCGGGTACTGGTAGTACCAGCTGCTCGAGAGGCTGAGTCAGGAGAATTGCTTGAA T C ZNF841,ZNF432 Ensembl:ENSG00000197608,Ensembl:ENSG00000256087 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs575564461 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196065,RMVar_hsa_circ_120820,RMVar_hsa_circ_106922,RMVar_hsa_circ_356345,RMVar_hsa_circ_196064,RMVar_hsa_circ_341674 15170 RMVar_ID_15170 Human_SNP_ID_669081832 A-to-I Human chr19 - 52064762 52064762 52064762 GGGCTTCGTGGCGGGTACTGGTAGTACCAGCTACTCGAGAGGCTGAGTCAGGAGAATTGCTTGAA GGGCTTCGTGGCGGGTACTGGTAGTACCAGCTCCTCGAGAGGCTGAGTCAGGAGAATTGCTTGAA T G ZNF841,ZNF432 Ensembl:ENSG00000197608,Ensembl:ENSG00000256087 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs575564461 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196065,RMVar_hsa_circ_120820,RMVar_hsa_circ_106922,RMVar_hsa_circ_356345,RMVar_hsa_circ_196064,RMVar_hsa_circ_341674 15171 RMVar_ID_15171 Human_SNP_ID_669081834 A-to-I Human chr19 - 52064772 52064772 52064772 AAAATTAGCTGGGCTTCGTGGCGGGTACTGGTAGTACCAGCTACTCGAGAGGCTGAGTCAGGAGA AAAATTAGCTGGGCTTCGTGGCGGGTACTGGTGGTACCAGCTACTCGAGAGGCTGAGTCAGGAGA T C ZNF841,ZNF432 Ensembl:ENSG00000197608,Ensembl:ENSG00000256087 Protein coding,Protein coding 3'UTR,intron GSE38233;GSE100210;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 24183664,29129909,30559470 RNA-Seq:(High) rs939022436 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196065,RMVar_hsa_circ_120820,RMVar_hsa_circ_106922,RMVar_hsa_circ_356345,RMVar_hsa_circ_196064,RMVar_hsa_circ_341674 15172 RMVar_ID_15172 Human_SNP_ID_669081842 A-to-I Human chr19 - 52064798 52064798 52064798 GAAACCCTGTTTCTGCCAAAAATACAAAAATTAGCTGGGCTTCGTGGCGGGTACTGGTAGTACCA GAAACCCTGTTTCTGCCAAAAATACAAAAATTGGCTGGGCTTCGTGGCGGGTACTGGTAGTACCA T C ZNF841,ZNF432 Ensembl:ENSG00000197608,Ensembl:ENSG00000256087 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs117555655 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196065,RMVar_hsa_circ_120820,RMVar_hsa_circ_106922,RMVar_hsa_circ_356345,RMVar_hsa_circ_196064,RMVar_hsa_circ_341674 15173 RMVar_ID_15173 Human_SNP_ID_669081844 A-to-I Human chr19 - 52064807 52064807 52064807 CAACATGGTGAAACCCTGTTTCTGCCAAAAATACAAAAATTAGCTGGGCTTCGTGGCGGGTACTG CAACATGGTGAAACCCTGTTTCTGCCAAAAATGCAAAAATTAGCTGGGCTTCGTGGCGGGTACTG T C ZNF841,ZNF432 Ensembl:ENSG00000197608,Ensembl:ENSG00000256087 Protein coding,Protein coding 3'UTR,intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs903718580 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196065,RMVar_hsa_circ_120820,RMVar_hsa_circ_106922,RMVar_hsa_circ_356345,RMVar_hsa_circ_196064,RMVar_hsa_circ_341674 15174 RMVar_ID_15174 Human_SNP_ID_669081845 A-to-I Human chr19 - 52064809 52064809 52064809 GCCAACATGGTGAAACCCTGTTTCTGCCAAAAATACAAAAATTAGCTGGGCTTCGTGGCGGGTAC GCCAACATGGTGAAACCCTGTTTCTGCCAAAAGTACAAAAATTAGCTGGGCTTCGTGGCGGGTAC T C ZNF841,ZNF432 Ensembl:ENSG00000197608,Ensembl:ENSG00000256087 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348274587 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196065,RMVar_hsa_circ_120820,RMVar_hsa_circ_106922,RMVar_hsa_circ_356345,RMVar_hsa_circ_196064,RMVar_hsa_circ_341674 15175 RMVar_ID_15175 Human_SNP_ID_669081847 A-to-I Human chr19 - 52064827 52064827 52064827 GAGTTCAAGAGCAGCCTGGCCAACATGGTGAAACCCTGTTTCTGCCAAAAATACAAAAATTAGCT GAGTTCAAGAGCAGCCTGGCCAACATGGTGAACCCCTGTTTCTGCCAAAAATACAAAAATTAGCT T G ZNF841,ZNF432 Ensembl:ENSG00000197608,Ensembl:ENSG00000256087 Protein coding,Protein coding 3'UTR,intron GSE47997;GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 23474544,29129909,31158229 RNA-Seq:(High) rs935258650 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196065,RMVar_hsa_circ_120820,RMVar_hsa_circ_106922,RMVar_hsa_circ_356345,RMVar_hsa_circ_196064,RMVar_hsa_circ_341674 15176 RMVar_ID_15176 Human_SNP_ID_669081853 A-to-I Human chr19 - 52064853 52064853 52064853 GAGGTGGGCGGATCACTTGAGGTCAGGAGTTCAAGAGCAGCCTGGCCAACATGGTGAAACCCTGT GAGGTGGGCGGATCACTTGAGGTCAGGAGTTCCAGAGCAGCCTGGCCAACATGGTGAAACCCTGT T G ZNF841,ZNF432 Ensembl:ENSG00000197608,Ensembl:ENSG00000256087 Protein coding,Protein coding 3'UTR,intron GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line - 24183664,31158229 RNA-Seq:(High) rs1568532975 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196065,RMVar_hsa_circ_120820,RMVar_hsa_circ_106922,RMVar_hsa_circ_356345,RMVar_hsa_circ_196064,RMVar_hsa_circ_341674 15177 RMVar_ID_15177 Human_SNP_ID_669081864 A-to-I Human chr19 - 52064907 52064907 52064907 GATAGTTCTCATGAGGTCTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGCGG GATAGTTCTCATGAGGTCTGGCTCATGCCTGTTATCCCAGCACTTTGGGAGGCTGAGGTGGGCGG T A ZNF841,ZNF432 Ensembl:ENSG00000197608,Ensembl:ENSG00000256087 Protein coding,Protein coding 3'UTR,intron GSE38233;GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs535923398 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196065,RMVar_hsa_circ_120820,RMVar_hsa_circ_106922,RMVar_hsa_circ_356345,RMVar_hsa_circ_196064,RMVar_hsa_circ_341674 15178 RMVar_ID_15178 Human_SNP_ID_669083875 A-to-I Human chr19 - 52072707 52072707 52072707 TCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCATCTGCCACCATGCTTG TCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTGGCTGGGATTACAGGCATCTGCCACCATGCTTG T C ZNF841,ZNF432 Ensembl:ENSG00000197608,Ensembl:ENSG00000256087 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs963264383 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196065,RMVar_hsa_circ_120820,RMVar_hsa_circ_106922,RMVar_hsa_circ_196067,RMVar_hsa_circ_356345,RMVar_hsa_circ_196064,RMVar_hsa_circ_196068 15179 RMVar_ID_15179 Human_SNP_ID_669100905 A-to-I Human chr19 - 52143062 52143062 52143062 ACGTGTGCGTCTTATTGCGACGCTTTCCAAACAATGACGTTCCCTTCGTCATCTGGCTTCTGCGG ACGTGTGCGTCTTATTGCGACGCTTTCCAAACGATGACGTTCCCTTCGTCATCTGGCTTCTGCGG T C AC011468.2 Ensembl:ENSG00000267827 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878948549 Functional Loss SNV dbSNP153 33..33 33 - - - 15180 RMVar_ID_15180 Human_SNP_ID_669100914 A-to-I Human chr19 - 52143099 52143099 52143099 TGAAGGTGGTAGGCCTTAGAGCCACGGCGGCAACACAACGTGTGCGTCTTATTGCGACGCTTTCC TGAAGGTGGTAGGCCTTAGAGCCACGGCGGCAGCACAACGTGTGCGTCTTATTGCGACGCTTTCC T C AC011468.2 Ensembl:ENSG00000267827 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879071830 Functional Loss SNV dbSNP153 33..33 33 - - - 15181 RMVar_ID_15181 Human_SNP_ID_669100915 A-to-I Human chr19 - 52143100 52143100 52143100 CTGAAGGTGGTAGGCCTTAGAGCCACGGCGGCAACACAACGTGTGCGTCTTATTGCGACGCTTTC CTGAAGGTGGTAGGCCTTAGAGCCACGGCGGCGACACAACGTGTGCGTCTTATTGCGACGCTTTC T C AC011468.2 Ensembl:ENSG00000267827 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879000598 Functional Loss SNV dbSNP153 33..33 33 - - - 15182 RMVar_ID_15182 Human_SNP_ID_669113708 A-to-I Human chr19 + 52191040 52191040 52191040 AGCCACCACGCCCGACTAATTTTTGTATTTTTAGCAGAGACGGGGTTTCACCATGTTGGCCAGGC AGCCACCACGCCCGACTAATTTTTGTATTTTTCGCAGAGACGGGGTTTCACCATGTTGGCCAGGC A C PPP2R1A Ensembl:ENSG00000105568 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs544619665 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123181,RMVar_hsa_circ_196083,RMVar_hsa_circ_88534,RMVar_hsa_circ_196082 15183 RMVar_ID_15183 Human_SNP_ID_669113709 A-to-I Human chr19 + 52191040 52191040 52191040 AGCCACCACGCCCGACTAATTTTTGTATTTTTAGCAGAGACGGGGTTTCACCATGTTGGCCAGGC AGCCACCACGCCCGACTAATTTTTGTATTTTTGGCAGAGACGGGGTTTCACCATGTTGGCCAGGC A G PPP2R1A Ensembl:ENSG00000105568 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs544619665 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123181,RMVar_hsa_circ_196083,RMVar_hsa_circ_88534,RMVar_hsa_circ_196082 15184 RMVar_ID_15184 Human_SNP_ID_669114511 A-to-I Human chr19 + 52194033 52194033 52194033 TGCTCAGGAGACTGAGGTCGGAGGATTGCTTGAACCAGGGAGATCGAGGCTGCGGTGAGAGCCTG TGCTCAGGAGACTGAGGTCGGAGGATTGCTTGGACCAGGGAGATCGAGGCTGCGGTGAGAGCCTG A G PPP2R1A Ensembl:ENSG00000105568 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277770121 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123181,RMVar_hsa_circ_196083,RMVar_hsa_circ_88534,RMVar_hsa_circ_196082 15185 RMVar_ID_15185 Human_SNP_ID_669122567 A-to-I Human chr19 + 52225197 52225197 52225197 GCACCACCACGCCCTGCTAATTTTGTGTTTTTAGTAGGGACAGGGTTTCTCCATGTTGGTTTGGC GCACCACCACGCCCTGCTAATTTTGTGTTTTTGGTAGGGACAGGGTTTCTCCATGTTGGTTTGGC A G PPP2R1A Ensembl:ENSG00000105568 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs999209653 Functional Loss SNV dbSNP153 33..33 33 - - - 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_196108 15186 RMVar_ID_15186 Human_SNP_ID_669135908 A-to-I Human chr19 + 52279612 52279612 52279612 AAAGCAATGGGTTAGTGCAGTAGTATAAGCCTATAATTTGAGCTTCTTGGGAGGCTGAGATGGTA AAAGCAATGGGTTAGTGCAGTAGTATAAGCCTGTAATTTGAGCTTCTTGGGAGGCTGAGATGGTA A G ZNF766 Ensembl:ENSG00000196214 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs955678692 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115022,RMVar_hsa_circ_196112 15187 RMVar_ID_15187 Human_SNP_ID_669136948 A-to-I Human chr19 + 52283283 52283283 52283283 CACAGCACATCTTGATTCTTTCTTTTATAAACAGGAATCTGTCTTCCTGACCTGAGTATTATCTC CACAGCACATCTTGATTCTTTCTTTTATAAACGGGAATCTGTCTTCCTGACCTGAGTATTATCTC A G ZNF766 Ensembl:ENSG00000196214 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1229584060 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115022,RMVar_hsa_circ_196113,RMVar_hsa_circ_196112,RMVar_hsa_circ_275657 15188 RMVar_ID_15188 Human_SNP_ID_669137116 A-to-I Human chr19 + 52283807 52283807 52283807 GTCTCCAGGCTGGAGTGCAATGGCGTGATCTCAGCTCACTGCAACCTCCGCCTCCCGGGTACAAG GTCTCCAGGCTGGAGTGCAATGGCGTGATCTCCGCTCACTGCAACCTCCGCCTCCCGGGTACAAG A C ZNF766 Ensembl:ENSG00000196214 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs955550300 Functional Loss SNV dbSNP153 33..33 33 - - - 15189 RMVar_ID_15189 Human_SNP_ID_669139400 A-to-I Human chr19 + 52290998 52290998 52290998 TCACTCAAGTTTCACATCTTGCACGACATCAGAAAATTCACACTGGAGAGAAACCTTACAAATGT TCACTCAAGTTTCACATCTTGCACGACATCAGGAAATTCACACTGGAGAGAAACCTTACAAATGT A G ZNF766 Ensembl:ENSG00000196214 Protein coding CDS GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1423256915 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_505646,Human_miRNA_ID_512854 15190 RMVar_ID_15190 Human_SNP_ID_669139607 A-to-I Human chr19 + 52291691 52291691 52291691 TGAGGCAGGAGAATTGCTTGAATCCAGGAGGCAGAGGTTGTTGCAGTGAGCTGAGATCGCGCCAC TGAGGCAGGAGAATTGCTTGAATCCAGGAGGCGGAGGTTGTTGCAGTGAGCTGAGATCGCGCCAC A G ZNF766 Ensembl:ENSG00000196214 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1407484127 Functional Loss SNV dbSNP153 33..33 33 - - - 15191 RMVar_ID_15191 Human_SNP_ID_669141733 A-to-I Human chr19 + 52298613 52298612 52298614 AGATTGCGCCATTGCACTCCAGGCTGGGCGACAAGAGCAAAACTCCGTCTCAGGGAAAAAAAAAA AGATTGCGCCATTGCACTCCAGGCTGGGCGAC__GAGCAAAACTCCGTCTCAGGGAAAAAAAAAA CAA C ZNF480 Ensembl:ENSG00000198464 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256748951 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_93839,RMVar_hsa_circ_196116 15192 RMVar_ID_15192 Human_SNP_ID_669141734 A-to-I Human chr19 + 52298613 52298612 52298613 AGATTGCGCCATTGCACTCCAGGCTGGGCGACAAGAGCAAAACTCCGTCTCAGGGAAAAAAAAAA AGATTGCGCCATTGCACTCCAGGCTGGGCGAC_AGAGCAAAACTCCGTCTCAGGGAAAAAAAAAA CA C ZNF480 Ensembl:ENSG00000198464 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1488056544 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_93839,RMVar_hsa_circ_196116 15193 RMVar_ID_15193 Human_SNP_ID_669142031 A-to-I Human chr19 + 52299793 52299793 52299793 TCAGCTCACTGCAACATCCATCTCCCAGTTTCAAGCATTTCTCCTGCCTCAGCCTCCCAAGTAGC TCAGCTCACTGCAACATCCATCTCCCAGTTTCCAGCATTTCTCCTGCCTCAGCCTCCCAAGTAGC A C ZNF480 Ensembl:ENSG00000198464 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs192398940 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93839,RMVar_hsa_circ_196116 15194 RMVar_ID_15194 Human_SNP_ID_669170789 A-to-I Human chr19 + 52407125 52407125 52407125 CGCCACGATGCCTGGCTAATTTTTGGTATTTTATGTGGAGATGGGGTTTCACCATGTTACACAGG CGCCACGATGCCTGGCTAATTTTTGGTATTTTGTGTGGAGATGGGGTTTCACCATGTTACACAGG A G ZNF528 Ensembl:ENSG00000167555 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs750597033 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196128,RMVar_hsa_circ_127966,RMVar_hsa_circ_196147,RMVar_hsa_circ_119006,RMVar_hsa_circ_196148,RMVar_hsa_circ_75721,RMVar_hsa_circ_196150 15195 RMVar_ID_15195 Human_SNP_ID_669170790 A-to-I Human chr19 + 52407125 52407125 52407125 CGCCACGATGCCTGGCTAATTTTTGGTATTTTATGTGGAGATGGGGTTTCACCATGTTACACAGG CGCCACGATGCCTGGCTAATTTTTGGTATTTTTTGTGGAGATGGGGTTTCACCATGTTACACAGG A T ZNF528 Ensembl:ENSG00000167555 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs750597033 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196128,RMVar_hsa_circ_127966,RMVar_hsa_circ_196147,RMVar_hsa_circ_119006,RMVar_hsa_circ_196148,RMVar_hsa_circ_75721,RMVar_hsa_circ_196150 15196 RMVar_ID_15196 Human_SNP_ID_669211617 A-to-I Human chr19 + 52544254 52544254 52544254 AATTCAGAGTTTACAGCAGCCTCAAACTCCTGAGCTCAACTAATCGCTACTGTAGCCTCCCAAAG AATTCAGAGTTTACAGCAGCCTCAAACTCCTGGGCTCAACTAATCGCTACTGTAGCCTCCCAAAG A G ZNF808 Ensembl:ENSG00000198482 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs372725649 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116818,RMVar_hsa_circ_196156,RMVar_hsa_circ_107441,RMVar_hsa_circ_196155,RMVar_hsa_circ_39058 15197 RMVar_ID_15197 Human_SNP_ID_669213605 A-to-I Human chr19 + 52551267 52551267 52551267 CCAGCTTCTTGTGAGGCTGAGACAGGAGAGTCACTTGAACCTGGGAGGTGGATGGTGCAGTGAAC CCAGCTTCTTGTGAGGCTGAGACAGGAGAGTCCCTTGAACCTGGGAGGTGGATGGTGCAGTGAAC A C ZNF808 Ensembl:ENSG00000198482 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs370247216 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116818,RMVar_hsa_circ_196155,RMVar_hsa_circ_39058 15198 RMVar_ID_15198 Human_SNP_ID_669213755 A-to-I Human chr19 + 52551793 52551793 52551793 GGGAGGTCAAGGGGGGTGGATTACTTAAGGTCAGGAGTTTGAGACCAGCCTGGCCAACATGGTGA GGGAGGTCAAGGGGGGTGGATTACTTAAGGTCGGGAGTTTGAGACCAGCCTGGCCAACATGGTGA A G ZNF808 Ensembl:ENSG00000198482 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1259149641 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116818,RMVar_hsa_circ_196155,RMVar_hsa_circ_39058 15199 RMVar_ID_15199 Human_SNP_ID_669215401 A-to-I Human chr19 + 52556375 52556375 52556375 TGAGATGGAGTGTCACTCTTGTTGCCCAGCCTAGAGTGCAATGATGTGATCTCAGCTCACCACAA TGAGATGGAGTGTCACTCTTGTTGCCCAGCCTGGAGTGCAATGATGTGATCTCAGCTCACCACAA A G ZNF808,ZNF701 Ensembl:ENSG00000198482,Ensembl:ENSG00000167562 Protein coding,Protein coding intron,3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1412522818 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_685344,Human_miRNA_ID_887892,Human_miRNA_ID_1064536,Human_miRNA_ID_1075846,Human_miRNA_ID_2275742,Human_miRNA_ID_2401636,Human_miRNA_ID_2495562,Human_miRNA_ID_2501484,Human_miRNA_ID_3109512,Human_miRNA_ID_3110960 RMVar_hsa_circ_116818,RMVar_hsa_circ_196155 15200 RMVar_ID_15200 Human_SNP_ID_669215425 A-to-I Human chr19 + 52556466 52556466 52556466 CCTCTGCCTCAGCCTCCCTAGTTGCTGGGATTACAGGCATGTGCCACCACACCCGGCTAATTTTT CCTCTGCCTCAGCCTCCCTAGTTGCTGGGATTGCAGGCATGTGCCACCACACCCGGCTAATTTTT A G ZNF808,ZNF701 Ensembl:ENSG00000198482,Ensembl:ENSG00000167562 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1387986287 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_138423 RMVar_hsa_circ_116818,RMVar_hsa_circ_196155 15201 RMVar_ID_15201 Human_SNP_ID_669215675 A-to-I Human chr19 + 52557341 52557341 52557341 CAGGCTGGAGTGCAATGGTGCGATCTGGTGTCACTGCAACGTCTGCCTCCCGGGTTCAAGGCATT CAGGCTGGAGTGCAATGGTGCGATCTGGTGTCGCTGCAACGTCTGCCTCCCGGGTTCAAGGCATT A G ZNF808,ZNF701 Ensembl:ENSG00000198482,Ensembl:ENSG00000167562 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1414019703 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116818,RMVar_hsa_circ_196155 15202 RMVar_ID_15202 Human_SNP_ID_669216094 A-to-I Human chr19 + 52558511 52558511 52558511 CTTGTGCCTCAGCCTCCCGAGTAGCTGGGACTATAGGCGTGTGCCACCACGCCCAGCTAATTTTT CTTGTGCCTCAGCCTCCCGAGTAGCTGGGACTGTAGGCGTGTGCCACCACGCCCAGCTAATTTTT A G ZNF808,ZNF701 Ensembl:ENSG00000198482,Ensembl:ENSG00000167562 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027554731 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116818,RMVar_hsa_circ_196155 15203 RMVar_ID_15203 Human_SNP_ID_669217173 A-to-I Human chr19 + 52561603 52561603 52561603 GAGTTTCGTTCTTGTTTCCCAGGCTGGAGTGCAATGGCGCAATCTCGGCTCACCGCAACCTCTGC GAGTTTCGTTCTTGTTTCCCAGGCTGGAGTGCGATGGCGCAATCTCGGCTCACCGCAACCTCTGC A G ZNF808,ZNF701 Ensembl:ENSG00000198482,Ensembl:ENSG00000167562 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs933964274 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116818,RMVar_hsa_circ_196155 15204 RMVar_ID_15204 Human_SNP_ID_669217205 A-to-I Human chr19 + 52561687 52561687 52561687 CTCCTGCCTGAGGCTCCCAAGTAGCTGGGATTACAGGCGTGTACCACCACACCCAGCTAATTTTG CTCCTGCCTGAGGCTCCCAAGTAGCTGGGATTTCAGGCGTGTACCACCACACCCAGCTAATTTTG A T ZNF808,ZNF701 Ensembl:ENSG00000198482,Ensembl:ENSG00000167562 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs111896799 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116818,RMVar_hsa_circ_196155 15205 RMVar_ID_15205 Human_SNP_ID_669217251 A-to-I Human chr19 + 52561758 52561757 52561758 TATTAGAGATGGTGTTTTTCCATGTTAGTCAGACTGCTCTCAAGCTCCCGACCTCAGGAGATCCA TATTAGAGATGGTGTTTTTCCATGTTAGTCAG_CTGCTCTCAAGCTCCCGACCTCAGGAGATCCA GA G ZNF808,ZNF701 Ensembl:ENSG00000198482,Ensembl:ENSG00000167562 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878991883 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_116818,RMVar_hsa_circ_196155 15206 RMVar_ID_15206 Human_SNP_ID_669217253 A-to-I Human chr19 + 52561758 52561758 52561758 TATTAGAGATGGTGTTTTTCCATGTTAGTCAGACTGCTCTCAAGCTCCCGACCTCAGGAGATCCA TATTAGAGATGGTGTTTTTCCATGTTAGTCAGCCTGCTCTCAAGCTCCCGACCTCAGGAGATCCA A C ZNF808,ZNF701 Ensembl:ENSG00000198482,Ensembl:ENSG00000167562 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879214136 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116818,RMVar_hsa_circ_196155 15207 RMVar_ID_15207 Human_SNP_ID_669217254 A-to-I Human chr19 + 52561758 52561758 52561758 TATTAGAGATGGTGTTTTTCCATGTTAGTCAGACTGCTCTCAAGCTCCCGACCTCAGGAGATCCA TATTAGAGATGGTGTTTTTCCATGTTAGTCAGGCTGCTCTCAAGCTCCCGACCTCAGGAGATCCA A G ZNF808,ZNF701 Ensembl:ENSG00000198482,Ensembl:ENSG00000167562 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879214136 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116818,RMVar_hsa_circ_196155 15208 RMVar_ID_15208 Human_SNP_ID_669217256 A-to-I Human chr19 + 52561767 52561767 52561767 TGGTGTTTTTCCATGTTAGTCAGACTGCTCTCAAGCTCCCGACCTCAGGAGATCCACCCGCCTCG TGGTGTTTTTCCATGTTAGTCAGACTGCTCTCGAGCTCCCGACCTCAGGAGATCCACCCGCCTCG A G ZNF808,ZNF701 Ensembl:ENSG00000198482,Ensembl:ENSG00000167562 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878946804 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116818,RMVar_hsa_circ_196155 15209 RMVar_ID_15209 Human_SNP_ID_669217262 A-to-I Human chr19 + 52561790 52561790 52561790 ACTGCTCTCAAGCTCCCGACCTCAGGAGATCCACCCGCCTCGGTCTCCCAAAGTGCTGGAATTAC ACTGCTCTCAAGCTCCCGACCTCAGGAGATCCGCCCGCCTCGGTCTCCCAAAGTGCTGGAATTAC A G ZNF808,ZNF701 Ensembl:ENSG00000198482,Ensembl:ENSG00000167562 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1399316285 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116818,RMVar_hsa_circ_196155 15210 RMVar_ID_15210 Human_SNP_ID_669217502 A-to-I Human chr19 + 52562829 52562829 52562829 AGAGTCTTGCCCTGTTACCCAGGCTGGAGTGCAATGGCATGATCTCGGCTCACTGCAACCTACGC AGAGTCTTGCCCTGTTACCCAGGCTGGAGTGCCATGGCATGATCTCGGCTCACTGCAACCTACGC A C ZNF808,ZNF701 Ensembl:ENSG00000198482,Ensembl:ENSG00000167562 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1235927268 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2275744,Human_miRNA_ID_2401638,Human_miRNA_ID_2495564,Human_miRNA_ID_2501486,Human_miRNA_ID_3109514,Human_miRNA_ID_3110962 RMVar_hsa_circ_116818,RMVar_hsa_circ_196155 15211 RMVar_ID_15211 Human_SNP_ID_669218398 A-to-I Human chr19 + 52566259 52566259 52566259 GCGATCTCGGATCACTGAAACCTCTGCCTCCCAGGTACTACGGATTCTCCTGTCTCAGCACCCCA GCGATCTCGGATCACTGAAACCTCTGCCTCCCGGGTACTACGGATTCTCCTGTCTCAGCACCCCA A G ZNF701 Ensembl:ENSG00000167562 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1258366110 Functional Loss SNV dbSNP153 33..33 33 - - - 15212 RMVar_ID_15212 Human_SNP_ID_669218835 A-to-I Human chr19 + 52567580 52567580 52567580 GAGTTTCACTCTAGTTCCCTGGGCTGGAGTACAATGTCATGATCATGGCTCACCACAGCTTCCAT GAGTTTCACTCTAGTTCCCTGGGCTGGAGTACGATGTCATGATCATGGCTCACCACAGCTTCCAT A G ZNF701 Ensembl:ENSG00000167562 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs932097472 Functional Loss SNV dbSNP153 33..33 33 - - - 15213 RMVar_ID_15213 Human_SNP_ID_669218840 A-to-I Human chr19 + 52567604 52567604 52567604 TGGAGTACAATGTCATGATCATGGCTCACCACAGCTTCCATTTTCTGGGCTCAAGCGATTCTCCT TGGAGTACAATGTCATGATCATGGCTCACCACGGCTTCCATTTTCTGGGCTCAAGCGATTCTCCT A G ZNF701 Ensembl:ENSG00000167562 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs779519461 Functional Loss SNV dbSNP153 33..33 33 - - - 15214 RMVar_ID_15214 Human_SNP_ID_669218863 A-to-I Human chr19 + 52567697 52567697 52567697 CAGGCTCATGCCACCACTCCAGGCTAATTTTTATATTTGTAGTAGAGACGGGGTTTCTCTATATT CAGGCTCATGCCACCACTCCAGGCTAATTTTTGTATTTGTAGTAGAGACGGGGTTTCTCTATATT A G ZNF701 Ensembl:ENSG00000167562 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1281097784 Functional Loss SNV dbSNP153 33..33 33 - - - 15215 RMVar_ID_15215 Human_SNP_ID_669218870 A-to-I Human chr19 + 52567727 52567727 52567727 TTATATTTGTAGTAGAGACGGGGTTTCTCTATATTGGTCAGGCTGGTCTCGAACTCCCGACCTCA TTATATTTGTAGTAGAGACGGGGTTTCTCTATGTTGGTCAGGCTGGTCTCGAACTCCCGACCTCA A G ZNF701 Ensembl:ENSG00000167562 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs533506210 Functional Loss SNV dbSNP153 33..33 33 - - - 15216 RMVar_ID_15216 Human_SNP_ID_669218890 A-to-I Human chr19 + 52567785 52567785 52567785 GACCTCAGGCCATCCGCCGTCCTCAGCCTACCAAAGGGCTGGGATTACAGGCTTGAGCCACCGCG GACCTCAGGCCATCCGCCGTCCTCAGCCTACCTAAGGGCTGGGATTACAGGCTTGAGCCACCGCG A T ZNF701 Ensembl:ENSG00000167562 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1470092995 Functional Loss SNV dbSNP153 33..33 33 - - - 15217 RMVar_ID_15217 Human_SNP_ID_669218991 A-to-I Human chr19 + 52568185 52568185 52568185 CCTGACGTCAGGAATTAGAAACCAGCCTGGCCAACATGGGGAAACCCCGTCTCTACTGAAAATAC CCTGACGTCAGGAATTAGAAACCAGCCTGGCCGACATGGGGAAACCCCGTCTCTACTGAAAATAC A G ZNF701 Ensembl:ENSG00000167562 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1309097311 Functional Loss SNV dbSNP153 33..33 33 - - - 15218 RMVar_ID_15218 Human_SNP_ID_669218994 A-to-I Human chr19 + 52568188 52568188 52568188 GACGTCAGGAATTAGAAACCAGCCTGGCCAACATGGGGAAACCCCGTCTCTACTGAAAATACAAA GACGTCAGGAATTAGAAACCAGCCTGGCCAACGTGGGGAAACCCCGTCTCTACTGAAAATACAAA A G ZNF701 Ensembl:ENSG00000167562 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs928844743 Functional Loss SNV dbSNP153 33..33 33 - - - 15219 RMVar_ID_15219 Human_SNP_ID_669219014 A-to-I Human chr19 + 52568253 52568253 52568253 GCCATTAGCCGGGCATGGTGGCGCACGCCTGTATTTTCAGCTATTTGGGAGGCTGAGGCAGGAGA GCCATTAGCCGGGCATGGTGGCGCACGCCTGTGTTTTCAGCTATTTGGGAGGCTGAGGCAGGAGA A G ZNF701 Ensembl:ENSG00000167562 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1366742657 Functional Loss SNV dbSNP153 33..33 33 - - - 15220 RMVar_ID_15220 Human_SNP_ID_669221945 A-to-I Human chr19 + 52577179 52577179 52577179 TACAGTGCAGTGATACGATCTTGGCTAACAGCAGCCTCCACCTCCCAGGCTCAAAGGATTTTTGT TACAGTGCAGTGATACGATCTTGGCTAACAGCGGCCTCCACCTCCCAGGCTCAAAGGATTTTTGT A G ZNF701 Ensembl:ENSG00000167562 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs905628744 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196161 15221 RMVar_ID_15221 Human_SNP_ID_669228594 A-to-I Human chr19 + 52598647 52598647 52598647 AAATAAACTCAGGGCCCGGAGCGGTGGCTCACACCTGTAATCCCAGCACTTTGAGAGGCCAAGGA AAATAAACTCAGGGCCCGGAGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGAGAGGCCAAGGA A G lnc-ZNF701-1,lnc-ZNF701-1:2 RNACentral:URS00008B80E1,RNACentral:URS0000D5C466 lincRNA,lincRNA intron,exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1020921849 Functional Loss SNV dbSNP153 33..33 33 - - - 15222 RMVar_ID_15222 Human_SNP_ID_669234418 A-to-I Human chr19 - 52617468 52617468 52617468 CCTGGGCCTCCCAAAGTGTTGGGATTACAGGCATGAGCCACTGCTCCCGGCCTACTGTCACTTCT CCTGGGCCTCCCAAAGTGTTGGGATTACAGGCGTGAGCCACTGCTCCCGGCCTACTGTCACTTCT T C ZNF83 Ensembl:ENSG00000167766 Protein coding intron GSE47997;GSE107867 K562 cells&HepG2 cells;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 23474544,30559470 RNA-Seq:(High) rs997415261 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96700,RMVar_hsa_circ_196164,RMVar_hsa_circ_196163,RMVar_hsa_circ_196165,RMVar_hsa_circ_349281 15223 RMVar_ID_15223 Human_SNP_ID_669234420 A-to-I Human chr19 - 52617474 52617474 52617474 CACCTGCCTGGGCCTCCCAAAGTGTTGGGATTACAGGCATGAGCCACTGCTCCCGGCCTACTGTC CACCTGCCTGGGCCTCCCAAAGTGTTGGGATTGCAGGCATGAGCCACTGCTCCCGGCCTACTGTC T C ZNF83 Ensembl:ENSG00000167766 Protein coding intron GSE47997;GSE38233;GSE100210;GSE107867 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 23474544,24183664,29129909,30559470 RNA-Seq:(High) rs772805808 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96700,RMVar_hsa_circ_196164,RMVar_hsa_circ_196163,RMVar_hsa_circ_196165,RMVar_hsa_circ_349281 15224 RMVar_ID_15224 Human_SNP_ID_669234424 A-to-I Human chr19 - 52617486 52617485 52617486 CTTCAGGTGATCCACCTGCCTGGGCCTCCCAAAGTGTTGGGATTACAGGCATGAGCCACTGCTCC CTTCAGGTGATCCACCTGCCTGGGCCTCCCAA_GTGTTGGGATTACAGGCATGAGCCACTGCTCC CT C ZNF83 Ensembl:ENSG00000167766 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs201383529 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_96700,RMVar_hsa_circ_196164,RMVar_hsa_circ_196163,RMVar_hsa_circ_196165,RMVar_hsa_circ_349281 15225 RMVar_ID_15225 Human_SNP_ID_669234425 A-to-I Human chr19 - 52617487 52617487 52617487 ACTTCAGGTGATCCACCTGCCTGGGCCTCCCAAAGTGTTGGGATTACAGGCATGAGCCACTGCTC ACTTCAGGTGATCCACCTGCCTGGGCCTCCCAGAGTGTTGGGATTACAGGCATGAGCCACTGCTC T C ZNF83 Ensembl:ENSG00000167766 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1195283616 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96700,RMVar_hsa_circ_196164,RMVar_hsa_circ_196163,RMVar_hsa_circ_196165,RMVar_hsa_circ_349281 15226 RMVar_ID_15226 Human_SNP_ID_669234436 A-to-I Human chr19 - 52617548 52617548 52617548 TTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGTGTTTGAACTCCTGACTT TTTTGTATTTTTAGTAGAGACAGGGTTTCACCGTGTTGGCCAGGCTGTGTTTGAACTCCTGACTT T C ZNF83 Ensembl:ENSG00000167766 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs961322937 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96700,RMVar_hsa_circ_196164,RMVar_hsa_circ_196163,RMVar_hsa_circ_196165,RMVar_hsa_circ_349281 15227 RMVar_ID_15227 Human_SNP_ID_669234437 A-to-I Human chr19 - 52617551 52617551 52617551 AATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGTGTTTGAACTCCTGA AATTTTTGTATTTTTAGTAGAGACAGGGTTTCCCCATGTTGGCCAGGCTGTGTTTGAACTCCTGA T G ZNF83 Ensembl:ENSG00000167766 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs956324831 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96700,RMVar_hsa_circ_196164,RMVar_hsa_circ_196163,RMVar_hsa_circ_196165,RMVar_hsa_circ_349281 15228 RMVar_ID_15228 Human_SNP_ID_669234439 A-to-I Human chr19 - 52617559 52617559 52617559 GCCCAGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGTGTTTGA GCCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGTGTTTGA T C ZNF83 Ensembl:ENSG00000167766 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs372468720 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96700,RMVar_hsa_circ_196164,RMVar_hsa_circ_196163,RMVar_hsa_circ_196165,RMVar_hsa_circ_349281 15229 RMVar_ID_15229 Human_SNP_ID_669234442 A-to-I Human chr19 - 52617568 52617568 52617568 TGCCACCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGC TGCCACCATGCCCAGCTAATTTTTGTATTTTTGGTAGAGACAGGGTTTCACCATGTTGGCCAGGC T C ZNF83 Ensembl:ENSG00000167766 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1297666248 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96700,RMVar_hsa_circ_196164,RMVar_hsa_circ_196163,RMVar_hsa_circ_196165,RMVar_hsa_circ_349281 15230 RMVar_ID_15230 Human_SNP_ID_669234445 A-to-I Human chr19 - 52617587 52617587 52617587 AGCTGGGACTGCAGTCACATGCCACCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGACAGGGT AGCTGGGACTGCAGTCACATGCCACCATGCCCGGCTAATTTTTGTATTTTTAGTAGAGACAGGGT T C ZNF83 Ensembl:ENSG00000167766 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1397145781 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96700,RMVar_hsa_circ_196164,RMVar_hsa_circ_196163,RMVar_hsa_circ_196165,RMVar_hsa_circ_349281 15231 RMVar_ID_15231 Human_SNP_ID_669234447 A-to-I Human chr19 - 52617593 52617593 52617593 CCAAGTAGCTGGGACTGCAGTCACATGCCACCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGA CCAAGTAGCTGGGACTGCAGTCACATGCCACCGTGCCCAGCTAATTTTTGTATTTTTAGTAGAGA T C ZNF83 Ensembl:ENSG00000167766 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1171963852 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96700,RMVar_hsa_circ_196164,RMVar_hsa_circ_196163,RMVar_hsa_circ_196165,RMVar_hsa_circ_349281 15232 RMVar_ID_15232 Human_SNP_ID_669234463 A-to-I Human chr19 - 52617644 52617644 52617644 TCACTGTAACCTCCACCTCTGGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGA TCACTGTAACCTCCACCTCTGGGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGA T C ZNF83 Ensembl:ENSG00000167766 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs773818644 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_138498 RMVar_hsa_circ_96700,RMVar_hsa_circ_196164,RMVar_hsa_circ_196163,RMVar_hsa_circ_196165,RMVar_hsa_circ_349281 15233 RMVar_ID_15233 Human_SNP_ID_669234464 A-to-I Human chr19 - 52617649 52617649 52617649 TCGGTTCACTGTAACCTCCACCTCTGGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGC TCGGTTCACTGTAACCTCCACCTCTGGGGTTCCAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGC T G ZNF83 Ensembl:ENSG00000167766 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1325218971 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96700,RMVar_hsa_circ_196164,RMVar_hsa_circ_196163,RMVar_hsa_circ_196165,RMVar_hsa_circ_349281 15234 RMVar_ID_15234 Human_SNP_ID_669234494 A-to-I Human chr19 - 52617725 52617725 52617725 ATTTTTTTTTTTTTTTTTTTTTTTTTTTTGAGACAATCTCACTCTGTTGCCCAGGCTGGAGTGCA ATTTTTTTTTTTTTTTTTTTTTTTTTTTTGAGGCAATCTCACTCTGTTGCCCAGGCTGGAGTGCA T C ZNF83 Ensembl:ENSG00000167766 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1291583396 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96700,RMVar_hsa_circ_196164,RMVar_hsa_circ_196163,RMVar_hsa_circ_196165,RMVar_hsa_circ_349281 15235 RMVar_ID_15235 Human_SNP_ID_669234637 A-to-I Human chr19 - 52618168 52618168 52618168 ATTATCACCTGAACCTGGGAGGCAATGGTTGCAGTGAGCCGAGAATGCATGACTGCACTCCAGCC ATTATCACCTGAACCTGGGAGGCAATGGTTGCGGTGAGCCGAGAATGCATGACTGCACTCCAGCC T C ZNF83 Ensembl:ENSG00000167766 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1446426382 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96700,RMVar_hsa_circ_196164,RMVar_hsa_circ_196163,RMVar_hsa_circ_196165,RMVar_hsa_circ_349281 15236 RMVar_ID_15236 Human_SNP_ID_669234641 A-to-I Human chr19 - 52618189 52618189 52618189 TACTAGAAAGGCTAAGGTAAGATTATCACCTGAACCTGGGAGGCAATGGTTGCAGTGAGCCGAGA TACTAGAAAGGCTAAGGTAAGATTATCACCTGTACCTGGGAGGCAATGGTTGCAGTGAGCCGAGA T A ZNF83 Ensembl:ENSG00000167766 Protein coding intron GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line - 24183664,31158229 RNA-Seq:(High) rs1295758560 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96700,RMVar_hsa_circ_196164,RMVar_hsa_circ_196163,RMVar_hsa_circ_196165,RMVar_hsa_circ_349281 15237 RMVar_ID_15237 Human_SNP_ID_669234646 A-to-I Human chr19 - 52618217 52618217 52618217 CGTGATGGCACATGTCTGTAATCCCAGGTACTAGAAAGGCTAAGGTAAGATTATCACCTGAACCT CGTGATGGCACATGTCTGTAATCCCAGGTACTGGAAAGGCTAAGGTAAGATTATCACCTGAACCT T C ZNF83 Ensembl:ENSG00000167766 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1194681174 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96700,RMVar_hsa_circ_196164,RMVar_hsa_circ_196163,RMVar_hsa_circ_196165,RMVar_hsa_circ_349281 15238 RMVar_ID_15238 Human_SNP_ID_669234727 A-to-I Human chr19 - 52618443 52618443 52618443 CCTGGTGAACACAGTGAAACCCTGTCTCTACTAAAAATACAAAAAAAAATTAGCCGGGTGTGGTG CCTGGTGAACACAGTGAAACCCTGTCTCTACTGAAAATACAAAAAAAAATTAGCCGGGTGTGGTG T C ZNF83 Ensembl:ENSG00000167766 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs879703369 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96700,RMVar_hsa_circ_196164,RMVar_hsa_circ_196163,RMVar_hsa_circ_196165,RMVar_hsa_circ_349281 15239 RMVar_ID_15239 Human_SNP_ID_669234732 A-to-I Human chr19 - 52618463 52618463 52618463 GGTCAGGAGATCGAGACCATCCTGGTGAACACAGTGAAACCCTGTCTCTACTAAAAATACAAAAA GGTCAGGAGATCGAGACCATCCTGGTGAACACGGTGAAACCCTGTCTCTACTAAAAATACAAAAA T C ZNF83 Ensembl:ENSG00000167766 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs954081137 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96700,RMVar_hsa_circ_196164,RMVar_hsa_circ_196163,RMVar_hsa_circ_196165,RMVar_hsa_circ_349281 15240 RMVar_ID_15240 Human_SNP_ID_669234805 A-to-I Human chr19 - 52618670 52618670 52618670 ATGGCTGGCAAGGCGTGGTGACTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAAGCTTGTGG ATGGCTGGCAAGGCGTGGTGACTCATGCCTGTTATCCCAGCACTTTGGGAGGCCAAAGCTTGTGG T A ZNF83 Ensembl:ENSG00000167766 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs527518537 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2039890,Human_Splice_Rec_2039891,Human_Splice_Rec_2039954 RMVar_hsa_circ_96700,RMVar_hsa_circ_196164,RMVar_hsa_circ_196163,RMVar_hsa_circ_196165,RMVar_hsa_circ_349281 15241 RMVar_ID_15241 Human_SNP_ID_669234806 A-to-I Human chr19 - 52618670 52618670 52618670 ATGGCTGGCAAGGCGTGGTGACTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAAGCTTGTGG ATGGCTGGCAAGGCGTGGTGACTCATGCCTGTCATCCCAGCACTTTGGGAGGCCAAAGCTTGTGG T G ZNF83 Ensembl:ENSG00000167766 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs527518537 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2039890,Human_Splice_Rec_2039891,Human_Splice_Rec_2039954 RMVar_hsa_circ_96700,RMVar_hsa_circ_196164,RMVar_hsa_circ_196163,RMVar_hsa_circ_196165,RMVar_hsa_circ_349281 15242 RMVar_ID_15242 Human_SNP_ID_669234811 A-to-I Human chr19 - 52618682 52618682 52618682 GCTTAAAACCTTATGGCTGGCAAGGCGTGGTGACTCATGCCTGTAATCCCAGCACTTTGGGAGGC GCTTAAAACCTTATGGCTGGCAAGGCGTGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGC T C ZNF83 Ensembl:ENSG00000167766 Protein coding intron GSE47997;GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line - 23474544,24183664,31158229 RNA-Seq:(High) rs570297098 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2039890,Human_Splice_Rec_2039891,Human_Splice_Rec_2039954 RMVar_hsa_circ_96700,RMVar_hsa_circ_196164,RMVar_hsa_circ_196163,RMVar_hsa_circ_196165,RMVar_hsa_circ_349281 15243 RMVar_ID_15243 Human_SNP_ID_669240220 A-to-I Human chr19 - 52636228 52636228 52636228 TAACTGCAGCCTGGTCCTCCTGGGCTCAAGTAATCCTCCTACGTCAGCTTCCTAAGTAGCTGGGA TAACTGCAGCCTGGTCCTCCTGGGCTCAAGTAGTCCTCCTACGTCAGCTTCCTAAGTAGCTGGGA T C ZNF83 Ensembl:ENSG00000167766 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs906324469 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96700,RMVar_hsa_circ_196163,RMVar_hsa_circ_42184 15244 RMVar_ID_15244 Human_SNP_ID_669240355 A-to-I Human chr19 - 52636765 52636765 52636765 TGTAATCCCAGCTACTCTGAAGGCCGAGGCAGAAGGATCACTTGAACCCAGGAGGTCCAGGCTGC TGTAATCCCAGCTACTCTGAAGGCCGAGGCAGGAGGATCACTTGAACCCAGGAGGTCCAGGCTGC T C ZNF83 Ensembl:ENSG00000167766 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs866255287 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96700,RMVar_hsa_circ_196163,RMVar_hsa_circ_42184 15245 RMVar_ID_15245 Human_SNP_ID_669240366 A-to-I Human chr19 - 52636793 52636793 52636793 AAAACAACCGGGCATGATAGTGTGCACCTGTAATCCCAGCTACTCTGAAGGCCGAGGCAGAAGGA AAAACAACCGGGCATGATAGTGTGCACCTGTACTCCCAGCTACTCTGAAGGCCGAGGCAGAAGGA T G ZNF83 Ensembl:ENSG00000167766 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs571885417 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96700,RMVar_hsa_circ_196163,RMVar_hsa_circ_42184 15246 RMVar_ID_15246 Human_SNP_ID_669242020 A-to-I Human chr19 - 52642392 52642392 52642392 TGGTGGTGCCTGCCTATAATCCCAGCTACTCAAGAGGCTGAGGCAGGAGAATCGCTTGAACCCAA TGGTGGTGCCTGCCTATAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACCCAA T C ZNF83 Ensembl:ENSG00000167766 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs201187697 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96700,RMVar_hsa_circ_196163,RMVar_hsa_circ_42184 15247 RMVar_ID_15247 Human_SNP_ID_669242022 A-to-I Human chr19 - 52642401 52642401 52642401 AGCCAGGCGTGGTGGTGCCTGCCTATAATCCCAGCTACTCAAGAGGCTGAGGCAGGAGAATCGCT AGCCAGGCGTGGTGGTGCCTGCCTATAATCCCGGCTACTCAAGAGGCTGAGGCAGGAGAATCGCT T C ZNF83 Ensembl:ENSG00000167766 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1026574017 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96700,RMVar_hsa_circ_196163,RMVar_hsa_circ_42184 15248 RMVar_ID_15248 Human_SNP_ID_669242023 A-to-I Human chr19 - 52642406 52642406 52642406 AAATTAGCCAGGCGTGGTGGTGCCTGCCTATAATCCCAGCTACTCAAGAGGCTGAGGCAGGAGAA AAATTAGCCAGGCGTGGTGGTGCCTGCCTATAGTCCCAGCTACTCAAGAGGCTGAGGCAGGAGAA T C ZNF83 Ensembl:ENSG00000167766 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs911556022 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96700,RMVar_hsa_circ_196163,RMVar_hsa_circ_42184 15249 RMVar_ID_15249 Human_SNP_ID_669242024 A-to-I Human chr19 - 52642409 52642409 52642409 ACAAAATTAGCCAGGCGTGGTGGTGCCTGCCTATAATCCCAGCTACTCAAGAGGCTGAGGCAGGA ACAAAATTAGCCAGGCGTGGTGGTGCCTGCCTGTAATCCCAGCTACTCAAGAGGCTGAGGCAGGA T C ZNF83 Ensembl:ENSG00000167766 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs556683735 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96700,RMVar_hsa_circ_196163,RMVar_hsa_circ_42184 15250 RMVar_ID_15250 Human_SNP_ID_669242032 A-to-I Human chr19 - 52642450 52642450 52642450 CAGCCTGACCGACATGGAGATACCCGGTCTTTACTAAAAATACAAAATTAGCCAGGCGTGGTGGT CAGCCTGACCGACATGGAGATACCCGGTCTTTGCTAAAAATACAAAATTAGCCAGGCGTGGTGGT T C ZNF83 Ensembl:ENSG00000167766 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1439806123 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96700,RMVar_hsa_circ_196163,RMVar_hsa_circ_42184 15251 RMVar_ID_15251 Human_SNP_ID_669242636 A-to-I Human chr19 - 52644950 52644950 52644950 ACTGGAGTGCAATGGTGAGATCTCAGCTCACCACAACCTCCTCCTCCCGGGTTCAAGCTATTCTC ACTGGAGTGCAATGGTGAGATCTCAGCTCACCGCAACCTCCTCCTCCCGGGTTCAAGCTATTCTC T C ZNF83 Ensembl:ENSG00000167766 Protein coding intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1457596640 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96700,RMVar_hsa_circ_196163,RMVar_hsa_circ_42184 15252 RMVar_ID_15252 Human_SNP_ID_669242938 A-to-I Human chr19 - 52646063 52646063 52646063 TGGTGGCATGCACCTGTAGTCACAGCTACTCAAGATGCTGAGGCACGAGAATCACTTGAACCTGG TGGTGGCATGCACCTGTAGTCACAGCTACTCAGGATGCTGAGGCACGAGAATCACTTGAACCTGG T C ZNF83 Ensembl:ENSG00000167766 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs79944020 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96700,RMVar_hsa_circ_196163,RMVar_hsa_circ_42184 15253 RMVar_ID_15253 Human_SNP_ID_669242990 A-to-I Human chr19 - 52646300 52646300 52646300 ATGCAAAGGATCTTCCTGCCTTGGACCCTCAAAGTACCAGCATTACAGGGATTAGCCATCACACC ATGCAAAGGATCTTCCTGCCTTGGACCCTCAAGGTACCAGCATTACAGGGATTAGCCATCACACC T C ZNF83 Ensembl:ENSG00000167766 Protein coding intron GSE99789;GSE126723:GSM3611833,GSM3611834,GSM3611835 esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BERP35T4 cell line - 29796672,31158229 RNA-Seq:(High) rs1568561086 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96700,RMVar_hsa_circ_196163,RMVar_hsa_circ_42184 15254 RMVar_ID_15254 Human_SNP_ID_669243047 A-to-I Human chr19 - 52646543 52646543 52646543 TTTAATTAACTAATTAATTAATATTTTCAGATAGCATCTGGCTCTATCACCCAGGATGGAGTGCC TTTAATTAACTAATTAATTAATATTTTCAGATCGCATCTGGCTCTATCACCCAGGATGGAGTGCC T G ZNF83 Ensembl:ENSG00000167766 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1485516107 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_138500 RMVar_hsa_circ_96700,RMVar_hsa_circ_196163,RMVar_hsa_circ_42184 15255 RMVar_ID_15255 Human_SNP_ID_669244065 A-to-I Human chr19 - 52650445 52650445 52650445 CGAGACCAGCCTGACCCACATGGAGAAACCCCATCTTTACTAAAAATACAAAATTAGCCAGACTT CGAGACCAGCCTGACCCACATGGAGAAACCCCGTCTTTACTAAAAATACAAAATTAGCCAGACTT T C AC022150.4,ZNF83 Ensembl:ENSG00000269825,Ensembl:ENSG00000167766 lincRNA,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1282314671 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96700,RMVar_hsa_circ_196163,RMVar_hsa_circ_42184 15256 RMVar_ID_15256 Human_SNP_ID_669244388 A-to-I Human chr19 - 52651848 52651848 52651848 TCAAGAAGAATGGGCAGGGTGCAGTTGCTCACACCTATAATCCCAGCACTTTGGGAGGCCAAGGC TCAAGAAGAATGGGCAGGGTGCAGTTGCTCACTCCTATAATCCCAGCACTTTGGGAGGCCAAGGC T A AC022150.4,ZNF83 Ensembl:ENSG00000269825,Ensembl:ENSG00000167766 lincRNA,Protein coding exon,intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs776245710 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3589767 RMVar_hsa_circ_96700,RMVar_hsa_circ_196163,RMVar_hsa_circ_42184 15257 RMVar_ID_15257 Human_SNP_ID_669244389 A-to-I Human chr19 - 52651848 52651848 52651848 TCAAGAAGAATGGGCAGGGTGCAGTTGCTCACACCTATAATCCCAGCACTTTGGGAGGCCAAGGC TCAAGAAGAATGGGCAGGGTGCAGTTGCTCACGCCTATAATCCCAGCACTTTGGGAGGCCAAGGC T C AC022150.4,ZNF83 Ensembl:ENSG00000269825,Ensembl:ENSG00000167766 lincRNA,Protein coding exon,intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs776245710 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3589767 RMVar_hsa_circ_96700,RMVar_hsa_circ_196163,RMVar_hsa_circ_42184 15258 RMVar_ID_15258 Human_SNP_ID_669244457 A-to-I Human chr19 - 52652176 52652176 52652176 CCTCGGCCTCCCAAAGTGCTGGTATTACAGGCATGAGCCACCACGCCCAGTGTGGCAATGTCTTT CCTCGGCCTCCCAAAGTGCTGGTATTACAGGCGTGAGCCACCACGCCCAGTGTGGCAATGTCTTT T C AC022150.4,ZNF83 Ensembl:ENSG00000269825,Ensembl:ENSG00000167766 lincRNA,Protein coding exon,intron GSE100210;GSE107867 HepG2 cell line;ASD brains,cerebellum - 29129909,30559470 RNA-Seq:(High) rs1286532758 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96700,RMVar_hsa_circ_196163,RMVar_hsa_circ_42184 15259 RMVar_ID_15259 Human_SNP_ID_669244486 A-to-I Human chr19 - 52652273 52652273 52652273 CTCCACCAAGCCTGGCTAATTTTTATGTTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCTGGT CTCCACCAAGCCTGGCTAATTTTTATGTTTTTGGTAGAGACAGGGTTTCACCATGTTGGCCTGGT T C AC022150.4,ZNF83 Ensembl:ENSG00000269825,Ensembl:ENSG00000167766 lincRNA,Protein coding exon,intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1191555608 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96700,RMVar_hsa_circ_196163,RMVar_hsa_circ_42184 15260 RMVar_ID_15260 Human_SNP_ID_669244490 A-to-I Human chr19 - 52652311 52652311 52652311 CCTTCCTAGCCTCCTGAGTAGCTGGGACTACAAGCATGCTCCACCAAGCCTGGCTAATTTTTATG CCTTCCTAGCCTCCTGAGTAGCTGGGACTACAGGCATGCTCCACCAAGCCTGGCTAATTTTTATG T C AC022150.4,ZNF83 Ensembl:ENSG00000269825,Ensembl:ENSG00000167766 lincRNA,Protein coding exon,intron GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs994151042 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5099410 RMVar_hsa_circ_96700,RMVar_hsa_circ_196163,RMVar_hsa_circ_42184 15261 RMVar_ID_15261 Human_SNP_ID_669258827 A-to-I Human chr19 - 52702108 52702108 52702108 GTCAGTAGAGACAGGCTCTCACTGTGTTGGCCAGGCTGGTCTCAAACTACTGACTTCTGGTGATC GTCAGTAGAGACAGGCTCTCACTGTGTTGGCCCGGCTGGTCTCAAACTACTGACTTCTGGTGATC T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1399000446 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_526334 15262 RMVar_ID_15262 Human_SNP_ID_669258831 A-to-I Human chr19 - 52702128 52702128 52702128 CCTGGCTAGGTTTTTGCATTGTCAGTAGAGACAGGCTCTCACTGTGTTGGCCAGGCTGGTCTCAA CCTGGCTAGGTTTTTGCATTGTCAGTAGAGACGGGCTCTCACTGTGTTGGCCAGGCTGGTCTCAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs868074720 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_526334,Human_RBP_ID_13504869,Human_RBP_ID_17930484 15263 RMVar_ID_15263 Human_SNP_ID_669258975 A-to-I Human chr19 - 52702582 52702582 52702582 CTCTGTCGCCTTGGATGGAGGGCAGTGGTGCAATCTCAGCTCACTGCAACCTCTGCCTCCTGGGA CTCTGTCGCCTTGGATGGAGGGCAGTGGTGCAGTCTCAGCTCACTGCAACCTCTGCCTCCTGGGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1221913226 Functional Loss SNV dbSNP153 33..33 33 - - - 15264 RMVar_ID_15264 Human_SNP_ID_669259183 A-to-I Human chr19 - 52703367 52703367 52703367 TGGGGCATGAGAATTGCTTAAACCTAGGAGGTAGAAGTTGCAGTGAACCAAAATTGTGCCACTAT TGGGGCATGAGAATTGCTTAAACCTAGGAGGTGGAAGTTGCAGTGAACCAAAATTGTGCCACTAT T C ZNF611 Ensembl:ENSG00000213020 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1442935627 Functional Loss SNV dbSNP153 33..33 33 - - - 15265 RMVar_ID_15265 Human_SNP_ID_669259201 A-to-I Human chr19 - 52703410 52703409 52703410 GGGGGTGTTGGTGTGCACCTTTAGTTCCAGCTACTTGGGAGGCTGGGGCATGAGAATTGCTTAAA GGGGGTGTTGGTGTGCACCTTTAGTTCCAGCT_CTTGGGAGGCTGGGGCATGAGAATTGCTTAAA GT G ZNF611 Ensembl:ENSG00000213020 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1397749950 Functional Loss DEL dbSNP153 33..33 33 - - - 15266 RMVar_ID_15266 Human_SNP_ID_669259202 A-to-I Human chr19 - 52703410 52703410 52703410 GGGGGTGTTGGTGTGCACCTTTAGTTCCAGCTACTTGGGAGGCTGGGGCATGAGAATTGCTTAAA GGGGGTGTTGGTGTGCACCTTTAGTTCCAGCTGCTTGGGAGGCTGGGGCATGAGAATTGCTTAAA T C ZNF611 Ensembl:ENSG00000213020 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs541970183 Functional Loss SNV dbSNP153 33..33 33 - - - 15267 RMVar_ID_15267 Human_SNP_ID_669259316 A-to-I Human chr19 - 52703652 52703652 52703652 GTGAGGCGGAGCTTGCAGGGAGTCGAGATCGCACCACTGGGCTCCAGCCTGGGCGACAGAGTGAG GTGAGGCGGAGCTTGCAGGGAGTCGAGATCGCGCCACTGGGCTCCAGCCTGGGCGACAGAGTGAG T C ZNF611 Ensembl:ENSG00000213020 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs974574486 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17930488 15268 RMVar_ID_15268 Human_SNP_ID_669259353 A-to-I Human chr19 - 52703766 52703766 52703766 TAACAGGGTGAATCCCTGTCTCTACTAAAAATACAAAAAATTAGCTGGGCATGGTGGCTGGCGCC TAACAGGGTGAATCCCTGTCTCTACTAAAAATGCAAAAAATTAGCTGGGCATGGTGGCTGGCGCC T C ZNF611 Ensembl:ENSG00000213020 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1210164448 Functional Loss SNV dbSNP153 33..33 33 - - - 15269 RMVar_ID_15269 Human_SNP_ID_669259373 A-to-I Human chr19 - 52703858 52703858 52703858 GGCCAGGCACGGAGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCCGAGGCAGGCAGATCACG GGCCAGGCACGGAGGCTCATGCCTATAATCCCGGCACTTTGGGAGGCCGAGGCAGGCAGATCACG T C ZNF611 Ensembl:ENSG00000213020 Protein coding 3'UTR GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1249719637 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1358272 15270 RMVar_ID_15270 Human_SNP_ID_669260879 A-to-I Human chr19 - 52708422 52708422 52708422 GCGATCTGGGCTCACTGCAGTCTCCATCTTCCAGGTTCATGCCATTCTCCTGCCTCAGCTTCCAG GCGATCTGGGCTCACTGCAGTCTCCATCTTCCGGGTTCATGCCATTCTCCTGCCTCAGCTTCCAG T C ZNF611 Ensembl:ENSG00000213020 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947220704 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2040107 15271 RMVar_ID_15271 Human_SNP_ID_669289911 A-to-I Human chr19 - 52804527 52804527 52804527 GTCTCTACTAAAAATGCAAAAATTAGCTGTGTATGGTGGCGTGCGCCTGTAATCCCAGCTACTTG GTCTCTACTAAAAATGCAAAAATTAGCTGTGTGTGGTGGCGTGCGCCTGTAATCCCAGCTACTTG T C ZNF28 Ensembl:ENSG00000198538 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs538186761 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128048,RMVar_hsa_circ_196171 15272 RMVar_ID_15272 Human_SNP_ID_669290167 A-to-I Human chr19 - 52805464 52805464 52805464 CACCACTACACCCAGCTAAGTTTTGTATTTTTAGTAGAGATGGGGTTCCACCATGTTGGTTGGCC CACCACTACACCCAGCTAAGTTTTGTATTTTTGGTAGAGATGGGGTTCCACCATGTTGGTTGGCC T C ZNF28 Ensembl:ENSG00000198538 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs914832806 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128048,RMVar_hsa_circ_196171,RMVar_hsa_circ_117051,RMVar_hsa_circ_196174 15273 RMVar_ID_15273 Human_SNP_ID_669290171 A-to-I Human chr19 - 52805487 52805487 52805487 GAGTAGCTGCAACTACAAGTGTGCACCACTACACCCAGCTAAGTTTTGTATTTTTAGTAGAGATG GAGTAGCTGCAACTACAAGTGTGCACCACTACCCCCAGCTAAGTTTTGTATTTTTAGTAGAGATG T G ZNF28 Ensembl:ENSG00000198538 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs923350515 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128048,RMVar_hsa_circ_196171,RMVar_hsa_circ_117051,RMVar_hsa_circ_196174 15274 RMVar_ID_15274 Human_SNP_ID_669291803 A-to-I Human chr19 - 52810650 52810650 52810650 CTCTAGCCCGGCCCCTGTAGACGCGACCCCAGAGCCTGCTGTTAAAACCACTGTAGAATGGAGAG CTCTAGCCCGGCCCCTGTAGACGCGACCCCAGGGCCTGCTGTTAAAACCACTGTAGAATGGAGAG T C ZNF28 Ensembl:ENSG00000198538 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879080730 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60331 15275 RMVar_ID_15275 Human_SNP_ID_669291805 A-to-I Human chr19 - 52810652 52810652 52810652 CGCTCTAGCCCGGCCCCTGTAGACGCGACCCCAGAGCCTGCTGTTAAAACCACTGTAGAATGGAG CGCTCTAGCCCGGCCCCTGTAGACGCGACCCCGGAGCCTGCTGTTAAAACCACTGTAGAATGGAG T C ZNF28 Ensembl:ENSG00000198538 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878955808 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60331 15276 RMVar_ID_15276 Human_SNP_ID_669300692 A-to-I Human chr19 - 52839344 52839340 52839344 TAATTCCAGCACTTTGAGAGGCAAAGACAGGTAGGTCACTGGAGCTCACGAGTTTGAGAACAGCC TAATTCCAGCACTTTGAGAGGCAAAGACAGGT____CACTGGAGCTCACGAGTTTGAGAACAGCC GACCT G ZNF468,ZNF28 Ensembl:ENSG00000204604,Ensembl:ENSG00000198538 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1474492640 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_6782321 Human_miRNA_ID_468521,Human_miRNA_ID_606676,Human_miRNA_ID_2154679,Human_miRNA_ID_2226533 RMVar_hsa_circ_81347,RMVar_hsa_circ_196175 15277 RMVar_ID_15277 Human_SNP_ID_669305312 A-to-I Human chr19 - 52854334 52854334 52854334 CAACATATTTTTAACATTCAGGATTGACTTCTAAAGACTGTTGGTACGTGAGAAAGAAACCCAGA CAACATATTTTTAACATTCAGGATTGACTTCTGAAGACTGTTGGTACGTGAGAAAGAAACCCAGA T C ZNF468,ZNF28 Ensembl:ENSG00000204604,Ensembl:ENSG00000198538 Protein coding,Protein coding 5'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904683492 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2040214,Human_Splice_Rec_2040215,Human_Splice_Rec_2040220,Human_Splice_Rec_2040221,Human_Splice_Rec_2040228,Human_Splice_Rec_2040229,Human_Splice_Rec_2040242,Human_Splice_Rec_2040243,Human_Splice_Rec_2040250,Human_Splice_Rec_2040251 RMVar_hsa_circ_10988,RMVar_hsa_circ_3121 15278 RMVar_ID_15278 Human_SNP_ID_669312467 A-to-I Human chr19 - 52878528 52878528 52878528 AAGTGATGCACAGGACAGGTGTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGC AAGTGATGCACAGGACAGGTGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGC T C ZNF320 Ensembl:ENSG00000182986 Protein coding intron GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs1008098141 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196177,RMVar_hsa_circ_196178,RMVar_hsa_circ_100352,RMVar_hsa_circ_356978 15279 RMVar_ID_15279 Human_SNP_ID_669312853 A-to-I Human chr19 - 52880159 52880157 52880159 TATTTTTAGTAGAGACTGGGTTTCACCGTGTTAGCTAGGATGGTCTCGATCTTCTGTCCTTAAAA TATTTTTAGTAGAGACTGGGTTTCACCGTGTT__CTAGGATGGTCTCGATCTTCTGTCCTTAAAA GCT G ZNF320 Ensembl:ENSG00000182986 Protein coding intron GSE38233;GSE99789 cultured B-cells;esophageal squamous carcinoma cells,EC109 - 24183664,29796672 RNA-Seq:(High) rs1568709901 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_27471019 RMVar_hsa_circ_196177,RMVar_hsa_circ_196178,RMVar_hsa_circ_100352,RMVar_hsa_circ_356978 15280 RMVar_ID_15280 Human_SNP_ID_669314210 A-to-I Human chr19 - 52885171 52885171 52885171 TTGAGACACAGTCTCAGTCTCTCACCCAGGCTAAAGTGCAGTGGTGTGATCTTGGGTCACTGCAA TTGAGACACAGTCTCAGTCTCTCACCCAGGCTGAAGTGCAGTGGTGTGATCTTGGGTCACTGCAA T C ZNF320 Ensembl:ENSG00000182986 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1263469218 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196178,RMVar_hsa_circ_100352,RMVar_hsa_circ_356978 15281 RMVar_ID_15281 Human_SNP_ID_669317524 A-to-I Human chr19 - 52896491 52896491 52896491 TTGCTCAGGCTGGTCTCCAACTCCAGGGCTCAAGCGATCCAGCTGTATCGCCCTCCCAAAATGCT TTGCTCAGGCTGGTCTCCAACTCCAGGGCTCACGCGATCCAGCTGTATCGCCCTCCCAAAATGCT T G ZNF320 Ensembl:ENSG00000182986 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs761330704 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196178,RMVar_hsa_circ_100352 15282 RMVar_ID_15282 Human_SNP_ID_669323575 A-to-I Human chr19 - 52917655 52917655 52917657 CCAATGACATGAACATGAGAAGAGGTTGCAGTAGGCATGGTCCTGGGAAGGGCTCACACACAGAC CCAATGACATGAACATGAGAAGAGGTTGCACTGGGCATGGTCCTGGGAAGGGCTCACACACAGAC TAC CAG ZNF888 Ensembl:ENSG00000213793 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs386810607 Functional Loss MNV dbSNP153 31..33 33 - - - RMVar_hsa_circ_354970 15283 RMVar_ID_15283 Human_SNP_ID_669323576 A-to-I Human chr19 - 52917655 52917655 52917655 CCAATGACATGAACATGAGAAGAGGTTGCAGTAGGCATGGTCCTGGGAAGGGCTCACACACAGAC CCAATGACATGAACATGAGAAGAGGTTGCAGTGGGCATGGTCCTGGGAAGGGCTCACACACAGAC T C ZNF888 Ensembl:ENSG00000213793 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs539629428 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_354970 15284 RMVar_ID_15284 Human_SNP_ID_669326299 A-to-I Human chr19 - 52925410 52925410 52925410 GTCTCTACTAAAAATACAAAAATTAGCCCAGCATGGTAGCAGACGCCTGTAGTTCCAGCTATTCA GTCTCTACTAAAAATACAAAAATTAGCCCAGCGTGGTAGCAGACGCCTGTAGTTCCAGCTATTCA T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1338946965 Functional Loss SNV dbSNP153 33..33 33 - - - 15285 RMVar_ID_15285 Human_SNP_ID_669326528 A-to-I Human chr19 - 52926255 52926255 52926255 GGGTTCACCCCATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGTACTACAGACGCCCATGACCACA GGGTTCACCCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGTACTACAGACGCCCATGACCACA T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1421675107 Functional Loss SNV dbSNP153 33..33 33 - - - 15286 RMVar_ID_15286 Human_SNP_ID_669326539 A-to-I Human chr19 - 52926276 52926276 52926276 TCACTGCAAGCTCCGCCTCCTGGGTTCACCCCATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGTA TCACTGCAAGCTCCGCCTCCTGGGTTCACCCCGTTCTCCTGCCTCAGCCTCCCAAGTAGCTGGTA T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1247336591 Functional Loss SNV dbSNP153 33..33 33 - - - 15287 RMVar_ID_15287 Human_SNP_ID_669326647 A-to-I Human chr19 - 52926596 52926596 52926596 AGGCGTAGTGATGCATGCCTGTAATCTTAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCTTGAA AGGCGTAGTGATGCATGCCTGTAATCTTAGCTGCTCGGGAGGCTGAGGCAGGAGAATTGCTTGAA T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1057059430 Functional Loss SNV dbSNP153 33..33 33 - - - 15288 RMVar_ID_15288 Human_SNP_ID_669326732 A-to-I Human chr19 - 52926824 52926824 52926824 CCAGGAGGCGGAGGTTGCAGTGAGCCAAGATCACACCACTGCACTCCAACCTGGGTGACAGAGCG CCAGGAGGCGGAGGTTGCAGTGAGCCAAGATCGCACCACTGCACTCCAACCTGGGTGACAGAGCG T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1326008733 Functional Loss SNV dbSNP153 33..33 33 - - - 15289 RMVar_ID_15289 Human_SNP_ID_669326778 A-to-I Human chr19 - 52926918 52926918 52926918 TCTCTACTAAAAATACCAAAAATTAGCCAGGCATGGTGGTGTGCACCTGTAGTCCCAGCTACTCA TCTCTACTAAAAATACCAAAAATTAGCCAGGCGTGGTGGTGTGCACCTGTAGTCCCAGCTACTCA T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10404213 Functional Loss SNV dbSNP153 33..33 33 - - - 15290 RMVar_ID_15290 Human_SNP_ID_669326833 A-to-I Human chr19 - 52927035 52927035 52927035 AGTTTTGGCCAGGCAAAGAGGCTCACACCTGTAATCCCAGCATTTTGGGAGGCCAAGGCGGGAGC AGTTTTGGCCAGGCAAAGAGGCTCACACCTGTGATCCCAGCATTTTGGGAGGCCAAGGCGGGAGC T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1312910218 Functional Loss SNV dbSNP153 33..33 33 - - - 15291 RMVar_ID_15291 Human_SNP_ID_669326919 A-to-I Human chr19 - 52927245 52927245 52927245 GGGCATGGTGGGGCACGCCTGTATTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAACTGCTTGAT GGGCATGGTGGGGCACGCCTGTATTCCCAGCTCCTTGGGAGGCTGAGGCAGGAGAACTGCTTGAT T G ZNF321P Ensembl:ENSG00000213801 Pseudogene exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1262205297 Functional Loss SNV dbSNP153 33..33 33 - - - 15292 RMVar_ID_15292 Human_SNP_ID_669326963 A-to-I Human chr19 - 52927390 52927384 52927391 TTCCTGGCCAGGCGCAGTGGCTCAAGCCTGTAATCCCAGCATTTTGGGAGGCCGAGGTGGGCGGA TTCCTGGCCAGGCGCAGTGGCTCAAGCCTGT_______GCATTTTGGGAGGCCGAGGTGGGCGGA CTGGGATT C ZNF321P Ensembl:ENSG00000213801 Pseudogene exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1248143093 Functional Loss DEL dbSNP153 32..38 33 - - - 15293 RMVar_ID_15293 Human_SNP_ID_669326963 A-to-I Human chr19 - 52927391 52927384 52927391 TTTCCTGGCCAGGCGCAGTGGCTCAAGCCTGTAATCCCAGCATTTTGGGAGGCCGAGGTGGGCGG TTTCCTGGCCAGGCGCAGTGGCTCAAGCCTGT_______GCATTTTGGGAGGCCGAGGTGGGCGG CTGGGATT C ZNF321P Ensembl:ENSG00000213801 Pseudogene exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1248143093 Functional Loss DEL dbSNP153 33..39 33 - - - 15294 RMVar_ID_15294 Human_SNP_ID_669326970 A-to-I Human chr19 - 52927398 52927398 52927398 TTTGAGTTTTCCTGGCCAGGCGCAGTGGCTCAAGCCTGTAATCCCAGCATTTTGGGAGGCCGAGG TTTGAGTTTTCCTGGCCAGGCGCAGTGGCTCACGCCTGTAATCCCAGCATTTTGGGAGGCCGAGG T G ZNF321P Ensembl:ENSG00000213801 Pseudogene exon GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1210868393 Functional Loss SNV dbSNP153 33..33 33 - - - 15295 RMVar_ID_15295 Human_SNP_ID_669326978 A-to-I Human chr19 - 52927413 52927413 52927413 CGCAGGCGCAACTTTTTTGAGTTTTCCTGGCCAGGCGCAGTGGCTCAAGCCTGTAATCCCAGCAT CGCAGGCGCAACTTTTTTGAGTTTTCCTGGCCGGGCGCAGTGGCTCAAGCCTGTAATCCCAGCAT T C ZNF321P Ensembl:ENSG00000213801 Pseudogene exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs911351712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5261842 15296 RMVar_ID_15296 Human_SNP_ID_669327007 A-to-I Human chr19 - 52927492 52927492 52927492 TTGATCTCCTGACCTTGTGATCCACCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAA TTGATCTCCTGACCTTGTGATCCACCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAA T C ZNF321P Ensembl:ENSG00000213801 Pseudogene exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs976592579 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_139159 15297 RMVar_ID_15297 Human_SNP_ID_669327047 A-to-I Human chr19 - 52927639 52927639 52927639 TCACTGCAAGCTCCGCCTCCTGGGTTCACGTCATTTTCCTGTCTCAGCCTCCCCAGTAGCTGGGA TCACTGCAAGCTCCGCCTCCTGGGTTCACGTCTTTTTCCTGTCTCAGCCTCCCCAGTAGCTGGGA T A ZNF321P Ensembl:ENSG00000213801 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1052062277 Functional Loss SNV dbSNP153 33..33 33 - - - 15298 RMVar_ID_15298 Human_SNP_ID_669327061 A-to-I Human chr19 - 52927674 52927674 52927674 TCGCCCAAGCTGAAGTGCAGTGGTGCGATCTCAGCTCACTGCAAGCTCCGCCTCCTGGGTTCACG TCGCCCAAGCTGAAGTGCAGTGGTGCGATCTCGGCTCACTGCAAGCTCCGCCTCCTGGGTTCACG T C ZNF321P Ensembl:ENSG00000213801 Pseudogene exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs905099414 Functional Loss SNV dbSNP153 33..33 33 - - - 15299 RMVar_ID_15299 Human_SNP_ID_669327221 A-to-I Human chr19 - 52928243 52928243 52928243 AGTTTCACTCTTATTGCCCAGGCTGGAGTGCAATGGTGCAATCTTGGCTCACTGCACCCTCTGTC AGTTTCACTCTTATTGCCCAGGCTGGAGTGCAGTGGTGCAATCTTGGCTCACTGCACCCTCTGTC T C ZNF321P Ensembl:ENSG00000213801 Pseudogene exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs987722680 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9929782 15300 RMVar_ID_15300 Human_SNP_ID_669327939 A-to-I Human chr19 - 52930974 52930974 52930974 GAGTCTTGCTCTGCACCAGGCTGGAGTGCAGTAGTGCGATCTCGGCTCTCTGCAACCTCCACCTC GAGTCTTGCTCTGCACCAGGCTGGAGTGCAGTTGTGCGATCTCGGCTCTCTGCAACCTCCACCTC T A ZNF816-ZNF321P,ZNF321P Ensembl:ENSG00000221874,Ensembl:ENSG00000213801 Protein coding,Pseudogene intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1206132785 Functional Loss SNV dbSNP153 33..33 33 - - - 15301 RMVar_ID_15301 Human_SNP_ID_669330133 A-to-I Human chr19 - 52938373 52938373 52938373 TCTCTCCCTGCAACCTCTGTCTCCTGGGTTCAAGCGATTCTTGTGTCTCACCTCACAAGTAGCTG TCTCTCCCTGCAACCTCTGTCTCCTGGGTTCAGGCGATTCTTGTGTCTCACCTCACAAGTAGCTG T C ZNF816-ZNF321P,ZNF321P Ensembl:ENSG00000221874,Ensembl:ENSG00000213801 Protein coding,Pseudogene intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1351867086 Functional Loss SNV dbSNP153 33..33 33 - - - 15302 RMVar_ID_15302 Human_SNP_ID_669338076 A-to-I Human chr19 - 52966004 52966004 52966004 CAAAGCTACATAGAGGCTGGGTATGGTGGCTCAGGCCTCTAATCCCAGCACTTTGGGAGGCTGCG CAAAGCTACATAGAGGCTGGGTATGGTGGCTCCGGCCTCTAATCCCAGCACTTTGGGAGGCTGCG T G AC010328.3 Ensembl:ENSG00000269082 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1454787219 Functional Loss SNV dbSNP153 33..33 33 - - - 15303 RMVar_ID_15303 Human_SNP_ID_669342655 A-to-I Human chr19 - 52984202 52984202 52984202 GAGTCTCATTCTTTTGCCCAGGCTGGAGTGCAATGGCGCGATCTCGGCTCACTGCAACCTCCACC GAGTCTCATTCTTTTGCCCAGGCTGGAGTGCAGTGGCGCGATCTCGGCTCACTGCAACCTCCACC T C ZNF702P Ensembl:ENSG00000242779 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1016930605 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47073 15304 RMVar_ID_15304 Human_SNP_ID_669348238 A-to-I Human chr19 + 53004758 53004758 53004758 GTTGCTGATGCCTCAAAAAGTGTGCAGGTCTCAATTCTGAAGACAGAGTTCCTACCACTCCTGAG GTTGCTGATGCCTCAAAAAGTGTGCAGGTCTCGATTCTGAAGACAGAGTTCCTACCACTCCTGAG A G AC010328.2 Ensembl:ENSG00000268282 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879211707 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5586599 Human_miRNA_ID_1909167 15305 RMVar_ID_15305 Human_SNP_ID_669348252 A-to-I Human chr19 - 53004815 53004815 53004815 ATTGGGTAGCAGTCATGGCCAGCAGCCACGACACTGTTCTCTGAGACAAATGACACACTCAGGAG ATTGGGTAGCAGTCATGGCCAGCAGCCACGACGCTGTTCTCTGAGACAAATGACACACTCAGGAG T C ZNF702P Ensembl:ENSG00000242779 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878865762 Functional Loss SNV dbSNP153 33..33 33 - - - 15306 RMVar_ID_15306 Human_SNP_ID_669348437 A-to-I Human chr19 + 53005485 53005484 53005485 AATTGTCCACTAGAAAATTAAATAAAAGAACTAAATGTGGGAAAAAAAAAAAGAAAGAAAGAAAA AATTGTCCACTAGAAAATTAAATAAAAGAACT_AATGTGGGAAAAAAAAAAAGAAAGAAAGAAAA TA T - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs978547840 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_26475147 15307 RMVar_ID_15307 Human_SNP_ID_669366674 A-to-I Human chr19 - 53072258 53072258 53072258 GTCTTTACTAAAAATACAAAAATTAGCCAGGCATGATGGCACATGCCTGCAGTCCCAGCTATTCG GTCTTTACTAAAAATACAAAAATTAGCCAGGCGTGATGGCACATGCCTGCAGTCCCAGCTATTCG T C ZNF160 Ensembl:ENSG00000170949 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs329736 Functional Loss SNV dbSNP153 33..33 33 - - - 15308 RMVar_ID_15308 Human_SNP_ID_669366701 A-to-I Human chr19 - 53072375 53072375 53072375 AACTGTCAGGCCAGGTATAGAGGCTCACGCCTATAATCCCAGCACTTGGGGAGGCAGAGGCAGGC AACTGTCAGGCCAGGTATAGAGGCTCACGCCTGTAATCCCAGCACTTGGGGAGGCAGAGGCAGGC T C ZNF160 Ensembl:ENSG00000170949 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1272469480 Functional Loss SNV dbSNP153 33..33 33 - - - 15309 RMVar_ID_15309 Human_SNP_ID_669366778 A-to-I Human chr19 - 53072729 53072729 53072729 CTCCTGTCTCAGCCTCCCGAGTAGCTGGGATTACAGGCATGCGCCACCATGCCTGGTTAATTGTG CTCCTGTCTCAGCCTCCCGAGTAGCTGGGATTGCAGGCATGCGCCACCATGCCTGGTTAATTGTG T C ZNF160 Ensembl:ENSG00000170949 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs535924591 Functional Loss SNV dbSNP153 33..33 33 - - - 15310 RMVar_ID_15310 Human_SNP_ID_669366785 A-to-I Human chr19 - 53072766 53072766 53072766 GCTCACCGCAACTTCTGCCTCCTGGGTTCGAGAGATTCTCCTGTCTCAGCCTCCCGAGTAGCTGG GCTCACCGCAACTTCTGCCTCCTGGGTTCGAGCGATTCTCCTGTCTCAGCCTCCCGAGTAGCTGG T G ZNF160 Ensembl:ENSG00000170949 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1039422200 Functional Loss SNV dbSNP153 33..33 33 - - - 15311 RMVar_ID_15311 Human_SNP_ID_669367621 A-to-I Human chr19 - 53075788 53075788 53075788 GAATTCTGATGACCCCCTCCTTGAAATTGATTAGTTTGCTTGAGTGGCTCACATAACACAGGGAA GAATTCTGATGACCCCCTCCTTGAAATTGATTCGTTTGCTTGAGTGGCTCACATAACACAGGGAA T G ZNF160 Ensembl:ENSG00000170949 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs748642538 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33099,RMVar_hsa_circ_266993,RMVar_hsa_circ_370421,RMVar_hsa_circ_196189 15312 RMVar_ID_15312 Human_SNP_ID_669367657 A-to-I Human chr19 - 53075926 53075911 53075927 CATTCTGACACTGTCTATCTGGATATAGGGTCAGCTCCCATAGGCTGAGGGCTCAATCCCACAAC CATTCTGACACTGTCTATCTGGATATAGGGT________________AGGGCTCAATCCCACAAC TCAGCCTATGGGAGCTG T ZNF160 Ensembl:ENSG00000170949 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1456575438 Functional Loss DEL dbSNP153 32..47 33 - - - RMVar_hsa_circ_33099,RMVar_hsa_circ_266993,RMVar_hsa_circ_370421,RMVar_hsa_circ_196189 15313 RMVar_ID_15313 Human_SNP_ID_669404332 A-to-I Human chr19 + 53213955 53213955 53213955 AGAATTGCTTGAACCTGGGAGATGGAGGTTGCAGTGAGCTGAGATCATGCCACTGCACGCCAGCC AGAATTGCTTGAACCTGGGAGATGGAGGTTGCCGTGAGCTGAGATCATGCCACTGCACGCCAGCC A C AC092070.2 Ensembl:ENSG00000269001 Pseudogene exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1438105490 Functional Loss SNV dbSNP153 33..33 33 - - - 15314 RMVar_ID_15314 Human_SNP_ID_669404411 A-to-I Human chr19 + 53214208 53214208 53214208 CCTGGATTCCAGCAATTCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCGCGTGCCACCACA CCTGGATTCCAGCAATTCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCGTGCCACCACA A G AC092070.2 Ensembl:ENSG00000269001 Pseudogene exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs929000953 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17387910 15315 RMVar_ID_15315 Human_SNP_ID_669404412 A-to-I Human chr19 + 53214222 53214222 53214222 ATTCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCGCGTGCCACCACACCCGGTTAATTTTT ATTCTGCCTCAGCCTCCCAAGTAGCTGGGACTGCAGGCGCGTGCCACCACACCCGGTTAATTTTT A G AC092070.2 Ensembl:ENSG00000269001 Pseudogene exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1056755714 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17387910 15316 RMVar_ID_15316 Human_SNP_ID_669404674 A-to-I Human chr19 + 53215359 53215359 53215359 TGCCACCACCCCCAGCTAACTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTAGCCAGGA TGCCACCACCCCCAGCTAACTTTTGTATTTTTCGTAGAGACAGGGTTTCACCATGTTAGCCAGGA A C lnc-VN1R2-5,lnc-VN1R2-5:2,lnc-VN1R2-5:3,lnc-VN1R2-5:4,lnc-VN1R2-5:5,lnc-VN1R2-5:6 RNACentral:URS0000D5B8A3,RNACentral:URS0000D5BFE6,RNACentral:URS0000D5957B,RNACentral:URS00008BBA50,RNACentral:URS0000D5D65D,RNACentral:URS0000D5CFC0 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,intron,exon,exon,exon,exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs957143107 Functional Loss SNV dbSNP153 33..33 33 - - - 15317 RMVar_ID_15317 Human_SNP_ID_669410095 A-to-I Human chr19 - 53236141 53236141 53236141 GGAGTGCAGTGGCACCATCTCAGCTCACTGCAACCTCTGTCTCCCGGGTTCAAGCAATTCTCCTG GGAGTGCAGTGGCACCATCTCAGCTCACTGCATCCTCTGTCTCCCGGGTTCAAGCAATTCTCCTG T A ZNF677 Ensembl:ENSG00000197928 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs190638823 Functional Loss SNV dbSNP153 33..33 33 - - - 15318 RMVar_ID_15318 Human_SNP_ID_669443143 A-to-I Human chr19 + 53355374 53355374 53355374 CGTCCAAGCAATTCTGTCTCAGCCTCCTGAGTAGCTGGGACTACAGGCGCATGTCACCACACCTA CGTCCAAGCAATTCTGTCTCAGCCTCCTGAGTCGCTGGGACTACAGGCGCATGTCACCACACCTA A C ZNF845 Ensembl:ENSG00000213799 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1254105804 Functional Loss SNV dbSNP153 33..33 33 - - - 15319 RMVar_ID_15319 Human_SNP_ID_669443144 A-to-I Human chr19 + 53355374 53355374 53355374 CGTCCAAGCAATTCTGTCTCAGCCTCCTGAGTAGCTGGGACTACAGGCGCATGTCACCACACCTA CGTCCAAGCAATTCTGTCTCAGCCTCCTGAGTTGCTGGGACTACAGGCGCATGTCACCACACCTA A T ZNF845 Ensembl:ENSG00000213799 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1254105804 Functional Loss SNV dbSNP153 33..33 33 - - - 15320 RMVar_ID_15320 Human_SNP_ID_669443353 A-to-I Human chr19 + 53356260 53356260 53356260 ACAAGAAGAAACATCAAATTTACGATGAGACCAGACGCAGTGGCTCAGGCCTGTAATCCCAGCGG ACAAGAAGAAACATCAAATTTACGATGAGACCGGACGCAGTGGCTCAGGCCTGTAATCCCAGCGG A G ZNF845 Ensembl:ENSG00000213799 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs966416739 Functional Loss SNV dbSNP153 33..33 33 - - - 15321 RMVar_ID_15321 Human_SNP_ID_669449534 A-to-I Human chr19 + 53377295 53377295 53377295 CAACTCCTGGGTTCAAGCAATTCTCCTGCCTCAGTTTCCCGAGTAGCTGGGATTATAGGCATATG CAACTCCTGGGTTCAAGCAATTCTCCTGCCTCGGTTTCCCGAGTAGCTGGGATTATAGGCATATG A G ZNF525 Ensembl:ENSG00000203326 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs192643445 Functional Loss SNV dbSNP153 33..33 33 - - - 15322 RMVar_ID_15322 Human_SNP_ID_669449633 A-to-I Human chr19 + 53377648 53377648 53377648 ACAATCTTGGCTAACTGCAACCTCTGCCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGTTTCCCA ACAATCTTGGCTAACTGCAACCTCTGCCTCCCTGGTTCAAGCGATTCTCCTGCCTCAGTTTCCCA A T ZNF525 Ensembl:ENSG00000203326 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1341309982 Functional Loss SNV dbSNP153 33..33 33 - - - 15323 RMVar_ID_15323 Human_SNP_ID_669449644 A-to-I Human chr19 + 53377684 53377684 53377684 TCAAGCGATTCTCCTGCCTCAGTTTCCCAAGTAGCTGGGACTACAGGCATGTGCCACCACACCAG TCAAGCGATTCTCCTGCCTCAGTTTCCCAAGTGGCTGGGACTACAGGCATGTGCCACCACACCAG A G ZNF525 Ensembl:ENSG00000203326 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs935234078 Functional Loss SNV dbSNP153 33..33 33 - - - 15324 RMVar_ID_15324 Human_SNP_ID_669449645 A-to-I Human chr19 + 53377684 53377684 53377684 TCAAGCGATTCTCCTGCCTCAGTTTCCCAAGTAGCTGGGACTACAGGCATGTGCCACCACACCAG TCAAGCGATTCTCCTGCCTCAGTTTCCCAAGTTGCTGGGACTACAGGCATGTGCCACCACACCAG A T ZNF525 Ensembl:ENSG00000203326 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs935234078 Functional Loss SNV dbSNP153 33..33 33 - - - 15325 RMVar_ID_15325 Human_SNP_ID_669449756 A-to-I Human chr19 + 53378310 53378310 53378310 GAAACCCTGTCTCTACTAAAAATACAAGAATTAGCTGGGCGTGGTGGCACATGGCTGTTATCCCA GAAACCCTGTCTCTACTAAAAATACAAGAATTCGCTGGGCGTGGTGGCACATGGCTGTTATCCCA A C ZNF525 Ensembl:ENSG00000203326 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1310502940 Functional Loss SNV dbSNP153 33..33 33 - - - 15326 RMVar_ID_15326 Human_SNP_ID_669450039 A-to-I Human chr19 + 53379390 53379390 53379390 TTCCCACCTCGGCCTCCCAAAGTGCTGGAATTACAGGCATGAGCCACTGCACCCGGCTGTTAGTG TTCCCACCTCGGCCTCCCAAAGTGCTGGAATTGCAGGCATGAGCCACTGCACCCGGCTGTTAGTG A G ZNF525 Ensembl:ENSG00000203326 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs182074390 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2041041 15327 RMVar_ID_15327 Human_SNP_ID_669456683 A-to-I Human chr19 + 53402369 53402369 53402369 AGCTCCGCCTCCCGGGTTCACGCCATTCTCCTACTTCAGCCTCCCAAGTAGCTGGGACTACAGGC AGCTCCGCCTCCCGGGTTCACGCCATTCTCCTCCTTCAGCCTCCCAAGTAGCTGGGACTACAGGC A C ZNF765 Ensembl:ENSG00000196417 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1321729353 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_311675 15328 RMVar_ID_15328 Human_SNP_ID_669456709 A-to-I Human chr19 + 53402467 53402467 53402467 ATTTTTTACTAGAGACGGAGTTTCACCATGTTAGCCAGGATGGCCTTGAAATCCTGACCTCGTGA ATTTTTTACTAGAGACGGAGTTTCACCATGTTGGCCAGGATGGCCTTGAAATCCTGACCTCGTGA A G ZNF765 Ensembl:ENSG00000196417 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1248375381 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_311675 15329 RMVar_ID_15329 Human_SNP_ID_669456765 A-to-I Human chr19 + 53402615 53402615 53402615 AAAGTGTCTCTCTCTGTCAGCCCGGGTGGAGTACAATGGTGTGATCATGGCTCACTGCAATCTTG AAAGTGTCTCTCTCTGTCAGCCCGGGTGGAGTGCAATGGTGTGATCATGGCTCACTGCAATCTTG A G ZNF765 Ensembl:ENSG00000196417 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1032826172 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_311675 15330 RMVar_ID_15330 Human_SNP_ID_669457021 A-to-I Human chr19 + 53403588 53403588 53403588 ACAATTTTTGTGCCCCAGTGGCTCACGCCTGTAATCCCAGCACTTCGGGAGGCCGAGGCAGGCAA ACAATTTTTGTGCCCCAGTGGCTCACGCCTGTTATCCCAGCACTTCGGGAGGCCGAGGCAGGCAA A T ZNF765 Ensembl:ENSG00000196417 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1208092408 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_311675 15331 RMVar_ID_15331 Human_SNP_ID_669457465 A-to-I Human chr19 + 53405270 53405270 53405270 AGTACTTGAGAGGCCGAGGCAGGAGAATCACTAGAACCTGGGAGGTGGAGGTTGCAGTGAGCCAA AGTACTTGAGAGGCCGAGGCAGGAGAATCACTTGAACCTGGGAGGTGGAGGTTGCAGTGAGCCAA A T ZNF765 Ensembl:ENSG00000196417 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1298869255 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17568158 RMVar_hsa_circ_311675 15332 RMVar_ID_15332 Human_SNP_ID_669457787 A-to-I Human chr19 + 53406168 53406168 53406168 CTCCTGCCTCAGCCTTCCAAGTAGCTGAGATTACAGGCAGCCACCACCATGCCCAGCTAATTTTT CTCCTGCCTCAGCCTTCCAAGTAGCTGAGATTGCAGGCAGCCACCACCATGCCCAGCTAATTTTT A G ZNF765 Ensembl:ENSG00000196417 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1436018057 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_311675 15333 RMVar_ID_15333 Human_SNP_ID_669457905 A-to-I Human chr19 + 53406659 53406659 53406659 CAGTGCCACCGGATGCTGTGGCTCACGCCTGCAATCCCAGGACTTTGGGAGGCTGAGGTGGCTGG CAGTGCCACCGGATGCTGTGGCTCACGCCTGCCATCCCAGGACTTTGGGAGGCTGAGGTGGCTGG A C ZNF765 Ensembl:ENSG00000196417 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1432969270 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_311675 15334 RMVar_ID_15334 Human_SNP_ID_669457906 A-to-I Human chr19 + 53406659 53406659 53406659 CAGTGCCACCGGATGCTGTGGCTCACGCCTGCAATCCCAGGACTTTGGGAGGCTGAGGTGGCTGG CAGTGCCACCGGATGCTGTGGCTCACGCCTGCGATCCCAGGACTTTGGGAGGCTGAGGTGGCTGG A G ZNF765 Ensembl:ENSG00000196417 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1432969270 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_311675 15335 RMVar_ID_15335 Human_SNP_ID_669457932 A-to-I Human chr19 + 53406800 53406800 53406800 AGCCAAACGTGGTAGTGTGTGCGTGTAATCCCAGGTACTCAGGAGGCTGAGGCAGGAGAATGGCT AGCCAAACGTGGTAGTGTGTGCGTGTAATCCCGGGTACTCAGGAGGCTGAGGCAGGAGAATGGCT A G ZNF765 Ensembl:ENSG00000196417 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1047527384 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_311675 15336 RMVar_ID_15336 Human_SNP_ID_669457937 A-to-I Human chr19 + 53406841 53406841 53406841 GGAGGCTGAGGCAGGAGAATGGCTTGAACCCAAAAGGTGGAGGTTGCAGTGAGCTGAGATCGGGC GGAGGCTGAGGCAGGAGAATGGCTTGAACCCAGAAGGTGGAGGTTGCAGTGAGCTGAGATCGGGC A G ZNF765 Ensembl:ENSG00000196417 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs555055093 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_311675 15337 RMVar_ID_15337 Human_SNP_ID_669458146 A-to-I Human chr19 + 53407696 53407696 53407696 TAATTTGAAACCTTTTGGTGTGTATACTTTTTAGATATCTCTTCCAAATGCATGATGAAGGAGTT TAATTTGAAACCTTTTGGTGTGTATACTTTTTGGATATCTCTTCCAAATGCATGATGAAGGAGTT A G ZNF765 Ensembl:ENSG00000196417 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1397530971 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - RMVar_hsa_circ_311675 15338 RMVar_ID_15338 Human_SNP_ID_669459367 A-to-I Human chr19 + 53411553 53411553 53411553 GCCTCAGATGATCCACCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCGC GCCTCAGATGATCCACCCACCTCGGCCTCCCAGAGTGCTGGGATTACAGGCGTGAGCCACTGCGC A G ZNF765 Ensembl:ENSG00000196417 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1294971003 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_141076 RMVar_hsa_circ_311675 15339 RMVar_ID_15339 Human_SNP_ID_669467224 A-to-I Human chr19 + 53439150 53439150 53439150 AAAATTAGGCAGCCATGGTGGCAGGCGCCTGTAATCCCAGCTACCCAGGAGGCAAAGGCAGGAGA AAAATTAGGCAGCCATGGTGGCAGGCGCCTGTGATCCCAGCTACCCAGGAGGCAAAGGCAGGAGA A G TPM3P9,AC022137.3 Ensembl:ENSG00000241015,Ensembl:ENSG00000286261 Pseudogene,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1133126 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17131998 RMVar_hsa_circ_311675 15340 RMVar_ID_15340 Human_SNP_ID_669467244 A-to-I Human chr19 + 53439234 53439234 53439234 CAGAGGTTGCAGTGAGCTGAGATCGTGCCACTACACTCTAGCCTTGGTGACAGAACAAGACTCTG CAGAGGTTGCAGTGAGCTGAGATCGTGCCACTGCACTCTAGCCTTGGTGACAGAACAAGACTCTG A G TPM3P9,AC022137.3 Ensembl:ENSG00000241015,Ensembl:ENSG00000286261 Pseudogene,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1133128 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25447902 RMVar_hsa_circ_311675 15341 RMVar_ID_15341 Human_SNP_ID_669467607 A-to-I Human chr19 + 53440701 53440701 53440701 TAATTAAATTAATTAATAATTAGTATTTTGAGACAGGGCTGGCTCTATCGCCCAGGATGGAGTGC TAATTAAATTAATTAATAATTAGTATTTTGAGTCAGGGCTGGCTCTATCGCCCAGGATGGAGTGC A T TPM3P9,AC022137.3 Ensembl:ENSG00000241015,Ensembl:ENSG00000286261 Pseudogene,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs531392525 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17568159 RMVar_hsa_circ_311675 15342 RMVar_ID_15342 Human_SNP_ID_669467621 A-to-I Human chr19 + 53440715 53440715 53440715 AATAATTAGTATTTTGAGACAGGGCTGGCTCTATCGCCCAGGATGGAGTGCAGCATGATCTCTTC AATAATTAGTATTTTGAGACAGGGCTGGCTCTGTCGCCCAGGATGGAGTGCAGCATGATCTCTTC A G TPM3P9,AC022137.3 Ensembl:ENSG00000241015,Ensembl:ENSG00000286261 Pseudogene,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459066596 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17568159 RMVar_hsa_circ_311675 15343 RMVar_ID_15343 Human_SNP_ID_669467643 A-to-I Human chr19 + 53440788 53440788 53440788 GCCTCGACCTCCTGGGCTCAAACCATCCTCCTACCTCAGCTTCCTGAGTAGCTAAGGTCACAGGC GCCTCGACCTCCTGGGCTCAAACCATCCTCCTGCCTCAGCTTCCTGAGTAGCTAAGGTCACAGGC A G TPM3P9,AC022137.3 Ensembl:ENSG00000241015,Ensembl:ENSG00000286261 Pseudogene,Protein coding intron,intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1222568161 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17387755,Human_RBP_ID_17568160 RMVar_hsa_circ_311675 15344 RMVar_ID_15344 Human_SNP_ID_669467715 A-to-I Human chr19 + 53441080 53441080 53441080 GAGGCGAGTGGGTCACCTAAGGTGAGGAGTTCAAGAGCAGCCTGGCCAACATGGTGAAACCTGGT GAGGCGAGTGGGTCACCTAAGGTGAGGAGTTCTAGAGCAGCCTGGCCAACATGGTGAAACCTGGT A T TPM3P9,AC022137.3 Ensembl:ENSG00000241015,Ensembl:ENSG00000286261 Pseudogene,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1218773942 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25432524 RMVar_hsa_circ_311675 15345 RMVar_ID_15345 Human_SNP_ID_669470130 A-to-I Human chr19 + 53449744 53449744 53449744 AGTGTCTTGCTCTGTCACCCAGGGTAGAGTGCAATGGTGTGATCATGGCTCACTGCAGTCTTGAA AGTGTCTTGCTCTGTCACCCAGGGTAGAGTGCCATGGTGTGATCATGGCTCACTGCAGTCTTGAA A C AC022137.3,ZNF761 Ensembl:ENSG00000286261,Ensembl:ENSG00000160336 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1395982910 Functional Loss SNV dbSNP153 33..33 33 - - - 15346 RMVar_ID_15346 Human_SNP_ID_669470191 A-to-I Human chr19 + 53449962 53449962 53449962 GATCCTCCTCAGTCTCCCAAGTAGCTGAGATTACAGGTGCCAACCACCATACCTAATTATTGGCT GATCCTCCTCAGTCTCCCAAGTAGCTGAGATTTCAGGTGCCAACCACCATACCTAATTATTGGCT A T AC022137.3,ZNF761 Ensembl:ENSG00000286261,Ensembl:ENSG00000160336 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1474956310 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2041128,Human_Splice_Rec_2041144,Human_Splice_Rec_2041145 15347 RMVar_ID_15347 Human_SNP_ID_669470370 A-to-I Human chr19 + 53450209 53450209 53450209 CCTGTAATCCCAGCTACTTGGGAGGCTGAAGCAGGAGGATCACATGAACCTGGGAATCGGAGGTT CCTGTAATCCCAGCTACTTGGGAGGCTGAAGCCGGAGGATCACATGAACCTGGGAATCGGAGGTT A C AC022137.3,ZNF761 Ensembl:ENSG00000286261,Ensembl:ENSG00000160336 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1302519435 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6782775 15348 RMVar_ID_15348 Human_SNP_ID_669471120 A-to-I Human chr19 + 53453079 53453079 53453079 TCAACAATGCACAGGTGCAATCTCGGCTTACTACAACCTCCACTTCCTGGGTTCAAATGATTCTC TCAACAATGCACAGGTGCAATCTCGGCTTACTTCAACCTCCACTTCCTGGGTTCAAATGATTCTC A T AC022137.3,ZNF761 Ensembl:ENSG00000286261,Ensembl:ENSG00000160336 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs181170513 Functional Loss SNV dbSNP153 33..33 33 - - - 15349 RMVar_ID_15349 Human_SNP_ID_669471143 A-to-I Human chr19 + 53453187 53453187 53453187 CCACGACCAGCTAATTTTTTTGTATTTTTAGTAGAGTTGGGATTTCACCATGTTGGCCAAGCTAC CCACGACCAGCTAATTTTTTTGTATTTTTAGTGGAGTTGGGATTTCACCATGTTGGCCAAGCTAC A G AC022137.3,ZNF761 Ensembl:ENSG00000286261,Ensembl:ENSG00000160336 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1406677972 Functional Loss SNV dbSNP153 33..33 33 - - - 15350 RMVar_ID_15350 Human_SNP_ID_669481809 A-to-I Human chr19 + 53489187 53489187 53489187 GAGCCACCACACCCGGCTAATTTTGTATTGTTAGTAGAGACGGGGTTTCTCCATGTTTGTCAGGC GAGCCACCACACCCGGCTAATTTTGTATTGTTGGTAGAGACGGGGTTTCTCCATGTTTGTCAGGC A G ZNF813 Ensembl:ENSG00000198346 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1412294173 Functional Loss SNV dbSNP153 33..33 33 - - - 15351 RMVar_ID_15351 Human_SNP_ID_669483682 A-to-I Human chr19 + 53495405 53495405 53495405 GTGCCACCACATCAGCTAATTTTTGTATTTTTAGTAAGACGGGGTTTCACCATGTTGGCAAGGCT GTGCCACCACATCAGCTAATTTTTGTATTTTTTGTAAGACGGGGTTTCACCATGTTGGCAAGGCT A T ZNF813 Ensembl:ENSG00000198346 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs960037790 Functional Loss SNV dbSNP153 33..33 33 - - - 15352 RMVar_ID_15352 Human_SNP_ID_669502161 A-to-I Human chr19 + 53563109 53563106 53563109 GATTCCACACCCCCCCACCCCCCGTCCCCGAGAAGGAGTCTTGCTATGTCATCCAGGCTGGAGTG GATTCCACACCCCCCCACCCCCCGTCCCCG___AGGAGTCTTGCTATGTCATCCAGGCTGGAGTG GAGA G ZNF331 Ensembl:ENSG00000130844 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs550306331 Functional Loss DEL dbSNP153 31..33 33 - - - RMVar_hsa_circ_9624,RMVar_hsa_circ_347035,RMVar_hsa_circ_40425 15353 RMVar_ID_15353 Human_SNP_ID_669505003 A-to-I Human chr19 + 53573888 53573888 53573888 TAATCCCAGCACTTTGGGAGTCCAAGGCGGGCAGATCACCTGAAGTCAGGACTTCAAGACCAGCC TAATCCCAGCACTTTGGGAGTCCAAGGCGGGCGGATCACCTGAAGTCAGGACTTCAAGACCAGCC A G ZNF331 Ensembl:ENSG00000130844 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs748580795 Functional Loss SNV dbSNP153 33..33 33 - - - 15354 RMVar_ID_15354 Human_SNP_ID_669602996 A-to-I Human chr19 + 53875794 53875794 53875794 ATCCCTTCAACCCGGGAGGTGGAGGTTGCAGTAAGTCAAGATGGCACCACTGTGCTCCAGCCTGG ATCCCTTCAACCCGGGAGGTGGAGGTTGCAGTGAGTCAAGATGGCACCACTGTGCTCCAGCCTGG A G MYADM Ensembl:ENSG00000179820 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs11555355 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2229444,Human_miRNA_ID_2505415 RMVar_hsa_circ_104567,RMVar_hsa_circ_196212 15355 RMVar_ID_15355 Human_SNP_ID_669637221 A-to-I Human chr19 + 53987209 53987209 53987209 CCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCATGTGCCACCACGCCTGGCTAATTTTTTT CCTGCCTCAGCCTCCTGAGTAGCTGGGATTACGGGCATGTGCCACCACGCCTGGCTAATTTTTTT A G CACNG8 Ensembl:ENSG00000142408 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1379593319 Functional Loss SNV dbSNP153 33..33 33 - - - 15356 RMVar_ID_15356 Human_SNP_ID_669637565 A-to-I Human chr19 + 53988525 53988525 53988525 GAGAGGCTGAAGCAGGAGAATCTCTTGGGCCCAGGAGGCAGAGGTTGCAGTGAGCCAAGATCACA GAGAGGCTGAAGCAGGAGAATCTCTTGGGCCCGGGAGGCAGAGGTTGCAGTGAGCCAAGATCACA A G CACNG8 Ensembl:ENSG00000142408 Protein coding 3'UTR GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs566615714 Functional Loss SNV dbSNP153 33..33 33 - - - 15357 RMVar_ID_15357 Human_SNP_ID_669697519 A-to-I Human chr19 - 54175259 54175259 54175259 AGAACCACCGGGCTGCCCGGGTGTGGTGTCTGACACCTGTGATCCCAGCACTTTGGGAGGCCAAG AGAACCACCGGGCTGCCCGGGTGTGGTGTCTGGCACCTGTGATCCCAGCACTTTGGGAGGCCAAG T C MBOAT7 Ensembl:ENSG00000125505 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1389301561 Functional Loss SNV dbSNP153 33..33 33 - - - 15358 RMVar_ID_15358 Human_SNP_ID_669697633 A-to-I Human chr19 - 54175642 54175642 54175642 GGGAGGCTGAGGCATAAGAATCGCTTGAATCCAAGAGGCAGAGGCTGCAGTGAGCCTTGTCGTGT GGGAGGCTGAGGCATAAGAATCGCTTGAATCCGAGAGGCAGAGGCTGCAGTGAGCCTTGTCGTGT T C MBOAT7 Ensembl:ENSG00000125505 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1568779228 Functional Loss SNV dbSNP153 33..33 33 - - - 15359 RMVar_ID_15359 Human_SNP_ID_669697652 A-to-I Human chr19 - 54175687 54175687 54175687 AAATTAGCTGAGTTTGGTGGCGCTTGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCATAAGAA AAATTAGCTGAGTTTGGTGGCGCTTGCCTGTATTCCCAGCTACTTGGGAGGCTGAGGCATAAGAA T A MBOAT7 Ensembl:ENSG00000125505 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs757936463 Functional Loss SNV dbSNP153 33..33 33 - - - 15360 RMVar_ID_15360 Human_SNP_ID_669697894 A-to-I Human chr19 - 54176284 54176280 54176284 GTCCTCCCTTCTCAAGAAAACAAGAGTTGGCCAGGTGCAATGGCTGACATCTGTAATTCCAGTAT GTCCTCCCTTCTCAAGAAAACAAGAGTTGGCC____GCAATGGCTGACATCTGTAATTCCAGTAT CACCT C MBOAT7 Ensembl:ENSG00000125505 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1249314567 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_17567790 15361 RMVar_ID_15361 Human_SNP_ID_669697898 A-to-I Human chr19 - 54176284 54176284 54176284 GTCCTCCCTTCTCAAGAAAACAAGAGTTGGCCAGGTGCAATGGCTGACATCTGTAATTCCAGTAT GTCCTCCCTTCTCAAGAAAACAAGAGTTGGCCGGGTGCAATGGCTGACATCTGTAATTCCAGTAT T C MBOAT7 Ensembl:ENSG00000125505 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1253235530 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17567790 15362 RMVar_ID_15362 Human_SNP_ID_669697941 A-to-I Human chr19 - 54176436 54176436 54176436 CTCCTGTCTCAGCCCCCCTAGTAGCTGGGATTATAGGCACGTGCTACCATGACAGACTAATCTTT CTCCTGTCTCAGCCCCCCTAGTAGCTGGGATTGTAGGCACGTGCTACCATGACAGACTAATCTTT T C MBOAT7 Ensembl:ENSG00000125505 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs529829855 Functional Loss SNV dbSNP153 33..33 33 - - - 15363 RMVar_ID_15363 Human_SNP_ID_669700752 A-to-I Human chr19 - 54184169 54184157 54184169 ACAGAGCAAAACTTGTCTCAAAAAAAAAAAAAAAAAAAAAGAGAGAGAGATTAAAGGATCGGATT ACAGAGCAAAACTTGTCTCAAAAAAAAAAAAA____________GAGAGATTAAAGGATCGGATT CTCTCTTTTTTTT C MBOAT7 Ensembl:ENSG00000125505 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1422296556 Functional Loss DEL dbSNP153 33..44 33 - - - 15364 RMVar_ID_15364 Human_SNP_ID_669700801 A-to-I Human chr19 - 54184169 54184169 54184169 ACAGAGCAAAACTTGTCTCAAAAAAAAAAAAAAAAAAAAAGAGAGAGAGATTAAAGGATCGGATT ACAGAGCAAAACTTGTCTCAAAAAAAAAAAAAGAAAAAAAGAGAGAGAGATTAAAGGATCGGATT T C MBOAT7 Ensembl:ENSG00000125505 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1445740164 Functional Loss SNV dbSNP153 33..33 33 - - - 15365 RMVar_ID_15365 Human_SNP_ID_669701132 A-to-I Human chr19 - 54185277 54185277 54185277 ATAGTGGGAGGACTGCTGGAGGCCAGGAGTTTAAGACCAGCCTGGGCAATATAGTGAGACCCTGT ATAGTGGGAGGACTGCTGGAGGCCAGGAGTTTGAGACCAGCCTGGGCAATATAGTGAGACCCTGT T C MBOAT7 Ensembl:ENSG00000125505 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs573400273 Functional Loss SNV dbSNP153 33..33 33 - - - 15366 RMVar_ID_15366 Human_SNP_ID_669704942 A-to-I Human chr19 + 54194621 54194621 54194621 GTCTGGGCGTGGTGGCTTATGCTTGTAATCCCAGCACTTTGGGAGACCAAGGCGGGCGGATCATG GTCTGGGCGTGGTGGCTTATGCTTGTAATCCCGGCACTTTGGGAGACCAAGGCGGGCGGATCATG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1240903240 Functional Loss SNV dbSNP153 33..33 33 - - - 15367 RMVar_ID_15367 Human_SNP_ID_669707962 A-to-I Human chr19 + 54202134 54202134 54202134 ACCCCCGCCTCCTGGGTTCAAACAATTCTCCTATCTTAGCCTCCCAAGTAGCTGGGACTACAGAC ACCCCCGCCTCCTGGGTTCAAACAATTCTCCTGTCTTAGCCTCCCAAGTAGCTGGGACTACAGAC A G RPS9 Ensembl:ENSG00000170889 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1252216123 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17930801 RMVar_hsa_circ_103392,RMVar_hsa_circ_196228,RMVar_hsa_circ_196229,RMVar_hsa_circ_93060,RMVar_hsa_circ_269236 15368 RMVar_ID_15368 Human_SNP_ID_669708006 A-to-I Human chr19 + 54202249 54202244 54202250 CTCCATTGCCCATGCTGGAGTGTAGTTGTCGCAATCTTGGCTCACTGCAAACTCCGCCTCCAGAG CTCCATTGCCCATGCTGGAGTGTAGTTG______TCTTGGCTCACTGCAAACTCCGCCTCCAGAG GTCGCAA G RPS9 Ensembl:ENSG00000170889 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474136139 Functional Loss DEL dbSNP153 29..34 33 - - - Human_RBP_ID_13506558,Human_RBP_ID_23309956 RMVar_hsa_circ_103392,RMVar_hsa_circ_196228,RMVar_hsa_circ_196229,RMVar_hsa_circ_93060,RMVar_hsa_circ_269236 15369 RMVar_ID_15369 Human_SNP_ID_669708014 A-to-I Human chr19 + 54202249 54202249 54202249 CTCCATTGCCCATGCTGGAGTGTAGTTGTCGCAATCTTGGCTCACTGCAAACTCCGCCTCCAGAG CTCCATTGCCCATGCTGGAGTGTAGTTGTCGCGATCTTGGCTCACTGCAAACTCCGCCTCCAGAG A G RPS9 Ensembl:ENSG00000170889 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1019582813 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13506558,Human_RBP_ID_23309956 RMVar_hsa_circ_103392,RMVar_hsa_circ_196228,RMVar_hsa_circ_196229,RMVar_hsa_circ_93060,RMVar_hsa_circ_269236 15370 RMVar_ID_15370 Human_SNP_ID_669708029 A-to-I Human chr19 + 54202290 54202290 54202290 TCACTGCAAACTCCGCCTCCAGAGTTCAAGCGATTCTCCTGTCTTAGCCTCCTAAGTAGCTGGAA TCACTGCAAACTCCGCCTCCAGAGTTCAAGCGGTTCTCCTGTCTTAGCCTCCTAAGTAGCTGGAA A G RPS9 Ensembl:ENSG00000170889 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1032762504 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103392,RMVar_hsa_circ_196228,RMVar_hsa_circ_196229,RMVar_hsa_circ_93060,RMVar_hsa_circ_269236 15371 RMVar_ID_15371 Human_SNP_ID_669708235 A-to-I Human chr19 + 54202950 54202950 54202950 CAACTCCTAACCTCAAGTGATCCATCCACCTCAGCTTTCCAAAGTGCTGGGGTTACAGGTGTAAG CAACTCCTAACCTCAAGTGATCCATCCACCTCGGCTTTCCAAAGTGCTGGGGTTACAGGTGTAAG A G RPS9 Ensembl:ENSG00000170889 Protein coding intron GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 29796672,31158229,31158229 RNA-Seq:(High) rs1200846390 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13506604 RMVar_hsa_circ_103392,RMVar_hsa_circ_196228,RMVar_hsa_circ_196229,RMVar_hsa_circ_93060,RMVar_hsa_circ_269236 15372 RMVar_ID_15372 Human_SNP_ID_669708453 A-to-I Human chr19 + 54203648 54203648 54203648 TACAAAAATTAGCCGAGCATGGTGGTGTGCCTATAATCCCAGCTACTCGGGAGGCTGAGGCAGGA TACAAAAATTAGCCGAGCATGGTGGTGTGCCTCTAATCCCAGCTACTCGGGAGGCTGAGGCAGGA A C RPS9 Ensembl:ENSG00000170889 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1022380585 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103392,RMVar_hsa_circ_196228,RMVar_hsa_circ_196229,RMVar_hsa_circ_93060,RMVar_hsa_circ_269236 15373 RMVar_ID_15373 Human_SNP_ID_669708454 A-to-I Human chr19 + 54203648 54203648 54203648 TACAAAAATTAGCCGAGCATGGTGGTGTGCCTATAATCCCAGCTACTCGGGAGGCTGAGGCAGGA TACAAAAATTAGCCGAGCATGGTGGTGTGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGA A G RPS9 Ensembl:ENSG00000170889 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1022380585 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103392,RMVar_hsa_circ_196228,RMVar_hsa_circ_196229,RMVar_hsa_circ_93060,RMVar_hsa_circ_269236 15374 RMVar_ID_15374 Human_SNP_ID_669708467 A-to-I Human chr19 + 54203703 54203702 54203704 TGAGGCAGGAGAATTGATTGAACCTGGGAGACAGAGACTGCAGTGAGCCGAGATCCGCGGCACTG TGAGGCAGGAGAATTGATTGAACCTGGGAGAC__AGACTGCAGTGAGCCGAGATCCGCGGCACTG CAG C RPS9 Ensembl:ENSG00000170889 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs757097109 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_13506636 RMVar_hsa_circ_103392,RMVar_hsa_circ_196228,RMVar_hsa_circ_196229,RMVar_hsa_circ_93060,RMVar_hsa_circ_269236 15375 RMVar_ID_15375 Human_SNP_ID_669708626 A-to-I Human chr19 + 54204124 54204124 54204124 ATGTGGGCCTGAGTGCAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCAGAGGCAGGCGG ATGTGGGCCTGAGTGCAGTGGCTCATGCCTGTGATCCCAGCACTTTGGGAGGCAGAGGCAGGCGG A G RPS9 Ensembl:ENSG00000170889 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs935030083 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103392,RMVar_hsa_circ_196228,RMVar_hsa_circ_196229,RMVar_hsa_circ_93060,RMVar_hsa_circ_269236 15376 RMVar_ID_15376 Human_SNP_ID_669708745 A-to-I Human chr19 + 54204465 54204465 54204465 TCACTTTGTCTCCCGGGCTGGAGCACAGTGGCATGGTCGTGGCTCACTGCAGCCTGGACCTCCTG TCACTTTGTCTCCCGGGCTGGAGCACAGTGGCGTGGTCGTGGCTCACTGCAGCCTGGACCTCCTG A G RPS9 Ensembl:ENSG00000170889 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1392727001 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6783301,Human_RBP_ID_13506672,Human_RBP_ID_17568166 RMVar_hsa_circ_103392,RMVar_hsa_circ_196228,RMVar_hsa_circ_196229,RMVar_hsa_circ_93060,RMVar_hsa_circ_269236 15377 RMVar_ID_15377 Human_SNP_ID_669708798 A-to-I Human chr19 + 54204648 54204648 54204648 GTTGCCGAGGCTAGTTTCAAACTTCTGGACTCAACTGATCCTCCTGCCTCAGCCTCCCAAAATAT GTTGCCGAGGCTAGTTTCAAACTTCTGGACTCGACTGATCCTCCTGCCTCAGCCTCCCAAAATAT A G RPS9 Ensembl:ENSG00000170889 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs998910472 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17568771 RMVar_hsa_circ_103392,RMVar_hsa_circ_196228,RMVar_hsa_circ_196229,RMVar_hsa_circ_93060,RMVar_hsa_circ_269236 15378 RMVar_ID_15378 Human_SNP_ID_669709132 A-to-I Human chr19 + 54205848 54205844 54205848 TTTTGTATTGTTTTGTTTTGTGACAGGGCCTCACTCTGTCGCCCAGGCTGGAGTGCAGTGGCCCC TTTTGTATTGTTTTGTTTTGTGACAGGGC____CTCTGTCGCCCAGGCTGGAGTGCAGTGGCCCC CCTCA C RPS9 Ensembl:ENSG00000170889 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1484388366 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_13506747 RMVar_hsa_circ_103392,RMVar_hsa_circ_196228,RMVar_hsa_circ_196229,RMVar_hsa_circ_93060,RMVar_hsa_circ_269236 15379 RMVar_ID_15379 Human_SNP_ID_669784143 A-to-I Human chr19 - 54435268 54435268 54435268 AGCTGCACCCGCCCTTGTCATTGCAGGCCCCTATCTCCCTTTCACATGGGTCCTCCCCAGTCAGC AGCTGCACCCGCCCTTGTCATTGCAGGCCCCTGTCTCCCTTTCACATGGGTCCTCCCCAGTCAGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs534282681 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1295692,Human_RBP_ID_26995097 15380 RMVar_ID_15380 Human_SNP_ID_669785192 A-to-I Human chr19 - 54437902 54437902 54437902 GTGGTGCAACCTCCACCTCCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGC GTGGTGCAACCTCCACCTCCCGGGTTCAAGCATTTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGC T A LENG8-AS1 RNACentral:URS00009C1D5E lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs950293238 Functional Loss SNV dbSNP153 33..33 33 - - - 15381 RMVar_ID_15381 Human_SNP_ID_669785193 A-to-I Human chr19 - 54437902 54437902 54437902 GTGGTGCAACCTCCACCTCCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGC GTGGTGCAACCTCCACCTCCCGGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGC T C LENG8-AS1 RNACentral:URS00009C1D5E lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs950293238 Functional Loss SNV dbSNP153 33..33 33 - - - 15382 RMVar_ID_15382 Human_SNP_ID_669786685 A-to-I Human chr19 - 54443131 54443131 54443131 TTGCATTTTTAGTAGAGACAGGGTTTCACTATATTGGCTAGGCTGGTCTCAAACTCCTGACCTCG TTGCATTTTTAGTAGAGACAGGGTTTCACTATTTTGGCTAGGCTGGTCTCAAACTCCTGACCTCG T A LENG8-AS1,LENG8-AS1:2,LENG8-AS1:3,LENG8-AS1:4 RNACentral:URS0000D5B63F,RNACentral:URS00009B73B1,RNACentral:URS00009C0486,RNACentral:URS00009C1D5E lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1426631502 Functional Loss SNV dbSNP153 33..33 33 - - - 15383 RMVar_ID_15383 Human_SNP_ID_669786723 A-to-I Human chr19 - 54443240 54443240 54443240 ACAGTCTCGACTCACTGCAGCCTACTCCTCCCAGGTTCAAGCAGTTCTACTGCCTCAGCCTCCCA ACAGTCTCGACTCACTGCAGCCTACTCCTCCCGGGTTCAAGCAGTTCTACTGCCTCAGCCTCCCA T C LENG8-AS1,LENG8-AS1:2,LENG8-AS1:3,LENG8-AS1:4 RNACentral:URS0000D5B63F,RNACentral:URS00009B73B1,RNACentral:URS00009C0486,RNACentral:URS00009C1D5E lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1193938350 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13507465 15384 RMVar_ID_15384 Human_SNP_ID_669786729 A-to-I Human chr19 - 54443254 54443254 54443254 TGGAGTGCAGTGGCACAGTCTCGACTCACTGCAGCCTACTCCTCCCAGGTTCAAGCAGTTCTACT TGGAGTGCAGTGGCACAGTCTCGACTCACTGCTGCCTACTCCTCCCAGGTTCAAGCAGTTCTACT T A LENG8-AS1,LENG8-AS1:2,LENG8-AS1:3,LENG8-AS1:4 RNACentral:URS0000D5B63F,RNACentral:URS00009B73B1,RNACentral:URS00009C0486,RNACentral:URS00009C1D5E lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1201159403 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13507465 15385 RMVar_ID_15385 Human_SNP_ID_669787668 A-to-I Human chr19 - 54446314 54446314 54446314 GTTACTCATGAGGCTGAGGCAGGAGAATCGCTAGAACCCTGGGGGTGGAGGTTGCAGTGAGCCCA GTTACTCATGAGGCTGAGGCAGGAGAATCGCTTGAACCCTGGGGGTGGAGGTTGCAGTGAGCCCA T A LENG8-AS1 Ensembl:ENSG00000226696 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1257882867 Functional Loss SNV dbSNP153 33..33 33 - - - 15386 RMVar_ID_15386 Human_SNP_ID_669787669 A-to-I Human chr19 - 54446314 54446314 54446314 GTTACTCATGAGGCTGAGGCAGGAGAATCGCTAGAACCCTGGGGGTGGAGGTTGCAGTGAGCCCA GTTACTCATGAGGCTGAGGCAGGAGAATCGCTGGAACCCTGGGGGTGGAGGTTGCAGTGAGCCCA T C LENG8-AS1 Ensembl:ENSG00000226696 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1257882867 Functional Loss SNV dbSNP153 33..33 33 - - - 15387 RMVar_ID_15387 Human_SNP_ID_669787698 A-to-I Human chr19 - 54446420 54446420 54446420 CTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGGCGAAACCCCGTCTCTACTAAAAATACA CTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAGCATGGCGAAACCCCGTCTCTACTAAAAATACA T C LENG8-AS1 Ensembl:ENSG00000226696 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs950252715 Functional Loss SNV dbSNP153 33..33 33 - - - 15388 RMVar_ID_15388 Human_SNP_ID_669787764 A-to-I Human chr19 - 54446599 54446599 54446599 ACCTCAGGTGACCCGCCCGCCTCTGCCTCCCAAAGTGCCGGGATTACAGGCATGAGCCACTGCGC ACCTCAGGTGACCCGCCCGCCTCTGCCTCCCAGAGTGCCGGGATTACAGGCATGAGCCACTGCGC T C LENG8-AS1 Ensembl:ENSG00000226696 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1359135079 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22477280,Human_RBP_ID_22720511,Human_RBP_ID_23180275 15389 RMVar_ID_15389 Human_SNP_ID_669787791 A-to-I Human chr19 - 54446667 54446667 54446667 CACCACCACACCCAGCTAATTTTTGTATTTTTAGTGAAGACAGGGTTTCACAGTATCTGGAATTC CACCACCACACCCAGCTAATTTTTGTATTTTTGGTGAAGACAGGGTTTCACAGTATCTGGAATTC T C LENG8-AS1 Ensembl:ENSG00000226696 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1050796417 Functional Loss SNV dbSNP153 33..33 33 - - - 15390 RMVar_ID_15390 Human_SNP_ID_669787808 A-to-I Human chr19 - 54446741 54446741 54446741 GGAGTGCAGTAGCACGATCTCAGCTCACTGCAACCTTTGCCTCCCAGGTTCAAGCAATTCTCTTT GGAGTGCAGTAGCACGATCTCAGCTCACTGCAGCCTTTGCCTCCCAGGTTCAAGCAATTCTCTTT T C LENG8-AS1 Ensembl:ENSG00000226696 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005477020 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3588755 15391 RMVar_ID_15391 Human_SNP_ID_669987528 A-to-I Human chr19 - 55039472 55039447 55039473 GCGATCTCGGCTTACCGCAATCTCTGCCTCCCAGGTTCAAGCGATTCTCATGCCTCCGTCTCCCA GCGATCTCGGCTTACCGCAATCTCTGCCTCC__________________________GTCTCCCA CGGAGGCATGAGAATCGCTTGAACCTG C RDH13,AC011476.2 Ensembl:ENSG00000160439,Ensembl:ENSG00000267149 Protein coding,lincRNA intron,intron GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;Bronchiolar epithelium,BEP2D cell line - 29129909,30559470,31158229 RNA-Seq:(High) rs1442536590 Functional Loss DEL dbSNP153 32..57 33 - - - 15392 RMVar_ID_15392 Human_SNP_ID_669987543 A-to-I Human chr19 - 55039465 55039465 55039465 CGGCTTACCGCAATCTCTGCCTCCCAGGTTCAAGCGATTCTCATGCCTCCGTCTCCCAAGTAGCT CGGCTTACCGCAATCTCTGCCTCCCAGGTTCAGGCGATTCTCATGCCTCCGTCTCCCAAGTAGCT T C RDH13,AC011476.2 Ensembl:ENSG00000160439,Ensembl:ENSG00000267149 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1163626199 Functional Loss SNV dbSNP153 33..33 33 - - - 15393 RMVar_ID_15393 Human_SNP_ID_669987545 A-to-I Human chr19 - 55039472 55039472 55039472 GCGATCTCGGCTTACCGCAATCTCTGCCTCCCAGGTTCAAGCGATTCTCATGCCTCCGTCTCCCA GCGATCTCGGCTTACCGCAATCTCTGCCTCCCGGGTTCAAGCGATTCTCATGCCTCCGTCTCCCA T C RDH13,AC011476.2 Ensembl:ENSG00000160439,Ensembl:ENSG00000267149 Protein coding,lincRNA intron,intron GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;Bronchiolar epithelium,BEP2D cell line - 29129909,30559470,31158229 RNA-Seq:(High) rs1389751836 Functional Loss SNV dbSNP153 33..33 33 - - - 15394 RMVar_ID_15394 Human_SNP_ID_669987548 A-to-I Human chr19 - 55039485 55039485 55039485 GGAGTGCAGTGGTGCGATCTCGGCTTACCGCAATCTCTGCCTCCCAGGTTCAAGCGATTCTCATG GGAGTGCAGTGGTGCGATCTCGGCTTACCGCAGTCTCTGCCTCCCAGGTTCAAGCGATTCTCATG T C RDH13,AC011476.2 Ensembl:ENSG00000160439,Ensembl:ENSG00000267149 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs997654131 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13508077 15395 RMVar_ID_15395 Human_SNP_ID_669987910 A-to-I Human chr19 - 55040422 55040422 55040422 GGCACTGGCCGGGCGCGGTGGCTCATGCCTGTATTCCCAGCACTTTGGGAGGCCAAATCACAAGG GGCACTGGCCGGGCGCGGTGGCTCATGCCTGTGTTCCCAGCACTTTGGGAGGCCAAATCACAAGG T C RDH13,AC011476.2 Ensembl:ENSG00000160439,Ensembl:ENSG00000267149 Protein coding,lincRNA intron,intron GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 29129909,30559470 RNA-Seq:(High) rs1392315946 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5248813,Human_RBP_ID_23180293 15396 RMVar_ID_15396 Human_SNP_ID_669988074 A-to-I Human chr19 - 55040944 55040944 55040944 TTTTGTATTTTTAGTAGAGATGGCGTTTCTCCATGTTGGTCAGGCTGGTCTCAAACTCCCGACCT TTTTGTATTTTTAGTAGAGATGGCGTTTCTCCGTGTTGGTCAGGCTGGTCTCAAACTCCCGACCT T C RDH13,AC011476.2 Ensembl:ENSG00000160439,Ensembl:ENSG00000267149 Protein coding,lincRNA exon,intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1177806444 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_139063 15397 RMVar_ID_15397 Human_SNP_ID_669988607 A-to-I Human chr19 - 55042432 55042432 55042432 ACAGTGGCCAGGCGTGATGGTGCACGCCTGTAATCCCAGCTATTAGGGAGGCTGAGGCAGAAGAA ACAGTGGCCAGGCGTGATGGTGCACGCCTGTATTCCCAGCTATTAGGGAGGCTGAGGCAGAAGAA T A RDH13,AC011476.2 Ensembl:ENSG00000160439,Ensembl:ENSG00000267149 Protein coding,lincRNA exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs575188684 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23806952 15398 RMVar_ID_15398 Human_SNP_ID_669988847 A-to-I Human chr19 + 55043280 55043280 55043280 ATAATTAGCCAAGTGTGGTGGCATGCACCTGTAGTCCCAGATACTCAGGAGGCTGAGGCAGGAGA ATAATTAGCCAAGTGTGGTGGCATGCACCTGTTGTCCCAGATACTCAGGAGGCTGAGGCAGGAGA A T AC011476.3 Ensembl:ENSG00000267265 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1568673544 Functional Loss SNV dbSNP153 33..33 33 - - - 15399 RMVar_ID_15399 Human_SNP_ID_669988884 A-to-I Human chr19 - 55043380 55043380 55043380 TGCACCCAGCCCTTTTTGCTTTTTTAGAGACGAGGTCTTACTGTGTTGCCAAGGCTGGAGTGCAG TGCACCCAGCCCTTTTTGCTTTTTTAGAGACGTGGTCTTACTGTGTTGCCAAGGCTGGAGTGCAG T A RDH13,AC011476.2 Ensembl:ENSG00000160439,Ensembl:ENSG00000267149 Protein coding,lincRNA intron,intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs774088094 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13508187 15400 RMVar_ID_15400 Human_SNP_ID_669988966 A-to-I Human chr19 - 55043616 55043616 55043616 TTGCCCAGGCTGGAGTGCAATGGCATGATCTCAGCTCACTGCAACCTGTGTCTCCCATGTTCAAG TTGCCCAGGCTGGAGTGCAATGGCATGATCTCGGCTCACTGCAACCTGTGTCTCCCATGTTCAAG T C RDH13,AC011476.2 Ensembl:ENSG00000160439,Ensembl:ENSG00000267149 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900121104 Functional Loss SNV dbSNP153 33..33 33 - - - 15401 RMVar_ID_15401 Human_SNP_ID_670010153 A-to-I Human chr19 - 55101147 55101147 55101147 GTCCCCTGGGTTCAAGCAATTCTCCTGCCTCAACCTCCTGAGTAGCTGTGATTACAGGTGTGCTC GTCCCCTGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCTGTGATTACAGGTGTGCTC T C PPP1R12C Ensembl:ENSG00000125503 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs978546097 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5191809 RMVar_hsa_circ_78134,RMVar_hsa_circ_196256,RMVar_hsa_circ_109843,RMVar_hsa_circ_112308,RMVar_hsa_circ_196267,RMVar_hsa_circ_196268,RMVar_hsa_circ_196270,RMVar_hsa_circ_330329,RMVar_hsa_circ_298851 15402 RMVar_ID_15402 Human_SNP_ID_670011084 A-to-I Human chr19 - 55104458 55104458 55104458 CCTCAGGTGATCTGCCCACCTTGGTCTCCCAAAGTGTTGGGATTACAGGCATGAGCCGTTGTGCC CCTCAGGTGATCTGCCCACCTTGGTCTCCCAAGGTGTTGGGATTACAGGCATGAGCCGTTGTGCC T C PPP1R12C Ensembl:ENSG00000125503 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs576961204 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78134,RMVar_hsa_circ_196256,RMVar_hsa_circ_330329,RMVar_hsa_circ_121044,RMVar_hsa_circ_196271 15403 RMVar_ID_15403 Human_SNP_ID_670012150 A-to-I Human chr19 - 55108474 55108474 55108474 TTAGTGGGTACACATTTTTTAAAATGATTTTTATATTTTTTGTGGAGACGGGGTTTCACCACGTT TTAGTGGGTACACATTTTTTAAAATGATTTTTTTATTTTTTGTGGAGACGGGGTTTCACCACGTT T A PPP1R12C Ensembl:ENSG00000125503 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs537177691 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2570235,Human_RBP_ID_25433566 RMVar_hsa_circ_78134,RMVar_hsa_circ_196256,RMVar_hsa_circ_330329,RMVar_hsa_circ_121044,RMVar_hsa_circ_196271 15404 RMVar_ID_15404 Human_SNP_ID_670020064 A-to-I Human chr19 - 55134468 55134468 55134468 TTGCCCAGGCTGGTCTTGAACTCCTGGGCTCAAGTGTTCTGCTGGCCTCTGCCTCCCAAAGTGCT TTGCCCAGGCTGGTCTTGAACTCCTGGGCTCAGGTGTTCTGCTGGCCTCTGCCTCCCAAAGTGCT T C TNNT1 Ensembl:ENSG00000105048 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1362153466 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17568781 15405 RMVar_ID_15405 Human_SNP_ID_670020091 A-to-I Human chr19 - 55134593 55134593 55134593 GCAATCACAGCTCACTGCAGCTTTGACCTCCCAGGTTCCTTCTGCCTCAGCCTCCCAAGTAGCCG GCAATCACAGCTCACTGCAGCTTTGACCTCCCGGGTTCCTTCTGCCTCAGCCTCCCAAGTAGCCG T C TNNT1 Ensembl:ENSG00000105048 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1047810162 Functional Loss SNV dbSNP153 33..33 33 - - - 15406 RMVar_ID_15406 Human_SNP_ID_670022475 A-to-I Human chr19 - 55141612 55141612 55141612 GGGCGTGGTGGCAGGTGTCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAAAATCGCTTGAA GGGCGTGGTGGCAGGTGTCTGTAATCCCAGCTGCTCGGGAGGCTGAGGCAGGAAAATCGCTTGAA T C TNNT1 Ensembl:ENSG00000105048 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1227977426 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25433628 RMVar_hsa_circ_31035,RMVar_hsa_circ_322550 15407 RMVar_ID_15407 Human_SNP_ID_670022477 A-to-I Human chr19 - 55141622 55141622 55141622 AAAATTAGCCGGGCGTGGTGGCAGGTGTCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAAA AAAATTAGCCGGGCGTGGTGGCAGGTGTCTGTGATCCCAGCTACTCGGGAGGCTGAGGCAGGAAA T C TNNT1 Ensembl:ENSG00000105048 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1284308586 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_31035,RMVar_hsa_circ_322550 15408 RMVar_ID_15408 Human_SNP_ID_670022481 A-to-I Human chr19 - 55141632 55141632 55141632 TAAAAATACAAAAATTAGCCGGGCGTGGTGGCAGGTGTCTGTAATCCCAGCTACTCGGGAGGCTG TAAAAATACAAAAATTAGCCGGGCGTGGTGGCGGGTGTCTGTAATCCCAGCTACTCGGGAGGCTG T C TNNT1 Ensembl:ENSG00000105048 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1394810999 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_31035,RMVar_hsa_circ_322550 15409 RMVar_ID_15409 Human_SNP_ID_670022492 A-to-I Human chr19 - 55141652 55141650 55141652 TGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCCGGGCGTGGTGGCAGGTGTCTGTAAT TGGTGAAACCCCGTCTCTACTAAAAATACAAA__TTAGCCGGGCGTGGTGGCAGGTGTCTGTAAT ATT A TNNT1 Ensembl:ENSG00000105048 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs982408159 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_31035,RMVar_hsa_circ_322550 15410 RMVar_ID_15410 Human_SNP_ID_670057340 A-to-I Human chr19 - 55243483 55243483 55243483 TTTTTTTGTATTTGTAGAGATAGAGTTTTGCTATGTTGCCCCGACTGGTCTCAAACTCCTGGGCT TTTTTTTGTATTTGTAGAGATAGAGTTTTGCTGTGTTGCCCCGACTGGTCTCAAACTCCTGGGCT T C PPP6R1 Ensembl:ENSG00000105063 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1031464550 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123810,RMVar_hsa_circ_101499,RMVar_hsa_circ_196285,RMVar_hsa_circ_19427,RMVar_hsa_circ_196284,RMVar_hsa_circ_85532,RMVar_hsa_circ_99208,RMVar_hsa_circ_342371,RMVar_hsa_circ_93017,RMVar_hsa_circ_196295,RMVar_hsa_circ_196296,RMVar_hsa_circ_196300,RMVar_hsa_circ_332560 15411 RMVar_ID_15411 Human_SNP_ID_670057347 A-to-I Human chr19 - 55243500 55243500 55243500 CCACCATTCTTGGCTAATTTTTTTGTATTTGTAGAGATAGAGTTTTGCTATGTTGCCCCGACTGG CCACCATTCTTGGCTAATTTTTTTGTATTTGTGGAGATAGAGTTTTGCTATGTTGCCCCGACTGG T C PPP6R1 Ensembl:ENSG00000105063 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1329575544 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123810,RMVar_hsa_circ_101499,RMVar_hsa_circ_196285,RMVar_hsa_circ_19427,RMVar_hsa_circ_196284,RMVar_hsa_circ_85532,RMVar_hsa_circ_99208,RMVar_hsa_circ_342371,RMVar_hsa_circ_93017,RMVar_hsa_circ_196295,RMVar_hsa_circ_196296,RMVar_hsa_circ_196300,RMVar_hsa_circ_332560 15412 RMVar_ID_15412 Human_SNP_ID_670057744 A-to-I Human chr19 - 55244823 55244823 55244823 AGGAGGATTGCTTGAGCCGGGAGGTCAAGGCTATAGTGAGTCATGATCACACCACTGCACTCCAG AGGAGGATTGCTTGAGCCGGGAGGTCAAGGCTGTAGTGAGTCATGATCACACCACTGCACTCCAG T C PPP6R1 Ensembl:ENSG00000105063 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1181890027 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123810,RMVar_hsa_circ_101499,RMVar_hsa_circ_196285,RMVar_hsa_circ_19427,RMVar_hsa_circ_196284,RMVar_hsa_circ_85532,RMVar_hsa_circ_99208,RMVar_hsa_circ_342371,RMVar_hsa_circ_93017,RMVar_hsa_circ_196295,RMVar_hsa_circ_196296,RMVar_hsa_circ_196300,RMVar_hsa_circ_332560 15413 RMVar_ID_15413 Human_SNP_ID_670057803 A-to-I Human chr19 - 55245027 55245027 55245027 CCACTTTTAAAAGAGGAATTGGGGCTGGACGCAGTGGCTCACGCCTGTAATTCCAGCACTTTGGG CCACTTTTAAAAGAGGAATTGGGGCTGGACGCGGTGGCTCACGCCTGTAATTCCAGCACTTTGGG T C PPP6R1 Ensembl:ENSG00000105063 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1228546669 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5372189,Human_RBP_ID_22594512 RMVar_hsa_circ_123810,RMVar_hsa_circ_101499,RMVar_hsa_circ_196285,RMVar_hsa_circ_19427,RMVar_hsa_circ_196284,RMVar_hsa_circ_85532,RMVar_hsa_circ_99208,RMVar_hsa_circ_342371,RMVar_hsa_circ_93017,RMVar_hsa_circ_196295,RMVar_hsa_circ_196296,RMVar_hsa_circ_196300,RMVar_hsa_circ_332560 15414 RMVar_ID_15414 Human_SNP_ID_670102710 A-to-I Human chr19 - 55388368 55388368 55388368 CAAAAAGGGAGGCCCAGTCGAGGCAGGTGAGAAAGCCAGCTGACTTTATTGCTCTGGGGGCAGGG CAAAAAGGGAGGCCCAGTCGAGGCAGGTGAGACAGCCAGCTGACTTTATTGCTCTGGGGGCAGGG T G - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1392270437 Functional Loss SNV dbSNP153 33..33 33 - - - 15415 RMVar_ID_15415 Human_SNP_ID_670102971 A-to-I Human chr19 + 55389174 55389171 55389174 GGCCAGGAGTTTGAGACCATCCTAGGCAACATAATGAGACACCGTCTCTAAAATAAAATTAGCTG GGCCAGGAGTTTGAGACCATCCTAGGCAAC___ATGAGACACCGTCTCTAAAATAAAATTAGCTG CATA C RPL28 Ensembl:ENSG00000108107 Protein coding intron GSE47997;GSE38233;GSE38233;GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,24183664,29129909,32596459 RNA-Seq:(High) rs113573419 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_17930972,Human_RBP_ID_26472899 RMVar_hsa_circ_98465,RMVar_hsa_circ_196328 15416 RMVar_ID_15416 Human_SNP_ID_670103430 A-to-I Human chr19 + 55390405 55390405 55390405 TATTGTATTTTTAGCAGAGATGGGGTTTCACCATTTTGCCCAGGCTGGTTTGGAACTCCTGACTT TATTGTATTTTTAGCAGAGATGGGGTTTCACCGTTTTGCCCAGGCTGGTTTGGAACTCCTGACTT A G RPL28 Ensembl:ENSG00000108107 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1385072814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13509673,Human_RBP_ID_26472905,Human_RBP_ID_26995387,Human_RBP_ID_27471358 Human_miRNA_ID_1658364,Human_miRNA_ID_2247780,Human_miRNA_ID_2852090 RMVar_hsa_circ_98465,RMVar_hsa_circ_196328 15417 RMVar_ID_15417 Human_SNP_ID_670104702 A-to-I Human chr19 + 55394363 55394363 55394363 CTCACTGCAGCCTTGAACTCCTGGGCTCAAACAATCCTCCCACCTCAGTCTCCGAAGTAGCTGGC CTCACTGCAGCCTTGAACTCCTGGGCTCAAACGATCCTCCCACCTCAGTCTCCGAAGTAGCTGGC A G RPL28 Ensembl:ENSG00000108107 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs772010763 Functional Loss SNV dbSNP153 33..33 33 - - - 15418 RMVar_ID_15418 Human_SNP_ID_670108421 A-to-I Human chr19 - 55405153 55405153 55405153 CAGGCTGGAGTGCAGTGGCGCGATCTCCGCACACTGCAACCTCCCCATCCCGGGTTCAAGGGATT CAGGCTGGAGTGCAGTGGCGCGATCTCCGCACGCTGCAACCTCCCCATCCCGGGTTCAAGGGATT T C UBE2S Ensembl:ENSG00000108106 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1171949900 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87339,RMVar_hsa_circ_90663,RMVar_hsa_circ_196334,RMVar_hsa_circ_196335 15419 RMVar_ID_15419 Human_SNP_ID_670110878 A-to-I Human chr19 + 55413304 55413304 55413304 AACTCGAGAGATGGAGGTTGCAGTGAGCCGAGATTGTGCCACTGCACTCCAGCCTGGGCCACAGA AACTCGAGAGATGGAGGTTGCAGTGAGCCGAGTTTGTGCCACTGCACTCCAGCCTGGGCCACAGA A T lnc-RPL28-1-002 RNACentral:URS00008BE546 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs963769726 Functional Loss SNV dbSNP153 33..33 33 - - - 15420 RMVar_ID_15420 Human_SNP_ID_670111062 A-to-I Human chr19 + 55413744 55413744 55413744 TTACTCTGTCACCCAGGCTGTAGTGCAGTGGCATGATCTCATCTCACTGCAGCCTCCACCTCCCA TTACTCTGTCACCCAGGCTGTAGTGCAGTGGCGTGATCTCATCTCACTGCAGCCTCCACCTCCCA A G lnc-RPL28-1-002 RNACentral:URS00008BE546 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1347468513 Functional Loss SNV dbSNP153 33..33 33 - - - 15421 RMVar_ID_15421 Human_SNP_ID_670174418 A-to-I Human chr19 + 55610495 55610495 55610495 GTAGGCCAGACTGGTGTCGAACTCCTAACCTCAGGTGATCCTCCTGCCTTGGCCTCCCAAAGTGC GTAGGCCAGACTGGTGTCGAACTCCTAACCTCGGGTGATCCTCCTGCCTTGGCCTCCCAAAGTGC A G ZNF865 Ensembl:ENSG00000261221 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1003049222 Functional Loss SNV dbSNP153 33..33 33 - - - 15422 RMVar_ID_15422 Human_SNP_ID_670182446 A-to-I Human chr19 + 55637080 55637080 55637080 GGCTCAGGCAATCCTGTCTCAGCTTCCTGGGTAGTTGGGACTGTAGGCAGGCACCACCACCTCTG GGCTCAGGCAATCCTGTCTCAGCTTCCTGGGTGGTTGGGACTGTAGGCAGGCACCACCACCTCTG A G ZNF580,ZNF581 Ensembl:ENSG00000213015,Ensembl:ENSG00000171425 Protein coding,Protein coding intron,intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs758423994 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6784272,Human_RBP_ID_13510888 RMVar_hsa_circ_78319,RMVar_hsa_circ_196349 15423 RMVar_ID_15423 Human_SNP_ID_670182829 A-to-I Human chr19 + 55638496 55638496 55638496 TGACCTCGTAATCTGCCCGCCTCGCCCTCCCAAAGTGTTGGGATTACAGGCGTGAGCCACCACGC TGACCTCGTAATCTGCCCGCCTCGCCCTCCCAGAGTGTTGGGATTACAGGCGTGAGCCACCACGC A G ZNF580,ZNF581 Ensembl:ENSG00000213015,Ensembl:ENSG00000171425 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1235917533 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23180343 RMVar_hsa_circ_78319,RMVar_hsa_circ_196349 15424 RMVar_ID_15424 Human_SNP_ID_670205343 A-to-I Human chr19 + 55701338 55701338 55701338 TAGTGTGGTGGCGGGCACCTGTAATCCCAGCTACTTAGGAGGCTGAGGCAGGAGAATCGCTTGAA TAGTGTGGTGGCGGGCACCTGTAATCCCAGCTGCTTAGGAGGCTGAGGCAGGAGAATCGCTTGAA A G EPN1 Ensembl:ENSG00000063245 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1289303014 Functional Loss SNV dbSNP153 33..33 33 - - - 15425 RMVar_ID_15425 Human_SNP_ID_670207378 A-to-I Human chr19 - 55705858 55705854 55705858 AGCTTTAGTGATAGAGCAAGACCTTGTCTCTAAATATATATATATATCCCACAACACTCTAAATA AGCTTTAGTGATAGAGCAAGACCTTGTCTCTA____TATATATATATCCCACAACACTCTAAATA ATATT A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1288712029 Functional Loss DEL dbSNP153 33..36 33 - - - 15426 RMVar_ID_15426 Human_SNP_ID_670207380 A-to-I Human chr19 - 55705858 55705856 55705858 AGCTTTAGTGATAGAGCAAGACCTTGTCTCTAAATATATATATATATCCCACAACACTCTAAATA AGCTTTAGTGATAGAGCAAGACCTTGTCTCTA__TATATATATATATCCCACAACACTCTAAATA ATT A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs778366626 Functional Loss DEL dbSNP153 33..34 33 - - - 15427 RMVar_ID_15427 Human_SNP_ID_670207381 A-to-I Human chr19 - 55705858 55705858 55705858 AGCTTTAGTGATAGAGCAAGACCTTGTCTCTAAATATATATATATATCCCACAACACTCTAAATA AGCTTTAGTGATAGAGCAAGACCTTGTCTCTATATATATATATATATCCCACAACACTCTAAATA T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs536467064 Functional Loss SNV dbSNP153 33..33 33 - - - 15428 RMVar_ID_15428 Human_SNP_ID_670207382 A-to-I Human chr19 - 55705858 55705858 55705858 AGCTTTAGTGATAGAGCAAGACCTTGTCTCTAAATATATATATATATCCCACAACACTCTAAATA AGCTTTAGTGATAGAGCAAGACCTTGTCTCTAGATATATATATATATCCCACAACACTCTAAATA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs536467064 Functional Loss SNV dbSNP153 33..33 33 - - - 15429 RMVar_ID_15429 Human_SNP_ID_670390526 A-to-I Human chr19 - 56264959 56264959 56264959 TGCCACCACACCTGGCTAATTTTTGTATTTGTAGTAGATACGGGGTTTCACCATGTCTGCCAGGC TGCCACCACACCTGGCTAATTTTTGTATTTGTGGTAGATACGGGGTTTCACCATGTCTGCCAGGC T C ZSCAN5A Ensembl:ENSG00000131848 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs995738212 Functional Loss SNV dbSNP153 33..33 33 - - - 15430 RMVar_ID_15430 Human_SNP_ID_670398786 A-to-I Human chr19 - 56299194 56299194 56299194 CTAGGAGTTTAGGGCTGTGGTGAGCCGTGATCATACCACTGCACTCCAGCCTGGGCAACAAAGCT CTAGGAGTTTAGGGCTGTGGTGAGCCGTGATCGTACCACTGCACTCCAGCCTGGGCAACAAAGCT T C ZSCAN5A Ensembl:ENSG00000131848 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1262654564 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25434816 15431 RMVar_ID_15431 Human_SNP_ID_670418303 A-to-I Human chr19 + 56378584 56378584 56378584 ACAATCATGGCTCACTGCAGTCTCTGCCTCCCAGGCTCAAGTGATCCTCCCACCTCAGCCTCTCA ACAATCATGGCTCACTGCAGTCTCTGCCTCCCGGGCTCAAGTGATCCTCCCACCTCAGCCTCTCA A G ZNF542P Ensembl:ENSG00000240225 Pseudogene exon GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1009055195 Functional Loss SNV dbSNP153 33..33 33 - - - 15432 RMVar_ID_15432 Human_SNP_ID_670418339 A-to-I Human chr19 + 56378748 56378746 56378748 AGCTCAAGCAGTCCATCTGCCTCAGCCTCCCAAAGTGCTGGGACTACAGACATGAGCCATTGTGC AGCTCAAGCAGTCCATCTGCCTCAGCCTCCC__AGTGCTGGGACTACAGACATGAGCCATTGTGC CAA C ZNF542P Ensembl:ENSG00000240225 Pseudogene exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs996367239 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_9929881,Human_RBP_ID_17502681 15433 RMVar_ID_15433 Human_SNP_ID_670418339 A-to-I Human chr19 + 56378747 56378746 56378748 GAGCTCAAGCAGTCCATCTGCCTCAGCCTCCCAAAGTGCTGGGACTACAGACATGAGCCATTGTG GAGCTCAAGCAGTCCATCTGCCTCAGCCTCCC__AGTGCTGGGACTACAGACATGAGCCATTGTG CAA C ZNF542P Ensembl:ENSG00000240225 Pseudogene exon GSE47997;GSE107867 K562 cells&HepG2 cells;ASD brains,cerebellum - 23474544,30559470 RNA-Seq:(High) rs996367239 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_9929881,Human_RBP_ID_17502681 15434 RMVar_ID_15434 Human_SNP_ID_670642822 A-to-I Human chr19 + 57214562 57214562 57214562 TTTGGTAGAGACAGGGTTTCACCATGGTGCCCAGGCTGGTCTTGAACTCCTGGGCTCAAGCAACC TTTGGTAGAGACAGGGTTTCACCATGGTGCCCCGGCTGGTCTTGAACTCCTGGGCTCAAGCAACC A C ZNF264 Ensembl:ENSG00000083844 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934725438 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196396,RMVar_hsa_circ_116332,RMVar_hsa_circ_196395 15435 RMVar_ID_15435 Human_SNP_ID_670642837 A-to-I Human chr19 + 57214613 57214613 57214613 GGGCTCAAGCAACCTGCTTGCCTGGGTCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACAGTG GGGCTCAAGCAACCTGCTTGCCTGGGTCTCCCCAAGTGCTGGGATTACAGGCGTGAGCCACAGTG A C ZNF264 Ensembl:ENSG00000083844 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1393186950 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196396,RMVar_hsa_circ_116332,RMVar_hsa_circ_196395 15436 RMVar_ID_15436 Human_SNP_ID_670643202 A-to-I Human chr19 + 57216209 57216209 57216209 AACCCTGTCTACTAAAAATACAAAAATTAGCCAGGCATGGTGGCGTGTGCCTGTAATCCCAGCTG AACCCTGTCTACTAAAAATACAAAAATTAGCCGGGCATGGTGGCGTGTGCCTGTAATCCCAGCTG A G ZNF264 Ensembl:ENSG00000083844 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs780812005 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196396,RMVar_hsa_circ_116332,RMVar_hsa_circ_196395 15437 RMVar_ID_15437 Human_SNP_ID_670643527 A-to-I Human chr19 + 57217497 57217497 57217497 TGGAGTGCTGTGATGCGATCTCGGCTCTCTGCAACCTCTGCCTCCCGGGTTCAAGCAATTAACTG TGGAGTGCTGTGATGCGATCTCGGCTCTCTGCTACCTCTGCCTCCCGGGTTCAAGCAATTAACTG A T ZNF264 Ensembl:ENSG00000083844 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1555766653 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13517164 Human_miRNA_ID_2274075,Human_miRNA_ID_2476787,Human_miRNA_ID_2962568 RMVar_hsa_circ_196396,RMVar_hsa_circ_116332,RMVar_hsa_circ_196395 15438 RMVar_ID_15438 Human_SNP_ID_670643698 A-to-I Human chr19 + 57217953 57217953 57217953 AGCTGGGATTACAGGTGTGCGCCGCCACACCCAGCTAATTTTGTATTTTTAGTAGAGACGGGGTT AGCTGGGATTACAGGTGTGCGCCGCCACACCCGGCTAATTTTGTATTTTTAGTAGAGACGGGGTT A G ZNF264 Ensembl:ENSG00000083844 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs990974156 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196396,RMVar_hsa_circ_116332,RMVar_hsa_circ_196395 15439 RMVar_ID_15439 Human_SNP_ID_670643706 A-to-I Human chr19 + 57217988 57217988 57217988 TAATTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGCTCAGGCTGGTCTCAAACTCCTGA TAATTTTGTATTTTTAGTAGAGACGGGGTTTCGCCATGTTGCTCAGGCTGGTCTCAAACTCCTGA A G ZNF264 Ensembl:ENSG00000083844 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs1414582610 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196396,RMVar_hsa_circ_116332,RMVar_hsa_circ_196395 15440 RMVar_ID_15440 Human_SNP_ID_670643712 A-to-I Human chr19 + 57218011 57218011 57218011 CGGGGTTTCACCATGTTGCTCAGGCTGGTCTCAAACTCCTGACCTTGTGATCCGCCAACCTTGGC CGGGGTTTCACCATGTTGCTCAGGCTGGTCTCGAACTCCTGACCTTGTGATCCGCCAACCTTGGC A G ZNF264 Ensembl:ENSG00000083844 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1480087313 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196396,RMVar_hsa_circ_116332,RMVar_hsa_circ_196395 15441 RMVar_ID_15441 Human_SNP_ID_670644356 A-to-I Human chr19 + 57220712 57220712 57220712 CCACCCAGACTGAAGTGCAGTGGTGCGATCTCAGTTCACTGCAACCTCCATCCCCCCATGTTCAA CCACCCAGACTGAAGTGCAGTGGTGCGATCTCGGTTCACTGCAACCTCCATCCCCCCATGTTCAA A G ZNF264 Ensembl:ENSG00000083844 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1279027276 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196396,RMVar_hsa_circ_116332,RMVar_hsa_circ_196395 15442 RMVar_ID_15442 Human_SNP_ID_670644366 A-to-I Human chr19 + 57220743 57220743 57220743 CAGTTCACTGCAACCTCCATCCCCCCATGTTCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGC CAGTTCACTGCAACCTCCATCCCCCCATGTTCCAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGC A C ZNF264 Ensembl:ENSG00000083844 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1007995865 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196396,RMVar_hsa_circ_116332,RMVar_hsa_circ_196395 15443 RMVar_ID_15443 Human_SNP_ID_670644388 A-to-I Human chr19 + 57220827 57220827 57220827 CACCATGCCCGGCTAATTTTTGTATTTTTTGTAGACACGGGGTTTCACCATGTTGGCCAGGCTGG CACCATGCCCGGCTAATTTTTGTATTTTTTGTGGACACGGGGTTTCACCATGTTGGCCAGGCTGG A G ZNF264 Ensembl:ENSG00000083844 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs1357458647 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196396,RMVar_hsa_circ_116332,RMVar_hsa_circ_196395 15444 RMVar_ID_15444 Human_SNP_ID_670644419 A-to-I Human chr19 + 57220915 57220915 57220915 ATCCACCCGCCTCGGCCTCCCGAAGTGCTGGCATTACAGGCATGAGCCACCACACCCAGCCTTTA ATCCACCCGCCTCGGCCTCCCGAAGTGCTGGCGTTACAGGCATGAGCCACCACACCCAGCCTTTA A G ZNF264 Ensembl:ENSG00000083844 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs533496714 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196396,RMVar_hsa_circ_116332,RMVar_hsa_circ_196395 15445 RMVar_ID_15445 Human_SNP_ID_670644474 A-to-I Human chr19 + 57221127 57221127 57221127 TGCTGGTGTGCAGTGGCGTGATCTTGGCTCACAGCAGCCTCTGCCTCCCGGGTTCAAGCGATTCT TGCTGGTGTGCAGTGGCGTGATCTTGGCTCACGGCAGCCTCTGCCTCCCGGGTTCAAGCGATTCT A G ZNF264 Ensembl:ENSG00000083844 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1218248454 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1345664,Human_miRNA_ID_2274076,Human_miRNA_ID_2476788,Human_miRNA_ID_2673482,Human_miRNA_ID_2716455,Human_miRNA_ID_2962569,Human_miRNA_ID_3052439 RMVar_hsa_circ_196396,RMVar_hsa_circ_116332,RMVar_hsa_circ_196395 15446 RMVar_ID_15446 Human_SNP_ID_670644535 A-to-I Human chr19 + 57221310 57221310 57221310 TGACTTCATGATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCAC TGACTTCATGATCCACCCGCCTCGGCCTCCCAGAGTGCTGGGATTACAGGCGTGAGCCACCGCAC A G ZNF264 Ensembl:ENSG00000083844 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs943173839 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196396,RMVar_hsa_circ_116332,RMVar_hsa_circ_196395 15447 RMVar_ID_15447 Human_SNP_ID_670645107 A-to-I Human chr19 + 57223174 57223174 57223174 GAAACACTGCCTTGGGCGCCCAGTGTTGGATTACAGGTGTGAGCCACCACACCCAGGCTGTATTG GAAACACTGCCTTGGGCGCCCAGTGTTGGATTGCAGGTGTGAGCCACCACACCCAGGCTGTATTG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1245527162 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196396,RMVar_hsa_circ_116332,RMVar_hsa_circ_196395 15448 RMVar_ID_15448 Human_SNP_ID_670646567 A-to-I Human chr19 + 57228991 57228991 57228991 TTGGAATTAAAAGGTCCCCGAGGGCCAGGGACAGTGGCTCACGCCTGTAATCCCAGCAATTTGGG TTGGAATTAAAAGGTCCCCGAGGGCCAGGGACCGTGGCTCACGCCTGTAATCCCAGCAATTTGGG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251955894 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196396,RMVar_hsa_circ_116332,RMVar_hsa_circ_196395 15449 RMVar_ID_15449 Human_SNP_ID_670657383 A-to-I Human chr19 - 57269350 57269350 57269350 GCATGTGCCACCATGCCCGGGTAATTTTTTGTATTTTTAGTAGAGACAGGGTTTCACCGTGTTAG GCATGTGCCACCATGCCCGGGTAATTTTTTGTGTTTTTAGTAGAGACAGGGTTTCACCGTGTTAG T C ZNF460-AS1 Ensembl:ENSG00000267871 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs974581326 Functional Loss SNV dbSNP153 33..33 33 - - - 15450 RMVar_ID_15450 Human_SNP_ID_670661131 A-to-I Human chr19 + 57282844 57282844 57282844 AAACCCTGTCTCTACAAAAAGTACAAAAAATTAGACCGGCATGGCATCATGTGCCTGTAGTCCCA AAACCCTGTCTCTACAAAAAGTACAAAAAATTGGACCGGCATGGCATCATGTGCCTGTAGTCCCA A G ZNF460 Ensembl:ENSG00000197714 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs948523249 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196399,RMVar_hsa_circ_87432,RMVar_hsa_circ_196400 15451 RMVar_ID_15451 Human_SNP_ID_670661314 A-to-I Human chr19 + 57283303 57283303 57283303 GCGATTCTCCTGCTTCAGCCTCCCGAGTAGCTAGGACTACAGGCACACACTACCACACCCAGCTA GCGATTCTCCTGCTTCAGCCTCCCGAGTAGCTGGGACTACAGGCACACACTACCACACCCAGCTA A G ZNF460 Ensembl:ENSG00000197714 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs572645856 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196399,RMVar_hsa_circ_87432,RMVar_hsa_circ_196400 15452 RMVar_ID_15452 Human_SNP_ID_670663035 A-to-I Human chr19 + 57289916 57289916 57289916 TAATTCTAGCATTTTGGAAGGCCGAGGCAGGCAGATCACCTGAGTTCAGGGGTTCTAGACCAGTC TAATTCTAGCATTTTGGAAGGCCGAGGCAGGCGGATCACCTGAGTTCAGGGGTTCTAGACCAGTC A G ZNF460 Ensembl:ENSG00000197714 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1293513254 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196399,RMVar_hsa_circ_87432,RMVar_hsa_circ_196400 15453 RMVar_ID_15453 Human_SNP_ID_670665387 A-to-I Human chr19 + 57298570 57298570 57298570 TTGGCTCACTGCAACCTCTGACTCCTGGGTTTAAGCATTTCTCCTGCCTCACCCTCCCGAGTAGC TTGGCTCACTGCAACCTCTGACTCCTGGGTTTGAGCATTTCTCCTGCCTCACCCTCCCGAGTAGC A G lnc-ZNF460-1 RNACentral:URS00008BF31C lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1261247178 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1018408,Human_RBP_ID_2571014,Human_RBP_ID_13518219,Human_RBP_ID_17385730,Human_RBP_ID_24485001 RMVar_hsa_circ_196399 15454 RMVar_ID_15454 Human_SNP_ID_670666051 A-to-I Human chr19 + 57301174 57301174 57301174 GTCTTGAACTCCTGACCTCAAGTGACTCGCCCACCTTGGTGTCCTAAAGTGCTGGAATTACAGGT GTCTTGAACTCCTGACCTCAAGTGACTCGCCCGCCTTGGTGTCCTAAAGTGCTGGAATTACAGGT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1205600812 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_527841,Human_RBP_ID_6787419,Human_RBP_ID_9090026,Human_RBP_ID_13518381,Human_RBP_ID_17931884,Human_RBP_ID_18740296,Human_RBP_ID_23808741,Human_RBP_ID_27683323 RMVar_hsa_circ_196399 15455 RMVar_ID_15455 Human_SNP_ID_670666720 A-to-I Human chr19 + 57304082 57304082 57304082 GGGATTACAGGCCCCCACCACAACGCCCAGCTAATTTTTTTATTTTTTGTAGAGATGGGGTTTCA GGGATTACAGGCCCCCACCACAACGCCCAGCTGATTTTTTTATTTTTTGTAGAGATGGGGTTTCA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1008331601 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_527884,Human_RBP_ID_6787592,Human_RBP_ID_17931928 RMVar_hsa_circ_196399 15456 RMVar_ID_15456 Human_SNP_ID_670666906 A-to-I Human chr19 + 57304784 57304784 57304784 AAAGATTTAAAACACTTTCGGCCGGGCGCGGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGTGG AAAGATTTAAAACACTTTCGGCCGGGCGCGGTGATCCCAGCACTTTGGGAGGCCGAGGCGGGTGG A G AC005261.1 Ensembl:ENSG00000268205 lincRNA exon GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1568504006 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6787622,Human_RBP_ID_13518635 Human_miRNA_ID_3146651,Human_miRNA_ID_3146885,Human_miRNA_ID_3154933,Human_miRNA_ID_3156822,Human_miRNA_ID_3161621,Human_miRNA_ID_3161856,Human_miRNA_ID_3168172,Human_miRNA_ID_3168391,Human_miRNA_ID_3168610,Human_miRNA_ID_3168831,Human_miRNA_ID_3169045,Human_miRNA_ID_3180444,Human_miRNA_ID_3180662,Human_miRNA_ID_3195489,Human_miRNA_ID_3197921,Human_miRNA_ID_3198288,Human_miRNA_ID_3198673,Human_miRNA_ID_3198892,Human_miRNA_ID_3199162,Human_miRNA_ID_3199527,Human_miRNA_ID_3199861,Human_miRNA_ID_3200097,Human_miRNA_ID_3201025,Human_miRNA_ID_3215953 RMVar_hsa_circ_196399 15457 RMVar_ID_15457 Human_SNP_ID_670666958 A-to-I Human chr19 + 57304919 57304919 57304919 AAAATTAGCCAGACGTGGTGGCAGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGACAGGAGA AAAATTAGCCAGACGTGGTGGCAGGCGCCTGTGGTCCCAGCTACTCGGGAGGCTGAGACAGGAGA A G AC005261.1 Ensembl:ENSG00000268205 lincRNA exon GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1283665466 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196399 15458 RMVar_ID_15458 Human_SNP_ID_670666960 A-to-I Human chr19 + 57304929 57304929 57304929 AGACGTGGTGGCAGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGACAGGAGAATGGCATGAA AGACGTGGTGGCAGGCGCCTGTAGTCCCAGCTGCTCGGGAGGCTGAGACAGGAGAATGGCATGAA A G AC005261.1 Ensembl:ENSG00000268205 lincRNA exon GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1281472994 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196399 15459 RMVar_ID_15459 Human_SNP_ID_670666961 A-to-I Human chr19 + 57304929 57304929 57304929 AGACGTGGTGGCAGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGACAGGAGAATGGCATGAA AGACGTGGTGGCAGGCGCCTGTAGTCCCAGCTTCTCGGGAGGCTGAGACAGGAGAATGGCATGAA A T AC005261.1 Ensembl:ENSG00000268205 lincRNA exon GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1281472994 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196399 15460 RMVar_ID_15460 Human_SNP_ID_670666998 A-to-I Human chr19 + 57305022 57305021 57305023 AGATCACCCCACTGCACTCCAGCCTGGGCGACAGAGTGAAGGCTATGTCTCAAGAAAAAAAAAAA AGATCACCCCACTGCACTCCAGCCTGGGCGAC__AGTGAAGGCTATGTCTCAAGAAAAAAAAAAA CAG C AC005261.1 Ensembl:ENSG00000268205 lincRNA exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1392915093 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_6787626,Human_RBP_ID_25435462 Human_miRNA_ID_3201142 RMVar_hsa_circ_196399 15461 RMVar_ID_15461 Human_SNP_ID_670667000 A-to-I Human chr19 + 57305034 57305034 57305034 TGCACTCCAGCCTGGGCGACAGAGTGAAGGCTATGTCTCAAGAAAAAAAAAAAAAAACTTTTATA TGCACTCCAGCCTGGGCGACAGAGTGAAGGCTGTGTCTCAAGAAAAAAAAAAAAAAACTTTTATA A G AC005261.1 Ensembl:ENSG00000268205 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs927955738 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6787626,Human_RBP_ID_21891958 Human_miRNA_ID_3201142 RMVar_hsa_circ_196399 15462 RMVar_ID_15462 Human_SNP_ID_670667149 A-to-I Human chr19 + 57305556 57305556 57305556 TTTTTTTTTTTTTTGAGATGGGGTCTTGCTCTATCCCCCAGGCTGGAGTGCAGTTGTGCAGTCAT TTTTTTTTTTTTTTGAGATGGGGTCTTGCTCTGTCCCCCAGGCTGGAGTGCAGTTGTGCAGTCAT A G AC005261.1 Ensembl:ENSG00000268205 lincRNA exon GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1341444198 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_774030,Human_RBP_ID_912191,Human_RBP_ID_3588981,Human_RBP_ID_4549713,Human_RBP_ID_5088944,Human_RBP_ID_5193833,Human_RBP_ID_6787650,Human_RBP_ID_13518666 RMVar_hsa_circ_196399 15463 RMVar_ID_15463 Human_SNP_ID_670667171 A-to-I Human chr19 + 57305645 57305645 57305645 GGCCTAAGCAGTCCTCCTGCCTCAACCTCCCTAGTAGCTGAGACCACAGGCGCATGCCACCTGTG GGCCTAAGCAGTCCTCCTGCCTCAACCTCCCTGGTAGCTGAGACCACAGGCGCATGCCACCTGTG A G AC005261.1 Ensembl:ENSG00000268205 lincRNA exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1251229836 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8199782,Human_RBP_ID_13518675 RMVar_hsa_circ_196399 15464 RMVar_ID_15464 Human_SNP_ID_670667195 A-to-I Human chr19 + 57305754 57305754 57305754 GAACTCCTGGGCTCAAGTGATCCTCCTGCCTCAGCCTTCCAAAGTGTTGGATTACAGGCGTGAGC GAACTCCTGGGCTCAAGTGATCCTCCTGCCTCCGCCTTCCAAAGTGTTGGATTACAGGCGTGAGC A C AC005261.1 Ensembl:ENSG00000268205 lincRNA exon GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs531818192 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196399 15465 RMVar_ID_15465 Human_SNP_ID_670667600 A-to-I Human chr19 + 57307409 57307409 57307409 TGTATACAGGCCGGGTGCAGTGGCTCACTCCTATAATCCCAGCATTTTGGAAGTCCTATGCAGGA TGTATACAGGCCGGGTGCAGTGGCTCACTCCTGTAATCCCAGCATTTTGGAAGTCCTATGCAGGA A G AC005261.1 Ensembl:ENSG00000268205 lincRNA exon GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs11537833 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4549748,Human_RBP_ID_5088947,Human_RBP_ID_5261888,Human_RBP_ID_6787743,Human_RBP_ID_8199783,Human_RBP_ID_18515040 RMVar_hsa_circ_196399 15466 RMVar_ID_15466 Human_SNP_ID_670674488 A-to-I Human chr19 + 57330093 57330093 57330093 GTCCTGCAACGTTCTCCACTCTCGAGGTGCAGAAGCATACATCTTTATAAAAAATATGGAGGCTT GTCCTGCAACGTTCTCCACTCTCGAGGTGCAGGAGCATACATCTTTATAAAAAATATGGAGGCTT A G ZNF543 Ensembl:ENSG00000178229 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2361121 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17932032,Human_RBP_ID_26816351,Human_RBP_ID_27683479 15467 RMVar_ID_15467 Human_SNP_ID_670674489 A-to-I Human chr19 + 57330093 57330093 57330093 GTCCTGCAACGTTCTCCACTCTCGAGGTGCAGAAGCATACATCTTTATAAAAAATATGGAGGCTT GTCCTGCAACGTTCTCCACTCTCGAGGTGCAGTAGCATACATCTTTATAAAAAATATGGAGGCTT A T ZNF543 Ensembl:ENSG00000178229 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2361121 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17932032,Human_RBP_ID_26816351,Human_RBP_ID_27683479 15468 RMVar_ID_15468 Human_SNP_ID_670674895 A-to-I Human chr19 + 57331413 57331413 57331413 GCTCACTGCAGCCGCCTCCACCTTCCGGGTTCAAGTGATTTTCCTGCCTCAGCCTCCCAAGTAGC GCTCACTGCAGCCGCCTCCACCTTCCGGGTTCTAGTGATTTTCCTGCCTCAGCCTCCCAAGTAGC A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1043760827 Functional Loss SNV dbSNP153 33..33 33 - - - 15469 RMVar_ID_15469 Human_SNP_ID_670674929 A-to-I Human chr19 + 57331564 57331564 57331564 TTCATCTCTTAACCTTGTGATCTGCCTGGCTCAACCTTCCAAAGTGTTGGGATTACAGGCGTGGC TTCATCTCTTAACCTTGTGATCTGCCTGGCTCCACCTTCCAAAGTGTTGGGATTACAGGCGTGGC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335403690 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13518897 15470 RMVar_ID_15470 Human_SNP_ID_670675097 A-to-I Human chr19 + 57332176 57332176 57332176 AAACCTAGCCAGGCAAGGTTGCAGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGAAGA AAACCTAGCCAGGCAAGGTTGCAGGCGCCTGTGGTCCCAGCTACTCGGGAGGCTGAGGCAGAAGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973621036 Functional Loss SNV dbSNP153 33..33 33 - - - 15471 RMVar_ID_15471 Human_SNP_ID_670675100 A-to-I Human chr19 + 57332182 57332182 57332182 AGCCAGGCAAGGTTGCAGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGAAGAATTGTT AGCCAGGCAAGGTTGCAGGCGCCTGTAGTCCCGGCTACTCGGGAGGCTGAGGCAGAAGAATTGTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs889697817 Functional Loss SNV dbSNP153 33..33 33 - - - 15472 RMVar_ID_15472 Human_SNP_ID_670675306 A-to-I Human chr19 + 57332964 57332964 57332964 ATTACTAGCACACTCCACTATGCCCAGCTAATATTTGTGTATTTTGTAGAGATGAGGTTTCACCA ATTACTAGCACACTCCACTATGCCCAGCTAATTTTTGTGTATTTTGTAGAGATGAGGTTTCACCA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs977545465 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2571076,Human_RBP_ID_13518914,Human_RBP_ID_17932048 15473 RMVar_ID_15473 Human_SNP_ID_670675976 A-to-I Human chr19 + 57335524 57335524 57335524 AAAAATTAGCTGGCGTGGTGGCGGGCTCCTGTAATCCCAGGTACTCGGAAGGCTGAGGCAGAAGA AAAAATTAGCTGGCGTGGTGGCGGGCTCCTGTTATCCCAGGTACTCGGAAGGCTGAGGCAGAAGA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1386608794 Functional Loss SNV dbSNP153 33..33 33 - - - 15474 RMVar_ID_15474 Human_SNP_ID_670676004 A-to-I Human chr19 + 57335602 57335602 57335602 GGGAGGCGGAGGGTGCAGTGAGCTGAGATCGCACCACTGCACTCCAGCCTGGCGGCAGGGCAAGA GGGAGGCGGAGGGTGCAGTGAGCTGAGATCGCCCCACTGCACTCCAGCCTGGCGGCAGGGCAAGA A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1406897128 Functional Loss SNV dbSNP153 33..33 33 - - - 15475 RMVar_ID_15475 Human_SNP_ID_670676719 A-to-I Human chr19 + 57338516 57338516 57338516 GTCAGAGGCCAGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGCAGGGAGG GTCAGAGGCCAGGCACGGTGGCTCACGCCTGTGATCCCAGCACTTTGGGAGGCCGAGCAGGGAGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs967472173 Functional Loss SNV dbSNP153 33..33 33 - - - 15476 RMVar_ID_15476 Human_SNP_ID_670677201 A-to-I Human chr19 + 57340373 57340373 57340373 GAACCCTTGACCTCAATTGATCCACCCTCTTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG GAACCCTTGACCTCAATTGATCCACCCTCTTCTGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs897501272 Functional Loss SNV dbSNP153 33..33 33 - - - 15477 RMVar_ID_15477 Human_SNP_ID_670694725 A-to-I Human chr19 + 57407682 57407682 57407682 CAAATGATCCTTCCACCTCCACCTTTCAAAGTACTGGGATTACAGGCATGAGCCACTGTGCCCAG CAAATGATCCTTCCACCTCCACCTTTCAAAGTCCTGGGATTACAGGCATGAGCCACTGTGCCCAG A C AC003002.3,AC003002.2 Ensembl:ENSG00000269533,Ensembl:ENSG00000268533 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs558963640 Functional Loss SNV dbSNP153 33..33 33 - - - 15478 RMVar_ID_15478 Human_SNP_ID_670694726 A-to-I Human chr19 + 57407682 57407682 57407682 CAAATGATCCTTCCACCTCCACCTTTCAAAGTACTGGGATTACAGGCATGAGCCACTGTGCCCAG CAAATGATCCTTCCACCTCCACCTTTCAAAGTGCTGGGATTACAGGCATGAGCCACTGTGCCCAG A G AC003002.3,AC003002.2 Ensembl:ENSG00000269533,Ensembl:ENSG00000268533 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs558963640 Functional Loss SNV dbSNP153 33..33 33 - - - 15479 RMVar_ID_15479 Human_SNP_ID_670696053 A-to-I Human chr19 + 57412620 57412620 57412620 GTGCCCGCCACCACGCCAGGCTAATTTTTTGCATTTTTAGTAGAGACGGGGTTTCACCGTGTTAG GTGCCCGCCACCACGCCAGGCTAATTTTTTGCGTTTTTAGTAGAGACGGGGTTTCACCGTGTTAG A G ZNF17,AC003002.3,AC003002.2 Ensembl:ENSG00000186272,Ensembl:ENSG00000269533,Ensembl:ENSG00000268533 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs529982015 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13519326 15480 RMVar_ID_15480 Human_SNP_ID_670699691 A-to-I Human chr19 + 57426195 57426195 57426195 TGGGCCTCACAAAGTGCTGTGATTACAGGCTTAAGCCACCACCCCTGGCCAATTTTTTCATAATA TGGGCCTCACAAAGTGCTGTGATTACAGGCTTCAGCCACCACCCCTGGCCAATTTTTTCATAATA A C AC003002.2 Ensembl:ENSG00000268533 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886646217 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6806475 RMVar_hsa_circ_196413,RMVar_hsa_circ_196412 15481 RMVar_ID_15481 Human_SNP_ID_670704753 A-to-I Human chr19 + 57445814 57445814 57445814 AGCTGGGCATGGTGGCAGGTGCCTGTAATCCCAGCTATTCAGGGGACTGAGGCAGGGAGCATCAC AGCTGGGCATGGTGGCAGGTGCCTGTAATCCCGGCTATTCAGGGGACTGAGGCAGGGAGCATCAC A G ZNF749 Ensembl:ENSG00000186230 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1311437407 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80511,RMVar_hsa_circ_104082,RMVar_hsa_circ_196415,RMVar_hsa_circ_196416 15482 RMVar_ID_15482 Human_SNP_ID_670705627 A-to-I Human chr19 + 57448632 57448632 57448632 TATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGGTCTTGATCTTCCTGACTTTGTG TATTTTTAGTAGAGACGGGGTTTCACCGTGTTCGCCAGGATGGTCTTGATCTTCCTGACTTTGTG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs371387049 Functional Loss SNV dbSNP153 33..33 33 - - - 15483 RMVar_ID_15483 Human_SNP_ID_670705628 A-to-I Human chr19 + 57448632 57448632 57448632 TATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGGTCTTGATCTTCCTGACTTTGTG TATTTTTAGTAGAGACGGGGTTTCACCGTGTTGGCCAGGATGGTCTTGATCTTCCTGACTTTGTG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs371387049 Functional Loss SNV dbSNP153 33..33 33 - - - 15484 RMVar_ID_15484 Human_SNP_ID_670705629 A-to-I Human chr19 + 57448632 57448632 57448632 TATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGGTCTTGATCTTCCTGACTTTGTG TATTTTTAGTAGAGACGGGGTTTCACCGTGTTTGCCAGGATGGTCTTGATCTTCCTGACTTTGTG A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs371387049 Functional Loss SNV dbSNP153 33..33 33 - - - 15485 RMVar_ID_15485 Human_SNP_ID_670705688 A-to-I Human chr19 + 57448678 57448678 57448678 TGATCTTCCTGACTTTGTGATCCATCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG TGATCTTCCTGACTTTGTGATCCATCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs531513371 Functional Loss SNV dbSNP153 33..33 33 - - - 15486 RMVar_ID_15486 Human_SNP_ID_670707653 A-to-I Human chr19 - 57455747 57455747 57455747 CTGGGCCAGTGGCTCCATGGTCTTCTTCCTCTACAGACACAAGCAGCAAGTCCAACACAATCACA CTGGGCCAGTGGCTCCATGGTCTTCTTCCTCTGCAGACACAAGCAGCAAGTCCAACACAATCACA T C VN1R1,AC004076.1 Ensembl:ENSG00000178201,Ensembl:ENSG00000268163 Protein coding,Protein coding CDS,intron GSE107867 ASD brains,frontal_cortex;ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs560731515 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22666920 Human_Splice_Rec_2050167 RMVar_hsa_circ_196418,RMVar_hsa_circ_196420,RMVar_hsa_circ_273856,RMVar_hsa_circ_196419,RMVar_hsa_circ_196417 15487 RMVar_ID_15487 Human_SNP_ID_670709665 A-to-I Human chr19 - 57463102 57463102 57463102 GCCACCACGCCCGGATAATTTTTTGTATTTTTAGTAGAGACGGAGTTTCTCCGTGTTGGTCAAGC GCCACCACGCCCGGATAATTTTTTGTATTTTTGGTAGAGACGGAGTTTCTCCGTGTTGGTCAAGC T C AC004076.1 Ensembl:ENSG00000268163 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs577069930 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196418,RMVar_hsa_circ_196417 15488 RMVar_ID_15488 Human_SNP_ID_670747615 A-to-I Human chr19 + 57607408 57607408 57607408 TGCTCGTCACCCAGGCTGGAGTGCAATTGTGCAATCTCAGCTCACTGCAACCTCCGCCTCCTGGG TGCTCGTCACCCAGGCTGGAGTGCAATTGTGCGATCTCAGCTCACTGCAACCTCCGCCTCCTGGG A G ZNF530 Ensembl:ENSG00000183647 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1007747284 Functional Loss SNV dbSNP153 33..33 33 - - - 15489 RMVar_ID_15489 Human_SNP_ID_670747617 A-to-I Human chr19 + 57607419 57607419 57607419 CAGGCTGGAGTGCAATTGTGCAATCTCAGCTCACTGCAACCTCCGCCTCCTGGGATCAAGTGATT CAGGCTGGAGTGCAATTGTGCAATCTCAGCTCGCTGCAACCTCCGCCTCCTGGGATCAAGTGATT A G ZNF530 Ensembl:ENSG00000183647 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1259089682 Functional Loss SNV dbSNP153 33..33 33 - - - 15490 RMVar_ID_15490 Human_SNP_ID_670748049 A-to-I Human chr19 + 57609246 57609246 57609246 CCAGCTGCTCTGAAGGCTGACGCACCAAGAATAGCTTGAACCCGGAAGTGGAGGTTGCAGTGAGC CCAGCTGCTCTGAAGGCTGACGCACCAAGAATGGCTTGAACCCGGAAGTGGAGGTTGCAGTGAGC A G ZNF530 Ensembl:ENSG00000183647 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335350794 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13520698,Human_RBP_ID_23310243 15491 RMVar_ID_15491 Human_SNP_ID_670767582 A-to-I Human chr19 + 57685341 57685341 57685341 GGAGCTCCTTGATGAGTCTCAGAGGTTCCTGTACTGCGATGTGATGCTGGAGAACTTTGCACATG GGAGCTCCTTGATGAGTCTCAGAGGTTCCTGTGCTGCGATGTGATGCTGGAGAACTTTGCACATG A G AC003006.1,ZNF551 Ensembl:ENSG00000269026,Ensembl:ENSG00000204519 Protein coding,Protein coding intron,CDS GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1368134462 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1572967,Human_RBP_ID_1892618,Human_RBP_ID_18740628,Human_RBP_ID_23809363 Human_Splice_Rec_2050590,Human_Splice_Rec_2050591,Human_Splice_Rec_2050594,Human_Splice_Rec_2050595,Human_Splice_Rec_2050600,Human_Splice_Rec_2050601 Human_miRNA_ID_1541688,Human_miRNA_ID_1595130,Human_miRNA_ID_2442451 RMVar_hsa_circ_196433,RMVar_hsa_circ_104849 15492 RMVar_ID_15492 Human_SNP_ID_670768556 A-to-I Human chr19 - 57688042 57688034 57688043 GAGCTCTGGCTAAAGGATTTCCCACATTCACTACATTCATAAGGCCTTTCTCCAGTGTGAACTCT GAGCTCTGGCTAAAGGATTTCCCACATTCAC_________AAGGCCTTTCTCCAGTGTGAACTCT TATGAATGTA T - - Other Unknown GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1206720345 Functional Loss DEL dbSNP153 32..40 33 - - - 15493 RMVar_ID_15493 Human_SNP_ID_670768560 A-to-I Human chr19 - 57688042 57688042 57688042 GAGCTCTGGCTAAAGGATTTCCCACATTCACTACATTCATAAGGCCTTTCTCCAGTGTGAACTCT GAGCTCTGGCTAAAGGATTTCCCACATTCACTGCATTCATAAGGCCTTTCTCCAGTGTGAACTCT T C - - Other Unknown GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) - Functional Loss SNV HGVD 33..33 33 - - - 15494 RMVar_ID_15494 Human_SNP_ID_670768821 A-to-I Human chr19 - 57688912 57688902 57688912 CACCCCTTCATGCTGACATCACTATTCTGCTTACAAGTCATTCTATGCAATGAATAGAACACCCA CACCCCTTCATGCTGACATCACTATTCTGCTT__________CTATGCAATGAATAGAACACCCA GAATGACTTGT G - - Other Unknown GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1338867200 Functional Loss DEL dbSNP153 33..42 33 - - - 15495 RMVar_ID_15495 Human_SNP_ID_670771487 A-to-I Human chr19 - 57698968 57698968 57698968 CAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCTGGGCATAGTGGCATGCACCT CAACATGGTGAAACCCCGTCTCTACTAAAAATGCAAAAATTAGCTGGGCATAGTGGCATGCACCT T C ZNF154 Ensembl:ENSG00000179909 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1568460116 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196437 15496 RMVar_ID_15496 Human_SNP_ID_670778175 A-to-I Human chr19 - 57725381 57725381 57725381 CGGCTCACCGCAACCTCTGCCTTCTGGGTTCAAGCAATTCTCTTGTCTGCCTCCTGAGTAGCTGG CGGCTCACCGCAACCTCTGCCTTCTGGGTTCAGGCAATTCTCTTGTCTGCCTCCTGAGTAGCTGG T C ZNF671 Ensembl:ENSG00000083814 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1307495415 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1296016 RMVar_hsa_circ_196443 15497 RMVar_ID_15497 Human_SNP_ID_670784301 A-to-I Human chr19 + 57749172 57749172 57749172 TTTTGTATTTTTAGTAGAGATGTGATTTCACCATATTGGCCAGGCTGGTCTCGAACTCCTGACCT TTTTGTATTTTTAGTAGAGATGTGATTTCACCGTATTGGCCAGGCTGGTCTCGAACTCCTGACCT A G ZNF776,AC003006.1 Ensembl:ENSG00000152443,Ensembl:ENSG00000269026 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1040380556 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2050654 RMVar_hsa_circ_196433,RMVar_hsa_circ_104849,RMVar_hsa_circ_100899,RMVar_hsa_circ_196444 15498 RMVar_ID_15498 Human_SNP_ID_670784554 A-to-I Human chr19 + 57750364 57750364 57750364 TAAGGCCAGAGAATTACTCGAGCCCAGTAGACAGAGGTTGCAGAGAGCTGAGATTATGTCATTGC TAAGGCCAGAGAATTACTCGAGCCCAGTAGACGGAGGTTGCAGAGAGCTGAGATTATGTCATTGC A G ZNF776,AC003006.1 Ensembl:ENSG00000152443,Ensembl:ENSG00000269026 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs749862368 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196433,RMVar_hsa_circ_104849,RMVar_hsa_circ_100899,RMVar_hsa_circ_196444 15499 RMVar_ID_15499 Human_SNP_ID_670789908 A-to-I Human chr19 + 57770325 57770325 57770325 ATTACAGGCATGCGCCACCACGGGGTTTCACCATGTTGGCTAGGCTGGCCTCGAACTCCTGACCT ATTACAGGCATGCGCCACCACGGGGTTTCACCCTGTTGGCTAGGCTGGCCTCGAACTCCTGACCT A C ZNF586 Ensembl:ENSG00000083828 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs898707100 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6789586,Human_RBP_ID_24376234 RMVar_hsa_circ_110349,RMVar_hsa_circ_196445,RMVar_hsa_circ_196447,RMVar_hsa_circ_103002,RMVar_hsa_circ_119754,RMVar_hsa_circ_196448 15500 RMVar_ID_15500 Human_SNP_ID_670790062 A-to-I Human chr19 + 57770951 57770951 57770951 CGGCGCAGCACGGCCTCGACCTCTCCGGGCTCAGGAGAGCCTCTCATCTCAGTCTCCCGAGTAAC CGGCGCAGCACGGCCTCGACCTCTCCGGGCTCGGGAGAGCCTCTCATCTCAGTCTCCCGAGTAAC A G ZNF586 Ensembl:ENSG00000083828 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1214804492 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110349,RMVar_hsa_circ_196445,RMVar_hsa_circ_196447,RMVar_hsa_circ_103002,RMVar_hsa_circ_119754,RMVar_hsa_circ_196448 15501 RMVar_ID_15501 Human_SNP_ID_670790845 A-to-I Human chr19 + 57774035 57774035 57774035 GCCGGGGGTTCGAGATCAGCGTCGCCAACATGATGAAAGCCCATCTCTACTAAAAATACAAAAAA GCCGGGGGTTCGAGATCAGCGTCGCCAACATGGTGAAAGCCCATCTCTACTAAAAATACAAAAAA A G ZNF586 Ensembl:ENSG00000083828 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs901816224 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110349,RMVar_hsa_circ_196445,RMVar_hsa_circ_196447,RMVar_hsa_circ_103002,RMVar_hsa_circ_119754,RMVar_hsa_circ_196448 15502 RMVar_ID_15502 Human_SNP_ID_670791160 A-to-I Human chr19 + 57775053 57775053 57775053 ACGGAGTCTCGCTCTGTCGCCCAGGCTGGAGTACAGTGGCAGATCTCATCTCACTGCAAGCTCCG ACGGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCAGATCTCATCTCACTGCAAGCTCCG A G ZNF586 Ensembl:ENSG00000083828 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs974718228 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110349,RMVar_hsa_circ_196445,RMVar_hsa_circ_196447,RMVar_hsa_circ_103002,RMVar_hsa_circ_119754,RMVar_hsa_circ_196448 15503 RMVar_ID_15503 Human_SNP_ID_670793110 A-to-I Human chr19 + 57782245 57782244 57782246 AATTTTCTCTTTTATTTTTTATTCTTTGAGACAGAGTTTCACTCTTGTTGCCCAGGCTGGGGTGC AATTTTCTCTTTTATTTTTTATTCTTTGAGAC__AGTTTCACTCTTGTTGCCCAGGCTGGGGTGC CAG C ZNF586 Ensembl:ENSG00000083828 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1205198837 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_110349,RMVar_hsa_circ_196445,RMVar_hsa_circ_103002,RMVar_hsa_circ_196448,RMVar_hsa_circ_123505,RMVar_hsa_circ_196452 15504 RMVar_ID_15504 Human_SNP_ID_670793113 A-to-I Human chr19 + 57782245 57782245 57782245 AATTTTCTCTTTTATTTTTTATTCTTTGAGACAGAGTTTCACTCTTGTTGCCCAGGCTGGGGTGC AATTTTCTCTTTTATTTTTTATTCTTTGAGACGGAGTTTCACTCTTGTTGCCCAGGCTGGGGTGC A G ZNF586 Ensembl:ENSG00000083828 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1481339566 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110349,RMVar_hsa_circ_196445,RMVar_hsa_circ_103002,RMVar_hsa_circ_196448,RMVar_hsa_circ_123505,RMVar_hsa_circ_196452 15505 RMVar_ID_15505 Human_SNP_ID_670793463 A-to-I Human chr19 + 57783536 57783536 57783536 GTTGTTGGCCGGGCATGGTGGTTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGACAG GTTGTTGGCCGGGCATGGTGGTTCACACCTGTGATCCCAGCACTTTGGGAGGCTGAGGCAGACAG A G ZNF586 Ensembl:ENSG00000083828 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1158020459 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110349,RMVar_hsa_circ_196445,RMVar_hsa_circ_103002,RMVar_hsa_circ_196448,RMVar_hsa_circ_123505,RMVar_hsa_circ_196452 15506 RMVar_ID_15506 Human_SNP_ID_670795209 A-to-I Human chr19 - 57789459 57789454 57789459 GCAATTACAGCTCACTGCAGCCTGAACTTTCCAGGTTTCAGGGATCCTCCTACCTCAGCCTCCCG GCAATTACAGCTCACTGCAGCCTGAACTTTCC_____TCAGGGATCCTCCTACCTCAGCCTCCCG AAACCT A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1479403933 Functional Loss DEL dbSNP153 33..37 33 - - - 15507 RMVar_ID_15507 Human_SNP_ID_670795316 A-to-I Human chr19 - 57789860 57789860 57789860 TGCCACCAACACCTAACTCCCCCACACCATAGACCTCTCTCTGGCCTTGCCAGAAGTTAAAGTAT TGCCACCAACACCTAACTCCCCCACACCATAGGCCTCTCTCTGGCCTTGCCAGAAGTTAAAGTAT T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6510097 Functional Loss SNV dbSNP153 33..33 33 - - - 15508 RMVar_ID_15508 Human_SNP_ID_670795467 A-to-I Human chr19 + 57790390 57790390 57790390 CATGATGTGATGCTGGAGACCTTGACACTTATATCCTCCCTGGGTAAGGTACTCATACTTAACTG CATGATGTGATGCTGGAGACCTTGACACTTATGTCCTCCCTGGGTAAGGTACTCATACTTAACTG A G ZNF586 Ensembl:ENSG00000083828 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1568486606 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8495235 Human_Splice_Rec_2050675,Human_Splice_Rec_2050679,Human_Splice_Rec_2050683 RMVar_hsa_circ_110349,RMVar_hsa_circ_196445,RMVar_hsa_circ_103002,RMVar_hsa_circ_196448,RMVar_hsa_circ_123505,RMVar_hsa_circ_196452,RMVar_hsa_circ_196453,RMVar_hsa_circ_121905,RMVar_hsa_circ_333835 15509 RMVar_ID_15509 Human_SNP_ID_670795556 A-to-I Human chr19 - 57790646 57790646 57790646 AAAGGCAGAAGACAACCAAGGTGGGATGCATTAGGGTGACTTTAAGACTCCTGACCCTAACTCTT AAAGGCAGAAGACAACCAAGGTGGGATGCATTGGGGTGACTTTAAGACTCCTGACCCTAACTCTT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs892922495 Functional Loss SNV dbSNP153 33..33 33 - - - 15510 RMVar_ID_15510 Human_SNP_ID_670795917 A-to-I Human chr19 + 57791826 57791826 57791826 TGCAGATGGGCATGGTGGCTCATGCCTGTGATACCAGCACTTTGGGAGGCCGAGGCAGAAGGGTC TGCAGATGGGCATGGTGGCTCATGCCTGTGATCCCAGCACTTTGGGAGGCCGAGGCAGAAGGGTC A C ZNF586 Ensembl:ENSG00000083828 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1399614639 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103002,RMVar_hsa_circ_196448,RMVar_hsa_circ_196453,RMVar_hsa_circ_121905 15511 RMVar_ID_15511 Human_SNP_ID_670795934 A-to-I Human chr19 + 57791892 57791892 57791892 GTTGAGGTCAGGAGTTCCAGACCAGCCTGGCCAACATGCTGAAACCCCATCTCTACTAAAAATAC GTTGAGGTCAGGAGTTCCAGACCAGCCTGGCCCACATGCTGAAACCCCATCTCTACTAAAAATAC A C ZNF586 Ensembl:ENSG00000083828 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1476044914 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103002,RMVar_hsa_circ_196448,RMVar_hsa_circ_196453,RMVar_hsa_circ_121905 15512 RMVar_ID_15512 Human_SNP_ID_670798281 A-to-I Human chr19 + 57801397 57801397 57801397 TCACCCAGGCTACAGTGCAGTGGCGCGATGTCAGCTCACTGCAACCTCCGCCTCCCGGGTTCAAG TCACCCAGGCTACAGTGCAGTGGCGCGATGTCGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAG A G ZNF586 Ensembl:ENSG00000083828 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1339785257 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196453,RMVar_hsa_circ_121905 15513 RMVar_ID_15513 Human_SNP_ID_670798337 A-to-I Human chr19 + 57801602 57801602 57801602 CACCAGCCTCGGCCTCCCAAAGTGCTGGGATTACAGTCATGAGCCACCACGCCCAGCCTACTTAT CACCAGCCTCGGCCTCCCAAAGTGCTGGGATTCCAGTCATGAGCCACCACGCCCAGCCTACTTAT A C ZNF586 Ensembl:ENSG00000083828 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913698526 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196453,RMVar_hsa_circ_121905 15514 RMVar_ID_15514 Human_SNP_ID_670799299 A-to-I Human chr19 + 57804990 57804990 57804990 GTATTTTTCCTAGAGACGGGGTTTCATGTGTTAGCCACATGGTCTTGATATCCTGACCTCGTTAC GTATTTTTCCTAGAGACGGGGTTTCATGTGTTGGCCACATGGTCTTGATATCCTGACCTCGTTAC A G ZNF586 Ensembl:ENSG00000083828 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs767637458 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196453,RMVar_hsa_circ_121905 15515 RMVar_ID_15515 Human_SNP_ID_670799610 A-to-I Human chr19 - 57806077 57806077 57806077 TGAGCTGAGATCACACCACTGCACTCCAGCCTAGGCGACAGTTAGACGCTGTCTCAAAAAAAATA TGAGCTGAGATCACACCACTGCACTCCAGCCTGGGCGACAGTTAGACGCTGTCTCAAAAAAAATA T C ZNF552 Ensembl:ENSG00000178935 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs939897794 Functional Loss SNV dbSNP153 33..33 33 - - - 15516 RMVar_ID_15516 Human_SNP_ID_670799764 A-to-I Human chr19 - 57806674 57806674 57806674 GACCTTGTGATCCGCCCATCTCGGCCTCCCATAGTGCTAGCATTACAGGCATGAGCCATCGCGTG GACCTTGTGATCCGCCCATCTCGGCCTCCCATCGTGCTAGCATTACAGGCATGAGCCATCGCGTG T G ZNF552 Ensembl:ENSG00000178935 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1226242079 Functional Loss SNV dbSNP153 33..33 33 - - - 15517 RMVar_ID_15517 Human_SNP_ID_670800688 A-to-I Human chr19 - 57809884 57809883 57809885 GATCTCCTGGGCCTGAGTGATCCCTTTGCCTTAGCCTCCCAAAGTGCTGGGATTGTAGGCATGAG GATCTCCTGGGCCTGAGTGATCCCTTTGCCT__GCCTCCCAAAGTGCTGGGATTGTAGGCATGAG CTA C ZNF552 Ensembl:ENSG00000178935 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1158743884 Functional Loss DEL dbSNP153 32..33 33 - - - 15518 RMVar_ID_15518 Human_SNP_ID_670805545 A-to-I Human chr19 + 57827087 57827087 57827087 TAGAGACGGGGTTTCACCATGTTGGCCAGGATAGTCTGTAGCTCTTAACCTCGTGATCCCCTCAC TAGAGACGGGGTTTCACCATGTTGGCCAGGATCGTCTGTAGCTCTTAACCTCGTGATCCCCTCAC A C AC010522.1,ZNF587B Ensembl:ENSG00000268750,Ensembl:ENSG00000269343 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs541133194 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23310002 RMVar_hsa_circ_196453,RMVar_hsa_circ_121905 15519 RMVar_ID_15519 Human_SNP_ID_670808205 A-to-I Human chr19 + 57836706 57836706 57836706 ATATATCTGAACGGGTGCAGTGCCTCATGCCTATAATCCTAGCACTTTAGGAGGCCGAGATGGGT ATATATCTGAACGGGTGCAGTGCCTCATGCCTGTAATCCTAGCACTTTAGGAGGCCGAGATGGGT A G AC010522.1,ZNF587B Ensembl:ENSG00000268750,Ensembl:ENSG00000269343 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1279423513 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196453,RMVar_hsa_circ_121905 15520 RMVar_ID_15520 Human_SNP_ID_670808567 A-to-I Human chr19 + 57837845 57837845 57837845 GACCTCAGGCGATCCACCCGGCTCAGCCTCCTAAAGCACTGGTACTACAGGTGCGAGCCACCACG GACCTCAGGCGATCCACCCGGCTCAGCCTCCTCAAGCACTGGTACTACAGGTGCGAGCCACCACG A C AC010522.1,ZNF587B Ensembl:ENSG00000268750,Ensembl:ENSG00000269343 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs944690401 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196453,RMVar_hsa_circ_121905 15521 RMVar_ID_15521 Human_SNP_ID_670808732 A-to-I Human chr19 + 57838399 57838399 57838399 CCGAGGCAGATGGATCATGAGGTTAAGAGATCAAGACCATCCTGGCCAACATGATGAAACCCCGT CCGAGGCAGATGGATCATGAGGTTAAGAGATCGAGACCATCCTGGCCAACATGATGAAACCCCGT A G AC010522.1,ZNF587B Ensembl:ENSG00000268750,Ensembl:ENSG00000269343 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs938257870 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196453,RMVar_hsa_circ_121905 15522 RMVar_ID_15522 Human_SNP_ID_670808748 A-to-I Human chr19 + 57838460 57838460 57838460 CCGTCTCTACTAAAAATATAAAAATTAGCCAGATGTGGTGGCGGGTGCCTGTAGCCCCAGCTACT CCGTCTCTACTAAAAATATAAAAATTAGCCAGTTGTGGTGGCGGGTGCCTGTAGCCCCAGCTACT A T AC010522.1,ZNF587B Ensembl:ENSG00000268750,Ensembl:ENSG00000269343 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs936319904 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196453,RMVar_hsa_circ_121905 15523 RMVar_ID_15523 Human_SNP_ID_670808766 A-to-I Human chr19 + 57838533 57838533 57838533 TGAGGCAGAAGAATTGCTGGAACCCAGGAGGCAGAGGTTGCAGTGAGCCGAGATTGTGCCACTGC TGAGGCAGAAGAATTGCTGGAACCCAGGAGGCCGAGGTTGCAGTGAGCCGAGATTGTGCCACTGC A C AC010522.1,ZNF587B Ensembl:ENSG00000268750,Ensembl:ENSG00000269343 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs985167101 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196453,RMVar_hsa_circ_121905 15524 RMVar_ID_15524 Human_SNP_ID_670810507 A-to-I Human chr19 + 57843190 57843190 57843190 CTATTTTCTCATATTAGTAGATATAGGGTTTTACCATGTTTCCAGGCTGGTATCGAACTCCTGAG CTATTTTCTCATATTAGTAGATATAGGGTTTTGCCATGTTTCCAGGCTGGTATCGAACTCCTGAG A G AC010522.1,ZNF587B Ensembl:ENSG00000268750,Ensembl:ENSG00000269343 Protein coding,Protein coding intron,3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229,31158229 RNA-Seq:(High) rs928467440 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13522949 Human_miRNA_ID_2732288 RMVar_hsa_circ_196453,RMVar_hsa_circ_121905,RMVar_hsa_circ_112355,RMVar_hsa_circ_115228,RMVar_hsa_circ_196457,RMVar_hsa_circ_196458 15525 RMVar_ID_15525 Human_SNP_ID_670810821 A-to-I Human chr19 + 57843701 57843701 57843701 CTGGTTCATTGCAACCTCTGCCTCCTGAGTTCAAGCAATTCTCCTTTCTCAGCCTCCTGAGTAGC CTGGTTCATTGCAACCTCTGCCTCCTGAGTTCCAGCAATTCTCCTTTCTCAGCCTCCTGAGTAGC A C AC010522.1,ZNF587B Ensembl:ENSG00000268750,Ensembl:ENSG00000269343 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1220792664 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196453,RMVar_hsa_circ_121905,RMVar_hsa_circ_112355,RMVar_hsa_circ_115228,RMVar_hsa_circ_196457,RMVar_hsa_circ_196458 15526 RMVar_ID_15526 Human_SNP_ID_670810822 A-to-I Human chr19 + 57843701 57843701 57843701 CTGGTTCATTGCAACCTCTGCCTCCTGAGTTCAAGCAATTCTCCTTTCTCAGCCTCCTGAGTAGC CTGGTTCATTGCAACCTCTGCCTCCTGAGTTCTAGCAATTCTCCTTTCTCAGCCTCCTGAGTAGC A T AC010522.1,ZNF587B Ensembl:ENSG00000268750,Ensembl:ENSG00000269343 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1220792664 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196453,RMVar_hsa_circ_121905,RMVar_hsa_circ_112355,RMVar_hsa_circ_115228,RMVar_hsa_circ_196457,RMVar_hsa_circ_196458 15527 RMVar_ID_15527 Human_SNP_ID_670810847 A-to-I Human chr19 + 57843763 57843763 57843763 AGCTGGGATTACAGGTGCCTGCCACCACACCCAGGTAATTTTTGTACTTTTAGTAGAGATGGGGT AGCTGGGATTACAGGTGCCTGCCACCACACCCGGGTAATTTTTGTACTTTTAGTAGAGATGGGGT A G AC010522.1,ZNF587B Ensembl:ENSG00000268750,Ensembl:ENSG00000269343 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1568502012 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196453,RMVar_hsa_circ_121905,RMVar_hsa_circ_112355,RMVar_hsa_circ_115228,RMVar_hsa_circ_196457,RMVar_hsa_circ_196458 15528 RMVar_ID_15528 Human_SNP_ID_670810854 A-to-I Human chr19 + 57843802 57843802 57843802 TTTTGTACTTTTAGTAGAGATGGGGTTTCACTATGTTGGTCAAACTGATCTTGAACTCCTAACCT TTTTGTACTTTTAGTAGAGATGGGGTTTCACTGTGTTGGTCAAACTGATCTTGAACTCCTAACCT A G AC010522.1,ZNF587B Ensembl:ENSG00000268750,Ensembl:ENSG00000269343 Protein coding,Protein coding intron,intron GSE38233;GSE100210;GSE99789 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 24183664,29129909,29796672 RNA-Seq:(High) rs1482052441 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13522986 RMVar_hsa_circ_196453,RMVar_hsa_circ_121905,RMVar_hsa_circ_112355,RMVar_hsa_circ_115228,RMVar_hsa_circ_196457,RMVar_hsa_circ_196458 15529 RMVar_ID_15529 Human_SNP_ID_670810990 A-to-I Human chr19 + 57844321 57844321 57844321 AGGAAGGAGTTCAAGACCAGCCTGGGCAATATAGTGAAATCCTGTCTCTTCTAAAAATATAAAAA AGGAAGGAGTTCAAGACCAGCCTGGGCAATATGGTGAAATCCTGTCTCTTCTAAAAATATAAAAA A G AC010522.1,ZNF587B Ensembl:ENSG00000268750,Ensembl:ENSG00000269343 Protein coding,Protein coding intron,CDS GSE56152;GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 embryonic stem cells,wild type;HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 25708366,29129909,31158229 RNA-Seq:(High) rs1352494613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2378752,Human_miRNA_ID_2378753,Human_miRNA_ID_3093821,Human_miRNA_ID_3093822 RMVar_hsa_circ_196453,RMVar_hsa_circ_121905,RMVar_hsa_circ_112355,RMVar_hsa_circ_115228,RMVar_hsa_circ_196457,RMVar_hsa_circ_121548,RMVar_hsa_circ_196458,RMVar_hsa_circ_196459 15530 RMVar_ID_15530 Human_SNP_ID_670810999 A-to-I Human chr19 + 57844341 57844341 57844341 CCTGGGCAATATAGTGAAATCCTGTCTCTTCTAAAAATATAAAAATTAGCCGGGCATGGTGGCGC CCTGGGCAATATAGTGAAATCCTGTCTCTTCTGAAAATATAAAAATTAGCCGGGCATGGTGGCGC A G AC010522.1,ZNF587B Ensembl:ENSG00000268750,Ensembl:ENSG00000269343 Protein coding,Protein coding intron,stop codon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1198305490 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196453,RMVar_hsa_circ_121905,RMVar_hsa_circ_112355,RMVar_hsa_circ_115228,RMVar_hsa_circ_196457,RMVar_hsa_circ_121548,RMVar_hsa_circ_196458,RMVar_hsa_circ_196459 15531 RMVar_ID_15531 Human_SNP_ID_670811001 A-to-I Human chr19 + 57844344 57844344 57844344 GGGCAATATAGTGAAATCCTGTCTCTTCTAAAAATATAAAAATTAGCCGGGCATGGTGGCGCACC GGGCAATATAGTGAAATCCTGTCTCTTCTAAAGATATAAAAATTAGCCGGGCATGGTGGCGCACC A G AC010522.1,ZNF587B Ensembl:ENSG00000268750,Ensembl:ENSG00000269343 Protein coding,Protein coding intron,3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs775177667 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196453,RMVar_hsa_circ_121905,RMVar_hsa_circ_112355,RMVar_hsa_circ_115228,RMVar_hsa_circ_196457,RMVar_hsa_circ_121548,RMVar_hsa_circ_196458,RMVar_hsa_circ_196459 15532 RMVar_ID_15532 Human_SNP_ID_670811002 A-to-I Human chr19 + 57844344 57844344 57844344 GGGCAATATAGTGAAATCCTGTCTCTTCTAAAAATATAAAAATTAGCCGGGCATGGTGGCGCACC GGGCAATATAGTGAAATCCTGTCTCTTCTAAATATATAAAAATTAGCCGGGCATGGTGGCGCACC A T AC010522.1,ZNF587B Ensembl:ENSG00000268750,Ensembl:ENSG00000269343 Protein coding,Protein coding intron,3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs775177667 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196453,RMVar_hsa_circ_121905,RMVar_hsa_circ_112355,RMVar_hsa_circ_115228,RMVar_hsa_circ_196457,RMVar_hsa_circ_121548,RMVar_hsa_circ_196458,RMVar_hsa_circ_196459 15533 RMVar_ID_15533 Human_SNP_ID_670811010 A-to-I Human chr19 + 57844356 57844356 57844356 GAAATCCTGTCTCTTCTAAAAATATAAAAATTAGCCGGGCATGGTGGCGCACCTGTAGCCGCAGC GAAATCCTGTCTCTTCTAAAAATATAAAAATTTGCCGGGCATGGTGGCGCACCTGTAGCCGCAGC A T AC010522.1,ZNF587B Ensembl:ENSG00000268750,Ensembl:ENSG00000269343 Protein coding,Protein coding intron,3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1431821249 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13523021,Human_RBP_ID_23310003 RMVar_hsa_circ_196453,RMVar_hsa_circ_121905,RMVar_hsa_circ_112355,RMVar_hsa_circ_115228,RMVar_hsa_circ_196457,RMVar_hsa_circ_121548,RMVar_hsa_circ_196458,RMVar_hsa_circ_196459 15534 RMVar_ID_15534 Human_SNP_ID_670811029 A-to-I Human chr19 + 57844421 57844420 57844421 TACTCAGGAGGCTGAGGCAGGAAAATTGCTTGAACCCCGGGAGGTAGAGGTTGCAGTGAGCTGAG TACTCAGGAGGCTGAGGCAGGAAAATTGCTTG_ACCCCGGGAGGTAGAGGTTGCAGTGAGCTGAG GA G AC010522.1,ZNF587B Ensembl:ENSG00000268750,Ensembl:ENSG00000269343 Protein coding,Protein coding intron,3'UTR GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1224128312 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_196453,RMVar_hsa_circ_121905,RMVar_hsa_circ_112355,RMVar_hsa_circ_115228,RMVar_hsa_circ_196457,RMVar_hsa_circ_121548,RMVar_hsa_circ_196458,RMVar_hsa_circ_196459 15535 RMVar_ID_15535 Human_SNP_ID_670811192 A-to-I Human chr19 + 57845025 57845025 57845025 TTGAGACACAGTCTCACTCTGTCACCCAGGCTAGAGTGCTGTTGCACCATCTCGGCTCACTGCAA TTGAGACACAGTCTCACTCTGTCACCCAGGCTGGAGTGCTGTTGCACCATCTCGGCTCACTGCAA A G AC010522.1,ZNF587B Ensembl:ENSG00000268750,Ensembl:ENSG00000269343 Protein coding,Protein coding intron,3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1337489133 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6790148,Human_RBP_ID_13523067 Human_miRNA_ID_1968891,Human_miRNA_ID_1968892 RMVar_hsa_circ_196453,RMVar_hsa_circ_121905,RMVar_hsa_circ_112355,RMVar_hsa_circ_115228,RMVar_hsa_circ_196457,RMVar_hsa_circ_121548,RMVar_hsa_circ_196458,RMVar_hsa_circ_196459 15536 RMVar_ID_15536 Human_SNP_ID_670811220 A-to-I Human chr19 + 57845159 57845159 57845159 CCACCACACCACTAATGTTTTGTGGTTTTAGTAGAGACGGGTTTCACCGTGTTGCACAGACTGGT CCACCACACCACTAATGTTTTGTGGTTTTAGTGGAGACGGGTTTCACCGTGTTGCACAGACTGGT A G AC010522.1,ZNF587B Ensembl:ENSG00000268750,Ensembl:ENSG00000269343 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs745476040 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1892845,Human_RBP_ID_9928230,Human_RBP_ID_13523073 RMVar_hsa_circ_196453,RMVar_hsa_circ_121905,RMVar_hsa_circ_112355,RMVar_hsa_circ_115228,RMVar_hsa_circ_196457,RMVar_hsa_circ_121548,RMVar_hsa_circ_196458,RMVar_hsa_circ_196459 15537 RMVar_ID_15537 Human_SNP_ID_670811376 A-to-I Human chr19 + 57845860 57845860 57845860 GAAAAATAGCCAGGTATGGTGGCATGTACCTTAGTCTTAGTGATGTGGGAGGATTGCTTGAGCCT GAAAAATAGCCAGGTATGGTGGCATGTACCTTGGTCTTAGTGATGTGGGAGGATTGCTTGAGCCT A G AC010522.1,ZNF587B Ensembl:ENSG00000268750,Ensembl:ENSG00000269343 Protein coding,Protein coding intron,3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs3187122 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6790161,Human_RBP_ID_8495331 RMVar_hsa_circ_196453,RMVar_hsa_circ_121905,RMVar_hsa_circ_112355,RMVar_hsa_circ_115228,RMVar_hsa_circ_196457,RMVar_hsa_circ_121548,RMVar_hsa_circ_196458,RMVar_hsa_circ_196459 15538 RMVar_ID_15538 Human_SNP_ID_670811382 A-to-I Human chr19 + 57845900 57845900 57845900 TGATGTGGGAGGATTGCTTGAGCCTGGGAGGCAGAAGTTGCAGTGAGCTAAGATTGCAACGCTGC TGATGTGGGAGGATTGCTTGAGCCTGGGAGGCGGAAGTTGCAGTGAGCTAAGATTGCAACGCTGC A G AC010522.1,ZNF587B Ensembl:ENSG00000268750,Ensembl:ENSG00000269343 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1129340 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196453,RMVar_hsa_circ_121905,RMVar_hsa_circ_112355,RMVar_hsa_circ_115228,RMVar_hsa_circ_196457,RMVar_hsa_circ_121548,RMVar_hsa_circ_196458,RMVar_hsa_circ_196459 15539 RMVar_ID_15539 Human_SNP_ID_670811387 A-to-I Human chr19 + 57845917 57845917 57845917 TTGAGCCTGGGAGGCAGAAGTTGCAGTGAGCTAAGATTGCAACGCTGCAGTCCAGCCTGGGTGAT TTGAGCCTGGGAGGCAGAAGTTGCAGTGAGCTGAGATTGCAACGCTGCAGTCCAGCCTGGGTGAT A G AC010522.1,ZNF587B Ensembl:ENSG00000268750,Ensembl:ENSG00000269343 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs3177530 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25436339 RMVar_hsa_circ_196453,RMVar_hsa_circ_121905,RMVar_hsa_circ_112355,RMVar_hsa_circ_115228,RMVar_hsa_circ_196457,RMVar_hsa_circ_121548,RMVar_hsa_circ_196458,RMVar_hsa_circ_196459 15540 RMVar_ID_15540 Human_SNP_ID_670811389 A-to-I Human chr19 + 57845925 57845925 57845925 GGGAGGCAGAAGTTGCAGTGAGCTAAGATTGCAACGCTGCAGTCCAGCCTGGGTGATAGAGTGAG GGGAGGCAGAAGTTGCAGTGAGCTAAGATTGCGACGCTGCAGTCCAGCCTGGGTGATAGAGTGAG A G AC010522.1,ZNF587B Ensembl:ENSG00000268750,Ensembl:ENSG00000269343 Protein coding,Protein coding intron,3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1456442977 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25436339 RMVar_hsa_circ_196453,RMVar_hsa_circ_121905,RMVar_hsa_circ_112355,RMVar_hsa_circ_115228,RMVar_hsa_circ_196457,RMVar_hsa_circ_121548,RMVar_hsa_circ_196458,RMVar_hsa_circ_196459 15541 RMVar_ID_15541 Human_SNP_ID_670811398 A-to-I Human chr19 + 57845950 57845950 57845950 AGATTGCAACGCTGCAGTCCAGCCTGGGTGATAGAGTGAGACCCCATCTTAAAAATAAAATAAAG AGATTGCAACGCTGCAGTCCAGCCTGGGTGATGGAGTGAGACCCCATCTTAAAAATAAAATAAAG A G AC010522.1,ZNF587B Ensembl:ENSG00000268750,Ensembl:ENSG00000269343 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1129348 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196453,RMVar_hsa_circ_121905,RMVar_hsa_circ_112355,RMVar_hsa_circ_115228,RMVar_hsa_circ_196457,RMVar_hsa_circ_121548,RMVar_hsa_circ_196458,RMVar_hsa_circ_196459 15542 RMVar_ID_15542 Human_SNP_ID_670813604 A-to-I Human chr19 - 57852945 57852945 57852945 AGGAGGCTGAGGCAGGAGAATCACTTGAGCCCAGGAGGTGAAGGTTGCAGTGGGCTGAGATTGTG AGGAGGCTGAGGCAGGAGAATCACTTGAGCCCGGGAGGTGAAGGTTGCAGTGGGCTGAGATTGTG T C ZNF814 Ensembl:ENSG00000204514 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs541628865 Functional Loss SNV dbSNP153 33..33 33 - - - 15543 RMVar_ID_15543 Human_SNP_ID_670813950 A-to-I Human chr19 + 57853895 57853895 57853895 CTCCTGCCTCAGCCTCCCAAGTAGCTAGTATTACAGGCACCTGCCACCACAGCAGGCTAATTTTT CTCCTGCCTCAGCCTCCCAAGTAGCTAGTATTGCAGGCACCTGCCACCACAGCAGGCTAATTTTT A G ZNF587,AC010522.1 Ensembl:ENSG00000198466,Ensembl:ENSG00000268750 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1377944138 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196453,RMVar_hsa_circ_121905 15544 RMVar_ID_15544 Human_SNP_ID_670813951 A-to-I Human chr19 + 57853895 57853895 57853895 CTCCTGCCTCAGCCTCCCAAGTAGCTAGTATTACAGGCACCTGCCACCACAGCAGGCTAATTTTT CTCCTGCCTCAGCCTCCCAAGTAGCTAGTATTTCAGGCACCTGCCACCACAGCAGGCTAATTTTT A T ZNF587,AC010522.1 Ensembl:ENSG00000198466,Ensembl:ENSG00000268750 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1377944138 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196453,RMVar_hsa_circ_121905 15545 RMVar_ID_15545 Human_SNP_ID_670813970 A-to-I Human chr19 + 57853970 57853970 57853970 TAGAGACAGGGTTTCACCATGCTGACCAGGCTAGTCTTGAACTCCTGACCGGGTGATCTGCCTGC TAGAGACAGGGTTTCACCATGCTGACCAGGCTGGTCTTGAACTCCTGACCGGGTGATCTGCCTGC A G ZNF587,AC010522.1 Ensembl:ENSG00000198466,Ensembl:ENSG00000268750 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1467774361 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_772358,Human_RBP_ID_13523368 RMVar_hsa_circ_196453,RMVar_hsa_circ_121905 15546 RMVar_ID_15546 Human_SNP_ID_670814304 A-to-I Human chr19 + 57855116 57855116 57855116 TGAGGCAGGAGAATGGCCTGAACCTGGGAGGCAGAGCTTGCACTGAGCTGAGATCATGCTACTGC TGAGGCAGGAGAATGGCCTGAACCTGGGAGGCGGAGCTTGCACTGAGCTGAGATCATGCTACTGC A G ZNF587,AC010522.1 Ensembl:ENSG00000198466,Ensembl:ENSG00000268750 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs534720136 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23180716 RMVar_hsa_circ_196453,RMVar_hsa_circ_121905 15547 RMVar_ID_15547 Human_SNP_ID_670814381 A-to-I Human chr19 + 57855333 57855333 57855333 TGTTCCTGCACTCCAGCCTGGGTGGCAGAGCTAGACTATGTCTCAAAAAAATCCCCCAAAAATAA TGTTCCTGCACTCCAGCCTGGGTGGCAGAGCTTGACTATGTCTCAAAAAAATCCCCCAAAAATAA A T ZNF587,AC010522.1 Ensembl:ENSG00000198466,Ensembl:ENSG00000268750 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1352320621 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196453,RMVar_hsa_circ_121905 15548 RMVar_ID_15548 Human_SNP_ID_670814565 A-to-I Human chr19 + 57855763 57855763 57855763 TTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTAACCAGCATAGTCTCTATCCCCTGACTG TTTTGTATTTTTAGTAGAGACAGGGTTTCACCGTGTTAACCAGCATAGTCTCTATCCCCTGACTG A G ZNF587,AC010522.1 Ensembl:ENSG00000198466,Ensembl:ENSG00000268750 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1399254352 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23180721 RMVar_hsa_circ_196453,RMVar_hsa_circ_121905 15549 RMVar_ID_15549 Human_SNP_ID_670816370 A-to-I Human chr19 + 57860469 57860469 57860469 TTTTGTGTTTTTAGTGGAGATGGGGTTTTACCATGTTGGCCAGGCTGGTCTCAAACTCCTGACCT TTTTGTGTTTTTAGTGGAGATGGGGTTTTACCCTGTTGGCCAGGCTGGTCTCAAACTCCTGACCT A C ZNF587 Ensembl:ENSG00000198466 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,31158229,32596459 RNA-Seq:(High) rs563531374 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22477309 15550 RMVar_ID_15550 Human_SNP_ID_670816381 A-to-I Human chr19 + 57860528 57860528 57860528 TGACCTCAAGTGATCCACCCACCTTGACTCCCAAAGTGCTGAAATTACAGGCATGAGCCTCTGCA TGACCTCAAGTGATCCACCCACCTTGACTCCCTAAGTGCTGAAATTACAGGCATGAGCCTCTGCA A T ZNF587 Ensembl:ENSG00000198466 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1161920140 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1892884 15551 RMVar_ID_15551 Human_SNP_ID_670816491 A-to-I Human chr19 + 57860881 57860880 57860882 TGATAGATTAAAGTACAACTCTTTTTTGAGACAGAGTCTCACTCTGTCACCCAGGCGGGAGTTAG TGATAGATTAAAGTACAACTCTTTTTTGAGAC__AGTCTCACTCTGTCACCCAGGCGGGAGTTAG CAG C ZNF587 Ensembl:ENSG00000198466 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1190913426 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_13523506,Human_RBP_ID_17501877,Human_RBP_ID_25436404,Human_RBP_ID_26996350 Human_miRNA_ID_1534651 15552 RMVar_ID_15552 Human_SNP_ID_670816495 A-to-I Human chr19 + 57860889 57860889 57860889 TAAAGTACAACTCTTTTTTGAGACAGAGTCTCACTCTGTCACCCAGGCGGGAGTTAGGTGGCATG TAAAGTACAACTCTTTTTTGAGACAGAGTCTCTCTCTGTCACCCAGGCGGGAGTTAGGTGGCATG A T ZNF587 Ensembl:ENSG00000198466 Protein coding 3'UTR GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1218518539 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_773016,Human_RBP_ID_13523508,Human_RBP_ID_17501877,Human_RBP_ID_25436404,Human_RBP_ID_26996350 Human_miRNA_ID_867202 15553 RMVar_ID_15553 Human_SNP_ID_670816517 A-to-I Human chr19 + 57860937 57860937 57860937 GGGAGTTAGGTGGCATGATTTCGGCTCACTGCAACCTCTGCCTCCCAAGTTCAACTGATTCTTCT GGGAGTTAGGTGGCATGATTTCGGCTCACTGCGACCTCTGCCTCCCAAGTTCAACTGATTCTTCT A G ZNF587 Ensembl:ENSG00000198466 Protein coding 3'UTR GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1287935917 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27471973 15554 RMVar_ID_15554 Human_SNP_ID_670816642 A-to-I Human chr19 + 57861355 57861355 57861355 TTTATGTTTTGCATTTTTTTTGTTTTGAGACAAAGTCTCGCTCTGTCTCCCAGGCTAGAGTACCG TTTATGTTTTGCATTTTTTTTGTTTTGAGACATAGTCTCGCTCTGTCTCCCAGGCTAGAGTACCG A T ZNF587 Ensembl:ENSG00000198466 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs756628369 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2571368,Human_RBP_ID_6790263,Human_RBP_ID_23310007 15555 RMVar_ID_15555 Human_SNP_ID_670816648 A-to-I Human chr19 + 57861384 57861384 57861384 ACAAAGTCTCGCTCTGTCTCCCAGGCTAGAGTACCGTGGCACAATCTCAGCTCATTGCAACCTCT ACAAAGTCTCGCTCTGTCTCCCAGGCTAGAGTGCCGTGGCACAATCTCAGCTCATTGCAACCTCT A G ZNF587 Ensembl:ENSG00000198466 Protein coding 3'UTR GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,29796672,31158229,31158229,31158229,32596459,32596459 RNA-Seq:(High) rs1196623517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1892894,Human_RBP_ID_8495362,Human_RBP_ID_13523546 Human_Splice_Rec_2050827 RMVar_hsa_circ_90769,RMVar_hsa_circ_196462,RMVar_hsa_circ_87749,RMVar_hsa_circ_196461 15556 RMVar_ID_15556 Human_SNP_ID_670816656 A-to-I Human chr19 + 57861394 57861394 57861394 GCTCTGTCTCCCAGGCTAGAGTACCGTGGCACAATCTCAGCTCATTGCAACCTCTGCTTCCTGGG GCTCTGTCTCCCAGGCTAGAGTACCGTGGCACCATCTCAGCTCATTGCAACCTCTGCTTCCTGGG A C ZNF587 Ensembl:ENSG00000198466 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs1340826439 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8495362,Human_RBP_ID_26470610 Human_Splice_Rec_2050827 RMVar_hsa_circ_90769,RMVar_hsa_circ_196462,RMVar_hsa_circ_87749,RMVar_hsa_circ_196461 15557 RMVar_ID_15557 Human_SNP_ID_670816671 A-to-I Human chr19 + 57861430 57861430 57861430 TCAGCTCATTGCAACCTCTGCTTCCTGGGCTCAAGCACTCTGCCCACCTCAGCCTCCAGAGTAGC TCAGCTCATTGCAACCTCTGCTTCCTGGGCTCGAGCACTCTGCCCACCTCAGCCTCCAGAGTAGC A G ZNF587 Ensembl:ENSG00000198466 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037966724 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8495363,Human_RBP_ID_13523547 Human_Splice_Rec_2050827 Human_miRNA_ID_1642243,Human_miRNA_ID_2844071,Human_miRNA_ID_2874292,Human_miRNA_ID_2982252 RMVar_hsa_circ_90769,RMVar_hsa_circ_196462,RMVar_hsa_circ_87749,RMVar_hsa_circ_196461 15558 RMVar_ID_15558 Human_SNP_ID_670816851 A-to-I Human chr19 + 57861859 57861859 57861859 AAGTGGCATGATCTCGGCCCACTGCAACCTCCACCTCCTGTGTTCAAGCGATTCTGCCTCAGCCT AAGTGGCATGATCTCGGCCCACTGCAACCTCCCCCTCCTGTGTTCAAGCGATTCTGCCTCAGCCT A C ZNF587 Ensembl:ENSG00000198466 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1309498977 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13523580 Human_Splice_Rec_2050828 RMVar_hsa_circ_196462,RMVar_hsa_circ_87749 15559 RMVar_ID_15559 Human_SNP_ID_670816860 A-to-I Human chr19 + 57861887 57861887 57861887 CTCCACCTCCTGTGTTCAAGCGATTCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCATGTG CTCCACCTCCTGTGTTCAAGCGATTCTGCCTCGGCCTCCTGAGTAGCTGGGACTACAGGCATGTG A G ZNF587 Ensembl:ENSG00000198466 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1568510686 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2050828 RMVar_hsa_circ_196462,RMVar_hsa_circ_87749 15560 RMVar_ID_15560 Human_SNP_ID_670816894 A-to-I Human chr19 + 57862035 57862035 57862035 AGCTCAAGTGATCCACCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTCAGCCACTGTAC AGCTCAAGTGATCCACCTGCCTCGGCCTCCCAGAGTGCTGGGATTACAGGTGTCAGCCACTGTAC A G ZNF587 Ensembl:ENSG00000198466 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1294268271 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196462,RMVar_hsa_circ_87749 15561 RMVar_ID_15561 Human_SNP_ID_670817212 A-to-I Human chr19 + 57863032 57863013 57863032 TGGAGTGCAGTGGCACGATCTCGGCTCACTGCAACTCCACCTCCCGGGTTCACGCCATTCTCTTG TGGAGTGCAGTGGC___________________ACTCCACCTCCCGGGTTCACGCCATTCTCTTG CACGATCTCGGCTCACTGCA C ZNF587 Ensembl:ENSG00000198466 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1230173591 Functional Loss DEL dbSNP153 15..33 33 - - - Human_RBP_ID_772363,Human_RBP_ID_13523656 RMVar_hsa_circ_196462,RMVar_hsa_circ_87749 15562 RMVar_ID_15562 Human_SNP_ID_670817297 A-to-I Human chr19 + 57863235 57863235 57863235 ACCTCCTGGATTCAAGCACTTCTCCTTGCCTCAGCCACCTCTTTAGCTGGGATTACAGGTGCGTG ACCTCCTGGATTCAAGCACTTCTCCTTGCCTCCGCCACCTCTTTAGCTGGGATTACAGGTGCGTG A C ZNF587 Ensembl:ENSG00000198466 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985395286 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8495373,Human_RBP_ID_13523663,Human_RBP_ID_17932696,Human_RBP_ID_18740860,Human_RBP_ID_21930063 15563 RMVar_ID_15563 Human_SNP_ID_670817342 A-to-I Human chr19 + 57863478 57863345 57863478 TTACTGTATTTGCCAGGATGGTCTCGATCTCCAGACCTCGTGATCCGCCCGCCTTAGCCTCCCAA _________________________________GACCTCGTGATCCGCCCGCCTTAGCCTCCCAA TGACCTCGTGATCCACCCACCTCGGCCTCCCAAAGTGCTGGAATTACAGGCGTGAGCCACTGCACCTGGCCTGTATTCTTTTCTTTAGTAGAGACGGGGTTTTACTGTATTTGCCAGGATGGTCTCGATCTCCA T ZNF587 Ensembl:ENSG00000198466 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1568511491 Functional Loss DEL dbSNP153 1..33 33 - - - Human_RBP_ID_6790314,Human_RBP_ID_13523675 15564 RMVar_ID_15564 Human_SNP_ID_670817370 A-to-I Human chr19 - 57863524 57863391 57863524 AAGAAGTGGCCAGGGCGTGTTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCTAAGGCGGGC AAGAAGTGGCCAGGGCGTGTTGGCTCACGCCT_________________________________ CAGGCGTGAGCCACTGCACCTGGCCTGTATTCTTTTCTTTAGTAGAGACGGGGTTTTACTGTATTTGCCAGGATGGTCTCGATCTCCAGACCTCGTGATCCGCCCGCCTTAGCCTCCCAAAGTGCTGGGATTAT C ZNF814 Ensembl:ENSG00000204514 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1568511556 Functional Loss DEL dbSNP153 33..65 33 - - - 15565 RMVar_ID_15565 Human_SNP_ID_670817427 A-to-I Human chr19 + 57863478 57863478 57863478 TTACTGTATTTGCCAGGATGGTCTCGATCTCCAGACCTCGTGATCCGCCCGCCTTAGCCTCCCAA TTACTGTATTTGCCAGGATGGTCTCGATCTCCTGACCTCGTGATCCGCCCGCCTTAGCCTCCCAA A T ZNF587 Ensembl:ENSG00000198466 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1253196985 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6790314,Human_RBP_ID_13523675 15566 RMVar_ID_15566 Human_SNP_ID_670817440 A-to-I Human chr19 + 57863509 57863509 57863509 CAGACCTCGTGATCCGCCCGCCTTAGCCTCCCAAAGTGCTGGGATTATAGGCGTGAGCCAACACG CAGACCTCGTGATCCGCCCGCCTTAGCCTCCCGAAGTGCTGGGATTATAGGCGTGAGCCAACACG A G ZNF587 Ensembl:ENSG00000198466 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348082059 Functional Loss SNV dbSNP153 33..33 33 - - - 15567 RMVar_ID_15567 Human_SNP_ID_670817441 A-to-I Human chr19 + 57863510 57863510 57863510 AGACCTCGTGATCCGCCCGCCTTAGCCTCCCAAAGTGCTGGGATTATAGGCGTGAGCCAACACGC AGACCTCGTGATCCGCCCGCCTTAGCCTCCCAGAGTGCTGGGATTATAGGCGTGAGCCAACACGC A G ZNF587 Ensembl:ENSG00000198466 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1172054918 Functional Loss SNV dbSNP153 33..33 33 - - - 15568 RMVar_ID_15568 Human_SNP_ID_670817442 A-to-I Human chr19 + 57863510 57863510 57863510 AGACCTCGTGATCCGCCCGCCTTAGCCTCCCAAAGTGCTGGGATTATAGGCGTGAGCCAACACGC AGACCTCGTGATCCGCCCGCCTTAGCCTCCCATAGTGCTGGGATTATAGGCGTGAGCCAACACGC A T ZNF587 Ensembl:ENSG00000198466 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1172054918 Functional Loss SNV dbSNP153 33..33 33 - - - 15569 RMVar_ID_15569 Human_SNP_ID_670817446 A-to-I Human chr19 - 57863524 57863524 57863524 AAGAAGTGGCCAGGGCGTGTTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCTAAGGCGGGC AAGAAGTGGCCAGGGCGTGTTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTAAGGCGGGC T C ZNF814 Ensembl:ENSG00000204514 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs530322084 Functional Loss SNV dbSNP153 33..33 33 - - - 15570 RMVar_ID_15570 Human_SNP_ID_670817543 A-to-I Human chr19 + 57863767 57863767 57863767 CAAGATAATCAGCTATATGAAGAATCTTGGCCAGGTGTGGTGGCTGAGGCCTGTAATCCCACCAC CAAGATAATCAGCTATATGAAGAATCTTGGCCGGGTGTGGTGGCTGAGGCCTGTAATCCCACCAC A G ZNF587 Ensembl:ENSG00000198466 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs958248601 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13523710 15571 RMVar_ID_15571 Human_SNP_ID_670817553 A-to-I Human chr19 + 57863789 57863789 57863789 AATCTTGGCCAGGTGTGGTGGCTGAGGCCTGTAATCCCACCACTTTGGGAGGCTGAGGTGGGCGG AATCTTGGCCAGGTGTGGTGGCTGAGGCCTGTCATCCCACCACTTTGGGAGGCTGAGGTGGGCGG A C ZNF587 Ensembl:ENSG00000198466 Protein coding 3'UTR GSE38233;GSE100210;GSE100210;GSE99789;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,29129909,29796672,31158229,31158229 RNA-Seq:(High) rs1322819152 Functional Loss SNV dbSNP153 33..33 33 - - - 15572 RMVar_ID_15572 Human_SNP_ID_670817565 A-to-I Human chr19 + 57863827 57863827 57863827 ACCACTTTGGGAGGCTGAGGTGGGCGGATCACAAGGTCAGGAGTTCAAGACCACCCTGGCCAATA ACCACTTTGGGAGGCTGAGGTGGGCGGATCACGAGGTCAGGAGTTCAAGACCACCCTGGCCAATA A G ZNF587 Ensembl:ENSG00000198466 Protein coding 3'UTR GSE100210;GSE99789;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,29796672,32596459,32596459 RNA-Seq:(High) rs1471859117 Functional Loss SNV dbSNP153 33..33 33 - - - 15573 RMVar_ID_15573 Human_SNP_ID_670817575 A-to-I Human chr19 + 57863856 57863856 57863856 CACAAGGTCAGGAGTTCAAGACCACCCTGGCCAATATTGTGAATTCCTGTCTCTACTAAAAATAC CACAAGGTCAGGAGTTCAAGACCACCCTGGCCCATATTGTGAATTCCTGTCTCTACTAAAAATAC A C ZNF587 Ensembl:ENSG00000198466 Protein coding 3'UTR GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-Seq:(High) rs1265011789 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1191910,Human_RBP_ID_23180759,Human_RBP_ID_25436469 15574 RMVar_ID_15574 Human_SNP_ID_670817587 A-to-I Human chr19 + 57863881 57863881 57863881 CCTGGCCAATATTGTGAATTCCTGTCTCTACTAAAAATACAAAAATTAGTCGGGCATGGTGGCGG CCTGGCCAATATTGTGAATTCCTGTCTCTACTGAAAATACAAAAATTAGTCGGGCATGGTGGCGG A G ZNF587 Ensembl:ENSG00000198466 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1159575782 Functional Loss SNV dbSNP153 33..33 33 - - - 15575 RMVar_ID_15575 Human_SNP_ID_670817593 A-to-I Human chr19 + 57863904 57863904 57863904 GTCTCTACTAAAAATACAAAAATTAGTCGGGCATGGTGGCGGGTGCCTGTAGTCCCAGCTACTCG GTCTCTACTAAAAATACAAAAATTAGTCGGGCGTGGTGGCGGGTGCCTGTAGTCCCAGCTACTCG A G ZNF587 Ensembl:ENSG00000198466 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1245063071 Functional Loss SNV dbSNP153 33..33 33 - - - 15576 RMVar_ID_15576 Human_SNP_ID_670817604 A-to-I Human chr19 + 57863932 57863932 57863932 GGGCATGGTGGCGGGTGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCCAGAAAATCGGTTGAA GGGCATGGTGGCGGGTGCCTGTAGTCCCAGCTTCTCGGGAGGCTGAGGCCAGAAAATCGGTTGAA A T ZNF587 Ensembl:ENSG00000198466 Protein coding 3'UTR GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs1428004725 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8495374,Human_RBP_ID_17568190 15577 RMVar_ID_15577 Human_SNP_ID_670817617 A-to-I Human chr19 + 57863977 57863977 57863977 AGGCCAGAAAATCGGTTGAACCTGGGAGGTGGAAGGTGCACTGAGCCAATATCACACCAGTGCAC AGGCCAGAAAATCGGTTGAACCTGGGAGGTGGCAGGTGCACTGAGCCAATATCACACCAGTGCAC A C ZNF587 Ensembl:ENSG00000198466 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1289350867 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6790319,Human_RBP_ID_17568190,Human_RBP_ID_22476776 15578 RMVar_ID_15578 Human_SNP_ID_670817621 A-to-I Human chr19 + 57863992 57863992 57863992 TTGAACCTGGGAGGTGGAAGGTGCACTGAGCCAATATCACACCAGTGCACTCCAACCTGGTGACA TTGAACCTGGGAGGTGGAAGGTGCACTGAGCCGATATCACACCAGTGCACTCCAACCTGGTGACA A G ZNF587 Ensembl:ENSG00000198466 Protein coding 3'UTR GSE38233;GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,32596459 RNA-Seq:(High) rs1212375694 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17568190,Human_RBP_ID_22476776,Human_RBP_ID_23180760,Human_RBP_ID_25436473 15579 RMVar_ID_15579 Human_SNP_ID_670817627 A-to-I Human chr19 + 57864008 57864008 57864008 GAAGGTGCACTGAGCCAATATCACACCAGTGCACTCCAACCTGGTGACAGAGAGACACATCATCT GAAGGTGCACTGAGCCAATATCACACCAGTGCGCTCCAACCTGGTGACAGAGAGACACATCATCT A G ZNF587 Ensembl:ENSG00000198466 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1309842870 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13523714,Human_RBP_ID_17568190,Human_RBP_ID_23180760,Human_RBP_ID_25436473 15580 RMVar_ID_15580 Human_SNP_ID_670817777 A-to-I Human chr19 + 57864299 57864299 57864299 GGGCCTATAGGTTCCCTCCACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGCTTTCA GGGCCTATAGGTTCCCTCCACCACGCCCAGCTGATTTTTGTATTTTTAGTAGAGATGGGCTTTCA A G ZNF587 Ensembl:ENSG00000198466 Protein coding 3'UTR GSE47997;GSE100210;GSE100210 K562 cells&HepG2 cells;HepG2 cell line;HepG2 cell line - 23474544,29129909,29129909 RNA-Seq:(High) rs112688157 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17932699 15581 RMVar_ID_15581 Human_SNP_ID_670817781 A-to-I Human chr19 + 57864334 57864333 57864335 TTTTGTATTTTTAGTAGAGATGGGCTTTCACTACGTTAGCCAGGCTGGTCTCAAACTCCTGACCT TTTTGTATTTTTAGTAGAGATGGGCTTTCACCATGTTAGCCAGGCTGGTCTCAAACTCCTGACCT TAC CAT ZNF587 Ensembl:ENSG00000198466 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs796303352 Functional Loss MNV dbSNP153 32..34 33 - - - Human_miRNA_ID_148647,Human_miRNA_ID_292003 15582 RMVar_ID_15582 Human_SNP_ID_670817784 A-to-I Human chr19 + 57864339 57864339 57864341 TATTTTTAGTAGAGATGGGCTTTCACTACGTTAGCCAGGCTGGTCTCAAACTCCTGACCTCATGA TATTTTTAGTAGAGATGGGCTTTCACTACGTTGGTCAGGCTGGTCTCAAACTCCTGACCTCATGA AGC GGT ZNF587 Ensembl:ENSG00000198466 Protein coding 3'UTR GSE47997;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,31158229,31158229,31158229 RNA-Seq:(High) rs796920039 Functional Loss MNV dbSNP153 33..35 33 - - - Human_miRNA_ID_336633 15583 RMVar_ID_15583 Human_SNP_ID_670817785 A-to-I Human chr19 + 57864339 57864339 57864339 TATTTTTAGTAGAGATGGGCTTTCACTACGTTAGCCAGGCTGGTCTCAAACTCCTGACCTCATGA TATTTTTAGTAGAGATGGGCTTTCACTACGTTGGCCAGGCTGGTCTCAAACTCCTGACCTCATGA A G ZNF587 Ensembl:ENSG00000198466 Protein coding 3'UTR GSE47997;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,31158229,31158229,31158229 RNA-Seq:(High) rs903126431 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_336633 15584 RMVar_ID_15584 Human_SNP_ID_670817798 A-to-I Human chr19 + 57864368 57864368 57864368 GTTAGCCAGGCTGGTCTCAAACTCCTGACCTCATGATCCACCCCCCTCGGCCTCCTAAAGTGCTG GTTAGCCAGGCTGGTCTCAAACTCCTGACCTCGTGATCCACCCCCCTCGGCCTCCTAAAGTGCTG A G ZNF587 Ensembl:ENSG00000198466 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,29129909,29796672,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs1378629979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22720528 Human_miRNA_ID_1273826 15585 RMVar_ID_15585 Human_SNP_ID_670817963 A-to-I Human chr19 + 57864868 57864868 57864868 ATTAAAGAGCCTTCCTGGAAAATGGAGGTTGCAATCAGCCGAGATGGTGCCATCGCACTCTAGCC ATTAAAGAGCCTTCCTGGAAAATGGAGGTTGCCATCAGCCGAGATGGTGCCATCGCACTCTAGCC A C ZNF587 Ensembl:ENSG00000198466 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs906914370 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6790328,Human_RBP_ID_13523726,Human_RBP_ID_17010965,Human_RBP_ID_22976633,Human_RBP_ID_25436486,Human_RBP_ID_26470612 15586 RMVar_ID_15586 Human_SNP_ID_670817964 A-to-I Human chr19 + 57864868 57864868 57864868 ATTAAAGAGCCTTCCTGGAAAATGGAGGTTGCAATCAGCCGAGATGGTGCCATCGCACTCTAGCC ATTAAAGAGCCTTCCTGGAAAATGGAGGTTGCTATCAGCCGAGATGGTGCCATCGCACTCTAGCC A T ZNF587 Ensembl:ENSG00000198466 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs906914370 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6790328,Human_RBP_ID_13523726,Human_RBP_ID_17010965,Human_RBP_ID_22976633,Human_RBP_ID_25436486,Human_RBP_ID_26470612 15587 RMVar_ID_15587 Human_SNP_ID_670818157 A-to-I Human chr19 + 57865582 57865582 57865582 GCAAAAATTAGCACCTGTAATCCCAGCTACTCAGGAGGCTGAGGCATAGAATTGCTTGAACCTGG GCAAAAATTAGCACCTGTAATCCCAGCTACTCTGGAGGCTGAGGCATAGAATTGCTTGAACCTGG A T - - Other Unknown GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 29129909,30559470 RNA-Seq:(High) rs1276042315 Functional Loss SNV dbSNP153 33..33 33 - - - 15588 RMVar_ID_15588 Human_SNP_ID_670818176 A-to-I Human chr19 + 57865656 57865656 57865656 GTTGCAGTGAGTTAAGATCGTGGCACTGCACTACAGCATGGGCAACAGAGCAAGACTCTGTCTCA GTTGCAGTGAGTTAAGATCGTGGCACTGCACTGCAGCATGGGCAACAGAGCAAGACTCTGTCTCA A G - - Other Unknown GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs963163768 Functional Loss SNV dbSNP153 33..33 33 - - - 15589 RMVar_ID_15589 Human_SNP_ID_670818361 A-to-I Human chr19 + 57866010 57866008 57866010 TGGAGAGAATCTTGCTCTGCTGCCCAGGCTGGAATGCAGTAGCATGATCATGGCTCACTGCAGCC TGGAGAGAATCTTGCTCTGCTGCCCAGGCTG__ATGCAGTAGCATGATCATGGCTCACTGCAGCC GGA G lnc-ZNF587-1 RNACentral:URS00008BC15C lincRNA exon GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1284882736 Functional Loss DEL dbSNP153 32..33 33 - - - 15590 RMVar_ID_15590 Human_SNP_ID_670818519 A-to-I Human chr19 + 57866632 57866632 57866632 ATGAACCCAGGAGGCGGAGTTTGCAGTGAGCCAAGATCAGGCCACTGCACTCCAGCCTGGGCGAC ATGAACCCAGGAGGCGGAGTTTGCAGTGAGCCGAGATCAGGCCACTGCACTCCAGCCTGGGCGAC A G lnc-ZNF587-1 RNACentral:URS00008BC15C lincRNA exon GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1251696855 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9928355,Human_RBP_ID_25448365 15591 RMVar_ID_15591 Human_SNP_ID_670818631 A-to-I Human chr19 + 57867012 57867012 57867012 TAAGCTGTGATCATGCCATTGCCCTCCAGCCTAGGCAACAGAGCTAGATCCTTGTCTTAAAAAAA TAAGCTGTGATCATGCCATTGCCCTCCAGCCTGGGCAACAGAGCTAGATCCTTGTCTTAAAAAAA A G lnc-ZNF587-1 RNACentral:URS00008BC15C lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs960636958 Functional Loss SNV dbSNP153 33..33 33 - - - 15592 RMVar_ID_15592 Human_SNP_ID_670818867 A-to-I Human chr19 + 57867607 57867607 57867607 CAGAGCCACCGCATTATTTTTCAGCCAGGTGCAGTGGCTCACACCTGTAACCCCGCACTTTGGGA CAGAGCCACCGCATTATTTTTCAGCCAGGTGCTGTGGCTCACACCTGTAACCCCGCACTTTGGGA A T - - Other Unknown GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1407181349 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23180783,Human_RBP_ID_26996370 15593 RMVar_ID_15593 Human_SNP_ID_670818926 A-to-I Human chr19 + 57867798 57867796 57867798 TACTCGGGAGGCTGAGGCAAGAGGATGGCTTGAACTCAGGAGGCAGAGGTTGTGGTGAGCCGAGA TACTCGGGAGGCTGAGGCAAGAGGATGGCTT__ACTCAGGAGGCAGAGGTTGTGGTGAGCCGAGA TGA T - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1253316431 Functional Loss DEL dbSNP153 32..33 33 - - - 15594 RMVar_ID_15594 Human_SNP_ID_670819143 A-to-I Human chr19 + 57868485 57868485 57868485 AGTACCTGCAAGGGTCAGGCGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGT AGTACCTGCAAGGGTCAGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGT A G AC010326.4 Ensembl:ENSG00000270804 Pseudogene exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs747571111 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17502712,Human_RBP_ID_22391460 15595 RMVar_ID_15595 Human_SNP_ID_670819409 A-to-I Human chr19 + 57869173 57869173 57869173 AAAAAATTAGCCGGGCGTGGTGGCGGGTGCCTATAGTCCCAGCTGCTCGGGAGGCTGAGGCAGGA AAAAAATTAGCCGGGCGTGGTGGCGGGTGCCTGTAGTCCCAGCTGCTCGGGAGGCTGAGGCAGGA A G - - Other Unknown GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs938856165 Functional Loss SNV dbSNP153 33..33 33 - - - 15596 RMVar_ID_15596 Human_SNP_ID_670819546 A-to-I Human chr19 + 57869463 57869463 57869463 GGAAAGTACTCTACTGTACAGCAAAGTAAATCATTGGTTGTCTGGAGAACAGAAAGAAAGCCTTT GGAAAGTACTCTACTGTACAGCAAAGTAAATCGTTGGTTGTCTGGAGAACAGAAAGAAAGCCTTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs921381786 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8495395,Human_RBP_ID_13523871,Human_RBP_ID_22503874 15597 RMVar_ID_15597 Human_SNP_ID_670820660 A-to-I Human chr19 + 57872942 57872942 57872942 GGCTTTTCTCCAGTGTGAACTCTCTTGTGTTTAGTGAGACTGGAGCTTTCAGCAAAAGATTTTCC GGCTTTTCTCCAGTGTGAACTCTCTTGTGTTTTGTGAGACTGGAGCTTTCAGCAAAAGATTTTCC A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs748331371 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_13523911 15598 RMVar_ID_15598 Human_SNP_ID_670820685 A-to-I Human chr19 + 57872992 57872992 57872992 AGCAAAAGATTTTCCACATTCACTGCACTCATAAGGCTTTTCTCCAGTGTGAACTCTTTTGTGTT AGCAAAAGATTTTCCACATTCACTGCACTCATGAGGCTTTTCTCCAGTGTGAACTCTTTTGTGTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs376088604 Functional Loss SNV dbSNP153 33..33 33 - - - 15599 RMVar_ID_15599 Human_SNP_ID_670824090 A-to-I Human chr19 - 57883400 57883400 57883400 CCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCATCATGCCTGGCCAGTTCTATTTTTT CCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCATCATGCCTGGCCAGTTCTATTTTTT T C ZNF814,AC010326.2 Ensembl:ENSG00000204514,Ensembl:ENSG00000269476 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1244205041 Functional Loss SNV dbSNP153 33..33 33 - - - 15600 RMVar_ID_15600 Human_SNP_ID_670827270 A-to-I Human chr19 - 57895141 57895141 57895141 GAGGCCCCTCTCAGTAAAGTCCCTCTTGGCTAAGAACTGGTTTGGCACCACAGGATGTCAACTTT GAGGCCCCTCTCAGTAAAGTCCCTCTTGGCTAGGAACTGGTTTGGCACCACAGGATGTCAACTTT T C AC010326.2 Ensembl:ENSG00000269476 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1044359521 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13523966 RMVar_hsa_circ_9920 15601 RMVar_ID_15601 Human_SNP_ID_670828612 A-to-I Human chr19 - 57900878 57900878 57900878 TGGTCACTGCACTCCAGCCTGGGCGACAGAGCAAGACTCCGTCTCAAAAAAAAAAAAAAAAAAAA TGGTCACTGCACTCCAGCCTGGGCGACAGAGCGAGACTCCGTCTCAAAAAAAAAAAAAAAAAAAA T C ZNF417,AC010326.2 Ensembl:ENSG00000173480,Ensembl:ENSG00000269476 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs544018784 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9920 15602 RMVar_ID_15602 Human_SNP_ID_670829169 A-to-I Human chr19 - 57902817 57902817 57902817 ATAAATAAAAAGCCACAAAAAATTAGCCGGGCATGGTGGTGGGCGCCTGTAGTCCCAGCTACTCG ATAAATAAAAAGCCACAAAAAATTAGCCGGGCGTGGTGGTGGGCGCCTGTAGTCCCAGCTACTCG T C ZNF417,AC010326.2 Ensembl:ENSG00000173480,Ensembl:ENSG00000269476 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459231219 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9920 15603 RMVar_ID_15603 Human_SNP_ID_670829215 A-to-I Human chr19 - 57902952 57902952 57902952 ATTTCCGGCCTGGCGGGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGCGGCGGGCGG ATTTCCGGCCTGGCGGGGTGGCTCACACCTGTGATCCCAGCACTTTGGGAGGCTGCGGCGGGCGG T C ZNF417,AC010326.2 Ensembl:ENSG00000173480,Ensembl:ENSG00000269476 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1455279889 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9920 15604 RMVar_ID_15604 Human_SNP_ID_670829706 A-to-I Human chr19 - 57904807 57904807 57904807 ACCTCAGGTGATCCGCCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGGGCCACCACTC ACCTCAGGTGATCCGCCCGCCTTGGCCTCCCAGAGTGCTGGGATTACAGGCGTGGGCCACCACTC T C ZNF417,AC010326.2 Ensembl:ENSG00000173480,Ensembl:ENSG00000269476 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs994011313 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9920 15605 RMVar_ID_15605 Human_SNP_ID_670829767 A-to-I Human chr19 - 57905034 57905034 57905034 TTTTTTTTTTTTTTTTTTTGAGACGGAGTTTCACTCTTGTTGCCCAGGCTGGAGTGCAATGGCAC TTTTTTTTTTTTTTTTTTTGAGACGGAGTTTCTCTCTTGTTGCCCAGGCTGGAGTGCAATGGCAC T A ZNF417,AC010326.2 Ensembl:ENSG00000173480,Ensembl:ENSG00000269476 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1339834865 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6806647 RMVar_hsa_circ_9920 15606 RMVar_ID_15606 Human_SNP_ID_670829882 A-to-I Human chr19 - 57905367 57905367 57905367 AGTTTCACTCTTACTGCCCAGGCTGGAGTGCAATGGTGAAATCTTGGCTTACTGCAACCTCCGCC AGTTTCACTCTTACTGCCCAGGCTGGAGTGCAGTGGTGAAATCTTGGCTTACTGCAACCTCCGCC T C ZNF417,AC010326.2 Ensembl:ENSG00000173480,Ensembl:ENSG00000269476 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1229864092 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9920 15607 RMVar_ID_15607 Human_SNP_ID_670829889 A-to-I Human chr19 - 57905393 57905393 57905393 TTTGGCTAAGATCAAGTGTGAGACGCAGTTTCACTCTTACTGCCCAGGCTGGAGTGCAATGGTGA TTTGGCTAAGATCAAGTGTGAGACGCAGTTTCTCTCTTACTGCCCAGGCTGGAGTGCAATGGTGA T A ZNF417,AC010326.2 Ensembl:ENSG00000173480,Ensembl:ENSG00000269476 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1188890042 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9920 15608 RMVar_ID_15608 Human_SNP_ID_670830168 A-to-I Human chr19 - 57906528 57906528 57906528 TCAAACTTGTGACCTCATGATCCACCCCCCTCAGCCTCCTAAAGTGCTGGGATTACAGGCATCTG TCAAACTTGTGACCTCATGATCCACCCCCCTCGGCCTCCTAAAGTGCTGGGATTACAGGCATCTG T C ZNF417,AC010326.2 Ensembl:ENSG00000173480,Ensembl:ENSG00000269476 Protein coding,Protein coding intron,intron GSE38233;GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs549446972 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9920,RMVar_hsa_circ_196465,RMVar_hsa_circ_94305 15609 RMVar_ID_15609 Human_SNP_ID_670830178 A-to-I Human chr19 - 57906544 57906544 57906544 GTTAGCCAGGCTGGTCTCAAACTTGTGACCTCATGATCCACCCCCCTCAGCCTCCTAAAGTGCTG GTTAGCCAGGCTGGTCTCAAACTTGTGACCTCGTGATCCACCCCCCTCAGCCTCCTAAAGTGCTG T C ZNF417,AC010326.2 Ensembl:ENSG00000173480,Ensembl:ENSG00000269476 Protein coding,Protein coding intron,intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs1268654276 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9920,RMVar_hsa_circ_196465,RMVar_hsa_circ_94305 15610 RMVar_ID_15610 Human_SNP_ID_670830179 A-to-I Human chr19 - 57906544 57906544 57906544 GTTAGCCAGGCTGGTCTCAAACTTGTGACCTCATGATCCACCCCCCTCAGCCTCCTAAAGTGCTG GTTAGCCAGGCTGGTCTCAAACTTGTGACCTCCTGATCCACCCCCCTCAGCCTCCTAAAGTGCTG T G ZNF417,AC010326.2 Ensembl:ENSG00000173480,Ensembl:ENSG00000269476 Protein coding,Protein coding intron,intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs1268654276 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9920,RMVar_hsa_circ_196465,RMVar_hsa_circ_94305 15611 RMVar_ID_15611 Human_SNP_ID_670830331 A-to-I Human chr19 - 57906890 57906890 57906890 GAGATTGCACCACTGCACTCCAGCCTGGTGACAGAGCGAGACTCCGTCTCAAAAAAAAAAAAAAA GAGATTGCACCACTGCACTCCAGCCTGGTGACGGAGCGAGACTCCGTCTCAAAAAAAAAAAAAAA T C ZNF417,AC010326.2 Ensembl:ENSG00000173480,Ensembl:ENSG00000269476 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1416734541 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9920,RMVar_hsa_circ_196465,RMVar_hsa_circ_94305 15612 RMVar_ID_15612 Human_SNP_ID_670830350 A-to-I Human chr19 - 57906992 57906992 57906992 AAAATTACCCAAGCATAGTGGTGGGTGCCTGTAGTCCCAGCTGCTTGGGAGGCTGAGGCAGGAGA AAAATTACCCAAGCATAGTGGTGGGTGCCTGTCGTCCCAGCTGCTTGGGAGGCTGAGGCAGGAGA T G ZNF417,AC010326.2 Ensembl:ENSG00000173480,Ensembl:ENSG00000269476 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1021440864 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9920,RMVar_hsa_circ_196465,RMVar_hsa_circ_94305 15613 RMVar_ID_15613 Human_SNP_ID_670830370 A-to-I Human chr19 - 57907073 57907072 57907074 CTGAGGTGGGTGGCTTACAAGGTCAGGAGTTCAAGACCACCCTGGACAATATGGTGAAACCCTGT CTGAGGTGGGTGGCTTACAAGGTCAGGAGTT__AGACCACCCTGGACAATATGGTGAAACCCTGT TTG T ZNF417,AC010326.2 Ensembl:ENSG00000173480,Ensembl:ENSG00000269476 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1555779056 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_9920,RMVar_hsa_circ_196465,RMVar_hsa_circ_94305 15614 RMVar_ID_15614 Human_SNP_ID_670830371 A-to-I Human chr19 - 57907073 57907073 57907073 CTGAGGTGGGTGGCTTACAAGGTCAGGAGTTCAAGACCACCCTGGACAATATGGTGAAACCCTGT CTGAGGTGGGTGGCTTACAAGGTCAGGAGTTCGAGACCACCCTGGACAATATGGTGAAACCCTGT T C ZNF417,AC010326.2 Ensembl:ENSG00000173480,Ensembl:ENSG00000269476 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs940307662 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9920,RMVar_hsa_circ_196465,RMVar_hsa_circ_94305 15615 RMVar_ID_15615 Human_SNP_ID_670839353 A-to-I Human chr19 - 57936267 57936267 57936267 GCAGGTGCAGCTAGTTCTAGGCAAGATGAGGCAGCACACAGGCCACGTCCTCACTCCTGTGGTAA GCAGGTGCAGCTAGTTCTAGGCAAGATGAGGCGGCACACAGGCCACGTCCTCACTCCTGTGGTAA T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs551091382 Functional Loss SNV dbSNP153 33..33 33 - - - 15616 RMVar_ID_15616 Human_SNP_ID_670840691 A-to-I Human chr19 - 57941243 57941243 57941243 AGTTCACACTGGAGAAAGGCCTTATGAGTGCAATGAATGTGGGAAGTTTTTTAGCCAGAGCTCCA AGTTCACACTGGAGAAAGGCCTTATGAGTGCAGTGAATGTGGGAAGTTTTTTAGCCAGAGCTCCA T C ZNF256 Ensembl:ENSG00000152454 Protein coding CDS GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs758292773 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_23809687 15617 RMVar_ID_15617 Human_SNP_ID_670887521 A-to-I Human chr19 - 58096133 58096133 58096133 CCAACTCCTGGGCTCAAGCAGTCCTCCTGCTTAAGACTCCCCAGGCTCTGAGATTATAGATGTAC CCAACTCCTGGGCTCAAGCAGTCCTCCTGCTTGAGACTCCCCAGGCTCTGAGATTATAGATGTAC T C ZSCAN18 Ensembl:ENSG00000121413 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1473811420 Functional Loss SNV dbSNP153 33..33 33 - - - 15618 RMVar_ID_15618 Human_SNP_ID_670895928 A-to-I Human chr19 - 58126774 58126774 58126774 TAGTGTGTGCCTGTAATCCCAGCTACTTGGGAAGCTGAGGCAGGAGAATTGCTTGAACCTGGGAG TAGTGTGTGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATTGCTTGAACCTGGGAG T C ZNF329 Ensembl:ENSG00000181894 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1309819317 Functional Loss SNV dbSNP153 33..33 33 - - - 15619 RMVar_ID_15619 Human_SNP_ID_670895931 A-to-I Human chr19 - 58126786 58126786 58126786 ATCTGGGCATAGTAGTGTGTGCCTGTAATCCCAGCTACTTGGGAAGCTGAGGCAGGAGAATTGCT ATCTGGGCATAGTAGTGTGTGCCTGTAATCCCGGCTACTTGGGAAGCTGAGGCAGGAGAATTGCT T C ZNF329 Ensembl:ENSG00000181894 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1315976487 Functional Loss SNV dbSNP153 33..33 33 - - - 15620 RMVar_ID_15620 Human_SNP_ID_670895936 A-to-I Human chr19 - 58126805 58126805 58126805 ACCAAAAATACAGGAAATTATCTGGGCATAGTAGTGTGTGCCTGTAATCCCAGCTACTTGGGAAG ACCAAAAATACAGGAAATTATCTGGGCATAGTGGTGTGTGCCTGTAATCCCAGCTACTTGGGAAG T C ZNF329 Ensembl:ENSG00000181894 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1346828558 Functional Loss SNV dbSNP153 33..33 33 - - - 15621 RMVar_ID_15621 Human_SNP_ID_670895937 A-to-I Human chr19 - 58126808 58126808 58126808 TCTACCAAAAATACAGGAAATTATCTGGGCATAGTAGTGTGTGCCTGTAATCCCAGCTACTTGGG TCTACCAAAAATACAGGAAATTATCTGGGCATGGTAGTGTGTGCCTGTAATCCCAGCTACTTGGG T C ZNF329 Ensembl:ENSG00000181894 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1026565788 Functional Loss SNV dbSNP153 33..33 33 - - - 15622 RMVar_ID_15622 Human_SNP_ID_670895958 A-to-I Human chr19 - 58126887 58126887 58126887 GCACTTTGGGAGGCCGAGGCGGCCAGATCACAAGGTTAGGAGTTCAAGACCAGCCTGGCCAGCAT GCACTTTGGGAGGCCGAGGCGGCCAGATCACAGGGTTAGGAGTTCAAGACCAGCCTGGCCAGCAT T C ZNF329 Ensembl:ENSG00000181894 Protein coding 3'UTR GSE47997;GSE107867 K562 cells&HepG2 cells;ASD brains,cerebellum - 23474544,30559470 RNA-Seq:(High) rs1029498768 Functional Loss SNV dbSNP153 33..33 33 - - - 15623 RMVar_ID_15623 Human_SNP_ID_670895969 A-to-I Human chr19 - 58126926 58126926 58126926 CAAGCAGGCCAGATGTGGTGGCTCACGCCTGTAATCCTAGCACTTTGGGAGGCCGAGGCGGCCAG CAAGCAGGCCAGATGTGGTGGCTCACGCCTGTGATCCTAGCACTTTGGGAGGCCGAGGCGGCCAG T C ZNF329 Ensembl:ENSG00000181894 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1488413554 Functional Loss SNV dbSNP153 33..33 33 - - - 15624 RMVar_ID_15624 Human_SNP_ID_670896042 A-to-I Human chr19 - 58127246 58127246 58127246 CGCCCACCTCAGCCTCCCAAAGTGTTGGGATTACAGGCATGAGACACTGCCTGGCCTGAATCAAC CGCCCACCTCAGCCTCCCAAAGTGTTGGGATTGCAGGCATGAGACACTGCCTGGCCTGAATCAAC T C ZNF329 Ensembl:ENSG00000181894 Protein coding 3'UTR GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1456001539 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196485 15625 RMVar_ID_15625 Human_SNP_ID_670896066 A-to-I Human chr19 - 58127338 58127338 58127338 GCCACCATGCCTGGCTAATTTTTTCTATTTTTAGTAGAGACAGGGTTTCACTGTGTTGGCCAGGC GCCACCATGCCTGGCTAATTTTTTCTATTTTTGGTAGAGACAGGGTTTCACTGTGTTGGCCAGGC T C ZNF329 Ensembl:ENSG00000181894 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs957167022 Functional Loss SNV dbSNP153 33..33 33 - - - 15626 RMVar_ID_15626 Human_SNP_ID_670896067 A-to-I Human chr19 - 58127338 58127338 58127338 GCCACCATGCCTGGCTAATTTTTTCTATTTTTAGTAGAGACAGGGTTTCACTGTGTTGGCCAGGC GCCACCATGCCTGGCTAATTTTTTCTATTTTTCGTAGAGACAGGGTTTCACTGTGTTGGCCAGGC T G ZNF329 Ensembl:ENSG00000181894 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs957167022 Functional Loss SNV dbSNP153 33..33 33 - - - 15627 RMVar_ID_15627 Human_SNP_ID_670896089 A-to-I Human chr19 - 58127416 58127416 58127416 CTCACAGCAACCTCTGCCTCCCAGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCAAAGTAGCTAGG CTCACAGCAACCTCTGCCTCCCAGGTTCAAGCGGTTCTCCTGCCTCAGCCTCCAAAGTAGCTAGG T C ZNF329 Ensembl:ENSG00000181894 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1303096115 Functional Loss SNV dbSNP153 33..33 33 - - - 15628 RMVar_ID_15628 Human_SNP_ID_670896091 A-to-I Human chr19 - 58127419 58127419 58127419 CCACTCACAGCAACCTCTGCCTCCCAGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCAAAGTAGCT CCACTCACAGCAACCTCTGCCTCCCAGGTTCAGGCAGTTCTCCTGCCTCAGCCTCCAAAGTAGCT T C ZNF329 Ensembl:ENSG00000181894 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1365829952 Functional Loss SNV dbSNP153 33..33 33 - - - 15629 RMVar_ID_15629 Human_SNP_ID_670912654 A-to-I Human chr19 + 58184443 58184443 58184443 TCCCCGAGTAGCTGGGACTACAGGCGTGTGCCACCATACCCAGCTAATTTTTTTTTTATTTTTAT TCCCCGAGTAGCTGGGACTACAGGCGTGTGCCGCCATACCCAGCTAATTTTTTTTTTATTTTTAT A G ZNF274 Ensembl:ENSG00000171606 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1456949625 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_138562,Human_RBP_ID_6790990 RMVar_hsa_circ_13258 15630 RMVar_ID_15630 Human_SNP_ID_670913503 A-to-I Human chr19 + 58187491 58187491 58187491 TCACCGAGGCTGGAGTGCAGTGGCATGATCTCAGCTCACTGCACCCTCCGCGTCCTGGACTCAAG TCACCGAGGCTGGAGTGCAGTGGCATGATCTCTGCTCACTGCACCCTCCGCGTCCTGGACTCAAG A T ZNF274 Ensembl:ENSG00000171606 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs939127816 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13524648,Human_RBP_ID_23310012 15631 RMVar_ID_15631 Human_SNP_ID_670915422 A-to-I Human chr19 + 58194508 58194508 58194508 TCAGGCAATTCTCCTGCCTCAGCCTTCTGTGTAGCTGGGACTACAGGCACCTGCCACCACACCTA TCAGGCAATTCTCCTGCCTCAGCCTTCTGTGTCGCTGGGACTACAGGCACCTGCCACCACACCTA A C ZNF274 Ensembl:ENSG00000171606 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs925824462 Functional Loss SNV dbSNP153 33..33 33 - - - 15632 RMVar_ID_15632 Human_SNP_ID_670926644 A-to-I Human chr19 + 58237298 58237298 58237298 GTTGCCTAGGCTTGTCTTGATCTCCTCGGCTCAAGCAGTCCGCCTGCCTCTGCTGCCCAGAGTTT GTTGCCTAGGCTTGTCTTGATCTCCTCGGCTCCAGCAGTCCGCCTGCCTCTGCTGCCCAGAGTTT A C ZNF544,AC020915.5 Ensembl:ENSG00000198131,Ensembl:ENSG00000283515 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947195767 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2051422,Human_Splice_Rec_2051423 RMVar_hsa_circ_100464,RMVar_hsa_circ_93407,RMVar_hsa_circ_196492,RMVar_hsa_circ_196493 15633 RMVar_ID_15633 Human_SNP_ID_670927282 A-to-I Human chr19 + 58239778 58239778 58239778 AAAATTAGCCAGGTGTGGTGGCTTGCACTTGTAGTCCCAGTTACTTGGGAGGCTGAGACAGGAGA AAAATTAGCCAGGTGTGGTGGCTTGCACTTGTGGTCCCAGTTACTTGGGAGGCTGAGACAGGAGA A G ZNF544,AC020915.5 Ensembl:ENSG00000198131,Ensembl:ENSG00000283515 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs746439745 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100464,RMVar_hsa_circ_93407,RMVar_hsa_circ_196492,RMVar_hsa_circ_196493 15634 RMVar_ID_15634 Human_SNP_ID_670927421 A-to-I Human chr19 + 58240281 58240280 58240282 TTCTTTTTCTTTCTTTTTTTTTTTTTGGAGACAGAGTTTTGCTCTGTCGCCCAGGCTGGAGTGCA TTCTTTTTCTTTCTTTTTTTTTTTTTGGAGAC__AGTTTTGCTCTGTCGCCCAGGCTGGAGTGCA CAG C ZNF544,AC020915.5 Ensembl:ENSG00000198131,Ensembl:ENSG00000283515 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1228274299 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_100464,RMVar_hsa_circ_93407,RMVar_hsa_circ_196492,RMVar_hsa_circ_196493 15635 RMVar_ID_15635 Human_SNP_ID_670927423 A-to-I Human chr19 + 58240281 58240281 58240281 TTCTTTTTCTTTCTTTTTTTTTTTTTGGAGACAGAGTTTTGCTCTGTCGCCCAGGCTGGAGTGCA TTCTTTTTCTTTCTTTTTTTTTTTTTGGAGACGGAGTTTTGCTCTGTCGCCCAGGCTGGAGTGCA A G ZNF544,AC020915.5 Ensembl:ENSG00000198131,Ensembl:ENSG00000283515 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs964850143 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100464,RMVar_hsa_circ_93407,RMVar_hsa_circ_196492,RMVar_hsa_circ_196493 15636 RMVar_ID_15636 Human_SNP_ID_670927452 A-to-I Human chr19 + 58240387 58240387 58240387 TCACGCCATTCTCCTGCCTCAACTTCCCGAGTAGCTGGCACTACAGGCACCCACCACCACGCCCG TCACGCCATTCTCCTGCCTCAACTTCCCGAGTTGCTGGCACTACAGGCACCCACCACCACGCCCG A T ZNF544,AC020915.5 Ensembl:ENSG00000198131,Ensembl:ENSG00000283515 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1410442358 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100464,RMVar_hsa_circ_93407,RMVar_hsa_circ_196492,RMVar_hsa_circ_196493 15637 RMVar_ID_15637 Human_SNP_ID_670927525 A-to-I Human chr19 + 58240655 58240655 58240655 ATTGTGATGCGCGCCTGTGATCCCAGCTACTCAAGAGGCTGAGGCAGGAGAATCGCTTGAACCTG ATTGTGATGCGCGCCTGTGATCCCAGCTACTCGAGAGGCTGAGGCAGGAGAATCGCTTGAACCTG A G ZNF544,AC020915.5 Ensembl:ENSG00000198131,Ensembl:ENSG00000283515 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1052757031 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100464,RMVar_hsa_circ_93407,RMVar_hsa_circ_196492,RMVar_hsa_circ_196493 15638 RMVar_ID_15638 Human_SNP_ID_670928482 A-to-I Human chr19 + 58243606 58243606 58243606 GCTGGGGAGTGTCACATCCTCCTTGTCCCCACACCCCCATTGTCATCATTTCTGAAAACAGCTTA GCTGGGGAGTGTCACATCCTCCTTGTCCCCACGCCCCCATTGTCATCATTTCTGAAAACAGCTTA A G ZNF544,AC020915.5 Ensembl:ENSG00000198131,Ensembl:ENSG00000283515 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs260485 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100464,RMVar_hsa_circ_69347,RMVar_hsa_circ_93407,RMVar_hsa_circ_196492,RMVar_hsa_circ_196493 15639 RMVar_ID_15639 Human_SNP_ID_670931002 A-to-I Human chr19 + 58253464 58253464 58253464 AGTCTGATTTGTTTATTTATTTTTTGAGACAGAGCCTTGCTCTTTTGCCCAGGCTGGAGTACAGA AGTCTGATTTGTTTATTTATTTTTTGAGACAGGGCCTTGCTCTTTTGCCCAGGCTGGAGTACAGA A G ZNF544,AC020915.5 Ensembl:ENSG00000198131,Ensembl:ENSG00000283515 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1394798430 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93407,RMVar_hsa_circ_196493 15640 RMVar_ID_15640 Human_SNP_ID_670932832 A-to-I Human chr19 + 58259793 58259793 58259793 ATTTTTAGCAGGGTGTGGTAGCAGGCACCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGG ATTTTTAGCAGGGTGTGGTAGCAGGCACCTGTGATCCCAGCTACTCAGGAGGCTGAGGCAGGAGG A G ZNF544,AC020915.5 Ensembl:ENSG00000198131,Ensembl:ENSG00000283515 Protein coding,Protein coding intron,intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1418120769 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2891288 RMVar_hsa_circ_93407,RMVar_hsa_circ_196493 15641 RMVar_ID_15641 Human_SNP_ID_670932966 A-to-I Human chr19 + 58260416 58260416 58260416 CTCCTGCCTCGGCCTCCCGAGGAGCTTAGACTACAGGCGCCCACCACCACACCTGGCTAATTTTT CTCCTGCCTCGGCCTCCCGAGGAGCTTAGACTGCAGGCGCCCACCACCACACCTGGCTAATTTTT A G ZNF544,AC020915.5 Ensembl:ENSG00000198131,Ensembl:ENSG00000283515 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1199240511 Functional Loss SNV dbSNP153 33..33 33 - - - 15642 RMVar_ID_15642 Human_SNP_ID_670934134 A-to-I Human chr19 + 58263354 58263354 58263354 ATGGTGGCGCATACCTGTAGTCCTAGCTACTCAGGAGGCTGAGGTGGGAGGATCACTTGAGCTTG ATGGTGGCGCATACCTGTAGTCCTAGCTACTCGGGAGGCTGAGGTGGGAGGATCACTTGAGCTTG A G ZNF544,AC020915.5 Ensembl:ENSG00000198131,Ensembl:ENSG00000283515 Protein coding,Protein coding 3'UTR,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1009013974 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22719321 RMVar_hsa_circ_196496,RMVar_hsa_circ_196495,RMVar_hsa_circ_269509 15643 RMVar_ID_15643 Human_SNP_ID_670934381 A-to-I Human chr19 + 58264316 58264316 58264316 GGCTGAGGCAGGAGAATCTTGACCTGGGAGGCAGAGGTTGCAGTGAACCAAGATCAAGCCATTGT GGCTGAGGCAGGAGAATCTTGACCTGGGAGGCGGAGGTTGCAGTGAACCAAGATCAAGCCATTGT A G ZNF544,AC020915.5 Ensembl:ENSG00000198131,Ensembl:ENSG00000283515 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1265241539 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17567841,Human_RBP_ID_23180901 15644 RMVar_ID_15644 Human_SNP_ID_670934705 A-to-I Human chr19 - 58265434 58265434 58265434 AAAATTAGACAGACGTGGTGACGGGTGCCTGTAGTCCCAGCTACTCAGCAGGTTGAGGCAGGAGA AAAATTAGACAGACGTGGTGACGGGTGCCTGTGGTCCCAGCTACTCAGCAGGTTGAGGCAGGAGA T C AC020915.3 Ensembl:ENSG00000268516 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs964605780 Functional Loss SNV dbSNP153 33..33 33 - - - 15645 RMVar_ID_15645 Human_SNP_ID_670934716 A-to-I Human chr19 + 58265461 58265461 58265461 GGGACTACAGGCACCCGTCACCACGTCTGTCTAATTTTTTGTACTTTTAGTAGAGACAAGGTTTC GGGACTACAGGCACCCGTCACCACGTCTGTCTGATTTTTTGTACTTTTAGTAGAGACAAGGTTTC A G ZNF544,AC020915.5 Ensembl:ENSG00000198131,Ensembl:ENSG00000283515 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs988938771 Functional Loss SNV dbSNP153 33..33 33 - - - 15646 RMVar_ID_15646 Human_SNP_ID_670936155 A-to-I Human chr19 + 58269876 58269876 58269876 CTGGGAGGCAGAGGTTGCAATGAGTCTAGATCATGCCACTGGACTCCAGCCTGGGCGACAGAATG CTGGGAGGCAGAGGTTGCAATGAGTCTAGATCGTGCCACTGGACTCCAGCCTGGGCGACAGAATG A G ZNF544,AC020915.5 Ensembl:ENSG00000198131,Ensembl:ENSG00000283515 Protein coding,Protein coding intron,intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1257786768 Functional Loss SNV dbSNP153 33..33 33 - - - 15647 RMVar_ID_15647 Human_SNP_ID_670936581 A-to-I Human chr19 - 58271516 58271516 58271516 CTAACTGCAGCCTCAACCTCCTGGGGTCAAAGAATCCTCCCAACTCAGCTTCCTGAGTAGCTGGG CTAACTGCAGCCTCAACCTCCTGGGGTCAAAGGATCCTCCCAACTCAGCTTCCTGAGTAGCTGGG T C AC020915.3 Ensembl:ENSG00000268516 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs908413474 Functional Loss SNV dbSNP153 33..33 33 - - - 15648 RMVar_ID_15648 Human_SNP_ID_670936673 A-to-I Human chr19 + 58271890 58271890 58271890 TTTAAAAAATCAAGCAAGAGCAGGCTGGGCGCAGTGGCTCATGCCTGTAATCCCAGCACTTTGGG TTTAAAAAATCAAGCAAGAGCAGGCTGGGCGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGG A G ZNF544,AC020915.5 Ensembl:ENSG00000198131,Ensembl:ENSG00000283515 Protein coding,Protein coding intron,intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs576954512 Functional Loss SNV dbSNP153 33..33 33 - - - 15649 RMVar_ID_15649 Human_SNP_ID_670936698 A-to-I Human chr19 + 58271997 58271997 58271997 CAGCCTGGCCGACATGGTGAAACCCTGTCCCCACTAAAAATGCAAAAATTATCTGGGCGTGGTGG CAGCCTGGCCGACATGGTGAAACCCTGTCCCCGCTAAAAATGCAAAAATTATCTGGGCGTGGTGG A G ZNF544,AC020915.5 Ensembl:ENSG00000198131,Ensembl:ENSG00000283515 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1043899720 Functional Loss SNV dbSNP153 33..33 33 - - - 15650 RMVar_ID_15650 Human_SNP_ID_670936788 A-to-I Human chr19 - 58272359 58272359 58272359 CAGAGTCCTGCCATGTTGCCCAGTCTAATCTCAAACTCACGGCCTCAGTTGATCCTTCCACCTGG CAGAGTCCTGCCATGTTGCCCAGTCTAATCTCTAACTCACGGCCTCAGTTGATCCTTCCACCTGG T A AC020915.3 Ensembl:ENSG00000268516 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037585271 Functional Loss SNV dbSNP153 33..33 33 - - - 15651 RMVar_ID_15651 Human_SNP_ID_670937385 A-to-I Human chr19 + 58274030 58274030 58274030 GTTGGCCAGGATGGTCTCGAACTCTTGATCTCATGGTCTGCCCACCTCCGCCTCCCAAAGTGCTG GTTGGCCAGGATGGTCTCGAACTCTTGATCTCGTGGTCTGCCCACCTCCGCCTCCCAAAGTGCTG A G ZNF544,AC020915.5 Ensembl:ENSG00000198131,Ensembl:ENSG00000283515 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1242651705 Functional Loss SNV dbSNP153 33..33 33 - - - 15652 RMVar_ID_15652 Human_SNP_ID_670937388 A-to-I Human chr19 + 58274041 58274041 58274041 TGGTCTCGAACTCTTGATCTCATGGTCTGCCCACCTCCGCCTCCCAAAGTGCTGGGATTACAAGT TGGTCTCGAACTCTTGATCTCATGGTCTGCCCGCCTCCGCCTCCCAAAGTGCTGGGATTACAAGT A G ZNF544,AC020915.5 Ensembl:ENSG00000198131,Ensembl:ENSG00000283515 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1283682737 Functional Loss SNV dbSNP153 33..33 33 - - - 15653 RMVar_ID_15653 Human_SNP_ID_670937398 A-to-I Human chr19 - 58274073 58274073 58274073 AAACTGTTTAGGAGCCGGGCACGGTGGCTCACACTTGTAATCCCAGCACTTTGGGAGGCGGAGGT AAACTGTTTAGGAGCCGGGCACGGTGGCTCACGCTTGTAATCCCAGCACTTTGGGAGGCGGAGGT T C AC020915.3 Ensembl:ENSG00000268516 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006077143 Functional Loss SNV dbSNP153 33..33 33 - - - 15654 RMVar_ID_15654 Human_SNP_ID_670937778 A-to-I Human chr19 - 58275591 58275591 58275591 TTGCCTAGGATGGTCTTGAGCTCCTGATTTCAAGCAGTCCATCCGCCTTGGCCTCCCAAAGTGCT TTGCCTAGGATGGTCTTGAGCTCCTGATTTCACGCAGTCCATCCGCCTTGGCCTCCCAAAGTGCT T G AC020915.3 Ensembl:ENSG00000268516 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1189843902 Functional Loss SNV dbSNP153 33..33 33 - - - 15655 RMVar_ID_15655 Human_SNP_ID_670938397 A-to-I Human chr19 - 58277833 58277833 58277833 TTATTAAAGGTCGGGCGCGGTGGCTAACGCCTATAATCCCAGCACTTTGGGAAGTCGAGGCGGGT TTATTAAAGGTCGGGCGCGGTGGCTAACGCCTGTAATCCCAGCACTTTGGGAAGTCGAGGCGGGT T C AC020915.3 Ensembl:ENSG00000268516 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978938192 Functional Loss SNV dbSNP153 33..33 33 - - - 15656 RMVar_ID_15656 Human_SNP_ID_670943631 A-to-I Human chr19 + 58297066 58297066 58297066 CTAGCCTGGGCCCATGGCGAAACCCCATCTCTACTAAAAATACACAAATTAGCCAAGTGTGGTGA CTAGCCTGGGCCCATGGCGAAACCCCATCTCTTCTAAAAATACACAAATTAGCCAAGTGTGGTGA A T ZNF8,AC020915.5,AC020915.1 Ensembl:ENSG00000278129,Ensembl:ENSG00000283515,Ensembl:ENSG00000267216 Protein coding,Protein coding,lincRNA 3'UTR,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903388573 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124774,RMVar_hsa_circ_196503 15657 RMVar_ID_15657 Human_SNP_ID_670943910 A-to-I Human chr19 + 58298116 58298116 58298116 CAATGGCGTGATCTCGGCTCACTGCAACCTCCACCTCCACGGTTCACGCCATTCTCCTGCCTCAG CAATGGCGTGATCTCGGCTCACTGCAACCTCCGCCTCCACGGTTCACGCCATTCTCCTGCCTCAG A G ZNF8,AC020915.5,AC020915.1 Ensembl:ENSG00000278129,Ensembl:ENSG00000283515,Ensembl:ENSG00000267216 Protein coding,Protein coding,lincRNA 3'UTR,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1224912214 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124774,RMVar_hsa_circ_196503 15658 RMVar_ID_15658 Human_SNP_ID_670944057 A-to-I Human chr19 + 58298577 58298575 58298577 AAACTCATGACCTCAAGTAATCTGCCCGCCTCAGTCTCCCAAAATGCTGGCATTACAGGCATGAG AAACTCATGACCTCAAGTAATCTGCCCGCCT__GTCTCCCAAAATGCTGGCATTACAGGCATGAG TCA T ZNF8,AC020915.5,AC020915.1 Ensembl:ENSG00000278129,Ensembl:ENSG00000283515,Ensembl:ENSG00000267216 Protein coding,Protein coding,lincRNA 3'UTR,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1477848547 Functional Loss DEL dbSNP153 32..33 33 - - - Human_miRNA_ID_2442464,Human_miRNA_ID_3086831 RMVar_hsa_circ_124774,RMVar_hsa_circ_196503 15659 RMVar_ID_15659 Human_SNP_ID_670944191 A-to-I Human chr19 + 58299136 58299136 58299136 TGCCAAACAGCAATTTTTTTTTTTTTTGAGACAGAGTCTCGCTGTGTCACCCAGGCTGGAGTGCA TGCCAAACAGCAATTTTTTTTTTTTTTGAGACGGAGTCTCGCTGTGTCACCCAGGCTGGAGTGCA A G ZNF8,AC020915.5,AC020915.1 Ensembl:ENSG00000278129,Ensembl:ENSG00000283515,Ensembl:ENSG00000267216 Protein coding,Protein coding,lincRNA 3'UTR,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991757634 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124774,RMVar_hsa_circ_196503 15660 RMVar_ID_15660 Human_SNP_ID_670945162 A-to-I Human chr19 + 58303131 58303131 58303131 ATGTTTCCATTTATGTAAAGAAGAAACAGGCTAGGCAAGGTGACTCACGCCTGTAATCCCAGCAC ATGTTTCCATTTATGTAAAGAAGAAACAGGCTGGGCAAGGTGACTCACGCCTGTAATCCCAGCAC A G AC020915.5,AC020915.1 Ensembl:ENSG00000283515,Ensembl:ENSG00000267216 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1568530926 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2402697 RMVar_hsa_circ_124774,RMVar_hsa_circ_196503 15661 RMVar_ID_15661 Human_SNP_ID_670945204 A-to-I Human chr19 + 58303306 58303306 58303306 GCACACTTCTAATCCCAGCTACTCCGTAGGCTAAGGCAGGAGAATCGCTTGAACCCAGGAAGTGG GCACACTTCTAATCCCAGCTACTCCGTAGGCTGAGGCAGGAGAATCGCTTGAACCCAGGAAGTGG A G AC020915.5,AC020915.1 Ensembl:ENSG00000283515,Ensembl:ENSG00000267216 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1568530987 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2743142 RMVar_hsa_circ_124774,RMVar_hsa_circ_196503 15662 RMVar_ID_15662 Human_SNP_ID_670947998 A-to-I Human chr19 + 58314369 58314369 58314369 TCAACCCTGGCCGGGTGCGGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCCGAGGCAGGC TCAACCCTGGCCGGGTGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGC A G ERVK3-1,AC020915.5,AC020915.1 Ensembl:ENSG00000142396,Ensembl:ENSG00000283515,Ensembl:ENSG00000267216 Protein coding,Protein coding,lincRNA intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904197474 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124774,RMVar_hsa_circ_196503 15663 RMVar_ID_15663 Human_SNP_ID_670948034 A-to-I Human chr19 + 58314500 58314500 58314500 TACAAAAAAATTAGCTGGGTGTGGTGGCGGGCACCTGTAGTCCCAGCTAATCAGGAGGCTGAGGT TACAAAAAAATTAGCTGGGTGTGGTGGCGGGCCCCTGTAGTCCCAGCTAATCAGGAGGCTGAGGT A C ERVK3-1,AC020915.5,AC020915.1 Ensembl:ENSG00000142396,Ensembl:ENSG00000283515,Ensembl:ENSG00000267216 Protein coding,Protein coding,lincRNA intron,intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1161662538 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124774,RMVar_hsa_circ_196503 15664 RMVar_ID_15664 Human_SNP_ID_670951896 A-to-I Human chr19 + 58330100 58330100 58330100 CATGAGGTCAGGAGATCGAGACCATCGTGGCTAATACGGTGAAACCCCGTCTCTACTAAAAGTAC CATGAGGTCAGGAGATCGAGACCATCGTGGCTTATACGGTGAAACCCCGTCTCTACTAAAAGTAC A T ZSCAN22 Ensembl:ENSG00000182318 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1479285072 Functional Loss SNV dbSNP153 33..33 33 - - - 15665 RMVar_ID_15665 Human_SNP_ID_670958786 A-to-I Human chr19 + 58353725 58353725 58353725 ACCACCTCATCCTCATTTCAGTGATGGATCCTAGAACCTGTTCTAGAAGGAGACGCTGAGTTCTC ACCACCTCATCCTCATTTCAGTGATGGATCCTGGAACCTGTTCTAGAAGGAGACGCTGAGTTCTC A G A1BG-AS1 Ensembl:ENSG00000268895 lincRNA exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs893180 Functional Loss SNV dbSNP153,JSNP 33..33 33 - - - Human_RBP_ID_5587297 Human_Splice_Rec_2051762,Human_Splice_Rec_2051766,Human_Splice_Rec_2051770,Human_Splice_Rec_2051774,Human_Splice_Rec_2051778,Human_Splice_Rec_2051782,Human_Splice_Rec_2051786,Human_Splice_Rec_2051790,Human_Splice_Rec_2051794 15666 RMVar_ID_15666 Human_SNP_ID_670961256 A-to-I Human chr19 - 58359717 58359717 58359717 CACCCACCTCGGCCTCCCAAAGTGCTAGGACTACAGCCGTCAGCCACCGCACTTGGCCTAACTTA CACCCACCTCGGCCTCCCAAAGTGCTAGGACTGCAGCCGTCAGCCACCGCACTTGGCCTAACTTA T C AC012313.3,ZNF497 Ensembl:ENSG00000268230,Ensembl:ENSG00000174586 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1291463817 Functional Loss SNV dbSNP153 33..33 33 - - - 15667 RMVar_ID_15667 Human_SNP_ID_670961257 A-to-I Human chr19 - 58359723 58359723 58359723 GTGATCCACCCACCTCGGCCTCCCAAAGTGCTAGGACTACAGCCGTCAGCCACCGCACTTGGCCT GTGATCCACCCACCTCGGCCTCCCAAAGTGCTGGGACTACAGCCGTCAGCCACCGCACTTGGCCT T C AC012313.3,ZNF497 Ensembl:ENSG00000268230,Ensembl:ENSG00000174586 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs112950091 Functional Loss SNV dbSNP153 33..33 33 - - - 15668 RMVar_ID_15668 Human_SNP_ID_670961260 A-to-I Human chr19 - 58359730 58359728 58359730 TGACCTCGTGATCCACCCACCTCGGCCTCCCAAAGTGCTAGGACTACAGCCGTCAGCCACCGCAC TGACCTCGTGATCCACCCACCTCGGCCTCCCA__GTGCTAGGACTACAGCCGTCAGCCACCGCAC CTT C AC012313.3,ZNF497 Ensembl:ENSG00000268230,Ensembl:ENSG00000174586 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1158322353 Functional Loss DEL dbSNP153 33..34 33 - - - 15669 RMVar_ID_15669 Human_SNP_ID_670961275 A-to-I Human chr19 - 58359790 58359790 58359790 TTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGGTCTTGGAATTGCTGACC TTTTGTATTTTTAGTAGAGACGGGGTTTCACCGTGTTGGCCAGGCTGGTCTTGGAATTGCTGACC T C AC012313.3,ZNF497 Ensembl:ENSG00000268230,Ensembl:ENSG00000174586 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1311110969 Functional Loss SNV dbSNP153 33..33 33 - - - 15670 RMVar_ID_15670 Human_SNP_ID_670961593 A-to-I Human chr19 - 58360745 58360739 58360746 AAAAAAAAAAGAGTTCGGGACCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAAATAA AAAAAAAAAAGAGTTCGGGACCAGCCTGGCC_______TGAAACCCCATCTCTACTAAAAAATAA ACCATGTT A AC012313.3,ZNF497 Ensembl:ENSG00000268230,Ensembl:ENSG00000174586 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs891968189 Functional Loss DEL dbSNP153 32..38 33 - - - 15671 RMVar_ID_15671 Human_SNP_ID_670961943 A-to-I Human chr19 + 58361631 58361630 58361632 CACCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGACATGAGCCACCGCACCTGGCCTCTAGTT CACCCGCCTTGGCCTCCCAAAGTGCTGGGATT__AGACATGAGCCACCGCACCTGGCCTCTAGTT TAC T - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs773680598 Functional Loss DEL dbSNP153 33..34 33 - - - 15672 RMVar_ID_15672 Human_SNP_ID_670969315 A-to-I Human chr19 + 58384468 58384468 58384468 AGGAGCTATCACGGCCAGGTGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGC AGGAGCTATCACGGCCAGGTGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335369822 Functional Loss SNV dbSNP153 33..33 33 - - - 15673 RMVar_ID_15673 Human_SNP_ID_670970750 A-to-I Human chr19 + 58388764 58388764 58388764 CTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGTGCCCGCCACTGCACCTGGCTGATTTTT CTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTGCAGGTGCCCGCCACTGCACCTGGCTGATTTTT A G RPS5 Ensembl:ENSG00000083845 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs963439747 Functional Loss SNV dbSNP153 33..33 33 - - - 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 15674 RMVar_ID_15674 Human_SNP_ID_670971349 A-to-I Human chr19 + 58390625 58390624 58390626 ACCTGGCTAATTTTTGTCTTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGCCTTGA ACCTGGCTAATTTTTGTCTTTTTAGTAGAGAC__GGTTTCACCATGTTGGCCAGGCTGGCCTTGA CAG C RPS5 Ensembl:ENSG00000083845 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs918649930 Functional Loss DEL dbSNP153 33..34 33 - - - 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 15675 RMVar_ID_15675 Human_SNP_ID_670971350 A-to-I Human chr19 + 58390625 58390625 58390625 ACCTGGCTAATTTTTGTCTTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGCCTTGA ACCTGGCTAATTTTTGTCTTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGGCCTTGA A G RPS5 Ensembl:ENSG00000083845 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1345399059 Functional Loss SNV dbSNP153 33..33 33 - - - 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 15676 RMVar_ID_15676 Human_SNP_ID_670971535 A-to-I Human chr19 + 58391338 58391337 58391338 CCTGTTGTCCCAGCTACTTAGGAGGCTGATGCAGGAGAATCGCTTGAACCTGGGAGGTGGAGGTT CCTGTTGTCCCAGCTACTTAGGAGGCTGATGC_GGAGAATCGCTTGAACCTGGGAGGTGGAGGTT CA C RPS5 Ensembl:ENSG00000083845 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1189160790 Functional Loss DEL dbSNP153 33..33 33 - - - 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 15677 RMVar_ID_15677 Human_SNP_ID_670971672 A-to-I Human chr19 + 58391716 58391716 58391716 GGGAGGCTGAGGCGGACGGATCACCTGAGGTCAAGAGTTCAAGACCAGCCTGGCCAACATGTCCA GGGAGGCTGAGGCGGACGGATCACCTGAGGTCGAGAGTTCAAGACCAGCCTGGCCAACATGTCCA A G RPS5 Ensembl:ENSG00000083845 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs953334341 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18741339 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 15678 RMVar_ID_15678 Human_SNP_ID_670971688 A-to-I Human chr19 + 58391795 58391795 58391795 TAAAAATACAAAAATTAGCCTGGCATGGTGGCATGCACCTGTAGTCCCAGCTACTCAGGAAGCTG TAAAAATACAAAAATTAGCCTGGCATGGTGGCGTGCACCTGTAGTCCCAGCTACTCAGGAAGCTG A G RPS5 Ensembl:ENSG00000083845 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1379101659 Functional Loss SNV dbSNP153 33..33 33 - - - 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 15679 RMVar_ID_15679 Human_SNP_ID_670971691 A-to-I Human chr19 + 58391805 58391805 58391805 AAAATTAGCCTGGCATGGTGGCATGCACCTGTAGTCCCAGCTACTCAGGAAGCTGAGGCAGGAGA AAAATTAGCCTGGCATGGTGGCATGCACCTGTCGTCCCAGCTACTCAGGAAGCTGAGGCAGGAGA A C RPS5 Ensembl:ENSG00000083845 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1267594528 Functional Loss SNV dbSNP153 33..33 33 - - - 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 15680 RMVar_ID_15680 Human_SNP_ID_670971919 A-to-I Human chr19 + 58392502 58392502 58392502 AAAAAACTAGCTAGGCTTGGTGGCAGGCCCCTATAATCCTAGCTACTCGGGAGGTTGAGGCAGGA AAAAAACTAGCTAGGCTTGGTGGCAGGCCCCTGTAATCCTAGCTACTCGGGAGGTTGAGGCAGGA A G RPS5 Ensembl:ENSG00000083845 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs541053215 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22741895 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 15681 RMVar_ID_15681 Human_SNP_ID_670971920 A-to-I Human chr19 + 58392504 58392504 58392504 AAAACTAGCTAGGCTTGGTGGCAGGCCCCTATAATCCTAGCTACTCGGGAGGTTGAGGCAGGAGA AAAACTAGCTAGGCTTGGTGGCAGGCCCCTATCATCCTAGCTACTCGGGAGGTTGAGGCAGGAGA A C RPS5 Ensembl:ENSG00000083845 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1232006856 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9928815,Human_RBP_ID_22741895 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 15682 RMVar_ID_15682 Human_SNP_ID_670971921 A-to-I Human chr19 + 58392504 58392504 58392504 AAAACTAGCTAGGCTTGGTGGCAGGCCCCTATAATCCTAGCTACTCGGGAGGTTGAGGCAGGAGA AAAACTAGCTAGGCTTGGTGGCAGGCCCCTATGATCCTAGCTACTCGGGAGGTTGAGGCAGGAGA A G RPS5 Ensembl:ENSG00000083845 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1232006856 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9928815,Human_RBP_ID_22741895 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 15683 RMVar_ID_15683 Human_SNP_ID_670981573 A-to-I Human chr19 + 58420298 58420298 58420298 AAAATTAGCCCGGCATGGTGACGGGCGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA AAAATTAGCCCGGCATGGTGACGGGCGCCTGTTGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA A T - - Other Unknown GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1172726997 Functional Loss SNV dbSNP153 33..33 33 - - - 15684 RMVar_ID_15684 Human_SNP_ID_670981675 A-to-I Human chr19 + 58420719 58420719 58420719 TTCCTGGCTTATACCCACTTTTATTTTATTTTATTTTTTTTGAGATGGAGTCACTCTGTTGTCCA TTCCTGGCTTATACCCACTTTTATTTTATTTTTTTTTTTTTGAGATGGAGTCACTCTGTTGTCCA A T - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1174893396 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6791976,Human_RBP_ID_17933178,Human_RBP_ID_23181072 15685 RMVar_ID_15685 Human_SNP_ID_670981746 A-to-I Human chr19 + 58420956 58420956 58420956 TCGAACTCCTGACCTTGTGATCTGCCCACCTCAGCCTTTCAAAGTGCTGGGATTACCGGCGTGAG TCGAACTCCTGACCTTGTGATCTGCCCACCTCGGCCTTTCAAAGTGCTGGGATTACCGGCGTGAG A G - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1460585812 Functional Loss SNV dbSNP153 33..33 33 - - - 15686 RMVar_ID_15686 Human_SNP_ID_670982189 A-to-I Human chr19 + 58422893 58422892 58422894 ATATTTTGTTTTGTTTTTGTTTGTTTTGAGACAGAGTCTCGCTCTGTTGCCCAGGCTGGAGTGCA ATATTTTGTTTTGTTTTTGTTTGTTTTGAGAC__AGTCTCGCTCTGTTGCCCAGGCTGGAGTGCA CAG C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1271547182 Functional Loss DEL dbSNP153 33..34 33 - - - 15687 RMVar_ID_15687 Human_SNP_ID_670982551 A-to-I Human chr19 + 58424128 58424128 58424128 AAAATTAGCCAGGTGTGGTGGCGCATGGCTGTAATCTCAGCTACTTGGGAGGCTAAGGCAGGAGA AAAATTAGCCAGGTGTGGTGGCGCATGGCTGTCATCTCAGCTACTTGGGAGGCTAAGGCAGGAGA A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1568592777 Functional Loss SNV dbSNP153 33..33 33 - - - 15688 RMVar_ID_15688 Human_SNP_ID_670984382 A-to-I Human chr19 + 58429467 58429467 58429467 GGCTCACTGCACACCCTGCCTCCCAGGTTCACACCATTCTCCTGCCTCAGCCTCCTAAGTAGCTG GGCTCACTGCACACCCTGCCTCCCAGGTTCACGCCATTCTCCTGCCTCAGCCTCCTAAGTAGCTG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1169948241 Functional Loss SNV dbSNP153 33..33 33 - - - 15689 RMVar_ID_15689 Human_SNP_ID_670993138 A-to-I Human chr19 + 58458615 58458602 58458616 TATTAGTCTGTTTTGTGTCACTATAAAGGAACACCTAAGGCTGGGTAATTTATAAAGAAAAGAGG TATTAGTCTGTTTTGTGTCA______________CTAAGGCTGGGTAATTTATAAAGAAAAGAGG ACTATAAAGGAACAC A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1284126599 Functional Loss DEL dbSNP153 21..34 33 - - - Human_RBP_ID_13526838 15690 RMVar_ID_15690 Human_SNP_ID_671004056 A-to-I Human chr19 + 58490241 58490241 58490241 AAAGCTCTCAGATTATAGGCATGAGCCACCATACCTGGCCCCATAGTTGAACTTAAAATAGACTA AAAGCTCTCAGATTATAGGCATGAGCCACCATGCCTGGCCCCATAGTTGAACTTAAAATAGACTA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1490312233 Functional Loss SNV dbSNP153 33..33 33 - - - 15691 RMVar_ID_15691 Human_SNP_ID_671004732 A-to-I Human chr19 - 58492613 58492613 58492613 TTTAGTACAGACGAGGTTTCACCGTGTTACCCAGGATGGTCTCGATCTCTTGACCTCGTGATCCG TTTAGTACAGACGAGGTTTCACCGTGTTACCCCGGATGGTCTCGATCTCTTGACCTCGTGATCCG T G SLC27A5 Ensembl:ENSG00000083807 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934776709 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122226,RMVar_hsa_circ_196534 15692 RMVar_ID_15692 Human_SNP_ID_671029737 A-to-I Human chr19 - 58565156 58565156 58565156 CAGGAGATGGAGGTTTGCAGTGAGCAGAGAACACGCCATTGCACTCCAACCTGGGCAACAAGAGC CAGGAGATGGAGGTTTGCAGTGAGCAGAGAACCCGCCATTGCACTCCAACCTGGGCAACAAGAGC T G MZF1 Ensembl:ENSG00000099326 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs529218175 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9928882,Human_RBP_ID_13527816,Human_RBP_ID_25437659 RMVar_hsa_circ_113163,RMVar_hsa_circ_196586 15693 RMVar_ID_15693 Human_SNP_ID_671029841 A-to-I Human chr19 - 58565509 58565509 58565509 CACACACACACGGGCTGGGCGTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAAGGCGAGGC CACACACACACGGGCTGGGCGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAAGGCGAGGC T C MZF1 Ensembl:ENSG00000099326 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1248502362 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113163,RMVar_hsa_circ_196586 15694 RMVar_ID_15694 Human_SNP_ID_671030103 A-to-I Human chr19 - 58566019 58566019 58566019 CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCGGCCACCACGCCTGGCTAAATATT CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTTCAGGCGCCGGCCACCACGCCTGGCTAAATATT T A MZF1 Ensembl:ENSG00000099326 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs763931377 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113163,RMVar_hsa_circ_196586 15695 RMVar_ID_15695 Human_SNP_ID_671030681 A-to-I Human chr19 - 58568019 58568019 58568019 TTGCCAGGGCTGGTCTTAAATTCCTGGCTTCAAGTGATGCTCCCACCTCAGCCTCCCAGAGTGCT TTGCCAGGGCTGGTCTTAAATTCCTGGCTTCAGGTGATGCTCCCACCTCAGCCTCCCAGAGTGCT T C MZF1 Ensembl:ENSG00000099326 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs575758092 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113163,RMVar_hsa_circ_196586 15696 RMVar_ID_15696 Human_SNP_ID_671030698 A-to-I Human chr19 - 58568117 58568117 58568117 CCTCAGCCTCCCAAGTATCTGGGACTGCAGGCATGTGTCACTGTACCTGACTCATTTTTAATTTT CCTCAGCCTCCCAAGTATCTGGGACTGCAGGCGTGTGTCACTGTACCTGACTCATTTTTAATTTT T C MZF1 Ensembl:ENSG00000099326 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1203461314 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8496104,Human_RBP_ID_13527953 RMVar_hsa_circ_113163,RMVar_hsa_circ_196586 15697 RMVar_ID_15697 Human_SNP_ID_671030702 A-to-I Human chr19 - 58568133 58568133 58568133 TCAAGTGATCCTCTCGCCTCAGCCTCCCAAGTATCTGGGACTGCAGGCATGTGTCACTGTACCTG TCAAGTGATCCTCTCGCCTCAGCCTCCCAAGTGTCTGGGACTGCAGGCATGTGTCACTGTACCTG T C MZF1 Ensembl:ENSG00000099326 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560512479 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13527953 RMVar_hsa_circ_113163,RMVar_hsa_circ_196586 15698 RMVar_ID_15698 Human_SNP_ID_671030704 A-to-I Human chr19 - 58568136 58568136 58568136 GGCTCAAGTGATCCTCTCGCCTCAGCCTCCCAAGTATCTGGGACTGCAGGCATGTGTCACTGTAC GGCTCAAGTGATCCTCTCGCCTCAGCCTCCCAGGTATCTGGGACTGCAGGCATGTGTCACTGTAC T C MZF1 Ensembl:ENSG00000099326 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs376036577 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113163,RMVar_hsa_circ_196586 15699 RMVar_ID_15699 Human_SNP_ID_671030710 A-to-I Human chr19 - 58568163 58568163 58568163 ATAGCTTACTGTAACCTTGAACTCCTGGGCTCAAGTGATCCTCTCGCCTCAGCCTCCCAAGTATC ATAGCTTACTGTAACCTTGAACTCCTGGGCTCCAGTGATCCTCTCGCCTCAGCCTCCCAAGTATC T G MZF1 Ensembl:ENSG00000099326 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs775311253 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13527966 RMVar_hsa_circ_113163,RMVar_hsa_circ_196586 15700 RMVar_ID_15700 Human_SNP_ID_671030723 A-to-I Human chr19 - 58568214 58568214 58568214 GGGGGAGGGGGTCTCACTATTTCACACAGACTAGAGCACAGTGGTGCCATCATAGCTTACTGTAA GGGGGAGGGGGTCTCACTATTTCACACAGACTGGAGCACAGTGGTGCCATCATAGCTTACTGTAA T C MZF1 Ensembl:ENSG00000099326 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs183783635 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9928900,Human_RBP_ID_13527966,Human_RBP_ID_20425772,Human_RBP_ID_23232224,Human_RBP_ID_25448499,Human_RBP_ID_26996942 RMVar_hsa_circ_113163,RMVar_hsa_circ_196586 15701 RMVar_ID_15701 Human_SNP_ID_671032796 A-to-I Human chr19 + 58574570 58574570 58574570 CGAGTAGCTGGGACTGCAGGCTGCTCCACCACACCCGGCTGATTTTTGTATTTTTAGTAGAGATG CGAGTAGCTGGGACTGCAGGCTGCTCCACCACGCCCGGCTGATTTTTGTATTTTTAGTAGAGATG A G MZF1-AS1,CENPBD1P1 Ensembl:ENSG00000267858,Ensembl:ENSG00000213753 lincRNA,Pseudogene exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893025486 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_139143,Human_RBP_ID_528630,Human_RBP_ID_6792322,Human_RBP_ID_8256457,Human_RBP_ID_13528147 15702 RMVar_ID_15702 Human_SNP_ID_671035555 A-to-I Human chr19 + 58584082 58584082 58584082 ACACCACCTTTGGGGTGGCTGCATTGGCTCACACCTGTAATCTCAGCACTTTAGGAGGCTGAGGC ACACCACCTTTGGGGTGGCTGCATTGGCTCACGCCTGTAATCTCAGCACTTTAGGAGGCTGAGGC A G CENPBD1P1,AC016629.3 Ensembl:ENSG00000213753,Ensembl:ENSG00000286104 Pseudogene,lincRNA intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1053890 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17387616 RMVar_hsa_circ_79274,RMVar_hsa_circ_196588 15703 RMVar_ID_15703 Human_SNP_ID_671035559 A-to-I Human chr19 + 58584102 58584102 58584102 GCATTGGCTCACACCTGTAATCTCAGCACTTTAGGAGGCTGAGGCAGGAGGATAGCTTGAGGCCA GCATTGGCTCACACCTGTAATCTCAGCACTTTGGGAGGCTGAGGCAGGAGGATAGCTTGAGGCCA A G CENPBD1P1,AC016629.3 Ensembl:ENSG00000213753,Ensembl:ENSG00000286104 Pseudogene,lincRNA intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1133047 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17387616 RMVar_hsa_circ_79274,RMVar_hsa_circ_196588 15704 RMVar_ID_15704 Human_SNP_ID_671035563 A-to-I Human chr19 + 58584115 58584115 58584115 CCTGTAATCTCAGCACTTTAGGAGGCTGAGGCAGGAGGATAGCTTGAGGCCAGGAGTTCGAGACT CCTGTAATCTCAGCACTTTAGGAGGCTGAGGCGGGAGGATAGCTTGAGGCCAGGAGTTCGAGACT A G CENPBD1P1,AC016629.3 Ensembl:ENSG00000213753,Ensembl:ENSG00000286104 Pseudogene,lincRNA intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-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 15705 RMVar_ID_15705 Human_SNP_ID_671035574 A-to-I Human chr19 + 58584157 58584157 58584157 CTTGAGGCCAGGAGTTCGAGACTAACCGGAGCAACATAGTAAGGCCACATCTGTACAAAAAAAAG CTTGAGGCCAGGAGTTCGAGACTAACCGGAGCGACATAGTAAGGCCACATCTGTACAAAAAAAAG A G CENPBD1P1,AC016629.3 Ensembl:ENSG00000213753,Ensembl:ENSG00000286104 Pseudogene,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1217416533 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13528227 RMVar_hsa_circ_79274,RMVar_hsa_circ_196588 15706 RMVar_ID_15706 Human_SNP_ID_671035575 A-to-I Human chr19 + 58584165 58584161 58584165 CAGGAGTTCGAGACTAACCGGAGCAACATAGTAAGGCCACATCTGTACAAAAAAAAGAAAGAAAA CAGGAGTTCGAGACTAACCGGAGCAACAT____AGGCCACATCTGTACAAAAAAAAGAAAGAAAA TAGTA T CENPBD1P1,AC016629.3 Ensembl:ENSG00000213753,Ensembl:ENSG00000286104 Pseudogene,lincRNA intron,intron GSE38233;GSE100210;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,frontal_cortex - 24183664,29129909,30559470 RNA-Seq:(High) rs1229331931 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_13528227,Human_RBP_ID_20433581 RMVar_hsa_circ_79274,RMVar_hsa_circ_196588 15707 RMVar_ID_15707 Human_SNP_ID_671035576 A-to-I Human chr19 + 58584165 58584165 58584165 CAGGAGTTCGAGACTAACCGGAGCAACATAGTAAGGCCACATCTGTACAAAAAAAAGAAAGAAAA CAGGAGTTCGAGACTAACCGGAGCAACATAGTGAGGCCACATCTGTACAAAAAAAAGAAAGAAAA A G CENPBD1P1,AC016629.3 Ensembl:ENSG00000213753,Ensembl:ENSG00000286104 Pseudogene,lincRNA intron,intron GSE38233;GSE100210;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,frontal_cortex - 24183664,29129909,30559470 RNA-Seq:(High) rs1290599545 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13528227,Human_RBP_ID_20433581 RMVar_hsa_circ_79274,RMVar_hsa_circ_196588 15708 RMVar_ID_15708 Human_SNP_ID_26315181 A-to-I Human chr1 + 105434593 105434593 105434593 TTCCTCAAAAGCCTCTCTTCTGTGGAAGCTCTAAAGCCAACTAGTTGGGCAAAATCTTTAACCTG TTCCTCAAAAGCCTCTCTTCTGTGGAAGCTCTGAAGCCAACTAGTTGGGCAAAATCTTTAACCTG A G CDK4P1 Ensembl:ENSG00000225036 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1055694347 Functional Loss SNV dbSNP153 33..33 33 - - - 15709 RMVar_ID_15709 Human_SNP_ID_26443435 A-to-I Human chr1 + 105892845 105892845 105892845 CTGGGATCTCCACCTCCCTCGTTTCATCTTGGAGGACCAGCAATTGGACCAAGAGGAAATCTGGG CTGGGATCTCCACCTCCCTCGTTTCATCTTGGGGGACCAGCAATTGGACCAAGAGGAAATCTGGG A G AL512844.1 Ensembl:ENSG00000232952 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878896457 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1407323,Human_RBP_ID_1721173,Human_RBP_ID_18509737,Human_RBP_ID_18546427 Human_miRNA_ID_1825496,Human_miRNA_ID_1825659 15710 RMVar_ID_15710 Human_SNP_ID_27022985 A-to-I Human chr1 - 108193360 108193360 108193360 AATGGGGCATAAAGATGGGAACAATAGACACTAGGGACTCCAAAAGGGGGGAGGGAGGGAGGAGG AATGGGGCATAAAGATGGGAACAATAGACACTGGGGACTCCAAAAGGGGGGAGGGAGGGAGGAGG T C SLC25A24 Ensembl:ENSG00000085491 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1224458278 Functional Loss SNV dbSNP153 33..33 33 - - - 15711 RMVar_ID_15711 Human_SNP_ID_27022986 A-to-I Human chr1 - 108193360 108193360 108193360 AATGGGGCATAAAGATGGGAACAATAGACACTAGGGACTCCAAAAGGGGGGAGGGAGGGAGGAGG AATGGGGCATAAAGATGGGAACAATAGACACTCGGGACTCCAAAAGGGGGGAGGGAGGGAGGAGG T G SLC25A24 Ensembl:ENSG00000085491 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1224458278 Functional Loss SNV dbSNP153 33..33 33 - - - 15712 RMVar_ID_15712 Human_SNP_ID_27097655 A-to-I Human chr1 + 108623691 108623691 108623691 ATCTACAAAAATAAAAAAATATTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCAGGCTGGAG ATCTACAAAAATAAAAAAATATTTTTTTTTTGCGACGGAGTCTCGCTCTGTCGCCCAGGCTGGAG A C FAM102B Ensembl:ENSG00000162636 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1179376296 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50206,RMVar_hsa_circ_330946,RMVar_hsa_circ_356091 15713 RMVar_ID_15713 Human_SNP_ID_27104870 A-to-I Human chr1 - 108652758 108652758 108652758 TTGTATTTTTAGTAGAGATGGGGTTTCACCCTATTGGCCAGGCTGGTCTTGAACCCCTGACCTCG TTGTATTTTTAGTAGAGATGGGGTTTCACCCTGTTGGCCAGGCTGGTCTTGAACCCCTGACCTCG T C HENMT1 Ensembl:ENSG00000162639 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025691397 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_135045,RMVar_hsa_circ_276521,RMVar_hsa_circ_335478,RMVar_hsa_circ_349027,RMVar_hsa_circ_39613,RMVar_hsa_circ_135049,RMVar_hsa_circ_135050,RMVar_hsa_circ_135048 15714 RMVar_ID_15714 Human_SNP_ID_27139634 A-to-I Human chr1 + 108787994 108787994 108787994 GTGTGTTTTTAATAGAGACAGAATTTCACCATATTGCTCAGGCTGGTCTCGAACTCCTGAGCTCA GTGTGTTTTTAATAGAGACAGAATTTCACCATGTTGCTCAGGCTGGTCTCGAACTCCTGAGCTCA A G STXBP3 Ensembl:ENSG00000116266 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1309204776 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_62063,RMVar_hsa_circ_47871,RMVar_hsa_circ_55000,RMVar_hsa_circ_47496,RMVar_hsa_circ_301739,RMVar_hsa_circ_56934,RMVar_hsa_circ_55806,RMVar_hsa_circ_312169,RMVar_hsa_circ_364248,RMVar_hsa_circ_281894,RMVar_hsa_circ_58887,RMVar_hsa_circ_135060,RMVar_hsa_circ_54901 15715 RMVar_ID_15715 Human_SNP_ID_27144087 A-to-I Human chr1 + 108807207 108807207 108807207 TGTGACCCAGGAGGCGGAGGTTGCAGTGAACCAAGATCGCTCCACTGCAGTCCAGCCTGGGCTAC TGTGACCCAGGAGGCGGAGGTTGCAGTGAACCGAGATCGCTCCACTGCAGTCCAGCCTGGGCTAC A G STXBP3 Ensembl:ENSG00000116266 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1436495956 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_364248,RMVar_hsa_circ_354408,RMVar_hsa_circ_267176,RMVar_hsa_circ_69760,RMVar_hsa_circ_347424 15716 RMVar_ID_15716 Human_SNP_ID_27162450 A-to-I Human chr1 + 108882029 108882029 108882029 ACTGGAGTGCAGTGGTGCAATCATCGATTACTATAACCTCCAACTCCTGGGCTCAAGCAATCCTC ACTGGAGTGCAGTGGTGCAATCATCGATTACTGTAACCTCCAACTCCTGGGCTCAAGCAATCCTC A G GPSM2 Ensembl:ENSG00000121957 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042672065 Functional Loss SNV dbSNP153 33..33 33 - - - 15717 RMVar_ID_15717 Human_SNP_ID_27168923 A-to-I Human chr1 - 108911470 108911470 108911470 CAGGCTAGAGTGCAGTGGCGTGATCTCGGCTCACTGCAACCTCCACCTCCTGGGTTCAAGACATT CAGGCTAGAGTGCAGTGGCGTGATCTCGGCTCGCTGCAACCTCCACCTCCTGGGTTCAAGACATT T C AKNAD1 Ensembl:ENSG00000162641 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1183618670 Functional Loss SNV dbSNP153 33..33 33 - - - 15718 RMVar_ID_15718 Human_SNP_ID_27172061 A-to-I Human chr1 - 108923285 108923285 108923285 TCATGCCTGGAATACCAGCACTTTGGGAGGCTAAGGCAGGAGGATCACTTGAGGCCAGGAGCTCA TCATGCCTGGAATACCAGCACTTTGGGAGGCTGAGGCAGGAGGATCACTTGAGGCCAGGAGCTCA T C AKNAD1 Ensembl:ENSG00000162641 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270115068 Functional Loss SNV dbSNP153 33..33 33 - - - 15719 RMVar_ID_15719 Human_SNP_ID_27173644 A-to-I Human chr1 + 108929872 108929872 108929872 GAGATCAAAACAGAGACACTGACTTTGGGCTAAAGGACTTTTTGCAAAATAATGCTTTGTTGGAG GAGATCAAAACAGAGACACTGACTTTGGGCTATAGGACTTTTTGCAAAATAATGCTTTGTTGGAG A T GPSM2 Ensembl:ENSG00000121957 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1183342637 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_319910,Human_RBP_ID_3275449,Human_RBP_ID_8280010,Human_RBP_ID_8732039 Human_miRNA_ID_1308360,Human_miRNA_ID_2643979,Human_miRNA_ID_2643980 RMVar_hsa_circ_110320,RMVar_hsa_circ_310264,RMVar_hsa_circ_135068,RMVar_hsa_circ_135076,RMVar_hsa_circ_135077,RMVar_hsa_circ_342300,RMVar_hsa_circ_135082,RMVar_hsa_circ_75611,RMVar_hsa_circ_28483,RMVar_hsa_circ_311947,RMVar_hsa_circ_135087,RMVar_hsa_circ_122592,RMVar_hsa_circ_135088,RMVar_hsa_circ_296427,RMVar_hsa_circ_135089,RMVar_hsa_circ_135090 15720 RMVar_ID_15720 Human_SNP_ID_27174255 A-to-I Human chr1 + 108932001 108932001 108932001 CCTAAAAGCTTCACACTATATAGGCTGGGCACAATGGCTCATGCCTGTAATCCCAGCACTTTGGG CCTAAAAGCTTCACACTATATAGGCTGGGCACGATGGCTCATGCCTGTAATCCCAGCACTTTGGG A G GPSM2 Ensembl:ENSG00000121957 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs945361550 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110320,RMVar_hsa_circ_135077,RMVar_hsa_circ_135082,RMVar_hsa_circ_75611,RMVar_hsa_circ_122592,RMVar_hsa_circ_135090 15721 RMVar_ID_15721 Human_SNP_ID_27174325 A-to-I Human chr1 - 108932268 108932268 108932268 GTGAAGCTTTTTTGAAATTTTACTTTTTTTTGAGAGTTTTGCTCTGTCACCCAGGCTGGAGTGAG GTGAAGCTTTTTTGAAATTTTACTTTTTTTTGGGAGTTTTGCTCTGTCACCCAGGCTGGAGTGAG T C CLCC1,AKNAD1 Ensembl:ENSG00000121940,Ensembl:ENSG00000162641 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1263142864 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2083180,Human_RBP_ID_5665571,Human_RBP_ID_10504537 Human_miRNA_ID_1098663,Human_miRNA_ID_1526857 15722 RMVar_ID_15722 Human_SNP_ID_27175104 A-to-I Human chr1 - 108935608 108935608 108935608 GCATATACGACCATGCCTGGCTAATATTTTTTATTTTTTGTGGATATGGGGTCTTGCTGTTACCC GCATATACGACCATGCCTGGCTAATATTTTTTTTTTTTTGTGGATATGGGGTCTTGCTGTTACCC T A CLCC1,AKNAD1 Ensembl:ENSG00000121940,Ensembl:ENSG00000162641 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1161760587 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76209,RMVar_hsa_circ_53675,RMVar_hsa_circ_135091 15723 RMVar_ID_15723 Human_SNP_ID_27175105 A-to-I Human chr1 - 108935617 108935617 108935617 GGACTATAGGCATATACGACCATGCCTGGCTAATATTTTTTATTTTTTGTGGATATGGGGTCTTG GGACTATAGGCATATACGACCATGCCTGGCTAGTATTTTTTATTTTTTGTGGATATGGGGTCTTG T C CLCC1,AKNAD1 Ensembl:ENSG00000121940,Ensembl:ENSG00000162641 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1052396090 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76209,RMVar_hsa_circ_53675,RMVar_hsa_circ_135091 15724 RMVar_ID_15724 Human_SNP_ID_27175277 A-to-I Human chr1 + 108936157 108936124 108936158 CTCTGTCACCCAGGCTGGAGTGCAATGGCACGATCTCGGCTCACTGCAACCTCCGCCCCCTGGAA __________________________________CTCGGCTCACTGCAACCTCCGCCCCCTGGAA ACTCTGTCACCCAGGCTGGAGTGCAATGGCACGAT A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1451722975 Functional Loss DEL dbSNP153 1..34 33 - - - 15725 RMVar_ID_15725 Human_SNP_ID_27175285 A-to-I Human chr1 + 108936157 108936154 108936158 CTCTGTCACCCAGGCTGGAGTGCAATGGCACGATCTCGGCTCACTGCAACCTCCGCCCCCTGGAA CTCTGTCACCCAGGCTGGAGTGCAATGGCA____CTCGGCTCACTGCAACCTCCGCCCCCTGGAA ACGAT A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1380005369 Functional Loss DEL dbSNP153 31..34 33 - - - 15726 RMVar_ID_15726 Human_SNP_ID_27175288 A-to-I Human chr1 + 108936157 108936157 108936157 CTCTGTCACCCAGGCTGGAGTGCAATGGCACGATCTCGGCTCACTGCAACCTCCGCCCCCTGGAA CTCTGTCACCCAGGCTGGAGTGCAATGGCACGGTCTCGGCTCACTGCAACCTCCGCCCCCTGGAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs939554268 Functional Loss SNV dbSNP153 33..33 33 - - - 15727 RMVar_ID_15727 Human_SNP_ID_27177396 A-to-I Human chr1 - 108944407 108944407 108944407 TGGAGTGCAGTGGTATGCTCATAGCTTACTGCAGCCTCGAATCCGGGGCACAGACAATTCTTCTG TGGAGTGCAGTGGTATGCTCATAGCTTACTGCGGCCTCGAATCCGGGGCACAGACAATTCTTCTG T C CLCC1,AKNAD1 Ensembl:ENSG00000121940,Ensembl:ENSG00000162641 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1012073977 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28139,RMVar_hsa_circ_53675,RMVar_hsa_circ_305025,RMVar_hsa_circ_135098,RMVar_hsa_circ_291833,RMVar_hsa_circ_61756,RMVar_hsa_circ_135099,RMVar_hsa_circ_363486 15728 RMVar_ID_15728 Human_SNP_ID_27177563 A-to-I Human chr1 - 108944918 108944918 108944918 TTATAGAAGATAACTACTGTGAGGCCGGGTGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGG TTATAGAAGATAACTACTGTGAGGCCGGGTGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG T C CLCC1,AKNAD1 Ensembl:ENSG00000121940,Ensembl:ENSG00000162641 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs538936792 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28139,RMVar_hsa_circ_53675,RMVar_hsa_circ_305025,RMVar_hsa_circ_135098,RMVar_hsa_circ_291833,RMVar_hsa_circ_61756,RMVar_hsa_circ_135099,RMVar_hsa_circ_363486 15729 RMVar_ID_15729 Human_SNP_ID_27177564 A-to-I Human chr1 - 108944918 108944918 108944918 TTATAGAAGATAACTACTGTGAGGCCGGGTGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGG TTATAGAAGATAACTACTGTGAGGCCGGGTGCCGTGGCTCACGCCTGTAATCCCAGCACTTTGGG T G CLCC1,AKNAD1 Ensembl:ENSG00000121940,Ensembl:ENSG00000162641 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs538936792 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28139,RMVar_hsa_circ_53675,RMVar_hsa_circ_305025,RMVar_hsa_circ_135098,RMVar_hsa_circ_291833,RMVar_hsa_circ_61756,RMVar_hsa_circ_135099,RMVar_hsa_circ_363486 15730 RMVar_ID_15730 Human_SNP_ID_27179138 A-to-I Human chr1 - 108951894 108951894 108951894 GGTGTGGTGTAAGCTTGTAGTCCCAGCTACTCAGGAGGCTGAGGTGGGCCGATCACTTGAGTCTG GGTGTGGTGTAAGCTTGTAGTCCCAGCTACTCGGGAGGCTGAGGTGGGCCGATCACTTGAGTCTG T C CLCC1,AKNAD1 Ensembl:ENSG00000121940,Ensembl:ENSG00000162641 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1414333690 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24569072 RMVar_hsa_circ_135099 15731 RMVar_ID_15731 Human_SNP_ID_27179814 A-to-I Human chr1 - 108954414 108954414 108954414 CTCACTGCAGCCTCCGTCCCCCACCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGC CTCACTGCAGCCTCCGTCCCCCACCCAGGTTCCAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGC T G CLCC1,AKNAD1 Ensembl:ENSG00000121940,Ensembl:ENSG00000162641 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs535044248 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_135099 15732 RMVar_ID_15732 Human_SNP_ID_27179984 A-to-I Human chr1 - 108954960 108954960 108954960 GGGTATGGTGGCACATGCCTATAATCCCAGCTACTTGGGAGGGTGAGGCAGGAGAATTTTTGAAC GGGTATGGTGGCACATGCCTATAATCCCAGCTGCTTGGGAGGGTGAGGCAGGAGAATTTTTGAAC T C CLCC1,AKNAD1 Ensembl:ENSG00000121940,Ensembl:ENSG00000162641 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1437176624 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_135099 15733 RMVar_ID_15733 Human_SNP_ID_27179988 A-to-I Human chr1 - 108954972 108954972 108954972 AAAAAATTAGCTGGGTATGGTGGCACATGCCTATAATCCCAGCTACTTGGGAGGGTGAGGCAGGA AAAAAATTAGCTGGGTATGGTGGCACATGCCTGTAATCCCAGCTACTTGGGAGGGTGAGGCAGGA T C CLCC1,AKNAD1 Ensembl:ENSG00000121940,Ensembl:ENSG00000162641 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs28491009 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24569108 RMVar_hsa_circ_135099 15734 RMVar_ID_15734 Human_SNP_ID_27181414 A-to-I Human chr1 - 108960974 108960974 108960974 AAAACTCAACTGCCTGGCTGGCACAGTGGCTCACCTGTAATCCCAGCACTTTGGGAAGACAAGGC AAAACTCAACTGCCTGGCTGGCACAGTGGCTCGCCTGTAATCCCAGCACTTTGGGAAGACAAGGC T C CLCC1,AKNAD1 Ensembl:ENSG00000121940,Ensembl:ENSG00000162641 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1312208141 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22124063 RMVar_hsa_circ_135099 15735 RMVar_ID_15735 Human_SNP_ID_27207590 A-to-I Human chr1 - 109063514 109063514 109063514 TTGCTTGAACCCAGGAGGCAGAGATTGCAGTGAGCCGAGATGGCGCCACTGCACTCCAGCCTGGG TTGCTTGAACCCAGGAGGCAGAGATTGCAGTGGGCCGAGATGGCGCCACTGCACTCCAGCCTGGG T C TAF13 Ensembl:ENSG00000197780 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs923091654 Functional Loss SNV dbSNP153 33..33 33 - - - 15736 RMVar_ID_15736 Human_SNP_ID_27207595 A-to-I Human chr1 - 109063527 109063527 109063527 TGAGGCAGAAGAATTGCTTGAACCCAGGAGGCAGAGATTGCAGTGAGCCGAGATGGCGCCACTGC TGAGGCAGAAGAATTGCTTGAACCCAGGAGGCGGAGATTGCAGTGAGCCGAGATGGCGCCACTGC T C TAF13 Ensembl:ENSG00000197780 Protein coding intron GSE38233;GSE112787;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;293 Flip-In T-REx cells,empty vector;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29967493,31158229,31158229,31158229 RNA-Seq:(High) rs975619142 Functional Loss SNV dbSNP153 33..33 33 - - - 15737 RMVar_ID_15737 Human_SNP_ID_27207596 A-to-I Human chr1 - 109063534 109063534 109063534 GGGAGGCTGAGGCAGAAGAATTGCTTGAACCCAGGAGGCAGAGATTGCAGTGAGCCGAGATGGCG GGGAGGCTGAGGCAGAAGAATTGCTTGAACCCGGGAGGCAGAGATTGCAGTGAGCCGAGATGGCG T C TAF13 Ensembl:ENSG00000197780 Protein coding intron GSE38233;GSE112787;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;293 Flip-In T-REx cells,empty vector;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29967493,31158229,31158229,31158229 RNA-Seq:(High) rs1382457161 Functional Loss SNV dbSNP153 33..33 33 - - - 15738 RMVar_ID_15738 Human_SNP_ID_27207611 A-to-I Human chr1 - 109063609 109063608 109063609 GGCAAAACCTCACCTCTACTAAAAATTAAAAAATTAGCCAGGCATGGAGGCATGTGCCTGTAATC GGCAAAACCTCACCTCTACTAAAAATTAAAAA_TTAGCCAGGCATGGAGGCATGTGCCTGTAATC AT A TAF13 Ensembl:ENSG00000197780 Protein coding intron GSE100210;GSE112787 HepG2 cell line;293 Flip-In T-REx cells,empty vector - 29129909,29967493 RNA-Seq:(High) rs1352636790 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_17720227 15739 RMVar_ID_15739 Human_SNP_ID_27207612 A-to-I Human chr1 - 109063614 109063614 109063614 AACATGGCAAAACCTCACCTCTACTAAAAATTAAAAAATTAGCCAGGCATGGAGGCATGTGCCTG AACATGGCAAAACCTCACCTCTACTAAAAATTTAAAAATTAGCCAGGCATGGAGGCATGTGCCTG T A TAF13 Ensembl:ENSG00000197780 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1308852551 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17720227 15740 RMVar_ID_15740 Human_SNP_ID_27207616 A-to-I Human chr1 - 109063618 109063618 109063618 GGCCAACATGGCAAAACCTCACCTCTACTAAAAATTAAAAAATTAGCCAGGCATGGAGGCATGTG GGCCAACATGGCAAAACCTCACCTCTACTAAATATTAAAAAATTAGCCAGGCATGGAGGCATGTG T A TAF13 Ensembl:ENSG00000197780 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1405918363 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17720227 15741 RMVar_ID_15741 Human_SNP_ID_27207618 A-to-I Human chr1 - 109063638 109063638 109063638 CAGGAGTTCCAGACCAGCCTGGCCAACATGGCAAAACCTCACCTCTACTAAAAATTAAAAAATTA CAGGAGTTCCAGACCAGCCTGGCCAACATGGCGAAACCTCACCTCTACTAAAAATTAAAAAATTA T C TAF13 Ensembl:ENSG00000197780 Protein coding intron GSE38233;GSE112787 cultured B-cells;293 Flip-In T-REx cells,empty vector - 24183664,29967493 RNA-Seq:(High) rs953106443 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17720227 15742 RMVar_ID_15742 Human_SNP_ID_27207626 A-to-I Human chr1 - 109063684 109063684 109063684 TAATCCCAGCACTTTGGGAGGCTGAGGCGGGCAGATCACTTGAGGCCAGGAGTTCCAGACCAGCC TAATCCCAGCACTTTGGGAGGCTGAGGCGGGCGGATCACTTGAGGCCAGGAGTTCCAGACCAGCC T C TAF13 Ensembl:ENSG00000197780 Protein coding intron GSE112787;GSE107867;GSE107867 293 Flip-In T-REx cells,empty vector;ASD brains,Fragile X samples from NIH NeuroBioBank;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 29967493,30559470,30559470 RNA-Seq:(High) rs940365932 Functional Loss SNV dbSNP153 33..33 33 - - - 15743 RMVar_ID_15743 Human_SNP_ID_27207632 A-to-I Human chr1 - 109063715 109063715 109063715 GAACTAGGCCGGGCGTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGCAG GAACTAGGCCGGGCGTGGTGGCTCACACCTGTGATCCCAGCACTTTGGGAGGCTGAGGCGGGCAG T C TAF13 Ensembl:ENSG00000197780 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1056057519 Functional Loss SNV dbSNP153 33..33 33 - - - 15744 RMVar_ID_15744 Human_SNP_ID_27207635 A-to-I Human chr1 - 109063721 109063721 109063721 GATAATGAACTAGGCCGGGCGTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGC GATAATGAACTAGGCCGGGCGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGC T C TAF13 Ensembl:ENSG00000197780 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1230492729 Functional Loss SNV dbSNP153 33..33 33 - - - 15745 RMVar_ID_15745 Human_SNP_ID_27207694 A-to-I Human chr1 - 109063973 109063973 109063973 TTTTGTATTTTTAATAGTGACGGGGTTTCACCATGGTAGCCAGGATGGTTTTGATCTCTTGACCT TTTTGTATTTTTAATAGTGACGGGGTTTCACCGTGGTAGCCAGGATGGTTTTGATCTCTTGACCT T C TAF13 Ensembl:ENSG00000197780 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs543264315 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5665846,Human_RBP_ID_10505696 15746 RMVar_ID_15746 Human_SNP_ID_27207696 A-to-I Human chr1 - 109063976 109063976 109063976 ACTTTTTGTATTTTTAATAGTGACGGGGTTTCACCATGGTAGCCAGGATGGTTTTGATCTCTTGA ACTTTTTGTATTTTTAATAGTGACGGGGTTTCGCCATGGTAGCCAGGATGGTTTTGATCTCTTGA T C TAF13 Ensembl:ENSG00000197780 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934632045 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5665846,Human_RBP_ID_10505696 15747 RMVar_ID_15747 Human_SNP_ID_27207704 A-to-I Human chr1 - 109063990 109063990 109063990 ACCACGCCTGGCTAACTTTTTGTATTTTTAATAGTGACGGGGTTTCACCATGGTAGCCAGGATGG ACCACGCCTGGCTAACTTTTTGTATTTTTAATGGTGACGGGGTTTCACCATGGTAGCCAGGATGG T C TAF13 Ensembl:ENSG00000197780 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs888581130 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5665846,Human_RBP_ID_10505696 15748 RMVar_ID_15748 Human_SNP_ID_27207719 A-to-I Human chr1 - 109064035 109064035 109064035 TCCTTCCTCAGCCTCTCGAGTAGCTGGGAAGTACAGGCGCCTGCCACCACGCCTGGCTAACTTTT TCCTTCCTCAGCCTCTCGAGTAGCTGGGAAGTGCAGGCGCCTGCCACCACGCCTGGCTAACTTTT T C TAF13 Ensembl:ENSG00000197780 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1035289010 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26386202 15749 RMVar_ID_15749 Human_SNP_ID_27207721 A-to-I Human chr1 - 109064046 109064046 109064046 TCAAGTGATTCTCCTTCCTCAGCCTCTCGAGTAGCTGGGAAGTACAGGCGCCTGCCACCACGCCT TCAAGTGATTCTCCTTCCTCAGCCTCTCGAGTGGCTGGGAAGTACAGGCGCCTGCCACCACGCCT T C TAF13 Ensembl:ENSG00000197780 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1347613275 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26386202 15750 RMVar_ID_15750 Human_SNP_ID_27207742 A-to-I Human chr1 - 109064140 109064140 109064140 TTTTTTTTTTTTTTTTGAGATGGAGTCTCACTATGTTGGCAGGCTGGAGTGCAGTGGCGTGATCT TTTTTTTTTTTTTTTTGAGATGGAGTCTCACTGTGTTGGCAGGCTGGAGTGCAGTGGCGTGATCT T C TAF13 Ensembl:ENSG00000197780 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350342464 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5665848,Human_RBP_ID_17674396,Human_RBP_ID_22369420,Human_RBP_ID_26386203 15751 RMVar_ID_15751 Human_SNP_ID_27207743 A-to-I Human chr1 - 109064140 109064140 109064140 TTTTTTTTTTTTTTTTGAGATGGAGTCTCACTATGTTGGCAGGCTGGAGTGCAGTGGCGTGATCT TTTTTTTTTTTTTTTTGAGATGGAGTCTCACTCTGTTGGCAGGCTGGAGTGCAGTGGCGTGATCT T G TAF13 Ensembl:ENSG00000197780 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350342464 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5665848,Human_RBP_ID_17674396,Human_RBP_ID_22369420,Human_RBP_ID_26386203 15752 RMVar_ID_15752 Human_SNP_ID_27207747 A-to-I Human chr1 - 109064143 109064143 109064143 TTTTTTTTTTTTTTTTTTTGAGATGGAGTCTCACTATGTTGGCAGGCTGGAGTGCAGTGGCGTGA TTTTTTTTTTTTTTTTTTTGAGATGGAGTCTCGCTATGTTGGCAGGCTGGAGTGCAGTGGCGTGA T C TAF13 Ensembl:ENSG00000197780 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1295880247 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5665848,Human_RBP_ID_17674396,Human_RBP_ID_22369420,Human_RBP_ID_26386203 15753 RMVar_ID_15753 Human_SNP_ID_27208948 A-to-I Human chr1 - 109068341 109068341 109068341 CTTGAGGCCAGGAATTCAAGACTATCTGGGCAACGTGGCAAAACCCTGACTCTACTAAAAAATAC CTTGAGGCCAGGAATTCAAGACTATCTGGGCAGCGTGGCAAAACCCTGACTCTACTAAAAAATAC T C TAF13 Ensembl:ENSG00000197780 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1270793570 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84646,RMVar_hsa_circ_135135 15754 RMVar_ID_15754 Human_SNP_ID_27208960 A-to-I Human chr1 - 109068423 109068423 109068423 TCTAGAAAAAATTTTAAATGGCTGGGTGTGGTAGCTTAGGCCTGTAATCCCAATAATTTGGGAGG TCTAGAAAAAATTTTAAATGGCTGGGTGTGGTGGCTTAGGCCTGTAATCCCAATAATTTGGGAGG T C TAF13 Ensembl:ENSG00000197780 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs937551663 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84646,RMVar_hsa_circ_135135 15755 RMVar_ID_15755 Human_SNP_ID_27209091 A-to-I Human chr1 - 109068880 109068880 109068880 CTCCTGCCTCAGCCTCCCAAATAGCTGGGATTACAGGTGCGTGCCACCACGCCCCCCTAATTTTT CTCCTGCCTCAGCCTCCCAAATAGCTGGGATTCCAGGTGCGTGCCACCACGCCCCCCTAATTTTT T G TAF13 Ensembl:ENSG00000197780 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1021872812 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84646,RMVar_hsa_circ_135135 15756 RMVar_ID_15756 Human_SNP_ID_27209093 A-to-I Human chr1 - 109068902 109068902 109068902 TGCCTCCTGGGTTCAAGCTATTCTCCTGCCTCAGCCTCCCAAATAGCTGGGATTACAGGTGCGTG TGCCTCCTGGGTTCAAGCTATTCTCCTGCCTCGGCCTCCCAAATAGCTGGGATTACAGGTGCGTG T C TAF13 Ensembl:ENSG00000197780 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1195237158 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84646,RMVar_hsa_circ_135135 15757 RMVar_ID_15757 Human_SNP_ID_27209442 A-to-I Human chr1 - 109070184 109070184 109070184 AAAGCGTCAAGGTTTTGAAAGATGAAAAAGTCAAGGAACTATCGGATTCGAGGGAACTAAGGAGG AAAGCGTCAAGGTTTTGAAAGATGAAAAAGTCTAGGAACTATCGGATTCGAGGGAACTAAGGAGG T A TAF13 Ensembl:ENSG00000197780 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2358956 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_1139,GWAS_ID_1140 RMVar_hsa_circ_84646,RMVar_hsa_circ_135135 15758 RMVar_ID_15758 Human_SNP_ID_27209443 A-to-I Human chr1 - 109070184 109070184 109070184 AAAGCGTCAAGGTTTTGAAAGATGAAAAAGTCAAGGAACTATCGGATTCGAGGGAACTAAGGAGG AAAGCGTCAAGGTTTTGAAAGATGAAAAAGTCGAGGAACTATCGGATTCGAGGGAACTAAGGAGG T C TAF13 Ensembl:ENSG00000197780 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2358956 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_1139,GWAS_ID_1140 RMVar_hsa_circ_84646,RMVar_hsa_circ_135135 15759 RMVar_ID_15759 Human_SNP_ID_27209643 A-to-I Human chr1 - 109071046 109071046 109071046 GTGATCCTCCTGCCTCAGCCTCCCAAAGTGCTAGGATTACAGGCATGAGCCGCCAGACACTGTTT GTGATCCTCCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCGCCAGACACTGTTT T C TAF13 Ensembl:ENSG00000197780 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904299893 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84646,RMVar_hsa_circ_135135 15760 RMVar_ID_15760 Human_SNP_ID_27215188 A-to-I Human chr1 - 109090023 109090023 109090023 CGTCTCTACTACAAATACAAAATTAGCCGGGCATGGTGGCTCATGCCTGTAATGTAATCCCAGCT CGTCTCTACTACAAATACAAAATTAGCCGGGCGTGGTGGCTCATGCCTGTAATGTAATCCCAGCT T C AL356488.3 Ensembl:ENSG00000273382 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs895272546 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5092141 15761 RMVar_ID_15761 Human_SNP_ID_27238074 A-to-I Human chr1 + 109179863 109179863 109179863 AGGAGGCAGAGGTTGCAGTGAGCCGAGATCACACCATTGCACTCTAGCCTGGGTGACAAGAGGGA AGGAGGCAGAGGTTGCAGTGAGCCGAGATCACGCCATTGCACTCTAGCCTGGGTGACAAGAGGGA A G KIAA1324 Ensembl:ENSG00000116299 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1375313404 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18227 15762 RMVar_ID_15762 Human_SNP_ID_27244831 A-to-I Human chr1 + 109206114 109206114 109206114 TTGGCTCACTGCAGCCTCCCCATCCTGGGTTCAAGTGATCCTTCTGCTTCAGCCTCCCCAGTAGC TTGGCTCACTGCAGCCTCCCCATCCTGGGTTCGAGTGATCCTTCTGCTTCAGCCTCCCCAGTAGC A G KIAA1324 Ensembl:ENSG00000116299 Protein coding 3'UTR GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1381458273 Functional Loss SNV dbSNP153 33..33 33 - - - 15763 RMVar_ID_15763 Human_SNP_ID_27244870 A-to-I Human chr1 + 109206258 109206258 109206258 GCTGGTCTCAAACTCCTGGACTCAAGTGATCCACCCACCTCGGCCTCCCAAAGTGCTGGGATTAC GCTGGTCTCAAACTCCTGGACTCAAGTGATCCGCCCACCTCGGCCTCCCAAAGTGCTGGGATTAC A G KIAA1324 Ensembl:ENSG00000116299 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1295158118 Functional Loss SNV dbSNP153 33..33 33 - - - 15764 RMVar_ID_15764 Human_SNP_ID_27247413 A-to-I Human chr1 + 109217640 109217640 109217640 TGGAATGCAGTGGCATGATCACAGCTCACTGCAGCCTGGACCTCCTGGGCTCAACTGGTCCTCCC TGGAATGCAGTGGCATGATCACAGCTCACTGCGGCCTGGACCTCCTGGGCTCAACTGGTCCTCCC A G SARS1 Ensembl:ENSG00000031698 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1465435524 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_320124 15765 RMVar_ID_15765 Human_SNP_ID_27247419 A-to-I Human chr1 + 109217673 109217673 109217673 GCCTGGACCTCCTGGGCTCAACTGGTCCTCCCACCTCAACCTTCTAAGTAGCTGGGACCACAGGT GCCTGGACCTCCTGGGCTCAACTGGTCCTCCCCCCTCAACCTTCTAAGTAGCTGGGACCACAGGT A C SARS1 Ensembl:ENSG00000031698 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1290776600 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5666132 15766 RMVar_ID_15766 Human_SNP_ID_27247425 A-to-I Human chr1 + 109217702 109217702 109217702 CCCACCTCAACCTTCTAAGTAGCTGGGACCACAGGTGTGCACCACCATGCCCAGCTAATTTTTAA CCCACCTCAACCTTCTAAGTAGCTGGGACCACCGGTGTGCACCACCATGCCCAGCTAATTTTTAA A C SARS1 Ensembl:ENSG00000031698 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs926977153 Functional Loss SNV dbSNP153 33..33 33 - - - 15767 RMVar_ID_15767 Human_SNP_ID_27247438 A-to-I Human chr1 + 109217749 109217748 109217750 TGCCCAGCTAATTTTTAATTTTTTGTAGAGACAGAGTCTCACTTTGTTGCCCAGGCTGGTCTCGA TGCCCAGCTAATTTTTAATTTTTTGTAGAGAC__AGTCTCACTTTGTTGCCCAGGCTGGTCTCGA CAG C SARS1 Ensembl:ENSG00000031698 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1232365804 Functional Loss DEL dbSNP153 33..34 33 - - - 15768 RMVar_ID_15768 Human_SNP_ID_27247716 A-to-I Human chr1 + 109218633 109218633 109218633 TGCCTTCCTGGCCTCGCTGTCTACCACTTCCCACATAGGGCCTCCCGCTCTTTGCTCTAGCTTAT TGCCTTCCTGGCCTCGCTGTCTACCACTTCCCGCATAGGGCCTCCCGCTCTTTGCTCTAGCTTAT A G SARS1 Ensembl:ENSG00000031698 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1556769 Functional Loss SNV dbSNP153 33..33 33 - - - 15769 RMVar_ID_15769 Human_SNP_ID_27247717 A-to-I Human chr1 + 109218633 109218633 109218633 TGCCTTCCTGGCCTCGCTGTCTACCACTTCCCACATAGGGCCTCCCGCTCTTTGCTCTAGCTTAT TGCCTTCCTGGCCTCGCTGTCTACCACTTCCCTCATAGGGCCTCCCGCTCTTTGCTCTAGCTTAT A T SARS1 Ensembl:ENSG00000031698 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1556769 Functional Loss SNV dbSNP153 33..33 33 - - - 15770 RMVar_ID_15770 Human_SNP_ID_27247868 A-to-I Human chr1 + 109219223 109219223 109219223 AGGAGGCGGAGCTTGCAGTGAGCCGAGATCACACCACTGCAGTCCAGCCTGGGCGATAGAGCAAG AGGAGGCGGAGCTTGCAGTGAGCCGAGATCACGCCACTGCAGTCCAGCCTGGGCGATAGAGCAAG A G SARS1 Ensembl:ENSG00000031698 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1452456073 Functional Loss SNV dbSNP153 33..33 33 - - - 15771 RMVar_ID_15771 Human_SNP_ID_27248080 A-to-I Human chr1 + 109219720 109219720 109219720 GTATTTTATTAGAGCTGGGGTTTCACCATGTTAGCCAGGATGGTCTTGATCTCCTGACCTTGTGA GTATTTTATTAGAGCTGGGGTTTCACCATGTTGGCCAGGATGGTCTTGATCTCCTGACCTTGTGA A G SARS1 Ensembl:ENSG00000031698 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982006323 Functional Loss SNV dbSNP153 33..33 33 - - - 15772 RMVar_ID_15772 Human_SNP_ID_27248429 A-to-I Human chr1 + 109221140 109221140 109221140 TGGAATGCAGTGGCGTGACCTCAGCTCACTGCAACCTCCACCTCCCAGGTTCAAGCGATTCTCCT TGGAATGCAGTGGCGTGACCTCAGCTCACTGCGACCTCCACCTCCCAGGTTCAAGCGATTCTCCT A G SARS1 Ensembl:ENSG00000031698 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1188749662 Functional Loss SNV dbSNP153 33..33 33 - - - 15773 RMVar_ID_15773 Human_SNP_ID_27248493 A-to-I Human chr1 + 109221333 109221333 109221333 CGCCCGCCTCGGCCTCCCAAAGTGCTGGTATTACAGGTGTGAGCCACTGCGTCCGGCCACATTTT CGCCCGCCTCGGCCTCCCAAAGTGCTGGTATTGCAGGTGTGAGCCACTGCGTCCGGCCACATTTT A G SARS1 Ensembl:ENSG00000031698 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1035942414 Functional Loss SNV dbSNP153 33..33 33 - - - 15774 RMVar_ID_15774 Human_SNP_ID_27249127 A-to-I Human chr1 + 109223620 109223620 109223620 GAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCCCGTCTCTTCCAAAAACACAAA GAGGTCAGGAGTTCAAGACCAGCCTGGCCAACGTGGTGAAACCCCGTCTCTTCCAAAAACACAAA A G SARS1 Ensembl:ENSG00000031698 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1282063796 Functional Loss SNV dbSNP153 33..33 33 - - - 15775 RMVar_ID_15775 Human_SNP_ID_27249783 A-to-I Human chr1 + 109226485 109226485 109226485 GCAGTCCTCCCACCTCAGCCTCTCAAGTAACTAGGACTATAGACACATGTCACTGTGCCTGGCTA GCAGTCCTCCCACCTCAGCCTCTCAAGTAACTGGGACTATAGACACATGTCACTGTGCCTGGCTA A G SARS1 Ensembl:ENSG00000031698 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1443888620 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10506503 RMVar_hsa_circ_33424,RMVar_hsa_circ_325401,RMVar_hsa_circ_336579,RMVar_hsa_circ_293610,RMVar_hsa_circ_135147,RMVar_hsa_circ_135148 15776 RMVar_ID_15776 Human_SNP_ID_27254361 A-to-I Human chr1 + 109243791 109243790 109243791 TCAGGGCTGCCCTTAAAACAGCCTAGAGACCCAACTGGCCTACCAGATGGTGGCTCCAGGCATAA TCAGGGCTGCCCTTAAAACAGCCTAGAGACCC_ACTGGCCTACCAGATGGTGGCTCCAGGCATAA CA C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355219158 Functional Loss DEL dbSNP153 33..33 33 - - - 15777 RMVar_ID_15777 Human_SNP_ID_27254739 A-to-I Human chr1 + 109245084 109245084 109245084 CTGGTAGCCCAGCTGGGTCTCTAGGCTACTCTAAGGGCAGCTCTAAACTCATTCACTTTACCCAC CTGGTAGCCCAGCTGGGTCTCTAGGCTACTCTGAGGGCAGCTCTAAACTCATTCACTTTACCCAC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs977731941 Functional Loss SNV dbSNP153 33..33 33 - - - 15778 RMVar_ID_15778 Human_SNP_ID_27274172 A-to-I Human chr1 - 109311545 109311545 109311545 CTCCCCATCCTGGTTTCCACCCCGGGCTGGCTAGCTCTGTTGGTTTGAAGACTGACAGCCAGCCT CTCCCCATCCTGGTTTCCACCCCGGGCTGGCTGGCTCTGTTGGTTTGAAGACTGACAGCCAGCCT T C SORT1 Ensembl:ENSG00000134243 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs982400081 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5666365,Human_RBP_ID_8169520,Human_RBP_ID_17222666,Human_RBP_ID_17456273,Human_RBP_ID_17720400 15779 RMVar_ID_15779 Human_SNP_ID_27283764 A-to-I Human chr1 - 109349650 109349650 109349650 CTTCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCATGTGCCACCATGCCTAGCTAATTTTT CTTCTGCCTCAGCCTCCCAAGTAGCTGGGACTGCAGGCATGTGCCACCATGCCTAGCTAATTTTT T C SORT1 Ensembl:ENSG00000134243 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1426717499 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7929,RMVar_hsa_circ_84435,RMVar_hsa_circ_135182,RMVar_hsa_circ_39956,RMVar_hsa_circ_291107,RMVar_hsa_circ_322932,RMVar_hsa_circ_135193,RMVar_hsa_circ_370513,RMVar_hsa_circ_127989,RMVar_hsa_circ_135195,RMVar_hsa_circ_90510,RMVar_hsa_circ_135196,RMVar_hsa_circ_341410,RMVar_hsa_circ_135194,RMVar_hsa_circ_265249,RMVar_hsa_circ_43073,RMVar_hsa_circ_298944,RMVar_hsa_circ_350268,RMVar_hsa_circ_53535,RMVar_hsa_circ_135204,RMVar_hsa_circ_135205,RMVar_hsa_circ_68653,RMVar_hsa_circ_336000 15780 RMVar_ID_15780 Human_SNP_ID_27296507 A-to-I Human chr1 - 109403543 109403543 109403543 TCACTGCAGCCACAACCTCCCAGGGTTAAGCAATTCTCCCACCTCAGCCTCCTGAGTACGTGGGA TCACTGCAGCCACAACCTCCCAGGGTTAAGCAGTTCTCCCACCTCAGCCTCCTGAGTACGTGGGA T C PSMA5 Ensembl:ENSG00000143106 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs923716847 Functional Loss SNV dbSNP153 33..33 33 - - - 15781 RMVar_ID_15781 Human_SNP_ID_27296524 A-to-I Human chr1 - 109403624 109403621 109403625 AAATTATTATTAATTAATTTATTGTTTTAGACAGAGCCTCTTTCTGTCACCCAGGCTGGAGTGCA AAATTATTATTAATTAATTTATTGTTTTAGA____GCCTCTTTCTGTCACCCAGGCTGGAGTGCA CTCTG C PSMA5 Ensembl:ENSG00000143106 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs541027294 Functional Loss DEL dbSNP153 32..35 33 - - - 15782 RMVar_ID_15782 Human_SNP_ID_27296526 A-to-I Human chr1 - 109403624 109403624 109403624 AAATTATTATTAATTAATTTATTGTTTTAGACAGAGCCTCTTTCTGTCACCCAGGCTGGAGTGCA AAATTATTATTAATTAATTTATTGTTTTAGACGGAGCCTCTTTCTGTCACCCAGGCTGGAGTGCA T C PSMA5 Ensembl:ENSG00000143106 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1464026683 Functional Loss SNV dbSNP153 33..33 33 - - - 15783 RMVar_ID_15783 Human_SNP_ID_27296644 A-to-I Human chr1 - 109404172 109404172 109404172 CTACAGGCGTGTGCCACCATGCCCGACTAATTATTGTATTTTTAGTAGAGACAGGGTTTTGCCAT CTACAGGCGTGTGCCACCATGCCCGACTAATTGTTGTATTTTTAGTAGAGACAGGGTTTTGCCAT T C PSMA5 Ensembl:ENSG00000143106 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1231376964 Functional Loss SNV dbSNP153 33..33 33 - - - 15784 RMVar_ID_15784 Human_SNP_ID_27296667 A-to-I Human chr1 - 109404260 109404260 109404260 GTTGCCTGGGCTAAGTGCAGTGGTGCGATCTCAGCTCACTGCAACCTCCACATCCCATGTTCGAG GTTGCCTGGGCTAAGTGCAGTGGTGCGATCTCTGCTCACTGCAACCTCCACATCCCATGTTCGAG T A PSMA5 Ensembl:ENSG00000143106 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2152925 Functional Loss SNV dbSNP153 33..33 33 - - - 15785 RMVar_ID_15785 Human_SNP_ID_27296668 A-to-I Human chr1 - 109404260 109404260 109404260 GTTGCCTGGGCTAAGTGCAGTGGTGCGATCTCAGCTCACTGCAACCTCCACATCCCATGTTCGAG GTTGCCTGGGCTAAGTGCAGTGGTGCGATCTCGGCTCACTGCAACCTCCACATCCCATGTTCGAG T C PSMA5 Ensembl:ENSG00000143106 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2152925 Functional Loss SNV dbSNP153 33..33 33 - - - 15786 RMVar_ID_15786 Human_SNP_ID_27297467 A-to-I Human chr1 - 109407779 109407779 109407779 AAATTAGCTGGGTGTGGTGGTGCGTGCCTGTAATCTCAGCTATTCGGGAGGCTGAGGCATGAGAA AAATTAGCTGGGTGTGGTGGTGCGTGCCTGTATTCTCAGCTATTCGGGAGGCTGAGGCATGAGAA T A PSMA5 Ensembl:ENSG00000143106 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs574638492 Functional Loss SNV dbSNP153 33..33 33 - - - 15787 RMVar_ID_15787 Human_SNP_ID_27299947 A-to-I Human chr1 - 109418423 109418423 109418423 TAGTCTTAGCTATTTTGCAGGCTTAGGTGGGAAGATCTCGTGAGCCTGGGAGGTTGGGGCTCCAT TAGTCTTAGCTATTTTGCAGGCTTAGGTGGGACGATCTCGTGAGCCTGGGAGGTTGGGGCTCCAT T G PSMA5 Ensembl:ENSG00000143106 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1039778391 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22563844 RMVar_hsa_circ_135214,RMVar_hsa_circ_348759,RMVar_hsa_circ_121549,RMVar_hsa_circ_299088 15788 RMVar_ID_15788 Human_SNP_ID_27300008 A-to-I Human chr1 - 109418720 109418720 109418720 TTTTTTCCTTGTGGACATTGTTGCTCATCCCTATAATCTCAGTACTTTGGGAGGCTGAGGGAGGA TTTTTTCCTTGTGGACATTGTTGCTCATCCCTGTAATCTCAGTACTTTGGGAGGCTGAGGGAGGA T C PSMA5 Ensembl:ENSG00000143106 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs995592203 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10508078 RMVar_hsa_circ_135214,RMVar_hsa_circ_348759,RMVar_hsa_circ_121549,RMVar_hsa_circ_299088 15789 RMVar_ID_15789 Human_SNP_ID_27301481 A-to-I Human chr1 - 109424378 109424378 109424378 GCTCAGGAGTTGGAGACCAGCCTGGGCAACATAGTGAGACCTCATCTCTACTAAACATTAAAAAA GCTCAGGAGTTGGAGACCAGCCTGGGCAACATGGTGAGACCTCATCTCTACTAAACATTAAAAAA T C PSMA5 Ensembl:ENSG00000143106 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1322269872 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_135214,RMVar_hsa_circ_121549 15790 RMVar_ID_15790 Human_SNP_ID_27312637 A-to-I Human chr1 + 109472148 109472148 109472148 AGATTTTGTTATTCTTTTTCTTTTTTTGAGATAGGGTCTCGCTCTGTCACCCAGGCTGGTGTCCA AGATTTTGTTATTCTTTTTCTTTTTTTGAGATGGGGTCTCGCTCTGTCACCCAGGCTGGTGTCCA A G SYPL2 Ensembl:ENSG00000143028 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs780395310 Functional Loss SNV dbSNP153 33..33 33 - - - 15791 RMVar_ID_15791 Human_SNP_ID_27341054 A-to-I Human chr1 + 109590771 109590771 109590771 GATTTTTAGTAGAGATGTGGTTTCACTAAGTTAGCCAGGCTGGTGTTGAACTCCTGACCTCAAGC GATTTTTAGTAGAGATGTGGTTTCACTAAGTTGGCCAGGCTGGTGTTGAACTCCTGACCTCAAGC A G GNAI3 Ensembl:ENSG00000065135 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1417774431 Functional Loss SNV dbSNP153 33..33 33 - - - 15792 RMVar_ID_15792 Human_SNP_ID_27341068 A-to-I Human chr1 + 109590839 109590839 109590839 CCACCTGCTGCGGCCCCCAAAGTGCAGGGATTACAGATGTGAGCCACCGCACCCAGCTCCTTTTT CCACCTGCTGCGGCCCCCAAAGTGCAGGGATTGCAGATGTGAGCCACCGCACCCAGCTCCTTTTT A G GNAI3 Ensembl:ENSG00000065135 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs551524811 Functional Loss SNV dbSNP153 33..33 33 - - - 15793 RMVar_ID_15793 Human_SNP_ID_27364495 A-to-I Human chr1 + 109688168 109688168 109688168 ATCTCTGACGCGACCTGCGGGCCATCTCTCCCAGCTGGCCCACGCCATCCGCCTGCTCCTGGAAT ATCTCTGACGCGACCTGCGGGCCATCTCTCCCTGCTGGCCCACGCCATCCGCCTGCTCCTGGAAT A T GSTM2,GSTM1 Ensembl:ENSG00000213366,Ensembl:ENSG00000134184 Protein coding,Protein coding intron,intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1275655935 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_107027,Human_Splice_Rec_107041,Human_Splice_Rec_107055,Human_Splice_Rec_107066,Human_Splice_Rec_107067,Human_Splice_Rec_107077,Human_Splice_Rec_107087 RMVar_hsa_circ_135230,RMVar_hsa_circ_106247,RMVar_hsa_circ_79429,RMVar_hsa_circ_135232 15794 RMVar_ID_15794 Human_SNP_ID_27369921 A-to-I Human chr1 + 109713681 109713681 109713681 TGTGGGTGGCAGGTGGGGAGACAGAAGAGGAGAAGATTCGTGTGGACATTTTGGAGAACCAGGTT TGTGGGTGGCAGGTGGGGAGACAGAAGAGGAGGAGATTCGTGTGGACATTTTGGAGAACCAGGTT A G GSTM5 Ensembl:ENSG00000134201 Protein coding CDS GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1202830612 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_107104,Human_Splice_Rec_107105,Human_Splice_Rec_107116,Human_Splice_Rec_107117,Human_Splice_Rec_107126,Human_Splice_Rec_107127,Human_Splice_Rec_107140,Human_Splice_Rec_107141,Human_Splice_Rec_107151 15795 RMVar_ID_15795 Human_SNP_ID_27372285 A-to-I Human chr1 - 109723594 109723594 109723594 GCACTACTGCACTCCAGCTTGGGCGACAGAGCAAGACCTTGTCTAAAAAAAAAAAAAAAAATTAT GCACTACTGCACTCCAGCTTGGGCGACAGAGCGAGACCTTGTCTAAAAAAAAAAAAAAAAATTAT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1464461129 Functional Loss SNV dbSNP153 33..33 33 - - - 15796 RMVar_ID_15796 Human_SNP_ID_27440638 A-to-I Human chr1 + 110004702 110004702 110004702 CTACTCAGGAGGTGGGAAGATTGTTTGAGCCCAGCAGTTTGCAGCCAGCCTGGCAAACATAGTGA CTACTCAGGAGGTGGGAAGATTGTTTGAGCCCCGCAGTTTGCAGCCAGCCTGGCAAACATAGTGA A C AHCYL1 Ensembl:ENSG00000168710 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1387288637 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38762,RMVar_hsa_circ_135235,RMVar_hsa_circ_86921,RMVar_hsa_circ_73907,RMVar_hsa_circ_30452 15797 RMVar_ID_15797 Human_SNP_ID_27526027 A-to-I Human chr1 + 110357662 110357662 110357662 TTTAGTAGAGACGGGGTTTCACCATGATGGCCAGGCTGGTTTCGAACTCCTGAGCTCAAGTGATC TTTAGTAGAGACGGGGTTTCACCATGATGGCCCGGCTGGTTTCGAACTCCTGAGCTCAAGTGATC A C LAMTOR5-AS1 Ensembl:ENSG00000224699 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1461846988 Functional Loss SNV dbSNP153 33..33 33 - - - 15798 RMVar_ID_15798 Human_SNP_ID_27526448 A-to-I Human chr1 + 110359477 110359477 110359477 CCCTGTCCAGCTAATTTTAAACAATTTTTTGTAGAGATGGGGCTCACTGTGTTGCCCAGGCTGGT CCCTGTCCAGCTAATTTTAAACAATTTTTTGTGGAGATGGGGCTCACTGTGTTGCCCAGGCTGGT A G LAMTOR5-AS1 Ensembl:ENSG00000224699 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1316318515 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5668268,Human_RBP_ID_10514183 15799 RMVar_ID_15799 Human_SNP_ID_27526546 A-to-I Human chr1 + 110359967 110359967 110359967 ACAATTAGCTGGGCCTGGTGGCGGGCGTCTGTAATCCCAGCTACTTGGGAGGCTGAGGCATGAAA ACAATTAGCTGGGCCTGGTGGCGGGCGTCTGTGATCCCAGCTACTTGGGAGGCTGAGGCATGAAA A G LAMTOR5-AS1 Ensembl:ENSG00000224699 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355201782 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5668277,Human_RBP_ID_24570785 15800 RMVar_ID_15800 Human_SNP_ID_27527145 A-to-I Human chr1 + 110362450 110362450 110362450 CAGTCTGGCCAAGATGGTAAAACCCTGTCTCTATTAAAAATAACAAAAATTGGCTGGGCATGGTG CAGTCTGGCCAAGATGGTAAAACCCTGTCTCTCTTAAAAATAACAAAAATTGGCTGGGCATGGTG A C LAMTOR5-AS1 Ensembl:ENSG00000224699 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs936434104 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5245155,Human_RBP_ID_8242176,Human_RBP_ID_17720802 15801 RMVar_ID_15801 Human_SNP_ID_27527158 A-to-I Human chr1 + 110362522 110362522 110362522 CCGGTGATCCCAGCTGCTTGGGAGGCTGAGGCAGGAGAATAGCTTGAACTCTGGAGGCGGAGTTT CCGGTGATCCCAGCTGCTTGGGAGGCTGAGGCGGGAGAATAGCTTGAACTCTGGAGGCGGAGTTT A G LAMTOR5-AS1 Ensembl:ENSG00000224699 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1226825669 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5245155 15802 RMVar_ID_15802 Human_SNP_ID_27527390 A-to-I Human chr1 - 110363437 110363437 110363437 TATTTTTAGTAGAGGCGGGGTTTCACCATGTTAGCCAGGATGGTCTCCATCTCCTGACCTCGTGA TATTTTTAGTAGAGGCGGGGTTTCACCATGTTGGCCAGGATGGTCTCCATCTCCTGACCTCGTGA T C SLC16A4 Ensembl:ENSG00000168679 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1326340701 Functional Loss SNV dbSNP153 33..33 33 - - - 15803 RMVar_ID_15803 Human_SNP_ID_27527392 A-to-I Human chr1 - 110363445 110363444 110363445 ATTTTTTGTATTTTTAGTAGAGGCGGGGTTTCACCATGTTAGCCAGGATGGTCTCCATCTCCTGA ATTTTTTGTATTTTTAGTAGAGGCGGGGTTTC_CCATGTTAGCCAGGATGGTCTCCATCTCCTGA GT G SLC16A4 Ensembl:ENSG00000168679 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1277138158 Functional Loss DEL dbSNP153 33..33 33 - - - 15804 RMVar_ID_15804 Human_SNP_ID_27528177 A-to-I Human chr1 + 110366182 110366181 110366183 ACTCACTCACTTTTTTTTTTGTTTTTTGAGACAGAGCCTCGCTCTGTTGCCCAGGCTGGAGTGAG ACTCACTCACTTTTTTTTTTGTTTTTTGAGAC__AGCCTCGCTCTGTTGCCCAGGCTGGAGTGAG CAG C LAMTOR5-AS1 Ensembl:ENSG00000224699 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1252782191 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_2084112,Human_RBP_ID_5245162,Human_RBP_ID_10514603,Human_RBP_ID_23322165 15805 RMVar_ID_15805 Human_SNP_ID_27528254 A-to-I Human chr1 - 110366419 110366419 110366419 CATTCTAAGAGTGAGTGAAATCCAAGCACTTTAGAAGGCTGAGGCAGGCGGATCACCTGAGATCA CATTCTAAGAGTGAGTGAAATCCAAGCACTTTTGAAGGCTGAGGCAGGCGGATCACCTGAGATCA T A SLC16A4 Ensembl:ENSG00000168679 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350891069 Functional Loss SNV dbSNP153 33..33 33 - - - 15806 RMVar_ID_15806 Human_SNP_ID_27528255 A-to-I Human chr1 - 110366419 110366419 110366419 CATTCTAAGAGTGAGTGAAATCCAAGCACTTTAGAAGGCTGAGGCAGGCGGATCACCTGAGATCA CATTCTAAGAGTGAGTGAAATCCAAGCACTTTGGAAGGCTGAGGCAGGCGGATCACCTGAGATCA T C SLC16A4 Ensembl:ENSG00000168679 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350891069 Functional Loss SNV dbSNP153 33..33 33 - - - 15807 RMVar_ID_15807 Human_SNP_ID_27528457 A-to-I Human chr1 + 110367385 110367385 110367385 TGGGTGTTGGCCAGGCGTGACGGCTCATGCCTATAATCTTAGCACTTTGGGAGGCCAAGGTAGAA TGGGTGTTGGCCAGGCGTGACGGCTCATGCCTGTAATCTTAGCACTTTGGGAGGCCAAGGTAGAA A G LAMTOR5-AS1 Ensembl:ENSG00000224699 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1045879177 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10514690 15808 RMVar_ID_15808 Human_SNP_ID_27528458 A-to-I Human chr1 + 110367387 110367387 110367387 GGTGTTGGCCAGGCGTGACGGCTCATGCCTATAATCTTAGCACTTTGGGAGGCCAAGGTAGAAGG GGTGTTGGCCAGGCGTGACGGCTCATGCCTATCATCTTAGCACTTTGGGAGGCCAAGGTAGAAGG A C LAMTOR5-AS1 Ensembl:ENSG00000224699 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs906039031 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10514690 15809 RMVar_ID_15809 Human_SNP_ID_27528462 A-to-I Human chr1 - 110367398 110367397 110367398 GCTCAAGTCATCCTTCTACCTTGGCCTCCCAAAGTGCTAAGATTATAGGCATGAGCCGTCACGCC GCTCAAGTCATCCTTCTACCTTGGCCTCCCAA_GTGCTAAGATTATAGGCATGAGCCGTCACGCC CT C SLC16A4 Ensembl:ENSG00000168679 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1374191765 Functional Loss DEL dbSNP153 33..33 33 - - - 15810 RMVar_ID_15810 Human_SNP_ID_27528898 A-to-I Human chr1 + 110369390 110369390 110369390 GGGAGGCCGATGTGGGCGGATTGCTTGAGCTCAGTAGTTCGAGACCAGCCTGGGCAAAATGGTGA GGGAGGCCGATGTGGGCGGATTGCTTGAGCTCCGTAGTTCGAGACCAGCCTGGGCAAAATGGTGA A C LAMTOR5-AS1 Ensembl:ENSG00000224699 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs777737468 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10514785,Human_RBP_ID_17557275,Human_RBP_ID_24750108 15811 RMVar_ID_15811 Human_SNP_ID_27539937 A-to-I Human chr1 + 110411941 110411941 110411941 CAGGCTGGAGTGCAGTGGCACAATCTTGGCTCACTGCAACCTCTGCCTCCTGAGCTCGTGATTCA CAGGCTGGAGTGCAGTGGCACAATCTTGGCTCGCTGCAACCTCTGCCTCCTGAGCTCGTGATTCA A G LAMTOR5-AS1 Ensembl:ENSG00000224699 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs964274094 Functional Loss SNV dbSNP153 33..33 33 - - - 15812 RMVar_ID_15812 Human_SNP_ID_27539964 A-to-I Human chr1 + 110412066 110412066 110412066 TTTTTGTAGAGATGGGGTTTTGCCATGTTGCCAGGCTGGTCTCGAACTCCTGCAATTTGCTCTCC TTTTTGTAGAGATGGGGTTTTGCCATGTTGCCTGGCTGGTCTCGAACTCCTGCAATTTGCTCTCC A T LAMTOR5-AS1 Ensembl:ENSG00000224699 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1296076720 Functional Loss SNV dbSNP153 33..33 33 - - - 15813 RMVar_ID_15813 Human_SNP_ID_27585221 A-to-I Human chr1 - 110597726 110597722 110597726 AAAATCTTGCTCTCAGGACTGAAAAGTGATAGATAGTACCTGGATTATCAGATAATGCCCTTGAC AAAATCTTGCTCTCAGGACTGAAAAGTGATAG____TACCTGGATTATCAGATAATGCCCTTGAC ACTAT A KCNA2 Ensembl:ENSG00000177301 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1189201499 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_18174343 15814 RMVar_ID_15814 Human_SNP_ID_27708651 A-to-I Human chr1 + 111121225 111121225 111121225 TTTCCATTTAAATTCAATTTAACTGTAAATAAAATTTAAAGACTCAAGAAATTAAAATATTCTCC TTTCCATTTAAATTCAATTTAACTGTAAATAACATTTAAAGACTCAAGAAATTAAAATATTCTCC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1333926837 Functional Loss SNV dbSNP153 33..33 33 - - - 15815 RMVar_ID_15815 Human_SNP_ID_27711481 A-to-I Human chr1 - 111133310 111133310 111133310 AGCCGGACGTGGTGGCAGATGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCTCT AGCCGGACGTGGTGGCAGATGCCTGTAATCCCCGCTACTCAGGAGGCTGAGGCAGGAGAATCTCT T G DRAM2 Ensembl:ENSG00000156171 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1444351770 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_303665,RMVar_hsa_circ_307841,RMVar_hsa_circ_326947,RMVar_hsa_circ_120464,RMVar_hsa_circ_288603,RMVar_hsa_circ_135269,RMVar_hsa_circ_50523,RMVar_hsa_circ_135268,RMVar_hsa_circ_364938 15816 RMVar_ID_15816 Human_SNP_ID_27711483 A-to-I Human chr1 - 111133316 111133316 111133316 AAGATTAGCCGGACGTGGTGGCAGATGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA AAGATTAGCCGGACGTGGTGGCAGATGCCTGTGATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA T C DRAM2 Ensembl:ENSG00000156171 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285461297 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24571623 RMVar_hsa_circ_303665,RMVar_hsa_circ_307841,RMVar_hsa_circ_326947,RMVar_hsa_circ_120464,RMVar_hsa_circ_288603,RMVar_hsa_circ_135269,RMVar_hsa_circ_50523,RMVar_hsa_circ_135268,RMVar_hsa_circ_364938 15817 RMVar_ID_15817 Human_SNP_ID_27786486 A-to-I Human chr1 - 111436590 111436590 111436590 CCAGCACTTTTGGAGGCTGAGGTGGACAGATCACTTGAGCTCAGGAATTCGAGACCAGCCTGGGC CCAGCACTTTTGGAGGCTGAGGTGGACAGATCTCTTGAGCTCAGGAATTCGAGACCAGCCTGGGC T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1253621595 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24572033 15818 RMVar_ID_15818 Human_SNP_ID_28031073 A-to-I Human chr1 + 112425063 112425063 112425063 CCAGGTTGGTCTCGAACTCCTGGCCTGGACCCAAGTGATCCTCCCACCTCACCCTCCCAAAGTGC CCAGGTTGGTCTCGAACTCCTGGCCTGGACCCCAGTGATCCTCCCACCTCACCCTCCCAAAGTGC A C CTTNBP2NL Ensembl:ENSG00000143079 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs183458374 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_30696,RMVar_hsa_circ_30643,RMVar_hsa_circ_346229,RMVar_hsa_circ_135314 15819 RMVar_ID_15819 Human_SNP_ID_28031076 A-to-I Human chr1 + 112425076 112425076 112425076 GAACTCCTGGCCTGGACCCAAGTGATCCTCCCACCTCACCCTCCCAAAGTGCTGGGATTACAAGC GAACTCCTGGCCTGGACCCAAGTGATCCTCCCGCCTCACCCTCCCAAAGTGCTGGGATTACAAGC A G CTTNBP2NL Ensembl:ENSG00000143079 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1211617415 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_30696,RMVar_hsa_circ_30643,RMVar_hsa_circ_346229,RMVar_hsa_circ_135314 15820 RMVar_ID_15820 Human_SNP_ID_28033550 A-to-I Human chr1 + 112435087 112435087 112435087 ATCACTTGAACCCAGGAGGCAGAGATTGTAGCAAGCCGAGATCACACCATTGCACTCCAGCCTGG ATCACTTGAACCCAGGAGGCAGAGATTGTAGCGAGCCGAGATCACACCATTGCACTCCAGCCTGG A G CTTNBP2NL Ensembl:ENSG00000143079 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs901108794 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24572738 RMVar_hsa_circ_30696,RMVar_hsa_circ_30643,RMVar_hsa_circ_346229,RMVar_hsa_circ_135314 15821 RMVar_ID_15821 Human_SNP_ID_28047576 A-to-I Human chr1 + 112494405 112494405 112494405 AATATATATATTTTAAGACACGGTCTTGCTCTATCACCCAGGCTAGAGTACAGTGGCACAATCAT AATATATATATTTTAAGACACGGTCTTGCTCTGTCACCCAGGCTAGAGTACAGTGGCACAATCAT A G WNT2B Ensembl:ENSG00000134245 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs759637830 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_135315 15822 RMVar_ID_15822 Human_SNP_ID_28048727 A-to-I Human chr1 + 112499155 112499155 112499155 TTGAACCCAGGAGGTGGAGGTTGCAGTGAGCCAAGATCACGCCACTGCACTCCAGCCTGGGCGAC TTGAACCCAGGAGGTGGAGGTTGCAGTGAGCCGAGATCACGCCACTGCACTCCAGCCTGGGCGAC A G WNT2B Ensembl:ENSG00000134245 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1228229743 Functional Loss SNV dbSNP153 33..33 33 - - - 15823 RMVar_ID_15823 Human_SNP_ID_28057759 A-to-I Human chr1 - 112539426 112539426 112539426 GTCTCGAACTTCTGACCTCAAGTGATCAACCCACCTTGGCCTCCCAAAGTGCTGGGACTACAGGC GTCTCGAACTTCTGACCTCAAGTGATCAACCCGCCTTGGCCTCCCAAAGTGCTGGGACTACAGGC T C ST7L Ensembl:ENSG00000007341 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs528858790 Functional Loss SNV dbSNP153 33..33 33 - - - 15824 RMVar_ID_15824 Human_SNP_ID_28063636 A-to-I Human chr1 - 112565375 112565375 112565375 AAATTCGCTATCTGTAGCATTTAAAAGTTACTATTTTGGCTGGGCGTGGTGGCTCACGCCTGCAA AAATTCGCTATCTGTAGCATTTAAAAGTTACTGTTTTGGCTGGGCGTGGTGGCTCACGCCTGCAA T C ST7L Ensembl:ENSG00000007341 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1186409052 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36720,RMVar_hsa_circ_11183,RMVar_hsa_circ_330132,RMVar_hsa_circ_353572,RMVar_hsa_circ_361342,RMVar_hsa_circ_365817,RMVar_hsa_circ_355908,RMVar_hsa_circ_346109,RMVar_hsa_circ_332808,RMVar_hsa_circ_135316,RMVar_hsa_circ_135317,RMVar_hsa_circ_346343,RMVar_hsa_circ_350204,RMVar_hsa_circ_365708,RMVar_hsa_circ_342692,RMVar_hsa_circ_49278,RMVar_hsa_circ_27626,RMVar_hsa_circ_29477,RMVar_hsa_circ_309974,RMVar_hsa_circ_353145,RMVar_hsa_circ_135319,RMVar_hsa_circ_355430,RMVar_hsa_circ_331514,RMVar_hsa_circ_336116,RMVar_hsa_circ_88968,RMVar_hsa_circ_309124,RMVar_hsa_circ_49290,RMVar_hsa_circ_135323,RMVar_hsa_circ_135325,RMVar_hsa_circ_135326,RMVar_hsa_circ_135324,RMVar_hsa_circ_135322,RMVar_hsa_circ_296508,RMVar_hsa_circ_334942,RMVar_hsa_circ_343283,RMVar_hsa_circ_345948,RMVar_hsa_circ_339188,RMVar_hsa_circ_325474,RMVar_hsa_circ_267326,RMVar_hsa_circ_293455,RMVar_hsa_circ_72659,RMVar_hsa_circ_135327,RMVar_hsa_circ_135329,RMVar_hsa_circ_12995,RMVar_hsa_circ_135330,RMVar_hsa_circ_135328 15825 RMVar_ID_15825 Human_SNP_ID_28063738 A-to-I Human chr1 - 112565868 112565867 112565869 TAGCTGGGACTACAGGTGCATGCCACGGAGCTAATTTTTGTATTTTTTGTAGAGATGGGGTTTTG TAGCTGGGACTACAGGTGCATGCCACGGAGC__ATTTTTGTATTTTTTGTAGAGATGGGGTTTTG TTA T ST7L Ensembl:ENSG00000007341 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1446909599 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_36720,RMVar_hsa_circ_11183,RMVar_hsa_circ_330132,RMVar_hsa_circ_353572,RMVar_hsa_circ_361342,RMVar_hsa_circ_365817,RMVar_hsa_circ_355908,RMVar_hsa_circ_346109,RMVar_hsa_circ_332808,RMVar_hsa_circ_135316,RMVar_hsa_circ_135317,RMVar_hsa_circ_346343,RMVar_hsa_circ_350204,RMVar_hsa_circ_365708,RMVar_hsa_circ_342692,RMVar_hsa_circ_49278,RMVar_hsa_circ_27626,RMVar_hsa_circ_29477,RMVar_hsa_circ_309974,RMVar_hsa_circ_353145,RMVar_hsa_circ_135319,RMVar_hsa_circ_355430,RMVar_hsa_circ_331514,RMVar_hsa_circ_336116,RMVar_hsa_circ_88968,RMVar_hsa_circ_309124,RMVar_hsa_circ_49290,RMVar_hsa_circ_135323,RMVar_hsa_circ_135325,RMVar_hsa_circ_135326,RMVar_hsa_circ_135324,RMVar_hsa_circ_135322,RMVar_hsa_circ_296508,RMVar_hsa_circ_334942,RMVar_hsa_circ_343283,RMVar_hsa_circ_345948,RMVar_hsa_circ_339188,RMVar_hsa_circ_325474,RMVar_hsa_circ_267326,RMVar_hsa_circ_293455,RMVar_hsa_circ_72659,RMVar_hsa_circ_135327,RMVar_hsa_circ_135329,RMVar_hsa_circ_12995,RMVar_hsa_circ_135330,RMVar_hsa_circ_135328 15826 RMVar_ID_15826 Human_SNP_ID_28065934 A-to-I Human chr1 - 112574043 112574043 112574043 GGGTGTGGTGGGGTGCGCCTGTAGTCCCAGCTACTTGGGGGGCTGAGGCAGGAGAATCACTTGAG GGGTGTGGTGGGGTGCGCCTGTAGTCCCAGCTGCTTGGGGGGCTGAGGCAGGAGAATCACTTGAG T C ST7L Ensembl:ENSG00000007341 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs936851582 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36720,RMVar_hsa_circ_11183,RMVar_hsa_circ_330132,RMVar_hsa_circ_353572,RMVar_hsa_circ_361342,RMVar_hsa_circ_365817,RMVar_hsa_circ_355908,RMVar_hsa_circ_346109,RMVar_hsa_circ_332808,RMVar_hsa_circ_135316,RMVar_hsa_circ_135317,RMVar_hsa_circ_346343,RMVar_hsa_circ_350204,RMVar_hsa_circ_365708,RMVar_hsa_circ_342692,RMVar_hsa_circ_49278,RMVar_hsa_circ_27626,RMVar_hsa_circ_29477,RMVar_hsa_circ_309974,RMVar_hsa_circ_353145,RMVar_hsa_circ_135319,RMVar_hsa_circ_355430,RMVar_hsa_circ_331514,RMVar_hsa_circ_336116,RMVar_hsa_circ_88968,RMVar_hsa_circ_309124,RMVar_hsa_circ_49290,RMVar_hsa_circ_135323,RMVar_hsa_circ_135325,RMVar_hsa_circ_135326,RMVar_hsa_circ_135324,RMVar_hsa_circ_135322,RMVar_hsa_circ_296508,RMVar_hsa_circ_334942,RMVar_hsa_circ_343283,RMVar_hsa_circ_345948,RMVar_hsa_circ_339188,RMVar_hsa_circ_325474,RMVar_hsa_circ_267326,RMVar_hsa_circ_293455,RMVar_hsa_circ_72659,RMVar_hsa_circ_135327,RMVar_hsa_circ_135329,RMVar_hsa_circ_135330,RMVar_hsa_circ_135328 15827 RMVar_ID_15827 Human_SNP_ID_28066325 A-to-I Human chr1 - 112575231 112575231 112575231 TGAGTACTGTAAACTTTTATTTTTCTTTAGACAGAGTTTTGCTTTCGCCCAAGCTGGAGTACAGT TGAGTACTGTAAACTTTTATTTTTCTTTAGACTGAGTTTTGCTTTCGCCCAAGCTGGAGTACAGT T A ST7L Ensembl:ENSG00000007341 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs754054302 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2085178 RMVar_hsa_circ_36720,RMVar_hsa_circ_11183,RMVar_hsa_circ_330132,RMVar_hsa_circ_353572,RMVar_hsa_circ_361342,RMVar_hsa_circ_365817,RMVar_hsa_circ_355908,RMVar_hsa_circ_346109,RMVar_hsa_circ_332808,RMVar_hsa_circ_135316,RMVar_hsa_circ_135317,RMVar_hsa_circ_346343,RMVar_hsa_circ_350204,RMVar_hsa_circ_365708,RMVar_hsa_circ_342692,RMVar_hsa_circ_49278,RMVar_hsa_circ_27626,RMVar_hsa_circ_29477,RMVar_hsa_circ_309974,RMVar_hsa_circ_353145,RMVar_hsa_circ_135319,RMVar_hsa_circ_355430,RMVar_hsa_circ_331514,RMVar_hsa_circ_336116,RMVar_hsa_circ_88968,RMVar_hsa_circ_309124,RMVar_hsa_circ_49290,RMVar_hsa_circ_135323,RMVar_hsa_circ_135325,RMVar_hsa_circ_135326,RMVar_hsa_circ_135324,RMVar_hsa_circ_135322,RMVar_hsa_circ_296508,RMVar_hsa_circ_334942,RMVar_hsa_circ_343283,RMVar_hsa_circ_345948,RMVar_hsa_circ_339188,RMVar_hsa_circ_325474,RMVar_hsa_circ_267326,RMVar_hsa_circ_293455,RMVar_hsa_circ_72659,RMVar_hsa_circ_135327,RMVar_hsa_circ_135329,RMVar_hsa_circ_135330,RMVar_hsa_circ_135328 15828 RMVar_ID_15828 Human_SNP_ID_28067762 A-to-I Human chr1 - 112581459 112581452 112581460 GGGAGGTTCAGGCTGTAGTGAGCTGTGACTGCACCACTGTAGTCCAGCCTAGGCGACAGAGGGAG GGGAGGTTCAGGCTGTAGTGAGCTGTGACTG________TAGTCCAGCCTAGGCGACAGAGGGAG ACAGTGGTG A ST7L Ensembl:ENSG00000007341 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404379149 Functional Loss DEL dbSNP153 32..39 33 - - - Human_RBP_ID_1249352 RMVar_hsa_circ_36720,RMVar_hsa_circ_11183,RMVar_hsa_circ_330132,RMVar_hsa_circ_353572,RMVar_hsa_circ_361342,RMVar_hsa_circ_365817,RMVar_hsa_circ_346109,RMVar_hsa_circ_332808,RMVar_hsa_circ_135316,RMVar_hsa_circ_135317,RMVar_hsa_circ_350204,RMVar_hsa_circ_365708,RMVar_hsa_circ_342692,RMVar_hsa_circ_49278,RMVar_hsa_circ_29477,RMVar_hsa_circ_309974,RMVar_hsa_circ_353145,RMVar_hsa_circ_135319,RMVar_hsa_circ_355430,RMVar_hsa_circ_336116,RMVar_hsa_circ_88968,RMVar_hsa_circ_309124,RMVar_hsa_circ_49290,RMVar_hsa_circ_135323,RMVar_hsa_circ_135325,RMVar_hsa_circ_135326,RMVar_hsa_circ_135324,RMVar_hsa_circ_296508,RMVar_hsa_circ_343283,RMVar_hsa_circ_345948,RMVar_hsa_circ_339188,RMVar_hsa_circ_325474,RMVar_hsa_circ_267326,RMVar_hsa_circ_293455,RMVar_hsa_circ_72659,RMVar_hsa_circ_135337,RMVar_hsa_circ_135327,RMVar_hsa_circ_135329,RMVar_hsa_circ_135330,RMVar_hsa_circ_135328,RMVar_hsa_circ_290543,RMVar_hsa_circ_299767,RMVar_hsa_circ_308704,RMVar_hsa_circ_317717,RMVar_hsa_circ_302569,RMVar_hsa_circ_294696,RMVar_hsa_circ_288682,RMVar_hsa_circ_135333,RMVar_hsa_circ_135335,RMVar_hsa_circ_135336,RMVar_hsa_circ_135334,RMVar_hsa_circ_135339,RMVar_hsa_circ_135331,RMVar_hsa_circ_135332,RMVar_hsa_circ_347083,RMVar_hsa_circ_368356,RMVar_hsa_circ_73803 15829 RMVar_ID_15829 Human_SNP_ID_28072408 A-to-I Human chr1 - 112601871 112601871 112601871 TTTTATTATGTTGGCTAGGCTGGTCTTGAACTACTGACCTTAGGTGATCTGCCCACCTTGGCCTC TTTTATTATGTTGGCTAGGCTGGTCTTGAACTCCTGACCTTAGGTGATCTGCCCACCTTGGCCTC T G ST7L Ensembl:ENSG00000007341 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1394071878 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36720,RMVar_hsa_circ_353572,RMVar_hsa_circ_365817,RMVar_hsa_circ_135317,RMVar_hsa_circ_350204,RMVar_hsa_circ_29477,RMVar_hsa_circ_355430,RMVar_hsa_circ_88968,RMVar_hsa_circ_135325,RMVar_hsa_circ_135326,RMVar_hsa_circ_345948,RMVar_hsa_circ_293455,RMVar_hsa_circ_135330,RMVar_hsa_circ_317717,RMVar_hsa_circ_288682,RMVar_hsa_circ_135331,RMVar_hsa_circ_135332,RMVar_hsa_circ_368356,RMVar_hsa_circ_287047,RMVar_hsa_circ_318479,RMVar_hsa_circ_38754,RMVar_hsa_circ_135343,RMVar_hsa_circ_135344,RMVar_hsa_circ_347369,RMVar_hsa_circ_358887,RMVar_hsa_circ_292444,RMVar_hsa_circ_312601,RMVar_hsa_circ_270336,RMVar_hsa_circ_135352,RMVar_hsa_circ_286925,RMVar_hsa_circ_135345,RMVar_hsa_circ_135346,RMVar_hsa_circ_291467,RMVar_hsa_circ_339234,RMVar_hsa_circ_77765,RMVar_hsa_circ_135353,RMVar_hsa_circ_135355,RMVar_hsa_circ_135350,RMVar_hsa_circ_135351,RMVar_hsa_circ_354080,RMVar_hsa_circ_340249,RMVar_hsa_circ_135354 15830 RMVar_ID_15830 Human_SNP_ID_28073817 A-to-I Human chr1 - 112607337 112607337 112607337 CCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCAGGCCTGGCCCATTCTGTCTTCT CCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCAGGCCTGGCCCATTCTGTCTTCT T C ST7L Ensembl:ENSG00000007341 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1174485017 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36720,RMVar_hsa_circ_353572,RMVar_hsa_circ_365817,RMVar_hsa_circ_135317,RMVar_hsa_circ_350204,RMVar_hsa_circ_29477,RMVar_hsa_circ_355430,RMVar_hsa_circ_88968,RMVar_hsa_circ_135325,RMVar_hsa_circ_135326,RMVar_hsa_circ_345948,RMVar_hsa_circ_293455,RMVar_hsa_circ_135330,RMVar_hsa_circ_317717,RMVar_hsa_circ_288682,RMVar_hsa_circ_135331,RMVar_hsa_circ_135332,RMVar_hsa_circ_368356,RMVar_hsa_circ_287047,RMVar_hsa_circ_318479,RMVar_hsa_circ_38754,RMVar_hsa_circ_135343,RMVar_hsa_circ_135344,RMVar_hsa_circ_347369,RMVar_hsa_circ_358887,RMVar_hsa_circ_292444,RMVar_hsa_circ_312601,RMVar_hsa_circ_270336,RMVar_hsa_circ_135352,RMVar_hsa_circ_286925,RMVar_hsa_circ_135345,RMVar_hsa_circ_135346,RMVar_hsa_circ_291467,RMVar_hsa_circ_339234,RMVar_hsa_circ_77765,RMVar_hsa_circ_135353,RMVar_hsa_circ_135355,RMVar_hsa_circ_135350,RMVar_hsa_circ_135351,RMVar_hsa_circ_354080,RMVar_hsa_circ_340249,RMVar_hsa_circ_135354 15831 RMVar_ID_15831 Human_SNP_ID_28073852 A-to-I Human chr1 - 112607488 112607488 112607488 TCAAGCGATTCTCCTGCCCCAGCCTCCCGAGTAGCTGGGATTACAAGCACCTGCCACCATGCCAG TCAAGCGATTCTCCTGCCCCAGCCTCCCGAGTCGCTGGGATTACAAGCACCTGCCACCATGCCAG T G ST7L Ensembl:ENSG00000007341 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs536766496 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36720,RMVar_hsa_circ_353572,RMVar_hsa_circ_365817,RMVar_hsa_circ_135317,RMVar_hsa_circ_350204,RMVar_hsa_circ_29477,RMVar_hsa_circ_355430,RMVar_hsa_circ_88968,RMVar_hsa_circ_135325,RMVar_hsa_circ_135326,RMVar_hsa_circ_345948,RMVar_hsa_circ_293455,RMVar_hsa_circ_135330,RMVar_hsa_circ_317717,RMVar_hsa_circ_288682,RMVar_hsa_circ_135331,RMVar_hsa_circ_135332,RMVar_hsa_circ_368356,RMVar_hsa_circ_287047,RMVar_hsa_circ_318479,RMVar_hsa_circ_38754,RMVar_hsa_circ_135343,RMVar_hsa_circ_135344,RMVar_hsa_circ_347369,RMVar_hsa_circ_358887,RMVar_hsa_circ_292444,RMVar_hsa_circ_312601,RMVar_hsa_circ_270336,RMVar_hsa_circ_135352,RMVar_hsa_circ_286925,RMVar_hsa_circ_135345,RMVar_hsa_circ_135346,RMVar_hsa_circ_291467,RMVar_hsa_circ_339234,RMVar_hsa_circ_77765,RMVar_hsa_circ_135353,RMVar_hsa_circ_135355,RMVar_hsa_circ_135350,RMVar_hsa_circ_135351,RMVar_hsa_circ_354080,RMVar_hsa_circ_340249,RMVar_hsa_circ_135354 15832 RMVar_ID_15832 Human_SNP_ID_28074886 A-to-I Human chr1 - 112611781 112611781 112611781 ATTTTTATATTTTTCTGTAGAGATGAGGTCTCACTGTTTTGTCCAGGCTGGTCTAGAATTCTTGG ATTTTTATATTTTTCTGTAGAGATGAGGTCTCCCTGTTTTGTCCAGGCTGGTCTAGAATTCTTGG T G ST7L Ensembl:ENSG00000007341 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs767749001 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_286,RMVar_hsa_circ_353572,RMVar_hsa_circ_135317,RMVar_hsa_circ_350204,RMVar_hsa_circ_355430,RMVar_hsa_circ_88968,RMVar_hsa_circ_135326,RMVar_hsa_circ_293455,RMVar_hsa_circ_135330,RMVar_hsa_circ_288682,RMVar_hsa_circ_135331,RMVar_hsa_circ_368356,RMVar_hsa_circ_318479,RMVar_hsa_circ_38754,RMVar_hsa_circ_135344,RMVar_hsa_circ_347369,RMVar_hsa_circ_358887,RMVar_hsa_circ_292444,RMVar_hsa_circ_270336,RMVar_hsa_circ_135352,RMVar_hsa_circ_286925,RMVar_hsa_circ_135345,RMVar_hsa_circ_339234,RMVar_hsa_circ_77765,RMVar_hsa_circ_135353,RMVar_hsa_circ_135355,RMVar_hsa_circ_135351,RMVar_hsa_circ_354080,RMVar_hsa_circ_368927,RMVar_hsa_circ_271612,RMVar_hsa_circ_135357 15833 RMVar_ID_15833 Human_SNP_ID_28074900 A-to-I Human chr1 - 112611868 112611868 112611868 CCTCCTTGGGCTCAAGAGATCCTCCCACTTCAACTTCCTGAGTAGCTGGAACTGCAGGCATGCAC CCTCCTTGGGCTCAAGAGATCCTCCCACTTCAGCTTCCTGAGTAGCTGGAACTGCAGGCATGCAC T C ST7L Ensembl:ENSG00000007341 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs933661533 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_286,RMVar_hsa_circ_353572,RMVar_hsa_circ_135317,RMVar_hsa_circ_350204,RMVar_hsa_circ_355430,RMVar_hsa_circ_88968,RMVar_hsa_circ_135326,RMVar_hsa_circ_293455,RMVar_hsa_circ_135330,RMVar_hsa_circ_288682,RMVar_hsa_circ_135331,RMVar_hsa_circ_368356,RMVar_hsa_circ_318479,RMVar_hsa_circ_38754,RMVar_hsa_circ_135344,RMVar_hsa_circ_347369,RMVar_hsa_circ_358887,RMVar_hsa_circ_292444,RMVar_hsa_circ_270336,RMVar_hsa_circ_135352,RMVar_hsa_circ_286925,RMVar_hsa_circ_135345,RMVar_hsa_circ_339234,RMVar_hsa_circ_77765,RMVar_hsa_circ_135353,RMVar_hsa_circ_135355,RMVar_hsa_circ_135351,RMVar_hsa_circ_354080,RMVar_hsa_circ_368927,RMVar_hsa_circ_271612,RMVar_hsa_circ_135357 15834 RMVar_ID_15834 Human_SNP_ID_28074901 A-to-I Human chr1 - 112611868 112611868 112611868 CCTCCTTGGGCTCAAGAGATCCTCCCACTTCAACTTCCTGAGTAGCTGGAACTGCAGGCATGCAC CCTCCTTGGGCTCAAGAGATCCTCCCACTTCACCTTCCTGAGTAGCTGGAACTGCAGGCATGCAC T G ST7L Ensembl:ENSG00000007341 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs933661533 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_286,RMVar_hsa_circ_353572,RMVar_hsa_circ_135317,RMVar_hsa_circ_350204,RMVar_hsa_circ_355430,RMVar_hsa_circ_88968,RMVar_hsa_circ_135326,RMVar_hsa_circ_293455,RMVar_hsa_circ_135330,RMVar_hsa_circ_288682,RMVar_hsa_circ_135331,RMVar_hsa_circ_368356,RMVar_hsa_circ_318479,RMVar_hsa_circ_38754,RMVar_hsa_circ_135344,RMVar_hsa_circ_347369,RMVar_hsa_circ_358887,RMVar_hsa_circ_292444,RMVar_hsa_circ_270336,RMVar_hsa_circ_135352,RMVar_hsa_circ_286925,RMVar_hsa_circ_135345,RMVar_hsa_circ_339234,RMVar_hsa_circ_77765,RMVar_hsa_circ_135353,RMVar_hsa_circ_135355,RMVar_hsa_circ_135351,RMVar_hsa_circ_354080,RMVar_hsa_circ_368927,RMVar_hsa_circ_271612,RMVar_hsa_circ_135357 15835 RMVar_ID_15835 Human_SNP_ID_28075148 A-to-I Human chr1 - 112612855 112612855 112612855 CCTCAGCCTCCCAAAGTGTTGGGATTATAGGCATGAGCCACCGTGCCTGGCCCTATCCAATTTTC CCTCAGCCTCCCAAAGTGTTGGGATTATAGGCGTGAGCCACCGTGCCTGGCCCTATCCAATTTTC T C ST7L Ensembl:ENSG00000007341 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs376192491 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_220946 RMVar_hsa_circ_286,RMVar_hsa_circ_353572,RMVar_hsa_circ_135317,RMVar_hsa_circ_350204,RMVar_hsa_circ_355430,RMVar_hsa_circ_88968,RMVar_hsa_circ_135326,RMVar_hsa_circ_293455,RMVar_hsa_circ_135330,RMVar_hsa_circ_288682,RMVar_hsa_circ_135331,RMVar_hsa_circ_368356,RMVar_hsa_circ_318479,RMVar_hsa_circ_38754,RMVar_hsa_circ_135344,RMVar_hsa_circ_347369,RMVar_hsa_circ_358887,RMVar_hsa_circ_292444,RMVar_hsa_circ_270336,RMVar_hsa_circ_135352,RMVar_hsa_circ_286925,RMVar_hsa_circ_135345,RMVar_hsa_circ_339234,RMVar_hsa_circ_77765,RMVar_hsa_circ_135353,RMVar_hsa_circ_135355,RMVar_hsa_circ_135351,RMVar_hsa_circ_354080,RMVar_hsa_circ_368927,RMVar_hsa_circ_271612,RMVar_hsa_circ_135357 15836 RMVar_ID_15836 Human_SNP_ID_28075363 A-to-I Human chr1 - 112613866 112613866 112613866 AAATTTAGCGCGTTGTGGTGGCGCATTCCTGTAGTCCCAGCTACTTCAGAGACTGAGGTGGGAGG AAATTTAGCGCGTTGTGGTGGCGCATTCCTGTGGTCCCAGCTACTTCAGAGACTGAGGTGGGAGG T C ST7L Ensembl:ENSG00000007341 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs541658934 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_286,RMVar_hsa_circ_353572,RMVar_hsa_circ_135317,RMVar_hsa_circ_350204,RMVar_hsa_circ_355430,RMVar_hsa_circ_88968,RMVar_hsa_circ_135326,RMVar_hsa_circ_293455,RMVar_hsa_circ_135330,RMVar_hsa_circ_288682,RMVar_hsa_circ_135331,RMVar_hsa_circ_368356,RMVar_hsa_circ_318479,RMVar_hsa_circ_38754,RMVar_hsa_circ_135344,RMVar_hsa_circ_347369,RMVar_hsa_circ_358887,RMVar_hsa_circ_292444,RMVar_hsa_circ_270336,RMVar_hsa_circ_135352,RMVar_hsa_circ_286925,RMVar_hsa_circ_135345,RMVar_hsa_circ_339234,RMVar_hsa_circ_77765,RMVar_hsa_circ_135353,RMVar_hsa_circ_135355,RMVar_hsa_circ_135351,RMVar_hsa_circ_354080,RMVar_hsa_circ_368927,RMVar_hsa_circ_271612,RMVar_hsa_circ_135357 15837 RMVar_ID_15837 Human_SNP_ID_28075811 A-to-I Human chr1 - 112615878 112615878 112615878 AAAAATAACTGGGTATGGTGGTATGTGCCTGTAGTCCCAGCTACTCGGAAGGCTGAGGCATAAGA AAAAATAACTGGGTATGGTGGTATGTGCCTGTGGTCCCAGCTACTCGGAAGGCTGAGGCATAAGA T C ST7L Ensembl:ENSG00000007341 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1237499897 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_286,RMVar_hsa_circ_353572,RMVar_hsa_circ_135317,RMVar_hsa_circ_350204,RMVar_hsa_circ_355430,RMVar_hsa_circ_88968,RMVar_hsa_circ_135326,RMVar_hsa_circ_293455,RMVar_hsa_circ_135330,RMVar_hsa_circ_288682,RMVar_hsa_circ_135331,RMVar_hsa_circ_368356,RMVar_hsa_circ_318479,RMVar_hsa_circ_38754,RMVar_hsa_circ_135344,RMVar_hsa_circ_347369,RMVar_hsa_circ_358887,RMVar_hsa_circ_292444,RMVar_hsa_circ_270336,RMVar_hsa_circ_135352,RMVar_hsa_circ_286925,RMVar_hsa_circ_135345,RMVar_hsa_circ_339234,RMVar_hsa_circ_77765,RMVar_hsa_circ_135353,RMVar_hsa_circ_135355,RMVar_hsa_circ_135351,RMVar_hsa_circ_354080,RMVar_hsa_circ_368927,RMVar_hsa_circ_271612,RMVar_hsa_circ_135357 15838 RMVar_ID_15838 Human_SNP_ID_28077957 A-to-I Human chr1 + 112623633 112623633 112623633 AACCTGGGAGGCGGAGGTTGCGGTGACCCGAGATCACGCCATTGCACTCCAGCCTGGGCAACAGG AACCTGGGAGGCGGAGGTTGCGGTGACCCGAGGTCACGCCATTGCACTCCAGCCTGGGCAACAGG A G CAPZA1 Ensembl:ENSG00000116489 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs541590247 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101246,RMVar_hsa_circ_114420,RMVar_hsa_circ_135359,RMVar_hsa_circ_135360 15839 RMVar_ID_15839 Human_SNP_ID_28081035 A-to-I Human chr1 + 112637484 112637484 112637484 TTTTGTTGTTTGTTGAGACAGGCTCTTGCTCTATTGCACAGGCTGGAGTGCAGTGGCACAATCAT TTTTGTTGTTTGTTGAGACAGGCTCTTGCTCTGTTGCACAGGCTGGAGTGCAGTGGCACAATCAT A G CAPZA1 Ensembl:ENSG00000116489 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs554196626 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101246,RMVar_hsa_circ_114420,RMVar_hsa_circ_135359,RMVar_hsa_circ_135360 15840 RMVar_ID_15840 Human_SNP_ID_28085530 A-to-I Human chr1 + 112655366 112655366 112655366 GGATGTGGTGGTGCACACCTGTAGTTTCAGCTACTCAGGAGGCTGAGGCACAAGAATCACTTGAA GGATGTGGTGGTGCACACCTGTAGTTTCAGCTGCTCAGGAGGCTGAGGCACAAGAATCACTTGAA A G CAPZA1 Ensembl:ENSG00000116489 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs947720229 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101246,RMVar_hsa_circ_114420,RMVar_hsa_circ_79195,RMVar_hsa_circ_135359,RMVar_hsa_circ_135360,RMVar_hsa_circ_115871,RMVar_hsa_circ_321618,RMVar_hsa_circ_64257,RMVar_hsa_circ_135361,RMVar_hsa_circ_135362,RMVar_hsa_circ_135363,RMVar_hsa_circ_135364,RMVar_hsa_circ_371272,RMVar_hsa_circ_374167,RMVar_hsa_circ_283831,RMVar_hsa_circ_284667,RMVar_hsa_circ_84634,RMVar_hsa_circ_119207,RMVar_hsa_circ_135368,RMVar_hsa_circ_135370,RMVar_hsa_circ_75602,RMVar_hsa_circ_135371,RMVar_hsa_circ_135369,RMVar_hsa_circ_135367,RMVar_hsa_circ_335980,RMVar_hsa_circ_135372 15841 RMVar_ID_15841 Human_SNP_ID_28087187 A-to-I Human chr1 + 112662209 112662209 112662209 ATAGCTCACTGCAACCTCAAACTCCTCAACTAAATGATCCTCCCACCTCATCCTCCCAAGCACCT ATAGCTCACTGCAACCTCAAACTCCTCAACTACATGATCCTCCCACCTCATCCTCCCAAGCACCT A C CAPZA1 Ensembl:ENSG00000116489 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1454595388 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23302726 RMVar_hsa_circ_101246,RMVar_hsa_circ_79195,RMVar_hsa_circ_135359,RMVar_hsa_circ_115871,RMVar_hsa_circ_64257,RMVar_hsa_circ_135362,RMVar_hsa_circ_135363,RMVar_hsa_circ_374167,RMVar_hsa_circ_284667,RMVar_hsa_circ_119207,RMVar_hsa_circ_135370,RMVar_hsa_circ_75602,RMVar_hsa_circ_135371,RMVar_hsa_circ_135369,RMVar_hsa_circ_335980,RMVar_hsa_circ_103569,RMVar_hsa_circ_290797,RMVar_hsa_circ_135372,RMVar_hsa_circ_135373,RMVar_hsa_circ_97171,RMVar_hsa_circ_135374,RMVar_hsa_circ_321150 15842 RMVar_ID_15842 Human_SNP_ID_28087574 A-to-I Human chr1 + 112663571 112663571 112663571 TCACCCAGGCTGGAGTGCAGTGGTGCAATCTCAGTTCACTGCAGCCTCTGCCTCCTGGCTTCAAG TCACCCAGGCTGGAGTGCAGTGGTGCAATCTCGGTTCACTGCAGCCTCTGCCTCCTGGCTTCAAG A G CAPZA1 Ensembl:ENSG00000116489 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1336459763 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101246,RMVar_hsa_circ_79195,RMVar_hsa_circ_135359,RMVar_hsa_circ_115871,RMVar_hsa_circ_64257,RMVar_hsa_circ_135362,RMVar_hsa_circ_135363,RMVar_hsa_circ_374167,RMVar_hsa_circ_284667,RMVar_hsa_circ_119207,RMVar_hsa_circ_135370,RMVar_hsa_circ_75602,RMVar_hsa_circ_135371,RMVar_hsa_circ_135369,RMVar_hsa_circ_335980,RMVar_hsa_circ_103569,RMVar_hsa_circ_290797,RMVar_hsa_circ_135372,RMVar_hsa_circ_135373,RMVar_hsa_circ_97171,RMVar_hsa_circ_135374,RMVar_hsa_circ_321150 15843 RMVar_ID_15843 Human_SNP_ID_28087600 A-to-I Human chr1 + 112663705 112663705 112663705 TTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGTCAGGCTGGTCTCGAACTCCTGACCT TTTTGTATTTTTAGTAGAGACAGGGTTTCACCGTGTTGGTCAGGCTGGTCTCGAACTCCTGACCT A G CAPZA1 Ensembl:ENSG00000116489 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1294364598 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101246,RMVar_hsa_circ_79195,RMVar_hsa_circ_135359,RMVar_hsa_circ_115871,RMVar_hsa_circ_64257,RMVar_hsa_circ_135362,RMVar_hsa_circ_135363,RMVar_hsa_circ_374167,RMVar_hsa_circ_284667,RMVar_hsa_circ_119207,RMVar_hsa_circ_135370,RMVar_hsa_circ_75602,RMVar_hsa_circ_135371,RMVar_hsa_circ_135369,RMVar_hsa_circ_335980,RMVar_hsa_circ_103569,RMVar_hsa_circ_290797,RMVar_hsa_circ_135372,RMVar_hsa_circ_135373,RMVar_hsa_circ_97171,RMVar_hsa_circ_135374,RMVar_hsa_circ_321150 15844 RMVar_ID_15844 Human_SNP_ID_28087601 A-to-I Human chr1 + 112663705 112663705 112663705 TTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGTCAGGCTGGTCTCGAACTCCTGACCT TTTTGTATTTTTAGTAGAGACAGGGTTTCACCTTGTTGGTCAGGCTGGTCTCGAACTCCTGACCT A T CAPZA1 Ensembl:ENSG00000116489 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1294364598 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101246,RMVar_hsa_circ_79195,RMVar_hsa_circ_135359,RMVar_hsa_circ_115871,RMVar_hsa_circ_64257,RMVar_hsa_circ_135362,RMVar_hsa_circ_135363,RMVar_hsa_circ_374167,RMVar_hsa_circ_284667,RMVar_hsa_circ_119207,RMVar_hsa_circ_135370,RMVar_hsa_circ_75602,RMVar_hsa_circ_135371,RMVar_hsa_circ_135369,RMVar_hsa_circ_335980,RMVar_hsa_circ_103569,RMVar_hsa_circ_290797,RMVar_hsa_circ_135372,RMVar_hsa_circ_135373,RMVar_hsa_circ_97171,RMVar_hsa_circ_135374,RMVar_hsa_circ_321150 15845 RMVar_ID_15845 Human_SNP_ID_28087837 A-to-I Human chr1 + 112664664 112664664 112664664 TTTTGTAAAGATTAAATGTGGTGGCCTAGCGCAGTGGCTCATGACTGTAATCCCAGTACTTTTGG TTTTGTAAAGATTAAATGTGGTGGCCTAGCGCCGTGGCTCATGACTGTAATCCCAGTACTTTTGG A C CAPZA1 Ensembl:ENSG00000116489 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559007929 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101246,RMVar_hsa_circ_79195,RMVar_hsa_circ_135359,RMVar_hsa_circ_115871,RMVar_hsa_circ_64257,RMVar_hsa_circ_135362,RMVar_hsa_circ_135363,RMVar_hsa_circ_374167,RMVar_hsa_circ_284667,RMVar_hsa_circ_119207,RMVar_hsa_circ_135370,RMVar_hsa_circ_75602,RMVar_hsa_circ_135371,RMVar_hsa_circ_135369,RMVar_hsa_circ_335980,RMVar_hsa_circ_103569,RMVar_hsa_circ_290797,RMVar_hsa_circ_135372,RMVar_hsa_circ_135373,RMVar_hsa_circ_97171,RMVar_hsa_circ_135374,RMVar_hsa_circ_321150 15846 RMVar_ID_15846 Human_SNP_ID_28087838 A-to-I Human chr1 + 112664664 112664664 112664664 TTTTGTAAAGATTAAATGTGGTGGCCTAGCGCAGTGGCTCATGACTGTAATCCCAGTACTTTTGG TTTTGTAAAGATTAAATGTGGTGGCCTAGCGCGGTGGCTCATGACTGTAATCCCAGTACTTTTGG A G CAPZA1 Ensembl:ENSG00000116489 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559007929 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101246,RMVar_hsa_circ_79195,RMVar_hsa_circ_135359,RMVar_hsa_circ_115871,RMVar_hsa_circ_64257,RMVar_hsa_circ_135362,RMVar_hsa_circ_135363,RMVar_hsa_circ_374167,RMVar_hsa_circ_284667,RMVar_hsa_circ_119207,RMVar_hsa_circ_135370,RMVar_hsa_circ_75602,RMVar_hsa_circ_135371,RMVar_hsa_circ_135369,RMVar_hsa_circ_335980,RMVar_hsa_circ_103569,RMVar_hsa_circ_290797,RMVar_hsa_circ_135372,RMVar_hsa_circ_135373,RMVar_hsa_circ_97171,RMVar_hsa_circ_135374,RMVar_hsa_circ_321150 15847 RMVar_ID_15847 Human_SNP_ID_28087839 A-to-I Human chr1 + 112664664 112664664 112664664 TTTTGTAAAGATTAAATGTGGTGGCCTAGCGCAGTGGCTCATGACTGTAATCCCAGTACTTTTGG TTTTGTAAAGATTAAATGTGGTGGCCTAGCGCTGTGGCTCATGACTGTAATCCCAGTACTTTTGG A T CAPZA1 Ensembl:ENSG00000116489 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559007929 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101246,RMVar_hsa_circ_79195,RMVar_hsa_circ_135359,RMVar_hsa_circ_115871,RMVar_hsa_circ_64257,RMVar_hsa_circ_135362,RMVar_hsa_circ_135363,RMVar_hsa_circ_374167,RMVar_hsa_circ_284667,RMVar_hsa_circ_119207,RMVar_hsa_circ_135370,RMVar_hsa_circ_75602,RMVar_hsa_circ_135371,RMVar_hsa_circ_135369,RMVar_hsa_circ_335980,RMVar_hsa_circ_103569,RMVar_hsa_circ_290797,RMVar_hsa_circ_135372,RMVar_hsa_circ_135373,RMVar_hsa_circ_97171,RMVar_hsa_circ_135374,RMVar_hsa_circ_321150 15848 RMVar_ID_15848 Human_SNP_ID_28087855 A-to-I Human chr1 + 112664725 112664725 112664725 TTGGGAGACCGAGGTGGGTGGATCACAAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGA TTGGGAGACCGAGGTGGGTGGATCACAAGGTCGGGAGTTCGAGACCAGCCTGGCCAACATGGTGA A G CAPZA1 Ensembl:ENSG00000116489 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1185603098 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101246,RMVar_hsa_circ_79195,RMVar_hsa_circ_135359,RMVar_hsa_circ_115871,RMVar_hsa_circ_64257,RMVar_hsa_circ_135362,RMVar_hsa_circ_135363,RMVar_hsa_circ_374167,RMVar_hsa_circ_284667,RMVar_hsa_circ_119207,RMVar_hsa_circ_135370,RMVar_hsa_circ_75602,RMVar_hsa_circ_135371,RMVar_hsa_circ_135369,RMVar_hsa_circ_335980,RMVar_hsa_circ_103569,RMVar_hsa_circ_290797,RMVar_hsa_circ_135372,RMVar_hsa_circ_135373,RMVar_hsa_circ_97171,RMVar_hsa_circ_135374,RMVar_hsa_circ_321150 15849 RMVar_ID_15849 Human_SNP_ID_28087862 A-to-I Human chr1 + 112664758 112664758 112664758 GGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCTCGTCTCTACTAAAAATACAAAAGTTAGC GGAGTTCGAGACCAGCCTGGCCAACATGGTGATACCTCGTCTCTACTAAAAATACAAAAGTTAGC A T CAPZA1 Ensembl:ENSG00000116489 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs575871756 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101246,RMVar_hsa_circ_79195,RMVar_hsa_circ_135359,RMVar_hsa_circ_115871,RMVar_hsa_circ_64257,RMVar_hsa_circ_135362,RMVar_hsa_circ_135363,RMVar_hsa_circ_374167,RMVar_hsa_circ_284667,RMVar_hsa_circ_119207,RMVar_hsa_circ_135370,RMVar_hsa_circ_75602,RMVar_hsa_circ_135371,RMVar_hsa_circ_135369,RMVar_hsa_circ_335980,RMVar_hsa_circ_103569,RMVar_hsa_circ_290797,RMVar_hsa_circ_135372,RMVar_hsa_circ_135373,RMVar_hsa_circ_97171,RMVar_hsa_circ_135374,RMVar_hsa_circ_321150 15850 RMVar_ID_15850 Human_SNP_ID_28088503 A-to-I Human chr1 + 112667638 112667638 112667638 TCACTGCAGCCTTGAGCTCCCAGGCTCAAGCGATCCTCCCACCTCAGCCTCCCAAGTAGCTGGGA TCACTGCAGCCTTGAGCTCCCAGGCTCAAGCGGTCCTCCCACCTCAGCCTCCCAAGTAGCTGGGA A G CAPZA1 Ensembl:ENSG00000116489 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs143600243 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101246,RMVar_hsa_circ_79195,RMVar_hsa_circ_135359,RMVar_hsa_circ_115871,RMVar_hsa_circ_135362,RMVar_hsa_circ_135363,RMVar_hsa_circ_374167,RMVar_hsa_circ_46452,RMVar_hsa_circ_119207,RMVar_hsa_circ_135370,RMVar_hsa_circ_75602,RMVar_hsa_circ_135371,RMVar_hsa_circ_335980,RMVar_hsa_circ_103569,RMVar_hsa_circ_135372,RMVar_hsa_circ_135373,RMVar_hsa_circ_97171,RMVar_hsa_circ_135374,RMVar_hsa_circ_117493,RMVar_hsa_circ_321150,RMVar_hsa_circ_135376 15851 RMVar_ID_15851 Human_SNP_ID_28088511 A-to-I Human chr1 + 112667699 112667699 112667699 GGGACCACAGGTGCATGCCACCATGCCCAGCTAATTTTTTTATTTTTGGTAGAGATGAGGTTTCT GGGACCACAGGTGCATGCCACCATGCCCAGCTCATTTTTTTATTTTTGGTAGAGATGAGGTTTCT A C CAPZA1 Ensembl:ENSG00000116489 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1457983583 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101246,RMVar_hsa_circ_79195,RMVar_hsa_circ_135359,RMVar_hsa_circ_115871,RMVar_hsa_circ_135362,RMVar_hsa_circ_135363,RMVar_hsa_circ_374167,RMVar_hsa_circ_46452,RMVar_hsa_circ_119207,RMVar_hsa_circ_135370,RMVar_hsa_circ_75602,RMVar_hsa_circ_135371,RMVar_hsa_circ_335980,RMVar_hsa_circ_103569,RMVar_hsa_circ_135372,RMVar_hsa_circ_135373,RMVar_hsa_circ_97171,RMVar_hsa_circ_135374,RMVar_hsa_circ_117493,RMVar_hsa_circ_321150,RMVar_hsa_circ_135376 15852 RMVar_ID_15852 Human_SNP_ID_28094138 A-to-I Human chr1 + 112691230 112691230 112691230 TTGCTTGAACCTGGGAGGCGGTGGTTGCAGTGAGCCGAGATTGCGCCATTGCACTTCAGCCTGGG TTGCTTGAACCTGGGAGGCGGTGGTTGCAGTGCGCCGAGATTGCGCCATTGCACTTCAGCCTGGG A C MOV10 Ensembl:ENSG00000155363 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1195799294 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81633,RMVar_hsa_circ_135378 15853 RMVar_ID_15853 Human_SNP_ID_28097103 A-to-I Human chr1 - 112701328 112701328 112701328 CTGGGAGCCACGCCTATGCCCTGCCCTTCCTCAGGGCCCCTGGGGATCTTGCCCCCTTTGACCTT CTGGGAGCCACGCCTATGCCCTGCCCTTCCTCGGGGCCCCTGGGGATCTTGCCCCCTTTGACCTT T C RHOC Ensembl:ENSG00000155366 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs887825672 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5108708,Human_RBP_ID_17647031,Human_RBP_ID_18187208,Human_RBP_ID_27554177 Human_miRNA_ID_97539,Human_miRNA_ID_118583,Human_miRNA_ID_122391,Human_miRNA_ID_863803,Human_miRNA_ID_1972059,Human_miRNA_ID_1972060,Human_miRNA_ID_1974237,Human_miRNA_ID_1974238,Human_miRNA_ID_2256009,Human_miRNA_ID_2256010,Human_miRNA_ID_2612063,Human_miRNA_ID_2612064 RMVar_hsa_circ_110082,RMVar_hsa_circ_124770,RMVar_hsa_circ_126300,RMVar_hsa_circ_112194,RMVar_hsa_circ_135387,RMVar_hsa_circ_103000,RMVar_hsa_circ_104408,RMVar_hsa_circ_135389,RMVar_hsa_circ_84742,RMVar_hsa_circ_135390,RMVar_hsa_circ_135388,RMVar_hsa_circ_135385,RMVar_hsa_circ_135386,RMVar_hsa_circ_135384 15854 RMVar_ID_15854 Human_SNP_ID_28097104 A-to-I Human chr1 - 112701328 112701328 112701328 CTGGGAGCCACGCCTATGCCCTGCCCTTCCTCAGGGCCCCTGGGGATCTTGCCCCCTTTGACCTT CTGGGAGCCACGCCTATGCCCTGCCCTTCCTCCGGGCCCCTGGGGATCTTGCCCCCTTTGACCTT T G RHOC Ensembl:ENSG00000155366 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs887825672 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5108708,Human_RBP_ID_17647031,Human_RBP_ID_18187208,Human_RBP_ID_27554177 Human_miRNA_ID_97539,Human_miRNA_ID_118583,Human_miRNA_ID_122391,Human_miRNA_ID_863803,Human_miRNA_ID_1972059,Human_miRNA_ID_1972060,Human_miRNA_ID_1974237,Human_miRNA_ID_1974238,Human_miRNA_ID_2256009,Human_miRNA_ID_2256010,Human_miRNA_ID_2612063,Human_miRNA_ID_2612064 RMVar_hsa_circ_110082,RMVar_hsa_circ_124770,RMVar_hsa_circ_126300,RMVar_hsa_circ_112194,RMVar_hsa_circ_135387,RMVar_hsa_circ_103000,RMVar_hsa_circ_104408,RMVar_hsa_circ_135389,RMVar_hsa_circ_84742,RMVar_hsa_circ_135390,RMVar_hsa_circ_135388,RMVar_hsa_circ_135385,RMVar_hsa_circ_135386,RMVar_hsa_circ_135384 15855 RMVar_ID_15855 Human_SNP_ID_28117499 A-to-I Human chr1 + 112776299 112776299 112776299 TCAAGCGATTCTCCTGCCTCAGCCTCCTCAGTAGCTGGGATTGCGGGCACCTGCCACCATGCCCA TCAAGCGATTCTCCTGCCTCAGCCTCCTCAGTGGCTGGGATTGCGGGCACCTGCCACCATGCCCA A G lnc-FAM19A3-6,lnc-FAM19A3-6:2 RNACentral:URS0000E3791C,RNACentral:URS0000D57B87 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1016579494 Functional Loss SNV dbSNP153 33..33 33 - - - 15856 RMVar_ID_15856 Human_SNP_ID_28157596 A-to-I Human chr1 - 112922699 112922699 112922699 GCAATCTTGGCTCACTGCAACCTCCACCTCCCAGGTTCAAGCCATTCTCCTGCCTCAGCCTTCGG GCAATCTTGGCTCACTGCAACCTCCACCTCCCGGGTTCAAGCCATTCTCCTGCCTCAGCCTTCGG T C SLC16A1 Ensembl:ENSG00000155380 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs961641632 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_135398,RMVar_hsa_circ_294281,RMVar_hsa_circ_135400,RMVar_hsa_circ_309010 15857 RMVar_ID_15857 Human_SNP_ID_28157613 A-to-I Human chr1 - 112922756 112922756 112922756 TTTGTTTGTTTTTTGAGACAGAGTCTCACTCTATTGCCCAGGCTGGAGTGCAGTGGCGCAATCTT TTTGTTTGTTTTTTGAGACAGAGTCTCACTCTGTTGCCCAGGCTGGAGTGCAGTGGCGCAATCTT T C SLC16A1 Ensembl:ENSG00000155380 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs984916585 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_135398,RMVar_hsa_circ_294281,RMVar_hsa_circ_135400,RMVar_hsa_circ_309010 15858 RMVar_ID_15858 Human_SNP_ID_28157960 A-to-I Human chr1 + 112923982 112923982 112923982 CTGGGGACCTGCTGACTGGCAAGTACAAGTATAAGGACAAGGACAGGAAACAGCCCATGGGCCGC CTGGGGACCTGCTGACTGGCAAGTACAAGTATGAGGACAAGGACAGGAAACAGCCCATGGGCCGC A G AKR7A2P1 Ensembl:ENSG00000229020 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878997976 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1844304 RMVar_hsa_circ_265530 15859 RMVar_ID_15859 Human_SNP_ID_28158384 A-to-I Human chr1 - 112925611 112925611 112925611 ACTTTGGGAGGCCTAGGTAGGTGGATCACTTGAGTCCGGGATTACAAGACCAACCTGGGCAACAT ACTTTGGGAGGCCTAGGTAGGTGGATCACTTGGGTCCGGGATTACAAGACCAACCTGGGCAACAT T C SLC16A1 Ensembl:ENSG00000155380 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs577249995 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_135398,RMVar_hsa_circ_294281,RMVar_hsa_circ_135400,RMVar_hsa_circ_309010 15860 RMVar_ID_15860 Human_SNP_ID_28158385 A-to-I Human chr1 - 112925611 112925611 112925611 ACTTTGGGAGGCCTAGGTAGGTGGATCACTTGAGTCCGGGATTACAAGACCAACCTGGGCAACAT ACTTTGGGAGGCCTAGGTAGGTGGATCACTTGCGTCCGGGATTACAAGACCAACCTGGGCAACAT T G SLC16A1 Ensembl:ENSG00000155380 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs577249995 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_135398,RMVar_hsa_circ_294281,RMVar_hsa_circ_135400,RMVar_hsa_circ_309010 15861 RMVar_ID_15861 Human_SNP_ID_28158392 A-to-I Human chr1 - 112925654 112925654 112925654 GAAGAGAAGGCCAGGCACGGTGGCTCACACCTATAATCCCAGCACTTTGGGAGGCCTAGGTAGGT GAAGAGAAGGCCAGGCACGGTGGCTCACACCTTTAATCCCAGCACTTTGGGAGGCCTAGGTAGGT T A SLC16A1 Ensembl:ENSG00000155380 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs945307433 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24573597 RMVar_hsa_circ_135398,RMVar_hsa_circ_294281,RMVar_hsa_circ_135400,RMVar_hsa_circ_309010 15862 RMVar_ID_15862 Human_SNP_ID_28158393 A-to-I Human chr1 - 112925654 112925654 112925654 GAAGAGAAGGCCAGGCACGGTGGCTCACACCTATAATCCCAGCACTTTGGGAGGCCTAGGTAGGT GAAGAGAAGGCCAGGCACGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCTAGGTAGGT T C SLC16A1 Ensembl:ENSG00000155380 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs945307433 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24573597 RMVar_hsa_circ_135398,RMVar_hsa_circ_294281,RMVar_hsa_circ_135400,RMVar_hsa_circ_309010 15863 RMVar_ID_15863 Human_SNP_ID_28167418 A-to-I Human chr1 + 112961929 112961929 112961929 TGCTGGGAAAATTGGAAAGTCACATGCAGAAGAATAAGACTAGACCCTGTCTCCACCATATACAC TGCTGGGAAAATTGGAAAGTCACATGCAGAAGGATAAGACTAGACCCTGTCTCCACCATATACAC A G SLC16A1-AS1 Ensembl:ENSG00000226419 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs748000137 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5245185,Human_RBP_ID_8241739,Human_RBP_ID_10526654 RMVar_hsa_circ_35397,RMVar_hsa_circ_135403 15864 RMVar_ID_15864 Human_SNP_ID_28167431 A-to-I Human chr1 + 112961963 112961963 112961963 TAAGACTAGACCCTGTCTCCACCATATACACAAATCAACTCAAAATGGATTAAAGACTGTCTTCT TAAGACTAGACCCTGTCTCCACCATATACACAGATCAACTCAAAATGGATTAAAGACTGTCTTCT A G SLC16A1-AS1 Ensembl:ENSG00000226419 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs190341134 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5245186,Human_RBP_ID_5672509,Human_RBP_ID_8241739,Human_RBP_ID_9554182,Human_RBP_ID_17721660,Human_RBP_ID_23260080,Human_RBP_ID_24750423 RMVar_hsa_circ_35397,RMVar_hsa_circ_135403 15865 RMVar_ID_15865 Human_SNP_ID_28167657 A-to-I Human chr1 + 112963088 112963088 112963088 AAGTCTTTAATCCATTTTGAGTTGATTTGTGTATATAGTGGAGACAGGGTCTAGTCTTAGTCTTC AAGTCTTTAATCCATTTTGAGTTGATTTGTGTGTATAGTGGAGACAGGGTCTAGTCTTAGTCTTC A G SLC16A1-AS1 Ensembl:ENSG00000226419 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1343355758 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23323822 RMVar_hsa_circ_35397,RMVar_hsa_circ_135403 15866 RMVar_ID_15866 Human_SNP_ID_28167659 A-to-I Human chr1 + 112963092 112963092 112963092 CTTTAATCCATTTTGAGTTGATTTGTGTATATAGTGGAGACAGGGTCTAGTCTTAGTCTTCTGCA CTTTAATCCATTTTGAGTTGATTTGTGTATATCGTGGAGACAGGGTCTAGTCTTAGTCTTCTGCA A C SLC16A1-AS1 Ensembl:ENSG00000226419 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs981414357 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23323822 RMVar_hsa_circ_35397,RMVar_hsa_circ_135403 15867 RMVar_ID_15867 Human_SNP_ID_28167660 A-to-I Human chr1 + 112963092 112963092 112963092 CTTTAATCCATTTTGAGTTGATTTGTGTATATAGTGGAGACAGGGTCTAGTCTTAGTCTTCTGCA CTTTAATCCATTTTGAGTTGATTTGTGTATATGGTGGAGACAGGGTCTAGTCTTAGTCTTCTGCA A G SLC16A1-AS1 Ensembl:ENSG00000226419 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs981414357 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23323822 RMVar_hsa_circ_35397,RMVar_hsa_circ_135403 15868 RMVar_ID_15868 Human_SNP_ID_28168391 A-to-I Human chr1 + 112965777 112965777 112965777 GCGATTTTGGCGCACTGCAAGCTCGGCCTCCCAGGTTCACGCCACTCTCCTGCCTCAGCCTCCTG GCGATTTTGGCGCACTGCAAGCTCGGCCTCCCGGGTTCACGCCACTCTCCTGCCTCAGCCTCCTG A G SLC16A1-AS1 Ensembl:ENSG00000226419 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1320603677 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10526747 RMVar_hsa_circ_35397,RMVar_hsa_circ_135403 15869 RMVar_ID_15869 Human_SNP_ID_28169345 A-to-I Human chr1 + 112969572 112969571 112969572 AAAATTAGTCGGGCATGGTGGCAGGCATCTGTAATCGCAGCTACTTGGGAGGCTGAGGCAGGAGA AAAATTAGTCGGGCATGGTGGCAGGCATCTGT_ATCGCAGCTACTTGGGAGGCTGAGGCAGGAGA TA T SLC16A1-AS1 Ensembl:ENSG00000226419 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1469481585 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_35397,RMVar_hsa_circ_135403 15870 RMVar_ID_15870 Human_SNP_ID_28169357 A-to-I Human chr1 + 112969619 112969619 112969619 GGAGGCTGAGGCAGGAGAATCGCTTGAACCCCAGAGGCAGAGGTTGCAGTGAGTTGAGATCGCGT GGAGGCTGAGGCAGGAGAATCGCTTGAACCCCGGAGGCAGAGGTTGCAGTGAGTTGAGATCGCGT A G SLC16A1-AS1 Ensembl:ENSG00000226419 lincRNA exon GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1381163979 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35397,RMVar_hsa_circ_135403 15871 RMVar_ID_15871 Human_SNP_ID_28169639 A-to-I Human chr1 + 112970479 112970479 112970479 TTGGTTCACTGCAACCTCTGCCTCCCAGGTTCAAGTAATTCTCCTGCCTCAGCCTCCCCAGTAAC TTGGTTCACTGCAACCTCTGCCTCCCAGGTTCGAGTAATTCTCCTGCCTCAGCCTCCCCAGTAAC A G SLC16A1-AS1 Ensembl:ENSG00000226419 lincRNA exon GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1234502354 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35397,RMVar_hsa_circ_135403 15872 RMVar_ID_15872 Human_SNP_ID_28171678 A-to-I Human chr1 + 112979113 112979112 112979113 CCCACTGTAACCTCAAACTCCTAGGCTCAAGCAGTTCTCCCACTTCAACCTTCTGCGGGGCTAGG CCCACTGTAACCTCAAACTCCTAGGCTCAAGC_GTTCTCCCACTTCAACCTTCTGCGGGGCTAGG CA C SLC16A1-AS1 Ensembl:ENSG00000226419 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1442161527 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_35397,RMVar_hsa_circ_135403 15873 RMVar_ID_15873 Human_SNP_ID_28171687 A-to-I Human chr1 + 112979143 112979143 112979143 GCAGTTCTCCCACTTCAACCTTCTGCGGGGCTAGGACTACAGGAAGACACCACCATGCCCAGCTA GCAGTTCTCCCACTTCAACCTTCTGCGGGGCTGGGACTACAGGAAGACACCACCATGCCCAGCTA A G SLC16A1-AS1 Ensembl:ENSG00000226419 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285841069 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35397,RMVar_hsa_circ_135403 15874 RMVar_ID_15874 Human_SNP_ID_28171690 A-to-I Human chr1 + 112979149 112979149 112979149 CTCCCACTTCAACCTTCTGCGGGGCTAGGACTACAGGAAGACACCACCATGCCCAGCTAATTTTT CTCCCACTTCAACCTTCTGCGGGGCTAGGACTGCAGGAAGACACCACCATGCCCAGCTAATTTTT A G SLC16A1-AS1 Ensembl:ENSG00000226419 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1332017455 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35397,RMVar_hsa_circ_135403 15875 RMVar_ID_15875 Human_SNP_ID_28172916 A-to-I Human chr1 + 112984432 112984432 112984432 ACAGGGTCTCACTGTGTGGCCCAGGCTGGAGTACAGTGGCGCGATCTCGGCTCACTGCAACCTCC ACAGGGTCTCACTGTGTGGCCCAGGCTGGAGTGCAGTGGCGCGATCTCGGCTCACTGCAACCTCC A G SLC16A1-AS1 Ensembl:ENSG00000226419 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs564216437 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35397,RMVar_hsa_circ_135403 15876 RMVar_ID_15876 Human_SNP_ID_28176997 A-to-I Human chr1 + 113001695 113001695 113001695 CACCGCGCCCGGCCTGGAACTCCTGACTTTATAATCCACCTGCCTTGCCTCCCAAAGTGCTGAGA CACCGCGCCCGGCCTGGAACTCCTGACTTTATGATCCACCTGCCTTGCCTCCCAAAGTGCTGAGA A G SLC16A1-AS1 Ensembl:ENSG00000226419 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1214601550 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35397,RMVar_hsa_circ_135404,RMVar_hsa_circ_338255 15877 RMVar_ID_15877 Human_SNP_ID_28177376 A-to-I Human chr1 + 113003536 113003536 113003536 TATCATGCCCAACTAAGTTTTGTATTTTTAGTAGGGACGGGGTTTCACTGTGCTAGCCAGGATGG TATCATGCCCAACTAAGTTTTGTATTTTTAGTGGGGACGGGGTTTCACTGTGCTAGCCAGGATGG A G SLC16A1-AS1 Ensembl:ENSG00000226419 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs565487311 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8243756 RMVar_hsa_circ_35397,RMVar_hsa_circ_135404,RMVar_hsa_circ_338255 15878 RMVar_ID_15878 Human_SNP_ID_28178615 A-to-I Human chr1 + 113008738 113008738 113008738 TTGGCTCACAACAACCTCTGCCTCCTGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGC TTGGCTCACAACAACCTCTGCCTCCTGGGTTCGAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGC A G SLC16A1-AS1 Ensembl:ENSG00000226419 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs189776240 Functional Loss SNV dbSNP153 33..33 33 - - - 15879 RMVar_ID_15879 Human_SNP_ID_28178828 A-to-I Human chr1 + 113009487 113009482 113009488 TAAACATGTTTCCATTTTCTCCTTCTGCTTTTATTTTTATTTTTATTTTTTTGAAATGGAGTCTC TAAACATGTTTCCATTTTCTCCTTCTGC______TTTTATTTTTATTTTTTTGAAATGGAGTCTC CTTTTAT C SLC16A1-AS1 Ensembl:ENSG00000226419 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs937587853 Functional Loss DEL dbSNP153 29..34 33 - - - 15880 RMVar_ID_15880 Human_SNP_ID_28178956 A-to-I Human chr1 + 113010035 113010035 113010035 GGGAGGCTGAGGCAGGAGAATCACTTGAACCCAGGAGGTGGAGGTTGCAGTGAGCCGAGATTGTG GGGAGGCTGAGGCAGGAGAATCACTTGAACCCGGGAGGTGGAGGTTGCAGTGAGCCGAGATTGTG A G SLC16A1-AS1 Ensembl:ENSG00000226419 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs868853222 Functional Loss SNV dbSNP153 33..33 33 - - - 15881 RMVar_ID_15881 Human_SNP_ID_28179205 A-to-I Human chr1 + 113010788 113010788 113010788 CTTGGCCACTGCAACCTCCGCCTCCCTGGTTCAAGTGATTCTCCTGCCTCAGGCTCCCGAGTAGC CTTGGCCACTGCAACCTCCGCCTCCCTGGTTCGAGTGATTCTCCTGCCTCAGGCTCCCGAGTAGC A G SLC16A1-AS1 Ensembl:ENSG00000226419 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264092576 Functional Loss SNV dbSNP153 33..33 33 - - - 15882 RMVar_ID_15882 Human_SNP_ID_28179213 A-to-I Human chr1 + 113010836 113010836 113010836 TCAGGCTCCCGAGTAGCTGGGATTCTGGGATTACAGGTGCCTGCCACCATGCCCAGCTAATTTTT TCAGGCTCCCGAGTAGCTGGGATTCTGGGATTGCAGGTGCCTGCCACCATGCCCAGCTAATTTTT A G SLC16A1-AS1 Ensembl:ENSG00000226419 lincRNA intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1221459757 Functional Loss SNV dbSNP153 33..33 33 - - - 15883 RMVar_ID_15883 Human_SNP_ID_28181630 A-to-I Human chr1 + 113021228 113021228 113021228 ATGCCACTGCACTCCAGCCTGGGCGACAGAGCAAGACTCTGTCAAAAAAAAAAAAAAAAAAAATT ATGCCACTGCACTCCAGCCTGGGCGACAGAGCGAGACTCTGTCAAAAAAAAAAAAAAAAAAAATT A G SLC16A1-AS1 Ensembl:ENSG00000226419 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1233841543 Functional Loss SNV dbSNP153 33..33 33 - - - 15884 RMVar_ID_15884 Human_SNP_ID_28183668 A-to-I Human chr1 + 113029236 113029236 113029236 GGCCAGGTGCGGTGGCTCACGCCTGTAATCCCAACACTTTGGGAGGCCGAGGAGGCTGGATCACG GGCCAGGTGCGGTGGCTCACGCCTGTAATCCCTACACTTTGGGAGGCCGAGGAGGCTGGATCACG A T SLC16A1-AS1 Ensembl:ENSG00000226419 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs771766633 Functional Loss SNV dbSNP153 33..33 33 - - - 15885 RMVar_ID_15885 Human_SNP_ID_28196527 A-to-I Human chr1 + 113079221 113079220 113079221 AGTGCAACAGTTAGCCAGGTATGCTGGTACACACCTCTAGTCCCAGTTACTTGGGGGGCTGAGGT AGTGCAACAGTTAGCCAGGTATGCTGGTACAC_CCTCTAGTCCCAGTTACTTGGGGGGCTGAGGT CA C LRIG2 Ensembl:ENSG00000198799 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1316759667 Functional Loss DEL dbSNP153 33..33 33 - - - 15886 RMVar_ID_15886 Human_SNP_ID_28196746 A-to-I Human chr1 + 113079859 113079859 113079859 AGTTCAAGCGATTCTGCTTCAGCCTCCCAAGTAGCTGGGATTACAGGCGCCCACCACCATGCCTA AGTTCAAGCGATTCTGCTTCAGCCTCCCAAGTGGCTGGGATTACAGGCGCCCACCACCATGCCTA A G LRIG2 Ensembl:ENSG00000198799 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs938289465 Functional Loss SNV dbSNP153 33..33 33 - - - 15887 RMVar_ID_15887 Human_SNP_ID_28196751 A-to-I Human chr1 + 113079869 113079869 113079869 ATTCTGCTTCAGCCTCCCAAGTAGCTGGGATTACAGGCGCCCACCACCATGCCTAGCTAATTTTT ATTCTGCTTCAGCCTCCCAAGTAGCTGGGATTGCAGGCGCCCACCACCATGCCTAGCTAATTTTT A G LRIG2 Ensembl:ENSG00000198799 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1053712286 Functional Loss SNV dbSNP153 33..33 33 - - - 15888 RMVar_ID_15888 Human_SNP_ID_28197010 A-to-I Human chr1 + 113080561 113080561 113080561 ACCACCACGCCCGGCTAATTTTTTGTATTTTCAGTAGGACGTGGTTTCACCGTGTTAGCCAGGAT ACCACCACGCCCGGCTAATTTTTTGTATTTTCGGTAGGACGTGGTTTCACCGTGTTAGCCAGGAT A G LRIG2 Ensembl:ENSG00000198799 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs755042270 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5672910,Human_RBP_ID_11179814 15889 RMVar_ID_15889 Human_SNP_ID_28207122 A-to-I Human chr1 + 113119920 113119920 113119920 CAACCTCTGCCTCCCTGGTTCAAGCAATTCTCATGCCTCAGCCTCCCAAGAAGCTGGGACTACAG CAACCTCTGCCTCCCTGGTTCAAGCAATTCTCGTGCCTCAGCCTCCCAAGAAGCTGGGACTACAG A G LRIG2 Ensembl:ENSG00000198799 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs552727095 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_135407 15890 RMVar_ID_15890 Human_SNP_ID_28218186 A-to-I Human chr1 - 113169068 113169068 113169068 TTGGCCACCCATTTGGGGATTTTCAGCTGCCCAGACTTTTTGAGAAAGGCTGCCAGAGCTCTGAC TTGGCCACCCATTTGGGGATTTTCAGCTGCCCGGACTTTTTGAGAAAGGCTGCCAGAGCTCTGAC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1003417169 Functional Loss SNV dbSNP153 33..33 33 - - - 15891 RMVar_ID_15891 Human_SNP_ID_28272652 A-to-I Human chr1 + 113403493 113403493 113403493 TTAATATAATTTAATTGTAATTTTATGCAACTAAATTCTTAATAGTGGCTGTGTTTGACAACTGA TTAATATAATTTAATTGTAATTTTATGCAACTGAATTCTTAATAGTGGCTGTGTTTGACAACTGA A G MAGI3 Ensembl:ENSG00000081026 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1436282245 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124622,RMVar_hsa_circ_135438 15892 RMVar_ID_15892 Human_SNP_ID_28336126 A-to-I Human chr1 - 113685662 113685662 113685662 CACAGTTAACAAAAATAGGATTCGTTATCACTAATTGTGGACTACAGGGAAAATAATAAATAATT CACAGTTAACAAAAATAGGATTCGTTATCACTGATTGTGGACTACAGGGAAAATAATAAATAATT T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs919159143 Functional Loss SNV dbSNP153 33..33 33 - - - 15893 RMVar_ID_15893 Human_SNP_ID_28341053 A-to-I Human chr1 - 113706980 113706980 113706980 ATGGACCTAGCGAGCCATGGTGGTATGTGCCTATGGTCCTTGCTACACAGAAGGCTGTATAGAGG ATGGACCTAGCGAGCCATGGTGGTATGTGCCTGTGGTCCTTGCTACACAGAAGGCTGTATAGAGG T C PHTF1 Ensembl:ENSG00000116793 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935604818 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21702,RMVar_hsa_circ_31599,RMVar_hsa_circ_135467,RMVar_hsa_circ_135470,RMVar_hsa_circ_135468,RMVar_hsa_circ_328214,RMVar_hsa_circ_94506,RMVar_hsa_circ_135477,RMVar_hsa_circ_135474,RMVar_hsa_circ_319005,RMVar_hsa_circ_322253,RMVar_hsa_circ_267195,RMVar_hsa_circ_291024,RMVar_hsa_circ_327483,RMVar_hsa_circ_48796,RMVar_hsa_circ_52505,RMVar_hsa_circ_135479,RMVar_hsa_circ_269581 15894 RMVar_ID_15894 Human_SNP_ID_28342973 A-to-I Human chr1 - 113715615 113715615 113715615 AGACAGGGTTTCACTGTCATTGCTCAGGTTGAAGTGCAATGGTACAATCTCGGCTCACTGCAAAC AGACAGGGTTTCACTGTCATTGCTCAGGTTGAGGTGCAATGGTACAATCTCGGCTCACTGCAAAC T C PHTF1 Ensembl:ENSG00000116793 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991159017 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19171194 RMVar_hsa_circ_21702,RMVar_hsa_circ_31599,RMVar_hsa_circ_328214,RMVar_hsa_circ_94506,RMVar_hsa_circ_135474,RMVar_hsa_circ_319005,RMVar_hsa_circ_29441,RMVar_hsa_circ_52505,RMVar_hsa_circ_57013,RMVar_hsa_circ_339192,RMVar_hsa_circ_359274,RMVar_hsa_circ_135480,RMVar_hsa_circ_135481,RMVar_hsa_circ_329485,RMVar_hsa_circ_348289 15895 RMVar_ID_15895 Human_SNP_ID_28347072 A-to-I Human chr1 - 113733054 113733054 113733054 CAAAAAAAAAAAAAAAAAAAAAAAAATTAGCCAGGCGTGGTGCAAGCCTGTAGTTTCAACTACCT CAAAAAAAAAAAAAAAAAAAAAAAAATTAGCCGGGCGTGGTGCAAGCCTGTAGTTTCAACTACCT T C PHTF1 Ensembl:ENSG00000116793 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1448712276 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21702,RMVar_hsa_circ_31599,RMVar_hsa_circ_328214,RMVar_hsa_circ_135485,RMVar_hsa_circ_57013,RMVar_hsa_circ_359274,RMVar_hsa_circ_321406,RMVar_hsa_circ_273778,RMVar_hsa_circ_135486,RMVar_hsa_circ_348492,RMVar_hsa_circ_318366 15896 RMVar_ID_15896 Human_SNP_ID_28350485 A-to-I Human chr1 - 113748116 113748116 113748116 AAAATCAGCTGGGTGTAGTGGTGTGTGCCTGTAGTCGCAGCTACTCAGACGGCTGAGGTGAAAGG AAAATCAGCTGGGTGTAGTGGTGTGTGCCTGTCGTCGCAGCTACTCAGACGGCTGAGGTGAAAGG T G PHTF1 Ensembl:ENSG00000116793 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1399454982 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21702,RMVar_hsa_circ_328214,RMVar_hsa_circ_57013,RMVar_hsa_circ_321406,RMVar_hsa_circ_318366,RMVar_hsa_circ_308486,RMVar_hsa_circ_365452 15897 RMVar_ID_15897 Human_SNP_ID_28350579 A-to-I Human chr1 - 113748709 113748709 113748709 CAACATGGTGATACCCTGTCTTTACAAAAAATACAAAAAAATTAGCTGGGCTTGGCGTTGCATGC CAACATGGTGATACCCTGTCTTTACAAAAAATGCAAAAAAATTAGCTGGGCTTGGCGTTGCATGC T C PHTF1 Ensembl:ENSG00000116793 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs570586666 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21702,RMVar_hsa_circ_328214,RMVar_hsa_circ_57013,RMVar_hsa_circ_321406,RMVar_hsa_circ_318366,RMVar_hsa_circ_308486,RMVar_hsa_circ_365452 15898 RMVar_ID_15898 Human_SNP_ID_28373897 A-to-I Human chr1 - 113850158 113850158 113850158 GAGTTTCACACTGTCACTCAGGCTGGAGTGCAATGGTGCGATCTTGGCTCACTGCAACTTCTGCC GAGTTTCACACTGTCACTCAGGCTGGAGTGCAGTGGTGCGATCTTGGCTCACTGCAACTTCTGCC T C PTPN22 Ensembl:ENSG00000134242 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs187671888 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_366168,RMVar_hsa_circ_53861,RMVar_hsa_circ_350452,RMVar_hsa_circ_360366,RMVar_hsa_circ_69683,RMVar_hsa_circ_135497,RMVar_hsa_circ_311660,RMVar_hsa_circ_376995,RMVar_hsa_circ_135498,RMVar_hsa_circ_353048,RMVar_hsa_circ_359941,RMVar_hsa_circ_47487,RMVar_hsa_circ_355394,RMVar_hsa_circ_59961,RMVar_hsa_circ_289763,RMVar_hsa_circ_135499 15899 RMVar_ID_15899 Human_SNP_ID_28374181 A-to-I Human chr1 - 113851327 113851327 113851327 CAATATGCTGAAACCCTGTCTCTACTAAAAATAAAAAAATTAGCTGGATATGGTGGCAGGCACCT CAATATGCTGAAACCCTGTCTCTACTAAAAATTAAAAAATTAGCTGGATATGGTGGCAGGCACCT T A PTPN22 Ensembl:ENSG00000134242 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1248920689 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_366168,RMVar_hsa_circ_53861,RMVar_hsa_circ_350452,RMVar_hsa_circ_360366,RMVar_hsa_circ_69683,RMVar_hsa_circ_135497,RMVar_hsa_circ_311660,RMVar_hsa_circ_376995,RMVar_hsa_circ_135498,RMVar_hsa_circ_353048,RMVar_hsa_circ_359941,RMVar_hsa_circ_47487,RMVar_hsa_circ_355394,RMVar_hsa_circ_59961,RMVar_hsa_circ_289763,RMVar_hsa_circ_135499 15900 RMVar_ID_15900 Human_SNP_ID_28375118 A-to-I Human chr1 - 113855448 113855448 113855448 CCAGTCTGGAGTGTGGAGTGTGCAGTGGTGCAATCTTGGCTTACTGCAACCTGAGCCTCCTGGGT CCAGTCTGGAGTGTGGAGTGTGCAGTGGTGCAGTCTTGGCTTACTGCAACCTGAGCCTCCTGGGT T C PTPN22 Ensembl:ENSG00000134242 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1044494140 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59961 15901 RMVar_ID_15901 Human_SNP_ID_28375304 A-to-I Human chr1 - 113856097 113856097 113856097 GGCAGGAGAAATCATTTAAGCCCTGGAGGTGGAGGTTGCAGTGAACCGAGATGGTGCCACTGTAC GGCAGGAGAAATCATTTAAGCCCTGGAGGTGGTGGTTGCAGTGAACCGAGATGGTGCCACTGTAC T A PTPN22 Ensembl:ENSG00000134242 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1488047019 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59961 15902 RMVar_ID_15902 Human_SNP_ID_28380353 A-to-I Human chr1 - 113878978 113878978 113878978 AGGCTTGGTGGCACGTGCCTGTAATGCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAA AGGCTTGGTGGCACGTGCCTGTAATGCCAGCTGCTCAGGAGGCTGAGGCAGGAGAATCACTTGAA T C BCL2L15 Ensembl:ENSG00000188761 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs539810148 Functional Loss SNV dbSNP153 33..33 33 - - - 15903 RMVar_ID_15903 Human_SNP_ID_28380361 A-to-I Human chr1 - 113879010 113879010 113879010 CCTGTCTCTGCTAAAAATACAAAAAATTAGCCAGGCTTGGTGGCACGTGCCTGTAATGCCAGCTA CCTGTCTCTGCTAAAAATACAAAAAATTAGCCGGGCTTGGTGGCACGTGCCTGTAATGCCAGCTA T C BCL2L15 Ensembl:ENSG00000188761 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1163687815 Functional Loss SNV dbSNP153 33..33 33 - - - 15904 RMVar_ID_15904 Human_SNP_ID_28380790 A-to-I Human chr1 - 113880504 113880504 113880504 CTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGAGCCCGCCATCACGCCCGGCTAATTTTT CTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTGCAGGAGCCCGCCATCACGCCCGGCTAATTTTT T C BCL2L15 Ensembl:ENSG00000188761 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs557896231 Functional Loss SNV dbSNP153 33..33 33 - - - 15905 RMVar_ID_15905 Human_SNP_ID_28391379 A-to-I Human chr1 - 113920628 113920628 113920628 CCCAGGCGAGAGGATCATGAGGCCAGGAGTTCAAGACCAGCCTGGGCAACATAGTGAGACCACAT CCCAGGCGAGAGGATCATGAGGCCAGGAGTTCGAGACCAGCCTGGGCAACATAGTGAGACCACAT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910781094 Functional Loss SNV dbSNP153 33..33 33 - - - 15906 RMVar_ID_15906 Human_SNP_ID_28404863 A-to-I Human chr1 + 113974946 113974946 113974946 ATTGATGTCTCCATTGTATTTAAACCAAAATGAACTGATACTTGTTGGAATGTATGTGAACTAAT ATTGATGTCTCCATTGTATTTAAACCAAAATGGACTGATACTTGTTGGAATGTATGTGAACTAAT A G HIPK1 Ensembl:ENSG00000163349 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs528783706 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_321954,Human_RBP_ID_1408784,Human_RBP_ID_1722801,Human_RBP_ID_2087190,Human_RBP_ID_8281712,Human_RBP_ID_8945076,Human_RBP_ID_10532705,Human_RBP_ID_18215109,Human_RBP_ID_21879150,Human_RBP_ID_23324628,Human_RBP_ID_26389578,Human_RBP_ID_27576851 Human_miRNA_ID_1782418 15907 RMVar_ID_15907 Human_SNP_ID_28514797 A-to-I Human chr1 - 114413807 114413807 114413807 CTAATAGTTGACTAGACTGGTTTTGAACTCCTAGTCTCAAGTGATCCTCTTACCTTGGTATCCGA CTAATAGTTGACTAGACTGGTTTTGAACTCCTGGTCTCAAGTGATCCTCTTACCTTGGTATCCGA T C TRIM33 Ensembl:ENSG00000197323 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs543909580 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10533853 RMVar_hsa_circ_74288,RMVar_hsa_circ_135531,RMVar_hsa_circ_112335,RMVar_hsa_circ_135533,RMVar_hsa_circ_135535,RMVar_hsa_circ_75355,RMVar_hsa_circ_116113 15908 RMVar_ID_15908 Human_SNP_ID_28515242 A-to-I Human chr1 - 114415242 114415242 114415242 CTGTAGTCCCAGCACTTTGAGGAGGCCAAGATAGGAAGAGCACTTGAGGCCAGGAGTTCGAGACT CTGTAGTCCCAGCACTTTGAGGAGGCCAAGATGGGAAGAGCACTTGAGGCCAGGAGTTCGAGACT T C TRIM33 Ensembl:ENSG00000197323 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs552142424 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10533918,Human_RBP_ID_24750636 RMVar_hsa_circ_74288,RMVar_hsa_circ_135531,RMVar_hsa_circ_112335,RMVar_hsa_circ_135533,RMVar_hsa_circ_135535,RMVar_hsa_circ_75355,RMVar_hsa_circ_116113 15909 RMVar_ID_15909 Human_SNP_ID_28515244 A-to-I Human chr1 - 114415261 114415261 114415261 CTGGGTGCAGTGGCTCTGCCTGTAGTCCCAGCACTTTGAGGAGGCCAAGATAGGAAGAGCACTTG CTGGGTGCAGTGGCTCTGCCTGTAGTCCCAGCGCTTTGAGGAGGCCAAGATAGGAAGAGCACTTG T C TRIM33 Ensembl:ENSG00000197323 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs965215863 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10533919 RMVar_hsa_circ_74288,RMVar_hsa_circ_135531,RMVar_hsa_circ_112335,RMVar_hsa_circ_135533,RMVar_hsa_circ_135535,RMVar_hsa_circ_75355,RMVar_hsa_circ_116113 15910 RMVar_ID_15910 Human_SNP_ID_28534079 A-to-I Human chr1 - 114490498 114490498 114490498 GAGTGCAATTGCTGGGTTGTGTGGTAACTTATATTTAATCTTTTGAGGATCTGCCAACTGTTATC GAGTGCAATTGCTGGGTTGTGTGGTAACTTATGTTTAATCTTTTGAGGATCTGCCAACTGTTATC T C TRIM33 Ensembl:ENSG00000197323 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1443927892 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10535516 15911 RMVar_ID_15911 Human_SNP_ID_28537057 A-to-I Human chr1 - 114502782 114502782 114502782 ACCTGTCGTGCCGGACATGGTGGCTCATGCCTATAATCCCAGCACTTTCGAAGGCTGAGGTGGGA ACCTGTCGTGCCGGACATGGTGGCTCATGCCTGTAATCCCAGCACTTTCGAAGGCTGAGGTGGGA T C TRIM33 Ensembl:ENSG00000197323 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1557906304 Functional Loss SNV dbSNP153 33..33 33 - - - 15912 RMVar_ID_15912 Human_SNP_ID_28545128 A-to-I Human chr1 - 114536211 114536211 114536211 GTACTCATGAGTTCCATGAGAGAAGTTCAGACAAGCCACATTCGTTCCAGACTTAATCATCTCCT GTACTCATGAGTTCCATGAGAGAAGTTCAGACGAGCCACATTCGTTCCAGACTTAATCATCTCCT T C lnc-BCAS2-3 RNACentral:URS00008C2D41 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs976746319 Functional Loss SNV dbSNP153 33..33 33 - - - 15913 RMVar_ID_15913 Human_SNP_ID_28545275 A-to-I Human chr1 + 114536824 114536824 114536824 AATCAACACAATCGAGAATCATGTGGGGGTTCAGAGGTTTGATGAAATCCTAGAGGCCAGTGATG AATCAACACAATCGAGAATCATGTGGGGGTTCGGAGGTTTGATGAAATCCTAGAGGCCAGTGATG A G PKMP1 Ensembl:ENSG00000236480 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879130265 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5891083 Human_miRNA_ID_1854138,Human_miRNA_ID_1910207 15914 RMVar_ID_15914 Human_SNP_ID_28556131 A-to-I Human chr1 - 114580009 114580009 114580009 GGATCACTTGAGCCTGGGAGTTCAAGACTGCTACAGTGAGCCATGATAATGCCATTGCACTCCAG GGATCACTTGAGCCTGGGAGTTCAAGACTGCTGCAGTGAGCCATGATAATGCCATTGCACTCCAG T C BCAS2 Ensembl:ENSG00000116752 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1050100536 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111957,RMVar_hsa_circ_135549,RMVar_hsa_circ_135551,RMVar_hsa_circ_83773 15915 RMVar_ID_15915 Human_SNP_ID_28556159 A-to-I Human chr1 - 114580137 114580137 114580137 TGAGGATCACTTGAGACCAGCCTGGGCAACATAGTGAGACCCTTTCTCTACAAAAGAAAAATTAA TGAGGATCACTTGAGACCAGCCTGGGCAACATGGTGAGACCCTTTCTCTACAAAAGAAAAATTAA T C BCAS2 Ensembl:ENSG00000116752 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs59219923 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_1141 RMVar_hsa_circ_111957,RMVar_hsa_circ_135549,RMVar_hsa_circ_135551,RMVar_hsa_circ_83773 15916 RMVar_ID_15916 Human_SNP_ID_28557246 A-to-I Human chr1 - 114583685 114583685 114583685 CTCCTGCCTCAGCCTCCTGAGTAGCTGGAATTATAGGCACCCGCCACCACACCTGGCTAATTTTG CTCCTGCCTCAGCCTCCTGAGTAGCTGGAATTCTAGGCACCCGCCACCACACCTGGCTAATTTTG T G DENND2C Ensembl:ENSG00000175984 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1557934800 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111957,RMVar_hsa_circ_135549,RMVar_hsa_circ_135551,RMVar_hsa_circ_83773 15917 RMVar_ID_15917 Human_SNP_ID_28557431 A-to-I Human chr1 - 114584364 114584364 114584364 GGGAGGCTGAGCCATGAGAATCGCTTGAGCCCAGGAGGCAGAGGTTGCAGTGAGCCGAGATCGCG GGGAGGCTGAGCCATGAGAATCGCTTGAGCCCGGGAGGCAGAGGTTGCAGTGAGCCGAGATCGCG T C DENND2C Ensembl:ENSG00000175984 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042882377 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111957,RMVar_hsa_circ_135549,RMVar_hsa_circ_135551,RMVar_hsa_circ_83773 15918 RMVar_ID_15918 Human_SNP_ID_28557467 A-to-I Human chr1 - 114584526 114584526 114584526 CACGTCTGTAATCCCAGCACTATGGGAGTCCAAGGCGAGTGGATCATTTGAGGTCAGGAGTTCGA CACGTCTGTAATCCCAGCACTATGGGAGTCCAGGGCGAGTGGATCATTTGAGGTCAGGAGTTCGA T C DENND2C Ensembl:ENSG00000175984 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs776435322 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111957,RMVar_hsa_circ_135549,RMVar_hsa_circ_135551,RMVar_hsa_circ_83773 15919 RMVar_ID_15919 Human_SNP_ID_28586456 A-to-I Human chr1 - 114705880 114705879 114705880 CTTGTGCCAATAGCCCTTGTATGTATGTACTTAGAGTTTTCCAAGTATGTTCTAAGCACAGAAGT CTTGTGCCAATAGCCCTTGTATGTATGTACTT_GAGTTTTCCAAGTATGTTCTAAGCACAGAAGT CT C NRAS Ensembl:ENSG00000213281 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs770180355 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_322244,Human_RBP_ID_1722953,Human_RBP_ID_5675686,Human_RBP_ID_8733051,Human_RBP_ID_18215253,Human_RBP_ID_18548290,Human_RBP_ID_23325134,Human_RBP_ID_26386276,Human_RBP_ID_27577021 RMVar_hsa_circ_93833,RMVar_hsa_circ_135553 15920 RMVar_ID_15920 Human_SNP_ID_28586457 A-to-I Human chr1 - 114705880 114705880 114705880 CTTGTGCCAATAGCCCTTGTATGTATGTACTTAGAGTTTTCCAAGTATGTTCTAAGCACAGAAGT CTTGTGCCAATAGCCCTTGTATGTATGTACTTCGAGTTTTCCAAGTATGTTCTAAGCACAGAAGT T G NRAS Ensembl:ENSG00000213281 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs929744422 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_322244,Human_RBP_ID_1722953,Human_RBP_ID_5675686,Human_RBP_ID_8733051,Human_RBP_ID_18215253,Human_RBP_ID_18548290,Human_RBP_ID_23325134,Human_RBP_ID_26386276,Human_RBP_ID_27577021 RMVar_hsa_circ_93833,RMVar_hsa_circ_135553 15921 RMVar_ID_15921 Human_SNP_ID_28602179 A-to-I Human chr1 - 114770249 114770249 114770249 GGGATTACAAGTGCCCACCACCATGCACAGCTAATTTTTGTGTTTTTAGTAGATGGGGTTTCTCC GGGATTACAAGTGCCCACCACCATGCACAGCTGATTTTTGTGTTTTTAGTAGATGGGGTTTCTCC T C SIKE1 Ensembl:ENSG00000052723 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1327792426 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10539051 15922 RMVar_ID_15922 Human_SNP_ID_28602202 A-to-I Human chr1 - 114770314 114770314 114770314 TAACTCACTGCAACCTCCACCTCCTGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTCGCT TAACTCACTGCAACCTCCACCTCCTGGGTTCACGCGATTCTCCTGCCTCAGCCTCCCAAGTCGCT T G SIKE1 Ensembl:ENSG00000052723 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1050178141 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_322523 15923 RMVar_ID_15923 Human_SNP_ID_29034398 A-to-I Human chr1 - 116543860 116543860 116543860 AGAGTGCAGTGGCACAATCTTGGCTGACTGCAACCTCTGCCTCCCAGGTTCAAAGTGATTTTACT AGAGTGCAGTGGCACAATCTTGGCTGACTGCAGCCTCTGCCTCCCAGGTTCAAAGTGATTTTACT T C CD58 Ensembl:ENSG00000116815 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1294811143 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_135630,RMVar_hsa_circ_127652,RMVar_hsa_circ_308373,RMVar_hsa_circ_135629,RMVar_hsa_circ_337504 15924 RMVar_ID_15924 Human_SNP_ID_29036530 A-to-I Human chr1 - 116553626 116553626 116553626 AGACCCCTCACACTGAACAGTGTCAAACTGAAAGCATGATGTTCCAGGCCAGTCTTAGTCTTCCT AGACCCCTCACACTGAACAGTGTCAAACTGAAGGCATGATGTTCCAGGCCAGTCTTAGTCTTCCT T C CD58 Ensembl:ENSG00000116815 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569748709 Functional Loss SNV dbSNP153 33..33 33 - - - 15925 RMVar_ID_15925 Human_SNP_ID_29164541 A-to-I Human chr1 + 117082237 117082235 117082238 TAAGCATAATAATAATTCTTATTTTTTGAGACAGGGTCTCGCTCTGTTGCTCAGGCTGGAGTGCA TAAGCATAATAATAATTCTTATTTTTTGAGA___GGTCTCGCTCTGTTGCTCAGGCTGGAGTGCA ACAG A TTF2 Ensembl:ENSG00000116830 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1553196701 Functional Loss DEL dbSNP153 32..34 33 - - - Human_miRNA_ID_1949954,Human_miRNA_ID_1951238,Human_miRNA_ID_2443323 RMVar_hsa_circ_116031,RMVar_hsa_circ_119088,RMVar_hsa_circ_96197,RMVar_hsa_circ_135648,RMVar_hsa_circ_135649,RMVar_hsa_circ_135651,RMVar_hsa_circ_92212,RMVar_hsa_circ_135654,RMVar_hsa_circ_101578,RMVar_hsa_circ_110065,RMVar_hsa_circ_135652,RMVar_hsa_circ_80085,RMVar_hsa_circ_135655,RMVar_hsa_circ_126216,RMVar_hsa_circ_135653,RMVar_hsa_circ_120763,RMVar_hsa_circ_135656,RMVar_hsa_circ_110780,RMVar_hsa_circ_93760,RMVar_hsa_circ_135658,RMVar_hsa_circ_98395,RMVar_hsa_circ_135659,RMVar_hsa_circ_135660,RMVar_hsa_circ_78374,RMVar_hsa_circ_88077,RMVar_hsa_circ_135661,RMVar_hsa_circ_135662,RMVar_hsa_circ_135663 15926 RMVar_ID_15926 Human_SNP_ID_29164542 A-to-I Human chr1 + 117082237 117082236 117082238 TAAGCATAATAATAATTCTTATTTTTTGAGACAGGGTCTCGCTCTGTTGCTCAGGCTGGAGTGCA TAAGCATAATAATAATTCTTATTTTTTGAGAC__GGTCTCGCTCTGTTGCTCAGGCTGGAGTGCA CAG C TTF2 Ensembl:ENSG00000116830 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs5777297 Functional Loss DEL dbSNP153 33..34 33 - - - Human_miRNA_ID_1949954,Human_miRNA_ID_1951238,Human_miRNA_ID_2443323 RMVar_hsa_circ_116031,RMVar_hsa_circ_119088,RMVar_hsa_circ_96197,RMVar_hsa_circ_135648,RMVar_hsa_circ_135649,RMVar_hsa_circ_135651,RMVar_hsa_circ_92212,RMVar_hsa_circ_135654,RMVar_hsa_circ_101578,RMVar_hsa_circ_110065,RMVar_hsa_circ_135652,RMVar_hsa_circ_80085,RMVar_hsa_circ_135655,RMVar_hsa_circ_126216,RMVar_hsa_circ_135653,RMVar_hsa_circ_120763,RMVar_hsa_circ_135656,RMVar_hsa_circ_110780,RMVar_hsa_circ_93760,RMVar_hsa_circ_135658,RMVar_hsa_circ_98395,RMVar_hsa_circ_135659,RMVar_hsa_circ_135660,RMVar_hsa_circ_78374,RMVar_hsa_circ_88077,RMVar_hsa_circ_135661,RMVar_hsa_circ_135662,RMVar_hsa_circ_135663 15927 RMVar_ID_15927 Human_SNP_ID_29164546 A-to-I Human chr1 + 117082237 117082237 117082237 TAAGCATAATAATAATTCTTATTTTTTGAGACAGGGTCTCGCTCTGTTGCTCAGGCTGGAGTGCA TAAGCATAATAATAATTCTTATTTTTTGAGACGGGGTCTCGCTCTGTTGCTCAGGCTGGAGTGCA A G TTF2 Ensembl:ENSG00000116830 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs200199061 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1949954,Human_miRNA_ID_1951238,Human_miRNA_ID_2443323 RMVar_hsa_circ_116031,RMVar_hsa_circ_119088,RMVar_hsa_circ_96197,RMVar_hsa_circ_135648,RMVar_hsa_circ_135649,RMVar_hsa_circ_135651,RMVar_hsa_circ_92212,RMVar_hsa_circ_135654,RMVar_hsa_circ_101578,RMVar_hsa_circ_110065,RMVar_hsa_circ_135652,RMVar_hsa_circ_80085,RMVar_hsa_circ_135655,RMVar_hsa_circ_126216,RMVar_hsa_circ_135653,RMVar_hsa_circ_120763,RMVar_hsa_circ_135656,RMVar_hsa_circ_110780,RMVar_hsa_circ_93760,RMVar_hsa_circ_135658,RMVar_hsa_circ_98395,RMVar_hsa_circ_135659,RMVar_hsa_circ_135660,RMVar_hsa_circ_78374,RMVar_hsa_circ_88077,RMVar_hsa_circ_135661,RMVar_hsa_circ_135662,RMVar_hsa_circ_135663 15928 RMVar_ID_15928 Human_SNP_ID_29164572 A-to-I Human chr1 + 117082325 117082325 117082325 GCCTAAACCTCCTTGGCTCAAGCGATCCTCCCACCTCAGCCTCCCAAGTAGCTGGGACCACAAGT GCCTAAACCTCCTTGGCTCAAGCGATCCTCCCGCCTCAGCCTCCCAAGTAGCTGGGACCACAAGT A G TTF2 Ensembl:ENSG00000116830 Protein coding intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1466990640 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2712217,Human_miRNA_ID_3048201 RMVar_hsa_circ_116031,RMVar_hsa_circ_119088,RMVar_hsa_circ_96197,RMVar_hsa_circ_135648,RMVar_hsa_circ_135649,RMVar_hsa_circ_135651,RMVar_hsa_circ_92212,RMVar_hsa_circ_135654,RMVar_hsa_circ_101578,RMVar_hsa_circ_110065,RMVar_hsa_circ_135652,RMVar_hsa_circ_80085,RMVar_hsa_circ_135655,RMVar_hsa_circ_126216,RMVar_hsa_circ_135653,RMVar_hsa_circ_120763,RMVar_hsa_circ_135656,RMVar_hsa_circ_110780,RMVar_hsa_circ_93760,RMVar_hsa_circ_135658,RMVar_hsa_circ_98395,RMVar_hsa_circ_135659,RMVar_hsa_circ_135660,RMVar_hsa_circ_78374,RMVar_hsa_circ_88077,RMVar_hsa_circ_135661,RMVar_hsa_circ_135662,RMVar_hsa_circ_135663 15929 RMVar_ID_15929 Human_SNP_ID_29164574 A-to-I Human chr1 + 117082338 117082338 117082338 TGGCTCAAGCGATCCTCCCACCTCAGCCTCCCAAGTAGCTGGGACCACAAGTTTGCACCACCACA TGGCTCAAGCGATCCTCCCACCTCAGCCTCCCGAGTAGCTGGGACCACAAGTTTGCACCACCACA A G TTF2 Ensembl:ENSG00000116830 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1172325813 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116031,RMVar_hsa_circ_119088,RMVar_hsa_circ_96197,RMVar_hsa_circ_135648,RMVar_hsa_circ_135649,RMVar_hsa_circ_135651,RMVar_hsa_circ_92212,RMVar_hsa_circ_135654,RMVar_hsa_circ_101578,RMVar_hsa_circ_110065,RMVar_hsa_circ_135652,RMVar_hsa_circ_80085,RMVar_hsa_circ_135655,RMVar_hsa_circ_126216,RMVar_hsa_circ_135653,RMVar_hsa_circ_120763,RMVar_hsa_circ_135656,RMVar_hsa_circ_110780,RMVar_hsa_circ_93760,RMVar_hsa_circ_135658,RMVar_hsa_circ_98395,RMVar_hsa_circ_135659,RMVar_hsa_circ_135660,RMVar_hsa_circ_78374,RMVar_hsa_circ_88077,RMVar_hsa_circ_135661,RMVar_hsa_circ_135662,RMVar_hsa_circ_135663 15930 RMVar_ID_15930 Human_SNP_ID_29165093 A-to-I Human chr1 + 117084430 117084430 117084430 AGGCCTGAGATGCCGGAGCTGCCATTCAGGTGACAGCAGCATTCCCCTAGTCAAGGAGATGTGTC AGGCCTGAGATGCCGGAGCTGCCATTCAGGTGGCAGCAGCATTCCCCTAGTCAAGGAGATGTGTC A G TTF2 Ensembl:ENSG00000116830 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2801937 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116031,RMVar_hsa_circ_135649,RMVar_hsa_circ_135654,RMVar_hsa_circ_110065,RMVar_hsa_circ_80085,RMVar_hsa_circ_135655,RMVar_hsa_circ_51369,RMVar_hsa_circ_93760,RMVar_hsa_circ_135660,RMVar_hsa_circ_78374,RMVar_hsa_circ_86925,RMVar_hsa_circ_135663,RMVar_hsa_circ_306310,RMVar_hsa_circ_76433,RMVar_hsa_circ_135664,RMVar_hsa_circ_135665,RMVar_hsa_circ_135666 15931 RMVar_ID_15931 Human_SNP_ID_29166020 A-to-I Human chr1 + 117088433 117088433 117088433 GTGGCGGGCGCCTGTGGTCCCGGCTGCTCGGGAGGCTGAGGCAGGAGAATGGCGTGAAGCCCGGA GTGGCGGGCGCCTGTGGTCCCGGCTGCTCGGGCGGCTGAGGCAGGAGAATGGCGTGAAGCCCGGA A C TTF2 Ensembl:ENSG00000116830 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1002182143 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_96288,Human_RBP_ID_10541560,Human_RBP_ID_23326146 RMVar_hsa_circ_110065,RMVar_hsa_circ_135655,RMVar_hsa_circ_51369,RMVar_hsa_circ_93760,RMVar_hsa_circ_135660,RMVar_hsa_circ_78374,RMVar_hsa_circ_86925,RMVar_hsa_circ_135663,RMVar_hsa_circ_76433,RMVar_hsa_circ_135664,RMVar_hsa_circ_135665,RMVar_hsa_circ_107468,RMVar_hsa_circ_352072,RMVar_hsa_circ_135667 15932 RMVar_ID_15932 Human_SNP_ID_29169272 A-to-I Human chr1 + 117102013 117102013 117102013 AGAATAAAAAAATGAGCTAGGCGTGGTAGTGCACACCTGTAGTCCTAGCTACTTGGGAGGCTGAG AGAATAAAAAAATGAGCTAGGCGTGGTAGTGCCCACCTGTAGTCCTAGCTACTTGGGAGGCTGAG A C TTF2 Ensembl:ENSG00000116830 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1353907512 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8282404 RMVar_hsa_circ_76433,RMVar_hsa_circ_135664 15933 RMVar_ID_15933 Human_SNP_ID_29241278 A-to-I Human chr1 + 117397721 117397721 117397721 TGGCCCAGGCTGGAGTGCAATGTCACGATCTCAGCTTAGTGAAACCTCCGCCTCCCAGGTTCAAG TGGCCCAGGCTGGAGTGCAATGTCACGATCTCGGCTTAGTGAAACCTCCGCCTCCCAGGTTCAAG A G MAN1A2 Ensembl:ENSG00000198162 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1019273174 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94822,RMVar_hsa_circ_126555,RMVar_hsa_circ_135674,RMVar_hsa_circ_135671,RMVar_hsa_circ_135672,RMVar_hsa_circ_135673 15934 RMVar_ID_15934 Human_SNP_ID_29297207 A-to-I Human chr1 + 117638828 117638828 117638828 GGGCCACTGAAAGCTTTTAGTGGGGGAGTGACAAGAGAAACACCTGCATACAGCAGCTGCTTGGG GGGCCACTGAAAGCTTTTAGTGGGGGAGTGACGAGAGAAACACCTGCATACAGCAGCTGCTTGGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs542248282 Functional Loss SNV dbSNP153 33..33 33 - - - 15935 RMVar_ID_15935 Human_SNP_ID_29366414 A-to-I Human chr1 + 117931052 117931052 117931052 TCACTGCAACCTCGAACTTCTGGACTCAAGTGATCTTTCTGCCTCAGCCTCCCCGAGTGCGTCAC TCACTGCAACCTCGAACTTCTGGACTCAAGTGGTCTTTCTGCCTCAGCCTCCCCGAGTGCGTCAC A G WDR3 Ensembl:ENSG00000065183 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1284615817 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10543984 15936 RMVar_ID_15936 Human_SNP_ID_29374393 A-to-I Human chr1 + 117963509 117963509 117963509 CCTCAGCCTCCAGAGTAGCTGGGACTACAGGCACCCGCCACCACACTTGGCTGATTTTTTCTATT CCTCAGCCTCCAGAGTAGCTGGGACTACAGGCCCCCGCCACCACACTTGGCTGATTTTTTCTATT A C WDR3 Ensembl:ENSG00000065183 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053789421 Functional Loss SNV dbSNP153 33..33 33 - - - 15937 RMVar_ID_15937 Human_SNP_ID_29374394 A-to-I Human chr1 + 117963509 117963509 117963509 CCTCAGCCTCCAGAGTAGCTGGGACTACAGGCACCCGCCACCACACTTGGCTGATTTTTTCTATT CCTCAGCCTCCAGAGTAGCTGGGACTACAGGCGCCCGCCACCACACTTGGCTGATTTTTTCTATT A G WDR3 Ensembl:ENSG00000065183 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053789421 Functional Loss SNV dbSNP153 33..33 33 - - - 15938 RMVar_ID_15938 Human_SNP_ID_29374395 A-to-I Human chr1 + 117963509 117963509 117963509 CCTCAGCCTCCAGAGTAGCTGGGACTACAGGCACCCGCCACCACACTTGGCTGATTTTTTCTATT CCTCAGCCTCCAGAGTAGCTGGGACTACAGGCTCCCGCCACCACACTTGGCTGATTTTTTCTATT A T WDR3 Ensembl:ENSG00000065183 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053789421 Functional Loss SNV dbSNP153 33..33 33 - - - 15939 RMVar_ID_15939 Human_SNP_ID_29564335 A-to-I Human chr1 + 118713578 118713566 118713579 GAGGCTTTGTGGTATGGGACACACCGTGGACCACCAGCAGCAGTAAGAAGGCTCCTGACATGAGC GAGGCTTTGTGGTATGGGACA_____________CAGCAGCAGTAAGAAGGCTCCTGACATGAGC ACACCGTGGACCAC A AL139148.1 Ensembl:ENSG00000229911 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1301197144 Functional Loss DEL dbSNP153 22..34 33 - - - 15940 RMVar_ID_15940 Human_SNP_ID_29648898 A-to-I Human chr1 - 119051822 119051822 119051822 CTGGGAAGGTGGAGGTTGCCGATCGCGCCACTACACTCCAGCCTGGGCAACAGAGTGAGACCTTG CTGGGAAGGTGGAGGTTGCCGATCGCGCCACTGCACTCCAGCCTGGGCAACAGAGTGAGACCTTG T C WARS2 Ensembl:ENSG00000116874 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1198120548 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_135726,RMVar_hsa_circ_339061,RMVar_hsa_circ_371515,RMVar_hsa_circ_135725,RMVar_hsa_circ_135727,RMVar_hsa_circ_12153,RMVar_hsa_circ_122520,RMVar_hsa_circ_135728 15941 RMVar_ID_15941 Human_SNP_ID_29653378 A-to-I Human chr1 - 119071071 119071071 119071071 TCAAACAATTCTCCTGCCTCAGCCTCCCAAGTAGTTGGGATTACAGGCGCCTGCCACCAAGCTTG TCAAACAATTCTCCTGCCTCAGCCTCCCAAGTGGTTGGGATTACAGGCGCCTGCCACCAAGCTTG T C WARS2 Ensembl:ENSG00000116874 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1179671973 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_135726,RMVar_hsa_circ_339061,RMVar_hsa_circ_371515,RMVar_hsa_circ_135725,RMVar_hsa_circ_135727,RMVar_hsa_circ_12153,RMVar_hsa_circ_122520,RMVar_hsa_circ_135728 15942 RMVar_ID_15942 Human_SNP_ID_29668926 A-to-I Human chr1 + 119141312 119141312 119141312 CCTCGGCCTCCTAAAGTGCTGGGATTACAGGCATGTGCCACCGCACTGGACTTATGTGGCCTTAT CCTCGGCCTCCTAAAGTGCTGGGATTACAGGCTTGTGCCACCGCACTGGACTTATGTGGCCTTAT A T WARS2-AS1 Ensembl:ENSG00000231365 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1343200130 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5244974 15943 RMVar_ID_15943 Human_SNP_ID_29673322 A-to-I Human chr1 + 119157447 119157447 119157447 ACCCCACACCCGGCTAATTTTTTTGTATTTTTAGTTGAGACGAGGTTTTGCCATGTGCTGGCTAG ACCCCACACCCGGCTAATTTTTTTGTATTTTTCGTTGAGACGAGGTTTTGCCATGTGCTGGCTAG A C WARS2-AS1 Ensembl:ENSG00000231365 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs921026012 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10546474,Human_RBP_ID_17096923,Human_RBP_ID_19177045 RMVar_hsa_circ_86930,RMVar_hsa_circ_135731 15944 RMVar_ID_15944 Human_SNP_ID_29673323 A-to-I Human chr1 + 119157447 119157447 119157447 ACCCCACACCCGGCTAATTTTTTTGTATTTTTAGTTGAGACGAGGTTTTGCCATGTGCTGGCTAG ACCCCACACCCGGCTAATTTTTTTGTATTTTTGGTTGAGACGAGGTTTTGCCATGTGCTGGCTAG A G WARS2-AS1 Ensembl:ENSG00000231365 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs921026012 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10546474,Human_RBP_ID_17096923,Human_RBP_ID_19177045 RMVar_hsa_circ_86930,RMVar_hsa_circ_135731 15945 RMVar_ID_15945 Human_SNP_ID_29673562 A-to-I Human chr1 + 119158399 119158399 119158399 ATCATGATCTCTTGGCATCAAGCAGTCCTCCCACCTCAGCCTCCAAAGTGCTGGGATTACAGGTC ATCATGATCTCTTGGCATCAAGCAGTCCTCCCGCCTCAGCCTCCAAAGTGCTGGGATTACAGGTC A G WARS2-AS1 Ensembl:ENSG00000231365 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1269714124 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557293 RMVar_hsa_circ_86930,RMVar_hsa_circ_135731 15946 RMVar_ID_15946 Human_SNP_ID_29683090 A-to-I Human chr1 + 119193409 119193409 119193409 TAACACAATTCTTATTTTACAGATAGAGAAATAGAAGCCATGTTGTTTGTGGAGGTTACACACTG TAACACAATTCTTATTTTACAGATAGAGAAATTGAAGCCATGTTGTTTGTGGAGGTTACACACTG A T WARS2-AS1 Ensembl:ENSG00000231365 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs962741086 Functional Loss SNV dbSNP153 33..33 33 - - - 15947 RMVar_ID_15947 Human_SNP_ID_29689868 A-to-I Human chr1 + 119223137 119223137 119223137 AGCTCAAATATTGGCCAGGAGCAGTGGCTCACACCTGTAATCCTAGCACTTTGGGAGACCAAGGC AGCTCAAATATTGGCCAGGAGCAGTGGCTCACGCCTGTAATCCTAGCACTTTGGGAGACCAAGGC A G WARS2-AS1 Ensembl:ENSG00000231365 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1211578848 Functional Loss SNV dbSNP153 33..33 33 - - - 15948 RMVar_ID_15948 Human_SNP_ID_29693987 A-to-I Human chr1 + 119242101 119242101 119242101 ACCTCGGGTGACCTGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGTGC ACCTCGGGTGACCTGCCCGCCTCGGCCTCCCAGAGTGCTGGGATTACAGGCATGAGCCACCGTGC A G WARS2-AS1 Ensembl:ENSG00000231365 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1233228126 Functional Loss SNV dbSNP153 33..33 33 - - - 15949 RMVar_ID_15949 Human_SNP_ID_29779272 A-to-I Human chr1 + 119567916 119567916 119567916 CACACAGAGCTCCAGAACAAGACCAAGCTGACAGTGCTGGAAGGAGACATTCTGGATGAGCCATT CACACAGAGCTCCAGAACAAGACCAAGCTGACGGTGCTGGAAGGAGACATTCTGGATGAGCCATT A G HSD3BP4 Ensembl:ENSG00000203855 Pseudogene exon GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs587645755 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_115118 15950 RMVar_ID_15950 Human_SNP_ID_29793125 A-to-I Human chr1 - 119620389 119620389 119620389 TCATCCAACTTTTGATTATTCATGGATTGATTATCCGCTTTTTTTTTGCTTTTTTGCTGCCATTG TCATCCAACTTTTGATTATTCATGGATTGATTTTCCGCTTTTTTTTTGCTTTTTTGCTGCCATTG T A ZNF697 Ensembl:ENSG00000143067 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs751500891 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5680111,Human_RBP_ID_24395205 RMVar_hsa_circ_107689,RMVar_hsa_circ_135735 15951 RMVar_ID_15951 Human_SNP_ID_82058026 A-to-I Human chr2 - 91623358 91623358 91623358 TCTCACTATGTTTGTGTTCCCTGGATGGTCTTAAACTCTTGGCCTCAAGCGATCCTTCTGTGTCA TCTCACTATGTTTGTGTTCCCTGGATGGTCTTCAACTCTTGGCCTCAAGCGATCCTTCTGTGTCA T G LSP1P4 Ensembl:ENSG00000143429 Pseudogene intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1292327297 Functional Loss SNV dbSNP153 33..33 33 - - - 15952 RMVar_ID_15952 Human_SNP_ID_82058075 A-to-I Human chr2 - 91623531 91623531 91623531 AGGGTCTTACTGTGCCACCCAAGCTAGAATGCAGTGGCACAATCTTGTCTCACTACCCAATCTCA AGGGTCTTACTGTGCCACCCAAGCTAGAATGCTGTGGCACAATCTTGTCTCACTACCCAATCTCA T A LSP1P4 Ensembl:ENSG00000143429 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1452479984 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8526908 15953 RMVar_ID_15953 Human_SNP_ID_82058078 A-to-I Human chr2 - 91623538 91623538 91623538 TAGAGACAGGGTCTTACTGTGCCACCCAAGCTAGAATGCAGTGGCACAATCTTGTCTCACTACCC TAGAGACAGGGTCTTACTGTGCCACCCAAGCTGGAATGCAGTGGCACAATCTTGTCTCACTACCC T C LSP1P4 Ensembl:ENSG00000143429 Pseudogene intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1355712749 Functional Loss SNV dbSNP153 33..33 33 - - - 15954 RMVar_ID_15954 Human_SNP_ID_82065224 A-to-I Human chr2 - 91645375 91645375 91645375 GAACTGAGATTGCGCCACTGCAATCTCAGCCTAGGAGACAGAGAGAGACGTCTCCTGTTCTCCTG GAACTGAGATTGCGCCACTGCAATCTCAGCCTGGGAGACAGAGAGAGACGTCTCCTGTTCTCCTG T C LSP1P4 Ensembl:ENSG00000143429 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs573533564 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101543,RMVar_hsa_circ_201774 15955 RMVar_ID_15955 Human_SNP_ID_82065609 A-to-I Human chr2 - 91646569 91646569 91646569 TCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGAGATTACAGGCACGCACCACCACACACG TCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTGGCTGAGATTACAGGCACGCACCACCACACACG T C LSP1P4 Ensembl:ENSG00000143429 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1186485631 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101543,RMVar_hsa_circ_201774 15956 RMVar_ID_15956 Human_SNP_ID_82067671 A-to-I Human chr2 - 91652826 91652823 91652826 TCTTGCTCTTGTTGCCCAGGCTGGAGTGCAGTAGTGGCATGATCTTGGCTCACCGCAACCTCCAC TCTTGCTCTTGTTGCCCAGGCTGGAGTGCAGT___GGCATGATCTTGGCTCACCGCAACCTCCAC CACT C LSP1P4 Ensembl:ENSG00000143429 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs3880378 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_101543,RMVar_hsa_circ_201774 15957 RMVar_ID_15957 Human_SNP_ID_82068606 A-to-I Human chr2 - 91655377 91655377 91655377 GAAGTACAGGCTCAGTCTGCGGCCAAGACTCCATCCTGCAAGGTAAGGTCCCCTCCAGGGGCAAG GAAGTACAGGCTCAGTCTGCGGCCAAGACTCCGTCCTGCAAGGTAAGGTCCCCTCCAGGGGCAAG T C LSP1P4 Ensembl:ENSG00000143429 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs112527890 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_918402,Human_RBP_ID_9384210,Human_RBP_ID_18999851 Human_Splice_Rec_272953,Human_Splice_Rec_272957,Human_Splice_Rec_272959,Human_Splice_Rec_272963,Human_Splice_Rec_272969,Human_Splice_Rec_272973 15958 RMVar_ID_15958 Human_SNP_ID_82068607 A-to-I Human chr2 - 91655377 91655377 91655377 GAAGTACAGGCTCAGTCTGCGGCCAAGACTCCATCCTGCAAGGTAAGGTCCCCTCCAGGGGCAAG GAAGTACAGGCTCAGTCTGCGGCCAAGACTCCCTCCTGCAAGGTAAGGTCCCCTCCAGGGGCAAG T G LSP1P4 Ensembl:ENSG00000143429 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs112527890 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_918402,Human_RBP_ID_9384210,Human_RBP_ID_18999851 Human_Splice_Rec_272953,Human_Splice_Rec_272957,Human_Splice_Rec_272959,Human_Splice_Rec_272963,Human_Splice_Rec_272969,Human_Splice_Rec_272973 15959 RMVar_ID_15959 Human_SNP_ID_83121712 A-to-I Human chr2 - 94769279 94769279 94769279 AAACTTCTACTAGGGCAGTGCGGAAGGAAAATATGGGGTTGGAGCCCCCACACTGGAGGTCACCA AAACTTCTACTAGGGCAGTGCGGAAGGAAAATGTGGGGTTGGAGCCCCCACACTGGAGGTCACCA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1181428728 Functional Loss SNV dbSNP153 33..33 33 - - - 15960 RMVar_ID_15960 Human_SNP_ID_83223835 A-to-I Human chr2 - 95121941 95121941 95121941 CGGGCTCCGCCTGCAGTGTGGCCCGTCCGGACAGTCCCTCACCCCGGCCTGCGCTGCTGCGTGGA CGGGCTCCGCCTGCAGTGTGGCCCGTCCGGACCGTCCCTCACCCCGGCCTGCGCTGCTGCGTGGA T G MRPS5 Ensembl:ENSG00000144029 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs766607274 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_557691,Human_RBP_ID_777170,Human_RBP_ID_4622538,Human_RBP_ID_5471149,Human_RBP_ID_8851993,Human_RBP_ID_9296667 15961 RMVar_ID_15961 Human_SNP_ID_83228898 A-to-I Human chr2 - 95145940 95145940 95145940 CCTGAGAACATGTGCCCAAGGTGGCTCTTGTCAGGAGCAGCAGCAGGTTGGGGCAGCCTAAAGAG CCTGAGAACATGTGCCCAAGGTGGCTCTTGTCGGGAGCAGCAGCAGGTTGGGGCAGCCTAAAGAG T C MRPS5,ZNF514 Ensembl:ENSG00000144029,Ensembl:ENSG00000144026 Protein coding,Protein coding intron,3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1434437433 Functional Loss SNV dbSNP153 33..33 33 - - - 15962 RMVar_ID_15962 Human_SNP_ID_83229059 A-to-I Human chr2 - 95146638 95146638 95146638 GTCCTGCCCTCCAAAAATCCTTTGCACGGCCTACAAGATAAATCCTCACCCCCCGTGTGTGGTAT GTCCTGCCCTCCAAAAATCCTTTGCACGGCCTGCAAGATAAATCCTCACCCCCCGTGTGTGGTAT T C MRPS5,ZNF514 Ensembl:ENSG00000144029,Ensembl:ENSG00000144026 Protein coding,Protein coding intron,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs533775913 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20610655 15963 RMVar_ID_15963 Human_SNP_ID_83358693 A-to-I Human chr2 - 95815881 95815881 95815881 TGTTTTTGTACCAGTATCATGCTGTTTTGGTTACTGTAGCCCTGTAGTATAGTTTGAAGTTGGGT TGTTTTTGTACCAGTATCATGCTGTTTTGGTTGCTGTAGCCCTGTAGTATAGTTTGAAGTTGGGT T C LINC00342 Ensembl:ENSG00000232931 lincRNA intron GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 29129909,30559470 RNA-Seq:(High) rs1207920495 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27016152 15964 RMVar_ID_15964 Human_SNP_ID_83360850 A-to-I Human chr2 - 95825193 95825186 95825193 GAGGTGGAGAAATCAATGCATTGGGTTAGAACATGCTCCTTTAGCTCTGTGAAATTTGTTATTAC GAGGTGGAGAAATCAATGCATTGGGTTAGAAC_______TTTAGCTCTGTGAAATTTGTTATTAC AGGAGCAT A LINC00342 Ensembl:ENSG00000232931 lincRNA intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1483702870 Functional Loss DEL dbSNP153 33..39 33 - - - 15965 RMVar_ID_15965 Human_SNP_ID_83360855 A-to-I Human chr2 - 95825206 95825206 95825206 CATCCCTGAAAGGGAGGTGGAGAAATCAATGCATTGGGTTAGAACATGCTCCTTTAGCTCTGTGA CATCCCTGAAAGGGAGGTGGAGAAATCAATGCGTTGGGTTAGAACATGCTCCTTTAGCTCTGTGA T C LINC00342 Ensembl:ENSG00000232931 lincRNA intron GSE107867 ASD brains,cerebellum;ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs997610179 Functional Loss SNV dbSNP153 33..33 33 - - - 15966 RMVar_ID_15966 Human_SNP_ID_83360916 A-to-I Human chr2 - 95825412 95825412 95825412 AGAAGTAGGCTTCAGAAGGTGGGTAGTAGCAAACTTCACTGAGCTAAAGGAGCACGTTCTAACCC AGAAGTAGGCTTCAGAAGGTGGGTAGTAGCAATCTTCACTGAGCTAAAGGAGCACGTTCTAACCC T A LINC00342 Ensembl:ENSG00000232931 lincRNA intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1250661853 Functional Loss SNV dbSNP153 33..33 33 - - - 15967 RMVar_ID_15967 Human_SNP_ID_83361811 A-to-I Human chr2 - 95829975 95829975 95829975 CTTTAAGAAGGTCCCCAATCCCATTCCTCCTCACTGGGCAGGACCTCCCAACCAGGGCCTGTAGC CTTTAAGAAGGTCCCCAATCCCATTCCTCCTCTCTGGGCAGGACCTCCCAACCAGGGCCTGTAGC T A LINC00342 Ensembl:ENSG00000232931 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs148556344 Functional Loss SNV dbSNP153 33..33 33 - - - 15968 RMVar_ID_15968 Human_SNP_ID_83362023 A-to-I Human chr2 - 95831104 95831104 95831104 ACTGTATTGACTTGCTCCTTTCATTCCTCTCCATGAGAGCCGTGCACCCTACCTGCTTCTAGTCA ACTGTATTGACTTGCTCCTTTCATTCCTCTCCGTGAGAGCCGTGCACCCTACCTGCTTCTAGTCA T C LINC00342 Ensembl:ENSG00000232931 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1185748829 Functional Loss SNV dbSNP153 33..33 33 - - - 15969 RMVar_ID_15969 Human_SNP_ID_83362029 A-to-I Human chr2 - 95831136 95831136 95831136 AATGCGAGTACCTGGTTGTTTCAGTTGAAGGTACTGTATTGACTTGCTCCTTTCATTCCTCTCCA AATGCGAGTACCTGGTTGTTTCAGTTGAAGGTGCTGTATTGACTTGCTCCTTTCATTCCTCTCCA T C LINC00342 Ensembl:ENSG00000232931 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs189274894 Functional Loss SNV dbSNP153 33..33 33 - - - 15970 RMVar_ID_15970 Human_SNP_ID_83362153 A-to-I Human chr2 - 95831639 95831639 95831639 ACGGATCGGGGATCTACTTAAAGGATCTTGCCATGATTTGGTAGAGCAGTTGTGCTGTTCTGGGG ACGGATCGGGGATCTACTTAAAGGATCTTGCCTTGATTTGGTAGAGCAGTTGTGCTGTTCTGGGG T A LINC00342 Ensembl:ENSG00000232931 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1475775522 Functional Loss SNV dbSNP153 33..33 33 - - - 15971 RMVar_ID_15971 Human_SNP_ID_83362167 A-to-I Human chr2 - 95831703 95831703 95831703 AATCTCTGTCAGCTCTAGAACTAAGAGGTGGAAGCCCCACTTGGGAGGTCTCACCCAATGAGGAA AATCTCTGTCAGCTCTAGAACTAAGAGGTGGAGGCCCCACTTGGGAGGTCTCACCCAATGAGGAA T C LINC00342 Ensembl:ENSG00000232931 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1220136246 Functional Loss SNV dbSNP153 33..33 33 - - - 15972 RMVar_ID_15972 Human_SNP_ID_83362441 A-to-I Human chr2 - 95832926 95832926 95832926 CCACCGGTGTTCTCGGGCTGACAGAGATCTGAATTCTCCCTGGCATGTAGTTCTCAAGGTCCCAC CCACCGGTGTTCTCGGGCTGACAGAGATCTGATTTCTCCCTGGCATGTAGTTCTCAAGGTCCCAC T A LINC00342 Ensembl:ENSG00000232931 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs990011544 Functional Loss SNV dbSNP153 33..33 33 - - - 15973 RMVar_ID_15973 Human_SNP_ID_83363396 A-to-I Human chr2 - 95835709 95835709 95835709 AGCTGAAAGGACCCTCATTGAGCTGGACCTCCAGGCCTCCATGCCAGGGAGAACTCAAATCTCTG AGCTGAAAGGACCCTCATTGAGCTGGACCTCCGGGCCTCCATGCCAGGGAGAACTCAAATCTCTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1430817250 Functional Loss SNV dbSNP153 33..33 33 - - - 15974 RMVar_ID_15974 Human_SNP_ID_83363442 A-to-I Human chr2 - 95835833 95835833 95835833 GGGCTGTAACGACTAAGTTGCACAAACAGCAAAGATAGCTCCTTGCTCCTGCGCGTGGGAACTCA GGGCTGTAACGACTAAGTTGCACAAACAGCAAGGATAGCTCCTTGCTCCTGCGCGTGGGAACTCA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1391230196 Functional Loss SNV dbSNP153 33..33 33 - - - 15975 RMVar_ID_15975 Human_SNP_ID_83409601 A-to-I Human chr2 + 96012679 96012679 96012679 GCTGGTCTTGAACTCCTGACCTCAAGTGATCCACCCACCTCGAACTCCCAATGTGCTAGGGATTT GCTGGTCTTGAACTCCTGACCTCAAGTGATCCTCCCACCTCGAACTCCCAATGTGCTAGGGATTT A T FAHD2CP Ensembl:ENSG00000231584 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1386744506 Functional Loss SNV dbSNP153 33..33 33 - - - 15976 RMVar_ID_15976 Human_SNP_ID_83448527 A-to-I Human chr2 - 96188055 96188055 96188055 GCCAGGCTGGTCTCGAACTCTGGTCCTCAAGTAATCTGCCTGCCTTGGGCTCCCAAAGTGCTGGG GCCAGGCTGGTCTCGAACTCTGGTCCTCAAGTTATCTGCCTGCCTTGGGCTCCCAAAGTGCTGGG T A STARD7 Ensembl:ENSG00000084090 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1189524290 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25571508 RMVar_hsa_circ_201830,RMVar_hsa_circ_119875,RMVar_hsa_circ_267804 15977 RMVar_ID_15977 Human_SNP_ID_83448550 A-to-I Human chr2 - 96188163 96188163 96188163 CAAACGATTCTCCTGCCTCAGACTCCCAAGTAACTGGGATTACAGGCGTGTACCACCACGCCCAG CAAACGATTCTCCTGCCTCAGACTCCCAAGTAGCTGGGATTACAGGCGTGTACCACCACGCCCAG T C STARD7 Ensembl:ENSG00000084090 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1269701905 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_201830,RMVar_hsa_circ_119875,RMVar_hsa_circ_267804 15978 RMVar_ID_15978 Human_SNP_ID_83448569 A-to-I Human chr2 - 96188228 96188228 96188228 GTCTGTCACCCAGGCTGGAGTACAGTGGCTCAATCTGTGCTCACTGCAACCTCTGCCTCCCGGTT GTCTGTCACCCAGGCTGGAGTACAGTGGCTCAGTCTGTGCTCACTGCAACCTCTGCCTCCCGGTT T C STARD7 Ensembl:ENSG00000084090 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs564069907 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_201830,RMVar_hsa_circ_119875,RMVar_hsa_circ_267804 15979 RMVar_ID_15979 Human_SNP_ID_83448684 A-to-I Human chr2 - 96188526 96188526 96188526 ACACGCTTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGTGGATCACTTGAGGTCGGGAGTTCG ACACGCTTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGTGGATCACTTGAGGTCGGGAGTTCG T C STARD7 Ensembl:ENSG00000084090 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs535044579 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_201830,RMVar_hsa_circ_119875,RMVar_hsa_circ_267804 15980 RMVar_ID_15980 Human_SNP_ID_83448685 A-to-I Human chr2 - 96188526 96188526 96188526 ACACGCTTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGTGGATCACTTGAGGTCGGGAGTTCG ACACGCTTGTAATCCCAGCACTTTGGGAGGCCCAGGTGGGTGGATCACTTGAGGTCGGGAGTTCG T G STARD7 Ensembl:ENSG00000084090 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs535044579 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_201830,RMVar_hsa_circ_119875,RMVar_hsa_circ_267804 15981 RMVar_ID_15981 Human_SNP_ID_83448901 A-to-I Human chr2 - 96189221 96189221 96189221 ACTCTGGCTGAGCACGGTAGCTCATGCCTGTAATCGCAGCACTTTGGGAGGCTGAGGCAGGAGGA ACTCTGGCTGAGCACGGTAGCTCATGCCTGTAGTCGCAGCACTTTGGGAGGCTGAGGCAGGAGGA T C STARD7 Ensembl:ENSG00000084090 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1294393669 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_201830,RMVar_hsa_circ_119875,RMVar_hsa_circ_267804 15982 RMVar_ID_15982 Human_SNP_ID_83456008 A-to-I Human chr2 + 96215634 96215634 96215634 TGGAGTGCGGTGGCTTGATCTTGCCTCACTGCAACCTCTGGCACCCGAGTTTAAGCGATTCTCCT TGGAGTGCGGTGGCTTGATCTTGCCTCACTGCCACCTCTGGCACCCGAGTTTAAGCGATTCTCCT A C STARD7-AS1 Ensembl:ENSG00000204685 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs936500820 Functional Loss SNV dbSNP153 33..33 33 - - - 15983 RMVar_ID_15983 Human_SNP_ID_83456013 A-to-I Human chr2 + 96215649 96215649 96215649 TGATCTTGCCTCACTGCAACCTCTGGCACCCGAGTTTAAGCGATTCTCCTGCCTCAGCCTCTGAA TGATCTTGCCTCACTGCAACCTCTGGCACCCGTGTTTAAGCGATTCTCCTGCCTCAGCCTCTGAA A T STARD7-AS1 Ensembl:ENSG00000204685 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1331532811 Functional Loss SNV dbSNP153 33..33 33 - - - 15984 RMVar_ID_15984 Human_SNP_ID_83462345 A-to-I Human chr2 + 96243446 96243446 96243446 GCACACCTGTAGTCCCAGCAACCTGGAGGCTGAAGTGTGAGGATTGCTTAAACCTAAGGAGATAG GCACACCTGTAGTCCCAGCAACCTGGAGGCTGCAGTGTGAGGATTGCTTAAACCTAAGGAGATAG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042210270 Functional Loss SNV dbSNP153 33..33 33 - - - 15985 RMVar_ID_15985 Human_SNP_ID_83463711 A-to-I Human chr2 - 96249160 96249160 96249160 CCGGGAGGCAGAGGTTGCAGTGAGCCGAGATCATGCCACTGGACTCCAGCCTGACAGAGTGAGAC CCGGGAGGCAGAGGTTGCAGTGAGCCGAGATCGTGCCACTGGACTCCAGCCTGACAGAGTGAGAC T C TMEM127 Ensembl:ENSG00000135956 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1445742877 Functional Loss SNV dbSNP153 33..33 33 - - - 15986 RMVar_ID_15986 Human_SNP_ID_83463762 A-to-I Human chr2 - 96249371 96249371 96249371 TCAGTTCTGGCCGGGTGCGGTGGCTCACGCCTATTATCCCAGCACTTTGGGAGGCCGAGGTGGGT TCAGTTCTGGCCGGGTGCGGTGGCTCACGCCTGTTATCCCAGCACTTTGGGAGGCCGAGGTGGGT T C TMEM127 Ensembl:ENSG00000135956 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs540102298 Functional Loss SNV dbSNP153 33..33 33 - - - 15987 RMVar_ID_15987 Human_SNP_ID_83469205 A-to-I Human chr2 + 96270645 96270645 96270645 CAGCCTGTCCAATGTGATAAAACCCTGTCTCTACTGAAAATACAAAAATTAGCCGGGCATGGTGG CAGCCTGTCCAATGTGATAAAACCCTGTCTCTGCTGAAAATACAAAAATTAGCCGGGCATGGTGG A G CIAO1 Ensembl:ENSG00000144021 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1273012787 Functional Loss SNV dbSNP153 33..33 33 - - - 15988 RMVar_ID_15988 Human_SNP_ID_83471945 A-to-I Human chr2 - 96280454 96280454 96280454 TTGTTCTGTCGTTTAGGCTGGAATGCGGTGGTATGATCTCAGCCCACTACAGCCTCTGCCTGCCA TTGTTCTGTCGTTTAGGCTGGAATGCGGTGGTGTGATCTCAGCCCACTACAGCCTCTGCCTGCCA T C SNRNP200 Ensembl:ENSG00000144028 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1033570823 Functional Loss SNV dbSNP153 33..33 33 - - - 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_83181,RMVar_hsa_circ_84227,RMVar_hsa_circ_94313,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_126625,RMVar_hsa_circ_201851,RMVar_hsa_circ_106112,RMVar_hsa_circ_201853,RMVar_hsa_circ_266002,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_201858,RMVar_hsa_circ_201859 15989 RMVar_ID_15989 Human_SNP_ID_83492311 A-to-I Human chr2 + 96361902 96361902 96361902 CTATTTGTTTTTTTGTATTTTTTTTTAGAGACAGGGTCTTGCTCTGTTGCCCAGGCCATAGTCCA CTATTTGTTTTTTTGTATTTTTTTTTAGAGACGGGGTCTTGCTCTGTTGCCCAGGCCATAGTCCA A G NCAPH Ensembl:ENSG00000121152 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924970269 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13989100 RMVar_hsa_circ_12734,RMVar_hsa_circ_20526,RMVar_hsa_circ_201878,RMVar_hsa_circ_9410,RMVar_hsa_circ_332299,RMVar_hsa_circ_369827,RMVar_hsa_circ_375728,RMVar_hsa_circ_201880,RMVar_hsa_circ_201879,RMVar_hsa_circ_201885,RMVar_hsa_circ_331537,RMVar_hsa_circ_373342,RMVar_hsa_circ_307435,RMVar_hsa_circ_201884,RMVar_hsa_circ_34278,RMVar_hsa_circ_334020 15990 RMVar_ID_15990 Human_SNP_ID_83554945 A-to-I Human chr2 - 96614711 96614711 96614711 GCTGGAGTGCAGTGTCATGACCTTGGCTCACCACAACCTCCACCTCCCGGGTTCAGGTGATTCTC GCTGGAGTGCAGTGTCATGACCTTGGCTCACCGCAACCTCCACCTCCCGGGTTCAGGTGATTCTC T C KANSL3 Ensembl:ENSG00000114982 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1169600534 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25572100 RMVar_hsa_circ_22302,RMVar_hsa_circ_330416,RMVar_hsa_circ_326447,RMVar_hsa_circ_71522,RMVar_hsa_circ_201888,RMVar_hsa_circ_104734,RMVar_hsa_circ_290987,RMVar_hsa_circ_375483,RMVar_hsa_circ_28525,RMVar_hsa_circ_21327,RMVar_hsa_circ_54551,RMVar_hsa_circ_201889,RMVar_hsa_circ_201890,RMVar_hsa_circ_105854,RMVar_hsa_circ_268934,RMVar_hsa_circ_201891,RMVar_hsa_circ_372706,RMVar_hsa_circ_88648,RMVar_hsa_circ_46070,RMVar_hsa_circ_201892,RMVar_hsa_circ_201893,RMVar_hsa_circ_59303,RMVar_hsa_circ_201895,RMVar_hsa_circ_201897,RMVar_hsa_circ_370146 15991 RMVar_ID_15991 Human_SNP_ID_83559056 A-to-I Human chr2 - 96632633 96632633 96632633 CTTTTCTCCATTTGTACTGTTCTTGTCCCTAAACGAGCTCTCATGATTTCTGGCCCATCTCAGTC CTTTTCTCCATTTGTACTGTTCTTGTCCCTAATCGAGCTCTCATGATTTCTGGCCCATCTCAGTC T A KANSL3 Ensembl:ENSG00000114982 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1057381852 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_326447,RMVar_hsa_circ_372706,RMVar_hsa_circ_88648,RMVar_hsa_circ_201892,RMVar_hsa_circ_201893 15992 RMVar_ID_15992 Human_SNP_ID_83559057 A-to-I Human chr2 - 96632634 96632634 96632634 ACTTTTCTCCATTTGTACTGTTCTTGTCCCTAAACGAGCTCTCATGATTTCTGGCCCATCTCAGT ACTTTTCTCCATTTGTACTGTTCTTGTCCCTAGACGAGCTCTCATGATTTCTGGCCCATCTCAGT T C KANSL3 Ensembl:ENSG00000114982 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs188040142 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13990947 RMVar_hsa_circ_326447,RMVar_hsa_circ_372706,RMVar_hsa_circ_88648,RMVar_hsa_circ_201892,RMVar_hsa_circ_201893 15993 RMVar_ID_15993 Human_SNP_ID_83559700 A-to-I Human chr2 - 96635060 96635060 96635060 ACTGAGATGGGCCAGAAATCGTGATATCTTGTATAGGGCAGGAACAGTACAAATGGAGAAATATA ACTGAGATGGGCCAGAAATCGTGATATCTTGTGTAGGGCAGGAACAGTACAAATGGAGAAATATA T C KANSL3 Ensembl:ENSG00000114982 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs778714015 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13991072,Human_RBP_ID_25592482 RMVar_hsa_circ_326447,RMVar_hsa_circ_372706,RMVar_hsa_circ_88648,RMVar_hsa_circ_201892,RMVar_hsa_circ_201893 15994 RMVar_ID_15994 Human_SNP_ID_83561904 A-to-I Human chr2 + 96643449 96643449 96643449 TCGGCTCACTGCAACCTCTGCCTCCCAGGTTCAAGCAATTCTCCTGCCTCACCCTCCGAAGTAGC TCGGCTCACTGCAACCTCTGCCTCCCAGGTTCCAGCAATTCTCCTGCCTCACCCTCCGAAGTAGC A C FER1L5 Ensembl:ENSG00000249715 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1284982703 Functional Loss SNV dbSNP153 33..33 33 - - - 15995 RMVar_ID_15995 Human_SNP_ID_83564847 A-to-I Human chr2 + 96654805 96654805 96654805 CCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAACCCAGGAGGCGGAGCTT CCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCGGGAGAATTGCTTGAACCCAGGAGGCGGAGCTT A G FER1L5 Ensembl:ENSG00000249715 Protein coding exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1395941586 Functional Loss SNV dbSNP153 33..33 33 - - - 15996 RMVar_ID_15996 Human_SNP_ID_83582574 A-to-I Human chr2 - 96721487 96721487 96721487 AAAAAAACAAAGTAGGAGTAATTGCCAGGCACAGTGGCTTACACTTGTAATTCTAGCACTTTAGG AAAAAAACAAAGTAGGAGTAATTGCCAGGCACGGTGGCTTACACTTGTAATTCTAGCACTTTAGG T C LMAN2L Ensembl:ENSG00000114988 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928206637 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_376713,RMVar_hsa_circ_334130,RMVar_hsa_circ_36375,RMVar_hsa_circ_201901 15997 RMVar_ID_15997 Human_SNP_ID_83582633 A-to-I Human chr2 - 96721683 96721683 96721683 TTGAGTCTAGGAGTTTTAGATCAGCTTGGGCAACATAGGGAGACCCCATCTTTACAAAAAACAAA TTGAGTCTAGGAGTTTTAGATCAGCTTGGGCAGCATAGGGAGACCCCATCTTTACAAAAAACAAA T C LMAN2L Ensembl:ENSG00000114988 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs966780949 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_376713,RMVar_hsa_circ_334130,RMVar_hsa_circ_36375,RMVar_hsa_circ_201901 15998 RMVar_ID_15998 Human_SNP_ID_83584453 A-to-I Human chr2 - 96728914 96728914 96728914 CCCACCTTAGCCTCCCAAAATGCTGAGATTACAGGGGTGAGCCACTGCGCCTGGCCTTATTTTAT CCCACCTTAGCCTCCCAAAATGCTGAGATTACCGGGGTGAGCCACTGCGCCTGGCCTTATTTTAT T G LMAN2L Ensembl:ENSG00000114988 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1186368295 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_376713,RMVar_hsa_circ_334130,RMVar_hsa_circ_36375,RMVar_hsa_circ_201901 15999 RMVar_ID_15999 Human_SNP_ID_83604157 A-to-I Human chr2 + 96807088 96807088 96807088 GACAGAGTGTAGTGGTACAATCTCGGCTCGTTACAACCTCCGCCTCCCAGGCTCAGGTGACCCTC GACAGAGTGTAGTGGTACAATCTCGGCTCGTTGCAACCTCCGCCTCCCAGGCTCAGGTGACCCTC A G CNNM4 Ensembl:ENSG00000158158 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1271607031 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_364572,RMVar_hsa_circ_201906,RMVar_hsa_circ_370820 16000 RMVar_ID_16000 Human_SNP_ID_83609375 A-to-I Human chr2 - 96825659 96825657 96825659 CGATCTCGTGATCTGCCTGCCTGGGCCTCCCAAAGAGCTGGGATTACAGGCGTGAGCCACTGCGC CGATCTCGTGATCTGCCTGCCTGGGCCTCCCA__GAGCTGGGATTACAGGCGTGAGCCACTGCGC CTT C ANKRD23 Ensembl:ENSG00000163126 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 29129909,30559470 RNA-Seq:(High) rs1258742607 Functional Loss DEL dbSNP153 33..34 33 - - - 16001 RMVar_ID_16001 Human_SNP_ID_83609394 A-to-I Human chr2 - 96825735 96825735 96825735 CACCACGCCCAGCTAATGTTTGTATTTTTAGCAGAGATGGAGTTTCACCATATTGGCCAGGCTGG CACCACGCCCAGCTAATGTTTGTATTTTTAGCGGAGATGGAGTTTCACCATATTGGCCAGGCTGG T C ANKRD23 Ensembl:ENSG00000163126 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444094513 Functional Loss SNV dbSNP153 33..33 33 - - - 16002 RMVar_ID_16002 Human_SNP_ID_83609421 A-to-I Human chr2 - 96825777 96825777 96825777 TCTGCCTCAGCCTCCTGAGTATGTGAGACTACAGGCACGCACCACCACGCCCAGCTAATGTTTGT TCTGCCTCAGCCTCCTGAGTATGTGAGACTACCGGCACGCACCACCACGCCCAGCTAATGTTTGT T G ANKRD23 Ensembl:ENSG00000163126 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1371303044 Functional Loss SNV dbSNP153 33..33 33 - - - 16003 RMVar_ID_16003 Human_SNP_ID_83609564 A-to-I Human chr2 - 96826310 96826310 96826310 TGCTCAGGAGGCTGAGGTGGGAGGAACACTTGAGTCTGGGAAGTTGAGGCTGCAGTAAGCCATGA TGCTCAGGAGGCTGAGGTGGGAGGAACACTTGTGTCTGGGAAGTTGAGGCTGCAGTAAGCCATGA T A ANKRD23 Ensembl:ENSG00000163126 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1227495449 Functional Loss SNV dbSNP153 33..33 33 - - - 16004 RMVar_ID_16004 Human_SNP_ID_83616406 A-to-I Human chr2 - 96849307 96849307 96849307 AATTATTTTTTAAAAAAAGGTTAGCCACGTGTAGTGGTGCACGCCTGCAATCTCAGCTACTTGGG AATTATTTTTTAAAAAAAGGTTAGCCACGTGTGGTGGTGCACGCCTGCAATCTCAGCTACTTGGG T C ANKRD39,ANKRD23 Ensembl:ENSG00000213337,Ensembl:ENSG00000163126 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1363482878 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36388,RMVar_hsa_circ_23182 16005 RMVar_ID_16005 Human_SNP_ID_83622923 A-to-I Human chr2 + 96871573 96871573 96871573 ACCCTTTAAAAAGTAAGTAATTTGGGAGGCTGAGATGGGAGGATCACTTGACCCCAGGAGTTCAA ACCCTTTAAAAAGTAAGTAATTTGGGAGGCTGCGATGGGAGGATCACTTGACCCCAGGAGTTCAA A C lnc-CNNM3-3,lnc-CNNM3-3:2 RNACentral:URS00008BC94C,RNACentral:URS00009AE1D6 lincRNA,lincRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs546443582 Functional Loss SNV dbSNP153 33..33 33 - - - 16006 RMVar_ID_16006 Human_SNP_ID_83623159 A-to-I Human chr2 + 96872408 96872408 96872408 TGGTGGCATGCATCTGTAAGTCCCAGCTACTCAGGAGGCTGGAGTGGGAGGGTCGCTTGAGCCCA TGGTGGCATGCATCTGTAAGTCCCAGCTACTCTGGAGGCTGGAGTGGGAGGGTCGCTTGAGCCCA A T lnc-CNNM3-3,lnc-CNNM3-3:2 RNACentral:URS0000D5B68F,RNACentral:URS00008BC94C lincRNA,lincRNA exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1010026762 Functional Loss SNV dbSNP153 33..33 33 - - - 16007 RMVar_ID_16007 Human_SNP_ID_83623271 A-to-I Human chr2 + 96872854 96872847 96872854 ACACCATCATACACGGGACAGGGTCTCGCTATATTGCTCAGACTGGAAAGTTCAGATTTTTAAAT ACACCATCATACACGGGACAGGGTCT_______TTGCTCAGACTGGAAAGTTCAGATTTTTAAAT TCGCTATA T lnc-CNNM3-3,lnc-CNNM3-3:2 RNACentral:URS0000D5B68F,RNACentral:URS00008BC94C lincRNA,lincRNA exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1396572521 Functional Loss DEL dbSNP153 27..33 33 - - - 16008 RMVar_ID_16008 Human_SNP_ID_83623277 A-to-I Human chr2 + 96872854 96872852 96872855 ACACCATCATACACGGGACAGGGTCTCGCTATATTGCTCAGACTGGAAAGTTCAGATTTTTAAAT ACACCATCATACACGGGACAGGGTCTCGCTA___TGCTCAGACTGGAAAGTTCAGATTTTTAAAT ATAT A lnc-CNNM3-3,lnc-CNNM3-3:2 RNACentral:URS0000D5B68F,RNACentral:URS00008BC94C lincRNA,lincRNA exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1203936856 Functional Loss DEL dbSNP153 32..34 33 - - - 16009 RMVar_ID_16009 Human_SNP_ID_83696259 A-to-I Human chr2 + 97163607 97163607 97163607 TTTTCTTTTCTTTTTTTTTGAGACGGAGTCTCACTCTGTCACCCAGGCTTGAGTGCAGTGGCGGG TTTTCTTTTCTTTTTTTTTGAGACGGAGTCTCCCTCTGTCACCCAGGCTTGAGTGCAGTGGCGGG A C ANKRD36 Ensembl:ENSG00000135976 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs796877066 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42468,RMVar_hsa_circ_50477,RMVar_hsa_circ_113791,RMVar_hsa_circ_126361,RMVar_hsa_circ_269095,RMVar_hsa_circ_201946,RMVar_hsa_circ_376955,RMVar_hsa_circ_266877,RMVar_hsa_circ_123640,RMVar_hsa_circ_266609,RMVar_hsa_circ_201947,RMVar_hsa_circ_267740,RMVar_hsa_circ_266482,RMVar_hsa_circ_87164,RMVar_hsa_circ_201949,RMVar_hsa_circ_201950,RMVar_hsa_circ_265246,RMVar_hsa_circ_2120,RMVar_hsa_circ_80909,RMVar_hsa_circ_85878,RMVar_hsa_circ_111867,RMVar_hsa_circ_201954,RMVar_hsa_circ_201955,RMVar_hsa_circ_122858,RMVar_hsa_circ_112864,RMVar_hsa_circ_201957,RMVar_hsa_circ_201958,RMVar_hsa_circ_345094,RMVar_hsa_circ_310489,RMVar_hsa_circ_201959,RMVar_hsa_circ_201960,RMVar_hsa_circ_53007 16010 RMVar_ID_16010 Human_SNP_ID_83696260 A-to-I Human chr2 + 97163607 97163607 97163607 TTTTCTTTTCTTTTTTTTTGAGACGGAGTCTCACTCTGTCACCCAGGCTTGAGTGCAGTGGCGGG TTTTCTTTTCTTTTTTTTTGAGACGGAGTCTCGCTCTGTCACCCAGGCTTGAGTGCAGTGGCGGG A G ANKRD36 Ensembl:ENSG00000135976 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs796877066 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42468,RMVar_hsa_circ_50477,RMVar_hsa_circ_113791,RMVar_hsa_circ_126361,RMVar_hsa_circ_269095,RMVar_hsa_circ_201946,RMVar_hsa_circ_376955,RMVar_hsa_circ_266877,RMVar_hsa_circ_123640,RMVar_hsa_circ_266609,RMVar_hsa_circ_201947,RMVar_hsa_circ_267740,RMVar_hsa_circ_266482,RMVar_hsa_circ_87164,RMVar_hsa_circ_201949,RMVar_hsa_circ_201950,RMVar_hsa_circ_265246,RMVar_hsa_circ_2120,RMVar_hsa_circ_80909,RMVar_hsa_circ_85878,RMVar_hsa_circ_111867,RMVar_hsa_circ_201954,RMVar_hsa_circ_201955,RMVar_hsa_circ_122858,RMVar_hsa_circ_112864,RMVar_hsa_circ_201957,RMVar_hsa_circ_201958,RMVar_hsa_circ_345094,RMVar_hsa_circ_310489,RMVar_hsa_circ_201959,RMVar_hsa_circ_201960,RMVar_hsa_circ_53007 16011 RMVar_ID_16011 Human_SNP_ID_83696261 A-to-I Human chr2 + 97163607 97163607 97163607 TTTTCTTTTCTTTTTTTTTGAGACGGAGTCTCACTCTGTCACCCAGGCTTGAGTGCAGTGGCGGG TTTTCTTTTCTTTTTTTTTGAGACGGAGTCTCTCTCTGTCACCCAGGCTTGAGTGCAGTGGCGGG A T ANKRD36 Ensembl:ENSG00000135976 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs796877066 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42468,RMVar_hsa_circ_50477,RMVar_hsa_circ_113791,RMVar_hsa_circ_126361,RMVar_hsa_circ_269095,RMVar_hsa_circ_201946,RMVar_hsa_circ_376955,RMVar_hsa_circ_266877,RMVar_hsa_circ_123640,RMVar_hsa_circ_266609,RMVar_hsa_circ_201947,RMVar_hsa_circ_267740,RMVar_hsa_circ_266482,RMVar_hsa_circ_87164,RMVar_hsa_circ_201949,RMVar_hsa_circ_201950,RMVar_hsa_circ_265246,RMVar_hsa_circ_2120,RMVar_hsa_circ_80909,RMVar_hsa_circ_85878,RMVar_hsa_circ_111867,RMVar_hsa_circ_201954,RMVar_hsa_circ_201955,RMVar_hsa_circ_122858,RMVar_hsa_circ_112864,RMVar_hsa_circ_201957,RMVar_hsa_circ_201958,RMVar_hsa_circ_345094,RMVar_hsa_circ_310489,RMVar_hsa_circ_201959,RMVar_hsa_circ_201960,RMVar_hsa_circ_53007 16012 RMVar_ID_16012 Human_SNP_ID_83710202 A-to-I Human chr2 - 97204202 97204202 97204202 CCTCTGGCTATATTCAAAACAGAATCTTTCTCATCACTTGTAGCCTGAATGGAATTTGAAATGAA CCTCTGGCTATATTCAAAACAGAATCTTTCTCGTCACTTGTAGCCTGAATGGAATTTGAAATGAA T C - - Other Unknown GSE107867 ASD brains,frontal_cortex;ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs553334409 Functional Loss SNV dbSNP153 33..33 33 - - - 16013 RMVar_ID_16013 Human_SNP_ID_83711018 A-to-I Human chr2 - 97206074 97206074 97206074 TCTCTGGCTATACTCAAAACAGAATCTTCCTCATCACTTGTAGCCTGAATGGAATTTGAAACAAA TCTCTGGCTATACTCAAAACAGAATCTTCCTCGTCACTTGTAGCCTGAATGGAATTTGAAACAAA T C - - Other Unknown GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs771135449 Functional Loss SNV dbSNP153 33..33 33 - - - 16014 RMVar_ID_16014 Human_SNP_ID_83711019 A-to-I Human chr2 - 97206074 97206074 97206074 TCTCTGGCTATACTCAAAACAGAATCTTCCTCATCACTTGTAGCCTGAATGGAATTTGAAACAAA TCTCTGGCTATACTCAAAACAGAATCTTCCTCCTCACTTGTAGCCTGAATGGAATTTGAAACAAA T G - - Other Unknown GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs771135449 Functional Loss SNV dbSNP153 33..33 33 - - - 16015 RMVar_ID_16015 Human_SNP_ID_83714034 A-to-I Human chr2 + 97213554 97213554 97213554 TTGTTTCAAATTCCATTCAGGCTACAAGTGACAAGAAAGATTCTGTTTCGAATATACCCACAGAA TTGTTTCAAATTCCATTCAGGCTACAAGTGACGAGAAAGATTCTGTTTCGAATATACCCACAGAA A G ANKRD36 Ensembl:ENSG00000135976 Protein coding CDS GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1393443029 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_276964,Human_Splice_Rec_276965,Human_Splice_Rec_277114,Human_Splice_Rec_277115,Human_Splice_Rec_277276,Human_Splice_Rec_277277,Human_Splice_Rec_277340,Human_Splice_Rec_277341 RMVar_hsa_circ_80909,RMVar_hsa_circ_122858,RMVar_hsa_circ_201957,RMVar_hsa_circ_201958,RMVar_hsa_circ_345094,RMVar_hsa_circ_75958,RMVar_hsa_circ_201961,RMVar_hsa_circ_346161,RMVar_hsa_circ_269254,RMVar_hsa_circ_50808,RMVar_hsa_circ_267344,RMVar_hsa_circ_47725,RMVar_hsa_circ_269555,RMVar_hsa_circ_268927,RMVar_hsa_circ_265517,RMVar_hsa_circ_265295,RMVar_hsa_circ_41705,RMVar_hsa_circ_265289,RMVar_hsa_circ_268294,RMVar_hsa_circ_9800,RMVar_hsa_circ_101525,RMVar_hsa_circ_108848,RMVar_hsa_circ_325449,RMVar_hsa_circ_201972,RMVar_hsa_circ_85711,RMVar_hsa_circ_201973,RMVar_hsa_circ_201971 16016 RMVar_ID_16016 Human_SNP_ID_83738636 A-to-I Human chr2 - 97490250 97490250 97490250 CCATGGCCTCCAGCCACCCCCGCTGGTGTTCCAGGGCTGACAGAGATCTGAATTCTCCCTGGCAC CCATGGCCTCCAGCCACCCCCGCTGGTGTTCCGGGGCTGACAGAGATCTGAATTCTCCCTGGCAC T C NONHSAG028655.2-001 RNACentral:URS00009B5FB3 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1302554068 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23183348 16017 RMVar_ID_16017 Human_SNP_ID_83738653 A-to-I Human chr2 - 97490311 97490308 97490312 GAGATTTGAATTCTCCCTGCCATGAAGGCCTCAGGGTCTGGCCCAGTGAGGGACCTCCCAACCAT GAGATTTGAATTCTCCCTGCCATGAAGGCCT____GTCTGGCCCAGTGAGGGACCTCCCAACCAT CCCTG C NONHSAG028655.2-001 RNACentral:URS00009B5FB3 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1312431199 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_23183350 16018 RMVar_ID_16018 Human_SNP_ID_83738655 A-to-I Human chr2 - 97490311 97490309 97490311 GAGATTTGAATTCTCCCTGCCATGAAGGCCTCAGGGTCTGGCCCAGTGAGGGACCTCCCAACCAT GAGATTTGAATTCTCCCTGCCATGAAGGCCTC__GGTCTGGCCCAGTGAGGGACCTCCCAACCAT CCT C NONHSAG028655.2-001 RNACentral:URS00009B5FB3 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1559086960 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_23183350 16019 RMVar_ID_16019 Human_SNP_ID_83772699 A-to-I Human chr2 - 97659386 97659386 97659386 GAACGACATGGAACGCATCTGGCAGTACGTCTACTCCAAGGATCAGCTGCAGACCTTCTCGGAGG GAACGACATGGAACGCATCTGGCAGTACGTCTGCTCCAAGGATCAGCTGCAGACCTTCTCGGAGG T C ACTR1B Ensembl:ENSG00000115073 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs747815293 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_558457,Human_RBP_ID_920671,Human_RBP_ID_1592007,Human_RBP_ID_1925562,Human_RBP_ID_3959395,Human_RBP_ID_9387096,Human_RBP_ID_19002257,Human_RBP_ID_22997013,Human_RBP_ID_23890673 Human_Splice_Rec_277916,Human_Splice_Rec_277917,Human_Splice_Rec_277936,Human_Splice_Rec_277937,Human_Splice_Rec_277943 Human_miRNA_ID_2011429,Human_miRNA_ID_2489576,Human_miRNA_ID_2584736,Human_miRNA_ID_2614403,Human_miRNA_ID_2751655,Human_miRNA_ID_2757788 RMVar_hsa_circ_42571,RMVar_hsa_circ_7895,RMVar_hsa_circ_116519,RMVar_hsa_circ_50487,RMVar_hsa_circ_344746,RMVar_hsa_circ_201987,RMVar_hsa_circ_367825 16020 RMVar_ID_16020 Human_SNP_ID_83774339 A-to-I Human chr2 + 97664836 97664836 97664836 AGCTTAAGCGATCCTCCCGCTTAGTCTTTCCAAAGCGTTGGGATTACAGGCGTCAGCTATTGCGC AGCTTAAGCGATCCTCCCGCTTAGTCTTTCCAGAGCGTTGGGATTACAGGCGTCAGCTATTGCGC A G C2orf92 Ensembl:ENSG00000228486 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs758134802 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13994008 16021 RMVar_ID_16021 Human_SNP_ID_83801355 A-to-I Human chr2 - 97773741 97773741 97773741 AGAATTAGCTGGGTGTGGTGGCATGTGCCTGTAGTCCTAGCTACTCAGGAGGCTGAGGTGAGAGG AGAATTAGCTGGGTGTGGTGGCATGTGCCTGTGGTCCTAGCTACTCAGGAGGCTGAGGTGAGAGG T C TMEM131 Ensembl:ENSG00000075568 Protein coding intron GSE47997;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 K562 cells&HepG2 cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 23474544,29129909,31158229 RNA-Seq:(High) rs1213547350 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110985,RMVar_hsa_circ_201991,RMVar_hsa_circ_4826,RMVar_hsa_circ_28003,RMVar_hsa_circ_74875,RMVar_hsa_circ_341806,RMVar_hsa_circ_25623,RMVar_hsa_circ_201993,RMVar_hsa_circ_12613,RMVar_hsa_circ_341607 16022 RMVar_ID_16022 Human_SNP_ID_83966179 A-to-I Human chr2 + 98457850 98457850 98457850 TAGAGACGGGGTCTCGCTCTGTTGCCCAGGCTATAGTGTAGTAGACAGCCATAGCTCGCTGCAGC TAGAGACGGGGTCTCGCTCTGTTGCCCAGGCTGTAGTGTAGTAGACAGCCATAGCTCGCTGCAGC A G INPP4A Ensembl:ENSG00000040933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs533684843 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6046 16023 RMVar_ID_16023 Human_SNP_ID_83975519 A-to-I Human chr2 + 98496637 98496637 98496637 TTTGCAAACTATACATTAGACAAGGGGTTAACATCAGAAACATACAAGGAACTCAAACAACTCAA TTTGCAAACTATACATTAGACAAGGGGTTAACGTCAGAAACATACAAGGAACTCAAACAACTCAA A G INPP4A Ensembl:ENSG00000040933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs576165251 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6046 16024 RMVar_ID_16024 Human_SNP_ID_83975521 A-to-I Human chr2 + 98496650 98496650 98496650 CATTAGACAAGGGGTTAACATCAGAAACATACAAGGAACTCAAACAACTCAATTGCAGGAAACAA CATTAGACAAGGGGTTAACATCAGAAACATACCAGGAACTCAAACAACTCAATTGCAGGAAACAA A C INPP4A Ensembl:ENSG00000040933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs541896649 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6046 16025 RMVar_ID_16025 Human_SNP_ID_83975769 A-to-I Human chr2 + 98497634 98497634 98497634 TTTTCTGCAGTTGAGTTGTTTGAGTTCCTTGTATGTTTCTGACGTTAACCCCTTGTCTAATATGT TTTTCTGCAGTTGAGTTGTTTGAGTTCCTTGTGTGTTTCTGACGTTAACCCCTTGTCTAATATGT A G INPP4A Ensembl:ENSG00000040933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1055425062 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6046 16026 RMVar_ID_16026 Human_SNP_ID_83986209 A-to-I Human chr2 + 98541605 98541604 98541606 AAGAGTTTATTCATTTTTTGTTAGCTTGAGACAGGGTATTGCTCTGTCACCCAGGCTGGAGTGCA AAGAGTTTATTCATTTTTTGTTAGCTTGAGAC__GGTATTGCTCTGTCACCCAGGCTGGAGTGCA CAG C INPP4A Ensembl:ENSG00000040933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1397646367 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_9291,RMVar_hsa_circ_9038,RMVar_hsa_circ_18622,RMVar_hsa_circ_340547,RMVar_hsa_circ_21658,RMVar_hsa_circ_107765,RMVar_hsa_circ_202032,RMVar_hsa_circ_55707,RMVar_hsa_circ_23808,RMVar_hsa_circ_202037,RMVar_hsa_circ_28183,RMVar_hsa_circ_2643,RMVar_hsa_circ_108799,RMVar_hsa_circ_75488,RMVar_hsa_circ_359690,RMVar_hsa_circ_93337,RMVar_hsa_circ_202040,RMVar_hsa_circ_318469,RMVar_hsa_circ_202041 16027 RMVar_ID_16027 Human_SNP_ID_83997965 A-to-I Human chr2 + 98590093 98590093 98590093 CTGTTTTATATATTCTTAGGTCATTCAAAGCCATGTATGCTGTAAATGTGCTAGTCTTTAGAATG CTGTTTTATATATTCTTAGGTCATTCAAAGCCGTGTATGCTGTAAATGTGCTAGTCTTTAGAATG A G INPP4A Ensembl:ENSG00000040933 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs575442921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_558514,Human_RBP_ID_1592061,Human_RBP_ID_1925659,Human_RBP_ID_3637449,Human_RBP_ID_8527830,Human_RBP_ID_21893750,Human_RBP_ID_23891017 Human_miRNA_ID_258229,Human_miRNA_ID_262024 16028 RMVar_ID_16028 Human_SNP_ID_84006405 A-to-I Human chr2 - 98622910 98622910 98622910 GCCTCAAGCAATCCTCCTGCCTCAGCCTCCCAAAGTGCTGGGATTATAGGTGTGTGCCACCATGT GCCTCAAGCAATCCTCCTGCCTCAGCCTCCCAGAGTGCTGGGATTATAGGTGTGTGCCACCATGT T C MGAT4A Ensembl:ENSG00000071073 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs936872270 Functional Loss SNV dbSNP153 33..33 33 - - - 16029 RMVar_ID_16029 Human_SNP_ID_84051864 A-to-I Human chr2 - 98812979 98812979 98812979 GTCATGGACTTAAATGTAAAATGAAAACTATAAAACTTTTAGAAAAAAATATGAGAAAATATTTG GTCATGGACTTAAATGTAAAATGAAAACTATACAACTTTTAGAAAAAAATATGAGAAAATATTTG T G KIAA1211L Ensembl:ENSG00000196872 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs897845076 Functional Loss SNV dbSNP153 33..33 33 - - - 16030 RMVar_ID_16030 Human_SNP_ID_84051869 A-to-I Human chr2 - 98812999 98812999 98812999 ACAAAATTAACTCAAAAGGGGTCATGGACTTAAATGTAAAATGAAAACTATAAAACTTTTAGAAA ACAAAATTAACTCAAAAGGGGTCATGGACTTACATGTAAAATGAAAACTATAAAACTTTTAGAAA T G KIAA1211L Ensembl:ENSG00000196872 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs954327662 Functional Loss SNV dbSNP153 33..33 33 - - - 16031 RMVar_ID_16031 Human_SNP_ID_84051873 A-to-I Human chr2 - 98813035 98813035 98813035 AAAAGTATGAACCTTGACCTAAGTCTTACATCATATACAAAATTAACTCAAAAGGGGTCATGGAC AAAAGTATGAACCTTGACCTAAGTCTTACATCGTATACAAAATTAACTCAAAAGGGGTCATGGAC T C KIAA1211L Ensembl:ENSG00000196872 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs758198014 Functional Loss SNV dbSNP153 33..33 33 - - - 16032 RMVar_ID_16032 Human_SNP_ID_84130465 A-to-I Human chr2 - 99145451 99145451 99145451 TGGGTTCAAGTGATTCTCGTGCCTCAGCTCCCAAGTAGCTGGGATTACAGGTGCCTGCCACCACG TGGGTTCAAGTGATTCTCGTGCCTCAGCTCCCGAGTAGCTGGGATTACAGGTGCCTGCCACCACG T C TSGA10 Ensembl:ENSG00000135951 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956641130 Functional Loss SNV dbSNP153 33..33 33 - - - 16033 RMVar_ID_16033 Human_SNP_ID_84133619 A-to-I Human chr2 + 99158338 99158338 99158338 CTGAAGTATAAATCCAAAGCCTTCATGCCTGTAATCCGAGTGCTTTAGGAGGCCAAGGCAGGAGG CTGAAGTATAAATCCAAAGCCTTCATGCCTGTGATCCGAGTGCTTTAGGAGGCCAAGGCAGGAGG A G AC092587.1,AC079447.1,LIPT1 Ensembl:ENSG00000273155,Ensembl:ENSG00000241962,Ensembl:ENSG00000144182 Protein coding,Protein coding,Protein coding intron,intron,intron GSE47997;GSE100210;GSE100210 K562 cells&HepG2 cells;HepG2 cell line;HepG2 cell line - 23474544,29129909,29129909 RNA-Seq:(High) rs981872434 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 16034 RMVar_ID_16034 Human_SNP_ID_84140755 A-to-I Human chr2 + 99186394 99186394 99186394 TCTCTCTGTCACCCAGGCTGGAGTGCAGTGGCACAATCTGGGCTCACTGTAGTCTCTGCCTCCCT TCTCTCTGTCACCCAGGCTGGAGTGCAGTGGCGCAATCTGGGCTCACTGTAGTCTCTGCCTCCCT A G AC092587.1,AC079447.1,MRPL30 Ensembl:ENSG00000273155,Ensembl:ENSG00000241962,Ensembl:ENSG00000185414 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1253797927 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_34624,RMVar_hsa_circ_202082,RMVar_hsa_circ_202083,RMVar_hsa_circ_202088,RMVar_hsa_circ_92876,RMVar_hsa_circ_271537,RMVar_hsa_circ_293193,RMVar_hsa_circ_338085,RMVar_hsa_circ_281092,RMVar_hsa_circ_95760,RMVar_hsa_circ_202093,RMVar_hsa_circ_202095,RMVar_hsa_circ_202096,RMVar_hsa_circ_202094,RMVar_hsa_circ_202092 16035 RMVar_ID_16035 Human_SNP_ID_84141662 A-to-I Human chr2 + 99190378 99190378 99190378 GTCCAGGAATTCAAGACCAGCCTGGGCAACATAGTGAGACTCTGTATCTACAAAAAATTTAAAAA GTCCAGGAATTCAAGACCAGCCTGGGCAACATGGTGAGACTCTGTATCTACAAAAAATTTAAAAA A G AC092587.1,AC079447.1,MRPL30 Ensembl:ENSG00000273155,Ensembl:ENSG00000241962,Ensembl:ENSG00000185414 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005152529 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96981,RMVar_hsa_circ_202081,RMVar_hsa_circ_81869,RMVar_hsa_circ_34624,RMVar_hsa_circ_202082,RMVar_hsa_circ_92876,RMVar_hsa_circ_293193,RMVar_hsa_circ_338085,RMVar_hsa_circ_281092,RMVar_hsa_circ_95760,RMVar_hsa_circ_202093,RMVar_hsa_circ_202095,RMVar_hsa_circ_202094,RMVar_hsa_circ_202092,RMVar_hsa_circ_202098,RMVar_hsa_circ_322564 16036 RMVar_ID_16036 Human_SNP_ID_84143130 A-to-I Human chr2 + 99195848 99195848 99195848 GCTCACCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGCAGATCACCTGAGGTCAAGAGTTCG GCTCACCTGTAATCCCAGCACTTTGGGAGGCCCAGGCGGGCAGATCACCTGAGGTCAAGAGTTCG A C AC079447.1,MRPL30 Ensembl:ENSG00000241962,Ensembl:ENSG00000185414 Protein coding,Protein coding intron,3'UTR GSE38233;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;esophageal squamous carcinoma cells,EC109 cell line - 24183664,32596459 RNA-Seq:(High) rs1052031841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24422337 RMVar_hsa_circ_96981,RMVar_hsa_circ_202081,RMVar_hsa_circ_81869,RMVar_hsa_circ_34624,RMVar_hsa_circ_202082,RMVar_hsa_circ_92876,RMVar_hsa_circ_281092,RMVar_hsa_circ_202093,RMVar_hsa_circ_202092,RMVar_hsa_circ_12561,RMVar_hsa_circ_298583,RMVar_hsa_circ_202101,RMVar_hsa_circ_202105,RMVar_hsa_circ_102414,RMVar_hsa_circ_274672,RMVar_hsa_circ_202104 16037 RMVar_ID_16037 Human_SNP_ID_84143131 A-to-I Human chr2 + 99195848 99195848 99195848 GCTCACCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGCAGATCACCTGAGGTCAAGAGTTCG GCTCACCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCAGATCACCTGAGGTCAAGAGTTCG A G AC079447.1,MRPL30 Ensembl:ENSG00000241962,Ensembl:ENSG00000185414 Protein coding,Protein coding intron,3'UTR GSE38233;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;esophageal squamous carcinoma cells,EC109 cell line - 24183664,32596459 RNA-Seq:(High) rs1052031841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24422337 RMVar_hsa_circ_96981,RMVar_hsa_circ_202081,RMVar_hsa_circ_81869,RMVar_hsa_circ_34624,RMVar_hsa_circ_202082,RMVar_hsa_circ_92876,RMVar_hsa_circ_281092,RMVar_hsa_circ_202093,RMVar_hsa_circ_202092,RMVar_hsa_circ_12561,RMVar_hsa_circ_298583,RMVar_hsa_circ_202101,RMVar_hsa_circ_202105,RMVar_hsa_circ_102414,RMVar_hsa_circ_274672,RMVar_hsa_circ_202104 16038 RMVar_ID_16038 Human_SNP_ID_84143161 A-to-I Human chr2 + 99195970 99195970 99195970 CAGGCATGGTGGCACATGCCTGTAACCCAGCTACTCGGGAGGCTGAAGCAGGAGAATCACTTGAA CAGGCATGGTGGCACATGCCTGTAACCCAGCTGCTCGGGAGGCTGAAGCAGGAGAATCACTTGAA A G AC079447.1,MRPL30 Ensembl:ENSG00000241962,Ensembl:ENSG00000185414 Protein coding,Protein coding intron,3'UTR GSE107867;GSE123020:GSM3490829,GSM3490830,GSM3490831 ASD brains,temporal_cortex;esophageal squamous carcinoma cells,EC109 cell line - 30559470,32596459 RNA-Seq:(High) rs1326258216 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_280151 RMVar_hsa_circ_96981,RMVar_hsa_circ_202081,RMVar_hsa_circ_81869,RMVar_hsa_circ_34624,RMVar_hsa_circ_202082,RMVar_hsa_circ_92876,RMVar_hsa_circ_281092,RMVar_hsa_circ_202093,RMVar_hsa_circ_202092,RMVar_hsa_circ_12561,RMVar_hsa_circ_298583,RMVar_hsa_circ_202101,RMVar_hsa_circ_202105,RMVar_hsa_circ_102414,RMVar_hsa_circ_274672,RMVar_hsa_circ_202104 16039 RMVar_ID_16039 Human_SNP_ID_84143165 A-to-I Human chr2 + 99195992 99195992 99195992 TAACCCAGCTACTCGGGAGGCTGAAGCAGGAGAATCACTTGAACCCGGGAGGCAGAGGTTGCAGT TAACCCAGCTACTCGGGAGGCTGAAGCAGGAGGATCACTTGAACCCGGGAGGCAGAGGTTGCAGT A G AC079447.1,MRPL30 Ensembl:ENSG00000241962,Ensembl:ENSG00000185414 Protein coding,Protein coding intron,3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1485126388 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_280151 RMVar_hsa_circ_96981,RMVar_hsa_circ_202081,RMVar_hsa_circ_81869,RMVar_hsa_circ_34624,RMVar_hsa_circ_202082,RMVar_hsa_circ_92876,RMVar_hsa_circ_281092,RMVar_hsa_circ_202093,RMVar_hsa_circ_202092,RMVar_hsa_circ_12561,RMVar_hsa_circ_298583,RMVar_hsa_circ_202101,RMVar_hsa_circ_202105,RMVar_hsa_circ_102414,RMVar_hsa_circ_274672,RMVar_hsa_circ_202104 16040 RMVar_ID_16040 Human_SNP_ID_84143263 A-to-I Human chr2 + 99196418 99196406 99196419 GACCTCCCAGGCTCAAGTGATCCTCCCACCTCAGCCTCCAGAGTAGCTAGGACTACAGGCAGTGT GACCTCCCAGGCTCAAGTGAT_____________CCTCCAGAGTAGCTAGGACTACAGGCAGTGT TCCTCCCACCTCAG T AC079447.1,MRPL30 Ensembl:ENSG00000241962,Ensembl:ENSG00000185414 Protein coding,Protein coding intron,3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1488735057 Functional Loss DEL dbSNP153 22..34 33 - - - Human_RBP_ID_25574084 Human_Splice_Rec_280152 RMVar_hsa_circ_96981,RMVar_hsa_circ_202081,RMVar_hsa_circ_81869,RMVar_hsa_circ_34624,RMVar_hsa_circ_202082,RMVar_hsa_circ_92876,RMVar_hsa_circ_281092,RMVar_hsa_circ_202093,RMVar_hsa_circ_202092,RMVar_hsa_circ_12561,RMVar_hsa_circ_298583,RMVar_hsa_circ_202101,RMVar_hsa_circ_202105,RMVar_hsa_circ_102414,RMVar_hsa_circ_274672,RMVar_hsa_circ_202104 16041 RMVar_ID_16041 Human_SNP_ID_84143266 A-to-I Human chr2 + 99196413 99196413 99196413 GCCTCGACCTCCCAGGCTCAAGTGATCCTCCCACCTCAGCCTCCAGAGTAGCTAGGACTACAGGC GCCTCGACCTCCCAGGCTCAAGTGATCCTCCCCCCTCAGCCTCCAGAGTAGCTAGGACTACAGGC A C AC079447.1,MRPL30 Ensembl:ENSG00000241962,Ensembl:ENSG00000185414 Protein coding,Protein coding intron,3'UTR GSE38233;GSE99789;GSE107867;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,EC109;ASD brains,temporal_cortex;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29796672,30559470,32596459,32596459 RNA-Seq:(High) rs563504306 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_280152 RMVar_hsa_circ_96981,RMVar_hsa_circ_202081,RMVar_hsa_circ_81869,RMVar_hsa_circ_34624,RMVar_hsa_circ_202082,RMVar_hsa_circ_92876,RMVar_hsa_circ_281092,RMVar_hsa_circ_202093,RMVar_hsa_circ_202092,RMVar_hsa_circ_12561,RMVar_hsa_circ_298583,RMVar_hsa_circ_202101,RMVar_hsa_circ_202105,RMVar_hsa_circ_102414,RMVar_hsa_circ_274672,RMVar_hsa_circ_202104 16042 RMVar_ID_16042 Human_SNP_ID_84143269 A-to-I Human chr2 + 99196418 99196418 99196418 GACCTCCCAGGCTCAAGTGATCCTCCCACCTCAGCCTCCAGAGTAGCTAGGACTACAGGCAGTGT GACCTCCCAGGCTCAAGTGATCCTCCCACCTCGGCCTCCAGAGTAGCTAGGACTACAGGCAGTGT A G AC079447.1,MRPL30 Ensembl:ENSG00000241962,Ensembl:ENSG00000185414 Protein coding,Protein coding intron,3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1214529219 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25574084 Human_Splice_Rec_280152 RMVar_hsa_circ_96981,RMVar_hsa_circ_202081,RMVar_hsa_circ_81869,RMVar_hsa_circ_34624,RMVar_hsa_circ_202082,RMVar_hsa_circ_92876,RMVar_hsa_circ_281092,RMVar_hsa_circ_202093,RMVar_hsa_circ_202092,RMVar_hsa_circ_12561,RMVar_hsa_circ_298583,RMVar_hsa_circ_202101,RMVar_hsa_circ_202105,RMVar_hsa_circ_102414,RMVar_hsa_circ_274672,RMVar_hsa_circ_202104 16043 RMVar_ID_16043 Human_SNP_ID_84143277 A-to-I Human chr2 + 99196440 99196440 99196440 CTCCCACCTCAGCCTCCAGAGTAGCTAGGACTACAGGCAGTGTGCCACCACATCCAGCTAATTTT CTCCCACCTCAGCCTCCAGAGTAGCTAGGACTGCAGGCAGTGTGCCACCACATCCAGCTAATTTT A G AC079447.1,MRPL30 Ensembl:ENSG00000241962,Ensembl:ENSG00000185414 Protein coding,Protein coding intron,3'UTR GSE38233;GSE100210;GSE99789;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,29796672,32596459 RNA-Seq:(High) rs1460581454 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6961211,Human_RBP_ID_17963736,Human_RBP_ID_26486147 Human_Splice_Rec_280152 RMVar_hsa_circ_96981,RMVar_hsa_circ_202081,RMVar_hsa_circ_81869,RMVar_hsa_circ_34624,RMVar_hsa_circ_202082,RMVar_hsa_circ_92876,RMVar_hsa_circ_281092,RMVar_hsa_circ_202093,RMVar_hsa_circ_202092,RMVar_hsa_circ_12561,RMVar_hsa_circ_298583,RMVar_hsa_circ_202101,RMVar_hsa_circ_202105,RMVar_hsa_circ_102414,RMVar_hsa_circ_274672,RMVar_hsa_circ_202104 16044 RMVar_ID_16044 Human_SNP_ID_84143287 A-to-I Human chr2 + 99196494 99196494 99196494 CAGCTAATTTTTTAAAGTTTTTTCATAGAGACAGGGACTCACTATGTTGTCCAAGCTGGTCTCAA CAGCTAATTTTTTAAAGTTTTTTCATAGAGACGGGGACTCACTATGTTGTCCAAGCTGGTCTCAA A G AC079447.1,MRPL30 Ensembl:ENSG00000241962,Ensembl:ENSG00000185414 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167182167 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6961212,Human_RBP_ID_13998305,Human_RBP_ID_17963737,Human_RBP_ID_18320147,Human_RBP_ID_26486150 RMVar_hsa_circ_96981,RMVar_hsa_circ_202081,RMVar_hsa_circ_81869,RMVar_hsa_circ_34624,RMVar_hsa_circ_202082,RMVar_hsa_circ_92876,RMVar_hsa_circ_281092,RMVar_hsa_circ_202093,RMVar_hsa_circ_202092,RMVar_hsa_circ_12561,RMVar_hsa_circ_298583,RMVar_hsa_circ_202101,RMVar_hsa_circ_202105,RMVar_hsa_circ_102414,RMVar_hsa_circ_274672,RMVar_hsa_circ_202104 16045 RMVar_ID_16045 Human_SNP_ID_84143499 A-to-I Human chr2 + 99197718 99197718 99197718 CCTGGAGGGCAGTGGTGTGATCGTAGCTCACTATTACCTCCAACTCTTGGGCTCAAGTGATCCTC CCTGGAGGGCAGTGGTGTGATCGTAGCTCACTGTTACCTCCAACTCTTGGGCTCAAGTGATCCTC A G AC079447.1,MRPL30 Ensembl:ENSG00000241962,Ensembl:ENSG00000185414 Protein coding,Protein coding intron,3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1034102656 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17963748 RMVar_hsa_circ_96981,RMVar_hsa_circ_202081,RMVar_hsa_circ_81869,RMVar_hsa_circ_34624,RMVar_hsa_circ_202082,RMVar_hsa_circ_92876,RMVar_hsa_circ_281092,RMVar_hsa_circ_202093,RMVar_hsa_circ_202092,RMVar_hsa_circ_12561,RMVar_hsa_circ_298583,RMVar_hsa_circ_202101,RMVar_hsa_circ_202105,RMVar_hsa_circ_102414,RMVar_hsa_circ_274672,RMVar_hsa_circ_202104 16046 RMVar_ID_16046 Human_SNP_ID_84143503 A-to-I Human chr2 + 99197740 99197740 99197740 GTAGCTCACTATTACCTCCAACTCTTGGGCTCAAGTGATCCTCCCACCTCAGCCTCCTGAGCAGC GTAGCTCACTATTACCTCCAACTCTTGGGCTCGAGTGATCCTCCCACCTCAGCCTCCTGAGCAGC A G AC079447.1,MRPL30 Ensembl:ENSG00000241962,Ensembl:ENSG00000185414 Protein coding,Protein coding intron,3'UTR GSE38233;GSE99789 cultured B-cells;esophageal squamous carcinoma cells,EC109 - 24183664,29796672 RNA-Seq:(High) rs1223527260 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96981,RMVar_hsa_circ_202081,RMVar_hsa_circ_81869,RMVar_hsa_circ_34624,RMVar_hsa_circ_202082,RMVar_hsa_circ_92876,RMVar_hsa_circ_281092,RMVar_hsa_circ_202093,RMVar_hsa_circ_202092,RMVar_hsa_circ_12561,RMVar_hsa_circ_298583,RMVar_hsa_circ_202101,RMVar_hsa_circ_202105,RMVar_hsa_circ_102414,RMVar_hsa_circ_274672,RMVar_hsa_circ_202104 16047 RMVar_ID_16047 Human_SNP_ID_84143530 A-to-I Human chr2 + 99197844 99197844 99197844 TTTTAAAATTTTTTGTAGAGCCAAGTGTTGCTATGTTGTCCACACTGATCTGGAGCTTCTAATCT TTTTAAAATTTTTTGTAGAGCCAAGTGTTGCTGTGTTGTCCACACTGATCTGGAGCTTCTAATCT A G AC079447.1,MRPL30 Ensembl:ENSG00000241962,Ensembl:ENSG00000185414 Protein coding,Protein coding intron,3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs913920317 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13998363 RMVar_hsa_circ_96981,RMVar_hsa_circ_202081,RMVar_hsa_circ_81869,RMVar_hsa_circ_34624,RMVar_hsa_circ_202082,RMVar_hsa_circ_92876,RMVar_hsa_circ_281092,RMVar_hsa_circ_202093,RMVar_hsa_circ_202092,RMVar_hsa_circ_12561,RMVar_hsa_circ_298583,RMVar_hsa_circ_202101,RMVar_hsa_circ_202105,RMVar_hsa_circ_102414,RMVar_hsa_circ_274672,RMVar_hsa_circ_202104 16048 RMVar_ID_16048 Human_SNP_ID_84143540 A-to-I Human chr2 + 99197872 99197872 99197872 TGCTATGTTGTCCACACTGATCTGGAGCTTCTAATCTCAAATGATTCTCCTGCCTCAGCCTCCCA TGCTATGTTGTCCACACTGATCTGGAGCTTCTTATCTCAAATGATTCTCCTGCCTCAGCCTCCCA A T AC079447.1,MRPL30 Ensembl:ENSG00000241962,Ensembl:ENSG00000185414 Protein coding,Protein coding intron,3'UTR GSE38233;GSE100210;GSE99789;GSE99789;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,29796672,29796672,32596459 RNA-Seq:(High) rs1046648604 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_558766,Human_RBP_ID_8527941,Human_RBP_ID_17963750 RMVar_hsa_circ_96981,RMVar_hsa_circ_202081,RMVar_hsa_circ_81869,RMVar_hsa_circ_34624,RMVar_hsa_circ_202082,RMVar_hsa_circ_92876,RMVar_hsa_circ_281092,RMVar_hsa_circ_202093,RMVar_hsa_circ_202092,RMVar_hsa_circ_12561,RMVar_hsa_circ_298583,RMVar_hsa_circ_202101,RMVar_hsa_circ_202105,RMVar_hsa_circ_102414,RMVar_hsa_circ_274672,RMVar_hsa_circ_202104 16049 RMVar_ID_16049 Human_SNP_ID_84144129 A-to-I Human chr2 + 99200531 99200531 99200531 AAACAAAAAATTTTAACTTAGCTGGGTGTGGTAGCACATGCCTGTAGTCCCAGCTGCTGAGGAGA AAACAAAAAATTTTAACTTAGCTGGGTGTGGTTGCACATGCCTGTAGTCCCAGCTGCTGAGGAGA A T AC079447.1 Ensembl:ENSG00000241962 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1192290027 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96981,RMVar_hsa_circ_202081,RMVar_hsa_circ_81869,RMVar_hsa_circ_34624,RMVar_hsa_circ_202082,RMVar_hsa_circ_92876,RMVar_hsa_circ_281092,RMVar_hsa_circ_202093,RMVar_hsa_circ_202092,RMVar_hsa_circ_12561,RMVar_hsa_circ_298583,RMVar_hsa_circ_202101,RMVar_hsa_circ_202105,RMVar_hsa_circ_102414,RMVar_hsa_circ_274672,RMVar_hsa_circ_202104 16050 RMVar_ID_16050 Human_SNP_ID_84144599 A-to-I Human chr2 + 99202800 99202799 99202800 GCCTGGGCAACATAGCAAGACCCCGTCTTTACAAAAAAAATTTTAAAAATGAGCTGGGTGAGGTG GCCTGGGCAACATAGCAAGACCCCGTCTTTAC_AAAAAAATTTTAAAAATGAGCTGGGTGAGGTG CA C AC079447.1 Ensembl:ENSG00000241962 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs147728655 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_22255284 RMVar_hsa_circ_96981,RMVar_hsa_circ_202081,RMVar_hsa_circ_81869,RMVar_hsa_circ_34624,RMVar_hsa_circ_202082,RMVar_hsa_circ_92876,RMVar_hsa_circ_281092,RMVar_hsa_circ_202093,RMVar_hsa_circ_202092,RMVar_hsa_circ_12561,RMVar_hsa_circ_298583,RMVar_hsa_circ_202101,RMVar_hsa_circ_202105,RMVar_hsa_circ_102414,RMVar_hsa_circ_274672,RMVar_hsa_circ_202104 16051 RMVar_ID_16051 Human_SNP_ID_84144600 A-to-I Human chr2 + 99202800 99202800 99202800 GCCTGGGCAACATAGCAAGACCCCGTCTTTACAAAAAAAATTTTAAAAATGAGCTGGGTGAGGTG GCCTGGGCAACATAGCAAGACCCCGTCTTTACTAAAAAAATTTTAAAAATGAGCTGGGTGAGGTG A T AC079447.1 Ensembl:ENSG00000241962 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1014367096 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22255284 RMVar_hsa_circ_96981,RMVar_hsa_circ_202081,RMVar_hsa_circ_81869,RMVar_hsa_circ_34624,RMVar_hsa_circ_202082,RMVar_hsa_circ_92876,RMVar_hsa_circ_281092,RMVar_hsa_circ_202093,RMVar_hsa_circ_202092,RMVar_hsa_circ_12561,RMVar_hsa_circ_298583,RMVar_hsa_circ_202101,RMVar_hsa_circ_202105,RMVar_hsa_circ_102414,RMVar_hsa_circ_274672,RMVar_hsa_circ_202104 16052 RMVar_ID_16052 Human_SNP_ID_84168209 A-to-I Human chr2 - 99306116 99306116 99306116 TTGGGAGGCTGAGGCCGGCGGATCATGAGGTCAGTAGATCGAGACCATCCTGGCTAACACGGTGA TTGGGAGGCTGAGGCCGGCGGATCATGAGGTCGGTAGATCGAGACCATCCTGGCTAACACGGTGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1262782696 Functional Loss SNV dbSNP153 33..33 33 - - - 16053 RMVar_ID_16053 Human_SNP_ID_84169734 A-to-I Human chr2 - 99312261 99312261 99312261 GAACTCCTGACCTCAAGTAACTCACTCACCTCAGCCTCCCAAAGTGCCAAGTGAAATATTTTAGT GAACTCCTGACCTCAAGTAACTCACTCACCTCGGCCTCCCAAAGTGCCAAGTGAAATATTTTAGT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs577846717 Functional Loss SNV dbSNP153 33..33 33 - - - 16054 RMVar_ID_16054 Human_SNP_ID_84169753 A-to-I Human chr2 - 99312339 99312339 99312339 GCATGTACCATCACGCCCAGCTAATTTTTCGTATTTTTAGTAGGGACGGGGTTTCACCATATTTG GCATGTACCATCACGCCCAGCTAATTTTTCGTGTTTTTAGTAGGGACGGGGTTTCACCATATTTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1465639268 Functional Loss SNV dbSNP153 33..33 33 - - - 16055 RMVar_ID_16055 Human_SNP_ID_84170048 A-to-I Human chr2 - 99313629 99313629 99313629 GATCTGCTGAGAGAAGATTTTTTTTAAGAGACAGGTCTTACTCTGTTGCCCAAGCTGGAGTGCAG GATCTGCTGAGAGAAGATTTTTTTTAAGAGACGGGTCTTACTCTGTTGCCCAAGCTGGAGTGCAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1019548080 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6961459 16056 RMVar_ID_16056 Human_SNP_ID_84171305 A-to-I Human chr2 - 99317953 99317953 99317953 GCGAGAGGCAGAGGTTGTAGTGGGCCAAGATCACACCACTCCACCCCAGCCTGGGTGACGGAGTG GCGAGAGGCAGAGGTTGTAGTGGGCCAAGATCCCACCACTCCACCCCAGCCTGGGTGACGGAGTG T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1380952694 Functional Loss SNV dbSNP153 33..33 33 - - - 16057 RMVar_ID_16057 Human_SNP_ID_84171311 A-to-I Human chr2 - 99317976 99317976 99317976 TGAGTCATGGGAATCGCTTGAACGCGAGAGGCAGAGGTTGTAGTGGGCCAAGATCACACCACTCC TGAGTCATGGGAATCGCTTGAACGCGAGAGGCGGAGGTTGTAGTGGGCCAAGATCACACCACTCC T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1192327036 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13999146 16058 RMVar_ID_16058 Human_SNP_ID_84171337 A-to-I Human chr2 - 99318055 99318055 99318055 GAAACCCTGTCTCTACTAAAAGTTTAAAAATTAGCCAGGCATCATGGCACGTGCCTGTAATTCCA GAAACCCTGTCTCTACTAAAAGTTTAAAAATTGGCCAGGCATCATGGCACGTGCCTGTAATTCCA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1260006850 Functional Loss SNV dbSNP153 33..33 33 - - - 16059 RMVar_ID_16059 Human_SNP_ID_84174781 A-to-I Human chr2 - 99332321 99332321 99332321 ATTCTGCCTCAGCCACCCGAGTAGCTGGGACTACAGGCGCACACCACCATGCCTGGCTAAGTTTT ATTCTGCCTCAGCCACCCGAGTAGCTGGGACTGCAGGCGCACACCACCATGCCTGGCTAAGTTTT T C TXNDC9 Ensembl:ENSG00000115514 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs560630002 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33871,RMVar_hsa_circ_125533,RMVar_hsa_circ_202111,RMVar_hsa_circ_23246 16060 RMVar_ID_16060 Human_SNP_ID_84174791 A-to-I Human chr2 - 99332360 99332360 99332360 CAACTCACTGCAACCTCCGCTTCCCGGCTTCAAGCAATTATTCTGCCTCAGCCACCCGAGTAGCT CAACTCACTGCAACCTCCGCTTCCCGGCTTCAGGCAATTATTCTGCCTCAGCCACCCGAGTAGCT T C TXNDC9 Ensembl:ENSG00000115514 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1163920216 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33871,RMVar_hsa_circ_125533,RMVar_hsa_circ_202111,RMVar_hsa_circ_23246 16061 RMVar_ID_16061 Human_SNP_ID_84175236 A-to-I Human chr2 - 99334229 99334229 99334229 CTCCCACTTCAGCCTCCCTAGTAGCGGGGACTACAGGCACACACCACCGGGCCTGGCCAATTTTT CTCCCACTTCAGCCTCCCTAGTAGCGGGGACTGCAGGCACACACCACCGGGCCTGGCCAATTTTT T C TXNDC9 Ensembl:ENSG00000115514 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1182116590 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125533,RMVar_hsa_circ_202111 16062 RMVar_ID_16062 Human_SNP_ID_84177586 A-to-I Human chr2 + 99342765 99342765 99342765 GCAGTCCTCCCTCCTCAGCCTCCCCAGTAGCTAGGACTGCAGGCATACACCACTGTACTCAGCTA GCAGTCCTCCCTCCTCAGCCTCCCCAGTAGCTGGGACTGCAGGCATACACCACTGTACTCAGCTA A G EIF5B Ensembl:ENSG00000158417 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs891856601 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13999552 16063 RMVar_ID_16063 Human_SNP_ID_84194007 A-to-I Human chr2 + 99407457 99407457 99407457 GCCTGTACCCCCAGCTACTCGGGAGGCTGAAGAAGGAGAATTGCTTGAACCCAGGAGGCGGAAGT GCCTGTACCCCCAGCTACTCGGGAGGCTGAAGCAGGAGAATTGCTTGAACCCAGGAGGCGGAAGT A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1237999737 Functional Loss SNV dbSNP153 33..33 33 - - - 16064 RMVar_ID_16064 Human_SNP_ID_84194525 A-to-I Human chr2 - 99409652 99409652 99409652 TTCAGTAGAGATAGGGTTTCACTATGTTGGCAAGGCTGATCTTGAACTCCTGACTTCAAATGATC TTCAGTAGAGATAGGGTTTCACTATGTTGGCAGGGCTGATCTTGAACTCCTGACTTCAAATGATC T C REV1 Ensembl:ENSG00000135945 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1236791406 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9540,RMVar_hsa_circ_65770,RMVar_hsa_circ_67414,RMVar_hsa_circ_28169,RMVar_hsa_circ_7261,RMVar_hsa_circ_53557,RMVar_hsa_circ_320753,RMVar_hsa_circ_66455,RMVar_hsa_circ_103196,RMVar_hsa_circ_52539,RMVar_hsa_circ_15795,RMVar_hsa_circ_9278,RMVar_hsa_circ_126522,RMVar_hsa_circ_202119,RMVar_hsa_circ_120537,RMVar_hsa_circ_202120,RMVar_hsa_circ_202121,RMVar_hsa_circ_322618,RMVar_hsa_circ_374675,RMVar_hsa_circ_41765,RMVar_hsa_circ_202122,RMVar_hsa_circ_12803 16065 RMVar_ID_16065 Human_SNP_ID_84194532 A-to-I Human chr2 - 99409672 99409672 99409672 GCCCAGCGAATTTTTGTATTTTCAGTAGAGATAGGGTTTCACTATGTTGGCAAGGCTGATCTTGA GCCCAGCGAATTTTTGTATTTTCAGTAGAGATGGGGTTTCACTATGTTGGCAAGGCTGATCTTGA T C REV1 Ensembl:ENSG00000135945 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs952286700 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9540,RMVar_hsa_circ_65770,RMVar_hsa_circ_67414,RMVar_hsa_circ_28169,RMVar_hsa_circ_7261,RMVar_hsa_circ_53557,RMVar_hsa_circ_320753,RMVar_hsa_circ_66455,RMVar_hsa_circ_103196,RMVar_hsa_circ_52539,RMVar_hsa_circ_15795,RMVar_hsa_circ_9278,RMVar_hsa_circ_126522,RMVar_hsa_circ_202119,RMVar_hsa_circ_120537,RMVar_hsa_circ_202120,RMVar_hsa_circ_202121,RMVar_hsa_circ_322618,RMVar_hsa_circ_374675,RMVar_hsa_circ_41765,RMVar_hsa_circ_202122,RMVar_hsa_circ_12803 16066 RMVar_ID_16066 Human_SNP_ID_84194557 A-to-I Human chr2 - 99409756 99409756 99409756 TCATTGCAACTTCTACCTCCTGGGTTCAAGCAATCCTCCTGTCTCAGCCTGTTGGGTAGCTGGGA TCATTGCAACTTCTACCTCCTGGGTTCAAGCAGTCCTCCTGTCTCAGCCTGTTGGGTAGCTGGGA T C REV1 Ensembl:ENSG00000135945 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs922307070 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9540,RMVar_hsa_circ_65770,RMVar_hsa_circ_67414,RMVar_hsa_circ_28169,RMVar_hsa_circ_7261,RMVar_hsa_circ_53557,RMVar_hsa_circ_320753,RMVar_hsa_circ_66455,RMVar_hsa_circ_103196,RMVar_hsa_circ_52539,RMVar_hsa_circ_15795,RMVar_hsa_circ_9278,RMVar_hsa_circ_126522,RMVar_hsa_circ_202119,RMVar_hsa_circ_120537,RMVar_hsa_circ_202120,RMVar_hsa_circ_202121,RMVar_hsa_circ_322618,RMVar_hsa_circ_374675,RMVar_hsa_circ_41765,RMVar_hsa_circ_202122,RMVar_hsa_circ_12803 16067 RMVar_ID_16067 Human_SNP_ID_84194761 A-to-I Human chr2 - 99410175 99410175 99410175 GAAACTCCATTTCCACTAAAAGTACAAAAATTAGCCGGACATGGTGGCATTCGCCTGTAGTCCCA GAAACTCCATTTCCACTAAAAGTACAAAAATTCGCCGGACATGGTGGCATTCGCCTGTAGTCCCA T G REV1 Ensembl:ENSG00000135945 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs71413837 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9540,RMVar_hsa_circ_65770,RMVar_hsa_circ_67414,RMVar_hsa_circ_28169,RMVar_hsa_circ_7261,RMVar_hsa_circ_53557,RMVar_hsa_circ_320753,RMVar_hsa_circ_66455,RMVar_hsa_circ_103196,RMVar_hsa_circ_52539,RMVar_hsa_circ_15795,RMVar_hsa_circ_9278,RMVar_hsa_circ_126522,RMVar_hsa_circ_202119,RMVar_hsa_circ_120537,RMVar_hsa_circ_202120,RMVar_hsa_circ_202121,RMVar_hsa_circ_322618,RMVar_hsa_circ_374675,RMVar_hsa_circ_41765,RMVar_hsa_circ_202122,RMVar_hsa_circ_12803 16068 RMVar_ID_16068 Human_SNP_ID_84195276 A-to-I Human chr2 - 99412066 99412066 99412066 ACCACGCCCGGCTAATTTTTTGTACTTTTAGTAGAGACGTGGTTTCACCGTGTTGGCCAGGCTGG ACCACGCCCGGCTAATTTTTTGTACTTTTAGTGGAGACGTGGTTTCACCGTGTTGGCCAGGCTGG T C REV1 Ensembl:ENSG00000135945 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs551415575 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9540,RMVar_hsa_circ_65770,RMVar_hsa_circ_28169,RMVar_hsa_circ_7261,RMVar_hsa_circ_53557,RMVar_hsa_circ_320753,RMVar_hsa_circ_66455,RMVar_hsa_circ_103196,RMVar_hsa_circ_52539,RMVar_hsa_circ_15795,RMVar_hsa_circ_9278,RMVar_hsa_circ_126522,RMVar_hsa_circ_202119,RMVar_hsa_circ_120537,RMVar_hsa_circ_202120,RMVar_hsa_circ_202121,RMVar_hsa_circ_322618,RMVar_hsa_circ_374675,RMVar_hsa_circ_41765,RMVar_hsa_circ_128091,RMVar_hsa_circ_202122,RMVar_hsa_circ_322111,RMVar_hsa_circ_351130,RMVar_hsa_circ_36779,RMVar_hsa_circ_202123,RMVar_hsa_circ_202124,RMVar_hsa_circ_202125 16069 RMVar_ID_16069 Human_SNP_ID_84206812 A-to-I Human chr2 - 99459019 99459019 99459019 TATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGTATGGTCTTGATCTCCTGACCTCGTGA TATTTTTAGTAGAGACGGGGTTTCACCGTGTTGGCCAGTATGGTCTTGATCTCCTGACCTCGTGA T C REV1 Ensembl:ENSG00000135945 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1311541314 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_143490 RMVar_hsa_circ_5764,RMVar_hsa_circ_65770,RMVar_hsa_circ_7261,RMVar_hsa_circ_103196,RMVar_hsa_circ_15795,RMVar_hsa_circ_9278,RMVar_hsa_circ_202119,RMVar_hsa_circ_120537,RMVar_hsa_circ_202120,RMVar_hsa_circ_374675,RMVar_hsa_circ_202122,RMVar_hsa_circ_351130,RMVar_hsa_circ_57150,RMVar_hsa_circ_202125,RMVar_hsa_circ_272611,RMVar_hsa_circ_202129,RMVar_hsa_circ_202130,RMVar_hsa_circ_376059,RMVar_hsa_circ_373667,RMVar_hsa_circ_202131,RMVar_hsa_circ_363408,RMVar_hsa_circ_202135,RMVar_hsa_circ_202136,RMVar_hsa_circ_350584,RMVar_hsa_circ_376037,RMVar_hsa_circ_202138,RMVar_hsa_circ_202137,RMVar_hsa_circ_292362,RMVar_hsa_circ_202140,RMVar_hsa_circ_94547,RMVar_hsa_circ_285563,RMVar_hsa_circ_202141,RMVar_hsa_circ_202142,RMVar_hsa_circ_271079,RMVar_hsa_circ_362656,RMVar_hsa_circ_202145,RMVar_hsa_circ_365803,RMVar_hsa_circ_322978,RMVar_hsa_circ_202147,RMVar_hsa_circ_202148,RMVar_hsa_circ_202149,RMVar_hsa_circ_289725,RMVar_hsa_circ_333944,RMVar_hsa_circ_202150 16070 RMVar_ID_16070 Human_SNP_ID_84208094 A-to-I Human chr2 - 99463897 99463897 99463897 CTCTGAGGTTGGGCGTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTCAGGCAGGTGG CTCTGAGGTTGGGCGTGGTGGCTCACACCTGTTATCCCAGCACTTTGGGAGGCTCAGGCAGGTGG T A REV1 Ensembl:ENSG00000135945 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs957187933 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_65770,RMVar_hsa_circ_7261,RMVar_hsa_circ_103196,RMVar_hsa_circ_9278,RMVar_hsa_circ_202119,RMVar_hsa_circ_374675,RMVar_hsa_circ_202122,RMVar_hsa_circ_351130,RMVar_hsa_circ_202125,RMVar_hsa_circ_272611,RMVar_hsa_circ_202129,RMVar_hsa_circ_202130,RMVar_hsa_circ_376059,RMVar_hsa_circ_373667,RMVar_hsa_circ_202131,RMVar_hsa_circ_202136,RMVar_hsa_circ_350584,RMVar_hsa_circ_202138,RMVar_hsa_circ_292362,RMVar_hsa_circ_202140,RMVar_hsa_circ_285563,RMVar_hsa_circ_202141,RMVar_hsa_circ_271079,RMVar_hsa_circ_202145,RMVar_hsa_circ_322978,RMVar_hsa_circ_202148,RMVar_hsa_circ_289725,RMVar_hsa_circ_202150,RMVar_hsa_circ_202151,RMVar_hsa_circ_275006 16071 RMVar_ID_16071 Human_SNP_ID_84209833 A-to-I Human chr2 - 99470564 99470564 99470564 CAGGCTATGACCTAACGCTTGCTTGGACCAGTATAAGCTTGCCGGGGCAAATATTTAGGCTAAAT CAGGCTATGACCTAACGCTTGCTTGGACCAGTGTAAGCTTGCCGGGGCAAATATTTAGGCTAAAT T C REV1 Ensembl:ENSG00000135945 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs552789172 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13556946 16072 RMVar_ID_16072 Human_SNP_ID_84209860 A-to-I Human chr2 - 99470674 99470674 99470674 TTAGCCAATCTTGTTTTAAAAGAGGCAAAGGCAGAGGAGAACAAAGGAAGGAGGAAGTAACTTGT TTAGCCAATCTTGTTTTAAAAGAGGCAAAGGCGGAGGAGAACAAAGGAAGGAGGAAGTAACTTGT T C REV1 Ensembl:ENSG00000135945 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs748332155 Functional Loss SNV dbSNP153 33..33 33 - - - 16073 RMVar_ID_16073 Human_SNP_ID_84401795 A-to-I Human chr2 - 100275580 100275580 100275580 ACCGGATTGAGGAATGAGTCACAACAGCTGCAAGGCTCTTAAAGCAACATTTAAACCTTTTGGCG ACCGGATTGAGGAATGAGTCACAACAGCTGCACGGCTCTTAAAGCAACATTTAAACCTTTTGGCG T G LONRF2 Ensembl:ENSG00000170500 Protein coding 3'UTR GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1255001850 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13558784 16074 RMVar_ID_16074 Human_SNP_ID_84585926 A-to-I Human chr2 + 101009216 101009216 101009216 GAGATTGAGACCATCCTGGCTAACACCTGGCTAACATGGTGAAACCCTGTCTCTATTAAAAATAC GAGATTGAGACCATCCTGGCTAACACCTGGCTGACATGGTGAAACCCTGTCTCTATTAAAAATAC A G RPL31 Ensembl:ENSG00000071082 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1275299129 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121270,RMVar_hsa_circ_202209 16075 RMVar_ID_16075 Human_SNP_ID_84595382 A-to-I Human chr2 - 101044859 101044858 101044860 CTGTAATCCCAGCTACTCAGGAGGCTGAGACAAGAGAATCCCATGAACCCAGGATGTGGAGCTTT CTGTAATCCCAGCTACTCAGGAGGCTGAGAC__GAGAATCCCATGAACCCAGGATGTGGAGCTTT CTT C TBC1D8 Ensembl:ENSG00000204634 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1483991957 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_104173,RMVar_hsa_circ_8248,RMVar_hsa_circ_354776,RMVar_hsa_circ_202217,RMVar_hsa_circ_69406,RMVar_hsa_circ_338520,RMVar_hsa_circ_329000,RMVar_hsa_circ_202221,RMVar_hsa_circ_367197,RMVar_hsa_circ_202222 16076 RMVar_ID_16076 Human_SNP_ID_84595383 A-to-I Human chr2 - 101044859 101044859 101044859 CTGTAATCCCAGCTACTCAGGAGGCTGAGACAAGAGAATCCCATGAACCCAGGATGTGGAGCTTT CTGTAATCCCAGCTACTCAGGAGGCTGAGACAGGAGAATCCCATGAACCCAGGATGTGGAGCTTT T C TBC1D8 Ensembl:ENSG00000204634 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1182822401 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104173,RMVar_hsa_circ_8248,RMVar_hsa_circ_354776,RMVar_hsa_circ_202217,RMVar_hsa_circ_69406,RMVar_hsa_circ_338520,RMVar_hsa_circ_329000,RMVar_hsa_circ_202221,RMVar_hsa_circ_367197,RMVar_hsa_circ_202222 16077 RMVar_ID_16077 Human_SNP_ID_84595625 A-to-I Human chr2 - 101045910 101045910 101045910 CAGCTCACTGTAGCCTCCACATCCTGGGTTCAAGAGATTCTCCTGCCTCAGCCTCCTGTGTAGCT CAGCTCACTGTAGCCTCCACATCCTGGGTTCAGGAGATTCTCCTGCCTCAGCCTCCTGTGTAGCT T C TBC1D8 Ensembl:ENSG00000204634 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs908311166 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104173,RMVar_hsa_circ_8248,RMVar_hsa_circ_354776,RMVar_hsa_circ_202217,RMVar_hsa_circ_69406,RMVar_hsa_circ_338520,RMVar_hsa_circ_329000,RMVar_hsa_circ_202221,RMVar_hsa_circ_367197,RMVar_hsa_circ_202222 16078 RMVar_ID_16078 Human_SNP_ID_84601514 A-to-I Human chr2 - 101070136 101070136 101070136 GAGGCGGGTAGATCACCTGAGGTCAGGAGTTCAAGACCAGCCTGACCAATGTGATGAAACCACAT GAGGCGGGTAGATCACCTGAGGTCAGGAGTTCCAGACCAGCCTGACCAATGTGATGAAACCACAT T G TBC1D8 Ensembl:ENSG00000204634 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs948777315 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3154,RMVar_hsa_circ_41759,RMVar_hsa_circ_331135,RMVar_hsa_circ_202228 16079 RMVar_ID_16079 Human_SNP_ID_84646747 A-to-I Human chr2 + 101257486 101257486 101257486 AGAACCTGAGAAGCACTCCTGGCCGATGTTTTAACTAAAGAAAACCTGTCTTTGACTGCCAGGCT AGAACCTGAGAAGCACTCCTGGCCGATGTTTTCACTAAAGAAAACCTGTCTTTGACTGCCAGGCT A C CNOT11 Ensembl:ENSG00000158435 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs531957380 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18397,RMVar_hsa_circ_202229,RMVar_hsa_circ_123572 16080 RMVar_ID_16080 Human_SNP_ID_84650114 A-to-I Human chr2 - 101271425 101271425 101271425 TTGCTATGTCCTCCAGTCTGGTCTTGAACTCAAGTGATCCACCCACCTTGGCCTCCCAAAGTGCT TTGCTATGTCCTCCAGTCTGGTCTTGAACTCAGGTGATCCACCCACCTTGGCCTCCCAAAGTGCT T C RNF149 Ensembl:ENSG00000163162 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202336294 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13560404,Human_RBP_ID_23815340 RMVar_hsa_circ_86551,RMVar_hsa_circ_116608,RMVar_hsa_circ_202245,RMVar_hsa_circ_202246 16081 RMVar_ID_16081 Human_SNP_ID_84650136 A-to-I Human chr2 - 101271520 101271520 101271520 TCAAGAAATCCTCCCACCTCAGCTTCCAGAGTAGCTGGGACTACAGGTGCATGCCACACCCTGAT TCAAGAAATCCTCCCACCTCAGCTTCCAGAGTTGCTGGGACTACAGGTGCATGCCACACCCTGAT T A RNF149 Ensembl:ENSG00000163162 Protein coding exon GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1231181708 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_530834 RMVar_hsa_circ_86551,RMVar_hsa_circ_116608,RMVar_hsa_circ_202245,RMVar_hsa_circ_202246 16082 RMVar_ID_16082 Human_SNP_ID_84650697 A-to-I Human chr2 - 101273611 101273611 101273611 AAAATTAGCCAGGTGTGGTGGCATCTGCCTGTAGTCCCAGCTGCTTGGGAAGCTGAGGTGGGAGG AAAATTAGCCAGGTGTGGTGGCATCTGCCTGTGGTCCCAGCTGCTTGGGAAGCTGAGGTGGGAGG T C RNF149 Ensembl:ENSG00000163162 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1320792635 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116608,RMVar_hsa_circ_202246 16083 RMVar_ID_16083 Human_SNP_ID_84651013 A-to-I Human chr2 - 101275067 101275067 101275067 GGAAGGGCCAGGCGTGGTGGCTCACGCCTCTAAACCCAGCACTTTGAGAGGCCAAGGTGGGAGGA GGAAGGGCCAGGCGTGGTGGCTCACGCCTCTATACCCAGCACTTTGAGAGGCCAAGGTGGGAGGA T A RNF149 Ensembl:ENSG00000163162 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs548829210 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116608,RMVar_hsa_circ_202246 16084 RMVar_ID_16084 Human_SNP_ID_84651882 A-to-I Human chr2 - 101278290 101278290 101278290 ATTAGCGGGGCGTGGTGGCGTGTGCCTACTGTAGTCCTAGCTCTCTGGGAAGCTGAGGTGGGAGG ATTAGCGGGGCGTGGTGGCGTGTGCCTACTGTCGTCCTAGCTCTCTGGGAAGCTGAGGTGGGAGG T G RNF149 Ensembl:ENSG00000163162 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1394839422 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25579396 RMVar_hsa_circ_116608,RMVar_hsa_circ_202246 16085 RMVar_ID_16085 Human_SNP_ID_84652249 A-to-I Human chr2 - 101280119 101280119 101280119 CAGTCTGGAGTGCAGTGACACGATCTCAGCTCACTGCAGCCTCTGCCTCCTGGGTTCAAGTGATT CAGTCTGGAGTGCAGTGACACGATCTCAGCTCCCTGCAGCCTCTGCCTCCTGGGTTCAAGTGATT T G RNF149 Ensembl:ENSG00000163162 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs906526106 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116608,RMVar_hsa_circ_202246 16086 RMVar_ID_16086 Human_SNP_ID_84653280 A-to-I Human chr2 - 101284425 101284425 101284425 ACCTGCACTCCAGTACACCCAGCTAATTTTTTATATTTTTTGTAGAGATAGGGTTTTACCACACT ACCTGCACTCCAGTACACCCAGCTAATTTTTTGTATTTTTTGTAGAGATAGGGTTTTACCACACT T C RNF149 Ensembl:ENSG00000163162 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1420238676 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116608,RMVar_hsa_circ_47063,RMVar_hsa_circ_202246,RMVar_hsa_circ_297721,RMVar_hsa_circ_309461,RMVar_hsa_circ_286206,RMVar_hsa_circ_202248,RMVar_hsa_circ_202249 16087 RMVar_ID_16087 Human_SNP_ID_84653918 A-to-I Human chr2 - 101287318 101287318 101287318 CTTAAGTACTGTTTTTTTTATTTTTTTGAGACAGAGTTTCGTTCTTGTTGCCCAGACTGGAGTAC CTTAAGTACTGTTTTTTTTATTTTTTTGAGACGGAGTTTCGTTCTTGTTGCCCAGACTGGAGTAC T C RNF149 Ensembl:ENSG00000163162 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1293649324 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2671068,Human_RBP_ID_13560866 RMVar_hsa_circ_116608,RMVar_hsa_circ_47063,RMVar_hsa_circ_202246,RMVar_hsa_circ_297721,RMVar_hsa_circ_286206,RMVar_hsa_circ_202248,RMVar_hsa_circ_202249,RMVar_hsa_circ_202250,RMVar_hsa_circ_311605,RMVar_hsa_circ_302862 16088 RMVar_ID_16088 Human_SNP_ID_84657409 A-to-I Human chr2 - 101301585 101301585 101301585 TACTATCTTTGAGGTGGGACATCGTGATGCATACCTGTAATCCTAGCACTTTGGGAGGATGAGGC TACTATCTTTGAGGTGGGACATCGTGATGCATTCCTGTAATCCTAGCACTTTGGGAGGATGAGGC T A RNF149 Ensembl:ENSG00000163162 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1473291106 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116608,RMVar_hsa_circ_202246 16089 RMVar_ID_16089 Human_SNP_ID_84657709 A-to-I Human chr2 - 101302856 101302856 101302856 CCAACCTTAGCCTTCTGCGTAGCTGGGACTACAGGTGCATGCTGCCACACCTGGCTAATTTTTTA CCAACCTTAGCCTTCTGCGTAGCTGGGACTACCGGTGCATGCTGCCACACCTGGCTAATTTTTTA T G RNF149 Ensembl:ENSG00000163162 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1428151348 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116608,RMVar_hsa_circ_202246 16090 RMVar_ID_16090 Human_SNP_ID_84657714 A-to-I Human chr2 - 101302893 101302893 101302893 TCGCTGTAGCTTTGCCCTTTAGGGATCAAGCAATCCTCCAACCTTAGCCTTCTGCGTAGCTGGGA TCGCTGTAGCTTTGCCCTTTAGGGATCAAGCAGTCCTCCAACCTTAGCCTTCTGCGTAGCTGGGA T C RNF149 Ensembl:ENSG00000163162 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1383362789 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116608,RMVar_hsa_circ_202246 16091 RMVar_ID_16091 Human_SNP_ID_84657778 A-to-I Human chr2 - 101303192 101303192 101303192 AGAATAGTTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCCGAGATTGCACCACTGCACTACAGCT AGAATAGTTTGAACCTGGGAGGCAGAGGTTGCCGTGAGCCGAGATTGCACCACTGCACTACAGCT T G RNF149 Ensembl:ENSG00000163162 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1263155336 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116608,RMVar_hsa_circ_202246 16092 RMVar_ID_16092 Human_SNP_ID_84658773 A-to-I Human chr2 - 101307306 101307306 101307306 GTGGTGGCGCCCGCCCGTAGTCTCAGGCACTCAGGAGCTGAGATGGGAGAATCACTTGAGCCCAG GTGGTGGCGCCCGCCCGTAGTCTCAGGCACTCTGGAGCTGAGATGGGAGAATCACTTGAGCCCAG T A RNF149 Ensembl:ENSG00000163162 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs997697752 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569821 RMVar_hsa_circ_116608,RMVar_hsa_circ_202246 16093 RMVar_ID_16093 Human_SNP_ID_84658774 A-to-I Human chr2 - 101307306 101307306 101307306 GTGGTGGCGCCCGCCCGTAGTCTCAGGCACTCAGGAGCTGAGATGGGAGAATCACTTGAGCCCAG GTGGTGGCGCCCGCCCGTAGTCTCAGGCACTCGGGAGCTGAGATGGGAGAATCACTTGAGCCCAG T C RNF149 Ensembl:ENSG00000163162 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs997697752 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569821 RMVar_hsa_circ_116608,RMVar_hsa_circ_202246 16094 RMVar_ID_16094 Human_SNP_ID_84658797 A-to-I Human chr2 - 101307406 101307406 101307406 GGGAGGCCGAGGTGGGAGGATCGTTTGAGGCCAGGAGTGTGAGACCAGCCTGGCCAACATAGACC GGGAGGCCGAGGTGGGAGGATCGTTTGAGGCCGGGAGTGTGAGACCAGCCTGGCCAACATAGACC T C RNF149 Ensembl:ENSG00000163162 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956959817 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569822 RMVar_hsa_circ_116608,RMVar_hsa_circ_202246 16095 RMVar_ID_16095 Human_SNP_ID_84758489 A-to-I Human chr2 + 101704652 101704652 101704652 TGGAGTGCAGTGGTGTGATCTCGGCCCACTGCAAGCTCTGCCTCCCAGGTTCAAGCGACTCTCCT TGGAGTGCAGTGGTGTGATCTCGGCCCACTGCCAGCTCTGCCTCCCAGGTTCAAGCGACTCTCCT A C MAP4K4 Ensembl:ENSG00000071054 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909601049 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13472,RMVar_hsa_circ_27514,RMVar_hsa_circ_340358,RMVar_hsa_circ_22836,RMVar_hsa_circ_97038,RMVar_hsa_circ_12605,RMVar_hsa_circ_202260 16096 RMVar_ID_16096 Human_SNP_ID_84758522 A-to-I Human chr2 + 101704762 101704762 101704762 TTGTATTTTTAGTAGAGATGGGGTTTCACCATATTGGCCAGGCTGGTCTCGAACTCGAGTCAGGG TTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCGAGTCAGGG A G MAP4K4 Ensembl:ENSG00000071054 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1390953864 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13472,RMVar_hsa_circ_27514,RMVar_hsa_circ_340358,RMVar_hsa_circ_22836,RMVar_hsa_circ_97038,RMVar_hsa_circ_12605,RMVar_hsa_circ_202260 16097 RMVar_ID_16097 Human_SNP_ID_84762327 A-to-I Human chr2 + 101719734 101719734 101719734 GATTGTGAGAATAAGAGTTCAAAAAGGGGGCCAGGCGTGGTGGCTCACGCCTGTAATCCCAGTGC GATTGTGAGAATAAGAGTTCAAAAAGGGGGCCGGGCGTGGTGGCTCACGCCTGTAATCCCAGTGC A G MAP4K4 Ensembl:ENSG00000071054 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1310025617 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13472,RMVar_hsa_circ_27514,RMVar_hsa_circ_340358,RMVar_hsa_circ_22836,RMVar_hsa_circ_97038,RMVar_hsa_circ_12605,RMVar_hsa_circ_202260 16098 RMVar_ID_16098 Human_SNP_ID_84764269 A-to-I Human chr2 + 101727697 101727697 101727697 GAAACAGAAAGAAGGTGGTAATGGTCGGGCACAGTGGCTCATGCCTGTAATCCCAGCACACTGGG GAAACAGAAAGAAGGTGGTAATGGTCGGGCACGGTGGCTCATGCCTGTAATCCCAGCACACTGGG A G MAP4K4 Ensembl:ENSG00000071054 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1559115773 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13472,RMVar_hsa_circ_27514,RMVar_hsa_circ_340358,RMVar_hsa_circ_22836,RMVar_hsa_circ_97038,RMVar_hsa_circ_12605,RMVar_hsa_circ_202260 16099 RMVar_ID_16099 Human_SNP_ID_84794702 A-to-I Human chr2 + 101848067 101848067 101848067 GCAATAGGCTACACCATATGGCCTAGGTGTGTAATAGGCTGTACCATCTAGGTTTGTGTGTGCAC GCAATAGGCTACACCATATGGCCTAGGTGTGTTATAGGCTGTACCATCTAGGTTTGTGTGTGCAC A T MAP4K4 Ensembl:ENSG00000071054 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1341891505 Functional Loss SNV dbSNP153 33..33 33 - - - 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 16100 RMVar_ID_16100 Human_SNP_ID_84794719 A-to-I Human chr2 + 101848103 101848103 101848103 GGCTGTACCATCTAGGTTTGTGTGTGCACACTATATGATGTTCATACAATGAAGAAATCACCTAA GGCTGTACCATCTAGGTTTGTGTGTGCACACTGTATGATGTTCATACAATGAAGAAATCACCTAA A G MAP4K4 Ensembl:ENSG00000071054 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1396764050 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20440962 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 16101 RMVar_ID_16101 Human_SNP_ID_84794734 A-to-I Human chr2 + 101848154 101848154 101848154 AAGAAATCACCTAACGACGCATTTCTAGGAACATATCCCTGTTGTTAAGCAACACATGACTGTAC AAGAAATCACCTAACGACGCATTTCTAGGAACGTATCCCTGTTGTTAAGCAACACATGACTGTAC A G MAP4K4 Ensembl:ENSG00000071054 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank;ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs971342486 Functional Loss SNV dbSNP153 33..33 33 - - - 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 16102 RMVar_ID_16102 Human_SNP_ID_85015656 A-to-I Human chr2 - 102717168 102717168 102717168 AAAATTAGCCGGGCGTGATGGCGGGCGCCTGCAGTCCCAGCTATTCGGGAGGCTGAGGTAGAATG AAAATTAGCCGGGCGTGATGGCGGGCGCCTGCGGTCCCAGCTATTCGGGAGGCTGAGGTAGAATG T C MFSD9 Ensembl:ENSG00000135953 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs970158811 Functional Loss SNV dbSNP153 33..33 33 - - - 16103 RMVar_ID_16103 Human_SNP_ID_379922029 A-to-I Human chr8 + 120019144 120019144 120019144 CTGGCCAACATGGCGAAACCCCGTCTCTACTGAGAATACAAAAATTAGCCTGGCATGGTGGCCCA CTGGCCAACATGGCGAAACCCCGTCTCTACTGCGAATACAAAAATTAGCCTGGCATGGTGGCCCA A C DEPTOR Ensembl:ENSG00000155792 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1376233706 Functional Loss SNV dbSNP153 33..33 33 - - - 16104 RMVar_ID_16104 Human_SNP_ID_379930353 A-to-I Human chr8 + 120053844 120053844 120053844 CTCAAGGCAACTTCTACTTCCCAAGTTCAAGCAATTCTTCTGTTTGAGCCTCCTGAGTAGTGGGA CTCAAGGCAACTTCTACTTCCCAAGTTCAAGCGATTCTTCTGTTTGAGCCTCCTGAGTAGTGGGA A G AC091563.1 Ensembl:ENSG00000254343 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs763013524 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5251645 16105 RMVar_ID_16105 Human_SNP_ID_380024692 A-to-I Human chr8 + 120452664 120452664 120452664 CAGCCTGGCTAACATGGTGAAACCCCTTTTCTACTGAAAATAGAAAAAATTAGCCGGGCGTGGTG CAGCCTGGCTAACATGGTGAAACCCCTTTTCTGCTGAAAATAGAAAAAATTAGCCGGGCGTGGTG A G MTBP Ensembl:ENSG00000172167 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1460595009 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40722,RMVar_hsa_circ_38887 16106 RMVar_ID_16106 Human_SNP_ID_380027632 A-to-I Human chr8 + 120464953 120464953 120464953 CATTTTAGGGGACCAACAGAAAATAAATAACTACAGACATAATAAGAATTATGAAGAAATAAACA CATTTTAGGGGACCAACAGAAAATAAATAACTGCAGACATAATAAGAATTATGAAGAAATAAACA A G MTBP Ensembl:ENSG00000172167 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10102834 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38887,RMVar_hsa_circ_60310,RMVar_hsa_circ_254111,RMVar_hsa_circ_295640,RMVar_hsa_circ_332117,RMVar_hsa_circ_306000,RMVar_hsa_circ_55747,RMVar_hsa_circ_56910,RMVar_hsa_circ_254112,RMVar_hsa_circ_333596,RMVar_hsa_circ_347384,RMVar_hsa_circ_282170,RMVar_hsa_circ_254114,RMVar_hsa_circ_254113 16107 RMVar_ID_16107 Human_SNP_ID_380027976 A-to-I Human chr8 + 120466351 120466351 120466351 CTCCCGGCTCAGCCACTCAACTACCTAGAACTACAAGCATACACCACCATGGTTGGCTAATTTTT CTCCCGGCTCAGCCACTCAACTACCTAGAACTGCAAGCATACACCACCATGGTTGGCTAATTTTT A G MTBP Ensembl:ENSG00000172167 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1196040400 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16337437 RMVar_hsa_circ_38887,RMVar_hsa_circ_60310,RMVar_hsa_circ_254111,RMVar_hsa_circ_295640,RMVar_hsa_circ_332117,RMVar_hsa_circ_306000,RMVar_hsa_circ_55747,RMVar_hsa_circ_56910,RMVar_hsa_circ_254112,RMVar_hsa_circ_333596,RMVar_hsa_circ_347384,RMVar_hsa_circ_282170,RMVar_hsa_circ_254114,RMVar_hsa_circ_254113 16108 RMVar_ID_16108 Human_SNP_ID_380607512 A-to-I Human chr8 + 122827159 122827159 122827159 CTCCCACCTCAGCCACCCAAGTAGCTGTGACTACAAGTTTGCGCCACCATGCCTAGCTAATTTTG CTCCCACCTCAGCCACCCAAGTAGCTGTGACTGCAAGTTTGCGCCACCATGCCTAGCTAATTTTG A G ZHX2 Ensembl:ENSG00000178764 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs994857268 Functional Loss SNV dbSNP153 33..33 33 - - - 16109 RMVar_ID_16109 Human_SNP_ID_380642185 A-to-I Human chr8 + 122974387 122974387 122974387 TATGAACTCTGGTTGCAATCCCTCCCCGTCCCACACTGCCCCCCATTTGAGTACACCGCACAAGT TATGAACTCTGGTTGCAATCCCTCCCCGTCCCTCACTGCCCCCCATTTGAGTACACCGCACAAGT A T ZHX2 Ensembl:ENSG00000178764 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1203827290 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18961653 16110 RMVar_ID_16110 Human_SNP_ID_380662825 A-to-I Human chr8 + 123058174 123058174 123058174 TGTTTTATGAGAACACCTAAGCATGAATATTTATTAAAGCAGCTTGGAACACATCTCTTTGATTT TGTTTTATGAGAACACCTAAGCATGAATATTTGTTAAAGCAGCTTGGAACACATCTCTTTGATTT A G TBC1D31 Ensembl:ENSG00000156787 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1419222638 Functional Loss SNV dbSNP153 33..33 33 - - - 16111 RMVar_ID_16111 Human_SNP_ID_380666806 A-to-I Human chr8 + 123073784 123073784 123073784 CTCGGCTCACTGCATCCTCCACCTCCCGAGTTAAAGCGATTCTCTTGCCTCAGCCTCCTAAGTAG CTCGGCTCACTGCATCCTCCACCTCCCGAGTTCAAGCGATTCTCTTGCCTCAGCCTCCTAAGTAG A C TBC1D31 Ensembl:ENSG00000156787 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1351924820 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_254135,RMVar_hsa_circ_103459 16112 RMVar_ID_16112 Human_SNP_ID_380666941 A-to-I Human chr8 + 123074227 123074227 123074227 TTTTTGTATTTTTAGTAGAGACGGACCGTGTTAGCCAGGATGGTCTTGATCTCCTGATGTCGTGA TTTTTGTATTTTTAGTAGAGACGGACCGTGTTTGCCAGGATGGTCTTGATCTCCTGATGTCGTGA A T TBC1D31 Ensembl:ENSG00000156787 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs570724688 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16339114 RMVar_hsa_circ_254135,RMVar_hsa_circ_103459 16113 RMVar_ID_16113 Human_SNP_ID_380667782 A-to-I Human chr8 + 123077625 123077625 123077625 ATGATCTCAGCTTACTGCAAACTCCGCCTCCCAGGTTCCAGCTACCGCACCCAGCCCATAGTTGC ATGATCTCAGCTTACTGCAAACTCCGCCTCCCGGGTTCCAGCTACCGCACCCAGCCCATAGTTGC A G TBC1D31 Ensembl:ENSG00000156787 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1011134499 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_254146,RMVar_hsa_circ_292135,RMVar_hsa_circ_254135,RMVar_hsa_circ_103459,RMVar_hsa_circ_298814,RMVar_hsa_circ_318326,RMVar_hsa_circ_338515,RMVar_hsa_circ_347964,RMVar_hsa_circ_362056,RMVar_hsa_circ_318736,RMVar_hsa_circ_313147,RMVar_hsa_circ_317032,RMVar_hsa_circ_310280,RMVar_hsa_circ_297281,RMVar_hsa_circ_298414,RMVar_hsa_circ_294957,RMVar_hsa_circ_31481,RMVar_hsa_circ_275777,RMVar_hsa_circ_280243,RMVar_hsa_circ_271268,RMVar_hsa_circ_254148,RMVar_hsa_circ_254150,RMVar_hsa_circ_254152,RMVar_hsa_circ_254153,RMVar_hsa_circ_254151,RMVar_hsa_circ_254149,RMVar_hsa_circ_254147,RMVar_hsa_circ_254138,RMVar_hsa_circ_254142,RMVar_hsa_circ_254144,RMVar_hsa_circ_254145,RMVar_hsa_circ_254143,RMVar_hsa_circ_254140,RMVar_hsa_circ_254141,RMVar_hsa_circ_254139,RMVar_hsa_circ_254136,RMVar_hsa_circ_254137 16114 RMVar_ID_16114 Human_SNP_ID_380683860 A-to-I Human chr8 + 123148482 123148482 123148482 TCTCAGCTCTGGCTGGGCACGGTGGCGCCTGTAATCCTAGCAATTTGGGAGACTGAGGCGGGAGG TCTCAGCTCTGGCTGGGCACGGTGGCGCCTGTTATCCTAGCAATTTGGGAGACTGAGGCGGGAGG A T TBC1D31 Ensembl:ENSG00000156787 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1263284624 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_338515,RMVar_hsa_circ_254136,RMVar_hsa_circ_64145,RMVar_hsa_circ_31158 16115 RMVar_ID_16115 Human_SNP_ID_380703441 A-to-I Human chr8 - 123224420 123224420 123224420 TTTTGTAGAGGCAGGGTCTTGCTATGTTGCCCAGTCTGGTCCCAAACTCCTGGCCTCAAATGATC TTTTGTAGAGGCAGGGTCTTGCTATGTTGCCCGGTCTGGTCCCAAACTCCTGGCCTCAAATGATC T C C8orf76 Ensembl:ENSG00000189376 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs752019315 Functional Loss SNV dbSNP153 33..33 33 - - - 16116 RMVar_ID_16116 Human_SNP_ID_380703460 A-to-I Human chr8 - 123224496 123224496 123224496 GTGGTCCTTTCACCTCAGCCTCCCAAGTTCGTAGGATTACAGGCACCCACCACCATGTCCAGCTA GTGGTCCTTTCACCTCAGCCTCCCAAGTTCGTGGGATTACAGGCACCCACCACCATGTCCAGCTA T C C8orf76 Ensembl:ENSG00000189376 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1450398706 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16339664 16117 RMVar_ID_16117 Human_SNP_ID_380704484 A-to-I Human chr8 - 123228457 123228457 123228457 GCACCACCATGCCAGGCTAATTTTGTGTTTTTAGTAGAGATGGGATTTCTCCATGTTGGTCAGGC GCACCACCATGCCAGGCTAATTTTGTGTTTTTCGTAGAGATGGGATTTCTCCATGTTGGTCAGGC T G C8orf76,ZHX1-C8orf76 Ensembl:ENSG00000189376,Ensembl:ENSG00000259305 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1217770770 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105780,RMVar_hsa_circ_254175,RMVar_hsa_circ_254174,RMVar_hsa_circ_300129,RMVar_hsa_circ_308653 16118 RMVar_ID_16118 Human_SNP_ID_380705013 A-to-I Human chr8 - 123230727 123230727 123230727 GGGAATCGCTGAACCCGGGAGGCGGAGGTTGCAGTGAGCTGAGATCGTGCCACTGCACTCCAGCC GGGAATCGCTGAACCCGGGAGGCGGAGGTTGCGGTGAGCTGAGATCGTGCCACTGCACTCCAGCC T C C8orf76,ZHX1-C8orf76 Ensembl:ENSG00000189376,Ensembl:ENSG00000259305 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1385399514 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105780,RMVar_hsa_circ_254175,RMVar_hsa_circ_254174,RMVar_hsa_circ_300129,RMVar_hsa_circ_308653 16119 RMVar_ID_16119 Human_SNP_ID_380709434 A-to-I Human chr8 - 123247642 123247642 123247642 ATTATAAGCCCAGTGCGATGGTCTGTGTCTGTAGTCCCAGCTACCAGGGAGGCTGAGGTGGGAGG ATTATAAGCCCAGTGCGATGGTCTGTGTCTGTGGTCCCAGCTACCAGGGAGGCTGAGGTGGGAGG T C ZHX1-C8orf76 Ensembl:ENSG00000259305 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs925812159 Functional Loss SNV dbSNP153 33..33 33 - - - 16120 RMVar_ID_16120 Human_SNP_ID_380719041 A-to-I Human chr8 + 123289648 123289648 123289648 GCTGATGTCCTAGATAAAGGATCTGGTGTAGTAATTCTTATGGATGTCTATTCTTATTCTAAGAA GCTGATGTCCTAGATAAAGGATCTGGTGTAGTGATTCTTATGGATGTCTATTCTTATTCTAAGAA A G AC018992.1 Ensembl:ENSG00000253336 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1406476640 Functional Loss SNV dbSNP153 33..33 33 - - - 16121 RMVar_ID_16121 Human_SNP_ID_380719048 A-to-I Human chr8 + 123289676 123289676 123289676 TAGTAATTCTTATGGATGTCTATTCTTATTCTAAGAAGGAATTTATGTGCTATAATCAGTCCTCT TAGTAATTCTTATGGATGTCTATTCTTATTCTGAGAAGGAATTTATGTGCTATAATCAGTCCTCT A G AC018992.1 Ensembl:ENSG00000253336 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1182478443 Functional Loss SNV dbSNP153 33..33 33 - - - 16122 RMVar_ID_16122 Human_SNP_ID_380727036 A-to-I Human chr8 - 123322238 123322238 123322238 CATGCCTGTAATCCCAGCACTTGGGGAAGCCAAGGCGGGTGGATTGCTTGAGCCCAGGAGTTCAA CATGCCTGTAATCCCAGCACTTGGGGAAGCCAGGGCGGGTGGATTGCTTGAGCCCAGGAGTTCAA T C ATAD2 Ensembl:ENSG00000156802 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs982999209 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17578732 16123 RMVar_ID_16123 Human_SNP_ID_380727037 A-to-I Human chr8 - 123322243 123322243 123322243 TGGCTCATGCCTGTAATCCCAGCACTTGGGGAAGCCAAGGCGGGTGGATTGCTTGAGCCCAGGAG TGGCTCATGCCTGTAATCCCAGCACTTGGGGAGGCCAAGGCGGGTGGATTGCTTGAGCCCAGGAG T C ATAD2 Ensembl:ENSG00000156802 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs569665323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17578732 16124 RMVar_ID_16124 Human_SNP_ID_380728209 A-to-I Human chr8 - 123327040 123327040 123327040 GCTGGGCGTGGTGGCTAACGCCTGTAGTCCCAACTGCTCTGGAGGCTGAGGCAGGAGAATCACCT GCTGGGCGTGGTGGCTAACGCCTGTAGTCCCAGCTGCTCTGGAGGCTGAGGCAGGAGAATCACCT T C ATAD2 Ensembl:ENSG00000156802 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs966003972 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16340656 RMVar_hsa_circ_254182,RMVar_hsa_circ_104449,RMVar_hsa_circ_303709,RMVar_hsa_circ_312417,RMVar_hsa_circ_114558,RMVar_hsa_circ_44187,RMVar_hsa_circ_86390,RMVar_hsa_circ_254184,RMVar_hsa_circ_36233,RMVar_hsa_circ_254185,RMVar_hsa_circ_254183,RMVar_hsa_circ_254187,RMVar_hsa_circ_297248,RMVar_hsa_circ_254181,RMVar_hsa_circ_356102,RMVar_hsa_circ_294404,RMVar_hsa_circ_254186 16125 RMVar_ID_16125 Human_SNP_ID_380729264 A-to-I Human chr8 - 123331034 123331034 123331034 CCTGTAATCCCAGCCCTCAAGGGACTGAGGCAAGAGAATTGCTTGAACCCAGTGGGGCAGAGGTT CCTGTAATCCCAGCCCTCAAGGGACTGAGGCATGAGAATTGCTTGAACCCAGTGGGGCAGAGGTT T A ATAD2 Ensembl:ENSG00000156802 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025121050 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_254182,RMVar_hsa_circ_104449,RMVar_hsa_circ_312417,RMVar_hsa_circ_114558,RMVar_hsa_circ_44187,RMVar_hsa_circ_86390,RMVar_hsa_circ_254184,RMVar_hsa_circ_36233,RMVar_hsa_circ_254183,RMVar_hsa_circ_254187,RMVar_hsa_circ_297248,RMVar_hsa_circ_254181,RMVar_hsa_circ_356102,RMVar_hsa_circ_294404,RMVar_hsa_circ_92139,RMVar_hsa_circ_254186,RMVar_hsa_circ_352479,RMVar_hsa_circ_54919,RMVar_hsa_circ_254188 16126 RMVar_ID_16126 Human_SNP_ID_380729265 A-to-I Human chr8 - 123331034 123331034 123331034 CCTGTAATCCCAGCCCTCAAGGGACTGAGGCAAGAGAATTGCTTGAACCCAGTGGGGCAGAGGTT CCTGTAATCCCAGCCCTCAAGGGACTGAGGCAGGAGAATTGCTTGAACCCAGTGGGGCAGAGGTT T C ATAD2 Ensembl:ENSG00000156802 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025121050 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_254182,RMVar_hsa_circ_104449,RMVar_hsa_circ_312417,RMVar_hsa_circ_114558,RMVar_hsa_circ_44187,RMVar_hsa_circ_86390,RMVar_hsa_circ_254184,RMVar_hsa_circ_36233,RMVar_hsa_circ_254183,RMVar_hsa_circ_254187,RMVar_hsa_circ_297248,RMVar_hsa_circ_254181,RMVar_hsa_circ_356102,RMVar_hsa_circ_294404,RMVar_hsa_circ_92139,RMVar_hsa_circ_254186,RMVar_hsa_circ_352479,RMVar_hsa_circ_54919,RMVar_hsa_circ_254188 16127 RMVar_ID_16127 Human_SNP_ID_380729365 A-to-I Human chr8 - 123331439 123331439 123331439 GATCAAGAGTTTGAGACAAGCCTGGTCAACACAGTGAAACCCCGTCTCTACTAAAAATAAAAAAA GATCAAGAGTTTGAGACAAGCCTGGTCAACACCGTGAAACCCCGTCTCTACTAAAAATAAAAAAA T G ATAD2 Ensembl:ENSG00000156802 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs932216439 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_254182,RMVar_hsa_circ_104449,RMVar_hsa_circ_312417,RMVar_hsa_circ_114558,RMVar_hsa_circ_44187,RMVar_hsa_circ_86390,RMVar_hsa_circ_254184,RMVar_hsa_circ_36233,RMVar_hsa_circ_254183,RMVar_hsa_circ_254187,RMVar_hsa_circ_297248,RMVar_hsa_circ_254181,RMVar_hsa_circ_356102,RMVar_hsa_circ_294404,RMVar_hsa_circ_92139,RMVar_hsa_circ_254186,RMVar_hsa_circ_352479,RMVar_hsa_circ_54919,RMVar_hsa_circ_254188 16128 RMVar_ID_16128 Human_SNP_ID_380731749 A-to-I Human chr8 - 123341081 123341081 123341081 TGAATAAAATGAGCATGGTGGTGTGCACCTATAGTCCCAGCTACTCGGGAGGCTGAAGTGGGAGA TGAATAAAATGAGCATGGTGGTGTGCACCTATCGTCCCAGCTACTCGGGAGGCTGAAGTGGGAGA T G ATAD2 Ensembl:ENSG00000156802 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1305913588 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26150200 RMVar_hsa_circ_86390,RMVar_hsa_circ_36233,RMVar_hsa_circ_4007,RMVar_hsa_circ_254181,RMVar_hsa_circ_92139,RMVar_hsa_circ_54919,RMVar_hsa_circ_266235,RMVar_hsa_circ_254188,RMVar_hsa_circ_58502,RMVar_hsa_circ_115520,RMVar_hsa_circ_50757,RMVar_hsa_circ_18620,RMVar_hsa_circ_254192,RMVar_hsa_circ_69993,RMVar_hsa_circ_106044,RMVar_hsa_circ_52754,RMVar_hsa_circ_97981,RMVar_hsa_circ_254193,RMVar_hsa_circ_254195,RMVar_hsa_circ_45204,RMVar_hsa_circ_366710,RMVar_hsa_circ_338266 16129 RMVar_ID_16129 Human_SNP_ID_380731750 A-to-I Human chr8 - 123341083 123341083 123341083 AATGAATAAAATGAGCATGGTGGTGTGCACCTATAGTCCCAGCTACTCGGGAGGCTGAAGTGGGA AATGAATAAAATGAGCATGGTGGTGTGCACCTGTAGTCCCAGCTACTCGGGAGGCTGAAGTGGGA T C ATAD2 Ensembl:ENSG00000156802 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs557966279 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86390,RMVar_hsa_circ_36233,RMVar_hsa_circ_4007,RMVar_hsa_circ_254181,RMVar_hsa_circ_92139,RMVar_hsa_circ_54919,RMVar_hsa_circ_266235,RMVar_hsa_circ_254188,RMVar_hsa_circ_58502,RMVar_hsa_circ_115520,RMVar_hsa_circ_50757,RMVar_hsa_circ_18620,RMVar_hsa_circ_254192,RMVar_hsa_circ_69993,RMVar_hsa_circ_106044,RMVar_hsa_circ_52754,RMVar_hsa_circ_97981,RMVar_hsa_circ_254193,RMVar_hsa_circ_254195,RMVar_hsa_circ_45204,RMVar_hsa_circ_366710,RMVar_hsa_circ_338266 16130 RMVar_ID_16130 Human_SNP_ID_380735064 A-to-I Human chr8 - 123354088 123354088 123354088 GCTCTGTCGCCCAGGCTGGAGTGCAGTAGCACAGTCTTGGCTCACTGCAACCTCTGCCTCCCGAG GCTCTGTCGCCCAGGCTGGAGTGCAGTAGCACGGTCTTGGCTCACTGCAACCTCTGCCTCCCGAG T C ATAD2 Ensembl:ENSG00000156802 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1257969916 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86390,RMVar_hsa_circ_47794,RMVar_hsa_circ_254181,RMVar_hsa_circ_92139,RMVar_hsa_circ_266235,RMVar_hsa_circ_254188,RMVar_hsa_circ_115520,RMVar_hsa_circ_50757,RMVar_hsa_circ_254192,RMVar_hsa_circ_52754,RMVar_hsa_circ_45204,RMVar_hsa_circ_366710,RMVar_hsa_circ_338266,RMVar_hsa_circ_307644,RMVar_hsa_circ_328572,RMVar_hsa_circ_118569,RMVar_hsa_circ_254199,RMVar_hsa_circ_254200,RMVar_hsa_circ_254198,RMVar_hsa_circ_268865,RMVar_hsa_circ_344160,RMVar_hsa_circ_363412,RMVar_hsa_circ_374146,RMVar_hsa_circ_69779,RMVar_hsa_circ_254202,RMVar_hsa_circ_254203,RMVar_hsa_circ_254201 16131 RMVar_ID_16131 Human_SNP_ID_380739537 A-to-I Human chr8 - 123371800 123371800 123371800 AAGTGATTCCAGTTACTCGGTCATTGAGGGCTAGAAACATCGTTCAAAGTACAGAACACTTACAT AAGTGATTCCAGTTACTCGGTCATTGAGGGCTGGAAACATCGTTCAAAGTACAGAACACTTACAT T C ATAD2 Ensembl:ENSG00000156802 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1307130934 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1693126,Human_RBP_ID_9405756,Human_RBP_ID_16341529,Human_RBP_ID_26359359,Human_RBP_ID_27831560 Human_Splice_Rec_1005502,Human_Splice_Rec_1005554,Human_Splice_Rec_1005610,Human_Splice_Rec_1005664,Human_Splice_Rec_1005718 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_72393,RMVar_hsa_circ_254209,RMVar_hsa_circ_254211,RMVar_hsa_circ_354532,RMVar_hsa_circ_362895,RMVar_hsa_circ_353920,RMVar_hsa_circ_268202,RMVar_hsa_circ_354950,RMVar_hsa_circ_54047,RMVar_hsa_circ_366839,RMVar_hsa_circ_322108 16132 RMVar_ID_16132 Human_SNP_ID_380739900 A-to-I Human chr8 - 123373057 123373057 123373057 AAACCTCGTCTCTACTAAAAATCCAAAAAATTAGCCGGGCGAGATGACAGGAGCCTATAGTCCCA AAACCTCGTCTCTACTAAAAATCCAAAAAATTGGCCGGGCGAGATGACAGGAGCCTATAGTCCCA T C ATAD2 Ensembl:ENSG00000156802 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs188123669 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16341560 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_322108,RMVar_hsa_circ_364206 16133 RMVar_ID_16133 Human_SNP_ID_380739986 A-to-I Human chr8 - 123373324 123373324 123373324 TCAGTTATAGCCAGGTATGGTGGCTCATACCTATAATCCTAGCACTTTGGGAGGCTAAGGTGGGA TCAGTTATAGCCAGGTATGGTGGCTCATACCTGTAATCCTAGCACTTTGGGAGGCTAAGGTGGGA T C ATAD2 Ensembl:ENSG00000156802 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1477637882 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_254919 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_322108,RMVar_hsa_circ_364206 16134 RMVar_ID_16134 Human_SNP_ID_380740857 A-to-I Human chr8 - 123376929 123376929 123376929 CCCTACCACACCCAGCTAATTTTTGTATTTTTAGGAGGATAGGATTTCACCATGTTGGCCAGACT CCCTACCACACCCAGCTAATTTTTGTATTTTTGGGAGGATAGGATTTCACCATGTTGGCCAGACT T C ATAD2 Ensembl:ENSG00000156802 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1463758245 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7809423,Human_RBP_ID_16341719 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_322108,RMVar_hsa_circ_364206 16135 RMVar_ID_16135 Human_SNP_ID_380741325 A-to-I Human chr8 - 123378639 123378639 123378639 GGAATGCAGTGGCATGATCTCAGCTTACTGCAACCTCCGCCTCCCAGGTTCAAGCGATCCTCCTG GGAATGCAGTGGCATGATCTCAGCTTACTGCAGCCTCCGCCTCCCAGGTTCAAGCGATCCTCCTG T C ATAD2 Ensembl:ENSG00000156802 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1414007660 Functional Loss SNV dbSNP153 33..33 33 - - - 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_322108,RMVar_hsa_circ_364206 16136 RMVar_ID_16136 Human_SNP_ID_380745663 A-to-I Human chr8 - 123394629 123394629 123394629 AATACATAGGCTCTTTTTTTTTTCTTCGAGACAGAGTCTCACTCTCTCATCCAGGCTGGAGTGCA AATACATAGGCTCTTTTTTTTTTCTTCGAGACGGAGTCTCACTCTCTCATCCAGGCTGGAGTGCA T C ATAD2 Ensembl:ENSG00000156802 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs945185614 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1223510,Human_RBP_ID_7809609 16137 RMVar_ID_16137 Human_SNP_ID_380749036 A-to-I Human chr8 - 123407544 123407544 123407544 AATTTTTGTATTTTTAGTAGAGATGGGGTTTTACCATGTTGGCCCAGCTGGACTTGAACTCCTGA AATTTTTGTATTTTTAGTAGAGATGGGGTTTTGCCATGTTGGCCCAGCTGGACTTGAACTCCTGA T C ATAD2 Ensembl:ENSG00000156802 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs915382742 Functional Loss SNV dbSNP153 33..33 33 - - - 16138 RMVar_ID_16138 Human_SNP_ID_380755768 A-to-I Human chr8 + 123432167 123432167 123432167 GTGAGTAGTAGTGAGTAAAATTCGAGAACACTAAATCCTGAACCCCTTTCTAGATTTACTAAATC GTGAGTAGTAGTGAGTAAAATTCGAGAACACTGAATCCTGAACCCCTTTCTAGATTTACTAAATC A G WDYHV1 Ensembl:ENSG00000156795 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1044118375 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_323,RMVar_hsa_circ_330592,RMVar_hsa_circ_31555,RMVar_hsa_circ_254214 16139 RMVar_ID_16139 Human_SNP_ID_380758629 A-to-I Human chr8 + 123442743 123442743 123442743 CAGGCTGGAGTGCAGCGGCACGATCTCGGCTCACTGTAACCTCCACTTCCCAGGTTCAAGTGATT CAGGCTGGAGTGCAGCGGCACGATCTCGGCTCGCTGTAACCTCCACTTCCCAGGTTCAAGTGATT A G WDYHV1 Ensembl:ENSG00000156795 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs922643701 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_328282 16140 RMVar_ID_16140 Human_SNP_ID_380758630 A-to-I Human chr8 + 123442743 123442743 123442743 CAGGCTGGAGTGCAGCGGCACGATCTCGGCTCACTGTAACCTCCACTTCCCAGGTTCAAGTGATT CAGGCTGGAGTGCAGCGGCACGATCTCGGCTCTCTGTAACCTCCACTTCCCAGGTTCAAGTGATT A T WDYHV1 Ensembl:ENSG00000156795 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs922643701 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_328282 16141 RMVar_ID_16141 Human_SNP_ID_380761046 A-to-I Human chr8 + 123451591 123451591 123451591 GAACTCTTGACTTCAATTGGTCCGCCCACTTCAGCCTCCCAAAATGCTGGGATTACAGGCACGAG GAACTCTTGACTTCAATTGGTCCGCCCACTTCGGCCTCCCAAAATGCTGGGATTACAGGCACGAG A G WDYHV1 Ensembl:ENSG00000156795 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1010506595 Functional Loss SNV dbSNP153 33..33 33 - - - 16142 RMVar_ID_16142 Human_SNP_ID_380761693 A-to-I Human chr8 + 123454321 123454321 123454321 AGAAACAGTCATTCATAGTGAAGTTCTGCTATAATTGCTCCCTTGATAATAAATGGATGCAATTT AGAAACAGTCATTCATAGTGAAGTTCTGCTATGATTGCTCCCTTGATAATAAATGGATGCAATTT A G WDYHV1 Ensembl:ENSG00000156795 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs929681976 Functional Loss SNV dbSNP153 33..33 33 - - - 16143 RMVar_ID_16143 Human_SNP_ID_380761742 A-to-I Human chr8 + 123454461 123454461 123454461 TGCGATCTCAGCTCACCACAACTCCACCTCCCAGGTTCAAGCAATTCTCCTGCCCCAGCCTCCCG TGCGATCTCAGCTCACCACAACTCCACCTCCCGGGTTCAAGCAATTCTCCTGCCCCAGCCTCCCG A G WDYHV1 Ensembl:ENSG00000156795 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968850223 Functional Loss SNV dbSNP153 33..33 33 - - - 16144 RMVar_ID_16144 Human_SNP_ID_380761777 A-to-I Human chr8 + 123454590 123454590 123454590 CGGGGTTTCTCCATGTTGGTCGGGCTGGTCTCAAACGCCTGACCTCAGGTGTAGCAGTCGGAGAT CGGGGTTTCTCCATGTTGGTCGGGCTGGTCTCTAACGCCTGACCTCAGGTGTAGCAGTCGGAGAT A T WDYHV1 Ensembl:ENSG00000156795 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1057134173 Functional Loss SNV dbSNP153 33..33 33 - - - 16145 RMVar_ID_16145 Human_SNP_ID_380846407 A-to-I Human chr8 + 123803122 123803122 123803122 GCCCAGAAGTTGGAGACCAACTTGGATAACATAGTGAAACCCTGTCTTAATTTATAGTAACAAAT GCCCAGAAGTTGGAGACCAACTTGGATAACATGGTGAAACCCTGTCTTAATTTATAGTAACAAAT A G FAM91A1 Ensembl:ENSG00000176853 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886612997 Functional Loss SNV dbSNP153 33..33 33 - - - 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 16146 RMVar_ID_16146 Human_SNP_ID_380846493 A-to-I Human chr8 + 123803452 123803452 123803452 CCTGCCTTAGCCTCCAGAGTAGCTGGGACTACAAGCTCACGCCACCATGCCTGGCTAATTTTTTA CCTGCCTTAGCCTCCAGAGTAGCTGGGACTACCAGCTCACGCCACCATGCCTGGCTAATTTTTTA A C FAM91A1 Ensembl:ENSG00000176853 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978979946 Functional Loss SNV dbSNP153 33..33 33 - - - 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 16147 RMVar_ID_16147 Human_SNP_ID_381009475 A-to-I Human chr8 + 124482773 124482773 124482773 ACGTGGAAAAACCCTGTCTCTACTGAAAATGCAAAATTAGCTGGGAGTGGTGGTACATACCTGTA ACGTGGAAAAACCCTGTCTCTACTGAAAATGCTAAATTAGCTGGGAGTGGTGGTACATACCTGTA A T RNF139 Ensembl:ENSG00000170881 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs949439939 Functional Loss SNV dbSNP153 33..33 33 - - - 16148 RMVar_ID_16148 Human_SNP_ID_381011665 A-to-I Human chr8 - 124489538 124489538 124489538 GTGATGGCAGGTGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCCA GTGATGGCAGGTGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCCA T C TATDN1 Ensembl:ENSG00000147687 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1487093051 Functional Loss SNV dbSNP153 33..33 33 - - - 16149 RMVar_ID_16149 Human_SNP_ID_381011666 A-to-I Human chr8 - 124489542 124489539 124489542 GGGTGTGATGGCAGGTGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAA GGGTGTGATGGCAGGTGCCTGTAATCCCAGCT___CAGGAGGCTGAGGCAGGAGAATCACTTGAA GAGT G TATDN1 Ensembl:ENSG00000147687 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1241824364 Functional Loss DEL dbSNP153 33..35 33 - - - 16150 RMVar_ID_16150 Human_SNP_ID_381011673 A-to-I Human chr8 + 124489594 124489594 124489594 TGCCATCACACCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACTATGTTGGCTGGCC TGCCATCACACCCAGCTAATTTTTGTATTTTTCGTAGAGACGGGGTTTCACTATGTTGGCTGGCC A C AC090198.1 Ensembl:ENSG00000253106 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978681613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7873965 16151 RMVar_ID_16151 Human_SNP_ID_381012338 A-to-I Human chr8 - 124492281 124492281 124492281 GTGTTTTTAAATGTAGACTGTTTAAGAACTATAAAGGCTGGCCAGGCATGGTGGCTCACATCTGT GTGTTTTTAAATGTAGACTGTTTAAGAACTATGAAGGCTGGCCAGGCATGGTGGCTCACATCTGT T C TATDN1 Ensembl:ENSG00000147687 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7005861 Functional Loss SNV dbSNP153 33..33 33 - - - 16152 RMVar_ID_16152 Human_SNP_ID_381017224 A-to-I Human chr8 - 124512231 124512231 124512231 TTTAGTAGAGACAGAGTTTCACCATGTTGGCCAGGCTGGTTTCGAACTCCAGACCTCAAGTGATC TTTAGTAGAGACAGAGTTTCACCATGTTGGCCGGGCTGGTTTCGAACTCCAGACCTCAAGTGATC T C TATDN1 Ensembl:ENSG00000147687 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1381132829 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14290,RMVar_hsa_circ_338522,RMVar_hsa_circ_293993,RMVar_hsa_circ_71373,RMVar_hsa_circ_350417,RMVar_hsa_circ_254242,RMVar_hsa_circ_368831,RMVar_hsa_circ_15160,RMVar_hsa_circ_372735,RMVar_hsa_circ_307075,RMVar_hsa_circ_254243,RMVar_hsa_circ_254244,RMVar_hsa_circ_315921,RMVar_hsa_circ_286398,RMVar_hsa_circ_254247,RMVar_hsa_circ_280044,RMVar_hsa_circ_254245,RMVar_hsa_circ_375023,RMVar_hsa_circ_266125,RMVar_hsa_circ_254246 16153 RMVar_ID_16153 Human_SNP_ID_381018389 A-to-I Human chr8 - 124517365 124517365 124517365 GGAGTGCAATGGCACGATCTCGGCTCACGGCAACCTCTGCCTCCTGGGTACAAGTGATTCTCCTG GGAGTGCAATGGCACGATCTCGGCTCACGGCAGCCTCTGCCTCCTGGGTACAAGTGATTCTCCTG T C TATDN1 Ensembl:ENSG00000147687 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985413760 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71373,RMVar_hsa_circ_368831,RMVar_hsa_circ_15160,RMVar_hsa_circ_307075,RMVar_hsa_circ_254243,RMVar_hsa_circ_254244,RMVar_hsa_circ_315921,RMVar_hsa_circ_286398,RMVar_hsa_circ_125849,RMVar_hsa_circ_254245,RMVar_hsa_circ_375023,RMVar_hsa_circ_266125,RMVar_hsa_circ_254246,RMVar_hsa_circ_377692,RMVar_hsa_circ_254249 16154 RMVar_ID_16154 Human_SNP_ID_381018565 A-to-I Human chr8 - 124517967 124517967 124517967 GACCTCGTGATCCGCCTGCCTCGGCCTCCCAAAGCGCTGGGATTACAGGCGTGAGCCACCGTGCC GACCTCGTGATCCGCCTGCCTCGGCCTCCCAAGGCGCTGGGATTACAGGCGTGAGCCACCGTGCC T C TATDN1 Ensembl:ENSG00000147687 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1159883370 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71373,RMVar_hsa_circ_368831,RMVar_hsa_circ_15160,RMVar_hsa_circ_307075,RMVar_hsa_circ_254243,RMVar_hsa_circ_254244,RMVar_hsa_circ_315921,RMVar_hsa_circ_286398,RMVar_hsa_circ_125849,RMVar_hsa_circ_254245,RMVar_hsa_circ_375023,RMVar_hsa_circ_266125,RMVar_hsa_circ_254246,RMVar_hsa_circ_377692,RMVar_hsa_circ_254249 16155 RMVar_ID_16155 Human_SNP_ID_381018584 A-to-I Human chr8 - 124518023 124518023 124518023 TATTTTTAGTAGAGAAGGGGTTTCACTGTGTTAGCCAAGATGGGTCTTGATCTCCTGACCTCGTG TATTTTTAGTAGAGAAGGGGTTTCACTGTGTTGGCCAAGATGGGTCTTGATCTCCTGACCTCGTG T C TATDN1 Ensembl:ENSG00000147687 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1180723619 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71373,RMVar_hsa_circ_368831,RMVar_hsa_circ_15160,RMVar_hsa_circ_307075,RMVar_hsa_circ_254243,RMVar_hsa_circ_254244,RMVar_hsa_circ_315921,RMVar_hsa_circ_286398,RMVar_hsa_circ_125849,RMVar_hsa_circ_254245,RMVar_hsa_circ_375023,RMVar_hsa_circ_266125,RMVar_hsa_circ_254246,RMVar_hsa_circ_377692,RMVar_hsa_circ_254249 16156 RMVar_ID_16156 Human_SNP_ID_381024681 A-to-I Human chr8 + 124542190 124542190 124542190 CCCCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCATGCCCGGCCTCATTTT CCCCTGCCTTGGCCTCCCAAAGTGCTGGGATTTCAGGCGTGAGCCACCATGCCCGGCCTCATTTT A T NDUFB9 Ensembl:ENSG00000147684 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1173526788 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84487,RMVar_hsa_circ_254251 16157 RMVar_ID_16157 Human_SNP_ID_381024714 A-to-I Human chr8 + 124542326 124542326 124542326 CACACGCCTTGGCCTCCCAACGTGCTGGGATTACAGGTGTGAGCCACCGCACCTGACCAGAAGAC CACACGCCTTGGCCTCCCAACGTGCTGGGATTGCAGGTGTGAGCCACCGCACCTGACCAGAAGAC A G NDUFB9 Ensembl:ENSG00000147684 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs577837606 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84487,RMVar_hsa_circ_254251 16158 RMVar_ID_16158 Human_SNP_ID_381057124 A-to-I Human chr8 - 124674385 124674385 124674385 AGGCTGACAGCTCCTGGCGATGCGTGGGGTGTACCATATATAGTGACGCTGATGCAGATTATGCA AGGCTGACAGCTCCTGGCGATGCGTGGGGTGTGCCATATATAGTGACGCTGATGCAGATTATGCA T C MTSS1 Ensembl:ENSG00000170873 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs750824634 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55907,RMVar_hsa_circ_254259,RMVar_hsa_circ_91018 16159 RMVar_ID_16159 Human_SNP_ID_381057394 A-to-I Human chr8 - 124675515 124675515 124675515 CTGAATCGTTCACTTCAAAGTGATTTTGTCTTATGTCAATTTCACTTCAAAATATAAAACACACA CTGAATCGTTCACTTCAAAGTGATTTTGTCTTGTGTCAATTTCACTTCAAAATATAAAACACACA T C MTSS1 Ensembl:ENSG00000170873 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs763844828 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55907,RMVar_hsa_circ_254259,RMVar_hsa_circ_91018 16160 RMVar_ID_16160 Human_SNP_ID_381142240 A-to-I Human chr8 - 125033591 125033591 125033591 TGAGCCGAGATTGTGCCACTGCCCTCCAGCCTAGGTGACATAGTGAGCTCCGTCTCAAAAAAAAA TGAGCCGAGATTGTGCCACTGCCCTCCAGCCTGGGTGACATAGTGAGCTCCGTCTCAAAAAAAAA T C WASHC5 Ensembl:ENSG00000164961 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1180267011 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73572,RMVar_hsa_circ_118628,RMVar_hsa_circ_254280,RMVar_hsa_circ_98024,RMVar_hsa_circ_254279,RMVar_hsa_circ_254281 16161 RMVar_ID_16161 Human_SNP_ID_381142272 A-to-I Human chr8 - 125033731 125033731 125033731 CCAGCCTGGTCAACATAGTGAAACCCGTCTCTACTAAAAACACAAAAATTAGCCAGACGTGGTGG CCAGCCTGGTCAACATAGTGAAACCCGTCTCTGCTAAAAACACAAAAATTAGCCAGACGTGGTGG T C WASHC5 Ensembl:ENSG00000164961 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs916412839 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73572,RMVar_hsa_circ_118628,RMVar_hsa_circ_254280,RMVar_hsa_circ_98024,RMVar_hsa_circ_254279,RMVar_hsa_circ_254281 16162 RMVar_ID_16162 Human_SNP_ID_381142435 A-to-I Human chr8 - 125034497 125034497 125034497 CATTTTAGCCATTCTTTTTTTTTTTCTGAAACAGAGTCTCACTCTGTCACCCAGGCTGAAGTGCA CATTTTAGCCATTCTTTTTTTTTTTCTGAAACGGAGTCTCACTCTGTCACCCAGGCTGAAGTGCA T C WASHC5 Ensembl:ENSG00000164961 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1184443880 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73572,RMVar_hsa_circ_118628,RMVar_hsa_circ_254280,RMVar_hsa_circ_98024,RMVar_hsa_circ_254279,RMVar_hsa_circ_254281 16163 RMVar_ID_16163 Human_SNP_ID_381147387 A-to-I Human chr8 - 125055266 125055266 125055266 GGCATACAACACCACACCCAGCTAATTTTTGTATTTTTAATAGAGACGAGTTTCACCATGTTGGC GGCATACAACACCACACCCAGCTAATTTTTGTGTTTTTAATAGAGACGAGTTTCACCATGTTGGC T C WASHC5 Ensembl:ENSG00000164961 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs528901166 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10599,RMVar_hsa_circ_4608,RMVar_hsa_circ_98024,RMVar_hsa_circ_254279,RMVar_hsa_circ_329235,RMVar_hsa_circ_254283,RMVar_hsa_circ_5173,RMVar_hsa_circ_48988,RMVar_hsa_circ_377543,RMVar_hsa_circ_254284,RMVar_hsa_circ_328428,RMVar_hsa_circ_254286,RMVar_hsa_circ_27895,RMVar_hsa_circ_29839,RMVar_hsa_circ_302768,RMVar_hsa_circ_254288,RMVar_hsa_circ_254289 16164 RMVar_ID_16164 Human_SNP_ID_381151566 A-to-I Human chr8 - 125072084 125072084 125072084 TGCCCACCTCGGCCTCCCAAAGTGCTAGGATTATAGGTCTGAGCCACCATGCCCAGCCTGTAAAT TGCCCACCTCGGCCTCCCAAAGTGCTAGGATTGTAGGTCTGAGCCACCATGCCCAGCCTGTAAAT T C WASHC5 Ensembl:ENSG00000164961 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1033890888 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4608,RMVar_hsa_circ_5173,RMVar_hsa_circ_48988,RMVar_hsa_circ_377543,RMVar_hsa_circ_254284,RMVar_hsa_circ_328428,RMVar_hsa_circ_254286,RMVar_hsa_circ_27895,RMVar_hsa_circ_29839,RMVar_hsa_circ_31640,RMVar_hsa_circ_45916,RMVar_hsa_circ_254289,RMVar_hsa_circ_16691,RMVar_hsa_circ_57329,RMVar_hsa_circ_26087,RMVar_hsa_circ_69047,RMVar_hsa_circ_73443 16165 RMVar_ID_16165 Human_SNP_ID_381151731 A-to-I Human chr8 - 125072577 125072577 125072577 TTGAGCCCAGGAGTTCAGAACCAGCCTGGGTAACACAGTGAGATCCCATCTCTACAAAAAGTAAA TTGAGCCCAGGAGTTCAGAACCAGCCTGGGTATCACAGTGAGATCCCATCTCTACAAAAAGTAAA T A WASHC5 Ensembl:ENSG00000164961 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1241479177 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4608,RMVar_hsa_circ_5173,RMVar_hsa_circ_48988,RMVar_hsa_circ_377543,RMVar_hsa_circ_254284,RMVar_hsa_circ_328428,RMVar_hsa_circ_254286,RMVar_hsa_circ_27895,RMVar_hsa_circ_29839,RMVar_hsa_circ_31640,RMVar_hsa_circ_45916,RMVar_hsa_circ_254289,RMVar_hsa_circ_16691,RMVar_hsa_circ_57329,RMVar_hsa_circ_26087,RMVar_hsa_circ_69047,RMVar_hsa_circ_73443 16166 RMVar_ID_16166 Human_SNP_ID_381186927 A-to-I Human chr8 + 125223191 125223191 125223191 CAACCTGAGCAACATGGTGAAATCCCATCTGTACAAAAAATACAAAAAAATTAGCCAGACATGGT CAACCTGAGCAACATGGTGAAATCCCATCTGTTCAAAAAATACAAAAAAATTAGCCAGACATGGT A T NSMCE2 Ensembl:ENSG00000156831 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs911183794 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 16167 RMVar_ID_16167 Human_SNP_ID_381192169 A-to-I Human chr8 + 125246373 125246373 125246373 GCCCGACTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGTCCAGCTGCTCTCGA GCCCGACTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGTCCAGCTGCTCTCGA A G NSMCE2 Ensembl:ENSG00000156831 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs995705887 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 16168 RMVar_ID_16168 Human_SNP_ID_381193198 A-to-I Human chr8 + 125250750 125250750 125250750 ATAGCTTACTGCAGCCTCACCCTCCCCAGCTCAAGAGATCCTCCAACCTCAGCCTCCCAAGTAGC ATAGCTTACTGCAGCCTCACCCTCCCCAGCTCTAGAGATCCTCCAACCTCAGCCTCCCAAGTAGC A T NSMCE2 Ensembl:ENSG00000156831 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017912748 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 16169 RMVar_ID_16169 Human_SNP_ID_381194904 A-to-I Human chr8 + 125257673 125257673 125257673 CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCTCACCACCATGCCTGTCGAATTTTT CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTGCAGGCGCTCACCACCATGCCTGTCGAATTTTT A G NSMCE2 Ensembl:ENSG00000156831 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264928242 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_179426 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 16170 RMVar_ID_16170 Human_SNP_ID_381194933 A-to-I Human chr8 + 125257741 125257741 125257741 TATTTTTAGTAGAAACGGGGTTTCATTGTGTTAGCCAGGATGGTCTCGATCTCCTGACTTCATTA TATTTTTAGTAGAAACGGGGTTTCATTGTGTTGGCCAGGATGGTCTCGATCTCCTGACTTCATTA A G NSMCE2 Ensembl:ENSG00000156831 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1186523361 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 16171 RMVar_ID_16171 Human_SNP_ID_381196478 A-to-I Human chr8 + 125264556 125264556 125264556 GGCCTCCTGAGTACCTGGGACCATCTGCGCGCACCACCACGCCCTGCTAATTTTTGTATTTTTAG GGCCTCCTGAGTACCTGGGACCATCTGCGCGCCCCACCACGCCCTGCTAATTTTTGTATTTTTAG A C NSMCE2 Ensembl:ENSG00000156831 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1452212177 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16349715 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 16172 RMVar_ID_16172 Human_SNP_ID_381198077 A-to-I Human chr8 + 125271209 125271209 125271209 CTTGAACCTGGGAGGTGGAGGTTGCAGTGAGCAGAGATTATGCCATTGCACTGCAGACTGGGCGA CTTGAACCTGGGAGGTGGAGGTTGCAGTGAGCCGAGATTATGCCATTGCACTGCAGACTGGGCGA A C NSMCE2 Ensembl:ENSG00000156831 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs986209845 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 16173 RMVar_ID_16173 Human_SNP_ID_381222292 A-to-I Human chr8 + 125372657 125372657 125372657 AAAATTAGCCAGGCATGGTGATATGTGCCTGTAATTCCAGCTACTTGGGAGGCTGAGGCAGGAGA AAAATTAGCCAGGCATGGTGATATGTGCCTGTGATTCCAGCTACTTGGGAGGCTGAGGCAGGAGA A G RF00017-2064 RNACentral:URS000098196C SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs962559202 Functional Loss SNV dbSNP153 33..33 33 - - - 16174 RMVar_ID_16174 Human_SNP_ID_381535159 A-to-I Human chr8 + 126634599 126634599 126634599 AATATCTCACCCAGTTATTGCTGGGATTCCCCAGGAACATTACATGGGAACATATCGCCATATAG AATATCTCACCCAGTTATTGCTGGGATTCCCCGGGAACATTACATGGGAACATATCGCCATATAG A G PCAT1 Ensembl:ENSG00000253438 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1292881733 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1007898 16175 RMVar_ID_16175 Human_SNP_ID_381669285 A-to-I Human chr8 - 127158467 127158467 127158467 ATTCAAGCAATCTGCCTGCCTTGGCCTCCCAAAGTGTTGGGATTACAGGTGTGAGCCACCATGCC ATTCAAGCAATCTGCCTGCCTTGGCCTCCCAAGGTGTTGGGATTACAGGTGTGAGCCACCATGCC T C CASC19 Ensembl:ENSG00000254166 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1281862981 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8803,RMVar_hsa_circ_354496,RMVar_hsa_circ_356869,RMVar_hsa_circ_340463,RMVar_hsa_circ_36683 16176 RMVar_ID_16176 Human_SNP_ID_381674965 A-to-I Human chr8 - 127180886 127180886 127180886 AGACTTCTGGGCTCAAGCAATCCTCCTGCCTCAGCCTCCCAAAGTGTTTGGATTATAGGCATGAG AGACTTCTGGGCTCAAGCAATCCTCCTGCCTCGGCCTCCCAAAGTGTTTGGATTATAGGCATGAG T C CASC19 Ensembl:ENSG00000254166 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1231878505 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_356869,RMVar_hsa_circ_52506,RMVar_hsa_circ_366207,RMVar_hsa_circ_53106,RMVar_hsa_circ_43455,RMVar_hsa_circ_36406,RMVar_hsa_circ_332735,RMVar_hsa_circ_56791,RMVar_hsa_circ_365319,RMVar_hsa_circ_349541,RMVar_hsa_circ_58607 16177 RMVar_ID_16177 Human_SNP_ID_381675639 A-to-I Human chr8 - 127183438 127183438 127183438 ATGGGTAGACTGCAAAAATTTTCTCCCATTCTATAGGTTGCTTGTTCACTATGGTGATAATTTCT ATGGGTAGACTGCAAAAATTTTCTCCCATTCTGTAGGTTGCTTGTTCACTATGGTGATAATTTCT T C CASC19 Ensembl:ENSG00000254166 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs551821312 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3137412 RMVar_hsa_circ_356869,RMVar_hsa_circ_52506,RMVar_hsa_circ_366207,RMVar_hsa_circ_53106,RMVar_hsa_circ_43455,RMVar_hsa_circ_36406,RMVar_hsa_circ_332735,RMVar_hsa_circ_56791,RMVar_hsa_circ_365319,RMVar_hsa_circ_349541,RMVar_hsa_circ_58607 16178 RMVar_ID_16178 Human_SNP_ID_381684918 A-to-I Human chr8 - 127219719 127219719 127219719 TTAATTGCAGTCATTTACATGGTAGATTCTCTATAATCATTTAATTTGCTATAGGTCTATGATTT TTAATTGCAGTCATTTACATGGTAGATTCTCTGTAATCATTTAATTTGCTATAGGTCTATGATTT T C CASC19 Ensembl:ENSG00000254166 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006424567 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3138627,Human_RBP_ID_7871282,Human_RBP_ID_8680279,Human_RBP_ID_16352329,Human_RBP_ID_17200778,Human_RBP_ID_21564118,Human_RBP_ID_26152053 RMVar_hsa_circ_337858 16179 RMVar_ID_16179 Human_SNP_ID_381686667 A-to-I Human chr8 + 127226036 127226036 127226036 GAGAAGATCACTTTAGCACAGAAATTCTAGACAAACCTGGGCAAGATGGTGACACCCTGTCTCTA GAGAAGATCACTTTAGCACAGAAATTCTAGACGAACCTGGGCAAGATGGTGACACCCTGTCTCTA A G PCAT1 Ensembl:ENSG00000253438 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1015953527 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3139009 16180 RMVar_ID_16180 Human_SNP_ID_381692999 A-to-I Human chr8 + 127250987 127250987 127250987 TGCAGGTGACAGGTGTCTGAGTAGCTGAAAACACAAGCTTTAGACCCAGGCAACTCTAAATATGA TGCAGGTGACAGGTGTCTGAGTAGCTGAAAACCCAAGCTTTAGACCCAGGCAACTCTAAATATGA A C PCAT1 Ensembl:ENSG00000253438 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1450856649 Functional Loss SNV dbSNP153 33..33 33 - - - 16181 RMVar_ID_16181 Human_SNP_ID_381693109 A-to-I Human chr8 + 127251385 127251385 127251385 GCCACTGCAACCAGCCCAAGCTTGATATTTTTATACCCATTTTACAAATGAAAAAGTGGTGGCTC GCCACTGCAACCAGCCCAAGCTTGATATTTTTGTACCCATTTTACAAATGAAAAAGTGGTGGCTC A G PCAT1 Ensembl:ENSG00000253438 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1405398045 Functional Loss SNV dbSNP153 33..33 33 - - - 16182 RMVar_ID_16182 Human_SNP_ID_381815774 A-to-I Human chr8 + 127738287 127738287 127738287 CCGCGACGATGCCCCTCAACGTTAGCTTCACCAACAGGAACTATGACCTCGACTACGACTCGGTG CCGCGACGATGCCCCTCAACGTTAGCTTCACCTACAGGAACTATGACCTCGACTACGACTCGGTG A T MYC Ensembl:ENSG00000136997 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1490644442 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5628628 Human_Splice_Rec_1008884,Human_Splice_Rec_1008890,Human_Splice_Rec_1008892,Human_Splice_Rec_1008896,Human_Splice_Rec_1008900,Human_Splice_Rec_1008906,Human_Splice_Rec_1008910 RMVar_hsa_circ_76158,RMVar_hsa_circ_254316,RMVar_hsa_circ_85506,RMVar_hsa_circ_254317 16183 RMVar_ID_16183 Human_SNP_ID_381832551 A-to-I Human chr8 + 127798755 127798755 127798755 AAAATTAGCCCGGCGTGGTGGCACACGCCTGTAGTCCTAGCTACTCGGGAGGCTGAGGTAGGAAG AAAATTAGCCCGGCGTGGTGGCACACGCCTGTCGTCCTAGCTACTCGGGAGGCTGAGGTAGGAAG A C PVT1 Ensembl:ENSG00000249859 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs920789159 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118838,RMVar_hsa_circ_101526,RMVar_hsa_circ_118329,RMVar_hsa_circ_254318,RMVar_hsa_circ_254319,RMVar_hsa_circ_254320 16184 RMVar_ID_16184 Human_SNP_ID_381832552 A-to-I Human chr8 + 127798755 127798755 127798755 AAAATTAGCCCGGCGTGGTGGCACACGCCTGTAGTCCTAGCTACTCGGGAGGCTGAGGTAGGAAG AAAATTAGCCCGGCGTGGTGGCACACGCCTGTTGTCCTAGCTACTCGGGAGGCTGAGGTAGGAAG A T PVT1 Ensembl:ENSG00000249859 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs920789159 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118838,RMVar_hsa_circ_101526,RMVar_hsa_circ_118329,RMVar_hsa_circ_254318,RMVar_hsa_circ_254319,RMVar_hsa_circ_254320 16185 RMVar_ID_16185 Human_SNP_ID_381833334 A-to-I Human chr8 + 127802015 127802015 127802015 TCGGCTCATTGCAACTTCCGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGC TCGGCTCATTGCAACTTCCGCCTCCCGGGTTCCAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGC A C PVT1 Ensembl:ENSG00000249859 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202536737 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118838,RMVar_hsa_circ_101526,RMVar_hsa_circ_118329,RMVar_hsa_circ_254318,RMVar_hsa_circ_254319,RMVar_hsa_circ_254320 16186 RMVar_ID_16186 Human_SNP_ID_381833985 A-to-I Human chr8 + 127804095 127804095 127804095 CTGTAGTTCCATCTTTGGTGGCACGCACCTGTATTCCCATCTACTTGGGAGGCTGAGGCAGGAAG CTGTAGTTCCATCTTTGGTGGCACGCACCTGTTTTCCCATCTACTTGGGAGGCTGAGGCAGGAAG A T PVT1 Ensembl:ENSG00000249859 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1185605648 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17578740 RMVar_hsa_circ_118838,RMVar_hsa_circ_101526,RMVar_hsa_circ_118329,RMVar_hsa_circ_254318,RMVar_hsa_circ_254319,RMVar_hsa_circ_254320 16187 RMVar_ID_16187 Human_SNP_ID_381834501 A-to-I Human chr8 + 127806205 127806205 127806205 AAGTAGATGGCTGGGCACCGTGGCTCATGCCTATAATCCCAGCACTTTGGAAGGCTGAGGCGGGC AAGTAGATGGCTGGGCACCGTGGCTCATGCCTGTAATCCCAGCACTTTGGAAGGCTGAGGCGGGC A G PVT1 Ensembl:ENSG00000249859 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1393615825 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26152344 RMVar_hsa_circ_118838,RMVar_hsa_circ_101526,RMVar_hsa_circ_118329,RMVar_hsa_circ_254318,RMVar_hsa_circ_254319,RMVar_hsa_circ_254320 16188 RMVar_ID_16188 Human_SNP_ID_381834563 A-to-I Human chr8 + 127806406 127806406 127806406 TCGCTTGAACCTGGGAGGCATAGGTTGCAGTGAACCCAGATCTTGCCACTGCATGCCAGCCTGGA TCGCTTGAACCTGGGAGGCATAGGTTGCAGTGTACCCAGATCTTGCCACTGCATGCCAGCCTGGA A T PVT1 Ensembl:ENSG00000249859 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350297827 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8680482,Human_RBP_ID_16353327 RMVar_hsa_circ_118838,RMVar_hsa_circ_101526,RMVar_hsa_circ_118329,RMVar_hsa_circ_254318,RMVar_hsa_circ_254319,RMVar_hsa_circ_254320 16189 RMVar_ID_16189 Human_SNP_ID_381835080 A-to-I Human chr8 + 127808752 127808752 127808752 TATTTTGGAGACAGAAAGGACTTCTTGGGACCAGGCGTGGTGGCTCATGCCTGTAATCCCAGCAC TATTTTGGAGACAGAAAGGACTTCTTGGGACCGGGCGTGGTGGCTCATGCCTGTAATCCCAGCAC A G PVT1 Ensembl:ENSG00000249859 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1245303486 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3888298,Human_RBP_ID_23315906 RMVar_hsa_circ_118838,RMVar_hsa_circ_101526,RMVar_hsa_circ_118329,RMVar_hsa_circ_254318,RMVar_hsa_circ_254319,RMVar_hsa_circ_254320 16190 RMVar_ID_16190 Human_SNP_ID_381836072 A-to-I Human chr8 + 127812313 127812313 127812313 AGGAAGGAAGAGAATGAAAGGCTGGGCGTGGTAGCTCTTGCCTGTTGTAGTCCTGGCACTTTGGG AGGAAGGAAGAGAATGAAAGGCTGGGCGTGGTGGCTCTTGCCTGTTGTAGTCCTGGCACTTTGGG A G PVT1 Ensembl:ENSG00000249859 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) 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 16191 RMVar_ID_16191 Human_SNP_ID_381836076 A-to-I Human chr8 + 127812329 127812329 127812329 AAAGGCTGGGCGTGGTAGCTCTTGCCTGTTGTAGTCCTGGCACTTTGGGAGGCTGAGATGGGAGG AAAGGCTGGGCGTGGTAGCTCTTGCCTGTTGTCGTCCTGGCACTTTGGGAGGCTGAGATGGGAGG A C PVT1 Ensembl:ENSG00000249859 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459044425 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8680489,Human_RBP_ID_16353525,Human_RBP_ID_24391946 RMVar_hsa_circ_118838,RMVar_hsa_circ_101526,RMVar_hsa_circ_118329,RMVar_hsa_circ_254318,RMVar_hsa_circ_254319,RMVar_hsa_circ_254320 16192 RMVar_ID_16192 Human_SNP_ID_381836496 A-to-I Human chr8 + 127813876 127813876 127813876 ACGATCTCGGCTCACTGCACCCTCTGCCTTCCAGGTTCAAGCAATTCTTCTGCCTCAGCCTTCTG ACGATCTCGGCTCACTGCACCCTCTGCCTTCCGGGTTCAAGCAATTCTTCTGCCTCAGCCTTCTG A G PVT1 Ensembl:ENSG00000249859 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1370592843 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5105668,Human_RBP_ID_5251562,Human_RBP_ID_16353572 RMVar_hsa_circ_118838,RMVar_hsa_circ_101526,RMVar_hsa_circ_118329,RMVar_hsa_circ_254318,RMVar_hsa_circ_254319,RMVar_hsa_circ_254320 16193 RMVar_ID_16193 Human_SNP_ID_381839329 A-to-I Human chr8 + 127824864 127824864 127824864 TAATGTGGCCGGGCATGAAGGCTCCTGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGTGG TAATGTGGCCGGGCATGAAGGCTCCTGCCTGTTATCCCAGCACTTTGGGAGGCCGAGGTGGGTGG A T PVT1 Ensembl:ENSG00000249859 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1005458957 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118838,RMVar_hsa_circ_101526,RMVar_hsa_circ_118329,RMVar_hsa_circ_254318,RMVar_hsa_circ_254319,RMVar_hsa_circ_254320 16194 RMVar_ID_16194 Human_SNP_ID_381839365 A-to-I Human chr8 + 127825045 127825045 127825045 GGAAGGCTAAGGCTGGAAAATCATTTGAACCCAGGAGGTGGAGGTTGCAGTGAGTCGAGATCATG GGAAGGCTAAGGCTGGAAAATCATTTGAACCCGGGAGGTGGAGGTTGCAGTGAGTCGAGATCATG A G PVT1 Ensembl:ENSG00000249859 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs957351624 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118838,RMVar_hsa_circ_101526,RMVar_hsa_circ_118329,RMVar_hsa_circ_254318,RMVar_hsa_circ_254319,RMVar_hsa_circ_254320 16195 RMVar_ID_16195 Human_SNP_ID_381847503 A-to-I Human chr8 + 127857016 127857016 127857016 GGGAGGCCGAGGCAGGTGGATTGCTTGAGGTCAGAAGTTCGAGACCAGCCTGGCCAACATGGCGA GGGAGGCCGAGGCAGGTGGATTGCTTGAGGTCGGAAGTTCGAGACCAGCCTGGCCAACATGGCGA A G PVT1 Ensembl:ENSG00000249859 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1203933224 Functional Loss SNV dbSNP153 33..33 33 - - - 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 16196 RMVar_ID_16196 Human_SNP_ID_381847766 A-to-I Human chr8 + 127858133 127858133 127858133 TGGTCTTAGGCTGGGTGTGGTGGCTCATGCCTATAATCACGGCACTTTGGGAGGCCAAGGCGGCT TGGTCTTAGGCTGGGTGTGGTGGCTCATGCCTGTAATCACGGCACTTTGGGAGGCCAAGGCGGCT A G PVT1 Ensembl:ENSG00000249859 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs562244909 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8274745 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 16197 RMVar_ID_16197 Human_SNP_ID_381847825 A-to-I Human chr8 + 127858322 127858322 127858322 CCAGCTACCAGGGAGGCTGAGGCAGGAGAATCACTTGAACCTGGGAGGCGGAGGTTGCAGTGAGC CCAGCTACCAGGGAGGCTGAGGCAGGAGAATCGCTTGAACCTGGGAGGCGGAGGTTGCAGTGAGC A G PVT1 Ensembl:ENSG00000249859 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025523815 Functional Loss SNV dbSNP153 33..33 33 - - - 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 16198 RMVar_ID_16198 Human_SNP_ID_381848646 A-to-I Human chr8 + 127861347 127861347 127861347 AGCATGGGTGCAGGCTGGGCGCCGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGC AGCATGGGTGCAGGCTGGGCGCCGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGC A G PVT1 Ensembl:ENSG00000249859 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs936583913 Functional Loss SNV dbSNP153 33..33 33 - - - 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 16199 RMVar_ID_16199 Human_SNP_ID_381848923 A-to-I Human chr8 + 127862628 127862628 127862628 TATTTTTTGTACACATGAGGTCTCACTATGTTACCAGGCTGGTCTCAAACTCCTGGCCTCGGGCA TATTTTTTGTACACATGAGGTCTCACTATGTTGCCAGGCTGGTCTCAAACTCCTGGCCTCGGGCA A G PVT1 Ensembl:ENSG00000249859 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs771802146 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5105735,Human_RBP_ID_17578747 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 16200 RMVar_ID_16200 Human_SNP_ID_381872491 A-to-I Human chr8 + 127956584 127956584 127956584 TCGGCTCACTGTAACCTCTGCCTCCTGAGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGC TCGGCTCACTGTAACCTCTGCCTCCTGAGTTCCAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGC A C PVT1 Ensembl:ENSG00000249859 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1022057615 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75888,RMVar_hsa_circ_118838,RMVar_hsa_circ_101526,RMVar_hsa_circ_254319,RMVar_hsa_circ_254320,RMVar_hsa_circ_107291,RMVar_hsa_circ_254322,RMVar_hsa_circ_369306,RMVar_hsa_circ_111912,RMVar_hsa_circ_115647,RMVar_hsa_circ_254324,RMVar_hsa_circ_254325,RMVar_hsa_circ_371319,RMVar_hsa_circ_373231,RMVar_hsa_circ_254323,RMVar_hsa_circ_296671,RMVar_hsa_circ_254330,RMVar_hsa_circ_254332,RMVar_hsa_circ_254333,RMVar_hsa_circ_254331 16201 RMVar_ID_16201 Human_SNP_ID_381876669 A-to-I Human chr8 + 127972982 127972982 127972982 GTTGGAGTGCAGTGATGTAATCATAGCTCACTATAACCTCGAACTACTGGCTTCAAGCAATCCTC GTTGGAGTGCAGTGATGTAATCATAGCTCACTGTAACCTCGAACTACTGGCTTCAAGCAATCCTC A G PVT1 Ensembl:ENSG00000249859 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs763019928 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75888,RMVar_hsa_circ_118838,RMVar_hsa_circ_101526,RMVar_hsa_circ_254319,RMVar_hsa_circ_254320,RMVar_hsa_circ_107291,RMVar_hsa_circ_254322,RMVar_hsa_circ_369306,RMVar_hsa_circ_111912,RMVar_hsa_circ_115647,RMVar_hsa_circ_254324,RMVar_hsa_circ_254325,RMVar_hsa_circ_371319,RMVar_hsa_circ_373231,RMVar_hsa_circ_254323,RMVar_hsa_circ_296671,RMVar_hsa_circ_254330,RMVar_hsa_circ_254332,RMVar_hsa_circ_254333,RMVar_hsa_circ_254331 16202 RMVar_ID_16202 Human_SNP_ID_381878064 A-to-I Human chr8 + 127978666 127978666 127978666 CCACCACACCTGGCTAATTTTTTTGTGGTTTTAGTAGAGATGAGGTTTCACCATATTGTCCAGGC CCACCACACCTGGCTAATTTTTTTGTGGTTTTTGTAGAGATGAGGTTTCACCATATTGTCCAGGC A T PVT1 Ensembl:ENSG00000249859 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs571994268 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75888,RMVar_hsa_circ_118838,RMVar_hsa_circ_101526,RMVar_hsa_circ_254319,RMVar_hsa_circ_254320,RMVar_hsa_circ_107291,RMVar_hsa_circ_254322,RMVar_hsa_circ_369306,RMVar_hsa_circ_111912,RMVar_hsa_circ_115647,RMVar_hsa_circ_254324,RMVar_hsa_circ_254325,RMVar_hsa_circ_371319,RMVar_hsa_circ_373231,RMVar_hsa_circ_254323,RMVar_hsa_circ_296671,RMVar_hsa_circ_254330,RMVar_hsa_circ_254332,RMVar_hsa_circ_254333,RMVar_hsa_circ_254331 16203 RMVar_ID_16203 Human_SNP_ID_381878067 A-to-I Human chr8 + 127978683 127978683 127978683 TTTTTTTGTGGTTTTAGTAGAGATGAGGTTTCACCATATTGTCCAGGCTGGTCTAGAACTCGTGA TTTTTTTGTGGTTTTAGTAGAGATGAGGTTTCGCCATATTGTCCAGGCTGGTCTAGAACTCGTGA A G PVT1 Ensembl:ENSG00000249859 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1292010901 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16357232 RMVar_hsa_circ_75888,RMVar_hsa_circ_118838,RMVar_hsa_circ_101526,RMVar_hsa_circ_254319,RMVar_hsa_circ_254320,RMVar_hsa_circ_107291,RMVar_hsa_circ_254322,RMVar_hsa_circ_369306,RMVar_hsa_circ_111912,RMVar_hsa_circ_115647,RMVar_hsa_circ_254324,RMVar_hsa_circ_254325,RMVar_hsa_circ_371319,RMVar_hsa_circ_373231,RMVar_hsa_circ_254323,RMVar_hsa_circ_296671,RMVar_hsa_circ_254330,RMVar_hsa_circ_254332,RMVar_hsa_circ_254333,RMVar_hsa_circ_254331 16204 RMVar_ID_16204 Human_SNP_ID_381878068 A-to-I Human chr8 + 127978686 127978686 127978686 TTTTGTGGTTTTAGTAGAGATGAGGTTTCACCATATTGTCCAGGCTGGTCTAGAACTCGTGAAAA TTTTGTGGTTTTAGTAGAGATGAGGTTTCACCGTATTGTCCAGGCTGGTCTAGAACTCGTGAAAA A G PVT1 Ensembl:ENSG00000249859 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978239530 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16357232 RMVar_hsa_circ_75888,RMVar_hsa_circ_118838,RMVar_hsa_circ_101526,RMVar_hsa_circ_254319,RMVar_hsa_circ_254320,RMVar_hsa_circ_107291,RMVar_hsa_circ_254322,RMVar_hsa_circ_369306,RMVar_hsa_circ_111912,RMVar_hsa_circ_115647,RMVar_hsa_circ_254324,RMVar_hsa_circ_254325,RMVar_hsa_circ_371319,RMVar_hsa_circ_373231,RMVar_hsa_circ_254323,RMVar_hsa_circ_296671,RMVar_hsa_circ_254330,RMVar_hsa_circ_254332,RMVar_hsa_circ_254333,RMVar_hsa_circ_254331 16205 RMVar_ID_16205 Human_SNP_ID_381884795 A-to-I Human chr8 + 128003430 128003430 128003430 TACAGTGGAAGGATCATGGCCCACTGTAGCCTAGACATCCCAGGCTGAAATGATCCTCTCTCCTC TACAGTGGAAGGATCATGGCCCACTGTAGCCTCGACATCCCAGGCTGAAATGATCCTCTCTCCTC A C PVT1 Ensembl:ENSG00000249859 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1451108412 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1223646,Human_RBP_ID_5106002,Human_RBP_ID_16358042 RMVar_hsa_circ_75888,RMVar_hsa_circ_118838,RMVar_hsa_circ_254320,RMVar_hsa_circ_125092,RMVar_hsa_circ_107291,RMVar_hsa_circ_254322,RMVar_hsa_circ_115647,RMVar_hsa_circ_371319,RMVar_hsa_circ_373231,RMVar_hsa_circ_254323,RMVar_hsa_circ_254332,RMVar_hsa_circ_254333,RMVar_hsa_circ_254331,RMVar_hsa_circ_76237,RMVar_hsa_circ_254334,RMVar_hsa_circ_254335,RMVar_hsa_circ_77631,RMVar_hsa_circ_338304,RMVar_hsa_circ_19203,RMVar_hsa_circ_254337,RMVar_hsa_circ_254338,RMVar_hsa_circ_254339 16206 RMVar_ID_16206 Human_SNP_ID_381887720 A-to-I Human chr8 + 128015728 128015728 128015728 CTGGGAGGCGGAGGTTGCAGTGAGCCAAGATCACGCCACTGCACTCCAGCCTGGTGACTGAGCAA CTGGGAGGCGGAGGTTGCAGTGAGCCAAGATCGCGCCACTGCACTCCAGCCTGGTGACTGAGCAA A G PVT1 Ensembl:ENSG00000249859 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232450198 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10385665,Human_RBP_ID_16358468,Human_RBP_ID_26152869 RMVar_hsa_circ_75888,RMVar_hsa_circ_118838,RMVar_hsa_circ_254320,RMVar_hsa_circ_125092,RMVar_hsa_circ_107291,RMVar_hsa_circ_254322,RMVar_hsa_circ_115647,RMVar_hsa_circ_371319,RMVar_hsa_circ_373231,RMVar_hsa_circ_254323,RMVar_hsa_circ_254332,RMVar_hsa_circ_254333,RMVar_hsa_circ_254331,RMVar_hsa_circ_76237,RMVar_hsa_circ_254334,RMVar_hsa_circ_254335,RMVar_hsa_circ_77631,RMVar_hsa_circ_338304,RMVar_hsa_circ_254338,RMVar_hsa_circ_254339,RMVar_hsa_circ_301347,RMVar_hsa_circ_309118,RMVar_hsa_circ_80977,RMVar_hsa_circ_254341 16207 RMVar_ID_16207 Human_SNP_ID_381887833 A-to-I Human chr8 + 128016171 128016171 128016171 GTGGTGGCACATGCCTGTGGTCTCAGCTACTTAAGAGACTGAATAGGAGGATCACCAGAATCTGG GTGGTGGCACATGCCTGTGGTCTCAGCTACTTGAGAGACTGAATAGGAGGATCACCAGAATCTGG A G PVT1 Ensembl:ENSG00000249859 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909949038 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3141299 RMVar_hsa_circ_75888,RMVar_hsa_circ_118838,RMVar_hsa_circ_254320,RMVar_hsa_circ_125092,RMVar_hsa_circ_107291,RMVar_hsa_circ_254322,RMVar_hsa_circ_115647,RMVar_hsa_circ_371319,RMVar_hsa_circ_373231,RMVar_hsa_circ_254323,RMVar_hsa_circ_254332,RMVar_hsa_circ_254333,RMVar_hsa_circ_254331,RMVar_hsa_circ_76237,RMVar_hsa_circ_254334,RMVar_hsa_circ_254335,RMVar_hsa_circ_77631,RMVar_hsa_circ_338304,RMVar_hsa_circ_254338,RMVar_hsa_circ_254339,RMVar_hsa_circ_301347,RMVar_hsa_circ_309118,RMVar_hsa_circ_80977,RMVar_hsa_circ_254341 16208 RMVar_ID_16208 Human_SNP_ID_381887837 A-to-I Human chr8 + 128016195 128016195 128016195 AGCTACTTAAGAGACTGAATAGGAGGATCACCAGAATCTGGGAGGTGGAGATTGCGGTGAACCAA AGCTACTTAAGAGACTGAATAGGAGGATCACCGGAATCTGGGAGGTGGAGATTGCGGTGAACCAA A G PVT1 Ensembl:ENSG00000249859 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs781327343 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5106803 RMVar_hsa_circ_75888,RMVar_hsa_circ_118838,RMVar_hsa_circ_254320,RMVar_hsa_circ_125092,RMVar_hsa_circ_107291,RMVar_hsa_circ_254322,RMVar_hsa_circ_115647,RMVar_hsa_circ_371319,RMVar_hsa_circ_373231,RMVar_hsa_circ_254323,RMVar_hsa_circ_254332,RMVar_hsa_circ_254333,RMVar_hsa_circ_254331,RMVar_hsa_circ_76237,RMVar_hsa_circ_254334,RMVar_hsa_circ_254335,RMVar_hsa_circ_77631,RMVar_hsa_circ_338304,RMVar_hsa_circ_254338,RMVar_hsa_circ_254339,RMVar_hsa_circ_301347,RMVar_hsa_circ_309118,RMVar_hsa_circ_80977,RMVar_hsa_circ_254341 16209 RMVar_ID_16209 Human_SNP_ID_381888035 A-to-I Human chr8 + 128016957 128016957 128016957 CCTGTAATCCCAGCACTTCGGGAGGCCAAGGTAAGAGTATGGCTTGAGCCCAGGAGTTCAAGGCA CCTGTAATCCCAGCACTTCGGGAGGCCAAGGTTAGAGTATGGCTTGAGCCCAGGAGTTCAAGGCA A T PVT1 Ensembl:ENSG00000249859 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1250023198 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2039764 RMVar_hsa_circ_75888,RMVar_hsa_circ_118838,RMVar_hsa_circ_254320,RMVar_hsa_circ_125092,RMVar_hsa_circ_107291,RMVar_hsa_circ_254322,RMVar_hsa_circ_115647,RMVar_hsa_circ_371319,RMVar_hsa_circ_373231,RMVar_hsa_circ_254323,RMVar_hsa_circ_254332,RMVar_hsa_circ_254333,RMVar_hsa_circ_254331,RMVar_hsa_circ_76237,RMVar_hsa_circ_254334,RMVar_hsa_circ_254335,RMVar_hsa_circ_77631,RMVar_hsa_circ_338304,RMVar_hsa_circ_254338,RMVar_hsa_circ_254339,RMVar_hsa_circ_301347,RMVar_hsa_circ_309118,RMVar_hsa_circ_80977,RMVar_hsa_circ_254341 16210 RMVar_ID_16210 Human_SNP_ID_381888181 A-to-I Human chr8 + 128017657 128017657 128017657 AGGGATCTTGCTATGTTGCCAGGGCTGGTCTCAAACTCCTGGGCTCAAGTTATCCTCCTGCCTCG AGGGATCTTGCTATGTTGCCAGGGCTGGTCTCCAACTCCTGGGCTCAAGTTATCCTCCTGCCTCG A C PVT1 Ensembl:ENSG00000249859 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1420885537 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22625565 RMVar_hsa_circ_75888,RMVar_hsa_circ_118838,RMVar_hsa_circ_254320,RMVar_hsa_circ_125092,RMVar_hsa_circ_107291,RMVar_hsa_circ_254322,RMVar_hsa_circ_115647,RMVar_hsa_circ_371319,RMVar_hsa_circ_373231,RMVar_hsa_circ_254323,RMVar_hsa_circ_254332,RMVar_hsa_circ_254333,RMVar_hsa_circ_254331,RMVar_hsa_circ_76237,RMVar_hsa_circ_254334,RMVar_hsa_circ_254335,RMVar_hsa_circ_77631,RMVar_hsa_circ_338304,RMVar_hsa_circ_254338,RMVar_hsa_circ_254339,RMVar_hsa_circ_301347,RMVar_hsa_circ_309118,RMVar_hsa_circ_80977,RMVar_hsa_circ_254341 16211 RMVar_ID_16211 Human_SNP_ID_381891106 A-to-I Human chr8 + 128029538 128029538 128029538 AAAATACTTGTTGCGGTCGGGTGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAG AAAATACTTGTTGCGGTCGGGTGCGGTGGCTCCCGCCTGTAATCCCAGCACTTTGGGAGGCCGAG A C PVT1 Ensembl:ENSG00000249859 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1019647867 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75888,RMVar_hsa_circ_118838,RMVar_hsa_circ_254320,RMVar_hsa_circ_125092,RMVar_hsa_circ_107291,RMVar_hsa_circ_254322,RMVar_hsa_circ_115647,RMVar_hsa_circ_371319,RMVar_hsa_circ_373231,RMVar_hsa_circ_254323,RMVar_hsa_circ_254332,RMVar_hsa_circ_254333,RMVar_hsa_circ_254331,RMVar_hsa_circ_76237,RMVar_hsa_circ_254334,RMVar_hsa_circ_254335,RMVar_hsa_circ_77631,RMVar_hsa_circ_338304,RMVar_hsa_circ_254338,RMVar_hsa_circ_254339,RMVar_hsa_circ_301347,RMVar_hsa_circ_309118 16212 RMVar_ID_16212 Human_SNP_ID_381891107 A-to-I Human chr8 + 128029538 128029538 128029538 AAAATACTTGTTGCGGTCGGGTGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAG AAAATACTTGTTGCGGTCGGGTGCGGTGGCTCTCGCCTGTAATCCCAGCACTTTGGGAGGCCGAG A T PVT1 Ensembl:ENSG00000249859 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1019647867 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75888,RMVar_hsa_circ_118838,RMVar_hsa_circ_254320,RMVar_hsa_circ_125092,RMVar_hsa_circ_107291,RMVar_hsa_circ_254322,RMVar_hsa_circ_115647,RMVar_hsa_circ_371319,RMVar_hsa_circ_373231,RMVar_hsa_circ_254323,RMVar_hsa_circ_254332,RMVar_hsa_circ_254333,RMVar_hsa_circ_254331,RMVar_hsa_circ_76237,RMVar_hsa_circ_254334,RMVar_hsa_circ_254335,RMVar_hsa_circ_77631,RMVar_hsa_circ_338304,RMVar_hsa_circ_254338,RMVar_hsa_circ_254339,RMVar_hsa_circ_301347,RMVar_hsa_circ_309118 16213 RMVar_ID_16213 Human_SNP_ID_381902899 A-to-I Human chr8 + 128078885 128078885 128078885 ATGGCTCACTGCAGCCTCGACGTCCTGGGCTCAAGCAATTCTCCCACCTCAGCACCCCCCGAGTA ATGGCTCACTGCAGCCTCGACGTCCTGGGCTCCAGCAATTCTCCCACCTCAGCACCCCCCGAGTA A C PVT1 Ensembl:ENSG00000249859 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1043989036 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16360050 RMVar_hsa_circ_107291,RMVar_hsa_circ_373231,RMVar_hsa_circ_254332,RMVar_hsa_circ_254333,RMVar_hsa_circ_76237,RMVar_hsa_circ_254334,RMVar_hsa_circ_338304,RMVar_hsa_circ_254339,RMVar_hsa_circ_309118,RMVar_hsa_circ_106386,RMVar_hsa_circ_371304,RMVar_hsa_circ_254343,RMVar_hsa_circ_254344 16214 RMVar_ID_16214 Human_SNP_ID_381906300 A-to-I Human chr8 + 128093699 128093698 128093699 TAGCTCTGTCACCCAGGCTGGAGCGCTACAGCACAGTCTCGGCTCACTGCAACCTCCGCCTCCCA TAGCTCTGTCACCCAGGCTGGAGCGCTACAGC_CAGTCTCGGCTCACTGCAACCTCCGCCTCCCA CA C PVT1 Ensembl:ENSG00000249859 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1328555873 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_107291,RMVar_hsa_circ_373231,RMVar_hsa_circ_254332,RMVar_hsa_circ_254333,RMVar_hsa_circ_76237,RMVar_hsa_circ_254334,RMVar_hsa_circ_338304,RMVar_hsa_circ_254339,RMVar_hsa_circ_106386,RMVar_hsa_circ_371304,RMVar_hsa_circ_254343,RMVar_hsa_circ_254344 16215 RMVar_ID_16215 Human_SNP_ID_382353688 A-to-I Human chr8 - 129847207 129847207 129847207 CGCCCGCCTCAGCCTCCCAAAGTGTTGGAATTACAGGCCTGAGCCACCCTGCCCAGCCCATTCTG CGCCCGCCTCAGCCTCCCAAAGTGTTGGAATTGCAGGCCTGAGCCACCCTGCCCAGCCCATTCTG T C CYRIB Ensembl:ENSG00000153310 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1454207424 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58921,RMVar_hsa_circ_349114,RMVar_hsa_circ_93382,RMVar_hsa_circ_254347,RMVar_hsa_circ_359141,RMVar_hsa_circ_274343,RMVar_hsa_circ_320983,RMVar_hsa_circ_101693,RMVar_hsa_circ_254348,RMVar_hsa_circ_21312,RMVar_hsa_circ_57269,RMVar_hsa_circ_254349,RMVar_hsa_circ_254350 16216 RMVar_ID_16216 Human_SNP_ID_382353690 A-to-I Human chr8 - 129847219 129847218 129847220 GACCTTGTGATCCGCCCGCCTCAGCCTCCCAAAGTGTTGGAATTACAGGCCTGAGCCACCCTGCC GACCTTGTGATCCGCCCGCCTCAGCCTCCCA__GTGTTGGAATTACAGGCCTGAGCCACCCTGCC CTT C CYRIB Ensembl:ENSG00000153310 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1346782020 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_58921,RMVar_hsa_circ_349114,RMVar_hsa_circ_93382,RMVar_hsa_circ_254347,RMVar_hsa_circ_359141,RMVar_hsa_circ_274343,RMVar_hsa_circ_320983,RMVar_hsa_circ_101693,RMVar_hsa_circ_254348,RMVar_hsa_circ_21312,RMVar_hsa_circ_57269,RMVar_hsa_circ_254349,RMVar_hsa_circ_254350 16217 RMVar_ID_16217 Human_SNP_ID_382353693 A-to-I Human chr8 - 129847229 129847229 129847229 TCGAACTCCTGACCTTGTGATCCGCCCGCCTCAGCCTCCCAAAGTGTTGGAATTACAGGCCTGAG TCGAACTCCTGACCTTGTGATCCGCCCGCCTCGGCCTCCCAAAGTGTTGGAATTACAGGCCTGAG T C CYRIB Ensembl:ENSG00000153310 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs927577622 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58921,RMVar_hsa_circ_349114,RMVar_hsa_circ_93382,RMVar_hsa_circ_254347,RMVar_hsa_circ_359141,RMVar_hsa_circ_274343,RMVar_hsa_circ_320983,RMVar_hsa_circ_101693,RMVar_hsa_circ_254348,RMVar_hsa_circ_21312,RMVar_hsa_circ_57269,RMVar_hsa_circ_254349,RMVar_hsa_circ_254350 16218 RMVar_ID_16218 Human_SNP_ID_382363892 A-to-I Human chr8 - 129889898 129889898 129889898 GTGATGGCTTGTGCCTGTAGTCTCAGCTACTCAGTAGGTTGAGGCACGAGAATTGCTTGAACCCG GTGATGGCTTGTGCCTGTAGTCTCAGCTACTCGGTAGGTTGAGGCACGAGAATTGCTTGAACCCG T C CYRIB Ensembl:ENSG00000153310 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1189554648 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 16219 RMVar_ID_16219 Human_SNP_ID_382363895 A-to-I Human chr8 - 129889902 129889902 129889902 GGCTGTGATGGCTTGTGCCTGTAGTCTCAGCTACTCAGTAGGTTGAGGCACGAGAATTGCTTGAA GGCTGTGATGGCTTGTGCCTGTAGTCTCAGCTGCTCAGTAGGTTGAGGCACGAGAATTGCTTGAA T C CYRIB Ensembl:ENSG00000153310 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1366352235 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 16220 RMVar_ID_16220 Human_SNP_ID_382363897 A-to-I Human chr8 - 129889912 129889912 129889912 AAAATCAGCTGGCTGTGATGGCTTGTGCCTGTAGTCTCAGCTACTCAGTAGGTTGAGGCACGAGA AAAATCAGCTGGCTGTGATGGCTTGTGCCTGTTGTCTCAGCTACTCAGTAGGTTGAGGCACGAGA T A CYRIB Ensembl:ENSG00000153310 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs957781377 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 16221 RMVar_ID_16221 Human_SNP_ID_382363903 A-to-I Human chr8 - 129889938 129889938 129889938 GAAACCCTATCTCTACTAAAATACAAAAAATCAGCTGGCTGTGATGGCTTGTGCCTGTAGTCTCA GAAACCCTATCTCTACTAAAATACAAAAAATCGGCTGGCTGTGATGGCTTGTGCCTGTAGTCTCA T C CYRIB Ensembl:ENSG00000153310 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1564689435 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 16222 RMVar_ID_16222 Human_SNP_ID_382368856 A-to-I Human chr8 - 129910931 129910931 129910931 GAGAGAGGCCGGGCAAGGTGGCTCATGCCTATAATTCCAGCGCTTTTGGAGGCCAAGGAGGGAGA GAGAGAGGCCGGGCAAGGTGGCTCATGCCTATGATTCCAGCGCTTTTGGAGGCCAAGGAGGGAGA T C CYRIB Ensembl:ENSG00000153310 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1276909115 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25988,RMVar_hsa_circ_306774,RMVar_hsa_circ_335333,RMVar_hsa_circ_284834,RMVar_hsa_circ_107686,RMVar_hsa_circ_254368 16223 RMVar_ID_16223 Human_SNP_ID_382371823 A-to-I Human chr8 - 129923412 129923412 129923412 AAATTAGCTGGGTGTGGTGGCGAGCGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGAACGAGAA AAATTAGCTGGGTGTGGTGGCGAGCGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGAACGAGAA T C CYRIB Ensembl:ENSG00000153310 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1163460905 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_306774,RMVar_hsa_circ_335333 16224 RMVar_ID_16224 Human_SNP_ID_382378333 A-to-I Human chr8 - 129948842 129948842 129948842 CAGGCTGGTCTCAAGCAATTCTGGGCTCAAGCAGTCCTCCCACCTTGGCCTCCCAAAGTGCTGGG CAGGCTGGTCTCAAGCAATTCTGGGCTCAAGCTGTCCTCCCACCTTGGCCTCCCAAAGTGCTGGG T A CYRIB Ensembl:ENSG00000153310 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1478229699 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_306774,RMVar_hsa_circ_335333 16225 RMVar_ID_16225 Human_SNP_ID_382378383 A-to-I Human chr8 - 129949036 129949036 129949036 GGGTCCCACCCTGTCGCCCAGGCCAGAGTGCAATAGTGCAATCACGACCCACTGCATCCTTGACC GGGTCCCACCCTGTCGCCCAGGCCAGAGTGCAGTAGTGCAATCACGACCCACTGCATCCTTGACC T C CYRIB Ensembl:ENSG00000153310 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1309228396 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1011378,Human_Splice_Rec_1011379 RMVar_hsa_circ_306774,RMVar_hsa_circ_335333 16226 RMVar_ID_16226 Human_SNP_ID_382378384 A-to-I Human chr8 - 129949036 129949036 129949036 GGGTCCCACCCTGTCGCCCAGGCCAGAGTGCAATAGTGCAATCACGACCCACTGCATCCTTGACC GGGTCCCACCCTGTCGCCCAGGCCAGAGTGCACTAGTGCAATCACGACCCACTGCATCCTTGACC T G CYRIB Ensembl:ENSG00000153310 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1309228396 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1011378,Human_Splice_Rec_1011379 RMVar_hsa_circ_306774,RMVar_hsa_circ_335333 16227 RMVar_ID_16227 Human_SNP_ID_382382224 A-to-I Human chr8 - 129965955 129965955 129965955 CCCAGTTACTCGGGAAGCCGACGTAGGAGAATAGCTTGAATCTGGGAGGCGGAGGCTGCAGTGAG CCCAGTTACTCGGGAAGCCGACGTAGGAGAATGGCTTGAATCTGGGAGGCGGAGGCTGCAGTGAG T C CYRIB Ensembl:ENSG00000153310 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1401982565 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_335333 16228 RMVar_ID_16228 Human_SNP_ID_382382244 A-to-I Human chr8 - 129966039 129966039 129966039 AGCCTGACCAACATGGTAGAAACTGTGTCTCTACCAAAAAATACAAAAATTAGCTGGGTGTTGTG AGCCTGACCAACATGGTAGAAACTGTGTCTCTGCCAAAAAATACAAAAATTAGCTGGGTGTTGTG T C CYRIB Ensembl:ENSG00000153310 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1564471903 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_335333 16229 RMVar_ID_16229 Human_SNP_ID_382391150 A-to-I Human chr8 - 130002349 130002349 130002349 TCAGGTGATCCTCCTGCCTCAGCGTCCCGAGCAGCTGGGACCACAGGTGCATGCCACTACATCTG TCAGGTGATCCTCCTGCCTCAGCGTCCCGAGCCGCTGGGACCACAGGTGCATGCCACTACATCTG T G CYRIB Ensembl:ENSG00000153310 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs905297638 Functional Loss SNV dbSNP153 33..33 33 - - - 16230 RMVar_ID_16230 Human_SNP_ID_382391159 A-to-I Human chr8 - 130002379 130002379 130002379 ACAGCTCACTGCAGCCTCGACCTCTCTGGCTCAGGTGATCCTCCTGCCTCAGCGTCCCGAGCAGC ACAGCTCACTGCAGCCTCGACCTCTCTGGCTCGGGTGATCCTCCTGCCTCAGCGTCCCGAGCAGC T C CYRIB Ensembl:ENSG00000153310 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs948727912 Functional Loss SNV dbSNP153 33..33 33 - - - 16231 RMVar_ID_16231 Human_SNP_ID_382391160 A-to-I Human chr8 - 130002379 130002379 130002379 ACAGCTCACTGCAGCCTCGACCTCTCTGGCTCAGGTGATCCTCCTGCCTCAGCGTCCCGAGCAGC ACAGCTCACTGCAGCCTCGACCTCTCTGGCTCCGGTGATCCTCCTGCCTCAGCGTCCCGAGCAGC T G CYRIB Ensembl:ENSG00000153310 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs948727912 Functional Loss SNV dbSNP153 33..33 33 - - - 16232 RMVar_ID_16232 Human_SNP_ID_382391320 A-to-I Human chr8 - 130003136 130003136 130003136 ATGATGCAGCCTTGACCTCCAGGGTTCAAGCAATCCTCCCACCTCAGCCTCCCGAGTACCTCAGT ATGATGCAGCCTTGACCTCCAGGGTTCAAGCAGTCCTCCCACCTCAGCCTCCCGAGTACCTCAGT T C CYRIB Ensembl:ENSG00000153310 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs532687082 Functional Loss SNV dbSNP153 33..33 33 - - - 16233 RMVar_ID_16233 Human_SNP_ID_382392756 A-to-I Human chr8 - 130008043 130008043 130008043 AACCATACCTGGCTAATTTTTGTACTTTTAGTAGAGATGGAGTTTCACCATGTTGGACAGGCCAG AACCATACCTGGCTAATTTTTGTACTTTTAGTGGAGATGGAGTTTCACCATGTTGGACAGGCCAG T C CYRIB Ensembl:ENSG00000153310 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs922221807 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16362512 16234 RMVar_ID_16234 Human_SNP_ID_382412064 A-to-I Human chr8 - 130078410 130078410 130078410 TGGTGGTACATACCTGGCTATACGGGAGGCTGAGGCAAGAGGACCGCCTGAGCCCAGGAAATTGA TGGTGGTACATACCTGGCTATACGGGAGGCTGGGGCAAGAGGACCGCCTGAGCCCAGGAAATTGA T C ASAP1 Ensembl:ENSG00000153317 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1002191674 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16362663 RMVar_hsa_circ_8573,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_254372,RMVar_hsa_circ_323019,RMVar_hsa_circ_342441,RMVar_hsa_circ_254371,RMVar_hsa_circ_374776,RMVar_hsa_circ_323361,RMVar_hsa_circ_96424,RMVar_hsa_circ_99240,RMVar_hsa_circ_254374,RMVar_hsa_circ_254375,RMVar_hsa_circ_254373 16235 RMVar_ID_16235 Human_SNP_ID_382415601 A-to-I Human chr8 - 130092532 130092532 130092532 TCCTCGAACTCCTGACTTCAAGTGATCCTCCTACCTCAGTCTTCCAAGTAGCTGAGACTACAAGC TCCTCGAACTCCTGACTTCAAGTGATCCTCCTGCCTCAGTCTTCCAAGTAGCTGAGACTACAAGC T C ASAP1 Ensembl:ENSG00000153317 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1231058338 Functional Loss SNV dbSNP153 33..33 33 - - - 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_254379 16236 RMVar_ID_16236 Human_SNP_ID_382481881 A-to-I Human chr8 - 130354961 130354961 130354961 GAATCATATGAACCCGGGAGGCCGAGGTTACAATGAGCCAAGATCGCACCACTGCACACCAGGTT GAATCATATGAACCCGGGAGGCCGAGGTTACAGTGAGCCAAGATCGCACCACTGCACACCAGGTT T C ASAP1 Ensembl:ENSG00000153317 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1001625373 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_87937,RMVar_hsa_circ_119862,RMVar_hsa_circ_35465,RMVar_hsa_circ_254410,RMVar_hsa_circ_254409,RMVar_hsa_circ_283052,RMVar_hsa_circ_306382,RMVar_hsa_circ_254422,RMVar_hsa_circ_254423,RMVar_hsa_circ_295523,RMVar_hsa_circ_254431,RMVar_hsa_circ_87768,RMVar_hsa_circ_336221,RMVar_hsa_circ_254433,RMVar_hsa_circ_31200,RMVar_hsa_circ_254443,RMVar_hsa_circ_254437,RMVar_hsa_circ_351942,RMVar_hsa_circ_375255,RMVar_hsa_circ_254438,RMVar_hsa_circ_277578,RMVar_hsa_circ_288860,RMVar_hsa_circ_312193,RMVar_hsa_circ_254441,RMVar_hsa_circ_254442,RMVar_hsa_circ_77337,RMVar_hsa_circ_254445,RMVar_hsa_circ_316777,RMVar_hsa_circ_328571,RMVar_hsa_circ_306600,RMVar_hsa_circ_254444,RMVar_hsa_circ_76417,RMVar_hsa_circ_254447,RMVar_hsa_circ_254448,RMVar_hsa_circ_254450 16237 RMVar_ID_16237 Human_SNP_ID_382490769 A-to-I Human chr8 - 130390528 130390528 130390528 AGTATGTCAGGGGAAATAGATATCTAACAGGTAATTTCAGTCCAGTATGGTAGGTGTAATCATAT AGTATGTCAGGGGAAATAGATATCTAACAGGTCATTTCAGTCCAGTATGGTAGGTGTAATCATAT T G ASAP1 Ensembl:ENSG00000153317 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1257494997 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92693,RMVar_hsa_circ_254384,RMVar_hsa_circ_122496,RMVar_hsa_circ_254399,RMVar_hsa_circ_87937,RMVar_hsa_circ_35465,RMVar_hsa_circ_254409,RMVar_hsa_circ_111342,RMVar_hsa_circ_254443,RMVar_hsa_circ_375255,RMVar_hsa_circ_254438,RMVar_hsa_circ_312193,RMVar_hsa_circ_306600,RMVar_hsa_circ_275064,RMVar_hsa_circ_116691,RMVar_hsa_circ_254454,RMVar_hsa_circ_101120,RMVar_hsa_circ_105920,RMVar_hsa_circ_254455,RMVar_hsa_circ_254452,RMVar_hsa_circ_254453,RMVar_hsa_circ_254451,RMVar_hsa_circ_51629 16238 RMVar_ID_16238 Human_SNP_ID_382490770 A-to-I Human chr8 - 130390532 130390531 130390532 TCAGAGTATGTCAGGGGAAATAGATATCTAACAGGTAATTTCAGTCCAGTATGGTAGGTGTAATC TCAGAGTATGTCAGGGGAAATAGATATCTAAC_GGTAATTTCAGTCCAGTATGGTAGGTGTAATC CT C ASAP1 Ensembl:ENSG00000153317 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1160213063 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_92693,RMVar_hsa_circ_254384,RMVar_hsa_circ_122496,RMVar_hsa_circ_254399,RMVar_hsa_circ_87937,RMVar_hsa_circ_35465,RMVar_hsa_circ_254409,RMVar_hsa_circ_111342,RMVar_hsa_circ_254443,RMVar_hsa_circ_375255,RMVar_hsa_circ_254438,RMVar_hsa_circ_312193,RMVar_hsa_circ_306600,RMVar_hsa_circ_275064,RMVar_hsa_circ_116691,RMVar_hsa_circ_254454,RMVar_hsa_circ_101120,RMVar_hsa_circ_105920,RMVar_hsa_circ_254455,RMVar_hsa_circ_254452,RMVar_hsa_circ_254453,RMVar_hsa_circ_254451,RMVar_hsa_circ_51629 16239 RMVar_ID_16239 Human_SNP_ID_382491087 A-to-I Human chr8 - 130391715 130391715 130391715 TGTATTGGACTGAAATGACCTGTTAGATATCTATTGCCACTGACATACTCTGAGTGCCTTGAAGG TGTATTGGACTGAAATGACCTGTTAGATATCTGTTGCCACTGACATACTCTGAGTGCCTTGAAGG T C ASAP1 Ensembl:ENSG00000153317 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs528885776 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92693,RMVar_hsa_circ_254384,RMVar_hsa_circ_122496,RMVar_hsa_circ_254399,RMVar_hsa_circ_87937,RMVar_hsa_circ_35465,RMVar_hsa_circ_254409,RMVar_hsa_circ_111342,RMVar_hsa_circ_254443,RMVar_hsa_circ_375255,RMVar_hsa_circ_254438,RMVar_hsa_circ_312193,RMVar_hsa_circ_306600,RMVar_hsa_circ_275064,RMVar_hsa_circ_116691,RMVar_hsa_circ_254454,RMVar_hsa_circ_101120,RMVar_hsa_circ_105920,RMVar_hsa_circ_254455,RMVar_hsa_circ_254452,RMVar_hsa_circ_254453,RMVar_hsa_circ_254451,RMVar_hsa_circ_51629 16240 RMVar_ID_16240 Human_SNP_ID_382491089 A-to-I Human chr8 - 130391733 130391733 130391733 ATACATTATTACATTTACTGTATTGGACTGAAATGACCTGTTAGATATCTATTGCCACTGACATA ATACATTATTACATTTACTGTATTGGACTGAATTGACCTGTTAGATATCTATTGCCACTGACATA T A ASAP1 Ensembl:ENSG00000153317 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs892543912 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92693,RMVar_hsa_circ_254384,RMVar_hsa_circ_122496,RMVar_hsa_circ_254399,RMVar_hsa_circ_87937,RMVar_hsa_circ_35465,RMVar_hsa_circ_254409,RMVar_hsa_circ_111342,RMVar_hsa_circ_254443,RMVar_hsa_circ_375255,RMVar_hsa_circ_254438,RMVar_hsa_circ_312193,RMVar_hsa_circ_306600,RMVar_hsa_circ_275064,RMVar_hsa_circ_116691,RMVar_hsa_circ_254454,RMVar_hsa_circ_101120,RMVar_hsa_circ_105920,RMVar_hsa_circ_254455,RMVar_hsa_circ_254452,RMVar_hsa_circ_254453,RMVar_hsa_circ_254451,RMVar_hsa_circ_51629 16241 RMVar_ID_16241 Human_SNP_ID_382491099 A-to-I Human chr8 - 130391765 130391765 130391765 CTCTCTAAAAAGGTATAATGTGCTATCTAAGAATACATTATTACATTTACTGTATTGGACTGAAA CTCTCTAAAAAGGTATAATGTGCTATCTAAGAGTACATTATTACATTTACTGTATTGGACTGAAA T C ASAP1 Ensembl:ENSG00000153317 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1384047351 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92693,RMVar_hsa_circ_254384,RMVar_hsa_circ_122496,RMVar_hsa_circ_254399,RMVar_hsa_circ_87937,RMVar_hsa_circ_35465,RMVar_hsa_circ_254409,RMVar_hsa_circ_111342,RMVar_hsa_circ_254443,RMVar_hsa_circ_375255,RMVar_hsa_circ_254438,RMVar_hsa_circ_312193,RMVar_hsa_circ_306600,RMVar_hsa_circ_275064,RMVar_hsa_circ_116691,RMVar_hsa_circ_254454,RMVar_hsa_circ_101120,RMVar_hsa_circ_105920,RMVar_hsa_circ_254455,RMVar_hsa_circ_254452,RMVar_hsa_circ_254453,RMVar_hsa_circ_254451,RMVar_hsa_circ_51629 16242 RMVar_ID_16242 Human_SNP_ID_382491101 A-to-I Human chr8 - 130391768 130391767 130391768 GCTCTCTCTAAAAAGGTATAATGTGCTATCTAAGAATACATTATTACATTTACTGTATTGGACTG GCTCTCTCTAAAAAGGTATAATGTGCTATCTA_GAATACATTATTACATTTACTGTATTGGACTG CT C ASAP1 Ensembl:ENSG00000153317 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1395113419 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_92693,RMVar_hsa_circ_254384,RMVar_hsa_circ_122496,RMVar_hsa_circ_254399,RMVar_hsa_circ_87937,RMVar_hsa_circ_35465,RMVar_hsa_circ_254409,RMVar_hsa_circ_111342,RMVar_hsa_circ_254443,RMVar_hsa_circ_375255,RMVar_hsa_circ_254438,RMVar_hsa_circ_312193,RMVar_hsa_circ_306600,RMVar_hsa_circ_275064,RMVar_hsa_circ_116691,RMVar_hsa_circ_254454,RMVar_hsa_circ_101120,RMVar_hsa_circ_105920,RMVar_hsa_circ_254455,RMVar_hsa_circ_254452,RMVar_hsa_circ_254453,RMVar_hsa_circ_254451,RMVar_hsa_circ_51629 16243 RMVar_ID_16243 Human_SNP_ID_382502158 A-to-I Human chr8 - 130436460 130436460 130436460 CCAAAAATAACAAAAAACAAATAACAAAAATTAGCCAGACATGGTGGTGCACTCCTGTAGTCCCA CCAAAAATAACAAAAAACAAATAACAAAAATTGGCCAGACATGGTGGTGCACTCCTGTAGTCCCA T C ASAP1 Ensembl:ENSG00000153317 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348236697 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116691,RMVar_hsa_circ_254451,RMVar_hsa_circ_254460,RMVar_hsa_circ_90905 16244 RMVar_ID_16244 Human_SNP_ID_382954491 A-to-I Human chr8 - 132122315 132122315 132122315 AAAAGTGAGGTCAGGGAAGGGGAGAGAAACTTATCCTAAGCACTCCTTATGAGTTGCTTGTGACA AAAAGTGAGGTCAGGGAAGGGGAGAGAAACTTGTCCTAAGCACTCCTTATGAGTTGCTTGTGACA T C KCNQ3 Ensembl:ENSG00000184156 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs563067190 Functional Loss SNV dbSNP153 33..33 33 - - - 16245 RMVar_ID_16245 Human_SNP_ID_382996656 A-to-I Human chr8 - 132295304 132295304 132295304 TTATCTCATTGTGGTTTGATTTGCATTTCTCTAATTATCAGTGATGTTGAGCATTTTTTCATGTT TTATCTCATTGTGGTTTGATTTGCATTTCTCTTATTATCAGTGATGTTGAGCATTTTTTCATGTT T A KCNQ3 Ensembl:ENSG00000184156 Protein coding intron GSE107867 ASD brains,frontal_cortex;ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs564794120 Functional Loss SNV dbSNP153 33..33 33 - - - 16246 RMVar_ID_16246 Human_SNP_ID_382996657 A-to-I Human chr8 - 132295304 132295304 132295304 TTATCTCATTGTGGTTTGATTTGCATTTCTCTAATTATCAGTGATGTTGAGCATTTTTTCATGTT TTATCTCATTGTGGTTTGATTTGCATTTCTCTGATTATCAGTGATGTTGAGCATTTTTTCATGTT T C KCNQ3 Ensembl:ENSG00000184156 Protein coding intron GSE107867 ASD brains,frontal_cortex;ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs564794120 Functional Loss SNV dbSNP153 33..33 33 - - - 16247 RMVar_ID_16247 Human_SNP_ID_383006813 A-to-I Human chr8 - 132337410 132337410 132337410 TATTGCAACCTCGACCTCCTTGGGCTCAAGCAATTCTCCTGCCTCAGCCCCCTGAGTAGCTGGCA TATTGCAACCTCGACCTCCTTGGGCTCAAGCAGTTCTCCTGCCTCAGCCCCCTGAGTAGCTGGCA T C KCNQ3 Ensembl:ENSG00000184156 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1198162067 Functional Loss SNV dbSNP153 33..33 33 - - - 16248 RMVar_ID_16248 Human_SNP_ID_383034509 A-to-I Human chr8 - 132452313 132452313 132452313 ATACTGCATGGCTCCACTTAAAAGAGGCACCTAGAGGAGTTTAATTCATAGAAATAGAGAGTGGG ATACTGCATGGCTCCACTTAAAAGAGGCACCTTGAGGAGTTTAATTCATAGAAATAGAGAGTGGG T A KCNQ3 Ensembl:ENSG00000184156 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1014568270 Functional Loss SNV dbSNP153 33..33 33 - - - 16249 RMVar_ID_16249 Human_SNP_ID_383034510 A-to-I Human chr8 - 132452313 132452313 132452313 ATACTGCATGGCTCCACTTAAAAGAGGCACCTAGAGGAGTTTAATTCATAGAAATAGAGAGTGGG ATACTGCATGGCTCCACTTAAAAGAGGCACCTGGAGGAGTTTAATTCATAGAAATAGAGAGTGGG T C KCNQ3 Ensembl:ENSG00000184156 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1014568270 Functional Loss SNV dbSNP153 33..33 33 - - - 16250 RMVar_ID_16250 Human_SNP_ID_383241498 A-to-I Human chr8 - 133279006 133279006 133279006 AAGCACCTATAACCCCAGCTACTTGGGGGCTGAGACAGGAGAATTGCTTGAACCTGGGAGGCAGA AAGCACCTATAACCCCAGCTACTTGGGGGCTGGGACAGGAGAATTGCTTGAACCTGGGAGGCAGA T C NDRG1 Ensembl:ENSG00000104419 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs3206045 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85942,RMVar_hsa_circ_254548,RMVar_hsa_circ_84661,RMVar_hsa_circ_108261,RMVar_hsa_circ_254553,RMVar_hsa_circ_254554,RMVar_hsa_circ_254555 16251 RMVar_ID_16251 Human_SNP_ID_383302373 A-to-I Human chr8 - 133519863 133519863 133519863 TCATTGCAGCTTCTGCCTCCCAGGTTCAAGCAATTCTTATGCCTCAGCCTCCCAAGTAGCTAGGA TCATTGCAGCTTCTGCCTCCCAGGTTCAAGCAGTTCTTATGCCTCAGCCTCCCAAGTAGCTAGGA T C ST3GAL1 Ensembl:ENSG00000008513 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs906238767 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94238,RMVar_hsa_circ_254566,RMVar_hsa_circ_48025 16252 RMVar_ID_16252 Human_SNP_ID_383640017 A-to-I Human chr8 - 134812730 134812730 134812730 ATAATACGATTGATTGACTGATTGATTGAGACAGAGTCTTGCTCTGTTGCCCAGGCTGGAGTACA ATAATACGATTGATTGACTGATTGATTGAGACGGAGTCTTGCTCTGTTGCCCAGGCTGGAGTACA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1196180419 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_254592,RMVar_hsa_circ_254593 16253 RMVar_ID_16253 Human_SNP_ID_341286330 A-to-I Human chr7 - 135430455 135430455 135430455 AATTTTTTGTCTTTGCAGAGACTGGGCTCGCTATGTTGCCCAGGTTGGTCTTGAACTACTGCCCT AATTTTTTGTCTTTGCAGAGACTGGGCTCGCTGTGTTGCCCAGGTTGGTCTTGAACTACTGCCCT T C CNOT4 Ensembl:ENSG00000080802 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs942019816 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1330453,Human_RBP_ID_16026262 RMVar_hsa_circ_74410,RMVar_hsa_circ_280888,RMVar_hsa_circ_299593,RMVar_hsa_circ_67531,RMVar_hsa_circ_365465 16254 RMVar_ID_16254 Human_SNP_ID_341289942 A-to-I Human chr7 - 135446006 135446006 135446006 GTGGTGGTGCACACCTGTGGTTCCAGCTACTCAGGTGGCTGAGGTGGGAGGATTTGCTTTATAAA GTGGTGGTGCACACCTGTGGTTCCAGCTACTCTGGTGGCTGAGGTGGGAGGATTTGCTTTATAAA T A CNOT4 Ensembl:ENSG00000080802 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985952040 Functional Loss SNV dbSNP153 33..33 33 - - - 16255 RMVar_ID_16255 Human_SNP_ID_341289943 A-to-I Human chr7 - 135446006 135446006 135446006 GTGGTGGTGCACACCTGTGGTTCCAGCTACTCAGGTGGCTGAGGTGGGAGGATTTGCTTTATAAA GTGGTGGTGCACACCTGTGGTTCCAGCTACTCGGGTGGCTGAGGTGGGAGGATTTGCTTTATAAA T C CNOT4 Ensembl:ENSG00000080802 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985952040 Functional Loss SNV dbSNP153 33..33 33 - - - 16256 RMVar_ID_16256 Human_SNP_ID_341295653 A-to-I Human chr7 - 135469920 135469920 135469920 CTACTCGGGAGGCTCAGGCAGGAGAATTGCTTAAACCTAGGAGGTGGAGGTTGCAATGGGCTGAG CTACTCGGGAGGCTCAGGCAGGAGAATTGCTTTAACCTAGGAGGTGGAGGTTGCAATGGGCTGAG T A CNOT4 Ensembl:ENSG00000080802 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1471536945 Functional Loss SNV dbSNP153 33..33 33 - - - 16257 RMVar_ID_16257 Human_SNP_ID_341298168 A-to-I Human chr7 - 135479650 135479650 135479650 CAAGCCATCCTCCTGCCTCCGCCTCCCAAAGCACTGGGATTACAGGTGTGAGCCACCTTGCCTGG CAAGCCATCCTCCTGCCTCCGCCTCCCAAAGCCCTGGGATTACAGGTGTGAGCCACCTTGCCTGG T G CNOT4 Ensembl:ENSG00000080802 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1463985389 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26075977 16258 RMVar_ID_16258 Human_SNP_ID_341302501 A-to-I Human chr7 - 135496883 135496883 135496883 AGGATCGCTTGAGCTTGATAGATCGAGGCTGCAGTGAGCTGTGATTGTGCCACTTCACTCCAGTC AGGATCGCTTGAGCTTGATAGATCGAGGCTGCCGTGAGCTGTGATTGTGCCACTTCACTCCAGTC T G CNOT4 Ensembl:ENSG00000080802 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893478530 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17577963,Human_RBP_ID_22483579 16259 RMVar_ID_16259 Human_SNP_ID_341302510 A-to-I Human chr7 - 135496922 135496922 135496922 CACTCATGTAGTCCCAGCTACTTGGGAGTTTAAGTGGGGAGGATCGCTTGAGCTTGATAGATCGA CACTCATGTAGTCCCAGCTACTTGGGAGTTTAGGTGGGGAGGATCGCTTGAGCTTGATAGATCGA T C CNOT4 Ensembl:ENSG00000080802 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1162083173 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17577963,Human_RBP_ID_22483579 16260 RMVar_ID_16260 Human_SNP_ID_341323744 A-to-I Human chr7 + 135580660 135580660 135580660 AAGTTTTTGTATTTTAGTAGAGACAGGGTTTCACCGGGTTGCCTAGGCTGGTCTCGAACTCCGGA AAGTTTTTGTATTTTAGTAGAGACAGGGTTTCGCCGGGTTGCCTAGGCTGGTCTCGAACTCCGGA A G NUP205 Ensembl:ENSG00000155561 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1434153752 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16028308,Human_RBP_ID_26076177 RMVar_hsa_circ_86746,RMVar_hsa_circ_47477,RMVar_hsa_circ_125111,RMVar_hsa_circ_248697,RMVar_hsa_circ_84915,RMVar_hsa_circ_91013,RMVar_hsa_circ_113024,RMVar_hsa_circ_17357,RMVar_hsa_circ_248700,RMVar_hsa_circ_111384,RMVar_hsa_circ_90453,RMVar_hsa_circ_83317,RMVar_hsa_circ_248709,RMVar_hsa_circ_128038,RMVar_hsa_circ_248702,RMVar_hsa_circ_248704,RMVar_hsa_circ_248705,RMVar_hsa_circ_248706,RMVar_hsa_circ_248703,RMVar_hsa_circ_308874,RMVar_hsa_circ_330511,RMVar_hsa_circ_248707,RMVar_hsa_circ_38445,RMVar_hsa_circ_300185,RMVar_hsa_circ_103578,RMVar_hsa_circ_122446,RMVar_hsa_circ_248708,RMVar_hsa_circ_275234,RMVar_hsa_circ_122445,RMVar_hsa_circ_94650,RMVar_hsa_circ_102235,RMVar_hsa_circ_92601,RMVar_hsa_circ_248712,RMVar_hsa_circ_248716,RMVar_hsa_circ_81993,RMVar_hsa_circ_86618,RMVar_hsa_circ_248718,RMVar_hsa_circ_248720,RMVar_hsa_circ_11655,RMVar_hsa_circ_248719,RMVar_hsa_circ_248717,RMVar_hsa_circ_248714,RMVar_hsa_circ_248715,RMVar_hsa_circ_248713,RMVar_hsa_circ_31081,RMVar_hsa_circ_126751,RMVar_hsa_circ_248711,RMVar_hsa_circ_265334,RMVar_hsa_circ_119584,RMVar_hsa_circ_248721,RMVar_hsa_circ_248722 16261 RMVar_ID_16261 Human_SNP_ID_341323754 A-to-I Human chr7 + 135580697 135580697 135580697 GTTGCCTAGGCTGGTCTCGAACTCCGGAGCTCAGGCAATCTGCCTGCCTTGGCCTCCCAAAGTGC GTTGCCTAGGCTGGTCTCGAACTCCGGAGCTCCGGCAATCTGCCTGCCTTGGCCTCCCAAAGTGC A C NUP205 Ensembl:ENSG00000155561 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1178385648 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86746,RMVar_hsa_circ_47477,RMVar_hsa_circ_125111,RMVar_hsa_circ_248697,RMVar_hsa_circ_84915,RMVar_hsa_circ_91013,RMVar_hsa_circ_113024,RMVar_hsa_circ_17357,RMVar_hsa_circ_248700,RMVar_hsa_circ_111384,RMVar_hsa_circ_90453,RMVar_hsa_circ_83317,RMVar_hsa_circ_248709,RMVar_hsa_circ_128038,RMVar_hsa_circ_248702,RMVar_hsa_circ_248704,RMVar_hsa_circ_248705,RMVar_hsa_circ_248706,RMVar_hsa_circ_248703,RMVar_hsa_circ_308874,RMVar_hsa_circ_330511,RMVar_hsa_circ_248707,RMVar_hsa_circ_38445,RMVar_hsa_circ_300185,RMVar_hsa_circ_103578,RMVar_hsa_circ_122446,RMVar_hsa_circ_248708,RMVar_hsa_circ_275234,RMVar_hsa_circ_122445,RMVar_hsa_circ_94650,RMVar_hsa_circ_102235,RMVar_hsa_circ_92601,RMVar_hsa_circ_248712,RMVar_hsa_circ_248716,RMVar_hsa_circ_81993,RMVar_hsa_circ_86618,RMVar_hsa_circ_248718,RMVar_hsa_circ_248720,RMVar_hsa_circ_11655,RMVar_hsa_circ_248719,RMVar_hsa_circ_248717,RMVar_hsa_circ_248714,RMVar_hsa_circ_248715,RMVar_hsa_circ_248713,RMVar_hsa_circ_31081,RMVar_hsa_circ_126751,RMVar_hsa_circ_248711,RMVar_hsa_circ_265334,RMVar_hsa_circ_119584,RMVar_hsa_circ_248721,RMVar_hsa_circ_248722 16262 RMVar_ID_16262 Human_SNP_ID_341323888 A-to-I Human chr7 + 135581286 135581286 135581286 AGGCATGAAGCCAGGTGCAGTGCCTCATGCCTATAATCCCAGCATTTTGGGAGGCCAAGGTGGGA AGGCATGAAGCCAGGTGCAGTGCCTCATGCCTGTAATCCCAGCATTTTGGGAGGCCAAGGTGGGA A G NUP205 Ensembl:ENSG00000155561 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1399975312 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86746,RMVar_hsa_circ_47477,RMVar_hsa_circ_125111,RMVar_hsa_circ_248697,RMVar_hsa_circ_84915,RMVar_hsa_circ_91013,RMVar_hsa_circ_113024,RMVar_hsa_circ_17357,RMVar_hsa_circ_248700,RMVar_hsa_circ_111384,RMVar_hsa_circ_90453,RMVar_hsa_circ_83317,RMVar_hsa_circ_248709,RMVar_hsa_circ_128038,RMVar_hsa_circ_248702,RMVar_hsa_circ_248704,RMVar_hsa_circ_248705,RMVar_hsa_circ_248706,RMVar_hsa_circ_248703,RMVar_hsa_circ_308874,RMVar_hsa_circ_330511,RMVar_hsa_circ_248707,RMVar_hsa_circ_38445,RMVar_hsa_circ_300185,RMVar_hsa_circ_103578,RMVar_hsa_circ_122446,RMVar_hsa_circ_248708,RMVar_hsa_circ_275234,RMVar_hsa_circ_122445,RMVar_hsa_circ_94650,RMVar_hsa_circ_102235,RMVar_hsa_circ_92601,RMVar_hsa_circ_248712,RMVar_hsa_circ_248716,RMVar_hsa_circ_81993,RMVar_hsa_circ_86618,RMVar_hsa_circ_248718,RMVar_hsa_circ_248720,RMVar_hsa_circ_11655,RMVar_hsa_circ_248719,RMVar_hsa_circ_248717,RMVar_hsa_circ_248714,RMVar_hsa_circ_248715,RMVar_hsa_circ_248713,RMVar_hsa_circ_31081,RMVar_hsa_circ_126751,RMVar_hsa_circ_248711,RMVar_hsa_circ_265334,RMVar_hsa_circ_119584,RMVar_hsa_circ_248721,RMVar_hsa_circ_248722 16263 RMVar_ID_16263 Human_SNP_ID_341324051 A-to-I Human chr7 + 135582014 135582014 135582014 TGGTCTTCAAGAAGTAATTTTTGGCTGGGCATAGTGGCTCATGCCTGTAATGTCAGTGCTTTGGG TGGTCTTCAAGAAGTAATTTTTGGCTGGGCATCGTGGCTCATGCCTGTAATGTCAGTGCTTTGGG A C NUP205 Ensembl:ENSG00000155561 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1489259556 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86746,RMVar_hsa_circ_47477,RMVar_hsa_circ_125111,RMVar_hsa_circ_248697,RMVar_hsa_circ_84915,RMVar_hsa_circ_91013,RMVar_hsa_circ_113024,RMVar_hsa_circ_17357,RMVar_hsa_circ_248700,RMVar_hsa_circ_111384,RMVar_hsa_circ_90453,RMVar_hsa_circ_83317,RMVar_hsa_circ_248709,RMVar_hsa_circ_128038,RMVar_hsa_circ_248702,RMVar_hsa_circ_248704,RMVar_hsa_circ_248705,RMVar_hsa_circ_248706,RMVar_hsa_circ_248703,RMVar_hsa_circ_308874,RMVar_hsa_circ_330511,RMVar_hsa_circ_248707,RMVar_hsa_circ_38445,RMVar_hsa_circ_300185,RMVar_hsa_circ_103578,RMVar_hsa_circ_122446,RMVar_hsa_circ_248708,RMVar_hsa_circ_275234,RMVar_hsa_circ_122445,RMVar_hsa_circ_94650,RMVar_hsa_circ_102235,RMVar_hsa_circ_92601,RMVar_hsa_circ_248712,RMVar_hsa_circ_248716,RMVar_hsa_circ_81993,RMVar_hsa_circ_86618,RMVar_hsa_circ_248718,RMVar_hsa_circ_248720,RMVar_hsa_circ_11655,RMVar_hsa_circ_248719,RMVar_hsa_circ_248717,RMVar_hsa_circ_248714,RMVar_hsa_circ_248715,RMVar_hsa_circ_248713,RMVar_hsa_circ_31081,RMVar_hsa_circ_126751,RMVar_hsa_circ_248711,RMVar_hsa_circ_265334,RMVar_hsa_circ_119584,RMVar_hsa_circ_248721,RMVar_hsa_circ_248722 16264 RMVar_ID_16264 Human_SNP_ID_341324052 A-to-I Human chr7 + 135582014 135582014 135582014 TGGTCTTCAAGAAGTAATTTTTGGCTGGGCATAGTGGCTCATGCCTGTAATGTCAGTGCTTTGGG TGGTCTTCAAGAAGTAATTTTTGGCTGGGCATGGTGGCTCATGCCTGTAATGTCAGTGCTTTGGG A G NUP205 Ensembl:ENSG00000155561 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1489259556 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86746,RMVar_hsa_circ_47477,RMVar_hsa_circ_125111,RMVar_hsa_circ_248697,RMVar_hsa_circ_84915,RMVar_hsa_circ_91013,RMVar_hsa_circ_113024,RMVar_hsa_circ_17357,RMVar_hsa_circ_248700,RMVar_hsa_circ_111384,RMVar_hsa_circ_90453,RMVar_hsa_circ_83317,RMVar_hsa_circ_248709,RMVar_hsa_circ_128038,RMVar_hsa_circ_248702,RMVar_hsa_circ_248704,RMVar_hsa_circ_248705,RMVar_hsa_circ_248706,RMVar_hsa_circ_248703,RMVar_hsa_circ_308874,RMVar_hsa_circ_330511,RMVar_hsa_circ_248707,RMVar_hsa_circ_38445,RMVar_hsa_circ_300185,RMVar_hsa_circ_103578,RMVar_hsa_circ_122446,RMVar_hsa_circ_248708,RMVar_hsa_circ_275234,RMVar_hsa_circ_122445,RMVar_hsa_circ_94650,RMVar_hsa_circ_102235,RMVar_hsa_circ_92601,RMVar_hsa_circ_248712,RMVar_hsa_circ_248716,RMVar_hsa_circ_81993,RMVar_hsa_circ_86618,RMVar_hsa_circ_248718,RMVar_hsa_circ_248720,RMVar_hsa_circ_11655,RMVar_hsa_circ_248719,RMVar_hsa_circ_248717,RMVar_hsa_circ_248714,RMVar_hsa_circ_248715,RMVar_hsa_circ_248713,RMVar_hsa_circ_31081,RMVar_hsa_circ_126751,RMVar_hsa_circ_248711,RMVar_hsa_circ_265334,RMVar_hsa_circ_119584,RMVar_hsa_circ_248721,RMVar_hsa_circ_248722 16265 RMVar_ID_16265 Human_SNP_ID_341324155 A-to-I Human chr7 + 135582510 135582510 135582510 GGTAGATAAGCACGTTTTTGTTTGTTTGAGATAGTGGCTTCCCTGTTGCCCAGGCTGGAGTGCAG GGTAGATAAGCACGTTTTTGTTTGTTTGAGATCGTGGCTTCCCTGTTGCCCAGGCTGGAGTGCAG A C NUP205 Ensembl:ENSG00000155561 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1484999041 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16028349 RMVar_hsa_circ_86746,RMVar_hsa_circ_47477,RMVar_hsa_circ_125111,RMVar_hsa_circ_248697,RMVar_hsa_circ_84915,RMVar_hsa_circ_91013,RMVar_hsa_circ_113024,RMVar_hsa_circ_17357,RMVar_hsa_circ_248700,RMVar_hsa_circ_111384,RMVar_hsa_circ_90453,RMVar_hsa_circ_83317,RMVar_hsa_circ_248709,RMVar_hsa_circ_128038,RMVar_hsa_circ_248702,RMVar_hsa_circ_248704,RMVar_hsa_circ_248705,RMVar_hsa_circ_248706,RMVar_hsa_circ_248703,RMVar_hsa_circ_308874,RMVar_hsa_circ_330511,RMVar_hsa_circ_248707,RMVar_hsa_circ_38445,RMVar_hsa_circ_300185,RMVar_hsa_circ_103578,RMVar_hsa_circ_122446,RMVar_hsa_circ_248708,RMVar_hsa_circ_275234,RMVar_hsa_circ_122445,RMVar_hsa_circ_94650,RMVar_hsa_circ_102235,RMVar_hsa_circ_92601,RMVar_hsa_circ_248712,RMVar_hsa_circ_248716,RMVar_hsa_circ_81993,RMVar_hsa_circ_86618,RMVar_hsa_circ_248718,RMVar_hsa_circ_248720,RMVar_hsa_circ_11655,RMVar_hsa_circ_248719,RMVar_hsa_circ_248717,RMVar_hsa_circ_248714,RMVar_hsa_circ_248715,RMVar_hsa_circ_248713,RMVar_hsa_circ_31081,RMVar_hsa_circ_126751,RMVar_hsa_circ_248711,RMVar_hsa_circ_265334,RMVar_hsa_circ_119584,RMVar_hsa_circ_248721,RMVar_hsa_circ_248722 16266 RMVar_ID_16266 Human_SNP_ID_341324191 A-to-I Human chr7 + 135582648 135582648 135582648 TGGGACCACAGCTAATTCTTTGATTTTTTTGTAGAGATGAGGTCTCACTATGTTGCCTAGGCTGG TGGGACCACAGCTAATTCTTTGATTTTTTTGTGGAGATGAGGTCTCACTATGTTGCCTAGGCTGG A G NUP205 Ensembl:ENSG00000155561 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1215160107 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17577965 RMVar_hsa_circ_86746,RMVar_hsa_circ_47477,RMVar_hsa_circ_125111,RMVar_hsa_circ_248697,RMVar_hsa_circ_84915,RMVar_hsa_circ_91013,RMVar_hsa_circ_113024,RMVar_hsa_circ_17357,RMVar_hsa_circ_248700,RMVar_hsa_circ_111384,RMVar_hsa_circ_90453,RMVar_hsa_circ_83317,RMVar_hsa_circ_248709,RMVar_hsa_circ_128038,RMVar_hsa_circ_248702,RMVar_hsa_circ_248704,RMVar_hsa_circ_248705,RMVar_hsa_circ_248706,RMVar_hsa_circ_248703,RMVar_hsa_circ_308874,RMVar_hsa_circ_330511,RMVar_hsa_circ_248707,RMVar_hsa_circ_38445,RMVar_hsa_circ_300185,RMVar_hsa_circ_103578,RMVar_hsa_circ_122446,RMVar_hsa_circ_248708,RMVar_hsa_circ_275234,RMVar_hsa_circ_122445,RMVar_hsa_circ_94650,RMVar_hsa_circ_102235,RMVar_hsa_circ_92601,RMVar_hsa_circ_248712,RMVar_hsa_circ_248716,RMVar_hsa_circ_81993,RMVar_hsa_circ_86618,RMVar_hsa_circ_248718,RMVar_hsa_circ_248720,RMVar_hsa_circ_11655,RMVar_hsa_circ_248719,RMVar_hsa_circ_248717,RMVar_hsa_circ_248714,RMVar_hsa_circ_248715,RMVar_hsa_circ_248713,RMVar_hsa_circ_31081,RMVar_hsa_circ_126751,RMVar_hsa_circ_248711,RMVar_hsa_circ_265334,RMVar_hsa_circ_119584,RMVar_hsa_circ_248721,RMVar_hsa_circ_248722 16267 RMVar_ID_16267 Human_SNP_ID_341324214 A-to-I Human chr7 + 135582734 135582734 135582734 CAATCCTCCTGTCTTGGCTAAGTGTTGGGATTACAGGCATGAGCCACCACACCTGGCTGATAATG CAATCCTCCTGTCTTGGCTAAGTGTTGGGATTTCAGGCATGAGCCACCACACCTGGCTGATAATG A T NUP205 Ensembl:ENSG00000155561 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1051610157 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17577966 RMVar_hsa_circ_86746,RMVar_hsa_circ_47477,RMVar_hsa_circ_125111,RMVar_hsa_circ_248697,RMVar_hsa_circ_84915,RMVar_hsa_circ_91013,RMVar_hsa_circ_113024,RMVar_hsa_circ_17357,RMVar_hsa_circ_248700,RMVar_hsa_circ_111384,RMVar_hsa_circ_90453,RMVar_hsa_circ_83317,RMVar_hsa_circ_248709,RMVar_hsa_circ_128038,RMVar_hsa_circ_248702,RMVar_hsa_circ_248704,RMVar_hsa_circ_248705,RMVar_hsa_circ_248706,RMVar_hsa_circ_248703,RMVar_hsa_circ_308874,RMVar_hsa_circ_330511,RMVar_hsa_circ_248707,RMVar_hsa_circ_38445,RMVar_hsa_circ_300185,RMVar_hsa_circ_103578,RMVar_hsa_circ_122446,RMVar_hsa_circ_248708,RMVar_hsa_circ_275234,RMVar_hsa_circ_122445,RMVar_hsa_circ_94650,RMVar_hsa_circ_102235,RMVar_hsa_circ_92601,RMVar_hsa_circ_248712,RMVar_hsa_circ_248716,RMVar_hsa_circ_81993,RMVar_hsa_circ_86618,RMVar_hsa_circ_248718,RMVar_hsa_circ_248720,RMVar_hsa_circ_11655,RMVar_hsa_circ_248719,RMVar_hsa_circ_248717,RMVar_hsa_circ_248714,RMVar_hsa_circ_248715,RMVar_hsa_circ_248713,RMVar_hsa_circ_31081,RMVar_hsa_circ_126751,RMVar_hsa_circ_248711,RMVar_hsa_circ_265334,RMVar_hsa_circ_119584,RMVar_hsa_circ_248721,RMVar_hsa_circ_248722 16268 RMVar_ID_16268 Human_SNP_ID_341325762 A-to-I Human chr7 + 135589125 135589125 135589125 CCCGGGGTTTGAGGTTACAGTGAGATGTGGTTACGCCACTGCACTCCAGCCTAGGCAACAGAGTG CCCGGGGTTTGAGGTTACAGTGAGATGTGGTTGCGCCACTGCACTCCAGCCTAGGCAACAGAGTG A G NUP205 Ensembl:ENSG00000155561 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs71539417 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15058,RMVar_hsa_circ_86746,RMVar_hsa_circ_125111,RMVar_hsa_circ_248697,RMVar_hsa_circ_84915,RMVar_hsa_circ_91013,RMVar_hsa_circ_113024,RMVar_hsa_circ_17357,RMVar_hsa_circ_248700,RMVar_hsa_circ_111384,RMVar_hsa_circ_90453,RMVar_hsa_circ_83317,RMVar_hsa_circ_128038,RMVar_hsa_circ_248702,RMVar_hsa_circ_248704,RMVar_hsa_circ_248705,RMVar_hsa_circ_248706,RMVar_hsa_circ_248703,RMVar_hsa_circ_330511,RMVar_hsa_circ_248707,RMVar_hsa_circ_38445,RMVar_hsa_circ_103578,RMVar_hsa_circ_122446,RMVar_hsa_circ_248708,RMVar_hsa_circ_275234,RMVar_hsa_circ_122445,RMVar_hsa_circ_94650,RMVar_hsa_circ_102235,RMVar_hsa_circ_92601,RMVar_hsa_circ_248712,RMVar_hsa_circ_248716,RMVar_hsa_circ_81993,RMVar_hsa_circ_86618,RMVar_hsa_circ_248718,RMVar_hsa_circ_248720,RMVar_hsa_circ_11655,RMVar_hsa_circ_248719,RMVar_hsa_circ_248717,RMVar_hsa_circ_248714,RMVar_hsa_circ_248715,RMVar_hsa_circ_248713,RMVar_hsa_circ_31081,RMVar_hsa_circ_248711,RMVar_hsa_circ_265334,RMVar_hsa_circ_119584,RMVar_hsa_circ_66700,RMVar_hsa_circ_248721,RMVar_hsa_circ_325187,RMVar_hsa_circ_351214,RMVar_hsa_circ_271377,RMVar_hsa_circ_299148,RMVar_hsa_circ_95158,RMVar_hsa_circ_42060,RMVar_hsa_circ_42779,RMVar_hsa_circ_34859,RMVar_hsa_circ_57289,RMVar_hsa_circ_248724,RMVar_hsa_circ_248726,RMVar_hsa_circ_248727,RMVar_hsa_circ_248725,RMVar_hsa_circ_347336,RMVar_hsa_circ_315839,RMVar_hsa_circ_48300,RMVar_hsa_circ_248728 16269 RMVar_ID_16269 Human_SNP_ID_341325849 A-to-I Human chr7 + 135589430 135589430 135589430 CCTGTCTCAGCCTCCCGAATAACTGGGGTTATAGACATGCGCCACCACGCCAGGCTAATTTTGTA CCTGTCTCAGCCTCCCGAATAACTGGGGTTATGGACATGCGCCACCACGCCAGGCTAATTTTGTA A G NUP205 Ensembl:ENSG00000155561 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444364904 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15058,RMVar_hsa_circ_86746,RMVar_hsa_circ_125111,RMVar_hsa_circ_248697,RMVar_hsa_circ_84915,RMVar_hsa_circ_91013,RMVar_hsa_circ_113024,RMVar_hsa_circ_17357,RMVar_hsa_circ_248700,RMVar_hsa_circ_111384,RMVar_hsa_circ_90453,RMVar_hsa_circ_83317,RMVar_hsa_circ_128038,RMVar_hsa_circ_248702,RMVar_hsa_circ_248704,RMVar_hsa_circ_248705,RMVar_hsa_circ_248706,RMVar_hsa_circ_248703,RMVar_hsa_circ_330511,RMVar_hsa_circ_248707,RMVar_hsa_circ_38445,RMVar_hsa_circ_103578,RMVar_hsa_circ_122446,RMVar_hsa_circ_248708,RMVar_hsa_circ_275234,RMVar_hsa_circ_122445,RMVar_hsa_circ_94650,RMVar_hsa_circ_102235,RMVar_hsa_circ_92601,RMVar_hsa_circ_248712,RMVar_hsa_circ_248716,RMVar_hsa_circ_81993,RMVar_hsa_circ_86618,RMVar_hsa_circ_248718,RMVar_hsa_circ_248720,RMVar_hsa_circ_11655,RMVar_hsa_circ_248719,RMVar_hsa_circ_248717,RMVar_hsa_circ_248714,RMVar_hsa_circ_248715,RMVar_hsa_circ_248713,RMVar_hsa_circ_31081,RMVar_hsa_circ_248711,RMVar_hsa_circ_265334,RMVar_hsa_circ_119584,RMVar_hsa_circ_66700,RMVar_hsa_circ_248721,RMVar_hsa_circ_325187,RMVar_hsa_circ_351214,RMVar_hsa_circ_271377,RMVar_hsa_circ_299148,RMVar_hsa_circ_95158,RMVar_hsa_circ_42060,RMVar_hsa_circ_42779,RMVar_hsa_circ_34859,RMVar_hsa_circ_57289,RMVar_hsa_circ_248724,RMVar_hsa_circ_248726,RMVar_hsa_circ_248727,RMVar_hsa_circ_248725,RMVar_hsa_circ_347336,RMVar_hsa_circ_315839,RMVar_hsa_circ_48300,RMVar_hsa_circ_248728 16270 RMVar_ID_16270 Human_SNP_ID_341325934 A-to-I Human chr7 + 135589810 135589810 135589810 TAAAAATTAGCCAGACATGGTGGTGCGTACCTATGGCCCCATTTGCACGGGAGGCTGAGGTGGGA TAAAAATTAGCCAGACATGGTGGTGCGTACCTGTGGCCCCATTTGCACGGGAGGCTGAGGTGGGA A G NUP205 Ensembl:ENSG00000155561 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1180957817 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15058,RMVar_hsa_circ_86746,RMVar_hsa_circ_125111,RMVar_hsa_circ_248697,RMVar_hsa_circ_84915,RMVar_hsa_circ_91013,RMVar_hsa_circ_113024,RMVar_hsa_circ_17357,RMVar_hsa_circ_248700,RMVar_hsa_circ_111384,RMVar_hsa_circ_90453,RMVar_hsa_circ_83317,RMVar_hsa_circ_128038,RMVar_hsa_circ_248702,RMVar_hsa_circ_248704,RMVar_hsa_circ_248705,RMVar_hsa_circ_248706,RMVar_hsa_circ_248703,RMVar_hsa_circ_330511,RMVar_hsa_circ_248707,RMVar_hsa_circ_38445,RMVar_hsa_circ_103578,RMVar_hsa_circ_122446,RMVar_hsa_circ_248708,RMVar_hsa_circ_275234,RMVar_hsa_circ_122445,RMVar_hsa_circ_94650,RMVar_hsa_circ_102235,RMVar_hsa_circ_92601,RMVar_hsa_circ_248712,RMVar_hsa_circ_248716,RMVar_hsa_circ_81993,RMVar_hsa_circ_86618,RMVar_hsa_circ_248718,RMVar_hsa_circ_248720,RMVar_hsa_circ_11655,RMVar_hsa_circ_248719,RMVar_hsa_circ_248717,RMVar_hsa_circ_248714,RMVar_hsa_circ_248715,RMVar_hsa_circ_248713,RMVar_hsa_circ_31081,RMVar_hsa_circ_248711,RMVar_hsa_circ_265334,RMVar_hsa_circ_119584,RMVar_hsa_circ_66700,RMVar_hsa_circ_248721,RMVar_hsa_circ_325187,RMVar_hsa_circ_351214,RMVar_hsa_circ_271377,RMVar_hsa_circ_299148,RMVar_hsa_circ_95158,RMVar_hsa_circ_42060,RMVar_hsa_circ_42779,RMVar_hsa_circ_34859,RMVar_hsa_circ_57289,RMVar_hsa_circ_248724,RMVar_hsa_circ_248726,RMVar_hsa_circ_248727,RMVar_hsa_circ_248725,RMVar_hsa_circ_347336,RMVar_hsa_circ_315839,RMVar_hsa_circ_48300,RMVar_hsa_circ_248728 16271 RMVar_ID_16271 Human_SNP_ID_341327272 A-to-I Human chr7 + 135595238 135595238 135595238 CAAGTTTGCACTGATTTTTGTTTTTTTTTTTTAAGATAGGGTCTCGCTGTGTTGGCAAGGATGGA CAAGTTTGCACTGATTTTTGTTTTTTTTTTTTTAGATAGGGTCTCGCTGTGTTGGCAAGGATGGA A T NUP205 Ensembl:ENSG00000155561 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1255775270 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7701307,Human_RBP_ID_16028598 RMVar_hsa_circ_15058,RMVar_hsa_circ_86746,RMVar_hsa_circ_84915,RMVar_hsa_circ_113024,RMVar_hsa_circ_248700,RMVar_hsa_circ_111384,RMVar_hsa_circ_90453,RMVar_hsa_circ_83317,RMVar_hsa_circ_248704,RMVar_hsa_circ_248705,RMVar_hsa_circ_248706,RMVar_hsa_circ_248703,RMVar_hsa_circ_103578,RMVar_hsa_circ_122446,RMVar_hsa_circ_122445,RMVar_hsa_circ_94650,RMVar_hsa_circ_102235,RMVar_hsa_circ_92601,RMVar_hsa_circ_248712,RMVar_hsa_circ_248716,RMVar_hsa_circ_81993,RMVar_hsa_circ_86618,RMVar_hsa_circ_248718,RMVar_hsa_circ_248720,RMVar_hsa_circ_11655,RMVar_hsa_circ_248719,RMVar_hsa_circ_248717,RMVar_hsa_circ_248714,RMVar_hsa_circ_248715,RMVar_hsa_circ_248713,RMVar_hsa_circ_31081,RMVar_hsa_circ_119584,RMVar_hsa_circ_66700,RMVar_hsa_circ_248721,RMVar_hsa_circ_325187,RMVar_hsa_circ_351214,RMVar_hsa_circ_299148,RMVar_hsa_circ_95158,RMVar_hsa_circ_42779,RMVar_hsa_circ_34859,RMVar_hsa_circ_27495,RMVar_hsa_circ_248726,RMVar_hsa_circ_248727,RMVar_hsa_circ_248725,RMVar_hsa_circ_48300,RMVar_hsa_circ_248730,RMVar_hsa_circ_112458,RMVar_hsa_circ_269435,RMVar_hsa_circ_104561,RMVar_hsa_circ_248732 16272 RMVar_ID_16272 Human_SNP_ID_341327500 A-to-I Human chr7 + 135596199 135596199 135596199 CAGGTGATCCGCCTGCCTTGGCCTCCCAAAGTACTGGGATTACAGGCGTGAGCCACCACGCCCAG CAGGTGATCCGCCTGCCTTGGCCTCCCAAAGTCCTGGGATTACAGGCGTGAGCCACCACGCCCAG A C NUP205 Ensembl:ENSG00000155561 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1465253163 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15058,RMVar_hsa_circ_86746,RMVar_hsa_circ_84915,RMVar_hsa_circ_113024,RMVar_hsa_circ_248700,RMVar_hsa_circ_111384,RMVar_hsa_circ_90453,RMVar_hsa_circ_83317,RMVar_hsa_circ_248704,RMVar_hsa_circ_248705,RMVar_hsa_circ_248706,RMVar_hsa_circ_248703,RMVar_hsa_circ_103578,RMVar_hsa_circ_122446,RMVar_hsa_circ_122445,RMVar_hsa_circ_94650,RMVar_hsa_circ_102235,RMVar_hsa_circ_92601,RMVar_hsa_circ_248712,RMVar_hsa_circ_248716,RMVar_hsa_circ_81993,RMVar_hsa_circ_86618,RMVar_hsa_circ_248718,RMVar_hsa_circ_248720,RMVar_hsa_circ_11655,RMVar_hsa_circ_248719,RMVar_hsa_circ_248717,RMVar_hsa_circ_248714,RMVar_hsa_circ_248715,RMVar_hsa_circ_248713,RMVar_hsa_circ_31081,RMVar_hsa_circ_119584,RMVar_hsa_circ_66700,RMVar_hsa_circ_248721,RMVar_hsa_circ_325187,RMVar_hsa_circ_351214,RMVar_hsa_circ_299148,RMVar_hsa_circ_95158,RMVar_hsa_circ_42779,RMVar_hsa_circ_34859,RMVar_hsa_circ_27495,RMVar_hsa_circ_248726,RMVar_hsa_circ_248727,RMVar_hsa_circ_248725,RMVar_hsa_circ_48300,RMVar_hsa_circ_248730,RMVar_hsa_circ_112458,RMVar_hsa_circ_269435,RMVar_hsa_circ_104561,RMVar_hsa_circ_248732 16273 RMVar_ID_16273 Human_SNP_ID_341330605 A-to-I Human chr7 + 135608898 135608897 135608898 TAAGGTGAGCAGATCACCTGAGGTTAGGAGTTAGAGACCAGCCTGGCCAACATGGTGGAACCCCA TAAGGTGAGCAGATCACCTGAGGTTAGGAGTT_GAGACCAGCCTGGCCAACATGGTGGAACCCCA TA T NUP205 Ensembl:ENSG00000155561 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs879075749 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_15058,RMVar_hsa_circ_86746,RMVar_hsa_circ_84915,RMVar_hsa_circ_248700,RMVar_hsa_circ_111384,RMVar_hsa_circ_90453,RMVar_hsa_circ_83317,RMVar_hsa_circ_248704,RMVar_hsa_circ_248705,RMVar_hsa_circ_248706,RMVar_hsa_circ_103578,RMVar_hsa_circ_122446,RMVar_hsa_circ_102235,RMVar_hsa_circ_92601,RMVar_hsa_circ_248716,RMVar_hsa_circ_81993,RMVar_hsa_circ_86618,RMVar_hsa_circ_248718,RMVar_hsa_circ_248720,RMVar_hsa_circ_248719,RMVar_hsa_circ_248717,RMVar_hsa_circ_248714,RMVar_hsa_circ_248715,RMVar_hsa_circ_119584,RMVar_hsa_circ_66700,RMVar_hsa_circ_248721,RMVar_hsa_circ_351214,RMVar_hsa_circ_299148,RMVar_hsa_circ_95158,RMVar_hsa_circ_42779,RMVar_hsa_circ_34859,RMVar_hsa_circ_1470,RMVar_hsa_circ_248726,RMVar_hsa_circ_248727,RMVar_hsa_circ_248730,RMVar_hsa_circ_112458,RMVar_hsa_circ_269435,RMVar_hsa_circ_104561,RMVar_hsa_circ_23088,RMVar_hsa_circ_248733,RMVar_hsa_circ_86607,RMVar_hsa_circ_122892,RMVar_hsa_circ_248732,RMVar_hsa_circ_248734,RMVar_hsa_circ_73284,RMVar_hsa_circ_314157,RMVar_hsa_circ_107186,RMVar_hsa_circ_17793,RMVar_hsa_circ_12513,RMVar_hsa_circ_248735,RMVar_hsa_circ_51525,RMVar_hsa_circ_117240,RMVar_hsa_circ_48446,RMVar_hsa_circ_248739,RMVar_hsa_circ_71264,RMVar_hsa_circ_30475,RMVar_hsa_circ_67000,RMVar_hsa_circ_11615,RMVar_hsa_circ_111579,RMVar_hsa_circ_339118,RMVar_hsa_circ_16173,RMVar_hsa_circ_248742,RMVar_hsa_circ_338789,RMVar_hsa_circ_362478,RMVar_hsa_circ_331638,RMVar_hsa_circ_89539,RMVar_hsa_circ_248744,RMVar_hsa_circ_248745 16274 RMVar_ID_16274 Human_SNP_ID_341330616 A-to-I Human chr7 + 135608930 135608930 135608930 AGAGACCAGCCTGGCCAACATGGTGGAACCCCATCTCTACTAAAAATACAAAAAAAATTAGCTGG AGAGACCAGCCTGGCCAACATGGTGGAACCCCGTCTCTACTAAAAATACAAAAAAAATTAGCTGG A G NUP205 Ensembl:ENSG00000155561 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs955727378 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15058,RMVar_hsa_circ_86746,RMVar_hsa_circ_84915,RMVar_hsa_circ_248700,RMVar_hsa_circ_111384,RMVar_hsa_circ_90453,RMVar_hsa_circ_83317,RMVar_hsa_circ_248704,RMVar_hsa_circ_248705,RMVar_hsa_circ_248706,RMVar_hsa_circ_103578,RMVar_hsa_circ_122446,RMVar_hsa_circ_102235,RMVar_hsa_circ_92601,RMVar_hsa_circ_248716,RMVar_hsa_circ_81993,RMVar_hsa_circ_86618,RMVar_hsa_circ_248718,RMVar_hsa_circ_248720,RMVar_hsa_circ_248719,RMVar_hsa_circ_248717,RMVar_hsa_circ_248714,RMVar_hsa_circ_248715,RMVar_hsa_circ_119584,RMVar_hsa_circ_66700,RMVar_hsa_circ_248721,RMVar_hsa_circ_351214,RMVar_hsa_circ_299148,RMVar_hsa_circ_95158,RMVar_hsa_circ_42779,RMVar_hsa_circ_34859,RMVar_hsa_circ_1470,RMVar_hsa_circ_248726,RMVar_hsa_circ_248727,RMVar_hsa_circ_248730,RMVar_hsa_circ_112458,RMVar_hsa_circ_269435,RMVar_hsa_circ_104561,RMVar_hsa_circ_23088,RMVar_hsa_circ_248733,RMVar_hsa_circ_86607,RMVar_hsa_circ_122892,RMVar_hsa_circ_248732,RMVar_hsa_circ_248734,RMVar_hsa_circ_73284,RMVar_hsa_circ_314157,RMVar_hsa_circ_107186,RMVar_hsa_circ_17793,RMVar_hsa_circ_12513,RMVar_hsa_circ_248735,RMVar_hsa_circ_51525,RMVar_hsa_circ_117240,RMVar_hsa_circ_48446,RMVar_hsa_circ_248739,RMVar_hsa_circ_71264,RMVar_hsa_circ_30475,RMVar_hsa_circ_67000,RMVar_hsa_circ_11615,RMVar_hsa_circ_111579,RMVar_hsa_circ_339118,RMVar_hsa_circ_16173,RMVar_hsa_circ_248742,RMVar_hsa_circ_338789,RMVar_hsa_circ_362478,RMVar_hsa_circ_331638,RMVar_hsa_circ_89539,RMVar_hsa_circ_248744,RMVar_hsa_circ_248745 16275 RMVar_ID_16275 Human_SNP_ID_341331424 A-to-I Human chr7 + 135612005 135612005 135612005 AGCCGGGTATGGTGGTGGGCACCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCGGGAGAATGGCA AGCCGGGTATGGTGGTGGGCACCTGTAGTCCCGGCTACTCAGGAGGCTGAGGCGGGAGAATGGCA A G NUP205 Ensembl:ENSG00000155561 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs142392801 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_1142,GWAS_ID_1143,GWAS_ID_1144,GWAS_ID_1145,GWAS_ID_1146,GWAS_ID_1147,GWAS_ID_1148,GWAS_ID_1149,GWAS_ID_1150,GWAS_ID_1151,GWAS_ID_1152 RMVar_hsa_circ_15058,RMVar_hsa_circ_86746,RMVar_hsa_circ_84915,RMVar_hsa_circ_248700,RMVar_hsa_circ_111384,RMVar_hsa_circ_90453,RMVar_hsa_circ_83317,RMVar_hsa_circ_248704,RMVar_hsa_circ_248705,RMVar_hsa_circ_248706,RMVar_hsa_circ_103578,RMVar_hsa_circ_122446,RMVar_hsa_circ_102235,RMVar_hsa_circ_92601,RMVar_hsa_circ_248716,RMVar_hsa_circ_81993,RMVar_hsa_circ_86618,RMVar_hsa_circ_248718,RMVar_hsa_circ_248720,RMVar_hsa_circ_248719,RMVar_hsa_circ_248717,RMVar_hsa_circ_248714,RMVar_hsa_circ_248715,RMVar_hsa_circ_119584,RMVar_hsa_circ_66700,RMVar_hsa_circ_248721,RMVar_hsa_circ_351214,RMVar_hsa_circ_299148,RMVar_hsa_circ_95158,RMVar_hsa_circ_42779,RMVar_hsa_circ_34859,RMVar_hsa_circ_1470,RMVar_hsa_circ_248726,RMVar_hsa_circ_248727,RMVar_hsa_circ_248730,RMVar_hsa_circ_112458,RMVar_hsa_circ_269435,RMVar_hsa_circ_104561,RMVar_hsa_circ_23088,RMVar_hsa_circ_248733,RMVar_hsa_circ_86607,RMVar_hsa_circ_122892,RMVar_hsa_circ_248732,RMVar_hsa_circ_248734,RMVar_hsa_circ_73284,RMVar_hsa_circ_314157,RMVar_hsa_circ_107186,RMVar_hsa_circ_17793,RMVar_hsa_circ_12513,RMVar_hsa_circ_248735,RMVar_hsa_circ_51525,RMVar_hsa_circ_117240,RMVar_hsa_circ_48446,RMVar_hsa_circ_248739,RMVar_hsa_circ_71264,RMVar_hsa_circ_30475,RMVar_hsa_circ_67000,RMVar_hsa_circ_11615,RMVar_hsa_circ_111579,RMVar_hsa_circ_339118,RMVar_hsa_circ_16173,RMVar_hsa_circ_248742,RMVar_hsa_circ_338789,RMVar_hsa_circ_362478,RMVar_hsa_circ_331638,RMVar_hsa_circ_89539,RMVar_hsa_circ_248744,RMVar_hsa_circ_248745 16276 RMVar_ID_16276 Human_SNP_ID_341331859 A-to-I Human chr7 + 135613711 135613711 135613711 GGCACACGCTACCATGCCTGGCTAATTTTTGTATTTTTATAGAGACAGAGTTTCACCATGTTGAG GGCACACGCTACCATGCCTGGCTAATTTTTGTGTTTTTATAGAGACAGAGTTTCACCATGTTGAG A G NUP205 Ensembl:ENSG00000155561 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1159167924 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16029298 Human_Splice_Rec_926441 RMVar_hsa_circ_15058,RMVar_hsa_circ_86746,RMVar_hsa_circ_84915,RMVar_hsa_circ_248700,RMVar_hsa_circ_111384,RMVar_hsa_circ_90453,RMVar_hsa_circ_83317,RMVar_hsa_circ_248704,RMVar_hsa_circ_248705,RMVar_hsa_circ_248706,RMVar_hsa_circ_103578,RMVar_hsa_circ_122446,RMVar_hsa_circ_102235,RMVar_hsa_circ_92601,RMVar_hsa_circ_248716,RMVar_hsa_circ_81993,RMVar_hsa_circ_86618,RMVar_hsa_circ_248718,RMVar_hsa_circ_248720,RMVar_hsa_circ_248719,RMVar_hsa_circ_248717,RMVar_hsa_circ_248714,RMVar_hsa_circ_248715,RMVar_hsa_circ_119584,RMVar_hsa_circ_66700,RMVar_hsa_circ_248721,RMVar_hsa_circ_351214,RMVar_hsa_circ_299148,RMVar_hsa_circ_95158,RMVar_hsa_circ_42779,RMVar_hsa_circ_34859,RMVar_hsa_circ_1470,RMVar_hsa_circ_248726,RMVar_hsa_circ_248727,RMVar_hsa_circ_248730,RMVar_hsa_circ_112458,RMVar_hsa_circ_269435,RMVar_hsa_circ_104561,RMVar_hsa_circ_23088,RMVar_hsa_circ_248733,RMVar_hsa_circ_86607,RMVar_hsa_circ_122892,RMVar_hsa_circ_248732,RMVar_hsa_circ_248734,RMVar_hsa_circ_73284,RMVar_hsa_circ_314157,RMVar_hsa_circ_107186,RMVar_hsa_circ_17793,RMVar_hsa_circ_12513,RMVar_hsa_circ_248735,RMVar_hsa_circ_51525,RMVar_hsa_circ_117240,RMVar_hsa_circ_48446,RMVar_hsa_circ_248739,RMVar_hsa_circ_71264,RMVar_hsa_circ_30475,RMVar_hsa_circ_67000,RMVar_hsa_circ_11615,RMVar_hsa_circ_111579,RMVar_hsa_circ_339118,RMVar_hsa_circ_16173,RMVar_hsa_circ_248742,RMVar_hsa_circ_338789,RMVar_hsa_circ_362478,RMVar_hsa_circ_331638,RMVar_hsa_circ_89539,RMVar_hsa_circ_248744,RMVar_hsa_circ_248745 16277 RMVar_ID_16277 Human_SNP_ID_341331861 A-to-I Human chr7 + 135613719 135613719 135613719 CTACCATGCCTGGCTAATTTTTGTATTTTTATAGAGACAGAGTTTCACCATGTTGAGCAGACTGG CTACCATGCCTGGCTAATTTTTGTATTTTTATGGAGACAGAGTTTCACCATGTTGAGCAGACTGG A G NUP205 Ensembl:ENSG00000155561 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs865848489 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16029298 Human_Splice_Rec_926441 RMVar_hsa_circ_15058,RMVar_hsa_circ_86746,RMVar_hsa_circ_84915,RMVar_hsa_circ_248700,RMVar_hsa_circ_111384,RMVar_hsa_circ_90453,RMVar_hsa_circ_83317,RMVar_hsa_circ_248704,RMVar_hsa_circ_248705,RMVar_hsa_circ_248706,RMVar_hsa_circ_103578,RMVar_hsa_circ_122446,RMVar_hsa_circ_102235,RMVar_hsa_circ_92601,RMVar_hsa_circ_248716,RMVar_hsa_circ_81993,RMVar_hsa_circ_86618,RMVar_hsa_circ_248718,RMVar_hsa_circ_248720,RMVar_hsa_circ_248719,RMVar_hsa_circ_248717,RMVar_hsa_circ_248714,RMVar_hsa_circ_248715,RMVar_hsa_circ_119584,RMVar_hsa_circ_66700,RMVar_hsa_circ_248721,RMVar_hsa_circ_351214,RMVar_hsa_circ_299148,RMVar_hsa_circ_95158,RMVar_hsa_circ_42779,RMVar_hsa_circ_34859,RMVar_hsa_circ_1470,RMVar_hsa_circ_248726,RMVar_hsa_circ_248727,RMVar_hsa_circ_248730,RMVar_hsa_circ_112458,RMVar_hsa_circ_269435,RMVar_hsa_circ_104561,RMVar_hsa_circ_23088,RMVar_hsa_circ_248733,RMVar_hsa_circ_86607,RMVar_hsa_circ_122892,RMVar_hsa_circ_248732,RMVar_hsa_circ_248734,RMVar_hsa_circ_73284,RMVar_hsa_circ_314157,RMVar_hsa_circ_107186,RMVar_hsa_circ_17793,RMVar_hsa_circ_12513,RMVar_hsa_circ_248735,RMVar_hsa_circ_51525,RMVar_hsa_circ_117240,RMVar_hsa_circ_48446,RMVar_hsa_circ_248739,RMVar_hsa_circ_71264,RMVar_hsa_circ_30475,RMVar_hsa_circ_67000,RMVar_hsa_circ_11615,RMVar_hsa_circ_111579,RMVar_hsa_circ_339118,RMVar_hsa_circ_16173,RMVar_hsa_circ_248742,RMVar_hsa_circ_338789,RMVar_hsa_circ_362478,RMVar_hsa_circ_331638,RMVar_hsa_circ_89539,RMVar_hsa_circ_248744,RMVar_hsa_circ_248745 16278 RMVar_ID_16278 Human_SNP_ID_341331865 A-to-I Human chr7 + 135613736 135613736 135613736 TTTTTGTATTTTTATAGAGACAGAGTTTCACCATGTTGAGCAGACTGGTCTCAAACTCCTGACCT TTTTTGTATTTTTATAGAGACAGAGTTTCACCGTGTTGAGCAGACTGGTCTCAAACTCCTGACCT A G NUP205 Ensembl:ENSG00000155561 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1209088460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16029299 Human_Splice_Rec_926440,Human_Splice_Rec_926441 RMVar_hsa_circ_15058,RMVar_hsa_circ_86746,RMVar_hsa_circ_84915,RMVar_hsa_circ_248700,RMVar_hsa_circ_111384,RMVar_hsa_circ_90453,RMVar_hsa_circ_83317,RMVar_hsa_circ_248704,RMVar_hsa_circ_248705,RMVar_hsa_circ_248706,RMVar_hsa_circ_103578,RMVar_hsa_circ_122446,RMVar_hsa_circ_102235,RMVar_hsa_circ_92601,RMVar_hsa_circ_248716,RMVar_hsa_circ_81993,RMVar_hsa_circ_86618,RMVar_hsa_circ_248718,RMVar_hsa_circ_248720,RMVar_hsa_circ_248719,RMVar_hsa_circ_248717,RMVar_hsa_circ_248714,RMVar_hsa_circ_248715,RMVar_hsa_circ_119584,RMVar_hsa_circ_66700,RMVar_hsa_circ_248721,RMVar_hsa_circ_351214,RMVar_hsa_circ_299148,RMVar_hsa_circ_95158,RMVar_hsa_circ_42779,RMVar_hsa_circ_34859,RMVar_hsa_circ_1470,RMVar_hsa_circ_248726,RMVar_hsa_circ_248727,RMVar_hsa_circ_248730,RMVar_hsa_circ_112458,RMVar_hsa_circ_269435,RMVar_hsa_circ_104561,RMVar_hsa_circ_23088,RMVar_hsa_circ_248733,RMVar_hsa_circ_86607,RMVar_hsa_circ_122892,RMVar_hsa_circ_248732,RMVar_hsa_circ_248734,RMVar_hsa_circ_73284,RMVar_hsa_circ_314157,RMVar_hsa_circ_107186,RMVar_hsa_circ_17793,RMVar_hsa_circ_12513,RMVar_hsa_circ_248735,RMVar_hsa_circ_51525,RMVar_hsa_circ_117240,RMVar_hsa_circ_48446,RMVar_hsa_circ_248739,RMVar_hsa_circ_71264,RMVar_hsa_circ_30475,RMVar_hsa_circ_67000,RMVar_hsa_circ_11615,RMVar_hsa_circ_111579,RMVar_hsa_circ_339118,RMVar_hsa_circ_16173,RMVar_hsa_circ_248742,RMVar_hsa_circ_338789,RMVar_hsa_circ_362478,RMVar_hsa_circ_331638,RMVar_hsa_circ_89539,RMVar_hsa_circ_248744,RMVar_hsa_circ_248745 16279 RMVar_ID_16279 Human_SNP_ID_341339879 A-to-I Human chr7 + 135646487 135646487 135646487 AGGCTGAGGTGGGAGAATCACCTGAGCCTGGGAGACTGAGGCTGCAGTGAGCTGTGATTGCACCA AGGCTGAGGTGGGAGAATCACCTGAGCCTGGGGGACTGAGGCTGCAGTGAGCTGTGATTGCACCA A G NUP205 Ensembl:ENSG00000155561 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs987639506 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111384,RMVar_hsa_circ_248706 16280 RMVar_ID_16280 Human_SNP_ID_341348023 A-to-I Human chr7 + 135680334 135680334 135680334 CACCACCACGCCCGGCTAATTTTTGTATTTTTAGTAGAGTCGGGGTTTCACTCTACTAAAACCCT CACCACCACGCCCGGCTAATTTTTGTATTTTTGGTAGAGTCGGGGTTTCACTCTACTAAAACCCT A G STMP1 Ensembl:ENSG00000243317 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1040713070 Functional Loss SNV dbSNP153 33..33 33 - - - 16281 RMVar_ID_16281 Human_SNP_ID_341349621 A-to-I Human chr7 + 135686475 135686475 135686475 ACAGCTCACTGCAGTCTCAACCTCCTGGGTTCAAGCAATCCTCCCACCTCAGCCTTCCAAGTAGC ACAGCTCACTGCAGTCTCAACCTCCTGGGTTCGAGCAATCCTCCCACCTCAGCCTTCCAAGTAGC A G STMP1 Ensembl:ENSG00000243317 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs574266558 Functional Loss SNV dbSNP153 33..33 33 - - - 16282 RMVar_ID_16282 Human_SNP_ID_341884955 A-to-I Human chr7 - 137888081 137888081 137888081 ATGATGACTCACACCTGTATTCCCTCCCAGCTACTCAGGAGGCTGAGGCAGGAGGATTGCTCGAG ATGATGACTCACACCTGTATTCCCTCCCAGCTGCTCAGGAGGCTGAGGCAGGAGGATTGCTCGAG T C CREB3L2 Ensembl:ENSG00000182158 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1305579195 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17577596 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 16283 RMVar_ID_16283 Human_SNP_ID_342016146 A-to-I Human chr7 - 138404144 138404143 138404145 AAGTTAAACTAAAAAAAAAAAAAAAAAAAAAGACCGCTGTGACCTATTCACCCTCCACTTCCCGT AAGTTAAACTAAAAAAAAAAAAAAAAAAAAA__CCGCTGTGACCTATTCACCCTCCACTTCCCGT GTC G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1554422391 Functional Loss DEL dbSNP153 32..33 33 - - - 16284 RMVar_ID_16284 Human_SNP_ID_342016147 A-to-I Human chr7 - 138404144 138404144 138404144 AAGTTAAACTAAAAAAAAAAAAAAAAAAAAAGACCGCTGTGACCTATTCACCCTCCACTTCCCGT AAGTTAAACTAAAAAAAAAAAAAAAAAAAAAGGCCGCTGTGACCTATTCACCCTCCACTTCCCGT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs937576537 Functional Loss SNV dbSNP153 33..33 33 - - - 16285 RMVar_ID_16285 Human_SNP_ID_342112365 A-to-I Human chr7 - 138759198 138759198 138759198 AAAGTTAACCAAGTGTGGTGGCACACACCGGTAGTCCCAGCTACTTAGGAGGCTGAGGTGGGAGG AAAGTTAACCAAGTGTGGTGGCACACACCGGTTGTCCCAGCTACTTAGGAGGCTGAGGTGGGAGG T A ATP6V0A4 Ensembl:ENSG00000105929 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs951481564 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18737,RMVar_hsa_circ_10379,RMVar_hsa_circ_18677 16286 RMVar_ID_16286 Human_SNP_ID_342112366 A-to-I Human chr7 - 138759198 138759198 138759198 AAAGTTAACCAAGTGTGGTGGCACACACCGGTAGTCCCAGCTACTTAGGAGGCTGAGGTGGGAGG AAAGTTAACCAAGTGTGGTGGCACACACCGGTGGTCCCAGCTACTTAGGAGGCTGAGGTGGGAGG T C ATP6V0A4 Ensembl:ENSG00000105929 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs951481564 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18737,RMVar_hsa_circ_10379,RMVar_hsa_circ_18677 16287 RMVar_ID_16287 Human_SNP_ID_342181992 A-to-I Human chr7 - 139033114 139033114 139033114 GCCTCTGCCTCCTGAGTTCAAGTGATTCTCCCACCTCAGTCTCCTGAATAGTTGGGACTACAGGC GCCTCTGCCTCCTGAGTTCAAGTGATTCTCCCGCCTCAGTCTCCTGAATAGTTGGGACTACAGGC T C ZC3HAV1L Ensembl:ENSG00000146858 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs969177994 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_304246,RMVar_hsa_circ_248935,RMVar_hsa_circ_347000 16288 RMVar_ID_16288 Human_SNP_ID_342185897 A-to-I Human chr7 - 139048349 139048349 139048349 CACCCGCCTCAACCTCCCATAATGCTGGGATTACAGACATGAGCCACTGCACCTGCCCAGAGTAG CACCCGCCTCAACCTCCCATAATGCTGGGATTGCAGACATGAGCCACTGCACCTGCCCAGAGTAG T C ZC3HAV1 Ensembl:ENSG00000105939 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1011885324 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80839,RMVar_hsa_circ_248937 16289 RMVar_ID_16289 Human_SNP_ID_342185941 A-to-I Human chr7 - 139048594 139048594 139048594 TAGAAAATATTATTAGTATTTTTTGATACAGAATCTCACTCTGTTGCCCAGGCTGGAGTGCAGTG TAGAAAATATTATTAGTATTTTTTGATACAGAGTCTCACTCTGTTGCCCAGGCTGGAGTGCAGTG T C ZC3HAV1 Ensembl:ENSG00000105939 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11981663 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80839,RMVar_hsa_circ_248937 16290 RMVar_ID_16290 Human_SNP_ID_342186703 A-to-I Human chr7 - 139051710 139051710 139051710 TAATTAATTAAATGACTGTGGCCAGGCATGGTAGCTTAGACCTGTAATTCCTGTACTTTGGGAGG TAATTAATTAAATGACTGTGGCCAGGCATGGTGGCTTAGACCTGTAATTCCTGTACTTTGGGAGG T C ZC3HAV1 Ensembl:ENSG00000105939 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs894076034 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80839,RMVar_hsa_circ_248937 16291 RMVar_ID_16291 Human_SNP_ID_342187019 A-to-I Human chr7 - 139052808 139052808 139052808 CCTACAACTTCAGCCCCTCAAGTAACTGGGACAACAGGTGTGTGCCACCACATCCAGCTAATTTT CCTACAACTTCAGCCCCTCAAGTAACTGGGACGACAGGTGTGTGCCACCACATCCAGCTAATTTT T C ZC3HAV1 Ensembl:ENSG00000105939 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs913544481 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80839,RMVar_hsa_circ_248937 16292 RMVar_ID_16292 Human_SNP_ID_342187020 A-to-I Human chr7 - 139052808 139052808 139052808 CCTACAACTTCAGCCCCTCAAGTAACTGGGACAACAGGTGTGTGCCACCACATCCAGCTAATTTT CCTACAACTTCAGCCCCTCAAGTAACTGGGACCACAGGTGTGTGCCACCACATCCAGCTAATTTT T G ZC3HAV1 Ensembl:ENSG00000105939 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs913544481 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80839,RMVar_hsa_circ_248937 16293 RMVar_ID_16293 Human_SNP_ID_342187042 A-to-I Human chr7 - 139052882 139052882 139052882 GGGTCTCACTTTGTCACCCAGTTTGGGTGACAATCTCGGCTCACTGCAGCCTCAACCTCCTGGGC GGGTCTCACTTTGTCACCCAGTTTGGGTGACAGTCTCGGCTCACTGCAGCCTCAACCTCCTGGGC T C ZC3HAV1 Ensembl:ENSG00000105939 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1194159999 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80839,RMVar_hsa_circ_248937 16294 RMVar_ID_16294 Human_SNP_ID_342187989 A-to-I Human chr7 - 139056547 139056547 139056547 AACTTTTTAAAAAGTTAGACAGGTGTGGTGGTACACACTTGTGGTCCCAGCTACTCAAGAGGTTG AACTTTTTAAAAAGTTAGACAGGTGTGGTGGTGCACACTTGTGGTCCCAGCTACTCAAGAGGTTG T C ZC3HAV1 Ensembl:ENSG00000105939 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs942959719 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80839,RMVar_hsa_circ_123841,RMVar_hsa_circ_78777,RMVar_hsa_circ_360967,RMVar_hsa_circ_248937,RMVar_hsa_circ_347505,RMVar_hsa_circ_248938,RMVar_hsa_circ_65507,RMVar_hsa_circ_248939,RMVar_hsa_circ_330773 16295 RMVar_ID_16295 Human_SNP_ID_342188007 A-to-I Human chr7 - 139056626 139056626 139056626 AAGGCAGAAGGATTGCTTGAGCCCAGGAGTTTAAGACCAGCCTGGGCAACATGGTGAGTTGAGAC AAGGCAGAAGGATTGCTTGAGCCCAGGAGTTTGAGACCAGCCTGGGCAACATGGTGAGTTGAGAC T C ZC3HAV1 Ensembl:ENSG00000105939 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1421041075 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80839,RMVar_hsa_circ_123841,RMVar_hsa_circ_78777,RMVar_hsa_circ_360967,RMVar_hsa_circ_248937,RMVar_hsa_circ_347505,RMVar_hsa_circ_248938,RMVar_hsa_circ_65507,RMVar_hsa_circ_248939,RMVar_hsa_circ_330773 16296 RMVar_ID_16296 Human_SNP_ID_342188164 A-to-I Human chr7 - 139057327 139057327 139057327 TTTGAGAAAGAGTCTCACTCTGCATGCAGGTTAGAGTGCAGTGGTGTGATCATGGCTCACTGCAG TTTGAGAAAGAGTCTCACTCTGCATGCAGGTTGGAGTGCAGTGGTGTGATCATGGCTCACTGCAG T C ZC3HAV1 Ensembl:ENSG00000105939 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs777527079 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80839,RMVar_hsa_circ_123841,RMVar_hsa_circ_78777,RMVar_hsa_circ_360967,RMVar_hsa_circ_248937,RMVar_hsa_circ_347505,RMVar_hsa_circ_248938,RMVar_hsa_circ_65507,RMVar_hsa_circ_248939,RMVar_hsa_circ_330773 16297 RMVar_ID_16297 Human_SNP_ID_342188451 A-to-I Human chr7 - 139058322 139058322 139058322 AGTCACCCAAGTAACTAGGACTATGGGTGCACACCGCTACACCTGACTAATTTTTTTATTTTTTA AGTCACCCAAGTAACTAGGACTATGGGTGCACGCCGCTACACCTGACTAATTTTTTTATTTTTTA T C ZC3HAV1 Ensembl:ENSG00000105939 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1412319342 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80839,RMVar_hsa_circ_123841,RMVar_hsa_circ_78777,RMVar_hsa_circ_360967,RMVar_hsa_circ_248937,RMVar_hsa_circ_347505,RMVar_hsa_circ_248938,RMVar_hsa_circ_65507,RMVar_hsa_circ_248939,RMVar_hsa_circ_330773 16298 RMVar_ID_16298 Human_SNP_ID_342190686 A-to-I Human chr7 - 139067241 139067241 139067241 GGAGGCTGAGGCGGGAGAATTCGCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCCCAGATTGTG GGAGGCTGAGGCGGGAGAATTCGCTTGAACCCGGGAGGCGGAGGTTGCAGTGAGCCCAGATTGTG T C ZC3HAV1 Ensembl:ENSG00000105939 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1290906703 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 16299 RMVar_ID_16299 Human_SNP_ID_342190737 A-to-I Human chr7 - 139067437 139067437 139067437 GGTGAAATTTTGCTTCCCTGGCCAGGTGCAGTAGCTCATGCCTGCAATCCCAGCACTTTGGGAGG GGTGAAATTTTGCTTCCCTGGCCAGGTGCAGTTGCTCATGCCTGCAATCCCAGCACTTTGGGAGG T A ZC3HAV1 Ensembl:ENSG00000105939 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1347040874 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 16300 RMVar_ID_16300 Human_SNP_ID_342191712 A-to-I Human chr7 - 139071151 139071151 139071151 TAGGGGTTGCAGTGACCCGAGACTGTGCCACTACGCTCCAGCCTGGGTGACAGAGTAAGACTCCA TAGGGGTTGCAGTGACCCGAGACTGTGCCACTGCGCTCCAGCCTGGGTGACAGAGTAAGACTCCA T C ZC3HAV1 Ensembl:ENSG00000105939 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1048059613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26077387 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 16301 RMVar_ID_16301 Human_SNP_ID_342192218 A-to-I Human chr7 - 139073099 139073099 139073099 TAGACATGGGGTTTCAACATGTTGGACAGGCTAGTCGTGAACTCCTGACCTCAGGTTATCCGCCC TAGACATGGGGTTTCAACATGTTGGACAGGCTCGTCGTGAACTCCTGACCTCAGGTTATCCGCCC T G ZC3HAV1 Ensembl:ENSG00000105939 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1563130709 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 16302 RMVar_ID_16302 Human_SNP_ID_342192229 A-to-I Human chr7 - 139073133 139073133 139073133 CACCACCACACCCAGCTAATTTTTGTATTTTTAGTAGACATGGGGTTTCAACATGTTGGACAGGC CACCACCACACCCAGCTAATTTTTGTATTTTTGGTAGACATGGGGTTTCAACATGTTGGACAGGC T C ZC3HAV1 Ensembl:ENSG00000105939 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1388782548 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 16303 RMVar_ID_16303 Human_SNP_ID_342192242 A-to-I Human chr7 - 139073199 139073199 139073199 CATCTCCTGGGTTCAAGCGATCTTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCATGCA CATCTCCTGGGTTCAAGCGATCTTCCTGCCTCTGCCTCCCGAGTAGCTGGGATTACAGGCATGCA T A ZC3HAV1 Ensembl:ENSG00000105939 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1291591959 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 16304 RMVar_ID_16304 Human_SNP_ID_342192260 A-to-I Human chr7 - 139073260 139073260 139073260 AGTTTCACTCTTATCACCCATGCTGGAGTGCAATGGCGTTATCTTGGCTCACTGCAACCTCCATC AGTTTCACTCTTATCACCCATGCTGGAGTGCAGTGGCGTTATCTTGGCTCACTGCAACCTCCATC T C ZC3HAV1 Ensembl:ENSG00000105939 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs531587425 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 16305 RMVar_ID_16305 Human_SNP_ID_342196580 A-to-I Human chr7 - 139090200 139090200 139090200 ATGTTAACAAAGGGCCAGGTGTGGTAGCTCATACCTGTAATCCCAGCACTTTAGGAGGCTGAGGC ATGTTAACAAAGGGCCAGGTGTGGTAGCTCATGCCTGTAATCCCAGCACTTTAGGAGGCTGAGGC T C ZC3HAV1 Ensembl:ENSG00000105939 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs980847821 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117368,RMVar_hsa_circ_248949 16306 RMVar_ID_16306 Human_SNP_ID_342198240 A-to-I Human chr7 - 139096922 139096917 139096922 AGACATGTTGCCCCGGCTGGTCTTGAATTCCTAAGCTCAAGCTATCCACCCTCCTCAGCCTCCCA AGACATGTTGCCCCGGCTGGTCTTGAATTCCT_____CAAGCTATCCACCCTCCTCAGCCTCCCA GAGCTT G ZC3HAV1 Ensembl:ENSG00000105939 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1386057338 Functional Loss DEL dbSNP153 33..37 33 - - - RMVar_hsa_circ_117368,RMVar_hsa_circ_248949 16307 RMVar_ID_16307 Human_SNP_ID_342198240 A-to-I Human chr7 - 139096921 139096917 139096922 GACATGTTGCCCCGGCTGGTCTTGAATTCCTAAGCTCAAGCTATCCACCCTCCTCAGCCTCCCAA GACATGTTGCCCCGGCTGGTCTTGAATTCCT_____CAAGCTATCCACCCTCCTCAGCCTCCCAA GAGCTT G ZC3HAV1 Ensembl:ENSG00000105939 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1386057338 Functional Loss DEL dbSNP153 32..36 33 - - - RMVar_hsa_circ_117368,RMVar_hsa_circ_248949 16308 RMVar_ID_16308 Human_SNP_ID_342217929 A-to-I Human chr7 + 139177636 139177636 139177636 TATATATAGTGTGTGTGTGTGTGTGTGTATATATATCTCAAATGTACATAGTATATCAGACTGTG TATATATAGTGTGTGTGTGTGTGTGTGTATATGTATCTCAAATGTACATAGTATATCAGACTGTG A G TTC26 Ensembl:ENSG00000105948 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs989030935 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39780,RMVar_hsa_circ_341174,RMVar_hsa_circ_248956,RMVar_hsa_circ_346433,RMVar_hsa_circ_338535 16309 RMVar_ID_16309 Human_SNP_ID_342233848 A-to-I Human chr7 + 139241833 139241833 139241833 CCTGGCCAACATGGTGAAACCTTTCTATCTCTACTAAAAATACAAAAATTAGCTGGGCATGGTGG CCTGGCCAACATGGTGAAACCTTTCTATCTCTCCTAAAAATACAAAAATTAGCTGGGCATGGTGG A C UBN2 Ensembl:ENSG00000157741 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs558774237 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_248960,RMVar_hsa_circ_282412,RMVar_hsa_circ_301027,RMVar_hsa_circ_320742,RMVar_hsa_circ_355695,RMVar_hsa_circ_359338,RMVar_hsa_circ_352720,RMVar_hsa_circ_306807,RMVar_hsa_circ_290884,RMVar_hsa_circ_295684,RMVar_hsa_circ_283290,RMVar_hsa_circ_248964,RMVar_hsa_circ_33494,RMVar_hsa_circ_69290,RMVar_hsa_circ_248966,RMVar_hsa_circ_248967,RMVar_hsa_circ_248965,RMVar_hsa_circ_248962,RMVar_hsa_circ_248963,RMVar_hsa_circ_248961,RMVar_hsa_circ_248968 16310 RMVar_ID_16310 Human_SNP_ID_342245556 A-to-I Human chr7 + 139286175 139286174 139286175 ATCTTGAACTCCTGACCCCAGTTGATCTGCCCACCTCGGCCTCCCAAAGTGCTGGGCTTACAGGC ATCTTGAACTCCTGACCCCAGTTGATCTGCCC_CCTCGGCCTCCCAAAGTGCTGGGCTTACAGGC CA C UBN2 Ensembl:ENSG00000157741 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs764945220 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_16037413 RMVar_hsa_circ_33494,RMVar_hsa_circ_248967,RMVar_hsa_circ_54252,RMVar_hsa_circ_377711,RMVar_hsa_circ_248970,RMVar_hsa_circ_97761,RMVar_hsa_circ_248974,RMVar_hsa_circ_106684,RMVar_hsa_circ_248976,RMVar_hsa_circ_95412,RMVar_hsa_circ_248979,RMVar_hsa_circ_81037,RMVar_hsa_circ_248993,RMVar_hsa_circ_248995,RMVar_hsa_circ_89085 16311 RMVar_ID_16311 Human_SNP_ID_342246658 A-to-I Human chr7 + 139290170 139290170 139290170 GTTGGTCAGGCTGGTTTCGAATTCCTGATCTCATGATCCGCCCACCTTGGCCTCCCAAAGTGCTG GTTGGTCAGGCTGGTTTCGAATTCCTGATCTCGTGATCCGCCCACCTTGGCCTCCCAAAGTGCTG A G UBN2 Ensembl:ENSG00000157741 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs376350672 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33494,RMVar_hsa_circ_248967,RMVar_hsa_circ_54252,RMVar_hsa_circ_377711,RMVar_hsa_circ_248970,RMVar_hsa_circ_97761,RMVar_hsa_circ_248974,RMVar_hsa_circ_106684,RMVar_hsa_circ_248976,RMVar_hsa_circ_95412,RMVar_hsa_circ_248979,RMVar_hsa_circ_81037,RMVar_hsa_circ_248993,RMVar_hsa_circ_248995,RMVar_hsa_circ_89085 16312 RMVar_ID_16312 Human_SNP_ID_342265977 A-to-I Human chr7 + 139362843 139362843 139362843 CCCTTCCTGACAGTTTTTAATTAGTTCCTTTTAAAATTCATTGGAGATTTAAGTCTGTTAGTTAA CCCTTCCTGACAGTTTTTAATTAGTTCCTTTTGAAATTCATTGGAGATTTAAGTCTGTTAGTTAA A G FMC1-LUC7L2,LUC7L2 Ensembl:ENSG00000269955,Ensembl:ENSG00000146963 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs534424860 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34626 16313 RMVar_ID_16313 Human_SNP_ID_342267453 A-to-I Human chr7 + 139368591 139368591 139368591 TGAAACCTGTCTCTACTAAAAATATAAAAATTAGCCAGATGTGGTGGTGGGTGCCTGTAATCCCA TGAAACCTGTCTCTACTAAAAATATAAAAATTGGCCAGATGTGGTGGTGGGTGCCTGTAATCCCA A G FMC1-LUC7L2,LUC7L2 Ensembl:ENSG00000269955,Ensembl:ENSG00000146963 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10954645 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34626 16314 RMVar_ID_16314 Human_SNP_ID_342267454 A-to-I Human chr7 + 139368595 139368595 139368595 ACCTGTCTCTACTAAAAATATAAAAATTAGCCAGATGTGGTGGTGGGTGCCTGTAATCCCAGCCA ACCTGTCTCTACTAAAAATATAAAAATTAGCCGGATGTGGTGGTGGGTGCCTGTAATCCCAGCCA A G FMC1-LUC7L2,LUC7L2 Ensembl:ENSG00000269955,Ensembl:ENSG00000146963 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs938224289 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34626 16315 RMVar_ID_16315 Human_SNP_ID_342267471 A-to-I Human chr7 + 139368663 139368663 139368663 GGGAGGCTGAGGTTGGAGAATTGTTTGAACCCAGGAGACGGAGGTTGCTGTGAGCCCACATGGTG GGGAGGCTGAGGTTGGAGAATTGTTTGAACCCGGGAGACGGAGGTTGCTGTGAGCCCACATGGTG A G FMC1-LUC7L2,LUC7L2 Ensembl:ENSG00000269955,Ensembl:ENSG00000146963 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs898404273 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7703982,Human_RBP_ID_16038781 RMVar_hsa_circ_34626 16316 RMVar_ID_16316 Human_SNP_ID_342267951 A-to-I Human chr7 + 139370481 139370480 139370482 CACAAGGGTTTTTTGTTTGTTTGGTTTGAGACAGAGTCTTGCTCTGTGAGCCAGGCTGGAGTGCA CACAAGGGTTTTTTGTTTGTTTGGTTTGAGAC__AGTCTTGCTCTGTGAGCCAGGCTGGAGTGCA CAG C FMC1-LUC7L2,LUC7L2 Ensembl:ENSG00000269955,Ensembl:ENSG00000146963 Protein coding,Protein coding intron,intron GSE100210;GSE107867 HepG2 cell line;ASD brains,frontal_cortex - 29129909,30559470 RNA-Seq:(High) rs1388728974 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_7704038 RMVar_hsa_circ_34626 16317 RMVar_ID_16317 Human_SNP_ID_342267965 A-to-I Human chr7 + 139370551 139370551 139370551 GCTATCTCAGCTCACTGCAACCTCCAACTCCCAGGTTCAAGCGATTCTCCCACCCCAGCCTCTGT GCTATCTCAGCTCACTGCAACCTCCAACTCCCTGGTTCAAGCGATTCTCCCACCCCAGCCTCTGT A T FMC1-LUC7L2,LUC7L2 Ensembl:ENSG00000269955,Ensembl:ENSG00000146963 Protein coding,Protein coding intron,intron GSE38233;GSE107867 cultured B-cells;ASD brains,temporal_cortex - 24183664,30559470 RNA-Seq:(High) rs1211214311 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34626 16318 RMVar_ID_16318 Human_SNP_ID_342270098 A-to-I Human chr7 + 139379240 139379240 139379240 AGAATACAGAAAAGCCAGGCATGGTTGTACATACTTATAGCCCCAGCTACTTTGGAGGCTGAGGT AGAATACAGAAAAGCCAGGCATGGTTGTACATGCTTATAGCCCCAGCTACTTTGGAGGCTGAGGT A G FMC1-LUC7L2,LUC7L2 Ensembl:ENSG00000269955,Ensembl:ENSG00000146963 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1194183733 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_303,RMVar_hsa_circ_315992,RMVar_hsa_circ_348512,RMVar_hsa_circ_360883,RMVar_hsa_circ_362279,RMVar_hsa_circ_343796,RMVar_hsa_circ_45769,RMVar_hsa_circ_248999,RMVar_hsa_circ_249002,RMVar_hsa_circ_53454,RMVar_hsa_circ_330923,RMVar_hsa_circ_375522,RMVar_hsa_circ_359460,RMVar_hsa_circ_249003,RMVar_hsa_circ_59912,RMVar_hsa_circ_313326,RMVar_hsa_circ_21542 16319 RMVar_ID_16319 Human_SNP_ID_342270101 A-to-I Human chr7 + 139379246 139379246 139379246 CAGAAAAGCCAGGCATGGTTGTACATACTTATAGCCCCAGCTACTTTGGAGGCTGAGGTGGGAAG CAGAAAAGCCAGGCATGGTTGTACATACTTATGGCCCCAGCTACTTTGGAGGCTGAGGTGGGAAG A G FMC1-LUC7L2,LUC7L2 Ensembl:ENSG00000269955,Ensembl:ENSG00000146963 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1207488458 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_303,RMVar_hsa_circ_315992,RMVar_hsa_circ_348512,RMVar_hsa_circ_360883,RMVar_hsa_circ_362279,RMVar_hsa_circ_343796,RMVar_hsa_circ_45769,RMVar_hsa_circ_248999,RMVar_hsa_circ_249002,RMVar_hsa_circ_53454,RMVar_hsa_circ_330923,RMVar_hsa_circ_375522,RMVar_hsa_circ_359460,RMVar_hsa_circ_249003,RMVar_hsa_circ_59912,RMVar_hsa_circ_313326,RMVar_hsa_circ_21542 16320 RMVar_ID_16320 Human_SNP_ID_342273207 A-to-I Human chr7 + 139390054 139390054 139390054 ATGCACATGTACTTCTAGCTAGTGAGGAGACTAAAGTGGGAAGATCACTTAAGCCTAGGAATTCA ATGCACATGTACTTCTAGCTAGTGAGGAGACTGAAGTGGGAAGATCACTTAAGCCTAGGAATTCA A G FMC1-LUC7L2,LUC7L2 Ensembl:ENSG00000269955,Ensembl:ENSG00000146963 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1163657833 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17577623 RMVar_hsa_circ_303,RMVar_hsa_circ_315992,RMVar_hsa_circ_348512,RMVar_hsa_circ_360883,RMVar_hsa_circ_362279,RMVar_hsa_circ_343796,RMVar_hsa_circ_45769,RMVar_hsa_circ_248999,RMVar_hsa_circ_249002,RMVar_hsa_circ_53454,RMVar_hsa_circ_330923,RMVar_hsa_circ_375522,RMVar_hsa_circ_359460,RMVar_hsa_circ_249003,RMVar_hsa_circ_59912,RMVar_hsa_circ_313326,RMVar_hsa_circ_21542 16321 RMVar_ID_16321 Human_SNP_ID_342273212 A-to-I Human chr7 + 139390072 139390072 139390072 CTAGTGAGGAGACTAAAGTGGGAAGATCACTTAAGCCTAGGAATTCAAGGCCGCAGTGAGCTATG CTAGTGAGGAGACTAAAGTGGGAAGATCACTTGAGCCTAGGAATTCAAGGCCGCAGTGAGCTATG A G FMC1-LUC7L2,LUC7L2 Ensembl:ENSG00000269955,Ensembl:ENSG00000146963 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs979770560 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17577623 RMVar_hsa_circ_303,RMVar_hsa_circ_315992,RMVar_hsa_circ_348512,RMVar_hsa_circ_360883,RMVar_hsa_circ_362279,RMVar_hsa_circ_343796,RMVar_hsa_circ_45769,RMVar_hsa_circ_248999,RMVar_hsa_circ_249002,RMVar_hsa_circ_53454,RMVar_hsa_circ_330923,RMVar_hsa_circ_375522,RMVar_hsa_circ_359460,RMVar_hsa_circ_249003,RMVar_hsa_circ_59912,RMVar_hsa_circ_313326,RMVar_hsa_circ_21542 16322 RMVar_ID_16322 Human_SNP_ID_342274070 A-to-I Human chr7 + 139392888 139392888 139392888 GTTGGTCAGGCTGTTCTCAAACTCCCAACCTCAGGTGATCTGCCCGCCTCGGCCTCACAAAGTGC GTTGGTCAGGCTGTTCTCAAACTCCCAACCTCGGGTGATCTGCCCGCCTCGGCCTCACAAAGTGC A G FMC1-LUC7L2,LUC7L2 Ensembl:ENSG00000269955,Ensembl:ENSG00000146963 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1056472795 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_303,RMVar_hsa_circ_315992,RMVar_hsa_circ_348512,RMVar_hsa_circ_360883,RMVar_hsa_circ_362279,RMVar_hsa_circ_343796,RMVar_hsa_circ_45769,RMVar_hsa_circ_248999,RMVar_hsa_circ_249002,RMVar_hsa_circ_53454,RMVar_hsa_circ_330923,RMVar_hsa_circ_375522,RMVar_hsa_circ_359460,RMVar_hsa_circ_249003,RMVar_hsa_circ_59912,RMVar_hsa_circ_313326,RMVar_hsa_circ_21542 16323 RMVar_ID_16323 Human_SNP_ID_342274137 A-to-I Human chr7 + 139393080 139393080 139393080 CCTGAGGTGAAGAGTTTTAGACCAGCCAGGCCAACATGATGAAACCCCAACTCTACTAAAAATAC CCTGAGGTGAAGAGTTTTAGACCAGCCAGGCCGACATGATGAAACCCCAACTCTACTAAAAATAC A G FMC1-LUC7L2,LUC7L2 Ensembl:ENSG00000269955,Ensembl:ENSG00000146963 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1489119642 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_303,RMVar_hsa_circ_315992,RMVar_hsa_circ_348512,RMVar_hsa_circ_360883,RMVar_hsa_circ_362279,RMVar_hsa_circ_343796,RMVar_hsa_circ_45769,RMVar_hsa_circ_248999,RMVar_hsa_circ_249002,RMVar_hsa_circ_53454,RMVar_hsa_circ_330923,RMVar_hsa_circ_375522,RMVar_hsa_circ_359460,RMVar_hsa_circ_249003,RMVar_hsa_circ_59912,RMVar_hsa_circ_313326,RMVar_hsa_circ_21542 16324 RMVar_ID_16324 Human_SNP_ID_342274151 A-to-I Human chr7 + 139393124 139393124 139393124 CCCCAACTCTACTAAAAATACAAAAATTAGCCAGGTGTGGTGGTGCACACTTGTAATCCCAGCTA CCCCAACTCTACTAAAAATACAAAAATTAGCCTGGTGTGGTGGTGCACACTTGTAATCCCAGCTA A T FMC1-LUC7L2,LUC7L2 Ensembl:ENSG00000269955,Ensembl:ENSG00000146963 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs74856652 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_303,RMVar_hsa_circ_315992,RMVar_hsa_circ_348512,RMVar_hsa_circ_360883,RMVar_hsa_circ_362279,RMVar_hsa_circ_343796,RMVar_hsa_circ_45769,RMVar_hsa_circ_248999,RMVar_hsa_circ_249002,RMVar_hsa_circ_53454,RMVar_hsa_circ_330923,RMVar_hsa_circ_375522,RMVar_hsa_circ_359460,RMVar_hsa_circ_249003,RMVar_hsa_circ_59912,RMVar_hsa_circ_313326,RMVar_hsa_circ_21542 16325 RMVar_ID_16325 Human_SNP_ID_342277437 A-to-I Human chr7 + 139405750 139405750 139405750 GAATGTGGAGGAATCCCAGAAAGTAATGGATGAAGTAGAGAAAGCACGGGCAAAGAAAAGAGAAG GAATGTGGAGGAATCCCAGAAAGTAATGGATGGAGTAGAGAAAGCACGGGCAAAGAAAAGAGAAG A G FMC1-LUC7L2,LUC7L2 Ensembl:ENSG00000269955,Ensembl:ENSG00000146963 Protein coding,Protein coding CDS,CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928827416 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1682475,Human_RBP_ID_2036430,Human_RBP_ID_3834868,Human_RBP_ID_5628239,Human_RBP_ID_7704422,Human_RBP_ID_16040432,Human_RBP_ID_18876988,Human_RBP_ID_22833537,Human_RBP_ID_23081140,Human_RBP_ID_24195371,Human_RBP_ID_24549039,Human_RBP_ID_27830892 Human_Splice_Rec_928361,Human_Splice_Rec_928391,Human_Splice_Rec_928409,Human_Splice_Rec_928431,Human_Splice_Rec_928449,Human_Splice_Rec_928465,Human_Splice_Rec_928477,Human_Splice_Rec_928499 RMVar_hsa_circ_303,RMVar_hsa_circ_315992,RMVar_hsa_circ_348512,RMVar_hsa_circ_362279,RMVar_hsa_circ_343796,RMVar_hsa_circ_248999,RMVar_hsa_circ_53454,RMVar_hsa_circ_375522,RMVar_hsa_circ_249003,RMVar_hsa_circ_313326,RMVar_hsa_circ_64938,RMVar_hsa_circ_249006,RMVar_hsa_circ_283814,RMVar_hsa_circ_302643,RMVar_hsa_circ_326668,RMVar_hsa_circ_301556,RMVar_hsa_circ_249008,RMVar_hsa_circ_280276,RMVar_hsa_circ_249007,RMVar_hsa_circ_249005,RMVar_hsa_circ_310774,RMVar_hsa_circ_351222,RMVar_hsa_circ_368749,RMVar_hsa_circ_310971,RMVar_hsa_circ_102933,RMVar_hsa_circ_38595,RMVar_hsa_circ_249009,RMVar_hsa_circ_249011,RMVar_hsa_circ_249012,RMVar_hsa_circ_249010,RMVar_hsa_circ_55037 16326 RMVar_ID_16326 Human_SNP_ID_342279733 A-to-I Human chr7 + 139413553 139413552 139413553 CCATCACAGCTCTTTGGGAGGCCGAGGCAGCCAGATCACCTGAAGTCAGGAGTTCGAGACCAGCC CCATCACAGCTCTTTGGGAGGCCGAGGCAGCC_GATCACCTGAAGTCAGGAGTTCGAGACCAGCC CA C FMC1-LUC7L2,LUC7L2 Ensembl:ENSG00000269955,Ensembl:ENSG00000146963 Protein coding,Protein coding intron,intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1051438228 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_348512,RMVar_hsa_circ_375522,RMVar_hsa_circ_249003,RMVar_hsa_circ_313326,RMVar_hsa_circ_64938,RMVar_hsa_circ_301556,RMVar_hsa_circ_249008,RMVar_hsa_circ_102933,RMVar_hsa_circ_38595,RMVar_hsa_circ_249012,RMVar_hsa_circ_345718,RMVar_hsa_circ_1191 16327 RMVar_ID_16327 Human_SNP_ID_342281266 A-to-I Human chr7 + 139418972 139418972 139418972 CATCTCTACTAAAATACAAACATTAGCCGGGCATGGTGGCACATGCCTGTAATCCCAGCTACTCA CATCTCTACTAAAATACAAACATTAGCCGGGCGTGGTGGCACATGCCTGTAATCCCAGCTACTCA A G FMC1-LUC7L2,LUC7L2 Ensembl:ENSG00000269955,Ensembl:ENSG00000146963 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1326584154 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102933,RMVar_hsa_circ_249012 16328 RMVar_ID_16328 Human_SNP_ID_342281276 A-to-I Human chr7 + 139419004 139419004 139419004 ATGGTGGCACATGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGAAGGAGAATTGCTTGAACACA ATGGTGGCACATGCCTGTAATCCCAGCTACTCCGGAGGCTGAGGAAGGAGAATTGCTTGAACACA A C FMC1-LUC7L2,LUC7L2 Ensembl:ENSG00000269955,Ensembl:ENSG00000146963 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1186886569 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16040944 RMVar_hsa_circ_102933,RMVar_hsa_circ_249012 16329 RMVar_ID_16329 Human_SNP_ID_342281692 A-to-I Human chr7 + 139420361 139420361 139420361 AAGTAGCTGGGATTACAGGCCCAGGCCACCACACCTGGCTATTTTTGTATTTTTAGTAGGGACAG AAGTAGCTGGGATTACAGGCCCAGGCCACCACGCCTGGCTATTTTTGTATTTTTAGTAGGGACAG A G FMC1-LUC7L2,LUC7L2 Ensembl:ENSG00000269955,Ensembl:ENSG00000146963 Protein coding,Protein coding intron,intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs543460113 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_676966,Human_RBP_ID_16041022,Human_RBP_ID_17712407,Human_RBP_ID_18093943 RMVar_hsa_circ_102933,RMVar_hsa_circ_249012 16330 RMVar_ID_16330 Human_SNP_ID_342283354 A-to-I Human chr7 + 139425922 139425922 139425922 TAAGGCACGAGAATCGTTTGAACCCGGGAGGCAGAGGCTGCAGTGAGCCGAGATCGCACTCCAGT TAAGGCACGAGAATCGTTTGAACCCGGGAGGCTGAGGCTGCAGTGAGCCGAGATCGCACTCCAGT A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1000767300 Functional Loss SNV dbSNP153 33..33 33 - - - 16331 RMVar_ID_16331 Human_SNP_ID_342283470 A-to-I Human chr7 + 139426191 139426191 139426191 AAAAAAAAATTGTAGAGATGGAGTCTTGCTTTATTGCCCAGGCTGGTCTACAACTCCTGGGCTCA AAAAAAAAATTGTAGAGATGGAGTCTTGCTTTCTTGCCCAGGCTGGTCTACAACTCCTGGGCTCA A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1207902391 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16041291 16332 RMVar_ID_16332 Human_SNP_ID_342312912 A-to-I Human chr7 + 139534262 139534262 139534262 AGTTTGGCGCGATGTCTCACACCATTTTGCTGATACAGACTACCAAGAGGCCAGAAGGCAGAACT AGTTTGGCGCGATGTCTCACACCATTTTGCTGGTACAGACTACCAAGAGGCCAGAAGGCAGAACT A G CLEC2L,ERHP1 Ensembl:ENSG00000236279,Ensembl:ENSG00000254270 Protein coding,Pseudogene intron,exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs879035410 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1893793 16333 RMVar_ID_16333 Human_SNP_ID_342324735 A-to-I Human chr7 - 139581092 139581092 139581092 TCTCAGCCTCCCAAATAGCTGGGACTACCGGCATGCACCACCACGCCCGGCTAACTTTTTGTATT TCTCAGCCTCCCAAATAGCTGGGACTACCGGCGTGCACCACCACGCCCGGCTAACTTTTTGTATT T C HIPK2 Ensembl:ENSG00000064393 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1259502558 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267067,RMVar_hsa_circ_376739,RMVar_hsa_circ_249016 16334 RMVar_ID_16334 Human_SNP_ID_342324738 A-to-I Human chr7 - 139581098 139581098 139581098 CTGCTGTCTCAGCCTCCCAAATAGCTGGGACTACCGGCATGCACCACCACGCCCGGCTAACTTTT CTGCTGTCTCAGCCTCCCAAATAGCTGGGACTGCCGGCATGCACCACCACGCCCGGCTAACTTTT T C HIPK2 Ensembl:ENSG00000064393 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1027545968 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267067,RMVar_hsa_circ_376739,RMVar_hsa_circ_249016 16335 RMVar_ID_16335 Human_SNP_ID_342324747 A-to-I Human chr7 - 139581133 139581133 139581133 TTACTGCAACCTCTACTTCCCGGGTTCAAGCAATTCTGCTGTCTCAGCCTCCCAAATAGCTGGGA TTACTGCAACCTCTACTTCCCGGGTTCAAGCAGTTCTGCTGTCTCAGCCTCCCAAATAGCTGGGA T C HIPK2 Ensembl:ENSG00000064393 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1479285658 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267067,RMVar_hsa_circ_376739,RMVar_hsa_circ_249016 16336 RMVar_ID_16336 Human_SNP_ID_342338639 A-to-I Human chr7 - 139640717 139640717 139640717 TGAGCCCAGGAGGTGGAAGGTGCGGTCAACCAAGATTGTGCCACTGCACTCCAGCCTGGACAACA TGAGCCCAGGAGGTGGAAGGTGCGGTCAACCAGGATTGTGCCACTGCACTCCAGCCTGGACAACA T C HIPK2 Ensembl:ENSG00000064393 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs115566818 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56255 16337 RMVar_ID_16337 Human_SNP_ID_342338661 A-to-I Human chr7 - 139640842 139640839 139640842 GGAGGCTGAAGCGGAAGGATTGCTTGAGCTCAAGAGCTCAAGAAGAGCCTGGGCAACATGGTGAA GGAGGCTGAAGCGGAAGGATTGCTTGAGCTCA___GCTCAAGAAGAGCCTGGGCAACATGGTGAA CTCT C HIPK2 Ensembl:ENSG00000064393 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1467956217 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_56255 16338 RMVar_ID_16338 Human_SNP_ID_342344524 A-to-I Human chr7 - 139664498 139664498 139664498 CAGTCTCACTGTGTTGCCCCGGCTGGAGTGCAATGGCTTGATCTCGGCTCACTGTAAACTCTGCC CAGTCTCACTGTGTTGCCCCGGCTGGAGTGCAGTGGCTTGATCTCGGCTCACTGTAAACTCTGCC T C HIPK2 Ensembl:ENSG00000064393 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1332004429 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56255 16339 RMVar_ID_16339 Human_SNP_ID_342349682 A-to-I Human chr7 - 139684601 139684601 139684601 GTGATTCTCCTGCATCCAGAGTACCTAGGACTATAGGTACACATCACTATGTCCAGCTAATTTTT GTGATTCTCCTGCATCCAGAGTACCTAGGACTCTAGGTACACATCACTATGTCCAGCTAATTTTT T G HIPK2 Ensembl:ENSG00000064393 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs146112122 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56255 16340 RMVar_ID_16340 Human_SNP_ID_342359941 A-to-I Human chr7 - 139728077 139728077 139728077 AAATTAGGCAGGCATGATGGCGCACACCTGTAATCCCAGCTACTTGGGAGACTGAGGTGGGAGGA AAATTAGGCAGGCATGATGGCGCACACCTGTAGTCCCAGCTACTTGGGAGACTGAGGTGGGAGGA T C HIPK2 Ensembl:ENSG00000064393 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1213068343 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92512,RMVar_hsa_circ_249027 16341 RMVar_ID_16341 Human_SNP_ID_342359952 A-to-I Human chr7 - 139728104 139728104 139728104 ACCCCGTCTCTATAAAAAAATAAAAATAAATTAGGCAGGCATGATGGCGCACACCTGTAATCCCA ACCCCGTCTCTATAAAAAAATAAAAATAAATTGGGCAGGCATGATGGCGCACACCTGTAATCCCA T C HIPK2 Ensembl:ENSG00000064393 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs922471284 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92512,RMVar_hsa_circ_249027 16342 RMVar_ID_16342 Human_SNP_ID_342433307 A-to-I Human chr7 - 140031367 140031367 140031367 TATGTATTTATTTATTTATTTATTTATGAGACAGGGTCTCACTCTGTCACCCAGGATGGAATGCA TATGTATTTATTTATTTATTTATTTATGAGACTGGGTCTCACTCTGTCACCCAGGATGGAATGCA T A PARP12 Ensembl:ENSG00000059378 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs921346227 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16042897 RMVar_hsa_circ_249029,RMVar_hsa_circ_269671,RMVar_hsa_circ_376581,RMVar_hsa_circ_269037,RMVar_hsa_circ_371923 16343 RMVar_ID_16343 Human_SNP_ID_342464566 A-to-I Human chr7 - 140153039 140153039 140153039 CCTGGCCAACATGATGAAACCCTGTCTCTACTAAAAATACAAAAATTAGCTGGGTGTGGTGGCGC CCTGGCCAACATGATGAAACCCTGTCTCTACTGAAAATACAAAAATTAGCTGGGTGTGGTGGCGC T C KDM7A Ensembl:ENSG00000006459 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs904261392 Functional Loss SNV dbSNP153 33..33 33 - - - 16344 RMVar_ID_16344 Human_SNP_ID_342522625 A-to-I Human chr7 - 140386771 140386771 140386771 GGGAATACCGGGTGCTGTAGGCTTTAAAAAATAAAAATTCACCGATTGAGAAAATACTAAATGAC GGGAATACCGGGTGCTGTAGGCTTTAAAAAATGAAAATTCACCGATTGAGAAAATACTAAATGAC T C SLC37A3 Ensembl:ENSG00000157800 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1271604049 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14598,Human_RBP_ID_270994,Human_RBP_ID_1143529,Human_RBP_ID_1220154,Human_RBP_ID_1246965,Human_RBP_ID_1330635,Human_RBP_ID_1691425,Human_RBP_ID_3835236,Human_RBP_ID_4956716,Human_RBP_ID_5223184,Human_RBP_ID_5277223,Human_RBP_ID_5429893,Human_RBP_ID_5452822,Human_RBP_ID_5480394,Human_RBP_ID_5513938,Human_RBP_ID_7705915,Human_RBP_ID_8151256,Human_RBP_ID_8660125,Human_RBP_ID_8915561,Human_RBP_ID_9217853,Human_RBP_ID_9263204,Human_RBP_ID_9310315,Human_RBP_ID_16279987,Human_RBP_ID_17051323,Human_RBP_ID_17312039,Human_RBP_ID_17712447,Human_RBP_ID_18094268,Human_RBP_ID_18203042,Human_RBP_ID_18211499,Human_RBP_ID_18451240,Human_RBP_ID_18877224,Human_RBP_ID_19032908,Human_RBP_ID_21904228,Human_RBP_ID_21950541,Human_RBP_ID_22011567,Human_RBP_ID_22407232,Human_RBP_ID_22835925,Human_RBP_ID_23073097,Human_RBP_ID_23140377,Human_RBP_ID_23297770,Human_RBP_ID_23315711,Human_RBP_ID_24388899,Human_RBP_ID_26079068,Human_RBP_ID_26544503,Human_RBP_ID_26722542,Human_RBP_ID_26751884,Human_RBP_ID_27106337,Human_RBP_ID_27161770,Human_RBP_ID_27352777,Human_RBP_ID_27534831,Human_RBP_ID_27765108 RMVar_hsa_circ_269083 16345 RMVar_ID_16345 Human_SNP_ID_342541078 A-to-I Human chr7 - 140454731 140454731 140454731 AGTGCCATCCCTATCATGGCCTTGTTTTTTACAGGCCCAACGAAGGAACCACTTCTGGGAACTCA AGTGCCATCCCTATCATGGCCTTGTTTTTTACGGGCCCAACGAAGGAACCACTTCTGGGAACTCA T C MKRN1 Ensembl:ENSG00000133606 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_955015 16346 RMVar_ID_16346 Human_SNP_ID_342541079 A-to-I Human chr7 - 140454731 140454731 140454731 AGTGCCATCCCTATCATGGCCTTGTTTTTTACAGGCCCAACGAAGGAACCACTTCTGGGAACTCA AGTGCCATCCCTATCATGGCCTTGTTTTTTACCGGCCCAACGAAGGAACCACTTCTGGGAACTCA T G MKRN1 Ensembl:ENSG00000133606 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_955015 16347 RMVar_ID_16347 Human_SNP_ID_342542646 A-to-I Human chr7 - 140460152 140460152 140460152 ACCTCTGTCTCCTGGGTTCAAGTGATTCTCCTACCTCAGCCTCCCGAGTAGTTGGGATTACAGGT ACCTCTGTCTCCTGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGTTGGGATTACAGGT T C MKRN1 Ensembl:ENSG00000133606 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs752768755 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_929538,Human_Splice_Rec_929539 RMVar_hsa_circ_51329,RMVar_hsa_circ_249089,RMVar_hsa_circ_331662 16348 RMVar_ID_16348 Human_SNP_ID_342542647 A-to-I Human chr7 - 140460152 140460152 140460152 ACCTCTGTCTCCTGGGTTCAAGTGATTCTCCTACCTCAGCCTCCCGAGTAGTTGGGATTACAGGT ACCTCTGTCTCCTGGGTTCAAGTGATTCTCCTCCCTCAGCCTCCCGAGTAGTTGGGATTACAGGT T G MKRN1 Ensembl:ENSG00000133606 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs752768755 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_929538,Human_Splice_Rec_929539 RMVar_hsa_circ_51329,RMVar_hsa_circ_249089,RMVar_hsa_circ_331662 16349 RMVar_ID_16349 Human_SNP_ID_342542819 A-to-I Human chr7 - 140460580 140460580 140460580 TTAGGAATATATGGCCGTACGTGGTGGCTCACACCTGTAACCCCAGCACTTTGGGAGGCTGAGGT TTAGGAATATATGGCCGTACGTGGTGGCTCACGCCTGTAACCCCAGCACTTTGGGAGGCTGAGGT T C MKRN1 Ensembl:ENSG00000133606 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs545678938 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22687460 RMVar_hsa_circ_51329,RMVar_hsa_circ_249089,RMVar_hsa_circ_331662 16350 RMVar_ID_16350 Human_SNP_ID_342542820 A-to-I Human chr7 - 140460580 140460580 140460580 TTAGGAATATATGGCCGTACGTGGTGGCTCACACCTGTAACCCCAGCACTTTGGGAGGCTGAGGT TTAGGAATATATGGCCGTACGTGGTGGCTCACCCCTGTAACCCCAGCACTTTGGGAGGCTGAGGT T G MKRN1 Ensembl:ENSG00000133606 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs545678938 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22687460 RMVar_hsa_circ_51329,RMVar_hsa_circ_249089,RMVar_hsa_circ_331662 16351 RMVar_ID_16351 Human_SNP_ID_342544359 A-to-I Human chr7 - 140465959 140465959 140465959 CCGGTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCGCGCACCACCATGCCCAGCTAATTTTT CCGGTGCCTCAGCCTCCTGAGTAGCTGGGACTCCAGGCGCGCACCACCATGCCCAGCTAATTTTT T G MKRN1 Ensembl:ENSG00000133606 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1272337919 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51329,RMVar_hsa_circ_249089,RMVar_hsa_circ_331662 16352 RMVar_ID_16352 Human_SNP_ID_342544363 A-to-I Human chr7 - 140465981 140465981 140465981 CGCCTCCTGGGTTCAAGCGATTCCGGTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCGCGCA CGCCTCCTGGGTTCAAGCGATTCCGGTGCCTCGGCCTCCTGAGTAGCTGGGACTACAGGCGCGCA T C MKRN1 Ensembl:ENSG00000133606 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs909060399 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16044950 RMVar_hsa_circ_51329,RMVar_hsa_circ_249089,RMVar_hsa_circ_331662 16353 RMVar_ID_16353 Human_SNP_ID_342544377 A-to-I Human chr7 - 140466023 140466023 140466023 AGGCTGGAGTGCAGTGGCGTGATCTCGGCTCAATGCAATGTCCGCCTCCTGGGTTCAAGCGATTC AGGCTGGAGTGCAGTGGCGTGATCTCGGCTCAGTGCAATGTCCGCCTCCTGGGTTCAAGCGATTC T C MKRN1 Ensembl:ENSG00000133606 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs148889998 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51329,RMVar_hsa_circ_249089,RMVar_hsa_circ_331662 16354 RMVar_ID_16354 Human_SNP_ID_342545359 A-to-I Human chr7 - 140469137 140469137 140469137 TATTTTTAGTATAGACGGGGTTTCACTGTGTTAGCCAGGGTGGTCTTGATCTCCTGACCTCGTGA TATTTTTAGTATAGACGGGGTTTCACTGTGTTCGCCAGGGTGGTCTTGATCTCCTGACCTCGTGA T G MKRN1 Ensembl:ENSG00000133606 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1255997243 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51329,RMVar_hsa_circ_249089,RMVar_hsa_circ_331662 16355 RMVar_ID_16355 Human_SNP_ID_342545576 A-to-I Human chr7 - 140469814 140469814 140469814 GATCTCCTGACCAGCCCACACCAGCCTCCCAAAGTGCTGGGATTGTAGGCATGAGCCACCGCGCC GATCTCCTGACCAGCCCACACCAGCCTCCCAAGGTGCTGGGATTGTAGGCATGAGCCACCGCGCC T C MKRN1 Ensembl:ENSG00000133606 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1465754154 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51329,RMVar_hsa_circ_249089,RMVar_hsa_circ_331662 16356 RMVar_ID_16356 Human_SNP_ID_342546037 A-to-I Human chr7 - 140471181 140471181 140471181 GGGGGTCTTAATATGTTGCGTAGGCTGGTCTCAGATTCCTGGGCTCAAGCAATCTTCCTGCCTTG GGGGGTCTTAATATGTTGCGTAGGCTGGTCTCGGATTCCTGGGCTCAAGCAATCTTCCTGCCTTG T C MKRN1 Ensembl:ENSG00000133606 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1208168710 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17577983,Human_RBP_ID_26079140 RMVar_hsa_circ_51329,RMVar_hsa_circ_249089,RMVar_hsa_circ_331662 16357 RMVar_ID_16357 Human_SNP_ID_342546190 A-to-I Human chr7 - 140471745 140471745 140471745 AATGACTCTTGGCTGGGCAGTGGCTCATGCCTATAATCCCAGCACTTTGGGATGCTTAGGTAGGA AATGACTCTTGGCTGGGCAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGATGCTTAGGTAGGA T C MKRN1 Ensembl:ENSG00000133606 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559249045 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26079147 RMVar_hsa_circ_51329,RMVar_hsa_circ_249089,RMVar_hsa_circ_331662 16358 RMVar_ID_16358 Human_SNP_ID_342546878 A-to-I Human chr7 - 140473771 140473771 140473771 TCAGGCTGGTCTCAAACTCCCAACCTCAGGTAATCCACCCGCCTTGGCCTCCCAAAGTGCTGGGA TCAGGCTGGTCTCAAACTCCCAACCTCAGGTAGTCCACCCGCCTTGGCCTCCCAAAGTGCTGGGA T C MKRN1 Ensembl:ENSG00000133606 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1222163662 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_929476,Human_Splice_Rec_929520 RMVar_hsa_circ_295560 16359 RMVar_ID_16359 Human_SNP_ID_342546879 A-to-I Human chr7 - 140473771 140473771 140473771 TCAGGCTGGTCTCAAACTCCCAACCTCAGGTAATCCACCCGCCTTGGCCTCCCAAAGTGCTGGGA TCAGGCTGGTCTCAAACTCCCAACCTCAGGTACTCCACCCGCCTTGGCCTCCCAAAGTGCTGGGA T G MKRN1 Ensembl:ENSG00000133606 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1222163662 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_929476,Human_Splice_Rec_929520 RMVar_hsa_circ_295560 16360 RMVar_ID_16360 Human_SNP_ID_342547736 A-to-I Human chr7 - 140475595 140475595 140475595 CAGTGGCAGTGTCTTGGCTCATTGCAGCCTCCACCTCCCAGGCTCAAGCAATCCTCCTGCTTGAA CAGTGGCAGTGTCTTGGCTCATTGCAGCCTCCTCCTCCCAGGCTCAAGCAATCCTCCTGCTTGAA T A MKRN1 Ensembl:ENSG00000133606 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1253557761 Functional Loss SNV dbSNP153 33..33 33 - - - 16361 RMVar_ID_16361 Human_SNP_ID_342549468 A-to-I Human chr7 + 140480637 140480637 140480637 AAAATTAGCCGGTCATGATGGCGGGCGCCTGTAGTCCCAGCTACTCCGAGGCTGAGGCAGGAGAA AAAATTAGCCGGTCATGATGGCGGGCGCCTGTCGTCCCAGCTACTCCGAGGCTGAGGCAGGAGAA A C RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs925506918 Functional Loss SNV dbSNP153 33..33 33 - - - 16362 RMVar_ID_16362 Human_SNP_ID_342549469 A-to-I Human chr7 + 140480637 140480637 140480637 AAAATTAGCCGGTCATGATGGCGGGCGCCTGTAGTCCCAGCTACTCCGAGGCTGAGGCAGGAGAA AAAATTAGCCGGTCATGATGGCGGGCGCCTGTGGTCCCAGCTACTCCGAGGCTGAGGCAGGAGAA A G RF00017-4520 RNACentral:URS000099C2D3 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs925506918 Functional Loss SNV dbSNP153 33..33 33 - - - 16363 RMVar_ID_16363 Human_SNP_ID_342587971 A-to-I Human chr7 - 140628678 140628677 140628678 AAAATTGGCCGGGCGTGGTGGCGCATGCCTGTAGTTCCAGCTACTAGGGAGGCTGAGGCAGGAGA AAAATTGGCCGGGCGTGGTGGCGCATGCCTGT_GTTCCAGCTACTAGGGAGGCTGAGGCAGGAGA CT C DENND2A Ensembl:ENSG00000146966 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1402020340 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_84102,RMVar_hsa_circ_249102 16364 RMVar_ID_16364 Human_SNP_ID_342606020 A-to-I Human chr7 + 140700253 140700253 140700253 TCAAGTGATTCTCCTGCTTCAGCCTCCTGAGTAGCTGGGATTACATGCATGTACCACCATGCCCA TCAAGTGATTCTCCTGCTTCAGCCTCCTGAGTGGCTGGGATTACATGCATGTACCACCATGCCCA A G NDUFB2 Ensembl:ENSG00000090266 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1403600660 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87677,RMVar_hsa_circ_116814,RMVar_hsa_circ_249116,RMVar_hsa_circ_103384,RMVar_hsa_circ_249115,RMVar_hsa_circ_249117 16365 RMVar_ID_16365 Human_SNP_ID_342613308 A-to-I Human chr7 - 140729111 140729111 140729111 CCCACTTCAGCCTCCTCTAGGTAGCTAGGACTACATGCATGTGCCACCACATCCAACTGATTTTT CCCACTTCAGCCTCCTCTAGGTAGCTAGGACTTCATGCATGTGCCACCACATCCAACTGATTTTT T A BRAF Ensembl:ENSG00000157764 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1478654270 Functional Loss SNV dbSNP153 33..33 33 - - - 16366 RMVar_ID_16366 Human_SNP_ID_342613325 A-to-I Human chr7 - 140729188 140729188 140729188 TTTCGTTACTCAGGCTGGAGTGCAGTGGTACAATCCTGGCTCACTGCAGCCTCAACCTGCTGGTC TTTCGTTACTCAGGCTGGAGTGCAGTGGTACAGTCCTGGCTCACTGCAGCCTCAACCTGCTGGTC T C BRAF Ensembl:ENSG00000157764 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs374102458 Functional Loss SNV dbSNP153 33..33 33 - - - 16367 RMVar_ID_16367 Human_SNP_ID_342613764 A-to-I Human chr7 - 140731051 140731051 140731051 CATCATGCCACTGCACTCCAGCCTGGGCAACAAAGCAAAACCCTGTCTCAAAAAAAGAAAAGAAA CATCATGCCACTGCACTCCAGCCTGGGCAACAGAGCAAAACCCTGTCTCAAAAAAAGAAAAGAAA T C BRAF Ensembl:ENSG00000157764 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs934993023 Functional Loss SNV dbSNP153 33..33 33 - - - 16368 RMVar_ID_16368 Human_SNP_ID_342613828 A-to-I Human chr7 - 140731268 140731268 140731268 CTCACGCTGTAATCCCAGCACTTTTGGAGGCCAAGGTGGGCAGATCGCGTGAGCCCAGGAGTTTG CTCACGCTGTAATCCCAGCACTTTTGGAGGCCGAGGTGGGCAGATCGCGTGAGCCCAGGAGTTTG T C BRAF Ensembl:ENSG00000157764 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs534064395 Functional Loss SNV dbSNP153 33..33 33 - - - 16369 RMVar_ID_16369 Human_SNP_ID_342615362 A-to-I Human chr7 - 140736967 140736967 140736967 TAGCCCACTGCAGCCTCAAACTCCTGGGCTCAAGCGATCCTCTCACCTCAGCCTCCTAAGTAGCT TAGCCCACTGCAGCCTCAAACTCCTGGGCTCAGGCGATCCTCTCACCTCAGCCTCCTAAGTAGCT T C BRAF Ensembl:ENSG00000157764 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1195288548 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_249126,RMVar_hsa_circ_249124,RMVar_hsa_circ_121150,RMVar_hsa_circ_378566,RMVar_hsa_circ_305122,RMVar_hsa_circ_249123,RMVar_hsa_circ_378886,RMVar_hsa_circ_297428,RMVar_hsa_circ_249125 16370 RMVar_ID_16370 Human_SNP_ID_342615740 A-to-I Human chr7 - 140738762 140738762 140738762 AAATACAAAAATTAGCTGGGCATAGTGGCAGGAGCCTGTAATCCCAGCCACTCAGGAGGCTGAGA AAATACAAAAATTAGCTGGGCATAGTGGCAGGGGCCTGTAATCCCAGCCACTCAGGAGGCTGAGA T C BRAF Ensembl:ENSG00000157764 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1430047650 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_249126,RMVar_hsa_circ_249124,RMVar_hsa_circ_121150,RMVar_hsa_circ_378566,RMVar_hsa_circ_305122,RMVar_hsa_circ_249123,RMVar_hsa_circ_378886,RMVar_hsa_circ_297428,RMVar_hsa_circ_249125 16371 RMVar_ID_16371 Human_SNP_ID_342624835 A-to-I Human chr7 - 140774592 140774592 140774592 GGATCACTTGAGCCCAGGAGTGTGAGGATGCAAGGAGTCGTGATTGTGCCACTGCATCCAGCCTG GGATCACTTGAGCCCAGGAGTGTGAGGATGCAGGGAGTCGTGATTGTGCCACTGCATCCAGCCTG T C BRAF Ensembl:ENSG00000157764 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1163597643 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79167,RMVar_hsa_circ_42798,RMVar_hsa_circ_249126,RMVar_hsa_circ_249124,RMVar_hsa_circ_121150,RMVar_hsa_circ_378566,RMVar_hsa_circ_249123,RMVar_hsa_circ_378886,RMVar_hsa_circ_273343,RMVar_hsa_circ_329931,RMVar_hsa_circ_368197,RMVar_hsa_circ_377990,RMVar_hsa_circ_369520,RMVar_hsa_circ_319412,RMVar_hsa_circ_99502,RMVar_hsa_circ_87632,RMVar_hsa_circ_249128,RMVar_hsa_circ_249130,RMVar_hsa_circ_249131,RMVar_hsa_circ_249129,RMVar_hsa_circ_339562,RMVar_hsa_circ_249127,RMVar_hsa_circ_362962,RMVar_hsa_circ_333834,RMVar_hsa_circ_292905,RMVar_hsa_circ_308277,RMVar_hsa_circ_288966,RMVar_hsa_circ_96347,RMVar_hsa_circ_249132,RMVar_hsa_circ_249134,RMVar_hsa_circ_249136,RMVar_hsa_circ_249137,RMVar_hsa_circ_249135,RMVar_hsa_circ_249133,RMVar_hsa_circ_249138,RMVar_hsa_circ_374277,RMVar_hsa_circ_377646,RMVar_hsa_circ_267100,RMVar_hsa_circ_118872,RMVar_hsa_circ_377472,RMVar_hsa_circ_249140,RMVar_hsa_circ_249141,RMVar_hsa_circ_249139 16372 RMVar_ID_16372 Human_SNP_ID_342624848 A-to-I Human chr7 - 140774645 140774645 140774645 AGGTGTGGTGGCACTTGCCTGTAGTCCTAGCTACTCACTAGGCTGAGTTGGGAGGATCACTTGAG AGGTGTGGTGGCACTTGCCTGTAGTCCTAGCTGCTCACTAGGCTGAGTTGGGAGGATCACTTGAG T C BRAF Ensembl:ENSG00000157764 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs746403882 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16046116 RMVar_hsa_circ_79167,RMVar_hsa_circ_42798,RMVar_hsa_circ_249126,RMVar_hsa_circ_249124,RMVar_hsa_circ_121150,RMVar_hsa_circ_378566,RMVar_hsa_circ_249123,RMVar_hsa_circ_378886,RMVar_hsa_circ_273343,RMVar_hsa_circ_329931,RMVar_hsa_circ_368197,RMVar_hsa_circ_377990,RMVar_hsa_circ_369520,RMVar_hsa_circ_319412,RMVar_hsa_circ_99502,RMVar_hsa_circ_87632,RMVar_hsa_circ_249128,RMVar_hsa_circ_249130,RMVar_hsa_circ_249131,RMVar_hsa_circ_249129,RMVar_hsa_circ_339562,RMVar_hsa_circ_249127,RMVar_hsa_circ_362962,RMVar_hsa_circ_333834,RMVar_hsa_circ_292905,RMVar_hsa_circ_308277,RMVar_hsa_circ_288966,RMVar_hsa_circ_96347,RMVar_hsa_circ_249132,RMVar_hsa_circ_249134,RMVar_hsa_circ_249136,RMVar_hsa_circ_249137,RMVar_hsa_circ_249135,RMVar_hsa_circ_249133,RMVar_hsa_circ_249138,RMVar_hsa_circ_374277,RMVar_hsa_circ_377646,RMVar_hsa_circ_267100,RMVar_hsa_circ_118872,RMVar_hsa_circ_377472,RMVar_hsa_circ_249140,RMVar_hsa_circ_249141,RMVar_hsa_circ_249139 16373 RMVar_ID_16373 Human_SNP_ID_342628223 A-to-I Human chr7 - 140788674 140788674 140788674 TGAGGCAGGAGGATCACTTGAACCCAAGAGGCAGAGGTTGCAATAAGCCAAGATCACGCCACTGC TGAGGCAGGAGGATCACTTGAACCCAAGAGGCGGAGGTTGCAATAAGCCAAGATCACGCCACTGC T C BRAF Ensembl:ENSG00000157764 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1015735877 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18242,RMVar_hsa_circ_79167,RMVar_hsa_circ_249126,RMVar_hsa_circ_249124,RMVar_hsa_circ_121150,RMVar_hsa_circ_378566,RMVar_hsa_circ_249123,RMVar_hsa_circ_378886,RMVar_hsa_circ_273343,RMVar_hsa_circ_329931,RMVar_hsa_circ_377990,RMVar_hsa_circ_369520,RMVar_hsa_circ_249128,RMVar_hsa_circ_339562,RMVar_hsa_circ_249127,RMVar_hsa_circ_308277,RMVar_hsa_circ_288966,RMVar_hsa_circ_48469,RMVar_hsa_circ_249136,RMVar_hsa_circ_249137,RMVar_hsa_circ_249135,RMVar_hsa_circ_249138,RMVar_hsa_circ_374277,RMVar_hsa_circ_267100,RMVar_hsa_circ_377472,RMVar_hsa_circ_249141,RMVar_hsa_circ_349388,RMVar_hsa_circ_333089,RMVar_hsa_circ_285708,RMVar_hsa_circ_295719,RMVar_hsa_circ_270290,RMVar_hsa_circ_90659,RMVar_hsa_circ_249142,RMVar_hsa_circ_249146,RMVar_hsa_circ_249148,RMVar_hsa_circ_249147,RMVar_hsa_circ_249144,RMVar_hsa_circ_249145,RMVar_hsa_circ_249143,RMVar_hsa_circ_111177,RMVar_hsa_circ_249154,RMVar_hsa_circ_266102,RMVar_hsa_circ_373271,RMVar_hsa_circ_325059,RMVar_hsa_circ_313121,RMVar_hsa_circ_31774,RMVar_hsa_circ_58255,RMVar_hsa_circ_249156,RMVar_hsa_circ_249158,RMVar_hsa_circ_108773,RMVar_hsa_circ_365160,RMVar_hsa_circ_23485,RMVar_hsa_circ_49932 16374 RMVar_ID_16374 Human_SNP_ID_342648005 A-to-I Human chr7 - 140872012 140872012 140872012 GGGGTTCACCATGTTGGTCAGGCTAGTCTCGAACTCCTGACTTCAAGTGATCCACCTGCCGCGGC GGGGTTCACCATGTTGGTCAGGCTAGTCTCGATCTCCTGACTTCAAGTGATCCACCTGCCGCGGC T A BRAF Ensembl:ENSG00000157764 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1197810108 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90659,RMVar_hsa_circ_249142,RMVar_hsa_circ_126288,RMVar_hsa_circ_249169,RMVar_hsa_circ_249171,RMVar_hsa_circ_122968 16375 RMVar_ID_16375 Human_SNP_ID_342658014 A-to-I Human chr7 - 140912109 140912109 140912109 TCACTCTGCTACCCAGGCTGGGGTGCAGTGGCACAGTCATAGCTCACTGCAGCCTCCAACTCCTG TCACTCTGCTACCCAGGCTGGGGTGCAGTGGCGCAGTCATAGCTCACTGCAGCCTCCAACTCCTG T C BRAF Ensembl:ENSG00000157764 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1172031993 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90659,RMVar_hsa_circ_249142,RMVar_hsa_circ_126288,RMVar_hsa_circ_249169,RMVar_hsa_circ_249171,RMVar_hsa_circ_122968 16376 RMVar_ID_16376 Human_SNP_ID_342821811 A-to-I Human chr7 + 141624280 141624280 141624280 ATTGTGGACCAAAGGTCATCAATAGATGAACTACTGTCTTGGCAACAAAGTGAGACCCCATCTAT ATTGTGGACCAAAGGTCATCAATAGATGAACTGCTGTCTTGGCAACAAAGTGAGACCCCATCTAT A G AGK Ensembl:ENSG00000006530 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1252975059 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_930641 RMVar_hsa_circ_29054,RMVar_hsa_circ_76012,RMVar_hsa_circ_110061,RMVar_hsa_circ_249185,RMVar_hsa_circ_114704,RMVar_hsa_circ_249188,RMVar_hsa_circ_249189,RMVar_hsa_circ_343885,RMVar_hsa_circ_358597,RMVar_hsa_circ_350765,RMVar_hsa_circ_346351,RMVar_hsa_circ_351545,RMVar_hsa_circ_278087,RMVar_hsa_circ_249193,RMVar_hsa_circ_249194,RMVar_hsa_circ_328116 16377 RMVar_ID_16377 Human_SNP_ID_342821812 A-to-I Human chr7 + 141624294 141624294 141624294 GTCATCAATAGATGAACTACTGTCTTGGCAACAAAGTGAGACCCCATCTATACAAAAAAACTTTG GTCATCAATAGATGAACTACTGTCTTGGCAACGAAGTGAGACCCCATCTATACAAAAAAACTTTG A G AGK Ensembl:ENSG00000006530 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1222239227 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_930641 RMVar_hsa_circ_29054,RMVar_hsa_circ_76012,RMVar_hsa_circ_110061,RMVar_hsa_circ_249185,RMVar_hsa_circ_114704,RMVar_hsa_circ_249188,RMVar_hsa_circ_249189,RMVar_hsa_circ_343885,RMVar_hsa_circ_358597,RMVar_hsa_circ_350765,RMVar_hsa_circ_346351,RMVar_hsa_circ_351545,RMVar_hsa_circ_278087,RMVar_hsa_circ_249193,RMVar_hsa_circ_249194,RMVar_hsa_circ_328116 16378 RMVar_ID_16378 Human_SNP_ID_342822043 A-to-I Human chr7 + 141625489 141625489 141625489 TTCCTGCTTCCACCTCCTAAGTAGCTGGGACTATAGGCCCATACCACCATGCCTAATTTTTTACA TTCCTGCTTCCACCTCCTAAGTAGCTGGGACTGTAGGCCCATACCACCATGCCTAATTTTTTACA A G AGK Ensembl:ENSG00000006530 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1462363163 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29054,RMVar_hsa_circ_76012,RMVar_hsa_circ_110061,RMVar_hsa_circ_249185,RMVar_hsa_circ_114704,RMVar_hsa_circ_249188,RMVar_hsa_circ_249189,RMVar_hsa_circ_343885,RMVar_hsa_circ_358597,RMVar_hsa_circ_350765,RMVar_hsa_circ_346351,RMVar_hsa_circ_351545,RMVar_hsa_circ_278087,RMVar_hsa_circ_249193,RMVar_hsa_circ_249194,RMVar_hsa_circ_328116 16379 RMVar_ID_16379 Human_SNP_ID_342835201 A-to-I Human chr7 - 141684196 141684196 141684196 ATGGTGGCTCACGCCTGTAATCCCAGCACTTTAGGAGGCCAAGGAGGATCAATTTAGGAGGATCA ATGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGAGGATCAATTTAGGAGGATCA T C DENND11 Ensembl:ENSG00000257093 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934917610 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_249206,RMVar_hsa_circ_91420,RMVar_hsa_circ_249207 16380 RMVar_ID_16380 Human_SNP_ID_342851013 A-to-I Human chr7 + 141747507 141747507 141747507 CGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCACGCG CGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCGGCCTCCTGAGTAGCTGGGACTACAGGCACGCG A G SSBP1 Ensembl:ENSG00000106028 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1355741526 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64667,RMVar_hsa_circ_95680,RMVar_hsa_circ_249211,RMVar_hsa_circ_249213,RMVar_hsa_circ_91377 16381 RMVar_ID_16381 Human_SNP_ID_342863347 A-to-I Human chr7 + 141794052 141794052 141794052 TGAAAAAATGTGGATGAACCAGGAGGACCATTATGCTAACTGAAATAAGCCACATACAGAAAGAC TGAAAAAATGTGGATGAACCAGGAGGACCATTGTGCTAACTGAAATAAGCCACATACAGAAAGAC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1012666249 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16053663 16382 RMVar_ID_16382 Human_SNP_ID_343095857 A-to-I Human chr7 - 142667090 142667087 142667091 AATGCTAGAGGTGATGTTTTTGGTAAACAGGCAGGGTAAAATTTGCCGAGTTCCTTTTAATTTTT AATGCTAGAGGTGATGTTTTTGGTAAACAGG____GTAAAATTTGCCGAGTTCCTTTTAATTTTT CCCTG C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1283801283 Functional Loss DEL dbSNP153 32..35 33 - - - 16383 RMVar_ID_16383 Human_SNP_ID_343135712 A-to-I Human chr7 - 142802171 142802171 142802171 TCAGCACGAGGGCACTGACCAGCACGGCATACAAGGTGGCCTTCCCTAGCAAGATCTCATAGAGG TCAGCACGAGGGCACTGACCAGCACGGCATACGAGGTGGCCTTCCCTAGCAAGATCTCATAGAGG T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1554512982 Functional Loss SNV dbSNP153 33..33 33 - - - 16384 RMVar_ID_16384 Human_SNP_ID_343256053 A-to-I Human chr7 + 143293197 143293197 143293197 TCACCCAGGCTGGAATGCAGTGACACCACCATAGCTCACTGCAGCGTTGAACTCCTGGGTTGAAG TCACCCAGGCTGGAATGCAGTGACACCACCATGGCTCACTGCAGCGTTGAACTCCTGGGTTGAAG A G CASP2 Ensembl:ENSG00000106144 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs568638147 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_932864 RMVar_hsa_circ_83349,RMVar_hsa_circ_13826,RMVar_hsa_circ_26969,RMVar_hsa_circ_249240,RMVar_hsa_circ_80492,RMVar_hsa_circ_249241,RMVar_hsa_circ_319208,RMVar_hsa_circ_249242 16385 RMVar_ID_16385 Human_SNP_ID_343260955 A-to-I Human chr7 - 143312857 143312857 143312857 AACATATATCCCAGATTTCTGCAGCAGAAGATAATGACGAAAGTCTTCTTGGACACTTAATGATT AACATATATCCCAGATTTCTGCAGCAGAAGATGATGACGAAAGTCTTCTTGGACACTTAATGATT T C HINT1P1 Ensembl:ENSG00000231531 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs944266837 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26544726 16386 RMVar_ID_16386 Human_SNP_ID_343260956 A-to-I Human chr7 - 143312867 143312867 143312867 ATATCGAAAAAACATATATCCCAGATTTCTGCAGCAGAAGATAATGACGAAAGTCTTCTTGGACA ATATCGAAAAAACATATATCCCAGATTTCTGCGGCAGAAGATAATGACGAAAGTCTTCTTGGACA T C HINT1P1 Ensembl:ENSG00000231531 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879191110 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26544726 16387 RMVar_ID_16387 Human_SNP_ID_343327294 A-to-I Human chr7 + 143706250 143706250 143706250 GCTTTATTTCTATCATTAGTACATTTTAATATATAATGAAATAATTATACAACCCACCATAATGT GCTTTATTTCTATCATTAGTACATTTTAATATGTAATGAAATAATTATACAACCCACCATAATGT A G TCAF2 Ensembl:ENSG00000170379 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1382080948 Functional Loss SNV dbSNP153 33..33 33 - - - 16388 RMVar_ID_16388 Human_SNP_ID_343914564 A-to-I Human chr7 + 146151240 146151240 146151240 ATTTGGGTGGGGACACTAAGCCTAACCATATCATTCTCTTAGCAGTTTTCAACTATGCAATACAT ATTTGGGTGGGGACACTAAGCCTAACCATATCTTTCTCTTAGCAGTTTTCAACTATGCAATACAT A T CNTNAP2 Ensembl:ENSG00000174469 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs913086430 Functional Loss SNV dbSNP153 33..33 33 - - - 16389 RMVar_ID_16389 Human_SNP_ID_343915058 A-to-I Human chr7 + 146152240 146152240 146152240 TTTCAATAATATACCTGAACCTGGAGGAAATTATGTTAAATGAAATAAGCCAGACATAGAAAGAC TTTCAATAATATACCTGAACCTGGAGGAAATTGTGTTAAATGAAATAAGCCAGACATAGAAAGAC A G CNTNAP2 Ensembl:ENSG00000174469 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1186288437 Functional Loss SNV dbSNP153 33..33 33 - - - 16390 RMVar_ID_16390 Human_SNP_ID_343947577 A-to-I Human chr7 + 146282099 146282099 146282099 GTTAGCATTGCTGTTTGAGTCTCCACAGATGTATGTTCATCAGTGCTTGCCTATTGACCAGTCTT GTTAGCATTGCTGTTTGAGTCTCCACAGATGTGTGTTCATCAGTGCTTGCCTATTGACCAGTCTT A G CNTNAP2 Ensembl:ENSG00000174469 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs895437545 Functional Loss SNV dbSNP153 33..33 33 - - - 16391 RMVar_ID_16391 Human_SNP_ID_343975242 A-to-I Human chr7 + 146388175 146388175 146388175 GCTTTTGGCCGGGCATGAGGTCTCACGTTGGTAATCCTCGCACTTTGAGACGCTGAGGCAGGAGG GCTTTTGGCCGGGCATGAGGTCTCACGTTGGTGATCCTCGCACTTTGAGACGCTGAGGCAGGAGG A G CNTNAP2 Ensembl:ENSG00000174469 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1334469317 Functional Loss SNV dbSNP153 33..33 33 - - - 16392 RMVar_ID_16392 Human_SNP_ID_344001532 A-to-I Human chr7 + 146488758 146488758 146488758 TCAGGTGATCTTCCCACCTCACCTGCCCAAGTAGCTGGGATTTCAGGCACGTGCCACCACGCCTG TCAGGTGATCTTCCCACCTCACCTGCCCAAGTTGCTGGGATTTCAGGCACGTGCCACCACGCCTG A T CNTNAP2 Ensembl:ENSG00000174469 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1445304956 Functional Loss SNV dbSNP153 33..33 33 - - - 16393 RMVar_ID_16393 Human_SNP_ID_344027028 A-to-I Human chr7 + 146585177 146585177 146585177 CGGAGTCCCACTCTATCGCCAGACTGGAGTGCAGTGGCACGATCTCGGCTCACTGCAACCTCTGA CGGAGTCCCACTCTATCGCCAGACTGGAGTGCGGTGGCACGATCTCGGCTCACTGCAACCTCTGA A G CNTNAP2 Ensembl:ENSG00000174469 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1323604082 Functional Loss SNV dbSNP153 33..33 33 - - - 16394 RMVar_ID_16394 Human_SNP_ID_344027402 A-to-I Human chr7 + 146586374 146586374 146586374 ATACTTAGCCTCATCCTTAATCAAAGTGTAATAAATTACAAACCCCACCAAAATCTCTACCTACT ATACTTAGCCTCATCCTTAATCAAAGTGTAATGAATTACAAACCCCACCAAAATCTCTACCTACT A G CNTNAP2 Ensembl:ENSG00000174469 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs909151660 Functional Loss SNV dbSNP153 33..33 33 - - - 16395 RMVar_ID_16395 Human_SNP_ID_344027465 A-to-I Human chr7 + 146586611 146586611 146586611 CACCAAAGGTAATTAACCATCAGATGTATATTAATCACACACACATAAACATGCACACATATGTA CACCAAAGGTAATTAACCATCAGATGTATATTCATCACACACACATAAACATGCACACATATGTA A C CNTNAP2 Ensembl:ENSG00000174469 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs757087316 Functional Loss SNV dbSNP153 33..33 33 - - - 16396 RMVar_ID_16396 Human_SNP_ID_344048223 A-to-I Human chr7 + 146662397 146662397 146662397 GACCTCAGTTGATCCGCCCACCTCGGCCTCCCAAAGTGTTCAGATTGCAGGCGTCAGCCACTGCA GACCTCAGTTGATCCGCCCACCTCGGCCTCCCCAAGTGTTCAGATTGCAGGCGTCAGCCACTGCA A C CNTNAP2 Ensembl:ENSG00000174469 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1042938949 Functional Loss SNV dbSNP153 33..33 33 - - - 16397 RMVar_ID_16397 Human_SNP_ID_344607731 A-to-I Human chr7 + 148795107 148795107 148795107 TGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTATAGGCGTGAGCCACCGTGCCTGGCAGAGTTGT TGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTGTAGGCGTGAGCCACCGTGCCTGGCAGAGTTGT A G CUL1 Ensembl:ENSG00000055130 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1473377718 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114310,RMVar_hsa_circ_249285,RMVar_hsa_circ_366619,RMVar_hsa_circ_43770,RMVar_hsa_circ_16355,RMVar_hsa_circ_117283,RMVar_hsa_circ_249300 16398 RMVar_ID_16398 Human_SNP_ID_344628950 A-to-I Human chr7 - 148870491 148870491 148870491 CGCCATGTTGCCCCGGCTGGTCTAGAACTCCTAGGATCAAGTGATCTCCCACCTTGGAGTCCCCA CGCCATGTTGCCCCGGCTGGTCTAGAACTCCTGGGATCAAGTGATCTCCCACCTTGGAGTCCCCA T C EZH2 Ensembl:ENSG00000106462 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1455586487 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16060649 RMVar_hsa_circ_79673,RMVar_hsa_circ_249327 16399 RMVar_ID_16399 Human_SNP_ID_344629326 A-to-I Human chr7 - 148871713 148871713 148871713 AAAGTTAGCTAGGTGTGGTGGCATGCGCCTGTAGTTTCAGCTACTTAGGAGGCTGAGACAGGAGG AAAGTTAGCTAGGTGTGGTGGCATGCGCCTGTGGTTTCAGCTACTTAGGAGGCTGAGACAGGAGG T C EZH2 Ensembl:ENSG00000106462 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1405498574 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79673,RMVar_hsa_circ_249327 16400 RMVar_ID_16400 Human_SNP_ID_344666400 A-to-I Human chr7 - 149009069 149009069 149009069 TAACATAGCCAGGCATGATGGCATATGCCTATAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAAG TAACATAGCCAGGCATGATGGCATATGCCTATGGTCCCAGCTACTTGGGAGGCTGAGGCAGGAAG T C PDIA4 Ensembl:ENSG00000155660 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1302235218 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_541,RMVar_hsa_circ_371845,RMVar_hsa_circ_249333 16401 RMVar_ID_16401 Human_SNP_ID_344666430 A-to-I Human chr7 - 149009225 149009225 149009225 CCAGGCTGGTCTTAAACTCTTGGGGTTGGCTGAGCACAGTGGCTCATGCCTGTAATCCCAGCACT CCAGGCTGGTCTTAAACTCTTGGGGTTGGCTGGGCACAGTGGCTCATGCCTGTAATCCCAGCACT T C PDIA4 Ensembl:ENSG00000155660 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1454056779 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_541,RMVar_hsa_circ_371845,RMVar_hsa_circ_249333 16402 RMVar_ID_16402 Human_SNP_ID_344668749 A-to-I Human chr7 - 149017515 149017515 149017515 CGATGGCGCAATCTCAGCTCACCGCAACCTCCACCTCCCGGATTCAAGTGATTCTCCTGCCTCAG CGATGGCGCAATCTCAGCTCACCGCAACCTCCGCCTCCCGGATTCAAGTGATTCTCCTGCCTCAG T C PDIA4 Ensembl:ENSG00000155660 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1962977 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_541,RMVar_hsa_circ_371845,RMVar_hsa_circ_102100,RMVar_hsa_circ_360788,RMVar_hsa_circ_249333,RMVar_hsa_circ_249335,RMVar_hsa_circ_356601,RMVar_hsa_circ_358987 16403 RMVar_ID_16403 Human_SNP_ID_344668750 A-to-I Human chr7 - 149017515 149017515 149017515 CGATGGCGCAATCTCAGCTCACCGCAACCTCCACCTCCCGGATTCAAGTGATTCTCCTGCCTCAG CGATGGCGCAATCTCAGCTCACCGCAACCTCCCCCTCCCGGATTCAAGTGATTCTCCTGCCTCAG T G PDIA4 Ensembl:ENSG00000155660 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1962977 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_541,RMVar_hsa_circ_371845,RMVar_hsa_circ_102100,RMVar_hsa_circ_360788,RMVar_hsa_circ_249333,RMVar_hsa_circ_249335,RMVar_hsa_circ_356601,RMVar_hsa_circ_358987 16404 RMVar_ID_16404 Human_SNP_ID_344669091 A-to-I Human chr7 - 149018614 149018614 149018614 CAGCCTGACCAACATGGTGAAACCCCATCTCTACTAAAAATACAACAATTAGCTGGGTGTAGTGG CAGCCTGACCAACATGGTGAAACCCCATCTCTGCTAAAAATACAACAATTAGCTGGGTGTAGTGG T C PDIA4 Ensembl:ENSG00000155660 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1374649599 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_541,RMVar_hsa_circ_371845,RMVar_hsa_circ_102100,RMVar_hsa_circ_360788,RMVar_hsa_circ_249333,RMVar_hsa_circ_249335,RMVar_hsa_circ_356601,RMVar_hsa_circ_358987 16405 RMVar_ID_16405 Human_SNP_ID_344683827 A-to-I Human chr7 - 149069231 149069231 149069231 TTTATAGAATATAGCCTGGCGTGGTGGCTCATACCTATAATCCCATTACTTTGGGAGGTCAAGGC TTTATAGAATATAGCCTGGCGTGGTGGCTCATTCCTATAATCCCATTACTTTGGGAGGTCAAGGC T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350342819 Functional Loss SNV dbSNP153 33..33 33 - - - 16406 RMVar_ID_16406 Human_SNP_ID_344684027 A-to-I Human chr7 - 149069780 149069780 149069780 GTCTCTACTAAAAATACAAAAATTAGCCAGGCATGGTGGTACACACCAGTAGTCCCAGCTACTCC GTCTCTACTAAAAATACAAAAATTAGCCAGGCGTGGTGGTACACACCAGTAGTCCCAGCTACTCC T C ZNF786 Ensembl:ENSG00000197362 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs555899350 Functional Loss SNV dbSNP153 33..33 33 - - - 16407 RMVar_ID_16407 Human_SNP_ID_344684054 A-to-I Human chr7 - 149069910 149069910 149069910 AATTGTTATAAAAGTAAATTTAGGCCAGGCACAGTGGTTCATGCCTGTAATCCCAGCACTTGGGA AATTGTTATAAAAGTAAATTTAGGCCAGGCACGGTGGTTCATGCCTGTAATCCCAGCACTTGGGA T C ZNF786 Ensembl:ENSG00000197362 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1316892572 Functional Loss SNV dbSNP153 33..33 33 - - - 16408 RMVar_ID_16408 Human_SNP_ID_344701893 A-to-I Human chr7 + 149131539 149131539 149131539 GAAACCCCATCTCTACTACAAATACAGAAATTAGCTGGGTGTGGTGGCGGACGCCTGTAGTCCCA GAAACCCCATCTCTACTACAAATACAGAAATTGGCTGGGTGTGGTGGCGGACGCCTGTAGTCCCA A G ZNF398 Ensembl:ENSG00000197024 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs990110555 Functional Loss SNV dbSNP153 33..33 33 - - - 16409 RMVar_ID_16409 Human_SNP_ID_344701903 A-to-I Human chr7 + 149131575 149131575 149131575 GGGTGTGGTGGCGGACGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCTTAAA GGGTGTGGTGGCGGACGCCTGTAGTCCCAGCTTCTCGGGAGGCTGAGGCAGGAGAATTGCTTAAA A T ZNF398 Ensembl:ENSG00000197024 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167495171 Functional Loss SNV dbSNP153 33..33 33 - - - 16410 RMVar_ID_16410 Human_SNP_ID_344702330 A-to-I Human chr7 + 149133394 149133394 149133394 CCCCAGCCTCCCAAAGTGCTGGGATTATAGGCATGAGCCACTGTGCCAGGCCATCAGCATGGTCT CCCCAGCCTCCCAAAGTGCTGGGATTATAGGCCTGAGCCACTGTGCCAGGCCATCAGCATGGTCT A C ZNF398 Ensembl:ENSG00000197024 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs772321043 Functional Loss SNV dbSNP153 33..33 33 - - - 16411 RMVar_ID_16411 Human_SNP_ID_344702914 A-to-I Human chr7 + 149134834 149134834 149134834 CTCACCGCAACCTCTGCCTCCCTGGTTCAAGCAATTCTCATGCCTCAGCCTCCCAAGCAGCTGGG CTCACCGCAACCTCTGCCTCCCTGGTTCAAGCGATTCTCATGCCTCAGCCTCCCAAGCAGCTGGG A G ZNF398 Ensembl:ENSG00000197024 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1470231163 Functional Loss SNV dbSNP153 33..33 33 - - - 16412 RMVar_ID_16412 Human_SNP_ID_344703156 A-to-I Human chr7 + 149135685 149135685 149135685 TATTAGAATAATAATAATAGTCCGGGTGCGGTAGCTCACACCTGTAATCCCAGCACTTTGGGAGG TATTAGAATAATAATAATAGTCCGGGTGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGG A G ZNF398 Ensembl:ENSG00000197024 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs975420280 Functional Loss SNV dbSNP153 33..33 33 - - - 16413 RMVar_ID_16413 Human_SNP_ID_344703186 A-to-I Human chr7 + 149135846 149135846 149135846 GGGCATGGTGGTGCGCGCCTGTAGTCCCAGCTACTCAAGAGGCTGAGCATGAGAATCACTTGACC GGGCATGGTGGTGCGCGCCTGTAGTCCCAGCTGCTCAAGAGGCTGAGCATGAGAATCACTTGACC A G ZNF398 Ensembl:ENSG00000197024 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1483306181 Functional Loss SNV dbSNP153 33..33 33 - - - 16414 RMVar_ID_16414 Human_SNP_ID_344703187 A-to-I Human chr7 + 149135850 149135849 149135851 ATGGTGGTGCGCGCCTGTAGTCCCAGCTACTCAAGAGGCTGAGCATGAGAATCACTTGACCCCAG ATGGTGGTGCGCGCCTGTAGTCCCAGCTACTC__GAGGCTGAGCATGAGAATCACTTGACCCCAG CAA C ZNF398 Ensembl:ENSG00000197024 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1257224918 Functional Loss DEL dbSNP153 33..34 33 - - - 16415 RMVar_ID_16415 Human_SNP_ID_344703188 A-to-I Human chr7 + 149135850 149135850 149135850 ATGGTGGTGCGCGCCTGTAGTCCCAGCTACTCAAGAGGCTGAGCATGAGAATCACTTGACCCCAG ATGGTGGTGCGCGCCTGTAGTCCCAGCTACTCGAGAGGCTGAGCATGAGAATCACTTGACCCCAG A G ZNF398 Ensembl:ENSG00000197024 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928218431 Functional Loss SNV dbSNP153 33..33 33 - - - 16416 RMVar_ID_16416 Human_SNP_ID_344703195 A-to-I Human chr7 + 149135881 149135881 149135881 CAAGAGGCTGAGCATGAGAATCACTTGACCCCAGGAGGCGGACGTTGCAGTGAGCCAAGATCATG CAAGAGGCTGAGCATGAGAATCACTTGACCCCCGGAGGCGGACGTTGCAGTGAGCCAAGATCATG A C ZNF398 Ensembl:ENSG00000197024 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1024804150 Functional Loss SNV dbSNP153 33..33 33 - - - 16417 RMVar_ID_16417 Human_SNP_ID_344706881 A-to-I Human chr7 + 149150543 149150543 149150543 ATCGCTTGAGCCCATGAGATGGAGGTTGCGGTAAGCTGAGATTACACCACTGCACTCCAGCCTGG ATCGCTTGAGCCCATGAGATGGAGGTTGCGGTGAGCTGAGATTACACCACTGCACTCCAGCCTGG A G ZNF398 Ensembl:ENSG00000197024 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1452953302 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26082704 16418 RMVar_ID_16418 Human_SNP_ID_344713481 A-to-I Human chr7 + 149174775 149174775 149174775 TTGAGCCTGGGAGGCAGAGATTGCAGTAAGCCAAGATTACGCCACTGTAGTCCAGCCTGGGTGAT TTGAGCCTGGGAGGCAGAGATTGCAGTAAGCCGAGATTACGCCACTGTAGTCCAGCCTGGGTGAT A G ZNF398 Ensembl:ENSG00000197024 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs996572068 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_304748 16419 RMVar_ID_16419 Human_SNP_ID_344715880 A-to-I Human chr7 + 149183711 149183711 149183711 GTTGCTTAGGCTGGTCTTGAACTCCTAAGTTCAAGTGATCCTCCTGCCAAGGCCTCCCAAAGAGC GTTGCTTAGGCTGGTCTTGAACTCCTAAGTTCGAGTGATCCTCCTGCCAAGGCCTCCCAAAGAGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1296970527 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16062612 16420 RMVar_ID_16420 Human_SNP_ID_344716540 A-to-I Human chr7 + 149186371 149186371 149186371 TTGGCTCGTTGCAACCTCTGGCTCCCAGCTTCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGC TTGGCTCGTTGCAACCTCTGGCTCCCAGCTTCGAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1352638683 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16062687 16421 RMVar_ID_16421 Human_SNP_ID_344720965 A-to-I Human chr7 + 149203492 149203492 149203492 CCTCAGTCTCTCAATTAATTAGGACTATAGGCACATGCCACCACACCCAGTTAAGTTTTTTATTT CCTCAGTCTCTCAATTAATTAGGACTATAGGCTCATGCCACCACACCCAGTTAAGTTTTTTATTT A T ZNF282 Ensembl:ENSG00000170265 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs536525000 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16063075 RMVar_hsa_circ_2445,RMVar_hsa_circ_119296,RMVar_hsa_circ_73751,RMVar_hsa_circ_249347 16422 RMVar_ID_16422 Human_SNP_ID_344722201 A-to-I Human chr7 + 149208259 149208259 149208259 TGGTTCAGGCTGGAATGCAGCGGTGCAATCTCAGCTCACTGCAACCTCCGTCTCCCAGATTCAAG TGGTTCAGGCTGGAATGCAGCGGTGCAATCTCGGCTCACTGCAACCTCCGTCTCCCAGATTCAAG A G ZNF282 Ensembl:ENSG00000170265 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1563177422 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17577990 RMVar_hsa_circ_2445,RMVar_hsa_circ_119296,RMVar_hsa_circ_249347,RMVar_hsa_circ_302404,RMVar_hsa_circ_249349,RMVar_hsa_circ_249350,RMVar_hsa_circ_376227 16423 RMVar_ID_16423 Human_SNP_ID_344722238 A-to-I Human chr7 + 149208437 149208437 149208437 GTTGGCCAGGCTGGTCTTGAACTCCTGACCTCAAGTGATCCACCCGCCTCGGCCTCCCAAAGTGC GTTGGCCAGGCTGGTCTTGAACTCCTGACCTCGAGTGATCCACCCGCCTCGGCCTCCCAAAGTGC A G ZNF282 Ensembl:ENSG00000170265 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs984939651 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2445,RMVar_hsa_circ_119296,RMVar_hsa_circ_249347,RMVar_hsa_circ_302404,RMVar_hsa_circ_249349,RMVar_hsa_circ_249350,RMVar_hsa_circ_376227 16424 RMVar_ID_16424 Human_SNP_ID_344727450 A-to-I Human chr7 + 149227894 149227894 149227894 CATCACCACACCTGGCTATTTTGTTTTTCTTTACTTTTTGTAGAGATAGGGTCTTGCTATGTTGC CATCACCACACCTGGCTATTTTGTTTTTCTTTGCTTTTTGTAGAGATAGGGTCTTGCTATGTTGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs533081822 Functional Loss SNV dbSNP153 33..33 33 - - - 16425 RMVar_ID_16425 Human_SNP_ID_344732348 A-to-I Human chr7 + 149245560 149245560 149245560 TTGAGACAGAATCTCTCTCTGTCACTGGAGGGAAGTGGTGTGATCATGGCTTCCTGCAGCCTCAA TTGAGACAGAATCTCTCTCTGTCACTGGAGGGCAGTGGTGTGATCATGGCTTCCTGCAGCCTCAA A C ZNF212 Ensembl:ENSG00000170260 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs944459885 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_177595 16426 RMVar_ID_16426 Human_SNP_ID_344733988 A-to-I Human chr7 + 149251836 149251836 149251836 TAATATTTAAGACTATTTGAGATGGGTGTGGTAGCTCACATCTGTAATCCCAACACTTTGGGAGG TAATATTTAAGACTATTTGAGATGGGTGTGGTTGCTCACATCTGTAATCCCAACACTTTGGGAGG A T ZNF212 Ensembl:ENSG00000170260 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs562920388 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_345705,RMVar_hsa_circ_72526 16427 RMVar_ID_16427 Human_SNP_ID_344740823 A-to-I Human chr7 + 149276152 149276152 149276152 AGCTCAAGCAGTTCTCCCATCTTGGCCTCCCAAAGTGTTGGGATTACAGGCATGAGCCACTACGC AGCTCAAGCAGTTCTCCCATCTTGGCCTCCCAGAGTGTTGGGATTACAGGCATGAGCCACTACGC A G ZNF783 Ensembl:ENSG00000204946 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs4727037 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_1153,GWAS_ID_1154,GWAS_ID_1155,GWAS_ID_1156 RMVar_hsa_circ_347241,RMVar_hsa_circ_317080,RMVar_hsa_circ_96115,RMVar_hsa_circ_249358,RMVar_hsa_circ_249355,RMVar_hsa_circ_249354,RMVar_hsa_circ_103633 16428 RMVar_ID_16428 Human_SNP_ID_557242818 A-to-I Human chr14 + 60100392 60100392 60100392 GCCATCTTGGCTCACTACAACCTCTGTCTCCCAGGTTCAAGTGATTCTCCCGCCTCAGCCTCCCA GCCATCTTGGCTCACTACAACCTCTGTCTCCCGGGTTCAAGTGATTCTCCCGCCTCAGCCTCCCA A G PCNX4 Ensembl:ENSG00000126773 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs894635450 Functional Loss SNV dbSNP153 33..33 33 - - - 16429 RMVar_ID_16429 Human_SNP_ID_557242840 A-to-I Human chr14 + 60100546 60100546 60100546 GTCTTGAACTCCCGACCTCAGGTGATCTGCCCACCTCAGCCTCTCAAAGTGCTGGGATTACAGGC GTCTTGAACTCCCGACCTCAGGTGATCTGCCCGCCTCAGCCTCTCAAAGTGCTGGGATTACAGGC A G PCNX4 Ensembl:ENSG00000126773 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1485253466 Functional Loss SNV dbSNP153 33..33 33 - - - 16430 RMVar_ID_16430 Human_SNP_ID_557246153 A-to-I Human chr14 + 60113071 60113071 60113071 GGGCGTGGTGGCGTGTGCCTGTAGTCCCAGCTACTGGGGGGCTGAGGCAGGAGAATCGCTTGAAC GGGCGTGGTGGCGTGTGCCTGTAGTCCCAGCTGCTGGGGGGCTGAGGCAGGAGAATCGCTTGAAC A G PCNX4 Ensembl:ENSG00000126773 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs558039301 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167030,RMVar_hsa_circ_167032,RMVar_hsa_circ_332830,RMVar_hsa_circ_352722,RMVar_hsa_circ_167031 16431 RMVar_ID_16431 Human_SNP_ID_557254050 A-to-I Human chr14 + 60142753 60142753 60142753 GGGAGGCCAGGGCGGGTGGATCATTTGAGGTCAGGAGTTTGAGACCAGCCTGGCCAACATGGTGA GGGAGGCCAGGGCGGGTGGATCATTTGAGGTCCGGAGTTTGAGACCAGCCTGGCCAACATGGTGA A C PCNX4 Ensembl:ENSG00000126773 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs976790399 Functional Loss SNV dbSNP153 33..33 33 - - - 16432 RMVar_ID_16432 Human_SNP_ID_557315444 A-to-I Human chr14 + 60397860 60397859 60397861 CATTCACAAACTGAAAGAAAAAGCGAAGAAACAGAAGGGTCGCGGCTTTGGCTCCGAAGAGGGGT CATTCACAAACTGAAAGAAAAAGCGAAGAAAC__AAGGGTCGCGGCTTTGGCTCCGAAGAGGGGT CAG C RBM8B Ensembl:ENSG00000258427 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs758420993 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_5095320,Human_RBP_ID_5564058 16433 RMVar_ID_16433 Human_SNP_ID_557315446 A-to-I Human chr14 + 60397860 60397860 60397860 CATTCACAAACTGAAAGAAAAAGCGAAGAAACAGAAGGGTCGCGGCTTTGGCTCCGAAGAGGGGT CATTCACAAACTGAAAGAAAAAGCGAAGAAACGGAAGGGTCGCGGCTTTGGCTCCGAAGAGGGGT A G RBM8B Ensembl:ENSG00000258427 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs748686203 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5095320,Human_RBP_ID_5564058 16434 RMVar_ID_16434 Human_SNP_ID_557393630 A-to-I Human chr14 - 60717137 60717137 60717137 CCAGGAGGTGGAGGTTGCAGTGAGCCGAGATCACGCCATTGCACTCCAGCCTGGGCAACAAGAGC CCAGGAGGTGGAGGTTGCAGTGAGCCGAGATCGCGCCATTGCACTCCAGCCTGGGCAACAAGAGC T C SIX4 Ensembl:ENSG00000100625 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1456008380 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125678,RMVar_hsa_circ_167054 16435 RMVar_ID_16435 Human_SNP_ID_557393675 A-to-I Human chr14 - 60717331 60717331 60717331 CAGTGGCTTACGCCTGTTAATCCCAGCACTTTAGGAGGCTAAGGCGGGTGGATCACCTGAGGTCA CAGTGGCTTACGCCTGTTAATCCCAGCACTTTGGGAGGCTAAGGCGGGTGGATCACCTGAGGTCA T C SIX4 Ensembl:ENSG00000100625 Protein coding intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs558307839 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125678,RMVar_hsa_circ_167054 16436 RMVar_ID_16436 Human_SNP_ID_557393779 A-to-I Human chr14 - 60717840 60717840 60717840 GACCGGCTAATCTTCGTGTGTTTAACAGAGAGAGGGTTTTGCTATGTTGGCCAGGCTGGTCTTGA GACCGGCTAATCTTCGTGTGTTTAACAGAGAGCGGGTTTTGCTATGTTGGCCAGGCTGGTCTTGA T G SIX4 Ensembl:ENSG00000100625 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041662031 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3454771 RMVar_hsa_circ_125678,RMVar_hsa_circ_167054 16437 RMVar_ID_16437 Human_SNP_ID_557408723 A-to-I Human chr14 - 60780349 60780349 60780349 ATCTGTCTGATGACTGAACGGATTTCATCCTGAATAGCTTTCTGAGACTTTTCTCTGGGTGCACT ATCTGTCTGATGACTGAACGGATTTCATCCTGGATAGCTTTCTGAGACTTTTCTCTGGGTGCACT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs920787372 Functional Loss SNV dbSNP153 33..33 33 - - - 16438 RMVar_ID_16438 Human_SNP_ID_557411651 A-to-I Human chr14 + 60793504 60793504 60793504 CCTGCCTCAGCCTCCTGAGTAGCTAGGACTACAGGCATGCACCACCACATCTAGCTAATTTTTTT CCTGCCTCAGCCTCCTGAGTAGCTAGGACTACTGGCATGCACCACCACATCTAGCTAATTTTTTT A T MNAT1 Ensembl:ENSG00000020426 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1032688724 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167060,RMVar_hsa_circ_167058,RMVar_hsa_circ_167059,RMVar_hsa_circ_167061 16439 RMVar_ID_16439 Human_SNP_ID_557436372 A-to-I Human chr14 + 60899159 60899159 60899159 TTTTATCTTAATTTCATGTAGAGCTTGTCTTTATACTGCTTTGTGGTAGCTACAATGCTCTATCA TTTTATCTTAATTTCATGTAGAGCTTGTCTTTTTACTGCTTTGTGGTAGCTACAATGCTCTATCA A T AL160236.2,MNAT1 Ensembl:ENSG00000258892,Ensembl:ENSG00000020426 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs962437744 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1821737,Human_RBP_ID_9043566 16440 RMVar_ID_16440 Human_SNP_ID_557449257 A-to-I Human chr14 + 60947019 60947019 60947019 TGTTCTCTGGTATCTGTTCTTGTAAGGGCATTAATATAGTCATGAAGGCTCCACCCTCGTGAATT TGTTCTCTGGTATCTGTTCTTGTAAGGGCATTCATATAGTCATGAAGGCTCCACCCTCGTGAATT A C AL160236.2,MNAT1 Ensembl:ENSG00000258892,Ensembl:ENSG00000020426 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs747890632 Functional Loss SNV dbSNP153 33..33 33 - - - 16441 RMVar_ID_16441 Human_SNP_ID_557449265 A-to-I Human chr14 + 60947053 60947053 60947053 TATAGTCATGAAGGCTCCACCCTCGTGAATTCATGTAAACCTGAATGCCTCACAAAGACCCCATT TATAGTCATGAAGGCTCCACCCTCGTGAATTCGTGTAAACCTGAATGCCTCACAAAGACCCCATT A G AL160236.2,MNAT1 Ensembl:ENSG00000258892,Ensembl:ENSG00000020426 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs527518561 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12375465,Human_RBP_ID_23306856 16442 RMVar_ID_16442 Human_SNP_ID_557460044 A-to-I Human chr14 + 60993082 60993082 60993082 GTTGGCCAGGCTGGTATAGAACTCCTGACTTCAGGTGATCTGCCCACCTCGGCCTCCCAAACGGT GTTGGCCAGGCTGGTATAGAACTCCTGACTTCGGGTGATCTGCCCACCTCGGCCTCCCAAACGGT A G SLC38A6 Ensembl:ENSG00000139974 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs777917656 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44909,RMVar_hsa_circ_303383,RMVar_hsa_circ_310523,RMVar_hsa_circ_286251,RMVar_hsa_circ_167073,RMVar_hsa_circ_16949,RMVar_hsa_circ_167074 16443 RMVar_ID_16443 Human_SNP_ID_557479432 A-to-I Human chr14 + 61071517 61071517 61071517 CAGCCTGGGCAACATGGCAAATCCCTCTCTCTACAAAAAATACAAAAATTAGCCAGGTGTGGTGG CAGCCTGGGCAACATGGCAAATCCCTCTCTCTGCAAAAAATACAAAAATTAGCCAGGTGTGGTGG A G SLC38A6 Ensembl:ENSG00000139974 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs555845017 Functional Loss SNV dbSNP153 33..33 33 - - - 16444 RMVar_ID_16444 Human_SNP_ID_557480576 A-to-I Human chr14 + 61075886 61075886 61075886 CTCAACTTCCTTTTTTTTTGAAACGGAGTTTCACTTTTTTTGCCCAGACTGGAGTGCAATGCTGT CTCAACTTCCTTTTTTTTTGAAACGGAGTTTCCCTTTTTTTGCCCAGACTGGAGTGCAATGCTGT A C SLC38A6 Ensembl:ENSG00000139974 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1450351191 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23629874 16445 RMVar_ID_16445 Human_SNP_ID_557482457 A-to-I Human chr14 + 61083617 61083617 61083617 GGAAAGGCCACGCAAGGACACAGCAAGAAGGCAACTGTTTACAAGCCAAGGGAAGAGGCCTCAGG GGAAAGGCCACGCAAGGACACAGCAAGAAGGCGACTGTTTACAAGCCAAGGGAAGAGGCCTCAGG A G SLC38A6 Ensembl:ENSG00000139974 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956326223 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27808358 Human_Splice_Rec_1521996,Human_Splice_Rec_1522064,Human_Splice_Rec_1522116,Human_Splice_Rec_1522148,Human_Splice_Rec_1522212,Human_Splice_Rec_1522306 Human_miRNA_ID_593884,Human_miRNA_ID_797326,Human_miRNA_ID_801442,Human_miRNA_ID_805546,Human_miRNA_ID_809648,Human_miRNA_ID_813743,Human_miRNA_ID_2218203,Human_miRNA_ID_2335470,Human_miRNA_ID_2337703,Human_miRNA_ID_2339936,Human_miRNA_ID_2342174,Human_miRNA_ID_2344407 RMVar_hsa_circ_125652,RMVar_hsa_circ_167085 16446 RMVar_ID_16446 Human_SNP_ID_557482461 A-to-I Human chr14 + 61083627 61083627 61083627 CGCAAGGACACAGCAAGAAGGCAACTGTTTACAAGCCAAGGGAAGAGGCCTCAGGAGAACCAAAC CGCAAGGACACAGCAAGAAGGCAACTGTTTACTAGCCAAGGGAAGAGGCCTCAGGAGAACCAAAC A T SLC38A6 Ensembl:ENSG00000139974 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs142796767 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27808358 Human_Splice_Rec_1521996,Human_Splice_Rec_1522064,Human_Splice_Rec_1522116,Human_Splice_Rec_1522148,Human_Splice_Rec_1522212,Human_Splice_Rec_1522306 Human_miRNA_ID_593884,Human_miRNA_ID_797326,Human_miRNA_ID_801442,Human_miRNA_ID_805546,Human_miRNA_ID_809648,Human_miRNA_ID_813743,Human_miRNA_ID_2218203,Human_miRNA_ID_2335470,Human_miRNA_ID_2337703,Human_miRNA_ID_2339936,Human_miRNA_ID_2342174,Human_miRNA_ID_2344407 RMVar_hsa_circ_125652,RMVar_hsa_circ_167085 16447 RMVar_ID_16447 Human_SNP_ID_557571315 A-to-I Human chr14 + 61441888 61441888 61441888 GTCCAGGTGGTCTTGAACTCCTGGACTCAAGCAGTCCTCCTGCCTCAGCCTCCCAAAGTGTTGGT GTCCAGGTGGTCTTGAACTCCTGGACTCAAGCCGTCCTCCTGCCTCAGCCTCCCAAAGTGTTGGT A C PRKCH Ensembl:ENSG00000027075 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1451415379 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64761,RMVar_hsa_circ_78511,RMVar_hsa_circ_167086,RMVar_hsa_circ_353133 16448 RMVar_ID_16448 Human_SNP_ID_557601261 A-to-I Human chr14 - 61563818 61563818 61563818 CAGTACTTTCTAGGAGGCTGTAGCCTAACTGGAGAGAGAGGTGAGACCAGGGGTTCTCAGACTTG CAGTACTTTCTAGGAGGCTGTAGCCTAACTGGGGAGAGAGGTGAGACCAGGGGTTCTCAGACTTG T C LINC01303 Ensembl:ENSG00000250548 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs959683 Functional Loss SNV dbSNP153 33..33 33 - - - 16449 RMVar_ID_16449 Human_SNP_ID_557622809 A-to-I Human chr14 + 61657174 61657174 61657174 GTGGATTTTTTTTTTTGAGACAGTGTCTCACTATTGCCTATGCTGGAGTGCAGTGGCACGATCAT GTGGATTTTTTTTTTTGAGACAGTGTCTCACTCTTGCCTATGCTGGAGTGCAGTGGCACGATCAT A C AL355916.3,AL355916.1 Ensembl:ENSG00000258989,Ensembl:ENSG00000232774 Protein coding,lincRNA intron,intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1469316368 Functional Loss SNV dbSNP153 33..33 33 - - - 16450 RMVar_ID_16450 Human_SNP_ID_557643396 A-to-I Human chr14 + 61743151 61743151 61743151 CAATGGCGTGATCTCGGATCTTGGCTCACCGCAACTGCCGCCTCGCTGGTTCAAGCAAATCTCGT CAATGGCGTGATCTCGGATCTTGGCTCACCGCGACTGCCGCCTCGCTGGTTCAAGCAAATCTCGT A G HIF1A,AL137129.1 Ensembl:ENSG00000100644,Ensembl:ENSG00000258964 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1198969519 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167096,RMVar_hsa_circ_113772,RMVar_hsa_circ_167095,RMVar_hsa_circ_167106,RMVar_hsa_circ_321072,RMVar_hsa_circ_7594,RMVar_hsa_circ_13717,RMVar_hsa_circ_167107,RMVar_hsa_circ_331567,RMVar_hsa_circ_43837,RMVar_hsa_circ_108880,RMVar_hsa_circ_56077,RMVar_hsa_circ_167120,RMVar_hsa_circ_167124,RMVar_hsa_circ_280104,RMVar_hsa_circ_306207,RMVar_hsa_circ_277948,RMVar_hsa_circ_167125 16451 RMVar_ID_16451 Human_SNP_ID_557644318 A-to-I Human chr14 + 61746467 61746467 61746467 TGCCCAGGCCTGGAGTGCAGTGGCATGATCATAGCTCACTGCAGTCTCAAACTCCTGTGCTCAAG TGCCCAGGCCTGGAGTGCAGTGGCATGATCATTGCTCACTGCAGTCTCAAACTCCTGTGCTCAAG A T HIF1A,AL137129.1 Ensembl:ENSG00000100644,Ensembl:ENSG00000258964 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs574991705 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167095,RMVar_hsa_circ_167106,RMVar_hsa_circ_108880,RMVar_hsa_circ_167120 16452 RMVar_ID_16452 Human_SNP_ID_557644822 A-to-I Human chr14 - 61748740 61748740 61748740 AAACAAACCAAATTTGTTCTAAGTTTGACTTTAGAGTCAGGAAACTTAAGCTTACATTTTTGGTC AAACAAACCAAATTTGTTCTAAGTTTGACTTTGGAGTCAGGAAACTTAAGCTTACATTTTTGGTC T C HIF1A-AS3 Ensembl:ENSG00000258667 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1001681022 Functional Loss SNV dbSNP153 33..33 33 - - - 16453 RMVar_ID_16453 Human_SNP_ID_557644825 A-to-I Human chr14 - 61748751 61748751 61748751 CATTAAAACAAAAACAAACCAAATTTGTTCTAAGTTTGACTTTAGAGTCAGGAAACTTAAGCTTA CATTAAAACAAAAACAAACCAAATTTGTTCTAGGTTTGACTTTAGAGTCAGGAAACTTAAGCTTA T C HIF1A-AS3 Ensembl:ENSG00000258667 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs765445538 Functional Loss SNV dbSNP153 33..33 33 - - - 16454 RMVar_ID_16454 Human_SNP_ID_557653690 A-to-I Human chr14 + 61779909 61779909 61779909 TTTGTATTTTTAGTAGAGTTGGGGGTTTCTCCATGTTCACCAGGCTGGTCTTGAACTCCCGATCT TTTGTATTTTTAGTAGAGTTGGGGGTTTCTCCGTGTTCACCAGGCTGGTCTTGAACTCCCGATCT A G SNAPC1 Ensembl:ENSG00000023608 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971382149 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167129,RMVar_hsa_circ_337720,RMVar_hsa_circ_90192,RMVar_hsa_circ_7503,RMVar_hsa_circ_313123,RMVar_hsa_circ_284957,RMVar_hsa_circ_167131 16455 RMVar_ID_16455 Human_SNP_ID_557654479 A-to-I Human chr14 + 61782772 61782772 61782772 TTTCTACTAAAAATATAAAAGTCGGGCATGGTAGCGCATGCCTGTAATCCCAGCTACTTGGGAGG TTTCTACTAAAAATATAAAAGTCGGGCATGGTCGCGCATGCCTGTAATCCCAGCTACTTGGGAGG A C SNAPC1 Ensembl:ENSG00000023608 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1347931034 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167129,RMVar_hsa_circ_90192,RMVar_hsa_circ_7503 16456 RMVar_ID_16456 Human_SNP_ID_557654871 A-to-I Human chr14 + 61783749 61783749 61783749 TTTAGTAGAGACGGGGTTTCACTATGTTGGCCAGGCTGGTCTTGAACTCCTGACTTCGTGATTCG TTTAGTAGAGACGGGGTTTCACTATGTTGGCCGGGCTGGTCTTGAACTCCTGACTTCGTGATTCG A G SNAPC1 Ensembl:ENSG00000023608 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903638679 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167129,RMVar_hsa_circ_90192,RMVar_hsa_circ_7503 16457 RMVar_ID_16457 Human_SNP_ID_557656672 A-to-I Human chr14 + 61790589 61790589 61790589 GAACTCCTGACGTTAAATAATCCACCCACCTCAGCCTCCTAAAGTGCTGAGATTACAGGCGCAAG GAACTCCTGACGTTAAATAATCCACCCACCTCGGCCTCCTAAAGTGCTGAGATTACAGGCGCAAG A G SNAPC1 Ensembl:ENSG00000023608 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1158117763 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167129,RMVar_hsa_circ_90192,RMVar_hsa_circ_7503 16458 RMVar_ID_16458 Human_SNP_ID_557658184 A-to-I Human chr14 + 61795946 61795946 61795946 GAACTCCTGGGCTCAAGCTATCCTCCTGCCTCAGCCTCCCAAAGTACTGGGATTATAGGTGTGAG GAACTCCTGGGCTCAAGCTATCCTCCTGCCTCGGCCTCCCAAAGTACTGGGATTATAGGTGTGAG A G SNAPC1 Ensembl:ENSG00000023608 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490832,GSM3490833,GSM3490834 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 31158229,32596459 RNA-Seq:(High) rs1053513057 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_449450 RMVar_hsa_circ_167129,RMVar_hsa_circ_90192 16459 RMVar_ID_16459 Human_SNP_ID_557992948 A-to-I Human chr14 - 63123071 63123071 63123071 TCCCTTTACCAAACATGTAGCCCGTCATGGGCACTTCAGGCGGGGCTATCCAAAGACCCTGGGAC TCCCTTTACCAAACATGTAGCCCGTCATGGGCGCTTCAGGCGGGGCTATCCAAAGACCCTGGGAC T C AL137191.1 Ensembl:ENSG00000259093 lincRNA exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs878933652 Functional Loss SNV dbSNP153 33..33 33 - - - 16460 RMVar_ID_16460 Human_SNP_ID_557993030 A-to-I Human chr14 - 63123365 63123365 63123365 TCATAGACAATGTACTCATTATATAGTAGACAAGTGTCATTCACACCAGATGAAATCCCAGTCCC TCATAGACAATGTACTCATTATATAGTAGACAGGTGTCATTCACACCAGATGAAATCCCAGTCCC T C AL137191.1 Ensembl:ENSG00000259093 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs943085298 Functional Loss SNV dbSNP153 33..33 33 - - - 16461 RMVar_ID_16461 Human_SNP_ID_558055305 A-to-I Human chr14 - 63385282 63385282 63385282 TTGCTCTGTCACCCAAGCTGGAGTTCAGTGGCATGATCTCCACTCACTGCAACCTCCGCCTCCCA TTGCTCTGTCACCCAAGCTGGAGTTCAGTGGCGTGATCTCCACTCACTGCAACCTCCGCCTCCCA T C PPP2R5E Ensembl:ENSG00000154001 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1403412460 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63842 16462 RMVar_ID_16462 Human_SNP_ID_558083208 A-to-I Human chr14 - 63495837 63495837 63495837 AAATCAAAGAAACTAGCTGGGCAAGGTGGTACATGCCTGTTTTCTCAGTTACTTGGGAGGCTGAG AAATCAAAGAAACTAGCTGGGCAAGGTGGTACGTGCCTGTTTTCTCAGTTACTTGGGAGGCTGAG T C PPP2R5E Ensembl:ENSG00000154001 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs772751718 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12378869 RMVar_hsa_circ_23038,RMVar_hsa_circ_20209 16463 RMVar_ID_16463 Human_SNP_ID_558083213 A-to-I Human chr14 - 63495846 63495846 63495846 TCTCTACAAAAATCAAAGAAACTAGCTGGGCAAGGTGGTACATGCCTGTTTTCTCAGTTACTTGG TCTCTACAAAAATCAAAGAAACTAGCTGGGCAGGGTGGTACATGCCTGTTTTCTCAGTTACTTGG T C PPP2R5E Ensembl:ENSG00000154001 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1376376385 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12378869 RMVar_hsa_circ_23038,RMVar_hsa_circ_20209 16464 RMVar_ID_16464 Human_SNP_ID_558083217 A-to-I Human chr14 - 63495863 63495863 63495863 AACATAGGGAAACCTTGTCTCTACAAAAATCAAAGAAACTAGCTGGGCAAGGTGGTACATGCCTG AACATAGGGAAACCTTGTCTCTACAAAAATCAGAGAAACTAGCTGGGCAAGGTGGTACATGCCTG T C PPP2R5E Ensembl:ENSG00000154001 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs765924481 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6368552,Human_RBP_ID_18653503 RMVar_hsa_circ_23038,RMVar_hsa_circ_20209 16465 RMVar_ID_16465 Human_SNP_ID_558088723 A-to-I Human chr14 - 63518338 63518338 63518338 ACTCCAGAGGCTAAGGCAGGAGGATCCCTTGAACCCAGGAGTTTGAGGCTGCAGTTAACCATGAT ACTCCAGAGGCTAAGGCAGGAGGATCCCTTGAGCCCAGGAGTTTGAGGCTGCAGTTAACCATGAT T C PPP2R5E Ensembl:ENSG00000154001 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1263141452 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23038,RMVar_hsa_circ_20209 16466 RMVar_ID_16466 Human_SNP_ID_558092716 A-to-I Human chr14 - 63531121 63531121 63531121 TCTTGTTGCCCAGGCTGGAGCGCAATGGCGCTATCTTGGCTCTCTGCAACCTCCGCCTCCCGAGT TCTTGTTGCCCAGGCTGGAGCGCAATGGCGCTGTCTTGGCTCTCTGCAACCTCCGCCTCCCGAGT T C PPP2R5E Ensembl:ENSG00000154001 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1165277310 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12379530,Human_RBP_ID_25106596 RMVar_hsa_circ_23038,RMVar_hsa_circ_20209 16467 RMVar_ID_16467 Human_SNP_ID_558092717 A-to-I Human chr14 - 63531121 63531121 63531121 TCTTGTTGCCCAGGCTGGAGCGCAATGGCGCTATCTTGGCTCTCTGCAACCTCCGCCTCCCGAGT TCTTGTTGCCCAGGCTGGAGCGCAATGGCGCTCTCTTGGCTCTCTGCAACCTCCGCCTCCCGAGT T G PPP2R5E Ensembl:ENSG00000154001 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1165277310 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12379530,Human_RBP_ID_25106596 RMVar_hsa_circ_23038,RMVar_hsa_circ_20209 16468 RMVar_ID_16468 Human_SNP_ID_558093772 A-to-I Human chr14 - 63535310 63535310 63535310 TCAAGTGATTCTCTTGCCTCAGGCTCCTGAGTAGCTGGGATTGCAGGTGCCCACCACCACACCAA TCAAGTGATTCTCTTGCCTCAGGCTCCTGAGTTGCTGGGATTGCAGGTGCCCACCACCACACCAA T A PPP2R5E Ensembl:ENSG00000154001 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1315894446 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23038,RMVar_hsa_circ_20209 16469 RMVar_ID_16469 Human_SNP_ID_558109327 A-to-I Human chr14 + 63594172 63594172 63594172 CCCTTGGAGACCACAGGGTAGCTGAACCCAATAACAAAGATGCCTCTCTTCAGCATGTCATCCGC CCCTTGGAGACCACAGGGTAGCTGAACCCAATCACAAAGATGCCTCTCTTCAGCATGTCATCCGC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1468685767 Functional Loss SNV dbSNP153 33..33 33 - - - 16470 RMVar_ID_16470 Human_SNP_ID_558111371 A-to-I Human chr14 - 63601697 63601697 63601697 TATGGGAGAAGAACTTTATCTCCAACTTTCACACGAACTGGTTGAATCTCTCCACCCTTTCCTTT TATGGGAGAAGAACTTTATCTCCAACTTTCACGCGAACTGGTTGAATCTCTCCACCCTTTCCTTT T C WDR89 Ensembl:ENSG00000140006 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs546819518 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120390,RMVar_hsa_circ_167171 16471 RMVar_ID_16471 Human_SNP_ID_558113916 A-to-I Human chr14 - 63610967 63610967 63610967 AGCCAGGCACAGTGGCTCATGCCTATAACCCCAGCACTTTGGGAGGCCAAGGCGGGCGAATTACA AGCCAGGCACAGTGGCTCATGCCTATAACCCCCGCACTTTGGGAGGCCAAGGCGGGCGAATTACA T G WDR89 Ensembl:ENSG00000140006 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs940010152 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120390,RMVar_hsa_circ_167171 16472 RMVar_ID_16472 Human_SNP_ID_558113949 A-to-I Human chr14 - 63611104 63611104 63611104 TCAAACTCTTGGCCTCAAGATCTGCCTGTCTCAGCCTCCCCGAGTGCTAGGATTGCAGGCATGAG TCAAACTCTTGGCCTCAAGATCTGCCTGTCTCGGCCTCCCCGAGTGCTAGGATTGCAGGCATGAG T C WDR89 Ensembl:ENSG00000140006 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs55837988 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120390,RMVar_hsa_circ_167171 16473 RMVar_ID_16473 Human_SNP_ID_558119264 A-to-I Human chr14 - 63630869 63630869 63630869 CAGGAGGCTGGGGTGGGAGGATTGAGACTGCAATGAGCTGTGTTTGTGCCACTACACTGCATCCT CAGGAGGCTGGGGTGGGAGGATTGAGACTGCATTGAGCTGTGTTTGTGCCACTACACTGCATCCT T A WDR89 Ensembl:ENSG00000140006 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs562229972 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120390,RMVar_hsa_circ_167171 16474 RMVar_ID_16474 Human_SNP_ID_558119265 A-to-I Human chr14 - 63630869 63630869 63630869 CAGGAGGCTGGGGTGGGAGGATTGAGACTGCAATGAGCTGTGTTTGTGCCACTACACTGCATCCT CAGGAGGCTGGGGTGGGAGGATTGAGACTGCAGTGAGCTGTGTTTGTGCCACTACACTGCATCCT T C WDR89 Ensembl:ENSG00000140006 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs562229972 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120390,RMVar_hsa_circ_167171 16475 RMVar_ID_16475 Human_SNP_ID_558124973 A-to-I Human chr14 + 63653091 63653091 63653091 TAATTTTTGTATTTTTAGTAGAGTTTCATCATATTGGTCAGACTGGTCTCGAACTCCTGACCTCA TAATTTTTGTATTTTTAGTAGAGTTTCATCATGTTGGTCAGACTGGTCTCGAACTCCTGACCTCA A G AL136038.7 Ensembl:ENSG00000274015 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs925386493 Functional Loss SNV dbSNP153 33..33 33 - - - 16476 RMVar_ID_16476 Human_SNP_ID_558125163 A-to-I Human chr14 + 63653839 63653839 63653839 TGGGGGATGAGGCAGGAGGATTGCTTGAGCCCAGGAGGCGGAGGTTGCAGTGAGCCCAGATCTCT TGGGGGATGAGGCAGGAGGATTGCTTGAGCCCGGGAGGCGGAGGTTGCAGTGAGCCCAGATCTCT A G AL136038.7 Ensembl:ENSG00000274015 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1408940104 Functional Loss SNV dbSNP153 33..33 33 - - - 16477 RMVar_ID_16477 Human_SNP_ID_558132875 A-to-I Human chr14 - 63685798 63685798 63685798 TATAATATATATAAGGTACATAATATGCAATTATATATCTGATATATATTATATATAAAATAATA TATAATATATATAAGGTACATAATATGCAATTGTATATCTGATATATATTATATATAAAATAATA T C SGPP1 Ensembl:ENSG00000126821 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1173287635 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1116994,Human_miRNA_ID_1124186,Human_miRNA_ID_1210704 16478 RMVar_ID_16478 Human_SNP_ID_558133255 A-to-I Human chr14 - 63687218 63687217 63687219 CAGGCTGGTCTTGAACTCCTGGCCTCAAGTGAACCACCCACCTCAGCCTCCCAAAGGGATGGGAT CAGGCTGGTCTTGAACTCCTGGCCTCAAGTG__CCACCCACCTCAGCCTCCCAAAGGGATGGGAT GTT G SGPP1 Ensembl:ENSG00000126821 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017210015 Functional Loss DEL dbSNP153 32..33 33 - - - 16479 RMVar_ID_16479 Human_SNP_ID_558133287 A-to-I Human chr14 - 63687357 63687357 63687357 TGGCTCACTGCAACCTCCACTTCCTGGGTTCAAGCGATTCTCATGCCTCCATCCCCAAGTAGCTG TGGCTCACTGCAACCTCCACTTCCTGGGTTCAGGCGATTCTCATGCCTCCATCCCCAAGTAGCTG T C SGPP1 Ensembl:ENSG00000126821 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1296618909 Functional Loss SNV dbSNP153 33..33 33 - - - 16480 RMVar_ID_16480 Human_SNP_ID_558134224 A-to-I Human chr14 - 63690839 63690839 63690839 GTGGTTGGTGGCGCACACCTGTAACCCCAGCTACTTGGGAGGCTGAGACAGGAGAATTGCTTGAA GTGGTTGGTGGCGCACACCTGTAACCCCAGCTGCTTGGGAGGCTGAGACAGGAGAATTGCTTGAA T C SGPP1 Ensembl:ENSG00000126821 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs747552362 Functional Loss SNV dbSNP153 33..33 33 - - - 16481 RMVar_ID_16481 Human_SNP_ID_558134238 A-to-I Human chr14 - 63690888 63690888 63690888 CAACATGGTGAAACCCTGTCTGTACTAAAAATACAAAAATTAGCTGAGTGTGGTTGGTGGCGCAC CAACATGGTGAAACCCTGTCTGTACTAAAAATGCAAAAATTAGCTGAGTGTGGTTGGTGGCGCAC T C SGPP1 Ensembl:ENSG00000126821 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1011558767 Functional Loss SNV dbSNP153 33..33 33 - - - 16482 RMVar_ID_16482 Human_SNP_ID_558134616 A-to-I Human chr14 - 63692727 63692727 63692727 AGTGTTGAGGCTGGATGTGGTGGATAATGCCTATAATTCCAACACTTTGGGAAGCTGAGGTGGGT AGTGTTGAGGCTGGATGTGGTGGATAATGCCTGTAATTCCAACACTTTGGGAAGCTGAGGTGGGT T C SGPP1 Ensembl:ENSG00000126821 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1210928723 Functional Loss SNV dbSNP153 33..33 33 - - - 16483 RMVar_ID_16483 Human_SNP_ID_558134828 A-to-I Human chr14 - 63693687 63693687 63693687 ATTGCTTGAGCCAGGAAGATTGAGGCTGCAATAAGCTGTGATTTTGCCACTGTACTCCAGCCTGG ATTGCTTGAGCCAGGAAGATTGAGGCTGCAATGAGCTGTGATTTTGCCACTGTACTCCAGCCTGG T C SGPP1 Ensembl:ENSG00000126821 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1018249794 Functional Loss SNV dbSNP153 33..33 33 - - - 16484 RMVar_ID_16484 Human_SNP_ID_558134882 A-to-I Human chr14 - 63693873 63693873 63693873 AAATACCTGGCTGGGCACAGCAGCCCACGCCTATAATCCCAACAATTTGCAAGGCCAAGGTGGGA AAATACCTGGCTGGGCACAGCAGCCCACGCCTGTAATCCCAACAATTTGCAAGGCCAAGGTGGGA T C SGPP1 Ensembl:ENSG00000126821 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs941968338 Functional Loss SNV dbSNP153 33..33 33 - - - 16485 RMVar_ID_16485 Human_SNP_ID_558134989 A-to-I Human chr14 - 63694211 63694211 63694211 GGAGTGCAGTGGCGTAATCTCTGCTCACTGCAACCTTTGCCTCCTGGACTCAAGCGATCTTCCCA GGAGTGCAGTGGCGTAATCTCTGCTCACTGCAGCCTTTGCCTCCTGGACTCAAGCGATCTTCCCA T C SGPP1 Ensembl:ENSG00000126821 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1369262152 Functional Loss SNV dbSNP153 33..33 33 - - - 16486 RMVar_ID_16486 Human_SNP_ID_558135370 A-to-I Human chr14 - 63695676 63695676 63695676 AAACTCCTGGTTCAAGTGATCGTTCCACCTCAACCTCTCAAGGTGCTGGGATTACAGATGTGAGC AAACTCCTGGTTCAAGTGATCGTTCCACCTCAGCCTCTCAAGGTGCTGGGATTACAGATGTGAGC T C SGPP1 Ensembl:ENSG00000126821 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs528257504 Functional Loss SNV dbSNP153 33..33 33 - - - 16487 RMVar_ID_16487 Human_SNP_ID_558135399 A-to-I Human chr14 - 63695786 63695786 63695786 CCACCTTACCCTCCCGGGTGTCTAGGACTACAAACATGTACTATAATGCCCAGCTAATTTTTAAA CCACCTTACCCTCCCGGGTGTCTAGGACTACAGACATGTACTATAATGCCCAGCTAATTTTTAAA T C SGPP1 Ensembl:ENSG00000126821 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1214873489 Functional Loss SNV dbSNP153 33..33 33 - - - 16488 RMVar_ID_16488 Human_SNP_ID_558135403 A-to-I Human chr14 - 63695795 63695795 63695795 GTGATCCTCCCACCTTACCCTCCCGGGTGTCTAGGACTACAAACATGTACTATAATGCCCAGCTA GTGATCCTCCCACCTTACCCTCCCGGGTGTCTGGGACTACAAACATGTACTATAATGCCCAGCTA T C SGPP1 Ensembl:ENSG00000126821 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1287123868 Functional Loss SNV dbSNP153 33..33 33 - - - 16489 RMVar_ID_16489 Human_SNP_ID_558140277 A-to-I Human chr14 - 63715178 63715173 63715178 AAACCCTGTCTCTACTAAAAATACAAACAATTAGCTGGGCGTGGTGGCAGGCGCCTGTAATCCCA AAACCCTGTCTCTACTAAAAATACAAACAATT_____GGCGTGGTGGCAGGCGCCTGTAATCCCA CCAGCT C SGPP1 Ensembl:ENSG00000126821 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs902617675 Functional Loss DEL dbSNP153 33..37 33 - - - Human_RBP_ID_121453 16490 RMVar_ID_16490 Human_SNP_ID_558142675 A-to-I Human chr14 - 63723636 63723636 63723636 TGTCTCACTGCAAACTCTGCCTCCCCGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTCAGTAGCT TGTCTCACTGCAAACTCTGCCTCCCCGGTTCAGGCGATTCTCCTGCCTCAGCCTCCTCAGTAGCT T C SGPP1 Ensembl:ENSG00000126821 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs994344496 Functional Loss SNV dbSNP153 33..33 33 - - - 16491 RMVar_ID_16491 Human_SNP_ID_558142682 A-to-I Human chr14 - 63723656 63723656 63723656 GGAGTGTGGTGGTGTGATCTTGTCTCACTGCAAACTCTGCCTCCCCGGTTCAAGCGATTCTCCTG GGAGTGTGGTGGTGTGATCTTGTCTCACTGCAGACTCTGCCTCCCCGGTTCAAGCGATTCTCCTG T C SGPP1 Ensembl:ENSG00000126821 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1197770107 Functional Loss SNV dbSNP153 33..33 33 - - - 16492 RMVar_ID_16492 Human_SNP_ID_558142754 A-to-I Human chr14 - 63724016 63724016 63724016 AAAATCAGCTGGGCATGGTGGCGCATGCCTGTAGTTCTAGCTACTAGGGAGGCTGAGGTGGGAGC AAAATCAGCTGGGCATGGTGGCGCATGCCTGTGGTTCTAGCTACTAGGGAGGCTGAGGTGGGAGC T C SGPP1 Ensembl:ENSG00000126821 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs137968210 Functional Loss SNV dbSNP153 33..33 33 - - - 16493 RMVar_ID_16493 Human_SNP_ID_558176451 A-to-I Human chr14 + 63856808 63856808 63856808 TATTTTATTTTTTTGAGACAAGGTCTCGTTCTATCACCCAGGCTGGAGTACAGTGGTGCGATCAT TATTTTATTTTTTTGAGACAAGGTCTCGTTCTGTCACCCAGGCTGGAGTACAGTGGTGCGATCAT A G SYNE2 Ensembl:ENSG00000054654 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs554745444 Functional Loss SNV dbSNP153 33..33 33 - - - 16494 RMVar_ID_16494 Human_SNP_ID_558176452 A-to-I Human chr14 + 63856808 63856808 63856808 TATTTTATTTTTTTGAGACAAGGTCTCGTTCTATCACCCAGGCTGGAGTACAGTGGTGCGATCAT TATTTTATTTTTTTGAGACAAGGTCTCGTTCTTTCACCCAGGCTGGAGTACAGTGGTGCGATCAT A T SYNE2 Ensembl:ENSG00000054654 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs554745444 Functional Loss SNV dbSNP153 33..33 33 - - - 16495 RMVar_ID_16495 Human_SNP_ID_558176469 A-to-I Human chr14 + 63856871 63856871 63856871 ATGGCTCACTGTAGCCTCTACCTCCTGGGCCCAAGTGATTCTCCCACCCCGGCCTCCCAAGTAAC ATGGCTCACTGTAGCCTCTACCTCCTGGGCCCGAGTGATTCTCCCACCCCGGCCTCCCAAGTAAC A G SYNE2 Ensembl:ENSG00000054654 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1434258457 Functional Loss SNV dbSNP153 33..33 33 - - - 16496 RMVar_ID_16496 Human_SNP_ID_558177605 A-to-I Human chr14 + 63861244 63861244 63861244 TCAGCTCACTGCAACCTTCGCCTCCTGGGTTCAAGCGATTATCCTACCTCAGACTCCTGAGTAGC TCAGCTCACTGCAACCTTCGCCTCCTGGGTTCCAGCGATTATCCTACCTCAGACTCCTGAGTAGC A C SYNE2 Ensembl:ENSG00000054654 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs188357709 Functional Loss SNV dbSNP153 33..33 33 - - - 16497 RMVar_ID_16497 Human_SNP_ID_558179203 A-to-I Human chr14 + 63867514 63867514 63867514 GAGGTCAGGAATTCGACACCAGCCCGGCCAACAAGGCTAAACCTTGTCTCTACTAAAAATACAAA GAGGTCAGGAATTCGACACCAGCCCGGCCAACGAGGCTAAACCTTGTCTCTACTAAAAATACAAA A G SYNE2 Ensembl:ENSG00000054654 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1566654946 Functional Loss SNV dbSNP153 33..33 33 - - - 16498 RMVar_ID_16498 Human_SNP_ID_558180516 A-to-I Human chr14 + 63872498 63872498 63872498 GTCTAATTGGCTGGGCATGGTGGCTCACACCTATAATCCCAGCACTTTGGGAGGCCGAGGCGAGT GTCTAATTGGCTGGGCATGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGAGT A G SYNE2 Ensembl:ENSG00000054654 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982310616 Functional Loss SNV dbSNP153 33..33 33 - - - 16499 RMVar_ID_16499 Human_SNP_ID_558181505 A-to-I Human chr14 + 63876348 63876348 63876348 CTGAGGTGGAGCCAGAAGTTCAAGGCTGTAGTAAGCTATGATCATACTGCTAAACTCCAGCCTGG CTGAGGTGGAGCCAGAAGTTCAAGGCTGTAGTGAGCTATGATCATACTGCTAAACTCCAGCCTGG A G SYNE2 Ensembl:ENSG00000054654 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1349809599 Functional Loss SNV dbSNP153 33..33 33 - - - 16500 RMVar_ID_16500 Human_SNP_ID_558182103 A-to-I Human chr14 + 63878723 63878723 63878723 TGCCATCAGGCCTGGCTAAATTTTGTATTTTTAGTAGAGATGAGGTTTCATCATGTTGGTTAGCC TGCCATCAGGCCTGGCTAAATTTTGTATTTTTGGTAGAGATGAGGTTTCATCATGTTGGTTAGCC A G SYNE2 Ensembl:ENSG00000054654 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs558598627 Functional Loss SNV dbSNP153 33..33 33 - - - 16501 RMVar_ID_16501 Human_SNP_ID_558182747 A-to-I Human chr14 + 63881390 63881390 63881390 ATTGCTATAGAATAAAAATTTGGGCCAGGCACAGTGGCTTACGGCTGTAATCCCAGCACTTTGGG ATTGCTATAGAATAAAAATTTGGGCCAGGCACGGTGGCTTACGGCTGTAATCCCAGCACTTTGGG A G SYNE2 Ensembl:ENSG00000054654 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1207672405 Functional Loss SNV dbSNP153 33..33 33 - - - 16502 RMVar_ID_16502 Human_SNP_ID_558185673 A-to-I Human chr14 + 63893457 63893457 63893457 GGGCGTGGTGGCACACGCCTGTAGTCCCATCTACTCAGGAGGCTGAGGTGGATCACTTGAGCCTG GGGCGTGGTGGCACACGCCTGTAGTCCCATCTCCTCAGGAGGCTGAGGTGGATCACTTGAGCCTG A C SYNE2 Ensembl:ENSG00000054654 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984421919 Functional Loss SNV dbSNP153 33..33 33 - - - 16503 RMVar_ID_16503 Human_SNP_ID_558185674 A-to-I Human chr14 + 63893457 63893457 63893457 GGGCGTGGTGGCACACGCCTGTAGTCCCATCTACTCAGGAGGCTGAGGTGGATCACTTGAGCCTG GGGCGTGGTGGCACACGCCTGTAGTCCCATCTGCTCAGGAGGCTGAGGTGGATCACTTGAGCCTG A G SYNE2 Ensembl:ENSG00000054654 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984421919 Functional Loss SNV dbSNP153 33..33 33 - - - 16504 RMVar_ID_16504 Human_SNP_ID_558185685 A-to-I Human chr14 + 63893508 63893508 63893508 ATCACTTGAGCCTGGGAGGTTGAGGCTGCAGTAAGGTAAGATCGTGCCACTGTACTCCAGCCTGG ATCACTTGAGCCTGGGAGGTTGAGGCTGCAGTGAGGTAAGATCGTGCCACTGTACTCCAGCCTGG A G SYNE2 Ensembl:ENSG00000054654 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202055482 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8407007 16505 RMVar_ID_16505 Human_SNP_ID_558198512 A-to-I Human chr14 + 63946410 63946410 63946410 TGACTGGGCTACTGCACTCTAGCCTGGGCAACAGAGCAAGACCCTGTCTCCAAAAAACATACACA TGACTGGGCTACTGCACTCTAGCCTGGGCAACCGAGCAAGACCCTGTCTCCAAAAAACATACACA A C SYNE2 Ensembl:ENSG00000054654 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs926304358 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2286,RMVar_hsa_circ_47848,RMVar_hsa_circ_284638,RMVar_hsa_circ_285020,RMVar_hsa_circ_66647,RMVar_hsa_circ_32876,RMVar_hsa_circ_44029,RMVar_hsa_circ_25844,RMVar_hsa_circ_63876,RMVar_hsa_circ_265369,RMVar_hsa_circ_167175,RMVar_hsa_circ_100075,RMVar_hsa_circ_167180,RMVar_hsa_circ_46232,RMVar_hsa_circ_167179 16506 RMVar_ID_16506 Human_SNP_ID_558198513 A-to-I Human chr14 + 63946415 63946415 63946415 GGGCTACTGCACTCTAGCCTGGGCAACAGAGCAAGACCCTGTCTCCAAAAAACATACACATACAC GGGCTACTGCACTCTAGCCTGGGCAACAGAGCGAGACCCTGTCTCCAAAAAACATACACATACAC A G SYNE2 Ensembl:ENSG00000054654 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1247097099 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2286,RMVar_hsa_circ_47848,RMVar_hsa_circ_284638,RMVar_hsa_circ_285020,RMVar_hsa_circ_66647,RMVar_hsa_circ_32876,RMVar_hsa_circ_44029,RMVar_hsa_circ_25844,RMVar_hsa_circ_63876,RMVar_hsa_circ_265369,RMVar_hsa_circ_167175,RMVar_hsa_circ_100075,RMVar_hsa_circ_167180,RMVar_hsa_circ_46232,RMVar_hsa_circ_167179 16507 RMVar_ID_16507 Human_SNP_ID_558209287 A-to-I Human chr14 + 63985865 63985865 63985865 ACCCCATCTCTACAAAATATAAAAACTTAGCTAGACGTAGTGGCATACACCTGTAATTCCAGCCA ACCCCATCTCTACAAAATATAAAAACTTAGCTGGACGTAGTGGCATACACCTGTAATTCCAGCCA A G SYNE2 Ensembl:ENSG00000054654 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1322341143 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2286,RMVar_hsa_circ_32876,RMVar_hsa_circ_44029,RMVar_hsa_circ_46232,RMVar_hsa_circ_12081,RMVar_hsa_circ_7938,RMVar_hsa_circ_17747,RMVar_hsa_circ_62730,RMVar_hsa_circ_23278,RMVar_hsa_circ_40763,RMVar_hsa_circ_79960,RMVar_hsa_circ_48806,RMVar_hsa_circ_67055,RMVar_hsa_circ_167186,RMVar_hsa_circ_321060,RMVar_hsa_circ_66799,RMVar_hsa_circ_36926,RMVar_hsa_circ_269007,RMVar_hsa_circ_355081,RMVar_hsa_circ_167187,RMVar_hsa_circ_325406,RMVar_hsa_circ_62145,RMVar_hsa_circ_272857,RMVar_hsa_circ_167188,RMVar_hsa_circ_167189,RMVar_hsa_circ_338972 16508 RMVar_ID_16508 Human_SNP_ID_558220251 A-to-I Human chr14 + 64028444 64028444 64028444 CACCCAGCTAATTTTTTTATTTTTGTAGAAATAAGGTCTCGCTTTGTTGCCCAAGCTGGTCTAGA CACCCAGCTAATTTTTTTATTTTTGTAGAAATGAGGTCTCGCTTTGTTGCCCAAGCTGGTCTAGA A G SYNE2 Ensembl:ENSG00000054654 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1469309083 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44029,RMVar_hsa_circ_79960,RMVar_hsa_circ_167186,RMVar_hsa_circ_66799,RMVar_hsa_circ_269007,RMVar_hsa_circ_2670,RMVar_hsa_circ_59545,RMVar_hsa_circ_5287,RMVar_hsa_circ_346856,RMVar_hsa_circ_321136,RMVar_hsa_circ_72238,RMVar_hsa_circ_67824,RMVar_hsa_circ_48442,RMVar_hsa_circ_13560,RMVar_hsa_circ_167193,RMVar_hsa_circ_25139,RMVar_hsa_circ_84310,RMVar_hsa_circ_167203,RMVar_hsa_circ_49613,RMVar_hsa_circ_365122,RMVar_hsa_circ_360069,RMVar_hsa_circ_333124,RMVar_hsa_circ_33615,RMVar_hsa_circ_42824 16509 RMVar_ID_16509 Human_SNP_ID_558227073 A-to-I Human chr14 + 64053854 64053854 64053854 AGCTGGGTATGGTGGCACATGGTTGTAATCCCAGCTACTCAGGAGGCTGAGGTACAAGAATCACT AGCTGGGTATGGTGGCACATGGTTGTAATCCCGGCTACTCAGGAGGCTGAGGTACAAGAATCACT A G SYNE2 Ensembl:ENSG00000054654 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs112071840 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44029,RMVar_hsa_circ_79960,RMVar_hsa_circ_167186,RMVar_hsa_circ_2670,RMVar_hsa_circ_59545,RMVar_hsa_circ_5287,RMVar_hsa_circ_321136,RMVar_hsa_circ_67824,RMVar_hsa_circ_48442,RMVar_hsa_circ_13560,RMVar_hsa_circ_167193,RMVar_hsa_circ_84310,RMVar_hsa_circ_167203,RMVar_hsa_circ_13466,RMVar_hsa_circ_49613,RMVar_hsa_circ_360069,RMVar_hsa_circ_33615,RMVar_hsa_circ_42824,RMVar_hsa_circ_338120,RMVar_hsa_circ_303135,RMVar_hsa_circ_18826,RMVar_hsa_circ_167206 16510 RMVar_ID_16510 Human_SNP_ID_558227494 A-to-I Human chr14 + 64055566 64055566 64055566 AATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATACTGGCCAGGCTGGTCTTGAACTCTGGA AATTTTTGTATTTTTAGTAGAGATGGGGTTTCGCCATACTGGCCAGGCTGGTCTTGAACTCTGGA A G SYNE2 Ensembl:ENSG00000054654 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs979594496 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44029,RMVar_hsa_circ_79960,RMVar_hsa_circ_167186,RMVar_hsa_circ_2670,RMVar_hsa_circ_59545,RMVar_hsa_circ_5287,RMVar_hsa_circ_321136,RMVar_hsa_circ_67824,RMVar_hsa_circ_48442,RMVar_hsa_circ_13560,RMVar_hsa_circ_167193,RMVar_hsa_circ_84310,RMVar_hsa_circ_167203,RMVar_hsa_circ_13466,RMVar_hsa_circ_49613,RMVar_hsa_circ_360069,RMVar_hsa_circ_33615,RMVar_hsa_circ_42824,RMVar_hsa_circ_338120,RMVar_hsa_circ_303135,RMVar_hsa_circ_18826,RMVar_hsa_circ_167206 16511 RMVar_ID_16511 Human_SNP_ID_558243089 A-to-I Human chr14 + 64116050 64116049 64116050 TAAACTAGCTGGGCATGGTGGTGTGTATCTGTAGTCCCAGCTACCTGGGAGGCTGAGGCACTAAT TAAACTAGCTGGGCATGGTGGTGTGTATCTGT_GTCCCAGCTACCTGGGAGGCTGAGGCACTAAT TA T SYNE2 Ensembl:ENSG00000054654 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1332901923 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_44029,RMVar_hsa_circ_79960,RMVar_hsa_circ_167186,RMVar_hsa_circ_59545,RMVar_hsa_circ_5287,RMVar_hsa_circ_48442,RMVar_hsa_circ_84310,RMVar_hsa_circ_167203,RMVar_hsa_circ_360069,RMVar_hsa_circ_21339,RMVar_hsa_circ_61086,RMVar_hsa_circ_265457,RMVar_hsa_circ_50004,RMVar_hsa_circ_10721,RMVar_hsa_circ_27978,RMVar_hsa_circ_71901,RMVar_hsa_circ_296543,RMVar_hsa_circ_34563,RMVar_hsa_circ_167218,RMVar_hsa_circ_349220,RMVar_hsa_circ_60000,RMVar_hsa_circ_321297,RMVar_hsa_circ_111404,RMVar_hsa_circ_167221,RMVar_hsa_circ_167222,RMVar_hsa_circ_128179,RMVar_hsa_circ_167224,RMVar_hsa_circ_82229,RMVar_hsa_circ_167225,RMVar_hsa_circ_167223 16512 RMVar_ID_16512 Human_SNP_ID_558254211 A-to-I Human chr14 + 64155082 64155082 64155082 AGAGTCTGGCAGTTCCTCAAATGGTTAAACATAAAGTTACCATGCAACTTAGCAGTTCTACTCCT AGAGTCTGGCAGTTCCTCAAATGGTTAAACATGAAGTTACCATGCAACTTAGCAGTTCTACTCCT A G SYNE2 Ensembl:ENSG00000054654 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs916220647 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44029,RMVar_hsa_circ_79960,RMVar_hsa_circ_167186,RMVar_hsa_circ_84310,RMVar_hsa_circ_167203,RMVar_hsa_circ_27022,RMVar_hsa_circ_128179,RMVar_hsa_circ_167225,RMVar_hsa_circ_350730,RMVar_hsa_circ_167226,RMVar_hsa_circ_91910,RMVar_hsa_circ_167230,RMVar_hsa_circ_54670,RMVar_hsa_circ_64426 16513 RMVar_ID_16513 Human_SNP_ID_558254424 A-to-I Human chr14 + 64155781 64155781 64155781 AGATCCCATCTCCACAAAAAGTAAATAAAGTTAGCCGGATGTGGTGGCATGCACCTGTAATCCCA AGATCCCATCTCCACAAAAAGTAAATAAAGTTCGCCGGATGTGGTGGCATGCACCTGTAATCCCA A C SYNE2 Ensembl:ENSG00000054654 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs143992131 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44029,RMVar_hsa_circ_79960,RMVar_hsa_circ_167186,RMVar_hsa_circ_84310,RMVar_hsa_circ_167203,RMVar_hsa_circ_27022,RMVar_hsa_circ_128179,RMVar_hsa_circ_167225,RMVar_hsa_circ_350730,RMVar_hsa_circ_167226,RMVar_hsa_circ_91910,RMVar_hsa_circ_167230,RMVar_hsa_circ_54670,RMVar_hsa_circ_64426 16514 RMVar_ID_16514 Human_SNP_ID_558306790 A-to-I Human chr14 - 64352227 64352227 64352227 ACCATCACGATTCACTGTAGCCTCAACCTCCTAAGGCTCAAGTGCTCCTCTTGCCTCAGACTCCC ACCATCACGATTCACTGTAGCCTCAACCTCCTGAGGCTCAAGTGCTCCTCTTGCCTCAGACTCCC T C TEX21P,AL161756.3 Ensembl:ENSG00000234911,Ensembl:ENSG00000284664 Pseudogene,lincRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1035928223 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_449665,Human_RBP_ID_5246766 16515 RMVar_ID_16515 Human_SNP_ID_558306798 A-to-I Human chr14 - 64352259 64352259 64352259 TTGCTCTGCCTCCCAGGCTGGAATGTGGTGTTACCATCACGATTCACTGTAGCCTCAACCTCCTA TTGCTCTGCCTCCCAGGCTGGAATGTGGTGTTTCCATCACGATTCACTGTAGCCTCAACCTCCTA T A TEX21P,AL161756.3 Ensembl:ENSG00000234911,Ensembl:ENSG00000284664 Pseudogene,lincRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256567543 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5246766 16516 RMVar_ID_16516 Human_SNP_ID_558315313 A-to-I Human chr14 - 64386532 64386532 64386532 TTTTCTATTTTTGGTAGAGTTGGGGTTTCACTATGTTGACCAGACTGGTCTAGATCTCAAGGGAT TTTTCTATTTTTGGTAGAGTTGGGGTTTCACTCTGTTGACCAGACTGGTCTAGATCTCAAGGGAT T G TEX21P Ensembl:ENSG00000234911 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1021639814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8250621 16517 RMVar_ID_16517 Human_SNP_ID_558317575 A-to-I Human chr14 + 64395837 64395837 64395837 GTCAGTGGTGCTGAGATCGAAAAACCCTGATCAAGAAGCTTAATGTGAGTTATTGTGTCATTGTG GTCAGTGGTGCTGAGATCGAAAAACCCTGATCGAGAAGCTTAATGTGAGTTATTGTGTCATTGTG A G MTHFD1 Ensembl:ENSG00000100714 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4902278 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_1157,GWAS_ID_1158,GWAS_ID_1159 16518 RMVar_ID_16518 Human_SNP_ID_558323042 A-to-I Human chr14 + 64418340 64418340 64418340 GATGGGGTGGGCACATGCCTGTAGTCCCAGCTACTCGGGAGGTTGAGGCAAGAGGATTGCTTGAG GATGGGGTGGGCACATGCCTGTAGTCCCAGCTCCTCGGGAGGTTGAGGCAAGAGGATTGCTTGAG A C MTHFD1 Ensembl:ENSG00000100714 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1217073907 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15478,RMVar_hsa_circ_323492,RMVar_hsa_circ_73127,RMVar_hsa_circ_72690,RMVar_hsa_circ_60114,RMVar_hsa_circ_5260,RMVar_hsa_circ_341751,RMVar_hsa_circ_347803,RMVar_hsa_circ_350322,RMVar_hsa_circ_344690,RMVar_hsa_circ_306428,RMVar_hsa_circ_73389,RMVar_hsa_circ_278312,RMVar_hsa_circ_167252,RMVar_hsa_circ_167255,RMVar_hsa_circ_302139,RMVar_hsa_circ_360780,RMVar_hsa_circ_316847,RMVar_hsa_circ_98039,RMVar_hsa_circ_299067,RMVar_hsa_circ_167256,RMVar_hsa_circ_167257,RMVar_hsa_circ_167254 16519 RMVar_ID_16519 Human_SNP_ID_558323130 A-to-I Human chr14 + 64418587 64418587 64418587 TTCTTTATTTATTTTTTTTGAGATGGAGTTTCACTCTTGTTGCCCAGGCTGGAGTGCAATGGCGC TTCTTTATTTATTTTTTTTGAGATGGAGTTTCGCTCTTGTTGCCCAGGCTGGAGTGCAATGGCGC A G MTHFD1 Ensembl:ENSG00000100714 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1348193825 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15478,RMVar_hsa_circ_323492,RMVar_hsa_circ_73127,RMVar_hsa_circ_72690,RMVar_hsa_circ_60114,RMVar_hsa_circ_5260,RMVar_hsa_circ_341751,RMVar_hsa_circ_347803,RMVar_hsa_circ_350322,RMVar_hsa_circ_344690,RMVar_hsa_circ_306428,RMVar_hsa_circ_73389,RMVar_hsa_circ_278312,RMVar_hsa_circ_167252,RMVar_hsa_circ_167255,RMVar_hsa_circ_302139,RMVar_hsa_circ_360780,RMVar_hsa_circ_316847,RMVar_hsa_circ_98039,RMVar_hsa_circ_299067,RMVar_hsa_circ_167256,RMVar_hsa_circ_167257,RMVar_hsa_circ_167254 16520 RMVar_ID_16520 Human_SNP_ID_558326831 A-to-I Human chr14 + 64432832 64432832 64432832 GCTGGAGTGCAGAGGCACAATCACAGCTCACTATAGCTTCCACCTTCCAGGTTCAAGCAATCCTC GCTGGAGTGCAGAGGCACAATCACAGCTCACTGTAGCTTCCACCTTCCAGGTTCAAGCAATCCTC A G MTHFD1 Ensembl:ENSG00000100714 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1425841309 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47694,RMVar_hsa_circ_72690,RMVar_hsa_circ_344690,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_20131,RMVar_hsa_circ_111871,RMVar_hsa_circ_368182,RMVar_hsa_circ_167260,RMVar_hsa_circ_322654,RMVar_hsa_circ_167262,RMVar_hsa_circ_358870,RMVar_hsa_circ_364297,RMVar_hsa_circ_317915,RMVar_hsa_circ_167265,RMVar_hsa_circ_352337,RMVar_hsa_circ_167263,RMVar_hsa_circ_167264,RMVar_hsa_circ_365436,RMVar_hsa_circ_75504,RMVar_hsa_circ_115797,RMVar_hsa_circ_55331,RMVar_hsa_circ_273984,RMVar_hsa_circ_297866,RMVar_hsa_circ_325031,RMVar_hsa_circ_167268,RMVar_hsa_circ_167269,RMVar_hsa_circ_167270 16521 RMVar_ID_16521 Human_SNP_ID_558326845 A-to-I Human chr14 + 64432900 64432900 64432900 TCTTAGCCTCCTGAGCACCTGGGACTATAGGTACACACACCACCACACCTGGCTAATTTTTTATT TCTTAGCCTCCTGAGCACCTGGGACTATAGGTGCACACACCACCACACCTGGCTAATTTTTTATT A G MTHFD1 Ensembl:ENSG00000100714 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs8022867 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12382289 GWAS_ID_1160,GWAS_ID_1161,GWAS_ID_1162,GWAS_ID_1163,GWAS_ID_1164,GWAS_ID_1165,GWAS_ID_1166,GWAS_ID_1167,GWAS_ID_1168,GWAS_ID_1169,GWAS_ID_1170,GWAS_ID_1171,GWAS_ID_1172,GWAS_ID_1173 RMVar_hsa_circ_47694,RMVar_hsa_circ_72690,RMVar_hsa_circ_344690,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_20131,RMVar_hsa_circ_111871,RMVar_hsa_circ_368182,RMVar_hsa_circ_167260,RMVar_hsa_circ_322654,RMVar_hsa_circ_167262,RMVar_hsa_circ_358870,RMVar_hsa_circ_364297,RMVar_hsa_circ_317915,RMVar_hsa_circ_167265,RMVar_hsa_circ_352337,RMVar_hsa_circ_167263,RMVar_hsa_circ_167264,RMVar_hsa_circ_365436,RMVar_hsa_circ_75504,RMVar_hsa_circ_115797,RMVar_hsa_circ_55331,RMVar_hsa_circ_273984,RMVar_hsa_circ_297866,RMVar_hsa_circ_325031,RMVar_hsa_circ_167268,RMVar_hsa_circ_167269,RMVar_hsa_circ_167270 16522 RMVar_ID_16522 Human_SNP_ID_558328758 A-to-I Human chr14 - 64440929 64440929 64440929 CCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCACGCCTGGCCAAAGTTGCCAGAT CCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCACGCCTGGCCAAAGTTGCCAGAT T C AL122035.1,AL122035.2 Ensembl:ENSG00000258824,Ensembl:ENSG00000272909 lincRNA,lincRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs753921022 Functional Loss SNV dbSNP153 33..33 33 - - - 16523 RMVar_ID_16523 Human_SNP_ID_558330426 A-to-I Human chr14 - 64447222 64447222 64447222 GAACCCCAGAGGCGGAGGTTGCAGTGAGTTGAAATTGCACCACTGCACTCCAGCCTGGTGACAGA GAACCCCAGAGGCGGAGGTTGCAGTGAGTTGAGATTGCACCACTGCACTCCAGCCTGGTGACAGA T C AL122035.1 Ensembl:ENSG00000258824 lincRNA intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs536537601 Functional Loss SNV dbSNP153 33..33 33 - - - 16524 RMVar_ID_16524 Human_SNP_ID_558330446 A-to-I Human chr14 - 64447294 64447294 64447294 AAAATTAACTAGGTGTGGTGGCAGGAACCTGTAGTCCCAGCTGCTTGGGAGGCTGAGGGAGGAGA AAAATTAACTAGGTGTGGTGGCAGGAACCTGTGGTCCCAGCTGCTTGGGAGGCTGAGGGAGGAGA T C AL122035.1 Ensembl:ENSG00000258824 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1252940895 Functional Loss SNV dbSNP153 33..33 33 - - - 16525 RMVar_ID_16525 Human_SNP_ID_558330945 A-to-I Human chr14 - 64449078 64449076 64449078 AAGAATTTTGCTGGCTGGGCGCGGTGGCTCACACTTGTAATCCCAACACTTTGGGAGGCCGAGGT AAGAATTTTGCTGGCTGGGCGCGGTGGCTCACGCCTGTAATCCCAACACTTTGGGAGGCCGAGGT AGT GGC - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs386778314 Functional Loss MNV dbSNP153 33..35 33 - - - 16526 RMVar_ID_16526 Human_SNP_ID_558330947 A-to-I Human chr14 - 64449078 64449078 64449078 AAGAATTTTGCTGGCTGGGCGCGGTGGCTCACACTTGTAATCCCAACACTTTGGGAGGCCGAGGT AAGAATTTTGCTGGCTGGGCGCGGTGGCTCACGCTTGTAATCCCAACACTTTGGGAGGCCGAGGT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs535013490 Functional Loss SNV dbSNP153 33..33 33 - - - 16527 RMVar_ID_16527 Human_SNP_ID_558333623 A-to-I Human chr14 + 64460864 64460864 64460864 CTTGGCCAACATGGTAAAACCCTGTTTCTACCAAAAATACAAAAATTAGCTGGGTGTGGTGGCAG CTTGGCCAACATGGTAAAACCCTGTTTCTACCCAAAATACAAAAATTAGCTGGGTGTGGTGGCAG A C MTHFD1 Ensembl:ENSG00000100714 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270170645 Functional Loss SNV dbSNP153 33..33 33 - - - 16528 RMVar_ID_16528 Human_SNP_ID_558335899 A-to-I Human chr14 + 64470332 64470332 64470332 CGCTATTTGGCCAGGGGCAGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCCAAGGCGGGT CGCTATTTGGCCAGGGGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGT A G AKAP5 Ensembl:ENSG00000179841 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1173018772 Functional Loss SNV dbSNP153 33..33 33 - - - 16529 RMVar_ID_16529 Human_SNP_ID_558336186 A-to-I Human chr14 + 64471337 64471337 64471337 ACAACGCTCGGCTAATTTTTTGTATTTTTAGTAGAGATGGGGTTTCACCGTGTTAGCCAGGATGG ACAACGCTCGGCTAATTTTTTGTATTTTTAGTGGAGATGGGGTTTCACCGTGTTAGCCAGGATGG A G AKAP5 Ensembl:ENSG00000179841 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1414314232 Functional Loss SNV dbSNP153 33..33 33 - - - 16530 RMVar_ID_16530 Human_SNP_ID_558338689 A-to-I Human chr14 - 64482259 64482259 64482259 TTTAGTAGAGATGGGGTTTCATCATGTTGGCAAGGCTGGTTTCGAACTCCTGACCTTGTGATCTG TTTAGTAGAGATGGGGTTTCATCATGTTGGCAGGGCTGGTTTCGAACTCCTGACCTTGTGATCTG T C ZBTB25 Ensembl:ENSG00000089775 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1423060183 Functional Loss SNV dbSNP153 33..33 33 - - - 16531 RMVar_ID_16531 Human_SNP_ID_558338975 A-to-I Human chr14 - 64483506 64483506 64483506 TTGGGAGGCCGAGGCGGGCGGGTCACGAGGTCAGAAGATCCAGACCATCCTGGCTAACACAGTGA TTGGGAGGCCGAGGCGGGCGGGTCACGAGGTCGGAAGATCCAGACCATCCTGGCTAACACAGTGA T C ZBTB25 Ensembl:ENSG00000089775 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1269203166 Functional Loss SNV dbSNP153 33..33 33 - - - 16532 RMVar_ID_16532 Human_SNP_ID_558338995 A-to-I Human chr14 - 64483572 64483572 64483572 CTTTGTATTTTAAAAGTTCTTCCAGCTAGGCCAGGCGTGGTGGCTCATGCTTGTAATCCCAGCAC CTTTGTATTTTAAAAGTTCTTCCAGCTAGGCCGGGCGTGGTGGCTCATGCTTGTAATCCCAGCAC T C ZBTB25 Ensembl:ENSG00000089775 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1221333477 Functional Loss SNV dbSNP153 33..33 33 - - - 16533 RMVar_ID_16533 Human_SNP_ID_558339039 A-to-I Human chr14 - 64483788 64483788 64483788 GCCCAGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGATGGTCTCGA GCCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGATGGTCTCGA T C ZBTB25 Ensembl:ENSG00000089775 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 31158229,32596459 RNA-Seq:(High) rs1428262229 Functional Loss SNV dbSNP153 33..33 33 - - - 16534 RMVar_ID_16534 Human_SNP_ID_558339041 A-to-I Human chr14 - 64483794 64483794 64483794 CACCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGATGG CACCATGCCCAGCTAATTTTTGTATTTTTAGTGGAGACAGGGTTTCACCATGTTGGCCAGGATGG T C ZBTB25 Ensembl:ENSG00000089775 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs960996157 Functional Loss SNV dbSNP153 33..33 33 - - - 16535 RMVar_ID_16535 Human_SNP_ID_558339044 A-to-I Human chr14 - 64483812 64483812 64483812 AGCCTCCTGAGCATGTGCCACCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCA AGCCTCCTGAGCATGTGCCACCATGCCCAGCTGATTTTTGTATTTTTAGTAGAGACAGGGTTTCA T C ZBTB25 Ensembl:ENSG00000089775 Protein coding intron GSE38233;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,32596459 RNA-Seq:(High) rs1465699420 Functional Loss SNV dbSNP153 33..33 33 - - - 16536 RMVar_ID_16536 Human_SNP_ID_558339056 A-to-I Human chr14 - 64483861 64483861 64483861 CAGCTCACTGCAACCTCCGCCTCTCGAATTCAAGTGATTCTCCTGCCTCAGCCTCCTGAGCATGT CAGCTCACTGCAACCTCCGCCTCTCGAATTCAGGTGATTCTCCTGCCTCAGCCTCCTGAGCATGT T C ZBTB25 Ensembl:ENSG00000089775 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1372005138 Functional Loss SNV dbSNP153 33..33 33 - - - 16537 RMVar_ID_16537 Human_SNP_ID_558339064 A-to-I Human chr14 - 64483897 64483897 64483897 GCTGTGTCGCCAGGCTGGAGTGCAGTGGTGCAATCTCAGCTCACTGCAACCTCCGCCTCTCGAAT GCTGTGTCGCCAGGCTGGAGTGCAGTGGTGCAGTCTCAGCTCACTGCAACCTCCGCCTCTCGAAT T C ZBTB25 Ensembl:ENSG00000089775 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232395894 Functional Loss SNV dbSNP153 33..33 33 - - - 16538 RMVar_ID_16538 Human_SNP_ID_558339248 A-to-I Human chr14 - 64484553 64484553 64484553 CTTAGCCTCCCAAGTAGCTTGGGATTACAGGCATGCACCACCATACCCAGCTAATTTTGTGTTTT CTTAGCCTCCCAAGTAGCTTGGGATTACAGGCGTGCACCACCATACCCAGCTAATTTTGTGTTTT T C ZBTB25 Ensembl:ENSG00000089775 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1246798512 Functional Loss SNV dbSNP153 33..33 33 - - - 16539 RMVar_ID_16539 Human_SNP_ID_558339257 A-to-I Human chr14 - 64484595 64484595 64484595 TCACTGCAATCTCTGCTGCCTGGGTTCAAGCGATTCTCCTGCCTTAGCCTCCCAAGTAGCTTGGG TCACTGCAATCTCTGCTGCCTGGGTTCAAGCGTTTCTCCTGCCTTAGCCTCCCAAGTAGCTTGGG T A ZBTB25 Ensembl:ENSG00000089775 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs562701791 Functional Loss SNV dbSNP153 33..33 33 - - - 16540 RMVar_ID_16540 Human_SNP_ID_558340423 A-to-I Human chr14 - 64489132 64489132 64489132 GCAATTCTCTTGCTTCAGTCTCCCTAGTAGCTAGGACCACAGGTGTGCGCCACCACACCCGGCTA GCAATTCTCTTGCTTCAGTCTCCCTAGTAGCTGGGACCACAGGTGTGCGCCACCACACCCGGCTA T C ZBTB25 Ensembl:ENSG00000089775 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1035926281 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120950,RMVar_hsa_circ_167292,RMVar_hsa_circ_90908,RMVar_hsa_circ_167293,RMVar_hsa_circ_167291 16541 RMVar_ID_16541 Human_SNP_ID_558340444 A-to-I Human chr14 - 64489196 64489196 64489196 GTGCCCAGGCTGAAGTGCAGTGGCATGATCTCAGCTCACTGCAACCTCCGCCTCCCAGGTTCAAG GTGCCCAGGCTGAAGTGCAGTGGCATGATCTCGGCTCACTGCAACCTCCGCCTCCCAGGTTCAAG T C ZBTB25 Ensembl:ENSG00000089775 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1478742283 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120950,RMVar_hsa_circ_167292,RMVar_hsa_circ_90908,RMVar_hsa_circ_167293,RMVar_hsa_circ_167291 16542 RMVar_ID_16542 Human_SNP_ID_558343400 A-to-I Human chr14 - 64500612 64500612 64500612 TTTTGTATTTTTAGTAGAGACGGTTTCACCATATTGGCCAGGCTGGTCTTGAACTCTGACCTCAG TTTTGTATTTTTAGTAGAGACGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCTGACCTCAG T C ZBTB25 Ensembl:ENSG00000089775 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1214264650 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79805,RMVar_hsa_circ_167292,RMVar_hsa_circ_90908,RMVar_hsa_circ_369956,RMVar_hsa_circ_167295,RMVar_hsa_circ_167294 16543 RMVar_ID_16543 Human_SNP_ID_558348317 A-to-I Human chr14 + 64519473 64519473 64519473 CTTTTTTCTTTTAACAATTAAAAAAAAAAAAAAATAGAAGAGGCCAGGTGCAGTGGCTCACACCC CTTTTTTCTTTTAACAATTAAAAAAAAAAAAATATAGAAGAGGCCAGGTGCAGTGGCTCACACCC A T ZBTB1 Ensembl:ENSG00000126804 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs77075316 Functional Loss SNV dbSNP153 33..33 33 - - - 16544 RMVar_ID_16544 Human_SNP_ID_558348400 A-to-I Human chr14 + 64519733 64519733 64519733 ATGGGAGATTGAGGCTGCAGTTAGCTATGATCATGCCACTGCACTCCAGCCTAGGTAACAGAGCG ATGGGAGATTGAGGCTGCAGTTAGCTATGATCGTGCCACTGCACTCCAGCCTAGGTAACAGAGCG A G ZBTB1 Ensembl:ENSG00000126804 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1203515352 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25107661 16545 RMVar_ID_16545 Human_SNP_ID_558348405 A-to-I Human chr14 + 64519753 64519753 64519753 TTAGCTATGATCATGCCACTGCACTCCAGCCTAGGTAACAGAGCGAGACCCTGCCTCAAAAAAAA TTAGCTATGATCATGCCACTGCACTCCAGCCTCGGTAACAGAGCGAGACCCTGCCTCAAAAAAAA A C ZBTB1 Ensembl:ENSG00000126804 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1331632929 Functional Loss SNV dbSNP153 33..33 33 - - - 16546 RMVar_ID_16546 Human_SNP_ID_558349836 A-to-I Human chr14 + 64525854 64525854 64525854 TTATTTATTTTTCTTTTTTGAGACGGAGTCTTACTCTTGCCCAGGCTGGAGTGCAGTGGTACAAT TTATTTATTTTTCTTTTTTGAGACGGAGTCTTTCTCTTGCCCAGGCTGGAGTGCAGTGGTACAAT A T ZBTB1 Ensembl:ENSG00000126804 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992820974 Functional Loss SNV dbSNP153 33..33 33 - - - 16547 RMVar_ID_16547 Human_SNP_ID_558350099 A-to-I Human chr14 + 64526918 64526916 64526918 ATTTGTTTAATTAGCAGGGCATGGTGGCATGCAGCTGTAGTCCCCAGCTACTCAGGAGGCTGAGG ATTTGTTTAATTAGCAGGGCATGGTGGCATG__GCTGTAGTCCCCAGCTACTCAGGAGGCTGAGG GCA G ZBTB1 Ensembl:ENSG00000126804 Protein coding intron GSE38233;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;Bronchiolar epithelium,BERP35T4 cell line - 24183664,31158229 RNA-Seq:(High) rs1566638029 Functional Loss DEL dbSNP153 32..33 33 - - - 16548 RMVar_ID_16548 Human_SNP_ID_558350112 A-to-I Human chr14 + 64527001 64527001 64527001 CTAGGAGTTCAAGGGAGCAGTGAGCTATGATCATGCCATTACACTCCAGCCTGGGTGACAGAGTG CTAGGAGTTCAAGGGAGCAGTGAGCTATGATCGTGCCATTACACTCCAGCCTGGGTGACAGAGTG A G ZBTB1 Ensembl:ENSG00000126804 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1489211592 Functional Loss SNV dbSNP153 33..33 33 - - - 16549 RMVar_ID_16549 Human_SNP_ID_558404043 A-to-I Human chr14 + 64748106 64748106 64748106 TGGAGAAGCTGATCAAGGGGTACCACACCTTCATGGCTCTGGCCCTGACATTTGTCCCAGTTGTG TGGAGAAGCTGATCAAGGGGTACCACACCTTCGTGGCTCTGGCCCTGACATTTGTCCCAGTTGTG A G PLEKHG3 Ensembl:ENSG00000126822 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs527315845 Functional Loss SNV dbSNP153 33..33 33 - - - 16550 RMVar_ID_16550 Human_SNP_ID_558405014 A-to-I Human chr14 + 64750574 64750574 64750574 GAGGCGGGCGGACCGCCTGAGGTCAGGAGTTCAAGACCAGCCTGGCAAACGTGGTAAAACCCCAT GAGGCGGGCGGACCGCCTGAGGTCAGGAGTTCCAGACCAGCCTGGCAAACGTGGTAAAACCCCAT A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs537046361 Functional Loss SNV dbSNP153 33..33 33 - - - 16551 RMVar_ID_16551 Human_SNP_ID_558405015 A-to-I Human chr14 + 64750574 64750574 64750574 GAGGCGGGCGGACCGCCTGAGGTCAGGAGTTCAAGACCAGCCTGGCAAACGTGGTAAAACCCCAT GAGGCGGGCGGACCGCCTGAGGTCAGGAGTTCGAGACCAGCCTGGCAAACGTGGTAAAACCCCAT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs537046361 Functional Loss SNV dbSNP153 33..33 33 - - - 16552 RMVar_ID_16552 Human_SNP_ID_558457417 A-to-I Human chr14 + 64957151 64957151 64957151 TAGAGATGAGGTCTCCCTGTATTGCCTAGACTAGTCTTGAACTCCTGGGCTCCAGCGATCCTCCC TAGAGATGAGGTCTCCCTGTATTGCCTAGACTTGTCTTGAACTCCTGGGCTCCAGCGATCCTCCC A T CHURC1-FNTB Ensembl:ENSG00000125954 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1414002522 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2456 16553 RMVar_ID_16553 Human_SNP_ID_558465703 A-to-I Human chr14 + 64989323 64989314 64989323 AAAAGTAGCTGAGCGTGGTGGCATGCACCTGTAGTCCCAGCTACTTGGGAAGCTGAGGTGGGTGA AAAAGTAGCTGAGCGTGGTGGCAT_________GTCCCAGCTACTTGGGAAGCTGAGGTGGGTGA TGCACCTGTA T CHURC1-FNTB,FNTB Ensembl:ENSG00000125954,Ensembl:ENSG00000257365 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1311173789 Functional Loss DEL dbSNP153 25..33 33 - - - RMVar_hsa_circ_2456 16554 RMVar_ID_16554 Human_SNP_ID_558474143 A-to-I Human chr14 + 65024853 65024853 65024853 GTTGCCCAGGCTGGTCTTGAACTACTGGCTTCAAGCAATCCTCCTGCCTTGGCCTCCCAAAGTAC GTTGCCCAGGCTGGTCTTGAACTACTGGCTTCGAGCAATCCTCCTGCCTTGGCCTCCCAAAGTAC A G CHURC1-FNTB,FNTB Ensembl:ENSG00000125954,Ensembl:ENSG00000257365 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1316984455 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167325,RMVar_hsa_circ_19226,RMVar_hsa_circ_321847,RMVar_hsa_circ_40631 16555 RMVar_ID_16555 Human_SNP_ID_558482113 A-to-I Human chr14 - 65057347 65057347 65057347 AGAGCTCACTGCAGCCTTGACTACCTGGGCTCAAGCGATTCTCCCACCTCAGCCTCCCAAAGTGC AGAGCTCACTGCAGCCTTGACTACCTGGGCTCCAGCGATTCTCCCACCTCAGCCTCCCAAAGTGC T G MAX Ensembl:ENSG00000125952 Protein coding intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs993114630 Functional Loss SNV dbSNP153 33..33 33 - - - 16556 RMVar_ID_16556 Human_SNP_ID_558537752 A-to-I Human chr14 + 65279293 65279293 65279293 TGTGCCATGGACGGCATTGTCCCAGATATAGCAGTTGGTACAAAGCGGGGATCTGACGAGCTTTT TGTGCCATGGACGGCATTGTCCCAGATATAGCCGTTGGTACAAAGCGGGGATCTGACGAGCTTTT A C PTBP1P Ensembl:ENSG00000259078 Pseudogene exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1346341846 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1502899,Human_RBP_ID_1822327,Human_RBP_ID_4298938,Human_RBP_ID_8407410,Human_RBP_ID_19958690,Human_RBP_ID_22798109,Human_RBP_ID_26432639,Human_RBP_ID_26926568,Human_RBP_ID_27227976 16557 RMVar_ID_16557 Human_SNP_ID_558538222 A-to-I Human chr14 + 65280968 65280968 65280968 ACCGTGCACCTCTCCAACATCCCGCCCTCAGTATCCGAGGAAGATCTCAAGGTCCTCTCCTCCAG ACCGTGCACCTCTCCAACATCCCGCCCTCAGTCTCCGAGGAAGATCTCAAGGTCCTCTCCTCCAG A C PTBP1P Ensembl:ENSG00000259078 Pseudogene exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1464626271 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5563834,Human_RBP_ID_8250474,Human_RBP_ID_26429805 16558 RMVar_ID_16558 Human_SNP_ID_558573936 A-to-I Human chr14 + 65430149 65430142 65430150 AGAATCTATCCTCCCAGCTCAGCCTCCTGAGTAGCTGGGACTGTAGACACATACCACCACGCCCA AGAATCTATCCTCCCAGCTCAGCCTC________CTGGGACTGTAGACACATACCACCACGCCCA CCTGAGTAG C FUT8 Ensembl:ENSG00000033170 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1287056798 Functional Loss DEL dbSNP153 27..34 33 - - - RMVar_hsa_circ_107530,RMVar_hsa_circ_167335 16559 RMVar_ID_16559 Human_SNP_ID_558591067 A-to-I Human chr14 + 65501199 65501199 65501199 CAGGAGTTTGAGACCAGCCTGGGTAACATAGTAAGACCTGTCTCTACAGAATTACAAACAAAAAC CAGGAGTTTGAGACCAGCCTGGGTAACATAGTGAGACCTGTCTCTACAGAATTACAAACAAAAAC A G FUT8 Ensembl:ENSG00000033170 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs925369986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6371212 RMVar_hsa_circ_37253,RMVar_hsa_circ_107530,RMVar_hsa_circ_167335,RMVar_hsa_circ_341205,RMVar_hsa_circ_329621,RMVar_hsa_circ_274254,RMVar_hsa_circ_67516,RMVar_hsa_circ_167342,RMVar_hsa_circ_167343,RMVar_hsa_circ_167346 16560 RMVar_ID_16560 Human_SNP_ID_558629210 A-to-I Human chr14 + 65654953 65654953 65654953 GATACAGAGTTTTGCAGAGACAGGGTTTCTCCATGTTGGTCAGGCTGATCTCGAACTCTGACCTC GATACAGAGTTTTGCAGAGACAGGGTTTCTCCGTGTTGGTCAGGCTGATCTCGAACTCTGACCTC A G FUT8 Ensembl:ENSG00000033170 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042783844 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37253,RMVar_hsa_circ_67516,RMVar_hsa_circ_326537,RMVar_hsa_circ_330211,RMVar_hsa_circ_167350,RMVar_hsa_circ_322053,RMVar_hsa_circ_338655,RMVar_hsa_circ_26612,RMVar_hsa_circ_39073,RMVar_hsa_circ_167352,RMVar_hsa_circ_167353,RMVar_hsa_circ_273817 16561 RMVar_ID_16561 Human_SNP_ID_558826614 A-to-I Human chr14 - 66494821 66494821 66494821 TGGGGTTTCACCATGTTAACCAGGATTGTCTCAATCTCCTGACCGCGTGATCCACCTGCCTCAGC TGGGGTTTCACCATGTTAACCAGGATTGTCTCGATCTCCTGACCGCGTGATCCACCTGCCTCAGC T C AL359232.1 Ensembl:ENSG00000258561 lincRNA intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs548518686 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1527130,Human_Splice_Rec_1527131,Human_Splice_Rec_1527138 16562 RMVar_ID_16562 Human_SNP_ID_558832626 A-to-I Human chr14 + 66518574 66518573 66518574 TACTGCAGCACTGTTCACAATAGCTAAGATATAGACTCAATCTAGGTGTCCAACAGCAGATTAAT TACTGCAGCACTGTTCACAATAGCTAAGATAT_GACTCAATCTAGGTGTCCAACAGCAGATTAAT TA T GPHN Ensembl:ENSG00000171723 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1373081727 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_18512165 16563 RMVar_ID_16563 Human_SNP_ID_558833178 A-to-I Human chr14 + 66520990 66520990 66520990 GTTTTCTGTTCCTACATTAGTTTGCTGAGGATAATGACCTCCAGCTCCATCCATGTTCCCACAAA GTTTTCTGTTCCTACATTAGTTTGCTGAGGATGATGACCTCCAGCTCCATCCATGTTCCCACAAA A G GPHN Ensembl:ENSG00000171723 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs932306081 Functional Loss SNV dbSNP153 33..33 33 - - - 16564 RMVar_ID_16564 Human_SNP_ID_558844740 A-to-I Human chr14 + 66565432 66565432 66565432 GTGATTCTCTCATCTCAGCCTCCCGAGTAGCCAGGACTACAGACATGCACCACCACACCCAGCTA GTGATTCTCTCATCTCAGCCTCCCGAGTAGCCGGGACTACAGACATGCACCACCACACCCAGCTA A G GPHN Ensembl:ENSG00000171723 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs919027377 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12387672 16565 RMVar_ID_16565 Human_SNP_ID_558886089 A-to-I Human chr14 + 66721679 66721679 66721679 ACGTTATGTAGAATTTGATTTGGGCCGGGCACAGTGCCTCATGCCTGTAATCTCAACACTTTGGA ACGTTATGTAGAATTTGATTTGGGCCGGGCACCGTGCCTCATGCCTGTAATCTCAACACTTTGGA A C GPHN Ensembl:ENSG00000171723 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs539958875 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16481,RMVar_hsa_circ_355314,RMVar_hsa_circ_358222,RMVar_hsa_circ_56576,RMVar_hsa_circ_298511,RMVar_hsa_circ_53983,RMVar_hsa_circ_48820,RMVar_hsa_circ_286640,RMVar_hsa_circ_311414,RMVar_hsa_circ_167362 16566 RMVar_ID_16566 Human_SNP_ID_558955179 A-to-I Human chr14 + 67008710 67008710 67008710 GGGACTACAAGTGCATGCCCCCATGCCCAGCTAATTTTTTGTGTTTTTAGTAGAGACAGGGTTTT GGGACTACAAGTGCATGCCCCCATGCCCAGCTCATTTTTTGTGTTTTTAGTAGAGACAGGGTTTT A C GPHN Ensembl:ENSG00000171723 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992683525 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_53983,RMVar_hsa_circ_2854,RMVar_hsa_circ_59460,RMVar_hsa_circ_69030,RMVar_hsa_circ_53815,RMVar_hsa_circ_66750,RMVar_hsa_circ_68867,RMVar_hsa_circ_13252,RMVar_hsa_circ_59106,RMVar_hsa_circ_167368,RMVar_hsa_circ_41640,RMVar_hsa_circ_68731,RMVar_hsa_circ_272229,RMVar_hsa_circ_332545,RMVar_hsa_circ_320996,RMVar_hsa_circ_277616,RMVar_hsa_circ_85417,RMVar_hsa_circ_270590,RMVar_hsa_circ_167370,RMVar_hsa_circ_167371,RMVar_hsa_circ_167369 16567 RMVar_ID_16567 Human_SNP_ID_558959540 A-to-I Human chr14 + 67027520 67027520 67027520 GCCCAGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACTATGTTGCCCAGGCTGGAACTTG GCCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACTATGTTGCCCAGGCTGGAACTTG A G GPHN Ensembl:ENSG00000171723 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1325377565 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69030,RMVar_hsa_circ_66750,RMVar_hsa_circ_13252,RMVar_hsa_circ_59106,RMVar_hsa_circ_332545,RMVar_hsa_circ_320996,RMVar_hsa_circ_277616,RMVar_hsa_circ_85417,RMVar_hsa_circ_270590,RMVar_hsa_circ_167370,RMVar_hsa_circ_167371,RMVar_hsa_circ_167369,RMVar_hsa_circ_5834,RMVar_hsa_circ_294083,RMVar_hsa_circ_326265,RMVar_hsa_circ_338005,RMVar_hsa_circ_289595,RMVar_hsa_circ_167375,RMVar_hsa_circ_167376,RMVar_hsa_circ_167374 16568 RMVar_ID_16568 Human_SNP_ID_559030262 A-to-I Human chr14 - 67323423 67323423 67323423 TTTTGTAGAGACAGGATCTCGCTTTGTTGTCCAGGCTGGTCTTGAACTCCTGGCCTCAAGCAATG TTTTGTAGAGACAGGATCTCGCTTTGTTGTCCGGGCTGGTCTTGAACTCCTGGCCTCAAGCAATG T C ATP6V1D Ensembl:ENSG00000100554 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1236892276 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_292570 16569 RMVar_ID_16569 Human_SNP_ID_559075135 A-to-I Human chr14 - 67507233 67507233 67507233 GCAATCCTCCCACTTCAGCCTCCCAAGTAGCTAGGACTGTAGTTGCACCACCTATATTAGCACCT GCAATCCTCCCACTTCAGCCTCCCAAGTAGCTGGGACTGTAGTTGCACCACCTATATTAGCACCT T C TMEM229B Ensembl:ENSG00000198133 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs983587751 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269796 16570 RMVar_ID_16570 Human_SNP_ID_559087989 A-to-I Human chr14 + 67563268 67563268 67563268 AGGGTTGAACTGTTAACTACGTGACCTTGGACATGTTACTGAACCTCTGTGCCTCAGCTTCCCTG AGGGTTGAACTGTTAACTACGTGACCTTGGACTTGTTACTGAACCTCTGTGCCTCAGCTTCCCTG A T PLEKHH1 Ensembl:ENSG00000054690 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs373614265 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9044160 RMVar_hsa_circ_269366 16571 RMVar_ID_16571 Human_SNP_ID_559088095 A-to-I Human chr14 + 67563709 67563709 67563709 CCCTCTTGGGCCTCCCAAAGTGCTGGGATTGTAAGTATGAGCCACTGAGCCTGGCTTTTTTTTTT CCCTCTTGGGCCTCCCAAAGTGCTGGGATTGTGAGTATGAGCCACTGAGCCTGGCTTTTTTTTTT A G PLEKHH1 Ensembl:ENSG00000054690 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417873962 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269366 16572 RMVar_ID_16572 Human_SNP_ID_559088298 A-to-I Human chr14 + 67564647 67564647 67564647 GCCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACTATGTTGGCCAGGCTGACATTTT GCCTGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACTATGTTGGCCAGGCTGACATTTT A G PLEKHH1 Ensembl:ENSG00000054690 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 29129909,30559470 RNA-Seq:(High) rs1039570481 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269366 16573 RMVar_ID_16573 Human_SNP_ID_559088462 A-to-I Human chr14 + 67565465 67565465 67565465 TGGAGTATCCCTATGTTGCCCAGGCTAGTCTCAAACTCCTGGCCTCAAGTGATCCTCCTTTGTCA TGGAGTATCCCTATGTTGCCCAGGCTAGTCTCCAACTCCTGGCCTCAAGTGATCCTCCTTTGTCA A C PLEKHH1 Ensembl:ENSG00000054690 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1051860205 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269366 16574 RMVar_ID_16574 Human_SNP_ID_559088485 A-to-I Human chr14 + 67565566 67565566 67565566 CTTTAAATGTAGTTCCAGCTGCTTTGAAGCCCAGCTCTCACATTCCAGCTGTACTTCCTCTTAAG CTTTAAATGTAGTTCCAGCTGCTTTGAAGCCCGGCTCTCACATTCCAGCTGTACTTCCTCTTAAG A G PLEKHH1 Ensembl:ENSG00000054690 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs997491935 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269366 16575 RMVar_ID_16575 Human_SNP_ID_559088563 A-to-I Human chr14 + 67565973 67565973 67565973 GAAACCCCATCTCTACTAAAAATACAAAAATTATTTGGGCATGGTGGTGCACGCCTATAGTCTGG GAAACCCCATCTCTACTAAAAATACAAAAATTGTTTGGGCATGGTGGTGCACGCCTATAGTCTGG A G PLEKHH1 Ensembl:ENSG00000054690 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs920550414 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269366 16576 RMVar_ID_16576 Human_SNP_ID_559088582 A-to-I Human chr14 + 67566030 67566030 67566030 TAGTCTGGCTGCTCGGGAGCCTGAGGCAGTAGAATCGCTTGAACCCAGGAGGCGAAGGTTGCAGT TAGTCTGGCTGCTCGGGAGCCTGAGGCAGTAGGATCGCTTGAACCCAGGAGGCGAAGGTTGCAGT A G PLEKHH1 Ensembl:ENSG00000054690 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935029837 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269366 16577 RMVar_ID_16577 Human_SNP_ID_559088721 A-to-I Human chr14 + 67566641 67566641 67566641 ATGGTGGCACATGCCGGTAGTCCCAGCTACTCAGGAGGCTTAAGTGGAAGTTAAGTTTGAGCCCA ATGGTGGCACATGCCGGTAGTCCCAGCTACTCGGGAGGCTTAAGTGGAAGTTAAGTTTGAGCCCA A G PLEKHH1 Ensembl:ENSG00000054690 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs944407290 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269366 16578 RMVar_ID_16578 Human_SNP_ID_559095209 A-to-I Human chr14 - 67592364 67592364 67592364 ACAATCACCACTCATTGCAGCCTCCACCTCCCAGGCTCAAGAAATCCTCCTGCCTCAGCCTCCTG ACAATCACCACTCATTGCAGCCTCCACCTCCCGGGCTCAAGAAATCCTCCTGCCTCAGCCTCCTG T C PIGH Ensembl:ENSG00000100564 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1341855584 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1528340,Human_Splice_Rec_1528341,Human_Splice_Rec_1528376,Human_Splice_Rec_1528384 16579 RMVar_ID_16579 Human_SNP_ID_559095462 A-to-I Human chr14 - 67593316 67593316 67593316 TGGCTCGTTTTTTCTATGTTTTGCAGAGATGCAGTCTCACTATGTTGCCTAGGCTGGTCTTGAAT TGGCTCGTTTTTTCTATGTTTTGCAGAGATGCGGTCTCACTATGTTGCCTAGGCTGGTCTTGAAT T C PIGH Ensembl:ENSG00000100564 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-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 16580 RMVar_ID_16580 Human_SNP_ID_559095491 A-to-I Human chr14 - 67593429 67593429 67593429 TGGAGTGCAGTGGCTCGATCACAGCTCACTGCAGCCTCAACTTCCCAGGCTCAAGCCATTCTCCC TGGAGTGCAGTGGCTCGATCACAGCTCACTGCGGCCTCAACTTCCCAGGCTCAAGCCATTCTCCC T C PIGH Ensembl:ENSG00000100564 Protein coding intron GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs375322721 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113561,RMVar_hsa_circ_345399,RMVar_hsa_circ_282693,RMVar_hsa_circ_167419 16581 RMVar_ID_16581 Human_SNP_ID_559095493 A-to-I Human chr14 - 67593444 67593434 67593445 CTCTGTTGCCCAGGCTGGAGTGCAGTGGCTCGATCACAGCTCACTGCAGCCTCAACTTCCCAGGC CTCTGTTGCCCAGGCTGGAGTGCAGTGGCTC___________ACTGCAGCCTCAACTTCCCAGGC TGAGCTGTGATC T PIGH Ensembl:ENSG00000100564 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs748094275 Functional Loss DEL dbSNP153 32..42 33 - - - RMVar_hsa_circ_113561,RMVar_hsa_circ_345399,RMVar_hsa_circ_282693,RMVar_hsa_circ_167419 16582 RMVar_ID_16582 Human_SNP_ID_559112436 A-to-I Human chr14 - 67663552 67663552 67663552 CTCCTGCCTCAGCCTCCTGAGTAGCTGGGAATACAGGCGCCCACCACCACACCAGGCTAATTTTT CTCCTGCCTCAGCCTCCTGAGTAGCTGGGAATCCAGGCGCCCACCACCACACCAGGCTAATTTTT T G VTI1B,AL049779.1 Ensembl:ENSG00000100568,Ensembl:ENSG00000258466 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1201014627 Functional Loss SNV dbSNP153 33..33 33 - - - 16583 RMVar_ID_16583 Human_SNP_ID_559114684 A-to-I Human chr14 - 67673171 67673171 67673171 TAGCTAATTATTTTTGTATTTTTAGTAGAGACAGGGTTTTGCCATGTTGGCCAGGCTGATCTCTA TAGCTAATTATTTTTGTATTTTTAGTAGAGACGGGGTTTTGCCATGTTGGCCAGGCTGATCTCTA T C VTI1B,AL049779.1 Ensembl:ENSG00000100568,Ensembl:ENSG00000258466 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs757142194 Functional Loss SNV dbSNP153 33..33 33 - - - 16584 RMVar_ID_16584 Human_SNP_ID_559114686 A-to-I Human chr14 - 67673177 67673177 67673177 CACCCCTAGCTAATTATTTTTGTATTTTTAGTAGAGACAGGGTTTTGCCATGTTGGCCAGGCTGA CACCCCTAGCTAATTATTTTTGTATTTTTAGTGGAGACAGGGTTTTGCCATGTTGGCCAGGCTGA T C VTI1B,AL049779.1 Ensembl:ENSG00000100568,Ensembl:ENSG00000258466 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs974645142 Functional Loss SNV dbSNP153 33..33 33 - - - 16585 RMVar_ID_16585 Human_SNP_ID_559116223 A-to-I Human chr14 - 67679111 67679111 67679111 CATGCCTTCCATCTTGTTATTACACAGCAAGAAGGCCTTCATCAGATGCCAGCCCCTTGATCTTG CATGCCTTCCATCTTGTTATTACACAGCAAGACGGCCTTCATCAGATGCCAGCCCCTTGATCTTG T G RDH11,AL049779.1 Ensembl:ENSG00000072042,Ensembl:ENSG00000258466 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1033593030 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17562582 RMVar_hsa_circ_167424,RMVar_hsa_circ_110732 16586 RMVar_ID_16586 Human_SNP_ID_559116227 A-to-I Human chr14 - 67679133 67679133 67679133 CCCTTCCCTCTCTTGCCCATGTCATGCCTTCCATCTTGTTATTACACAGCAAGAAGGCCTTCATC CCCTTCCCTCTCTTGCCCATGTCATGCCTTCCTTCTTGTTATTACACAGCAAGAAGGCCTTCATC T A RDH11,AL049779.1 Ensembl:ENSG00000072042,Ensembl:ENSG00000258466 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs919062210 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17562582 RMVar_hsa_circ_167424,RMVar_hsa_circ_110732 16587 RMVar_ID_16587 Human_SNP_ID_559116228 A-to-I Human chr14 - 67679133 67679133 67679133 CCCTTCCCTCTCTTGCCCATGTCATGCCTTCCATCTTGTTATTACACAGCAAGAAGGCCTTCATC CCCTTCCCTCTCTTGCCCATGTCATGCCTTCCGTCTTGTTATTACACAGCAAGAAGGCCTTCATC T C RDH11,AL049779.1 Ensembl:ENSG00000072042,Ensembl:ENSG00000258466 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs919062210 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17562582 RMVar_hsa_circ_167424,RMVar_hsa_circ_110732 16588 RMVar_ID_16588 Human_SNP_ID_559135463 A-to-I Human chr14 - 67759123 67759123 67759123 CTCCTGCCTCAGCCTCCCAAGTAGGTAGGACTACAAGCGCCCGCCACCATACCTGGCTAATTTTT CTCCTGCCTCAGCCTCCCAAGTAGGTAGGACTGCAAGCGCCCGCCACCATACCTGGCTAATTTTT T C ZFYVE26 Ensembl:ENSG00000072121 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1324826719 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44942,RMVar_hsa_circ_96741,RMVar_hsa_circ_112870,RMVar_hsa_circ_167438,RMVar_hsa_circ_167439,RMVar_hsa_circ_326430,RMVar_hsa_circ_167441,RMVar_hsa_circ_98600,RMVar_hsa_circ_114531,RMVar_hsa_circ_167442,RMVar_hsa_circ_167443,RMVar_hsa_circ_94054 16589 RMVar_ID_16589 Human_SNP_ID_559135464 A-to-I Human chr14 - 67759123 67759123 67759123 CTCCTGCCTCAGCCTCCCAAGTAGGTAGGACTACAAGCGCCCGCCACCATACCTGGCTAATTTTT CTCCTGCCTCAGCCTCCCAAGTAGGTAGGACTCCAAGCGCCCGCCACCATACCTGGCTAATTTTT T G ZFYVE26 Ensembl:ENSG00000072121 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1324826719 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44942,RMVar_hsa_circ_96741,RMVar_hsa_circ_112870,RMVar_hsa_circ_167438,RMVar_hsa_circ_167439,RMVar_hsa_circ_326430,RMVar_hsa_circ_167441,RMVar_hsa_circ_98600,RMVar_hsa_circ_114531,RMVar_hsa_circ_167442,RMVar_hsa_circ_167443,RMVar_hsa_circ_94054 16590 RMVar_ID_16590 Human_SNP_ID_559144863 A-to-I Human chr14 - 67796322 67796322 67796322 GGGTGCCCAGCTCGGGAGCCTGAGGCACGAGAATCACTTGAACCTGGGAGGCAGAGGTTGGGGTG GGGTGCCCAGCTCGGGAGCCTGAGGCACGAGAGTCACTTGAACCTGGGAGGCAGAGGTTGGGGTG T C ZFYVE26 Ensembl:ENSG00000072121 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1238946295 Functional Loss SNV dbSNP153 33..33 33 - - - 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_268243,RMVar_hsa_circ_360145,RMVar_hsa_circ_322631,RMVar_hsa_circ_267136,RMVar_hsa_circ_167455 16591 RMVar_ID_16591 Human_SNP_ID_559144879 A-to-I Human chr14 - 67796388 67796388 67796388 CAGCCTGGCTAACATAGTAAAACCCTGTCTCTACTAAAAATATGAAAGTTAGCTCGGTGTAGTGG CAGCCTGGCTAACATAGTAAAACCCTGTCTCTCCTAAAAATATGAAAGTTAGCTCGGTGTAGTGG T G ZFYVE26 Ensembl:ENSG00000072121 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs894624303 Functional Loss SNV dbSNP153 33..33 33 - - - 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_268243,RMVar_hsa_circ_360145,RMVar_hsa_circ_322631,RMVar_hsa_circ_267136,RMVar_hsa_circ_167455 16592 RMVar_ID_16592 Human_SNP_ID_559144884 A-to-I Human chr14 - 67796405 67796405 67796405 GGTAAGGAGTTCAAGACCAGCCTGGCTAACATAGTAAAACCCTGTCTCTACTAAAAATATGAAAG GGTAAGGAGTTCAAGACCAGCCTGGCTAACATGGTAAAACCCTGTCTCTACTAAAAATATGAAAG T C ZFYVE26 Ensembl:ENSG00000072121 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1566891825 Functional Loss SNV dbSNP153 33..33 33 - - - 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_268243,RMVar_hsa_circ_360145,RMVar_hsa_circ_322631,RMVar_hsa_circ_267136,RMVar_hsa_circ_167455 16593 RMVar_ID_16593 Human_SNP_ID_559144935 A-to-I Human chr14 - 67796769 67796769 67796769 GTTTGTATTTTTAGTAGAGACGGGGTTTTGCCATGTTGGCCAGGCTGATCTTGAACTCCTGACCT GTTTGTATTTTTAGTAGAGACGGGGTTTTGCCGTGTTGGCCAGGCTGATCTTGAACTCCTGACCT T C ZFYVE26 Ensembl:ENSG00000072121 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1024893437 Functional Loss SNV dbSNP153 33..33 33 - - - 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_268243,RMVar_hsa_circ_360145,RMVar_hsa_circ_322631,RMVar_hsa_circ_267136,RMVar_hsa_circ_167455 16594 RMVar_ID_16594 Human_SNP_ID_559159787 A-to-I Human chr14 + 67860031 67860031 67860031 TTTAGTAGAGACGAGGTTTCTCCATGTTGGTCAGACTGGTCTCGAACTTCCGACCTCAGGTGATC TTTAGTAGAGACGAGGTTTCTCCATGTTGGTCGGACTGGTCTCGAACTTCCGACCTCAGGTGATC A G RAD51B Ensembl:ENSG00000182185 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1427763698 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167462,RMVar_hsa_circ_167461,RMVar_hsa_circ_107080,RMVar_hsa_circ_307033,RMVar_hsa_circ_308295,RMVar_hsa_circ_167463,RMVar_hsa_circ_97609,RMVar_hsa_circ_167468 16595 RMVar_ID_16595 Human_SNP_ID_559165346 A-to-I Human chr14 + 67882979 67882979 67882979 GTTGGCCAGGCTGGTCTTGAACTCCTGACCTCAGGTGATCCGCCTGCCTTGGCCTCCCAGGGTGC GTTGGCCAGGCTGGTCTTGAACTCCTGACCTCGGGTGATCCGCCTGCCTTGGCCTCCCAGGGTGC A G RAD51B Ensembl:ENSG00000182185 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1220123807 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167462,RMVar_hsa_circ_167461,RMVar_hsa_circ_107080,RMVar_hsa_circ_307033,RMVar_hsa_circ_97609,RMVar_hsa_circ_167468,RMVar_hsa_circ_350345 16596 RMVar_ID_16596 Human_SNP_ID_559169620 A-to-I Human chr14 + 67901648 67901648 67901648 AGTAGAAGGTACCCAGAATCACAATACAGTTCACAGTAACAAAGATATGGAATCAACCAAAGTGG AGTAGAAGGTACCCAGAATCACAATACAGTTCGCAGTAACAAAGATATGGAATCAACCAAAGTGG A G RAD51B Ensembl:ENSG00000182185 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1324497077 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167461,RMVar_hsa_circ_107080,RMVar_hsa_circ_97609,RMVar_hsa_circ_167468,RMVar_hsa_circ_120057,RMVar_hsa_circ_167469 16597 RMVar_ID_16597 Human_SNP_ID_559188345 A-to-I Human chr14 + 67985835 67985835 67985835 GGGAGGCTGAGGCGGCAGGATGGCTGGAGCTCAGGAGGCGGAGGTTGTGGTGAGCTGAGGTCGTG GGGAGGCTGAGGCGGCAGGATGGCTGGAGCTCCGGAGGCGGAGGTTGTGGTGAGCTGAGGTCGTG A C RAD51B Ensembl:ENSG00000182185 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs974838583 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167461,RMVar_hsa_circ_107080,RMVar_hsa_circ_97609,RMVar_hsa_circ_167468,RMVar_hsa_circ_120057,RMVar_hsa_circ_167469 16598 RMVar_ID_16598 Human_SNP_ID_559204032 A-to-I Human chr14 + 68056587 68056587 68056587 CCTGGGCAACACGGTGAAACCCTGTCTCTACTAAAATACAAAAAATTAGCCAGGCGTGGTGATGT CCTGGGCAACACGGTGAAACCCTGTCTCTACTGAAATACAAAAAATTAGCCAGGCGTGGTGATGT A G RAD51B Ensembl:ENSG00000182185 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs563340777 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167461,RMVar_hsa_circ_107080,RMVar_hsa_circ_97609,RMVar_hsa_circ_167468,RMVar_hsa_circ_120057,RMVar_hsa_circ_167469 16599 RMVar_ID_16599 Human_SNP_ID_559209099 A-to-I Human chr14 + 68078248 68078248 68078248 GTTGTCCTGGCTGTTCTTGAACTCTGGGCCTCAAGTCATCCTTTTGCCTCAGCCTCCCAAGTAGC GTTGTCCTGGCTGTTCTTGAACTCTGGGCCTCGAGTCATCCTTTTGCCTCAGCCTCCCAAGTAGC A G RAD51B Ensembl:ENSG00000182185 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1386072504 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167461,RMVar_hsa_circ_107080,RMVar_hsa_circ_97609,RMVar_hsa_circ_167468,RMVar_hsa_circ_120057,RMVar_hsa_circ_167469 16600 RMVar_ID_16600 Human_SNP_ID_559309650 A-to-I Human chr14 + 68529336 68529336 68529336 CTCCCACATCAGCCTCCCCAGCAGCTGGGACTACAGGCGCGTGCCACCACGCCAGGCTAATTTTT CTCCCACATCAGCCTCCCCAGCAGCTGGGACTGCAGGCGCGTGCCACCACGCCAGGCTAATTTTT A G RAD51B Ensembl:ENSG00000182185 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1236509192 Functional Loss SNV dbSNP153 33..33 33 - - - 16601 RMVar_ID_16601 Human_SNP_ID_559309886 A-to-I Human chr14 + 68530351 68530351 68530351 CACCTATAGTCCCAGCTTCTTCGAGGGCTGATATGGGAGGATTGCTGGAGCCCAGAAGGTCAAGG CACCTATAGTCCCAGCTTCTTCGAGGGCTGATGTGGGAGGATTGCTGGAGCCCAGAAGGTCAAGG A G RAD51B Ensembl:ENSG00000182185 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1407787732 Functional Loss SNV dbSNP153 33..33 33 - - - 16602 RMVar_ID_16602 Human_SNP_ID_559325992 A-to-I Human chr14 + 68601523 68601522 68601523 GGAGTTCTTTGGAGAAAGGCCTTTATAAATATAAGGCATGATTAAAGGATATCAGTTTGCTAACT GGAGTTCTTTGGAGAAAGGCCTTTATAAATAT_AGGCATGATTAAAGGATATCAGTTTGCTAACT TA T RAD51B Ensembl:ENSG00000182185 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1429637546 Functional Loss DEL dbSNP153 33..33 33 - - - 16603 RMVar_ID_16603 Human_SNP_ID_559325994 A-to-I Human chr14 + 68601534 68601534 68601534 GAGAAAGGCCTTTATAAATATAAGGCATGATTAAAGGATATCAGTTTGCTAACTCTCAGAGGAAG GAGAAAGGCCTTTATAAATATAAGGCATGATTGAAGGATATCAGTTTGCTAACTCTCAGAGGAAG A G RAD51B Ensembl:ENSG00000182185 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1267044146 Functional Loss SNV dbSNP153 33..33 33 - - - 16604 RMVar_ID_16604 Human_SNP_ID_559389597 A-to-I Human chr14 - 68861850 68861850 68861850 TGCTACTGTTGGCATATCTAAGCTTTCCATCCAGCTGAAATTCGGACTCCAAAAACTCATGCCCA TGCTACTGTTGGCATATCTAAGCTTTCCATCCGGCTGAAATTCGGACTCCAAAAACTCATGCCCA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1047781410 Functional Loss SNV dbSNP153 33..33 33 - - - 16605 RMVar_ID_16605 Human_SNP_ID_559389603 A-to-I Human chr14 - 68861878 68861878 68861878 TTTCTGATCATGACGTCATTTTTGTAATTGCTACTGTTGGCATATCTAAGCTTTCCATCCAGCTG TTTCTGATCATGACGTCATTTTTGTAATTGCTGCTGTTGGCATATCTAAGCTTTCCATCCAGCTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1485723427 Functional Loss SNV dbSNP153 33..33 33 - - - 16606 RMVar_ID_16606 Human_SNP_ID_559411566 A-to-I Human chr14 - 68950111 68950111 68950111 TTTTGTATTTTCAGTAGAAACGGGGTTTCATTATGTTGGCTAGGCTGGTCTCGAACTCCTGACCT TTTTGTATTTTCAGTAGAAACGGGGTTTCATTGTGTTGGCTAGGCTGGTCTCGAACTCCTGACCT T C ACTN1 Ensembl:ENSG00000072110 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1056332909 Functional Loss SNV dbSNP153 33..33 33 - - - 16607 RMVar_ID_16607 Human_SNP_ID_559457043 A-to-I Human chr14 - 69145162 69145162 69145162 AATTTAAAAACTAGCTGGGTATGGTGGCGTGCACCTTTAGTCCCAGCTACACAGGAGGCCGAGGT AATTTAAAAACTAGCTGGGTATGGTGGCGTGCGCCTTTAGTCCCAGCTACACAGGAGGCCGAGGT T C DCAF5 Ensembl:ENSG00000139990 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs528498892 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_284410,RMVar_hsa_circ_167503 16608 RMVar_ID_16608 Human_SNP_ID_559511487 A-to-I Human chr14 - 69381099 69381099 69381099 TTTTTGTATTTTAGTAGAGACAAGGTTTCACCATGTTGGCCAGGCTAGTCTTGAACTCCTGACCT TTTTTGTATTTTAGTAGAGACAAGGTTTCACCGTGTTGGCCAGGCTAGTCTTGAACTCCTGACCT T C ERH Ensembl:ENSG00000100632 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs568780637 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98800,RMVar_hsa_circ_122006,RMVar_hsa_circ_109054,RMVar_hsa_circ_167513,RMVar_hsa_circ_167515,RMVar_hsa_circ_167514 16609 RMVar_ID_16609 Human_SNP_ID_559511500 A-to-I Human chr14 - 69381165 69381165 69381165 GCAATTCCCTTGCCTCAGCCTCCTGAGTAGGCAGGACTACAGGCGTGCACCACCATGCCCAGCTA GCAATTCCCTTGCCTCAGCCTCCTGAGTAGGCTGGACTACAGGCGTGCACCACCATGCCCAGCTA T A ERH Ensembl:ENSG00000100632 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1222182366 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98800,RMVar_hsa_circ_122006,RMVar_hsa_circ_109054,RMVar_hsa_circ_167513,RMVar_hsa_circ_167515,RMVar_hsa_circ_167514 16610 RMVar_ID_16610 Human_SNP_ID_559511507 A-to-I Human chr14 - 69381194 69381194 69381194 TCGGCTCACTGCATCCTCCACCGGTTGAAGCAATTCCCTTGCCTCAGCCTCCTGAGTAGGCAGGA TCGGCTCACTGCATCCTCCACCGGTTGAAGCAGTTCCCTTGCCTCAGCCTCCTGAGTAGGCAGGA T C ERH Ensembl:ENSG00000100632 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs143226885 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98800,RMVar_hsa_circ_122006,RMVar_hsa_circ_109054,RMVar_hsa_circ_167513,RMVar_hsa_circ_167515,RMVar_hsa_circ_167514 16611 RMVar_ID_16611 Human_SNP_ID_559522116 A-to-I Human chr14 + 69423642 69423642 69423642 CATCTCAGTCAGGCACAGTGGCTCACGCTTGTAATCTCAGCACTCTGGGAGACCGAAGCGGGCGG CATCTCAGTCAGGCACAGTGGCTCACGCTTGTCATCTCAGCACTCTGGGAGACCGAAGCGGGCGG A C SLC39A9 Ensembl:ENSG00000029364 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1045935126 Functional Loss SNV dbSNP153 33..33 33 - - - 16612 RMVar_ID_16612 Human_SNP_ID_559522117 A-to-I Human chr14 + 69423642 69423642 69423642 CATCTCAGTCAGGCACAGTGGCTCACGCTTGTAATCTCAGCACTCTGGGAGACCGAAGCGGGCGG CATCTCAGTCAGGCACAGTGGCTCACGCTTGTGATCTCAGCACTCTGGGAGACCGAAGCGGGCGG A G SLC39A9 Ensembl:ENSG00000029364 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1045935126 Functional Loss SNV dbSNP153 33..33 33 - - - 16613 RMVar_ID_16613 Human_SNP_ID_559526057 A-to-I Human chr14 + 69440465 69440465 69440465 AAAATTAGCAGGACTTGGTAGCTCACATCTGTAGTCCAGATTCTTGGGGGACTGAGGTAGGAGGA AAAATTAGCAGGACTTGGTAGCTCACATCTGTCGTCCAGATTCTTGGGGGACTGAGGTAGGAGGA A C SLC39A9 Ensembl:ENSG00000029364 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1218556855 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12399260 RMVar_hsa_circ_78832,RMVar_hsa_circ_359934,RMVar_hsa_circ_94803,RMVar_hsa_circ_167517,RMVar_hsa_circ_167518 16614 RMVar_ID_16614 Human_SNP_ID_559526071 A-to-I Human chr14 + 69440529 69440529 69440529 ATGACTTCAGTCCAGGAAATGGAGGTTACTGTAAGCTGAGATTGCACCACTGTAGTCTAGTCTGG ATGACTTCAGTCCAGGAAATGGAGGTTACTGTGAGCTGAGATTGCACCACTGTAGTCTAGTCTGG A G SLC39A9 Ensembl:ENSG00000029364 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1299000164 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12399262,Human_RBP_ID_23633390 RMVar_hsa_circ_78832,RMVar_hsa_circ_359934,RMVar_hsa_circ_94803,RMVar_hsa_circ_167517,RMVar_hsa_circ_167518 16615 RMVar_ID_16615 Human_SNP_ID_559529849 A-to-I Human chr14 + 69456381 69456381 69456381 TGCTCACTGAAAGAAGAGAAGGCTTTTCAGGTAAATGGAAAGGGTTTTTATAACACACTGTTAGC TGCTCACTGAAAGAAGAGAAGGCTTTTCAGGTGAATGGAAAGGGTTTTTATAACACACTGTTAGC A G SLC39A9 Ensembl:ENSG00000029364 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1451551050 Functional Loss SNV dbSNP153 33..33 33 - - - 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 16616 RMVar_ID_16616 Human_SNP_ID_559529870 A-to-I Human chr14 + 69456450 69456450 69456450 AAGATCAACAAACCCTTCCTTAACGGGAACTTAGCCATTCTTGGTCTCATTTTTCACGTTCCTCC AAGATCAACAAACCCTTCCTTAACGGGAACTTGGCCATTCTTGGTCTCATTTTTCACGTTCCTCC A G SLC39A9 Ensembl:ENSG00000029364 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs929972544 Functional Loss SNV dbSNP153 33..33 33 - - - 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 16617 RMVar_ID_16617 Human_SNP_ID_559530087 A-to-I Human chr14 + 69457296 69457296 69457296 GCAATCTTGGCTCACTGCAACCTCTGCCTCCCAGGTTCAGACGATTCTCCTGCCCCAGCTTCCGG GCAATCTTGGCTCACTGCAACCTCTGCCTCCCGGGTTCAGACGATTCTCCTGCCCCAGCTTCCGG A G SLC39A9 Ensembl:ENSG00000029364 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs977234114 Functional Loss SNV dbSNP153 33..33 33 - - - 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 16618 RMVar_ID_16618 Human_SNP_ID_559655607 A-to-I Human chr14 + 69979654 69979654 69979654 CAGAGCATTTTTAATTTTTATCTTTTAGAGACAAGATCTCACTATGTTGCCTAGGCTTGCCTCAA CAGAGCATTTTTAATTTTTATCTTTTAGAGACGAGATCTCACTATGTTGCCTAGGCTTGCCTCAA A G SMOC1 Ensembl:ENSG00000198732 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909887537 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6377766 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 16619 RMVar_ID_16619 Human_SNP_ID_559750300 A-to-I Human chr14 - 70362832 70362832 70362832 TTTTTGAGTGAATCAAATTAGATGGTAAGCCAAGCATGGTAGCACACACCTGTAGTCCCAGCTAC TTTTTGAGTGAATCAAATTAGATGGTAAGCCAGGCATGGTAGCACACACCTGTAGTCCCAGCTAC T C SYNJ2BP-COX16,COX16 Ensembl:ENSG00000258644,Ensembl:ENSG00000133983 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1283791169 Functional Loss SNV dbSNP153 33..33 33 - - - 16620 RMVar_ID_16620 Human_SNP_ID_559751180 A-to-I Human chr14 - 70367382 70367382 70367382 AATTTTTGTATTTTTAGTAGACACGGGGTTTCAGCATCTTGGCCAGGCTGGTCTTGAATTCCTGA AATTTTTGTATTTTTAGTAGACACGGGGTTTCGGCATCTTGGCCAGGCTGGTCTTGAATTCCTGA T C SYNJ2BP,SYNJ2BP-COX16,COX16 Ensembl:ENSG00000213463,Ensembl:ENSG00000258644,Ensembl:ENSG00000133983 Protein coding,Protein coding,Protein coding 3'UTR,intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs972396263 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_450899,Human_RBP_ID_999268,Human_RBP_ID_6378324,Human_RBP_ID_8795785 RMVar_hsa_circ_167562,RMVar_hsa_circ_88506 16621 RMVar_ID_16621 Human_SNP_ID_559751209 A-to-I Human chr14 - 70367505 70367505 70367505 TAGGCTGGAGTGCAGTGGCACGATCTCAGCTCACTGCAATCTCTGCCGCCCGGGTTCAAGCGATT TAGGCTGGAGTGCAGTGGCACGATCTCAGCTCGCTGCAATCTCTGCCGCCCGGGTTCAAGCGATT T C SYNJ2BP,SYNJ2BP-COX16,COX16 Ensembl:ENSG00000213463,Ensembl:ENSG00000258644,Ensembl:ENSG00000133983 Protein coding,Protein coding,Protein coding 3'UTR,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1420864524 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167562,RMVar_hsa_circ_88506 16622 RMVar_ID_16622 Human_SNP_ID_559751645 A-to-I Human chr14 - 70369354 70369354 70369354 ATGGTGGCTCATGCCTGTAATCCCAGCACTCTAGGAGGCCTAGGCAGGTGGGTCACTTGAGCTCA ATGGTGGCTCATGCCTGTAATCCCAGCACTCTGGGAGGCCTAGGCAGGTGGGTCACTTGAGCTCA T C SYNJ2BP,SYNJ2BP-COX16,COX16 Ensembl:ENSG00000213463,Ensembl:ENSG00000258644,Ensembl:ENSG00000133983 Protein coding,Protein coding,Protein coding 3'UTR,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1138079 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6378365 RMVar_hsa_circ_167562,RMVar_hsa_circ_88506 16623 RMVar_ID_16623 Human_SNP_ID_559752080 A-to-I Human chr14 - 70371481 70371481 70371481 CAGGACCTGGGAGACGGAGGTTGCAGTGAGCCAAGATCACGCCACTGCACTCCAGCCTGGGCTAC CAGGACCTGGGAGACGGAGGTTGCAGTGAGCCTAGATCACGCCACTGCACTCCAGCCTGGGCTAC T A SYNJ2BP,SYNJ2BP-COX16,COX16 Ensembl:ENSG00000213463,Ensembl:ENSG00000258644,Ensembl:ENSG00000133983 Protein coding,Protein coding,Protein coding 3'UTR,intron,intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs916006538 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6378409,Human_RBP_ID_12403950 RMVar_hsa_circ_167562,RMVar_hsa_circ_88506 16624 RMVar_ID_16624 Human_SNP_ID_559752093 A-to-I Human chr14 - 70371543 70371543 70371543 ATGGTGGCGCGTTCCTGTAATTCCAGCTACTCAGGAGGCTGAGGCAGGAGAACTGTTTGAACCAG ATGGTGGCGCGTTCCTGTAATTCCAGCTACTCGGGAGGCTGAGGCAGGAGAACTGTTTGAACCAG T C SYNJ2BP,SYNJ2BP-COX16,COX16 Ensembl:ENSG00000213463,Ensembl:ENSG00000258644,Ensembl:ENSG00000133983 Protein coding,Protein coding,Protein coding 3'UTR,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs887339692 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6378411 RMVar_hsa_circ_167562,RMVar_hsa_circ_88506 16625 RMVar_ID_16625 Human_SNP_ID_559752094 A-to-I Human chr14 - 70371547 70371547 70371547 GGACATGGTGGCGCGTTCCTGTAATTCCAGCTACTCAGGAGGCTGAGGCAGGAGAACTGTTTGAA GGACATGGTGGCGCGTTCCTGTAATTCCAGCTGCTCAGGAGGCTGAGGCAGGAGAACTGTTTGAA T C SYNJ2BP,SYNJ2BP-COX16,COX16 Ensembl:ENSG00000213463,Ensembl:ENSG00000258644,Ensembl:ENSG00000133983 Protein coding,Protein coding,Protein coding 3'UTR,intron,intron GSE38233;GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1315481562 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6378411 RMVar_hsa_circ_167562,RMVar_hsa_circ_88506 16626 RMVar_ID_16626 Human_SNP_ID_559803638 A-to-I Human chr14 - 70584657 70584657 70584657 TTGAAAGGATATTAGGCCGGATGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCATG TTGAAAGGATATTAGGCCGGATGTGGTGGCTCGCGCCTGTAATCCCAGCACTTTGGGAGGCCATG T C MED6 Ensembl:ENSG00000133997 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982976272 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22577570 Human_miRNA_ID_1942959,Human_miRNA_ID_2117150,Human_miRNA_ID_2200729,Human_miRNA_ID_2203792,Human_miRNA_ID_2316267,Human_miRNA_ID_2319422,Human_miRNA_ID_2325751,Human_miRNA_ID_2520129,Human_miRNA_ID_2523291,Human_miRNA_ID_2775132,Human_miRNA_ID_2822489,Human_miRNA_ID_2835892,Human_miRNA_ID_3113245 RMVar_hsa_circ_92766,RMVar_hsa_circ_167568,RMVar_hsa_circ_75899,RMVar_hsa_circ_167567 16627 RMVar_ID_16627 Human_SNP_ID_559854899 A-to-I Human chr14 - 70798643 70798643 70798643 AAACCCCGTCTCTACTAAAAATACAAAAAATTAGCCGGGCGTAGTGGCGGGTGCCTGTAGTCCCA AAACCCCGTCTCTACTAAAAATACAAAAAATTTGCCGGGCGTAGTGGCGGGTGCCTGTAGTCCCA T A MAP3K9 Ensembl:ENSG00000006432 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1439361402 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_120880 RMVar_hsa_circ_41225,RMVar_hsa_circ_360017 16628 RMVar_ID_16628 Human_SNP_ID_559858344 A-to-I Human chr14 + 70811782 70811782 70811782 TGTTTGAGAGGCTGAGGCAGGAAGATTGCTTGAACCTAGGAGGTCAAGGCTGTAGTGAACAGTGT TGTTTGAGAGGCTGAGGCAGGAAGATTGCTTGCACCTAGGAGGTCAAGGCTGTAGTGAACAGTGT A C AC004816.1 Ensembl:ENSG00000259153 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1394863913 Functional Loss SNV dbSNP153 33..33 33 - - - 16629 RMVar_ID_16629 Human_SNP_ID_559886966 A-to-I Human chr14 + 70925241 70925241 70925241 GGACTCCGGACCTCAAGTGATCTGCCTGCTTCAGCCTCCCAAAGTGCTGGGATTACAAGCATGAG GGACTCCGGACCTCAAGTGATCTGCCTGCTTCGGCCTCCCAAAGTGCTGGGATTACAAGCATGAG A G PCNX1 Ensembl:ENSG00000100731 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1008747082 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85442,RMVar_hsa_circ_167585 16630 RMVar_ID_16630 Human_SNP_ID_559886968 A-to-I Human chr14 + 70925250 70925250 70925250 ACCTCAAGTGATCTGCCTGCTTCAGCCTCCCAAAGTGCTGGGATTACAAGCATGAGCCACGAAGC ACCTCAAGTGATCTGCCTGCTTCAGCCTCCCAGAGTGCTGGGATTACAAGCATGAGCCACGAAGC A G PCNX1 Ensembl:ENSG00000100731 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1471677277 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8409163 RMVar_hsa_circ_85442,RMVar_hsa_circ_167585 16631 RMVar_ID_16631 Human_SNP_ID_559904636 A-to-I Human chr14 + 70989677 70989677 70989677 TCAGCCTCCCGAGGAGCTGGGATTACAGGTGCATACCACCCTGCCTGGCTAATTTTTATATTATT TCAGCCTCCCGAGGAGCTGGGATTACAGGTGCCTACCACCCTGCCTGGCTAATTTTTATATTATT A C PCNX1 Ensembl:ENSG00000100731 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1172444836 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69303,RMVar_hsa_circ_85442,RMVar_hsa_circ_312286,RMVar_hsa_circ_356179,RMVar_hsa_circ_167585,RMVar_hsa_circ_120823,RMVar_hsa_circ_99201,RMVar_hsa_circ_127516,RMVar_hsa_circ_167587,RMVar_hsa_circ_167586,RMVar_hsa_circ_320723,RMVar_hsa_circ_311868,RMVar_hsa_circ_69410,RMVar_hsa_circ_105320,RMVar_hsa_circ_20475,RMVar_hsa_circ_40454,RMVar_hsa_circ_101126,RMVar_hsa_circ_167595,RMVar_hsa_circ_167597,RMVar_hsa_circ_167596,RMVar_hsa_circ_267774,RMVar_hsa_circ_345618,RMVar_hsa_circ_167594,RMVar_hsa_circ_332604,RMVar_hsa_circ_344620,RMVar_hsa_circ_374191,RMVar_hsa_circ_167601,RMVar_hsa_circ_374051,RMVar_hsa_circ_333438,RMVar_hsa_circ_265992,RMVar_hsa_circ_298227,RMVar_hsa_circ_308016,RMVar_hsa_circ_280868,RMVar_hsa_circ_90324,RMVar_hsa_circ_122581,RMVar_hsa_circ_80164,RMVar_hsa_circ_288688,RMVar_hsa_circ_167604,RMVar_hsa_circ_167606,RMVar_hsa_circ_167608,RMVar_hsa_circ_167610,RMVar_hsa_circ_167609,RMVar_hsa_circ_167607,RMVar_hsa_circ_167605,RMVar_hsa_circ_334030,RMVar_hsa_circ_167602,RMVar_hsa_circ_167603,RMVar_hsa_circ_369748,RMVar_hsa_circ_373820,RMVar_hsa_circ_369559,RMVar_hsa_circ_338205,RMVar_hsa_circ_307092,RMVar_hsa_circ_314316,RMVar_hsa_circ_301472,RMVar_hsa_circ_103013,RMVar_hsa_circ_268871,RMVar_hsa_circ_279501,RMVar_hsa_circ_127817,RMVar_hsa_circ_85251,RMVar_hsa_circ_99852,RMVar_hsa_circ_52867,RMVar_hsa_circ_167614,RMVar_hsa_circ_167618,RMVar_hsa_circ_167620,RMVar_hsa_circ_167621,RMVar_hsa_circ_167619,RMVar_hsa_circ_167616,RMVar_hsa_circ_167617,RMVar_hsa_circ_167615,RMVar_hsa_circ_167623,RMVar_hsa_circ_167612,RMVar_hsa_circ_167613,RMVar_hsa_circ_167624,RMVar_hsa_circ_378329 16632 RMVar_ID_16632 Human_SNP_ID_559904643 A-to-I Human chr14 + 70989718 70989718 70989718 TGCCTGGCTAATTTTTATATTATTGTAGAGACAGGGTTTTTTTGCCTTGTTGGCCAGGCTGGTCT TGCCTGGCTAATTTTTATATTATTGTAGAGACGGGGTTTTTTTGCCTTGTTGGCCAGGCTGGTCT A G PCNX1 Ensembl:ENSG00000100731 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs940211690 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69303,RMVar_hsa_circ_85442,RMVar_hsa_circ_312286,RMVar_hsa_circ_356179,RMVar_hsa_circ_167585,RMVar_hsa_circ_120823,RMVar_hsa_circ_99201,RMVar_hsa_circ_127516,RMVar_hsa_circ_167587,RMVar_hsa_circ_167586,RMVar_hsa_circ_320723,RMVar_hsa_circ_311868,RMVar_hsa_circ_69410,RMVar_hsa_circ_105320,RMVar_hsa_circ_20475,RMVar_hsa_circ_40454,RMVar_hsa_circ_101126,RMVar_hsa_circ_167595,RMVar_hsa_circ_167597,RMVar_hsa_circ_167596,RMVar_hsa_circ_267774,RMVar_hsa_circ_345618,RMVar_hsa_circ_167594,RMVar_hsa_circ_332604,RMVar_hsa_circ_344620,RMVar_hsa_circ_374191,RMVar_hsa_circ_167601,RMVar_hsa_circ_374051,RMVar_hsa_circ_333438,RMVar_hsa_circ_265992,RMVar_hsa_circ_298227,RMVar_hsa_circ_308016,RMVar_hsa_circ_280868,RMVar_hsa_circ_90324,RMVar_hsa_circ_122581,RMVar_hsa_circ_80164,RMVar_hsa_circ_288688,RMVar_hsa_circ_167604,RMVar_hsa_circ_167606,RMVar_hsa_circ_167608,RMVar_hsa_circ_167610,RMVar_hsa_circ_167609,RMVar_hsa_circ_167607,RMVar_hsa_circ_167605,RMVar_hsa_circ_334030,RMVar_hsa_circ_167602,RMVar_hsa_circ_167603,RMVar_hsa_circ_369748,RMVar_hsa_circ_373820,RMVar_hsa_circ_369559,RMVar_hsa_circ_338205,RMVar_hsa_circ_307092,RMVar_hsa_circ_314316,RMVar_hsa_circ_301472,RMVar_hsa_circ_103013,RMVar_hsa_circ_268871,RMVar_hsa_circ_279501,RMVar_hsa_circ_127817,RMVar_hsa_circ_85251,RMVar_hsa_circ_99852,RMVar_hsa_circ_52867,RMVar_hsa_circ_167614,RMVar_hsa_circ_167618,RMVar_hsa_circ_167620,RMVar_hsa_circ_167621,RMVar_hsa_circ_167619,RMVar_hsa_circ_167616,RMVar_hsa_circ_167617,RMVar_hsa_circ_167615,RMVar_hsa_circ_167623,RMVar_hsa_circ_167612,RMVar_hsa_circ_167613,RMVar_hsa_circ_167624,RMVar_hsa_circ_378329 16633 RMVar_ID_16633 Human_SNP_ID_559936383 A-to-I Human chr14 + 71115335 71115335 71115335 TTTTGGCAAATATATTGCATCAAAAATACAGTATTGACAGTGGATAAAACACTGAGGAAATAAAT TTTTGGCAAATATATTGCATCAAAAATACAGTGTTGACAGTGGATAAAACACTGAGGAAATAAAT A G PCNX1 Ensembl:ENSG00000100731 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs763633431 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_451178,Human_RBP_ID_1498573,Human_RBP_ID_3460106 Human_miRNA_ID_530939,Human_miRNA_ID_537126,Human_miRNA_ID_1253649,Human_miRNA_ID_2188223,Human_miRNA_ID_2190592,Human_miRNA_ID_2605356,Human_miRNA_ID_2969123 RMVar_hsa_circ_120823,RMVar_hsa_circ_167586,RMVar_hsa_circ_109704,RMVar_hsa_circ_167677,RMVar_hsa_circ_264913,RMVar_hsa_circ_106006,RMVar_hsa_circ_167687 16634 RMVar_ID_16634 Human_SNP_ID_559982131 A-to-I Human chr14 - 71310582 71310582 71310582 CCTCCCGGTTTCAAGTGAATTCTCCAGCCTCAACTTCACAAGTAGCTGGGATTACAGGTGCGCAC CCTCCCGGTTTCAAGTGAATTCTCCAGCCTCAGCTTCACAAGTAGCTGGGATTACAGGTGCGCAC T C AC005476.2 Ensembl:ENSG00000259146 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1010264866 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1531228,Human_Splice_Rec_1531229 16635 RMVar_ID_16635 Human_SNP_ID_559987293 A-to-I Human chr14 - 71330595 71330595 71330595 GCCCCAAACCATCACACTGAAGAAGCCTCCTGAAGCTCAGTTGGGATTTAACATCTGAGGAGGAA GCCCCAAACCATCACACTGAAGAAGCCTCCTGGAGCTCAGTTGGGATTTAACATCTGAGGAGGAA T C AC005476.1 Ensembl:ENSG00000259079 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878905179 Functional Loss SNV dbSNP153 33..33 33 - - - 16636 RMVar_ID_16636 Human_SNP_ID_559988914 A-to-I Human chr14 + 71337839 71337839 71337839 ATGGTGATGCATGCCTGTAGTCCCAGCTGTTCAGGAGGCTGAGATGGGAGGATCGCATGAGGCCA ATGGTGATGCATGCCTGTAGTCCCAGCTGTTCCGGAGGCTGAGATGGGAGGATCGCATGAGGCCA A C SIPA1L1 Ensembl:ENSG00000197555 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444988315 Functional Loss SNV dbSNP153 33..33 33 - - - 16637 RMVar_ID_16637 Human_SNP_ID_559996927 A-to-I Human chr14 + 71371457 71371457 71371457 TCACCTAGGCTGGAGTGCAGTGGTGTGATCTCAGCTCACTGCATCCTCGACCTCCCTGGCTCAAG TCACCTAGGCTGGAGTGCAGTGGTGTGATCTCGGCTCACTGCATCCTCGACCTCCCTGGCTCAAG A G SIPA1L1 Ensembl:ENSG00000197555 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs927929031 Functional Loss SNV dbSNP153 33..33 33 - - - 16638 RMVar_ID_16638 Human_SNP_ID_560002822 A-to-I Human chr14 + 71395542 71395542 71395542 ACAATTAGCTGGGCGCAGTAGGACTTGCCTGTAGTCCCAGCTACTGGGGGCTGAGGTGCGAGGAT ACAATTAGCTGGGCGCAGTAGGACTTGCCTGTGGTCCCAGCTACTGGGGGCTGAGGTGCGAGGAT A G SIPA1L1 Ensembl:ENSG00000197555 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1449961243 Functional Loss SNV dbSNP153 33..33 33 - - - 16639 RMVar_ID_16639 Human_SNP_ID_560005666 A-to-I Human chr14 + 71407694 71407694 71407694 ACACCTGCCTAATTTATGTTTTTTGTAGAGACAAGGTTTTGCCATGTTGTCCAGGCTGGTGAATT ACACCTGCCTAATTTATGTTTTTTGTAGAGACGAGGTTTTGCCATGTTGTCCAGGCTGGTGAATT A G SIPA1L1 Ensembl:ENSG00000197555 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1416903905 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167689,RMVar_hsa_circ_298425,RMVar_hsa_circ_326686,RMVar_hsa_circ_273797 16640 RMVar_ID_16640 Human_SNP_ID_560011602 A-to-I Human chr14 + 71432123 71432123 71432123 TGAGAAAGGATCTTGTCTCTGTAGCCCAGGCTAGAGTACATTGGCGTGATCACAGCTCACTGCAG TGAGAAAGGATCTTGTCTCTGTAGCCCAGGCTGGAGTACATTGGCGTGATCACAGCTCACTGCAG A G SIPA1L1 Ensembl:ENSG00000197555 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs998280407 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167691,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_120951,RMVar_hsa_circ_271774,RMVar_hsa_circ_113472,RMVar_hsa_circ_167692,RMVar_hsa_circ_66822,RMVar_hsa_circ_336122,RMVar_hsa_circ_315837 16641 RMVar_ID_16641 Human_SNP_ID_560011635 A-to-I Human chr14 + 71432274 71432274 71432274 TTTTTTATTTTTTGTAGAGATGAGGCCTTACTATGTTGCCAGGTTGGTCTTGAACTCCTGGGCTC TTTTTTATTTTTTGTAGAGATGAGGCCTTACTGTGTTGCCAGGTTGGTCTTGAACTCCTGGGCTC A G SIPA1L1 Ensembl:ENSG00000197555 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs369380017 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167691,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_120951,RMVar_hsa_circ_271774,RMVar_hsa_circ_113472,RMVar_hsa_circ_167692,RMVar_hsa_circ_66822,RMVar_hsa_circ_336122,RMVar_hsa_circ_315837 16642 RMVar_ID_16642 Human_SNP_ID_560013509 A-to-I Human chr14 + 71440210 71440210 71440210 ACCATTCCTGGCTGATTTTTTTCTATTTTAGTAGAGATGGGGTTTCACCATGTTGCCCAGGCTGG ACCATTCCTGGCTGATTTTTTTCTATTTTAGTGGAGATGGGGTTTCACCATGTTGCCCAGGCTGG A G SIPA1L1 Ensembl:ENSG00000197555 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1001021720 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167691,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_120951,RMVar_hsa_circ_271774,RMVar_hsa_circ_113472,RMVar_hsa_circ_167692,RMVar_hsa_circ_66822,RMVar_hsa_circ_336122,RMVar_hsa_circ_315837 16643 RMVar_ID_16643 Human_SNP_ID_560014879 A-to-I Human chr14 + 71446031 71446031 71446031 CCACCATGCCCAACTAATTTTGTTATTTTTGTAGAAGATGGAATCTCACTGTGTTGCCCAGGCTG CCACCATGCCCAACTAATTTTGTTATTTTTGTGGAAGATGGAATCTCACTGTGTTGCCCAGGCTG A G SIPA1L1 Ensembl:ENSG00000197555 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1324142861 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12410290 RMVar_hsa_circ_167691,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_120951,RMVar_hsa_circ_271774,RMVar_hsa_circ_113472,RMVar_hsa_circ_167692,RMVar_hsa_circ_66822,RMVar_hsa_circ_336122,RMVar_hsa_circ_315837 16644 RMVar_ID_16644 Human_SNP_ID_560014892 A-to-I Human chr14 + 71446096 71446096 71446096 ATCTTGGACTTCTGGGCTAAAGTGATCCTCCCACTTTGGCCTCATAAAGTATTGGGATTACAGGC ATCTTGGACTTCTGGGCTAAAGTGATCCTCCCGCTTTGGCCTCATAAAGTATTGGGATTACAGGC A G SIPA1L1 Ensembl:ENSG00000197555 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs751940616 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167691,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_120951,RMVar_hsa_circ_271774,RMVar_hsa_circ_113472,RMVar_hsa_circ_167692,RMVar_hsa_circ_66822,RMVar_hsa_circ_336122,RMVar_hsa_circ_315837 16645 RMVar_ID_16645 Human_SNP_ID_560021123 A-to-I Human chr14 + 71471193 71471193 71471193 AGTGTTTTCCACTTAATAGTGGGAATTGGGCCAGGTGCATTGGCTCATGCCTGTAATCCCAGGAC AGTGTTTTCCACTTAATAGTGGGAATTGGGCCGGGTGCATTGGCTCATGCCTGTAATCCCAGGAC A G SIPA1L1 Ensembl:ENSG00000197555 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1012365794 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2750885,Human_miRNA_ID_2753688,Human_miRNA_ID_2755624 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_113472,RMVar_hsa_circ_167692,RMVar_hsa_circ_66822,RMVar_hsa_circ_336122,RMVar_hsa_circ_315837,RMVar_hsa_circ_167693 16646 RMVar_ID_16646 Human_SNP_ID_560021197 A-to-I Human chr14 + 71471451 71471451 71471451 AGATTGTACCACTGCACTCCAGCCTGGGCAACAAAGCAAGACTCTGTCTTGGGGGAAAAAAGTGT AGATTGTACCACTGCACTCCAGCCTGGGCAACCAAGCAAGACTCTGTCTTGGGGGAAAAAAGTGT A C SIPA1L1 Ensembl:ENSG00000197555 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs999577982 Functional Loss SNV dbSNP153 33..33 33 - - - 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_113472,RMVar_hsa_circ_167692,RMVar_hsa_circ_66822,RMVar_hsa_circ_336122,RMVar_hsa_circ_315837,RMVar_hsa_circ_167693 16647 RMVar_ID_16647 Human_SNP_ID_560023458 A-to-I Human chr14 + 71480506 71480506 71480506 GAAGTCAGCCGTGCACAGTGGCTCACGCCTGTAATCCCAGCATTTTGGGAGGCCTAGTTGGGTGG GAAGTCAGCCGTGCACAGTGGCTCACGCCTGTTATCCCAGCATTTTGGGAGGCCTAGTTGGGTGG A T SIPA1L1 Ensembl:ENSG00000197555 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910962894 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2086645 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_113472,RMVar_hsa_circ_167692,RMVar_hsa_circ_66822,RMVar_hsa_circ_336122,RMVar_hsa_circ_315837,RMVar_hsa_circ_167693 16648 RMVar_ID_16648 Human_SNP_ID_560027473 A-to-I Human chr14 + 71497273 71497273 71497273 TGCTATATTGCCCAGGCTGGTCTTGAACTCCTAGACTCAAGGGATCGTTCTTCCTTGGCCTCCCA TGCTATATTGCCCAGGCTGGTCTTGAACTCCTGGACTCAAGGGATCGTTCTTCCTTGGCCTCCCA A G SIPA1L1 Ensembl:ENSG00000197555 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1389406256 Functional Loss SNV dbSNP153 33..33 33 - - - 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 16649 RMVar_ID_16649 Human_SNP_ID_560031975 A-to-I Human chr14 + 71515777 71515777 71515777 CTCCTGTCTCAGCCTCCCAAATAACTGCTACTACACGCACATGCCACCAGGCCCAGCTAATTTTT CTCCTGTCTCAGCCTCCCAAATAACTGCTACTGCACGCACATGCCACCAGGCCCAGCTAATTTTT A G SIPA1L1 Ensembl:ENSG00000197555 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005228541 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_326686,RMVar_hsa_circ_303569,RMVar_hsa_circ_336115,RMVar_hsa_circ_342753,RMVar_hsa_circ_304615,RMVar_hsa_circ_271774,RMVar_hsa_circ_79264,RMVar_hsa_circ_66822,RMVar_hsa_circ_315837,RMVar_hsa_circ_167693,RMVar_hsa_circ_297076,RMVar_hsa_circ_363542,RMVar_hsa_circ_167694,RMVar_hsa_circ_335518,RMVar_hsa_circ_167696 16650 RMVar_ID_16650 Human_SNP_ID_560047451 A-to-I Human chr14 + 71578050 71578050 71578050 CTCCTACCTCAGCCTCCCAAGTACCTCGGATTACAGGCACACGCTATCATGCCTGGCTAATTTTT CTCCTACCTCAGCCTCCCAAGTACCTCGGATTGCAGGCACACGCTATCATGCCTGGCTAATTTTT A G SIPA1L1 Ensembl:ENSG00000197555 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1331053595 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_336115,RMVar_hsa_circ_342753,RMVar_hsa_circ_304615,RMVar_hsa_circ_66822,RMVar_hsa_circ_363542,RMVar_hsa_circ_335518,RMVar_hsa_circ_167697,RMVar_hsa_circ_61785,RMVar_hsa_circ_370002 16651 RMVar_ID_16651 Human_SNP_ID_560075126 A-to-I Human chr14 + 71691334 71691334 71691334 CCTGTGTTGGCTGGGTGCTGTGGTTTATGCCTATAATCCCACCACTTTGGGAGGCCAAGGCTGGT CCTGTGTTGGCTGGGTGCTGTGGTTTATGCCTCTAATCCCACCACTTTGGGAGGCCAAGGCTGGT A C SIPA1L1 Ensembl:ENSG00000197555 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs979912370 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32388,RMVar_hsa_circ_14553,RMVar_hsa_circ_65963,RMVar_hsa_circ_109725,RMVar_hsa_circ_378567,RMVar_hsa_circ_167707,RMVar_hsa_circ_295576,RMVar_hsa_circ_36153,RMVar_hsa_circ_369796,RMVar_hsa_circ_314556,RMVar_hsa_circ_167711,RMVar_hsa_circ_167712 16652 RMVar_ID_16652 Human_SNP_ID_560075127 A-to-I Human chr14 + 71691334 71691334 71691334 CCTGTGTTGGCTGGGTGCTGTGGTTTATGCCTATAATCCCACCACTTTGGGAGGCCAAGGCTGGT CCTGTGTTGGCTGGGTGCTGTGGTTTATGCCTGTAATCCCACCACTTTGGGAGGCCAAGGCTGGT A G SIPA1L1 Ensembl:ENSG00000197555 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs979912370 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32388,RMVar_hsa_circ_14553,RMVar_hsa_circ_65963,RMVar_hsa_circ_109725,RMVar_hsa_circ_378567,RMVar_hsa_circ_167707,RMVar_hsa_circ_295576,RMVar_hsa_circ_36153,RMVar_hsa_circ_369796,RMVar_hsa_circ_314556,RMVar_hsa_circ_167711,RMVar_hsa_circ_167712 16653 RMVar_ID_16653 Human_SNP_ID_560075128 A-to-I Human chr14 + 71691336 71691336 71691336 TGTGTTGGCTGGGTGCTGTGGTTTATGCCTATAATCCCACCACTTTGGGAGGCCAAGGCTGGTGC TGTGTTGGCTGGGTGCTGTGGTTTATGCCTATCATCCCACCACTTTGGGAGGCCAAGGCTGGTGC A C SIPA1L1 Ensembl:ENSG00000197555 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs576017529 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32388,RMVar_hsa_circ_14553,RMVar_hsa_circ_65963,RMVar_hsa_circ_109725,RMVar_hsa_circ_378567,RMVar_hsa_circ_167707,RMVar_hsa_circ_295576,RMVar_hsa_circ_36153,RMVar_hsa_circ_369796,RMVar_hsa_circ_314556,RMVar_hsa_circ_167711,RMVar_hsa_circ_167712 16654 RMVar_ID_16654 Human_SNP_ID_560077489 A-to-I Human chr14 + 71700831 71700831 71700831 CCTGGCTAACATGGTGAAACCTCTTCTCTACTAAAAATACAAAAAATTAGCTGGGTGTGGTGGCG CCTGGCTAACATGGTGAAACCTCTTCTCTACTGAAAATACAAAAAATTAGCTGGGTGTGGTGGCG A G SIPA1L1 Ensembl:ENSG00000197555 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1161621468 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32388,RMVar_hsa_circ_14553,RMVar_hsa_circ_65963,RMVar_hsa_circ_109725,RMVar_hsa_circ_378567,RMVar_hsa_circ_167707,RMVar_hsa_circ_295576,RMVar_hsa_circ_369796,RMVar_hsa_circ_314556,RMVar_hsa_circ_167711,RMVar_hsa_circ_167712,RMVar_hsa_circ_167713,RMVar_hsa_circ_285900,RMVar_hsa_circ_359812 16655 RMVar_ID_16655 Human_SNP_ID_560323693 A-to-I Human chr14 - 72670635 72670635 72670635 TTTTTTGCGAGAGAGAGAGAGAGAGAGAGAGAAGGGAAATCAAAGAAATCGAAGCAATATCCTGT TTTTTTGCGAGAGAGAGAGAGAGAGAGAGAGAGGGGAAATCAAAGAAATCGAAGCAATATCCTGT T C DPF3 Ensembl:ENSG00000205683 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs200358708 Functional Loss SNV dbSNP153 33..33 33 - - - 16656 RMVar_ID_16656 Human_SNP_ID_560404708 A-to-I Human chr14 - 72997869 72997869 72997869 GCTCGCTGTGGCCTGGATGTCCCTTTATCCACACTGGGCCCTGCAGTTATCATCTTCCATGAGAC GCTCGCTGTGGCCTGGATGTCCCTTTATCCACGCTGGGCCCTGCAGTTATCATCTTCCATGAGAC T C ZFYVE1 Ensembl:ENSG00000165861 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs759886359 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1532421,Human_Splice_Rec_1532445,Human_Splice_Rec_1532467 RMVar_hsa_circ_84141,RMVar_hsa_circ_167730,RMVar_hsa_circ_101948,RMVar_hsa_circ_167732,RMVar_hsa_circ_117999,RMVar_hsa_circ_29373,RMVar_hsa_circ_53208,RMVar_hsa_circ_167733,RMVar_hsa_circ_274087,RMVar_hsa_circ_167739,RMVar_hsa_circ_167738,RMVar_hsa_circ_91363 16657 RMVar_ID_16657 Human_SNP_ID_560406195 A-to-I Human chr14 - 73003588 73003588 73003588 CTCCTGTCCCAGCCTCCTGAGTAGCTAGGACTATAGGCGTGAACCACTACGCCCAGCTAATTTTT CTCCTGTCCCAGCCTCCTGAGTAGCTAGGACTGTAGGCGTGAACCACTACGCCCAGCTAATTTTT T C ZFYVE1 Ensembl:ENSG00000165861 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs961253558 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29373 16658 RMVar_ID_16658 Human_SNP_ID_560429024 A-to-I Human chr14 + 73086192 73086192 73086192 GGTTTGGGATGGGTGTGGTGGCTCGAGCTTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGCGG GGTTTGGGATGGGTGTGGTGGCTCGAGCTTGTGATCCCAGCACTTTGGGAGGCTGAGGCAGGCGG A G RBM25 Ensembl:ENSG00000119707 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1338666554 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_299172,RMVar_hsa_circ_80586,RMVar_hsa_circ_122456,RMVar_hsa_circ_167745,RMVar_hsa_circ_303445,RMVar_hsa_circ_167748,RMVar_hsa_circ_291520,RMVar_hsa_circ_294441,RMVar_hsa_circ_167749,RMVar_hsa_circ_167751,RMVar_hsa_circ_167750,RMVar_hsa_circ_167753,RMVar_hsa_circ_291855,RMVar_hsa_circ_367439 16659 RMVar_ID_16659 Human_SNP_ID_560429943 A-to-I Human chr14 + 73089454 73089454 73089454 TTGGCTCACTGCAACCTCTGCCTCCCGTGTTCAGGTGATTCTCCTGCCTCAGCCTCCTGAGTAGC TTGGCTCACTGCAACCTCTGCCTCCCGTGTTCGGGTGATTCTCCTGCCTCAGCCTCCTGAGTAGC A G RBM25 Ensembl:ENSG00000119707 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs895722541 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80586,RMVar_hsa_circ_122456,RMVar_hsa_circ_167748,RMVar_hsa_circ_291520,RMVar_hsa_circ_167754,RMVar_hsa_circ_167749,RMVar_hsa_circ_167750,RMVar_hsa_circ_367439 16660 RMVar_ID_16660 Human_SNP_ID_560430500 A-to-I Human chr14 + 73091386 73091386 73091386 ACAGGTATGCACCACCATACTGGCTAAGTTTTATATTTTTTGTTGAGATGAAGTTTCACTGTGTT ACAGGTATGCACCACCATACTGGCTAAGTTTTGTATTTTTTGTTGAGATGAAGTTTCACTGTGTT A G RBM25 Ensembl:ENSG00000119707 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs191019238 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6381628 RMVar_hsa_circ_80586,RMVar_hsa_circ_122456,RMVar_hsa_circ_167748,RMVar_hsa_circ_291520,RMVar_hsa_circ_167754,RMVar_hsa_circ_167749,RMVar_hsa_circ_167750,RMVar_hsa_circ_367439 16661 RMVar_ID_16661 Human_SNP_ID_560431427 A-to-I Human chr14 + 73094616 73094616 73094616 ACCATGCCCGGCTAATTTTTTGTGTTTTTAGTAGAGACGGGGTTTCACCATGTTAGCCAGGATGG ACCATGCCCGGCTAATTTTTTGTGTTTTTAGTGGAGACGGGGTTTCACCATGTTAGCCAGGATGG A G RBM25 Ensembl:ENSG00000119707 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs184540438 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80586,RMVar_hsa_circ_122456,RMVar_hsa_circ_167748,RMVar_hsa_circ_291520,RMVar_hsa_circ_167754,RMVar_hsa_circ_167749,RMVar_hsa_circ_167750,RMVar_hsa_circ_367439 16662 RMVar_ID_16662 Human_SNP_ID_560431573 A-to-I Human chr14 + 73094880 73094880 73094880 TGTGTGTGTGTGTTTTTGATGGGGGTGGAGACAGAGTCTCGCTCTGTCTCCCAGGCTGGAATGGA TGTGTGTGTGTGTTTTTGATGGGGGTGGAGACGGAGTCTCGCTCTGTCTCCCAGGCTGGAATGGA A G RBM25 Ensembl:ENSG00000119707 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1377848858 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_757095,Human_RBP_ID_3460555,Human_RBP_ID_23635185 RMVar_hsa_circ_80586,RMVar_hsa_circ_122456,RMVar_hsa_circ_167748,RMVar_hsa_circ_291520,RMVar_hsa_circ_167754,RMVar_hsa_circ_167749,RMVar_hsa_circ_167750,RMVar_hsa_circ_367439 16663 RMVar_ID_16663 Human_SNP_ID_560438087 A-to-I Human chr14 + 73118289 73118289 73118289 CTTGAGCCCAGGAGTTTGAGACCAGCCTGGGCAACATAGTGAGACCCTGTCTCTACTAAAAAGCA CTTGAGCCCAGGAGTTTGAGACCAGCCTGGGCGACATAGTGAGACCCTGTCTCTACTAAAAAGCA A G RBM25 Ensembl:ENSG00000119707 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1298660889 Functional Loss SNV dbSNP153 33..33 33 - - - 16664 RMVar_ID_16664 Human_SNP_ID_560438320 A-to-I Human chr14 + 73119206 73119206 73119206 AAGAACGTAGTAATTTAAGAAGAACTAAATATACAACTATGTAATAACAATACAGAATCTCATGT AAGAACGTAGTAATTTAAGAAGAACTAAATATGCAACTATGTAATAACAATACAGAATCTCATGT A G RBM25 Ensembl:ENSG00000119707 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1415899275 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18656008 16665 RMVar_ID_16665 Human_SNP_ID_560445243 A-to-I Human chr14 + 73145067 73145067 73145067 GGCACGAGCTACCATGCCCAGCTAATTTTTGTATATTTAGTATGGACAGGGCTTCACCATGTTGG GGCACGAGCTACCATGCCCAGCTAATTTTTGTGTATTTAGTATGGACAGGGCTTCACCATGTTGG A G PSEN1 Ensembl:ENSG00000080815 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270413901 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6382071,Human_RBP_ID_12413135 16666 RMVar_ID_16666 Human_SNP_ID_560445244 A-to-I Human chr14 + 73145069 73145069 73145069 CACGAGCTACCATGCCCAGCTAATTTTTGTATATTTAGTATGGACAGGGCTTCACCATGTTGGCC CACGAGCTACCATGCCCAGCTAATTTTTGTATGTTTAGTATGGACAGGGCTTCACCATGTTGGCC A G PSEN1 Ensembl:ENSG00000080815 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982733595 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6382071,Human_RBP_ID_12413135 16667 RMVar_ID_16667 Human_SNP_ID_560445314 A-to-I Human chr14 + 73145358 73145357 73145359 TTTTATTATTTTATTATTTGTTTTTTTGAGACAGGGTCTCACTCTGTCACTCAGGCTGGAGTGTA TTTTATTATTTTATTATTTGTTTTTTTGAGAC__GGTCTCACTCTGTCACTCAGGCTGGAGTGTA CAG C PSEN1 Ensembl:ENSG00000080815 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs976948086 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_24367916 16668 RMVar_ID_16668 Human_SNP_ID_560445365 A-to-I Human chr14 + 73145553 73145553 73145553 TAGAAACAGGGTTTCACCATGTTGGCCAGGCTAGTCACGAACTCCTGGCCTCAAGTAGTAACACC TAGAAACAGGGTTTCACCATGTTGGCCAGGCTGGTCACGAACTCCTGGCCTCAAGTAGTAACACC A G PSEN1 Ensembl:ENSG00000080815 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1039825011 Functional Loss SNV dbSNP153 33..33 33 - - - 16669 RMVar_ID_16669 Human_SNP_ID_560445473 A-to-I Human chr14 + 73146069 73146069 73146069 TTAGAGGTTCCAGTGAGCGAGATCGTGCCACTACATTGCAGCCTGGGTGACAGAGCAAGACTGTG TTAGAGGTTCCAGTGAGCGAGATCGTGCCACTGCATTGCAGCCTGGGTGACAGAGCAAGACTGTG A G PSEN1 Ensembl:ENSG00000080815 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1022883376 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1532925 16670 RMVar_ID_16670 Human_SNP_ID_560446853 A-to-I Human chr14 + 73151830 73151830 73151830 AGCTCAAGTGATCCACATGTCTTGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCTACTGCGC AGCTCAAGTGATCCACATGTCTTGGCCTCCCAGAGTGCTGGGATTACAGGTGTGAGCTACTGCGC A G PSEN1 Ensembl:ENSG00000080815 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs565216273 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167762,RMVar_hsa_circ_281918,RMVar_hsa_circ_287120,RMVar_hsa_circ_313474,RMVar_hsa_circ_318862,RMVar_hsa_circ_281737,RMVar_hsa_circ_281746,RMVar_hsa_circ_280024,RMVar_hsa_circ_82306,RMVar_hsa_circ_271393,RMVar_hsa_circ_167764,RMVar_hsa_circ_60156,RMVar_hsa_circ_167763,RMVar_hsa_circ_167758,RMVar_hsa_circ_167760,RMVar_hsa_circ_167761,RMVar_hsa_circ_167759,RMVar_hsa_circ_11604,RMVar_hsa_circ_167757 16671 RMVar_ID_16671 Human_SNP_ID_560447404 A-to-I Human chr14 + 73153806 73153806 73153806 GCGATCTCGGCTCACTGCAGCCTCTGCCTCCCAGGTTCAAGCGATTCTCCTGCCTTAGTCTCCCG GCGATCTCGGCTCACTGCAGCCTCTGCCTCCCGGGTTCAAGCGATTCTCCTGCCTTAGTCTCCCG A G PSEN1 Ensembl:ENSG00000080815 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs954637000 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167762,RMVar_hsa_circ_281918,RMVar_hsa_circ_287120,RMVar_hsa_circ_313474,RMVar_hsa_circ_318862,RMVar_hsa_circ_281737,RMVar_hsa_circ_281746,RMVar_hsa_circ_280024,RMVar_hsa_circ_82306,RMVar_hsa_circ_271393,RMVar_hsa_circ_167764,RMVar_hsa_circ_60156,RMVar_hsa_circ_167763,RMVar_hsa_circ_167758,RMVar_hsa_circ_167760,RMVar_hsa_circ_167761,RMVar_hsa_circ_167759,RMVar_hsa_circ_11604,RMVar_hsa_circ_167757 16672 RMVar_ID_16672 Human_SNP_ID_560447953 A-to-I Human chr14 + 73156233 73156233 73156233 TAGTAATTAACTGGGTGTGGTGGCATGTGCCTATAGTCCCAGGTACTTGGGAGGCTGAGGTCGGA TAGTAATTAACTGGGTGTGGTGGCATGTGCCTGTAGTCCCAGGTACTTGGGAGGCTGAGGTCGGA A G PSEN1 Ensembl:ENSG00000080815 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs575801257 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167762,RMVar_hsa_circ_281918,RMVar_hsa_circ_287120,RMVar_hsa_circ_313474,RMVar_hsa_circ_318862,RMVar_hsa_circ_281737,RMVar_hsa_circ_281746,RMVar_hsa_circ_280024,RMVar_hsa_circ_82306,RMVar_hsa_circ_271393,RMVar_hsa_circ_167764,RMVar_hsa_circ_60156,RMVar_hsa_circ_167763,RMVar_hsa_circ_167758,RMVar_hsa_circ_167760,RMVar_hsa_circ_167761,RMVar_hsa_circ_167759,RMVar_hsa_circ_11604,RMVar_hsa_circ_167757 16673 RMVar_ID_16673 Human_SNP_ID_560447954 A-to-I Human chr14 + 73156233 73156233 73156233 TAGTAATTAACTGGGTGTGGTGGCATGTGCCTATAGTCCCAGGTACTTGGGAGGCTGAGGTCGGA TAGTAATTAACTGGGTGTGGTGGCATGTGCCTTTAGTCCCAGGTACTTGGGAGGCTGAGGTCGGA A T PSEN1 Ensembl:ENSG00000080815 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs575801257 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167762,RMVar_hsa_circ_281918,RMVar_hsa_circ_287120,RMVar_hsa_circ_313474,RMVar_hsa_circ_318862,RMVar_hsa_circ_281737,RMVar_hsa_circ_281746,RMVar_hsa_circ_280024,RMVar_hsa_circ_82306,RMVar_hsa_circ_271393,RMVar_hsa_circ_167764,RMVar_hsa_circ_60156,RMVar_hsa_circ_167763,RMVar_hsa_circ_167758,RMVar_hsa_circ_167760,RMVar_hsa_circ_167761,RMVar_hsa_circ_167759,RMVar_hsa_circ_11604,RMVar_hsa_circ_167757 16674 RMVar_ID_16674 Human_SNP_ID_560454261 A-to-I Human chr14 + 73183187 73183187 73183187 TTGCTCAGGCTGGAGTGCAATGGTGCGATCTCAGCTCTCCACAACCTCCGCCTCTCAGGTTGAAG TTGCTCAGGCTGGAGTGCAATGGTGCGATCTCGGCTCTCCACAACCTCCGCCTCTCAGGTTGAAG A G PSEN1 Ensembl:ENSG00000080815 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1468420686 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2192,RMVar_hsa_circ_167762,RMVar_hsa_circ_287120,RMVar_hsa_circ_313474,RMVar_hsa_circ_318862,RMVar_hsa_circ_281737,RMVar_hsa_circ_281746,RMVar_hsa_circ_280024,RMVar_hsa_circ_82306,RMVar_hsa_circ_167758,RMVar_hsa_circ_167760,RMVar_hsa_circ_167761,RMVar_hsa_circ_167759,RMVar_hsa_circ_11604,RMVar_hsa_circ_167757,RMVar_hsa_circ_268223,RMVar_hsa_circ_280768,RMVar_hsa_circ_332137,RMVar_hsa_circ_15742,RMVar_hsa_circ_167770 16675 RMVar_ID_16675 Human_SNP_ID_560457252 A-to-I Human chr14 + 73193055 73193055 73193055 GATTTCGGCTGGGCATGGTAGCTCATGCCTGTAATCTTAGCACTTTGGGAGGCTGAGGCGGGCAG GATTTCGGCTGGGCATGGTAGCTCATGCCTGTGATCTTAGCACTTTGGGAGGCTGAGGCGGGCAG A G PSEN1 Ensembl:ENSG00000080815 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1293760578 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2192,RMVar_hsa_circ_287120,RMVar_hsa_circ_318862,RMVar_hsa_circ_281746,RMVar_hsa_circ_280024,RMVar_hsa_circ_82306,RMVar_hsa_circ_167758,RMVar_hsa_circ_167760,RMVar_hsa_circ_167759,RMVar_hsa_circ_167757,RMVar_hsa_circ_268223,RMVar_hsa_circ_332137,RMVar_hsa_circ_15742,RMVar_hsa_circ_116653,RMVar_hsa_circ_315567,RMVar_hsa_circ_33890,RMVar_hsa_circ_167771,RMVar_hsa_circ_324882 16676 RMVar_ID_16676 Human_SNP_ID_560457267 A-to-I Human chr14 + 73193126 73193126 73193126 TAAGCCCAGAGTTCAAGACCAGCCTGGGCAACATGGCAAAACCTCGTATCTACAGAAAATACAAA TAAGCCCAGAGTTCAAGACCAGCCTGGGCAACGTGGCAAAACCTCGTATCTACAGAAAATACAAA A G PSEN1 Ensembl:ENSG00000080815 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs566742120 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2192,RMVar_hsa_circ_287120,RMVar_hsa_circ_318862,RMVar_hsa_circ_281746,RMVar_hsa_circ_280024,RMVar_hsa_circ_82306,RMVar_hsa_circ_167758,RMVar_hsa_circ_167760,RMVar_hsa_circ_167759,RMVar_hsa_circ_167757,RMVar_hsa_circ_268223,RMVar_hsa_circ_332137,RMVar_hsa_circ_15742,RMVar_hsa_circ_116653,RMVar_hsa_circ_315567,RMVar_hsa_circ_33890,RMVar_hsa_circ_167771,RMVar_hsa_circ_324882 16677 RMVar_ID_16677 Human_SNP_ID_560457310 A-to-I Human chr14 + 73193259 73193259 73193259 TTGAGCCCAGGAGGTCAAGGCTGCAGTGAGCCATGATTGCATCACTGTATTCCAGCCTGGGTGAT TTGAGCCCAGGAGGTCAAGGCTGCAGTGAGCCGTGATTGCATCACTGTATTCCAGCCTGGGTGAT A G PSEN1 Ensembl:ENSG00000080815 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1316859181 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2192,RMVar_hsa_circ_287120,RMVar_hsa_circ_318862,RMVar_hsa_circ_281746,RMVar_hsa_circ_280024,RMVar_hsa_circ_82306,RMVar_hsa_circ_167758,RMVar_hsa_circ_167760,RMVar_hsa_circ_167759,RMVar_hsa_circ_167757,RMVar_hsa_circ_268223,RMVar_hsa_circ_332137,RMVar_hsa_circ_15742,RMVar_hsa_circ_116653,RMVar_hsa_circ_315567,RMVar_hsa_circ_33890,RMVar_hsa_circ_167771,RMVar_hsa_circ_324882 16678 RMVar_ID_16678 Human_SNP_ID_560457349 A-to-I Human chr14 + 73193398 73193398 73193398 GAAACCCCGTCTCTACTAAAAATACAAAAATTAGCTGGGTGTGGTGGCGTACCCTTGTATTCCCA GAAACCCCGTCTCTACTAAAAATACAAAAATTGGCTGGGTGTGGTGGCGTACCCTTGTATTCCCA A G PSEN1 Ensembl:ENSG00000080815 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1240390108 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2192,RMVar_hsa_circ_287120,RMVar_hsa_circ_318862,RMVar_hsa_circ_281746,RMVar_hsa_circ_280024,RMVar_hsa_circ_82306,RMVar_hsa_circ_167758,RMVar_hsa_circ_167760,RMVar_hsa_circ_167759,RMVar_hsa_circ_167757,RMVar_hsa_circ_268223,RMVar_hsa_circ_332137,RMVar_hsa_circ_15742,RMVar_hsa_circ_116653,RMVar_hsa_circ_315567,RMVar_hsa_circ_33890,RMVar_hsa_circ_167771,RMVar_hsa_circ_324882 16679 RMVar_ID_16679 Human_SNP_ID_560457435 A-to-I Human chr14 + 73193680 73193680 73193680 TACTGCAGAAGCTTTTTTCTTTTTTTTGAGACAAAGTCTTGCTGTGTCACCCAGGCTGGGGTGCA TACTGCAGAAGCTTTTTTCTTTTTTTTGAGACGAAGTCTTGCTGTGTCACCCAGGCTGGGGTGCA A G PSEN1 Ensembl:ENSG00000080815 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1224184084 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17562597 RMVar_hsa_circ_2192,RMVar_hsa_circ_287120,RMVar_hsa_circ_318862,RMVar_hsa_circ_281746,RMVar_hsa_circ_280024,RMVar_hsa_circ_82306,RMVar_hsa_circ_167758,RMVar_hsa_circ_167760,RMVar_hsa_circ_167759,RMVar_hsa_circ_167757,RMVar_hsa_circ_268223,RMVar_hsa_circ_332137,RMVar_hsa_circ_15742,RMVar_hsa_circ_116653,RMVar_hsa_circ_315567,RMVar_hsa_circ_33890,RMVar_hsa_circ_167771,RMVar_hsa_circ_324882 16680 RMVar_ID_16680 Human_SNP_ID_560457471 A-to-I Human chr14 + 73193844 73193844 73193844 ATGCCTGACTAACTTGTTTATTTTTTGTAGAGAGAACGTCTTGCTATATTGCCTAGGCTGGTCTT ATGCCTGACTAACTTGTTTATTTTTTGTAGAGGGAACGTCTTGCTATATTGCCTAGGCTGGTCTT A G PSEN1 Ensembl:ENSG00000080815 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1267666648 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12413690 RMVar_hsa_circ_2192,RMVar_hsa_circ_287120,RMVar_hsa_circ_318862,RMVar_hsa_circ_281746,RMVar_hsa_circ_280024,RMVar_hsa_circ_82306,RMVar_hsa_circ_167758,RMVar_hsa_circ_167760,RMVar_hsa_circ_167759,RMVar_hsa_circ_167757,RMVar_hsa_circ_268223,RMVar_hsa_circ_332137,RMVar_hsa_circ_15742,RMVar_hsa_circ_116653,RMVar_hsa_circ_315567,RMVar_hsa_circ_33890,RMVar_hsa_circ_167771,RMVar_hsa_circ_324882 16681 RMVar_ID_16681 Human_SNP_ID_560481182 A-to-I Human chr14 - 73277936 73277936 73277936 CTCTTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGATGCATACCACCACGCCCAGCTAATTTTT CTCTTGCCTCAGCCTCCCGAGTAGCTGGGACTCCAGATGCATACCACCACGCCCAGCTAATTTTT T G NUMB Ensembl:ENSG00000133961 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956908727 Functional Loss SNV dbSNP153 33..33 33 - - - 16682 RMVar_ID_16682 Human_SNP_ID_560481190 A-to-I Human chr14 - 73277971 73277971 73277971 TCACTGCACCCTCTGCCTCTCAGGTTCAAGCAACTCTCTTGCCTCAGCCTCCCGAGTAGCTGGGA TCACTGCACCCTCTGCCTCTCAGGTTCAAGCAGCTCTCTTGCCTCAGCCTCCCGAGTAGCTGGGA T C NUMB Ensembl:ENSG00000133961 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1238308718 Functional Loss SNV dbSNP153 33..33 33 - - - 16683 RMVar_ID_16683 Human_SNP_ID_560481361 A-to-I Human chr14 - 73278363 73278363 73278363 GGTGCATGCCACCATGCCCAACCAATTTTTGTATTTTTAGTAGAAATGGGGTGTCACCATGTTGG GGTGCATGCCACCATGCCCAACCAATTTTTGTCTTTTTAGTAGAAATGGGGTGTCACCATGTTGG T G NUMB Ensembl:ENSG00000133961 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1423084197 Functional Loss SNV dbSNP153 33..33 33 - - - 16684 RMVar_ID_16684 Human_SNP_ID_560481509 A-to-I Human chr14 - 73278813 73278813 73278813 CGAGGCAGGAGAATCGCTTGAACCTGGGAGACAGAGTTTGCCGTGAGCCAAGATTGCGCCACTGC CGAGGCAGGAGAATCGCTTGAACCTGGGAGACGGAGTTTGCCGTGAGCCAAGATTGCGCCACTGC T C NUMB Ensembl:ENSG00000133961 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1383900936 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25112887 16685 RMVar_ID_16685 Human_SNP_ID_560483355 A-to-I Human chr14 - 73286297 73286297 73286297 ATAGTGGCTTACAGCTGTAATCTCAATACTTTAGGAGGCTGAGGAGGAAACATCACTTGAGGCCA ATAGTGGCTTACAGCTGTAATCTCAATACTTTGGGAGGCTGAGGAGGAAACATCACTTGAGGCCA T C NUMB Ensembl:ENSG00000133961 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1135462 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113376,RMVar_hsa_circ_46635,RMVar_hsa_circ_167777,RMVar_hsa_circ_343298,RMVar_hsa_circ_274715,RMVar_hsa_circ_308619,RMVar_hsa_circ_61541,RMVar_hsa_circ_167779,RMVar_hsa_circ_167778,RMVar_hsa_circ_167780 16686 RMVar_ID_16686 Human_SNP_ID_560483362 A-to-I Human chr14 - 73286317 73286317 73286317 ATATAATTTTGAGGCCAGGTATAGTGGCTTACAGCTGTAATCTCAATACTTTAGGAGGCTGAGGA ATATAATTTTGAGGCCAGGTATAGTGGCTTACGGCTGTAATCTCAATACTTTAGGAGGCTGAGGA T C NUMB Ensembl:ENSG00000133961 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1057542 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113376,RMVar_hsa_circ_46635,RMVar_hsa_circ_167777,RMVar_hsa_circ_343298,RMVar_hsa_circ_274715,RMVar_hsa_circ_308619,RMVar_hsa_circ_61541,RMVar_hsa_circ_167779,RMVar_hsa_circ_167778,RMVar_hsa_circ_167780 16687 RMVar_ID_16687 Human_SNP_ID_560485349 A-to-I Human chr14 - 73294658 73294656 73294658 AAAAAATTCGCTGGGCATGGTGGTGCGTGCCTATGGTTCCAGCTACTTGGGAGGCTGAGGCATGA AAAAAATTCGCTGGGCATGGTGGTGCGTGCCTGTAGTTCCAGCTACTTGGGAGGCTGAGGCATGA CAT TAC NUMB Ensembl:ENSG00000133961 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1566730506 Functional Loss MNV dbSNP153 33..35 33 - - - RMVar_hsa_circ_44470,RMVar_hsa_circ_113376,RMVar_hsa_circ_46635,RMVar_hsa_circ_274715,RMVar_hsa_circ_167779,RMVar_hsa_circ_167780,RMVar_hsa_circ_358477,RMVar_hsa_circ_310303,RMVar_hsa_circ_167783,RMVar_hsa_circ_70583,RMVar_hsa_circ_21881,RMVar_hsa_circ_39660,RMVar_hsa_circ_4655 16688 RMVar_ID_16688 Human_SNP_ID_560485350 A-to-I Human chr14 - 73294658 73294658 73294658 AAAAAATTCGCTGGGCATGGTGGTGCGTGCCTATGGTTCCAGCTACTTGGGAGGCTGAGGCATGA AAAAAATTCGCTGGGCATGGTGGTGCGTGCCTGTGGTTCCAGCTACTTGGGAGGCTGAGGCATGA T C NUMB Ensembl:ENSG00000133961 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs75488375 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44470,RMVar_hsa_circ_113376,RMVar_hsa_circ_46635,RMVar_hsa_circ_274715,RMVar_hsa_circ_167779,RMVar_hsa_circ_167780,RMVar_hsa_circ_358477,RMVar_hsa_circ_310303,RMVar_hsa_circ_167783,RMVar_hsa_circ_70583,RMVar_hsa_circ_21881,RMVar_hsa_circ_39660,RMVar_hsa_circ_4655 16689 RMVar_ID_16689 Human_SNP_ID_560486244 A-to-I Human chr14 - 73298021 73298021 73298021 AGCCGGGCATGGTGGCAGGTGCCTGTAATCCCAGCTAGTCGGGAGGCTGAGGCAGGAGAATCACT AGCCGGGCATGGTGGCAGGTGCCTGTAATCCCTGCTAGTCGGGAGGCTGAGGCAGGAGAATCACT T A NUMB Ensembl:ENSG00000133961 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs899928452 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44470,RMVar_hsa_circ_113376,RMVar_hsa_circ_46635,RMVar_hsa_circ_167780,RMVar_hsa_circ_358477,RMVar_hsa_circ_70583,RMVar_hsa_circ_21881,RMVar_hsa_circ_4655 16690 RMVar_ID_16690 Human_SNP_ID_560486245 A-to-I Human chr14 - 73298021 73298021 73298021 AGCCGGGCATGGTGGCAGGTGCCTGTAATCCCAGCTAGTCGGGAGGCTGAGGCAGGAGAATCACT AGCCGGGCATGGTGGCAGGTGCCTGTAATCCCGGCTAGTCGGGAGGCTGAGGCAGGAGAATCACT T C NUMB Ensembl:ENSG00000133961 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs899928452 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44470,RMVar_hsa_circ_113376,RMVar_hsa_circ_46635,RMVar_hsa_circ_167780,RMVar_hsa_circ_358477,RMVar_hsa_circ_70583,RMVar_hsa_circ_21881,RMVar_hsa_circ_4655 16691 RMVar_ID_16691 Human_SNP_ID_560486628 A-to-I Human chr14 - 73299609 73299607 73299609 CTAGGAGATATGTCATATTATATGACATATATATGTCATATCATATATATGACATGACATATGTC CTAGGAGATATGTCATATTATATGACATATAT__GTCATATCATATATATGACATGACATATGTC CAT C NUMB Ensembl:ENSG00000133961 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1409942000 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_44470,RMVar_hsa_circ_113376,RMVar_hsa_circ_46635,RMVar_hsa_circ_167780,RMVar_hsa_circ_358477,RMVar_hsa_circ_70583,RMVar_hsa_circ_21881,RMVar_hsa_circ_4655 16692 RMVar_ID_16692 Human_SNP_ID_560486630 A-to-I Human chr14 - 73299611 73299611 73299611 CGCTAGGAGATATGTCATATTATATGACATATATATGTCATATCATATATATGACATGACATATG CGCTAGGAGATATGTCATATTATATGACATATGTATGTCATATCATATATATGACATGACATATG T C NUMB Ensembl:ENSG00000133961 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1159037428 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44470,RMVar_hsa_circ_113376,RMVar_hsa_circ_46635,RMVar_hsa_circ_167780,RMVar_hsa_circ_358477,RMVar_hsa_circ_70583,RMVar_hsa_circ_21881,RMVar_hsa_circ_4655 16693 RMVar_ID_16693 Human_SNP_ID_560487043 A-to-I Human chr14 - 73301530 73301530 73301530 GGGAGGCTGAAGTGGGAGAATTACTGGAGCCCAGGAGTTCAAGGCTGCAGTGAGCTGTCCTGTGC GGGAGGCTGAAGTGGGAGAATTACTGGAGCCCGGGAGTTCAAGGCTGCAGTGAGCTGTCCTGTGC T C NUMB Ensembl:ENSG00000133961 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1294396943 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44470,RMVar_hsa_circ_113376,RMVar_hsa_circ_46635,RMVar_hsa_circ_167780,RMVar_hsa_circ_358477,RMVar_hsa_circ_70583,RMVar_hsa_circ_21881,RMVar_hsa_circ_4655 16694 RMVar_ID_16694 Human_SNP_ID_560487062 A-to-I Human chr14 - 73301623 73301623 73301623 CAGCCTAGGCAGCAGGGCAAGACCCTGTCTCTACAAAAAATTGTTTAAAAATTAGCTGGGTATGG CAGCCTAGGCAGCAGGGCAAGACCCTGTCTCTGCAAAAAATTGTTTAAAAATTAGCTGGGTATGG T C NUMB Ensembl:ENSG00000133961 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs555892910 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44470,RMVar_hsa_circ_113376,RMVar_hsa_circ_46635,RMVar_hsa_circ_167780,RMVar_hsa_circ_358477,RMVar_hsa_circ_70583,RMVar_hsa_circ_21881,RMVar_hsa_circ_4655 16695 RMVar_ID_16695 Human_SNP_ID_560487513 A-to-I Human chr14 - 73303456 73303456 73303456 CCTGCCACAGCCTCCAGAGCAGCTGGGACTACAGGCGCATGTCACCACGCCCGGCTGATTTTTGT CCTGCCACAGCCTCCAGAGCAGCTGGGACTACTGGCGCATGTCACCACGCCCGGCTGATTTTTGT T A NUMB Ensembl:ENSG00000133961 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs916161457 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44470,RMVar_hsa_circ_113376,RMVar_hsa_circ_46635,RMVar_hsa_circ_167780,RMVar_hsa_circ_358477,RMVar_hsa_circ_70583,RMVar_hsa_circ_21881,RMVar_hsa_circ_4655 16696 RMVar_ID_16696 Human_SNP_ID_560489447 A-to-I Human chr14 - 73312311 73312311 73312311 CTCGGTCACTGCAACCTCTGCTTTCTGGGTTCAGGTGATTTTTTGCTTCAGCCTCCCAAGTAGCT CTCGGTCACTGCAACCTCTGCTTTCTGGGTTCGGGTGATTTTTTGCTTCAGCCTCCCAAGTAGCT T C NUMB Ensembl:ENSG00000133961 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs887483299 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44470,RMVar_hsa_circ_113376,RMVar_hsa_circ_46635,RMVar_hsa_circ_167780,RMVar_hsa_circ_358477,RMVar_hsa_circ_70583,RMVar_hsa_circ_21881,RMVar_hsa_circ_4655 16697 RMVar_ID_16697 Human_SNP_ID_560491782 A-to-I Human chr14 - 73322985 73322985 73322985 TGTGGGCTTGCTAATAAGGAGCATCTCAGCCAAGCGCGGTGGCTCACTCCTGTAATCCTAGCACT TGTGGGCTTGCTAATAAGGAGCATCTCAGCCACGCGCGGTGGCTCACTCCTGTAATCCTAGCACT T G NUMB Ensembl:ENSG00000133961 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904369641 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113376,RMVar_hsa_circ_46635,RMVar_hsa_circ_167780,RMVar_hsa_circ_358477,RMVar_hsa_circ_70583,RMVar_hsa_circ_29789,RMVar_hsa_circ_21881,RMVar_hsa_circ_4655,RMVar_hsa_circ_369017 16698 RMVar_ID_16698 Human_SNP_ID_560510192 A-to-I Human chr14 - 73396480 73396480 73396480 AGCCAGGCCTTGTGGTATGGGCCTGTAGTCCCAGCTGCTCTGGAGGCTGAGGTGGGAAGATCCCT AGCCAGGCCTTGTGGTATGGGCCTGTAGTCCCGGCTGCTCTGGAGGCTGAGGTGGGAAGATCCCT T C NUMB,AC005280.3 Ensembl:ENSG00000133961,Ensembl:ENSG00000285006 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335141756 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70583,RMVar_hsa_circ_361170,RMVar_hsa_circ_289123,RMVar_hsa_circ_167787 16699 RMVar_ID_16699 Human_SNP_ID_560516023 A-to-I Human chr14 - 73419343 73419343 73419343 ACCACACCCAGCTAGTTTTTTGTATTTTTAGTAGAGACCGGGTTTCACCGTGTTAGCCAGGATTG ACCACACCCAGCTAGTTTTTTGTATTTTTAGTGGAGACCGGGTTTCACCGTGTTAGCCAGGATTG T C NUMB,AC005280.3 Ensembl:ENSG00000133961,Ensembl:ENSG00000285006 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs565791441 Functional Loss SNV dbSNP153 33..33 33 - - - 16700 RMVar_ID_16700 Human_SNP_ID_560517629 A-to-I Human chr14 - 73425973 73425973 73425973 AAACATTGTATCTACTAAAAATACAAAAAATTAGCTGGGCTTGGTGGCACGTACCTGTAGTCCCA AAACATTGTATCTACTAAAAATACAAAAAATTGGCTGGGCTTGGTGGCACGTACCTGTAGTCCCA T C NUMB,AC005280.3 Ensembl:ENSG00000133961,Ensembl:ENSG00000285006 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs746141243 Functional Loss SNV dbSNP153 33..33 33 - - - 16701 RMVar_ID_16701 Human_SNP_ID_560520363 A-to-I Human chr14 - 73437148 73437148 73437148 CCAGCTACTCGGGAGGCTGAGGTGGGAGGATCACTTGAGCCCAGGAGGTTGAGGCTGCTGTGAGT CCAGCTACTCGGGAGGCTGAGGTGGGAGGATCGCTTGAGCCCAGGAGGTTGAGGCTGCTGTGAGT T C NUMB,AC005280.3 Ensembl:ENSG00000133961,Ensembl:ENSG00000285006 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1366028440 Functional Loss SNV dbSNP153 33..33 33 - - - 16702 RMVar_ID_16702 Human_SNP_ID_560523018 A-to-I Human chr14 - 73447004 73447004 73447004 TTTTTGTATTTTAGTAGAGACTGGGTTTCACTATGTTGGCCAGGTTAGTCTCAATCTTCTGACCT TTTTTGTATTTTAGTAGAGACTGGGTTTCACTGTGTTGGCCAGGTTAGTCTCAATCTTCTGACCT T C NUMB,AC005280.3 Ensembl:ENSG00000133961,Ensembl:ENSG00000285006 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1023493217 Functional Loss SNV dbSNP153 33..33 33 - - - 16703 RMVar_ID_16703 Human_SNP_ID_560535483 A-to-I Human chr14 + 73494690 73494690 73494690 CTCCCATCTCAGCCTCCTTAGTAGATAGGACTACCAGTGTGTGCCACCACACCCAGATAATTTTT CTCCCATCTCAGCCTCCTTAGTAGATAGGACTGCCAGTGTGTGCCACCACACCCAGATAATTTTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270798547 Functional Loss SNV dbSNP153 33..33 33 - - - 16704 RMVar_ID_16704 Human_SNP_ID_560544849 A-to-I Human chr14 + 73530201 73530201 73530201 GTTGTCCAGGCTGGTTTCAAACTCCTGGAATCAAGCGATCTTCCTGCCTTGGCCTCCAGAAATGC GTTGTCCAGGCTGGTTTCAAACTCCTGGAATCTAGCGATCTTCCTGCCTTGGCCTCCAGAAATGC A T AC005225.3 Ensembl:ENSG00000258695 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1216806514 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1533876 16705 RMVar_ID_16705 Human_SNP_ID_560551934 A-to-I Human chr14 - 73565547 73565546 73565547 AGAAGGAACGAACTCTGGACATGCCACCTTTAAGAGCTGTAATGCTCCCGTGAGGGTCCACGGCT AGAAGGAACGAACTCTGGACATGCCACCTTTA_GAGCTGTAATGCTCCCGTGAGGGTCCACGGCT CT C AC005225.2 Ensembl:ENSG00000258603 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1254761177 Functional Loss DEL dbSNP153 33..33 33 - - - 16706 RMVar_ID_16706 Human_SNP_ID_560552509 A-to-I Human chr14 - 73567610 73567610 73567610 CTGGAGCGGAACTCACGCAGGTTACCACTACTAGCTGGGGTGACCAGCTTTTATTCCCTTATTTG CTGGAGCGGAACTCACGCAGGTTACCACTACTGGCTGGGGTGACCAGCTTTTATTCCCTTATTTG T C AC005225.2 Ensembl:ENSG00000258603 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1021159377 Functional Loss SNV dbSNP153 33..33 33 - - - 16707 RMVar_ID_16707 Human_SNP_ID_560552514 A-to-I Human chr14 - 73567619 73567619 73567619 TCCATCAGCCTGGAGCGGAACTCACGCAGGTTACCACTACTAGCTGGGGTGACCAGCTTTTATTC TCCATCAGCCTGGAGCGGAACTCACGCAGGTTGCCACTACTAGCTGGGGTGACCAGCTTTTATTC T C AC005225.2 Ensembl:ENSG00000258603 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs906355639 Functional Loss SNV dbSNP153 33..33 33 - - - 16708 RMVar_ID_16708 Human_SNP_ID_560552534 A-to-I Human chr14 - 73567683 73567683 73567683 TGCAGTATGGACCCAAAGAAGGAGCAGTAGCAAGGTTTATTGTGAAGTACAAAAGAACAAAGCTT TGCAGTATGGACCCAAAGAAGGAGCAGTAGCAGGGTTTATTGTGAAGTACAAAAGAACAAAGCTT T C AC005225.2 Ensembl:ENSG00000258603 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1443796378 Functional Loss SNV dbSNP153 33..33 33 - - - 16709 RMVar_ID_16709 Human_SNP_ID_560555225 A-to-I Human chr14 - 73575302 73575302 73575302 CAATATAGTGCCCTGTCTCTGGGTAACAGATGATCTGGGGCTTTCTCCTCCCATGGGCCTGCAAG CAATATAGTGCCCTGTCTCTGGGTAACAGATGGTCTGGGGCTTTCTCCTCCCATGGGCCTGCAAG T C AC005225.2 Ensembl:ENSG00000258603 lincRNA intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1450664198 Functional Loss SNV dbSNP153 33..33 33 - - - 16710 RMVar_ID_16710 Human_SNP_ID_560566868 A-to-I Human chr14 - 73616091 73616091 73616091 ATGATGGCACTTGCCTATAGTCTTAGCTACTCAGGAGGAAGAGGCGGGAGGATCATCTGAGCCCA ATGATGGCACTTGCCTATAGTCTTAGCTACTCGGGAGGAAGAGGCGGGAGGATCATCTGAGCCCA T C AC005225.2 Ensembl:ENSG00000258603 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs556097696 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_50 16711 RMVar_ID_16711 Human_SNP_ID_560566889 A-to-I Human chr14 - 73616166 73616166 73616166 GCCAGGAATTCACGACCAGCCTGGGCAACATAACAAGACCCATCTCTACAAAAAAGTTTAAAAAA GCCAGGAATTCACGACCAGCCTGGGCAACATATCAAGACCCATCTCTACAAAAAAGTTTAAAAAA T A AC005225.2 Ensembl:ENSG00000258603 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs891288104 Functional Loss SNV dbSNP153 33..33 33 - - - 16712 RMVar_ID_16712 Human_SNP_ID_560580510 A-to-I Human chr14 + 73673770 73673770 73673770 AAGAAATTAGCCAGGCATGGTGGTACATGCCTATAGTCCCAGCTACTCGGGGAGGCTGAGGTGGA AAGAAATTAGCCAGGCATGGTGGTACATGCCTGTAGTCCCAGCTACTCGGGGAGGCTGAGGTGGA A G DNAL1 Ensembl:ENSG00000119661 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1186159132 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_334024,RMVar_hsa_circ_343939,RMVar_hsa_circ_342797,RMVar_hsa_circ_167795,RMVar_hsa_circ_285580,RMVar_hsa_circ_167796,RMVar_hsa_circ_378844,RMVar_hsa_circ_20139,RMVar_hsa_circ_167800,RMVar_hsa_circ_327381,RMVar_hsa_circ_167798,RMVar_hsa_circ_310148,RMVar_hsa_circ_167799 16713 RMVar_ID_16713 Human_SNP_ID_560580528 A-to-I Human chr14 + 73673847 73673847 73673847 TTGAGCCTAGGAGTTTGAGTTTACAGTGAACTATGATTGTGCCATAGCAATGCAGTCTGGGTGAC TTGAGCCTAGGAGTTTGAGTTTACAGTGAACTGTGATTGTGCCATAGCAATGCAGTCTGGGTGAC A G DNAL1 Ensembl:ENSG00000119661 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1304216655 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_334024,RMVar_hsa_circ_343939,RMVar_hsa_circ_342797,RMVar_hsa_circ_167795,RMVar_hsa_circ_285580,RMVar_hsa_circ_167796,RMVar_hsa_circ_378844,RMVar_hsa_circ_20139,RMVar_hsa_circ_167800,RMVar_hsa_circ_327381,RMVar_hsa_circ_167798,RMVar_hsa_circ_310148,RMVar_hsa_circ_167799 16714 RMVar_ID_16714 Human_SNP_ID_560581925 A-to-I Human chr14 + 73678756 73678756 73678756 AACATAGCTTATACAAAAGACTGCAACAATCTAAGTGTCTATCAGCAGTGGACTAGCTAAATATA AACATAGCTTATACAAAAGACTGCAACAATCTGAGTGTCTATCAGCAGTGGACTAGCTAAATATA A G DNAL1 Ensembl:ENSG00000119661 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900376251 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_334024,RMVar_hsa_circ_343939,RMVar_hsa_circ_342797,RMVar_hsa_circ_167795,RMVar_hsa_circ_285580,RMVar_hsa_circ_167796,RMVar_hsa_circ_378844,RMVar_hsa_circ_20139,RMVar_hsa_circ_167800,RMVar_hsa_circ_327381,RMVar_hsa_circ_167798,RMVar_hsa_circ_310148,RMVar_hsa_circ_167799 16715 RMVar_ID_16715 Human_SNP_ID_560581930 A-to-I Human chr14 + 73678767 73678767 73678767 TACAAAAGACTGCAACAATCTAAGTGTCTATCAGCAGTGGACTAGCTAAATATATTAATAAATAC TACAAAAGACTGCAACAATCTAAGTGTCTATCGGCAGTGGACTAGCTAAATATATTAATAAATAC A G DNAL1 Ensembl:ENSG00000119661 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054897814 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_334024,RMVar_hsa_circ_343939,RMVar_hsa_circ_342797,RMVar_hsa_circ_167795,RMVar_hsa_circ_285580,RMVar_hsa_circ_167796,RMVar_hsa_circ_378844,RMVar_hsa_circ_20139,RMVar_hsa_circ_167800,RMVar_hsa_circ_327381,RMVar_hsa_circ_167798,RMVar_hsa_circ_310148,RMVar_hsa_circ_167799 16716 RMVar_ID_16716 Human_SNP_ID_560587393 A-to-I Human chr14 + 73700198 73700197 73700199 ACGTGGTGAAACCCCATGTCTACCAAAAATATAAAAAGATAGCCGGGCGTGGTGGCGCATGCCTG ACGTGGTGAAACCCCATGTCTACCAAAAATAT__AAAGATAGCCGGGCGTGGTGGCGCATGCCTG TAA T DNAL1 Ensembl:ENSG00000119661 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1218896294 Functional Loss DEL dbSNP153 33..34 33 - - - 16717 RMVar_ID_16717 Human_SNP_ID_560587395 A-to-I Human chr14 + 73700206 73700206 73700206 AAACCCCATGTCTACCAAAAATATAAAAAGATAGCCGGGCGTGGTGGCGCATGCCTGTAATCCCA AAACCCCATGTCTACCAAAAATATAAAAAGATGGCCGGGCGTGGTGGCGCATGCCTGTAATCCCA A G DNAL1 Ensembl:ENSG00000119661 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1357792536 Functional Loss SNV dbSNP153 33..33 33 - - - 16718 RMVar_ID_16718 Human_SNP_ID_560587435 A-to-I Human chr14 + 73700335 73700335 73700335 AAATAGTGTGACTGTACTCCAGCCTGGGTGACAGAGTAAGTCTCCGTCTCAAAAAGAAAAAAAAA AAATAGTGTGACTGTACTCCAGCCTGGGTGACGGAGTAAGTCTCCGTCTCAAAAAGAAAAAAAAA A G DNAL1 Ensembl:ENSG00000119661 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1324849538 Functional Loss SNV dbSNP153 33..33 33 - - - 16719 RMVar_ID_16719 Human_SNP_ID_560587436 A-to-I Human chr14 + 73700337 73700337 73700337 ATAGTGTGACTGTACTCCAGCCTGGGTGACAGAGTAAGTCTCCGTCTCAAAAAGAAAAAAAAAAA ATAGTGTGACTGTACTCCAGCCTGGGTGACAGGGTAAGTCTCCGTCTCAAAAAGAAAAAAAAAAA A G DNAL1 Ensembl:ENSG00000119661 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs986114293 Functional Loss SNV dbSNP153 33..33 33 - - - 16720 RMVar_ID_16720 Human_SNP_ID_560588145 A-to-I Human chr14 + 73703036 73703036 73703036 AGCTACTGGGGAGGCTGAGGCAGGATTGCTTGAACCCAGAAGTTTGAGGTTACAGTGAGCTATGA AGCTACTGGGGAGGCTGAGGCAGGATTGCTTGTACCCAGAAGTTTGAGGTTACAGTGAGCTATGA A T DNAL1 Ensembl:ENSG00000119661 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1352832760 Functional Loss SNV dbSNP153 33..33 33 - - - 16721 RMVar_ID_16721 Human_SNP_ID_560591621 A-to-I Human chr14 - 73714356 73714356 73714356 CTGCAGCAGTAACGTCGCGGCGGGTTGCGGGTAGGACTGGACGCCAGAGCAGCCGCGCAGCGCCT CTGCAGCAGTAACGTCGCGGCGGGTTGCGGGTGGGACTGGACGCCAGAGCAGCCGCGCAGCGCCT T C PNMA1 Ensembl:ENSG00000176903 Protein coding 5'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs889767437 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4301323,Human_RBP_ID_5418280,Human_RBP_ID_8796142,Human_RBP_ID_26927677 16722 RMVar_ID_16722 Human_SNP_ID_560596060 A-to-I Human chr14 - 73730141 73730141 73730141 TTTGCTGACTTCTGCCCTAGAGGAGATGATAAAAAGGGCTTTTGGACCTGCTCCTTTTTTCAGGC TTTGCTGACTTCTGCCCTAGAGGAGATGATAAGAAGGGCTTTTGGACCTGCTCCTTTTTTCAGGC T C MIDEAS Ensembl:ENSG00000156030 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6574140 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1534108,Human_Splice_Rec_1534109 Clinvar_Rec_51,Clinvar_Rec_52,Clinvar_Rec_53,Clinvar_Rec_54 GWAS_ID_1174,GWAS_ID_1175,GWAS_ID_1176,GWAS_ID_1177,GWAS_ID_1178,GWAS_ID_1179,GWAS_ID_1180,GWAS_ID_1181,GWAS_ID_1182 RMVar_hsa_circ_338810,RMVar_hsa_circ_351975 16723 RMVar_ID_16723 Human_SNP_ID_560596106 A-to-I Human chr14 - 73730278 73730278 73730278 TCCAGAGCTAAGAATGTGTTACAATTTTATACAGTTAGTTTTAAAAAGAAAAAGGGAAAGAAGAG TCCAGAGCTAAGAATGTGTTACAATTTTATACTGTTAGTTTTAAAAAGAAAAAGGGAAAGAAGAG T A MIDEAS Ensembl:ENSG00000156030 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4899477 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_55,Clinvar_Rec_56,Clinvar_Rec_57,Clinvar_Rec_58 GWAS_ID_1183,GWAS_ID_1184,GWAS_ID_1185,GWAS_ID_1186,GWAS_ID_1187,GWAS_ID_1188,GWAS_ID_1189,GWAS_ID_1190,GWAS_ID_1191 RMVar_hsa_circ_351975 16724 RMVar_ID_16724 Human_SNP_ID_560596107 A-to-I Human chr14 - 73730278 73730278 73730278 TCCAGAGCTAAGAATGTGTTACAATTTTATACAGTTAGTTTTAAAAAGAAAAAGGGAAAGAAGAG TCCAGAGCTAAGAATGTGTTACAATTTTATACGGTTAGTTTTAAAAAGAAAAAGGGAAAGAAGAG T C MIDEAS Ensembl:ENSG00000156030 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4899477 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_55,Clinvar_Rec_56,Clinvar_Rec_57,Clinvar_Rec_58 GWAS_ID_1183,GWAS_ID_1184,GWAS_ID_1185,GWAS_ID_1186,GWAS_ID_1187,GWAS_ID_1188,GWAS_ID_1189,GWAS_ID_1190,GWAS_ID_1191 RMVar_hsa_circ_351975 16725 RMVar_ID_16725 Human_SNP_ID_560596920 A-to-I Human chr14 - 73733768 73733768 73733768 ATCGCTTGAACCTGGGAGGTGGAGGTTGTAGTAAGCCAAGATCGTACCACTGCACTCCAGCTTGG ATCGCTTGAACCTGGGAGGTGGAGGTTGTAGTGAGCCAAGATCGTACCACTGCACTCCAGCTTGG T C MIDEAS Ensembl:ENSG00000156030 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1214448577 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_351975 16726 RMVar_ID_16726 Human_SNP_ID_560597126 A-to-I Human chr14 - 73734546 73734546 73734546 AAGATTAGCTGGGTGTGGTGGTGCACACCTGTAGTCCCAGTTTCTCAGGAGGCTGAGGTGGGAGG AAGATTAGCTGGGTGTGGTGGTGCACACCTGTGGTCCCAGTTTCTCAGGAGGCTGAGGTGGGAGG T C MIDEAS Ensembl:ENSG00000156030 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs145617040 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_351975 16727 RMVar_ID_16727 Human_SNP_ID_560598003 A-to-I Human chr14 - 73737933 73737933 73737933 ACCAAAAAACACAAAAATTAGCCAGGTGTGGTACTGCACGCCTGTAATCCCAGCTACTGGGGAGG ACCAAAAAACACAAAAATTAGCCAGGTGTGGTTCTGCACGCCTGTAATCCCAGCTACTGGGGAGG T A MIDEAS Ensembl:ENSG00000156030 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10135344 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_59,Clinvar_Rec_60,Clinvar_Rec_61,Clinvar_Rec_62 GWAS_ID_1192,GWAS_ID_1193,GWAS_ID_1194,GWAS_ID_1195,GWAS_ID_1196,GWAS_ID_1197,GWAS_ID_1198,GWAS_ID_1199,GWAS_ID_1200 RMVar_hsa_circ_167804,RMVar_hsa_circ_351975,RMVar_hsa_circ_311424,RMVar_hsa_circ_107985 16728 RMVar_ID_16728 Human_SNP_ID_560598004 A-to-I Human chr14 - 73737933 73737933 73737933 ACCAAAAAACACAAAAATTAGCCAGGTGTGGTACTGCACGCCTGTAATCCCAGCTACTGGGGAGG ACCAAAAAACACAAAAATTAGCCAGGTGTGGTGCTGCACGCCTGTAATCCCAGCTACTGGGGAGG T C MIDEAS Ensembl:ENSG00000156030 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10135344 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_59,Clinvar_Rec_60,Clinvar_Rec_61,Clinvar_Rec_62 GWAS_ID_1192,GWAS_ID_1193,GWAS_ID_1194,GWAS_ID_1195,GWAS_ID_1196,GWAS_ID_1197,GWAS_ID_1198,GWAS_ID_1199,GWAS_ID_1200 RMVar_hsa_circ_167804,RMVar_hsa_circ_351975,RMVar_hsa_circ_311424,RMVar_hsa_circ_107985 16729 RMVar_ID_16729 Human_SNP_ID_560598015 A-to-I Human chr14 - 73737971 73737971 73737971 GGAGACCAGCCTGGCCAACACAGCAAAACCCTATCTCTACCAAAAAACACAAAAATTAGCCAGGT GGAGACCAGCCTGGCCAACACAGCAAAACCCTGTCTCTACCAAAAAACACAAAAATTAGCCAGGT T C MIDEAS Ensembl:ENSG00000156030 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1387950745 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167804,RMVar_hsa_circ_351975,RMVar_hsa_circ_311424,RMVar_hsa_circ_107985 16730 RMVar_ID_16730 Human_SNP_ID_560598025 A-to-I Human chr14 - 73738059 73738059 73738059 CAGTGTGAGGCTAGGCGCAGTGGCTTATGCCTATAATCCCAGCACTTTGGGAGGCCAAGGTGGGT CAGTGTGAGGCTAGGCGCAGTGGCTTATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGT T C MIDEAS Ensembl:ENSG00000156030 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1187790659 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167804,RMVar_hsa_circ_351975,RMVar_hsa_circ_311424,RMVar_hsa_circ_107985 16731 RMVar_ID_16731 Human_SNP_ID_560598049 A-to-I Human chr14 - 73738147 73738146 73738148 GTGATCTGCCTGCCTCAGCCCCCCAAAGTGCTAGGATTACAGGCGTGAGCCACCGTGTCCAGCCA GTGATCTGCCTGCCTCAGCCCCCCAAAGTGC__GGATTACAGGCGTGAGCCACCGTGTCCAGCCA CTA C MIDEAS Ensembl:ENSG00000156030 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1431509987 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_167804,RMVar_hsa_circ_351975,RMVar_hsa_circ_311424,RMVar_hsa_circ_107985 16732 RMVar_ID_16732 Human_SNP_ID_560598073 A-to-I Human chr14 - 73738247 73738246 73738247 GGATTACAGGCGCCTGCCACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTTAC GGATTACAGGCGCCTGCCACCATGCCTGGCTA_TTTTTGTATTTTTAGTAGAGACAGGGTTTTAC AT A MIDEAS Ensembl:ENSG00000156030 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1173236665 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_167804,RMVar_hsa_circ_351975,RMVar_hsa_circ_311424,RMVar_hsa_circ_107985 16733 RMVar_ID_16733 Human_SNP_ID_560627227 A-to-I Human chr14 + 73853021 73853021 73853021 TTTTTGTATTTTTAGTAGAGCGGGGTTTTCCCATGTTGGCCAGACTGGTCTCGAATTCCTGGCCT TTTTTGTATTTTTAGTAGAGCGGGGTTTTCCCGTGTTGGCCAGACTGGTCTCGAATTCCTGGCCT A G PTGR2,AC005520.3 Ensembl:ENSG00000140043,Ensembl:ENSG00000258653 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1298962063 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12415701 16734 RMVar_ID_16734 Human_SNP_ID_560627238 A-to-I Human chr14 + 73853073 73853073 73853073 GAATTCCTGGCCTCAAGTGAGCCTCCCACCTCAGCCTCCCAAAGTGCTGGAATTACAGGTGTGAG GAATTCCTGGCCTCAAGTGAGCCTCCCACCTCGGCCTCCCAAAGTGCTGGAATTACAGGTGTGAG A G PTGR2,AC005520.3 Ensembl:ENSG00000140043,Ensembl:ENSG00000258653 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs994578820 Functional Loss SNV dbSNP153 33..33 33 - - - 16735 RMVar_ID_16735 Human_SNP_ID_560629603 A-to-I Human chr14 + 73862745 73862745 73862745 TTAATTTTTAACTTTTTTGAAATGAGATCTCTATTGCTGAGGCTGAGTGCAGTGGTGTGAATACA TTAATTTTTAACTTTTTTGAAATGAGATCTCTGTTGCTGAGGCTGAGTGCAGTGGTGTGAATACA A G PTGR2,AC005520.3 Ensembl:ENSG00000140043,Ensembl:ENSG00000258653 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs565909926 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12415820 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_167811,RMVar_hsa_circ_61290,RMVar_hsa_circ_167812,RMVar_hsa_circ_167810 16736 RMVar_ID_16736 Human_SNP_ID_560630106 A-to-I Human chr14 + 73865154 73865154 73865154 TGGAAGCTGAGAGTTCCCATGATAGGCTGTCTACAAACTGGAGAACCAGAGAAGCTGGTAGCATG TGGAAGCTGAGAGTTCCCATGATAGGCTGTCTGCAAACTGGAGAACCAGAGAAGCTGGTAGCATG A G PTGR2,AC005520.3 Ensembl:ENSG00000140043,Ensembl:ENSG00000258653 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1234658422 Functional Loss SNV dbSNP153 33..33 33 - - - 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_167811,RMVar_hsa_circ_61290,RMVar_hsa_circ_167812,RMVar_hsa_circ_167810 16737 RMVar_ID_16737 Human_SNP_ID_560638848 A-to-I Human chr14 + 73900018 73900018 73900018 AGGAATTCGAGACCAGCCTGACCAACGTGGAGAAATCCCGTCTCTACTAAAAATACAAAATTAGC AGGAATTCGAGACCAGCCTGACCAACGTGGAGGAATCCCGTCTCTACTAAAAATACAAAATTAGC A G ZNF410,AC005520.3 Ensembl:ENSG00000119725,Ensembl:ENSG00000258653 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1411024594 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101082,RMVar_hsa_circ_84235,RMVar_hsa_circ_167811,RMVar_hsa_circ_167812,RMVar_hsa_circ_72779,RMVar_hsa_circ_167816,RMVar_hsa_circ_167815,RMVar_hsa_circ_83272,RMVar_hsa_circ_325425,RMVar_hsa_circ_316748,RMVar_hsa_circ_276658,RMVar_hsa_circ_167817,RMVar_hsa_circ_315487,RMVar_hsa_circ_349855,RMVar_hsa_circ_351316,RMVar_hsa_circ_298339,RMVar_hsa_circ_167821,RMVar_hsa_circ_167822,RMVar_hsa_circ_302014,RMVar_hsa_circ_365636,RMVar_hsa_circ_39439,RMVar_hsa_circ_167823,RMVar_hsa_circ_296248 16738 RMVar_ID_16738 Human_SNP_ID_560638855 A-to-I Human chr14 + 73900031 73900031 73900031 CAGCCTGACCAACGTGGAGAAATCCCGTCTCTACTAAAAATACAAAATTAGCTGGGCGTGGTGGC CAGCCTGACCAACGTGGAGAAATCCCGTCTCTCCTAAAAATACAAAATTAGCTGGGCGTGGTGGC A C ZNF410,AC005520.3 Ensembl:ENSG00000119725,Ensembl:ENSG00000258653 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs974441220 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101082,RMVar_hsa_circ_84235,RMVar_hsa_circ_167811,RMVar_hsa_circ_167812,RMVar_hsa_circ_72779,RMVar_hsa_circ_167816,RMVar_hsa_circ_167815,RMVar_hsa_circ_83272,RMVar_hsa_circ_325425,RMVar_hsa_circ_316748,RMVar_hsa_circ_276658,RMVar_hsa_circ_167817,RMVar_hsa_circ_315487,RMVar_hsa_circ_349855,RMVar_hsa_circ_351316,RMVar_hsa_circ_298339,RMVar_hsa_circ_167821,RMVar_hsa_circ_167822,RMVar_hsa_circ_302014,RMVar_hsa_circ_365636,RMVar_hsa_circ_39439,RMVar_hsa_circ_167823,RMVar_hsa_circ_296248 16739 RMVar_ID_16739 Human_SNP_ID_560638858 A-to-I Human chr14 + 73900040 73900040 73900040 CAACGTGGAGAAATCCCGTCTCTACTAAAAATACAAAATTAGCTGGGCGTGGTGGCGCATGCATG CAACGTGGAGAAATCCCGTCTCTACTAAAAATTCAAAATTAGCTGGGCGTGGTGGCGCATGCATG A T ZNF410,AC005520.3 Ensembl:ENSG00000119725,Ensembl:ENSG00000258653 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1002227960 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101082,RMVar_hsa_circ_84235,RMVar_hsa_circ_167811,RMVar_hsa_circ_167812,RMVar_hsa_circ_72779,RMVar_hsa_circ_167816,RMVar_hsa_circ_167815,RMVar_hsa_circ_83272,RMVar_hsa_circ_325425,RMVar_hsa_circ_316748,RMVar_hsa_circ_276658,RMVar_hsa_circ_167817,RMVar_hsa_circ_315487,RMVar_hsa_circ_349855,RMVar_hsa_circ_351316,RMVar_hsa_circ_298339,RMVar_hsa_circ_167821,RMVar_hsa_circ_167822,RMVar_hsa_circ_302014,RMVar_hsa_circ_365636,RMVar_hsa_circ_39439,RMVar_hsa_circ_167823,RMVar_hsa_circ_296248 16740 RMVar_ID_16740 Human_SNP_ID_560638978 A-to-I Human chr14 + 73900491 73900491 73900491 CTGCCTCCTGGGCTCAAGTGATTCTCTGCCTCAGCCTCCCGAGTAGCTGGGACTACATGTGCATG CTGCCTCCTGGGCTCAAGTGATTCTCTGCCTCGGCCTCCCGAGTAGCTGGGACTACATGTGCATG A G ZNF410,AC005520.3 Ensembl:ENSG00000119725,Ensembl:ENSG00000258653 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs752250547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12416090 RMVar_hsa_circ_101082,RMVar_hsa_circ_84235,RMVar_hsa_circ_167811,RMVar_hsa_circ_167812,RMVar_hsa_circ_72779,RMVar_hsa_circ_167816,RMVar_hsa_circ_167815,RMVar_hsa_circ_83272,RMVar_hsa_circ_325425,RMVar_hsa_circ_316748,RMVar_hsa_circ_276658,RMVar_hsa_circ_167817,RMVar_hsa_circ_315487,RMVar_hsa_circ_349855,RMVar_hsa_circ_351316,RMVar_hsa_circ_298339,RMVar_hsa_circ_167821,RMVar_hsa_circ_167822,RMVar_hsa_circ_302014,RMVar_hsa_circ_365636,RMVar_hsa_circ_39439,RMVar_hsa_circ_167823,RMVar_hsa_circ_296248 16741 RMVar_ID_16741 Human_SNP_ID_560639342 A-to-I Human chr14 + 73901879 73901879 73901879 TCTCCTGAGTTGGGGAGGTCGAGGCTGCAGTGAACCGAGATCATGCCACTGGATTCCAGCCTGGG TCTCCTGAGTTGGGGAGGTCGAGGCTGCAGTGGACCGAGATCATGCCACTGGATTCCAGCCTGGG A G ZNF410,AC005520.3 Ensembl:ENSG00000119725,Ensembl:ENSG00000258653 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs866644651 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101082,RMVar_hsa_circ_84235,RMVar_hsa_circ_167811,RMVar_hsa_circ_167812,RMVar_hsa_circ_72779,RMVar_hsa_circ_167816,RMVar_hsa_circ_167815,RMVar_hsa_circ_83272,RMVar_hsa_circ_325425,RMVar_hsa_circ_316748,RMVar_hsa_circ_276658,RMVar_hsa_circ_167817,RMVar_hsa_circ_315487,RMVar_hsa_circ_349855,RMVar_hsa_circ_351316,RMVar_hsa_circ_298339,RMVar_hsa_circ_167821,RMVar_hsa_circ_167822,RMVar_hsa_circ_302014,RMVar_hsa_circ_365636,RMVar_hsa_circ_39439,RMVar_hsa_circ_167823,RMVar_hsa_circ_296248 16742 RMVar_ID_16742 Human_SNP_ID_560642619 A-to-I Human chr14 + 73914728 73914728 73914728 TGGGCTCACTGCAGCCTCTGCCTCCCGGGTTCAAGAGATTCTATTGCCTCAGCCTCCTGAGAAGC TGGGCTCACTGCAGCCTCTGCCTCCCGGGTTCGAGAGATTCTATTGCCTCAGCCTCCTGAGAAGC A G ZNF410,AC005520.3 Ensembl:ENSG00000119725,Ensembl:ENSG00000258653 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs987143427 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12416336 RMVar_hsa_circ_167815,RMVar_hsa_circ_83272,RMVar_hsa_circ_316748,RMVar_hsa_circ_29919,RMVar_hsa_circ_349855,RMVar_hsa_circ_39439,RMVar_hsa_circ_373197,RMVar_hsa_circ_167825,RMVar_hsa_circ_36365,RMVar_hsa_circ_167827,RMVar_hsa_circ_345392 16743 RMVar_ID_16743 Human_SNP_ID_560642796 A-to-I Human chr14 + 73915437 73915437 73915437 TTGGCTCACTGCAACCTCTGCCTCCTGAGTTCAAGCGATTCTCCTGCCTCAGCCTTCCGAGTAGT TTGGCTCACTGCAACCTCTGCCTCCTGAGTTCCAGCGATTCTCCTGCCTCAGCCTTCCGAGTAGT A C ZNF410,AC005520.3 Ensembl:ENSG00000119725,Ensembl:ENSG00000258653 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs951127356 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167815,RMVar_hsa_circ_83272,RMVar_hsa_circ_316748,RMVar_hsa_circ_29919,RMVar_hsa_circ_349855,RMVar_hsa_circ_39439,RMVar_hsa_circ_373197,RMVar_hsa_circ_167825,RMVar_hsa_circ_36365,RMVar_hsa_circ_167827,RMVar_hsa_circ_345392 16744 RMVar_ID_16744 Human_SNP_ID_560642831 A-to-I Human chr14 + 73915591 73915591 73915591 GAACTTCTGACCTGAAATGATCCACCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG GAACTTCTGACCTGAAATGATCCACCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG A G ZNF410,AC005520.3 Ensembl:ENSG00000119725,Ensembl:ENSG00000258653 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1302259088 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12416342 RMVar_hsa_circ_167815,RMVar_hsa_circ_83272,RMVar_hsa_circ_316748,RMVar_hsa_circ_29919,RMVar_hsa_circ_349855,RMVar_hsa_circ_39439,RMVar_hsa_circ_373197,RMVar_hsa_circ_167825,RMVar_hsa_circ_36365,RMVar_hsa_circ_167827,RMVar_hsa_circ_345392 16745 RMVar_ID_16745 Human_SNP_ID_560643132 A-to-I Human chr14 + 73916870 73916870 73916870 GGGTGTGGTGGCATACACCTGTAATCCCAGCTACTTGAAAGGCTGAGGCATGAGGATCTCTCGAA GGGTGTGGTGGCATACACCTGTAATCCCAGCTGCTTGAAAGGCTGAGGCATGAGGATCTCTCGAA A G ZNF410,AC005520.3 Ensembl:ENSG00000119725,Ensembl:ENSG00000258653 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1206777027 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167815,RMVar_hsa_circ_83272,RMVar_hsa_circ_316748,RMVar_hsa_circ_29919,RMVar_hsa_circ_349855,RMVar_hsa_circ_39439,RMVar_hsa_circ_373197,RMVar_hsa_circ_167825,RMVar_hsa_circ_36365,RMVar_hsa_circ_167827,RMVar_hsa_circ_345392 16746 RMVar_ID_16746 Human_SNP_ID_560645233 A-to-I Human chr14 + 73925531 73925531 73925531 CTCACTGCAACCTCCGCCTCTCAGGTTCAAGCAATTTTCCTGCCTCAGTCTCCTGAATAGCTGGG CTCACTGCAACCTCCGCCTCTCAGGTTCAAGCGATTTTCCTGCCTCAGTCTCCTGAATAGCTGGG A G ZNF410,AC005520.3 Ensembl:ENSG00000119725,Ensembl:ENSG00000258653 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1385137455 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167815,RMVar_hsa_circ_83272 16747 RMVar_ID_16747 Human_SNP_ID_560645249 A-to-I Human chr14 + 73925593 73925593 73925593 GGGATTGCAGGCACCCACTACCAAACCCGGCTAATTTTTGTATTTTTATTAGAGATAGGGTTTTA GGGATTGCAGGCACCCACTACCAAACCCGGCTGATTTTTGTATTTTTATTAGAGATAGGGTTTTA A G ZNF410,AC005520.3 Ensembl:ENSG00000119725,Ensembl:ENSG00000258653 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1284235499 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167815,RMVar_hsa_circ_83272 16748 RMVar_ID_16748 Human_SNP_ID_560645300 A-to-I Human chr14 + 73925830 73925830 73925830 GAGGCAAGTGGATTGCTTGAATCCAGGAGTTCAAGACCAGCCTGGGCAACATAAGACCCCTATCT GAGGCAAGTGGATTGCTTGAATCCAGGAGTTCGAGACCAGCCTGGGCAACATAAGACCCCTATCT A G ZNF410,AC005520.3 Ensembl:ENSG00000119725,Ensembl:ENSG00000258653 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1211822974 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167815,RMVar_hsa_circ_83272 16749 RMVar_ID_16749 Human_SNP_ID_560646463 A-to-I Human chr14 + 73930736 73930736 73930736 GTGATCCTCCTCCCTCAGCCTCCCAAGTAGCTAGGACTGCAAGCATGTACCACCATGCTTAATTT GTGATCCTCCTCCCTCAGCCTCCCAAGTAGCTGGGACTGCAAGCATGTACCACCATGCTTAATTT A G ZNF410,AC005520.3 Ensembl:ENSG00000119725,Ensembl:ENSG00000258653 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs370647987 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167815,RMVar_hsa_circ_83272 16750 RMVar_ID_16750 Human_SNP_ID_560646477 A-to-I Human chr14 + 73930784 73930784 73930784 ACCACCATGCTTAATTTTTAAAATTTTCTTGTAGAGACAGGGCCTCACTGTGTTGCCCAAGTGGG ACCACCATGCTTAATTTTTAAAATTTTCTTGTGGAGACAGGGCCTCACTGTGTTGCCCAAGTGGG A G ZNF410,AC005520.3 Ensembl:ENSG00000119725,Ensembl:ENSG00000258653 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1311647648 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167815,RMVar_hsa_circ_83272 16751 RMVar_ID_16751 Human_SNP_ID_560652514 A-to-I Human chr14 + 73953310 73953310 73953310 ATATGTTATTGCTTAGGACTCTGCATGGGTATAGTGTTTATGTTCTCTGTAAGAAATTCATATTC ATATGTTATTGCTTAGGACTCTGCATGGGTATGGTGTTTATGTTCTCTGTAAGAAATTCATATTC A G COQ6 Ensembl:ENSG00000119723 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1169564227 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18656284 RMVar_hsa_circ_167830,RMVar_hsa_circ_100411 16752 RMVar_ID_16752 Human_SNP_ID_560653844 A-to-I Human chr14 + 73957698 73957698 73957698 GTGATCCTCCTGCCTCAGCCTCCCTAAGTTCTAGGATTACGAGCATGAGCCACCCGTGCCTGGCC GTGATCCTCCTGCCTCAGCCTCCCTAAGTTCTGGGATTACGAGCATGAGCCACCCGTGCCTGGCC A G COQ6 Ensembl:ENSG00000119723 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,frontal_cortex - 29129909,30559470 RNA-Seq:(High) rs1292873264 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12416700 RMVar_hsa_circ_87374,RMVar_hsa_circ_73200,RMVar_hsa_circ_41438,RMVar_hsa_circ_167832,RMVar_hsa_circ_119333,RMVar_hsa_circ_167834 16753 RMVar_ID_16753 Human_SNP_ID_560662299 A-to-I Human chr14 - 73989973 73989973 73989973 AGACGAAGTCTTGCTCTGTTGCCCAAGCTGGAATGTAGTGGGGCGATGTCTGCTCACTGGAACCT AGACGAAGTCTTGCTCTGTTGCCCAAGCTGGATTGTAGTGGGGCGATGTCTGCTCACTGGAACCT T A ENTPD5 Ensembl:ENSG00000187097 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879141072 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167842,RMVar_hsa_circ_109289,RMVar_hsa_circ_358420,RMVar_hsa_circ_167838,RMVar_hsa_circ_360217,RMVar_hsa_circ_356669,RMVar_hsa_circ_70182,RMVar_hsa_circ_353458,RMVar_hsa_circ_111833,RMVar_hsa_circ_356444 16754 RMVar_ID_16754 Human_SNP_ID_560662300 A-to-I Human chr14 - 73989973 73989973 73989973 AGACGAAGTCTTGCTCTGTTGCCCAAGCTGGAATGTAGTGGGGCGATGTCTGCTCACTGGAACCT AGACGAAGTCTTGCTCTGTTGCCCAAGCTGGAGTGTAGTGGGGCGATGTCTGCTCACTGGAACCT T C ENTPD5 Ensembl:ENSG00000187097 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879141072 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167842,RMVar_hsa_circ_109289,RMVar_hsa_circ_358420,RMVar_hsa_circ_167838,RMVar_hsa_circ_360217,RMVar_hsa_circ_356669,RMVar_hsa_circ_70182,RMVar_hsa_circ_353458,RMVar_hsa_circ_111833,RMVar_hsa_circ_356444 16755 RMVar_ID_16755 Human_SNP_ID_560664124 A-to-I Human chr14 - 73996726 73996726 73996726 TTGCCCAAGGTGGTCTTGAAATCCTGACCTCAAGTAATCCTCCTGCCTCGACCTTCCAAAGTGCT TTGCCCAAGGTGGTCTTGAAATCCTGACCTCAGGTAATCCTCCTGCCTCGACCTTCCAAAGTGCT T C ENTPD5 Ensembl:ENSG00000187097 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1189812995 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1534954 RMVar_hsa_circ_167842,RMVar_hsa_circ_109289,RMVar_hsa_circ_358420,RMVar_hsa_circ_167838,RMVar_hsa_circ_360217,RMVar_hsa_circ_356669,RMVar_hsa_circ_70182,RMVar_hsa_circ_353458,RMVar_hsa_circ_111833,RMVar_hsa_circ_356444 16756 RMVar_ID_16756 Human_SNP_ID_560664684 A-to-I Human chr14 - 73999277 73999277 73999277 CACCACGTTGGCCAGGCTGGTCACGAACTCCTAACTTGAGGTAATCCACCCACTTTGGCCTCCCA CACCACGTTGGCCAGGCTGGTCACGAACTCCTGACTTGAGGTAATCCACCCACTTTGGCCTCCCA T C ENTPD5 Ensembl:ENSG00000187097 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1247597855 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167842,RMVar_hsa_circ_109289,RMVar_hsa_circ_358420,RMVar_hsa_circ_167838,RMVar_hsa_circ_360217,RMVar_hsa_circ_356669,RMVar_hsa_circ_70182,RMVar_hsa_circ_353458,RMVar_hsa_circ_111833,RMVar_hsa_circ_356444 16757 RMVar_ID_16757 Human_SNP_ID_560666073 A-to-I Human chr14 - 74004435 74004435 74004435 AGATAGGCCGGGCGCAATGGCTCACACCTGTAATCTCAGCACTTTGGGAGGCCAACGCAGGTGGA AGATAGGCCGGGCGCAATGGCTCACACCTGTATTCTCAGCACTTTGGGAGGCCAACGCAGGTGGA T A ENTPD5 Ensembl:ENSG00000187097 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs573319660 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6383446 RMVar_hsa_circ_167842,RMVar_hsa_circ_109289,RMVar_hsa_circ_358420,RMVar_hsa_circ_167838,RMVar_hsa_circ_360217,RMVar_hsa_circ_356669,RMVar_hsa_circ_70182,RMVar_hsa_circ_353458,RMVar_hsa_circ_111833,RMVar_hsa_circ_356444 16758 RMVar_ID_16758 Human_SNP_ID_560666074 A-to-I Human chr14 - 74004435 74004435 74004435 AGATAGGCCGGGCGCAATGGCTCACACCTGTAATCTCAGCACTTTGGGAGGCCAACGCAGGTGGA AGATAGGCCGGGCGCAATGGCTCACACCTGTAGTCTCAGCACTTTGGGAGGCCAACGCAGGTGGA T C ENTPD5 Ensembl:ENSG00000187097 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs573319660 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6383446 RMVar_hsa_circ_167842,RMVar_hsa_circ_109289,RMVar_hsa_circ_358420,RMVar_hsa_circ_167838,RMVar_hsa_circ_360217,RMVar_hsa_circ_356669,RMVar_hsa_circ_70182,RMVar_hsa_circ_353458,RMVar_hsa_circ_111833,RMVar_hsa_circ_356444 16759 RMVar_ID_16759 Human_SNP_ID_560666075 A-to-I Human chr14 - 74004442 74004442 74004442 AATAATGAGATAGGCCGGGCGCAATGGCTCACACCTGTAATCTCAGCACTTTGGGAGGCCAACGC AATAATGAGATAGGCCGGGCGCAATGGCTCACGCCTGTAATCTCAGCACTTTGGGAGGCCAACGC T C ENTPD5 Ensembl:ENSG00000187097 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1187476415 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6383446 RMVar_hsa_circ_167842,RMVar_hsa_circ_109289,RMVar_hsa_circ_358420,RMVar_hsa_circ_167838,RMVar_hsa_circ_360217,RMVar_hsa_circ_356669,RMVar_hsa_circ_70182,RMVar_hsa_circ_353458,RMVar_hsa_circ_111833,RMVar_hsa_circ_356444 16760 RMVar_ID_16760 Human_SNP_ID_560666405 A-to-I Human chr14 - 74005413 74005413 74005413 GAGGATTGCTTGAGGCCAGGAGTTTGAGAGCAATCTGACAAACATAGTGAAACCCTGCCTATATT GAGGATTGCTTGAGGCCAGGAGTTTGAGAGCAGTCTGACAAACATAGTGAAACCCTGCCTATATT T C ENTPD5 Ensembl:ENSG00000187097 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1226636063 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167842,RMVar_hsa_circ_109289,RMVar_hsa_circ_358420,RMVar_hsa_circ_167838,RMVar_hsa_circ_360217,RMVar_hsa_circ_356669,RMVar_hsa_circ_70182,RMVar_hsa_circ_353458,RMVar_hsa_circ_111833,RMVar_hsa_circ_356444,RMVar_hsa_circ_296110,RMVar_hsa_circ_349578 16761 RMVar_ID_16761 Human_SNP_ID_560668928 A-to-I Human chr14 - 74015586 74015586 74015586 CACTTTGGGAGGCCAAGGCAGACGGATTGCTTAAGCCCAGGAGTTCAAGACCAGTCTGGACAACA CACTTTGGGAGGCCAAGGCAGACGGATTGCTTGAGCCCAGGAGTTCAAGACCAGTCTGGACAACA T C ENTPD5 Ensembl:ENSG00000187097 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264243571 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167842,RMVar_hsa_circ_358420,RMVar_hsa_circ_360217,RMVar_hsa_circ_356669,RMVar_hsa_circ_70182,RMVar_hsa_circ_111833,RMVar_hsa_circ_349578,RMVar_hsa_circ_363946 16762 RMVar_ID_16762 Human_SNP_ID_560676889 A-to-I Human chr14 + 74046447 74046447 74046447 CAGGCTGGAGTGCAGCGGCATGAGCTTGGCTCACTGCAACCTCTGCCTCCCGAGTTCAGGCGATT CAGGCTGGAGTGCAGCGGCATGAGCTTGGCTCCCTGCAACCTCTGCCTCCCGAGTTCAGGCGATT A C BBOF1 Ensembl:ENSG00000119636 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1436181272 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73664,RMVar_hsa_circ_310095,RMVar_hsa_circ_63684,RMVar_hsa_circ_167844,RMVar_hsa_circ_167845,RMVar_hsa_circ_363488,RMVar_hsa_circ_35435 16763 RMVar_ID_16763 Human_SNP_ID_560677463 A-to-I Human chr14 + 74049012 74049012 74049012 CTCCTGACCCAGCCTCCTGAGTAGCTGGGACTACAGGCATGCACCACCACGGCCAGCTAATTTTT CTCCTGACCCAGCCTCCTGAGTAGCTGGGACTGCAGGCATGCACCACCACGGCCAGCTAATTTTT A G BBOF1 Ensembl:ENSG00000119636 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1387962006 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73664,RMVar_hsa_circ_310095,RMVar_hsa_circ_63684,RMVar_hsa_circ_167844,RMVar_hsa_circ_167845,RMVar_hsa_circ_363488,RMVar_hsa_circ_35435,RMVar_hsa_circ_29822 16764 RMVar_ID_16764 Human_SNP_ID_560679782 A-to-I Human chr14 - 74058187 74058174 74058187 GAGTAGCTGGGATTACAGGTGCATGCCCCCACACCCGGATAATTTTTTGTACTTTTAGTAGAGAC GAGTAGCTGGGATTACAGGTGCATGCCCCCAC_____________TTTGTACTTTTAGTAGAGAC AAAATTATCCGGGT A ALDH6A1 Ensembl:ENSG00000119711 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs963027933 Functional Loss DEL dbSNP153 33..45 33 - - - 16765 RMVar_ID_16765 Human_SNP_ID_560679940 A-to-I Human chr14 - 74058840 74058840 74058840 CCTCAGGTGATCTGCCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCACCCC CCTCAGGTGATCTGCCTGCCTTGGCCTCCCAAGGTGCTGGGATTACAGGTGTGAGCCACCACCCC T C ALDH6A1 Ensembl:ENSG00000119711 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1128353 Functional Loss SNV dbSNP153 33..33 33 - - - 16766 RMVar_ID_16766 Human_SNP_ID_560680089 A-to-I Human chr14 - 74059421 74059421 74059421 AAAGTGCTGGGATTACAGGCATGAGCCACCACACCCAGCCAGATGCAAATAATTTTCTTAGAAAA AAAGTGCTGGGATTACAGGCATGAGCCACCACGCCCAGCCAGATGCAAATAATTTTCTTAGAAAA T C ALDH6A1 Ensembl:ENSG00000119711 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1488222384 Functional Loss SNV dbSNP153 33..33 33 - - - 16767 RMVar_ID_16767 Human_SNP_ID_560680274 A-to-I Human chr14 - 74060242 74060242 74060242 TAATTCCATCATTTTGGGAGGCCACAGTGGGCAGATTGCTTGAGCCCAGGAGTTGAAGAACGTGG TAATTCCATCATTTTGGGAGGCCACAGTGGGCGGATTGCTTGAGCCCAGGAGTTGAAGAACGTGG T C ALDH6A1 Ensembl:ENSG00000119711 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1135884 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26431704 16768 RMVar_ID_16768 Human_SNP_ID_560680282 A-to-I Human chr14 - 74060272 74060272 74060272 GTTCCAGCCAGGCGCGGTGGCTCACGCCTGTAATTCCATCATTTTGGGAGGCCACAGTGGGCAGA GTTCCAGCCAGGCGCGGTGGCTCACGCCTGTAGTTCCATCATTTTGGGAGGCCACAGTGGGCAGA T C ALDH6A1 Ensembl:ENSG00000119711 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1135883 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26431704 16769 RMVar_ID_16769 Human_SNP_ID_560680283 A-to-I Human chr14 - 74060273 74060273 74060273 TGTTCCAGCCAGGCGCGGTGGCTCACGCCTGTAATTCCATCATTTTGGGAGGCCACAGTGGGCAG TGTTCCAGCCAGGCGCGGTGGCTCACGCCTGTGATTCCATCATTTTGGGAGGCCACAGTGGGCAG T C ALDH6A1 Ensembl:ENSG00000119711 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1135882 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26431704 16770 RMVar_ID_16770 Human_SNP_ID_560680286 A-to-I Human chr14 - 74060281 74060281 74060281 AAAGAAAATGTTCCAGCCAGGCGCGGTGGCTCACGCCTGTAATTCCATCATTTTGGGAGGCCACA AAAGAAAATGTTCCAGCCAGGCGCGGTGGCTCCCGCCTGTAATTCCATCATTTTGGGAGGCCACA T G ALDH6A1 Ensembl:ENSG00000119711 Protein coding 3'UTR GSE38233;GSE99789;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29796672,32596459 RNA-Seq:(High) rs1278255831 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26431704 16771 RMVar_ID_16771 Human_SNP_ID_560685185 A-to-I Human chr14 - 74080716 74080716 74080716 AGAGTAGGCTGGGTGTGATGGCTCATGCCTGTAATCCCAACACTTTGGGTGGCCCAGGCAGGAGG AGAGTAGGCTGGGTGTGATGGCTCATGCCTGTTATCCCAACACTTTGGGTGGCCCAGGCAGGAGG T A ALDH6A1 Ensembl:ENSG00000119711 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs920191984 Functional Loss SNV dbSNP153 33..33 33 - - - 16772 RMVar_ID_16772 Human_SNP_ID_560686939 A-to-I Human chr14 + 74088012 74088012 74088012 ATGATTATAGCTCACTGCACCCTCAAAGGCTCAAGCGATTCTCCCATCTCAGCCTCCTAAGTAGC ATGATTATAGCTCACTGCACCCTCAAAGGCTCGAGCGATTCTCCCATCTCAGCCTCCTAAGTAGC A G LIN52 Ensembl:ENSG00000205659 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1294496539 Functional Loss SNV dbSNP153 33..33 33 - - - 16773 RMVar_ID_16773 Human_SNP_ID_560687010 A-to-I Human chr14 + 74088305 74088305 74088305 TAGAGACGGGGTTTCACCATGTTGCCCAGGCTAGTCTTGAACTCCTGACCTCAGGTGATGCACTC TAGAGACGGGGTTTCACCATGTTGCCCAGGCTGGTCTTGAACTCCTGACCTCAGGTGATGCACTC A G LIN52 Ensembl:ENSG00000205659 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1181911818 Functional Loss SNV dbSNP153 33..33 33 - - - 16774 RMVar_ID_16774 Human_SNP_ID_560687020 A-to-I Human chr14 + 74088352 74088352 74088352 ACCTCAGGTGATGCACTCACCTCGGCCTCCCAAAGTGCTAGGATTACAGGCGTGAGCCACCATGC ACCTCAGGTGATGCACTCACCTCGGCCTCCCAGAGTGCTAGGATTACAGGCGTGAGCCACCATGC A G LIN52 Ensembl:ENSG00000205659 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1317706816 Functional Loss SNV dbSNP153 33..33 33 - - - 16775 RMVar_ID_16775 Human_SNP_ID_560687022 A-to-I Human chr14 + 74088359 74088359 74088359 GTGATGCACTCACCTCGGCCTCCCAAAGTGCTAGGATTACAGGCGTGAGCCACCATGCCCCCACC GTGATGCACTCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCATGCCCCCACC A G LIN52 Ensembl:ENSG00000205659 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs895410600 Functional Loss SNV dbSNP153 33..33 33 - - - 16776 RMVar_ID_16776 Human_SNP_ID_560687033 A-to-I Human chr14 + 74088406 74088406 74088406 AGCCACCATGCCCCCACCTTATTATTTTTTGTAGAGATGGAGTCTCACTATGTTGCCCAGGATGG AGCCACCATGCCCCCACCTTATTATTTTTTGTGGAGATGGAGTCTCACTATGTTGCCCAGGATGG A G LIN52 Ensembl:ENSG00000205659 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1057467902 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12417031 16777 RMVar_ID_16777 Human_SNP_ID_560687302 A-to-I Human chr14 + 74089568 74089568 74089568 TTTTTTGCTTTTTGTAGAGATGGGTTTTCACTATGTTGGCCAGGCTGGTCTCAAACTCGTGAGCT TTTTTTGCTTTTTGTAGAGATGGGTTTTCACTCTGTTGGCCAGGCTGGTCTCAAACTCGTGAGCT A C LIN52 Ensembl:ENSG00000205659 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs899934526 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12417096 16778 RMVar_ID_16778 Human_SNP_ID_560687303 A-to-I Human chr14 + 74089568 74089568 74089568 TTTTTTGCTTTTTGTAGAGATGGGTTTTCACTATGTTGGCCAGGCTGGTCTCAAACTCGTGAGCT TTTTTTGCTTTTTGTAGAGATGGGTTTTCACTGTGTTGGCCAGGCTGGTCTCAAACTCGTGAGCT A G LIN52 Ensembl:ENSG00000205659 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs899934526 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12417096 16779 RMVar_ID_16779 Human_SNP_ID_560688167 A-to-I Human chr14 + 74093051 74093051 74093051 TCGGCTCACTGCAACGTCCGCCTCCCTGGTTCAAGCGATGCTCCTGCCTCAGCCTCCCGAGTAGC TCGGCTCACTGCAACGTCCGCCTCCCTGGTTCTAGCGATGCTCCTGCCTCAGCCTCCCGAGTAGC A T LIN52 Ensembl:ENSG00000205659 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1478041612 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167853,RMVar_hsa_circ_278473,RMVar_hsa_circ_344177,RMVar_hsa_circ_167852 16780 RMVar_ID_16780 Human_SNP_ID_560688284 A-to-I Human chr14 + 74093504 74093504 74093504 CATGCCACCACACCTGGCTAATTTTTGTATTTATAGTAGAGAAGAGGCTTCACCATGTTGGACAG CATGCCACCACACCTGGCTAATTTTTGTATTTGTAGTAGAGAAGAGGCTTCACCATGTTGGACAG A G LIN52 Ensembl:ENSG00000205659 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs8003415 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_63 GWAS_ID_1201,GWAS_ID_1202,GWAS_ID_1203,GWAS_ID_1204,GWAS_ID_1205,GWAS_ID_1206,GWAS_ID_1207,GWAS_ID_1208 RMVar_hsa_circ_167853,RMVar_hsa_circ_278473,RMVar_hsa_circ_344177,RMVar_hsa_circ_167852 16781 RMVar_ID_16781 Human_SNP_ID_560688285 A-to-I Human chr14 + 74093504 74093504 74093504 CATGCCACCACACCTGGCTAATTTTTGTATTTATAGTAGAGAAGAGGCTTCACCATGTTGGACAG CATGCCACCACACCTGGCTAATTTTTGTATTTTTAGTAGAGAAGAGGCTTCACCATGTTGGACAG A T LIN52 Ensembl:ENSG00000205659 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs8003415 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_63 GWAS_ID_1201,GWAS_ID_1202,GWAS_ID_1203,GWAS_ID_1204,GWAS_ID_1205,GWAS_ID_1206,GWAS_ID_1207,GWAS_ID_1208 RMVar_hsa_circ_167853,RMVar_hsa_circ_278473,RMVar_hsa_circ_344177,RMVar_hsa_circ_167852 16782 RMVar_ID_16782 Human_SNP_ID_560688299 A-to-I Human chr14 + 74093562 74093562 74093562 TGGACAGGCTGGTCTTGAACTCCAGACCTCAGATGATCTGCCTGCCTCAGCCTCCCAAAGTGCTA TGGACAGGCTGGTCTTGAACTCCAGACCTCAGGTGATCTGCCTGCCTCAGCCTCCCAAAGTGCTA A G LIN52 Ensembl:ENSG00000205659 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1464341125 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167853,RMVar_hsa_circ_278473,RMVar_hsa_circ_344177,RMVar_hsa_circ_167852 16783 RMVar_ID_16783 Human_SNP_ID_560688350 A-to-I Human chr14 + 74093775 74093775 74093775 ATTACCTGAAGTCAGGAGTTTGAGATCAGCCTAGCTAACATGGCGAAACCCCGTTTCTACTAAAA ATTACCTGAAGTCAGGAGTTTGAGATCAGCCTGGCTAACATGGCGAAACCCCGTTTCTACTAAAA A G LIN52 Ensembl:ENSG00000205659 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs753279514 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167853,RMVar_hsa_circ_278473,RMVar_hsa_circ_344177,RMVar_hsa_circ_167852 16784 RMVar_ID_16784 Human_SNP_ID_560691093 A-to-I Human chr14 + 74104708 74104708 74104708 AGATTAATAGTTGATGGATTCTAGATCTAACTATCAGGAAATAAAAAGGGATAGGTGAACATGTT AGATTAATAGTTGATGGATTCTAGATCTAACTGTCAGGAAATAAAAAGGGATAGGTGAACATGTT A G LIN52 Ensembl:ENSG00000205659 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1198087455 Functional Loss SNV dbSNP153 33..33 33 - - - 16785 RMVar_ID_16785 Human_SNP_ID_560696493 A-to-I Human chr14 + 74129597 74129597 74129597 ACATGCAGCCGGGCACAGTGGCTCACACCTGTAATCCCAACACTCTGGGAGGCTGAGGCAGGAGG ACATGCAGCCGGGCACAGTGGCTCACACCTGTTATCCCAACACTCTGGGAGGCTGAGGCAGGAGG A T LIN52 Ensembl:ENSG00000205659 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1245287267 Functional Loss SNV dbSNP153 33..33 33 - - - 16786 RMVar_ID_16786 Human_SNP_ID_560696497 A-to-I Human chr14 + 74129624 74129624 74129624 CCTGTAATCCCAACACTCTGGGAGGCTGAGGCAGGAGGCTCACTTGAGCACAAGAGTTTGATATT CCTGTAATCCCAACACTCTGGGAGGCTGAGGCGGGAGGCTCACTTGAGCACAAGAGTTTGATATT A G LIN52 Ensembl:ENSG00000205659 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs999803069 Functional Loss SNV dbSNP153 33..33 33 - - - 16787 RMVar_ID_16787 Human_SNP_ID_560696526 A-to-I Human chr14 + 74129754 74129753 74129755 CCTGTAGTCACAGCTACTTGGGAGGCTGAGACAAGAGGATTCCTTGAATCCAGGAATTCGAGGCT CCTGTAGTCACAGCTACTTGGGAGGCTGAGAC__GAGGATTCCTTGAATCCAGGAATTCGAGGCT CAA C LIN52 Ensembl:ENSG00000205659 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946759421 Functional Loss DEL dbSNP153 33..34 33 - - - 16788 RMVar_ID_16788 Human_SNP_ID_560696527 A-to-I Human chr14 + 74129754 74129754 74129754 CCTGTAGTCACAGCTACTTGGGAGGCTGAGACAAGAGGATTCCTTGAATCCAGGAATTCGAGGCT CCTGTAGTCACAGCTACTTGGGAGGCTGAGACTAGAGGATTCCTTGAATCCAGGAATTCGAGGCT A T LIN52 Ensembl:ENSG00000205659 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1197265535 Functional Loss SNV dbSNP153 33..33 33 - - - 16789 RMVar_ID_16789 Human_SNP_ID_560705115 A-to-I Human chr14 + 74168765 74168765 74168765 ATCTAATACCTGAGTGAACTGGGTTACATGTTAAGAATTTCTGGACATAGGCCAGGTGTGGTGGC ATCTAATACCTGAGTGAACTGGGTTACATGTTGAGAATTTCTGGACATAGGCCAGGTGTGGTGGC A G LIN52 Ensembl:ENSG00000205659 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs555893617 Functional Loss SNV dbSNP153 33..33 33 - - - 16790 RMVar_ID_16790 Human_SNP_ID_560739037 A-to-I Human chr14 - 74298301 74298301 74298301 CGCCATTGCACTCCAGCCTGGGCAACAAGAGTAAAACTCCATCTCAGAGAAAAAAAATTTGGTGA CGCCATTGCACTCCAGCCTGGGCAACAAGAGTGAAACTCCATCTCAGAGAAAAAAAATTTGGTGA T C ABCD4 Ensembl:ENSG00000119688 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1004420655 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69013 16791 RMVar_ID_16791 Human_SNP_ID_560739461 A-to-I Human chr14 - 74299870 74299869 74299870 TTCAGTAAAGACAGGGTTTCACCATCTTGGCCAGGCTGATCTCGAACTCATGACCTCAGGTGATA TTCAGTAAAGACAGGGTTTCACCATCTTGGCC_GGCTGATCTCGAACTCATGACCTCAGGTGATA CT C ABCD4 Ensembl:ENSG00000119688 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs34430973 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_12419223 RMVar_hsa_circ_69013 16792 RMVar_ID_16792 Human_SNP_ID_560739463 A-to-I Human chr14 - 74299870 74299870 74299870 TTCAGTAAAGACAGGGTTTCACCATCTTGGCCAGGCTGATCTCGAACTCATGACCTCAGGTGATA TTCAGTAAAGACAGGGTTTCACCATCTTGGCCGGGCTGATCTCGAACTCATGACCTCAGGTGATA T C ABCD4 Ensembl:ENSG00000119688 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs997987461 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12419223 RMVar_hsa_circ_69013 16793 RMVar_ID_16793 Human_SNP_ID_560739701 A-to-I Human chr14 - 74300545 74300545 74300545 CTTGTTGCCCAGGCTCTTGTTGCAATGGCGCAATCTCAGCTCACTGCAACCTCTGCCTCCCAGGT CTTGTTGCCCAGGCTCTTGTTGCAATGGCGCAGTCTCAGCTCACTGCAACCTCTGCCTCCCAGGT T C ABCD4 Ensembl:ENSG00000119688 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1231694820 Functional Loss SNV dbSNP153 33..33 33 - - - 16794 RMVar_ID_16794 Human_SNP_ID_560740078 A-to-I Human chr14 - 74301818 74301818 74301818 CTCGGCTCACTGCAACCTCCGCCTCGGGTTCAAGCGATTCTTCTGCCTCAGCCTCCTGAGTAGCT CTCGGCTCACTGCAACCTCCGCCTCGGGTTCATGCGATTCTTCTGCCTCAGCCTCCTGAGTAGCT T A ABCD4 Ensembl:ENSG00000119688 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350217975 Functional Loss SNV dbSNP153 33..33 33 - - - 16795 RMVar_ID_16795 Human_SNP_ID_560784592 A-to-I Human chr14 + 74483106 74483106 74483106 TAGAAGATTCCTACAGAAAGCAAGTTGAAGTCAACTGCCAACAGTGTATGCTTAAAATCCTAGAT TAGAAGATTCCTACAGAAAGCAAGTTGAAGTCGACTGCCAACAGTGTATGCTTAAAATCCTAGAT A G RAP1AP Ensembl:ENSG00000258769 Pseudogene exon GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1200930170 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6402787 16796 RMVar_ID_16796 Human_SNP_ID_560784598 A-to-I Human chr14 + 74483135 74483135 74483135 GTCAACTGCCAACAGTGTATGCTTAAAATCCTAGATACTGCAGGCACAGGGCAATTTACAGCAAT GTCAACTGCCAACAGTGTATGCTTAAAATCCTGGATACTGCAGGCACAGGGCAATTTACAGCAAT A G RAP1AP Ensembl:ENSG00000258769 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202219442 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6402787 16797 RMVar_ID_16797 Human_SNP_ID_560784664 A-to-I Human chr14 + 74483454 74483453 74483454 ATATTTTATGACCTGGTCAGACAGATAAATAGAAAAACACCAGTGGAAAAGAAACAGCCTAAAAA ATATTTTATGACCTGGTCAGACAGATAAATAG_AAAACACCAGTGGAAAAGAAACAGCCTAAAAA GA G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1366774123 Functional Loss DEL dbSNP153 33..33 33 - - - 16798 RMVar_ID_16798 Human_SNP_ID_560784665 A-to-I Human chr14 + 74483454 74483454 74483454 ATATTTTATGACCTGGTCAGACAGATAAATAGAAAAACACCAGTGGAAAAGAAACAGCCTAAAAA ATATTTTATGACCTGGTCAGACAGATAAATAGCAAAACACCAGTGGAAAAGAAACAGCCTAAAAA A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878864008 Functional Loss SNV dbSNP153 33..33 33 - - - 16799 RMVar_ID_16799 Human_SNP_ID_560784666 A-to-I Human chr14 + 74483454 74483454 74483454 ATATTTTATGACCTGGTCAGACAGATAAATAGAAAAACACCAGTGGAAAAGAAACAGCCTAAAAA ATATTTTATGACCTGGTCAGACAGATAAATAGGAAAACACCAGTGGAAAAGAAACAGCCTAAAAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878864008 Functional Loss SNV dbSNP153 33..33 33 - - - 16800 RMVar_ID_16800 Human_SNP_ID_560788220 A-to-I Human chr14 + 74497466 74497466 74497466 CAATCTTCCCACCTCAGCCCCTGCAAGTAGCTAGGACTACAGGTGCACACCACCAAGCCCAGCTA CAATCTTCCCACCTCAGCCCCTGCAAGTAGCTGGGACTACAGGTGCACACCACCAAGCCCAGCTA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs952646898 Functional Loss SNV dbSNP153 33..33 33 - - - 16801 RMVar_ID_16801 Human_SNP_ID_560832375 A-to-I Human chr14 - 74677318 74677318 74677318 TAATTTTTATTTTTTGTAGAGATGGTCTTGCTATGTTGCTCAAGCTGGTCTTGAACTTCTTAAGG TAATTTTTATTTTTTGTAGAGATGGTCTTGCTCTGTTGCTCAAGCTGGTCTTGAACTTCTTAAGG T G AREL1 Ensembl:ENSG00000119682 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1451771508 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167933,RMVar_hsa_circ_50673,RMVar_hsa_circ_83554,RMVar_hsa_circ_167929,RMVar_hsa_circ_375725,RMVar_hsa_circ_41906,RMVar_hsa_circ_167934,RMVar_hsa_circ_369844,RMVar_hsa_circ_268868,RMVar_hsa_circ_373094,RMVar_hsa_circ_167935,RMVar_hsa_circ_357410,RMVar_hsa_circ_167938 16802 RMVar_ID_16802 Human_SNP_ID_560832386 A-to-I Human chr14 - 74677348 74677348 74677348 GGGACACAGGCATGAACCACCATGCCTGGCTAATTTTTATTTTTTGTAGAGATGGTCTTGCTATG GGGACACAGGCATGAACCACCATGCCTGGCTAGTTTTTATTTTTTGTAGAGATGGTCTTGCTATG T C AREL1 Ensembl:ENSG00000119682 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs902623001 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167933,RMVar_hsa_circ_50673,RMVar_hsa_circ_83554,RMVar_hsa_circ_167929,RMVar_hsa_circ_375725,RMVar_hsa_circ_41906,RMVar_hsa_circ_167934,RMVar_hsa_circ_369844,RMVar_hsa_circ_268868,RMVar_hsa_circ_373094,RMVar_hsa_circ_167935,RMVar_hsa_circ_357410,RMVar_hsa_circ_167938 16803 RMVar_ID_16803 Human_SNP_ID_560832387 A-to-I Human chr14 - 74677349 74677349 74677349 TGGGACACAGGCATGAACCACCATGCCTGGCTAATTTTTATTTTTTGTAGAGATGGTCTTGCTAT TGGGACACAGGCATGAACCACCATGCCTGGCTGATTTTTATTTTTTGTAGAGATGGTCTTGCTAT T C AREL1 Ensembl:ENSG00000119682 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1035016068 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167933,RMVar_hsa_circ_50673,RMVar_hsa_circ_83554,RMVar_hsa_circ_167929,RMVar_hsa_circ_375725,RMVar_hsa_circ_41906,RMVar_hsa_circ_167934,RMVar_hsa_circ_369844,RMVar_hsa_circ_268868,RMVar_hsa_circ_373094,RMVar_hsa_circ_167935,RMVar_hsa_circ_357410,RMVar_hsa_circ_167938 16804 RMVar_ID_16804 Human_SNP_ID_560833004 A-to-I Human chr14 - 74679661 74679661 74679661 ATCATGCCTGGCTAGTTTTTTGTGTTTTTAGTAGAGATGGGGTTTTGCCCTGTTAGACAGGCTGG ATCATGCCTGGCTAGTTTTTTGTGTTTTTAGTGGAGATGGGGTTTTGCCCTGTTAGACAGGCTGG T C AREL1 Ensembl:ENSG00000119682 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1366639274 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167933,RMVar_hsa_circ_50673,RMVar_hsa_circ_83554,RMVar_hsa_circ_167929,RMVar_hsa_circ_375725,RMVar_hsa_circ_41906,RMVar_hsa_circ_167934,RMVar_hsa_circ_369844,RMVar_hsa_circ_268868,RMVar_hsa_circ_373094,RMVar_hsa_circ_167935,RMVar_hsa_circ_357410,RMVar_hsa_circ_167938 16805 RMVar_ID_16805 Human_SNP_ID_560833096 A-to-I Human chr14 - 74680010 74680010 74680010 CACCACGCCTGGCTAATTTTTGTATATTTTGTAGAGACAGAGTTTTGCCATGTTGGCCAGGCAGG CACCACGCCTGGCTAATTTTTGTATATTTTGTGGAGACAGAGTTTTGCCATGTTGGCCAGGCAGG T C AREL1 Ensembl:ENSG00000119682 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1283570304 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12419726 RMVar_hsa_circ_167933,RMVar_hsa_circ_50673,RMVar_hsa_circ_83554,RMVar_hsa_circ_167929,RMVar_hsa_circ_375725,RMVar_hsa_circ_41906,RMVar_hsa_circ_167934,RMVar_hsa_circ_369844,RMVar_hsa_circ_268868,RMVar_hsa_circ_373094,RMVar_hsa_circ_167935,RMVar_hsa_circ_357410,RMVar_hsa_circ_167938 16806 RMVar_ID_16806 Human_SNP_ID_560833111 A-to-I Human chr14 - 74680076 74680076 74680076 CTCTTCCCAGGTTCTGGCAATTCTCCTGTGTCAGCCTCCTGAGTAGCTGGGATTACAGGCAGGCA CTCTTCCCAGGTTCTGGCAATTCTCCTGTGTCGGCCTCCTGAGTAGCTGGGATTACAGGCAGGCA T C AREL1 Ensembl:ENSG00000119682 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1026536324 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167933,RMVar_hsa_circ_50673,RMVar_hsa_circ_83554,RMVar_hsa_circ_167929,RMVar_hsa_circ_375725,RMVar_hsa_circ_41906,RMVar_hsa_circ_167934,RMVar_hsa_circ_369844,RMVar_hsa_circ_268868,RMVar_hsa_circ_373094,RMVar_hsa_circ_167935,RMVar_hsa_circ_357410,RMVar_hsa_circ_167938 16807 RMVar_ID_16807 Human_SNP_ID_560833114 A-to-I Human chr14 - 74680089 74680089 74680089 TGCAACCAACCTCCTCTTCCCAGGTTCTGGCAATTCTCCTGTGTCAGCCTCCTGAGTAGCTGGGA TGCAACCAACCTCCTCTTCCCAGGTTCTGGCAGTTCTCCTGTGTCAGCCTCCTGAGTAGCTGGGA T C AREL1 Ensembl:ENSG00000119682 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1359196222 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_167933,RMVar_hsa_circ_50673,RMVar_hsa_circ_83554,RMVar_hsa_circ_167929,RMVar_hsa_circ_375725,RMVar_hsa_circ_41906,RMVar_hsa_circ_167934,RMVar_hsa_circ_369844,RMVar_hsa_circ_268868,RMVar_hsa_circ_373094,RMVar_hsa_circ_167935,RMVar_hsa_circ_357410,RMVar_hsa_circ_167938 16808 RMVar_ID_16808 Human_SNP_ID_560845653 A-to-I Human chr14 + 74731025 74731025 74731025 ATCTCCAAAAAAAAAAAAAATTTAGTAGAGATAGGGTCTCACTATGTTGCCCAGCTGGTCTCAAA ATCTCCAAAAAAAAAAAAAATTTAGTAGAGATGGGGTCTCACTATGTTGCCCAGCTGGTCTCAAA A G FCF1 Ensembl:ENSG00000119616 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1038658857 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_30137 16809 RMVar_ID_16809 Human_SNP_ID_560846747 A-to-I Human chr14 + 74735609 74735609 74735609 TTTTTTTTCTTGAGATGAAGTTTTGCTCTGTCACCAGGCTGGAGTGCAGTGGCGTGATCTGGGCT TTTTTTTTCTTGAGATGAAGTTTTGCTCTGTCTCCAGGCTGGAGTGCAGTGGCGTGATCTGGGCT A T FCF1 Ensembl:ENSG00000119616 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1278540861 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_451789,Human_RBP_ID_4314336,Human_RBP_ID_22369986,Human_RBP_ID_26431705 16810 RMVar_ID_16810 Human_SNP_ID_560846763 A-to-I Human chr14 + 74735669 74735669 74735669 GGGCTCACTGCAACCCCTGCCTCCCATCCTTCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGC GGGCTCACTGCAACCCCTGCCTCCCATCCTTCGAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGC A G FCF1 Ensembl:ENSG00000119616 Protein coding 3'UTR GSE38233;GSE100210;GSE100210;GSE99789;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,29129909,29796672,31158229,31158229 RNA-Seq:(High) rs946766724 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17853394 16811 RMVar_ID_16811 Human_SNP_ID_560846769 A-to-I Human chr14 + 74735687 74735687 74735687 GCCTCCCATCCTTCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGTACACA GCCTCCCATCCTTCAAGTGATTCTCCTGCCTCGGCCTCCCGAGTAGCTGGGATTACAGGTACACA A G FCF1 Ensembl:ENSG00000119616 Protein coding 3'UTR GSE38233;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,32596459 RNA-Seq:(High) rs935335478 Functional Loss SNV dbSNP153 33..33 33 - - - 16812 RMVar_ID_16812 Human_SNP_ID_560846773 A-to-I Human chr14 + 74735699 74735699 74735699 TCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGTACACACCACCATGCTCA TCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTGGCTGGGATTACAGGTACACACCACCATGCTCA A G FCF1 Ensembl:ENSG00000119616 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,29129909,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs1196156543 Functional Loss SNV dbSNP153 33..33 33 - - - 16813 RMVar_ID_16813 Human_SNP_ID_560846776 A-to-I Human chr14 + 74735709 74735709 74735709 CTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGTACACACCACCATGCTCAACTAATTTTT CTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTGCAGGTACACACCACCATGCTCAACTAATTTTT A G FCF1 Ensembl:ENSG00000119616 Protein coding 3'UTR GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,29796672,31158229,31158229,32596459,32596459 RNA-Seq:(High) rs1262537068 Functional Loss SNV dbSNP153 33..33 33 - - - 16814 RMVar_ID_16814 Human_SNP_ID_560846817 A-to-I Human chr14 + 74735841 74735841 74735841 AGTATGCCTCGGCCTCCCAAAGTGCTGGAATTACAGACATGAGCCACTGTGCCTGGCCTGCTCAC AGTATGCCTCGGCCTCCCAAAGTGCTGGAATTGCAGACATGAGCCACTGTGCCTGGCCTGCTCAC A G FCF1 Ensembl:ENSG00000119616 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,29129909,31158229,31158229,32596459,32596459 RNA-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 16815 RMVar_ID_16815 Human_SNP_ID_560846818 A-to-I Human chr14 + 74735841 74735841 74735841 AGTATGCCTCGGCCTCCCAAAGTGCTGGAATTACAGACATGAGCCACTGTGCCTGGCCTGCTCAC AGTATGCCTCGGCCTCCCAAAGTGCTGGAATTTCAGACATGAGCCACTGTGCCTGGCCTGCTCAC A T FCF1 Ensembl:ENSG00000119616 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,29129909,31158229,31158229,32596459,32596459 RNA-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 16816 RMVar_ID_16816 Human_SNP_ID_560846863 A-to-I Human chr14 + 74736019 74736019 74736019 CGCCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTGCGGAGTAGCTGGGACTATAGGTGCGTG CGCCTCCCAGGTTCAAGCGATTCTCCTGCCTCGGCCTGCGGAGTAGCTGGGACTATAGGTGCGTG A G FCF1 Ensembl:ENSG00000119616 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs994356049 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_451794 16817 RMVar_ID_16817 Human_SNP_ID_560846868 A-to-I Human chr14 + 74736031 74736031 74736031 TCAAGCGATTCTCCTGCCTCAGCCTGCGGAGTAGCTGGGACTATAGGTGCGTGCCACCACGTCCA TCAAGCGATTCTCCTGCCTCAGCCTGCGGAGTCGCTGGGACTATAGGTGCGTGCCACCACGTCCA A C FCF1 Ensembl:ENSG00000119616 Protein coding 3'UTR GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs973688358 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_451794,Human_RBP_ID_4301884,Human_RBP_ID_26431709 16818 RMVar_ID_16818 Human_SNP_ID_560846869 A-to-I Human chr14 + 74736031 74736031 74736031 TCAAGCGATTCTCCTGCCTCAGCCTGCGGAGTAGCTGGGACTATAGGTGCGTGCCACCACGTCCA TCAAGCGATTCTCCTGCCTCAGCCTGCGGAGTGGCTGGGACTATAGGTGCGTGCCACCACGTCCA A G FCF1 Ensembl:ENSG00000119616 Protein coding 3'UTR GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs973688358 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_451794,Human_RBP_ID_4301884,Human_RBP_ID_26431709 16819 RMVar_ID_16819 Human_SNP_ID_560846919 A-to-I Human chr14 + 74736247 74736247 74736247 CCTGGACAACATGGCAAAACCCCACCTCTACTAAAAATACAAAAAAAATTAGCTGGGTATGGTGT CCTGGACAACATGGCAAAACCCCACCTCTACTCAAAATACAAAAAAAATTAGCTGGGTATGGTGT A C FCF1 Ensembl:ENSG00000119616 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041709323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26431713 16820 RMVar_ID_16820 Human_SNP_ID_560846922 A-to-I Human chr14 + 74736260 74736260 74736260 GCAAAACCCCACCTCTACTAAAAATACAAAAAAAATTAGCTGGGTATGGTGTCACGTGCCTGTAA GCAAAACCCCACCTCTACTAAAAATACAAAAAGAATTAGCTGGGTATGGTGTCACGTGCCTGTAA A G FCF1 Ensembl:ENSG00000119616 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1226713841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12420122,Human_RBP_ID_26431713 16821 RMVar_ID_16821 Human_SNP_ID_560846925 A-to-I Human chr14 + 74736265 74736265 74736265 ACCCCACCTCTACTAAAAATACAAAAAAAATTAGCTGGGTATGGTGTCACGTGCCTGTAATCCCA ACCCCACCTCTACTAAAAATACAAAAAAAATTCGCTGGGTATGGTGTCACGTGCCTGTAATCCCA A C FCF1 Ensembl:ENSG00000119616 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs997988995 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12420122,Human_RBP_ID_26431713 16822 RMVar_ID_16822 Human_SNP_ID_560846932 A-to-I Human chr14 + 74736291 74736291 74736291 AAAATTAGCTGGGTATGGTGTCACGTGCCTGTAATCCCAGCCACTGGGGAGGCTGAGGCAGGAGA AAAATTAGCTGGGTATGGTGTCACGTGCCTGTGATCCCAGCCACTGGGGAGGCTGAGGCAGGAGA A G FCF1 Ensembl:ENSG00000119616 Protein coding 3'UTR GSE38233;GSE100210;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,29129909,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs1467519301 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4301893,Human_RBP_ID_26431713 16823 RMVar_ID_16823 Human_SNP_ID_560846936 A-to-I Human chr14 + 74736301 74736301 74736301 GGGTATGGTGTCACGTGCCTGTAATCCCAGCCACTGGGGAGGCTGAGGCAGGAGAACCTCTTGAA GGGTATGGTGTCACGTGCCTGTAATCCCAGCCGCTGGGGAGGCTGAGGCAGGAGAACCTCTTGAA A G FCF1 Ensembl:ENSG00000119616 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1370812834 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26431713 Human_miRNA_ID_504494,Human_miRNA_ID_511707 16824 RMVar_ID_16824 Human_SNP_ID_560846943 A-to-I Human chr14 + 74736340 74736340 74736340 AGGCTGAGGCAGGAGAACCTCTTGAACCCAGGAGGTGGAGGTTGCAGTGAGCTGAGATTGCGCCA AGGCTGAGGCAGGAGAACCTCTTGAACCCAGGGGGTGGAGGTTGCAGTGAGCTGAGATTGCGCCA A G FCF1 Ensembl:ENSG00000119616 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1258906287 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_121321 16825 RMVar_ID_16825 Human_SNP_ID_560846947 A-to-I Human chr14 + 74736362 74736362 74736362 TGAACCCAGGAGGTGGAGGTTGCAGTGAGCTGAGATTGCGCCACTGCATTCCAGCCTGGGTGACA TGAACCCAGGAGGTGGAGGTTGCAGTGAGCTGGGATTGCGCCACTGCATTCCAGCCTGGGTGACA A G FCF1 Ensembl:ENSG00000119616 Protein coding 3'UTR GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1038202055 Functional Loss SNV dbSNP153 33..33 33 - - - 16826 RMVar_ID_16826 Human_SNP_ID_560846951 A-to-I Human chr14 + 74736372 74736372 74736372 AGGTGGAGGTTGCAGTGAGCTGAGATTGCGCCACTGCATTCCAGCCTGGGTGACAGAGTGAGACT AGGTGGAGGTTGCAGTGAGCTGAGATTGCGCCCCTGCATTCCAGCCTGGGTGACAGAGTGAGACT A C FCF1 Ensembl:ENSG00000119616 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs929699736 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4314340 16827 RMVar_ID_16827 Human_SNP_ID_560847157 A-to-I Human chr14 + 74737287 74737287 74737287 TGAGGCAGGAGAATCGCTTGAACCCGGGAGGCAGAGGTTGCAACGAGCCGAGATCACGCCACTGC TGAGGCAGGAGAATCGCTTGAACCCGGGAGGCGGAGGTTGCAACGAGCCGAGATCACGCCACTGC A G FCF1 Ensembl:ENSG00000119616 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs374571599 Functional Loss SNV dbSNP153 33..33 33 - - - 16828 RMVar_ID_16828 Human_SNP_ID_560859809 A-to-I Human chr14 + 74787407 74787407 74787407 CAACATGGTGAAGCCCCAGCTCTACCAAAAATACAAAAATTAGCTAGGCATGGTGGTGCACGCTT CAACATGGTGAAGCCCCAGCTCTACCAAAAATGCAAAAATTAGCTAGGCATGGTGGTGCACGCTT A G YLPM1 Ensembl:ENSG00000119596 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1242239970 Functional Loss SNV dbSNP153 33..33 33 - - - 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_167942 16829 RMVar_ID_16829 Human_SNP_ID_560864703 A-to-I Human chr14 + 74806481 74806481 74806481 GCGCCAGGTGGTGCGCACCTGTAATCCCAGCTACTAGGGAGACTGAGGCAGGAGAATTGCTTGAA GCGCCAGGTGGTGCGCACCTGTAATCCCAGCTGCTAGGGAGACTGAGGCAGGAGAATTGCTTGAA A G YLPM1 Ensembl:ENSG00000119596 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs993358848 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8535,RMVar_hsa_circ_45050,RMVar_hsa_circ_93731,RMVar_hsa_circ_167944,RMVar_hsa_circ_357377,RMVar_hsa_circ_364701,RMVar_hsa_circ_72065,RMVar_hsa_circ_350698,RMVar_hsa_circ_59541 16830 RMVar_ID_16830 Human_SNP_ID_560865974 A-to-I Human chr14 + 74811280 74811280 74811280 AAGGCAGGTGGATCTCTTGAGCTCAGGAGTTCAAGACCAGCCTGGCCAACATGGCGAAACCCCAT AAGGCAGGTGGATCTCTTGAGCTCAGGAGTTCCAGACCAGCCTGGCCAACATGGCGAAACCCCAT A C YLPM1 Ensembl:ENSG00000119596 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1006301311 Functional Loss SNV dbSNP153 33..33 33 - - - 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_59541,RMVar_hsa_circ_40636,RMVar_hsa_circ_167947,RMVar_hsa_circ_318406,RMVar_hsa_circ_17700,RMVar_hsa_circ_167946,RMVar_hsa_circ_51677 16831 RMVar_ID_16831 Human_SNP_ID_560868664 A-to-I Human chr14 + 74822624 74822624 74822624 AATGAATACACTTGTCTGCCTGACTTGATTATAAAACTTCTCTTAACCCATTCAAAGATGCAGAA AATGAATACACTTGTCTGCCTGACTTGATTATGAAACTTCTCTTAACCCATTCAAAGATGCAGAA A G YLPM1 Ensembl:ENSG00000119596 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1478257992 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8077723,Human_RBP_ID_12421059,Human_RBP_ID_17853454 RMVar_hsa_circ_357377,RMVar_hsa_circ_72065,RMVar_hsa_circ_17700,RMVar_hsa_circ_44316,RMVar_hsa_circ_44818,RMVar_hsa_circ_45930,RMVar_hsa_circ_17049 16832 RMVar_ID_16832 Human_SNP_ID_560880691 A-to-I Human chr14 - 74874092 74874092 74874092 TTTCCAAAGCGGTCTTTAGAAAAGCCATATCTATCCCTTTATTATTTTTGGTCCCAAAAGGCGGA TTTCCAAAGCGGTCTTTAGAAAAGCCATATCTGTCCCTTTATTATTTTTGGTCCCAAAAGGCGGA T C PROX2 Ensembl:ENSG00000119608 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1238928527 Functional Loss SNV dbSNP153 33..33 33 - - - 16833 RMVar_ID_16833 Human_SNP_ID_560886178 A-to-I Human chr14 + 74894754 74894754 74894754 TTTTTTTAGTGGAGACGGGGTTTCACCGTGTTAGCCAGGATGGTCTCGATCTCCTGACCTCGTGA TTTTTTTAGTGGAGACGGGGTTTCACCGTGTTTGCCAGGATGGTCTCGATCTCCTGACCTCGTGA A T DLST Ensembl:ENSG00000119689 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1419303256 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5420,RMVar_hsa_circ_4861,RMVar_hsa_circ_69921,RMVar_hsa_circ_50790 16834 RMVar_ID_16834 Human_SNP_ID_560886281 A-to-I Human chr14 + 74895071 74895071 74895071 TAACAAGGCGAAACCCCACCTCTACAAAAAATACAAAAATTAGCCAGGTGTGGTGGTGCACATCT TAACAAGGCGAAACCCCACCTCTACAAAAAATGCAAAAATTAGCCAGGTGTGGTGGTGCACATCT A G DLST Ensembl:ENSG00000119689 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1212222314 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25114590 RMVar_hsa_circ_5420,RMVar_hsa_circ_4861,RMVar_hsa_circ_69921,RMVar_hsa_circ_50790 16835 RMVar_ID_16835 Human_SNP_ID_560886294 A-to-I Human chr14 + 74895116 74895116 74895116 AGGTGTGGTGGTGCACATCTGTAGCCCCAGCTACTTGGGGGGCTGAGATGGGAGGATTGTTTGAC AGGTGTGGTGGTGCACATCTGTAGCCCCAGCTGCTTGGGGGGCTGAGATGGGAGGATTGTTTGAC A G DLST Ensembl:ENSG00000119689 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1402309160 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5420,RMVar_hsa_circ_4861,RMVar_hsa_circ_69921,RMVar_hsa_circ_50790 16836 RMVar_ID_16836 Human_SNP_ID_560886407 A-to-I Human chr14 + 74895577 74895577 74895577 TAGGAGTTGGAAACCAGCCTGGGCAACATAGCAAGACTGTCTCTACATAAAATTTAAAAATTAGC TAGGAGTTGGAAACCAGCCTGGGCAACATAGCGAGACTGTCTCTACATAAAATTTAAAAATTAGC A G DLST Ensembl:ENSG00000119689 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1316790766 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5420,RMVar_hsa_circ_4861,RMVar_hsa_circ_69921,RMVar_hsa_circ_50790 16837 RMVar_ID_16837 Human_SNP_ID_560886522 A-to-I Human chr14 + 74896046 74896046 74896046 GCTTGGCCAATTTTTTTAGTTTTTGTAGAGACAAGGTCTCGCTGTGTTGCCTAGGCTGGTCTCCT GCTTGGCCAATTTTTTTAGTTTTTGTAGAGACGAGGTCTCGCTGTGTTGCCTAGGCTGGTCTCCT A G DLST Ensembl:ENSG00000119689 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1325197019 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5420,RMVar_hsa_circ_4861,RMVar_hsa_circ_69921,RMVar_hsa_circ_50790 16838 RMVar_ID_16838 Human_SNP_ID_294603075 A-to-I Human chr6 + 122475120 122475120 122475120 CAGTGGCCTGATCTCGGCTCACTGCAACCTCCACCTCCCAAATTCCAGCGATTCTCCTGCAACCG CAGTGGCCTGATCTCGGCTCACTGCAACCTCCGCCTCCCAAATTCCAGCGATTCTCCTGCAACCG A G PKIB,Z99129.3 Ensembl:ENSG00000135549,Ensembl:ENSG00000279114 Protein coding,Other intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs936859418 Functional Loss SNV dbSNP153 33..33 33 - - - 16839 RMVar_ID_16839 Human_SNP_ID_294694553 A-to-I Human chr6 + 122859913 122859913 122859913 AAACTTGGCGTAGTACCAAAATGTGGCCAATCAAGGCTTTGAGTAAGTCACAGCAGCGTTCACCA AAACTTGGCGTAGTACCAAAATGTGGCCAATCGAGGCTTTGAGTAAGTCACAGCAGCGTTCACCA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879143572 Functional Loss SNV dbSNP153 33..33 33 - - - 16840 RMVar_ID_16840 Human_SNP_ID_294694566 A-to-I Human chr6 + 122859948 122859948 122859948 GCTTTGAGTAAGTCACAGCAGCGTTCACCAGCACCAGGGTCTTTTCCACAAGGTTACGGAAAAAT GCTTTGAGTAAGTCACAGCAGCGTTCACCAGCGCCAGGGTCTTTTCCACAAGGTTACGGAAAAAT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878938147 Functional Loss SNV dbSNP153 33..33 33 - - - 16841 RMVar_ID_16841 Human_SNP_ID_294694569 A-to-I Human chr6 + 122859951 122859951 122859951 TTGAGTAAGTCACAGCAGCGTTCACCAGCACCAGGGTCTTTTCCACAAGGTTACGGAAAAATTGG TTGAGTAAGTCACAGCAGCGTTCACCAGCACCGGGGTCTTTTCCACAAGGTTACGGAAAAATTGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879028364 Functional Loss SNV dbSNP153 33..33 33 - - - 16842 RMVar_ID_16842 Human_SNP_ID_294940876 A-to-I Human chr6 + 123852608 123852608 123852608 TATTCACAATAGCCATAATGTGGAATTAACCTAAGTGCCCATCAATGGATGATGACTGGATAAAG TATTCACAATAGCCATAATGTGGAATTAACCTTAGTGCCCATCAATGGATGATGACTGGATAAAG A T NKAIN2 Ensembl:ENSG00000188580 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank;ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1262834333 Functional Loss SNV dbSNP153 33..33 33 - - - 16843 RMVar_ID_16843 Human_SNP_ID_294955062 A-to-I Human chr6 + 123911308 123911308 123911308 TCTGCAGGCTGTACAAGAAACATGGTGTCAGCATCTACTTCTGGTGAGGGCCTCAGGAAGCTTCC TCTGCAGGCTGTACAAGAAACATGGTGTCAGCGTCTACTTCTGGTGAGGGCCTCAGGAAGCTTCC A G NKAIN2 Ensembl:ENSG00000188580 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1473651395 Functional Loss SNV dbSNP153 33..33 33 - - - 16844 RMVar_ID_16844 Human_SNP_ID_294977748 A-to-I Human chr6 + 124005043 124005043 124005043 GTTCAGGAGTTTGAGACCAGCTTGGTCAAGATAGTGAAACCCTGTCTTTACTAAAAATACAAAAA GTTCAGGAGTTTGAGACCAGCTTGGTCAAGATGGTGAAACCCTGTCTTTACTAAAAATACAAAAA A G NKAIN2 Ensembl:ENSG00000188580 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1280098699 Functional Loss SNV dbSNP153 33..33 33 - - - 16845 RMVar_ID_16845 Human_SNP_ID_295002593 A-to-I Human chr6 + 124109916 124109916 124109916 TGATTTGCTGTATCACGTTAACTGATTTGGGCATGTTGAACATCCTTGCATCACAGGAATAAATG TGATTTGCTGTATCACGTTAACTGATTTGGGCGTGTTGAACATCCTTGCATCACAGGAATAAATG A G NKAIN2 Ensembl:ENSG00000188580 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs556556690 Functional Loss SNV dbSNP153 33..33 33 - - - 16846 RMVar_ID_16846 Human_SNP_ID_295002681 A-to-I Human chr6 + 124110214 124110214 124110214 TATTATCGAGTGCAGTTTATCCCAGGGATGTAAAGATAATTTGACACAGGCACATCAATAAATGT TATTATCGAGTGCAGTTTATCCCAGGGATGTAGAGATAATTTGACACAGGCACATCAATAAATGT A G NKAIN2 Ensembl:ENSG00000188580 Protein coding intron GSE107867 ASD brains,cerebellum;ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1214560431 Functional Loss SNV dbSNP153 33..33 33 - - - 16847 RMVar_ID_16847 Human_SNP_ID_295081940 A-to-I Human chr6 + 124425118 124425118 124425118 AAAAGATCGTTGCAACAATCTTTGGAAAATCCAATCTGCCACATATTTCAAGGGAGAAGACAGTT AAAAGATCGTTGCAACAATCTTTGGAAAATCCGATCTGCCACATATTTCAAGGGAGAAGACAGTT A G NKAIN2 Ensembl:ENSG00000188580 Protein coding intron GSE107867 ASD brains,cerebellum;ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1446859670 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11071,RMVar_hsa_circ_296127,RMVar_hsa_circ_42204,RMVar_hsa_circ_52960 16848 RMVar_ID_16848 Human_SNP_ID_295098070 A-to-I Human chr6 + 124492361 124492361 124492361 ATGAGTTTTTTCTAGAAAACATCTTCCTGCCTAGAGTTCAGTCAAATTTCCTACAGTTCAGTTAA ATGAGTTTTTTCTAGAAAACATCTTCCTGCCTTGAGTTCAGTCAAATTTCCTACAGTTCAGTTAA A T NKAIN2 Ensembl:ENSG00000188580 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs888074279 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11071,RMVar_hsa_circ_296127,RMVar_hsa_circ_42204,RMVar_hsa_circ_52960 16849 RMVar_ID_16849 Human_SNP_ID_295159186 A-to-I Human chr6 - 124743906 124743906 124743906 TCACAATTTTATAAATTAATAAACTGTCATTTATTCTACAGCAAACTCTTCTAGCTTTGGTCTAT TCACAATTTTATAAATTAATAAACTGTCATTTTTTCTACAGCAAACTCTTCTAGCTTTGGTCTAT T A RNF217-AS1 Ensembl:ENSG00000236548 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs901818067 Functional Loss SNV dbSNP153 33..33 33 - - - 16850 RMVar_ID_16850 Human_SNP_ID_295429666 A-to-I Human chr6 + 125896558 125896558 125896558 CATGCCTGTAATCCCAGCACTTTTGGGAGGCCAAGGTGGACAGATTGCTTGAGCTCAGCAGTTCA CATGCCTGTAATCCCAGCACTTTTGGGAGGCCGAGGTGGACAGATTGCTTGAGCTCAGCAGTTCA A G NCOA7 Ensembl:ENSG00000111912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs961031485 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15629863 RMVar_hsa_circ_37853,RMVar_hsa_circ_269491,RMVar_hsa_circ_64132 16851 RMVar_ID_16851 Human_SNP_ID_295429671 A-to-I Human chr6 + 125896590 125896589 125896590 AAGGTGGACAGATTGCTTGAGCTCAGCAGTTCAAGACAAGCCTGGGCAACATGGTGAAATCACAT AAGGTGGACAGATTGCTTGAGCTCAGCAGTTC_AGACAAGCCTGGGCAACATGGTGAAATCACAT CA C NCOA7 Ensembl:ENSG00000111912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1467655333 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_37853,RMVar_hsa_circ_269491,RMVar_hsa_circ_64132 16852 RMVar_ID_16852 Human_SNP_ID_295451513 A-to-I Human chr6 + 125991307 125991307 125991307 CTGTTCTCTCTCTGTTTTCCAGGCTACAGTGCAGTGGCGTGACCGTGGCTCACTGCAGCCTCAAA CTGTTCTCTCTCTGTTTTCCAGGCTACAGTGCGGTGGCGTGACCGTGGCTCACTGCAGCCTCAAA A G TRMT11 Ensembl:ENSG00000066651 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs987793382 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26764450 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 16853 RMVar_ID_16853 Human_SNP_ID_295470600 A-to-I Human chr6 + 126075419 126075419 126075419 ATTGGATCATGGGGACGGATTTCCCCCTTGCTATTCTCGTGATAGTGAGTTCTCATGAGATCCGA ATTGGATCATGGGGACGGATTTCCCCCTTGCTCTTCTCGTGATAGTGAGTTCTCATGAGATCCGA A C TRMT11 Ensembl:ENSG00000066651 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1480494236 Functional Loss SNV dbSNP153 33..33 33 - - - 16854 RMVar_ID_16854 Human_SNP_ID_295497124 A-to-I Human chr6 + 126194985 126194985 126194985 AAAAATAAAAAAAATTAGCTGGGTGTGGTGGCATGCCCCTGTTGTCCCAGCTACTCAGGAGGCTG AAAAATAAAAAAAATTAGCTGGGTGTGGTGGCCTGCCCCTGTTGTCCCAGCTACTCAGGAGGCTG A C TRMT11 Ensembl:ENSG00000066651 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs867804863 Functional Loss SNV dbSNP153 33..33 33 - - - 16855 RMVar_ID_16855 Human_SNP_ID_295747751 A-to-I Human chr6 + 127271249 127271247 127271250 TCAGTAAAGCTTCCAGGCAATAGTAGACTATTAGTAGTTAAGTTTTTGGAAACTCAAAAGTTTAC TCAGTAAAGCTTCCAGGCAATAGTAGACTAT___TAGTTAAGTTTTTGGAAACTCAAAAGTTTAC TTAG T RNF146 Ensembl:ENSG00000118518 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1454208990 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_15640225 16856 RMVar_ID_16856 Human_SNP_ID_295753453 A-to-I Human chr6 - 127296322 127296322 127296322 CCGGGTGTGATGGCGCACGTGTAGTTGCAGCTACTCTGGAGGCTGAGGCAGGAGAGTCACTTGAA CCGGGTGTGATGGCGCACGTGTAGTTGCAGCTGCTCTGGAGGCTGAGGCAGGAGAGTCACTTGAA T C ECHDC1 Ensembl:ENSG00000093144 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1303738566 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15640496 16857 RMVar_ID_16857 Human_SNP_ID_295755725 A-to-I Human chr6 - 127306662 127306662 127306662 AGAAGAGAGGTTTAATTGGCTCATAGTCCCACAGGCTGTACAGGAAGCATGGCTGGGGAATCCTC AGAAGAGAGGTTTAATTGGCTCATAGTCCCACCGGCTGTACAGGAAGCATGGCTGGGGAATCCTC T G ECHDC1 Ensembl:ENSG00000093144 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs566217257 Functional Loss SNV dbSNP153 33..33 33 - - - 16858 RMVar_ID_16858 Human_SNP_ID_295756570 A-to-I Human chr6 - 127309912 127309912 127309912 TCATGGGGGCAGACTTCCCCCTTGCTCTTCTCATGATAAGTGCGTAAGTTCTCACAAGAACTGGT TCATGGGGGCAGACTTCCCCCTTGCTCTTCTCGTGATAAGTGCGTAAGTTCTCACAAGAACTGGT T C ECHDC1 Ensembl:ENSG00000093144 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909703791 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17576449 16859 RMVar_ID_16859 Human_SNP_ID_295787407 A-to-I Human chr6 - 127438568 127438568 127438568 ATTTATATAATTACACTCTGTGATGTTCGCTCAGTGATGAAATCACCTGAGAACACGTTTCTCAG ATTTATATAATTACACTCTGTGATGTTCGCTCGGTGATGAAATCACCTGAGAACACGTTTCTCAG T C KIAA0408,AL096711.2 Ensembl:ENSG00000189367,Ensembl:ENSG00000255330 Protein coding,Protein coding 3'UTR,3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs527665983 Functional Loss SNV dbSNP153 33..33 33 - - - 16860 RMVar_ID_16860 Human_SNP_ID_295986550 A-to-I Human chr6 - 128255129 128255129 128255129 AAAATTGGCTGGGCATGGTGGCGGGCGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGA AAAATTGGCTGGGCATGGTGGCGGGCGCCTGTGGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGA T C PTPRK Ensembl:ENSG00000152894 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1233715633 Functional Loss SNV dbSNP153 33..33 33 - - - 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 16861 RMVar_ID_16861 Human_SNP_ID_296032746 A-to-I Human chr6 - 128449063 128449063 128449063 GAGGTCAGGAGTTTGAGACCAGCCTGACCAACATGGTGAAACCCCGTCTCTACTGGGGGAAAAAA GAGGTCAGGAGTTTGAGACCAGCCTGACCAACGTGGTGAAACCCCGTCTCTACTGGGGGAAAAAA T C PTPRK Ensembl:ENSG00000152894 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1280669484 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98736,RMVar_hsa_circ_241396 16862 RMVar_ID_16862 Human_SNP_ID_296152258 A-to-I Human chr6 + 128929385 128929385 128929385 ACCTCGAGAGAATACAAAGAAGTTCATCAGTCATGTGAGGATGAGTGATAGCACACCTCCATCTT ACCTCGAGAGAATACAAAGAAGTTCATCAGTCGTGTGAGGATGAGTGATAGCACACCTCCATCTT A G LAMA2 Ensembl:ENSG00000196569 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1160848173 Functional Loss SNV dbSNP153 33..33 33 - - - 16863 RMVar_ID_16863 Human_SNP_ID_296296420 A-to-I Human chr6 - 129520371 129520371 129520371 TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTAGAGCTAAGGTCTCACTGTGTGGCTCAGGCTGGTC TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTAGCGCTAAGGTCTCACTGTGTGGCTCAGGCTGGTC T G AL356124.1 Ensembl:ENSG00000226149 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1158014685 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119791,RMVar_hsa_circ_241438,RMVar_hsa_circ_80002,RMVar_hsa_circ_241439,RMVar_hsa_circ_241440,RMVar_hsa_circ_241441 16864 RMVar_ID_16864 Human_SNP_ID_296326586 A-to-I Human chr6 - 129637264 129637263 129637265 ACTGGAGAGTTCGAGACCAGCCTGGGCAACATAGCAAAACCCAATCTCTACAAAAAGCGCAAGAA ACTGGAGAGTTCGAGACCAGCCTGGGCAACA__GCAAAACCCAATCTCTACAAAAAGCGCAAGAA CTA C ARHGAP18 Ensembl:ENSG00000146376 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1412953401 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_73509,RMVar_hsa_circ_354411,RMVar_hsa_circ_241450,RMVar_hsa_circ_21597,RMVar_hsa_circ_317509,RMVar_hsa_circ_241455,RMVar_hsa_circ_241454,RMVar_hsa_circ_273772 16865 RMVar_ID_16865 Human_SNP_ID_296338228 A-to-I Human chr6 - 129685431 129685431 129685431 GTGATCTCAGCTCACTGCAACCCCTGGCTCCCAGGTTTAAGTGATTCTCCTAGCTCAGCCTCCCA GTGATCTCAGCTCACTGCAACCCCTGGCTCCCGGGTTTAAGTGATTCTCCTAGCTCAGCCTCCCA T C ARHGAP18 Ensembl:ENSG00000146376 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs972263620 Functional Loss SNV dbSNP153 33..33 33 - - - 16866 RMVar_ID_16866 Human_SNP_ID_296627384 A-to-I Human chr6 - 130875833 130875833 130875833 CTACCAAGTCTGGCTAATTTTTTTGTGTTTTTAGTTGAGACGGGGTTTCACTATGTTGACCAGAC CTACCAAGTCTGGCTAATTTTTTTGTGTTTTTGGTTGAGACGGGGTTTCACTATGTTGACCAGAC T C EPB41L2 Ensembl:ENSG00000079819 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1205423837 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15644014 RMVar_hsa_circ_12549,RMVar_hsa_circ_64254,RMVar_hsa_circ_13144,RMVar_hsa_circ_364473 16867 RMVar_ID_16867 Human_SNP_ID_296627411 A-to-I Human chr6 - 130875946 130875940 130875946 CACTCTTGCACATTCGCCCGGGCTGGAGTGCAATGGCATGATCTTGGCTCACTGCAACCTCCATC CACTCTTGCACATTCGCCCGGGCTGGAGTGCA______TGATCTTGGCTCACTGCAACCTCCATC ATGCCAT A EPB41L2 Ensembl:ENSG00000079819 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,frontal_cortex - 29129909,30559470 RNA-Seq:(High) rs550291748 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_7540151,Human_RBP_ID_15644015,Human_RBP_ID_25963354 RMVar_hsa_circ_12549,RMVar_hsa_circ_64254,RMVar_hsa_circ_13144,RMVar_hsa_circ_364473 16868 RMVar_ID_16868 Human_SNP_ID_296627412 A-to-I Human chr6 - 130875946 130875946 130875946 CACTCTTGCACATTCGCCCGGGCTGGAGTGCAATGGCATGATCTTGGCTCACTGCAACCTCCATC CACTCTTGCACATTCGCCCGGGCTGGAGTGCAGTGGCATGATCTTGGCTCACTGCAACCTCCATC T C EPB41L2 Ensembl:ENSG00000079819 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,frontal_cortex - 29129909,30559470 RNA-Seq:(High) rs900287059 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7540151,Human_RBP_ID_15644015,Human_RBP_ID_25963354 RMVar_hsa_circ_12549,RMVar_hsa_circ_64254,RMVar_hsa_circ_13144,RMVar_hsa_circ_364473 16869 RMVar_ID_16869 Human_SNP_ID_296895433 A-to-I Human chr6 - 131950162 131950162 131950162 TTTTACATGGTGTTTGTGTGCTCTGCTCTCGCAGCTTACCGACTGGAAGACACGTTTGGCCCAGA TTTTACATGGTGTTTGTGTGCTCTGCTCTCGCGGCTTACCGACTGGAAGACACGTTTGGCCCAGA T C CCN2 Ensembl:ENSG00000118523 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1385747051 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_951353,Human_RBP_ID_22554376 RMVar_hsa_circ_110303,RMVar_hsa_circ_241547 16870 RMVar_ID_16870 Human_SNP_ID_297021553 A-to-I Human chr6 - 132473076 132473076 132473076 CAGCTCATTGCATCCTCCACCTCCCATGTTCAAGTGATTCTTCTGCCTCAGCCACCCAAGTAGCT CAGCTCATTGCATCCTCCACCTCCCATGTTCACGTGATTCTTCTGCCTCAGCCACCCAAGTAGCT T G STX7 Ensembl:ENSG00000079950 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1161412759 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_241565,RMVar_hsa_circ_309205,RMVar_hsa_circ_241568,RMVar_hsa_circ_344894,RMVar_hsa_circ_59365 16871 RMVar_ID_16871 Human_SNP_ID_297107140 A-to-I Human chr6 - 132794271 132794271 132794271 GGTGAAACCCTGTCTGTACTAAAAATACAAAAATTAGCCAGGCATGGTGGCACGTGACTGTAGTC GGTGAAACCCTGTCTGTACTAAAAATACAAAAGTTAGCCAGGCATGGTGGCACGTGACTGTAGTC T C SLC18B1 Ensembl:ENSG00000146409 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1351654012 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1958,RMVar_hsa_circ_51437 16872 RMVar_ID_16872 Human_SNP_ID_297229181 A-to-I Human chr6 + 133284268 133284268 133284268 CTCGGCTCACTGCAACCTCTGCCTCCTGAGTTAAGTGATTCTCCTGTCTCAGCCCCCCGAGTAGA CTCGGCTCACTGCAACCTCTGCCTCCTGAGTTGAGTGATTCTCCTGTCTCAGCCCCCCGAGTAGA A G EYA4 Ensembl:ENSG00000112319 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1235771220 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1637,RMVar_hsa_circ_241586,RMVar_hsa_circ_374745 16873 RMVar_ID_16873 Human_SNP_ID_297231470 A-to-I Human chr6 + 133293819 133293819 133293819 ATTAGACAGGCATGGTGGCATGCACCTGTAGTACCAGCTACTTGGGAGGCTGAGGTTGGAGGATC ATTAGACAGGCATGGTGGCATGCACCTGTAGTGCCAGCTACTTGGGAGGCTGAGGTTGGAGGATC A G EYA4 Ensembl:ENSG00000112319 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1245718067 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1637,RMVar_hsa_circ_241586,RMVar_hsa_circ_374745 16874 RMVar_ID_16874 Human_SNP_ID_297231835 A-to-I Human chr6 + 133294707 133294707 133294707 CTCCTGCCTCAGCCTCCAGAGTACCTGGGACTACAGGCATGAACCACCATGCGTGGCTAATTTTT CTCCTGCCTCAGCCTCCAGAGTACCTGGGACTGCAGGCATGAACCACCATGCGTGGCTAATTTTT A G EYA4 Ensembl:ENSG00000112319 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs957415723 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1637,RMVar_hsa_circ_241586,RMVar_hsa_circ_374745 16875 RMVar_ID_16875 Human_SNP_ID_297389569 A-to-I Human chr6 + 133963461 133963461 133963461 CTTTTTATTTGTTTAAGACATAGTCTCACTCTATAGCCCAGACTGGAGTGCAGTGGTGTGATCAT CTTTTTATTTGTTTAAGACATAGTCTCACTCTGTAGCCCAGACTGGAGTGCAGTGGTGTGATCAT A G TBPL1,AL035699.1 Ensembl:ENSG00000028839,Ensembl:ENSG00000288529 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005346780 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_241593,RMVar_hsa_circ_103422 16876 RMVar_ID_16876 Human_SNP_ID_297389597 A-to-I Human chr6 + 133963611 133963611 133963611 TCTGGCTAATTTTTGTATTTTTTTGTCGAGACAGAGTCTCACCATGTTGCTCAGTCTGGTCTGTA TCTGGCTAATTTTTGTATTTTTTTGTCGAGACGGAGTCTCACCATGTTGCTCAGTCTGGTCTGTA A G TBPL1,AL035699.1 Ensembl:ENSG00000028839,Ensembl:ENSG00000288529 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1358663598 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_241593,RMVar_hsa_circ_103422 16877 RMVar_ID_16877 Human_SNP_ID_297443341 A-to-I Human chr6 - 134182137 134182137 134182137 TCTCACAGGTATGGCTAGGCACAGTGGCTCACACTTGTAATCCCAGCACTTTGGGAGGCTGAGGA TCTCACAGGTATGGCTAGGCACAGTGGCTCACGCTTGTAATCCCAGCACTTTGGGAGGCTGAGGA T C SGK1 Ensembl:ENSG00000118515 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971122949 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33385 16878 RMVar_ID_16878 Human_SNP_ID_297447101 A-to-I Human chr6 - 134197227 134197227 134197227 TGTTGCTGTTGCTGTTGTTGGTTGTTTGAGACAGGGTCTTATTTTGTCACCCAGGCTGGAGTGCG TGTTGCTGTTGCTGTTGTTGGTTGTTTGAGACTGGGTCTTATTTTGTCACCCAGGCTGGAGTGCG T A SGK1 Ensembl:ENSG00000118515 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs939322801 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33385 16879 RMVar_ID_16879 Human_SNP_ID_297451921 A-to-I Human chr6 - 134214374 134214374 134214374 GCTGGCTAGGCTGGTCTCGAACGCCTGACCTCAGTTGATCCGCCTGCCTCGGCCTCCCAAATTGC GCTGGCTAGGCTGGTCTCGAACGCCTGACCTCGGTTGATCCGCCTGCCTCGGCCTCCCAAATTGC T C SGK1 Ensembl:ENSG00000118515 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1386748782 Functional Loss SNV dbSNP153 33..33 33 - - - 16880 RMVar_ID_16880 Human_SNP_ID_297451966 A-to-I Human chr6 - 134214574 134214574 134214574 TTACTTTCATTAATTTTTTTTTTTTTTGAGACAGCGTATCCCTCTGTCACCCAGGCTAGAGTACG TTACTTTCATTAATTTTTTTTTTTTTTGAGACTGCGTATCCCTCTGTCACCCAGGCTAGAGTACG T A SGK1 Ensembl:ENSG00000118515 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1304040335 Functional Loss SNV dbSNP153 33..33 33 - - - 16881 RMVar_ID_16881 Human_SNP_ID_297451967 A-to-I Human chr6 - 134214574 134214574 134214574 TTACTTTCATTAATTTTTTTTTTTTTTGAGACAGCGTATCCCTCTGTCACCCAGGCTAGAGTACG TTACTTTCATTAATTTTTTTTTTTTTTGAGACGGCGTATCCCTCTGTCACCCAGGCTAGAGTACG T C SGK1 Ensembl:ENSG00000118515 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1304040335 Functional Loss SNV dbSNP153 33..33 33 - - - 16882 RMVar_ID_16882 Human_SNP_ID_297458799 A-to-I Human chr6 - 134241201 134241201 134241201 TACAGAAAATATAAAAAATAGCCGGATGTGGTAGTGGATGCCTGTAGTCCCAGCTACTCAGGAGG TACAGAAAATATAAAAAATAGCCGGATGTGGTCGTGGATGCCTGTAGTCCCAGCTACTCAGGAGG T G SGK1 Ensembl:ENSG00000118515 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs911522549 Functional Loss SNV dbSNP153 33..33 33 - - - 16883 RMVar_ID_16883 Human_SNP_ID_297461103 A-to-I Human chr6 - 134250922 134250922 134250922 AAATACGATGAAATAAATTAGCCGTGTATAGTAGTGCACACCTATAGTCCCAGCTACCTGAGAGG AAATACGATGAAATAAATTAGCCGTGTATAGTTGTGCACACCTATAGTCCCAGCTACCTGAGAGG T A SGK1 Ensembl:ENSG00000118515 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1449092907 Functional Loss SNV dbSNP153 33..33 33 - - - 16884 RMVar_ID_16884 Human_SNP_ID_297462230 A-to-I Human chr6 - 134255624 134255624 134255624 TGACCCAGGATCATGCCATTGTACTCCAGCCTAGGTGACAAGAGCGAGGCTCCATCTCAAAAAAA TGACCCAGGATCATGCCATTGTACTCCAGCCTGGGTGACAAGAGCGAGGCTCCATCTCAAAAAAA T C SGK1 Ensembl:ENSG00000118515 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978825758 Functional Loss SNV dbSNP153 33..33 33 - - - 16885 RMVar_ID_16885 Human_SNP_ID_297463125 A-to-I Human chr6 - 134259520 134259520 134259520 CCTGCCTCAGCCTCCTGAGTAGCCGGGATTACAGGCATCTGACACCACACCCGGGTAATTTTTTT CCTGCCTCAGCCTCCTGAGTAGCCGGGATTACTGGCATCTGACACCACACCCGGGTAATTTTTTT T A SGK1 Ensembl:ENSG00000118515 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285684368 Functional Loss SNV dbSNP153 33..33 33 - - - 16886 RMVar_ID_16886 Human_SNP_ID_297463126 A-to-I Human chr6 - 134259522 134259522 134259522 CTCCTGCCTCAGCCTCCTGAGTAGCCGGGATTACAGGCATCTGACACCACACCCGGGTAATTTTT CTCCTGCCTCAGCCTCCTGAGTAGCCGGGATTGCAGGCATCTGACACCACACCCGGGTAATTTTT T C SGK1 Ensembl:ENSG00000118515 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1043544628 Functional Loss SNV dbSNP153 33..33 33 - - - 16887 RMVar_ID_16887 Human_SNP_ID_297481380 A-to-I Human chr6 - 134335142 134335142 134335142 TGGTGGCACACATTTATGGTCCCAGCTACTCCAGAGGCTGAGGAGAGAGGGTAGCAGGAACCCAG TGGTGGCACACATTTATGGTCCCAGCTACTCCGGAGGCTGAGGAGAGAGGGTAGCAGGAACCCAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs772932441 Functional Loss SNV dbSNP153 33..33 33 - - - 16888 RMVar_ID_16888 Human_SNP_ID_297486120 A-to-I Human chr6 + 134355147 134355147 134355147 TTTTGCAGAGACGAGCTTTTGCCATGTTACCTAAGCTGGTCTTGAACTCCTGAGCTCAGGTATTC TTTTGCAGAGACGAGCTTTTGCCATGTTACCTGAGCTGGTCTTGAACTCCTGAGCTCAGGTATTC A G LINC01010 Ensembl:ENSG00000236700 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1000167918 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15651945 16889 RMVar_ID_16889 Human_SNP_ID_297489618 A-to-I Human chr6 + 134369787 134369787 134369787 GGAGTTCGAGACCAGCCTGGGCAACATGGTGAAACCCTTTCTCTACTAAAATACAAAAAAAAACA GGAGTTCGAGACCAGCCTGGGCAACATGGTGAGACCCTTTCTCTACTAAAATACAAAAAAAAACA A G LINC01010 Ensembl:ENSG00000236700 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1421844487 Functional Loss SNV dbSNP153 33..33 33 - - - 16890 RMVar_ID_16890 Human_SNP_ID_297497745 A-to-I Human chr6 + 134399392 134399392 134399392 TCTGGGCAACATAGTGAAACCTCATCTCTATTAAAAAAATACAAAACTTAGATGGGTTTGGTGGT TCTGGGCAACATAGTGAAACCTCATCTCTATTTAAAAAATACAAAACTTAGATGGGTTTGGTGGT A T LINC01010 Ensembl:ENSG00000236700 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1326429296 Functional Loss SNV dbSNP153 33..33 33 - - - 16891 RMVar_ID_16891 Human_SNP_ID_297503066 A-to-I Human chr6 - 134419152 134419152 134419152 GAGATGGGCAGATCACCTGAAGTCAGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCCCCA GAGATGGGCAGATCACCTGAAGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCCCA T C lnc-SGK1-5,lnc-SGK1-5:2,lnc-SGK1-5:3 RNACentral:URS0000D570C2,RNACentral:URS0000D594C7,RNACentral:URS0000D599D3 lincRNA,lincRNA,lincRNA exon,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs536001229 Functional Loss SNV dbSNP153 33..33 33 - - - 16892 RMVar_ID_16892 Human_SNP_ID_297638379 A-to-I Human chr6 - 134985589 134985589 134985589 TGCTCAAAAAGTTTCAGATTTTGGAGCATTTCAGATTTCAGAATTTTGGATTTGGGATGCTCAAT TGCTCAAAAAGTTTCAGATTTTGGAGCATTTCGGATTTCAGAATTTTGGATTTGGGATGCTCAAT T C HBS1L Ensembl:ENSG00000112339 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1231003700 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6776,RMVar_hsa_circ_337597,RMVar_hsa_circ_36593,RMVar_hsa_circ_71207,RMVar_hsa_circ_100173,RMVar_hsa_circ_57130,RMVar_hsa_circ_241610,RMVar_hsa_circ_368310,RMVar_hsa_circ_307257,RMVar_hsa_circ_75380,RMVar_hsa_circ_14507,RMVar_hsa_circ_58917,RMVar_hsa_circ_28794,RMVar_hsa_circ_241611,RMVar_hsa_circ_265950,RMVar_hsa_circ_268962,RMVar_hsa_circ_356171 16893 RMVar_ID_16893 Human_SNP_ID_590406611 A-to-I Human chr16 - 16679 16679 16679 GACCTGGGCCAGGTGCCTGAGATTGATGTTCCATCCTACCTGCCTGACCTGCCCGGCATTGCCAA GACCTGGGCCAGGTGCCTGAGATTGATGTTCCGTCCTACCTGCCTGACCTGCCCGGCATTGCCAA T C WASH4P Ensembl:ENSG00000234769 Pseudogene exon GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs575317242 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1652204 16894 RMVar_ID_16894 Human_SNP_ID_590406612 A-to-I Human chr16 - 16679 16679 16679 GACCTGGGCCAGGTGCCTGAGATTGATGTTCCATCCTACCTGCCTGACCTGCCCGGCATTGCCAA GACCTGGGCCAGGTGCCTGAGATTGATGTTCCCTCCTACCTGCCTGACCTGCCCGGCATTGCCAA T G WASH4P Ensembl:ENSG00000234769 Pseudogene exon GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs575317242 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1652204 16895 RMVar_ID_16895 Human_SNP_ID_590407787 A-to-I Human chr16 - 19281 19281 19281 GCCAGGAGTAATCAGGGCAGACCCATTAGGGCACGGGGACTTCTGGATTGTGAAATTGGCTCTCT GCCAGGAGTAATCAGGGCAGACCCATTAGGGCGCGGGGACTTCTGGATTGTGAAATTGGCTCTCT T C Z84723.1 Ensembl:ENSG00000260803 lincRNA intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs796150075 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5576248 16896 RMVar_ID_16896 Human_SNP_ID_590417422 A-to-I Human chr16 - 49204 49204 49204 GAACTCCCGACCTCAGGTGATCTGTTGGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCCTGAG GAACTCCCGACCTCAGGTGATCTGTTGGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCCTGAG T C POLR3K Ensembl:ENSG00000161980 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1482409963 Functional Loss SNV dbSNP153 33..33 33 - - - 16897 RMVar_ID_16897 Human_SNP_ID_590417595 A-to-I Human chr16 - 49799 49799 49799 CCCGTCTCCACTAAAAATACAAAAAGTAGCTGAGCGTGGTGGTGCCTGCCTGTAATCCCAGCTAC CCCGTCTCCACTAAAAATACAAAAAGTAGCTGGGCGTGGTGGTGCCTGCCTGTAATCCCAGCTAC T C POLR3K Ensembl:ENSG00000161980 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1421838918 Functional Loss SNV dbSNP153 33..33 33 - - - 16898 RMVar_ID_16898 Human_SNP_ID_590417830 A-to-I Human chr16 - 50647 50647 50647 GTGGTGGCGCTCGCCTGTAGACCCAACTGCTCAGGAGGCTGAGGTACGAGAATTGCTTGAACCCA GTGGTGGCGCTCGCCTGTAGACCCAACTGCTCGGGAGGCTGAGGTACGAGAATTGCTTGAACCCA T C POLR3K Ensembl:ENSG00000161980 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1299139378 Functional Loss SNV dbSNP153 33..33 33 - - - 16899 RMVar_ID_16899 Human_SNP_ID_590417833 A-to-I Human chr16 - 50654 50654 50654 GCCGGGTGTGGTGGCGCTCGCCTGTAGACCCAACTGCTCAGGAGGCTGAGGTACGAGAATTGCTT GCCGGGTGTGGTGGCGCTCGCCTGTAGACCCAGCTGCTCAGGAGGCTGAGGTACGAGAATTGCTT T C POLR3K Ensembl:ENSG00000161980 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs216589 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_1209,GWAS_ID_1210,GWAS_ID_1211,GWAS_ID_1212,GWAS_ID_1213,GWAS_ID_1214,GWAS_ID_1215,GWAS_ID_1216 16900 RMVar_ID_16900 Human_SNP_ID_590418312 A-to-I Human chr16 - 52236 52236 52236 CACCGCGCTGGCCAGGCTGGTCTCGAACTCCCAACCTCAGGTGATCCGCTTGCCTTGGCCTCCCA CACCGCGCTGGCCAGGCTGGTCTCGAACTCCCGACCTCAGGTGATCCGCTTGCCTTGGCCTCCCA T C POLR3K Ensembl:ENSG00000161980 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1409619907 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12662365 16901 RMVar_ID_16901 Human_SNP_ID_590430355 A-to-I Human chr16 - 86778 86778 86778 GCGGCGCTCCCAGCTGCTCATGCTGTTTGACAAGTTCCGCAGCGTGCTGGTGGTGACCACCCACG GCGGCGCTCCCAGCTGCTCATGCTGTTTGACAGGTTCCGCAGCGTGCTGGTGGTGACCACCCACG T C NPRL3 Ensembl:ENSG00000103148 Protein coding exon GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1567127477 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4350739,Human_RBP_ID_18673191 Human_Splice_Rec_1652426,Human_Splice_Rec_1652454,Human_Splice_Rec_1652476,Human_Splice_Rec_1652502,Human_Splice_Rec_1652524,Human_Splice_Rec_1652544 16902 RMVar_ID_16902 Human_SNP_ID_590430540 A-to-I Human chr16 + 87301 87301 87301 TCACCCAGGCTAGATTGCAGTGGCTCGATCTCAGCTCACTGCAACCTCCCGCCTCCCAGATTCAA TCACCCAGGCTAGATTGCAGTGGCTCGATCTCGGCTCACTGCAACCTCCCGCCTCCCAGATTCAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1312309545 Functional Loss SNV dbSNP153 33..33 33 - - - 16903 RMVar_ID_16903 Human_SNP_ID_590430560 A-to-I Human chr16 - 87385 87385 87385 ACTAAAAAAGAGAGAAATTAGCCAGGTGTGGTAGCGCACTCCTGTAGTCCCAGCTTACCTGGGAA ACTAAAAAAGAGAGAAATTAGCCAGGTGTGGTTGCGCACTCCTGTAGTCCCAGCTTACCTGGGAA T A NPRL3 Ensembl:ENSG00000103148 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1056246726 Functional Loss SNV dbSNP153 33..33 33 - - - 16904 RMVar_ID_16904 Human_SNP_ID_590430561 A-to-I Human chr16 - 87385 87385 87385 ACTAAAAAAGAGAGAAATTAGCCAGGTGTGGTAGCGCACTCCTGTAGTCCCAGCTTACCTGGGAA ACTAAAAAAGAGAGAAATTAGCCAGGTGTGGTGGCGCACTCCTGTAGTCCCAGCTTACCTGGGAA T C NPRL3 Ensembl:ENSG00000103148 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1056246726 Functional Loss SNV dbSNP153 33..33 33 - - - 16905 RMVar_ID_16905 Human_SNP_ID_590432759 A-to-I Human chr16 - 93833 93833 93833 ATTGTGGCCGGGTGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGAAGGCCAAGGTGGGTGGA ATTGTGGCCGGGTGCGGTGGCTCATGCCTGTATTCCCAGCACTTTGGAAGGCCAAGGTGGGTGGA T A NPRL3 Ensembl:ENSG00000103148 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978825801 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_126388 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 16906 RMVar_ID_16906 Human_SNP_ID_590432978 A-to-I Human chr16 - 94666 94666 94666 CTCACTGCAACCCCCACCTCCCAGGTGCAAGCAATCCTCCTGTCTCAGCCTCCAAGTAGCTGGGA CTCACTGCAACCCCCACCTCCCAGGTGCAAGCTATCCTCCTGTCTCAGCCTCCAAGTAGCTGGGA T A NPRL3 Ensembl:ENSG00000103148 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs887044290 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17564513 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 16907 RMVar_ID_16907 Human_SNP_ID_590432979 A-to-I Human chr16 - 94666 94666 94666 CTCACTGCAACCCCCACCTCCCAGGTGCAAGCAATCCTCCTGTCTCAGCCTCCAAGTAGCTGGGA CTCACTGCAACCCCCACCTCCCAGGTGCAAGCGATCCTCCTGTCTCAGCCTCCAAGTAGCTGGGA T C NPRL3 Ensembl:ENSG00000103148 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs887044290 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17564513 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 16908 RMVar_ID_16908 Human_SNP_ID_590433623 A-to-I Human chr16 - 96554 96554 96554 ATCGCACCTTGGCCTCCTAAAGGGCTGGTATTACAGGCATGAGCCACCATGCCCAGCTGTGCCTT ATCGCACCTTGGCCTCCTAAAGGGCTGGTATTGCAGGCATGAGCCACCATGCCCAGCTGTGCCTT T C NPRL3 Ensembl:ENSG00000103148 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1362380178 Functional Loss SNV dbSNP153 33..33 33 - - - 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 16909 RMVar_ID_16909 Human_SNP_ID_590436648 A-to-I Human chr16 - 106445 106445 106445 ATTTTTTTGTGGAAATGGGATTTTGCCATGTTACCCTGGCTGATCTTGAATTCCTGGACTCAAGC ATTTTTTTGTGGAAATGGGATTTTGCCATGTTGCCCTGGCTGATCTTGAATTCCTGGACTCAAGC T C NPRL3 Ensembl:ENSG00000103148 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1387322533 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12673134 RMVar_hsa_circ_23515,RMVar_hsa_circ_41368,RMVar_hsa_circ_18523,RMVar_hsa_circ_340681,RMVar_hsa_circ_31031,RMVar_hsa_circ_15605 16910 RMVar_ID_16910 Human_SNP_ID_590437144 A-to-I Human chr16 - 108205 108205 108205 ATCCCTTGTTCATTCTTCTATCGGGAGATATAAGTCCTTAAACATGGGAGAGTGATTTGTCTTTT ATCCCTTGTTCATTCTTCTATCGGGAGATATACGTCCTTAAACATGGGAGAGTGATTTGTCTTTT T G NPRL3 Ensembl:ENSG00000103148 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913665496 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12674140 RMVar_hsa_circ_23515,RMVar_hsa_circ_41368,RMVar_hsa_circ_18523,RMVar_hsa_circ_340681,RMVar_hsa_circ_31031,RMVar_hsa_circ_15605 16911 RMVar_ID_16911 Human_SNP_ID_590437648 A-to-I Human chr16 - 109889 109889 109889 TCTCCTATGTTTAAGGACTTATATTTCCCAATAGAAGAATGAACAAGGGATCTGAGCAGTGAGCT TCTCCTATGTTTAAGGACTTATATTTCCCAATTGAAGAATGAACAAGGGATCTGAGCAGTGAGCT T A NPRL3 Ensembl:ENSG00000103148 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs868444469 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23515,RMVar_hsa_circ_41368,RMVar_hsa_circ_18523,RMVar_hsa_circ_340681,RMVar_hsa_circ_31031,RMVar_hsa_circ_15605 16912 RMVar_ID_16912 Human_SNP_ID_590437650 A-to-I Human chr16 - 109891 109891 109891 ACTCTCCTATGTTTAAGGACTTATATTTCCCAATAGAAGAATGAACAAGGGATCTGAGCAGTGAG ACTCTCCTATGTTTAAGGACTTATATTTCCCAGTAGAAGAATGAACAAGGGATCTGAGCAGTGAG T C NPRL3 Ensembl:ENSG00000103148 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs999097305 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23515,RMVar_hsa_circ_41368,RMVar_hsa_circ_18523,RMVar_hsa_circ_340681,RMVar_hsa_circ_31031,RMVar_hsa_circ_15605 16913 RMVar_ID_16913 Human_SNP_ID_590437651 A-to-I Human chr16 - 109892 109892 109892 CACTCTCCTATGTTTAAGGACTTATATTTCCCAATAGAAGAATGAACAAGGGATCTGAGCAGTGA CACTCTCCTATGTTTAAGGACTTATATTTCCCGATAGAAGAATGAACAAGGGATCTGAGCAGTGA T C NPRL3 Ensembl:ENSG00000103148 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053807284 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23515,RMVar_hsa_circ_41368,RMVar_hsa_circ_18523,RMVar_hsa_circ_340681,RMVar_hsa_circ_31031,RMVar_hsa_circ_15605 16914 RMVar_ID_16914 Human_SNP_ID_590438184 A-to-I Human chr16 - 111588 111588 111588 AAAATTAGCCGGGCATGGTCATATGTGCCCGTAGTTCCAGCTACTCGGGATGCTGAGGTGGGAGA AAAATTAGCCGGGCATGGTCATATGTGCCCGTCGTTCCAGCTACTCGGGATGCTGAGGTGGGAGA T G NPRL3 Ensembl:ENSG00000103148 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs55892571 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23515,RMVar_hsa_circ_41368,RMVar_hsa_circ_18523,RMVar_hsa_circ_340681,RMVar_hsa_circ_31031,RMVar_hsa_circ_303011,RMVar_hsa_circ_15605,RMVar_hsa_circ_310544,RMVar_hsa_circ_337813 16915 RMVar_ID_16915 Human_SNP_ID_590442372 A-to-I Human chr16 - 126374 126373 126374 TCTTGTTGCCCAGGCTGGGGTGCAATGGCGCAATCTCGGCTCACTGCAACCTCTGCCTCCCAGGT TCTTGTTGCCCAGGCTGGGGTGCAATGGCGCA_TCTCGGCTCACTGCAACCTCTGCCTCCCAGGT AT A NPRL3 Ensembl:ENSG00000103148 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs754643235 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_23515,RMVar_hsa_circ_41368,RMVar_hsa_circ_18523,RMVar_hsa_circ_303011,RMVar_hsa_circ_15605,RMVar_hsa_circ_317098,RMVar_hsa_circ_175284,RMVar_hsa_circ_120298,RMVar_hsa_circ_272620,RMVar_hsa_circ_175285,RMVar_hsa_circ_175286 16916 RMVar_ID_16916 Human_SNP_ID_590442373 A-to-I Human chr16 - 126374 126374 126374 TCTTGTTGCCCAGGCTGGGGTGCAATGGCGCAATCTCGGCTCACTGCAACCTCTGCCTCCCAGGT TCTTGTTGCCCAGGCTGGGGTGCAATGGCGCAGTCTCGGCTCACTGCAACCTCTGCCTCCCAGGT T C NPRL3 Ensembl:ENSG00000103148 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1454531575 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23515,RMVar_hsa_circ_41368,RMVar_hsa_circ_18523,RMVar_hsa_circ_303011,RMVar_hsa_circ_15605,RMVar_hsa_circ_317098,RMVar_hsa_circ_175284,RMVar_hsa_circ_120298,RMVar_hsa_circ_272620,RMVar_hsa_circ_175285,RMVar_hsa_circ_175286 16917 RMVar_ID_16917 Human_SNP_ID_590442374 A-to-I Human chr16 - 126375 126375 126375 TTCTTGTTGCCCAGGCTGGGGTGCAATGGCGCAATCTCGGCTCACTGCAACCTCTGCCTCCCAGG TTCTTGTTGCCCAGGCTGGGGTGCAATGGCGCGATCTCGGCTCACTGCAACCTCTGCCTCCCAGG T C NPRL3 Ensembl:ENSG00000103148 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1021788939 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23515,RMVar_hsa_circ_41368,RMVar_hsa_circ_18523,RMVar_hsa_circ_303011,RMVar_hsa_circ_15605,RMVar_hsa_circ_317098,RMVar_hsa_circ_175284,RMVar_hsa_circ_120298,RMVar_hsa_circ_272620,RMVar_hsa_circ_175285,RMVar_hsa_circ_175286 16918 RMVar_ID_16918 Human_SNP_ID_590442378 A-to-I Human chr16 - 126382 126382 126382 AGTTTCATTCTTGTTGCCCAGGCTGGGGTGCAATGGCGCAATCTCGGCTCACTGCAACCTCTGCC AGTTTCATTCTTGTTGCCCAGGCTGGGGTGCAGTGGCGCAATCTCGGCTCACTGCAACCTCTGCC T C NPRL3 Ensembl:ENSG00000103148 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1309392635 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23515,RMVar_hsa_circ_41368,RMVar_hsa_circ_18523,RMVar_hsa_circ_303011,RMVar_hsa_circ_15605,RMVar_hsa_circ_317098,RMVar_hsa_circ_175284,RMVar_hsa_circ_120298,RMVar_hsa_circ_272620,RMVar_hsa_circ_175285,RMVar_hsa_circ_175286 16919 RMVar_ID_16919 Human_SNP_ID_590442684 A-to-I Human chr16 - 127374 127374 127374 AAAAATTAGCTGGGTTGGTGACCTGCGCCCTTAGTCCCAGCCACTGCGGAGGCTGAGGGAGCCCA AAAAATTAGCTGGGTTGGTGACCTGCGCCCTTCGTCCCAGCCACTGCGGAGGCTGAGGGAGCCCA T G NPRL3 Ensembl:ENSG00000103148 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs570765671 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23515,RMVar_hsa_circ_41368,RMVar_hsa_circ_18523,RMVar_hsa_circ_303011,RMVar_hsa_circ_15605,RMVar_hsa_circ_317098,RMVar_hsa_circ_175284,RMVar_hsa_circ_120298,RMVar_hsa_circ_272620,RMVar_hsa_circ_175285,RMVar_hsa_circ_175286 16920 RMVar_ID_16920 Human_SNP_ID_590445327 A-to-I Human chr16 - 135424 135424 135424 TTGTATTTTTAGTAGAGATGGGGTTTCACCATATCAGCCAGGCTGGTCTTGAACTCCTGACCTCG TTGTATTTTTAGTAGAGATGGGGTTTCACCATGTCAGCCAGGCTGGTCTTGAACTCCTGACCTCG T C NPRL3 Ensembl:ENSG00000103148 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1369820484 Functional Loss SNV dbSNP153 33..33 33 - - - 16921 RMVar_ID_16921 Human_SNP_ID_590446076 A-to-I Human chr16 - 137726 137726 137726 AACTCTGTCTCTACTGAAAAAATAAAAATAAAAAAAAACAAATTAGCCGAGCGTGGTGGTGCGTG AACTCTGTCTCTACTGAAAAAATAAAAATAAATAAAAACAAATTAGCCGAGCGTGGTGGTGCGTG T A NPRL3 Ensembl:ENSG00000103148 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1011663706 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25242389 16922 RMVar_ID_16922 Human_SNP_ID_590446077 A-to-I Human chr16 - 137726 137726 137726 AACTCTGTCTCTACTGAAAAAATAAAAATAAAAAAAAACAAATTAGCCGAGCGTGGTGGTGCGTG AACTCTGTCTCTACTGAAAAAATAAAAATAAACAAAAACAAATTAGCCGAGCGTGGTGGTGCGTG T G NPRL3 Ensembl:ENSG00000103148 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1011663706 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25242389 16923 RMVar_ID_16923 Human_SNP_ID_590467185 A-to-I Human chr16 - 198034 198034 198034 TCGATCTCCTGACCTCGCGATCCGCCCGCCTCAGCCTCCCAAAGTGCTGGGACCACAGGCGTGAG TCGATCTCCTGACCTCGCGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGACCACAGGCGTGAG T C LUC7L Ensembl:ENSG00000007392 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1481760577 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27658,RMVar_hsa_circ_63159,RMVar_hsa_circ_175293,RMVar_hsa_circ_175295,RMVar_hsa_circ_313209,RMVar_hsa_circ_351143,RMVar_hsa_circ_311902,RMVar_hsa_circ_175294 16924 RMVar_ID_16924 Human_SNP_ID_590467217 A-to-I Human chr16 - 198101 198101 198101 CTAATTTTTGTTGTTGTTGTTGTATTTTTAGTAGAGACGGGGCTTCATCGTGTTTGCCAGGATGG CTAATTTTTGTTGTTGTTGTTGTATTTTTAGTGGAGACGGGGCTTCATCGTGTTTGCCAGGATGG T C LUC7L Ensembl:ENSG00000007392 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs570667072 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12700637 RMVar_hsa_circ_27658,RMVar_hsa_circ_63159,RMVar_hsa_circ_175293,RMVar_hsa_circ_175295,RMVar_hsa_circ_313209,RMVar_hsa_circ_351143,RMVar_hsa_circ_311902,RMVar_hsa_circ_175294 16925 RMVar_ID_16925 Human_SNP_ID_590467368 A-to-I Human chr16 - 198419 198419 198419 GACAGAGTGTCACACATCCTGGCTCCTTGCCTATGAGCCACCTCAGAAGGGCGGGGTGAAGATGG GACAGAGTGTCACACATCCTGGCTCCTTGCCTGTGAGCCACCTCAGAAGGGCGGGGTGAAGATGG T C LUC7L Ensembl:ENSG00000007392 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2685123 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27658,RMVar_hsa_circ_63159,RMVar_hsa_circ_175293,RMVar_hsa_circ_175295,RMVar_hsa_circ_313209,RMVar_hsa_circ_351143,RMVar_hsa_circ_311902,RMVar_hsa_circ_175294 16926 RMVar_ID_16926 Human_SNP_ID_590468248 A-to-I Human chr16 - 201021 201021 201021 GGATTACAGGTGCCAGCCACCGTGCCCAGCTAATTTTTTTGTATTTTTAATAGAGACGGGGTTTC GGATTACAGGTGCCAGCCACCGTGCCCAGCTACTTTTTTTGTATTTTTAATAGAGACGGGGTTTC T G LUC7L Ensembl:ENSG00000007392 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs140924333 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27658,RMVar_hsa_circ_63159,RMVar_hsa_circ_175299,RMVar_hsa_circ_175295,RMVar_hsa_circ_313209,RMVar_hsa_circ_351143,RMVar_hsa_circ_175294,RMVar_hsa_circ_49094,RMVar_hsa_circ_276591,RMVar_hsa_circ_300965,RMVar_hsa_circ_272562,RMVar_hsa_circ_175297,RMVar_hsa_circ_175298,RMVar_hsa_circ_175296 16927 RMVar_ID_16927 Human_SNP_ID_590468468 A-to-I Human chr16 - 201525 201525 201525 TGAGGCAGGTGAATGGTGTGGACCCGGGAGGCAGAGCTTGTAGTGAGCTGAGATCGTGCCACTGC TGAGGCAGGTGAATGGTGTGGACCCGGGAGGCGGAGCTTGTAGTGAGCTGAGATCGTGCCACTGC T C LUC7L Ensembl:ENSG00000007392 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1473432518 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6503966 RMVar_hsa_circ_27658,RMVar_hsa_circ_63159,RMVar_hsa_circ_175299,RMVar_hsa_circ_175295,RMVar_hsa_circ_313209,RMVar_hsa_circ_351143,RMVar_hsa_circ_175294,RMVar_hsa_circ_49094,RMVar_hsa_circ_276591,RMVar_hsa_circ_300965,RMVar_hsa_circ_272562,RMVar_hsa_circ_175297,RMVar_hsa_circ_175298,RMVar_hsa_circ_175296 16928 RMVar_ID_16928 Human_SNP_ID_590468506 A-to-I Human chr16 - 201620 201620 201620 CCTGGCTAACATGGTGATACTCCGTCTCTACTAAAAATACAAAAAATTGGCCGGGCGTGGCGGCG CCTGGCTAACATGGTGATACTCCGTCTCTACTGAAAATACAAAAAATTGGCCGGGCGTGGCGGCG T C LUC7L Ensembl:ENSG00000007392 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs981810653 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27658,RMVar_hsa_circ_63159,RMVar_hsa_circ_175299,RMVar_hsa_circ_175295,RMVar_hsa_circ_313209,RMVar_hsa_circ_351143,RMVar_hsa_circ_175294,RMVar_hsa_circ_49094,RMVar_hsa_circ_276591,RMVar_hsa_circ_300965,RMVar_hsa_circ_272562,RMVar_hsa_circ_175297,RMVar_hsa_circ_175298,RMVar_hsa_circ_175296 16929 RMVar_ID_16929 Human_SNP_ID_590469850 A-to-I Human chr16 - 205701 205700 205702 CCTGTAGTCCCAGCTGCTCCGGAGGCTGAGGAAGGAGAATGGCGTGAACCCGGGAGGCGGAGCTT CCTGTAGTCCCAGCTGCTCCGGAGGCTGAGG__GGAGAATGGCGTGAACCCGGGAGGCGGAGCTT CTT C LUC7L Ensembl:ENSG00000007392 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215624431 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_27658,RMVar_hsa_circ_63159,RMVar_hsa_circ_175299,RMVar_hsa_circ_175295,RMVar_hsa_circ_313209,RMVar_hsa_circ_351143,RMVar_hsa_circ_175294,RMVar_hsa_circ_49094,RMVar_hsa_circ_276591,RMVar_hsa_circ_300965,RMVar_hsa_circ_272562,RMVar_hsa_circ_175297,RMVar_hsa_circ_175298,RMVar_hsa_circ_175296 16930 RMVar_ID_16930 Human_SNP_ID_590470358 A-to-I Human chr16 - 207401 207401 207401 CCTGAGCAACATGAAGAAACCCCATCTCTACAAAAAATACATATATTAGCCAGGCTTGGTGGTGC CCTGAGCAACATGAAGAAACCCCATCTCTACAGAAAATACATATATTAGCCAGGCTTGGTGGTGC T C LUC7L Ensembl:ENSG00000007392 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1185116760 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27658,RMVar_hsa_circ_63159,RMVar_hsa_circ_79555,RMVar_hsa_circ_175295,RMVar_hsa_circ_313209,RMVar_hsa_circ_351143,RMVar_hsa_circ_175294,RMVar_hsa_circ_49094,RMVar_hsa_circ_276591,RMVar_hsa_circ_272562,RMVar_hsa_circ_175297,RMVar_hsa_circ_175298,RMVar_hsa_circ_302118,RMVar_hsa_circ_175296,RMVar_hsa_circ_274392,RMVar_hsa_circ_175301,RMVar_hsa_circ_175302,RMVar_hsa_circ_175303 16931 RMVar_ID_16931 Human_SNP_ID_590470859 A-to-I Human chr16 - 209124 209124 209124 GCTGGAGTGTGGTGGTCTGGTCTCAGTTCACTACAACTTCTGCCTCCGAGGCTCAAGCGATTCTC GCTGGAGTGTGGTGGTCTGGTCTCAGTTCACTGCAACTTCTGCCTCCGAGGCTCAAGCGATTCTC T C LUC7L Ensembl:ENSG00000007392 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1214580142 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12704429 RMVar_hsa_circ_79555,RMVar_hsa_circ_175295,RMVar_hsa_circ_313209,RMVar_hsa_circ_272562,RMVar_hsa_circ_175297,RMVar_hsa_circ_302118,RMVar_hsa_circ_175296,RMVar_hsa_circ_23776,RMVar_hsa_circ_175302,RMVar_hsa_circ_175303,RMVar_hsa_circ_315732,RMVar_hsa_circ_333586 16932 RMVar_ID_16932 Human_SNP_ID_590471492 A-to-I Human chr16 - 211382 211382 211382 GTGATCTTGGCTCACTGCAACCTCCGCCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCT GTGATCTTGGCTCACTGCAACCTCCGCCTCCCTGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCT T A LUC7L Ensembl:ENSG00000007392 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1026063450 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79555,RMVar_hsa_circ_175295,RMVar_hsa_circ_313209,RMVar_hsa_circ_272562,RMVar_hsa_circ_175297,RMVar_hsa_circ_302118,RMVar_hsa_circ_175296,RMVar_hsa_circ_23776,RMVar_hsa_circ_175302,RMVar_hsa_circ_175303,RMVar_hsa_circ_315732,RMVar_hsa_circ_333586 16933 RMVar_ID_16933 Human_SNP_ID_590471493 A-to-I Human chr16 - 211382 211382 211382 GTGATCTTGGCTCACTGCAACCTCCGCCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCT GTGATCTTGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCT T C LUC7L Ensembl:ENSG00000007392 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1026063450 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79555,RMVar_hsa_circ_175295,RMVar_hsa_circ_313209,RMVar_hsa_circ_272562,RMVar_hsa_circ_175297,RMVar_hsa_circ_302118,RMVar_hsa_circ_175296,RMVar_hsa_circ_23776,RMVar_hsa_circ_175302,RMVar_hsa_circ_175303,RMVar_hsa_circ_315732,RMVar_hsa_circ_333586 16934 RMVar_ID_16934 Human_SNP_ID_590471899 A-to-I Human chr16 - 212835 212835 212835 AGGTCAACGCTAAAGTGAGCCGTGATCGTGCCACTGTATTCTAGCCTGGGTGACAGAGCAAGATC AGGTCAACGCTAAAGTGAGCCGTGATCGTGCCTCTGTATTCTAGCCTGGGTGACAGAGCAAGATC T A LUC7L Ensembl:ENSG00000007392 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,cerebellum - 29129909,30559470 RNA-Seq:(High) rs1265350918 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79555,RMVar_hsa_circ_175295,RMVar_hsa_circ_313209,RMVar_hsa_circ_272562,RMVar_hsa_circ_175297,RMVar_hsa_circ_302118,RMVar_hsa_circ_175296,RMVar_hsa_circ_23776,RMVar_hsa_circ_175302,RMVar_hsa_circ_175303,RMVar_hsa_circ_315732,RMVar_hsa_circ_333586 16935 RMVar_ID_16935 Human_SNP_ID_590471918 A-to-I Human chr16 - 212918 212918 212918 GAAATGTTAGCTGGGTGTAGTGACGTGTTCCTATAGTCCTACCTGCTTTGGAGGCTGAGGTGGAA GAAATGTTAGCTGGGTGTAGTGACGTGTTCCTGTAGTCCTACCTGCTTTGGAGGCTGAGGTGGAA T C LUC7L Ensembl:ENSG00000007392 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs116208446 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17563900,Human_RBP_ID_20108515 RMVar_hsa_circ_79555,RMVar_hsa_circ_175295,RMVar_hsa_circ_313209,RMVar_hsa_circ_272562,RMVar_hsa_circ_175297,RMVar_hsa_circ_302118,RMVar_hsa_circ_175296,RMVar_hsa_circ_23776,RMVar_hsa_circ_175302,RMVar_hsa_circ_175303,RMVar_hsa_circ_315732,RMVar_hsa_circ_333586 16936 RMVar_ID_16936 Human_SNP_ID_590472101 A-to-I Human chr16 - 213608 213608 213608 ATGAGGTCAGGAGTTCGAGACCAGTCTGACCAACATGGTGATAACCTGTCTCTAATAAAAATACA ATGAGGTCAGGAGTTCGAGACCAGTCTGACCAGCATGGTGATAACCTGTCTCTAATAAAAATACA T C LUC7L Ensembl:ENSG00000007392 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1181896791 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79555,RMVar_hsa_circ_175295,RMVar_hsa_circ_313209,RMVar_hsa_circ_272562,RMVar_hsa_circ_175297,RMVar_hsa_circ_302118,RMVar_hsa_circ_175296,RMVar_hsa_circ_23776,RMVar_hsa_circ_175302,RMVar_hsa_circ_175303,RMVar_hsa_circ_315732,RMVar_hsa_circ_333586 16937 RMVar_ID_16937 Human_SNP_ID_590472192 A-to-I Human chr16 - 213915 213915 213915 GATCAGGAGATGGAGACCTTCCTGGCCAAGATAGTGAGACCCCATCTCTACTAAAAATAGAAAAT GATCAGGAGATGGAGACCTTCCTGGCCAAGATGGTGAGACCCCATCTCTACTAAAAATAGAAAAT T C LUC7L Ensembl:ENSG00000007392 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1204782727 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25201440 RMVar_hsa_circ_79555,RMVar_hsa_circ_175295,RMVar_hsa_circ_313209,RMVar_hsa_circ_272562,RMVar_hsa_circ_175297,RMVar_hsa_circ_302118,RMVar_hsa_circ_175296,RMVar_hsa_circ_23776,RMVar_hsa_circ_175302,RMVar_hsa_circ_175303,RMVar_hsa_circ_315732,RMVar_hsa_circ_333586 16938 RMVar_ID_16938 Human_SNP_ID_590472623 A-to-I Human chr16 - 215471 215471 215471 GGATTGCAGGCACGCGCCACCATGCCTGGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTTA GGATTGCAGGCACGCGCCACCATGCCTGGCTACTTTTTTGTATTTTTAGTAGAGACGGGGTTTTA T G LUC7L Ensembl:ENSG00000007392 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs993022623 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25201486 RMVar_hsa_circ_79555,RMVar_hsa_circ_175295,RMVar_hsa_circ_313209,RMVar_hsa_circ_272562,RMVar_hsa_circ_175297,RMVar_hsa_circ_302118,RMVar_hsa_circ_175296,RMVar_hsa_circ_23776,RMVar_hsa_circ_175302,RMVar_hsa_circ_175303,RMVar_hsa_circ_315732,RMVar_hsa_circ_333586 16939 RMVar_ID_16939 Human_SNP_ID_590472649 A-to-I Human chr16 - 215534 215534 215534 CTCACTGCAACCTCCGCCTGCCGGGTTCAAGCAACTCTCCTACCTCAGCCTCCCAAGTAGCTGGG CTCACTGCAACCTCCGCCTGCCGGGTTCAAGCGACTCTCCTACCTCAGCCTCCCAAGTAGCTGGG T C LUC7L Ensembl:ENSG00000007392 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs944006621 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5182322,Human_RBP_ID_25201487 RMVar_hsa_circ_79555,RMVar_hsa_circ_175295,RMVar_hsa_circ_313209,RMVar_hsa_circ_272562,RMVar_hsa_circ_175297,RMVar_hsa_circ_302118,RMVar_hsa_circ_175296,RMVar_hsa_circ_23776,RMVar_hsa_circ_175302,RMVar_hsa_circ_175303,RMVar_hsa_circ_315732,RMVar_hsa_circ_333586 16940 RMVar_ID_16940 Human_SNP_ID_590472807 A-to-I Human chr16 - 216036 216035 216037 GATCGTGCCATTGCACTGTAGCCTGGGCAACAAGAGCGAAATCCCATCTCAAAAAAAAAACAGTA GATCGTGCCATTGCACTGTAGCCTGGGCAAC__GAGCGAAATCCCATCTCAAAAAAAAAACAGTA CTT C LUC7L Ensembl:ENSG00000007392 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1238118107 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_12705086,Human_RBP_ID_25201504 RMVar_hsa_circ_79555,RMVar_hsa_circ_175295,RMVar_hsa_circ_313209,RMVar_hsa_circ_272562,RMVar_hsa_circ_175297,RMVar_hsa_circ_302118,RMVar_hsa_circ_175296,RMVar_hsa_circ_23776,RMVar_hsa_circ_175302,RMVar_hsa_circ_175303,RMVar_hsa_circ_315732,RMVar_hsa_circ_333586 16941 RMVar_ID_16941 Human_SNP_ID_590472825 A-to-I Human chr16 - 216113 216113 216113 CCTATAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCTGGGAGGCAGAGGTT CCTATAATCCCAGCTACTCGGGAGGCTGAGGCGGGAGAATCACTTGAACCTGGGAGGCAGAGGTT T C LUC7L Ensembl:ENSG00000007392 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1334318229 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79555,RMVar_hsa_circ_175295,RMVar_hsa_circ_313209,RMVar_hsa_circ_272562,RMVar_hsa_circ_175297,RMVar_hsa_circ_302118,RMVar_hsa_circ_175296,RMVar_hsa_circ_23776,RMVar_hsa_circ_175302,RMVar_hsa_circ_175303,RMVar_hsa_circ_315732,RMVar_hsa_circ_333586 16942 RMVar_ID_16942 Human_SNP_ID_590472858 A-to-I Human chr16 - 216176 216176 216176 CCATCATGGAGAAACCCCCATCTCTATTAAAAATTGAAAATTAGCCGGGCGTGGTGCTGGGCACC CCATCATGGAGAAACCCCCATCTCTATTAAAAGTTGAAAATTAGCCGGGCGTGGTGCTGGGCACC T C LUC7L Ensembl:ENSG00000007392 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1353808772 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79555,RMVar_hsa_circ_175295,RMVar_hsa_circ_313209,RMVar_hsa_circ_272562,RMVar_hsa_circ_175297,RMVar_hsa_circ_302118,RMVar_hsa_circ_175296,RMVar_hsa_circ_23776,RMVar_hsa_circ_175302,RMVar_hsa_circ_175303,RMVar_hsa_circ_315732,RMVar_hsa_circ_333586 16943 RMVar_ID_16943 Human_SNP_ID_590473177 A-to-I Human chr16 - 217048 217048 217048 CACACCATTGCACTTTATTCTACTTGGGTGACAGAGCGAAACTCTGTCTCAAAAAAAAAAATTCT CACACCATTGCACTTTATTCTACTTGGGTGACGGAGCGAAACTCTGTCTCAAAAAAAAAAATTCT T C LUC7L Ensembl:ENSG00000007392 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1227259750 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17564522 RMVar_hsa_circ_79555,RMVar_hsa_circ_175295,RMVar_hsa_circ_313209,RMVar_hsa_circ_272562,RMVar_hsa_circ_175297,RMVar_hsa_circ_302118,RMVar_hsa_circ_175296,RMVar_hsa_circ_23776,RMVar_hsa_circ_175302,RMVar_hsa_circ_175303,RMVar_hsa_circ_315732,RMVar_hsa_circ_333586 16944 RMVar_ID_16944 Human_SNP_ID_590473200 A-to-I Human chr16 - 217148 217148 217148 GCTGGGCATGGTGGTGCTGTCCTCTAATCCCAACTACTCGGGAGACTGAGGCAGGAGAATGGCTT GCTGGGCATGGTGGTGCTGTCCTCTAATCCCAGCTACTCGGGAGACTGAGGCAGGAGAATGGCTT T C LUC7L Ensembl:ENSG00000007392 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs544911150 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17563902,Human_RBP_ID_22715194 RMVar_hsa_circ_79555,RMVar_hsa_circ_175295,RMVar_hsa_circ_313209,RMVar_hsa_circ_272562,RMVar_hsa_circ_175297,RMVar_hsa_circ_302118,RMVar_hsa_circ_175296,RMVar_hsa_circ_23776,RMVar_hsa_circ_175302,RMVar_hsa_circ_175303,RMVar_hsa_circ_315732,RMVar_hsa_circ_333586 16945 RMVar_ID_16945 Human_SNP_ID_590473228 A-to-I Human chr16 - 217236 217236 217236 GAGGTGGGTGGATCACCTGAGGTCGGGAGTTGAAGACTAGCCTGGCCAACATGGTGAAACGCTGC GAGGTGGGTGGATCACCTGAGGTCGGGAGTTGGAGACTAGCCTGGCCAACATGGTGAAACGCTGC T C LUC7L Ensembl:ENSG00000007392 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1286779293 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79555,RMVar_hsa_circ_175295,RMVar_hsa_circ_313209,RMVar_hsa_circ_272562,RMVar_hsa_circ_175297,RMVar_hsa_circ_302118,RMVar_hsa_circ_175296,RMVar_hsa_circ_23776,RMVar_hsa_circ_175302,RMVar_hsa_circ_175303,RMVar_hsa_circ_315732,RMVar_hsa_circ_333586 16946 RMVar_ID_16946 Human_SNP_ID_590473306 A-to-I Human chr16 - 217504 217504 217504 CGGGGTTTTGTCATGTTGGCCAGGCTGGTCTTAAACTCCTGACCGCAGGTGATCCACCCGCCTTA CGGGGTTTTGTCATGTTGGCCAGGCTGGTCTTGAACTCCTGACCGCAGGTGATCCACCCGCCTTA T C LUC7L Ensembl:ENSG00000007392 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1420832366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12705148 RMVar_hsa_circ_79555,RMVar_hsa_circ_175295,RMVar_hsa_circ_313209,RMVar_hsa_circ_272562,RMVar_hsa_circ_175297,RMVar_hsa_circ_302118,RMVar_hsa_circ_175296,RMVar_hsa_circ_23776,RMVar_hsa_circ_175302,RMVar_hsa_circ_175303,RMVar_hsa_circ_315732,RMVar_hsa_circ_333586 16947 RMVar_ID_16947 Human_SNP_ID_590473444 A-to-I Human chr16 - 217876 217876 217876 CGCCACCACGCCCAGCTAATTTTTATATTTTTAGTAGAGATGAGGTTTCACCATTTTGGTCAGGC CGCCACCACGCCCAGCTAATTTTTATATTTTTGGTAGAGATGAGGTTTCACCATTTTGGTCAGGC T C LUC7L Ensembl:ENSG00000007392 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs538409826 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12705164 RMVar_hsa_circ_79555,RMVar_hsa_circ_175295,RMVar_hsa_circ_313209,RMVar_hsa_circ_272562,RMVar_hsa_circ_175297,RMVar_hsa_circ_302118,RMVar_hsa_circ_175296,RMVar_hsa_circ_23776,RMVar_hsa_circ_175302,RMVar_hsa_circ_175303,RMVar_hsa_circ_315732,RMVar_hsa_circ_333586 16948 RMVar_ID_16948 Human_SNP_ID_590473695 A-to-I Human chr16 - 218558 218558 218558 CGCCACCACACCCAGCTGATTTTTGTATTTTTAGTAGAGATGTGGTTTCGCCATGTTGGCCAGGC CGCCACCACACCCAGCTGATTTTTGTATTTTTGGTAGAGATGTGGTTTCGCCATGTTGGCCAGGC T C LUC7L Ensembl:ENSG00000007392 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1255790148 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79555,RMVar_hsa_circ_175295,RMVar_hsa_circ_313209,RMVar_hsa_circ_272562,RMVar_hsa_circ_175297,RMVar_hsa_circ_302118,RMVar_hsa_circ_175296,RMVar_hsa_circ_23776,RMVar_hsa_circ_175302,RMVar_hsa_circ_175303,RMVar_hsa_circ_315732,RMVar_hsa_circ_333586 16949 RMVar_ID_16949 Human_SNP_ID_590473726 A-to-I Human chr16 - 218674 218674 218674 CTCTGTTGCCCAAGCTGGAATGCAGTGGCGCAATCTTGGCTCATTGCAACCTCCGCCTCCTGGGT CTCTGTTGCCCAAGCTGGAATGCAGTGGCGCAGTCTTGGCTCATTGCAACCTCCGCCTCCTGGGT T C LUC7L Ensembl:ENSG00000007392 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs896537242 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12705198 RMVar_hsa_circ_79555,RMVar_hsa_circ_175295,RMVar_hsa_circ_313209,RMVar_hsa_circ_272562,RMVar_hsa_circ_175297,RMVar_hsa_circ_302118,RMVar_hsa_circ_175296,RMVar_hsa_circ_23776,RMVar_hsa_circ_175302,RMVar_hsa_circ_175303,RMVar_hsa_circ_315732,RMVar_hsa_circ_333586 16950 RMVar_ID_16950 Human_SNP_ID_590474040 A-to-I Human chr16 - 219638 219638 219638 GAACTCTCAACGTCAGGTGATCCGCCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTTGAGC GAACTCTCAACGTCAGGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTTGAGC T C LUC7L Ensembl:ENSG00000007392 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1405680220 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79555,RMVar_hsa_circ_175295,RMVar_hsa_circ_313209,RMVar_hsa_circ_272562,RMVar_hsa_circ_175297,RMVar_hsa_circ_302118,RMVar_hsa_circ_175296,RMVar_hsa_circ_23776,RMVar_hsa_circ_175302,RMVar_hsa_circ_175303,RMVar_hsa_circ_315732,RMVar_hsa_circ_333586 16951 RMVar_ID_16951 Human_SNP_ID_590474678 A-to-I Human chr16 - 221603 221603 221603 CACCTCCTGGGTTCAAGCGATTCTTGTGTCTCAGCTCCCCAGGTAGCTGGGATTACAGGTGCCCT CACCTCCTGGGTTCAAGCGATTCTTGTGTCTCTGCTCCCCAGGTAGCTGGGATTACAGGTGCCCT T A LUC7L Ensembl:ENSG00000007392 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs770249692 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79555,RMVar_hsa_circ_175295,RMVar_hsa_circ_313209,RMVar_hsa_circ_175296,RMVar_hsa_circ_23776,RMVar_hsa_circ_175303,RMVar_hsa_circ_333586,RMVar_hsa_circ_335219,RMVar_hsa_circ_345851 16952 RMVar_ID_16952 Human_SNP_ID_590474686 A-to-I Human chr16 - 221620 221620 221620 TGGCTCACTGCAAACTCCACCTCCTGGGTTCAAGCGATTCTTGTGTCTCAGCTCCCCAGGTAGCT TGGCTCACTGCAAACTCCACCTCCTGGGTTCAGGCGATTCTTGTGTCTCAGCTCCCCAGGTAGCT T C LUC7L Ensembl:ENSG00000007392 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs889588208 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79555,RMVar_hsa_circ_175295,RMVar_hsa_circ_313209,RMVar_hsa_circ_175296,RMVar_hsa_circ_23776,RMVar_hsa_circ_175303,RMVar_hsa_circ_333586,RMVar_hsa_circ_335219,RMVar_hsa_circ_345851 16953 RMVar_ID_16953 Human_SNP_ID_590475831 A-to-I Human chr16 - 224786 224786 224786 ACTCTGTTGCCTAGGCTGGAGTGCATGGTGCTATCTCTGCTCACTGCAACCTCTGTCTCCTGGGT ACTCTGTTGCCTAGGCTGGAGTGCATGGTGCTGTCTCTGCTCACTGCAACCTCTGTCTCCTGGGT T C LUC7L Ensembl:ENSG00000007392 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1255286338 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12705994 RMVar_hsa_circ_79555,RMVar_hsa_circ_175295,RMVar_hsa_circ_313209,RMVar_hsa_circ_175296,RMVar_hsa_circ_23776,RMVar_hsa_circ_175303,RMVar_hsa_circ_333586,RMVar_hsa_circ_335219,RMVar_hsa_circ_345851 16954 RMVar_ID_16954 Human_SNP_ID_590475975 A-to-I Human chr16 - 225318 225318 225318 CCTCGCCCGGCTAACTTTTGTATTTTCAGTAGAGACGGGGTTTCACCATGTTGACCAGGCTAGTC CCTCGCCCGGCTAACTTTTGTATTTTCAGTAGGGACGGGGTTTCACCATGTTGACCAGGCTAGTC T C LUC7L Ensembl:ENSG00000007392 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1433206803 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79555,RMVar_hsa_circ_175295,RMVar_hsa_circ_313209,RMVar_hsa_circ_175296,RMVar_hsa_circ_23776,RMVar_hsa_circ_175303,RMVar_hsa_circ_333586,RMVar_hsa_circ_335219,RMVar_hsa_circ_345851 16955 RMVar_ID_16955 Human_SNP_ID_590475976 A-to-I Human chr16 - 225320 225320 225320 CACCTCGCCCGGCTAACTTTTGTATTTTCAGTAGAGACGGGGTTTCACCATGTTGACCAGGCTAG CACCTCGCCCGGCTAACTTTTGTATTTTCAGTGGAGACGGGGTTTCACCATGTTGACCAGGCTAG T C LUC7L Ensembl:ENSG00000007392 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs753942155 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79555,RMVar_hsa_circ_175295,RMVar_hsa_circ_313209,RMVar_hsa_circ_175296,RMVar_hsa_circ_23776,RMVar_hsa_circ_175303,RMVar_hsa_circ_333586,RMVar_hsa_circ_335219,RMVar_hsa_circ_345851 16956 RMVar_ID_16956 Human_SNP_ID_590475993 A-to-I Human chr16 - 225374 225369 225375 TCAAGCCATTCTCTTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCATGCACCACCTCGCCCG TCAAGCCATTCTCTTGCCTCAGCCTCCCGAG______GGATTACAGGCATGCACCACCTCGCCCG CCAGCTA C LUC7L Ensembl:ENSG00000007392 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1430175990 Functional Loss DEL dbSNP153 32..37 33 - - - RMVar_hsa_circ_79555,RMVar_hsa_circ_175295,RMVar_hsa_circ_313209,RMVar_hsa_circ_175296,RMVar_hsa_circ_23776,RMVar_hsa_circ_175303,RMVar_hsa_circ_333586,RMVar_hsa_circ_335219,RMVar_hsa_circ_345851 16957 RMVar_ID_16957 Human_SNP_ID_590476098 A-to-I Human chr16 - 225611 225611 225611 GTGGTGGCGCATGCCTGTAATCCCAGCTACTCAGGAGACTGAGGCAGGAGAGTCACTTGAACCCG GTGGTGGCGCATGCCTGTAATCCCAGCTACTCGGGAGACTGAGGCAGGAGAGTCACTTGAACCCG T C LUC7L Ensembl:ENSG00000007392 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7200874 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_1217,GWAS_ID_1218,GWAS_ID_1219,GWAS_ID_1220,GWAS_ID_1221,GWAS_ID_1222,GWAS_ID_1223,GWAS_ID_1224,GWAS_ID_1225,GWAS_ID_1226,GWAS_ID_1227,GWAS_ID_1228,GWAS_ID_1229 RMVar_hsa_circ_79555,RMVar_hsa_circ_175295,RMVar_hsa_circ_313209,RMVar_hsa_circ_175296,RMVar_hsa_circ_23776,RMVar_hsa_circ_175303,RMVar_hsa_circ_333586,RMVar_hsa_circ_335219,RMVar_hsa_circ_345851 16958 RMVar_ID_16958 Human_SNP_ID_590480472 A-to-I Human chr16 + 238219 238219 238219 TTTTGTGTTTTTGGTAGAGACGAGGTTTCGCCATGTTGGCCAGGCTGGTCTTGAACTCCTGATGT TTTTGTGTTTTTGGTAGAGACGAGGTTTCGCCGTGTTGGCCAGGCTGGTCTTGAACTCCTGATGT A G FAM234A Ensembl:ENSG00000167930 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1399638624 Functional Loss SNV dbSNP153 33..33 33 - - - 16959 RMVar_ID_16959 Human_SNP_ID_590482249 A-to-I Human chr16 + 243247 243247 243247 GTCATCCTCCTGCCTCAGCCTCCCAAAGCACTAGGATTATAGGCGTGAACCACCCTGCCCGGCCA GTCATCCTCCTGCCTCAGCCTCCCAAAGCACTGGGATTATAGGCGTGAACCACCCTGCCCGGCCA A G FAM234A Ensembl:ENSG00000167930 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1567208922 Functional Loss SNV dbSNP153 33..33 33 - - - 16960 RMVar_ID_16960 Human_SNP_ID_590483184 A-to-I Human chr16 + 245982 245982 245982 TAATCCCAGCACTTTGAGAGGCTTAGGTGGGCAGATCACGAGGTCAGCAGTTCTAGACCAGCCTG TAATCCCAGCACTTTGAGAGGCTTAGGTGGGCTGATCACGAGGTCAGCAGTTCTAGACCAGCCTG A T FAM234A Ensembl:ENSG00000167930 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1221618612 Functional Loss SNV dbSNP153 33..33 33 - - - 16961 RMVar_ID_16961 Human_SNP_ID_590505808 A-to-I Human chr16 - 301606 301606 301606 AAAATATTTTTGTAGAGATGGAATCTTGCTATATTACCCACACTGGTCTTGAACTCCTGGCCTCA AAAATATTTTTGTAGAGATGGAATCTTGCTATGTTACCCACACTGGTCTTGAACTCCTGGCCTCA T C AXIN1 Ensembl:ENSG00000103126 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1230022110 Functional Loss SNV dbSNP153 33..33 33 - - - 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 16962 RMVar_ID_16962 Human_SNP_ID_590509624 A-to-I Human chr16 - 313263 313263 313263 CAGGATCTCACTGTCACCCAGGCTGGACTGCAATGGTGCGATCTTGGCTTACTGTAGCTTCTGTC CAGGATCTCACTGTCACCCAGGCTGGACTGCAGTGGTGCGATCTTGGCTTACTGTAGCTTCTGTC T C AXIN1 Ensembl:ENSG00000103126 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs967758957 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12729574 RMVar_hsa_circ_85828,RMVar_hsa_circ_175316,RMVar_hsa_circ_117231,RMVar_hsa_circ_175318,RMVar_hsa_circ_106435,RMVar_hsa_circ_175319,RMVar_hsa_circ_289861,RMVar_hsa_circ_270418,RMVar_hsa_circ_175323,RMVar_hsa_circ_175324,RMVar_hsa_circ_307633,RMVar_hsa_circ_290683,RMVar_hsa_circ_175326,RMVar_hsa_circ_175327 16963 RMVar_ID_16963 Human_SNP_ID_590521427 A-to-I Human chr16 - 348565 348565 348565 GAACTCTTGGGCTCAAGGGATCCTCCAGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGTGCGTG GAACTCTTGGGCTCAAGGGATCCTCCAGCCTCTGCCTCCTGAGTAGCTGGGACTACAGGTGCGTG T A AXIN1 Ensembl:ENSG00000103126 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1322084052 Functional Loss SNV dbSNP153 33..33 33 - - - 16964 RMVar_ID_16964 Human_SNP_ID_590521428 A-to-I Human chr16 - 348565 348565 348565 GAACTCTTGGGCTCAAGGGATCCTCCAGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGTGCGTG GAACTCTTGGGCTCAAGGGATCCTCCAGCCTCCGCCTCCTGAGTAGCTGGGACTACAGGTGCGTG T G AXIN1 Ensembl:ENSG00000103126 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1322084052 Functional Loss SNV dbSNP153 33..33 33 - - - 16965 RMVar_ID_16965 Human_SNP_ID_590529699 A-to-I Human chr16 - 371823 371823 371823 CCTCCTACTGAGGAGAGGGCCACCCCTCCCTCACACGCACCTCTCCTCGCCAGCTGCCTGCTCGC CCTCCTACTGAGGAGAGGGCCACCCCTCCCTCGCACGCACCTCTCCTCGCCAGCTGCCTGCTCGC T C PGAP6 Ensembl:ENSG00000129925 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1176076804 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24552055 Human_miRNA_ID_189433 16966 RMVar_ID_16966 Human_SNP_ID_590536531 A-to-I Human chr16 + 387699 387699 387699 TCGCTTGAACCCGAGAGGTGGAGGTTGCAGTGAGCCAAGATCACATCACTGCACTCCAGCCTGGG TCGCTTGAACCCGAGAGGTGGAGGTTGCAGTGGGCCAAGATCACATCACTGCACTCCAGCCTGGG A G Z97634.1 Ensembl:ENSG00000236829 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1294171763 Functional Loss SNV dbSNP153 33..33 33 - - - 16967 RMVar_ID_16967 Human_SNP_ID_590536535 A-to-I Human chr16 + 387703 387703 387703 TTGAACCCGAGAGGTGGAGGTTGCAGTGAGCCAAGATCACATCACTGCACTCCAGCCTGGGTGAC TTGAACCCGAGAGGTGGAGGTTGCAGTGAGCCGAGATCACATCACTGCACTCCAGCCTGGGTGAC A G Z97634.1 Ensembl:ENSG00000236829 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs537519120 Functional Loss SNV dbSNP153 33..33 33 - - - 16968 RMVar_ID_16968 Human_SNP_ID_590564004 A-to-I Human chr16 + 473466 473466 473466 TTTGTTTTGTTTTGTTTGAGACGGTCTGCTCTATTACTCAGGCTGGAGTGTGGTGGTACAGTCTC TTTGTTTTGTTTTGTTTGAGACGGTCTGCTCTGTTACTCAGGCTGGAGTGTGGTGGTACAGTCTC A G RAB11FIP3 Ensembl:ENSG00000090565 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1318356865 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12751005 RMVar_hsa_circ_175356,RMVar_hsa_circ_103523,RMVar_hsa_circ_294420,RMVar_hsa_circ_175355,RMVar_hsa_circ_294492,RMVar_hsa_circ_269225,RMVar_hsa_circ_122699,RMVar_hsa_circ_125620,RMVar_hsa_circ_355032,RMVar_hsa_circ_93194,RMVar_hsa_circ_175357,RMVar_hsa_circ_175358,RMVar_hsa_circ_175359 16969 RMVar_ID_16969 Human_SNP_ID_590567856 A-to-I Human chr16 + 487913 487913 487913 ACGGCGCCCCCCAGTGGTTGTGTGAGGACAGCAGCTCCCTAGGGAAGAGGCAGAGGTGCTTGAAC ACGGCGCCCCCCAGTGGTTGTGTGAGGACAGCCGCTCCCTAGGGAAGAGGCAGAGGTGCTTGAAC A C RAB11FIP3 Ensembl:ENSG00000090565 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2385130 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12753784,Human_RBP_ID_18437833 GWAS_ID_1230,GWAS_ID_1231,GWAS_ID_1232,GWAS_ID_1233,GWAS_ID_1234,GWAS_ID_1235,GWAS_ID_1236 RMVar_hsa_circ_175356,RMVar_hsa_circ_103523,RMVar_hsa_circ_294420,RMVar_hsa_circ_175355,RMVar_hsa_circ_294492,RMVar_hsa_circ_269225,RMVar_hsa_circ_122699,RMVar_hsa_circ_125620,RMVar_hsa_circ_355032,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_320314,RMVar_hsa_circ_334611,RMVar_hsa_circ_272740,RMVar_hsa_circ_175363,RMVar_hsa_circ_175364,RMVar_hsa_circ_175362 16970 RMVar_ID_16970 Human_SNP_ID_590567857 A-to-I Human chr16 + 487913 487913 487913 ACGGCGCCCCCCAGTGGTTGTGTGAGGACAGCAGCTCCCTAGGGAAGAGGCAGAGGTGCTTGAAC ACGGCGCCCCCCAGTGGTTGTGTGAGGACAGCGGCTCCCTAGGGAAGAGGCAGAGGTGCTTGAAC A G RAB11FIP3 Ensembl:ENSG00000090565 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2385130 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12753784,Human_RBP_ID_18437833 GWAS_ID_1230,GWAS_ID_1231,GWAS_ID_1232,GWAS_ID_1233,GWAS_ID_1234,GWAS_ID_1235,GWAS_ID_1236 RMVar_hsa_circ_175356,RMVar_hsa_circ_103523,RMVar_hsa_circ_294420,RMVar_hsa_circ_175355,RMVar_hsa_circ_294492,RMVar_hsa_circ_269225,RMVar_hsa_circ_122699,RMVar_hsa_circ_125620,RMVar_hsa_circ_355032,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_320314,RMVar_hsa_circ_334611,RMVar_hsa_circ_272740,RMVar_hsa_circ_175363,RMVar_hsa_circ_175364,RMVar_hsa_circ_175362 16971 RMVar_ID_16971 Human_SNP_ID_590570138 A-to-I Human chr16 + 493787 493787 493787 CATCACCACACCTGGCTAACTTTTGTATTTTTAGTAGACACGGGGTTTCACCATGTCTCAATCTC CATCACCACACCTGGCTAACTTTTGTATTTTTGGTAGACACGGGGTTTCACCATGTCTCAATCTC A G RAB11FIP3 Ensembl:ENSG00000090565 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1235355227 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12756248,Human_RBP_ID_22940105,Human_RBP_ID_23164536 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 16972 RMVar_ID_16972 Human_SNP_ID_590570154 A-to-I Human chr16 + 493814 493814 493814 TTTTTAGTAGACACGGGGTTTCACCATGTCTCAATCTCCGGACCTCGTGATCCGCCCGCCTTGAC TTTTTAGTAGACACGGGGTTTCACCATGTCTCGATCTCCGGACCTCGTGATCCGCCCGCCTTGAC A G RAB11FIP3 Ensembl:ENSG00000090565 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1274828721 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12756249 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 16973 RMVar_ID_16973 Human_SNP_ID_590570913 A-to-I Human chr16 + 496030 496030 496030 CCTCAGCCTCCCAAAGTGCTCAGATTGTAGGCATGAGCCACCACGCCCGGCCCCTCCAGTAGACT CCTCAGCCTCCCAAAGTGCTCAGATTGTAGGCGTGAGCCACCACGCCCGGCCCCTCCAGTAGACT A G RAB11FIP3 Ensembl:ENSG00000090565 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1034284853 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12756301 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 16974 RMVar_ID_16974 Human_SNP_ID_590571603 A-to-I Human chr16 + 498227 498227 498227 ACATTGTCTTGCTCTGTCACCTGGGCTGAAGTACCGTGGTGCAATCACAGCTCACTGCAGCCTGG ACATTGTCTTGCTCTGTCACCTGGGCTGAAGTCCCGTGGTGCAATCACAGCTCACTGCAGCCTGG A C RAB11FIP3 Ensembl:ENSG00000090565 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs537168412 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12756368 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_175367,RMVar_hsa_circ_104952,RMVar_hsa_circ_120827,RMVar_hsa_circ_175366 16975 RMVar_ID_16975 Human_SNP_ID_590571656 A-to-I Human chr16 + 498435 498435 498435 GGGCTGAAGGGATCCTCCCACCTTGGCCTCCCAAAGTACTGGGATCACAGGCATGAGCCGTCACA GGGCTGAAGGGATCCTCCCACCTTGGCCTCCCGAAGTACTGGGATCACAGGCATGAGCCGTCACA A G RAB11FIP3 Ensembl:ENSG00000090565 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs923841232 Functional Loss SNV dbSNP153 33..33 33 - - - 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_175367,RMVar_hsa_circ_104952,RMVar_hsa_circ_120827,RMVar_hsa_circ_175366 16976 RMVar_ID_16976 Human_SNP_ID_590571711 A-to-I Human chr16 + 498619 498619 498619 ATAGTTTTCACTTCCCAGACCTCCCAAGCTCAAATGATCCTCCCTCCTCAGCCTCCCGAGCAGCT ATAGTTTTCACTTCCCAGACCTCCCAAGCTCAGATGATCCTCCCTCCTCAGCCTCCCGAGCAGCT A G RAB11FIP3 Ensembl:ENSG00000090565 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1029062116 Functional Loss SNV dbSNP153 33..33 33 - - - 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_175367,RMVar_hsa_circ_104952,RMVar_hsa_circ_120827,RMVar_hsa_circ_175366 16977 RMVar_ID_16977 Human_SNP_ID_590571739 A-to-I Human chr16 + 498740 498740 498740 AGGCCCAGACTGGTCTTGAACTCCTGGGCTCTAGCAGTCCTCCCACCTCGGTCTCCCAGAATGTT AGGCCCAGACTGGTCTTGAACTCCTGGGCTCTTGCAGTCCTCCCACCTCGGTCTCCCAGAATGTT A T RAB11FIP3 Ensembl:ENSG00000090565 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1466838052 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12756387,Human_RBP_ID_17563907 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_175367,RMVar_hsa_circ_104952,RMVar_hsa_circ_120827,RMVar_hsa_circ_175366 16978 RMVar_ID_16978 Human_SNP_ID_590582327 A-to-I Human chr16 + 532133 532133 532133 GTGGTGGTGTGTGCCTGTAATCCCAGATACTCAGGAGGCTGAGACTGTAGAATTGCTTGAACCTG GTGGTGGTGTGTGCCTGTAATCCCAGATACTCGGGAGGCTGAGACTGTAGAATTGCTTGAACCTG A G CAPN15 Ensembl:ENSG00000103326 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1279571747 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12763832 16979 RMVar_ID_16979 Human_SNP_ID_590586066 A-to-I Human chr16 + 542641 542641 542641 ACAGGGTCTTACTCTGTCACCCAGGCTGGAGTACAGTGGTGTGATCACAGCTCACTGCAGCTTCT ACAGGGTCTTACTCTGTCACCCAGGCTGGAGTTCAGTGGTGTGATCACAGCTCACTGCAGCTTCT A T CAPN15 Ensembl:ENSG00000103326 Protein coding intron GSE47997;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,31158229,31158229 RNA-Seq:(High) rs935818276 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8726503,Human_RBP_ID_22714010,Human_RBP_ID_24414100,Human_RBP_ID_26946642 RMVar_hsa_circ_82903,RMVar_hsa_circ_125204,RMVar_hsa_circ_81438,RMVar_hsa_circ_175372,RMVar_hsa_circ_175373,RMVar_hsa_circ_175376 16980 RMVar_ID_16980 Human_SNP_ID_590605365 A-to-I Human chr16 - 587932 587932 587932 ATGTTGGTACGTGCCTGTAATCCCAGCTACTTAGGAGGCTGAGGCAGAAGAATTGCTTAAACTCG ATGTTGGTACGTGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGAAGAATTGCTTAAACTCG T C lnc-METTL26-7,lnc-METTL26-7:2,lnc-METTL26-7:3,lnc-METTL26-7:4,lnc-METTL26-7:5,lnc-METTL26-7:6 RNACentral:URS00008C32B2,RNACentral:URS0000D5CD66,RNACentral:URS0000D5DB5E,RNACentral:URS00009B0AC7,RNACentral:URS0000D5B382,RNACentral:URS0000D5BC08 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,intron,exon,exon,exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs563508386 Functional Loss SNV dbSNP153 33..33 33 - - - 16981 RMVar_ID_16981 Human_SNP_ID_590605564 A-to-I Human chr16 - 588524 588524 588524 CCACATCGACGCACCAGTTTTTTCTTTTTTGAAACAGGGTCTCCCTTTGTCGCCCAGGCTGCAGT CCACATCGACGCACCAGTTTTTTCTTTTTTGAGACAGGGTCTCCCTTTGTCGCCCAGGCTGCAGT T C lnc-METTL26-7,lnc-METTL26-7:2,lnc-METTL26-7:3,lnc-METTL26-7:4,lnc-METTL26-7:5,lnc-METTL26-7:6 RNACentral:URS00008C32B2,RNACentral:URS0000D5CD66,RNACentral:URS0000D5DB5E,RNACentral:URS00009B0AC7,RNACentral:URS0000D5B382,RNACentral:URS0000D5BC08 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,intron,intron,intron,exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs752434975 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12769354,Human_RBP_ID_18681589 16982 RMVar_ID_16982 Human_SNP_ID_590610913 A-to-I Human chr16 + 604904 604904 604904 CAACATGGTGAAACCGTATCTCTACTAAAAATACAAAGTTAGCCTGGTGTGGTGGTGGTGCTTGT CAACATGGTGAAACCGTATCTCTACTAAAAATGCAAAGTTAGCCTGGTGTGGTGGTGGTGCTTGT A G RAB40C Ensembl:ENSG00000197562 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs903756699 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_175383,RMVar_hsa_circ_119090 16983 RMVar_ID_16983 Human_SNP_ID_590616487 A-to-I Human chr16 + 622641 622641 622641 GCCATTCTCCTGCCTCAGGCTCCCGAGTAGCTAGAACTAGGTGTGCACCACCGCGTCCAGCTAAT GCCATTCTCCTGCCTCAGGCTCCCGAGTAGCTGGAACTAGGTGTGCACCACCGCGTCCAGCTAAT A G RAB40C Ensembl:ENSG00000197562 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs943261235 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25403,RMVar_hsa_circ_68144 16984 RMVar_ID_16984 Human_SNP_ID_590633868 A-to-I Human chr16 + 663174 663174 663174 AAGAAATCACATCAGTCCGGGCGTGGTGGTTCATGCCTGTGATCCCAGCACTCTGGGAGGCCAAG AAGAAATCACATCAGTCCGGGCGTGGTGGTTCGTGCCTGTGATCCCAGCACTCTGGGAGGCCAAG A G WDR90 Ensembl:ENSG00000161996 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-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 16985 RMVar_ID_16985 Human_SNP_ID_590633930 A-to-I Human chr16 + 663363 663363 663363 TGGAGGCTGAGACAAGAGAATCGCTTGAACCCAGGAGGCAGAGGTTGCAGTGAACCAAGATTGCA TGGAGGCTGAGACAAGAGAATCGCTTGAACCCTGGAGGCAGAGGTTGCAGTGAACCAAGATTGCA A T WDR90 Ensembl:ENSG00000161996 Protein coding intron GSE47997;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 23474544,29796672,31158229,31158229 RNA-Seq:(High) rs1490417529 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_175399,RMVar_hsa_circ_92716 16986 RMVar_ID_16986 Human_SNP_ID_590633933 A-to-I Human chr16 + 663387 663387 663387 TTGAACCCAGGAGGCAGAGGTTGCAGTGAACCAAGATTGCACCACTGCACTCCAGCCTGGGCGAC TTGAACCCAGGAGGCAGAGGTTGCAGTGAACCGAGATTGCACCACTGCACTCCAGCCTGGGCGAC A G WDR90 Ensembl:ENSG00000161996 Protein coding intron GSE47997;GSE99789 K562 cells&HepG2 cells;esophageal squamous carcinoma cells,EC109 - 23474544,29796672 RNA-Seq:(High) rs988630407 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22946287,Human_RBP_ID_25226489 RMVar_hsa_circ_175399,RMVar_hsa_circ_92716 16987 RMVar_ID_16987 Human_SNP_ID_590633940 A-to-I Human chr16 + 663403 663403 663403 GAGGTTGCAGTGAACCAAGATTGCACCACTGCACTCCAGCCTGGGCGACAGAGACTCCATCTCAA GAGGTTGCAGTGAACCAAGATTGCACCACTGCGCTCCAGCCTGGGCGACAGAGACTCCATCTCAA A G WDR90 Ensembl:ENSG00000161996 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1188473947 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22941728,Human_RBP_ID_25226489 RMVar_hsa_circ_175399,RMVar_hsa_circ_92716 16988 RMVar_ID_16988 Human_SNP_ID_590633941 A-to-I Human chr16 + 663403 663403 663403 GAGGTTGCAGTGAACCAAGATTGCACCACTGCACTCCAGCCTGGGCGACAGAGACTCCATCTCAA GAGGTTGCAGTGAACCAAGATTGCACCACTGCTCTCCAGCCTGGGCGACAGAGACTCCATCTCAA A T WDR90 Ensembl:ENSG00000161996 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1188473947 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22941728,Human_RBP_ID_25226489 RMVar_hsa_circ_175399,RMVar_hsa_circ_92716 16989 RMVar_ID_16989 Human_SNP_ID_590634385 A-to-I Human chr16 + 664708 664708 664708 TGAACTGAATTTTTTTTTTTTTTTTGAGACGGAGTTTCTTGTCGCCCAGGCTGGAGTGCAGTGGC TGAACTGAATTTTTTTTTTTTTTTTGAGACGGGGTTTCTTGTCGCCCAGGCTGGAGTGCAGTGGC A G WDR90 Ensembl:ENSG00000161996 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs570926654 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2481642,Human_RBP_ID_12801011 16990 RMVar_ID_16990 Human_SNP_ID_590634386 A-to-I Human chr16 + 664708 664708 664708 TGAACTGAATTTTTTTTTTTTTTTTGAGACGGAGTTTCTTGTCGCCCAGGCTGGAGTGCAGTGGC TGAACTGAATTTTTTTTTTTTTTTTGAGACGGTGTTTCTTGTCGCCCAGGCTGGAGTGCAGTGGC A T WDR90 Ensembl:ENSG00000161996 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs570926654 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2481642,Human_RBP_ID_12801011 16991 RMVar_ID_16991 Human_SNP_ID_590634440 A-to-I Human chr16 + 664878 664878 664878 ATTTTTTGTATTTTTAGTAGAGTCGGGGTTTCACCGTGTTAGCCAGGATGGTCTCGAACTCCTGA ATTTTTTGTATTTTTAGTAGAGTCGGGGTTTCCCCGTGTTAGCCAGGATGGTCTCGAACTCCTGA A C WDR90 Ensembl:ENSG00000161996 Protein coding intron GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829 esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line - 29796672,31158229 RNA-Seq:(High) rs1431905147 Functional Loss SNV dbSNP153 33..33 33 - - - 16992 RMVar_ID_16992 Human_SNP_ID_590634467 A-to-I Human chr16 + 664953 664953 664953 CGCCCACCTTGGCCTCCCAAAGGGCTGGGATTACAGGCATGAGCCACCGCGCCCGGCTGAACTGA CGCCCACCTTGGCCTCCCAAAGGGCTGGGATTGCAGGCATGAGCCACCGCGCCCGGCTGAACTGA A G WDR90 Ensembl:ENSG00000161996 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs966242989 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25226516 16993 RMVar_ID_16993 Human_SNP_ID_590649824 A-to-I Human chr16 - 698168 698168 698168 AGAAACCCCATCTCTACTAAAAATACAAAATTAGCCGGGTGTGGTGGTGGGCGCCCGAATTCCCA AGAAACCCCATCTCTACTAAAAATACAAAATTGGCCGGGTGTGGTGGTGGGCGCCCGAATTCCCA T C FBXL16 Ensembl:ENSG00000127585 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs537169054 Functional Loss SNV dbSNP153 33..33 33 - - - 16994 RMVar_ID_16994 Human_SNP_ID_590661317 A-to-I Human chr16 + 728936 728936 728936 CCTTTCCCGCCGCGGCAAGAGGGTGGGGGGGGAGGGAACAGGCTTCGGGGTGGGGGGGGCTCTCA CCTTTCCCGCCGCGGCAAGAGGGTGGGGGGGGGGGGAACAGGCTTCGGGGTGGGGGGGGCTCTCA A G HAGHL Ensembl:ENSG00000103253 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1316238865 Functional Loss SNV dbSNP153 33..33 33 - - - 16995 RMVar_ID_16995 Human_SNP_ID_590719415 A-to-I Human chr16 - 862275 862275 862275 GCTGGGCATGGTGGTGGCTGCCTATAATCCCAACTACTCGGCAGGTGGAGGTTGCAGTAAGCAGA GCTGGGCATGGTGGTGGCTGCCTATAATCCCAGCTACTCGGCAGGTGGAGGTTGCAGTAAGCAGA T C LMF1 Ensembl:ENSG00000103227 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1449921230 Functional Loss SNV dbSNP153 33..33 33 - - - 16996 RMVar_ID_16996 Human_SNP_ID_590719427 A-to-I Human chr16 - 862312 862312 862312 TGGTGAAACCCCATCTTTGCTAAAAATACAAAAATTAGCTGGGCATGGTGGTGGCTGCCTATAAT TGGTGAAACCCCATCTTTGCTAAAAATACAAAGATTAGCTGGGCATGGTGGTGGCTGCCTATAAT T C LMF1 Ensembl:ENSG00000103227 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992579490 Functional Loss SNV dbSNP153 33..33 33 - - - 16997 RMVar_ID_16997 Human_SNP_ID_590727726 A-to-I Human chr16 - 884261 884261 884261 GATTATGATGTGTAGTTTGTAGTACTATTCTAAGAGATCCGCTTCAAATACAAAGACACACAGGC GATTATGATGTGTAGTTTGTAGTACTATTCTATGAGATCCGCTTCAAATACAAAGACACACAGGC T A LMF1 Ensembl:ENSG00000103227 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1336044227 Functional Loss SNV dbSNP153 33..33 33 - - - 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_320823,RMVar_hsa_circ_60320,RMVar_hsa_circ_289792,RMVar_hsa_circ_175454,RMVar_hsa_circ_175455,RMVar_hsa_circ_175453 16998 RMVar_ID_16998 Human_SNP_ID_590728111 A-to-I Human chr16 - 885613 885613 885613 CTCCTGACTGCTGATCATATTCTCTGCTCTGAATTGTGCTTTGTCTGGTGTGACGGTGGCCAGTC CTCCTGACTGCTGATCATATTCTCTGCTCTGATTTGTGCTTTGTCTGGTGTGACGGTGGCCAGTC T A LMF1 Ensembl:ENSG00000103227 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs911613103 Functional Loss SNV dbSNP153 33..33 33 - - - 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_320823,RMVar_hsa_circ_60320,RMVar_hsa_circ_289792,RMVar_hsa_circ_175454,RMVar_hsa_circ_175455,RMVar_hsa_circ_175453 16999 RMVar_ID_16999 Human_SNP_ID_590728115 A-to-I Human chr16 - 885629 885629 885629 AACATTGTGAAATGGCCTCCTGACTGCTGATCATATTCTCTGCTCTGAATTGTGCTTTGTCTGGT AACATTGTGAAATGGCCTCCTGACTGCTGATCCTATTCTCTGCTCTGAATTGTGCTTTGTCTGGT T G LMF1 Ensembl:ENSG00000103227 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1227200745 Functional Loss SNV dbSNP153 33..33 33 - - - 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_320823,RMVar_hsa_circ_60320,RMVar_hsa_circ_289792,RMVar_hsa_circ_175454,RMVar_hsa_circ_175455,RMVar_hsa_circ_175453 17000 RMVar_ID_17000 Human_SNP_ID_590728155 A-to-I Human chr16 - 885768 885768 885768 GATAAGGGAGATTGAGATCTCCAACTATAATTATGGATTTCTCTATGTCTGCTTACATTTCTATC GATAAGGGAGATTGAGATCTCCAACTATAATTGTGGATTTCTCTATGTCTGCTTACATTTCTATC T C LMF1 Ensembl:ENSG00000103227 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1462579532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17883267 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_320823,RMVar_hsa_circ_60320,RMVar_hsa_circ_289792,RMVar_hsa_circ_175454,RMVar_hsa_circ_175455,RMVar_hsa_circ_175453 17001 RMVar_ID_17001 Human_SNP_ID_590891088 A-to-I Human chr16 - 1305793 1305793 1305793 TAATCCCAGGACTTTGGGAGGCTGAGTAGGGCAGATCGCTTGAGCTCAGGAGTTTGAGACCAGCC TAATCCCAGGACTTTGGGAGGCTGAGTAGGGCGGATCGCTTGAGCTCAGGAGTTTGAGACCAGCC T C AC120498.9 Ensembl:ENSG00000274751 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs776099905 Functional Loss SNV dbSNP153 33..33 33 - - - 17002 RMVar_ID_17002 Human_SNP_ID_590897431 A-to-I Human chr16 + 1321620 1321620 1321620 AACCCTCGTCCCTACTAAAAATACAAAAAATTAGTTGGGCGTAGTGGTGGGTGCCTCTAATCCCA AACCCTCGTCCCTACTAAAAATACAAAAAATTTGTTGGGCGTAGTGGTGGGTGCCTCTAATCCCA A T UBE2I Ensembl:ENSG00000103275 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1418455578 Functional Loss SNV dbSNP153 33..33 33 - - - 17003 RMVar_ID_17003 Human_SNP_ID_590897875 A-to-I Human chr16 + 1322686 1322686 1322686 CATGACTAGACTGGGCAACATAGCGAGACCCTATCTCTACAAAAAATTAAAAAATTTGCCAGGGG CATGACTAGACTGGGCAACATAGCGAGACCCTGTCTCTACAAAAAATTAAAAAATTTGCCAGGGG A G UBE2I Ensembl:ENSG00000103275 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs374061658 Functional Loss SNV dbSNP153 33..33 33 - - - 17004 RMVar_ID_17004 Human_SNP_ID_590897878 A-to-I Human chr16 + 1322692 1322692 1322692 TAGACTGGGCAACATAGCGAGACCCTATCTCTACAAAAAATTAAAAAATTTGCCAGGGGTGGTGG TAGACTGGGCAACATAGCGAGACCCTATCTCTCCAAAAAATTAAAAAATTTGCCAGGGGTGGTGG A C UBE2I Ensembl:ENSG00000103275 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs934952245 Functional Loss SNV dbSNP153 33..33 33 - - - 17005 RMVar_ID_17005 Human_SNP_ID_590898749 A-to-I Human chr16 + 1324523 1324523 1324523 CTTCTGCCCCCGTCAGACCACGGGACAGTCTCAGCCACGTCAGAGCCAGCATGGGCTCCCCACCA CTTCTGCCCCCGTCAGACCACGGGACAGTCTCCGCCACGTCAGAGCCAGCATGGGCTCCCCACCA A C UBE2I Ensembl:ENSG00000103275 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs761059 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12668208,Human_RBP_ID_17078468 GWAS_ID_1237,GWAS_ID_1238 17006 RMVar_ID_17006 Human_SNP_ID_590898750 A-to-I Human chr16 + 1324523 1324523 1324523 CTTCTGCCCCCGTCAGACCACGGGACAGTCTCAGCCACGTCAGAGCCAGCATGGGCTCCCCACCA CTTCTGCCCCCGTCAGACCACGGGACAGTCTCGGCCACGTCAGAGCCAGCATGGGCTCCCCACCA A G UBE2I Ensembl:ENSG00000103275 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs761059 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12668208,Human_RBP_ID_17078468 GWAS_ID_1237,GWAS_ID_1238 17007 RMVar_ID_17007 Human_SNP_ID_590900358 A-to-I Human chr16 - 1328874 1328874 1328874 TGTAGTCCCAGGCACTCGGGAGGCTGAGGCAGAAGAATCGCTTGAACCCGGGAGGTGGAGGCCGC TGTAGTCCCAGGCACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGGGAGGTGGAGGCCGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1253752662 Functional Loss SNV dbSNP153 33..33 33 - - - 17008 RMVar_ID_17008 Human_SNP_ID_590911026 A-to-I Human chr16 + 1353087 1353087 1353087 CGCCTCCCAGGTTCAAGCGATCCTCATGCCTCAGCCTCCCGAGTAGCTGGGATCACAGGCATGCA CGCCTCCCAGGTTCAAGCGATCCTCATGCCTCGGCCTCCCGAGTAGCTGGGATCACAGGCATGCA A G GNPTG Ensembl:ENSG00000090581 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1432777091 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_126151 RMVar_hsa_circ_120016,RMVar_hsa_circ_175481 17009 RMVar_ID_17009 Human_SNP_ID_590913421 A-to-I Human chr16 + 1359325 1359325 1359325 GTCTAACTCTGTAGCCCAGGCTGGAGTGCAGTAGCACGATCTTGGCTCACGGCAACCTCTCCACC GTCTAACTCTGTAGCCCAGGCTGGAGTGCAGTCGCACGATCTTGGCTCACGGCAACCTCTCCACC A C GNPTG Ensembl:ENSG00000090581 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1338247222 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27237041 RMVar_hsa_circ_120016,RMVar_hsa_circ_175481 17010 RMVar_ID_17010 Human_SNP_ID_590913439 A-to-I Human chr16 + 1359368 1359368 1359368 GGCTCACGGCAACCTCTCCACCTCCCAGGCTCAAGGAATTCTCCTGCCTCAGCCTCCCGAGTAGC GGCTCACGGCAACCTCTCCACCTCCCAGGCTCGAGGAATTCTCCTGCCTCAGCCTCCCGAGTAGC A G GNPTG Ensembl:ENSG00000090581 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1291627251 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120016,RMVar_hsa_circ_175481 17011 RMVar_ID_17011 Human_SNP_ID_590913454 A-to-I Human chr16 + 1359398 1359398 1359398 TCAAGGAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTGCAGGCATCCGCCATCACGCCTG TCAAGGAATTCTCCTGCCTCAGCCTCCCGAGTGGCTGGGACTGCAGGCATCCGCCATCACGCCTG A G GNPTG Ensembl:ENSG00000090581 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs570183840 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120016,RMVar_hsa_circ_175481 17012 RMVar_ID_17012 Human_SNP_ID_590913613 A-to-I Human chr16 + 1359860 1359860 1359860 GGCTGGGCGCTGGGGCTCACGCCTGTAATCCCAGTACTTTAGGAGGCTGAGGCAGGTGGATCACC GGCTGGGCGCTGGGGCTCACGCCTGTAATCCCGGTACTTTAGGAGGCTGAGGCAGGTGGATCACC A G GNPTG Ensembl:ENSG00000090581 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1223217254 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120016,RMVar_hsa_circ_175481 17013 RMVar_ID_17013 Human_SNP_ID_590913617 A-to-I Human chr16 + 1359868 1359868 1359868 GCTGGGGCTCACGCCTGTAATCCCAGTACTTTAGGAGGCTGAGGCAGGTGGATCACCTGAGGTCA GCTGGGGCTCACGCCTGTAATCCCAGTACTTTGGGAGGCTGAGGCAGGTGGATCACCTGAGGTCA A G GNPTG Ensembl:ENSG00000090581 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1277074446 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120016,RMVar_hsa_circ_175481 17014 RMVar_ID_17014 Human_SNP_ID_590913645 A-to-I Human chr16 + 1359962 1359962 1359962 AGAAACCCCGTCTCTACAAAAATACAAAAATTAGCCAGCCGTGATGGCAGGCACCGGTAATCCTA AGAAACCCCGTCTCTACAAAAATACAAAAATTGGCCAGCCGTGATGGCAGGCACCGGTAATCCTA A G GNPTG Ensembl:ENSG00000090581 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs113347247 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120016,RMVar_hsa_circ_175481 17015 RMVar_ID_17015 Human_SNP_ID_590913656 A-to-I Human chr16 + 1359998 1359998 1359998 AGCCGTGATGGCAGGCACCGGTAATCCTAGCTACTGGGGAGACTGAGGCGGGAAAATCGGTTGAA AGCCGTGATGGCAGGCACCGGTAATCCTAGCTCCTGGGGAGACTGAGGCGGGAAAATCGGTTGAA A C GNPTG Ensembl:ENSG00000090581 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs989963886 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120016,RMVar_hsa_circ_175481 17016 RMVar_ID_17016 Human_SNP_ID_590913684 A-to-I Human chr16 + 1360068 1360068 1360068 TGGTGGAGATTGTAGTGAGCCAAGATCGTGCCACTGCAATCCAGCCTGGCGACAATGCTAGACTC TGGTGGAGATTGTAGTGAGCCAAGATCGTGCCGCTGCAATCCAGCCTGGCGACAATGCTAGACTC A G GNPTG Ensembl:ENSG00000090581 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs954021765 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9060178 RMVar_hsa_circ_120016,RMVar_hsa_circ_175481 17017 RMVar_ID_17017 Human_SNP_ID_590913806 A-to-I Human chr16 + 1360363 1360363 1360363 GTTAGTCTTTCAGGCCGGGCATAGTGGCTCACACCTGTAATCCCAGCACTTGGGAGGCCAAGGTG GTTAGTCTTTCAGGCCGGGCATAGTGGCTCACGCCTGTAATCCCAGCACTTGGGAGGCCAAGGTG A G GNPTG Ensembl:ENSG00000090581 Protein coding intron GSE100210;GSE99789 HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 29129909,29796672 RNA-Seq:(High) rs1266222254 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120016,RMVar_hsa_circ_175481 17018 RMVar_ID_17018 Human_SNP_ID_590913813 A-to-I Human chr16 + 1360390 1360390 1360390 CTCACACCTGTAATCCCAGCACTTGGGAGGCCAAGGTGGACGGATCACTTCAGGTCCACAGTTGC CTCACACCTGTAATCCCAGCACTTGGGAGGCCGAGGTGGACGGATCACTTCAGGTCCACAGTTGC A G GNPTG Ensembl:ENSG00000090581 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1352799260 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120016,RMVar_hsa_circ_175481 17019 RMVar_ID_17019 Human_SNP_ID_590914022 A-to-I Human chr16 + 1360956 1360956 1360956 GAATGTCCTCTTTTTTGGGGGGTGGGGAAGACAGGGTCTTGCTCTGTCACGCAGGCTGGAGTGCA GAATGTCCTCTTTTTTGGGGGGTGGGGAAGACGGGGTCTTGCTCTGTCACGCAGGCTGGAGTGCA A G GNPTG Ensembl:ENSG00000090581 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1395761154 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_233225 RMVar_hsa_circ_120016,RMVar_hsa_circ_175481 17020 RMVar_ID_17020 Human_SNP_ID_590914044 A-to-I Human chr16 + 1361002 1361002 1361002 TCACGCAGGCTGGAGTGCAGTGGTACGATCTCAGCTCACTGCACTCTCCACCTCCTGGGTTCAAG TCACGCAGGCTGGAGTGCAGTGGTACGATCTCGGCTCACTGCACTCTCCACCTCCTGGGTTCAAG A G GNPTG Ensembl:ENSG00000090581 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs951059459 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120016,RMVar_hsa_circ_175481 17021 RMVar_ID_17021 Human_SNP_ID_590914045 A-to-I Human chr16 + 1361002 1361002 1361002 TCACGCAGGCTGGAGTGCAGTGGTACGATCTCAGCTCACTGCACTCTCCACCTCCTGGGTTCAAG TCACGCAGGCTGGAGTGCAGTGGTACGATCTCTGCTCACTGCACTCTCCACCTCCTGGGTTCAAG A T GNPTG Ensembl:ENSG00000090581 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs951059459 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120016,RMVar_hsa_circ_175481 17022 RMVar_ID_17022 Human_SNP_ID_590914096 A-to-I Human chr16 + 1361179 1361177 1361179 CCCAGGCTGGTGTCATACTCCTGGCCTCAAGCAATCTTCCCGCCTTGGCCTCCCAAAGTGCTGGG CCCAGGCTGGTGTCATACTCCTGGCCTCAAG__ATCTTCCCGCCTTGGCCTCCCAAAGTGCTGGG GCA G GNPTG Ensembl:ENSG00000090581 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1427926658 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_120016,RMVar_hsa_circ_175481 17023 RMVar_ID_17023 Human_SNP_ID_590914098 A-to-I Human chr16 + 1361179 1361179 1361179 CCCAGGCTGGTGTCATACTCCTGGCCTCAAGCAATCTTCCCGCCTTGGCCTCCCAAAGTGCTGGG CCCAGGCTGGTGTCATACTCCTGGCCTCAAGCCATCTTCCCGCCTTGGCCTCCCAAAGTGCTGGG A C GNPTG Ensembl:ENSG00000090581 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs981153792 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120016,RMVar_hsa_circ_175481 17024 RMVar_ID_17024 Human_SNP_ID_590914167 A-to-I Human chr16 + 1361382 1361382 1361382 AAAACTGGTCCTTGGCCGGGCGCGGTGGCTCAAACCTGTAATCCCAGCACTTTGGGAGGCCGAGG AAAACTGGTCCTTGGCCGGGCGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGG A C GNPTG Ensembl:ENSG00000090581 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs565187240 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_126152 RMVar_hsa_circ_120016,RMVar_hsa_circ_175481 17025 RMVar_ID_17025 Human_SNP_ID_590914277 A-to-I Human chr16 + 1361593 1361593 1361593 GTGAACATGGGAGGCGGAGCTTGAAGTGAGCCAAGATCATGCCACTGCACTCCAGCCTGGGTGAC GTGAACATGGGAGGCGGAGCTTGAAGTGAGCCGAGATCATGCCACTGCACTCCAGCCTGGGTGAC A G GNPTG Ensembl:ENSG00000090581 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs565070200 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120016,RMVar_hsa_circ_175481 17026 RMVar_ID_17026 Human_SNP_ID_590915420 A-to-I Human chr16 + 1363268 1363268 1363268 TGATAAAAATAACTCCATGAATTCTGTAAACCATTGCATAAATGCTATAGTGTAAAAAAATTTAA TGATAAAAATAACTCCATGAATTCTGTAAACCGTTGCATAAATGCTATAGTGTAAAAAAATTTAA A G GNPTG Ensembl:ENSG00000090581 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs949569930 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_468485,Human_RBP_ID_1512567,Human_RBP_ID_1838197,Human_RBP_ID_3491402,Human_RBP_ID_17653202 17027 RMVar_ID_17027 Human_SNP_ID_590915752 A-to-I Human chr16 + 1364092 1364092 1364092 TCCAAATGGGAACCAAGTGCATAAATACAAATAAAAACAGAGTTTACACATCGATGACAGTAGCA TCCAAATGGGAACCAAGTGCATAAATACAAATGAAAACAGAGTTTACACATCGATGACAGTAGCA A G GNPTG Ensembl:ENSG00000090581 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs185646663 Functional Loss SNV dbSNP153 33..33 33 - - - 17028 RMVar_ID_17028 Human_SNP_ID_590916193 A-to-I Human chr16 - 1365070 1365070 1365070 AGAATCGCTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCCGAGATCGCGCCACCGCACTCCAGCC AGAATCGCTTGAACCTGGGAGGCAGAGGTTGCTGTGAGCCGAGATCGCGCCACCGCACTCCAGCC T A UNKL Ensembl:ENSG00000059145 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1267482387 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25191533 Human_miRNA_ID_619407 17029 RMVar_ID_17029 Human_SNP_ID_590918127 A-to-I Human chr16 - 1368684 1368684 1368684 GTTGGCCATACTGGTCTCAAACTCCTGACCTCAAGTGATCTGCTGGCCTCGACCTCCCAAAGTGC GTTGGCCATACTGGTCTCAAACTCCTGACCTCGAGTGATCTGCTGGCCTCGACCTCCCAAAGTGC T C UNKL Ensembl:ENSG00000059145 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs894120863 Functional Loss SNV dbSNP153 33..33 33 - - - 17030 RMVar_ID_17030 Human_SNP_ID_590918131 A-to-I Human chr16 - 1368698 1368698 1368698 TGGAGTTTCACCATGTTGGCCATACTGGTCTCAAACTCCTGACCTCAAGTGATCTGCTGGCCTCG TGGAGTTTCACCATGTTGGCCATACTGGTCTCCAACTCCTGACCTCAAGTGATCTGCTGGCCTCG T G UNKL Ensembl:ENSG00000059145 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1378450654 Functional Loss SNV dbSNP153 33..33 33 - - - 17031 RMVar_ID_17031 Human_SNP_ID_590918141 A-to-I Human chr16 - 1368744 1368744 1368744 GGTACCTGCTACCACGCCAGGCTAATTTTTGTATTTTTAGTAGAGATGGAGTTTCACCATGTTGG GGTACCTGCTACCACGCCAGGCTAATTTTTGTGTTTTTAGTAGAGATGGAGTTTCACCATGTTGG T C UNKL Ensembl:ENSG00000059145 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1343616214 Functional Loss SNV dbSNP153 33..33 33 - - - 17032 RMVar_ID_17032 Human_SNP_ID_590918227 A-to-I Human chr16 - 1369019 1369019 1369019 TACTTTGGGCCAACATAGTGGCTCAAGCCTGTAATCCCAGCACTTTGGGAGGTCGAGGTGGGTGG TACTTTGGGCCAACATAGTGGCTCAAGCCTGTGATCCCAGCACTTTGGGAGGTCGAGGTGGGTGG T C UNKL Ensembl:ENSG00000059145 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1014816794 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17563676 17033 RMVar_ID_17033 Human_SNP_ID_590918367 A-to-I Human chr16 - 1369237 1369236 1369237 GGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGGCGGGCGTGGTGGCACATGCCTGTAATC GGTGAAACCCCGTCTCTACTAAAAATACAAAA_TTAGGCGGGCGTGGTGGCACATGCCTGTAATC AT A UNKL Ensembl:ENSG00000059145 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1479104460 Functional Loss DEL dbSNP153 33..33 33 - - - 17034 RMVar_ID_17034 Human_SNP_ID_590918581 A-to-I Human chr16 - 1369831 1369831 1369831 AGCTGGGACTACAGGCGGGCGCCACCACGCCCAGCTAGTTTTTGTATTTTTAGTAGAGATGGCGT AGCTGGGACTACAGGCGGGCGCCACCACGCCCCGCTAGTTTTTGTATTTTTAGTAGAGATGGCGT T G UNKL Ensembl:ENSG00000059145 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1442124309 Functional Loss SNV dbSNP153 33..33 33 - - - 17035 RMVar_ID_17035 Human_SNP_ID_590956894 A-to-I Human chr16 - 1473664 1473664 1473664 TTGTGCTTAAAGATTAGGAAGGACGGCAGGGCACGGTGGCTCACATCTGTAATCCCAGCACTTTG TTGTGCTTAAAGATTAGGAAGGACGGCAGGGCGCGGTGGCTCACATCTGTAATCCCAGCACTTTG T C CLCN7 Ensembl:ENSG00000103249 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs933213506 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12672812 17036 RMVar_ID_17036 Human_SNP_ID_590957000 A-to-I Human chr16 - 1473972 1473972 1473972 TTAAGTGACTCTCCTGCCTCAGCCTCCTGAGTAGCTGGAATTACAGGCGTGCGCCACCGCGCCCG TTAAGTGACTCTCCTGCCTCAGCCTCCTGAGTGGCTGGAATTACAGGCGTGCGCCACCGCGCCCG T C CLCN7 Ensembl:ENSG00000103249 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1030119408 Functional Loss SNV dbSNP153 33..33 33 - - - 17037 RMVar_ID_17037 Human_SNP_ID_590970095 A-to-I Human chr16 + 1509828 1509828 1509828 TGCCTCAGCTTTGCTTGTCACTCTCGTCTGGCAGACGTGGCTGAGAAAGACCCGGACGAGGACTG TGCCTCAGCTTTGCTTGTCACTCTCGTCTGGCGGACGTGGCTGAGAAAGACCCGGACGAGGACTG A G TELO2 Ensembl:ENSG00000100726 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1217033632 Functional Loss SNV dbSNP153 33..33 33 - - - 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 17038 RMVar_ID_17038 Human_SNP_ID_591009481 A-to-I Human chr16 + 1635072 1635072 1635072 AGGTGTGCACCACCACACCCAGCTAATTTTATATTTTTTAGGAGAGATGAGGTTTCACTATGTTG AGGTGTGCACCACCACACCCAGCTAATTTTATGTTTTTTAGGAGAGATGAGGTTTCACTATGTTG A G AL031708.1,CRAMP1 Ensembl:ENSG00000261732,Ensembl:ENSG00000007545 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs901017747 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_360965,RMVar_hsa_circ_175524,RMVar_hsa_circ_277027,RMVar_hsa_circ_374387,RMVar_hsa_circ_281754,RMVar_hsa_circ_80539,RMVar_hsa_circ_175525,RMVar_hsa_circ_175522,RMVar_hsa_circ_175523,RMVar_hsa_circ_340916,RMVar_hsa_circ_277697,RMVar_hsa_circ_175527,RMVar_hsa_circ_112301,RMVar_hsa_circ_175526 17039 RMVar_ID_17039 Human_SNP_ID_591009507 A-to-I Human chr16 + 1635172 1635172 1635172 CACCTGCCTCGGCCTCCCAAAGTGCAAGGATTACAGGCGTGAGCCACCACGCCTGGCCTGTGCTT CACCTGCCTCGGCCTCCCAAAGTGCAAGGATTCCAGGCGTGAGCCACCACGCCTGGCCTGTGCTT A C AL031708.1,CRAMP1 Ensembl:ENSG00000261732,Ensembl:ENSG00000007545 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1161728292 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_360965,RMVar_hsa_circ_175524,RMVar_hsa_circ_277027,RMVar_hsa_circ_374387,RMVar_hsa_circ_281754,RMVar_hsa_circ_80539,RMVar_hsa_circ_175525,RMVar_hsa_circ_175522,RMVar_hsa_circ_175523,RMVar_hsa_circ_340916,RMVar_hsa_circ_277697,RMVar_hsa_circ_175527,RMVar_hsa_circ_112301,RMVar_hsa_circ_175526 17040 RMVar_ID_17040 Human_SNP_ID_591024463 A-to-I Human chr16 + 1682516 1682516 1682516 CAACATGGTGAAACCCCGTCTCTACTAAAAATAGAAAAATTAGCTGGGCATGGTGGCGGGCATCT CAACATGGTGAAACCCCGTCTCTACTAAAAATTGAAAAATTAGCTGGGCATGGTGGCGGGCATCT A T AL031708.1,JPT2 Ensembl:ENSG00000261732,Ensembl:ENSG00000206053 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs914772582 Functional Loss SNV dbSNP153 33..33 33 - - - 17041 RMVar_ID_17041 Human_SNP_ID_591025872 A-to-I Human chr16 + 1687122 1687122 1687122 CTTTTTCCTCAGCCTCCTGAGTGGCTGGGACTACGGGCGTATGCCACCATGCTTAGGTAATTTTT CTTTTTCCTCAGCCTCCTGAGTGGCTGGGACTGCGGGCGTATGCCACCATGCTTAGGTAATTTTT A G JPT2 Ensembl:ENSG00000206053 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1252627350 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17872293 RMVar_hsa_circ_295159,RMVar_hsa_circ_356801,RMVar_hsa_circ_357002,RMVar_hsa_circ_283954 17042 RMVar_ID_17042 Human_SNP_ID_591025892 A-to-I Human chr16 + 1687187 1687187 1687187 TTTTGTATTTTTTGTGGAGACAGGGTTTAACCATGTTGCCTAGGCTGGTCTCGAACTCCTGGGCT TTTTGTATTTTTTGTGGAGACAGGGTTTAACCTTGTTGCCTAGGCTGGTCTCGAACTCCTGGGCT A T JPT2 Ensembl:ENSG00000206053 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs777149694 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_295159,RMVar_hsa_circ_356801,RMVar_hsa_circ_357002,RMVar_hsa_circ_283954 17043 RMVar_ID_17043 Human_SNP_ID_591047303 A-to-I Human chr16 + 1753916 1753916 1753916 CTAGGACCGGCCGGGCACAGTGGCTCACGCCTATAATCCCAGCACTCTGGGAGGCCGAGGCGGGT CTAGGACCGGCCGGGCACAGTGGCTCACGCCTGTAATCCCAGCACTCTGGGAGGCCGAGGCGGGT A G MAPK8IP3 Ensembl:ENSG00000138834 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1267197372 Functional Loss SNV dbSNP153 33..33 33 - - - 17044 RMVar_ID_17044 Human_SNP_ID_591047449 A-to-I Human chr16 + 1754502 1754502 1754502 ATGTAGAAACTGTCCACAAATAGGCCGGGCACAGTGGTTCATGCCTGTCATCCCAGCACTGTGGG ATGTAGAAACTGTCCACAAATAGGCCGGGCACTGTGGTTCATGCCTGTCATCCCAGCACTGTGGG A T MAPK8IP3 Ensembl:ENSG00000138834 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1346788014 Functional Loss SNV dbSNP153 33..33 33 - - - 17045 RMVar_ID_17045 Human_SNP_ID_591048072 A-to-I Human chr16 + 1756715 1756715 1756715 GTGGTGGCATGTACCTGTAGACTCAGCTACTCAGGAGGCTGAGGTGGGAGGATCTCTTGAGCCTG GTGGTGGCATGTACCTGTAGACTCAGCTACTCTGGAGGCTGAGGTGGGAGGATCTCTTGAGCCTG A T MAPK8IP3 Ensembl:ENSG00000138834 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs998844371 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_128560 17046 RMVar_ID_17046 Human_SNP_ID_591052852 A-to-I Human chr16 + 1768603 1768603 1768603 GCTGCGGAACGTGCTGGTGCTGAGCGGCGGGGAGGGCTACATCGACTTCCGCATTGGTGAGCGGG GCTGCGGAACGTGCTGGTGCTGAGCGGCGGGGGGGGCTACATCGACTTCCGCATTGGTGAGCGGG A G MAPK8IP3 Ensembl:ENSG00000138834 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs770197203 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_891161,Human_RBP_ID_5523884,Human_RBP_ID_18163459,Human_RBP_ID_18469626,Human_RBP_ID_18982956 Human_Splice_Rec_1660151,Human_Splice_Rec_1660211,Human_Splice_Rec_1660269,Human_Splice_Rec_1660329,Human_Splice_Rec_1660411 17047 RMVar_ID_17047 Human_SNP_ID_591054463 A-to-I Human chr16 - 1771412 1771412 1771412 CCGGCCTGACGGCCCGTCCCCGCCTGCCCCGCAGCCTGCACCGGCGCACACGAACGCACCTTCCT CCGGCCTGACGGCCCGTCCCCGCCTGCCCCGCGGCCTGCACCGGCGCACACGAACGCACCTTCCT T C NME3 Ensembl:ENSG00000103024 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1470560602 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5182106,Human_RBP_ID_22356660 17048 RMVar_ID_17048 Human_SNP_ID_591060772 A-to-I Human chr16 + 1784123 1784123 1784123 GAAGCTTTTTTTTTTTTTTGAGACAGGGTCTTAACTGTCGCCAAGGCTGAAGTGCAGTGGCACGA GAAGCTTTTTTTTTTTTTTGAGACAGGGTCTTTACTGTCGCCAAGGCTGAAGTGCAGTGGCACGA A T NUBP2 Ensembl:ENSG00000095906 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1034719189 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5419009 17049 RMVar_ID_17049 Human_SNP_ID_591060997 A-to-I Human chr16 + 1784815 1784815 1784815 TAATCCCAGCACTTTGGGAGGCCGAGGCGGGCAGATCACTTGAGGTCAGATTTGAGACCAGCATG TAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGGATCACTTGAGGTCAGATTTGAGACCAGCATG A G NUBP2 Ensembl:ENSG00000095906 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041398263 Functional Loss SNV dbSNP153 33..33 33 - - - 17050 RMVar_ID_17050 Human_SNP_ID_591061026 A-to-I Human chr16 + 1784898 1784898 1784898 TCTCTACGAAAAAAATAAAAAATTAGCTGGGCATGGTGGCGCACGCCTGTGGTCCCAGGTACTCT TCTCTACGAAAAAAATAAAAAATTAGCTGGGCTTGGTGGCGCACGCCTGTGGTCCCAGGTACTCT A T NUBP2 Ensembl:ENSG00000095906 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1007763537 Functional Loss SNV dbSNP153 33..33 33 - - - 17051 RMVar_ID_17051 Human_SNP_ID_591061048 A-to-I Human chr16 + 1784963 1784963 1784963 GGAAGCTGAGGCGTGGGAGGCTGAGGCACGAGAATTGCTTGGACCCAGGAGGCGGAGGTTGCAGT GGAAGCTGAGGCGTGGGAGGCTGAGGCACGAGGATTGCTTGGACCCAGGAGGCGGAGGTTGCAGT A G NUBP2 Ensembl:ENSG00000095906 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1476963025 Functional Loss SNV dbSNP153 33..33 33 - - - 17052 RMVar_ID_17052 Human_SNP_ID_591121785 A-to-I Human chr16 - 1962177 1962175 1962178 GGAGACTGTATTCACCAAGTCTCCCTATCAGGAGTTCACTGACCACCTCGTCAAGACCCACACCA GGAGACTGTATTCACCAAGTCTCCCTATCAG___TTCACTGACCACCTCGTCAAGACCCACACCA ACTC A RPS2 Ensembl:ENSG00000140988 Protein coding CDS GSE56152 embryonic stem cells,wild type - 25708366 RNA-Seq:(High) 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 17053 RMVar_ID_17053 Human_SNP_ID_591142899 A-to-I Human chr16 + 2013839 2013839 2013839 CAGAAATTAGCTGAGCGTTTTGGCAGGCACCTATAATCCCAGCTACTTGGGAGGCTGAGTCAGGA CAGAAATTAGCTGAGCGTTTTGGCAGGCACCTGTAATCCCAGCTACTTGGGAGGCTGAGTCAGGA A G NPW Ensembl:ENSG00000183971 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1253581599 Functional Loss SNV dbSNP153 33..33 33 - - - 17054 RMVar_ID_17054 Human_SNP_ID_591148751 A-to-I Human chr16 + 2030794 2030794 2030794 AAACCCCCGTCTCTACTAAAAATACAAAAATCAGTTGGGCATGGTGGGGCACGCCTATAGTCCCA AAACCCCCGTCTCTACTAAAAATACAAAAATCCGTTGGGCATGGTGGGGCACGCCTATAGTCCCA A C SLC9A3R2 Ensembl:ENSG00000065054 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1304875753 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_378712 17055 RMVar_ID_17055 Human_SNP_ID_591148752 A-to-I Human chr16 + 2030794 2030794 2030794 AAACCCCCGTCTCTACTAAAAATACAAAAATCAGTTGGGCATGGTGGGGCACGCCTATAGTCCCA AAACCCCCGTCTCTACTAAAAATACAAAAATCTGTTGGGCATGGTGGGGCACGCCTATAGTCCCA A T SLC9A3R2 Ensembl:ENSG00000065054 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1304875753 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_378712 17056 RMVar_ID_17056 Human_SNP_ID_591148759 A-to-I Human chr16 + 2030812 2030812 2030812 AAAATACAAAAATCAGTTGGGCATGGTGGGGCACGCCTATAGTCCCAGCTACTTGGGAGGCTGAG AAAATACAAAAATCAGTTGGGCATGGTGGGGCTCGCCTATAGTCCCAGCTACTTGGGAGGCTGAG A T SLC9A3R2 Ensembl:ENSG00000065054 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs907083433 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_378712 17057 RMVar_ID_17057 Human_SNP_ID_591148764 A-to-I Human chr16 + 2030818 2030818 2030818 CAAAAATCAGTTGGGCATGGTGGGGCACGCCTATAGTCCCAGCTACTTGGGAGGCTGAGGCAGGA CAAAAATCAGTTGGGCATGGTGGGGCACGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGA A G SLC9A3R2 Ensembl:ENSG00000065054 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1002566880 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_378712 17058 RMVar_ID_17058 Human_SNP_ID_591148788 A-to-I Human chr16 + 2030916 2030916 2030916 TGAGCCGAGATCCCGCCATAGCACTCCAGCCTAGGCGACAGAGTGAGACTGTCTCAAAAAAAAAC TGAGCCGAGATCCCGCCATAGCACTCCAGCCTGGGCGACAGAGTGAGACTGTCTCAAAAAAAAAC A G SLC9A3R2 Ensembl:ENSG00000065054 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285913809 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_378712 17059 RMVar_ID_17059 Human_SNP_ID_591151606 A-to-I Human chr16 - 2038034 2038034 2038034 AGGCTGGGGGAGCTCGGGGCAGGCTGAGGCCCAAGGTCCGTGCGGGAGGGGTCCCAGGGTCCCGA AGGCTGGGGGAGCTCGGGGCAGGCTGAGGCCCGAGGTCCGTGCGGGAGGGGTCCCAGGGTCCCGA T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs750261031 Functional Loss SNV dbSNP153 33..33 33 - - - 17060 RMVar_ID_17060 Human_SNP_ID_591151607 A-to-I Human chr16 - 2038034 2038034 2038034 AGGCTGGGGGAGCTCGGGGCAGGCTGAGGCCCAAGGTCCGTGCGGGAGGGGTCCCAGGGTCCCGA AGGCTGGGGGAGCTCGGGGCAGGCTGAGGCCCCAGGTCCGTGCGGGAGGGGTCCCAGGGTCCCGA T G - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs750261031 Functional Loss SNV dbSNP153 33..33 33 - - - 17061 RMVar_ID_17061 Human_SNP_ID_591156883 A-to-I Human chr16 + 2052507 2052507 2052507 AAGTTTTGTATTTTTTGTCGTGACAGGGTCTCACTGTGTTGCCCAGGCTAGTCTGAAACTCCTGG AAGTTTTGTATTTTTTGTCGTGACAGGGTCTCGCTGTGTTGCCCAGGCTAGTCTGAAACTCCTGG A G TSC2 Ensembl:ENSG00000103197 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs528047409 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44427,RMVar_hsa_circ_175617,RMVar_hsa_circ_79940,RMVar_hsa_circ_175618 17062 RMVar_ID_17062 Human_SNP_ID_591156890 A-to-I Human chr16 + 2052524 2052524 2052524 TCGTGACAGGGTCTCACTGTGTTGCCCAGGCTAGTCTGAAACTCCTGGGCTGACGTGACCCTCTC TCGTGACAGGGTCTCACTGTGTTGCCCAGGCTGGTCTGAAACTCCTGGGCTGACGTGACCCTCTC A G TSC2 Ensembl:ENSG00000103197 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs776483319 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44427,RMVar_hsa_circ_175617,RMVar_hsa_circ_79940,RMVar_hsa_circ_175618 17063 RMVar_ID_17063 Human_SNP_ID_591163077 A-to-I Human chr16 + 2067258 2067258 2067258 ATAGCTCAGTGCAGCCTTGAACTCCTGTGACCAAGTGATCGTCCTGCCTCGGAGGCCTCCCAAGT ATAGCTCAGTGCAGCCTTGAACTCCTGTGACCCAGTGATCGTCCTGCCTCGGAGGCCTCCCAAGT A C TSC2 Ensembl:ENSG00000103197 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1464028570 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12684477 RMVar_hsa_circ_175617,RMVar_hsa_circ_79940,RMVar_hsa_circ_127127,RMVar_hsa_circ_175624,RMVar_hsa_circ_83918,RMVar_hsa_circ_93925,RMVar_hsa_circ_175625,RMVar_hsa_circ_98962,RMVar_hsa_circ_175623,RMVar_hsa_circ_82864,RMVar_hsa_circ_9364,RMVar_hsa_circ_81580,RMVar_hsa_circ_175627,RMVar_hsa_circ_175626,RMVar_hsa_circ_118077,RMVar_hsa_circ_103700,RMVar_hsa_circ_175629,RMVar_hsa_circ_175630,RMVar_hsa_circ_110039,RMVar_hsa_circ_370428,RMVar_hsa_circ_87409,RMVar_hsa_circ_99668,RMVar_hsa_circ_175632,RMVar_hsa_circ_175633,RMVar_hsa_circ_175634,RMVar_hsa_circ_175631,RMVar_hsa_circ_76248,RMVar_hsa_circ_175635,RMVar_hsa_circ_175636,RMVar_hsa_circ_34709,RMVar_hsa_circ_321473,RMVar_hsa_circ_371431,RMVar_hsa_circ_94051,RMVar_hsa_circ_175637,RMVar_hsa_circ_175638 17064 RMVar_ID_17064 Human_SNP_ID_591163093 A-to-I Human chr16 + 2067291 2067291 2067291 AGTGATCGTCCTGCCTCGGAGGCCTCCCAAGTAGCTGGGACCATAGGCACACGTCACCACACCTG AGTGATCGTCCTGCCTCGGAGGCCTCCCAAGTCGCTGGGACCATAGGCACACGTCACCACACCTG A C TSC2 Ensembl:ENSG00000103197 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1432816451 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12684477 RMVar_hsa_circ_175617,RMVar_hsa_circ_79940,RMVar_hsa_circ_127127,RMVar_hsa_circ_175624,RMVar_hsa_circ_83918,RMVar_hsa_circ_93925,RMVar_hsa_circ_175625,RMVar_hsa_circ_98962,RMVar_hsa_circ_175623,RMVar_hsa_circ_82864,RMVar_hsa_circ_9364,RMVar_hsa_circ_81580,RMVar_hsa_circ_175627,RMVar_hsa_circ_175626,RMVar_hsa_circ_118077,RMVar_hsa_circ_103700,RMVar_hsa_circ_175629,RMVar_hsa_circ_175630,RMVar_hsa_circ_110039,RMVar_hsa_circ_370428,RMVar_hsa_circ_87409,RMVar_hsa_circ_99668,RMVar_hsa_circ_175632,RMVar_hsa_circ_175633,RMVar_hsa_circ_175634,RMVar_hsa_circ_175631,RMVar_hsa_circ_76248,RMVar_hsa_circ_175635,RMVar_hsa_circ_175636,RMVar_hsa_circ_34709,RMVar_hsa_circ_321473,RMVar_hsa_circ_371431,RMVar_hsa_circ_94051,RMVar_hsa_circ_175637,RMVar_hsa_circ_175638 17065 RMVar_ID_17065 Human_SNP_ID_591169724 A-to-I Human chr16 - 2080665 2080665 2080665 CCTGGCTAACACAGTGAAACCCCATCTCTACTAGAAATACAAAAAAATTGGCCAGGCGTGGTGGC CCTGGCTAACACAGTGAAACCCCATCTCTACTGGAAATACAAAAAAATTGGCCAGGCGTGGTGGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1434987625 Functional Loss SNV dbSNP153 33..33 33 - - - 17066 RMVar_ID_17066 Human_SNP_ID_591169734 A-to-I Human chr16 - 2080674 2080674 2080674 TGAGACCATCCTGGCTAACACAGTGAAACCCCATCTCTACTAGAAATACAAAAAAATTGGCCAGG TGAGACCATCCTGGCTAACACAGTGAAACCCCGTCTCTACTAGAAATACAAAAAAATTGGCCAGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs368981283 Functional Loss SNV dbSNP153 33..33 33 - - - 17067 RMVar_ID_17067 Human_SNP_ID_591169735 A-to-I Human chr16 - 2080674 2080674 2080674 TGAGACCATCCTGGCTAACACAGTGAAACCCCATCTCTACTAGAAATACAAAAAAATTGGCCAGG TGAGACCATCCTGGCTAACACAGTGAAACCCCCTCTCTACTAGAAATACAAAAAAATTGGCCAGG T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs368981283 Functional Loss SNV dbSNP153 33..33 33 - - - 17068 RMVar_ID_17068 Human_SNP_ID_591185029 A-to-I Human chr16 - 2105937 2105937 2105937 TGGCTGCACGGGCTCACCGCTAGTGTGCTCCCAGGGCTGCTGCGGCAGGCCGATCCCCAGCACGT TGGCTGCACGGGCTCACCGCTAGTGTGCTCCCGGGGCTGCTGCGGCAGGCCGATCCCCAGCACGT T C PKD1 Ensembl:ENSG00000008710 Protein coding CDS GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) 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 17069 RMVar_ID_17069 Human_SNP_ID_591197257 A-to-I Human chr16 - 2131740 2131740 2131740 CGGCTCACTGCAGCCTCCATCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCT CGGCTCACTGCAGCCTCCATCTCCCGGGTTCAGGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCT T C PKD1 Ensembl:ENSG00000008710 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1453751893 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91519,RMVar_hsa_circ_175688,RMVar_hsa_circ_96554,RMVar_hsa_circ_175691 17070 RMVar_ID_17070 Human_SNP_ID_591197258 A-to-I Human chr16 - 2131740 2131740 2131740 CGGCTCACTGCAGCCTCCATCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCT CGGCTCACTGCAGCCTCCATCTCCCGGGTTCACGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCT T G PKD1 Ensembl:ENSG00000008710 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1453751893 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91519,RMVar_hsa_circ_175688,RMVar_hsa_circ_96554,RMVar_hsa_circ_175691 17071 RMVar_ID_17071 Human_SNP_ID_591231603 A-to-I Human chr16 - 2222146 2222146 2222146 ACGATCTTGGTTCACTGCAATCTCCGCCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTG ACGATCTTGGTTCACTGCAATCTCCGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277980309 Functional Loss SNV dbSNP153 33..33 33 - - - 17072 RMVar_ID_17072 Human_SNP_ID_591232869 A-to-I Human chr16 + 2225630 2225630 2225630 TGAGTAGCTGGGATTACGGCACGCGGCATCACACCCGGCTAATTTTGCATTTTTAGTAGAGACTG TGAGTAGCTGGGATTACGGCACGCGGCATCACTCCCGGCTAATTTTGCATTTTTAGTAGAGACTG A T E4F1 Ensembl:ENSG00000167967 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1467473316 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5181006 17073 RMVar_ID_17073 Human_SNP_ID_591238643 A-to-I Human chr16 + 2240701 2240694 2240702 GCACACACATCCTGGCTAATTTTGTATTATTTATTTATTTATTTTTGAGATGGAGTCTGTCTCTG GCACACACATCCTGGCTAATTTTGTA________TTATTTATTTTTGAGATGGAGTCTGTCTCTG ATTATTTAT A AC009065.9 Ensembl:ENSG00000261663 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs889905068 Functional Loss DEL dbSNP153 27..34 33 - - - 17074 RMVar_ID_17074 Human_SNP_ID_591238644 A-to-I Human chr16 + 2240701 2240694 2240702 GCACACACATCCTGGCTAATTTTGTATTATTTATTTATTTATTTTTGAGATGGAGTCTGTCTCTG GCACACACATCCTGGCTAATTTTGTATTAT____TTATTTATTTTTGAGATGGAGTCTGTCTCTG ATTATTTAT ATTAT AC009065.9 Ensembl:ENSG00000261663 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs889905068 Functional Loss DEL dbSNP153 31..34 33 - - - 17075 RMVar_ID_17075 Human_SNP_ID_591243230 A-to-I Human chr16 - 2253453 2253453 2253453 CACACCCCCTCAAAGATCCTCTCACCCATGGTAGTTGCTGCTCGTGGTTCTGTCTGTCCGTGCAC CACACCCCCTCAAAGATCCTCTCACCCATGGTGGTTGCTGCTCGTGGTTCTGTCTGTCCGTGCAC T C RNPS1 Ensembl:ENSG00000205937 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1804278 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_470600,Human_RBP_ID_1514430,Human_RBP_ID_1839590,Human_RBP_ID_3492736,Human_RBP_ID_4356486,Human_RBP_ID_6500476,Human_RBP_ID_8429795,Human_RBP_ID_9060953,Human_RBP_ID_12690798,Human_RBP_ID_18675115,Human_RBP_ID_22497398,Human_RBP_ID_22800270,Human_RBP_ID_23682877,Human_RBP_ID_26439934,Human_RBP_ID_26809884,Human_RBP_ID_27238702 Human_miRNA_ID_2101507,Human_miRNA_ID_2107462,Human_miRNA_ID_2113404,Human_miRNA_ID_2165953,Human_miRNA_ID_2597200,Human_miRNA_ID_2740111,Human_miRNA_ID_3040704 RMVar_hsa_circ_377688,RMVar_hsa_circ_175728 17076 RMVar_ID_17076 Human_SNP_ID_591244281 A-to-I Human chr16 - 2256434 2256434 2256434 TTTGCCTCAGCCTCCCGAGTAGCTGCGATTACAGGCACACGCCACCACGCCCGGCTAATTTTTGT TTTGCCTCAGCCTCCCGAGTAGCTGCGATTACGGGCACACGCCACCACGCCCGGCTAATTTTTGT T C RNPS1 Ensembl:ENSG00000205937 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1205418575 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12690879 RMVar_hsa_circ_23291,RMVar_hsa_circ_30281 17077 RMVar_ID_17077 Human_SNP_ID_591261108 A-to-I Human chr16 - 2308578 2308578 2308578 AGCCTTCGGAGGCTTCCTCTACTTCTTCACCTACATCCCCTACTTCTTCGTGGCCCCTCGGTACA AGCCTTCGGAGGCTTCCTCTACTTCTTCACCTGCATCCCCTACTTCTTCGTGGCCCCTCGGTACA T C ABCA3 Ensembl:ENSG00000167972 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1427650233 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5630,Human_RBP_ID_45309,Human_RBP_ID_470899,Human_RBP_ID_4357296,Human_RBP_ID_8088580,Human_RBP_ID_8252010,Human_RBP_ID_17369154,Human_RBP_ID_17485653 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 17078 RMVar_ID_17078 Human_SNP_ID_591294992 A-to-I Human chr16 + 2431600 2431600 2431600 TACTAGGGAGGCTGAGGCGGGAAAATTGCTTGAACCTGGGAGGCAGAGCTTGCAGTGAGCCGAGA TACTAGGGAGGCTGAGGCGGGAAAATTGCTTGCACCTGGGAGGCAGAGCTTGCAGTGAGCCGAGA A C CCNF Ensembl:ENSG00000162063 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs150266909 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_30086,RMVar_hsa_circ_110860,RMVar_hsa_circ_373764,RMVar_hsa_circ_175752,RMVar_hsa_circ_107076,RMVar_hsa_circ_175753,RMVar_hsa_circ_175754 17079 RMVar_ID_17079 Human_SNP_ID_591294993 A-to-I Human chr16 + 2431600 2431600 2431600 TACTAGGGAGGCTGAGGCGGGAAAATTGCTTGAACCTGGGAGGCAGAGCTTGCAGTGAGCCGAGA TACTAGGGAGGCTGAGGCGGGAAAATTGCTTGGACCTGGGAGGCAGAGCTTGCAGTGAGCCGAGA A G CCNF Ensembl:ENSG00000162063 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs150266909 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_30086,RMVar_hsa_circ_110860,RMVar_hsa_circ_373764,RMVar_hsa_circ_175752,RMVar_hsa_circ_107076,RMVar_hsa_circ_175753,RMVar_hsa_circ_175754 17080 RMVar_ID_17080 Human_SNP_ID_591295132 A-to-I Human chr16 + 2432037 2432037 2432037 TATTTTTAGTAGAGTTGGGGTTTCACTGTGTTAGCCAGGATGGTCTCTATCTCTTGACCTCGTGA TATTTTTAGTAGAGTTGGGGTTTCACTGTGTTGGCCAGGATGGTCTCTATCTCTTGACCTCGTGA A G CCNF Ensembl:ENSG00000162063 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs946391927 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_30086,RMVar_hsa_circ_110860,RMVar_hsa_circ_373764,RMVar_hsa_circ_175752,RMVar_hsa_circ_107076,RMVar_hsa_circ_175753,RMVar_hsa_circ_175754 17081 RMVar_ID_17081 Human_SNP_ID_591300686 A-to-I Human chr16 + 2448532 2448532 2448532 GGGCTTAAGCAATCCTCCCACCTTAGCGTCCCAAGTAACTGAGACTATAGGCACGTGCCACCATG GGGCTTAAGCAATCCTCCCACCTTAGCGTCCCTAGTAACTGAGACTATAGGCACGTGCCACCATG A T CCNF Ensembl:ENSG00000162063 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1384761210 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7239,RMVar_hsa_circ_373764,RMVar_hsa_circ_107076,RMVar_hsa_circ_37774,RMVar_hsa_circ_127733,RMVar_hsa_circ_175753,RMVar_hsa_circ_175754,RMVar_hsa_circ_105577,RMVar_hsa_circ_175756,RMVar_hsa_circ_124682,RMVar_hsa_circ_175757,RMVar_hsa_circ_24425,RMVar_hsa_circ_175758,RMVar_hsa_circ_86735,RMVar_hsa_circ_114364,RMVar_hsa_circ_49625,RMVar_hsa_circ_175760,RMVar_hsa_circ_84544,RMVar_hsa_circ_175759,RMVar_hsa_circ_378969,RMVar_hsa_circ_175765,RMVar_hsa_circ_378998,RMVar_hsa_circ_18122 17082 RMVar_ID_17082 Human_SNP_ID_591306801 A-to-I Human chr16 - 2465621 2465621 2465621 TGGCTCACTGCAGGCTCAAAGTGCGAGGCTCAAGCGATCCTCCCGCCTTAGCCTCCCAAGTAGCT TGGCTCACTGCAGGCTCAAAGTGCGAGGCTCAGGCGATCCTCCCGCCTTAGCCTCCCAAGTAGCT T C AC106820.2 Ensembl:ENSG00000259895 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1342259631 Functional Loss SNV dbSNP153 33..33 33 - - - 17083 RMVar_ID_17083 Human_SNP_ID_591311482 A-to-I Human chr16 + 2480331 2480331 2480331 TTTTTATTTTTTTGTAGAGACAGTATCTTACTATGTTGCCCAGGCTGGTCTTGAACTCCTGGCTC TTTTTATTTTTTTGTAGAGACAGTATCTTACTCTGTTGCCCAGGCTGGTCTTGAACTCCTGGCTC A C AC106820.4,TBC1D24 Ensembl:ENSG00000260293,Ensembl:ENSG00000162065 lincRNA,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1415099896 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3510952,Human_RBP_ID_12703643,Human_RBP_ID_25201222 17084 RMVar_ID_17084 Human_SNP_ID_591322930 A-to-I Human chr16 - 2519022 2519022 2519022 ACAGCCACGGGCAAGCAAAAGGAGGCCAGGACAGCCACTCCTCCTTCCTCTACGTGAGGCCCCCA ACAGCCACGGGCAAGCAAAAGGAGGCCAGGACCGCCACTCCTCCTTCCTCTACGTGAGGCCCCCA T G - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1450712135 Functional Loss SNV dbSNP153 33..33 33 - - - 17085 RMVar_ID_17085 Human_SNP_ID_591324696 A-to-I Human chr16 + 2522217 2522217 2522217 GCGATCCTCTTGCTTCAGCCTCTTGAGTAGGTAGGACTACAGGTGTGTGCCACCATGCCCAGCCA GCGATCCTCTTGCTTCAGCCTCTTGAGTAGGTGGGACTACAGGTGTGTGCCACCATGCCCAGCCA A G AMDHD2,AC093525.1 Ensembl:ENSG00000162066,Ensembl:ENSG00000259784 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232894498 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12704030 RMVar_hsa_circ_175785,RMVar_hsa_circ_121525 17086 RMVar_ID_17086 Human_SNP_ID_591325746 A-to-I Human chr16 + 2525241 2525241 2525241 GCCATGCCCTGCTAATTTTTGTAATTTTTAGTAGAGATGGGCTTGCTCCATGTTGGCAAGGCTGG GCCATGCCCTGCTAATTTTTGTAATTTTTAGTGGAGATGGGCTTGCTCCATGTTGGCAAGGCTGG A G AMDHD2,AC093525.1 Ensembl:ENSG00000162066,Ensembl:ENSG00000259784 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1351151919 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12704123 RMVar_hsa_circ_175785,RMVar_hsa_circ_121525 17087 RMVar_ID_17087 Human_SNP_ID_591326250 A-to-I Human chr16 + 2526682 2526682 2526682 ACCGTTGGCCAGGCATGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGACTAAGGTGGGTGT ACCGTTGGCCAGGCATGGTGGCTCACGCCTGTGATCCCAGCACTTTGGGAGACTAAGGTGGGTGT A G AMDHD2,AC093525.1 Ensembl:ENSG00000162066,Ensembl:ENSG00000259784 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs955253332 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_175785,RMVar_hsa_circ_121525 17088 RMVar_ID_17088 Human_SNP_ID_591326280 A-to-I Human chr16 + 2526769 2526769 2526769 CCTGACCTACATGGTGAAACCCCGCCTCTACTAAAAATACAAAATTAGCCGAGCATGGTCGTGCA CCTGACCTACATGGTGAAACCCCGCCTCTACTGAAAATACAAAATTAGCCGAGCATGGTCGTGCA A G AMDHD2,AC093525.1 Ensembl:ENSG00000162066,Ensembl:ENSG00000259784 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1056460656 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_175785,RMVar_hsa_circ_121525 17089 RMVar_ID_17089 Human_SNP_ID_591338710 A-to-I Human chr16 - 2579789 2579789 2579789 GCCACCAGGCCCAGCTAATTTTTGTTACTTTTAGTAGAGACAGGGTCTCGCCACGTTGGCCATGC GCCACCAGGCCCAGCTAATTTTTGTTACTTTTGGTAGAGACAGGGTCTCGCCACGTTGGCCATGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1164300225 Functional Loss SNV dbSNP153 33..33 33 - - - 17090 RMVar_ID_17090 Human_SNP_ID_591340723 A-to-I Human chr16 + 2589549 2589549 2589549 GTCTCTACAAAAAATACAAAAATCAACCAGGCATGGTGCTGCACACCTGTAGTCCTAGCTGCTTG GTCTCTACAAAAAATACAAAAATCAACCAGGCGTGGTGCTGCACACCTGTAGTCCTAGCTGCTTG A G PDPK1 Ensembl:ENSG00000140992 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1488165420 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_366277,RMVar_hsa_circ_94355,RMVar_hsa_circ_118884,RMVar_hsa_circ_175796,RMVar_hsa_circ_175797 17091 RMVar_ID_17091 Human_SNP_ID_591383017 A-to-I Human chr16 - 2751226 2751226 2751226 ATTGGTCAGGCTGGTCTCGATTTCCTGACCTCAGGTGATCTGCCCACCTCAGCCTCCCAAAGTGC ATTGGTCAGGCTGGTCTCGATTTCCTGACCTCGGGTGATCTGCCCACCTCAGCCTCCCAAAGTGC T C SRRM2-AS1 Ensembl:ENSG00000205913 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs574226828 Functional Loss SNV dbSNP153 33..33 33 - - - 17092 RMVar_ID_17092 Human_SNP_ID_591387715 A-to-I Human chr16 + 2761579 2761579 2761579 TCTTCCACTCTTAGAAATCTGCAACTCGACCTAGCCCCTCTCCGGAAAGGAGCAGCACAGGCCCA TCTTCCACTCTTAGAAATCTGCAACTCGACCTGGCCCCTCTCCGGAAAGGAGCAGCACAGGCCCA A G SRRM2 Ensembl:ENSG00000167978 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs755950417 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_45323,Human_RBP_ID_818609,Human_RBP_ID_1515473,Human_RBP_ID_1840656,Human_RBP_ID_4359870,Human_RBP_ID_8430988,Human_RBP_ID_8806262,Human_RBP_ID_9372113,Human_RBP_ID_12708655,Human_RBP_ID_17253638,Human_RBP_ID_17369306,Human_RBP_ID_18411649,Human_RBP_ID_18676388,Human_RBP_ID_20109882,Human_RBP_ID_22199189,Human_RBP_ID_22800501,Human_RBP_ID_22945568,Human_RBP_ID_24544362,Human_RBP_ID_25202505,Human_RBP_ID_26328527,Human_RBP_ID_26440366,Human_RBP_ID_26941599,Human_RBP_ID_27239636 Human_Splice_Rec_1667118,Human_Splice_Rec_1667136,Human_Splice_Rec_1667156,Human_Splice_Rec_1667200,Human_Splice_Rec_1667224,Human_Splice_Rec_1667272,Human_Splice_Rec_1667276,Human_Splice_Rec_1667278 Human_miRNA_ID_2390744,Human_miRNA_ID_2591987 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 17093 RMVar_ID_17093 Human_SNP_ID_591387716 A-to-I Human chr16 + 2761579 2761579 2761579 TCTTCCACTCTTAGAAATCTGCAACTCGACCTAGCCCCTCTCCGGAAAGGAGCAGCACAGGCCCA TCTTCCACTCTTAGAAATCTGCAACTCGACCTTGCCCCTCTCCGGAAAGGAGCAGCACAGGCCCA A T SRRM2 Ensembl:ENSG00000167978 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs755950417 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_45323,Human_RBP_ID_818609,Human_RBP_ID_1515473,Human_RBP_ID_1840656,Human_RBP_ID_4359870,Human_RBP_ID_8430988,Human_RBP_ID_8806262,Human_RBP_ID_9372113,Human_RBP_ID_12708655,Human_RBP_ID_17253638,Human_RBP_ID_17369306,Human_RBP_ID_18411649,Human_RBP_ID_18676388,Human_RBP_ID_20109882,Human_RBP_ID_22199189,Human_RBP_ID_22800501,Human_RBP_ID_22945568,Human_RBP_ID_24544362,Human_RBP_ID_25202505,Human_RBP_ID_26328527,Human_RBP_ID_26440366,Human_RBP_ID_26941599,Human_RBP_ID_27239636 Human_Splice_Rec_1667118,Human_Splice_Rec_1667136,Human_Splice_Rec_1667156,Human_Splice_Rec_1667200,Human_Splice_Rec_1667224,Human_Splice_Rec_1667272,Human_Splice_Rec_1667276,Human_Splice_Rec_1667278 Human_miRNA_ID_2390744,Human_miRNA_ID_2591987 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 17094 RMVar_ID_17094 Human_SNP_ID_591390037 A-to-I Human chr16 + 2765401 2765401 2765401 CACAGAGTGGTTCTGATTCCTCTCCTGAACCTAAAGCTCCAGCCCCTCGGGCCCTTCCCAGACGA CACAGAGTGGTTCTGATTCCTCTCCTGAACCTGAAGCTCCAGCCCCTCGGGCCCTTCCCAGACGA A G SRRM2 Ensembl:ENSG00000167978 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1209925932 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_45336,Human_RBP_ID_1515616,Human_RBP_ID_1840755,Human_RBP_ID_8431135,Human_RBP_ID_8806463,Human_RBP_ID_17253707,Human_RBP_ID_18676560,Human_RBP_ID_22199268,Human_RBP_ID_22497552,Human_RBP_ID_22800560,Human_RBP_ID_26941719,Human_RBP_ID_27447915 Human_miRNA_ID_2390745,Human_miRNA_ID_2591988 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 17095 RMVar_ID_17095 Human_SNP_ID_591391392 A-to-I Human chr16 + 2767714 2767714 2767714 TGCCCCTTTCTGCCTACGAGCGTGTCAGTGGCAGAACCTCACCACCGCTCCTTGACCGAGCTAGG TGCCCCTTTCTGCCTACGAGCGTGTCAGTGGCGGAACCTCACCACCGCTCCTTGACCGAGCTAGG A G SRRM2 Ensembl:ENSG00000167978 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1357971733 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1515726,Human_RBP_ID_1840854,Human_RBP_ID_8806567,Human_RBP_ID_12710280,Human_RBP_ID_17253754,Human_RBP_ID_18437422,Human_RBP_ID_18676687,Human_RBP_ID_27239752,Human_RBP_ID_27440896 Human_miRNA_ID_2007408 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 17096 RMVar_ID_17096 Human_SNP_ID_591429780 A-to-I Human chr16 + 2884619 2884619 2884619 TAGTCGGGGCCGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGAGGGTGG TAGTCGGGGCCGGCGCGGTGGCTCACGCCTGTTATCCCAGCACTTTGGGAGGCCAAGGAGGGTGG A T FLYWCH2 Ensembl:ENSG00000162076 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277611854 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81103,RMVar_hsa_circ_175831 17097 RMVar_ID_17097 Human_SNP_ID_591430653 A-to-I Human chr16 + 2887169 2887169 2887169 TATAATTTTTTGTTTTTTTGTTGTTTTGAGACAGGATCTCACTCTGTTACCCAAGCTGGAGTGCA TATAATTTTTTGTTTTTTTGTTGTTTTGAGACGGGATCTCACTCTGTTACCCAAGCTGGAGTGCA A G FLYWCH2 Ensembl:ENSG00000162076 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1567302752 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12713697 RMVar_hsa_circ_81103,RMVar_hsa_circ_175831 17098 RMVar_ID_17098 Human_SNP_ID_591432556 A-to-I Human chr16 + 2892723 2892723 2892723 AAAATTAGGAGAGCATGGTGGCGTGTGCCTGTAGTCCCAGCTATGTGGGAGGCTGAGGCAGGAGG AAAATTAGGAGAGCATGGTGGCGTGTGCCTGTGGTCCCAGCTATGTGGGAGGCTGAGGCAGGAGG A G FLYWCH2 Ensembl:ENSG00000162076 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1243089101 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81103,RMVar_hsa_circ_175831 17099 RMVar_ID_17099 Human_SNP_ID_591435075 A-to-I Human chr16 + 2899938 2899936 2899938 CAGGCTGGAGTGCAGTGGCACGATCTGGACTCACTGCAACCACCACCTCCCGGGTTCAAGCGATT CAGGCTGGAGTGCAGTGGCACGATCTGGACT__CTGCAACCACCACCTCCCGGGTTCAAGCGATT TCA T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1330537874 Functional Loss DEL dbSNP153 32..33 33 - - - 17100 RMVar_ID_17100 Human_SNP_ID_591435078 A-to-I Human chr16 + 2899943 2899943 2899943 TGGAGTGCAGTGGCACGATCTGGACTCACTGCAACCACCACCTCCCGGGTTCAAGCGATTCTCTT TGGAGTGCAGTGGCACGATCTGGACTCACTGCCACCACCACCTCCCGGGTTCAAGCGATTCTCTT A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1001572318 Functional Loss SNV dbSNP153 33..33 33 - - - 17101 RMVar_ID_17101 Human_SNP_ID_591435164 A-to-I Human chr16 + 2900256 2900256 2900256 TTTTTTGTTCGTTTGTTTTGTTTTGTTTTTTGAGATGGGGTCTCACTCTGTAGCCCAGGCTGGAG TTTTTTGTTCGTTTGTTTTGTTTTGTTTTTTGCGATGGGGTCTCACTCTGTAGCCCAGGCTGGAG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs952761212 Functional Loss SNV dbSNP153 33..33 33 - - - 17102 RMVar_ID_17102 Human_SNP_ID_591435165 A-to-I Human chr16 + 2900268 2900268 2900268 TTGTTTTGTTTTGTTTTTTGAGATGGGGTCTCACTCTGTAGCCCAGGCTGGAGTGCAGTGGTGTG TTGTTTTGTTTTGTTTTTTGAGATGGGGTCTCGCTCTGTAGCCCAGGCTGGAGTGCAGTGGTGTG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1418197875 Functional Loss SNV dbSNP153 33..33 33 - - - 17103 RMVar_ID_17103 Human_SNP_ID_591435212 A-to-I Human chr16 + 2900445 2900445 2900445 TTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGTTGGTCTGGAACTCTGGACCTCAGGTGATC TTTAGTAGAGATGGGGTTTCACCATGTTGGCCGGGTTGGTCTGGAACTCTGGACCTCAGGTGATC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1449510911 Functional Loss SNV dbSNP153 33..33 33 - - - 17104 RMVar_ID_17104 Human_SNP_ID_591437297 A-to-I Human chr16 + 2906427 2906427 2906427 GAGGTCGGAAGTTAGAGAGCAGCCTGACCAACATGGAGAAACTCAGACTCTACTAAAAATCCAAA GAGGTCGGAAGTTAGAGAGCAGCCTGACCAACGTGGAGAAACTCAGACTCTACTAAAAATCCAAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1421722945 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8431664 17105 RMVar_ID_17105 Human_SNP_ID_591437304 A-to-I Human chr16 + 2906449 2906448 2906449 CCTGACCAACATGGAGAAACTCAGACTCTACTAAAAATCCAAAACTAGCCGGGCGTGGTGGCGCA CCTGACCAACATGGAGAAACTCAGACTCTACT_AAAATCCAAAACTAGCCGGGCGTGGTGGCGCA TA T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs981572879 Functional Loss DEL dbSNP153 33..33 33 - - - 17106 RMVar_ID_17106 Human_SNP_ID_591437305 A-to-I Human chr16 + 2906449 2906449 2906449 CCTGACCAACATGGAGAAACTCAGACTCTACTAAAAATCCAAAACTAGCCGGGCGTGGTGGCGCA CCTGACCAACATGGAGAAACTCAGACTCTACTGAAAATCCAAAACTAGCCGGGCGTGGTGGCGCA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1475193421 Functional Loss SNV dbSNP153 33..33 33 - - - 17107 RMVar_ID_17107 Human_SNP_ID_591442102 A-to-I Human chr16 + 2920274 2920274 2920274 GTTTAGTAGAGCACCTGTAATCCCAGCACTTTAGGAGGCAGGTAGGTAACTAGAGGCCAGGAGTT GTTTAGTAGAGCACCTGTAATCCCAGCACTTTGGGAGGCAGGTAGGTAACTAGAGGCCAGGAGTT A G FLYWCH1 Ensembl:ENSG00000059122 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1313026723 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22370 17108 RMVar_ID_17108 Human_SNP_ID_591451369 A-to-I Human chr16 + 2940988 2940988 2940988 CCCCATCTCTACTAAAAATACAAAAATTAGTCAGGCATGGTGGTACATGCATGTAATCCAAGCTA CCCCATCTCTACTAAAAATACAAAAATTAGTCGGGCATGGTGGTACATGCATGTAATCCAAGCTA A G FLYWCH1 Ensembl:ENSG00000059122 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1235522566 Functional Loss SNV dbSNP153 33..33 33 - - - 17109 RMVar_ID_17109 Human_SNP_ID_591452680 A-to-I Human chr16 + 2944210 2944210 2944210 GGAATTCCAGACCAGCCTGGGGAACATGGAGAAACTCCGTCTCTACTAAAAATACAATAGCCAGG GGAATTCCAGACCAGCCTGGGGAACATGGAGAGACTCCGTCTCTACTAAAAATACAATAGCCAGG A G FLYWCH1 Ensembl:ENSG00000059122 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs150822314 Functional Loss SNV dbSNP153 33..33 33 - - - 17110 RMVar_ID_17110 Human_SNP_ID_591465834 A-to-I Human chr16 - 2978661 2978661 2978661 TCACTGTAATCTCTGCCTCCCAGGTTCAAGCAATTCCCCTGCCTCAGCCTCCCGAGTAGCTGGGA TCACTGTAATCTCTGCCTCCCAGGTTCAAGCAGTTCCCCTGCCTCAGCCTCCCGAGTAGCTGGGA T C PKMYT1 Ensembl:ENSG00000127564 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1001328420 Functional Loss SNV dbSNP153 33..33 33 - - - 17111 RMVar_ID_17111 Human_SNP_ID_591465835 A-to-I Human chr16 - 2978662 2978662 2978662 CTCACTGTAATCTCTGCCTCCCAGGTTCAAGCAATTCCCCTGCCTCAGCCTCCCGAGTAGCTGGG CTCACTGTAATCTCTGCCTCCCAGGTTCAAGCTATTCCCCTGCCTCAGCCTCCCGAGTAGCTGGG T A PKMYT1 Ensembl:ENSG00000127564 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1032353064 Functional Loss SNV dbSNP153 33..33 33 - - - 17112 RMVar_ID_17112 Human_SNP_ID_591465837 A-to-I Human chr16 - 2978665 2978665 2978665 TGGCTCACTGTAATCTCTGCCTCCCAGGTTCAAGCAATTCCCCTGCCTCAGCCTCCCGAGTAGCT TGGCTCACTGTAATCTCTGCCTCCCAGGTTCATGCAATTCCCCTGCCTCAGCCTCCCGAGTAGCT T A PKMYT1 Ensembl:ENSG00000127564 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1352186182 Functional Loss SNV dbSNP153 33..33 33 - - - 17113 RMVar_ID_17113 Human_SNP_ID_591465908 A-to-I Human chr16 - 2978867 2978866 2978868 GGGAGTCGGAGGCTGCAGTGGGCCGAGATCATACCACTGCACTCCAGCCTGGGCAACAGAGTGAG GGGAGTCGGAGGCTGCAGTGGGCCGAGATCA__CCACTGCACTCCAGCCTGGGCAACAGAGTGAG GTA G PKMYT1 Ensembl:ENSG00000127564 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335580043 Functional Loss DEL dbSNP153 32..33 33 - - - 17114 RMVar_ID_17114 Human_SNP_ID_591465923 A-to-I Human chr16 - 2978909 2978909 2978909 CCAGCTACTCAGGAGGCTGAGGCAAGAGAATTACTTGAACCTGGGAGTCGGAGGCTGCAGTGGGC CCAGCTACTCAGGAGGCTGAGGCAAGAGAATTCCTTGAACCTGGGAGTCGGAGGCTGCAGTGGGC T G PKMYT1 Ensembl:ENSG00000127564 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1368567023 Functional Loss SNV dbSNP153 33..33 33 - - - 17115 RMVar_ID_17115 Human_SNP_ID_591465929 A-to-I Human chr16 - 2978944 2978944 2978944 AAATTATTCTAGTGTGTTGGCACACGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAAGAGAA AAATTATTCTAGTGTGTTGGCACACGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAAGAGAA T C PKMYT1 Ensembl:ENSG00000127564 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049601738 Functional Loss SNV dbSNP153 33..33 33 - - - 17116 RMVar_ID_17116 Human_SNP_ID_591479679 A-to-I Human chr16 + 3022034 3022034 3022034 GTCTGGTTGCCCTGCCTCTGGCTCCAGAACAGAAAGGGAGCCTCACGCTGGCTCACACAAAACAG GTCTGGTTGCCCTGCCTCTGGCTCCAGAACAGCAAGGGAGCCTCACGCTGGCTCACACAAAACAG A C TNFRSF12A Ensembl:ENSG00000006327 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982728031 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8186806,Human_RBP_ID_8432306,Human_RBP_ID_26329716 Human_miRNA_ID_543872,Human_miRNA_ID_579105 17117 RMVar_ID_17117 Human_SNP_ID_591479920 A-to-I Human chr16 - 3022767 3022767 3022767 CCGCAAAGGGACAAGGTTCCTCCCTCTCCTGCAGAGTAGGCATCTGGGCACCAAGACCTTCCCTC CCGCAAAGGGACAAGGTTCCTCCCTCTCCTGCGGAGTAGGCATCTGGGCACCAAGACCTTCCCTC T C HCFC1R1 Ensembl:ENSG00000103145 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs11558419 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1516836,Human_RBP_ID_5419225,Human_RBP_ID_26809924 RMVar_hsa_circ_175835,RMVar_hsa_circ_127819 17118 RMVar_ID_17118 Human_SNP_ID_591518099 A-to-I Human chr16 - 3129701 3129700 3129702 TAAGCTTTGTCAGTAGAGGGCGCTGGAGAGACATTGCAGGAGACGAGTTTCCCTTCCTGCTTCTG TAAGCTTTGTCAGTAGAGGGCGCTGGAGAGA__TTGCAGGAGACGAGTTTCCCTTCCTGCTTCTG ATG A ZNF213-AS1 Ensembl:ENSG00000263072 lincRNA intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1377010362 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_12727212 RMVar_hsa_circ_289953 17119 RMVar_ID_17119 Human_SNP_ID_591518100 A-to-I Human chr16 - 3129701 3129701 3129701 TAAGCTTTGTCAGTAGAGGGCGCTGGAGAGACATTGCAGGAGACGAGTTTCCCTTCCTGCTTCTG TAAGCTTTGTCAGTAGAGGGCGCTGGAGAGACGTTGCAGGAGACGAGTTTCCCTTCCTGCTTCTG T C ZNF213-AS1 Ensembl:ENSG00000263072 lincRNA intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs930556380 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12727212 RMVar_hsa_circ_289953 17120 RMVar_ID_17120 Human_SNP_ID_591518360 A-to-I Human chr16 - 3130472 3130467 3130472 GGTGAAACCCCAGCTCTACTAAAAATACAAAAAATAAGCCGGACGTGGTGGCAGGCACCTTGTCC GGTGAAACCCCAGCTCTACTAAAAATACAAAA_____GCCGGACGTGGTGGCAGGCACCTTGTCC CTTATT C ZNF213-AS1 Ensembl:ENSG00000263072 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1312963087 Functional Loss DEL dbSNP153 33..37 33 - - - RMVar_hsa_circ_289953 17121 RMVar_ID_17121 Human_SNP_ID_591518362 A-to-I Human chr16 - 3130472 3130472 3130472 GGTGAAACCCCAGCTCTACTAAAAATACAAAAAATAAGCCGGACGTGGTGGCAGGCACCTTGTCC GGTGAAACCCCAGCTCTACTAAAAATACAAAACATAAGCCGGACGTGGTGGCAGGCACCTTGTCC T G ZNF213-AS1 Ensembl:ENSG00000263072 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1353954514 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_289953 17122 RMVar_ID_17122 Human_SNP_ID_591518363 A-to-I Human chr16 - 3130475 3130475 3130475 CACGGTGAAACCCCAGCTCTACTAAAAATACAAAAAATAAGCCGGACGTGGTGGCAGGCACCTTG CACGGTGAAACCCCAGCTCTACTAAAAATACAGAAAATAAGCCGGACGTGGTGGCAGGCACCTTG T C ZNF213-AS1 Ensembl:ENSG00000263072 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs976288185 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_289953 17123 RMVar_ID_17123 Human_SNP_ID_591568531 A-to-I Human chr16 + 3268963 3268963 3268963 TACTAAGTAGGCTGAGGCGGGAGGATCGATTGAAGCCGGGAGGTGGAGGTTGCAGTGAGCCGAGA TACTAAGTAGGCTGAGGCGGGAGGATCGATTGCAGCCGGGAGGTGGAGGTTGCAGTGAGCCGAGA A C ZNF263 Ensembl:ENSG00000006194 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1345096224 Functional Loss SNV dbSNP153 33..33 33 - - - 17124 RMVar_ID_17124 Human_SNP_ID_591569849 A-to-I Human chr16 + 3272240 3272240 3272240 AGGCATGGTGGCACGTGCCTGTAGTCTCAGCTACTCGCGAGGCTGAGGCAGAAGAATTGCTTGAA AGGCATGGTGGCACGTGCCTGTAGTCTCAGCTGCTCGCGAGGCTGAGGCAGAAGAATTGCTTGAA A G ZNF263 Ensembl:ENSG00000006194 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1394343033 Functional Loss SNV dbSNP153 33..33 33 - - - 17125 RMVar_ID_17125 Human_SNP_ID_591572458 A-to-I Human chr16 - 3281967 3281967 3281967 AAATTCCTCACCTCGAGTGATCTGCCCGCCTTAGCCTCCCACTGTGCTGGGATTACAGGCGTGAG AAATTCCTCACCTCGAGTGATCTGCCCGCCTTTGCCTCCCACTGTGCTGGGATTACAGGCGTGAG T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1044398251 Functional Loss SNV dbSNP153 33..33 33 - - - 17126 RMVar_ID_17126 Human_SNP_ID_591572459 A-to-I Human chr16 - 3281967 3281967 3281967 AAATTCCTCACCTCGAGTGATCTGCCCGCCTTAGCCTCCCACTGTGCTGGGATTACAGGCGTGAG AAATTCCTCACCTCGAGTGATCTGCCCGCCTTGGCCTCCCACTGTGCTGGGATTACAGGCGTGAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1044398251 Functional Loss SNV dbSNP153 33..33 33 - - - 17127 RMVar_ID_17127 Human_SNP_ID_591580287 A-to-I Human chr16 + 3306550 3306550 3306550 CCTGGCCAAGATGGTGAAACCCTGTCTCTACTAAAAACACAAAAATTAGCCGGGCATGGTGGCAC CCTGGCCAAGATGGTGAAACCCTGTCTCTACTGAAAACACAAAAATTAGCCGGGCATGGTGGCAC A G ZNF75A Ensembl:ENSG00000162086 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1386908895 Functional Loss SNV dbSNP153 33..33 33 - - - 17128 RMVar_ID_17128 Human_SNP_ID_591580295 A-to-I Human chr16 + 3306573 3306573 3306573 GTCTCTACTAAAAACACAAAAATTAGCCGGGCATGGTGGCACGCGCCTGTAATCCCAGCTAGTCG GTCTCTACTAAAAACACAAAAATTAGCCGGGCGTGGTGGCACGCGCCTGTAATCCCAGCTAGTCG A G ZNF75A Ensembl:ENSG00000162086 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs147922947 Functional Loss SNV dbSNP153 33..33 33 - - - 17129 RMVar_ID_17129 Human_SNP_ID_591580505 A-to-I Human chr16 + 3307091 3307091 3307091 TTCCTGCCTCAGCCTCCTGGGTAGCTGGGACTACAGGCGCGCACTACCACACCTGGCTAATTTTT TTCCTGCCTCAGCCTCCTGGGTAGCTGGGACTCCAGGCGCGCACTACCACACCTGGCTAATTTTT A C ZNF75A Ensembl:ENSG00000162086 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1344850788 Functional Loss SNV dbSNP153 33..33 33 - - - 17130 RMVar_ID_17130 Human_SNP_ID_591581558 A-to-I Human chr16 + 3310273 3310273 3310273 TAAACTAGCTGAGCATGGTGGCGTGTGCCCGTAATCCCAGCTACTCAGAAGGCTGAGGCAGGAGA TAAACTAGCTGAGCATGGTGGCGTGTGCCCGTCATCCCAGCTACTCAGAAGGCTGAGGCAGGAGA A C ZNF75A Ensembl:ENSG00000162086 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs138755970 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_175846,RMVar_hsa_circ_296235,RMVar_hsa_circ_340815 17131 RMVar_ID_17131 Human_SNP_ID_591606729 A-to-I Human chr16 - 3391855 3391855 3391855 GGCATCATAGTTCACTGCTGCCTCAAACTGCTAGGTTCAAGCAGTCCTCCTGCCTCAGCCTCCCA GGCATCATAGTTCACTGCTGCCTCAAACTGCTGGGTTCAAGCAGTCCTCCTGCCTCAGCCTCCCA T C ZSCAN32 Ensembl:ENSG00000140987 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs986767482 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29572 17132 RMVar_ID_17132 Human_SNP_ID_591635109 A-to-I Human chr16 + 3481247 3481247 3481247 TCTCAAGTAGGATTTTAGACGTGCGCCACCACACCAAGCTAATTTTTGTATTTTTAGTGGAGATG TCTCAAGTAGGATTTTAGACGTGCGCCACCACGCCAAGCTAATTTTTGTATTTTTAGTGGAGATG A G NAA60,AC004224.2 Ensembl:ENSG00000122390,Ensembl:ENSG00000263212 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs946496326 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_327003,RMVar_hsa_circ_364040,RMVar_hsa_circ_365503 17133 RMVar_ID_17133 Human_SNP_ID_591642761 A-to-I Human chr16 + 3503051 3503051 3503051 TCTCCCAGGCTGGAGTGCAGTGGTGTGATCTTAGCTCACTGCAACCTCTGCCTCCCAGCAATTCT TCTCCCAGGCTGGAGTGCAGTGGTGTGATCTTCGCTCACTGCAACCTCTGCCTCCCAGCAATTCT A C CLUAP1,AC004224.2 Ensembl:ENSG00000103351,Ensembl:ENSG00000263212 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1239908876 Functional Loss SNV dbSNP153 33..33 33 - - - 17134 RMVar_ID_17134 Human_SNP_ID_591664226 A-to-I Human chr16 - 3571476 3571476 3571476 GCAGTGGCACAATCATAGCTCACTGCAGCCTCAGCCTCCTGAGCTCAAGGGGTCCTCCTACCTCA GCAGTGGCACAATCATAGCTCACTGCAGCCTCGGCCTCCTGAGCTCAAGGGGTCCTCCTACCTCA T C NLRC3 Ensembl:ENSG00000167984 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1458872159 Functional Loss SNV dbSNP153 33..33 33 - - - 17135 RMVar_ID_17135 Human_SNP_ID_591664715 A-to-I Human chr16 - 3573315 3573315 3573315 TAAGCGATCCTCCCACCTCAGCTTCCTTGAGTAGCTGGGATTACAGGCATGCGCCACCGTGCTCA TAAGCGATCCTCCCACCTCAGCTTCCTTGAGTTGCTGGGATTACAGGCATGCGCCACCGTGCTCA T A NLRC3 Ensembl:ENSG00000167984 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs951474338 Functional Loss SNV dbSNP153 33..33 33 - - - 17136 RMVar_ID_17136 Human_SNP_ID_591665022 A-to-I Human chr16 - 3574280 3574280 3574280 ATTTAAAAGCCGTGCTCCACAAGGCCGGGCGCAGTGGTTCACACCTGTAATCCCAGCACTTTTGG ATTTAAAAGCCGTGCTCCACAAGGCCGGGCGCGGTGGTTCACACCTGTAATCCCAGCACTTTTGG T C NLRC3 Ensembl:ENSG00000167984 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1421316475 Functional Loss SNV dbSNP153 33..33 33 - - - 17137 RMVar_ID_17137 Human_SNP_ID_591665765 A-to-I Human chr16 - 3576697 3576695 3576697 GATCGAGCCACTGCACTCAATCCTGGGTGACAAAGCGAGACTGTCTCCAAAACAAAACAAAACAA GATCGAGCCACTGCACTCAATCCTGGGTGACA__GCGAGACTGTCTCCAAAACAAAACAAAACAA CTT C NLRC3 Ensembl:ENSG00000167984 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1453700165 Functional Loss DEL dbSNP153 33..34 33 - - - 17138 RMVar_ID_17138 Human_SNP_ID_591670744 A-to-I Human chr16 - 3591110 3591110 3591110 TTTGTTGAAATCCAAGGACCACGAAGAAGATCAAGAAAACGTGAATGAAGCAGAAATGGAAGAAA TTTGTTGAAATCCAAGGACCACGAAGAAGATCCAGAAAACGTGAATGAAGCAGAAATGGAAGAAA T G SLX4 Ensembl:ENSG00000188827 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs762300440 Functional Loss SNV dbSNP153 33..33 33 - - - 17139 RMVar_ID_17139 Human_SNP_ID_591675192 A-to-I Human chr16 - 3605120 3605120 3605120 GCACCACTGCACTCCAGCCTGGGCAACAGAGCAAGACTCTGACTCAAAAAAAAATTTTTTTTTAA GCACCACTGCACTCCAGCCTGGGCAACAGAGCGAGACTCTGACTCAAAAAAAAATTTTTTTTTAA T C SLX4 Ensembl:ENSG00000188827 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs544530096 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19593 17140 RMVar_ID_17140 Human_SNP_ID_591675197 A-to-I Human chr16 - 3605125 3605125 3605125 AGATTGCACCACTGCACTCCAGCCTGGGCAACAGAGCAAGACTCTGACTCAAAAAAAAATTTTTT AGATTGCACCACTGCACTCCAGCCTGGGCAACGGAGCAAGACTCTGACTCAAAAAAAAATTTTTT T C SLX4 Ensembl:ENSG00000188827 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1378550724 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19593 17141 RMVar_ID_17141 Human_SNP_ID_591675517 A-to-I Human chr16 - 3606112 3606112 3606112 GGGATTACAGACGTGTGCCACCACACCTGGCCAATTTTTGTATTTTTAGTAGAGACAGGGTTTCG GGGATTACAGACGTGTGCCACCACACCTGGCCCATTTTTGTATTTTTAGTAGAGACAGGGTTTCG T G SLX4 Ensembl:ENSG00000188827 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs908495100 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19593 17142 RMVar_ID_17142 Human_SNP_ID_591680421 A-to-I Human chr16 + 3620387 3620386 3620388 TAAAGAAACCTTTTATTTATTTATTTAGAGACAGAGTACTCAGTGTGTCACCCAGGCTGGAGTGC TAAAGAAACCTTTTATTTATTTATTTAGAGAC__AGTACTCAGTGTGTCACCCAGGCTGGAGTGC CAG C DNASE1 Ensembl:ENSG00000213918 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1180779090 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_6511514 17143 RMVar_ID_17143 Human_SNP_ID_591682192 A-to-I Human chr16 + 3625548 3625548 3625548 TTCAGTAGGCTGAAATGGGATCGCTTGAGCCCAGGAGGTCGAGGCTGCAGTGAATCATAATCGCC TTCAGTAGGCTGAAATGGGATCGCTTGAGCCCGGGAGGTCGAGGCTGCAGTGAATCATAATCGCC A G DNASE1 Ensembl:ENSG00000213918 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs777471721 Functional Loss SNV dbSNP153 33..33 33 - - - 17144 RMVar_ID_17144 Human_SNP_ID_591694092 A-to-I Human chr16 + 3659817 3659817 3659817 TCACTCCTTCACCCAAGCTAGAGTGAAATGGCATGATCTTGGCTCACCGCAGCCTCCTGGTTTCA TCACTCCTTCACCCAAGCTAGAGTGAAATGGCGTGATCTTGGCTCACCGCAGCCTCCTGGTTTCA A G DNASE1 Ensembl:ENSG00000213918 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs948259708 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_175895 17145 RMVar_ID_17145 Human_SNP_ID_591694109 A-to-I Human chr16 + 3659867 3659867 3659867 AGCCTCCTGGTTTCAAGAGGTTCTCTTGCCTCAGCCTCCCAAGTAACTGGGATTACAGGCACCCA AGCCTCCTGGTTTCAAGAGGTTCTCTTGCCTCGGCCTCCCAAGTAACTGGGATTACAGGCACCCA A G DNASE1 Ensembl:ENSG00000213918 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs754201370 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_175895 17146 RMVar_ID_17146 Human_SNP_ID_591694462 A-to-I Human chr16 + 3660790 3660790 3660790 AAAGAACAAAACAAAAACTGGCTGGGGGTGGTAGCCCACACTTGTAATCCCAGCACTTCGGGAGG AAAGAACAAAACAAAAACTGGCTGGGGGTGGTGGCCCACACTTGTAATCCCAGCACTTCGGGAGG A G DNASE1 Ensembl:ENSG00000213918 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1044216209 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_175895 17147 RMVar_ID_17147 Human_SNP_ID_591694468 A-to-I Human chr16 + 3660803 3660803 3660803 AAAACTGGCTGGGGGTGGTAGCCCACACTTGTAATCCCAGCACTTCGGGAGGCTAAGGCAGGTGG AAAACTGGCTGGGGGTGGTAGCCCACACTTGTCATCCCAGCACTTCGGGAGGCTAAGGCAGGTGG A C DNASE1 Ensembl:ENSG00000213918 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs796677577 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_175895 17148 RMVar_ID_17148 Human_SNP_ID_591697239 A-to-I Human chr16 - 3667389 3667389 3667389 AAACTCCTGACCTCTGGTGATCCGCCCGCCTCAGCCTCCCAAAGTGGTGCGATTACAGGCAGGAG AAACTCCTGACCTCTGGTGATCCGCCCGCCTCGGCCTCCCAAAGTGGTGCGATTACAGGCAGGAG T C TRAP1 Ensembl:ENSG00000126602 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1490966617 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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,RMVar_hsa_circ_175901,RMVar_hsa_circ_112563 17149 RMVar_ID_17149 Human_SNP_ID_591697506 A-to-I Human chr16 - 3668076 3668076 3668076 AAAAACACAAAATTTTAGCCAGTCGTGGTGGCAGGCAGGTGTAATCCCAGCCACTCGGGAGGCTG AAAAACACAAAATTTTAGCCAGTCGTGGTGGCGGGCAGGTGTAATCCCAGCCACTCGGGAGGCTG T C TRAP1 Ensembl:ENSG00000126602 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1275338046 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12730224 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_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,RMVar_hsa_circ_175901,RMVar_hsa_circ_112563 17150 RMVar_ID_17150 Human_SNP_ID_591701829 A-to-I Human chr16 - 3678569 3678569 3678569 ATCCCAGCTACTCGGGAGGCTGAGGCGGGAGAATCACTTGAACCCGGGAGGCAGAGGTTGCAGTG ATCCCAGCTACTCGGGAGGCTGAGGCGGGAGAGTCACTTGAACCCGGGAGGCAGAGGTTGCAGTG T C TRAP1 Ensembl:ENSG00000126602 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs917633288 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25244337 RMVar_hsa_circ_127986,RMVar_hsa_circ_126602,RMVar_hsa_circ_116781,RMVar_hsa_circ_104500,RMVar_hsa_circ_175884,RMVar_hsa_circ_175882,RMVar_hsa_circ_175883,RMVar_hsa_circ_175881,RMVar_hsa_circ_15167,RMVar_hsa_circ_65550,RMVar_hsa_circ_348350,RMVar_hsa_circ_83997,RMVar_hsa_circ_175900,RMVar_hsa_circ_80162,RMVar_hsa_circ_175899,RMVar_hsa_circ_22410,RMVar_hsa_circ_29280,RMVar_hsa_circ_89865,RMVar_hsa_circ_121533,RMVar_hsa_circ_334166,RMVar_hsa_circ_175902,RMVar_hsa_circ_175903,RMVar_hsa_circ_332212,RMVar_hsa_circ_323780,RMVar_hsa_circ_175904,RMVar_hsa_circ_332011,RMVar_hsa_circ_118776,RMVar_hsa_circ_102397,RMVar_hsa_circ_175909,RMVar_hsa_circ_175910,RMVar_hsa_circ_22841,RMVar_hsa_circ_31908,RMVar_hsa_circ_284963,RMVar_hsa_circ_291311,RMVar_hsa_circ_175911,RMVar_hsa_circ_329516,RMVar_hsa_circ_45423 17151 RMVar_ID_17151 Human_SNP_ID_591701840 A-to-I Human chr16 - 3678608 3678608 3678608 AAATACAAAAATTAGCTGGGCGTGGTGGTGGTACCTGTCATCCCAGCTACTCGGGAGGCTGAGGC AAATACAAAAATTAGCTGGGCGTGGTGGTGGTGCCTGTCATCCCAGCTACTCGGGAGGCTGAGGC T C TRAP1 Ensembl:ENSG00000126602 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1046958587 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127986,RMVar_hsa_circ_126602,RMVar_hsa_circ_116781,RMVar_hsa_circ_104500,RMVar_hsa_circ_175884,RMVar_hsa_circ_175882,RMVar_hsa_circ_175883,RMVar_hsa_circ_175881,RMVar_hsa_circ_15167,RMVar_hsa_circ_65550,RMVar_hsa_circ_348350,RMVar_hsa_circ_83997,RMVar_hsa_circ_175900,RMVar_hsa_circ_80162,RMVar_hsa_circ_175899,RMVar_hsa_circ_22410,RMVar_hsa_circ_29280,RMVar_hsa_circ_89865,RMVar_hsa_circ_121533,RMVar_hsa_circ_334166,RMVar_hsa_circ_175902,RMVar_hsa_circ_175903,RMVar_hsa_circ_332212,RMVar_hsa_circ_323780,RMVar_hsa_circ_175904,RMVar_hsa_circ_332011,RMVar_hsa_circ_118776,RMVar_hsa_circ_102397,RMVar_hsa_circ_175909,RMVar_hsa_circ_175910,RMVar_hsa_circ_22841,RMVar_hsa_circ_31908,RMVar_hsa_circ_284963,RMVar_hsa_circ_291311,RMVar_hsa_circ_175911,RMVar_hsa_circ_329516,RMVar_hsa_circ_45423 17152 RMVar_ID_17152 Human_SNP_ID_591701851 A-to-I Human chr16 - 3678633 3678633 3678633 CACGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCTGGGCGTGGTGGTGGTACCTGTCA CACGGTGAAACCCCGTCTCTACTAAAAATACAGAAATTAGCTGGGCGTGGTGGTGGTACCTGTCA T C TRAP1 Ensembl:ENSG00000126602 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1194362652 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127986,RMVar_hsa_circ_126602,RMVar_hsa_circ_116781,RMVar_hsa_circ_104500,RMVar_hsa_circ_175884,RMVar_hsa_circ_175882,RMVar_hsa_circ_175883,RMVar_hsa_circ_175881,RMVar_hsa_circ_15167,RMVar_hsa_circ_65550,RMVar_hsa_circ_348350,RMVar_hsa_circ_83997,RMVar_hsa_circ_175900,RMVar_hsa_circ_80162,RMVar_hsa_circ_175899,RMVar_hsa_circ_22410,RMVar_hsa_circ_29280,RMVar_hsa_circ_89865,RMVar_hsa_circ_121533,RMVar_hsa_circ_334166,RMVar_hsa_circ_175902,RMVar_hsa_circ_175903,RMVar_hsa_circ_332212,RMVar_hsa_circ_323780,RMVar_hsa_circ_175904,RMVar_hsa_circ_332011,RMVar_hsa_circ_118776,RMVar_hsa_circ_102397,RMVar_hsa_circ_175909,RMVar_hsa_circ_175910,RMVar_hsa_circ_22841,RMVar_hsa_circ_31908,RMVar_hsa_circ_284963,RMVar_hsa_circ_291311,RMVar_hsa_circ_175911,RMVar_hsa_circ_329516,RMVar_hsa_circ_45423 17153 RMVar_ID_17153 Human_SNP_ID_591702051 A-to-I Human chr16 - 3679204 3679204 3679204 CTCACTGCAACCTCTGCCTCCCGGTTCAAGCAACTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGA CTCACTGCAACCTCTGCCTCCCGGTTCAAGCAGCTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGA T C TRAP1 Ensembl:ENSG00000126602 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965131605 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18679105 RMVar_hsa_circ_127986,RMVar_hsa_circ_126602,RMVar_hsa_circ_116781,RMVar_hsa_circ_104500,RMVar_hsa_circ_175884,RMVar_hsa_circ_175882,RMVar_hsa_circ_175883,RMVar_hsa_circ_175881,RMVar_hsa_circ_15167,RMVar_hsa_circ_65550,RMVar_hsa_circ_348350,RMVar_hsa_circ_83997,RMVar_hsa_circ_175900,RMVar_hsa_circ_80162,RMVar_hsa_circ_175899,RMVar_hsa_circ_22410,RMVar_hsa_circ_29280,RMVar_hsa_circ_89865,RMVar_hsa_circ_121533,RMVar_hsa_circ_334166,RMVar_hsa_circ_175902,RMVar_hsa_circ_175903,RMVar_hsa_circ_332212,RMVar_hsa_circ_323780,RMVar_hsa_circ_175904,RMVar_hsa_circ_332011,RMVar_hsa_circ_118776,RMVar_hsa_circ_102397,RMVar_hsa_circ_175909,RMVar_hsa_circ_175910,RMVar_hsa_circ_22841,RMVar_hsa_circ_31908,RMVar_hsa_circ_284963,RMVar_hsa_circ_291311,RMVar_hsa_circ_175911,RMVar_hsa_circ_329516,RMVar_hsa_circ_45423 17154 RMVar_ID_17154 Human_SNP_ID_591702392 A-to-I Human chr16 - 3680139 3680139 3680139 TCTCTGCCTCCTGGGTTCACTGGGCTCAAGCAATTTTCCTGCCTCAGCCTCCGAGTAGCTGGAAC TCTCTGCCTCCTGGGTTCACTGGGCTCAAGCAGTTTTCCTGCCTCAGCCTCCGAGTAGCTGGAAC T C TRAP1 Ensembl:ENSG00000126602 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs549456829 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8433439,Human_RBP_ID_12730520 RMVar_hsa_circ_127986,RMVar_hsa_circ_116781,RMVar_hsa_circ_104500,RMVar_hsa_circ_175882,RMVar_hsa_circ_175883,RMVar_hsa_circ_175881,RMVar_hsa_circ_15167,RMVar_hsa_circ_65550,RMVar_hsa_circ_348350,RMVar_hsa_circ_83997,RMVar_hsa_circ_175900,RMVar_hsa_circ_22410,RMVar_hsa_circ_29280,RMVar_hsa_circ_89865,RMVar_hsa_circ_121533,RMVar_hsa_circ_334166,RMVar_hsa_circ_175902,RMVar_hsa_circ_175903,RMVar_hsa_circ_332212,RMVar_hsa_circ_323780,RMVar_hsa_circ_175904,RMVar_hsa_circ_118776,RMVar_hsa_circ_102397,RMVar_hsa_circ_175909,RMVar_hsa_circ_175910,RMVar_hsa_circ_22841,RMVar_hsa_circ_284963,RMVar_hsa_circ_291311,RMVar_hsa_circ_175911,RMVar_hsa_circ_329516,RMVar_hsa_circ_175913,RMVar_hsa_circ_284192,RMVar_hsa_circ_273546 17155 RMVar_ID_17155 Human_SNP_ID_591703178 A-to-I Human chr16 - 3682665 3682665 3682665 TTTTTTGCCAGGCATGGTGGCTCACGCCTGTAATCCTAGCACTTTGGGAGGCCGTGGCGGGCAGA TTTTTTGCCAGGCATGGTGGCTCACGCCTGTAGTCCTAGCACTTTGGGAGGCCGTGGCGGGCAGA T C TRAP1 Ensembl:ENSG00000126602 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1019822998 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20118544 RMVar_hsa_circ_127986,RMVar_hsa_circ_116781,RMVar_hsa_circ_104500,RMVar_hsa_circ_175882,RMVar_hsa_circ_175883,RMVar_hsa_circ_175881,RMVar_hsa_circ_15167,RMVar_hsa_circ_65550,RMVar_hsa_circ_348350,RMVar_hsa_circ_83997,RMVar_hsa_circ_175900,RMVar_hsa_circ_22410,RMVar_hsa_circ_29280,RMVar_hsa_circ_89865,RMVar_hsa_circ_121533,RMVar_hsa_circ_334166,RMVar_hsa_circ_175902,RMVar_hsa_circ_175903,RMVar_hsa_circ_332212,RMVar_hsa_circ_323780,RMVar_hsa_circ_175904,RMVar_hsa_circ_118776,RMVar_hsa_circ_102397,RMVar_hsa_circ_175909,RMVar_hsa_circ_175910,RMVar_hsa_circ_22841,RMVar_hsa_circ_284963,RMVar_hsa_circ_291311,RMVar_hsa_circ_175911,RMVar_hsa_circ_329516,RMVar_hsa_circ_175913,RMVar_hsa_circ_284192,RMVar_hsa_circ_273546 17156 RMVar_ID_17156 Human_SNP_ID_591709407 A-to-I Human chr16 - 3699894 3699894 3699894 AAGGTAGGAAGATTGCTTGAGACCAGGAGCTTAAGACCAGCCTGGTCAACATGGAAACACCCTAT AAGGTAGGAAGATTGCTTGAGACCAGGAGCTTGAGACCAGCCTGGTCAACATGGAAACACCCTAT T C TRAP1 Ensembl:ENSG00000126602 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs988919071 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25244370 RMVar_hsa_circ_104500,RMVar_hsa_circ_175881,RMVar_hsa_circ_121533,RMVar_hsa_circ_175902,RMVar_hsa_circ_102397,RMVar_hsa_circ_175910,RMVar_hsa_circ_175917,RMVar_hsa_circ_340805 17157 RMVar_ID_17157 Human_SNP_ID_591712458 A-to-I Human chr16 - 3707955 3707955 3707955 GTCTTGAACTCCTGGTCTCAAGTGATCCTCCTACTTCTGCCTGCCAAAGTACTGGGATTACACGC GTCTTGAACTCCTGGTCTCAAGTGATCCTCCTCCTTCTGCCTGCCAAAGTACTGGGATTACACGC T G TRAP1 Ensembl:ENSG00000126602 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917160633 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104500,RMVar_hsa_circ_175881,RMVar_hsa_circ_121533,RMVar_hsa_circ_175902,RMVar_hsa_circ_102397,RMVar_hsa_circ_175910,RMVar_hsa_circ_175917,RMVar_hsa_circ_340805 17158 RMVar_ID_17158 Human_SNP_ID_591727116 A-to-I Human chr16 - 3750003 3750003 3750003 CATGCCTATAGTCCCAGCTACCCAGGAGGATCACTTGAGCCTAGGAGGTTAAGGCTGCAGTGAGC CATGCCTATAGTCCCAGCTACCCAGGAGGATCGCTTGAGCCTAGGAGGTTAAGGCTGCAGTGAGC T C CREBBP Ensembl:ENSG00000005339 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1172993622 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50096,RMVar_hsa_circ_268634,RMVar_hsa_circ_265959,RMVar_hsa_circ_125258,RMVar_hsa_circ_10415,RMVar_hsa_circ_175919,RMVar_hsa_circ_175927,RMVar_hsa_circ_21809,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_45466,RMVar_hsa_circ_307611,RMVar_hsa_circ_338177,RMVar_hsa_circ_282138,RMVar_hsa_circ_175928,RMVar_hsa_circ_175926 17159 RMVar_ID_17159 Human_SNP_ID_591732521 A-to-I Human chr16 - 3767860 3767860 3767860 GCAAGGAGCTTCCCAAGTTAAAGAAGAAACAGACATAGCAGAGCAGAAATCAGAACCAATGGAAG GCAAGGAGCTTCCCAAGTTAAAGAAGAAACAGGCATAGCAGAGCAGAAATCAGAACCAATGGAAG T C CREBBP Ensembl:ENSG00000005339 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs755638291 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_895807,Human_RBP_ID_1842374,Human_RBP_ID_6512017,Human_RBP_ID_8807735,Human_RBP_ID_9372171,Human_RBP_ID_17486412,Human_RBP_ID_26329734 Human_Splice_Rec_1670756,Human_Splice_Rec_1670814,Human_Splice_Rec_1670878,Human_Splice_Rec_1670930 Human_miRNA_ID_2395831,Human_miRNA_ID_2908179,Human_miRNA_ID_2979647,Human_miRNA_ID_3027018 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 17160 RMVar_ID_17160 Human_SNP_ID_591736428 A-to-I Human chr16 - 3779463 3779463 3779463 GATGGCATTGGAAGTAGCTTCAGGCCAGGTGCAGTGGCCCCCACGTGTAATTCCAGTGCTTTGGG GATGGCATTGGAAGTAGCTTCAGGCCAGGTGCTGTGGCCCCCACGTGTAATTCCAGTGCTTTGGG T A CREBBP Ensembl:ENSG00000005339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1003351141 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6512101,Human_RBP_ID_12732666 RMVar_hsa_circ_265959,RMVar_hsa_circ_125258,RMVar_hsa_circ_175919,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_43645,RMVar_hsa_circ_371775,RMVar_hsa_circ_175938,RMVar_hsa_circ_374397,RMVar_hsa_circ_84211,RMVar_hsa_circ_175943,RMVar_hsa_circ_56854,RMVar_hsa_circ_175944,RMVar_hsa_circ_175942,RMVar_hsa_circ_121414,RMVar_hsa_circ_78351,RMVar_hsa_circ_121376,RMVar_hsa_circ_175946,RMVar_hsa_circ_175945,RMVar_hsa_circ_175949,RMVar_hsa_circ_74810 17161 RMVar_ID_17161 Human_SNP_ID_591761821 A-to-I Human chr16 - 3862785 3862785 3862785 GCAGGGACGGAAGACAGCAAGGCAGGCAGGCAAAGCTGGCTGCTCTGCCGTGGGGAGCTTCAAGG GCAGGGACGGAAGACAGCAAGGCAGGCAGGCAGAGCTGGCTGCTCTGCCGTGGGGAGCTTCAAGG T C CREBBP Ensembl:ENSG00000005339 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs547259291 Functional Loss SNV dbSNP153 33..33 33 - - - 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 17162 RMVar_ID_17162 Human_SNP_ID_591761847 A-to-I Human chr16 - 3862880 3862880 3862880 GAATATTTGTCCTGTAATTTAGCTTTCAAATAAGAGGCAAACTCTGAGCAGAACTTCAGAGGGAA GAATATTTGTCCTGTAATTTAGCTTTCAAATATGAGGCAAACTCTGAGCAGAACTTCAGAGGGAA T A CREBBP Ensembl:ENSG00000005339 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054632455 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18513011 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 17163 RMVar_ID_17163 Human_SNP_ID_591816971 A-to-I Human chr16 - 4039992 4039992 4039992 CTCTGCCACCCAGCCTGGAGTGCAGTGGTGCAATCATGGGTCACCGCAGCCCCTACCTCCTGGGC CTCTGCCACCCAGCCTGGAGTGCAGTGGTGCAGTCATGGGTCACCGCAGCCCCTACCTCCTGGGC T C ADCY9 Ensembl:ENSG00000162104 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs530767626 Functional Loss SNV dbSNP153 33..33 33 - - - 17164 RMVar_ID_17164 Human_SNP_ID_591817563 A-to-I Human chr16 - 4041859 4041856 4041859 AGGTCCCAGCTACTTGGGAGGCCGAGGTGGGAAGATGGCTTGGGCCCAGGTGATCGAGGCTTTAG AGGTCCCAGCTACTTGGGAGGCCGAGGTGGGA___TGGCTTGGGCCCAGGTGATCGAGGCTTTAG ATCT A ADCY9 Ensembl:ENSG00000162104 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1240545312 Functional Loss DEL dbSNP153 33..35 33 - - - 17165 RMVar_ID_17165 Human_SNP_ID_591817564 A-to-I Human chr16 - 4041859 4041859 4041859 AGGTCCCAGCTACTTGGGAGGCCGAGGTGGGAAGATGGCTTGGGCCCAGGTGATCGAGGCTTTAG AGGTCCCAGCTACTTGGGAGGCCGAGGTGGGAGGATGGCTTGGGCCCAGGTGATCGAGGCTTTAG T C ADCY9 Ensembl:ENSG00000162104 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs980600747 Functional Loss SNV dbSNP153 33..33 33 - - - 17166 RMVar_ID_17166 Human_SNP_ID_591817565 A-to-I Human chr16 - 4041859 4041859 4041859 AGGTCCCAGCTACTTGGGAGGCCGAGGTGGGAAGATGGCTTGGGCCCAGGTGATCGAGGCTTTAG AGGTCCCAGCTACTTGGGAGGCCGAGGTGGGACGATGGCTTGGGCCCAGGTGATCGAGGCTTTAG T G ADCY9 Ensembl:ENSG00000162104 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs980600747 Functional Loss SNV dbSNP153 33..33 33 - - - 17167 RMVar_ID_17167 Human_SNP_ID_591838009 A-to-I Human chr16 - 4108485 4108485 4108485 CCTTTAGTCCCAGCCACTTGGGAAGCTGAGGCAGGAGAATCGTTCGAACCCAGGAGGTGGAGTTT CCTTTAGTCCCAGCCACTTGGGAAGCTGAGGCGGGAGAATCGTTCGAACCCAGGAGGTGGAGTTT T C ADCY9 Ensembl:ENSG00000162104 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1039720195 Functional Loss SNV dbSNP153 33..33 33 - - - 17168 RMVar_ID_17168 Human_SNP_ID_591882827 A-to-I Human chr16 - 4250428 4250428 4250428 TTTTGTATTGTTAGTACAGACAGGATTTTGCCATGTTGGCCAGGCTGGTCTCCAACCCCTGGCCT TTTTGTATTGTTAGTACAGACAGGATTTTGCCGTGTTGGCCAGGCTGGTCTCCAACCCCTGGCCT T C LINC01569 Ensembl:ENSG00000262468 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1033174860 Functional Loss SNV dbSNP153 33..33 33 - - - 17169 RMVar_ID_17169 Human_SNP_ID_591882828 A-to-I Human chr16 - 4250428 4250428 4250428 TTTTGTATTGTTAGTACAGACAGGATTTTGCCATGTTGGCCAGGCTGGTCTCCAACCCCTGGCCT TTTTGTATTGTTAGTACAGACAGGATTTTGCCCTGTTGGCCAGGCTGGTCTCCAACCCCTGGCCT T G LINC01569 Ensembl:ENSG00000262468 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1033174860 Functional Loss SNV dbSNP153 33..33 33 - - - 17170 RMVar_ID_17170 Human_SNP_ID_591885629 A-to-I Human chr16 - 4259041 4259041 4259041 TCTTATTGCCCAGGCTGGAGTGCAATGGTGCTATCTCAGCTCATCGCAACCTCCTCCTCCCAGGT TCTTATTGCCCAGGCTGGAGTGCAATGGTGCTGTCTCAGCTCATCGCAACCTCCTCCTCCCAGGT T C TFAP4 Ensembl:ENSG00000090447 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs969605127 Functional Loss SNV dbSNP153 33..33 33 - - - 17171 RMVar_ID_17171 Human_SNP_ID_591887518 A-to-I Human chr16 - 4265489 4265487 4265490 CCTCCCACCTTAGCCTCCTCAGTTGCTGGAACAATAGGGACACTCCACCATGCCTGGCTGATTAA CCTCCCACCTTAGCCTCCTCAGTTGCTGGAA___TAGGGACACTCCACCATGCCTGGCTGATTAA ATTG A TFAP4 Ensembl:ENSG00000090447 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1249004720 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_12736034 RMVar_hsa_circ_2265 17172 RMVar_ID_17172 Human_SNP_ID_591888322 A-to-I Human chr16 - 4268264 4268264 4268264 CACGACACCCGGCTAATTTTTGTATTTTTAGTAGAGAGGGGGTTTCACCATCTTGGCCTGGCTGG CACGACACCCGGCTAATTTTTGTATTTTTAGTGGAGAGGGGGTTTCACCATCTTGGCCTGGCTGG T C TFAP4 Ensembl:ENSG00000090447 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1429312267 Functional Loss SNV dbSNP153 33..33 33 - - - 17173 RMVar_ID_17173 Human_SNP_ID_591888783 A-to-I Human chr16 - 4269723 4269723 4269723 TCACTGCAACTTCTGCCTCCGGGGTTCAAGCAATTTTCCTGCCTCAGCCTCCTAAGTAACTGGGA TCACTGCAACTTCTGCCTCCGGGGTTCAAGCAGTTTTCCTGCCTCAGCCTCCTAAGTAACTGGGA T C TFAP4 Ensembl:ENSG00000090447 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs555325656 Functional Loss SNV dbSNP153 33..33 33 - - - 17174 RMVar_ID_17174 Human_SNP_ID_591894077 A-to-I Human chr16 - 4286613 4286613 4286613 TTGCCCAGGCTGATCTCGAACTCTTGACCTCAAGTGATCCGCCCGCCCCTACCTACCAAAGTGTT TTGCCCAGGCTGATCTCGAACTCTTGACCTCAGGTGATCCGCCCGCCCCTACCTACCAAAGTGTT 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 GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1029600643 Functional Loss SNV dbSNP153 33..33 33 - - - 17175 RMVar_ID_17175 Human_SNP_ID_591898193 A-to-I Human chr16 - 4299723 4299723 4299723 GTGGTCTCCATCTCCTGACCTCATGATCTGCCAGCCTTAGCCTCCCAAAGTGCTGGGATTACAGG GTGGTCTCCATCTCCTGACCTCATGATCTGCCCGCCTTAGCCTCCCAAAGTGCTGGGATTACAGG T G 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 intron,exon,exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1458382924 Functional Loss SNV dbSNP153 33..33 33 - - - 17176 RMVar_ID_17176 Human_SNP_ID_591898494 A-to-I Human chr16 - 4300573 4300573 4300573 CCTCAGCCTCAGCCTCCCGAGTCGCTGGGACTACAGGTGCCTGCCACAATGTCTGGCTAATTTTT CCTCAGCCTCAGCCTCCCGAGTCGCTGGGACTGCAGGTGCCTGCCACAATGTCTGGCTAATTTTT 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 GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs565753171 Functional Loss SNV dbSNP153 33..33 33 - - - 17177 RMVar_ID_17177 Human_SNP_ID_591899200 A-to-I Human chr16 - 4302888 4302888 4302888 TCAAGCGATTCTCCTGCCTCAGCCTCCGGAGTAGCTGGACTACAGGTGCCTGCCACCACGCCCGG TCAAGCGATTCTCCTGCCTCAGCCTCCGGAGTGGCTGGACTACAGGTGCCTGCCACCACGCCCGG 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 GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs776488946 Functional Loss SNV dbSNP153 33..33 33 - - - 17178 RMVar_ID_17178 Human_SNP_ID_591899825 A-to-I Human chr16 - 4304896 4304896 4304896 TTTCACTCTTTGTTTGCCCAGTCTGGAATGCAATGGCACAATCTCAGCTCACTGCAACCTCTGCC TTTCACTCTTTGTTTGCCCAGTCTGGAATGCAGTGGCACAATCTCAGCTCACTGCAACCTCTGCC T C lnc-TFAP4-3,lnc-TFAP4-3:2,lnc-TFAP4-3:3,lnc-TFAP4-3:4,lnc-TFAP4-3:5 RNACentral:URS0000D574AE,RNACentral:URS0000D5E22E,RNACentral:URS00008BBD57,RNACentral:URS0000D5DCB2,RNACentral:URS0000D5D47B lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs867515313 Functional Loss SNV dbSNP153 33..33 33 - - - 17179 RMVar_ID_17179 Human_SNP_ID_591899944 A-to-I Human chr16 - 4305266 4305266 4305266 AACCCTGTCTCTACTAAAAATACAAAAAAATTAGCTGAACGTGGTGGCGGGCGCCTGTAGCCCCA AACCCTGTCTCTACTAAAAATACAAAAAAATTTGCTGAACGTGGTGGCGGGCGCCTGTAGCCCCA T A lnc-TFAP4-3,lnc-TFAP4-3:2,lnc-TFAP4-3:3,lnc-TFAP4-3:4,lnc-TFAP4-3:5 RNACentral:URS0000D574AE,RNACentral:URS0000D5E22E,RNACentral:URS00008BBD57,RNACentral:URS0000D5DCB2,RNACentral:URS0000D5D47B lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1206949401 Functional Loss SNV dbSNP153 33..33 33 - - - 17180 RMVar_ID_17180 Human_SNP_ID_591900191 A-to-I Human chr16 - 4305982 4305982 4305982 TCTATTAGCGGGGCGTGATGGCACATGGCTGTAGTCCCAGCTACTCTGGAGGCTGAAGCAAGAGA TCTATTAGCGGGGCGTGATGGCACATGGCTGTCGTCCCAGCTACTCTGGAGGCTGAAGCAAGAGA T G lnc-TFAP4-3,lnc-TFAP4-3:2,lnc-TFAP4-3:3,lnc-TFAP4-3:4,lnc-TFAP4-3:5,lnc-TFAP4-3:6 RNACentral:URS0000D574AE,RNACentral:URS0000D57CA6,RNACentral:URS0000D5E22E,RNACentral:URS00008BBD57,RNACentral:URS0000D5DCB2,RNACentral:URS0000D5D47B lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,exon,exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs750035273 Functional Loss SNV dbSNP153 33..33 33 - - - 17181 RMVar_ID_17181 Human_SNP_ID_591908061 A-to-I Human chr16 + 4331187 4331187 4331187 GTTATTTAATAGAGTTGGGGTTTCAGCGTGTTAGCCAGGATGGTCTCTATCTCCTGACCTCGTGA GTTATTTAATAGAGTTGGGGTTTCAGCGTGTTGGCCAGGATGGTCTCTATCTCCTGACCTCGTGA A G GLIS2 Ensembl:ENSG00000126603 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs369535403 Functional Loss SNV dbSNP153 33..33 33 - - - 17182 RMVar_ID_17182 Human_SNP_ID_591913863 A-to-I Human chr16 - 4347426 4347425 4347426 AGTTAAGAAAACTGAGGTAGGCTGGGCACAGTAGCTCACACCTGTAATCCTAGCACTTTGGGAAG AGTTAAGAAAACTGAGGTAGGCTGGGCACAGT_GCTCACACCTGTAATCCTAGCACTTTGGGAAG CT C AC012676.5,PAM16,CORO7-PAM16 Ensembl:ENSG00000280063,Ensembl:ENSG00000217930,Ensembl:ENSG00000103426 Other,Protein coding,Protein coding exon,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs544815099 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5097601,Human_RBP_ID_6513024,Human_RBP_ID_12736341,Human_RBP_ID_22581897,Human_RBP_ID_26945070 Clinvar_Rec_64 RMVar_hsa_circ_77031,RMVar_hsa_circ_123394,RMVar_hsa_circ_119552,RMVar_hsa_circ_175984,RMVar_hsa_circ_175985,RMVar_hsa_circ_175983 17183 RMVar_ID_17183 Human_SNP_ID_591913864 A-to-I Human chr16 - 4347426 4347426 4347426 AGTTAAGAAAACTGAGGTAGGCTGGGCACAGTAGCTCACACCTGTAATCCTAGCACTTTGGGAAG AGTTAAGAAAACTGAGGTAGGCTGGGCACAGTGGCTCACACCTGTAATCCTAGCACTTTGGGAAG T C AC012676.5,PAM16,CORO7-PAM16 Ensembl:ENSG00000280063,Ensembl:ENSG00000217930,Ensembl:ENSG00000103426 Other,Protein coding,Protein coding exon,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1018055086 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5097601,Human_RBP_ID_6513024,Human_RBP_ID_12736341,Human_RBP_ID_22581897,Human_RBP_ID_26945070 RMVar_hsa_circ_77031,RMVar_hsa_circ_123394,RMVar_hsa_circ_119552,RMVar_hsa_circ_175984,RMVar_hsa_circ_175985,RMVar_hsa_circ_175983 17184 RMVar_ID_17184 Human_SNP_ID_591914370 A-to-I Human chr16 - 4348935 4348935 4348935 AAAAAAAAAAAAAAGAAAGTGCTAGGCCGGGTACGGTGGCTCACGCCTGTAATCCCAGCACTTTG AAAAAAAAAAAAAAGAAAGTGCTAGGCCGGGTCCGGTGGCTCACGCCTGTAATCCCAGCACTTTG T G PAM16,CORO7-PAM16 Ensembl:ENSG00000217930,Ensembl:ENSG00000103426 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1364962749 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 17185 RMVar_ID_17185 Human_SNP_ID_591914374 A-to-I Human chr16 - 4348944 4348943 4348944 TCTCAAAAAAAAAAAAAAAAAAAGAAAGTGCTAGGCCGGGTACGGTGGCTCACGCCTGTAATCCC TCTCAAAAAAAAAAAAAAAAAAAGAAAGTGCT_GGCCGGGTACGGTGGCTCACGCCTGTAATCCC CT C PAM16,CORO7-PAM16 Ensembl:ENSG00000217930,Ensembl:ENSG00000103426 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1230122129 Functional Loss DEL 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 17186 RMVar_ID_17186 Human_SNP_ID_591914375 A-to-I Human chr16 - 4348944 4348944 4348944 TCTCAAAAAAAAAAAAAAAAAAAGAAAGTGCTAGGCCGGGTACGGTGGCTCACGCCTGTAATCCC TCTCAAAAAAAAAAAAAAAAAAAGAAAGTGCTGGGCCGGGTACGGTGGCTCACGCCTGTAATCCC T C PAM16,CORO7-PAM16 Ensembl:ENSG00000217930,Ensembl:ENSG00000103426 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1290777997 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 17187 RMVar_ID_17187 Human_SNP_ID_591914560 A-to-I Human chr16 - 4349384 4349384 4349384 TTTTGTATTTTTTGTAGAGATGCAGTTTCGCCATGTTGCCAGGCTGGTCTCAAACTTCTGGGCCC TTTTGTATTTTTTGTAGAGATGCAGTTTCGCCGTGTTGCCAGGCTGGTCTCAAACTTCTGGGCCC T C PAM16,CORO7-PAM16 Ensembl:ENSG00000217930,Ensembl:ENSG00000103426 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1174221092 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12736392 RMVar_hsa_circ_77031,RMVar_hsa_circ_123394,RMVar_hsa_circ_119552,RMVar_hsa_circ_175984,RMVar_hsa_circ_175985,RMVar_hsa_circ_175983 17188 RMVar_ID_17188 Human_SNP_ID_591914570 A-to-I Human chr16 - 4349424 4349424 4349424 AGTTGGGACAACAGGCATGCTCCACTATGCCCAGCTAATTTTTTGTATTTTTTGTAGAGATGCAG AGTTGGGACAACAGGCATGCTCCACTATGCCCGGCTAATTTTTTGTATTTTTTGTAGAGATGCAG T C PAM16,CORO7-PAM16 Ensembl:ENSG00000217930,Ensembl:ENSG00000103426 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1453061907 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 17189 RMVar_ID_17189 Human_SNP_ID_591914603 A-to-I Human chr16 - 4349525 4349525 4349525 TGGAGTACAGTGGTACGATCACAGCTCACTGCAGCCTCAACCTCCTGGGGCTTAGGTGATCCTCC TGGAGTACAGTGGTACGATCACAGCTCACTGCGGCCTCAACCTCCTGGGGCTTAGGTGATCCTCC T C PAM16,CORO7-PAM16 Ensembl:ENSG00000217930,Ensembl:ENSG00000103426 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1293979048 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25209898 RMVar_hsa_circ_77031,RMVar_hsa_circ_123394,RMVar_hsa_circ_119552,RMVar_hsa_circ_175984,RMVar_hsa_circ_175985,RMVar_hsa_circ_175983 17190 RMVar_ID_17190 Human_SNP_ID_591914610 A-to-I Human chr16 - 4349551 4349551 4349551 TGTTGCCCCAGATGGGTCTCCTAGGCTGGAGTACAGTGGTACGATCACAGCTCACTGCAGCCTCA TGTTGCCCCAGATGGGTCTCCTAGGCTGGAGTTCAGTGGTACGATCACAGCTCACTGCAGCCTCA T A PAM16,CORO7-PAM16 Ensembl:ENSG00000217930,Ensembl:ENSG00000103426 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs146765584 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22473764 RMVar_hsa_circ_77031,RMVar_hsa_circ_123394,RMVar_hsa_circ_119552,RMVar_hsa_circ_175984,RMVar_hsa_circ_175985,RMVar_hsa_circ_175983 17191 RMVar_ID_17191 Human_SNP_ID_591914629 A-to-I Human chr16 - 4349619 4349619 4349619 GGGCCTACAGGTGAGTGCCAGCACACCTGGCTAATTTTTAAATTTTATGTAGAGGTGGGGTCTTG GGGCCTACAGGTGAGTGCCAGCACACCTGGCTCATTTTTAAATTTTATGTAGAGGTGGGGTCTTG T G PAM16,CORO7-PAM16 Ensembl:ENSG00000217930,Ensembl:ENSG00000103426 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1198031575 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9826277 RMVar_hsa_circ_77031,RMVar_hsa_circ_123394,RMVar_hsa_circ_119552,RMVar_hsa_circ_175984,RMVar_hsa_circ_175985,RMVar_hsa_circ_175983 17192 RMVar_ID_17192 Human_SNP_ID_591914642 A-to-I Human chr16 - 4349672 4349672 4349672 GCCTTGAACTCCTAGGCTCAAGCCATCCTCCTACCTTAGACCCCCAAGTAGTTGGGCCTACAGGT GCCTTGAACTCCTAGGCTCAAGCCATCCTCCTTCCTTAGACCCCCAAGTAGTTGGGCCTACAGGT T A PAM16,CORO7-PAM16 Ensembl:ENSG00000217930,Ensembl:ENSG00000103426 Protein coding,Protein coding intron,intron GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs931586012 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 17193 RMVar_ID_17193 Human_SNP_ID_591914660 A-to-I Human chr16 - 4349715 4349715 4349715 TCGCCCCGGCTAGGATGCAGTGGAGCGATCCTAGCTCACTGCAGCCTTGAACTCCTAGGCTCAAG TCGCCCCGGCTAGGATGCAGTGGAGCGATCCTGGCTCACTGCAGCCTTGAACTCCTAGGCTCAAG T C PAM16,CORO7-PAM16 Ensembl:ENSG00000217930,Ensembl:ENSG00000103426 Protein coding,Protein coding intron,intron GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,29796672,31158229,32596459 RNA-Seq:(High) rs1567234012 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 17194 RMVar_ID_17194 Human_SNP_ID_591914665 A-to-I Human chr16 - 4349729 4349729 4349729 AGGATGTCTGTCTGTCGCCCCGGCTAGGATGCAGTGGAGCGATCCTAGCTCACTGCAGCCTTGAA AGGATGTCTGTCTGTCGCCCCGGCTAGGATGCGGTGGAGCGATCCTAGCTCACTGCAGCCTTGAA T C PAM16,CORO7-PAM16 Ensembl:ENSG00000217930,Ensembl:ENSG00000103426 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1029263451 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5128485,Human_RBP_ID_22474352 RMVar_hsa_circ_77031,RMVar_hsa_circ_123394,RMVar_hsa_circ_119552,RMVar_hsa_circ_175984,RMVar_hsa_circ_175985,RMVar_hsa_circ_175983 17195 RMVar_ID_17195 Human_SNP_ID_591915010 A-to-I Human chr16 - 4350573 4350573 4350573 CATGATGAAACCCGGTCTCCACCAAAAAATTTAAAAAATTAGCCGGGTGGGGTGGTGCGCGCCTG CATGATGAAACCCGGTCTCCACCAAAAAATTTTAAAAATTAGCCGGGTGGGGTGGTGCGCGCCTG T A PAM16,CORO7-PAM16 Ensembl:ENSG00000217930,Ensembl:ENSG00000103426 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs950138641 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 17196 RMVar_ID_17196 Human_SNP_ID_591915013 A-to-I Human chr16 - 4350579 4350579 4350579 GGCCAACATGATGAAACCCGGTCTCCACCAAAAAATTTAAAAAATTAGCCGGGTGGGGTGGTGCG GGCCAACATGATGAAACCCGGTCTCCACCAAAGAATTTAAAAAATTAGCCGGGTGGGGTGGTGCG T C PAM16,CORO7-PAM16 Ensembl:ENSG00000217930,Ensembl:ENSG00000103426 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1440143503 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 17197 RMVar_ID_17197 Human_SNP_ID_591939708 A-to-I Human chr16 - 4425133 4425133 4425133 TTTAGTAGAGACGGGGTTTCACCATCTTGGCCAGGCTGGGTCTTGAACTCCTGACCTCGTGATCC TTTAGTAGAGACGGGGTTTCACCATCTTGGCCCGGCTGGGTCTTGAACTCCTGACCTCGTGATCC T G CORO7 Ensembl:ENSG00000262246 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909301702 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12736571 17198 RMVar_ID_17198 Human_SNP_ID_591941261 A-to-I Human chr16 + 4429070 4429070 4429070 GCAACCGCGCCCAGCTAATTTTTTGTATTTTTAGTAGAGATGGAGTTTCACTGTGTTAGCCAGGA GCAACCGCGCCCAGCTAATTTTTTGTATTTTTGGTAGAGATGGAGTTTCACTGTGTTAGCCAGGA A G DNAJA3 Ensembl:ENSG00000103423 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs932298353 Functional Loss SNV dbSNP153 33..33 33 - - - 17199 RMVar_ID_17199 Human_SNP_ID_591941404 A-to-I Human chr16 + 4429426 4429426 4429426 TTGTATTTTTAGCAGATACTGGATTTCACCATATTGGCCAGGATGGTCTCGATCTCTTTACCCAT TTGTATTTTTAGCAGATACTGGATTTCACCATGTTGGCCAGGATGGTCTCGATCTCTTTACCCAT A G DNAJA3 Ensembl:ENSG00000103423 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs530333932 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12736698 17200 RMVar_ID_17200 Human_SNP_ID_591941498 A-to-I Human chr16 + 4429679 4429679 4429679 CAACATGGAGAAACCCCGTCTCTACAAAAAATACAAAATTAGCCAGGCCTGGTGGCGCATGCCTG CAACATGGAGAAACCCCGTCTCTACAAAAAATGCAAAATTAGCCAGGCCTGGTGGCGCATGCCTG A G DNAJA3 Ensembl:ENSG00000103423 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1042689302 Functional Loss SNV dbSNP153 33..33 33 - - - 17201 RMVar_ID_17201 Human_SNP_ID_591941659 A-to-I Human chr16 + 4430118 4430118 4430118 ATTGCTGGAGTCCAGGAATTTGAATTTGGCCTAGGCAACATAATGAGACCCCTGTCTCTTAAAAA ATTGCTGGAGTCCAGGAATTTGAATTTGGCCTGGGCAACATAATGAGACCCCTGTCTCTTAAAAA A G DNAJA3 Ensembl:ENSG00000103423 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1344440191 Functional Loss SNV dbSNP153 33..33 33 - - - 17202 RMVar_ID_17202 Human_SNP_ID_591941730 A-to-I Human chr16 + 4430352 4430352 4430352 TACTTTGGGAGGTGGGTTGATCGCCTGAGGTCAGGAGTTTGAGACCAGCCTGGCCAAGATGGCCA TACTTTGGGAGGTGGGTTGATCGCCTGAGGTCCGGAGTTTGAGACCAGCCTGGCCAAGATGGCCA A C DNAJA3 Ensembl:ENSG00000103423 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1374086496 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25209988 17203 RMVar_ID_17203 Human_SNP_ID_591941731 A-to-I Human chr16 + 4430352 4430352 4430352 TACTTTGGGAGGTGGGTTGATCGCCTGAGGTCAGGAGTTTGAGACCAGCCTGGCCAAGATGGCCA TACTTTGGGAGGTGGGTTGATCGCCTGAGGTCGGGAGTTTGAGACCAGCCTGGCCAAGATGGCCA A G DNAJA3 Ensembl:ENSG00000103423 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1374086496 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25209988 17204 RMVar_ID_17204 Human_SNP_ID_591941913 A-to-I Human chr16 + 4430921 4430921 4430921 CAAAAATTAGCCAGGTGTGGTGGTGTGCGCCTATAGTCCTGGCTACTTGAGAGGCTAAAGCAGAA CAAAAATTAGCCAGGTGTGGTGGTGTGCGCCTGTAGTCCTGGCTACTTGAGAGGCTAAAGCAGAA A G AC012676.4,DNAJA3 Ensembl:ENSG00000277440,Ensembl:ENSG00000103423 lincRNA,Protein coding exon,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1233774565 Functional Loss SNV dbSNP153 33..33 33 - - - 17205 RMVar_ID_17205 Human_SNP_ID_591944574 A-to-I Human chr16 + 4438729 4438729 4438729 GAACTCCTGAGCTGAAGAGATCCTCCTGCCTCAGCCTCTCAAATTGCTAGGATTATAGGTGCAAG GAACTCCTGAGCTGAAGAGATCCTCCTGCCTCGGCCTCTCAAATTGCTAGGATTATAGGTGCAAG A G DNAJA3 Ensembl:ENSG00000103423 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1024833475 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_175999,RMVar_hsa_circ_369834,RMVar_hsa_circ_376232,RMVar_hsa_circ_175998 17206 RMVar_ID_17206 Human_SNP_ID_591944771 A-to-I Human chr16 + 4439385 4439385 4439385 ATCAAAAAAAAAAAAAAAAGAGTTGAGGTCTCACTCTGTTACCTAGGCTGGAGTGTAGTGGCGAG ATCAAAAAAAAAAAAAAAAGAGTTGAGGTCTCGCTCTGTTACCTAGGCTGGAGTGTAGTGGCGAG A G DNAJA3 Ensembl:ENSG00000103423 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1341698167 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_175999,RMVar_hsa_circ_369834,RMVar_hsa_circ_376232,RMVar_hsa_circ_175998 17207 RMVar_ID_17207 Human_SNP_ID_591944975 A-to-I Human chr16 + 4440182 4440182 4440182 GCTGGTCTTGAACTCATGAACTCAAGCAGTCCACCTGCCTTGGCCTCCCAAAGTCCTGGGATTAC GCTGGTCTTGAACTCATGAACTCAAGCAGTCCCCCTGCCTTGGCCTCCCAAAGTCCTGGGATTAC A C DNAJA3 Ensembl:ENSG00000103423 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs923398099 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12737037 RMVar_hsa_circ_175999,RMVar_hsa_circ_369834,RMVar_hsa_circ_376232,RMVar_hsa_circ_175998 17208 RMVar_ID_17208 Human_SNP_ID_591945176 A-to-I Human chr16 + 4440906 4440906 4440906 AGGCAGGAGGATTGCTTCAACCTGGGAGGTTGAGGCTGCAGTGAGCTAGGATTGCACCACTGCTA AGGCAGGAGGATTGCTTCAACCTGGGAGGTTGGGGCTGCAGTGAGCTAGGATTGCACCACTGCTA A G DNAJA3 Ensembl:ENSG00000103423 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1028756355 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_474100,Human_RBP_ID_12737049 RMVar_hsa_circ_175999,RMVar_hsa_circ_369834,RMVar_hsa_circ_376232,RMVar_hsa_circ_175998 17209 RMVar_ID_17209 Human_SNP_ID_591949208 A-to-I Human chr16 + 4453124 4453124 4453124 TGGCCCAGCCTGGAGTGCAGTGGTGCAGTCATAGCTCACGGCAGCCTCAAACTCCTGGACTCAAG TGGCCCAGCCTGGAGTGCAGTGGTGCAGTCATGGCTCACGGCAGCCTCAAACTCCTGGACTCAAG A G DNAJA3 Ensembl:ENSG00000103423 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs997118543 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_176006,RMVar_hsa_circ_378017 17210 RMVar_ID_17210 Human_SNP_ID_591950814 A-to-I Human chr16 - 4458857 4458857 4458857 GGATTACAGGCGCCCACCACCAAGTCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCAC GGATTACAGGCGCCCACCACCAAGTCTGGCTAGTTTTTGTATTTTTAGTAGAGACAGGGTTTCAC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048971705 Functional Loss SNV dbSNP153 33..33 33 - - - 17211 RMVar_ID_17211 Human_SNP_ID_591950837 A-to-I Human chr16 - 4458924 4458924 4458924 CTGGCTCACTGCAACCTCCACCTCCAGGGTTCAAGCGGATCTCCTGCCTCAGCCTGCCGAGTAGC CTGGCTCACTGCAACCTCCACCTCCAGGGTTCCAGCGGATCTCCTGCCTCAGCCTGCCGAGTAGC T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956719308 Functional Loss SNV dbSNP153 33..33 33 - - - 17212 RMVar_ID_17212 Human_SNP_ID_591951027 A-to-I Human chr16 - 4459668 4459668 4459668 CCTGTACTCCCAGCTACTCAGGAAGCTGTGGTAGGAGGATCACTTGAGCCCAGGAGGTCAAGGCT CCTGTACTCCCAGCTACTCAGGAAGCTGTGGTGGGAGGATCACTTGAGCCCAGGAGGTCAAGGCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs551285952 Functional Loss SNV dbSNP153 33..33 33 - - - 17213 RMVar_ID_17213 Human_SNP_ID_591951071 A-to-I Human chr16 - 4459853 4459853 4459853 CTGGGCGTGGTGGCGTGTGCCGGCAGCTACTCAGGAGGCTGAGGCAGGAGAATCAGCTGAACCCA CTGGGCGTGGTGGCGTGTGCCGGCAGCTACTCGGGAGGCTGAGGCAGGAGAATCAGCTGAACCCA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1343114811 Functional Loss SNV dbSNP153 33..33 33 - - - 17214 RMVar_ID_17214 Human_SNP_ID_591951991 A-to-I Human chr16 - 4462396 4462396 4462396 TCAGCTCACTGCAACCTCCACCTCCTGGTTTCAAGCGATTCTCCTGTCTCAGCCTCCTAAGTAGC TCAGCTCACTGCAACCTCCACCTCCTGGTTTCGAGCGATTCTCCTGTCTCAGCCTCCTAAGTAGC T C NMRAL1 Ensembl:ENSG00000153406 Protein coding intron GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs1297772308 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104600,RMVar_hsa_circ_108642,RMVar_hsa_circ_176009,RMVar_hsa_circ_176010 17215 RMVar_ID_17215 Human_SNP_ID_591951996 A-to-I Human chr16 - 4462426 4462426 4462426 TTGCCCAGGCTGGAGTACAGTGGGGTGATCTCAGCTCACTGCAACCTCCACCTCCTGGTTTCAAG TTGCCCAGGCTGGAGTACAGTGGGGTGATCTCGGCTCACTGCAACCTCCACCTCCTGGTTTCAAG T C NMRAL1 Ensembl:ENSG00000153406 Protein coding intron GSE38233;GSE99789 cultured B-cells;esophageal squamous carcinoma cells,EC109 - 24183664,29796672 RNA-Seq:(High) rs1357302641 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104600,RMVar_hsa_circ_108642,RMVar_hsa_circ_176009,RMVar_hsa_circ_176010 17216 RMVar_ID_17216 Human_SNP_ID_591952152 A-to-I Human chr16 - 4462965 4462965 4462965 CTGTAATCCCAGCTACTTGGGAGGCTGAGGCAAGAGAATCGCTTGAACTCAGGAGGCAGAGTTTG CTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAACTCAGGAGGCAGAGTTTG T C NMRAL1 Ensembl:ENSG00000153406 Protein coding intron GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs545975999 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104600,RMVar_hsa_circ_108642,RMVar_hsa_circ_176009,RMVar_hsa_circ_176010 17217 RMVar_ID_17217 Human_SNP_ID_591952201 A-to-I Human chr16 - 4463122 4463122 4463122 GGCTGGGTGCAGTAGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGTGGATCACC GGCTGGGTGCAGTAGCTCACGCCTGTAATCCCTGCACTTTGGGAGGCCGAGGCAGGTGGATCACC T A NMRAL1 Ensembl:ENSG00000153406 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1394969108 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104600,RMVar_hsa_circ_108642,RMVar_hsa_circ_176009,RMVar_hsa_circ_176010 17218 RMVar_ID_17218 Human_SNP_ID_591952209 A-to-I Human chr16 - 4463141 4463141 4463141 CTCATTAAAGAATCTGGGAGGCTGGGTGCAGTAGCTCACGCCTGTAATCCCAGCACTTTGGGAGG CTCATTAAAGAATCTGGGAGGCTGGGTGCAGTCGCTCACGCCTGTAATCCCAGCACTTTGGGAGG T G NMRAL1 Ensembl:ENSG00000153406 Protein coding intron GSE38233;GSE100210;GSE99789;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,29796672,31158229 RNA-Seq:(High) rs1387632319 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104600,RMVar_hsa_circ_108642,RMVar_hsa_circ_176009,RMVar_hsa_circ_176010 17219 RMVar_ID_17219 Human_SNP_ID_591953645 A-to-I Human chr16 - 4467390 4467390 4467390 GTCTCTACAAAAAATACAAAAATTAGCCAGGCATGGTGGCGGGCACCTGTAGTCCCAGCGACTCA GTCTCTACAAAAAATACAAAAATTAGCCAGGCGTGGTGGCGGGCACCTGTAGTCCCAGCGACTCA T C NMRAL1 Ensembl:ENSG00000153406 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs753341883 Functional Loss SNV dbSNP153 33..33 33 - - - 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 17220 RMVar_ID_17220 Human_SNP_ID_591953796 A-to-I Human chr16 - 4467892 4467892 4467892 AAATCAGCTGGGCACAGTGGCTCATGCTTGTAATCCCCACACTTTGGGAGGCCGAGGCGGGCAGA AAATCAGCTGGGCACAGTGGCTCATGCTTGTATTCCCCACACTTTGGGAGGCCGAGGCGGGCAGA T A NMRAL1 Ensembl:ENSG00000153406 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1327478871 Functional Loss SNV dbSNP153 33..33 33 - - - 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 17221 RMVar_ID_17221 Human_SNP_ID_591953864 A-to-I Human chr16 - 4468107 4468107 4468107 TTAGTACAGACGGGGTTTCTCCATGTTGGTCAAGCTGGTCTCTAACTCCCGGCCTCAGGCGATCC TTAGTACAGACGGGGTTTCTCCATGTTGGTCATGCTGGTCTCTAACTCCCGGCCTCAGGCGATCC T A NMRAL1 Ensembl:ENSG00000153406 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs949797567 Functional Loss SNV dbSNP153 33..33 33 - - - 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 17222 RMVar_ID_17222 Human_SNP_ID_591953865 A-to-I Human chr16 - 4468107 4468107 4468107 TTAGTACAGACGGGGTTTCTCCATGTTGGTCAAGCTGGTCTCTAACTCCCGGCCTCAGGCGATCC TTAGTACAGACGGGGTTTCTCCATGTTGGTCAGGCTGGTCTCTAACTCCCGGCCTCAGGCGATCC T C NMRAL1 Ensembl:ENSG00000153406 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs949797567 Functional Loss SNV dbSNP153 33..33 33 - - - 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 17223 RMVar_ID_17223 Human_SNP_ID_591953910 A-to-I Human chr16 - 4468255 4468255 4468255 TTTTGTTGCCCAGGCTGGCATGCAATGGCGCAATCTTGGCTCACCGCAACCTCCGCCTCCTGGGT TTTTGTTGCCCAGGCTGGCATGCAATGGCGCAGTCTTGGCTCACCGCAACCTCCGCCTCCTGGGT T C NMRAL1 Ensembl:ENSG00000153406 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1475950148 Functional Loss SNV dbSNP153 33..33 33 - - - 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 17224 RMVar_ID_17224 Human_SNP_ID_591953915 A-to-I Human chr16 - 4468263 4468263 4468263 AGTTTCGCTTTTGTTGCCCAGGCTGGCATGCAATGGCGCAATCTTGGCTCACCGCAACCTCCGCC AGTTTCGCTTTTGTTGCCCAGGCTGGCATGCAGTGGCGCAATCTTGGCTCACCGCAACCTCCGCC T C NMRAL1 Ensembl:ENSG00000153406 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs916911895 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12737643 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 17225 RMVar_ID_17225 Human_SNP_ID_591954003 A-to-I Human chr16 - 4468529 4468529 4468529 TCACTGCAACCTCTGCCTCCCAGATTCAAGCAATTCTTCTGCCTCAGCCTCCCGAGTAGCTGGGA TCACTGCAACCTCTGCCTCCCAGATTCAAGCAGTTCTTCTGCCTCAGCCTCCCGAGTAGCTGGGA T C NMRAL1 Ensembl:ENSG00000153406 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs746952120 Functional Loss SNV dbSNP153 33..33 33 - - - 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 17226 RMVar_ID_17226 Human_SNP_ID_591954483 A-to-I Human chr16 - 4469678 4469678 4469678 ATTTTTTGATAGAGGCGGGGTTTCACCAAGCCAAGATCGTGCCACTGCACTTCAGCCTGGGTGAT ATTTTTTGATAGAGGCGGGGTTTCACCAAGCCCAGATCGTGCCACTGCACTTCAGCCTGGGTGAT T G NMRAL1 Ensembl:ENSG00000153406 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1304331393 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1672150,Human_Splice_Rec_1672198 RMVar_hsa_circ_104600,RMVar_hsa_circ_108642,RMVar_hsa_circ_176009,RMVar_hsa_circ_176010,RMVar_hsa_circ_176011,RMVar_hsa_circ_369689 17227 RMVar_ID_17227 Human_SNP_ID_591955461 A-to-I Human chr16 - 4472661 4472661 4472661 CTGCTCACTGCAACTTCTGCCACTCGGGTTCAAGCGATTCTCCTGTCTCACCCTCCTGAGTAGCA CTGCTCACTGCAACTTCTGCCACTCGGGTTCAGGCGATTCTCCTGTCTCACCCTCCTGAGTAGCA T C NMRAL1 Ensembl:ENSG00000153406 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1029971692 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104600,RMVar_hsa_circ_108642,RMVar_hsa_circ_176009,RMVar_hsa_circ_176010,RMVar_hsa_circ_176011,RMVar_hsa_circ_369689 17228 RMVar_ID_17228 Human_SNP_ID_591955613 A-to-I Human chr16 - 4473076 4473076 4473076 ATAGCTACCTAGGAGGTTGAGGTGGGAGGATCACCTGAGTCCAGCAGGTCAAGGCTGCAGTGACC ATAGCTACCTAGGAGGTTGAGGTGGGAGGATCGCCTGAGTCCAGCAGGTCAAGGCTGCAGTGACC T C NMRAL1 Ensembl:ENSG00000153406 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1051401545 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12737705 RMVar_hsa_circ_104600,RMVar_hsa_circ_108642,RMVar_hsa_circ_176009,RMVar_hsa_circ_176010,RMVar_hsa_circ_176011,RMVar_hsa_circ_369689 17229 RMVar_ID_17229 Human_SNP_ID_591956435 A-to-I Human chr16 + 4475546 4475546 4475546 GCTGGCCAGGCTGGTCTCGAACTGCTGACCTCAAGTGATCTTCCCGCCTCAGGCTCCCAAAGTGC GCTGGCCAGGCTGGTCTCGAACTGCTGACCTCTAGTGATCTTCCCGCCTCAGGCTCCCAAAGTGC A T HMOX2 Ensembl:ENSG00000103415 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1237931070 Functional Loss SNV dbSNP153 33..33 33 - - - 17230 RMVar_ID_17230 Human_SNP_ID_591960261 A-to-I Human chr16 + 4487160 4487159 4487161 GAATGCCTGTAGTCTCAGCTGCTCGAGAGGCTAAGTTGGAAGTATCACCTGAGCCCAGGAGTTGA GAATGCCTGTAGTCTCAGCTGCTCGAGAGGCT__GTTGGAAGTATCACCTGAGCCCAGGAGTTGA TAA T HMOX2 Ensembl:ENSG00000103415 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1266552446 Functional Loss DEL dbSNP153 33..34 33 - - - 17231 RMVar_ID_17231 Human_SNP_ID_591960861 A-to-I Human chr16 + 4488955 4488955 4488955 TCAAGCAATCCTCCTGCCTAGGACTCCTGAGTAGCTGGGATGACAGGCATGTGCCACCACGCCCA TCAAGCAATCCTCCTGCCTAGGACTCCTGAGTGGCTGGGATGACAGGCATGTGCCACCACGCCCA A G HMOX2 Ensembl:ENSG00000103415 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1161217413 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12737867 17232 RMVar_ID_17232 Human_SNP_ID_591960993 A-to-I Human chr16 + 4489426 4489426 4489426 TCCGCCTCAGCCTCGCGAGTAGCTGGGACCACAAGCACTCACCACCACATCCAGCTAGTTTTATT TCCGCCTCAGCCTCGCGAGTAGCTGGGACCACCAGCACTCACCACCACATCCAGCTAGTTTTATT A C HMOX2 Ensembl:ENSG00000103415 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170068930 Functional Loss SNV dbSNP153 33..33 33 - - - 17233 RMVar_ID_17233 Human_SNP_ID_591961937 A-to-I Human chr16 + 4493046 4493046 4493046 TTTTCTTTTCTCTTCTTTTTCCTCTTTTTTTGAGACAGAGTCTCGCTCTGTGGCCCAGGCTGGAA TTTTCTTTTCTCTTCTTTTTCCTCTTTTTTTGGGACAGAGTCTCGCTCTGTGGCCCAGGCTGGAA A G HMOX2 Ensembl:ENSG00000103415 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1212654202 Functional Loss SNV dbSNP153 33..33 33 - - - 17234 RMVar_ID_17234 Human_SNP_ID_591962233 A-to-I Human chr16 + 4494205 4494205 4494205 GGGCGTGGTGGTGGGCGCCTGTAGTCTCAGCTACTCAGGAGGCTGAGGCAGGAGAATGGCATGAA GGGCGTGGTGGTGGGCGCCTGTAGTCTCAGCTCCTCAGGAGGCTGAGGCAGGAGAATGGCATGAA A C HMOX2 Ensembl:ENSG00000103415 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1479495581 Functional Loss SNV dbSNP153 33..33 33 - - - 17235 RMVar_ID_17235 Human_SNP_ID_591968708 A-to-I Human chr16 - 4517557 4517556 4517557 AATTTTTCTTTTGTAGAGACAAGAGTCTTGCCATGTTGACCATGCTGGTTTCGAACCCCTGGCCT AATTTTTCTTTTGTAGAGACAAGAGTCTTGCC_TGTTGACCATGCTGGTTTCGAACCCCTGGCCT AT A CDIP1 Ensembl:ENSG00000089486 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1261572898 Functional Loss DEL dbSNP153 33..33 33 - - - 17236 RMVar_ID_17236 Human_SNP_ID_591968735 A-to-I Human chr16 - 4517659 4517659 4517659 ATGGCTCACTGTATCCTCTGAGTCTTGGGCTCAGGTGATCCTCCTGCCTCAGCCTCCCCAGTAGC ATGGCTCACTGTATCCTCTGAGTCTTGGGCTCTGGTGATCCTCCTGCCTCAGCCTCCCCAGTAGC T A CDIP1 Ensembl:ENSG00000089486 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1236358600 Functional Loss SNV dbSNP153 33..33 33 - - - 17237 RMVar_ID_17237 Human_SNP_ID_591969428 A-to-I Human chr16 - 4520250 4520250 4520250 AAATACAAAAATTAGATGGGTGGCATGCCTGTAGTCCCAGCTCCTCAGGAGGCTGAGGCAGGAGA AAATACAAAAATTAGATGGGTGGCATGCCTGTGGTCCCAGCTCCTCAGGAGGCTGAGGCAGGAGA T C CDIP1 Ensembl:ENSG00000089486 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs995817961 Functional Loss SNV dbSNP153 33..33 33 - - - 17238 RMVar_ID_17238 Human_SNP_ID_591971165 A-to-I Human chr16 - 4526386 4526386 4526386 ATTTTTTATATTTTGAGACAGATTCTCAGACTATTGCCCGGGCTGGAGTGCGACGGTGTGATCTC ATTTTTTATATTTTGAGACAGATTCTCAGACTGTTGCCCGGGCTGGAGTGCGACGGTGTGATCTC T C CDIP1 Ensembl:ENSG00000089486 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1413650467 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12738137 17239 RMVar_ID_17239 Human_SNP_ID_591971166 A-to-I Human chr16 - 4526386 4526386 4526386 ATTTTTTATATTTTGAGACAGATTCTCAGACTATTGCCCGGGCTGGAGTGCGACGGTGTGATCTC ATTTTTTATATTTTGAGACAGATTCTCAGACTCTTGCCCGGGCTGGAGTGCGACGGTGTGATCTC T G CDIP1 Ensembl:ENSG00000089486 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1413650467 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12738137 17240 RMVar_ID_17240 Human_SNP_ID_591995821 A-to-I Human chr16 - 4605850 4605850 4605850 TAGAGATAGGGTCTTGCTCTGTTCCCCAGACTAGAGTGCAGTGATGCAATCATAGCTCACTACAG TAGAGATAGGGTCTTGCTCTGTTCCCCAGACTGGAGTGCAGTGATGCAATCATAGCTCACTACAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs538184465 Functional Loss SNV dbSNP153 33..33 33 - - - 17241 RMVar_ID_17241 Human_SNP_ID_592003811 A-to-I Human chr16 + 4628662 4628662 4628662 CGCCTCCTGGGTTCAAGCAATTCTCCTGTTTCAGCCTCCTGAGTAGCTTGGATTACAGGTGCGCA CGCCTCCTGGGTTCAAGCAATTCTCCTGTTTCGGCCTCCTGAGTAGCTTGGATTACAGGTGCGCA A G MGRN1 Ensembl:ENSG00000102858 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1378730089 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119059,RMVar_hsa_circ_176024 17242 RMVar_ID_17242 Human_SNP_ID_592004463 A-to-I Human chr16 + 4630191 4630191 4630191 CTGGGCAACATGGTGAAACTCCATGTCTCCTAAAATACAAAAAATTAGTTGGGTGTGGCAGCATG CTGGGCAACATGGTGAAACTCCATGTCTCCTACAATACAAAAAATTAGTTGGGTGTGGCAGCATG A C MGRN1 Ensembl:ENSG00000102858 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1332953819 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119059,RMVar_hsa_circ_176024 17243 RMVar_ID_17243 Human_SNP_ID_592004742 A-to-I Human chr16 + 4630994 4630994 4630994 ATGTGTACCACTATGCCCAGCAAAGTTTTTGTATTTTTTTTGTAGAGACAGGGTTTCACCGTGTT ATGTGTACCACTATGCCCAGCAAAGTTTTTGTGTTTTTTTTGTAGAGACAGGGTTTCACCGTGTT A G MGRN1 Ensembl:ENSG00000102858 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs931617110 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12739715 RMVar_hsa_circ_119059,RMVar_hsa_circ_176024 17244 RMVar_ID_17244 Human_SNP_ID_592005544 A-to-I Human chr16 + 4633505 4633505 4633505 CCTGAGGTCGGAGGTTTGAGACCAGACTGACCAAGATGGAGAAGCCCCATCTCTACTAAAAATAC CCTGAGGTCGGAGGTTTGAGACCAGACTGACCGAGATGGAGAAGCCCCATCTCTACTAAAAATAC A G MGRN1 Ensembl:ENSG00000102858 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1430918409 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119059,RMVar_hsa_circ_176024 17245 RMVar_ID_17245 Human_SNP_ID_592020686 A-to-I Human chr16 + 4670312 4670312 4670312 TCGCCGAGGCTGGAGTGCAGTGGCATGATCCCAGCTTACTGTAGCCTCCACCTCCTGGGTTCAAG TCGCCGAGGCTGGAGTGCAGTGGCATGATCCCGGCTTACTGTAGCCTCCACCTCCTGGGTTCAAG A G MGRN1 Ensembl:ENSG00000102858 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1001700854 Functional Loss SNV dbSNP153 33..33 33 - - - 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 17246 RMVar_ID_17246 Human_SNP_ID_592040942 A-to-I Human chr16 - 4716863 4716863 4716863 TCGTCGAGGCTGTAGTGCAGTGGCGCGATCTCAGCTCACTGCAACCTCCGCCTCCTGGATTCAAG TCGTCGAGGCTGTAGTGCAGTGGCGCGATCTCGGCTCACTGCAACCTCCGCCTCCTGGATTCAAG T C ANKS3 Ensembl:ENSG00000168096 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1375415279 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268251,RMVar_hsa_circ_37489,RMVar_hsa_circ_309244,RMVar_hsa_circ_18417,RMVar_hsa_circ_1600,RMVar_hsa_circ_176047,RMVar_hsa_circ_176049,RMVar_hsa_circ_329675,RMVar_hsa_circ_332563,RMVar_hsa_circ_37118,RMVar_hsa_circ_176050 17247 RMVar_ID_17247 Human_SNP_ID_592043236 A-to-I Human chr16 - 4722835 4722835 4722835 CGGCTCACTGCAACCTCTACCTCCCAAGTTCAAGCAGTTCTTCTGCCTCAGCCTCCCGAGTAGCT CGGCTCACTGCAACCTCTACCTCCCAAGTTCAGGCAGTTCTTCTGCCTCAGCCTCCCGAGTAGCT T C ANKS3 Ensembl:ENSG00000168096 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs547527493 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268251,RMVar_hsa_circ_37489,RMVar_hsa_circ_309244,RMVar_hsa_circ_18417,RMVar_hsa_circ_1600,RMVar_hsa_circ_176047,RMVar_hsa_circ_176049,RMVar_hsa_circ_329675,RMVar_hsa_circ_332563,RMVar_hsa_circ_37118,RMVar_hsa_circ_176050 17248 RMVar_ID_17248 Human_SNP_ID_592046299 A-to-I Human chr16 - 4731404 4731404 4731404 ATGATGGCGCACACCTGTAATCTCAGCTATTCAGGTGGCTGAGGCTCAAGAAGCCCTTAAACCCA ATGATGGCGCACACCTGTAATCTCAGCTATTCGGGTGGCTGAGGCTCAAGAAGCCCTTAAACCCA T C ANKS3,AC020663.1 Ensembl:ENSG00000168096,Ensembl:ENSG00000266994 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1035817556 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268251,RMVar_hsa_circ_329554 17249 RMVar_ID_17249 Human_SNP_ID_592046300 A-to-I Human chr16 - 4731404 4731404 4731404 ATGATGGCGCACACCTGTAATCTCAGCTATTCAGGTGGCTGAGGCTCAAGAAGCCCTTAAACCCA ATGATGGCGCACACCTGTAATCTCAGCTATTCCGGTGGCTGAGGCTCAAGAAGCCCTTAAACCCA T G ANKS3,AC020663.1 Ensembl:ENSG00000168096,Ensembl:ENSG00000266994 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1035817556 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268251,RMVar_hsa_circ_329554 17250 RMVar_ID_17250 Human_SNP_ID_592054262 A-to-I Human chr16 - 4753340 4753340 4753340 CTCCGACCTCAGCCTCCTGAGTAGCTAGGACTACAGGCACACGCCACCATGCCCAGCTAGTTTTG CTCCGACCTCAGCCTCCTGAGTAGCTAGGACTCCAGGCACACGCCACCATGCCCAGCTAGTTTTG T G ZNF500 Ensembl:ENSG00000103199 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs932139183 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19000 17251 RMVar_ID_17251 Human_SNP_ID_592055308 A-to-I Human chr16 - 4756744 4756744 4756744 TGGGAGGCCAAGGCGGGTGGATCACGAGGTCAAGAGATCGAGACCATCCTGGCCGGCATGGTGAA TGGGAGGCCAAGGCGGGTGGATCACGAGGTCAGGAGATCGAGACCATCCTGGCCGGCATGGTGAA T C ZNF500 Ensembl:ENSG00000103199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs371130477 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19000 17252 RMVar_ID_17252 Human_SNP_ID_592055803 A-to-I Human chr16 - 4758125 4758125 4758125 GAAGCCGAGGCGAGTGTTTATCACCTGAGGTCAGGAGTTCGAGTCCAGCCTGGCCAACATGGTGA GAAGCCGAGGCGAGTGTTTATCACCTGAGGTCGGGAGTTCGAGTCCAGCCTGGCCAACATGGTGA T C ZNF500 Ensembl:ENSG00000103199 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1265297942 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19000 17253 RMVar_ID_17253 Human_SNP_ID_592075913 A-to-I Human chr16 - 4806395 4806395 4806395 CCATGATCCTACCACTGCACTCCAGCCTGGGCAACAGAGCAAGACCCTGTCTCAAGAAAAAAAAA CCATGATCCTACCACTGCACTCCAGCCTGGGCGACAGAGCAAGACCCTGTCTCAAGAAAAAAAAA T C GLYR1 Ensembl:ENSG00000140632 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs373691644 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75995,RMVar_hsa_circ_176058 17254 RMVar_ID_17254 Human_SNP_ID_592075917 A-to-I Human chr16 - 4806432 4806432 4806432 GGATTGCTTGAGCCCAGGAGTTCGAGGCTGCAATGAGCCATGATCCTACCACTGCACTCCAGCCT GGATTGCTTGAGCCCAGGAGTTCGAGGCTGCATTGAGCCATGATCCTACCACTGCACTCCAGCCT T A GLYR1 Ensembl:ENSG00000140632 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1294378553 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75995,RMVar_hsa_circ_176058 17255 RMVar_ID_17255 Human_SNP_ID_592075918 A-to-I Human chr16 - 4806432 4806432 4806432 GGATTGCTTGAGCCCAGGAGTTCGAGGCTGCAATGAGCCATGATCCTACCACTGCACTCCAGCCT GGATTGCTTGAGCCCAGGAGTTCGAGGCTGCAGTGAGCCATGATCCTACCACTGCACTCCAGCCT T C GLYR1 Ensembl:ENSG00000140632 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1294378553 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75995,RMVar_hsa_circ_176058 17256 RMVar_ID_17256 Human_SNP_ID_592075969 A-to-I Human chr16 - 4806567 4806567 4806567 GCCCAGGAGTTTGAGACCAGCCTGGGCAACATAGCAAGACCCCCATCTGTACAAAAAAAAATAAA GCCCAGGAGTTTGAGACCAGCCTGGGCAACATGGCAAGACCCCCATCTGTACAAAAAAAAATAAA T C GLYR1 Ensembl:ENSG00000140632 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1036732154 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75995,RMVar_hsa_circ_176058 17257 RMVar_ID_17257 Human_SNP_ID_592076752 A-to-I Human chr16 - 4808516 4808516 4808516 TCGGCTCACTGCAACCTCTGCCTCCTGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCACAGTAGC TCGGCTCACTGCAACCTCTGCCTCCTGGGTTCTAGTGATTCTCCTGCCTCAGCCTCCACAGTAGC T A GLYR1 Ensembl:ENSG00000140632 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1365046678 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75995,RMVar_hsa_circ_176058 17258 RMVar_ID_17258 Human_SNP_ID_592077051 A-to-I Human chr16 - 4809242 4809242 4809242 GAGGTTGCAGTGAGCCTAGATCGCACCACTGCACTCCAGCCTGGGCAACAGAGTGAGACTCCATC GAGGTTGCAGTGAGCCTAGATCGCACCACTGCGCTCCAGCCTGGGCAACAGAGTGAGACTCCATC T C GLYR1 Ensembl:ENSG00000140632 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1011537911 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75995,RMVar_hsa_circ_176058 17259 RMVar_ID_17259 Human_SNP_ID_592077052 A-to-I Human chr16 - 4809242 4809242 4809242 GAGGTTGCAGTGAGCCTAGATCGCACCACTGCACTCCAGCCTGGGCAACAGAGTGAGACTCCATC GAGGTTGCAGTGAGCCTAGATCGCACCACTGCCCTCCAGCCTGGGCAACAGAGTGAGACTCCATC T G GLYR1 Ensembl:ENSG00000140632 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1011537911 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75995,RMVar_hsa_circ_176058 17260 RMVar_ID_17260 Human_SNP_ID_592077054 A-to-I Human chr16 - 4809250 4809250 4809250 GGAGGCGGGAGGTTGCAGTGAGCCTAGATCGCACCACTGCACTCCAGCCTGGGCAACAGAGTGAG GGAGGCGGGAGGTTGCAGTGAGCCTAGATCGCCCCACTGCACTCCAGCCTGGGCAACAGAGTGAG T G GLYR1 Ensembl:ENSG00000140632 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1462259235 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75995,RMVar_hsa_circ_176058 17261 RMVar_ID_17261 Human_SNP_ID_592077122 A-to-I Human chr16 - 4809444 4809444 4809444 CCATGCCTGGCTAATTTTTTGTATTTTTAGTAAAGACGGGGTTCCACTGTGTTAGCCAGGATGGT CCATGCCTGGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTCCACTGTGTTAGCCAGGATGGT T C GLYR1 Ensembl:ENSG00000140632 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1229195059 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75995,RMVar_hsa_circ_176058 17262 RMVar_ID_17262 Human_SNP_ID_592077126 A-to-I Human chr16 - 4809463 4809463 4809463 GGACTGCAGGCGCCTGCCACCATGCCTGGCTAATTTTTTGTATTTTTAGTAAAGACGGGGTTCCA GGACTGCAGGCGCCTGCCACCATGCCTGGCTAGTTTTTTGTATTTTTAGTAAAGACGGGGTTCCA T C GLYR1 Ensembl:ENSG00000140632 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs556983959 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75995,RMVar_hsa_circ_176058 17263 RMVar_ID_17263 Human_SNP_ID_592077164 A-to-I Human chr16 - 4809568 4809568 4809568 TCGCTCTGTCACCCAAGCTGGAGTACAGTGGCACGATCTCGGCTCACTGCAAGCTTCGTCTCCCG TCGCTCTGTCACCCAAGCTGGAGTACAGTGGCGCGATCTCGGCTCACTGCAAGCTTCGTCTCCCG T C GLYR1 Ensembl:ENSG00000140632 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1384037572 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75995,RMVar_hsa_circ_176058 17264 RMVar_ID_17264 Human_SNP_ID_592077265 A-to-I Human chr16 - 4809812 4809812 4809812 TCAAGCGATTCTCATGCCTCAGCCTCTTGAGTAGCTGGGATTACAGGCACACACCACCATACACA TCAAGCGATTCTCATGCCTCAGCCTCTTGAGTGGCTGGGATTACAGGCACACACCACCATACACA T C GLYR1 Ensembl:ENSG00000140632 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1181125898 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75995,RMVar_hsa_circ_176058 17265 RMVar_ID_17265 Human_SNP_ID_592077437 A-to-I Human chr16 - 4810240 4810240 4810240 CACCTGCCTCAGCCTCTCAAAGTGCTGGGATTACAGGTGTGAGCCACTGTGTCTGGCCTCTTTGT CACCTGCCTCAGCCTCTCAAAGTGCTGGGATTTCAGGTGTGAGCCACTGTGTCTGGCCTCTTTGT T A GLYR1 Ensembl:ENSG00000140632 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1446495395 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75995,RMVar_hsa_circ_176058 17266 RMVar_ID_17266 Human_SNP_ID_592077467 A-to-I Human chr16 - 4810314 4810314 4810314 TTTTGTATTTTTAGTAGAGATGGGGTTTTGCCATGTTGGCTAGGCTGTTCTCCAACTCCTGACCT TTTTGTATTTTTAGTAGAGATGGGGTTTTGCCGTGTTGGCTAGGCTGTTCTCCAACTCCTGACCT T C GLYR1 Ensembl:ENSG00000140632 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs777963683 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75995,RMVar_hsa_circ_176058 17267 RMVar_ID_17267 Human_SNP_ID_592077808 A-to-I Human chr16 - 4811074 4811074 4811074 TTTTAACGGAGTCTCACTCTGTCACCCAGGCTAGAGTGCACTGGTGCGATCTCAGCTCAATGCAA TTTTAACGGAGTCTCACTCTGTCACCCAGGCTGGAGTGCACTGGTGCGATCTCAGCTCAATGCAA T C GLYR1 Ensembl:ENSG00000140632 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs561801436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19076654 RMVar_hsa_circ_75995,RMVar_hsa_circ_176058 17268 RMVar_ID_17268 Human_SNP_ID_592087940 A-to-I Human chr16 - 4838660 4838660 4838660 ATGGCGTGAACCCCAGAGGCAGAGCTTGCCGTAAGTCGAGATCGCGCCACTGCACTCCAGCCTGG ATGGCGTGAACCCCAGAGGCAGAGCTTGCCGTGAGTCGAGATCGCGCCACTGCACTCCAGCCTGG T C GLYR1 Ensembl:ENSG00000140632 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs952727656 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25244762 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 17269 RMVar_ID_17269 Human_SNP_ID_592089335 A-to-I Human chr16 - 4842466 4842466 4842466 ACACAAGTGTAGTCCCAGGTATGCAGAAGGCTAAGGCAGGAGGATTGCTTGAGCCCAGGAGGTCA ACACAAGTGTAGTCCCAGGTATGCAGAAGGCTTAGGCAGGAGGATTGCTTGAGCCCAGGAGGTCA T A GLYR1 Ensembl:ENSG00000140632 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs769296967 Functional Loss SNV dbSNP153 33..33 33 - - - 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 17270 RMVar_ID_17270 Human_SNP_ID_592089336 A-to-I Human chr16 - 4842466 4842466 4842466 ACACAAGTGTAGTCCCAGGTATGCAGAAGGCTAAGGCAGGAGGATTGCTTGAGCCCAGGAGGTCA ACACAAGTGTAGTCCCAGGTATGCAGAAGGCTGAGGCAGGAGGATTGCTTGAGCCCAGGAGGTCA T C GLYR1 Ensembl:ENSG00000140632 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs769296967 Functional Loss SNV dbSNP153 33..33 33 - - - 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 17271 RMVar_ID_17271 Human_SNP_ID_592089596 A-to-I Human chr16 - 4843247 4843247 4843247 GGGAGGCTGAGGCTCGAGAATTGCCTGAACCCAGGAGGCAGAGATTGTTCGAGACCCTGCACTCC GGGAGGCTGAGGCTCGAGAATTGCCTGAACCCTGGAGGCAGAGATTGTTCGAGACCCTGCACTCC T A GLYR1 Ensembl:ENSG00000140632 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1004296032 Functional Loss SNV dbSNP153 33..33 33 - - - 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 17272 RMVar_ID_17272 Human_SNP_ID_592092052 A-to-I Human chr16 + 4849074 4849074 4849074 GTGAGCCGAGATTATGTCACTGCACTCCAGCTAGGCGACAGAGCGAGCGAGACTCGTCCCCCCGC GTGAGCCGAGATTATGTCACTGCACTCCAGCTGGGCGACAGAGCGAGCGAGACTCGTCCCCCCGC A G UBN1 Ensembl:ENSG00000118900 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1186733499 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76543,RMVar_hsa_circ_176075 17273 RMVar_ID_17273 Human_SNP_ID_592093777 A-to-I Human chr16 + 4853613 4853613 4853613 CGAGTCTCGCCCTGTCGTCCAGGCTGGAATGCAATGGGGCGATCTCGGCTCACTGTAACCTCCGC CGAGTCTCGCCCTGTCGTCCAGGCTGGAATGCCATGGGGCGATCTCGGCTCACTGTAACCTCCGC A C UBN1 Ensembl:ENSG00000118900 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1423967693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12747558 RMVar_hsa_circ_59584,RMVar_hsa_circ_338876,RMVar_hsa_circ_8184,RMVar_hsa_circ_176076 17274 RMVar_ID_17274 Human_SNP_ID_592095100 A-to-I Human chr16 + 4857243 4857243 4857243 ATAGTGTTGTATGCCTATAGTCCCAGCTATTCAGGAGGCTGAGGCAGGAGGATCACCCGAGCCTG ATAGTGTTGTATGCCTATAGTCCCAGCTATTCGGGAGGCTGAGGCAGGAGGATCACCCGAGCCTG A G UBN1 Ensembl:ENSG00000118900 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs751847599 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59584,RMVar_hsa_circ_338876,RMVar_hsa_circ_8184,RMVar_hsa_circ_176076 17275 RMVar_ID_17275 Human_SNP_ID_592098054 A-to-I Human chr16 + 4865979 4865979 4865979 ACAAGACTCCGTCTCAAAAACTAAACTAAAATAAAAAAATAAAAAATAATAAGATAAAATTTGAT ACAAGACTCCGTCTCAAAAACTAAACTAAAATGAAAAAATAAAAAATAATAAGATAAAATTTGAT A G UBN1 Ensembl:ENSG00000118900 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1382818884 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8184,RMVar_hsa_circ_39825 17276 RMVar_ID_17276 Human_SNP_ID_592115873 A-to-I Human chr16 - 4912207 4912207 4912207 CTGGTTGCCAGGGGCTGGAGCGGGTGGGGAATAGGGAGTGACAGCTTGTGGGTGTGGAGCTTTGG CTGGTTGCCAGGGGCTGGAGCGGGTGGGGAATCGGGAGTGACAGCTTGTGGGTGTGGAGCTTTGG T G PPL Ensembl:ENSG00000118898 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909231556 Functional Loss SNV dbSNP153 33..33 33 - - - 17277 RMVar_ID_17277 Human_SNP_ID_592118626 A-to-I Human chr16 - 4920565 4920565 4920565 CCAGCTACTCGGGAGGCTGAGGCAGTAGAATCACTTGAATCCAGAGACGGAGGTTGCAGTGAGCC CCAGCTACTCGGGAGGCTGAGGCAGTAGAATCGCTTGAATCCAGAGACGGAGGTTGCAGTGAGCC T C PPL Ensembl:ENSG00000118898 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1266086857 Functional Loss SNV dbSNP153 33..33 33 - - - 17278 RMVar_ID_17278 Human_SNP_ID_592132462 A-to-I Human chr16 + 4961503 4961503 4961503 GATGCACACCACCATGCCCAGGTAATTTTTGTATTTTCAGTATAGACGGGGTTTCATCACGTTGG GATGCACACCACCATGCCCAGGTAATTTTTGTGTTTTCAGTATAGACGGGGTTTCATCACGTTGG A G SEC14L5 Ensembl:ENSG00000103184 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1331262283 Functional Loss SNV dbSNP153 33..33 33 - - - 17279 RMVar_ID_17279 Human_SNP_ID_592150198 A-to-I Human chr16 + 5009533 5009533 5009533 TTTTGTAGAGATGGGGTCTTGCTATGTTGCCCAGGATGATCTTGAATGCCTGAGCTCAAGCGATC TTTTGTAGAGATGGGGTCTTGCTATGTTGCCCGGGATGATCTTGAATGCCTGAGCTCAAGCGATC A G SEC14L5 Ensembl:ENSG00000103184 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1394130197 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12151 17280 RMVar_ID_17280 Human_SNP_ID_592156298 A-to-I Human chr16 - 5026045 5026045 5026045 TCGAGCCTGTAGTCCCAGCTACTCGGGAGTCCAAGGCAGGGGAATCGTTTGAAGCCAGGAGGCGG TCGAGCCTGTAGTCCCAGCTACTCGGGAGTCCGAGGCAGGGGAATCGTTTGAAGCCAGGAGGCGG T C NAGPA Ensembl:ENSG00000103174 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1229617008 Functional Loss SNV dbSNP153 33..33 33 - - - 17281 RMVar_ID_17281 Human_SNP_ID_592157427 A-to-I Human chr16 - 5028840 5028840 5028840 CGTGAGAGCCGCCTTCGTGAGGGCTGAAGTCCAGGTCTGCCCCAGCCTGTCTCATTCAGCCAATA CGTGAGAGCCGCCTTCGTGAGGGCTGAAGTCCTGGTCTGCCCCAGCCTGTCTCATTCAGCCAATA T A NAGPA Ensembl:ENSG00000103174 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1995278 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19070822 RMVar_hsa_circ_52592,RMVar_hsa_circ_354914,RMVar_hsa_circ_176086 17282 RMVar_ID_17282 Human_SNP_ID_592157428 A-to-I Human chr16 - 5028840 5028840 5028840 CGTGAGAGCCGCCTTCGTGAGGGCTGAAGTCCAGGTCTGCCCCAGCCTGTCTCATTCAGCCAATA CGTGAGAGCCGCCTTCGTGAGGGCTGAAGTCCGGGTCTGCCCCAGCCTGTCTCATTCAGCCAATA T C NAGPA Ensembl:ENSG00000103174 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1995278 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19070822 RMVar_hsa_circ_52592,RMVar_hsa_circ_354914,RMVar_hsa_circ_176086 17283 RMVar_ID_17283 Human_SNP_ID_592157429 A-to-I Human chr16 - 5028840 5028840 5028840 CGTGAGAGCCGCCTTCGTGAGGGCTGAAGTCCAGGTCTGCCCCAGCCTGTCTCATTCAGCCAATA CGTGAGAGCCGCCTTCGTGAGGGCTGAAGTCCCGGTCTGCCCCAGCCTGTCTCATTCAGCCAATA T G NAGPA Ensembl:ENSG00000103174 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1995278 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19070822 RMVar_hsa_circ_52592,RMVar_hsa_circ_354914,RMVar_hsa_circ_176086 17284 RMVar_ID_17284 Human_SNP_ID_592177824 A-to-I Human chr16 - 5085978 5085978 5085978 TGCTTCTGTCCCGCTGTGCCAAGTGCTGGGGCAGACACAGGCAGAGAGTGGACAGCGGCACGGTG TGCTTCTGTCCCGCTGTGCCAAGTGCTGGGGCGGACACAGGCAGAGAGTGGACAGCGGCACGGTG T C EEF2KMT Ensembl:ENSG00000118894 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4238853 Functional Loss SNV dbSNP153 33..33 33 - - - 17285 RMVar_ID_17285 Human_SNP_ID_592188151 A-to-I Human chr16 + 5113534 5113534 5113534 AAAAATTAGCTGGGTTGGTGGTGAATGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAAG AAAAATTAGCTGGGTTGGTGGTGAATGCCTGTGGTCCCAGCTACTCGGGAGGCTGAGGCAGGAAG A G AC026458.2,AC074051.4 Ensembl:ENSG00000267070,Ensembl:ENSG00000285567 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404922504 Functional Loss SNV dbSNP153 33..33 33 - - - 17286 RMVar_ID_17286 Human_SNP_ID_592552803 A-to-I Human chr16 + 6054948 6054948 6054948 GGGACTGCAGGTGTGTGCCACTATGCTTGGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTC GGGACTGCAGGTGTGTGCCACTATGCTTGGCTGATTTTTTGTATTTTTAGTAGAGACGGGGTTTC A G RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1175440377 Functional Loss SNV dbSNP153 33..33 33 - - - 17287 RMVar_ID_17287 Human_SNP_ID_592560280 A-to-I Human chr16 + 6074200 6074200 6074200 TTGACCTTCTGACCTTGTGATCCGCCCGCCTCAGCCTACCAAAGTGCTGGGATTACAGGCATGAG TTGACCTTCTGACCTTGTGATCCGCCCGCCTCCGCCTACCAAAGTGCTGGGATTACAGGCATGAG A C AC009135.1,RBFOX1 Ensembl:ENSG00000257180,Ensembl:ENSG00000078328 lincRNA,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs762540227 Functional Loss SNV dbSNP153 33..33 33 - - - 17288 RMVar_ID_17288 Human_SNP_ID_592560285 A-to-I Human chr16 + 6074209 6074209 6074209 TGACCTTGTGATCCGCCCGCCTCAGCCTACCAAAGTGCTGGGATTACAGGCATGAGCCACAGCGC TGACCTTGTGATCCGCCCGCCTCAGCCTACCAGAGTGCTGGGATTACAGGCATGAGCCACAGCGC A G AC009135.1,RBFOX1 Ensembl:ENSG00000257180,Ensembl:ENSG00000078328 lincRNA,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs565305219 Functional Loss SNV dbSNP153 33..33 33 - - - 17289 RMVar_ID_17289 Human_SNP_ID_592577087 A-to-I Human chr16 + 6117662 6117662 6117662 GTAGCTTTCACTCAACAACTGAGCCTGCTGGCACCTAGGTCTTGAACTTCCCAGCCTCCAGAACT GTAGCTTTCACTCAACAACTGAGCCTGCTGGCCCCTAGGTCTTGAACTTCCCAGCCTCCAGAACT A C RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1320337587 Functional Loss SNV dbSNP153 33..33 33 - - - 17290 RMVar_ID_17290 Human_SNP_ID_592662545 A-to-I Human chr16 + 6342419 6342419 6342419 GTTTTGCCATGGCAATCTTTTCACATTGAATGAATACAAAACGTCAAGGTGCTTAGCATAGACTA GTTTTGCCATGGCAATCTTTTCACATTGAATGCATACAAAACGTCAAGGTGCTTAGCATAGACTA A C RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1014115419 Functional Loss SNV dbSNP153 33..33 33 - - - 17291 RMVar_ID_17291 Human_SNP_ID_592800380 A-to-I Human chr16 + 6658418 6658418 6658418 CTTAGTAGAGGTGGGGTTTTACCATGTTGGCCAGGATGATCTTGAACTCCTGACCTCGTGATCCG CTTAGTAGAGGTGGGGTTTTACCATGTTGGCCGGGATGATCTTGAACTCCTGACCTCGTGATCCG A G RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1186635238 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12201 17292 RMVar_ID_17292 Human_SNP_ID_592806213 A-to-I Human chr16 + 6670083 6670083 6670083 TTGCTCTAGTGTCCACGTTGGAGTGCAGTGGTATGATCATGGCTCACTGCAACCTCACCCTCCTG TTGCTCTAGTGTCCACGTTGGAGTGCAGTGGTTTGATCATGGCTCACTGCAACCTCACCCTCCTG A T RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1249574387 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12201 17293 RMVar_ID_17293 Human_SNP_ID_592806259 A-to-I Human chr16 + 6670176 6670176 6670176 GGCATGTTGTACTTACTCAGTGTGATCCTCCTACATCAGCTTCCCAAGTAGCTGGAACCACAGGA GGCATGTTGTACTTACTCAGTGTGATCCTCCTGCATCAGCTTCCCAAGTAGCTGGAACCACAGGA A G RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1297583979 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12201 17294 RMVar_ID_17294 Human_SNP_ID_592808410 A-to-I Human chr16 + 6674505 6674505 6674505 CACCATGCCCGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCGTCATGTTGATCAGGATGG CACCATGCCCGGCTAATTTTTGTATTTTTAGTCGAGACGGGGTTTCGTCATGTTGATCAGGATGG A C RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1224319989 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12201 17295 RMVar_ID_17295 Human_SNP_ID_592808411 A-to-I Human chr16 + 6674505 6674505 6674505 CACCATGCCCGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCGTCATGTTGATCAGGATGG CACCATGCCCGGCTAATTTTTGTATTTTTAGTTGAGACGGGGTTTCGTCATGTTGATCAGGATGG A T RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1224319989 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12201 17296 RMVar_ID_17296 Human_SNP_ID_592810558 A-to-I Human chr16 + 6678376 6678376 6678376 GAACTCCTGACCTCAAGTCATCTACCCAACTCAGCCTCCTAAAGTGCTGGGATTACAGGCATGAG GAACTCCTGACCTCAAGTCATCTACCCAACTCGGCCTCCTAAAGTGCTGGGATTACAGGCATGAG A G RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1056116737 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12201 17297 RMVar_ID_17297 Human_SNP_ID_592819006 A-to-I Human chr16 + 6695151 6695151 6695151 AAAAAGGAAAAAAAACAATGGCCGGGCGCAGTAGCTCATGCCTGAAATCCCAGCACTTTGGGAGG AAAAAGGAAAAAAAACAATGGCCGGGCGCAGTGGCTCATGCCTGAAATCCCAGCACTTTGGGAGG A G RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs566537992 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12201 17298 RMVar_ID_17298 Human_SNP_ID_592829774 A-to-I Human chr16 + 6717989 6717989 6717989 ATAAATTCTGTAGGTGGCCTTCTCTCCCCTGCACCATTTTCTACCACCACCACCGTCATCACCAC ATAAATTCTGTAGGTGGCCTTCTCTCCCCTGCTCCATTTTCTACCACCACCACCGTCATCACCAC A T RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1184931258 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12201 17299 RMVar_ID_17299 Human_SNP_ID_592838174 A-to-I Human chr16 + 6735630 6735630 6735630 GCTAAAATAACTTGAAACAGAAGTTGTGTAACATTGGATCGATCACAAAATGTTTGGGTAACAAT GCTAAAATAACTTGAAACAGAAGTTGTGTAACCTTGGATCGATCACAAAATGTTTGGGTAACAAT A C RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1381551512 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12201 17300 RMVar_ID_17300 Human_SNP_ID_592848619 A-to-I Human chr16 + 6757330 6757330 6757330 TATTTACCCAGAGGAAAGAAAATCAATATCTGAAAGGACCTGCACACCCGTGTTTACTGCAGCAT TATTTACCCAGAGGAAAGAAAATCAATATCTGTAAGGACCTGCACACCCGTGTTTACTGCAGCAT A T RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs772306426 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12201 17301 RMVar_ID_17301 Human_SNP_ID_592854658 A-to-I Human chr16 + 6768988 6768988 6768988 TGACCTCGTGATCTGCCTGCCTCGGGCTCCCAAAGTGTTGAGGTTACTGGCGTGAGCCACTGCGC TGACCTCGTGATCTGCCTGCCTCGGGCTCCCAGAGTGTTGAGGTTACTGGCGTGAGCCACTGCGC A G RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1328667215 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12201 17302 RMVar_ID_17302 Human_SNP_ID_592859844 A-to-I Human chr16 + 6779377 6779377 6779377 TGTCATGCTTTTTTGTGGTTGAATAATATTCCATTGTATGTATGTACCACATTTTTTCATTCGGT TGTCATGCTTTTTTGTGGTTGAATAATATTCCGTTGTATGTATGTACCACATTTTTTCATTCGGT A G RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1296049828 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12201 17303 RMVar_ID_17303 Human_SNP_ID_592878720 A-to-I Human chr16 + 6812413 6812413 6812413 TATTTTTTTTGAGACGGAGTCTGGGTCTTGTCACCCAGGCTGGAGTGCAGTGGCCCGATCTCGGC TATTTTTTTTGAGACGGAGTCTGGGTCTTGTCTCCCAGGCTGGAGTGCAGTGGCCCGATCTCGGC A T RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs999426463 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12201 17304 RMVar_ID_17304 Human_SNP_ID_592878854 A-to-I Human chr16 + 6812620 6812620 6812620 ACTGGTCTCAAACTCCTGACCTCAATTGATCCACCCGCCTCAGCCTACCACAGTGCTGGGATTAC ACTGGTCTCAAACTCCTGACCTCAATTGATCCCCCCGCCTCAGCCTACCACAGTGCTGGGATTAC A C RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1027652715 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12201 17305 RMVar_ID_17305 Human_SNP_ID_592881401 A-to-I Human chr16 + 6816884 6816884 6816884 CTCCCACTTCACCCTCCCAAGTAGTTGGGACTAAAGGTAAATACCACCATGCCTAGCTGTTTTTT CTCCCACTTCACCCTCCCAAGTAGTTGGGACTGAAGGTAAATACCACCATGCCTAGCTGTTTTTT A G RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs931890081 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12201 17306 RMVar_ID_17306 Human_SNP_ID_592881469 A-to-I Human chr16 + 6817009 6817009 6817009 TGCTCAAGCGATCCCACTGCCTCTGCCTCCCAAAGTGCTGAGATGGCAGGTGCGAGTCACCATGC TGCTCAAGCGATCCCACTGCCTCTGCCTCCCATAGTGCTGAGATGGCAGGTGCGAGTCACCATGC A T RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1192061233 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12201 17307 RMVar_ID_17307 Human_SNP_ID_592888007 A-to-I Human chr16 + 6828430 6828430 6828430 CCTTTAGACCCAGCTACTCAGGAGACTGAGGCAGGAGAATCACTTGAACCCAGGAGGAAGAGGTT CCTTTAGACCCAGCTACTCAGGAGACTGAGGCCGGAGAATCACTTGAACCCAGGAGGAAGAGGTT A C RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1029490873 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12201 17308 RMVar_ID_17308 Human_SNP_ID_592888008 A-to-I Human chr16 + 6828435 6828435 6828435 AGACCCAGCTACTCAGGAGACTGAGGCAGGAGAATCACTTGAACCCAGGAGGAAGAGGTTGCAGT AGACCCAGCTACTCAGGAGACTGAGGCAGGAGCATCACTTGAACCCAGGAGGAAGAGGTTGCAGT A C RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs777174770 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12201 17309 RMVar_ID_17309 Human_SNP_ID_592891567 A-to-I Human chr16 + 6834948 6834948 6834948 GGTGTCTCGCTCTGTTGCCCAGGCTGGAGTGCAGTGGCGCGATCTTGGTTCACTGTAAGCTTCAT GGTGTCTCGCTCTGTTGCCCAGGCTGGAGTGCGGTGGCGCGATCTTGGTTCACTGTAAGCTTCAT A G RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1361328184 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12201 17310 RMVar_ID_17310 Human_SNP_ID_592892018 A-to-I Human chr16 + 6835719 6835719 6835719 GAGGTTGCAGTGAACCAAGATTGAGTCATTGCACTCCAGCCTGGGTGATAGAGTAAGACTCTGCT GAGGTTGCAGTGAACCAAGATTGAGTCATTGCCCTCCAGCCTGGGTGATAGAGTAAGACTCTGCT A C RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1165838690 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12201 17311 RMVar_ID_17311 Human_SNP_ID_592903967 A-to-I Human chr16 + 6856061 6856061 6856061 AATGGTGCTCATGGTATATGTCTCTCTGGGTTAATGGACCTCAGTGAAGATGAAATGAAGACCCT AATGGTGCTCATGGTATATGTCTCTCTGGGTTGATGGACCTCAGTGAAGATGAAATGAAGACCCT A G RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs919171424 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12201 17312 RMVar_ID_17312 Human_SNP_ID_592920893 A-to-I Human chr16 + 6884702 6884702 6884702 GGTGGATCACTTGAGGCCAGGGGTTCCAGACCAGCTTGGGCAACATGACGAAACCCCATCTGTAC GGTGGATCACTTGAGGCCAGGGGTTCCAGACCGGCTTGGGCAACATGACGAAACCCCATCTGTAC A G RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs552805630 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12201 17313 RMVar_ID_17313 Human_SNP_ID_592920894 A-to-I Human chr16 + 6884702 6884702 6884702 GGTGGATCACTTGAGGCCAGGGGTTCCAGACCAGCTTGGGCAACATGACGAAACCCCATCTGTAC GGTGGATCACTTGAGGCCAGGGGTTCCAGACCTGCTTGGGCAACATGACGAAACCCCATCTGTAC A T RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs552805630 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12201 17314 RMVar_ID_17314 Human_SNP_ID_592920977 A-to-I Human chr16 + 6884839 6884839 6884839 AGAATCTCTTGAACTCAGGAGGTGGAGGTGGCAGTCAGCCCAGAGTGCTCCACTGCACTCCAGCC AGAATCTCTTGAACTCAGGAGGTGGAGGTGGCTGTCAGCCCAGAGTGCTCCACTGCACTCCAGCC A T RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1423168558 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12201 17315 RMVar_ID_17315 Human_SNP_ID_592921487 A-to-I Human chr16 + 6885639 6885639 6885639 CTGCCACCTCTGCCTCCTGAGTTCAAGTGATTATCCTGCCTTAGCCTCCCTAGTAGCTGGGATTA CTGCCACCTCTGCCTCCTGAGTTCAAGTGATTCTCCTGCCTTAGCCTCCCTAGTAGCTGGGATTA A C RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs929177343 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12201 17316 RMVar_ID_17316 Human_SNP_ID_592921488 A-to-I Human chr16 + 6885639 6885639 6885639 CTGCCACCTCTGCCTCCTGAGTTCAAGTGATTATCCTGCCTTAGCCTCCCTAGTAGCTGGGATTA CTGCCACCTCTGCCTCCTGAGTTCAAGTGATTTTCCTGCCTTAGCCTCCCTAGTAGCTGGGATTA A T RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs929177343 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12201 17317 RMVar_ID_17317 Human_SNP_ID_592921531 A-to-I Human chr16 + 6885712 6885712 6885712 TGCCACCACACTCAGCTAATTTTTCTATCTTTAGTAGAGACTGGGTTTCACCAGGTTGGACAGGC TGCCACCACACTCAGCTAATTTTTCTATCTTTTGTAGAGACTGGGTTTCACCAGGTTGGACAGGC A T RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1365623184 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12201 17318 RMVar_ID_17318 Human_SNP_ID_592921562 A-to-I Human chr16 + 6885765 6885765 6885765 GGTTGGACAGGCTGGTCTCGAACTCATGCCTCAGGTGATTCACCTGCCTTGGCCTCCCAAAATGC GGTTGGACAGGCTGGTCTCGAACTCATGCCTCGGGTGATTCACCTGCCTTGGCCTCCCAAAATGC A G RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1401654729 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12201 17319 RMVar_ID_17319 Human_SNP_ID_592921907 A-to-I Human chr16 + 6886315 6886315 6886315 ATCTCTTGACCTCACGTGATCTGCCCACCTCGACCTCCCAAAGTGCTGGGATTACTGGCGTGAGT ATCTCTTGACCTCACGTGATCTGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACTGGCGTGAGT A G RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1255868667 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12201 17320 RMVar_ID_17320 Human_SNP_ID_593033038 A-to-I Human chr16 + 7081235 7081235 7081235 GTTTGTATTTTTAGTGGAGGCAGGGTTTCGCCATGTTGGCTGGGCTGGTCTTGAACTGCTGACCT GTTTGTATTTTTAGTGGAGGCAGGGTTTCGCCTTGTTGGCTGGGCTGGTCTTGAACTGCTGACCT A T RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs554473991 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12201 17321 RMVar_ID_17321 Human_SNP_ID_593039943 A-to-I Human chr16 + 7095418 7095418 7095418 CCTCAGCCTCCCACAGTGCTGGGATTACAGTCATGAGTCACTGCGGCCAGCTTAGAATGTTCTTC CCTCAGCCTCCCACAGTGCTGGGATTACAGTCCTGAGTCACTGCGGCCAGCTTAGAATGTTCTTC A C RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs767052531 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12201 17322 RMVar_ID_17322 Human_SNP_ID_593039944 A-to-I Human chr16 + 7095418 7095418 7095418 CCTCAGCCTCCCACAGTGCTGGGATTACAGTCATGAGTCACTGCGGCCAGCTTAGAATGTTCTTC CCTCAGCCTCCCACAGTGCTGGGATTACAGTCGTGAGTCACTGCGGCCAGCTTAGAATGTTCTTC A G RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs767052531 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12201 17323 RMVar_ID_17323 Human_SNP_ID_593056275 A-to-I Human chr16 + 7129080 7129080 7129080 TAACCTCGTGATCCGCCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACGGCAC TAACCTCGTGATCCGCCCACCTCAGCCTCCCATAGTGCTGGGATTACAGGTGTGAGCCACGGCAC A T RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1190044900 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12201 17324 RMVar_ID_17324 Human_SNP_ID_593057834 A-to-I Human chr16 + 7132146 7132146 7132146 GGAATTACAGGCACCTTCCACCATGCCCAGCTAATTTTTGTATTGTTAATGGAGATGGGGTTTTC GGAATTACAGGCACCTTCCACCATGCCCAGCTGATTTTTGTATTGTTAATGGAGATGGGGTTTTC A G RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1045216820 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12201 17325 RMVar_ID_17325 Human_SNP_ID_593057859 A-to-I Human chr16 + 7132201 7132201 7132201 TGGGGTTTTCCCATGTCAGCCAGGCTGGCCTCAAACTCCTGACTTCGACTGATCTGCCTGTCTCG TGGGGTTTTCCCATGTCAGCCAGGCTGGCCTCGAACTCCTGACTTCGACTGATCTGCCTGTCTCG A G RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1364523921 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12201 17326 RMVar_ID_17326 Human_SNP_ID_593069210 A-to-I Human chr16 + 7155388 7155388 7155388 GAGTTCAGTGGGTCACTTAAGCCAGGAGTTCAAAACCAGCCTGGGATACATGGAAAAACTCCATA GAGTTCAGTGGGTCACTTAAGCCAGGAGTTCACAACCAGCCTGGGATACATGGAAAAACTCCATA A C RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs961371699 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12201 17327 RMVar_ID_17327 Human_SNP_ID_593079197 A-to-I Human chr16 + 7174595 7174595 7174595 TTGAGGTCAGGAGTTTGAGATTAACCTGGTGTAGGTGGTGAAACCCCATCTCTACTAAAAATACA TTGAGGTCAGGAGTTTGAGATTAACCTGGTGTGGGTGGTGAAACCCCATCTCTACTAAAAATACA A G RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1011966020 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12201 17328 RMVar_ID_17328 Human_SNP_ID_593081858 A-to-I Human chr16 + 7179796 7179796 7179796 TTGCTCTGTCACTCAGTCTGGAATGCAGTGGCATGATCTCGGCTCACTGCAACCTACTCCTCCCA TTGCTCTGTCACTCAGTCTGGAATGCAGTGGCGTGATCTCGGCTCACTGCAACCTACTCCTCCCA A G RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1266541832 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12201 17329 RMVar_ID_17329 Human_SNP_ID_593081879 A-to-I Human chr16 + 7179828 7179828 7179828 ATGATCTCGGCTCACTGCAACCTACTCCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTG ATGATCTCGGCTCACTGCAACCTACTCCTCCCTGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTG A T RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1025707477 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12201 17330 RMVar_ID_17330 Human_SNP_ID_593090134 A-to-I Human chr16 + 7194817 7194817 7194817 GGACGTGGTGGTGCATGCCTGTGGTTCTCGCCACTAGGGAGGCTGAGGTGGGAGGATTGCTTAAG GGACGTGGTGGTGCATGCCTGTGGTTCTCGCCGCTAGGGAGGCTGAGGTGGGAGGATTGCTTAAG A G RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1258071421 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12201 17331 RMVar_ID_17331 Human_SNP_ID_593090648 A-to-I Human chr16 + 7195718 7195718 7195718 GGAACTACAGGCCTGCACCACCACACTTGGCTAATTTTTGTATTTTTAGTAGAAACGGGATTTCA GGAACTACAGGCCTGCACCACCACACTTGGCTGATTTTTGTATTTTTAGTAGAAACGGGATTTCA A G RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1037575996 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12201 17332 RMVar_ID_17332 Human_SNP_ID_593165454 A-to-I Human chr16 + 7350102 7350102 7350102 TTGGGAGGCAGAGGTTGCAGTGAGCCGAGATCAGGCCACTGTACTCCAGCTTGGGCGACAGAGCC TTGGGAGGCAGAGGTTGCAGTGAGCCGAGATCGGGCCACTGTACTCCAGCTTGGGCGACAGAGCC A G RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs992479435 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12201 17333 RMVar_ID_17333 Human_SNP_ID_593188704 A-to-I Human chr16 + 7399215 7399215 7399215 CACGCCTGTTATCCCAACATTTTGGGAGGCCGAAGCAGGTGGATTACCTGAGGTCAGTAGTTTGA CACGCCTGTTATCCCAACATTTTGGGAGGCCGGAGCAGGTGGATTACCTGAGGTCAGTAGTTTGA A G RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1166804174 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12201 17334 RMVar_ID_17334 Human_SNP_ID_593672704 A-to-I Human chr16 + 8632415 8632415 8632415 AAATATGGGTCTCACTTTGCACTTCGTTACCCAGGCTGGTCTCAAACTCCTGGCTTCAGGCGATC AAATATGGGTCTCACTTTGCACTTCGTTACCCTGGCTGGTCTCAAACTCCTGGCTTCAGGCGATC A T METTL22 Ensembl:ENSG00000067365 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444251686 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116245,RMVar_hsa_circ_176137,RMVar_hsa_circ_98703,RMVar_hsa_circ_125604,RMVar_hsa_circ_176139,RMVar_hsa_circ_176140,RMVar_hsa_circ_176142,RMVar_hsa_circ_121968 17335 RMVar_ID_17335 Human_SNP_ID_593672991 A-to-I Human chr16 + 8633337 8633337 8633337 GAAGAGCTAGAAAAGGCCGGGCACGGTGGCTCACACCTATGATCCCACTTTGGGAGGCCAAAGCA GAAGAGCTAGAAAAGGCCGGGCACGGTGGCTCCCACCTATGATCCCACTTTGGGAGGCCAAAGCA A C METTL22 Ensembl:ENSG00000067365 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1382548912 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116245,RMVar_hsa_circ_176137,RMVar_hsa_circ_98703,RMVar_hsa_circ_125604,RMVar_hsa_circ_176139,RMVar_hsa_circ_176140,RMVar_hsa_circ_176142,RMVar_hsa_circ_121968 17336 RMVar_ID_17336 Human_SNP_ID_593679152 A-to-I Human chr16 + 8649896 8649896 8649896 TAGTATGCACACGAATCACTTGGGATCTTGTCAAAATACAGATTCTGACTCAGGCCCTGGATGTG TAGTATGCACACGAATCACTTGGGATCTTGTCCAAATACAGATTCTGACTCAGGCCCTGGATGTG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1301629877 Functional Loss SNV dbSNP153 33..33 33 - - - 17337 RMVar_ID_17337 Human_SNP_ID_593679154 A-to-I Human chr16 + 8649901 8649901 8649901 TGCACACGAATCACTTGGGATCTTGTCAAAATACAGATTCTGACTCAGGCCCTGGATGTGGCCTG TGCACACGAATCACTTGGGATCTTGTCAAAATGCAGATTCTGACTCAGGCCCTGGATGTGGCCTG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1440096903 Functional Loss SNV dbSNP153 33..33 33 - - - 17338 RMVar_ID_17338 Human_SNP_ID_593707740 A-to-I Human chr16 + 8737334 8737334 8737334 CCCCGTCTCTACCAAAAATACAAAAATTAGCCAGGTATGGTGGTGGATGCCTGTAATCCCAACTA CCCCGTCTCTACCAAAAATACAAAAATTAGCCCGGTATGGTGGTGGATGCCTGTAATCCCAACTA A C ABAT Ensembl:ENSG00000183044 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1344408438 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_176150,RMVar_hsa_circ_176148,RMVar_hsa_circ_93387,RMVar_hsa_circ_287182,RMVar_hsa_circ_325217,RMVar_hsa_circ_14906,RMVar_hsa_circ_176149 17339 RMVar_ID_17339 Human_SNP_ID_593723855 A-to-I Human chr16 - 8783977 8783977 8783977 GAAATTCTTCTAGCTAAAGCCCCAGCCCCCAAAAGAGCATGTCTCAGGAACTCATTATGCCCTGA GAAATTCTTCTAGCTAAAGCCCCAGCCCCCAAGAGAGCATGTCTCAGGAACTCATTATGCCCTGA T C TMEM186 Ensembl:ENSG00000184857 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1003591619 Functional Loss SNV dbSNP153 33..33 33 - - - 17340 RMVar_ID_17340 Human_SNP_ID_593723856 A-to-I Human chr16 - 8783977 8783977 8783977 GAAATTCTTCTAGCTAAAGCCCCAGCCCCCAAAAGAGCATGTCTCAGGAACTCATTATGCCCTGA GAAATTCTTCTAGCTAAAGCCCCAGCCCCCAACAGAGCATGTCTCAGGAACTCATTATGCCCTGA T G TMEM186 Ensembl:ENSG00000184857 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1003591619 Functional Loss SNV dbSNP153 33..33 33 - - - 17341 RMVar_ID_17341 Human_SNP_ID_593729151 A-to-I Human chr16 + 8800175 8800175 8800175 GAGGTCAGGAGTTCGAGACCAGCCTTGCCAACATGGTGAAACCCAGTCTCTACTAAAAATACAAA GAGGTCAGGAGTTCGAGACCAGCCTTGCCAACGTGGTGAAACCCAGTCTCTACTAAAAATACAAA A G PMM2 Ensembl:ENSG00000140650 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs141088386 Functional Loss SNV dbSNP153 33..33 33 - - - 17342 RMVar_ID_17342 Human_SNP_ID_593729152 A-to-I Human chr16 + 8800175 8800175 8800175 GAGGTCAGGAGTTCGAGACCAGCCTTGCCAACATGGTGAAACCCAGTCTCTACTAAAAATACAAA GAGGTCAGGAGTTCGAGACCAGCCTTGCCAACTTGGTGAAACCCAGTCTCTACTAAAAATACAAA A T PMM2 Ensembl:ENSG00000140650 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs141088386 Functional Loss SNV dbSNP153 33..33 33 - - - 17343 RMVar_ID_17343 Human_SNP_ID_593729176 A-to-I Human chr16 + 8800240 8800240 8800240 AAGATTAGCCGAGCATGATGGCGGGCGCCTGTAATCCTGGCTACCTGGGAGGCTGAGACAGGAGA AAGATTAGCCGAGCATGATGGCGGGCGCCTGTTATCCTGGCTACCTGGGAGGCTGAGACAGGAGA A T PMM2 Ensembl:ENSG00000140650 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1047943825 Functional Loss SNV dbSNP153 33..33 33 - - - 17344 RMVar_ID_17344 Human_SNP_ID_593729652 A-to-I Human chr16 + 8801548 8801548 8801548 AAAAAATTAGCCAGGTGTGCTGGCACATAACTATGGTCCCAGCTACTCAGGAGGCAGAGATAGGA AAAAAATTAGCCAGGTGTGCTGGCACATAACTGTGGTCCCAGCTACTCAGGAGGCAGAGATAGGA A G PMM2 Ensembl:ENSG00000140650 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1024523452 Functional Loss SNV dbSNP153 33..33 33 - - - 17345 RMVar_ID_17345 Human_SNP_ID_593732066 A-to-I Human chr16 + 8808554 8808553 8808554 ATTTGCCTGACAACACTAACTACATGCCCCACAACGGCCAGGCAGATGCAGTAAGACTTCAGAGA ATTTGCCTGACAACACTAACTACATGCCCCAGGACGGCCAGGCAGATGCAGTAAGACTTCAGAGA CA GG PMM2 Ensembl:ENSG00000140650 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs386788720 Functional Loss MNV dbSNP153 32..33 33 - - - RMVar_hsa_circ_1085,RMVar_hsa_circ_353625,RMVar_hsa_circ_62317,RMVar_hsa_circ_278480,RMVar_hsa_circ_176161 17346 RMVar_ID_17346 Human_SNP_ID_593732069 A-to-I Human chr16 + 8808554 8808554 8808554 ATTTGCCTGACAACACTAACTACATGCCCCACAACGGCCAGGCAGATGCAGTAAGACTTCAGAGA ATTTGCCTGACAACACTAACTACATGCCCCACGACGGCCAGGCAGATGCAGTAAGACTTCAGAGA A G PMM2 Ensembl:ENSG00000140650 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4985037 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_1239,GWAS_ID_1240,GWAS_ID_1241 RMVar_hsa_circ_1085,RMVar_hsa_circ_353625,RMVar_hsa_circ_62317,RMVar_hsa_circ_278480,RMVar_hsa_circ_176161 17347 RMVar_ID_17347 Human_SNP_ID_593732070 A-to-I Human chr16 + 8808554 8808554 8808556 ATTTGCCTGACAACACTAACTACATGCCCCACAACGGCCAGGCAGATGCAGTAAGACTTCAGAGA ATTTGCCTGACAACACTAACTACATGCCCCACGATGGCCAGGCAGATGCAGTAAGACTTCAGAGA AAC GAT PMM2 Ensembl:ENSG00000140650 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs796715814 Functional Loss MNV dbSNP153 33..35 33 - - - RMVar_hsa_circ_1085,RMVar_hsa_circ_353625,RMVar_hsa_circ_62317,RMVar_hsa_circ_278480,RMVar_hsa_circ_176161 17348 RMVar_ID_17348 Human_SNP_ID_593734760 A-to-I Human chr16 + 8817217 8817217 8817217 AGGAGGTGTAGCATTCAGGTTTGTTCTTAATGACAGTTACATATGGTTTTATAACCACATCCTTT AGGAGGTGTAGCATTCAGGTTTGTTCTTAATGGCAGTTACATATGGTTTTATAACCACATCCTTT A G PMM2 Ensembl:ENSG00000140650 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1529913 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_1242,GWAS_ID_1243 17349 RMVar_ID_17349 Human_SNP_ID_593734761 A-to-I Human chr16 + 8817217 8817217 8817217 AGGAGGTGTAGCATTCAGGTTTGTTCTTAATGACAGTTACATATGGTTTTATAACCACATCCTTT AGGAGGTGTAGCATTCAGGTTTGTTCTTAATGTCAGTTACATATGGTTTTATAACCACATCCTTT A T PMM2 Ensembl:ENSG00000140650 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1529913 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_1242,GWAS_ID_1243 17350 RMVar_ID_17350 Human_SNP_ID_593735750 A-to-I Human chr16 + 8820417 8820417 8820417 ACTCTGTCACCCAGACTGGAGTGCAGTGGCGCAATCTTGGTTCACTGTAATCTTGAACTCCTGGG ACTCTGTCACCCAGACTGGAGTGCAGTGGCGCGATCTTGGTTCACTGTAATCTTGAACTCCTGGG A G PMM2 Ensembl:ENSG00000140650 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1463655606 Functional Loss SNV dbSNP153 33..33 33 - - - 17351 RMVar_ID_17351 Human_SNP_ID_593747555 A-to-I Human chr16 + 8851479 8851479 8851479 CCAAAGTGCTGAAATTACAGGCGTGAGCTACCACGCCCGCTCCCCACCTTCAGCTTTTGCCAAAC CCAAAGTGCTGAAATTACAGGCGTGAGCTACCGCGCCCGCTCCCCACCTTCAGCTTTTGCCAAAC A G AC022167.2 Ensembl:ENSG00000260276 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054047315 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18687309 17352 RMVar_ID_17352 Human_SNP_ID_593747931 A-to-I Human chr16 + 8852216 8852216 8852216 TGATGCCCAGCTGGTCTCAAACCCCTGAGCTCAAGCCATCCACCTACCTCGGCCTCTCAAAATGC TGATGCCCAGCTGGTCTCAAACCCCTGAGCTCCAGCCATCCACCTACCTCGGCCTCTCAAAATGC A C AC022167.2 Ensembl:ENSG00000260276 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs564266985 Functional Loss SNV dbSNP153 33..33 33 - - - 17353 RMVar_ID_17353 Human_SNP_ID_593747932 A-to-I Human chr16 + 8852216 8852216 8852216 TGATGCCCAGCTGGTCTCAAACCCCTGAGCTCAAGCCATCCACCTACCTCGGCCTCTCAAAATGC TGATGCCCAGCTGGTCTCAAACCCCTGAGCTCGAGCCATCCACCTACCTCGGCCTCTCAAAATGC A G AC022167.2 Ensembl:ENSG00000260276 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs564266985 Functional Loss SNV dbSNP153 33..33 33 - - - 17354 RMVar_ID_17354 Human_SNP_ID_593748053 A-to-I Human chr16 + 8852506 8852506 8852506 GTCCCAGCTACTCAGGTGGCTGAAGGAGGATCACTTGAGCCCACAAGGTTAAGGCTGCAGGGCAA GTCCCAGCTACTCAGGTGGCTGAAGGAGGATCCCTTGAGCCCACAAGGTTAAGGCTGCAGGGCAA A C AC022167.2 Ensembl:ENSG00000260276 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs986915063 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17563939 17355 RMVar_ID_17355 Human_SNP_ID_593748054 A-to-I Human chr16 + 8852506 8852506 8852506 GTCCCAGCTACTCAGGTGGCTGAAGGAGGATCACTTGAGCCCACAAGGTTAAGGCTGCAGGGCAA GTCCCAGCTACTCAGGTGGCTGAAGGAGGATCTCTTGAGCCCACAAGGTTAAGGCTGCAGGGCAA A T AC022167.2 Ensembl:ENSG00000260276 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs986915063 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17563939 17356 RMVar_ID_17356 Human_SNP_ID_593748727 A-to-I Human chr16 - 8853869 8853869 8853869 GTTGGGCAGGATGGTCTTGAACCCCTGACCTCAGATGATCTGCCCATCTCGGCCTCTCAAAGTGC GTTGGGCAGGATGGTCTTGAACCCCTGACCTCGGATGATCTGCCCATCTCGGCCTCTCAAAGTGC T C CARHSP1 Ensembl:ENSG00000153048 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs764882927 Functional Loss SNV dbSNP153 33..33 33 - - - 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 17357 RMVar_ID_17357 Human_SNP_ID_593748739 A-to-I Human chr16 + 8853905 8853905 8853905 GTCAGGGGTTCAAGACCATCCTGCCCAACATGATGAAACCTGGTCTCTACTAAAAATACAAAAAT GTCAGGGGTTCAAGACCATCCTGCCCAACATGGTGAAACCTGGTCTCTACTAAAAATACAAAAAT A G AC022167.1,AC022167.2 Ensembl:ENSG00000259939,Ensembl:ENSG00000260276 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006375292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3509939 17358 RMVar_ID_17358 Human_SNP_ID_593748741 A-to-I Human chr16 - 8853920 8853920 8853920 CACCACACCCGGTTAATTTTTGTATTTTTAGTAGAGACCAGGTTTCATCATGTTGGGCAGGATGG CACCACACCCGGTTAATTTTTGTATTTTTAGTGGAGACCAGGTTTCATCATGTTGGGCAGGATGG T C CARHSP1 Ensembl:ENSG00000153048 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1469110374 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2490399,Human_RBP_ID_12851517 Human_miRNA_ID_2724105,Human_miRNA_ID_2724106 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 17359 RMVar_ID_17359 Human_SNP_ID_593748766 A-to-I Human chr16 + 8853965 8853965 8853965 AAAATTAACCGGGTGTGGTGGCGCATGCCTGTAATCCCAGCTACTCAGGAGACTGAGGCGGAATT AAAATTAACCGGGTGTGGTGGCGCATGCCTGTGATCCCAGCTACTCAGGAGACTGAGGCGGAATT A G AC022167.1,AC022167.2 Ensembl:ENSG00000259939,Ensembl:ENSG00000260276 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1469002485 Functional Loss SNV dbSNP153 33..33 33 - - - 17360 RMVar_ID_17360 Human_SNP_ID_593748803 A-to-I Human chr16 - 8854037 8854034 8854038 TTCTGTCACCCAGGCTGGAGTGCAGTGGCCCGATCTCAGCTTACTGCAACCTCTGCCCTCCAGGG TTCTGTCACCCAGGCTGGAGTGCAGTGGCCC____TCAGCTTACTGCAACCTCTGCCCTCCAGGG AGATC A CARHSP1 Ensembl:ENSG00000153048 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1036430305 Functional Loss DEL dbSNP153 32..35 33 - - - 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 17361 RMVar_ID_17361 Human_SNP_ID_593749801 A-to-I Human chr16 + 8855892 8855892 8855892 TTGCCCAGGCTGGAGTGCAGTGGTGTGATCTCAGCTTACTGCATCCACCTCCCGAGTTCAAGTGA TTGCCCAGGCTGGAGTGCAGTGGTGTGATCTCCGCTTACTGCATCCACCTCCCGAGTTCAAGTGA A C AC022167.2 Ensembl:ENSG00000260276 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs557620699 Functional Loss SNV dbSNP153 33..33 33 - - - 17362 RMVar_ID_17362 Human_SNP_ID_593752435 A-to-I Human chr16 + 8859879 8859879 8859879 AGGCACCTGTAATCCCATCTACTTGAAGGCTGAGGCATGAGAATTGCTTGAACCTGGGAGGCGGA AGGCACCTGTAATCCCATCTACTTGAAGGCTGCGGCATGAGAATTGCTTGAACCTGGGAGGCGGA A C AC022167.2 Ensembl:ENSG00000260276 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs906948891 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_3193557 17363 RMVar_ID_17363 Human_SNP_ID_593752436 A-to-I Human chr16 + 8859879 8859879 8859879 AGGCACCTGTAATCCCATCTACTTGAAGGCTGAGGCATGAGAATTGCTTGAACCTGGGAGGCGGA AGGCACCTGTAATCCCATCTACTTGAAGGCTGGGGCATGAGAATTGCTTGAACCTGGGAGGCGGA A G AC022167.2 Ensembl:ENSG00000260276 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs906948891 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_3193557 17364 RMVar_ID_17364 Human_SNP_ID_593753239 A-to-I Human chr16 + 8861266 8861266 8861266 ATCTCAAACTCCTGGGCTCAACGGATTCTCCCACCTCTTCCTCTCAAAGTGCTAGGATTACAGGC ATCTCAAACTCCTGGGCTCAACGGATTCTCCCGCCTCTTCCTCTCAAAGTGCTAGGATTACAGGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232642188 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6547314,Human_RBP_ID_12854879 17365 RMVar_ID_17365 Human_SNP_ID_593765203 A-to-I Human chr16 - 8893160 8893160 8893160 TTAGCAAGAGGGCATGCTCACTAGTGGTTAGTAAGCTGTCGACTTTGTAAAAAAGTTAAAAATGA TTAGCAAGAGGGCATGCTCACTAGTGGTTAGTCAGCTGTCGACTTTGTAAAAAAGTTAAAAATGA T G USP7 Ensembl:ENSG00000187555 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1229651324 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_482268,Human_RBP_ID_2491093,Human_RBP_ID_9840544,Human_RBP_ID_12860689,Human_RBP_ID_23707850 Human_miRNA_ID_575218,Human_miRNA_ID_1333846 17366 RMVar_ID_17366 Human_SNP_ID_593772911 A-to-I Human chr16 - 8913937 8913937 8913937 ACCCAGGAGTTTGAGGCCAGCCTGGGCAACATAGTGAGACTCCATCTCTACAAATTAGCTGGGCG ACCCAGGAGTTTGAGGCCAGCCTGGGCAACATGGTGAGACTCCATCTCTACAAATTAGCTGGGCG T C USP7 Ensembl:ENSG00000187555 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1165543477 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47537,RMVar_hsa_circ_4879,RMVar_hsa_circ_71810,RMVar_hsa_circ_275924,RMVar_hsa_circ_19243,RMVar_hsa_circ_58323,RMVar_hsa_circ_176177,RMVar_hsa_circ_36963,RMVar_hsa_circ_322804,RMVar_hsa_circ_363259,RMVar_hsa_circ_176178,RMVar_hsa_circ_271704,RMVar_hsa_circ_176179 17367 RMVar_ID_17367 Human_SNP_ID_593774494 A-to-I Human chr16 - 8918647 8918647 8918647 CCGCCACCACGGCCAGCTAATTTTTATATTTTAGTAGAGGCGGGGTTTCACCATGTTGTCCAGGC CCGCCACCACGGCCAGCTAATTTTTATATTTTGGTAGAGGCGGGGTTTCACCATGTTGTCCAGGC T C USP7 Ensembl:ENSG00000187555 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1289122686 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47537,RMVar_hsa_circ_71810,RMVar_hsa_circ_363259,RMVar_hsa_circ_346168,RMVar_hsa_circ_317861,RMVar_hsa_circ_296104,RMVar_hsa_circ_176182,RMVar_hsa_circ_176181,RMVar_hsa_circ_341725 17368 RMVar_ID_17368 Human_SNP_ID_593779822 A-to-I Human chr16 - 8933362 8933362 8933362 TTTGTTTTTAATAGAGTTGGGAATCTCACTATATTGCCCATGTTGGTCTCGGACTCCTTGACTTA TTTGTTTTTAATAGAGTTGGGAATCTCACTATGTTGCCCATGTTGGTCTCGGACTCCTTGACTTA T C USP7 Ensembl:ENSG00000187555 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs890791928 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12865196 17369 RMVar_ID_17369 Human_SNP_ID_593839367 A-to-I Human chr16 + 9104201 9104201 9104201 CATTGGCGCGATATTGGCTCACCGCGACCTCTACCTCTGGGTTCAAGCGATTCTCCTGCCTCAGC CATTGGCGCGATATTGGCTCACCGCGACCTCTCCCTCTGGGTTCAAGCGATTCTCCTGCCTCAGC A C C16orf72 Ensembl:ENSG00000182831 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs371033090 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_482488,Human_RBP_ID_6549024,Human_RBP_ID_12866155 17370 RMVar_ID_17370 Human_SNP_ID_593839368 A-to-I Human chr16 + 9104201 9104201 9104201 CATTGGCGCGATATTGGCTCACCGCGACCTCTACCTCTGGGTTCAAGCGATTCTCCTGCCTCAGC CATTGGCGCGATATTGGCTCACCGCGACCTCTGCCTCTGGGTTCAAGCGATTCTCCTGCCTCAGC A G C16orf72 Ensembl:ENSG00000182831 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs371033090 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_482488,Human_RBP_ID_6549024,Human_RBP_ID_12866155 17371 RMVar_ID_17371 Human_SNP_ID_593839408 A-to-I Human chr16 + 9104292 9104292 9104292 TGTGCCACCACGCCGGCTAATTTTTTAGAGACAGGGTTTCACCGTGTTGGTCAGGCTGGTCTCGA TGTGCCACCACGCCGGCTAATTTTTTAGAGACGGGGTTTCACCGTGTTGGTCAGGCTGGTCTCGA A G C16orf72 Ensembl:ENSG00000182831 Protein coding intron GSE100210;GSE99789;GSE107867;GSE107867;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,EC109;ASD brains,Fragile X samples from NIH NeuroBioBank;ASD brains,frontal_cortex;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,29796672,30559470,30559470,32596459 RNA-Seq:(High) rs1032789705 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_482490,Human_RBP_ID_6549029,Human_RBP_ID_12866161 17372 RMVar_ID_17372 Human_SNP_ID_593840083 A-to-I Human chr16 + 9106354 9106354 9106354 CGCTCTATAGCCCAGGCTGGAGTGTAGTGCTCACTGCGACTTCCGCCTCCTGGGTTCAAATGATT CGCTCTATAGCCCAGGCTGGAGTGTAGTGCTCCCTGCGACTTCCGCCTCCTGGGTTCAAATGATT A C C16orf72,AC087190.3 Ensembl:ENSG00000182831,Ensembl:ENSG00000263244 Protein coding,lincRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1359745790 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_762532,Human_RBP_ID_816745,Human_RBP_ID_5247691,Human_RBP_ID_5259634,Human_RBP_ID_6549112,Human_RBP_ID_12866288,Human_RBP_ID_18288411,Human_RBP_ID_20166405,Human_RBP_ID_23708486 17373 RMVar_ID_17373 Human_SNP_ID_593840119 A-to-I Human chr16 + 9106454 9106454 9106454 GGCGCCTGCCACCACGCCCAGCTAATTTTTGTATTTGTAGTAGAGATGGGGTTTCATCATGTTGG GGCGCCTGCCACCACGCCCAGCTAATTTTTGTGTTTGTAGTAGAGATGGGGTTTCATCATGTTGG A G C16orf72,AC087190.3 Ensembl:ENSG00000182831,Ensembl:ENSG00000263244 Protein coding,lincRNA intron,exon GSE47997;GSE38233;GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,29129909,32596459 RNA-Seq:(High) rs976931235 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_482554,Human_RBP_ID_12866298,Human_RBP_ID_20166407,Human_RBP_ID_26444535 17374 RMVar_ID_17374 Human_SNP_ID_593840120 A-to-I Human chr16 + 9106460 9106460 9106460 TGCCACCACGCCCAGCTAATTTTTGTATTTGTAGTAGAGATGGGGTTTCATCATGTTGGCGAAGC TGCCACCACGCCCAGCTAATTTTTGTATTTGTGGTAGAGATGGGGTTTCATCATGTTGGCGAAGC A G C16orf72,AC087190.3 Ensembl:ENSG00000182831,Ensembl:ENSG00000263244 Protein coding,lincRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs563159180 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_482554,Human_RBP_ID_4392441,Human_RBP_ID_6552399,Human_RBP_ID_12882557,Human_RBP_ID_26444535 17375 RMVar_ID_17375 Human_SNP_ID_593840141 A-to-I Human chr16 + 9106489 9106489 9106489 TGTAGTAGAGATGGGGTTTCATCATGTTGGCGAAGCTGGTCTTGAACACCTGACCTCAAGTGATC TGTAGTAGAGATGGGGTTTCATCATGTTGGCGGAGCTGGTCTTGAACACCTGACCTCAAGTGATC A G C16orf72,AC087190.3 Ensembl:ENSG00000182831,Ensembl:ENSG00000263244 Protein coding,lincRNA intron,exon GSE107867;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 ASD brains,temporal_cortex;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 30559470,32596459,32596459 RNA-Seq:(High) rs1347119695 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_482554,Human_RBP_ID_762533,Human_RBP_ID_3510326,Human_RBP_ID_6549115,Human_RBP_ID_8188902,Human_RBP_ID_12866300,Human_RBP_ID_26444538 17376 RMVar_ID_17376 Human_SNP_ID_593840159 A-to-I Human chr16 + 9106547 9106547 9106547 AGTGATCTGCCTTAGCCTCACTGCTTGCCCCTAAGTGGTGGGATTGCAGGTGTGAGCCACTGTGC AGTGATCTGCCTTAGCCTCACTGCTTGCCCCTGAGTGGTGGGATTGCAGGTGTGAGCCACTGTGC A G C16orf72,AC087190.3 Ensembl:ENSG00000182831,Ensembl:ENSG00000263244 Protein coding,lincRNA intron,exon GSE100210;GSE107867 HepG2 cell line;ASD brains,temporal_cortex - 29129909,30559470 RNA-Seq:(High) rs1236529886 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_482555,Human_RBP_ID_5259635,Human_RBP_ID_5648269,Human_RBP_ID_6549117,Human_RBP_ID_17563941,Human_RBP_ID_26444859 17377 RMVar_ID_17377 Human_SNP_ID_593841573 A-to-I Human chr16 + 9110818 9110818 9110818 CCAGCACTTTGGGAGGCCAAGGCGGGTGAATCACCTGAGGTCAGGAGTTTGAGACCGGCCTGACC CCAGCACTTTGGGAGGCCAAGGCGGGTGAATCGCCTGAGGTCAGGAGTTTGAGACCGGCCTGACC A G C16orf72,AC087190.3 Ensembl:ENSG00000182831,Ensembl:ENSG00000263244 Protein coding,lincRNA intron,exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1195810825 Functional Loss SNV dbSNP153 33..33 33 - - - 17378 RMVar_ID_17378 Human_SNP_ID_593841599 A-to-I Human chr16 + 9110882 9110882 9110882 CAACTTGGAGAAACCCCGTCTCTACTAAAAATACAAAAATTAGTCAGGGGTGGTGGCGCATGCCT CAACTTGGAGAAACCCCGTCTCTACTAAAAATGCAAAAATTAGTCAGGGGTGGTGGCGCATGCCT A G C16orf72,AC087190.3 Ensembl:ENSG00000182831,Ensembl:ENSG00000263244 Protein coding,lincRNA intron,exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1394233391 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3510335,Human_RBP_ID_5097205,Human_RBP_ID_12866638 17379 RMVar_ID_17379 Human_SNP_ID_593841617 A-to-I Human chr16 + 9110917 9110917 9110917 AAAATTAGTCAGGGGTGGTGGCGCATGCCTGTAATCCTGTCTACTCAGGAGGCTGAGGCAGGAGA AAAATTAGTCAGGGGTGGTGGCGCATGCCTGTGATCCTGTCTACTCAGGAGGCTGAGGCAGGAGA A G C16orf72,AC087190.3 Ensembl:ENSG00000182831,Ensembl:ENSG00000263244 Protein coding,lincRNA intron,exon GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1038804130 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3510335,Human_RBP_ID_4392561,Human_RBP_ID_5097205,Human_RBP_ID_8188546,Human_RBP_ID_25240123 17380 RMVar_ID_17380 Human_SNP_ID_593841623 A-to-I Human chr16 + 9110931 9110931 9110931 GTGGTGGCGCATGCCTGTAATCCTGTCTACTCAGGAGGCTGAGGCAGGAGAATTGCCTGAACCCG GTGGTGGCGCATGCCTGTAATCCTGTCTACTCCGGAGGCTGAGGCAGGAGAATTGCCTGAACCCG A C C16orf72,AC087190.3 Ensembl:ENSG00000182831,Ensembl:ENSG00000263244 Protein coding,lincRNA intron,exon GSE38233;GSE100210;GSE99789;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;ASD brains,Fragile X samples from NIH NeuroBioBank;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,29796672,30559470,31158229,31158229,31158229 RNA-Seq:(High) rs1000979867 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3510335,Human_RBP_ID_5097205,Human_RBP_ID_8188546 17381 RMVar_ID_17381 Human_SNP_ID_593841624 A-to-I Human chr16 + 9110931 9110931 9110931 GTGGTGGCGCATGCCTGTAATCCTGTCTACTCAGGAGGCTGAGGCAGGAGAATTGCCTGAACCCG GTGGTGGCGCATGCCTGTAATCCTGTCTACTCGGGAGGCTGAGGCAGGAGAATTGCCTGAACCCG A G C16orf72,AC087190.3 Ensembl:ENSG00000182831,Ensembl:ENSG00000263244 Protein coding,lincRNA intron,exon GSE38233;GSE100210;GSE99789;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;ASD brains,Fragile X samples from NIH NeuroBioBank;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,29796672,30559470,31158229,31158229,31158229 RNA-Seq:(High) rs1000979867 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3510335,Human_RBP_ID_5097205,Human_RBP_ID_8188546 17382 RMVar_ID_17382 Human_SNP_ID_593841651 A-to-I Human chr16 + 9110990 9110990 9110990 AACCCGGGAGGCAGAGGTTGCAGTGAGCTGAGATCGTGCCATTGCACTCCAGCCTGGGCAACAAG AACCCGGGAGGCAGAGGTTGCAGTGAGCTGAGTTCGTGCCATTGCACTCCAGCCTGGGCAACAAG A T C16orf72,AC087190.3 Ensembl:ENSG00000182831,Ensembl:ENSG00000263244 Protein coding,lincRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1397105745 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4392564 17383 RMVar_ID_17383 Human_SNP_ID_593841663 A-to-I Human chr16 + 9111026 9111026 9111026 TGCCATTGCACTCCAGCCTGGGCAACAAGAGCAAAACTCAGTCTCAAAAAACAAAACAAAAACCT TGCCATTGCACTCCAGCCTGGGCAACAAGAGCCAAACTCAGTCTCAAAAAACAAAACAAAAACCT A C C16orf72,AC087190.3 Ensembl:ENSG00000182831,Ensembl:ENSG00000263244 Protein coding,lincRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1195219200 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8084282,Human_RBP_ID_17255767,Human_RBP_ID_17371172,Human_RBP_ID_17488142 17384 RMVar_ID_17384 Human_SNP_ID_593843911 A-to-I Human chr16 + 9118473 9118473 9118473 TCATTGACTGGGTGGGATGTGAATGGAATGTTAGAAATGTTGTGTGAATTGAAGTTCTGTATTCA TCATTGACTGGGTGGGATGTGAATGGAATGTTGGAAATGTTGTGTGAATTGAAGTTCTGTATTCA A G C16orf72 Ensembl:ENSG00000182831 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs183903688 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_482660,Human_RBP_ID_1526879,Human_RBP_ID_1848394,Human_RBP_ID_2491469,Human_RBP_ID_3502107,Human_RBP_ID_4392622,Human_RBP_ID_23708586 Human_miRNA_ID_1773901 17385 RMVar_ID_17385 Human_SNP_ID_593848057 A-to-I Human chr16 + 9130296 9130293 9130297 GCAGTAACACAATCATAACTCACTGCAGCCTCAGACTCCCAGGCTTAAGCAATCCTCCCACCTCA GCAGTAACACAATCATAACTCACTGCAGCC____ACTCCCAGGCTTAAGCAATCCTCCCACCTCA CTCAG C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1411630481 Functional Loss DEL dbSNP153 31..34 33 - - - 17386 RMVar_ID_17386 Human_SNP_ID_593848359 A-to-I Human chr16 + 9131255 9131255 9131255 GTGGCTCACTGCAGCCTCAACCTCCCAGGCCCAATTGATCTTCCAGCCTCAGCTTTCCAAGTAGT GTGGCTCACTGCAGCCTCAACCTCCCAGGCCCGATTGATCTTCCAGCCTCAGCTTTCCAAGTAGT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1156968433 Functional Loss SNV dbSNP153 33..33 33 - - - 17387 RMVar_ID_17387 Human_SNP_ID_593848965 A-to-I Human chr16 + 9132717 9132716 9132717 AAAATTAGTTGGGCCCAGTGGCGTGTGCCTGTAATCCCAGCTACTCAGGTGGCTGAGGCATGAGA AAAATTAGTTGGGCCCAGTGGCGTGTGCCTGT_ATCCCAGCTACTCAGGTGGCTGAGGCATGAGA TA T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1354227135 Functional Loss DEL dbSNP153 33..33 33 - - - 17388 RMVar_ID_17388 Human_SNP_ID_593851743 A-to-I Human chr16 + 9140438 9140438 9140438 CACTCTTGTCACCCAGGGTGGAGTCCAATGGTACGATCTTGGCTCACTGCAACCTCCACCTCCCG CACTCTTGTCACCCAGGGTGGAGTCCAATGGTGCGATCTTGGCTCACTGCAACCTCCACCTCCCG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1320710060 Functional Loss SNV dbSNP153 33..33 33 - - - 17389 RMVar_ID_17389 Human_SNP_ID_593851784 A-to-I Human chr16 + 9140552 9140552 9140552 ATGCATCCCACCACGCCTGGCTGGTTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTGGG ATGCATCCCACCACGCCTGGCTGGTTTTTTGTCTTTTTAGTAGAGACGGGGTTTCACCATGTGGG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs969130326 Functional Loss SNV dbSNP153 33..33 33 - - - 17390 RMVar_ID_17390 Human_SNP_ID_593854296 A-to-I Human chr16 + 9148239 9148239 9148239 GCACCACTGCACTCCAGCCTGGGCGACAGAGCAAGACTCTGTGTCAAAGAAAAAAAAAAAAAAAG GCACCACTGCACTCCAGCCTGGGCGACAGAGCGAGACTCTGTGTCAAAGAAAAAAAAAAAAAAAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1188804865 Functional Loss SNV dbSNP153 33..33 33 - - - 17391 RMVar_ID_17391 Human_SNP_ID_593855440 A-to-I Human chr16 + 9151647 9151647 9151647 GTGCCTCCGCGCCTGGCTAATTTATTTTTTGTAGAGATGGGCTGTCACCATGTTGGCCAGGCTGG GTGCCTCCGCGCCTGGCTAATTTATTTTTTGTGGAGATGGGCTGTCACCATGTTGGCCAGGCTGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1181961239 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12867628 RMVar_hsa_circ_176190 17392 RMVar_ID_17392 Human_SNP_ID_594139068 A-to-I Human chr16 - 10065890 10065890 10065890 ACCCATGTTTCCACCCAGTATCTATCACCCTGAGACCGTGGGAGGAATGACCAAACCATGTTAAG ACCCATGTTTCCACCCAGTATCTATCACCCTGTGACCGTGGGAGGAATGACCAAACCATGTTAAG T A GRIN2A Ensembl:ENSG00000183454 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1399421070 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16916 17393 RMVar_ID_17393 Human_SNP_ID_594139300 A-to-I Human chr16 - 10066645 10066645 10066645 GGCAGCTTAAGATGCTTCAGTCACTCATCCTAAGGTCTCAGAGTGATAGATCCTGGGTGGAAACA GGCAGCTTAAGATGCTTCAGTCACTCATCCTACGGTCTCAGAGTGATAGATCCTGGGTGGAAACA T G GRIN2A Ensembl:ENSG00000183454 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1054437698 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5259028 RMVar_hsa_circ_16916 17394 RMVar_ID_17394 Human_SNP_ID_594141373 A-to-I Human chr16 - 10073159 10073159 10073159 TTGAGGTCAGGAGTTTGAGACCAGCTTGGCCAACATGGTGAAACCCCATCTCTACTAACAATACA TTGAGGTCAGGAGTTTGAGACCAGCTTGGCCAGCATGGTGAAACCCCATCTCTACTAACAATACA T C GRIN2A Ensembl:ENSG00000183454 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1234390907 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16916 17395 RMVar_ID_17395 Human_SNP_ID_594162555 A-to-I Human chr16 - 10139965 10139965 10139965 ATTTCTCATTTACTGGATCTCAGGTGCCTGTAATCCCAGCTACTCTGGAGACTGAGGCATGAGGA ATTTCTCATTTACTGGATCTCAGGTGCCTGTAGTCCCAGCTACTCTGGAGACTGAGGCATGAGGA T C GRIN2A Ensembl:ENSG00000183454 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1302092158 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16916 17396 RMVar_ID_17396 Human_SNP_ID_594168599 A-to-I Human chr16 - 10161081 10161081 10161081 CCCTCCCACAACACGTGAGGATGATGGGAACTACAATTCAAGATGAGATTTATGTGGGGACACAG CCCTCCCACAACACGTGAGGATGATGGGAACTGCAATTCAAGATGAGATTTATGTGGGGACACAG T C GRIN2A Ensembl:ENSG00000183454 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1047093143 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16916 17397 RMVar_ID_17397 Human_SNP_ID_594247324 A-to-I Human chr16 + 10397619 10397619 10397619 AGAAAATGGGCTGGGCGTGGTGGCTCATGCCTACAATCCCAGGACTTTGGGAGGCCAAAGCGGGT AGAAAATGGGCTGGGCGTGGTGGCTCATGCCTGCAATCCCAGGACTTTGGGAGGCCAAAGCGGGT A G ATF7IP2 Ensembl:ENSG00000166669 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs530173374 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25189894 17398 RMVar_ID_17398 Human_SNP_ID_594249337 A-to-I Human chr16 + 10404445 10404437 10404445 CTGCTGATTTTTAGTAGATACTGGGTTTCACCATGTTGGCCCGGCCGGTCTTGAACTCCTGACTT CTGCTGATTTTTAGTAGATACTGGG________TGTTGGCCCGGCCGGTCTTGAACTCCTGACTT GTTTCACCA G ATF7IP2 Ensembl:ENSG00000166669 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1165847870 Functional Loss DEL dbSNP153 26..33 33 - - - Human_RBP_ID_12662475 17399 RMVar_ID_17399 Human_SNP_ID_594258346 A-to-I Human chr16 - 10433399 10433399 10433399 AGGCTAAGGAGGGAGGGTGGCTTAAGGCCAGGAGTTCAAGACCAGCCTGGGCAACATAGTGAAAA AGGCTAAGGAGGGAGGGTGGCTTAAGGCCAGGGGTTCAAGACCAGCCTGGGCAACATAGTGAAAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1428700441 Functional Loss SNV dbSNP153 33..33 33 - - - 17400 RMVar_ID_17400 Human_SNP_ID_594260255 A-to-I Human chr16 + 10439321 10439321 10439321 GCGCGATCTCGGCTCACTGCAAGCTCTGCCTCAGGGTTCACACCATTCACCTGCCTCAGCCTACT GCGCGATCTCGGCTCACTGCAAGCTCTGCCTCCGGGTTCACACCATTCACCTGCCTCAGCCTACT A C ATF7IP2 Ensembl:ENSG00000166669 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1428489519 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7790,RMVar_hsa_circ_369037,RMVar_hsa_circ_36252,RMVar_hsa_circ_21149,RMVar_hsa_circ_326211,RMVar_hsa_circ_176192,RMVar_hsa_circ_364068,RMVar_hsa_circ_176194,RMVar_hsa_circ_41077,RMVar_hsa_circ_336256,RMVar_hsa_circ_57923,RMVar_hsa_circ_73743,RMVar_hsa_circ_58699,RMVar_hsa_circ_54525,RMVar_hsa_circ_360252,RMVar_hsa_circ_56545 17401 RMVar_ID_17401 Human_SNP_ID_594268166 A-to-I Human chr16 + 10465561 10465561 10465561 GGAATTTGACACCAGCCTGGGCAACACGGTGAAACCCCATCTCTACTAAAAACACAGAAAATTAG GGAATTTGACACCAGCCTGGGCAACACGGTGAGACCCCATCTCTACTAAAAACACAGAAAATTAG A G ATF7IP2 Ensembl:ENSG00000166669 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1199623392 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_369037,RMVar_hsa_circ_21149,RMVar_hsa_circ_41077,RMVar_hsa_circ_73743,RMVar_hsa_circ_58699,RMVar_hsa_circ_56545,RMVar_hsa_circ_65989 17402 RMVar_ID_17402 Human_SNP_ID_594269347 A-to-I Human chr16 + 10469728 10469728 10469728 AACCAAGGAGGCAGAGGTTGCGGTGAGCCGAGATCATGCCACTGCACTCCAGCCTGGGAAACGAG AACCAAGGAGGCAGAGGTTGCGGTGAGCCGAGTTCATGCCACTGCACTCCAGCCTGGGAAACGAG A T ATF7IP2 Ensembl:ENSG00000166669 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1177570691 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_369037,RMVar_hsa_circ_21149,RMVar_hsa_circ_41077,RMVar_hsa_circ_73743,RMVar_hsa_circ_58699,RMVar_hsa_circ_56545,RMVar_hsa_circ_65989 17403 RMVar_ID_17403 Human_SNP_ID_594282850 A-to-I Human chr16 - 10510263 10510263 10510263 AATCTCCTGGACTTAGGTGATCCTCCCAACTCAGCCTCCTGAGTAGCTGGGACTACAGGTGTGGG AATCTCCTGGACTTAGGTGATCCTCCCAACTCGGCCTCCTGAGTAGCTGGGACTACAGGTGTGGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs912183489 Functional Loss SNV dbSNP153 33..33 33 - - - 17404 RMVar_ID_17404 Human_SNP_ID_594286920 A-to-I Human chr16 - 10522058 10522058 10522058 CTGAAATGATCTGCCCATCTCAGCCTCCCAAAATGTTGGGATTACAGGCATGAGCCACCACGCCC CTGAAATGATCTGCCCATCTCAGCCTCCCAAAGTGTTGGGATTACAGGCATGAGCCACCACGCCC T C LINC01290 Ensembl:ENSG00000260468 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1414965563 Functional Loss SNV dbSNP153 33..33 33 - - - 17405 RMVar_ID_17405 Human_SNP_ID_594289373 A-to-I Human chr16 - 10529726 10529726 10529726 GGGTTTCTCCATGTTGGTCAGGCTGGTTTCGAACTCCCAACCTCAGGTGATCCGCCCACCTCAGC GGGTTTCTCCATGTTGGTCAGGCTGGTTTCGATCTCCCAACCTCAGGTGATCCGCCCACCTCAGC T A EMP2 Ensembl:ENSG00000213853 Protein coding 3'UTR GSE47997;GSE100210;GSE99789 K562 cells&HepG2 cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 23474544,29129909,29796672 RNA-Seq:(High) rs557929123 Functional Loss SNV dbSNP153 33..33 33 - - - 17406 RMVar_ID_17406 Human_SNP_ID_594289374 A-to-I Human chr16 - 10529726 10529726 10529726 GGGTTTCTCCATGTTGGTCAGGCTGGTTTCGAACTCCCAACCTCAGGTGATCCGCCCACCTCAGC GGGTTTCTCCATGTTGGTCAGGCTGGTTTCGACCTCCCAACCTCAGGTGATCCGCCCACCTCAGC T G EMP2 Ensembl:ENSG00000213853 Protein coding 3'UTR GSE47997;GSE100210;GSE99789 K562 cells&HepG2 cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 23474544,29129909,29796672 RNA-Seq:(High) rs557929123 Functional Loss SNV dbSNP153 33..33 33 - - - 17407 RMVar_ID_17407 Human_SNP_ID_594289415 A-to-I Human chr16 - 10529848 10529848 10529848 TGGCTCACCGCAACCTCTGCCTCCTGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCT TGGCTCACCGCAACCTCTGCCTCCTGGGTTCAGGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCT T C EMP2 Ensembl:ENSG00000213853 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line - 31158229,32596459 RNA-Seq:(High) rs1312898312 Functional Loss SNV dbSNP153 33..33 33 - - - 17408 RMVar_ID_17408 Human_SNP_ID_594289876 A-to-I Human chr16 - 10531348 10531348 10531348 AGCCTGGGTGACAGAGTGAGACTCCATCTCAAAAAAAGAAAAAAAAGAAAAGAAACTAATTACAC AGCCTGGGTGACAGAGTGAGACTCCATCTCAAGAAAAGAAAAAAAAGAAAAGAAACTAATTACAC T C EMP2 Ensembl:ENSG00000213853 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs367727964 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_182335 17409 RMVar_ID_17409 Human_SNP_ID_594289911 A-to-I Human chr16 - 10531459 10531459 10531459 GGGCGTGGTGGTGCATGCCTGTAATCCCAGCTATCAGGTGGCTGAGGCAGGAGAATCACTTGAAA GGGCGTGGTGGTGCATGCCTGTAATCCCAGCTTTCAGGTGGCTGAGGCAGGAGAATCACTTGAAA T A EMP2 Ensembl:ENSG00000213853 Protein coding 3'UTR GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs552639369 Functional Loss SNV dbSNP153 33..33 33 - - - 17410 RMVar_ID_17410 Human_SNP_ID_594289912 A-to-I Human chr16 - 10531459 10531459 10531459 GGGCGTGGTGGTGCATGCCTGTAATCCCAGCTATCAGGTGGCTGAGGCAGGAGAATCACTTGAAA GGGCGTGGTGGTGCATGCCTGTAATCCCAGCTGTCAGGTGGCTGAGGCAGGAGAATCACTTGAAA T C EMP2 Ensembl:ENSG00000213853 Protein coding 3'UTR GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs552639369 Functional Loss SNV dbSNP153 33..33 33 - - - 17411 RMVar_ID_17411 Human_SNP_ID_594289913 A-to-I Human chr16 - 10531469 10531469 10531469 AAAATGAGCTGGGCGTGGTGGTGCATGCCTGTAATCCCAGCTATCAGGTGGCTGAGGCAGGAGAA AAAATGAGCTGGGCGTGGTGGTGCATGCCTGTGATCCCAGCTATCAGGTGGCTGAGGCAGGAGAA T C EMP2 Ensembl:ENSG00000213853 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1244550674 Functional Loss SNV dbSNP153 33..33 33 - - - 17412 RMVar_ID_17412 Human_SNP_ID_594289931 A-to-I Human chr16 - 10531508 10531508 10531508 CTGGCCAAAATGGTAAAACCTGTCTCTACTAAAAATACAAAAATGAGCTGGGCGTGGTGGTGCAT CTGGCCAAAATGGTAAAACCTGTCTCTACTAAGAATACAAAAATGAGCTGGGCGTGGTGGTGCAT T C EMP2 Ensembl:ENSG00000213853 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1250350957 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_182336 17413 RMVar_ID_17413 Human_SNP_ID_594289932 A-to-I Human chr16 - 10531510 10531510 10531510 GCCTGGCCAAAATGGTAAAACCTGTCTCTACTAAAAATACAAAAATGAGCTGGGCGTGGTGGTGC GCCTGGCCAAAATGGTAAAACCTGTCTCTACTGAAAATACAAAAATGAGCTGGGCGTGGTGGTGC T C EMP2 Ensembl:ENSG00000213853 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1179419564 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_182336 17414 RMVar_ID_17414 Human_SNP_ID_594289937 A-to-I Human chr16 - 10531525 10531525 10531525 AGGAGTTCAAGACCAGCCTGGCCAAAATGGTAAAACCTGTCTCTACTAAAAATACAAAAATGAGC AGGAGTTCAAGACCAGCCTGGCCAAAATGGTAGAACCTGTCTCTACTAAAAATACAAAAATGAGC T C EMP2 Ensembl:ENSG00000213853 Protein coding 3'UTR GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs1262872795 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_182336 17415 RMVar_ID_17415 Human_SNP_ID_594289940 A-to-I Human chr16 - 10531531 10531531 10531531 GAGGTCAGGAGTTCAAGACCAGCCTGGCCAAAATGGTAAAACCTGTCTCTACTAAAAATACAAAA GAGGTCAGGAGTTCAAGACCAGCCTGGCCAAACTGGTAAAACCTGTCTCTACTAAAAATACAAAA T G EMP2 Ensembl:ENSG00000213853 Protein coding 3'UTR GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs991817092 Functional Loss SNV dbSNP153 33..33 33 - - - 17416 RMVar_ID_17416 Human_SNP_ID_594289970 A-to-I Human chr16 - 10531603 10531603 10531603 AAAACTGGCTGGGTACAGTGGCTCATGCTTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGTGG AAAACTGGCTGGGTACAGTGGCTCATGCTTGTGATCCCAGCACTTTGGGAGGCTGAGGCGGGTGG T C EMP2 Ensembl:ENSG00000213853 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947327471 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_129349 17417 RMVar_ID_17417 Human_SNP_ID_594291283 A-to-I Human chr16 - 10535500 10535497 10535500 TGTGCAGGCTGGTCTCGCAATCTGCCAGCGTCAGCCTCTCAAAGTGTTGGGATTCCGAGCATGAG TGTGCAGGCTGGTCTCGCAATCTGCCAGCGTC___CTCTCAAAGTGTTGGGATTCCGAGCATGAG GGCT G EMP2 Ensembl:ENSG00000213853 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1165924078 Functional Loss DEL dbSNP153 33..35 33 - - - 17418 RMVar_ID_17418 Human_SNP_ID_594291288 A-to-I Human chr16 - 10535513 10535513 10535513 GGTTTCACTATGTTGTGCAGGCTGGTCTCGCAATCTGCCAGCGTCAGCCTCTCAAAGTGTTGGGA GGTTTCACTATGTTGTGCAGGCTGGTCTCGCAGTCTGCCAGCGTCAGCCTCTCAAAGTGTTGGGA T C EMP2 Ensembl:ENSG00000213853 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs551060496 Functional Loss SNV dbSNP153 33..33 33 - - - 17419 RMVar_ID_17419 Human_SNP_ID_594294141 A-to-I Human chr16 - 10544363 10544363 10544363 TAGTCTGACCAACATGGCGAAACCCTGTCTCTACTAAAAATACAAAAATGAGCCAGGTGTGCTGG TAGTCTGACCAACATGGCGAAACCCTGTCTCTGCTAAAAATACAAAAATGAGCCAGGTGTGCTGG T C EMP2 Ensembl:ENSG00000213853 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1478126061 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_354564,RMVar_hsa_circ_301051 17420 RMVar_ID_17420 Human_SNP_ID_594312452 A-to-I Human chr16 - 10605789 10605789 10605789 GCAGCTACTTGAGAGGCTGAGGTGGGAGTATCACTTGAGCCCGGGGGTTTGAGGCTGCAGTGAGC GCAGCTACTTGAGAGGCTGAGGTGGGAGTATCCCTTGAGCCCGGGGGTTTGAGGCTGCAGTGAGC T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1450453271 Functional Loss SNV dbSNP153 33..33 33 - - - 17421 RMVar_ID_17421 Human_SNP_ID_594411214 A-to-I Human chr16 + 10913521 10913521 10913521 TATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGGTCTCAATCTTCTGACCTCGTGA TATTTTTAGTAGAGACGGGGTTTCACCGTGTTGGCCAGGATGGTCTCAATCTTCTGACCTCGTGA A G CIITA Ensembl:ENSG00000179583 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1452643139 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266563,RMVar_hsa_circ_77472,RMVar_hsa_circ_75236,RMVar_hsa_circ_108523,RMVar_hsa_circ_176217,RMVar_hsa_circ_361786,RMVar_hsa_circ_176218,RMVar_hsa_circ_111501,RMVar_hsa_circ_176219 17422 RMVar_ID_17422 Human_SNP_ID_594413124 A-to-I Human chr16 + 10919697 10919697 10919697 TGTTAATTTCTTCCCAGCATGATCACTGTTTTACAATATTTTATTTATGTAGGTGCTTACTTCTT TGTTAATTTCTTCCCAGCATGATCACTGTTTTGCAATATTTTATTTATGTAGGTGCTTACTTCTT A G CIITA Ensembl:ENSG00000179583 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs190816691 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266563 17423 RMVar_ID_17423 Human_SNP_ID_594414514 A-to-I Human chr16 + 10924373 10924373 10924373 CTTCTGCTTCAGCCTCCCGAGTAGCTGGGACTACAGGCACCCACCATCATGTCTGGCTAATTTTT CTTCTGCTTCAGCCTCCCGAGTAGCTGGGACTGCAGGCACCCACCATCATGTCTGGCTAATTTTT A G CIITA Ensembl:ENSG00000179583 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1313990599 Functional Loss SNV dbSNP153 33..33 33 - - - 17424 RMVar_ID_17424 Human_SNP_ID_594415083 A-to-I Human chr16 + 10926620 10926620 10926620 TGGAGTGCAGTGGCATGATCTCGGCTCACTGCAACCTCTGCCTCCTGGGTTCAAGCAATTCTCCC TGGAGTGCAGTGGCATGATCTCGGCTCACTGCCACCTCTGCCTCCTGGGTTCAAGCAATTCTCCC A C CIITA Ensembl:ENSG00000179583 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1262276207 Functional Loss SNV dbSNP153 33..33 33 - - - 17425 RMVar_ID_17425 Human_SNP_ID_594415552 A-to-I Human chr16 + 10928471 10928471 10928471 CCACTATGCCTGGCTAATTTTTTTGTATTTTTAGTAGAGATGGGGTTTCACCGTGGTGGCCAGGC CCACTATGCCTGGCTAATTTTTTTGTATTTTTCGTAGAGATGGGGTTTCACCGTGGTGGCCAGGC A C CIITA Ensembl:ENSG00000179583 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1453266284 Functional Loss SNV dbSNP153 33..33 33 - - - 17426 RMVar_ID_17426 Human_SNP_ID_594416274 A-to-I Human chr16 + 10931105 10931105 10931105 CCAGCACTTTGGGAGGCTGGGGTGGGAGGATCACTTGAGGCCAGGAGTTTGAGACCAGCCTGGGC CCAGCACTTTGGGAGGCTGGGGTGGGAGGATCCCTTGAGGCCAGGAGTTTGAGACCAGCCTGGGC A C CIITA Ensembl:ENSG00000179583 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1368556917 Functional Loss SNV dbSNP153 33..33 33 - - - 17427 RMVar_ID_17427 Human_SNP_ID_594416302 A-to-I Human chr16 - 10931203 10931198 10931203 GGCTCACGCAATCCTCCTGCCTCAGCCTTCCAAGTAGCTGAGACTACACTATGCCTGGCTAATTT GGCTCACGCAATCCTCCTGCCTCAGCCTTCCA_____CTGAGACTACACTATGCCTGGCTAATTT GCTACT G DEXI Ensembl:ENSG00000182108 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1437194840 Functional Loss DEL dbSNP153 33..37 33 - - - RMVar_hsa_circ_124032,RMVar_hsa_circ_176222 17428 RMVar_ID_17428 Human_SNP_ID_594416304 A-to-I Human chr16 - 10931203 10931203 10931203 GGCTCACGCAATCCTCCTGCCTCAGCCTTCCAAGTAGCTGAGACTACACTATGCCTGGCTAATTT GGCTCACGCAATCCTCCTGCCTCAGCCTTCCAGGTAGCTGAGACTACACTATGCCTGGCTAATTT T C DEXI Ensembl:ENSG00000182108 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs113207029 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124032,RMVar_hsa_circ_176222 17429 RMVar_ID_17429 Human_SNP_ID_594416414 A-to-I Human chr16 + 10931610 10931610 10931610 TCACACCTGTAATCCCAACACTTTGGGAGGCTAAGGTGGGTGGATCAGTTGAGATCAGGAGTTTG TCACACCTGTAATCCCAACACTTTGGGAGGCTGAGGTGGGTGGATCAGTTGAGATCAGGAGTTTG A G CIITA Ensembl:ENSG00000179583 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs966012765 Functional Loss SNV dbSNP153 33..33 33 - - - 17430 RMVar_ID_17430 Human_SNP_ID_594416476 A-to-I Human chr16 + 10931823 10931823 10931823 TGAGGCAGAAGAATCGCTTGAGCTAGGGAGGCAGAGGTTGCAGTGAGCCGAGATCACGCCACTGC TGAGGCAGAAGAATCGCTTGAGCTAGGGAGGCCGAGGTTGCAGTGAGCCGAGATCACGCCACTGC A C CIITA Ensembl:ENSG00000179583 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs367558904 Functional Loss SNV dbSNP153 33..33 33 - - - 17431 RMVar_ID_17431 Human_SNP_ID_594416746 A-to-I Human chr16 + 10932872 10932872 10932872 ACCATGCCTGGCTAATTGATGTATTTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTAA ACCATGCCTGGCTAATTGATGTATTTTTTAGTGGAGATGGGGTTTCACCATGTTGGCCAGGCTAA A G CIITA Ensembl:ENSG00000179583 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs895093157 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22003503 17432 RMVar_ID_17432 Human_SNP_ID_594416749 A-to-I Human chr16 + 10932886 10932886 10932886 ATTGATGTATTTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTAAAATCTCATAACGTT ATTGATGTATTTTTTAGTAGAGATGGGGTTTCGCCATGTTGGCCAGGCTAAAATCTCATAACGTT A G CIITA Ensembl:ENSG00000179583 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1409635515 Functional Loss SNV dbSNP153 33..33 33 - - - 17433 RMVar_ID_17433 Human_SNP_ID_594441637 A-to-I Human chr16 + 11016588 11016588 11016588 AAACTCTTGACCTCAAGGGATCCTCTTGCCTCAGCCTCCCAAAATGCTAGGATTACAGGCATGAG AAACTCTTGACCTCAAGGGATCCTCTTGCCTCGGCCTCCCAAAATGCTAGGATTACAGGCATGAG A G CLEC16A Ensembl:ENSG00000038532 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs766215584 Functional Loss SNV dbSNP153 33..33 33 - - - 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 17434 RMVar_ID_17434 Human_SNP_ID_594493632 A-to-I Human chr16 + 11181908 11181908 11181908 GATTTTGATCTTCTTGTCTAGATGCAATAAATAAATCTGAAGCATTTAATGTAGTCATCTTGACA GATTTTGATCTTCTTGTCTAGATGCAATAAATGAATCTGAAGCATTTAATGTAGTCATCTTGACA A G CLEC16A Ensembl:ENSG00000038532 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1055481717 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1837897,Human_RBP_ID_2467665,Human_RBP_ID_3491075 RMVar_hsa_circ_110672,RMVar_hsa_circ_176265 17435 RMVar_ID_17435 Human_SNP_ID_594537005 A-to-I Human chr16 + 11313965 11313965 11313965 GTTGGCCAGGCTGGTCTCAAACTTCTGGGCTCAAGCAATCTTCCTGCCTGGGCCCCTCAAAGTGT GTTGGCCAGGCTGGTCTCAAACTTCTGGGCTCTAGCAATCTTCCTGCCTGGGCCCCTCAAAGTGT A T RMI2 Ensembl:ENSG00000175643 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1216820036 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93358,RMVar_hsa_circ_176267 17436 RMVar_ID_17436 Human_SNP_ID_594538566 A-to-I Human chr16 + 11318479 11318479 11318479 GCTGGAGCCCAGCGGCATGATCATAGCTCACTACAGCCTCAACCTCCCTGACTCAAGCAATTCTC GCTGGAGCCCAGCGGCATGATCATAGCTCACTGCAGCCTCAACCTCCCTGACTCAAGCAATTCTC A G RMI2 Ensembl:ENSG00000175643 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs557186816 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93358,RMVar_hsa_circ_176267 17437 RMVar_ID_17437 Human_SNP_ID_594538582 A-to-I Human chr16 + 11318543 11318543 11318543 CCCTCCTCAGCCTCCTGAGTAGCTGAGACTACAGGCACGCACCACCACACCTGGCTAATTTTTTA CCCTCCTCAGCCTCCTGAGTAGCTGAGACTACCGGCACGCACCACCACACCTGGCTAATTTTTTA A C RMI2 Ensembl:ENSG00000175643 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1257697070 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93358,RMVar_hsa_circ_176267 17438 RMVar_ID_17438 Human_SNP_ID_594538603 A-to-I Human chr16 + 11318600 11318600 11318600 ATTTTTTATTTTTTGTAGAGTCAAGGCTCACTATGTTTCTGAGACTGGTCTGTAACTCCTGGACT ATTTTTTATTTTTTGTAGAGTCAAGGCTCACTGTGTTTCTGAGACTGGTCTGTAACTCCTGGACT A G RMI2 Ensembl:ENSG00000175643 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs761331305 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93358,RMVar_hsa_circ_176267 17439 RMVar_ID_17439 Human_SNP_ID_594585256 A-to-I Human chr16 - 11445969 11445969 11445969 AATATAAAAACTAGATGGGCATGGTGGTAGGTACCTGCAGTCCCAGCTACTCAGGAGGCTGAGGC AATATAAAAACTAGATGGGCATGGTGGTAGGTGCCTGCAGTCCCAGCTACTCAGGAGGCTGAGGC T C AC099489.1 Ensembl:ENSG00000188897 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs763640266 Functional Loss SNV dbSNP153 33..33 33 - - - 17440 RMVar_ID_17440 Human_SNP_ID_594623455 A-to-I Human chr16 - 11550277 11550277 11550277 GAGACCAGCCTGGCCAACACGGTGAAACCCCAACTCTCCTAATAATAAAAAAATTAGCTGGGCCT GAGACCAGCCTGGCCAACACGGTGAAACCCCAGCTCTCCTAATAATAAAAAAATTAGCTGGGCCT T C LITAF Ensembl:ENSG00000189067 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985938065 Functional Loss SNV dbSNP153 33..33 33 - - - 17441 RMVar_ID_17441 Human_SNP_ID_594625042 A-to-I Human chr16 - 11555246 11555246 11555246 GGCAGGAGGATCACCTGAGGCCAGGAGTTCCAAACCAGCCTGAGTGACATAGTGAGACATTGTCT GGCAGGAGGATCACCTGAGGCCAGGAGTTCCAGACCAGCCTGAGTGACATAGTGAGACATTGTCT T C LITAF Ensembl:ENSG00000189067 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1419223006 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24454,RMVar_hsa_circ_176273,RMVar_hsa_circ_274549 17442 RMVar_ID_17442 Human_SNP_ID_594626178 A-to-I Human chr16 - 11559065 11559065 11559065 TTTTTAAAATTTTGTAGAGAGAGGGTATCACTATGTTGTCTAGGCTGGTCTTGAACTCCTGGGCT TTTTTAAAATTTTGTAGAGAGAGGGTATCACTGTGTTGTCTAGGCTGGTCTTGAACTCCTGGGCT T C LITAF Ensembl:ENSG00000189067 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs892471518 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103083,RMVar_hsa_circ_176275 17443 RMVar_ID_17443 Human_SNP_ID_594627320 A-to-I Human chr16 - 11563107 11563107 11563107 TTTTTTGTGTAGAGATATGGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGTGTGATCACAGC TTTTTTGTGTAGAGATATGGTCTCACTCTGTCGCCCAGGCTGGAGTGCAGTGGTGTGATCACAGC T C LITAF Ensembl:ENSG00000189067 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388595866 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103083,RMVar_hsa_circ_176275 17444 RMVar_ID_17444 Human_SNP_ID_594629658 A-to-I Human chr16 - 11570842 11570842 11570842 GCAGCTGTGGCTCACTGCAGCCTCAACCCCCTAGACCCCACCCCCCAACCTCCTTCTACCTCAGC GCAGCTGTGGCTCACTGCAGCCTCAACCCCCTGGACCCCACCCCCCAACCTCCTTCTACCTCAGC T C LITAF Ensembl:ENSG00000189067 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs761395169 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103083,RMVar_hsa_circ_176275 17445 RMVar_ID_17445 Human_SNP_ID_594664069 A-to-I Human chr16 - 11681089 11681089 11681089 CGGCTCACTGCAGTCTTGAACTCCTGGACTCAAGTGATCCTCCCACCTCAGGCTCCTAAGTAGCT CGGCTCACTGCAGTCTTGAACTCCTGGACTCACGTGATCCTCCCACCTCAGGCTCCTAAGTAGCT T G TXNDC11 Ensembl:ENSG00000153066 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1173119424 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114608,RMVar_hsa_circ_176277 17446 RMVar_ID_17446 Human_SNP_ID_594665308 A-to-I Human chr16 - 11685244 11685244 11685244 CAGGTTCAGGTGATTCTCCCACCTTCCCAAGTAGCTGGGACTACAGGCATGTGCCAGAATACCCG CAGGTTCAGGTGATTCTCCCACCTTCCCAAGTGGCTGGGACTACAGGCATGTGCCAGAATACCCG T C TXNDC11 Ensembl:ENSG00000153066 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1024654909 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56868,RMVar_hsa_circ_322140,RMVar_hsa_circ_114608,RMVar_hsa_circ_330743,RMVar_hsa_circ_379089,RMVar_hsa_circ_176277,RMVar_hsa_circ_346031,RMVar_hsa_circ_325386,RMVar_hsa_circ_283616,RMVar_hsa_circ_307441,RMVar_hsa_circ_73670,RMVar_hsa_circ_176279,RMVar_hsa_circ_176281,RMVar_hsa_circ_176282,RMVar_hsa_circ_176283,RMVar_hsa_circ_176280,RMVar_hsa_circ_176278 17447 RMVar_ID_17447 Human_SNP_ID_594670273 A-to-I Human chr16 - 11701265 11701265 11701265 GGGTGTGGTGGCACACGCCTGTAATTGCAGCTACTTGGGAGGCTGAAGCAGGAGAATTGCTTGAG GGGTGTGGTGGCACACGCCTGTAATTGCAGCTGCTTGGGAGGCTGAAGCAGGAGAATTGCTTGAG T C TXNDC11 Ensembl:ENSG00000153066 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1376748299 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56868,RMVar_hsa_circ_114608,RMVar_hsa_circ_330743,RMVar_hsa_circ_176277,RMVar_hsa_circ_325386,RMVar_hsa_circ_73670,RMVar_hsa_circ_44967,RMVar_hsa_circ_176282,RMVar_hsa_circ_176283,RMVar_hsa_circ_370554,RMVar_hsa_circ_176284,RMVar_hsa_circ_68900,RMVar_hsa_circ_176288,RMVar_hsa_circ_273417,RMVar_hsa_circ_352680,RMVar_hsa_circ_305125,RMVar_hsa_circ_176289,RMVar_hsa_circ_377111 17448 RMVar_ID_17448 Human_SNP_ID_594672322 A-to-I Human chr16 - 11707830 11707830 11707830 GATCCTCCTGCCTCAGCCTCTCAAAACTGTTGAGATTATAGATGTGAGCTACCATACCCAGCCTA GATCCTCCTGCCTCAGCCTCTCAAAACTGTTGCGATTATAGATGTGAGCTACCATACCCAGCCTA T G TXNDC11 Ensembl:ENSG00000153066 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1567321307 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56868,RMVar_hsa_circ_114608,RMVar_hsa_circ_330743,RMVar_hsa_circ_176277,RMVar_hsa_circ_325386,RMVar_hsa_circ_44967,RMVar_hsa_circ_176282,RMVar_hsa_circ_176283,RMVar_hsa_circ_370554,RMVar_hsa_circ_176284,RMVar_hsa_circ_68900,RMVar_hsa_circ_176288,RMVar_hsa_circ_273417,RMVar_hsa_circ_352680,RMVar_hsa_circ_305125,RMVar_hsa_circ_176289,RMVar_hsa_circ_377111 17449 RMVar_ID_17449 Human_SNP_ID_594672333 A-to-I Human chr16 - 11707861 11707861 11707861 CCAGGCTGGTCTTGACCTCCTGGCCTCAAGTGATCCTCCTGCCTCAGCCTCTCAAAACTGTTGAG CCAGGCTGGTCTTGACCTCCTGGCCTCAAGTGGTCCTCCTGCCTCAGCCTCTCAAAACTGTTGAG T C TXNDC11 Ensembl:ENSG00000153066 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs865795853 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56868,RMVar_hsa_circ_114608,RMVar_hsa_circ_330743,RMVar_hsa_circ_176277,RMVar_hsa_circ_325386,RMVar_hsa_circ_44967,RMVar_hsa_circ_176282,RMVar_hsa_circ_176283,RMVar_hsa_circ_370554,RMVar_hsa_circ_176284,RMVar_hsa_circ_68900,RMVar_hsa_circ_176288,RMVar_hsa_circ_273417,RMVar_hsa_circ_352680,RMVar_hsa_circ_305125,RMVar_hsa_circ_176289,RMVar_hsa_circ_377111 17450 RMVar_ID_17450 Human_SNP_ID_594672378 A-to-I Human chr16 - 11707962 11707962 11707962 CTCCTGCATCAGCCTCCCAAGTAGCTAGGACTATAGGCTTACATCATCACGCTCAGCGAATTTTT CTCCTGCATCAGCCTCCCAAGTAGCTAGGACTGTAGGCTTACATCATCACGCTCAGCGAATTTTT T C TXNDC11 Ensembl:ENSG00000153066 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs769477557 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56868,RMVar_hsa_circ_114608,RMVar_hsa_circ_330743,RMVar_hsa_circ_176277,RMVar_hsa_circ_325386,RMVar_hsa_circ_44967,RMVar_hsa_circ_176282,RMVar_hsa_circ_176283,RMVar_hsa_circ_370554,RMVar_hsa_circ_176284,RMVar_hsa_circ_68900,RMVar_hsa_circ_176288,RMVar_hsa_circ_273417,RMVar_hsa_circ_352680,RMVar_hsa_circ_305125,RMVar_hsa_circ_176289,RMVar_hsa_circ_377111 17451 RMVar_ID_17451 Human_SNP_ID_594672379 A-to-I Human chr16 - 11707962 11707962 11707962 CTCCTGCATCAGCCTCCCAAGTAGCTAGGACTATAGGCTTACATCATCACGCTCAGCGAATTTTT CTCCTGCATCAGCCTCCCAAGTAGCTAGGACTCTAGGCTTACATCATCACGCTCAGCGAATTTTT T G TXNDC11 Ensembl:ENSG00000153066 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs769477557 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56868,RMVar_hsa_circ_114608,RMVar_hsa_circ_330743,RMVar_hsa_circ_176277,RMVar_hsa_circ_325386,RMVar_hsa_circ_44967,RMVar_hsa_circ_176282,RMVar_hsa_circ_176283,RMVar_hsa_circ_370554,RMVar_hsa_circ_176284,RMVar_hsa_circ_68900,RMVar_hsa_circ_176288,RMVar_hsa_circ_273417,RMVar_hsa_circ_352680,RMVar_hsa_circ_305125,RMVar_hsa_circ_176289,RMVar_hsa_circ_377111 17452 RMVar_ID_17452 Human_SNP_ID_594673062 A-to-I Human chr16 - 11710154 11710149 11710154 CATACAAGGGAAGTTTTTCAATTGATCATTTTATTTTTTCTTTTGAGATGGAGTCTTGCTCTGTC CATACAAGGGAAGTTTTTCAATTGATCATTTT_____TTCTTTTGAGATGGAGTCTTGCTCTGTC AAAAAT A TXNDC11 Ensembl:ENSG00000153066 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1452451268 Functional Loss DEL dbSNP153 33..37 33 - - - Human_RBP_ID_12664186 RMVar_hsa_circ_56868,RMVar_hsa_circ_114608,RMVar_hsa_circ_330743,RMVar_hsa_circ_176277,RMVar_hsa_circ_325386,RMVar_hsa_circ_44967,RMVar_hsa_circ_176282,RMVar_hsa_circ_176283,RMVar_hsa_circ_370554,RMVar_hsa_circ_176284,RMVar_hsa_circ_68900,RMVar_hsa_circ_176288,RMVar_hsa_circ_273417,RMVar_hsa_circ_352680,RMVar_hsa_circ_305125,RMVar_hsa_circ_176289,RMVar_hsa_circ_377111 17453 RMVar_ID_17453 Human_SNP_ID_594674955 A-to-I Human chr16 - 11716526 11716526 11716526 TAGATGATTAATTGTGGGCTGGCAATCTTTGTATATGTTTCAAAAGCCTGGAGGAAATCAGCTCT TAGATGATTAATTGTGGGCTGGCAATCTTTGTGTATGTTTCAAAAGCCTGGAGGAAATCAGCTCT T C TXNDC11 Ensembl:ENSG00000153066 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1592572 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_1244,GWAS_ID_1245,GWAS_ID_1246,GWAS_ID_1247,GWAS_ID_1248,GWAS_ID_1249,GWAS_ID_1250,GWAS_ID_1251,GWAS_ID_1252,GWAS_ID_1253,GWAS_ID_1254,GWAS_ID_1255,GWAS_ID_1256,GWAS_ID_1257,GWAS_ID_1258,GWAS_ID_1259,GWAS_ID_1260,GWAS_ID_1261,GWAS_ID_1262,GWAS_ID_1263,GWAS_ID_1264,GWAS_ID_1265,GWAS_ID_1266,GWAS_ID_1267,GWAS_ID_1268,GWAS_ID_1269,GWAS_ID_1270,GWAS_ID_1271,GWAS_ID_1272,GWAS_ID_1273,GWAS_ID_1274,GWAS_ID_1275,GWAS_ID_1276,GWAS_ID_1277 RMVar_hsa_circ_56868,RMVar_hsa_circ_114608,RMVar_hsa_circ_330743,RMVar_hsa_circ_176277,RMVar_hsa_circ_325386,RMVar_hsa_circ_44967,RMVar_hsa_circ_176282,RMVar_hsa_circ_176283,RMVar_hsa_circ_370554,RMVar_hsa_circ_176284,RMVar_hsa_circ_68900,RMVar_hsa_circ_176288,RMVar_hsa_circ_273417,RMVar_hsa_circ_352680,RMVar_hsa_circ_305125,RMVar_hsa_circ_176289,RMVar_hsa_circ_377111 17454 RMVar_ID_17454 Human_SNP_ID_594676123 A-to-I Human chr16 - 11720592 11720592 11720592 GCCAACATGACGAAACCCCGTCTCTACTAAAAATACAAAAATTTAGCCAGACATGGTGGCACGTG GCCAACATGACGAAACCCCGTCTCTACTAAAACTACAAAAATTTAGCCAGACATGGTGGCACGTG T G TXNDC11 Ensembl:ENSG00000153066 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1003031137 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56868,RMVar_hsa_circ_114608,RMVar_hsa_circ_330743,RMVar_hsa_circ_176277,RMVar_hsa_circ_325386,RMVar_hsa_circ_44967,RMVar_hsa_circ_176282,RMVar_hsa_circ_176283,RMVar_hsa_circ_370554,RMVar_hsa_circ_176284,RMVar_hsa_circ_68900,RMVar_hsa_circ_176288,RMVar_hsa_circ_273417,RMVar_hsa_circ_352680,RMVar_hsa_circ_305125,RMVar_hsa_circ_176289,RMVar_hsa_circ_377111 17455 RMVar_ID_17455 Human_SNP_ID_594676132 A-to-I Human chr16 - 11720618 11720618 11720618 GAGGTCAGGAGTTCGAGAACAGTCTGGCCAACATGACGAAACCCCGTCTCTACTAAAAATACAAA GAGGTCAGGAGTTCGAGAACAGTCTGGCCAACGTGACGAAACCCCGTCTCTACTAAAAATACAAA T C TXNDC11 Ensembl:ENSG00000153066 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs937509880 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56868,RMVar_hsa_circ_114608,RMVar_hsa_circ_330743,RMVar_hsa_circ_176277,RMVar_hsa_circ_325386,RMVar_hsa_circ_44967,RMVar_hsa_circ_176282,RMVar_hsa_circ_176283,RMVar_hsa_circ_370554,RMVar_hsa_circ_176284,RMVar_hsa_circ_68900,RMVar_hsa_circ_176288,RMVar_hsa_circ_273417,RMVar_hsa_circ_352680,RMVar_hsa_circ_305125,RMVar_hsa_circ_176289,RMVar_hsa_circ_377111 17456 RMVar_ID_17456 Human_SNP_ID_594676263 A-to-I Human chr16 - 11721015 11721015 11721015 GCTTGAGGCTGGGCGCAGTGGCTCATGCCCGTAGTCCCAGCACTTTGGGAGGCTTAGGCGGGTGG GCTTGAGGCTGGGCGCAGTGGCTCATGCCCGTGGTCCCAGCACTTTGGGAGGCTTAGGCGGGTGG T C TXNDC11 Ensembl:ENSG00000153066 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs986218259 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56868,RMVar_hsa_circ_114608,RMVar_hsa_circ_330743,RMVar_hsa_circ_176277,RMVar_hsa_circ_325386,RMVar_hsa_circ_44967,RMVar_hsa_circ_176282,RMVar_hsa_circ_176283,RMVar_hsa_circ_370554,RMVar_hsa_circ_176284,RMVar_hsa_circ_68900,RMVar_hsa_circ_176288,RMVar_hsa_circ_273417,RMVar_hsa_circ_352680,RMVar_hsa_circ_305125,RMVar_hsa_circ_176289,RMVar_hsa_circ_377111 17457 RMVar_ID_17457 Human_SNP_ID_594676403 A-to-I Human chr16 - 11721413 11721413 11721413 TTTTTTTTAGATGGAGTCTCGCCCTGCCGCCCAGGCTGGAGTGCAGTGGCGTGATCTTGGCTCAC TTTTTTTTAGATGGAGTCTCGCCCTGCCGCCCGGGCTGGAGTGCAGTGGCGTGATCTTGGCTCAC T C TXNDC11 Ensembl:ENSG00000153066 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs781310644 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17563958,Human_RBP_ID_23678137 Human_Splice_Rec_1678260,Human_Splice_Rec_1678261 RMVar_hsa_circ_56868,RMVar_hsa_circ_114608,RMVar_hsa_circ_330743,RMVar_hsa_circ_176277,RMVar_hsa_circ_325386,RMVar_hsa_circ_44967,RMVar_hsa_circ_176282,RMVar_hsa_circ_176283,RMVar_hsa_circ_370554,RMVar_hsa_circ_176284,RMVar_hsa_circ_68900,RMVar_hsa_circ_176288,RMVar_hsa_circ_273417,RMVar_hsa_circ_352680,RMVar_hsa_circ_305125,RMVar_hsa_circ_176289,RMVar_hsa_circ_377111 17458 RMVar_ID_17458 Human_SNP_ID_594677143 A-to-I Human chr16 - 11724117 11724117 11724117 CATCACGCCTGGCTAATTTTTGTGTTTTTAGTAGAGATGGGATTTCACCAGGCTGGCCAAGGGTG CATCACGCCTGGCTAATTTTTGTGTTTTTAGTGGAGATGGGATTTCACCAGGCTGGCCAAGGGTG T C TXNDC11 Ensembl:ENSG00000153066 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs899267415 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56868,RMVar_hsa_circ_325386,RMVar_hsa_circ_176283,RMVar_hsa_circ_370554,RMVar_hsa_circ_176284,RMVar_hsa_circ_68900,RMVar_hsa_circ_176291,RMVar_hsa_circ_273417,RMVar_hsa_circ_352680,RMVar_hsa_circ_176289,RMVar_hsa_circ_280684,RMVar_hsa_circ_305824,RMVar_hsa_circ_377111,RMVar_hsa_circ_288436,RMVar_hsa_circ_176292,RMVar_hsa_circ_176290 17459 RMVar_ID_17459 Human_SNP_ID_594677599 A-to-I Human chr16 - 11725911 11725911 11725911 TGATGGCACCACTGCACTCCATCCTGGGCAACAGAGTGAGACTCCATCTCAAAACAAAACAAAGA TGATGGCACCACTGCACTCCATCCTGGGCAACGGAGTGAGACTCCATCTCAAAACAAAACAAAGA T C TXNDC11 Ensembl:ENSG00000153066 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1291881847 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12664348 RMVar_hsa_circ_56868,RMVar_hsa_circ_325386,RMVar_hsa_circ_176283,RMVar_hsa_circ_370554,RMVar_hsa_circ_176284,RMVar_hsa_circ_68900,RMVar_hsa_circ_176291,RMVar_hsa_circ_273417,RMVar_hsa_circ_352680,RMVar_hsa_circ_176289,RMVar_hsa_circ_280684,RMVar_hsa_circ_305824,RMVar_hsa_circ_377111,RMVar_hsa_circ_288436,RMVar_hsa_circ_176292,RMVar_hsa_circ_176290 17460 RMVar_ID_17460 Human_SNP_ID_594685656 A-to-I Human chr16 - 11753502 11753502 11753502 AGGAGTTCAAGGCTGCAGTGAGCTATGATCGCACCACCATACTCTAGCCTGGATGACAGCGAGAC AGGAGTTCAAGGCTGCAGTGAGCTATGATCGCTCCACCATACTCTAGCCTGGATGACAGCGAGAC T A ZC3H7A Ensembl:ENSG00000122299 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903814532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12664571 RMVar_hsa_circ_119071,RMVar_hsa_circ_354903,RMVar_hsa_circ_341622,RMVar_hsa_circ_176299,RMVar_hsa_circ_28037,RMVar_hsa_circ_176298 17461 RMVar_ID_17461 Human_SNP_ID_594685829 A-to-I Human chr16 - 11754180 11754180 11754180 TCAGGTGATCCTCCGACCTCAGCCTCCTCAGTAGCTAGGACTGCAGGTGCTCTCCACCATGCCTG TCAGGTGATCCTCCGACCTCAGCCTCCTCAGTGGCTAGGACTGCAGGTGCTCTCCACCATGCCTG T C ZC3H7A Ensembl:ENSG00000122299 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1217795279 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12664581,Human_RBP_ID_25190499 RMVar_hsa_circ_119071,RMVar_hsa_circ_354903,RMVar_hsa_circ_341622,RMVar_hsa_circ_176299,RMVar_hsa_circ_28037,RMVar_hsa_circ_176298 17462 RMVar_ID_17462 Human_SNP_ID_594688855 A-to-I Human chr16 - 11764069 11764069 11764069 AAATGTAGGGCTGGGCTCCATGGCTCACGCCTATAATCCTAGCACTTTGGGAGGCCGAGGCAGGC AAATGTAGGGCTGGGCTCCATGGCTCACGCCTGTAATCCTAGCACTTTGGGAGGCCGAGGCAGGC T C ZC3H7A Ensembl:ENSG00000122299 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1316574884 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6825,RMVar_hsa_circ_119071,RMVar_hsa_circ_176299,RMVar_hsa_circ_69541,RMVar_hsa_circ_306144,RMVar_hsa_circ_118163,RMVar_hsa_circ_176302,RMVar_hsa_circ_48324,RMVar_hsa_circ_267879,RMVar_hsa_circ_176303,RMVar_hsa_circ_331854,RMVar_hsa_circ_321858,RMVar_hsa_circ_339619,RMVar_hsa_circ_352424,RMVar_hsa_circ_318473,RMVar_hsa_circ_314121,RMVar_hsa_circ_176307,RMVar_hsa_circ_33629,RMVar_hsa_circ_288923,RMVar_hsa_circ_176308,RMVar_hsa_circ_176305,RMVar_hsa_circ_176306,RMVar_hsa_circ_176304 17463 RMVar_ID_17463 Human_SNP_ID_594689021 A-to-I Human chr16 - 11764646 11764646 11764646 ATGATCTTGGCTCACTGCAAGTTCTGCCTCCCAGATTCAAGTGAATCTCCTGCCTCAGCCTCTCG ATGATCTTGGCTCACTGCAAGTTCTGCCTCCCCGATTCAAGTGAATCTCCTGCCTCAGCCTCTCG T G ZC3H7A Ensembl:ENSG00000122299 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs916401973 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6825,RMVar_hsa_circ_119071,RMVar_hsa_circ_176299,RMVar_hsa_circ_69541,RMVar_hsa_circ_306144,RMVar_hsa_circ_118163,RMVar_hsa_circ_176302,RMVar_hsa_circ_48324,RMVar_hsa_circ_267879,RMVar_hsa_circ_176303,RMVar_hsa_circ_331854,RMVar_hsa_circ_321858,RMVar_hsa_circ_339619,RMVar_hsa_circ_352424,RMVar_hsa_circ_318473,RMVar_hsa_circ_314121,RMVar_hsa_circ_176307,RMVar_hsa_circ_33629,RMVar_hsa_circ_288923,RMVar_hsa_circ_176308,RMVar_hsa_circ_176305,RMVar_hsa_circ_176306,RMVar_hsa_circ_176304 17464 RMVar_ID_17464 Human_SNP_ID_594690447 A-to-I Human chr16 - 11769628 11769628 11769628 TGGCTCACTGCAACCTCTGCCTCTTGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCT TGGCTCACTGCAACCTCTGCCTCTTGGGTTCAGGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCT T C ZC3H7A Ensembl:ENSG00000122299 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1015230617 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6825,RMVar_hsa_circ_69541,RMVar_hsa_circ_16401,RMVar_hsa_circ_306144,RMVar_hsa_circ_118163,RMVar_hsa_circ_176302,RMVar_hsa_circ_48324,RMVar_hsa_circ_267879,RMVar_hsa_circ_331854,RMVar_hsa_circ_321858,RMVar_hsa_circ_318473,RMVar_hsa_circ_33629,RMVar_hsa_circ_176305,RMVar_hsa_circ_176304,RMVar_hsa_circ_365175,RMVar_hsa_circ_176309,RMVar_hsa_circ_176310,RMVar_hsa_circ_326363,RMVar_hsa_circ_332717,RMVar_hsa_circ_176311,RMVar_hsa_circ_266067 17465 RMVar_ID_17465 Human_SNP_ID_594690453 A-to-I Human chr16 - 11769648 11769648 11769648 GGAAAGCAGTGGCGAAATCTTGGCTCACTGCAACCTCTGCCTCTTGGGTTCAAGCGATTCTCCTG GGAAAGCAGTGGCGAAATCTTGGCTCACTGCAGCCTCTGCCTCTTGGGTTCAAGCGATTCTCCTG T C ZC3H7A Ensembl:ENSG00000122299 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1476335954 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6825,RMVar_hsa_circ_69541,RMVar_hsa_circ_16401,RMVar_hsa_circ_306144,RMVar_hsa_circ_118163,RMVar_hsa_circ_176302,RMVar_hsa_circ_48324,RMVar_hsa_circ_267879,RMVar_hsa_circ_331854,RMVar_hsa_circ_321858,RMVar_hsa_circ_318473,RMVar_hsa_circ_33629,RMVar_hsa_circ_176305,RMVar_hsa_circ_176304,RMVar_hsa_circ_365175,RMVar_hsa_circ_176309,RMVar_hsa_circ_176310,RMVar_hsa_circ_326363,RMVar_hsa_circ_332717,RMVar_hsa_circ_176311,RMVar_hsa_circ_266067 17466 RMVar_ID_17466 Human_SNP_ID_594690616 A-to-I Human chr16 - 11769882 11769882 11769882 GGGAGGTGGAGGTGGGAGGATTCCTTGAGCCCAGGAGGTTGAGGCTGCAGTGAGCCAAGATCACA GGGAGGTGGAGGTGGGAGGATTCCTTGAGCCCGGGAGGTTGAGGCTGCAGTGAGCCAAGATCACA T C ZC3H7A Ensembl:ENSG00000122299 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs566024270 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6825,RMVar_hsa_circ_69541,RMVar_hsa_circ_16401,RMVar_hsa_circ_306144,RMVar_hsa_circ_118163,RMVar_hsa_circ_176302,RMVar_hsa_circ_48324,RMVar_hsa_circ_267879,RMVar_hsa_circ_331854,RMVar_hsa_circ_321858,RMVar_hsa_circ_318473,RMVar_hsa_circ_33629,RMVar_hsa_circ_176305,RMVar_hsa_circ_176304,RMVar_hsa_circ_365175,RMVar_hsa_circ_176309,RMVar_hsa_circ_176310,RMVar_hsa_circ_326363,RMVar_hsa_circ_332717,RMVar_hsa_circ_176311,RMVar_hsa_circ_266067 17467 RMVar_ID_17467 Human_SNP_ID_594691155 A-to-I Human chr16 - 11771697 11771697 11771697 CAGGAGTTTGAGACCAGCCTGGCCAACATGGCAAAACCCCATCTCTACTAAAAATACAAAAATTA CAGGAGTTTGAGACCAGCCTGGCCAACATGGCGAAACCCCATCTCTACTAAAAATACAAAAATTA T C ZC3H7A Ensembl:ENSG00000122299 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs61474095 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6825,RMVar_hsa_circ_69541,RMVar_hsa_circ_16401,RMVar_hsa_circ_306144,RMVar_hsa_circ_118163,RMVar_hsa_circ_176302,RMVar_hsa_circ_48324,RMVar_hsa_circ_267879,RMVar_hsa_circ_331854,RMVar_hsa_circ_318473,RMVar_hsa_circ_33629,RMVar_hsa_circ_176304,RMVar_hsa_circ_365175,RMVar_hsa_circ_55662,RMVar_hsa_circ_176309,RMVar_hsa_circ_176310,RMVar_hsa_circ_326363,RMVar_hsa_circ_332717,RMVar_hsa_circ_176311,RMVar_hsa_circ_372205,RMVar_hsa_circ_266067,RMVar_hsa_circ_341703,RMVar_hsa_circ_176312,RMVar_hsa_circ_176313 17468 RMVar_ID_17468 Human_SNP_ID_594691221 A-to-I Human chr16 - 11771944 11771944 11771944 GTGATCCACCCACCTCATCCTCCCACAGTGCTAGGATTACAGGTGTGAGCCACCATGCCCAGCCT GTGATCCACCCACCTCATCCTCCCACAGTGCTGGGATTACAGGTGTGAGCCACCATGCCCAGCCT T C ZC3H7A Ensembl:ENSG00000122299 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1009675269 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6825,RMVar_hsa_circ_69541,RMVar_hsa_circ_16401,RMVar_hsa_circ_306144,RMVar_hsa_circ_118163,RMVar_hsa_circ_176302,RMVar_hsa_circ_48324,RMVar_hsa_circ_267879,RMVar_hsa_circ_331854,RMVar_hsa_circ_318473,RMVar_hsa_circ_33629,RMVar_hsa_circ_176304,RMVar_hsa_circ_365175,RMVar_hsa_circ_55662,RMVar_hsa_circ_176309,RMVar_hsa_circ_176310,RMVar_hsa_circ_326363,RMVar_hsa_circ_332717,RMVar_hsa_circ_176311,RMVar_hsa_circ_372205,RMVar_hsa_circ_266067,RMVar_hsa_circ_341703,RMVar_hsa_circ_176312,RMVar_hsa_circ_176313 17469 RMVar_ID_17469 Human_SNP_ID_594691496 A-to-I Human chr16 - 11772834 11772834 11772834 AAATTAGCTGGGCATGGTGGTGCATATCTGTAATCGCAGCTACTTGGGTGGCTGAGGCAAGAGAA AAATTAGCTGGGCATGGTGGTGCATATCTGTAGTCGCAGCTACTTGGGTGGCTGAGGCAAGAGAA T C ZC3H7A Ensembl:ENSG00000122299 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1390673829 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6825,RMVar_hsa_circ_69541,RMVar_hsa_circ_16401,RMVar_hsa_circ_306144,RMVar_hsa_circ_118163,RMVar_hsa_circ_176302,RMVar_hsa_circ_48324,RMVar_hsa_circ_267879,RMVar_hsa_circ_331854,RMVar_hsa_circ_318473,RMVar_hsa_circ_33629,RMVar_hsa_circ_176304,RMVar_hsa_circ_365175,RMVar_hsa_circ_55662,RMVar_hsa_circ_176309,RMVar_hsa_circ_176310,RMVar_hsa_circ_326363,RMVar_hsa_circ_332717,RMVar_hsa_circ_176311,RMVar_hsa_circ_372205,RMVar_hsa_circ_266067,RMVar_hsa_circ_341703,RMVar_hsa_circ_176312,RMVar_hsa_circ_176313 17470 RMVar_ID_17470 Human_SNP_ID_594691740 A-to-I Human chr16 - 11773718 11773718 11773718 CCACCACGCCTGGCTAATTTTTTTGTATTTTTAGTAAAGATGGGGTTTCACTGCCTTAGCCAGAA CCACCACGCCTGGCTAATTTTTTTGTATTTTTGGTAAAGATGGGGTTTCACTGCCTTAGCCAGAA T C ZC3H7A Ensembl:ENSG00000122299 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1428293820 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6825,RMVar_hsa_circ_69541,RMVar_hsa_circ_16401,RMVar_hsa_circ_306144,RMVar_hsa_circ_118163,RMVar_hsa_circ_176302,RMVar_hsa_circ_48324,RMVar_hsa_circ_267879,RMVar_hsa_circ_331854,RMVar_hsa_circ_318473,RMVar_hsa_circ_33629,RMVar_hsa_circ_176304,RMVar_hsa_circ_365175,RMVar_hsa_circ_55662,RMVar_hsa_circ_176309,RMVar_hsa_circ_176310,RMVar_hsa_circ_326363,RMVar_hsa_circ_332717,RMVar_hsa_circ_176311,RMVar_hsa_circ_372205,RMVar_hsa_circ_266067,RMVar_hsa_circ_341703,RMVar_hsa_circ_176312,RMVar_hsa_circ_176313 17471 RMVar_ID_17471 Human_SNP_ID_594691745 A-to-I Human chr16 - 11773734 11773734 11773734 GGACTACAGGCGCCCGCCACCACGCCTGGCTAATTTTTTTGTATTTTTAGTAAAGATGGGGTTTC GGACTACAGGCGCCCGCCACCACGCCTGGCTACTTTTTTTGTATTTTTAGTAAAGATGGGGTTTC T G ZC3H7A Ensembl:ENSG00000122299 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1259126276 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6825,RMVar_hsa_circ_69541,RMVar_hsa_circ_16401,RMVar_hsa_circ_306144,RMVar_hsa_circ_118163,RMVar_hsa_circ_176302,RMVar_hsa_circ_48324,RMVar_hsa_circ_267879,RMVar_hsa_circ_331854,RMVar_hsa_circ_318473,RMVar_hsa_circ_33629,RMVar_hsa_circ_176304,RMVar_hsa_circ_365175,RMVar_hsa_circ_55662,RMVar_hsa_circ_176309,RMVar_hsa_circ_176310,RMVar_hsa_circ_326363,RMVar_hsa_circ_332717,RMVar_hsa_circ_176311,RMVar_hsa_circ_372205,RMVar_hsa_circ_266067,RMVar_hsa_circ_341703,RMVar_hsa_circ_176312,RMVar_hsa_circ_176313 17472 RMVar_ID_17472 Human_SNP_ID_594691746 A-to-I Human chr16 - 11773735 11773735 11773735 GGGACTACAGGCGCCCGCCACCACGCCTGGCTAATTTTTTTGTATTTTTAGTAAAGATGGGGTTT GGGACTACAGGCGCCCGCCACCACGCCTGGCTGATTTTTTTGTATTTTTAGTAAAGATGGGGTTT T C ZC3H7A Ensembl:ENSG00000122299 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1303757134 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6825,RMVar_hsa_circ_69541,RMVar_hsa_circ_16401,RMVar_hsa_circ_306144,RMVar_hsa_circ_118163,RMVar_hsa_circ_176302,RMVar_hsa_circ_48324,RMVar_hsa_circ_267879,RMVar_hsa_circ_331854,RMVar_hsa_circ_318473,RMVar_hsa_circ_33629,RMVar_hsa_circ_176304,RMVar_hsa_circ_365175,RMVar_hsa_circ_55662,RMVar_hsa_circ_176309,RMVar_hsa_circ_176310,RMVar_hsa_circ_326363,RMVar_hsa_circ_332717,RMVar_hsa_circ_176311,RMVar_hsa_circ_372205,RMVar_hsa_circ_266067,RMVar_hsa_circ_341703,RMVar_hsa_circ_176312,RMVar_hsa_circ_176313 17473 RMVar_ID_17473 Human_SNP_ID_594695884 A-to-I Human chr16 - 11787186 11787186 11787186 TCAGTCCTCTTGCCTTAGCCTCCTGAGTAGCTAGGACTACAGGCACGTACCACCACACCTGGCTT TCAGTCCTCTTGCCTTAGCCTCCTGAGTAGCTTGGACTACAGGCACGTACCACCACACCTGGCTT T A ZC3H7A Ensembl:ENSG00000122299 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs891213534 Functional Loss SNV dbSNP153 33..33 33 - - - 17474 RMVar_ID_17474 Human_SNP_ID_594695885 A-to-I Human chr16 - 11787186 11787186 11787186 TCAGTCCTCTTGCCTTAGCCTCCTGAGTAGCTAGGACTACAGGCACGTACCACCACACCTGGCTT TCAGTCCTCTTGCCTTAGCCTCCTGAGTAGCTGGGACTACAGGCACGTACCACCACACCTGGCTT T C ZC3H7A Ensembl:ENSG00000122299 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs891213534 Functional Loss SNV dbSNP153 33..33 33 - - - 17475 RMVar_ID_17475 Human_SNP_ID_594695995 A-to-I Human chr16 - 11787586 11787586 11787586 GCATGGTGGCACACTTGTAGTCTCAGCTACTCAGGAGGCTGATGAGGGAGGATCGCTTGAGACCG GCATGGTGGCACACTTGTAGTCTCAGCTACTCCGGAGGCTGATGAGGGAGGATCGCTTGAGACCG T G ZC3H7A Ensembl:ENSG00000122299 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs772745202 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17563962 17476 RMVar_ID_17476 Human_SNP_ID_594696627 A-to-I Human chr16 - 11789419 11789419 11789419 TGAAACCCCATCTCTACAAAAATACAAAAATTAGCCAGGCCTGGTGACGTGCGCCTGTAATCCCA TGAAACCCCATCTCTACAAAAATACAAAAATTGGCCAGGCCTGGTGACGTGCGCCTGTAATCCCA T C ZC3H7A Ensembl:ENSG00000122299 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1257889130 Functional Loss SNV dbSNP153 33..33 33 - - - 17477 RMVar_ID_17477 Human_SNP_ID_594697516 A-to-I Human chr16 - 11792062 11792062 11792062 CTCTACAAAAAATACAAAAATTATTCAGGTATAGTGGCATGTGCTTGTAGTTCCAGCTACTTGGG CTCTACAAAAAATACAAAAATTATTCAGGTATTGTGGCATGTGCTTGTAGTTCCAGCTACTTGGG T A ZC3H7A Ensembl:ENSG00000122299 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs921083104 Functional Loss SNV dbSNP153 33..33 33 - - - 17478 RMVar_ID_17478 Human_SNP_ID_594698650 A-to-I Human chr16 - 11796032 11796032 11796032 GTGCAGGAGTTCAAGACCAGCCTCAGCAACATAGTGAGACCCCTGTCTCTACAAAAAATACAAAA GTGCAGGAGTTCAAGACCAGCCTCAGCAACATCGTGAGACCCCTGTCTCTACAAAAAATACAAAA T G ZC3H7A Ensembl:ENSG00000122299 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs955194870 Functional Loss SNV dbSNP153 33..33 33 - - - 17479 RMVar_ID_17479 Human_SNP_ID_594700098 A-to-I Human chr16 + 11799930 11799930 11799930 AGTCTGTCACCCAGGCTGGAGTACAGAGGCGCAATCATGGCTCACTGCAGTCTTGATCTCCCGGG AGTCTGTCACCCAGGCTGGAGTACAGAGGCGCCATCATGGCTCACTGCAGTCTTGATCTCCCGGG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs936739787 Functional Loss SNV dbSNP153 33..33 33 - - - 17480 RMVar_ID_17480 Human_SNP_ID_594700135 A-to-I Human chr16 + 11800056 11800055 11800057 GTTTTTGGGGTTTTTTTTGTTTTTGTAGAGACAGGGTTTTGCCATGTTGCCCAGGCTGGTCCCAA GTTTTTGGGGTTTTTTTTGTTTTTGTAGAGAC__GGTTTTGCCATGTTGCCCAGGCTGGTCCCAA CAG C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1434414079 Functional Loss DEL dbSNP153 33..34 33 - - - 17481 RMVar_ID_17481 Human_SNP_ID_594700141 A-to-I Human chr16 + 11800076 11800075 11800076 TTTTGTAGAGACAGGGTTTTGCCATGTTGCCCAGGCTGGTCCCAAACTCCTGGGCTCAAGCAGTC TTTTGTAGAGACAGGGTTTTGCCATGTTGCCC_GGCTGGTCCCAAACTCCTGGGCTCAAGCAGTC CA C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1455108052 Functional Loss DEL dbSNP153 33..33 33 - - - 17482 RMVar_ID_17482 Human_SNP_ID_594700329 A-to-I Human chr16 - 11800786 11800786 11800786 CAACATGGAGAAACCCCGTCTCTACTAAAAATACAAAAATCAGCCGGGTGAGGTGGCGGCGCACG CAACATGGAGAAACCCCGTCTCTACTAAAAATGCAAAAATCAGCCGGGTGAGGTGGCGGCGCACG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1318002727 Functional Loss SNV dbSNP153 33..33 33 - - - 17483 RMVar_ID_17483 Human_SNP_ID_594712103 A-to-I Human chr16 - 11835293 11835293 11835293 CCTGTAATCCCAGCTACTTGGGAGGCTGAAGCAGGAGAATCACTTTAACCCGGGAGGTGGAGGTT CCTGTAATCCCAGCTACTTGGGAGGCTGAAGCCGGAGAATCACTTTAACCCGGGAGGTGGAGGTT T G RSL1D1 Ensembl:ENSG00000171490 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1194059431 Functional Loss SNV dbSNP153 33..33 33 - - - 17484 RMVar_ID_17484 Human_SNP_ID_594712111 A-to-I Human chr16 - 11835319 11835319 11835319 AAACTAGCCAGGCATGGTGGGAGGCACCTGTAATCCCAGCTACTTGGGAGGCTGAAGCAGGAGAA AAACTAGCCAGGCATGGTGGGAGGCACCTGTAGTCCCAGCTACTTGGGAGGCTGAAGCAGGAGAA T C RSL1D1 Ensembl:ENSG00000171490 Protein coding 3'UTR GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs946211202 Functional Loss SNV dbSNP153 33..33 33 - - - 17485 RMVar_ID_17485 Human_SNP_ID_594712756 A-to-I Human chr16 - 11837106 11837106 11837106 AGTGTGGCATGGTGGCATGCATCTGTGCTCCCAGCTCCTCACGAGGCTGAGGTGGAAGGATCAAG AGTGTGGCATGGTGGCATGCATCTGTGCTCCCGGCTCCTCACGAGGCTGAGGTGGAAGGATCAAG T C RSL1D1 Ensembl:ENSG00000171490 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1003332932 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6492980 17486 RMVar_ID_17486 Human_SNP_ID_594712897 A-to-I Human chr16 - 11837507 11837507 11837507 GTCTGTACCAAAAATACAAAAATTAATTGGGCATGGTGGTGGACACCTGTAATCCCAGCTACTAG GTCTGTACCAAAAATACAAAAATTAATTGGGCCTGGTGGTGGACACCTGTAATCCCAGCTACTAG T G RSL1D1 Ensembl:ENSG00000171490 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1311006903 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_468142,Human_RBP_ID_1837980,Human_RBP_ID_8187669,Human_RBP_ID_17252882 17487 RMVar_ID_17487 Human_SNP_ID_594712913 A-to-I Human chr16 - 11837552 11837552 11837552 AGGTCAACGAGATCGAGACCATCCTGGCCAACATGGTGAAACCCTGTCTGTACCAAAAATACAAA AGGTCAACGAGATCGAGACCATCCTGGCCAACTTGGTGAAACCCTGTCTGTACCAAAAATACAAA T A RSL1D1 Ensembl:ENSG00000171490 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1354845075 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1512221,Human_RBP_ID_1837981,Human_RBP_ID_4350220,Human_RBP_ID_12665369,Human_RBP_ID_26811018,Human_RBP_ID_27438995 17488 RMVar_ID_17488 Human_SNP_ID_594712914 A-to-I Human chr16 - 11837552 11837552 11837552 AGGTCAACGAGATCGAGACCATCCTGGCCAACATGGTGAAACCCTGTCTGTACCAAAAATACAAA AGGTCAACGAGATCGAGACCATCCTGGCCAACGTGGTGAAACCCTGTCTGTACCAAAAATACAAA T C RSL1D1 Ensembl:ENSG00000171490 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1354845075 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1512221,Human_RBP_ID_1837981,Human_RBP_ID_4350220,Human_RBP_ID_12665369,Human_RBP_ID_26811018,Human_RBP_ID_27438995 17489 RMVar_ID_17489 Human_SNP_ID_594712916 A-to-I Human chr16 - 11837554 11837554 11837554 CAAGGTCAACGAGATCGAGACCATCCTGGCCAACATGGTGAAACCCTGTCTGTACCAAAAATACA CAAGGTCAACGAGATCGAGACCATCCTGGCCAGCATGGTGAAACCCTGTCTGTACCAAAAATACA T C RSL1D1 Ensembl:ENSG00000171490 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs113393544 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1512221,Human_RBP_ID_1837981,Human_RBP_ID_12665369,Human_RBP_ID_26811018,Human_RBP_ID_27438995 17490 RMVar_ID_17490 Human_SNP_ID_594712917 A-to-I Human chr16 - 11837554 11837554 11837554 CAAGGTCAACGAGATCGAGACCATCCTGGCCAACATGGTGAAACCCTGTCTGTACCAAAAATACA CAAGGTCAACGAGATCGAGACCATCCTGGCCACCATGGTGAAACCCTGTCTGTACCAAAAATACA T G RSL1D1 Ensembl:ENSG00000171490 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs113393544 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1512221,Human_RBP_ID_1837981,Human_RBP_ID_12665369,Human_RBP_ID_26811018,Human_RBP_ID_27438995 17491 RMVar_ID_17491 Human_SNP_ID_594712943 A-to-I Human chr16 - 11837622 11837622 11837622 AAGTAGTCCAGGGGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGCGGA AAGTAGTCCAGGGGCGGTGGCTCACGCCTGTAGTCCCAGCACTTTGGGAGGCCGAGGCAGGCGGA T C RSL1D1 Ensembl:ENSG00000171490 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1370738062 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_235113,Human_RBP_ID_468145,Human_RBP_ID_762897,Human_RBP_ID_8185754,Human_RBP_ID_9372272,Human_RBP_ID_22705749,Human_RBP_ID_26328059 17492 RMVar_ID_17492 Human_SNP_ID_594713224 A-to-I Human chr16 - 11838302 11838302 11838302 AAAAAATGAGCCGGGCGTGGTGGCACACACCTATAATACCAGCTACTCGGGAGGCAGAGGTTGCA AAAAAATGAGCCGGGCGTGGTGGCACACACCTGTAATACCAGCTACTCGGGAGGCAGAGGTTGCA T C RSL1D1 Ensembl:ENSG00000171490 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs375725732 Functional Loss SNV dbSNP153 33..33 33 - - - 17493 RMVar_ID_17493 Human_SNP_ID_594713359 A-to-I Human chr16 - 11838694 11838694 11838694 TGCCAACATGCCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTTGCCATGTTGGCCAGGC TGCCAACATGCCTGGCTAATTTTTGTATTTTTGGTAGAGATGGGGTTTTGCCATGTTGGCCAGGC T C RSL1D1 Ensembl:ENSG00000171490 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1179703037 Functional Loss SNV dbSNP153 33..33 33 - - - 17494 RMVar_ID_17494 Human_SNP_ID_594713403 A-to-I Human chr16 - 11838819 11838819 11838819 AAGGTCTCACTTTGTTGCCCAGGATGGAGTGCAGTGGCATGATCTCGGCTCACAGCAACCTCCAC AAGGTCTCACTTTGTTGCCCAGGATGGAGTGCGGTGGCATGATCTCGGCTCACAGCAACCTCCAC T C RSL1D1 Ensembl:ENSG00000171490 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1219278560 Functional Loss SNV dbSNP153 33..33 33 - - - 17495 RMVar_ID_17495 Human_SNP_ID_594714897 A-to-I Human chr16 - 11842861 11842861 11842861 ATCTCAGCTACTAGGGAGGCTGAGGCAGGAGAATTGCTTGAACCCAGGAGGCGAAGGTTGCAGTG ATCTCAGCTACTAGGGAGGCTGAGGCAGGAGAGTTGCTTGAACCCAGGAGGCGAAGGTTGCAGTG T C RSL1D1 Ensembl:ENSG00000171490 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs375113550 Functional Loss SNV dbSNP153 33..33 33 - - - 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 17496 RMVar_ID_17496 Human_SNP_ID_594714911 A-to-I Human chr16 - 11842893 11842892 11842893 AAATTAGCTGGGCGTGGTGGCATGCGCCTGTAATCTCAGCTACTAGGGAGGCTGAGGCAGGAGAA AAATTAGCTGGGCGTGGTGGCATGCGCCTGTA_TCTCAGCTACTAGGGAGGCTGAGGCAGGAGAA AT A RSL1D1 Ensembl:ENSG00000171490 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1490051182 Functional Loss DEL dbSNP153 33..33 33 - - - 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 17497 RMVar_ID_17497 Human_SNP_ID_594715084 A-to-I Human chr16 - 11843270 11843270 11843270 GGGCAGGTGTTTGAGACCAGTCTGGCCAACACAGTGAAACCCCATCTCTACTAAAAATACACAAA GGGCAGGTGTTTGAGACCAGTCTGGCCAACACGGTGAAACCCCATCTCTACTAAAAATACACAAA T C RSL1D1 Ensembl:ENSG00000171490 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs372712901 Functional Loss SNV dbSNP153 33..33 33 - - - 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 17498 RMVar_ID_17498 Human_SNP_ID_594715287 A-to-I Human chr16 - 11843819 11843819 11843819 TCGCCCAGGCTAGAGTGCAGTGGCTTGATCTCAGCTCACTGCAAGCTCCGCCTGCCGGGTTCACA TCGCCCAGGCTAGAGTGCAGTGGCTTGATCTCTGCTCACTGCAAGCTCCGCCTGCCGGGTTCACA T A RSL1D1 Ensembl:ENSG00000171490 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs554625280 Functional Loss SNV dbSNP153 33..33 33 - - - 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 17499 RMVar_ID_17499 Human_SNP_ID_594715288 A-to-I Human chr16 - 11843819 11843819 11843819 TCGCCCAGGCTAGAGTGCAGTGGCTTGATCTCAGCTCACTGCAAGCTCCGCCTGCCGGGTTCACA TCGCCCAGGCTAGAGTGCAGTGGCTTGATCTCGGCTCACTGCAAGCTCCGCCTGCCGGGTTCACA T C RSL1D1 Ensembl:ENSG00000171490 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs554625280 Functional Loss SNV dbSNP153 33..33 33 - - - 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 17500 RMVar_ID_17500 Human_SNP_ID_594715297 A-to-I Human chr16 - 11843840 11843840 11843840 TGAGACAGAGTTCTTGCTCTGTCGCCCAGGCTAGAGTGCAGTGGCTTGATCTCAGCTCACTGCAA TGAGACAGAGTTCTTGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCTTGATCTCAGCTCACTGCAA T C RSL1D1 Ensembl:ENSG00000171490 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1567419547 Functional Loss SNV dbSNP153 33..33 33 - - - 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 17501 RMVar_ID_17501 Human_SNP_ID_594715954 A-to-I Human chr16 - 11845846 11845846 11845846 GTGGTGGTGCATCCCTGTGCTCCCAGCTACACAGGAGGCTGTGGCAGGAGGATCACTTGAGCCTA GTGGTGGTGCATCCCTGTGCTCCCAGCTACACGGGAGGCTGTGGCAGGAGGATCACTTGAGCCTA T C RSL1D1 Ensembl:ENSG00000171490 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs546661839 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17563966 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 17502 RMVar_ID_17502 Human_SNP_ID_594716837 A-to-I Human chr16 - 11848072 11848072 11848072 ATTTTTTATAATTTTAGTAGAAACAGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGA ATTTTTTATAATTTTAGTAGAAACAGGGTTTCGCCATGTTGGCCAGGCTGGTCTTGAACTCCTGA T C RSL1D1 Ensembl:ENSG00000171490 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1462927809 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51417,RMVar_hsa_circ_273603,RMVar_hsa_circ_326366,RMVar_hsa_circ_176325,RMVar_hsa_circ_341317 17503 RMVar_ID_17503 Human_SNP_ID_594717014 A-to-I Human chr16 - 11848635 11848635 11848635 ACAAAAATTAGCTGGGCCTACACCCAACTGGTACGTGCCTGGAGTCTCAGCTATGCTGGAGGCTA ACAAAAATTAGCTGGGCCTACACCCAACTGGTGCGTGCCTGGAGTCTCAGCTATGCTGGAGGCTA T C RSL1D1 Ensembl:ENSG00000171490 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1309082650 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51417,RMVar_hsa_circ_273603,RMVar_hsa_circ_326366,RMVar_hsa_circ_176325,RMVar_hsa_circ_341317 17504 RMVar_ID_17504 Human_SNP_ID_594717207 A-to-I Human chr16 - 11849239 11849221 11849239 AGCTGGGACTACAGGTGCACACCACCATGCCTAGCTAATTTTGAAATCTTTGTGGAGATGAGGTT AGCTGGGACTACAGGTGCACACCACCATGCCT__________________TGTGGAGATGAGGTT AAAGATTTCAAAATTAGCT A RSL1D1 Ensembl:ENSG00000171490 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs993676529 Functional Loss DEL dbSNP153 33..50 33 - - - RMVar_hsa_circ_51417,RMVar_hsa_circ_273603,RMVar_hsa_circ_326366,RMVar_hsa_circ_176325,RMVar_hsa_circ_341317 17505 RMVar_ID_17505 Human_SNP_ID_594717217 A-to-I Human chr16 - 11849261 11849261 11849261 CTCCCACCTCAGCCTTCCAAGTAGCTGGGACTACAGGTGCACACCACCATGCCTAGCTAATTTTG CTCCCACCTCAGCCTTCCAAGTAGCTGGGACTGCAGGTGCACACCACCATGCCTAGCTAATTTTG T C RSL1D1 Ensembl:ENSG00000171490 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs189542689 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1678623 RMVar_hsa_circ_51417,RMVar_hsa_circ_273603,RMVar_hsa_circ_326366,RMVar_hsa_circ_176325,RMVar_hsa_circ_341317 17506 RMVar_ID_17506 Human_SNP_ID_594718449 A-to-I Human chr16 + 11852275 11852275 11852275 CGGCGTGGTGGTGCGCGCCTGTAGTCCCGGCTACTTGGGAGGCGGAGGATGGAGGATCTTGAGGA CGGCGTGGTGGTGCGCGCCTGTAGTCCCGGCTGCTTGGGAGGCGGAGGATGGAGGATCTTGAGGA A G AC007216.4 Ensembl:ENSG00000263307 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs547216407 Functional Loss SNV dbSNP153 33..33 33 - - - 17507 RMVar_ID_17507 Human_SNP_ID_594718741 A-to-I Human chr16 + 11853063 11853063 11853063 ATGATCCACCTGCCTCGGCCTCCCAAAGTGCTAGGATTATAGGCGTGAACCACCACGGCCAATTT ATGATCCACCTGCCTCGGCCTCCCAAAGTGCTGGGATTATAGGCGTGAACCACCACGGCCAATTT A G AC007216.4 Ensembl:ENSG00000263307 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1052979730 Functional Loss SNV dbSNP153 33..33 33 - - - 17508 RMVar_ID_17508 Human_SNP_ID_594720021 A-to-I Human chr16 + 11856876 11856872 11856876 TTTTATTTATTTTAGTTTTGGGACAAGGTCTCACTCTGTCGCGCAGGCTGGAGTGTGGTGGGGTG TTTTATTTATTTTAGTTTTGGGACAAGGT____CTCTGTCGCGCAGGCTGGAGTGTGGTGGGGTG TCTCA T AC007216.4 Ensembl:ENSG00000263307 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1168829641 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_3511540 17509 RMVar_ID_17509 Human_SNP_ID_594724763 A-to-I Human chr16 - 11873835 11873835 11873835 CCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGCGGATCACCTGAGGCCAAGAGTTCAAGACC CCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGGATCACCTGAGGCCAAGAGTTCAAGACC T C GSPT1 Ensembl:ENSG00000103342 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1177787860 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265911 17510 RMVar_ID_17510 Human_SNP_ID_594727318 A-to-I Human chr16 - 11882772 11882772 11882772 TTTTTAAATAAAAATTGAGATGGGGTCTCACTATGTTGACCAGACTAGTCTCTAACTCCTGGCCT TTTTTAAATAAAAATTGAGATGGGGTCTCACTGTGTTGACCAGACTAGTCTCTAACTCCTGGCCT T C GSPT1 Ensembl:ENSG00000103342 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs917601479 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22935738 RMVar_hsa_circ_29325,RMVar_hsa_circ_265911,RMVar_hsa_circ_176334,RMVar_hsa_circ_290007,RMVar_hsa_circ_299414,RMVar_hsa_circ_328182,RMVar_hsa_circ_346910,RMVar_hsa_circ_335600,RMVar_hsa_circ_317023,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 17511 RMVar_ID_17511 Human_SNP_ID_594730184 A-to-I Human chr16 - 11891903 11891903 11891903 TATTCCCAGCACTTTGGGAGGCTGAGGCTGGCAGATCACTTGAGGTCAGGAGTTCGAGACCAGCC TATTCCCAGCACTTTGGGAGGCTGAGGCTGGCGGATCACTTGAGGTCAGGAGTTCGAGACCAGCC T C GSPT1 Ensembl:ENSG00000103342 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1333422268 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265911,RMVar_hsa_circ_290007,RMVar_hsa_circ_299414,RMVar_hsa_circ_346910,RMVar_hsa_circ_57970,RMVar_hsa_circ_176336,RMVar_hsa_circ_267294,RMVar_hsa_circ_378391,RMVar_hsa_circ_33614,RMVar_hsa_circ_44188,RMVar_hsa_circ_123824,RMVar_hsa_circ_122966,RMVar_hsa_circ_301376,RMVar_hsa_circ_296866,RMVar_hsa_circ_59894,RMVar_hsa_circ_176338,RMVar_hsa_circ_176339,RMVar_hsa_circ_176337,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_369412,RMVar_hsa_circ_322195,RMVar_hsa_circ_176348,RMVar_hsa_circ_176349,RMVar_hsa_circ_118833,RMVar_hsa_circ_176350,RMVar_hsa_circ_375603,RMVar_hsa_circ_176353,RMVar_hsa_circ_55711,RMVar_hsa_circ_124627,RMVar_hsa_circ_176352,RMVar_hsa_circ_352421,RMVar_hsa_circ_117900,RMVar_hsa_circ_176354 17512 RMVar_ID_17512 Human_SNP_ID_594730276 A-to-I Human chr16 - 11892227 11892227 11892227 GTGATCCTCTCACTTCAGCCTCCCAAGTAGCTAGGAATACAGGCATGCATCACCACACCAGGCCA GTGATCCTCTCACTTCAGCCTCCCAAGTAGCTGGGAATACAGGCATGCATCACCACACCAGGCCA T C GSPT1 Ensembl:ENSG00000103342 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1189655440 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265911,RMVar_hsa_circ_290007,RMVar_hsa_circ_299414,RMVar_hsa_circ_346910,RMVar_hsa_circ_57970,RMVar_hsa_circ_176336,RMVar_hsa_circ_267294,RMVar_hsa_circ_378391,RMVar_hsa_circ_33614,RMVar_hsa_circ_44188,RMVar_hsa_circ_123824,RMVar_hsa_circ_122966,RMVar_hsa_circ_301376,RMVar_hsa_circ_296866,RMVar_hsa_circ_59894,RMVar_hsa_circ_176338,RMVar_hsa_circ_176339,RMVar_hsa_circ_176337,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_369412,RMVar_hsa_circ_322195,RMVar_hsa_circ_176348,RMVar_hsa_circ_176349,RMVar_hsa_circ_118833,RMVar_hsa_circ_176350,RMVar_hsa_circ_375603,RMVar_hsa_circ_176353,RMVar_hsa_circ_55711,RMVar_hsa_circ_124627,RMVar_hsa_circ_176352,RMVar_hsa_circ_352421,RMVar_hsa_circ_117900,RMVar_hsa_circ_176354 17513 RMVar_ID_17513 Human_SNP_ID_594730303 A-to-I Human chr16 - 11892312 11892312 11892312 TAGAGACAGGGTCTTGCTCTTAAACACAGGCTAGAGTGCAGTGGTGGAATCATAGCTTACTGTAA TAGAGACAGGGTCTTGCTCTTAAACACAGGCTGGAGTGCAGTGGTGGAATCATAGCTTACTGTAA T C GSPT1 Ensembl:ENSG00000103342 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs933375570 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265911,RMVar_hsa_circ_290007,RMVar_hsa_circ_299414,RMVar_hsa_circ_346910,RMVar_hsa_circ_57970,RMVar_hsa_circ_176336,RMVar_hsa_circ_267294,RMVar_hsa_circ_378391,RMVar_hsa_circ_33614,RMVar_hsa_circ_44188,RMVar_hsa_circ_123824,RMVar_hsa_circ_122966,RMVar_hsa_circ_301376,RMVar_hsa_circ_296866,RMVar_hsa_circ_59894,RMVar_hsa_circ_176338,RMVar_hsa_circ_176339,RMVar_hsa_circ_176337,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_369412,RMVar_hsa_circ_322195,RMVar_hsa_circ_176348,RMVar_hsa_circ_176349,RMVar_hsa_circ_118833,RMVar_hsa_circ_176350,RMVar_hsa_circ_375603,RMVar_hsa_circ_176353,RMVar_hsa_circ_55711,RMVar_hsa_circ_124627,RMVar_hsa_circ_176352,RMVar_hsa_circ_352421,RMVar_hsa_circ_117900,RMVar_hsa_circ_176354 17514 RMVar_ID_17514 Human_SNP_ID_594730764 A-to-I Human chr16 - 11893160 11893160 11893160 AAATTCCTGTGCTCAACTGATCCTCCTACCTCAGCCTCCCAAGTAGCTGGGACTACACGCTTGCA AAATTCCTGTGCTCAACTGATCCTCCTACCTCCGCCTCCCAAGTAGCTGGGACTACACGCTTGCA T G GSPT1 Ensembl:ENSG00000103342 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs919230986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17563975 RMVar_hsa_circ_265911,RMVar_hsa_circ_290007,RMVar_hsa_circ_299414,RMVar_hsa_circ_346910,RMVar_hsa_circ_57970,RMVar_hsa_circ_176336,RMVar_hsa_circ_267294,RMVar_hsa_circ_378391,RMVar_hsa_circ_33614,RMVar_hsa_circ_44188,RMVar_hsa_circ_123824,RMVar_hsa_circ_122966,RMVar_hsa_circ_301376,RMVar_hsa_circ_296866,RMVar_hsa_circ_59894,RMVar_hsa_circ_176338,RMVar_hsa_circ_176339,RMVar_hsa_circ_176337,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_369412,RMVar_hsa_circ_322195,RMVar_hsa_circ_176348,RMVar_hsa_circ_176349,RMVar_hsa_circ_118833,RMVar_hsa_circ_176350,RMVar_hsa_circ_375603,RMVar_hsa_circ_176353,RMVar_hsa_circ_55711,RMVar_hsa_circ_124627,RMVar_hsa_circ_176352,RMVar_hsa_circ_352421,RMVar_hsa_circ_117900,RMVar_hsa_circ_176354 17515 RMVar_ID_17515 Human_SNP_ID_594731256 A-to-I Human chr16 - 11894765 11894765 11894765 TGATTTTTGGCCTGGTGTGGTGGAACACACCTATAATCCCAGCATTTTGAGAGGCTAAGGTGGGA TGATTTTTGGCCTGGTGTGGTGGAACACACCTGTAATCCCAGCATTTTGAGAGGCTAAGGTGGGA T C GSPT1 Ensembl:ENSG00000103342 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1240225908 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265911,RMVar_hsa_circ_290007,RMVar_hsa_circ_299414,RMVar_hsa_circ_346910,RMVar_hsa_circ_57970,RMVar_hsa_circ_176336,RMVar_hsa_circ_267294,RMVar_hsa_circ_378391,RMVar_hsa_circ_33614,RMVar_hsa_circ_44188,RMVar_hsa_circ_123824,RMVar_hsa_circ_122966,RMVar_hsa_circ_301376,RMVar_hsa_circ_296866,RMVar_hsa_circ_59894,RMVar_hsa_circ_176338,RMVar_hsa_circ_176339,RMVar_hsa_circ_176337,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_369412,RMVar_hsa_circ_322195,RMVar_hsa_circ_176348,RMVar_hsa_circ_176349,RMVar_hsa_circ_118833,RMVar_hsa_circ_176350,RMVar_hsa_circ_375603,RMVar_hsa_circ_176353,RMVar_hsa_circ_55711,RMVar_hsa_circ_124627,RMVar_hsa_circ_176352,RMVar_hsa_circ_352421,RMVar_hsa_circ_117900,RMVar_hsa_circ_176354 17516 RMVar_ID_17516 Human_SNP_ID_594731361 A-to-I Human chr16 - 11895174 11895174 11895174 CGCCCTCGCTGGCCTCCCAAAGTGCTGGAATTACAGGCGTGAGCCACCGAGCCCAGCCTTGAGGC CGCCCTCGCTGGCCTCCCAAAGTGCTGGAATTGCAGGCGTGAGCCACCGAGCCCAGCCTTGAGGC T C GSPT1 Ensembl:ENSG00000103342 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256569964 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23162942 RMVar_hsa_circ_265911,RMVar_hsa_circ_290007,RMVar_hsa_circ_299414,RMVar_hsa_circ_346910,RMVar_hsa_circ_176336,RMVar_hsa_circ_378391,RMVar_hsa_circ_33614,RMVar_hsa_circ_44188,RMVar_hsa_circ_123824,RMVar_hsa_circ_301376,RMVar_hsa_circ_296866,RMVar_hsa_circ_59894,RMVar_hsa_circ_176338,RMVar_hsa_circ_176337,RMVar_hsa_circ_288012,RMVar_hsa_circ_176343,RMVar_hsa_circ_120157,RMVar_hsa_circ_176344,RMVar_hsa_circ_176345,RMVar_hsa_circ_102019,RMVar_hsa_circ_322195,RMVar_hsa_circ_176349,RMVar_hsa_circ_118833,RMVar_hsa_circ_176350,RMVar_hsa_circ_375603,RMVar_hsa_circ_55711,RMVar_hsa_circ_124627,RMVar_hsa_circ_176352,RMVar_hsa_circ_352421,RMVar_hsa_circ_176354,RMVar_hsa_circ_176356,RMVar_hsa_circ_176358,RMVar_hsa_circ_280014,RMVar_hsa_circ_302457,RMVar_hsa_circ_328991,RMVar_hsa_circ_81081,RMVar_hsa_circ_176357,RMVar_hsa_circ_176355 17517 RMVar_ID_17517 Human_SNP_ID_594731428 A-to-I Human chr16 - 11895392 11895392 11895392 AGTTTCACTCTTGTCGCCCAGGCTGGAGTGCAATGGCGTGATTTCAGCTTAGTGCAACCTCTGCT AGTTTCACTCTTGTCGCCCAGGCTGGAGTGCAGTGGCGTGATTTCAGCTTAGTGCAACCTCTGCT T C GSPT1 Ensembl:ENSG00000103342 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs556508530 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265911,RMVar_hsa_circ_290007,RMVar_hsa_circ_299414,RMVar_hsa_circ_346910,RMVar_hsa_circ_176336,RMVar_hsa_circ_378391,RMVar_hsa_circ_33614,RMVar_hsa_circ_44188,RMVar_hsa_circ_123824,RMVar_hsa_circ_301376,RMVar_hsa_circ_296866,RMVar_hsa_circ_59894,RMVar_hsa_circ_176338,RMVar_hsa_circ_176337,RMVar_hsa_circ_288012,RMVar_hsa_circ_176343,RMVar_hsa_circ_120157,RMVar_hsa_circ_176344,RMVar_hsa_circ_176345,RMVar_hsa_circ_102019,RMVar_hsa_circ_322195,RMVar_hsa_circ_176349,RMVar_hsa_circ_118833,RMVar_hsa_circ_176350,RMVar_hsa_circ_375603,RMVar_hsa_circ_55711,RMVar_hsa_circ_124627,RMVar_hsa_circ_176352,RMVar_hsa_circ_352421,RMVar_hsa_circ_176354,RMVar_hsa_circ_176356,RMVar_hsa_circ_176358,RMVar_hsa_circ_280014,RMVar_hsa_circ_302457,RMVar_hsa_circ_328991,RMVar_hsa_circ_81081,RMVar_hsa_circ_176357,RMVar_hsa_circ_176355 17518 RMVar_ID_17518 Human_SNP_ID_594732867 A-to-I Human chr16 - 11900162 11900160 11900162 CCAGCTAATTGTTTTGTATTTTCAGTAGAGACAGGGTTTTGCCATGTTGGCCGGGTTGGTCTTGA CCAGCTAATTGTTTTGTATTTTCAGTAGAGAC__GGTTTTGCCATGTTGGCCGGGTTGGTCTTGA CCT C GSPT1 Ensembl:ENSG00000103342 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs890529147 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_12666693 RMVar_hsa_circ_123824,RMVar_hsa_circ_176345,RMVar_hsa_circ_102019,RMVar_hsa_circ_176349,RMVar_hsa_circ_176358,RMVar_hsa_circ_81081 17519 RMVar_ID_17519 Human_SNP_ID_594733156 A-to-I Human chr16 - 11901151 11901149 11901151 AATATATCGGTTTTATTTTTATTTTTTGAGACAGGGTGTCACTCTCTCGCCCAGGCTGGAGTGCA AATATATCGGTTTTATTTTTATTTTTTGAGAC__GGTGTCACTCTCTCGCCCAGGCTGGAGTGCA CCT C GSPT1 Ensembl:ENSG00000103342 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1177544271 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_2468102,Human_RBP_ID_12666747 RMVar_hsa_circ_123824,RMVar_hsa_circ_176345,RMVar_hsa_circ_102019,RMVar_hsa_circ_176349,RMVar_hsa_circ_176358,RMVar_hsa_circ_81081 17520 RMVar_ID_17520 Human_SNP_ID_594733398 A-to-I Human chr16 - 11902042 11902042 11902042 TCTTGTTGCCCAGGCTGGAGTGCGATGGTGCAATCTCAGCTCACTGCAACCTCTGCCTCCCGGGT TCTTGTTGCCCAGGCTGGAGTGCGATGGTGCAGTCTCAGCTCACTGCAACCTCTGCCTCCCGGGT T C GSPT1 Ensembl:ENSG00000103342 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs905669498 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123824,RMVar_hsa_circ_176345,RMVar_hsa_circ_102019,RMVar_hsa_circ_176349,RMVar_hsa_circ_176358,RMVar_hsa_circ_81081 17521 RMVar_ID_17521 Human_SNP_ID_594734175 A-to-I Human chr16 - 11904341 11904341 11904341 AAAATTACCCAGGCGTGGTGGCGCGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGGGA AAAATTACCCAGGCGTGGTGGCGCGCGCCTGTTGTCCCAGCTACTCGGGAGGCTGAGGCAGGGGA T A GSPT1 Ensembl:ENSG00000103342 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956745857 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_126503 RMVar_hsa_circ_123824,RMVar_hsa_circ_176345,RMVar_hsa_circ_102019,RMVar_hsa_circ_176349,RMVar_hsa_circ_176358,RMVar_hsa_circ_81081 17522 RMVar_ID_17522 Human_SNP_ID_594734414 A-to-I Human chr16 - 11905054 11905054 11905054 TGTTTTGTTGTTATTGTTTGATACAGGGTCTTACTCTGTCACCCAGGCTGGAGTGCAGTGGTGTG TGTTTTGTTGTTATTGTTTGATACAGGGTCTTGCTCTGTCACCCAGGCTGGAGTGCAGTGGTGTG T C GSPT1 Ensembl:ENSG00000103342 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1014403919 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1838099,Human_RBP_ID_24369818 RMVar_hsa_circ_123824,RMVar_hsa_circ_176345,RMVar_hsa_circ_102019,RMVar_hsa_circ_176349,RMVar_hsa_circ_176358,RMVar_hsa_circ_81081 17523 RMVar_ID_17523 Human_SNP_ID_594735925 A-to-I Human chr16 - 11909982 11909982 11909982 AGTGATCTTTCACCTCAGCTTCCTGAGTAGCTAGGACTATAGGCACCCACCATGACGCCTGGCTA AGTGATCTTTCACCTCAGCTTCCTGAGTAGCTGGGACTATAGGCACCCACCATGACGCCTGGCTA T C GSPT1 Ensembl:ENSG00000103342 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs948817305 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12667210 RMVar_hsa_circ_123824,RMVar_hsa_circ_176345,RMVar_hsa_circ_102019,RMVar_hsa_circ_176349,RMVar_hsa_circ_176358,RMVar_hsa_circ_81081 17524 RMVar_ID_17524 Human_SNP_ID_594735945 A-to-I Human chr16 - 11910061 11910061 11910061 ACGGGATCTTACTTTGTCACCCAAGCTGGAGTATAATTGTGTGATTATAGCTCATCGTAACTTCA ACGGGATCTTACTTTGTCACCCAAGCTGGAGTGTAATTGTGTGATTATAGCTCATCGTAACTTCA T C GSPT1 Ensembl:ENSG00000103342 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs954437647 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9819423,Human_RBP_ID_12667210 RMVar_hsa_circ_123824,RMVar_hsa_circ_176345,RMVar_hsa_circ_102019,RMVar_hsa_circ_176349,RMVar_hsa_circ_176358,RMVar_hsa_circ_81081 17525 RMVar_ID_17525 Human_SNP_ID_594736677 A-to-I Human chr16 - 11912285 11912285 11912285 GGAGTGCAATGGCACGATCTCGGCTGACTACAACCTCCTCCTCCCAGGTTCAAGCAATTCTCCTG GGAGTGCAATGGCACGATCTCGGCTGACTACAGCCTCCTCCTCCCAGGTTCAAGCAATTCTCCTG T C GSPT1 Ensembl:ENSG00000103342 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027272132 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12667360 RMVar_hsa_circ_123824,RMVar_hsa_circ_176345,RMVar_hsa_circ_102019,RMVar_hsa_circ_176349,RMVar_hsa_circ_176358,RMVar_hsa_circ_81081 17526 RMVar_ID_17526 Human_SNP_ID_594760707 A-to-I Human chr16 + 11984119 11984119 11984119 TCACACCTGTAATTCCAGCACTTTAGGAGGCTAAGGTGGGAGGATCGCTTGAGCCCAGGAGTTTG TCACACCTGTAATTCCAGCACTTTAGGAGGCTGAGGTGGGAGGATCGCTTGAGCCCAGGAGTTTG A G SNX29 Ensembl:ENSG00000048471 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs939184095 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_176363,RMVar_hsa_circ_127833,RMVar_hsa_circ_176364,RMVar_hsa_circ_176365 17527 RMVar_ID_17527 Human_SNP_ID_594760708 A-to-I Human chr16 + 11984119 11984119 11984119 TCACACCTGTAATTCCAGCACTTTAGGAGGCTAAGGTGGGAGGATCGCTTGAGCCCAGGAGTTTG TCACACCTGTAATTCCAGCACTTTAGGAGGCTTAGGTGGGAGGATCGCTTGAGCCCAGGAGTTTG A T SNX29 Ensembl:ENSG00000048471 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs939184095 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_176363,RMVar_hsa_circ_127833,RMVar_hsa_circ_176364,RMVar_hsa_circ_176365 17528 RMVar_ID_17528 Human_SNP_ID_594760737 A-to-I Human chr16 + 11984224 11984224 11984224 TTTGTACACACACACACAAATTAGCTGGATGTAGTGGTGCATGCCCATGGTCCTAGCCACTCGAG TTTGTACACACACACACAAATTAGCTGGATGTGGTGGTGCATGCCCATGGTCCTAGCCACTCGAG A G SNX29 Ensembl:ENSG00000048471 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1009807885 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_176363,RMVar_hsa_circ_127833,RMVar_hsa_circ_176364,RMVar_hsa_circ_176365 17529 RMVar_ID_17529 Human_SNP_ID_594792905 A-to-I Human chr16 + 12084959 12084959 12084959 GGATATGGTGGTGCGTACCTGTATTCCCAGCTAATTGGGAGGCTGAGGCAGGAGGATTCTTTGAG GGATATGGTGGTGCGTACCTGTATTCCCAGCTTATTGGGAGGCTGAGGCAGGAGGATTCTTTGAG A T SNX29 Ensembl:ENSG00000048471 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs529544752 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_176363,RMVar_hsa_circ_127833,RMVar_hsa_circ_74057,RMVar_hsa_circ_100866,RMVar_hsa_circ_32289,RMVar_hsa_circ_306268,RMVar_hsa_circ_176372,RMVar_hsa_circ_316771,RMVar_hsa_circ_283436,RMVar_hsa_circ_128171,RMVar_hsa_circ_176376,RMVar_hsa_circ_114174,RMVar_hsa_circ_32532,RMVar_hsa_circ_176379 17530 RMVar_ID_17530 Human_SNP_ID_594806582 A-to-I Human chr16 + 12127539 12127539 12127539 CACCTCCCGGGCTCAAGTGATCCTCCAGCGTCAGCCTTCTGAGTGGCTGAGACTACAGGCGCATG CACCTCCCGGGCTCAAGTGATCCTCCAGCGTCCGCCTTCTGAGTGGCTGAGACTACAGGCGCATG A C SNX29 Ensembl:ENSG00000048471 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs909578697 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_176363,RMVar_hsa_circ_127833,RMVar_hsa_circ_74057,RMVar_hsa_circ_100866,RMVar_hsa_circ_32289,RMVar_hsa_circ_306268,RMVar_hsa_circ_176372,RMVar_hsa_circ_316771,RMVar_hsa_circ_283436,RMVar_hsa_circ_128171,RMVar_hsa_circ_176376,RMVar_hsa_circ_114174,RMVar_hsa_circ_5008,RMVar_hsa_circ_363050,RMVar_hsa_circ_32532,RMVar_hsa_circ_176379,RMVar_hsa_circ_374042,RMVar_hsa_circ_88873,RMVar_hsa_circ_30654,RMVar_hsa_circ_176382,RMVar_hsa_circ_176383 17531 RMVar_ID_17531 Human_SNP_ID_594808086 A-to-I Human chr16 + 12132198 12132198 12132198 TCGGCTCACTGCAACCTCTGCCTCCCGGGTTCAGGTGATTCTCCGGCCTCAACCTCCCAAGTAGC TCGGCTCACTGCAACCTCTGCCTCCCGGGTTCGGGTGATTCTCCGGCCTCAACCTCCCAAGTAGC A G SNX29 Ensembl:ENSG00000048471 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1182855470 Functional Loss SNV dbSNP153 33..33 33 - - - 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 17532 RMVar_ID_17532 Human_SNP_ID_594827792 A-to-I Human chr16 + 12193394 12193394 12193394 TGGGATCTGAGGCAGGAGAATCACTTGAAGCCAGGAGGTGAAGGTTGTAGTGAGCCGAGATCGCA TGGGATCTGAGGCAGGAGAATCACTTGAAGCCGGGAGGTGAAGGTTGTAGTGAGCCGAGATCGCA A G SNX29 Ensembl:ENSG00000048471 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978149202 Functional Loss SNV dbSNP153 33..33 33 - - - 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 17533 RMVar_ID_17533 Human_SNP_ID_594857894 A-to-I Human chr16 + 12280939 12280939 12280939 ATTTATTTAGTTATTTATGGAGACAGGGTCTCAGTCTGTCGCCTAGGCTGGAGTGCAGTGGTACA ATTTATTTAGTTATTTATGGAGACAGGGTCTCTGTCTGTCGCCTAGGCTGGAGTGCAGTGGTACA A T SNX29 Ensembl:ENSG00000048471 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1475066463 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_176363,RMVar_hsa_circ_127833,RMVar_hsa_circ_100866,RMVar_hsa_circ_176372,RMVar_hsa_circ_128171,RMVar_hsa_circ_176376,RMVar_hsa_circ_114174,RMVar_hsa_circ_176379,RMVar_hsa_circ_88873,RMVar_hsa_circ_30654,RMVar_hsa_circ_176383,RMVar_hsa_circ_36467,RMVar_hsa_circ_356922 17534 RMVar_ID_17534 Human_SNP_ID_595126764 A-to-I Human chr16 + 12953986 12953986 12953986 AAACTGCCCCTAAGATCCAGTCACCTCCAACCAGGTCCCTGCCTCAACCTGTGGGGATTACAATT AAACTGCCCCTAAGATCCAGTCACCTCCAACCGGGTCCCTGCCTCAACCTGTGGGGATTACAATT A G SHISA9 Ensembl:ENSG00000237515 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank;ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1177880945 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119411,RMVar_hsa_circ_176393 17535 RMVar_ID_17535 Human_SNP_ID_595274024 A-to-I Human chr16 - 13458493 13458493 13458493 TCAGCCATTGTTGATCGAGTTTTTTCTAGATTACCAATTTCTAGCTGTAAATGAGTAATTTCCCC TCAGCCATTGTTGATCGAGTTTTTTCTAGATTGCCAATTTCTAGCTGTAAATGAGTAATTTCCCC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs547558581 Functional Loss SNV dbSNP153 33..33 33 - - - 17536 RMVar_ID_17536 Human_SNP_ID_595423246 A-to-I Human chr16 + 13948643 13948643 13948643 AGGTAAAGTTCCTACAAGTGATTACAGAAGGTAGAAACTTTACCTGATCCTAACAGATCTCATTT AGGTAAAGTTCCTACAAGTGATTACAGAAGGTGGAAACTTTACCTGATCCTAACAGATCTCATTT A G ERCC4 Ensembl:ENSG00000175595 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1177597738 Functional Loss SNV dbSNP153 33..33 33 - - - 17537 RMVar_ID_17537 Human_SNP_ID_595423250 A-to-I Human chr16 + 13948665 13948664 13948666 TACAGAAGGTAGAAACTTTACCTGATCCTAACAGATCTCATTTAGAAAGGAATATGCTAAGCCTG TACAGAAGGTAGAAACTTTACCTGATCCTAAC__ATCTCATTTAGAAAGGAATATGCTAAGCCTG CAG C ERCC4 Ensembl:ENSG00000175595 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1311057184 Functional Loss DEL dbSNP153 33..34 33 - - - 17538 RMVar_ID_17538 Human_SNP_ID_595423251 A-to-I Human chr16 + 13948665 13948665 13948665 TACAGAAGGTAGAAACTTTACCTGATCCTAACAGATCTCATTTAGAAAGGAATATGCTAAGCCTG TACAGAAGGTAGAAACTTTACCTGATCCTAACTGATCTCATTTAGAAAGGAATATGCTAAGCCTG A T ERCC4 Ensembl:ENSG00000175595 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs147799208 Functional Loss SNV dbSNP153 33..33 33 - - - 17539 RMVar_ID_17539 Human_SNP_ID_595423253 A-to-I Human chr16 + 13948672 13948672 13948672 GGTAGAAACTTTACCTGATCCTAACAGATCTCATTTAGAAAGGAATATGCTAAGCCTGGCATGGA GGTAGAAACTTTACCTGATCCTAACAGATCTCGTTTAGAAAGGAATATGCTAAGCCTGGCATGGA A G ERCC4 Ensembl:ENSG00000175595 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1005656572 Functional Loss SNV dbSNP153 33..33 33 - - - 17540 RMVar_ID_17540 Human_SNP_ID_595423258 A-to-I Human chr16 + 13948691 13948691 13948691 CCTAACAGATCTCATTTAGAAAGGAATATGCTAAGCCTGGCATGGACGGTGCAGGGAGGGAAAAG CCTAACAGATCTCATTTAGAAAGGAATATGCTCAGCCTGGCATGGACGGTGCAGGGAGGGAAAAG A C ERCC4 Ensembl:ENSG00000175595 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1474621617 Functional Loss SNV dbSNP153 33..33 33 - - - 17541 RMVar_ID_17541 Human_SNP_ID_595494213 A-to-I Human chr16 + 14231633 14231633 14231633 TCATTTAGCTCCCGCTTGTGAGAACATGCAGTATTTGGTTTTCTGTTCCTGCATTCGTTCACTAC TCATTTAGCTCCCGCTTGTGAGAACATGCAGTGTTTGGTTTTCTGTTCCTGCATTCGTTCACTAC A G MRTFB Ensembl:ENSG00000186260 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1451495263 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7677,RMVar_hsa_circ_125458,RMVar_hsa_circ_125973,RMVar_hsa_circ_176406,RMVar_hsa_circ_176405,RMVar_hsa_circ_32683,RMVar_hsa_circ_176411,RMVar_hsa_circ_266095,RMVar_hsa_circ_316647,RMVar_hsa_circ_176412 17542 RMVar_ID_17542 Human_SNP_ID_595520519 A-to-I Human chr16 + 14325447 14325447 14325447 TCGAGGCTACAGTGAGCTGTGATTGTACCGCTATACCCCAGCCTGGGTGACAAAGTAAGACCCTG TCGAGGCTACAGTGAGCTGTGATTGTACCGCTCTACCCCAGCCTGGGTGACAAAGTAAGACCCTG A C MIR193BHG Ensembl:ENSG00000262454 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs575849795 Functional Loss SNV dbSNP153 33..33 33 - - - 17543 RMVar_ID_17543 Human_SNP_ID_595520913 A-to-I Human chr16 + 14326917 14326917 14326917 TTTTTTTTTTTTTTGAGATGGAGTCTCGCTCTATTGTCCAGGTTGGAGTGCAGTGGTGCAATCTC TTTTTTTTTTTTTTGAGATGGAGTCTCGCTCTGTTGTCCAGGTTGGAGTGCAGTGGTGCAATCTC A G MIR193BHG Ensembl:ENSG00000262454 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417070912 Functional Loss SNV dbSNP153 33..33 33 - - - 17544 RMVar_ID_17544 Human_SNP_ID_595521077 A-to-I Human chr16 + 14327622 14327622 14327622 CCCTCCTTGACCTCCCAAAGTGTTGGGATTACAAGCATGAGCCACCGCACCCGGCCTACCTACAA CCCTCCTTGACCTCCCAAAGTGTTGGGATTACGAGCATGAGCCACCGCACCCGGCCTACCTACAA A G MIR193BHG Ensembl:ENSG00000262454 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs999981714 Functional Loss SNV dbSNP153 33..33 33 - - - 17545 RMVar_ID_17545 Human_SNP_ID_595521113 A-to-I Human chr16 + 14327716 14327716 14327716 TCTCCCAGGCTGGAGTGCAGTGGCGCGATCTCAGCTCACTGCAAGCTCTACATCCCGGGTTCATG TCTCCCAGGCTGGAGTGCAGTGGCGCGATCTCGGCTCACTGCAAGCTCTACATCCCGGGTTCATG A G MIR193BHG Ensembl:ENSG00000262454 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs201778077 Functional Loss SNV dbSNP153 33..33 33 - - - 17546 RMVar_ID_17546 Human_SNP_ID_595521584 A-to-I Human chr16 + 14329349 14329348 14329349 CGGAAGTTGCAGTGAGCCAAGATTGTGCCACTACACTCCAGCCTAGGTGACAGAGCAAGACGCCC CGGAAGTTGCAGTGAGCCAAGATTGTGCCACT_CACTCCAGCCTAGGTGACAGAGCAAGACGCCC TA T MIR193BHG Ensembl:ENSG00000262454 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1329258261 Functional Loss DEL dbSNP153 33..33 33 - - - 17547 RMVar_ID_17547 Human_SNP_ID_595521585 A-to-I Human chr16 + 14329349 14329349 14329349 CGGAAGTTGCAGTGAGCCAAGATTGTGCCACTACACTCCAGCCTAGGTGACAGAGCAAGACGCCC CGGAAGTTGCAGTGAGCCAAGATTGTGCCACTGCACTCCAGCCTAGGTGACAGAGCAAGACGCCC A G MIR193BHG Ensembl:ENSG00000262454 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1302137569 Functional Loss SNV dbSNP153 33..33 33 - - - 17548 RMVar_ID_17548 Human_SNP_ID_595521587 A-to-I Human chr16 + 14329361 14329361 14329361 TGAGCCAAGATTGTGCCACTACACTCCAGCCTAGGTGACAGAGCAAGACGCCCATCTCAAAAAAA TGAGCCAAGATTGTGCCACTACACTCCAGCCTCGGTGACAGAGCAAGACGCCCATCTCAAAAAAA A C MIR193BHG Ensembl:ENSG00000262454 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1012103463 Functional Loss SNV dbSNP153 33..33 33 - - - 17549 RMVar_ID_17549 Human_SNP_ID_595521588 A-to-I Human chr16 + 14329361 14329361 14329361 TGAGCCAAGATTGTGCCACTACACTCCAGCCTAGGTGACAGAGCAAGACGCCCATCTCAAAAAAA TGAGCCAAGATTGTGCCACTACACTCCAGCCTGGGTGACAGAGCAAGACGCCCATCTCAAAAAAA A G MIR193BHG Ensembl:ENSG00000262454 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1012103463 Functional Loss SNV dbSNP153 33..33 33 - - - 17550 RMVar_ID_17550 Human_SNP_ID_595522000 A-to-I Human chr16 + 14330679 14330679 14330679 CCAGGAGTCAGAGGTTGCAGCGAGCTGATATCATGCCACCGCACTCTAGCCTGGGCAACAGAGCA CCAGGAGTCAGAGGTTGCAGCGAGCTGATATCGTGCCACCGCACTCTAGCCTGGGCAACAGAGCA A G MIR193BHG Ensembl:ENSG00000262454 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1262548232 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25191857 17551 RMVar_ID_17551 Human_SNP_ID_595559037 A-to-I Human chr16 - 14470701 14470701 14470701 TAATCCCAGCCCTTTGGAATGCTGAGATGGGCAGATCACTTGGGCTCAGGAGTTCAAGAGCAGCC TAATCCCAGCCCTTTGGAATGCTGAGATGGGCTGATCACTTGGGCTCAGGAGTTCAAGAGCAGCC T A PARN Ensembl:ENSG00000140694 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264050619 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81827,RMVar_hsa_circ_176421 17552 RMVar_ID_17552 Human_SNP_ID_595578922 A-to-I Human chr16 - 14551421 14551421 14551421 GGGATTACAGGCGCGCAACATGATACCCGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCA GGGATTACAGGCGCGCAACATGATACCCGGCTGATTTTTGTATTTTTAGTAGAGATGGGGTTTCA T C PARN Ensembl:ENSG00000140694 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1344606878 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 17553 RMVar_ID_17553 Human_SNP_ID_595583509 A-to-I Human chr16 - 14568832 14568832 14568832 AGAGTGCAATGGCGTGATCTCGGCTCACTGCAACCTCTGCCTCCCAGGTTCAAGCGATTCCCCTT AGAGTGCAATGGCGTGATCTCGGCTCACTGCACCCTCTGCCTCCCAGGTTCAAGCGATTCCCCTT T G PARN Ensembl:ENSG00000140694 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1441602255 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69205,RMVar_hsa_circ_81827,RMVar_hsa_circ_176421,RMVar_hsa_circ_68448,RMVar_hsa_circ_312391,RMVar_hsa_circ_370332,RMVar_hsa_circ_370001,RMVar_hsa_circ_317954,RMVar_hsa_circ_308960,RMVar_hsa_circ_266852,RMVar_hsa_circ_176425,RMVar_hsa_circ_176427,RMVar_hsa_circ_176428,RMVar_hsa_circ_176426,RMVar_hsa_circ_176424,RMVar_hsa_circ_377783 17554 RMVar_ID_17554 Human_SNP_ID_595597526 A-to-I Human chr16 - 14618092 14618092 14618092 GTCTCGAACTTCTGACCTCAAGTGATGTGCCCACCTCTGCCTCCCAAAGTGCTGGGATTACAGGC GTCTCGAACTTCTGACCTCAAGTGATGTGCCCTCCTCTGCCTCCCAAAGTGCTGGGATTACAGGC T A PARN Ensembl:ENSG00000140694 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs932836635 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17563985 RMVar_hsa_circ_69205,RMVar_hsa_circ_287840,RMVar_hsa_circ_176435,RMVar_hsa_circ_176436,RMVar_hsa_circ_119671,RMVar_hsa_circ_275170,RMVar_hsa_circ_176445,RMVar_hsa_circ_176444,RMVar_hsa_circ_108695,RMVar_hsa_circ_176449,RMVar_hsa_circ_66654,RMVar_hsa_circ_319240,RMVar_hsa_circ_176450,RMVar_hsa_circ_304624,RMVar_hsa_circ_43029,RMVar_hsa_circ_176453,RMVar_hsa_circ_334549,RMVar_hsa_circ_34997,RMVar_hsa_circ_98202,RMVar_hsa_circ_176454,RMVar_hsa_circ_176455,RMVar_hsa_circ_176456 17555 RMVar_ID_17555 Human_SNP_ID_595599692 A-to-I Human chr16 - 14625453 14625453 14625453 CGCTCTTCTTGTCCAGGCTAGAGTGTGATGGCATGATCTAGGCTCACTGTAACCTCTGCCTCCTG CGCTCTTCTTGTCCAGGCTAGAGTGTGATGGCGTGATCTAGGCTCACTGTAACCTCTGCCTCCTG T C PARN Ensembl:ENSG00000140694 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs558411738 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69205,RMVar_hsa_circ_287840,RMVar_hsa_circ_176435,RMVar_hsa_circ_176436,RMVar_hsa_circ_119671,RMVar_hsa_circ_275170,RMVar_hsa_circ_176445,RMVar_hsa_circ_176444,RMVar_hsa_circ_108695,RMVar_hsa_circ_176449,RMVar_hsa_circ_66654,RMVar_hsa_circ_319240,RMVar_hsa_circ_176450,RMVar_hsa_circ_304624,RMVar_hsa_circ_43029,RMVar_hsa_circ_176453,RMVar_hsa_circ_334549,RMVar_hsa_circ_34997,RMVar_hsa_circ_98202,RMVar_hsa_circ_176454,RMVar_hsa_circ_176455,RMVar_hsa_circ_176456 17556 RMVar_ID_17556 Human_SNP_ID_595600065 A-to-I Human chr16 - 14626750 14626750 14626750 AAATTTGCCGAGTGTGGTCATGGGTGCCTGTAATCCCAGCTACTTAGGGAGGCTGAGGCAGGAGA AAATTTGCCGAGTGTGGTCATGGGTGCCTGTAGTCCCAGCTACTTAGGGAGGCTGAGGCAGGAGA T C PARN Ensembl:ENSG00000140694 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1347953383 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69205,RMVar_hsa_circ_287840,RMVar_hsa_circ_176435,RMVar_hsa_circ_176436,RMVar_hsa_circ_119671,RMVar_hsa_circ_275170,RMVar_hsa_circ_176445,RMVar_hsa_circ_176444,RMVar_hsa_circ_108695,RMVar_hsa_circ_176449,RMVar_hsa_circ_66654,RMVar_hsa_circ_319240,RMVar_hsa_circ_176450,RMVar_hsa_circ_304624,RMVar_hsa_circ_43029,RMVar_hsa_circ_176453,RMVar_hsa_circ_334549,RMVar_hsa_circ_34997,RMVar_hsa_circ_98202,RMVar_hsa_circ_176454,RMVar_hsa_circ_176455,RMVar_hsa_circ_176456 17557 RMVar_ID_17557 Human_SNP_ID_595604053 A-to-I Human chr16 + 14639415 14639415 14639415 CTGCATCCTCCACGTCCTGGGTGCAAATGATTATCCTGCCTCAACCTCCTGAGTAGCTGGGATTA CTGCATCCTCCACGTCCTGGGTGCAAATGATTCTCCTGCCTCAACCTCCTGAGTAGCTGGGATTA A C BFAR Ensembl:ENSG00000103429 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs534386661 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_176459,RMVar_hsa_circ_97603 17558 RMVar_ID_17558 Human_SNP_ID_595604054 A-to-I Human chr16 + 14639415 14639415 14639415 CTGCATCCTCCACGTCCTGGGTGCAAATGATTATCCTGCCTCAACCTCCTGAGTAGCTGGGATTA CTGCATCCTCCACGTCCTGGGTGCAAATGATTGTCCTGCCTCAACCTCCTGAGTAGCTGGGATTA A G BFAR Ensembl:ENSG00000103429 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs534386661 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_176459,RMVar_hsa_circ_97603 17559 RMVar_ID_17559 Human_SNP_ID_595604200 A-to-I Human chr16 + 14639975 14639975 14639975 GAGTTTAGGAGTTCGAGATCAGCCTGGGCAACATGGCAAAATCCCATCTCTGCAGAAAATTAGCC GAGTTTAGGAGTTCGAGATCAGCCTGGGCAACGTGGCAAAATCCCATCTCTGCAGAAAATTAGCC A G BFAR Ensembl:ENSG00000103429 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs892443488 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_176459,RMVar_hsa_circ_97603 17560 RMVar_ID_17560 Human_SNP_ID_595605737 A-to-I Human chr16 + 14645192 14645192 14645192 TAAAAATTAGCCAGGTGTGGTGGTACATGCCTATAGTCCCAGCTATGCCAGTGGCTGAGGTGGGA TAAAAATTAGCCAGGTGTGGTGGTACATGCCTGTAGTCCCAGCTATGCCAGTGGCTGAGGTGGGA A G BFAR Ensembl:ENSG00000103429 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1307324585 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25192505 RMVar_hsa_circ_176462,RMVar_hsa_circ_300697,RMVar_hsa_circ_373028,RMVar_hsa_circ_377710,RMVar_hsa_circ_303805,RMVar_hsa_circ_79532,RMVar_hsa_circ_176464,RMVar_hsa_circ_176463,RMVar_hsa_circ_176460,RMVar_hsa_circ_176461 17561 RMVar_ID_17561 Human_SNP_ID_595606320 A-to-I Human chr16 + 14647346 14647346 14647346 ACCTTAAGTGATCTGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCACGC ACCTTAAGTGATCTGCCCACCTCGGCCTCCCAGAGTGCTGGGATTACAGGCGTGAGCCACCACGC A G BFAR Ensembl:ENSG00000103429 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1358813007 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_176462,RMVar_hsa_circ_300697,RMVar_hsa_circ_373028,RMVar_hsa_circ_377710,RMVar_hsa_circ_303805,RMVar_hsa_circ_79532,RMVar_hsa_circ_176464,RMVar_hsa_circ_176463,RMVar_hsa_circ_176460,RMVar_hsa_circ_176461 17562 RMVar_ID_17562 Human_SNP_ID_595606392 A-to-I Human chr16 + 14647570 14647570 14647570 TGGTGTAATGGCGCATGCCCATAATCCCAGCTACTCAGGAGGCTGAGACATGAGAATCACTTGAA TGGTGTAATGGCGCATGCCCATAATCCCAGCTTCTCAGGAGGCTGAGACATGAGAATCACTTGAA A T BFAR Ensembl:ENSG00000103429 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1354420776 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_176462,RMVar_hsa_circ_300697,RMVar_hsa_circ_373028,RMVar_hsa_circ_377710,RMVar_hsa_circ_303805,RMVar_hsa_circ_79532,RMVar_hsa_circ_176464,RMVar_hsa_circ_176463,RMVar_hsa_circ_176460,RMVar_hsa_circ_176461 17563 RMVar_ID_17563 Human_SNP_ID_595606393 A-to-I Human chr16 + 14647574 14647574 14647574 GTAATGGCGCATGCCCATAATCCCAGCTACTCAGGAGGCTGAGACATGAGAATCACTTGAAGGAC GTAATGGCGCATGCCCATAATCCCAGCTACTCGGGAGGCTGAGACATGAGAATCACTTGAAGGAC A G BFAR Ensembl:ENSG00000103429 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs556825358 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_176462,RMVar_hsa_circ_300697,RMVar_hsa_circ_373028,RMVar_hsa_circ_377710,RMVar_hsa_circ_303805,RMVar_hsa_circ_79532,RMVar_hsa_circ_176464,RMVar_hsa_circ_176463,RMVar_hsa_circ_176460,RMVar_hsa_circ_176461 17564 RMVar_ID_17564 Human_SNP_ID_595607201 A-to-I Human chr16 + 14650195 14650195 14650195 AATACAAAAAAAAAAAATTGGCCAGGCTTGGTAGTGCACACCTTGTAATCCCATCTATTCGGGAG AATACAAAAAAAAAAAATTGGCCAGGCTTGGTGGTGCACACCTTGTAATCCCATCTATTCGGGAG A G BFAR Ensembl:ENSG00000103429 Protein coding exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs927535375 Functional Loss SNV dbSNP153 33..33 33 - - - 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_111467,RMVar_hsa_circ_176467 17565 RMVar_ID_17565 Human_SNP_ID_595607204 A-to-I Human chr16 + 14650209 14650209 14650209 AAATTGGCCAGGCTTGGTAGTGCACACCTTGTAATCCCATCTATTCGGGAGGCTGAGACAGGAGA AAATTGGCCAGGCTTGGTAGTGCACACCTTGTGATCCCATCTATTCGGGAGGCTGAGACAGGAGA A G BFAR Ensembl:ENSG00000103429 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1184582632 Functional Loss SNV dbSNP153 33..33 33 - - - 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_111467,RMVar_hsa_circ_176467 17566 RMVar_ID_17566 Human_SNP_ID_595607229 A-to-I Human chr16 + 14650305 14650305 14650305 TGAGCCAAGATCATGCCACTGCACTCCAGCCTAGGCAACAAGGCAAGACTCCATCTCAAAAAGAG TGAGCCAAGATCATGCCACTGCACTCCAGCCTTGGCAACAAGGCAAGACTCCATCTCAAAAAGAG A T BFAR Ensembl:ENSG00000103429 Protein coding exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1390772153 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1264874 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_111467,RMVar_hsa_circ_176467 17567 RMVar_ID_17567 Human_SNP_ID_595608783 A-to-I Human chr16 + 14655606 14655606 14655606 CAGGCACACGCCACCACACCAGGCTAATGTTTATGTTTCTAGTAGAGATGGTTTCAGGATGTTGG CAGGCACACGCCACCACACCAGGCTAATGTTTGTGTTTCTAGTAGAGATGGTTTCAGGATGTTGG A G BFAR Ensembl:ENSG00000103429 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1390811955 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_373028,RMVar_hsa_circ_79532,RMVar_hsa_circ_176460,RMVar_hsa_circ_176461,RMVar_hsa_circ_267338,RMVar_hsa_circ_176470,RMVar_hsa_circ_372841,RMVar_hsa_circ_331449,RMVar_hsa_circ_176469 17568 RMVar_ID_17568 Human_SNP_ID_595608951 A-to-I Human chr16 + 14656269 14656267 14656269 ACGCTGTGGGCTGGGCATGGTGGTTCACAACTATAATGCTAGTACTTTGGAAGGCTGAGGTGGGA ACGCTGTGGGCTGGGCATGGTGGTTCACAAC__TAATGCTAGTACTTTGGAAGGCTGAGGTGGGA CTA C BFAR Ensembl:ENSG00000103429 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs368728681 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_6494866 RMVar_hsa_circ_373028,RMVar_hsa_circ_79532,RMVar_hsa_circ_176460,RMVar_hsa_circ_176461,RMVar_hsa_circ_267338,RMVar_hsa_circ_176470,RMVar_hsa_circ_372841,RMVar_hsa_circ_331449,RMVar_hsa_circ_176469 17569 RMVar_ID_17569 Human_SNP_ID_595608953 A-to-I Human chr16 + 14656269 14656269 14656269 ACGCTGTGGGCTGGGCATGGTGGTTCACAACTATAATGCTAGTACTTTGGAAGGCTGAGGTGGGA ACGCTGTGGGCTGGGCATGGTGGTTCACAACTGTAATGCTAGTACTTTGGAAGGCTGAGGTGGGA A G BFAR Ensembl:ENSG00000103429 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs889758297 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6494866 RMVar_hsa_circ_373028,RMVar_hsa_circ_79532,RMVar_hsa_circ_176460,RMVar_hsa_circ_176461,RMVar_hsa_circ_267338,RMVar_hsa_circ_176470,RMVar_hsa_circ_372841,RMVar_hsa_circ_331449,RMVar_hsa_circ_176469 17570 RMVar_ID_17570 Human_SNP_ID_595609351 A-to-I Human chr16 + 14657620 14657620 14657620 ACTGGAGTGCAGTGGTGCGACCTTAGCTCACTACAACCTCTGCCTTCCAGGTTCAAGCAATTCTC ACTGGAGTGCAGTGGTGCGACCTTAGCTCACTGCAACCTCTGCCTTCCAGGTTCAAGCAATTCTC A G BFAR Ensembl:ENSG00000103429 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1293572907 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_373028,RMVar_hsa_circ_79532,RMVar_hsa_circ_176460,RMVar_hsa_circ_176461,RMVar_hsa_circ_267338,RMVar_hsa_circ_176470,RMVar_hsa_circ_372841,RMVar_hsa_circ_331449,RMVar_hsa_circ_176469 17571 RMVar_ID_17571 Human_SNP_ID_595611218 A-to-I Human chr16 + 14663984 14663984 14663984 TTAATTACGGCCGGGTGCGGTGGTTCACTCCTATAATCCAAGCACTTTGGGAGGCAGAGGCGGGC TTAATTACGGCCGGGTGCGGTGGTTCACTCCTGTAATCCAAGCACTTTGGGAGGCAGAGGCGGGC A G BFAR Ensembl:ENSG00000103429 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs975578727 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79532,RMVar_hsa_circ_176460,RMVar_hsa_circ_176470,RMVar_hsa_circ_331449,RMVar_hsa_circ_176471,RMVar_hsa_circ_23371 17572 RMVar_ID_17572 Human_SNP_ID_595613249 A-to-I Human chr16 + 14671344 14671344 14671344 GTAATCATAGCTCACTGCAACTTTGAACTCCTAGGCACAAGTTATCTTCCCTCTTCGGCCTCCCG GTAATCATAGCTCACTGCAACTTTGAACTCCTGGGCACAAGTTATCTTCCCTCTTCGGCCTCCCG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1481641138 Functional Loss SNV dbSNP153 33..33 33 - - - 17573 RMVar_ID_17573 Human_SNP_ID_595662470 A-to-I Human chr16 + 14941314 14941314 14941314 AAAATTAGTCGGGCATGGTGGCAGAGACCTGTAATCTCAGCTGCTCGGGAGGCTGAGGCAGGAGA AAAATTAGTCGGGCATGGTGGCAGAGACCTGTGATCTCAGCTGCTCGGGAGGCTGAGGCAGGAGA A G NPIPA1 Ensembl:ENSG00000183426 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1355129085 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_85249,RMVar_hsa_circ_176488,RMVar_hsa_circ_176495 17574 RMVar_ID_17574 Human_SNP_ID_595674334 A-to-I Human chr16 + 14978856 14978856 14978856 CTTGAGCAAACTTAAAGCAGTTTCTCAGCGTCAGCACTAGTGATATTTTGGGTCAGATAATTTGC CTTGAGCAAACTTAAAGCAGTTTCTCAGCGTCGGCACTAGTGATATTTTGGGTCAGATAATTTGC A G PDXDC1 Ensembl:ENSG00000179889 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs964726282 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12671824 Human_miRNA_ID_2775312,Human_miRNA_ID_2775313,Human_miRNA_ID_2949518,Human_miRNA_ID_2949519 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 17575 RMVar_ID_17575 Human_SNP_ID_595674336 A-to-I Human chr16 + 14978862 14978862 14978862 CAAACTTAAAGCAGTTTCTCAGCGTCAGCACTAGTGATATTTTGGGTCAGATAATTTGCTGTTAT CAAACTTAAAGCAGTTTCTCAGCGTCAGCACTTGTGATATTTTGGGTCAGATAATTTGCTGTTAT A T PDXDC1 Ensembl:ENSG00000179889 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1423410118 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12671824 Human_miRNA_ID_2775312,Human_miRNA_ID_2775313 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 17576 RMVar_ID_17576 Human_SNP_ID_595675632 A-to-I Human chr16 + 14983317 14983317 14983317 TCTCTTGGCCGGGTATGGTGGCTCATGCCTGTAATCTCATCACTTTGGGAGGCCGAGGCGGGCAG TCTCTTGGCCGGGTATGGTGGCTCATGCCTGTCATCTCATCACTTTGGGAGGCCGAGGCGGGCAG A C PDXDC1 Ensembl:ENSG00000179889 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs375216749 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_176497,RMVar_hsa_circ_104826,RMVar_hsa_circ_125777,RMVar_hsa_circ_176498 17577 RMVar_ID_17577 Human_SNP_ID_595675633 A-to-I Human chr16 + 14983317 14983317 14983317 TCTCTTGGCCGGGTATGGTGGCTCATGCCTGTAATCTCATCACTTTGGGAGGCCGAGGCGGGCAG TCTCTTGGCCGGGTATGGTGGCTCATGCCTGTGATCTCATCACTTTGGGAGGCCGAGGCGGGCAG A G PDXDC1 Ensembl:ENSG00000179889 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs375216749 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_176497,RMVar_hsa_circ_104826,RMVar_hsa_circ_125777,RMVar_hsa_circ_176498 17578 RMVar_ID_17578 Human_SNP_ID_595676680 A-to-I Human chr16 + 14985920 14985920 14985920 CAGGAGTTTGAGATCAGCCTGGGTGACATAGTAGGACCATGTCTCTCCAAAAAATTTTTAAAAAT CAGGAGTTTGAGATCAGCCTGGGTGACATAGTGGGACCATGTCTCTCCAAAAAATTTTTAAAAAT A G PDXDC1 Ensembl:ENSG00000179889 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1312080946 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_176497,RMVar_hsa_circ_104826,RMVar_hsa_circ_125777,RMVar_hsa_circ_176498 17579 RMVar_ID_17579 Human_SNP_ID_595678393 A-to-I Human chr16 - 14990968 14990968 14990968 GGAGGCCGAGGTTGACGGATCACCTGAGGCCCAGGAGTTCGAGACCAGCTTGGCTAACACGGCAA GGAGGCCGAGGTTGACGGATCACCTGAGGCCCGGGAGTTCGAGACCAGCTTGGCTAACACGGCAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1477590641 Functional Loss SNV dbSNP153 33..33 33 - - - 17580 RMVar_ID_17580 Human_SNP_ID_595680922 A-to-I Human chr16 + 14999024 14999024 14999024 AGAGGATCACTTGAGCCCAGGAGTTCAAGGTTACAGCGATCTGTGATTGTACCACTGCACTCCAG AGAGGATCACTTGAGCCCAGGAGTTCAAGGTTGCAGCGATCTGTGATTGTACCACTGCACTCCAG A G PDXDC1 Ensembl:ENSG00000179889 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1419417511 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_125777,RMVar_hsa_circ_176498,RMVar_hsa_circ_29630,RMVar_hsa_circ_346735,RMVar_hsa_circ_176500 17581 RMVar_ID_17581 Human_SNP_ID_595681062 A-to-I Human chr16 + 14999447 14999447 14999447 AGTGATACATGGAGCTAGGCACCGTGGTGCACACTTGTAGTCCCAGCTGCTTGGGAGCCTGAGGC AGTGATACATGGAGCTAGGCACCGTGGTGCACCCTTGTAGTCCCAGCTGCTTGGGAGCCTGAGGC A C PDXDC1 Ensembl:ENSG00000179889 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1179949300 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_125777,RMVar_hsa_circ_176498,RMVar_hsa_circ_29630,RMVar_hsa_circ_346735,RMVar_hsa_circ_176500 17582 RMVar_ID_17582 Human_SNP_ID_595681063 A-to-I Human chr16 + 14999447 14999447 14999447 AGTGATACATGGAGCTAGGCACCGTGGTGCACACTTGTAGTCCCAGCTGCTTGGGAGCCTGAGGC AGTGATACATGGAGCTAGGCACCGTGGTGCACGCTTGTAGTCCCAGCTGCTTGGGAGCCTGAGGC A G PDXDC1 Ensembl:ENSG00000179889 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1179949300 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_125777,RMVar_hsa_circ_176498,RMVar_hsa_circ_29630,RMVar_hsa_circ_346735,RMVar_hsa_circ_176500 17583 RMVar_ID_17583 Human_SNP_ID_560921750 A-to-I Human chr14 - 75038986 75038986 75038986 GGGCGTGGTGGCGGGCACCTGTACTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCATGGA GGGCGTGGTGGCGGGCACCTGTACTCCCAGCTGCTCGGGAGGCTGAGGCAGGAGAATGGCATGGA T C MLH3 Ensembl:ENSG00000119684 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs898805107 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96209,RMVar_hsa_circ_167961,RMVar_hsa_circ_167963,RMVar_hsa_circ_104442,RMVar_hsa_circ_376129,RMVar_hsa_circ_167971,RMVar_hsa_circ_44498,RMVar_hsa_circ_167964,RMVar_hsa_circ_167965,RMVar_hsa_circ_47465,RMVar_hsa_circ_270011,RMVar_hsa_circ_356918,RMVar_hsa_circ_167967,RMVar_hsa_circ_107653,RMVar_hsa_circ_325325,RMVar_hsa_circ_329467,RMVar_hsa_circ_167968,RMVar_hsa_circ_167973,RMVar_hsa_circ_326884,RMVar_hsa_circ_167970,RMVar_hsa_circ_348536,RMVar_hsa_circ_323890,RMVar_hsa_circ_167972 17584 RMVar_ID_17584 Human_SNP_ID_560926417 A-to-I Human chr14 - 75057739 75057739 75057739 TGATCTCGAACTCCTGACCTCATGATCCCCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGT TGATCTCGAACTCCTGACCTCATGATCCCCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGT T C ACYP1 Ensembl:ENSG00000119640 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1206426015 Functional Loss SNV dbSNP153 33..33 33 - - - 17585 RMVar_ID_17585 Human_SNP_ID_560926426 A-to-I Human chr14 - 75057762 75057762 75057762 GCGTTTCACCGTCTTGGCCAGGCTGATCTCGAACTCCTGACCTCATGATCCCCCCACCTCGGCCT GCGTTTCACCGTCTTGGCCAGGCTGATCTCGAGCTCCTGACCTCATGATCCCCCCACCTCGGCCT T C ACYP1 Ensembl:ENSG00000119640 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1191650239 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12423645 17586 RMVar_ID_17586 Human_SNP_ID_560933001 A-to-I Human chr14 - 75085131 75085131 75085131 ATGATGGCACACGCCTATAGTCCCAGTTATTCAGGAGGCTGAGGTGGGAAGATCACCTGAATCTG ATGATGGCACACGCCTATAGTCCCAGTTATTCGGGAGGCTGAGGTGGGAAGATCACCTGAATCTG T C NEK9 Ensembl:ENSG00000119638 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985142611 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87237,RMVar_hsa_circ_167980 17587 RMVar_ID_17587 Human_SNP_ID_560940288 A-to-I Human chr14 - 75115389 75115389 75115389 TCAGAGGCTGGGCGCGGTGGCTCATGCCTGTGATCCCAGCACTTTGGGAGGCTGAGGCGGACAGA TCAGAGGCTGGGCGCGGTGGCTCATGCCTGTGTTCCCAGCACTTTGGGAGGCTGAGGCGGACAGA T A NEK9 Ensembl:ENSG00000119638 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs958130983 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1720,RMVar_hsa_circ_337374,RMVar_hsa_circ_373485,RMVar_hsa_circ_106406,RMVar_hsa_circ_167988,RMVar_hsa_circ_7183,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_81826,RMVar_hsa_circ_37035,RMVar_hsa_circ_168002,RMVar_hsa_circ_353739,RMVar_hsa_circ_373442,RMVar_hsa_circ_50221,RMVar_hsa_circ_168006,RMVar_hsa_circ_291746,RMVar_hsa_circ_344495,RMVar_hsa_circ_309676,RMVar_hsa_circ_357383,RMVar_hsa_circ_309996,RMVar_hsa_circ_281858,RMVar_hsa_circ_168007,RMVar_hsa_circ_168009,RMVar_hsa_circ_168010,RMVar_hsa_circ_168008,RMVar_hsa_circ_117853,RMVar_hsa_circ_168013,RMVar_hsa_circ_334276,RMVar_hsa_circ_110258,RMVar_hsa_circ_291648,RMVar_hsa_circ_168014,RMVar_hsa_circ_168016,RMVar_hsa_circ_101734,RMVar_hsa_circ_168015 17588 RMVar_ID_17588 Human_SNP_ID_560940465 A-to-I Human chr14 - 75116201 75116201 75116201 CCTCAAGTGATCCTCCTGCCTTGGCCTGTGCTAGGATTACAGGTATGAGCCCCCATGCCCAGCAT CCTCAAGTGATCCTCCTGCCTTGGCCTGTGCTGGGATTACAGGTATGAGCCCCCATGCCCAGCAT T C NEK9 Ensembl:ENSG00000119638 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202589589 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1720,RMVar_hsa_circ_337374,RMVar_hsa_circ_373485,RMVar_hsa_circ_106406,RMVar_hsa_circ_167988,RMVar_hsa_circ_7183,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_81826,RMVar_hsa_circ_37035,RMVar_hsa_circ_168002,RMVar_hsa_circ_353739,RMVar_hsa_circ_373442,RMVar_hsa_circ_50221,RMVar_hsa_circ_168006,RMVar_hsa_circ_291746,RMVar_hsa_circ_344495,RMVar_hsa_circ_309676,RMVar_hsa_circ_357383,RMVar_hsa_circ_309996,RMVar_hsa_circ_281858,RMVar_hsa_circ_168007,RMVar_hsa_circ_168009,RMVar_hsa_circ_168010,RMVar_hsa_circ_168008,RMVar_hsa_circ_117853,RMVar_hsa_circ_168013,RMVar_hsa_circ_334276,RMVar_hsa_circ_110258,RMVar_hsa_circ_291648,RMVar_hsa_circ_168014,RMVar_hsa_circ_168016,RMVar_hsa_circ_101734,RMVar_hsa_circ_168017,RMVar_hsa_circ_168015 17589 RMVar_ID_17589 Human_SNP_ID_560940570 A-to-I Human chr14 - 75116701 75116701 75116701 ATCACTTGAACCCGGGAAGTGGAGACTGCAGTAAGCCAAGATCGCACCACTGTACTCCAGCCTGG ATCACTTGAACCCGGGAAGTGGAGACTGCAGTGAGCCAAGATCGCACCACTGTACTCCAGCCTGG T C NEK9 Ensembl:ENSG00000119638 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1173997766 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1720,RMVar_hsa_circ_337374,RMVar_hsa_circ_373485,RMVar_hsa_circ_106406,RMVar_hsa_circ_167988,RMVar_hsa_circ_7183,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_81826,RMVar_hsa_circ_37035,RMVar_hsa_circ_168002,RMVar_hsa_circ_353739,RMVar_hsa_circ_373442,RMVar_hsa_circ_50221,RMVar_hsa_circ_168006,RMVar_hsa_circ_291746,RMVar_hsa_circ_344495,RMVar_hsa_circ_309676,RMVar_hsa_circ_357383,RMVar_hsa_circ_309996,RMVar_hsa_circ_281858,RMVar_hsa_circ_168007,RMVar_hsa_circ_168009,RMVar_hsa_circ_168010,RMVar_hsa_circ_168008,RMVar_hsa_circ_117853,RMVar_hsa_circ_168013,RMVar_hsa_circ_334276,RMVar_hsa_circ_110258,RMVar_hsa_circ_291648,RMVar_hsa_circ_168014,RMVar_hsa_circ_168016,RMVar_hsa_circ_101734,RMVar_hsa_circ_168017,RMVar_hsa_circ_168015 17590 RMVar_ID_17590 Human_SNP_ID_560941998 A-to-I Human chr14 - 75123003 75123003 75123003 ATCACTTGAGCATAGGAGTTTGAGGAAAGCCTAGGCAACATAGTGAAACCCTGTCACTACCAAAA ATCACTTGAGCATAGGAGTTTGAGGAAAGCCTGGGCAACATAGTGAAACCCTGTCACTACCAAAA T C NEK9 Ensembl:ENSG00000119638 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1228042066 Functional Loss SNV dbSNP153 33..33 33 - - - 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 17591 RMVar_ID_17591 Human_SNP_ID_560944478 A-to-I Human chr14 - 75132420 75132420 75132420 CCAAGTAGAGAAAATAATATGTGGGTTAAGATACATCCTTAAACTTTTTTTTTTTTGGGGGGGGG CCAAGTAGAGAAAATAATATGTGGGTTAAGATTCATCCTTAAACTTTTTTTTTTTTGGGGGGGGG T A TMED10 Ensembl:ENSG00000170348 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1429217558 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_452002,Human_RBP_ID_6385723,Human_RBP_ID_17480307,Human_RBP_ID_17853586,Human_RBP_ID_18276213,Human_RBP_ID_27647746 17592 RMVar_ID_17592 Human_SNP_ID_560945573 A-to-I Human chr14 + 75137411 75137411 75137411 AATTCTGTTTCTGGCCGGGTGTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGT AATTCTGTTTCTGGCCGGGTGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1476289020 Functional Loss SNV dbSNP153 33..33 33 - - - 17593 RMVar_ID_17593 Human_SNP_ID_560949683 A-to-I Human chr14 - 75155097 75155097 75155097 AAAATTAGCCGGGCTTGGGGGTGCATGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA AAAATTAGCCGGGCTTGGGGGTGCATGCCTGTGGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA T C TMED10 Ensembl:ENSG00000170348 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs774811708 Functional Loss SNV dbSNP153 33..33 33 - - - 17594 RMVar_ID_17594 Human_SNP_ID_560951481 A-to-I Human chr14 - 75163431 75163431 75163431 CTGCTGCCTCAGCTGCCTGAGTAGCTGGGACTACAGGCGAGTGCCACCATGCCCGGCTAGTTTTT CTGCTGCCTCAGCTGCCTGAGTAGCTGGGACTGCAGGCGAGTGCCACCATGCCCGGCTAGTTTTT T C TMED10 Ensembl:ENSG00000170348 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs575460701 Functional Loss SNV dbSNP153 33..33 33 - - - 17595 RMVar_ID_17595 Human_SNP_ID_560954025 A-to-I Human chr14 - 75173203 75173203 75173203 TTCATATTTGTTTGTAGAAATGGAGTTTCGCCATGTTACCCAGGCTGGTCTCGAACTCCTGGGCT TTCATATTTGTTTGTAGAAATGGAGTTTCGCCGTGTTACCCAGGCTGGTCTCGAACTCCTGGGCT T C TMED10 Ensembl:ENSG00000170348 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs530346811 Functional Loss SNV dbSNP153 33..33 33 - - - 17596 RMVar_ID_17596 Human_SNP_ID_560954026 A-to-I Human chr14 - 75173203 75173203 75173203 TTCATATTTGTTTGTAGAAATGGAGTTTCGCCATGTTACCCAGGCTGGTCTCGAACTCCTGGGCT TTCATATTTGTTTGTAGAAATGGAGTTTCGCCCTGTTACCCAGGCTGGTCTCGAACTCCTGGGCT T G TMED10 Ensembl:ENSG00000170348 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs530346811 Functional Loss SNV dbSNP153 33..33 33 - - - 17597 RMVar_ID_17597 Human_SNP_ID_561054422 A-to-I Human chr14 + 75588562 75588562 75588562 TGGAGTTCACAGACAGCATCTTGGCTCACTGCAATCTCCACTTCCCGATTCAAGCAATTCTGCCT TGGAGTTCACAGACAGCATCTTGGCTCACTGCCATCTCCACTTCCCGATTCAAGCAATTCTGCCT A C FLVCR2 Ensembl:ENSG00000119686 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1171857622 Functional Loss SNV dbSNP153 33..33 33 - - - 17598 RMVar_ID_17598 Human_SNP_ID_561056076 A-to-I Human chr14 + 75595888 75595888 75595888 GACTTTCCTCATTCTGTTCTTGCGTTCCTCTCATTGCTTTCTTGAGGTCTTTTTCTTCTCATACA GACTTTCCTCATTCTGTTCTTGCGTTCCTCTCGTTGCTTTCTTGAGGTCTTTTTCTTCTCATACA A G FLVCR2 Ensembl:ENSG00000119686 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs879043070 Functional Loss SNV dbSNP153 33..33 33 - - - 17599 RMVar_ID_17599 Human_SNP_ID_561069086 A-to-I Human chr14 - 75653453 75653453 75653453 GGATTACAGGCGCGCACCACCATGCCCCTCTAATTTTTGTATTTTTAGTAGAGACAGGTTCTCAC GGATTACAGGCGCGCACCACCATGCCCCTCTATTTTTTGTATTTTTAGTAGAGACAGGTTCTCAC T A ERG28 Ensembl:ENSG00000133935 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs999562494 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85150,RMVar_hsa_circ_168038 17600 RMVar_ID_17600 Human_SNP_ID_561069096 A-to-I Human chr14 - 75653493 75653493 75653493 GGTTTAAGCCATTCTCCTGCCTCAGCCTCCCCAGTAGCTGGGATTACAGGCGCGCACCACCATGC GGTTTAAGCCATTCTCCTGCCTCAGCCTCCCCCGTAGCTGGGATTACAGGCGCGCACCACCATGC T G ERG28 Ensembl:ENSG00000133935 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1321990141 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85150,RMVar_hsa_circ_168038 17601 RMVar_ID_17601 Human_SNP_ID_561101305 A-to-I Human chr14 + 75790717 75790717 75790717 GAACTTCTGTGCTAAAGTGGCCCTCCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG GAACTTCTGTGCTAAAGTGGCCCTCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG A G TTLL5 Ensembl:ENSG00000119685 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs373657307 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_50529,RMVar_hsa_circ_1492,RMVar_hsa_circ_59400,RMVar_hsa_circ_168065,RMVar_hsa_circ_85137,RMVar_hsa_circ_81757,RMVar_hsa_circ_168064,RMVar_hsa_circ_365276,RMVar_hsa_circ_311873,RMVar_hsa_circ_325643,RMVar_hsa_circ_288684,RMVar_hsa_circ_31393,RMVar_hsa_circ_11154,RMVar_hsa_circ_43235,RMVar_hsa_circ_23027,RMVar_hsa_circ_43191,RMVar_hsa_circ_355651,RMVar_hsa_circ_315666,RMVar_hsa_circ_311770,RMVar_hsa_circ_75973,RMVar_hsa_circ_168075,RMVar_hsa_circ_168076,RMVar_hsa_circ_168077,RMVar_hsa_circ_364500,RMVar_hsa_circ_23983,RMVar_hsa_circ_168078,RMVar_hsa_circ_168084,RMVar_hsa_circ_354609,RMVar_hsa_circ_168083,RMVar_hsa_circ_117453,RMVar_hsa_circ_168085 17602 RMVar_ID_17602 Human_SNP_ID_561171048 A-to-I Human chr14 - 76082608 76082608 76082608 GTCATCACCCGCTTTATCTGGATGCTGAAGGAAAGAGAGAGCGAGAGGCGGGAACCCCAGGCAGG GTCATCACCCGCTTTATCTGGATGCTGAAGGAGAGAGAGAGCGAGAGGCGGGAACCCCAGGCAGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs774571610 Functional Loss SNV dbSNP153 33..33 33 - - - 17603 RMVar_ID_17603 Human_SNP_ID_561200055 A-to-I Human chr14 + 76205063 76205060 76205064 GTGTTCATAGCTCACTGTAACCTTGAACTCATAAGCTCAAGCCATCCTCCTGCCTCAGCCTCCTG GTGTTCATAGCTCACTGTAACCTTGAACTC____GCTCAAGCCATCCTCCTGCCTCAGCCTCCTG CATAA C GPATCH2L Ensembl:ENSG00000089916 Protein coding 3'UTR GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1333994849 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_22925359 17604 RMVar_ID_17604 Human_SNP_ID_561370431 A-to-I Human chr14 - 76886661 76886661 76886661 AAGTTCACTCTTGATTGCACCCACCCTGTAGAAGATGGAATCATGGATGCTGCCAATTTTGAGCA AAGTTCACTCTTGATTGCACCCACCCTGTAGAGGATGGAATCATGGATGCTGCCAATTTTGAGCA T C RPL22P2 Ensembl:ENSG00000241081 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs998209906 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4309340,Human_RBP_ID_5095659,Human_RBP_ID_17363915 Human_miRNA_ID_1817518,Human_miRNA_ID_1818280 17605 RMVar_ID_17605 Human_SNP_ID_561392208 A-to-I Human chr14 + 76970547 76970547 76970547 TATATTTTTTATTAGTGAAGAGGTTTCGCCATATTGGCCAGACTGGTCTCGAACTCCTGACCTCA TATATTTTTTATTAGTGAAGAGGTTTCGCCATGTTGGCCAGACTGGTCTCGAACTCCTGACCTCA A G LINC01629,LINC01629:2,LINC01629:3,LINC01629:4 RNACentral:URS0000D5BCC5,RNACentral:URS0000D58C96,RNACentral:URS0000D5ABC1,RNACentral:URS0000D5DD82 lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1312409265 Functional Loss SNV dbSNP153 33..33 33 - - - 17606 RMVar_ID_17606 Human_SNP_ID_561428434 A-to-I Human chr14 + 77108623 77108623 77108623 TGAGGCAGGAGAACCGCTTGAACCCGGGAGGCAGAGGTTGTGGTGAGCTAAGATCATGCCATTGC TGAGGCAGGAGAACCGCTTGAACCCGGGAGGCGGAGGTTGTGGTGAGCTAAGATCATGCCATTGC A G AC007375.2,CIPC Ensembl:ENSG00000259164,Ensembl:ENSG00000198894 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1012414643 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_359349 17607 RMVar_ID_17607 Human_SNP_ID_561475841 A-to-I Human chr14 - 77294446 77294446 77294446 TTGATGGCACGTGCCAGTAATCCCAGCCACTCAGGAGACTGAGGCAGGAGAATCACTTGAACCGG TTGATGGCACGTGCCAGTAATCCCAGCCACTCGGGAGACTGAGGCAGGAGAATCACTTGAACCGG T C POMT2 Ensembl:ENSG00000009830 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017240767 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24136,RMVar_hsa_circ_109755,RMVar_hsa_circ_168147,RMVar_hsa_circ_110984,RMVar_hsa_circ_168150,RMVar_hsa_circ_102815,RMVar_hsa_circ_168152 17608 RMVar_ID_17608 Human_SNP_ID_561475844 A-to-I Human chr14 - 77294450 77294450 77294450 GGGCTTGATGGCACGTGCCAGTAATCCCAGCCACTCAGGAGACTGAGGCAGGAGAATCACTTGAA GGGCTTGATGGCACGTGCCAGTAATCCCAGCCTCTCAGGAGACTGAGGCAGGAGAATCACTTGAA T A POMT2 Ensembl:ENSG00000009830 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs780031019 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24136,RMVar_hsa_circ_109755,RMVar_hsa_circ_168147,RMVar_hsa_circ_110984,RMVar_hsa_circ_168150,RMVar_hsa_circ_102815,RMVar_hsa_circ_168152 17609 RMVar_ID_17609 Human_SNP_ID_561475845 A-to-I Human chr14 - 77294450 77294450 77294450 GGGCTTGATGGCACGTGCCAGTAATCCCAGCCACTCAGGAGACTGAGGCAGGAGAATCACTTGAA GGGCTTGATGGCACGTGCCAGTAATCCCAGCCGCTCAGGAGACTGAGGCAGGAGAATCACTTGAA T C POMT2 Ensembl:ENSG00000009830 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs780031019 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24136,RMVar_hsa_circ_109755,RMVar_hsa_circ_168147,RMVar_hsa_circ_110984,RMVar_hsa_circ_168150,RMVar_hsa_circ_102815,RMVar_hsa_circ_168152 17610 RMVar_ID_17610 Human_SNP_ID_561475850 A-to-I Human chr14 - 77294463 77294463 77294463 AAAAAAATTACTCGGGCTTGATGGCACGTGCCAGTAATCCCAGCCACTCAGGAGACTGAGGCAGG AAAAAAATTACTCGGGCTTGATGGCACGTGCCTGTAATCCCAGCCACTCAGGAGACTGAGGCAGG T A POMT2 Ensembl:ENSG00000009830 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1023874860 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24136,RMVar_hsa_circ_109755,RMVar_hsa_circ_168147,RMVar_hsa_circ_110984,RMVar_hsa_circ_168150,RMVar_hsa_circ_102815,RMVar_hsa_circ_168152 17611 RMVar_ID_17611 Human_SNP_ID_561475851 A-to-I Human chr14 - 77294463 77294463 77294463 AAAAAAATTACTCGGGCTTGATGGCACGTGCCAGTAATCCCAGCCACTCAGGAGACTGAGGCAGG AAAAAAATTACTCGGGCTTGATGGCACGTGCCGGTAATCCCAGCCACTCAGGAGACTGAGGCAGG T C POMT2 Ensembl:ENSG00000009830 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1023874860 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24136,RMVar_hsa_circ_109755,RMVar_hsa_circ_168147,RMVar_hsa_circ_110984,RMVar_hsa_circ_168150,RMVar_hsa_circ_102815,RMVar_hsa_circ_168152 17612 RMVar_ID_17612 Human_SNP_ID_561480251 A-to-I Human chr14 - 77312505 77312505 77312505 GCACGTGCCACCATGCCTGGCTAATTTTTTGTATTTTTAGTAGAGACAGGGTTTTACCATGTTAG GCACGTGCCACCATGCCTGGCTAATTTTTTGTGTTTTTAGTAGAGACAGGGTTTTACCATGTTAG T C POMT2 Ensembl:ENSG00000009830 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs934705434 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112122,RMVar_hsa_circ_168157 17613 RMVar_ID_17613 Human_SNP_ID_561483422 A-to-I Human chr14 + 77324236 77324236 77324236 GCGATCTCGGCCCACTGTGACCTCCACCTCTCAGGTTCAAGCTATTCTCTTACCTCAACCTCCTG GCGATCTCGGCCCACTGTGACCTCCACCTCTCGGGTTCAAGCTATTCTCTTACCTCAACCTCCTG A G GSTZ1 Ensembl:ENSG00000100577 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1412164129 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93609,RMVar_hsa_circ_168159 17614 RMVar_ID_17614 Human_SNP_ID_561499743 A-to-I Human chr14 + 77391501 77391501 77391501 CATCATGCCCAGCTAATTTTTGTATTTTTAGTAGATATGATGTTTCACCATGTTGGCCAGGCTGG CATCATGCCCAGCTAATTTTTGTATTTTTAGTGGATATGATGTTTCACCATGTTGGCCAGGCTGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1286587561 Functional Loss SNV dbSNP153 33..33 33 - - - 17615 RMVar_ID_17615 Human_SNP_ID_561501113 A-to-I Human chr14 - 77397668 77397668 77397668 TGGCCAGCCTGGTCTTGAACTCCTGACCTCAAATGATCCGCCTGCCTTGGCCTCCCAAAGTGCTG TGGCCAGCCTGGTCTTGAACTCCTGACCTCAAGTGATCCGCCTGCCTTGGCCTCCCAAAGTGCTG T C NOXRED1 Ensembl:ENSG00000165555 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1245516609 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_168165 17616 RMVar_ID_17616 Human_SNP_ID_561516590 A-to-I Human chr14 + 77461479 77461479 77461479 TTGAACCTGGGAGGTGGAGGTTGCAATGAGCCAAGATCATGCCACTGCAATCCAGCCTGAGCGAC TTGAACCTGGGAGGTGGAGGTTGCAATGAGCCGAGATCATGCCACTGCAATCCAGCCTGAGCGAC A G AHSA1 Ensembl:ENSG00000100591 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1286932798 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125141,RMVar_hsa_circ_67229,RMVar_hsa_circ_168182 17617 RMVar_ID_17617 Human_SNP_ID_561517836 A-to-I Human chr14 + 77465999 77465999 77465999 TAGGCACACGCCATCACGCCTAGCTAATTTTTATGTTTTTTAGTAGAGATGGGGTTTCACCATAT TAGGCACACGCCATCACGCCTAGCTAATTTTTGTGTTTTTTAGTAGAGATGGGGTTTCACCATAT A G AHSA1 Ensembl:ENSG00000100591 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs966892475 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7293,RMVar_hsa_circ_125141,RMVar_hsa_circ_168182,RMVar_hsa_circ_106434,RMVar_hsa_circ_113560,RMVar_hsa_circ_286380,RMVar_hsa_circ_168184,RMVar_hsa_circ_168186,RMVar_hsa_circ_168187,RMVar_hsa_circ_82213,RMVar_hsa_circ_104152,RMVar_hsa_circ_168188,RMVar_hsa_circ_168189 17618 RMVar_ID_17618 Human_SNP_ID_561517892 A-to-I Human chr14 + 77466250 77466250 77466250 CTCCTTCCTCAGCCTCCTGAGTAGCTGGGACTACAGGTGCACACTACCGTGCCTGTTCCAGTTTT CTCCTTCCTCAGCCTCCTGAGTAGCTGGGACTGCAGGTGCACACTACCGTGCCTGTTCCAGTTTT A G AHSA1 Ensembl:ENSG00000100591 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs906951574 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7293,RMVar_hsa_circ_125141,RMVar_hsa_circ_168182,RMVar_hsa_circ_106434,RMVar_hsa_circ_113560,RMVar_hsa_circ_286380,RMVar_hsa_circ_168184,RMVar_hsa_circ_168186,RMVar_hsa_circ_168187,RMVar_hsa_circ_82213,RMVar_hsa_circ_104152,RMVar_hsa_circ_168188,RMVar_hsa_circ_168189 17619 RMVar_ID_17619 Human_SNP_ID_561518106 A-to-I Human chr14 + 77467252 77467252 77467252 GAAGCCCTGTCTCTACAAAAAATACAAAAATTAGCCAGGTATGGTGGTATGCGCCTGTAGTCCCA GAAGCCCTGTCTCTACAAAAAATACAAAAATTGGCCAGGTATGGTGGTATGCGCCTGTAGTCCCA A G AHSA1 Ensembl:ENSG00000100591 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs951408331 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7293,RMVar_hsa_circ_125141,RMVar_hsa_circ_168182,RMVar_hsa_circ_106434,RMVar_hsa_circ_113560,RMVar_hsa_circ_286380,RMVar_hsa_circ_168184,RMVar_hsa_circ_168186,RMVar_hsa_circ_168187,RMVar_hsa_circ_82213,RMVar_hsa_circ_104152,RMVar_hsa_circ_168188,RMVar_hsa_circ_168189 17620 RMVar_ID_17620 Human_SNP_ID_561518125 A-to-I Human chr14 + 77467324 77467324 77467324 AGGAGGCTGAGGTGGGAGGATCACCTAAGCTTAGGAGGTCGGGGCTGCAGTGAGCCATGATCATG AGGAGGCTGAGGTGGGAGGATCACCTAAGCTTCGGAGGTCGGGGCTGCAGTGAGCCATGATCATG A C AHSA1 Ensembl:ENSG00000100591 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1178757916 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7293,RMVar_hsa_circ_125141,RMVar_hsa_circ_168182,RMVar_hsa_circ_106434,RMVar_hsa_circ_113560,RMVar_hsa_circ_286380,RMVar_hsa_circ_168184,RMVar_hsa_circ_168186,RMVar_hsa_circ_168187,RMVar_hsa_circ_82213,RMVar_hsa_circ_104152,RMVar_hsa_circ_168188,RMVar_hsa_circ_168189 17621 RMVar_ID_17621 Human_SNP_ID_561518183 A-to-I Human chr14 + 77467539 77467539 77467539 GATGGTGAAACCCCATCTCTACTAAAAAATACAAAAAGTTAGCCAGGCATGGTGGCATGCGCCTG GATGGTGAAACCCCATCTCTACTAAAAAATACGAAAAGTTAGCCAGGCATGGTGGCATGCGCCTG A G AHSA1 Ensembl:ENSG00000100591 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1025713298 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7293,RMVar_hsa_circ_125141,RMVar_hsa_circ_168182,RMVar_hsa_circ_106434,RMVar_hsa_circ_113560,RMVar_hsa_circ_286380,RMVar_hsa_circ_168184,RMVar_hsa_circ_168186,RMVar_hsa_circ_168187,RMVar_hsa_circ_82213,RMVar_hsa_circ_104152,RMVar_hsa_circ_168188,RMVar_hsa_circ_168189 17622 RMVar_ID_17622 Human_SNP_ID_561518191 A-to-I Human chr14 + 77467563 77467563 77467563 AAAAATACAAAAAGTTAGCCAGGCATGGTGGCATGCGCCTGTAATCCCAGCTACTACAGAGGCTG AAAAATACAAAAAGTTAGCCAGGCATGGTGGCGTGCGCCTGTAATCCCAGCTACTACAGAGGCTG A G AHSA1 Ensembl:ENSG00000100591 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1272502319 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7293,RMVar_hsa_circ_125141,RMVar_hsa_circ_168182,RMVar_hsa_circ_106434,RMVar_hsa_circ_113560,RMVar_hsa_circ_286380,RMVar_hsa_circ_168184,RMVar_hsa_circ_168186,RMVar_hsa_circ_168187,RMVar_hsa_circ_82213,RMVar_hsa_circ_104152,RMVar_hsa_circ_168188,RMVar_hsa_circ_168189 17623 RMVar_ID_17623 Human_SNP_ID_561518198 A-to-I Human chr14 + 77467573 77467573 77467573 AAAGTTAGCCAGGCATGGTGGCATGCGCCTGTAATCCCAGCTACTACAGAGGCTGAAGCAGAGAA AAAGTTAGCCAGGCATGGTGGCATGCGCCTGTGATCCCAGCTACTACAGAGGCTGAAGCAGAGAA A G AHSA1 Ensembl:ENSG00000100591 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1342194847 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8410854 RMVar_hsa_circ_7293,RMVar_hsa_circ_125141,RMVar_hsa_circ_168182,RMVar_hsa_circ_106434,RMVar_hsa_circ_113560,RMVar_hsa_circ_286380,RMVar_hsa_circ_168184,RMVar_hsa_circ_168186,RMVar_hsa_circ_168187,RMVar_hsa_circ_82213,RMVar_hsa_circ_104152,RMVar_hsa_circ_168188,RMVar_hsa_circ_168189 17624 RMVar_ID_17624 Human_SNP_ID_561518217 A-to-I Human chr14 + 77467644 77467644 77467644 AAAACCTGGACGGGCGGAGGTTGCGTGAGCCGAGATCGCGCCACTGCACTCCAGCCTGGGCAACA AAAACCTGGACGGGCGGAGGTTGCGTGAGCCGCGATCGCGCCACTGCACTCCAGCCTGGGCAACA A C AHSA1 Ensembl:ENSG00000100591 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1337000245 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7293,RMVar_hsa_circ_125141,RMVar_hsa_circ_168182,RMVar_hsa_circ_106434,RMVar_hsa_circ_113560,RMVar_hsa_circ_286380,RMVar_hsa_circ_168184,RMVar_hsa_circ_168186,RMVar_hsa_circ_168187,RMVar_hsa_circ_82213,RMVar_hsa_circ_104152,RMVar_hsa_circ_168188,RMVar_hsa_circ_168189 17625 RMVar_ID_17625 Human_SNP_ID_561537249 A-to-I Human chr14 - 77540034 77540034 77540034 GTGTCACCACACCTGGCTCATTTTGTATTTTTAGTAGAGACAGGGTTTCTTCATGTTGGTCAGGC GTGTCACCACACCTGGCTCATTTTGTATTTTTGGTAGAGACAGGGTTTCTTCATGTTGGTCAGGC T C SPTLC2 Ensembl:ENSG00000100596 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893234698 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56993,RMVar_hsa_circ_268113,RMVar_hsa_circ_357035,RMVar_hsa_circ_122712,RMVar_hsa_circ_36498,RMVar_hsa_circ_168196 17626 RMVar_ID_17626 Human_SNP_ID_561542300 A-to-I Human chr14 - 77559775 77559775 77559775 ATGATTCTCCTGCCTCAGTCTCCTGAGTAGCTAGGACTGTAGGCATCCACCACCATGCCGGACTA ATGATTCTCCTGCCTCAGTCTCCTGAGTAGCTGGGACTGTAGGCATCCACCACCATGCCGGACTA T C SPTLC2 Ensembl:ENSG00000100596 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1051184151 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12430581 RMVar_hsa_circ_35699,RMVar_hsa_circ_357035,RMVar_hsa_circ_122712,RMVar_hsa_circ_168196,RMVar_hsa_circ_313502,RMVar_hsa_circ_297163,RMVar_hsa_circ_126944,RMVar_hsa_circ_6529,RMVar_hsa_circ_44168,RMVar_hsa_circ_168198,RMVar_hsa_circ_168199,RMVar_hsa_circ_124199,RMVar_hsa_circ_168201,RMVar_hsa_circ_30185,RMVar_hsa_circ_285138,RMVar_hsa_circ_377087,RMVar_hsa_circ_127178,RMVar_hsa_circ_168203,RMVar_hsa_circ_168204,RMVar_hsa_circ_168202 17627 RMVar_ID_17627 Human_SNP_ID_561542493 A-to-I Human chr14 - 77560571 77560571 77560571 TTGCTCTGTCTCCCAGGCTGGCATGCATTGGCATGAACTCAGCTCACTGCAACCTCTACCTCCCC TTGCTCTGTCTCCCAGGCTGGCATGCATTGGCGTGAACTCAGCTCACTGCAACCTCTACCTCCCC T C SPTLC2 Ensembl:ENSG00000100596 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991644809 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35699,RMVar_hsa_circ_357035,RMVar_hsa_circ_122712,RMVar_hsa_circ_168196,RMVar_hsa_circ_313502,RMVar_hsa_circ_297163,RMVar_hsa_circ_126944,RMVar_hsa_circ_6529,RMVar_hsa_circ_44168,RMVar_hsa_circ_168198,RMVar_hsa_circ_168199,RMVar_hsa_circ_124199,RMVar_hsa_circ_168201,RMVar_hsa_circ_30185,RMVar_hsa_circ_285138,RMVar_hsa_circ_377087,RMVar_hsa_circ_127178,RMVar_hsa_circ_168203,RMVar_hsa_circ_168204,RMVar_hsa_circ_168202 17628 RMVar_ID_17628 Human_SNP_ID_561571952 A-to-I Human chr14 - 77673505 77673505 77673505 TCTCAGCCTCTGCTATTTCCTTTGAGGAAGGTAGAAGTGAGTTTCCATGTTTGCAGAGTATTTAA TCTCAGCCTCTGCTATTTCCTTTGAGGAAGGTGGAAGTGAGTTTCCATGTTTGCAGAGTATTTAA T C ALKBH1 Ensembl:ENSG00000100601 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs921776507 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1824940,Human_RBP_ID_12430747,Human_RBP_ID_23638283 17629 RMVar_ID_17629 Human_SNP_ID_561572321 A-to-I Human chr14 - 77674825 77674825 77674825 TCAATAGGCTGGGCATGATGGCTTACACCTATAATCCCAGTACTTTGGGAGGCCGAGGCCAGTGG TCAATAGGCTGGGCATGATGGCTTACACCTATGATCCCAGTACTTTGGGAGGCCGAGGCCAGTGG T C ALKBH1 Ensembl:ENSG00000100601 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1259066632 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_168210 17630 RMVar_ID_17630 Human_SNP_ID_561572322 A-to-I Human chr14 - 77674831 77674831 77674831 GACACATCAATAGGCTGGGCATGATGGCTTACACCTATAATCCCAGTACTTTGGGAGGCCGAGGC GACACATCAATAGGCTGGGCATGATGGCTTACGCCTATAATCCCAGTACTTTGGGAGGCCGAGGC T C ALKBH1 Ensembl:ENSG00000100601 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1338403183 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_168210 17631 RMVar_ID_17631 Human_SNP_ID_561572431 A-to-I Human chr14 - 77675312 77675312 77675312 CTCCTGCCTTAGCCTCCTGAGTAGCTGGAACTACAGGTGCACACCGCCACACCCAGCTAATTTTT CTCCTGCCTTAGCCTCCTGAGTAGCTGGAACTGCAGGTGCACACCGCCACACCCAGCTAATTTTT T C ALKBH1 Ensembl:ENSG00000100601 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1218865649 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_168210 17632 RMVar_ID_17632 Human_SNP_ID_561575002 A-to-I Human chr14 - 77684775 77684775 77684775 GGGAGGCCAACGCAGAAGGATTGATTGAAGCTAGAAGTTCAAGACCCACCTGGGCAACATAGAGA GGGAGGCCAACGCAGAAGGATTGATTGAAGCTGGAAGTTCAAGACCCACCTGGGCAACATAGAGA T C ALKBH1 Ensembl:ENSG00000100601 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs888370020 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12430842 RMVar_hsa_circ_55487,RMVar_hsa_circ_51638 17633 RMVar_ID_17633 Human_SNP_ID_561579746 A-to-I Human chr14 - 77703030 77703030 77703030 GTGATTCTTCTGCCTCCCGAGTAGCTGAGACTACAGGTATATGCCACCACGCCCAGCTAATTTTT GTGATTCTTCTGCCTCCCGAGTAGCTGAGACTGCAGGTATATGCCACCACGCCCAGCTAATTTTT T C ALKBH1 Ensembl:ENSG00000100601 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs982507962 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55487,RMVar_hsa_circ_358925 17634 RMVar_ID_17634 Human_SNP_ID_561579749 A-to-I Human chr14 - 77703040 77703040 77703040 CCAGGTTCAAGTGATTCTTCTGCCTCCCGAGTAGCTGAGACTACAGGTATATGCCACCACGCCCA CCAGGTTCAAGTGATTCTTCTGCCTCCCGAGTGGCTGAGACTACAGGTATATGCCACCACGCCCA T C ALKBH1 Ensembl:ENSG00000100601 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs374373921 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55487,RMVar_hsa_circ_358925 17635 RMVar_ID_17635 Human_SNP_ID_561583567 A-to-I Human chr14 + 77716389 77716389 77716389 CGGTGGTAGGCCAGGCGCAGTGGTTCATGCCTATAATCCCAGCACTTTGGGAGGCCGAGGCGGGG CGGTGGTAGGCCAGGCGCAGTGGTTCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGG A G SLIRP Ensembl:ENSG00000119705 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1260610337 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103903,RMVar_hsa_circ_88743,RMVar_hsa_circ_168212,RMVar_hsa_circ_168213 17636 RMVar_ID_17636 Human_SNP_ID_561583643 A-to-I Human chr14 + 77716540 77716540 77716540 GGGCGTGGTGGCACATGCCTGTAGTCCCAGCTACTCAGGAGACTGAGGCAGGAGAACCCAAGAGA GGGCGTGGTGGCACATGCCTGTAGTCCCAGCTGCTCAGGAGACTGAGGCAGGAGAACCCAAGAGA A G SLIRP Ensembl:ENSG00000119705 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs944240895 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103903,RMVar_hsa_circ_88743,RMVar_hsa_circ_168212,RMVar_hsa_circ_168213 17637 RMVar_ID_17637 Human_SNP_ID_561583644 A-to-I Human chr14 + 77716540 77716540 77716540 GGGCGTGGTGGCACATGCCTGTAGTCCCAGCTACTCAGGAGACTGAGGCAGGAGAACCCAAGAGA GGGCGTGGTGGCACATGCCTGTAGTCCCAGCTTCTCAGGAGACTGAGGCAGGAGAACCCAAGAGA A T SLIRP Ensembl:ENSG00000119705 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs944240895 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103903,RMVar_hsa_circ_88743,RMVar_hsa_circ_168212,RMVar_hsa_circ_168213 17638 RMVar_ID_17638 Human_SNP_ID_561583795 A-to-I Human chr14 + 77716891 77716891 77716891 TCAAGCGATTCTCCTGCCTCAACCTCCCGAGTAGCTGGGATTACAGGCATGCGCCACCACGCACT TCAAGCGATTCTCCTGCCTCAACCTCCCGAGTGGCTGGGATTACAGGCATGCGCCACCACGCACT A G SLIRP Ensembl:ENSG00000119705 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1341926089 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103903,RMVar_hsa_circ_88743,RMVar_hsa_circ_168212,RMVar_hsa_circ_168213 17639 RMVar_ID_17639 Human_SNP_ID_561583808 A-to-I Human chr14 + 77716927 77716927 77716927 GGGATTACAGGCATGCGCCACCACGCACTGCTAATTTTTTTTGTATTTTTAGTAGAGATTGGGTT GGGATTACAGGCATGCGCCACCACGCACTGCTGATTTTTTTTGTATTTTTAGTAGAGATTGGGTT A G SLIRP Ensembl:ENSG00000119705 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1456051489 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103903,RMVar_hsa_circ_88743,RMVar_hsa_circ_168212,RMVar_hsa_circ_168213 17640 RMVar_ID_17640 Human_SNP_ID_561583883 A-to-I Human chr14 + 77717179 77717179 77717179 TATTTTATTTTAAATTTTAGTTTTAATGAGACAGGGCCTTGCTATGTTGCAGGGTGGTGTTGAAC TATTTTATTTTAAATTTTAGTTTTAATGAGACGGGGCCTTGCTATGTTGCAGGGTGGTGTTGAAC A G SLIRP Ensembl:ENSG00000119705 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs931210710 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5112590,Human_RBP_ID_8410948,Human_RBP_ID_12431245,Human_RBP_ID_17562716,Human_RBP_ID_22473190 RMVar_hsa_circ_103903,RMVar_hsa_circ_88743,RMVar_hsa_circ_168212,RMVar_hsa_circ_168213 17641 RMVar_ID_17641 Human_SNP_ID_561584427 A-to-I Human chr14 - 77718875 77718875 77718875 GAAACTCTGTCTCTACTAAAAATACAAAAATTAGCTGGGTGTGGTGGCACATGCCTGTAATCCCA GAAACTCTGTCTCTACTAAAAATACAAAAATTGGCTGGGTGTGGTGGCACATGCCTGTAATCCCA T C SNW1 Ensembl:ENSG00000100603 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1433552494 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116577,RMVar_hsa_circ_112787,RMVar_hsa_circ_168217,RMVar_hsa_circ_168218 17642 RMVar_ID_17642 Human_SNP_ID_561584463 A-to-I Human chr14 - 77718981 77718981 77718981 TGAGCACAGGGAGGTCACAGCTCCAGTGAGCTATGTAGCACTTTGTGAGACCAAGGCAGGCGATC TGAGCACAGGGAGGTCACAGCTCCAGTGAGCTGTGTAGCACTTTGTGAGACCAAGGCAGGCGATC T C SNW1 Ensembl:ENSG00000100603 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs528060648 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116577,RMVar_hsa_circ_112787,RMVar_hsa_circ_168217,RMVar_hsa_circ_168218 17643 RMVar_ID_17643 Human_SNP_ID_561584489 A-to-I Human chr14 - 77719078 77719078 77719078 GCAATATGGCAAAACCCTGTCTACAAAAAATTAGCTGGACATGGTGGCACACACCTGTACTCCCA GCAATATGGCAAAACCCTGTCTACAAAAAATTGGCTGGACATGGTGGCACACACCTGTACTCCCA T C SNW1 Ensembl:ENSG00000100603 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1353484776 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116577,RMVar_hsa_circ_112787,RMVar_hsa_circ_168217,RMVar_hsa_circ_168218 17644 RMVar_ID_17644 Human_SNP_ID_561584510 A-to-I Human chr14 - 77719167 77719167 77719167 GCTGGGCACTGTGGCTCACGCCTGTAATCCTAACACTTTGTGAGACCTAGGCAGGCAGATTGCTT GCTGGGCACTGTGGCTCACGCCTGTAATCCTAGCACTTTGTGAGACCTAGGCAGGCAGATTGCTT T C SNW1 Ensembl:ENSG00000100603 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs176962 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_1278,GWAS_ID_1279,GWAS_ID_1280,GWAS_ID_1281,GWAS_ID_1282,GWAS_ID_1283,GWAS_ID_1284,GWAS_ID_1285,GWAS_ID_1286,GWAS_ID_1287,GWAS_ID_1288,GWAS_ID_1289,GWAS_ID_1290,GWAS_ID_1291,GWAS_ID_1292,GWAS_ID_1293,GWAS_ID_1294,GWAS_ID_1295,GWAS_ID_1296,GWAS_ID_1297,GWAS_ID_1298,GWAS_ID_1299,GWAS_ID_1300,GWAS_ID_1301,GWAS_ID_1302,GWAS_ID_1303,GWAS_ID_1304,GWAS_ID_1305,GWAS_ID_1306,GWAS_ID_1307,GWAS_ID_1308,GWAS_ID_1309,GWAS_ID_1310,GWAS_ID_1311,GWAS_ID_1312,GWAS_ID_1313,GWAS_ID_1314,GWAS_ID_1315,GWAS_ID_1316,GWAS_ID_1317,GWAS_ID_1318,GWAS_ID_1319,GWAS_ID_1320,GWAS_ID_1321,GWAS_ID_1322,GWAS_ID_1323,GWAS_ID_1324,GWAS_ID_1325,GWAS_ID_1326,GWAS_ID_1327,GWAS_ID_1328,GWAS_ID_1329,GWAS_ID_1330,GWAS_ID_1331,GWAS_ID_1332,GWAS_ID_1333,GWAS_ID_1334,GWAS_ID_1335,GWAS_ID_1336,GWAS_ID_1337,GWAS_ID_1338,GWAS_ID_1339,GWAS_ID_1340,GWAS_ID_1341,GWAS_ID_1342,GWAS_ID_1343,GWAS_ID_1344,GWAS_ID_1345,GWAS_ID_1346,GWAS_ID_1347,GWAS_ID_1348,GWAS_ID_1349,GWAS_ID_1350,GWAS_ID_1351,GWAS_ID_1352,GWAS_ID_1353,GWAS_ID_1354,GWAS_ID_1355,GWAS_ID_1356,GWAS_ID_1357,GWAS_ID_1358,GWAS_ID_1359,GWAS_ID_1360,GWAS_ID_1361,GWAS_ID_1362,GWAS_ID_1363,GWAS_ID_1364,GWAS_ID_1365,GWAS_ID_1366,GWAS_ID_1367,GWAS_ID_1368,GWAS_ID_1369,GWAS_ID_1370,GWAS_ID_1371,GWAS_ID_1372,GWAS_ID_1373,GWAS_ID_1374,GWAS_ID_1375,GWAS_ID_1376,GWAS_ID_1377,GWAS_ID_1378,GWAS_ID_1379,GWAS_ID_1380,GWAS_ID_1381,GWAS_ID_1382,GWAS_ID_1383,GWAS_ID_1384,GWAS_ID_1385,GWAS_ID_1386,GWAS_ID_1387,GWAS_ID_1388,GWAS_ID_1389,GWAS_ID_1390,GWAS_ID_1391,GWAS_ID_1392,GWAS_ID_1393,GWAS_ID_1394,GWAS_ID_1395,GWAS_ID_1396,GWAS_ID_1397,GWAS_ID_1398,GWAS_ID_1399,GWAS_ID_1400,GWAS_ID_1401,GWAS_ID_1402,GWAS_ID_1403,GWAS_ID_1404,GWAS_ID_1405,GWAS_ID_1406,GWAS_ID_1407,GWAS_ID_1408,GWAS_ID_1409,GWAS_ID_1410,GWAS_ID_1411,GWAS_ID_1412,GWAS_ID_1413,GWAS_ID_1414,GWAS_ID_1415,GWAS_ID_1416,GWAS_ID_1417,GWAS_ID_1418,GWAS_ID_1419,GWAS_ID_1420,GWAS_ID_1421,GWAS_ID_1422,GWAS_ID_1423,GWAS_ID_1424,GWAS_ID_1425,GWAS_ID_1426,GWAS_ID_1427,GWAS_ID_1428,GWAS_ID_1429,GWAS_ID_1430 RMVar_hsa_circ_116577,RMVar_hsa_circ_112787,RMVar_hsa_circ_168217,RMVar_hsa_circ_168218 17645 RMVar_ID_17645 Human_SNP_ID_561586497 A-to-I Human chr14 + 77726348 77726348 77726348 AAAATTTAATTTTTTTTCTTTTAAAAAGAGATAGGGTCTTACTGTGTTGCCCAGGGTGGTCTTGA AAAATTTAATTTTTTTTCTTTTAAAAAGAGATTGGGTCTTACTGTGTTGCCCAGGGTGGTCTTGA A T SLIRP Ensembl:ENSG00000119705 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1453909587 Functional Loss SNV dbSNP153 33..33 33 - - - 17646 RMVar_ID_17646 Human_SNP_ID_561588402 A-to-I Human chr14 - 77734589 77734588 77734589 GGACTACAGGCGCATGCCACCACGTCCGGCTAATTTTTCGTATTTTAGTAGAAACGGGGTTTCAC GGACTACAGGCGCATGCCACCACGTCCGGCTA_TTTTTCGTATTTTAGTAGAAACGGGGTTTCAC AT A SNW1 Ensembl:ENSG00000100603 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1231704150 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_116577,RMVar_hsa_circ_874,RMVar_hsa_circ_112787,RMVar_hsa_circ_168217,RMVar_hsa_circ_168218,RMVar_hsa_circ_326851,RMVar_hsa_circ_273379,RMVar_hsa_circ_168222,RMVar_hsa_circ_168219,RMVar_hsa_circ_168220,RMVar_hsa_circ_335743,RMVar_hsa_circ_341058,RMVar_hsa_circ_324703,RMVar_hsa_circ_301318,RMVar_hsa_circ_333060,RMVar_hsa_circ_291566,RMVar_hsa_circ_168223,RMVar_hsa_circ_334704,RMVar_hsa_circ_168224 17647 RMVar_ID_17647 Human_SNP_ID_561588403 A-to-I Human chr14 - 77734589 77734589 77734589 GGACTACAGGCGCATGCCACCACGTCCGGCTAATTTTTCGTATTTTAGTAGAAACGGGGTTTCAC GGACTACAGGCGCATGCCACCACGTCCGGCTAGTTTTTCGTATTTTAGTAGAAACGGGGTTTCAC T C SNW1 Ensembl:ENSG00000100603 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs530345555 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116577,RMVar_hsa_circ_874,RMVar_hsa_circ_112787,RMVar_hsa_circ_168217,RMVar_hsa_circ_168218,RMVar_hsa_circ_326851,RMVar_hsa_circ_273379,RMVar_hsa_circ_168222,RMVar_hsa_circ_168219,RMVar_hsa_circ_168220,RMVar_hsa_circ_335743,RMVar_hsa_circ_341058,RMVar_hsa_circ_324703,RMVar_hsa_circ_301318,RMVar_hsa_circ_333060,RMVar_hsa_circ_291566,RMVar_hsa_circ_168223,RMVar_hsa_circ_334704,RMVar_hsa_circ_168224 17648 RMVar_ID_17648 Human_SNP_ID_561588404 A-to-I Human chr14 - 77734589 77734589 77734589 GGACTACAGGCGCATGCCACCACGTCCGGCTAATTTTTCGTATTTTAGTAGAAACGGGGTTTCAC GGACTACAGGCGCATGCCACCACGTCCGGCTACTTTTTCGTATTTTAGTAGAAACGGGGTTTCAC T G SNW1 Ensembl:ENSG00000100603 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs530345555 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116577,RMVar_hsa_circ_874,RMVar_hsa_circ_112787,RMVar_hsa_circ_168217,RMVar_hsa_circ_168218,RMVar_hsa_circ_326851,RMVar_hsa_circ_273379,RMVar_hsa_circ_168222,RMVar_hsa_circ_168219,RMVar_hsa_circ_168220,RMVar_hsa_circ_335743,RMVar_hsa_circ_341058,RMVar_hsa_circ_324703,RMVar_hsa_circ_301318,RMVar_hsa_circ_333060,RMVar_hsa_circ_291566,RMVar_hsa_circ_168223,RMVar_hsa_circ_334704,RMVar_hsa_circ_168224 17649 RMVar_ID_17649 Human_SNP_ID_561593323 A-to-I Human chr14 - 77753464 77753464 77753464 TGTTGCTTTTGTTCTCTCTGATAGTGTTATTTATGGGAGGCAGAGGAAGATGAAAGATTATCAAG TGTTGCTTTTGTTCTCTCTGATAGTGTTATTTGTGGGAGGCAGAGGAAGATGAAAGATTATCAAG T C SNW1 Ensembl:ENSG00000100603 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs3783980 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_1431,GWAS_ID_1432,GWAS_ID_1433,GWAS_ID_1434,GWAS_ID_1435,GWAS_ID_1436,GWAS_ID_1437,GWAS_ID_1438,GWAS_ID_1439,GWAS_ID_1440,GWAS_ID_1441,GWAS_ID_1442,GWAS_ID_1443,GWAS_ID_1444,GWAS_ID_1445,GWAS_ID_1446,GWAS_ID_1447,GWAS_ID_1448,GWAS_ID_1449,GWAS_ID_1450,GWAS_ID_1451,GWAS_ID_1452,GWAS_ID_1453,GWAS_ID_1454,GWAS_ID_1455,GWAS_ID_1456,GWAS_ID_1457,GWAS_ID_1458,GWAS_ID_1459,GWAS_ID_1460,GWAS_ID_1461,GWAS_ID_1462,GWAS_ID_1463,GWAS_ID_1464,GWAS_ID_1465,GWAS_ID_1466,GWAS_ID_1467,GWAS_ID_1468,GWAS_ID_1469,GWAS_ID_1470,GWAS_ID_1471,GWAS_ID_1472,GWAS_ID_1473,GWAS_ID_1474,GWAS_ID_1475,GWAS_ID_1476,GWAS_ID_1477,GWAS_ID_1478,GWAS_ID_1479,GWAS_ID_1480,GWAS_ID_1481,GWAS_ID_1482,GWAS_ID_1483,GWAS_ID_1484,GWAS_ID_1485,GWAS_ID_1486,GWAS_ID_1487,GWAS_ID_1488,GWAS_ID_1489,GWAS_ID_1490,GWAS_ID_1491,GWAS_ID_1492,GWAS_ID_1493,GWAS_ID_1494,GWAS_ID_1495,GWAS_ID_1496,GWAS_ID_1497,GWAS_ID_1498,GWAS_ID_1499,GWAS_ID_1500,GWAS_ID_1501,GWAS_ID_1502,GWAS_ID_1503,GWAS_ID_1504,GWAS_ID_1505,GWAS_ID_1506,GWAS_ID_1507,GWAS_ID_1508,GWAS_ID_1509,GWAS_ID_1510,GWAS_ID_1511,GWAS_ID_1512,GWAS_ID_1513,GWAS_ID_1514,GWAS_ID_1515,GWAS_ID_1516,GWAS_ID_1517,GWAS_ID_1518,GWAS_ID_1519,GWAS_ID_1520,GWAS_ID_1521,GWAS_ID_1522,GWAS_ID_1523,GWAS_ID_1524,GWAS_ID_1525,GWAS_ID_1526,GWAS_ID_1527,GWAS_ID_1528,GWAS_ID_1529,GWAS_ID_1530,GWAS_ID_1531,GWAS_ID_1532,GWAS_ID_1533,GWAS_ID_1534,GWAS_ID_1535,GWAS_ID_1536,GWAS_ID_1537,GWAS_ID_1538,GWAS_ID_1539,GWAS_ID_1540,GWAS_ID_1541,GWAS_ID_1542,GWAS_ID_1543,GWAS_ID_1544,GWAS_ID_1545,GWAS_ID_1546,GWAS_ID_1547,GWAS_ID_1548,GWAS_ID_1549,GWAS_ID_1550,GWAS_ID_1551,GWAS_ID_1552,GWAS_ID_1553,GWAS_ID_1554,GWAS_ID_1555,GWAS_ID_1556,GWAS_ID_1557,GWAS_ID_1558,GWAS_ID_1559,GWAS_ID_1560,GWAS_ID_1561,GWAS_ID_1562,GWAS_ID_1563,GWAS_ID_1564,GWAS_ID_1565,GWAS_ID_1566,GWAS_ID_1567,GWAS_ID_1568,GWAS_ID_1569,GWAS_ID_1570,GWAS_ID_1571,GWAS_ID_1572,GWAS_ID_1573,GWAS_ID_1574,GWAS_ID_1575,GWAS_ID_1576,GWAS_ID_1577,GWAS_ID_1578,GWAS_ID_1579,GWAS_ID_1580,GWAS_ID_1581,GWAS_ID_1582,GWAS_ID_1583 RMVar_hsa_circ_74560 17650 RMVar_ID_17650 Human_SNP_ID_561594135 A-to-I Human chr14 - 77756840 77756840 77756840 AGTTTTGCTGTTGTTGCCTAGGCTGGAGTGCAATGGTGCAATCTTGGCTCACTGTACCCTCCACC AGTTTTGCTGTTGTTGCCTAGGCTGGAGTGCAGTGGTGCAATCTTGGCTCACTGTACCCTCCACC T C SNW1 Ensembl:ENSG00000100603 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs554967801 Functional Loss SNV dbSNP153 33..33 33 - - - 17651 RMVar_ID_17651 Human_SNP_ID_561755989 A-to-I Human chr14 + 78431916 78431916 78431916 CCCACTTTGCAGATGAGGAATCTAAGGCTCATAGGTCAGTAAGCCAGTAAAAGGCAGAGTTGGGA CCCACTTTGCAGATGAGGAATCTAAGGCTCATCGGTCAGTAAGCCAGTAAAAGGCAGAGTTGGGA A C NRXN3 Ensembl:ENSG00000021645 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs979660572 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9045699 17652 RMVar_ID_17652 Human_SNP_ID_561857903 A-to-I Human chr14 + 78866923 78866923 78866923 AGGTTCAAGCGATTCTCCTGCTTCAGCCTCCCAAGCAGCTGAGACTACAGGCACACACCACCATG AGGTTCAAGCGATTCTCCTGCTTCAGCCTCCCCAGCAGCTGAGACTACAGGCACACACCACCATG A C NRXN3 Ensembl:ENSG00000021645 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1245716157 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12943,RMVar_hsa_circ_296061,RMVar_hsa_circ_34964,RMVar_hsa_circ_23262 17653 RMVar_ID_17653 Human_SNP_ID_561861505 A-to-I Human chr14 + 78882286 78882286 78882286 CACACGGAGTCCCTACTGGGGTACTGACTAGTAGAACTGTGAGAAGAGGGCCACTGTCCTCCAGA CACACGGAGTCCCTACTGGGGTACTGACTAGTGGAACTGTGAGAAGAGGGCCACTGTCCTCCAGA A G NRXN3 Ensembl:ENSG00000021645 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1341085029 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12943,RMVar_hsa_circ_296061,RMVar_hsa_circ_34964,RMVar_hsa_circ_23262 17654 RMVar_ID_17654 Human_SNP_ID_561896241 A-to-I Human chr14 + 79023547 79023547 79023547 GGAGGTGTATTAGTCCATTCTCACACTGCTATAAAGAAATACCTGGGACTGGGTACTTTAAAAAG GGAGGTGTATTAGTCCATTCTCACACTGCTATGAAGAAATACCTGGGACTGGGTACTTTAAAAAG A G NRXN3 Ensembl:ENSG00000021645 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1045745433 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12943 17655 RMVar_ID_17655 Human_SNP_ID_561917687 A-to-I Human chr14 + 79112026 79112026 79112026 ACCAGAAGCCAAAAGAAGTTATAGTTTATTTTAAGCAATATCCACAAAACCTAATATAGTCCACT ACCAGAAGCCAAAAGAAGTTATAGTTTATTTTCAGCAATATCCACAAAACCTAATATAGTCCACT A C NRXN3 Ensembl:ENSG00000021645 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1245536077 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12943 17656 RMVar_ID_17656 Human_SNP_ID_561918323 A-to-I Human chr14 + 79114737 79114737 79114737 TTTTGGAGAGATGAGGACTTGCTATGTTGCTCAGGCTGGAATCAAACTCCTGGGCTCAAGCGATG TTTTGGAGAGATGAGGACTTGCTATGTTGCTCGGGCTGGAATCAAACTCCTGGGCTCAAGCGATG A G NRXN3 Ensembl:ENSG00000021645 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1323652640 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12943 17657 RMVar_ID_17657 Human_SNP_ID_561936661 A-to-I Human chr14 + 79188889 79188889 79188889 GAATGGCAATCATTAAAAAGTCAGGAAACAACAGGTGATGGAGAGGATGTGGAGAAATAGGAACA GAATGGCAATCATTAAAAAGTCAGGAAACAACGGGTGATGGAGAGGATGTGGAGAAATAGGAACA A G NRXN3 Ensembl:ENSG00000021645 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs996946125 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12943 17658 RMVar_ID_17658 Human_SNP_ID_561943755 A-to-I Human chr14 + 79219153 79219153 79219153 GTGGGCACTCAGTTTATTAGAGATAGGGTCTCACTCTGTGCCCCACGCTGGAATGCAGTTGGCAT GTGGGCACTCAGTTTATTAGAGATAGGGTCTCGCTCTGTGCCCCACGCTGGAATGCAGTTGGCAT A G NRXN3 Ensembl:ENSG00000021645 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs549915551 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12943 17659 RMVar_ID_17659 Human_SNP_ID_561963710 A-to-I Human chr14 + 79299198 79299198 79299198 TTACATTTTGAAAAGATACAGCACCATCCTATAAGATTTAAGCATCAACTTCTCAGCCTTGACCC TTACATTTTGAAAAGATACAGCACCATCCTATGAGATTTAAGCATCAACTTCTCAGCCTTGACCC A G NRXN3 Ensembl:ENSG00000021645 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs564973946 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12943 17660 RMVar_ID_17660 Human_SNP_ID_561964582 A-to-I Human chr14 + 79302771 79302771 79302771 CTGCCATGTAAGATATGCCTTGGTTTTCCCTCACCTTCTGCCATGATTGTAAGTTTCCTGAGGCT CTGCCATGTAAGATATGCCTTGGTTTTCCCTCGCCTTCTGCCATGATTGTAAGTTTCCTGAGGCT A G NRXN3 Ensembl:ENSG00000021645 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1223541307 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12943 17661 RMVar_ID_17661 Human_SNP_ID_561976455 A-to-I Human chr14 + 79352649 79352649 79352649 GTTTTAAAACAGAATAAAAATTAATTGGTGTTAGAAGCCAAGATTTCAGAGCTAGACCAATAATA GTTTTAAAACAGAATAAAAATTAATTGGTGTTGGAAGCCAAGATTTCAGAGCTAGACCAATAATA A G NRXN3 Ensembl:ENSG00000021645 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs994645394 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12943 17662 RMVar_ID_17662 Human_SNP_ID_562015146 A-to-I Human chr14 + 79508934 79508934 79508934 ATAATGCTAACCAAGCATGCTGGCTCATGCCTATAATCACAGCACTTTGGGAGGCAGAGGCGGGT ATAATGCTAACCAAGCATGCTGGCTCATGCCTGTAATCACAGCACTTTGGGAGGCAGAGGCGGGT A G NRXN3 Ensembl:ENSG00000021645 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs927364415 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_168259,RMVar_hsa_circ_12943,RMVar_hsa_circ_43797,RMVar_hsa_circ_309261,RMVar_hsa_circ_314637,RMVar_hsa_circ_285153,RMVar_hsa_circ_40727,RMVar_hsa_circ_168260,RMVar_hsa_circ_168258 17663 RMVar_ID_17663 Human_SNP_ID_562033341 A-to-I Human chr14 + 79585578 79585578 79585578 GTGGTGGTGTGTGCCTGTAGTCCCAGCTACTCAGGACGCTGAGGCAGGAGAATCGCCTGAACCCG GTGGTGGTGTGTGCCTGTAGTCCCAGCTACTCTGGACGCTGAGGCAGGAGAATCGCCTGAACCCG A T NRXN3 Ensembl:ENSG00000021645 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1296964110 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12943,RMVar_hsa_circ_43797,RMVar_hsa_circ_309261,RMVar_hsa_circ_314637,RMVar_hsa_circ_285153,RMVar_hsa_circ_40727 17664 RMVar_ID_17664 Human_SNP_ID_562033347 A-to-I Human chr14 + 79585591 79585591 79585591 CCTGTAGTCCCAGCTACTCAGGACGCTGAGGCAGGAGAATCGCCTGAACCCGGGAGGCGGAGGTT CCTGTAGTCCCAGCTACTCAGGACGCTGAGGCTGGAGAATCGCCTGAACCCGGGAGGCGGAGGTT A T NRXN3 Ensembl:ENSG00000021645 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1310777688 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12943,RMVar_hsa_circ_43797,RMVar_hsa_circ_309261,RMVar_hsa_circ_314637,RMVar_hsa_circ_285153,RMVar_hsa_circ_40727 17665 RMVar_ID_17665 Human_SNP_ID_562051271 A-to-I Human chr14 + 79662612 79662612 79662612 TATAAAGAAATACCTGAGAATGAGTGATTTATAAAGAAAAGAGTTTTTAATTGGCTCACAGTTCT TATAAAGAAATACCTGAGAATGAGTGATTTATGAAGAAAAGAGTTTTTAATTGGCTCACAGTTCT A G NRXN3 Ensembl:ENSG00000021645 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1425419003 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12943,RMVar_hsa_circ_43797,RMVar_hsa_circ_309261,RMVar_hsa_circ_314637,RMVar_hsa_circ_285153,RMVar_hsa_circ_40727 17666 RMVar_ID_17666 Human_SNP_ID_562051272 A-to-I Human chr14 + 79662612 79662612 79662612 TATAAAGAAATACCTGAGAATGAGTGATTTATAAAGAAAAGAGTTTTTAATTGGCTCACAGTTCT TATAAAGAAATACCTGAGAATGAGTGATTTATTAAGAAAAGAGTTTTTAATTGGCTCACAGTTCT A T NRXN3 Ensembl:ENSG00000021645 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1425419003 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12943,RMVar_hsa_circ_43797,RMVar_hsa_circ_309261,RMVar_hsa_circ_314637,RMVar_hsa_circ_285153,RMVar_hsa_circ_40727 17667 RMVar_ID_17667 Human_SNP_ID_562186640 A-to-I Human chr14 - 80197776 80197776 80197776 CGACTCAGTTAGTGGTTGGATGTAGTCACATTAGTTTGCCTCTCCCCATCTTTGTCTCCCTGGCA CGACTCAGTTAGTGGTTGGATGTAGTCACATTGGTTTGCCTCTCCCCATCTTTGTCTCCCTGGCA T C DIO2 Ensembl:ENSG00000211448 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1056813 Functional Loss SNV dbSNP153 33..33 33 - - - 17668 RMVar_ID_17668 Human_SNP_ID_562437158 A-to-I Human chr14 + 81246571 81246571 81246571 TGATCACGGCCTTTCGGTCGCACATGGTTACCATGGAGAAAGGGGCTGGCCAACTCCAACGGTCC TGATCACGGCCTTTCGGTCGCACATGGTTACCGTGGAGAAAGGGGCTGGCCAACTCCAACGGTCC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1189483865 Functional Loss SNV dbSNP153 33..33 33 - - - 17669 RMVar_ID_17669 Human_SNP_ID_562454310 A-to-I Human chr14 - 81318646 81318644 81318647 GGGTTTTACCATGTTGACCAGGCTGGTCTCAAACTCCTGACCTCAAGTGATCTGCCCGCCTCAGC GGGTTTTACCATGTTGACCAGGCTGGTCTCA___TCCTGACCTCAAGTGATCTGCCCGCCTCAGC AGTT A STON2 Ensembl:ENSG00000140022 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1454474498 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_117322,RMVar_hsa_circ_168305 17670 RMVar_ID_17670 Human_SNP_ID_562493762 A-to-I Human chr14 - 81480010 81480010 81480010 CTTGGAAATCTCTAGGTTAACAGTGTTAATGCATAGATATATGGCTGTATGCAGCATATCTACAC CTTGGAAATCTCTAGGTTAACAGTGTTAATGCGTAGATATATGGCTGTATGCAGCATATCTACAC T C SEL1L Ensembl:ENSG00000071537 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs12890754 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18927,RMVar_hsa_circ_288798,RMVar_hsa_circ_335053,RMVar_hsa_circ_168311 17671 RMVar_ID_17671 Human_SNP_ID_562601423 A-to-I Human chr14 - 81916672 81916672 81916672 ATTGCAATTGTTATAATAGGATTCAAACCTCTACTCCAAGGAAGGTCCCCCACTGACTTTGGCAT ATTGCAATTGTTATAATAGGATTCAAACCTCTGCTCCAAGGAAGGTCCCCCACTGACTTTGGCAT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878856575 Functional Loss SNV dbSNP153 33..33 33 - - - 17672 RMVar_ID_17672 Human_SNP_ID_562601458 A-to-I Human chr14 - 81916779 81916779 81916779 CTGAATGACTGAAACTGGTAGATGAACTCATCAATGATATCCTAGAGCCCCTGGTTGGGTAGTTC CTGAATGACTGAAACTGGTAGATGAACTCATCGATGATATCCTAGAGCCCCTGGTTGGGTAGTTC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs888945132 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5463602,Human_RBP_ID_5493980 17673 RMVar_ID_17673 Human_SNP_ID_563519163 A-to-I Human chr14 + 85543042 85543042 85543042 ATACAGATTCCTGGGCCAAGAAGAAGAACCTAAAGTCCAACTTCCTGTAACCATCAACACATTTA ATACAGATTCCTGGGCCAAGAAGAAGAACCTATAGTCCAACTTCCTGTAACCATCAACACATTTA A T FLRT2 Ensembl:ENSG00000185070 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1217836424 Functional Loss SNV dbSNP153 33..33 33 - - - 17674 RMVar_ID_17674 Human_SNP_ID_564290374 A-to-I Human chr14 + 88573131 88573131 88573131 GGCTGGGCACAGTGGCTCACACCTGTAATCCCAGGACTTTGGGAGGCCGAGGCGGGTGGATCACG GGCTGGGCACAGTGGCTCACACCTGTAATCCCGGGACTTTGGGAGGCCGAGGCGGGTGGATCACG A G ZC3H14 Ensembl:ENSG00000100722 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs933448093 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8391,RMVar_hsa_circ_36273,RMVar_hsa_circ_60189,RMVar_hsa_circ_63360,RMVar_hsa_circ_294022,RMVar_hsa_circ_47425,RMVar_hsa_circ_345678,RMVar_hsa_circ_168366,RMVar_hsa_circ_334794,RMVar_hsa_circ_15112,RMVar_hsa_circ_168367 17675 RMVar_ID_17675 Human_SNP_ID_564290494 A-to-I Human chr14 + 88573454 88573454 88573454 CAAATTTATTTTATTTTATTTTACTTTTTGAGAAGGAGTTTCACTCTTGTTGCCCAGGCTGGAGT CAAATTTATTTTATTTTATTTTACTTTTTGAGGAGGAGTTTCACTCTTGTTGCCCAGGCTGGAGT A G ZC3H14 Ensembl:ENSG00000100722 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs757792342 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2428838,Human_RBP_ID_12436140 RMVar_hsa_circ_8391,RMVar_hsa_circ_36273,RMVar_hsa_circ_60189,RMVar_hsa_circ_63360,RMVar_hsa_circ_294022,RMVar_hsa_circ_47425,RMVar_hsa_circ_345678,RMVar_hsa_circ_168366,RMVar_hsa_circ_334794,RMVar_hsa_circ_15112,RMVar_hsa_circ_168367 17676 RMVar_ID_17676 Human_SNP_ID_564290519 A-to-I Human chr14 + 88573533 88573533 88573533 TCAACTCACTGCAACCTCCACCTCCTGGGTTCAAGCGATTCTCCTGCTTCAGCCTCCCGAGTAGC TCAACTCACTGCAACCTCCACCTCCTGGGTTCGAGCGATTCTCCTGCTTCAGCCTCCCGAGTAGC A G ZC3H14 Ensembl:ENSG00000100722 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1427542182 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8391,RMVar_hsa_circ_36273,RMVar_hsa_circ_60189,RMVar_hsa_circ_63360,RMVar_hsa_circ_294022,RMVar_hsa_circ_47425,RMVar_hsa_circ_345678,RMVar_hsa_circ_168366,RMVar_hsa_circ_334794,RMVar_hsa_circ_15112,RMVar_hsa_circ_168367 17677 RMVar_ID_17677 Human_SNP_ID_564290550 A-to-I Human chr14 + 88573612 88573612 88573612 ACCATGCCTGGCTAATTTTTTGTATTTTTAGCAAAGACAGGGTTTCACCGTGTTGGCCAGGCTGG ACCATGCCTGGCTAATTTTTTGTATTTTTAGCGAAGACAGGGTTTCACCGTGTTGGCCAGGCTGG A G ZC3H14 Ensembl:ENSG00000100722 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs983725121 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1542864 RMVar_hsa_circ_8391,RMVar_hsa_circ_36273,RMVar_hsa_circ_60189,RMVar_hsa_circ_63360,RMVar_hsa_circ_294022,RMVar_hsa_circ_47425,RMVar_hsa_circ_345678,RMVar_hsa_circ_168366,RMVar_hsa_circ_334794,RMVar_hsa_circ_15112,RMVar_hsa_circ_168367 17678 RMVar_ID_17678 Human_SNP_ID_564290552 A-to-I Human chr14 + 88573618 88573617 88573619 CCTGGCTAATTTTTTGTATTTTTAGCAAAGACAGGGTTTCACCGTGTTGGCCAGGCTGGTCTTGA CCTGGCTAATTTTTTGTATTTTTAGCAAAGAC__GGTTTCACCGTGTTGGCCAGGCTGGTCTTGA CAG C ZC3H14 Ensembl:ENSG00000100722 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs928090631 Functional Loss DEL dbSNP153 33..34 33 - - - Human_Splice_Rec_1542864 RMVar_hsa_circ_8391,RMVar_hsa_circ_36273,RMVar_hsa_circ_60189,RMVar_hsa_circ_63360,RMVar_hsa_circ_294022,RMVar_hsa_circ_47425,RMVar_hsa_circ_345678,RMVar_hsa_circ_168366,RMVar_hsa_circ_334794,RMVar_hsa_circ_15112,RMVar_hsa_circ_168367 17679 RMVar_ID_17679 Human_SNP_ID_564290635 A-to-I Human chr14 + 88573901 88573901 88573901 GGCCTCCCAAAGTGTTGGGATTACAGGCATGTACCATGGCGCCTGGCCCCAAGTTTATTTTTAAA GGCCTCCCAAAGTGTTGGGATTACAGGCATGTGCCATGGCGCCTGGCCCCAAGTTTATTTTTAAA A G ZC3H14 Ensembl:ENSG00000100722 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs12434399 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_1584,GWAS_ID_1585,GWAS_ID_1586,GWAS_ID_1587 RMVar_hsa_circ_8391,RMVar_hsa_circ_36273,RMVar_hsa_circ_60189,RMVar_hsa_circ_63360,RMVar_hsa_circ_294022,RMVar_hsa_circ_47425,RMVar_hsa_circ_345678,RMVar_hsa_circ_168366,RMVar_hsa_circ_334794,RMVar_hsa_circ_15112,RMVar_hsa_circ_168367 17680 RMVar_ID_17680 Human_SNP_ID_564290816 A-to-I Human chr14 + 88574511 88574511 88574511 GTGATCCGCCCACTTCGGCCTTCCAAAGTGCTAGGATTACAGATGTGAGCCACCACACCCAGCCT GTGATCCGCCCACTTCGGCCTTCCAAAGTGCTGGGATTACAGATGTGAGCCACCACACCCAGCCT A G ZC3H14 Ensembl:ENSG00000100722 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,31158229,31158229,32596459 RNA-Seq:(High) rs929755545 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1543132,Human_Splice_Rec_1543133 RMVar_hsa_circ_8391,RMVar_hsa_circ_36273,RMVar_hsa_circ_60189,RMVar_hsa_circ_63360,RMVar_hsa_circ_294022,RMVar_hsa_circ_47425,RMVar_hsa_circ_345678,RMVar_hsa_circ_168366,RMVar_hsa_circ_334794,RMVar_hsa_circ_15112,RMVar_hsa_circ_168367 17681 RMVar_ID_17681 Human_SNP_ID_564294347 A-to-I Human chr14 + 88587446 88587446 88587446 CCTTGTCCTCCCAAAGTGCTGGGATTACAGGCATAAGCCACCATGCCAGGCCTCTCTTTCAAGTC CCTTGTCCTCCCAAAGTGCTGGGATTACAGGCCTAAGCCACCATGCCAGGCCTCTCTTTCAAGTC A C ZC3H14 Ensembl:ENSG00000100722 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1009708326 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17562608 RMVar_hsa_circ_63360,RMVar_hsa_circ_47425,RMVar_hsa_circ_4852,RMVar_hsa_circ_168372,RMVar_hsa_circ_323030,RMVar_hsa_circ_335301,RMVar_hsa_circ_343383,RMVar_hsa_circ_325556,RMVar_hsa_circ_311919,RMVar_hsa_circ_70886,RMVar_hsa_circ_168374,RMVar_hsa_circ_168375,RMVar_hsa_circ_168373,RMVar_hsa_circ_168371,RMVar_hsa_circ_280990,RMVar_hsa_circ_310658,RMVar_hsa_circ_64144,RMVar_hsa_circ_13241,RMVar_hsa_circ_168377 17682 RMVar_ID_17682 Human_SNP_ID_564294447 A-to-I Human chr14 + 88587831 88587831 88587831 TTTTAATTAGCTGGGTGTGATGATGTGCACCTATAGTCATGGCTACTCTGGAGAATTGCTTGAGC TTTTAATTAGCTGGGTGTGATGATGTGCACCTGTAGTCATGGCTACTCTGGAGAATTGCTTGAGC A G ZC3H14 Ensembl:ENSG00000100722 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917187919 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12436545 RMVar_hsa_circ_63360,RMVar_hsa_circ_47425,RMVar_hsa_circ_4852,RMVar_hsa_circ_168372,RMVar_hsa_circ_323030,RMVar_hsa_circ_335301,RMVar_hsa_circ_343383,RMVar_hsa_circ_325556,RMVar_hsa_circ_311919,RMVar_hsa_circ_70886,RMVar_hsa_circ_168374,RMVar_hsa_circ_168375,RMVar_hsa_circ_168373,RMVar_hsa_circ_168371,RMVar_hsa_circ_280990,RMVar_hsa_circ_310658,RMVar_hsa_circ_64144,RMVar_hsa_circ_13241 17683 RMVar_ID_17683 Human_SNP_ID_564297839 A-to-I Human chr14 + 88600726 88600725 88600727 CTTGTGCCTTGGCCTCCCAGAATGTTGGGATTACAGACATGAACCGCCACACCAGGCCACTTGAT CTTGTGCCTTGGCCTCCCAGAATGTTGGGATT__AGACATGAACCGCCACACCAGGCCACTTGAT TAC T ZC3H14 Ensembl:ENSG00000100722 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973958939 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_12436831 RMVar_hsa_circ_63360,RMVar_hsa_circ_4852,RMVar_hsa_circ_168372,RMVar_hsa_circ_335301,RMVar_hsa_circ_343383,RMVar_hsa_circ_325556,RMVar_hsa_circ_311919,RMVar_hsa_circ_70886,RMVar_hsa_circ_168374,RMVar_hsa_circ_168375,RMVar_hsa_circ_168373,RMVar_hsa_circ_280990,RMVar_hsa_circ_64144,RMVar_hsa_circ_7942,RMVar_hsa_circ_13241,RMVar_hsa_circ_16200 17684 RMVar_ID_17684 Human_SNP_ID_564301208 A-to-I Human chr14 + 88613645 88613645 88613645 TGTTGGATGACGTGGTTTAAAATGATCACCACAAAAAGGGACCACAAAAAAAGGAAGGAAATGAG TGTTGGATGACGTGGTTTAAAATGATCACCACCAAAAGGGACCACAAAAAAAGGAAGGAAATGAG A C ZC3H14 Ensembl:ENSG00000100722 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs963455014 Functional Loss SNV dbSNP153 33..33 33 - - - 17685 RMVar_ID_17685 Human_SNP_ID_564301209 A-to-I Human chr14 + 88613645 88613645 88613645 TGTTGGATGACGTGGTTTAAAATGATCACCACAAAAAGGGACCACAAAAAAAGGAAGGAAATGAG TGTTGGATGACGTGGTTTAAAATGATCACCACTAAAAGGGACCACAAAAAAAGGAAGGAAATGAG A T ZC3H14 Ensembl:ENSG00000100722 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs963455014 Functional Loss SNV dbSNP153 33..33 33 - - - 17686 RMVar_ID_17686 Human_SNP_ID_564302717 A-to-I Human chr14 - 88619109 88619109 88619109 TGCCCGCCTCCGCTTCCCAAAGTTCTGGGATTATAGGTGTGAGCCACTGGGCCTGGCCTAAGAAA TGCCCGCCTCCGCTTCCCAAAGTTCTGGGATTGTAGGTGTGAGCCACTGGGCCTGGCCTAAGAAA T C EML5 Ensembl:ENSG00000165521 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs952683807 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25117281 RMVar_hsa_circ_3938,RMVar_hsa_circ_267190,RMVar_hsa_circ_267320,RMVar_hsa_circ_31751,RMVar_hsa_circ_105861,RMVar_hsa_circ_168381 17687 RMVar_ID_17687 Human_SNP_ID_564304503 A-to-I Human chr14 - 88626377 88626376 88626377 AGCTATGTGATCCTCCCATCTTGACCTCCCAAAGTGCTGGGTTTACAGGCATGAGCCACCATAAT AGCTATGTGATCCTCCCATCTTGACCTCCCAA_GTGCTGGGTTTACAGGCATGAGCCACCATAAT CT C EML5 Ensembl:ENSG00000165521 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1242017662 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_267320,RMVar_hsa_circ_31751,RMVar_hsa_circ_28407,RMVar_hsa_circ_103052,RMVar_hsa_circ_105861,RMVar_hsa_circ_168381,RMVar_hsa_circ_265898,RMVar_hsa_circ_168382,RMVar_hsa_circ_66162 17688 RMVar_ID_17688 Human_SNP_ID_564328240 A-to-I Human chr14 - 88727310 88727310 88727310 CATCCCTTTGCACTGCTCCTCAGCTCATTACAAATTTCAGTGACACATTTACAACTTGACAGAAT CATCCCTTTGCACTGCTCCTCAGCTCATTACATATTTCAGTGACACATTTACAACTTGACAGAAT T A EML5 Ensembl:ENSG00000165521 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1367056265 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111661,RMVar_hsa_circ_103052,RMVar_hsa_circ_105861,RMVar_hsa_circ_168381,RMVar_hsa_circ_168382,RMVar_hsa_circ_374162,RMVar_hsa_circ_168387,RMVar_hsa_circ_102807,RMVar_hsa_circ_168389,RMVar_hsa_circ_121443,RMVar_hsa_circ_168392,RMVar_hsa_circ_168393,RMVar_hsa_circ_340889,RMVar_hsa_circ_329477,RMVar_hsa_circ_283825,RMVar_hsa_circ_168395,RMVar_hsa_circ_168396,RMVar_hsa_circ_168394,RMVar_hsa_circ_18161,RMVar_hsa_circ_104112,RMVar_hsa_circ_168407,RMVar_hsa_circ_330249,RMVar_hsa_circ_328860,RMVar_hsa_circ_293699,RMVar_hsa_circ_43192,RMVar_hsa_circ_168408,RMVar_hsa_circ_168409,RMVar_hsa_circ_337281,RMVar_hsa_circ_304590,RMVar_hsa_circ_377816,RMVar_hsa_circ_308599,RMVar_hsa_circ_301944,RMVar_hsa_circ_168417,RMVar_hsa_circ_168422,RMVar_hsa_circ_168418,RMVar_hsa_circ_377811,RMVar_hsa_circ_332854,RMVar_hsa_circ_168419,RMVar_hsa_circ_168421,RMVar_hsa_circ_344465,RMVar_hsa_circ_377259,RMVar_hsa_circ_330671,RMVar_hsa_circ_329653,RMVar_hsa_circ_168423,RMVar_hsa_circ_88482,RMVar_hsa_circ_307303,RMVar_hsa_circ_310626,RMVar_hsa_circ_168425,RMVar_hsa_circ_168426,RMVar_hsa_circ_313379,RMVar_hsa_circ_302889,RMVar_hsa_circ_168430,RMVar_hsa_circ_168427,RMVar_hsa_circ_168429,RMVar_hsa_circ_12787,RMVar_hsa_circ_168428,RMVar_hsa_circ_168432,RMVar_hsa_circ_284419,RMVar_hsa_circ_298537,RMVar_hsa_circ_168431 17689 RMVar_ID_17689 Human_SNP_ID_564456605 A-to-I Human chr14 - 89254632 89254632 89254632 GTACACAGATGGGTTTTTTTATTGTTGGACAGAGTGATTTTGAAAATTTGAATTCATTGCCACTA GTACACAGATGGGTTTTTTTATTGTTGGACAGGGTGATTTTGAAAATTTGAATTCATTGCCACTA T C FOXN3 Ensembl:ENSG00000053254 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1170429968 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_353413,RMVar_hsa_circ_45700 17690 RMVar_ID_17690 Human_SNP_ID_564468005 A-to-I Human chr14 - 89300961 89300961 89300961 CCGTCTCTACTAAAAAAAAAAGCAAAAAAATTAGCCGGGCATGGGGACAGGCACCTATAATCCCA CCGTCTCTACTAAAAAAAAAAGCAAAAAAATTGGCCGGGCATGGGGACAGGCACCTATAATCCCA T C FOXN3 Ensembl:ENSG00000053254 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1321747989 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_353413,RMVar_hsa_circ_45700,RMVar_hsa_circ_319601,RMVar_hsa_circ_335171,RMVar_hsa_circ_168457 17691 RMVar_ID_17691 Human_SNP_ID_564493574 A-to-I Human chr14 - 89392752 89392752 89392752 CCTGTAATCCCAGCTATTCAGGAGGCTGCGGCAGGAGAATTGCTTGAACCTGGGGGTCGGAGGTT CCTGTAATCCCAGCTATTCAGGAGGCTGCGGCGGGAGAATTGCTTGAACCTGGGGGTCGGAGGTT T C FOXN3 Ensembl:ENSG00000053254 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1163233333 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_319601,RMVar_hsa_circ_168457,RMVar_hsa_circ_343386 17692 RMVar_ID_17692 Human_SNP_ID_564539208 A-to-I Human chr14 - 89571361 89571361 89571361 GGGACTACAGGCGCCTGCTACCACGCTTGGCTAATTTTTGTATTTTTAGTAGAGGTGGGATTTCA GGGACTACAGGCGCCTGCTACCACGCTTGGCTGATTTTTGTATTTTTAGTAGAGGTGGGATTTCA T C AL137230.3,FOXN3 Ensembl:ENSG00000259053,Ensembl:ENSG00000053254 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs369695871 Functional Loss SNV dbSNP153 33..33 33 - - - 17693 RMVar_ID_17693 Human_SNP_ID_564544482 A-to-I Human chr14 - 89594804 89594804 89594804 TCGACTCACTGCAGCCTCTGCCTCCCGGATTCAGGTGATTCTCCTGCTCCAGCCTCCCAAGTAGC TCGACTCACTGCAGCCTCTGCCTCCCGGATTCGGGTGATTCTCCTGCTCCAGCCTCCCAAGTAGC T C AL137230.3,FOXN3 Ensembl:ENSG00000259053,Ensembl:ENSG00000053254 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1303488685 Functional Loss SNV dbSNP153 33..33 33 - - - 17694 RMVar_ID_17694 Human_SNP_ID_564590988 A-to-I Human chr14 - 89795580 89795580 89795580 TCACTGCAACTTCCGCCTCCTGGGATCAAGTGATTCTCCTGCCTTAGCCTCCTGAGTATCTGGGT TCACTGCAACTTCCGCCTCCTGGGATCAAGTGGTTCTCCTGCCTTAGCCTCCTGAGTATCTGGGT T C AL137230.3,EFCAB11 Ensembl:ENSG00000259053,Ensembl:ENSG00000140025 lincRNA,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1478766485 Functional Loss SNV dbSNP153 33..33 33 - - - 17695 RMVar_ID_17695 Human_SNP_ID_564590989 A-to-I Human chr14 - 89795584 89795584 89795584 CGGCTCACTGCAACTTCCGCCTCCTGGGATCAAGTGATTCTCCTGCCTTAGCCTCCTGAGTATCT CGGCTCACTGCAACTTCCGCCTCCTGGGATCAGGTGATTCTCCTGCCTTAGCCTCCTGAGTATCT T C AL137230.3,EFCAB11 Ensembl:ENSG00000259053,Ensembl:ENSG00000140025 lincRNA,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1466728248 Functional Loss SNV dbSNP153 33..33 33 - - - 17696 RMVar_ID_17696 Human_SNP_ID_564591173 A-to-I Human chr14 - 89796336 89796336 89796336 CACTGTCGCACTCCAGCCTGGATGATAGAGCAAGACCCTGTCTCTAAAAAAACACTTTCAATTAA CACTGTCGCACTCCAGCCTGGATGATAGAGCAGGACCCTGTCTCTAAAAAAACACTTTCAATTAA T C AL137230.3,EFCAB11 Ensembl:ENSG00000259053,Ensembl:ENSG00000140025 lincRNA,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs896695068 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_473761,Human_miRNA_ID_1264609 17697 RMVar_ID_17697 Human_SNP_ID_326426102 A-to-I Human chr7 - 75067262 75067262 75067262 AGTCTCGCTCTTGTCCCCCAGGCTGAAGTGCAATGGCGCAATCTCAGCTCACTGCAACCTCCGCC AGTCTCGCTCTTGTCCCCCAGGCTGAAGTGCAGTGGCGCAATCTCAGCTCACTGCAACCTCCGCC T C RCC1L Ensembl:ENSG00000274523 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs587767746 Functional Loss SNV dbSNP153 33..33 33 - - - 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 17698 RMVar_ID_17698 Human_SNP_ID_326427746 A-to-I Human chr7 - 75072735 75072734 75072735 ACTCAAGCGATCCGCCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGTGCC ACTCAAGCGATCCGCCCGCCTTGGCCTCCCAA_GTGCTGGGATTACAGGCGTGAGCCACTGTGCC CT C RCC1L Ensembl:ENSG00000274523 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs35229511 Functional Loss DEL dbSNP153 33..33 33 - - - 17699 RMVar_ID_17699 Human_SNP_ID_326443582 A-to-I Human chr7 + 75146458 75146458 75146458 TCACACCTATAATCCCAGGACTTTTGGAGGCCAAGGCAAGAGGATTGCTTGAGGCCAGGAGTTTG TCACACCTATAATCCCAGGACTTTTGGAGGCCCAGGCAAGAGGATTGCTTGAGGCCAGGAGTTTG A C GTF2IRD2B Ensembl:ENSG00000174428 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1554454298 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_877752,Human_Splice_Rec_877782 17700 RMVar_ID_17700 Human_SNP_ID_326463672 A-to-I Human chr7 + 75365585 75365585 75365585 CCTTTCTGCAGGACTGGATGGTTTCCATGATCATGGACAGAGAGTACAGTGTGGCAGTGGAGGCC CCTTTCTGCAGGACTGGATGGTTTCCATGATCGTGGACAGAGAGTACAGTGTGGCAGTGGAGGCC A G STAG3L1 Ensembl:ENSG00000205583 Pseudogene exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs236600 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5623819,Human_RBP_ID_17428735 Human_Splice_Rec_878102,Human_Splice_Rec_878103,Human_Splice_Rec_878114,Human_Splice_Rec_878115 RMVar_hsa_circ_245737,RMVar_hsa_circ_287936,RMVar_hsa_circ_337340,RMVar_hsa_circ_339097,RMVar_hsa_circ_336398 17701 RMVar_ID_17701 Human_SNP_ID_326464013 A-to-I Human chr7 + 75368231 75368231 75368231 GTGGTGGTGCATGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACCCG GTGGTGGTGCATGCCTGTAATCCCAGCTACTCTGGAGGCTGAGGCAGGAGAATCGCTTGAACCCG A T STAG3L1 Ensembl:ENSG00000205583 Pseudogene intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1177862778 Functional Loss SNV dbSNP153 33..33 33 - - - 17702 RMVar_ID_17702 Human_SNP_ID_326464419 A-to-I Human chr7 + 75369852 75369852 75369852 GCTGGAGTGCAGTGGCAGTTCTCAGCTCACCGAAACCTCTGCCTCCCGGGCTCAAGCAATTCTCA GCTGGAGTGCAGTGGCAGTTCTCAGCTCACCGCAACCTCTGCCTCCCGGGCTCAAGCAATTCTCA A C STAG3L1 Ensembl:ENSG00000205583 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1224222051 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18409728 17703 RMVar_ID_17703 Human_SNP_ID_326464808 A-to-I Human chr7 + 75372695 75372695 75372695 GAACACCTGAACTCAGGTGATCTGCCCACCTCAGCCTCCCAAAGGGCTGGGATTACAGGTGTAAT GAACACCTGAACTCAGGTGATCTGCCCACCTCGGCCTCCCAAAGGGCTGGGATTACAGGTGTAAT A G STAG3L1 Ensembl:ENSG00000205583 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1254638943 Functional Loss SNV dbSNP153 33..33 33 - - - 17704 RMVar_ID_17704 Human_SNP_ID_326466631 A-to-I Human chr7 - 75384508 75384508 75384508 CTGGAAACAGGTCCCCACCACTGCTCTGCCCCAGAAGGAAGGCTGGGCTGCTTCCCTTTGAGCTC CTGGAAACAGGTCCCCACCACTGCTCTGCCCCGGAAGGAAGGCTGGGCTGCTTCCCTTTGAGCTC T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs782801552 Functional Loss SNV dbSNP153 33..33 33 - - - 17705 RMVar_ID_17705 Human_SNP_ID_326470523 A-to-I Human chr7 - 75410779 75410779 75410779 CCAGTCCCGCCGTGCACGGCAGCGGGGCTGAAACCAGATGACAAAGCGCTGACCGTCGGGGTTCA CCAGTCCCGCCGTGCACGGCAGCGGGGCTGAACCCAGATGACAAAGCGCTGACCGTCGGGGTTCA T G - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs797026271 Functional Loss SNV dbSNP153 33..33 33 - - - 17706 RMVar_ID_17706 Human_SNP_ID_326472614 A-to-I Human chr7 - 75418732 75418726 75418733 CTTCCCTAAATCTGGACCTTGGCACGTGCTAGAAAGAGCCTTGGACCCTTCCAGCTGCGTAAAGC CTTCCCTAAATCTGGACCTTGGCACGTGCTA_______CCTTGGACCCTTCCAGCTGCGTAAAGC GCTCTTTC G POM121C Ensembl:ENSG00000272391 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1470387215 Functional Loss DEL dbSNP153 32..38 33 - - - 17707 RMVar_ID_17707 Human_SNP_ID_326472617 A-to-I Human chr7 - 75418732 75418732 75418732 CTTCCCTAAATCTGGACCTTGGCACGTGCTAGAAAGAGCCTTGGACCCTTCCAGCTGCGTAAAGC CTTCCCTAAATCTGGACCTTGGCACGTGCTAGGAAGAGCCTTGGACCCTTCCAGCTGCGTAAAGC T C POM121C Ensembl:ENSG00000272391 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs3973308 Functional Loss SNV dbSNP153 33..33 33 - - - 17708 RMVar_ID_17708 Human_SNP_ID_326475765 A-to-I Human chr7 - 75428817 75428817 75428817 CACCACCACACCTGGCTAATTTTTGTATTTCTAGTAGAGATGAGGTTTCACCATGTTGGCCACAC CACCACCACACCTGGCTAATTTTTGTATTTCTGGTAGAGATGAGGTTTCACCATGTTGGCCACAC T C POM121C Ensembl:ENSG00000272391 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1296880210 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2540,RMVar_hsa_circ_8579,RMVar_hsa_circ_310362 17709 RMVar_ID_17709 Human_SNP_ID_326476852 A-to-I Human chr7 - 75433111 75433111 75433111 CTTGCCTCAGCCTCCCAAGTAGTTGGGATTACAGGCTCTGGCCACCACGCCCAGCTAATTTTTTG CTTGCCTCAGCCTCCCAAGTAGTTGGGATTACTGGCTCTGGCCACCACGCCCAGCTAATTTTTTG T A POM121C Ensembl:ENSG00000272391 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1236338577 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2540,RMVar_hsa_circ_8579,RMVar_hsa_circ_310362 17710 RMVar_ID_17710 Human_SNP_ID_326481100 A-to-I Human chr7 - 75448787 75448787 75448787 TATTTGGTTTTTTTTTTTTGAGACAGAGTTTCACTCTTGTTGCCCAGGCTGGAGTGCAGTGGCGC TATTTGGTTTTTTTTTTTTGAGACAGAGTTTCTCTCTTGTTGCCCAGGCTGGAGTGCAGTGGCGC T A POM121C Ensembl:ENSG00000272391 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1554475214 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45327 17711 RMVar_ID_17711 Human_SNP_ID_326481138 A-to-I Human chr7 - 75448951 75448951 75448951 ACACCACTGCATTCCAGCCTGGGCAACAGAGCAAGATCCTGTCTCTTAAAAAACATTGCCACAAA ACACCACTGCATTCCAGCCTGGGCAACAGAGCCAGATCCTGTCTCTTAAAAAACATTGCCACAAA T G POM121C Ensembl:ENSG00000272391 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1242656144 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45327 17712 RMVar_ID_17712 Human_SNP_ID_326481329 A-to-I Human chr7 - 75449646 75449644 75449646 TTCCCCTACTGTTGCCGGGCATGGTAGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGCGGG TTCCCCTACTGTTGCCGGGCATGGTAGCTCAC__CTGTAATCCCAGCACTTTGGGAGGCTGCGGG GGT G POM121C Ensembl:ENSG00000272391 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1415366174 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_45327 17713 RMVar_ID_17713 Human_SNP_ID_326484058 A-to-I Human chr7 - 75461489 75461489 75461489 ATTGCTTGAACCCAGGAGGCGGAGGTTGCAGTAAGCCGATTGCACCTCTGCACTCCAGCCTGGGC ATTGCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCCGATTGCACCTCTGCACTCCAGCCTGGGC T C POM121C Ensembl:ENSG00000272391 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1260220215 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26139105 RMVar_hsa_circ_45327 17714 RMVar_ID_17714 Human_SNP_ID_326484627 A-to-I Human chr7 - 75463849 75463849 75463849 CATCTCTACTAAAAATCCAAAAACAGTCAGACATGGTAGCATGCCCCTATAATCCCAGCTACTCA CATCTCTACTAAAAATCCAAAAACAGTCAGACGTGGTAGCATGCCCCTATAATCCCAGCTACTCA T C POM121C Ensembl:ENSG00000272391 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1168721963 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45327 17715 RMVar_ID_17715 Human_SNP_ID_326484991 A-to-I Human chr7 - 75465173 75465173 75465173 CTGGCCAACATGGTGAAACCCCAATCTCTACTAAAAATACAAAAATAGCCGGGCATGGTGGCGCA CTGGCCAACATGGTGAAACCCCAATCTCTACTGAAAATACAAAAATAGCCGGGCATGGTGGCGCA T C POM121C Ensembl:ENSG00000272391 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1214547984 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45327 17716 RMVar_ID_17716 Human_SNP_ID_326485106 A-to-I Human chr7 - 75465590 75465590 75465590 TGCCACCATGCCCGGCTAATTTTTGTCTTTTCAGTAGAGACGGGGTTTCACCATCTTGGCCAGGC TGCCACCATGCCCGGCTAATTTTTGTCTTTTCGGTAGAGACGGGGTTTCACCATCTTGGCCAGGC T C POM121C Ensembl:ENSG00000272391 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1469195413 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45327 17717 RMVar_ID_17717 Human_SNP_ID_326485747 A-to-I Human chr7 - 75468049 75468049 75468049 CAGCTCACTGCAACTTCTGCCTCCTCAGTTCAAGCAATTCTCCGGCCTCAGCCCCTGAGTAGCTG CAGCTCACTGCAACTTCTGCCTCCTCAGTTCAGGCAATTCTCCGGCCTCAGCCCCTGAGTAGCTG T C POM121C Ensembl:ENSG00000272391 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1380789567 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45327 17718 RMVar_ID_17718 Human_SNP_ID_326485748 A-to-I Human chr7 - 75468049 75468049 75468049 CAGCTCACTGCAACTTCTGCCTCCTCAGTTCAAGCAATTCTCCGGCCTCAGCCCCTGAGTAGCTG CAGCTCACTGCAACTTCTGCCTCCTCAGTTCACGCAATTCTCCGGCCTCAGCCCCTGAGTAGCTG T G POM121C Ensembl:ENSG00000272391 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1380789567 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45327 17719 RMVar_ID_17719 Human_SNP_ID_326487287 A-to-I Human chr7 - 75474372 75474372 75474372 TTTGGTTTTTGGAGACGGAGTCTTGTTCTGTCACCCAGGCTGATGTGCACTGGTATGATCTCAGC TTTGGTTTTTGGAGACGGAGTCTTGTTCTGTCGCCCAGGCTGATGTGCACTGGTATGATCTCAGC T C POM121C Ensembl:ENSG00000272391 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs55818051 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45327 17720 RMVar_ID_17720 Human_SNP_ID_326487417 A-to-I Human chr7 - 75474884 75474884 75474884 ATAAGGTAAAAAATGGAGCATTTCTGTTATGCAGCTTATGAGGTGGCAACATCTTGTACTTCGGA ATAAGGTAAAAAATGGAGCATTTCTGTTATGCGGCTTATGAGGTGGCAACATCTTGTACTTCGGA T C AC211429.2,POM121C Ensembl:ENSG00000242073,Ensembl:ENSG00000272391 Pseudogene,Protein coding intron,intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1359280495 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9403511 RMVar_hsa_circ_45327,RMVar_hsa_circ_245743,RMVar_hsa_circ_306137 17721 RMVar_ID_17721 Human_SNP_ID_326491150 A-to-I Human chr7 - 75488665 75488665 75488665 CCTCAGCCTCCCAAGTATCTGGGACTACAGGCACGCACCACCGCACCCGGCTAATTTTTTGTGTT CCTCAGCCTCCCAAGTATCTGGGACTACAGGCGCGCACCACCGCACCCGGCTAATTTTTTGTGTT T C RF00017-4673 RNACentral:URS000091B0E9 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1318005768 Functional Loss SNV dbSNP153 33..33 33 - - - 17722 RMVar_ID_17722 Human_SNP_ID_326500351 A-to-I Human chr7 - 75518542 75518542 75518542 CTCCTGCCTCAGCTTCCCGAGTAGCTGGGACCACAGGCACCCGCCGCCATGCCCGGCTAATGTTT CTCCTGCCTCAGCTTCCCGAGTAGCTGGGACCGCAGGCACCCGCCGCCATGCCCGGCTAATGTTT T C PMS2P3 Ensembl:ENSG00000127957 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1554486078 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57016,RMVar_hsa_circ_73661,RMVar_hsa_circ_362944,RMVar_hsa_circ_74320 17723 RMVar_ID_17723 Human_SNP_ID_326513362 A-to-I Human chr7 - 75569487 75569487 75569487 CTCCCACCTCAACCTCTTGAGTAGCTAAGACTACAGTGCACATCACCACACCTGGCTAATTTTTA CTCCCACCTCAACCTCTTGAGTAGCTAAGACTGCAGTGCACATCACCACACCTGGCTAATTTTTA T C HIP1 Ensembl:ENSG00000127946 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs782070326 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12365,RMVar_hsa_circ_70071,RMVar_hsa_circ_319790,RMVar_hsa_circ_335968,RMVar_hsa_circ_303603,RMVar_hsa_circ_312025,RMVar_hsa_circ_272064,RMVar_hsa_circ_37798,RMVar_hsa_circ_297869,RMVar_hsa_circ_317008,RMVar_hsa_circ_35582,RMVar_hsa_circ_270749 17724 RMVar_ID_17724 Human_SNP_ID_326523511 A-to-I Human chr7 - 75608186 75608186 75608186 TTTCTGCCTCAGCCTTCCGAGCAGCTGGGATTACAGGTGCCCACCACCACGCCCGGCTAATTTTT TTTCTGCCTCAGCCTTCCGAGCAGCTGGGATTGCAGGTGCCCACCACCACGCCCGGCTAATTTTT T C HIP1 Ensembl:ENSG00000127946 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs782235598 Functional Loss SNV dbSNP153 33..33 33 - - - 17725 RMVar_ID_17725 Human_SNP_ID_326529602 A-to-I Human chr7 - 75632670 75632669 75632670 AAATTGGCCAGGCACAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGTTGAGGCAGGAGGA AAATTGGCCAGGCACAGTGGCTCACACCTGTA_TCCCAGCACTTTGGGAGGTTGAGGCAGGAGGA AT A HIP1 Ensembl:ENSG00000127946 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1217511414 Functional Loss DEL dbSNP153 33..33 33 - - - 17726 RMVar_ID_17726 Human_SNP_ID_326529604 A-to-I Human chr7 - 75632677 75632677 75632677 AGAATGGAAATTGGCCAGGCACAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGTTGAGGC AGAATGGAAATTGGCCAGGCACAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGTTGAGGC T C HIP1 Ensembl:ENSG00000127946 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs979762109 Functional Loss SNV dbSNP153 33..33 33 - - - 17727 RMVar_ID_17727 Human_SNP_ID_326538586 A-to-I Human chr7 - 75665176 75665171 75665176 CTCACTGTAGCCTCCAACTCCTGGCCTCAAACAATCCTCCTCCCTCAACCCCCTGACTAGCTGGG CTCACTGTAGCCTCCAACTCCTGGCCTCAAAC_____TCCTCCCTCAACCCCCTGACTAGCTGGG AGGATT A HIP1 Ensembl:ENSG00000127946 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1295497301 Functional Loss DEL dbSNP153 33..37 33 - - - 17728 RMVar_ID_17728 Human_SNP_ID_326547378 A-to-I Human chr7 - 75700829 75700829 75700829 TGGTGGCGGGTGCCTGTAGTCCCAGCTACTCAAGAGGCTGAGGCAGGAGAATGGCGTGAACCCGG TGGTGGCGGGTGCCTGTAGTCCCAGCTACTCATGAGGCTGAGGCAGGAGAATGGCGTGAACCCGG T A HIP1 Ensembl:ENSG00000127946 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs928909280 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_174536 17729 RMVar_ID_17729 Human_SNP_ID_326547379 A-to-I Human chr7 - 75700829 75700829 75700829 TGGTGGCGGGTGCCTGTAGTCCCAGCTACTCAAGAGGCTGAGGCAGGAGAATGGCGTGAACCCGG TGGTGGCGGGTGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATGGCGTGAACCCGG T C HIP1 Ensembl:ENSG00000127946 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs928909280 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_174536 17730 RMVar_ID_17730 Human_SNP_ID_326547423 A-to-I Human chr7 - 75700964 75700964 75700964 GTGGTGGCTCACGCCTGTAGTCCCAGCACTTTAGGAGGCCGAGACGGGCGGATCACGAGGTCAGG GTGGTGGCTCACGCCTGTAGTCCCAGCACTTTGGGAGGCCGAGACGGGCGGATCACGAGGTCAGG T C HIP1 Ensembl:ENSG00000127946 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs200894507 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_174536 17731 RMVar_ID_17731 Human_SNP_ID_326551673 A-to-I Human chr7 - 75719444 75719444 75719444 TCTGGAGTGCAGCGGCATGATCTCGGTTCACTACAAACTCCACCTTCCGGGTTCCCGCCATTCTC TCTGGAGTGCAGCGGCATGATCTCGGTTCACTGCAAACTCCACCTTCCGGGTTCCCGCCATTCTC T C HIP1 Ensembl:ENSG00000127946 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1563311944 Functional Loss SNV dbSNP153 33..33 33 - - - 17732 RMVar_ID_17732 Human_SNP_ID_326552324 A-to-I Human chr7 - 75722224 75722224 75722224 TTCACTGCAGCCTCAAACTCCTGGGCTCCAGCAATCCTCCCACCTCAGCCTCGCAAGTAGCTGGG TTCACTGCAGCCTCAAACTCCTGGGCTCCAGCCATCCTCCCACCTCAGCCTCGCAAGTAGCTGGG T G HIP1 Ensembl:ENSG00000127946 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1554521592 Functional Loss SNV dbSNP153 33..33 33 - - - 17733 RMVar_ID_17733 Human_SNP_ID_326555611 A-to-I Human chr7 - 75735884 75735884 75735884 TAAAGAAAAAGAACCAGCCTGGACAACATAGTAAGACCCCATCTCTACAAAAAATAAAATTAGCT TAAAGAAAAAGAACCAGCCTGGACAACATAGTGAGACCCCATCTCTACAAAAAATAAAATTAGCT T C HIP1 Ensembl:ENSG00000127946 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017710794 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16219646 17734 RMVar_ID_17734 Human_SNP_ID_326596619 A-to-I Human chr7 + 75882350 75882349 75882351 AAAATTGGGCTTACTTTGTATTTTTTCGAAACAGAGTCTCTGTCACCCAGGCTGGAGTGCAGTGG AAAATTGGGCTTACTTTGTATTTTTTCGAAAC__AGTCTCTGTCACCCAGGCTGGAGTGCAGTGG CAG C RHBDD2 Ensembl:ENSG00000005486 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1563377017 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_16219694 RMVar_hsa_circ_288654,RMVar_hsa_circ_333207 17735 RMVar_ID_17735 Human_SNP_ID_326596657 A-to-I Human chr7 + 75882534 75882534 75882534 TTTAGTAGACACAGGGTTTCACCATGTTGCCCAGGCTGGTCTTGAACTCCTGGTCTCAGGTGATC TTTAGTAGACACAGGGTTTCACCATGTTGCCCTGGCTGGTCTTGAACTCCTGGTCTCAGGTGATC A T RHBDD2 Ensembl:ENSG00000005486 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs933883846 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_288654,RMVar_hsa_circ_333207 17736 RMVar_ID_17736 Human_SNP_ID_326597139 A-to-I Human chr7 + 75884299 75884299 75884299 GCTGGATTGCAGTGGTATGATCATAGCCCGCTACAGCCTCACACTCGTGGACTCAAGTGATCCTC GCTGGATTGCAGTGGTATGATCATAGCCCGCTGCAGCCTCACACTCGTGGACTCAAGTGATCCTC A G RHBDD2 Ensembl:ENSG00000005486 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs782296698 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22325622 RMVar_hsa_circ_122849,RMVar_hsa_circ_245760 17737 RMVar_ID_17737 Human_SNP_ID_326607627 A-to-I Human chr7 + 75924465 75924465 75924465 GCACTGTGGGAGGCCGAGGTGGACGGATCACTAGAGCCCAGGAATTCAAGACCATCCTGGGCCAC GCACTGTGGGAGGCCGAGGTGGACGGATCACTGGAGCCCAGGAATTCAAGACCATCCTGGGCCAC A G POR Ensembl:ENSG00000127948 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1399256245 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17577456 17738 RMVar_ID_17738 Human_SNP_ID_326608037 A-to-I Human chr7 + 75926217 75926217 75926217 TGGGGTCTTGCTATGTTGCCCAGGCCGATCTCAAACTCCTGGGCTCAAACGATCCTCCTGTTGAC TGGGGTCTTGCTATGTTGCCCAGGCCGATCTCGAACTCCTGGGCTCAAACGATCCTCCTGTTGAC A G POR Ensembl:ENSG00000127948 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs782756069 Functional Loss SNV dbSNP153 33..33 33 - - - 17739 RMVar_ID_17739 Human_SNP_ID_326609124 A-to-I Human chr7 + 75930414 75930414 75930414 TGAGGTGGGAGGATCACTTGATCCTGGGAGGTAGAGGTTGTGGTGACCTATGATTGCACCACTGC TGAGGTGGGAGGATCACTTGATCCTGGGAGGTGGAGGTTGTGGTGACCTATGATTGCACCACTGC A G POR Ensembl:ENSG00000127948 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264121891 Functional Loss SNV dbSNP153 33..33 33 - - - 17740 RMVar_ID_17740 Human_SNP_ID_326609390 A-to-I Human chr7 + 75931415 75931415 75931415 TTGAGACACAGTCTCCCTCTCTCACGCAGGCTATAATGCAGTGGTGCAGTCTTGGCTCACTGCAA TTGAGACACAGTCTCCCTCTCTCACGCAGGCTCTAATGCAGTGGTGCAGTCTTGGCTCACTGCAA A C POR Ensembl:ENSG00000127948 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1407058549 Functional Loss SNV dbSNP153 33..33 33 - - - 17741 RMVar_ID_17741 Human_SNP_ID_326611710 A-to-I Human chr7 + 75939807 75939807 75939807 TTTTTGTATTTTTAGTAGAGACTGGGTTTCCCAATGTTGGCCAGGCTGGTCTCGAGCTCCTGACC TTTTTGTATTTTTAGTAGAGACTGGGTTTCCCGATGTTGGCCAGGCTGGTCTCGAGCTCCTGACC A G POR Ensembl:ENSG00000127948 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1380404695 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16220206 17742 RMVar_ID_17742 Human_SNP_ID_326612717 A-to-I Human chr7 + 75944337 75944337 75944337 TCACTTGAGGCCAGGAGTTTGAGACCAGCCCCAGCAACATGGTGAGACCCTGTCTTTACTAAAAA TCACTTGAGGCCAGGAGTTTGAGACCAGCCCCGGCAACATGGTGAGACCCTGTCTTTACTAAAAA A G POR Ensembl:ENSG00000127948 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1354505971 Functional Loss SNV dbSNP153 33..33 33 - - - 17743 RMVar_ID_17743 Human_SNP_ID_326612882 A-to-I Human chr7 + 75945127 75945127 75945127 ATGTGGCAAAACCCTGTCTCTACTAAAAATACAAAAATTAGCCAGGTGTGGTGAGGCACACCTGT ATGTGGCAAAACCCTGTCTCTACTAAAAATACTAAAATTAGCCAGGTGTGGTGAGGCACACCTGT A T POR Ensembl:ENSG00000127948 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs181880957 Functional Loss SNV dbSNP153 33..33 33 - - - 17744 RMVar_ID_17744 Human_SNP_ID_326616168 A-to-I Human chr7 + 75956865 75956865 75956865 CTCGTGCCTCAGTCTCCCGAGTGCCTGGGACTACAGGCACATGCTACCACGCCTGGCTAATTTTT CTCGTGCCTCAGTCTCCCGAGTGCCTGGGACTGCAGGCACATGCTACCACGCCTGGCTAATTTTT A G POR Ensembl:ENSG00000127948 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1420618035 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103197,RMVar_hsa_circ_309727,RMVar_hsa_circ_107617,RMVar_hsa_circ_245763,RMVar_hsa_circ_60938,RMVar_hsa_circ_245762 17745 RMVar_ID_17745 Human_SNP_ID_326629701 A-to-I Human chr7 - 75999075 75999075 75999075 GGAGTACAGTAGCACAATCTCGACTCACTGCAAGCTCTGCCTCCCGGGCTCATGCCATTCTTCTG GGAGTACAGTAGCACAATCTCGACTCACTGCAGGCTCTGCCTCCCGGGCTCATGCCATTCTTCTG T C STYXL1 Ensembl:ENSG00000127952 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1554565336 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16220708 Human_Splice_Rec_879282 RMVar_hsa_circ_245781,RMVar_hsa_circ_100654,RMVar_hsa_circ_245782,RMVar_hsa_circ_245783,RMVar_hsa_circ_376920 17746 RMVar_ID_17746 Human_SNP_ID_326629706 A-to-I Human chr7 - 75999091 75999091 75999091 CTCTGTCACCCAGGCTGGAGTACAGTAGCACAATCTCGACTCACTGCAAGCTCTGCCTCCCGGGC CTCTGTCACCCAGGCTGGAGTACAGTAGCACAGTCTCGACTCACTGCAAGCTCTGCCTCCCGGGC T C STYXL1 Ensembl:ENSG00000127952 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1435045572 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_879282 RMVar_hsa_circ_245781,RMVar_hsa_circ_100654,RMVar_hsa_circ_245782,RMVar_hsa_circ_245783,RMVar_hsa_circ_376920 17747 RMVar_ID_17747 Human_SNP_ID_326629707 A-to-I Human chr7 - 75999097 75999097 75999097 GTCTCGCTCTGTCACCCAGGCTGGAGTACAGTAGCACAATCTCGACTCACTGCAAGCTCTGCCTC GTCTCGCTCTGTCACCCAGGCTGGAGTACAGTCGCACAATCTCGACTCACTGCAAGCTCTGCCTC T G STYXL1 Ensembl:ENSG00000127952 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs370576593 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_879282 RMVar_hsa_circ_245781,RMVar_hsa_circ_100654,RMVar_hsa_circ_245782,RMVar_hsa_circ_245783,RMVar_hsa_circ_376920 17748 RMVar_ID_17748 Human_SNP_ID_326630136 A-to-I Human chr7 - 76000079 76000079 76000079 TCAAGCGATTCTCCTGTCTCTGCCTCCCGCGTAGCTGGGATTACAGGTCCGTGTCACCATGCCCG TCAAGCGATTCTCCTGTCTCTGCCTCCCGCGTGGCTGGGATTACAGGTCCGTGTCACCATGCCCG T C STYXL1 Ensembl:ENSG00000127952 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1255155910 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_245781,RMVar_hsa_circ_100654,RMVar_hsa_circ_245782,RMVar_hsa_circ_245783,RMVar_hsa_circ_376920 17749 RMVar_ID_17749 Human_SNP_ID_326633143 A-to-I Human chr7 - 76011032 76011032 76011032 TTTAAAATTTTTTGCAGATACAGGGTCTTGCTATGTTCCCCAGGCTGGTCCAAAACTCCTGACCT TTTAAAATTTTTTGCAGATACAGGGTCTTGCTGTGTTCCCCAGGCTGGTCCAAAACTCCTGACCT T C STYXL1 Ensembl:ENSG00000127952 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs978477675 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5666,RMVar_hsa_circ_245783,RMVar_hsa_circ_307213,RMVar_hsa_circ_245786,RMVar_hsa_circ_117234,RMVar_hsa_circ_245785,RMVar_hsa_circ_303732,RMVar_hsa_circ_349443,RMVar_hsa_circ_290357,RMVar_hsa_circ_245788,RMVar_hsa_circ_245787,RMVar_hsa_circ_245792,RMVar_hsa_circ_303366,RMVar_hsa_circ_362927,RMVar_hsa_circ_63491 17750 RMVar_ID_17750 Human_SNP_ID_326633162 A-to-I Human chr7 - 76011094 76011094 76011094 CTCCAGCCTCAGCCTCTTGAGTAGGTGGGACTACAGATGCATGCCACCACAGTCAGCTAAGTTTT CTCCAGCCTCAGCCTCTTGAGTAGGTGGGACTGCAGATGCATGCCACCACAGTCAGCTAAGTTTT T C STYXL1 Ensembl:ENSG00000127952 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs776301055 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5666,RMVar_hsa_circ_245783,RMVar_hsa_circ_307213,RMVar_hsa_circ_245786,RMVar_hsa_circ_117234,RMVar_hsa_circ_245785,RMVar_hsa_circ_303732,RMVar_hsa_circ_349443,RMVar_hsa_circ_290357,RMVar_hsa_circ_245788,RMVar_hsa_circ_245787,RMVar_hsa_circ_245792,RMVar_hsa_circ_303366,RMVar_hsa_circ_362927,RMVar_hsa_circ_63491 17751 RMVar_ID_17751 Human_SNP_ID_326633494 A-to-I Human chr7 - 76012670 76012670 76012670 ATAAATGGAGCTGGCTGTGGTGGCTCACGCCTATAATCCCAGCACTTTTGGAGGCCAAGCTGGAT ATAAATGGAGCTGGCTGTGGTGGCTCACGCCTGTAATCCCAGCACTTTTGGAGGCCAAGCTGGAT T C STYXL1 Ensembl:ENSG00000127952 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1432474019 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5666,RMVar_hsa_circ_245783,RMVar_hsa_circ_307213,RMVar_hsa_circ_245786,RMVar_hsa_circ_117234,RMVar_hsa_circ_245785,RMVar_hsa_circ_303732,RMVar_hsa_circ_349443,RMVar_hsa_circ_290357,RMVar_hsa_circ_245788,RMVar_hsa_circ_245787,RMVar_hsa_circ_245792,RMVar_hsa_circ_303366,RMVar_hsa_circ_362927,RMVar_hsa_circ_63491 17752 RMVar_ID_17752 Human_SNP_ID_326634870 A-to-I Human chr7 - 76017629 76017629 76017629 CACCCGCCTTGGCCTCCCAAAGTATTGGGATTACAGGTGTGAGCCATCGCGCCTGGCCCCAGTAG CACCCGCCTTGGCCTCCCAAAGTATTGGGATTGCAGGTGTGAGCCATCGCGCCTGGCCCCAGTAG T C STYXL1 Ensembl:ENSG00000127952 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1554574416 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5666,RMVar_hsa_circ_245786,RMVar_hsa_circ_117234,RMVar_hsa_circ_303732,RMVar_hsa_circ_349443,RMVar_hsa_circ_245787,RMVar_hsa_circ_245793,RMVar_hsa_circ_309003,RMVar_hsa_circ_362927,RMVar_hsa_circ_63491,RMVar_hsa_circ_377531,RMVar_hsa_circ_311694,RMVar_hsa_circ_83205,RMVar_hsa_circ_289988,RMVar_hsa_circ_245795,RMVar_hsa_circ_245794 17753 RMVar_ID_17753 Human_SNP_ID_326635413 A-to-I Human chr7 - 76019583 76019583 76019583 GGAAGCAGAGTTAGCCAGGCACGGTGCCTCACACTCGTAATCCCAGCACTTTGTGAGGCTGAGGC GGAAGCAGAGTTAGCCAGGCACGGTGCCTCACGCTCGTAATCCCAGCACTTTGTGAGGCTGAGGC T C STYXL1 Ensembl:ENSG00000127952 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1250006844 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5666,RMVar_hsa_circ_245786,RMVar_hsa_circ_117234,RMVar_hsa_circ_303732,RMVar_hsa_circ_349443,RMVar_hsa_circ_245787,RMVar_hsa_circ_245793,RMVar_hsa_circ_309003,RMVar_hsa_circ_362927,RMVar_hsa_circ_63491,RMVar_hsa_circ_377531,RMVar_hsa_circ_311694,RMVar_hsa_circ_83205,RMVar_hsa_circ_289988,RMVar_hsa_circ_245795,RMVar_hsa_circ_245794 17754 RMVar_ID_17754 Human_SNP_ID_326638880 A-to-I Human chr7 - 76032086 76032086 76032086 TGCCCAGCTAATTTGTATTACAGGGTCTTGCTATGTGGTCCAGGCTGGTCTTGAATTCCTGGGAT TGCCCAGCTAATTTGTATTACAGGGTCTTGCTGTGTGGTCCAGGCTGGTCTTGAATTCCTGGGAT T C STYXL1 Ensembl:ENSG00000127952 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs782386836 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7758154 RMVar_hsa_circ_245793,RMVar_hsa_circ_83205 17755 RMVar_ID_17755 Human_SNP_ID_326639936 A-to-I Human chr7 - 76036382 76036382 76036382 CTAAACTCTCCAGGGACCAGGCGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAG CTAAACTCTCCAGGGACCAGGCGTGGTGGCTCGCGCCTGTAATCCCAGCACTTTGGGAGGCCAAG T C STYXL1 Ensembl:ENSG00000127952 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335856628 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_245793,RMVar_hsa_circ_83205 17756 RMVar_ID_17756 Human_SNP_ID_326640726 A-to-I Human chr7 - 76039349 76039349 76039349 ACCCTTGGCTGGGCGCAGTGGCTCACGCCTGTAATCCCACCACTTTGGGAGGCTGAGGCGGGAAG ACCCTTGGCTGGGCGCAGTGGCTCACGCCTGTCATCCCACCACTTTGGGAGGCTGAGGCGGGAAG T G STYXL1 Ensembl:ENSG00000127952 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs993967210 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_245793,RMVar_hsa_circ_83205 17757 RMVar_ID_17757 Human_SNP_ID_326640829 A-to-I Human chr7 - 76039804 76039804 76039804 CGTCTCTATAAAAATACAAAAATTAGCCTGTCATGGTGGTGCATGCCTGTAGTCCTTGCTACTGG CGTCTCTATAAAAATACAAAAATTAGCCTGTCGTGGTGGTGCATGCCTGTAGTCCTTGCTACTGG T C STYXL1 Ensembl:ENSG00000127952 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs576731139 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10360951 Human_miRNA_ID_2753433,Human_miRNA_ID_2753434,Human_miRNA_ID_2755367,Human_miRNA_ID_2755368 RMVar_hsa_circ_245793,RMVar_hsa_circ_83205 17758 RMVar_ID_17758 Human_SNP_ID_326640830 A-to-I Human chr7 - 76039804 76039804 76039804 CGTCTCTATAAAAATACAAAAATTAGCCTGTCATGGTGGTGCATGCCTGTAGTCCTTGCTACTGG CGTCTCTATAAAAATACAAAAATTAGCCTGTCCTGGTGGTGCATGCCTGTAGTCCTTGCTACTGG T G STYXL1 Ensembl:ENSG00000127952 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs576731139 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10360951 Human_miRNA_ID_2753433,Human_miRNA_ID_2753434,Human_miRNA_ID_2755367,Human_miRNA_ID_2755368 RMVar_hsa_circ_245793,RMVar_hsa_circ_83205 17759 RMVar_ID_17759 Human_SNP_ID_326641008 A-to-I Human chr7 - 76040595 76040595 76040595 TGACTTCACAAACCTCCTGCCTCGGTCTCCCAAAGCGCTGGGATTGCAGGCGTGAGCCACCGTGC TGACTTCACAAACCTCCTGCCTCGGTCTCCCAGAGCGCTGGGATTGCAGGCGTGAGCCACCGTGC T C STYXL1 Ensembl:ENSG00000127952 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1280465634 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_245793,RMVar_hsa_circ_83205 17760 RMVar_ID_17760 Human_SNP_ID_326641018 A-to-I Human chr7 - 76040654 76040654 76040654 TTTTGTATTTTTAGTAGAGACTAGGTTTTACCATGTTGGTCAGGCTGGTCTTGAACTCCTGACTT TTTTGTATTTTTAGTAGAGACTAGGTTTTACCTTGTTGGTCAGGCTGGTCTTGAACTCCTGACTT T A STYXL1 Ensembl:ENSG00000127952 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971383225 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_245793,RMVar_hsa_circ_83205 17761 RMVar_ID_17761 Human_SNP_ID_326641019 A-to-I Human chr7 - 76040654 76040654 76040654 TTTTGTATTTTTAGTAGAGACTAGGTTTTACCATGTTGGTCAGGCTGGTCTTGAACTCCTGACTT TTTTGTATTTTTAGTAGAGACTAGGTTTTACCGTGTTGGTCAGGCTGGTCTTGAACTCCTGACTT T C STYXL1 Ensembl:ENSG00000127952 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971383225 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_245793,RMVar_hsa_circ_83205 17762 RMVar_ID_17762 Human_SNP_ID_326641020 A-to-I Human chr7 - 76040654 76040654 76040654 TTTTGTATTTTTAGTAGAGACTAGGTTTTACCATGTTGGTCAGGCTGGTCTTGAACTCCTGACTT TTTTGTATTTTTAGTAGAGACTAGGTTTTACCCTGTTGGTCAGGCTGGTCTTGAACTCCTGACTT T G STYXL1 Ensembl:ENSG00000127952 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971383225 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_245793,RMVar_hsa_circ_83205 17763 RMVar_ID_17763 Human_SNP_ID_326641038 A-to-I Human chr7 - 76040724 76040724 76040724 TCAAGCGATTTTCCTGCCTCAGCCTCCGGAGTAGCTGGGATTACAGGTATGCGCCACCACGCCTG TCAAGCGATTTTCCTGCCTCAGCCTCCGGAGTGGCTGGGATTACAGGTATGCGCCACCACGCCTG T C STYXL1 Ensembl:ENSG00000127952 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1226158361 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_245793,RMVar_hsa_circ_83205 17764 RMVar_ID_17764 Human_SNP_ID_326641129 A-to-I Human chr7 - 76041102 76041102 76041102 GAATTCCTGGCCTCAAGTGATTCTCCCAGCTCAGCCTCCCAAAGTGCTGGGATTACAAGTGTGAG GAATTCCTGGCCTCAAGTGATTCTCCCAGCTCGGCCTCCCAAAGTGCTGGGATTACAAGTGTGAG T C STYXL1 Ensembl:ENSG00000127952 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1391467430 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_245793,RMVar_hsa_circ_83205 17765 RMVar_ID_17765 Human_SNP_ID_326642039 A-to-I Human chr7 - 76044864 76044864 76044864 TGGCAAAACCCCATCTCTACAAAAAGTACGAAAATTCTCTGGGCGTGATGGTGTGTGCTTGTAGT TGGCAAAACCCCATCTCTACAAAAAGTACGAAGATTCTCTGGGCGTGATGGTGTGTGCTTGTAGT T C AC006330.1,STYXL1 Ensembl:ENSG00000280388,Ensembl:ENSG00000127952 Other,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1358066665 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2046943 RMVar_hsa_circ_245793,RMVar_hsa_circ_83205 17766 RMVar_ID_17766 Human_SNP_ID_326642043 A-to-I Human chr7 - 76044872 76044872 76044872 GGGTAACATGGCAAAACCCCATCTCTACAAAAAGTACGAAAATTCTCTGGGCGTGATGGTGTGTG GGGTAACATGGCAAAACCCCATCTCTACAAAAGGTACGAAAATTCTCTGGGCGTGATGGTGTGTG T C AC006330.1,STYXL1 Ensembl:ENSG00000280388,Ensembl:ENSG00000127952 Other,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1358144693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2046943 RMVar_hsa_circ_245793,RMVar_hsa_circ_83205 17767 RMVar_ID_17767 Human_SNP_ID_326642054 A-to-I Human chr7 - 76044923 76044923 76044923 TGAGCAGCCAAGGCGGACGATCACTTGAGCTCAGGAATTCAGGACCAGCCTGGGTAACATGGCAA TGAGCAGCCAAGGCGGACGATCACTTGAGCTCCGGAATTCAGGACCAGCCTGGGTAACATGGCAA T G AC006330.1,STYXL1 Ensembl:ENSG00000280388,Ensembl:ENSG00000127952 Other,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs918195201 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18104072 RMVar_hsa_circ_245793,RMVar_hsa_circ_83205 17768 RMVar_ID_17768 Human_SNP_ID_326642191 A-to-I Human chr7 - 76045453 76045453 76045453 ACCTCAAGTGATCTGCCCGAGTCAGCCTCTCAAAGTGCTGGGATTATAGGCGTGAGCCACTGCAC ACCTCAAGTGATCTGCCCGAGTCAGCCTCTCAGAGTGCTGGGATTATAGGCGTGAGCCACTGCAC T C AC006330.1,STYXL1 Ensembl:ENSG00000280388,Ensembl:ENSG00000127952 Other,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264632637 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_245793,RMVar_hsa_circ_83205 17769 RMVar_ID_17769 Human_SNP_ID_326642745 A-to-I Human chr7 - 76046782 76046782 76046782 GCCCAGCGTGGTGGTGTACACCTGTAGCCCCAACTACTCCGGAGGCTGAGGCAGGAGAATCGCTT GCCCAGCGTGGTGGTGTACACCTGTAGCCCCAGCTACTCCGGAGGCTGAGGCAGGAGAATCGCTT T C STYXL1 Ensembl:ENSG00000127952 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs550302769 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_245793,RMVar_hsa_circ_83205 17770 RMVar_ID_17770 Human_SNP_ID_326642857 A-to-I Human chr7 - 76047178 76047178 76047178 TGGCTCACTGCAACCTCTGCCTGTCAGGTTCAAGTGGTTCTCCTGCCTCATTCTCCTGAGTAGCT TGGCTCACTGCAACCTCTGCCTGTCAGGTTCAGGTGGTTCTCCTGCCTCATTCTCCTGAGTAGCT T C STYXL1 Ensembl:ENSG00000127952 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs914943952 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8271993 Human_miRNA_ID_2927713,Human_miRNA_ID_2927714 RMVar_hsa_circ_245793,RMVar_hsa_circ_83205 17771 RMVar_ID_17771 Human_SNP_ID_326644387 A-to-I Human chr7 + 76052209 76052209 76052209 CTTTGTTAGATAAAGATAGAGACAGTCTGGGCATGGTAGCTTACACCTATAATCCCAGCACTTGA CTTTGTTAGATAAAGATAGAGACAGTCTGGGCGTGGTAGCTTACACCTATAATCCCAGCACTTGA A G MDH2 Ensembl:ENSG00000146701 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1204492559 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16221222 RMVar_hsa_circ_123878,RMVar_hsa_circ_245800 17772 RMVar_ID_17772 Human_SNP_ID_326710331 A-to-I Human chr7 + 76307046 76307046 76307046 GGTCTCAAATTCTGAAAGAGGAGAATTGCCTGAACCTAGGAGGTGGAGGCTGCAGCGAGCTGAGA GGTCTCAAATTCTGAAAGAGGAGAATTGCCTGTACCTAGGAGGTGGAGGCTGCAGCGAGCTGAGA A T lnc-HSPB1-1 RNACentral:URS00008B41A3 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1338002337 Functional Loss SNV dbSNP153 33..33 33 - - - 17773 RMVar_ID_17773 Human_SNP_ID_326719937 A-to-I Human chr7 - 76339867 76339867 76339867 CCAGCCTGGTCTCGAACTCCTGAGCTCAGGCAATTCACCCGCCTTGGCCTTCCAGAGTGCTGGGA CCAGCCTGGTCTCGAACTCCTGAGCTCAGGCAGTTCACCCGCCTTGGCCTTCCAGAGTGCTGGGA T C YWHAG Ensembl:ENSG00000170027 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1300665216 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100609,RMVar_hsa_circ_245821 17774 RMVar_ID_17774 Human_SNP_ID_326720221 A-to-I Human chr7 - 76340937 76340937 76340937 TTGAGCCCGAGGCTGCAGTGGGCCCTGATCATACTACTGCACTCCAGCCTGGGTGACAGAGTGAG TTGAGCCCGAGGCTGCAGTGGGCCCTGATCATGCTACTGCACTCCAGCCTGGGTGACAGAGTGAG T C YWHAG Ensembl:ENSG00000170027 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1306147831 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10361018,Human_RBP_ID_16221851,Human_RBP_ID_26139141 RMVar_hsa_circ_100609,RMVar_hsa_circ_245821 17775 RMVar_ID_17775 Human_SNP_ID_326721898 A-to-I Human chr7 - 76347534 76347534 76347534 TTTCCCAGGCTGGAGTTCAATGGCACGATCTCAGCTCACTGCAACCTCCACCTCCCAGGTTCAAG TTTCCCAGGCTGGAGTTCAATGGCACGATCTCGGCTCACTGCAACCTCCACCTCCCAGGTTCAAG T C YWHAG Ensembl:ENSG00000170027 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1281968900 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100609,RMVar_hsa_circ_245821,RMVar_hsa_circ_77067,RMVar_hsa_circ_245828 17776 RMVar_ID_17776 Human_SNP_ID_326723541 A-to-I Human chr7 - 76353315 76353315 76353315 CTAGCTACTTGGGAGGCTGAGGCCGGAGAATTACTTGAACCTGGGAGGTGGAGGTTGCAGGGAGT CTAGCTACTTGGGAGGCTGAGGCCGGAGAATTGCTTGAACCTGGGAGGTGGAGGTTGCAGGGAGT T C YWHAG Ensembl:ENSG00000170027 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs566532730 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100609,RMVar_hsa_circ_245821 17777 RMVar_ID_17777 Human_SNP_ID_326723542 A-to-I Human chr7 - 76353315 76353315 76353315 CTAGCTACTTGGGAGGCTGAGGCCGGAGAATTACTTGAACCTGGGAGGTGGAGGTTGCAGGGAGT CTAGCTACTTGGGAGGCTGAGGCCGGAGAATTCCTTGAACCTGGGAGGTGGAGGTTGCAGGGAGT T G YWHAG Ensembl:ENSG00000170027 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs566532730 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100609,RMVar_hsa_circ_245821 17778 RMVar_ID_17778 Human_SNP_ID_326737920 A-to-I Human chr7 + 76405384 76405384 76405384 TTTTTTTTTTGGTAGAGAGGGTGTTTCACCATATTGGCCAGGCTGGTTTCGAACTCCTGACCTTA TTTTTTTTTTGGTAGAGAGGGTGTTTCACCATGTTGGCCAGGCTGGTTTCGAACTCCTGACCTTA A G ZP3 Ensembl:ENSG00000188372 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs556899829 Functional Loss SNV dbSNP153 33..33 33 - - - 17779 RMVar_ID_17779 Human_SNP_ID_326737921 A-to-I Human chr7 + 76405384 76405384 76405384 TTTTTTTTTTGGTAGAGAGGGTGTTTCACCATATTGGCCAGGCTGGTTTCGAACTCCTGACCTTA TTTTTTTTTTGGTAGAGAGGGTGTTTCACCATTTTGGCCAGGCTGGTTTCGAACTCCTGACCTTA A T ZP3 Ensembl:ENSG00000188372 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs556899829 Functional Loss SNV dbSNP153 33..33 33 - - - 17780 RMVar_ID_17780 Human_SNP_ID_326739164 A-to-I Human chr7 + 76410126 76410126 76410126 ACGATTTCGGCTCCCTGCATCCTCCGCCTCCCAGGCTTAATCAATTCTCGTGCCTCAGCGCCCGA ACGATTTCGGCTCCCTGCATCCTCCGCCTCCCGGGCTTAATCAATTCTCGTGCCTCAGCGCCCGA A G ZP3 Ensembl:ENSG00000188372 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs573379379 Functional Loss SNV dbSNP153 33..33 33 - - - 17781 RMVar_ID_17781 Human_SNP_ID_326739473 A-to-I Human chr7 + 76411289 76411289 76411289 TCTCGTCTTTCCCATTAAAGCAAACAGTGGCCAGGAGTAGTGGCTCATGCCTGTAATCCCAACAC TCTCGTCTTTCCCATTAAAGCAAACAGTGGCCGGGAGTAGTGGCTCATGCCTGTAATCCCAACAC A G ZP3 Ensembl:ENSG00000188372 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs954072366 Functional Loss SNV dbSNP153 33..33 33 - - - 17782 RMVar_ID_17782 Human_SNP_ID_326739485 A-to-I Human chr7 + 76411357 76411357 76411357 CGGAAGCAAAGGCAGGAGGATCGCTTGAGACCAAGAGCTCAAGACCAGCCTGGGCAACATAGGGA CGGAAGCAAAGGCAGGAGGATCGCTTGAGACCCAGAGCTCAAGACCAGCCTGGGCAACATAGGGA A C ZP3 Ensembl:ENSG00000188372 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1274092907 Functional Loss SNV dbSNP153 33..33 33 - - - 17783 RMVar_ID_17783 Human_SNP_ID_326741458 A-to-I Human chr7 + 76417660 76417660 76417660 CGAGACAAGATCTCACTCTTGTCTCCCTGGCTAGAGTGCAGTGGTGTGATCATAGTTCATTGCAG CGAGACAAGATCTCACTCTTGTCTCCCTGGCTGGAGTGCAGTGGTGTGATCATAGTTCATTGCAG A G ZP3 Ensembl:ENSG00000188372 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1055851468 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8671561 17784 RMVar_ID_17784 Human_SNP_ID_326760947 A-to-I Human chr7 + 76484035 76484035 76484035 GCTGTGATCGCACCACTGCACTTCAGCCCCCTAGGTGACAGAGCGAGACCCTGTCTTAAAGCTGG GCTGTGATCGCACCACTGCACTTCAGCCCCCTGGGTGACAGAGCGAGACCCTGTCTTAAAGCTGG A G DTX2 Ensembl:ENSG00000091073 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs925825995 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_352406,RMVar_hsa_circ_245844 17785 RMVar_ID_17785 Human_SNP_ID_326761654 A-to-I Human chr7 + 76487308 76487308 76487308 CCAAACTCTTGGCCTCCCAAAGCACTGGGATTACAAGTGTGAGCCACCGTGCCCTGCCTCTTCTT CCAAACTCTTGGCCTCCCAAAGCACTGGGATTGCAAGTGTGAGCCACCGTGCCCTGCCTCTTCTT A G DTX2 Ensembl:ENSG00000091073 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1165411700 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_352406,RMVar_hsa_circ_245844 17786 RMVar_ID_17786 Human_SNP_ID_326761958 A-to-I Human chr7 + 76489340 76489340 76489340 AGGTGTGGTGGTGCTCACTTGTAGTCCCAGCTACTCAGGAGGGTGAGGCAGGAGGATCACTTGAA AGGTGTGGTGGTGCTCACTTGTAGTCCCAGCTGCTCAGGAGGGTGAGGCAGGAGGATCACTTGAA A G DTX2 Ensembl:ENSG00000091073 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1161488250 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_352406,RMVar_hsa_circ_245844 17787 RMVar_ID_17787 Human_SNP_ID_326770088 A-to-I Human chr7 + 76521245 76521245 76521245 AAAATTAGCCAGGCATGGTGATGGGCGCCTGTAATTTCAGCTACTTGGGAGGCTGAGGCAGGAGA AAAATTAGCCAGGCATGGTGATGGGCGCCTGTCATTTCAGCTACTTGGGAGGCTGAGGCAGGAGA A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs555200172 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86873,RMVar_hsa_circ_245848 17788 RMVar_ID_17788 Human_SNP_ID_326774973 A-to-I Human chr7 + 76546564 76546563 76546564 TTACTTGGGAGGCTGAGGCAGGAGAATCGCTTAAACTGGGGAGGCAGAGGTTGCAGTGAGCCGAG TTACTTGGGAGGCTGAGGCAGGAGAATCGCTT_AACTGGGGAGGCAGAGGTTGCAGTGAGCCGAG TA T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1197269906 Functional Loss DEL dbSNP153 33..33 33 - - - 17789 RMVar_ID_17789 Human_SNP_ID_326787316 A-to-I Human chr7 + 76602328 76602328 76602328 AATTTAACTCAAATTAAAACCCCATCTCTACTAAAAATACAAAAAATTAGCTGGGCGTGGTGGCA AATTTAACTCAAATTAAAACCCCATCTCTACTGAAAATACAAAAAATTAGCTGGGCGTGGTGGCA A G AC004980.1 Ensembl:ENSG00000205485 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1405985433 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17428663,Human_RBP_ID_18520289 17790 RMVar_ID_17790 Human_SNP_ID_326788845 A-to-I Human chr7 + 76607679 76607679 76607679 TTTTGAGAGGGTCTTGCTCTGTCACTCTGGCTAGAGCGCAGCAGGAGGCAGCAAGGCTGGGACCT TTTTGAGAGGGTCTTGCTCTGTCACTCTGGCTGGAGCGCAGCAGGAGGCAGCAAGGCTGGGACCT A G AC004980.1 Ensembl:ENSG00000205485 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1024703625 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16223283 17791 RMVar_ID_17791 Human_SNP_ID_326790696 A-to-I Human chr7 + 76613638 76613635 76613638 AGCCTCCCAAGTAGATGGGATTATGGGTACCCACCACCACACCAGGCTAGTTTTTGTATTTGTAG AGCCTCCCAAGTAGATGGGATTATGGGTAC___CCACCACACCAGGCTAGTTTTTGTATTTGTAG CCCA C AC004980.1 Ensembl:ENSG00000205485 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1380220792 Functional Loss DEL dbSNP153 31..33 33 - - - 17792 RMVar_ID_17792 Human_SNP_ID_326791821 A-to-I Human chr7 + 76618495 76618495 76618495 AATACAAAAATTAGCTGGGTGCAGCAGTGCACACCTGTAATCCACCTACTCGGGAGGCTGAGGCA AATACAAAAATTAGCTGGGTGCAGCAGTGCACCCCTGTAATCCACCTACTCGGGAGGCTGAGGCA A C AC004980.1 Ensembl:ENSG00000205485 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs764281912 Functional Loss SNV dbSNP153 33..33 33 - - - 17793 RMVar_ID_17793 Human_SNP_ID_326791828 A-to-I Human chr7 + 76618501 76618501 76618501 AAAATTAGCTGGGTGCAGCAGTGCACACCTGTAATCCACCTACTCGGGAGGCTGAGGCAGGAGAA AAAATTAGCTGGGTGCAGCAGTGCACACCTGTCATCCACCTACTCGGGAGGCTGAGGCAGGAGAA A C AC004980.1 Ensembl:ENSG00000205485 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs780025365 Functional Loss SNV dbSNP153 33..33 33 - - - 17794 RMVar_ID_17794 Human_SNP_ID_326792592 A-to-I Human chr7 + 76620633 76620633 76620633 GAGACTACAGGCGTGTCCCACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTACG GAGACTACAGGCGTGTCCCACCATGCCTGGCTGATTTTTGTATTTTTAGTAGAGATGGGGTTACG A G AC004980.1 Ensembl:ENSG00000205485 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1424807531 Functional Loss SNV dbSNP153 33..33 33 - - - 17795 RMVar_ID_17795 Human_SNP_ID_326793031 A-to-I Human chr7 + 76621819 76621819 76621819 AAAAGTAGCCGGATATGGTGGCGGGCACCTGCAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAAGTAGCCGGATATGGTGGCGGGCACCTGCGGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA A G AC004980.1 Ensembl:ENSG00000205485 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1183063394 Functional Loss SNV dbSNP153 33..33 33 - - - 17796 RMVar_ID_17796 Human_SNP_ID_326869765 A-to-I Human chr7 + 76979990 76979990 76979990 CGTGTTTGTTTGTTTGTTTGTTTGTTTTTTGTAAAGACTGGGTCTCCATCGCCCTGTGTTGCCCA CGTGTTTGTTTGTTTGTTTGTTTGTTTTTTGTGAAGACTGGGTCTCCATCGCCCTGTGTTGCCCA A G DTX2P1-UPK3BP1-PMS2P11,DTX2P1 Ensembl:ENSG00000265479,Ensembl:ENSG00000186704 lincRNA,Pseudogene intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs887834060 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124405,RMVar_hsa_circ_245858 17797 RMVar_ID_17797 Human_SNP_ID_326871070 A-to-I Human chr7 + 76985410 76985410 76985410 CCAAACTCTTGGCCTCCCAAAGCACTGGGATTACAAGTGTGAGCCACCGTGCCCTGCCTCTTCTT CCAAACTCTTGGCCTCCCAAAGCACTGGGATTGCAAGTGTGAGCCACCGTGCCCTGCCTCTTCTT A G DTX2P1-UPK3BP1-PMS2P11,DTX2P1 Ensembl:ENSG00000265479,Ensembl:ENSG00000186704 lincRNA,Pseudogene intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs938661426 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124405,RMVar_hsa_circ_245858 17798 RMVar_ID_17798 Human_SNP_ID_326871071 A-to-I Human chr7 + 76985410 76985410 76985410 CCAAACTCTTGGCCTCCCAAAGCACTGGGATTACAAGTGTGAGCCACCGTGCCCTGCCTCTTCTT CCAAACTCTTGGCCTCCCAAAGCACTGGGATTTCAAGTGTGAGCCACCGTGCCCTGCCTCTTCTT A T DTX2P1-UPK3BP1-PMS2P11,DTX2P1 Ensembl:ENSG00000265479,Ensembl:ENSG00000186704 lincRNA,Pseudogene intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs938661426 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124405,RMVar_hsa_circ_245858 17799 RMVar_ID_17799 Human_SNP_ID_326878826 A-to-I Human chr7 + 77007911 77007911 77007911 CAGGATTGCCATGGCTTTTTTGTTTTTTTTTTAACGTGGAGTCTCACTCTGTTGCCCAGGCTGGA CAGGATTGCCATGGCTTTTTTGTTTTTTTTTTGACGTGGAGTCTCACTCTGTTGCCCAGGCTGGA A G DTX2P1-UPK3BP1-PMS2P11 Ensembl:ENSG00000265479 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1172694086 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16068,RMVar_hsa_circ_265160 17800 RMVar_ID_17800 Human_SNP_ID_326878832 A-to-I Human chr7 + 77007924 77007920 77007924 GCTTTTTTGTTTTTTTTTTAACGTGGAGTCTCACTCTGTTGCCCAGGCTGGAGTGCTGTGGCGCG GCTTTTTTGTTTTTTTTTTAACGTGGAGT____CTCTGTTGCCCAGGCTGGAGTGCTGTGGCGCG TCTCA T DTX2P1-UPK3BP1-PMS2P11 Ensembl:ENSG00000265479 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1259367794 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_16068,RMVar_hsa_circ_265160 17801 RMVar_ID_17801 Human_SNP_ID_326880145 A-to-I Human chr7 + 77011184 77011184 77011184 AAAATTAGCCAGGCATGGTGATGGGCGCCTGTAATTTCAGCTACTTGGGAGGCTGAGGCAGGAGA AAAATTAGCCAGGCATGGTGATGGGCGCCTGTCATTTCAGCTACTTGGGAGGCTGAGGCAGGAGA A C DTX2P1-UPK3BP1-PMS2P11 Ensembl:ENSG00000265479 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs183987296 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16068,RMVar_hsa_circ_265160 17802 RMVar_ID_17802 Human_SNP_ID_326887878 A-to-I Human chr7 + 77049951 77049951 77049951 AAAGTTGGTCGGACGTACAGACGGGTGCCTGTAGTCCCAGCTGCTTGGGAGACTGAGGCAGGAGA AAAGTTGGTCGGACGTACAGACGGGTGCCTGTGGTCCCAGCTGCTTGGGAGACTGAGGCAGGAGA A G AC007000.4 Ensembl:ENSG00000259628 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1237908722 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7758828 17803 RMVar_ID_17803 Human_SNP_ID_327000911 A-to-I Human chr7 - 77520934 77520934 77520934 AAAATTAAATGGGCGTGGTGGTGCGTGCCTGTAGTCCCAGCTACTCGGGGAGGCTGAGGCAGGAG AAAATTAAATGGGCGTGGTGGTGCGTGCCTGTTGTCCCAGCTACTCGGGGAGGCTGAGGCAGGAG T A lnc-GSAP-5,APTR,lnc-GSAP-1,lnc-GSAP-1:2 RNACentral:URS0000D5A3A5,RNACentral:URS0000D5A265,RNACentral:URS00008BD74F,RNACentral:URS00008BBC27 lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1330848482 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_245895 17804 RMVar_ID_17804 Human_SNP_ID_327001693 A-to-I Human chr7 - 77524184 77524184 77524184 ATTGTTGTGCAACAGATCTCCAGAAACTTTTCATCTTGCAAAACTGAATATGTATACTCATTAAA ATTGTTGTGCAACAGATCTCCAGAAACTTTTCGTCTTGCAAAACTGAATATGTATACTCATTAAA T C lnc-GSAP-5,APTR,lnc-GSAP-1 RNACentral:URS0000D5A3A5,RNACentral:URS0000D5A265,RNACentral:URS00008BD74F lincRNA,lincRNA,lincRNA intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1373690183 Functional Loss SNV dbSNP153 33..33 33 - - - 17805 RMVar_ID_17805 Human_SNP_ID_327011267 A-to-I Human chr7 + 77556324 77556324 77556324 GGCTGAAGAGACCTGCCTACCTCTGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCCAGA GGCTGAAGAGACCTGCCTACCTCTGCCTCCCAGAGTGCTGGGATTACAGGCATGAGCCACCCAGA A G PTPN12 Ensembl:ENSG00000127947 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1250341999 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126270,RMVar_hsa_circ_245896 17806 RMVar_ID_17806 Human_SNP_ID_327016052 A-to-I Human chr7 + 77573941 77573941 77573941 CGCTGCCACATCCGGCTAATTTTTGTATTGTTAGTAGAGACGTGGTTTCACCATGTTGGCCAGGC CGCTGCCACATCCGGCTAATTTTTGTATTGTTGGTAGAGACGTGGTTTCACCATGTTGGCCAGGC A G PTPN12 Ensembl:ENSG00000127947 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1045669337 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26400,RMVar_hsa_circ_126270,RMVar_hsa_circ_279466,RMVar_hsa_circ_289469,RMVar_hsa_circ_313171,RMVar_hsa_circ_354958,RMVar_hsa_circ_245896,RMVar_hsa_circ_352756,RMVar_hsa_circ_296841,RMVar_hsa_circ_282336,RMVar_hsa_circ_277141,RMVar_hsa_circ_277180,RMVar_hsa_circ_61145,RMVar_hsa_circ_245899,RMVar_hsa_circ_245901,RMVar_hsa_circ_245902,RMVar_hsa_circ_245903,RMVar_hsa_circ_245900,RMVar_hsa_circ_245897,RMVar_hsa_circ_245898 17807 RMVar_ID_17807 Human_SNP_ID_327028670 A-to-I Human chr7 + 77622090 77622090 77622090 GAACCTCCCACCCTAGACTCCCAACTAGCTGGAACTATAGACACACACCACCATGCCTGGCTAAT GAACCTCCCACCCTAGACTCCCAACTAGCTGGCACTATAGACACACACCACCATGCCTGGCTAAT A C PTPN12 Ensembl:ENSG00000127947 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992820561 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73046,RMVar_hsa_circ_26400,RMVar_hsa_circ_282336,RMVar_hsa_circ_61145,RMVar_hsa_circ_245914,RMVar_hsa_circ_79297,RMVar_hsa_circ_355738,RMVar_hsa_circ_347225,RMVar_hsa_circ_75322,RMVar_hsa_circ_91303,RMVar_hsa_circ_113350,RMVar_hsa_circ_245924,RMVar_hsa_circ_276391,RMVar_hsa_circ_289186,RMVar_hsa_circ_270909,RMVar_hsa_circ_245927,RMVar_hsa_circ_245929,RMVar_hsa_circ_245930,RMVar_hsa_circ_245928,RMVar_hsa_circ_245926,RMVar_hsa_circ_300798,RMVar_hsa_circ_245934,RMVar_hsa_circ_61962,RMVar_hsa_circ_245933,RMVar_hsa_circ_64943,RMVar_hsa_circ_309648,RMVar_hsa_circ_290954,RMVar_hsa_circ_245935,RMVar_hsa_circ_245936 17808 RMVar_ID_17808 Human_SNP_ID_327033513 A-to-I Human chr7 + 77638238 77638238 77638238 CCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCGCCTGGCCTGACCTTGTTGAT CCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCCTGGCCTGACCTTGTTGAT A G PTPN12 Ensembl:ENSG00000127947 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs901630208 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113350,RMVar_hsa_circ_245927,RMVar_hsa_circ_245926,RMVar_hsa_circ_12088,RMVar_hsa_circ_245942,RMVar_hsa_circ_245943 17809 RMVar_ID_17809 Human_SNP_ID_327039023 A-to-I Human chr7 - 77658705 77658705 77658705 CTCCTGTCCCGGCACCCCGAAGTGTTGGGACTACAGGCATGAGCCACTGTGCACAGCCCTTTTTG CTCCTGTCCCGGCACCCCGAAGTGTTGGGACTGCAGGCATGAGCCACTGTGCACAGCCCTTTTTG T C APTR Ensembl:ENSG00000214293 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027404623 Functional Loss SNV dbSNP153 33..33 33 - - - 17810 RMVar_ID_17810 Human_SNP_ID_327043157 A-to-I Human chr7 - 77675159 77675159 77675159 TTGCCAAGGCTGAAGTGCAGTAGTATGATCATAGCTCACTGCAGTCTCAACCTCCTGGCAGTCCT TTGCCAAGGCTGAAGTGCAGTAGTATGATCATGGCTCACTGCAGTCTCAACCTCCTGGCAGTCCT T C APTR Ensembl:ENSG00000214293 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs970258655 Functional Loss SNV dbSNP153 33..33 33 - - - 17811 RMVar_ID_17811 Human_SNP_ID_327050054 A-to-I Human chr7 + 77701035 77701035 77701035 AAAAAATTAGCCGGGTGTGGCGGCACGCACCTATAGTCTCAGCTACCTGGGAGGCTGAGGCATCG AAAAAATTAGCCGGGTGTGGCGGCACGCACCTGTAGTCTCAGCTACCTGGGAGGCTGAGGCATCG A G RSBN1L Ensembl:ENSG00000187257 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1450654801 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87284,RMVar_hsa_circ_106809,RMVar_hsa_circ_245946,RMVar_hsa_circ_245947 17812 RMVar_ID_17812 Human_SNP_ID_327050055 A-to-I Human chr7 + 77701037 77701037 77701037 AAAATTAGCCGGGTGTGGCGGCACGCACCTATAGTCTCAGCTACCTGGGAGGCTGAGGCATCGCT AAAATTAGCCGGGTGTGGCGGCACGCACCTATGGTCTCAGCTACCTGGGAGGCTGAGGCATCGCT A G RSBN1L Ensembl:ENSG00000187257 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1186397813 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87284,RMVar_hsa_circ_106809,RMVar_hsa_circ_245946,RMVar_hsa_circ_245947 17813 RMVar_ID_17813 Human_SNP_ID_327051156 A-to-I Human chr7 + 77704861 77704861 77704861 ATTAGGTGTGTCGGGCGCCTGTTATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCACTTGAA ATTAGGTGTGTCGGGCGCCTGTTATCCCAGCTGCTTGGGAGGCTGAGGCAGGAGAATCACTTGAA A G RSBN1L Ensembl:ENSG00000187257 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1012087598 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87284,RMVar_hsa_circ_106809,RMVar_hsa_circ_245946,RMVar_hsa_circ_245947 17814 RMVar_ID_17814 Human_SNP_ID_327051566 A-to-I Human chr7 + 77706258 77706258 77706258 GCCACTACGTTGGGCTAATTTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGTCCAGGC GCCACTACGTTGGGCTAATTTTTTGTATTTTTGGTAGAGATGGGGTTTCACCATGTTGTCCAGGC A G RSBN1L Ensembl:ENSG00000187257 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348476713 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87284,RMVar_hsa_circ_106809,RMVar_hsa_circ_245946,RMVar_hsa_circ_245947 17815 RMVar_ID_17815 Human_SNP_ID_327054139 A-to-I Human chr7 + 77715492 77715492 77715492 ACACTCGGGTAATTTTTTAAAAATTTTTAGTCAAGATGGGGGGCTCACCATGTTGGCCAGGAAGG ACACTCGGGTAATTTTTTAAAAATTTTTAGTCGAGATGGGGGGCTCACCATGTTGGCCAGGAAGG A G RSBN1L Ensembl:ENSG00000187257 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs901004737 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16225505 RMVar_hsa_circ_87284,RMVar_hsa_circ_106809,RMVar_hsa_circ_245946,RMVar_hsa_circ_245947 17816 RMVar_ID_17816 Human_SNP_ID_327054178 A-to-I Human chr7 + 77715577 77715577 77715577 GTGATTCGCCTGCCGTAGCCTCTCAAAGTGCTAGAATTACAGGCACGACACTGTGCCTGGCCCTA GTGATTCGCCTGCCGTAGCCTCTCAAAGTGCTGGAATTACAGGCACGACACTGTGCCTGGCCCTA A G RSBN1L Ensembl:ENSG00000187257 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1419326358 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87284,RMVar_hsa_circ_106809,RMVar_hsa_circ_245946,RMVar_hsa_circ_245947 17817 RMVar_ID_17817 Human_SNP_ID_327060839 A-to-I Human chr7 + 77739853 77739853 77739853 CTCACTGCAAACTCTGCCTCCTGGGTTCAAGCAGTTTTCCTGCCCCAGCCTCCTGAGTAGCTGGG CTCACTGCAAACTCTGCCTCCTGGGTTCAAGCCGTTTTCCTGCCCCAGCCTCCTGAGTAGCTGGG A C RSBN1L Ensembl:ENSG00000187257 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1305184994 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86223,RMVar_hsa_circ_87284,RMVar_hsa_circ_106809,RMVar_hsa_circ_245946,RMVar_hsa_circ_245947,RMVar_hsa_circ_356272,RMVar_hsa_circ_307448,RMVar_hsa_circ_245948,RMVar_hsa_circ_245949 17818 RMVar_ID_17818 Human_SNP_ID_327061270 A-to-I Human chr7 + 77741267 77741267 77741267 CCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGCACCTGGCCACCATTTTACTTC CCTCAGCCTCCCAAAGTGCTGGGATTACAGGCTTGAGCCACTGCACCTGGCCACCATTTTACTTC A T RSBN1L Ensembl:ENSG00000187257 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs373893593 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86223,RMVar_hsa_circ_87284,RMVar_hsa_circ_106809,RMVar_hsa_circ_245946,RMVar_hsa_circ_245947,RMVar_hsa_circ_356272,RMVar_hsa_circ_307448,RMVar_hsa_circ_245948,RMVar_hsa_circ_245949 17819 RMVar_ID_17819 Human_SNP_ID_327061293 A-to-I Human chr7 + 77741345 77741345 77741345 TTGAAGGGGCAGATTAGTTGGATAGCAGTTCTATTCTTTCTGTTATAGGTACCTGTCAGGATCCT TTGAAGGGGCAGATTAGTTGGATAGCAGTTCTGTTCTTTCTGTTATAGGTACCTGTCAGGATCCT A G RSBN1L Ensembl:ENSG00000187257 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10441228 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_1588,GWAS_ID_1589,GWAS_ID_1590,GWAS_ID_1591,GWAS_ID_1592,GWAS_ID_1593,GWAS_ID_1594,GWAS_ID_1595,GWAS_ID_1596,GWAS_ID_1597,GWAS_ID_1598 RMVar_hsa_circ_86223,RMVar_hsa_circ_87284,RMVar_hsa_circ_106809,RMVar_hsa_circ_245946,RMVar_hsa_circ_245947,RMVar_hsa_circ_356272,RMVar_hsa_circ_307448,RMVar_hsa_circ_245948,RMVar_hsa_circ_245949 17820 RMVar_ID_17820 Human_SNP_ID_327061380 A-to-I Human chr7 + 77741679 77741679 77741679 GTGCCACTGCACTCCAACCTGAGTGACAGAGCAAGACTCGGTCTCAAAAAAAAAAAAAAAGAAAA GTGCCACTGCACTCCAACCTGAGTGACAGAGCGAGACTCGGTCTCAAAAAAAAAAAAAAAGAAAA A G RSBN1L Ensembl:ENSG00000187257 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs964108577 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86223,RMVar_hsa_circ_87284,RMVar_hsa_circ_106809,RMVar_hsa_circ_245946,RMVar_hsa_circ_245947,RMVar_hsa_circ_356272,RMVar_hsa_circ_307448,RMVar_hsa_circ_245948,RMVar_hsa_circ_245949 17821 RMVar_ID_17821 Human_SNP_ID_327062534 A-to-I Human chr7 + 77745487 77745487 77745487 ATTTGTTTCACTCATAGTGTTGATTGACATATAGTATACAGGTATCCTATGAGAGAAACATGTAA ATTTGTTTCACTCATAGTGTTGATTGACATATGGTATACAGGTATCCTATGAGAGAAACATGTAA A G RSBN1L Ensembl:ENSG00000187257 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6976144 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_1599,GWAS_ID_1600,GWAS_ID_1601,GWAS_ID_1602,GWAS_ID_1603,GWAS_ID_1604,GWAS_ID_1605,GWAS_ID_1606,GWAS_ID_1607,GWAS_ID_1608,GWAS_ID_1609,GWAS_ID_1610 RMVar_hsa_circ_86223,RMVar_hsa_circ_87284,RMVar_hsa_circ_106809,RMVar_hsa_circ_245946,RMVar_hsa_circ_245947,RMVar_hsa_circ_356272,RMVar_hsa_circ_307448,RMVar_hsa_circ_245948,RMVar_hsa_circ_245949 17822 RMVar_ID_17822 Human_SNP_ID_327062535 A-to-I Human chr7 + 77745487 77745487 77745487 ATTTGTTTCACTCATAGTGTTGATTGACATATAGTATACAGGTATCCTATGAGAGAAACATGTAA ATTTGTTTCACTCATAGTGTTGATTGACATATTGTATACAGGTATCCTATGAGAGAAACATGTAA A T RSBN1L Ensembl:ENSG00000187257 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6976144 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_1599,GWAS_ID_1600,GWAS_ID_1601,GWAS_ID_1602,GWAS_ID_1603,GWAS_ID_1604,GWAS_ID_1605,GWAS_ID_1606,GWAS_ID_1607,GWAS_ID_1608,GWAS_ID_1609,GWAS_ID_1610 RMVar_hsa_circ_86223,RMVar_hsa_circ_87284,RMVar_hsa_circ_106809,RMVar_hsa_circ_245946,RMVar_hsa_circ_245947,RMVar_hsa_circ_356272,RMVar_hsa_circ_307448,RMVar_hsa_circ_245948,RMVar_hsa_circ_245949 17823 RMVar_ID_17823 Human_SNP_ID_327063321 A-to-I Human chr7 + 77748588 77748588 77748588 TGGCTCACTGCAATCTGCCTCTCAGTTCAAGCAATTCTCCTGCCTCAGCCTCCCGGGTAGCTGGG TGGCTCACTGCAATCTGCCTCTCAGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGGGTAGCTGGG A G RSBN1L Ensembl:ENSG00000187257 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs565371700 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86223,RMVar_hsa_circ_87284,RMVar_hsa_circ_106809,RMVar_hsa_circ_245946,RMVar_hsa_circ_245947,RMVar_hsa_circ_356272,RMVar_hsa_circ_307448,RMVar_hsa_circ_245948,RMVar_hsa_circ_245949 17824 RMVar_ID_17824 Human_SNP_ID_327065309 A-to-I Human chr7 + 77756201 77756201 77756201 TCATCCAGGCTGGAGTGTAGTGGCATGATCTCAGTTCACTGAAACCTCTGTCTCCCGGGTTCAAG TCATCCAGGCTGGAGTGTAGTGGCATGATCTCGGTTCACTGAAACCTCTGTCTCCCGGGTTCAAG A G RSBN1L Ensembl:ENSG00000187257 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1423080249 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9147,RMVar_hsa_circ_86223,RMVar_hsa_circ_87284,RMVar_hsa_circ_106809,RMVar_hsa_circ_245946,RMVar_hsa_circ_245947,RMVar_hsa_circ_356272,RMVar_hsa_circ_245948,RMVar_hsa_circ_245949,RMVar_hsa_circ_306813,RMVar_hsa_circ_359014,RMVar_hsa_circ_302237,RMVar_hsa_circ_122827,RMVar_hsa_circ_245952,RMVar_hsa_circ_245953,RMVar_hsa_circ_245954,RMVar_hsa_circ_245951 17825 RMVar_ID_17825 Human_SNP_ID_327069006 A-to-I Human chr7 + 77770636 77770636 77770636 CCAGGAGTTTGAGGCTGCAGTAAGCTATGAGTACATCACTGCACTCCAGCCTGGGTGACAGAACC CCAGGAGTTTGAGGCTGCAGTAAGCTATGAGTTCATCACTGCACTCCAGCCTGGGTGACAGAACC A T RSBN1L Ensembl:ENSG00000187257 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1012147556 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10361585,Human_RBP_ID_26118613 RMVar_hsa_circ_245955,RMVar_hsa_circ_86223,RMVar_hsa_circ_106809,RMVar_hsa_circ_245947,RMVar_hsa_circ_245949,RMVar_hsa_circ_359014,RMVar_hsa_circ_302237,RMVar_hsa_circ_245953,RMVar_hsa_circ_245954,RMVar_hsa_circ_265948,RMVar_hsa_circ_293608,RMVar_hsa_circ_314560,RMVar_hsa_circ_245957,RMVar_hsa_circ_245958,RMVar_hsa_circ_245956,RMVar_hsa_circ_319876,RMVar_hsa_circ_376757 17826 RMVar_ID_17826 Human_SNP_ID_327070137 A-to-I Human chr7 + 77775182 77775182 77775182 CTCTGTTGCCCAGGCTGGGAGCTCAAAGTGCTAGGATTACAGGTGCGAAACACTGCACCTGGCCT CTCTGTTGCCCAGGCTGGGAGCTCAAAGTGCTGGGATTACAGGTGCGAAACACTGCACCTGGCCT A G RSBN1L Ensembl:ENSG00000187257 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1157726542 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_245955,RMVar_hsa_circ_86223,RMVar_hsa_circ_245949,RMVar_hsa_circ_302237,RMVar_hsa_circ_245954,RMVar_hsa_circ_265948,RMVar_hsa_circ_314560,RMVar_hsa_circ_245957,RMVar_hsa_circ_245956,RMVar_hsa_circ_245961,RMVar_hsa_circ_268970,RMVar_hsa_circ_376757,RMVar_hsa_circ_122039 17827 RMVar_ID_17827 Human_SNP_ID_327071308 A-to-I Human chr7 + 77779461 77779457 77779461 AGAGCTGACATTAACATATATATATATATATAAATATATATATATATTTTGTAATATGAGCCAGA AGAGCTGACATTAACATATATATATATAT____ATATATATATATATTTTGTAATATGAGCCAGA TATAA T RSBN1L Ensembl:ENSG00000187257 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1290505241 Functional Loss DEL dbSNP153 30..33 33 - - - Human_miRNA_ID_155175 RMVar_hsa_circ_245955,RMVar_hsa_circ_265948,RMVar_hsa_circ_268970,RMVar_hsa_circ_266006 17828 RMVar_ID_17828 Human_SNP_ID_327071308 A-to-I Human chr7 + 77779460 77779457 77779461 TAGAGCTGACATTAACATATATATATATATATAAATATATATATATATTTTGTAATATGAGCCAG TAGAGCTGACATTAACATATATATATATAT____ATATATATATATATTTTGTAATATGAGCCAG TATAA T RSBN1L Ensembl:ENSG00000187257 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1290505241 Functional Loss DEL dbSNP153 31..34 33 - - - Human_miRNA_ID_155175 RMVar_hsa_circ_245955,RMVar_hsa_circ_265948,RMVar_hsa_circ_268970,RMVar_hsa_circ_266006 17829 RMVar_ID_17829 Human_SNP_ID_327071309 A-to-I Human chr7 + 77779460 77779457 77779460 TAGAGCTGACATTAACATATATATATATATATAAATATATATATATATTTTGTAATATGAGCCAG TAGAGCTGACATTAACATATATATATATAT___AATATATATATATATTTTGTAATATGAGCCAG TATA T RSBN1L Ensembl:ENSG00000187257 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1321649245 Functional Loss DEL dbSNP153 31..33 33 - - - Human_miRNA_ID_155175 RMVar_hsa_circ_245955,RMVar_hsa_circ_265948,RMVar_hsa_circ_268970,RMVar_hsa_circ_266006 17830 RMVar_ID_17830 Human_SNP_ID_327071316 A-to-I Human chr7 + 77779461 77779461 77779461 AGAGCTGACATTAACATATATATATATATATAAATATATATATATATTTTGTAATATGAGCCAGA AGAGCTGACATTAACATATATATATATATATATATATATATATATATTTTGTAATATGAGCCAGA A T RSBN1L Ensembl:ENSG00000187257 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs4729744 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_155175 RMVar_hsa_circ_245955,RMVar_hsa_circ_265948,RMVar_hsa_circ_268970,RMVar_hsa_circ_266006 17831 RMVar_ID_17831 Human_SNP_ID_327071894 A-to-I Human chr7 + 77781631 77781631 77781631 ATCTAAAAACCATAGTGGTTGCTTTTAGGTATAGTTTCCTATATAACCTATAGTCAGACTTATCT ATCTAAAAACCATAGTGGTTGCTTTTAGGTATGGTTTCCTATATAACCTATAGTCAGACTTATCT A G RSBN1L Ensembl:ENSG00000187257 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1198837987 Functional Loss SNV dbSNP153 33..33 33 - - - 17832 RMVar_ID_17832 Human_SNP_ID_327071919 A-to-I Human chr7 + 77781742 77781742 77781742 TGCAGTGGCTCACGCCTGTAATCCCAGCACTTAGGGAGGCCGAGGCGGGCGGATCACGAGGTCAG TGCAGTGGCTCACGCCTGTAATCCCAGCACTTGGGGAGGCCGAGGCGGGCGGATCACGAGGTCAG A G RSBN1L Ensembl:ENSG00000187257 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs945457534 Functional Loss SNV dbSNP153 33..33 33 - - - 17833 RMVar_ID_17833 Human_SNP_ID_327071920 A-to-I Human chr7 + 77781742 77781742 77781742 TGCAGTGGCTCACGCCTGTAATCCCAGCACTTAGGGAGGCCGAGGCGGGCGGATCACGAGGTCAG TGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGGATCACGAGGTCAG A T RSBN1L Ensembl:ENSG00000187257 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs945457534 Functional Loss SNV dbSNP153 33..33 33 - - - 17834 RMVar_ID_17834 Human_SNP_ID_327072704 A-to-I Human chr7 + 77784467 77784467 77784467 AAAATCGGACGGGCGTGGTGACACGCACCTGTAATCGCAGCTACTGGAGAGGCTGAGGCAGGAGA AAAATCGGACGGGCGTGGTGACACGCACCTGTGATCGCAGCTACTGGAGAGGCTGAGGCAGGAGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1188140804 Functional Loss SNV dbSNP153 33..33 33 - - - 17835 RMVar_ID_17835 Human_SNP_ID_327075324 A-to-I Human chr7 - 77795005 77795005 77795005 GACTACAAGGTGCATACCACCACGCCTTGCCAATTTTTTTATTTTTTGTAGAGGCAGGGTTTCAC GACTACAAGGTGCATACCACCACGCCTTGCCAGTTTTTTTATTTTTTGTAGAGGCAGGGTTTCAC T C TMEM60 Ensembl:ENSG00000135211 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs902485090 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128042,RMVar_hsa_circ_245964 17836 RMVar_ID_17836 Human_SNP_ID_327075325 A-to-I Human chr7 - 77795005 77795005 77795005 GACTACAAGGTGCATACCACCACGCCTTGCCAATTTTTTTATTTTTTGTAGAGGCAGGGTTTCAC GACTACAAGGTGCATACCACCACGCCTTGCCACTTTTTTTATTTTTTGTAGAGGCAGGGTTTCAC T G TMEM60 Ensembl:ENSG00000135211 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs902485090 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128042,RMVar_hsa_circ_245964 17837 RMVar_ID_17837 Human_SNP_ID_327075561 A-to-I Human chr7 - 77796040 77796040 77796040 CCAGCTACTTGGGAAACTTAAGTGGGAGGATCACTTGAACCCGAGAGGCAGAGGCTGCAGTGACC CCAGCTACTTGGGAAACTTAAGTGGGAGGATCCCTTGAACCCGAGAGGCAGAGGCTGCAGTGACC T G TMEM60 Ensembl:ENSG00000135211 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042728918 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128042,RMVar_hsa_circ_245964 17838 RMVar_ID_17838 Human_SNP_ID_327107035 A-to-I Human chr7 + 77930234 77930234 77930234 CCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATAAGCCACCCTGCCCAGTCGGACTAGCCACAT CCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTAAGCCACCCTGCCCAGTCGGACTAGCCACAT A G PHTF2 Ensembl:ENSG00000006576 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886411908 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5513695 RMVar_hsa_circ_100388,RMVar_hsa_circ_245966,RMVar_hsa_circ_37844,RMVar_hsa_circ_47735,RMVar_hsa_circ_302707,RMVar_hsa_circ_245982,RMVar_hsa_circ_245978,RMVar_hsa_circ_342329,RMVar_hsa_circ_293654,RMVar_hsa_circ_47970,RMVar_hsa_circ_245981,RMVar_hsa_circ_356350,RMVar_hsa_circ_245983,RMVar_hsa_circ_245984,RMVar_hsa_circ_245985 17839 RMVar_ID_17839 Human_SNP_ID_327110520 A-to-I Human chr7 + 77943401 77943401 77943401 TGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACAGCGCCCGACCTATTCTT TGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTGCAGGCGTGAGCCACAGCGCCCGACCTATTCTT A G PHTF2 Ensembl:ENSG00000006576 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs943939798 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37844,RMVar_hsa_circ_245982,RMVar_hsa_circ_245978,RMVar_hsa_circ_293654,RMVar_hsa_circ_356350,RMVar_hsa_circ_40818,RMVar_hsa_circ_245984,RMVar_hsa_circ_330263,RMVar_hsa_circ_296676,RMVar_hsa_circ_245986,RMVar_hsa_circ_245988 17840 RMVar_ID_17840 Human_SNP_ID_327111337 A-to-I Human chr7 + 77946864 77946864 77946864 TAAATACTGGCCAGGGACAGTGACTCATGGTTATAATCTTAGCACTTTGGAAGGCCAAGGTGGAT TAAATACTGGCCAGGGACAGTGACTCATGGTTGTAATCTTAGCACTTTGGAAGGCCAAGGTGGAT A G PHTF2 Ensembl:ENSG00000006576 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1137433 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22529405 RMVar_hsa_circ_37844,RMVar_hsa_circ_245982,RMVar_hsa_circ_245978,RMVar_hsa_circ_293654,RMVar_hsa_circ_356350,RMVar_hsa_circ_40818,RMVar_hsa_circ_245984,RMVar_hsa_circ_330263,RMVar_hsa_circ_296676,RMVar_hsa_circ_245986,RMVar_hsa_circ_245988 17841 RMVar_ID_17841 Human_SNP_ID_327113138 A-to-I Human chr7 + 77954396 77954396 77954396 CCTCAAGTGATACACCCACCTTGGCCTCCCAGAGTGCTGGGATTGCAGGTGTGAGCCACCGCGCC CCTCAAGTGATACACCCACCTTGGCCTCCCAGCGTGCTGGGATTGCAGGTGTGAGCCACCGCGCC A C PHTF2 Ensembl:ENSG00000006576 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1371871838 Functional Loss SNV dbSNP153 33..33 33 - - - 17842 RMVar_ID_17842 Human_SNP_ID_327137631 A-to-I Human chr7 - 78054254 78054254 78054254 AGGCGTGGTGATGCACACTTGTAGTCGCAGCTACTCAGGAGGCTGAGGCAGGAGAATAGCTGGAA AGGCGTGGTGATGCACACTTGTAGTCGCAGCTTCTCAGGAGGCTGAGGCAGGAGAATAGCTGGAA T A MAGI2 Ensembl:ENSG00000187391 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1198279360 Functional Loss SNV dbSNP153 33..33 33 - - - 17843 RMVar_ID_17843 Human_SNP_ID_327300936 A-to-I Human chr7 - 78698626 78698626 78698626 CTTTCCTTTGTAAATTACCCAGTTTGGGGTATATCTTTATTAACAGTGTGAGAACAGGCTAATAC CTTTCCTTTGTAAATTACCCAGTTTGGGGTATGTCTTTATTAACAGTGTGAGAACAGGCTAATAC T C MAGI2 Ensembl:ENSG00000187391 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs555764059 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25123 17844 RMVar_ID_17844 Human_SNP_ID_327302684 A-to-I Human chr7 - 78705370 78705370 78705370 TTACTTGACTCACAGTTCCACATGGCTGGGGAAGCCTCAGGAAAATTACAACCATGGCACAAGGC TTACTTGACTCACAGTTCCACATGGCTGGGGAGGCCTCAGGAAAATTACAACCATGGCACAAGGC T C MAGI2 Ensembl:ENSG00000187391 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs549368983 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25123 17845 RMVar_ID_17845 Human_SNP_ID_327307667 A-to-I Human chr7 - 78725625 78725625 78725625 CCGGCTAATTTTTTCTATCTTTTAATAGAGACAGGGTTTCACCGTGTTAGCCAGGATGGTCTCTA CCGGCTAATTTTTTCTATCTTTTAATAGAGACTGGGTTTCACCGTGTTAGCCAGGATGGTCTCTA T A MAGI2 Ensembl:ENSG00000187391 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs890599605 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25123 17846 RMVar_ID_17846 Human_SNP_ID_327316490 A-to-I Human chr7 - 78760439 78760439 78760439 AGAATCGCTCGAACCCAGGAGGTGGAGGTTCAAGTGAGCTGGGATCACACCATTGCACTCCAGCC AGAATCGCTCGAACCCAGGAGGTGGAGGTTCAGGTGAGCTGGGATCACACCATTGCACTCCAGCC T C MAGI2 Ensembl:ENSG00000187391 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1019497414 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25123 17847 RMVar_ID_17847 Human_SNP_ID_327316520 A-to-I Human chr7 - 78760523 78760523 78760523 CCCCATCTCTACTAAAAATACAAAAATTAGCCAGGTACGGTGGTGCATATCTGTAACCCCAGCTA CCCCATCTCTACTAAAAATACAAAAATTAGCCCGGTACGGTGGTGCATATCTGTAACCCCAGCTA T G MAGI2 Ensembl:ENSG00000187391 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1045961723 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25123 17848 RMVar_ID_17848 Human_SNP_ID_327338894 A-to-I Human chr7 - 78853168 78853168 78853168 CCTCACAACCACAAAATGCTGGGATTACAGGCATGAGCCACTGTGCCTGGCCCGTTCTTGATCGA CCTCACAACCACAAAATGCTGGGATTACAGGCGTGAGCCACTGTGCCTGGCCCGTTCTTGATCGA T C MAGI2 Ensembl:ENSG00000187391 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs903653052 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25123 17849 RMVar_ID_17849 Human_SNP_ID_327338895 A-to-I Human chr7 - 78853168 78853168 78853168 CCTCACAACCACAAAATGCTGGGATTACAGGCATGAGCCACTGTGCCTGGCCCGTTCTTGATCGA CCTCACAACCACAAAATGCTGGGATTACAGGCCTGAGCCACTGTGCCTGGCCCGTTCTTGATCGA T G MAGI2 Ensembl:ENSG00000187391 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs903653052 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25123 17850 RMVar_ID_17850 Human_SNP_ID_327449693 A-to-I Human chr7 - 79294091 79294091 79294091 TCACTGCACCCTTTGCCTCCTGTGTTCAAGCAACTCTTTTGCCTCAGCCTCCTGAGGGGATTACA TCACTGCACCCTTTGCCTCCTGTGTTCAAGCACCTCTTTTGCCTCAGCCTCCTGAGGGGATTACA T G MAGI2 Ensembl:ENSG00000187391 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1272384150 Functional Loss SNV dbSNP153 33..33 33 - - - 17851 RMVar_ID_17851 Human_SNP_ID_327457012 A-to-I Human chr7 - 79323064 79323064 79323064 GGAGGCCGAGGTGGGAGGATTGCTTGAGCCCAAGAGTTTGAGACTAGCATGTACAACATAGTGAG GGAGGCCGAGGTGGGAGGATTGCTTGAGCCCAGGAGTTTGAGACTAGCATGTACAACATAGTGAG T C MAGI2 Ensembl:ENSG00000187391 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs957223184 Functional Loss SNV dbSNP153 33..33 33 - - - 17852 RMVar_ID_17852 Human_SNP_ID_327482299 A-to-I Human chr7 - 79425169 79425169 79425169 CGGCTCACTGCAACCTCCGATGCCTGGGTTCAAGCAATTCTCATGACTTAGCCCTCCCAAGCAGC CGGCTCACTGCAACCTCCGATGCCTGGGTTCAGGCAATTCTCATGACTTAGCCCTCCCAAGCAGC T C MAGI2 Ensembl:ENSG00000187391 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1257613365 Functional Loss SNV dbSNP153 33..33 33 - - - 17853 RMVar_ID_17853 Human_SNP_ID_327666092 A-to-I Human chr7 + 80158759 80158759 80158759 ACTGATAGTCACAGTATAAATGGCAAATTACTATTTTCTCAGTTTGCACCACGCTATTCAAGCCA ACTGATAGTCACAGTATAAATGGCAAATTACTGTTTTCTCAGTTTGCACCACGCTATTCAAGCCA A G GNAI1 Ensembl:ENSG00000127955 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1008309641 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21534954 17854 RMVar_ID_17854 Human_SNP_ID_327718875 A-to-I Human chr7 + 80377417 80377417 80377417 TGTGATGCCTTCAGCTTTTTTTTTTTTTTAATATTCTCTTAAGAGTTTATTATAAACCAGTTTCA TGTGATGCCTTCAGCTTTTTTTTTTTTTTAATTTTCTCTTAAGAGTTTATTATAAACCAGTTTCA A T CD36 Ensembl:ENSG00000135218 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1312794689 Functional Loss SNV dbSNP153 33..33 33 - - - 17855 RMVar_ID_17855 Human_SNP_ID_327849181 A-to-I Human chr7 - 80886518 80886518 80886518 GAAACCCCATCTGTACTAAAAATACAAAAATTAGCTGGGTATGGTGGTGCGTGCCTGTAATCCCA GAAACCCCATCTGTACTAAAAATACAAAAATTCGCTGGGTATGGTGGTGCGTGCCTGTAATCCCA T G SEMA3C Ensembl:ENSG00000075223 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1401036103 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25412,RMVar_hsa_circ_91346,RMVar_hsa_circ_246050,RMVar_hsa_circ_26067,RMVar_hsa_circ_342845 17856 RMVar_ID_17856 Human_SNP_ID_328339649 A-to-I Human chr7 - 82853002 82853002 82853002 GCAACAGGGCTGGAATTGGAGGTCATTATGTTAGATGAAATAAGCCAGTCATAGAAAATAAAATA GCAACAGGGCTGGAATTGGAGGTCATTATGTTGGATGAAATAAGCCAGTCATAGAAAATAAAATA T C PCLO Ensembl:ENSG00000186472 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1047228790 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1966,RMVar_hsa_circ_19851,RMVar_hsa_circ_3128,RMVar_hsa_circ_331296,RMVar_hsa_circ_38885,RMVar_hsa_circ_265350,RMVar_hsa_circ_324425,RMVar_hsa_circ_246180 17857 RMVar_ID_17857 Human_SNP_ID_328363457 A-to-I Human chr7 - 82952183 82952182 82952183 ATGAGTCTACTTCAAGTGTGATGACCAAAATAATAGAAGATGAAAAACCCGTTGATTTAACCGCA ATGAGTCTACTTCAAGTGTGATGACCAAAATAGAAGAAGATGAAAAACCCGTTGATTTAACCGCA AT TC PCLO Ensembl:ENSG00000186472 Protein coding CDS GSE56152 embryonic stem cells,wild type - 25708366 RNA-Seq:(High) rs865956001 Functional Loss MNV dbSNP153 33..34 33 - - - Human_RBP_ID_18886377 RMVar_hsa_circ_86878,RMVar_hsa_circ_286580,RMVar_hsa_circ_246188 17858 RMVar_ID_17858 Human_SNP_ID_328399010 A-to-I Human chr7 - 83092802 83092802 83092802 GCTGGGATCTCAGGCACTCATCACCACACCCGACCAACTTTGTATTTTCAGCAGAGACAGGGTTT GCTGGGATCTCAGGCACTCATCACCACACCCGGCCAACTTTGTATTTTCAGCAGAGACAGGGTTT T C PCLO Ensembl:ENSG00000186472 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1409451508 Functional Loss SNV dbSNP153 33..33 33 - - - 17859 RMVar_ID_17859 Human_SNP_ID_328399016 A-to-I Human chr7 - 83092823 83092823 83092823 CCTGCCTCAGCCTCCTGAGTAGCTGGGATCTCAGGCACTCATCACCACACCCGACCAACTTTGTA CCTGCCTCAGCCTCCTGAGTAGCTGGGATCTCGGGCACTCATCACCACACCCGACCAACTTTGTA T C PCLO Ensembl:ENSG00000186472 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs533166842 Functional Loss SNV dbSNP153 33..33 33 - - - 17860 RMVar_ID_17860 Human_SNP_ID_328399623 A-to-I Human chr7 - 83094337 83094337 83094337 GGGCATGGTGGCGCACACCTGTAGTCCCAGCTACTTGGGCAGCTGAGGCAGGAGAATCGCTTGAA GGGCATGGTGGCGCACACCTGTAGTCCCAGCTGCTTGGGCAGCTGAGGCAGGAGAATCGCTTGAA T C PCLO Ensembl:ENSG00000186472 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1194808843 Functional Loss SNV dbSNP153 33..33 33 - - - 17861 RMVar_ID_17861 Human_SNP_ID_329383725 A-to-I Human chr7 - 87049414 87049414 87049414 AGCCAGGCATGGTGGCGGGAGCCTGTGGTTCCAGCTGCTCGGGAGGCTGAGGCAGGAGAATGGCG AGCCAGGCATGGTGGCGGGAGCCTGTGGTTCCGGCTGCTCGGGAGGCTGAGGCAGGAGAATGGCG T C KIAA1324L Ensembl:ENSG00000164659 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs959474169 Functional Loss SNV dbSNP153 33..33 33 - - - 17862 RMVar_ID_17862 Human_SNP_ID_329409547 A-to-I Human chr7 + 87160514 87160514 87160514 CCAGGCGGGTTTCGAACTCCTGACCTCAGGTGATCTTCCTGCCTCGGCCTCCCAAAGTGCTGGGA CCAGGCGGGTTTCGAACTCCTGACCTCAGGTGGTCTTCCTGCCTCGGCCTCCCAAAGTGCTGGGA A G DMTF1 Ensembl:ENSG00000135164 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968782323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16233707,Human_RBP_ID_23198615,Human_RBP_ID_26139403 RMVar_hsa_circ_313994,RMVar_hsa_circ_340846,RMVar_hsa_circ_246234 17863 RMVar_ID_17863 Human_SNP_ID_329409774 A-to-I Human chr7 + 87161234 87161234 87161234 ATTTAGGATGACGGGACCAGGCACATTGGCTCACGCCTGTAATCCCAACACTTTGGGAGGCCGAG ATTTAGGATGACGGGACCAGGCACATTGGCTCCCGCCTGTAATCCCAACACTTTGGGAGGCCGAG A C DMTF1 Ensembl:ENSG00000135164 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1475254651 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16233739 RMVar_hsa_circ_313994,RMVar_hsa_circ_340846,RMVar_hsa_circ_246234 17864 RMVar_ID_17864 Human_SNP_ID_329409822 A-to-I Human chr7 + 87161351 87161351 87161351 GAAACCCCATCTCTACTAAAAAAATACCAAAAAATTAGCTGGGCATGGTGGCACACGCCTGTAGT GAAACCCCATCTCTACTAAAAAAATACCAAAATATTAGCTGGGCATGGTGGCACACGCCTGTAGT A T DMTF1 Ensembl:ENSG00000135164 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs534514685 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_313994,RMVar_hsa_circ_340846,RMVar_hsa_circ_246234 17865 RMVar_ID_17865 Human_SNP_ID_329410038 A-to-I Human chr7 + 87162186 87162186 87162186 GCCTTGATCTCCTGGGCTGCAGCCATCCTCCCACCTCAGCCTCCAGAGTAGCTGAGATTATAGGC GCCTTGATCTCCTGGGCTGCAGCCATCCTCCCGCCTCAGCCTCCAGAGTAGCTGAGATTATAGGC A G DMTF1 Ensembl:ENSG00000135164 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1199557267 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7764253,Human_RBP_ID_16233777 RMVar_hsa_circ_313994,RMVar_hsa_circ_340846,RMVar_hsa_circ_246234 17866 RMVar_ID_17866 Human_SNP_ID_329410047 A-to-I Human chr7 + 87162223 87162223 87162223 AGCCTCCAGAGTAGCTGAGATTATAGGCATACACCACCACACCTGGCTAATTTTTTATTTTTTTT AGCCTCCAGAGTAGCTGAGATTATAGGCATACGCCACCACACCTGGCTAATTTTTTATTTTTTTT A G DMTF1 Ensembl:ENSG00000135164 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1246667120 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_313994,RMVar_hsa_circ_340846,RMVar_hsa_circ_246234 17867 RMVar_ID_17867 Human_SNP_ID_329410054 A-to-I Human chr7 + 87162239 87162239 87162239 GAGATTATAGGCATACACCACCACACCTGGCTAATTTTTTATTTTTTTTCTGGAGACTAGATCTC GAGATTATAGGCATACACCACCACACCTGGCTGATTTTTTATTTTTTTTCTGGAGACTAGATCTC A G DMTF1 Ensembl:ENSG00000135164 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1409686915 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_313994,RMVar_hsa_circ_340846,RMVar_hsa_circ_246234 17868 RMVar_ID_17868 Human_SNP_ID_329410056 A-to-I Human chr7 + 87162247 87162247 87162247 AGGCATACACCACCACACCTGGCTAATTTTTTATTTTTTTTCTGGAGACTAGATCTCACTATCTC AGGCATACACCACCACACCTGGCTAATTTTTTTTTTTTTTTCTGGAGACTAGATCTCACTATCTC A T DMTF1 Ensembl:ENSG00000135164 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs577059815 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3107491,Human_RBP_ID_10363728,Human_RBP_ID_16233780 RMVar_hsa_circ_313994,RMVar_hsa_circ_340846,RMVar_hsa_circ_246234 17869 RMVar_ID_17869 Human_SNP_ID_329410074 A-to-I Human chr7 + 87162292 87162292 87162292 AGACTAGATCTCACTATCTCAGGCTGGTCTCAAACTCCTGAGGTTAAGTGATCCTCCTCCCAAAG AGACTAGATCTCACTATCTCAGGCTGGTCTCAGACTCCTGAGGTTAAGTGATCCTCCTCCCAAAG A G DMTF1 Ensembl:ENSG00000135164 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1037749986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22620588 RMVar_hsa_circ_313994,RMVar_hsa_circ_340846,RMVar_hsa_circ_246234 17870 RMVar_ID_17870 Human_SNP_ID_329410078 A-to-I Human chr7 + 87162305 87162305 87162305 CTATCTCAGGCTGGTCTCAAACTCCTGAGGTTAAGTGATCCTCCTCCCAAAGTGCTGGGATTATA CTATCTCAGGCTGGTCTCAAACTCCTGAGGTTGAGTGATCCTCCTCCCAAAGTGCTGGGATTATA A G DMTF1 Ensembl:ENSG00000135164 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1041415223 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_313994,RMVar_hsa_circ_340846,RMVar_hsa_circ_246234 17871 RMVar_ID_17871 Human_SNP_ID_329416101 A-to-I Human chr7 + 87186449 87186449 87186449 GCTATTTTTTTTCGTAGAGATGAGGTCTTGCCATGTTACCCAGGTTGGTCTCCAACTCCTGGGCT GCTATTTTTTTTCGTAGAGATGAGGTCTTGCCGTGTTACCCAGGTTGGTCTCCAACTCCTGGGCT A G DMTF1 Ensembl:ENSG00000135164 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1213360685 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8672769 RMVar_hsa_circ_340846,RMVar_hsa_circ_246234,RMVar_hsa_circ_331489,RMVar_hsa_circ_323539,RMVar_hsa_circ_39179,RMVar_hsa_circ_273576,RMVar_hsa_circ_246237,RMVar_hsa_circ_246236,RMVar_hsa_circ_29530,RMVar_hsa_circ_246244,RMVar_hsa_circ_25678,RMVar_hsa_circ_321491,RMVar_hsa_circ_31913,RMVar_hsa_circ_246247,RMVar_hsa_circ_7236 17872 RMVar_ID_17872 Human_SNP_ID_329416294 A-to-I Human chr7 + 87187305 87187305 87187305 CCTATAATCCCAGTACTGTGGGAGGCCAAGGCAGGAGGATCACTTGACGCTAGGAGTTTGAGACC CCTATAATCCCAGTACTGTGGGAGGCCAAGGCCGGAGGATCACTTGACGCTAGGAGTTTGAGACC A C DMTF1 Ensembl:ENSG00000135164 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1234705458 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_340846,RMVar_hsa_circ_246234,RMVar_hsa_circ_331489,RMVar_hsa_circ_323539,RMVar_hsa_circ_39179,RMVar_hsa_circ_273576,RMVar_hsa_circ_246237,RMVar_hsa_circ_246236,RMVar_hsa_circ_29530,RMVar_hsa_circ_246244,RMVar_hsa_circ_25678,RMVar_hsa_circ_321491,RMVar_hsa_circ_31913,RMVar_hsa_circ_246247,RMVar_hsa_circ_7236 17873 RMVar_ID_17873 Human_SNP_ID_329416303 A-to-I Human chr7 + 87187350 87187350 87187350 GACGCTAGGAGTTTGAGACCAGCCTGGGCAACATAGCAAGACCCCATTACTACAGAAAAAATAAA GACGCTAGGAGTTTGAGACCAGCCTGGGCAACCTAGCAAGACCCCATTACTACAGAAAAAATAAA A C DMTF1 Ensembl:ENSG00000135164 Protein coding intron GSE47997;GSE107867 K562 cells&HepG2 cells;ASD brains,temporal_cortex - 23474544,30559470 RNA-Seq:(High) rs1386038630 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_340846,RMVar_hsa_circ_246234,RMVar_hsa_circ_331489,RMVar_hsa_circ_323539,RMVar_hsa_circ_39179,RMVar_hsa_circ_273576,RMVar_hsa_circ_246237,RMVar_hsa_circ_246236,RMVar_hsa_circ_29530,RMVar_hsa_circ_246244,RMVar_hsa_circ_25678,RMVar_hsa_circ_321491,RMVar_hsa_circ_31913,RMVar_hsa_circ_246247,RMVar_hsa_circ_7236 17874 RMVar_ID_17874 Human_SNP_ID_329416309 A-to-I Human chr7 + 87187395 87187395 87187395 ATTACTACAGAAAAAATAAAAACCAATTAGCCAGGCATGGTGGGCATGTGCTTGTAGTCCCAGCT ATTACTACAGAAAAAATAAAAACCAATTAGCCGGGCATGGTGGGCATGTGCTTGTAGTCCCAGCT A G DMTF1 Ensembl:ENSG00000135164 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs929789501 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7764494,Human_RBP_ID_17577482 RMVar_hsa_circ_340846,RMVar_hsa_circ_246234,RMVar_hsa_circ_331489,RMVar_hsa_circ_323539,RMVar_hsa_circ_39179,RMVar_hsa_circ_273576,RMVar_hsa_circ_246237,RMVar_hsa_circ_246236,RMVar_hsa_circ_29530,RMVar_hsa_circ_246244,RMVar_hsa_circ_25678,RMVar_hsa_circ_321491,RMVar_hsa_circ_31913,RMVar_hsa_circ_246247,RMVar_hsa_circ_7236 17875 RMVar_ID_17875 Human_SNP_ID_329416315 A-to-I Human chr7 + 87187418 87187418 87187418 CAATTAGCCAGGCATGGTGGGCATGTGCTTGTAGTCCCAGCTATTGGGGAGCAAGAGCCTGAGGC CAATTAGCCAGGCATGGTGGGCATGTGCTTGTGGTCCCAGCTATTGGGGAGCAAGAGCCTGAGGC A G DMTF1 Ensembl:ENSG00000135164 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048157907 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7764494,Human_RBP_ID_17577482 RMVar_hsa_circ_340846,RMVar_hsa_circ_246234,RMVar_hsa_circ_331489,RMVar_hsa_circ_323539,RMVar_hsa_circ_39179,RMVar_hsa_circ_273576,RMVar_hsa_circ_246237,RMVar_hsa_circ_246236,RMVar_hsa_circ_29530,RMVar_hsa_circ_246244,RMVar_hsa_circ_25678,RMVar_hsa_circ_321491,RMVar_hsa_circ_31913,RMVar_hsa_circ_246247,RMVar_hsa_circ_7236 17876 RMVar_ID_17876 Human_SNP_ID_329462959 A-to-I Human chr7 + 87371857 87371857 87371857 TATAAAAAGTTAAAAAATTAGCTGGACATGATAGTGCTACTTGGGAGTGCTCCCAGCTACTTGGA TATAAAAAGTTAAAAAATTAGCTGGACATGATTGTGCTACTTGGGAGTGCTCCCAGCTACTTGGA A T CROT Ensembl:ENSG00000005469 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1267077033 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2907,RMVar_hsa_circ_73711,RMVar_hsa_circ_273281,RMVar_hsa_circ_311541,RMVar_hsa_circ_297057,RMVar_hsa_circ_268952,RMVar_hsa_circ_1488,RMVar_hsa_circ_246252,RMVar_hsa_circ_246253,RMVar_hsa_circ_246251,RMVar_hsa_circ_246255,RMVar_hsa_circ_318509 17877 RMVar_ID_17877 Human_SNP_ID_329572034 A-to-I Human chr7 - 87835340 87835340 87835340 TTGTTCTAACAAGACAGATTATTGCTACAACAATAGTTACAAGATATTTCTAAAATATCCTTTGA TTGTTCTAACAAGACAGATTATTGCTACAACAGTAGTTACAAGATATTTCTAAAATATCCTTTGA T C SLC25A40 Ensembl:ENSG00000075303 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs754048563 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_689187,Human_RBP_ID_17314624,Human_RBP_ID_24229707 Human_miRNA_ID_840013 RMVar_hsa_circ_90344,RMVar_hsa_circ_246281 17878 RMVar_ID_17878 Human_SNP_ID_329585171 A-to-I Human chr7 + 87889297 87889297 87889297 AACTCTTGAACAATTTTTTTTTTTTTTTTTTGAGGCAGGCCCTCCCCCTCTGTCATCCAGGCTGG AACTCTTGAACAATTTTTTTTTTTTTTTTTTGTGGCAGGCCCTCCCCCTCTGTCATCCAGGCTGG A T DBF4 Ensembl:ENSG00000006634 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1274942391 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_254083,Human_RBP_ID_794745,Human_RBP_ID_16236430 RMVar_hsa_circ_10076,RMVar_hsa_circ_307413,RMVar_hsa_circ_367703 17879 RMVar_ID_17879 Human_SNP_ID_329585278 A-to-I Human chr7 + 87889747 87889745 87889747 ACAAAGTAGTATTTAAATAAAACTATCAATCAAAGTGTAAAAATGATTTGGAAAACTGGTCAGAA ACAAAGTAGTATTTAAATAAAACTATCAATC__AGTGTAAAAATGATTTGGAAAACTGGTCAGAA CAA C DBF4 Ensembl:ENSG00000006634 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs937573102 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_3107935,Human_RBP_ID_7765185,Human_RBP_ID_8148359,Human_RBP_ID_17050383 RMVar_hsa_circ_10076,RMVar_hsa_circ_307413,RMVar_hsa_circ_367703 17880 RMVar_ID_17880 Human_SNP_ID_329585281 A-to-I Human chr7 + 87889747 87889747 87889747 ACAAAGTAGTATTTAAATAAAACTATCAATCAAAGTGTAAAAATGATTTGGAAAACTGGTCAGAA ACAAAGTAGTATTTAAATAAAACTATCAATCATAGTGTAAAAATGATTTGGAAAACTGGTCAGAA A T DBF4 Ensembl:ENSG00000006634 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1044499570 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3107935,Human_RBP_ID_7765185,Human_RBP_ID_8148359,Human_RBP_ID_17050383 RMVar_hsa_circ_10076,RMVar_hsa_circ_307413,RMVar_hsa_circ_367703 17881 RMVar_ID_17881 Human_SNP_ID_329587273 A-to-I Human chr7 + 87897881 87897881 87897881 ACTGCAACGTCCACCCCACCCCCGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGG ACTGCAACGTCCACCCCACCCCCGGTTCAAGCCATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGG A C DBF4 Ensembl:ENSG00000006634 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1233734022 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10076 17882 RMVar_ID_17882 Human_SNP_ID_329587299 A-to-I Human chr7 + 87897978 87897978 87897978 GTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTAGTCTCTAACTCTTGACCT GTTTGTATTTTTAGTAGAGATGGGGTTTCACCTTGTTGGCCAGGCTAGTCTCTAACTCTTGACCT A T DBF4 Ensembl:ENSG00000006634 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs545447805 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10076 17883 RMVar_ID_17883 Human_SNP_ID_329587306 A-to-I Human chr7 + 87897992 87897992 87897992 TAGAGATGGGGTTTCACCATGTTGGCCAGGCTAGTCTCTAACTCTTGACCTCAAGTGATCCGCCT TAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTCTAACTCTTGACCTCAAGTGATCCGCCT A G DBF4 Ensembl:ENSG00000006634 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs369419705 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10076 17884 RMVar_ID_17884 Human_SNP_ID_329652658 A-to-I Human chr7 + 88169107 88169107 88169107 ATTATCACTTAACATGGTCTTAAACCAATTGCACCAAAGGAAACATCTTTATAGTGTACATGGTA ATTATCACTTAACATGGTCTTAAACCAATTGCTCCAAAGGAAACATCTTTATAGTGTACATGGTA A T ADAM22 Ensembl:ENSG00000008277 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1233673330 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6668,RMVar_hsa_circ_23684,RMVar_hsa_circ_25590,RMVar_hsa_circ_321232,RMVar_hsa_circ_246293,RMVar_hsa_circ_266276,RMVar_hsa_circ_268230,RMVar_hsa_circ_314330,RMVar_hsa_circ_267517,RMVar_hsa_circ_10707,RMVar_hsa_circ_116454,RMVar_hsa_circ_246297 17885 RMVar_ID_17885 Human_SNP_ID_329652667 A-to-I Human chr7 + 88169134 88169134 88169134 ATTGCACCAAAGGAAACATCTTTATAGTGTACATGGTAATTGCTTGTGAGGTCAAAACCATCAAA ATTGCACCAAAGGAAACATCTTTATAGTGTACGTGGTAATTGCTTGTGAGGTCAAAACCATCAAA A G ADAM22 Ensembl:ENSG00000008277 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1057182360 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6668,RMVar_hsa_circ_23684,RMVar_hsa_circ_25590,RMVar_hsa_circ_321232,RMVar_hsa_circ_246293,RMVar_hsa_circ_266276,RMVar_hsa_circ_268230,RMVar_hsa_circ_314330,RMVar_hsa_circ_267517,RMVar_hsa_circ_10707,RMVar_hsa_circ_116454,RMVar_hsa_circ_246297 17886 RMVar_ID_17886 Human_SNP_ID_329652681 A-to-I Human chr7 + 88169198 88169198 88169198 AGAGTTTCTTTGGCTAAAAAGGGAGAGCAGTTAGTTTACTGGCAGGATAAGCTTTGTATGCTGCA AGAGTTTCTTTGGCTAAAAAGGGAGAGCAGTTCGTTTACTGGCAGGATAAGCTTTGTATGCTGCA A C ADAM22 Ensembl:ENSG00000008277 Protein coding intron GSE107867 ASD brains,cerebellum;ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1469932480 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6668,RMVar_hsa_circ_23684,RMVar_hsa_circ_25590,RMVar_hsa_circ_321232,RMVar_hsa_circ_246293,RMVar_hsa_circ_266276,RMVar_hsa_circ_268230,RMVar_hsa_circ_314330,RMVar_hsa_circ_267517,RMVar_hsa_circ_10707,RMVar_hsa_circ_116454,RMVar_hsa_circ_246297 17887 RMVar_ID_17887 Human_SNP_ID_329652689 A-to-I Human chr7 + 88169223 88169223 88169223 AGCAGTTAGTTTACTGGCAGGATAAGCTTTGTATGCTGCAAGCATTAATAATACAGGCATTTGTG AGCAGTTAGTTTACTGGCAGGATAAGCTTTGTGTGCTGCAAGCATTAATAATACAGGCATTTGTG A G ADAM22 Ensembl:ENSG00000008277 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1378318789 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8148370 RMVar_hsa_circ_6668,RMVar_hsa_circ_23684,RMVar_hsa_circ_25590,RMVar_hsa_circ_321232,RMVar_hsa_circ_246293,RMVar_hsa_circ_266276,RMVar_hsa_circ_268230,RMVar_hsa_circ_314330,RMVar_hsa_circ_267517,RMVar_hsa_circ_10707,RMVar_hsa_circ_116454,RMVar_hsa_circ_246297 17888 RMVar_ID_17888 Human_SNP_ID_329652734 A-to-I Human chr7 + 88169426 88169426 88169426 GTACCATGTAGTCTTCCACAAATTCTTGTATCATTAATGCTTGTAGCATACAAAACTTATCCTGG GTACCATGTAGTCTTCCACAAATTCTTGTATCGTTAATGCTTGTAGCATACAAAACTTATCCTGG A G ADAM22 Ensembl:ENSG00000008277 Protein coding intron GSE107867 ASD brains,cerebellum;ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1466116239 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6668,RMVar_hsa_circ_23684,RMVar_hsa_circ_25590,RMVar_hsa_circ_321232,RMVar_hsa_circ_246293,RMVar_hsa_circ_266276,RMVar_hsa_circ_268230,RMVar_hsa_circ_314330,RMVar_hsa_circ_267517,RMVar_hsa_circ_10707,RMVar_hsa_circ_116454,RMVar_hsa_circ_246297 17889 RMVar_ID_17889 Human_SNP_ID_329659504 A-to-I Human chr7 - 88201251 88201251 88201251 AGATAAAGATGCCTGCCACCTCTACTCCCTAGAGCATCCTAGGGATATAAAGGACAAAAGTACTA AGATAAAGATGCCTGCCACCTCTACTCCCTAGGGCATCCTAGGGATATAAAGGACAAAAGTACTA T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs79257858 Functional Loss SNV dbSNP153 33..33 33 - - - 17890 RMVar_ID_17890 Human_SNP_ID_190141769 A-to-I Human chr4 - 75585492 75585492 75585492 AATTCCTAGGATCAAGCGATCTTCCCCCATCAACCTCCTGAGTAACTAAGACTACAGGCACAGCT AATTCCTAGGATCAAGCGATCTTCCCCCATCAGCCTCCTGAGTAACTAAGACTACAGGCACAGCT T C CDKL2 Ensembl:ENSG00000138769 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs565587323 Functional Loss SNV dbSNP153 33..33 33 - - - 17891 RMVar_ID_17891 Human_SNP_ID_190184601 A-to-I Human chr4 + 75756680 75756678 75756681 AGGCATGCACCACCACGCCCGGCTAATTTTGTATTTTTAATAGAGACGGGGTTTCTCCGTCTCTA AGGCATGCACCACCACGCCCGGCTAATTTTG___TTTTAATAGAGACGGGGTTTCTCCGTCTCTA GTAT G USO1 Ensembl:ENSG00000138768 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1388286653 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_9693,RMVar_hsa_circ_46820,RMVar_hsa_circ_343296,RMVar_hsa_circ_302786 17892 RMVar_ID_17892 Human_SNP_ID_190184602 A-to-I Human chr4 + 75756680 75756680 75756680 AGGCATGCACCACCACGCCCGGCTAATTTTGTATTTTTAATAGAGACGGGGTTTCTCCGTCTCTA AGGCATGCACCACCACGCCCGGCTAATTTTGTGTTTTTAATAGAGACGGGGTTTCTCCGTCTCTA A G USO1 Ensembl:ENSG00000138768 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1308529345 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9693,RMVar_hsa_circ_46820,RMVar_hsa_circ_343296,RMVar_hsa_circ_302786 17893 RMVar_ID_17893 Human_SNP_ID_190186026 A-to-I Human chr4 + 75762436 75762422 75762437 CGCCCTTCTTGGCCTCCCAAAGTGTTGGGATTACAGGCATGAGCCACCACGCCCAGCCAGAACAA CGCCCTTCTTGGCCTCCCA_______________AGGCATGAGCCACCACGCCCAGCCAGAACAA AAAGTGTTGGGATTAC A USO1 Ensembl:ENSG00000138768 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417091374 Functional Loss DEL dbSNP153 20..34 33 - - - RMVar_hsa_circ_9693,RMVar_hsa_circ_46820,RMVar_hsa_circ_343296,RMVar_hsa_circ_26680,RMVar_hsa_circ_349075,RMVar_hsa_circ_266781,RMVar_hsa_circ_107338,RMVar_hsa_circ_226633 17894 RMVar_ID_17894 Human_SNP_ID_190193222 A-to-I Human chr4 + 75792608 75792608 75792608 AGTCCTAGCTACATGGGAGGCTGAGGTGCGAGAATCACCTGAGCCTGGGAGGTCGAGGCTGCAGT AGTCCTAGCTACATGGGAGGCTGAGGTGCGAGGATCACCTGAGCCTGGGAGGTCGAGGCTGCAGT A G USO1 Ensembl:ENSG00000138768 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1008048301 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17575142 RMVar_hsa_circ_4046,RMVar_hsa_circ_320980,RMVar_hsa_circ_266781,RMVar_hsa_circ_107338,RMVar_hsa_circ_226633,RMVar_hsa_circ_63650,RMVar_hsa_circ_226637,RMVar_hsa_circ_49445,RMVar_hsa_circ_82353,RMVar_hsa_circ_86823,RMVar_hsa_circ_226639,RMVar_hsa_circ_226640,RMVar_hsa_circ_118223,RMVar_hsa_circ_62708,RMVar_hsa_circ_226642,RMVar_hsa_circ_364071 17895 RMVar_ID_17895 Human_SNP_ID_190193223 A-to-I Human chr4 + 75792612 75792612 75792612 CTAGCTACATGGGAGGCTGAGGTGCGAGAATCACCTGAGCCTGGGAGGTCGAGGCTGCAGTGAAC CTAGCTACATGGGAGGCTGAGGTGCGAGAATCTCCTGAGCCTGGGAGGTCGAGGCTGCAGTGAAC A T USO1 Ensembl:ENSG00000138768 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1385869092 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17575142 RMVar_hsa_circ_4046,RMVar_hsa_circ_320980,RMVar_hsa_circ_266781,RMVar_hsa_circ_107338,RMVar_hsa_circ_226633,RMVar_hsa_circ_63650,RMVar_hsa_circ_226637,RMVar_hsa_circ_49445,RMVar_hsa_circ_82353,RMVar_hsa_circ_86823,RMVar_hsa_circ_226639,RMVar_hsa_circ_226640,RMVar_hsa_circ_118223,RMVar_hsa_circ_62708,RMVar_hsa_circ_226642,RMVar_hsa_circ_364071 17896 RMVar_ID_17896 Human_SNP_ID_190195607 A-to-I Human chr4 + 75801999 75801999 75801999 GTGCCACCACGCTGCCTAATTTTTATATTTTTAGTAGAGATGAGGTTTCACCATGTTGGCTGGTG GTGCCACCACGCTGCCTAATTTTTATATTTTTTGTAGAGATGAGGTTTCACCATGTTGGCTGGTG A T USO1 Ensembl:ENSG00000138768 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1021034881 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4046,RMVar_hsa_circ_266781,RMVar_hsa_circ_63650,RMVar_hsa_circ_41948,RMVar_hsa_circ_62708,RMVar_hsa_circ_47750,RMVar_hsa_circ_49853,RMVar_hsa_circ_5691,RMVar_hsa_circ_315211,RMVar_hsa_circ_77063,RMVar_hsa_circ_226644,RMVar_hsa_circ_226645,RMVar_hsa_circ_46436,RMVar_hsa_circ_226646 17897 RMVar_ID_17897 Human_SNP_ID_190196680 A-to-I Human chr4 + 75806172 75806172 75806172 CGCTGCCACGTCCGGCTAATTTTTTGTATTTTAGTAGAGATAGGGTTTCACCGTGTTGCCCAAGC CGCTGCCACGTCCGGCTAATTTTTTGTATTTTGGTAGAGATAGGGTTTCACCGTGTTGCCCAAGC A G USO1 Ensembl:ENSG00000138768 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs961284306 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4046,RMVar_hsa_circ_63650,RMVar_hsa_circ_41948,RMVar_hsa_circ_47750,RMVar_hsa_circ_5691,RMVar_hsa_circ_37281,RMVar_hsa_circ_77063,RMVar_hsa_circ_226644,RMVar_hsa_circ_226646,RMVar_hsa_circ_349434 17898 RMVar_ID_17898 Human_SNP_ID_190196695 A-to-I Human chr4 + 75806226 75806226 75806226 GTTGCCCAAGCTGATCTTGCATTCCTGAGCTCAAGCAATCCACTGGCCTTGGCCTCCCAAGGATT GTTGCCCAAGCTGATCTTGCATTCCTGAGCTCCAGCAATCCACTGGCCTTGGCCTCCCAAGGATT A C USO1 Ensembl:ENSG00000138768 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1242332593 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4046,RMVar_hsa_circ_63650,RMVar_hsa_circ_41948,RMVar_hsa_circ_47750,RMVar_hsa_circ_5691,RMVar_hsa_circ_37281,RMVar_hsa_circ_77063,RMVar_hsa_circ_226644,RMVar_hsa_circ_226646,RMVar_hsa_circ_349434 17899 RMVar_ID_17899 Human_SNP_ID_190224929 A-to-I Human chr4 - 75916917 75916917 75916917 AAATTAGCCAGGCGTCATGGTGCGTGCCTGTAATCCCAGCTACTTGGGAGGTGGAGGCAGGAAAA AAATTAGCCAGGCGTCATGGTGCGTGCCTGTAGTCCCAGCTACTTGGGAGGTGGAGGCAGGAAAA T C NAAA Ensembl:ENSG00000138744 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1136958 Functional Loss SNV dbSNP153 33..33 33 - - - 17900 RMVar_ID_17900 Human_SNP_ID_190225084 A-to-I Human chr4 - 75917586 75917586 75917586 CGGTGCACGCCTGTTATCACAGCTACTTGGGAAGCAGCGGCTGGAGAATTGCTTGAACCTGGGAA CGGTGCACGCCTGTTATCACAGCTACTTGGGAGGCAGCGGCTGGAGAATTGCTTGAACCTGGGAA T C NAAA Ensembl:ENSG00000138744 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs116622151 Functional Loss SNV dbSNP153 33..33 33 - - - 17901 RMVar_ID_17901 Human_SNP_ID_190225088 A-to-I Human chr4 - 75917603 75917603 75917603 AAATCAACCAGGCATGACGGTGCACGCCTGTTATCACAGCTACTTGGGAAGCAGCGGCTGGAGAA AAATCAACCAGGCATGACGGTGCACGCCTGTTGTCACAGCTACTTGGGAAGCAGCGGCTGGAGAA T C NAAA Ensembl:ENSG00000138744 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs938838479 Functional Loss SNV dbSNP153 33..33 33 - - - 17902 RMVar_ID_17902 Human_SNP_ID_190225105 A-to-I Human chr4 - 75917659 75917659 75917659 GAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCTCGTCTCTACTAAAAATACAAAAATCAACC GAGTTCAAGACCAGCCTGGCCAACATGGTGAACCCTCGTCTCTACTAAAAATACAAAAATCAACC T G NAAA Ensembl:ENSG00000138744 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1043073207 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_162375 17903 RMVar_ID_17903 Human_SNP_ID_190232694 A-to-I Human chr4 + 75947534 75947534 75947534 CCTGCTTCAGCCTCCTGAGTAGCTGGTATGGCAAGCATGCACCATCACACCTGGCTAATTTTTAC CCTGCTTCAGCCTCCTGAGTAGCTGGTATGGCCAGCATGCACCATCACACCTGGCTAATTTTTAC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1284487279 Functional Loss SNV dbSNP153 33..33 33 - - - 17904 RMVar_ID_17904 Human_SNP_ID_190275811 A-to-I Human chr4 - 76118667 76118667 76118667 TGTTGGCTTGGCAAAGTGGCTCACACCTGTAAACCCAGCACTCTGGGAGGCCAAGGCTAGAGGAT TGTTGGCTTGGCAAAGTGGCTCACACCTGTAATCCCAGCACTCTGGGAGGCCAAGGCTAGAGGAT T A NUP54 Ensembl:ENSG00000138750 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1370974771 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17574791 RMVar_hsa_circ_226673,RMVar_hsa_circ_355334,RMVar_hsa_circ_226671,RMVar_hsa_circ_118040,RMVar_hsa_circ_226672,RMVar_hsa_circ_267880,RMVar_hsa_circ_269406,RMVar_hsa_circ_265070,RMVar_hsa_circ_304550 17905 RMVar_ID_17905 Human_SNP_ID_190275812 A-to-I Human chr4 - 76118667 76118667 76118667 TGTTGGCTTGGCAAAGTGGCTCACACCTGTAAACCCAGCACTCTGGGAGGCCAAGGCTAGAGGAT TGTTGGCTTGGCAAAGTGGCTCACACCTGTAAGCCCAGCACTCTGGGAGGCCAAGGCTAGAGGAT T C NUP54 Ensembl:ENSG00000138750 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1370974771 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17574791 RMVar_hsa_circ_226673,RMVar_hsa_circ_355334,RMVar_hsa_circ_226671,RMVar_hsa_circ_118040,RMVar_hsa_circ_226672,RMVar_hsa_circ_267880,RMVar_hsa_circ_269406,RMVar_hsa_circ_265070,RMVar_hsa_circ_304550 17906 RMVar_ID_17906 Human_SNP_ID_190275881 A-to-I Human chr4 - 76118866 76118864 76118867 CGAGTAGCTGGGACTACAGGCGTGCACCATCAACGTCCGGCTAATTTTTTGTATTTTTAGTAGAG CGAGTAGCTGGGACTACAGGCGTGCACCATC___GTCCGGCTAATTTTTTGTATTTTTAGTAGAG CGTT C NUP54 Ensembl:ENSG00000138750 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1364943336 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_226673,RMVar_hsa_circ_355334,RMVar_hsa_circ_226671,RMVar_hsa_circ_118040,RMVar_hsa_circ_226672,RMVar_hsa_circ_267880,RMVar_hsa_circ_269406,RMVar_hsa_circ_265070,RMVar_hsa_circ_304550 17907 RMVar_ID_17907 Human_SNP_ID_190275884 A-to-I Human chr4 - 76118866 76118865 76118866 CGAGTAGCTGGGACTACAGGCGTGCACCATCAACGTCCGGCTAATTTTTTGTATTTTTAGTAGAG CGAGTAGCTGGGACTACAGGCGTGCACCATCA_CGTCCGGCTAATTTTTTGTATTTTTAGTAGAG GT G NUP54 Ensembl:ENSG00000138750 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1560673721 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_226673,RMVar_hsa_circ_355334,RMVar_hsa_circ_226671,RMVar_hsa_circ_118040,RMVar_hsa_circ_226672,RMVar_hsa_circ_267880,RMVar_hsa_circ_269406,RMVar_hsa_circ_265070,RMVar_hsa_circ_304550 17908 RMVar_ID_17908 Human_SNP_ID_190275886 A-to-I Human chr4 - 76118866 76118866 76118866 CGAGTAGCTGGGACTACAGGCGTGCACCATCAACGTCCGGCTAATTTTTTGTATTTTTAGTAGAG CGAGTAGCTGGGACTACAGGCGTGCACCATCATCGTCCGGCTAATTTTTTGTATTTTTAGTAGAG T A NUP54 Ensembl:ENSG00000138750 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1383400480 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_226673,RMVar_hsa_circ_355334,RMVar_hsa_circ_226671,RMVar_hsa_circ_118040,RMVar_hsa_circ_226672,RMVar_hsa_circ_267880,RMVar_hsa_circ_269406,RMVar_hsa_circ_265070,RMVar_hsa_circ_304550 17909 RMVar_ID_17909 Human_SNP_ID_190286417 A-to-I Human chr4 - 76159707 76159707 76159707 TGTCATGATTCTTTTTTTTTTGAGAGAGTCTCACTCTGTCGCCAGGCTGGAGTACAGTGGCATGA TGTCATGATTCTTTTTTTTTTGAGAGAGTCTCTCTCTGTCGCCAGGCTGGAGTACAGTGGCATGA T A SCARB2 Ensembl:ENSG00000138760 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1024764741 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_867512,Human_miRNA_ID_2972754,Human_miRNA_ID_3005939 RMVar_hsa_circ_86190,RMVar_hsa_circ_122685,RMVar_hsa_circ_226688,RMVar_hsa_circ_226689 17910 RMVar_ID_17910 Human_SNP_ID_190459206 A-to-I Human chr4 - 76906440 76906439 76906441 GAAGCTTCCTGGGGCCTCCCTAGAAGCCAAGCAGATGCCAGCATCATGCTTCCTGTAAAGCCTAC GAAGCTTCCTGGGGCCTCCCTAGAAGCCAAG__GATGCCAGCATCATGCTTCCTGTAAAGCCTAC CTG C lnc-SOWAHB-5,lnc-SOWAHB-5:2 RNACentral:URS0000D5C032,RNACentral:URS0000D58B58 lincRNA,lincRNA exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1407062462 Functional Loss DEL dbSNP153 32..33 33 - - - 17911 RMVar_ID_17911 Human_SNP_ID_190463453 A-to-I Human chr4 + 76922723 76922723 76922723 TGTTTGTTTGTTTTTAGACTGTCACCCAGGCTAGAGTGCAGTGGCATGATTTCAGTTCTCTGCAA TGTTTGTTTGTTTTTAGACTGTCACCCAGGCTGGAGTGCAGTGGCATGATTTCAGTTCTCTGCAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs937808504 Functional Loss SNV dbSNP153 33..33 33 - - - 17912 RMVar_ID_17912 Human_SNP_ID_190467828 A-to-I Human chr4 - 76942869 76942869 76942869 TACCTGCCTCGGCCTCCCAAAATGCTGGGATTACAGATGTGGGCCACCGCACCCAGCCTAGATGT TACCTGCCTCGGCCTCCCAAAATGCTGGGATTGCAGATGTGGGCCACCGCACCCAGCCTAGATGT T C 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,lnc-SOWAHB-5:10 RNACentral:URS0000D5D8AE,RNACentral:URS0000D59968,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,lincRNA exon,exon,intron,intron,intron,intron,intron,intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1230526919 Functional Loss SNV dbSNP153 33..33 33 - - - 17913 RMVar_ID_17913 Human_SNP_ID_190489900 A-to-I Human chr4 + 77042716 77042716 77042716 CCCACCTCAGCCTCCTGAGTAGGTAGGACTATAGACATCAGCAACTATGCCTGGCTAATTTTTTT CCCACCTCAGCCTCCTGAGTAGGTAGGACTATGGACATCAGCAACTATGCCTGGCTAATTTTTTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1001387697 Functional Loss SNV dbSNP153 33..33 33 - - - 17914 RMVar_ID_17914 Human_SNP_ID_190489901 A-to-I Human chr4 + 77042716 77042716 77042716 CCCACCTCAGCCTCCTGAGTAGGTAGGACTATAGACATCAGCAACTATGCCTGGCTAATTTTTTT CCCACCTCAGCCTCCTGAGTAGGTAGGACTATTGACATCAGCAACTATGCCTGGCTAATTTTTTT A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1001387697 Functional Loss SNV dbSNP153 33..33 33 - - - 17915 RMVar_ID_17915 Human_SNP_ID_190494260 A-to-I Human chr4 - 77058527 77058527 77058527 AAACATTTGCTCTGGCTAGCAGTCTTTTGGATAGGTTTTTAGCTACCGTAAAGGTAAGTGTTTTA AAACATTTGCTCTGGCTAGCAGTCTTTTGGATTGGTTTTTAGCTACCGTAAAGGTAAGTGTTTTA T A CCNI Ensembl:ENSG00000118816 Protein coding CDS GSE38233;GSE56152;GSE112787 cultured B-cells;embryonic stem cells,wild type;293 Flip-In T-REx cells,empty vector - 24183664,25708366,29967493 RNA-Seq:(High) rs4595 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_624756,Human_RBP_ID_1981185,Human_RBP_ID_4795479,Human_RBP_ID_5394827,Human_RBP_ID_7329105,Human_RBP_ID_9163084,Human_RBP_ID_9349406,Human_RBP_ID_15204161,Human_RBP_ID_18349391,Human_RBP_ID_19121679,Human_RBP_ID_22826497,Human_RBP_ID_26518128,Human_RBP_ID_27509508,Human_RBP_ID_27730179 Human_Splice_Rec_571761,Human_Splice_Rec_571785,Human_Splice_Rec_571791 RMVar_hsa_circ_320239,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_226750,RMVar_hsa_circ_226754,RMVar_hsa_circ_295656,RMVar_hsa_circ_316696,RMVar_hsa_circ_226753,RMVar_hsa_circ_109366,RMVar_hsa_circ_308793,RMVar_hsa_circ_226755,RMVar_hsa_circ_270560 17916 RMVar_ID_17916 Human_SNP_ID_190494261 A-to-I Human chr4 - 77058527 77058527 77058527 AAACATTTGCTCTGGCTAGCAGTCTTTTGGATAGGTTTTTAGCTACCGTAAAGGTAAGTGTTTTA AAACATTTGCTCTGGCTAGCAGTCTTTTGGATGGGTTTTTAGCTACCGTAAAGGTAAGTGTTTTA T C CCNI Ensembl:ENSG00000118816 Protein coding CDS GSE38233;GSE56152;GSE112787 cultured B-cells;embryonic stem cells,wild type;293 Flip-In T-REx cells,empty vector - 24183664,25708366,29967493 RNA-Seq:(High) rs4595 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_624756,Human_RBP_ID_1981185,Human_RBP_ID_4795479,Human_RBP_ID_5394827,Human_RBP_ID_7329105,Human_RBP_ID_9163084,Human_RBP_ID_9349406,Human_RBP_ID_15204161,Human_RBP_ID_18349391,Human_RBP_ID_19121679,Human_RBP_ID_22826497,Human_RBP_ID_26518128,Human_RBP_ID_27509508,Human_RBP_ID_27730179 Human_Splice_Rec_571761,Human_Splice_Rec_571785,Human_Splice_Rec_571791 RMVar_hsa_circ_320239,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_226750,RMVar_hsa_circ_226754,RMVar_hsa_circ_295656,RMVar_hsa_circ_316696,RMVar_hsa_circ_226753,RMVar_hsa_circ_109366,RMVar_hsa_circ_308793,RMVar_hsa_circ_226755,RMVar_hsa_circ_270560 17917 RMVar_ID_17917 Human_SNP_ID_190494842 A-to-I Human chr4 - 77060762 77060762 77060762 AAATTAGCCAGGCGTGATGGCACAAGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGGAGA AAATTAGCCAGGCGTGATGGCACAAGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGGAGA T C CCNI Ensembl:ENSG00000118816 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1419827678 Functional Loss SNV dbSNP153 33..33 33 - - - 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 17918 RMVar_ID_17918 Human_SNP_ID_190495799 A-to-I Human chr4 - 77064076 77064076 77064076 CACCATACCTGGCTAATTTTTGTATTTTTAGTAGGGACAGGGTTTCACCATGTTGGCCGAGCTGG CACCATACCTGGCTAATTTTTGTATTTTTAGTGGGGACAGGGTTTCACCATGTTGGCCGAGCTGG T C CCNI Ensembl:ENSG00000118816 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1286094106 Functional Loss SNV dbSNP153 33..33 33 - - - 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 17919 RMVar_ID_17919 Human_SNP_ID_190496120 A-to-I Human chr4 - 77064776 77064776 77064776 ACTTGGGAGGCTGAGGTATGAGAATTGCTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCCGAGAT ACTTGGGAGGCTGAGGTATGAGAATTGCTTGATCCCAGGAGGCAGAGGTTGCAGTGAGCCGAGAT T A CCNI Ensembl:ENSG00000118816 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1459734515 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_571789 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 17920 RMVar_ID_17920 Human_SNP_ID_190496148 A-to-I Human chr4 - 77064867 77064867 77064867 GAGACCAGCCATGGTCAACATGGCGAAACCCCATCTCTACTAAAAATACAAAAATTAGCTGGGTG GAGACCAGCCATGGTCAACATGGCGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCTGGGTG T C CCNI Ensembl:ENSG00000118816 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs573665094 Functional Loss SNV dbSNP153 33..33 33 - - - 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 17921 RMVar_ID_17921 Human_SNP_ID_190496149 A-to-I Human chr4 - 77064867 77064867 77064867 GAGACCAGCCATGGTCAACATGGCGAAACCCCATCTCTACTAAAAATACAAAAATTAGCTGGGTG GAGACCAGCCATGGTCAACATGGCGAAACCCCCTCTCTACTAAAAATACAAAAATTAGCTGGGTG T G CCNI Ensembl:ENSG00000118816 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs573665094 Functional Loss SNV dbSNP153 33..33 33 - - - 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 17922 RMVar_ID_17922 Human_SNP_ID_190496456 A-to-I Human chr4 - 77066014 77066014 77066014 TCACTGCAACCCCTGCCTCCCGGGCTCAAGCAATCCTCTCACCTCAGCCTCCTGAGTAGCTGGGA TCACTGCAACCCCTGCCTCCCGGGCTCAAGCAGTCCTCTCACCTCAGCCTCCTGAGTAGCTGGGA T C CCNI Ensembl:ENSG00000118816 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs538589793 Functional Loss SNV dbSNP153 33..33 33 - - - 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 17923 RMVar_ID_17923 Human_SNP_ID_190711820 A-to-I Human chr4 + 77887574 77887574 77887574 TTGAGACAAGGTCTCTCTCTGTTGTCCAGACTAGAAGATGGTGGTGCAATTATGGCTCACTGCAG TTGAGACAAGGTCTCTCTCTGTTGTCCAGACTGGAAGATGGTGGTGCAATTATGGCTCACTGCAG A G MRPL1 Ensembl:ENSG00000169288 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1226777097 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24065515 RMVar_hsa_circ_292404,RMVar_hsa_circ_322184,RMVar_hsa_circ_48329,RMVar_hsa_circ_319773,RMVar_hsa_circ_226772,RMVar_hsa_circ_306363,RMVar_hsa_circ_226775,RMVar_hsa_circ_16618,RMVar_hsa_circ_82893,RMVar_hsa_circ_226776 17924 RMVar_ID_17924 Human_SNP_ID_190782456 A-to-I Human chr4 - 78180916 78180916 78180916 CAAACCGTGGCAGCAGGACCGACAAGTCAAGTACTTCTGCTCCTGATGTGGATGACCCAGAGGCA CAAACCGTGGCAGCAGGACCGACAAGTCAAGTGCTTCTGCTCCTGATGTGGATGACCCAGAGGCA T C SERBP1P5 Ensembl:ENSG00000249565 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879226484 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5607764,Human_RBP_ID_9165583 17925 RMVar_ID_17925 Human_SNP_ID_190934679 A-to-I Human chr4 + 78806378 78806378 78806378 AAAATTTTTTTTTGTAGAGGTAGAGTCTTGCTATGTTGTGCAGGCTGGCCTTGAACTCCTGGCTT AAAATTTTTTTTTGTAGAGGTAGAGTCTTGCTGTGTTGTGCAGGCTGGCCTTGAACTCCTGGCTT A G BMP2K Ensembl:ENSG00000138756 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs922096292 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82516,RMVar_hsa_circ_226887 17926 RMVar_ID_17926 Human_SNP_ID_190961354 A-to-I Human chr4 - 78919479 78919479 78919479 TGCATGTGTTAGCATTGCATTGATAACTCAGAATCTTGATAAACACTTAATATTTGGGCCTGAAG TGCATGTGTTAGCATTGCATTGATAACTCAGAGTCTTGATAAACACTTAATATTTGGGCCTGAAG T C PAQR3 Ensembl:ENSG00000163291 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1487304910 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_625071,Human_RBP_ID_15207258,Human_RBP_ID_18349546 RMVar_hsa_circ_89258,RMVar_hsa_circ_7199,RMVar_hsa_circ_20234,RMVar_hsa_circ_46954,RMVar_hsa_circ_123834,RMVar_hsa_circ_226913,RMVar_hsa_circ_226914 17927 RMVar_ID_17927 Human_SNP_ID_191054818 A-to-I Human chr4 + 79325737 79325737 79325737 GCCAGAACATAGCCCACAATCTTCCCGTCCTCATCCTCAGCGATGTAAGAAAGCTGGGGCCAGGA GCCAGAACATAGCCCACAATCTTCCCGTCCTCGTCCTCAGCGATGTAAGAAAGCTGGGGCCAGGA A G LINC01088 RNACentral:URS00008BC062 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1343022888 Functional Loss SNV dbSNP153 33..33 33 - - - 17928 RMVar_ID_17928 Human_SNP_ID_191195659 A-to-I Human chr4 - 79902115 79902115 79902115 AAATGTCAGTGGGTGATCCAAAATAAATTGTTAAAGTTATTAAAATGTACATTTAAGTAGGTTTC AAATGTCAGTGGGTGATCCAAAATAAATTGTTGAAGTTATTAAAATGTACATTTAAGTAGGTTTC T C ANTXR2 Ensembl:ENSG00000163297 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1239998470 Functional Loss SNV dbSNP153 33..33 33 - - - 17929 RMVar_ID_17929 Human_SNP_ID_191235719 A-to-I Human chr4 - 80080110 80080109 80080110 CCATACTTAATAACCAAGTCTCGGAAAACTAAACCATCACCTGCAATGTTTCCTAGAGCCCATAC CCATACTTAATAACCAAGTCTCGGAAAACTAA_CCATCACCTGCAATGTTTCCTAGAGCCCATAC GT G ANTXR2 Ensembl:ENSG00000163297 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs993508817 Functional Loss DEL dbSNP153 33..33 33 - - - 17930 RMVar_ID_17930 Human_SNP_ID_191366226 A-to-I Human chr4 + 80611983 80611983 80611983 AATTTTCTAATGCTGAACCAGATTAATGAATAAATGCTGTGTGAAATTCACAAATCGTCGATGAT AATTTTCTAATGCTGAACCAGATTAATGAATACATGCTGTGTGAAATTCACAAATCGTCGATGAT A C CFAP299 Ensembl:ENSG00000197826 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs943081757 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_226943 17931 RMVar_ID_17931 Human_SNP_ID_191366227 A-to-I Human chr4 + 80611983 80611983 80611983 AATTTTCTAATGCTGAACCAGATTAATGAATAAATGCTGTGTGAAATTCACAAATCGTCGATGAT AATTTTCTAATGCTGAACCAGATTAATGAATATATGCTGTGTGAAATTCACAAATCGTCGATGAT A T CFAP299 Ensembl:ENSG00000197826 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs943081757 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_226943 17932 RMVar_ID_17932 Human_SNP_ID_191803250 A-to-I Human chr4 - 82424361 82424361 82424361 TTCCCTTCTGGTTATCTGAAGACTGTCCTGAAAGGAAGACATAAGTGTTGTGATTAGTAGAAGCT TTCCCTTCTGGTTATCTGAAGACTGTCCTGAATGGAAGACATAAGTGTTGTGATTAGTAGAAGCT T A HNRNPDL Ensembl:ENSG00000152795 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1390233610 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_625420,Human_RBP_ID_1640760,Human_RBP_ID_1981503,Human_RBP_ID_2860925,Human_RBP_ID_3744449,Human_RBP_ID_7332100,Human_RBP_ID_8595307,Human_RBP_ID_15209268,Human_RBP_ID_18826940,Human_RBP_ID_21069069,Human_RBP_ID_24066519,Human_RBP_ID_27730533 17933 RMVar_ID_17933 Human_SNP_ID_191806002 A-to-I Human chr4 + 82431943 82431939 82431943 AAGGCTTTTTTTTTTTTTTCTTTGAGAGTCTCACTCTGTTCCCAGGCTGGAGTGGAGTGGAGTGG AAGGCTTTTTTTTTTTTTTCTTTGAGAGT____CTCTGTTCCCAGGCTGGAGTGGAGTGGAGTGG TCTCA T ENOPH1 Ensembl:ENSG00000145293 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1488702071 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_15209557 RMVar_hsa_circ_226967,RMVar_hsa_circ_99727 17934 RMVar_ID_17934 Human_SNP_ID_191809944 A-to-I Human chr4 + 82448496 82448496 82448496 ATTGGACAGGCTGGTCTAGAACTCCTGATTTCAAGTGATCTACCCTCCTCGGCCTCCCAAAGTGC ATTGGACAGGCTGGTCTAGAACTCCTGATTTCCAGTGATCTACCCTCCTCGGCCTCCCAAAGTGC A C ENOPH1 Ensembl:ENSG00000145293 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1033522978 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_226967,RMVar_hsa_circ_99727,RMVar_hsa_circ_288423,RMVar_hsa_circ_293650,RMVar_hsa_circ_287100,RMVar_hsa_circ_226968,RMVar_hsa_circ_226969,RMVar_hsa_circ_226970 17935 RMVar_ID_17935 Human_SNP_ID_191812857 A-to-I Human chr4 + 82460264 82460264 82460264 TGCAAGTATGTATATATGTGTATGCTCAGATTAACTTCCATAGGTACATAAGTGAAAGAAGTCTC TGCAAGTATGTATATATGTGTATGCTCAGATTGACTTCCATAGGTACATAAGTGAAAGAAGTCTC A G ENOPH1 Ensembl:ENSG00000145293 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs536861071 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_625537,Human_RBP_ID_17295481,Human_RBP_ID_17525221,Human_RBP_ID_24066615 RMVar_hsa_circ_226973,RMVar_hsa_circ_116487 17936 RMVar_ID_17936 Human_SNP_ID_191898949 A-to-I Human chr4 - 82822825 82822825 82822825 GGAATTACAGGCATGTGCCACCACGCCCGGCTAATTTTGTATTTTTAGAAGAGACAGGGTTTCTC GGAATTACAGGCATGTGCCACCACGCCCGGCTTATTTTGTATTTTTAGAAGAGACAGGGTTTCTC T A SEC31A Ensembl:ENSG00000138674 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1398896941 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_226986,RMVar_hsa_circ_90287,RMVar_hsa_circ_98687,RMVar_hsa_circ_125182,RMVar_hsa_circ_91568,RMVar_hsa_circ_226988,RMVar_hsa_circ_226989,RMVar_hsa_circ_226987,RMVar_hsa_circ_226990,RMVar_hsa_circ_66157,RMVar_hsa_circ_334451,RMVar_hsa_circ_366391,RMVar_hsa_circ_357911,RMVar_hsa_circ_294456,RMVar_hsa_circ_226991 17937 RMVar_ID_17937 Human_SNP_ID_191902982 A-to-I Human chr4 - 82839532 82839532 82839532 CTTGTAATCCTGCCACTTTGGGAGGCCGAGGCAGGTGGATCACCTGAGGTCAGGAGTTGAGACCA CTTGTAATCCTGCCACTTTGGGAGGCCGAGGCTGGTGGATCACCTGAGGTCAGGAGTTGAGACCA T A SEC31A Ensembl:ENSG00000138674 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs946706067 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25823454 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_39618,RMVar_hsa_circ_66854,RMVar_hsa_circ_119957,RMVar_hsa_circ_226996,RMVar_hsa_circ_66529 17938 RMVar_ID_17938 Human_SNP_ID_191907907 A-to-I Human chr4 - 82858178 82858178 82858178 TTGATCTCCTGACCTTGTGATCCGCCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGCACGCA TTGATCTCCTGACCTTGTGATCCGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCACGCA T C SEC31A Ensembl:ENSG00000138674 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1433116426 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22727258 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_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_331988,RMVar_hsa_circ_295836,RMVar_hsa_circ_41586,RMVar_hsa_circ_226998,RMVar_hsa_circ_226997,RMVar_hsa_circ_227008,RMVar_hsa_circ_120871,RMVar_hsa_circ_309134,RMVar_hsa_circ_350923,RMVar_hsa_circ_226999,RMVar_hsa_circ_367722,RMVar_hsa_circ_22264,RMVar_hsa_circ_227002,RMVar_hsa_circ_227003,RMVar_hsa_circ_227005,RMVar_hsa_circ_119465,RMVar_hsa_circ_327749,RMVar_hsa_circ_287866,RMVar_hsa_circ_227006,RMVar_hsa_circ_227004,RMVar_hsa_circ_118538,RMVar_hsa_circ_320683,RMVar_hsa_circ_370517,RMVar_hsa_circ_374948,RMVar_hsa_circ_297624,RMVar_hsa_circ_227010,RMVar_hsa_circ_227011,RMVar_hsa_circ_227009,RMVar_hsa_circ_4603,RMVar_hsa_circ_69666,RMVar_hsa_circ_353898,RMVar_hsa_circ_265470,RMVar_hsa_circ_288793,RMVar_hsa_circ_74473,RMVar_hsa_circ_227014,RMVar_hsa_circ_3876,RMVar_hsa_circ_319636,RMVar_hsa_circ_321587,RMVar_hsa_circ_369488,RMVar_hsa_circ_310758,RMVar_hsa_circ_227016,RMVar_hsa_circ_57386,RMVar_hsa_circ_227017,RMVar_hsa_circ_321663,RMVar_hsa_circ_227015 17939 RMVar_ID_17939 Human_SNP_ID_191908551 A-to-I Human chr4 - 82860252 82860252 82860252 GTTTAAGGAGGTAAAATCTTCCCCTTTGTCTCAATGAGCTATTTGTTTCATAGTAGCTTACACAT GTTTAAGGAGGTAAAATCTTCCCCTTTGTCTCGATGAGCTATTTGTTTCATAGTAGCTTACACAT T C SEC31A Ensembl:ENSG00000138674 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4693520 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_331988,RMVar_hsa_circ_295836,RMVar_hsa_circ_41586,RMVar_hsa_circ_226998,RMVar_hsa_circ_226997,RMVar_hsa_circ_227008,RMVar_hsa_circ_120871,RMVar_hsa_circ_309134,RMVar_hsa_circ_350923,RMVar_hsa_circ_226999,RMVar_hsa_circ_367722,RMVar_hsa_circ_22264,RMVar_hsa_circ_227002,RMVar_hsa_circ_227003,RMVar_hsa_circ_227005,RMVar_hsa_circ_119465,RMVar_hsa_circ_327749,RMVar_hsa_circ_287866,RMVar_hsa_circ_227006,RMVar_hsa_circ_227004,RMVar_hsa_circ_118538,RMVar_hsa_circ_320683,RMVar_hsa_circ_370517,RMVar_hsa_circ_374948,RMVar_hsa_circ_297624,RMVar_hsa_circ_227010,RMVar_hsa_circ_227011,RMVar_hsa_circ_227009,RMVar_hsa_circ_4603,RMVar_hsa_circ_69666,RMVar_hsa_circ_353898,RMVar_hsa_circ_265470,RMVar_hsa_circ_288793,RMVar_hsa_circ_74473,RMVar_hsa_circ_227014,RMVar_hsa_circ_3876,RMVar_hsa_circ_319636,RMVar_hsa_circ_321587,RMVar_hsa_circ_369488,RMVar_hsa_circ_310758,RMVar_hsa_circ_227016,RMVar_hsa_circ_57386,RMVar_hsa_circ_227017,RMVar_hsa_circ_321663,RMVar_hsa_circ_227015 17940 RMVar_ID_17940 Human_SNP_ID_191909326 A-to-I Human chr4 - 82863396 82863396 82863396 GGTCTTTGTTTTAAGAATATGTCTTTTTTTTTAAAGGTAAACTTTGAGGATGATTCTCGTGGAAA GGTCTTTGTTTTAAGAATATGTCTTTTTTTTTTAAGGTAAACTTTGAGGATGATTCTCGTGGAAA T A SEC31A Ensembl:ENSG00000138674 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs927953902 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_71440,Human_RBP_ID_15211268 Human_Splice_Rec_574203,Human_Splice_Rec_574269,Human_Splice_Rec_574317,Human_Splice_Rec_574361,Human_Splice_Rec_574413,Human_Splice_Rec_574463,Human_Splice_Rec_574513,Human_Splice_Rec_574563,Human_Splice_Rec_574615,Human_Splice_Rec_574661,Human_Splice_Rec_574717,Human_Splice_Rec_574761,Human_Splice_Rec_574813,Human_Splice_Rec_574881,Human_Splice_Rec_574903,Human_Splice_Rec_574919,Human_Splice_Rec_574931 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_20979,RMVar_hsa_circ_66854,RMVar_hsa_circ_119957,RMVar_hsa_circ_226996,RMVar_hsa_circ_66529,RMVar_hsa_circ_99033,RMVar_hsa_circ_331988,RMVar_hsa_circ_41586,RMVar_hsa_circ_226998,RMVar_hsa_circ_227008,RMVar_hsa_circ_120871,RMVar_hsa_circ_309134,RMVar_hsa_circ_350923,RMVar_hsa_circ_226999,RMVar_hsa_circ_367722,RMVar_hsa_circ_22264,RMVar_hsa_circ_227002,RMVar_hsa_circ_227003,RMVar_hsa_circ_227005,RMVar_hsa_circ_119465,RMVar_hsa_circ_327749,RMVar_hsa_circ_287866,RMVar_hsa_circ_227006,RMVar_hsa_circ_227004,RMVar_hsa_circ_118538,RMVar_hsa_circ_370517,RMVar_hsa_circ_374948,RMVar_hsa_circ_297624,RMVar_hsa_circ_227010,RMVar_hsa_circ_227011,RMVar_hsa_circ_227009,RMVar_hsa_circ_69666,RMVar_hsa_circ_353898,RMVar_hsa_circ_265470,RMVar_hsa_circ_74473,RMVar_hsa_circ_3876,RMVar_hsa_circ_319636,RMVar_hsa_circ_369488,RMVar_hsa_circ_310758,RMVar_hsa_circ_227016,RMVar_hsa_circ_57386,RMVar_hsa_circ_33499,RMVar_hsa_circ_321663,RMVar_hsa_circ_227015,RMVar_hsa_circ_323349,RMVar_hsa_circ_14613,RMVar_hsa_circ_18797,RMVar_hsa_circ_227020,RMVar_hsa_circ_227019,RMVar_hsa_circ_356828,RMVar_hsa_circ_64636,RMVar_hsa_circ_350914,RMVar_hsa_circ_227021 17941 RMVar_ID_17941 Human_SNP_ID_191909327 A-to-I Human chr4 - 82863396 82863396 82863396 GGTCTTTGTTTTAAGAATATGTCTTTTTTTTTAAAGGTAAACTTTGAGGATGATTCTCGTGGAAA GGTCTTTGTTTTAAGAATATGTCTTTTTTTTTGAAGGTAAACTTTGAGGATGATTCTCGTGGAAA T C SEC31A Ensembl:ENSG00000138674 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs927953902 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_71440,Human_RBP_ID_15211268 Human_Splice_Rec_574203,Human_Splice_Rec_574269,Human_Splice_Rec_574317,Human_Splice_Rec_574361,Human_Splice_Rec_574413,Human_Splice_Rec_574463,Human_Splice_Rec_574513,Human_Splice_Rec_574563,Human_Splice_Rec_574615,Human_Splice_Rec_574661,Human_Splice_Rec_574717,Human_Splice_Rec_574761,Human_Splice_Rec_574813,Human_Splice_Rec_574881,Human_Splice_Rec_574903,Human_Splice_Rec_574919,Human_Splice_Rec_574931 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_20979,RMVar_hsa_circ_66854,RMVar_hsa_circ_119957,RMVar_hsa_circ_226996,RMVar_hsa_circ_66529,RMVar_hsa_circ_99033,RMVar_hsa_circ_331988,RMVar_hsa_circ_41586,RMVar_hsa_circ_226998,RMVar_hsa_circ_227008,RMVar_hsa_circ_120871,RMVar_hsa_circ_309134,RMVar_hsa_circ_350923,RMVar_hsa_circ_226999,RMVar_hsa_circ_367722,RMVar_hsa_circ_22264,RMVar_hsa_circ_227002,RMVar_hsa_circ_227003,RMVar_hsa_circ_227005,RMVar_hsa_circ_119465,RMVar_hsa_circ_327749,RMVar_hsa_circ_287866,RMVar_hsa_circ_227006,RMVar_hsa_circ_227004,RMVar_hsa_circ_118538,RMVar_hsa_circ_370517,RMVar_hsa_circ_374948,RMVar_hsa_circ_297624,RMVar_hsa_circ_227010,RMVar_hsa_circ_227011,RMVar_hsa_circ_227009,RMVar_hsa_circ_69666,RMVar_hsa_circ_353898,RMVar_hsa_circ_265470,RMVar_hsa_circ_74473,RMVar_hsa_circ_3876,RMVar_hsa_circ_319636,RMVar_hsa_circ_369488,RMVar_hsa_circ_310758,RMVar_hsa_circ_227016,RMVar_hsa_circ_57386,RMVar_hsa_circ_33499,RMVar_hsa_circ_321663,RMVar_hsa_circ_227015,RMVar_hsa_circ_323349,RMVar_hsa_circ_14613,RMVar_hsa_circ_18797,RMVar_hsa_circ_227020,RMVar_hsa_circ_227019,RMVar_hsa_circ_356828,RMVar_hsa_circ_64636,RMVar_hsa_circ_350914,RMVar_hsa_circ_227021 17942 RMVar_ID_17942 Human_SNP_ID_191910609 A-to-I Human chr4 - 82868316 82868316 82868316 TTTGTATTTTTTTGTAGAGATGGGGTTTTGCCATGTTCCCCATGCTGGTCTTGAACTCCTGGGCT TTTGTATTTTTTTGTAGAGATGGGGTTTTGCCGTGTTCCCCATGCTGGTCTTGAACTCCTGGGCT T C SEC31A Ensembl:ENSG00000138674 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1022445747 Functional Loss SNV dbSNP153 33..33 33 - - - 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_20979,RMVar_hsa_circ_66854,RMVar_hsa_circ_66529,RMVar_hsa_circ_99033,RMVar_hsa_circ_331988,RMVar_hsa_circ_41586,RMVar_hsa_circ_226998,RMVar_hsa_circ_309134,RMVar_hsa_circ_350923,RMVar_hsa_circ_226999,RMVar_hsa_circ_367722,RMVar_hsa_circ_22264,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_297624,RMVar_hsa_circ_227010,RMVar_hsa_circ_227011,RMVar_hsa_circ_227009,RMVar_hsa_circ_69666,RMVar_hsa_circ_353898,RMVar_hsa_circ_3876,RMVar_hsa_circ_319636,RMVar_hsa_circ_369488,RMVar_hsa_circ_310758,RMVar_hsa_circ_227016,RMVar_hsa_circ_33499,RMVar_hsa_circ_321663,RMVar_hsa_circ_227015,RMVar_hsa_circ_323349,RMVar_hsa_circ_14613,RMVar_hsa_circ_25009,RMVar_hsa_circ_34907,RMVar_hsa_circ_18797,RMVar_hsa_circ_227020,RMVar_hsa_circ_227019,RMVar_hsa_circ_356828,RMVar_hsa_circ_64636,RMVar_hsa_circ_350914,RMVar_hsa_circ_227021,RMVar_hsa_circ_227025,RMVar_hsa_circ_319782,RMVar_hsa_circ_331913,RMVar_hsa_circ_367274,RMVar_hsa_circ_331490,RMVar_hsa_circ_296356,RMVar_hsa_circ_227026,RMVar_hsa_circ_227024,RMVar_hsa_circ_94343,RMVar_hsa_circ_227027 17943 RMVar_ID_17943 Human_SNP_ID_191910629 A-to-I Human chr4 - 82868388 82868388 82868388 CCATCAGTCCTCCCACCTCAGCCTCCCAGCTAACAGGGACTACAGGCGTGCAGCACCGTGCCTGG CCATCAGTCCTCCCACCTCAGCCTCCCAGCTAGCAGGGACTACAGGCGTGCAGCACCGTGCCTGG T C SEC31A Ensembl:ENSG00000138674 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4693523 Functional Loss SNV dbSNP153 33..33 33 - - - 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_20979,RMVar_hsa_circ_66854,RMVar_hsa_circ_66529,RMVar_hsa_circ_99033,RMVar_hsa_circ_331988,RMVar_hsa_circ_41586,RMVar_hsa_circ_226998,RMVar_hsa_circ_309134,RMVar_hsa_circ_350923,RMVar_hsa_circ_226999,RMVar_hsa_circ_367722,RMVar_hsa_circ_22264,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_297624,RMVar_hsa_circ_227010,RMVar_hsa_circ_227011,RMVar_hsa_circ_227009,RMVar_hsa_circ_69666,RMVar_hsa_circ_353898,RMVar_hsa_circ_3876,RMVar_hsa_circ_319636,RMVar_hsa_circ_369488,RMVar_hsa_circ_310758,RMVar_hsa_circ_227016,RMVar_hsa_circ_33499,RMVar_hsa_circ_321663,RMVar_hsa_circ_227015,RMVar_hsa_circ_323349,RMVar_hsa_circ_14613,RMVar_hsa_circ_25009,RMVar_hsa_circ_34907,RMVar_hsa_circ_18797,RMVar_hsa_circ_227020,RMVar_hsa_circ_227019,RMVar_hsa_circ_356828,RMVar_hsa_circ_64636,RMVar_hsa_circ_350914,RMVar_hsa_circ_227021,RMVar_hsa_circ_227025,RMVar_hsa_circ_319782,RMVar_hsa_circ_331913,RMVar_hsa_circ_367274,RMVar_hsa_circ_331490,RMVar_hsa_circ_296356,RMVar_hsa_circ_227026,RMVar_hsa_circ_227024,RMVar_hsa_circ_94343,RMVar_hsa_circ_227027 17944 RMVar_ID_17944 Human_SNP_ID_191910729 A-to-I Human chr4 - 82868771 82868771 82868771 GGATCGCTTGAGCCCAGGAGGTCAAGACTCCAATGAGCTGTGATTGCGCCACTGCACTCCAGCCT GGATCGCTTGAGCCCAGGAGGTCAAGACTCCAGTGAGCTGTGATTGCGCCACTGCACTCCAGCCT T C SEC31A Ensembl:ENSG00000138674 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs539709601 Functional Loss SNV dbSNP153 33..33 33 - - - 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_20979,RMVar_hsa_circ_66854,RMVar_hsa_circ_66529,RMVar_hsa_circ_99033,RMVar_hsa_circ_331988,RMVar_hsa_circ_41586,RMVar_hsa_circ_226998,RMVar_hsa_circ_309134,RMVar_hsa_circ_350923,RMVar_hsa_circ_226999,RMVar_hsa_circ_367722,RMVar_hsa_circ_22264,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_297624,RMVar_hsa_circ_227010,RMVar_hsa_circ_227011,RMVar_hsa_circ_227009,RMVar_hsa_circ_69666,RMVar_hsa_circ_353898,RMVar_hsa_circ_3876,RMVar_hsa_circ_319636,RMVar_hsa_circ_369488,RMVar_hsa_circ_310758,RMVar_hsa_circ_227016,RMVar_hsa_circ_33499,RMVar_hsa_circ_321663,RMVar_hsa_circ_227015,RMVar_hsa_circ_323349,RMVar_hsa_circ_14613,RMVar_hsa_circ_25009,RMVar_hsa_circ_34907,RMVar_hsa_circ_18797,RMVar_hsa_circ_227020,RMVar_hsa_circ_227019,RMVar_hsa_circ_356828,RMVar_hsa_circ_64636,RMVar_hsa_circ_350914,RMVar_hsa_circ_227021,RMVar_hsa_circ_227025,RMVar_hsa_circ_319782,RMVar_hsa_circ_331913,RMVar_hsa_circ_367274,RMVar_hsa_circ_331490,RMVar_hsa_circ_296356,RMVar_hsa_circ_227026,RMVar_hsa_circ_227024,RMVar_hsa_circ_94343,RMVar_hsa_circ_227027 17945 RMVar_ID_17945 Human_SNP_ID_191911653 A-to-I Human chr4 - 82872314 82872314 82872314 ATGGTGGCTTGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGGATCACTTGAACCTG ATGGTGGCTTGCGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGGATCACTTGAACCTG T C SEC31A Ensembl:ENSG00000138674 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1238978117 Functional Loss SNV dbSNP153 33..33 33 - - - 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_20979,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_226999,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_297624,RMVar_hsa_circ_227010,RMVar_hsa_circ_227011,RMVar_hsa_circ_227009,RMVar_hsa_circ_69666,RMVar_hsa_circ_353898,RMVar_hsa_circ_319636,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_25009,RMVar_hsa_circ_227020,RMVar_hsa_circ_227019,RMVar_hsa_circ_356828,RMVar_hsa_circ_64636,RMVar_hsa_circ_350914,RMVar_hsa_circ_227021,RMVar_hsa_circ_331913,RMVar_hsa_circ_367274,RMVar_hsa_circ_331490,RMVar_hsa_circ_227026,RMVar_hsa_circ_94343,RMVar_hsa_circ_227032,RMVar_hsa_circ_37615,RMVar_hsa_circ_227030,RMVar_hsa_circ_325320,RMVar_hsa_circ_346633,RMVar_hsa_circ_227027,RMVar_hsa_circ_327116,RMVar_hsa_circ_294248,RMVar_hsa_circ_323170,RMVar_hsa_circ_227031,RMVar_hsa_circ_227028,RMVar_hsa_circ_227029,RMVar_hsa_circ_281550,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 17946 RMVar_ID_17946 Human_SNP_ID_191911797 A-to-I Human chr4 - 82872879 82872879 82872879 GCAACATGGTGAAACCCCTTCTCTACTAAAATACAAAAAATTAGCCAGGCATGGTGGTGTGTGCC GCAACATGGTGAAACCCCTTCTCTACTAAAATGCAAAAAATTAGCCAGGCATGGTGGTGTGTGCC T C SEC31A Ensembl:ENSG00000138674 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1359469970 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25823596 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_20979,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_226999,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_297624,RMVar_hsa_circ_227010,RMVar_hsa_circ_227011,RMVar_hsa_circ_227009,RMVar_hsa_circ_69666,RMVar_hsa_circ_353898,RMVar_hsa_circ_319636,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_25009,RMVar_hsa_circ_227020,RMVar_hsa_circ_227019,RMVar_hsa_circ_356828,RMVar_hsa_circ_64636,RMVar_hsa_circ_350914,RMVar_hsa_circ_227021,RMVar_hsa_circ_331913,RMVar_hsa_circ_367274,RMVar_hsa_circ_331490,RMVar_hsa_circ_227026,RMVar_hsa_circ_94343,RMVar_hsa_circ_227032,RMVar_hsa_circ_37615,RMVar_hsa_circ_227030,RMVar_hsa_circ_325320,RMVar_hsa_circ_346633,RMVar_hsa_circ_227027,RMVar_hsa_circ_327116,RMVar_hsa_circ_294248,RMVar_hsa_circ_323170,RMVar_hsa_circ_227031,RMVar_hsa_circ_227028,RMVar_hsa_circ_227029,RMVar_hsa_circ_281550,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 17947 RMVar_ID_17947 Human_SNP_ID_191911902 A-to-I Human chr4 - 82873342 82873338 82873342 TAAGGGTTTTTTTTTTTTTGAGAGGGACTCTCACTCTGTCACCCAGTCTGGAGTGTAGGGGCGCA TAAGGGTTTTTTTTTTTTTGAGAGGGACTCTC____TGTCACCCAGTCTGGAGTGTAGGGGCGCA AGAGT A SEC31A Ensembl:ENSG00000138674 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1248061174 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_2861264 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_20979,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_226999,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_297624,RMVar_hsa_circ_227010,RMVar_hsa_circ_227011,RMVar_hsa_circ_227009,RMVar_hsa_circ_69666,RMVar_hsa_circ_353898,RMVar_hsa_circ_319636,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_25009,RMVar_hsa_circ_227020,RMVar_hsa_circ_227019,RMVar_hsa_circ_356828,RMVar_hsa_circ_64636,RMVar_hsa_circ_350914,RMVar_hsa_circ_227021,RMVar_hsa_circ_331913,RMVar_hsa_circ_367274,RMVar_hsa_circ_331490,RMVar_hsa_circ_227026,RMVar_hsa_circ_94343,RMVar_hsa_circ_227032,RMVar_hsa_circ_37615,RMVar_hsa_circ_227030,RMVar_hsa_circ_325320,RMVar_hsa_circ_346633,RMVar_hsa_circ_227027,RMVar_hsa_circ_327116,RMVar_hsa_circ_294248,RMVar_hsa_circ_323170,RMVar_hsa_circ_227031,RMVar_hsa_circ_227028,RMVar_hsa_circ_227029,RMVar_hsa_circ_281550,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 17948 RMVar_ID_17948 Human_SNP_ID_191912646 A-to-I Human chr4 - 82876382 82876382 82876382 TATCCAGCCAGGTTTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGTGGA TATCCAGCCAGGTTTGGTGGCTCACGCCTGTATTCCCAGCACTTTGGGAGGCCGAGGCAGGTGGA T A SEC31A Ensembl:ENSG00000138674 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1304323385 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_323170,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_227037 17949 RMVar_ID_17949 Human_SNP_ID_191912812 A-to-I Human chr4 - 82877107 82877107 82877107 CTTCTGTCTCAGCCACCTGAGTAGCTGGGACTACAGGCATGAGCCACAACACCTGGCTAATTTTT CTTCTGTCTCAGCCACCTGAGTAGCTGGGACTGCAGGCATGAGCCACAACACCTGGCTAATTTTT T C SEC31A Ensembl:ENSG00000138674 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs572506313 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_323170,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_227037 17950 RMVar_ID_17950 Human_SNP_ID_191912995 A-to-I Human chr4 - 82877848 82877848 82877848 GTCTCTACTAAAAATACAAAAATTAGCCGGGCATGGTGGCAGGCACCTGTAATCCCAGCTATTCG GTCTCTACTAAAAATACAAAAATTAGCCGGGCGTGGTGGCAGGCACCTGTAATCCCAGCTATTCG T C SEC31A Ensembl:ENSG00000138674 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs556809823 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_323170,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_227037 17951 RMVar_ID_17951 Human_SNP_ID_191913012 A-to-I Human chr4 - 82877924 82877924 82877924 GCACTTTGAGAGGCCGAGGCAGACAGATCATGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACGT GCACTTTGAGAGGCCGAGGCAGACAGATCATGCGGTCAGGAGTTCGAGACCAGCCTGGCCAACGT T G SEC31A Ensembl:ENSG00000138674 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs997819393 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_323170,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_227037 17952 RMVar_ID_17952 Human_SNP_ID_191917690 A-to-I Human chr4 - 82895305 82895305 82895305 CCACCACACCCAGCTAATTTTTTTTATTAAGTAGAGACCATGTTTTGCCATGTTGGCCAGACTGG CCACCACACCCAGCTAATTTTTTTTATTAAGTGGAGACCATGTTTTGCCATGTTGGCCAGACTGG T C SEC31A,THAP9-AS1 Ensembl:ENSG00000138674,Ensembl:ENSG00000251022 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1184367859 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15211745,Human_RBP_ID_25836032 RMVar_hsa_circ_90287,RMVar_hsa_circ_226989,RMVar_hsa_circ_95034,RMVar_hsa_circ_227036,RMVar_hsa_circ_104688,RMVar_hsa_circ_227037 17953 RMVar_ID_17953 Human_SNP_ID_191917957 A-to-I Human chr4 - 82896610 82896610 82896610 GAACTGCAGGCGTGTGCCACCACACCTGGCTAATTTTTTGTATTTTTGGTAGAGAAGGGGTTTTG GAACTGCAGGCGTGTGCCACCACACCTGGCTATTTTTTTGTATTTTTGGTAGAGAAGGGGTTTTG T A SEC31A,THAP9-AS1 Ensembl:ENSG00000138674,Ensembl:ENSG00000251022 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277098058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5212411 RMVar_hsa_circ_90287,RMVar_hsa_circ_226989,RMVar_hsa_circ_95034,RMVar_hsa_circ_227036,RMVar_hsa_circ_104688,RMVar_hsa_circ_227037 17954 RMVar_ID_17954 Human_SNP_ID_191917958 A-to-I Human chr4 - 82896610 82896610 82896610 GAACTGCAGGCGTGTGCCACCACACCTGGCTAATTTTTTGTATTTTTGGTAGAGAAGGGGTTTTG GAACTGCAGGCGTGTGCCACCACACCTGGCTAGTTTTTTGTATTTTTGGTAGAGAAGGGGTTTTG T C SEC31A,THAP9-AS1 Ensembl:ENSG00000138674,Ensembl:ENSG00000251022 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277098058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5212411 RMVar_hsa_circ_90287,RMVar_hsa_circ_226989,RMVar_hsa_circ_95034,RMVar_hsa_circ_227036,RMVar_hsa_circ_104688,RMVar_hsa_circ_227037 17955 RMVar_ID_17955 Human_SNP_ID_191918220 A-to-I Human chr4 - 82897725 82897721 82897725 TCATTTTATTTTATTTTTTGAGATGGGGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGCGCA TCATTTTATTTTATTTTTTGAGATGGGGTCTC____TGTCACCCAGGCTGGAGTGCAGTGGCGCA AGAGT A SEC31A,THAP9-AS1 Ensembl:ENSG00000138674,Ensembl:ENSG00000251022 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1427165145 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_160025,Human_RBP_ID_5212169 RMVar_hsa_circ_90287,RMVar_hsa_circ_226989,RMVar_hsa_circ_95034,RMVar_hsa_circ_227036,RMVar_hsa_circ_104688,RMVar_hsa_circ_227037 17956 RMVar_ID_17956 Human_SNP_ID_191918222 A-to-I Human chr4 - 82897725 82897725 82897725 TCATTTTATTTTATTTTTTGAGATGGGGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGCGCA TCATTTTATTTTATTTTTTGAGATGGGGTCTCCCTCTGTCACCCAGGCTGGAGTGCAGTGGCGCA T G SEC31A,THAP9-AS1 Ensembl:ENSG00000138674,Ensembl:ENSG00000251022 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1169976012 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_160025,Human_RBP_ID_5212169 RMVar_hsa_circ_90287,RMVar_hsa_circ_226989,RMVar_hsa_circ_95034,RMVar_hsa_circ_227036,RMVar_hsa_circ_104688,RMVar_hsa_circ_227037 17957 RMVar_ID_17957 Human_SNP_ID_191924480 A-to-I Human chr4 - 82922955 82922955 82922955 CACTTTGGAAGGCTGAGGCGGGTGGATCACTTAAGGTCAGGAGTTCAGACCATCCTGGCCAACAA CACTTTGGAAGGCTGAGGCGGGTGGATCACTTGAGGTCAGGAGTTCAGACCATCCTGGCCAACAA T C LIN54 Ensembl:ENSG00000189308 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941038644 Functional Loss SNV dbSNP153 33..33 33 - - - 17958 RMVar_ID_17958 Human_SNP_ID_191924481 A-to-I Human chr4 - 82922955 82922955 82922955 CACTTTGGAAGGCTGAGGCGGGTGGATCACTTAAGGTCAGGAGTTCAGACCATCCTGGCCAACAA CACTTTGGAAGGCTGAGGCGGGTGGATCACTTCAGGTCAGGAGTTCAGACCATCCTGGCCAACAA T G LIN54 Ensembl:ENSG00000189308 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941038644 Functional Loss SNV dbSNP153 33..33 33 - - - 17959 RMVar_ID_17959 Human_SNP_ID_191926016 A-to-I Human chr4 - 82929684 82929684 82929684 CTCCTGCCTCAGCCTCCTAAGTAGCTGGGATTACAGGCATACACCACGACGCCCAGCTAAATTTA CTCCTGCCTCAGCCTCCTAAGTAGCTGGGATTGCAGGCATACACCACGACGCCCAGCTAAATTTA T C LIN54 Ensembl:ENSG00000189308 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs781361735 Functional Loss SNV dbSNP153 33..33 33 - - - 17960 RMVar_ID_17960 Human_SNP_ID_191943574 A-to-I Human chr4 - 83004592 83004592 83004592 CCCGCTACTCGGGAGGCTGAGGTGGGAGGATCACTTGAGCCCAGGTGTCCGAGGCTGCAGTGAGC CCCGCTACTCGGGAGGCTGAGGTGGGAGGATCTCTTGAGCCCAGGTGTCCGAGGCTGCAGTGAGC T A LIN54 Ensembl:ENSG00000189308 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1217114860 Functional Loss SNV dbSNP153 33..33 33 - - - 17961 RMVar_ID_17961 Human_SNP_ID_191955029 A-to-I Human chr4 + 83050515 83050515 83050515 TTTTCACCATGTTTACTAGGTTTCACCATGTTAGCCAGGTTGGTCTCAAACTCCTGACCTCAAGT TTTTCACCATGTTTACTAGGTTTCACCATGTTGGCCAGGTTGGTCTCAAACTCCTGACCTCAAGT A G COPS4 Ensembl:ENSG00000138663 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903865196 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 17962 RMVar_ID_17962 Human_SNP_ID_191955120 A-to-I Human chr4 + 83051001 83051001 83051001 GCTTATGAGACCAGGTACAGTGGCTCACACCTATGGTCCAAGCACTTTGGGAGGCTGAGGTGGGA GCTTATGAGACCAGGTACAGTGGCTCACACCTGTGGTCCAAGCACTTTGGGAGGCTGAGGTGGGA A G COPS4 Ensembl:ENSG00000138663 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1020369155 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 17963 RMVar_ID_17963 Human_SNP_ID_191955218 A-to-I Human chr4 + 83051302 83051302 83051302 TGGGCCTGGTGATATAGTATGGATATGCATCTATACTCCCAGGTAGTTGGGAAGCTGAGGCGAGA TGGGCCTGGTGATATAGTATGGATATGCATCTGTACTCCCAGGTAGTTGGGAAGCTGAGGCGAGA A G COPS4 Ensembl:ENSG00000138663 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1376515437 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 17964 RMVar_ID_17964 Human_SNP_ID_191966701 A-to-I Human chr4 - 83099830 83099830 83099830 ATCTAATTTTTTTTTTTTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGATGG ATCTAATTTTTTTTTTTTTTTGTATTTTTAGTTGAGATGGGGTTTCACCATGTTGGCCAGGATGG T A PLAC8 Ensembl:ENSG00000145287 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1201075512 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99867,RMVar_hsa_circ_227076 17965 RMVar_ID_17965 Human_SNP_ID_192000495 A-to-I Human chr4 - 83238140 83238140 83238140 CCCCAGAGACTCCACCAAAAAACTGTTAAGATAAACAAATACAGTAAAGTTGTAGGATCCAAAAT CCCCAGAGACTCCACCAAAAAACTGTTAAGATTAACAAATACAGTAAAGTTGTAGGATCCAAAAT T A AC114781.2 Ensembl:ENSG00000250057 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991996140 Functional Loss SNV dbSNP153 33..33 33 - - - 17966 RMVar_ID_17966 Human_SNP_ID_192007025 A-to-I Human chr4 - 83265335 83265335 83265335 AAACTCTTGGCCTTAAGTGATCCGCCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAG AAACTCTTGGCCTTAAGTGATCCGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAG T C COQ2 Ensembl:ENSG00000173085 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903395466 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76538,RMVar_hsa_circ_227078,RMVar_hsa_circ_227077,RMVar_hsa_circ_366570,RMVar_hsa_circ_227079 17967 RMVar_ID_17967 Human_SNP_ID_192013783 A-to-I Human chr4 - 83294265 83294265 83294265 CTGACGTGAGGAATTTGATACCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAAATAC CTGACGTGAGGAATTTGATACCAGCCTGGCCACCATGGTGAAACCCCATCTCTACTAAAAAATAC T G HPSE Ensembl:ENSG00000173083 Protein coding 3'UTR GSE47997;GSE126723:GSM3611827,GSM3611828,GSM3611829 K562 cells&HepG2 cells;Bronchiolar epithelium,BEP2D cell line - 23474544,31158229 RNA-Seq:(High) rs771669747 Functional Loss SNV dbSNP153 33..33 33 - - - 17968 RMVar_ID_17968 Human_SNP_ID_192013844 A-to-I Human chr4 - 83294570 83294570 83294570 AATTTTTTGTAGAGATGGGGTCTCGCTATGTTACCCAAACTGGTCCTGAACTCCTGGACTCAATT AATTTTTTGTAGAGATGGGGTCTCGCTATGTTCCCCAAACTGGTCCTGAACTCCTGGACTCAATT T G HPSE Ensembl:ENSG00000173083 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1413655112 Functional Loss SNV dbSNP153 33..33 33 - - - 17969 RMVar_ID_17969 Human_SNP_ID_192013864 A-to-I Human chr4 - 83294644 83294644 83294644 AGTCATCCTCCTGCTTAGCCTCCCAAGTAGCTAGGACCACAGACACATGCCATCACACTTGGCTA AGTCATCCTCCTGCTTAGCCTCCCAAGTAGCTCGGACCACAGACACATGCCATCACACTTGGCTA T G HPSE Ensembl:ENSG00000173083 Protein coding 3'UTR GSE47997;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,29129909,31158229,32596459 RNA-Seq:(High) rs1263038288 Functional Loss SNV dbSNP153 33..33 33 - - - 17970 RMVar_ID_17970 Human_SNP_ID_192013873 A-to-I Human chr4 - 83294698 83294698 83294698 TTGAGTGCAGTGGTGCAATCATAGATCACTGCAGCCTTTTAACTCCTGGGCTCAAGTCATCCTCC TTGAGTGCAGTGGTGCAATCATAGATCACTGCCGCCTTTTAACTCCTGGGCTCAAGTCATCCTCC T G HPSE Ensembl:ENSG00000173083 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1292739698 Functional Loss SNV dbSNP153 33..33 33 - - - 17971 RMVar_ID_17971 Human_SNP_ID_192042839 A-to-I Human chr4 - 83412608 83412607 83412608 TTGCCCAGGCTGGTCTTGAACTCCGGGCCTCAAGCAATCCTTCCATCTTGGCTTCCCAAAGTGTT TTGCCCAGGCTGGTCTTGAACTCCGGGCCTCA_GCAATCCTTCCATCTTGGCTTCCCAAAGTGTT CT C HELQ Ensembl:ENSG00000163312 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs748138799 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5210509 17972 RMVar_ID_17972 Human_SNP_ID_192049006 A-to-I Human chr4 - 83438558 83438558 83438558 TTTTGTAATTTTCATGGAGATAGTATTTCACCATGTTGCCCAGGCTGGTTTCGAACTCCTGAGCT TTTTGTAATTTTCATGGAGATAGTATTTCACCGTGTTGCCCAGGCTGGTTTCGAACTCCTGAGCT T C HELQ Ensembl:ENSG00000163312 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1444238173 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_365021,RMVar_hsa_circ_357011,RMVar_hsa_circ_299869,RMVar_hsa_circ_45128,RMVar_hsa_circ_48165,RMVar_hsa_circ_51978,RMVar_hsa_circ_362882,RMVar_hsa_circ_227084,RMVar_hsa_circ_227085,RMVar_hsa_circ_368358,RMVar_hsa_circ_377199,RMVar_hsa_circ_64778,RMVar_hsa_circ_336482,RMVar_hsa_circ_358595,RMVar_hsa_circ_227090,RMVar_hsa_circ_372507,RMVar_hsa_circ_336843,RMVar_hsa_circ_63853,RMVar_hsa_circ_227091,RMVar_hsa_circ_367883,RMVar_hsa_circ_362001,RMVar_hsa_circ_364365,RMVar_hsa_circ_60982,RMVar_hsa_circ_305381,RMVar_hsa_circ_227092,RMVar_hsa_circ_46996,RMVar_hsa_circ_354247,RMVar_hsa_circ_277379,RMVar_hsa_circ_287790,RMVar_hsa_circ_227094,RMVar_hsa_circ_227096,RMVar_hsa_circ_30100,RMVar_hsa_circ_227095,RMVar_hsa_circ_369157,RMVar_hsa_circ_357894,RMVar_hsa_circ_338397,RMVar_hsa_circ_283783,RMVar_hsa_circ_71938,RMVar_hsa_circ_369158 17973 RMVar_ID_17973 Human_SNP_ID_192049267 A-to-I Human chr4 - 83439504 83439504 83439504 ATACAAAAAATTAGCTGGGTGTGGTGCCTTGCACCTATAATCCCAGCTACTGGGGAGGCTGAGAC ATACAAAAAATTAGCTGGGTGTGGTGCCTTGCCCCTATAATCCCAGCTACTGGGGAGGCTGAGAC T G HELQ Ensembl:ENSG00000163312 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1185162666 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_365021,RMVar_hsa_circ_357011,RMVar_hsa_circ_299869,RMVar_hsa_circ_45128,RMVar_hsa_circ_48165,RMVar_hsa_circ_51978,RMVar_hsa_circ_362882,RMVar_hsa_circ_227084,RMVar_hsa_circ_227085,RMVar_hsa_circ_368358,RMVar_hsa_circ_377199,RMVar_hsa_circ_64778,RMVar_hsa_circ_336482,RMVar_hsa_circ_358595,RMVar_hsa_circ_227090,RMVar_hsa_circ_372507,RMVar_hsa_circ_336843,RMVar_hsa_circ_63853,RMVar_hsa_circ_227091,RMVar_hsa_circ_367883,RMVar_hsa_circ_362001,RMVar_hsa_circ_364365,RMVar_hsa_circ_60982,RMVar_hsa_circ_305381,RMVar_hsa_circ_227092,RMVar_hsa_circ_46996,RMVar_hsa_circ_354247,RMVar_hsa_circ_277379,RMVar_hsa_circ_287790,RMVar_hsa_circ_227094,RMVar_hsa_circ_227096,RMVar_hsa_circ_30100,RMVar_hsa_circ_227095,RMVar_hsa_circ_369157,RMVar_hsa_circ_357894,RMVar_hsa_circ_338397,RMVar_hsa_circ_283783,RMVar_hsa_circ_71938,RMVar_hsa_circ_369158 17974 RMVar_ID_17974 Human_SNP_ID_192054948 A-to-I Human chr4 + 83460219 83460219 83460219 TCTCACTGTCACCCAGGCTGGAGTGCTGTGGCACAATCTCGGCTCACTGCAACCTCTGCCTCCTG TCTCACTGTCACCCAGGCTGGAGTGCTGTGGCGCAATCTCGGCTCACTGCAACCTCTGCCTCCTG A G MRPS18C Ensembl:ENSG00000163319 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1248578342 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_62350 17975 RMVar_ID_17975 Human_SNP_ID_192353002 A-to-I Human chr4 - 84714700 84714700 84714700 GTGATCTGCCCACCTCGGCCTCCCAAAGTGCTAGGATTACAGGCGTGAGCCACCCACCGTGCCCG GTGATCTGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCCACCGTGCCCG T C WDFY3 Ensembl:ENSG00000163625 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1022591850 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4329,RMVar_hsa_circ_68076,RMVar_hsa_circ_266598,RMVar_hsa_circ_227122,RMVar_hsa_circ_81079,RMVar_hsa_circ_110416,RMVar_hsa_circ_376554,RMVar_hsa_circ_299787,RMVar_hsa_circ_227125,RMVar_hsa_circ_227126,RMVar_hsa_circ_316335,RMVar_hsa_circ_5284,RMVar_hsa_circ_13554,RMVar_hsa_circ_52512,RMVar_hsa_circ_77079,RMVar_hsa_circ_227128,RMVar_hsa_circ_227129,RMVar_hsa_circ_36159,RMVar_hsa_circ_42010,RMVar_hsa_circ_374990,RMVar_hsa_circ_80067,RMVar_hsa_circ_126709,RMVar_hsa_circ_227134,RMVar_hsa_circ_7409,RMVar_hsa_circ_12559,RMVar_hsa_circ_227136,RMVar_hsa_circ_227137,RMVar_hsa_circ_227135,RMVar_hsa_circ_227138,RMVar_hsa_circ_90327,RMVar_hsa_circ_281471,RMVar_hsa_circ_319313,RMVar_hsa_circ_120882,RMVar_hsa_circ_273680,RMVar_hsa_circ_113532,RMVar_hsa_circ_23089,RMVar_hsa_circ_78499,RMVar_hsa_circ_227139,RMVar_hsa_circ_227141,RMVar_hsa_circ_227143,RMVar_hsa_circ_227142,RMVar_hsa_circ_227140,RMVar_hsa_circ_107922,RMVar_hsa_circ_112330,RMVar_hsa_circ_227147,RMVar_hsa_circ_14862,RMVar_hsa_circ_227148,RMVar_hsa_circ_285655,RMVar_hsa_circ_298117,RMVar_hsa_circ_292833,RMVar_hsa_circ_280596,RMVar_hsa_circ_97591,RMVar_hsa_circ_99686,RMVar_hsa_circ_78894,RMVar_hsa_circ_24664,RMVar_hsa_circ_120639,RMVar_hsa_circ_227152,RMVar_hsa_circ_227154,RMVar_hsa_circ_227153,RMVar_hsa_circ_227150,RMVar_hsa_circ_227151,RMVar_hsa_circ_227149,RMVar_hsa_circ_227157,RMVar_hsa_circ_87591,RMVar_hsa_circ_91882,RMVar_hsa_circ_227158,RMVar_hsa_circ_227159,RMVar_hsa_circ_271365,RMVar_hsa_circ_272517,RMVar_hsa_circ_377909,RMVar_hsa_circ_50773,RMVar_hsa_circ_227160,RMVar_hsa_circ_227161 17976 RMVar_ID_17976 Human_SNP_ID_192397636 A-to-I Human chr4 - 84900388 84900388 84900388 GACCCCACCTTTATGAAAAAAATTTAAAAATTAGCTGGTTGTGGTGTTGTGTCTGTAATCCCAGA GACCCCACCTTTATGAAAAAAATTTAAAAATTTGCTGGTTGTGGTGTTGTGTCTGTAATCCCAGA T A WDFY3 Ensembl:ENSG00000163625 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1230920540 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41145,RMVar_hsa_circ_354839,RMVar_hsa_circ_85941,RMVar_hsa_circ_227225,RMVar_hsa_circ_296576,RMVar_hsa_circ_227227,RMVar_hsa_circ_318548,RMVar_hsa_circ_266831,RMVar_hsa_circ_286279,RMVar_hsa_circ_227229,RMVar_hsa_circ_274552,RMVar_hsa_circ_89623,RMVar_hsa_circ_227233,RMVar_hsa_circ_227234,RMVar_hsa_circ_296302,RMVar_hsa_circ_227236,RMVar_hsa_circ_227237 17977 RMVar_ID_17977 Human_SNP_ID_192402868 A-to-I Human chr4 - 84922784 84922784 84922784 ATGGTGGTGCACACCTGTAGTCTCAATTACTCAGAAGGCTGAGGCAGGAGGATCCCTTGAGTCAA ATGGTGGTGCACACCTGTAGTCTCAATTACTCCGAAGGCTGAGGCAGGAGGATCCCTTGAGTCAA T G WDFY3 Ensembl:ENSG00000163625 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1453317274 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41145,RMVar_hsa_circ_354839,RMVar_hsa_circ_227225,RMVar_hsa_circ_296576,RMVar_hsa_circ_227227,RMVar_hsa_circ_318548,RMVar_hsa_circ_266831,RMVar_hsa_circ_286279,RMVar_hsa_circ_227229,RMVar_hsa_circ_274552,RMVar_hsa_circ_227234,RMVar_hsa_circ_296302,RMVar_hsa_circ_227237 17978 RMVar_ID_17978 Human_SNP_ID_192412650 A-to-I Human chr4 - 84964786 84964786 84964786 GGGTCACAGTGGGTCATGCCTGTCATTCCAGCACTTTGGGAGGCCAAGGCTGGGGGATCACTTGA GGGTCACAGTGGGTCATGCCTGTCATTCCAGCGCTTTGGGAGGCCAAGGCTGGGGGATCACTTGA T C WDFY3 Ensembl:ENSG00000163625 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1033784726 Functional Loss SNV dbSNP153 33..33 33 - - - 17979 RMVar_ID_17979 Human_SNP_ID_192564620 A-to-I Human chr4 + 85608757 85608757 85608757 TTTTTTTGTATTTTTAGTAGATACGGGGTTTCACCATGTTGGCCAGACTGGTCTCGAACTCCTGA TTTTTTTGTATTTTTAGTAGATACGGGGTTTCCCCATGTTGGCCAGACTGGTCTCGAACTCCTGA A C ARHGAP24 Ensembl:ENSG00000138639 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs894058922 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28579,RMVar_hsa_circ_320839 17980 RMVar_ID_17980 Human_SNP_ID_192618184 A-to-I Human chr4 + 85835886 85835886 85835886 TTTTGTAGTTTTAGTGGAGACAGGGTTTCACCATGTTGGCCAGACTGGTCTGGAACACCTGAGCT TTTTGTAGTTTTAGTGGAGACAGGGTTTCACCGTGTTGGCCAGACTGGTCTGGAACACCTGAGCT A G ARHGAP24 Ensembl:ENSG00000138639 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1339401870 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28579 17981 RMVar_ID_17981 Human_SNP_ID_192737322 A-to-I Human chr4 - 86344835 86344835 86344835 TTTAAAATTTGCCTTTAGAAATAATGATTTCTAAACTCTACTGGGATTTTCTAACATATCAGGTG TTTAAAATTTGCCTTTAGAAATAATGATTTCTCAACTCTACTGGGATTTTCTAACATATCAGGTG T G MAPK10 Ensembl:ENSG00000109339 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs889034260 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25443,RMVar_hsa_circ_362309,RMVar_hsa_circ_43630,RMVar_hsa_circ_364327,RMVar_hsa_circ_354652 17982 RMVar_ID_17982 Human_SNP_ID_192870841 A-to-I Human chr4 - 86923188 86923188 86923188 CCTCAGGAGGCTGAGGTTAGAGGATAGTTTGAACCTAGGAGGTTGAGGCTGCAGTGAATCATGAT CCTCAGGAGGCTGAGGTTAGAGGATAGTTTGAGCCTAGGAGGTTGAGGCTGCAGTGAATCATGAT T C AC093827.5 Ensembl:ENSG00000285458 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1270677041 Functional Loss SNV dbSNP153 33..33 33 - - - 17983 RMVar_ID_17983 Human_SNP_ID_192870877 A-to-I Human chr4 - 86923350 86923350 86923350 ACAAGGGCTCATGCCTGTAATTCCAGCACTTTAGGAGGCCAAGGTAGGAGGATCACTTGAGCCCA ACAAGGGCTCATGCCTGTAATTCCAGCACTTTGGGAGGCCAAGGTAGGAGGATCACTTGAGCCCA T C AC093827.5 Ensembl:ENSG00000285458 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1348116116 Functional Loss SNV dbSNP153 33..33 33 - - - 17984 RMVar_ID_17984 Human_SNP_ID_192870949 A-to-I Human chr4 - 86923711 86923711 86923711 TTGCCCAGGCTGGAGTGCAATGGTGCGATCTCAGATCACTACAACCTCTGCAGCTCTGGTTCAAA TTGCCCAGGCTGGAGTGCAATGGTGCGATCTCGGATCACTACAACCTCTGCAGCTCTGGTTCAAA T C AC093827.5 Ensembl:ENSG00000285458 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1316594601 Functional Loss SNV dbSNP153 33..33 33 - - - 17985 RMVar_ID_17985 Human_SNP_ID_192870958 A-to-I Human chr4 - 86923750 86923750 86923750 TTTTTTTTTTTTTTTTTTTGAGACAGAGTCTCACTCTTGTTGCCCAGGCTGGAGTGCAATGGTGC TTTTTTTTTTTTTTTTTTTGAGACAGAGTCTCCCTCTTGTTGCCCAGGCTGGAGTGCAATGGTGC T G AC093827.5 Ensembl:ENSG00000285458 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1386342446 Functional Loss SNV dbSNP153 33..33 33 - - - 17986 RMVar_ID_17986 Human_SNP_ID_192871054 A-to-I Human chr4 - 86924181 86924181 86924181 AAAGAAACAACCACATGTGGTGGCATGCGCCTATGGTCACAGATACTTGGGAGGCTTAGGTTGGA AAAGAAACAACCACATGTGGTGGCATGCGCCTGTGGTCACAGATACTTGGGAGGCTTAGGTTGGA T C AC093827.5 Ensembl:ENSG00000285458 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1160831387 Functional Loss SNV dbSNP153 33..33 33 - - - 17987 RMVar_ID_17987 Human_SNP_ID_192871075 A-to-I Human chr4 - 86924252 86924252 86924252 GAGGTTGCAGTGAGCTGAGATCACACCACTGCACTCCAATCTGTGTGACAGAGTGAGACTCTGTT GAGGTTGCAGTGAGCTGAGATCACACCACTGCGCTCCAATCTGTGTGACAGAGTGAGACTCTGTT T C AC093827.5 Ensembl:ENSG00000285458 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1394027250 Functional Loss SNV dbSNP153 33..33 33 - - - 17988 RMVar_ID_17988 Human_SNP_ID_192871096 A-to-I Human chr4 - 86924389 86924389 86924389 CAAAATCAGCCTGGCCAACATGGTGAAACCCCATCTGTACTAAAAATACAAAAAATTAGCCAGGT CAAAATCAGCCTGGCCAACATGGTGAAACCCCGTCTGTACTAAAAATACAAAAAATTAGCCAGGT T C AC093827.5 Ensembl:ENSG00000285458 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1180688620 Functional Loss SNV dbSNP153 33..33 33 - - - 17989 RMVar_ID_17989 Human_SNP_ID_192871136 A-to-I Human chr4 - 86924589 86924589 86924589 CCTATAATGCCAGCACTTTGGGAAGCCAAGGCAGGAGGATCGTTTGAGCCCAGGAGTTCAAGACC CCTATAATGCCAGCACTTTGGGAAGCCAAGGCTGGAGGATCGTTTGAGCCCAGGAGTTCAAGACC T A AC093827.5 Ensembl:ENSG00000285458 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042991381 Functional Loss SNV dbSNP153 33..33 33 - - - 17990 RMVar_ID_17990 Human_SNP_ID_192871137 A-to-I Human chr4 - 86924589 86924589 86924589 CCTATAATGCCAGCACTTTGGGAAGCCAAGGCAGGAGGATCGTTTGAGCCCAGGAGTTCAAGACC CCTATAATGCCAGCACTTTGGGAAGCCAAGGCGGGAGGATCGTTTGAGCCCAGGAGTTCAAGACC T C AC093827.5 Ensembl:ENSG00000285458 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042991381 Functional Loss SNV dbSNP153 33..33 33 - - - 17991 RMVar_ID_17991 Human_SNP_ID_192871146 A-to-I Human chr4 - 86924618 86924618 86924618 ATATCAGAGGCTGGGTGTGGTGGCCCATGCCTATAATGCCAGCACTTTGGGAAGCCAAGGCAGGA ATATCAGAGGCTGGGTGTGGTGGCCCATGCCTGTAATGCCAGCACTTTGGGAAGCCAAGGCAGGA T C AC093827.5 Ensembl:ENSG00000285458 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs996638358 Functional Loss SNV dbSNP153 33..33 33 - - - 17992 RMVar_ID_17992 Human_SNP_ID_192871317 A-to-I Human chr4 - 86925350 86925350 86925350 AGATGTGGTGGTGCATGCCCATAATCCTAGCTACTTGGGAGGCTGAGGCACGAGAATTGCTTGAA AGATGTGGTGGTGCATGCCCATAATCCTAGCTGCTTGGGAGGCTGAGGCACGAGAATTGCTTGAA T C AC093827.4,AC093827.5 Ensembl:ENSG00000284968,Ensembl:ENSG00000285458 lincRNA,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1263384430 Functional Loss SNV dbSNP153 33..33 33 - - - 17993 RMVar_ID_17993 Human_SNP_ID_192871328 A-to-I Human chr4 - 86925395 86925395 86925395 CTGGCAAACACGGCAAAACCCCATCTCAAAATACAAAAATTAGCTAGATGTGGTGGTGCATGCCC CTGGCAAACACGGCAAAACCCCATCTCAAAATGCAAAAATTAGCTAGATGTGGTGGTGCATGCCC T C AC093827.4,AC093827.5 Ensembl:ENSG00000284968,Ensembl:ENSG00000285458 lincRNA,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs918329809 Functional Loss SNV dbSNP153 33..33 33 - - - 17994 RMVar_ID_17994 Human_SNP_ID_192871338 A-to-I Human chr4 - 86925444 86925444 86925444 GGGAGACTAAGGCGGGCAGATCACTTGAGCTCAGGAGTTTGAGACGAGCCTGGCAAACACGGCAA GGGAGACTAAGGCGGGCAGATCACTTGAGCTCGGGAGTTTGAGACGAGCCTGGCAAACACGGCAA T C AC093827.4,AC093827.5 Ensembl:ENSG00000284968,Ensembl:ENSG00000285458 lincRNA,Protein coding exon,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs550492318 Functional Loss SNV dbSNP153 33..33 33 - - - 17995 RMVar_ID_17995 Human_SNP_ID_192871341 A-to-I Human chr4 - 86925459 86925459 86925459 TAATCCCAGCACTTTGGGAGACTAAGGCGGGCAGATCACTTGAGCTCAGGAGTTTGAGACGAGCC TAATCCCAGCACTTTGGGAGACTAAGGCGGGCGGATCACTTGAGCTCAGGAGTTTGAGACGAGCC T C AC093827.4,AC093827.5 Ensembl:ENSG00000284968,Ensembl:ENSG00000285458 lincRNA,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1209924755 Functional Loss SNV dbSNP153 33..33 33 - - - 17996 RMVar_ID_17996 Human_SNP_ID_192871457 A-to-I Human chr4 - 86925962 86925962 86925962 TGAGGCAGGAGAATTGCTTCAATCTGGGAGGCAGAGGTTGCAGTGAGCTGAGATCGTGCCATTGC TGAGGCAGGAGAATTGCTTCAATCTGGGAGGCGGAGGTTGCAGTGAGCTGAGATCGTGCCATTGC T C AC093827.4,AC093827.5 Ensembl:ENSG00000284968,Ensembl:ENSG00000285458 lincRNA,Protein coding exon,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs575858870 Functional Loss SNV dbSNP153 33..33 33 - - - 17997 RMVar_ID_17997 Human_SNP_ID_192871487 A-to-I Human chr4 - 86926145 86926145 86926145 GCCAGGCACGGCGGCTCACGCCTGTAATCCCAACACTTTGGGAGGCCAAGGTGGGCAGATCACCT GCCAGGCACGGCGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGCAGATCACCT T C AC093827.4,AC093827.5 Ensembl:ENSG00000284968,Ensembl:ENSG00000285458 lincRNA,Protein coding exon,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs962579159 Functional Loss SNV dbSNP153 33..33 33 - - - 17998 RMVar_ID_17998 Human_SNP_ID_192872933 A-to-I Human chr4 - 86932308 86932308 86932308 AGTTTCACTCTTGTTCCCCAGGCTGGAGTACAATGGCACCATCTCAGCTCGCCGCAACCTCCACC AGTTTCACTCTTGTTCCCCAGGCTGGAGTACAGTGGCACCATCTCAGCTCGCCGCAACCTCCACC T C AC093827.4,AC093827.5 Ensembl:ENSG00000284968,Ensembl:ENSG00000285458 lincRNA,Protein coding exon,5'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1327962341 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_580926,Human_Splice_Rec_580927,Human_Splice_Rec_580946,Human_Splice_Rec_580947,Human_Splice_Rec_580952,Human_Splice_Rec_580953 RMVar_hsa_circ_357887 17999 RMVar_ID_17999 Human_SNP_ID_192874504 A-to-I Human chr4 + 86938351 86938351 86938351 GTGCTCCTGTAATTACGCTTCCTCGGGAGGCTAAGGCAGGAAAGTCGCTTGAACCCAGGAGGCGG GTGCTCCTGTAATTACGCTTCCTCGGGAGGCTGAGGCAGGAAAGTCGCTTGAACCCAGGAGGCGG A G AFF1 Ensembl:ENSG00000172493 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1032403384 Functional Loss SNV dbSNP153 33..33 33 - - - 18000 RMVar_ID_18000 Human_SNP_ID_192875153 A-to-I Human chr4 + 86940967 86940967 86940967 AAAATTAGCCGGGTATTGTGTTGGACACCTGTAATCCCAGCTACTTGGGAGGCTGAGGGAGGAGA AAAATTAGCCGGGTATTGTGTTGGACACCTGTGATCCCAGCTACTTGGGAGGCTGAGGGAGGAGA A G AFF1 Ensembl:ENSG00000172493 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1015450535 Functional Loss SNV dbSNP153 33..33 33 - - - 18001 RMVar_ID_18001 Human_SNP_ID_192879965 A-to-I Human chr4 + 86958197 86958197 86958197 CTCACTGCAACTTCCACCTCTCAGGTTCAAGCAATTCTTCTGCCTCAGCCTCCCGAGTAGCTGAG CTCACTGCAACTTCCACCTCTCAGGTTCAAGCGATTCTTCTGCCTCAGCCTCCCGAGTAGCTGAG A G AFF1 Ensembl:ENSG00000172493 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs13109812 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_355934,RMVar_hsa_circ_365059,RMVar_hsa_circ_227318,RMVar_hsa_circ_311450 18002 RMVar_ID_18002 Human_SNP_ID_192880008 A-to-I Human chr4 + 86958351 86958351 86958351 GACCTCAAGTGATCTGCCCAACTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGTCACCGTG GACCTCAAGTGATCTGCCCAACTCAGCCTCCCGAAGTGCTGGGATTACAGGCGTGAGTCACCGTG A G AFF1 Ensembl:ENSG00000172493 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1402929909 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_355934,RMVar_hsa_circ_365059,RMVar_hsa_circ_227318,RMVar_hsa_circ_311450 18003 RMVar_ID_18003 Human_SNP_ID_192881486 A-to-I Human chr4 + 86964032 86964032 86964032 TAGACCTGGGATCTCACCATGTTGCCCAAGCTAGTTCTGAACTCCTGGCCTCAAGCAGTCCTCCT TAGACCTGGGATCTCACCATGTTGCCCAAGCTGGTTCTGAACTCCTGGCCTCAAGCAGTCCTCCT A G AFF1 Ensembl:ENSG00000172493 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs534059017 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_355934,RMVar_hsa_circ_365059,RMVar_hsa_circ_227318,RMVar_hsa_circ_311450 18004 RMVar_ID_18004 Human_SNP_ID_192883507 A-to-I Human chr4 + 86971879 86971879 86971879 TGAAGGGGCGCTGGGTAGGTTGGCTTATGCCTATTATCCCAGCACTTGGGGAGGCTAAGACTGGA TGAAGGGGCGCTGGGTAGGTTGGCTTATGCCTGTTATCCCAGCACTTGGGGAGGCTAAGACTGGA A G AFF1 Ensembl:ENSG00000172493 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs867504390 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_355934,RMVar_hsa_circ_365059,RMVar_hsa_circ_227318,RMVar_hsa_circ_311450 18005 RMVar_ID_18005 Human_SNP_ID_192883544 A-to-I Human chr4 + 86972001 86972001 86972001 TCTACAAAAACTTCAAAAGATTAGTCGGGAATAGTGGCACATGCCTGTAGACTCAGCTACATGGG TCTACAAAAACTTCAAAAGATTAGTCGGGAATCGTGGCACATGCCTGTAGACTCAGCTACATGGG A C AFF1 Ensembl:ENSG00000172493 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1373376722 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_355934,RMVar_hsa_circ_365059,RMVar_hsa_circ_227318,RMVar_hsa_circ_311450 18006 RMVar_ID_18006 Human_SNP_ID_192883552 A-to-I Human chr4 + 86972027 86972027 86972027 GGGAATAGTGGCACATGCCTGTAGACTCAGCTACATGGGAGGTTGAAGTGGGAGAATCACTTGAG GGGAATAGTGGCACATGCCTGTAGACTCAGCTGCATGGGAGGTTGAAGTGGGAGAATCACTTGAG A G AFF1 Ensembl:ENSG00000172493 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs747702086 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_355934,RMVar_hsa_circ_365059,RMVar_hsa_circ_227318,RMVar_hsa_circ_311450 18007 RMVar_ID_18007 Human_SNP_ID_192884123 A-to-I Human chr4 + 86974273 86974273 86974273 AGCTTCAAGTGATTCTCCTGCCTCAGCCTCCCAAGTGGCTGGAGTTACAGGCACATGCCACCACG AGCTTCAAGTGATTCTCCTGCCTCAGCCTCCCTAGTGGCTGGAGTTACAGGCACATGCCACCACG A T AFF1 Ensembl:ENSG00000172493 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232477135 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_355934,RMVar_hsa_circ_365059,RMVar_hsa_circ_227318,RMVar_hsa_circ_311450 18008 RMVar_ID_18008 Human_SNP_ID_192885393 A-to-I Human chr4 + 86979360 86979360 86979360 ACCTCAGGTGATCCTCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGGATGAGCCACTGCCC ACCTCAGGTGATCCTCCCGCCTCGGCCTCCCAGAGTGCTGGGATTACAGGGATGAGCCACTGCCC A G AFF1 Ensembl:ENSG00000172493 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991135957 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_355934,RMVar_hsa_circ_365059,RMVar_hsa_circ_227318,RMVar_hsa_circ_311450 18009 RMVar_ID_18009 Human_SNP_ID_192886944 A-to-I Human chr4 + 86984391 86984391 86984391 GCTCTGTTGCCCAGGCTGAGGTGCAGTGGTGCAATCTCAGCTCACGCAACTTCTGTCTCCTGGAT GCTCTGTTGCCCAGGCTGAGGTGCAGTGGTGCTATCTCAGCTCACGCAACTTCTGTCTCCTGGAT A T AFF1 Ensembl:ENSG00000172493 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1304801034 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_355934,RMVar_hsa_circ_365059,RMVar_hsa_circ_227318,RMVar_hsa_circ_311450 18010 RMVar_ID_18010 Human_SNP_ID_192886988 A-to-I Human chr4 + 86984513 86984512 86984513 GCAGCTAATTTCTTTTGTGTTTTAGTAGAGACAGGGTTTCACCGTGTTGCCCAGGCTAGTCTCGA GCAGCTAATTTCTTTTGTGTTTTAGTAGAGAC_GGGTTTCACCGTGTTGCCCAGGCTAGTCTCGA CA C AFF1 Ensembl:ENSG00000172493 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223751694 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_355934,RMVar_hsa_circ_365059,RMVar_hsa_circ_227318,RMVar_hsa_circ_311450 18011 RMVar_ID_18011 Human_SNP_ID_192886989 A-to-I Human chr4 + 86984513 86984512 86984514 GCAGCTAATTTCTTTTGTGTTTTAGTAGAGACAGGGTTTCACCGTGTTGCCCAGGCTAGTCTCGA GCAGCTAATTTCTTTTGTGTTTTAGTAGAGAC__GGTTTCACCGTGTTGCCCAGGCTAGTCTCGA CAG C AFF1 Ensembl:ENSG00000172493 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1250715123 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_355934,RMVar_hsa_circ_365059,RMVar_hsa_circ_227318,RMVar_hsa_circ_311450 18012 RMVar_ID_18012 Human_SNP_ID_192887877 A-to-I Human chr4 + 86987045 86987045 86987045 ATATTATTTTTTGTAGAGATGGGGGTCTTGCTATGTTGCCCAGGCTGGTCTCAAACTGCTGGCAT ATATTATTTTTTGTAGAGATGGGGGTCTTGCTCTGTTGCCCAGGCTGGTCTCAAACTGCTGGCAT A C AFF1 Ensembl:ENSG00000172493 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs905279065 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_355934,RMVar_hsa_circ_365059,RMVar_hsa_circ_227318,RMVar_hsa_circ_311450 18013 RMVar_ID_18013 Human_SNP_ID_192887878 A-to-I Human chr4 + 86987045 86987045 86987045 ATATTATTTTTTGTAGAGATGGGGGTCTTGCTATGTTGCCCAGGCTGGTCTCAAACTGCTGGCAT ATATTATTTTTTGTAGAGATGGGGGTCTTGCTGTGTTGCCCAGGCTGGTCTCAAACTGCTGGCAT A G AFF1 Ensembl:ENSG00000172493 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs905279065 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_355934,RMVar_hsa_circ_365059,RMVar_hsa_circ_227318,RMVar_hsa_circ_311450 18014 RMVar_ID_18014 Human_SNP_ID_192887879 A-to-I Human chr4 + 86987045 86987045 86987045 ATATTATTTTTTGTAGAGATGGGGGTCTTGCTATGTTGCCCAGGCTGGTCTCAAACTGCTGGCAT ATATTATTTTTTGTAGAGATGGGGGTCTTGCTTTGTTGCCCAGGCTGGTCTCAAACTGCTGGCAT A T AFF1 Ensembl:ENSG00000172493 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs905279065 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_355934,RMVar_hsa_circ_365059,RMVar_hsa_circ_227318,RMVar_hsa_circ_311450 18015 RMVar_ID_18015 Human_SNP_ID_192889664 A-to-I Human chr4 + 86993865 86993865 86993865 GTGTGCCTGTAATTCCAGCTACTCGGGAGGCTAAGGCAGGAGAATCATGTGAACCCAGGAGGTGG GTGTGCCTGTAATTCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCATGTGAACCCAGGAGGTGG A G AFF1 Ensembl:ENSG00000172493 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs951645819 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2862595 RMVar_hsa_circ_355934,RMVar_hsa_circ_365059,RMVar_hsa_circ_227318,RMVar_hsa_circ_311450 18016 RMVar_ID_18016 Human_SNP_ID_192890912 A-to-I Human chr4 + 86997186 86997186 86997186 CGCCCGCCTTGGCCCCCCAAAGTGCTGGGATTACAGGCATGAGCCACCACGCTTGGCCTGAACTG CGCCCGCCTTGGCCCCCCAAAGTGCTGGGATTGCAGGCATGAGCCACCACGCTTGGCCTGAACTG A G AFF1 Ensembl:ENSG00000172493 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1318025467 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23191307 RMVar_hsa_circ_355934,RMVar_hsa_circ_365059,RMVar_hsa_circ_227318,RMVar_hsa_circ_311450 18017 RMVar_ID_18017 Human_SNP_ID_192890914 A-to-I Human chr4 + 86997192 86997192 86997192 CCTTGGCCCCCCAAAGTGCTGGGATTACAGGCATGAGCCACCACGCTTGGCCTGAACTGGTGGCT CCTTGGCCCCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCACGCTTGGCCTGAACTGGTGGCT A G AFF1 Ensembl:ENSG00000172493 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs910116985 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_355934,RMVar_hsa_circ_365059,RMVar_hsa_circ_227318,RMVar_hsa_circ_311450 18018 RMVar_ID_18018 Human_SNP_ID_192890915 A-to-I Human chr4 + 86997192 86997192 86997192 CCTTGGCCCCCCAAAGTGCTGGGATTACAGGCATGAGCCACCACGCTTGGCCTGAACTGGTGGCT CCTTGGCCCCCCAAAGTGCTGGGATTACAGGCTTGAGCCACCACGCTTGGCCTGAACTGGTGGCT A T AFF1 Ensembl:ENSG00000172493 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs910116985 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_355934,RMVar_hsa_circ_365059,RMVar_hsa_circ_227318,RMVar_hsa_circ_311450 18019 RMVar_ID_18019 Human_SNP_ID_192890984 A-to-I Human chr4 + 86997491 86997491 86997491 AATATTTAAAAATGCATACTTGGGCTGGGCGCAGTGGCTCATGCCTGTAATCCCAGCACTTTGGG AATATTTAAAAATGCATACTTGGGCTGGGCGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGG A G AFF1 Ensembl:ENSG00000172493 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs779494916 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_355934,RMVar_hsa_circ_365059,RMVar_hsa_circ_227318,RMVar_hsa_circ_311450 18020 RMVar_ID_18020 Human_SNP_ID_192891014 A-to-I Human chr4 + 86997590 86997590 86997590 CGAGACCATCCTGGCCAACACGGTGAAACCCCATCTCTACTAAAAATACAAAAAATTAGCCGAGT CGAGACCATCCTGGCCAACACGGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTAGCCGAGT A G AFF1 Ensembl:ENSG00000172493 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs986924385 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_355934,RMVar_hsa_circ_365059,RMVar_hsa_circ_227318,RMVar_hsa_circ_311450 18021 RMVar_ID_18021 Human_SNP_ID_192898595 A-to-I Human chr4 + 87023072 87023072 87023072 CTACAGGCAGGCACACACCACCATGCCCAGCTAATTTTTAATTTTTTTTTGTAGAGATGGGGTCT CTACAGGCAGGCACACACCACCATGCCCAGCTGATTTTTAATTTTTTTTTGTAGAGATGGGGTCT A G AFF1 Ensembl:ENSG00000172493 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334424938 Functional Loss SNV dbSNP153 33..33 33 - - - 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_227320,RMVar_hsa_circ_115837,RMVar_hsa_circ_227321,RMVar_hsa_circ_227319 18022 RMVar_ID_18022 Human_SNP_ID_192903298 A-to-I Human chr4 + 87041051 87041051 87041051 GTGTGCGCCACCACGCCCAGCTAATATTTTGTATTTTTAGTAGCCACAGGGTTTCACCACGTTGG GTGTGCGCCACCACGCCCAGCTAATATTTTGTGTTTTTAGTAGCCACAGGGTTTCACCACGTTGG A G AFF1 Ensembl:ENSG00000172493 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1480250705 Functional Loss SNV dbSNP153 33..33 33 - - - 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_227320,RMVar_hsa_circ_115837,RMVar_hsa_circ_227321,RMVar_hsa_circ_227319 18023 RMVar_ID_18023 Human_SNP_ID_192919792 A-to-I Human chr4 + 87101312 87101312 87101312 TGAAAATGCCAGGATTCTACGGCCAGGCTCACACCTGTAATCCCAACACTTTGGGAGGCTGAAAT TGAAAATGCCAGGATTCTACGGCCAGGCTCACGCCTGTAATCCCAACACTTTGGGAGGCTGAAAT A G AFF1 Ensembl:ENSG00000172493 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1377579442 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 18024 RMVar_ID_18024 Human_SNP_ID_192928705 A-to-I Human chr4 + 87134101 87134101 87134101 GCTGTGATATATCCAGGGTATCCACAGTGTCTAAAAGAATGCATGGTACAGAGCAGGTGCTCAGT GCTGTGATATATCCAGGGTATCCACAGTGTCTGAAAGAATGCATGGTACAGAGCAGGTGCTCAGT A G AFF1 Ensembl:ENSG00000172493 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1441393564 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15220038 RMVar_hsa_circ_227330,RMVar_hsa_circ_109186 18025 RMVar_ID_18025 Human_SNP_ID_192930987 A-to-I Human chr4 + 87142740 87142740 87142740 CTCCCACCTCCACCTCCTGAGTAGTGGGGACTACAGGCACATGCCATCACGCCCAGCTAATTTTT CTCCCACCTCCACCTCCTGAGTAGTGGGGACTGCAGGCACATGCCATCACGCCCAGCTAATTTTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1380136230 Functional Loss SNV dbSNP153 33..33 33 - - - 18026 RMVar_ID_18026 Human_SNP_ID_192932306 A-to-I Human chr4 + 87147539 87147539 87147539 CCAAAATCCAAGGATGCTGAAGTCCCTGATATAAAATGGTGAAGTATTTTCATATAATCTACACA CCAAAATCCAAGGATGCTGAAGTCCCTGATATGAAATGGTGAAGTATTTTCATATAATCTACACA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1560679777 Functional Loss SNV dbSNP153 33..33 33 - - - 18027 RMVar_ID_18027 Human_SNP_ID_192943014 A-to-I Human chr4 - 87191412 87191412 87191412 TGTCACCCAGGCTGGAGTACAGTGATGCAGTCATGGGTCATGGCAACCTCCACCTCCTGGACCCA TGTCACCCAGGCTGGAGTACAGTGATGCAGTCTTGGGTCATGGCAACCTCCACCTCCTGGACCCA T A KLHL8 Ensembl:ENSG00000145332 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs534094706 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_227334,RMVar_hsa_circ_227335,RMVar_hsa_circ_227340,RMVar_hsa_circ_287916,RMVar_hsa_circ_227339,RMVar_hsa_circ_227346,RMVar_hsa_circ_227342,RMVar_hsa_circ_70514,RMVar_hsa_circ_227341,RMVar_hsa_circ_96411,RMVar_hsa_circ_291461,RMVar_hsa_circ_227344,RMVar_hsa_circ_227345,RMVar_hsa_circ_273704,RMVar_hsa_circ_75557 18028 RMVar_ID_18028 Human_SNP_ID_192943015 A-to-I Human chr4 - 87191412 87191412 87191412 TGTCACCCAGGCTGGAGTACAGTGATGCAGTCATGGGTCATGGCAACCTCCACCTCCTGGACCCA TGTCACCCAGGCTGGAGTACAGTGATGCAGTCGTGGGTCATGGCAACCTCCACCTCCTGGACCCA T C KLHL8 Ensembl:ENSG00000145332 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs534094706 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_227334,RMVar_hsa_circ_227335,RMVar_hsa_circ_227340,RMVar_hsa_circ_287916,RMVar_hsa_circ_227339,RMVar_hsa_circ_227346,RMVar_hsa_circ_227342,RMVar_hsa_circ_70514,RMVar_hsa_circ_227341,RMVar_hsa_circ_96411,RMVar_hsa_circ_291461,RMVar_hsa_circ_227344,RMVar_hsa_circ_227345,RMVar_hsa_circ_273704,RMVar_hsa_circ_75557 18029 RMVar_ID_18029 Human_SNP_ID_192943017 A-to-I Human chr4 - 87191416 87191416 87191416 GCTCTGTCACCCAGGCTGGAGTACAGTGATGCAGTCATGGGTCATGGCAACCTCCACCTCCTGGA GCTCTGTCACCCAGGCTGGAGTACAGTGATGCTGTCATGGGTCATGGCAACCTCCACCTCCTGGA T A KLHL8 Ensembl:ENSG00000145332 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1470838189 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_227334,RMVar_hsa_circ_227335,RMVar_hsa_circ_227340,RMVar_hsa_circ_287916,RMVar_hsa_circ_227339,RMVar_hsa_circ_227346,RMVar_hsa_circ_227342,RMVar_hsa_circ_70514,RMVar_hsa_circ_227341,RMVar_hsa_circ_96411,RMVar_hsa_circ_291461,RMVar_hsa_circ_227344,RMVar_hsa_circ_227345,RMVar_hsa_circ_273704,RMVar_hsa_circ_75557 18030 RMVar_ID_18030 Human_SNP_ID_192943263 A-to-I Human chr4 - 87192523 87192523 87192523 TGCTGGGATATAAGCCTGCGTAGCCTATTACCATACTGAAAACTGTATGCAGTTGTAACACAATG TGCTGGGATATAAGCCTGCGTAGCCTATTACCGTACTGAAAACTGTATGCAGTTGTAACACAATG T C KLHL8 Ensembl:ENSG00000145332 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs539289073 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_227334,RMVar_hsa_circ_227335,RMVar_hsa_circ_227340,RMVar_hsa_circ_287916,RMVar_hsa_circ_227339,RMVar_hsa_circ_227346,RMVar_hsa_circ_227342,RMVar_hsa_circ_70514,RMVar_hsa_circ_227341,RMVar_hsa_circ_96411,RMVar_hsa_circ_291461,RMVar_hsa_circ_227344,RMVar_hsa_circ_227345,RMVar_hsa_circ_273704,RMVar_hsa_circ_75557 18031 RMVar_ID_18031 Human_SNP_ID_193000619 A-to-I Human chr4 + 87426774 87426774 87426774 AAAGGATAATATGGCCTGGTGTGGAGGCTCACACCTGTAATCTCAGCACTTTGGAAGTCCGAGGC AAAGGATAATATGGCCTGGTGTGGAGGCTCACGCCTGTAATCTCAGCACTTTGGAAGTCCGAGGC A G NUDT9 Ensembl:ENSG00000170502 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355781252 Functional Loss SNV dbSNP153 33..33 33 - - - 18032 RMVar_ID_18032 Human_SNP_ID_193003063 A-to-I Human chr4 + 87437113 87437113 87437113 TATACCAAAAATATAAAAAATTAGCTGGGTATAGTGGCATGTTCCTGTAGTCCCAGCTACTCAGC TATACCAAAAATATAAAAAATTAGCTGGGTATGGTGGCATGTTCCTGTAGTCCCAGCTACTCAGC A G NUDT9 Ensembl:ENSG00000170502 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs954517720 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_329757,RMVar_hsa_circ_331803,RMVar_hsa_circ_328664 18033 RMVar_ID_18033 Human_SNP_ID_193004105 A-to-I Human chr4 + 87440725 87440725 87440725 AAAATTAGCTGGGCGTGGTGGTGCATGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA AAAATTAGCTGGGCGTGGTGGTGCATGCCTGTCATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA A C NUDT9 Ensembl:ENSG00000170502 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs891734437 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_227356,RMVar_hsa_circ_331803,RMVar_hsa_circ_328664,RMVar_hsa_circ_302112 18034 RMVar_ID_18034 Human_SNP_ID_193004106 A-to-I Human chr4 + 87440725 87440725 87440725 AAAATTAGCTGGGCGTGGTGGTGCATGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA AAAATTAGCTGGGCGTGGTGGTGCATGCCTGTGATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA A G NUDT9 Ensembl:ENSG00000170502 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs891734437 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_227356,RMVar_hsa_circ_331803,RMVar_hsa_circ_328664,RMVar_hsa_circ_302112 18035 RMVar_ID_18035 Human_SNP_ID_193113169 A-to-I Human chr4 + 87892503 87892503 87892503 CTATCCCATCACCCTTTATTTGGAGAAGGAACAAGACAAGGAAATTAGTGATGATGAGGCAGAAG CTATCCCATCACCCTTTATTTGGAGAAGGAACGAGACAAGGAAATTAGTGATGATGAGGCAGAAG A G HSP90AB3P Ensembl:ENSG00000183199 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879027927 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3749892 18036 RMVar_ID_18036 Human_SNP_ID_193113377 A-to-I Human chr4 + 87892974 87892974 87892974 TGAGTTGATACCAGAGTATCTCAATTTTATCCATGGTGTGGTTGACTCTGAGGATCTGCCCCTGA TGAGTTGATACCAGAGTATCTCAATTTTATCCGTGGTGTGGTTGACTCTGAGGATCTGCCCCTGA A G HSP90AB3P Ensembl:ENSG00000183199 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs765948573 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1107083,Human_RBP_ID_8265953,Human_RBP_ID_9261661,Human_RBP_ID_17706440,Human_RBP_ID_18032672,Human_RBP_ID_18409615,Human_RBP_ID_18517861,Human_RBP_ID_21082880,Human_RBP_ID_22511101 18037 RMVar_ID_18037 Human_SNP_ID_193135421 A-to-I Human chr4 + 87982558 87982558 87982558 ACATGGAAAGCGAGGAGTTGAATGGTGCATACAAGGCCATCCCCGTTGCCCAGGACCTGAACGCG ACATGGAAAGCGAGGAGTTGAATGGTGCATACGAGGCCATCCCCGTTGCCCAGGACCTGAACGCG A G SPP1 Ensembl:ENSG00000118785 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1222227364 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_786438,Human_RBP_ID_22458360,Human_RBP_ID_22770745 Human_Splice_Rec_581698,Human_Splice_Rec_581708,Human_Splice_Rec_581744,Human_Splice_Rec_581754,Human_Splice_Rec_581766,Human_Splice_Rec_581780 18038 RMVar_ID_18038 Human_SNP_ID_193144369 A-to-I Human chr4 + 88020783 88020783 88020783 ACAATCATAGCTCACTGCAGCCTCGAGCTCCTAGGCTTCAGTGATCCTCCCACCTCAGTCACCCA ACAATCATAGCTCACTGCAGCCTCGAGCTCCTGGGCTTCAGTGATCCTCCCACCTCAGTCACCCA A G PKD2 Ensembl:ENSG00000118762 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1255163831 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_555,RMVar_hsa_circ_227363,RMVar_hsa_circ_88796,RMVar_hsa_circ_101960,RMVar_hsa_circ_227364,RMVar_hsa_circ_286873,RMVar_hsa_circ_333624,RMVar_hsa_circ_377489,RMVar_hsa_circ_344316,RMVar_hsa_circ_303872,RMVar_hsa_circ_13605,RMVar_hsa_circ_281350,RMVar_hsa_circ_6172,RMVar_hsa_circ_227366,RMVar_hsa_circ_227368,RMVar_hsa_circ_227369,RMVar_hsa_circ_227367 18039 RMVar_ID_18039 Human_SNP_ID_193161120 A-to-I Human chr4 - 88089588 88089588 88089588 TACTTTATAAGAAAATAAACCACACTTTAAAAAAGTTCCTTAATTTTAAAATGGTTAAGATGGTA TACTTTATAAGAAAATAAACCACACTTTAAAATAGTTCCTTAATTTTAAAATGGTTAAGATGGTA T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1200671628 Functional Loss SNV dbSNP153 33..33 33 - - - 18040 RMVar_ID_18040 Human_SNP_ID_193161125 A-to-I Human chr4 - 88089614 88089614 88089614 GGTATGTATATCCTTAAGTAAATTTCTACTTTATAAGAAAATAAACCACACTTTAAAAAAGTTCC GGTATGTATATCCTTAAGTAAATTTCTACTTTGTAAGAAAATAAACCACACTTTAAAAAAGTTCC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs190284181 Functional Loss SNV dbSNP153 33..33 33 - - - 18041 RMVar_ID_18041 Human_SNP_ID_193161126 A-to-I Human chr4 - 88089614 88089614 88089614 GGTATGTATATCCTTAAGTAAATTTCTACTTTATAAGAAAATAAACCACACTTTAAAAAAGTTCC GGTATGTATATCCTTAAGTAAATTTCTACTTTCTAAGAAAATAAACCACACTTTAAAAAAGTTCC T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs190284181 Functional Loss SNV dbSNP153 33..33 33 - - - 18042 RMVar_ID_18042 Human_SNP_ID_193161129 A-to-I Human chr4 - 88089619 88089619 88089619 ATATGGGTATGTATATCCTTAAGTAAATTTCTACTTTATAAGAAAATAAACCACACTTTAAAAAA ATATGGGTATGTATATCCTTAAGTAAATTTCTGCTTTATAAGAAAATAAACCACACTTTAAAAAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs949003626 Functional Loss SNV dbSNP153 33..33 33 - - - 18043 RMVar_ID_18043 Human_SNP_ID_193167402 A-to-I Human chr4 - 88115944 88115944 88115944 GTGGTTTGCTGGTCTCGGCCTCCCGAAGTGCTAGTATTACAGATGTGAGCCATTGCACCCAGCGC GTGGTTTGCTGGTCTCGGCCTCCCGAAGTGCTGGTATTACAGATGTGAGCCATTGCACCCAGCGC T C ABCG2 Ensembl:ENSG00000118777 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1406485865 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35418,RMVar_hsa_circ_227403,RMVar_hsa_circ_102335,RMVar_hsa_circ_350172,RMVar_hsa_circ_352746,RMVar_hsa_circ_30889,RMVar_hsa_circ_364801,RMVar_hsa_circ_366162,RMVar_hsa_circ_67959,RMVar_hsa_circ_51780 18044 RMVar_ID_18044 Human_SNP_ID_193175337 A-to-I Human chr4 - 88149751 88149751 88149751 TGCCTCCCAGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCCGAGTGGCTGGGGTTACAGGCATGCG TGCCTCCCAGGTTCAAGCAGTTCTCCTGCCTCCGCCTCCCGAGTGGCTGGGGTTACAGGCATGCG T G ABCG2 Ensembl:ENSG00000118777 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1299865575 Functional Loss SNV dbSNP153 33..33 33 - - - 18045 RMVar_ID_18045 Human_SNP_ID_193201455 A-to-I Human chr4 - 88258443 88258443 88258443 TTGTATTTTTAGTAGAGACAGGGTTTCACCATATTGGCCAGGATGGTCTCGATCTCTTGACCTCG TTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGATGGTCTCGATCTCTTGACCTCG T C PPM1K Ensembl:ENSG00000163644 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1048042101 Functional Loss SNV dbSNP153 33..33 33 - - - 18046 RMVar_ID_18046 Human_SNP_ID_193201559 A-to-I Human chr4 - 88258840 88258840 88258840 CCTCAAGTGATCCACCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCACC CCTCAAGTGATCCACCCACCTCGGCCTCCCAAGGTGCTGGGATTACAGGCATGAGCCACCGCACC T C PPM1K Ensembl:ENSG00000163644 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1303233689 Functional Loss SNV dbSNP153 33..33 33 - - - 18047 RMVar_ID_18047 Human_SNP_ID_193201677 A-to-I Human chr4 - 88259230 88259230 88259230 ATGGAGTCTCACTCTGTCACACAGGCTGGAGTACAGTGGTGCGGTCTCGGCTCCCTGCAACCTCT ATGGAGTCTCACTCTGTCACACAGGCTGGAGTGCAGTGGTGCGGTCTCGGCTCCCTGCAACCTCT T C PPM1K Ensembl:ENSG00000163644 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1372981839 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7337375 18048 RMVar_ID_18048 Human_SNP_ID_193201910 A-to-I Human chr4 - 88260190 88260190 88260190 AAAATTAGCCAGGCGTGGTGGTGGGTGCCTGTAATCCCAGCTACTGGGGAGGCTGAGGAAGGAGA AAAATTAGCCAGGCGTGGTGGTGGGTGCCTGTTATCCCAGCTACTGGGGAGGCTGAGGAAGGAGA T A PPM1K Ensembl:ENSG00000163644 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1047759434 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25826246 18049 RMVar_ID_18049 Human_SNP_ID_193201923 A-to-I Human chr4 - 88260227 88260227 88260227 CCAACATGGTGAAACCTCATCTTGACCAAAAAATGCAAAAATTAGCCAGGCGTGGTGGTGGGTGC CCAACATGGTGAAACCTCATCTTGACCAAAAAGTGCAAAAATTAGCCAGGCGTGGTGGTGGGTGC T C PPM1K Ensembl:ENSG00000163644 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1276211909 Functional Loss SNV dbSNP153 33..33 33 - - - 18050 RMVar_ID_18050 Human_SNP_ID_193202250 A-to-I Human chr4 - 88261759 88261759 88261759 CCAGGAGATGGGGGTTGCAGTGAGCTGAGATCATGCCATTGCACTCCAGCCTGGGCAGCAAGAGC CCAGGAGATGGGGGTTGCAGTGAGCTGAGATCTTGCCATTGCACTCCAGCCTGGGCAGCAAGAGC T A PPM1K Ensembl:ENSG00000163644 Protein coding 3'UTR GSE38233;GSE107867 cultured B-cells;ASD brains,temporal_cortex - 24183664,30559470 RNA-Seq:(High) rs1201266573 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10158994,Human_RBP_ID_25836279 RMVar_hsa_circ_78079,RMVar_hsa_circ_227406 18051 RMVar_ID_18051 Human_SNP_ID_193236181 A-to-I Human chr4 + 88399656 88399656 88399656 AGCTGGGAGTGGTGGTACGAGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATTGTT AGCTGGGAGTGGTGGTACGAGCCTGTAATCCCCGCTACTTGGGAGGCTGAGGCAGGAGAATTGTT A C HERC6 Ensembl:ENSG00000138642 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1455247151 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117912,RMVar_hsa_circ_352159,RMVar_hsa_circ_356772,RMVar_hsa_circ_46835,RMVar_hsa_circ_227411 18052 RMVar_ID_18052 Human_SNP_ID_193248485 A-to-I Human chr4 - 88456737 88456737 88456737 GCCGCGGCCGGGCGCGGTGATTCACGCCTGTAATCCCAGCACTTTGGGGGGCCGAGGCGGGCGGA GCCGCGGCCGGGCGCGGTGATTCACGCCTGTAGTCCCAGCACTTTGGGGGGCCGAGGCGGGCGGA T C lnc-PYURF-3,lnc-PYURF-3:2,lnc-PYURF-3:3,lnc-PYURF-3:4,lnc-PYURF-3:5 RNACentral:URS0000D5AE77,RNACentral:URS0000D59BB2,RNACentral:URS0000D5747F,RNACentral:URS0000D59EB6,RNACentral:URS0000D5BE07 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,exon,exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs895668223 Functional Loss SNV dbSNP153 33..33 33 - - - 18053 RMVar_ID_18053 Human_SNP_ID_193260153 A-to-I Human chr4 + 88503886 88503886 88503886 CAGGAGTTTGAGAGCAGCCTGGCCAACATGGTAAAACCCCATCTCTACTAAAAATACAAAAAAAT CAGGAGTTTGAGAGCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAAAAT A G HERC5 Ensembl:ENSG00000138646 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1560616909 Functional Loss SNV dbSNP153 33..33 33 - - - 18054 RMVar_ID_18054 Human_SNP_ID_193282908 A-to-I Human chr4 + 88602514 88602514 88602514 TGCTTGTTTGTTTTTAAGATGGGTCTCGCTCTATTACCCAGGCTGGAGTGCAGCAGTGCGATCAC TGCTTGTTTGTTTTTAAGATGGGTCTCGCTCTGTTACCCAGGCTGGAGTGCAGCAGTGCGATCAC A G AC098582.1,HERC3 Ensembl:ENSG00000287542,Ensembl:ENSG00000138641 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs902027211 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13437,RMVar_hsa_circ_120721,RMVar_hsa_circ_33005,RMVar_hsa_circ_227425 18055 RMVar_ID_18055 Human_SNP_ID_193302772 A-to-I Human chr4 + 88689398 88689398 88689398 AATTAGCCAGGTGTGTGGCAGTGCACATCTGTAGTTCCAGCTACTCAGGAGGCTAAGGTGGGAGG AATTAGCCAGGTGTGTGGCAGTGCACATCTGTGGTTCCAGCTACTCAGGAGGCTAAGGTGGGAGG A G AC098582.1,HERC3 Ensembl:ENSG00000287542,Ensembl:ENSG00000138641 Protein coding,Protein coding intron,intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1404674178 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13437,RMVar_hsa_circ_322675,RMVar_hsa_circ_11053,RMVar_hsa_circ_6334,RMVar_hsa_circ_323906,RMVar_hsa_circ_227441 18056 RMVar_ID_18056 Human_SNP_ID_193302777 A-to-I Human chr4 + 88689412 88689412 88689412 GTGGCAGTGCACATCTGTAGTTCCAGCTACTCAGGAGGCTAAGGTGGGAGGATCACTTGAGCTTG GTGGCAGTGCACATCTGTAGTTCCAGCTACTCGGGAGGCTAAGGTGGGAGGATCACTTGAGCTTG A G AC098582.1,HERC3 Ensembl:ENSG00000287542,Ensembl:ENSG00000138641 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1376669034 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13437,RMVar_hsa_circ_322675,RMVar_hsa_circ_11053,RMVar_hsa_circ_6334,RMVar_hsa_circ_323906,RMVar_hsa_circ_227441 18057 RMVar_ID_18057 Human_SNP_ID_193331148 A-to-I Human chr4 - 88814907 88814907 88814907 CCAGGAGTTTGAGGCTGCAGTGAGGTATGATCATGCCACTGTACTCCAGCCTAGATGACAGATTA CCAGGAGTTTGAGGCTGCAGTGAGGTATGATCGTGCCACTGTACTCCAGCCTAGATGACAGATTA T C FAM13A Ensembl:ENSG00000138640 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1343971977 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10159154 RMVar_hsa_circ_5962,RMVar_hsa_circ_227448,RMVar_hsa_circ_79437,RMVar_hsa_circ_72066,RMVar_hsa_circ_82599,RMVar_hsa_circ_227455,RMVar_hsa_circ_43246 18058 RMVar_ID_18058 Human_SNP_ID_193348755 A-to-I Human chr4 - 88888812 88888812 88888812 CCTGCCTCAGCCTCCTGAGTAGCTGGGACTGCAGGTACCCGCCAACACACCCGGCTAATTTTTTT CCTGCCTCAGCCTCCTGAGTAGCTGGGACTGCGGGTACCCGCCAACACACCCGGCTAATTTTTTT T C FAM13A Ensembl:ENSG00000138640 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909210210 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5962,RMVar_hsa_circ_227448,RMVar_hsa_circ_79437,RMVar_hsa_circ_72066,RMVar_hsa_circ_82599,RMVar_hsa_circ_227455,RMVar_hsa_circ_41900,RMVar_hsa_circ_353550,RMVar_hsa_circ_15983 18059 RMVar_ID_18059 Human_SNP_ID_193371916 A-to-I Human chr4 - 88984746 88984746 88984746 GACTAATATAAAATAAATATTCAAAGAAAAATAAAACCTGAGGACCTAATAGGAAAATGGCAAAA GACTAATATAAAATAAATATTCAAAGAAAAATGAAACCTGAGGACCTAATAGGAAAATGGCAAAA T C FAM13A Ensembl:ENSG00000138640 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1323140715 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5962,RMVar_hsa_circ_72066,RMVar_hsa_circ_82599,RMVar_hsa_circ_227455,RMVar_hsa_circ_41900,RMVar_hsa_circ_353550,RMVar_hsa_circ_227462,RMVar_hsa_circ_227460,RMVar_hsa_circ_300827,RMVar_hsa_circ_360907,RMVar_hsa_circ_337268,RMVar_hsa_circ_338413,RMVar_hsa_circ_99442,RMVar_hsa_circ_227464,RMVar_hsa_circ_227461 18060 RMVar_ID_18060 Human_SNP_ID_193371919 A-to-I Human chr4 - 88984755 88984755 88984755 GCAAAAAGAGACTAATATAAAATAAATATTCAAAGAAAAATAAAACCTGAGGACCTAATAGGAAA GCAAAAAGAGACTAATATAAAATAAATATTCACAGAAAAATAAAACCTGAGGACCTAATAGGAAA T G FAM13A Ensembl:ENSG00000138640 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs913755002 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18031342,Human_RBP_ID_27731017 RMVar_hsa_circ_5962,RMVar_hsa_circ_72066,RMVar_hsa_circ_82599,RMVar_hsa_circ_227455,RMVar_hsa_circ_41900,RMVar_hsa_circ_353550,RMVar_hsa_circ_227462,RMVar_hsa_circ_227460,RMVar_hsa_circ_300827,RMVar_hsa_circ_360907,RMVar_hsa_circ_337268,RMVar_hsa_circ_338413,RMVar_hsa_circ_99442,RMVar_hsa_circ_227464,RMVar_hsa_circ_227461 18061 RMVar_ID_18061 Human_SNP_ID_193373166 A-to-I Human chr4 - 88989571 88989571 88989571 TTTTAAGACAGTCTCACTTTGTTACCCAGGCTAGAGTGCAGTGGTACAATCTCGGCTCACTGCAA TTTTAAGACAGTCTCACTTTGTTACCCAGGCTGGAGTGCAGTGGTACAATCTCGGCTCACTGCAA T C FAM13A Ensembl:ENSG00000138640 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs528444493 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2863832 RMVar_hsa_circ_5962,RMVar_hsa_circ_72066,RMVar_hsa_circ_82599,RMVar_hsa_circ_227455,RMVar_hsa_circ_41900,RMVar_hsa_circ_353550,RMVar_hsa_circ_227462,RMVar_hsa_circ_227460,RMVar_hsa_circ_300827,RMVar_hsa_circ_360907,RMVar_hsa_circ_337268,RMVar_hsa_circ_338413,RMVar_hsa_circ_99442,RMVar_hsa_circ_227464,RMVar_hsa_circ_227461 18062 RMVar_ID_18062 Human_SNP_ID_89278398 A-to-I Human chr2 + 120121028 120121028 120121028 AATCCCAGCCACTGGTGAGGATAAGGCAGGAGAATCGCCCAAACCCAGGAGGCAGAGGCCGCAGT AATCCCAGCCACTGGTGAGGATAAGGCAGGAGGATCGCCCAAACCCAGGAGGCAGAGGCCGCAGT A G EPB41L5 Ensembl:ENSG00000115109 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs911712461 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11061,RMVar_hsa_circ_17829,RMVar_hsa_circ_35568,RMVar_hsa_circ_42506,RMVar_hsa_circ_114724,RMVar_hsa_circ_108303,RMVar_hsa_circ_202909,RMVar_hsa_circ_202910,RMVar_hsa_circ_111445,RMVar_hsa_circ_102078,RMVar_hsa_circ_202914,RMVar_hsa_circ_202915,RMVar_hsa_circ_61694,RMVar_hsa_circ_202918,RMVar_hsa_circ_45337,RMVar_hsa_circ_12066,RMVar_hsa_circ_12505,RMVar_hsa_circ_317770,RMVar_hsa_circ_328614,RMVar_hsa_circ_34225,RMVar_hsa_circ_48959,RMVar_hsa_circ_26234,RMVar_hsa_circ_202927,RMVar_hsa_circ_202925,RMVar_hsa_circ_202926,RMVar_hsa_circ_40188,RMVar_hsa_circ_40417,RMVar_hsa_circ_109642,RMVar_hsa_circ_59707,RMVar_hsa_circ_202929,RMVar_hsa_circ_202928,RMVar_hsa_circ_202933 18063 RMVar_ID_18063 Human_SNP_ID_89587531 A-to-I Human chr2 - 121338612 121338612 121338612 AAAACTGCTGCCGCCGCGCCGAGGAGACTCGCATGCCGCCACCACCTCACTGGGAGGGCGCCGAG AAAACTGCTGCCGCCGCGCCGAGGAGACTCGCTTGCCGCCACCACCTCACTGGGAGGGCGCCGAG T A CLASP1 Ensembl:ENSG00000074054 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs796945071 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20436203,Human_RBP_ID_23821929 18064 RMVar_ID_18064 Human_SNP_ID_89587532 A-to-I Human chr2 - 121338612 121338612 121338612 AAAACTGCTGCCGCCGCGCCGAGGAGACTCGCATGCCGCCACCACCTCACTGGGAGGGCGCCGAG AAAACTGCTGCCGCCGCGCCGAGGAGACTCGCGTGCCGCCACCACCTCACTGGGAGGGCGCCGAG T C CLASP1 Ensembl:ENSG00000074054 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs796945071 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20436203,Human_RBP_ID_23821929 18065 RMVar_ID_18065 Human_SNP_ID_89588518 A-to-I Human chr2 - 121342413 121342413 121342413 TTTTCATTTGTCTCAAGATGTTTTCTAAGGCTAGGTGCGGTGGCTCACGCTAGTAATCCCAGCAC TTTTCATTTGTCTCAAGATGTTTTCTAAGGCTGGGTGCGGTGGCTCACGCTAGTAATCCCAGCAC T C CLASP1 Ensembl:ENSG00000074054 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1057083299 Functional Loss SNV dbSNP153 33..33 33 - - - 18066 RMVar_ID_18066 Human_SNP_ID_89588579 A-to-I Human chr2 - 121342706 121342706 121342706 CTTGAACTGGTTTCAAACGATTCTCCCACCTCAGCCTCCTACATTGCTGAGATTATAGGCGTGAC CTTGAACTGGTTTCAAACGATTCTCCCACCTCTGCCTCCTACATTGCTGAGATTATAGGCGTGAC T A CLASP1 Ensembl:ENSG00000074054 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1030266257 Functional Loss SNV dbSNP153 33..33 33 - - - 18067 RMVar_ID_18067 Human_SNP_ID_89588582 A-to-I Human chr2 - 121342722 121342722 121342722 ATGTTGCCAGTCTGGTCTTGAACTGGTTTCAAACGATTCTCCCACCTCAGCCTCCTACATTGCTG ATGTTGCCAGTCTGGTCTTGAACTGGTTTCAAGCGATTCTCCCACCTCAGCCTCCTACATTGCTG T C CLASP1 Ensembl:ENSG00000074054 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1403090569 Functional Loss SNV dbSNP153 33..33 33 - - - 18068 RMVar_ID_18068 Human_SNP_ID_89588596 A-to-I Human chr2 - 121342765 121342765 121342765 TCCCAGCTAATTTTTAAATTTTTTGTAGAGATAGGGTCTCGCTATGTTGCCAGTCTGGTCTTGAA TCCCAGCTAATTTTTAAATTTTTTGTAGAGATCGGGTCTCGCTATGTTGCCAGTCTGGTCTTGAA T G CLASP1 Ensembl:ENSG00000074054 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs978832206 Functional Loss SNV dbSNP153 33..33 33 - - - 18069 RMVar_ID_18069 Human_SNP_ID_89588852 A-to-I Human chr2 - 121343914 121343914 121343914 GGCGCCTGCCACCACGCCCAGCTAGTTTTTGTATTTTTAGTTGAGATGGGGTTTCACCATGTTGG GGCGCCTGCCACCACGCCCAGCTAGTTTTTGTGTTTTTAGTTGAGATGGGGTTTCACCATGTTGG T C CLASP1 Ensembl:ENSG00000074054 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs563536052 Functional Loss SNV dbSNP153 33..33 33 - - - 18070 RMVar_ID_18070 Human_SNP_ID_89594915 A-to-I Human chr2 - 121369140 121369140 121369140 ATAGCAGCATTATTCACAAGAGCCAAAAGGCAAAAGCAATCCAAGTGCCCATCAGCAGATGAACA ATAGCAGCATTATTCACAAGAGCCAAAAGGCAGAAGCAATCCAAGTGCCCATCAGCAGATGAACA T C CLASP1 Ensembl:ENSG00000074054 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs932710579 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3224,RMVar_hsa_circ_301920,RMVar_hsa_circ_121713,RMVar_hsa_circ_202962,RMVar_hsa_circ_335589,RMVar_hsa_circ_377955,RMVar_hsa_circ_305545,RMVar_hsa_circ_59229,RMVar_hsa_circ_40456,RMVar_hsa_circ_202965,RMVar_hsa_circ_7497,RMVar_hsa_circ_12677,RMVar_hsa_circ_5684,RMVar_hsa_circ_202966,RMVar_hsa_circ_202963,RMVar_hsa_circ_202964,RMVar_hsa_circ_43003,RMVar_hsa_circ_202968,RMVar_hsa_circ_113267 18071 RMVar_ID_18071 Human_SNP_ID_89603756 A-to-I Human chr2 - 121406728 121406728 121406728 AACATTAGCCGGATGTGGTGATATGCATCTGTAATCCCAGATACTTCGGAGGCTGAGGCAGGAGG AACATTAGCCGGATGTGGTGATATGCATCTGTGATCCCAGATACTTCGGAGGCTGAGGCAGGAGG T C CLASP1 Ensembl:ENSG00000074054 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1380728029 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569865 RMVar_hsa_circ_8,RMVar_hsa_circ_121713,RMVar_hsa_circ_202962,RMVar_hsa_circ_377955,RMVar_hsa_circ_305545,RMVar_hsa_circ_59229,RMVar_hsa_circ_7497,RMVar_hsa_circ_12677,RMVar_hsa_circ_202963,RMVar_hsa_circ_43003,RMVar_hsa_circ_2088,RMVar_hsa_circ_202968,RMVar_hsa_circ_113267,RMVar_hsa_circ_319935,RMVar_hsa_circ_332151,RMVar_hsa_circ_309232,RMVar_hsa_circ_35606,RMVar_hsa_circ_327706,RMVar_hsa_circ_6111,RMVar_hsa_circ_10357,RMVar_hsa_circ_202969,RMVar_hsa_circ_362716,RMVar_hsa_circ_330505,RMVar_hsa_circ_107706,RMVar_hsa_circ_116049,RMVar_hsa_circ_35773,RMVar_hsa_circ_84021,RMVar_hsa_circ_202971,RMVar_hsa_circ_202972,RMVar_hsa_circ_202973,RMVar_hsa_circ_336795,RMVar_hsa_circ_202975,RMVar_hsa_circ_340261,RMVar_hsa_circ_368071,RMVar_hsa_circ_274980,RMVar_hsa_circ_324156,RMVar_hsa_circ_63936,RMVar_hsa_circ_23997,RMVar_hsa_circ_41739,RMVar_hsa_circ_35866,RMVar_hsa_circ_202976,RMVar_hsa_circ_202977,RMVar_hsa_circ_202978,RMVar_hsa_circ_128046,RMVar_hsa_circ_202980,RMVar_hsa_circ_47852,RMVar_hsa_circ_335953,RMVar_hsa_circ_202979,RMVar_hsa_circ_362090,RMVar_hsa_circ_117254,RMVar_hsa_circ_202981,RMVar_hsa_circ_202982,RMVar_hsa_circ_95206,RMVar_hsa_circ_202983,RMVar_hsa_circ_115184,RMVar_hsa_circ_346673,RMVar_hsa_circ_349542,RMVar_hsa_circ_83520,RMVar_hsa_circ_202984,RMVar_hsa_circ_202985 18072 RMVar_ID_18072 Human_SNP_ID_89603762 A-to-I Human chr2 - 121406738 121406738 121406738 AAAAAGTTAAAACATTAGCCGGATGTGGTGATATGCATCTGTAATCCCAGATACTTCGGAGGCTG AAAAAGTTAAAACATTAGCCGGATGTGGTGATGTGCATCTGTAATCCCAGATACTTCGGAGGCTG T C CLASP1 Ensembl:ENSG00000074054 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs557307130 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569865 RMVar_hsa_circ_8,RMVar_hsa_circ_121713,RMVar_hsa_circ_202962,RMVar_hsa_circ_377955,RMVar_hsa_circ_305545,RMVar_hsa_circ_59229,RMVar_hsa_circ_7497,RMVar_hsa_circ_12677,RMVar_hsa_circ_202963,RMVar_hsa_circ_43003,RMVar_hsa_circ_2088,RMVar_hsa_circ_202968,RMVar_hsa_circ_113267,RMVar_hsa_circ_319935,RMVar_hsa_circ_332151,RMVar_hsa_circ_309232,RMVar_hsa_circ_35606,RMVar_hsa_circ_327706,RMVar_hsa_circ_6111,RMVar_hsa_circ_10357,RMVar_hsa_circ_202969,RMVar_hsa_circ_362716,RMVar_hsa_circ_330505,RMVar_hsa_circ_107706,RMVar_hsa_circ_116049,RMVar_hsa_circ_35773,RMVar_hsa_circ_84021,RMVar_hsa_circ_202971,RMVar_hsa_circ_202972,RMVar_hsa_circ_202973,RMVar_hsa_circ_336795,RMVar_hsa_circ_202975,RMVar_hsa_circ_340261,RMVar_hsa_circ_368071,RMVar_hsa_circ_274980,RMVar_hsa_circ_324156,RMVar_hsa_circ_63936,RMVar_hsa_circ_23997,RMVar_hsa_circ_41739,RMVar_hsa_circ_35866,RMVar_hsa_circ_202976,RMVar_hsa_circ_202977,RMVar_hsa_circ_202978,RMVar_hsa_circ_128046,RMVar_hsa_circ_202980,RMVar_hsa_circ_47852,RMVar_hsa_circ_335953,RMVar_hsa_circ_202979,RMVar_hsa_circ_362090,RMVar_hsa_circ_117254,RMVar_hsa_circ_202981,RMVar_hsa_circ_202982,RMVar_hsa_circ_95206,RMVar_hsa_circ_202983,RMVar_hsa_circ_115184,RMVar_hsa_circ_346673,RMVar_hsa_circ_349542,RMVar_hsa_circ_83520,RMVar_hsa_circ_202984,RMVar_hsa_circ_202985 18073 RMVar_ID_18073 Human_SNP_ID_89605571 A-to-I Human chr2 - 121414923 121414923 121414923 AAACAAAGCCGAATGTGGTGGCACATCCCTGTAGTCCCTGCTACTTGGGAGGCTGAGGCAGGCGG AAACAAAGCCGAATGTGGTGGCACATCCCTGTTGTCCCTGCTACTTGGGAGGCTGAGGCAGGCGG T A CLASP1 Ensembl:ENSG00000074054 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1222782321 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8,RMVar_hsa_circ_377955,RMVar_hsa_circ_59229,RMVar_hsa_circ_12677,RMVar_hsa_circ_2088,RMVar_hsa_circ_202968,RMVar_hsa_circ_113267,RMVar_hsa_circ_332151,RMVar_hsa_circ_35606,RMVar_hsa_circ_10357,RMVar_hsa_circ_330505,RMVar_hsa_circ_107706,RMVar_hsa_circ_116049,RMVar_hsa_circ_35773,RMVar_hsa_circ_84021,RMVar_hsa_circ_202972,RMVar_hsa_circ_202973,RMVar_hsa_circ_336795,RMVar_hsa_circ_202975,RMVar_hsa_circ_340261,RMVar_hsa_circ_368071,RMVar_hsa_circ_63936,RMVar_hsa_circ_23997,RMVar_hsa_circ_35866,RMVar_hsa_circ_202976,RMVar_hsa_circ_128046,RMVar_hsa_circ_47852,RMVar_hsa_circ_335953,RMVar_hsa_circ_202979,RMVar_hsa_circ_117254,RMVar_hsa_circ_202981,RMVar_hsa_circ_202982,RMVar_hsa_circ_95206,RMVar_hsa_circ_202983,RMVar_hsa_circ_115184,RMVar_hsa_circ_346673,RMVar_hsa_circ_83520,RMVar_hsa_circ_114717,RMVar_hsa_circ_10540,RMVar_hsa_circ_202984,RMVar_hsa_circ_202985,RMVar_hsa_circ_299890,RMVar_hsa_circ_265366,RMVar_hsa_circ_121076,RMVar_hsa_circ_321693,RMVar_hsa_circ_202988,RMVar_hsa_circ_104441,RMVar_hsa_circ_202989,RMVar_hsa_circ_375940,RMVar_hsa_circ_202987,RMVar_hsa_circ_345459,RMVar_hsa_circ_7864,RMVar_hsa_circ_312789,RMVar_hsa_circ_4834,RMVar_hsa_circ_202990 18074 RMVar_ID_18074 Human_SNP_ID_89609588 A-to-I Human chr2 - 121432370 121432370 121432370 TCCTGCCCGTAATCCCAGAACTTTAGGAGGCCAGGGCGGGTGGATCACTTGAGGTCAGGAGTTGG TCCTGCCCGTAATCCCAGAACTTTAGGAGGCCTGGGCGGGTGGATCACTTGAGGTCAGGAGTTGG T A CLASP1 Ensembl:ENSG00000074054 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs564229012 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8,RMVar_hsa_circ_377955,RMVar_hsa_circ_59229,RMVar_hsa_circ_2088,RMVar_hsa_circ_202968,RMVar_hsa_circ_113267,RMVar_hsa_circ_35606,RMVar_hsa_circ_107706,RMVar_hsa_circ_116049,RMVar_hsa_circ_35773,RMVar_hsa_circ_84021,RMVar_hsa_circ_202972,RMVar_hsa_circ_202973,RMVar_hsa_circ_336795,RMVar_hsa_circ_202975,RMVar_hsa_circ_340261,RMVar_hsa_circ_23997,RMVar_hsa_circ_17053,RMVar_hsa_circ_202976,RMVar_hsa_circ_128046,RMVar_hsa_circ_335953,RMVar_hsa_circ_202979,RMVar_hsa_circ_117254,RMVar_hsa_circ_202981,RMVar_hsa_circ_202982,RMVar_hsa_circ_95206,RMVar_hsa_circ_202983,RMVar_hsa_circ_115184,RMVar_hsa_circ_83520,RMVar_hsa_circ_114717,RMVar_hsa_circ_10540,RMVar_hsa_circ_202984,RMVar_hsa_circ_202985,RMVar_hsa_circ_265366,RMVar_hsa_circ_121076,RMVar_hsa_circ_321693,RMVar_hsa_circ_202988,RMVar_hsa_circ_104441,RMVar_hsa_circ_202989,RMVar_hsa_circ_375940,RMVar_hsa_circ_202987,RMVar_hsa_circ_345459,RMVar_hsa_circ_4834,RMVar_hsa_circ_202990,RMVar_hsa_circ_28609,RMVar_hsa_circ_75407,RMVar_hsa_circ_331480,RMVar_hsa_circ_379049,RMVar_hsa_circ_274232,RMVar_hsa_circ_34935,RMVar_hsa_circ_53008,RMVar_hsa_circ_33243,RMVar_hsa_circ_11930,RMVar_hsa_circ_202991,RMVar_hsa_circ_20514,RMVar_hsa_circ_313605,RMVar_hsa_circ_324495,RMVar_hsa_circ_363288 18075 RMVar_ID_18075 Human_SNP_ID_89611624 A-to-I Human chr2 - 121440583 121440583 121440583 AGGCTCAAGTATCCTCCCACCTCAGCCTTCCAAGTAACTGGGACTACAGGTGTGCAACACCATGC AGGCTCAAGTATCCTCCCACCTCAGCCTTCCACGTAACTGGGACTACAGGTGTGCAACACCATGC T G CLASP1 Ensembl:ENSG00000074054 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1321380145 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8,RMVar_hsa_circ_377955,RMVar_hsa_circ_59229,RMVar_hsa_circ_2088,RMVar_hsa_circ_202968,RMVar_hsa_circ_113267,RMVar_hsa_circ_35606,RMVar_hsa_circ_107706,RMVar_hsa_circ_116049,RMVar_hsa_circ_35773,RMVar_hsa_circ_84021,RMVar_hsa_circ_202972,RMVar_hsa_circ_202973,RMVar_hsa_circ_336795,RMVar_hsa_circ_202975,RMVar_hsa_circ_340261,RMVar_hsa_circ_23997,RMVar_hsa_circ_17053,RMVar_hsa_circ_202976,RMVar_hsa_circ_128046,RMVar_hsa_circ_335953,RMVar_hsa_circ_202979,RMVar_hsa_circ_117254,RMVar_hsa_circ_202981,RMVar_hsa_circ_202982,RMVar_hsa_circ_95206,RMVar_hsa_circ_202983,RMVar_hsa_circ_115184,RMVar_hsa_circ_83520,RMVar_hsa_circ_114717,RMVar_hsa_circ_10540,RMVar_hsa_circ_202984,RMVar_hsa_circ_202985,RMVar_hsa_circ_265366,RMVar_hsa_circ_121076,RMVar_hsa_circ_321693,RMVar_hsa_circ_202988,RMVar_hsa_circ_104441,RMVar_hsa_circ_202989,RMVar_hsa_circ_375940,RMVar_hsa_circ_202987,RMVar_hsa_circ_345459,RMVar_hsa_circ_4834,RMVar_hsa_circ_202990,RMVar_hsa_circ_28609,RMVar_hsa_circ_75407,RMVar_hsa_circ_331480,RMVar_hsa_circ_379049,RMVar_hsa_circ_274232,RMVar_hsa_circ_34935,RMVar_hsa_circ_53008,RMVar_hsa_circ_33243,RMVar_hsa_circ_11930,RMVar_hsa_circ_202991,RMVar_hsa_circ_20514,RMVar_hsa_circ_313605,RMVar_hsa_circ_324495,RMVar_hsa_circ_363288 18076 RMVar_ID_18076 Human_SNP_ID_89625745 A-to-I Human chr2 - 121498486 121498486 121498486 TTGCCTATATTTGGCCAGGTGCAGTGGCTCACACCTGTAATCTCAGCACTTTGCGAGACCGAGAC TTGCCTATATTTGGCCAGGTGCAGTGGCTCACGCCTGTAATCTCAGCACTTTGCGAGACCGAGAC T C CLASP1 Ensembl:ENSG00000074054 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs955288870 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8,RMVar_hsa_circ_202968,RMVar_hsa_circ_113267,RMVar_hsa_circ_107706,RMVar_hsa_circ_35773,RMVar_hsa_circ_202973,RMVar_hsa_circ_128046,RMVar_hsa_circ_202979,RMVar_hsa_circ_117254,RMVar_hsa_circ_202982,RMVar_hsa_circ_83520,RMVar_hsa_circ_114717,RMVar_hsa_circ_202985,RMVar_hsa_circ_121076,RMVar_hsa_circ_202988,RMVar_hsa_circ_104441,RMVar_hsa_circ_202989,RMVar_hsa_circ_202987,RMVar_hsa_circ_75407,RMVar_hsa_circ_33243,RMVar_hsa_circ_318843,RMVar_hsa_circ_113253,RMVar_hsa_circ_202997,RMVar_hsa_circ_32935,RMVar_hsa_circ_84402,RMVar_hsa_circ_203002,RMVar_hsa_circ_27642,RMVar_hsa_circ_31837,RMVar_hsa_circ_335987,RMVar_hsa_circ_373344,RMVar_hsa_circ_203006,RMVar_hsa_circ_203007,RMVar_hsa_circ_101577,RMVar_hsa_circ_203009,RMVar_hsa_circ_108918,RMVar_hsa_circ_98879,RMVar_hsa_circ_33647,RMVar_hsa_circ_203010,RMVar_hsa_circ_203011,RMVar_hsa_circ_53004,RMVar_hsa_circ_318206,RMVar_hsa_circ_203012 18077 RMVar_ID_18077 Human_SNP_ID_89640501 A-to-I Human chr2 - 121556099 121556099 121556099 TGTGCCTGTAATTCCAGCTACTTGGAAGGCTGAGGCCGAGAATTTGCTTGAACCTGGGAGGCAGA TGTGCCTGTAATTCCAGCTACTTGGAAGGCTGCGGCCGAGAATTTGCTTGAACCTGGGAGGCAGA T G CLASP1 Ensembl:ENSG00000074054 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1024028206 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8,RMVar_hsa_circ_107706,RMVar_hsa_circ_202973,RMVar_hsa_circ_128046,RMVar_hsa_circ_202979,RMVar_hsa_circ_117254,RMVar_hsa_circ_202982,RMVar_hsa_circ_83520,RMVar_hsa_circ_202985,RMVar_hsa_circ_121076,RMVar_hsa_circ_202987,RMVar_hsa_circ_113253,RMVar_hsa_circ_202997,RMVar_hsa_circ_84402,RMVar_hsa_circ_203002,RMVar_hsa_circ_373344,RMVar_hsa_circ_203007,RMVar_hsa_circ_302647,RMVar_hsa_circ_120025,RMVar_hsa_circ_203014,RMVar_hsa_circ_203015,RMVar_hsa_circ_359257,RMVar_hsa_circ_68211,RMVar_hsa_circ_98014,RMVar_hsa_circ_203019 18078 RMVar_ID_18078 Human_SNP_ID_89644166 A-to-I Human chr2 - 121572699 121572699 121572699 TAGAAACGTGGTTTCACCATGTTGCCCAGGCTAGTCTCAAACTTCTGAGCTCAGGTGATCTGCCC TAGAAACGTGGTTTCACCATGTTGCCCAGGCTGGTCTCAAACTTCTGAGCTCAGGTGATCTGCCC T C CLASP1 Ensembl:ENSG00000074054 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1279043356 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8,RMVar_hsa_circ_107706,RMVar_hsa_circ_202973,RMVar_hsa_circ_128046,RMVar_hsa_circ_202979,RMVar_hsa_circ_117254,RMVar_hsa_circ_202982,RMVar_hsa_circ_83520,RMVar_hsa_circ_202985,RMVar_hsa_circ_121076,RMVar_hsa_circ_202987,RMVar_hsa_circ_113253,RMVar_hsa_circ_202997,RMVar_hsa_circ_84402,RMVar_hsa_circ_203002,RMVar_hsa_circ_373344,RMVar_hsa_circ_203007,RMVar_hsa_circ_302647,RMVar_hsa_circ_120025,RMVar_hsa_circ_203014,RMVar_hsa_circ_203015,RMVar_hsa_circ_359257,RMVar_hsa_circ_68211,RMVar_hsa_circ_98014,RMVar_hsa_circ_203019 18079 RMVar_ID_18079 Human_SNP_ID_89649610 A-to-I Human chr2 - 121594042 121594042 121594042 CACCCGCCTCGGCCTCCCAAAGTGTTGGGATTACAGGCGTGAGCCACCGCGCCAGGCCTTTTTTT CACCCGCCTCGGCCTCCCAAAGTGTTGGGATTGCAGGCGTGAGCCACCGCGCCAGGCCTTTTTTT T C CLASP1 Ensembl:ENSG00000074054 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1465866272 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8,RMVar_hsa_circ_107706,RMVar_hsa_circ_202973,RMVar_hsa_circ_128046,RMVar_hsa_circ_202979,RMVar_hsa_circ_117254,RMVar_hsa_circ_202982,RMVar_hsa_circ_83520,RMVar_hsa_circ_202985,RMVar_hsa_circ_121076,RMVar_hsa_circ_202987,RMVar_hsa_circ_113253,RMVar_hsa_circ_202997,RMVar_hsa_circ_84402,RMVar_hsa_circ_203002,RMVar_hsa_circ_373344,RMVar_hsa_circ_203007,RMVar_hsa_circ_302647,RMVar_hsa_circ_120025,RMVar_hsa_circ_203014,RMVar_hsa_circ_203015,RMVar_hsa_circ_359257,RMVar_hsa_circ_68211,RMVar_hsa_circ_98014,RMVar_hsa_circ_203019 18080 RMVar_ID_18080 Human_SNP_ID_89650892 A-to-I Human chr2 - 121599403 121599403 121599403 TTGTATTTTTAGTAGAGACAGGGTTTTACCATATTGGCCAGGCTGGTCTTGAACTCCTGACTGCC TTGTATTTTTAGTAGAGACAGGGTTTTACCATGTTGGCCAGGCTGGTCTTGAACTCCTGACTGCC T C CLASP1 Ensembl:ENSG00000074054 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1396825304 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8,RMVar_hsa_circ_107706,RMVar_hsa_circ_202973,RMVar_hsa_circ_128046,RMVar_hsa_circ_202979,RMVar_hsa_circ_117254,RMVar_hsa_circ_202982,RMVar_hsa_circ_83520,RMVar_hsa_circ_202985,RMVar_hsa_circ_121076,RMVar_hsa_circ_202987,RMVar_hsa_circ_113253,RMVar_hsa_circ_202997,RMVar_hsa_circ_84402,RMVar_hsa_circ_203002,RMVar_hsa_circ_373344,RMVar_hsa_circ_203007,RMVar_hsa_circ_302647,RMVar_hsa_circ_120025,RMVar_hsa_circ_203014,RMVar_hsa_circ_203015,RMVar_hsa_circ_359257,RMVar_hsa_circ_68211,RMVar_hsa_circ_98014,RMVar_hsa_circ_203019 18081 RMVar_ID_18081 Human_SNP_ID_89659016 A-to-I Human chr2 - 121631987 121631987 121631987 GCTGGAGTGCAGTGGCGTGATCTCGGCTCACTACAGCCTCCGCCTCCTGGGTTCAAGCAGTTCTC GCTGGAGTGCAGTGGCGTGATCTCGGCTCACTGCAGCCTCCGCCTCCTGGGTTCAAGCAGTTCTC T C CLASP1 Ensembl:ENSG00000074054 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1231268537 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120025,RMVar_hsa_circ_203015 18082 RMVar_ID_18082 Human_SNP_ID_89664061 A-to-I Human chr2 + 121651909 121651909 121651909 AAAACCCTGTCTCTACTAAAAATACAAAAATTAGCCGGGTACGGTGGCACACACCTGTAATCCCA AAAACCCTGTCTCTACTAAAAATACAAAAATTGGCCGGGTACGGTGGCACACACCTGTAATCCCA A G NIFK-AS1 Ensembl:ENSG00000236859 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1173287487 Functional Loss SNV dbSNP153 33..33 33 - - - 18083 RMVar_ID_18083 Human_SNP_ID_89664178 A-to-I Human chr2 + 121652378 121652378 121652378 TTTAGTAGAGGCGGGGTTTCACCATGTTGGCCAGGATGGTCTCGATCTCTTGACCTCGTGATCCA TTTAGTAGAGGCGGGGTTTCACCATGTTGGCCTGGATGGTCTCGATCTCTTGACCTCGTGATCCA A T NIFK-AS1 Ensembl:ENSG00000236859 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs572718215 Functional Loss SNV dbSNP153 33..33 33 - - - 18084 RMVar_ID_18084 Human_SNP_ID_91094810 A-to-I Human chr2 - 127257843 127257843 127257843 CTGAGACAGTAAGCGATCTGTAAACATTATTAAAAATGATGTATTAAATTTATGTAAGTCTTATA CTGAGACAGTAAGCGATCTGTAAACATTATTACAAATGATGTATTAAATTTATGTAAGTCTTATA T G ERCC3 Ensembl:ENSG00000163161 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs186365327 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107369,RMVar_hsa_circ_203054 18085 RMVar_ID_18085 Human_SNP_ID_91095825 A-to-I Human chr2 - 127262290 127262290 127262290 TGGAGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTCCTGACCTTGAGTGATCCACGCCCACCT TGGAGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTTGAGTGATCCACGCCCACCT T C ERCC3 Ensembl:ENSG00000163161 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1422243369 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51035,RMVar_hsa_circ_107369,RMVar_hsa_circ_203054 18086 RMVar_ID_18086 Human_SNP_ID_91095836 A-to-I Human chr2 - 127262330 127262330 127262330 AGCCACCACGCCTGGCTAATTTTTCTATTTTTAGTAGAGATGGAGTTTCACCATGTTGGCCAGGC AGCCACCACGCCTGGCTAATTTTTCTATTTTTGGTAGAGATGGAGTTTCACCATGTTGGCCAGGC T C ERCC3 Ensembl:ENSG00000163161 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1168502599 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51035,RMVar_hsa_circ_107369,RMVar_hsa_circ_203054 18087 RMVar_ID_18087 Human_SNP_ID_91095850 A-to-I Human chr2 - 127262371 127262371 127262371 CTCCTGCCTCAGCCTCCCGCGTAGCTGGAATTACAGGCATGAGCCACCACGCCTGGCTAATTTTT CTCCTGCCTCAGCCTCCCGCGTAGCTGGAATTGCAGGCATGAGCCACCACGCCTGGCTAATTTTT T C ERCC3 Ensembl:ENSG00000163161 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1454883702 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51035,RMVar_hsa_circ_107369,RMVar_hsa_circ_203054 18088 RMVar_ID_18088 Human_SNP_ID_91096327 A-to-I Human chr2 - 127264419 127264419 127264419 TCTTGTTGCCCAGGCTGGAGTGCAATGGTGCAATCTTGGCTCACTGCAACCTCTGCTTCCCAGAT TCTTGTTGCCCAGGCTGGAGTGCAATGGTGCAGTCTTGGCTCACTGCAACCTCTGCTTCCCAGAT T C ERCC3 Ensembl:ENSG00000163161 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 29129909,30559470 RNA-Seq:(High) rs986434940 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51035,RMVar_hsa_circ_107369,RMVar_hsa_circ_203054 18089 RMVar_ID_18089 Human_SNP_ID_91097740 A-to-I Human chr2 - 127269898 127269898 127269898 TCACCTGCCTCAGCCTCCCGAGTACCCGGACTACAGGCGTGCACCACCACGTCCAGCTAATTTTT TCACCTGCCTCAGCCTCCCGAGTACCCGGACTGCAGGCGTGCACCACCACGTCCAGCTAATTTTT T C ERCC3 Ensembl:ENSG00000163161 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560513303 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51035,RMVar_hsa_circ_107369,RMVar_hsa_circ_203054 18090 RMVar_ID_18090 Human_SNP_ID_91097771 A-to-I Human chr2 - 127270015 127270015 127270015 ATTGATTGATTGATTGATTGATTGATTGAGATAGAGTCTTATTCTGTCACCCAGGCTGGAGTGCA ATTGATTGATTGATTGATTGATTGATTGAGATGGAGTCTTATTCTGTCACCCAGGCTGGAGTGCA T C ERCC3 Ensembl:ENSG00000163161 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1381077128 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51035,RMVar_hsa_circ_107369,RMVar_hsa_circ_203054 18091 RMVar_ID_18091 Human_SNP_ID_91101320 A-to-I Human chr2 - 127284760 127284760 127284760 AGGATCACTTGAACCTGGGAGGTTGAGGCTGCAGTGAACCATGATTGTGCAACTGTACTCCAGCA AGGATCACTTGAACCTGGGAGGTTGAGGCTGCGGTGAACCATGATTGTGCAACTGTACTCCAGCA T C ERCC3 Ensembl:ENSG00000163161 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1310294663 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51035,RMVar_hsa_circ_203059,RMVar_hsa_circ_203057,RMVar_hsa_circ_303971,RMVar_hsa_circ_335117,RMVar_hsa_circ_344793,RMVar_hsa_circ_269462,RMVar_hsa_circ_203056,RMVar_hsa_circ_310525,RMVar_hsa_circ_376252,RMVar_hsa_circ_203062,RMVar_hsa_circ_304714,RMVar_hsa_circ_203058 18092 RMVar_ID_18092 Human_SNP_ID_91102999 A-to-I Human chr2 - 127290960 127290960 127290960 CTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTATAGGCGCCCGTCACCATGCCCGGCTAATTTTT CTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTGTAGGCGCCCGTCACCATGCCCGGCTAATTTTT T C ERCC3 Ensembl:ENSG00000163161 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1396675660 Functional Loss SNV dbSNP153 33..33 33 - - - 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_94418,RMVar_hsa_circ_301574,RMVar_hsa_circ_203069 18093 RMVar_ID_18093 Human_SNP_ID_91103033 A-to-I Human chr2 - 127291078 127291077 127291079 ACTGGCAAATTTTTTTTTTCTTTTTTTTTGAGACGGAGTCTTGCTCTGTCGCCCAGGCTGGATAG ACTGGCAAATTTTTTTTTTCTTTTTTTTTGA__CGGAGTCTTGCTCTGTCGCCCAGGCTGGATAG GTC G ERCC3 Ensembl:ENSG00000163161 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1338807691 Functional Loss DEL dbSNP153 32..33 33 - - - 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_94418,RMVar_hsa_circ_301574,RMVar_hsa_circ_203069 18094 RMVar_ID_18094 Human_SNP_ID_91103245 A-to-I Human chr2 - 127292055 127292055 127292055 TCATGTGAGTACACAATGGGAAGGTGGTCCATAGACAAGAGCCTTCACCAGAAACTGAATCGGCT TCATGTGAGTACACAATGGGAAGGTGGTCCATGGACAAGAGCCTTCACCAGAAACTGAATCGGCT T C ERCC3 Ensembl:ENSG00000163161 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4150407 Functional Loss SNV dbSNP153,EGP 33..33 33 - - - GWAS_ID_1611,GWAS_ID_1612,GWAS_ID_1613,GWAS_ID_1614,GWAS_ID_1615,GWAS_ID_1616,GWAS_ID_1617,GWAS_ID_1618,GWAS_ID_1619,GWAS_ID_1620,GWAS_ID_1621,GWAS_ID_1622,GWAS_ID_1623,GWAS_ID_1624,GWAS_ID_1625,GWAS_ID_1626,GWAS_ID_1627 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_94418,RMVar_hsa_circ_301574,RMVar_hsa_circ_203069 18095 RMVar_ID_18095 Human_SNP_ID_91112262 A-to-I Human chr2 - 127328087 127328087 127328087 TATTTTTAGTAGAGATGGGGTTTCAGCCTGTTAGCCAGATTGGTCTCGAACTCCTGACCTCATGT TATTTTTAGTAGAGATGGGGTTTCAGCCTGTTCGCCAGATTGGTCTCGAACTCCTGACCTCATGT T G MAP3K2 Ensembl:ENSG00000169967 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs898878247 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_347921,RMVar_hsa_circ_364114,RMVar_hsa_circ_70047,RMVar_hsa_circ_287394,RMVar_hsa_circ_22099,RMVar_hsa_circ_53630,RMVar_hsa_circ_288762,RMVar_hsa_circ_203072,RMVar_hsa_circ_27373,RMVar_hsa_circ_317842,RMVar_hsa_circ_268052,RMVar_hsa_circ_203074 18096 RMVar_ID_18096 Human_SNP_ID_91112288 A-to-I Human chr2 - 127328192 127328192 127328192 CAGCTAACTGTAACCGCTGCCTCCTGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCTGAATAACT CAGCTAACTGTAACCGCTGCCTCCTGGGTTCAGGTGATTCTCCTGCCTCAGCCTCCTGAATAACT T C MAP3K2 Ensembl:ENSG00000169967 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs977515242 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_347921,RMVar_hsa_circ_364114,RMVar_hsa_circ_70047,RMVar_hsa_circ_287394,RMVar_hsa_circ_22099,RMVar_hsa_circ_53630,RMVar_hsa_circ_288762,RMVar_hsa_circ_203072,RMVar_hsa_circ_27373,RMVar_hsa_circ_317842,RMVar_hsa_circ_268052,RMVar_hsa_circ_203074 18097 RMVar_ID_18097 Human_SNP_ID_91113857 A-to-I Human chr2 - 127334652 127334652 127334652 ATCACCTGAGGCCGGGAGTTCAAGACTAGCCTAGGCAACATAGCCAGACTCCATCTCTACAAAAA ATCACCTGAGGCCGGGAGTTCAAGACTAGCCTGGGCAACATAGCCAGACTCCATCTCTACAAAAA T C MAP3K2 Ensembl:ENSG00000169967 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924296435 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_364114,RMVar_hsa_circ_203076,RMVar_hsa_circ_22099,RMVar_hsa_circ_53630,RMVar_hsa_circ_27373,RMVar_hsa_circ_277046,RMVar_hsa_circ_268052,RMVar_hsa_circ_333295,RMVar_hsa_circ_203078,RMVar_hsa_circ_272772,RMVar_hsa_circ_203077 18098 RMVar_ID_18098 Human_SNP_ID_91121377 A-to-I Human chr2 - 127363768 127363768 127363768 CCTGTAGTCTTAGCTACTCAGGAGGCTGAGGTAGGAGGATTGCTTGAGCCAGGCTAGGTGACAGA CCTGTAGTCTTAGCTACTCAGGAGGCTGAGGTGGGAGGATTGCTTGAGCCAGGCTAGGTGACAGA T C MAP3K2 Ensembl:ENSG00000169967 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971852031 Functional Loss SNV dbSNP153 33..33 33 - - - 18099 RMVar_ID_18099 Human_SNP_ID_91122542 A-to-I Human chr2 - 127368240 127368240 127368240 TCGGCTCACTGCAGCCTCTGCCTTCTGGGTTCAAGTGATTCTTGTGCCTCAGCCTCCCAAGTACC TCGGCTCACTGCAGCCTCTGCCTTCTGGGTTCGAGTGATTCTTGTGCCTCAGCCTCCCAAGTACC T C MAP3K2 Ensembl:ENSG00000169967 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs527315787 Functional Loss SNV dbSNP153 33..33 33 - - - 18100 RMVar_ID_18100 Human_SNP_ID_91124852 A-to-I Human chr2 - 127376918 127376918 127376918 TAGCTGGGACTACAGGCACACCATTATACCCAACTAATTTTTAAATTTTTGTAGAGGTAGGGTCT TAGCTGGGACTACAGGCACACCATTATACCCAGCTAATTTTTAAATTTTTGTAGAGGTAGGGTCT T C MAP3K2 Ensembl:ENSG00000169967 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1438515933 Functional Loss SNV dbSNP153 33..33 33 - - - 18101 RMVar_ID_18101 Human_SNP_ID_91124881 A-to-I Human chr2 - 127377042 127377042 127377042 TCTTTTTTTTTTTTGAGACAGGATCTCGCTCTATCATTCAGGCTGGAGTGCAGTGTCAGGATCAC TCTTTTTTTTTTTTGAGACAGGATCTCGCTCTGTCATTCAGGCTGGAGTGCAGTGTCAGGATCAC T C MAP3K2 Ensembl:ENSG00000169967 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs901610405 Functional Loss SNV dbSNP153 33..33 33 - - - 18102 RMVar_ID_18102 Human_SNP_ID_91159786 A-to-I Human chr2 - 127518467 127518467 127518467 CACTGTCGCCCGGGCTGGAGTGTAGTGGCACAATCACAGCTCACTGCAGCCTCAACCTCCCACGC CACTGTCGCCCGGGCTGGAGTGTAGTGGCACAGTCACAGCTCACTGCAGCCTCAACCTCCCACGC T C IWS1 Ensembl:ENSG00000163166 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1307896741 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_353977,RMVar_hsa_circ_20114,RMVar_hsa_circ_71333,RMVar_hsa_circ_365764,RMVar_hsa_circ_64539,RMVar_hsa_circ_353008,RMVar_hsa_circ_203093 18103 RMVar_ID_18103 Human_SNP_ID_91159801 A-to-I Human chr2 - 127518500 127518500 127518500 CTTTTTCTTTTTCTTTTTTGAGGCAGAATCTTACACTGTCGCCCGGGCTGGAGTGTAGTGGCACA CTTTTTCTTTTTCTTTTTTGAGGCAGAATCTTGCACTGTCGCCCGGGCTGGAGTGTAGTGGCACA T C IWS1 Ensembl:ENSG00000163166 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1203328266 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_353977,RMVar_hsa_circ_20114,RMVar_hsa_circ_71333,RMVar_hsa_circ_365764,RMVar_hsa_circ_64539,RMVar_hsa_circ_353008,RMVar_hsa_circ_203093 18104 RMVar_ID_18104 Human_SNP_ID_91212578 A-to-I Human chr2 - 127711342 127711342 127711342 CGGCTCACTGCAGCCTCCACCTCCTGGGTTCAAGCGATTCTTGTGCTTCAGCCTCCCGAGTAGCT CGGCTCACTGCAGCCTCCACCTCCTGGGTTCAGGCGATTCTTGTGCTTCAGCCTCCCGAGTAGCT T C WDR33 Ensembl:ENSG00000136709 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1045189429 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9971,RMVar_hsa_circ_25014,RMVar_hsa_circ_53061 18105 RMVar_ID_18105 Human_SNP_ID_91212592 A-to-I Human chr2 - 127711381 127711381 127711381 TTGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCATGATCTCGGCTCACTGCAGCCTCCACCTCCTG TTGCTTTGTCGCTCAGGCTGGAGTGCAGTGGCGTGATCTCGGCTCACTGCAGCCTCCACCTCCTG T C WDR33 Ensembl:ENSG00000136709 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1382605081 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9971,RMVar_hsa_circ_25014,RMVar_hsa_circ_53061 18106 RMVar_ID_18106 Human_SNP_ID_91212960 A-to-I Human chr2 - 127711888 127711888 127711888 CGTGCCTGTAATCCCAGCTACTCGGAAGGCTGAGGCAGGAGAATCGTCTGAATCTGGGAGGCAGA CGTGCCTGTAATCCCAGCTACTCGGAAGGCTGGGGCAGGAGAATCGTCTGAATCTGGGAGGCAGA T C WDR33 Ensembl:ENSG00000136709 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1264176691 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9971,RMVar_hsa_circ_25014,RMVar_hsa_circ_53061 18107 RMVar_ID_18107 Human_SNP_ID_91213006 A-to-I Human chr2 - 127712053 127712053 127712053 GAATAGATGGTTAAGGCCGGGCACAGTGGCTCACGCTTGTAATCCCAGCACTTTGGGAGGCCGAG GAATAGATGGTTAAGGCCGGGCACAGTGGCTCGCGCTTGTAATCCCAGCACTTTGGGAGGCCGAG T C WDR33 Ensembl:ENSG00000136709 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1180551755 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9971,RMVar_hsa_circ_25014,RMVar_hsa_circ_53061 18108 RMVar_ID_18108 Human_SNP_ID_91213192 A-to-I Human chr2 - 127712823 127712823 127712823 CTGAGGCCAGGAGGCTGCAGTGAGTTATGATTATGCCATTGCACTTCAGCCTGGGCTACAGAGCA CTGAGGCCAGGAGGCTGCAGTGAGTTATGATTTTGCCATTGCACTTCAGCCTGGGCTACAGAGCA T A WDR33 Ensembl:ENSG00000136709 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs562920598 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9971,RMVar_hsa_circ_25014,RMVar_hsa_circ_53061 18109 RMVar_ID_18109 Human_SNP_ID_91213204 A-to-I Human chr2 - 127712901 127712901 127712901 AAAATTTTTTAATTAGCTGGGTTTGGTGGTGCATGCCTGTAGTCCTAGCTACTCAGGAAGCTGAG AAAATTTTTTAATTAGCTGGGTTTGGTGGTGCGTGCCTGTAGTCCTAGCTACTCAGGAAGCTGAG T C WDR33 Ensembl:ENSG00000136709 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1220831907 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9971,RMVar_hsa_circ_25014,RMVar_hsa_circ_53061 18110 RMVar_ID_18110 Human_SNP_ID_91217618 A-to-I Human chr2 - 127731903 127731903 127731903 TTAAGTTTTTCTTCTAGAGACAGGGTCTCACTATGTTGCCCAGGCTGATCTCTACCTCCTGGACT TTAAGTTTTTCTTCTAGAGACAGGGTCTCACTGTGTTGCCCAGGCTGATCTCTACCTCCTGGACT T C WDR33 Ensembl:ENSG00000136709 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1309689278 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23823531 RMVar_hsa_circ_3861,RMVar_hsa_circ_53061,RMVar_hsa_circ_28002,RMVar_hsa_circ_266072,RMVar_hsa_circ_89884,RMVar_hsa_circ_355349,RMVar_hsa_circ_123607,RMVar_hsa_circ_203097,RMVar_hsa_circ_203098,RMVar_hsa_circ_121021,RMVar_hsa_circ_115922,RMVar_hsa_circ_203101,RMVar_hsa_circ_203102,RMVar_hsa_circ_24987 18111 RMVar_ID_18111 Human_SNP_ID_91217804 A-to-I Human chr2 - 127732460 127732460 127732460 AAAATTACCTGGACGTGATAGTGCATGCCTGTAGTCCCAGCTACCGGGGAGGCTGAGGTAGGAGG AAAATTACCTGGACGTGATAGTGCATGCCTGTGGTCCCAGCTACCGGGGAGGCTGAGGTAGGAGG T C WDR33 Ensembl:ENSG00000136709 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1436381418 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3861,RMVar_hsa_circ_53061,RMVar_hsa_circ_28002,RMVar_hsa_circ_266072,RMVar_hsa_circ_89884,RMVar_hsa_circ_355349,RMVar_hsa_circ_123607,RMVar_hsa_circ_203097,RMVar_hsa_circ_203098,RMVar_hsa_circ_121021,RMVar_hsa_circ_115922,RMVar_hsa_circ_203101,RMVar_hsa_circ_203102,RMVar_hsa_circ_24987 18112 RMVar_ID_18112 Human_SNP_ID_91221515 A-to-I Human chr2 - 127748837 127748837 127748837 AGGAGGCCCTGTTAGGAGGATCACTTGAGCCCAGGAGATCGAGACAGTAATGAGCCATGCACCAC AGGAGGCCCTGTTAGGAGGATCACTTGAGCCCGGGAGATCGAGACAGTAATGAGCCATGCACCAC T C WDR33 Ensembl:ENSG00000136709 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs939895370 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6821609,Human_RBP_ID_13603233,Human_RBP_ID_22813488,Human_RBP_ID_24560593 RMVar_hsa_circ_3861,RMVar_hsa_circ_53061,RMVar_hsa_circ_28002,RMVar_hsa_circ_266072,RMVar_hsa_circ_89884,RMVar_hsa_circ_355349,RMVar_hsa_circ_123607,RMVar_hsa_circ_203097,RMVar_hsa_circ_203098,RMVar_hsa_circ_121021,RMVar_hsa_circ_115922,RMVar_hsa_circ_86023,RMVar_hsa_circ_203101,RMVar_hsa_circ_203102,RMVar_hsa_circ_24987,RMVar_hsa_circ_203103 18113 RMVar_ID_18113 Human_SNP_ID_91221861 A-to-I Human chr2 - 127750092 127750092 127750092 TGAACCTGGGAAATCTGAGGCTGCAGTGAGCCAAGATTTCGCCACTGCACTCAAGCCTGGGTGGC TGAACCTGGGAAATCTGAGGCTGCAGTGAGCCGAGATTTCGCCACTGCACTCAAGCCTGGGTGGC T C WDR33 Ensembl:ENSG00000136709 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10172438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6821636,Human_RBP_ID_13603294,Human_RBP_ID_17569876,Human_RBP_ID_25460183 RMVar_hsa_circ_3861,RMVar_hsa_circ_53061,RMVar_hsa_circ_28002,RMVar_hsa_circ_266072,RMVar_hsa_circ_89884,RMVar_hsa_circ_355349,RMVar_hsa_circ_123607,RMVar_hsa_circ_203097,RMVar_hsa_circ_203098,RMVar_hsa_circ_121021,RMVar_hsa_circ_115922,RMVar_hsa_circ_86023,RMVar_hsa_circ_203101,RMVar_hsa_circ_203102,RMVar_hsa_circ_24987,RMVar_hsa_circ_203103 18114 RMVar_ID_18114 Human_SNP_ID_91221920 A-to-I Human chr2 - 127750279 127750279 127750279 TCATGCCAGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGCAGATCACTTGAGCCCAGGAGTTTG TCATGCCAGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGCAGATCACTTGAGCCCAGGAGTTTG T C WDR33 Ensembl:ENSG00000136709 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1453736662 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3861,RMVar_hsa_circ_53061,RMVar_hsa_circ_28002,RMVar_hsa_circ_266072,RMVar_hsa_circ_89884,RMVar_hsa_circ_355349,RMVar_hsa_circ_123607,RMVar_hsa_circ_203097,RMVar_hsa_circ_203098,RMVar_hsa_circ_121021,RMVar_hsa_circ_115922,RMVar_hsa_circ_86023,RMVar_hsa_circ_203101,RMVar_hsa_circ_203102,RMVar_hsa_circ_24987,RMVar_hsa_circ_203103 18115 RMVar_ID_18115 Human_SNP_ID_91221982 A-to-I Human chr2 - 127750519 127750519 127750519 CCTCAGCCTCTCGGGTAGCTGGGATTATAGGCACGTGCCACCATGCCTGGCTAATTTTTGTATTT CCTCAGCCTCTCGGGTAGCTGGGATTATAGGCCCGTGCCACCATGCCTGGCTAATTTTTGTATTT T G WDR33 Ensembl:ENSG00000136709 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1285461555 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3861,RMVar_hsa_circ_53061,RMVar_hsa_circ_28002,RMVar_hsa_circ_266072,RMVar_hsa_circ_89884,RMVar_hsa_circ_355349,RMVar_hsa_circ_123607,RMVar_hsa_circ_203097,RMVar_hsa_circ_203098,RMVar_hsa_circ_121021,RMVar_hsa_circ_115922,RMVar_hsa_circ_86023,RMVar_hsa_circ_203101,RMVar_hsa_circ_203102,RMVar_hsa_circ_24987,RMVar_hsa_circ_203103 18116 RMVar_ID_18116 Human_SNP_ID_91223853 A-to-I Human chr2 - 127756982 127756981 127756982 ACCTCCACCTTGCAGGTTCAAGCAATTCTCCCACCTCAGCCTCCCTGGTAGCTGGGACTACAGGC ACCTCCACCTTGCAGGTTCAAGCAATTCTCCC_CCTCAGCCTCCCTGGTAGCTGGGACTACAGGC GT G WDR33 Ensembl:ENSG00000136709 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs773768945 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_3861,RMVar_hsa_circ_53061,RMVar_hsa_circ_28002,RMVar_hsa_circ_266072,RMVar_hsa_circ_89884,RMVar_hsa_circ_355349,RMVar_hsa_circ_123607,RMVar_hsa_circ_203097,RMVar_hsa_circ_203098,RMVar_hsa_circ_121021,RMVar_hsa_circ_115922,RMVar_hsa_circ_86023,RMVar_hsa_circ_203101,RMVar_hsa_circ_203102,RMVar_hsa_circ_24987,RMVar_hsa_circ_203104,RMVar_hsa_circ_203103 18117 RMVar_ID_18117 Human_SNP_ID_91223854 A-to-I Human chr2 - 127756982 127756982 127756982 ACCTCCACCTTGCAGGTTCAAGCAATTCTCCCACCTCAGCCTCCCTGGTAGCTGGGACTACAGGC ACCTCCACCTTGCAGGTTCAAGCAATTCTCCCGCCTCAGCCTCCCTGGTAGCTGGGACTACAGGC T C WDR33 Ensembl:ENSG00000136709 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1267142677 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3861,RMVar_hsa_circ_53061,RMVar_hsa_circ_28002,RMVar_hsa_circ_266072,RMVar_hsa_circ_89884,RMVar_hsa_circ_355349,RMVar_hsa_circ_123607,RMVar_hsa_circ_203097,RMVar_hsa_circ_203098,RMVar_hsa_circ_121021,RMVar_hsa_circ_115922,RMVar_hsa_circ_86023,RMVar_hsa_circ_203101,RMVar_hsa_circ_203102,RMVar_hsa_circ_24987,RMVar_hsa_circ_203104,RMVar_hsa_circ_203103 18118 RMVar_ID_18118 Human_SNP_ID_91224890 A-to-I Human chr2 - 127761384 127761384 127761384 CATCCTGGCTAACACCATGAAACTCTGTCTCTACTGAAAATACAAAAAATTAGCTGGGTGTCGTG CATCCTGGCTAACACCATGAAACTCTGTCTCTGCTGAAAATACAAAAAATTAGCTGGGTGTCGTG T C WDR33 Ensembl:ENSG00000136709 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs772625184 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3861,RMVar_hsa_circ_53061,RMVar_hsa_circ_28002,RMVar_hsa_circ_266072,RMVar_hsa_circ_89884,RMVar_hsa_circ_355349,RMVar_hsa_circ_123607,RMVar_hsa_circ_203097,RMVar_hsa_circ_203098,RMVar_hsa_circ_121021,RMVar_hsa_circ_115922,RMVar_hsa_circ_86023,RMVar_hsa_circ_203101,RMVar_hsa_circ_203102,RMVar_hsa_circ_24987,RMVar_hsa_circ_203104,RMVar_hsa_circ_203103 18119 RMVar_ID_18119 Human_SNP_ID_91228935 A-to-I Human chr2 - 127777749 127777748 127777750 AAATTAGCTGAGCCCAGGTGGCACACATGTGTAGTCCCACATACTTGGGAGGCTGAGACAGGAGA AAATTAGCTGAGCCCAGGTGGCACACATGTG__GTCCCACATACTTGGGAGGCTGAGACAGGAGA CTA C WDR33 Ensembl:ENSG00000136709 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1188373184 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_13604453 18120 RMVar_ID_18120 Human_SNP_ID_91229036 A-to-I Human chr2 - 127778129 127778129 127778129 ACCCAGCCAATAATTTTTTAAAATTTTTTTGCAGAGATGGGGGTCTTGCTATTCTGCCTAGGCTT ACCCAGCCAATAATTTTTTAAAATTTTTTTGCTGAGATGGGGGTCTTGCTATTCTGCCTAGGCTT T A WDR33 Ensembl:ENSG00000136709 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946020672 Functional Loss SNV dbSNP153 33..33 33 - - - 18121 RMVar_ID_18121 Human_SNP_ID_91229112 A-to-I Human chr2 - 127778406 127778406 127778406 TTGAGATGGAGTCTTGCTCTGTTGCCCAGGCTAGAGTTCAGTGGCATGATCTTGGCTCATTGCAG TTGAGATGGAGTCTTGCTCTGTTGCCCAGGCTGGAGTTCAGTGGCATGATCTTGGCTCATTGCAG T C WDR33 Ensembl:ENSG00000136709 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1314284046 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569879 18122 RMVar_ID_18122 Human_SNP_ID_91230777 A-to-I Human chr2 - 127784461 127784461 127784461 GAAGATGACCTGAGCCTACATGGTCAAGCTGCAGGGTGCCGTGATTGCACCACTGCACTCCAGCC GAAGATGACCTGAGCCTACATGGTCAAGCTGCGGGGTGCCGTGATTGCACCACTGCACTCCAGCC T C WDR33 Ensembl:ENSG00000136709 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs980617342 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13604683 18123 RMVar_ID_18123 Human_SNP_ID_91231180 A-to-I Human chr2 - 127786126 127786126 127786126 AGGAGGCTGAGGTGAGAGGATTGTTTGAGCCTAGGAGGTTTAAGCTGCAGTGAGCTGTGATTGTG AGGAGGCTGAGGTGAGAGGATTGTTTGAGCCTGGGAGGTTTAAGCTGCAGTGAGCTGTGATTGTG T C WDR33 Ensembl:ENSG00000136709 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285037025 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6822039,Human_RBP_ID_13604742 18124 RMVar_ID_18124 Human_SNP_ID_91231280 A-to-I Human chr2 - 127786500 127786500 127786500 GTTTGTATTTTTAGTAGAGACAAAGTTTTGCCATGTTGACTGAGCTGGTCTTGAACTCCTGGCCT GTTTGTATTTTTAGTAGAGACAAAGTTTTGCCGTGTTGACTGAGCTGGTCTTGAACTCCTGGCCT T C WDR33 Ensembl:ENSG00000136709 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs546293932 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2585010,Human_RBP_ID_17570454 18125 RMVar_ID_18125 Human_SNP_ID_91231301 A-to-I Human chr2 - 127786571 127786571 127786571 TCAAGCAATTCTCATGCTGTAGCCTCCTGTGTAGCTGGGATCACAGGTGTGCACCACCATGCCCA TCAAGCAATTCTCATGCTGTAGCCTCCTGTGTGGCTGGGATCACAGGTGTGCACCACCATGCCCA T C WDR33 Ensembl:ENSG00000136709 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1371289123 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8500585,Human_RBP_ID_13604754 18126 RMVar_ID_18126 Human_SNP_ID_91233736 A-to-I Human chr2 - 127794650 127794650 127794650 TTTGTATTTTTAGTAGAGACAGGGGTTTCACCATATTGGCCGGGTTGGTCTTGAACTCCTGATCT TTTGTATTTTTAGTAGAGACAGGGGTTTCACCGTATTGGCCGGGTTGGTCTTGAACTCCTGATCT T C WDR33 Ensembl:ENSG00000136709 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs894798475 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13604918 18127 RMVar_ID_18127 Human_SNP_ID_91233737 A-to-I Human chr2 - 127794650 127794650 127794650 TTTGTATTTTTAGTAGAGACAGGGGTTTCACCATATTGGCCGGGTTGGTCTTGAACTCCTGATCT TTTGTATTTTTAGTAGAGACAGGGGTTTCACCCTATTGGCCGGGTTGGTCTTGAACTCCTGATCT T G WDR33 Ensembl:ENSG00000136709 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs894798475 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13604918 18128 RMVar_ID_18128 Human_SNP_ID_91234293 A-to-I Human chr2 - 127796554 127796554 127796554 CTGGGAAAGAGCCCAAGAAATGATTTTTTTGTAGAGTCAGGGTCTCATTTTGTTGCTCAGGCTGG CTGGGAAAGAGCCCAAGAAATGATTTTTTTGTGGAGTCAGGGTCTCATTTTGTTGCTCAGGCTGG T C WDR33 Ensembl:ENSG00000136709 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs780854999 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13604976,Human_RBP_ID_23823872 18129 RMVar_ID_18129 Human_SNP_ID_91235893 A-to-I Human chr2 - 127802728 127802728 127802728 CGGTTCCTCCCTCCTCAGCCTCCCAAAATACTAGGATTACAAGGCATGAGCCACTGCACCCAGAC CGGTTCCTCCCTCCTCAGCCTCCCAAAATACTTGGATTACAAGGCATGAGCCACTGCACCCAGAC T A WDR33 Ensembl:ENSG00000136709 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1162007882 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13605315,Human_RBP_ID_17569887 18130 RMVar_ID_18130 Human_SNP_ID_91235894 A-to-I Human chr2 - 127802728 127802728 127802728 CGGTTCCTCCCTCCTCAGCCTCCCAAAATACTAGGATTACAAGGCATGAGCCACTGCACCCAGAC CGGTTCCTCCCTCCTCAGCCTCCCAAAATACTGGGATTACAAGGCATGAGCCACTGCACCCAGAC T C WDR33 Ensembl:ENSG00000136709 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1162007882 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13605315,Human_RBP_ID_17569887 18131 RMVar_ID_18131 Human_SNP_ID_91235897 A-to-I Human chr2 - 127802744 127802744 127802744 GAACTCCTGGGGTCATCGGTTCCTCCCTCCTCAGCCTCCCAAAATACTAGGATTACAAGGCATGA GAACTCCTGGGGTCATCGGTTCCTCCCTCCTCCGCCTCCCAAAATACTAGGATTACAAGGCATGA T G WDR33 Ensembl:ENSG00000136709 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1023411400 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6822186,Human_RBP_ID_13605320,Human_RBP_ID_17569887 18132 RMVar_ID_18132 Human_SNP_ID_91235918 A-to-I Human chr2 - 127802796 127802796 127802796 TTTGTGTTTTTTGGTATAGTCTGGGTTTTGCCATGTTGCCCAGTCTGGGCTCGAACTCCTGGGGT TTTGTGTTTTTTGGTATAGTCTGGGTTTTGCCGTGTTGCCCAGTCTGGGCTCGAACTCCTGGGGT T C WDR33 Ensembl:ENSG00000136709 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs771648091 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8500598,Human_RBP_ID_13605322,Human_RBP_ID_17569887 18133 RMVar_ID_18133 Human_SNP_ID_91236094 A-to-I Human chr2 - 127803562 127803562 127803562 ACATTGGTATTTTATTTTATTTATTTTTTGAGACAGTCTCCCTCTGTCACCTAGGCTGGAGTGCA ACATTGGTATTTTATTTTATTTATTTTTTGAGGCAGTCTCCCTCTGTCACCTAGGCTGGAGTGCA T C WDR33 Ensembl:ENSG00000136709 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1374817249 Functional Loss SNV dbSNP153 33..33 33 - - - 18134 RMVar_ID_18134 Human_SNP_ID_91246323 A-to-I Human chr2 - 127843846 127843846 127843846 GTTTCCGCCTCCCAAATGCTGAGATTAGAGGCATGAGTCACTGCACCCAGCCCGCAGCCTCTTTT GTTTCCGCCTCCCAAATGCTGAGATTAGAGGCTTGAGTCACTGCACCCAGCCCGCAGCCTCTTTT T A POLR2D Ensembl:ENSG00000144231 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs11539731 Functional Loss SNV dbSNP153 33..33 33 - - - 18135 RMVar_ID_18135 Human_SNP_ID_91246324 A-to-I Human chr2 - 127843846 127843846 127843846 GTTTCCGCCTCCCAAATGCTGAGATTAGAGGCATGAGTCACTGCACCCAGCCCGCAGCCTCTTTT GTTTCCGCCTCCCAAATGCTGAGATTAGAGGCGTGAGTCACTGCACCCAGCCCGCAGCCTCTTTT T C POLR2D Ensembl:ENSG00000144231 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs11539731 Functional Loss SNV dbSNP153 33..33 33 - - - 18136 RMVar_ID_18136 Human_SNP_ID_91246327 A-to-I Human chr2 - 127843852 127843852 127843852 CCACCTGTTTCCGCCTCCCAAATGCTGAGATTAGAGGCATGAGTCACTGCACCCAGCCCGCAGCC CCACCTGTTTCCGCCTCCCAAATGCTGAGATTGGAGGCATGAGTCACTGCACCCAGCCCGCAGCC T C POLR2D Ensembl:ENSG00000144231 Protein coding 3'UTR GSE100210;GSE112787 HepG2 cell line;293 Flip-In T-REx cells,empty vector - 29129909,29967493 RNA-Seq:(High) rs1558979107 Functional Loss SNV dbSNP153 33..33 33 - - - 18137 RMVar_ID_18137 Human_SNP_ID_91246329 A-to-I Human chr2 - 127843857 127843857 127843857 GCAGTCCACCTGTTTCCGCCTCCCAAATGCTGAGATTAGAGGCATGAGTCACTGCACCCAGCCCG GCAGTCCACCTGTTTCCGCCTCCCAAATGCTGGGATTAGAGGCATGAGTCACTGCACCCAGCCCG T C POLR2D Ensembl:ENSG00000144231 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs11539730 Functional Loss SNV dbSNP153 33..33 33 - - - 18138 RMVar_ID_18138 Human_SNP_ID_91246343 A-to-I Human chr2 - 127843887 127843887 127843887 CCCAGGCTGGTCTGGAATTTCTGACCTCTAGCAGTCCACCTGTTTCCGCCTCCCAAATGCTGAGA CCCAGGCTGGTCTGGAATTTCTGACCTCTAGCGGTCCACCTGTTTCCGCCTCCCAAATGCTGAGA T C POLR2D Ensembl:ENSG00000144231 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1363801769 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_533828,Human_RBP_ID_26476502 18139 RMVar_ID_18139 Human_SNP_ID_91246366 A-to-I Human chr2 - 127843951 127843947 127843951 CACAGGCACGAGCTACCATGCCTGGCTAATTTATTTTTTGTAGAGACGGGGTTTCGCCATGTTGC CACAGGCACGAGCTACCATGCCTGGCTAATTT____TTTGTAGAGACGGGGTTTCGCCATGTTGC AAAAT A POLR2D Ensembl:ENSG00000144231 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1234379363 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_18309725 18140 RMVar_ID_18140 Human_SNP_ID_91246367 A-to-I Human chr2 - 127843951 127843951 127843951 CACAGGCACGAGCTACCATGCCTGGCTAATTTATTTTTTGTAGAGACGGGGTTTCGCCATGTTGC CACAGGCACGAGCTACCATGCCTGGCTAATTTGTTTTTTGTAGAGACGGGGTTTCGCCATGTTGC T C POLR2D Ensembl:ENSG00000144231 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs779520910 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18309725 18141 RMVar_ID_18141 Human_SNP_ID_91246377 A-to-I Human chr2 - 127843980 127843980 127843980 CCCACCTCAGCCTCTTGGATAGCTGGGACCACAGGCACGAGCTACCATGCCTGGCTAATTTATTT CCCACCTCAGCCTCTTGGATAGCTGGGACCACGGGCACGAGCTACCATGCCTGGCTAATTTATTT T C POLR2D Ensembl:ENSG00000144231 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1280446547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6822338,Human_RBP_ID_13605690 18142 RMVar_ID_18142 Human_SNP_ID_91246606 A-to-I Human chr2 - 127844774 127844774 127844774 TGGCGGGCACCTGTAATCCTAGCTACTTGGGAAGCTGAGACAGGAGAATTGCTTGAACCCGGGAG TGGCGGGCACCTGTAATCCTAGCTACTTGGGAGGCTGAGACAGGAGAATTGCTTGAACCCGGGAG T C POLR2D Ensembl:ENSG00000144231 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1469391239 Functional Loss SNV dbSNP153 33..33 33 - - - 18143 RMVar_ID_18143 Human_SNP_ID_91246636 A-to-I Human chr2 - 127844847 127844847 127844847 AAGTTCGAGACCAGCCTGGCCAACGTTGTGAAACCCTGTCTCTACTAAAAATACAAAAATTGGCC AAGTTCGAGACCAGCCTGGCCAACGTTGTGAAGCCCTGTCTCTACTAAAAATACAAAAATTGGCC T C POLR2D Ensembl:ENSG00000144231 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs945489717 Functional Loss SNV dbSNP153 33..33 33 - - - 18144 RMVar_ID_18144 Human_SNP_ID_91246654 A-to-I Human chr2 - 127844891 127844891 127844891 CCAGCACTTTGGGAGGCCGAGGCGGGTGGATCACCAGAGGTCAGAAGTTCGAGACCAGCCTGGCC CCAGCACTTTGGGAGGCCGAGGCGGGTGGATCGCCAGAGGTCAGAAGTTCGAGACCAGCCTGGCC T C POLR2D Ensembl:ENSG00000144231 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1000884652 Functional Loss SNV dbSNP153 33..33 33 - - - 18145 RMVar_ID_18145 Human_SNP_ID_91246864 A-to-I Human chr2 - 127845472 127845472 127845472 ACTCTGGAGGCTGAGGCAGGAGAATTGCTTGAACCTGGGAGGCAGAGGGGGTGGCGAGCCAAGAT ACTCTGGAGGCTGAGGCAGGAGAATTGCTTGACCCTGGGAGGCAGAGGGGGTGGCGAGCCAAGAT T G POLR2D Ensembl:ENSG00000144231 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1472167126 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_533844 18146 RMVar_ID_18146 Human_SNP_ID_91246868 A-to-I Human chr2 - 127845504 127845504 127845504 GGGCGTGGTGGCGCATGCCTGTAATCTCAGCTACTCTGGAGGCTGAGGCAGGAGAATTGCTTGAA GGGCGTGGTGGCGCATGCCTGTAATCTCAGCTGCTCTGGAGGCTGAGGCAGGAGAATTGCTTGAA T C POLR2D Ensembl:ENSG00000144231 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1443360856 Functional Loss SNV dbSNP153 33..33 33 - - - 18147 RMVar_ID_18147 Human_SNP_ID_91246888 A-to-I Human chr2 - 127845557 127845553 127845558 CATCCTGACCAACATGGAGAAACCCCGTCTCTACTTAAAATACAAAATTAGCGGGGCGTGGTGGC CATCCTGACCAACATGGAGAAACCCCGTCTC_____AAAATACAAAATTAGCGGGGCGTGGTGGC TAAGTA T POLR2D Ensembl:ENSG00000144231 Protein coding 3'UTR GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 ASD brains,Fragile X samples from UC Davis FXTAS brain repository;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 30559470,31158229,31158229,31158229 RNA-Seq:(High) rs1410904961 Functional Loss DEL dbSNP153 32..36 33 - - - Human_RBP_ID_17939435 18148 RMVar_ID_18148 Human_SNP_ID_91246893 A-to-I Human chr2 - 127845576 127845576 127845576 GAGGTTGGGAGTTTGAGACCATCCTGACCAACATGGAGAAACCCCGTCTCTACTTAAAATACAAA GAGGTTGGGAGTTTGAGACCATCCTGACCAACGTGGAGAAACCCCGTCTCTACTTAAAATACAAA T C POLR2D Ensembl:ENSG00000144231 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1262958938 Functional Loss SNV dbSNP153 33..33 33 - - - 18149 RMVar_ID_18149 Human_SNP_ID_91247032 A-to-I Human chr2 - 127846080 127846078 127846080 CCTGGCTAATTTTTTGTGTTTTTAGTAGAGACAGGGTTTCACCACGTTCGCCAGGCTAGTCTTGA CCTGGCTAATTTTTTGTGTTTTTAGTAGAGAC__GGTTTCACCACGTTCGCCAGGCTAGTCTTGA CCT C POLR2D Ensembl:ENSG00000144231 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1558980015 Functional Loss DEL dbSNP153 33..34 33 - - - 18150 RMVar_ID_18150 Human_SNP_ID_91247064 A-to-I Human chr2 - 127846206 127846206 127846206 TCTGGCTGTGTTGCCCAGGATGCAATGGCGCAATCTTGGCTCACTGCAACCTCTGCCTTCTGGGT TCTGGCTGTGTTGCCCAGGATGCAATGGCGCATTCTTGGCTCACTGCAACCTCTGCCTTCTGGGT T A POLR2D Ensembl:ENSG00000144231 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs774983179 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27000398 18151 RMVar_ID_18151 Human_SNP_ID_91247065 A-to-I Human chr2 - 127846206 127846206 127846206 TCTGGCTGTGTTGCCCAGGATGCAATGGCGCAATCTTGGCTCACTGCAACCTCTGCCTTCTGGGT TCTGGCTGTGTTGCCCAGGATGCAATGGCGCAGTCTTGGCTCACTGCAACCTCTGCCTTCTGGGT T C POLR2D Ensembl:ENSG00000144231 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs774983179 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27000398 18152 RMVar_ID_18152 Human_SNP_ID_91247070 A-to-I Human chr2 - 127846214 127846214 127846214 AGATAGAGTCTGGCTGTGTTGCCCAGGATGCAATGGCGCAATCTTGGCTCACTGCAACCTCTGCC AGATAGAGTCTGGCTGTGTTGCCCAGGATGCAGTGGCGCAATCTTGGCTCACTGCAACCTCTGCC T C POLR2D Ensembl:ENSG00000144231 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs949851248 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27000398 18153 RMVar_ID_18153 Human_SNP_ID_91247079 A-to-I Human chr2 - 127846258 127846258 127846258 CAAGAATAAAAAATTCTTATTTTTATTTATTTATTTATTTTTTGAGATAGAGTCTGGCTGTGTTG CAAGAATAAAAAATTCTTATTTTTATTTATTTGTTTATTTTTTGAGATAGAGTCTGGCTGTGTTG T C POLR2D Ensembl:ENSG00000144231 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924373671 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6822370,Human_RBP_ID_13605738 18154 RMVar_ID_18154 Human_SNP_ID_91247083 A-to-I Human chr2 - 127846266 127846266 127846266 AAATAAGGCAAGAATAAAAAATTCTTATTTTTATTTATTTATTTATTTTTTGAGATAGAGTCTGG AAATAAGGCAAGAATAAAAAATTCTTATTTTTTTTTATTTATTTATTTTTTGAGATAGAGTCTGG T A POLR2D Ensembl:ENSG00000144231 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1299064411 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6822370,Human_RBP_ID_13605738,Human_RBP_ID_22243174 RMVar_hsa_circ_203111,RMVar_hsa_circ_83615 18155 RMVar_ID_18155 Human_SNP_ID_91247842 A-to-I Human chr2 - 127849209 127849209 127849209 GTGGAACTCCATCTCTACTAAAATACAAAATTAGCTGGGTGTGGTGGTGTGCGACTGTAGTCCCG GTGGAACTCCATCTCTACTAAAATACAAAATTTGCTGGGTGTGGTGGTGTGCGACTGTAGTCCCG T A POLR2D Ensembl:ENSG00000144231 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs766250579 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_203111,RMVar_hsa_circ_83615 18156 RMVar_ID_18156 Human_SNP_ID_91247843 A-to-I Human chr2 - 127849209 127849209 127849209 GTGGAACTCCATCTCTACTAAAATACAAAATTAGCTGGGTGTGGTGGTGTGCGACTGTAGTCCCG GTGGAACTCCATCTCTACTAAAATACAAAATTGGCTGGGTGTGGTGGTGTGCGACTGTAGTCCCG T C POLR2D Ensembl:ENSG00000144231 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs766250579 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_203111,RMVar_hsa_circ_83615 18157 RMVar_ID_18157 Human_SNP_ID_91248452 A-to-I Human chr2 - 127851485 127851485 127851485 GTGATCCTCCTGCCTTGGCCTCCCAAAGTGCTAGGATTACAGGCATGAGCTGCTAAGCCTGGCCT GTGATCCTCCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCTGCTAAGCCTGGCCT T C POLR2D Ensembl:ENSG00000144231 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1182993480 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_203112,RMVar_hsa_circ_317749 18158 RMVar_ID_18158 Human_SNP_ID_91252843 A-to-I Human chr2 - 127867512 127867512 127867512 GAACTCATGGGCTCAAGTGATCCTCCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG GAACTCATGGGCTCAAGTGATCCTCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG T C AMMECR1L Ensembl:ENSG00000144233 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs967864233 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_68644,RMVar_hsa_circ_105024,RMVar_hsa_circ_101272,RMVar_hsa_circ_203115,RMVar_hsa_circ_203114 18159 RMVar_ID_18159 Human_SNP_ID_91252859 A-to-I Human chr2 - 127867598 127867598 127867598 GGGACTACAGGCGCATCCCACACGCTCACTTAATTTTTGCGTTCTTAGTAGGGATGAGGTTTAAC GGGACTACAGGCGCATCCCACACGCTCACTTAGTTTTTGCGTTCTTAGTAGGGATGAGGTTTAAC T C AMMECR1L Ensembl:ENSG00000144233 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs536434058 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_68644,RMVar_hsa_circ_105024,RMVar_hsa_circ_101272,RMVar_hsa_circ_203115,RMVar_hsa_circ_203114 18160 RMVar_ID_18160 Human_SNP_ID_91252970 A-to-I Human chr2 - 127868047 127868047 127868047 TCTGGTGGCGAAACCTCGTCTCTACAAAAAATACAAATTCAGCTGGGTGTGGTGGCACACACCTG TCTGGTGGCGAAACCTCGTCTCTACAAAAAATTCAAATTCAGCTGGGTGTGGTGGCACACACCTG T A AMMECR1L Ensembl:ENSG00000144233 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs369050172 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_68644,RMVar_hsa_circ_105024,RMVar_hsa_circ_101272,RMVar_hsa_circ_203115,RMVar_hsa_circ_203114 18161 RMVar_ID_18161 Human_SNP_ID_91258507 A-to-I Human chr2 + 127889535 127889535 127889535 AGAAGGTTTTCTTTCTTTTTTTTTTTTTTCTGAGACAGGGTTTTGCTTTGTTGCCCAGGCTGGAG AGAAGGTTTTCTTTCTTTTTTTTTTTTTTCTGTGACAGGGTTTTGCTTTGTTGCCCAGGCTGGAG A T AC012306.4 Ensembl:ENSG00000286873 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1331953416 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2585162 18162 RMVar_ID_18162 Human_SNP_ID_91258543 A-to-I Human chr2 + 127889722 127889722 127889722 CAGCTAATTTTTGTAGAAAATGGAGTCTCCTTATGTTGCCCAGACTGGTCTCCAAACTCCTGGGC CAGCTAATTTTTGTAGAAAATGGAGTCTCCTTCTGTTGCCCAGACTGGTCTCCAAACTCCTGGGC A C AC012306.4 Ensembl:ENSG00000286873 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348071141 Functional Loss SNV dbSNP153 33..33 33 - - - 18163 RMVar_ID_18163 Human_SNP_ID_91260081 A-to-I Human chr2 + 127895293 127895293 127895293 TACCTCCCGGGCTCAAGTGATTGTCCTGCCTCAACCACCCAAGTAGCTGGGACTATAGTCGTACG TACCTCCCGGGCTCAAGTGATTGTCCTGCCTCGACCACCCAAGTAGCTGGGACTATAGTCGTACG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs918402234 Functional Loss SNV dbSNP153 33..33 33 - - - 18164 RMVar_ID_18164 Human_SNP_ID_91272382 A-to-I Human chr2 - 127944147 127944147 127944147 ACACCCCCTAGTCCCAGCTACCTGGGAAGCTGAGGTGGGAGGAACTCTTGAGCCCGGAAGACCAA ACACCCCCTAGTCCCAGCTACCTGGGAAGCTGTGGTGGGAGGAACTCTTGAGCCCGGAAGACCAA T A SAP130 Ensembl:ENSG00000136715 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs757270336 Functional Loss SNV dbSNP153 33..33 33 - - - 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_203126,RMVar_hsa_circ_203127 18165 RMVar_ID_18165 Human_SNP_ID_91284203 A-to-I Human chr2 - 127989227 127989227 127989227 AGGCGTGGTGGCGGGGGCCTGTAGTCCTAGCTACTCGGGAGGCTGAGGCGAGAGAATGGCGTGAA AGGCGTGGTGGCGGGGGCCTGTAGTCCTAGCTGCTCGGGAGGCTGAGGCGAGAGAATGGCGTGAA T C SAP130 Ensembl:ENSG00000136715 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1487856044 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85299,RMVar_hsa_circ_83471,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_14524,RMVar_hsa_circ_203131,RMVar_hsa_circ_17262,RMVar_hsa_circ_203132,RMVar_hsa_circ_313935,RMVar_hsa_circ_203133,RMVar_hsa_circ_33411,RMVar_hsa_circ_304162,RMVar_hsa_circ_363094,RMVar_hsa_circ_370542,RMVar_hsa_circ_355084,RMVar_hsa_circ_273096,RMVar_hsa_circ_203134,RMVar_hsa_circ_203135,RMVar_hsa_circ_203136 18166 RMVar_ID_18166 Human_SNP_ID_91284241 A-to-I Human chr2 - 127989369 127989369 127989369 TGTAAACGTTAGAAATAATATACCTCACTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGTGGA TGTAAACGTTAGAAATAATATACCTCACTGTAGTCCCAGCACTTTGGGAGGCTGAGGCGGGTGGA T C SAP130 Ensembl:ENSG00000136715 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1330745921 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85299,RMVar_hsa_circ_83471,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_14524,RMVar_hsa_circ_203131,RMVar_hsa_circ_17262,RMVar_hsa_circ_203132,RMVar_hsa_circ_313935,RMVar_hsa_circ_203133,RMVar_hsa_circ_33411,RMVar_hsa_circ_304162,RMVar_hsa_circ_363094,RMVar_hsa_circ_370542,RMVar_hsa_circ_355084,RMVar_hsa_circ_273096,RMVar_hsa_circ_203134,RMVar_hsa_circ_203135,RMVar_hsa_circ_203136 18167 RMVar_ID_18167 Human_SNP_ID_91288443 A-to-I Human chr2 - 128005563 128005563 128005563 TTGCTCAGGCTGGAGTTCAGTGGCGCGGTCTCAGCTCACTGCAGTCTCCACCCCCCGGGTTCAAG TTGCTCAGGCTGGAGTTCAGTGGCGCGGTCTCGGCTCACTGCAGTCTCCACCCCCCGGGTTCAAG T C SAP130 Ensembl:ENSG00000136715 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs374529906 Functional Loss SNV dbSNP153 33..33 33 - - - 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 18168 RMVar_ID_18168 Human_SNP_ID_91290072 A-to-I Human chr2 - 128011945 128011945 128011945 AGCTGGGCATGGTGGTGCGTGCCTGTAATCCCAGCTACCTGGGAGGCTGAGGTGGGAGAATCACT AGCTGGGCATGGTGGTGCGTGCCTGTAATCCCGGCTACCTGGGAGGCTGAGGTGGGAGAATCACT T C SAP130 Ensembl:ENSG00000136715 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1445247883 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83706,RMVar_hsa_circ_83471,RMVar_hsa_circ_203125,RMVar_hsa_circ_74347,RMVar_hsa_circ_75753,RMVar_hsa_circ_203132,RMVar_hsa_circ_119827,RMVar_hsa_circ_62664,RMVar_hsa_circ_203138,RMVar_hsa_circ_74292,RMVar_hsa_circ_203137,RMVar_hsa_circ_79784,RMVar_hsa_circ_203146,RMVar_hsa_circ_4033,RMVar_hsa_circ_203149,RMVar_hsa_circ_325962,RMVar_hsa_circ_328739,RMVar_hsa_circ_330709,RMVar_hsa_circ_203150 18169 RMVar_ID_18169 Human_SNP_ID_91290167 A-to-I Human chr2 - 128012348 128012348 128012348 CTCCTGCCTCAGCCTTCCAAGTACTTGGGACTACAGGTGTGCACCACCATGCCCGGCTAATTTTT CTCCTGCCTCAGCCTTCCAAGTACTTGGGACTGCAGGTGTGCACCACCATGCCCGGCTAATTTTT T C SAP130 Ensembl:ENSG00000136715 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs899842123 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83706,RMVar_hsa_circ_83471,RMVar_hsa_circ_203125,RMVar_hsa_circ_74347,RMVar_hsa_circ_75753,RMVar_hsa_circ_203132,RMVar_hsa_circ_119827,RMVar_hsa_circ_62664,RMVar_hsa_circ_203138,RMVar_hsa_circ_74292,RMVar_hsa_circ_203137,RMVar_hsa_circ_79784,RMVar_hsa_circ_203146,RMVar_hsa_circ_4033,RMVar_hsa_circ_203149,RMVar_hsa_circ_325962,RMVar_hsa_circ_328739,RMVar_hsa_circ_330709,RMVar_hsa_circ_203150 18170 RMVar_ID_18170 Human_SNP_ID_91293206 A-to-I Human chr2 - 128023523 128023523 128023523 TGCCCGCCTCAGCCTCCCAAAGTGCTGAGATTACAGGCATGAGCCACTGCGCCTGATGGTCTTTT TGCCCGCCTCAGCCTCCCAAAGTGCTGAGATTGCAGGCATGAGCCACTGCGCCTGATGGTCTTTT T C SAP130 Ensembl:ENSG00000136715 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1439417122 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_62664,RMVar_hsa_circ_203153 18171 RMVar_ID_18171 Human_SNP_ID_91318721 A-to-I Human chr2 + 128121545 128121545 128121545 CTCCTGCCTCAGCCTCCCAAGTAGCTGGTACTACAGACGTGCGTCACCATGCCCAGCTAAGTTTT CTCCTGCCTCAGCCTCCCAAGTAGCTGGTACTGCAGACGTGCGTCACCATGCCCAGCTAAGTTTT A G UGGT1 Ensembl:ENSG00000136731 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs944536434 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_203155,RMVar_hsa_circ_63867,RMVar_hsa_circ_303730,RMVar_hsa_circ_366591,RMVar_hsa_circ_326153,RMVar_hsa_circ_284247,RMVar_hsa_circ_289504,RMVar_hsa_circ_267270,RMVar_hsa_circ_81504,RMVar_hsa_circ_92381,RMVar_hsa_circ_70270,RMVar_hsa_circ_203159,RMVar_hsa_circ_203157,RMVar_hsa_circ_203158,RMVar_hsa_circ_203156,RMVar_hsa_circ_11323,RMVar_hsa_circ_50876,RMVar_hsa_circ_66363,RMVar_hsa_circ_20084,RMVar_hsa_circ_327955,RMVar_hsa_circ_359587,RMVar_hsa_circ_341358,RMVar_hsa_circ_336334,RMVar_hsa_circ_315119,RMVar_hsa_circ_266115,RMVar_hsa_circ_295255,RMVar_hsa_circ_299810,RMVar_hsa_circ_43040,RMVar_hsa_circ_39224,RMVar_hsa_circ_26296,RMVar_hsa_circ_203168,RMVar_hsa_circ_203172,RMVar_hsa_circ_203173,RMVar_hsa_circ_203170,RMVar_hsa_circ_203171,RMVar_hsa_circ_203169,RMVar_hsa_circ_356283,RMVar_hsa_circ_203179,RMVar_hsa_circ_372163,RMVar_hsa_circ_203167,RMVar_hsa_circ_364228,RMVar_hsa_circ_360075,RMVar_hsa_circ_339679,RMVar_hsa_circ_297644,RMVar_hsa_circ_55158,RMVar_hsa_circ_278057,RMVar_hsa_circ_37416,RMVar_hsa_circ_71089,RMVar_hsa_circ_203182,RMVar_hsa_circ_203183,RMVar_hsa_circ_357219,RMVar_hsa_circ_17283 18172 RMVar_ID_18172 Human_SNP_ID_91318956 A-to-I Human chr2 + 128122483 128122483 128122483 TTGAACCCGGGAGGTGAAGGTTACAGTGAGCCAAGATCATGCCATTGCACTCCAGCCTGAGCAAC TTGAACCCGGGAGGTGAAGGTTACAGTGAGCCGAGATCATGCCATTGCACTCCAGCCTGAGCAAC A G UGGT1 Ensembl:ENSG00000136731 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1267572017 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_203155,RMVar_hsa_circ_63867,RMVar_hsa_circ_303730,RMVar_hsa_circ_366591,RMVar_hsa_circ_326153,RMVar_hsa_circ_284247,RMVar_hsa_circ_289504,RMVar_hsa_circ_267270,RMVar_hsa_circ_81504,RMVar_hsa_circ_92381,RMVar_hsa_circ_70270,RMVar_hsa_circ_203159,RMVar_hsa_circ_203157,RMVar_hsa_circ_203158,RMVar_hsa_circ_203156,RMVar_hsa_circ_11323,RMVar_hsa_circ_50876,RMVar_hsa_circ_66363,RMVar_hsa_circ_20084,RMVar_hsa_circ_327955,RMVar_hsa_circ_359587,RMVar_hsa_circ_341358,RMVar_hsa_circ_336334,RMVar_hsa_circ_315119,RMVar_hsa_circ_266115,RMVar_hsa_circ_295255,RMVar_hsa_circ_299810,RMVar_hsa_circ_43040,RMVar_hsa_circ_39224,RMVar_hsa_circ_26296,RMVar_hsa_circ_203168,RMVar_hsa_circ_203172,RMVar_hsa_circ_203173,RMVar_hsa_circ_203170,RMVar_hsa_circ_203171,RMVar_hsa_circ_203169,RMVar_hsa_circ_356283,RMVar_hsa_circ_203179,RMVar_hsa_circ_372163,RMVar_hsa_circ_203167,RMVar_hsa_circ_364228,RMVar_hsa_circ_360075,RMVar_hsa_circ_339679,RMVar_hsa_circ_297644,RMVar_hsa_circ_55158,RMVar_hsa_circ_278057,RMVar_hsa_circ_37416,RMVar_hsa_circ_71089,RMVar_hsa_circ_203182,RMVar_hsa_circ_203183,RMVar_hsa_circ_357219,RMVar_hsa_circ_17283 18173 RMVar_ID_18173 Human_SNP_ID_91323604 A-to-I Human chr2 + 128140817 128140817 128140817 TCCTGCCTCAGCTTCCTGGAATAGCTGAGACTACAGGCATGCATCACCATACCCAGCTAATTTTG TCCTGCCTCAGCTTCCTGGAATAGCTGAGACTCCAGGCATGCATCACCATACCCAGCTAATTTTG A C UGGT1 Ensembl:ENSG00000136731 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1346620589 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3708,RMVar_hsa_circ_203155,RMVar_hsa_circ_303730,RMVar_hsa_circ_267270,RMVar_hsa_circ_81504,RMVar_hsa_circ_92381,RMVar_hsa_circ_203157,RMVar_hsa_circ_203156,RMVar_hsa_circ_11323,RMVar_hsa_circ_50876,RMVar_hsa_circ_66363,RMVar_hsa_circ_327955,RMVar_hsa_circ_266115,RMVar_hsa_circ_295255,RMVar_hsa_circ_299810,RMVar_hsa_circ_43040,RMVar_hsa_circ_39224,RMVar_hsa_circ_26296,RMVar_hsa_circ_203168,RMVar_hsa_circ_203170,RMVar_hsa_circ_203169,RMVar_hsa_circ_203179,RMVar_hsa_circ_372163,RMVar_hsa_circ_203167,RMVar_hsa_circ_55158,RMVar_hsa_circ_278057,RMVar_hsa_circ_37416,RMVar_hsa_circ_203183,RMVar_hsa_circ_349287,RMVar_hsa_circ_9636,RMVar_hsa_circ_363191,RMVar_hsa_circ_299654,RMVar_hsa_circ_93032,RMVar_hsa_circ_66823,RMVar_hsa_circ_203184,RMVar_hsa_circ_203186,RMVar_hsa_circ_203187,RMVar_hsa_circ_203185,RMVar_hsa_circ_48021,RMVar_hsa_circ_357465,RMVar_hsa_circ_203190,RMVar_hsa_circ_31493,RMVar_hsa_circ_203191,RMVar_hsa_circ_78060,RMVar_hsa_circ_293957,RMVar_hsa_circ_337758,RMVar_hsa_circ_82641,RMVar_hsa_circ_73359,RMVar_hsa_circ_203193,RMVar_hsa_circ_203194,RMVar_hsa_circ_203192 18174 RMVar_ID_18174 Human_SNP_ID_91335007 A-to-I Human chr2 + 128186602 128186602 128186602 GCACTCCAACCTGGGTGACAGAGTGGGACCCCATCTCTCAATAAATAAATAAATAAATATCGCCA GCACTCCAACCTGGGTGACAGAGTGGGACCCCGTCTCTCAATAAATAAATAAATAAATATCGCCA A G UGGT1 Ensembl:ENSG00000136731 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1366779692 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266115,RMVar_hsa_circ_7535,RMVar_hsa_circ_65690,RMVar_hsa_circ_83982,RMVar_hsa_circ_203205,RMVar_hsa_circ_203206,RMVar_hsa_circ_367112,RMVar_hsa_circ_71266,RMVar_hsa_circ_203222,RMVar_hsa_circ_283194 18175 RMVar_ID_18175 Human_SNP_ID_91336220 A-to-I Human chr2 + 128191603 128191603 128191603 TTGTTCGGCCAGGCGTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGACGG TTGTTCGGCCAGGCGTGGTGGCTCACACCTGTGATCCCAGCACTTTGGGAGGCTGAGGCGGACGG A G UGGT1 Ensembl:ENSG00000136731 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1485801338 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83982,RMVar_hsa_circ_203205 18176 RMVar_ID_18176 Human_SNP_ID_91336531 A-to-I Human chr2 + 128192917 128192917 128192917 GAAACAGTTTCCGGTCAGGCACAGTGGCTTACACCTGTAATCCCAGCACTTTGGGAAGCCGAGGC GAAACAGTTTCCGGTCAGGCACAGTGGCTTACCCCTGTAATCCCAGCACTTTGGGAAGCCGAGGC A C UGGT1 Ensembl:ENSG00000136731 Protein coding 3'UTR GSE47997;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831 K562 cells&HepG2 cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line - 23474544,29129909,29796672,31158229,32596459 RNA-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 18177 RMVar_ID_18177 Human_SNP_ID_91336532 A-to-I Human chr2 + 128192917 128192917 128192917 GAAACAGTTTCCGGTCAGGCACAGTGGCTTACACCTGTAATCCCAGCACTTTGGGAAGCCGAGGC GAAACAGTTTCCGGTCAGGCACAGTGGCTTACGCCTGTAATCCCAGCACTTTGGGAAGCCGAGGC A G UGGT1 Ensembl:ENSG00000136731 Protein coding 3'UTR GSE47997;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831 K562 cells&HepG2 cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line - 23474544,29129909,29796672,31158229,32596459 RNA-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 18178 RMVar_ID_18178 Human_SNP_ID_91336537 A-to-I Human chr2 + 128192929 128192929 128192929 GGTCAGGCACAGTGGCTTACACCTGTAATCCCAGCACTTTGGGAAGCCGAGGCGGGCGGATTATG GGTCAGGCACAGTGGCTTACACCTGTAATCCCTGCACTTTGGGAAGCCGAGGCGGGCGGATTATG A T UGGT1 Ensembl:ENSG00000136731 Protein coding 3'UTR GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs766904387 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1512304,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_2327216,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 18179 RMVar_ID_18179 Human_SNP_ID_91336572 A-to-I Human chr2 + 128193066 128193065 128193066 GGGCATGGTGGCACACACCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAA GGGCATGGTGGCACACACCTGTAGTCCCAGCT_CTCGGGAGGCTGAGGCAGGAGAATCACTTGAA TA T UGGT1 Ensembl:ENSG00000136731 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1260710374 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_83982,RMVar_hsa_circ_203205 18180 RMVar_ID_18180 Human_SNP_ID_91336656 A-to-I Human chr2 + 128193272 128193271 128193273 TGCTGTCCTTAAGCCCTCGTGGGTTTTTTTTTAAGAGAGTCTCATTCTGTCACCCAGGCTGGAGT TGCTGTCCTTAAGCCCTCGTGGGTTTTTTTTT__GAGAGTCTCATTCTGTCACCCAGGCTGGAGT TAA T UGGT1 Ensembl:ENSG00000136731 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs968327479 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_4580990,Human_RBP_ID_23310349 RMVar_hsa_circ_83982,RMVar_hsa_circ_203205 18181 RMVar_ID_18181 Human_SNP_ID_91336691 A-to-I Human chr2 + 128193426 128193426 128193426 GGCGCCTGCCACCATGCCTGGTTAATTTTTGTATTTTTAGTAGAGATGGGGTTTTACCATGTTGG GGCGCCTGCCACCATGCCTGGTTAATTTTTGTGTTTTTAGTAGAGATGGGGTTTTACCATGTTGG A G UGGT1 Ensembl:ENSG00000136731 Protein coding 3'UTR GSE47997;GSE38233;GSE99789 K562 cells&HepG2 cells;cultured B-cells;esophageal squamous carcinoma cells,EC109 - 23474544,24183664,29796672 RNA-Seq:(High) rs1404053660 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83982,RMVar_hsa_circ_203205 18182 RMVar_ID_18182 Human_SNP_ID_91336692 A-to-I Human chr2 + 128193435 128193435 128193435 CACCATGCCTGGTTAATTTTTGTATTTTTAGTAGAGATGGGGTTTTACCATGTTGGTTGGCCAGG CACCATGCCTGGTTAATTTTTGTATTTTTAGTGGAGATGGGGTTTTACCATGTTGGTTGGCCAGG A G UGGT1 Ensembl:ENSG00000136731 Protein coding 3'UTR GSE47997;GSE38233;GSE99789 K562 cells&HepG2 cells;cultured B-cells;esophageal squamous carcinoma cells,EC109 - 23474544,24183664,29796672 RNA-Seq:(High) rs1416638900 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83982,RMVar_hsa_circ_203205 18183 RMVar_ID_18183 Human_SNP_ID_91336711 A-to-I Human chr2 + 128193520 128193520 128193520 TCAGGTGGTGATCTGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTATGT TCAGGTGGTGATCTGCCCACCTCGGCCTCCCAGAGTGCTGGGATTACAGGCGTGAGCCACTATGT A G UGGT1 Ensembl:ENSG00000136731 Protein coding 3'UTR GSE47997;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831 K562 cells&HepG2 cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line - 23474544,29129909,29796672,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs1181725088 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569896,Human_RBP_ID_22722029 RMVar_hsa_circ_83982,RMVar_hsa_circ_203205 18184 RMVar_ID_18184 Human_SNP_ID_91336859 A-to-I Human chr2 + 128194115 128194114 128194116 ATTGTTGCGTGGTTTTTTTCCCCCCTCAAGACAGAGATTTGCTCTTGTTGCCCAGGGTGGAGTAC ATTGTTGCGTGGTTTTTTTCCCCCCTCAAGAC__AGATTTGCTCTTGTTGCCCAGGGTGGAGTAC CAG C UGGT1 Ensembl:ENSG00000136731 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1349834068 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_2585270,Human_RBP_ID_8203016,Human_RBP_ID_26486686 RMVar_hsa_circ_83982,RMVar_hsa_circ_203205 18185 RMVar_ID_18185 Human_SNP_ID_91336860 A-to-I Human chr2 + 128194115 128194115 128194115 ATTGTTGCGTGGTTTTTTTCCCCCCTCAAGACAGAGATTTGCTCTTGTTGCCCAGGGTGGAGTAC ATTGTTGCGTGGTTTTTTTCCCCCCTCAAGACTGAGATTTGCTCTTGTTGCCCAGGGTGGAGTAC A T UGGT1 Ensembl:ENSG00000136731 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1331936006 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2585270,Human_RBP_ID_8203016,Human_RBP_ID_26486686 RMVar_hsa_circ_83982,RMVar_hsa_circ_203205 18186 RMVar_ID_18186 Human_SNP_ID_91336875 A-to-I Human chr2 + 128194192 128194192 128194192 TTGGCTCACTGCAACCTCTGCCTCCTGGGTTCAGGTGATTCTCCTGCCTCAGCCTTCCGAGTAGC TTGGCTCACTGCAACCTCTGCCTCCTGGGTTCCGGTGATTCTCCTGCCTCAGCCTTCCGAGTAGC A C UGGT1 Ensembl:ENSG00000136731 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs1199473704 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83982,RMVar_hsa_circ_203205 18187 RMVar_ID_18187 Human_SNP_ID_91336904 A-to-I Human chr2 + 128194281 128194281 128194281 CACCCGGCTAATTTTTGCTTTTTTTTTTTTTGAGACAGAATCTCGCTCTGTTGCTCAGGCTGGAG CACCCGGCTAATTTTTGCTTTTTTTTTTTTTGTGACAGAATCTCGCTCTGTTGCTCAGGCTGGAG A T UGGT1 Ensembl:ENSG00000136731 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1451168304 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13608459,Human_RBP_ID_17570869 RMVar_hsa_circ_83982,RMVar_hsa_circ_203205 18188 RMVar_ID_18188 Human_SNP_ID_91336906 A-to-I Human chr2 + 128194285 128194285 128194285 CGGCTAATTTTTGCTTTTTTTTTTTTTGAGACAGAATCTCGCTCTGTTGCTCAGGCTGGAGTGGA CGGCTAATTTTTGCTTTTTTTTTTTTTGAGACGGAATCTCGCTCTGTTGCTCAGGCTGGAGTGGA A G UGGT1 Ensembl:ENSG00000136731 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1372458976 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13608459,Human_RBP_ID_17570869 RMVar_hsa_circ_83982,RMVar_hsa_circ_203205 18189 RMVar_ID_18189 Human_SNP_ID_91336916 A-to-I Human chr2 + 128194330 128194329 128194330 GTTGCTCAGGCTGGAGTGGAGTGCAGTGGCACAATCTCAGCTCACTGCAGCCTCTGCCTCCCGGG GTTGCTCAGGCTGGAGTGGAGTGCAGTGGCAC_ATCTCAGCTCACTGCAGCCTCTGCCTCCCGGG CA C UGGT1 Ensembl:ENSG00000136731 Protein coding 3'UTR GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,29796672,31158229,31158229,31158229 RNA-Seq:(High) rs1388068102 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_83982,RMVar_hsa_circ_203205 18190 RMVar_ID_18190 Human_SNP_ID_91336966 A-to-I Human chr2 + 128194528 128194528 128194528 ACCTCAAGTGATCCACCCGCATCGGCCCCCCAAAGTGCTGGGATTATAGGCGTGAACCACCGCGC ACCTCAAGTGATCCACCCGCATCGGCCCCCCAGAGTGCTGGGATTATAGGCGTGAACCACCGCGC A G UGGT1 Ensembl:ENSG00000136731 Protein coding 3'UTR GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,29796672,31158229,31158229,32596459 RNA-Seq:(High) rs1216547247 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83982,RMVar_hsa_circ_203205 18191 RMVar_ID_18191 Human_SNP_ID_91337099 A-to-I Human chr2 + 128195125 128195125 128195125 TCACGCCTGTAATCCTAGCACCTTGGGAGGCCAAGGCAGGCGGATCACCCGAGGTCAGGAGTTTG TCACGCCTGTAATCCTAGCACCTTGGGAGGCCGAGGCAGGCGGATCACCCGAGGTCAGGAGTTTG A G UGGT1 Ensembl:ENSG00000136731 Protein coding 3'UTR GSE38233;GSE100210;GSE100210;GSE107867;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;HepG2 cell line;ASD brains,temporal_cortex;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,29129909,30559470,32596459 RNA-Seq:(High) rs1193762688 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2216953 RMVar_hsa_circ_83982,RMVar_hsa_circ_203205 18192 RMVar_ID_18192 Human_SNP_ID_91337635 A-to-I Human chr2 + 128197464 128197464 128197464 AAAATTAGCCAGGCATGGTGGTATGTGCCTGTAGTCCCAGCTACTCAGAAGGCTGCGGTGGGAAG AAAATTAGCCAGGCATGGTGGTATGTGCCTGTGGTCCCAGCTACTCAGAAGGCTGCGGTGGGAAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs921511248 Functional Loss SNV dbSNP153 33..33 33 - - - 18193 RMVar_ID_18193 Human_SNP_ID_91338223 A-to-I Human chr2 + 128199638 128199638 128199638 ACAATCGCTTGAACCCGGCAGGCAGAGGTTGCAATGAGCCGAGATCATGCCATTGCACTGCGCCT ACAATCGCTTGAACCCGGCAGGCAGAGGTTGCCATGAGCCGAGATCATGCCATTGCACTGCGCCT A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1279151094 Functional Loss SNV dbSNP153 33..33 33 - - - 18194 RMVar_ID_18194 Human_SNP_ID_91338224 A-to-I Human chr2 + 128199638 128199638 128199638 ACAATCGCTTGAACCCGGCAGGCAGAGGTTGCAATGAGCCGAGATCATGCCATTGCACTGCGCCT ACAATCGCTTGAACCCGGCAGGCAGAGGTTGCGATGAGCCGAGATCATGCCATTGCACTGCGCCT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1279151094 Functional Loss SNV dbSNP153 33..33 33 - - - 18195 RMVar_ID_18195 Human_SNP_ID_91833908 A-to-I Human chr2 - 130158021 130158021 130158021 ATCCTCCCACCCTAGCCTCCTGAGTCATTAGGACTATAGGTGTGCACCACCACACCCAGCTAACT ATCCTCCCACCCTAGCCTCCTGAGTCATTAGGGCTATAGGTGTGCACCACCACACCCAGCTAACT T C SMPD4 Ensembl:ENSG00000136699 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1300922543 Functional Loss SNV dbSNP153 33..33 33 - - - 18196 RMVar_ID_18196 Human_SNP_ID_91834061 A-to-I Human chr2 - 130158473 130158473 130158473 CCATCTCTATGAAAAATAAAAATTAGCTGGGCATGGTGGCACACACTTGTCGTCCCAGCTACTCA CCATCTCTATGAAAAATAAAAATTAGCTGGGCGTGGTGGCACACACTTGTCGTCCCAGCTACTCA T C SMPD4 Ensembl:ENSG00000136699 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1045674416 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569901 18197 RMVar_ID_18197 Human_SNP_ID_91834236 A-to-I Human chr2 - 130159176 130159176 130159176 AGCCTGGGCAACATGGCGAAACCCCTGTCTCTACAAATACAAAAATTAGCCTGGTGTGGTGGTGT AGCCTGGGCAACATGGCGAAACCCCTGTCTCTCCAAATACAAAAATTAGCCTGGTGTGGTGGTGT T G SMPD4 Ensembl:ENSG00000136699 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs929472995 Functional Loss SNV dbSNP153 33..33 33 - - - 18198 RMVar_ID_18198 Human_SNP_ID_91834246 A-to-I Human chr2 - 130159222 130159222 130159222 GGGAGGTTGAGGCAGGCGGATTGCCTGAGCTCAGGAGTTTGAGACCAGCCTGGGCAACATGGCGA GGGAGGTTGAGGCAGGCGGATTGCCTGAGCTCGGGAGTTTGAGACCAGCCTGGGCAACATGGCGA T C SMPD4 Ensembl:ENSG00000136699 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1200153042 Functional Loss SNV dbSNP153 33..33 33 - - - 18199 RMVar_ID_18199 Human_SNP_ID_91834291 A-to-I Human chr2 - 130159394 130159394 130159394 CCTCAAGTGATCTGCCTGCCTTGGCCTCCCAAAGTGTTGGGATTATAGGCGTGAGCCACCGCACC CCTCAAGTGATCTGCCTGCCTTGGCCTCCCAACGTGTTGGGATTATAGGCGTGAGCCACCGCACC T G SMPD4 Ensembl:ENSG00000136699 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs376166494 Functional Loss SNV dbSNP153 33..33 33 - - - 18200 RMVar_ID_18200 Human_SNP_ID_91834333 A-to-I Human chr2 - 130159594 130159594 130159594 TCACTCCGTTGCCCAGGCTGGAATGCATTGACATGGTCTCGGCTCACTGCAATCTCCACCTCCCA TCACTCCGTTGCCCAGGCTGGAATGCATTGACGTGGTCTCGGCTCACTGCAATCTCCACCTCCCA T C SMPD4 Ensembl:ENSG00000136699 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1407299256 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_534070,Human_RBP_ID_22981637 Human_Splice_Rec_296754 18201 RMVar_ID_18201 Human_SNP_ID_91834334 A-to-I Human chr2 - 130159594 130159594 130159594 TCACTCCGTTGCCCAGGCTGGAATGCATTGACATGGTCTCGGCTCACTGCAATCTCCACCTCCCA TCACTCCGTTGCCCAGGCTGGAATGCATTGACCTGGTCTCGGCTCACTGCAATCTCCACCTCCCA T G SMPD4 Ensembl:ENSG00000136699 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1407299256 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_534070,Human_RBP_ID_22981637 Human_Splice_Rec_296754 18202 RMVar_ID_18202 Human_SNP_ID_91836059 A-to-I Human chr2 - 130166193 130166193 130166193 GTGATTCTCCCGCCTCAGCCCCCCGAGTAGCTAGGATTACAGGTGCCCACTGCCATGCTCAGCTA GTGATTCTCCCGCCTCAGCCCCCCGAGTAGCTGGGATTACAGGTGCCCACTGCCATGCTCAGCTA T C SMPD4 Ensembl:ENSG00000136699 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs745791240 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94324,RMVar_hsa_circ_203235,RMVar_hsa_circ_42299,RMVar_hsa_circ_56404,RMVar_hsa_circ_330421 18203 RMVar_ID_18203 Human_SNP_ID_91836379 A-to-I Human chr2 - 130167397 130167397 130167397 GTTCAGCCAGCTGGGCATGGTGGCTCGTGCCTATAATCCCCAGCACTTTGCGAGGCCTAGGTGGG GTTCAGCCAGCTGGGCATGGTGGCTCGTGCCTGTAATCCCCAGCACTTTGCGAGGCCTAGGTGGG T C SMPD4 Ensembl:ENSG00000136699 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1182234931 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3594958,Human_RBP_ID_22360080,Human_RBP_ID_25461404 RMVar_hsa_circ_94324,RMVar_hsa_circ_203235,RMVar_hsa_circ_42299,RMVar_hsa_circ_56404,RMVar_hsa_circ_330421 18204 RMVar_ID_18204 Human_SNP_ID_91836959 A-to-I Human chr2 - 130169684 130169684 130169684 AAGTATGGTGATGTGCAACTATGGTCCCAGCTACTCAGGAGGCTGAGGTGGGAGGATCACTTGTG AAGTATGGTGATGTGCAACTATGGTCCCAGCTGCTCAGGAGGCTGAGGTGGGAGGATCACTTGTG T C SMPD4 Ensembl:ENSG00000136699 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1231429727 Functional Loss SNV dbSNP153 33..33 33 - - - 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 18205 RMVar_ID_18205 Human_SNP_ID_91837241 A-to-I Human chr2 - 130170648 130170648 130170648 GTGATCCTCCCACTTCAACCTCCCAAGTAGCTAGTACTATAAGCATGCACCCCCACACCTAGCTT GTGATCCTCCCACTTCAACCTCCCAAGTAGCTGGTACTATAAGCATGCACCCCCACACCTAGCTT T C SMPD4 Ensembl:ENSG00000136699 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1466853947 Functional Loss SNV dbSNP153 33..33 33 - - - 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 18206 RMVar_ID_18206 Human_SNP_ID_91837305 A-to-I Human chr2 - 130170898 130170898 130170898 GGTCAGCATGCCCGACTAATTTTTGTATTTTTAGTAGTAACGGGGTTTCACCATGTTGGCCAGGC GGTCAGCATGCCCGACTAATTTTTGTATTTTTGGTAGTAACGGGGTTTCACCATGTTGGCCAGGC T C SMPD4 Ensembl:ENSG00000136699 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs572035392 Functional Loss SNV dbSNP153 33..33 33 - - - 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 18207 RMVar_ID_18207 Human_SNP_ID_91842319 A-to-I Human chr2 + 130187002 130187002 130187002 ACTTTGGGAGGCTGAGGCAGGATCATCACTTGAAGCTCGGAGTTTGAGACCAGCCTGGGCAAAAT ACTTTGGGAGGCTGAGGCAGGATCATCACTTGCAGCTCGGAGTTTGAGACCAGCCTGGGCAAAAT A C MZT2B Ensembl:ENSG00000152082 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1234053972 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108910,RMVar_hsa_circ_203239 18208 RMVar_ID_18208 Human_SNP_ID_91842437 A-to-I Human chr2 + 130187371 130187371 130187371 TACCACACGTGGCTAATTTTTTAATTTTTTGTAGAGATGGAGGTCTCACTGTGTTGTCCCAGCTG TACCACACGTGGCTAATTTTTTAATTTTTTGTGGAGATGGAGGTCTCACTGTGTTGTCCCAGCTG A G MZT2B Ensembl:ENSG00000152082 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1414333259 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18745920 RMVar_hsa_circ_108910,RMVar_hsa_circ_203239 18209 RMVar_ID_18209 Human_SNP_ID_91887392 A-to-I Human chr2 + 130362231 130362231 130362231 GCCTCAAGCTGTCCTTCCACCTCGGCCTCCCAAAGTGCTAAGATTACAGGCATGAGCCACTGCAT GCCTCAAGCTGTCCTTCCACCTCGGCCTCCCAGAGTGCTAAGATTACAGGCATGAGCCACTGCAT A G PTPN18 Ensembl:ENSG00000072135 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1485412470 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_297328 RMVar_hsa_circ_127523,RMVar_hsa_circ_203249 18210 RMVar_ID_18210 Human_SNP_ID_91960212 A-to-I Human chr2 + 130675143 130675143 130675143 CATCATGAAGACCGCAGATTAATAGACCCCGCAACAGCTTGTACCGTCAGTGGGTAAAAGCTACA CATCATGAAGACCGCAGATTAATAGACCCCGCGACAGCTTGTACCGTCAGTGGGTAAAAGCTACA A G lnc-POTEJ-1 RNACentral:URS00008C3E9C lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs927222006 Functional Loss SNV dbSNP153 33..33 33 - - - 18211 RMVar_ID_18211 Human_SNP_ID_92024487 A-to-I Human chr2 + 130922208 130922208 130922208 CCTGACCAACATGGAGAAACCCTGTCTCTACTAAAAACCACAAAAATTAGCCGGGCATGGTGGCG CCTGACCAACATGGAGAAACCCTGTCTCTACTGAAAACCACAAAAATTAGCCGGGCATGGTGGCG A G ARHGEF4 Ensembl:ENSG00000136002 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973620992 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_311556,RMVar_hsa_circ_96348,RMVar_hsa_circ_203253 18212 RMVar_ID_18212 Human_SNP_ID_92047690 A-to-I Human chr2 + 131017573 131017573 131017573 GCTGAGACCCCAGCTGGGACTACTGAAAAGCCAAGAAAAGTAGTGACTCCTACAAGAAATCTGTT GCTGAGACCCCAGCTGGGACTACTGAAAAGCCGAGAAAAGTAGTGACTCCTACAAGAAATCTGTT A G ARHGEF4 Ensembl:ENSG00000136002 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1271498012 Functional Loss SNV dbSNP153 33..33 33 - - - 18213 RMVar_ID_18213 Human_SNP_ID_92059605 A-to-I Human chr2 - 131061682 131061682 131061682 CACCTCCCAGGTTCAGCTGATTCTCCCACCTCAGCTTCCCGAGTGGCTGGGACTACAGTCGTGTG CACCTCCCAGGTTCAGCTGATTCTCCCACCTCCGCTTCCCGAGTGGCTGGGACTACAGTCGTGTG T G FAM168B Ensembl:ENSG00000152102 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1457143483 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81988,RMVar_hsa_circ_88391,RMVar_hsa_circ_203264,RMVar_hsa_circ_79489,RMVar_hsa_circ_203265,RMVar_hsa_circ_203263,RMVar_hsa_circ_203268,RMVar_hsa_circ_352585,RMVar_hsa_circ_315146,RMVar_hsa_circ_87954,RMVar_hsa_circ_203269,RMVar_hsa_circ_203270 18214 RMVar_ID_18214 Human_SNP_ID_92060134 A-to-I Human chr2 - 131063654 131063654 131063654 CTCCTGCCTTGGCCTCCTAAATCGCTGAGACTACAGGTACACCCCACCATGCCTTGCTAATTTTT CTCCTGCCTTGGCCTCCTAAATCGCTGAGACTGCAGGTACACCCCACCATGCCTTGCTAATTTTT T C FAM168B Ensembl:ENSG00000152102 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs945152691 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13609926 RMVar_hsa_circ_81988,RMVar_hsa_circ_88391,RMVar_hsa_circ_203264,RMVar_hsa_circ_79489,RMVar_hsa_circ_203265,RMVar_hsa_circ_203263,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 18215 RMVar_ID_18215 Human_SNP_ID_92060164 A-to-I Human chr2 - 131063773 131063773 131063773 TTTTAAAATTATTATTATTAGTTTTTAGAGACAGGGTCTTGCTCAGTCGCCCAGGCTGGAGTGTG TTTTAAAATTATTATTATTAGTTTTTAGAGACCGGGTCTTGCTCAGTCGCCCAGGCTGGAGTGTG T G FAM168B Ensembl:ENSG00000152102 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs972161989 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13609932 RMVar_hsa_circ_81988,RMVar_hsa_circ_88391,RMVar_hsa_circ_203264,RMVar_hsa_circ_79489,RMVar_hsa_circ_203265,RMVar_hsa_circ_203263,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 18216 RMVar_ID_18216 Human_SNP_ID_92060715 A-to-I Human chr2 - 131065677 131065677 131065677 TCAAGCGATTCTCCTGCCTCAGCCTCCTGAGAAGCTGGAATTACAGGCGCTCTCCACCACGCCGG TCAAGCGATTCTCCTGCCTCAGCCTCCTGAGAGGCTGGAATTACAGGCGCTCTCCACCACGCCGG T C FAM168B Ensembl:ENSG00000152102 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1478813807 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81988,RMVar_hsa_circ_88391,RMVar_hsa_circ_203264,RMVar_hsa_circ_79489,RMVar_hsa_circ_203265,RMVar_hsa_circ_203263,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 18217 RMVar_ID_18217 Human_SNP_ID_92061630 A-to-I Human chr2 - 131069010 131069010 131069010 ATGGGCCACCCATCTCATTATTATTTTGAGACAGGGTCTTGCTCTGTCGCCCAGGCTGCAGTGCA ATGGGCCACCCATCTCATTATTATTTTGAGACTGGGTCTTGCTCTGTCGCCCAGGCTGCAGTGCA T A FAM168B Ensembl:ENSG00000152102 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs963473395 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81988,RMVar_hsa_circ_88391,RMVar_hsa_circ_203264,RMVar_hsa_circ_79489,RMVar_hsa_circ_203265,RMVar_hsa_circ_203263,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 18218 RMVar_ID_18218 Human_SNP_ID_92061631 A-to-I Human chr2 - 131069010 131069010 131069010 ATGGGCCACCCATCTCATTATTATTTTGAGACAGGGTCTTGCTCTGTCGCCCAGGCTGCAGTGCA ATGGGCCACCCATCTCATTATTATTTTGAGACGGGGTCTTGCTCTGTCGCCCAGGCTGCAGTGCA T C FAM168B Ensembl:ENSG00000152102 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs963473395 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81988,RMVar_hsa_circ_88391,RMVar_hsa_circ_203264,RMVar_hsa_circ_79489,RMVar_hsa_circ_203265,RMVar_hsa_circ_203263,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 18219 RMVar_ID_18219 Human_SNP_ID_92062666 A-to-I Human chr2 - 131072580 131072580 131072580 GTGGTAGATGCCTGTAATCCCAGCTACTCGGAAGGCTGAGGCAGGAGAATCGCTTGAAACGGAGG GTGGTAGATGCCTGTAATCCCAGCTACTCGGACGGCTGAGGCAGGAGAATCGCTTGAAACGGAGG T G FAM168B Ensembl:ENSG00000152102 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1245901306 Functional Loss SNV dbSNP153 33..33 33 - - - 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_203272 18220 RMVar_ID_18220 Human_SNP_ID_92062670 A-to-I Human chr2 - 131072587 131072587 131072587 GGGCGTGGTGGTAGATGCCTGTAATCCCAGCTACTCGGAAGGCTGAGGCAGGAGAATCGCTTGAA GGGCGTGGTGGTAGATGCCTGTAATCCCAGCTGCTCGGAAGGCTGAGGCAGGAGAATCGCTTGAA T C FAM168B Ensembl:ENSG00000152102 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1265640631 Functional Loss SNV dbSNP153 33..33 33 - - - 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_203272 18221 RMVar_ID_18221 Human_SNP_ID_92063172 A-to-I Human chr2 - 131074406 131074406 131074406 AGAACGCTTTCTGGCCAGGTGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGA AGAACGCTTTCTGGCCAGGTGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGA T C FAM168B Ensembl:ENSG00000152102 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs979033382 Functional Loss SNV dbSNP153 33..33 33 - - - 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_203272 18222 RMVar_ID_18222 Human_SNP_ID_92063765 A-to-I Human chr2 - 131076491 131076491 131076491 CCGCCACTGCACCCGGCTAATTTTTTTTTTGTACTTTTATTAGAGATGGGGTTTCATCGTGGTCT CCGCCACTGCACCCGGCTAATTTTTTTTTTGTTCTTTTATTAGAGATGGGGTTTCATCGTGGTCT T A FAM168B Ensembl:ENSG00000152102 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924224462 Functional Loss SNV dbSNP153 33..33 33 - - - 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_203272 18223 RMVar_ID_18223 Human_SNP_ID_92063766 A-to-I Human chr2 - 131076491 131076491 131076491 CCGCCACTGCACCCGGCTAATTTTTTTTTTGTACTTTTATTAGAGATGGGGTTTCATCGTGGTCT CCGCCACTGCACCCGGCTAATTTTTTTTTTGTGCTTTTATTAGAGATGGGGTTTCATCGTGGTCT T C FAM168B Ensembl:ENSG00000152102 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924224462 Functional Loss SNV dbSNP153 33..33 33 - - - 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_203272 18224 RMVar_ID_18224 Human_SNP_ID_92064481 A-to-I Human chr2 - 131078864 131078864 131078864 CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGTGTGCGCTACCATGCCTGAATAATTTTT CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTGCAGGTGTGCGCTACCATGCCTGAATAATTTTT T C FAM168B Ensembl:ENSG00000152102 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs531958365 Functional Loss SNV dbSNP153 33..33 33 - - - 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_203272 18225 RMVar_ID_18225 Human_SNP_ID_92064507 A-to-I Human chr2 - 131078949 131078949 131078949 AGGGTCTTGCTCTGTCATTCAGGCCCCAGTGCAGTGGTGTAGTCACGGCTCACTGCAGCCTCAAA AGGGTCTTGCTCTGTCATTCAGGCCCCAGTGCGGTGGTGTAGTCACGGCTCACTGCAGCCTCAAA T C FAM168B Ensembl:ENSG00000152102 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1306356894 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13610442 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_203272 18226 RMVar_ID_18226 Human_SNP_ID_92067195 A-to-I Human chr2 - 131088080 131088080 131088080 CACCACGCCCAGCTAATTTTTGTATTTTTAGCAGAGACTGGGTTTCACCATGTTGCCCAGGCTGG CACCACGCCCAGCTAATTTTTGTATTTTTAGCGGAGACTGGGTTTCACCATGTTGCCCAGGCTGG T C FAM168B Ensembl:ENSG00000152102 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs540755592 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88391,RMVar_hsa_circ_203265,RMVar_hsa_circ_346190,RMVar_hsa_circ_303327 18227 RMVar_ID_18227 Human_SNP_ID_92067200 A-to-I Human chr2 - 131088098 131088098 131088098 GGGATTACAGGTGTGTGCCACCACGCCCAGCTAATTTTTGTATTTTTAGCAGAGACTGGGTTTCA GGGATTACAGGTGTGTGCCACCACGCCCAGCTGATTTTTGTATTTTTAGCAGAGACTGGGTTTCA T C FAM168B Ensembl:ENSG00000152102 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1053147112 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88391,RMVar_hsa_circ_203265,RMVar_hsa_circ_346190,RMVar_hsa_circ_303327 18228 RMVar_ID_18228 Human_SNP_ID_92067536 A-to-I Human chr2 - 131089091 131089091 131089091 GTGGTGGCACATGCCTGTAATCCCAGCTACTCAGGAGGCTGAGACAGGAGAATCGCTTGAACCTG GTGGTGGCACATGCCTGTAATCCCAGCTACTCGGGAGGCTGAGACAGGAGAATCGCTTGAACCTG T C FAM168B Ensembl:ENSG00000152102 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs563231320 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88391,RMVar_hsa_circ_203265,RMVar_hsa_circ_346190,RMVar_hsa_circ_303327 18229 RMVar_ID_18229 Human_SNP_ID_92067555 A-to-I Human chr2 - 131089170 131089170 131089170 CCTGAGGTCGGAAGTTCGAGACCAACCTGACCAACGTGGAGAAACCCCGTCTCTACTAAAAATAC CCTGAGGTCGGAAGTTCGAGACCAACCTGACCGACGTGGAGAAACCCCGTCTCTACTAAAAATAC T C FAM168B Ensembl:ENSG00000152102 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1212558379 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88391,RMVar_hsa_circ_203265,RMVar_hsa_circ_346190,RMVar_hsa_circ_303327 18230 RMVar_ID_18230 Human_SNP_ID_92067571 A-to-I Human chr2 - 131089230 131089230 131089230 CCGGTGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGACTGGCGGATCACCTGA CCGGTGCAGTGGCTCACGCCTGTAATCCCAGCCCTTTGGGAGGCCAAGACTGGCGGATCACCTGA T G FAM168B Ensembl:ENSG00000152102 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1002274762 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88391,RMVar_hsa_circ_203265,RMVar_hsa_circ_346190,RMVar_hsa_circ_303327 18231 RMVar_ID_18231 Human_SNP_ID_92067573 A-to-I Human chr2 - 131089238 131089238 131089238 AGCTCGGCCCGGTGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGACTGGCGGA AGCTCGGCCCGGTGCAGTGGCTCACGCCTGTAGTCCCAGCACTTTGGGAGGCCAAGACTGGCGGA T C FAM168B Ensembl:ENSG00000152102 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1192393307 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88391,RMVar_hsa_circ_203265,RMVar_hsa_circ_346190,RMVar_hsa_circ_303327 18232 RMVar_ID_18232 Human_SNP_ID_92067574 A-to-I Human chr2 - 131089239 131089239 131089239 AAGCTCGGCCCGGTGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGACTGGCGG AAGCTCGGCCCGGTGCAGTGGCTCACGCCTGTCATCCCAGCACTTTGGGAGGCCAAGACTGGCGG T G FAM168B Ensembl:ENSG00000152102 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs949954932 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88391,RMVar_hsa_circ_203265,RMVar_hsa_circ_346190,RMVar_hsa_circ_303327 18233 RMVar_ID_18233 Human_SNP_ID_92067581 A-to-I Human chr2 - 131089255 131089255 131089255 AAACTAAAAATGTGGTAAGCTCGGCCCGGTGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGG AAACTAAAAATGTGGTAAGCTCGGCCCGGTGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG T C FAM168B Ensembl:ENSG00000152102 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs564371290 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88391,RMVar_hsa_circ_203265,RMVar_hsa_circ_346190,RMVar_hsa_circ_303327 18234 RMVar_ID_18234 Human_SNP_ID_92068144 A-to-I Human chr2 - 131090716 131090716 131090716 TCAAACAAAAAATTTGTATATATTATACATATATATGTTCATTTTGTAGAGATGGGAGTCTCACT TCAAACAAAAAATTTGTATATATTATACATATGTATGTTCATTTTGTAGAGATGGGAGTCTCACT T C FAM168B Ensembl:ENSG00000152102 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs989601933 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13610911 RMVar_hsa_circ_88391,RMVar_hsa_circ_203265 18235 RMVar_ID_18235 Human_SNP_ID_92068278 A-to-I Human chr2 - 131091190 131091190 131091190 AGATTACAGGCACATGCCACCCTGCCCAGGTAATGTTTGTGTTTTTAGTAGAGATGGGGTCTCAT AGATTACAGGCACATGCCACCCTGCCCAGGTAGTGTTTGTGTTTTTAGTAGAGATGGGGTCTCAT T C FAM168B Ensembl:ENSG00000152102 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs747816454 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88391,RMVar_hsa_circ_203265 18236 RMVar_ID_18236 Human_SNP_ID_92068281 A-to-I Human chr2 - 131091195 131091195 131091195 AGCTGAGATTACAGGCACATGCCACCCTGCCCAGGTAATGTTTGTGTTTTTAGTAGAGATGGGGT AGCTGAGATTACAGGCACATGCCACCCTGCCCCGGTAATGTTTGTGTTTTTAGTAGAGATGGGGT T G FAM168B Ensembl:ENSG00000152102 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1441645495 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88391,RMVar_hsa_circ_203265 18237 RMVar_ID_18237 Human_SNP_ID_92068295 A-to-I Human chr2 - 131091227 131091227 131091227 TCAAGTGATTCTCCTGCCTCAGCCTCCGGAGTAGCTGAGATTACAGGCACATGCCACCCTGCCCA TCAAGTGATTCTCCTGCCTCAGCCTCCGGAGTGGCTGAGATTACAGGCACATGCCACCCTGCCCA T C FAM168B Ensembl:ENSG00000152102 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1424581147 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88391,RMVar_hsa_circ_203265 18238 RMVar_ID_18238 Human_SNP_ID_92079098 A-to-I Human chr2 + 131130216 131130216 131130216 CAGGCATGCGCCACCATGCCCGGCTAATGTTTATATTTTTTGTAGAGCTAGGATTTCACTATGTT CAGGCATGCGCCACCATGCCCGGCTAATGTTTTTATTTTTTGTAGAGCTAGGATTTCACTATGTT A T PLEKHB2 Ensembl:ENSG00000115762 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984698111 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13611220 RMVar_hsa_circ_13672,RMVar_hsa_circ_107100,RMVar_hsa_circ_376122,RMVar_hsa_circ_203274,RMVar_hsa_circ_203278,RMVar_hsa_circ_301443,RMVar_hsa_circ_203276,RMVar_hsa_circ_305609,RMVar_hsa_circ_33415,RMVar_hsa_circ_299819,RMVar_hsa_circ_203279,RMVar_hsa_circ_117831,RMVar_hsa_circ_332134,RMVar_hsa_circ_203277,RMVar_hsa_circ_314213,RMVar_hsa_circ_203280,RMVar_hsa_circ_203281 18239 RMVar_ID_18239 Human_SNP_ID_92082901 A-to-I Human chr2 + 131145415 131145415 131145415 CAGACTGGATTGCAGTGACAGGATCTCAACTCACTGCAGCCCCCGCCTCCCAGGTTCAAGCAATT CAGACTGGATTGCAGTGACAGGATCTCAACTCGCTGCAGCCCCCGCCTCCCAGGTTCAAGCAATT A G PLEKHB2 Ensembl:ENSG00000115762 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1302427231 Functional Loss SNV dbSNP153 33..33 33 - - - 18240 RMVar_ID_18240 Human_SNP_ID_92082936 A-to-I Human chr2 + 131145524 131145523 131145525 GCTAATTTTTTTTTGGTAATTTTTTAAGAGACAGGGTTTCACTGTGTTGGCCAGGCTGGTCTAAA GCTAATTTTTTTTTGGTAATTTTTTAAGAGAC__GGTTTCACTGTGTTGGCCAGGCTGGTCTAAA CAG C PLEKHB2 Ensembl:ENSG00000115762 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1358388429 Functional Loss DEL dbSNP153 33..34 33 - - - 18241 RMVar_ID_18241 Human_SNP_ID_92082938 A-to-I Human chr2 + 131145524 131145524 131145524 GCTAATTTTTTTTTGGTAATTTTTTAAGAGACAGGGTTTCACTGTGTTGGCCAGGCTGGTCTAAA GCTAATTTTTTTTTGGTAATTTTTTAAGAGACCGGGTTTCACTGTGTTGGCCAGGCTGGTCTAAA A C PLEKHB2 Ensembl:ENSG00000115762 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1039929603 Functional Loss SNV dbSNP153 33..33 33 - - - 18242 RMVar_ID_18242 Human_SNP_ID_92173301 A-to-I Human chr2 - 131476751 131476751 131476751 TTTGTATTTTTTTGTAGAGACTGGGTTTCGCCATGTTGGTCGGGCTGATCTTGAACTCCAGACAT TTTGTATTTTTTTGTAGAGACTGGGTTTCGCCGTGTTGGTCGGGCTGATCTTGAACTCCAGACAT T C MZT2A Ensembl:ENSG00000173272 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs979894669 Functional Loss SNV dbSNP153 33..33 33 - - - 18243 RMVar_ID_18243 Human_SNP_ID_92176597 A-to-I Human chr2 - 131487923 131487923 131487923 ATCTCTACAAAACATACAAAAATTAGCAGGGCATGGTGGCACACATCTGTAGTTCCAACTACTTG ATCTCTACAAAACATACAAAAATTAGCAGGGCGTGGTGGCACACATCTGTAGTTCCAACTACTTG T C MZT2A Ensembl:ENSG00000173272 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1451828752 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114413,RMVar_hsa_circ_203287 18244 RMVar_ID_18244 Human_SNP_ID_92178757 A-to-I Human chr2 + 131494253 131494253 131494253 AGTAGAAAATACAAAAATTAGCCGGGCGTGGTAGCGGGCGCGTGTAATCCCAGCCACTTGGGAGG AGTAGAAAATACAAAAATTAGCCGGGCGTGGTGGCGGGCGCGTGTAATCCCAGCCACTTGGGAGG A G SMPD4BP Ensembl:ENSG00000152117 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1318851013 Functional Loss SNV dbSNP153 33..33 33 - - - 18245 RMVar_ID_18245 Human_SNP_ID_92180890 A-to-I Human chr2 + 131502495 131502495 131502495 TATGTGGGCTGGGAGTGGTGGCTGACGCCTGTAATTCCAGCACTTTGGGAGGCCGAGGTGGAGGG TATGTGGGCTGGGAGTGGTGGCTGACGCCTGTCATTCCAGCACTTTGGGAGGCCGAGGTGGAGGG A C SMPD4BP Ensembl:ENSG00000152117 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1377960574 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3641656,Human_RBP_ID_9297631,Human_RBP_ID_13611817,Human_RBP_ID_25462053 RMVar_hsa_circ_8355,RMVar_hsa_circ_52405,RMVar_hsa_circ_343371,RMVar_hsa_circ_5470 18246 RMVar_ID_18246 Human_SNP_ID_92180910 A-to-I Human chr2 + 131502589 131502589 131502589 CCTGGCCAACATGGTGAAACCTCATCTCTACTAAAAATACAAAAGTTAGCTGGGCATGGTGGTGC CCTGGCCAACATGGTGAAACCTCATCTCTACTGAAAATACAAAAGTTAGCTGGGCATGGTGGTGC A G SMPD4BP Ensembl:ENSG00000152117 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1176561681 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8355,RMVar_hsa_circ_52405,RMVar_hsa_circ_343371,RMVar_hsa_circ_5470 18247 RMVar_ID_18247 Human_SNP_ID_92181199 A-to-I Human chr2 + 131503255 131503255 131503255 GTGATCCTCCCACTTCAACCTGCCAAGTAGCTAGTACTATAAGCATGCACCCCTACACCTAGCTT GTGATCCTCCCACTTCAACCTGCCAAGTAGCTGGTACTATAAGCATGCACCCCTACACCTAGCTT A G SMPD4BP Ensembl:ENSG00000152117 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1459177960 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8355,RMVar_hsa_circ_52405,RMVar_hsa_circ_343371,RMVar_hsa_circ_5470 18248 RMVar_ID_18248 Human_SNP_ID_92181528 A-to-I Human chr2 + 131504215 131504215 131504215 AAAAAAAAAGCCAGGTGTGATGATGTGCAACTATGGTCCCAGCTACTCAGGAGACTGAGGTGGGA AAAAAAAAAGCCAGGTGTGATGATGTGCAACTGTGGTCCCAGCTACTCAGGAGACTGAGGTGGGA A G SMPD4BP Ensembl:ENSG00000152117 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs560530776 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8355,RMVar_hsa_circ_52405,RMVar_hsa_circ_343371,RMVar_hsa_circ_5470 18249 RMVar_ID_18249 Human_SNP_ID_92182172 A-to-I Human chr2 + 131506655 131506655 131506655 ACGGTGGCAGGCGCCTGTAATTTCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACACA ACGGTGGCAGGCGCCTGTAATTTCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACACA A G SMPD4BP Ensembl:ENSG00000152117 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs899053699 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8355,RMVar_hsa_circ_28575,RMVar_hsa_circ_5470,RMVar_hsa_circ_35467 18250 RMVar_ID_18250 Human_SNP_ID_92182188 A-to-I Human chr2 + 131506716 131506716 131506716 CACAGGAGGTGGAGACAGCAGTAAGCTGAGATAGTGCCATTGCACTCCAGCGTGGGTGACAGAAC CACAGGAGGTGGAGACAGCAGTAAGCTGAGATCGTGCCATTGCACTCCAGCGTGGGTGACAGAAC A C SMPD4BP Ensembl:ENSG00000152117 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1460496106 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17393361 RMVar_hsa_circ_8355,RMVar_hsa_circ_28575,RMVar_hsa_circ_5470,RMVar_hsa_circ_35467 18251 RMVar_ID_18251 Human_SNP_ID_92182559 A-to-I Human chr2 + 131508100 131508100 131508100 GCCAGGCTGGTCTTGAACTCCCAGCCTCAGGTAATCCACCCACCTTGGCCTCCCAAAGTGCTGGG GCCAGGCTGGTCTTGAACTCCCAGCCTCAGGTGATCCACCCACCTTGGCCTCCCAAAGTGCTGGG A G SMPD4BP Ensembl:ENSG00000152117 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1184524568 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8355,RMVar_hsa_circ_28575,RMVar_hsa_circ_5470,RMVar_hsa_circ_35467 18252 RMVar_ID_18252 Human_SNP_ID_92184057 A-to-I Human chr2 + 131513514 131513514 131513514 CCACCCACCCGGCTAATTTTTGTATTTTTAGTAGAGACGTAGTTTCACCATGTTGGCCAGGCTGG CCACCCACCCGGCTAATTTTTGTATTTTTAGTCGAGACGTAGTTTCACCATGTTGGCCAGGCTGG A C SMPD4BP Ensembl:ENSG00000152117 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1295151237 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17394135 RMVar_hsa_circ_35467 18253 RMVar_ID_18253 Human_SNP_ID_92184128 A-to-I Human chr2 + 131513809 131513809 131513809 AGCCTGGGCAACATGGCGAGACCCCTGTCTCTACAAAGAAATACAAAAATTAGCCTGGTGTGGTG AGCCTGGGCAACATGGCGAGACCCCTGTCTCTGCAAAGAAATACAAAAATTAGCCTGGTGTGGTG A G SMPD4BP Ensembl:ENSG00000152117 Pseudogene intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs984631280 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18515834,Human_RBP_ID_23825046 RMVar_hsa_circ_35467 18254 RMVar_ID_18254 Human_SNP_ID_92184132 A-to-I Human chr2 + 131513822 131513822 131513822 TGGCGAGACCCCTGTCTCTACAAAGAAATACAAAAATTAGCCTGGTGTGGTGGTGTGTGTGCCTG TGGCGAGACCCCTGTCTCTACAAAGAAATACAGAAATTAGCCTGGTGTGGTGGTGTGTGTGCCTG A G SMPD4BP Ensembl:ENSG00000152117 Pseudogene intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs546561635 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18515834 RMVar_hsa_circ_35467 18255 RMVar_ID_18255 Human_SNP_ID_92184155 A-to-I Human chr2 + 131513918 131513918 131513918 AGGATCCCTTAAGCCCTGGAGGCAGAGGCTGCAGTGAGCCCAGACCACGACACTACACTCCAGCG AGGATCCCTTAAGCCCTGGAGGCAGAGGCTGCGGTGAGCCCAGACCACGACACTACACTCCAGCG A G SMPD4BP Ensembl:ENSG00000152117 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs144208474 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18926895 RMVar_hsa_circ_35467 18256 RMVar_ID_18256 Human_SNP_ID_92184160 A-to-I Human chr2 + 131513927 131513927 131513927 TAAGCCCTGGAGGCAGAGGCTGCAGTGAGCCCAGACCACGACACTACACTCCAGCGTGGGTGACA TAAGCCCTGGAGGCAGAGGCTGCAGTGAGCCCTGACCACGACACTACACTCCAGCGTGGGTGACA A T SMPD4BP Ensembl:ENSG00000152117 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355554011 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18926895 RMVar_hsa_circ_35467 18257 RMVar_ID_18257 Human_SNP_ID_92184313 A-to-I Human chr2 + 131514508 131514508 131514508 CACGTGGTCAAACCCCATCTCTATGAAAAATAAAAATTAGCTGGGCGTGGTGGCACACACTTGTC CACGTGGTCAAACCCCATCTCTATGAAAAATAGAAATTAGCTGGGCGTGGTGGCACACACTTGTC A G SMPD4BP Ensembl:ENSG00000152117 Pseudogene intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1402198196 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35467 18258 RMVar_ID_18258 Human_SNP_ID_92184314 A-to-I Human chr2 + 131514509 131514509 131514509 ACGTGGTCAAACCCCATCTCTATGAAAAATAAAAATTAGCTGGGCGTGGTGGCACACACTTGTCG ACGTGGTCAAACCCCATCTCTATGAAAAATAAGAATTAGCTGGGCGTGGTGGCACACACTTGTCG A G SMPD4BP Ensembl:ENSG00000152117 Pseudogene intron GSE47997;GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1298977485 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35467 18259 RMVar_ID_18259 Human_SNP_ID_92184418 A-to-I Human chr2 + 131514879 131514879 131514879 TCTTATTTTTGAACCAGGTCTTAACTCTCACCAAGGCTGGAGTGCAGTGGCACGATCCTAGCTCA TCTTATTTTTGAACCAGGTCTTAACTCTCACCCAGGCTGGAGTGCAGTGGCACGATCCTAGCTCA A C SMPD4BP Ensembl:ENSG00000152117 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1351871067 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3595184,Human_RBP_ID_5198685,Human_RBP_ID_17394138,Human_RBP_ID_17569913 RMVar_hsa_circ_35467 18260 RMVar_ID_18260 Human_SNP_ID_92369476 A-to-I Human chr2 - 132195666 132195666 132195666 CTGCCTCAGCTTCTTGAGTAGCTGGGATTACAAGCACCCACCACCGTGCCCTGCTAATTTTTGAA CTGCCTCAGCTTCTTGAGTAGCTGGGATTACATGCACCCACCACCGTGCCCTGCTAATTTTTGAA T A ANKRD30BL Ensembl:ENSG00000163046 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1157115307 Functional Loss SNV dbSNP153 33..33 33 - - - 18261 RMVar_ID_18261 Human_SNP_ID_92398109 A-to-I Human chr2 - 132254421 132254421 132254421 AGCCCACTGCCCTGGCGGAACGCTGAGAAGACAGTCGAACTTGACTATCTAGAGGAAGTAAAAGT AGCCCACTGCCCTGGCGGAACGCTGAGAAGACTGTCGAACTTGACTATCTAGAGGAAGTAAAAGT T A ANKRD30BL Ensembl:ENSG00000163046 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs62164987 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_270137,Human_RBP_ID_280330,Human_RBP_ID_1020184,Human_RBP_ID_1098012,Human_RBP_ID_1193007,Human_RBP_ID_1592644,Human_RBP_ID_1897799,Human_RBP_ID_2585922,Human_RBP_ID_3595218,Human_RBP_ID_4581798,Human_RBP_ID_5199790,Human_RBP_ID_5275623,Human_RBP_ID_5423390,Human_RBP_ID_5445279,Human_RBP_ID_5469905,Human_RBP_ID_5502816,Human_RBP_ID_5588520,Human_RBP_ID_6824236,Human_RBP_ID_8111307,Human_RBP_ID_8260199,Human_RBP_ID_8500976,Human_RBP_ID_8842308,Human_RBP_ID_9093702,Human_RBP_ID_13612566,Human_RBP_ID_17017794,Human_RBP_ID_17063459,Human_RBP_ID_17068822,Human_RBP_ID_17273572,Human_RBP_ID_17388826,Human_RBP_ID_17503549,Human_RBP_ID_17697257,Human_RBP_ID_17939861,Human_RBP_ID_18180752,Human_RBP_ID_18200759,Human_RBP_ID_18209113,Human_RBP_ID_18309937,Human_RBP_ID_18442481,Human_RBP_ID_18515370,Human_RBP_ID_18533277,Human_RBP_ID_18746085,Human_RBP_ID_20436293,Human_RBP_ID_21930770,Human_RBP_ID_22394524,Human_RBP_ID_22422818,Human_RBP_ID_22504452,Human_RBP_ID_22816614,Human_RBP_ID_22981688,Human_RBP_ID_23133342,Human_RBP_ID_23181752,Human_RBP_ID_23280017,Human_RBP_ID_23311013,Human_RBP_ID_23825101,Human_RBP_ID_24486067,Human_RBP_ID_24533267,Human_RBP_ID_24538955,Human_RBP_ID_24540221,Human_RBP_ID_26476947,Human_RBP_ID_26657147,Human_RBP_ID_26749713,Human_RBP_ID_27000761,Human_RBP_ID_27158750,Human_RBP_ID_27294047,Human_RBP_ID_27474941,Human_RBP_ID_27563149,Human_RBP_ID_27686735 18262 RMVar_ID_18262 Human_SNP_ID_92398110 A-to-I Human chr2 - 132254421 132254421 132254421 AGCCCACTGCCCTGGCGGAACGCTGAGAAGACAGTCGAACTTGACTATCTAGAGGAAGTAAAAGT AGCCCACTGCCCTGGCGGAACGCTGAGAAGACGGTCGAACTTGACTATCTAGAGGAAGTAAAAGT T C ANKRD30BL Ensembl:ENSG00000163046 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs62164987 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_270137,Human_RBP_ID_280330,Human_RBP_ID_1020184,Human_RBP_ID_1098012,Human_RBP_ID_1193007,Human_RBP_ID_1592644,Human_RBP_ID_1897799,Human_RBP_ID_2585922,Human_RBP_ID_3595218,Human_RBP_ID_4581798,Human_RBP_ID_5199790,Human_RBP_ID_5275623,Human_RBP_ID_5423390,Human_RBP_ID_5445279,Human_RBP_ID_5469905,Human_RBP_ID_5502816,Human_RBP_ID_5588520,Human_RBP_ID_6824236,Human_RBP_ID_8111307,Human_RBP_ID_8260199,Human_RBP_ID_8500976,Human_RBP_ID_8842308,Human_RBP_ID_9093702,Human_RBP_ID_13612566,Human_RBP_ID_17017794,Human_RBP_ID_17063459,Human_RBP_ID_17068822,Human_RBP_ID_17273572,Human_RBP_ID_17388826,Human_RBP_ID_17503549,Human_RBP_ID_17697257,Human_RBP_ID_17939861,Human_RBP_ID_18180752,Human_RBP_ID_18200759,Human_RBP_ID_18209113,Human_RBP_ID_18309937,Human_RBP_ID_18442481,Human_RBP_ID_18515370,Human_RBP_ID_18533277,Human_RBP_ID_18746085,Human_RBP_ID_20436293,Human_RBP_ID_21930770,Human_RBP_ID_22394524,Human_RBP_ID_22422818,Human_RBP_ID_22504452,Human_RBP_ID_22816614,Human_RBP_ID_22981688,Human_RBP_ID_23133342,Human_RBP_ID_23181752,Human_RBP_ID_23280017,Human_RBP_ID_23311013,Human_RBP_ID_23825101,Human_RBP_ID_24486067,Human_RBP_ID_24533267,Human_RBP_ID_24538955,Human_RBP_ID_24540221,Human_RBP_ID_26476947,Human_RBP_ID_26657147,Human_RBP_ID_26749713,Human_RBP_ID_27000761,Human_RBP_ID_27158750,Human_RBP_ID_27294047,Human_RBP_ID_27474941,Human_RBP_ID_27563149,Human_RBP_ID_27686735 18263 RMVar_ID_18263 Human_SNP_ID_92398118 A-to-I Human chr2 - 132254434 132254434 132254434 AGCCCGCTGGGTCAGCCCACTGCCCTGGCGGAACGCTGAGAAGACAGTCGAACTTGACTATCTAG AGCCCGCTGGGTCAGCCCACTGCCCTGGCGGAGCGCTGAGAAGACAGTCGAACTTGACTATCTAG T C ANKRD30BL Ensembl:ENSG00000163046 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs62164988 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_270137,Human_RBP_ID_1098013,Human_RBP_ID_4627225,Human_RBP_ID_5199792,Human_RBP_ID_5275481,Human_RBP_ID_5469906,Human_RBP_ID_5588524,Human_RBP_ID_6968248,Human_RBP_ID_9093703,Human_RBP_ID_17068823,Human_RBP_ID_17697257,Human_RBP_ID_18180753,Human_RBP_ID_18200759,Human_RBP_ID_18209113,Human_RBP_ID_20436294,Human_RBP_ID_22391872,Human_RBP_ID_22981690,Human_RBP_ID_23280018,Human_RBP_ID_23311015,Human_RBP_ID_23825103,Human_RBP_ID_26487903,Human_RBP_ID_26749713 18264 RMVar_ID_18264 Human_SNP_ID_92412023 A-to-I Human chr2 - 132279169 132279169 132279169 TTCCTATCATTGTGAAGTAGAATTCACCAAGCATTGGATTGTTCACCCACTAATAGGGCATGTGA TTCCTATCATTGTGAAGTAGAATTCACCAAGCGTTGGATTGTTCACCCACTAATAGGGCATGTGA T C RF02543-029 RNACentral:URS000096B970 rRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs74856357 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_270166,Human_RBP_ID_1020210,Human_RBP_ID_1297311,Human_RBP_ID_5422363,Human_RBP_ID_5443967,Human_RBP_ID_5469973,Human_RBP_ID_5500930,Human_RBP_ID_6824366,Human_RBP_ID_8257296,Human_RBP_ID_8501034,Human_RBP_ID_9093758,Human_RBP_ID_17503610 18265 RMVar_ID_18265 Human_SNP_ID_92429885 A-to-I Human chr2 + 132347759 132347759 132347759 GCGCCGGGGGTCCGGGATCCTACATCGCAGGGACTGGGGATCTCCTGGGTTCTGTACTCCCCCAG GCGCCGGGGGTCCGGGATCCTACATCGCAGGGTCTGGGGATCTCCTGGGTTCTGTACTCCCCCAG A T AC097532.3 Ensembl:ENSG00000286833 lincRNA intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs768455657 Functional Loss SNV dbSNP153 33..33 33 - - - 18266 RMVar_ID_18266 Human_SNP_ID_93042204 A-to-I Human chr2 + 134924650 134924650 134924650 TTTTGTATTTTTAGTAGAGACGGGTTTTCACCATGTTGGTCTGGCTGGTCTCAAACTCCTGACCT TTTTGTATTTTTAGTAGAGACGGGTTTTCACCGTGTTGGTCTGGCTGGTCTCAAACTCCTGACCT A G CCNT2 Ensembl:ENSG00000082258 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956931850 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80857,RMVar_hsa_circ_203352 18267 RMVar_ID_18267 Human_SNP_ID_93048003 A-to-I Human chr2 + 134948234 134948234 134948234 TCAGCTACTTGGGAGGCTGAGGCGGGATGATCACTTGAGCACGGGAAGTCAGGGCTGCGGTAAGC TCAGCTACTTGGGAGGCTGAGGCGGGATGATCGCTTGAGCACGGGAAGTCAGGGCTGCGGTAAGC A G CCNT2 Ensembl:ENSG00000082258 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs951398538 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13614790 RMVar_hsa_circ_224,RMVar_hsa_circ_359432,RMVar_hsa_circ_203357,RMVar_hsa_circ_83299,RMVar_hsa_circ_203363,RMVar_hsa_circ_57271 18268 RMVar_ID_18268 Human_SNP_ID_93048482 A-to-I Human chr2 + 134949895 134949895 134949895 TCGGCTCGCTGCACCCTCCGCCTCCCGGGTTCAAGCAGTTCTCTGCCTCAGCCTCCTGAGTAGCT TCGGCTCGCTGCACCCTCCGCCTCCCGGGTTCGAGCAGTTCTCTGCCTCAGCCTCCTGAGTAGCT A G CCNT2 Ensembl:ENSG00000082258 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs571466188 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13614861 RMVar_hsa_circ_224,RMVar_hsa_circ_359432,RMVar_hsa_circ_203357,RMVar_hsa_circ_83299,RMVar_hsa_circ_203363,RMVar_hsa_circ_57271 18269 RMVar_ID_18269 Human_SNP_ID_93048613 A-to-I Human chr2 + 134950460 134950460 134950460 CAGGAGTTTGAGCCCAGCCTGAGCAACATGGCAAAACCACGTTTCTACTAAAAATACACACAAAC CAGGAGTTTGAGCCCAGCCTGAGCAACATGGCTAAACCACGTTTCTACTAAAAATACACACAAAC A T CCNT2 Ensembl:ENSG00000082258 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1221883076 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_224,RMVar_hsa_circ_359432,RMVar_hsa_circ_203357,RMVar_hsa_circ_83299,RMVar_hsa_circ_203363,RMVar_hsa_circ_57271 18270 RMVar_ID_18270 Human_SNP_ID_174691675 A-to-I Human chr4 - 15560020 15560020 15560020 CGAGACTAGCCTGGGGCACGTGGCAAAACCCCATCTCTACAAAAAATATAAAAATTAGCCAGGCA CGAGACTAGCCTGGGGCACGTGGCAAAACCCCTTCTCTACAAAAAATATAAAAATTAGCCAGGCA T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1363997073 Functional Loss SNV dbSNP153 33..33 33 - - - 18271 RMVar_ID_18271 Human_SNP_ID_174706429 A-to-I Human chr4 - 15622112 15622112 15622112 AAAGAGCATTGAGGCTGGGTGTGATGGCTTACACCTGTAATCCCAGCACTTTGGGAGGCCAACGC AAAGAGCATTGAGGCTGGGTGTGATGGCTTACGCCTGTAATCCCAGCACTTTGGGAGGCCAACGC T C FBXL5 Ensembl:ENSG00000118564 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs28540215 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_224897,RMVar_hsa_circ_39572,RMVar_hsa_circ_290403,RMVar_hsa_circ_291119,RMVar_hsa_circ_29747,RMVar_hsa_circ_224898 18272 RMVar_ID_18272 Human_SNP_ID_174711319 A-to-I Human chr4 - 15640318 15640318 15640318 AGTCTTGGCTGGGCATGGTGGTTCACGTCTATAATCCCAGCACTTGGGAAGCTGAGGCAGGACAG AGTCTTGGCTGGGCATGGTGGTTCACGTCTATCATCCCAGCACTTGGGAAGCTGAGGCAGGACAG T G FBXL5 Ensembl:ENSG00000118564 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1363161888 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_224897,RMVar_hsa_circ_290403,RMVar_hsa_circ_291119,RMVar_hsa_circ_224898,RMVar_hsa_circ_359283,RMVar_hsa_circ_287081,RMVar_hsa_circ_276030,RMVar_hsa_circ_224903,RMVar_hsa_circ_224904,RMVar_hsa_circ_224906,RMVar_hsa_circ_53951,RMVar_hsa_circ_273874,RMVar_hsa_circ_224905,RMVar_hsa_circ_319021,RMVar_hsa_circ_368066,RMVar_hsa_circ_274298,RMVar_hsa_circ_224908,RMVar_hsa_circ_224909,RMVar_hsa_circ_23300,RMVar_hsa_circ_356280 18273 RMVar_ID_18273 Human_SNP_ID_174711862 A-to-I Human chr4 - 15641981 15641981 15641981 CTCTGTCACCCATGCTGAGGTGCAGTGGTGCAATCTCGGCTCACCGCAACCTCCTTCTTCCAGGT CTCTGTCACCCATGCTGAGGTGCAGTGGTGCATTCTCGGCTCACCGCAACCTCCTTCTTCCAGGT T A FBXL5 Ensembl:ENSG00000118564 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs972326829 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_224897,RMVar_hsa_circ_290403,RMVar_hsa_circ_291119,RMVar_hsa_circ_224898,RMVar_hsa_circ_287081,RMVar_hsa_circ_276030,RMVar_hsa_circ_224903,RMVar_hsa_circ_224904,RMVar_hsa_circ_224906,RMVar_hsa_circ_273874,RMVar_hsa_circ_224905,RMVar_hsa_circ_319021,RMVar_hsa_circ_274298,RMVar_hsa_circ_224908,RMVar_hsa_circ_224909,RMVar_hsa_circ_333129,RMVar_hsa_circ_356280,RMVar_hsa_circ_224910 18274 RMVar_ID_18274 Human_SNP_ID_174714200 A-to-I Human chr4 - 15650749 15650749 15650749 GGGGTCCTGTAATCCCAGCTACTCAGGAGGCTAAGGCAGAATTGCTGGAATTGGCGATTGCACTC GGGGTCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGAATTGCTGGAATTGGCGATTGCACTC T C FBXL5 Ensembl:ENSG00000118564 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs373067118 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25788596 18275 RMVar_ID_18275 Human_SNP_ID_174718270 A-to-I Human chr4 - 15666704 15666704 15666704 CCTCAGCCTCCCGAGTAGATGGAATCACAGGCACACACCACCACACCTGGCTAATTTTTTTGATG CCTCAGCCTCCCGAGTAGATGGAATCACAGGCGCACACCACCACACCTGGCTAATTTTTTTGATG T C FBXL5 Ensembl:ENSG00000118564 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1003402645 Functional Loss SNV dbSNP153 33..33 33 - - - 18276 RMVar_ID_18276 Human_SNP_ID_174719286 A-to-I Human chr4 - 15671151 15671151 15671151 GGAAGGCTGAAGCTGGCAAATCACTTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGAGA GGAAGGCTGAAGCTGGCAAATCACTTGAGGTCGGGAGTTCGAGACCAGCCTGGCCAACATGGAGA T C FBXL5 Ensembl:ENSG00000118564 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1473356156 Functional Loss SNV dbSNP153 33..33 33 - - - 18277 RMVar_ID_18277 Human_SNP_ID_174719706 A-to-I Human chr4 - 15673223 15673223 15673223 GTTGTCCAGGCTGGTTTCAAACTTGTGGGCTCAAGCGATCCAGCTACCTCGGCCTCCCAAAGTGC GTTGTCCAGGCTGGTTTCAAACTTGTGGGCTCGAGCGATCCAGCTACCTCGGCCTCCCAAAGTGC T C FBXL5 Ensembl:ENSG00000118564 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1457040777 Functional Loss SNV dbSNP153 33..33 33 - - - 18278 RMVar_ID_18278 Human_SNP_ID_174719716 A-to-I Human chr4 - 15673248 15673248 15673248 TTTTGTAGAGACAGGATTTTGCCATGTTGTCCAGGCTGGTTTCAAACTTGTGGGCTCAAGCGATC TTTTGTAGAGACAGGATTTTGCCATGTTGTCCGGGCTGGTTTCAAACTTGTGGGCTCAAGCGATC T C FBXL5 Ensembl:ENSG00000118564 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1011801439 Functional Loss SNV dbSNP153 33..33 33 - - - 18279 RMVar_ID_18279 Human_SNP_ID_174719763 A-to-I Human chr4 - 15673434 15673434 15673434 ATCCTTATTTTATCTTTATTTTTTTTGAGATGAGGTCTCACTCTGTTGCCCAGGGTGGAGTAGAG ATCCTTATTTTATCTTTATTTTTTTTGAGATGGGGTCTCACTCTGTTGCCCAGGGTGGAGTAGAG T C FBXL5 Ensembl:ENSG00000118564 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs148260009 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15082618 Clinvar_Rec_65 18280 RMVar_ID_18280 Human_SNP_ID_174980852 A-to-I Human chr4 - 16722829 16722829 16722829 TGAGGACTGTCTGGGCCTTCTTGCTGTTTCTCATCATGCCAAACAGACCCTACCCTCAGAACCTT TGAGGACTGTCTGGGCCTTCTTGCTGTTTCTCGTCATGCCAAACAGACCCTACCCTCAGAACCTT T C LDB2 Ensembl:ENSG00000169744 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs956604085 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55880,RMVar_hsa_circ_224950,RMVar_hsa_circ_14079,RMVar_hsa_circ_61130,RMVar_hsa_circ_376565,RMVar_hsa_circ_275757,RMVar_hsa_circ_224951,RMVar_hsa_circ_68927,RMVar_hsa_circ_317065,RMVar_hsa_circ_355422 18281 RMVar_ID_18281 Human_SNP_ID_174986118 A-to-I Human chr4 - 16743197 16743197 16743197 CAAACTCCGCCTCCTGGGTTCAAGCAATTCTCATGCCTCAGCCTCCTGAGTAGCTGGGATTACAG CAAACTCCGCCTCCTGGGTTCAAGCAATTCTCTTGCCTCAGCCTCCTGAGTAGCTGGGATTACAG T A LDB2 Ensembl:ENSG00000169744 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs141979448 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55880,RMVar_hsa_circ_224950,RMVar_hsa_circ_14079,RMVar_hsa_circ_61130,RMVar_hsa_circ_376565,RMVar_hsa_circ_275757,RMVar_hsa_circ_224951,RMVar_hsa_circ_68927,RMVar_hsa_circ_317065,RMVar_hsa_circ_355422 18282 RMVar_ID_18282 Human_SNP_ID_174987007 A-to-I Human chr4 - 16746671 16746671 16746671 GTGATTCTCCTGCCTCAGCCTCCTGAGTAGCCAGGACTACAGGCGCGTGCCACCATGCCCAGCTA GTGATTCTCCTGCCTCAGCCTCCTGAGTAGCCGGGACTACAGGCGCGTGCCACCATGCCCAGCTA T C LDB2 Ensembl:ENSG00000169744 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1214995168 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55880,RMVar_hsa_circ_224950,RMVar_hsa_circ_14079,RMVar_hsa_circ_61130,RMVar_hsa_circ_376565,RMVar_hsa_circ_275757,RMVar_hsa_circ_224951,RMVar_hsa_circ_68927,RMVar_hsa_circ_317065,RMVar_hsa_circ_355422 18283 RMVar_ID_18283 Human_SNP_ID_175171128 A-to-I Human chr4 - 17492316 17492316 17492316 TTTCCCAGGTATGATCGGGTACGGCATGGCCAAGGGTGCTGTTCACCAGCTCTGCCAGAGCCTGG TTTCCCAGGTATGATCGGGTACGGCATGGCCACGGGTGCTGTTCACCAGCTCTGCCAGAGCCTGG T G QDPR Ensembl:ENSG00000151552 Protein coding intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs760872904 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_616864,Human_RBP_ID_942578,Human_RBP_ID_1069379,Human_RBP_ID_4795344,Human_RBP_ID_22457848 Human_Splice_Rec_548718,Human_Splice_Rec_548719,Human_Splice_Rec_548738,Human_Splice_Rec_548739,Human_Splice_Rec_548743,Human_Splice_Rec_548775 RMVar_hsa_circ_54463,RMVar_hsa_circ_121417,RMVar_hsa_circ_53025,RMVar_hsa_circ_98341,RMVar_hsa_circ_224966,RMVar_hsa_circ_224967 18284 RMVar_ID_18284 Human_SNP_ID_175172102 A-to-I Human chr4 - 17496345 17496345 17496345 CTGACTCCTGGTTCAAGCAATTCTGCTGCCTCAGCCTCTGGAGCAGCTGGGATTACAGGCATGCA CTGACTCCTGGTTCAAGCAATTCTGCTGCCTCGGCCTCTGGAGCAGCTGGGATTACAGGCATGCA T C QDPR Ensembl:ENSG00000151552 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992139694 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54463,RMVar_hsa_circ_121417,RMVar_hsa_circ_53025,RMVar_hsa_circ_98341,RMVar_hsa_circ_224966,RMVar_hsa_circ_224967 18285 RMVar_ID_18285 Human_SNP_ID_175172104 A-to-I Human chr4 - 17496359 17496359 17496359 GCTCACCGCAACGTCTGACTCCTGGTTCAAGCAATTCTGCTGCCTCAGCCTCTGGAGCAGCTGGG GCTCACCGCAACGTCTGACTCCTGGTTCAAGCTATTCTGCTGCCTCAGCCTCTGGAGCAGCTGGG T A QDPR Ensembl:ENSG00000151552 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1470563985 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54463,RMVar_hsa_circ_121417,RMVar_hsa_circ_53025,RMVar_hsa_circ_98341,RMVar_hsa_circ_224966,RMVar_hsa_circ_224967 18286 RMVar_ID_18286 Human_SNP_ID_175173037 A-to-I Human chr4 - 17500098 17500098 17500098 ACAAAAAATTAGCCAGGCGTGATGGTGGCTGAAGCAGGAGAATGGCGTGAACCCAGGAGGTGGAG ACAAAAAATTAGCCAGGCGTGATGGTGGCTGAGGCAGGAGAATGGCGTGAACCCAGGAGGTGGAG T C QDPR Ensembl:ENSG00000151552 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1437855120 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54463,RMVar_hsa_circ_121417,RMVar_hsa_circ_53025,RMVar_hsa_circ_98341,RMVar_hsa_circ_224966,RMVar_hsa_circ_224967 18287 RMVar_ID_18287 Human_SNP_ID_175174388 A-to-I Human chr4 - 17505542 17505542 17505542 CAGCCTGATTTAAATCTTAAGAAGATTGGGCCAGGCGTGGTAGCTCAGTCCTGTTGTCCCAGCAC CAGCCTGATTTAAATCTTAAGAAGATTGGGCCCGGCGTGGTAGCTCAGTCCTGTTGTCCCAGCAC T G QDPR Ensembl:ENSG00000151552 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs895198786 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98341,RMVar_hsa_circ_224966,RMVar_hsa_circ_284056,RMVar_hsa_circ_224969,RMVar_hsa_circ_224970,RMVar_hsa_circ_364438 18288 RMVar_ID_18288 Human_SNP_ID_175175318 A-to-I Human chr4 - 17509318 17509318 17509318 TTGATGTGGTGGAGAATGAAGAGGCCAGCGCTAGCATCATTGTTAAAATGACAGACTCGTTCACT TTGATGTGGTGGAGAATGAAGAGGCCAGCGCTGGCATCATTGTTAAAATGACAGACTCGTTCACT T C QDPR Ensembl:ENSG00000151552 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1353342221 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24045382 Human_Splice_Rec_548700,Human_Splice_Rec_548701,Human_Splice_Rec_548712,Human_Splice_Rec_548713,Human_Splice_Rec_548724,Human_Splice_Rec_548725,Human_Splice_Rec_548748,Human_Splice_Rec_548749,Human_Splice_Rec_548758,Human_Splice_Rec_548759,Human_Splice_Rec_548768,Human_Splice_Rec_548769 RMVar_hsa_circ_98341,RMVar_hsa_circ_224966,RMVar_hsa_circ_284056,RMVar_hsa_circ_224969,RMVar_hsa_circ_224970,RMVar_hsa_circ_364438 18289 RMVar_ID_18289 Human_SNP_ID_175197929 A-to-I Human chr4 + 17595034 17595034 17595034 ATAAAATGAGCTAAAGGCTGGGCGCGATGGCTAATGCCTGTAATCCCAGCACTTTGGGAGGCCGA ATAAAATGAGCTAAAGGCTGGGCGCGATGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCGA A C LAP3 Ensembl:ENSG00000002549 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1364670427 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_52402,RMVar_hsa_circ_120628,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_224976,RMVar_hsa_circ_125968,RMVar_hsa_circ_59479,RMVar_hsa_circ_103612,RMVar_hsa_circ_224977,RMVar_hsa_circ_122741,RMVar_hsa_circ_224978,RMVar_hsa_circ_59283,RMVar_hsa_circ_224980,RMVar_hsa_circ_99452,RMVar_hsa_circ_224981 18290 RMVar_ID_18290 Human_SNP_ID_175198893 A-to-I Human chr4 + 17598784 17598784 17598784 CAAGCTGTACTTTTTTTTTGAGACGGAGTGTCACTCTGTCATCCAGGCTGGAGTGCAGTGGCGTG CAAGCTGTACTTTTTTTTTGAGACGGAGTGTCCCTCTGTCATCCAGGCTGGAGTGCAGTGGCGTG A C LAP3 Ensembl:ENSG00000002549 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1008721935 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120628,RMVar_hsa_circ_101194,RMVar_hsa_circ_224971,RMVar_hsa_circ_224974,RMVar_hsa_circ_122089,RMVar_hsa_circ_224976,RMVar_hsa_circ_125968,RMVar_hsa_circ_59479,RMVar_hsa_circ_103612,RMVar_hsa_circ_224977,RMVar_hsa_circ_122741,RMVar_hsa_circ_224978,RMVar_hsa_circ_224980,RMVar_hsa_circ_99452,RMVar_hsa_circ_89535,RMVar_hsa_circ_224981,RMVar_hsa_circ_224982 18291 RMVar_ID_18291 Human_SNP_ID_175198934 A-to-I Human chr4 + 17598943 17598943 17598943 ATTTTTAGTAGAGACGGGGTTTTTGCCATGTTAGCCAGGCTGGTTTCGAACTCCTGAACTCAGGT ATTTTTAGTAGAGACGGGGTTTTTGCCATGTTGGCCAGGCTGGTTTCGAACTCCTGAACTCAGGT A G LAP3 Ensembl:ENSG00000002549 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1164856023 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120628,RMVar_hsa_circ_101194,RMVar_hsa_circ_224971,RMVar_hsa_circ_224974,RMVar_hsa_circ_122089,RMVar_hsa_circ_224976,RMVar_hsa_circ_125968,RMVar_hsa_circ_59479,RMVar_hsa_circ_103612,RMVar_hsa_circ_224977,RMVar_hsa_circ_122741,RMVar_hsa_circ_224978,RMVar_hsa_circ_224980,RMVar_hsa_circ_99452,RMVar_hsa_circ_89535,RMVar_hsa_circ_224981,RMVar_hsa_circ_224982 18292 RMVar_ID_18292 Human_SNP_ID_175198963 A-to-I Human chr4 + 17599046 17599046 17599046 AGGCATGAGTCACTGTGCCTGGCCTAATTTTTATATTTTAGTAGAGATGGGGTTTAACCATGTTG AGGCATGAGTCACTGTGCCTGGCCTAATTTTTCTATTTTAGTAGAGATGGGGTTTAACCATGTTG A C LAP3 Ensembl:ENSG00000002549 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs912901259 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120628,RMVar_hsa_circ_101194,RMVar_hsa_circ_224971,RMVar_hsa_circ_224974,RMVar_hsa_circ_122089,RMVar_hsa_circ_224976,RMVar_hsa_circ_125968,RMVar_hsa_circ_59479,RMVar_hsa_circ_103612,RMVar_hsa_circ_224977,RMVar_hsa_circ_122741,RMVar_hsa_circ_224978,RMVar_hsa_circ_224980,RMVar_hsa_circ_99452,RMVar_hsa_circ_89535,RMVar_hsa_circ_224981,RMVar_hsa_circ_224982 18293 RMVar_ID_18293 Human_SNP_ID_175198967 A-to-I Human chr4 + 17599056 17599056 17599056 CACTGTGCCTGGCCTAATTTTTATATTTTAGTAGAGATGGGGTTTAACCATGTTGGCCGGGCTGG CACTGTGCCTGGCCTAATTTTTATATTTTAGTGGAGATGGGGTTTAACCATGTTGGCCGGGCTGG A G LAP3 Ensembl:ENSG00000002549 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1274955897 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120628,RMVar_hsa_circ_101194,RMVar_hsa_circ_224971,RMVar_hsa_circ_224974,RMVar_hsa_circ_122089,RMVar_hsa_circ_224976,RMVar_hsa_circ_125968,RMVar_hsa_circ_59479,RMVar_hsa_circ_103612,RMVar_hsa_circ_224977,RMVar_hsa_circ_122741,RMVar_hsa_circ_224978,RMVar_hsa_circ_224980,RMVar_hsa_circ_99452,RMVar_hsa_circ_89535,RMVar_hsa_circ_224981,RMVar_hsa_circ_224982 18294 RMVar_ID_18294 Human_SNP_ID_175198980 A-to-I Human chr4 + 17599124 17599124 17599124 CAAACTCCTGACCAAGGTGATTCACCTGTCTCAGCCTCCCAAAGTGCTGGGATTACAAGATTACA CAAACTCCTGACCAAGGTGATTCACCTGTCTCTGCCTCCCAAAGTGCTGGGATTACAAGATTACA A T LAP3 Ensembl:ENSG00000002549 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1284277992 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120628,RMVar_hsa_circ_101194,RMVar_hsa_circ_224971,RMVar_hsa_circ_224974,RMVar_hsa_circ_122089,RMVar_hsa_circ_224976,RMVar_hsa_circ_125968,RMVar_hsa_circ_59479,RMVar_hsa_circ_103612,RMVar_hsa_circ_224977,RMVar_hsa_circ_122741,RMVar_hsa_circ_224978,RMVar_hsa_circ_224980,RMVar_hsa_circ_99452,RMVar_hsa_circ_89535,RMVar_hsa_circ_224981,RMVar_hsa_circ_224982 18295 RMVar_ID_18295 Human_SNP_ID_175199753 A-to-I Human chr4 + 17602746 17602743 17602746 GAGTCTCACTCTGTTGCCCAGGCTGCAGTGGCACGATCTCAGCTCACTGCAGCCTCTGCCTCCTG GAGTCTCACTCTGTTGCCCAGGCTGCAGTG___CGATCTCAGCTCACTGCAGCCTCTGCCTCCTG GGCA G LAP3 Ensembl:ENSG00000002549 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1258806920 Functional Loss DEL dbSNP153 31..33 33 - - - RMVar_hsa_circ_120628,RMVar_hsa_circ_101194,RMVar_hsa_circ_224971,RMVar_hsa_circ_224974,RMVar_hsa_circ_122089,RMVar_hsa_circ_224976,RMVar_hsa_circ_125968,RMVar_hsa_circ_59479,RMVar_hsa_circ_103612,RMVar_hsa_circ_224977,RMVar_hsa_circ_122741,RMVar_hsa_circ_224978,RMVar_hsa_circ_224980,RMVar_hsa_circ_99452,RMVar_hsa_circ_89535,RMVar_hsa_circ_224981,RMVar_hsa_circ_224982 18296 RMVar_ID_18296 Human_SNP_ID_175199761 A-to-I Human chr4 + 17602784 17602784 17602784 TCAGCTCACTGCAGCCTCTGCCTCCTGGGTTCAAGCCATTCTCCTGCCTCAGCCACCTGAGTAGC TCAGCTCACTGCAGCCTCTGCCTCCTGGGTTCCAGCCATTCTCCTGCCTCAGCCACCTGAGTAGC A C LAP3 Ensembl:ENSG00000002549 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs962624437 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120628,RMVar_hsa_circ_101194,RMVar_hsa_circ_224971,RMVar_hsa_circ_224974,RMVar_hsa_circ_122089,RMVar_hsa_circ_224976,RMVar_hsa_circ_125968,RMVar_hsa_circ_59479,RMVar_hsa_circ_103612,RMVar_hsa_circ_224977,RMVar_hsa_circ_122741,RMVar_hsa_circ_224978,RMVar_hsa_circ_224980,RMVar_hsa_circ_99452,RMVar_hsa_circ_89535,RMVar_hsa_circ_224981,RMVar_hsa_circ_224982 18297 RMVar_ID_18297 Human_SNP_ID_175199782 A-to-I Human chr4 + 17602865 17602865 17602865 CGCCACCACACTCGGATTTTTGTATTTTTAGTAGAGACGGGGTTTCACAGTGTTGGTCAGGCTGG CGCCACCACACTCGGATTTTTGTATTTTTAGTGGAGACGGGGTTTCACAGTGTTGGTCAGGCTGG A G LAP3 Ensembl:ENSG00000002549 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1193675005 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120628,RMVar_hsa_circ_101194,RMVar_hsa_circ_224971,RMVar_hsa_circ_224974,RMVar_hsa_circ_122089,RMVar_hsa_circ_224976,RMVar_hsa_circ_125968,RMVar_hsa_circ_59479,RMVar_hsa_circ_103612,RMVar_hsa_circ_224977,RMVar_hsa_circ_122741,RMVar_hsa_circ_224978,RMVar_hsa_circ_224980,RMVar_hsa_circ_99452,RMVar_hsa_circ_89535,RMVar_hsa_circ_224981,RMVar_hsa_circ_224982 18298 RMVar_ID_18298 Human_SNP_ID_175199800 A-to-I Human chr4 + 17602943 17602943 17602943 ACCTCAAGTGATCCACCCGTCTCAGCCTCCCAAAATGCTGGGATTACAGGTGTGAGCCACCGCGC ACCTCAAGTGATCCACCCGTCTCAGCCTCCCACAATGCTGGGATTACAGGTGTGAGCCACCGCGC A C LAP3 Ensembl:ENSG00000002549 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs973346995 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120628,RMVar_hsa_circ_101194,RMVar_hsa_circ_224971,RMVar_hsa_circ_224974,RMVar_hsa_circ_122089,RMVar_hsa_circ_224976,RMVar_hsa_circ_125968,RMVar_hsa_circ_59479,RMVar_hsa_circ_103612,RMVar_hsa_circ_224977,RMVar_hsa_circ_122741,RMVar_hsa_circ_224978,RMVar_hsa_circ_224980,RMVar_hsa_circ_99452,RMVar_hsa_circ_89535,RMVar_hsa_circ_224981,RMVar_hsa_circ_224982 18299 RMVar_ID_18299 Human_SNP_ID_175199900 A-to-I Human chr4 + 17603295 17603295 17603295 GCACCACTGCACTCCAGCCTGGGCAACAGAGCAAGACTCTGTCTCAAAAAAGGAGGAACACATGC GCACCACTGCACTCCAGCCTGGGCAACAGAGCTAGACTCTGTCTCAAAAAAGGAGGAACACATGC A T LAP3 Ensembl:ENSG00000002549 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1397741626 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120628,RMVar_hsa_circ_101194,RMVar_hsa_circ_224971,RMVar_hsa_circ_224974,RMVar_hsa_circ_122089,RMVar_hsa_circ_224976,RMVar_hsa_circ_125968,RMVar_hsa_circ_59479,RMVar_hsa_circ_103612,RMVar_hsa_circ_224977,RMVar_hsa_circ_122741,RMVar_hsa_circ_224978,RMVar_hsa_circ_224980,RMVar_hsa_circ_99452,RMVar_hsa_circ_89535,RMVar_hsa_circ_224981,RMVar_hsa_circ_224982 18300 RMVar_ID_18300 Human_SNP_ID_175200111 A-to-I Human chr4 + 17603945 17603945 17603945 GCCTCCTGGGTTCAAGCAATTCTCCCTATCTCAGCCTCCTGAGTAGCTGGGATTACAGGCACCAC GCCTCCTGGGTTCAAGCAATTCTCCCTATCTCGGCCTCCTGAGTAGCTGGGATTACAGGCACCAC A G LAP3 Ensembl:ENSG00000002549 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1560152701 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120628,RMVar_hsa_circ_101194,RMVar_hsa_circ_224971,RMVar_hsa_circ_224974,RMVar_hsa_circ_122089,RMVar_hsa_circ_224976,RMVar_hsa_circ_125968,RMVar_hsa_circ_59479,RMVar_hsa_circ_103612,RMVar_hsa_circ_224977,RMVar_hsa_circ_122741,RMVar_hsa_circ_224978,RMVar_hsa_circ_224980,RMVar_hsa_circ_99452,RMVar_hsa_circ_89535,RMVar_hsa_circ_224981,RMVar_hsa_circ_224982 18301 RMVar_ID_18301 Human_SNP_ID_175200179 A-to-I Human chr4 + 17604239 17604239 17604239 GGCTGCATACAGTGAGCTCTGATCATACCACTACACTGCAGCCTGGGTGAGTGAGACCTTTCTCA GGCTGCATACAGTGAGCTCTGATCATACCACTGCACTGCAGCCTGGGTGAGTGAGACCTTTCTCA A G LAP3 Ensembl:ENSG00000002549 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1245529484 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25791933 RMVar_hsa_circ_120628,RMVar_hsa_circ_101194,RMVar_hsa_circ_224971,RMVar_hsa_circ_224974,RMVar_hsa_circ_122089,RMVar_hsa_circ_224976,RMVar_hsa_circ_125968,RMVar_hsa_circ_59479,RMVar_hsa_circ_103612,RMVar_hsa_circ_224977,RMVar_hsa_circ_122741,RMVar_hsa_circ_224978,RMVar_hsa_circ_224980,RMVar_hsa_circ_99452,RMVar_hsa_circ_89535,RMVar_hsa_circ_224981,RMVar_hsa_circ_224982 18302 RMVar_ID_18302 Human_SNP_ID_175202134 A-to-I Human chr4 - 17611704 17611704 17611704 ACAATTACAGCTCACCATAACTTCCGCCTCCCAGGCTCCAGCAATTCTCCCAATCAGCCTCCCAA ACAATTACAGCTCACCATAACTTCCGCCTCCCGGGCTCCAGCAATTCTCCCAATCAGCCTCCCAA T C AC006160.1 Ensembl:ENSG00000249502 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs370331138 Functional Loss SNV dbSNP153 33..33 33 - - - 18303 RMVar_ID_18303 Human_SNP_ID_175206739 A-to-I Human chr4 + 17626100 17626100 17626100 TGCAGATTAAAGGAGATGTTGAGGCCAGGTGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGG TGCAGATTAAAGGAGATGTTGAGGCCAGGTGCCGTGGCTCACGCCTGTAATCCCAGCACTTTGGG A C MED28 Ensembl:ENSG00000118579 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs965831566 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15098703 18304 RMVar_ID_18304 Human_SNP_ID_175206740 A-to-I Human chr4 + 17626100 17626100 17626100 TGCAGATTAAAGGAGATGTTGAGGCCAGGTGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGG TGCAGATTAAAGGAGATGTTGAGGCCAGGTGCTGTGGCTCACGCCTGTAATCCCAGCACTTTGGG A T MED28 Ensembl:ENSG00000118579 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs965831566 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15098703 18305 RMVar_ID_18305 Human_SNP_ID_175206754 A-to-I Human chr4 + 17626146 17626146 17626146 GTAATCCCAGCACTTTGGGGGGCTGAGGCAGGAGAATCGCTTGAACCTGGGAGGCAGAGGTTGTG GTAATCCCAGCACTTTGGGGGGCTGAGGCAGGGGAATCGCTTGAACCTGGGAGGCAGAGGTTGTG A G MED28 Ensembl:ENSG00000118579 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs563728252 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7288888 18306 RMVar_ID_18306 Human_SNP_ID_175206765 A-to-I Human chr4 + 17626186 17626186 17626186 TTGAACCTGGGAGGCAGAGGTTGTGATGAGCCAAGATCGTGCCATTGCACTCCATCCTGGGCTAC TTGAACCTGGGAGGCAGAGGTTGTGATGAGCCGAGATCGTGCCATTGCACTCCATCCTGGGCTAC A G MED28 Ensembl:ENSG00000118579 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs559928684 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_617049 18307 RMVar_ID_18307 Human_SNP_ID_175207012 A-to-I Human chr4 + 17627076 17627076 17627076 ACCTCTGCCTCCCGGGTTCAAGTAATTTTCCTACGTCAGCCTCCCGAGTAGCTGTCAGGTGCACA ACCTCTGCCTCCCGGGTTCAAGTAATTTTCCTGCGTCAGCCTCCCGAGTAGCTGTCAGGTGCACA A G MED28 Ensembl:ENSG00000118579 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1040584859 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15098763,Human_RBP_ID_24045767 18308 RMVar_ID_18308 Human_SNP_ID_175207598 A-to-I Human chr4 + 17628930 17628929 17628931 AAGATAAGAGGAGTACTGCACACAAGGACAGTAGAGTGTCTGTTCCCTGCAGAGGGATAGTGAGG AAGATAAGAGGAGTACTGCACACAAGGACAGT__AGTGTCTGTTCCCTGCAGAGGGATAGTGAGG TAG T MED28 Ensembl:ENSG00000118579 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1309524733 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_15098837,Human_RBP_ID_24045809 RMVar_hsa_circ_224985 18309 RMVar_ID_18309 Human_SNP_ID_175207599 A-to-I Human chr4 + 17628930 17628930 17628930 AAGATAAGAGGAGTACTGCACACAAGGACAGTAGAGTGTCTGTTCCCTGCAGAGGGATAGTGAGG AAGATAAGAGGAGTACTGCACACAAGGACAGTCGAGTGTCTGTTCCCTGCAGAGGGATAGTGAGG A C MED28 Ensembl:ENSG00000118579 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs571820173 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15098837,Human_RBP_ID_24045809 RMVar_hsa_circ_224985 18310 RMVar_ID_18310 Human_SNP_ID_175207600 A-to-I Human chr4 + 17628930 17628930 17628930 AAGATAAGAGGAGTACTGCACACAAGGACAGTAGAGTGTCTGTTCCCTGCAGAGGGATAGTGAGG AAGATAAGAGGAGTACTGCACACAAGGACAGTGGAGTGTCTGTTCCCTGCAGAGGGATAGTGAGG A G MED28 Ensembl:ENSG00000118579 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs571820173 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15098837,Human_RBP_ID_24045809 RMVar_hsa_circ_224985 18311 RMVar_ID_18311 Human_SNP_ID_175208687 A-to-I Human chr4 + 17632258 17632258 17632258 CACCATGCCTGGCTAATTTTTGTATATTTTGTAGAGATGGGGTTTCACCATATTGGCCAGGCTGG CACCATGCCTGGCTAATTTTTGTATATTTTGTGGAGATGGGGTTTCACCATATTGGCCAGGCTGG A G MED28 Ensembl:ENSG00000118579 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1560161636 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15098995 18312 RMVar_ID_18312 Human_SNP_ID_175208693 A-to-I Human chr4 + 17632277 17632277 17632277 TTGTATATTTTGTAGAGATGGGGTTTCACCATATTGGCCAGGCTGGTCTCAAATTCCTGGACTCA TTGTATATTTTGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTCAAATTCCTGGACTCA A G MED28 Ensembl:ENSG00000118579 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs566398609 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15098995 18313 RMVar_ID_18313 Human_SNP_ID_175208694 A-to-I Human chr4 + 17632277 17632277 17632277 TTGTATATTTTGTAGAGATGGGGTTTCACCATATTGGCCAGGCTGGTCTCAAATTCCTGGACTCA TTGTATATTTTGTAGAGATGGGGTTTCACCATTTTGGCCAGGCTGGTCTCAAATTCCTGGACTCA A T MED28 Ensembl:ENSG00000118579 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs566398609 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15098995 18314 RMVar_ID_18314 Human_SNP_ID_175208923 A-to-I Human chr4 + 17632996 17632996 17632996 CAGGCTGGAGTGCAGTGGCATGATCTCGGCTCACTGCAACCTCCAGCCTCCTGCGTTCAAGCGAT CAGGCTGGAGTGCAGTGGCATGATCTCGGCTCGCTGCAACCTCCAGCCTCCTGCGTTCAAGCGAT A G MED28 Ensembl:ENSG00000118579 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1039226904 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3733423,Human_RBP_ID_7288960,Human_RBP_ID_15099027 18315 RMVar_ID_18315 Human_SNP_ID_175209967 A-to-I Human chr4 + 17636223 17636223 17636223 TGTCTCTCGGGTTCAAGTGATTCTCCTGCCTCAGCCTTCCTAGAAGCTGGAATTACAGATGCCCA TGTCTCTCGGGTTCAAGTGATTCTCCTGCCTCGGCCTTCCTAGAAGCTGGAATTACAGATGCCCA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1560163182 Functional Loss SNV dbSNP153 33..33 33 - - - 18316 RMVar_ID_18316 Human_SNP_ID_175251792 A-to-I Human chr4 - 17801204 17801204 17801204 GAATTGCTTGAACCTGGGAGGTGGAGGTTGCAATGAGCTGAGATCGCGCCACTGCACTCCAGCCT GAATTGCTTGAACCTGGGAGGTGGAGGTTGCAGTGAGCTGAGATCGCGCCACTGCACTCCAGCCT T C DCAF16 Ensembl:ENSG00000163257 Protein coding 3'UTR GSE47997;GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,24183664,31158229,31158229 RNA-Seq:(High) rs1250058464 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25792319,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 18317 RMVar_ID_18317 Human_SNP_ID_175251796 A-to-I Human chr4 - 17801225 17801225 17801225 ACTTGGGAGGCTAAGACAGGAGAATTGCTTGAACCTGGGAGGTGGAGGTTGCAATGAGCTGAGAT ACTTGGGAGGCTAAGACAGGAGAATTGCTTGACCCTGGGAGGTGGAGGTTGCAATGAGCTGAGAT T G DCAF16 Ensembl:ENSG00000163257 Protein coding 3'UTR GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,29796672,31158229,31158229 RNA-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 18318 RMVar_ID_18318 Human_SNP_ID_175251804 A-to-I Human chr4 - 17801257 17801257 17801257 GGGCGTGGTGGCATGTGCCTGTAATCGCAGCTACTTGGGAGGCTAAGACAGGAGAATTGCTTGAA GGGCGTGGTGGCATGTGCCTGTAATCGCAGCTGCTTGGGAGGCTAAGACAGGAGAATTGCTTGAA T C DCAF16 Ensembl:ENSG00000163257 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs933450984 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 18319 RMVar_ID_18319 Human_SNP_ID_175251819 A-to-I Human chr4 - 17801307 17801307 17801307 CTGGCCAACATGGTGAAAGCCCATCTCTACTAAAAATATAAAAATTAGCCGGGCGTGGTGGCATG CTGGCCAACATGGTGAAAGCCCATCTCTACTAGAAATATAAAAATTAGCCGGGCGTGGTGGCATG T C DCAF16 Ensembl:ENSG00000163257 Protein coding 3'UTR GSE47997;GSE38233;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,29796672,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs1246449767 Functional Loss SNV dbSNP153 33..33 33 - - - 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 18320 RMVar_ID_18320 Human_SNP_ID_175251820 A-to-I Human chr4 - 17801308 17801308 17801308 CCTGGCCAACATGGTGAAAGCCCATCTCTACTAAAAATATAAAAATTAGCCGGGCGTGGTGGCAT CCTGGCCAACATGGTGAAAGCCCATCTCTACTGAAAATATAAAAATTAGCCGGGCGTGGTGGCAT T C DCAF16 Ensembl:ENSG00000163257 Protein coding 3'UTR GSE47997;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,29796672,31158229,32596459 RNA-Seq:(High) rs954477096 Functional Loss SNV dbSNP153 33..33 33 - - - 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 18321 RMVar_ID_18321 Human_SNP_ID_175251828 A-to-I Human chr4 - 17801332 17801332 17801332 TTGAGATCAGGAGTTCGTGACCAGCCTGGCCAACATGGTGAAAGCCCATCTCTACTAAAAATATA TTGAGATCAGGAGTTCGTGACCAGCCTGGCCAGCATGGTGAAAGCCCATCTCTACTAAAAATATA T C DCAF16 Ensembl:ENSG00000163257 Protein coding 3'UTR GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs186922846 Functional Loss SNV dbSNP153 33..33 33 - - - 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 18322 RMVar_ID_18322 Human_SNP_ID_175251831 A-to-I Human chr4 - 17801356 17801356 17801356 GGAGGCTGAGGGCAGGTGGATCACTTGAGATCAGGAGTTCGTGACCAGCCTGGCCAACATGGTGA GGAGGCTGAGGGCAGGTGGATCACTTGAGATCCGGAGTTCGTGACCAGCCTGGCCAACATGGTGA T G DCAF16 Ensembl:ENSG00000163257 Protein coding 3'UTR GSE38233;GSE100210;GSE99789;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;ASD brains,Fragile X samples from NIH NeuroBioBank;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,29796672,30559470,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs951382474 Functional Loss SNV dbSNP153 33..33 33 - - - 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 18323 RMVar_ID_18323 Human_SNP_ID_175251836 A-to-I Human chr4 - 17801386 17801386 17801386 GTGGCTCATGCCTGTAATCCCAACAGTTTGGGAGGCTGAGGGCAGGTGGATCACTTGAGATCAGG GTGGCTCATGCCTGTAATCCCAACAGTTTGGGTGGCTGAGGGCAGGTGGATCACTTGAGATCAGG T A DCAF16 Ensembl:ENSG00000163257 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs928674325 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7289929 Human_miRNA_ID_342949,Human_miRNA_ID_587006,Human_miRNA_ID_1695296,Human_miRNA_ID_2085369 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 18324 RMVar_ID_18324 Human_SNP_ID_175251842 A-to-I Human chr4 - 17801396 17801396 17801396 GCCAGGCATGGTGGCTCATGCCTGTAATCCCAACAGTTTGGGAGGCTGAGGGCAGGTGGATCACT GCCAGGCATGGTGGCTCATGCCTGTAATCCCAGCAGTTTGGGAGGCTGAGGGCAGGTGGATCACT T C DCAF16 Ensembl:ENSG00000163257 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1021965772 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7289929 Human_miRNA_ID_1316459,Human_miRNA_ID_2085369 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,RMVar_hsa_circ_224994 18325 RMVar_ID_18325 Human_SNP_ID_175251968 A-to-I Human chr4 - 17801914 17801914 17801914 TATTTTTAGTAGAGACAGGGTTTCACCGTGTTAGCCAGGATGGTCTTGATCTCCTGACCTCGTGA TATTTTTAGTAGAGACAGGGTTTCACCGTGTTGGCCAGGATGGTCTTGATCTCCTGACCTCGTGA T C DCAF16 Ensembl:ENSG00000163257 Protein coding 3'UTR GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1161203966 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_337665 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 18326 RMVar_ID_18326 Human_SNP_ID_175251978 A-to-I Human chr4 - 17801955 17801955 17801955 GGGACTACAGGCGTCCACCACCACTCCTGGCTATTTTTTTGTATTTTTAGTAGAGACAGGGTTTC GGGACTACAGGCGTCCACCACCACTCCTGGCTGTTTTTTTGTATTTTTAGTAGAGACAGGGTTTC T C DCAF16 Ensembl:ENSG00000163257 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1358560891 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_617377 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 18327 RMVar_ID_18327 Human_SNP_ID_175251983 A-to-I Human chr4 - 17801981 17801981 17801981 TCTCCTGCCCTGCCTCCCGAATAGCTGGGACTACAGGCGTCCACCACCACTCCTGGCTATTTTTT TCTCCTGCCCTGCCTCCCGAATAGCTGGGACTGCAGGCGTCCACCACCACTCCTGGCTATTTTTT T C DCAF16 Ensembl:ENSG00000163257 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE99789;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,29129909,29796672,30559470,31158229,31158229,31158229,32596459,32596459 RNA-Seq:(High) rs1029737247 Functional Loss SNV dbSNP153 33..33 33 - - - 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 18328 RMVar_ID_18328 Human_SNP_ID_175251986 A-to-I Human chr4 - 17801993 17801993 17801993 GGTTCGTGCCATTCTCCTGCCCTGCCTCCCGAATAGCTGGGACTACAGGCGTCCACCACCACTCC GGTTCGTGCCATTCTCCTGCCCTGCCTCCCGAGTAGCTGGGACTACAGGCGTCCACCACCACTCC T C DCAF16 Ensembl:ENSG00000163257 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1342125516 Functional Loss SNV dbSNP153 33..33 33 - - - 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 18329 RMVar_ID_18329 Human_SNP_ID_175251987 A-to-I Human chr4 - 17801994 17801994 17801994 GGGTTCGTGCCATTCTCCTGCCCTGCCTCCCGAATAGCTGGGACTACAGGCGTCCACCACCACTC GGGTTCGTGCCATTCTCCTGCCCTGCCTCCCGGATAGCTGGGACTACAGGCGTCCACCACCACTC T C DCAF16 Ensembl:ENSG00000163257 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1210142952 Functional Loss SNV dbSNP153 33..33 33 - - - 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 18330 RMVar_ID_18330 Human_SNP_ID_175252274 A-to-I Human chr4 - 17803058 17803056 17803058 ATTATGCCACTGTACTCCAGCCTGGGTGACAGAGCGAGACTCAGTCTCAAAAAAAAAAAAGGAGA ATTATGCCACTGTACTCCAGCCTGGGTGACAG__CGAGACTCAGTCTCAAAAAAAAAAAAGGAGA GCT G DCAF16 Ensembl:ENSG00000163257 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1560209187 Functional Loss DEL dbSNP153 33..34 33 - - - 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 18331 RMVar_ID_18331 Human_SNP_ID_175252323 A-to-I Human chr4 - 17803224 17803224 17803224 AGTCAGAAGTTTGAGACCAGCCTTGCCAACACAGTGAAACCCTGTCTCTACTAAAAATAAAAAAA AGTCAGAAGTTTGAGACCAGCCTTGCCAACACTGTGAAACCCTGTCTCTACTAAAAATAAAAAAA T A DCAF16 Ensembl:ENSG00000163257 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs3178753 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1221290 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 18332 RMVar_ID_18332 Human_SNP_ID_175252324 A-to-I Human chr4 - 17803224 17803224 17803224 AGTCAGAAGTTTGAGACCAGCCTTGCCAACACAGTGAAACCCTGTCTCTACTAAAAATAAAAAAA AGTCAGAAGTTTGAGACCAGCCTTGCCAACACGGTGAAACCCTGTCTCTACTAAAAATAAAAAAA T C DCAF16 Ensembl:ENSG00000163257 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs3178753 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1221290 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 18333 RMVar_ID_18333 Human_SNP_ID_175252325 A-to-I Human chr4 - 17803228 17803228 17803228 CTGAAGTCAGAAGTTTGAGACCAGCCTTGCCAACACAGTGAAACCCTGTCTCTACTAAAAATAAA CTGAAGTCAGAAGTTTGAGACCAGCCTTGCCAGCACAGTGAAACCCTGTCTCTACTAAAAATAAA T C DCAF16 Ensembl:ENSG00000163257 Protein coding 3'UTR GSE47997;GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,29129909,31158229,32596459 RNA-Seq:(High) rs1168315312 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15101335 Human_miRNA_ID_140489,Human_miRNA_ID_417474,Human_miRNA_ID_1221290,Human_miRNA_ID_2131560 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 18334 RMVar_ID_18334 Human_SNP_ID_175252454 A-to-I Human chr4 - 17803656 17803656 17803656 CTAAGCCGAACATTGAGTAGAGCCACTCCCATACCTGAATACCTAAAACAGATCCCTAATTCATG CTAAGCCGAACATTGAGTAGAGCCACTCCCATGCCTGAATACCTAAAACAGATCCCTAATTCATG T C DCAF16 Ensembl:ENSG00000163257 Protein coding CDS GSE56152 embryonic stem cells,wild type - 25708366 RNA-Seq:(High) rs763467832 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15101357,Human_RBP_ID_17294199 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 18335 RMVar_ID_18335 Human_SNP_ID_175255420 A-to-I Human chr4 + 17815531 17815531 17815531 TATAGAAAACACAGGGCTAAAGATTTTGATATATATATATTTTTGAGACAGAGTCTCACTCTATC TATAGAAAACACAGGGCTAAAGATTTTGATATGTATATATTTTTGAGACAGAGTCTCACTCTATC A G NCAPG Ensembl:ENSG00000109805 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs534674682 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15101828 RMVar_hsa_circ_90367,RMVar_hsa_circ_23266,RMVar_hsa_circ_82819,RMVar_hsa_circ_367171,RMVar_hsa_circ_55362,RMVar_hsa_circ_224999,RMVar_hsa_circ_225000,RMVar_hsa_circ_335815,RMVar_hsa_circ_364543,RMVar_hsa_circ_124981,RMVar_hsa_circ_7142,RMVar_hsa_circ_225001,RMVar_hsa_circ_225002,RMVar_hsa_circ_292811,RMVar_hsa_circ_318990,RMVar_hsa_circ_113899,RMVar_hsa_circ_123846,RMVar_hsa_circ_106175,RMVar_hsa_circ_225003,RMVar_hsa_circ_225005,RMVar_hsa_circ_225006,RMVar_hsa_circ_225004,RMVar_hsa_circ_27912 18336 RMVar_ID_18336 Human_SNP_ID_175255421 A-to-I Human chr4 + 17815533 17815533 17815533 TAGAAAACACAGGGCTAAAGATTTTGATATATATATATTTTTGAGACAGAGTCTCACTCTATCAC TAGAAAACACAGGGCTAAAGATTTTGATATATTTATATTTTTGAGACAGAGTCTCACTCTATCAC A T NCAPG Ensembl:ENSG00000109805 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1560222176 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15101828 RMVar_hsa_circ_90367,RMVar_hsa_circ_23266,RMVar_hsa_circ_82819,RMVar_hsa_circ_367171,RMVar_hsa_circ_55362,RMVar_hsa_circ_224999,RMVar_hsa_circ_225000,RMVar_hsa_circ_335815,RMVar_hsa_circ_364543,RMVar_hsa_circ_124981,RMVar_hsa_circ_7142,RMVar_hsa_circ_225001,RMVar_hsa_circ_225002,RMVar_hsa_circ_292811,RMVar_hsa_circ_318990,RMVar_hsa_circ_113899,RMVar_hsa_circ_123846,RMVar_hsa_circ_106175,RMVar_hsa_circ_225003,RMVar_hsa_circ_225005,RMVar_hsa_circ_225006,RMVar_hsa_circ_225004,RMVar_hsa_circ_27912 18337 RMVar_ID_18337 Human_SNP_ID_175255432 A-to-I Human chr4 + 17815561 17815561 17815561 ATATATATATTTTTGAGACAGAGTCTCACTCTATCACCCAGACTGGAGTGCTGTGGTGCAATCTT ATATATATATTTTTGAGACAGAGTCTCACTCTGTCACCCAGACTGGAGTGCTGTGGTGCAATCTT A G NCAPG Ensembl:ENSG00000109805 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs566219796 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90367,RMVar_hsa_circ_23266,RMVar_hsa_circ_82819,RMVar_hsa_circ_367171,RMVar_hsa_circ_55362,RMVar_hsa_circ_224999,RMVar_hsa_circ_225000,RMVar_hsa_circ_335815,RMVar_hsa_circ_364543,RMVar_hsa_circ_124981,RMVar_hsa_circ_7142,RMVar_hsa_circ_225001,RMVar_hsa_circ_225002,RMVar_hsa_circ_292811,RMVar_hsa_circ_318990,RMVar_hsa_circ_113899,RMVar_hsa_circ_123846,RMVar_hsa_circ_106175,RMVar_hsa_circ_225003,RMVar_hsa_circ_225005,RMVar_hsa_circ_225006,RMVar_hsa_circ_225004,RMVar_hsa_circ_27912 18338 RMVar_ID_18338 Human_SNP_ID_175270542 A-to-I Human chr4 - 17881159 17881158 17881159 TGTTCCTCAAGTATTTTATATTAAAAAAAAAAAGAAGGAAAAGAGAAAACAGTGCCTCTGTTTTT TGTTCCTCAAGTATTTTATATTAAAAAAAAAA_GAAGGAAAAGAGAAAACAGTGCCTCTGTTTTT CT C LCORL Ensembl:ENSG00000178177 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs878999700 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_225014,RMVar_hsa_circ_44699,RMVar_hsa_circ_351319,RMVar_hsa_circ_23965,RMVar_hsa_circ_225015 18339 RMVar_ID_18339 Human_SNP_ID_175304506 A-to-I Human chr4 - 18019229 18019229 18019229 ATTCAAGCGATTCTCCTGCCTGAGCCTCCCGAATAGTTGGGATTACAGGCGTCCGCCACCACGCC ATTCAAGCGATTCTCCTGCCTGAGCCTCCCGAGTAGTTGGGATTACAGGCGTCCGCCACCACGCC T C LCORL Ensembl:ENSG00000178177 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs951652235 Functional Loss SNV dbSNP153 33..33 33 - - - 18340 RMVar_ID_18340 Human_SNP_ID_175869918 A-to-I Human chr4 + 20281016 20281016 20281016 CACCACGCCCGGCTGATTTTTGTGTTTTTAGTAGAGATGGGGTTTCTCCATGTTGGTCAGGCTGG CACCACGCCCGGCTGATTTTTGTGTTTTTAGTGGAGATGGGGTTTCTCCATGTTGGTCAGGCTGG A G SLIT2 Ensembl:ENSG00000145147 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs534489266 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10138830,Human_RBP_ID_15119030,Human_RBP_ID_23030558,Human_RBP_ID_25832869 RMVar_hsa_circ_119829,RMVar_hsa_circ_76009,RMVar_hsa_circ_99485,RMVar_hsa_circ_225029,RMVar_hsa_circ_225030,RMVar_hsa_circ_109170,RMVar_hsa_circ_225033,RMVar_hsa_circ_225035 18341 RMVar_ID_18341 Human_SNP_ID_175993411 A-to-I Human chr4 + 20752248 20752248 20752248 GCCCGGCGAATTTTTGTATGTTTAGTAGAGACAGGGTTTCATCACGTTGGCCAGACTGGTCTCGA GCCCGGCGAATTTTTGTATGTTTAGTAGAGACGGGGTTTCATCACGTTGGCCAGACTGGTCTCGA A G PACRGL Ensembl:ENSG00000163138 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs779070384 Functional Loss SNV dbSNP153 33..33 33 - - - 18342 RMVar_ID_18342 Human_SNP_ID_176064154 A-to-I Human chr4 - 21026451 21026451 21026451 AGGGGTTTCACCTTGTTGCCCCAGCTGGTCTCAAACTCCTGGGTTCAACCGAGCAAACTAACTTG AGGGGTTTCACCTTGTTGCCCCAGCTGGTCTCCAACTCCTGGGTTCAACCGAGCAAACTAACTTG T G KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs769418281 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16582 18343 RMVar_ID_18343 Human_SNP_ID_176083442 A-to-I Human chr4 - 21099394 21099394 21099394 GTCCATGTGTTCTCATCATTCAGCTCCCACATAAAAGTGAGAACATGCGGTGTTTGGTTTTCTGT GTCCATGTGTTCTCATCATTCAGCTCCCACATGAAAGTGAGAACATGCGGTGTTTGGTTTTCTGT T C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1375918820 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16582 18344 RMVar_ID_18344 Human_SNP_ID_176089944 A-to-I Human chr4 - 21120487 21120487 21120487 CTTCCCCAGCCATGCAGAACTGTGAGTCAAATAAACCTCTTTCCTTTATAAATTACCCAGTCTGG CTTCCCCAGCCATGCAGAACTGTGAGTCAAATGAACCTCTTTCCTTTATAAATTACCCAGTCTGG T C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1358411735 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16582 18345 RMVar_ID_18345 Human_SNP_ID_176089953 A-to-I Human chr4 - 21120521 21120521 21120521 TTCACCTTCCACCATGATTATAAGTTGCCTGAAGCTTCCCCAGCCATGCAGAACTGTGAGTCAAA TTCACCTTCCACCATGATTATAAGTTGCCTGACGCTTCCCCAGCCATGCAGAACTGTGAGTCAAA T G KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs919530773 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16582 18346 RMVar_ID_18346 Human_SNP_ID_176105331 A-to-I Human chr4 - 21183598 21183598 21183598 ACTGGCAGATATGTGGAAAAAAGGAGGACCCTAGTACACTTTTGGTGGAAATATAAATTACAGCC ACTGGCAGATATGTGGAAAAAAGGAGGACCCTCGTACACTTTTGGTGGAAATATAAATTACAGCC T G KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1018369828 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16582 18347 RMVar_ID_18347 Human_SNP_ID_176108781 A-to-I Human chr4 - 21197180 21197180 21197180 GCAATAGTTAATATTCACAATAACCAAATATTAGAAACAACCCAGACACCCACTGCAATAGAATG GCAATAGTTAATATTCACAATAACCAAATATTGGAAACAACCCAGACACCCACTGCAATAGAATG T C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1354067821 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16582 18348 RMVar_ID_18348 Human_SNP_ID_176113408 A-to-I Human chr4 - 21215890 21215890 21215890 GATGGCTTGGGCTAGGAGGTTGAGGCTGCAGTAGGCCATGGAGGATCCACTACACTCCAGCCTGG GATGGCTTGGGCTAGGAGGTTGAGGCTGCAGTGGGCCATGGAGGATCCACTACACTCCAGCCTGG T C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs998661440 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16582 18349 RMVar_ID_18349 Human_SNP_ID_176114892 A-to-I Human chr4 - 21221681 21221681 21221681 CCAGAGTGGAGTTGCCAAAATGATGCTCTGATATGGTTAGGCTTTGTGTCCCCACCCGAATATCA CCAGAGTGGAGTTGCCAAAATGATGCTCTGATGTGGTTAGGCTTTGTGTCCCCACCCGAATATCA T C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1353704775 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16582 18350 RMVar_ID_18350 Human_SNP_ID_176117229 A-to-I Human chr4 - 21230792 21230792 21230792 TATGTTCATTGCAGCACTAGTCACAATAGCAAAGACATGGAATCAAGCCAAATGTCCATAGATGA TATGTTCATTGCAGCACTAGTCACAATAGCAAGGACATGGAATCAAGCCAAATGTCCATAGATGA T C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1032570871 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16582 18351 RMVar_ID_18351 Human_SNP_ID_176119116 A-to-I Human chr4 - 21236090 21236090 21236090 GGATTTTACCATGTTGCCTAGGCTGGTCTCCAACTCCTGAACTCAAGCGATCTGCCTGCCTCAGC GGATTTTACCATGTTGCCTAGGCTGGTCTCCAGCTCCTGAACTCAAGCGATCTGCCTGCCTCAGC T C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1177180992 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16582 18352 RMVar_ID_18352 Human_SNP_ID_176125035 A-to-I Human chr4 - 21256333 21256333 21256333 CAAGCCATCATCCCGGAATGTGGGCCTCCCCAAATGCTGATATTACAGGCATGAGCCACTTTTCT CAAGCCATCATCCCGGAATGTGGGCCTCCCCAGATGCTGATATTACAGGCATGAGCCACTTTTCT T C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1205732088 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16582 18353 RMVar_ID_18353 Human_SNP_ID_176127298 A-to-I Human chr4 - 21264915 21264915 21264915 GTTTTATTTTTAGTAGAGATGGGAGTTTCACCATGTTGGCCAGGCTGGTCTCGAACACCTGACCT GTTTTATTTTTAGTAGAGATGGGAGTTTCACCGTGTTGGCCAGGCTGGTCTCGAACACCTGACCT T C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs563219608 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16582 18354 RMVar_ID_18354 Human_SNP_ID_176130305 A-to-I Human chr4 - 21276428 21276428 21276428 GGCTGAGGCAGGTGGATCACTACTTGAAGTCAAGCGTTCGAGACCAGCCTGGCCAACATGGTGAA GGCTGAGGCAGGTGGATCACTACTTGAAGTCAGGCGTTCGAGACCAGCCTGGCCAACATGGTGAA T C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1043577058 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16582 18355 RMVar_ID_18355 Human_SNP_ID_176156469 A-to-I Human chr4 - 21375788 21375788 21375788 CTGAGGCGGGCCAATCACGAGGTCAGGAGATCAAGACCATCCTGGTAACACGGTGAAACCCCGCC CTGAGGCGGGCCAATCACGAGGTCAGGAGATCGAGACCATCCTGGTAACACGGTGAAACCCCGCC T C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1025968363 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16582 18356 RMVar_ID_18356 Human_SNP_ID_176156470 A-to-I Human chr4 - 21375788 21375788 21375788 CTGAGGCGGGCCAATCACGAGGTCAGGAGATCAAGACCATCCTGGTAACACGGTGAAACCCCGCC CTGAGGCGGGCCAATCACGAGGTCAGGAGATCCAGACCATCCTGGTAACACGGTGAAACCCCGCC T G KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1025968363 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16582 18357 RMVar_ID_18357 Human_SNP_ID_176160009 A-to-I Human chr4 - 21389110 21389110 21389110 ATGGTGGCACACACCTATAGTCCCAGCTTCTAAGGAAGTTGCGGTGGGAGGATCACCTGAGCCCA ATGGTGGCACACACCTATAGTCCCAGCTTCTAGGGAAGTTGCGGTGGGAGGATCACCTGAGCCCA T C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1254297467 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16582 18358 RMVar_ID_18358 Human_SNP_ID_176165686 A-to-I Human chr4 - 21411729 21411729 21411729 GGCTCAAGTGATCCTCCCACTTTGGCCCCCCAAGTAGCTAAGACCACAGGCACATTCCTCCATAT GGCTCAAGTGATCCTCCCACTTTGGCCCCCCAGGTAGCTAAGACCACAGGCACATTCCTCCATAT T C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs909259386 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16582 18359 RMVar_ID_18359 Human_SNP_ID_176166627 A-to-I Human chr4 - 21415642 21415642 21415642 GCTGGAGTGCAATGGCACACTCTCAGCTCACTACAACCTCTGTCTCCCGGATTCAAGTGATTCTC GCTGGAGTGCAATGGCACACTCTCAGCTCACTGCAACCTCTGTCTCCCGGATTCAAGTGATTCTC T C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,frontal_cortex;ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs923636822 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16582 18360 RMVar_ID_18360 Human_SNP_ID_176168791 A-to-I Human chr4 - 21424359 21424359 21424359 ACCATGTTGGTCAGGCTGGTCTCGAACTCCTGACCTCGTGATCGTCCCACCTTGGCCTCCCAAAT ACCATGTTGGTCAGGCTGGTCTCGAACTCCTGGCCTCGTGATCGTCCCACCTTGGCCTCCCAAAT T C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,frontal_cortex;ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1193118124 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16582 18361 RMVar_ID_18361 Human_SNP_ID_176178196 A-to-I Human chr4 - 21460480 21460480 21460480 TCCATATCATGATCTTCCCAACATCCAGAACTATGAGAAATAAATTCCTGTTGTTTAAGCCATGC TCCATATCATGATCTTCCCAACATCCAGAACTGTGAGAAATAAATTCCTGTTGTTTAAGCCATGC T C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1160783378 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9155746 RMVar_hsa_circ_16582 18362 RMVar_ID_18362 Human_SNP_ID_176178700 A-to-I Human chr4 - 21462432 21462429 21462433 CAGGTCTTTCCCATTCTTCTCTGGTGATAGTGAGTAAGTCTCATGAGATCTGATGGTTATTATAA CAGGTCTTTCCCATTCTTCTCTGGTGATAGT____AAGTCTCATGAGATCTGATGGTTATTATAA TACTC T KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs562758174 Functional Loss DEL dbSNP153 32..35 33 - - - RMVar_hsa_circ_16582 18363 RMVar_ID_18363 Human_SNP_ID_176178712 A-to-I Human chr4 - 21462491 21462491 21462491 ATCTTGAATTCCCGTGTGTTGTGGGAGGGACCAGGTGGGAGGTAATTGAATCATGGGGGCAGGTC ATCTTGAATTCCCGTGTGTTGTGGGAGGGACCGGGTGGGAGGTAATTGAATCATGGGGGCAGGTC T C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs947858701 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16582 18364 RMVar_ID_18364 Human_SNP_ID_176179292 A-to-I Human chr4 - 21464765 21464765 21464765 CTTTGGTATGGAACATTGTGTAAATGTCTGTCAGGTCTATCTGGTGTATAGCGTTGCTCAAGTCC CTTTGGTATGGAACATTGTGTAAATGTCTGTCGGGTCTATCTGGTGTATAGCGTTGCTCAAGTCC T C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1465416650 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9155766 RMVar_hsa_circ_16582 18365 RMVar_ID_18365 Human_SNP_ID_176186240 A-to-I Human chr4 - 21492292 21492292 21492292 ATCACTTGAGTCCCGGAGTTCAAGACTGTAGTAAGCTATTATCATGCCACTGCACTCCAACTTGG ATCACTTGAGTCCCGGAGTTCAAGACTGTAGTTAGCTATTATCATGCCACTGCACTCCAACTTGG T A KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1189281251 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16582 18366 RMVar_ID_18366 Human_SNP_ID_176190012 A-to-I Human chr4 - 21506900 21506898 21506901 GTAGTCCCATCTACTTGGGAGGCTGAGACAGAAGGATTGCTTTGGCCCAGGAGTTTGAGGCTGCA GTAGTCCCATCTACTTGGGAGGCTGAGACAG___GATTGCTTTGGCCCAGGAGTTTGAGGCTGCA CCTT C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1405518438 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_16582 18367 RMVar_ID_18367 Human_SNP_ID_176195979 A-to-I Human chr4 - 21528545 21528545 21528545 GTCCTGTCTCAACCTCCTGAGTAGCTGGGACTATAGGCGCCCGCCACCACACCCAGCTAATTTTT GTCCTGTCTCAACCTCCTGAGTAGCTGGGACTGTAGGCGCCCGCCACCACACCCAGCTAATTTTT T C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs543794119 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16582 18368 RMVar_ID_18368 Human_SNP_ID_176198309 A-to-I Human chr4 - 21536534 21536533 21536534 CCTCAAGCGATCTGCCTGCCTTGGCCTCCCAAAGTGCTGAGATTACAGGCTTGAGCCACCGTGCC CCTCAAGCGATCTGCCTGCCTTGGCCTCCCAA_GTGCTGAGATTACAGGCTTGAGCCACCGTGCC CT C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1331625090 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_16582 18369 RMVar_ID_18369 Human_SNP_ID_176199170 A-to-I Human chr4 - 21539915 21539915 21539915 GGAGTGCAATGGCACAATCTCAGCTCACTGCAACTGCCACCTCCCGGTTCAAGCGATTCTCCTGC GGAGTGCAATGGCACAATCTCAGCTCACTGCATCTGCCACCTCCCGGTTCAAGCGATTCTCCTGC T A KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs563854303 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16582 18370 RMVar_ID_18370 Human_SNP_ID_176199171 A-to-I Human chr4 - 21539915 21539915 21539915 GGAGTGCAATGGCACAATCTCAGCTCACTGCAACTGCCACCTCCCGGTTCAAGCGATTCTCCTGC GGAGTGCAATGGCACAATCTCAGCTCACTGCAGCTGCCACCTCCCGGTTCAAGCGATTCTCCTGC T C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs563854303 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16582 18371 RMVar_ID_18371 Human_SNP_ID_176207194 A-to-I Human chr4 - 21572846 21572846 21572846 GAGGCCAGTGGATCACCTGAGGTCAGGAGTTAAAGAGCAGTCTGGCCAACATGGAGAAACCCCAT GAGGCCAGTGGATCACCTGAGGTCAGGAGTTAGAGAGCAGTCTGGCCAACATGGAGAAACCCCAT T C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1346889091 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16582 18372 RMVar_ID_18372 Human_SNP_ID_176207195 A-to-I Human chr4 - 21572846 21572846 21572846 GAGGCCAGTGGATCACCTGAGGTCAGGAGTTAAAGAGCAGTCTGGCCAACATGGAGAAACCCCAT GAGGCCAGTGGATCACCTGAGGTCAGGAGTTACAGAGCAGTCTGGCCAACATGGAGAAACCCCAT T G KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1346889091 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16582 18373 RMVar_ID_18373 Human_SNP_ID_176207196 A-to-I Human chr4 - 21572847 21572847 21572847 AGAGGCCAGTGGATCACCTGAGGTCAGGAGTTAAAGAGCAGTCTGGCCAACATGGAGAAACCCCA AGAGGCCAGTGGATCACCTGAGGTCAGGAGTTCAAGAGCAGTCTGGCCAACATGGAGAAACCCCA T G KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1208409399 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16582 18374 RMVar_ID_18374 Human_SNP_ID_176207210 A-to-I Human chr4 - 21572916 21572916 21572916 AAAGGCAAGAAAAGAAGGATGAGACCAGGTGGAATGGCTCACGCCTATAATCCCAGCACTTTGGG AAAGGCAAGAAAAGAAGGATGAGACCAGGTGGCATGGCTCACGCCTATAATCCCAGCACTTTGGG T G KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs982585247 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16582 18375 RMVar_ID_18375 Human_SNP_ID_176208450 A-to-I Human chr4 - 21578247 21578247 21578247 CTCACTGCAACGTCCGCCTCCCGGGTTCAGGCAATTCTCTGCCTCAGCCTCCTAAGTAGCTGGGA CTCACTGCAACGTCCGCCTCCCGGGTTCAGGCTATTCTCTGCCTCAGCCTCCTAAGTAGCTGGGA T A KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs531473537 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16582 18376 RMVar_ID_18376 Human_SNP_ID_176216468 A-to-I Human chr4 - 21610691 21610691 21610691 TTACCCAGTCTCGGGTTTTTCTTTGTAGCAGTATGAAAATGTATGAATAAACTCATTTACACAAA TTACCCAGTCTCGGGTTTTTCTTTGTAGCAGTGTGAAAATGTATGAATAAACTCATTTACACAAA T C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1158857902 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16582 18377 RMVar_ID_18377 Human_SNP_ID_176216922 A-to-I Human chr4 - 21612415 21612415 21612415 TTGAGATGGATTCTTGCTATGTTACCCAGACTAGTTTCAAACTTCTGGGCTCAAGTGATTTCCAA TTGAGATGGATTCTTGCTATGTTACCCAGACTGGTTTCAAACTTCTGGGCTCAAGTGATTTCCAA T C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1459227405 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16582 18378 RMVar_ID_18378 Human_SNP_ID_176217318 A-to-I Human chr4 - 21614119 21614119 21614119 TTTTTTTGAGATAGAGTCTCGCTTTCTCACCCAGGCTGGAGTGCAGCCCCACCATCTCGGCTCAC TTTTTTTGAGATAGAGTCTCGCTTTCTCACCCGGGCTGGAGTGCAGCCCCACCATCTCGGCTCAC T C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs551141755 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16582 18379 RMVar_ID_18379 Human_SNP_ID_176218884 A-to-I Human chr4 - 21620390 21620390 21620390 TCAAGAGATCCTTCCATCTCAGCCTCCTGAGTAGCTGGGACTACAGACATGTGCCATCATGCCCA TCAAGAGATCCTTCCATCTCAGCCTCCTGAGTTGCTGGGACTACAGACATGTGCCATCATGCCCA T A KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs977280738 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16582 18380 RMVar_ID_18380 Human_SNP_ID_176221053 A-to-I Human chr4 - 21629953 21629953 21629953 TCAGCTAGTAGAGAGGATTAGGTGGGAGGATCATTTGAGACCAGGAGGTTAAGCCTACAGTGAGC TCAGCTAGTAGAGAGGATTAGGTGGGAGGATCGTTTGAGACCAGGAGGTTAAGCCTACAGTGAGC T C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1262181876 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16582 18381 RMVar_ID_18381 Human_SNP_ID_176221156 A-to-I Human chr4 - 21630282 21630282 21630282 TTTTGTATTTTTAGTAGAGATGGGGTTTTACCATGTTGGGCAGGATGGTCTCAATCTCTTGACCT TTTTGTATTTTTAGTAGAGATGGGGTTTTACCTTGTTGGGCAGGATGGTCTCAATCTCTTGACCT T A KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1018725718 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16582 18382 RMVar_ID_18382 Human_SNP_ID_176225646 A-to-I Human chr4 - 21648038 21648038 21648038 AAACCCCATCTCCACTAAAAATACAAAAAATTAGCTGGGCGTGGTGGCGAGCGTCTGTAGTCCCA AAACCCCATCTCCACTAAAAATACAAAAAATTCGCTGGGCGTGGTGGCGAGCGTCTGTAGTCCCA T G KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1401722161 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16582 18383 RMVar_ID_18383 Human_SNP_ID_176236084 A-to-I Human chr4 - 21690364 21690364 21690364 GCCACCACCTCCAACACTGGGATCACATTTCAACATGAGATTTGGAGGGGACAAAACATCCAAAC GCCACCACCTCCAACACTGGGATCACATTTCACCATGAGATTTGGAGGGGACAAAACATCCAAAC T G KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs569853608 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16582,RMVar_hsa_circ_225086 18384 RMVar_ID_18384 Human_SNP_ID_176236165 A-to-I Human chr4 - 21690694 21690694 21690694 TGGCTGTGTTACTCTGTTTTGCATTGCTGTAAAGGAATACCTGAGGCTGGGTAATTTATAAAGAA TGGCTGTGTTACTCTGTTTTGCATTGCTGTAAGGGAATACCTGAGGCTGGGTAATTTATAAAGAA T C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1360838595 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16582,RMVar_hsa_circ_225086 18385 RMVar_ID_18385 Human_SNP_ID_176236301 A-to-I Human chr4 - 21691288 21691288 21691288 GAATATAGCCTACCCACAGAGGCCTGTTAGGAAGAAAGCTCAGGGAAGAAAAAAATGCTGGTCTC GAATATAGCCTACCCACAGAGGCCTGTTAGGAGGAAAGCTCAGGGAAGAAAAAAATGCTGGTCTC T C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs908414111 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16582,RMVar_hsa_circ_225086 18386 RMVar_ID_18386 Human_SNP_ID_176243930 A-to-I Human chr4 - 21719924 21719924 21719924 AGCTTCACTCTTGTTGCCCATGCTGGAGCACAATGGCACAATCTCAGCTCGCTGTAACCTCTGCC AGCTTCACTCTTGTTGCCCATGCTGGAGCACAGTGGCACAATCTCAGCTCGCTGTAACCTCTGCC T C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs968423375 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16582,RMVar_hsa_circ_225086 18387 RMVar_ID_18387 Human_SNP_ID_176251729 A-to-I Human chr4 - 21752278 21752278 21752278 TAAGTTTCCTGAGGCGCCCCCCTCAGCCATGCAGAAATGTGAGTCAATTAAACCTTTTTCTTTTA TAAGTTTCCTGAGGCGCCCCCCTCAGCCATGCGGAAATGTGAGTCAATTAAACCTTTTTCTTTTA T C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1462329666 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16582,RMVar_hsa_circ_225086 18388 RMVar_ID_18388 Human_SNP_ID_176254808 A-to-I Human chr4 - 21763034 21763034 21763034 TTAGGCAAACTGTGCATATGTCCATTCAATCTAGAAGCGGTTATTGAGCATTCGCTGTGTACCAA TTAGGCAAACTGTGCATATGTCCATTCAATCTGGAAGCGGTTATTGAGCATTCGCTGTGTACCAA T C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs904279769 Functional Loss SNV dbSNP153 33..33 33 - - - 18389 RMVar_ID_18389 Human_SNP_ID_176255493 A-to-I Human chr4 - 21765703 21765703 21765703 CCAGCTACTAGGGAGGCTGAGATGGGAGGATCACATGAGGTCAGGAGGTCAAGACCAGTCTGAGC CCAGCTACTAGGGAGGCTGAGATGGGAGGATCGCATGAGGTCAGGAGGTCAAGACCAGTCTGAGC T C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs754386888 Functional Loss SNV dbSNP153 33..33 33 - - - 18390 RMVar_ID_18390 Human_SNP_ID_176258599 A-to-I Human chr4 - 21777199 21777199 21777199 GGTTTAATTGACTCACAATTCTGCATGGCTGGAGAAGCCTCAGGAAACTTACAATCATGGAAGAT GGTTTAATTGACTCACAATTCTGCATGGCTGGGGAAGCCTCAGGAAACTTACAATCATGGAAGAT T C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1337472924 Functional Loss SNV dbSNP153 33..33 33 - - - 18391 RMVar_ID_18391 Human_SNP_ID_176258955 A-to-I Human chr4 - 21778462 21778460 21778462 CACTTTGGGAGGCCGAGGTGGGAGTTCAACCCAAGAGTTCAAGACCAGCCTGGGTAACATGATGC CACTTTGGGAGGCCGAGGTGGGAGTTCAACCC__GAGTTCAAGACCAGCCTGGGTAACATGATGC CTT C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs555374580 Functional Loss DEL dbSNP153 33..34 33 - - - 18392 RMVar_ID_18392 Human_SNP_ID_176258960 A-to-I Human chr4 - 21778501 21778501 21778501 ATATACACCCAGCACAGTGGCTCACACCTGTAATCTCAGCACTTTGGGAGGCCGAGGTGGGAGTT ATATACACCCAGCACAGTGGCTCACACCTGTATTCTCAGCACTTTGGGAGGCCGAGGTGGGAGTT T A KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs986476964 Functional Loss SNV dbSNP153 33..33 33 - - - 18393 RMVar_ID_18393 Human_SNP_ID_176259292 A-to-I Human chr4 - 21779831 21779831 21779831 GAACTCTTGGGCTCAAGTGATCCTCCTGCTTCAGCCTCCCGACAGGCTGGGACTACAGGAGGAAG GAACTCTTGGGCTCAAGTGATCCTCCTGCTTCGGCCTCCCGACAGGCTGGGACTACAGGAGGAAG T C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1485903075 Functional Loss SNV dbSNP153 33..33 33 - - - 18394 RMVar_ID_18394 Human_SNP_ID_176260630 A-to-I Human chr4 - 21785334 21785334 21785334 AGCCTCCCTTGGCCTCACAAAGTGCTGGGATTACAGGTGTGAACCACTGTGGCCAGCCAAGTTTT AGCCTCCCTTGGCCTCACAAAGTGCTGGGATTGCAGGTGTGAACCACTGTGGCCAGCCAAGTTTT T C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs562743946 Functional Loss SNV dbSNP153 33..33 33 - - - 18395 RMVar_ID_18395 Human_SNP_ID_176261592 A-to-I Human chr4 - 21788949 21788949 21788949 TCTGCCTCAGCCTCCCAAGTAGTTGAGACTACAGACGCGCGCCGCCACGCCTGGCTAATTGTTGT TCTGCCTCAGCCTCCCAAGTAGTTGAGACTACGGACGCGCGCCGCCACGCCTGGCTAATTGTTGT T C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1441020829 Functional Loss SNV dbSNP153 33..33 33 - - - 18396 RMVar_ID_18396 Human_SNP_ID_176264283 A-to-I Human chr4 - 21798633 21798633 21798633 AGCTTAACAGCTTATTTTTTTCTCATTCTCTTAATCTATTGGAGAATAGCTTAAAAGAGTGGCTC AGCTTAACAGCTTATTTTTTTCTCATTCTCTTCATCTATTGGAGAATAGCTTAAAAGAGTGGCTC T G KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1283748381 Functional Loss SNV dbSNP153 33..33 33 - - - 18397 RMVar_ID_18397 Human_SNP_ID_176269721 A-to-I Human chr4 - 21820728 21820728 21820728 TCATTGAAGCTAACTGAAATGTCAGTGAACTTAGAGAAATGTAATTATGATGCAAATGTGAAATT TCATTGAAGCTAACTGAAATGTCAGTGAACTTGGAGAAATGTAATTATGATGCAAATGTGAAATT T C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs893981440 Functional Loss SNV dbSNP153 33..33 33 - - - 18398 RMVar_ID_18398 Human_SNP_ID_176272424 A-to-I Human chr4 - 21832142 21832142 21832142 ATGCTTCATTTTTGCATCTATGAAAGAATTATATGATTTTTGTCTTTCAGGTTGTTAATGTGGTA ATGCTTCATTTTTGCATCTATGAAAGAATTATGTGATTTTTGTCTTTCAGGTTGTTAATGTGGTA T C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs760932623 Functional Loss SNV dbSNP153 33..33 33 - - - 18399 RMVar_ID_18399 Human_SNP_ID_176279302 A-to-I Human chr4 - 21860003 21860003 21860003 AGCGTCTCTCTCAGTTGTCCAGCCTGGAGTGCAGTGGCACCATCACAGCTCATTACAGCCTAGAC AGCGTCTCTCTCAGTTGTCCAGCCTGGAGTGCGGTGGCACCATCACAGCTCATTACAGCCTAGAC T C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1469059621 Functional Loss SNV dbSNP153 33..33 33 - - - 18400 RMVar_ID_18400 Human_SNP_ID_176284341 A-to-I Human chr4 - 21879805 21879803 21879805 TCAATTACCTCCCACCGGGTCCCTTCCATGACATGTGGGGATTATGGGAACTATAAGATGAGATT TCAATTACCTCCCACCGGGTCCCTTCCATGAC__GTGGGGATTATGGGAACTATAAGATGAGATT CAT C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1422266097 Functional Loss DEL dbSNP153 33..34 33 - - - 18401 RMVar_ID_18401 Human_SNP_ID_176288676 A-to-I Human chr4 - 21898270 21898270 21898270 AGCTGGCATCTTGCTAGGTCATGTGCATCCCAAGACCACTGACTCCAAGCCCAGCACAGCACCAG AGCTGGCATCTTGCTAGGTCATGTGCATCCCATGACCACTGACTCCAAGCCCAGCACAGCACCAG T A KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs932147970 Functional Loss SNV dbSNP153 33..33 33 - - - 18402 RMVar_ID_18402 Human_SNP_ID_176291038 A-to-I Human chr4 - 21908685 21908685 21908685 AGCTCTAAAATCCTTCCTAAACCTTATAAGGAACTGAATGATCCCTAACTTCCTCTCCAATCTCA AGCTCTAAAATCCTTCCTAAACCTTATAAGGAGCTGAATGATCCCTAACTTCCTCTCCAATCTCA T C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs985101022 Functional Loss SNV dbSNP153 33..33 33 - - - 18403 RMVar_ID_18403 Human_SNP_ID_176291048 A-to-I Human chr4 - 21908729 21908729 21908729 AAGACACTGTAGAAATAAAATGATTTCTGATTAAATTGAGAATAAGCTCTAAAATCCTTCCTAAA AAGACACTGTAGAAATAAAATGATTTCTGATTGAATTGAGAATAAGCTCTAAAATCCTTCCTAAA T C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1186995827 Functional Loss SNV dbSNP153 33..33 33 - - - 18404 RMVar_ID_18404 Human_SNP_ID_176293207 A-to-I Human chr4 - 21917272 21917272 21917272 AAATTAGCTGGGTGTGGCGGTGTATGCCTGTAATCCCAGCTATTCAGGAGGCTGAGGCAGGAGAA AAATTAGCTGGGTGTGGCGGTGTATGCCTGTATTCCCAGCTATTCAGGAGGCTGAGGCAGGAGAA T A KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1465457513 Functional Loss SNV dbSNP153 33..33 33 - - - 18405 RMVar_ID_18405 Human_SNP_ID_176294687 A-to-I Human chr4 - 21923434 21923434 21923434 TGGGATTACAGGCATGTACCACCACTCCGGCTAATTTTTGTATTTTTAATAGAGACAGGGTTTTA TGGGATTACAGGCATGTACCACCACTCCGGCTGATTTTTGTATTTTTAATAGAGACAGGGTTTTA T C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1027982434 Functional Loss SNV dbSNP153 33..33 33 - - - 18406 RMVar_ID_18406 Human_SNP_ID_176294711 A-to-I Human chr4 - 21923542 21923542 21923542 GTGTCTCACTCTGTCACCTAGGCTGGAGTGCAATGGCATGATCTTGGCTCACTTCAATCTCTACC GTGTCTCACTCTGTCACCTAGGCTGGAGTGCAGTGGCATGATCTTGGCTCACTTCAATCTCTACC T C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs968416117 Functional Loss SNV dbSNP153 33..33 33 - - - 18407 RMVar_ID_18407 Human_SNP_ID_176294987 A-to-I Human chr4 - 21924523 21924523 21924523 TAGAAATATATTGTCCAGGCGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGAC TAGAAATATATTGTCCAGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGAC T C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1240352022 Functional Loss SNV dbSNP153 33..33 33 - - - 18408 RMVar_ID_18408 Human_SNP_ID_176421025 A-to-I Human chr4 - 22412646 22412646 22412646 GTTTTAATGCCAGTCTAGTGTTGTTTTCTGTTATTTGCCGTTGTTAACACTAATTACAGGTTGAG GTTTTAATGCCAGTCTAGTGTTGTTTTCTGTTGTTTGCCGTTGTTAACACTAATTACAGGTTGAG T C ADGRA3 Ensembl:ENSG00000152990 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1197626231 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_272499,RMVar_hsa_circ_295025,RMVar_hsa_circ_361623,RMVar_hsa_circ_370911,RMVar_hsa_circ_67887,RMVar_hsa_circ_35221,RMVar_hsa_circ_57551,RMVar_hsa_circ_225102,RMVar_hsa_circ_225103,RMVar_hsa_circ_225101,RMVar_hsa_circ_59896,RMVar_hsa_circ_31520,RMVar_hsa_circ_41150,RMVar_hsa_circ_65578,RMVar_hsa_circ_315724,RMVar_hsa_circ_345381,RMVar_hsa_circ_356563,RMVar_hsa_circ_335679,RMVar_hsa_circ_225110,RMVar_hsa_circ_64836,RMVar_hsa_circ_225109 18409 RMVar_ID_18409 Human_SNP_ID_176425304 A-to-I Human chr4 - 22429035 22429025 22429036 AGACACATCATCTCTCCTGAAGAATTATGATTATTACATGATCTGAGAACTCCTGCCATGCCTTA AGACACATCATCTCTCCTGAAGAATTATGAT___________CTGAGAACTCCTGCCATGCCTTA GATCATGTAATA G ADGRA3 Ensembl:ENSG00000152990 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs940011970 Functional Loss DEL dbSNP153 32..42 33 - - - Human_RBP_ID_15126781 RMVar_hsa_circ_295025,RMVar_hsa_circ_361623,RMVar_hsa_circ_370911,RMVar_hsa_circ_35221,RMVar_hsa_circ_225103,RMVar_hsa_circ_41150,RMVar_hsa_circ_65578,RMVar_hsa_circ_315724,RMVar_hsa_circ_345381,RMVar_hsa_circ_356563,RMVar_hsa_circ_225110,RMVar_hsa_circ_225109,RMVar_hsa_circ_24804,RMVar_hsa_circ_318281,RMVar_hsa_circ_353261,RMVar_hsa_circ_311767,RMVar_hsa_circ_11106,RMVar_hsa_circ_225112,RMVar_hsa_circ_225113,RMVar_hsa_circ_112471,RMVar_hsa_circ_354923,RMVar_hsa_circ_357149,RMVar_hsa_circ_225114,RMVar_hsa_circ_44613,RMVar_hsa_circ_326188 18410 RMVar_ID_18410 Human_SNP_ID_176425309 A-to-I Human chr4 - 22429058 22429058 22429058 GATCAAGCATGAGACCTGATGGTAGACACATCATCTCTCCTGAAGAATTATGATTATTACATGAT GATCAAGCATGAGACCTGATGGTAGACACATCGTCTCTCCTGAAGAATTATGATTATTACATGAT T C ADGRA3 Ensembl:ENSG00000152990 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs747507022 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_295025,RMVar_hsa_circ_361623,RMVar_hsa_circ_370911,RMVar_hsa_circ_35221,RMVar_hsa_circ_225103,RMVar_hsa_circ_41150,RMVar_hsa_circ_65578,RMVar_hsa_circ_315724,RMVar_hsa_circ_345381,RMVar_hsa_circ_356563,RMVar_hsa_circ_225110,RMVar_hsa_circ_225109,RMVar_hsa_circ_24804,RMVar_hsa_circ_318281,RMVar_hsa_circ_353261,RMVar_hsa_circ_311767,RMVar_hsa_circ_11106,RMVar_hsa_circ_225112,RMVar_hsa_circ_225113,RMVar_hsa_circ_112471,RMVar_hsa_circ_354923,RMVar_hsa_circ_357149,RMVar_hsa_circ_225114,RMVar_hsa_circ_44613,RMVar_hsa_circ_326188 18411 RMVar_ID_18411 Human_SNP_ID_176425310 A-to-I Human chr4 - 22429061 22429061 22429061 GAGGATCAAGCATGAGACCTGATGGTAGACACATCATCTCTCCTGAAGAATTATGATTATTACAT GAGGATCAAGCATGAGACCTGATGGTAGACACGTCATCTCTCCTGAAGAATTATGATTATTACAT T C ADGRA3 Ensembl:ENSG00000152990 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs942076747 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_295025,RMVar_hsa_circ_361623,RMVar_hsa_circ_370911,RMVar_hsa_circ_35221,RMVar_hsa_circ_225103,RMVar_hsa_circ_41150,RMVar_hsa_circ_65578,RMVar_hsa_circ_315724,RMVar_hsa_circ_345381,RMVar_hsa_circ_356563,RMVar_hsa_circ_225110,RMVar_hsa_circ_225109,RMVar_hsa_circ_24804,RMVar_hsa_circ_318281,RMVar_hsa_circ_353261,RMVar_hsa_circ_311767,RMVar_hsa_circ_11106,RMVar_hsa_circ_225112,RMVar_hsa_circ_225113,RMVar_hsa_circ_112471,RMVar_hsa_circ_354923,RMVar_hsa_circ_357149,RMVar_hsa_circ_225114,RMVar_hsa_circ_44613,RMVar_hsa_circ_326188 18412 RMVar_ID_18412 Human_SNP_ID_176953093 A-to-I Human chr4 - 24530576 24530576 24530576 TTTTTATTCTATTTCTTTATTTTCTTTTTTGAAATGGAGCCTCTCGGTCTGTCGCCCAGGCTGGA TTTTTATTCTATTTCTTTATTTTCTTTTTTGAGATGGAGCCTCTCGGTCTGTCGCCCAGGCTGGA T C DHX15 Ensembl:ENSG00000109606 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs570369792 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15128271,Human_RBP_ID_21037222,Human_RBP_ID_25803948 RMVar_hsa_circ_36526,RMVar_hsa_circ_73969,RMVar_hsa_circ_44058 18413 RMVar_ID_18413 Human_SNP_ID_176962641 A-to-I Human chr4 - 24566824 24566824 24566824 AGATGTTGGATTTATTTATTTATTTTTGAGATAGAGTCTCATCTCATCTGTCACTCAGGCTGGAG AGATGTTGGATTTATTTATTTATTTTTGAGATGGAGTCTCATCTCATCTGTCACTCAGGCTGGAG T C DHX15 Ensembl:ENSG00000109606 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1462057356 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8589859 RMVar_hsa_circ_7805,RMVar_hsa_circ_65157,RMVar_hsa_circ_73969,RMVar_hsa_circ_28349,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 18414 RMVar_ID_18414 Human_SNP_ID_177097585 A-to-I Human chr4 - 25120962 25120962 25120962 TGTGGTTCTGTGTCTTTAACCACCTCATAATAAGAACTGTTATTGAGGACTGGGCTACAGAATGT TGTGGTTCTGTGTCTTTAACCACCTCATAATAGGAACTGTTATTGAGGACTGGGCTACAGAATGT T C SEPSECS Ensembl:ENSG00000109618 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904452696 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9159139 18415 RMVar_ID_18415 Human_SNP_ID_177106600 A-to-I Human chr4 - 25159650 25159650 25159650 CGCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCCGCCACCACACCCGGTTAATGTTT CGCCTGCCTCAGCCTCCCGAGTAGCTGGGACTGCAGGCGCCCGCCACCACACCCGGTTAATGTTT T C SEPSECS Ensembl:ENSG00000109618 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1424916975 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_551013 18416 RMVar_ID_18416 Human_SNP_ID_177106663 A-to-I Human chr4 - 25159766 25159766 25159766 AAAAGTTTTGTTGTGTTTTGTTTTTTTGAAACAGAGTCTCGCTCTTTCGCCCAGGCTGGAATGCA AAAAGTTTTGTTGTGTTTTGTTTTTTTGAAACGGAGTCTCGCTCTTTCGCCCAGGCTGGAATGCA T C SEPSECS Ensembl:ENSG00000109618 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1311952603 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2844064,Human_RBP_ID_3737134,Human_RBP_ID_8589932,Human_RBP_ID_8881958 18417 RMVar_ID_18417 Human_SNP_ID_177114925 A-to-I Human chr4 + 25195524 25195523 25195525 ATATCTTACTACGACTTCTAACTCCTGGGCTCAAGTGATCCTCCTGCCTTGGCCTCCCAAATCTT ATATCTTACTACGACTTCTAACTCCTGGGCTC__GTGATCCTCCTGCCTTGGCCTCCCAAATCTT CAA C PI4K2B,SEPSECS-AS1 Ensembl:ENSG00000038210,Ensembl:ENSG00000281501 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1425246307 Functional Loss DEL dbSNP153 33..34 33 - - - 18418 RMVar_ID_18418 Human_SNP_ID_177115247 A-to-I Human chr4 + 25196924 25196924 25196924 GCTGGAGTGCGGTGGCACTATCTCGGCTCACTACAACCTTGACCTCCTAGGCTCAAGCAATCCTC GCTGGAGTGCGGTGGCACTATCTCGGCTCACTGCAACCTTGACCTCCTAGGCTCAAGCAATCCTC A G PI4K2B,SEPSECS-AS1 Ensembl:ENSG00000038210,Ensembl:ENSG00000281501 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1371524165 Functional Loss SNV dbSNP153 33..33 33 - - - 18419 RMVar_ID_18419 Human_SNP_ID_177132389 A-to-I Human chr4 + 25267434 25267434 25267434 AGTGAGAGCCAGGCGCTGAGGCGCACTCCTGTAGTCCTAGCTACTTGGGAGGCTGAGGCGAGAGA AGTGAGAGCCAGGCGCTGAGGCGCACTCCTGTCGTCCTAGCTACTTGGGAGGCTGAGGCGAGAGA A C PI4K2B Ensembl:ENSG00000038210 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs975869216 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_317113,RMVar_hsa_circ_7442,RMVar_hsa_circ_225139,RMVar_hsa_circ_313284,RMVar_hsa_circ_225143,RMVar_hsa_circ_64217,RMVar_hsa_circ_320695,RMVar_hsa_circ_225144 18420 RMVar_ID_18420 Human_SNP_ID_177132404 A-to-I Human chr4 + 25267504 25267504 25267504 TTGAGCCCAGGAGATTGAGGCTATAGCGAACTATGATTGTGCCACTGCACCCTAGCCTGAGTGAC TTGAGCCCAGGAGATTGAGGCTATAGCGAACTGTGATTGTGCCACTGCACCCTAGCCTGAGTGAC A G PI4K2B Ensembl:ENSG00000038210 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1047641271 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15130907,Human_RBP_ID_24051461 RMVar_hsa_circ_317113,RMVar_hsa_circ_7442,RMVar_hsa_circ_225139,RMVar_hsa_circ_313284,RMVar_hsa_circ_225143,RMVar_hsa_circ_64217,RMVar_hsa_circ_320695,RMVar_hsa_circ_225144 18421 RMVar_ID_18421 Human_SNP_ID_177132823 A-to-I Human chr4 + 25269387 25269387 25269387 GGCCGACTGCAGTGGCTCACGCCTGTAATCCCAGTGCTTTGGGAGGCCAAGGCGGGTGAATCACC GGCCGACTGCAGTGGCTCACGCCTGTAATCCCGGTGCTTTGGGAGGCCAAGGCGGGTGAATCACC A G PI4K2B Ensembl:ENSG00000038210 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs922732517 Functional Loss SNV dbSNP153 33..33 33 - - - 18422 RMVar_ID_18422 Human_SNP_ID_177133441 A-to-I Human chr4 + 25272022 25272022 25272022 AAAATTAGCCACGCATGGTGGCATGTGTTTGTAGTTCCAGCTGCCAGGAGCCTGAGGCAGGAGGA AAAATTAGCCACGCATGGTGGCATGTGTTTGTCGTTCCAGCTGCCAGGAGCCTGAGGCAGGAGGA A C PI4K2B Ensembl:ENSG00000038210 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs982660558 Functional Loss SNV dbSNP153 33..33 33 - - - 18423 RMVar_ID_18423 Human_SNP_ID_177135096 A-to-I Human chr4 + 25279411 25279410 25279411 TATTTTTAGTAGAGATGGAGTTTCACTATGTTAGCCAGGCTGGTCTTGAACTCCTGACCTCAAAT TATTTTTAGTAGAGATGGAGTTTCACTATGTT_GCCAGGCTGGTCTTGAACTCCTGACCTCAAAT TA T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1225765188 Functional Loss DEL dbSNP153 33..33 33 - - - 18424 RMVar_ID_18424 Human_SNP_ID_177135226 A-to-I Human chr4 + 25279930 25279930 25279930 AGATCACACCACTGCCTTCCAGCCTGGGTGACAGAGTAGATTCTGTCTCAAACAAACAAACAAAC AGATCACACCACTGCCTTCCAGCCTGGGTGACGGAGTAGATTCTGTCTCAAACAAACAAACAAAC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs957323833 Functional Loss SNV dbSNP153 33..33 33 - - - 18425 RMVar_ID_18425 Human_SNP_ID_177257759 A-to-I Human chr4 - 25761280 25761280 25761280 GTGGCTGTGGGCACCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCCA GTGGCTGTGGGCACCTGTAATCCCAGCTACTCTGGAGGCTGAGGCAGGAGAATCACTTGAACCCA T A SEL1L3 Ensembl:ENSG00000091490 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs920552452 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_225176,RMVar_hsa_circ_80062,RMVar_hsa_circ_225170,RMVar_hsa_circ_91944,RMVar_hsa_circ_107602,RMVar_hsa_circ_225171,RMVar_hsa_circ_291101,RMVar_hsa_circ_312066,RMVar_hsa_circ_353211,RMVar_hsa_circ_372739,RMVar_hsa_circ_300667,RMVar_hsa_circ_284601,RMVar_hsa_circ_29009,RMVar_hsa_circ_55676,RMVar_hsa_circ_61893,RMVar_hsa_circ_47895,RMVar_hsa_circ_225178,RMVar_hsa_circ_225180,RMVar_hsa_circ_25656,RMVar_hsa_circ_225179,RMVar_hsa_circ_225177,RMVar_hsa_circ_225172,RMVar_hsa_circ_225174,RMVar_hsa_circ_225175,RMVar_hsa_circ_225173,RMVar_hsa_circ_9054,RMVar_hsa_circ_83893,RMVar_hsa_circ_225182 18426 RMVar_ID_18426 Human_SNP_ID_177257760 A-to-I Human chr4 - 25761284 25761284 25761284 ATGCGTGGCTGTGGGCACCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAA ATGCGTGGCTGTGGGCACCTGTAATCCCAGCTGCTCAGGAGGCTGAGGCAGGAGAATCACTTGAA T C SEL1L3 Ensembl:ENSG00000091490 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1165993619 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_225176,RMVar_hsa_circ_80062,RMVar_hsa_circ_225170,RMVar_hsa_circ_91944,RMVar_hsa_circ_107602,RMVar_hsa_circ_225171,RMVar_hsa_circ_291101,RMVar_hsa_circ_312066,RMVar_hsa_circ_353211,RMVar_hsa_circ_372739,RMVar_hsa_circ_300667,RMVar_hsa_circ_284601,RMVar_hsa_circ_29009,RMVar_hsa_circ_55676,RMVar_hsa_circ_61893,RMVar_hsa_circ_47895,RMVar_hsa_circ_225178,RMVar_hsa_circ_225180,RMVar_hsa_circ_25656,RMVar_hsa_circ_225179,RMVar_hsa_circ_225177,RMVar_hsa_circ_225172,RMVar_hsa_circ_225174,RMVar_hsa_circ_225175,RMVar_hsa_circ_225173,RMVar_hsa_circ_9054,RMVar_hsa_circ_83893,RMVar_hsa_circ_225182 18427 RMVar_ID_18427 Human_SNP_ID_177258291 A-to-I Human chr4 - 25763745 25763745 25763745 GCCTTGGTCCCCCAGGCTCAAGCGATCCTCCTACCTCAGCCTCCTAAGTAGCTGGAAATACAAGT GCCTTGGTCCCCCAGGCTCAAGCGATCCTCCTCCCTCAGCCTCCTAAGTAGCTGGAAATACAAGT T G SEL1L3 Ensembl:ENSG00000091490 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs890450939 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_225176,RMVar_hsa_circ_80062,RMVar_hsa_circ_225170,RMVar_hsa_circ_91944,RMVar_hsa_circ_107602,RMVar_hsa_circ_225171,RMVar_hsa_circ_291101,RMVar_hsa_circ_312066,RMVar_hsa_circ_353211,RMVar_hsa_circ_372739,RMVar_hsa_circ_300667,RMVar_hsa_circ_284601,RMVar_hsa_circ_29009,RMVar_hsa_circ_55676,RMVar_hsa_circ_61893,RMVar_hsa_circ_47895,RMVar_hsa_circ_225178,RMVar_hsa_circ_225180,RMVar_hsa_circ_25656,RMVar_hsa_circ_225179,RMVar_hsa_circ_225177,RMVar_hsa_circ_225172,RMVar_hsa_circ_225174,RMVar_hsa_circ_225175,RMVar_hsa_circ_225173,RMVar_hsa_circ_9054,RMVar_hsa_circ_83893,RMVar_hsa_circ_225182 18428 RMVar_ID_18428 Human_SNP_ID_177262487 A-to-I Human chr4 - 25781408 25781408 25781408 GTCTTGAACTCCTGGCCTCAAGTGATCCGCCCACCTCCACCACCCAAAGTTCTGGGATTACAGGT GTCTTGAACTCCTGGCCTCAAGTGATCCGCCCGCCTCCACCACCCAAAGTTCTGGGATTACAGGT T C SEL1L3 Ensembl:ENSG00000091490 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054035449 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1064,RMVar_hsa_circ_225176,RMVar_hsa_circ_80062,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_47895,RMVar_hsa_circ_225172,RMVar_hsa_circ_225174,RMVar_hsa_circ_225175,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_344488,RMVar_hsa_circ_322405,RMVar_hsa_circ_290930,RMVar_hsa_circ_225184,RMVar_hsa_circ_225186,RMVar_hsa_circ_225187,RMVar_hsa_circ_225185,RMVar_hsa_circ_298383,RMVar_hsa_circ_322416,RMVar_hsa_circ_355128,RMVar_hsa_circ_225183,RMVar_hsa_circ_323607,RMVar_hsa_circ_320667,RMVar_hsa_circ_93851,RMVar_hsa_circ_282684,RMVar_hsa_circ_225194,RMVar_hsa_circ_225190,RMVar_hsa_circ_225192,RMVar_hsa_circ_225193,RMVar_hsa_circ_225191,RMVar_hsa_circ_354916,RMVar_hsa_circ_225189,RMVar_hsa_circ_345882 18429 RMVar_ID_18429 Human_SNP_ID_177265474 A-to-I Human chr4 - 25792823 25792823 25792823 CAAAACAAAACATTAAGAGCACCTTCCATATCAGACTGAGGGGATCTGAATTCTAACTGATCACT CAAAACAAAACATTAAGAGCACCTTCCATATCCGACTGAGGGGATCTGAATTCTAACTGATCACT T G SEL1L3 Ensembl:ENSG00000091490 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs570107750 Functional Loss SNV dbSNP153 33..33 33 - - - 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_23016,RMVar_hsa_circ_110703,RMVar_hsa_circ_225197,RMVar_hsa_circ_353273,RMVar_hsa_circ_23279,RMVar_hsa_circ_225198 18430 RMVar_ID_18430 Human_SNP_ID_177297581 A-to-I Human chr4 + 25925298 25925298 25925298 TTGCTCTTGCGCCCAGGCTCGAGTGCAGTGGCATGATCTTGGCTGACTACAACCTCTGACCCCCA TTGCTCTTGCGCCCAGGCTCGAGTGCAGTGGCGTGATCTTGGCTGACTACAACCTCTGACCCCCA A G SMIM20 Ensembl:ENSG00000250317 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1473072804 Functional Loss SNV dbSNP153 33..33 33 - - - 18431 RMVar_ID_18431 Human_SNP_ID_177397071 A-to-I Human chr4 + 26329193 26329193 26329193 TTTTGTATTTTCAGTAGAGACGGGGTTTCTCCATGTTGGTGAGACTGGTCTCGAACTCCTGACCT TTTTGTATTTTCAGTAGAGACGGGGTTTCTCCGTGTTGGTGAGACTGGTCTCGAACTCCTGACCT A G RBPJ Ensembl:ENSG00000168214 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1450194877 Functional Loss SNV dbSNP153 33..33 33 - - - 18432 RMVar_ID_18432 Human_SNP_ID_177398686 A-to-I Human chr4 + 26335830 26335830 26335830 TATTTTCAGTAGAGATGGGGTTTCACTGTGTTAGCCAGGATGGTCTCGAACTTCTGACCTTGTGA TATTTTCAGTAGAGATGGGGTTTCACTGTGTTGGCCAGGATGGTCTCGAACTTCTGACCTTGTGA A G RBPJ Ensembl:ENSG00000168214 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1293808745 Functional Loss SNV dbSNP153 33..33 33 - - - 18433 RMVar_ID_18433 Human_SNP_ID_177403699 A-to-I Human chr4 + 26355466 26355466 26355466 GTCCAGGAATTTGAGACCATCCTGGGCAACATAGCAAGACTTCATCTCTACCAAAAAAAAAAAAA GTCCAGGAATTTGAGACCATCCTGGGCAACATGGCAAGACTTCATCTCTACCAAAAAAAAAAAAA A G RBPJ Ensembl:ENSG00000168214 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1196683644 Functional Loss SNV dbSNP153 33..33 33 - - - 18434 RMVar_ID_18434 Human_SNP_ID_177501509 A-to-I Human chr4 + 26757198 26757197 26757199 ATAACACCTGGCTAAGTTTTTGTATTTTTAGTAGAGACAGGTTTTCACTACGTTGGCCAACCAGG ATAACACCTGGCTAAGTTTTTGTATTTTTAGT__AGACAGGTTTTCACTACGTTGGCCAACCAGG TAG T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971518957 Functional Loss DEL dbSNP153 33..34 33 - - - 18435 RMVar_ID_18435 Human_SNP_ID_177501510 A-to-I Human chr4 + 26757198 26757198 26757198 ATAACACCTGGCTAAGTTTTTGTATTTTTAGTAGAGACAGGTTTTCACTACGTTGGCCAACCAGG ATAACACCTGGCTAAGTTTTTGTATTTTTAGTGGAGACAGGTTTTCACTACGTTGGCCAACCAGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs766697905 Functional Loss SNV dbSNP153 33..33 33 - - - 18436 RMVar_ID_18436 Human_SNP_ID_177507963 A-to-I Human chr4 + 26787122 26787122 26787122 AAGAGGAACTAGTTTTTTTTTTTTTTTTTTTGAGATGGAATCTTACTCTGTAGCCCAAGCTGGTG AAGAGGAACTAGTTTTTTTTTTTTTTTTTTTGTGATGGAATCTTACTCTGTAGCCCAAGCTGGTG A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1371714056 Functional Loss SNV dbSNP153 33..33 33 - - - 18437 RMVar_ID_18437 Human_SNP_ID_330208652 A-to-I Human chr7 + 90370155 90370155 90370155 AACCTATATGGAAACAGTATGGAGATTTCTCAAAGAACTGAAAGTAGAAATATCATTTCATCCAG AACCTATATGGAAACAGTATGGAGATTTCTCAGAGAACTGAAAGTAGAAATATCATTTCATCCAG A G GTPBP10 Ensembl:ENSG00000105793 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1307458346 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60712,RMVar_hsa_circ_358317,RMVar_hsa_circ_246311,RMVar_hsa_circ_246312,RMVar_hsa_circ_307298 18438 RMVar_ID_18438 Human_SNP_ID_330212638 A-to-I Human chr7 + 90385900 90385900 90385900 CAACATGGCGAAACCCCGTCTCTACTAAAAATATAAAAAATTAGCCAGGCATAGTGGCGCATGCC CAACATGGCGAAACCCCGTCTCTACTAAAAATGTAAAAAATTAGCCAGGCATAGTGGCGCATGCC A G CLDN12,GTPBP10 Ensembl:ENSG00000157224,Ensembl:ENSG00000105793 Protein coding,Protein coding intron,3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1387232557 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4950869 18439 RMVar_ID_18439 Human_SNP_ID_330212642 A-to-I Human chr7 + 90385914 90385914 90385914 CCCGTCTCTACTAAAAATATAAAAAATTAGCCAGGCATAGTGGCGCATGCCTGTTGTAGCCCCAG CCCGTCTCTACTAAAAATATAAAAAATTAGCCGGGCATAGTGGCGCATGCCTGTTGTAGCCCCAG A G CLDN12,GTPBP10 Ensembl:ENSG00000157224,Ensembl:ENSG00000105793 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1299832636 Functional Loss SNV dbSNP153 33..33 33 - - - 18440 RMVar_ID_18440 Human_SNP_ID_330212650 A-to-I Human chr7 + 90385949 90385949 90385949 CATAGTGGCGCATGCCTGTTGTAGCCCCAGCTACTCAAGAGGCTGAGGCAGGAGAATTGCTTGAA CATAGTGGCGCATGCCTGTTGTAGCCCCAGCTGCTCAAGAGGCTGAGGCAGGAGAATTGCTTGAA A G CLDN12,GTPBP10 Ensembl:ENSG00000157224,Ensembl:ENSG00000105793 Protein coding,Protein coding intron,3'UTR GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,31158229,32596459 RNA-Seq:(High) rs1030461317 Functional Loss SNV dbSNP153 33..33 33 - - - 18441 RMVar_ID_18441 Human_SNP_ID_330212665 A-to-I Human chr7 + 90386001 90386001 90386001 AGAATTGCTTGAACGCGGGAGGTGGAGGATACAATGAACCCGAGGTCGCGCCACTGCACTTCAGC AGAATTGCTTGAACGCGGGAGGTGGAGGATACGATGAACCCGAGGTCGCGCCACTGCACTTCAGC A G CLDN12,GTPBP10 Ensembl:ENSG00000157224,Ensembl:ENSG00000105793 Protein coding,Protein coding intron,3'UTR GSE38233;GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,32596459 RNA-Seq:(High) rs1352487733 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16238783,Human_RBP_ID_18886754,Human_RBP_ID_26122244 18442 RMVar_ID_18442 Human_SNP_ID_330212817 A-to-I Human chr7 + 90386577 90386577 90386577 GCAGGCCAGGCATGGTGGTGCAGGCCAGACATAGCGGTACATGCCTGTAATCCTAGCACTTTGGG GCAGGCCAGGCATGGTGGTGCAGGCCAGACATGGCGGTACATGCCTGTAATCCTAGCACTTTGGG A G CLDN12,GTPBP10 Ensembl:ENSG00000157224,Ensembl:ENSG00000105793 Protein coding,Protein coding intron,3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1255959167 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7766092,Human_RBP_ID_8218980,Human_RBP_ID_16238797 18443 RMVar_ID_18443 Human_SNP_ID_330213546 A-to-I Human chr7 + 90389446 90389446 90389446 GTCTCGCTCTCTTGCCAGGCTGGAGTGCAGTGACATTATCTTGGCTCACTGCAGCCTCTGATTCC GTCTCGCTCTCTTGCCAGGCTGGAGTGCAGTGGCATTATCTTGGCTCACTGCAGCCTCTGATTCC A G CLDN12,GTPBP10 Ensembl:ENSG00000157224,Ensembl:ENSG00000105793 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1158441054 Functional Loss SNV dbSNP153 33..33 33 - - - 18444 RMVar_ID_18444 Human_SNP_ID_330213548 A-to-I Human chr7 + 90389451 90389451 90389451 GCTCTCTTGCCAGGCTGGAGTGCAGTGACATTATCTTGGCTCACTGCAGCCTCTGATTCCCTGGT GCTCTCTTGCCAGGCTGGAGTGCAGTGACATTTTCTTGGCTCACTGCAGCCTCTGATTCCCTGGT A T CLDN12,GTPBP10 Ensembl:ENSG00000157224,Ensembl:ENSG00000105793 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1362187365 Functional Loss SNV dbSNP153 33..33 33 - - - 18445 RMVar_ID_18445 Human_SNP_ID_330213563 A-to-I Human chr7 + 90389526 90389526 90389526 CTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCATCCACCACCACGTCCAGCTAATTTTT CTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTGCAGGCATCCACCACCACGTCCAGCTAATTTTT A G CLDN12,GTPBP10 Ensembl:ENSG00000157224,Ensembl:ENSG00000105793 Protein coding,Protein coding intron,3'UTR GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1285354223 Functional Loss SNV dbSNP153 33..33 33 - - - 18446 RMVar_ID_18446 Human_SNP_ID_330213686 A-to-I Human chr7 + 90389927 90389927 90389927 CTCCTGCCTCATCCTCCCAAGTAGCTAGGACTACAAGTGTGTGCCACCATACCTGGCTAATTTTT CTCCTGCCTCATCCTCCCAAGTAGCTAGGACTGCAAGTGTGTGCCACCATACCTGGCTAATTTTT A G CLDN12,GTPBP10 Ensembl:ENSG00000157224,Ensembl:ENSG00000105793 Protein coding,Protein coding intron,3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,31158229,31158229,31158229 RNA-Seq:(High) rs1360942499 Functional Loss SNV dbSNP153 33..33 33 - - - 18447 RMVar_ID_18447 Human_SNP_ID_330213699 A-to-I Human chr7 + 90389980 90389979 90389981 TGGCTAATTTTTAAAAACTATTTTGTAGAGACAGGGTCTTACTATGTTGCCCAGAGTGGTCTTGA TGGCTAATTTTTAAAAACTATTTTGTAGAGAC__GGTCTTACTATGTTGCCCAGAGTGGTCTTGA CAG C CLDN12,GTPBP10 Ensembl:ENSG00000157224,Ensembl:ENSG00000105793 Protein coding,Protein coding intron,3'UTR GSE38233;GSE100210;GSE99789;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,29796672,31158229,31158229 RNA-Seq:(High) rs1329861480 Functional Loss DEL dbSNP153 33..34 33 - - - 18448 RMVar_ID_18448 Human_SNP_ID_330213701 A-to-I Human chr7 + 90389991 90389991 90389991 TAAAAACTATTTTGTAGAGACAGGGTCTTACTATGTTGCCCAGAGTGGTCTTGAACTCCCATCCT TAAAAACTATTTTGTAGAGACAGGGTCTTACTCTGTTGCCCAGAGTGGTCTTGAACTCCCATCCT A C CLDN12,GTPBP10 Ensembl:ENSG00000157224,Ensembl:ENSG00000105793 Protein coding,Protein coding intron,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs138233300 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16238871 18449 RMVar_ID_18449 Human_SNP_ID_330213702 A-to-I Human chr7 + 90389991 90389991 90389991 TAAAAACTATTTTGTAGAGACAGGGTCTTACTATGTTGCCCAGAGTGGTCTTGAACTCCCATCCT TAAAAACTATTTTGTAGAGACAGGGTCTTACTGTGTTGCCCAGAGTGGTCTTGAACTCCCATCCT A G CLDN12,GTPBP10 Ensembl:ENSG00000157224,Ensembl:ENSG00000105793 Protein coding,Protein coding intron,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs138233300 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16238871 18450 RMVar_ID_18450 Human_SNP_ID_330213714 A-to-I Human chr7 + 90390043 90390043 90390043 GAACTCCCATCCTCATGGAATCCTCCCACTTCAGTCTCTGAAAGTGCTAGGATTATAGGCATGAG GAACTCCCATCCTCATGGAATCCTCCCACTTCGGTCTCTGAAAGTGCTAGGATTATAGGCATGAG A G CLDN12,GTPBP10 Ensembl:ENSG00000157224,Ensembl:ENSG00000105793 Protein coding,Protein coding intron,3'UTR GSE38233;GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs555435226 Functional Loss SNV dbSNP153 33..33 33 - - - 18451 RMVar_ID_18451 Human_SNP_ID_330213718 A-to-I Human chr7 + 90390071 90390071 90390071 CTTCAGTCTCTGAAAGTGCTAGGATTATAGGCATGAGCCATTTATGCCCAGCCAGTTTTCTTTTT CTTCAGTCTCTGAAAGTGCTAGGATTATAGGCGTGAGCCATTTATGCCCAGCCAGTTTTCTTTTT A G CLDN12,GTPBP10 Ensembl:ENSG00000157224,Ensembl:ENSG00000105793 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs779480422 Functional Loss SNV dbSNP153 33..33 33 - - - 18452 RMVar_ID_18452 Human_SNP_ID_330218243 A-to-I Human chr7 + 90408982 90408982 90408982 TGGGGTCTCGCTATGTTGCCCAATCTGGTCTCAAACTCCTGGGCTCAAGCTATCCTCCCACCGCA TGGGGTCTCGCTATGTTGCCCAATCTGGTCTCGAACTCCTGGGCTCAAGCTATCCTCCCACCGCA A G AC006153.1,CLDN12 Ensembl:ENSG00000273299,Ensembl:ENSG00000157224 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417593307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_886954 18453 RMVar_ID_18453 Human_SNP_ID_330622023 A-to-I Human chr7 + 92081383 92081383 92081383 TGGAGTTCAGTGGTGTGATCTCAGCTCACTGCAGCCTCCACCTCCTGGGTTTCCAGCAATTCTCC TGGAGTTCAGTGGTGTGATCTCAGCTCACTGCGGCCTCCACCTCCTGGGTTTCCAGCAATTCTCC A G AKAP9 Ensembl:ENSG00000127914 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459603689 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120283,RMVar_hsa_circ_246352,RMVar_hsa_circ_46765,RMVar_hsa_circ_58955,RMVar_hsa_circ_63410,RMVar_hsa_circ_346055,RMVar_hsa_circ_331365,RMVar_hsa_circ_246382,RMVar_hsa_circ_14213,RMVar_hsa_circ_345375,RMVar_hsa_circ_59984,RMVar_hsa_circ_17206,RMVar_hsa_circ_246387,RMVar_hsa_circ_284693,RMVar_hsa_circ_314676,RMVar_hsa_circ_21072,RMVar_hsa_circ_309250,RMVar_hsa_circ_280570,RMVar_hsa_circ_246388,RMVar_hsa_circ_246385,RMVar_hsa_circ_246386,RMVar_hsa_circ_317836,RMVar_hsa_circ_64643,RMVar_hsa_circ_5553,RMVar_hsa_circ_246389,RMVar_hsa_circ_327075,RMVar_hsa_circ_30233,RMVar_hsa_circ_246391,RMVar_hsa_circ_364495,RMVar_hsa_circ_246392,RMVar_hsa_circ_23669 18454 RMVar_ID_18454 Human_SNP_ID_330624404 A-to-I Human chr7 + 92090516 92090516 92090516 GTGGTGGCGGGTGCCTGTAAGGCCAGCCACTCAGGAGACTGAAGCAGAGAATTACTTGAACCCAG GTGGTGGCGGGTGCCTGTAAGGCCAGCCACTCGGGAGACTGAAGCAGAGAATTACTTGAACCCAG A G AKAP9 Ensembl:ENSG00000127914 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1228492410 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16241316 RMVar_hsa_circ_3884,RMVar_hsa_circ_120283,RMVar_hsa_circ_246352,RMVar_hsa_circ_59984,RMVar_hsa_circ_246387,RMVar_hsa_circ_314676,RMVar_hsa_circ_21072,RMVar_hsa_circ_309250,RMVar_hsa_circ_246388,RMVar_hsa_circ_5553,RMVar_hsa_circ_246392,RMVar_hsa_circ_47216,RMVar_hsa_circ_246394,RMVar_hsa_circ_31055,RMVar_hsa_circ_301932 18455 RMVar_ID_18455 Human_SNP_ID_330624640 A-to-I Human chr7 + 92091551 92091551 92091551 GAGGTTGCAATGAGTTGGGATCGTGCCATTGTACTCCAGCTTGGACGACAGGGCAAGACTCTGTC GAGGTTGCAATGAGTTGGGATCGTGCCATTGTGCTCCAGCTTGGACGACAGGGCAAGACTCTGTC A G AKAP9 Ensembl:ENSG00000127914 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1206476580 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26122889 RMVar_hsa_circ_3884,RMVar_hsa_circ_120283,RMVar_hsa_circ_246352,RMVar_hsa_circ_59984,RMVar_hsa_circ_246387,RMVar_hsa_circ_314676,RMVar_hsa_circ_21072,RMVar_hsa_circ_309250,RMVar_hsa_circ_246388,RMVar_hsa_circ_5553,RMVar_hsa_circ_246392,RMVar_hsa_circ_47216,RMVar_hsa_circ_246394,RMVar_hsa_circ_31055,RMVar_hsa_circ_301932 18456 RMVar_ID_18456 Human_SNP_ID_330624941 A-to-I Human chr7 + 92092708 92092708 92092708 TCTCACTGTCACTGAGGCTGGAGTACAGTGGCATGGTCTCAACTCATTGCAACCTCCACCTCCCG TCTCACTGTCACTGAGGCTGGAGTACAGTGGCGTGGTCTCAACTCATTGCAACCTCCACCTCCCG A G AKAP9 Ensembl:ENSG00000127914 Protein coding intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1215466499 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3884,RMVar_hsa_circ_120283,RMVar_hsa_circ_246352,RMVar_hsa_circ_59984,RMVar_hsa_circ_246387,RMVar_hsa_circ_314676,RMVar_hsa_circ_21072,RMVar_hsa_circ_309250,RMVar_hsa_circ_246388,RMVar_hsa_circ_5553,RMVar_hsa_circ_246392,RMVar_hsa_circ_47216,RMVar_hsa_circ_246394,RMVar_hsa_circ_31055,RMVar_hsa_circ_301932 18457 RMVar_ID_18457 Human_SNP_ID_330624960 A-to-I Human chr7 + 92092764 92092764 92092764 CACCTCCCGGGCTCAAGCAATCCCCCCACCTCAGCCTCCTGAGTCGATGGGACTACAGGCACATG CACCTCCCGGGCTCAAGCAATCCCCCCACCTCGGCCTCCTGAGTCGATGGGACTACAGGCACATG A G AKAP9 Ensembl:ENSG00000127914 Protein coding intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs920748869 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3884,RMVar_hsa_circ_120283,RMVar_hsa_circ_246352,RMVar_hsa_circ_59984,RMVar_hsa_circ_246387,RMVar_hsa_circ_314676,RMVar_hsa_circ_21072,RMVar_hsa_circ_309250,RMVar_hsa_circ_246388,RMVar_hsa_circ_5553,RMVar_hsa_circ_246392,RMVar_hsa_circ_47216,RMVar_hsa_circ_246394,RMVar_hsa_circ_31055,RMVar_hsa_circ_301932 18458 RMVar_ID_18458 Human_SNP_ID_330650823 A-to-I Human chr7 - 92197163 92197163 92197163 ACCAATTATCCTGCCTCATCAGCCTCCTGAGTAGCTGGGATTACAGACGTGCGCCACCATGCCCA ACCAATTATCCTGCCTCATCAGCCTCCTGAGTGGCTGGGATTACAGACGTGCGCCACCATGCCCA T C AC000120.4 Ensembl:ENSG00000285953 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1390666579 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_246409 18459 RMVar_ID_18459 Human_SNP_ID_330651510 A-to-I Human chr7 - 92200431 92200431 92200431 GAGATCGCTTAAACCCAGGAGGTGGAGGTTGTAGTGAGCCAAGATTGCACCACGGCACGCTAGCC GAGATCGCTTAAACCCAGGAGGTGGAGGTTGTGGTGAGCCAAGATTGCACCACGGCACGCTAGCC T C AC000120.2,KRIT1,AC000120.4 Ensembl:ENSG00000243107,Ensembl:ENSG00000001631,Ensembl:ENSG00000285953 lincRNA,Protein coding,Protein coding exon,3'UTR,intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1236687238 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8273426 Human_Splice_Rec_888292 RMVar_hsa_circ_246409 18460 RMVar_ID_18460 Human_SNP_ID_330651523 A-to-I Human chr7 - 92200494 92200494 92200494 CAAAAATTAGCTGGGTGTGGTGGCGGGCGCCTATAATCCTAGCTACTAGGGAGGCCAAGGTGGGA CAAAAATTAGCTGGGTGTGGTGGCGGGCGCCTGTAATCCTAGCTACTAGGGAGGCCAAGGTGGGA T C AC000120.2,KRIT1,AC000120.4 Ensembl:ENSG00000243107,Ensembl:ENSG00000001631,Ensembl:ENSG00000285953 lincRNA,Protein coding,Protein coding intron,3'UTR,intron GSE100210;GSE107867 HepG2 cell line;ASD brains,frontal_cortex - 29129909,30559470 RNA-Seq:(High) rs1213844086 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26122994 RMVar_hsa_circ_246409 18461 RMVar_ID_18461 Human_SNP_ID_330651539 A-to-I Human chr7 - 92200569 92200569 92200569 GGCAGGCGGATCACCTGAAGTCAGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCCTGTCTC GGCAGGCGGATCACCTGAAGTCAGAGTTCAAGCCCAGCCTGGCCAACATGGTGAAACCCTGTCTC T G AC000120.2,KRIT1,AC000120.4 Ensembl:ENSG00000243107,Ensembl:ENSG00000001631,Ensembl:ENSG00000285953 lincRNA,Protein coding,Protein coding intron,3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991965771 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_175931,Human_RBP_ID_8220622 RMVar_hsa_circ_246409 18462 RMVar_ID_18462 Human_SNP_ID_330658084 A-to-I Human chr7 - 92227699 92227699 92227699 GAAACCCCATCTTTACTAAAGACACAAAAATTAGCTGGGCGTGGTGGCGCATGCCTGTAATCCCA GAAACCCCATCTTTACTAAAGACACAAAAATTCGCTGGGCGTGGTGGCGCATGCCTGTAATCCCA T G KRIT1,AC000120.4 Ensembl:ENSG00000001631,Ensembl:ENSG00000285953 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs942889441 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5300,RMVar_hsa_circ_246409,RMVar_hsa_circ_300597,RMVar_hsa_circ_346615,RMVar_hsa_circ_363801,RMVar_hsa_circ_360437,RMVar_hsa_circ_8509,RMVar_hsa_circ_6270,RMVar_hsa_circ_246415,RMVar_hsa_circ_246411,RMVar_hsa_circ_246410,RMVar_hsa_circ_322014,RMVar_hsa_circ_344308,RMVar_hsa_circ_377654,RMVar_hsa_circ_338619,RMVar_hsa_circ_322282,RMVar_hsa_circ_300571,RMVar_hsa_circ_313384,RMVar_hsa_circ_292544,RMVar_hsa_circ_9409,RMVar_hsa_circ_58843,RMVar_hsa_circ_246420,RMVar_hsa_circ_246422,RMVar_hsa_circ_246423,RMVar_hsa_circ_246421,RMVar_hsa_circ_246419,RMVar_hsa_circ_43538,RMVar_hsa_circ_314917,RMVar_hsa_circ_35203,RMVar_hsa_circ_269547,RMVar_hsa_circ_362901,RMVar_hsa_circ_356585,RMVar_hsa_circ_9994,RMVar_hsa_circ_318276,RMVar_hsa_circ_63802,RMVar_hsa_circ_63573,RMVar_hsa_circ_246424,RMVar_hsa_circ_39064,RMVar_hsa_circ_311945,RMVar_hsa_circ_304173,RMVar_hsa_circ_283559,RMVar_hsa_circ_246428,RMVar_hsa_circ_63180,RMVar_hsa_circ_246429,RMVar_hsa_circ_345623 18463 RMVar_ID_18463 Human_SNP_ID_330686392 A-to-I Human chr7 + 92347468 92347468 92347468 AAGGGCTGAAATAAAAGGGAATAGCCAGGCATAGTGGCACATGTCTGTAGTCCTAGCTACTTGGG AAGGGCTGAAATAAAAGGGAATAGCCAGGCATGGTGGCACATGTCTGTAGTCCTAGCTACTTGGG A G ANKIB1 Ensembl:ENSG00000001629 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1011985188 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16293182 RMVar_hsa_circ_246451,RMVar_hsa_circ_246434,RMVar_hsa_circ_292607,RMVar_hsa_circ_79243,RMVar_hsa_circ_367120,RMVar_hsa_circ_246433,RMVar_hsa_circ_287682,RMVar_hsa_circ_279913,RMVar_hsa_circ_95605,RMVar_hsa_circ_88132,RMVar_hsa_circ_246438,RMVar_hsa_circ_246436,RMVar_hsa_circ_246437,RMVar_hsa_circ_246435,RMVar_hsa_circ_56937,RMVar_hsa_circ_349811,RMVar_hsa_circ_294219,RMVar_hsa_circ_297685,RMVar_hsa_circ_360730,RMVar_hsa_circ_246449,RMVar_hsa_circ_246450,RMVar_hsa_circ_246448,RMVar_hsa_circ_302728,RMVar_hsa_circ_347849,RMVar_hsa_circ_284842,RMVar_hsa_circ_246453,RMVar_hsa_circ_279816,RMVar_hsa_circ_246452,RMVar_hsa_circ_108290,RMVar_hsa_circ_246457,RMVar_hsa_circ_289508,RMVar_hsa_circ_246455,RMVar_hsa_circ_246454,RMVar_hsa_circ_303479,RMVar_hsa_circ_337548,RMVar_hsa_circ_298553,RMVar_hsa_circ_27317,RMVar_hsa_circ_44248,RMVar_hsa_circ_246458,RMVar_hsa_circ_246459,RMVar_hsa_circ_125004,RMVar_hsa_circ_282850,RMVar_hsa_circ_246456,RMVar_hsa_circ_287504,RMVar_hsa_circ_277037,RMVar_hsa_circ_122464,RMVar_hsa_circ_246461,RMVar_hsa_circ_246463,RMVar_hsa_circ_246465,RMVar_hsa_circ_51544,RMVar_hsa_circ_246464,RMVar_hsa_circ_246462,RMVar_hsa_circ_246460 18464 RMVar_ID_18464 Human_SNP_ID_330686393 A-to-I Human chr7 + 92347468 92347468 92347468 AAGGGCTGAAATAAAAGGGAATAGCCAGGCATAGTGGCACATGTCTGTAGTCCTAGCTACTTGGG AAGGGCTGAAATAAAAGGGAATAGCCAGGCATTGTGGCACATGTCTGTAGTCCTAGCTACTTGGG A T ANKIB1 Ensembl:ENSG00000001629 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1011985188 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16293182 RMVar_hsa_circ_246451,RMVar_hsa_circ_246434,RMVar_hsa_circ_292607,RMVar_hsa_circ_79243,RMVar_hsa_circ_367120,RMVar_hsa_circ_246433,RMVar_hsa_circ_287682,RMVar_hsa_circ_279913,RMVar_hsa_circ_95605,RMVar_hsa_circ_88132,RMVar_hsa_circ_246438,RMVar_hsa_circ_246436,RMVar_hsa_circ_246437,RMVar_hsa_circ_246435,RMVar_hsa_circ_56937,RMVar_hsa_circ_349811,RMVar_hsa_circ_294219,RMVar_hsa_circ_297685,RMVar_hsa_circ_360730,RMVar_hsa_circ_246449,RMVar_hsa_circ_246450,RMVar_hsa_circ_246448,RMVar_hsa_circ_302728,RMVar_hsa_circ_347849,RMVar_hsa_circ_284842,RMVar_hsa_circ_246453,RMVar_hsa_circ_279816,RMVar_hsa_circ_246452,RMVar_hsa_circ_108290,RMVar_hsa_circ_246457,RMVar_hsa_circ_289508,RMVar_hsa_circ_246455,RMVar_hsa_circ_246454,RMVar_hsa_circ_303479,RMVar_hsa_circ_337548,RMVar_hsa_circ_298553,RMVar_hsa_circ_27317,RMVar_hsa_circ_44248,RMVar_hsa_circ_246458,RMVar_hsa_circ_246459,RMVar_hsa_circ_125004,RMVar_hsa_circ_282850,RMVar_hsa_circ_246456,RMVar_hsa_circ_287504,RMVar_hsa_circ_277037,RMVar_hsa_circ_122464,RMVar_hsa_circ_246461,RMVar_hsa_circ_246463,RMVar_hsa_circ_246465,RMVar_hsa_circ_51544,RMVar_hsa_circ_246464,RMVar_hsa_circ_246462,RMVar_hsa_circ_246460 18465 RMVar_ID_18465 Human_SNP_ID_330690960 A-to-I Human chr7 + 92366566 92366566 92366566 GATCTTTTAGGTTTATATAGTCCTTCTCTGGTAGAACAAATCTCAGGTGTCTTCAGTCTTTTGTC GATCTTTTAGGTTTATATAGTCCTTCTCTGGTGGAACAAATCTCAGGTGTCTTCAGTCTTTTGTC A G ANKIB1 Ensembl:ENSG00000001629 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs181322820 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_66 RMVar_hsa_circ_1568,RMVar_hsa_circ_246434,RMVar_hsa_circ_79243,RMVar_hsa_circ_367120,RMVar_hsa_circ_246433,RMVar_hsa_circ_287682,RMVar_hsa_circ_88132,RMVar_hsa_circ_246435,RMVar_hsa_circ_56937,RMVar_hsa_circ_297685,RMVar_hsa_circ_246450,RMVar_hsa_circ_302728,RMVar_hsa_circ_347849,RMVar_hsa_circ_246453,RMVar_hsa_circ_108290,RMVar_hsa_circ_289508,RMVar_hsa_circ_337548,RMVar_hsa_circ_27317,RMVar_hsa_circ_44248,RMVar_hsa_circ_246458,RMVar_hsa_circ_246459,RMVar_hsa_circ_125004,RMVar_hsa_circ_282850,RMVar_hsa_circ_122464,RMVar_hsa_circ_246463,RMVar_hsa_circ_246465,RMVar_hsa_circ_246464,RMVar_hsa_circ_246462,RMVar_hsa_circ_317371,RMVar_hsa_circ_360357,RMVar_hsa_circ_367082,RMVar_hsa_circ_38998,RMVar_hsa_circ_5837,RMVar_hsa_circ_24878,RMVar_hsa_circ_246467,RMVar_hsa_circ_246468,RMVar_hsa_circ_346270,RMVar_hsa_circ_74979,RMVar_hsa_circ_23516,RMVar_hsa_circ_246473,RMVar_hsa_circ_77493,RMVar_hsa_circ_324227,RMVar_hsa_circ_246474,RMVar_hsa_circ_246475 18466 RMVar_ID_18466 Human_SNP_ID_330690970 A-to-I Human chr7 + 92366603 92366603 92366603 AAATCTCAGGTGTCTTCAGTCTTTTGTCTCCTATCATGTTTTCAAACATTCTTCCATCTTTCCAA AAATCTCAGGTGTCTTCAGTCTTTTGTCTCCTGTCATGTTTTCAAACATTCTTCCATCTTTCCAA A G ANKIB1 Ensembl:ENSG00000001629 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs114801083 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_67,Clinvar_Rec_68,Clinvar_Rec_69 RMVar_hsa_circ_1568,RMVar_hsa_circ_246434,RMVar_hsa_circ_79243,RMVar_hsa_circ_367120,RMVar_hsa_circ_246433,RMVar_hsa_circ_287682,RMVar_hsa_circ_88132,RMVar_hsa_circ_246435,RMVar_hsa_circ_56937,RMVar_hsa_circ_297685,RMVar_hsa_circ_246450,RMVar_hsa_circ_302728,RMVar_hsa_circ_347849,RMVar_hsa_circ_246453,RMVar_hsa_circ_108290,RMVar_hsa_circ_289508,RMVar_hsa_circ_337548,RMVar_hsa_circ_27317,RMVar_hsa_circ_44248,RMVar_hsa_circ_246458,RMVar_hsa_circ_246459,RMVar_hsa_circ_125004,RMVar_hsa_circ_282850,RMVar_hsa_circ_122464,RMVar_hsa_circ_246463,RMVar_hsa_circ_246465,RMVar_hsa_circ_246464,RMVar_hsa_circ_246462,RMVar_hsa_circ_317371,RMVar_hsa_circ_360357,RMVar_hsa_circ_367082,RMVar_hsa_circ_38998,RMVar_hsa_circ_5837,RMVar_hsa_circ_24878,RMVar_hsa_circ_246467,RMVar_hsa_circ_246468,RMVar_hsa_circ_346270,RMVar_hsa_circ_74979,RMVar_hsa_circ_23516,RMVar_hsa_circ_246473,RMVar_hsa_circ_77493,RMVar_hsa_circ_324227,RMVar_hsa_circ_246474,RMVar_hsa_circ_246475 18467 RMVar_ID_18467 Human_SNP_ID_330720847 A-to-I Human chr7 + 92492402 92492402 92492402 TGCAACCATGATTTGGTCTCAAACTAGGCCCAAATGATCCTCCTGCCTTGGCCTGCCAAAGTGCT TGCAACCATGATTTGGTCTCAAACTAGGCCCAGATGATCCTCCTGCCTTGGCCTGCCAAAGTGCT A G AC007566.1 Ensembl:ENSG00000244055 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1220977886 Functional Loss SNV dbSNP153 33..33 33 - - - 18468 RMVar_ID_18468 Human_SNP_ID_330721261 A-to-I Human chr7 - 92494047 92494047 92494047 CTGTGTTGGCTGATTGGGGAAAAAAAAATGCAAGAAACCTAATGTATTATATTTTCACATTATCT CTGTGTTGGCTGATTGGGGAAAAAAAAATGCAGGAAACCTAATGTATTATATTTTCACATTATCT T C PEX1 Ensembl:ENSG00000127980 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1189760530 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1114786,Human_RBP_ID_23078970 RMVar_hsa_circ_57420,RMVar_hsa_circ_15892,RMVar_hsa_circ_55728,RMVar_hsa_circ_99148,RMVar_hsa_circ_246487,RMVar_hsa_circ_332726,RMVar_hsa_circ_11792,RMVar_hsa_circ_27824,RMVar_hsa_circ_246488,RMVar_hsa_circ_246489,RMVar_hsa_circ_38952 18469 RMVar_ID_18469 Human_SNP_ID_330732586 A-to-I Human chr7 + 92539578 92539578 92539578 ACAAAAAGCCAGGCGTGGTGGCAAATGCCTATAATCCCAGCTACTCGGGAGGCTGAGGCATGAGA ACAAAAAGCCAGGCGTGGTGGCAAATGCCTATGATCCCAGCTACTCGGGAGGCTGAGGCATGAGA A G RBM48 Ensembl:ENSG00000127993 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1171505187 Functional Loss SNV dbSNP153 33..33 33 - - - 18470 RMVar_ID_18470 Human_SNP_ID_330732597 A-to-I Human chr7 + 92539619 92539613 92539619 TACTCGGGAGGCTGAGGCATGAGAATTACTTGAACCCAGGAGGCAGAGATCGCAGTGAGTTGAGA TACTCGGGAGGCTGAGGCATGAGAATT______ACCCAGGAGGCAGAGATCGCAGTGAGTTGAGA TACTTGA T RBM48 Ensembl:ENSG00000127993 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1470390092 Functional Loss DEL dbSNP153 28..33 33 - - - 18471 RMVar_ID_18471 Human_SNP_ID_330739602 A-to-I Human chr7 - 92567110 92567110 92567110 TGGGCTCAAGTGATTTTCCACTTCACCCTTCCAAGTAGCTAGGACTACAGTCACATGCCACCACA TGGGCTCAAGTGATTTTCCACTTCACCCTTCCGAGTAGCTAGGACTACAGTCACATGCCACCACA T C FAM133B Ensembl:ENSG00000234545 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256835539 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_356442 18472 RMVar_ID_18472 Human_SNP_ID_330741074 A-to-I Human chr7 - 92573265 92573265 92573265 TTCTCCCGAGACTGAAGTGGGAGGATCACTTAAGCCCAGAAATTGGAGGTTACAGTGAGTTATGA TTCTCCCGAGACTGAAGTGGGAGGATCACTTACGCCCAGAAATTGGAGGTTACAGTGAGTTATGA T G FAM133B Ensembl:ENSG00000234545 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs575242709 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_354235,RMVar_hsa_circ_356442,RMVar_hsa_circ_310251 18473 RMVar_ID_18473 Human_SNP_ID_330761792 A-to-I Human chr7 - 92664960 92664960 92664960 TAATACAGTGAAAACCCGTCTCTATTAAAAATACAAAAAATTAGCTGAGCGTGGTGGCATGCTCC TAATACAGTGAAAACCCGTCTCTATTAAAAATGCAAAAAATTAGCTGAGCGTGGTGGCATGCTCC T C CDK6 Ensembl:ENSG00000105810 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1332385236 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_174006,Human_RBP_ID_3111250 RMVar_hsa_circ_16943,RMVar_hsa_circ_83185,RMVar_hsa_circ_94806,RMVar_hsa_circ_246509,RMVar_hsa_circ_246510,RMVar_hsa_circ_78756,RMVar_hsa_circ_246512 18474 RMVar_ID_18474 Human_SNP_ID_330770826 A-to-I Human chr7 - 92704673 92704673 92704673 CCACAATAGAATTACACAGCAGTGAAAATTTAAAAATGAATGAGCTATAGCTACAGGCAATAACA CCACAATAGAATTACACAGCAGTGAAAATTTATAAATGAATGAGCTATAGCTACAGGCAATAACA T A CDK6 Ensembl:ENSG00000105810 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs778830803 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3111721 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 18475 RMVar_ID_18475 Human_SNP_ID_330912401 A-to-I Human chr7 + 93318985 93318985 93318985 TTCATATATAGCAAAAGTAGAAAAGCAAGAGGAAAAATGATACACACAAGGTACGGCCCATTCCC TTCATATATAGCAAAAGTAGAAAAGCAAGAGGGAAAATGATACACACAAGGTACGGCCCATTCCC A G VPS50 Ensembl:ENSG00000004766 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1252856428 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_304578,RMVar_hsa_circ_301253,RMVar_hsa_circ_284446,RMVar_hsa_circ_7052,RMVar_hsa_circ_315273,RMVar_hsa_circ_21081,RMVar_hsa_circ_6236,RMVar_hsa_circ_246522,RMVar_hsa_circ_360962,RMVar_hsa_circ_307820,RMVar_hsa_circ_281957,RMVar_hsa_circ_374285,RMVar_hsa_circ_246524,RMVar_hsa_circ_246528,RMVar_hsa_circ_281762,RMVar_hsa_circ_246527,RMVar_hsa_circ_295551,RMVar_hsa_circ_24988,RMVar_hsa_circ_246531,RMVar_hsa_circ_246533,RMVar_hsa_circ_123157,RMVar_hsa_circ_306501,RMVar_hsa_circ_354513,RMVar_hsa_circ_365898,RMVar_hsa_circ_246534 18476 RMVar_ID_18476 Human_SNP_ID_331003703 A-to-I Human chr7 + 93706079 93706079 93706079 ATGTGCACAACATGCAGGTTTGTTACATAAGTATACATATGCTATGTCGGTTTGCTGCCCCCATT ATGTGCACAACATGCAGGTTTGTTACATAAGTTTACATATGCTATGTCGGTTTGCTGCCCCCATT A T GNGT1 Ensembl:ENSG00000127928 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985529056 Functional Loss SNV dbSNP153 33..33 33 - - - 18477 RMVar_ID_18477 Human_SNP_ID_331003704 A-to-I Human chr7 + 93706085 93706085 93706085 ACAACATGCAGGTTTGTTACATAAGTATACATATGCTATGTCGGTTTGCTGCCCCCATTAACTCG ACAACATGCAGGTTTGTTACATAAGTATACATGTGCTATGTCGGTTTGCTGCCCCCATTAACTCG A G GNGT1 Ensembl:ENSG00000127928 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215966657 Functional Loss SNV dbSNP153 33..33 33 - - - 18478 RMVar_ID_18478 Human_SNP_ID_331027498 A-to-I Human chr7 + 93812593 93812593 93812593 TGAAATTACTGACCGTACAAACAGTAATCTGTAAATATTTTGTTACTGTAGATTACAACAAAAGA TGAAATTACTGACCGTACAAACAGTAATCTGTGAATATTTTGTTACTGTAGATTACAACAAAAGA A G GNGT1 Ensembl:ENSG00000127928 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1237681486 Functional Loss SNV dbSNP153 33..33 33 - - - 18479 RMVar_ID_18479 Human_SNP_ID_331027508 A-to-I Human chr7 + 93812621 93812619 93812621 CTGTAAATATTTTGTTACTGTAGATTACAACAAAAGACTCTGGAAGCTGTTCAAATTGGGATACA CTGTAAATATTTTGTTACTGTAGATTACAAC__AAGACTCTGGAAGCTGTTCAAATTGGGATACA CAA C GNGT1 Ensembl:ENSG00000127928 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1456760250 Functional Loss DEL dbSNP153 32..33 33 - - - 18480 RMVar_ID_18480 Human_SNP_ID_331213350 A-to-I Human chr7 - 94596685 94596685 94596685 ATGAATGTGAAGATGAAATGCATGCCCTTTTAAGAAGGGTTAATTAATAAGTACAAGGCAGCATT ATGAATGTGAAGATGAAATGCATGCCCTTTTAGGAAGGGTTAATTAATAAGTACAAGGCAGCATT T C SGCE Ensembl:ENSG00000127990 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1452725351 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6322,RMVar_hsa_circ_33337,RMVar_hsa_circ_14304,RMVar_hsa_circ_330414,RMVar_hsa_circ_246670 18481 RMVar_ID_18481 Human_SNP_ID_331301643 A-to-I Human chr7 + 94990625 94990625 94990625 TGTATTATTGTTAAATGTATTCATTTTACAATACTATAGAACACTAGAATTTACTCTTCTTATCT TGTATTATTGTTAAATGTATTCATTTTACAATTCTATAGAACACTAGAATTTACTCTTCTTATCT A T PPP1R9A Ensembl:ENSG00000158528 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1046954482 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8148687 RMVar_hsa_circ_81915,RMVar_hsa_circ_69185,RMVar_hsa_circ_360571,RMVar_hsa_circ_246681 18482 RMVar_ID_18482 Human_SNP_ID_331301645 A-to-I Human chr7 + 94990628 94990628 94990628 ATTATTGTTAAATGTATTCATTTTACAATACTATAGAACACTAGAATTTACTCTTCTTATCTAGC ATTATTGTTAAATGTATTCATTTTACAATACTGTAGAACACTAGAATTTACTCTTCTTATCTAGC A G PPP1R9A Ensembl:ENSG00000158528 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1010352158 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8148687 RMVar_hsa_circ_81915,RMVar_hsa_circ_69185,RMVar_hsa_circ_360571,RMVar_hsa_circ_246681 18483 RMVar_ID_18483 Human_SNP_ID_331347846 A-to-I Human chr7 - 95187592 95187592 95187592 AAAAGTCCAACAGAGCACAAACAGACAATCTAAGGACACAACTCAAGGAACTAGAGAAAGAACAA AAAAGTCCAACAGAGCACAAACAGACAATCTAGGGACACAACTCAAGGAACTAGAGAAAGAACAA T C PPP1R9A-AS1 Ensembl:ENSG00000236197 lincRNA intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1286768152 Functional Loss SNV dbSNP153 33..33 33 - - - 18484 RMVar_ID_18484 Human_SNP_ID_331404867 A-to-I Human chr7 - 95433217 95433217 95433217 AAAACAAAATTTGAGTTGGTAATTTATAAACTATGGTGTCTACCTACCAGAGATTTTTCGTTATA AAAACAAAATTTGAGTTGGTAATTTATAAACTGTGGTGTCTACCTACCAGAGATTTTTCGTTATA T C PON2 Ensembl:ENSG00000105854 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs78118557 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3117118 18485 RMVar_ID_18485 Human_SNP_ID_331404900 A-to-I Human chr7 - 95433349 95433347 95433349 ACACCTGTAATCCCAGCACTGTTGGAGGCCTAAGCCAGAAGATTGCTTGAGCCCAGGAGTTAGTG ACACCTGTAATCCCAGCACTGTTGGAGGCCTA__CCAGAAGATTGCTTGAGCCCAGGAGTTAGTG GCT G PON2 Ensembl:ENSG00000105854 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1046784248 Functional Loss DEL dbSNP153 33..34 33 - - - 18486 RMVar_ID_18486 Human_SNP_ID_331405118 A-to-I Human chr7 - 95434265 95434265 95434265 CTATTCCATCTCGCATTTTAGTTTTAATGAAAATCTCTGGTAGGTAGACATCATCGTTTATAAAT CTATTCCATCTCGCATTTTAGTTTTAATGAAAGTCTCTGGTAGGTAGACATCATCGTTTATAAAT T C PON2 Ensembl:ENSG00000105854 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs925603846 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3117120 Human_Splice_Rec_892240,Human_Splice_Rec_892241,Human_Splice_Rec_892250,Human_Splice_Rec_892251 18487 RMVar_ID_18487 Human_SNP_ID_331499469 A-to-I Human chr7 + 95826090 95826090 95826090 AGCAGCATCTGTATGTCCTGGAGCGTGTTTGAAATGCAGAGTCTCGGGCCACCCGCACACCTACT AGCAGCATCTGTATGTCCTGGAGCGTGTTTGAGATGCAGAGTCTCGGGCCACCCGCACACCTACT A G DYNC1I1 Ensembl:ENSG00000158560 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs750695974 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_303877,RMVar_hsa_circ_335494,RMVar_hsa_circ_342369,RMVar_hsa_circ_327804,RMVar_hsa_circ_342376,RMVar_hsa_circ_246694,RMVar_hsa_circ_246695,RMVar_hsa_circ_364477 18488 RMVar_ID_18488 Human_SNP_ID_331547785 A-to-I Human chr7 + 96040786 96040786 96040786 CTCTGTCACCCAGGCTGGAGTGCAATGGCACTATCTTGGCTCACGGCAGCCTCTGCCTCCCAGGT CTCTGTCACCCAGGCTGGAGTGCAATGGCACTGTCTTGGCTCACGGCAGCCTCTGCCTCCCAGGT A G DYNC1I1 Ensembl:ENSG00000158560 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs542049934 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_214,RMVar_hsa_circ_20052,RMVar_hsa_circ_335494,RMVar_hsa_circ_338643,RMVar_hsa_circ_2626,RMVar_hsa_circ_246698,RMVar_hsa_circ_298253,RMVar_hsa_circ_246703,RMVar_hsa_circ_25991,RMVar_hsa_circ_246706,RMVar_hsa_circ_246711,RMVar_hsa_circ_329044 18489 RMVar_ID_18489 Human_SNP_ID_331547809 A-to-I Human chr7 + 96040931 96040931 96040931 TTTTAGTAGAGATGGGGTTTCGCATGTTGGCCAGGCTGGTCTTGAACTCCCAACCTCAAATGATC TTTTAGTAGAGATGGGGTTTCGCATGTTGGCCGGGCTGGTCTTGAACTCCCAACCTCAAATGATC A G DYNC1I1 Ensembl:ENSG00000158560 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1225209767 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_214,RMVar_hsa_circ_20052,RMVar_hsa_circ_335494,RMVar_hsa_circ_338643,RMVar_hsa_circ_2626,RMVar_hsa_circ_246698,RMVar_hsa_circ_298253,RMVar_hsa_circ_246703,RMVar_hsa_circ_25991,RMVar_hsa_circ_246706,RMVar_hsa_circ_246711,RMVar_hsa_circ_329044 18490 RMVar_ID_18490 Human_SNP_ID_331569732 A-to-I Human chr7 - 96133869 96133869 96133869 TTGCCCTGGCTGGAATGCAGTGGCATGATCTCAGCTCACTACAACCTCCACCTCCGGGTTCAAGC TTGCCCTGGCTGGAATGCAGTGGCATGATCTCGGCTCACTACAACCTCCACCTCCGGGTTCAAGC T C SLC25A13 Ensembl:ENSG00000004864 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs897715361 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1692,RMVar_hsa_circ_83648,RMVar_hsa_circ_246715,RMVar_hsa_circ_267057 18491 RMVar_ID_18491 Human_SNP_ID_331702216 A-to-I Human chr7 + 96709741 96709741 96709741 ACTCGTCGTCTTCCTCTAACAGACCTAAGTCTACCGGCTGCTTTTTCTCTGACATCTCGACTGTC ACTCGTCGTCTTCCTCTAACAGACCTAAGTCTTCCGGCTGCTTTTTCTCTGACATCTCGACTGTC A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs774755484 Functional Loss SNV dbSNP153 33..33 33 - - - 18492 RMVar_ID_18492 Human_SNP_ID_331801473 A-to-I Human chr7 + 97130308 97130308 97130308 AAAAAAAAAAAACCTTGATGTAGAAAACATATATGTGTGACAAATCACCATTCAATAAACCATCA AAAAAAAAAAAACCTTGATGTAGAAAACATATGTGTGTGACAAATCACCATTCAATAAACCATCA A G SDHAF3 Ensembl:ENSG00000196636 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs887548317 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118295,RMVar_hsa_circ_246745 18493 RMVar_ID_18493 Human_SNP_ID_331806083 A-to-I Human chr7 + 97148021 97148021 97148021 TCACTCCCAGGTTCAAGCAATTCTCATACCTCAGCCTCCCAAGTAGCTGGGATTACAGGCACATG TCACTCCCAGGTTCAAGCAATTCTCATACCTCGGCCTCCCAAGTAGCTGGGATTACAGGCACATG A G SDHAF3 Ensembl:ENSG00000196636 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1236345868 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118295,RMVar_hsa_circ_246745 18494 RMVar_ID_18494 Human_SNP_ID_331978205 A-to-I Human chr7 - 97869093 97869093 97869093 ATGATTGCCTTTCTGTTCAGTGTCTGAGTGCTATGAAGATTGCACACAGAGGTCCAGATGCATTC ATGATTGCCTTTCTGTTCAGTGTCTGAGTGCTGTGAAGATTGCACACAGAGGTCCAGATGCATTC T C AC079781.5,ASNS Ensembl:ENSG00000284707,Ensembl:ENSG00000070669 lincRNA,Protein coding exon,CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs536609342 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1144377,Human_RBP_ID_1690017,Human_RBP_ID_2049738,Human_RBP_ID_3859017,Human_RBP_ID_4952772,Human_RBP_ID_5105385,Human_RBP_ID_5625152,Human_RBP_ID_8674869,Human_RBP_ID_17314678,Human_RBP_ID_18108069,Human_RBP_ID_18887750,Human_RBP_ID_22110943,Human_RBP_ID_22464588,Human_RBP_ID_22774691,Human_RBP_ID_23080098,Human_RBP_ID_24233303,Human_RBP_ID_24562958,Human_RBP_ID_26131111 Human_Splice_Rec_892980,Human_Splice_Rec_893006,Human_Splice_Rec_893030,Human_Splice_Rec_893052,Human_Splice_Rec_893094,Human_Splice_Rec_893138,Human_Splice_Rec_893172,Human_Splice_Rec_893180,Human_Splice_Rec_893184,Human_Splice_Rec_893192,Human_Splice_Rec_893198,Human_Splice_Rec_893202,Human_Splice_Rec_893216,Human_Splice_Rec_893250 RMVar_hsa_circ_48624,RMVar_hsa_circ_21947,RMVar_hsa_circ_57276,RMVar_hsa_circ_86071,RMVar_hsa_circ_246750,RMVar_hsa_circ_51772 18495 RMVar_ID_18495 Human_SNP_ID_331978444 A-to-I Human chr7 - 97870240 97870240 97870240 TCTCAAAACGGAATGTATCTGGACCTCTGTGTACAATCTTCGTAGCACTCAGACACTGAACAGAA TCTCAAAACGGAATGTATCTGGACCTCTGTGTGCAATCTTCGTAGCACTCAGACACTGAACAGAA T C AC079781.5,ASNS Ensembl:ENSG00000284707,Ensembl:ENSG00000070669 lincRNA,Protein coding intron,intron GSE100210;GSE107867 HepG2 cell line;ASD brains,cerebellum - 29129909,30559470 RNA-Seq:(High) rs551323113 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1690029,Human_RBP_ID_7775083,Human_RBP_ID_10368385,Human_RBP_ID_16259061,Human_RBP_ID_18887756 RMVar_hsa_circ_86071,RMVar_hsa_circ_246750 18496 RMVar_ID_18496 Human_SNP_ID_332003231 A-to-I Human chr7 - 97967909 97967886 97967910 CGGCTCACTGTAGCCTCTGCGTCCCAGGTTCAAGCCATTCTCCCGCCTCAGCTTCCCGAGTAGCT CGGCTCACTGTAGCCTCTGCGTCCCAGGTTC________________________CCGAGTAGCT GGAAGCTGAGGCGGGAGAATGGCTT G AC079781.5,AC004967.2 Ensembl:ENSG00000284707,Ensembl:ENSG00000285725 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277673759 Functional Loss DEL dbSNP153 32..55 33 - - - RMVar_hsa_circ_246753,RMVar_hsa_circ_122877,RMVar_hsa_circ_76647,RMVar_hsa_circ_246754 18497 RMVar_ID_18497 Human_SNP_ID_332003361 A-to-I Human chr7 - 97968431 97968431 97968431 TGATTGCGCCACTGCACTCTACCCTGGGCAACAGAGCGAGATTCCATCTCAAAAAAAAAAAAGGA TGATTGCGCCACTGCACTCTACCCTGGGCAACGGAGCGAGATTCCATCTCAAAAAAAAAAAAGGA T C AC079781.5,AC004967.2 Ensembl:ENSG00000284707,Ensembl:ENSG00000285725 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1217068032 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_246753,RMVar_hsa_circ_122877,RMVar_hsa_circ_76647,RMVar_hsa_circ_246754 18498 RMVar_ID_18498 Human_SNP_ID_332003384 A-to-I Human chr7 - 97968524 97968524 97968524 ATGTATCATGGTGCATGCCTGTAGTCCCAGCTACCTGGGAGGCTGAGGTGGGAGGATCGCTTGAG ATGTATCATGGTGCATGCCTGTAGTCCCAGCTTCCTGGGAGGCTGAGGTGGGAGGATCGCTTGAG T A AC079781.5,AC004967.2 Ensembl:ENSG00000284707,Ensembl:ENSG00000285725 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1164131155 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_246753,RMVar_hsa_circ_122877,RMVar_hsa_circ_76647,RMVar_hsa_circ_246754 18499 RMVar_ID_18499 Human_SNP_ID_332042218 A-to-I Human chr7 + 98115979 98115979 98115979 ACTGTCATGGTTTACTGCATCCCTGAACTCCTAGGCTCAAGCAGTCCTCCCATGTCAGCTCCTGA ACTGTCATGGTTTACTGCATCCCTGAACTCCTGGGCTCAAGCAGTCCTCCCATGTCAGCTCCTGA A G LMTK2 Ensembl:ENSG00000164715 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs980342081 Functional Loss SNV dbSNP153 33..33 33 - - - 18500 RMVar_ID_18500 Human_SNP_ID_332056676 A-to-I Human chr7 + 98173945 98173945 98173945 GGATGTGGTGACGGGTGCCTGTAGTCCCAGCTATTCGGGAGGCTGAGGCAGGAGAATGGCGTGAA GGATGTGGTGACGGGTGCCTGTAGTCCCAGCTGTTCGGGAGGCTGAGGCAGGAGAATGGCGTGAA A G LMTK2 Ensembl:ENSG00000164715 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs987989274 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112734,RMVar_hsa_circ_246755,RMVar_hsa_circ_77950,RMVar_hsa_circ_246761,RMVar_hsa_circ_35983,RMVar_hsa_circ_98598,RMVar_hsa_circ_246763,RMVar_hsa_circ_267331 18501 RMVar_ID_18501 Human_SNP_ID_332075207 A-to-I Human chr7 - 98239549 98239548 98239550 GGATTTCTTTTTTTTATTTTTTAATTTGAGACAGAGTCTCGTTCCGTCACCCAGGCTGGAATGCC GGATTTCTTTTTTTTATTTTTTAATTTGAGA__GAGTCTCGTTCCGTCACCCAGGCTGGAATGCC CTG C TECPR1 Ensembl:ENSG00000205356 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs530487687 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_60094,RMVar_hsa_circ_515,RMVar_hsa_circ_370245,RMVar_hsa_circ_246773,RMVar_hsa_circ_73829,RMVar_hsa_circ_246776 18502 RMVar_ID_18502 Human_SNP_ID_332075209 A-to-I Human chr7 - 98239549 98239549 98239549 GGATTTCTTTTTTTTATTTTTTAATTTGAGACAGAGTCTCGTTCCGTCACCCAGGCTGGAATGCC GGATTTCTTTTTTTTATTTTTTAATTTGAGACGGAGTCTCGTTCCGTCACCCAGGCTGGAATGCC T C TECPR1 Ensembl:ENSG00000205356 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1352820889 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_73829,RMVar_hsa_circ_246776 18503 RMVar_ID_18503 Human_SNP_ID_332077720 A-to-I Human chr7 - 98247894 98247894 98247894 TAGCGAGACCCCATCTCTACAAAAAAAATTTTAAAAATTAGCCAGGTACGGTGGCACATGCCTGT TAGCGAGACCCCATCTCTACAAAAAAAATTTTTAAAATTAGCCAGGTACGGTGGCACATGCCTGT T A TECPR1 Ensembl:ENSG00000205356 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs940386714 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60094 18504 RMVar_ID_18504 Human_SNP_ID_332077721 A-to-I Human chr7 - 98247894 98247894 98247894 TAGCGAGACCCCATCTCTACAAAAAAAATTTTAAAAATTAGCCAGGTACGGTGGCACATGCCTGT TAGCGAGACCCCATCTCTACAAAAAAAATTTTGAAAATTAGCCAGGTACGGTGGCACATGCCTGT T C TECPR1 Ensembl:ENSG00000205356 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs940386714 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60094 18505 RMVar_ID_18505 Human_SNP_ID_332079048 A-to-I Human chr7 - 98253579 98253579 98253579 CAAGCTAAAGTCAGGGTCAGACACAGGACTCCACAGAGCCATCCGGGGTGAACAAGAGGCTTCTG CAAGCTAAAGTCAGGGTCAGACACAGGACTCCGCAGAGCCATCCGGGGTGAACAAGAGGCTTCTG T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6972314 Functional Loss SNV dbSNP153 33..33 33 - - - 18506 RMVar_ID_18506 Human_SNP_ID_332080521 A-to-I Human chr7 + 98259457 98259457 98259457 GCCTGGCCAACATAGTGAAACCTGTCTCTACTAAAAAATACAAAATTAGCTGGGCATGGTGGTGC GCCTGGCCAACATAGTGAAACCTGTCTCTACTGAAAAATACAAAATTAGCTGGGCATGGTGGTGC A G BRI3 Ensembl:ENSG00000164713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1024537242 Functional Loss SNV dbSNP153 33..33 33 - - - 18507 RMVar_ID_18507 Human_SNP_ID_332116757 A-to-I Human chr7 - 98388782 98388782 98388782 TTTCATAGAGACAGGGTTTCACTATGCTGCCCAGGCTGGTCTTGAACTCCTGGGCTCAAGCCGTC TTTCATAGAGACAGGGTTTCACTATGCTGCCCGGGCTGGTCTTGAACTCCTGGGCTCAAGCCGTC T C BAIAP2L1 Ensembl:ENSG00000006453 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1243185389 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90201,RMVar_hsa_circ_246783,RMVar_hsa_circ_102476,RMVar_hsa_circ_246793 18508 RMVar_ID_18508 Human_SNP_ID_332252386 A-to-I Human chr7 + 98904010 98904010 98904010 TTTTTTATTTTTAGTAGAGATGGGATTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCT TTTTTTATTTTTAGTAGAGATGGGATTTCACCGTGTTGGCCAGGCTGGTCTCGAACTCCTGACCT A G TRRAP Ensembl:ENSG00000196367 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1289313311 Functional Loss SNV dbSNP153 33..33 33 - - - 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_246822,RMVar_hsa_circ_246823 18509 RMVar_ID_18509 Human_SNP_ID_332256180 A-to-I Human chr7 + 98917979 98917979 98917979 ACCCATCTCTACAAAAAATACAAAAATTAGCCAAGCATGGTGGCCGACACCTGTAATCCCAGCTA ACCCATCTCTACAAAAAATACAAAAATTAGCCCAGCATGGTGGCCGACACCTGTAATCCCAGCTA A C TRRAP Ensembl:ENSG00000196367 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs74964127 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66503,RMVar_hsa_circ_125590,RMVar_hsa_circ_80773,RMVar_hsa_circ_246796,RMVar_hsa_circ_10888,RMVar_hsa_circ_246800,RMVar_hsa_circ_95390,RMVar_hsa_circ_98787,RMVar_hsa_circ_246805,RMVar_hsa_circ_246806,RMVar_hsa_circ_112413,RMVar_hsa_circ_246808,RMVar_hsa_circ_97292,RMVar_hsa_circ_126943,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_246818,RMVar_hsa_circ_246823,RMVar_hsa_circ_109026,RMVar_hsa_circ_106098,RMVar_hsa_circ_246825,RMVar_hsa_circ_246826,RMVar_hsa_circ_372956,RMVar_hsa_circ_71857,RMVar_hsa_circ_246827,RMVar_hsa_circ_83393,RMVar_hsa_circ_126463,RMVar_hsa_circ_246828,RMVar_hsa_circ_125823,RMVar_hsa_circ_116768,RMVar_hsa_circ_40081,RMVar_hsa_circ_119702,RMVar_hsa_circ_246830,RMVar_hsa_circ_246831,RMVar_hsa_circ_246832,RMVar_hsa_circ_246834,RMVar_hsa_circ_80776,RMVar_hsa_circ_246835 18510 RMVar_ID_18510 Human_SNP_ID_332256304 A-to-I Human chr7 + 98918334 98918334 98918334 CTCACTGCAACCTCCGCCTCCCGGGTTCAAGCAATTCTTCTGTCTCAGCCTCCTGAGTAGCTGGG CTCACTGCAACCTCCGCCTCCCGGGTTCAAGCCATTCTTCTGTCTCAGCCTCCTGAGTAGCTGGG A C TRRAP Ensembl:ENSG00000196367 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs546139146 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66503,RMVar_hsa_circ_125590,RMVar_hsa_circ_80773,RMVar_hsa_circ_246796,RMVar_hsa_circ_10888,RMVar_hsa_circ_246800,RMVar_hsa_circ_95390,RMVar_hsa_circ_98787,RMVar_hsa_circ_246805,RMVar_hsa_circ_246806,RMVar_hsa_circ_112413,RMVar_hsa_circ_246808,RMVar_hsa_circ_97292,RMVar_hsa_circ_126943,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_246818,RMVar_hsa_circ_246823,RMVar_hsa_circ_109026,RMVar_hsa_circ_106098,RMVar_hsa_circ_246825,RMVar_hsa_circ_246826,RMVar_hsa_circ_372956,RMVar_hsa_circ_71857,RMVar_hsa_circ_246827,RMVar_hsa_circ_83393,RMVar_hsa_circ_126463,RMVar_hsa_circ_246828,RMVar_hsa_circ_125823,RMVar_hsa_circ_116768,RMVar_hsa_circ_40081,RMVar_hsa_circ_119702,RMVar_hsa_circ_246830,RMVar_hsa_circ_246831,RMVar_hsa_circ_246832,RMVar_hsa_circ_246834,RMVar_hsa_circ_80776,RMVar_hsa_circ_246835 18511 RMVar_ID_18511 Human_SNP_ID_332256315 A-to-I Human chr7 + 98918370 98918370 98918370 CTTCTGTCTCAGCCTCCTGAGTAGCTGGGACTACAGACGCGTACCACCATGCCTGGCTAATTTTT CTTCTGTCTCAGCCTCCTGAGTAGCTGGGACTGCAGACGCGTACCACCATGCCTGGCTAATTTTT A G TRRAP Ensembl:ENSG00000196367 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1554409896 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66503,RMVar_hsa_circ_125590,RMVar_hsa_circ_80773,RMVar_hsa_circ_246796,RMVar_hsa_circ_10888,RMVar_hsa_circ_246800,RMVar_hsa_circ_95390,RMVar_hsa_circ_98787,RMVar_hsa_circ_246805,RMVar_hsa_circ_246806,RMVar_hsa_circ_112413,RMVar_hsa_circ_246808,RMVar_hsa_circ_97292,RMVar_hsa_circ_126943,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_246818,RMVar_hsa_circ_246823,RMVar_hsa_circ_109026,RMVar_hsa_circ_106098,RMVar_hsa_circ_246825,RMVar_hsa_circ_246826,RMVar_hsa_circ_372956,RMVar_hsa_circ_71857,RMVar_hsa_circ_246827,RMVar_hsa_circ_83393,RMVar_hsa_circ_126463,RMVar_hsa_circ_246828,RMVar_hsa_circ_125823,RMVar_hsa_circ_116768,RMVar_hsa_circ_40081,RMVar_hsa_circ_119702,RMVar_hsa_circ_246830,RMVar_hsa_circ_246831,RMVar_hsa_circ_246832,RMVar_hsa_circ_246834,RMVar_hsa_circ_80776,RMVar_hsa_circ_246835 18512 RMVar_ID_18512 Human_SNP_ID_332256415 A-to-I Human chr7 + 98918792 98918792 98918792 AAAGTTCATATGTTGGCCAGGCACTGTGGCTCACGCCTGTAATCCCAGCACTATGGGAGGCTGAG AAAGTTCATATGTTGGCCAGGCACTGTGGCTCCCGCCTGTAATCCCAGCACTATGGGAGGCTGAG A C TRRAP Ensembl:ENSG00000196367 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1239860276 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66503,RMVar_hsa_circ_125590,RMVar_hsa_circ_80773,RMVar_hsa_circ_246796,RMVar_hsa_circ_10888,RMVar_hsa_circ_246800,RMVar_hsa_circ_95390,RMVar_hsa_circ_98787,RMVar_hsa_circ_246805,RMVar_hsa_circ_246806,RMVar_hsa_circ_112413,RMVar_hsa_circ_246808,RMVar_hsa_circ_97292,RMVar_hsa_circ_126943,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_246818,RMVar_hsa_circ_246823,RMVar_hsa_circ_109026,RMVar_hsa_circ_106098,RMVar_hsa_circ_246825,RMVar_hsa_circ_246826,RMVar_hsa_circ_372956,RMVar_hsa_circ_71857,RMVar_hsa_circ_246827,RMVar_hsa_circ_83393,RMVar_hsa_circ_126463,RMVar_hsa_circ_246828,RMVar_hsa_circ_125823,RMVar_hsa_circ_116768,RMVar_hsa_circ_40081,RMVar_hsa_circ_119702,RMVar_hsa_circ_246830,RMVar_hsa_circ_246831,RMVar_hsa_circ_246832,RMVar_hsa_circ_246834,RMVar_hsa_circ_80776,RMVar_hsa_circ_246835 18513 RMVar_ID_18513 Human_SNP_ID_332256992 A-to-I Human chr7 + 98920979 98920979 98920979 CTTCTGCCTCAGCCTCCCCAGTAGCTGGGATTACAGGCATGTGCCACCACGCCCAGCTAATTTTG CTTCTGCCTCAGCCTCCCCAGTAGCTGGGATTGCAGGCATGTGCCACCACGCCCAGCTAATTTTG A G TRRAP Ensembl:ENSG00000196367 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs567255083 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66503,RMVar_hsa_circ_125590,RMVar_hsa_circ_80773,RMVar_hsa_circ_246796,RMVar_hsa_circ_10888,RMVar_hsa_circ_246800,RMVar_hsa_circ_95390,RMVar_hsa_circ_98787,RMVar_hsa_circ_246805,RMVar_hsa_circ_246806,RMVar_hsa_circ_112413,RMVar_hsa_circ_246808,RMVar_hsa_circ_97292,RMVar_hsa_circ_126943,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_246818,RMVar_hsa_circ_246823,RMVar_hsa_circ_109026,RMVar_hsa_circ_106098,RMVar_hsa_circ_246825,RMVar_hsa_circ_246826,RMVar_hsa_circ_372956,RMVar_hsa_circ_71857,RMVar_hsa_circ_246827,RMVar_hsa_circ_83393,RMVar_hsa_circ_126463,RMVar_hsa_circ_246828,RMVar_hsa_circ_125823,RMVar_hsa_circ_116768,RMVar_hsa_circ_40081,RMVar_hsa_circ_119702,RMVar_hsa_circ_246830,RMVar_hsa_circ_246831,RMVar_hsa_circ_246832,RMVar_hsa_circ_246834,RMVar_hsa_circ_80776,RMVar_hsa_circ_246835 18514 RMVar_ID_18514 Human_SNP_ID_332283192 A-to-I Human chr7 + 99017428 99017428 99017428 ACCTCAGGTGATCCACCCGCCTTGGCCTCCCAAAGTGCCGGGATTGCAGGCGTGAGCCACTGCGC ACCTCAGGTGATCCACCCGCCTTGGCCTCCCAGAGTGCCGGGATTGCAGGCGTGAGCCACTGCGC A G TRRAP Ensembl:ENSG00000196367 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251554112 Functional Loss SNV dbSNP153 33..33 33 - - - 18515 RMVar_ID_18515 Human_SNP_ID_332294432 A-to-I Human chr7 - 99057736 99057736 99057736 AAAATTAGCCAGGCATGGTGATGCACGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTAGCCAGGCATGGTGATGCACGCCTGTGGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA T C SMURF1 Ensembl:ENSG00000198742 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1036309141 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_246897,RMVar_hsa_circ_86929,RMVar_hsa_circ_266185,RMVar_hsa_circ_123383,RMVar_hsa_circ_246907,RMVar_hsa_circ_378970,RMVar_hsa_circ_294863,RMVar_hsa_circ_246908,RMVar_hsa_circ_19467,RMVar_hsa_circ_278507,RMVar_hsa_circ_363661 18516 RMVar_ID_18516 Human_SNP_ID_332296632 A-to-I Human chr7 + 99065273 99065273 99065273 AACACCAGCACACTTGGATAATTTTTTTGTAGAAACGGGGTCTCAGTATGTTGCCCAGGCGGGTC AACACCAGCACACTTGGATAATTTTTTTGTAGCAACGGGGTCTCAGTATGTTGCCCAGGCGGGTC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs748794107 Functional Loss SNV dbSNP153 33..33 33 - - - 18517 RMVar_ID_18517 Human_SNP_ID_332310832 A-to-I Human chr7 - 99129529 99129529 99129529 AAAATTAGCTGGGCATAGTGGTGCACACCTGTAGTCCCAGCTACTTGGGAGCTGAGGTGGGAGAA AAAATTAGCTGGGCATAGTGGTGCACACCTGTCGTCCCAGCTACTTGGGAGCTGAGGTGGGAGAA T G SMURF1 Ensembl:ENSG00000198742 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs368472445 Functional Loss SNV dbSNP153 33..33 33 - - - 18518 RMVar_ID_18518 Human_SNP_ID_332363614 A-to-I Human chr7 + 99333163 99333163 99333163 GTGATCCACCTGCCTTGGCCTCCCAAAGTGCTAGTATTACAAGCGTGAGCCACCGTGCCTGGCCA GTGATCCACCTGCCTTGGCCTCCCAAAGTGCTGGTATTACAAGCGTGAGCCACCGTGCCTGGCCA A G AC004922.1,ARPC1A Ensembl:ENSG00000284292,Ensembl:ENSG00000241685 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1434868375 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82257,RMVar_hsa_circ_246914 18519 RMVar_ID_18519 Human_SNP_ID_332365173 A-to-I Human chr7 + 99339270 99339270 99339270 CATACATACATATTCATAAACAAGCTTAGGCCAAGCACAGTGGCTTACACCTGTAATCCCAGCAC CATACATACATATTCATAAACAAGCTTAGGCCGAGCACAGTGGCTTACACCTGTAATCCCAGCAC A G AC004922.1,ARPC1A Ensembl:ENSG00000284292,Ensembl:ENSG00000241685 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1210848464 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15222,RMVar_hsa_circ_290462,RMVar_hsa_circ_312112,RMVar_hsa_circ_374284,RMVar_hsa_circ_291744,RMVar_hsa_circ_90807,RMVar_hsa_circ_89831,RMVar_hsa_circ_98173,RMVar_hsa_circ_246916,RMVar_hsa_circ_246918,RMVar_hsa_circ_246919,RMVar_hsa_circ_246920,RMVar_hsa_circ_246917,RMVar_hsa_circ_345008,RMVar_hsa_circ_363999,RMVar_hsa_circ_315932,RMVar_hsa_circ_246922,RMVar_hsa_circ_19323,RMVar_hsa_circ_246921 18520 RMVar_ID_18520 Human_SNP_ID_332365393 A-to-I Human chr7 + 99340302 99340302 99340302 CTCCCGCCTCAGCCTCCCGAGTTGCTGGGATTACAGGTGCCTGCCACAATGCCCAGCTAATTTTT CTCCCGCCTCAGCCTCCCGAGTTGCTGGGATTCCAGGTGCCTGCCACAATGCCCAGCTAATTTTT A C AC004922.1,ARPC1A Ensembl:ENSG00000284292,Ensembl:ENSG00000241685 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1320641303 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15222,RMVar_hsa_circ_290462,RMVar_hsa_circ_312112,RMVar_hsa_circ_374284,RMVar_hsa_circ_291744,RMVar_hsa_circ_90807,RMVar_hsa_circ_89831,RMVar_hsa_circ_98173,RMVar_hsa_circ_246916,RMVar_hsa_circ_246918,RMVar_hsa_circ_246919,RMVar_hsa_circ_246920,RMVar_hsa_circ_246917,RMVar_hsa_circ_345008,RMVar_hsa_circ_315932,RMVar_hsa_circ_55242,RMVar_hsa_circ_246922,RMVar_hsa_circ_19323,RMVar_hsa_circ_246921 18521 RMVar_ID_18521 Human_SNP_ID_332365404 A-to-I Human chr7 + 99340346 99340346 99340346 CACAATGCCCAGCTAATTTTTGTATTTTTAGTAGATGTGGGATTTCACCACATTGGACAGGCTGG CACAATGCCCAGCTAATTTTTGTATTTTTAGTGGATGTGGGATTTCACCACATTGGACAGGCTGG A G AC004922.1,ARPC1A Ensembl:ENSG00000284292,Ensembl:ENSG00000241685 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1396117720 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15222,RMVar_hsa_circ_290462,RMVar_hsa_circ_312112,RMVar_hsa_circ_374284,RMVar_hsa_circ_291744,RMVar_hsa_circ_90807,RMVar_hsa_circ_89831,RMVar_hsa_circ_98173,RMVar_hsa_circ_246916,RMVar_hsa_circ_246918,RMVar_hsa_circ_246919,RMVar_hsa_circ_246920,RMVar_hsa_circ_246917,RMVar_hsa_circ_345008,RMVar_hsa_circ_315932,RMVar_hsa_circ_55242,RMVar_hsa_circ_246922,RMVar_hsa_circ_19323,RMVar_hsa_circ_246921 18522 RMVar_ID_18522 Human_SNP_ID_332365469 A-to-I Human chr7 + 99340582 99340582 99340582 CTCCCATCTCAGCCTCCCCAGGAGCTGGTACTAAAGGTGTGCGCCAGCACACCCGGCTAATTTTT CTCCCATCTCAGCCTCCCCAGGAGCTGGTACTGAAGGTGTGCGCCAGCACACCCGGCTAATTTTT A G AC004922.1,ARPC1A Ensembl:ENSG00000284292,Ensembl:ENSG00000241685 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs966785520 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15222,RMVar_hsa_circ_290462,RMVar_hsa_circ_312112,RMVar_hsa_circ_374284,RMVar_hsa_circ_291744,RMVar_hsa_circ_90807,RMVar_hsa_circ_89831,RMVar_hsa_circ_98173,RMVar_hsa_circ_246916,RMVar_hsa_circ_246918,RMVar_hsa_circ_246919,RMVar_hsa_circ_246920,RMVar_hsa_circ_246917,RMVar_hsa_circ_345008,RMVar_hsa_circ_315932,RMVar_hsa_circ_55242,RMVar_hsa_circ_246922,RMVar_hsa_circ_19323,RMVar_hsa_circ_246921 18523 RMVar_ID_18523 Human_SNP_ID_332365997 A-to-I Human chr7 + 99342848 99342848 99342848 GGGTTCACACCATTCTCCTGCCTCAGCCTCCTAAGTAGCTGGGACTACACGCGCCTGTCACCACG GGGTTCACACCATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACACGCGCCTGTCACCACG A G AC004922.1,ARPC1A Ensembl:ENSG00000284292,Ensembl:ENSG00000241685 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs55672337 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15222,RMVar_hsa_circ_290462,RMVar_hsa_circ_312112,RMVar_hsa_circ_374284,RMVar_hsa_circ_291744,RMVar_hsa_circ_90807,RMVar_hsa_circ_89831,RMVar_hsa_circ_98173,RMVar_hsa_circ_246916,RMVar_hsa_circ_246918,RMVar_hsa_circ_246919,RMVar_hsa_circ_246920,RMVar_hsa_circ_246917,RMVar_hsa_circ_345008,RMVar_hsa_circ_315932,RMVar_hsa_circ_55242,RMVar_hsa_circ_246922,RMVar_hsa_circ_19323,RMVar_hsa_circ_246921 18524 RMVar_ID_18524 Human_SNP_ID_332365999 A-to-I Human chr7 + 99342852 99342852 99342852 TCACACCATTCTCCTGCCTCAGCCTCCTAAGTAGCTGGGACTACACGCGCCTGTCACCACGCCCG TCACACCATTCTCCTGCCTCAGCCTCCTAAGTCGCTGGGACTACACGCGCCTGTCACCACGCCCG A C AC004922.1,ARPC1A Ensembl:ENSG00000284292,Ensembl:ENSG00000241685 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs964230778 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15222,RMVar_hsa_circ_290462,RMVar_hsa_circ_312112,RMVar_hsa_circ_374284,RMVar_hsa_circ_291744,RMVar_hsa_circ_90807,RMVar_hsa_circ_89831,RMVar_hsa_circ_98173,RMVar_hsa_circ_246916,RMVar_hsa_circ_246918,RMVar_hsa_circ_246919,RMVar_hsa_circ_246920,RMVar_hsa_circ_246917,RMVar_hsa_circ_345008,RMVar_hsa_circ_315932,RMVar_hsa_circ_55242,RMVar_hsa_circ_246922,RMVar_hsa_circ_19323,RMVar_hsa_circ_246921 18525 RMVar_ID_18525 Human_SNP_ID_332366645 A-to-I Human chr7 + 99345115 99345115 99345115 TGCCATCGTGCCCGGCTAATTTTTGTAGTTTTAGTAGAGACAAGGTTTCACCATCTTGGCCAGGC TGCCATCGTGCCCGGCTAATTTTTGTAGTTTTGGTAGAGACAAGGTTTCACCATCTTGGCCAGGC A G AC004922.1,ARPC1A Ensembl:ENSG00000284292,Ensembl:ENSG00000241685 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1241960801 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16264976 RMVar_hsa_circ_15222,RMVar_hsa_circ_312112,RMVar_hsa_circ_374284,RMVar_hsa_circ_291744,RMVar_hsa_circ_90807,RMVar_hsa_circ_89831,RMVar_hsa_circ_28226,RMVar_hsa_circ_98173,RMVar_hsa_circ_246918,RMVar_hsa_circ_246919,RMVar_hsa_circ_246920,RMVar_hsa_circ_246917,RMVar_hsa_circ_315932,RMVar_hsa_circ_55242,RMVar_hsa_circ_246922,RMVar_hsa_circ_19323,RMVar_hsa_circ_246921,RMVar_hsa_circ_296143,RMVar_hsa_circ_345050,RMVar_hsa_circ_88419,RMVar_hsa_circ_246923,RMVar_hsa_circ_246925,RMVar_hsa_circ_246924 18526 RMVar_ID_18526 Human_SNP_ID_332369570 A-to-I Human chr7 + 99357433 99357433 99357433 GGCTGGAACTCCTGAGCTCAAGTTCTCCTCCCACCTCAGCCTCTCAAGCAGCTGGAGCCACAGAC GGCTGGAACTCCTGAGCTCAAGTTCTCCTCCCCCCTCAGCCTCTCAAGCAGCTGGAGCCACAGAC A C AC004922.1,ARPC1A Ensembl:ENSG00000284292,Ensembl:ENSG00000241685 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs987077682 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15222,RMVar_hsa_circ_374284,RMVar_hsa_circ_90807,RMVar_hsa_circ_89831,RMVar_hsa_circ_28226,RMVar_hsa_circ_98173,RMVar_hsa_circ_246918,RMVar_hsa_circ_246919,RMVar_hsa_circ_246920,RMVar_hsa_circ_246922,RMVar_hsa_circ_345050,RMVar_hsa_circ_88419,RMVar_hsa_circ_40794,RMVar_hsa_circ_246923,RMVar_hsa_circ_246924,RMVar_hsa_circ_112700,RMVar_hsa_circ_246926,RMVar_hsa_circ_343932 18527 RMVar_ID_18527 Human_SNP_ID_332369571 A-to-I Human chr7 + 99357433 99357433 99357433 GGCTGGAACTCCTGAGCTCAAGTTCTCCTCCCACCTCAGCCTCTCAAGCAGCTGGAGCCACAGAC GGCTGGAACTCCTGAGCTCAAGTTCTCCTCCCTCCTCAGCCTCTCAAGCAGCTGGAGCCACAGAC A T AC004922.1,ARPC1A Ensembl:ENSG00000284292,Ensembl:ENSG00000241685 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs987077682 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15222,RMVar_hsa_circ_374284,RMVar_hsa_circ_90807,RMVar_hsa_circ_89831,RMVar_hsa_circ_28226,RMVar_hsa_circ_98173,RMVar_hsa_circ_246918,RMVar_hsa_circ_246919,RMVar_hsa_circ_246920,RMVar_hsa_circ_246922,RMVar_hsa_circ_345050,RMVar_hsa_circ_88419,RMVar_hsa_circ_40794,RMVar_hsa_circ_246923,RMVar_hsa_circ_246924,RMVar_hsa_circ_112700,RMVar_hsa_circ_246926,RMVar_hsa_circ_343932 18528 RMVar_ID_18528 Human_SNP_ID_332369930 A-to-I Human chr7 + 99358714 99358714 99358714 AGGCATGCGCCACCATACCTGGCTAATTTTGTATTTTTAGAAGAGACGGGGTTTCTCCATGTTGG AGGCATGCGCCACCATACCTGGCTAATTTTGTGTTTTTAGAAGAGACGGGGTTTCTCCATGTTGG A G AC004922.1,ARPC1A Ensembl:ENSG00000284292,Ensembl:ENSG00000241685 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1467516441 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_894821 RMVar_hsa_circ_15222,RMVar_hsa_circ_374284,RMVar_hsa_circ_90807,RMVar_hsa_circ_28226,RMVar_hsa_circ_98173,RMVar_hsa_circ_246919,RMVar_hsa_circ_246920,RMVar_hsa_circ_246922,RMVar_hsa_circ_345050,RMVar_hsa_circ_88419,RMVar_hsa_circ_40794,RMVar_hsa_circ_246923,RMVar_hsa_circ_246924,RMVar_hsa_circ_112700,RMVar_hsa_circ_246926,RMVar_hsa_circ_343932,RMVar_hsa_circ_246928,RMVar_hsa_circ_301379,RMVar_hsa_circ_327479,RMVar_hsa_circ_246927 18529 RMVar_ID_18529 Human_SNP_ID_332371097 A-to-I Human chr7 + 99362862 99362862 99362862 ACAAGTTGTTTCATTTATCTGTTCCCCTGCTTAGCTTGGTCGGAATCTAGTGGTGTGTCTGCTGC ACAAGTTGTTTCATTTATCTGTTCCCCTGCTTGGCTTGGTCGGAATCTAGTGGTGTGTCTGCTGC A G AC004922.1,ARPC1A Ensembl:ENSG00000284292,Ensembl:ENSG00000241685 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7804854 Functional Loss SNV dbSNP153 33..33 33 - - - 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 18530 RMVar_ID_18530 Human_SNP_ID_332371281 A-to-I Human chr7 + 99363778 99363778 99363778 CTCACTGCAGCCACCAACTCCTTGCCTCCAGCAGCCCTCCCACCTCAGCCTCCCAAGCTGCTGGG CTCACTGCAGCCACCAACTCCTTGCCTCCAGCGGCCCTCCCACCTCAGCCTCCCAAGCTGCTGGG A G AC004922.1,ARPC1A Ensembl:ENSG00000284292,Ensembl:ENSG00000241685 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886715440 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90807,RMVar_hsa_circ_98173,RMVar_hsa_circ_246920,RMVar_hsa_circ_246922,RMVar_hsa_circ_88419,RMVar_hsa_circ_246923 18531 RMVar_ID_18531 Human_SNP_ID_332371476 A-to-I Human chr7 + 99364500 99364500 99364500 CTCCACGTTGGACATGCTGGTCTCGAACTCCCAACCTCAGGTGATCCACCCGCCTCAGCCTCCCC CTCCACGTTGGACATGCTGGTCTCGAACTCCCGACCTCAGGTGATCCACCCGCCTCAGCCTCCCC A G AC004922.1,ARPC1A Ensembl:ENSG00000284292,Ensembl:ENSG00000241685 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs777074538 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90807,RMVar_hsa_circ_98173,RMVar_hsa_circ_246920,RMVar_hsa_circ_246922,RMVar_hsa_circ_88419,RMVar_hsa_circ_246923 18532 RMVar_ID_18532 Human_SNP_ID_332371662 A-to-I Human chr7 + 99365268 99365267 99365269 AGGCCAGGAGTTTTGAGACCAGTTTGGGCAACATAGCGTGACCCCATCTCTATAAAAAAGCCAGG AGGCCAGGAGTTTTGAGACCAGTTTGGGCAAC__AGCGTGACCCCATCTCTATAAAAAAGCCAGG CAT C AC004922.1,ARPC1A Ensembl:ENSG00000284292,Ensembl:ENSG00000241685 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1554346259 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_90807,RMVar_hsa_circ_98173,RMVar_hsa_circ_246920,RMVar_hsa_circ_246922,RMVar_hsa_circ_88419,RMVar_hsa_circ_246923 18533 RMVar_ID_18533 Human_SNP_ID_332371664 A-to-I Human chr7 + 99365268 99365268 99365268 AGGCCAGGAGTTTTGAGACCAGTTTGGGCAACATAGCGTGACCCCATCTCTATAAAAAAGCCAGG AGGCCAGGAGTTTTGAGACCAGTTTGGGCAACGTAGCGTGACCCCATCTCTATAAAAAAGCCAGG A G AC004922.1,ARPC1A Ensembl:ENSG00000284292,Ensembl:ENSG00000241685 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs961776365 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90807,RMVar_hsa_circ_98173,RMVar_hsa_circ_246920,RMVar_hsa_circ_246922,RMVar_hsa_circ_88419,RMVar_hsa_circ_246923 18534 RMVar_ID_18534 Human_SNP_ID_332371665 A-to-I Human chr7 + 99365268 99365268 99365268 AGGCCAGGAGTTTTGAGACCAGTTTGGGCAACATAGCGTGACCCCATCTCTATAAAAAAGCCAGG AGGCCAGGAGTTTTGAGACCAGTTTGGGCAACTTAGCGTGACCCCATCTCTATAAAAAAGCCAGG A T AC004922.1,ARPC1A Ensembl:ENSG00000284292,Ensembl:ENSG00000241685 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs961776365 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90807,RMVar_hsa_circ_98173,RMVar_hsa_circ_246920,RMVar_hsa_circ_246922,RMVar_hsa_circ_88419,RMVar_hsa_circ_246923 18535 RMVar_ID_18535 Human_SNP_ID_332373525 A-to-I Human chr7 - 99372469 99372469 99372469 CCTCTTTTACCCAGGCTGGAATGTAGTGACGCAATCACAGCTCACTGAAGCCTCCAGCTCCTGGG CCTCTTTTACCCAGGCTGGAATGTAGTGACGCGATCACAGCTCACTGAAGCCTCCAGCTCCTGGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs918038924 Functional Loss SNV dbSNP153 33..33 33 - - - 18536 RMVar_ID_18536 Human_SNP_ID_332374725 A-to-I Human chr7 + 99376615 99376615 99376615 CAAACAGGCTGGGCGCGGTGGCTCACGCCTGTAATTCCAGCACTTTGGGAGGCCGAGGCAGGCAG CAAACAGGCTGGGCGCGGTGGCTCACGCCTGTGATTCCAGCACTTTGGGAGGCCGAGGCAGGCAG A G AC004922.1,ARPC1B Ensembl:ENSG00000284292,Ensembl:ENSG00000130429 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1255936055 Functional Loss SNV dbSNP153 33..33 33 - - - 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 18537 RMVar_ID_18537 Human_SNP_ID_332374730 A-to-I Human chr7 + 99376646 99376646 99376646 TAATTCCAGCACTTTGGGAGGCCGAGGCAGGCAGATTACCTGAGGTCGGGAGTTCGAGACCAGCC TAATTCCAGCACTTTGGGAGGCCGAGGCAGGCGGATTACCTGAGGTCGGGAGTTCGAGACCAGCC A G AC004922.1,ARPC1B Ensembl:ENSG00000284292,Ensembl:ENSG00000130429 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1413684667 Functional Loss SNV dbSNP153 33..33 33 - - - 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 18538 RMVar_ID_18538 Human_SNP_ID_332375116 A-to-I Human chr7 + 99377867 99377867 99377867 GTTGGGCAGGCTGGTCTCAAACTCCTGACCTCAGGTGATCCACCTGCCTCCGCCTCCCAAAGTCT GTTGGGCAGGCTGGTCTCAAACTCCTGACCTCCGGTGATCCACCTGCCTCCGCCTCCCAAAGTCT A C AC004922.1,ARPC1B Ensembl:ENSG00000284292,Ensembl:ENSG00000130429 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1440197264 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2475112,Human_miRNA_ID_2960898 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 18539 RMVar_ID_18539 Human_SNP_ID_332376454 A-to-I Human chr7 + 99382676 99382676 99382676 TTAAATTTTTTGTAGAGATAGGGTCTCACTGTATCGCCCATGCTTGTCTTGAACTTCTGGCCTGA TTAAATTTTTTGTAGAGATAGGGTCTCACTGTGTCGCCCATGCTTGTCTTGAACTTCTGGCCTGA A G AC004922.1,ARPC1B Ensembl:ENSG00000284292,Ensembl:ENSG00000130429 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474967592 Functional Loss SNV dbSNP153 33..33 33 - - - 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 18540 RMVar_ID_18540 Human_SNP_ID_332376915 A-to-I Human chr7 + 99384441 99384438 99384442 AGACCCCCCTCTCTACAAACAAATCAAAAATTAGTTGGGCACAGTGGCACATGCTTGTAATCCCA AGACCCCCCTCTCTACAAACAAATCAAAAA____TTGGGCACAGTGGCACATGCTTGTAATCCCA ATTAG A AC004922.1,ARPC1B Ensembl:ENSG00000284292,Ensembl:ENSG00000130429 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1436256499 Functional Loss DEL dbSNP153 31..34 33 - - - 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 18541 RMVar_ID_18541 Human_SNP_ID_332382357 A-to-I Human chr7 - 99402420 99402420 99402420 TAAATTTTTTGTAGAGATAGGGATCTCACTATATTGCCCAGGTGGTCTCCAACTCCTGGGCTCAA TAAATTTTTTGTAGAGATAGGGATCTCACTATGTTGCCCAGGTGGTCTCCAACTCCTGGGCTCAA T C PDAP1 Ensembl:ENSG00000106244 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027394721 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_354157,RMVar_hsa_circ_64753,RMVar_hsa_circ_331679 18542 RMVar_ID_18542 Human_SNP_ID_332382464 A-to-I Human chr7 - 99402770 99402770 99402770 GGTTCAAGCGCTTCTGCCCCAGCCTCCTGAGTAGCTGGGACTACAGGCGCCTGCCACCACGCCGG GGTTCAAGCGCTTCTGCCCCAGCCTCCTGAGTGGCTGGGACTACAGGCGCCTGCCACCACGCCGG T C PDAP1 Ensembl:ENSG00000106244 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1028406976 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_354157,RMVar_hsa_circ_64753,RMVar_hsa_circ_331679 18543 RMVar_ID_18543 Human_SNP_ID_332383250 A-to-I Human chr7 - 99405563 99405563 99405563 GGTCAAGAGATCAAGACCATTCTAGCCAACCAACATGGTTAAACCCCATCTCTACTAAAAATAAA GGTCAAGAGATCAAGACCATTCTAGCCAACCAGCATGGTTAAACCCCATCTCTACTAAAAATAAA T C PDAP1 Ensembl:ENSG00000106244 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1470484100 Functional Loss SNV dbSNP153 33..33 33 - - - 18544 RMVar_ID_18544 Human_SNP_ID_332395979 A-to-I Human chr7 + 99446677 99446666 99446677 TCACCCAGGCTGGAGTGCAGTGGCACAGTCATAGCTGACTGCAAGCTTGACCTCCTGGGCCCAAG TCACCCAGGCTGGAGTGCAGTG___________GCTGACTGCAAGCTTGACCTCCTGGGCCCAAG GGCACAGTCATA G CPSF4 Ensembl:ENSG00000160917 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1418459451 Functional Loss DEL dbSNP153 23..33 33 - - - Human_RBP_ID_16266150 RMVar_hsa_circ_327708 18545 RMVar_ID_18545 Human_SNP_ID_332400128 A-to-I Human chr7 - 99461822 99461822 99461822 GAAACCCTGTCTCTACTAAAAATACAAAAATTAGCTGGGTGTCGTGGCGCATGCCTGTAGTCCCA GAAACCCTGTCTCTACTAAAAATACAAAAATTGGCTGGGTGTCGTGGCGCATGCCTGTAGTCCCA T C PTCD1,ATP5MF-PTCD1,ATP5MF Ensembl:ENSG00000106246,Ensembl:ENSG00000248919,Ensembl:ENSG00000241468 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs964728796 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_176668 18546 RMVar_ID_18546 Human_SNP_ID_332400616 A-to-I Human chr7 - 99463700 99463700 99463700 ACGATCTCAGCTCAGTGCAACCTCCACCTCCCAGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCA ACGATCTCAGCTCAGTGCAACCTCCACCTCCCGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCA T C PTCD1,ATP5MF-PTCD1,ATP5MF Ensembl:ENSG00000106246,Ensembl:ENSG00000248919,Ensembl:ENSG00000241468 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1451154886 Functional Loss SNV dbSNP153 33..33 33 - - - 18547 RMVar_ID_18547 Human_SNP_ID_332403469 A-to-I Human chr7 + 99473640 99473640 99473640 GAAATAAGGAATTGTTGTTGCTGTTGTGTTTGAGACGAAGTGTTACTCTGTTGCCCAGTTTGGAG GAAATAAGGAATTGTTGTTGCTGTTGTGTTTGTGACGAAGTGTTACTCTGTTGCCCAGTTTGGAG A T ZNF789 Ensembl:ENSG00000198556 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1225976112 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2050125,Human_RBP_ID_16266751 18548 RMVar_ID_18548 Human_SNP_ID_332404408 A-to-I Human chr7 + 99477453 99477453 99477453 CCTTGACCTTCCCAGGCTCAGGTGATCCTCCCACCTCAGCCTCCCAAGTAGTTGGGACCACAGGT CCTTGACCTTCCCAGGCTCAGGTGATCCTCCCGCCTCAGCCTCCCAAGTAGTTGGGACCACAGGT A G ZNF789 Ensembl:ENSG00000198556 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1162971900 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40690,RMVar_hsa_circ_310856,RMVar_hsa_circ_246957 18549 RMVar_ID_18549 Human_SNP_ID_332404424 A-to-I Human chr7 + 99477529 99477529 99477529 CGCCTGGTTACTTTTGTATTTTTTGTAGAGACAGGGTTACACCATGTTGCCCAGGTTGTTCTTGA CGCCTGGTTACTTTTGTATTTTTTGTAGAGACCGGGTTACACCATGTTGCCCAGGTTGTTCTTGA A C ZNF789 Ensembl:ENSG00000198556 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs972761557 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16266874,Human_RBP_ID_22483549 RMVar_hsa_circ_40690,RMVar_hsa_circ_310856,RMVar_hsa_circ_246957 18550 RMVar_ID_18550 Human_SNP_ID_332404455 A-to-I Human chr7 + 99477674 99477674 99477674 AAGAGACTGAGTTTGAAAGAAAGGAGAGGACCAGTGGCTCATGCCTGGAATCCCAGCACTTTGGG AAGAGACTGAGTTTGAAAGAAAGGAGAGGACCGGTGGCTCATGCCTGGAATCCCAGCACTTTGGG A G ZNF789 Ensembl:ENSG00000198556 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560260561 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16266880 RMVar_hsa_circ_40690,RMVar_hsa_circ_310856,RMVar_hsa_circ_246957 18551 RMVar_ID_18551 Human_SNP_ID_332404483 A-to-I Human chr7 + 99477777 99477777 99477777 AGACCAGCCTGGCCAACATATAGTGAAACTCCATCTCTACTAAAAATACAAAAATTAGCTGGGTA AGACCAGCCTGGCCAACATATAGTGAAACTCCGTCTCTACTAAAAATACAAAAATTAGCTGGGTA A G ZNF789 Ensembl:ENSG00000198556 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1276722473 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40690,RMVar_hsa_circ_310856,RMVar_hsa_circ_246957 18552 RMVar_ID_18552 Human_SNP_ID_332404501 A-to-I Human chr7 + 99477873 99477873 99477873 GGGAAGCTGAGGCAGGAGAATTGCTTGAACCGAGGAGGTGGAGGTTGCAGTGAGCCGAGATCGCG GGGAAGCTGAGGCAGGAGAATTGCTTGAACCGCGGAGGTGGAGGTTGCAGTGAGCCGAGATCGCG A C ZNF789 Ensembl:ENSG00000198556 Protein coding intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs995976421 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40690,RMVar_hsa_circ_310856,RMVar_hsa_circ_246957 18553 RMVar_ID_18553 Human_SNP_ID_332405342 A-to-I Human chr7 + 99481709 99481709 99481709 AAACTCCCGATCTCGGGTGACCCGCCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG AAACTCCCGATCTCGGGTGACCCGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG A G ZNF789 Ensembl:ENSG00000198556 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1311705188 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40690,RMVar_hsa_circ_19923 18554 RMVar_ID_18554 Human_SNP_ID_332405556 A-to-I Human chr7 + 99482707 99482707 99482707 AGAAACCCTGTCTCTACTAAAAATTCAAAATTAGTCAGGCGTGGTGGCACATGCCTGTAATCTCA AGAAACCCTGTCTCTACTAAAAATTCAAAATTGGTCAGGCGTGGTGGCACATGCCTGTAATCTCA A G ZNF789 Ensembl:ENSG00000198556 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs953295628 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40690,RMVar_hsa_circ_19923 18555 RMVar_ID_18555 Human_SNP_ID_332405760 A-to-I Human chr7 + 99483537 99483537 99483537 CCTGTAGTTCCAGCTACTTGGGAGGCTGAGGCAGAAGAATTACTTGATCCTGGGAGGCAGAGGTT CCTGTAGTTCCAGCTACTTGGGAGGCTGAGGCCGAAGAATTACTTGATCCTGGGAGGCAGAGGTT A C ZNF789 Ensembl:ENSG00000198556 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1460397954 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5221647 RMVar_hsa_circ_40690,RMVar_hsa_circ_19923 18556 RMVar_ID_18556 Human_SNP_ID_332410059 A-to-I Human chr7 - 99497777 99497777 99497777 GCTCACTGCAACTTCTGCCTCCCAAGCCAAGCAATTCTCCTGCCTCTGTCTCCCGAGGAGCTGGA GCTCACTGCAACTTCTGCCTCCCAAGCCAAGCCATTCTCCTGCCTCTGTCTCCCGAGGAGCTGGA T G ZNF394 Ensembl:ENSG00000160908 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs964252739 Functional Loss SNV dbSNP153 33..33 33 - - - 18557 RMVar_ID_18557 Human_SNP_ID_332410064 A-to-I Human chr7 - 99497810 99497810 99497810 GTTGCCCAGGGGGAGTGCAGTGGTGTGGTCTCAGCTCACTGCAACTTCTGCCTCCCAAGCCAAGC GTTGCCCAGGGGGAGTGCAGTGGTGTGGTCTCGGCTCACTGCAACTTCTGCCTCCCAAGCCAAGC T C ZNF394 Ensembl:ENSG00000160908 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs769129169 Functional Loss SNV dbSNP153 33..33 33 - - - 18558 RMVar_ID_18558 Human_SNP_ID_332410065 A-to-I Human chr7 - 99497810 99497810 99497810 GTTGCCCAGGGGGAGTGCAGTGGTGTGGTCTCAGCTCACTGCAACTTCTGCCTCCCAAGCCAAGC GTTGCCCAGGGGGAGTGCAGTGGTGTGGTCTCCGCTCACTGCAACTTCTGCCTCCCAAGCCAAGC T G ZNF394 Ensembl:ENSG00000160908 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs769129169 Functional Loss SNV dbSNP153 33..33 33 - - - 18559 RMVar_ID_18559 Human_SNP_ID_332413311 A-to-I Human chr7 + 99508031 99508031 99508031 GCTTAGAAATACATGTGTAGGCCGGGCACGGTAGCTCATGCCTGTAATCCCAGCACTTGGGGAGG GCTTAGAAATACATGTGTAGGCCGGGCACGGTTGCTCATGCCTGTAATCCCAGCACTTGGGGAGG A T ZKSCAN5 Ensembl:ENSG00000196652 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900659326 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_336275,RMVar_hsa_circ_246962 18560 RMVar_ID_18560 Human_SNP_ID_332413703 A-to-I Human chr7 + 99509498 99509498 99509498 GCACTTTTTTTTTTTTTTTGAGACAGAGTCTCACTCTGTTGCCTAGGCTGGAGTGCAGTGGCGTG GCACTTTTTTTTTTTTTTTGAGACAGAGTCTCGCTCTGTTGCCTAGGCTGGAGTGCAGTGGCGTG A G ZKSCAN5 Ensembl:ENSG00000196652 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1324592686 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_336275,RMVar_hsa_circ_246962 18561 RMVar_ID_18561 Human_SNP_ID_332414891 A-to-I Human chr7 + 99513772 99513772 99513772 AAACAAGGCCGGGCTCAGTGGCTCACACTTGTAATCCCTGCACTTTGGGAGGCAAAGGTGGGTGG AAACAAGGCCGGGCTCAGTGGCTCACACTTGTGATCCCTGCACTTTGGGAGGCAAAGGTGGGTGG A G ZKSCAN5 Ensembl:ENSG00000196652 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1385224269 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_366409 18562 RMVar_ID_18562 Human_SNP_ID_332415803 A-to-I Human chr7 + 99517644 99517644 99517644 CGGAGGTTGCAGTTGGCCAAGATTGTATCACTACACTTCAGCCTGGGCAACAGAGCGAGACTCCA CGGAGGTTGCAGTTGGCCAAGATTGTATCACTGCACTTCAGCCTGGGCAACAGAGCGAGACTCCA A G ZKSCAN5 Ensembl:ENSG00000196652 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1256148184 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23315807 RMVar_hsa_circ_366409 18563 RMVar_ID_18563 Human_SNP_ID_332415946 A-to-I Human chr7 + 99518167 99518167 99518167 GTGCAAACTAGGGGCCAGGCACAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCATTGC GTGCAAACTAGGGGCCAGGCACAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCATTGC A G ZKSCAN5 Ensembl:ENSG00000196652 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs948188667 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_366409 18564 RMVar_ID_18564 Human_SNP_ID_332415973 A-to-I Human chr7 + 99518256 99518256 99518256 GATCCTGGACAACGTGGTGACACCCTGTCACTACTAAAACTACAAAAATTAGCCAAGCTTGGTGG GATCCTGGACAACGTGGTGACACCCTGTCACTGCTAAAACTACAAAAATTAGCCAAGCTTGGTGG A G ZKSCAN5 Ensembl:ENSG00000196652 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1472609469 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_366409 18565 RMVar_ID_18565 Human_SNP_ID_332420399 A-to-I Human chr7 + 99535784 99535784 99535784 GCCCAGGAATTCAAGATCAGCCTGGGCAACATAGTGAGATCCTCCCTACTCTGCCAGTGCCCCAC GCCCAGGAATTCAAGATCAGCCTGGGCAACATGGTGAGATCCTCCCTACTCTGCCAGTGCCCCAC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1253762373 Functional Loss SNV dbSNP153 33..33 33 - - - 18566 RMVar_ID_18566 Human_SNP_ID_332424138 A-to-I Human chr7 - 99550251 99550251 99550251 CAAAAATTAGCTGGGCCTGGTGTTGGGCGCCTATAATCCCAGCTACTCGGGAGGCTGAGGCGGAA CAAAAATTAGCTGGGCCTGGTGTTGGGCGCCTCTAATCCCAGCTACTCGGGAGGCTGAGGCGGAA T G FAM200A Ensembl:ENSG00000221909 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1217043096 Functional Loss SNV dbSNP153 33..33 33 - - - 18567 RMVar_ID_18567 Human_SNP_ID_332424402 A-to-I Human chr7 - 99551453 99551453 99551453 TGGCTCACGCCCATAATCCCAGCACTTTGGGAAGCCTAGGCAGGCGAATCGTTTGAGGCCAGGAG TGGCTCACGCCCATAATCCCAGCACTTTGGGAGGCCTAGGCAGGCGAATCGTTTGAGGCCAGGAG T C FAM200A Ensembl:ENSG00000221909 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006727981 Functional Loss SNV dbSNP153 33..33 33 - - - 18568 RMVar_ID_18568 Human_SNP_ID_332424403 A-to-I Human chr7 - 99551453 99551453 99551453 TGGCTCACGCCCATAATCCCAGCACTTTGGGAAGCCTAGGCAGGCGAATCGTTTGAGGCCAGGAG TGGCTCACGCCCATAATCCCAGCACTTTGGGACGCCTAGGCAGGCGAATCGTTTGAGGCCAGGAG T G FAM200A Ensembl:ENSG00000221909 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006727981 Functional Loss SNV dbSNP153 33..33 33 - - - 18569 RMVar_ID_18569 Human_SNP_ID_332428294 A-to-I Human chr7 + 99565345 99565345 99565345 TGCTCGCCACCATGCCTGGCTAATCTTTTCGTATTTTTAGTAGAGATGGGGTTTTGCCATCTTAG TGCTCGCCACCATGCCTGGCTAATCTTTTCGTGTTTTTAGTAGAGATGGGGTTTTGCCATCTTAG A G ZNF655,AC005020.2 Ensembl:ENSG00000197343,Ensembl:ENSG00000272647 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1468327429 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100389,RMVar_hsa_circ_246967 18570 RMVar_ID_18570 Human_SNP_ID_332428693 A-to-I Human chr7 + 99566673 99566673 99566673 TGGACTTCCCTCCAGGCTCAGGTGATCCTCCTACCTCAGCCTTCTGGGTAGCTGGGACTATAGGC TGGACTTCCCTCCAGGCTCAGGTGATCCTCCTTCCTCAGCCTTCTGGGTAGCTGGGACTATAGGC A T ZNF655,AC005020.2 Ensembl:ENSG00000197343,Ensembl:ENSG00000272647 Protein coding,Protein coding intron,intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229,31158229 RNA-Seq:(High) rs762749017 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_175569 RMVar_hsa_circ_100389,RMVar_hsa_circ_246967 18571 RMVar_ID_18571 Human_SNP_ID_332428707 A-to-I Human chr7 + 99566738 99566738 99566738 CTGTACCATCATGCTAATTTTTTTCTATTTTTAGTAAAGAAGGTGTTTCGCTATGTTACCCAGGC CTGTACCATCATGCTAATTTTTTTCTATTTTTGGTAAAGAAGGTGTTTCGCTATGTTACCCAGGC A G ZNF655,AC005020.2 Ensembl:ENSG00000197343,Ensembl:ENSG00000272647 Protein coding,Protein coding intron,intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1310024142 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_175569,Human_RBP_ID_16267904 RMVar_hsa_circ_100389,RMVar_hsa_circ_246967 18572 RMVar_ID_18572 Human_SNP_ID_332428720 A-to-I Human chr7 + 99566789 99566789 99566789 TATGTTACCCAGGCTGTTGAACTCCTGGGCTCAAGTGATCTGCATGCCTCAGCTCCCCAGAGTCC TATGTTACCCAGGCTGTTGAACTCCTGGGCTCCAGTGATCTGCATGCCTCAGCTCCCCAGAGTCC A C ZNF655,AC005020.2 Ensembl:ENSG00000197343,Ensembl:ENSG00000272647 Protein coding,Protein coding intron,intron GSE38233;GSE100210;GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;HepG2 cell line;ASD brains,frontal_cortex;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,29129909,30559470,31158229,31158229 RNA-Seq:(High) rs1410828136 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16267910 RMVar_hsa_circ_100389,RMVar_hsa_circ_246967 18573 RMVar_ID_18573 Human_SNP_ID_332428765 A-to-I Human chr7 + 99566989 99566989 99566989 TCGCTCAGGCTGGAGTGTGGTGGCACAATGTCAGCTCACTGCAACCTCCGCCTCTCAGGCCCAAG TCGCTCAGGCTGGAGTGTGGTGGCACAATGTCCGCTCACTGCAACCTCCGCCTCTCAGGCCCAAG A C ZNF655,AC005020.2 Ensembl:ENSG00000197343,Ensembl:ENSG00000272647 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs958448820 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26128723 RMVar_hsa_circ_100389,RMVar_hsa_circ_246967 18574 RMVar_ID_18574 Human_SNP_ID_332428818 A-to-I Human chr7 + 99567270 99567268 99567270 GAAAGCATAGAGTCGGCCAGGTGCTGTGGCTCACACATGTAATCCCAGCACTTTGGGAGGCCAAG GAAAGCATAGAGTCGGCCAGGTGCTGTGGCT__CACATGTAATCCCAGCACTTTGGGAGGCCAAG TCA T ZNF655,AC005020.2 Ensembl:ENSG00000197343,Ensembl:ENSG00000272647 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1007499063 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_100389,RMVar_hsa_circ_246967 18575 RMVar_ID_18575 Human_SNP_ID_332428828 A-to-I Human chr7 + 99567300 99567300 99567300 TCACACATGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGCGGATCACCTGAGGTTGGGAGTTCG TCACACATGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGCGGATCACCTGAGGTTGGGAGTTCG A G ZNF655,AC005020.2 Ensembl:ENSG00000197343,Ensembl:ENSG00000272647 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1182502619 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100389,RMVar_hsa_circ_246967 18576 RMVar_ID_18576 Human_SNP_ID_332428992 A-to-I Human chr7 + 99567912 99567912 99567912 GAAACCCCGTCTCTACTAAAAATACAAAAATTAGCTGGGCATGGTGGTACATGCCTGTGATTGCA GAAACCCCGTCTCTACTAAAAATACAAAAATTGGCTGGGCATGGTGGTACATGCCTGTGATTGCA A G ZNF655,AC005020.2 Ensembl:ENSG00000197343,Ensembl:ENSG00000272647 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1391494560 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_175570 RMVar_hsa_circ_100389,RMVar_hsa_circ_246967 18577 RMVar_ID_18577 Human_SNP_ID_332428993 A-to-I Human chr7 + 99567912 99567912 99567912 GAAACCCCGTCTCTACTAAAAATACAAAAATTAGCTGGGCATGGTGGTACATGCCTGTGATTGCA GAAACCCCGTCTCTACTAAAAATACAAAAATTTGCTGGGCATGGTGGTACATGCCTGTGATTGCA A T ZNF655,AC005020.2 Ensembl:ENSG00000197343,Ensembl:ENSG00000272647 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1391494560 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_175570 RMVar_hsa_circ_100389,RMVar_hsa_circ_246967 18578 RMVar_ID_18578 Human_SNP_ID_332428998 A-to-I Human chr7 + 99567920 99567920 99567920 GTCTCTACTAAAAATACAAAAATTAGCTGGGCATGGTGGTACATGCCTGTGATTGCAGCTACCCA GTCTCTACTAAAAATACAAAAATTAGCTGGGCCTGGTGGTACATGCCTGTGATTGCAGCTACCCA A C ZNF655,AC005020.2 Ensembl:ENSG00000197343,Ensembl:ENSG00000272647 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017812568 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_175570 RMVar_hsa_circ_100389,RMVar_hsa_circ_246967 18579 RMVar_ID_18579 Human_SNP_ID_332429009 A-to-I Human chr7 + 99567979 99567975 99567980 TACCCAGGAGGCTGAGGCTGGAGAATCGCTTGAACCCGGGAGGTGGAGGTTGCAGTGAGCCAAGA TACCCAGGAGGCTGAGGCTGGAGAATCGC_____CCCGGGAGGTGGAGGTTGCAGTGAGCCAAGA CTTGAA C ZNF655,AC005020.2 Ensembl:ENSG00000197343,Ensembl:ENSG00000272647 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903533272 Functional Loss DEL dbSNP153 30..34 33 - - - RMVar_hsa_circ_100389,RMVar_hsa_circ_246967 18580 RMVar_ID_18580 Human_SNP_ID_332429151 A-to-I Human chr7 + 99568426 99568426 99568426 GCACCCGCCATCACGCCCGGCTAATTTTTGGTATTTTTAGTAGAGACAGGGTTTCACCGTGTTAG GCACCCGCCATCACGCCCGGCTAATTTTTGGTGTTTTTAGTAGAGACAGGGTTTCACCGTGTTAG A G ZNF655,AC005020.2 Ensembl:ENSG00000197343,Ensembl:ENSG00000272647 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs959446578 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100389,RMVar_hsa_circ_246967 18581 RMVar_ID_18581 Human_SNP_ID_332429156 A-to-I Human chr7 + 99568441 99568440 99568442 CCCGGCTAATTTTTGGTATTTTTAGTAGAGACAGGGTTTCACCGTGTTAGCCAGGATGGTCTCGA CCCGGCTAATTTTTGGTATTTTTAGTAGAGAC__GGTTTCACCGTGTTAGCCAGGATGGTCTCGA CAG C ZNF655,AC005020.2 Ensembl:ENSG00000197343,Ensembl:ENSG00000272647 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1409123561 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_100389,RMVar_hsa_circ_246967 18582 RMVar_ID_18582 Human_SNP_ID_332429158 A-to-I Human chr7 + 99568441 99568441 99568441 CCCGGCTAATTTTTGGTATTTTTAGTAGAGACAGGGTTTCACCGTGTTAGCCAGGATGGTCTCGA CCCGGCTAATTTTTGGTATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGGTCTCGA A G ZNF655,AC005020.2 Ensembl:ENSG00000197343,Ensembl:ENSG00000272647 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1187613608 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100389,RMVar_hsa_circ_246967 18583 RMVar_ID_18583 Human_SNP_ID_332430632 A-to-I Human chr7 + 99574502 99574502 99574502 TGGCCTCAAGCGATCCTCCCACCTGTCCTCCCAAAGTGCTGGGGTTACAGGCGTGTGTCACTGTG TGGCCTCAAGCGATCCTCCCACCTGTCCTCCCCAAGTGCTGGGGTTACAGGCGTGTGTCACTGTG A C ZNF655,AC005020.2 Ensembl:ENSG00000197343,Ensembl:ENSG00000272647 Protein coding,Protein coding 3'UTR,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1416337919 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26550719 RMVar_hsa_circ_100389,RMVar_hsa_circ_246967,RMVar_hsa_circ_98491,RMVar_hsa_circ_246969 18584 RMVar_ID_18584 Human_SNP_ID_332430809 A-to-I Human chr7 + 99575277 99575277 99575277 AGAAGATACACAGGCCGGGCATGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGC AGAAGATACACAGGCCGGGCATGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGC A G ZNF655,AC005020.2 Ensembl:ENSG00000197343,Ensembl:ENSG00000272647 Protein coding,Protein coding 3'UTR,intron GSE47997;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 23474544,29129909,29796672,31158229,31158229 RNA-Seq:(High) rs1018384699 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100389,RMVar_hsa_circ_246967,RMVar_hsa_circ_98491,RMVar_hsa_circ_246969 18585 RMVar_ID_18585 Human_SNP_ID_332445072 A-to-I Human chr7 + 99633589 99633588 99633590 TAGCTTTTTGCTTTTATTGGTTTTTTTGAGACAGAGTCTTGCTCTGTCACCCAGGCTGGAATGCA TAGCTTTTTGCTTTTATTGGTTTTTTTGAGAC__AGTCTTGCTCTGTCACCCAGGCTGGAATGCA CAG C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388688685 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_118464,RMVar_hsa_circ_246979 18586 RMVar_ID_18586 Human_SNP_ID_332452687 A-to-I Human chr7 - 99667067 99667067 99667067 TAATGTGAGAAAAAATGTTTCTGTTGAACTCTAGTCTTTAGGCCCAGTGGGATTTATGAAAAGTG TAATGTGAGAAAAAATGTTTCTGTTGAACTCTGGTCTTTAGGCCCAGTGGGATTTATGAAAAGTG T C CYP3A5 Ensembl:ENSG00000106258 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1431404870 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60140,RMVar_hsa_circ_73875,RMVar_hsa_circ_75416,RMVar_hsa_circ_352940,RMVar_hsa_circ_364645,RMVar_hsa_circ_360521,RMVar_hsa_circ_62433,RMVar_hsa_circ_351851,RMVar_hsa_circ_361678,RMVar_hsa_circ_64232,RMVar_hsa_circ_368630,RMVar_hsa_circ_57442 18587 RMVar_ID_18587 Human_SNP_ID_332497870 A-to-I Human chr7 - 99870675 99870675 99870675 CTGCCTCAACCTCCCATAGTGCTAGGATTACAAGTGTGAGCCACCACGCCCGGCCCAACTGATTT CTGCCTCAACCTCCCATAGTGCTAGGATTACAGGTGTGAGCCACCACGCCCGGCCCAACTGATTT T C RF00017-6474 RNACentral:URS000097CF0E SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1563076466 Functional Loss SNV dbSNP153 33..33 33 - - - 18588 RMVar_ID_18588 Human_SNP_ID_332507505 A-to-I Human chr7 - 99906763 99906763 99906763 TAGCTCACTGCACCCTCAAGCTGCTGGGCTCAAGTAATTTTCCTGCCTTGATCTCCCAAAGTGTT TAGCTCACTGCACCCTCAAGCTGCTGGGCTCAGGTAATTTTCCTGCCTTGATCTCCCAAAGTGTT T C TRIM4 Ensembl:ENSG00000146833 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs571333262 Functional Loss SNV dbSNP153 33..33 33 - - - 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 18589 RMVar_ID_18589 Human_SNP_ID_332507961 A-to-I Human chr7 - 99908705 99908705 99908705 GACCTGTTTCTTCAGAGATTGAACAAAGAAGAAGAAGAGACGAAGAAGAAGCTGAATGAGAACAC GACCTGTTTCTTCAGAGATTGAACAAAGAAGAGGAAGAGACGAAGAAGAAGCTGAATGAGAACAC T C TRIM4 Ensembl:ENSG00000146833 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1261919421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_85021,Human_RBP_ID_1690585,Human_RBP_ID_5533604,Human_RBP_ID_7777680,Human_RBP_ID_8238120,Human_RBP_ID_9403657,Human_RBP_ID_22110986,Human_RBP_ID_23116855,Human_RBP_ID_24549216,Human_RBP_ID_26356762,Human_RBP_ID_27829582 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,RMVar_hsa_circ_293844,RMVar_hsa_circ_352225,RMVar_hsa_circ_246984 18590 RMVar_ID_18590 Human_SNP_ID_332523174 A-to-I Human chr7 - 99968745 99968745 99968745 TCACCCTGGCTGGTCTGGAACCCCTGGGCTCAAGCGATCCACTCGCTTCAGCTTCTCAAAGTGCT TCACCCTGGCTGGTCTGGAACCCCTGGGCTCAGGCGATCCACTCGCTTCAGCTTCTCAAAGTGCT T C AZGP1 Ensembl:ENSG00000160862 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1452035274 Functional Loss SNV dbSNP153 33..33 33 - - - 18591 RMVar_ID_18591 Human_SNP_ID_332523175 A-to-I Human chr7 - 99968746 99968746 99968746 ATCACCCTGGCTGGTCTGGAACCCCTGGGCTCAAGCGATCCACTCGCTTCAGCTTCTCAAAGTGC ATCACCCTGGCTGGTCTGGAACCCCTGGGCTCGAGCGATCCACTCGCTTCAGCTTCTCAAAGTGC T C AZGP1 Ensembl:ENSG00000160862 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1380276564 Functional Loss SNV dbSNP153 33..33 33 - - - 18592 RMVar_ID_18592 Human_SNP_ID_332539595 A-to-I Human chr7 + 100031805 100031805 100031805 CCAGGTTCAAAACAAGTTCCTTGACCAGGCACAATGGCTCACACCTGTAATCCCAACACTCGAGG CCAGGTTCAAAACAAGTTCCTTGACCAGGCACGATGGCTCACACCTGTAATCCCAACACTCGAGG A G ZKSCAN1 Ensembl:ENSG00000106261 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1230178462 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21951341,Human_RBP_ID_26129086 RMVar_hsa_circ_103504,RMVar_hsa_circ_246987,RMVar_hsa_circ_77038,RMVar_hsa_circ_246992,RMVar_hsa_circ_246994 18593 RMVar_ID_18593 Human_SNP_ID_332539639 A-to-I Human chr7 + 100032004 100032004 100032004 GGGAGGCTGAGGCAGGAGGATCACTTGAGCCCAGGAGATCGAGGCTGCAGTGAGCTGTGCTCATG GGGAGGCTGAGGCAGGAGGATCACTTGAGCCCGGGAGATCGAGGCTGCAGTGAGCTGTGCTCATG A G ZKSCAN1 Ensembl:ENSG00000106261 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1279185737 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103504,RMVar_hsa_circ_246987,RMVar_hsa_circ_77038,RMVar_hsa_circ_246992,RMVar_hsa_circ_246994 18594 RMVar_ID_18594 Human_SNP_ID_332539868 A-to-I Human chr7 + 100032901 100032901 100032901 GTGGTGGCGGGCGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATGGCGTCAACCTG GTGGTGGCGGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCGTCAACCTG A G ZKSCAN1 Ensembl:ENSG00000106261 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs996268192 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103504,RMVar_hsa_circ_246987,RMVar_hsa_circ_77038,RMVar_hsa_circ_246992,RMVar_hsa_circ_246994 18595 RMVar_ID_18595 Human_SNP_ID_332544618 A-to-I Human chr7 + 100051036 100051036 100051036 CAACATGGAGAAACCCCGTCTCTACTACAAATACAAAATTAGGCGGGCGTGGTGGCACATGCCTG CAACATGGAGAAACCCCGTCTCTACTACAAATGCAAAATTAGGCGGGCGTGGTGGCACATGCCTG A G ZSCAN21 Ensembl:ENSG00000166529 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1460669941 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107456,RMVar_hsa_circ_246998 18596 RMVar_ID_18596 Human_SNP_ID_332544619 A-to-I Human chr7 + 100051039 100051039 100051039 CATGGAGAAACCCCGTCTCTACTACAAATACAAAATTAGGCGGGCGTGGTGGCACATGCCTGTAA CATGGAGAAACCCCGTCTCTACTACAAATACAGAATTAGGCGGGCGTGGTGGCACATGCCTGTAA A G ZSCAN21 Ensembl:ENSG00000166529 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1562842142 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107456,RMVar_hsa_circ_246998 18597 RMVar_ID_18597 Human_SNP_ID_332544620 A-to-I Human chr7 + 100051044 100051044 100051044 AGAAACCCCGTCTCTACTACAAATACAAAATTAGGCGGGCGTGGTGGCACATGCCTGTAAGGAGG AGAAACCCCGTCTCTACTACAAATACAAAATTCGGCGGGCGTGGTGGCACATGCCTGTAAGGAGG A C ZSCAN21 Ensembl:ENSG00000166529 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1250991361 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107456,RMVar_hsa_circ_246998 18598 RMVar_ID_18598 Human_SNP_ID_332545665 A-to-I Human chr7 + 100054510 100054510 100054510 GACCTCAGGTGATCCACCTGCCTCGGTCTCCCAAAGTGCTGGGATTACAGGCGTGAGTCACCGCA GACCTCAGGTGATCCACCTGCCTCGGTCTCCCGAAGTGCTGGGATTACAGGCGTGAGTCACCGCA A G ZSCAN21 Ensembl:ENSG00000166529 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs554615981 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107456,RMVar_hsa_circ_246998 18599 RMVar_ID_18599 Human_SNP_ID_332548297 A-to-I Human chr7 - 100064165 100064161 100064166 GTCATAGGGCCGGTCCACCAAGTGTGTTCTGTAGTGGAGGGTGAGGTTTGAGCTGTGGCTGAAAG GTCATAGGGCCGGTCCACCAAGTGTGTTCTG_____GAGGGTGAGGTTTGAGCTGTGGCTGAAAG CCACTA C ZNF3 Ensembl:ENSG00000166526 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1229179654 Functional Loss DEL dbSNP153 32..36 33 - - - Human_RBP_ID_24234881 18600 RMVar_ID_18600 Human_SNP_ID_332549374 A-to-I Human chr7 - 100067683 100067683 100067683 TTCATGTATTAATCAGCTGGGTGCAGTGGCTCACGCCTGTAATCTCAGCACTCTGGGAGGGTAAG TTCATGTATTAATCAGCTGGGTGCAGTGGCTCGCGCCTGTAATCTCAGCACTCTGGGAGGGTAAG T C ZNF3 Ensembl:ENSG00000166526 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs796260459 Functional Loss SNV dbSNP153 33..33 33 - - - 18601 RMVar_ID_18601 Human_SNP_ID_332549375 A-to-I Human chr7 - 100067691 100067691 100067691 GAGTGGTTTTCATGTATTAATCAGCTGGGTGCAGTGGCTCACGCCTGTAATCTCAGCACTCTGGG GAGTGGTTTTCATGTATTAATCAGCTGGGTGCGGTGGCTCACGCCTGTAATCTCAGCACTCTGGG T C ZNF3 Ensembl:ENSG00000166526 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1343668063 Functional Loss SNV dbSNP153 33..33 33 - - - 18602 RMVar_ID_18602 Human_SNP_ID_332549610 A-to-I Human chr7 - 100068509 100068509 100068509 ACCACCACGCCCAGCTAACTTTTGTATTTTTAATAGACAACGGGATTTCACCATGTTGGCCAGGC ACCACCACGCCCAGCTAACTTTTGTATTTTTAGTAGACAACGGGATTTCACCATGTTGGCCAGGC T C ZNF3 Ensembl:ENSG00000166526 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1313705295 Functional Loss SNV dbSNP153 33..33 33 - - - 18603 RMVar_ID_18603 Human_SNP_ID_332549973 A-to-I Human chr7 - 100069686 100069686 100069686 CTACTTGAACCCGGGAGGCGCAGGTTGTGGTGAGCTGAGATCGCGCCATTGAACTCCAGCCTGGG CTACTTGAACCCGGGAGGCGCAGGTTGTGGTGGGCTGAGATCGCGCCATTGAACTCCAGCCTGGG T C ZNF3 Ensembl:ENSG00000166526 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1258267141 Functional Loss SNV dbSNP153 33..33 33 - - - 18604 RMVar_ID_18604 Human_SNP_ID_332549985 A-to-I Human chr7 - 100069738 100069738 100069738 ATGGTGGCACATGCCTATAATCCTAGCTACTCAGGAGGCTGAGCCAGGAGAACTACTTGAACCCG ATGGTGGCACATGCCTATAATCCTAGCTACTCGGGAGGCTGAGCCAGGAGAACTACTTGAACCCG T C ZNF3 Ensembl:ENSG00000166526 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs958610950 Functional Loss SNV dbSNP153 33..33 33 - - - 18605 RMVar_ID_18605 Human_SNP_ID_332551263 A-to-I Human chr7 - 100074114 100074114 100074114 GTTTCACTCTTGTTGCCAGGCTGGAGTGCAATAGCGTGGTCTCGGCTCACCGCAACCTCTGCGTC GTTTCACTCTTGTTGCCAGGCTGGAGTGCAATCGCGTGGTCTCGGCTCACCGCAACCTCTGCGTC T G ZNF3 Ensembl:ENSG00000166526 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1441414189 Functional Loss SNV dbSNP153 33..33 33 - - - 18606 RMVar_ID_18606 Human_SNP_ID_332551941 A-to-I Human chr7 - 100076564 100076564 100076564 TTTGCGGCCGAGCGCGGTGGCTCACTTCTGTAATCCCAGCACTTAGGGAGGCTGAGGCGGGCAGA TTTGCGGCCGAGCGCGGTGGCTCACTTCTGTAGTCCCAGCACTTAGGGAGGCTGAGGCGGGCAGA T C ZNF3 Ensembl:ENSG00000166526 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1179832001 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_247002,RMVar_hsa_circ_273088,RMVar_hsa_circ_278870,RMVar_hsa_circ_247003,RMVar_hsa_circ_247004,RMVar_hsa_circ_329854,RMVar_hsa_circ_292169 18607 RMVar_ID_18607 Human_SNP_ID_332552403 A-to-I Human chr7 - 100078303 100078303 100078303 TTTAGTAGAGATGGGGTTTCATCATCCTGGCCAGGCTGGTCTCGAACTCCTGACCTCGTGATTTG TTTAGTAGAGATGGGGTTTCATCATCCTGGCCGGGCTGGTCTCGAACTCCTGACCTCGTGATTTG T C ZNF3 Ensembl:ENSG00000166526 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1029703997 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_273088,RMVar_hsa_circ_247003,RMVar_hsa_circ_329854,RMVar_hsa_circ_269835,RMVar_hsa_circ_344399,RMVar_hsa_circ_247005 18608 RMVar_ID_18608 Human_SNP_ID_332552423 A-to-I Human chr7 - 100078384 100078384 100078384 TCAAGTGATTCTCCTGCTTCAGCTTCCTGAGTAGCTGGGATTACAGGCACACACCACCATGCCCA TCAAGTGATTCTCCTGCTTCAGCTTCCTGAGTGGCTGGGATTACAGGCACACACCACCATGCCCA T C ZNF3 Ensembl:ENSG00000166526 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1404778082 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_273088,RMVar_hsa_circ_247003,RMVar_hsa_circ_329854,RMVar_hsa_circ_269835,RMVar_hsa_circ_344399,RMVar_hsa_circ_247005 18609 RMVar_ID_18609 Human_SNP_ID_332552970 A-to-I Human chr7 - 100080407 100080407 100080407 TCACCATAGCCTGGAACTCCTGGGCTCAAGTAATCCTCCCACCTCAGCCTCCTAAAGTGCTGGGG TCACCATAGCCTGGAACTCCTGGGCTCAAGTAGTCCTCCCACCTCAGCCTCCTAAAGTGCTGGGG T C ZNF3 Ensembl:ENSG00000166526 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs542256991 Functional Loss SNV dbSNP153 33..33 33 - - - 18610 RMVar_ID_18610 Human_SNP_ID_332558117 A-to-I Human chr7 - 100096442 100096442 100096442 TAAAAATTGGTTGGGTGTGGTAGTGAGTGCCTATAGTCTCAGTTACTTGGGAGGCTGAGGCCGGA TAAAAATTGGTTGGGTGTGGTAGTGAGTGCCTGTAGTCTCAGTTACTTGGGAGGCTGAGGCCGGA T C MCM7 Ensembl:ENSG00000166508 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs577812301 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_49459,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_247029,RMVar_hsa_circ_35518 18611 RMVar_ID_18611 Human_SNP_ID_332559074 A-to-I Human chr7 - 100098600 100098600 100098600 GCAGACACGGGGCTCCAGATTCATCAAATTCCAGGAGATGAAGATGCAAGAACATGTGAGTTTGG GCAGACACGGGGCTCCAGATTCATCAAATTCCGGGAGATGAAGATGCAAGAACATGTGAGTTTGG T C MCM7 Ensembl:ENSG00000166508 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1222332604 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_85517,Human_RBP_ID_1053730,Human_RBP_ID_1690784,Human_RBP_ID_2050405,Human_RBP_ID_3860090,Human_RBP_ID_3972175,Human_RBP_ID_4955168,Human_RBP_ID_7778084,Human_RBP_ID_8675779,Human_RBP_ID_8914155,Human_RBP_ID_9403679,Human_RBP_ID_16270516,Human_RBP_ID_17314390,Human_RBP_ID_17426827,Human_RBP_ID_17713757,Human_RBP_ID_18107820,Human_RBP_ID_18385703,Human_RBP_ID_18888692,Human_RBP_ID_22111001,Human_RBP_ID_23080351,Human_RBP_ID_24234937,Human_RBP_ID_27118970 Human_Splice_Rec_896865,Human_Splice_Rec_896893,Human_Splice_Rec_896919,Human_Splice_Rec_896945,Human_Splice_Rec_896973,Human_Splice_Rec_896987,Human_Splice_Rec_897021,Human_Splice_Rec_897033 RMVar_hsa_circ_5850,RMVar_hsa_circ_86292,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_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_90521,RMVar_hsa_circ_113385,RMVar_hsa_circ_247029,RMVar_hsa_circ_35518,RMVar_hsa_circ_119373,RMVar_hsa_circ_247031,RMVar_hsa_circ_121768,RMVar_hsa_circ_127795,RMVar_hsa_circ_247033,RMVar_hsa_circ_247034,RMVar_hsa_circ_247037 18612 RMVar_ID_18612 Human_SNP_ID_332565847 A-to-I Human chr7 - 100114502 100114502 100114502 TTGGCCAGGCTGGTCTCGAATTCCTGACCTCAAGTGATCCGCCCGCCTCGTCCTCCCAAAGTGCT TTGGCCAGGCTGGTCTCGAATTCCTGACCTCAGGTGATCCGCCCGCCTCGTCCTCCCAAAGTGCT T C TAF6 Ensembl:ENSG00000106290 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1314838280 Functional Loss SNV dbSNP153 33..33 33 - - - 18613 RMVar_ID_18613 Human_SNP_ID_332565924 A-to-I Human chr7 - 100114793 100114793 100114793 CCAGGCTGGTCGTGAACTGCTGGGCTCAAGCGATCCTCCTACCTTGGGCTCCCAGAGTGTTGGAA CCAGGCTGGTCGTGAACTGCTGGGCTCAAGCGGTCCTCCTACCTTGGGCTCCCAGAGTGTTGGAA T C TAF6 Ensembl:ENSG00000106290 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs972093764 Functional Loss SNV dbSNP153 33..33 33 - - - 18614 RMVar_ID_18614 Human_SNP_ID_332565948 A-to-I Human chr7 - 100114899 100114898 100114899 TCAGTTTTCCCACCTCTGCCTCCTGAGTAGCTAGAACAACAGCCCTGTGCCTGCATACCCAGCTA TCAGTTTTCCCACCTCTGCCTCCTGAGTAGCT_GAACAACAGCCCTGTGCCTGCATACCCAGCTA CT C TAF6 Ensembl:ENSG00000106290 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1176252882 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_16270619 18615 RMVar_ID_18615 Human_SNP_ID_332565988 A-to-I Human chr7 - 100115080 100115080 100115080 GAAGCAGGAGGACTGCGTGAGCCCAGCAGTTCAAGACCAGCCTGGACAACATAGTGAGACTCTGT GAAGCAGGAGGACTGCGTGAGCCCAGCAGTTCGAGACCAGCCTGGACAACATAGTGAGACTCTGT T C TAF6 Ensembl:ENSG00000106290 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs898111848 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16270620 18616 RMVar_ID_18616 Human_SNP_ID_332566081 A-to-I Human chr7 - 100115479 100115479 100115479 TTTTGTATTTTTAGTAGAGAAAGGGTTTTACCATGTTGCTCAGGCTGGTCTCGAACTCCTGACCT TTTTGTATTTTTAGTAGAGAAAGGGTTTTACCGTGTTGCTCAGGCTGGTCTCGAACTCCTGACCT T C TAF6,AC073842.2 Ensembl:ENSG00000106290,Ensembl:ENSG00000242798 Protein coding,lincRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1055323177 Functional Loss SNV dbSNP153 33..33 33 - - - 18617 RMVar_ID_18617 Human_SNP_ID_332566504 A-to-I Human chr7 - 100117098 100117098 100117098 GGGACTACAGGTGCACATCACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTAA GGGACTACAGGTGCACATCACCACGCCCAGCTGATTTTTGTATTTTTAGTAGAGATGGGGTTTAA T C TAF6,AC073842.2 Ensembl:ENSG00000106290,Ensembl:ENSG00000242798 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs964061745 Functional Loss SNV dbSNP153 33..33 33 - - - 18618 RMVar_ID_18618 Human_SNP_ID_332566739 A-to-I Human chr7 - 100117921 100117921 100117921 CTGCCTCAGCAGCCTCCCGAGTAGCAGGGACTATAGGTGCCTGCCACCATGCCTGGCTAATTTTT CTGCCTCAGCAGCCTCCCGAGTAGCAGGGACTGTAGGTGCCTGCCACCATGCCTGGCTAATTTTT T C TAF6,AC073842.2 Ensembl:ENSG00000106290,Ensembl:ENSG00000242798 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935057974 Functional Loss SNV dbSNP153 33..33 33 - - - 18619 RMVar_ID_18619 Human_SNP_ID_332566952 A-to-I Human chr7 - 100118549 100118549 100118549 CAGTTCAAGCGATCCTCCTGCCTCAGCCTCCTAAGTAGCTGGGATGACAGGTTCACACCACCAGG CAGTTCAAGCGATCCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATGACAGGTTCACACCACCAGG T C TAF6,AC073842.2 Ensembl:ENSG00000106290,Ensembl:ENSG00000242798 Protein coding,lincRNA intron,intron GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829 esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line - 29796672,31158229 RNA-Seq:(High) rs988377366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26129527 Human_Splice_Rec_897563,Human_Splice_Rec_897587,Human_Splice_Rec_897595,Human_Splice_Rec_897605 18620 RMVar_ID_18620 Human_SNP_ID_332566959 A-to-I Human chr7 - 100118574 100118574 100118574 TGGCTCACTGCAGCCTCCAACTCCTCAGTTCAAGCGATCCTCCTGCCTCAGCCTCCTAAGTAGCT TGGCTCACTGCAGCCTCCAACTCCTCAGTTCAGGCGATCCTCCTGCCTCAGCCTCCTAAGTAGCT T C TAF6,AC073842.2 Ensembl:ENSG00000106290,Ensembl:ENSG00000242798 Protein coding,lincRNA intron,intron GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line - 29129909,29796672,31158229 RNA-Seq:(High) rs908956783 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_897562,Human_Splice_Rec_897563,Human_Splice_Rec_897586,Human_Splice_Rec_897587,Human_Splice_Rec_897594,Human_Splice_Rec_897595,Human_Splice_Rec_897604,Human_Splice_Rec_897605,Human_Splice_Rec_897610 18621 RMVar_ID_18621 Human_SNP_ID_332567943 A-to-I Human chr7 + 100121304 100121304 100121304 GGGATTACAGGCGCCCGCCACCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGACAAGGTTTCA GGGATTACAGGCGCCCGCCACCATGCCCAGCTGATTTTTGTATTTTTAGTAGAGACAAGGTTTCA A G CNPY4 Ensembl:ENSG00000166997 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1041269927 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_175241 RMVar_hsa_circ_247063,RMVar_hsa_circ_123795 18622 RMVar_ID_18622 Human_SNP_ID_332572680 A-to-I Human chr7 + 100136280 100136280 100136280 AGCATTTTTGTTTGTTTGTTTGTTTGAGACGGAGTCTCATTGTGTCACCCAGACTGGAGTGTAGT AGCATTTTTGTTTGTTTGTTTGTTTGAGACGGCGTCTCATTGTGTCACCCAGACTGGAGTGTAGT A C AC073842.1 Ensembl:ENSG00000235077 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1004577524 Functional Loss SNV dbSNP153 33..33 33 - - - 18623 RMVar_ID_18623 Human_SNP_ID_332576489 A-to-I Human chr7 + 100150730 100150730 100150730 AGACTGGGCTGGGCGTGGTGGTTCATGCCTGTAATTCTAGCACTTTGGGAGGCCAAGGCGGGCGG AGACTGGGCTGGGCGTGGTGGTTCATGCCTGTCATTCTAGCACTTTGGGAGGCCAAGGCGGGCGG A C LAMTOR4 Ensembl:ENSG00000188186 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1282642653 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_247066,RMVar_hsa_circ_76464 18624 RMVar_ID_18624 Human_SNP_ID_332576534 A-to-I Human chr7 + 100150842 100150842 100150842 CCCGTCTGTACTAAAAATACAAAAACAAAATTAGCCAGGCCTGGTGGCGGGCACTTGTAGTCCCA CCCGTCTGTACTAAAAATACAAAAACAAAATTGGCCAGGCCTGGTGGCGGGCACTTGTAGTCCCA A G LAMTOR4 Ensembl:ENSG00000188186 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1239634199 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_247066,RMVar_hsa_circ_76464 18625 RMVar_ID_18625 Human_SNP_ID_332576542 A-to-I Human chr7 + 100150862 100150862 100150862 AAAAACAAAATTAGCCAGGCCTGGTGGCGGGCACTTGTAGTCCCAGCTACTCGGGAAGCTGAGGC AAAAACAAAATTAGCCAGGCCTGGTGGCGGGCGCTTGTAGTCCCAGCTACTCGGGAAGCTGAGGC A G LAMTOR4 Ensembl:ENSG00000188186 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1272589430 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_247066,RMVar_hsa_circ_76464 18626 RMVar_ID_18626 Human_SNP_ID_332576627 A-to-I Human chr7 + 100151136 100151136 100151136 TCGCTCTGTGGCCCAGGCTGGAGTGCAGTGGCATGATCTCAGCTCACTGCAACCTCCGTCTTCCG TCGCTCTGTGGCCCAGGCTGGAGTGCAGTGGCGTGATCTCAGCTCACTGCAACCTCCGTCTTCCG A G LAMTOR4 Ensembl:ENSG00000188186 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1417210597 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_247066,RMVar_hsa_circ_76464 18627 RMVar_ID_18627 Human_SNP_ID_332576821 A-to-I Human chr7 + 100151800 100151800 100151800 CTCATTGTAGCCTTGAACTCCTGGGCCCAAGCAATCCTCCCGCCTCAGCATCCCAAGTAACTAGA CTCATTGTAGCCTTGAACTCCTGGGCCCAAGCCATCCTCCCGCCTCAGCATCCCAAGTAACTAGA A C LAMTOR4 Ensembl:ENSG00000188186 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1345314192 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_247066,RMVar_hsa_circ_76464 18628 RMVar_ID_18628 Human_SNP_ID_332576948 A-to-I Human chr7 + 100152327 100152327 100152327 GGGAGGTTGAGGCAGGAGAATTGCTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCCAAGATTGCA GGGAGGTTGAGGCAGGAGAATTGCTTGAACCCGGGAGGCAGAGGTTGCAGTGAGCCAAGATTGCA A G LAMTOR4 Ensembl:ENSG00000188186 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1396546141 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_247066,RMVar_hsa_circ_76464 18629 RMVar_ID_18629 Human_SNP_ID_332577080 A-to-I Human chr7 + 100152944 100152943 100152945 GGGAGGCTGAGGCGGGCAGATCATTTGAGGTCAAGAGTTTGAGACCAGCTGATTAATATGGTAAA GGGAGGCTGAGGCGGGCAGATCATTTGAGGTC__GAGTTTGAGACCAGCTGATTAATATGGTAAA CAA C LAMTOR4 Ensembl:ENSG00000188186 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1299657482 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_247066,RMVar_hsa_circ_76464 18630 RMVar_ID_18630 Human_SNP_ID_332588696 A-to-I Human chr7 - 100192698 100192698 100192698 TAGTACCAGATACTTGGAAGGATAAGGCAGGAACATCACTTGAGCACAGGAGGTTGGGGCTGCAG TAGTACCAGATACTTGGAAGGATAAGGCAGGACCATCACTTGAGCACAGGAGGTTGGGGCTGCAG T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs908304763 Functional Loss SNV dbSNP153 33..33 33 - - - 18631 RMVar_ID_18631 Human_SNP_ID_332589023 A-to-I Human chr7 - 100194223 100194223 100194223 ATTAAGCTTAGAGGCCAGGTGCAGTGGCTCACACCTATAATCCCAGCACTTTGGGTGGCCAAGGT ATTAAGCTTAGAGGCCAGGTGCAGTGGCTCACGCCTATAATCCCAGCACTTTGGGTGGCCAAGGT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1249538655 Functional Loss SNV dbSNP153 33..33 33 - - - 18632 RMVar_ID_18632 Human_SNP_ID_332589129 A-to-I Human chr7 - 100194759 100194759 100194759 ACAGGGTCTCACTCTGGCACCCAGGCTGGAGTACAGTGGTGTGACCATGGCTCACGGCAGCCTCC ACAGGGTCTCACTCTGGCACCCAGGCTGGAGTGCAGTGGTGTGACCATGGCTCACGGCAGCCTCC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1275364069 Functional Loss SNV dbSNP153 33..33 33 - - - 18633 RMVar_ID_18633 Human_SNP_ID_332593822 A-to-I Human chr7 - 100212732 100212732 100212732 AAATGGGCCCCACGCAGTGGCTCACACCTGTAATCCCAGCACTTAGGGAGGCTGAGCCAGGTGGA AAATGGGCCCCACGCAGTGGCTCACACCTGTAGTCCCAGCACTTAGGGAGGCTGAGCCAGGTGGA T C CASTOR3 Ensembl:ENSG00000239521 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line - 29129909,31158229,32596459 RNA-Seq:(High) rs1228405581 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17577503 18634 RMVar_ID_18634 Human_SNP_ID_332593849 A-to-I Human chr7 - 100212816 100212816 100212816 CCAACTCCTGGACTATTGATCCTCCTGTCTCCACCTCCCGAGTTGCTGGAACTACAGGCTAACAG CCAACTCCTGGACTATTGATCCTCCTGTCTCCGCCTCCCGAGTTGCTGGAACTACAGGCTAACAG T C CASTOR3 Ensembl:ENSG00000239521 Protein coding intron GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831 HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line - 29129909,32596459 RNA-Seq:(High) rs1165547736 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17577504 Human_miRNA_ID_136913,Human_miRNA_ID_1025104 18635 RMVar_ID_18635 Human_SNP_ID_332593861 A-to-I Human chr7 - 100212867 100212867 100212867 GTTGATTTTTTTTTAAGAGACACGTGTTTACTATGTTACCCAGGCTGGACTCCAACTCCTGGACT GTTGATTTTTTTTTAAGAGACACGTGTTTACTGTGTTACCCAGGCTGGACTCCAACTCCTGGACT T C CASTOR3 Ensembl:ENSG00000239521 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1356838172 Functional Loss SNV dbSNP153 33..33 33 - - - 18636 RMVar_ID_18636 Human_SNP_ID_332599653 A-to-I Human chr7 - 100232822 100232822 100232822 CTACTTGGGAGGCTGAGGTGGGAGGATTGCTTAAACCCAGGAGTTTGAGACTGTAGTGTGCAATG CTACTTGGGAGGCTGAGGTGGGAGGATTGCTTCAACCCAGGAGTTTGAGACTGTAGTGTGCAATG T G CASTOR3 Ensembl:ENSG00000239521 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1373285314 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_175649 RMVar_hsa_circ_93743,RMVar_hsa_circ_299180,RMVar_hsa_circ_247084 18637 RMVar_ID_18637 Human_SNP_ID_332614377 A-to-I Human chr7 - 100294126 100294126 100294126 TCGGCCAGGCTGGAGTTGAGTGGTGCCATCATAGCTCACTGCAGTCTTAAACTCCTGGGCTCAAA TCGGCCAGGCTGGAGTTGAGTGGTGCCATCATGGCTCACTGCAGTCTTAAACTCCTGGGCTCAAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223412106 Functional Loss SNV dbSNP153 33..33 33 - - - 18638 RMVar_ID_18638 Human_SNP_ID_332614415 A-to-I Human chr7 - 100294310 100294310 100294310 ATTTTGTATTTTTTTTAGGGACAAGTTTTGCCATGTTGCCCAGGCTGGTCTTAAACTCCTAGGCT ATTTTGTATTTTTTTTAGGGACAAGTTTTGCCGTGTTGCCCAGGCTGGTCTTAAACTCCTAGGCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167270939 Functional Loss SNV dbSNP153 33..33 33 - - - 18639 RMVar_ID_18639 Human_SNP_ID_332616398 A-to-I Human chr7 - 100301589 100301589 100301589 AAGACCTCATCTCTACAAAAAATACAAAAATTAGCAGGGTGTGGTGGTGCACACCTGTAGTCACA AAGACCTCATCTCTACAAAAAATACAAAAATTCGCAGGGTGTGGTGGTGCACACCTGTAGTCACA T G lnc-CASTOR3-4 RNACentral:URS0000D5B10A lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1304173795 Functional Loss SNV dbSNP153 33..33 33 - - - 18640 RMVar_ID_18640 Human_SNP_ID_332623380 A-to-I Human chr7 - 100328241 100328241 100328241 ACCATTACAGGCACGCGCCACCACGCCCAGCTAATTTTTGTATTTTCAGTGGAGACGGGGTTCCA ACCATTACAGGCACGCGCCACCACGCCCAGCTGATTTTTGTATTTTCAGTGGAGACGGGGTTCCA T C PMS2P1 Ensembl:ENSG00000078319 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1411130521 Functional Loss SNV dbSNP153 33..33 33 - - - 18641 RMVar_ID_18641 Human_SNP_ID_332623403 A-to-I Human chr7 - 100328306 100328306 100328306 CAGTTCACTGCAACCTCCACCTGCCAAGTTCAAGCGATTCTCCTGCTTCAGCCTTCTGAGTAGCT CAGTTCACTGCAACCTCCACCTGCCAAGTTCACGCGATTCTCCTGCTTCAGCCTTCTGAGTAGCT T G PMS2P1 Ensembl:ENSG00000078319 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs184316567 Functional Loss SNV dbSNP153 33..33 33 - - - 18642 RMVar_ID_18642 Human_SNP_ID_332623448 A-to-I Human chr7 - 100328458 100328455 100328459 GCGTCACTGCACTTCAGACTGTGAGACAGAGTAAGACCCTGTCTGGAAAAATATATATACATATA GCGTCACTGCACTTCAGACTGTGAGACAGAG____ACCCTGTCTGGAAAAATATATATACATATA TCTTA T PMS2P1 Ensembl:ENSG00000078319 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285760673 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_17577842 18643 RMVar_ID_18643 Human_SNP_ID_332623459 A-to-I Human chr7 - 100328496 100328496 100328496 TTGAGCCCGGGAACTTGAGACTGCAGTGAGCTATGATTGCGTCACTGCACTTCAGACTGTGAGAC TTGAGCCCGGGAACTTGAGACTGCAGTGAGCTGTGATTGCGTCACTGCACTTCAGACTGTGAGAC T C PMS2P1 Ensembl:ENSG00000078319 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs534192586 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17577842 18644 RMVar_ID_18644 Human_SNP_ID_332623460 A-to-I Human chr7 - 100328496 100328496 100328496 TTGAGCCCGGGAACTTGAGACTGCAGTGAGCTATGATTGCGTCACTGCACTTCAGACTGTGAGAC TTGAGCCCGGGAACTTGAGACTGCAGTGAGCTCTGATTGCGTCACTGCACTTCAGACTGTGAGAC T G PMS2P1 Ensembl:ENSG00000078319 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs534192586 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17577842 18645 RMVar_ID_18645 Human_SNP_ID_332626430 A-to-I Human chr7 + 100339137 100339137 100339137 TTGCCCAGGCTGGAGTGCAGTGGCACAGTCTCAGCTCACTGCAGCCTCTGCCTCCTGGGTTCAAG TTGCCCAGGCTGGAGTGCAGTGGCACAGTCTCGGCTCACTGCAGCCTCTGCCTCCTGGGTTCAAG A G STAG3L5P,STAG3L5P-PVRIG2P-PILRB Ensembl:ENSG00000242294,Ensembl:ENSG00000272752 Pseudogene,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs577697467 Functional Loss SNV dbSNP153 33..33 33 - - - 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 18646 RMVar_ID_18646 Human_SNP_ID_332627545 A-to-I Human chr7 + 100343463 100343463 100343463 CGGTCTGTCACCCAGGCTGGAATTGCAGTGGCACGATCTCAGCTCACTGCAAGCTCCACCTCCTG CGGTCTGTCACCCAGGCTGGAATTGCAGTGGCGCGATCTCAGCTCACTGCAAGCTCCACCTCCTG A G STAG3L5P,STAG3L5P-PVRIG2P-PILRB Ensembl:ENSG00000242294,Ensembl:ENSG00000272752 Pseudogene,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1412562632 Functional Loss SNV dbSNP153 33..33 33 - - - 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 18647 RMVar_ID_18647 Human_SNP_ID_332627606 A-to-I Human chr7 + 100343669 100343669 100343669 TGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGAGATTATAGGCGTGAGCCACCGCGCCCGGCCAC TGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTATAGGCGTGAGCCACCGCGCCCGGCCAC A G STAG3L5P,STAG3L5P-PVRIG2P-PILRB Ensembl:ENSG00000242294,Ensembl:ENSG00000272752 Pseudogene,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1441525570 Functional Loss SNV dbSNP153 33..33 33 - - - 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 18648 RMVar_ID_18648 Human_SNP_ID_332627607 A-to-I Human chr7 + 100343674 100343674 100343674 CGCCCGCCTCGGCCTCCCAAAGTGCTGAGATTATAGGCGTGAGCCACCGCGCCCGGCCACCCTTT CGCCCGCCTCGGCCTCCCAAAGTGCTGAGATTGTAGGCGTGAGCCACCGCGCCCGGCCACCCTTT A G STAG3L5P,STAG3L5P-PVRIG2P-PILRB Ensembl:ENSG00000242294,Ensembl:ENSG00000272752 Pseudogene,lincRNA intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1052018188 Functional Loss SNV dbSNP153 33..33 33 - - - 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 18649 RMVar_ID_18649 Human_SNP_ID_332627679 A-to-I Human chr7 + 100343953 100343953 100343953 AAAATACAACAAAATTGGTGGCATGCGCCTGTAGTCCCAGCTACTCAGGAGGCTCAGACAGGAGA AAAATACAACAAAATTGGTGGCATGCGCCTGTCGTCCCAGCTACTCAGGAGGCTCAGACAGGAGA A C STAG3L5P,STAG3L5P-PVRIG2P-PILRB Ensembl:ENSG00000242294,Ensembl:ENSG00000272752 Pseudogene,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1482975581 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26129809 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 18650 RMVar_ID_18650 Human_SNP_ID_332627682 A-to-I Human chr7 + 100343967 100343967 100343967 TTGGTGGCATGCGCCTGTAGTCCCAGCTACTCAGGAGGCTCAGACAGGAGAATCGCTTGAACCCG TTGGTGGCATGCGCCTGTAGTCCCAGCTACTCGGGAGGCTCAGACAGGAGAATCGCTTGAACCCG A G STAG3L5P,STAG3L5P-PVRIG2P-PILRB Ensembl:ENSG00000242294,Ensembl:ENSG00000272752 Pseudogene,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893720873 Functional Loss SNV dbSNP153 33..33 33 - - - 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 18651 RMVar_ID_18651 Human_SNP_ID_332627707 A-to-I Human chr7 + 100344031 100344025 100344031 GGGAGACGGAGGTTGCAGTGAACCGAGATTGCACCACTGCACTCCAGCCTGGCAACTGGACGAGA GGGAGACGGAGGTTGCAGTGAACCGAG______CCACTGCACTCCAGCCTGGCAACTGGACGAGA GATTGCA G STAG3L5P,STAG3L5P-PVRIG2P-PILRB Ensembl:ENSG00000242294,Ensembl:ENSG00000272752 Pseudogene,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs3069829 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_26129811 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 18652 RMVar_ID_18652 Human_SNP_ID_332630106 A-to-I Human chr7 + 100352794 100352792 100352794 CCCGCTGGGAAACCCAGAGCAGCATCTCTCTCATCCTGGAAGGCTCTGGGGCCAGCAGCCCCTGC CCCGCTGGGAAACCCAGAGCAGCATCTCTCT__TCCTGGAAGGCTCTGGGGCCAGCAGCCCCTGC TCA T PILRB,STAG3L5P-PVRIG2P-PILRB,PVRIG2P Ensembl:ENSG00000121716,Ensembl:ENSG00000272752,Ensembl:ENSG00000235333 Protein coding,lincRNA,Pseudogene 5'UTR,exon,exon GSE107867 ASD brains,cerebellum;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs763398821 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_17430162 Human_Splice_Rec_898670,Human_Splice_Rec_898812 RMVar_hsa_circ_48532,RMVar_hsa_circ_93853,RMVar_hsa_circ_77737,RMVar_hsa_circ_247091,RMVar_hsa_circ_247092 18653 RMVar_ID_18653 Human_SNP_ID_332630108 A-to-I Human chr7 - 100352795 100352793 100352795 CGCAGGGGCTGCTGGCCCCAGAGCCTTCCAGGATGAGAGAGATGCTGCTCTGGGTTTCCCAGCGG CGCAGGGGCTGCTGGCCCCAGAGCCTTCCAGGGCAAGAGAGATGCTGCTCTGGGTTTCCCAGCGG CAT TGC - - Other Unknown GSE107867 ASD brains,cerebellum;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs796556542 Functional Loss MNV dbSNP153 33..35 33 - - - 18654 RMVar_ID_18654 Human_SNP_ID_332630108 A-to-I Human chr7 + 100352794 100352793 100352795 CCCGCTGGGAAACCCAGAGCAGCATCTCTCTCATCCTGGAAGGCTCTGGGGCCAGCAGCCCCTGC CCCGCTGGGAAACCCAGAGCAGCATCTCTCTTGCCCTGGAAGGCTCTGGGGCCAGCAGCCCCTGC CAT TGC PILRB,STAG3L5P-PVRIG2P-PILRB,PVRIG2P Ensembl:ENSG00000121716,Ensembl:ENSG00000272752,Ensembl:ENSG00000235333 Protein coding,lincRNA,Pseudogene 5'UTR,exon,exon GSE107867 ASD brains,cerebellum;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs796556542 Functional Loss MNV dbSNP153 32..34 33 - - - Human_RBP_ID_17430162 Human_Splice_Rec_898670,Human_Splice_Rec_898812 RMVar_hsa_circ_48532,RMVar_hsa_circ_93853,RMVar_hsa_circ_77737,RMVar_hsa_circ_247091,RMVar_hsa_circ_247092 18655 RMVar_ID_18655 Human_SNP_ID_332630109 A-to-I Human chr7 + 100352794 100352794 100352794 CCCGCTGGGAAACCCAGAGCAGCATCTCTCTCATCCTGGAAGGCTCTGGGGCCAGCAGCCCCTGC CCCGCTGGGAAACCCAGAGCAGCATCTCTCTCGTCCTGGAAGGCTCTGGGGCCAGCAGCCCCTGC A G PILRB,STAG3L5P-PVRIG2P-PILRB,PVRIG2P Ensembl:ENSG00000121716,Ensembl:ENSG00000272752,Ensembl:ENSG00000235333 Protein coding,lincRNA,Pseudogene 5'UTR,exon,exon GSE107867 ASD brains,cerebellum;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs547186306 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17430162 Human_Splice_Rec_898670,Human_Splice_Rec_898812 RMVar_hsa_circ_48532,RMVar_hsa_circ_93853,RMVar_hsa_circ_77737,RMVar_hsa_circ_247091,RMVar_hsa_circ_247092 18656 RMVar_ID_18656 Human_SNP_ID_332630110 A-to-I Human chr7 - 100352795 100352795 100352795 CGCAGGGGCTGCTGGCCCCAGAGCCTTCCAGGATGAGAGAGATGCTGCTCTGGGTTTCCCAGCGG CGCAGGGGCTGCTGGCCCCAGAGCCTTCCAGGGTGAGAGAGATGCTGCTCTGGGTTTCCCAGCGG T C - - Other Unknown GSE107867 ASD brains,cerebellum;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs559354079 Functional Loss SNV dbSNP153 33..33 33 - - - 18657 RMVar_ID_18657 Human_SNP_ID_332630626 A-to-I Human chr7 + 100354510 100354510 100354510 CTCCTGCGTCAGCCTCCCGAGTAGCTGGGACTACGGATGTGCACCATCGTGTCCGCTAATTTTTG CTCCTGCGTCAGCCTCCCGAGTAGCTGGGACTGCGGATGTGCACCATCGTGTCCGCTAATTTTTG A G PILRB,STAG3L5P-PVRIG2P-PILRB Ensembl:ENSG00000121716,Ensembl:ENSG00000272752 Protein coding,lincRNA intron,intron GSE100210;GSE107867 HepG2 cell line;ASD brains,cerebellum - 29129909,30559470 RNA-Seq:(High) rs1471707284 Functional Loss SNV dbSNP153 33..33 33 - - - 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 18658 RMVar_ID_18658 Human_SNP_ID_332631013 A-to-I Human chr7 + 100356059 100356059 100356059 GTGGCACACACCTGTAATTCCCAGCTACTTGGAAGGCTGAGGCAGGAGAATTACTTGAACCCAGG GTGGCACACACCTGTAATTCCCAGCTACTTGGCAGGCTGAGGCAGGAGAATTACTTGAACCCAGG A C PILRB,STAG3L5P-PVRIG2P-PILRB Ensembl:ENSG00000121716,Ensembl:ENSG00000272752 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1440520261 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2314,RMVar_hsa_circ_64288,RMVar_hsa_circ_247097,RMVar_hsa_circ_315939,RMVar_hsa_circ_369647,RMVar_hsa_circ_304343,RMVar_hsa_circ_277057,RMVar_hsa_circ_247099,RMVar_hsa_circ_247100,RMVar_hsa_circ_247098 18659 RMVar_ID_18659 Human_SNP_ID_332632267 A-to-I Human chr7 + 100359821 100359821 100359821 CCAAGGCAGGTGGATCACAAGGCCAAGAGATCAAGACCATCCTGGCCAACATGGTGACACCCCAT CCAAGGCAGGTGGATCACAAGGCCAAGAGATCGAGACCATCCTGGCCAACATGGTGACACCCCAT A G PILRB,STAG3L5P-PVRIG2P-PILRB Ensembl:ENSG00000121716,Ensembl:ENSG00000272752 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1397893591 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23079968 RMVar_hsa_circ_247100 18660 RMVar_ID_18660 Human_SNP_ID_332632601 A-to-I Human chr7 + 100360999 100360999 100360999 GTTCTGTCGCCCAGGCTGGAGTGCAGTGGCACAATCTCGGCTCACTGCAAGCTCCCCCTCCTGGG GTTCTGTCGCCCAGGCTGGAGTGCAGTGGCACGATCTCGGCTCACTGCAAGCTCCCCCTCCTGGG A G PILRB,STAG3L5P-PVRIG2P-PILRB Ensembl:ENSG00000121716,Ensembl:ENSG00000272752 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1015493125 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_247100 18661 RMVar_ID_18661 Human_SNP_ID_332632728 A-to-I Human chr7 + 100361434 100361434 100361434 AGTCTTCAGGCCAGGCACGGTGGCTAATGCCTATAATCCCAGCACCTTGGGAGGCCAAGGCGGCT AGTCTTCAGGCCAGGCACGGTGGCTAATGCCTGTAATCCCAGCACCTTGGGAGGCCAAGGCGGCT A G PILRB,STAG3L5P-PVRIG2P-PILRB Ensembl:ENSG00000121716,Ensembl:ENSG00000272752 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs896500758 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5251398 RMVar_hsa_circ_247100 18662 RMVar_ID_18662 Human_SNP_ID_332632741 A-to-I Human chr7 + 100361482 100361482 100361482 GGGAGGCCAAGGCGGCTGGATCACCTGAGGTCAGGCGTTCAAGACCAGCCTGGCCAAAATGGTGA GGGAGGCCAAGGCGGCTGGATCACCTGAGGTCCGGCGTTCAAGACCAGCCTGGCCAAAATGGTGA A C PILRB,STAG3L5P-PVRIG2P-PILRB Ensembl:ENSG00000121716,Ensembl:ENSG00000272752 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1400659645 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5251398 RMVar_hsa_circ_247100 18663 RMVar_ID_18663 Human_SNP_ID_332633019 A-to-I Human chr7 + 100362588 100362588 100362588 TGGAGTGCAGTGGTGCCATCTTGGCTCACTGCAACTTCTGCCTCCCGGGTTCAAGCGATTCTTCC TGGAGTGCAGTGGTGCCATCTTGGCTCACTGCGACTTCTGCCTCCCGGGTTCAAGCGATTCTTCC A G PILRB,STAG3L5P-PVRIG2P-PILRB Ensembl:ENSG00000121716,Ensembl:ENSG00000272752 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs111514415 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_247100 18664 RMVar_ID_18664 Human_SNP_ID_332633049 A-to-I Human chr7 + 100362711 100362711 100362711 TTGTATTTTTGGAAGAAACGTGGTTTTACTATATTGGCCAGGCTGGTCTCGAACTCCCGACCTCA TTGTATTTTTGGAAGAAACGTGGTTTTACTATGTTGGCCAGGCTGGTCTCGAACTCCCGACCTCA A G PILRB,STAG3L5P-PVRIG2P-PILRB Ensembl:ENSG00000121716,Ensembl:ENSG00000272752 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs760433294 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5251402 RMVar_hsa_circ_247100 18665 RMVar_ID_18665 Human_SNP_ID_332633336 A-to-I Human chr7 + 100363961 100363961 100363961 AGAAACCCCATCTCTACTAAAAATACAAAATTAGCCAGGCGTGGTGGCGCATGTCTGTAATCCCA AGAAACCCCATCTCTACTAAAAATACAAAATTGGCCAGGCGTGGTGGCGCATGTCTGTAATCCCA A G PILRB,STAG3L5P-PVRIG2P-PILRB Ensembl:ENSG00000121716,Ensembl:ENSG00000272752 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1314076681 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_247100 18666 RMVar_ID_18666 Human_SNP_ID_332633596 A-to-I Human chr7 + 100364914 100364914 100364914 AGGTTGAGGGTGTAGTGAACTATGATTGTGCCACTGCACTCCATCCTGGGTGACAGTATAAGATC AGGTTGAGGGTGTAGTGAACTATGATTGTGCCTCTGCACTCCATCCTGGGTGACAGTATAAGATC A T PILRB,STAG3L5P-PVRIG2P-PILRB Ensembl:ENSG00000121716,Ensembl:ENSG00000272752 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1314707710 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23080001 RMVar_hsa_circ_247100 18667 RMVar_ID_18667 Human_SNP_ID_332633636 A-to-I Human chr7 + 100365023 100365023 100365023 AATCTTTTTTATTTAGTTATTTATTTTGAGACAAAGTCCTGCTTTGTCACCCAGGCTGGAGTGCA AATCTTTTTTATTTAGTTATTTATTTTGAGACGAAGTCCTGCTTTGTCACCCAGGCTGGAGTGCA A G PILRB,STAG3L5P-PVRIG2P-PILRB Ensembl:ENSG00000121716,Ensembl:ENSG00000272752 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1307710725 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3120524,Human_RBP_ID_3860191,Human_RBP_ID_16271813 RMVar_hsa_circ_247100 18668 RMVar_ID_18668 Human_SNP_ID_332633805 A-to-I Human chr7 + 100365635 100365635 100365635 GAGGCCTGGAGTTCGAGCCCAGCCTGGCCAACATGGCGAAACCCTGTCTCTACTAAAAATACAAA GAGGCCTGGAGTTCGAGCCCAGCCTGGCCAACGTGGCGAAACCCTGTCTCTACTAAAAATACAAA A G PILRB,STAG3L5P-PVRIG2P-PILRB Ensembl:ENSG00000121716,Ensembl:ENSG00000272752 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs988383852 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_247100 18669 RMVar_ID_18669 Human_SNP_ID_332633839 A-to-I Human chr7 + 100365773 100365773 100365773 CCAGGAGATGGAGGTTGCAGTGAGCTGAGATCACGTCACTGTATAGCAGCCTGGGTGACACAGCA CCAGGAGATGGAGGTTGCAGTGAGCTGAGATCGCGTCACTGTATAGCAGCCTGGGTGACACAGCA A G PILRB,STAG3L5P-PVRIG2P-PILRB Ensembl:ENSG00000121716,Ensembl:ENSG00000272752 Protein coding,lincRNA intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs979189473 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3120531 RMVar_hsa_circ_247100 18670 RMVar_ID_18670 Human_SNP_ID_332633982 A-to-I Human chr7 + 100366156 100366156 100366156 TTGTAATTTTAGTAGAGACAGGTTTTCACCATATTGTTCAGGCTGATCTCGAACTCCTGACCTCA TTGTAATTTTAGTAGAGACAGGTTTTCACCATGTTGTTCAGGCTGATCTCGAACTCCTGACCTCA A G PILRB,STAG3L5P-PVRIG2P-PILRB Ensembl:ENSG00000121716,Ensembl:ENSG00000272752 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1289523027 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5251405 RMVar_hsa_circ_247100 18671 RMVar_ID_18671 Human_SNP_ID_332633994 A-to-I Human chr7 + 100366188 100366188 100366188 ATTGTTCAGGCTGATCTCGAACTCCTGACCTCAGGTGATCTGCCCACCTTGGCCTCCCAATCCTG ATTGTTCAGGCTGATCTCGAACTCCTGACCTCGGGTGATCTGCCCACCTTGGCCTCCCAATCCTG A G PILRB,STAG3L5P-PVRIG2P-PILRB Ensembl:ENSG00000121716,Ensembl:ENSG00000272752 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1364784564 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5251405 RMVar_hsa_circ_247100 18672 RMVar_ID_18672 Human_SNP_ID_332634829 A-to-I Human chr7 + 100369023 100369023 100369023 TCAGGTGGCAACTGAGGCTGCAGTGAGTTGTGATTGCACCACTGTACTCCAGCCTGGGTGACAGA TCAGGTGGCAACTGAGGCTGCAGTGAGTTGTGTTTGCACCACTGTACTCCAGCCTGGGTGACAGA A T PILRA Ensembl:ENSG00000085514 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1563112140 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22327449 18673 RMVar_ID_18673 Human_SNP_ID_332653594 A-to-I Human chr7 + 100437903 100437903 100437903 CACCACACCCGGCTAATTTTTTTTGTATTTTTAGTAGAGACAGGGTTTCACCGTGTTGGCCTCGA CACCACACCCGGCTAATTTTTTTTGTATTTTTGGTAGAGACAGGGTTTCACCGTGTTGGCCTCGA A G PPP1R35-AS1 Ensembl:ENSG00000240211 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs541974748 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7666316 18674 RMVar_ID_18674 Human_SNP_ID_332661724 A-to-I Human chr7 - 100469105 100469105 100469105 CTCCTGCCTCAGCCTCCAGAGTAGCTAGGATTACAGGCACCCCCCACCATGCCCAGCTAATTTTT CTCCTGCCTCAGCCTCCAGAGTAGCTAGGATTGCAGGCACCCCCCACCATGCCCAGCTAATTTTT T C TSC22D4 Ensembl:ENSG00000166925 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1337665399 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16002 18675 RMVar_ID_18675 Human_SNP_ID_332683507 A-to-I Human chr7 + 100550186 100550186 100550186 AAAATTAGCTGGGCGTGGTGGCGCATGCCTATAGTCTCAGCTACTTGGGAGACTGAGGCAGGAGA AAAATTAGCTGGGCGTGGTGGCGCATGCCTATGGTCTCAGCTACTTGGGAGACTGAGGCAGGAGA A G AGFG2 Ensembl:ENSG00000106351 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1045862511 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73175,RMVar_hsa_circ_247109,RMVar_hsa_circ_103660,RMVar_hsa_circ_303697,RMVar_hsa_circ_323515,RMVar_hsa_circ_93239,RMVar_hsa_circ_247111,RMVar_hsa_circ_65218,RMVar_hsa_circ_247110 18676 RMVar_ID_18676 Human_SNP_ID_332684068 A-to-I Human chr7 + 100551626 100551626 100551626 GGAAAATAGGCCAGGCAAGGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCTGAGGTGGGC GGAAAATAGGCCAGGCAAGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGC A G AGFG2 Ensembl:ENSG00000106351 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs959265392 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73175,RMVar_hsa_circ_247109,RMVar_hsa_circ_103660,RMVar_hsa_circ_303697,RMVar_hsa_circ_93239,RMVar_hsa_circ_52927,RMVar_hsa_circ_247111,RMVar_hsa_circ_65218 18677 RMVar_ID_18677 Human_SNP_ID_332685352 A-to-I Human chr7 + 100557033 100557033 100557033 AAGCCTGGCCAACATGGTGAAACACCGTCTCTACTCAAAATACAAAAATTAGCTGGGCATGGTGG AAGCCTGGCCAACATGGTGAAACACCGTCTCTGCTCAAAATACAAAAATTAGCTGGGCATGGTGG A G AGFG2 Ensembl:ENSG00000106351 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs966199292 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93239,RMVar_hsa_circ_247113,RMVar_hsa_circ_247111,RMVar_hsa_circ_65218,RMVar_hsa_circ_361739,RMVar_hsa_circ_112166,RMVar_hsa_circ_103614,RMVar_hsa_circ_247114 18678 RMVar_ID_18678 Human_SNP_ID_332685708 A-to-I Human chr7 + 100558603 100558603 100558603 TCACTCTGTCACCCAGGCTGGGGTGTAGTGGCACAATCTCGGCTCACTGCAAACTCCGCCTCTCG TCACTCTGTCACCCAGGCTGGGGTGTAGTGGCGCAATCTCGGCTCACTGCAAACTCCGCCTCTCG A G AGFG2 Ensembl:ENSG00000106351 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs28522285 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16272240 RMVar_hsa_circ_93239,RMVar_hsa_circ_247113,RMVar_hsa_circ_247111,RMVar_hsa_circ_65218,RMVar_hsa_circ_361739,RMVar_hsa_circ_112166,RMVar_hsa_circ_103614,RMVar_hsa_circ_247114 18679 RMVar_ID_18679 Human_SNP_ID_332685709 A-to-I Human chr7 + 100558605 100558605 100558605 ACTCTGTCACCCAGGCTGGGGTGTAGTGGCACAATCTCGGCTCACTGCAAACTCCGCCTCTCGGG ACTCTGTCACCCAGGCTGGGGTGTAGTGGCACCATCTCGGCTCACTGCAAACTCCGCCTCTCGGG A C AGFG2 Ensembl:ENSG00000106351 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1212565940 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93239,RMVar_hsa_circ_247113,RMVar_hsa_circ_247111,RMVar_hsa_circ_65218,RMVar_hsa_circ_361739,RMVar_hsa_circ_112166,RMVar_hsa_circ_103614,RMVar_hsa_circ_247114 18680 RMVar_ID_18680 Human_SNP_ID_332686063 A-to-I Human chr7 + 100560278 100560278 100560278 TTGGCTCACTGCAATCTTCCTCTTCCAGGTTCAAGTGATTCTGGTGCCTCAGCCTCCCGTGTAGT TTGGCTCACTGCAATCTTCCTCTTCCAGGTTCGAGTGATTCTGGTGCCTCAGCCTCCCGTGTAGT A G AGFG2 Ensembl:ENSG00000106351 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs933998232 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93239,RMVar_hsa_circ_247113,RMVar_hsa_circ_247111,RMVar_hsa_circ_65218,RMVar_hsa_circ_361739,RMVar_hsa_circ_112166,RMVar_hsa_circ_103614,RMVar_hsa_circ_247114 18681 RMVar_ID_18681 Human_SNP_ID_332686079 A-to-I Human chr7 + 100560359 100560359 100560359 CACCACCACGCCCAGCTTATTTTTGTGCTTTTAGTAGAGACAGGGTTTTGCCATGTTGGCCAGGC CACCACCACGCCCAGCTTATTTTTGTGCTTTTGGTAGAGACAGGGTTTTGCCATGTTGGCCAGGC A G AGFG2 Ensembl:ENSG00000106351 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs190129851 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93239,RMVar_hsa_circ_247113,RMVar_hsa_circ_247111,RMVar_hsa_circ_65218,RMVar_hsa_circ_361739,RMVar_hsa_circ_112166,RMVar_hsa_circ_103614,RMVar_hsa_circ_247114 18682 RMVar_ID_18682 Human_SNP_ID_332686329 A-to-I Human chr7 + 100561307 100561307 100561307 TGCCACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCAAGGG TGCCACCATGCCTGGCTAATTTTTGTATTTTTGGTAGAGACAGGGTTTCACCATGTTGGCAAGGG A G AGFG2 Ensembl:ENSG00000106351 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1229555651 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93239,RMVar_hsa_circ_247113,RMVar_hsa_circ_247111,RMVar_hsa_circ_65218,RMVar_hsa_circ_361739,RMVar_hsa_circ_112166,RMVar_hsa_circ_103614,RMVar_hsa_circ_247114 18683 RMVar_ID_18683 Human_SNP_ID_332705949 A-to-I Human chr7 - 100625712 100625712 100625712 CCCGGCTAAATTTTTCTATTTTTTGTAGAGACAGGGTTTTACCATGTTGCCCAGGCTGGTCTCAA CCCGGCTAAATTTTTCTATTTTTTGTAGAGACTGGGTTTTACCATGTTGCCCAGGCTGGTCTCAA T A TFR2 Ensembl:ENSG00000106327 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs954372309 Functional Loss SNV dbSNP153 33..33 33 - - - 18684 RMVar_ID_18684 Human_SNP_ID_332711443 A-to-I Human chr7 - 100644048 100644048 100644048 TAAAAATACAAAAATTAGCCGGGCGTGTTGGCACGCGCCTGTAATCCCAGCTACCCAGCAGGCTG TAAAAATACAAAAATTAGCCGGGCGTGTTGGCGCGCGCCTGTAATCCCAGCTACCCAGCAGGCTG T C ACTL6B Ensembl:ENSG00000077080 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1393112374 Functional Loss SNV dbSNP153 33..33 33 - - - 18685 RMVar_ID_18685 Human_SNP_ID_332764505 A-to-I Human chr7 - 100816916 100816916 100816916 ACCGCGCCTGGCCGATTTTTTGTATTTTTAGTAGAGACGGGGCTTCACCGCGTTGGCCAGGCTGG ACCGCGCCTGGCCGATTTTTTGTATTTTTAGTGGAGACGGGGCTTCACCGCGTTGGCCAGGCTGG T C EPHB4 Ensembl:ENSG00000196411 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1164645358 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13997,RMVar_hsa_circ_88378,RMVar_hsa_circ_247162,RMVar_hsa_circ_48921,RMVar_hsa_circ_98542,RMVar_hsa_circ_88198,RMVar_hsa_circ_247170,RMVar_hsa_circ_247171,RMVar_hsa_circ_125694,RMVar_hsa_circ_102547,RMVar_hsa_circ_88897,RMVar_hsa_circ_247173,RMVar_hsa_circ_247174,RMVar_hsa_circ_98489,RMVar_hsa_circ_247175,RMVar_hsa_circ_247176 18686 RMVar_ID_18686 Human_SNP_ID_332766580 A-to-I Human chr7 - 100822594 100822593 100822595 TGGGGCCGAGGCCACCGGGAAGGTGAATGTCAAGACGCTGCGTCTGGGACCGCTCAGCAAGGCTG TGGGGCCGAGGCCACCGGGAAGGTGAATGTC__GACGCTGCGTCTGGGACCGCTCAGCAAGGCTG CTT C EPHB4 Ensembl:ENSG00000196411 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1562973705 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_7666576 Human_Splice_Rec_901058,Human_Splice_Rec_901088,Human_Splice_Rec_901114,Human_Splice_Rec_901144,Human_Splice_Rec_901192,Human_Splice_Rec_901208 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 18687 RMVar_ID_18687 Human_SNP_ID_332766581 A-to-I Human chr7 - 100822594 100822594 100822594 TGGGGCCGAGGCCACCGGGAAGGTGAATGTCAAGACGCTGCGTCTGGGACCGCTCAGCAAGGCTG TGGGGCCGAGGCCACCGGGAAGGTGAATGTCAGGACGCTGCGTCTGGGACCGCTCAGCAAGGCTG T C EPHB4 Ensembl:ENSG00000196411 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs17854760 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7666576 Human_Splice_Rec_901058,Human_Splice_Rec_901088,Human_Splice_Rec_901114,Human_Splice_Rec_901144,Human_Splice_Rec_901192,Human_Splice_Rec_901208 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 18688 RMVar_ID_18688 Human_SNP_ID_332769263 A-to-I Human chr7 - 100830240 100830240 100830240 TCAAGCAATTCTCCTGTCTCAGCCTCCCGAGTAGCTGGGACTGCAGGCCTGCACCACCACACCTG TCAAGCAATTCTCCTGTCTCAGCCTCCCGAGTGGCTGGGACTGCAGGCCTGCACCACCACACCTG T C RF00017-4590,SLC12A9-AS1,SLC12A9-AS1:2 RNACentral:URS0000965567,RNACentral:URS0000D59401,RNACentral:URS0000D56D32 SRP RNA,lincRNA,lincRNA intron,exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs796527810 Functional Loss SNV dbSNP153 33..33 33 - - - 18689 RMVar_ID_18689 Human_SNP_ID_332774027 A-to-I Human chr7 + 100848447 100848446 100848447 TTGAGCCTGGGAGATAGAGGTTGCTGTGAGCTATGATGGTGCCACTGTACTCCAGCCTAGGCGAC TTGAGCCTGGGAGATAGAGGTTGCTGTGAGCT_TGATGGTGCCACTGTACTCCAGCCTAGGCGAC TA T SLC12A9 Ensembl:ENSG00000146828 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1484206863 Functional Loss DEL dbSNP153 33..33 33 - - - 18690 RMVar_ID_18690 Human_SNP_ID_332774028 A-to-I Human chr7 + 100848447 100848447 100848447 TTGAGCCTGGGAGATAGAGGTTGCTGTGAGCTATGATGGTGCCACTGTACTCCAGCCTAGGCGAC TTGAGCCTGGGAGATAGAGGTTGCTGTGAGCTGTGATGGTGCCACTGTACTCCAGCCTAGGCGAC A G SLC12A9 Ensembl:ENSG00000146828 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1275778827 Functional Loss SNV dbSNP153 33..33 33 - - - 18691 RMVar_ID_18691 Human_SNP_ID_332775967 A-to-I Human chr7 + 100855033 100855033 100855033 TAAAATTACAAAAATTAGCTGGGCATGATGGCACCCGCCTGTGATTCCAGCTACTCGGGAGGCTG TAAAATTACAAAAATTAGCTGGGCATGATGGCCCCCGCCTGTGATTCCAGCTACTCGGGAGGCTG A C SLC12A9 Ensembl:ENSG00000146828 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs920747244 Functional Loss SNV dbSNP153 33..33 33 - - - 18692 RMVar_ID_18692 Human_SNP_ID_332776011 A-to-I Human chr7 + 100855197 100855197 100855197 CAGGCTGCAGTGCAGTGGCGCCATCATAGCTCACTGTGATCTCGACTTCCTGGGCTCAAGTGATC CAGGCTGCAGTGCAGTGGCGCCATCATAGCTCCCTGTGATCTCGACTTCCTGGGCTCAAGTGATC A C SLC12A9 Ensembl:ENSG00000146828 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs186131060 Functional Loss SNV dbSNP153 33..33 33 - - - 18693 RMVar_ID_18693 Human_SNP_ID_332776267 A-to-I Human chr7 + 100856217 100856217 100856217 ACAGTTGGGGCTGGGTCCCTTCTTATTTATTTATTTATTTTGAGATGGAGTCTTGCTTTGTTGCC ACAGTTGGGGCTGGGTCCCTTCTTATTTATTTGTTTATTTTGAGATGGAGTCTTGCTTTGTTGCC A G SLC12A9 Ensembl:ENSG00000146828 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1423931462 Functional Loss SNV dbSNP153 33..33 33 - - - 18694 RMVar_ID_18694 Human_SNP_ID_332776366 A-to-I Human chr7 + 100856557 100856557 100856557 TTTTTCTTGAGAGAAGGTCTCACTCTGTCACCAAGGCTGGAGTGCAGTGGTACCATCTCGGCTCA TTTTTCTTGAGAGAAGGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGTACCATCTCGGCTCA A C SLC12A9 Ensembl:ENSG00000146828 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1330686207 Functional Loss SNV dbSNP153 33..33 33 - - - 18695 RMVar_ID_18695 Human_SNP_ID_332776375 A-to-I Human chr7 + 100856594 100856594 100856594 TGGAGTGCAGTGGTACCATCTCGGCTCAATGCAACTTCTGCCTCCCGGGCTCATGCGATTCTCCC TGGAGTGCAGTGGTACCATCTCGGCTCAATGCGACTTCTGCCTCCCGGGCTCATGCGATTCTCCC A G SLC12A9 Ensembl:ENSG00000146828 Protein coding intron GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-Seq:(High) rs997553905 Functional Loss SNV dbSNP153 33..33 33 - - - 18696 RMVar_ID_18696 Human_SNP_ID_332780612 A-to-I Human chr7 + 100869917 100869917 100869917 GTTATAATAATAATAGAATATATAGTATATATAATTGTTTCGGTATATATTACAATGTATATTAC GTTATAATAATAATAGAATATATAGTATATATCATTGTTTCGGTATATATTACAATGTATATTAC A C TRIP6 Ensembl:ENSG00000087077 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1013451749 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81204,RMVar_hsa_circ_110564,RMVar_hsa_circ_247190,RMVar_hsa_circ_118310,RMVar_hsa_circ_247191,RMVar_hsa_circ_247192 18697 RMVar_ID_18697 Human_SNP_ID_332783312 A-to-I Human chr7 + 100877687 100877687 100877687 GGGATTACAGGTGCGTGCCACTCTGCCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCA GGGATTACAGGTGCGTGCCACTCTGCCTGGCTCATTTTTGTATTTTTAGTAGAGATGGGGTTTCA A C SRRT Ensembl:ENSG00000087087 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1235625632 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103373,RMVar_hsa_circ_111923,RMVar_hsa_circ_247196,RMVar_hsa_circ_247197 18698 RMVar_ID_18698 Human_SNP_ID_332783746 A-to-I Human chr7 + 100879060 100879060 100879060 CACTGTAACCTCCATCTTCCGGGTTCAAAACGATTCTCCCACCTCAGCCTCCCGAGTAGTTGGGA CACTGTAACCTCCATCTTCCGGGTTCAAAACGGTTCTCCCACCTCAGCCTCCCGAGTAGTTGGGA A G SRRT Ensembl:ENSG00000087087 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1310634505 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103373,RMVar_hsa_circ_111923,RMVar_hsa_circ_247196,RMVar_hsa_circ_247197 18699 RMVar_ID_18699 Human_SNP_ID_332783932 A-to-I Human chr7 + 100879733 100879733 100879733 AAGGGGCTGAGGCAGGAGAATTGCTTGAGCCCAGGAGGCGGAGGCTGTAGTGAGCCGAGAGTGAT AAGGGGCTGAGGCAGGAGAATTGCTTGAGCCCGGGAGGCGGAGGCTGTAGTGAGCCGAGAGTGAT A G SRRT Ensembl:ENSG00000087087 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1282103032 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103373,RMVar_hsa_circ_111923,RMVar_hsa_circ_247196,RMVar_hsa_circ_247197 18700 RMVar_ID_18700 Human_SNP_ID_332857527 A-to-I Human chr7 + 101091477 101091477 101091477 CGCCAGGCACGGTGACTCAAGCCTGTAATCCCAGCACTCTGGGAGGCTGGGGTGGGTGGATCACT CGCCAGGCACGGTGACTCAAGCCTGTAATCCCGGCACTCTGGGAGGCTGGGGTGGGTGGATCACT A G TRIM56 Ensembl:ENSG00000169871 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs939176272 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2774351 RMVar_hsa_circ_127182,RMVar_hsa_circ_247213 18701 RMVar_ID_18701 Human_SNP_ID_332857536 A-to-I Human chr7 + 101091507 101091507 101091507 CCAGCACTCTGGGAGGCTGGGGTGGGTGGATCACTCAAGGTCAGGAGTTCGAGACCAGCCTGGCC CCAGCACTCTGGGAGGCTGGGGTGGGTGGATCCCTCAAGGTCAGGAGTTCGAGACCAGCCTGGCC A C TRIM56 Ensembl:ENSG00000169871 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs551083974 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26051838 RMVar_hsa_circ_127182,RMVar_hsa_circ_247213 18702 RMVar_ID_18702 Human_SNP_ID_332857540 A-to-I Human chr7 + 101091517 101091517 101091517 GGGAGGCTGGGGTGGGTGGATCACTCAAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGAGA GGGAGGCTGGGGTGGGTGGATCACTCAAGGTCGGGAGTTCGAGACCAGCCTGGCCAACATGGAGA A G TRIM56 Ensembl:ENSG00000169871 Protein coding 3'UTR GSE38233;GSE99789;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29796672,31158229,32596459,32596459 RNA-Seq:(High) rs1446810197 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127182,RMVar_hsa_circ_247213 18703 RMVar_ID_18703 Human_SNP_ID_332857547 A-to-I Human chr7 + 101091568 101091568 101091568 GGCCAACATGGAGAAACCCCATCTCTACTAAAAATACAAAAATTAGCTAGGCGTGGGAGCGGGCG GGCCAACATGGAGAAACCCCATCTCTACTAAAGATACAAAAATTAGCTAGGCGTGGGAGCGGGCG A G TRIM56 Ensembl:ENSG00000169871 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs892541232 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127182,RMVar_hsa_circ_247213 18704 RMVar_ID_18704 Human_SNP_ID_332859113 A-to-I Human chr7 + 101096068 101096068 101096068 AAAATTAGCCAGGCGTGGTGGCACATGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGTGGGAGA AAAATTAGCCAGGCGTGGTGGCACATGCCTGTGATCCCAGCTACTCAGGAGGCTGAGGTGGGAGA A G TRIM56 Ensembl:ENSG00000169871 Protein coding 3'UTR GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs555964263 Functional Loss SNV dbSNP153 33..33 33 - - - 18705 RMVar_ID_18705 Human_SNP_ID_332894253 A-to-I Human chr7 - 101213855 101213855 101213855 GTCTCTACTAAAAACACAAAAATTAGCCGGGCATGGTGGTGCGCGCCTGTAATCCTGGCTACCCG GTCTCTACTAAAAACACAAAAATTAGCCGGGCGTGGTGGTGCGCGCCTGTAATCCTGGCTACCCG T C PLOD3 Ensembl:ENSG00000106397 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs952546325 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75974,RMVar_hsa_circ_247241 18706 RMVar_ID_18706 Human_SNP_ID_332901997 A-to-I Human chr7 - 101239851 101239851 101239851 ATCGTGGGAGGCATGGCCCTGGGTGTGGCGGGACTGGCCGGACTCATCGGACTTGCTGTGTCCAA ATCGTGGGAGGCATGGCCCTGGGTGTGGCGGGGCTGGCCGGACTCATCGGACTTGCTGTGTCCAA T C FIS1 Ensembl:ENSG00000214253 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs867624477 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14508,Human_RBP_ID_671745,Human_RBP_ID_844275,Human_RBP_ID_1049564,Human_RBP_ID_3972318,Human_RBP_ID_5123337,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 18707 RMVar_ID_18707 Human_SNP_ID_332902738 A-to-I Human chr7 - 101242100 101242100 101242100 CTGTCTGTGTAACAAAGATGTTTAAATTAGCCAGGCATGGTGGTGTGTGCTTATAGTCCCAGCTA CTGTCTGTGTAACAAAGATGTTTAAATTAGCCGGGCATGGTGGTGTGTGCTTATAGTCCCAGCTA T C FIS1 Ensembl:ENSG00000214253 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1220951853 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89647,RMVar_hsa_circ_80094,RMVar_hsa_circ_247250,RMVar_hsa_circ_247251 18708 RMVar_ID_18708 Human_SNP_ID_332902740 A-to-I Human chr7 - 101242104 101242104 101242104 TGGCCTGTCTGTGTAACAAAGATGTTTAAATTAGCCAGGCATGGTGGTGTGTGCTTATAGTCCCA TGGCCTGTCTGTGTAACAAAGATGTTTAAATTGGCCAGGCATGGTGGTGTGTGCTTATAGTCCCA T C FIS1 Ensembl:ENSG00000214253 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1251212507 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89647,RMVar_hsa_circ_80094,RMVar_hsa_circ_247250,RMVar_hsa_circ_247251 18709 RMVar_ID_18709 Human_SNP_ID_332903856 A-to-I Human chr7 - 101245629 101245629 101245629 TCAAGCGATCCTCCTGCCTCAGCCGCCCCAGTAGCTGGGAGTACAGGTGCACGCCACCACGCCGG TCAAGCGATCCTCCTGCCTCAGCCGCCCCAGTTGCTGGGAGTACAGGTGCACGCCACCACGCCGG T A FIS1 Ensembl:ENSG00000214253 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1250506374 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80094,RMVar_hsa_circ_247251 18710 RMVar_ID_18710 Human_SNP_ID_332903858 A-to-I Human chr7 - 101245641 101245641 101245641 GAACTCCCGGACTCAAGCGATCCTCCTGCCTCAGCCGCCCCAGTAGCTGGGAGTACAGGTGCACG GAACTCCCGGACTCAAGCGATCCTCCTGCCTCGGCCGCCCCAGTAGCTGGGAGTACAGGTGCACG T C FIS1 Ensembl:ENSG00000214253 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1340716237 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80094,RMVar_hsa_circ_247251 18711 RMVar_ID_18711 Human_SNP_ID_332904039 A-to-I Human chr7 - 101246461 101246461 101246461 AAAACAACCTGGGTGTGGTGGTGCACACCTGTAGTCCCAGCTTCTTGGGAGACTAAGGCAGGAGG AAAACAACCTGGGTGTGGTGGTGCACACCTGTGGTCCCAGCTTCTTGGGAGACTAAGGCAGGAGG T C FIS1 Ensembl:ENSG00000214253 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1373728460 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80094,RMVar_hsa_circ_247251 18712 RMVar_ID_18712 Human_SNP_ID_332904088 A-to-I Human chr7 - 101246662 101246658 101246662 AAAACCCCATCTCTGCTAAAAATACAAAAATTAGCTGGGTGTGATGGCCGGCGCCTGTAATCCCA AAAACCCCATCTCTGCTAAAAATACAAAAATT____GGGTGTGATGGCCGGCGCCTGTAATCCCA CAGCT C FIS1 Ensembl:ENSG00000214253 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1228507546 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_80094,RMVar_hsa_circ_247251 18713 RMVar_ID_18713 Human_SNP_ID_332904929 A-to-I Human chr7 - 101249285 101249285 101249285 GACACCTGTAATCCCAGGACTTTGAGAGGCCAAGGCGGGCGGATTGCTTGAGCTCAGGAGTTCCA GACACCTGTAATCCCAGGACTTTGAGAGGCCACGGCGGGCGGATTGCTTGAGCTCAGGAGTTCCA T G FIS1 Ensembl:ENSG00000214253 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053887878 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80094,RMVar_hsa_circ_247251 18714 RMVar_ID_18714 Human_SNP_ID_332922518 A-to-I Human chr7 - 101311777 101311777 101311777 TTGAACTCCTGACCTTGTGGTCTACCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG TTGAACTCCTGACCTTGTGGTCTACCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG T C IFT22 Ensembl:ENSG00000128581 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037431141 Functional Loss SNV dbSNP153 33..33 33 - - - 18715 RMVar_ID_18715 Human_SNP_ID_332922912 A-to-I Human chr7 - 101312985 101312985 101312985 TACTAAAAATACAAAAATTAGCTGGGCGTGGTAGCACGTGCCTGTAATCCCAGCTACCTGGGAAG TACTAAAAATACAAAAATTAGCTGGGCGTGGTTGCACGTGCCTGTAATCCCAGCTACCTGGGAAG T A IFT22 Ensembl:ENSG00000128581 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1433973343 Functional Loss SNV dbSNP153 33..33 33 - - - 18716 RMVar_ID_18716 Human_SNP_ID_332922966 A-to-I Human chr7 - 101313204 101313204 101313204 CCCCATCTCTACTAAAAATACAAAAATTCGCCAGGCATGTTGGCACACACCTGTAATACCAGCTA CCCCATCTCTACTAAAAATACAAAAATTCGCCGGGCATGTTGGCACACACCTGTAATACCAGCTA T C IFT22 Ensembl:ENSG00000128581 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs919299073 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22514933 18717 RMVar_ID_18717 Human_SNP_ID_332923198 A-to-I Human chr7 - 101313995 101313995 101313995 AAAATTCACAGGGTGTGTTGGCACACGCCTGTAATACCAGCTACTCAGGTGGCTGAGGCATAAGA AAAATTCACAGGGTGTGTTGGCACACGCCTGTGATACCAGCTACTCAGGTGGCTGAGGCATAAGA T C IFT22 Ensembl:ENSG00000128581 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1416086153 Functional Loss SNV dbSNP153 33..33 33 - - - 18718 RMVar_ID_18718 Human_SNP_ID_332923247 A-to-I Human chr7 - 101314152 101314151 101314153 ACTCCATCTCAAAAAAAAAAGAGTTCTAGCCCAGGAGCGGTGGCTCACACTTGTAATCCCAGCAC ACTCCATCTCAAAAAAAAAAGAGTTCTAGCC__GGAGCGGTGGCTCACACTTGTAATCCCAGCAC CTG C IFT22 Ensembl:ENSG00000128581 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1392419076 Functional Loss DEL dbSNP153 32..33 33 - - - 18719 RMVar_ID_18719 Human_SNP_ID_332923290 A-to-I Human chr7 - 101314294 101314293 101314294 AAATCAGCTGGGTGTGGTGCCGCGTGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCATAAGAA AAATCAGCTGGGTGTGGTGCCGCGTGCCTGTA_TCCCAGCTACTTGGGAGGCTGAGGCATAAGAA AT A IFT22 Ensembl:ENSG00000128581 Protein coding 3'UTR GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1047878163 Functional Loss DEL dbSNP153 33..33 33 - - - 18720 RMVar_ID_18720 Human_SNP_ID_332923291 A-to-I Human chr7 - 101314294 101314294 101314294 AAATCAGCTGGGTGTGGTGCCGCGTGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCATAAGAA AAATCAGCTGGGTGTGGTGCCGCGTGCCTGTATTCCCAGCTACTTGGGAGGCTGAGGCATAAGAA T A IFT22 Ensembl:ENSG00000128581 Protein coding 3'UTR GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1293776685 Functional Loss SNV dbSNP153 33..33 33 - - - 18721 RMVar_ID_18721 Human_SNP_ID_332923299 A-to-I Human chr7 - 101314339 101314339 101314339 CATCCTGACCAACGTGGTGAAACCCCATCTCTACTAAAAATAGAAAAATCAGCTGGGTGTGGTGC CATCCTGACCAACGTGGTGAAACCCCATCTCTTCTAAAAATAGAAAAATCAGCTGGGTGTGGTGC T A IFT22 Ensembl:ENSG00000128581 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924374105 Functional Loss SNV dbSNP153 33..33 33 - - - 18722 RMVar_ID_18722 Human_SNP_ID_333006890 A-to-I Human chr7 - 101623917 101623916 101623917 TCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGGTGGGATTGCAGGCACGCACCACCATGCCCA TCAAGCAATTCTCCTGCCTCAGCCTCCCAAGT_GGTGGGATTGCAGGCACGCACCACCATGCCCA CT C MYL10 Ensembl:ENSG00000106436 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1554353203 Functional Loss DEL dbSNP153 33..33 33 - - - 18723 RMVar_ID_18723 Human_SNP_ID_333058360 A-to-I Human chr7 + 101822778 101822778 101822778 CAAAAATTAGCCTGGCGTGGTGGCGCATATCCATAATCCCAGATACTCGGCAGGCTGAGGCATGA CAAAAATTAGCCTGGCGTGGTGGCGCATATCCGTAATCCCAGATACTCGGCAGGCTGAGGCATGA A G CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1352264296 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3030884,Human_RBP_ID_15947283,Human_RBP_ID_26051970 18724 RMVar_ID_18724 Human_SNP_ID_333058374 A-to-I Human chr7 + 101822826 101822826 101822826 GGCAGGCTGAGGCATGAGAATTGCTTGAGCCCAGGAGGTGGAGGTTGCAGTGAGCTGAGATCGTG GGCAGGCTGAGGCATGAGAATTGCTTGAGCCCGGGAGGTGGAGGTTGCAGTGAGCTGAGATCGTG A G CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1362336714 Functional Loss SNV dbSNP153 33..33 33 - - - 18725 RMVar_ID_18725 Human_SNP_ID_333058377 A-to-I Human chr7 + 101822842 101822842 101822842 AGAATTGCTTGAGCCCAGGAGGTGGAGGTTGCAGTGAGCTGAGATCGTGTGACTGCTCTGCATGC AGAATTGCTTGAGCCCAGGAGGTGGAGGTTGCGGTGAGCTGAGATCGTGTGACTGCTCTGCATGC A G CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1275956057 Functional Loss SNV dbSNP153 33..33 33 - - - 18726 RMVar_ID_18726 Human_SNP_ID_333061643 A-to-I Human chr7 + 101834902 101834902 101834902 CTTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCTCTTGAACCCGGGAGGCAGAGGTT CTTGTAATCCCAGCTACTCAGGAGGCTGAGGCGGGAGAATCTCTTGAACCCGGGAGGCAGAGGTT A G CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1436806025 Functional Loss SNV dbSNP153 33..33 33 - - - 18727 RMVar_ID_18727 Human_SNP_ID_333064317 A-to-I Human chr7 + 101845186 101845186 101845186 CTCTCTTTTTGAAATGGAGATGGGGTCTCACTATGTTGCCCACTCTGGTCTCAAACTCCTGGGCT CTCTCTTTTTGAAATGGAGATGGGGTCTCACTGTGTTGCCCACTCTGGTCTCAAACTCCTGGGCT A G CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs771254017 Functional Loss SNV dbSNP153 33..33 33 - - - 18728 RMVar_ID_18728 Human_SNP_ID_333065692 A-to-I Human chr7 + 101850586 101850586 101850586 TATTTTTTGTAGAGATGGCATCTCACCATGTTACCCAGGTGGTCTCGAACTCCTGGGCTCAAGCA TATTTTTTGTAGAGATGGCATCTCACCATGTTCCCCAGGTGGTCTCGAACTCCTGGGCTCAAGCA A C CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs995176486 Functional Loss SNV dbSNP153 33..33 33 - - - 18729 RMVar_ID_18729 Human_SNP_ID_333070152 A-to-I Human chr7 + 101867987 101867987 101867987 CCCGCCTTGGCCTCCTAAAGTGCTGGGATTACAAGTATGAGCCACTGTGCCTGGCCTCTCTTTTT CCCGCCTTGGCCTCCTAAAGTGCTGGGATTACCAGTATGAGCCACTGTGCCTGGCCTCTCTTTTT A C CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1196937541 Functional Loss SNV dbSNP153 33..33 33 - - - 18730 RMVar_ID_18730 Human_SNP_ID_333071183 A-to-I Human chr7 + 101871762 101871762 101871762 TTTGTGGGCCGGGTGCCGTGGCTCTCGCCTGTAATCCCAGTTCTTTGGGAGGCCAAGGCGGGTGG TTTGTGGGCCGGGTGCCGTGGCTCTCGCCTGTGATCCCAGTTCTTTGGGAGGCCAAGGCGGGTGG A G CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs537993530 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15948797 18731 RMVar_ID_18731 Human_SNP_ID_333071184 A-to-I Human chr7 + 101871762 101871762 101871762 TTTGTGGGCCGGGTGCCGTGGCTCTCGCCTGTAATCCCAGTTCTTTGGGAGGCCAAGGCGGGTGG TTTGTGGGCCGGGTGCCGTGGCTCTCGCCTGTTATCCCAGTTCTTTGGGAGGCCAAGGCGGGTGG A T CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs537993530 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15948797 18732 RMVar_ID_18732 Human_SNP_ID_333078012 A-to-I Human chr7 + 101899477 101899477 101899477 GGGAGGCTGAGACAGGAGAATCTCTTGAACCCAGGAGGCAGAGGTTGCAGTGAGTCAAGATTGGA GGGAGGCTGAGACAGGAGAATCTCTTGAACCCGGGAGGCAGAGGTTGCAGTGAGTCAAGATTGGA A G CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1238185084 Functional Loss SNV dbSNP153 33..33 33 - - - 18733 RMVar_ID_18733 Human_SNP_ID_333085051 A-to-I Human chr7 + 101927508 101927508 101927508 AGCGAGACCCCATCTCTACAAAAAAATGAAGAAATTAGCCGGGCGTGGTGGTGCATACCTGTAAT AGCGAGACCCCATCTCTACAAAAAAATGAAGATATTAGCCGGGCGTGGTGGTGCATACCTGTAAT A T CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947358288 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7667355 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 18734 RMVar_ID_18734 Human_SNP_ID_333086101 A-to-I Human chr7 + 101931738 101931738 101931738 GGCATGCACCATGGTGTCTGACTGATTTTTGTATTTGTTGTAGGGAGGGGTTCTCACTATGTTAC GGCATGCACCATGGTGTCTGACTGATTTTTGTGTTTGTTGTAGGGAGGGGTTCTCACTATGTTAC A G CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs565077872 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3032059,Human_RBP_ID_15949799 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 18735 RMVar_ID_18735 Human_SNP_ID_333086106 A-to-I Human chr7 + 101931764 101931764 101931764 TTTTGTATTTGTTGTAGGGAGGGGTTCTCACTATGTTACGCACGCTGGTCTCAAACTCCTGGGCT TTTTGTATTTGTTGTAGGGAGGGGTTCTCACTGTGTTACGCACGCTGGTCTCAAACTCCTGGGCT A G CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1381103307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3032061,Human_RBP_ID_15949800 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 18736 RMVar_ID_18736 Human_SNP_ID_333090281 A-to-I Human chr7 + 101949155 101949154 101949156 GGTCATTATTATTATTATTATTATTTTGAGACAGAGTCTCACTCTGTCGCCCAGGCTGGAGTGCA GGTCATTATTATTATTATTATTATTTTGAGAC__AGTCTCACTCTGTCGCCCAGGCTGGAGTGCA CAG C CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350424839 Functional Loss DEL dbSNP153 33..34 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 18737 RMVar_ID_18737 Human_SNP_ID_333090659 A-to-I Human chr7 + 101950579 101950579 101950579 TTTTCATCATTCCATAACTCACCTCCATAAATAAAGTTTTATTGGCACTCAGCCATACTCATTTG TTTTCATCATTCCATAACTCACCTCCATAAATGAAGTTTTATTGGCACTCAGCCATACTCATTTG A G CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1400930260 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 18738 RMVar_ID_18738 Human_SNP_ID_333091013 A-to-I Human chr7 + 101952126 101952126 101952126 ATTGCAGATTCTGACCAGGCGTAGTGGCTCACACCTATAATCCCAATACTTTGAGAGGCCAAGGT ATTGCAGATTCTGACCAGGCGTAGTGGCTCACGCCTATAATCCCAATACTTTGAGAGGCCAAGGT A G CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1466722323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_175688 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 18739 RMVar_ID_18739 Human_SNP_ID_333092718 A-to-I Human chr7 + 101958967 101958967 101958967 GCCTCGACCTCCCTGGCTTAAGCAATCCTCCCACCTCAGCCCTCCTAAGTAGCTAGGACTACAGG GCCTCGACCTCCCTGGCTTAAGCAATCCTCCCGCCTCAGCCCTCCTAAGTAGCTAGGACTACAGG A G CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1013855180 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 18740 RMVar_ID_18740 Human_SNP_ID_333092740 A-to-I Human chr7 + 101959094 101959094 101959094 GTTGCCTAAGCTGGTCTCAAATTCCTGGGCTTAAGTGATCCGCCCACTTCGGCCTCCCAAAGGAT GTTGCCTAAGCTGGTCTCAAATTCCTGGGCTTGAGTGATCCGCCCACTTCGGCCTCCCAAAGGAT A G CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1001741915 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3032299 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 18741 RMVar_ID_18741 Human_SNP_ID_333095242 A-to-I Human chr7 + 101969228 101969228 101969228 GTGGTGGCGCACACCTGTACTTTCAGCTACCCAGGAGGCTGAGGTGGGAGGATTGCTTGAGCCTG GTGGTGGCGCACACCTGTACTTTCAGCTACCCGGGAGGCTGAGGTGGGAGGATTGCTTGAGCCTG A G CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1304998725 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 18742 RMVar_ID_18742 Human_SNP_ID_333102750 A-to-I Human chr7 + 101997564 101997564 101997564 CGGGGTTTCACCAGGTTGGTCAGGCTGGTCTCAAACTTCTGAACTCAAATGATCCTCCCGCCTCA CGGGGTTTCACCAGGTTGGTCAGGCTGGTCTCGAACTTCTGAACTCAAATGATCCTCCCGCCTCA A G CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1247045596 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3032564 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 18743 RMVar_ID_18743 Human_SNP_ID_333102751 A-to-I Human chr7 + 101997564 101997564 101997564 CGGGGTTTCACCAGGTTGGTCAGGCTGGTCTCAAACTTCTGAACTCAAATGATCCTCCCGCCTCA CGGGGTTTCACCAGGTTGGTCAGGCTGGTCTCTAACTTCTGAACTCAAATGATCCTCCCGCCTCA A T CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1247045596 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3032564 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 18744 RMVar_ID_18744 Human_SNP_ID_333106339 A-to-I Human chr7 + 102011934 102011934 102011934 GGGTTCAAGTGATTCTCCAACCTCAGCCTCCCAAGTAGCTAGGATTACAGGCGCCCATCACCACA GGGTTCAAGTGATTCTCCAACCTCAGCCTCCCGAGTAGCTAGGATTACAGGCGCCCATCACCACA A G CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1563128011 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 18745 RMVar_ID_18745 Human_SNP_ID_333106344 A-to-I Human chr7 + 102011974 102011974 102011974 AGGATTACAGGCGCCCATCACCACACCTGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCA AGGATTACAGGCGCCCATCACCACACCTGGCTGATTTTTGTATTTTTAGTAGAGACGGGGTTTCA A G CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs923176102 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 18746 RMVar_ID_18746 Human_SNP_ID_333106560 A-to-I Human chr7 + 102012811 102012811 102012811 GAATGAAGCAAGCATTCCCCCAGAGAATTCTTAAATCATCTTAGCCGGTCATGGAATTTCCCAGC GAATGAAGCAAGCATTCCCCCAGAGAATTCTTCAATCATCTTAGCCGGTCATGGAATTTCCCAGC A C CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1424396432 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 18747 RMVar_ID_18747 Human_SNP_ID_333111482 A-to-I Human chr7 + 102032065 102032063 102032065 TGCCCACCTCAGCCTCCCAAGTAGCTAGGACCACAGGCTCTTGCCACCATGCCTGCCTAAATTTT TGCCCACCTCAGCCTCCCAAGTAGCTAGGAC__CAGGCTCTTGCCACCATGCCTGCCTAAATTTT CCA C CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264443561 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_16156,RMVar_hsa_circ_304804,RMVar_hsa_circ_352082,RMVar_hsa_circ_307725,RMVar_hsa_circ_296973,RMVar_hsa_circ_304656,RMVar_hsa_circ_247261,RMVar_hsa_circ_351005,RMVar_hsa_circ_363183 18748 RMVar_ID_18748 Human_SNP_ID_333126695 A-to-I Human chr7 + 102092792 102092791 102092792 AAAATTATCCTGGCATGGTCGTGTGCGCCTGCAATCTCAGATACTTGGGAGGCTGAGGCAGGAGA AAAATTATCCTGGCATGGTCGTGTGCGCCTGC_ATCTCAGATACTTGGGAGGCTGAGGCAGGAGA CA C CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1168835005 Functional Loss DEL dbSNP153 33..33 33 - - - 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 18749 RMVar_ID_18749 Human_SNP_ID_333131000 A-to-I Human chr7 + 102108396 102108396 102108396 GAGACAGAGTCTTGCTCTGTCACCCAGGCTGGAATGCAGTCTCACAATCTCAGCTCACTGCAACC GAGACAGAGTCTTGCTCTGTCACCCAGGCTGGGATGCAGTCTCACAATCTCAGCTCACTGCAACC A G CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1195318727 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36611,RMVar_hsa_circ_16156,RMVar_hsa_circ_304804,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_71288,RMVar_hsa_circ_91374,RMVar_hsa_circ_52159,RMVar_hsa_circ_21205,RMVar_hsa_circ_247262,RMVar_hsa_circ_247263,RMVar_hsa_circ_247264,RMVar_hsa_circ_296514,RMVar_hsa_circ_359801,RMVar_hsa_circ_84013,RMVar_hsa_circ_247265,RMVar_hsa_circ_247266,RMVar_hsa_circ_85687,RMVar_hsa_circ_247267 18750 RMVar_ID_18750 Human_SNP_ID_333133938 A-to-I Human chr7 + 102119767 102119767 102119767 CAGGGTCTCACTGTGTTGCCCAGAGTGGTCTCAAACTCCTGGCCTCAGGTGATCCTCCCGTCTTA CAGGGTCTCACTGTGTTGCCCAGAGTGGTCTCGAACTCCTGGCCTCAGGTGATCCTCCCGTCTTA A G CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1554492896 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18872849 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 18751 RMVar_ID_18751 Human_SNP_ID_333134226 A-to-I Human chr7 + 102121007 102121007 102121007 TTCGCTTGAGCCTGGAAGTTCCAGCCTGTAGTAAGCTATGATTGCATCACTGTACTCCAGCCTGA TTCGCTTGAGCCTGGAAGTTCCAGCCTGTAGTGAGCTATGATTGCATCACTGTACTCCAGCCTGA A G CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1563271381 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15951964 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 18752 RMVar_ID_18752 Human_SNP_ID_333137027 A-to-I Human chr7 + 102131028 102131028 102131028 AAAATTAGCCGGGCGTGGTGGTACACGCCTGTAGTCCCAGCTACTCAGAAAGCTGAGTCAGCGAG AAAATTAGCCGGGCGTGGTGGTACACGCCTGTGGTCCCAGCTACTCAGAAAGCTGAGTCAGCGAG A G CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1462444789 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 18753 RMVar_ID_18753 Human_SNP_ID_333145058 A-to-I Human chr7 + 102161710 102161709 102161710 TCAGCTCACTGCATCCTCCACCTCATGGGTTCAGGCAATTCTCCTGCCTCAGCCTCCCAAGTAGC TCAGCTCACTGCATCCTCCACCTCATGGGTTC_GGCAATTCTCCTGCCTCAGCCTCCCAAGTAGC CA C CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1364505729 Functional Loss DEL dbSNP153 33..33 33 - - - 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 18754 RMVar_ID_18754 Human_SNP_ID_333146828 A-to-I Human chr7 + 102168504 102168504 102168504 CCCCATCTCTACTCAAAACACAAAAATTAGCCAGGCATGGTGGGCACCTGTAATTCCAGCTACTC CCCCATCTCTACTCAAAACACAAAAATTAGCCGGGCATGGTGGGCACCTGTAATTCCAGCTACTC A G CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1175059224 Functional Loss SNV dbSNP153 33..33 33 - - - 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 18755 RMVar_ID_18755 Human_SNP_ID_333146829 A-to-I Human chr7 + 102168504 102168504 102168504 CCCCATCTCTACTCAAAACACAAAAATTAGCCAGGCATGGTGGGCACCTGTAATTCCAGCTACTC CCCCATCTCTACTCAAAACACAAAAATTAGCCTGGCATGGTGGGCACCTGTAATTCCAGCTACTC A T CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1175059224 Functional Loss SNV dbSNP153 33..33 33 - - - 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 18756 RMVar_ID_18756 Human_SNP_ID_333147978 A-to-I Human chr7 + 102172209 102172209 102172209 CACCTCCCGGGTTCAAGCAATTCTCGTGCCTCAGCCTCCCAACTAGCTGGAGCTGCAGGCGCATA CACCTCCCGGGTTCAAGCAATTCTCGTGCCTCCGCCTCCCAACTAGCTGGAGCTGCAGGCGCATA A C CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1175427733 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_247273,RMVar_hsa_circ_339616,RMVar_hsa_circ_366137,RMVar_hsa_circ_247270,RMVar_hsa_circ_348745,RMVar_hsa_circ_295461,RMVar_hsa_circ_247272 18757 RMVar_ID_18757 Human_SNP_ID_333148582 A-to-I Human chr7 + 102174684 102174684 102174684 AAAGGAAGGATGGGCCAGGCGCAGTGGCTCACACCCATAATCCCAGCACTTTGGGAGGCCAAGGC AAAGGAAGGATGGGCCAGGCGCAGTGGCTCACGCCCATAATCCCAGCACTTTGGGAGGCCAAGGC A G CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1373728651 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_247273,RMVar_hsa_circ_339616,RMVar_hsa_circ_366137,RMVar_hsa_circ_247270,RMVar_hsa_circ_348745,RMVar_hsa_circ_295461,RMVar_hsa_circ_247272 18758 RMVar_ID_18758 Human_SNP_ID_333149309 A-to-I Human chr7 + 102177243 102177243 102177243 CGAGACCAGCCTGGCCAACATAGTGAAACCCCATCTCTACTAAAAATACAAAAATGAGCCAAGTG CGAGACCAGCCTGGCCAACATAGTGAAACCCCGTCTCTACTAAAAATACAAAAATGAGCCAAGTG A G CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1195838593 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_247273,RMVar_hsa_circ_339616,RMVar_hsa_circ_366137,RMVar_hsa_circ_247270,RMVar_hsa_circ_348745,RMVar_hsa_circ_295461,RMVar_hsa_circ_247272 18759 RMVar_ID_18759 Human_SNP_ID_333186283 A-to-I Human chr7 + 102311438 102311438 102311438 CAACAAGCCCAGCTAATTTTTATATTTTTAGCAGAGACGGGGTTTCCCCATGGTGGTCAGGCTCG CAACAAGCCCAGCTAATTTTTATATTTTTAGCGGAGACGGGGTTTCCCCATGGTGGTCAGGCTCG A G SH2B2 Ensembl:ENSG00000160999 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1563563256 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14547,RMVar_hsa_circ_280947,RMVar_hsa_circ_341845,RMVar_hsa_circ_26634 18760 RMVar_ID_18760 Human_SNP_ID_333187808 A-to-I Human chr7 + 102316747 102316747 102316747 ATCTCTAAAAAATAAAAAATAAGGCTGGGCGCAATGGCTTACACCTATAATCGCAGCACTTTGGG ATCTCTAAAAAATAAAAAATAAGGCTGGGCGCGATGGCTTACACCTATAATCGCAGCACTTTGGG A G SH2B2 Ensembl:ENSG00000160999 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs557934219 Functional Loss SNV dbSNP153 33..33 33 - - - 18761 RMVar_ID_18761 Human_SNP_ID_333203117 A-to-I Human chr7 + 102378419 102378419 102378419 TTGGGCTCCTGGCCTTGTGAGCTGCCTGCCTCAGCTTCCCAAAGTGCTGGGATTACAGGCGTGAG TTGGGCTCCTGGCCTTGTGAGCTGCCTGCCTCTGCTTCCCAAAGTGCTGGGATTACAGGCGTGAG A T PRKRIP1,AC091390.5 Ensembl:ENSG00000128563,Ensembl:ENSG00000239969 Protein coding,Pseudogene intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1416078087 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122154,RMVar_hsa_circ_99697,RMVar_hsa_circ_247294,RMVar_hsa_circ_247295,RMVar_hsa_circ_247298,RMVar_hsa_circ_81383,RMVar_hsa_circ_110127,RMVar_hsa_circ_247304,RMVar_hsa_circ_120030,RMVar_hsa_circ_247301,RMVar_hsa_circ_112007,RMVar_hsa_circ_247303 18762 RMVar_ID_18762 Human_SNP_ID_333203409 A-to-I Human chr7 + 102379290 102379290 102379290 AAACTCCTGGCCTCAAGTGATCTGCCTGCCTCAGCCTCCCCAAGTGCTGGGATCAAAGGTGTGAG AAACTCCTGGCCTCAAGTGATCTGCCTGCCTCGGCCTCCCCAAGTGCTGGGATCAAAGGTGTGAG A G PRKRIP1,AC091390.5 Ensembl:ENSG00000128563,Ensembl:ENSG00000239969 Protein coding,Pseudogene intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1554566885 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5251281 RMVar_hsa_circ_122154,RMVar_hsa_circ_99697,RMVar_hsa_circ_247294,RMVar_hsa_circ_247295,RMVar_hsa_circ_247298,RMVar_hsa_circ_81383,RMVar_hsa_circ_110127,RMVar_hsa_circ_247304,RMVar_hsa_circ_120030,RMVar_hsa_circ_247301,RMVar_hsa_circ_112007,RMVar_hsa_circ_247303 18763 RMVar_ID_18763 Human_SNP_ID_333203603 A-to-I Human chr7 + 102380151 102380151 102380151 AAAATTAGCTGGGCGTGGTGGTGCTTGTCTGTAATCCCAGCTACTTGGGAGGCTGAGGCATGAGA AAAATTAGCTGGGCGTGGTGGTGCTTGTCTGTCATCCCAGCTACTTGGGAGGCTGAGGCATGAGA A C PRKRIP1,AC091390.5 Ensembl:ENSG00000128563,Ensembl:ENSG00000239969 Protein coding,Pseudogene intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1403863463 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17429568,Human_RBP_ID_18520538 RMVar_hsa_circ_122154,RMVar_hsa_circ_99697,RMVar_hsa_circ_247294,RMVar_hsa_circ_247295,RMVar_hsa_circ_247298,RMVar_hsa_circ_81383,RMVar_hsa_circ_110127,RMVar_hsa_circ_247304,RMVar_hsa_circ_120030,RMVar_hsa_circ_247301,RMVar_hsa_circ_112007,RMVar_hsa_circ_247303 18764 RMVar_ID_18764 Human_SNP_ID_333204700 A-to-I Human chr7 + 102384164 102384164 102384164 GAGGTCAGGAGTTTGAGAGGACAACATGATGAAACTCCATCTCTACTGAAACACAAAAATTAGCT GAGGTCAGGAGTTTGAGAGGACAACATGATGAGACTCCATCTCTACTGAAACACAAAAATTAGCT A G PRKRIP1 Ensembl:ENSG00000128563 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1216115084 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122154,RMVar_hsa_circ_99697,RMVar_hsa_circ_247294,RMVar_hsa_circ_247295,RMVar_hsa_circ_247298,RMVar_hsa_circ_81383,RMVar_hsa_circ_110127,RMVar_hsa_circ_247304,RMVar_hsa_circ_120030,RMVar_hsa_circ_247301,RMVar_hsa_circ_112007,RMVar_hsa_circ_247303 18765 RMVar_ID_18765 Human_SNP_ID_333205263 A-to-I Human chr7 + 102386619 102386619 102386619 GTTTGTTTGTATTTGAGACTGAGTCTCGCTCTATCGCCCAGGCTGGAGTGCAGTGGTGCGATCTC GTTTGTTTGTATTTGAGACTGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCAGTGGTGCGATCTC A G PRKRIP1 Ensembl:ENSG00000128563 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1250478248 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15953550 RMVar_hsa_circ_122154,RMVar_hsa_circ_99697,RMVar_hsa_circ_247294,RMVar_hsa_circ_247295,RMVar_hsa_circ_247298,RMVar_hsa_circ_81383,RMVar_hsa_circ_110127,RMVar_hsa_circ_247304,RMVar_hsa_circ_120030,RMVar_hsa_circ_247301,RMVar_hsa_circ_112007,RMVar_hsa_circ_247303 18766 RMVar_ID_18766 Human_SNP_ID_333206037 A-to-I Human chr7 + 102389709 102389709 102389709 CTCACTGCAACCTCCGCCTCCTGGGTTCAAGCAATCCTCCTGCCTCAGCCTTCCAAGTACCTGAG CTCACTGCAACCTCCGCCTCCTGGGTTCAAGCCATCCTCCTGCCTCAGCCTTCCAAGTACCTGAG A C PRKRIP1 Ensembl:ENSG00000128563 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1554569399 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122154,RMVar_hsa_circ_99697,RMVar_hsa_circ_247294,RMVar_hsa_circ_247295,RMVar_hsa_circ_247298,RMVar_hsa_circ_81383,RMVar_hsa_circ_110127,RMVar_hsa_circ_247304,RMVar_hsa_circ_120030,RMVar_hsa_circ_247301,RMVar_hsa_circ_112007,RMVar_hsa_circ_247303 18767 RMVar_ID_18767 Human_SNP_ID_333207320 A-to-I Human chr7 + 102394570 102394570 102394570 TGGGGTTTCACCATGTTGGCCATGCTGGTCTCAAACTCCTGACTTCAAGTGATCTGCCCATCTCG TGGGGTTTCACCATGTTGGCCATGCTGGTCTCCAACTCCTGACTTCAAGTGATCTGCCCATCTCG A C PRKRIP1 Ensembl:ENSG00000128563 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1452723694 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122154,RMVar_hsa_circ_99697,RMVar_hsa_circ_247294,RMVar_hsa_circ_247295,RMVar_hsa_circ_247298,RMVar_hsa_circ_81383,RMVar_hsa_circ_110127,RMVar_hsa_circ_247304,RMVar_hsa_circ_120030,RMVar_hsa_circ_247301,RMVar_hsa_circ_112007,RMVar_hsa_circ_247303 18768 RMVar_ID_18768 Human_SNP_ID_333207512 A-to-I Human chr7 + 102395441 102395441 102395441 AAAATTAACTGGGTGTGGTGGCATGCGCCTGTAGTCTCAGCTACTCAGGAGGCTGAGGTGGGAGG AAAATTAACTGGGTGTGGTGGCATGCGCCTGTGGTCTCAGCTACTCAGGAGGCTGAGGTGGGAGG A G PRKRIP1 Ensembl:ENSG00000128563 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1220213756 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26053361 RMVar_hsa_circ_122154,RMVar_hsa_circ_99697,RMVar_hsa_circ_247294,RMVar_hsa_circ_247295,RMVar_hsa_circ_247298,RMVar_hsa_circ_81383,RMVar_hsa_circ_110127,RMVar_hsa_circ_247304,RMVar_hsa_circ_120030,RMVar_hsa_circ_247301,RMVar_hsa_circ_112007,RMVar_hsa_circ_247303 18769 RMVar_ID_18769 Human_SNP_ID_333208228 A-to-I Human chr7 + 102397431 102397431 102397431 GCCTGGTGTGGTGGTGTACGCCTGAGAGTCCTAACTATTCTGGAGACTGAACCGGGAGGATCACT GCCTGGTGTGGTGGTGTACGCCTGAGAGTCCTGACTATTCTGGAGACTGAACCGGGAGGATCACT A G PRKRIP1 Ensembl:ENSG00000128563 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1193699117 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3033286,Human_RBP_ID_3862576,Human_RBP_ID_5404459,Human_RBP_ID_8914541 RMVar_hsa_circ_247304,RMVar_hsa_circ_120030,RMVar_hsa_circ_303660,RMVar_hsa_circ_350579,RMVar_hsa_circ_39231,RMVar_hsa_circ_247306 18770 RMVar_ID_18770 Human_SNP_ID_333209201 A-to-I Human chr7 + 102400655 102400655 102400655 CTGTGTAGATACTAACTTTATTTATTATTTTGAGATGGAGTTTTGCTCTTGTTGCCCAGGCTGAG CTGTGTAGATACTAACTTTATTTATTATTTTGTGATGGAGTTTTGCTCTTGTTGCCCAGGCTGAG A T PRKRIP1 Ensembl:ENSG00000128563 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs573913145 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_247304,RMVar_hsa_circ_120030,RMVar_hsa_circ_350579,RMVar_hsa_circ_39231,RMVar_hsa_circ_247306,RMVar_hsa_circ_247309,RMVar_hsa_circ_281706,RMVar_hsa_circ_292074,RMVar_hsa_circ_247308,RMVar_hsa_circ_247312,RMVar_hsa_circ_283289,RMVar_hsa_circ_285897,RMVar_hsa_circ_247313,RMVar_hsa_circ_247311 18771 RMVar_ID_18771 Human_SNP_ID_333209335 A-to-I Human chr7 + 102401232 102401232 102401232 ACAGTGCATACCAATAGAGGTATGGATAGATCAATAGGTGTGTGATAAAGAAAATCCAGCACAAC ACAGTGCATACCAATAGAGGTATGGATAGATCGATAGGTGTGTGATAAAGAAAATCCAGCACAAC A G PRKRIP1 Ensembl:ENSG00000128563 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7385225 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_1628,GWAS_ID_1629 RMVar_hsa_circ_247304,RMVar_hsa_circ_120030,RMVar_hsa_circ_350579,RMVar_hsa_circ_39231,RMVar_hsa_circ_247306,RMVar_hsa_circ_247309,RMVar_hsa_circ_281706,RMVar_hsa_circ_292074,RMVar_hsa_circ_247308,RMVar_hsa_circ_247312,RMVar_hsa_circ_283289,RMVar_hsa_circ_285897,RMVar_hsa_circ_247313,RMVar_hsa_circ_247311 18772 RMVar_ID_18772 Human_SNP_ID_333209819 A-to-I Human chr7 + 102403040 102403040 102403040 GGGATTACAGGTGCCTGCCACCTGGCCTGGCTAATTTTTGTGTTTTTAGTAGAGACAGGGTTTCA GGGATTACAGGTGCCTGCCACCTGGCCTGGCTGATTTTTGTGTTTTTAGTAGAGACAGGGTTTCA A G PRKRIP1 Ensembl:ENSG00000128563 Protein coding intron GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-Seq:(High) rs1277964042 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_247304,RMVar_hsa_circ_120030,RMVar_hsa_circ_350579,RMVar_hsa_circ_39231,RMVar_hsa_circ_247306,RMVar_hsa_circ_247309,RMVar_hsa_circ_281706,RMVar_hsa_circ_292074,RMVar_hsa_circ_247308,RMVar_hsa_circ_247312,RMVar_hsa_circ_283289,RMVar_hsa_circ_285897,RMVar_hsa_circ_247313,RMVar_hsa_circ_247311 18773 RMVar_ID_18773 Human_SNP_ID_333209834 A-to-I Human chr7 + 102403127 102403127 102403127 GAACTCTGGACCTCAGGTGATCTGCCCACCTCAGCTTCCCAGTGTGCTGGGATTACAGGAGTGAG GAACTCTGGACCTCAGGTGATCTGCCCACCTCTGCTTCCCAGTGTGCTGGGATTACAGGAGTGAG A T PRKRIP1 Ensembl:ENSG00000128563 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1380076729 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_247304,RMVar_hsa_circ_120030,RMVar_hsa_circ_350579,RMVar_hsa_circ_39231,RMVar_hsa_circ_247306,RMVar_hsa_circ_247309,RMVar_hsa_circ_281706,RMVar_hsa_circ_292074,RMVar_hsa_circ_247308,RMVar_hsa_circ_247312,RMVar_hsa_circ_283289,RMVar_hsa_circ_285897,RMVar_hsa_circ_247313,RMVar_hsa_circ_247311 18774 RMVar_ID_18774 Human_SNP_ID_333210040 A-to-I Human chr7 + 102403899 102403899 102403899 GCTTTAGAATCAGTCATTTGGTGGCTGGGCACAGTGGCCTGTAATCTCAGCACTTTGGGAGGCTG GCTTTAGAATCAGTCATTTGGTGGCTGGGCACGGTGGCCTGTAATCTCAGCACTTTGGGAGGCTG A G PRKRIP1 Ensembl:ENSG00000128563 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs114902206 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_247304,RMVar_hsa_circ_120030,RMVar_hsa_circ_350579,RMVar_hsa_circ_39231,RMVar_hsa_circ_247306,RMVar_hsa_circ_247309,RMVar_hsa_circ_281706,RMVar_hsa_circ_292074,RMVar_hsa_circ_247308,RMVar_hsa_circ_247312,RMVar_hsa_circ_283289,RMVar_hsa_circ_285897,RMVar_hsa_circ_247313,RMVar_hsa_circ_247311 18775 RMVar_ID_18775 Human_SNP_ID_333210055 A-to-I Human chr7 + 102403983 102403983 102403983 GGCCAGGAATTTAAAACCAGCCTGGACAACATAGCCAGACCTGTCTCTACAAAATAAACATAAAA GGCCAGGAATTTAAAACCAGCCTGGACAACATGGCCAGACCTGTCTCTACAAAATAAACATAAAA A G PRKRIP1 Ensembl:ENSG00000128563 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs944034669 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_247304,RMVar_hsa_circ_120030,RMVar_hsa_circ_350579,RMVar_hsa_circ_39231,RMVar_hsa_circ_247306,RMVar_hsa_circ_247309,RMVar_hsa_circ_281706,RMVar_hsa_circ_292074,RMVar_hsa_circ_247308,RMVar_hsa_circ_247312,RMVar_hsa_circ_283289,RMVar_hsa_circ_285897,RMVar_hsa_circ_247313,RMVar_hsa_circ_247311 18776 RMVar_ID_18776 Human_SNP_ID_333212103 A-to-I Human chr7 + 102412066 102412066 102412066 CACCATGCCCGGCTGATTTTTGTGTTTTTAGTAGAGATGGTGTTTCACCATGTTGGCCAGACTAG CACCATGCCCGGCTGATTTTTGTGTTTTTAGTGGAGATGGTGTTTCACCATGTTGGCCAGACTAG A G PRKRIP1 Ensembl:ENSG00000128563 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs974029192 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15954097 RMVar_hsa_circ_247304,RMVar_hsa_circ_120030 18777 RMVar_ID_18777 Human_SNP_ID_333212109 A-to-I Human chr7 + 102412083 102412083 102412083 TTTTGTGTTTTTAGTAGAGATGGTGTTTCACCATGTTGGCCAGACTAGTCTCGAACTCCACCCAC TTTTGTGTTTTTAGTAGAGATGGTGTTTCACCGTGTTGGCCAGACTAGTCTCGAACTCCACCCAC A G PRKRIP1 Ensembl:ENSG00000128563 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1326980427 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_247304,RMVar_hsa_circ_120030 18778 RMVar_ID_18778 Human_SNP_ID_333212113 A-to-I Human chr7 + 102412097 102412097 102412097 TAGAGATGGTGTTTCACCATGTTGGCCAGACTAGTCTCGAACTCCACCCACCTCGGCCTCCCAAA TAGAGATGGTGTTTCACCATGTTGGCCAGACTGGTCTCGAACTCCACCCACCTCGGCCTCCCAAA A G PRKRIP1 Ensembl:ENSG00000128563 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1162111031 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7668160,Human_RBP_ID_15954098 RMVar_hsa_circ_247304,RMVar_hsa_circ_120030 18779 RMVar_ID_18779 Human_SNP_ID_333212813 A-to-I Human chr7 + 102415273 102415273 102415273 AAGCTCTGTTTTTTGAAATGGAGTCTTGCTCCATCACTCATGTTGGAGTGCAGTGGCGCCAGCTC AAGCTCTGTTTTTTGAAATGGAGTCTTGCTCCGTCACTCATGTTGGAGTGCAGTGGCGCCAGCTC A G PRKRIP1 Ensembl:ENSG00000128563 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1049603614 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_247304,RMVar_hsa_circ_120030 18780 RMVar_ID_18780 Human_SNP_ID_333212854 A-to-I Human chr7 + 102415497 102415497 102415497 ATTTCAGGTGATTCACCCGCGTTGGCCTCCCAAAGCGCTGGGATTACAGGCGTGAGCCACCGCAC ATTTCAGGTGATTCACCCGCGTTGGCCTCCCAGAGCGCTGGGATTACAGGCGTGAGCCACCGCAC A G PRKRIP1 Ensembl:ENSG00000128563 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1267231064 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_247304,RMVar_hsa_circ_120030 18781 RMVar_ID_18781 Human_SNP_ID_333214557 A-to-I Human chr7 + 102421642 102421641 102421642 AACACGGTGAAACCCCGTCTCTACTAAAATATAAAAAATTAGCCGGGTGTAGTGTCACACACCTG AACACGGTGAAACCCCGTCTCTACTAAAATAT_AAAAATTAGCCGGGTGTAGTGTCACACACCTG TA T PRKRIP1 Ensembl:ENSG00000128563 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1405048050 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_247304,RMVar_hsa_circ_120030 18782 RMVar_ID_18782 Human_SNP_ID_333216394 A-to-I Human chr7 + 102428011 102428007 102428011 CAGGCTGGGGTGCAGTGGCGTGATCTCGGCTCACTGCAACCTCCACCTCTCGGGCTCAAGCCATT CAGGCTGGGGTGCAGTGGCGTGATCTCGG____CTGCAACCTCCACCTCTCGGGCTCAAGCCATT GCTCA G RF00017-4685,RF00017-4498 RNACentral:URS0000985E23,RNACentral:URS0000923951 SRP RNA,SRP RNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs767490021 Functional Loss DEL dbSNP153 30..33 33 - - - 18783 RMVar_ID_18783 Human_SNP_ID_333218415 A-to-I Human chr7 + 102435128 102435127 102435128 CCTGTCTCTACCAAAAATACCAAAAATTAGCCAGGTATGGTGGCACACACATGTAGTCCCAGCTA CCTGTCTCTACCAAAAATACCAAAAATTAGCC_GGTATGGTGGCACACACATGTAGTCCCAGCTA CA C ORAI2 Ensembl:ENSG00000160991 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs774229057 Functional Loss DEL dbSNP153 33..33 33 - - - 18784 RMVar_ID_18784 Human_SNP_ID_333218440 A-to-I Human chr7 + 102435205 102435205 102435205 AGGCGGGAGGATCGCTTGAGCCTGGGAGGTAGAATTTGCAGGGAGCTGAGATTGTGCCACTGCAC AGGCGGGAGGATCGCTTGAGCCTGGGAGGTAGGATTTGCAGGGAGCTGAGATTGTGCCACTGCAC A G ORAI2 Ensembl:ENSG00000160991 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1317667714 Functional Loss SNV dbSNP153 33..33 33 - - - 18785 RMVar_ID_18785 Human_SNP_ID_333218613 A-to-I Human chr7 + 102435796 102435794 102435796 AGCTGGGATTACAGGCGCCCACCACCATGCCCAGTTACTTTTTGTATTTTTAGAAGAGACAGGTT AGCTGGGATTACAGGCGCCCACCACCATGCC__GTTACTTTTTGTATTTTTAGAAGAGACAGGTT CCA C ORAI2 Ensembl:ENSG00000160991 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs775030127 Functional Loss DEL dbSNP153 32..33 33 - - - 18786 RMVar_ID_18786 Human_SNP_ID_333219861 A-to-I Human chr7 + 102440962 102440962 102440962 TCACCCAGGCTGGAGTGCAGTGGTGTGATTTCAGCTCACTGCAGCCTCTGCCTCCTGGATTCAAG TCACCCAGGCTGGAGTGCAGTGGTGTGATTTCCGCTCACTGCAGCCTCTGCCTCCTGGATTCAAG A C ORAI2 Ensembl:ENSG00000160991 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1054726296 Functional Loss SNV dbSNP153 33..33 33 - - - 18787 RMVar_ID_18787 Human_SNP_ID_333220355 A-to-I Human chr7 + 102442735 102442735 102442735 AAAATTAGCCAGGCGTGGTGGCTGGCACCTGTAACCCCAGCTTCTCGGGAGGCTGAAGTGGGAGG AAAATTAGCCAGGCGTGGTGGCTGGCACCTGTTACCCCAGCTTCTCGGGAGGCTGAAGTGGGAGG A T ORAI2 Ensembl:ENSG00000160991 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1031097030 Functional Loss SNV dbSNP153 33..33 33 - - - 18788 RMVar_ID_18788 Human_SNP_ID_333220733 A-to-I Human chr7 + 102443762 102443762 102443762 GTAGTCTCGCTCTGTCTCCCAGGCTGGAGCACAATGGCACGATCTTGGCTCACTGCAACCTTTGC GTAGTCTCGCTCTGTCTCCCAGGCTGGAGCACGATGGCACGATCTTGGCTCACTGCAACCTTTGC A G ORAI2 Ensembl:ENSG00000160991 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1276602718 Functional Loss SNV dbSNP153 33..33 33 - - - 18789 RMVar_ID_18789 Human_SNP_ID_333222332 A-to-I Human chr7 + 102448590 102448590 102448590 AAAATTAGCTGGGCGTGGTGGCGGGCGCCTGTAGCCCCAGCTACTTGGGAGGCTGAGGCGGGAGA AAAATTAGCTGGGCGTGGTGGCGGGCGCCTGTTGCCCCAGCTACTTGGGAGGCTGAGGCGGGAGA A T ORAI2 Ensembl:ENSG00000160991 Protein coding 3'UTR GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;Bronchiolar epithelium,BEP2D cell line - 29129909,30559470,31158229 RNA-Seq:(High) rs1269651277 Functional Loss SNV dbSNP153 33..33 33 - - - 18790 RMVar_ID_18790 Human_SNP_ID_333222660 A-to-I Human chr7 + 102449758 102449758 102449758 TAAATTAGCTGGGCGTGGTGGTGCATGCCTGTAGTTCCAGCTACTTGGGAGGCTGAGGTGGGAGG TAAATTAGCTGGGCGTGGTGGTGCATGCCTGTGGTTCCAGCTACTTGGGAGGCTGAGGTGGGAGG A G ORAI2 Ensembl:ENSG00000160991 Protein coding 3'UTR GSE38233;GSE107867 cultured B-cells;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 24183664,30559470 RNA-Seq:(High) rs905008637 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26550761 18791 RMVar_ID_18791 Human_SNP_ID_333223319 A-to-I Human chr7 + 102452285 102452285 102452285 CCAAGTAGCTGGGATTACAGGCACGCACCACCATGCTTGGCTAATTTTTGTATTTTTAGTAGAGA CCAAGTAGCTGGGATTACAGGCACGCACCACCGTGCTTGGCTAATTTTTGTATTTTTAGTAGAGA A G ORAI2 Ensembl:ENSG00000160991 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs977715225 Functional Loss SNV dbSNP153 33..33 33 - - - 18792 RMVar_ID_18792 Human_SNP_ID_333223376 A-to-I Human chr7 + 102452550 102452550 102452550 GGCTCCAGCTTCTGGGCGCAAGCAATCCTCCCACCTCAGTCTCCCAAGTAGCTACACTTGGGAGA GGCTCCAGCTTCTGGGCGCAAGCAATCCTCCCGCCTCAGTCTCCCAAGTAGCTACACTTGGGAGA A G ORAI2 Ensembl:ENSG00000160991 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1413195070 Functional Loss SNV dbSNP153 33..33 33 - - - 18793 RMVar_ID_18793 Human_SNP_ID_333223501 A-to-I Human chr7 + 102452996 102452996 102452996 TAATTTTTGTTGTTGTCGTTGGTTTTTGAGATAGAGTTTCGCTCTTGTTGCCCAGGCTGGAGTGC TAATTTTTGTTGTTGTCGTTGGTTTTTGAGATGGAGTTTCGCTCTTGTTGCCCAGGCTGGAGTGC A G ORAI2 Ensembl:ENSG00000160991 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893296364 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3824277,Human_RBP_ID_8653202 18794 RMVar_ID_18794 Human_SNP_ID_333223693 A-to-I Human chr7 + 102453862 102453862 102453862 GTGATTCTCCTGCCTCAGCCTCCTGAGTAGCTAGGATTACAGGCGCCCACCATCACGCCTGGCTA GTGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCGCCCACCATCACGCCTGGCTA A G ORAI2 Ensembl:ENSG00000160991 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1167052420 Functional Loss SNV dbSNP153 33..33 33 - - - 18795 RMVar_ID_18795 Human_SNP_ID_333223717 A-to-I Human chr7 + 102453981 102453981 102453981 GAACTCCTGACCTCAAGTGATCCTCCTGCCTCAGCCTCCCAAAGTGCTGGGATTATAGGCGTGAG GAACTCCTGACCTCAAGTGATCCTCCTGCCTCGGCCTCCCAAAGTGCTGGGATTATAGGCGTGAG A G ORAI2 Ensembl:ENSG00000160991 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs554664663 Functional Loss SNV dbSNP153 33..33 33 - - - 18796 RMVar_ID_18796 Human_SNP_ID_333223783 A-to-I Human chr7 + 102454232 102454231 102454232 GCCTGGGCAACATTACGAGACCCTGTCTCTACAAAAATACAAAAATTACCCGGGCTTGGTGGCTC GCCTGGGCAACATTACGAGACCCTGTCTCTAC_AAAATACAAAAATTACCCGGGCTTGGTGGCTC CA C ORAI2 Ensembl:ENSG00000160991 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1386990000 Functional Loss DEL dbSNP153 33..33 33 - - - 18797 RMVar_ID_18797 Human_SNP_ID_333223799 A-to-I Human chr7 + 102454271 102454271 102454271 CAAAAATTACCCGGGCTTGGTGGCTCGTGCCTATAGTCCCAGCTACTGGGGAGGCTGAGGTGGGA CAAAAATTACCCGGGCTTGGTGGCTCGTGCCTCTAGTCCCAGCTACTGGGGAGGCTGAGGTGGGA A C ORAI2 Ensembl:ENSG00000160991 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs532347620 Functional Loss SNV dbSNP153 33..33 33 - - - 18798 RMVar_ID_18798 Human_SNP_ID_333223816 A-to-I Human chr7 + 102454344 102454344 102454344 TGAGCCCAGGGAGGTTGAGACTGCAGTGAGCCAAGATTGTGCCACTGCACTCCAGCCTGGGTAAA TGAGCCCAGGGAGGTTGAGACTGCAGTGAGCCGAGATTGTGCCACTGCACTCCAGCCTGGGTAAA A G ORAI2 Ensembl:ENSG00000160991 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1036084013 Functional Loss SNV dbSNP153 33..33 33 - - - 18799 RMVar_ID_18799 Human_SNP_ID_333224002 A-to-I Human chr7 + 102455052 102455052 102455052 TCAAAACAAAACAATTAGCTGGGTATGGTGGCACACGCCTGTAGTTCCAGCTACTGGGGAGGCTG TCAAAACAAAACAATTAGCTGGGTATGGTGGCCCACGCCTGTAGTTCCAGCTACTGGGGAGGCTG A C ORAI2 Ensembl:ENSG00000160991 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs972799276 Functional Loss SNV dbSNP153 33..33 33 - - - 18800 RMVar_ID_18800 Human_SNP_ID_333224014 A-to-I Human chr7 + 102455097 102455097 102455097 TCCAGCTACTGGGGAGGCTGAGGGGGAGGATCACTTGAGCCCAGGAGTTCAAGGCTGCAGTGAGC TCCAGCTACTGGGGAGGCTGAGGGGGAGGATCGCTTGAGCCCAGGAGTTCAAGGCTGCAGTGAGC A G ORAI2 Ensembl:ENSG00000160991 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs981858750 Functional Loss SNV dbSNP153 33..33 33 - - - 18801 RMVar_ID_18801 Human_SNP_ID_333224507 A-to-I Human chr7 - 102456945 102456945 102456945 TCACAGCCGTAATCCCAGCTACTCGGGAGGCTAAGGTGGGAGAATTGCTTGAACCTGGGAGGCGG TCACAGCCGTAATCCCAGCTACTCGGGAGGCTGAGGTGGGAGAATTGCTTGAACCTGGGAGGCGG T C ALKBH4 Ensembl:ENSG00000160993 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs746589402 Functional Loss SNV dbSNP153 33..33 33 - - - 18802 RMVar_ID_18802 Human_SNP_ID_333224531 A-to-I Human chr7 - 102457011 102457011 102457011 CAGCCTGGCCAACACGGTGAAAACCCGTCTCTACAAAAACTACAAAAATTAGCCGGGTGTGGTGA CAGCCTGGCCAACACGGTGAAAACCCGTCTCTGCAAAAACTACAAAAATTAGCCGGGTGTGGTGA T C ALKBH4 Ensembl:ENSG00000160993 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs561630818 Functional Loss SNV dbSNP153 33..33 33 - - - 18803 RMVar_ID_18803 Human_SNP_ID_333226119 A-to-I Human chr7 - 102462188 102462188 102462188 CATATCTGCCCCTCCCCCCTCCAGATCTTTCTAAAATTCACATTTGACCTCGTCACTCCTTTAAA CATATCTGCCCCTCCCCCCTCCAGATCTTTCTGAAATTCACATTTGACCTCGTCACTCCTTTAAA T C ALKBH4 Ensembl:ENSG00000160993 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1322163163 Functional Loss SNV dbSNP153 33..33 33 - - - 18804 RMVar_ID_18804 Human_SNP_ID_333235856 A-to-I Human chr7 - 102493273 102493273 102493273 CTCCCTCCCTGGCCTGGCAGAGCTGGACCTGCAGCGGACGCTGAGTTTGCAGGCGCCACCTGTGA CTCCCTCCCTGGCCTGGCAGAGCTGGACCTGCGGCGGACGCTGAGTTTGCAGGCGCCACCTGTGA T C RASA4B Ensembl:ENSG00000170667 Protein coding exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1203767469 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_903692,Human_Splice_Rec_903704,Human_Splice_Rec_903742,Human_Splice_Rec_903756,Human_Splice_Rec_903802 RMVar_hsa_circ_100408,RMVar_hsa_circ_247338,RMVar_hsa_circ_119474,RMVar_hsa_circ_247340 18805 RMVar_ID_18805 Human_SNP_ID_333242502 A-to-I Human chr7 - 102534840 102534840 102534840 GCACTGAACTCCTGGGCTCAGGCGATCCTCCCACCTTGGCCTCCCAAAGTGCTGGGATTACAGGC GCACTGAACTCCTGGGCTCAGGCGATCCTCCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGC T C lnc-UPK3BL2-1 RNACentral:URS0000D6DC84 lincRNA intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1334961164 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91883,RMVar_hsa_circ_247345 18806 RMVar_ID_18806 Human_SNP_ID_333242798 A-to-I Human chr7 - 102535889 102535889 102535889 GAGGATCACCTGAGGTCAGGAGTTTGAGACCAACCTGGCCAACATGGTGAAAACCCGTCTCTACA GAGGATCACCTGAGGTCAGGAGTTTGAGACCAGCCTGGCCAACATGGTGAAAACCCGTCTCTACA T C lnc-UPK3BL2-1 RNACentral:URS0000D6DC84 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202569806 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8271756 RMVar_hsa_circ_91883,RMVar_hsa_circ_247345 18807 RMVar_ID_18807 Human_SNP_ID_333245249 A-to-I Human chr7 - 102545409 102545409 102545409 GTCTCAAACTTCTGACCTCAGATGATCCGCCCACCTTGGCCACCCAAAGTGCTGGGATTACAGGT GTCTCAAACTTCTGACCTCAGATGATCCGCCCGCCTTGGCCACCCAAAGTGCTGGGATTACAGGT T C POLR2J3,AC093668.1 Ensembl:ENSG00000168255,Ensembl:ENSG00000270249 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1457868591 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_903956 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_103185,RMVar_hsa_circ_247350,RMVar_hsa_circ_247351,RMVar_hsa_circ_247353,RMVar_hsa_circ_102748,RMVar_hsa_circ_247354 18808 RMVar_ID_18808 Human_SNP_ID_333245268 A-to-I Human chr7 - 102545476 102545476 102545476 GTGCCACCACGACTGACTAATTTTGTATCTTTAGTAGAGACGGGGTTTTTCCACATTGGTCAGGC GTGCCACCACGACTGACTAATTTTGTATCTTTGGTAGAGACGGGGTTTTTCCACATTGGTCAGGC T C POLR2J3,AC093668.1 Ensembl:ENSG00000168255,Ensembl:ENSG00000270249 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1436529661 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10370488,Human_RBP_ID_23080878,Human_RBP_ID_23196314,Human_RBP_ID_26132809 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_103185,RMVar_hsa_circ_247350,RMVar_hsa_circ_247351,RMVar_hsa_circ_247353,RMVar_hsa_circ_102748,RMVar_hsa_circ_247354 18809 RMVar_ID_18809 Human_SNP_ID_333245635 A-to-I Human chr7 - 102547670 102547670 102547670 TCCATGTTGGTCAGGCTGGTCTTGAACTCCCAACCTCGGGTGATCCGCCTGCGTTGGCCTCCCAA TCCATGTTGGTCAGGCTGGTCTTGAACTCCCATCCTCGGGTGATCCGCCTGCGTTGGCCTCCCAA T A POLR2J3,AC093668.1 Ensembl:ENSG00000168255,Ensembl:ENSG00000270249 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1185797451 Functional Loss SNV dbSNP153 33..33 33 - - - 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_103185,RMVar_hsa_circ_247350,RMVar_hsa_circ_247351,RMVar_hsa_circ_247353,RMVar_hsa_circ_102748,RMVar_hsa_circ_247354 18810 RMVar_ID_18810 Human_SNP_ID_333245873 A-to-I Human chr7 - 102548192 102548192 102548192 TGCAGCGTATGATAAAAACGGCATTTCAGGCCAGGCGTGGTGGCTCATGCCTGTCACCCCAGCAC TGCAGCGTATGATAAAAACGGCATTTCAGGCCGGGCGTGGTGGCTCATGCCTGTCACCCCAGCAC T C POLR2J3,AC093668.1 Ensembl:ENSG00000168255,Ensembl:ENSG00000270249 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1274619128 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7783778,Human_RBP_ID_21558657,Human_RBP_ID_22483572,Human_RBP_ID_22832977,Human_RBP_ID_27103329 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_103185,RMVar_hsa_circ_247350,RMVar_hsa_circ_247351,RMVar_hsa_circ_247353,RMVar_hsa_circ_102748,RMVar_hsa_circ_247354 18811 RMVar_ID_18811 Human_SNP_ID_333246035 A-to-I Human chr7 - 102548981 102548981 102548981 TTTGTATTTTTAGTAGAGATGGGTCTAACCATATTGCCTAGGCTGGTCTCGAACTCCTGAGCTCA TTTGTATTTTTAGTAGAGATGGGTCTAACCATCTTGCCTAGGCTGGTCTCGAACTCCTGAGCTCA T G POLR2J3,AC093668.1 Ensembl:ENSG00000168255,Ensembl:ENSG00000270249 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1392926481 Functional Loss SNV dbSNP153 33..33 33 - - - 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_103185,RMVar_hsa_circ_247350,RMVar_hsa_circ_247351,RMVar_hsa_circ_247353,RMVar_hsa_circ_102748,RMVar_hsa_circ_247354 18812 RMVar_ID_18812 Human_SNP_ID_333246048 A-to-I Human chr7 - 102549053 102549053 102549053 TTCTCATGCCTCAACCCTCAGCCTCATGAGTAACTGGGACTACAGGCGTGCACCACCATGCGCAG TTCTCATGCCTCAACCCTCAGCCTCATGAGTAGCTGGGACTACAGGCGTGCACCACCATGCGCAG T C POLR2J3,AC093668.1 Ensembl:ENSG00000168255,Ensembl:ENSG00000270249 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1314870753 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9201566 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_103185,RMVar_hsa_circ_247350,RMVar_hsa_circ_247351,RMVar_hsa_circ_247353,RMVar_hsa_circ_102748,RMVar_hsa_circ_247354 18813 RMVar_ID_18813 Human_SNP_ID_333246780 A-to-I Human chr7 - 102554081 102554081 102554081 TCCTTTTTTGTTTTGTTTTGTTTTGACACAGAATCTTGCTTTGTCACCCAGGCTGGAGTGTAGTG TCCTTTTTTGTTTTGTTTTGTTTTGACACAGAGTCTTGCTTTGTCACCCAGGCTGGAGTGTAGTG T C POLR2J3,AC093668.1 Ensembl:ENSG00000168255,Ensembl:ENSG00000270249 Protein coding,Protein coding intron,intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1298134296 Functional Loss SNV dbSNP153 33..33 33 - - - 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_103185,RMVar_hsa_circ_247350,RMVar_hsa_circ_247351,RMVar_hsa_circ_247353,RMVar_hsa_circ_102748,RMVar_hsa_circ_247354 18814 RMVar_ID_18814 Human_SNP_ID_333248715 A-to-I Human chr7 - 102565301 102565301 102565301 ATGGCGAAACCCCGTCTCTAATACAAATACAAAAATTAGCCAAGCATGGTGGTCACTGTACTCCA ATGGCGAAACCCCGTCTCTAATACAAATACAAGAATTAGCCAAGCATGGTGGTCACTGTACTCCA T C POLR2J3,AC093668.1,POLR2J3:2 Ensembl:ENSG00000168255,Ensembl:ENSG00000270249,Ensembl:ENSG00000285437 Protein coding,Protein coding,Protein coding intron,intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1465443487 Functional Loss SNV dbSNP153 33..33 33 - - - 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_103185,RMVar_hsa_circ_247350,RMVar_hsa_circ_247351,RMVar_hsa_circ_247353,RMVar_hsa_circ_102748,RMVar_hsa_circ_247354 18815 RMVar_ID_18815 Human_SNP_ID_333248726 A-to-I Human chr7 - 102565351 102565351 102565351 AAGGCGGGTGGATCACCTGAGGTCAGGAGTTCAAGACCAGCCTGACCAACATGGCGAAACCCCGT AAGGCGGGTGGATCACCTGAGGTCAGGAGTTCGAGACCAGCCTGACCAACATGGCGAAACCCCGT T C POLR2J3,AC093668.1,POLR2J3:2 Ensembl:ENSG00000168255,Ensembl:ENSG00000270249,Ensembl:ENSG00000285437 Protein coding,Protein coding,Protein coding intron,intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1346285580 Functional Loss SNV dbSNP153 33..33 33 - - - 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_103185,RMVar_hsa_circ_247350,RMVar_hsa_circ_247351,RMVar_hsa_circ_247353,RMVar_hsa_circ_102748,RMVar_hsa_circ_247354 18816 RMVar_ID_18816 Human_SNP_ID_333261484 A-to-I Human chr7 - 102637142 102637142 102637142 CGCCCGACTCGGCCTCCCAAAATGCTGGGATTACAGGCGTGAGCCATCAAGTCTGGCGAGAGAGA CGCCCGACTCGGCCTCCCAAAATGCTGGGATTGCAGGCGTGAGCCATCAAGTCTGGCGAGAGAGA 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 GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1063549 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_671945,Human_RBP_ID_23080886,Human_RBP_ID_26053648 Human_miRNA_ID_1400698,Human_miRNA_ID_1400699 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 18817 RMVar_ID_18817 Human_SNP_ID_333261488 A-to-I Human chr7 - 102637154 102637154 102637154 GACCTTGTGATCCGCCCGACTCGGCCTCCCAAAATGCTGGGATTACAGGCGTGAGCCATCAAGTC GACCTTGTGATCCGCCCGACTCGGCCTCCCAAGATGCTGGGATTACAGGCGTGAGCCATCAAGTC 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 GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1140582 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_314645,Human_RBP_ID_671945,Human_RBP_ID_10317640,Human_RBP_ID_16274675,Human_RBP_ID_22316298,Human_RBP_ID_23070219,Human_RBP_ID_26053648,Human_RBP_ID_26551917 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 18818 RMVar_ID_18818 Human_SNP_ID_333261519 A-to-I 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 GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229,31158229 RNA-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 18819 RMVar_ID_18819 Human_SNP_ID_333261521 A-to-I Human chr7 - 102637234 102637234 102637234 CGCCACCATGCCCAGCTCATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGA CGCCACCATGCCCAGCTCATTTTTGTATTTTTGGTAGAGATGGGGTTTCACCATGTTGGCCAGGA 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 GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1140578 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 18820 RMVar_ID_18820 Human_SNP_ID_333261530 A-to-I Human chr7 - 102637275 102637275 102637275 TTCCTGCTTCAGCCTCCTGAGTAGCTGGGACTACAGGCACACGCCACCATGCCCAGCTCATTTTT TTCCTGCTTCAGCCTCCTGAGTAGCTGGGACTGCAGGCACACGCCACCATGCCCAGCTCATTTTT 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 GSE100210;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229 RNA-Seq:(High) rs1319259032 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 18821 RMVar_ID_18821 Human_SNP_ID_333261532 A-to-I Human chr7 - 102637285 102637285 102637285 TCAAGCGATTTTCCTGCTTCAGCCTCCTGAGTAGCTGGGACTACAGGCACACGCCACCATGCCCA TCAAGCGATTTTCCTGCTTCAGCCTCCTGAGTGGCTGGGACTACAGGCACACGCCACCATGCCCA 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 GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1225641651 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 18822 RMVar_ID_18822 Human_SNP_ID_333263816 A-to-I Human chr7 - 102648003 102648003 102648003 CTCTTGCCTCAACCTCCCAAAGTGCTGGGATTACAGCTGTGAGCCACCGCACCCGGCCGCATTCT CTCTTGCCTCAACCTCCCAAAGTGCTGGGATTGCAGCTGTGAGCCACCGCACCCGGCCGCATTCT T C AC105052.4,AC105052.3 Ensembl:ENSG00000279168,Ensembl:ENSG00000267645 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1169322371 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5222001,Human_RBP_ID_8220833,Human_RBP_ID_10317642,Human_RBP_ID_23070223,Human_RBP_ID_26132831 RMVar_hsa_circ_29342,RMVar_hsa_circ_86928,RMVar_hsa_circ_103174,RMVar_hsa_circ_247377,RMVar_hsa_circ_247378,RMVar_hsa_circ_126641,RMVar_hsa_circ_247380,RMVar_hsa_circ_93180,RMVar_hsa_circ_104936,RMVar_hsa_circ_247382,RMVar_hsa_circ_126703,RMVar_hsa_circ_247383,RMVar_hsa_circ_247384 18823 RMVar_ID_18823 Human_SNP_ID_333263838 A-to-I Human chr7 - 102648075 102648075 102648075 TTTGTATTTTTAGTAGAGATGGGTCTAACCATATTGCCTAGGCTGGTCTCGAACTCCTGAGCTCA TTTGTATTTTTAGTAGAGATGGGTCTAACCATCTTGCCTAGGCTGGTCTCGAACTCCTGAGCTCA T G AC105052.4,AC105052.3 Ensembl:ENSG00000279168,Ensembl:ENSG00000267645 lincRNA,Protein coding intron,intron GSE100210;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229 RNA-Seq:(High) rs1194718828 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29342,RMVar_hsa_circ_86928,RMVar_hsa_circ_103174,RMVar_hsa_circ_247377,RMVar_hsa_circ_247378,RMVar_hsa_circ_126641,RMVar_hsa_circ_247380,RMVar_hsa_circ_93180,RMVar_hsa_circ_104936,RMVar_hsa_circ_247382,RMVar_hsa_circ_126703,RMVar_hsa_circ_247383,RMVar_hsa_circ_247384 18824 RMVar_ID_18824 Human_SNP_ID_333263852 A-to-I Human chr7 - 102648147 102648147 102648147 TTCTCATGCTTCAACCCTCAGCCTCATGAGTAACTGGGACTACAGGCGTGCACCACCATGCGCAG TTCTCATGCTTCAACCCTCAGCCTCATGAGTAGCTGGGACTACAGGCGTGCACCACCATGCGCAG T C AC105052.4,AC105052.3 Ensembl:ENSG00000279168,Ensembl:ENSG00000267645 lincRNA,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1297820866 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29342,RMVar_hsa_circ_86928,RMVar_hsa_circ_103174,RMVar_hsa_circ_247377,RMVar_hsa_circ_247378,RMVar_hsa_circ_126641,RMVar_hsa_circ_247380,RMVar_hsa_circ_93180,RMVar_hsa_circ_104936,RMVar_hsa_circ_247382,RMVar_hsa_circ_126703,RMVar_hsa_circ_247383,RMVar_hsa_circ_247384 18825 RMVar_ID_18825 Human_SNP_ID_333263853 A-to-I Human chr7 - 102648148 102648148 102648148 ATTCTCATGCTTCAACCCTCAGCCTCATGAGTAACTGGGACTACAGGCGTGCACCACCATGCGCA ATTCTCATGCTTCAACCCTCAGCCTCATGAGTTACTGGGACTACAGGCGTGCACCACCATGCGCA T A AC105052.4,AC105052.3 Ensembl:ENSG00000279168,Ensembl:ENSG00000267645 lincRNA,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1464205707 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29342,RMVar_hsa_circ_86928,RMVar_hsa_circ_103174,RMVar_hsa_circ_247377,RMVar_hsa_circ_247378,RMVar_hsa_circ_126641,RMVar_hsa_circ_247380,RMVar_hsa_circ_93180,RMVar_hsa_circ_104936,RMVar_hsa_circ_247382,RMVar_hsa_circ_126703,RMVar_hsa_circ_247383,RMVar_hsa_circ_247384 18826 RMVar_ID_18826 Human_SNP_ID_333266075 A-to-I Human chr7 - 102665324 102665324 102665324 AAAAAGTCCGGGCTTGATGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGACGGGTGGA AAAAAGTCCGGGCTTGATGGCTCACACCTGTACTCCCAGCACTTTGGGAGGCCAAGACGGGTGGA T G AC105052.4,AC105052.3 Ensembl:ENSG00000279168,Ensembl:ENSG00000267645 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1397871506 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_671949,Human_RBP_ID_1691342,Human_RBP_ID_2031972,Human_RBP_ID_3824302,Human_RBP_ID_5105298,Human_RBP_ID_5657904,Human_RBP_ID_7668356,Human_RBP_ID_9201569,Human_RBP_ID_15955206,Human_RBP_ID_23070229,Human_RBP_ID_26053675,Human_RBP_ID_27103346 RMVar_hsa_circ_29342,RMVar_hsa_circ_86928,RMVar_hsa_circ_103174,RMVar_hsa_circ_247377,RMVar_hsa_circ_247378,RMVar_hsa_circ_126641,RMVar_hsa_circ_247380,RMVar_hsa_circ_93180,RMVar_hsa_circ_104936,RMVar_hsa_circ_247382,RMVar_hsa_circ_126703,RMVar_hsa_circ_247383,RMVar_hsa_circ_247384 18827 RMVar_ID_18827 Human_SNP_ID_333290985 A-to-I Human chr7 + 102788039 102788039 102788039 CATACTGGAGTGCAGTGGCGTGATCTTGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAACGATT CATACTGGAGTGCAGTGGCGTGATCTTGGCTCCCTGCAACCTCCGCCTCCCGGGTTCAAACGATT A C FAM185A Ensembl:ENSG00000222011 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1000526735 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61179,RMVar_hsa_circ_364080,RMVar_hsa_circ_351861 18828 RMVar_ID_18828 Human_SNP_ID_333347966 A-to-I Human chr7 - 103037570 103037570 103037570 AAACTCCTGGCCTCAAGAGATCTTCCTACCTCAGCCTCCCAAAGTGCTAGGATTATAGGCGTGAC AAACTCCTGGCCTCAAGAGATCTTCCTACCTCGGCCTCCCAAAGTGCTAGGATTATAGGCGTGAC T C FBXL13 Ensembl:ENSG00000161040 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs966447023 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105700,RMVar_hsa_circ_247397,RMVar_hsa_circ_247412,RMVar_hsa_circ_279551,RMVar_hsa_circ_305506,RMVar_hsa_circ_247411 18829 RMVar_ID_18829 Human_SNP_ID_333347967 A-to-I Human chr7 - 103037585 103037585 103037585 GCCCCAGCTGGTCTCAAACTCCTGGCCTCAAGAGATCTTCCTACCTCAGCCTCCCAAAGTGCTAG GCCCCAGCTGGTCTCAAACTCCTGGCCTCAAGTGATCTTCCTACCTCAGCCTCCCAAAGTGCTAG T A FBXL13 Ensembl:ENSG00000161040 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs200440476 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105700,RMVar_hsa_circ_247397,RMVar_hsa_circ_247412,RMVar_hsa_circ_279551,RMVar_hsa_circ_305506,RMVar_hsa_circ_247411 18830 RMVar_ID_18830 Human_SNP_ID_333347968 A-to-I Human chr7 - 103037588 103037586 103037588 GTTGCCCCAGCTGGTCTCAAACTCCTGGCCTCAAGAGATCTTCCTACCTCAGCCTCCCAAAGTGC GTTGCCCCAGCTGGTCTCAAACTCCTGGCCTC__GAGATCTTCCTACCTCAGCCTCCCAAAGTGC CTT C FBXL13 Ensembl:ENSG00000161040 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs530113349 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_105700,RMVar_hsa_circ_247397,RMVar_hsa_circ_247412,RMVar_hsa_circ_279551,RMVar_hsa_circ_305506,RMVar_hsa_circ_247411 18831 RMVar_ID_18831 Human_SNP_ID_333367808 A-to-I Human chr7 - 103118067 103118067 103118067 CTCCTGCCTCAACCTCCCAAGTAGCTGGGACTACAGGCGCCTGCCACCATGCCTGGCTAGTTTTT CTCCTGCCTCAACCTCCCAAGTAGCTGGGACTGCAGGCGCCTGCCACCATGCCTGGCTAGTTTTT T C NAPEPLD Ensembl:ENSG00000161048 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs980626000 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_276379,RMVar_hsa_circ_247416,RMVar_hsa_circ_15275,RMVar_hsa_circ_247417,RMVar_hsa_circ_285336 18832 RMVar_ID_18832 Human_SNP_ID_333367811 A-to-I Human chr7 - 103118080 103118080 103118080 GGTTCAAGTGATTCTCCTGCCTCAACCTCCCAAGTAGCTGGGACTACAGGCGCCTGCCACCATGC GGTTCAAGTGATTCTCCTGCCTCAACCTCCCACGTAGCTGGGACTACAGGCGCCTGCCACCATGC T G NAPEPLD Ensembl:ENSG00000161048 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1357995307 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_276379,RMVar_hsa_circ_247416,RMVar_hsa_circ_15275,RMVar_hsa_circ_247417,RMVar_hsa_circ_285336 18833 RMVar_ID_18833 Human_SNP_ID_333371964 A-to-I Human chr7 - 103136465 103136465 103136465 CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGTTCGGGCTGCCATACACAGATAATTTCT CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTTCAGGTTCGGGCTGCCATACACAGATAATTTCT T A NAPEPLD Ensembl:ENSG00000161048 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1563367886 Functional Loss SNV dbSNP153 33..33 33 - - - 18834 RMVar_ID_18834 Human_SNP_ID_333373272 A-to-I Human chr7 - 103141451 103141451 103141451 AAGCTCCTGGCTGATCAGGCTGAGGCCCGCAGATCTAAGACCAAGGAAGCACACAAGAGCTATGA AAGCTCCTGGCTGATCAGGCTGAGGCCCGCAGGTCTAAGACCAAGGAAGCACACAAGAGCTATGA T C AC007683.1,NAPEPLD Ensembl:ENSG00000224415,Ensembl:ENSG00000161048 Pseudogene,Protein coding exon,intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1403133751 Functional Loss SNV dbSNP153 33..33 33 - - - 18835 RMVar_ID_18835 Human_SNP_ID_333402420 A-to-I Human chr7 - 103271383 103271383 103271383 GTGAGCACGATGACCACGTGAAGGGACAGTGGAGTGATGAGCTTGAATAGTGATCTTGGAGTTAT GTGAGCACGATGACCACGTGAAGGGACAGTGGGGTGATGAGCTTGAATAGTGATCTTGGAGTTAT T C DPY19L2P2 Ensembl:ENSG00000170629 Pseudogene intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1040089353 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1115163,Human_RBP_ID_18873085 RMVar_hsa_circ_267990 18836 RMVar_ID_18836 Human_SNP_ID_333414357 A-to-I Human chr7 - 103319952 103319952 103319952 TCAGTTTGCTGCAATTTCCGCCTCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCT TCAGTTTGCTGCAATTTCCGCCTCCAGGTTCAGGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCT T C DNAJC2 Ensembl:ENSG00000105821 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1032604057 Functional Loss SNV dbSNP153 33..33 33 - - - 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 18837 RMVar_ID_18837 Human_SNP_ID_333414360 A-to-I Human chr7 - 103319959 103319959 103319959 CGTGATCTCAGTTTGCTGCAATTTCCGCCTCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCG CGTGATCTCAGTTTGCTGCAATTTCCGCCTCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCG T C DNAJC2 Ensembl:ENSG00000105821 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1280973043 Functional Loss SNV dbSNP153 33..33 33 - - - 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 18838 RMVar_ID_18838 Human_SNP_ID_333414366 A-to-I Human chr7 - 103319982 103319982 103319982 TTGTCCAGGCTGGAGTGCAGTGGCGTGATCTCAGTTTGCTGCAATTTCCGCCTCCAGGTTCAAGC TTGTCCAGGCTGGAGTGCAGTGGCGTGATCTCTGTTTGCTGCAATTTCCGCCTCCAGGTTCAAGC T A DNAJC2 Ensembl:ENSG00000105821 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559940336 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15956642 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 18839 RMVar_ID_18839 Human_SNP_ID_333418307 A-to-I Human chr7 - 103335606 103335606 103335606 GGGAGGCGGAAGTTGCAGTGAGCGAAGATTGTACCACTGCAGTCCAACCTGAGCAACAGAGTGAG GGGAGGCGGAAGTTGCAGTGAGCGAAGATTGTGCCACTGCAGTCCAACCTGAGCAACAGAGTGAG T C DNAJC2 Ensembl:ENSG00000105821 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1400366635 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44789 18840 RMVar_ID_18840 Human_SNP_ID_333418369 A-to-I Human chr7 - 103335824 103335824 103335824 AAATTGATTTTTAGCCAGGCACAGTGGGTCACACCTGTAATCCCAACACTTTGGAAGACCAAGGC AAATTGATTTTTAGCCAGGCACAGTGGGTCACCCCTGTAATCCCAACACTTTGGAAGACCAAGGC T G DNAJC2 Ensembl:ENSG00000105821 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1475511496 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44789 18841 RMVar_ID_18841 Human_SNP_ID_333418418 A-to-I Human chr7 - 103335998 103335998 103335998 CACGCCCGGCTAATTTTGTATTTTTCATAGAGACGGGATTTCACCATGTTGGTCAGGCTGGTCTC CACGCCCGGCTAATTTTGTATTTTTCATAGAGGCGGGATTTCACCATGTTGGTCAGGCTGGTCTC T C DNAJC2 Ensembl:ENSG00000105821 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs566798812 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44789 18842 RMVar_ID_18842 Human_SNP_ID_333418419 A-to-I Human chr7 - 103336002 103336002 103336002 CCACCACGCCCGGCTAATTTTGTATTTTTCATAGAGACGGGATTTCACCATGTTGGTCAGGCTGG CCACCACGCCCGGCTAATTTTGTATTTTTCATGGAGACGGGATTTCACCATGTTGGTCAGGCTGG T C DNAJC2 Ensembl:ENSG00000105821 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1563472490 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44789 18843 RMVar_ID_18843 Human_SNP_ID_333418421 A-to-I Human chr7 - 103336011 103336011 103336011 AGGCATGTGCCACCACGCCCGGCTAATTTTGTATTTTTCATAGAGACGGGATTTCACCATGTTGG AGGCATGTGCCACCACGCCCGGCTAATTTTGTGTTTTTCATAGAGACGGGATTTCACCATGTTGG T C DNAJC2 Ensembl:ENSG00000105821 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1431292704 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44789 18844 RMVar_ID_18844 Human_SNP_ID_333423855 A-to-I Human chr7 + 103359042 103359042 103359042 GTCTCACTTTGTTACCAAGGCTGGAGTGCAGTAACATGATCTCAGCTCGCTGCAGCCTCTGCTTC GTCTCACTTTGTTACCAAGGCTGGAGTGCAGTCACATGATCTCAGCTCGCTGCAGCCTCTGCTTC A C PSMC2 Ensembl:ENSG00000161057 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1436592354 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98418,RMVar_hsa_circ_331019,RMVar_hsa_circ_372419,RMVar_hsa_circ_247442,RMVar_hsa_circ_247443,RMVar_hsa_circ_247444,RMVar_hsa_circ_331424,RMVar_hsa_circ_247445,RMVar_hsa_circ_88191,RMVar_hsa_circ_247447 18845 RMVar_ID_18845 Human_SNP_ID_333467393 A-to-I Human chr7 - 103528605 103528605 103528605 AGGATCGCTTGAACCTGGGAGGCAGAGATTGCAGTGAGCTGAGATCATGCCATTGCACTGCAGCC AGGATCGCTTGAACCTGGGAGGCAGAGATTGCGGTGAGCTGAGATCATGCCATTGCACTGCAGCC T C RELN Ensembl:ENSG00000189056 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1009992097 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57734,RMVar_hsa_circ_52686,RMVar_hsa_circ_118658,RMVar_hsa_circ_247453,RMVar_hsa_circ_127535,RMVar_hsa_circ_117049,RMVar_hsa_circ_247455,RMVar_hsa_circ_247456,RMVar_hsa_circ_267449,RMVar_hsa_circ_85484,RMVar_hsa_circ_80585,RMVar_hsa_circ_247458,RMVar_hsa_circ_247459,RMVar_hsa_circ_265420,RMVar_hsa_circ_60392,RMVar_hsa_circ_247461 18846 RMVar_ID_18846 Human_SNP_ID_333565742 A-to-I Human chr7 - 103912258 103912258 103912258 CGGGAGGTGGAGGTTTGCAGTGAGCCGAGATCACACCATTGCACTCCAGCCTGGGCAACAGTGCA CGGGAGGTGGAGGTTTGCAGTGAGCCGAGATCGCACCATTGCACTCCAGCCTGGGCAACAGTGCA T C RELN Ensembl:ENSG00000189056 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs906924086 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_352993,RMVar_hsa_circ_348779,RMVar_hsa_circ_247479,RMVar_hsa_circ_314790,RMVar_hsa_circ_247489,RMVar_hsa_circ_324304,RMVar_hsa_circ_314124,RMVar_hsa_circ_247491,RMVar_hsa_circ_290309 18847 RMVar_ID_18847 Human_SNP_ID_333622127 A-to-I Human chr7 - 104144018 104144018 104144018 ACCCCCTGGGTTCAAGCAATTCTCATGCCTCAACCTCCCAAGTAGCTGGGATTACAGGCACGTGC ACCCCCTGGGTTCAAGCAATTCTCATGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCACGTGC T C ORC5 Ensembl:ENSG00000164815 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs914045689 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3152,RMVar_hsa_circ_289461,RMVar_hsa_circ_321400,RMVar_hsa_circ_359822,RMVar_hsa_circ_296911,RMVar_hsa_circ_277623,RMVar_hsa_circ_74430 18848 RMVar_ID_18848 Human_SNP_ID_333827577 A-to-I Human chr7 - 104952779 104952779 104952779 GGGAGGCCGAGGAGGGTGAATCACCTGAGGTCAGGAGTTCAAGACCATCCTGGCCAACATGGTGA GGGAGGCCGAGGAGGGTGAATCACCTGAGGTCGGGAGTTCAAGACCATCCTGGCCAACATGGTGA T C LINC01004 Ensembl:ENSG00000228393 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909183808 Functional Loss SNV dbSNP153 33..33 33 - - - 18849 RMVar_ID_18849 Human_SNP_ID_333837187 A-to-I Human chr7 - 104991753 104991753 104991753 TTTTTTTTTTTTTTGAGAAAAAGTCTTGCTCTATCACCCAGGCTGGAATGCACTGGCAAGATCTC TTTTTTTTTTTTTTGAGAAAAAGTCTTGCTCTGTCACCCAGGCTGGAATGCACTGGCAAGATCTC T C LINC01004 Ensembl:ENSG00000228393 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1016839796 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7669779,Human_RBP_ID_8272791,Human_RBP_ID_24389146 18850 RMVar_ID_18850 Human_SNP_ID_65500918 A-to-I Human chr2 + 30242427 30242427 30242427 CACCATGCCTGGCTGGTTTTTGTATTTTTAGTAGAGACGGGGTTTTGCCTTGTTGGCCAGGCTGG CACCATGCCTGGCTGGTTTTTGTATTTTTAGTCGAGACGGGGTTTTGCCTTGTTGGCCAGGCTGG A C LBH Ensembl:ENSG00000213626 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1246178887 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98261,RMVar_hsa_circ_81206,RMVar_hsa_circ_198198,RMVar_hsa_circ_198199 18851 RMVar_ID_18851 Human_SNP_ID_65563030 A-to-I Human chr2 + 30478556 30478556 30478556 TACTTCTTAGCTGAGTGTAGTGGTGTGTGCCTATAGTCCTAGTACTTAGGAGGCTGAGACGGGAG TACTTCTTAGCTGAGTGTAGTGGTGTGTGCCTGTAGTCCTAGTACTTAGGAGGCTGAGACGGGAG A G LCLAT1 Ensembl:ENSG00000172954 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1241881800 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1654,RMVar_hsa_circ_272188,RMVar_hsa_circ_288746,RMVar_hsa_circ_53135,RMVar_hsa_circ_8581,RMVar_hsa_circ_198201,RMVar_hsa_circ_321271,RMVar_hsa_circ_198202 18852 RMVar_ID_18852 Human_SNP_ID_65563033 A-to-I Human chr2 + 30478571 30478571 30478571 TGTAGTGGTGTGTGCCTATAGTCCTAGTACTTAGGAGGCTGAGACGGGAGGATCACTTGAGCCCA TGTAGTGGTGTGTGCCTATAGTCCTAGTACTTTGGAGGCTGAGACGGGAGGATCACTTGAGCCCA A T LCLAT1 Ensembl:ENSG00000172954 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1047223873 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1654,RMVar_hsa_circ_272188,RMVar_hsa_circ_288746,RMVar_hsa_circ_53135,RMVar_hsa_circ_8581,RMVar_hsa_circ_198201,RMVar_hsa_circ_321271,RMVar_hsa_circ_198202 18853 RMVar_ID_18853 Human_SNP_ID_65563256 A-to-I Human chr2 + 30479283 30479283 30479283 ACAGGGTCTCATTCAGTCATCCAGGCTGGACTACAGTGGTGTGATCATAGCTCTCTGCAGCTTCC ACAGGGTCTCATTCAGTCATCCAGGCTGGACTGCAGTGGTGTGATCATAGCTCTCTGCAGCTTCC A G LCLAT1 Ensembl:ENSG00000172954 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1029214514 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1654,RMVar_hsa_circ_272188,RMVar_hsa_circ_288746,RMVar_hsa_circ_53135,RMVar_hsa_circ_8581,RMVar_hsa_circ_198201,RMVar_hsa_circ_321271,RMVar_hsa_circ_198202 18854 RMVar_ID_18854 Human_SNP_ID_65768907 A-to-I Human chr2 + 31271765 31271765 31271765 CCCATCTCTACTAAAAATACAAAAATTAGCCGAGCATGGTGGTGCGTGCCTGTAGTCCCAGCTCC CCCATCTCTACTAAAAATACAAAAATTAGCCGGGCATGGTGGTGCGTGCCTGTAGTCCCAGCTCC A G - - Other Unknown GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1484793287 Functional Loss SNV dbSNP153 33..33 33 - - - 18855 RMVar_ID_18855 Human_SNP_ID_65920270 A-to-I Human chr2 - 31843464 31843464 31843464 GTTTTCTGTTCCTGTGTTAGTTTGCCGAGAATAATGGTTTCCAGCTTCATCCATGTACATGCAAA GTTTTCTGTTCCTGTGTTAGTTTGCCGAGAATGATGGTTTCCAGCTTCATCCATGTACATGCAAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1353830814 Functional Loss SNV dbSNP153 33..33 33 - - - 18856 RMVar_ID_18856 Human_SNP_ID_65920332 A-to-I Human chr2 - 31843730 31843728 31843731 AGTTTCTGTGTTTTCGCTTTTTTTTTATTATTATGCTTTAAGTTCTAAGATACATGTGCAGAACC AGTTTCTGTGTTTTCGCTTTTTTTTTATTAT___GCTTTAAGTTCTAAGATACATGTGCAGAACC CATA C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs762724039 Functional Loss DEL dbSNP153 32..34 33 - - - 18857 RMVar_ID_18857 Human_SNP_ID_65921355 A-to-I Human chr2 - 31847513 31847513 31847513 GGATTGCTTGAGGTCAAGAGTTCGAGGCTGCAATGAGCTATGATGGCACTGCTGCACTCCAGCCT GGATTGCTTGAGGTCAAGAGTTCGAGGCTGCAGTGAGCTATGATGGCACTGCTGCACTCCAGCCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs906756624 Functional Loss SNV dbSNP153 33..33 33 - - - 18858 RMVar_ID_18858 Human_SNP_ID_65924324 A-to-I Human chr2 - 31858671 31858671 31858671 AAATCATGCCACTGTACTCCAGCCTGGGCAACAGTGTGAGACTCTGTCTCAAAAAAATAATAATA AAATCATGCCACTGTACTCCAGCCTGGGCAACCGTGTGAGACTCTGTCTCAAAAAAATAATAATA T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1301320784 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23182626 18859 RMVar_ID_18859 Human_SNP_ID_65924887 A-to-I Human chr2 - 31861065 31861065 31861065 GTGGCAGCATGCACCTGTACTCTCAGCTACTCAGGAGGTTGAGGTGAGAGGATCGCTTGAGCCCG GTGGCAGCATGCACCTGTACTCTCAGCTACTCGGGAGGTTGAGGTGAGAGGATCGCTTGAGCCCG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs959527509 Functional Loss SNV dbSNP153 33..33 33 - - - 18860 RMVar_ID_18860 Human_SNP_ID_65938780 A-to-I Human chr2 - 31915045 31915045 31915045 TCACTGTAGCCTCTGCCTCCTGGTCTCAAGCAATCTTCCCACCTCAGCCTCCCAAAGCAATGGGA TCACTGTAGCCTCTGCCTCCTGGTCTCAAGCAGTCTTCCCACCTCAGCCTCCCAAAGCAATGGGA T C MEMO1,DPY30 Ensembl:ENSG00000162959,Ensembl:ENSG00000162961 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006842274 Functional Loss SNV dbSNP153 33..33 33 - - - 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 18861 RMVar_ID_18861 Human_SNP_ID_65949384 A-to-I Human chr2 - 31955778 31955778 31955778 CATGGTAAAACCCTGTCTTTACTGAAAATACAAAATTAGTTGGGCCTAGTGGTGCATGCCTATAA CATGGTAAAACCCTGTCTTTACTGAAAATACAGAATTAGTTGGGCCTAGTGGTGCATGCCTATAA T C MEMO1,DPY30 Ensembl:ENSG00000162959,Ensembl:ENSG00000162961 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1202354563 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13857364 RMVar_hsa_circ_56855,RMVar_hsa_circ_198242,RMVar_hsa_circ_367423 18862 RMVar_ID_18862 Human_SNP_ID_65950495 A-to-I Human chr2 - 31960069 31960069 31960069 CCTCAGCCTCCCATGTAGCTGGGACTATAGGCATGCGCCGCCACACCCGGCTGATTTTTGTACTT CCTCAGCCTCCCATGTAGCTGGGACTATAGGCGTGCGCCGCCACACCCGGCTGATTTTTGTACTT T C MEMO1,DPY30 Ensembl:ENSG00000162959,Ensembl:ENSG00000162961 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1488629463 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56855,RMVar_hsa_circ_367423 18863 RMVar_ID_18863 Human_SNP_ID_65961453 A-to-I Human chr2 - 31999428 31999428 31999428 AAACTTGTGGACTGAAGCAATCTTCCTATCTCAGCCTCCCAGAGTGCTGGGATTACAGGTATGAG AAACTTGTGGACTGAAGCAATCTTCCTATCTCGGCCTCCCAGAGTGCTGGGATTACAGGTATGAG T C MEMO1,DPY30 Ensembl:ENSG00000162959,Ensembl:ENSG00000162961 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1230950984 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56855,RMVar_hsa_circ_367423 18864 RMVar_ID_18864 Human_SNP_ID_65961457 A-to-I Human chr2 - 31999441 31999441 31999441 TCAGGCTGGTCTTAAACTTGTGGACTGAAGCAATCTTCCTATCTCAGCCTCCCAGAGTGCTGGGA TCAGGCTGGTCTTAAACTTGTGGACTGAAGCAGTCTTCCTATCTCAGCCTCCCAGAGTGCTGGGA T C MEMO1,DPY30 Ensembl:ENSG00000162959,Ensembl:ENSG00000162961 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749146357 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56855,RMVar_hsa_circ_367423 18865 RMVar_ID_18865 Human_SNP_ID_65962221 A-to-I Human chr2 - 32001904 32001904 32001904 TGACCTTGTGATCCACCCTCCTTGGCCTCCCAAGGCGCTGGGATTGCAGGTGTGAGCCACCACGC TGACCTTGTGATCCACCCTCCTTGGCCTCCCATGGCGCTGGGATTGCAGGTGTGAGCCACCACGC T A MEMO1,DPY30 Ensembl:ENSG00000162959,Ensembl:ENSG00000162961 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973030125 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56855,RMVar_hsa_circ_367423 18866 RMVar_ID_18866 Human_SNP_ID_65962222 A-to-I Human chr2 - 32001904 32001904 32001904 TGACCTTGTGATCCACCCTCCTTGGCCTCCCAAGGCGCTGGGATTGCAGGTGTGAGCCACCACGC TGACCTTGTGATCCACCCTCCTTGGCCTCCCACGGCGCTGGGATTGCAGGTGTGAGCCACCACGC T G MEMO1,DPY30 Ensembl:ENSG00000162959,Ensembl:ENSG00000162961 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973030125 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56855,RMVar_hsa_circ_367423 18867 RMVar_ID_18867 Human_SNP_ID_65962235 A-to-I Human chr2 - 32001922 32001922 32001922 AGGATGGTCTTGATCTCCTGACCTTGTGATCCACCCTCCTTGGCCTCCCAAGGCGCTGGGATTGC AGGATGGTCTTGATCTCCTGACCTTGTGATCCGCCCTCCTTGGCCTCCCAAGGCGCTGGGATTGC T C MEMO1,DPY30 Ensembl:ENSG00000162959,Ensembl:ENSG00000162961 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1315060614 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56855,RMVar_hsa_circ_367423 18868 RMVar_ID_18868 Human_SNP_ID_65962283 A-to-I Human chr2 - 32002100 32002100 32002100 CGCTGTGTTGCCCAGGCTGGAGGGCACTGGCGAGATCTCAGCTCACTGCAAGCTCTGCCTCCTGG CGCTGTGTTGCCCAGGCTGGAGGGCACTGGCGGGATCTCAGCTCACTGCAAGCTCTGCCTCCTGG T C MEMO1,DPY30 Ensembl:ENSG00000162959,Ensembl:ENSG00000162961 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1225649971 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6910946 RMVar_hsa_circ_56855,RMVar_hsa_circ_367423 18869 RMVar_ID_18869 Human_SNP_ID_65965287 A-to-I Human chr2 + 32011872 32011872 32011872 GGCCAGGAGTTCTAGACCAGCCTGGGGAACATAGGAGACCCTGTTTCTATGAATTTTTTATTTTT GGCCAGGAGTTCTAGACCAGCCTGGGGAACATGGGAGACCCTGTTTCTATGAATTTTTTATTTTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1293899287 Functional Loss SNV dbSNP153 33..33 33 - - - 18870 RMVar_ID_18870 Human_SNP_ID_65965337 A-to-I Human chr2 + 32011981 32011981 32011981 GGTAGGCGGAGGCGGGAGGATCACTTGAGCCCAGGAGGTCGAGGCTACAGTGAGCCATGATCACG GGTAGGCGGAGGCGGGAGGATCACTTGAGCCCTGGAGGTCGAGGCTACAGTGAGCCATGATCACG A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1301947199 Functional Loss SNV dbSNP153 33..33 33 - - - 18871 RMVar_ID_18871 Human_SNP_ID_65965568 A-to-I Human chr2 + 32012666 32012666 32012666 CACCATGTTGGCCAGGGTGGTCTTGAACTCCTAACCTCAGGTGATCCACCGGCCTCGGCCTCCCA CACCATGTTGGCCAGGGTGGTCTTGAACTCCTGACCTCAGGTGATCCACCGGCCTCGGCCTCCCA A G - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1214095364 Functional Loss SNV dbSNP153 33..33 33 - - - 18872 RMVar_ID_18872 Human_SNP_ID_65967595 A-to-I Human chr2 - 32020473 32020473 32020473 AGGTCTTGCTCTGTCACCCAGGTTGGAGTGCAATGGCATGGTCATAGCTCACTGCAACCTTGAAG AGGTCTTGCTCTGTCACCCAGGTTGGAGTGCAGTGGCATGGTCATAGCTCACTGCAACCTTGAAG T C DPY30 Ensembl:ENSG00000162961 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879767100 Functional Loss SNV dbSNP153 33..33 33 - - - 18873 RMVar_ID_18873 Human_SNP_ID_65969095 A-to-I Human chr2 - 32026357 32026357 32026357 CATCCAGGCTGGAGTGCAGTGGCAAGATCACCACTCACCGCAGCTTCAGCCTTCTGGGCTTAAGC CATCCAGGCTGGAGTGCAGTGGCAAGATCACCGCTCACCGCAGCTTCAGCCTTCTGGGCTTAAGC T C DPY30 Ensembl:ENSG00000162961 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1433174911 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13858334 RMVar_hsa_circ_90738,RMVar_hsa_circ_303191,RMVar_hsa_circ_109614,RMVar_hsa_circ_107570,RMVar_hsa_circ_198248,RMVar_hsa_circ_198249,RMVar_hsa_circ_198250 18874 RMVar_ID_18874 Human_SNP_ID_65969097 A-to-I Human chr2 - 32026365 32026364 32026365 CGCTCTGTCATCCAGGCTGGAGTGCAGTGGCAAGATCACCACTCACCGCAGCTTCAGCCTTCTGG CGCTCTGTCATCCAGGCTGGAGTGCAGTGGCA_GATCACCACTCACCGCAGCTTCAGCCTTCTGG CT C DPY30 Ensembl:ENSG00000162961 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1386249387 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_13858334 RMVar_hsa_circ_90738,RMVar_hsa_circ_303191,RMVar_hsa_circ_109614,RMVar_hsa_circ_107570,RMVar_hsa_circ_198248,RMVar_hsa_circ_198249,RMVar_hsa_circ_198250 18875 RMVar_ID_18875 Human_SNP_ID_65969636 A-to-I Human chr2 - 32028203 32028203 32028203 CCAAGGTGGGAGGATCGCTTGGGCTTGGGCCCAGGAGTTTGAGGCTGCAGTGAGCTGTGATCGCA CCAAGGTGGGAGGATCGCTTGGGCTTGGGCCCGGGAGTTTGAGGCTGCAGTGAGCTGTGATCGCA T C DPY30 Ensembl:ENSG00000162961 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1385769866 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90738,RMVar_hsa_circ_303191,RMVar_hsa_circ_109614,RMVar_hsa_circ_107570,RMVar_hsa_circ_198248,RMVar_hsa_circ_198249,RMVar_hsa_circ_198250 18876 RMVar_ID_18876 Human_SNP_ID_65970928 A-to-I Human chr2 - 32032830 32032828 32032831 CACCATGCCCAGATAAGTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGTCAGGCTGG CACCATGCCCAGATAAGTTTTGTATTTTTAG___AGACGGGGTTTCACCATGTTGGTCAGGCTGG TCTA T DPY30 Ensembl:ENSG00000162961 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1289794492 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_90738,RMVar_hsa_circ_109614,RMVar_hsa_circ_107570,RMVar_hsa_circ_198248,RMVar_hsa_circ_198249,RMVar_hsa_circ_198250 18877 RMVar_ID_18877 Human_SNP_ID_65970955 A-to-I Human chr2 - 32032909 32032909 32032909 TCACTGCAACCTCTGCCTCCAGGGTTCAAGCAATTCTCCTGCCTTAGCCTCCTGAATAGCTGGGA TCACTGCAACCTCTGCCTCCAGGGTTCAAGCATTTCTCCTGCCTTAGCCTCCTGAATAGCTGGGA T A DPY30 Ensembl:ENSG00000162961 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs879319268 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90738,RMVar_hsa_circ_109614,RMVar_hsa_circ_107570,RMVar_hsa_circ_198248,RMVar_hsa_circ_198249,RMVar_hsa_circ_198250 18878 RMVar_ID_18878 Human_SNP_ID_65970956 A-to-I Human chr2 - 32032909 32032909 32032909 TCACTGCAACCTCTGCCTCCAGGGTTCAAGCAATTCTCCTGCCTTAGCCTCCTGAATAGCTGGGA TCACTGCAACCTCTGCCTCCAGGGTTCAAGCAGTTCTCCTGCCTTAGCCTCCTGAATAGCTGGGA T C DPY30 Ensembl:ENSG00000162961 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs879319268 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90738,RMVar_hsa_circ_109614,RMVar_hsa_circ_107570,RMVar_hsa_circ_198248,RMVar_hsa_circ_198249,RMVar_hsa_circ_198250 18879 RMVar_ID_18879 Human_SNP_ID_65971880 A-to-I Human chr2 - 32036109 32036109 32036109 ATGGTGGTGTGTGCCTATAGTACCAGCTACTCAGGAGACTGAGGTGGGAGGATTGCTTGAGCCTG ATGGTGGTGTGTGCCTATAGTACCAGCTACTCCGGAGACTGAGGTGGGAGGATTGCTTGAGCCTG T G DPY30 Ensembl:ENSG00000162961 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1433664625 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569498 RMVar_hsa_circ_90738,RMVar_hsa_circ_109614,RMVar_hsa_circ_107570,RMVar_hsa_circ_198248,RMVar_hsa_circ_198249,RMVar_hsa_circ_198250 18880 RMVar_ID_18880 Human_SNP_ID_65971886 A-to-I Human chr2 - 32036125 32036125 32036125 AAAAAATTAGCTGGGTATGGTGGTGTGTGCCTATAGTACCAGCTACTCAGGAGACTGAGGTGGGA AAAAAATTAGCTGGGTATGGTGGTGTGTGCCTGTAGTACCAGCTACTCAGGAGACTGAGGTGGGA T C DPY30 Ensembl:ENSG00000162961 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs995577356 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569498 RMVar_hsa_circ_90738,RMVar_hsa_circ_109614,RMVar_hsa_circ_107570,RMVar_hsa_circ_198248,RMVar_hsa_circ_198249,RMVar_hsa_circ_198250 18881 RMVar_ID_18881 Human_SNP_ID_65971904 A-to-I Human chr2 - 32036196 32036196 32036196 AGGTGGGAGGATTCCTTGAATCTAGGAGTTTAAGACCAGCCTGGGCAACATAGTGAGACCCCATC AGGTGGGAGGATTCCTTGAATCTAGGAGTTTAGGACCAGCCTGGGCAACATAGTGAGACCCCATC T C DPY30 Ensembl:ENSG00000162961 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1174576306 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90738,RMVar_hsa_circ_109614,RMVar_hsa_circ_107570,RMVar_hsa_circ_198248,RMVar_hsa_circ_198249,RMVar_hsa_circ_198250 18882 RMVar_ID_18882 Human_SNP_ID_65972708 A-to-I Human chr2 - 32038758 32038758 32038758 CTGTAATCCTATCTGTTCGGGTGGCTGAGGCCAGAGAATCTCTTGAATCTGGAAGACAGGTTGCA CTGTAATCCTATCTGTTCGGGTGGCTGAGGCCGGAGAATCTCTTGAATCTGGAAGACAGGTTGCA T C DPY30 Ensembl:ENSG00000162961 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1267284329 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13858602 RMVar_hsa_circ_90738,RMVar_hsa_circ_109614,RMVar_hsa_circ_107570,RMVar_hsa_circ_198248,RMVar_hsa_circ_198249,RMVar_hsa_circ_198250 18883 RMVar_ID_18883 Human_SNP_ID_65972744 A-to-I Human chr2 - 32038923 32038923 32038923 AAACCCTTCGCCGGGCGCGATGGCCCACGCCTATCATCCCAGCACTTTGGGAGGCCAAGGCTGGC AAACCCTTCGCCGGGCGCGATGGCCCACGCCTGTCATCCCAGCACTTTGGGAGGCCAAGGCTGGC T C DPY30 Ensembl:ENSG00000162961 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs766988303 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24377178 RMVar_hsa_circ_90738,RMVar_hsa_circ_109614,RMVar_hsa_circ_107570,RMVar_hsa_circ_198248,RMVar_hsa_circ_198249,RMVar_hsa_circ_198250 18884 RMVar_ID_18884 Human_SNP_ID_65984737 A-to-I Human chr2 + 32078529 32078529 32078529 AATATTAGCCCAGTGTAGTGGTGCATGTCTCTAGTCCCAGCTACTCAGAAGGCTGAAGTGAAAGG AATATTAGCCCAGTGTAGTGGTGCATGTCTCTGGTCCCAGCTACTCAGAAGGCTGAAGTGAAAGG A G SPAST Ensembl:ENSG00000021574 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1419558210 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94467,RMVar_hsa_circ_198253 18885 RMVar_ID_18885 Human_SNP_ID_65996467 A-to-I Human chr2 + 32114043 32114043 32114043 TCGGCTCACTTCAACCTCTGACTCCGTGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCAGGTAGC TCGGCTCACTTCAACCTCTGACTCCGTGGTTCCAGCAATTCTCCTGCCTCAGCCTCCCAGGTAGC A C SPAST Ensembl:ENSG00000021574 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251634404 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13268,RMVar_hsa_circ_21297,RMVar_hsa_circ_340906,RMVar_hsa_circ_94467,RMVar_hsa_circ_198253,RMVar_hsa_circ_305073,RMVar_hsa_circ_67201,RMVar_hsa_circ_40142,RMVar_hsa_circ_198259,RMVar_hsa_circ_198256,RMVar_hsa_circ_198257,RMVar_hsa_circ_198258,RMVar_hsa_circ_340118,RMVar_hsa_circ_73976,RMVar_hsa_circ_280264,RMVar_hsa_circ_23584,RMVar_hsa_circ_198263,RMVar_hsa_circ_291555,RMVar_hsa_circ_331539,RMVar_hsa_circ_338932,RMVar_hsa_circ_302590,RMVar_hsa_circ_284648,RMVar_hsa_circ_95454,RMVar_hsa_circ_112329,RMVar_hsa_circ_52498,RMVar_hsa_circ_198274,RMVar_hsa_circ_198265,RMVar_hsa_circ_198267,RMVar_hsa_circ_198269,RMVar_hsa_circ_198270,RMVar_hsa_circ_198268,RMVar_hsa_circ_198266,RMVar_hsa_circ_198272,RMVar_hsa_circ_198264,RMVar_hsa_circ_198271,RMVar_hsa_circ_198275,RMVar_hsa_circ_198273 18886 RMVar_ID_18886 Human_SNP_ID_66006876 A-to-I Human chr2 + 32151868 32151868 32151868 GGGAGGTGGAGGTTGCAGTGAGCTGAGATCGTACCACTGCACTCCAGTCTGTGCGACAGGAGCGA GGGAGGTGGAGGTTGCAGTGAGCTGAGATCGTCCCACTGCACTCCAGTCTGTGCGACAGGAGCGA A C SPAST Ensembl:ENSG00000021574 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1412743628 Functional Loss SNV dbSNP153 33..33 33 - - - 18887 RMVar_ID_18887 Human_SNP_ID_66006877 A-to-I Human chr2 + 32151868 32151868 32151868 GGGAGGTGGAGGTTGCAGTGAGCTGAGATCGTACCACTGCACTCCAGTCTGTGCGACAGGAGCGA GGGAGGTGGAGGTTGCAGTGAGCTGAGATCGTGCCACTGCACTCCAGTCTGTGCGACAGGAGCGA A G SPAST Ensembl:ENSG00000021574 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1412743628 Functional Loss SNV dbSNP153 33..33 33 - - - 18888 RMVar_ID_18888 Human_SNP_ID_66008472 A-to-I Human chr2 - 32157919 32157919 32157919 TTTTTTTTTTGGCAGAAACAGGGTCTCCCTATATTCCCCAGGCTGGTCTTGAATTCCTGAGTGTA TTTTTTTTTTGGCAGAAACAGGGTCTCCCTATTTTCCCCAGGCTGGTCTTGAATTCCTGAGTGTA T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs938390222 Functional Loss SNV dbSNP153 33..33 33 - - - 18889 RMVar_ID_18889 Human_SNP_ID_66014122 A-to-I Human chr2 + 32177247 32177247 32177247 CTGGACATGTCATATAAGTGGAATCATACAATATACAGTCCTTTATGACTGTCTTCTTAGCACAA CTGGACATGTCATATAAGTGGAATCATACAATGTACAGTCCTTTATGACTGTCTTCTTAGCACAA A G SLC30A6 Ensembl:ENSG00000152683 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs889773134 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_283701,RMVar_hsa_circ_341621,RMVar_hsa_circ_6276,RMVar_hsa_circ_15613,RMVar_hsa_circ_38520,RMVar_hsa_circ_198297,RMVar_hsa_circ_267835,RMVar_hsa_circ_289412,RMVar_hsa_circ_318725,RMVar_hsa_circ_370122,RMVar_hsa_circ_268828,RMVar_hsa_circ_16231,RMVar_hsa_circ_198299,RMVar_hsa_circ_198301,RMVar_hsa_circ_198302,RMVar_hsa_circ_198300,RMVar_hsa_circ_20267,RMVar_hsa_circ_198298 18890 RMVar_ID_18890 Human_SNP_ID_66014175 A-to-I Human chr2 + 32177436 32177436 32177436 CCTCAGCCTCCCAAGTAGCTGGGATTACAGGCATGTACCACCAGGCACGGCTAATTTTTTGTATT CCTCAGCCTCCCAAGTAGCTGGGATTACAGGCGTGTACCACCAGGCACGGCTAATTTTTTGTATT A G SLC30A6 Ensembl:ENSG00000152683 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs750104477 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_283701,RMVar_hsa_circ_341621,RMVar_hsa_circ_6276,RMVar_hsa_circ_15613,RMVar_hsa_circ_38520,RMVar_hsa_circ_198297,RMVar_hsa_circ_267835,RMVar_hsa_circ_289412,RMVar_hsa_circ_318725,RMVar_hsa_circ_370122,RMVar_hsa_circ_268828,RMVar_hsa_circ_16231,RMVar_hsa_circ_198299,RMVar_hsa_circ_198301,RMVar_hsa_circ_198302,RMVar_hsa_circ_198300,RMVar_hsa_circ_20267,RMVar_hsa_circ_198298 18891 RMVar_ID_18891 Human_SNP_ID_66015399 A-to-I Human chr2 + 32181729 32181729 32181729 TCTCTACTAAAATACCAAAAAATGAGGTGGGCATGGTGGCGCACTTTTGTAATCCCAGCTGCTTG TCTCTACTAAAATACCAAAAAATGAGGTGGGCGTGGTGGCGCACTTTTGTAATCCCAGCTGCTTG A G SLC30A6 Ensembl:ENSG00000152683 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1406726546 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_283701,RMVar_hsa_circ_341621,RMVar_hsa_circ_80171,RMVar_hsa_circ_6276,RMVar_hsa_circ_15613,RMVar_hsa_circ_38520,RMVar_hsa_circ_198297,RMVar_hsa_circ_267835,RMVar_hsa_circ_289412,RMVar_hsa_circ_318725,RMVar_hsa_circ_370122,RMVar_hsa_circ_268828,RMVar_hsa_circ_16231,RMVar_hsa_circ_198299,RMVar_hsa_circ_198301,RMVar_hsa_circ_198302,RMVar_hsa_circ_198300,RMVar_hsa_circ_20267,RMVar_hsa_circ_198298,RMVar_hsa_circ_121668,RMVar_hsa_circ_198304,RMVar_hsa_circ_198305 18892 RMVar_ID_18892 Human_SNP_ID_66015568 A-to-I Human chr2 + 32182197 32182197 32182197 GCTCTCAAGTGATCCACCTGCCCTGACCTCCCAAAGTGCTAGGTTTACAGGCATGAGCCACCACG GCTCTCAAGTGATCCACCTGCCCTGACCTCCCGAAGTGCTAGGTTTACAGGCATGAGCCACCACG A G SLC30A6 Ensembl:ENSG00000152683 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1244552605 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_283701,RMVar_hsa_circ_341621,RMVar_hsa_circ_80171,RMVar_hsa_circ_6276,RMVar_hsa_circ_15613,RMVar_hsa_circ_38520,RMVar_hsa_circ_198297,RMVar_hsa_circ_267835,RMVar_hsa_circ_289412,RMVar_hsa_circ_318725,RMVar_hsa_circ_370122,RMVar_hsa_circ_268828,RMVar_hsa_circ_16231,RMVar_hsa_circ_198299,RMVar_hsa_circ_198301,RMVar_hsa_circ_198302,RMVar_hsa_circ_198300,RMVar_hsa_circ_20267,RMVar_hsa_circ_198298,RMVar_hsa_circ_121668,RMVar_hsa_circ_198304,RMVar_hsa_circ_198305 18893 RMVar_ID_18893 Human_SNP_ID_66015571 A-to-I Human chr2 + 32182205 32182205 32182205 GTGATCCACCTGCCCTGACCTCCCAAAGTGCTAGGTTTACAGGCATGAGCCACCACGCCCAGCCT GTGATCCACCTGCCCTGACCTCCCAAAGTGCTGGGTTTACAGGCATGAGCCACCACGCCCAGCCT A G SLC30A6 Ensembl:ENSG00000152683 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1273424628 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_283701,RMVar_hsa_circ_341621,RMVar_hsa_circ_80171,RMVar_hsa_circ_6276,RMVar_hsa_circ_15613,RMVar_hsa_circ_38520,RMVar_hsa_circ_198297,RMVar_hsa_circ_267835,RMVar_hsa_circ_289412,RMVar_hsa_circ_318725,RMVar_hsa_circ_370122,RMVar_hsa_circ_268828,RMVar_hsa_circ_16231,RMVar_hsa_circ_198299,RMVar_hsa_circ_198301,RMVar_hsa_circ_198302,RMVar_hsa_circ_198300,RMVar_hsa_circ_20267,RMVar_hsa_circ_198298,RMVar_hsa_circ_121668,RMVar_hsa_circ_198304,RMVar_hsa_circ_198305 18894 RMVar_ID_18894 Human_SNP_ID_66017671 A-to-I Human chr2 + 32189708 32189708 32189708 ATAGCTCATTGCAGCCTTCAACACCTGGGCTCAAGTGGCTCTCCTGCCTCAGCCTCCTGAGTTGC ATAGCTCATTGCAGCCTTCAACACCTGGGCTCCAGTGGCTCTCCTGCCTCAGCCTCCTGAGTTGC A C SLC30A6 Ensembl:ENSG00000152683 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1458366136 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_341621,RMVar_hsa_circ_80171,RMVar_hsa_circ_6276,RMVar_hsa_circ_15613,RMVar_hsa_circ_38520,RMVar_hsa_circ_267835,RMVar_hsa_circ_318725,RMVar_hsa_circ_370122,RMVar_hsa_circ_268828,RMVar_hsa_circ_16231,RMVar_hsa_circ_198299,RMVar_hsa_circ_198301,RMVar_hsa_circ_198300,RMVar_hsa_circ_198298,RMVar_hsa_circ_198307,RMVar_hsa_circ_198305,RMVar_hsa_circ_288519,RMVar_hsa_circ_320573,RMVar_hsa_circ_326326,RMVar_hsa_circ_72242,RMVar_hsa_circ_198306 18895 RMVar_ID_18895 Human_SNP_ID_66021899 A-to-I Human chr2 + 32204998 32204998 32204998 CACACCCAGCTAATTTTTAAAAATATTTGTAGAGATGGGCTCTCACTATGTTGCCCAGGCTGATC CACACCCAGCTAATTTTTAAAAATATTTGTAGCGATGGGCTCTCACTATGTTGCCCAGGCTGATC A C SLC30A6 Ensembl:ENSG00000152683 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1458075691 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267835,RMVar_hsa_circ_16231,RMVar_hsa_circ_198298,RMVar_hsa_circ_198307,RMVar_hsa_circ_326326,RMVar_hsa_circ_72242,RMVar_hsa_circ_298327,RMVar_hsa_circ_341516,RMVar_hsa_circ_198309,RMVar_hsa_circ_291429,RMVar_hsa_circ_306178,RMVar_hsa_circ_198311,RMVar_hsa_circ_198312,RMVar_hsa_circ_332711,RMVar_hsa_circ_276003,RMVar_hsa_circ_334547,RMVar_hsa_circ_36049,RMVar_hsa_circ_198314,RMVar_hsa_circ_198313,RMVar_hsa_circ_316618,RMVar_hsa_circ_343239 18896 RMVar_ID_18896 Human_SNP_ID_66021949 A-to-I Human chr2 + 32205165 32205165 32205165 TTTTTTGGCCAGGAGAGGTGGCTCACGCTTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGCAG TTTTTTGGCCAGGAGAGGTGGCTCACGCTTGTTATCCCAGCACTTTGGGAGGCCAAGGCGGGCAG A T SLC30A6 Ensembl:ENSG00000152683 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1034341754 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267835,RMVar_hsa_circ_16231,RMVar_hsa_circ_198298,RMVar_hsa_circ_198307,RMVar_hsa_circ_326326,RMVar_hsa_circ_72242,RMVar_hsa_circ_298327,RMVar_hsa_circ_341516,RMVar_hsa_circ_198309,RMVar_hsa_circ_291429,RMVar_hsa_circ_306178,RMVar_hsa_circ_198311,RMVar_hsa_circ_198312,RMVar_hsa_circ_332711,RMVar_hsa_circ_276003,RMVar_hsa_circ_334547,RMVar_hsa_circ_36049,RMVar_hsa_circ_198314,RMVar_hsa_circ_198313,RMVar_hsa_circ_316618,RMVar_hsa_circ_343239 18897 RMVar_ID_18897 Human_SNP_ID_66022174 A-to-I Human chr2 + 32205780 32205776 32205781 ACCTTTGCTTCCTGGGTTCAAGCGATTCTCCTACCTCAGCATCCCGAGTAGCTGGGACTACAGCC ACCTTTGCTTCCTGGGTTCAAGCGATTCT_____CTCAGCATCCCGAGTAGCTGGGACTACAGCC TCCTAC T SLC30A6 Ensembl:ENSG00000152683 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1487883842 Functional Loss DEL dbSNP153 30..34 33 - - - RMVar_hsa_circ_267835,RMVar_hsa_circ_16231,RMVar_hsa_circ_198298,RMVar_hsa_circ_198307,RMVar_hsa_circ_326326,RMVar_hsa_circ_72242,RMVar_hsa_circ_298327,RMVar_hsa_circ_341516,RMVar_hsa_circ_198309,RMVar_hsa_circ_291429,RMVar_hsa_circ_306178,RMVar_hsa_circ_198311,RMVar_hsa_circ_198312,RMVar_hsa_circ_332711,RMVar_hsa_circ_276003,RMVar_hsa_circ_334547,RMVar_hsa_circ_36049,RMVar_hsa_circ_198314,RMVar_hsa_circ_198313,RMVar_hsa_circ_316618,RMVar_hsa_circ_343239 18898 RMVar_ID_18898 Human_SNP_ID_66028915 A-to-I Human chr2 + 32228908 32228908 32228908 GCCAACTCAGCTTCCCGTATAGCTGGGATTATAAGTATGTGCACTACGCCCAGCTAATTTTTGTA GCCAACTCAGCTTCCCGTATAGCTGGGATTATGAGTATGTGCACTACGCCCAGCTAATTTTTGTA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1442406405 Functional Loss SNV dbSNP153 33..33 33 - - - 18899 RMVar_ID_18899 Human_SNP_ID_66030551 A-to-I Human chr2 + 32234331 32234331 32234331 ATGAACTAGGGAGGTGGAGTGTGCAGTGAGCTAAGATTGCGCAACTGCACTCCAGCCTGGGCGAC ATGAACTAGGGAGGTGGAGTGTGCAGTGAGCTCAGATTGCGCAACTGCACTCCAGCCTGGGCGAC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404545958 Functional Loss SNV dbSNP153 33..33 33 - - - 18900 RMVar_ID_18900 Human_SNP_ID_66040648 A-to-I Human chr2 + 32270034 32270034 32270034 ACTAAAAAAAAAAAAAAATCGAAAAATTAGCCAGGCATGGGGGTGCATGTCTGGAAACCCAGCTA ACTAAAAAAAAAAAAAAATCGAAAAATTAGCCGGGCATGGGGGTGCATGTCTGGAAACCCAGCTA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1306715230 Functional Loss SNV dbSNP153 33..33 33 - - - 18901 RMVar_ID_18901 Human_SNP_ID_66046036 A-to-I Human chr2 + 32287061 32287061 32287061 GAGGCCAGGAGTTCAGGACCAGACTGGCCAACATGTTGAAACCCCATCTCTACTAAAAATACAAA GAGGCCAGGAGTTCAGGACCAGACTGGCCAACGTGTTGAAACCCCATCTCTACTAAAAATACAAA A G YIPF4 Ensembl:ENSG00000119820 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1020594948 Functional Loss SNV dbSNP153 33..33 33 - - - 18902 RMVar_ID_18902 Human_SNP_ID_66048911 A-to-I Human chr2 + 32295743 32295743 32295743 CTTCTGCCTCAGCCTCCTACATAGCTGGGATTACAGACATGCCCCACCACCCCCAGCTAATTTTG CTTCTGCCTCAGCCTCCTACATAGCTGGGATTGCAGACATGCCCCACCACCCCCAGCTAATTTTG A G YIPF4 Ensembl:ENSG00000119820 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1361902661 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_304613,RMVar_hsa_circ_332898,RMVar_hsa_circ_198319,RMVar_hsa_circ_198320,RMVar_hsa_circ_198318,RMVar_hsa_circ_198321,RMVar_hsa_circ_282526 18903 RMVar_ID_18903 Human_SNP_ID_66049779 A-to-I Human chr2 + 32298688 32298688 32298688 GTTCCCGATTGTCCTGCCTCAGCCTTCCGAGTAGCTGGGATTATAGATATGTGCCACTATGCCCG GTTCCCGATTGTCCTGCCTCAGCCTTCCGAGTGGCTGGGATTATAGATATGTGCCACTATGCCCG A G YIPF4 Ensembl:ENSG00000119820 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs922686743 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_304613,RMVar_hsa_circ_198319,RMVar_hsa_circ_198320,RMVar_hsa_circ_198322,RMVar_hsa_circ_198321,RMVar_hsa_circ_282526,RMVar_hsa_circ_198323,RMVar_hsa_circ_289120 18904 RMVar_ID_18904 Human_SNP_ID_66049784 A-to-I Human chr2 + 32298698 32298698 32298698 GTCCTGCCTCAGCCTTCCGAGTAGCTGGGATTATAGATATGTGCCACTATGCCCGGCTAATTTTT GTCCTGCCTCAGCCTTCCGAGTAGCTGGGATTGTAGATATGTGCCACTATGCCCGGCTAATTTTT A G YIPF4 Ensembl:ENSG00000119820 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1206148425 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25588246 RMVar_hsa_circ_304613,RMVar_hsa_circ_198319,RMVar_hsa_circ_198320,RMVar_hsa_circ_198322,RMVar_hsa_circ_198321,RMVar_hsa_circ_282526,RMVar_hsa_circ_198323,RMVar_hsa_circ_289120 18905 RMVar_ID_18905 Human_SNP_ID_66051135 A-to-I Human chr2 + 32303434 32303434 32303434 TGTTATTACAAATATTATAAAATAGGCCAGGTATGGTGGCTTACTGTTGTAAATCCCAGCAGTTT TGTTATTACAAATATTATAAAATAGGCCAGGTGTGGTGGCTTACTGTTGTAAATCCCAGCAGTTT A G YIPF4 Ensembl:ENSG00000119820 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1303823122 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_198320,RMVar_hsa_circ_198323 18906 RMVar_ID_18906 Human_SNP_ID_66052201 A-to-I Human chr2 + 32307630 32307630 32307630 TGAGCAAAGTAGTTAGAACAGATTGTCAGTTTAAAAACAGGATTTGTAGGCCAGGCACAGTGGCT TGAGCAAAGTAGTTAGAACAGATTGTCAGTTTCAAAACAGGATTTGTAGGCCAGGCACAGTGGCT A C YIPF4 Ensembl:ENSG00000119820 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1453029207 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1300769,Human_RBP_ID_2638349,Human_RBP_ID_6911959,Human_RBP_ID_8847816,Human_RBP_ID_13861145,Human_RBP_ID_17955750,Human_RBP_ID_26486332 18907 RMVar_ID_18907 Human_SNP_ID_66052212 A-to-I Human chr2 + 32307672 32307672 32307672 TTTGTAGGCCAGGCACAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAAGTGGATGA TTTGTAGGCCAGGCACAGTGGCTCACGCCTGTCATCCCAGCACTTTGGGAGGCCAAAGTGGATGA A C YIPF4 Ensembl:ENSG00000119820 Protein coding 3'UTR GSE38233;GSE100210;GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,29129909,30559470,31158229,31158229 RNA-Seq:(High) rs1302329410 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26487083 18908 RMVar_ID_18908 Human_SNP_ID_66052213 A-to-I Human chr2 + 32307678 32307678 32307678 GGCCAGGCACAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAAGTGGATGAGCAGCT GGCCAGGCACAGTGGCTCACGCCTGTAATCCCGGCACTTTGGGAGGCCAAAGTGGATGAGCAGCT A G YIPF4 Ensembl:ENSG00000119820 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs909589339 Functional Loss SNV dbSNP153 33..33 33 - - - 18909 RMVar_ID_18909 Human_SNP_ID_66052217 A-to-I Human chr2 + 32307695 32307695 32307695 CACGCCTGTAATCCCAGCACTTTGGGAGGCCAAAGTGGATGAGCAGCTTGAGTCAGGAGTTTGAG CACGCCTGTAATCCCAGCACTTTGGGAGGCCAGAGTGGATGAGCAGCTTGAGTCAGGAGTTTGAG A G YIPF4 Ensembl:ENSG00000119820 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs958928624 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9105680,Human_RBP_ID_13861151,Human_RBP_ID_22595030 18910 RMVar_ID_18910 Human_SNP_ID_66052227 A-to-I Human chr2 + 32307740 32307740 32307740 GCTTGAGTCAGGAGTTTGAGACCAGCCTGGCCAACATGGCGAAACCCCGTCTCTACTAAAAATAC GCTTGAGTCAGGAGTTTGAGACCAGCCTGGCCGACATGGCGAAACCCCGTCTCTACTAAAAATAC A G YIPF4 Ensembl:ENSG00000119820 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1137922 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9105680 18911 RMVar_ID_18911 Human_SNP_ID_66052233 A-to-I Human chr2 + 32307750 32307750 32307750 GGAGTTTGAGACCAGCCTGGCCAACATGGCGAAACCCCGTCTCTACTAAAAATACAAAAATTAGC GGAGTTTGAGACCAGCCTGGCCAACATGGCGACACCCCGTCTCTACTAAAAATACAAAAATTAGC A C YIPF4 Ensembl:ENSG00000119820 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1279370957 Functional Loss SNV dbSNP153 33..33 33 - - - 18912 RMVar_ID_18912 Human_SNP_ID_66052415 A-to-I Human chr2 + 32308275 32308275 32308275 GGGACTACAGGCGCCCACCACCATGCCTGGCTAATTTTTTGTATTTTTAGTAGAGATGGGGTTTC GGGACTACAGGCGCCCACCACCATGCCTGGCTGATTTTTTGTATTTTTAGTAGAGATGGGGTTTC A G YIPF4 Ensembl:ENSG00000119820 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs754602167 Functional Loss SNV dbSNP153 33..33 33 - - - 18913 RMVar_ID_18913 Human_SNP_ID_66052446 A-to-I Human chr2 + 32308361 32308361 32308361 TCGATCTCCTGACCTCGTGATCCGCCCGCCTCAGCCTCCCAAAGTGCCGGGATTACAGGTGTCAG TCGATCTCCTGACCTCGTGATCCGCCCGCCTCTGCCTCCCAAAGTGCCGGGATTACAGGTGTCAG A T YIPF4 Ensembl:ENSG00000119820 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1171647705 Functional Loss SNV dbSNP153 33..33 33 - - - 18914 RMVar_ID_18914 Human_SNP_ID_66052447 A-to-I Human chr2 + 32308370 32308370 32308370 TGACCTCGTGATCCGCCCGCCTCAGCCTCCCAAAGTGCCGGGATTACAGGTGTCAGCCACCGCAC TGACCTCGTGATCCGCCCGCCTCAGCCTCCCAGAGTGCCGGGATTACAGGTGTCAGCCACCGCAC A G YIPF4 Ensembl:ENSG00000119820 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1489106848 Functional Loss SNV dbSNP153 33..33 33 - - - 18915 RMVar_ID_18915 Human_SNP_ID_66052483 A-to-I Human chr2 + 32308485 32308485 32308485 CCTGTAATCCCAGCAGTTTGGGAGGCCGAGGCAGGTGGATCACCTGAGGTTGGGAGTTTGAGACC CCTGTAATCCCAGCAGTTTGGGAGGCCGAGGCGGGTGGATCACCTGAGGTTGGGAGTTTGAGACC A G YIPF4 Ensembl:ENSG00000119820 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1312827325 Functional Loss SNV dbSNP153 33..33 33 - - - 18916 RMVar_ID_18916 Human_SNP_ID_66052856 A-to-I Human chr2 + 32309752 32309752 32309752 TGCTCTCTCGCCCAGGCTGGAGTGTGTGGCGCAATCTCAGCTCACTGCAACCTCTGATTCCTGGG TGCTCTCTCGCCCAGGCTGGAGTGTGTGGCGCTATCTCAGCTCACTGCAACCTCTGATTCCTGGG A T YIPF4 Ensembl:ENSG00000119820 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1210856752 Functional Loss SNV dbSNP153 33..33 33 - - - 18917 RMVar_ID_18917 Human_SNP_ID_66052862 A-to-I Human chr2 + 32309763 32309763 32309763 CCAGGCTGGAGTGTGTGGCGCAATCTCAGCTCACTGCAACCTCTGATTCCTGGGTTCAAGCAATT CCAGGCTGGAGTGTGTGGCGCAATCTCAGCTCCCTGCAACCTCTGATTCCTGGGTTCAAGCAATT A C YIPF4 Ensembl:ENSG00000119820 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs993704480 Functional Loss SNV dbSNP153 33..33 33 - - - 18918 RMVar_ID_18918 Human_SNP_ID_66052875 A-to-I Human chr2 + 32309822 32309822 32309822 GCAATTCTCATGTCTCAGCCTCCCTAATAGCTAGGATTACCGGTGCCCGCCACCACGCCCAGCTA GCAATTCTCATGTCTCAGCCTCCCTAATAGCTGGGATTACCGGTGCCCGCCACCACGCCCAGCTA A G YIPF4 Ensembl:ENSG00000119820 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs188590505 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25534793 18919 RMVar_ID_18919 Human_SNP_ID_66052895 A-to-I Human chr2 + 32309879 32309879 32309879 CCCAGCTAATTTTTTAAATTTTTAATGGAGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTTAA CCCAGCTAATTTTTTAAATTTTTAATGGAGACGGGGTTTCACCATGTTGGCCAGGCTGGTCTTAA A G YIPF4 Ensembl:ENSG00000119820 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1301195353 Functional Loss SNV dbSNP153 33..33 33 - - - 18920 RMVar_ID_18920 Human_SNP_ID_66053098 A-to-I Human chr2 + 32310616 32310616 32310616 AAAATTGTTTGTATGCCTGGGTACAGTATCATACCTGTAATCCCAGCACTTTGGAAGGCTGAGGC AAAATTGTTTGTATGCCTGGGTACAGTATCATGCCTGTAATCCCAGCACTTTGGAAGGCTGAGGC A G YIPF4 Ensembl:ENSG00000119820 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1376735703 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17507307,Human_RBP_ID_17570667 18921 RMVar_ID_18921 Human_SNP_ID_66053115 A-to-I Human chr2 + 32310677 32310676 32310677 AGGCGGGAGGACTGTTTTGTGGCCAGGAGTTCAAAATCAGCCTGGTCGACGTAGTGAGACCCCAT AGGCGGGAGGACTGTTTTGTGGCCAGGAGTTC_AAATCAGCCTGGTCGACGTAGTGAGACCCCAT CA C YIPF4 Ensembl:ENSG00000119820 Protein coding 3'UTR GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,30559470,31158229,31158229,31158229,31158229,31158229 RNA-Seq:(High) rs1305996176 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_6911988,Human_RBP_ID_17569504 18922 RMVar_ID_18922 Human_SNP_ID_66053123 A-to-I Human chr2 + 32310697 32310697 32310697 GGCCAGGAGTTCAAAATCAGCCTGGTCGACGTAGTGAGACCCCATCTCTACAAAAGAAAAATTAG GGCCAGGAGTTCAAAATCAGCCTGGTCGACGTCGTGAGACCCCATCTCTACAAAAGAAAAATTAG A C YIPF4 Ensembl:ENSG00000119820 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1400970102 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6911988,Human_RBP_ID_13861183,Human_RBP_ID_17569504 18923 RMVar_ID_18923 Human_SNP_ID_66053126 A-to-I Human chr2 + 32310708 32310708 32310708 CAAAATCAGCCTGGTCGACGTAGTGAGACCCCATCTCTACAAAAGAAAAATTAGCTGGGCATGTG CAAAATCAGCCTGGTCGACGTAGTGAGACCCCGTCTCTACAAAAGAAAAATTAGCTGGGCATGTG A G YIPF4 Ensembl:ENSG00000119820 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1054535462 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6911988,Human_RBP_ID_13861184,Human_RBP_ID_17569504 18924 RMVar_ID_18924 Human_SNP_ID_66054047 A-to-I Human chr2 + 32313640 32313640 32313640 TGCCCACCTCAACCTCCCAAAGTGCTGGGATTACAGGCGTGAGACACTGTGCCCAGCCTGTCAGA TGCCCACCTCAACCTCCCAAAGTGCTGGGATTTCAGGCGTGAGACACTGTGCCCAGCCTGTCAGA A T YIPF4 Ensembl:ENSG00000119820 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1488905895 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23182657 18925 RMVar_ID_18925 Human_SNP_ID_66059765 A-to-I Human chr2 + 32333938 32333938 32333938 TTTGAGACAGGGCTCACTCTGTTGCCCAAGCTAGAGTACAGTGGCATGATCATGACTCACTACAG TTTGAGACAGGGCTCACTCTGTTGCCCAAGCTGGAGTACAGTGGCATGATCATGACTCACTACAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017098897 Functional Loss SNV dbSNP153 33..33 33 - - - 18926 RMVar_ID_18926 Human_SNP_ID_66069325 A-to-I Human chr2 + 32367695 32367695 32367695 AAAATTAGCTGGGTGTGGTGGTGTACACTTGTAATTCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTAGCTGGGTGTGGTGGTGTACACTTGTCATTCCAGCTACTCGGGAGGCTGAGGCAGGAGA A C BIRC6 Ensembl:ENSG00000115760 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973017838 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99265,RMVar_hsa_circ_107874,RMVar_hsa_circ_113509,RMVar_hsa_circ_104141,RMVar_hsa_circ_198324,RMVar_hsa_circ_198326,RMVar_hsa_circ_198327,RMVar_hsa_circ_198325 18927 RMVar_ID_18927 Human_SNP_ID_66069603 A-to-I Human chr2 + 32368726 32368726 32368726 CAGGCTGGAGTGCAGTGGTGTGATCTCAGCTCACTTCAACGTCTTCCTCCTGGGTTCAAGTGATT CAGGCTGGAGTGCAGTGGTGTGATCTCAGCTCGCTTCAACGTCTTCCTCCTGGGTTCAAGTGATT A G BIRC6 Ensembl:ENSG00000115760 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1282866062 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99265,RMVar_hsa_circ_107874,RMVar_hsa_circ_113509,RMVar_hsa_circ_104141,RMVar_hsa_circ_198324,RMVar_hsa_circ_198326,RMVar_hsa_circ_198327,RMVar_hsa_circ_198325 18928 RMVar_ID_18928 Human_SNP_ID_66069638 A-to-I Human chr2 + 32368823 32368823 32368823 ACAGGTGTGTACCACCATGCCCAGCTAATTTTAGTACTTTTAATAGAGACAAGGTTTCACCATGT ACAGGTGTGTACCACCATGCCCAGCTAATTTTTGTACTTTTAATAGAGACAAGGTTTCACCATGT A T BIRC6 Ensembl:ENSG00000115760 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs955242233 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99265,RMVar_hsa_circ_107874,RMVar_hsa_circ_113509,RMVar_hsa_circ_104141,RMVar_hsa_circ_198324,RMVar_hsa_circ_198326,RMVar_hsa_circ_198327,RMVar_hsa_circ_198325 18929 RMVar_ID_18929 Human_SNP_ID_66071027 A-to-I Human chr2 + 32372731 32372731 32372731 GTGCGCCTGTAGTCCCAGCTACTTGGGAGGCTAAGATGGGAGGATTACCTGAGCCCTGGAGGTCA GTGCGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGATGGGAGGATTACCTGAGCCCTGGAGGTCA A G BIRC6 Ensembl:ENSG00000115760 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1373379060 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99265,RMVar_hsa_circ_107874,RMVar_hsa_circ_113509,RMVar_hsa_circ_104141,RMVar_hsa_circ_198324,RMVar_hsa_circ_198326,RMVar_hsa_circ_198327,RMVar_hsa_circ_198325 18930 RMVar_ID_18930 Human_SNP_ID_66077893 A-to-I Human chr2 + 32396980 32396980 32396980 GAACTCCTGAGCTCAGGTGATCCACCCACCTCAGCCTTCCGAAGTGTTGGGATTACAGGCGTGAG GAACTCCTGAGCTCAGGTGATCCACCCACCTCCGCCTTCCGAAGTGTTGGGATTACAGGCGTGAG A C BIRC6 Ensembl:ENSG00000115760 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs565892741 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_549844 RMVar_hsa_circ_390,RMVar_hsa_circ_24130,RMVar_hsa_circ_276695,RMVar_hsa_circ_107874,RMVar_hsa_circ_113509,RMVar_hsa_circ_104141,RMVar_hsa_circ_296974,RMVar_hsa_circ_316322,RMVar_hsa_circ_198324,RMVar_hsa_circ_198326,RMVar_hsa_circ_198325,RMVar_hsa_circ_341510,RMVar_hsa_circ_373093,RMVar_hsa_circ_353575,RMVar_hsa_circ_323602,RMVar_hsa_circ_306680,RMVar_hsa_circ_285213,RMVar_hsa_circ_286895,RMVar_hsa_circ_276994,RMVar_hsa_circ_99775,RMVar_hsa_circ_274882,RMVar_hsa_circ_272401,RMVar_hsa_circ_114437,RMVar_hsa_circ_125729,RMVar_hsa_circ_103175,RMVar_hsa_circ_92255,RMVar_hsa_circ_96713,RMVar_hsa_circ_98518,RMVar_hsa_circ_93910,RMVar_hsa_circ_76084,RMVar_hsa_circ_77962,RMVar_hsa_circ_61111,RMVar_hsa_circ_198329,RMVar_hsa_circ_198341,RMVar_hsa_circ_198345,RMVar_hsa_circ_198349,RMVar_hsa_circ_198351,RMVar_hsa_circ_198353,RMVar_hsa_circ_198354,RMVar_hsa_circ_198352,RMVar_hsa_circ_198350,RMVar_hsa_circ_198347,RMVar_hsa_circ_198348,RMVar_hsa_circ_198346,RMVar_hsa_circ_198343,RMVar_hsa_circ_198344,RMVar_hsa_circ_198342,RMVar_hsa_circ_198339,RMVar_hsa_circ_198340,RMVar_hsa_circ_198338,RMVar_hsa_circ_198333,RMVar_hsa_circ_198331,RMVar_hsa_circ_198332,RMVar_hsa_circ_198330,RMVar_hsa_circ_123501,RMVar_hsa_circ_374883,RMVar_hsa_circ_375268,RMVar_hsa_circ_125484,RMVar_hsa_circ_114148,RMVar_hsa_circ_91580,RMVar_hsa_circ_87602,RMVar_hsa_circ_117057,RMVar_hsa_circ_198356,RMVar_hsa_circ_198360,RMVar_hsa_circ_198361,RMVar_hsa_circ_198358,RMVar_hsa_circ_198359,RMVar_hsa_circ_198357,RMVar_hsa_circ_369108,RMVar_hsa_circ_198355,RMVar_hsa_circ_374668,RMVar_hsa_circ_314758,RMVar_hsa_circ_123586,RMVar_hsa_circ_121662,RMVar_hsa_circ_79975,RMVar_hsa_circ_101904,RMVar_hsa_circ_113189,RMVar_hsa_circ_83036,RMVar_hsa_circ_67005,RMVar_hsa_circ_75583,RMVar_hsa_circ_41377,RMVar_hsa_circ_47783,RMVar_hsa_circ_127624,RMVar_hsa_circ_198368,RMVar_hsa_circ_198370,RMVar_hsa_circ_198372,RMVar_hsa_circ_198373,RMVar_hsa_circ_198371,RMVar_hsa_circ_198369,RMVar_hsa_circ_198366,RMVar_hsa_circ_198367,RMVar_hsa_circ_371344,RMVar_hsa_circ_198365,RMVar_hsa_circ_370848,RMVar_hsa_circ_85985,RMVar_hsa_circ_121751,RMVar_hsa_circ_105119,RMVar_hsa_circ_198376,RMVar_hsa_circ_198380,RMVar_hsa_circ_198382,RMVar_hsa_circ_80245,RMVar_hsa_circ_198381,RMVar_hsa_circ_198378,RMVar_hsa_circ_198379,RMVar_hsa_circ_198377,RMVar_hsa_circ_114991,RMVar_hsa_circ_70256,RMVar_hsa_circ_12159,RMVar_hsa_circ_13784,RMVar_hsa_circ_198385 18931 RMVar_ID_18931 Human_SNP_ID_66080789 A-to-I Human chr2 + 32407301 32407301 32407301 AACCCCGTTTCTACTAAAAATAAAAAACAATTAGCCAGGCGTGGTGGCGCATGCCTATCCCAGTT AACCCCGTTTCTACTAAAAATAAAAAACAATTTGCCAGGCGTGGTGGCGCATGCCTATCCCAGTT A T BIRC6 Ensembl:ENSG00000115760 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7605185 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24130,RMVar_hsa_circ_276695,RMVar_hsa_circ_107874,RMVar_hsa_circ_104141,RMVar_hsa_circ_296974,RMVar_hsa_circ_316322,RMVar_hsa_circ_198324,RMVar_hsa_circ_198325,RMVar_hsa_circ_341510,RMVar_hsa_circ_373093,RMVar_hsa_circ_353575,RMVar_hsa_circ_323602,RMVar_hsa_circ_306680,RMVar_hsa_circ_286895,RMVar_hsa_circ_99775,RMVar_hsa_circ_272401,RMVar_hsa_circ_114437,RMVar_hsa_circ_125729,RMVar_hsa_circ_103175,RMVar_hsa_circ_92255,RMVar_hsa_circ_96713,RMVar_hsa_circ_98518,RMVar_hsa_circ_93910,RMVar_hsa_circ_76084,RMVar_hsa_circ_77962,RMVar_hsa_circ_61111,RMVar_hsa_circ_198329,RMVar_hsa_circ_198341,RMVar_hsa_circ_198345,RMVar_hsa_circ_198349,RMVar_hsa_circ_198351,RMVar_hsa_circ_198353,RMVar_hsa_circ_198354,RMVar_hsa_circ_198352,RMVar_hsa_circ_198350,RMVar_hsa_circ_198347,RMVar_hsa_circ_198348,RMVar_hsa_circ_198346,RMVar_hsa_circ_198343,RMVar_hsa_circ_198344,RMVar_hsa_circ_198342,RMVar_hsa_circ_198333,RMVar_hsa_circ_198331,RMVar_hsa_circ_198332,RMVar_hsa_circ_198330,RMVar_hsa_circ_123501,RMVar_hsa_circ_125484,RMVar_hsa_circ_114148,RMVar_hsa_circ_91580,RMVar_hsa_circ_117057,RMVar_hsa_circ_198356,RMVar_hsa_circ_198358,RMVar_hsa_circ_198357,RMVar_hsa_circ_369108,RMVar_hsa_circ_198355,RMVar_hsa_circ_374668,RMVar_hsa_circ_121662,RMVar_hsa_circ_79975,RMVar_hsa_circ_101904,RMVar_hsa_circ_113189,RMVar_hsa_circ_83036,RMVar_hsa_circ_67005,RMVar_hsa_circ_75583,RMVar_hsa_circ_41377,RMVar_hsa_circ_8179,RMVar_hsa_circ_47783,RMVar_hsa_circ_127624,RMVar_hsa_circ_198368,RMVar_hsa_circ_198370,RMVar_hsa_circ_198372,RMVar_hsa_circ_198371,RMVar_hsa_circ_198369,RMVar_hsa_circ_198366,RMVar_hsa_circ_198367,RMVar_hsa_circ_198365,RMVar_hsa_circ_85985,RMVar_hsa_circ_121751,RMVar_hsa_circ_105119,RMVar_hsa_circ_198376,RMVar_hsa_circ_198378,RMVar_hsa_circ_198379,RMVar_hsa_circ_198377,RMVar_hsa_circ_114991,RMVar_hsa_circ_96640,RMVar_hsa_circ_13784,RMVar_hsa_circ_198385,RMVar_hsa_circ_292148,RMVar_hsa_circ_311755,RMVar_hsa_circ_336264,RMVar_hsa_circ_348901,RMVar_hsa_circ_325781,RMVar_hsa_circ_301185,RMVar_hsa_circ_39974,RMVar_hsa_circ_48845,RMVar_hsa_circ_56919,RMVar_hsa_circ_43932,RMVar_hsa_circ_32864,RMVar_hsa_circ_15051,RMVar_hsa_circ_44727,RMVar_hsa_circ_116988,RMVar_hsa_circ_198386,RMVar_hsa_circ_198387,RMVar_hsa_circ_122527,RMVar_hsa_circ_119786,RMVar_hsa_circ_31036,RMVar_hsa_circ_114860,RMVar_hsa_circ_198391,RMVar_hsa_circ_198392,RMVar_hsa_circ_198393,RMVar_hsa_circ_198390,RMVar_hsa_circ_103580,RMVar_hsa_circ_124775,RMVar_hsa_circ_286957,RMVar_hsa_circ_114693,RMVar_hsa_circ_51195,RMVar_hsa_circ_79152,RMVar_hsa_circ_45964,RMVar_hsa_circ_198394,RMVar_hsa_circ_198396,RMVar_hsa_circ_198397,RMVar_hsa_circ_198398,RMVar_hsa_circ_198395 18932 RMVar_ID_18932 Human_SNP_ID_66082835 A-to-I Human chr2 + 32414389 32414389 32414389 AGGGCTGACTGCACTTTAAATTTTTTTAGGCCAGGCGTGGTGGCTCACGCCTGTAATCCCAGCAC AGGGCTGACTGCACTTTAAATTTTTTTAGGCCGGGCGTGGTGGCTCACGCCTGTAATCCCAGCAC A G BIRC6 Ensembl:ENSG00000115760 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1044222229 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24130,RMVar_hsa_circ_276695,RMVar_hsa_circ_107874,RMVar_hsa_circ_104141,RMVar_hsa_circ_296974,RMVar_hsa_circ_316322,RMVar_hsa_circ_198324,RMVar_hsa_circ_198325,RMVar_hsa_circ_341510,RMVar_hsa_circ_373093,RMVar_hsa_circ_353575,RMVar_hsa_circ_323602,RMVar_hsa_circ_306680,RMVar_hsa_circ_286895,RMVar_hsa_circ_99775,RMVar_hsa_circ_272401,RMVar_hsa_circ_114437,RMVar_hsa_circ_125729,RMVar_hsa_circ_103175,RMVar_hsa_circ_92255,RMVar_hsa_circ_96713,RMVar_hsa_circ_98518,RMVar_hsa_circ_93910,RMVar_hsa_circ_76084,RMVar_hsa_circ_77962,RMVar_hsa_circ_61111,RMVar_hsa_circ_198329,RMVar_hsa_circ_198341,RMVar_hsa_circ_198345,RMVar_hsa_circ_198349,RMVar_hsa_circ_198351,RMVar_hsa_circ_198353,RMVar_hsa_circ_198354,RMVar_hsa_circ_198352,RMVar_hsa_circ_198350,RMVar_hsa_circ_198347,RMVar_hsa_circ_198348,RMVar_hsa_circ_198346,RMVar_hsa_circ_198343,RMVar_hsa_circ_198344,RMVar_hsa_circ_198342,RMVar_hsa_circ_198333,RMVar_hsa_circ_198331,RMVar_hsa_circ_198332,RMVar_hsa_circ_198330,RMVar_hsa_circ_123501,RMVar_hsa_circ_125484,RMVar_hsa_circ_114148,RMVar_hsa_circ_91580,RMVar_hsa_circ_117057,RMVar_hsa_circ_198356,RMVar_hsa_circ_198358,RMVar_hsa_circ_198357,RMVar_hsa_circ_369108,RMVar_hsa_circ_198355,RMVar_hsa_circ_374668,RMVar_hsa_circ_121662,RMVar_hsa_circ_79975,RMVar_hsa_circ_101904,RMVar_hsa_circ_113189,RMVar_hsa_circ_83036,RMVar_hsa_circ_67005,RMVar_hsa_circ_75583,RMVar_hsa_circ_41377,RMVar_hsa_circ_8179,RMVar_hsa_circ_47783,RMVar_hsa_circ_127624,RMVar_hsa_circ_198368,RMVar_hsa_circ_198370,RMVar_hsa_circ_198372,RMVar_hsa_circ_198371,RMVar_hsa_circ_198369,RMVar_hsa_circ_198366,RMVar_hsa_circ_198367,RMVar_hsa_circ_198365,RMVar_hsa_circ_85985,RMVar_hsa_circ_121751,RMVar_hsa_circ_105119,RMVar_hsa_circ_198376,RMVar_hsa_circ_198378,RMVar_hsa_circ_198379,RMVar_hsa_circ_198377,RMVar_hsa_circ_114991,RMVar_hsa_circ_96640,RMVar_hsa_circ_13784,RMVar_hsa_circ_198385,RMVar_hsa_circ_292148,RMVar_hsa_circ_311755,RMVar_hsa_circ_336264,RMVar_hsa_circ_348901,RMVar_hsa_circ_325781,RMVar_hsa_circ_301185,RMVar_hsa_circ_39974,RMVar_hsa_circ_48845,RMVar_hsa_circ_56919,RMVar_hsa_circ_43932,RMVar_hsa_circ_32864,RMVar_hsa_circ_15051,RMVar_hsa_circ_44727,RMVar_hsa_circ_116988,RMVar_hsa_circ_198386,RMVar_hsa_circ_198387,RMVar_hsa_circ_122527,RMVar_hsa_circ_119786,RMVar_hsa_circ_31036,RMVar_hsa_circ_114860,RMVar_hsa_circ_198391,RMVar_hsa_circ_198392,RMVar_hsa_circ_198393,RMVar_hsa_circ_198390,RMVar_hsa_circ_103580,RMVar_hsa_circ_124775,RMVar_hsa_circ_286957,RMVar_hsa_circ_114693,RMVar_hsa_circ_51195,RMVar_hsa_circ_79152,RMVar_hsa_circ_45964,RMVar_hsa_circ_198394,RMVar_hsa_circ_198396,RMVar_hsa_circ_198397,RMVar_hsa_circ_198398,RMVar_hsa_circ_198395 18933 RMVar_ID_18933 Human_SNP_ID_66097229 A-to-I Human chr2 + 32462876 32462876 32462876 TACTCAGGAGGCTGAGGCACAAGAATCTCTTGAACCCAGACGTGGAGGTTGCAGTGAACCAAGAT TACTCAGGAGGCTGAGGCACAAGAATCTCTTGGACCCAGACGTGGAGGTTGCAGTGAACCAAGAT A G BIRC6 Ensembl:ENSG00000115760 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs993098465 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13863719,Human_RBP_ID_17569507,Human_RBP_ID_18947727 RMVar_hsa_circ_24130,RMVar_hsa_circ_107874,RMVar_hsa_circ_316322,RMVar_hsa_circ_198324,RMVar_hsa_circ_373093,RMVar_hsa_circ_353575,RMVar_hsa_circ_99775,RMVar_hsa_circ_125729,RMVar_hsa_circ_92255,RMVar_hsa_circ_96713,RMVar_hsa_circ_93910,RMVar_hsa_circ_76084,RMVar_hsa_circ_77962,RMVar_hsa_circ_198329,RMVar_hsa_circ_198351,RMVar_hsa_circ_198353,RMVar_hsa_circ_198354,RMVar_hsa_circ_198352,RMVar_hsa_circ_198333,RMVar_hsa_circ_198331,RMVar_hsa_circ_198332,RMVar_hsa_circ_198330,RMVar_hsa_circ_101904,RMVar_hsa_circ_113189,RMVar_hsa_circ_67005,RMVar_hsa_circ_75583,RMVar_hsa_circ_41377,RMVar_hsa_circ_91445,RMVar_hsa_circ_8179,RMVar_hsa_circ_47783,RMVar_hsa_circ_198366,RMVar_hsa_circ_198367,RMVar_hsa_circ_198365,RMVar_hsa_circ_121751,RMVar_hsa_circ_198376,RMVar_hsa_circ_114991,RMVar_hsa_circ_96640,RMVar_hsa_circ_198385,RMVar_hsa_circ_336264,RMVar_hsa_circ_39974,RMVar_hsa_circ_48845,RMVar_hsa_circ_43932,RMVar_hsa_circ_32864,RMVar_hsa_circ_15051,RMVar_hsa_circ_44727,RMVar_hsa_circ_116988,RMVar_hsa_circ_198386,RMVar_hsa_circ_119786,RMVar_hsa_circ_198392,RMVar_hsa_circ_198393,RMVar_hsa_circ_103580,RMVar_hsa_circ_79152,RMVar_hsa_circ_198394,RMVar_hsa_circ_198395,RMVar_hsa_circ_123363,RMVar_hsa_circ_128061,RMVar_hsa_circ_106349,RMVar_hsa_circ_111981,RMVar_hsa_circ_102690,RMVar_hsa_circ_20626,RMVar_hsa_circ_106651,RMVar_hsa_circ_198402,RMVar_hsa_circ_198404,RMVar_hsa_circ_198403,RMVar_hsa_circ_198400,RMVar_hsa_circ_198401,RMVar_hsa_circ_198399,RMVar_hsa_circ_25859,RMVar_hsa_circ_198411,RMVar_hsa_circ_39789,RMVar_hsa_circ_125367,RMVar_hsa_circ_82363,RMVar_hsa_circ_198422,RMVar_hsa_circ_198424,RMVar_hsa_circ_198421,RMVar_hsa_circ_113159,RMVar_hsa_circ_122434,RMVar_hsa_circ_43315,RMVar_hsa_circ_37466,RMVar_hsa_circ_58033,RMVar_hsa_circ_198426,RMVar_hsa_circ_5923,RMVar_hsa_circ_15822,RMVar_hsa_circ_3181,RMVar_hsa_circ_198425,RMVar_hsa_circ_67650,RMVar_hsa_circ_308133,RMVar_hsa_circ_319915,RMVar_hsa_circ_373734,RMVar_hsa_circ_312338,RMVar_hsa_circ_298488,RMVar_hsa_circ_281409,RMVar_hsa_circ_282937,RMVar_hsa_circ_51154,RMVar_hsa_circ_114028,RMVar_hsa_circ_198439,RMVar_hsa_circ_198441,RMVar_hsa_circ_198442,RMVar_hsa_circ_198440,RMVar_hsa_circ_198438,RMVar_hsa_circ_91866,RMVar_hsa_circ_117108,RMVar_hsa_circ_198446,RMVar_hsa_circ_27815,RMVar_hsa_circ_19237,RMVar_hsa_circ_86732,RMVar_hsa_circ_198449,RMVar_hsa_circ_198450,RMVar_hsa_circ_116121,RMVar_hsa_circ_14687,RMVar_hsa_circ_198454,RMVar_hsa_circ_59127,RMVar_hsa_circ_198455,RMVar_hsa_circ_73350,RMVar_hsa_circ_123519,RMVar_hsa_circ_61078,RMVar_hsa_circ_67556,RMVar_hsa_circ_321798,RMVar_hsa_circ_198456,RMVar_hsa_circ_362690,RMVar_hsa_circ_306125,RMVar_hsa_circ_72112,RMVar_hsa_circ_67324,RMVar_hsa_circ_67418,RMVar_hsa_circ_58388,RMVar_hsa_circ_8510,RMVar_hsa_circ_9810 18934 RMVar_ID_18934 Human_SNP_ID_66109065 A-to-I Human chr2 + 32503905 32503905 32503905 AGTGGTGCTGTGTTTTGTTTTGAGAGAGTCTCACTCTCACCTAGGCTGGAGTGCAGTGGCACAGT AGTGGTGCTGTGTTTTGTTTTGAGAGAGTCTCGCTCTCACCTAGGCTGGAGTGCAGTGGCACAGT A G BIRC6 Ensembl:ENSG00000115760 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1025861161 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6912981,Human_RBP_ID_13864385 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_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_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_198532 18935 RMVar_ID_18935 Human_SNP_ID_66110113 A-to-I Human chr2 + 32507293 32507293 32507293 CTCTACCAAAAGTACAAAAATTACCTAGATGTAGTGGCACCTACCTGTAGTTCCAACTACTCTGG CTCTACCAAAAGTACAAAAATTACCTAGATGTGGTGGCACCTACCTGTAGTTCCAACTACTCTGG A G BIRC6 Ensembl:ENSG00000115760 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs975995574 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13864421 RMVar_hsa_circ_316322,RMVar_hsa_circ_41377,RMVar_hsa_circ_8179,RMVar_hsa_circ_47783,RMVar_hsa_circ_15051,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_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_65955,RMVar_hsa_circ_61053,RMVar_hsa_circ_339840,RMVar_hsa_circ_342878,RMVar_hsa_circ_333176,RMVar_hsa_circ_300566,RMVar_hsa_circ_276088,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_198489,RMVar_hsa_circ_102684,RMVar_hsa_circ_54548,RMVar_hsa_circ_64795,RMVar_hsa_circ_198493,RMVar_hsa_circ_198494,RMVar_hsa_circ_340513,RMVar_hsa_circ_325095,RMVar_hsa_circ_198495,RMVar_hsa_circ_198496,RMVar_hsa_circ_51998,RMVar_hsa_circ_107836,RMVar_hsa_circ_115831,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_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_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_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_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_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_350684,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_198541,RMVar_hsa_circ_198538,RMVar_hsa_circ_198539,RMVar_hsa_circ_198537 18936 RMVar_ID_18936 Human_SNP_ID_66110121 A-to-I Human chr2 + 32507303 32507303 32507303 AGTACAAAAATTACCTAGATGTAGTGGCACCTACCTGTAGTTCCAACTACTCTGGAGGCTACGGC AGTACAAAAATTACCTAGATGTAGTGGCACCTTCCTGTAGTTCCAACTACTCTGGAGGCTACGGC A T BIRC6 Ensembl:ENSG00000115760 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1442080948 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13864421 RMVar_hsa_circ_316322,RMVar_hsa_circ_41377,RMVar_hsa_circ_8179,RMVar_hsa_circ_47783,RMVar_hsa_circ_15051,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_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_65955,RMVar_hsa_circ_61053,RMVar_hsa_circ_339840,RMVar_hsa_circ_342878,RMVar_hsa_circ_333176,RMVar_hsa_circ_300566,RMVar_hsa_circ_276088,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_198489,RMVar_hsa_circ_102684,RMVar_hsa_circ_54548,RMVar_hsa_circ_64795,RMVar_hsa_circ_198493,RMVar_hsa_circ_198494,RMVar_hsa_circ_340513,RMVar_hsa_circ_325095,RMVar_hsa_circ_198495,RMVar_hsa_circ_198496,RMVar_hsa_circ_51998,RMVar_hsa_circ_107836,RMVar_hsa_circ_115831,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_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_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_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_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_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_350684,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_198541,RMVar_hsa_circ_198538,RMVar_hsa_circ_198539,RMVar_hsa_circ_198537 18937 RMVar_ID_18937 Human_SNP_ID_66113868 A-to-I Human chr2 + 32519547 32519547 32519547 ATTTATTTATTTAATTTTGAGAGGGGGGTCTCACTCTGTCACCCAGGCTGAAGTGCAGTGGAACG ATTTATTTATTTAATTTTGAGAGGGGGGTCTCCCTCTGTCACCCAGGCTGAAGTGCAGTGGAACG A C BIRC6 Ensembl:ENSG00000115760 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1298037144 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_774286,Human_RBP_ID_8517721,Human_RBP_ID_13864603 RMVar_hsa_circ_316322,RMVar_hsa_circ_47783,RMVar_hsa_circ_25859,RMVar_hsa_circ_51154,RMVar_hsa_circ_362690,RMVar_hsa_circ_346186,RMVar_hsa_circ_307492,RMVar_hsa_circ_281035,RMVar_hsa_circ_75196,RMVar_hsa_circ_33306,RMVar_hsa_circ_65955,RMVar_hsa_circ_339840,RMVar_hsa_circ_41889,RMVar_hsa_circ_9084,RMVar_hsa_circ_66172,RMVar_hsa_circ_119839,RMVar_hsa_circ_99283,RMVar_hsa_circ_198489,RMVar_hsa_circ_54548,RMVar_hsa_circ_198494,RMVar_hsa_circ_107836,RMVar_hsa_circ_115831,RMVar_hsa_circ_269560,RMVar_hsa_circ_112318,RMVar_hsa_circ_111552,RMVar_hsa_circ_106383,RMVar_hsa_circ_6022,RMVar_hsa_circ_18585,RMVar_hsa_circ_107127,RMVar_hsa_circ_198504,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_323044,RMVar_hsa_circ_91605,RMVar_hsa_circ_198521,RMVar_hsa_circ_119573,RMVar_hsa_circ_198518,RMVar_hsa_circ_376028,RMVar_hsa_circ_358069,RMVar_hsa_circ_121516,RMVar_hsa_circ_120631,RMVar_hsa_circ_116965,RMVar_hsa_circ_198525,RMVar_hsa_circ_198526,RMVar_hsa_circ_198523,RMVar_hsa_circ_198524,RMVar_hsa_circ_198522,RMVar_hsa_circ_118753,RMVar_hsa_circ_107594,RMVar_hsa_circ_198536,RMVar_hsa_circ_350684,RMVar_hsa_circ_93776,RMVar_hsa_circ_97410,RMVar_hsa_circ_84343,RMVar_hsa_circ_47300,RMVar_hsa_circ_99073,RMVar_hsa_circ_198540,RMVar_hsa_circ_198541,RMVar_hsa_circ_198538,RMVar_hsa_circ_198539,RMVar_hsa_circ_366476,RMVar_hsa_circ_198537,RMVar_hsa_circ_360764,RMVar_hsa_circ_89951,RMVar_hsa_circ_68961,RMVar_hsa_circ_22316,RMVar_hsa_circ_281221,RMVar_hsa_circ_198547,RMVar_hsa_circ_198548,RMVar_hsa_circ_198549,RMVar_hsa_circ_319411,RMVar_hsa_circ_321516,RMVar_hsa_circ_331303,RMVar_hsa_circ_320187,RMVar_hsa_circ_300588,RMVar_hsa_circ_121336,RMVar_hsa_circ_72747,RMVar_hsa_circ_104784,RMVar_hsa_circ_198550,RMVar_hsa_circ_198554,RMVar_hsa_circ_12673,RMVar_hsa_circ_198555,RMVar_hsa_circ_198552,RMVar_hsa_circ_198553,RMVar_hsa_circ_198551,RMVar_hsa_circ_102276,RMVar_hsa_circ_330232,RMVar_hsa_circ_198558,RMVar_hsa_circ_103910,RMVar_hsa_circ_59642,RMVar_hsa_circ_22084,RMVar_hsa_circ_111473,RMVar_hsa_circ_198560,RMVar_hsa_circ_198561,RMVar_hsa_circ_198562,RMVar_hsa_circ_113519,RMVar_hsa_circ_304735,RMVar_hsa_circ_198564,RMVar_hsa_circ_88817,RMVar_hsa_circ_198565,RMVar_hsa_circ_332716,RMVar_hsa_circ_364936,RMVar_hsa_circ_198563,RMVar_hsa_circ_308714,RMVar_hsa_circ_96124,RMVar_hsa_circ_85669,RMVar_hsa_circ_198573,RMVar_hsa_circ_87738,RMVar_hsa_circ_198568,RMVar_hsa_circ_198570,RMVar_hsa_circ_198571,RMVar_hsa_circ_198572,RMVar_hsa_circ_198569,RMVar_hsa_circ_111691,RMVar_hsa_circ_89765,RMVar_hsa_circ_33651,RMVar_hsa_circ_35047,RMVar_hsa_circ_198574,RMVar_hsa_circ_198575,RMVar_hsa_circ_14934,RMVar_hsa_circ_95380,RMVar_hsa_circ_198576 18938 RMVar_ID_18938 Human_SNP_ID_66114164 A-to-I Human chr2 + 32520706 32520706 32520706 GGGTATGATAGCGTGCACCTGTAGTCCCACCTATCTGGGGGACTGAGGTAGGAAAATCACTTGAA GGGTATGATAGCGTGCACCTGTAGTCCCACCTCTCTGGGGGACTGAGGTAGGAAAATCACTTGAA A C BIRC6 Ensembl:ENSG00000115760 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs547262982 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569511 RMVar_hsa_circ_316322,RMVar_hsa_circ_47783,RMVar_hsa_circ_25859,RMVar_hsa_circ_51154,RMVar_hsa_circ_362690,RMVar_hsa_circ_346186,RMVar_hsa_circ_307492,RMVar_hsa_circ_281035,RMVar_hsa_circ_75196,RMVar_hsa_circ_33306,RMVar_hsa_circ_65955,RMVar_hsa_circ_339840,RMVar_hsa_circ_41889,RMVar_hsa_circ_9084,RMVar_hsa_circ_66172,RMVar_hsa_circ_119839,RMVar_hsa_circ_99283,RMVar_hsa_circ_198489,RMVar_hsa_circ_54548,RMVar_hsa_circ_198494,RMVar_hsa_circ_107836,RMVar_hsa_circ_115831,RMVar_hsa_circ_269560,RMVar_hsa_circ_112318,RMVar_hsa_circ_111552,RMVar_hsa_circ_106383,RMVar_hsa_circ_6022,RMVar_hsa_circ_18585,RMVar_hsa_circ_107127,RMVar_hsa_circ_198504,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_323044,RMVar_hsa_circ_91605,RMVar_hsa_circ_198521,RMVar_hsa_circ_119573,RMVar_hsa_circ_198518,RMVar_hsa_circ_376028,RMVar_hsa_circ_358069,RMVar_hsa_circ_121516,RMVar_hsa_circ_120631,RMVar_hsa_circ_116965,RMVar_hsa_circ_198525,RMVar_hsa_circ_198526,RMVar_hsa_circ_198523,RMVar_hsa_circ_198524,RMVar_hsa_circ_198522,RMVar_hsa_circ_118753,RMVar_hsa_circ_107594,RMVar_hsa_circ_198536,RMVar_hsa_circ_350684,RMVar_hsa_circ_93776,RMVar_hsa_circ_97410,RMVar_hsa_circ_84343,RMVar_hsa_circ_47300,RMVar_hsa_circ_99073,RMVar_hsa_circ_198540,RMVar_hsa_circ_198541,RMVar_hsa_circ_198538,RMVar_hsa_circ_198539,RMVar_hsa_circ_366476,RMVar_hsa_circ_198537,RMVar_hsa_circ_360764,RMVar_hsa_circ_89951,RMVar_hsa_circ_68961,RMVar_hsa_circ_22316,RMVar_hsa_circ_281221,RMVar_hsa_circ_198547,RMVar_hsa_circ_198548,RMVar_hsa_circ_198549,RMVar_hsa_circ_319411,RMVar_hsa_circ_321516,RMVar_hsa_circ_331303,RMVar_hsa_circ_320187,RMVar_hsa_circ_300588,RMVar_hsa_circ_121336,RMVar_hsa_circ_72747,RMVar_hsa_circ_104784,RMVar_hsa_circ_198550,RMVar_hsa_circ_198554,RMVar_hsa_circ_12673,RMVar_hsa_circ_198555,RMVar_hsa_circ_198552,RMVar_hsa_circ_198553,RMVar_hsa_circ_198551,RMVar_hsa_circ_102276,RMVar_hsa_circ_330232,RMVar_hsa_circ_198558,RMVar_hsa_circ_103910,RMVar_hsa_circ_59642,RMVar_hsa_circ_22084,RMVar_hsa_circ_111473,RMVar_hsa_circ_198560,RMVar_hsa_circ_198561,RMVar_hsa_circ_198562,RMVar_hsa_circ_113519,RMVar_hsa_circ_304735,RMVar_hsa_circ_198564,RMVar_hsa_circ_88817,RMVar_hsa_circ_198565,RMVar_hsa_circ_332716,RMVar_hsa_circ_364936,RMVar_hsa_circ_198563,RMVar_hsa_circ_308714,RMVar_hsa_circ_96124,RMVar_hsa_circ_85669,RMVar_hsa_circ_198573,RMVar_hsa_circ_87738,RMVar_hsa_circ_198568,RMVar_hsa_circ_198570,RMVar_hsa_circ_198571,RMVar_hsa_circ_198572,RMVar_hsa_circ_198569,RMVar_hsa_circ_111691,RMVar_hsa_circ_89765,RMVar_hsa_circ_33651,RMVar_hsa_circ_35047,RMVar_hsa_circ_198574,RMVar_hsa_circ_198575,RMVar_hsa_circ_14934,RMVar_hsa_circ_95380,RMVar_hsa_circ_198576 18939 RMVar_ID_18939 Human_SNP_ID_66114165 A-to-I Human chr2 + 32520706 32520706 32520706 GGGTATGATAGCGTGCACCTGTAGTCCCACCTATCTGGGGGACTGAGGTAGGAAAATCACTTGAA GGGTATGATAGCGTGCACCTGTAGTCCCACCTGTCTGGGGGACTGAGGTAGGAAAATCACTTGAA A G BIRC6 Ensembl:ENSG00000115760 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs547262982 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569511 RMVar_hsa_circ_316322,RMVar_hsa_circ_47783,RMVar_hsa_circ_25859,RMVar_hsa_circ_51154,RMVar_hsa_circ_362690,RMVar_hsa_circ_346186,RMVar_hsa_circ_307492,RMVar_hsa_circ_281035,RMVar_hsa_circ_75196,RMVar_hsa_circ_33306,RMVar_hsa_circ_65955,RMVar_hsa_circ_339840,RMVar_hsa_circ_41889,RMVar_hsa_circ_9084,RMVar_hsa_circ_66172,RMVar_hsa_circ_119839,RMVar_hsa_circ_99283,RMVar_hsa_circ_198489,RMVar_hsa_circ_54548,RMVar_hsa_circ_198494,RMVar_hsa_circ_107836,RMVar_hsa_circ_115831,RMVar_hsa_circ_269560,RMVar_hsa_circ_112318,RMVar_hsa_circ_111552,RMVar_hsa_circ_106383,RMVar_hsa_circ_6022,RMVar_hsa_circ_18585,RMVar_hsa_circ_107127,RMVar_hsa_circ_198504,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_323044,RMVar_hsa_circ_91605,RMVar_hsa_circ_198521,RMVar_hsa_circ_119573,RMVar_hsa_circ_198518,RMVar_hsa_circ_376028,RMVar_hsa_circ_358069,RMVar_hsa_circ_121516,RMVar_hsa_circ_120631,RMVar_hsa_circ_116965,RMVar_hsa_circ_198525,RMVar_hsa_circ_198526,RMVar_hsa_circ_198523,RMVar_hsa_circ_198524,RMVar_hsa_circ_198522,RMVar_hsa_circ_118753,RMVar_hsa_circ_107594,RMVar_hsa_circ_198536,RMVar_hsa_circ_350684,RMVar_hsa_circ_93776,RMVar_hsa_circ_97410,RMVar_hsa_circ_84343,RMVar_hsa_circ_47300,RMVar_hsa_circ_99073,RMVar_hsa_circ_198540,RMVar_hsa_circ_198541,RMVar_hsa_circ_198538,RMVar_hsa_circ_198539,RMVar_hsa_circ_366476,RMVar_hsa_circ_198537,RMVar_hsa_circ_360764,RMVar_hsa_circ_89951,RMVar_hsa_circ_68961,RMVar_hsa_circ_22316,RMVar_hsa_circ_281221,RMVar_hsa_circ_198547,RMVar_hsa_circ_198548,RMVar_hsa_circ_198549,RMVar_hsa_circ_319411,RMVar_hsa_circ_321516,RMVar_hsa_circ_331303,RMVar_hsa_circ_320187,RMVar_hsa_circ_300588,RMVar_hsa_circ_121336,RMVar_hsa_circ_72747,RMVar_hsa_circ_104784,RMVar_hsa_circ_198550,RMVar_hsa_circ_198554,RMVar_hsa_circ_12673,RMVar_hsa_circ_198555,RMVar_hsa_circ_198552,RMVar_hsa_circ_198553,RMVar_hsa_circ_198551,RMVar_hsa_circ_102276,RMVar_hsa_circ_330232,RMVar_hsa_circ_198558,RMVar_hsa_circ_103910,RMVar_hsa_circ_59642,RMVar_hsa_circ_22084,RMVar_hsa_circ_111473,RMVar_hsa_circ_198560,RMVar_hsa_circ_198561,RMVar_hsa_circ_198562,RMVar_hsa_circ_113519,RMVar_hsa_circ_304735,RMVar_hsa_circ_198564,RMVar_hsa_circ_88817,RMVar_hsa_circ_198565,RMVar_hsa_circ_332716,RMVar_hsa_circ_364936,RMVar_hsa_circ_198563,RMVar_hsa_circ_308714,RMVar_hsa_circ_96124,RMVar_hsa_circ_85669,RMVar_hsa_circ_198573,RMVar_hsa_circ_87738,RMVar_hsa_circ_198568,RMVar_hsa_circ_198570,RMVar_hsa_circ_198571,RMVar_hsa_circ_198572,RMVar_hsa_circ_198569,RMVar_hsa_circ_111691,RMVar_hsa_circ_89765,RMVar_hsa_circ_33651,RMVar_hsa_circ_35047,RMVar_hsa_circ_198574,RMVar_hsa_circ_198575,RMVar_hsa_circ_14934,RMVar_hsa_circ_95380,RMVar_hsa_circ_198576 18940 RMVar_ID_18940 Human_SNP_ID_66114172 A-to-I Human chr2 + 32520732 32520732 32520732 CCACCTATCTGGGGGACTGAGGTAGGAAAATCACTTGAACCCTAGAGGTGGAGGTTACGGTGAGC CCACCTATCTGGGGGACTGAGGTAGGAAAATCCCTTGAACCCTAGAGGTGGAGGTTACGGTGAGC A C BIRC6 Ensembl:ENSG00000115760 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs910375268 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569511 RMVar_hsa_circ_316322,RMVar_hsa_circ_47783,RMVar_hsa_circ_25859,RMVar_hsa_circ_51154,RMVar_hsa_circ_362690,RMVar_hsa_circ_346186,RMVar_hsa_circ_307492,RMVar_hsa_circ_281035,RMVar_hsa_circ_75196,RMVar_hsa_circ_33306,RMVar_hsa_circ_65955,RMVar_hsa_circ_339840,RMVar_hsa_circ_41889,RMVar_hsa_circ_9084,RMVar_hsa_circ_66172,RMVar_hsa_circ_119839,RMVar_hsa_circ_99283,RMVar_hsa_circ_198489,RMVar_hsa_circ_54548,RMVar_hsa_circ_198494,RMVar_hsa_circ_107836,RMVar_hsa_circ_115831,RMVar_hsa_circ_269560,RMVar_hsa_circ_112318,RMVar_hsa_circ_111552,RMVar_hsa_circ_106383,RMVar_hsa_circ_6022,RMVar_hsa_circ_18585,RMVar_hsa_circ_107127,RMVar_hsa_circ_198504,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_323044,RMVar_hsa_circ_91605,RMVar_hsa_circ_198521,RMVar_hsa_circ_119573,RMVar_hsa_circ_198518,RMVar_hsa_circ_376028,RMVar_hsa_circ_358069,RMVar_hsa_circ_121516,RMVar_hsa_circ_120631,RMVar_hsa_circ_116965,RMVar_hsa_circ_198525,RMVar_hsa_circ_198526,RMVar_hsa_circ_198523,RMVar_hsa_circ_198524,RMVar_hsa_circ_198522,RMVar_hsa_circ_118753,RMVar_hsa_circ_107594,RMVar_hsa_circ_198536,RMVar_hsa_circ_350684,RMVar_hsa_circ_93776,RMVar_hsa_circ_97410,RMVar_hsa_circ_84343,RMVar_hsa_circ_47300,RMVar_hsa_circ_99073,RMVar_hsa_circ_198540,RMVar_hsa_circ_198541,RMVar_hsa_circ_198538,RMVar_hsa_circ_198539,RMVar_hsa_circ_366476,RMVar_hsa_circ_198537,RMVar_hsa_circ_360764,RMVar_hsa_circ_89951,RMVar_hsa_circ_68961,RMVar_hsa_circ_22316,RMVar_hsa_circ_281221,RMVar_hsa_circ_198547,RMVar_hsa_circ_198548,RMVar_hsa_circ_198549,RMVar_hsa_circ_319411,RMVar_hsa_circ_321516,RMVar_hsa_circ_331303,RMVar_hsa_circ_320187,RMVar_hsa_circ_300588,RMVar_hsa_circ_121336,RMVar_hsa_circ_72747,RMVar_hsa_circ_104784,RMVar_hsa_circ_198550,RMVar_hsa_circ_198554,RMVar_hsa_circ_12673,RMVar_hsa_circ_198555,RMVar_hsa_circ_198552,RMVar_hsa_circ_198553,RMVar_hsa_circ_198551,RMVar_hsa_circ_102276,RMVar_hsa_circ_330232,RMVar_hsa_circ_198558,RMVar_hsa_circ_103910,RMVar_hsa_circ_59642,RMVar_hsa_circ_22084,RMVar_hsa_circ_111473,RMVar_hsa_circ_198560,RMVar_hsa_circ_198561,RMVar_hsa_circ_198562,RMVar_hsa_circ_113519,RMVar_hsa_circ_304735,RMVar_hsa_circ_198564,RMVar_hsa_circ_88817,RMVar_hsa_circ_198565,RMVar_hsa_circ_332716,RMVar_hsa_circ_364936,RMVar_hsa_circ_198563,RMVar_hsa_circ_308714,RMVar_hsa_circ_96124,RMVar_hsa_circ_85669,RMVar_hsa_circ_198573,RMVar_hsa_circ_87738,RMVar_hsa_circ_198568,RMVar_hsa_circ_198570,RMVar_hsa_circ_198571,RMVar_hsa_circ_198572,RMVar_hsa_circ_198569,RMVar_hsa_circ_111691,RMVar_hsa_circ_89765,RMVar_hsa_circ_33651,RMVar_hsa_circ_35047,RMVar_hsa_circ_198574,RMVar_hsa_circ_198575,RMVar_hsa_circ_14934,RMVar_hsa_circ_95380,RMVar_hsa_circ_198576 18941 RMVar_ID_18941 Human_SNP_ID_66114434 A-to-I Human chr2 + 32521503 32521503 32521503 GTTTTTTGTTTTTTGTTTTGAGACGGAGTCTCACTCTGTCCCCCAGGCTGTGCAGTGGCGCGATC GTTTTTTGTTTTTTGTTTTGAGACGGAGTCTCGCTCTGTCCCCCAGGCTGTGCAGTGGCGCGATC A G BIRC6 Ensembl:ENSG00000115760 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs936246454 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14000818 RMVar_hsa_circ_316322,RMVar_hsa_circ_47783,RMVar_hsa_circ_25859,RMVar_hsa_circ_51154,RMVar_hsa_circ_362690,RMVar_hsa_circ_346186,RMVar_hsa_circ_307492,RMVar_hsa_circ_281035,RMVar_hsa_circ_75196,RMVar_hsa_circ_33306,RMVar_hsa_circ_65955,RMVar_hsa_circ_339840,RMVar_hsa_circ_41889,RMVar_hsa_circ_9084,RMVar_hsa_circ_66172,RMVar_hsa_circ_119839,RMVar_hsa_circ_99283,RMVar_hsa_circ_198489,RMVar_hsa_circ_54548,RMVar_hsa_circ_198494,RMVar_hsa_circ_107836,RMVar_hsa_circ_115831,RMVar_hsa_circ_269560,RMVar_hsa_circ_112318,RMVar_hsa_circ_111552,RMVar_hsa_circ_106383,RMVar_hsa_circ_6022,RMVar_hsa_circ_18585,RMVar_hsa_circ_107127,RMVar_hsa_circ_198504,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_323044,RMVar_hsa_circ_91605,RMVar_hsa_circ_198521,RMVar_hsa_circ_119573,RMVar_hsa_circ_198518,RMVar_hsa_circ_376028,RMVar_hsa_circ_358069,RMVar_hsa_circ_121516,RMVar_hsa_circ_120631,RMVar_hsa_circ_116965,RMVar_hsa_circ_198525,RMVar_hsa_circ_198526,RMVar_hsa_circ_198523,RMVar_hsa_circ_198524,RMVar_hsa_circ_198522,RMVar_hsa_circ_118753,RMVar_hsa_circ_107594,RMVar_hsa_circ_198536,RMVar_hsa_circ_350684,RMVar_hsa_circ_93776,RMVar_hsa_circ_97410,RMVar_hsa_circ_84343,RMVar_hsa_circ_47300,RMVar_hsa_circ_99073,RMVar_hsa_circ_198540,RMVar_hsa_circ_198541,RMVar_hsa_circ_198538,RMVar_hsa_circ_198539,RMVar_hsa_circ_366476,RMVar_hsa_circ_198537,RMVar_hsa_circ_360764,RMVar_hsa_circ_89951,RMVar_hsa_circ_68961,RMVar_hsa_circ_22316,RMVar_hsa_circ_281221,RMVar_hsa_circ_198547,RMVar_hsa_circ_198548,RMVar_hsa_circ_198549,RMVar_hsa_circ_319411,RMVar_hsa_circ_321516,RMVar_hsa_circ_331303,RMVar_hsa_circ_320187,RMVar_hsa_circ_300588,RMVar_hsa_circ_121336,RMVar_hsa_circ_72747,RMVar_hsa_circ_104784,RMVar_hsa_circ_198550,RMVar_hsa_circ_198554,RMVar_hsa_circ_12673,RMVar_hsa_circ_198555,RMVar_hsa_circ_198552,RMVar_hsa_circ_198553,RMVar_hsa_circ_198551,RMVar_hsa_circ_102276,RMVar_hsa_circ_330232,RMVar_hsa_circ_198558,RMVar_hsa_circ_103910,RMVar_hsa_circ_59642,RMVar_hsa_circ_22084,RMVar_hsa_circ_111473,RMVar_hsa_circ_198560,RMVar_hsa_circ_198561,RMVar_hsa_circ_198562,RMVar_hsa_circ_113519,RMVar_hsa_circ_304735,RMVar_hsa_circ_198564,RMVar_hsa_circ_88817,RMVar_hsa_circ_198565,RMVar_hsa_circ_332716,RMVar_hsa_circ_364936,RMVar_hsa_circ_198563,RMVar_hsa_circ_308714,RMVar_hsa_circ_96124,RMVar_hsa_circ_85669,RMVar_hsa_circ_198573,RMVar_hsa_circ_87738,RMVar_hsa_circ_198568,RMVar_hsa_circ_198570,RMVar_hsa_circ_198571,RMVar_hsa_circ_198572,RMVar_hsa_circ_198569,RMVar_hsa_circ_111691,RMVar_hsa_circ_89765,RMVar_hsa_circ_33651,RMVar_hsa_circ_35047,RMVar_hsa_circ_198574,RMVar_hsa_circ_198575,RMVar_hsa_circ_14934,RMVar_hsa_circ_95380,RMVar_hsa_circ_198576 18942 RMVar_ID_18942 Human_SNP_ID_66114435 A-to-I Human chr2 + 32521503 32521503 32521503 GTTTTTTGTTTTTTGTTTTGAGACGGAGTCTCACTCTGTCCCCCAGGCTGTGCAGTGGCGCGATC GTTTTTTGTTTTTTGTTTTGAGACGGAGTCTCTCTCTGTCCCCCAGGCTGTGCAGTGGCGCGATC A T BIRC6 Ensembl:ENSG00000115760 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs936246454 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14000818 RMVar_hsa_circ_316322,RMVar_hsa_circ_47783,RMVar_hsa_circ_25859,RMVar_hsa_circ_51154,RMVar_hsa_circ_362690,RMVar_hsa_circ_346186,RMVar_hsa_circ_307492,RMVar_hsa_circ_281035,RMVar_hsa_circ_75196,RMVar_hsa_circ_33306,RMVar_hsa_circ_65955,RMVar_hsa_circ_339840,RMVar_hsa_circ_41889,RMVar_hsa_circ_9084,RMVar_hsa_circ_66172,RMVar_hsa_circ_119839,RMVar_hsa_circ_99283,RMVar_hsa_circ_198489,RMVar_hsa_circ_54548,RMVar_hsa_circ_198494,RMVar_hsa_circ_107836,RMVar_hsa_circ_115831,RMVar_hsa_circ_269560,RMVar_hsa_circ_112318,RMVar_hsa_circ_111552,RMVar_hsa_circ_106383,RMVar_hsa_circ_6022,RMVar_hsa_circ_18585,RMVar_hsa_circ_107127,RMVar_hsa_circ_198504,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_323044,RMVar_hsa_circ_91605,RMVar_hsa_circ_198521,RMVar_hsa_circ_119573,RMVar_hsa_circ_198518,RMVar_hsa_circ_376028,RMVar_hsa_circ_358069,RMVar_hsa_circ_121516,RMVar_hsa_circ_120631,RMVar_hsa_circ_116965,RMVar_hsa_circ_198525,RMVar_hsa_circ_198526,RMVar_hsa_circ_198523,RMVar_hsa_circ_198524,RMVar_hsa_circ_198522,RMVar_hsa_circ_118753,RMVar_hsa_circ_107594,RMVar_hsa_circ_198536,RMVar_hsa_circ_350684,RMVar_hsa_circ_93776,RMVar_hsa_circ_97410,RMVar_hsa_circ_84343,RMVar_hsa_circ_47300,RMVar_hsa_circ_99073,RMVar_hsa_circ_198540,RMVar_hsa_circ_198541,RMVar_hsa_circ_198538,RMVar_hsa_circ_198539,RMVar_hsa_circ_366476,RMVar_hsa_circ_198537,RMVar_hsa_circ_360764,RMVar_hsa_circ_89951,RMVar_hsa_circ_68961,RMVar_hsa_circ_22316,RMVar_hsa_circ_281221,RMVar_hsa_circ_198547,RMVar_hsa_circ_198548,RMVar_hsa_circ_198549,RMVar_hsa_circ_319411,RMVar_hsa_circ_321516,RMVar_hsa_circ_331303,RMVar_hsa_circ_320187,RMVar_hsa_circ_300588,RMVar_hsa_circ_121336,RMVar_hsa_circ_72747,RMVar_hsa_circ_104784,RMVar_hsa_circ_198550,RMVar_hsa_circ_198554,RMVar_hsa_circ_12673,RMVar_hsa_circ_198555,RMVar_hsa_circ_198552,RMVar_hsa_circ_198553,RMVar_hsa_circ_198551,RMVar_hsa_circ_102276,RMVar_hsa_circ_330232,RMVar_hsa_circ_198558,RMVar_hsa_circ_103910,RMVar_hsa_circ_59642,RMVar_hsa_circ_22084,RMVar_hsa_circ_111473,RMVar_hsa_circ_198560,RMVar_hsa_circ_198561,RMVar_hsa_circ_198562,RMVar_hsa_circ_113519,RMVar_hsa_circ_304735,RMVar_hsa_circ_198564,RMVar_hsa_circ_88817,RMVar_hsa_circ_198565,RMVar_hsa_circ_332716,RMVar_hsa_circ_364936,RMVar_hsa_circ_198563,RMVar_hsa_circ_308714,RMVar_hsa_circ_96124,RMVar_hsa_circ_85669,RMVar_hsa_circ_198573,RMVar_hsa_circ_87738,RMVar_hsa_circ_198568,RMVar_hsa_circ_198570,RMVar_hsa_circ_198571,RMVar_hsa_circ_198572,RMVar_hsa_circ_198569,RMVar_hsa_circ_111691,RMVar_hsa_circ_89765,RMVar_hsa_circ_33651,RMVar_hsa_circ_35047,RMVar_hsa_circ_198574,RMVar_hsa_circ_198575,RMVar_hsa_circ_14934,RMVar_hsa_circ_95380,RMVar_hsa_circ_198576 18943 RMVar_ID_18943 Human_SNP_ID_66114497 A-to-I Human chr2 + 32521682 32521682 32521682 TTTTTTTTTTAGTAGAGATGGGGTTTTGTCATATTGGCCATGCTGATGTCGAACTCCTGACCTCA TTTTTTTTTTAGTAGAGATGGGGTTTTGTCATTTTGGCCATGCTGATGTCGAACTCCTGACCTCA A T BIRC6 Ensembl:ENSG00000115760 Protein coding intron GSE38233;GSE107867 cultured B-cells;ASD brains,frontal_cortex - 24183664,30559470 RNA-Seq:(High) rs1401223837 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13864652,Human_RBP_ID_25536089 RMVar_hsa_circ_316322,RMVar_hsa_circ_47783,RMVar_hsa_circ_25859,RMVar_hsa_circ_51154,RMVar_hsa_circ_362690,RMVar_hsa_circ_346186,RMVar_hsa_circ_307492,RMVar_hsa_circ_281035,RMVar_hsa_circ_75196,RMVar_hsa_circ_33306,RMVar_hsa_circ_65955,RMVar_hsa_circ_339840,RMVar_hsa_circ_41889,RMVar_hsa_circ_9084,RMVar_hsa_circ_66172,RMVar_hsa_circ_119839,RMVar_hsa_circ_99283,RMVar_hsa_circ_198489,RMVar_hsa_circ_54548,RMVar_hsa_circ_198494,RMVar_hsa_circ_107836,RMVar_hsa_circ_115831,RMVar_hsa_circ_269560,RMVar_hsa_circ_112318,RMVar_hsa_circ_111552,RMVar_hsa_circ_106383,RMVar_hsa_circ_6022,RMVar_hsa_circ_18585,RMVar_hsa_circ_107127,RMVar_hsa_circ_198504,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_323044,RMVar_hsa_circ_91605,RMVar_hsa_circ_198521,RMVar_hsa_circ_119573,RMVar_hsa_circ_198518,RMVar_hsa_circ_376028,RMVar_hsa_circ_358069,RMVar_hsa_circ_121516,RMVar_hsa_circ_120631,RMVar_hsa_circ_116965,RMVar_hsa_circ_198525,RMVar_hsa_circ_198526,RMVar_hsa_circ_198523,RMVar_hsa_circ_198524,RMVar_hsa_circ_198522,RMVar_hsa_circ_118753,RMVar_hsa_circ_107594,RMVar_hsa_circ_198536,RMVar_hsa_circ_350684,RMVar_hsa_circ_93776,RMVar_hsa_circ_97410,RMVar_hsa_circ_84343,RMVar_hsa_circ_47300,RMVar_hsa_circ_99073,RMVar_hsa_circ_198540,RMVar_hsa_circ_198541,RMVar_hsa_circ_198538,RMVar_hsa_circ_198539,RMVar_hsa_circ_366476,RMVar_hsa_circ_198537,RMVar_hsa_circ_360764,RMVar_hsa_circ_89951,RMVar_hsa_circ_68961,RMVar_hsa_circ_22316,RMVar_hsa_circ_281221,RMVar_hsa_circ_198547,RMVar_hsa_circ_198548,RMVar_hsa_circ_198549,RMVar_hsa_circ_319411,RMVar_hsa_circ_321516,RMVar_hsa_circ_331303,RMVar_hsa_circ_320187,RMVar_hsa_circ_300588,RMVar_hsa_circ_121336,RMVar_hsa_circ_72747,RMVar_hsa_circ_104784,RMVar_hsa_circ_198550,RMVar_hsa_circ_198554,RMVar_hsa_circ_12673,RMVar_hsa_circ_198555,RMVar_hsa_circ_198552,RMVar_hsa_circ_198553,RMVar_hsa_circ_198551,RMVar_hsa_circ_102276,RMVar_hsa_circ_330232,RMVar_hsa_circ_198558,RMVar_hsa_circ_103910,RMVar_hsa_circ_59642,RMVar_hsa_circ_22084,RMVar_hsa_circ_111473,RMVar_hsa_circ_198560,RMVar_hsa_circ_198561,RMVar_hsa_circ_198562,RMVar_hsa_circ_113519,RMVar_hsa_circ_304735,RMVar_hsa_circ_198564,RMVar_hsa_circ_88817,RMVar_hsa_circ_198565,RMVar_hsa_circ_332716,RMVar_hsa_circ_364936,RMVar_hsa_circ_198563,RMVar_hsa_circ_308714,RMVar_hsa_circ_96124,RMVar_hsa_circ_85669,RMVar_hsa_circ_198573,RMVar_hsa_circ_87738,RMVar_hsa_circ_198568,RMVar_hsa_circ_198570,RMVar_hsa_circ_198571,RMVar_hsa_circ_198572,RMVar_hsa_circ_198569,RMVar_hsa_circ_111691,RMVar_hsa_circ_89765,RMVar_hsa_circ_33651,RMVar_hsa_circ_35047,RMVar_hsa_circ_198574,RMVar_hsa_circ_198575,RMVar_hsa_circ_14934,RMVar_hsa_circ_95380,RMVar_hsa_circ_198576 18944 RMVar_ID_18944 Human_SNP_ID_66129378 A-to-I Human chr2 + 32574253 32574253 32574253 GCATGATCTTGTCCTCCCCAGTTGCAGGGACTACAGGTGTGCGCCACCACGCCCAGCTAATTTTT GCATGATCTTGTCCTCCCCAGTTGCAGGGACTGCAGGTGTGCGCCACCACGCCCAGCTAATTTTT A G BIRC6 Ensembl:ENSG00000115760 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs908953592 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51154,RMVar_hsa_circ_346186,RMVar_hsa_circ_7021,RMVar_hsa_circ_75196,RMVar_hsa_circ_65955,RMVar_hsa_circ_119839,RMVar_hsa_circ_99283,RMVar_hsa_circ_198489,RMVar_hsa_circ_198494,RMVar_hsa_circ_107836,RMVar_hsa_circ_111552,RMVar_hsa_circ_18585,RMVar_hsa_circ_107127,RMVar_hsa_circ_198502,RMVar_hsa_circ_198501,RMVar_hsa_circ_198516,RMVar_hsa_circ_79240,RMVar_hsa_circ_198517,RMVar_hsa_circ_323044,RMVar_hsa_circ_91605,RMVar_hsa_circ_198521,RMVar_hsa_circ_119573,RMVar_hsa_circ_198518,RMVar_hsa_circ_376028,RMVar_hsa_circ_121516,RMVar_hsa_circ_198523,RMVar_hsa_circ_198522,RMVar_hsa_circ_107594,RMVar_hsa_circ_198536,RMVar_hsa_circ_93776,RMVar_hsa_circ_84343,RMVar_hsa_circ_47300,RMVar_hsa_circ_99073,RMVar_hsa_circ_198538,RMVar_hsa_circ_198537,RMVar_hsa_circ_360764,RMVar_hsa_circ_89951,RMVar_hsa_circ_68961,RMVar_hsa_circ_281221,RMVar_hsa_circ_198548,RMVar_hsa_circ_198549,RMVar_hsa_circ_319411,RMVar_hsa_circ_320187,RMVar_hsa_circ_300588,RMVar_hsa_circ_72747,RMVar_hsa_circ_198550,RMVar_hsa_circ_12673,RMVar_hsa_circ_198551,RMVar_hsa_circ_102276,RMVar_hsa_circ_330232,RMVar_hsa_circ_198558,RMVar_hsa_circ_103910,RMVar_hsa_circ_59642,RMVar_hsa_circ_15468,RMVar_hsa_circ_22084,RMVar_hsa_circ_198560,RMVar_hsa_circ_198561,RMVar_hsa_circ_198562,RMVar_hsa_circ_88817,RMVar_hsa_circ_364936,RMVar_hsa_circ_198563,RMVar_hsa_circ_87738,RMVar_hsa_circ_198572,RMVar_hsa_circ_111691,RMVar_hsa_circ_33651,RMVar_hsa_circ_198574,RMVar_hsa_circ_198575,RMVar_hsa_circ_300851,RMVar_hsa_circ_95380,RMVar_hsa_circ_198576,RMVar_hsa_circ_323671,RMVar_hsa_circ_330542,RMVar_hsa_circ_301453,RMVar_hsa_circ_274775,RMVar_hsa_circ_66885,RMVar_hsa_circ_18567,RMVar_hsa_circ_198579,RMVar_hsa_circ_198580,RMVar_hsa_circ_198581,RMVar_hsa_circ_93667,RMVar_hsa_circ_298873,RMVar_hsa_circ_322879,RMVar_hsa_circ_198582,RMVar_hsa_circ_98502,RMVar_hsa_circ_198585,RMVar_hsa_circ_198586,RMVar_hsa_circ_373766,RMVar_hsa_circ_198587,RMVar_hsa_circ_304588,RMVar_hsa_circ_100039,RMVar_hsa_circ_293189,RMVar_hsa_circ_38504,RMVar_hsa_circ_101736,RMVar_hsa_circ_198592,RMVar_hsa_circ_198593,RMVar_hsa_circ_198594,RMVar_hsa_circ_198591,RMVar_hsa_circ_94460,RMVar_hsa_circ_198595,RMVar_hsa_circ_111441,RMVar_hsa_circ_198596,RMVar_hsa_circ_198597,RMVar_hsa_circ_198598,RMVar_hsa_circ_356397 18945 RMVar_ID_18945 Human_SNP_ID_66131840 A-to-I Human chr2 + 32582667 32582667 32582667 CGCACCCGTAATCCCAGCTACCGAGGCAGGAGAATCACTTGAACCCAGGAGGCAGAGGTTGCGGT CGCACCCGTAATCCCAGCTACCGAGGCAGGAGGATCACTTGAACCCAGGAGGCAGAGGTTGCGGT A G BIRC6 Ensembl:ENSG00000115760 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1032539420 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51154,RMVar_hsa_circ_7021,RMVar_hsa_circ_75196,RMVar_hsa_circ_65955,RMVar_hsa_circ_99283,RMVar_hsa_circ_198494,RMVar_hsa_circ_111552,RMVar_hsa_circ_18585,RMVar_hsa_circ_198501,RMVar_hsa_circ_79240,RMVar_hsa_circ_198517,RMVar_hsa_circ_91605,RMVar_hsa_circ_198521,RMVar_hsa_circ_119573,RMVar_hsa_circ_198518,RMVar_hsa_circ_376028,RMVar_hsa_circ_121516,RMVar_hsa_circ_198523,RMVar_hsa_circ_198522,RMVar_hsa_circ_107594,RMVar_hsa_circ_198536,RMVar_hsa_circ_93776,RMVar_hsa_circ_84343,RMVar_hsa_circ_47300,RMVar_hsa_circ_99073,RMVar_hsa_circ_198538,RMVar_hsa_circ_198537,RMVar_hsa_circ_89951,RMVar_hsa_circ_68961,RMVar_hsa_circ_198548,RMVar_hsa_circ_198549,RMVar_hsa_circ_319411,RMVar_hsa_circ_320187,RMVar_hsa_circ_300588,RMVar_hsa_circ_72747,RMVar_hsa_circ_198550,RMVar_hsa_circ_12673,RMVar_hsa_circ_102276,RMVar_hsa_circ_330232,RMVar_hsa_circ_198558,RMVar_hsa_circ_103910,RMVar_hsa_circ_15468,RMVar_hsa_circ_22084,RMVar_hsa_circ_198560,RMVar_hsa_circ_198561,RMVar_hsa_circ_198562,RMVar_hsa_circ_88817,RMVar_hsa_circ_198563,RMVar_hsa_circ_87738,RMVar_hsa_circ_111691,RMVar_hsa_circ_198574,RMVar_hsa_circ_198575,RMVar_hsa_circ_300851,RMVar_hsa_circ_95380,RMVar_hsa_circ_198576,RMVar_hsa_circ_323671,RMVar_hsa_circ_330542,RMVar_hsa_circ_301453,RMVar_hsa_circ_66885,RMVar_hsa_circ_18567,RMVar_hsa_circ_198579,RMVar_hsa_circ_198580,RMVar_hsa_circ_198581,RMVar_hsa_circ_322879,RMVar_hsa_circ_98502,RMVar_hsa_circ_198586,RMVar_hsa_circ_304588,RMVar_hsa_circ_100039,RMVar_hsa_circ_38504,RMVar_hsa_circ_332667,RMVar_hsa_circ_101736,RMVar_hsa_circ_198592,RMVar_hsa_circ_198593,RMVar_hsa_circ_198594,RMVar_hsa_circ_94460,RMVar_hsa_circ_198595,RMVar_hsa_circ_111441,RMVar_hsa_circ_198596,RMVar_hsa_circ_198597,RMVar_hsa_circ_343827,RMVar_hsa_circ_351421,RMVar_hsa_circ_341055,RMVar_hsa_circ_52799,RMVar_hsa_circ_305393,RMVar_hsa_circ_275356,RMVar_hsa_circ_198599,RMVar_hsa_circ_198600 18946 RMVar_ID_18946 Human_SNP_ID_66131842 A-to-I Human chr2 + 32582671 32582671 32582671 CCCGTAATCCCAGCTACCGAGGCAGGAGAATCACTTGAACCCAGGAGGCAGAGGTTGCGGTGAGC CCCGTAATCCCAGCTACCGAGGCAGGAGAATCGCTTGAACCCAGGAGGCAGAGGTTGCGGTGAGC A G BIRC6 Ensembl:ENSG00000115760 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs958215018 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51154,RMVar_hsa_circ_7021,RMVar_hsa_circ_75196,RMVar_hsa_circ_65955,RMVar_hsa_circ_99283,RMVar_hsa_circ_198494,RMVar_hsa_circ_111552,RMVar_hsa_circ_18585,RMVar_hsa_circ_198501,RMVar_hsa_circ_79240,RMVar_hsa_circ_198517,RMVar_hsa_circ_91605,RMVar_hsa_circ_198521,RMVar_hsa_circ_119573,RMVar_hsa_circ_198518,RMVar_hsa_circ_376028,RMVar_hsa_circ_121516,RMVar_hsa_circ_198523,RMVar_hsa_circ_198522,RMVar_hsa_circ_107594,RMVar_hsa_circ_198536,RMVar_hsa_circ_93776,RMVar_hsa_circ_84343,RMVar_hsa_circ_47300,RMVar_hsa_circ_99073,RMVar_hsa_circ_198538,RMVar_hsa_circ_198537,RMVar_hsa_circ_89951,RMVar_hsa_circ_68961,RMVar_hsa_circ_198548,RMVar_hsa_circ_198549,RMVar_hsa_circ_319411,RMVar_hsa_circ_320187,RMVar_hsa_circ_300588,RMVar_hsa_circ_72747,RMVar_hsa_circ_198550,RMVar_hsa_circ_12673,RMVar_hsa_circ_102276,RMVar_hsa_circ_330232,RMVar_hsa_circ_198558,RMVar_hsa_circ_103910,RMVar_hsa_circ_15468,RMVar_hsa_circ_22084,RMVar_hsa_circ_198560,RMVar_hsa_circ_198561,RMVar_hsa_circ_198562,RMVar_hsa_circ_88817,RMVar_hsa_circ_198563,RMVar_hsa_circ_87738,RMVar_hsa_circ_111691,RMVar_hsa_circ_198574,RMVar_hsa_circ_198575,RMVar_hsa_circ_300851,RMVar_hsa_circ_95380,RMVar_hsa_circ_198576,RMVar_hsa_circ_323671,RMVar_hsa_circ_330542,RMVar_hsa_circ_301453,RMVar_hsa_circ_66885,RMVar_hsa_circ_18567,RMVar_hsa_circ_198579,RMVar_hsa_circ_198580,RMVar_hsa_circ_198581,RMVar_hsa_circ_322879,RMVar_hsa_circ_98502,RMVar_hsa_circ_198586,RMVar_hsa_circ_304588,RMVar_hsa_circ_100039,RMVar_hsa_circ_38504,RMVar_hsa_circ_332667,RMVar_hsa_circ_101736,RMVar_hsa_circ_198592,RMVar_hsa_circ_198593,RMVar_hsa_circ_198594,RMVar_hsa_circ_94460,RMVar_hsa_circ_198595,RMVar_hsa_circ_111441,RMVar_hsa_circ_198596,RMVar_hsa_circ_198597,RMVar_hsa_circ_343827,RMVar_hsa_circ_351421,RMVar_hsa_circ_341055,RMVar_hsa_circ_52799,RMVar_hsa_circ_305393,RMVar_hsa_circ_275356,RMVar_hsa_circ_198599,RMVar_hsa_circ_198600 18947 RMVar_ID_18947 Human_SNP_ID_66132195 A-to-I Human chr2 + 32583915 32583915 32583915 ACCACGCCCGGCTAATTTTTTTGTATTTTTGTAGAGACGGAGGTTCGCCATGTTGGCCAGGCTGT ACCACGCCCGGCTAATTTTTTTGTATTTTTGTGGAGACGGAGGTTCGCCATGTTGGCCAGGCTGT A G BIRC6 Ensembl:ENSG00000115760 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs558747420 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51154,RMVar_hsa_circ_7021,RMVar_hsa_circ_75196,RMVar_hsa_circ_65955,RMVar_hsa_circ_99283,RMVar_hsa_circ_198494,RMVar_hsa_circ_111552,RMVar_hsa_circ_18585,RMVar_hsa_circ_198501,RMVar_hsa_circ_79240,RMVar_hsa_circ_198517,RMVar_hsa_circ_91605,RMVar_hsa_circ_198521,RMVar_hsa_circ_119573,RMVar_hsa_circ_198518,RMVar_hsa_circ_376028,RMVar_hsa_circ_121516,RMVar_hsa_circ_198523,RMVar_hsa_circ_198522,RMVar_hsa_circ_107594,RMVar_hsa_circ_198536,RMVar_hsa_circ_93776,RMVar_hsa_circ_84343,RMVar_hsa_circ_47300,RMVar_hsa_circ_99073,RMVar_hsa_circ_198538,RMVar_hsa_circ_198537,RMVar_hsa_circ_89951,RMVar_hsa_circ_68961,RMVar_hsa_circ_198548,RMVar_hsa_circ_198549,RMVar_hsa_circ_319411,RMVar_hsa_circ_320187,RMVar_hsa_circ_300588,RMVar_hsa_circ_72747,RMVar_hsa_circ_198550,RMVar_hsa_circ_12673,RMVar_hsa_circ_102276,RMVar_hsa_circ_330232,RMVar_hsa_circ_198558,RMVar_hsa_circ_103910,RMVar_hsa_circ_15468,RMVar_hsa_circ_22084,RMVar_hsa_circ_198560,RMVar_hsa_circ_198561,RMVar_hsa_circ_198562,RMVar_hsa_circ_88817,RMVar_hsa_circ_198563,RMVar_hsa_circ_87738,RMVar_hsa_circ_111691,RMVar_hsa_circ_198574,RMVar_hsa_circ_198575,RMVar_hsa_circ_300851,RMVar_hsa_circ_95380,RMVar_hsa_circ_198576,RMVar_hsa_circ_323671,RMVar_hsa_circ_330542,RMVar_hsa_circ_301453,RMVar_hsa_circ_66885,RMVar_hsa_circ_18567,RMVar_hsa_circ_198579,RMVar_hsa_circ_198580,RMVar_hsa_circ_198581,RMVar_hsa_circ_322879,RMVar_hsa_circ_98502,RMVar_hsa_circ_198586,RMVar_hsa_circ_304588,RMVar_hsa_circ_100039,RMVar_hsa_circ_38504,RMVar_hsa_circ_332667,RMVar_hsa_circ_101736,RMVar_hsa_circ_198592,RMVar_hsa_circ_198593,RMVar_hsa_circ_198594,RMVar_hsa_circ_94460,RMVar_hsa_circ_198595,RMVar_hsa_circ_111441,RMVar_hsa_circ_198596,RMVar_hsa_circ_198597,RMVar_hsa_circ_343827,RMVar_hsa_circ_351421,RMVar_hsa_circ_341055,RMVar_hsa_circ_52799,RMVar_hsa_circ_305393,RMVar_hsa_circ_275356,RMVar_hsa_circ_198599,RMVar_hsa_circ_198600 18948 RMVar_ID_18948 Human_SNP_ID_66132892 A-to-I Human chr2 + 32586548 32586548 32586548 ACCCAGAGCGATCCTCCCACCTTGACCCAAGTAGCTGGGACTACAGGCGTACACCACCACTCCCG ACCCAGAGCGATCCTCCCACCTTGACCCAAGTGGCTGGGACTACAGGCGTACACCACCACTCCCG A G BIRC6 Ensembl:ENSG00000115760 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1302630915 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25536564 RMVar_hsa_circ_51154,RMVar_hsa_circ_7021,RMVar_hsa_circ_75196,RMVar_hsa_circ_65955,RMVar_hsa_circ_99283,RMVar_hsa_circ_198494,RMVar_hsa_circ_111552,RMVar_hsa_circ_18585,RMVar_hsa_circ_198501,RMVar_hsa_circ_79240,RMVar_hsa_circ_198517,RMVar_hsa_circ_91605,RMVar_hsa_circ_198521,RMVar_hsa_circ_119573,RMVar_hsa_circ_198518,RMVar_hsa_circ_376028,RMVar_hsa_circ_121516,RMVar_hsa_circ_198523,RMVar_hsa_circ_198522,RMVar_hsa_circ_107594,RMVar_hsa_circ_198536,RMVar_hsa_circ_93776,RMVar_hsa_circ_84343,RMVar_hsa_circ_47300,RMVar_hsa_circ_99073,RMVar_hsa_circ_198538,RMVar_hsa_circ_198537,RMVar_hsa_circ_89951,RMVar_hsa_circ_68961,RMVar_hsa_circ_198548,RMVar_hsa_circ_198549,RMVar_hsa_circ_319411,RMVar_hsa_circ_320187,RMVar_hsa_circ_300588,RMVar_hsa_circ_72747,RMVar_hsa_circ_198550,RMVar_hsa_circ_12673,RMVar_hsa_circ_102276,RMVar_hsa_circ_330232,RMVar_hsa_circ_198558,RMVar_hsa_circ_103910,RMVar_hsa_circ_15468,RMVar_hsa_circ_22084,RMVar_hsa_circ_198560,RMVar_hsa_circ_198561,RMVar_hsa_circ_198562,RMVar_hsa_circ_88817,RMVar_hsa_circ_198563,RMVar_hsa_circ_87738,RMVar_hsa_circ_111691,RMVar_hsa_circ_198574,RMVar_hsa_circ_198575,RMVar_hsa_circ_300851,RMVar_hsa_circ_95380,RMVar_hsa_circ_198576,RMVar_hsa_circ_323671,RMVar_hsa_circ_330542,RMVar_hsa_circ_301453,RMVar_hsa_circ_66885,RMVar_hsa_circ_18567,RMVar_hsa_circ_198579,RMVar_hsa_circ_198580,RMVar_hsa_circ_198581,RMVar_hsa_circ_322879,RMVar_hsa_circ_98502,RMVar_hsa_circ_198586,RMVar_hsa_circ_304588,RMVar_hsa_circ_100039,RMVar_hsa_circ_38504,RMVar_hsa_circ_332667,RMVar_hsa_circ_101736,RMVar_hsa_circ_198592,RMVar_hsa_circ_198593,RMVar_hsa_circ_198594,RMVar_hsa_circ_94460,RMVar_hsa_circ_198595,RMVar_hsa_circ_111441,RMVar_hsa_circ_198596,RMVar_hsa_circ_198597,RMVar_hsa_circ_343827,RMVar_hsa_circ_351421,RMVar_hsa_circ_341055,RMVar_hsa_circ_52799,RMVar_hsa_circ_305393,RMVar_hsa_circ_275356,RMVar_hsa_circ_198599,RMVar_hsa_circ_198600 18949 RMVar_ID_18949 Human_SNP_ID_66140560 A-to-I Human chr2 + 32616402 32616402 32616402 CAAGAAGGCAAAACCCCGTCTCTACCAAAAACACAAAAAAATTAACTGGGCATGGTGGTGCATGC CAAGAAGGCAAAACCCCGTCTCTACCAAAAACCCAAAAAAATTAACTGGGCATGGTGGTGCATGC A C BIRC6 Ensembl:ENSG00000115760 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs905698842 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111552,RMVar_hsa_circ_198501,RMVar_hsa_circ_99073,RMVar_hsa_circ_198549,RMVar_hsa_circ_198599 18950 RMVar_ID_18950 Human_SNP_ID_66140561 A-to-I Human chr2 + 32616402 32616402 32616402 CAAGAAGGCAAAACCCCGTCTCTACCAAAAACACAAAAAAATTAACTGGGCATGGTGGTGCATGC CAAGAAGGCAAAACCCCGTCTCTACCAAAAACTCAAAAAAATTAACTGGGCATGGTGGTGCATGC A T BIRC6 Ensembl:ENSG00000115760 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs905698842 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111552,RMVar_hsa_circ_198501,RMVar_hsa_circ_99073,RMVar_hsa_circ_198549,RMVar_hsa_circ_198599 18951 RMVar_ID_18951 Human_SNP_ID_66140566 A-to-I Human chr2 + 32616421 32616421 32616421 CTCTACCAAAAACACAAAAAAATTAACTGGGCATGGTGGTGCATGCCTGTAATAGCAGTTGCTCG CTCTACCAAAAACACAAAAAAATTAACTGGGCGTGGTGGTGCATGCCTGTAATAGCAGTTGCTCG A G BIRC6 Ensembl:ENSG00000115760 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1023362226 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111552,RMVar_hsa_circ_198501,RMVar_hsa_circ_99073,RMVar_hsa_circ_198549,RMVar_hsa_circ_198599 18952 RMVar_ID_18952 Human_SNP_ID_66147894 A-to-I Human chr2 + 32642737 32642737 32642737 TTGCCCAGGCTGGAGTGCAGTGGCATGATCTCAGCTCACTGCAACCTCCACCTCCTGGGCTGAAG TTGCCCAGGCTGGAGTGCAGTGGCATGATCTCGGCTCACTGCAACCTCCACCTCCTGGGCTGAAG A G TTC27 Ensembl:ENSG00000018699 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1361364526 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13354,RMVar_hsa_circ_115979,RMVar_hsa_circ_358690,RMVar_hsa_circ_198609,RMVar_hsa_circ_371374,RMVar_hsa_circ_315761,RMVar_hsa_circ_304654,RMVar_hsa_circ_65543,RMVar_hsa_circ_110690,RMVar_hsa_circ_17729,RMVar_hsa_circ_198618,RMVar_hsa_circ_127570,RMVar_hsa_circ_198611,RMVar_hsa_circ_198613,RMVar_hsa_circ_198614,RMVar_hsa_circ_198612,RMVar_hsa_circ_326809,RMVar_hsa_circ_198610,RMVar_hsa_circ_374432,RMVar_hsa_circ_322641,RMVar_hsa_circ_274697,RMVar_hsa_circ_278252,RMVar_hsa_circ_272288,RMVar_hsa_circ_28529,RMVar_hsa_circ_78277,RMVar_hsa_circ_198620,RMVar_hsa_circ_198622,RMVar_hsa_circ_198621,RMVar_hsa_circ_198619,RMVar_hsa_circ_31882,RMVar_hsa_circ_198616,RMVar_hsa_circ_198617,RMVar_hsa_circ_342885,RMVar_hsa_circ_375805,RMVar_hsa_circ_45998,RMVar_hsa_circ_9986,RMVar_hsa_circ_29637,RMVar_hsa_circ_198624 18953 RMVar_ID_18953 Human_SNP_ID_66391452 A-to-I Human chr2 + 33534584 33534584 33534584 GGAGTCTTGCACTGTTGCCTGGGCTGGAGTGCAATGGTGCGATCTCGGCTCACTGAAACCTCCGC GGAGTCTTGCACTGTTGCCTGGGCTGGAGTGCGATGGTGCGATCTCGGCTCACTGAAACCTCCGC A G RASGRP3 Ensembl:ENSG00000152689 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1042852157 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19502,RMVar_hsa_circ_1303,RMVar_hsa_circ_268485,RMVar_hsa_circ_361163,RMVar_hsa_circ_351974,RMVar_hsa_circ_69902,RMVar_hsa_circ_57213,RMVar_hsa_circ_54129,RMVar_hsa_circ_32726,RMVar_hsa_circ_74052,RMVar_hsa_circ_198712 18954 RMVar_ID_18954 Human_SNP_ID_66392715 A-to-I Human chr2 + 33538924 33538923 33538925 AGCTGGGCGTGGTGGCACACACCTGTAGTCCTAGATACTTGGGAGGCTGAGGTGGAAGGATGGCT AGCTGGGCGTGGTGGCACACACCTGTAGTCCT__ATACTTGGGAGGCTGAGGTGGAAGGATGGCT TAG T RASGRP3 Ensembl:ENSG00000152689 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs774004323 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_19502,RMVar_hsa_circ_1303,RMVar_hsa_circ_268485,RMVar_hsa_circ_361163,RMVar_hsa_circ_351974,RMVar_hsa_circ_69902,RMVar_hsa_circ_57213,RMVar_hsa_circ_54129,RMVar_hsa_circ_32726,RMVar_hsa_circ_74052,RMVar_hsa_circ_198712 18955 RMVar_ID_18955 Human_SNP_ID_66392716 A-to-I Human chr2 + 33538924 33538923 33538924 AGCTGGGCGTGGTGGCACACACCTGTAGTCCTAGATACTTGGGAGGCTGAGGTGGAAGGATGGCT AGCTGGGCGTGGTGGCACACACCTGTAGTCCT_GATACTTGGGAGGCTGAGGTGGAAGGATGGCT TA T RASGRP3 Ensembl:ENSG00000152689 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1171126580 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_19502,RMVar_hsa_circ_1303,RMVar_hsa_circ_268485,RMVar_hsa_circ_361163,RMVar_hsa_circ_351974,RMVar_hsa_circ_69902,RMVar_hsa_circ_57213,RMVar_hsa_circ_54129,RMVar_hsa_circ_32726,RMVar_hsa_circ_74052,RMVar_hsa_circ_198712 18956 RMVar_ID_18956 Human_SNP_ID_66412454 A-to-I Human chr2 + 33607534 33607534 33607534 TAATTGGGGAAGTTGTATATCTTGTTACCTCCAGAATAAAGACTGGCAATCATTTATGTCTACAC TAATTGGGGAAGTTGTATATCTTGTTACCTCCGGAATAAAGACTGGCAATCATTTATGTCTACAC A G AC017050.1 Ensembl:ENSG00000286415 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1558556005 Functional Loss SNV dbSNP153 33..33 33 - - - 18957 RMVar_ID_18957 Human_SNP_ID_66480780 A-to-I Human chr2 - 33839969 33839969 33839969 GACTTCCTATCCATTTGACACCATTCGCCACCACATGATGATGCAGTCAGGGTGCAAAGGAACTG GACTTCCTATCCATTTGACACCATTCGCCACCTCATGATGATGCAGTCAGGGTGCAAAGGAACTG T A SLC25A5P2 Ensembl:ENSG00000235064 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs748537281 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1842595,Human_miRNA_ID_1905164 18958 RMVar_ID_18958 Human_SNP_ID_66480781 A-to-I Human chr2 - 33839969 33839969 33839969 GACTTCCTATCCATTTGACACCATTCGCCACCACATGATGATGCAGTCAGGGTGCAAAGGAACTG GACTTCCTATCCATTTGACACCATTCGCCACCGCATGATGATGCAGTCAGGGTGCAAAGGAACTG T C SLC25A5P2 Ensembl:ENSG00000235064 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs748537281 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1842595,Human_miRNA_ID_1905164 18959 RMVar_ID_18959 Human_SNP_ID_66480783 A-to-I Human chr2 - 33839972 33839972 33839972 GTTGACTTCCTATCCATTTGACACCATTCGCCACCACATGATGATGCAGTCAGGGTGCAAAGGAA GTTGACTTCCTATCCATTTGACACCATTCGCCGCCACATGATGATGCAGTCAGGGTGCAAAGGAA T C SLC25A5P2 Ensembl:ENSG00000235064 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs770153531 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1842595,Human_miRNA_ID_1905164 18960 RMVar_ID_18960 Human_SNP_ID_66480784 A-to-I Human chr2 - 33839972 33839972 33839972 GTTGACTTCCTATCCATTTGACACCATTCGCCACCACATGATGATGCAGTCAGGGTGCAAAGGAA GTTGACTTCCTATCCATTTGACACCATTCGCCCCCACATGATGATGCAGTCAGGGTGCAAAGGAA T G SLC25A5P2 Ensembl:ENSG00000235064 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs770153531 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1842595,Human_miRNA_ID_1905164 18961 RMVar_ID_18961 Human_SNP_ID_66480787 A-to-I Human chr2 - 33839979 33839979 33839979 TTGCTGGGTTGACTTCCTATCCATTTGACACCATTCGCCACCACATGATGATGCAGTCAGGGTGC TTGCTGGGTTGACTTCCTATCCATTTGACACCGTTCGCCACCACATGATGATGCAGTCAGGGTGC T C SLC25A5P2 Ensembl:ENSG00000235064 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs796462576 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1905164 18962 RMVar_ID_18962 Human_SNP_ID_66480840 A-to-I Human chr2 - 33840102 33840102 33840102 AGGGTATTATCATCTACCGAGCCGCCTACTTCAGTATCTATGACACTGCAAAGGGAATGCTTCCG AGGGTATTATCATCTACCGAGCCGCCTACTTCGGTATCTATGACACTGCAAAGGGAATGCTTCCG T C SLC25A5P2 Ensembl:ENSG00000235064 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878987725 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17393833,Human_RBP_ID_26482324 Human_miRNA_ID_1866562,Human_miRNA_ID_1866842 18963 RMVar_ID_18963 Human_SNP_ID_66480841 A-to-I Human chr2 - 33840102 33840102 33840102 AGGGTATTATCATCTACCGAGCCGCCTACTTCAGTATCTATGACACTGCAAAGGGAATGCTTCCG AGGGTATTATCATCTACCGAGCCGCCTACTTCCGTATCTATGACACTGCAAAGGGAATGCTTCCG T G SLC25A5P2 Ensembl:ENSG00000235064 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878987725 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17393833,Human_RBP_ID_26482324 Human_miRNA_ID_1866562,Human_miRNA_ID_1866842 18964 RMVar_ID_18964 Human_SNP_ID_67258810 A-to-I Human chr2 + 36504000 36504000 36504000 TCAAGCGATCCTCCCACCTGAGCCTCCCAAGTAACTGGGACTACAGGCACTGCCACCACACCCAG TCAAGCGATCCTCCCACCTGAGCCTCCCAAGTGACTGGGACTACAGGCACTGCCACCACACCCAG A G CRIM1 Ensembl:ENSG00000150938 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1187964563 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_374265,RMVar_hsa_circ_372113,RMVar_hsa_circ_275079,RMVar_hsa_circ_306421,RMVar_hsa_circ_80290,RMVar_hsa_circ_198741,RMVar_hsa_circ_198743,RMVar_hsa_circ_198742,RMVar_hsa_circ_198737,RMVar_hsa_circ_198739,RMVar_hsa_circ_198740,RMVar_hsa_circ_198738,RMVar_hsa_circ_291872,RMVar_hsa_circ_304850,RMVar_hsa_circ_372388,RMVar_hsa_circ_373984,RMVar_hsa_circ_111870,RMVar_hsa_circ_100634,RMVar_hsa_circ_126754,RMVar_hsa_circ_198755,RMVar_hsa_circ_89130,RMVar_hsa_circ_198757,RMVar_hsa_circ_198756,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_81508,RMVar_hsa_circ_198768,RMVar_hsa_circ_198769,RMVar_hsa_circ_198767,RMVar_hsa_circ_12447,RMVar_hsa_circ_198776,RMVar_hsa_circ_78338,RMVar_hsa_circ_283755,RMVar_hsa_circ_330071,RMVar_hsa_circ_198765,RMVar_hsa_circ_332230,RMVar_hsa_circ_104139,RMVar_hsa_circ_103881,RMVar_hsa_circ_198778,RMVar_hsa_circ_198779,RMVar_hsa_circ_198777,RMVar_hsa_circ_96900,RMVar_hsa_circ_317120,RMVar_hsa_circ_198774,RMVar_hsa_circ_198775,RMVar_hsa_circ_371470,RMVar_hsa_circ_277596,RMVar_hsa_circ_313176,RMVar_hsa_circ_126712,RMVar_hsa_circ_198784,RMVar_hsa_circ_198788,RMVar_hsa_circ_198789,RMVar_hsa_circ_198786,RMVar_hsa_circ_198787,RMVar_hsa_circ_198785,RMVar_hsa_circ_94432,RMVar_hsa_circ_370520,RMVar_hsa_circ_97131,RMVar_hsa_circ_80621,RMVar_hsa_circ_198799,RMVar_hsa_circ_198794,RMVar_hsa_circ_198796,RMVar_hsa_circ_198797,RMVar_hsa_circ_198795,RMVar_hsa_circ_282929,RMVar_hsa_circ_326951,RMVar_hsa_circ_321732,RMVar_hsa_circ_282278,RMVar_hsa_circ_82537,RMVar_hsa_circ_103055,RMVar_hsa_circ_198801,RMVar_hsa_circ_198802,RMVar_hsa_circ_198800,RMVar_hsa_circ_198798 18965 RMVar_ID_18965 Human_SNP_ID_67273384 A-to-I Human chr2 - 36553078 36553078 36553078 TCTGAGAGCTGGCTACCATTACCCTTCTTGCTATTGGAAACTCAGCACATTTGAACTTGGGTTTG TCTGAGAGCTGGCTACCATTACCCTTCTTGCTTTTGGAAACTCAGCACATTTGAACTTGGGTTTG T A FEZ2 Ensembl:ENSG00000171055 Protein coding intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs866354619 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_61696,Human_RBP_ID_550184,Human_RBP_ID_17507405 RMVar_hsa_circ_198827 18966 RMVar_ID_18966 Human_SNP_ID_67273385 A-to-I Human chr2 - 36553078 36553078 36553078 TCTGAGAGCTGGCTACCATTACCCTTCTTGCTATTGGAAACTCAGCACATTTGAACTTGGGTTTG TCTGAGAGCTGGCTACCATTACCCTTCTTGCTGTTGGAAACTCAGCACATTTGAACTTGGGTTTG T C FEZ2 Ensembl:ENSG00000171055 Protein coding intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs866354619 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_61696,Human_RBP_ID_550184,Human_RBP_ID_17507405 RMVar_hsa_circ_198827 18967 RMVar_ID_18967 Human_SNP_ID_67290813 A-to-I Human chr2 + 36604790 36604790 36604790 ATGAAACTAGCCAAACATGATGGCACACGCCTATAATCTCAGCCTCCCAAGTAGCTGAGACTACA ATGAAACTAGCCAAACATGATGGCACACGCCTGTAATCTCAGCCTCCCAAGTAGCTGAGACTACA A G L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs111693785 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9983128,Human_RBP_ID_13871969,Human_RBP_ID_22992346,Human_RBP_ID_25537814 18968 RMVar_ID_18968 Human_SNP_ID_67290821 A-to-I Human chr2 + 36604806 36604801 36604810 ATGATGGCACACGCCTATAATCTCAGCCTCCCAAGTAGCTGAGACTACAGGCGCCCGCCACCACG ATGATGGCACACGCCTATAATCTCAGCTACTCGGGAGGCTGAGACTACAGGCGCCCGCCACCACG CTCCCAAGTA TACTCGGGAG L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1558467427 Functional Loss MNV dbSNP153 28..37 33 - - - 18969 RMVar_ID_18969 Human_SNP_ID_67290824 A-to-I Human chr2 + 36604806 36604803 36604806 ATGATGGCACACGCCTATAATCTCAGCCTCCCAAGTAGCTGAGACTACAGGCGCCCGCCACCACG ATGATGGCACACGCCTATAATCTCAGCCTC___AGTAGCTGAGACTACAGGCGCCCGCCACCACG CCCA C L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1260915755 Functional Loss DEL dbSNP153 31..33 33 - - - 18970 RMVar_ID_18970 Human_SNP_ID_67290826 A-to-I Human chr2 + 36604806 36604804 36604806 ATGATGGCACACGCCTATAATCTCAGCCTCCCAAGTAGCTGAGACTACAGGCGCCCGCCACCACG ATGATGGCACACGCCTATAATCTCAGCCTCC__AGTAGCTGAGACTACAGGCGCCCGCCACCACG CCA C L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1558467436 Functional Loss DEL dbSNP153 32..33 33 - - - 18971 RMVar_ID_18971 Human_SNP_ID_67290830 A-to-I Human chr2 + 36604806 36604806 36604806 ATGATGGCACACGCCTATAATCTCAGCCTCCCAAGTAGCTGAGACTACAGGCGCCCGCCACCACG ATGATGGCACACGCCTATAATCTCAGCCTCCCGAGTAGCTGAGACTACAGGCGCCCGCCACCACG A G L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1486633282 Functional Loss SNV dbSNP153 33..33 33 - - - 18972 RMVar_ID_18972 Human_SNP_ID_67333128 A-to-I Human chr2 + 36760124 36760124 36760124 TCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGTGACTACAGGCACCTGCCACCACGCCCG TCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTGGCTGTGACTACAGGCACCTGCCACCACGCCCG A G VIT Ensembl:ENSG00000205221 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1354716650 Functional Loss SNV dbSNP153 33..33 33 - - - 18973 RMVar_ID_18973 Human_SNP_ID_67333622 A-to-I Human chr2 + 36761722 36761722 36761722 AGATCACGGCACTGCACTCCAGCCTGGGTGACAGAACGAGACTCCATCTAAAAAAAAAAGAAAAA AGATCACGGCACTGCACTCCAGCCTGGGTGACGGAACGAGACTCCATCTAAAAAAAAAAGAAAAA A G VIT Ensembl:ENSG00000205221 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1185593987 Functional Loss SNV dbSNP153 33..33 33 - - - 18974 RMVar_ID_18974 Human_SNP_ID_67334958 A-to-I Human chr2 + 36766458 36766458 36766458 GGAGGTTAGGTGGGAGGATCACTGTACCCCAGAAGTTCGAGGCTGCAGTGAGCTATAATTGTGCC GGAGGTTAGGTGGGAGGATCACTGTACCCCAGCAGTTCGAGGCTGCAGTGAGCTATAATTGTGCC A C VIT Ensembl:ENSG00000205221 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474315750 Functional Loss SNV dbSNP153 33..33 33 - - - 18975 RMVar_ID_18975 Human_SNP_ID_67369706 A-to-I Human chr2 - 36876249 36876249 36876249 TTTTTTTTTTTAAGGCAGGGTCTCACTCGGTCACCCAGGCTGGAGTGCAGTGGCTTGATCTCAGC TTTTTTTTTTTAAGGCAGGGTCTCACTCGGTCGCCCAGGCTGGAGTGCAGTGGCTTGATCTCAGC T C STRN Ensembl:ENSG00000115808 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs944159409 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14825,RMVar_hsa_circ_269293,RMVar_hsa_circ_368571,RMVar_hsa_circ_309030,RMVar_hsa_circ_198835,RMVar_hsa_circ_68842,RMVar_hsa_circ_198836,RMVar_hsa_circ_305662,RMVar_hsa_circ_12743,RMVar_hsa_circ_198839,RMVar_hsa_circ_198838,RMVar_hsa_circ_372726,RMVar_hsa_circ_348519,RMVar_hsa_circ_378047,RMVar_hsa_circ_17648,RMVar_hsa_circ_22386 18976 RMVar_ID_18976 Human_SNP_ID_67371725 A-to-I Human chr2 - 36882653 36882653 36882653 GTGATACTTCCACCTCAGCCTCCTGAGTAGCTAGGACTATAGGCACATGCCACCATGCCCAGATA GTGATACTTCCACCTCAGCCTCCTGAGTAGCTGGGACTATAGGCACATGCCACCATGCCCAGATA T C STRN Ensembl:ENSG00000115808 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs918933325 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14825,RMVar_hsa_circ_269293,RMVar_hsa_circ_309030,RMVar_hsa_circ_68842,RMVar_hsa_circ_198836,RMVar_hsa_circ_198843,RMVar_hsa_circ_12743,RMVar_hsa_circ_198839,RMVar_hsa_circ_372726,RMVar_hsa_circ_378047,RMVar_hsa_circ_17648,RMVar_hsa_circ_285695,RMVar_hsa_circ_336490,RMVar_hsa_circ_22386,RMVar_hsa_circ_350876,RMVar_hsa_circ_316222,RMVar_hsa_circ_289743,RMVar_hsa_circ_74814,RMVar_hsa_circ_281260,RMVar_hsa_circ_198844,RMVar_hsa_circ_198841,RMVar_hsa_circ_198842,RMVar_hsa_circ_198840 18977 RMVar_ID_18977 Human_SNP_ID_67377061 A-to-I Human chr2 - 36899989 36899989 36899989 AGCTGCTTGGGAGGCTGAAACTGGAGAATTGCATGAACCTGGGAGGCGGAGACTGGAGTGAGTTA AGCTGCTTGGGAGGCTGAAACTGGAGAATTGCCTGAACCTGGGAGGCGGAGACTGGAGTGAGTTA T G STRN Ensembl:ENSG00000115808 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1225679957 Functional Loss SNV dbSNP153 33..33 33 - - - 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_369113 18978 RMVar_ID_18978 Human_SNP_ID_67377266 A-to-I Human chr2 - 36900727 36900727 36900727 CACTACACCCAGCTAATTTTTGTATTTTTAGTAGAGATGGAGTTTCACCATGTTGGCTGGCCAGG CACTACACCCAGCTAATTTTTGTATTTTTAGTGGAGATGGAGTTTCACCATGTTGGCTGGCCAGG T C STRN Ensembl:ENSG00000115808 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1371098831 Functional Loss SNV dbSNP153 33..33 33 - - - 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_369113 18979 RMVar_ID_18979 Human_SNP_ID_67405423 A-to-I Human chr2 - 36991351 36991351 36991351 AGCTGGGATTACAAGCATGCACCACCATGCCCAGCTAATTTTGTGGTCAGGCTGGTCTCGAACTC AGCTGGGATTACAAGCATGCACCACCATGCCCGGCTAATTTTGTGGTCAGGCTGGTCTCGAACTC T C HEATR5B Ensembl:ENSG00000008869 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910967345 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35209,RMVar_hsa_circ_93250,RMVar_hsa_circ_90610,RMVar_hsa_circ_270079,RMVar_hsa_circ_316407,RMVar_hsa_circ_198854,RMVar_hsa_circ_330151,RMVar_hsa_circ_268461,RMVar_hsa_circ_50456,RMVar_hsa_circ_43101,RMVar_hsa_circ_291692,RMVar_hsa_circ_198857,RMVar_hsa_circ_198858,RMVar_hsa_circ_314513,RMVar_hsa_circ_323915,RMVar_hsa_circ_305989 18980 RMVar_ID_18980 Human_SNP_ID_67405660 A-to-I Human chr2 - 36992115 36992115 36992115 TGGCTCACTGCAACCTCTGCTTCCCGGATCCAAGCAATTCTGTAGCCTCAGCCTCCCAAATAGCT TGGCTCACTGCAACCTCTGCTTCCCGGATCCAGGCAATTCTGTAGCCTCAGCCTCCCAAATAGCT T C HEATR5B Ensembl:ENSG00000008869 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1302308401 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13873041 RMVar_hsa_circ_35209,RMVar_hsa_circ_93250,RMVar_hsa_circ_90610,RMVar_hsa_circ_270079,RMVar_hsa_circ_316407,RMVar_hsa_circ_198854,RMVar_hsa_circ_330151,RMVar_hsa_circ_268461,RMVar_hsa_circ_50456,RMVar_hsa_circ_43101,RMVar_hsa_circ_291692,RMVar_hsa_circ_198857,RMVar_hsa_circ_198858,RMVar_hsa_circ_314513,RMVar_hsa_circ_323915,RMVar_hsa_circ_305989 18981 RMVar_ID_18981 Human_SNP_ID_67408001 A-to-I Human chr2 - 36999756 36999756 36999756 GCCTGCCTTGGCCTCCCAAAGTTGCTAGCATTACAGACGTGAGCTACCGCACCCGGCCGGGAGGT GCCTGCCTTGGCCTCCCAAAGTTGCTAGCATTGCAGACGTGAGCTACCGCACCCGGCCGGGAGGT T C HEATR5B Ensembl:ENSG00000008869 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388533568 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35209,RMVar_hsa_circ_93250,RMVar_hsa_circ_90610,RMVar_hsa_circ_270079,RMVar_hsa_circ_316407,RMVar_hsa_circ_198854,RMVar_hsa_circ_330151,RMVar_hsa_circ_268461,RMVar_hsa_circ_50456,RMVar_hsa_circ_43101,RMVar_hsa_circ_291692,RMVar_hsa_circ_198857,RMVar_hsa_circ_198858,RMVar_hsa_circ_314513,RMVar_hsa_circ_323915,RMVar_hsa_circ_305989 18982 RMVar_ID_18982 Human_SNP_ID_67408003 A-to-I Human chr2 - 36999762 36999762 36999762 TGATCTGCCTGCCTTGGCCTCCCAAAGTTGCTAGCATTACAGACGTGAGCTACCGCACCCGGCCG TGATCTGCCTGCCTTGGCCTCCCAAAGTTGCTGGCATTACAGACGTGAGCTACCGCACCCGGCCG T C HEATR5B Ensembl:ENSG00000008869 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs530161657 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35209,RMVar_hsa_circ_93250,RMVar_hsa_circ_90610,RMVar_hsa_circ_270079,RMVar_hsa_circ_316407,RMVar_hsa_circ_198854,RMVar_hsa_circ_330151,RMVar_hsa_circ_268461,RMVar_hsa_circ_50456,RMVar_hsa_circ_43101,RMVar_hsa_circ_291692,RMVar_hsa_circ_198857,RMVar_hsa_circ_198858,RMVar_hsa_circ_314513,RMVar_hsa_circ_323915,RMVar_hsa_circ_305989 18983 RMVar_ID_18983 Human_SNP_ID_67413424 A-to-I Human chr2 - 37017341 37017341 37017341 TTGCCCAGGCTGTAGTGCAGTGGCATGATCTCAGCTCACTGCACCCTCCGCCTCCCGAGTTCAAG TTGCCCAGGCTGTAGTGCAGTGGCATGATCTCGGCTCACTGCACCCTCCGCCTCCCGAGTTCAAG T C HEATR5B Ensembl:ENSG00000008869 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1446716487 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7912,RMVar_hsa_circ_35209,RMVar_hsa_circ_93250,RMVar_hsa_circ_90610,RMVar_hsa_circ_270079,RMVar_hsa_circ_198854,RMVar_hsa_circ_268461,RMVar_hsa_circ_198858,RMVar_hsa_circ_314513,RMVar_hsa_circ_323915,RMVar_hsa_circ_327191,RMVar_hsa_circ_344023,RMVar_hsa_circ_324544,RMVar_hsa_circ_302550,RMVar_hsa_circ_83343,RMVar_hsa_circ_102171,RMVar_hsa_circ_111754,RMVar_hsa_circ_100689,RMVar_hsa_circ_61485,RMVar_hsa_circ_42740,RMVar_hsa_circ_46783,RMVar_hsa_circ_80815,RMVar_hsa_circ_198860,RMVar_hsa_circ_198864,RMVar_hsa_circ_198865,RMVar_hsa_circ_198862,RMVar_hsa_circ_198863,RMVar_hsa_circ_198861,RMVar_hsa_circ_124124,RMVar_hsa_circ_198859,RMVar_hsa_circ_328621,RMVar_hsa_circ_287825,RMVar_hsa_circ_102376,RMVar_hsa_circ_37224,RMVar_hsa_circ_198873,RMVar_hsa_circ_198874,RMVar_hsa_circ_198875,RMVar_hsa_circ_198872,RMVar_hsa_circ_326911,RMVar_hsa_circ_325069,RMVar_hsa_circ_49424,RMVar_hsa_circ_80947,RMVar_hsa_circ_126204,RMVar_hsa_circ_198877,RMVar_hsa_circ_198876,RMVar_hsa_circ_198881,RMVar_hsa_circ_90596,RMVar_hsa_circ_318818,RMVar_hsa_circ_198880,RMVar_hsa_circ_58063,RMVar_hsa_circ_198883,RMVar_hsa_circ_198884,RMVar_hsa_circ_266586,RMVar_hsa_circ_342971,RMVar_hsa_circ_65590,RMVar_hsa_circ_198885,RMVar_hsa_circ_198889,RMVar_hsa_circ_102955,RMVar_hsa_circ_294418,RMVar_hsa_circ_329630,RMVar_hsa_circ_363724,RMVar_hsa_circ_327072,RMVar_hsa_circ_282653,RMVar_hsa_circ_33735,RMVar_hsa_circ_25404,RMVar_hsa_circ_198890,RMVar_hsa_circ_198887,RMVar_hsa_circ_198888,RMVar_hsa_circ_198886 18984 RMVar_ID_18984 Human_SNP_ID_67422706 A-to-I Human chr2 - 37048325 37048325 37048325 CAGAAATTAGCTGGGCATGGTTGAATATACCTATCGTCCCATCTACTTGGGAGGCTGAGATGGGA CAGAAATTAGCTGGGCATGGTTGAATATACCTTTCGTCCCATCTACTTGGGAGGCTGAGATGGGA T A HEATR5B Ensembl:ENSG00000008869 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs966012980 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16820,RMVar_hsa_circ_7912,RMVar_hsa_circ_93250,RMVar_hsa_circ_90610,RMVar_hsa_circ_198854,RMVar_hsa_circ_268461,RMVar_hsa_circ_198858,RMVar_hsa_circ_324544,RMVar_hsa_circ_83343,RMVar_hsa_circ_111754,RMVar_hsa_circ_100689,RMVar_hsa_circ_80815,RMVar_hsa_circ_198860,RMVar_hsa_circ_198861,RMVar_hsa_circ_124124,RMVar_hsa_circ_198859,RMVar_hsa_circ_102376,RMVar_hsa_circ_198873,RMVar_hsa_circ_198874,RMVar_hsa_circ_198875,RMVar_hsa_circ_325069,RMVar_hsa_circ_49424,RMVar_hsa_circ_80947,RMVar_hsa_circ_126204,RMVar_hsa_circ_198876,RMVar_hsa_circ_198881,RMVar_hsa_circ_58063,RMVar_hsa_circ_198884,RMVar_hsa_circ_266586,RMVar_hsa_circ_24707,RMVar_hsa_circ_198885,RMVar_hsa_circ_102955,RMVar_hsa_circ_363724,RMVar_hsa_circ_25404,RMVar_hsa_circ_198886,RMVar_hsa_circ_72741,RMVar_hsa_circ_338623,RMVar_hsa_circ_73569,RMVar_hsa_circ_48707,RMVar_hsa_circ_198893,RMVar_hsa_circ_121775,RMVar_hsa_circ_15405,RMVar_hsa_circ_198896,RMVar_hsa_circ_85900,RMVar_hsa_circ_327180,RMVar_hsa_circ_322309,RMVar_hsa_circ_95138,RMVar_hsa_circ_18790,RMVar_hsa_circ_84975,RMVar_hsa_circ_198897,RMVar_hsa_circ_198899,RMVar_hsa_circ_198898,RMVar_hsa_circ_339802,RMVar_hsa_circ_351280,RMVar_hsa_circ_368307,RMVar_hsa_circ_315415,RMVar_hsa_circ_104956,RMVar_hsa_circ_112168,RMVar_hsa_circ_104776,RMVar_hsa_circ_76053,RMVar_hsa_circ_51090,RMVar_hsa_circ_31473,RMVar_hsa_circ_198902,RMVar_hsa_circ_198906,RMVar_hsa_circ_198908,RMVar_hsa_circ_198907,RMVar_hsa_circ_198904,RMVar_hsa_circ_198905,RMVar_hsa_circ_198903,RMVar_hsa_circ_80714,RMVar_hsa_circ_292110,RMVar_hsa_circ_349270,RMVar_hsa_circ_198901,RMVar_hsa_circ_346944,RMVar_hsa_circ_51742,RMVar_hsa_circ_198916,RMVar_hsa_circ_125745,RMVar_hsa_circ_198913,RMVar_hsa_circ_198914,RMVar_hsa_circ_305344,RMVar_hsa_circ_198912,RMVar_hsa_circ_302395,RMVar_hsa_circ_373793,RMVar_hsa_circ_1710,RMVar_hsa_circ_73709,RMVar_hsa_circ_198917 18985 RMVar_ID_18985 Human_SNP_ID_67422707 A-to-I Human chr2 - 37048325 37048325 37048325 CAGAAATTAGCTGGGCATGGTTGAATATACCTATCGTCCCATCTACTTGGGAGGCTGAGATGGGA CAGAAATTAGCTGGGCATGGTTGAATATACCTGTCGTCCCATCTACTTGGGAGGCTGAGATGGGA T C HEATR5B Ensembl:ENSG00000008869 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs966012980 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16820,RMVar_hsa_circ_7912,RMVar_hsa_circ_93250,RMVar_hsa_circ_90610,RMVar_hsa_circ_198854,RMVar_hsa_circ_268461,RMVar_hsa_circ_198858,RMVar_hsa_circ_324544,RMVar_hsa_circ_83343,RMVar_hsa_circ_111754,RMVar_hsa_circ_100689,RMVar_hsa_circ_80815,RMVar_hsa_circ_198860,RMVar_hsa_circ_198861,RMVar_hsa_circ_124124,RMVar_hsa_circ_198859,RMVar_hsa_circ_102376,RMVar_hsa_circ_198873,RMVar_hsa_circ_198874,RMVar_hsa_circ_198875,RMVar_hsa_circ_325069,RMVar_hsa_circ_49424,RMVar_hsa_circ_80947,RMVar_hsa_circ_126204,RMVar_hsa_circ_198876,RMVar_hsa_circ_198881,RMVar_hsa_circ_58063,RMVar_hsa_circ_198884,RMVar_hsa_circ_266586,RMVar_hsa_circ_24707,RMVar_hsa_circ_198885,RMVar_hsa_circ_102955,RMVar_hsa_circ_363724,RMVar_hsa_circ_25404,RMVar_hsa_circ_198886,RMVar_hsa_circ_72741,RMVar_hsa_circ_338623,RMVar_hsa_circ_73569,RMVar_hsa_circ_48707,RMVar_hsa_circ_198893,RMVar_hsa_circ_121775,RMVar_hsa_circ_15405,RMVar_hsa_circ_198896,RMVar_hsa_circ_85900,RMVar_hsa_circ_327180,RMVar_hsa_circ_322309,RMVar_hsa_circ_95138,RMVar_hsa_circ_18790,RMVar_hsa_circ_84975,RMVar_hsa_circ_198897,RMVar_hsa_circ_198899,RMVar_hsa_circ_198898,RMVar_hsa_circ_339802,RMVar_hsa_circ_351280,RMVar_hsa_circ_368307,RMVar_hsa_circ_315415,RMVar_hsa_circ_104956,RMVar_hsa_circ_112168,RMVar_hsa_circ_104776,RMVar_hsa_circ_76053,RMVar_hsa_circ_51090,RMVar_hsa_circ_31473,RMVar_hsa_circ_198902,RMVar_hsa_circ_198906,RMVar_hsa_circ_198908,RMVar_hsa_circ_198907,RMVar_hsa_circ_198904,RMVar_hsa_circ_198905,RMVar_hsa_circ_198903,RMVar_hsa_circ_80714,RMVar_hsa_circ_292110,RMVar_hsa_circ_349270,RMVar_hsa_circ_198901,RMVar_hsa_circ_346944,RMVar_hsa_circ_51742,RMVar_hsa_circ_198916,RMVar_hsa_circ_125745,RMVar_hsa_circ_198913,RMVar_hsa_circ_198914,RMVar_hsa_circ_305344,RMVar_hsa_circ_198912,RMVar_hsa_circ_302395,RMVar_hsa_circ_373793,RMVar_hsa_circ_1710,RMVar_hsa_circ_73709,RMVar_hsa_circ_198917 18986 RMVar_ID_18986 Human_SNP_ID_67437458 A-to-I Human chr2 - 37100446 37100446 37100446 CTTCTCAAATCTGTGTGGCTCTTATGGGGTTAATTTGATTTGGACCTGTATTAATTTCTTATGGC CTTCTCAAATCTGTGTGGCTCTTATGGGGTTAGTTTGATTTGGACCTGTATTAATTTCTTATGGC T C EIF2AK2 Ensembl:ENSG00000055332 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs10697 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3624732 Human_miRNA_ID_1130391 18987 RMVar_ID_18987 Human_SNP_ID_67437473 A-to-I Human chr2 - 37100519 37100519 37100519 GGTGACATTATTGGCTTAAATTCTAAATAACTAGAAACTGTATAATAGGCAAAACTGTGAGGCAA GGTGACATTATTGGCTTAAATTCTAAATAACTGGAAACTGTATAATAGGCAAAACTGTGAGGCAA T C EIF2AK2 Ensembl:ENSG00000055332 Protein coding 3'UTR GSE38233;GSE100210;GSE112787 cultured B-cells;HepG2 cell line;293 Flip-In T-REx cells,empty vector - 24183664,29129909,29967493 RNA-Seq:(High) rs14041 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18316747 18988 RMVar_ID_18988 Human_SNP_ID_67437474 A-to-I Human chr2 - 37100523 37100523 37100523 ATATGGTGACATTATTGGCTTAAATTCTAAATAACTAGAAACTGTATAATAGGCAAAACTGTGAG ATATGGTGACATTATTGGCTTAAATTCTAAATGACTAGAAACTGTATAATAGGCAAAACTGTGAG T C EIF2AK2 Ensembl:ENSG00000055332 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1558401528 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18316747 18989 RMVar_ID_18989 Human_SNP_ID_67437476 A-to-I Human chr2 - 37100534 37100534 37100534 AGTTGATAGTTATATGGTGACATTATTGGCTTAAATTCTAAATAACTAGAAACTGTATAATAGGC AGTTGATAGTTATATGGTGACATTATTGGCTTCAATTCTAAATAACTAGAAACTGTATAATAGGC T G EIF2AK2 Ensembl:ENSG00000055332 Protein coding 3'UTR GSE38233;GSE107867 cultured B-cells;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 24183664,30559470 RNA-Seq:(High) rs905798033 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18316747 18990 RMVar_ID_18990 Human_SNP_ID_67437558 A-to-I Human chr2 - 37100891 37100891 37100891 TGTATTTGAGGGGTACTTTGTCTCACACTTTTACCTGTTACATGGTTTTCAGTAATTTAGAATTT TGTATTTGAGGGGTACTTTGTCTCACACTTTTTCCTGTTACATGGTTTTCAGTAATTTAGAATTT T A EIF2AK2 Ensembl:ENSG00000055332 Protein coding 3'UTR GSE100210;GSE112787 HepG2 cell line;293 Flip-In T-REx cells,empty vector - 29129909,29967493 RNA-Seq:(High) rs552562330 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1163806,Human_miRNA_ID_1217839 18991 RMVar_ID_18991 Human_SNP_ID_67437566 A-to-I Human chr2 - 37100944 37100944 37100944 TGATGCCATTCAAGTAAATACAAGTCTCAGTCAGATGAACCCCAAGAGCCACATGTATTTGAGGG TGATGCCATTCAAGTAAATACAAGTCTCAGTCTGATGAACCCCAAGAGCCACATGTATTTGAGGG T A EIF2AK2 Ensembl:ENSG00000055332 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs112433864 Functional Loss SNV dbSNP153 33..33 33 - - - 18992 RMVar_ID_18992 Human_SNP_ID_67437567 A-to-I Human chr2 - 37100944 37100944 37100944 TGATGCCATTCAAGTAAATACAAGTCTCAGTCAGATGAACCCCAAGAGCCACATGTATTTGAGGG TGATGCCATTCAAGTAAATACAAGTCTCAGTCGGATGAACCCCAAGAGCCACATGTATTTGAGGG T C EIF2AK2 Ensembl:ENSG00000055332 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs112433864 Functional Loss SNV dbSNP153 33..33 33 - - - 18993 RMVar_ID_18993 Human_SNP_ID_67437570 A-to-I Human chr2 - 37100954 37100954 37100954 AGCAGGATTCTGATGCCATTCAAGTAAATACAAGTCTCAGTCAGATGAACCCCAAGAGCCACATG AGCAGGATTCTGATGCCATTCAAGTAAATACAGGTCTCAGTCAGATGAACCCCAAGAGCCACATG T C EIF2AK2 Ensembl:ENSG00000055332 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs111521470 Functional Loss SNV dbSNP153 33..33 33 - - - 18994 RMVar_ID_18994 Human_SNP_ID_67437610 A-to-I Human chr2 - 37101146 37101146 37101146 AACCAATACTTTGAAACTAGCATGTTTAGAATAGAGCAGGAGGAAACTATATTTGAAAGGTCAGA AACCAATACTTTGAAACTAGCATGTTTAGAATGGAGCAGGAGGAAACTATATTTGAAAGGTCAGA T C EIF2AK2 Ensembl:ENSG00000055332 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1301142746 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6915938,Human_RBP_ID_13873566 18995 RMVar_ID_18995 Human_SNP_ID_67437817 A-to-I Human chr2 - 37102074 37102074 37102074 CAACACACCCAACTAATTTTTAAATTTTTTGTAGAAATATGGTCTTGCTGTGTTTCCCAGGCTGG CAACACACCCAACTAATTTTTAAATTTTTTGTGGAAATATGGTCTTGCTGTGTTTCCCAGGCTGG T C EIF2AK2 Ensembl:ENSG00000055332 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1468693404 Functional Loss SNV dbSNP153 33..33 33 - - - 18996 RMVar_ID_18996 Human_SNP_ID_67437825 A-to-I Human chr2 - 37102092 37102092 37102092 GGGACTACATGCATACACCAACACACCCAACTAATTTTTAAATTTTTTGTAGAAATATGGTCTTG GGGACTACATGCATACACCAACACACCCAACTCATTTTTAAATTTTTTGTAGAAATATGGTCTTG T G EIF2AK2 Ensembl:ENSG00000055332 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs894561971 Functional Loss SNV dbSNP153 33..33 33 - - - 18997 RMVar_ID_18997 Human_SNP_ID_67437843 A-to-I Human chr2 - 37102153 37102153 37102153 TCCTTGTAACCTCGAACTCCTAGGCTCAAGTGATCCTCCTGCCTCAGCCGCTTGAATAGCTGGGA TCCTTGTAACCTCGAACTCCTAGGCTCAAGTGTTCCTCCTGCCTCAGCCGCTTGAATAGCTGGGA T A EIF2AK2 Ensembl:ENSG00000055332 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903210064 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_235672 18998 RMVar_ID_18998 Human_SNP_ID_67437844 A-to-I Human chr2 - 37102164 37102164 37102164 ACGATCACAGCTCCTTGTAACCTCGAACTCCTAGGCTCAAGTGATCCTCCTGCCTCAGCCGCTTG ACGATCACAGCTCCTTGTAACCTCGAACTCCTGGGCTCAAGTGATCCTCCTGCCTCAGCCGCTTG T C EIF2AK2 Ensembl:ENSG00000055332 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs999281622 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_235672 18999 RMVar_ID_18999 Human_SNP_ID_67437868 A-to-I Human chr2 - 37102226 37102226 37102226 ATTGTAATTTTTTTTTTAAGAGACAGGATCTCACTCTGTCACCCAGGCCAGAGTACAGTGGTACG ATTGTAATTTTTTTTTTAAGAGACAGGATCTCTCTCTGTCACCCAGGCCAGAGTACAGTGGTACG T A EIF2AK2 Ensembl:ENSG00000055332 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1300867902 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_235672 19000 RMVar_ID_19000 Human_SNP_ID_67438111 A-to-I Human chr2 - 37103293 37103293 37103293 TACTCGGGAGTCCGTGGCAGGAGAATCGCTTGAACCCAGGAGGTGGAGGTTGCAGTGAGCTGAGA TACTCGGGAGTCCGTGGCAGGAGAATCGCTTGGACCCAGGAGGTGGAGGTTGCAGTGAGCTGAGA T C EIF2AK2 Ensembl:ENSG00000055332 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,31158229,31158229,31158229 RNA-Seq:(High) rs1012238080 Functional Loss SNV dbSNP153 33..33 33 - - - 19001 RMVar_ID_19001 Human_SNP_ID_67438123 A-to-I Human chr2 - 37103333 37103318 37103333 AAATTAGCTGGGTGTGGTGGTAGGCGCCTGTAATCCCAGCTACTCGGGAGTCCGTGGCAGGAGAA AAATTAGCTGGGTGTGGTGGTAGGCGCCTGTA_______________GAGTCCGTGGCAGGAGAA CCCGAGTAGCTGGGAT C EIF2AK2 Ensembl:ENSG00000055332 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167238653 Functional Loss DEL dbSNP153 33..47 33 - - - 19002 RMVar_ID_19002 Human_SNP_ID_67438128 A-to-I Human chr2 - 37103333 37103333 37103333 AAATTAGCTGGGTGTGGTGGTAGGCGCCTGTAATCCCAGCTACTCGGGAGTCCGTGGCAGGAGAA AAATTAGCTGGGTGTGGTGGTAGGCGCCTGTAGTCCCAGCTACTCGGGAGTCCGTGGCAGGAGAA T C EIF2AK2 Ensembl:ENSG00000055332 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1553333747 Functional Loss SNV dbSNP153 33..33 33 - - - 19003 RMVar_ID_19003 Human_SNP_ID_67438134 A-to-I Human chr2 - 37103344 37103344 37103344 TAAAAATACAAAAATTAGCTGGGTGTGGTGGTAGGCGCCTGTAATCCCAGCTACTCGGGAGTCCG TAAAAATACAAAAATTAGCTGGGTGTGGTGGTGGGCGCCTGTAATCCCAGCTACTCGGGAGTCCG T C EIF2AK2 Ensembl:ENSG00000055332 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs183221906 Functional Loss SNV dbSNP153 33..33 33 - - - 19004 RMVar_ID_19004 Human_SNP_ID_67438168 A-to-I Human chr2 - 37103471 37103471 37103471 CCTACTCTGGCTGGGCATGGTGGCTCACGCCTATAATCCCAGCACTCTGGGAGGCCGAGACGGGT CCTACTCTGGCTGGGCATGGTGGCTCACGCCTTTAATCCCAGCACTCTGGGAGGCCGAGACGGGT T A EIF2AK2 Ensembl:ENSG00000055332 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs770357644 Functional Loss SNV dbSNP153 33..33 33 - - - 19005 RMVar_ID_19005 Human_SNP_ID_67438169 A-to-I Human chr2 - 37103471 37103471 37103471 CCTACTCTGGCTGGGCATGGTGGCTCACGCCTATAATCCCAGCACTCTGGGAGGCCGAGACGGGT CCTACTCTGGCTGGGCATGGTGGCTCACGCCTGTAATCCCAGCACTCTGGGAGGCCGAGACGGGT T C EIF2AK2 Ensembl:ENSG00000055332 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs770357644 Functional Loss SNV dbSNP153 33..33 33 - - - 19006 RMVar_ID_19006 Human_SNP_ID_67438266 A-to-I Human chr2 - 37103895 37103895 37103895 ACCTCAGGTGATTCACTTGCCTTGGCCTCCCAAAGTGTTGAGATTACAGGCATGAGTCACTGCAC ACCTCAGGTGATTCACTTGCCTTGGCCTCCCATAGTGTTGAGATTACAGGCATGAGTCACTGCAC T A EIF2AK2 Ensembl:ENSG00000055332 Protein coding 3'UTR GSE38233;GSE100210;GSE112787 cultured B-cells;HepG2 cell line;293 Flip-In T-REx cells,empty vector - 24183664,29129909,29967493 RNA-Seq:(High) rs1417658485 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23182711 19007 RMVar_ID_19007 Human_SNP_ID_67438272 A-to-I Human chr2 - 37103927 37103927 37103927 ACCATGTTGACCCAGCTGGTTTTGAACTCCTGACCTCAGGTGATTCACTTGCCTTGGCCTCCCAA ACCATGTTGACCCAGCTGGTTTTGAACTCCTGCCCTCAGGTGATTCACTTGCCTTGGCCTCCCAA T G EIF2AK2 Ensembl:ENSG00000055332 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1166868868 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25538438 19008 RMVar_ID_19008 Human_SNP_ID_67438273 A-to-I Human chr2 - 37103935 37103935 37103935 GGAATTTCACCATGTTGACCCAGCTGGTTTTGAACTCCTGACCTCAGGTGATTCACTTGCCTTGG GGAATTTCACCATGTTGACCCAGCTGGTTTTGTACTCCTGACCTCAGGTGATTCACTTGCCTTGG T A EIF2AK2 Ensembl:ENSG00000055332 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1310525381 Functional Loss SNV dbSNP153 33..33 33 - - - 19009 RMVar_ID_19009 Human_SNP_ID_67438279 A-to-I Human chr2 - 37103971 37103971 37103971 CACTCCAGGTTAATTTTTTCTATTTTTAGTAGAGACGGAATTTCACCATGTTGACCCAGCTGGTT CACTCCAGGTTAATTTTTTCTATTTTTAGTAGCGACGGAATTTCACCATGTTGACCCAGCTGGTT T G EIF2AK2 Ensembl:ENSG00000055332 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1449534831 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13873595 19010 RMVar_ID_19010 Human_SNP_ID_67438282 A-to-I Human chr2 - 37103982 37103982 37103982 GTATCTGCCACCACTCCAGGTTAATTTTTTCTATTTTTAGTAGAGACGGAATTTCACCATGTTGA GTATCTGCCACCACTCCAGGTTAATTTTTTCTGTTTTTAGTAGAGACGGAATTTCACCATGTTGA T C EIF2AK2 Ensembl:ENSG00000055332 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1464178248 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6915977,Human_RBP_ID_26487092 19011 RMVar_ID_19011 Human_SNP_ID_67438283 A-to-I Human chr2 - 37103992 37103992 37103992 GGGATTACAGGTATCTGCCACCACTCCAGGTTAATTTTTTCTATTTTTAGTAGAGACGGAATTTC GGGATTACAGGTATCTGCCACCACTCCAGGTTGATTTTTTCTATTTTTAGTAGAGACGGAATTTC T C EIF2AK2 Ensembl:ENSG00000055332 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048694092 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6915977,Human_RBP_ID_26487092 19012 RMVar_ID_19012 Human_SNP_ID_67438381 A-to-I Human chr2 - 37104412 37104412 37104412 GGGGGGGTGAGGTGGGAGGATCACTTGAGCCTAGGAGGTCAAGGCCGCAGTGAGCCATGATCATG GGGGGGGTGAGGTGGGAGGATCACTTGAGCCTCGGAGGTCAAGGCCGCAGTGAGCCATGATCATG T G EIF2AK2 Ensembl:ENSG00000055332 Protein coding 3'UTR GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line - 24183664,31158229 RNA-Seq:(High) rs1308382747 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_827933,Human_RBP_ID_25538441 19013 RMVar_ID_19013 Human_SNP_ID_67438408 A-to-I Human chr2 - 37104499 37104499 37104499 CCTGGGCAACACAGTGAGTTCTCATCTCTACAAAAAATCAGAAAATTAGCTGGGCATGGTAGTGT CCTGGGCAACACAGTGAGTTCTCATCTCTACAGAAAATCAGAAAATTAGCTGGGCATGGTAGTGT T C EIF2AK2 Ensembl:ENSG00000055332 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1340126534 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6915984 19014 RMVar_ID_19014 Human_SNP_ID_67438426 A-to-I Human chr2 - 37104602 37104602 37104602 TTTAAAAAGACAAAAGCTGGACGCAGTAGCTAATGCCTGTTATCCCAGCATTTTTGGGAGGTCAA TTTAAAAAGACAAAAGCTGGACGCAGTAGCTAGTGCCTGTTATCCCAGCATTTTTGGGAGGTCAA T C EIF2AK2 Ensembl:ENSG00000055332 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1318618387 Functional Loss SNV dbSNP153 33..33 33 - - - 19015 RMVar_ID_19015 Human_SNP_ID_67438428 A-to-I Human chr2 - 37104607 37104607 37104607 GGATATTTAAAAAGACAAAAGCTGGACGCAGTAGCTAATGCCTGTTATCCCAGCATTTTTGGGAG GGATATTTAAAAAGACAAAAGCTGGACGCAGTGGCTAATGCCTGTTATCCCAGCATTTTTGGGAG T C EIF2AK2 Ensembl:ENSG00000055332 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs910612917 Functional Loss SNV dbSNP153 33..33 33 - - - 19016 RMVar_ID_19016 Human_SNP_ID_67438546 A-to-I Human chr2 - 37105138 37105138 37105138 TTTAAAAAGGGCCAAATTTAGGTTAAGCAAAAAGTGAAAATACAGTAAGAGAAAATAGTTTTATA TTTAAAAAGGGCCAAATTTAGGTTAAGCAAAAGGTGAAAATACAGTAAGAGAAAATAGTTTTATA T C EIF2AK2 Ensembl:ENSG00000055332 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1023679615 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_183509 19017 RMVar_ID_19017 Human_SNP_ID_67438547 A-to-I Human chr2 - 37105138 37105138 37105138 TTTAAAAAGGGCCAAATTTAGGTTAAGCAAAAAGTGAAAATACAGTAAGAGAAAATAGTTTTATA TTTAAAAAGGGCCAAATTTAGGTTAAGCAAAACGTGAAAATACAGTAAGAGAAAATAGTTTTATA T G EIF2AK2 Ensembl:ENSG00000055332 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1023679615 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_183509 19018 RMVar_ID_19018 Human_SNP_ID_67441738 A-to-I Human chr2 - 37117029 37117029 37117029 TTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCAAGGTTGGCCTTGGACTGATGGGCC TTTTGTATTTTTAGTAGAGACAGGGTTTCACCGTGTTGGCAAGGTTGGCCTTGGACTGATGGGCC T C EIF2AK2 Ensembl:ENSG00000055332 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs774752293 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13873728 RMVar_hsa_circ_8460,RMVar_hsa_circ_59790,RMVar_hsa_circ_66968,RMVar_hsa_circ_48602,RMVar_hsa_circ_376240,RMVar_hsa_circ_38492,RMVar_hsa_circ_352412,RMVar_hsa_circ_11694,RMVar_hsa_circ_198953 19019 RMVar_ID_19019 Human_SNP_ID_67443649 A-to-I Human chr2 - 37123313 37123313 37123313 GCAATGAGCCAAGATTGTGCCACTGCACTCCAACCTGGGTGACAGAGCAAGACTCTGTCTCAATA GCAATGAGCCAAGATTGTGCCACTGCACTCCAGCCTGGGTGACAGAGCAAGACTCTGTCTCAATA T C EIF2AK2 Ensembl:ENSG00000055332 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1459890285 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8460,RMVar_hsa_circ_59790,RMVar_hsa_circ_48602,RMVar_hsa_circ_376240,RMVar_hsa_circ_38492,RMVar_hsa_circ_11694,RMVar_hsa_circ_341163,RMVar_hsa_circ_361268,RMVar_hsa_circ_198953,RMVar_hsa_circ_352994,RMVar_hsa_circ_65515,RMVar_hsa_circ_68099 19020 RMVar_ID_19020 Human_SNP_ID_67447812 A-to-I Human chr2 - 37138838 37138838 37138838 TGAGCCAAGATTGTGCCACTGCACTTCAACCTAGACAACAGAGCCAGATCCTGTCTGAAAAGAAA TGAGCCAAGATTGTGCCACTGCACTTCAACCTGGACAACAGAGCCAGATCCTGTCTGAAAAGAAA T C EIF2AK2 Ensembl:ENSG00000055332 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1345819154 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48602,RMVar_hsa_circ_13772,RMVar_hsa_circ_341163,RMVar_hsa_circ_32277,RMVar_hsa_circ_122724,RMVar_hsa_circ_93727,RMVar_hsa_circ_198955,RMVar_hsa_circ_49371,RMVar_hsa_circ_198956,RMVar_hsa_circ_6737 19021 RMVar_ID_19021 Human_SNP_ID_67447954 A-to-I Human chr2 - 37139215 37139215 37139215 CGCCTCCCATGTTCAAGCAATTCTCCTGCCTCAGCCTACTGAGTAGCTGGGACTACAAGCGCCTG CGCCTCCCATGTTCAAGCAATTCTCCTGCCTCGGCCTACTGAGTAGCTGGGACTACAAGCGCCTG T C EIF2AK2 Ensembl:ENSG00000055332 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1357962910 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48602,RMVar_hsa_circ_13772,RMVar_hsa_circ_341163,RMVar_hsa_circ_32277,RMVar_hsa_circ_122724,RMVar_hsa_circ_93727,RMVar_hsa_circ_198955,RMVar_hsa_circ_49371,RMVar_hsa_circ_198956,RMVar_hsa_circ_6737 19022 RMVar_ID_19022 Human_SNP_ID_67448862 A-to-I Human chr2 - 37142269 37142269 37142269 AAAATTACCCAGGCATGGTGGTGTGTGCCTGTAGTTCCAGGTGCTTGTGAGGCTGAGACAGGAAG AAAATTACCCAGGCATGGTGGTGTGTGCCTGTTGTTCCAGGTGCTTGTGAGGCTGAGACAGGAAG T A EIF2AK2 Ensembl:ENSG00000055332 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs184062730 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48602,RMVar_hsa_circ_13772,RMVar_hsa_circ_341163,RMVar_hsa_circ_32277,RMVar_hsa_circ_122724,RMVar_hsa_circ_93727,RMVar_hsa_circ_198955,RMVar_hsa_circ_49371,RMVar_hsa_circ_198956,RMVar_hsa_circ_365805 19023 RMVar_ID_19023 Human_SNP_ID_67448863 A-to-I Human chr2 - 37142269 37142269 37142269 AAAATTACCCAGGCATGGTGGTGTGTGCCTGTAGTTCCAGGTGCTTGTGAGGCTGAGACAGGAAG AAAATTACCCAGGCATGGTGGTGTGTGCCTGTGGTTCCAGGTGCTTGTGAGGCTGAGACAGGAAG T C EIF2AK2 Ensembl:ENSG00000055332 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs184062730 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48602,RMVar_hsa_circ_13772,RMVar_hsa_circ_341163,RMVar_hsa_circ_32277,RMVar_hsa_circ_122724,RMVar_hsa_circ_93727,RMVar_hsa_circ_198955,RMVar_hsa_circ_49371,RMVar_hsa_circ_198956,RMVar_hsa_circ_365805 19024 RMVar_ID_19024 Human_SNP_ID_67449084 A-to-I Human chr2 - 37143105 37143105 37143105 TCTGCCTCAGCCTCCTGAGTAGCTGAGATTACAGGCACCCACCACCACGGCCAGCTAATTTTTTG TCTGCCTCAGCCTCCTGAGTAGCTGAGATTACCGGCACCCACCACCACGGCCAGCTAATTTTTTG T G EIF2AK2 Ensembl:ENSG00000055332 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs557069754 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48602,RMVar_hsa_circ_13772,RMVar_hsa_circ_341163,RMVar_hsa_circ_32277,RMVar_hsa_circ_122724,RMVar_hsa_circ_93727,RMVar_hsa_circ_198955,RMVar_hsa_circ_49371,RMVar_hsa_circ_198956,RMVar_hsa_circ_365805 19025 RMVar_ID_19025 Human_SNP_ID_67449613 A-to-I Human chr2 - 37144828 37144828 37144828 CCTGTAGTCCCAGCACTTTGGTAGGTCAAGGTAGGTGGATCACTTGAATTTGGGAGTTTGAGATT CCTGTAGTCCCAGCACTTTGGTAGGTCAAGGTCGGTGGATCACTTGAATTTGGGAGTTTGAGATT T G EIF2AK2 Ensembl:ENSG00000055332 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1049025525 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48602,RMVar_hsa_circ_13772,RMVar_hsa_circ_341163,RMVar_hsa_circ_32277,RMVar_hsa_circ_122724,RMVar_hsa_circ_93727,RMVar_hsa_circ_198955,RMVar_hsa_circ_49371,RMVar_hsa_circ_198956,RMVar_hsa_circ_365805 19026 RMVar_ID_19026 Human_SNP_ID_67451800 A-to-I Human chr2 - 37152344 37152344 37152344 CTGGGAGGCAGATGCTGCAGTGAGCTGAGATCATGTTACTGCACTCCAGCCTGGGCAACAGAGTG CTGGGAGGCAGATGCTGCAGTGAGCTGAGATCCTGTTACTGCACTCCAGCCTGGGCAACAGAGTG T G EIF2AK2 Ensembl:ENSG00000055332 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1394497860 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9983361 19027 RMVar_ID_19027 Human_SNP_ID_67451830 A-to-I Human chr2 - 37152454 37152454 37152454 CAACACCGGGAAACCTCAAAAATACAAAAATTAGCTGGGCGTGGTGGTGGGCACCTGTAGTCCCA CAACACCGGGAAACCTCAAAAATACAAAAATTGGCTGGGCGTGGTGGTGGGCACCTGTAGTCCCA T C EIF2AK2 Ensembl:ENSG00000055332 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs968124132 Functional Loss SNV dbSNP153 33..33 33 - - - 19028 RMVar_ID_19028 Human_SNP_ID_67452123 A-to-I Human chr2 - 37153414 37153414 37153414 GATCGCTTGAGCCCAGAGTTCAAGGCTGCAGTAAGCTGTGATCACACCACTGCACTCCAGCCTGG GATCGCTTGAGCCCAGAGTTCAAGGCTGCAGTGAGCTGTGATCACACCACTGCACTCCAGCCTGG T C EIF2AK2 Ensembl:ENSG00000055332 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1038731015 Functional Loss SNV dbSNP153 33..33 33 - - - 19029 RMVar_ID_19029 Human_SNP_ID_67452825 A-to-I Human chr2 - 37155793 37155793 37155793 GGGACTACAGGTGCCCGCCAGCACAGCCAACTAATTTTTTTATTTTTAGTAGAGACAGGGTTTCA GGGACTACAGGTGCCCGCCAGCACAGCCAACTGATTTTTTTATTTTTAGTAGAGACAGGGTTTCA T C EIF2AK2 Ensembl:ENSG00000055332 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs951167034 Functional Loss SNV dbSNP153 33..33 33 - - - 19030 RMVar_ID_19030 Human_SNP_ID_67452826 A-to-I Human chr2 - 37155793 37155793 37155793 GGGACTACAGGTGCCCGCCAGCACAGCCAACTAATTTTTTTATTTTTAGTAGAGACAGGGTTTCA GGGACTACAGGTGCCCGCCAGCACAGCCAACTCATTTTTTTATTTTTAGTAGAGACAGGGTTTCA T G EIF2AK2 Ensembl:ENSG00000055332 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs951167034 Functional Loss SNV dbSNP153 33..33 33 - - - 19031 RMVar_ID_19031 Human_SNP_ID_67452827 A-to-I Human chr2 - 37155796 37155796 37155796 GCTGGGACTACAGGTGCCCGCCAGCACAGCCAACTAATTTTTTTATTTTTAGTAGAGACAGGGTT GCTGGGACTACAGGTGCCCGCCAGCACAGCCAGCTAATTTTTTTATTTTTAGTAGAGACAGGGTT T C EIF2AK2 Ensembl:ENSG00000055332 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs758165148 Functional Loss SNV dbSNP153 33..33 33 - - - 19032 RMVar_ID_19032 Human_SNP_ID_67452851 A-to-I Human chr2 - 37155858 37155858 37155858 GGGCTCACTGCAACCTCTGCCTCTCAGGTTCAAGCGATTTTCCTTCCTCAGCCTCCCAGGTAGCT GGGCTCACTGCAACCTCTGCCTCTCAGGTTCAGGCGATTTTCCTTCCTCAGCCTCCCAGGTAGCT T C EIF2AK2 Ensembl:ENSG00000055332 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1424669393 Functional Loss SNV dbSNP153 33..33 33 - - - 19033 RMVar_ID_19033 Human_SNP_ID_67467932 A-to-I Human chr2 + 37202383 37202383 37202383 AATATTCCTATCAGCCAGGCATGGTGGCTCACACCAGTAATCTCAGCACTTTGGGAGGCCGAGGC AATATTCCTATCAGCCAGGCATGGTGGCTCACGCCAGTAATCTCAGCACTTTGGGAGGCCGAGGC A G CEBPZOS Ensembl:ENSG00000218739 Protein coding intron GSE38233;GSE100210;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 24183664,29129909,30559470 RNA-Seq:(High) rs1027287463 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_550354,Human_RBP_ID_26482592 Human_miRNA_ID_56872,Human_miRNA_ID_1111573,Human_miRNA_ID_1637901,Human_miRNA_ID_1941155,Human_miRNA_ID_1944212,Human_miRNA_ID_2115346,Human_miRNA_ID_2198920,Human_miRNA_ID_2201989,Human_miRNA_ID_2314414,Human_miRNA_ID_2317576,Human_miRNA_ID_2320730,Human_miRNA_ID_2323884,Human_miRNA_ID_2518264,Human_miRNA_ID_2521438,Human_miRNA_ID_2773328,Human_miRNA_ID_2814454,Human_miRNA_ID_2820630,Human_miRNA_ID_2826766,Human_miRNA_ID_2829916,Human_miRNA_ID_2834036,Human_miRNA_ID_2839405,Human_miRNA_ID_2844571,Human_miRNA_ID_2847592,Human_miRNA_ID_2861713,Human_miRNA_ID_3111440 RMVar_hsa_circ_115798,RMVar_hsa_circ_322185,RMVar_hsa_circ_198959,RMVar_hsa_circ_198961,RMVar_hsa_circ_98273 19034 RMVar_ID_19034 Human_SNP_ID_67467986 A-to-I Human chr2 + 37202546 37202546 37202546 GCATGCCTGTAATCCCAGCTACTTGGGAGGCTAAGGTAGGAGAATTACTTGAACATGGGAGATGG GCATGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGTAGGAGAATTACTTGAACATGGGAGATGG A G CEBPZOS Ensembl:ENSG00000218739 Protein coding intron GSE47997;GSE38233;GSE100210;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;HepG2 cell line - 23474544,24183664,29129909,29129909 RNA-Seq:(High) rs567883929 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569522,Human_RBP_ID_26486343 Human_miRNA_ID_2281027,Human_miRNA_ID_2282591,Human_miRNA_ID_2630637 RMVar_hsa_circ_115798,RMVar_hsa_circ_322185,RMVar_hsa_circ_198959,RMVar_hsa_circ_198961,RMVar_hsa_circ_98273 19035 RMVar_ID_19035 Human_SNP_ID_67467992 A-to-I Human chr2 + 37202590 37202590 37202590 TTACTTGAACATGGGAGATGGAGGTTGCAGTGAGCCAAGATCATGCCACTGCATTCCAACCTGGG TTACTTGAACATGGGAGATGGAGGTTGCAGTGGGCCAAGATCATGCCACTGCATTCCAACCTGGG A G CEBPZOS Ensembl:ENSG00000218739 Protein coding intron GSE47997;GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,29129909,31158229,31158229,32596459,32596459 RNA-Seq:(High) rs1341654662 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569522,Human_RBP_ID_26486343 RMVar_hsa_circ_115798,RMVar_hsa_circ_322185,RMVar_hsa_circ_198959,RMVar_hsa_circ_198961,RMVar_hsa_circ_98273 19036 RMVar_ID_19036 Human_SNP_ID_67468003 A-to-I Human chr2 + 37202615 37202614 37202615 TGCAGTGAGCCAAGATCATGCCACTGCATTCCAACCTGGGCAAGGGAGTGAGACGCTGTCTCAAA TGCAGTGAGCCAAGATCATGCCACTGCATTCC_ACCTGGGCAAGGGAGTGAGACGCTGTCTCAAA CA C CEBPZOS Ensembl:ENSG00000218739 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1385442740 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_1241132,Human_RBP_ID_6916210,Human_RBP_ID_25538623 RMVar_hsa_circ_115798,RMVar_hsa_circ_322185,RMVar_hsa_circ_198959,RMVar_hsa_circ_198961,RMVar_hsa_circ_98273 19037 RMVar_ID_19037 Human_SNP_ID_67468004 A-to-I Human chr2 + 37202615 37202615 37202615 TGCAGTGAGCCAAGATCATGCCACTGCATTCCAACCTGGGCAAGGGAGTGAGACGCTGTCTCAAA TGCAGTGAGCCAAGATCATGCCACTGCATTCCCACCTGGGCAAGGGAGTGAGACGCTGTCTCAAA A C CEBPZOS Ensembl:ENSG00000218739 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1337760070 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1241132,Human_RBP_ID_6916210,Human_RBP_ID_25538623 RMVar_hsa_circ_115798,RMVar_hsa_circ_322185,RMVar_hsa_circ_198959,RMVar_hsa_circ_198961,RMVar_hsa_circ_98273 19038 RMVar_ID_19038 Human_SNP_ID_67468008 A-to-I Human chr2 + 37202624 37202624 37202624 CCAAGATCATGCCACTGCATTCCAACCTGGGCAAGGGAGTGAGACGCTGTCTCAAAAAAAAAAAA CCAAGATCATGCCACTGCATTCCAACCTGGGCGAGGGAGTGAGACGCTGTCTCAAAAAAAAAAAA A G CEBPZOS Ensembl:ENSG00000218739 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1463574978 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1241133,Human_RBP_ID_4608398,Human_RBP_ID_6916210,Human_RBP_ID_22992429,Human_RBP_ID_25538623 RMVar_hsa_circ_115798,RMVar_hsa_circ_322185,RMVar_hsa_circ_198959,RMVar_hsa_circ_198961,RMVar_hsa_circ_98273 19039 RMVar_ID_19039 Human_SNP_ID_67468010 A-to-I Human chr2 + 37202633 37202633 37202633 TGCCACTGCATTCCAACCTGGGCAAGGGAGTGAGACGCTGTCTCAAAAAAAAAAAAAAAAAAAAA TGCCACTGCATTCCAACCTGGGCAAGGGAGTGGGACGCTGTCTCAAAAAAAAAAAAAAAAAAAAA A G CEBPZOS Ensembl:ENSG00000218739 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs763826785 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1241133,Human_RBP_ID_22992429,Human_RBP_ID_25538623 RMVar_hsa_circ_115798,RMVar_hsa_circ_322185,RMVar_hsa_circ_198959,RMVar_hsa_circ_198961,RMVar_hsa_circ_98273 19040 RMVar_ID_19040 Human_SNP_ID_67468626 A-to-I Human chr2 + 37204298 37204298 37204298 GCTAATTTTTGATTTTTTTTTTTTTTTTTTTGAGACAGAGTCTCGCTTTGTCGCCAGGCTGGAGT GCTAATTTTTGATTTTTTTTTTTTTTTTTTTGTGACAGAGTCTCGCTTTGTCGCCAGGCTGGAGT A T CEBPZOS Ensembl:ENSG00000218739 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1260176398 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26486352 RMVar_hsa_circ_115798,RMVar_hsa_circ_322185,RMVar_hsa_circ_198959,RMVar_hsa_circ_198961,RMVar_hsa_circ_98273 19041 RMVar_ID_19041 Human_SNP_ID_67468678 A-to-I Human chr2 + 37204443 37204443 37204443 GGGCCTACAAGTGCATGCCACCACGCCAAGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCA GGGCCTACAAGTGCATGCCACCACGCCAAGCTGATTTTTGTATTTTTAGTAGAGATGGGGTTTCA A G CEBPZOS Ensembl:ENSG00000218739 Protein coding intron GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-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 19042 RMVar_ID_19042 Human_SNP_ID_67468700 A-to-I Human chr2 + 37204507 37204507 37204507 ATCATGTTGGCCAGGATGGTCTTGATCTCTTGACCTTGTGATCTACCTGCCTTGGCCTCCCAAAG ATCATGTTGGCCAGGATGGTCTTGATCTCTTGCCCTTGTGATCTACCTGCCTTGGCCTCCCAAAG A C CEBPZOS Ensembl:ENSG00000218739 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1416780930 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2778926,Human_miRNA_ID_2941541 RMVar_hsa_circ_115798,RMVar_hsa_circ_322185,RMVar_hsa_circ_198959,RMVar_hsa_circ_198961,RMVar_hsa_circ_98273 19043 RMVar_ID_19043 Human_SNP_ID_67477858 A-to-I Human chr2 + 37234251 37234251 37234251 AGTTGGGATTACAGGTGTATGTTTCCATGCCCAGCTAGGTTTTTTGTATTTTCAATGGAGATCGG AGTTGGGATTACAGGTGTATGTTTCCATGCCCCGCTAGGTTTTTTGTATTTTCAATGGAGATCGG A C NDUFAF7 Ensembl:ENSG00000003509 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1238467224 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60374,RMVar_hsa_circ_378715 19044 RMVar_ID_19044 Human_SNP_ID_67479455 A-to-I Human chr2 + 37239539 37239539 37239539 GATATACCCTAGAGAAACTAGTGTATATGTGTACCAGGAGACACATACAAGAAGATAGCAGCATT GATATACCCTAGAGAAACTAGTGTATATGTGTGCCAGGAGACACATACAAGAAGATAGCAGCATT A G NDUFAF7 Ensembl:ENSG00000003509 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11124569 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_1630,GWAS_ID_1631,GWAS_ID_1632,GWAS_ID_1633,GWAS_ID_1634,GWAS_ID_1635,GWAS_ID_1636,GWAS_ID_1637,GWAS_ID_1638,GWAS_ID_1639,GWAS_ID_1640,GWAS_ID_1641,GWAS_ID_1642,GWAS_ID_1643,GWAS_ID_1644,GWAS_ID_1645,GWAS_ID_1646,GWAS_ID_1647,GWAS_ID_1648,GWAS_ID_1649,GWAS_ID_1650,GWAS_ID_1651,GWAS_ID_1652,GWAS_ID_1653,GWAS_ID_1654,GWAS_ID_1655,GWAS_ID_1656,GWAS_ID_1657,GWAS_ID_1658,GWAS_ID_1659 RMVar_hsa_circ_107491,RMVar_hsa_circ_301687,RMVar_hsa_circ_198967,RMVar_hsa_circ_198968,RMVar_hsa_circ_198969,RMVar_hsa_circ_286444 19045 RMVar_ID_19045 Human_SNP_ID_67649091 A-to-I Human chr2 - 37817177 37817177 37817177 ATTTATGAGCCAAGGTCATCAATTCATCTCCTAAGACAGCATCCCACACTTTGGCTGTGAAATCT ATTTATGAGCCAAGGTCATCAATTCATCTCCTGAGACAGCATCCCACACTTTGGCTGTGAAATCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1370674772 Functional Loss SNV dbSNP153 33..33 33 - - - 19046 RMVar_ID_19046 Human_SNP_ID_67649114 A-to-I Human chr2 - 37817234 37817234 37817234 GTCCCTTGGTTAACAAATAATTACTATCCTGCATGAAATACACAGTCTTGACAATGTATTTATGA GTCCCTTGGTTAACAAATAATTACTATCCTGCGTGAAATACACAGTCTTGACAATGTATTTATGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1228703291 Functional Loss SNV dbSNP153 33..33 33 - - - 19047 RMVar_ID_19047 Human_SNP_ID_67649143 A-to-I Human chr2 + 37817305 37817305 37817305 AACTGTTACGCATGTATGACTTGAACAAACCCAAAGCAAGACCTAAGGAAATTAGTGGTCACACT AACTGTTACGCATGTATGACTTGAACAAACCCGAAGCAAGACCTAAGGAAATTAGTGGTCACACT A G AC010878.1 Ensembl:ENSG00000225402 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444518356 Functional Loss SNV dbSNP153 33..33 33 - - - 19048 RMVar_ID_19048 Human_SNP_ID_67736883 A-to-I Human chr2 - 38111677 38111676 38111677 AGGATTATAAATCATTCTACTATAATGACACAAGGACATGTATGTTTGTTGCAGCACTATTTACA AGGATTATAAATCATTCTACTATAATGACACA_GGACATGTATGTTTGTTGCAGCACTATTTACA CT C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1283344933 Functional Loss DEL dbSNP153 33..33 33 - - - 19049 RMVar_ID_19049 Human_SNP_ID_67742870 A-to-I Human chr2 - 38130777 38130777 38130777 ATAAATGATACTAGTACAGTAAGTCCTCACTTAATGTCATCGATAGGTTCTTGGAATCTGTAACT ATAAATGATACTAGTACAGTAAGTCCTCACTTGATGTCATCGATAGGTTCTTGGAATCTGTAACT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1181865905 Functional Loss SNV dbSNP153 33..33 33 - - - 19050 RMVar_ID_19050 Human_SNP_ID_67752834 A-to-I Human chr2 - 38161423 38161423 38161423 TTGCTCCTTTCTCTTCTCCAGACACAATTTCAATTCCCAGAATGTCGATCTCAATCCACTGAGGA TTGCTCCTTTCTCTTCTCCAGACACAATTTCAGTTCCCAGAATGTCGATCTCAATCCACTGAGGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1393227913 Functional Loss SNV dbSNP153 33..33 33 - - - 19051 RMVar_ID_19051 Human_SNP_ID_67752835 A-to-I Human chr2 - 38161423 38161423 38161423 TTGCTCCTTTCTCTTCTCCAGACACAATTTCAATTCCCAGAATGTCGATCTCAATCCACTGAGGA TTGCTCCTTTCTCTTCTCCAGACACAATTTCACTTCCCAGAATGTCGATCTCAATCCACTGAGGA T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1393227913 Functional Loss SNV dbSNP153 33..33 33 - - - 19052 RMVar_ID_19052 Human_SNP_ID_67753289 A-to-I Human chr2 - 38162888 38162888 38162888 AGCTCTGTGTTTAAAAAGAGTTGCTTTACATTAGAACATAATATTCTTAGCAGATTGAGATCAAC AGCTCTGTGTTTAAAAAGAGTTGCTTTACATTTGAACATAATATTCTTAGCAGATTGAGATCAAC T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1307171183 Functional Loss SNV dbSNP153 33..33 33 - - - 19053 RMVar_ID_19053 Human_SNP_ID_67762372 A-to-I Human chr2 - 38195537 38195537 38195537 GTCAGGCTGGTCTCAATCTCCTGACCTCAGGTAATCTGCCCGCCTTGGCCTCCCAAAGTGTAGGG GTCAGGCTGGTCTCAATCTCCTGACCTCAGGTCATCTGCCCGCCTTGGCCTCCCAAAGTGTAGGG T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1261827749 Functional Loss SNV dbSNP153 33..33 33 - - - 19054 RMVar_ID_19054 Human_SNP_ID_67807958 A-to-I Human chr2 - 38339159 38339159 38339159 CAGGCTGGAGTGCAGTAGCGCAGTCTCGGCTCACTGCAACCTCCGCCTCCTGAGTTCAAGCGATT CAGGCTGGAGTGCAGTAGCGCAGTCTCGGCTCTCTGCAACCTCCGCCTCCTGAGTTCAAGCGATT T A ATL2 Ensembl:ENSG00000119787 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs944321183 Functional Loss SNV dbSNP153 33..33 33 - - - 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 19055 RMVar_ID_19055 Human_SNP_ID_67809259 A-to-I Human chr2 - 38343032 38343032 38343032 GCAATCCTCCCACCTCAGCCTCCCGAGAAGCTAGGACTACAGGCGTGTGCCACCATGCCCAACTC GCAATCCTCCCACCTCAGCCTCCCGAGAAGCTGGGACTACAGGCGTGTGCCACCATGCCCAACTC T C ATL2 Ensembl:ENSG00000119787 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1134744 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13877647 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 19056 RMVar_ID_19056 Human_SNP_ID_67811010 A-to-I Human chr2 - 38348383 38348383 38348383 TGGCTCACCGCAACCTCCGTTTCCTGGGTTCAAGCAATTCTCCTCCCTCAGCCTCCTGAGTATCT TGGCTCACCGCAACCTCCGTTTCCTGGGTTCAGGCAATTCTCCTCCCTCAGCCTCCTGAGTATCT T C ATL2 Ensembl:ENSG00000119787 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1156519156 Functional Loss SNV dbSNP153 33..33 33 - - - 19057 RMVar_ID_19057 Human_SNP_ID_67813657 A-to-I Human chr2 - 38356322 38356322 38356322 AAATTAGCTGGCTCACGCTTGTAGTCCCAACTACTTGGGAGGCTGAGGGAGGAGAATTGCTTGAG AAATTAGCTGGCTCACGCTTGTAGTCCCAACTGCTTGGGAGGCTGAGGGAGGAGAATTGCTTGAG T C ATL2 Ensembl:ENSG00000119787 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs753564160 Functional Loss SNV dbSNP153 33..33 33 - - - 19058 RMVar_ID_19058 Human_SNP_ID_67871104 A-to-I Human chr2 - 38546033 38546033 38546033 AGTGCAGTACAGCATAATCTCGGCTCACTGCAACCTCTGCCTCCTGGGCTCAAGGGATTCTTGTG AGTGCAGTACAGCATAATCTCGGCTCACTGCATCCTCTGCCTCCTGGGCTCAAGGGATTCTTGTG T A lnc-HNRNPLL-1 RNACentral:URS0000EBA37D lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1186635907 Functional Loss SNV dbSNP153 33..33 33 - - - 19059 RMVar_ID_19059 Human_SNP_ID_67876984 A-to-I Human chr2 - 38566311 38566311 38566311 CAGACTGTAGAGTAGTGGCACGATCTTGGCTCACTGCAACCTCCACCTCCCAGGTTCAAGCGATT CAGACTGTAGAGTAGTGGCACGATCTTGGCTCGCTGCAACCTCCACCTCCCAGGTTCAAGCGATT T C HNRNPLL Ensembl:ENSG00000143889 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355899847 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13878490 19060 RMVar_ID_19060 Human_SNP_ID_67887933 A-to-I Human chr2 - 38602832 38602832 38602832 TTGGCTCGGTAATTGAGAGGAGCGGCCGCTCCAGAGCTTCCTCCCGGGGCGCCCCCCTCAGTCCG TTGGCTCGGTAATTGAGAGGAGCGGCCGCTCCGGAGCTTCCTCCCGGGGCGCCCCCCTCAGTCCG T C HNRNPLL Ensembl:ENSG00000143889 Protein coding 5'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs556524230 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_777832,Human_RBP_ID_1067898,Human_RBP_ID_4624226,Human_RBP_ID_9297132,Human_RBP_ID_9330422,Human_RBP_ID_18421743,Human_RBP_ID_26338520 19061 RMVar_ID_19061 Human_SNP_ID_67887934 A-to-I Human chr2 - 38602832 38602832 38602832 TTGGCTCGGTAATTGAGAGGAGCGGCCGCTCCAGAGCTTCCTCCCGGGGCGCCCCCCTCAGTCCG TTGGCTCGGTAATTGAGAGGAGCGGCCGCTCCCGAGCTTCCTCCCGGGGCGCCCCCCTCAGTCCG T G HNRNPLL Ensembl:ENSG00000143889 Protein coding 5'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs556524230 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_777832,Human_RBP_ID_1067898,Human_RBP_ID_4624226,Human_RBP_ID_9297132,Human_RBP_ID_9330422,Human_RBP_ID_18421743,Human_RBP_ID_26338520 19062 RMVar_ID_19062 Human_SNP_ID_67911982 A-to-I Human chr2 + 38683828 38683828 38683828 ACCTCGGGTGATCCACCCGCTTCAGCCTCCCAAAGTGCTAGGATTACAGGCGTGAGCCACCGCAC ACCTCGGGTGATCCACCCGCTTCAGCCTCCCAGAGTGCTAGGATTACAGGCGTGAGCCACCGCAC A G GALM Ensembl:ENSG00000143891 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs932600463 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_199034,RMVar_hsa_circ_353426,RMVar_hsa_circ_347579 19063 RMVar_ID_19063 Human_SNP_ID_67914933 A-to-I Human chr2 + 38694088 38694088 38694088 CCTGTGGTCCCAGCTATTTGGGAGGCTGAGGTAAGACAATTGCTTGAGCCCAGGAGGTCAAGGCT CCTGTGGTCCCAGCTATTTGGGAGGCTGAGGTTAGACAATTGCTTGAGCCCAGGAGGTCAAGGCT A T GALM Ensembl:ENSG00000143891 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1488941661 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_347579 19064 RMVar_ID_19064 Human_SNP_ID_67915446 A-to-I Human chr2 - 38695872 38695872 38695872 CAACATGGTGAAACCCCATTTCTACTAAAAATACAAAAATTATCCGGGTATGGTGGCATGCGCGC CAACATGGTGAAACCCCATTTCTACTAAAAATCCAAAAATTATCCGGGTATGGTGGCATGCGCGC T G HSALNG0014329 RNACentral:URS0000E96D22 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs564960851 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_199035 19065 RMVar_ID_19065 Human_SNP_ID_67917780 A-to-I Human chr2 + 38704436 38704435 38704436 TCATGCCTTTAATCCCAGAACTTTGAGAGGCTAAGGCGGGAGGATTGATTGGGTCCAGGAGTTCA TCATGCCTTTAATCCCAGAACTTTGAGAGGCT_AGGCGGGAGGATTGATTGGGTCCAGGAGTTCA TA T GALM Ensembl:ENSG00000143891 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs534365136 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_17569528 19066 RMVar_ID_19066 Human_SNP_ID_67942553 A-to-I Human chr2 + 38779944 38779944 38779944 ACCTCAGGTGATCTGCCCACCTTGGCCTCCCAAAGTGCTAGGATCATAGGCTTGAGCCACCGTCC ACCTCAGGTGATCTGCCCACCTTGGCCTCCCACAGTGCTAGGATCATAGGCTTGAGCCACCGTCC A C GEMIN6 Ensembl:ENSG00000152147 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1272074935 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_199046,RMVar_hsa_circ_101692 19067 RMVar_ID_19067 Human_SNP_ID_67942554 A-to-I Human chr2 + 38779944 38779944 38779944 ACCTCAGGTGATCTGCCCACCTTGGCCTCCCAAAGTGCTAGGATCATAGGCTTGAGCCACCGTCC ACCTCAGGTGATCTGCCCACCTTGGCCTCCCAGAGTGCTAGGATCATAGGCTTGAGCCACCGTCC A G GEMIN6 Ensembl:ENSG00000152147 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1272074935 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_199046,RMVar_hsa_circ_101692 19068 RMVar_ID_19068 Human_SNP_ID_67942858 A-to-I Human chr2 + 38780801 38780801 38780801 TAGACATGTGCTACCACACCCGGCTAATTTTTATATTTTTAGTAGAGATGGGGTTTCACCATGTT TAGACATGTGCTACCACACCCGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTT A G GEMIN6 Ensembl:ENSG00000152147 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs3112202 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_199046,RMVar_hsa_circ_101692 19069 RMVar_ID_19069 Human_SNP_ID_67944073 A-to-I Human chr2 + 38784277 38784275 38784277 AAAAGGAAGAAGCCAGCTGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCTAG AAAAGGAAGAAGCCAGCTGGGCGCGGTGGCT__CGCCTGTAATCCCAGCACTTTGGGAGGCCTAG TCA T GEMIN6 Ensembl:ENSG00000152147 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1356370464 Functional Loss DEL dbSNP153 32..33 33 - - - 19070 RMVar_ID_19070 Human_SNP_ID_67952615 A-to-I Human chr2 + 38811319 38811318 38811319 GCTCAAACCAGACCTGATCGTTCCCCTTTCCCATGGCACTGTGGGACACATACTTTGCCCCCTCC GCTCAAACCAGACCTGATCGTTCCCCTTTCCC_TGGCACTGTGGGACACATACTTTGCCCCCTCC CA C lnc-GEMIN6-1,lnc-GEMIN6-1:2,lnc-GEMIN6-1:3 RNACentral:URS00008BDA9B,RNACentral:URS00008BAAF7,RNACentral:URS00008B6341 lincRNA,lincRNA,lincRNA intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs979456832 Functional Loss DEL dbSNP153 33..33 33 - - - 19071 RMVar_ID_19071 Human_SNP_ID_67952616 A-to-I Human chr2 + 38811319 38811319 38811319 GCTCAAACCAGACCTGATCGTTCCCCTTTCCCATGGCACTGTGGGACACATACTTTGCCCCCTCC GCTCAAACCAGACCTGATCGTTCCCCTTTCCCGTGGCACTGTGGGACACATACTTTGCCCCCTCC A G lnc-GEMIN6-1,lnc-GEMIN6-1:2,lnc-GEMIN6-1:3 RNACentral:URS00008BDA9B,RNACentral:URS00008BAAF7,RNACentral:URS00008B6341 lincRNA,lincRNA,lincRNA intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1382385721 Functional Loss SNV dbSNP153 33..33 33 - - - 19072 RMVar_ID_19072 Human_SNP_ID_67952619 A-to-I Human chr2 + 38811324 38811324 38811324 AACCAGACCTGATCGTTCCCCTTTCCCATGGCACTGTGGGACACATACTTTGCCCCCTCCCACTG AACCAGACCTGATCGTTCCCCTTTCCCATGGCGCTGTGGGACACATACTTTGCCCCCTCCCACTG A G lnc-GEMIN6-1,lnc-GEMIN6-1:2,lnc-GEMIN6-1:3 RNACentral:URS00008BDA9B,RNACentral:URS00008BAAF7,RNACentral:URS00008B6341 lincRNA,lincRNA,lincRNA intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs761830386 Functional Loss SNV dbSNP153 33..33 33 - - - 19073 RMVar_ID_19073 Human_SNP_ID_68003391 A-to-I Human chr2 - 38993001 38993001 38993001 AAACTTCTGGCCTCAAACAAACCTCCTGCCTTAACCTTCCAAAGTGCTGGGGTTATAGATGAGCC AAACTTCTGGCCTCAAACAAACCTCCTGCCTTTACCTTCCAAAGTGCTGGGGTTATAGATGAGCC T A SOS1,SOS1-IT1 Ensembl:ENSG00000115904,Ensembl:ENSG00000229692 Protein coding,lincRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941944322 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_550824,Human_RBP_ID_17569530,Human_RBP_ID_25540587 Human_Splice_Rec_237958,Human_Splice_Rec_237960 RMVar_hsa_circ_64687,RMVar_hsa_circ_104583,RMVar_hsa_circ_199077 19074 RMVar_ID_19074 Human_SNP_ID_68032166 A-to-I Human chr2 - 39097696 39097696 39097696 AGCTGGGCATGATGGTGCATGCCTGTAATCCCAGCTACTGGGGAGGCTGGGATGGGAGAATCACT AGCTGGGCATGATGGTGCATGCCTGTAATCCCTGCTACTGGGGAGGCTGGGATGGGAGAATCACT T A SOS1 Ensembl:ENSG00000115904 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs185093451 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569535 RMVar_hsa_circ_117146,RMVar_hsa_circ_199095,RMVar_hsa_circ_199101 19075 RMVar_ID_19075 Human_SNP_ID_68038086 A-to-I Human chr2 - 39116635 39116635 39116635 GAACTCCTGGGCTCAAGCCATCTGCCTGCCTCAGCTTCCCAAAGTGCTAGGATTACAGGGTGAGC GAACTCCTGGGCTCAAGCCATCTGCCTGCCTCGGCTTCCCAAAGTGCTAGGATTACAGGGTGAGC T C SOS1 Ensembl:ENSG00000115904 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs888381860 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22721932,Human_RBP_ID_25588921 RMVar_hsa_circ_117146,RMVar_hsa_circ_199095 19076 RMVar_ID_19076 Human_SNP_ID_68082664 A-to-I Human chr2 - 39275430 39275430 39275430 TCACCCAGGCTGGAGGGCAGTGGCGTGAACACAGCTCACTGCAGCCTTGACCTCCTGGGCTCAAG TCACCCAGGCTGGAGGGCAGTGGCGTGAACACGGCTCACTGCAGCCTTGACCTCCTGGGCTCAAG T C MAP4K3 Ensembl:ENSG00000011566 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1286169419 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2324,RMVar_hsa_circ_81793,RMVar_hsa_circ_103557,RMVar_hsa_circ_199113,RMVar_hsa_circ_199114,RMVar_hsa_circ_127067,RMVar_hsa_circ_31511,RMVar_hsa_circ_83400,RMVar_hsa_circ_336403,RMVar_hsa_circ_199115,RMVar_hsa_circ_119828,RMVar_hsa_circ_35725,RMVar_hsa_circ_199116,RMVar_hsa_circ_199117,RMVar_hsa_circ_199118,RMVar_hsa_circ_349605,RMVar_hsa_circ_351418,RMVar_hsa_circ_310367,RMVar_hsa_circ_282430,RMVar_hsa_circ_50437,RMVar_hsa_circ_17038,RMVar_hsa_circ_199122,RMVar_hsa_circ_199123,RMVar_hsa_circ_199125,RMVar_hsa_circ_6619,RMVar_hsa_circ_19474,RMVar_hsa_circ_297253,RMVar_hsa_circ_318036,RMVar_hsa_circ_319562,RMVar_hsa_circ_107444,RMVar_hsa_circ_330081,RMVar_hsa_circ_362146,RMVar_hsa_circ_199124,RMVar_hsa_circ_351276,RMVar_hsa_circ_303416,RMVar_hsa_circ_70685,RMVar_hsa_circ_92589,RMVar_hsa_circ_34904,RMVar_hsa_circ_290890,RMVar_hsa_circ_199126,RMVar_hsa_circ_199128,RMVar_hsa_circ_39648,RMVar_hsa_circ_199127,RMVar_hsa_circ_331314,RMVar_hsa_circ_352524,RMVar_hsa_circ_345172,RMVar_hsa_circ_300519,RMVar_hsa_circ_272046,RMVar_hsa_circ_275649,RMVar_hsa_circ_72099,RMVar_hsa_circ_199131,RMVar_hsa_circ_199133,RMVar_hsa_circ_199134,RMVar_hsa_circ_199132,RMVar_hsa_circ_199130,RMVar_hsa_circ_199135 19077 RMVar_ID_19077 Human_SNP_ID_68082806 A-to-I Human chr2 - 39275997 39275997 39275997 ATGGTCATGTGCAGCTGTAGTCCCAGCTACTCAGGAGGCTGAGACAGGAGAATCACTTAAACCCG ATGGTCATGTGCAGCTGTAGTCCCAGCTACTCGGGAGGCTGAGACAGGAGAATCACTTAAACCCG T C MAP4K3 Ensembl:ENSG00000011566 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs919423416 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569546 RMVar_hsa_circ_2324,RMVar_hsa_circ_81793,RMVar_hsa_circ_103557,RMVar_hsa_circ_199113,RMVar_hsa_circ_199114,RMVar_hsa_circ_127067,RMVar_hsa_circ_31511,RMVar_hsa_circ_83400,RMVar_hsa_circ_336403,RMVar_hsa_circ_199115,RMVar_hsa_circ_119828,RMVar_hsa_circ_35725,RMVar_hsa_circ_199116,RMVar_hsa_circ_199117,RMVar_hsa_circ_199118,RMVar_hsa_circ_349605,RMVar_hsa_circ_351418,RMVar_hsa_circ_310367,RMVar_hsa_circ_282430,RMVar_hsa_circ_50437,RMVar_hsa_circ_17038,RMVar_hsa_circ_199122,RMVar_hsa_circ_199123,RMVar_hsa_circ_199125,RMVar_hsa_circ_6619,RMVar_hsa_circ_19474,RMVar_hsa_circ_297253,RMVar_hsa_circ_318036,RMVar_hsa_circ_319562,RMVar_hsa_circ_107444,RMVar_hsa_circ_330081,RMVar_hsa_circ_362146,RMVar_hsa_circ_199124,RMVar_hsa_circ_351276,RMVar_hsa_circ_303416,RMVar_hsa_circ_70685,RMVar_hsa_circ_92589,RMVar_hsa_circ_34904,RMVar_hsa_circ_290890,RMVar_hsa_circ_199126,RMVar_hsa_circ_199128,RMVar_hsa_circ_39648,RMVar_hsa_circ_199127,RMVar_hsa_circ_331314,RMVar_hsa_circ_352524,RMVar_hsa_circ_345172,RMVar_hsa_circ_300519,RMVar_hsa_circ_272046,RMVar_hsa_circ_275649,RMVar_hsa_circ_72099,RMVar_hsa_circ_199131,RMVar_hsa_circ_199133,RMVar_hsa_circ_199134,RMVar_hsa_circ_199132,RMVar_hsa_circ_199130,RMVar_hsa_circ_199135 19078 RMVar_ID_19078 Human_SNP_ID_68082807 A-to-I Human chr2 - 39275997 39275997 39275997 ATGGTCATGTGCAGCTGTAGTCCCAGCTACTCAGGAGGCTGAGACAGGAGAATCACTTAAACCCG ATGGTCATGTGCAGCTGTAGTCCCAGCTACTCCGGAGGCTGAGACAGGAGAATCACTTAAACCCG T G MAP4K3 Ensembl:ENSG00000011566 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs919423416 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569546 RMVar_hsa_circ_2324,RMVar_hsa_circ_81793,RMVar_hsa_circ_103557,RMVar_hsa_circ_199113,RMVar_hsa_circ_199114,RMVar_hsa_circ_127067,RMVar_hsa_circ_31511,RMVar_hsa_circ_83400,RMVar_hsa_circ_336403,RMVar_hsa_circ_199115,RMVar_hsa_circ_119828,RMVar_hsa_circ_35725,RMVar_hsa_circ_199116,RMVar_hsa_circ_199117,RMVar_hsa_circ_199118,RMVar_hsa_circ_349605,RMVar_hsa_circ_351418,RMVar_hsa_circ_310367,RMVar_hsa_circ_282430,RMVar_hsa_circ_50437,RMVar_hsa_circ_17038,RMVar_hsa_circ_199122,RMVar_hsa_circ_199123,RMVar_hsa_circ_199125,RMVar_hsa_circ_6619,RMVar_hsa_circ_19474,RMVar_hsa_circ_297253,RMVar_hsa_circ_318036,RMVar_hsa_circ_319562,RMVar_hsa_circ_107444,RMVar_hsa_circ_330081,RMVar_hsa_circ_362146,RMVar_hsa_circ_199124,RMVar_hsa_circ_351276,RMVar_hsa_circ_303416,RMVar_hsa_circ_70685,RMVar_hsa_circ_92589,RMVar_hsa_circ_34904,RMVar_hsa_circ_290890,RMVar_hsa_circ_199126,RMVar_hsa_circ_199128,RMVar_hsa_circ_39648,RMVar_hsa_circ_199127,RMVar_hsa_circ_331314,RMVar_hsa_circ_352524,RMVar_hsa_circ_345172,RMVar_hsa_circ_300519,RMVar_hsa_circ_272046,RMVar_hsa_circ_275649,RMVar_hsa_circ_72099,RMVar_hsa_circ_199131,RMVar_hsa_circ_199133,RMVar_hsa_circ_199134,RMVar_hsa_circ_199132,RMVar_hsa_circ_199130,RMVar_hsa_circ_199135 19079 RMVar_ID_19079 Human_SNP_ID_68085210 A-to-I Human chr2 - 39284299 39284299 39284299 GAAACAGCCGGGTGTGGTGGCAGGCGCCTGTAATCTCAGCTACTCAGGAGGCTGAGGCACGAGAA GAAACAGCCGGGTGTGGTGGCAGGCGCCTGTAGTCTCAGCTACTCAGGAGGCTGAGGCACGAGAA T C MAP4K3 Ensembl:ENSG00000011566 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170574207 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2324,RMVar_hsa_circ_81793,RMVar_hsa_circ_103557,RMVar_hsa_circ_199113,RMVar_hsa_circ_199114,RMVar_hsa_circ_127067,RMVar_hsa_circ_31511,RMVar_hsa_circ_83400,RMVar_hsa_circ_199115,RMVar_hsa_circ_119828,RMVar_hsa_circ_199117,RMVar_hsa_circ_199118,RMVar_hsa_circ_349605,RMVar_hsa_circ_50437,RMVar_hsa_circ_17038,RMVar_hsa_circ_318036,RMVar_hsa_circ_107444,RMVar_hsa_circ_362146,RMVar_hsa_circ_303416,RMVar_hsa_circ_70685,RMVar_hsa_circ_23715,RMVar_hsa_circ_92589,RMVar_hsa_circ_290890,RMVar_hsa_circ_199126,RMVar_hsa_circ_39648,RMVar_hsa_circ_199127,RMVar_hsa_circ_331314,RMVar_hsa_circ_352524,RMVar_hsa_circ_345172,RMVar_hsa_circ_300519,RMVar_hsa_circ_72099,RMVar_hsa_circ_199133,RMVar_hsa_circ_199134,RMVar_hsa_circ_199132,RMVar_hsa_circ_298507,RMVar_hsa_circ_328155,RMVar_hsa_circ_365576,RMVar_hsa_circ_199135,RMVar_hsa_circ_370508,RMVar_hsa_circ_339138,RMVar_hsa_circ_315433,RMVar_hsa_circ_320764,RMVar_hsa_circ_295920,RMVar_hsa_circ_71338,RMVar_hsa_circ_199136,RMVar_hsa_circ_199138,RMVar_hsa_circ_199140,RMVar_hsa_circ_199141,RMVar_hsa_circ_199139,RMVar_hsa_circ_199137,RMVar_hsa_circ_330079,RMVar_hsa_circ_199145,RMVar_hsa_circ_75548,RMVar_hsa_circ_348733,RMVar_hsa_circ_199146,RMVar_hsa_circ_199144 19080 RMVar_ID_19080 Human_SNP_ID_68085226 A-to-I Human chr2 - 39284349 39284349 39284349 CAAAACCAACCTCGCCAACATGGTAAAACCCCATCTCTACTACAAATACAGAAACAGCCGGGTGT CAAAACCAACCTCGCCAACATGGTAAAACCCCGTCTCTACTACAAATACAGAAACAGCCGGGTGT T C MAP4K3 Ensembl:ENSG00000011566 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973749096 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2324,RMVar_hsa_circ_81793,RMVar_hsa_circ_103557,RMVar_hsa_circ_199113,RMVar_hsa_circ_199114,RMVar_hsa_circ_127067,RMVar_hsa_circ_31511,RMVar_hsa_circ_83400,RMVar_hsa_circ_199115,RMVar_hsa_circ_119828,RMVar_hsa_circ_199117,RMVar_hsa_circ_199118,RMVar_hsa_circ_349605,RMVar_hsa_circ_50437,RMVar_hsa_circ_17038,RMVar_hsa_circ_318036,RMVar_hsa_circ_107444,RMVar_hsa_circ_362146,RMVar_hsa_circ_303416,RMVar_hsa_circ_70685,RMVar_hsa_circ_23715,RMVar_hsa_circ_92589,RMVar_hsa_circ_290890,RMVar_hsa_circ_199126,RMVar_hsa_circ_39648,RMVar_hsa_circ_199127,RMVar_hsa_circ_331314,RMVar_hsa_circ_352524,RMVar_hsa_circ_345172,RMVar_hsa_circ_300519,RMVar_hsa_circ_72099,RMVar_hsa_circ_199133,RMVar_hsa_circ_199134,RMVar_hsa_circ_199132,RMVar_hsa_circ_298507,RMVar_hsa_circ_328155,RMVar_hsa_circ_365576,RMVar_hsa_circ_199135,RMVar_hsa_circ_370508,RMVar_hsa_circ_339138,RMVar_hsa_circ_315433,RMVar_hsa_circ_320764,RMVar_hsa_circ_295920,RMVar_hsa_circ_71338,RMVar_hsa_circ_199136,RMVar_hsa_circ_199138,RMVar_hsa_circ_199140,RMVar_hsa_circ_199141,RMVar_hsa_circ_199139,RMVar_hsa_circ_199137,RMVar_hsa_circ_330079,RMVar_hsa_circ_199145,RMVar_hsa_circ_75548,RMVar_hsa_circ_348733,RMVar_hsa_circ_199146,RMVar_hsa_circ_199144 19081 RMVar_ID_19081 Human_SNP_ID_68085421 A-to-I Human chr2 - 39285017 39285017 39285017 ATGGTGGCATGCACCCATAATCCTAGCTGCTCAGGAGGCTGAGACAGGAGAATCACATGAGCCCA ATGGTGGCATGCACCCATAATCCTAGCTGCTCGGGAGGCTGAGACAGGAGAATCACATGAGCCCA T C MAP4K3 Ensembl:ENSG00000011566 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1365647329 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569549 RMVar_hsa_circ_2324,RMVar_hsa_circ_81793,RMVar_hsa_circ_103557,RMVar_hsa_circ_199113,RMVar_hsa_circ_199114,RMVar_hsa_circ_127067,RMVar_hsa_circ_31511,RMVar_hsa_circ_83400,RMVar_hsa_circ_199115,RMVar_hsa_circ_119828,RMVar_hsa_circ_199117,RMVar_hsa_circ_199118,RMVar_hsa_circ_349605,RMVar_hsa_circ_50437,RMVar_hsa_circ_17038,RMVar_hsa_circ_318036,RMVar_hsa_circ_107444,RMVar_hsa_circ_362146,RMVar_hsa_circ_303416,RMVar_hsa_circ_70685,RMVar_hsa_circ_23715,RMVar_hsa_circ_92589,RMVar_hsa_circ_290890,RMVar_hsa_circ_199126,RMVar_hsa_circ_39648,RMVar_hsa_circ_199127,RMVar_hsa_circ_331314,RMVar_hsa_circ_352524,RMVar_hsa_circ_345172,RMVar_hsa_circ_300519,RMVar_hsa_circ_72099,RMVar_hsa_circ_199133,RMVar_hsa_circ_199134,RMVar_hsa_circ_199132,RMVar_hsa_circ_298507,RMVar_hsa_circ_328155,RMVar_hsa_circ_365576,RMVar_hsa_circ_199135,RMVar_hsa_circ_370508,RMVar_hsa_circ_339138,RMVar_hsa_circ_315433,RMVar_hsa_circ_320764,RMVar_hsa_circ_295920,RMVar_hsa_circ_71338,RMVar_hsa_circ_199136,RMVar_hsa_circ_199138,RMVar_hsa_circ_199140,RMVar_hsa_circ_199141,RMVar_hsa_circ_199139,RMVar_hsa_circ_199137,RMVar_hsa_circ_330079,RMVar_hsa_circ_199145,RMVar_hsa_circ_75548,RMVar_hsa_circ_348733,RMVar_hsa_circ_199146,RMVar_hsa_circ_199144 19082 RMVar_ID_19082 Human_SNP_ID_68089506 A-to-I Human chr2 - 39298882 39298882 39298882 TGGCCCACTTCAACCTCCGCCTCCCGGGTTCAAGTGATTCTCATGCCCCAGCCTCCCAGTAGCTG TGGCCCACTTCAACCTCCGCCTCCCGGGTTCAGGTGATTCTCATGCCCCAGCCTCCCAGTAGCTG T C MAP4K3 Ensembl:ENSG00000011566 Protein coding intron GSE107867 ASD brains,frontal_cortex;ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1231435169 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6394,RMVar_hsa_circ_127067,RMVar_hsa_circ_31511,RMVar_hsa_circ_83400,RMVar_hsa_circ_199115,RMVar_hsa_circ_119828,RMVar_hsa_circ_199117,RMVar_hsa_circ_199118,RMVar_hsa_circ_50437,RMVar_hsa_circ_17038,RMVar_hsa_circ_107444,RMVar_hsa_circ_362146,RMVar_hsa_circ_70685,RMVar_hsa_circ_23715,RMVar_hsa_circ_92589,RMVar_hsa_circ_199126,RMVar_hsa_circ_39648,RMVar_hsa_circ_331314,RMVar_hsa_circ_352524,RMVar_hsa_circ_72099,RMVar_hsa_circ_199134,RMVar_hsa_circ_328155,RMVar_hsa_circ_365576,RMVar_hsa_circ_199135,RMVar_hsa_circ_370508,RMVar_hsa_circ_339138,RMVar_hsa_circ_315433,RMVar_hsa_circ_199136,RMVar_hsa_circ_199138,RMVar_hsa_circ_199137,RMVar_hsa_circ_52845,RMVar_hsa_circ_199145,RMVar_hsa_circ_75548,RMVar_hsa_circ_199146,RMVar_hsa_circ_328002,RMVar_hsa_circ_199147,RMVar_hsa_circ_292951,RMVar_hsa_circ_332598,RMVar_hsa_circ_372057,RMVar_hsa_circ_199155,RMVar_hsa_circ_199153,RMVar_hsa_circ_291856,RMVar_hsa_circ_335996,RMVar_hsa_circ_199152,RMVar_hsa_circ_335973,RMVar_hsa_circ_199154,RMVar_hsa_circ_115351 19083 RMVar_ID_19083 Human_SNP_ID_68139368 A-to-I Human chr2 + 39474007 39474007 39474007 AAAATTAGCCGGATGTGCTGGCACATACCTGTAGTCCCAGCTACTCAGGAAGCTGAGCTGAGGAG AAAATTAGCCGGATGTGCTGGCACATACCTGTTGTCCCAGCTACTCAGGAAGCTGAGCTGAGGAG A T MAP4K3-DT Ensembl:ENSG00000231312 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223011494 Functional Loss SNV dbSNP153 33..33 33 - - - 19084 RMVar_ID_19084 Human_SNP_ID_68139746 A-to-I Human chr2 + 39475328 39475328 39475328 TTCATTGTTCTTTCTTTCTTTTAAAAATTTCTATGACTGAGCTGGACATGGTAGCTCACACCTGT TTCATTGTTCTTTCTTTCTTTTAAAAATTTCTGTGACTGAGCTGGACATGGTAGCTCACACCTGT A G MAP4K3-DT Ensembl:ENSG00000231312 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910657564 Functional Loss SNV dbSNP153 33..33 33 - - - 19085 RMVar_ID_19085 Human_SNP_ID_68140197 A-to-I Human chr2 + 39477004 39477004 39477004 ATGGAGTCTTGCTCCGTTGCCCAGGCTGGAGTATAGTGGTGTGATCTCGGCTCACTGCAACCTTC ATGGAGTCTTGCTCCGTTGCCCAGGCTGGAGTGTAGTGGTGTGATCTCGGCTCACTGCAACCTTC A G MAP4K3-DT Ensembl:ENSG00000231312 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1426791817 Functional Loss SNV dbSNP153 33..33 33 - - - 19086 RMVar_ID_19086 Human_SNP_ID_68140264 A-to-I Human chr2 + 39477198 39477198 39477198 GTCTCAAACTCCTGACCTCAAGTGATCCTCCCACCTCAGCCTCCCAAAGTGCTGTGATTACAGAA GTCTCAAACTCCTGACCTCAAGTGATCCTCCCGCCTCAGCCTCCCAAAGTGCTGTGATTACAGAA A G MAP4K3-DT Ensembl:ENSG00000231312 lincRNA intron GSE47997;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;Bronchiolar epithelium,BERP35T1 cell line - 23474544,31158229 RNA-Seq:(High) rs1271611558 Functional Loss SNV dbSNP153 33..33 33 - - - 19087 RMVar_ID_19087 Human_SNP_ID_68140265 A-to-I Human chr2 + 39477203 39477203 39477203 AAACTCCTGACCTCAAGTGATCCTCCCACCTCAGCCTCCCAAAGTGCTGTGATTACAGAAGTGAG AAACTCCTGACCTCAAGTGATCCTCCCACCTCGGCCTCCCAAAGTGCTGTGATTACAGAAGTGAG A G MAP4K3-DT Ensembl:ENSG00000231312 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1224829477 Functional Loss SNV dbSNP153 33..33 33 - - - 19088 RMVar_ID_19088 Human_SNP_ID_68141864 A-to-I Human chr2 + 39482273 39482273 39482273 GGAGATCACTGCAACCTCTGCCTCCAGGGTGCAAGTGATTCTCCTGCCTCAGGCTCCCGAGGAGC GGAGATCACTGCAACCTCTGCCTCCAGGGTGCGAGTGATTCTCCTGCCTCAGGCTCCCGAGGAGC A G MAP4K3-DT Ensembl:ENSG00000231312 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1422662675 Functional Loss SNV dbSNP153 33..33 33 - - - 19089 RMVar_ID_19089 Human_SNP_ID_68141924 A-to-I Human chr2 + 39482443 39482443 39482443 GTGATCCACCCGCCTTGGCCTCCCAAAGTGCTAGGATTACAGGCGGCAGCCACCACACCTGGCCT GTGATCCACCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGGCAGCCACCACACCTGGCCT A G MAP4K3-DT Ensembl:ENSG00000231312 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1201411272 Functional Loss SNV dbSNP153 33..33 33 - - - 19090 RMVar_ID_19090 Human_SNP_ID_68141997 A-to-I Human chr2 + 39482707 39482706 39482708 ATTTAAGTTTTTATTCTTTGTTTTTTTGAGACAGAGTCTCACTTTGTTGCCCAGGCTGGAGTGCC ATTTAAGTTTTTATTCTTTGTTTTTTTGAGAC__AGTCTCACTTTGTTGCCCAGGCTGGAGTGCC CAG C MAP4K3-DT Ensembl:ENSG00000231312 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1420702940 Functional Loss DEL dbSNP153 33..34 33 - - - 19091 RMVar_ID_19091 Human_SNP_ID_68141999 A-to-I Human chr2 + 39482715 39482715 39482715 TTTTATTCTTTGTTTTTTTGAGACAGAGTCTCACTTTGTTGCCCAGGCTGGAGTGCCATGGCGTG TTTTATTCTTTGTTTTTTTGAGACAGAGTCTCGCTTTGTTGCCCAGGCTGGAGTGCCATGGCGTG A G MAP4K3-DT Ensembl:ENSG00000231312 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs921889191 Functional Loss SNV dbSNP153 33..33 33 - - - 19092 RMVar_ID_19092 Human_SNP_ID_68143919 A-to-I Human chr2 + 39488779 39488779 39488779 GTAGAAACAGGGTTTCACATGTTGCCCAGACTAGTCATGACCTCCTTAGCTCAAGTGAGCCACCT GTAGAAACAGGGTTTCACATGTTGCCCAGACTTGTCATGACCTCCTTAGCTCAAGTGAGCCACCT A T MAP4K3-DT Ensembl:ENSG00000231312 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1486556140 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17699081 19093 RMVar_ID_19093 Human_SNP_ID_68222432 A-to-I Human chr2 - 39775248 39775248 39775248 TCGTGACAGGATCAGGCTCTGTCACTCAGGCTAGGGAACAGTGGCGTGATCACAGATCACTGCAA TCGTGACAGGATCAGGCTCTGTCACTCAGGCTGGGGAACAGTGGCGTGATCACAGATCACTGCAA T C THUMPD2 Ensembl:ENSG00000138050 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs147017692 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6920081,Human_RBP_ID_13886323 19094 RMVar_ID_19094 Human_SNP_ID_68343595 A-to-I Human chr2 + 40154799 40154799 40154799 TGATCCTACTGCCTCAGCCTCCTGAGTAGCTGAGACTACAGGCATGCACTATCACACCCGGCTAA TGATCCTACTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCATGCACTATCACACCCGGCTAA A G SLC8A1-AS1 Ensembl:ENSG00000227028 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs959890652 Functional Loss SNV dbSNP153 33..33 33 - - - 19095 RMVar_ID_19095 Human_SNP_ID_68366924 A-to-I Human chr2 - 40232100 40232100 40232100 GCTTTGACCTTCAGTGATCTACCACCTCTCCCAAGCCTTGCTTGATTTTTTGAACTGGACCCATT GCTTTGACCTTCAGTGATCTACCACCTCTCCCTAGCCTTGCTTGATTTTTTGAACTGGACCCATT T A SLC8A1 Ensembl:ENSG00000183023 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs969222072 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_199211,RMVar_hsa_circ_114004 19096 RMVar_ID_19096 Human_SNP_ID_68401178 A-to-I Human chr2 - 40333869 40333869 40333869 TAATTTTGTATTTTTAGTACAAACAGGGTTTCACCATGTTGGTCCGGCTGGTCTCAAACCCCTGA TAATTTTGTATTTTTAGTACAAACAGGGTTTCGCCATGTTGGTCCGGCTGGTCTCAAACCCCTGA T C SLC8A1 Ensembl:ENSG00000183023 Protein coding intron GSE107867 ASD brains,frontal_cortex;ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1230699240 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_199211,RMVar_hsa_circ_114004 19097 RMVar_ID_19097 Human_SNP_ID_68982622 A-to-I Human chr2 + 42209728 42209728 42209728 GAGGCCTGTGGATCACCTGAGGTCAGGAGTTCAAGACCAGCCTGACCAACACGGAGAAACCCGGT GAGGCCTGTGGATCACCTGAGGTCAGGAGTTCGAGACCAGCCTGACCAACACGGAGAAACCCGGT A G EML4 Ensembl:ENSG00000143924 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1247543122 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117094,RMVar_hsa_circ_199225 19098 RMVar_ID_19098 Human_SNP_ID_68998822 A-to-I Human chr2 + 42258500 42258500 42258500 TCGGCTCACCGCAACCTGCACCTCCCGTGTTCAAGAGATTCTCCTGCTGCAGCACCCGGAGTAGC TCGGCTCACCGCAACCTGCACCTCCCGTGTTCCAGAGATTCTCCTGCTGCAGCACCCGGAGTAGC A C EML4 Ensembl:ENSG00000143924 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs78899455 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569557,Human_RBP_ID_23872013 GWAS_ID_1660 RMVar_hsa_circ_56341,RMVar_hsa_circ_125611,RMVar_hsa_circ_117094,RMVar_hsa_circ_199225,RMVar_hsa_circ_199227,RMVar_hsa_circ_69785,RMVar_hsa_circ_47101,RMVar_hsa_circ_326879,RMVar_hsa_circ_352760,RMVar_hsa_circ_355543,RMVar_hsa_circ_334898,RMVar_hsa_circ_298302,RMVar_hsa_circ_56385,RMVar_hsa_circ_31678,RMVar_hsa_circ_55472,RMVar_hsa_circ_21554,RMVar_hsa_circ_199229 19099 RMVar_ID_19099 Human_SNP_ID_68998823 A-to-I Human chr2 + 42258500 42258500 42258500 TCGGCTCACCGCAACCTGCACCTCCCGTGTTCAAGAGATTCTCCTGCTGCAGCACCCGGAGTAGC TCGGCTCACCGCAACCTGCACCTCCCGTGTTCGAGAGATTCTCCTGCTGCAGCACCCGGAGTAGC A G EML4 Ensembl:ENSG00000143924 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs78899455 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569557,Human_RBP_ID_23872013 GWAS_ID_1660 RMVar_hsa_circ_56341,RMVar_hsa_circ_125611,RMVar_hsa_circ_117094,RMVar_hsa_circ_199225,RMVar_hsa_circ_199227,RMVar_hsa_circ_69785,RMVar_hsa_circ_47101,RMVar_hsa_circ_326879,RMVar_hsa_circ_352760,RMVar_hsa_circ_355543,RMVar_hsa_circ_334898,RMVar_hsa_circ_298302,RMVar_hsa_circ_56385,RMVar_hsa_circ_31678,RMVar_hsa_circ_55472,RMVar_hsa_circ_21554,RMVar_hsa_circ_199229 19100 RMVar_ID_19100 Human_SNP_ID_69002437 A-to-I Human chr2 + 42268706 42268706 42268706 GCAGTCCTCCCATCTCTACCTCCCAAAGCGTTAGGATTATAGCTGTGAGCCGCCGCACCTGGCCT GCAGTCCTCCCATCTCTACCTCCCAAAGCGTTCGGATTATAGCTGTGAGCCGCCGCACCTGGCCT A C EML4 Ensembl:ENSG00000143924 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1438361560 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13887586 RMVar_hsa_circ_14521,RMVar_hsa_circ_56341,RMVar_hsa_circ_125611,RMVar_hsa_circ_117094,RMVar_hsa_circ_199225,RMVar_hsa_circ_199227,RMVar_hsa_circ_47101,RMVar_hsa_circ_326879,RMVar_hsa_circ_355543,RMVar_hsa_circ_298302,RMVar_hsa_circ_56385,RMVar_hsa_circ_31678,RMVar_hsa_circ_55472,RMVar_hsa_circ_21554,RMVar_hsa_circ_348167,RMVar_hsa_circ_353038,RMVar_hsa_circ_199229,RMVar_hsa_circ_352446,RMVar_hsa_circ_321865,RMVar_hsa_circ_56098,RMVar_hsa_circ_110419,RMVar_hsa_circ_32060,RMVar_hsa_circ_325011,RMVar_hsa_circ_363304,RMVar_hsa_circ_375811,RMVar_hsa_circ_51574,RMVar_hsa_circ_199232,RMVar_hsa_circ_199233,RMVar_hsa_circ_199231,RMVar_hsa_circ_199234 19101 RMVar_ID_19101 Human_SNP_ID_69002438 A-to-I Human chr2 + 42268706 42268706 42268706 GCAGTCCTCCCATCTCTACCTCCCAAAGCGTTAGGATTATAGCTGTGAGCCGCCGCACCTGGCCT GCAGTCCTCCCATCTCTACCTCCCAAAGCGTTGGGATTATAGCTGTGAGCCGCCGCACCTGGCCT A G EML4 Ensembl:ENSG00000143924 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1438361560 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13887586 RMVar_hsa_circ_14521,RMVar_hsa_circ_56341,RMVar_hsa_circ_125611,RMVar_hsa_circ_117094,RMVar_hsa_circ_199225,RMVar_hsa_circ_199227,RMVar_hsa_circ_47101,RMVar_hsa_circ_326879,RMVar_hsa_circ_355543,RMVar_hsa_circ_298302,RMVar_hsa_circ_56385,RMVar_hsa_circ_31678,RMVar_hsa_circ_55472,RMVar_hsa_circ_21554,RMVar_hsa_circ_348167,RMVar_hsa_circ_353038,RMVar_hsa_circ_199229,RMVar_hsa_circ_352446,RMVar_hsa_circ_321865,RMVar_hsa_circ_56098,RMVar_hsa_circ_110419,RMVar_hsa_circ_32060,RMVar_hsa_circ_325011,RMVar_hsa_circ_363304,RMVar_hsa_circ_375811,RMVar_hsa_circ_51574,RMVar_hsa_circ_199232,RMVar_hsa_circ_199233,RMVar_hsa_circ_199231,RMVar_hsa_circ_199234 19102 RMVar_ID_19102 Human_SNP_ID_69002439 A-to-I Human chr2 + 42268714 42268714 42268714 CCCATCTCTACCTCCCAAAGCGTTAGGATTATAGCTGTGAGCCGCCGCACCTGGCCTACATTTTT CCCATCTCTACCTCCCAAAGCGTTAGGATTATGGCTGTGAGCCGCCGCACCTGGCCTACATTTTT A G EML4 Ensembl:ENSG00000143924 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1419554746 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13887586 RMVar_hsa_circ_14521,RMVar_hsa_circ_56341,RMVar_hsa_circ_125611,RMVar_hsa_circ_117094,RMVar_hsa_circ_199225,RMVar_hsa_circ_199227,RMVar_hsa_circ_47101,RMVar_hsa_circ_326879,RMVar_hsa_circ_355543,RMVar_hsa_circ_298302,RMVar_hsa_circ_56385,RMVar_hsa_circ_31678,RMVar_hsa_circ_55472,RMVar_hsa_circ_21554,RMVar_hsa_circ_348167,RMVar_hsa_circ_353038,RMVar_hsa_circ_199229,RMVar_hsa_circ_352446,RMVar_hsa_circ_321865,RMVar_hsa_circ_56098,RMVar_hsa_circ_110419,RMVar_hsa_circ_32060,RMVar_hsa_circ_325011,RMVar_hsa_circ_363304,RMVar_hsa_circ_375811,RMVar_hsa_circ_51574,RMVar_hsa_circ_199232,RMVar_hsa_circ_199233,RMVar_hsa_circ_199231,RMVar_hsa_circ_199234 19103 RMVar_ID_19103 Human_SNP_ID_69003576 A-to-I Human chr2 + 42272504 42272504 42272504 TTCAGGGGTTTTTTTCATTTGTTTTGGTCTCAAACTCCTGACCTCGGGTGATCTGCCCACCTTGG TTCAGGGGTTTTTTTCATTTGTTTTGGTCTCAGACTCCTGACCTCGGGTGATCTGCCCACCTTGG A G EML4 Ensembl:ENSG00000143924 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1267801501 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14521,RMVar_hsa_circ_56341,RMVar_hsa_circ_125611,RMVar_hsa_circ_117094,RMVar_hsa_circ_199225,RMVar_hsa_circ_199227,RMVar_hsa_circ_47101,RMVar_hsa_circ_326879,RMVar_hsa_circ_355543,RMVar_hsa_circ_298302,RMVar_hsa_circ_56385,RMVar_hsa_circ_31678,RMVar_hsa_circ_55472,RMVar_hsa_circ_21554,RMVar_hsa_circ_348167,RMVar_hsa_circ_353038,RMVar_hsa_circ_199229,RMVar_hsa_circ_352446,RMVar_hsa_circ_321865,RMVar_hsa_circ_56098,RMVar_hsa_circ_110419,RMVar_hsa_circ_32060,RMVar_hsa_circ_325011,RMVar_hsa_circ_363304,RMVar_hsa_circ_375811,RMVar_hsa_circ_51574,RMVar_hsa_circ_199232,RMVar_hsa_circ_199233,RMVar_hsa_circ_199231,RMVar_hsa_circ_199234 19104 RMVar_ID_19104 Human_SNP_ID_69005512 A-to-I Human chr2 + 42278747 42278747 42278747 CCTGAGGTCATGAGTTCAAGATCAGCCTGACCAACATGGTGAAACCCCATCTCTACTAAAAATAC CCTGAGGTCATGAGTTCAAGATCAGCCTGACCGACATGGTGAAACCCCATCTCTACTAAAAATAC A G EML4 Ensembl:ENSG00000143924 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1274232810 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14521,RMVar_hsa_circ_56341,RMVar_hsa_circ_125611,RMVar_hsa_circ_117094,RMVar_hsa_circ_199225,RMVar_hsa_circ_199227,RMVar_hsa_circ_47101,RMVar_hsa_circ_326879,RMVar_hsa_circ_355543,RMVar_hsa_circ_298302,RMVar_hsa_circ_56385,RMVar_hsa_circ_31678,RMVar_hsa_circ_55472,RMVar_hsa_circ_21554,RMVar_hsa_circ_348167,RMVar_hsa_circ_353038,RMVar_hsa_circ_199229,RMVar_hsa_circ_352446,RMVar_hsa_circ_321865,RMVar_hsa_circ_56098,RMVar_hsa_circ_110419,RMVar_hsa_circ_32060,RMVar_hsa_circ_325011,RMVar_hsa_circ_363304,RMVar_hsa_circ_375811,RMVar_hsa_circ_51574,RMVar_hsa_circ_199232,RMVar_hsa_circ_199233,RMVar_hsa_circ_199231,RMVar_hsa_circ_199234 19105 RMVar_ID_19105 Human_SNP_ID_69005810 A-to-I Human chr2 + 42279587 42279587 42279587 TCACGCCATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGTGCCCGCCATCATGCCTG TCACGCCATTCTCCTGCCTCAGCCTCCCAAGTCGCTGGGACTACAGGTGCCCGCCATCATGCCTG A C EML4 Ensembl:ENSG00000143924 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1365864142 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_143744 RMVar_hsa_circ_14521,RMVar_hsa_circ_56341,RMVar_hsa_circ_125611,RMVar_hsa_circ_117094,RMVar_hsa_circ_199225,RMVar_hsa_circ_199227,RMVar_hsa_circ_47101,RMVar_hsa_circ_326879,RMVar_hsa_circ_355543,RMVar_hsa_circ_298302,RMVar_hsa_circ_56385,RMVar_hsa_circ_31678,RMVar_hsa_circ_55472,RMVar_hsa_circ_21554,RMVar_hsa_circ_348167,RMVar_hsa_circ_353038,RMVar_hsa_circ_199229,RMVar_hsa_circ_352446,RMVar_hsa_circ_321865,RMVar_hsa_circ_56098,RMVar_hsa_circ_110419,RMVar_hsa_circ_32060,RMVar_hsa_circ_325011,RMVar_hsa_circ_363304,RMVar_hsa_circ_375811,RMVar_hsa_circ_51574,RMVar_hsa_circ_199232,RMVar_hsa_circ_199233,RMVar_hsa_circ_199231,RMVar_hsa_circ_199234 19106 RMVar_ID_19106 Human_SNP_ID_69005813 A-to-I Human chr2 + 42279599 42279599 42279599 CCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGTGCCCGCCATCATGCCTGGCTAATTTTTTT CCTGCCTCAGCCTCCCAAGTAGCTGGGACTACTGGTGCCCGCCATCATGCCTGGCTAATTTTTTT A T EML4 Ensembl:ENSG00000143924 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs529611546 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_143744 RMVar_hsa_circ_14521,RMVar_hsa_circ_56341,RMVar_hsa_circ_125611,RMVar_hsa_circ_117094,RMVar_hsa_circ_199225,RMVar_hsa_circ_199227,RMVar_hsa_circ_47101,RMVar_hsa_circ_326879,RMVar_hsa_circ_355543,RMVar_hsa_circ_298302,RMVar_hsa_circ_56385,RMVar_hsa_circ_31678,RMVar_hsa_circ_55472,RMVar_hsa_circ_21554,RMVar_hsa_circ_348167,RMVar_hsa_circ_353038,RMVar_hsa_circ_199229,RMVar_hsa_circ_352446,RMVar_hsa_circ_321865,RMVar_hsa_circ_56098,RMVar_hsa_circ_110419,RMVar_hsa_circ_32060,RMVar_hsa_circ_325011,RMVar_hsa_circ_363304,RMVar_hsa_circ_375811,RMVar_hsa_circ_51574,RMVar_hsa_circ_199232,RMVar_hsa_circ_199233,RMVar_hsa_circ_199231,RMVar_hsa_circ_199234 19107 RMVar_ID_19107 Human_SNP_ID_69006818 A-to-I Human chr2 + 42282493 42282493 42282493 TCACTGTAGCCTTGACCTGACCTCCTGGGCTCAAGTGATTCTCCCACCTCAGACTCCCAAGTAGC TCACTGTAGCCTTGACCTGACCTCCTGGGCTCCAGTGATTCTCCCACCTCAGACTCCCAAGTAGC A C EML4 Ensembl:ENSG00000143924 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1280716642 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14521,RMVar_hsa_circ_56341,RMVar_hsa_circ_125611,RMVar_hsa_circ_117094,RMVar_hsa_circ_199225,RMVar_hsa_circ_199227,RMVar_hsa_circ_47101,RMVar_hsa_circ_326879,RMVar_hsa_circ_355543,RMVar_hsa_circ_56385,RMVar_hsa_circ_31678,RMVar_hsa_circ_55472,RMVar_hsa_circ_21554,RMVar_hsa_circ_348167,RMVar_hsa_circ_353038,RMVar_hsa_circ_199229,RMVar_hsa_circ_352446,RMVar_hsa_circ_321865,RMVar_hsa_circ_56098,RMVar_hsa_circ_6374,RMVar_hsa_circ_110419,RMVar_hsa_circ_32060,RMVar_hsa_circ_325011,RMVar_hsa_circ_363304,RMVar_hsa_circ_375811,RMVar_hsa_circ_51574,RMVar_hsa_circ_199232,RMVar_hsa_circ_199233,RMVar_hsa_circ_199231,RMVar_hsa_circ_298871,RMVar_hsa_circ_311557,RMVar_hsa_circ_357628,RMVar_hsa_circ_199234,RMVar_hsa_circ_365797,RMVar_hsa_circ_344951,RMVar_hsa_circ_310467,RMVar_hsa_circ_68547,RMVar_hsa_circ_14610,RMVar_hsa_circ_199237,RMVar_hsa_circ_199239,RMVar_hsa_circ_199240,RMVar_hsa_circ_199238,RMVar_hsa_circ_199236 19108 RMVar_ID_19108 Human_SNP_ID_69010337 A-to-I Human chr2 + 42293303 42293301 42293303 CTAATTTACTTTTTGTAGAGACAGGTCTCACTATGTTGCACAGTTGATCTCTAACTCCTGGCCTC CTAATTTACTTTTTGTAGAGACAGGTCTCAC__TGTTGCACAGTTGATCTCTAACTCCTGGCCTC CTA C EML4 Ensembl:ENSG00000143924 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs778627134 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_13888058 RMVar_hsa_circ_54812,RMVar_hsa_circ_14521,RMVar_hsa_circ_56341,RMVar_hsa_circ_117094,RMVar_hsa_circ_199225,RMVar_hsa_circ_326879,RMVar_hsa_circ_56385,RMVar_hsa_circ_55472,RMVar_hsa_circ_21554,RMVar_hsa_circ_199229,RMVar_hsa_circ_321865,RMVar_hsa_circ_56098,RMVar_hsa_circ_110419,RMVar_hsa_circ_32060,RMVar_hsa_circ_363304,RMVar_hsa_circ_375811,RMVar_hsa_circ_199232,RMVar_hsa_circ_199233,RMVar_hsa_circ_311557,RMVar_hsa_circ_357628,RMVar_hsa_circ_199234,RMVar_hsa_circ_365797,RMVar_hsa_circ_344951,RMVar_hsa_circ_14610,RMVar_hsa_circ_109399,RMVar_hsa_circ_199239,RMVar_hsa_circ_199240,RMVar_hsa_circ_199238,RMVar_hsa_circ_126384,RMVar_hsa_circ_371955,RMVar_hsa_circ_305745,RMVar_hsa_circ_199241,RMVar_hsa_circ_199242,RMVar_hsa_circ_199243,RMVar_hsa_circ_357444,RMVar_hsa_circ_360334,RMVar_hsa_circ_63929,RMVar_hsa_circ_65803,RMVar_hsa_circ_61607,RMVar_hsa_circ_36620,RMVar_hsa_circ_306973,RMVar_hsa_circ_199244,RMVar_hsa_circ_331583,RMVar_hsa_circ_276862,RMVar_hsa_circ_199246,RMVar_hsa_circ_199247,RMVar_hsa_circ_199249,RMVar_hsa_circ_70330,RMVar_hsa_circ_376204,RMVar_hsa_circ_199248,RMVar_hsa_circ_118202,RMVar_hsa_circ_199250 19109 RMVar_ID_19109 Human_SNP_ID_69010340 A-to-I Human chr2 + 42293303 42293303 42293303 CTAATTTACTTTTTGTAGAGACAGGTCTCACTATGTTGCACAGTTGATCTCTAACTCCTGGCCTC CTAATTTACTTTTTGTAGAGACAGGTCTCACTGTGTTGCACAGTTGATCTCTAACTCCTGGCCTC A G EML4 Ensembl:ENSG00000143924 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs565991047 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13888058 RMVar_hsa_circ_54812,RMVar_hsa_circ_14521,RMVar_hsa_circ_56341,RMVar_hsa_circ_117094,RMVar_hsa_circ_199225,RMVar_hsa_circ_326879,RMVar_hsa_circ_56385,RMVar_hsa_circ_55472,RMVar_hsa_circ_21554,RMVar_hsa_circ_199229,RMVar_hsa_circ_321865,RMVar_hsa_circ_56098,RMVar_hsa_circ_110419,RMVar_hsa_circ_32060,RMVar_hsa_circ_363304,RMVar_hsa_circ_375811,RMVar_hsa_circ_199232,RMVar_hsa_circ_199233,RMVar_hsa_circ_311557,RMVar_hsa_circ_357628,RMVar_hsa_circ_199234,RMVar_hsa_circ_365797,RMVar_hsa_circ_344951,RMVar_hsa_circ_14610,RMVar_hsa_circ_109399,RMVar_hsa_circ_199239,RMVar_hsa_circ_199240,RMVar_hsa_circ_199238,RMVar_hsa_circ_126384,RMVar_hsa_circ_371955,RMVar_hsa_circ_305745,RMVar_hsa_circ_199241,RMVar_hsa_circ_199242,RMVar_hsa_circ_199243,RMVar_hsa_circ_357444,RMVar_hsa_circ_360334,RMVar_hsa_circ_63929,RMVar_hsa_circ_65803,RMVar_hsa_circ_61607,RMVar_hsa_circ_36620,RMVar_hsa_circ_306973,RMVar_hsa_circ_199244,RMVar_hsa_circ_331583,RMVar_hsa_circ_276862,RMVar_hsa_circ_199246,RMVar_hsa_circ_199247,RMVar_hsa_circ_199249,RMVar_hsa_circ_70330,RMVar_hsa_circ_376204,RMVar_hsa_circ_199248,RMVar_hsa_circ_118202,RMVar_hsa_circ_199250 19110 RMVar_ID_19110 Human_SNP_ID_69014835 A-to-I Human chr2 + 42307838 42307838 42307838 CACCATACCCAGCTAATTTTTGTATTTCTAGTAGAGACAGGGTTTCGCCATGTTGGCCAGGCTGG CACCATACCCAGCTAATTTTTGTATTTCTAGTGGAGACAGGGTTTCGCCATGTTGGCCAGGCTGG A G EML4 Ensembl:ENSG00000143924 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1445590326 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56385,RMVar_hsa_circ_21554,RMVar_hsa_circ_56098,RMVar_hsa_circ_357628,RMVar_hsa_circ_14610,RMVar_hsa_circ_199240,RMVar_hsa_circ_126384,RMVar_hsa_circ_199241,RMVar_hsa_circ_357444,RMVar_hsa_circ_63929,RMVar_hsa_circ_61607,RMVar_hsa_circ_331583,RMVar_hsa_circ_312653,RMVar_hsa_circ_328416,RMVar_hsa_circ_49198,RMVar_hsa_circ_52739,RMVar_hsa_circ_199252,RMVar_hsa_circ_199251,RMVar_hsa_circ_118917,RMVar_hsa_circ_64669,RMVar_hsa_circ_290992,RMVar_hsa_circ_91940,RMVar_hsa_circ_199258,RMVar_hsa_circ_199259,RMVar_hsa_circ_199260 19111 RMVar_ID_19111 Human_SNP_ID_69014999 A-to-I Human chr2 + 42308361 42308361 42308361 AACCCTGTCTTTACAAGAAAAATTTTAAAATTAGCCAGGCGTGGTGGTGTGTGCACCTGTAGTCC AACCCTGTCTTTACAAGAAAAATTTTAAAATTTGCCAGGCGTGGTGGTGTGTGCACCTGTAGTCC A T EML4 Ensembl:ENSG00000143924 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1043458519 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56385,RMVar_hsa_circ_21554,RMVar_hsa_circ_56098,RMVar_hsa_circ_357628,RMVar_hsa_circ_14610,RMVar_hsa_circ_199240,RMVar_hsa_circ_126384,RMVar_hsa_circ_199241,RMVar_hsa_circ_357444,RMVar_hsa_circ_63929,RMVar_hsa_circ_61607,RMVar_hsa_circ_331583,RMVar_hsa_circ_312653,RMVar_hsa_circ_328416,RMVar_hsa_circ_49198,RMVar_hsa_circ_52739,RMVar_hsa_circ_199252,RMVar_hsa_circ_199251,RMVar_hsa_circ_118917,RMVar_hsa_circ_64669,RMVar_hsa_circ_290992,RMVar_hsa_circ_91940,RMVar_hsa_circ_199258,RMVar_hsa_circ_199259,RMVar_hsa_circ_199260 19112 RMVar_ID_19112 Human_SNP_ID_69015007 A-to-I Human chr2 + 42308389 42308389 42308389 AATTAGCCAGGCGTGGTGGTGTGTGCACCTGTAGTCCCTGCTACTCGGGAGGCTGAGGCAGGAGG AATTAGCCAGGCGTGGTGGTGTGTGCACCTGTTGTCCCTGCTACTCGGGAGGCTGAGGCAGGAGG A T EML4 Ensembl:ENSG00000143924 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1197063423 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56385,RMVar_hsa_circ_21554,RMVar_hsa_circ_56098,RMVar_hsa_circ_357628,RMVar_hsa_circ_14610,RMVar_hsa_circ_199240,RMVar_hsa_circ_126384,RMVar_hsa_circ_199241,RMVar_hsa_circ_357444,RMVar_hsa_circ_63929,RMVar_hsa_circ_61607,RMVar_hsa_circ_331583,RMVar_hsa_circ_312653,RMVar_hsa_circ_328416,RMVar_hsa_circ_49198,RMVar_hsa_circ_52739,RMVar_hsa_circ_199252,RMVar_hsa_circ_199251,RMVar_hsa_circ_118917,RMVar_hsa_circ_64669,RMVar_hsa_circ_290992,RMVar_hsa_circ_91940,RMVar_hsa_circ_199258,RMVar_hsa_circ_199259,RMVar_hsa_circ_199260 19113 RMVar_ID_19113 Human_SNP_ID_69015627 A-to-I Human chr2 + 42310370 42310370 42310370 TTCCCCTTCCCCTTCCCTTTTCCCTTTTGCAGAGTCTTGCTCTGTCTCCCAGGCTGGAGTGCAGT TTCCCCTTCCCCTTCCCTTTTCCCTTTTGCAGCGTCTTGCTCTGTCTCCCAGGCTGGAGTGCAGT A C EML4 Ensembl:ENSG00000143924 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs116220300 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5131562,Human_RBP_ID_17084484,Human_RBP_ID_17569254,Human_RBP_ID_18947761 RMVar_hsa_circ_56385,RMVar_hsa_circ_21554,RMVar_hsa_circ_56098,RMVar_hsa_circ_357628,RMVar_hsa_circ_14610,RMVar_hsa_circ_199240,RMVar_hsa_circ_126384,RMVar_hsa_circ_199241,RMVar_hsa_circ_357444,RMVar_hsa_circ_63929,RMVar_hsa_circ_61607,RMVar_hsa_circ_331583,RMVar_hsa_circ_312653,RMVar_hsa_circ_328416,RMVar_hsa_circ_49198,RMVar_hsa_circ_52739,RMVar_hsa_circ_199252,RMVar_hsa_circ_199251,RMVar_hsa_circ_118917,RMVar_hsa_circ_64669,RMVar_hsa_circ_290992,RMVar_hsa_circ_91940,RMVar_hsa_circ_199258,RMVar_hsa_circ_199259,RMVar_hsa_circ_199260 19114 RMVar_ID_19114 Human_SNP_ID_69015666 A-to-I Human chr2 + 42310487 42310487 42310487 CATGCCTCAACCTCCCAGGTAGCTGGGACTACAAGCGTGCACCACCATGCCTGGCTAATTTTTGT CATGCCTCAACCTCCCAGGTAGCTGGGACTACTAGCGTGCACCACCATGCCTGGCTAATTTTTGT A T EML4 Ensembl:ENSG00000143924 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1396558222 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56385,RMVar_hsa_circ_21554,RMVar_hsa_circ_56098,RMVar_hsa_circ_357628,RMVar_hsa_circ_14610,RMVar_hsa_circ_199240,RMVar_hsa_circ_126384,RMVar_hsa_circ_199241,RMVar_hsa_circ_357444,RMVar_hsa_circ_63929,RMVar_hsa_circ_61607,RMVar_hsa_circ_331583,RMVar_hsa_circ_312653,RMVar_hsa_circ_328416,RMVar_hsa_circ_49198,RMVar_hsa_circ_52739,RMVar_hsa_circ_199252,RMVar_hsa_circ_199251,RMVar_hsa_circ_118917,RMVar_hsa_circ_64669,RMVar_hsa_circ_290992,RMVar_hsa_circ_91940,RMVar_hsa_circ_199258,RMVar_hsa_circ_199259,RMVar_hsa_circ_199260 19115 RMVar_ID_19115 Human_SNP_ID_69016471 A-to-I Human chr2 + 42313066 42313066 42313066 CACCGCCTGCGTTCACGCCATTCTCCTGCCTCAGCCTTCCAAGTAGCTGGGACTACAGGCGCCTG CACCGCCTGCGTTCACGCCATTCTCCTGCCTCCGCCTTCCAAGTAGCTGGGACTACAGGCGCCTG A C EML4 Ensembl:ENSG00000143924 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1434926159 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56385,RMVar_hsa_circ_21554,RMVar_hsa_circ_56098,RMVar_hsa_circ_357628,RMVar_hsa_circ_14610,RMVar_hsa_circ_199240,RMVar_hsa_circ_126384,RMVar_hsa_circ_199241,RMVar_hsa_circ_357444,RMVar_hsa_circ_63929,RMVar_hsa_circ_61607,RMVar_hsa_circ_331583,RMVar_hsa_circ_312653,RMVar_hsa_circ_328416,RMVar_hsa_circ_49198,RMVar_hsa_circ_52739,RMVar_hsa_circ_199252,RMVar_hsa_circ_199251,RMVar_hsa_circ_118917,RMVar_hsa_circ_64669,RMVar_hsa_circ_290992,RMVar_hsa_circ_91940,RMVar_hsa_circ_199258,RMVar_hsa_circ_199259,RMVar_hsa_circ_199260 19116 RMVar_ID_19116 Human_SNP_ID_69016918 A-to-I Human chr2 + 42314428 42314428 42314428 TTCATGAATGAATTTTTAGTAACTTGTAAGCTATGGGCTGAAACTTTTAGGCAGCTAACCTAATT TTCATGAATGAATTTTTAGTAACTTGTAAGCTGTGGGCTGAAACTTTTAGGCAGCTAACCTAATT A G EML4 Ensembl:ENSG00000143924 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs548393725 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56385,RMVar_hsa_circ_21554,RMVar_hsa_circ_56098,RMVar_hsa_circ_357628,RMVar_hsa_circ_14610,RMVar_hsa_circ_199240,RMVar_hsa_circ_126384,RMVar_hsa_circ_199241,RMVar_hsa_circ_357444,RMVar_hsa_circ_63929,RMVar_hsa_circ_61607,RMVar_hsa_circ_331583,RMVar_hsa_circ_312653,RMVar_hsa_circ_328416,RMVar_hsa_circ_49198,RMVar_hsa_circ_52739,RMVar_hsa_circ_199252,RMVar_hsa_circ_199251,RMVar_hsa_circ_118917,RMVar_hsa_circ_64669,RMVar_hsa_circ_290992,RMVar_hsa_circ_91940,RMVar_hsa_circ_199258,RMVar_hsa_circ_199259,RMVar_hsa_circ_199260 19117 RMVar_ID_19117 Human_SNP_ID_69028373 A-to-I Human chr2 - 42352208 42352208 42352208 CTATGATTGAGCCACTGCATTCTAGCCTGGGTAGCAGAGTGAGACCCAGTCTCTAAAATGATGAT CTATGATTGAGCCACTGCATTCTAGCCTGGGTGGCAGAGTGAGACCCAGTCTCTAAAATGATGAT T C COX7A2L Ensembl:ENSG00000115944 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs954375971 Functional Loss SNV dbSNP153 33..33 33 - - - 19118 RMVar_ID_19118 Human_SNP_ID_69028384 A-to-I Human chr2 - 42352267 42352267 42352267 TACTCCAGAGGCCGAGGCGGGAGGATCACTTTAGCCCAGGATTTTGAGGTTGCAGTGAGCTATGA TACTCCAGAGGCCGAGGCGGGAGGATCACTTTGGCCCAGGATTTTGAGGTTGCAGTGAGCTATGA T C COX7A2L Ensembl:ENSG00000115944 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs535909732 Functional Loss SNV dbSNP153 33..33 33 - - - 19119 RMVar_ID_19119 Human_SNP_ID_69028414 A-to-I Human chr2 - 42352362 42352360 42352363 AGGAGGATTGCTTGATCAGCCTGGGCAGCATAACGAGACCCTGCCTCTACAAAAAAACTTAGCTG AGGAGGATTGCTTGATCAGCCTGGGCAGCAT___GAGACCCTGCCTCTACAAAAAAACTTAGCTG CGTT C COX7A2L Ensembl:ENSG00000115944 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1442799713 Functional Loss DEL dbSNP153 32..34 33 - - - 19120 RMVar_ID_19120 Human_SNP_ID_69028414 A-to-I Human chr2 - 42352363 42352360 42352363 TAGGAGGATTGCTTGATCAGCCTGGGCAGCATAACGAGACCCTGCCTCTACAAAAAAACTTAGCT TAGGAGGATTGCTTGATCAGCCTGGGCAGCAT___GAGACCCTGCCTCTACAAAAAAACTTAGCT CGTT C COX7A2L Ensembl:ENSG00000115944 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1442799713 Functional Loss DEL dbSNP153 33..35 33 - - - 19121 RMVar_ID_19121 Human_SNP_ID_69028422 A-to-I Human chr2 - 42352394 42352394 42352394 TGTGCAGCCCCAACACTTTGGGAGGCCAAGGTAGGAGGATTGCTTGATCAGCCTGGGCAGCATAA TGTGCAGCCCCAACACTTTGGGAGGCCAAGGTGGGAGGATTGCTTGATCAGCCTGGGCAGCATAA T C COX7A2L Ensembl:ENSG00000115944 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1371442331 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13888855 19122 RMVar_ID_19122 Human_SNP_ID_69028431 A-to-I Human chr2 - 42352414 42352414 42352414 GCCAGGTGTGGTGGCTCACTTGTGCAGCCCCAACACTTTGGGAGGCCAAGGTAGGAGGATTGCTT GCCAGGTGTGGTGGCTCACTTGTGCAGCCCCAGCACTTTGGGAGGCCAAGGTAGGAGGATTGCTT T C COX7A2L Ensembl:ENSG00000115944 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1391130995 Functional Loss SNV dbSNP153 33..33 33 - - - 19123 RMVar_ID_19123 Human_SNP_ID_69028436 A-to-I Human chr2 - 42352429 42352429 42352429 ATATGAGTTAAACAGGCCAGGTGTGGTGGCTCACTTGTGCAGCCCCAACACTTTGGGAGGCCAAG ATATGAGTTAAACAGGCCAGGTGTGGTGGCTCCCTTGTGCAGCCCCAACACTTTGGGAGGCCAAG T G COX7A2L Ensembl:ENSG00000115944 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1244726636 Functional Loss SNV dbSNP153 33..33 33 - - - 19124 RMVar_ID_19124 Human_SNP_ID_69029635 A-to-I Human chr2 - 42356743 42356743 42356743 TTTTTGATATTTTGTAGAAACAAGGTCTCACTACGTTGCCCAGGATGATCTCAAACTCCTGAGTC TTTTTGATATTTTGTAGAAACAAGGTCTCACTGCGTTGCCCAGGATGATCTCAAACTCCTGAGTC T C COX7A2L Ensembl:ENSG00000115944 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1314073538 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13888944 19125 RMVar_ID_19125 Human_SNP_ID_69029639 A-to-I Human chr2 - 42356760 42356760 42356760 CACTGTACCTGGCTAATTTTTTGATATTTTGTAGAAACAAGGTCTCACTACGTTGCCCAGGATGA CACTGTACCTGGCTAATTTTTTGATATTTTGTGGAAACAAGGTCTCACTACGTTGCCCAGGATGA T C COX7A2L Ensembl:ENSG00000115944 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs773823192 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13888944 19126 RMVar_ID_19126 Human_SNP_ID_69052629 A-to-I Human chr2 - 42437755 42437755 42437755 TTCTGTATTTTTAGTAGAGATGGGGTTTTGCCATGTTGGCCGGGCTGGTCTCGATCTCCTGACTT TTCTGTATTTTTAGTAGAGATGGGGTTTTGCCGTGTTGGCCGGGCTGGTCTCGATCTCCTGACTT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917527776 Functional Loss SNV dbSNP153 33..33 33 - - - 19127 RMVar_ID_19127 Human_SNP_ID_69099463 A-to-I Human chr2 + 42584787 42584787 42584787 TACTCAGGAGACTGAGGCAGGAGGATTGCTTGAGCCCAGGAGATTGAGGCTGCAGTGAGCTGTGT TACTCAGGAGACTGAGGCAGGAGGATTGCTTGCGCCCAGGAGATTGAGGCTGCAGTGAGCTGTGT A C MTA3 Ensembl:ENSG00000057935 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs188460344 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_365,RMVar_hsa_circ_199265,RMVar_hsa_circ_123561,RMVar_hsa_circ_113508,RMVar_hsa_circ_326740,RMVar_hsa_circ_347905,RMVar_hsa_circ_351096,RMVar_hsa_circ_49197,RMVar_hsa_circ_73274,RMVar_hsa_circ_199266,RMVar_hsa_circ_199267,RMVar_hsa_circ_104118,RMVar_hsa_circ_281776,RMVar_hsa_circ_21078,RMVar_hsa_circ_60702,RMVar_hsa_circ_199269 19128 RMVar_ID_19128 Human_SNP_ID_69099784 A-to-I Human chr2 + 42585614 42585614 42585614 CGCCTGCCTCAGCCTTCTGAGTAGCTGGAACTACAGATGTGTGCCACCACGCCTGGTTAATTTTT CGCCTGCCTCAGCCTTCTGAGTAGCTGGAACTGCAGATGTGTGCCACCACGCCTGGTTAATTTTT A G MTA3 Ensembl:ENSG00000057935 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1048760258 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_365,RMVar_hsa_circ_199265,RMVar_hsa_circ_123561,RMVar_hsa_circ_113508,RMVar_hsa_circ_326740,RMVar_hsa_circ_347905,RMVar_hsa_circ_351096,RMVar_hsa_circ_49197,RMVar_hsa_circ_73274,RMVar_hsa_circ_199266,RMVar_hsa_circ_199267,RMVar_hsa_circ_104118,RMVar_hsa_circ_281776,RMVar_hsa_circ_21078,RMVar_hsa_circ_60702,RMVar_hsa_circ_199269 19129 RMVar_ID_19129 Human_SNP_ID_69099787 A-to-I Human chr2 + 42585627 42585627 42585627 CTTCTGAGTAGCTGGAACTACAGATGTGTGCCACCACGCCTGGTTAATTTTTGTATTTTTATAGA CTTCTGAGTAGCTGGAACTACAGATGTGTGCCTCCACGCCTGGTTAATTTTTGTATTTTTATAGA A T MTA3 Ensembl:ENSG00000057935 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1315939051 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_365,RMVar_hsa_circ_199265,RMVar_hsa_circ_123561,RMVar_hsa_circ_113508,RMVar_hsa_circ_326740,RMVar_hsa_circ_347905,RMVar_hsa_circ_351096,RMVar_hsa_circ_49197,RMVar_hsa_circ_73274,RMVar_hsa_circ_199266,RMVar_hsa_circ_199267,RMVar_hsa_circ_104118,RMVar_hsa_circ_281776,RMVar_hsa_circ_21078,RMVar_hsa_circ_60702,RMVar_hsa_circ_199269 19130 RMVar_ID_19130 Human_SNP_ID_69099797 A-to-I Human chr2 + 42585657 42585657 42585657 CCACCACGCCTGGTTAATTTTTGTATTTTTATAGAGACCGGGTTTCACCGTGTTGGCCAGGATGG CCACCACGCCTGGTTAATTTTTGTATTTTTATGGAGACCGGGTTTCACCGTGTTGGCCAGGATGG A G MTA3 Ensembl:ENSG00000057935 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs906092966 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_365,RMVar_hsa_circ_199265,RMVar_hsa_circ_123561,RMVar_hsa_circ_113508,RMVar_hsa_circ_326740,RMVar_hsa_circ_347905,RMVar_hsa_circ_351096,RMVar_hsa_circ_49197,RMVar_hsa_circ_73274,RMVar_hsa_circ_199266,RMVar_hsa_circ_199267,RMVar_hsa_circ_104118,RMVar_hsa_circ_281776,RMVar_hsa_circ_21078,RMVar_hsa_circ_60702,RMVar_hsa_circ_199269 19131 RMVar_ID_19131 Human_SNP_ID_69104742 A-to-I Human chr2 + 42600674 42600674 42600674 AGCGATTCTTGTGCCTCAGTCTCCTAGTAGCTAGGATTACAGGGATGCGCCACCACACCTGGCTG AGCGATTCTTGTGCCTCAGTCTCCTAGTAGCTGGGATTACAGGGATGCGCCACCACACCTGGCTG A G MTA3 Ensembl:ENSG00000057935 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1558481212 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_365,RMVar_hsa_circ_199265,RMVar_hsa_circ_123561,RMVar_hsa_circ_113508,RMVar_hsa_circ_326740,RMVar_hsa_circ_347905,RMVar_hsa_circ_351096,RMVar_hsa_circ_49197,RMVar_hsa_circ_73274,RMVar_hsa_circ_199266,RMVar_hsa_circ_199267,RMVar_hsa_circ_104118,RMVar_hsa_circ_281776,RMVar_hsa_circ_21078,RMVar_hsa_circ_60702,RMVar_hsa_circ_199269 19132 RMVar_ID_19132 Human_SNP_ID_69109742 A-to-I Human chr2 + 42614836 42614836 42614836 GTCTCTATAAATAATAAAAAAATTAGCATGGCATGGCAGCGTATGCCTGTATTCCCAGAAGTATT GTCTCTATAAATAATAAAAAAATTAGCATGGCGTGGCAGCGTATGCCTGTATTCCCAGAAGTATT A G MTA3 Ensembl:ENSG00000057935 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1347034160 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_365,RMVar_hsa_circ_199265,RMVar_hsa_circ_123561,RMVar_hsa_circ_113508,RMVar_hsa_circ_347905,RMVar_hsa_circ_351096,RMVar_hsa_circ_49197,RMVar_hsa_circ_47461,RMVar_hsa_circ_73274,RMVar_hsa_circ_199266,RMVar_hsa_circ_104118,RMVar_hsa_circ_21078,RMVar_hsa_circ_60702,RMVar_hsa_circ_199269,RMVar_hsa_circ_377906,RMVar_hsa_circ_59450,RMVar_hsa_circ_4622,RMVar_hsa_circ_199271,RMVar_hsa_circ_199272 19133 RMVar_ID_19133 Human_SNP_ID_69109757 A-to-I Human chr2 + 42614902 42614902 42614902 GGGAAGTTGAGGTAGGAGGATTGCTTGAGCCCAGGAGTTCAAGGCTATAGTGAGCCATGATTGTG GGGAAGTTGAGGTAGGAGGATTGCTTGAGCCCGGGAGTTCAAGGCTATAGTGAGCCATGATTGTG A G MTA3 Ensembl:ENSG00000057935 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs757415614 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_365,RMVar_hsa_circ_199265,RMVar_hsa_circ_123561,RMVar_hsa_circ_113508,RMVar_hsa_circ_347905,RMVar_hsa_circ_351096,RMVar_hsa_circ_49197,RMVar_hsa_circ_47461,RMVar_hsa_circ_73274,RMVar_hsa_circ_199266,RMVar_hsa_circ_104118,RMVar_hsa_circ_21078,RMVar_hsa_circ_60702,RMVar_hsa_circ_199269,RMVar_hsa_circ_377906,RMVar_hsa_circ_59450,RMVar_hsa_circ_4622,RMVar_hsa_circ_199271,RMVar_hsa_circ_199272 19134 RMVar_ID_19134 Human_SNP_ID_69109764 A-to-I Human chr2 + 42614916 42614916 42614916 GGAGGATTGCTTGAGCCCAGGAGTTCAAGGCTATAGTGAGCCATGATTGTGACACTGTACTTTAG GGAGGATTGCTTGAGCCCAGGAGTTCAAGGCTGTAGTGAGCCATGATTGTGACACTGTACTTTAG A G MTA3 Ensembl:ENSG00000057935 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs115584508 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_365,RMVar_hsa_circ_199265,RMVar_hsa_circ_123561,RMVar_hsa_circ_113508,RMVar_hsa_circ_347905,RMVar_hsa_circ_351096,RMVar_hsa_circ_49197,RMVar_hsa_circ_47461,RMVar_hsa_circ_73274,RMVar_hsa_circ_199266,RMVar_hsa_circ_104118,RMVar_hsa_circ_21078,RMVar_hsa_circ_60702,RMVar_hsa_circ_199269,RMVar_hsa_circ_377906,RMVar_hsa_circ_59450,RMVar_hsa_circ_4622,RMVar_hsa_circ_199271,RMVar_hsa_circ_199272 19135 RMVar_ID_19135 Human_SNP_ID_69116780 A-to-I Human chr2 + 42635859 42635859 42635859 CATGATCTTGGCTCACTGCACCTCCTTCTCCCAGGTTCAAGCAGTTCTTGTGCCACAGCCTCCGC CATGATCTTGGCTCACTGCACCTCCTTCTCCCGGGTTCAAGCAGTTCTTGTGCCACAGCCTCCGC A G MTA3 Ensembl:ENSG00000057935 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1035642340 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_365,RMVar_hsa_circ_199265,RMVar_hsa_circ_123561,RMVar_hsa_circ_113508,RMVar_hsa_circ_347905,RMVar_hsa_circ_351096,RMVar_hsa_circ_49197,RMVar_hsa_circ_47461,RMVar_hsa_circ_73274,RMVar_hsa_circ_199266,RMVar_hsa_circ_104118,RMVar_hsa_circ_21078,RMVar_hsa_circ_60702,RMVar_hsa_circ_199269,RMVar_hsa_circ_377906,RMVar_hsa_circ_59450,RMVar_hsa_circ_4622,RMVar_hsa_circ_199271,RMVar_hsa_circ_199272 19136 RMVar_ID_19136 Human_SNP_ID_69121591 A-to-I Human chr2 + 42651516 42651516 42651516 GTTACCAAAAGAATAGGCAATTGGTGCTGGGCATGGTGGCTCATGCTTGTAATCCCAGTGCTTAG GTTACCAAAAGAATAGGCAATTGGTGCTGGGCCTGGTGGCTCATGCTTGTAATCCCAGTGCTTAG A C MTA3 Ensembl:ENSG00000057935 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs568378197 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_365,RMVar_hsa_circ_199265,RMVar_hsa_circ_123561,RMVar_hsa_circ_113508,RMVar_hsa_circ_351096,RMVar_hsa_circ_49197,RMVar_hsa_circ_12585,RMVar_hsa_circ_47461,RMVar_hsa_circ_199266,RMVar_hsa_circ_104118,RMVar_hsa_circ_21078,RMVar_hsa_circ_60702,RMVar_hsa_circ_199269,RMVar_hsa_circ_377906,RMVar_hsa_circ_59450,RMVar_hsa_circ_270383,RMVar_hsa_circ_199271,RMVar_hsa_circ_357251,RMVar_hsa_circ_366146,RMVar_hsa_circ_289856,RMVar_hsa_circ_108363,RMVar_hsa_circ_117720,RMVar_hsa_circ_71354,RMVar_hsa_circ_199273,RMVar_hsa_circ_199274,RMVar_hsa_circ_199275,RMVar_hsa_circ_97193,RMVar_hsa_circ_199276 19137 RMVar_ID_19137 Human_SNP_ID_69121592 A-to-I Human chr2 + 42651516 42651516 42651516 GTTACCAAAAGAATAGGCAATTGGTGCTGGGCATGGTGGCTCATGCTTGTAATCCCAGTGCTTAG GTTACCAAAAGAATAGGCAATTGGTGCTGGGCGTGGTGGCTCATGCTTGTAATCCCAGTGCTTAG A G MTA3 Ensembl:ENSG00000057935 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs568378197 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_365,RMVar_hsa_circ_199265,RMVar_hsa_circ_123561,RMVar_hsa_circ_113508,RMVar_hsa_circ_351096,RMVar_hsa_circ_49197,RMVar_hsa_circ_12585,RMVar_hsa_circ_47461,RMVar_hsa_circ_199266,RMVar_hsa_circ_104118,RMVar_hsa_circ_21078,RMVar_hsa_circ_60702,RMVar_hsa_circ_199269,RMVar_hsa_circ_377906,RMVar_hsa_circ_59450,RMVar_hsa_circ_270383,RMVar_hsa_circ_199271,RMVar_hsa_circ_357251,RMVar_hsa_circ_366146,RMVar_hsa_circ_289856,RMVar_hsa_circ_108363,RMVar_hsa_circ_117720,RMVar_hsa_circ_71354,RMVar_hsa_circ_199273,RMVar_hsa_circ_199274,RMVar_hsa_circ_199275,RMVar_hsa_circ_97193,RMVar_hsa_circ_199276 19138 RMVar_ID_19138 Human_SNP_ID_69121593 A-to-I Human chr2 + 42651516 42651516 42651516 GTTACCAAAAGAATAGGCAATTGGTGCTGGGCATGGTGGCTCATGCTTGTAATCCCAGTGCTTAG GTTACCAAAAGAATAGGCAATTGGTGCTGGGCTTGGTGGCTCATGCTTGTAATCCCAGTGCTTAG A T MTA3 Ensembl:ENSG00000057935 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs568378197 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_365,RMVar_hsa_circ_199265,RMVar_hsa_circ_123561,RMVar_hsa_circ_113508,RMVar_hsa_circ_351096,RMVar_hsa_circ_49197,RMVar_hsa_circ_12585,RMVar_hsa_circ_47461,RMVar_hsa_circ_199266,RMVar_hsa_circ_104118,RMVar_hsa_circ_21078,RMVar_hsa_circ_60702,RMVar_hsa_circ_199269,RMVar_hsa_circ_377906,RMVar_hsa_circ_59450,RMVar_hsa_circ_270383,RMVar_hsa_circ_199271,RMVar_hsa_circ_357251,RMVar_hsa_circ_366146,RMVar_hsa_circ_289856,RMVar_hsa_circ_108363,RMVar_hsa_circ_117720,RMVar_hsa_circ_71354,RMVar_hsa_circ_199273,RMVar_hsa_circ_199274,RMVar_hsa_circ_199275,RMVar_hsa_circ_97193,RMVar_hsa_circ_199276 19139 RMVar_ID_19139 Human_SNP_ID_69136472 A-to-I Human chr2 + 42703152 42703151 42703153 TGGGTAATTTTTATTTTTGTTTTTGTAGAGACAGAGTCTCACTGTGTTGCCCAGGCTGGTCTCCG TGGGTAATTTTTATTTTTGTTTTTGTAGAGAC__AGTCTCACTGTGTTGCCCAGGCTGGTCTCCG CAG C MTA3 Ensembl:ENSG00000057935 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs747455849 Functional Loss DEL dbSNP153 33..34 33 - - - 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 19140 RMVar_ID_19140 Human_SNP_ID_69159920 A-to-I Human chr2 - 42781676 42781676 42781676 TAGAAATTGGGTTTCACCATGTTGGCCAGGCTAGTCTCGAACTCCTGACCTCAGGTGACCCATCT TAGAAATTGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAGGTGACCCATCT T C HAAO Ensembl:ENSG00000162882 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1280093286 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104116,RMVar_hsa_circ_71184,RMVar_hsa_circ_106859,RMVar_hsa_circ_199304,RMVar_hsa_circ_199306,RMVar_hsa_circ_87194,RMVar_hsa_circ_199305 19141 RMVar_ID_19141 Human_SNP_ID_69159940 A-to-I Human chr2 - 42781752 42781752 42781752 CTCCTGCCTTAACTTCTTGAGTAGTTGGGATTACAGGCACCCGCCACCACACCCGGCTAATTTTT CTCCTGCCTTAACTTCTTGAGTAGTTGGGATTGCAGGCACCCGCCACCACACCCGGCTAATTTTT T C HAAO Ensembl:ENSG00000162882 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs982279076 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104116,RMVar_hsa_circ_71184,RMVar_hsa_circ_106859,RMVar_hsa_circ_199304,RMVar_hsa_circ_199306,RMVar_hsa_circ_87194,RMVar_hsa_circ_199305 19142 RMVar_ID_19142 Human_SNP_ID_69297985 A-to-I Human chr2 - 43234770 43234770 43234770 CACATGCCTATAGTCCCAGCTACTTGGGGGCTAAGGCAGGAGAATTGCTTGAACCCAGGAGGCGG CACATGCCTATAGTCCCAGCTACTTGGGGGCTGAGGCAGGAGAATTGCTTGAACCCAGGAGGCGG T C THADA Ensembl:ENSG00000115970 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1490740573 Functional Loss SNV dbSNP153 33..33 33 - - - 19143 RMVar_ID_19143 Human_SNP_ID_69325318 A-to-I Human chr2 - 43332223 43332223 43332223 TTAATTTTTTAGCATGGTGGCATGGGCCTGTAATCCCAGCTTCTTGGGAGGCTGAGGCACAAGAA TTAATTTTTTAGCATGGTGGCATGGGCCTGTAGTCCCAGCTTCTTGGGAGGCTGAGGCACAAGAA T C THADA Ensembl:ENSG00000115970 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1322769534 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95797,RMVar_hsa_circ_199310,RMVar_hsa_circ_87506,RMVar_hsa_circ_199315,RMVar_hsa_circ_199316,RMVar_hsa_circ_29454,RMVar_hsa_circ_296613,RMVar_hsa_circ_319802,RMVar_hsa_circ_85538,RMVar_hsa_circ_199317,RMVar_hsa_circ_199318 19144 RMVar_ID_19144 Human_SNP_ID_69350215 A-to-I Human chr2 - 43425252 43425252 43425252 GTCTTTCTGCCAAGTATTGAACTGGTCATTTTACTTACAGTGACTCTGAGAAGAGGTGTTATCAC GTCTTTCTGCCAAGTATTGAACTGGTCATTTTGCTTACAGTGACTCTGAGAAGAGGTGTTATCAC T C THADA Ensembl:ENSG00000115970 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs966660218 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95797,RMVar_hsa_circ_199310,RMVar_hsa_circ_87506,RMVar_hsa_circ_199315,RMVar_hsa_circ_116731,RMVar_hsa_circ_29454,RMVar_hsa_circ_85538,RMVar_hsa_circ_199318,RMVar_hsa_circ_355755,RMVar_hsa_circ_67821,RMVar_hsa_circ_357530,RMVar_hsa_circ_374635,RMVar_hsa_circ_39827,RMVar_hsa_circ_373871,RMVar_hsa_circ_320189,RMVar_hsa_circ_345174,RMVar_hsa_circ_319419,RMVar_hsa_circ_125071,RMVar_hsa_circ_272298,RMVar_hsa_circ_119645,RMVar_hsa_circ_199320,RMVar_hsa_circ_199322,RMVar_hsa_circ_199324,RMVar_hsa_circ_199326,RMVar_hsa_circ_199325,RMVar_hsa_circ_199323,RMVar_hsa_circ_199321 19145 RMVar_ID_19145 Human_SNP_ID_69388221 A-to-I Human chr2 - 43551889 43551889 43551889 CTGCAGTTGGTGAGCGAGTGGAGACCTGTGGTAGAGAAGCTCCTTTTGATGTCCTACAGGCTTTC CTGCAGTTGGTGAGCGAGTGGAGACCTGTGGTGGAGAAGCTCCTTTTGATGTCCTACAGGCTTTC T C THADA Ensembl:ENSG00000115970 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1336453574 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1067907,Human_RBP_ID_5527562,Human_RBP_ID_18999351,Human_RBP_ID_25574785 Human_Splice_Rec_239894,Human_Splice_Rec_239942,Human_Splice_Rec_240010,Human_Splice_Rec_240082,Human_Splice_Rec_240172,Human_Splice_Rec_240210 RMVar_hsa_circ_95797,RMVar_hsa_circ_199310,RMVar_hsa_circ_3302,RMVar_hsa_circ_20101,RMVar_hsa_circ_116731,RMVar_hsa_circ_85538,RMVar_hsa_circ_199318,RMVar_hsa_circ_67821,RMVar_hsa_circ_125071,RMVar_hsa_circ_199320,RMVar_hsa_circ_199321,RMVar_hsa_circ_94056,RMVar_hsa_circ_98536,RMVar_hsa_circ_77972,RMVar_hsa_circ_73761,RMVar_hsa_circ_199331,RMVar_hsa_circ_199332,RMVar_hsa_circ_199333,RMVar_hsa_circ_353419,RMVar_hsa_circ_354091,RMVar_hsa_circ_102623,RMVar_hsa_circ_20550,RMVar_hsa_circ_65548,RMVar_hsa_circ_199336,RMVar_hsa_circ_2129,RMVar_hsa_circ_363610,RMVar_hsa_circ_348178,RMVar_hsa_circ_18137,RMVar_hsa_circ_10104,RMVar_hsa_circ_66819,RMVar_hsa_circ_88078,RMVar_hsa_circ_199339,RMVar_hsa_circ_32868,RMVar_hsa_circ_77942,RMVar_hsa_circ_199340,RMVar_hsa_circ_11370,RMVar_hsa_circ_266600,RMVar_hsa_circ_12285,RMVar_hsa_circ_199341,RMVar_hsa_circ_327401,RMVar_hsa_circ_363970,RMVar_hsa_circ_373825,RMVar_hsa_circ_326139,RMVar_hsa_circ_64773,RMVar_hsa_circ_72950,RMVar_hsa_circ_59174,RMVar_hsa_circ_199342 19146 RMVar_ID_19146 Human_SNP_ID_69389807 A-to-I Human chr2 - 43557342 43557342 43557342 AGAGACTATGAACTGCCCTGTCTAGAAATAGTAAAGATAGTCTGGCTGTAGTCATAGCAAAATTC AGAGACTATGAACTGCCCTGTCTAGAAATAGTGAAGATAGTCTGGCTGTAGTCATAGCAAAATTC T C THADA Ensembl:ENSG00000115970 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1035115982 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13890706 RMVar_hsa_circ_95797,RMVar_hsa_circ_199310,RMVar_hsa_circ_3302,RMVar_hsa_circ_20101,RMVar_hsa_circ_116731,RMVar_hsa_circ_85538,RMVar_hsa_circ_199318,RMVar_hsa_circ_67821,RMVar_hsa_circ_125071,RMVar_hsa_circ_199320,RMVar_hsa_circ_199321,RMVar_hsa_circ_98536,RMVar_hsa_circ_73761,RMVar_hsa_circ_199333,RMVar_hsa_circ_354091,RMVar_hsa_circ_20550,RMVar_hsa_circ_65548,RMVar_hsa_circ_2129,RMVar_hsa_circ_363610,RMVar_hsa_circ_18137,RMVar_hsa_circ_10104,RMVar_hsa_circ_88078,RMVar_hsa_circ_199340,RMVar_hsa_circ_11370,RMVar_hsa_circ_14325,RMVar_hsa_circ_266600,RMVar_hsa_circ_12285,RMVar_hsa_circ_327401,RMVar_hsa_circ_363970,RMVar_hsa_circ_326139,RMVar_hsa_circ_64773,RMVar_hsa_circ_72950,RMVar_hsa_circ_59174,RMVar_hsa_circ_42609,RMVar_hsa_circ_94216,RMVar_hsa_circ_107013,RMVar_hsa_circ_44362,RMVar_hsa_circ_199344,RMVar_hsa_circ_199345 19147 RMVar_ID_19147 Human_SNP_ID_69393826 A-to-I Human chr2 - 43571132 43571130 43571132 TCCTCCCCAGCCTCTGAAGTAGCTGGGATGACAGGGGCACACCACCATGCCTGACTAATATTTAA TCCTCCCCAGCCTCTGAAGTAGCTGGGATGAC__GGGCACACCACCATGCCTGACTAATATTTAA CCT C THADA Ensembl:ENSG00000115970 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277882887 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_95797,RMVar_hsa_circ_199310,RMVar_hsa_circ_116731,RMVar_hsa_circ_85538,RMVar_hsa_circ_199318,RMVar_hsa_circ_67821,RMVar_hsa_circ_125071,RMVar_hsa_circ_199320,RMVar_hsa_circ_199321,RMVar_hsa_circ_98536,RMVar_hsa_circ_73761,RMVar_hsa_circ_199333,RMVar_hsa_circ_354091,RMVar_hsa_circ_20550,RMVar_hsa_circ_2129,RMVar_hsa_circ_363610,RMVar_hsa_circ_18137,RMVar_hsa_circ_88078,RMVar_hsa_circ_199340,RMVar_hsa_circ_11370,RMVar_hsa_circ_12937,RMVar_hsa_circ_14325,RMVar_hsa_circ_266600,RMVar_hsa_circ_363970,RMVar_hsa_circ_64773,RMVar_hsa_circ_72950,RMVar_hsa_circ_59174,RMVar_hsa_circ_42609,RMVar_hsa_circ_94216,RMVar_hsa_circ_107013,RMVar_hsa_circ_44362,RMVar_hsa_circ_199344,RMVar_hsa_circ_199345,RMVar_hsa_circ_38446,RMVar_hsa_circ_46388,RMVar_hsa_circ_267665,RMVar_hsa_circ_357379,RMVar_hsa_circ_31181,RMVar_hsa_circ_353147,RMVar_hsa_circ_19807,RMVar_hsa_circ_30264,RMVar_hsa_circ_350252 19148 RMVar_ID_19148 Human_SNP_ID_69393827 A-to-I Human chr2 - 43571132 43571132 43571132 TCCTCCCCAGCCTCTGAAGTAGCTGGGATGACAGGGGCACACCACCATGCCTGACTAATATTTAA TCCTCCCCAGCCTCTGAAGTAGCTGGGATGACGGGGGCACACCACCATGCCTGACTAATATTTAA T C THADA Ensembl:ENSG00000115970 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1439676938 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95797,RMVar_hsa_circ_199310,RMVar_hsa_circ_116731,RMVar_hsa_circ_85538,RMVar_hsa_circ_199318,RMVar_hsa_circ_67821,RMVar_hsa_circ_125071,RMVar_hsa_circ_199320,RMVar_hsa_circ_199321,RMVar_hsa_circ_98536,RMVar_hsa_circ_73761,RMVar_hsa_circ_199333,RMVar_hsa_circ_354091,RMVar_hsa_circ_20550,RMVar_hsa_circ_2129,RMVar_hsa_circ_363610,RMVar_hsa_circ_18137,RMVar_hsa_circ_88078,RMVar_hsa_circ_199340,RMVar_hsa_circ_11370,RMVar_hsa_circ_12937,RMVar_hsa_circ_14325,RMVar_hsa_circ_266600,RMVar_hsa_circ_363970,RMVar_hsa_circ_64773,RMVar_hsa_circ_72950,RMVar_hsa_circ_59174,RMVar_hsa_circ_42609,RMVar_hsa_circ_94216,RMVar_hsa_circ_107013,RMVar_hsa_circ_44362,RMVar_hsa_circ_199344,RMVar_hsa_circ_199345,RMVar_hsa_circ_38446,RMVar_hsa_circ_46388,RMVar_hsa_circ_267665,RMVar_hsa_circ_357379,RMVar_hsa_circ_31181,RMVar_hsa_circ_353147,RMVar_hsa_circ_19807,RMVar_hsa_circ_30264,RMVar_hsa_circ_350252 19149 RMVar_ID_19149 Human_SNP_ID_69455244 A-to-I Human chr2 + 43774095 43774095 43774095 TGCGGAGCTCGCCGCCTGATTCTAGGCTGGTCACTACTCCGAGCCTGTGACGTTTGCGGCAGCCA TGCGGAGCTCGCCGCCTGATTCTAGGCTGGTCGCTACTCCGAGCCTGTGACGTTTGCGGCAGCCA A G DYNC2LI1 Ensembl:ENSG00000138036 Protein coding 5'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1234272921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_551204,Human_RBP_ID_4623264 Human_Splice_Rec_240569,Human_Splice_Rec_240593,Human_Splice_Rec_240603,Human_Splice_Rec_240613,Human_Splice_Rec_240623,Human_Splice_Rec_240645,Human_Splice_Rec_240669 19150 RMVar_ID_19150 Human_SNP_ID_69460817 A-to-I Human chr2 + 43793715 43793714 43793716 CTCCTGCCTCAGCTTCCCAAAGCTCTAGAATTACAGACATGAGCCACCATCCCTGGCCTCTTTGC CTCCTGCCTCAGCTTCCCAAAGCTCTAGAATT__AGACATGAGCCACCATCCCTGGCCTCTTTGC TAC T DYNC2LI1 Ensembl:ENSG00000138036 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1211937270 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_23872751 RMVar_hsa_circ_7342,RMVar_hsa_circ_338020,RMVar_hsa_circ_306602,RMVar_hsa_circ_1302,RMVar_hsa_circ_17523,RMVar_hsa_circ_376726,RMVar_hsa_circ_199369,RMVar_hsa_circ_24300 19151 RMVar_ID_19151 Human_SNP_ID_69460818 A-to-I Human chr2 + 43793715 43793715 43793715 CTCCTGCCTCAGCTTCCCAAAGCTCTAGAATTACAGACATGAGCCACCATCCCTGGCCTCTTTGC CTCCTGCCTCAGCTTCCCAAAGCTCTAGAATTGCAGACATGAGCCACCATCCCTGGCCTCTTTGC A G DYNC2LI1 Ensembl:ENSG00000138036 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054376240 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23872751 RMVar_hsa_circ_7342,RMVar_hsa_circ_338020,RMVar_hsa_circ_306602,RMVar_hsa_circ_1302,RMVar_hsa_circ_17523,RMVar_hsa_circ_376726,RMVar_hsa_circ_199369,RMVar_hsa_circ_24300 19152 RMVar_ID_19152 Human_SNP_ID_69500840 A-to-I Human chr2 - 43915536 43915536 43915536 GGGACTACAGGCGCACACCACCACGCCCGGCTAGTTTTTGTATTTTTAGTAGAGACAGGGTTTCC GGGACTACAGGCGCACACCACCACGCCCGGCTCGTTTTTGTATTTTTAGTAGAGACAGGGTTTCC T G LRPPRC Ensembl:ENSG00000138095 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1486745450 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_628,RMVar_hsa_circ_23322,RMVar_hsa_circ_57044,RMVar_hsa_circ_267196,RMVar_hsa_circ_377576,RMVar_hsa_circ_42731,RMVar_hsa_circ_33116,RMVar_hsa_circ_121609,RMVar_hsa_circ_334855,RMVar_hsa_circ_321566,RMVar_hsa_circ_56178,RMVar_hsa_circ_308772,RMVar_hsa_circ_199381,RMVar_hsa_circ_199382,RMVar_hsa_circ_59979,RMVar_hsa_circ_34062,RMVar_hsa_circ_305149,RMVar_hsa_circ_199383,RMVar_hsa_circ_25563,RMVar_hsa_circ_335353,RMVar_hsa_circ_341074,RMVar_hsa_circ_365415,RMVar_hsa_circ_313240,RMVar_hsa_circ_65860,RMVar_hsa_circ_78179,RMVar_hsa_circ_42425,RMVar_hsa_circ_199391,RMVar_hsa_circ_340645,RMVar_hsa_circ_114021,RMVar_hsa_circ_199385,RMVar_hsa_circ_199387,RMVar_hsa_circ_199388,RMVar_hsa_circ_199386,RMVar_hsa_circ_199384,RMVar_hsa_circ_268053,RMVar_hsa_circ_355943,RMVar_hsa_circ_373562,RMVar_hsa_circ_375386,RMVar_hsa_circ_199389,RMVar_hsa_circ_374357,RMVar_hsa_circ_368467,RMVar_hsa_circ_342103,RMVar_hsa_circ_21576,RMVar_hsa_circ_291441,RMVar_hsa_circ_273864,RMVar_hsa_circ_199393,RMVar_hsa_circ_199395,RMVar_hsa_circ_199396,RMVar_hsa_circ_199394,RMVar_hsa_circ_199392,RMVar_hsa_circ_19510,RMVar_hsa_circ_283018,RMVar_hsa_circ_341842,RMVar_hsa_circ_352126,RMVar_hsa_circ_199390,RMVar_hsa_circ_361710,RMVar_hsa_circ_344611,RMVar_hsa_circ_305321,RMVar_hsa_circ_57799,RMVar_hsa_circ_275221,RMVar_hsa_circ_38372,RMVar_hsa_circ_199398,RMVar_hsa_circ_199399,RMVar_hsa_circ_199397 19153 RMVar_ID_19153 Human_SNP_ID_69500988 A-to-I Human chr2 - 43916060 43916060 43916060 TTAATTTCCTAACTTAACTAGAAGGTTTGGCCAGGCTTGCAGGCTCATGCCTATAATCCCAACAA TTAATTTCCTAACTTAACTAGAAGGTTTGGCCGGGCTTGCAGGCTCATGCCTATAATCCCAACAA T C LRPPRC Ensembl:ENSG00000138095 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs947227257 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13892201,Human_RBP_ID_23872871 RMVar_hsa_circ_628,RMVar_hsa_circ_23322,RMVar_hsa_circ_57044,RMVar_hsa_circ_267196,RMVar_hsa_circ_377576,RMVar_hsa_circ_42731,RMVar_hsa_circ_33116,RMVar_hsa_circ_121609,RMVar_hsa_circ_334855,RMVar_hsa_circ_321566,RMVar_hsa_circ_56178,RMVar_hsa_circ_308772,RMVar_hsa_circ_199381,RMVar_hsa_circ_199382,RMVar_hsa_circ_59979,RMVar_hsa_circ_34062,RMVar_hsa_circ_305149,RMVar_hsa_circ_199383,RMVar_hsa_circ_25563,RMVar_hsa_circ_335353,RMVar_hsa_circ_341074,RMVar_hsa_circ_365415,RMVar_hsa_circ_313240,RMVar_hsa_circ_65860,RMVar_hsa_circ_78179,RMVar_hsa_circ_42425,RMVar_hsa_circ_199391,RMVar_hsa_circ_340645,RMVar_hsa_circ_114021,RMVar_hsa_circ_199385,RMVar_hsa_circ_199387,RMVar_hsa_circ_199388,RMVar_hsa_circ_199386,RMVar_hsa_circ_199384,RMVar_hsa_circ_268053,RMVar_hsa_circ_355943,RMVar_hsa_circ_373562,RMVar_hsa_circ_375386,RMVar_hsa_circ_199389,RMVar_hsa_circ_374357,RMVar_hsa_circ_368467,RMVar_hsa_circ_342103,RMVar_hsa_circ_21576,RMVar_hsa_circ_291441,RMVar_hsa_circ_273864,RMVar_hsa_circ_199393,RMVar_hsa_circ_199395,RMVar_hsa_circ_199396,RMVar_hsa_circ_199394,RMVar_hsa_circ_199392,RMVar_hsa_circ_19510,RMVar_hsa_circ_283018,RMVar_hsa_circ_341842,RMVar_hsa_circ_352126,RMVar_hsa_circ_199390,RMVar_hsa_circ_361710,RMVar_hsa_circ_344611,RMVar_hsa_circ_305321,RMVar_hsa_circ_57799,RMVar_hsa_circ_275221,RMVar_hsa_circ_38372,RMVar_hsa_circ_199398,RMVar_hsa_circ_199399,RMVar_hsa_circ_199397 19154 RMVar_ID_19154 Human_SNP_ID_69501362 A-to-I Human chr2 - 43917244 43917244 43917244 ACGAAGTCAAGAGATGGAGACCATCCTGGCCAACATGGTGAAACTCCATCTCTACTAGAAATACC ACGAAGTCAAGAGATGGAGACCATCCTGGCCAGCATGGTGAAACTCCATCTCTACTAGAAATACC T C LRPPRC Ensembl:ENSG00000138095 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs542775558 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_628,RMVar_hsa_circ_23322,RMVar_hsa_circ_57044,RMVar_hsa_circ_267196,RMVar_hsa_circ_377576,RMVar_hsa_circ_42731,RMVar_hsa_circ_33116,RMVar_hsa_circ_121609,RMVar_hsa_circ_334855,RMVar_hsa_circ_321566,RMVar_hsa_circ_56178,RMVar_hsa_circ_308772,RMVar_hsa_circ_199381,RMVar_hsa_circ_199382,RMVar_hsa_circ_59979,RMVar_hsa_circ_34062,RMVar_hsa_circ_305149,RMVar_hsa_circ_199383,RMVar_hsa_circ_25563,RMVar_hsa_circ_335353,RMVar_hsa_circ_341074,RMVar_hsa_circ_365415,RMVar_hsa_circ_313240,RMVar_hsa_circ_65860,RMVar_hsa_circ_78179,RMVar_hsa_circ_42425,RMVar_hsa_circ_199391,RMVar_hsa_circ_340645,RMVar_hsa_circ_114021,RMVar_hsa_circ_199385,RMVar_hsa_circ_199387,RMVar_hsa_circ_199388,RMVar_hsa_circ_199386,RMVar_hsa_circ_199384,RMVar_hsa_circ_268053,RMVar_hsa_circ_355943,RMVar_hsa_circ_373562,RMVar_hsa_circ_375386,RMVar_hsa_circ_199389,RMVar_hsa_circ_374357,RMVar_hsa_circ_368467,RMVar_hsa_circ_342103,RMVar_hsa_circ_21576,RMVar_hsa_circ_291441,RMVar_hsa_circ_273864,RMVar_hsa_circ_199393,RMVar_hsa_circ_199395,RMVar_hsa_circ_199396,RMVar_hsa_circ_199394,RMVar_hsa_circ_199392,RMVar_hsa_circ_19510,RMVar_hsa_circ_283018,RMVar_hsa_circ_341842,RMVar_hsa_circ_352126,RMVar_hsa_circ_199390,RMVar_hsa_circ_361710,RMVar_hsa_circ_344611,RMVar_hsa_circ_305321,RMVar_hsa_circ_57799,RMVar_hsa_circ_275221,RMVar_hsa_circ_38372,RMVar_hsa_circ_199398,RMVar_hsa_circ_199399,RMVar_hsa_circ_199397 19155 RMVar_ID_19155 Human_SNP_ID_69501369 A-to-I Human chr2 - 43917267 43917267 43917267 CAGCCTCCCAAAGCTGGCAGATCACGAAGTCAAGAGATGGAGACCATCCTGGCCAACATGGTGAA CAGCCTCCCAAAGCTGGCAGATCACGAAGTCAGGAGATGGAGACCATCCTGGCCAACATGGTGAA T C LRPPRC Ensembl:ENSG00000138095 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1281369754 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_628,RMVar_hsa_circ_23322,RMVar_hsa_circ_57044,RMVar_hsa_circ_267196,RMVar_hsa_circ_377576,RMVar_hsa_circ_42731,RMVar_hsa_circ_33116,RMVar_hsa_circ_121609,RMVar_hsa_circ_334855,RMVar_hsa_circ_321566,RMVar_hsa_circ_56178,RMVar_hsa_circ_308772,RMVar_hsa_circ_199381,RMVar_hsa_circ_199382,RMVar_hsa_circ_59979,RMVar_hsa_circ_34062,RMVar_hsa_circ_305149,RMVar_hsa_circ_199383,RMVar_hsa_circ_25563,RMVar_hsa_circ_335353,RMVar_hsa_circ_341074,RMVar_hsa_circ_365415,RMVar_hsa_circ_313240,RMVar_hsa_circ_65860,RMVar_hsa_circ_78179,RMVar_hsa_circ_42425,RMVar_hsa_circ_199391,RMVar_hsa_circ_340645,RMVar_hsa_circ_114021,RMVar_hsa_circ_199385,RMVar_hsa_circ_199387,RMVar_hsa_circ_199388,RMVar_hsa_circ_199386,RMVar_hsa_circ_199384,RMVar_hsa_circ_268053,RMVar_hsa_circ_355943,RMVar_hsa_circ_373562,RMVar_hsa_circ_375386,RMVar_hsa_circ_199389,RMVar_hsa_circ_374357,RMVar_hsa_circ_368467,RMVar_hsa_circ_342103,RMVar_hsa_circ_21576,RMVar_hsa_circ_291441,RMVar_hsa_circ_273864,RMVar_hsa_circ_199393,RMVar_hsa_circ_199395,RMVar_hsa_circ_199396,RMVar_hsa_circ_199394,RMVar_hsa_circ_199392,RMVar_hsa_circ_19510,RMVar_hsa_circ_283018,RMVar_hsa_circ_341842,RMVar_hsa_circ_352126,RMVar_hsa_circ_199390,RMVar_hsa_circ_361710,RMVar_hsa_circ_344611,RMVar_hsa_circ_305321,RMVar_hsa_circ_57799,RMVar_hsa_circ_275221,RMVar_hsa_circ_38372,RMVar_hsa_circ_199398,RMVar_hsa_circ_199399,RMVar_hsa_circ_199397 19156 RMVar_ID_19156 Human_SNP_ID_69502622 A-to-I Human chr2 - 43920411 43920411 43920411 TAGGCTGCAGCTGGGCAAGGTGGCTCACACCTATAATCCCAGCACTTTGGGAGGCCAAGGCCAGT TAGGCTGCAGCTGGGCAAGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGCCAGT T C LRPPRC Ensembl:ENSG00000138095 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1468725975 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6922457,Human_RBP_ID_13892300 RMVar_hsa_circ_2968,RMVar_hsa_circ_628,RMVar_hsa_circ_23322,RMVar_hsa_circ_57044,RMVar_hsa_circ_267196,RMVar_hsa_circ_42731,RMVar_hsa_circ_33116,RMVar_hsa_circ_121609,RMVar_hsa_circ_334855,RMVar_hsa_circ_56178,RMVar_hsa_circ_308772,RMVar_hsa_circ_199381,RMVar_hsa_circ_199382,RMVar_hsa_circ_59979,RMVar_hsa_circ_305149,RMVar_hsa_circ_199383,RMVar_hsa_circ_25563,RMVar_hsa_circ_341074,RMVar_hsa_circ_365415,RMVar_hsa_circ_313240,RMVar_hsa_circ_65860,RMVar_hsa_circ_78179,RMVar_hsa_circ_42425,RMVar_hsa_circ_199391,RMVar_hsa_circ_340645,RMVar_hsa_circ_114021,RMVar_hsa_circ_199385,RMVar_hsa_circ_199387,RMVar_hsa_circ_199388,RMVar_hsa_circ_199386,RMVar_hsa_circ_268053,RMVar_hsa_circ_355943,RMVar_hsa_circ_373562,RMVar_hsa_circ_375386,RMVar_hsa_circ_199389,RMVar_hsa_circ_374357,RMVar_hsa_circ_368467,RMVar_hsa_circ_342103,RMVar_hsa_circ_21576,RMVar_hsa_circ_273864,RMVar_hsa_circ_199393,RMVar_hsa_circ_199395,RMVar_hsa_circ_199394,RMVar_hsa_circ_199392,RMVar_hsa_circ_19510,RMVar_hsa_circ_283018,RMVar_hsa_circ_341842,RMVar_hsa_circ_352126,RMVar_hsa_circ_199390,RMVar_hsa_circ_361710,RMVar_hsa_circ_344611,RMVar_hsa_circ_305321,RMVar_hsa_circ_57799,RMVar_hsa_circ_38372,RMVar_hsa_circ_90303,RMVar_hsa_circ_199398,RMVar_hsa_circ_199399,RMVar_hsa_circ_125985,RMVar_hsa_circ_360198,RMVar_hsa_circ_370464,RMVar_hsa_circ_285728,RMVar_hsa_circ_110840,RMVar_hsa_circ_199403,RMVar_hsa_circ_54086,RMVar_hsa_circ_199405,RMVar_hsa_circ_199404,RMVar_hsa_circ_199401,RMVar_hsa_circ_199402,RMVar_hsa_circ_30854,RMVar_hsa_circ_365369 19157 RMVar_ID_19157 Human_SNP_ID_69509257 A-to-I Human chr2 - 43942876 43942876 43942876 GATAATAATTAAAATAAAATAAAATGGAAGATATACGTATCTGAAAGTAGTAAAACACCGAAAAT GATAATAATTAAAATAAAATAAAATGGAAGATGTACGTATCTGAAAGTAGTAAAACACCGAAAAT T C LRPPRC Ensembl:ENSG00000138095 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041992925 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2968,RMVar_hsa_circ_628,RMVar_hsa_circ_23322,RMVar_hsa_circ_267196,RMVar_hsa_circ_42731,RMVar_hsa_circ_33116,RMVar_hsa_circ_334855,RMVar_hsa_circ_56178,RMVar_hsa_circ_199381,RMVar_hsa_circ_59979,RMVar_hsa_circ_25563,RMVar_hsa_circ_341074,RMVar_hsa_circ_365415,RMVar_hsa_circ_313240,RMVar_hsa_circ_65860,RMVar_hsa_circ_199391,RMVar_hsa_circ_340645,RMVar_hsa_circ_114021,RMVar_hsa_circ_199387,RMVar_hsa_circ_199388,RMVar_hsa_circ_373562,RMVar_hsa_circ_375386,RMVar_hsa_circ_199389,RMVar_hsa_circ_374357,RMVar_hsa_circ_368467,RMVar_hsa_circ_342103,RMVar_hsa_circ_21576,RMVar_hsa_circ_199393,RMVar_hsa_circ_199394,RMVar_hsa_circ_199392,RMVar_hsa_circ_19510,RMVar_hsa_circ_341842,RMVar_hsa_circ_352126,RMVar_hsa_circ_199390,RMVar_hsa_circ_361710,RMVar_hsa_circ_344611,RMVar_hsa_circ_57799,RMVar_hsa_circ_38372,RMVar_hsa_circ_90303,RMVar_hsa_circ_199399,RMVar_hsa_circ_125985,RMVar_hsa_circ_360198,RMVar_hsa_circ_370464,RMVar_hsa_circ_110840,RMVar_hsa_circ_199403,RMVar_hsa_circ_54086,RMVar_hsa_circ_199404,RMVar_hsa_circ_199401,RMVar_hsa_circ_199402,RMVar_hsa_circ_30854,RMVar_hsa_circ_42403,RMVar_hsa_circ_45086,RMVar_hsa_circ_87978,RMVar_hsa_circ_337694,RMVar_hsa_circ_344002,RMVar_hsa_circ_367195,RMVar_hsa_circ_342954,RMVar_hsa_circ_50582,RMVar_hsa_circ_47870,RMVar_hsa_circ_117698,RMVar_hsa_circ_199408,RMVar_hsa_circ_11662,RMVar_hsa_circ_199409,RMVar_hsa_circ_336002,RMVar_hsa_circ_295825,RMVar_hsa_circ_68820,RMVar_hsa_circ_44563,RMVar_hsa_circ_199412,RMVar_hsa_circ_344593,RMVar_hsa_circ_199411,RMVar_hsa_circ_199410,RMVar_hsa_circ_370902,RMVar_hsa_circ_373603,RMVar_hsa_circ_349486,RMVar_hsa_circ_330960,RMVar_hsa_circ_336582,RMVar_hsa_circ_300448,RMVar_hsa_circ_199414,RMVar_hsa_circ_199415,RMVar_hsa_circ_199416,RMVar_hsa_circ_199413,RMVar_hsa_circ_92362,RMVar_hsa_circ_319886,RMVar_hsa_circ_370054,RMVar_hsa_circ_111304,RMVar_hsa_circ_90783,RMVar_hsa_circ_199418,RMVar_hsa_circ_199420,RMVar_hsa_circ_199421,RMVar_hsa_circ_199419,RMVar_hsa_circ_199417 19158 RMVar_ID_19158 Human_SNP_ID_69521359 A-to-I Human chr2 - 43980437 43980437 43980437 GCAGTTCTCCTGCCTCAGCCTCCCGAGTAGCTAGAATTACAGGCATGCGCCATCTCGCCCAGCTA GCAGTTCTCCTGCCTCAGCCTCCCGAGTAGCTTGAATTACAGGCATGCGCCATCTCGCCCAGCTA T A LRPPRC Ensembl:ENSG00000138095 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs544099698 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2968,RMVar_hsa_circ_56178,RMVar_hsa_circ_59979,RMVar_hsa_circ_313240,RMVar_hsa_circ_199388,RMVar_hsa_circ_368467,RMVar_hsa_circ_341842,RMVar_hsa_circ_344002,RMVar_hsa_circ_199412,RMVar_hsa_circ_300448,RMVar_hsa_circ_370054,RMVar_hsa_circ_199421,RMVar_hsa_circ_331317,RMVar_hsa_circ_199422,RMVar_hsa_circ_199429,RMVar_hsa_circ_373358,RMVar_hsa_circ_351788,RMVar_hsa_circ_110264,RMVar_hsa_circ_199434,RMVar_hsa_circ_369420,RMVar_hsa_circ_89737,RMVar_hsa_circ_199438,RMVar_hsa_circ_199441,RMVar_hsa_circ_284637,RMVar_hsa_circ_126864,RMVar_hsa_circ_305000,RMVar_hsa_circ_297213,RMVar_hsa_circ_199446,RMVar_hsa_circ_278324,RMVar_hsa_circ_199453,RMVar_hsa_circ_53518,RMVar_hsa_circ_30541,RMVar_hsa_circ_199457,RMVar_hsa_circ_349425,RMVar_hsa_circ_76830,RMVar_hsa_circ_199460,RMVar_hsa_circ_122331,RMVar_hsa_circ_341857,RMVar_hsa_circ_199465,RMVar_hsa_circ_199464,RMVar_hsa_circ_199466,RMVar_hsa_circ_335220,RMVar_hsa_circ_305296 19159 RMVar_ID_19159 Human_SNP_ID_69521767 A-to-I Human chr2 - 43981515 43981515 43981515 GTAGCTGGGACTACCGATGCATGCCACTGCCCAGCTAATTTTTGTATTTTTAGTAGGGACGGGGT GTAGCTGGGACTACCGATGCATGCCACTGCCCGGCTAATTTTTGTATTTTTAGTAGGGACGGGGT T C LRPPRC Ensembl:ENSG00000138095 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1281211750 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2968,RMVar_hsa_circ_56178,RMVar_hsa_circ_59979,RMVar_hsa_circ_313240,RMVar_hsa_circ_199388,RMVar_hsa_circ_368467,RMVar_hsa_circ_341842,RMVar_hsa_circ_344002,RMVar_hsa_circ_199412,RMVar_hsa_circ_300448,RMVar_hsa_circ_370054,RMVar_hsa_circ_199421,RMVar_hsa_circ_331317,RMVar_hsa_circ_199422,RMVar_hsa_circ_199429,RMVar_hsa_circ_373358,RMVar_hsa_circ_351788,RMVar_hsa_circ_110264,RMVar_hsa_circ_199434,RMVar_hsa_circ_369420,RMVar_hsa_circ_89737,RMVar_hsa_circ_199438,RMVar_hsa_circ_199441,RMVar_hsa_circ_284637,RMVar_hsa_circ_126864,RMVar_hsa_circ_305000,RMVar_hsa_circ_297213,RMVar_hsa_circ_199446,RMVar_hsa_circ_278324,RMVar_hsa_circ_199453,RMVar_hsa_circ_53518,RMVar_hsa_circ_30541,RMVar_hsa_circ_199457,RMVar_hsa_circ_349425,RMVar_hsa_circ_76830,RMVar_hsa_circ_199460,RMVar_hsa_circ_122331,RMVar_hsa_circ_341857,RMVar_hsa_circ_199465,RMVar_hsa_circ_199464,RMVar_hsa_circ_199466,RMVar_hsa_circ_335220,RMVar_hsa_circ_305296 19160 RMVar_ID_19160 Human_SNP_ID_69521784 A-to-I Human chr2 - 43981557 43981557 43981557 TGCCTCCCGGGTTCAAGCAACTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACCGATGCATG TGCCTCCCGGGTTCAAGCAACTCTCCTGCCTCGGCCTCCCAAGTAGCTGGGACTACCGATGCATG T C LRPPRC Ensembl:ENSG00000138095 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1205162469 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2968,RMVar_hsa_circ_56178,RMVar_hsa_circ_59979,RMVar_hsa_circ_313240,RMVar_hsa_circ_199388,RMVar_hsa_circ_368467,RMVar_hsa_circ_341842,RMVar_hsa_circ_344002,RMVar_hsa_circ_199412,RMVar_hsa_circ_300448,RMVar_hsa_circ_370054,RMVar_hsa_circ_199421,RMVar_hsa_circ_331317,RMVar_hsa_circ_199422,RMVar_hsa_circ_199429,RMVar_hsa_circ_373358,RMVar_hsa_circ_351788,RMVar_hsa_circ_110264,RMVar_hsa_circ_199434,RMVar_hsa_circ_369420,RMVar_hsa_circ_89737,RMVar_hsa_circ_199438,RMVar_hsa_circ_199441,RMVar_hsa_circ_284637,RMVar_hsa_circ_126864,RMVar_hsa_circ_305000,RMVar_hsa_circ_297213,RMVar_hsa_circ_199446,RMVar_hsa_circ_278324,RMVar_hsa_circ_199453,RMVar_hsa_circ_53518,RMVar_hsa_circ_30541,RMVar_hsa_circ_199457,RMVar_hsa_circ_349425,RMVar_hsa_circ_76830,RMVar_hsa_circ_199460,RMVar_hsa_circ_122331,RMVar_hsa_circ_341857,RMVar_hsa_circ_199465,RMVar_hsa_circ_199464,RMVar_hsa_circ_199466,RMVar_hsa_circ_335220,RMVar_hsa_circ_305296 19161 RMVar_ID_19161 Human_SNP_ID_69524042 A-to-I Human chr2 - 43988118 43988118 43988118 CTCCTGCCTCAGCCTTCTGAGTTGCTGGGATTACAGGCACCTGCCACCATGCCCGGCTTATTTTT CTCCTGCCTCAGCCTTCTGAGTTGCTGGGATTCCAGGCACCTGCCACCATGCCCGGCTTATTTTT T G LRPPRC Ensembl:ENSG00000138095 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1480980173 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126864,RMVar_hsa_circ_199446,RMVar_hsa_circ_122331,RMVar_hsa_circ_199465 19162 RMVar_ID_19162 Human_SNP_ID_69526480 A-to-I Human chr2 - 43995075 43995075 43995075 CACCATGCCAGGCTAACTTTTGTACTTTTAGTAGAGACTGGGTTTCACCATGTTGGCCACGCTAG CACCATGCCAGGCTAACTTTTGTACTTTTAGTGGAGACTGGGTTTCACCATGTTGGCCACGCTAG T C LRPPRC Ensembl:ENSG00000138095 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1483022616 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126864,RMVar_hsa_circ_199446,RMVar_hsa_circ_122331,RMVar_hsa_circ_199465 19163 RMVar_ID_19163 Human_SNP_ID_69526482 A-to-I Human chr2 - 43995078 43995078 43995078 CGCCACCATGCCAGGCTAACTTTTGTACTTTTAGTAGAGACTGGGTTTCACCATGTTGGCCACGC CGCCACCATGCCAGGCTAACTTTTGTACTTTTTGTAGAGACTGGGTTTCACCATGTTGGCCACGC T A LRPPRC Ensembl:ENSG00000138095 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042404546 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126864,RMVar_hsa_circ_199446,RMVar_hsa_circ_122331,RMVar_hsa_circ_199465 19164 RMVar_ID_19164 Human_SNP_ID_69526509 A-to-I Human chr2 - 43995158 43995158 43995158 CAGCTCACTGCAACTTCCGCTTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCT CAGCTCACTGCAACTTCCGCTTCCCGGGTTCAGGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCT T C LRPPRC Ensembl:ENSG00000138095 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027498374 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126864,RMVar_hsa_circ_199446,RMVar_hsa_circ_122331,RMVar_hsa_circ_199465 19165 RMVar_ID_19165 Human_SNP_ID_69602436 A-to-I Human chr2 + 44223046 44223046 44223046 TAGGGATAGGGTCTCGCTTCATTGCCAGGGCTAGTCTTGAACTCCTGGGCTCAAGTTATCTTCCT TAGGGATAGGGTCTCGCTTCATTGCCAGGGCTGGTCTTGAACTCCTGGGCTCAAGTTATCTTCCT A G PPM1B,AC013717.1 Ensembl:ENSG00000138032,Ensembl:ENSG00000285542 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1209817028 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92064,RMVar_hsa_circ_199468,RMVar_hsa_circ_199475 19166 RMVar_ID_19166 Human_SNP_ID_69602598 A-to-I Human chr2 + 44223554 44223554 44223554 AATGCAGGCCGGGCGCGGTGGCTCATGCCTGTAATGCCAGCACTTTGGGAGGGCGAGGCAGGAGG AATGCAGGCCGGGCGCGGTGGCTCATGCCTGTCATGCCAGCACTTTGGGAGGGCGAGGCAGGAGG A C PPM1B,AC013717.1 Ensembl:ENSG00000138032,Ensembl:ENSG00000285542 Protein coding,Protein coding intron,intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1427284058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13895698 RMVar_hsa_circ_92064,RMVar_hsa_circ_199468 19167 RMVar_ID_19167 Human_SNP_ID_69603948 A-to-I Human chr2 + 44227255 44227255 44227255 CCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCAGCCCTGGATGAGAAACTTTATT CCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCAGCCCTGGATGAGAAACTTTATT A G PPM1B,AC013717.1 Ensembl:ENSG00000138032,Ensembl:ENSG00000285542 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1016025985 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92064,RMVar_hsa_circ_199468 19168 RMVar_ID_19168 Human_SNP_ID_69608625 A-to-I Human chr2 + 44241470 44241470 44241470 AAATGTCTTCAAGGCCAGGCTCGGTGGCTCACACCTGTAATCCCGGCACTATGGGAGGGCCACCT AAATGTCTTCAAGGCCAGGCTCGGTGGCTCACGCCTGTAATCCCGGCACTATGGGAGGGCCACCT A G PPM1B,AC013717.1 Ensembl:ENSG00000138032,Ensembl:ENSG00000285542 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1478358940 Functional Loss SNV dbSNP153 33..33 33 - - - 19169 RMVar_ID_19169 Human_SNP_ID_69632630 A-to-I Human chr2 - 44314994 44314994 44314994 CCAGGAGATGGAGGTTGCGGTGAGCCAAGACCACACCATTGCACTCTAGCCCGGGCAACAAAAGC CCAGGAGATGGAGGTTGCGGTGAGCCAAGACCGCACCATTGCACTCTAGCCCGGGCAACAAAAGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs995066542 Functional Loss SNV dbSNP153 33..33 33 - - - 19170 RMVar_ID_19170 Human_SNP_ID_69633862 A-to-I Human chr2 - 44318153 44318153 44318153 CCAGGAAGCAGAGGCTGCAGTGTGCCGAGATCACGCCACTGCACTCGAGCATGGGTGACGGAGCA CCAGGAAGCAGAGGCTGCAGTGTGCCGAGATCCCGCCACTGCACTCGAGCATGGGTGACGGAGCA T G PREPL Ensembl:ENSG00000138078 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1368912991 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_551429,Human_RBP_ID_25544910 19171 RMVar_ID_19171 Human_SNP_ID_69643313 A-to-I Human chr2 - 44347279 44347279 44347279 CATGCTGGAGTGCAATGGCATGATCATGCTTCACTGCAGCCTCAACCTCCTGGGCTCAGGTGATC CATGCTGGAGTGCAATGGCATGATCATGCTTCGCTGCAGCCTCAACCTCCTGGGCTCAGGTGATC T C PREPL Ensembl:ENSG00000138078 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1318472722 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_241554,Human_Splice_Rec_241555 19172 RMVar_ID_19172 Human_SNP_ID_69645817 A-to-I Human chr2 - 44355492 44355492 44355492 CAGTCTGTAGTGCAGTGGCACAGTCTCTGCTCACTGCAACCTCCACCTCCCAGGCTCAAGTGATT CAGTCTGTAGTGCAGTGGCACAGTCTCTGCTCGCTGCAACCTCCACCTCCCAGGCTCAAGTGATT T C PREPL Ensembl:ENSG00000138078 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,cerebellum - 29129909,30559470 RNA-Seq:(High) rs971731122 Functional Loss SNV dbSNP153 33..33 33 - - - 19173 RMVar_ID_19173 Human_SNP_ID_69646165 A-to-I Human chr2 - 44356437 44356437 44356437 AGATTCAGGCAATTCTCCTGCCTCAGCTGCCAAGTAGCTGGGATTACAGGCGTCCACCACCATGC AGATTCAGGCAATTCTCCTGCCTCAGCTGCCAGGTAGCTGGGATTACAGGCGTCCACCACCATGC T C PREPL Ensembl:ENSG00000138078 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1484058047 Functional Loss SNV dbSNP153 33..33 33 - - - 19174 RMVar_ID_19174 Human_SNP_ID_69646166 A-to-I Human chr2 - 44356437 44356437 44356437 AGATTCAGGCAATTCTCCTGCCTCAGCTGCCAAGTAGCTGGGATTACAGGCGTCCACCACCATGC AGATTCAGGCAATTCTCCTGCCTCAGCTGCCACGTAGCTGGGATTACAGGCGTCCACCACCATGC T G PREPL Ensembl:ENSG00000138078 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1484058047 Functional Loss SNV dbSNP153 33..33 33 - - - 19175 RMVar_ID_19175 Human_SNP_ID_69659899 A-to-I Human chr2 + 44402069 44402069 44402069 ATAGAATTGGCCGGGCGCGGTGGCTCACGCCTATAGTCCCAGGACTTTGGGAGGCCAAGGCGGGT ATAGAATTGGCCGGGCGCGGTGGCTCACGCCTGTAGTCCCAGGACTTTGGGAGGCCAAGGCGGGT A G CAMKMT Ensembl:ENSG00000143919 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs542672062 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7903 19176 RMVar_ID_19176 Human_SNP_ID_69659930 A-to-I Human chr2 + 44402166 44402148 44402166 CTGGCCAACATGGTGAAACCCCGTCTCTACTAAAGATACAAAAAAATTAGCCAGGCCTGGTGGCA CTGGCCAACATGGTG__________________AGATACAAAAAAATTAGCCAGGCCTGGTGGCA GAAACCCCGTCTCTACTAA G CAMKMT Ensembl:ENSG00000143919 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1275775456 Functional Loss DEL dbSNP153 16..33 33 - - - RMVar_hsa_circ_7903 19177 RMVar_ID_19177 Human_SNP_ID_69661326 A-to-I Human chr2 + 44406822 44406822 44406822 GGTTTCTCCATGTTGCCCAGCCAGGCTGGTCTAGAACTCCTGGGCTCAAGCAATCCGCCCACCAC GGTTTCTCCATGTTGCCCAGCCAGGCTGGTCTGGAACTCCTGGGCTCAAGCAATCCGCCCACCAC A G CAMKMT Ensembl:ENSG00000143919 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569147981 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13897046 RMVar_hsa_circ_7903 19178 RMVar_ID_19178 Human_SNP_ID_69663071 A-to-I Human chr2 + 44412415 44412415 44412415 TGAAGTACAATGGCACAATCTTGGCTCACTGCAACCTCTGCCTCCCAGGTTCAAGCAATTCTCCT TGAAGTACAATGGCACAATCTTGGCTCACTGCTACCTCTGCCTCCCAGGTTCAAGCAATTCTCCT A T CAMKMT Ensembl:ENSG00000143919 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1015198637 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7903 19179 RMVar_ID_19179 Human_SNP_ID_69664757 A-to-I Human chr2 + 44418069 44418067 44418069 TAAAAAGTAGTCGGGCATGGTGGCACGTGCCTATAATCCCAAATACTCTGGAGGCTGAGGCGGGA TAAAAAGTAGTCGGGCATGGTGGCACGTGCC__TAATCCCAAATACTCTGGAGGCTGAGGCGGGA CTA C CAMKMT Ensembl:ENSG00000143919 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs771713069 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_25545332 RMVar_hsa_circ_7903 19180 RMVar_ID_19180 Human_SNP_ID_69664758 A-to-I Human chr2 + 44418069 44418069 44418069 TAAAAAGTAGTCGGGCATGGTGGCACGTGCCTATAATCCCAAATACTCTGGAGGCTGAGGCGGGA TAAAAAGTAGTCGGGCATGGTGGCACGTGCCTGTAATCCCAAATACTCTGGAGGCTGAGGCGGGA A G CAMKMT Ensembl:ENSG00000143919 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1258993052 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25545332 RMVar_hsa_circ_7903 19181 RMVar_ID_19181 Human_SNP_ID_69684806 A-to-I Human chr2 + 44491030 44491030 44491030 AAAAAATTAGCTGGGCATGGTGGCATGCCTGTAGTCTCAGCTACTTGGGAGGCGGAGGTGGGAGG AAAAAATTAGCTGGGCATGGTGGCATGCCTGTCGTCTCAGCTACTTGGGAGGCGGAGGTGGGAGG A C CAMKMT Ensembl:ENSG00000143919 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1222257656 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7903 19182 RMVar_ID_19182 Human_SNP_ID_69697700 A-to-I Human chr2 + 44537737 44537737 44537737 GGGCATGTGCCAACACGGTCAGCTAATTTTTTATATTTTGTAGAAACAGAGTCTTGCAATGTTGT GGGCATGTGCCAACACGGTCAGCTAATTTTTTGTATTTTGTAGAAACAGAGTCTTGCAATGTTGT A G CAMKMT Ensembl:ENSG00000143919 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1002180291 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7903,RMVar_hsa_circ_199490,RMVar_hsa_circ_199489 19183 RMVar_ID_19183 Human_SNP_ID_69706102 A-to-I Human chr2 + 44568267 44568267 44568267 GAGCTTCCTCCAAATGGGACCCTACTTTCATCAGTGCATTTGCTTGGAAACTGTTACTCAAAAGT GAGCTTCCTCCAAATGGGACCCTACTTTCATCTGTGCATTTGCTTGGAAACTGTTACTCAAAAGT A T CAMKMT Ensembl:ENSG00000143919 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1014752451 Functional Loss SNV dbSNP153 33..33 33 - - - 19184 RMVar_ID_19184 Human_SNP_ID_69713586 A-to-I Human chr2 + 44593903 44593903 44593903 CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCATGTACCACCACGCCTGGCTAATTTGG CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTGCAGGCATGTACCACCACGCCTGGCTAATTTGG A G CAMKMT Ensembl:ENSG00000143919 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1239801302 Functional Loss SNV dbSNP153 33..33 33 - - - 19185 RMVar_ID_19185 Human_SNP_ID_69721786 A-to-I Human chr2 + 44624076 44624076 44624076 TCCACCCAACTGTTGATAAAACAAAAATTGGCAAGTGGGACCTAAGTAAACTAAAGAGCTAAGTA TCCACCCAACTGTTGATAAAACAAAAATTGGCCAGTGGGACCTAAGTAAACTAAAGAGCTAAGTA A C CAMKMT Ensembl:ENSG00000143919 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1305372514 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13900356 19186 RMVar_ID_19186 Human_SNP_ID_687654292 A-to-I Human chr21 - 8987106 8987106 8987106 ACCCCTCGAGCGCGGCCGACCGCAGCCGGGACACACGCGCGGGGCCTCACCGCCGCCGGCGGCAC ACCCCTCGAGCGCGGCCGACCGCAGCCGGGACGCACGCGCGGGGCCTCACCGCCGCCGGCGGCAC T C lnc-KCNE1B-10,lnc-KCNE1B-3,lnc-KCNE1B-3:2 RNACentral:URS00004687BF,RNACentral:URS0000D58B87,RNACentral:URS0000D592AB lincRNA,lincRNA,lincRNA intron,intron,intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs560916630 Functional Loss SNV dbSNP153 33..33 33 - - - 19187 RMVar_ID_19187 Human_SNP_ID_687701412 A-to-I Human chr21 - 9113898 9113898 9113898 CTACTTATTTTCTATTTGTTTGTTTTTTTTTTAAGACAGGGTCTTGCTCTGTCACCCAGACTGTA CTACTTATTTTCTATTTGTTTGTTTTTTTTTTTAGACAGGGTCTTGCTCTGTCACCCAGACTGTA T A TEKT4P2 Ensembl:ENSG00000188681 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1234472327 Functional Loss SNV dbSNP153 33..33 33 - - - 19188 RMVar_ID_19188 Human_SNP_ID_688044281 A-to-I Human chr21 - 10332826 10332824 10332826 TTTGAATAGTTGGATTTTTTTTTTCAAGACAGAGTCTCACTCTGTCACCCAGGCTGGAGTGCAGT TTTGAATAGTTGGATTTTTTTTTTCAAGACAG__TCTCACTCTGTCACCCAGGCTGGAGTGCAGT ACT A AP003900.1 Ensembl:ENSG00000277693 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1216190987 Functional Loss DEL dbSNP153 33..34 33 - - - 19189 RMVar_ID_19189 Human_SNP_ID_688567663 A-to-I Human chr21 + 14048989 14048989 14048989 ATGCACTATTATAAGTGCAATTACCTTATAATAGCCTATTCCCAATTCCTTCCCTCCATCCTTTG ATGCACTATTATAAGTGCAATTACCTTATAATGGCCTATTCCCAATTCCTTCCCTCCATCCTTTG A G AP001347.1 Ensembl:ENSG00000224905 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1305747527 Functional Loss SNV dbSNP153 33..33 33 - - - 19190 RMVar_ID_19190 Human_SNP_ID_688578860 A-to-I Human chr21 + 14081358 14081358 14081358 AAAGAAAGTACACATAGAAATTACACATAGCCAAGTGCAGTGGCTCACGCCTGTAATCTCAGCAC AAAGAAAGTACACATAGAAATTACACATAGCCGAGTGCAGTGGCTCACGCCTGTAATCTCAGCAC A G AP001347.1 Ensembl:ENSG00000224905 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs922319218 Functional Loss SNV dbSNP153 33..33 33 - - - 19191 RMVar_ID_19191 Human_SNP_ID_688580654 A-to-I Human chr21 + 14087342 14087342 14087342 TTTAGTAGAGATGGGGTTTCGCTACACTGCCCAGGCTGATCTCGACTCCTGATCTCAAGTGATCT TTTAGTAGAGATGGGGTTTCGCTACACTGCCCCGGCTGATCTCGACTCCTGATCTCAAGTGATCT A C AP001347.1 Ensembl:ENSG00000224905 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs997329704 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14186467 RMVar_hsa_circ_211444 19192 RMVar_ID_19192 Human_SNP_ID_688582579 A-to-I Human chr21 + 14093932 14093932 14093932 ATAATCAGCCAAGTGTGGTGGCGCGTGCCTGTAGTCCCAGCTACTCAGGAGGTTGAGACATGAGA ATAATCAGCCAAGTGTGGTGGCGCGTGCCTGTCGTCCCAGCTACTCAGGAGGTTGAGACATGAGA A C AP001347.1 Ensembl:ENSG00000224905 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1299909064 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_211444 19193 RMVar_ID_19193 Human_SNP_ID_688582844 A-to-I Human chr21 + 14094638 14094638 14094638 TGTGAGGCTGAGGCAGAGGATTGCTTGAACCCAGGAGTGCAAGGCTGCATTGAGCTATAATTGTG TGTGAGGCTGAGGCAGAGGATTGCTTGAACCCGGGAGTGCAAGGCTGCATTGAGCTATAATTGTG A G AP001347.1 Ensembl:ENSG00000224905 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1485645339 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8261473,Human_RBP_ID_14186632 RMVar_hsa_circ_211444 19194 RMVar_ID_19194 Human_SNP_ID_688585578 A-to-I Human chr21 + 14105684 14105684 14105684 TCAAGTGGTCAGCTCACCTCGGCCGGCCTCCCAAAGTGCTGGGATGACAGGCATGAGCCACTGCG TCAAGTGGTCAGCTCACCTCGGCCGGCCTCCCGAAGTGCTGGGATGACAGGCATGAGCCACTGCG A G AP001347.1 Ensembl:ENSG00000224905 lincRNA intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1193249500 Functional Loss SNV dbSNP153 33..33 33 - - - 19195 RMVar_ID_19195 Human_SNP_ID_688756869 A-to-I Human chr21 + 14757741 14757741 14757741 TTCTTCATGATGAGTTCATGGCTCACAAACTTAGATTAATTCCCCTCATTAGTGAGGACATTGTG TTCTTCATGATGAGTTCATGGCTCACAAACTTGGATTAATTCCCCTCATTAGTGAGGACATTGTG A G POLR2CP1 Ensembl:ENSG00000228600 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1378184186 Functional Loss SNV dbSNP153 33..33 33 - - - 19196 RMVar_ID_19196 Human_SNP_ID_688933873 A-to-I Human chr21 - 15434654 15434654 15434654 GGCACTTTTGCATGCTGAGCACTTTGTATTAAAGGAAGTTGGAAGGACTTAGAAGCTGCCCCAGA GGCACTTTTGCATGCTGAGCACTTTGTATTAATGGAAGTTGGAAGGACTTAGAAGCTGCCCCAGA T A AJ009632.2 Ensembl:ENSG00000229425 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1485680757 Functional Loss SNV dbSNP153 33..33 33 - - - 19197 RMVar_ID_19197 Human_SNP_ID_688933874 A-to-I Human chr21 - 15434654 15434654 15434654 GGCACTTTTGCATGCTGAGCACTTTGTATTAAAGGAAGTTGGAAGGACTTAGAAGCTGCCCCAGA GGCACTTTTGCATGCTGAGCACTTTGTATTAAGGGAAGTTGGAAGGACTTAGAAGCTGCCCCAGA T C AJ009632.2 Ensembl:ENSG00000229425 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1485680757 Functional Loss SNV dbSNP153 33..33 33 - - - 19198 RMVar_ID_19198 Human_SNP_ID_689034165 A-to-I Human chr21 + 15816072 15816072 15816072 GCTGTGTCCTGATGTAAATCTCAACTTGAATTATATCTCCCAGAGTTCCCACATGTTGTGGGAGG GCTGTGTCCTGATGTAAATCTCAACTTGAATTGTATCTCCCAGAGTTCCCACATGTTGTGGGAGG A G USP25 Ensembl:ENSG00000155313 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1294167208 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_211475,RMVar_hsa_circ_316558,RMVar_hsa_circ_358741,RMVar_hsa_circ_119210,RMVar_hsa_circ_211476,RMVar_hsa_circ_118924,RMVar_hsa_circ_369415,RMVar_hsa_circ_95553,RMVar_hsa_circ_59647,RMVar_hsa_circ_31974,RMVar_hsa_circ_211491,RMVar_hsa_circ_211487,RMVar_hsa_circ_211489,RMVar_hsa_circ_211490,RMVar_hsa_circ_211488,RMVar_hsa_circ_317960,RMVar_hsa_circ_314238,RMVar_hsa_circ_273736,RMVar_hsa_circ_281219,RMVar_hsa_circ_68388,RMVar_hsa_circ_211493,RMVar_hsa_circ_211494,RMVar_hsa_circ_211492,RMVar_hsa_circ_50476,RMVar_hsa_circ_352488,RMVar_hsa_circ_359472,RMVar_hsa_circ_362132,RMVar_hsa_circ_359921,RMVar_hsa_circ_303702,RMVar_hsa_circ_38070,RMVar_hsa_circ_54332,RMVar_hsa_circ_211499,RMVar_hsa_circ_211500,RMVar_hsa_circ_333790,RMVar_hsa_circ_341887,RMVar_hsa_circ_304607,RMVar_hsa_circ_283135,RMVar_hsa_circ_289302,RMVar_hsa_circ_59988,RMVar_hsa_circ_211503,RMVar_hsa_circ_211505,RMVar_hsa_circ_15280,RMVar_hsa_circ_211504,RMVar_hsa_circ_211501,RMVar_hsa_circ_211502,RMVar_hsa_circ_285086,RMVar_hsa_circ_351914,RMVar_hsa_circ_353132,RMVar_hsa_circ_328700,RMVar_hsa_circ_60891,RMVar_hsa_circ_36622,RMVar_hsa_circ_36763,RMVar_hsa_circ_211509,RMVar_hsa_circ_211510,RMVar_hsa_circ_211508,RMVar_hsa_circ_293577,RMVar_hsa_circ_320633,RMVar_hsa_circ_350355,RMVar_hsa_circ_295863,RMVar_hsa_circ_65540,RMVar_hsa_circ_211513,RMVar_hsa_circ_211514,RMVar_hsa_circ_211512,RMVar_hsa_circ_281898,RMVar_hsa_circ_359936,RMVar_hsa_circ_364590,RMVar_hsa_circ_370548,RMVar_hsa_circ_310457,RMVar_hsa_circ_120291,RMVar_hsa_circ_211516,RMVar_hsa_circ_211517,RMVar_hsa_circ_211518,RMVar_hsa_circ_211515 19199 RMVar_ID_19199 Human_SNP_ID_689039695 A-to-I Human chr21 + 15837900 15837900 15837900 GAGTAAGACCTGGTAGAATAAACAGTATCGTCAGTGTTCTCAGATTCCTTGAAAGCAGGAACTAG GAGTAAGACCTGGTAGAATAAACAGTATCGTCGGTGTTCTCAGATTCCTTGAAAGCAGGAACTAG A G USP25 Ensembl:ENSG00000155313 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs536931737 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9120336,Human_RBP_ID_14194237 RMVar_hsa_circ_211475,RMVar_hsa_circ_316558,RMVar_hsa_circ_119210,RMVar_hsa_circ_211476,RMVar_hsa_circ_95553,RMVar_hsa_circ_211491,RMVar_hsa_circ_211490,RMVar_hsa_circ_273736,RMVar_hsa_circ_68388,RMVar_hsa_circ_50476,RMVar_hsa_circ_362132,RMVar_hsa_circ_303702,RMVar_hsa_circ_38070,RMVar_hsa_circ_211500,RMVar_hsa_circ_283135,RMVar_hsa_circ_289302,RMVar_hsa_circ_59988,RMVar_hsa_circ_211501,RMVar_hsa_circ_211502,RMVar_hsa_circ_285086,RMVar_hsa_circ_36763,RMVar_hsa_circ_211510,RMVar_hsa_circ_350355,RMVar_hsa_circ_281898,RMVar_hsa_circ_370548,RMVar_hsa_circ_211516,RMVar_hsa_circ_211515,RMVar_hsa_circ_343381,RMVar_hsa_circ_211522,RMVar_hsa_circ_294176,RMVar_hsa_circ_32799,RMVar_hsa_circ_211524,RMVar_hsa_circ_266368,RMVar_hsa_circ_71709,RMVar_hsa_circ_347032,RMVar_hsa_circ_45666,RMVar_hsa_circ_74735,RMVar_hsa_circ_294049,RMVar_hsa_circ_68697,RMVar_hsa_circ_92244,RMVar_hsa_circ_70053,RMVar_hsa_circ_211525,RMVar_hsa_circ_211526,RMVar_hsa_circ_211527 19200 RMVar_ID_19200 Human_SNP_ID_689050477 A-to-I Human chr21 + 15878686 15878686 15878686 CGCATGGCGCTCAGACATTTTAACCGGAACTGATGTATAATCACAAATCTAATTGATTTTATTAT CGCATGGCGCTCAGACATTTTAACCGGAACTGGTGTATAATCACAAATCTAATTGATTTTATTAT A G USP25 Ensembl:ENSG00000155313 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1341090518 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_569617,Human_RBP_ID_1601705,Human_RBP_ID_1933803,Human_RBP_ID_8539475,Human_RBP_ID_14195402,Human_RBP_ID_18778043,Human_RBP_ID_26672597,Human_RBP_ID_27300467,Human_RBP_ID_27489214 RMVar_hsa_circ_211528 19201 RMVar_ID_19201 Human_SNP_ID_689181546 A-to-I Human chr21 + 16391663 16391659 16391664 AAGAGAATTCTCAATGTCAAGATTTGAACAAGAAGAGAATGGAATACACAATATGGTAAGTGACT AAGAGAATTCTCAATGTCAAGATTTGAAC_____GAGAATGGAATACACAATATGGTAAGTGACT CAAGAA C MIR99AHG Ensembl:ENSG00000215386 lincRNA exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1356006899 Functional Loss DEL dbSNP153 30..34 33 - - - Human_RBP_ID_1933876,Human_RBP_ID_5598786,Human_RBP_ID_8261874 Human_Splice_Rec_2108822,Human_Splice_Rec_2108823,Human_Splice_Rec_2108834,Human_Splice_Rec_2108835,Human_Splice_Rec_2108854,Human_Splice_Rec_2108855,Human_Splice_Rec_2108872,Human_Splice_Rec_2108873,Human_Splice_Rec_2108888,Human_Splice_Rec_2108889,Human_Splice_Rec_2108898,Human_Splice_Rec_2108899,Human_Splice_Rec_2108910,Human_Splice_Rec_2108911,Human_Splice_Rec_2108924,Human_Splice_Rec_2108925,Human_Splice_Rec_2108936,Human_Splice_Rec_2108937,Human_Splice_Rec_2108960,Human_Splice_Rec_2108961,Human_Splice_Rec_2108992,Human_Splice_Rec_2108993,Human_Splice_Rec_2109020,Human_Splice_Rec_2109021,Human_Splice_Rec_2109030,Human_Splice_Rec_2109031,Human_Splice_Rec_2109044,Human_Splice_Rec_2109045,Human_Splice_Rec_2109072,Human_Splice_Rec_2109073,Human_Splice_Rec_2109098,Human_Splice_Rec_2109099,Human_Splice_Rec_2109110,Human_Splice_Rec_2109111,Human_Splice_Rec_2109134,Human_Splice_Rec_2109135,Human_Splice_Rec_2109162,Human_Splice_Rec_2109163,Human_Splice_Rec_2109174,Human_Splice_Rec_2109175,Human_Splice_Rec_2109188,Human_Splice_Rec_2109189,Human_Splice_Rec_2109222,Human_Splice_Rec_2109223,Human_Splice_Rec_2109234,Human_Splice_Rec_2109235,Human_Splice_Rec_2109248,Human_Splice_Rec_2109249,Human_Splice_Rec_2109266,Human_Splice_Rec_2109267,Human_Splice_Rec_2109276,Human_Splice_Rec_2109277,Human_Splice_Rec_2109286,Human_Splice_Rec_2109287,Human_Splice_Rec_2109296,Human_Splice_Rec_2109297,Human_Splice_Rec_2109306,Human_Splice_Rec_2109307,Human_Splice_Rec_2109320,Human_Splice_Rec_2109321,Human_Splice_Rec_2109330,Human_Splice_Rec_2109331,Human_Splice_Rec_2109338,Human_Splice_Rec_2109339,Human_Splice_Rec_2109344,Human_Splice_Rec_2109345,Human_Splice_Rec_2109356,Human_Splice_Rec_2109357,Human_Splice_Rec_2109364,Human_Splice_Rec_2109365,Human_Splice_Rec_2109376,Human_Splice_Rec_2109377,Human_Splice_Rec_2109392,Human_Splice_Rec_2109393,Human_Splice_Rec_2109408,Human_Splice_Rec_2109409,Human_Splice_Rec_2109414,Human_Splice_Rec_2109415,Human_Splice_Rec_2109422,Human_Splice_Rec_2109423,Human_Splice_Rec_2109430,Human_Splice_Rec_2109431,Human_Splice_Rec_2109436,Human_Splice_Rec_2109437,Human_Splice_Rec_2109446,Human_Splice_Rec_2109447,Human_Splice_Rec_2109462,Human_Splice_Rec_2109463,Human_Splice_Rec_2109482,Human_Splice_Rec_2109483,Human_Splice_Rec_2109488,Human_Splice_Rec_2109489,Human_Splice_Rec_2109496,Human_Splice_Rec_2109497,Human_Splice_Rec_2109504,Human_Splice_Rec_2109505,Human_Splice_Rec_2109516,Human_Splice_Rec_2109517,Human_Splice_Rec_2109528,Human_Splice_Rec_2109529,Human_Splice_Rec_2109538,Human_Splice_Rec_2109539,Human_Splice_Rec_2109548,Human_Splice_Rec_2109549,Human_Splice_Rec_2109558,Human_Splice_Rec_2109559,Human_Splice_Rec_2109574,Human_Splice_Rec_2109575,Human_Splice_Rec_2109586,Human_Splice_Rec_2109587,Human_Splice_Rec_2109600,Human_Splice_Rec_2109601,Human_Splice_Rec_2109614,Human_Splice_Rec_2109615,Human_Splice_Rec_2109630,Human_Splice_Rec_2109631,Human_Splice_Rec_2109642,Human_Splice_Rec_2109643,Human_Splice_Rec_2109652,Human_Splice_Rec_2109653,Human_Splice_Rec_2109662,Human_Splice_Rec_2109663,Human_Splice_Rec_2109672,Human_Splice_Rec_2109673,Human_Splice_Rec_2109680,Human_Splice_Rec_2109681,Human_Splice_Rec_2109688,Human_Splice_Rec_2109689,Human_Splice_Rec_2109698,Human_Splice_Rec_2109699 RMVar_hsa_circ_21981,RMVar_hsa_circ_290327,RMVar_hsa_circ_349730,RMVar_hsa_circ_53998,RMVar_hsa_circ_211539 19202 RMVar_ID_19202 Human_SNP_ID_689184246 A-to-I Human chr21 + 16401219 16401219 16401219 TTCAAGAACAGGTGCAGGCTGGGTGTGGCCACACCTGTAATCCCAGCTACTTGGGAGGCTGAGGC TTCAAGAACAGGTGCAGGCTGGGTGTGGCCACGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGC A G MIR99AHG Ensembl:ENSG00000215386 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs918209100 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21981,RMVar_hsa_circ_349730,RMVar_hsa_circ_53998 19203 RMVar_ID_19203 Human_SNP_ID_689207507 A-to-I Human chr21 + 16490504 16490504 16490504 AGTGTAAGAAAAGAAAGTAATCGGCAGGGCACAGTGGCTCACACCTGTAATCCTAGTACTTTGGA AGTGTAAGAAAAGAAAGTAATCGGCAGGGCACGGTGGCTCACACCTGTAATCCTAGTACTTTGGA A G MIR99AHG Ensembl:ENSG00000215386 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1160225917 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_349730,RMVar_hsa_circ_352145 19204 RMVar_ID_19204 Human_SNP_ID_689211659 A-to-I Human chr21 + 16508384 16508383 16508385 CACCACGCCCAGCTAATTTTTGTGTCTTTAGTAGAGAGAGGATTTCACCATGTTGCCCAGGCTAG CACCACGCCCAGCTAATTTTTGTGTCTTTAGT__AGAGAGGATTTCACCATGTTGCCCAGGCTAG TAG T MIR99AHG Ensembl:ENSG00000215386 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs947496914 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_349730,RMVar_hsa_circ_352145 19205 RMVar_ID_19205 Human_SNP_ID_689238092 A-to-I Human chr21 + 16613652 16613652 16613652 TCGACTCCTGGCTGGTCTCGACTCCTGACCTCAGGTGATCCACCTACCTCGGCCTCTCAAAGTGT TCGACTCCTGGCTGGTCTCGACTCCTGACCTCGGGTGATCCACCTACCTCGGCCTCTCAAAGTGT A G MIR99AHG Ensembl:ENSG00000215386 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1469666215 Functional Loss SNV dbSNP153 33..33 33 - - - 19206 RMVar_ID_19206 Human_SNP_ID_689239137 A-to-I Human chr21 + 16616789 16616789 16616789 TATTTTTAGTAGAGACGGGATTTCGCCGTGTTAGCCAGAATGATCTCGATCTCCTGACCTCGTGA TATTTTTAGTAGAGACGGGATTTCGCCGTGTTGGCCAGAATGATCTCGATCTCCTGACCTCGTGA A G MIR99AHG Ensembl:ENSG00000215386 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1487237887 Functional Loss SNV dbSNP153 33..33 33 - - - 19207 RMVar_ID_19207 Human_SNP_ID_689501720 A-to-I Human chr21 - 17502942 17502942 17502942 TGCCATGCCCAGCTGATATTTTGTATTTTAGTAGAGATGGGGTTTCACCATATTGGCCAGGCTGG TGCCATGCCCAGCTGATATTTTGTATTTTAGTGGAGATGGGGTTTCACCATATTGGCCAGGCTGG T C lnc-BTG3-5,lnc-BTG3-6,lnc-BTG3-6:2,lnc-BTG3-5:2,lnc-BTG3-6:3 RNACentral:URS00008BB5B9,RNACentral:URS0000D5BA91,RNACentral:URS0000D5C8E2,RNACentral:URS00008B64F6,RNACentral:URS00008BC522 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1159476496 Functional Loss SNV dbSNP153 33..33 33 - - - 19208 RMVar_ID_19208 Human_SNP_ID_689510820 A-to-I Human chr21 + 17535792 17535792 17535792 ATTTTGATAGCCCCAGGCAGGTGGATCGCCTGAGTTCGGGAGTTCAAGACCAGCCTGAATAACAC ATTTTGATAGCCCCAGGCAGGTGGATCGCCTGGGTTCGGGAGTTCAAGACCAGCCTGAATAACAC A G CXADR Ensembl:ENSG00000154639 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs977439425 Functional Loss SNV dbSNP153 33..33 33 - - - 19209 RMVar_ID_19209 Human_SNP_ID_689575122 A-to-I Human chr21 - 17790659 17790659 17790659 TTTAAAAGGCATGCACTTGAGACTCCAGTAATAGATGATTCAGGCAGCAGAATAGTGTTTTGTTG TTTAAAAGGCATGCACTTGAGACTCCAGTAATGGATGATTCAGGCAGCAGAATAGTGTTTTGTTG T C C21orf91,C21orf91-OT1 Ensembl:ENSG00000154642,Ensembl:ENSG00000240770 Protein coding,lincRNA 3'UTR,intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1006082208 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7029971,Human_RBP_ID_8206968,Human_RBP_ID_9120540,Human_RBP_ID_14200648,Human_RBP_ID_17513155 19210 RMVar_ID_19210 Human_SNP_ID_201027514 A-to-I Human chr4 - 120057975 120057975 120057975 GGGCGCATCTCAGCTACTTGGGAGGCTGAGGCAGGAGAAATCGCTTGAACCCATGAGGTGGAGGT GGGCGCATCTCAGCTACTTGGGAGGCTGAGGCGGGAGAAATCGCTTGAACCCATGAGGTGGAGGT T C MAD2L1 Ensembl:ENSG00000164109 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1440358812 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26513010 19211 RMVar_ID_19211 Human_SNP_ID_201027663 A-to-I Human chr4 - 120058587 120058587 120058587 TCTTATTCTGTCGCCCAGGCTGGAGTACAGTGACGCAGCTCAGCTCACTACAGCCTCTGCCTCCC TCTTATTCTGTCGCCCAGGCTGGAGTACAGTGGCGCAGCTCAGCTCACTACAGCCTCTGCCTCCC T C MAD2L1 Ensembl:ENSG00000164109 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1453955689 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15034972 19212 RMVar_ID_19212 Human_SNP_ID_201215252 A-to-I Human chr4 - 120832134 120832134 120832134 CTCTTTCCTTTATAAATATCCTAGTCTCAGGTATTTCTTCATAGCAGCGTGAGAATGGACTAATA CTCTTTCCTTTATAAATATCCTAGTCTCAGGTGTTTCTTCATAGCAGCGTGAGAATGGACTAATA T C PRDM5 Ensembl:ENSG00000138738 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs964215739 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_53183,RMVar_hsa_circ_23069,RMVar_hsa_circ_112373,RMVar_hsa_circ_228330,RMVar_hsa_circ_376748,RMVar_hsa_circ_348212 19213 RMVar_ID_19213 Human_SNP_ID_201348616 A-to-I Human chr4 - 121370161 121370161 121370161 CAGCATCCCTTGGAAGCCAGTGATTTCAGAGCACAAGTATCAGCACCTCACCAAGGTGGAGGAAG CAGCATCCCTTGGAAGCCAGTGATTTCAGAGCTCAAGTATCAGCACCTCACCAAGGTGGAGGAAG T A AC093816.1,QRFPR Ensembl:ENSG00000213480,Ensembl:ENSG00000186867 Pseudogene,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1329682209 Functional Loss SNV dbSNP153 33..33 33 - - - 19214 RMVar_ID_19214 Human_SNP_ID_201452838 A-to-I Human chr4 + 121807215 121807215 121807215 GGGAGGCTGACATAGGAGAATCGCATGAGCCCAGGAGGCGGAGGTTGCCGGGAGCTGACATCTTG GGGAGGCTGACATAGGAGAATCGCATGAGCCCGGGAGGCGGAGGTTGCCGGGAGCTGACATCTTG A G EXOSC9 Ensembl:ENSG00000123737 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1047777161 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15036100 RMVar_hsa_circ_41201,RMVar_hsa_circ_23960,RMVar_hsa_circ_265152,RMVar_hsa_circ_123955,RMVar_hsa_circ_275259,RMVar_hsa_circ_275406,RMVar_hsa_circ_228344,RMVar_hsa_circ_228346,RMVar_hsa_circ_228345 19215 RMVar_ID_19215 Human_SNP_ID_201455484 A-to-I Human chr4 - 121816978 121816978 121816978 GTTTATTATTTTAAAGCACATTAAAAACAAAAAACTATTTTTAAAATCCTGCTAGATTTTATAAT GTTTATTATTTTAAAGCACATTAAAAACAAAATACTATTTTTAAAATCCTGCTAGATTTTATAAT T A CCNA2 Ensembl:ENSG00000145386 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1433417085 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17293555,Human_RBP_ID_17407095,Human_RBP_ID_17522344,Human_RBP_ID_17705078,Human_RBP_ID_18017524 Human_miRNA_ID_185391 RMVar_hsa_circ_89454,RMVar_hsa_circ_228352 19216 RMVar_ID_19216 Human_SNP_ID_201464740 A-to-I Human chr4 - 121856625 121856625 121856625 TCACTGCGACCTCTGCTTCCCGGGTTCAAGCAATTCTCCTCCTTTAGCCTCCTGAGTAGCTGGGA TCACTGCGACCTCTGCTTCCCGGGTTCAAGCAGTTCTCCTCCTTTAGCCTCCTGAGTAGCTGGGA T C BBS7 Ensembl:ENSG00000138686 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1277306217 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70727,RMVar_hsa_circ_228368,RMVar_hsa_circ_77755,RMVar_hsa_circ_105060,RMVar_hsa_circ_228369 19217 RMVar_ID_19217 Human_SNP_ID_201563596 A-to-I Human chr4 + 122277230 122277230 122277230 GGGCATGGTGGCACGTCTCTGTAGTCCCAGCCACTTGAGAGACTGAGTTGGGAGGATCACTTGAG GGGCATGGTGGCACGTCTCTGTAGTCCCAGCCGCTTGAGAGACTGAGTTGGGAGGATCACTTGAG A G KIAA1109 Ensembl:ENSG00000138688 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs896519515 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_138,RMVar_hsa_circ_6346,RMVar_hsa_circ_116232,RMVar_hsa_circ_228376,RMVar_hsa_circ_103362,RMVar_hsa_circ_228396,RMVar_hsa_circ_95767,RMVar_hsa_circ_119351,RMVar_hsa_circ_228397,RMVar_hsa_circ_94844,RMVar_hsa_circ_228398,RMVar_hsa_circ_58172,RMVar_hsa_circ_228401,RMVar_hsa_circ_93496,RMVar_hsa_circ_228402,RMVar_hsa_circ_12999,RMVar_hsa_circ_68422,RMVar_hsa_circ_67919,RMVar_hsa_circ_57229,RMVar_hsa_circ_72305,RMVar_hsa_circ_40866,RMVar_hsa_circ_42685,RMVar_hsa_circ_362827,RMVar_hsa_circ_364458,RMVar_hsa_circ_52699,RMVar_hsa_circ_25734,RMVar_hsa_circ_78218,RMVar_hsa_circ_52223,RMVar_hsa_circ_340741,RMVar_hsa_circ_367970,RMVar_hsa_circ_228412,RMVar_hsa_circ_364211,RMVar_hsa_circ_27084,RMVar_hsa_circ_95123,RMVar_hsa_circ_228413,RMVar_hsa_circ_228414,RMVar_hsa_circ_228415 19218 RMVar_ID_19218 Human_SNP_ID_201713915 A-to-I Human chr4 - 122919490 122919490 122919490 TCAGTTTTGGCCAGGCGCGGTGGGTCACGCCTATAATCCCAGCACTTTGGGAGGCCGAGGCGGGC TCAGTTTTGGCCAGGCGCGGTGGGTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGC T C NUDT6 Ensembl:ENSG00000170917 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs563092270 Functional Loss SNV dbSNP153 33..33 33 - - - 19219 RMVar_ID_19219 Human_SNP_ID_201713916 A-to-I Human chr4 - 122919490 122919490 122919490 TCAGTTTTGGCCAGGCGCGGTGGGTCACGCCTATAATCCCAGCACTTTGGGAGGCCGAGGCGGGC TCAGTTTTGGCCAGGCGCGGTGGGTCACGCCTCTAATCCCAGCACTTTGGGAGGCCGAGGCGGGC T G NUDT6 Ensembl:ENSG00000170917 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs563092270 Functional Loss SNV dbSNP153 33..33 33 - - - 19220 RMVar_ID_19220 Human_SNP_ID_201779114 A-to-I Human chr4 + 123187955 123187951 123187956 GGGAGGTTGAGGCTGCAGTGAGCCATGATCATACCACTGTACTTTAGCCTAGGTGACAGAGTGAG GGGAGGTTGAGGCTGCAGTGAGCCATGAT_____CACTGTACTTTAGCCTAGGTGACAGAGTGAG TCATAC T SPATA5 Ensembl:ENSG00000145375 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1403041470 Functional Loss DEL dbSNP153 30..34 33 - - - RMVar_hsa_circ_93814,RMVar_hsa_circ_114038,RMVar_hsa_circ_228444,RMVar_hsa_circ_108014,RMVar_hsa_circ_113238,RMVar_hsa_circ_228447,RMVar_hsa_circ_228446,RMVar_hsa_circ_228457 19221 RMVar_ID_19221 Human_SNP_ID_201780718 A-to-I Human chr4 + 123195275 123195275 123195275 ATACTATCCACGCTATCCAAGTTTACCTGGATAAATAGAATGCAATCAGAATTATGTTGAAGCTA ATACTATCCACGCTATCCAAGTTTACCTGGATGAATAGAATGCAATCAGAATTATGTTGAAGCTA A G SPATA5 Ensembl:ENSG00000145375 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1216344602 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93814,RMVar_hsa_circ_114038,RMVar_hsa_circ_228444,RMVar_hsa_circ_108014,RMVar_hsa_circ_113238,RMVar_hsa_circ_228447,RMVar_hsa_circ_228446,RMVar_hsa_circ_228457 19222 RMVar_ID_19222 Human_SNP_ID_201781451 A-to-I Human chr4 + 123198087 123198087 123198087 GGTCAGGAGTTCAAGACCAGCCTGGCGAACACAGTGAAATCCCGTATCTGCTAAAATTACAAAAA GGTCAGGAGTTCAAGACCAGCCTGGCGAACACGGTGAAATCCCGTATCTGCTAAAATTACAAAAA A G SPATA5 Ensembl:ENSG00000145375 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1442150194 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93814,RMVar_hsa_circ_114038,RMVar_hsa_circ_228444,RMVar_hsa_circ_108014,RMVar_hsa_circ_113238,RMVar_hsa_circ_228447,RMVar_hsa_circ_228446,RMVar_hsa_circ_228457 19223 RMVar_ID_19223 Human_SNP_ID_201782493 A-to-I Human chr4 + 123202902 123202902 123202902 TGTCACAGCTGGGCACGATGGCTTGCATCTGTAGTCCTAGCTACTCGGGAGGCTGGGGTGGGAGG TGTCACAGCTGGGCACGATGGCTTGCATCTGTTGTCCTAGCTACTCGGGAGGCTGGGGTGGGAGG A T SPATA5 Ensembl:ENSG00000145375 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1398259931 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93814,RMVar_hsa_circ_114038,RMVar_hsa_circ_228444,RMVar_hsa_circ_108014,RMVar_hsa_circ_113238,RMVar_hsa_circ_228447,RMVar_hsa_circ_228446,RMVar_hsa_circ_228457 19224 RMVar_ID_19224 Human_SNP_ID_201807131 A-to-I Human chr4 + 123315197 123315196 123315197 AAAGATAGGCCAAATTGTACTTTTTTTTTTTTATGAGACAGAGTCTCGCTGCTCTGTCGCCCAGG AAAGATAGGCCAAATTGTACTTTTTTTTTTTT_TGAGACAGAGTCTCGCTGCTCTGTCGCCCAGG TA T SPATA5 Ensembl:ENSG00000145375 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1208150769 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_4772029,Human_RBP_ID_15040820,Human_RBP_ID_24500143 RMVar_hsa_circ_108014,RMVar_hsa_circ_228446,RMVar_hsa_circ_266991 19225 RMVar_ID_19225 Human_SNP_ID_201807133 A-to-I Human chr4 + 123315197 123315197 123315197 AAAGATAGGCCAAATTGTACTTTTTTTTTTTTATGAGACAGAGTCTCGCTGCTCTGTCGCCCAGG AAAGATAGGCCAAATTGTACTTTTTTTTTTTTTTGAGACAGAGTCTCGCTGCTCTGTCGCCCAGG A T SPATA5 Ensembl:ENSG00000145375 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355808017 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4772029,Human_RBP_ID_15040820,Human_RBP_ID_24500143 RMVar_hsa_circ_108014,RMVar_hsa_circ_228446,RMVar_hsa_circ_266991 19226 RMVar_ID_19226 Human_SNP_ID_201807926 A-to-I Human chr4 + 123318747 123318747 123318747 AGGAGTTTGAATCCAGCCTGGTCAATGTAGCGAGATCCTATCTCTTAAAAAAAAAAAAAAAAGGG AGGAGTTTGAATCCAGCCTGGTCAATGTAGCGGGATCCTATCTCTTAAAAAAAAAAAAAAAAGGG A G SPATA5 Ensembl:ENSG00000145375 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474342596 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26518482 RMVar_hsa_circ_108014,RMVar_hsa_circ_228446,RMVar_hsa_circ_266991 19227 RMVar_ID_19227 Human_SNP_ID_201807930 A-to-I Human chr4 + 123318754 123318752 123318754 TGAATCCAGCCTGGTCAATGTAGCGAGATCCTATCTCTTAAAAAAAAAAAAAAAAGGGGGGAACA TGAATCCAGCCTGGTCAATGTAGCGAGATCC__TCTCTTAAAAAAAAAAAAAAAAGGGGGGAACA CTA C SPATA5 Ensembl:ENSG00000145375 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1188236550 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_108014,RMVar_hsa_circ_228446,RMVar_hsa_circ_266991 19228 RMVar_ID_19228 Human_SNP_ID_201894815 A-to-I Human chr4 + 123680649 123680649 123680649 CCCCGTCTCTACTAAAAATACAAAAATTAGCCAAGCATGGTGGCACACGCCTGTAATCCCAGCTA CCCCGTCTCTACTAAAAATACAAAAATTAGCCGAGCATGGTGGCACACGCCTGTAATCCCAGCTA A G LINC01091 Ensembl:ENSG00000249464 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs906857924 Functional Loss SNV dbSNP153 33..33 33 - - - 19229 RMVar_ID_19229 Human_SNP_ID_201894816 A-to-I Human chr4 + 123680653 123680653 123680653 GTCTCTACTAAAAATACAAAAATTAGCCAAGCATGGTGGCACACGCCTGTAATCCCAGCTACTCT GTCTCTACTAAAAATACAAAAATTAGCCAAGCGTGGTGGCACACGCCTGTAATCCCAGCTACTCT A G LINC01091 Ensembl:ENSG00000249464 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1399235429 Functional Loss SNV dbSNP153 33..33 33 - - - 19230 RMVar_ID_19230 Human_SNP_ID_202127572 A-to-I Human chr4 - 124659524 124659524 124659524 TCAAGTGATCTTCCTTGGCCTCCCAAAGTGCTAGGATTACAGACATGAGCCACTACACCTGGCCT TCAAGTGATCTTCCTTGGCCTCCCAAAGTGCTGGGATTACAGACATGAGCCACTACACCTGGCCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1043037301 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_228463 19231 RMVar_ID_19231 Human_SNP_ID_202866328 A-to-I Human chr4 + 127659127 127659127 127659127 TCAGGCAATAATGTGAGTGATGGGGAGTGGCTATAAATATGAATGAAGCTTCGCTCACTGGCCAC TCAGGCAATAATGTGAGTGATGGGGAGTGGCTGTAAATATGAATGAAGCTTCGCTCACTGGCCAC A G INTU Ensembl:ENSG00000164066 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1024320325 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_228492,RMVar_hsa_circ_267671,RMVar_hsa_circ_272662,RMVar_hsa_circ_327352,RMVar_hsa_circ_271026,RMVar_hsa_circ_41279,RMVar_hsa_circ_228490,RMVar_hsa_circ_228491,RMVar_hsa_circ_228489,RMVar_hsa_circ_19069,RMVar_hsa_circ_333852,RMVar_hsa_circ_228493 19232 RMVar_ID_19232 Human_SNP_ID_202880018 A-to-I Human chr4 + 127716462 127716462 127716462 CTTGTAGCTGTGCTTTCTTGATGCGTAGAAACACGTGCATGGAGGATCAAACACTGTCAGAATTG CTTGTAGCTGTGCTTTCTTGATGCGTAGAAACGCGTGCATGGAGGATCAAACACTGTCAGAATTG A G INTU Ensembl:ENSG00000164066 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1560623867 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15041767 19233 RMVar_ID_19233 Human_SNP_ID_202900979 A-to-I Human chr4 - 127809401 127809401 127809401 CAAATGCAGAGTCTTGAGTTATGAAGTATCCAAATGAATGTGCATGAGCATGCTGCAAAGCTGCC CAAATGCAGAGTCTTGAGTTATGAAGTATCCACATGAATGTGCATGAGCATGCTGCAAAGCTGCC T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs895147975 Functional Loss SNV dbSNP153 33..33 33 - - - 19234 RMVar_ID_19234 Human_SNP_ID_202906875 A-to-I Human chr4 + 127835424 127835424 127835424 TAGCAGTAATGTAAAATTATTAAGTTTTGGCCAGGCGCTGTGGCTCACGCCTGTAATCCTAGCAC TAGCAGTAATGTAAAATTATTAAGTTTTGGCCTGGCGCTGTGGCTCACGCCTGTAATCCTAGCAC A T HSPA4L Ensembl:ENSG00000164070 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs906791808 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26518485 19235 RMVar_ID_19235 Human_SNP_ID_202906925 A-to-I Human chr4 + 127835690 127835690 127835690 GTGCTCCTGCACTCCAGCCTGGGCAACAGAACAAGACTCCGTCTCAAAAAAAAAACAAAAATTCT GTGCTCCTGCACTCCAGCCTGGGCAACAGAACGAGACTCCGTCTCAAAAAAAAAACAAAAATTCT A G HSPA4L Ensembl:ENSG00000164070 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1330208468 Functional Loss SNV dbSNP153 33..33 33 - - - 19236 RMVar_ID_19236 Human_SNP_ID_202906966 A-to-I Human chr4 + 127835812 127835812 127835812 TTGATTTTGAAAAGGATAACAAGGCTGGGCACAGTGACTCACACCTGTAATCCTAGCACTTTGAG TTGATTTTGAAAAGGATAACAAGGCTGGGCACGGTGACTCACACCTGTAATCCTAGCACTTTGAG A G HSPA4L Ensembl:ENSG00000164070 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs988662418 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15042180,Human_RBP_ID_26518486 19237 RMVar_ID_19237 Human_SNP_ID_202906973 A-to-I Human chr4 + 127835850 127835850 127835850 TCACACCTGTAATCCTAGCACTTTGAGAGGCTAAGAAGGGAGGATCACTTGAACCCAGGAGTTCA TCACACCTGTAATCCTAGCACTTTGAGAGGCTGAGAAGGGAGGATCACTTGAACCCAGGAGTTCA A G HSPA4L Ensembl:ENSG00000164070 Protein coding 3'UTR GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs541219534 Functional Loss SNV dbSNP153 33..33 33 - - - 19238 RMVar_ID_19238 Human_SNP_ID_202907335 A-to-I Human chr4 + 127836996 127836996 127836996 AGAGTATGGCTTTGTTACCCAGGCTGGATTGCAATGGGGTGATCTAGGCTCACTGCAGCCTCCAC AGAGTATGGCTTTGTTACCCAGGCTGGATTGCGATGGGGTGATCTAGGCTCACTGCAGCCTCCAC A G HSPA4L Ensembl:ENSG00000164070 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1390214050 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26518488 19239 RMVar_ID_19239 Human_SNP_ID_202907366 A-to-I Human chr4 + 127837125 127837125 127837125 ACACCACACCCAGCTAATTTTTGTATTTTTATAGAGATGGAGTTTTGCCATGTTGGCCAGCCTGG ACACCACACCCAGCTAATTTTTGTATTTTTATGGAGATGGAGTTTTGCCATGTTGGCCAGCCTGG A G HSPA4L Ensembl:ENSG00000164070 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs961620565 Functional Loss SNV dbSNP153 33..33 33 - - - 19240 RMVar_ID_19240 Human_SNP_ID_202907532 A-to-I Human chr4 + 127837835 127837835 127837835 TTTGTTTTTGTTTTTTTTTTGGAAACAGTCTCACTCTGTCACCCAGGCTGGAGGGCACAATCTCT TTTGTTTTTGTTTTTTTTTTGGAAACAGTCTCCCTCTGTCACCCAGGCTGGAGGGCACAATCTCT A C HSPA4L Ensembl:ENSG00000164070 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973398579 Functional Loss SNV dbSNP153 33..33 33 - - - 19241 RMVar_ID_19241 Human_SNP_ID_202907536 A-to-I Human chr4 + 127837861 127837861 127837861 AGTCTCACTCTGTCACCCAGGCTGGAGGGCACAATCTCTGCTCACTGCAACCTCCACCTCCTGGG AGTCTCACTCTGTCACCCAGGCTGGAGGGCACTATCTCTGCTCACTGCAACCTCCACCTCCTGGG A T HSPA4L Ensembl:ENSG00000164070 Protein coding 3'UTR GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs1204175463 Functional Loss SNV dbSNP153 33..33 33 - - - 19242 RMVar_ID_19242 Human_SNP_ID_202907558 A-to-I Human chr4 + 127837970 127837970 127837970 GGGATTACAGGAACCCACCACCACGCCCAGCTAATTTTTGTATTTTTAGTAGATGGGGTTTCATC GGGATTACAGGAACCCACCACCACGCCCAGCTCATTTTTGTATTTTTAGTAGATGGGGTTTCATC A C HSPA4L Ensembl:ENSG00000164070 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404752350 Functional Loss SNV dbSNP153 33..33 33 - - - 19243 RMVar_ID_19243 Human_SNP_ID_202908043 A-to-I Human chr4 + 127840100 127840096 127840100 AAATTAGCGGGGCCATGGTGACGTGCACCTGTAATCCCAGCTACTCGGGAGGCTGAGGTGGGAGA AAATTAGCGGGGCCATGGTGACGTGCACC____ATCCCAGCTACTCGGGAGGCTGAGGTGGGAGA CTGTA C HSPA4L Ensembl:ENSG00000164070 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs950939767 Functional Loss DEL dbSNP153 30..33 33 - - - 19244 RMVar_ID_19244 Human_SNP_ID_202910953 A-to-I Human chr4 - 127853403 127853403 127853403 ACATGCCTGTAGTCCCAGCTACTTGGGAGGCTAAGGATGGAGGATCACTTGAGCTCAGGAGGTCA ACATGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGATGGAGGATCACTTGAGCTCAGGAGGTCA T C lnc-MFSD8-12,lnc-MFSD8-12:2 RNACentral:URS0000D5CF5D,RNACentral:URS0000D57B5E lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1210781117 Functional Loss SNV dbSNP153 33..33 33 - - - 19245 RMVar_ID_19245 Human_SNP_ID_202933355 A-to-I Human chr4 - 127941525 127941525 127941525 CTCGGAGGCAGAGGTTGCAGTGAGCTGAGATCACATCATTGCACTCCAGCTTGGGCAACAAGCGC CTCGGAGGCAGAGGTTGCAGTGAGCTGAGATCCCATCATTGCACTCCAGCTTGGGCAACAAGCGC T G MFSD8 Ensembl:ENSG00000164073 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs540342087 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21478,RMVar_hsa_circ_316689,RMVar_hsa_circ_87611,RMVar_hsa_circ_228522,RMVar_hsa_circ_356938,RMVar_hsa_circ_324033,RMVar_hsa_circ_279950,RMVar_hsa_circ_228525,RMVar_hsa_circ_56324,RMVar_hsa_circ_228526,RMVar_hsa_circ_285275,RMVar_hsa_circ_228527,RMVar_hsa_circ_352268,RMVar_hsa_circ_228529,RMVar_hsa_circ_333181,RMVar_hsa_circ_264921,RMVar_hsa_circ_228531 19246 RMVar_ID_19246 Human_SNP_ID_202933735 A-to-I Human chr4 - 127943105 127943104 127943105 TCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCGTCTGCCACTGCACCTG TCAAGCAATTCTCCTGCCTCAGCCTCCCGAGT_GCTGGGATTACAGGCGTCTGCCACTGCACCTG CT C MFSD8 Ensembl:ENSG00000164073 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1370073855 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_21478,RMVar_hsa_circ_87611,RMVar_hsa_circ_228522,RMVar_hsa_circ_356938,RMVar_hsa_circ_324033,RMVar_hsa_circ_56324,RMVar_hsa_circ_228526,RMVar_hsa_circ_95675,RMVar_hsa_circ_285275,RMVar_hsa_circ_228527,RMVar_hsa_circ_352268,RMVar_hsa_circ_228529,RMVar_hsa_circ_333181,RMVar_hsa_circ_264921,RMVar_hsa_circ_228531,RMVar_hsa_circ_358815,RMVar_hsa_circ_359772,RMVar_hsa_circ_343473,RMVar_hsa_circ_228532,RMVar_hsa_circ_228534,RMVar_hsa_circ_228535,RMVar_hsa_circ_228533 19247 RMVar_ID_19247 Human_SNP_ID_202944542 A-to-I Human chr4 + 127987089 127987089 127987089 AATAATTAATAATGGGCTGGGTGCCGTGCCTCACACCTGTAATATCAGCACTTTGGGAGGCCGAG AATAATTAATAATGGGCTGGGTGCCGTGCCTCCCACCTGTAATATCAGCACTTTGGGAGGCCGAG A C ABHD18 Ensembl:ENSG00000164074 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1039652835 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6941,RMVar_hsa_circ_279023,RMVar_hsa_circ_288390,RMVar_hsa_circ_337031,RMVar_hsa_circ_300769,RMVar_hsa_circ_287896,RMVar_hsa_circ_279487,RMVar_hsa_circ_44971,RMVar_hsa_circ_65787,RMVar_hsa_circ_13565,RMVar_hsa_circ_228537,RMVar_hsa_circ_228539,RMVar_hsa_circ_228541,RMVar_hsa_circ_228542,RMVar_hsa_circ_228540,RMVar_hsa_circ_228538,RMVar_hsa_circ_228544,RMVar_hsa_circ_277187 19248 RMVar_ID_19248 Human_SNP_ID_202945694 A-to-I Human chr4 + 127992354 127992352 127992354 AAATTTAGCCAGGCATGGTGGCAGACATCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA AAATTTAGCCAGGCATGGTGGCAGACATCTG__ATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA GTA G ABHD18 Ensembl:ENSG00000164074 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1560854630 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_6941,RMVar_hsa_circ_279023,RMVar_hsa_circ_288390,RMVar_hsa_circ_337031,RMVar_hsa_circ_300769,RMVar_hsa_circ_287896,RMVar_hsa_circ_44971,RMVar_hsa_circ_65787,RMVar_hsa_circ_13565,RMVar_hsa_circ_228537,RMVar_hsa_circ_228539,RMVar_hsa_circ_228541,RMVar_hsa_circ_228540,RMVar_hsa_circ_228538,RMVar_hsa_circ_127907,RMVar_hsa_circ_356721,RMVar_hsa_circ_369134,RMVar_hsa_circ_228545,RMVar_hsa_circ_228546 19249 RMVar_ID_19249 Human_SNP_ID_202948041 A-to-I Human chr4 + 128002721 128002721 128002721 GCTGGAGTACAGTGGCGTGATCTGGGCTCACGACAAGCCCTGTCTCCTGAGTTCAAGTGATTCTT GCTGGAGTACAGTGGCGTGATCTGGGCTCACGGCAAGCCCTGTCTCCTGAGTTCAAGTGATTCTT A G ABHD18 Ensembl:ENSG00000164074 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1176843305 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6941,RMVar_hsa_circ_279023,RMVar_hsa_circ_288390,RMVar_hsa_circ_337031,RMVar_hsa_circ_300769,RMVar_hsa_circ_287896,RMVar_hsa_circ_65787,RMVar_hsa_circ_13565,RMVar_hsa_circ_38832,RMVar_hsa_circ_228537,RMVar_hsa_circ_228539,RMVar_hsa_circ_228541,RMVar_hsa_circ_228540,RMVar_hsa_circ_228538,RMVar_hsa_circ_127907,RMVar_hsa_circ_356721,RMVar_hsa_circ_369134,RMVar_hsa_circ_228545,RMVar_hsa_circ_228546,RMVar_hsa_circ_321824,RMVar_hsa_circ_228547 19250 RMVar_ID_19250 Human_SNP_ID_202949888 A-to-I Human chr4 + 128010449 128010449 128010449 TACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCCAGGAGACAGGTTGCAGTGAGCCAAGATC TACTCAGGAGGCTGAGGCAGGAGAATCACTTGGACCCAGGAGACAGGTTGCAGTGAGCCAAGATC A G ABHD18 Ensembl:ENSG00000164074 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1487132470 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6941,RMVar_hsa_circ_279023,RMVar_hsa_circ_288390,RMVar_hsa_circ_337031,RMVar_hsa_circ_300769,RMVar_hsa_circ_287896,RMVar_hsa_circ_38832,RMVar_hsa_circ_228537,RMVar_hsa_circ_228539,RMVar_hsa_circ_228540,RMVar_hsa_circ_228538,RMVar_hsa_circ_356721,RMVar_hsa_circ_369134,RMVar_hsa_circ_228546,RMVar_hsa_circ_321824,RMVar_hsa_circ_228549,RMVar_hsa_circ_307927,RMVar_hsa_circ_326565,RMVar_hsa_circ_228547,RMVar_hsa_circ_308891,RMVar_hsa_circ_68990,RMVar_hsa_circ_305903,RMVar_hsa_circ_228550,RMVar_hsa_circ_228551,RMVar_hsa_circ_228548 19251 RMVar_ID_19251 Human_SNP_ID_202949955 A-to-I Human chr4 + 128010759 128010752 128010760 AACATGGCAAAACCCCTATCTCTACTAAAAATACAAAAATTAGCCAGGCGTGGTGGCGTGTGCCT AACATGGCAAAACCCCTATCTCTACT________AAAAATTAGCCAGGCGTGGTGGCGTGTGCCT TAAAAATAC T ABHD18 Ensembl:ENSG00000164074 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1356303186 Functional Loss DEL dbSNP153 27..34 33 - - - RMVar_hsa_circ_6941,RMVar_hsa_circ_279023,RMVar_hsa_circ_288390,RMVar_hsa_circ_337031,RMVar_hsa_circ_300769,RMVar_hsa_circ_287896,RMVar_hsa_circ_38832,RMVar_hsa_circ_228537,RMVar_hsa_circ_228539,RMVar_hsa_circ_228540,RMVar_hsa_circ_228538,RMVar_hsa_circ_356721,RMVar_hsa_circ_369134,RMVar_hsa_circ_228546,RMVar_hsa_circ_321824,RMVar_hsa_circ_228549,RMVar_hsa_circ_307927,RMVar_hsa_circ_326565,RMVar_hsa_circ_228547,RMVar_hsa_circ_308891,RMVar_hsa_circ_68990,RMVar_hsa_circ_305903,RMVar_hsa_circ_228550,RMVar_hsa_circ_228551,RMVar_hsa_circ_228548 19252 RMVar_ID_19252 Human_SNP_ID_202949999 A-to-I Human chr4 + 128010892 128010892 128010892 AGCCGCCTGCACTCCAGCCTGGGCGACGGAGCAAGACTGCGCCTCAAAAAAAAAAAAAAAAAACC AGCCGCCTGCACTCCAGCCTGGGCGACGGAGCGAGACTGCGCCTCAAAAAAAAAAAAAAAAAACC A G ABHD18 Ensembl:ENSG00000164074 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1473050908 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6941,RMVar_hsa_circ_279023,RMVar_hsa_circ_288390,RMVar_hsa_circ_337031,RMVar_hsa_circ_300769,RMVar_hsa_circ_287896,RMVar_hsa_circ_38832,RMVar_hsa_circ_228537,RMVar_hsa_circ_228539,RMVar_hsa_circ_228540,RMVar_hsa_circ_228538,RMVar_hsa_circ_356721,RMVar_hsa_circ_369134,RMVar_hsa_circ_228546,RMVar_hsa_circ_321824,RMVar_hsa_circ_228549,RMVar_hsa_circ_307927,RMVar_hsa_circ_326565,RMVar_hsa_circ_228547,RMVar_hsa_circ_308891,RMVar_hsa_circ_68990,RMVar_hsa_circ_305903,RMVar_hsa_circ_228550,RMVar_hsa_circ_228551,RMVar_hsa_circ_228548 19253 RMVar_ID_19253 Human_SNP_ID_202950117 A-to-I Human chr4 + 128011288 128011288 128011288 CTCCTGCCTCAGCCTCCCGCGTAGCTGACACTACAGGCGCCCGCCACCTCGCCCAGCTAATTTTT CTCCTGCCTCAGCCTCCCGCGTAGCTGACACTGCAGGCGCCCGCCACCTCGCCCAGCTAATTTTT A G ABHD18 Ensembl:ENSG00000164074 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1183951858 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6941,RMVar_hsa_circ_279023,RMVar_hsa_circ_288390,RMVar_hsa_circ_337031,RMVar_hsa_circ_300769,RMVar_hsa_circ_287896,RMVar_hsa_circ_38832,RMVar_hsa_circ_228537,RMVar_hsa_circ_228539,RMVar_hsa_circ_228540,RMVar_hsa_circ_228538,RMVar_hsa_circ_356721,RMVar_hsa_circ_369134,RMVar_hsa_circ_228546,RMVar_hsa_circ_321824,RMVar_hsa_circ_228549,RMVar_hsa_circ_307927,RMVar_hsa_circ_326565,RMVar_hsa_circ_228547,RMVar_hsa_circ_308891,RMVar_hsa_circ_68990,RMVar_hsa_circ_305903,RMVar_hsa_circ_228550,RMVar_hsa_circ_228551,RMVar_hsa_circ_228548 19254 RMVar_ID_19254 Human_SNP_ID_202950128 A-to-I Human chr4 + 128011310 128011310 128011310 AGCTGACACTACAGGCGCCCGCCACCTCGCCCAGCTAATTTTTTGTATTTTTAGTAGTGATGGGG AGCTGACACTACAGGCGCCCGCCACCTCGCCCGGCTAATTTTTTGTATTTTTAGTAGTGATGGGG A G ABHD18 Ensembl:ENSG00000164074 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs984676570 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6941,RMVar_hsa_circ_279023,RMVar_hsa_circ_288390,RMVar_hsa_circ_337031,RMVar_hsa_circ_300769,RMVar_hsa_circ_287896,RMVar_hsa_circ_38832,RMVar_hsa_circ_228537,RMVar_hsa_circ_228539,RMVar_hsa_circ_228540,RMVar_hsa_circ_228538,RMVar_hsa_circ_356721,RMVar_hsa_circ_369134,RMVar_hsa_circ_228546,RMVar_hsa_circ_321824,RMVar_hsa_circ_228549,RMVar_hsa_circ_307927,RMVar_hsa_circ_326565,RMVar_hsa_circ_228547,RMVar_hsa_circ_308891,RMVar_hsa_circ_68990,RMVar_hsa_circ_305903,RMVar_hsa_circ_228550,RMVar_hsa_circ_228551,RMVar_hsa_circ_228548 19255 RMVar_ID_19255 Human_SNP_ID_202950131 A-to-I Human chr4 + 128011330 128011330 128011330 GCCACCTCGCCCAGCTAATTTTTTGTATTTTTAGTAGTGATGGGGTTTCACCATGTTAGCCAGGA GCCACCTCGCCCAGCTAATTTTTTGTATTTTTCGTAGTGATGGGGTTTCACCATGTTAGCCAGGA A C ABHD18 Ensembl:ENSG00000164074 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1320706713 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6941,RMVar_hsa_circ_279023,RMVar_hsa_circ_288390,RMVar_hsa_circ_337031,RMVar_hsa_circ_300769,RMVar_hsa_circ_287896,RMVar_hsa_circ_38832,RMVar_hsa_circ_228537,RMVar_hsa_circ_228539,RMVar_hsa_circ_228540,RMVar_hsa_circ_228538,RMVar_hsa_circ_356721,RMVar_hsa_circ_369134,RMVar_hsa_circ_228546,RMVar_hsa_circ_321824,RMVar_hsa_circ_228549,RMVar_hsa_circ_307927,RMVar_hsa_circ_326565,RMVar_hsa_circ_228547,RMVar_hsa_circ_308891,RMVar_hsa_circ_68990,RMVar_hsa_circ_305903,RMVar_hsa_circ_228550,RMVar_hsa_circ_228551,RMVar_hsa_circ_228548 19256 RMVar_ID_19256 Human_SNP_ID_202950132 A-to-I Human chr4 + 128011333 128011333 128011333 ACCTCGCCCAGCTAATTTTTTGTATTTTTAGTAGTGATGGGGTTTCACCATGTTAGCCAGGATGG ACCTCGCCCAGCTAATTTTTTGTATTTTTAGTGGTGATGGGGTTTCACCATGTTAGCCAGGATGG A G ABHD18 Ensembl:ENSG00000164074 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1323076201 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6941,RMVar_hsa_circ_279023,RMVar_hsa_circ_288390,RMVar_hsa_circ_337031,RMVar_hsa_circ_300769,RMVar_hsa_circ_287896,RMVar_hsa_circ_38832,RMVar_hsa_circ_228537,RMVar_hsa_circ_228539,RMVar_hsa_circ_228540,RMVar_hsa_circ_228538,RMVar_hsa_circ_356721,RMVar_hsa_circ_369134,RMVar_hsa_circ_228546,RMVar_hsa_circ_321824,RMVar_hsa_circ_228549,RMVar_hsa_circ_307927,RMVar_hsa_circ_326565,RMVar_hsa_circ_228547,RMVar_hsa_circ_308891,RMVar_hsa_circ_68990,RMVar_hsa_circ_305903,RMVar_hsa_circ_228550,RMVar_hsa_circ_228551,RMVar_hsa_circ_228548 19257 RMVar_ID_19257 Human_SNP_ID_202950347 A-to-I Human chr4 + 128011999 128011999 128011999 AAATGATAAAACCCTTTCTTTTTTTTTTTTTGAGACGCAGTCATTCTGTCACCCAGTCTGGAGTG AAATGATAAAACCCTTTCTTTTTTTTTTTTTGTGACGCAGTCATTCTGTCACCCAGTCTGGAGTG A T ABHD18 Ensembl:ENSG00000164074 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1207397724 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15042986 RMVar_hsa_circ_6941,RMVar_hsa_circ_279023,RMVar_hsa_circ_288390,RMVar_hsa_circ_300769,RMVar_hsa_circ_287896,RMVar_hsa_circ_38832,RMVar_hsa_circ_228537,RMVar_hsa_circ_228539,RMVar_hsa_circ_228540,RMVar_hsa_circ_228538,RMVar_hsa_circ_369134,RMVar_hsa_circ_228546,RMVar_hsa_circ_321824,RMVar_hsa_circ_228549,RMVar_hsa_circ_307927,RMVar_hsa_circ_326565,RMVar_hsa_circ_228547,RMVar_hsa_circ_68990,RMVar_hsa_circ_305903,RMVar_hsa_circ_228550,RMVar_hsa_circ_228551,RMVar_hsa_circ_228548 19258 RMVar_ID_19258 Human_SNP_ID_202950512 A-to-I Human chr4 + 128012794 128012786 128012795 TGAGGTCAGAAAGATAGGCAAGGGCTGGCTGCAGTGGCTCACACATGTAATCCCAGCACTTTGGG TGAGGTCAGAAAGATAGGCAAGGGC_________TGGCTCACACATGTAATCCCAGCACTTTGGG CTGGCTGCAG C ABHD18 Ensembl:ENSG00000164074 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1379405556 Functional Loss DEL dbSNP153 26..34 33 - - - RMVar_hsa_circ_6941,RMVar_hsa_circ_279023,RMVar_hsa_circ_288390,RMVar_hsa_circ_300769,RMVar_hsa_circ_287896,RMVar_hsa_circ_38832,RMVar_hsa_circ_228537,RMVar_hsa_circ_228539,RMVar_hsa_circ_228540,RMVar_hsa_circ_228538,RMVar_hsa_circ_369134,RMVar_hsa_circ_228546,RMVar_hsa_circ_321824,RMVar_hsa_circ_228549,RMVar_hsa_circ_307927,RMVar_hsa_circ_326565,RMVar_hsa_circ_228547,RMVar_hsa_circ_68990,RMVar_hsa_circ_305903,RMVar_hsa_circ_228550,RMVar_hsa_circ_228551,RMVar_hsa_circ_228548 19259 RMVar_ID_19259 Human_SNP_ID_202950530 A-to-I Human chr4 + 128012865 128012865 128012865 AGGTGGGTGGATCACTTGGTGTCAGTAGTTCGAGACCAGCCTGACCAACATGGTAAAACCCTGTG AGGTGGGTGGATCACTTGGTGTCAGTAGTTCGTGACCAGCCTGACCAACATGGTAAAACCCTGTG A T ABHD18 Ensembl:ENSG00000164074 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1272045689 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6941,RMVar_hsa_circ_279023,RMVar_hsa_circ_288390,RMVar_hsa_circ_300769,RMVar_hsa_circ_287896,RMVar_hsa_circ_38832,RMVar_hsa_circ_228537,RMVar_hsa_circ_228539,RMVar_hsa_circ_228540,RMVar_hsa_circ_228538,RMVar_hsa_circ_369134,RMVar_hsa_circ_228546,RMVar_hsa_circ_321824,RMVar_hsa_circ_228549,RMVar_hsa_circ_307927,RMVar_hsa_circ_326565,RMVar_hsa_circ_228547,RMVar_hsa_circ_68990,RMVar_hsa_circ_305903,RMVar_hsa_circ_228550,RMVar_hsa_circ_228551,RMVar_hsa_circ_228548 19260 RMVar_ID_19260 Human_SNP_ID_202950550 A-to-I Human chr4 + 128012955 128012955 128012955 AGGCATGGTGGTATGCACCTGTAGTCCCAACTACTGGGGAGGCCGAGGCAGGAGAATCGCTTGAA AGGCATGGTGGTATGCACCTGTAGTCCCAACTGCTGGGGAGGCCGAGGCAGGAGAATCGCTTGAA A G ABHD18 Ensembl:ENSG00000164074 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1269590285 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6941,RMVar_hsa_circ_279023,RMVar_hsa_circ_288390,RMVar_hsa_circ_300769,RMVar_hsa_circ_287896,RMVar_hsa_circ_38832,RMVar_hsa_circ_228537,RMVar_hsa_circ_228539,RMVar_hsa_circ_228540,RMVar_hsa_circ_228538,RMVar_hsa_circ_369134,RMVar_hsa_circ_228546,RMVar_hsa_circ_321824,RMVar_hsa_circ_228549,RMVar_hsa_circ_307927,RMVar_hsa_circ_326565,RMVar_hsa_circ_228547,RMVar_hsa_circ_68990,RMVar_hsa_circ_305903,RMVar_hsa_circ_228550,RMVar_hsa_circ_228551,RMVar_hsa_circ_228548 19261 RMVar_ID_19261 Human_SNP_ID_202950836 A-to-I Human chr4 + 128014083 128014083 128014083 TCTGCTCTCTGCAACCTCCGCCTTCTGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGC TCTGCTCTCTGCAACCTCCGCCTTCTGGGTTCGAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGC A G ABHD18 Ensembl:ENSG00000164074 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs961939855 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6941,RMVar_hsa_circ_279023,RMVar_hsa_circ_288390,RMVar_hsa_circ_300769,RMVar_hsa_circ_287896,RMVar_hsa_circ_38832,RMVar_hsa_circ_228537,RMVar_hsa_circ_228539,RMVar_hsa_circ_228540,RMVar_hsa_circ_228538,RMVar_hsa_circ_369134,RMVar_hsa_circ_228546,RMVar_hsa_circ_321824,RMVar_hsa_circ_228549,RMVar_hsa_circ_307927,RMVar_hsa_circ_326565,RMVar_hsa_circ_228547,RMVar_hsa_circ_68990,RMVar_hsa_circ_305903,RMVar_hsa_circ_228550,RMVar_hsa_circ_228551,RMVar_hsa_circ_228548 19262 RMVar_ID_19262 Human_SNP_ID_202951069 A-to-I Human chr4 + 128015002 128015002 128015002 AGGATGCTGAGGCAGGAGAATCGCTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCCAAGATCGCC AGGATGCTGAGGCAGGAGAATCGCTTGAACCCCGGAGGCAGAGGTTGCAGTGAGCCAAGATCGCC A C ABHD18 Ensembl:ENSG00000164074 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1420580010 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6941,RMVar_hsa_circ_279023,RMVar_hsa_circ_288390,RMVar_hsa_circ_300769,RMVar_hsa_circ_287896,RMVar_hsa_circ_38832,RMVar_hsa_circ_228537,RMVar_hsa_circ_228539,RMVar_hsa_circ_228540,RMVar_hsa_circ_228538,RMVar_hsa_circ_369134,RMVar_hsa_circ_228546,RMVar_hsa_circ_321824,RMVar_hsa_circ_228549,RMVar_hsa_circ_307927,RMVar_hsa_circ_326565,RMVar_hsa_circ_228547,RMVar_hsa_circ_68990,RMVar_hsa_circ_305903,RMVar_hsa_circ_228550,RMVar_hsa_circ_228551,RMVar_hsa_circ_228548 19263 RMVar_ID_19263 Human_SNP_ID_202951354 A-to-I Human chr4 + 128016156 128016156 128016156 TTGTATTTTTAGTAGAGACAGGGTTTTATCCTATTGGTCAGGCTGGTCTCTAACTCCTGACCTCA TTGTATTTTTAGTAGAGACAGGGTTTTATCCTGTTGGTCAGGCTGGTCTCTAACTCCTGACCTCA A G ABHD18 Ensembl:ENSG00000164074 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1307563209 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_163061 RMVar_hsa_circ_6941,RMVar_hsa_circ_279023,RMVar_hsa_circ_288390,RMVar_hsa_circ_300769,RMVar_hsa_circ_287896,RMVar_hsa_circ_38832,RMVar_hsa_circ_228537,RMVar_hsa_circ_228539,RMVar_hsa_circ_228540,RMVar_hsa_circ_228538,RMVar_hsa_circ_369134,RMVar_hsa_circ_228546,RMVar_hsa_circ_321824,RMVar_hsa_circ_228549,RMVar_hsa_circ_307927,RMVar_hsa_circ_326565,RMVar_hsa_circ_228547,RMVar_hsa_circ_68990,RMVar_hsa_circ_305903,RMVar_hsa_circ_228550,RMVar_hsa_circ_228551,RMVar_hsa_circ_228548 19264 RMVar_ID_19264 Human_SNP_ID_202951541 A-to-I Human chr4 + 128016941 128016940 128016942 GTAATTCTATTTTTTTTTTCTCTTTTTGAGACAGGGTCTCATTCTGTTGCCCAGGCTGGAGTACA GTAATTCTATTTTTTTTTTCTCTTTTTGAGAC__GGTCTCATTCTGTTGCCCAGGCTGGAGTACA CAG C ABHD18 Ensembl:ENSG00000164074 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1487009719 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_6941,RMVar_hsa_circ_279023,RMVar_hsa_circ_288390,RMVar_hsa_circ_300769,RMVar_hsa_circ_287896,RMVar_hsa_circ_38832,RMVar_hsa_circ_228537,RMVar_hsa_circ_228539,RMVar_hsa_circ_228540,RMVar_hsa_circ_228538,RMVar_hsa_circ_369134,RMVar_hsa_circ_228546,RMVar_hsa_circ_321824,RMVar_hsa_circ_228549,RMVar_hsa_circ_307927,RMVar_hsa_circ_326565,RMVar_hsa_circ_228547,RMVar_hsa_circ_68990,RMVar_hsa_circ_305903,RMVar_hsa_circ_228550,RMVar_hsa_circ_228551,RMVar_hsa_circ_228548 19265 RMVar_ID_19265 Human_SNP_ID_202951554 A-to-I Human chr4 + 128017017 128017017 128017017 TCAGCTCACTGCAGCCTCTGCCTCCCAGGTTCAAGCGATTTTCATGCCTCAGTTTTCCACGTAGC TCAGCTCACTGCAGCCTCTGCCTCCCAGGTTCGAGCGATTTTCATGCCTCAGTTTTCCACGTAGC A G ABHD18 Ensembl:ENSG00000164074 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs746218280 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6941,RMVar_hsa_circ_279023,RMVar_hsa_circ_288390,RMVar_hsa_circ_300769,RMVar_hsa_circ_287896,RMVar_hsa_circ_38832,RMVar_hsa_circ_228537,RMVar_hsa_circ_228539,RMVar_hsa_circ_228540,RMVar_hsa_circ_228538,RMVar_hsa_circ_369134,RMVar_hsa_circ_228546,RMVar_hsa_circ_321824,RMVar_hsa_circ_228549,RMVar_hsa_circ_307927,RMVar_hsa_circ_326565,RMVar_hsa_circ_228547,RMVar_hsa_circ_68990,RMVar_hsa_circ_305903,RMVar_hsa_circ_228550,RMVar_hsa_circ_228551,RMVar_hsa_circ_228548 19266 RMVar_ID_19266 Human_SNP_ID_202955252 A-to-I Human chr4 + 128032475 128032475 128032475 TCAGGAGGCCAAGGCGGGTGGATCATGACATCAGGAGTTCGAGCCCAGCCTGGCCAATATGGTAA TCAGGAGGCCAAGGCGGGTGGATCATGACATCCGGAGTTCGAGCCCAGCCTGGCCAATATGGTAA A C ABHD18 Ensembl:ENSG00000164074 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs925088031 Functional Loss SNV dbSNP153 33..33 33 - - - 19267 RMVar_ID_19267 Human_SNP_ID_202955259 A-to-I Human chr4 + 128032506 128032506 128032506 CAGGAGTTCGAGCCCAGCCTGGCCAATATGGTAAAACCCCGTCTCTACTAAAAATACAAAAATTA CAGGAGTTCGAGCCCAGCCTGGCCAATATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTA A G ABHD18 Ensembl:ENSG00000164074 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs949035334 Functional Loss SNV dbSNP153 33..33 33 - - - 19268 RMVar_ID_19268 Human_SNP_ID_202955760 A-to-I Human chr4 + 128034239 128034239 128034239 TTGGCCTTCCAAAGTGCTGGGATTACAGGCGTAAGCCACCGCGCCTGGCCTAGACATGCATTTTC TTGGCCTTCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCCTGGCCTAGACATGCATTTTC A G ABHD18 Ensembl:ENSG00000164074 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs558953045 Functional Loss SNV dbSNP153 33..33 33 - - - 19269 RMVar_ID_19269 Human_SNP_ID_202955896 A-to-I Human chr4 + 128034780 128034780 128034780 TCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTATAGGCATGTGCCACCACACCCG TCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTGGCTGGGATTATAGGCATGTGCCACCACACCCG A G ABHD18 Ensembl:ENSG00000164074 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1283982012 Functional Loss SNV dbSNP153 33..33 33 - - - 19270 RMVar_ID_19270 Human_SNP_ID_202955910 A-to-I Human chr4 + 128034826 128034825 128034826 GCATGTGCCACCACACCCGGCTAATTTTTTGTAATTTTAGTAGAGACGGGGTTTCTCCATGTTGA GCATGTGCCACCACACCCGGCTAATTTTTTGT_ATTTTAGTAGAGACGGGGTTTCTCCATGTTGA TA T ABHD18 Ensembl:ENSG00000164074 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs769865633 Functional Loss DEL dbSNP153 33..33 33 - - - 19271 RMVar_ID_19271 Human_SNP_ID_202955912 A-to-I Human chr4 + 128034832 128034832 128034832 GCCACCACACCCGGCTAATTTTTTGTAATTTTAGTAGAGACGGGGTTTCTCCATGTTGATCAGGC GCCACCACACCCGGCTAATTTTTTGTAATTTTTGTAGAGACGGGGTTTCTCCATGTTGATCAGGC A T ABHD18 Ensembl:ENSG00000164074 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs919223851 Functional Loss SNV dbSNP153 33..33 33 - - - 19272 RMVar_ID_19272 Human_SNP_ID_202956316 A-to-I Human chr4 + 128036609 128036609 128036609 AAAAAATTAGCCAAGCATGGTGGCGCATGCCTATAATCCCAGATACTCAGGAGGCAGAGGCAGGA AAAAAATTAGCCAAGCATGGTGGCGCATGCCTGTAATCCCAGATACTCAGGAGGCAGAGGCAGGA A G ABHD18 Ensembl:ENSG00000164074 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs1263217351 Functional Loss SNV dbSNP153 33..33 33 - - - 19273 RMVar_ID_19273 Human_SNP_ID_202956552 A-to-I Human chr4 + 128037402 128037402 128037402 ACCTGTTGCATTAACTGACGGAGTGCAGTGGCATGATCTTGGCTCACTGCGACCTCCGCCTCTCA ACCTGTTGCATTAACTGACGGAGTGCAGTGGCGTGATCTTGGCTCACTGCGACCTCCGCCTCTCA A G ABHD18 Ensembl:ENSG00000164074 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1044271677 Functional Loss SNV dbSNP153 33..33 33 - - - 19274 RMVar_ID_19274 Human_SNP_ID_202956565 A-to-I Human chr4 + 128037434 128037434 128037434 ATGATCTTGGCTCACTGCGACCTCCGCCTCTCAGGTTCAAGCGGTTCTCCTGCCTCCACCTGAGT ATGATCTTGGCTCACTGCGACCTCCGCCTCTCGGGTTCAAGCGGTTCTCCTGCCTCCACCTGAGT A G ABHD18 Ensembl:ENSG00000164074 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1463215311 Functional Loss SNV dbSNP153 33..33 33 - - - 19275 RMVar_ID_19275 Human_SNP_ID_202956623 A-to-I Human chr4 + 128037612 128037612 128037612 TGCCTGCCTTGGCCTCCCAAAGTGCTGGGATTATAGGTTTGAGCCACCACACCCGACCTGACATT TGCCTGCCTTGGCCTCCCAAAGTGCTGGGATTGTAGGTTTGAGCCACCACACCCGACCTGACATT A G ABHD18 Ensembl:ENSG00000164074 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs908619464 Functional Loss SNV dbSNP153 33..33 33 - - - 19276 RMVar_ID_19276 Human_SNP_ID_202956883 A-to-I Human chr4 + 128038767 128038767 128038767 ACAAAATTTTTAAAAAAAATACAAAATTAGCCAGGCGTGGTGGCACATGCCTGTAATCCCAGCTA ACAAAATTTTTAAAAAAAATACAAAATTAGCCGGGCGTGGTGGCACATGCCTGTAATCCCAGCTA A G ABHD18 Ensembl:ENSG00000164074 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs997781139 Functional Loss SNV dbSNP153 33..33 33 - - - 19277 RMVar_ID_19277 Human_SNP_ID_202965930 A-to-I Human chr4 + 128068665 128068665 128068665 ATTCTTGGCGGCCTCAAAGGATTCCCTGCCTCAGCCTCCCAAAGTGCTGCTATTACAGGTGTGAG ATTCTTGGCGGCCTCAAAGGATTCCCTGCCTCCGCCTCCCAAAGTGCTGCTATTACAGGTGTGAG A C LARP1B Ensembl:ENSG00000138709 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs979318056 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_228558,RMVar_hsa_circ_102311 19278 RMVar_ID_19278 Human_SNP_ID_202969343 A-to-I Human chr4 + 128081127 128081127 128081127 TGAGACAGACTCTCGTCTCTGTCACCCAGGCTAGAGTGCAGTGGCACGATCTCGGCTCACTGCAA TGAGACAGACTCTCGTCTCTGTCACCCAGGCTGGAGTGCAGTGGCACGATCTCGGCTCACTGCAA A G LARP1B Ensembl:ENSG00000138709 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991560227 Functional Loss SNV dbSNP153 33..33 33 - - - 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_277689,RMVar_hsa_circ_64803,RMVar_hsa_circ_228565,RMVar_hsa_circ_228567,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_228570,RMVar_hsa_circ_358732,RMVar_hsa_circ_372310,RMVar_hsa_circ_349074,RMVar_hsa_circ_62080,RMVar_hsa_circ_272205,RMVar_hsa_circ_228571 19279 RMVar_ID_19279 Human_SNP_ID_202973487 A-to-I Human chr4 + 128094568 128094568 128094568 AGCTGGGATTAGAGGCACGTGACACTGCGCCCAGCTAATTTTTGTATTTTTAGTAGAGACAGGGT AGCTGGGATTAGAGGCACGTGACACTGCGCCCGGCTAATTTTTGTATTTTTAGTAGAGACAGGGT A G LARP1B Ensembl:ENSG00000138709 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1039881110 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9150,RMVar_hsa_circ_228561,RMVar_hsa_circ_292877,RMVar_hsa_circ_329939,RMVar_hsa_circ_360511,RMVar_hsa_circ_281172,RMVar_hsa_circ_14883,RMVar_hsa_circ_94553,RMVar_hsa_circ_64803,RMVar_hsa_circ_228563,RMVar_hsa_circ_228562,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_56376,RMVar_hsa_circ_228575,RMVar_hsa_circ_298169,RMVar_hsa_circ_367230,RMVar_hsa_circ_349277,RMVar_hsa_circ_334772,RMVar_hsa_circ_30153,RMVar_hsa_circ_79919,RMVar_hsa_circ_228573,RMVar_hsa_circ_228574,RMVar_hsa_circ_64315 19280 RMVar_ID_19280 Human_SNP_ID_202973497 A-to-I Human chr4 + 128094607 128094607 128094607 TTTTGTATTTTTAGTAGAGACAGGGTTTTGCCATGTTGCCCCATCTGGTCTCGAATGCCTGAGCT TTTTGTATTTTTAGTAGAGACAGGGTTTTGCCCTGTTGCCCCATCTGGTCTCGAATGCCTGAGCT A C LARP1B Ensembl:ENSG00000138709 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270113216 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9150,RMVar_hsa_circ_228561,RMVar_hsa_circ_292877,RMVar_hsa_circ_329939,RMVar_hsa_circ_360511,RMVar_hsa_circ_281172,RMVar_hsa_circ_14883,RMVar_hsa_circ_94553,RMVar_hsa_circ_64803,RMVar_hsa_circ_228563,RMVar_hsa_circ_228562,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_56376,RMVar_hsa_circ_228575,RMVar_hsa_circ_298169,RMVar_hsa_circ_367230,RMVar_hsa_circ_349277,RMVar_hsa_circ_334772,RMVar_hsa_circ_30153,RMVar_hsa_circ_79919,RMVar_hsa_circ_228573,RMVar_hsa_circ_228574,RMVar_hsa_circ_64315 19281 RMVar_ID_19281 Human_SNP_ID_202973498 A-to-I Human chr4 + 128094607 128094607 128094607 TTTTGTATTTTTAGTAGAGACAGGGTTTTGCCATGTTGCCCCATCTGGTCTCGAATGCCTGAGCT TTTTGTATTTTTAGTAGAGACAGGGTTTTGCCGTGTTGCCCCATCTGGTCTCGAATGCCTGAGCT A G LARP1B Ensembl:ENSG00000138709 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270113216 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9150,RMVar_hsa_circ_228561,RMVar_hsa_circ_292877,RMVar_hsa_circ_329939,RMVar_hsa_circ_360511,RMVar_hsa_circ_281172,RMVar_hsa_circ_14883,RMVar_hsa_circ_94553,RMVar_hsa_circ_64803,RMVar_hsa_circ_228563,RMVar_hsa_circ_228562,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_56376,RMVar_hsa_circ_228575,RMVar_hsa_circ_298169,RMVar_hsa_circ_367230,RMVar_hsa_circ_349277,RMVar_hsa_circ_334772,RMVar_hsa_circ_30153,RMVar_hsa_circ_79919,RMVar_hsa_circ_228573,RMVar_hsa_circ_228574,RMVar_hsa_circ_64315 19282 RMVar_ID_19282 Human_SNP_ID_202975046 A-to-I Human chr4 + 128099044 128099044 128099044 GTGATCCGCCCACCTTCGCCTCCCAAAATGCTAGGATTACAGGTGTGAGCCAGCACTCCCAGCCG GTGATCCGCCCACCTTCGCCTCCCAAAATGCTGGGATTACAGGTGTGAGCCAGCACTCCCAGCCG A G LARP1B Ensembl:ENSG00000138709 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs915236164 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9150,RMVar_hsa_circ_228561,RMVar_hsa_circ_292877,RMVar_hsa_circ_329939,RMVar_hsa_circ_360511,RMVar_hsa_circ_14883,RMVar_hsa_circ_94553,RMVar_hsa_circ_64803,RMVar_hsa_circ_228562,RMVar_hsa_circ_228559,RMVar_hsa_circ_228560,RMVar_hsa_circ_358732,RMVar_hsa_circ_62080,RMVar_hsa_circ_360384,RMVar_hsa_circ_330140,RMVar_hsa_circ_18140,RMVar_hsa_circ_56376,RMVar_hsa_circ_228575,RMVar_hsa_circ_298169,RMVar_hsa_circ_367230,RMVar_hsa_circ_349277,RMVar_hsa_circ_30153,RMVar_hsa_circ_79919,RMVar_hsa_circ_228573,RMVar_hsa_circ_228574,RMVar_hsa_circ_64315,RMVar_hsa_circ_32801,RMVar_hsa_circ_286250,RMVar_hsa_circ_347506,RMVar_hsa_circ_55986,RMVar_hsa_circ_228579,RMVar_hsa_circ_16546,RMVar_hsa_circ_228578 19283 RMVar_ID_19283 Human_SNP_ID_202978491 A-to-I Human chr4 + 128111596 128111596 128111596 GTGGTGGTGTGCATGTGTAGTACTAGTTATTCAGCAGGCTGAGTTGAGAGGATTACTTGAGCGCA GTGGTGGTGTGCATGTGTAGTACTAGTTATTCTGCAGGCTGAGTTGAGAGGATTACTTGAGCGCA A T LARP1B Ensembl:ENSG00000138709 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1173984408 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15043669 RMVar_hsa_circ_9150,RMVar_hsa_circ_228561,RMVar_hsa_circ_292877,RMVar_hsa_circ_329939,RMVar_hsa_circ_14883,RMVar_hsa_circ_94553,RMVar_hsa_circ_64803,RMVar_hsa_circ_228559,RMVar_hsa_circ_228560,RMVar_hsa_circ_358732,RMVar_hsa_circ_62080,RMVar_hsa_circ_360384,RMVar_hsa_circ_330140,RMVar_hsa_circ_18140,RMVar_hsa_circ_73847,RMVar_hsa_circ_56376,RMVar_hsa_circ_228575,RMVar_hsa_circ_298169,RMVar_hsa_circ_367230,RMVar_hsa_circ_349277,RMVar_hsa_circ_30153,RMVar_hsa_circ_79919,RMVar_hsa_circ_228573,RMVar_hsa_circ_228574,RMVar_hsa_circ_32801,RMVar_hsa_circ_286250,RMVar_hsa_circ_347506,RMVar_hsa_circ_55986,RMVar_hsa_circ_228579,RMVar_hsa_circ_228578,RMVar_hsa_circ_363607 19284 RMVar_ID_19284 Human_SNP_ID_202979430 A-to-I Human chr4 + 128115031 128115031 128115031 GCGATCTTGGCTCACTGCCACCTCTGCCTCCCAGGTTCAAGCGATTCTCCTGCCCTGGCCTCCTG GCGATCTTGGCTCACTGCCACCTCTGCCTCCCGGGTTCAAGCGATTCTCCTGCCCTGGCCTCCTG A G LARP1B Ensembl:ENSG00000138709 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1230151068 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9150,RMVar_hsa_circ_329939,RMVar_hsa_circ_14883,RMVar_hsa_circ_94553,RMVar_hsa_circ_64803,RMVar_hsa_circ_228559,RMVar_hsa_circ_228560,RMVar_hsa_circ_358732,RMVar_hsa_circ_62080,RMVar_hsa_circ_360384,RMVar_hsa_circ_330140,RMVar_hsa_circ_18140,RMVar_hsa_circ_73847,RMVar_hsa_circ_298169,RMVar_hsa_circ_367230,RMVar_hsa_circ_30153,RMVar_hsa_circ_79919,RMVar_hsa_circ_228573,RMVar_hsa_circ_228574,RMVar_hsa_circ_32801,RMVar_hsa_circ_286250,RMVar_hsa_circ_347506,RMVar_hsa_circ_228579,RMVar_hsa_circ_228578,RMVar_hsa_circ_363607,RMVar_hsa_circ_228580,RMVar_hsa_circ_274369,RMVar_hsa_circ_301668,RMVar_hsa_circ_318172,RMVar_hsa_circ_344139,RMVar_hsa_circ_345249,RMVar_hsa_circ_342227,RMVar_hsa_circ_305618,RMVar_hsa_circ_291163,RMVar_hsa_circ_228582,RMVar_hsa_circ_228583,RMVar_hsa_circ_228581 19285 RMVar_ID_19285 Human_SNP_ID_202984095 A-to-I Human chr4 + 128133836 128133836 128133836 CTCCTGCCTCAGCCTCTCGAGTAGCTGGGACTACAGGCCTGCACCACCATGCCCGACCATTGTTT CTCCTGCCTCAGCCTCTCGAGTAGCTGGGACTGCAGGCCTGCACCACCATGCCCGACCATTGTTT A G LARP1B Ensembl:ENSG00000138709 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs779519049 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9150,RMVar_hsa_circ_14883,RMVar_hsa_circ_94553,RMVar_hsa_circ_64803,RMVar_hsa_circ_228559,RMVar_hsa_circ_360384,RMVar_hsa_circ_330140,RMVar_hsa_circ_367230,RMVar_hsa_circ_30153,RMVar_hsa_circ_79919,RMVar_hsa_circ_228573,RMVar_hsa_circ_32801,RMVar_hsa_circ_347506,RMVar_hsa_circ_228579,RMVar_hsa_circ_228578,RMVar_hsa_circ_363607,RMVar_hsa_circ_228580,RMVar_hsa_circ_274369,RMVar_hsa_circ_301668,RMVar_hsa_circ_318172,RMVar_hsa_circ_345249,RMVar_hsa_circ_342227,RMVar_hsa_circ_305618,RMVar_hsa_circ_291163,RMVar_hsa_circ_228582,RMVar_hsa_circ_228583,RMVar_hsa_circ_228581,RMVar_hsa_circ_299442,RMVar_hsa_circ_311096,RMVar_hsa_circ_320128,RMVar_hsa_circ_308865,RMVar_hsa_circ_294981,RMVar_hsa_circ_282605,RMVar_hsa_circ_228586,RMVar_hsa_circ_228588,RMVar_hsa_circ_228589,RMVar_hsa_circ_228587,RMVar_hsa_circ_228584,RMVar_hsa_circ_228585 19286 RMVar_ID_19286 Human_SNP_ID_202984200 A-to-I Human chr4 + 128134261 128134261 128134261 GGCCTTAAGCAATCCTTCCATCTTGGCCTTGCAAAGTATTGGGATTACAGGTGTGAGCTACTGAA GGCCTTAAGCAATCCTTCCATCTTGGCCTTGCCAAGTATTGGGATTACAGGTGTGAGCTACTGAA A C LARP1B Ensembl:ENSG00000138709 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913748446 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9150,RMVar_hsa_circ_14883,RMVar_hsa_circ_94553,RMVar_hsa_circ_64803,RMVar_hsa_circ_228559,RMVar_hsa_circ_360384,RMVar_hsa_circ_330140,RMVar_hsa_circ_367230,RMVar_hsa_circ_30153,RMVar_hsa_circ_79919,RMVar_hsa_circ_228573,RMVar_hsa_circ_32801,RMVar_hsa_circ_347506,RMVar_hsa_circ_228579,RMVar_hsa_circ_228578,RMVar_hsa_circ_363607,RMVar_hsa_circ_228580,RMVar_hsa_circ_274369,RMVar_hsa_circ_301668,RMVar_hsa_circ_318172,RMVar_hsa_circ_345249,RMVar_hsa_circ_342227,RMVar_hsa_circ_305618,RMVar_hsa_circ_291163,RMVar_hsa_circ_228582,RMVar_hsa_circ_228583,RMVar_hsa_circ_228581,RMVar_hsa_circ_299442,RMVar_hsa_circ_311096,RMVar_hsa_circ_320128,RMVar_hsa_circ_308865,RMVar_hsa_circ_294981,RMVar_hsa_circ_282605,RMVar_hsa_circ_228586,RMVar_hsa_circ_228588,RMVar_hsa_circ_228589,RMVar_hsa_circ_228587,RMVar_hsa_circ_228584,RMVar_hsa_circ_228585 19287 RMVar_ID_19287 Human_SNP_ID_202988038 A-to-I Human chr4 + 128150343 128150343 128150343 GACAGGGTCTCACCCTGTTGTGCCTAGGCTGGAATGCAGTGGTGAGATCATAGCGTACTGCAGCC GACAGGGTCTCACCCTGTTGTGCCTAGGCTGGGATGCAGTGGTGAGATCATAGCGTACTGCAGCC A G LARP1B Ensembl:ENSG00000138709 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1375265738 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9150,RMVar_hsa_circ_14883,RMVar_hsa_circ_94553,RMVar_hsa_circ_64803,RMVar_hsa_circ_228559,RMVar_hsa_circ_360384,RMVar_hsa_circ_330140,RMVar_hsa_circ_367230,RMVar_hsa_circ_30153,RMVar_hsa_circ_79919,RMVar_hsa_circ_228573,RMVar_hsa_circ_32801,RMVar_hsa_circ_347506,RMVar_hsa_circ_228579,RMVar_hsa_circ_228578,RMVar_hsa_circ_363607,RMVar_hsa_circ_228580,RMVar_hsa_circ_274369,RMVar_hsa_circ_301668,RMVar_hsa_circ_318172,RMVar_hsa_circ_345249,RMVar_hsa_circ_342227,RMVar_hsa_circ_305618,RMVar_hsa_circ_291163,RMVar_hsa_circ_228582,RMVar_hsa_circ_228583,RMVar_hsa_circ_228581,RMVar_hsa_circ_299442,RMVar_hsa_circ_311096,RMVar_hsa_circ_320128,RMVar_hsa_circ_308865,RMVar_hsa_circ_294981,RMVar_hsa_circ_282605,RMVar_hsa_circ_228586,RMVar_hsa_circ_228588,RMVar_hsa_circ_228589,RMVar_hsa_circ_228587,RMVar_hsa_circ_228584,RMVar_hsa_circ_228585 19288 RMVar_ID_19288 Human_SNP_ID_202989376 A-to-I Human chr4 - 128155778 128155778 128155778 TCCAGTTTATCAGTCTCCGCCTGCAGGAAGTCAGTCAGTTCCTTCCTCCAGTTCCTACACTTGGC TCCAGTTTATCAGTCTCCGCCTGCAGGAAGTCTGTCAGTTCCTTCCTCCAGTTCCTACACTTGGC T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1010877202 Functional Loss SNV dbSNP153 33..33 33 - - - 19289 RMVar_ID_19289 Human_SNP_ID_202989383 A-to-I Human chr4 - 128155802 128155802 128155802 CGCTGCAGCCCTGATTTCTCATCTTCCAGTTTATCAGTCTCCGCCTGCAGGAAGTCAGTCAGTTC CGCTGCAGCCCTGATTTCTCATCTTCCAGTTTGTCAGTCTCCGCCTGCAGGAAGTCAGTCAGTTC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1394331066 Functional Loss SNV dbSNP153 33..33 33 - - - 19290 RMVar_ID_19290 Human_SNP_ID_203015701 A-to-I Human chr4 - 128269904 128269904 128269904 ATTATTCAGGTAAGAATTGGTATATTAAATGTACATCTTTTTACTTTCTATTTTGATGCCAACTG ATTATTCAGGTAAGAATTGGTATATTAAATGTGCATCTTTTTACTTTCTATTTTGATGCCAACTG T C PGRMC2 Ensembl:ENSG00000164040 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs563412381 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7347683,Human_RBP_ID_18018164,Human_RBP_ID_26689533 Human_miRNA_ID_1427997 19291 RMVar_ID_19291 Human_SNP_ID_203063162 A-to-I Human chr4 + 128478202 128478202 128478202 CAATAGACCTCCAGAACTTATTCCTTCTGTATAACTGATACTTTGTACCCTTTGACTGGCAGCTC CAATAGACCTCCAGAACTTATTCCTTCTGTATGACTGATACTTTGTACCCTTTGACTGGCAGCTC A G LINC02615 Ensembl:ENSG00000251432 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1019287851 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_359762,RMVar_hsa_circ_47470 19292 RMVar_ID_19292 Human_SNP_ID_203067770 A-to-I Human chr4 + 128499616 128499616 128499616 CTAGGGAGACCTCAGGAATACAATCATGGCAGAAGGTGAAGGAGAAGCAAGGCACATCTTACATG CTAGGGAGACCTCAGGAATACAATCATGGCAGGAGGTGAAGGAGAAGCAAGGCACATCTTACATG A G LINC02615 Ensembl:ENSG00000251432 lincRNA intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs930394373 Functional Loss SNV dbSNP153 33..33 33 - - - 19293 RMVar_ID_19293 Human_SNP_ID_203068354 A-to-I Human chr4 + 128502186 128502186 128502186 CACCCCTAGATTCTATTGTGGGGCCGGAGCCCAAAAGTGCTCACACCAGCTTCTGCACCTGCCCA CACCCCTAGATTCTATTGTGGGGCCGGAGCCCCAAAGTGCTCACACCAGCTTCTGCACCTGCCCA A C LINC02615 Ensembl:ENSG00000251432 lincRNA intron GSE100210;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229 RNA-Seq:(High) rs1469135355 Functional Loss SNV dbSNP153 33..33 33 - - - 19294 RMVar_ID_19294 Human_SNP_ID_203068843 A-to-I Human chr4 + 128504654 128504654 128504654 AGTTGCATGAACGAATTGAGGATGCTAAATGCAGGGGATTTTGTTGCCGATGAAAGTGGCTCTCA AGTTGCATGAACGAATTGAGGATGCTAAATGCGGGGGATTTTGTTGCCGATGAAAGTGGCTCTCA A G LINC02615 Ensembl:ENSG00000251432 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1393645787 Functional Loss SNV dbSNP153 33..33 33 - - - 19295 RMVar_ID_19295 Human_SNP_ID_203068850 A-to-I Human chr4 + 128504675 128504675 128504675 ATGCTAAATGCAGGGGATTTTGTTGCCGATGAAAGTGGCTCTCAGTATAATGGAGAGCTGGAAAG ATGCTAAATGCAGGGGATTTTGTTGCCGATGAGAGTGGCTCTCAGTATAATGGAGAGCTGGAAAG A G LINC02615 Ensembl:ENSG00000251432 lincRNA intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs188541978 Functional Loss SNV dbSNP153 33..33 33 - - - 19296 RMVar_ID_19296 Human_SNP_ID_203070167 A-to-I Human chr4 + 128510808 128510801 128510809 ACATGGCGAAACCCTGTCTCTTTACTAAAAATACAAAAAATTAGCCAGGCGTGGTAGTGGGTGCC ACATGGCGAAACCCTGTCTCTTTACT________AAAAAATTAGCCAGGCGTGGTAGTGGGTGCC TAAAAATAC T LINC02615 Ensembl:ENSG00000251432 lincRNA intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1374711989 Functional Loss DEL dbSNP153 27..34 33 - - - 19297 RMVar_ID_19297 Human_SNP_ID_203070171 A-to-I Human chr4 + 128510808 128510808 128510808 ACATGGCGAAACCCTGTCTCTTTACTAAAAATACAAAAAATTAGCCAGGCGTGGTAGTGGGTGCC ACATGGCGAAACCCTGTCTCTTTACTAAAAATGCAAAAAATTAGCCAGGCGTGGTAGTGGGTGCC A G LINC02615 Ensembl:ENSG00000251432 lincRNA intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs531311464 Functional Loss SNV dbSNP153 33..33 33 - - - 19298 RMVar_ID_19298 Human_SNP_ID_203080676 A-to-I Human chr4 + 128557334 128557334 128557334 GCTGGAGTACACTGGCACAATTATAACTCACTACAGCTTTGAACTCCTAGACTCAAGTAATCCTC GCTGGAGTACACTGGCACAATTATAACTCACTGCAGCTTTGAACTCCTAGACTCAAGTAATCCTC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1430421979 Functional Loss SNV dbSNP153 33..33 33 - - - 19299 RMVar_ID_19299 Human_SNP_ID_203180923 A-to-I Human chr4 - 128971915 128971915 128971915 AGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCACGCGTGCCATCA AGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCACGCGTGCCATCA T C SCLT1 Ensembl:ENSG00000151466 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1303709299 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57671,RMVar_hsa_circ_52846,RMVar_hsa_circ_48495,RMVar_hsa_circ_15978,RMVar_hsa_circ_337487,RMVar_hsa_circ_113174,RMVar_hsa_circ_116791,RMVar_hsa_circ_228613,RMVar_hsa_circ_228614,RMVar_hsa_circ_367290,RMVar_hsa_circ_304426,RMVar_hsa_circ_274096,RMVar_hsa_circ_228618,RMVar_hsa_circ_228619,RMVar_hsa_circ_55236,RMVar_hsa_circ_269186,RMVar_hsa_circ_283177,RMVar_hsa_circ_267083,RMVar_hsa_circ_228621,RMVar_hsa_circ_228622,RMVar_hsa_circ_267319,RMVar_hsa_circ_278953,RMVar_hsa_circ_304585,RMVar_hsa_circ_41681,RMVar_hsa_circ_228623,RMVar_hsa_circ_228624,RMVar_hsa_circ_359291,RMVar_hsa_circ_269042,RMVar_hsa_circ_367045,RMVar_hsa_circ_71790,RMVar_hsa_circ_228626,RMVar_hsa_circ_266662,RMVar_hsa_circ_297849,RMVar_hsa_circ_301075,RMVar_hsa_circ_367373,RMVar_hsa_circ_283458,RMVar_hsa_circ_228628,RMVar_hsa_circ_228629,RMVar_hsa_circ_228627 19300 RMVar_ID_19300 Human_SNP_ID_203181983 A-to-I Human chr4 - 128976580 128976580 128976580 AATTACATTGAGCTGAAAGTTTAAATTGGGTAAGGTAGATATGATCATCTATGAAGGAGAAAAAT AATTACATTGAGCTGAAAGTTTAAATTGGGTAGGGTAGATATGATCATCTATGAAGGAGAAAAAT T C SCLT1 Ensembl:ENSG00000151466 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs899792332 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20997644 RMVar_hsa_circ_57671,RMVar_hsa_circ_52846,RMVar_hsa_circ_48495,RMVar_hsa_circ_15978,RMVar_hsa_circ_337487,RMVar_hsa_circ_113174,RMVar_hsa_circ_116791,RMVar_hsa_circ_228613,RMVar_hsa_circ_228614,RMVar_hsa_circ_367290,RMVar_hsa_circ_304426,RMVar_hsa_circ_274096,RMVar_hsa_circ_228618,RMVar_hsa_circ_228619,RMVar_hsa_circ_55236,RMVar_hsa_circ_269186,RMVar_hsa_circ_283177,RMVar_hsa_circ_267083,RMVar_hsa_circ_228621,RMVar_hsa_circ_228622,RMVar_hsa_circ_267319,RMVar_hsa_circ_278953,RMVar_hsa_circ_304585,RMVar_hsa_circ_41681,RMVar_hsa_circ_228623,RMVar_hsa_circ_228624,RMVar_hsa_circ_359291,RMVar_hsa_circ_269042,RMVar_hsa_circ_367045,RMVar_hsa_circ_71790,RMVar_hsa_circ_228626,RMVar_hsa_circ_266662,RMVar_hsa_circ_297849,RMVar_hsa_circ_301075,RMVar_hsa_circ_367373,RMVar_hsa_circ_283458,RMVar_hsa_circ_228628,RMVar_hsa_circ_228629,RMVar_hsa_circ_228627 19301 RMVar_ID_19301 Human_SNP_ID_203198229 A-to-I Human chr4 - 129043187 129043187 129043187 TCTCTTCTAGCTGGGTGCGGTGGCTTATGCCTATAATCCCAGCACTTTGGGAGGCTGAGACAGGA TCTCTTCTAGCTGGGTGCGGTGGCTTATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGACAGGA T C SCLT1 Ensembl:ENSG00000151466 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1396550339 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15978,RMVar_hsa_circ_269186,RMVar_hsa_circ_228631,RMVar_hsa_circ_269042,RMVar_hsa_circ_71790,RMVar_hsa_circ_266662,RMVar_hsa_circ_331018,RMVar_hsa_circ_335744,RMVar_hsa_circ_20962,RMVar_hsa_circ_228635,RMVar_hsa_circ_372448,RMVar_hsa_circ_228630,RMVar_hsa_circ_331066,RMVar_hsa_circ_56524,RMVar_hsa_circ_337513,RMVar_hsa_circ_288849 19302 RMVar_ID_19302 Human_SNP_ID_204247974 A-to-I Human chr4 + 133183320 133183320 133183320 TGGTGAAACAGTTGTAAATGTACTGTTACCTTATGAGAAGGTAGTTTTGATTTACACATACACAT TGGTGAAACAGTTGTAAATGTACTGTTACCTTGTGAGAAGGTAGTTTTGATTTACACATACACAT A G PCDH10 Ensembl:ENSG00000138650 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs996194638 Functional Loss SNV dbSNP153 33..33 33 - - - 19303 RMVar_ID_19303 Human_SNP_ID_204247975 A-to-I Human chr4 + 133183320 133183320 133183320 TGGTGAAACAGTTGTAAATGTACTGTTACCTTATGAGAAGGTAGTTTTGATTTACACATACACAT TGGTGAAACAGTTGTAAATGTACTGTTACCTTTTGAGAAGGTAGTTTTGATTTACACATACACAT A T PCDH10 Ensembl:ENSG00000138650 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs996194638 Functional Loss SNV dbSNP153 33..33 33 - - - 19304 RMVar_ID_19304 Human_SNP_ID_490438541 A-to-I Human chr12 - 10161115 10161115 10161115 GTAGTGTGGGCAGGGCGCGGTGTCTCACGACTATAGTCCCACTACTTTGGGAGGCTTGGCCTACA GTAGTGTGGGCAGGGCGCGGTGTCTCACGACTGTAGTCCCACTACTTTGGGAGGCTTGGCCTACA T C OLR1 Ensembl:ENSG00000173391 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1347515277 Functional Loss SNV dbSNP153 33..33 33 - - - 19305 RMVar_ID_19305 Human_SNP_ID_490441204 A-to-I Human chr12 - 10171614 10171614 10171614 CTAATAAGTGGTAGAGCTAGGACTGTACCACAAACTCCCATTTATCCAGAATTCTATACATCGGA CTAATAAGTGGTAGAGCTAGGACTGTACCACAGACTCCCATTTATCCAGAATTCTATACATCGGA T C OLR1 Ensembl:ENSG00000173391 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1288974347 Functional Loss SNV dbSNP153 33..33 33 - - - 19306 RMVar_ID_19306 Human_SNP_ID_490441325 A-to-I Human chr12 - 10172098 10172098 10172098 TTTGTTGAAGTTCGTGACTGCTTCACTCTCTCATTCTTAGCTTGAATTTGGAAATGACTTTTGAT TTTGTTGAAGTTCGTGACTGCTTCACTCTCTCGTTCTTAGCTTGAATTTGGAAATGACTTTTGAT T C OLR1 Ensembl:ENSG00000173391 Protein coding 5'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs912071512 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_37045 Human_Splice_Rec_1338521,Human_Splice_Rec_1338531,Human_Splice_Rec_1338543,Human_Splice_Rec_1338551 19307 RMVar_ID_19307 Human_SNP_ID_490441331 A-to-I Human chr12 - 10172106 10172106 10172106 ATTTTTAGTTTGTTGAAGTTCGTGACTGCTTCACTCTCTCATTCTTAGCTTGAATTTGGAAATGA ATTTTTAGTTTGTTGAAGTTCGTGACTGCTTCGCTCTCTCATTCTTAGCTTGAATTTGGAAATGA T C OLR1 Ensembl:ENSG00000173391 Protein coding 5'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs757079524 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_37045 19308 RMVar_ID_19308 Human_SNP_ID_490453622 A-to-I Human chr12 + 10216296 10216296 10216296 CGGAGGCTGAGGCAGGAGAATCGCTTGAGCCCAGGAGGTGGAGGTTGCAGTGATCCGAGATCAGG CGGAGGCTGAGGCAGGAGAATCGCTTGAGCCCGGGAGGTGGAGGTTGCAGTGATCCGAGATCAGG A G GABARAPL1 Ensembl:ENSG00000139112 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167649912 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66770 19309 RMVar_ID_19309 Human_SNP_ID_490454009 A-to-I Human chr12 + 10217503 10217503 10217503 TCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGCAGATCACTTGAAGTCAGGAGTTTGAGACC TCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGCAGATCACTTGAAGTCAGGAGTTTGAGACC A G GABARAPL1 Ensembl:ENSG00000139112 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs985927269 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66770 19310 RMVar_ID_19310 Human_SNP_ID_490454010 A-to-I Human chr12 + 10217507 10217507 10217507 TAATCCCAGCACTTTGGGAGGCCAAGGCAGGCAGATCACTTGAAGTCAGGAGTTTGAGACCAGCC TAATCCCAGCACTTTGGGAGGCCAAGGCAGGCGGATCACTTGAAGTCAGGAGTTTGAGACCAGCC A G GABARAPL1 Ensembl:ENSG00000139112 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1017365179 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66770 19311 RMVar_ID_19311 Human_SNP_ID_490579976 A-to-I Human chr12 - 10715463 10715463 10715463 TGGTTCACTGCAACTTCCACCATCCAGGTTCAAGTGATTCCTCTGCCTCAGTCTCCCTAATAGCT TGGTTCACTGCAACTTCCACCATCCAGGTTCAGGTGATTCCTCTGCCTCAGTCTCCCTAATAGCT T C YBX3 Ensembl:ENSG00000060138 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935425730 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63420,RMVar_hsa_circ_154863,RMVar_hsa_circ_319054,RMVar_hsa_circ_299135,RMVar_hsa_circ_339477,RMVar_hsa_circ_154864 19312 RMVar_ID_19312 Human_SNP_ID_490579991 A-to-I Human chr12 - 10715542 10715542 10715542 GTGACTTTTAAACAGAATTTTTTTTTTTTTTAAGATGGGGTCTCCCTCTTGCCCAGGCTGGAGTG GTGACTTTTAAACAGAATTTTTTTTTTTTTTAGGATGGGGTCTCCCTCTTGCCCAGGCTGGAGTG T C YBX3 Ensembl:ENSG00000060138 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs911796211 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63420,RMVar_hsa_circ_154863,RMVar_hsa_circ_319054,RMVar_hsa_circ_299135,RMVar_hsa_circ_339477,RMVar_hsa_circ_154864 19313 RMVar_ID_19313 Human_SNP_ID_490580917 A-to-I Human chr12 - 10719118 10719118 10719118 ATTTTAGCCACCAAAGTCCTTGGCACTGTCAAATGGTTCAACGTCAGAAATGGATATGGATTTAT ATTTTAGCCACCAAAGTCCTTGGCACTGTCAAGTGGTTCAACGTCAGAAATGGATATGGATTTAT T C YBX3 Ensembl:ENSG00000060138 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1184071039 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_872935,Human_RBP_ID_22646210 Human_Splice_Rec_1339490,Human_Splice_Rec_1339491,Human_Splice_Rec_1339506,Human_Splice_Rec_1339507,Human_Splice_Rec_1339524,Human_Splice_Rec_1339525,Human_Splice_Rec_1339616,Human_Splice_Rec_1339617,Human_Splice_Rec_1339628,Human_Splice_Rec_1339629,Human_Splice_Rec_1339634,Human_Splice_Rec_1339635 RMVar_hsa_circ_63420,RMVar_hsa_circ_339477 19314 RMVar_ID_19314 Human_SNP_ID_490642759 A-to-I Human chr12 - 10969885 10969885 10969885 GATGCAAGGAGAATTGCTTGAACCTGGGAGTCAGAGGTTGCAGTGAGCCGAGATTGTACCATGGC GATGCAAGGAGAATTGCTTGAACCTGGGAGTCGGAGGTTGCAGTGAGCCGAGATTGTACCATGGC T C AC018630.2,PRH1,TAS2R14 Ensembl:ENSG00000275778,Ensembl:ENSG00000231887,Ensembl:ENSG00000212127 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs777629225 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47991 19315 RMVar_ID_19315 Human_SNP_ID_490642772 A-to-I Human chr12 - 10969938 10969938 10969938 AAATTAGCCGGGTGTGGTGGTGGATGCCTTTAATCCCAGCTACTCAGGAGGCTGATGCAAGGAGA AAATTAGCCGGGTGTGGTGGTGGATGCCTTTATTCCCAGCTACTCAGGAGGCTGATGCAAGGAGA T A AC018630.2,PRH1,TAS2R14 Ensembl:ENSG00000275778,Ensembl:ENSG00000231887,Ensembl:ENSG00000212127 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1429313603 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11809172,Human_RBP_ID_24929082 RMVar_hsa_circ_47991 19316 RMVar_ID_19316 Human_SNP_ID_490654048 A-to-I Human chr12 - 11015971 11015971 11015971 CTTTGGTCTGCAAATTGACTGTCAATTCTCAGAAGAGATCTGTCTTGCTGCACATAGTTAGAAGA CTTTGGTCTGCAAATTGACTGTCAATTCTCAGGAGAGATCTGTCTTGCTGCACATAGTTAGAAGA T C AC018630.2,PRH1,TAS2R14 Ensembl:ENSG00000275778,Ensembl:ENSG00000231887,Ensembl:ENSG00000212127 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1310606334 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17561021 RMVar_hsa_circ_105061,RMVar_hsa_circ_290938,RMVar_hsa_circ_154871,RMVar_hsa_circ_154872,RMVar_hsa_circ_154874 19317 RMVar_ID_19317 Human_SNP_ID_490654146 A-to-I Human chr12 - 11016361 11016361 11016361 GTTGCTGGCCGCATGCAGTGTCCAGTTAACAAAAGTGAGGTCTGGTACAAAAGTAATGAATTTAT GTTGCTGGCCGCATGCAGTGTCCAGTTAACAAGAGTGAGGTCTGGTACAAAAGTAATGAATTTAT T C AC018630.2,PRH1,TAS2R14 Ensembl:ENSG00000275778,Ensembl:ENSG00000231887,Ensembl:ENSG00000212127 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1221567665 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105061,RMVar_hsa_circ_290938,RMVar_hsa_circ_154871,RMVar_hsa_circ_154872,RMVar_hsa_circ_154874 19318 RMVar_ID_19318 Human_SNP_ID_490654921 A-to-I Human chr12 - 11018689 11018689 11018689 GCTGTCCTGCTCATTTCCTTCCCTACTTTATAAAACGTTCACTTTCTGCTCCAAAGATGAAGTGT GCTGTCCTGCTCATTTCCTTCCCTACTTTATACAACGTTCACTTTCTGCTCCAAAGATGAAGTGT T G AC018630.2,PRH1,TAS2R14 Ensembl:ENSG00000275778,Ensembl:ENSG00000231887,Ensembl:ENSG00000212127 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1180701263 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17561026 RMVar_hsa_circ_105061,RMVar_hsa_circ_290938,RMVar_hsa_circ_154871,RMVar_hsa_circ_154872,RMVar_hsa_circ_154874 19319 RMVar_ID_19319 Human_SNP_ID_490655025 A-to-I Human chr12 - 11018929 11018929 11018929 TTTCTACTTAACTTTTTAGACATGCACATAGAACTGTTTACTTTCCCCCCACCAGACAGTCCCTT TTTCTACTTAACTTTTTAGACATGCACATAGACCTGTTTACTTTCCCCCCACCAGACAGTCCCTT T G AC018630.2,PRH1,TAS2R14 Ensembl:ENSG00000275778,Ensembl:ENSG00000231887,Ensembl:ENSG00000212127 Protein coding,Protein coding,Protein coding intron,intron,intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1307202137 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11810546,Human_RBP_ID_19718121 RMVar_hsa_circ_105061,RMVar_hsa_circ_290938,RMVar_hsa_circ_154871,RMVar_hsa_circ_154872,RMVar_hsa_circ_154874 19320 RMVar_ID_19320 Human_SNP_ID_490657816 A-to-I Human chr12 - 11026104 11026104 11026104 TTGAGCGCAGGAGTTCCAGGCTGCAGTGGACTATGATCCTGCCACTGTACTCCAGCTTGGGTAAC TTGAGCGCAGGAGTTCCAGGCTGCAGTGGACTGTGATCCTGCCACTGTACTCCAGCTTGGGTAAC T C AC018630.2,PRH1,TAS2R14 Ensembl:ENSG00000275778,Ensembl:ENSG00000231887,Ensembl:ENSG00000212127 Protein coding,Protein coding,Protein coding intron,intron,intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1427252251 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25018637 RMVar_hsa_circ_105061,RMVar_hsa_circ_290938,RMVar_hsa_circ_154871,RMVar_hsa_circ_154872,RMVar_hsa_circ_154874 19321 RMVar_ID_19321 Human_SNP_ID_490657826 A-to-I Human chr12 - 11026147 11026147 11026147 CCTATAGTTCCAAATACTTGGGAAGCTGAGGCAGGAGGATTGCTTGAGCGCAGGAGTTCCAGGCT CCTATAGTTCCAAATACTTGGGAAGCTGAGGCGGGAGGATTGCTTGAGCGCAGGAGTTCCAGGCT T C AC018630.2,PRH1,TAS2R14 Ensembl:ENSG00000275778,Ensembl:ENSG00000231887,Ensembl:ENSG00000212127 Protein coding,Protein coding,Protein coding intron,intron,intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1461339959 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105061,RMVar_hsa_circ_290938,RMVar_hsa_circ_154871,RMVar_hsa_circ_154872,RMVar_hsa_circ_154874 19322 RMVar_ID_19322 Human_SNP_ID_490657827 A-to-I Human chr12 - 11026147 11026147 11026147 CCTATAGTTCCAAATACTTGGGAAGCTGAGGCAGGAGGATTGCTTGAGCGCAGGAGTTCCAGGCT CCTATAGTTCCAAATACTTGGGAAGCTGAGGCCGGAGGATTGCTTGAGCGCAGGAGTTCCAGGCT T G AC018630.2,PRH1,TAS2R14 Ensembl:ENSG00000275778,Ensembl:ENSG00000231887,Ensembl:ENSG00000212127 Protein coding,Protein coding,Protein coding intron,intron,intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1461339959 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105061,RMVar_hsa_circ_290938,RMVar_hsa_circ_154871,RMVar_hsa_circ_154872,RMVar_hsa_circ_154874 19323 RMVar_ID_19323 Human_SNP_ID_490690238 A-to-I Human chr12 - 11128597 11128597 11128597 GGATTATAGGTGCGTGCCACCACCACCTGGCTAATTTTTATATTTTTAGTGGAGACAGGGTTTCA GGATTATAGGTGCGTGCCACCACCACCTGGCTGATTTTTATATTTTTAGTGGAGACAGGGTTTCA T C AC018630.2,PRH1,TAS2R14 Ensembl:ENSG00000275778,Ensembl:ENSG00000231887,Ensembl:ENSG00000212127 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1213532101 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9664146 RMVar_hsa_circ_112917,RMVar_hsa_circ_114046,RMVar_hsa_circ_154885,RMVar_hsa_circ_154886,RMVar_hsa_circ_154890,RMVar_hsa_circ_154891,RMVar_hsa_circ_154889 19324 RMVar_ID_19324 Human_SNP_ID_490690399 A-to-I Human chr12 - 11129043 11129043 11129043 TGGTACATGCCTATAGTTCCAAATAGTTGAGAAGCTGAGGCAGGAGGATTGCTTGAGCCCAGGAG TGGTACATGCCTATAGTTCCAAATAGTTGAGATGCTGAGGCAGGAGGATTGCTTGAGCCCAGGAG T A AC018630.2,PRH1,TAS2R14 Ensembl:ENSG00000275778,Ensembl:ENSG00000231887,Ensembl:ENSG00000212127 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1483540827 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112917,RMVar_hsa_circ_114046,RMVar_hsa_circ_154885,RMVar_hsa_circ_154886,RMVar_hsa_circ_154890,RMVar_hsa_circ_154891,RMVar_hsa_circ_154889 19325 RMVar_ID_19325 Human_SNP_ID_490690407 A-to-I Human chr12 - 11129063 11129063 11129063 TTAAAAATTACCTGGCATGGTGGTACATGCCTATAGTTCCAAATAGTTGAGAAGCTGAGGCAGGA TTAAAAATTACCTGGCATGGTGGTACATGCCTGTAGTTCCAAATAGTTGAGAAGCTGAGGCAGGA T C AC018630.2,PRH1,TAS2R14 Ensembl:ENSG00000275778,Ensembl:ENSG00000231887,Ensembl:ENSG00000212127 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1420701625 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112917,RMVar_hsa_circ_114046,RMVar_hsa_circ_154885,RMVar_hsa_circ_154886,RMVar_hsa_circ_154890,RMVar_hsa_circ_154891,RMVar_hsa_circ_154889 19326 RMVar_ID_19326 Human_SNP_ID_490708970 A-to-I Human chr12 + 11197173 11197173 11197173 AAACTCCTGACCTCAAGTGTTCCTCCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAG AAACTCCTGACCTCAAGTGTTCCTCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1486384975 Functional Loss SNV dbSNP153 33..33 33 - - - 19327 RMVar_ID_19327 Human_SNP_ID_490995047 A-to-I Human chr12 - 12253140 12253140 12253140 CCTGCCTCAGCCTCCTGGGTAGCTGGGATTACAGGCACGCGCCACCACGCCCTGCTAATTTTTAT CCTGCCTCAGCCTCCTGGGTAGCTGGGATTACGGGCACGCGCCACCACGCCCTGCTAATTTTTAT T C LRP6 Ensembl:ENSG00000070018 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1441459467 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107875,RMVar_hsa_circ_154938 19328 RMVar_ID_19328 Human_SNP_ID_491057114 A-to-I Human chr12 + 12473210 12473210 12473210 GCCCGGTTGGTCTCAAACTCCTGACCTCAGGTAATCCACCTGCCTTGGCCTCCCAAAGTGCTGGG GCCCGGTTGGTCTCAAACTCCTGACCTCAGGTGATCCACCTGCCTTGGCCTCCCAAAGTGCTGGG A G L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1209745004 Functional Loss SNV dbSNP153 33..33 33 - - - 19329 RMVar_ID_19329 Human_SNP_ID_491057115 A-to-I Human chr12 + 12473210 12473210 12473210 GCCCGGTTGGTCTCAAACTCCTGACCTCAGGTAATCCACCTGCCTTGGCCTCCCAAAGTGCTGGG GCCCGGTTGGTCTCAAACTCCTGACCTCAGGTTATCCACCTGCCTTGGCCTCCCAAAGTGCTGGG A T L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1209745004 Functional Loss SNV dbSNP153 33..33 33 - - - 19330 RMVar_ID_19330 Human_SNP_ID_491059996 A-to-I Human chr12 - 12483370 12483364 12483370 AAGAAAAAAAGTAAACCAAAAAGATAAAATAAAAATAAGTAAAATAGATAATGTCCATTGAACAC AAGAAAAAAAGTAAACCAAAAAGATAAAATAA______GTAAAATAGATAATGTCCATTGAACAC CTTATTT C DUSP16 Ensembl:ENSG00000111266 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1013208173 Functional Loss DEL dbSNP153 33..38 33 - - - RMVar_hsa_circ_154941,RMVar_hsa_circ_104645,RMVar_hsa_circ_376998,RMVar_hsa_circ_269417,RMVar_hsa_circ_154942 19331 RMVar_ID_19331 Human_SNP_ID_491069777 A-to-I Human chr12 - 12525701 12525701 12525701 GTATACATATATTTTTAATTTTTTGTAGAGATAGGGTCTCACTGTGTTGCTCAGGCTGGTCTTGA GTATACATATATTTTTAATTTTTTGTAGAGATGGGGTCTCACTGTGTTGCTCAGGCTGGTCTTGA T C DUSP16 Ensembl:ENSG00000111266 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs527895802 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97188,RMVar_hsa_circ_87930,RMVar_hsa_circ_154945,RMVar_hsa_circ_154947 19332 RMVar_ID_19332 Human_SNP_ID_491076402 A-to-I Human chr12 - 12552228 12552228 12552228 TTGACCAGGCTGGTCTCAAACTCCCGACCCCAAGTGATCCGCTTGCCTCGGCCTCCCAAATTTCT TTGACCAGGCTGGTCTCAAACTCCCGACCCCATGTGATCCGCTTGCCTCGGCCTCCCAAATTTCT T A DUSP16 Ensembl:ENSG00000111266 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1411115001 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97188,RMVar_hsa_circ_87930,RMVar_hsa_circ_154945,RMVar_hsa_circ_154947 19333 RMVar_ID_19333 Human_SNP_ID_491076412 A-to-I Human chr12 - 12552254 12552254 12552254 TTTAGTAGAGATGGGGTTTCAGCATATTGACCAGGCTGGTCTCAAACTCCCGACCCCAAGTGATC TTTAGTAGAGATGGGGTTTCAGCATATTGACCCGGCTGGTCTCAAACTCCCGACCCCAAGTGATC T G DUSP16 Ensembl:ENSG00000111266 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1341618926 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97188,RMVar_hsa_circ_87930,RMVar_hsa_circ_154945,RMVar_hsa_circ_154947 19334 RMVar_ID_19334 Human_SNP_ID_491076751 A-to-I Human chr12 - 12553645 12553645 12553645 CCAGCCACTCGTGGGGCTCAGGTAGGAGGATCACCTGAGCCTGGCAGGTCAAGGCTGCAGTAAGC CCAGCCACTCGTGGGGCTCAGGTAGGAGGATCGCCTGAGCCTGGCAGGTCAAGGCTGCAGTAAGC T C DUSP16 Ensembl:ENSG00000111266 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1035007593 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17561042 RMVar_hsa_circ_97188,RMVar_hsa_circ_87930,RMVar_hsa_circ_154945,RMVar_hsa_circ_154947 19335 RMVar_ID_19335 Human_SNP_ID_491077319 A-to-I Human chr12 - 12555885 12555885 12555885 AGGCATGTGCAACTATACCTAGCTAATTTTTTATTTTGTGTAGAGACAGGGTCTTGCTATGTTGC AGGCATGTGCAACTATACCTAGCTAATTTTTTGTTTTGTGTAGAGACAGGGTCTTGCTATGTTGC T C DUSP16 Ensembl:ENSG00000111266 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs937588981 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2312746,Human_RBP_ID_11873415 RMVar_hsa_circ_97188,RMVar_hsa_circ_87930,RMVar_hsa_circ_154945,RMVar_hsa_circ_154947 19336 RMVar_ID_19336 Human_SNP_ID_491094929 A-to-I Human chr12 + 12620450 12620450 12620450 TAGAGACAGCCTGTGTTGTCCAGGCTGGTTTCAGACTCCCAAGCTCAAGCAATCTGCCCGCCTCT TAGAGACAGCCTGTGTTGTCCAGGCTGGTTTCTGACTCCCAAGCTCAAGCAATCTGCCCGCCTCT A T CREBL2 Ensembl:ENSG00000111269 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs915769344 Functional Loss SNV dbSNP153 33..33 33 - - - 19337 RMVar_ID_19337 Human_SNP_ID_491121086 A-to-I Human chr12 + 12728456 12728456 12728456 GGGAGGCTGAGGCGGGCAGATCGCTTGAACTCAGGAGTTCTGGACCAGCCTGGGCAACATGGTGA GGGAGGCTGAGGCGGGCAGATCGCTTGAACTCGGGAGTTCTGGACCAGCCTGGGCAACATGGTGA A G APOLD1 Ensembl:ENSG00000178878 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs940703920 Functional Loss SNV dbSNP153 33..33 33 - - - 19338 RMVar_ID_19338 Human_SNP_ID_491121523 A-to-I Human chr12 + 12729892 12729892 12729892 ATACAACTACTGGGACATTTTTTTTTGAGACCAGGTCTCACTCTGTTACCTAGGCTGGAGTGCAA ATACAACTACTGGGACATTTTTTTTTGAGACCGGGTCTCACTCTGTTACCTAGGCTGGAGTGCAA A G APOLD1 Ensembl:ENSG00000178878 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1186833074 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2312977 19339 RMVar_ID_19339 Human_SNP_ID_491121762 A-to-I Human chr12 + 12730497 12730497 12730497 GAGGTCAGGAATTGGAGACCAGTCTGGACAACATGGTGAAACCCCATCTCTACTAAAAATACAAA GAGGTCAGGAATTGGAGACCAGTCTGGACAACGTGGTGAAACCCCATCTCTACTAAAAATACAAA A G APOLD1 Ensembl:ENSG00000178878 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs578073100 Functional Loss SNV dbSNP153 33..33 33 - - - 19340 RMVar_ID_19340 Human_SNP_ID_491127019 A-to-I Human chr12 + 12751023 12751023 12751023 GTTGCCCCAGCTGTTGTTGAACTCCTGGGCTCAAGCAATCCACTTGCCTTAGCCTCCCAAATTGT GTTGCCCCAGCTGTTGTTGAACTCCTGGGCTCCAGCAATCCACTTGCCTTAGCCTCCCAAATTGT A C APOLD1 Ensembl:ENSG00000178878 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs972945512 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23156825 19341 RMVar_ID_19341 Human_SNP_ID_491127592 A-to-I Human chr12 + 12753410 12753410 12753410 GAAGGGGGTTGGGTGTGATGGCTCATGCCCGTAATCCCAAAACTTTGGGAGGCCAAGGAAGGATA GAAGGGGGTTGGGTGTGATGGCTCATGCCCGTGATCCCAAAACTTTGGGAGGCCAAGGAAGGATA A G APOLD1 Ensembl:ENSG00000178878 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs12816360 Functional Loss SNV dbSNP153 33..33 33 - - - 19342 RMVar_ID_19342 Human_SNP_ID_491128456 A-to-I Human chr12 + 12756911 12756911 12756911 CGGGTTCAAGTGATTCTCCTGCCTCTGTCTCCAGAGTAGCTGGGATTACAGGCGCCCACCACCAG CGGGTTCAAGTGATTCTCCTGCCTCTGTCTCCGGAGTAGCTGGGATTACAGGCGCCCACCACCAG A G APOLD1 Ensembl:ENSG00000178878 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs532645713 Functional Loss SNV dbSNP153 33..33 33 - - - 19343 RMVar_ID_19343 Human_SNP_ID_491130853 A-to-I Human chr12 + 12767090 12767090 12767090 AAATATGGTGAAACCTCATCTCTATTAAAAATACAAAAATCAGCCGGGTGTGGTGGTGCATGCCT AAATATGGTGAAACCTCATCTCTATTAAAAATGCAAAAATCAGCCGGGTGTGGTGGTGCATGCCT A G APOLD1 Ensembl:ENSG00000178878 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs751971660 Functional Loss SNV dbSNP153 33..33 33 - - - 19344 RMVar_ID_19344 Human_SNP_ID_491131663 A-to-I Human chr12 + 12770203 12770203 12770203 AGGCCGAGGCGGGCAGATCACGAAGTCAGTTCAAGACCAGCCTGACAAGCATGGTGAAACCTCGT AGGCCGAGGCGGGCAGATCACGAAGTCAGTTCGAGACCAGCCTGACAAGCATGGTGAAACCTCGT A G APOLD1 Ensembl:ENSG00000178878 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs546605444 Functional Loss SNV dbSNP153 33..33 33 - - - 19345 RMVar_ID_19345 Human_SNP_ID_491136747 A-to-I Human chr12 + 12790103 12790103 12790103 TCGGCTCACTGCAACCTCCGACTCCTGGGTTCAAGCAATTCTTCTGCCTCAGCCTCCTGAGTAGC TCGGCTCACTGCAACCTCCGACTCCTGGGTTCCAGCAATTCTTCTGCCTCAGCCTCCTGAGTAGC A C APOLD1 Ensembl:ENSG00000178878 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs536960275 Functional Loss SNV dbSNP153 33..33 33 - - - 19346 RMVar_ID_19346 Human_SNP_ID_491138580 A-to-I Human chr12 + 12797359 12797359 12797359 TGGAGTTCAGTGGCATGATCTCAGCTCACTGTAACCTTTGCCTCCCGAGTTCAAGCAATTTTCCT TGGAGTTCAGTGGCATGATCTCAGCTCACTGTGACCTTTGCCTCCCGAGTTCAAGCAATTTTCCT A G APOLD1 Ensembl:ENSG00000178878 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985246166 Functional Loss SNV dbSNP153 33..33 33 - - - 19347 RMVar_ID_19347 Human_SNP_ID_491138581 A-to-I Human chr12 + 12797359 12797359 12797359 TGGAGTTCAGTGGCATGATCTCAGCTCACTGTAACCTTTGCCTCCCGAGTTCAAGCAATTTTCCT TGGAGTTCAGTGGCATGATCTCAGCTCACTGTTACCTTTGCCTCCCGAGTTCAAGCAATTTTCCT A T APOLD1 Ensembl:ENSG00000178878 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985246166 Functional Loss SNV dbSNP153 33..33 33 - - - 19348 RMVar_ID_19348 Human_SNP_ID_491152672 A-to-I Human chr12 + 12851099 12851099 12851099 AGAAGCTTATGGCCACAGAAGTTGCTGCTGACACTCTGGGTGAAGAATGGAAAGGTTATGTGGTC AGAAGCTTATGGCCACAGAAGTTGCTGCTGACGCTCTGGGTGAAGAATGGAAAGGTTATGTGGTC A G AC007688.2 Ensembl:ENSG00000241352 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878890930 Functional Loss SNV dbSNP153 33..33 33 - - - 19349 RMVar_ID_19349 Human_SNP_ID_491165525 A-to-I Human chr12 + 12898352 12898352 12898352 CCTCAGGAGTTGAAGAGCTGCCTGGGCAACATAGCGAGACCCCACCTCTACAAAAAATACAAAAA CCTCAGGAGTTGAAGAGCTGCCTGGGCAACATTGCGAGACCCCACCTCTACAAAAAATACAAAAA A T GPRC5A Ensembl:ENSG00000013588 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1475245493 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118946,RMVar_hsa_circ_154958,RMVar_hsa_circ_76214,RMVar_hsa_circ_154957 19350 RMVar_ID_19350 Human_SNP_ID_491178990 A-to-I Human chr12 + 12944235 12944235 12944235 AAGTGATCCATCTCACGGCCTCTTGAGTAGCTAGGACCACAGGTGTGTGCCACTATGTCCAGCTA AAGTGATCCATCTCACGGCCTCTTGAGTAGCTGGGACCACAGGTGTGTGCCACTATGTCCAGCTA A G GPRC5D-AS1 Ensembl:ENSG00000247498 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1410598182 Functional Loss SNV dbSNP153 33..33 33 - - - 19351 RMVar_ID_19351 Human_SNP_ID_491184460 A-to-I Human chr12 + 12961699 12961699 12961699 ATGATCTCAGTTCACTGCAGCTTCGACTTCCTAGGCTCAAGTGATCCTCCCACCTTAGCCTCCCA ATGATCTCAGTTCACTGCAGCTTCGACTTCCTCGGCTCAAGTGATCCTCCCACCTTAGCCTCCCA A C GPRC5D-AS1 Ensembl:ENSG00000247498 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs936806016 Functional Loss SNV dbSNP153 33..33 33 - - - 19352 RMVar_ID_19352 Human_SNP_ID_491402755 A-to-I Human chr12 - 13860556 13860556 13860556 ACTTTGGAGGCGGAGGCAGGCAGATCACCCTAAGTAAGGAGTTCGAGACCATTCTGGCCAACATG ACTTTGGAGGCGGAGGCAGGCAGATCACCCTAGGTAAGGAGTTCGAGACCATTCTGGCCAACATG T C GRIN2B Ensembl:ENSG00000273079 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs537623518 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49875,RMVar_hsa_circ_22169 19353 RMVar_ID_19353 Human_SNP_ID_491533850 A-to-I Human chr12 + 14377669 14377669 14377669 AGAGTCTCGCTCTGTCACCCACGTTGGAGTGCAATGGCGTGATCTCGGCTCACTCCAGTCTCTGC AGAGTCTCGCTCTGTCACCCACGTTGGAGTGCGATGGCGTGATCTCGGCTCACTCCAGTCTCTGC A G ATF7IP Ensembl:ENSG00000171681 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs975326960 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11889245 19354 RMVar_ID_19354 Human_SNP_ID_491545418 A-to-I Human chr12 + 14426034 14426034 14426034 CATTTGCTCCCTCAGCCCTTTTGATTCTACCCAACCTATTCTCTTCCTCATTTTCTGAATGAGCT CATTTGCTCCCTCAGCCCTTTTGATTCTACCCGACCTATTCTCTTCCTCATTTTCTGAATGAGCT A G ATF7IP Ensembl:ENSG00000171681 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1315447382 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71272,RMVar_hsa_circ_271816,RMVar_hsa_circ_353304,RMVar_hsa_circ_283886,RMVar_hsa_circ_73334,RMVar_hsa_circ_154989,RMVar_hsa_circ_60825,RMVar_hsa_circ_68597,RMVar_hsa_circ_154991,RMVar_hsa_circ_60089,RMVar_hsa_circ_154990 19355 RMVar_ID_19355 Human_SNP_ID_491545543 A-to-I Human chr12 + 14426569 14426569 14426569 TTTTTTTTGGCCAGGTAAGGTGGCTCACACCTATAATCCTAGGACTTTGGGAGGCTGAGGCAGGC TTTTTTTTGGCCAGGTAAGGTGGCTCACACCTGTAATCCTAGGACTTTGGGAGGCTGAGGCAGGC A G ATF7IP Ensembl:ENSG00000171681 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1388151301 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71272,RMVar_hsa_circ_271816,RMVar_hsa_circ_353304,RMVar_hsa_circ_283886,RMVar_hsa_circ_73334,RMVar_hsa_circ_154989,RMVar_hsa_circ_60825,RMVar_hsa_circ_68597,RMVar_hsa_circ_154991,RMVar_hsa_circ_60089,RMVar_hsa_circ_154990 19356 RMVar_ID_19356 Human_SNP_ID_491550699 A-to-I Human chr12 + 14447303 14447303 14447303 TTATGCAATTCTTTTTTTTTTTTTTTTTTTTGAGATGGAGTCTCTCTGTCGCCCAGGCTGGAGTG TTATGCAATTCTTTTTTTTTTTTTTTTTTTTGTGATGGAGTCTCTCTGTCGCCCAGGCTGGAGTG A T ATF7IP Ensembl:ENSG00000171681 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215486640 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_353304,RMVar_hsa_circ_73334,RMVar_hsa_circ_30434,RMVar_hsa_circ_8806,RMVar_hsa_circ_68597,RMVar_hsa_circ_154991,RMVar_hsa_circ_60089,RMVar_hsa_circ_28496,RMVar_hsa_circ_50948,RMVar_hsa_circ_8584,RMVar_hsa_circ_301117,RMVar_hsa_circ_321609,RMVar_hsa_circ_155000 19357 RMVar_ID_19357 Human_SNP_ID_491626077 A-to-I Human chr12 - 14764639 14764639 14764639 CAGAGTTTCCCTATTGTCACCCAGGATGGAGTACAGTGGCACGATCTCGGCTCACTGCAACCTCC CAGAGTTTCCCTATTGTCACCCAGGATGGAGTGCAGTGGCACGATCTCGGCTCACTGCAACCTCC T C AC010168.2 Ensembl:ENSG00000261324 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048663832 Functional Loss SNV dbSNP153 33..33 33 - - - 19358 RMVar_ID_19358 Human_SNP_ID_491806250 A-to-I Human chr12 + 15512943 15512943 15512943 GTGAACCCAGGAGGCAGAGGTTGCAGTGAGCCAAGATCGTGCCACTGCACTCCAGGTTGGGCAAC GTGAACCCAGGAGGCAGAGGTTGCAGTGAGCCGAGATCGTGCCACTGCACTCCAGGTTGGGCAAC A G PTPRO Ensembl:ENSG00000151490 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1457889335 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_322809,RMVar_hsa_circ_346372,RMVar_hsa_circ_35434,RMVar_hsa_circ_43751,RMVar_hsa_circ_49963,RMVar_hsa_circ_155029,RMVar_hsa_circ_155031,RMVar_hsa_circ_155030,RMVar_hsa_circ_32534,RMVar_hsa_circ_378169,RMVar_hsa_circ_155036,RMVar_hsa_circ_283279,RMVar_hsa_circ_321436,RMVar_hsa_circ_322376,RMVar_hsa_circ_328148,RMVar_hsa_circ_341613,RMVar_hsa_circ_326998,RMVar_hsa_circ_321669,RMVar_hsa_circ_319098,RMVar_hsa_circ_286434,RMVar_hsa_circ_96383,RMVar_hsa_circ_282638,RMVar_hsa_circ_50080,RMVar_hsa_circ_155040,RMVar_hsa_circ_155044,RMVar_hsa_circ_155046,RMVar_hsa_circ_155048,RMVar_hsa_circ_155050,RMVar_hsa_circ_155049,RMVar_hsa_circ_155047,RMVar_hsa_circ_155045,RMVar_hsa_circ_155042,RMVar_hsa_circ_155043,RMVar_hsa_circ_155041,RMVar_hsa_circ_15906,RMVar_hsa_circ_50123 19359 RMVar_ID_19359 Human_SNP_ID_491833102 A-to-I Human chr12 - 15620679 15620679 15620679 GTCATGGCTCTGTTGATTGCAACTCCTTGTATAGCTTGTATTTTGATTTAGTTTATATTCTGCTT GTCATGGCTCTGTTGATTGCAACTCCTTGTATGGCTTGTATTTTGATTTAGTTTATATTCTGCTT T C EPS8 Ensembl:ENSG00000151491 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1430177973 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_415924 RMVar_hsa_circ_155062 19360 RMVar_ID_19360 Human_SNP_ID_491906294 A-to-I Human chr12 + 15935366 15935361 15935367 AAAATTAGCCAGGTGTGGTGGCATCCACCTGTAGTCCTACCTACTTGGGAGGCTGAGCTGGGAGG AAAATTAGCCAGGTGTGGTGGCATCCAC______TCCTACCTACTTGGGAGGCTGAGCTGGGAGG CCTGTAG C DERA Ensembl:ENSG00000023697 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348193332 Functional Loss DEL dbSNP153 29..34 33 - - - RMVar_hsa_circ_35249,RMVar_hsa_circ_20004 19361 RMVar_ID_19361 Human_SNP_ID_491917544 A-to-I Human chr12 + 15981195 15981195 15981195 ACGGTGAAACCCCGTCTCTACTAAAACTACAAAAAGTTACCCAGGCGTGGTGGCAGGCGCCTGTA ACGGTGAAACCCCGTCTCTACTAAAACTACAAGAAGTTACCCAGGCGTGGTGGCAGGCGCCTGTA A G DERA Ensembl:ENSG00000023697 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1286594900 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20004,RMVar_hsa_circ_292981,RMVar_hsa_circ_118870,RMVar_hsa_circ_10089,RMVar_hsa_circ_155092,RMVar_hsa_circ_155093,RMVar_hsa_circ_61931 19362 RMVar_ID_19362 Human_SNP_ID_492020188 A-to-I Human chr12 + 16400229 16400229 16400229 CACTTCTGTGTAGAACTGCACATCCATGTGCCACTTCTTCCCAAACATGATGGCATTCTTGAGGT CACTTCTGTGTAGAACTGCACATCCATGTGCCGCTTCTTCCCAAACATGATGGCATTCTTGAGGT A G MGST1 Ensembl:ENSG00000008394 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1287855694 Functional Loss SNV dbSNP153 33..33 33 - - - 19363 RMVar_ID_19363 Human_SNP_ID_492021907 A-to-I Human chr12 + 16407528 16407528 16407528 GCAGTGAGGCACTTCCTCAAAGAACTAAAAGCAGAACTACCATTTGACCCAGCAATCCCATTATT GCAGTGAGGCACTTCCTCAAAGAACTAAAAGCGGAACTACCATTTGACCCAGCAATCCCATTATT A G MGST1 Ensembl:ENSG00000008394 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs534780705 Functional Loss SNV dbSNP153 33..33 33 - - - 19364 RMVar_ID_19364 Human_SNP_ID_492039779 A-to-I Human chr12 + 16482361 16482360 16482362 GAAGTATAAAAAAAAGAGCAAGGGCCGGGTGCAGTGGCTCACGCCTGTAATCTTAGCACTTTAGG GAAGTATAAAAAAAAGAGCAAGGGCCGGGTGC__TGGCTCACGCCTGTAATCTTAGCACTTTAGG CAG C MGST1 Ensembl:ENSG00000008394 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs988154162 Functional Loss DEL dbSNP153 33..34 33 - - - 19365 RMVar_ID_19365 Human_SNP_ID_492039781 A-to-I Human chr12 + 16482361 16482361 16482361 GAAGTATAAAAAAAAGAGCAAGGGCCGGGTGCAGTGGCTCACGCCTGTAATCTTAGCACTTTAGG GAAGTATAAAAAAAAGAGCAAGGGCCGGGTGCGGTGGCTCACGCCTGTAATCTTAGCACTTTAGG A G MGST1 Ensembl:ENSG00000008394 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941705259 Functional Loss SNV dbSNP153 33..33 33 - - - 19366 RMVar_ID_19366 Human_SNP_ID_492039782 A-to-I Human chr12 + 16482361 16482361 16482361 GAAGTATAAAAAAAAGAGCAAGGGCCGGGTGCAGTGGCTCACGCCTGTAATCTTAGCACTTTAGG GAAGTATAAAAAAAAGAGCAAGGGCCGGGTGCTGTGGCTCACGCCTGTAATCTTAGCACTTTAGG A T MGST1 Ensembl:ENSG00000008394 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941705259 Functional Loss SNV dbSNP153 33..33 33 - - - 19367 RMVar_ID_19367 Human_SNP_ID_492261723 A-to-I Human chr12 - 17400695 17400695 17400695 AGTGGGCCACTGCAGGCTACCAGCACAGCCCCAGTCAATGCTCCACTGGTAATAGATTTCCAGGG AGTGGGCCACTGCAGGCTACCAGCACAGCCCCCGTCAATGCTCCACTGGTAATAGATTTCCAGGG T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1321583065 Functional Loss SNV dbSNP153 33..33 33 - - - 19368 RMVar_ID_19368 Human_SNP_ID_492752433 A-to-I Human chr12 + 19248129 19248129 19248129 CCTTTAGTCCCAGCTACTTGAGAGGCTGAGGTAAGAGGACTGCATGAACTTGGGAGGTTGAGGCT CCTTTAGTCCCAGCTACTTGAGAGGCTGAGGTGAGAGGACTGCATGAACTTGGGAGGTTGAGGCT A G PLEKHA5 Ensembl:ENSG00000052126 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569975004 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43398,RMVar_hsa_circ_65865,RMVar_hsa_circ_350173,RMVar_hsa_circ_51755,RMVar_hsa_circ_34460 19369 RMVar_ID_19369 Human_SNP_ID_492755291 A-to-I Human chr12 + 19259283 19259283 19259283 CCAGCTACTCCGGAGGCTGAAGTGGGAGGATCACTTGAGCCCAGGATTTGAGCTTGCAGTGAGGT CCAGCTACTCCGGAGGCTGAAGTGGGAGGATCGCTTGAGCCCAGGATTTGAGCTTGCAGTGAGGT A G PLEKHA5 Ensembl:ENSG00000052126 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs544165152 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_155109,RMVar_hsa_circ_292123,RMVar_hsa_circ_43398,RMVar_hsa_circ_65865,RMVar_hsa_circ_350173,RMVar_hsa_circ_51755,RMVar_hsa_circ_325526,RMVar_hsa_circ_354803,RMVar_hsa_circ_366665,RMVar_hsa_circ_368140,RMVar_hsa_circ_351358,RMVar_hsa_circ_305045,RMVar_hsa_circ_323439,RMVar_hsa_circ_71025,RMVar_hsa_circ_286264,RMVar_hsa_circ_274163,RMVar_hsa_circ_60967,RMVar_hsa_circ_69879,RMVar_hsa_circ_155111,RMVar_hsa_circ_155112,RMVar_hsa_circ_155110,RMVar_hsa_circ_155116,RMVar_hsa_circ_7436,RMVar_hsa_circ_155107,RMVar_hsa_circ_155108,RMVar_hsa_circ_275880,RMVar_hsa_circ_302882,RMVar_hsa_circ_47051,RMVar_hsa_circ_155118,RMVar_hsa_circ_4258,RMVar_hsa_circ_155119,RMVar_hsa_circ_155117,RMVar_hsa_circ_30686 19370 RMVar_ID_19370 Human_SNP_ID_492758598 A-to-I Human chr12 + 19272616 19272616 19272616 AAAATTAGCTAGGTGTGGTGGCGTGTACCTATAGTCCCGGCTGCTCGGGAGGCTGAGAGGGAAGG AAAATTAGCTAGGTGTGGTGGCGTGTACCTATTGTCCCGGCTGCTCGGGAGGCTGAGAGGGAAGG A T PLEKHA5 Ensembl:ENSG00000052126 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs908725891 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_155109,RMVar_hsa_circ_292123,RMVar_hsa_circ_43398,RMVar_hsa_circ_65865,RMVar_hsa_circ_350173,RMVar_hsa_circ_51755,RMVar_hsa_circ_325526,RMVar_hsa_circ_354803,RMVar_hsa_circ_366665,RMVar_hsa_circ_368140,RMVar_hsa_circ_351358,RMVar_hsa_circ_305045,RMVar_hsa_circ_323439,RMVar_hsa_circ_71025,RMVar_hsa_circ_60967,RMVar_hsa_circ_69879,RMVar_hsa_circ_155110,RMVar_hsa_circ_7436,RMVar_hsa_circ_155107,RMVar_hsa_circ_155108,RMVar_hsa_circ_302882,RMVar_hsa_circ_155118,RMVar_hsa_circ_155119,RMVar_hsa_circ_155117,RMVar_hsa_circ_72831,RMVar_hsa_circ_155120,RMVar_hsa_circ_103883,RMVar_hsa_circ_356362,RMVar_hsa_circ_155121,RMVar_hsa_circ_155123,RMVar_hsa_circ_155122,RMVar_hsa_circ_324656,RMVar_hsa_circ_327466,RMVar_hsa_circ_54863,RMVar_hsa_circ_155124,RMVar_hsa_circ_303111,RMVar_hsa_circ_335215,RMVar_hsa_circ_348444,RMVar_hsa_circ_326593,RMVar_hsa_circ_270931,RMVar_hsa_circ_155125,RMVar_hsa_circ_31056,RMVar_hsa_circ_63234,RMVar_hsa_circ_155126,RMVar_hsa_circ_155127 19371 RMVar_ID_19371 Human_SNP_ID_492766775 A-to-I Human chr12 + 19304284 19304284 19304284 AAAATTAGCCGGGCGTAGTAGTGGGCACCTGTAATCCCAGCTACTCACGAGGCTGAGGCAAGAGA AAAATTAGCCGGGCGTAGTAGTGGGCACCTGTGATCCCAGCTACTCACGAGGCTGAGGCAAGAGA A G PLEKHA5 Ensembl:ENSG00000052126 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs979872269 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8940,RMVar_hsa_circ_51755,RMVar_hsa_circ_354803,RMVar_hsa_circ_366665,RMVar_hsa_circ_368140,RMVar_hsa_circ_351358,RMVar_hsa_circ_71025,RMVar_hsa_circ_60967,RMVar_hsa_circ_69879,RMVar_hsa_circ_155119,RMVar_hsa_circ_72831,RMVar_hsa_circ_103883,RMVar_hsa_circ_155121,RMVar_hsa_circ_335215,RMVar_hsa_circ_348444,RMVar_hsa_circ_326593,RMVar_hsa_circ_155125,RMVar_hsa_circ_31056,RMVar_hsa_circ_13620,RMVar_hsa_circ_2004,RMVar_hsa_circ_326191,RMVar_hsa_circ_341001,RMVar_hsa_circ_352143,RMVar_hsa_circ_323251,RMVar_hsa_circ_72972,RMVar_hsa_circ_15042,RMVar_hsa_circ_48242,RMVar_hsa_circ_352056,RMVar_hsa_circ_368260,RMVar_hsa_circ_336487,RMVar_hsa_circ_72228,RMVar_hsa_circ_33458,RMVar_hsa_circ_12604,RMVar_hsa_circ_14296,RMVar_hsa_circ_9520,RMVar_hsa_circ_37486,RMVar_hsa_circ_155134 19372 RMVar_ID_19372 Human_SNP_ID_492774365 A-to-I Human chr12 + 19332865 19332865 19332865 CTTTGCAGAGATGGGATTTCACCATGTTGCCCAGGCTGGTCTCAGATTCCTGGGCTCAAGCGATC CTTTGCAGAGATGGGATTTCACCATGTTGCCCCGGCTGGTCTCAGATTCCTGGGCTCAAGCGATC A C PLEKHA5 Ensembl:ENSG00000052126 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs903890773 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8940,RMVar_hsa_circ_51755,RMVar_hsa_circ_366665,RMVar_hsa_circ_368140,RMVar_hsa_circ_351358,RMVar_hsa_circ_60967,RMVar_hsa_circ_69879,RMVar_hsa_circ_103883,RMVar_hsa_circ_155121,RMVar_hsa_circ_335215,RMVar_hsa_circ_348444,RMVar_hsa_circ_31056,RMVar_hsa_circ_155135,RMVar_hsa_circ_326191,RMVar_hsa_circ_341001,RMVar_hsa_circ_323251,RMVar_hsa_circ_72972,RMVar_hsa_circ_15042,RMVar_hsa_circ_48242,RMVar_hsa_circ_368260,RMVar_hsa_circ_336487,RMVar_hsa_circ_72228,RMVar_hsa_circ_33458,RMVar_hsa_circ_14296,RMVar_hsa_circ_9520,RMVar_hsa_circ_13432,RMVar_hsa_circ_48918,RMVar_hsa_circ_155136,RMVar_hsa_circ_155137,RMVar_hsa_circ_155141,RMVar_hsa_circ_305966,RMVar_hsa_circ_328791,RMVar_hsa_circ_330642,RMVar_hsa_circ_359294,RMVar_hsa_circ_313874,RMVar_hsa_circ_293372,RMVar_hsa_circ_155139,RMVar_hsa_circ_155140,RMVar_hsa_circ_155138,RMVar_hsa_circ_3987,RMVar_hsa_circ_268707,RMVar_hsa_circ_316344,RMVar_hsa_circ_357440,RMVar_hsa_circ_358168,RMVar_hsa_circ_41112 19373 RMVar_ID_19373 Human_SNP_ID_492797027 A-to-I Human chr12 + 19413167 19413167 19413167 CCCAAGTTTAGCCGACAGGATCCTGGCGATGCAGCCCAACAGGAAGCAAAGCACAGGGAAGCAGA CCCAAGTTTAGCCGACAGGATCCTGGCGATGCGGCCCAACAGGAAGCAAAGCACAGGGAAGCAGA A G AEBP2,PDCD5P1 Ensembl:ENSG00000139154,Ensembl:ENSG00000255909 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878907422 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4253487,Human_RBP_ID_18623666 19374 RMVar_ID_19374 Human_SNP_ID_492797028 A-to-I Human chr12 + 19413167 19413167 19413167 CCCAAGTTTAGCCGACAGGATCCTGGCGATGCAGCCCAACAGGAAGCAAAGCACAGGGAAGCAGA CCCAAGTTTAGCCGACAGGATCCTGGCGATGCTGCCCAACAGGAAGCAAAGCACAGGGAAGCAGA A T AEBP2,PDCD5P1 Ensembl:ENSG00000139154,Ensembl:ENSG00000255909 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878907422 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4253487,Human_RBP_ID_18623666 19375 RMVar_ID_19375 Human_SNP_ID_492804715 A-to-I Human chr12 + 19440814 19440814 19440814 TGTTTCCAATATGGCTGGTCTCGCCTGGATTTAACAGAACTTCCTTGTCCATGGGAGAGACCCCA TGTTTCCAATATGGCTGGTCTCGCCTGGATTTGACAGAACTTCCTTGTCCATGGGAGAGACCCCA A G AEBP2 Ensembl:ENSG00000139154 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1023390785 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126552,RMVar_hsa_circ_155163 19376 RMVar_ID_19376 Human_SNP_ID_492805452 A-to-I Human chr12 + 19443278 19443278 19443278 GCCACCACCCCTGGCTAATTTTTGTTTTTAGTAGAGATGCGATTTCACCATGTTGTCCAGGCTGG GCCACCACCCCTGGCTAATTTTTGTTTTTAGTGGAGATGCGATTTCACCATGTTGTCCAGGCTGG A G AEBP2 Ensembl:ENSG00000139154 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1294695134 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126552,RMVar_hsa_circ_155163 19377 RMVar_ID_19377 Human_SNP_ID_492807667 A-to-I Human chr12 + 19450783 19450783 19450783 AAGATCGTTTGAATCTGGGAAGTTGAGGCTGCAATGAACTATGATTGTGCCACTGTACTCCTGCC AAGATCGTTTGAATCTGGGAAGTTGAGGCTGCCATGAACTATGATTGTGCCACTGTACTCCTGCC A C AEBP2 Ensembl:ENSG00000139154 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs762993317 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11896591 RMVar_hsa_circ_126552,RMVar_hsa_circ_155163 19378 RMVar_ID_19378 Human_SNP_ID_492812333 A-to-I Human chr12 + 19466319 19466319 19466319 AAATCCTGTCTCTACAAAAATTAGCTGGGTGTAGTGGCACACGCCTGTGGTCTTAGCCACTCCGG AAATCCTGTCTCTACAAAAATTAGCTGGGTGTGGTGGCACACGCCTGTGGTCTTAGCCACTCCGG A G AEBP2 Ensembl:ENSG00000139154 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1271343874 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_155167,RMVar_hsa_circ_274817,RMVar_hsa_circ_126552,RMVar_hsa_circ_284475,RMVar_hsa_circ_155163,RMVar_hsa_circ_321001,RMVar_hsa_circ_277844,RMVar_hsa_circ_155169,RMVar_hsa_circ_270751,RMVar_hsa_circ_155168,RMVar_hsa_circ_155165,RMVar_hsa_circ_155166,RMVar_hsa_circ_155164 19379 RMVar_ID_19379 Human_SNP_ID_492821909 A-to-I Human chr12 + 19499388 19499388 19499388 TATACCCAGCACTTTTGGAGGCCGAGGTAGGCAGATCACATGAAGCCAGGAGTTCAAGACCAGCC TATACCCAGCACTTTTGGAGGCCGAGGTAGGCCGATCACATGAAGCCAGGAGTTCAAGACCAGCC A C AEBP2 Ensembl:ENSG00000139154 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1332028277 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_155171,RMVar_hsa_circ_321001,RMVar_hsa_circ_277844,RMVar_hsa_circ_270751,RMVar_hsa_circ_155165,RMVar_hsa_circ_155164,RMVar_hsa_circ_123942,RMVar_hsa_circ_155175,RMVar_hsa_circ_297572,RMVar_hsa_circ_155170,RMVar_hsa_circ_366803,RMVar_hsa_circ_298771,RMVar_hsa_circ_286160,RMVar_hsa_circ_155173,RMVar_hsa_circ_155174,RMVar_hsa_circ_321818,RMVar_hsa_circ_155172,RMVar_hsa_circ_155178,RMVar_hsa_circ_36296,RMVar_hsa_circ_155177 19380 RMVar_ID_19380 Human_SNP_ID_492825939 A-to-I Human chr12 + 19513642 19513642 19513642 AGAAATTAGCTGGTTGTGATGGTGTCGCCTGTAGTCCCAGATACTCAGGAGACTGAGGCGGGAAG AGAAATTAGCTGGTTGTGATGGTGTCGCCTGTCGTCCCAGATACTCAGGAGACTGAGGCGGGAAG A C AEBP2 Ensembl:ENSG00000139154 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs373500723 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11897719 RMVar_hsa_circ_321001,RMVar_hsa_circ_270751,RMVar_hsa_circ_155164,RMVar_hsa_circ_123942,RMVar_hsa_circ_297572,RMVar_hsa_circ_366803,RMVar_hsa_circ_155173,RMVar_hsa_circ_155172,RMVar_hsa_circ_155178,RMVar_hsa_circ_358662,RMVar_hsa_circ_155181,RMVar_hsa_circ_155182,RMVar_hsa_circ_313652 19381 RMVar_ID_19381 Human_SNP_ID_492825940 A-to-I Human chr12 + 19513642 19513642 19513642 AGAAATTAGCTGGTTGTGATGGTGTCGCCTGTAGTCCCAGATACTCAGGAGACTGAGGCGGGAAG AGAAATTAGCTGGTTGTGATGGTGTCGCCTGTGGTCCCAGATACTCAGGAGACTGAGGCGGGAAG A G AEBP2 Ensembl:ENSG00000139154 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs373500723 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11897719 RMVar_hsa_circ_321001,RMVar_hsa_circ_270751,RMVar_hsa_circ_155164,RMVar_hsa_circ_123942,RMVar_hsa_circ_297572,RMVar_hsa_circ_366803,RMVar_hsa_circ_155173,RMVar_hsa_circ_155172,RMVar_hsa_circ_155178,RMVar_hsa_circ_358662,RMVar_hsa_circ_155181,RMVar_hsa_circ_155182,RMVar_hsa_circ_313652 19382 RMVar_ID_19382 Human_SNP_ID_492830343 A-to-I Human chr12 + 19528574 19528574 19528574 CTCCTGCCTCAGGCTCCTGAGTAGCTGGGATTACAGGCATGCGCCACCATGCTCGGCTAATTTTG CTCCTGCCTCAGGCTCCTGAGTAGCTGGGATTTCAGGCATGCGCCACCATGCTCGGCTAATTTTG A T AEBP2 Ensembl:ENSG00000139154 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1003957395 Functional Loss SNV dbSNP153 33..33 33 - - - 19383 RMVar_ID_19383 Human_SNP_ID_492863957 A-to-I Human chr12 + 19660312 19660312 19660312 TGATGAGCCCTCATGACTTAATCACCTCTTAAAATCCCACCTCTTAATACTGTTACAAAGGCAAT TGATGAGCCCTCATGACTTAATCACCTCTTAACATCCCACCTCTTAATACTGTTACAAAGGCAAT A C AEBP2 Ensembl:ENSG00000139154 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474908663 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_155186 19384 RMVar_ID_19384 Human_SNP_ID_492867347 A-to-I Human chr12 + 19674843 19674842 19674843 AGGAGTTCAACATGGTGAAACCCCATCTCTACAAAAAATACAAAAATTAGCCGAGTATGGTAGCA AGGAGTTCAACATGGTGAAACCCCATCTCTAC_AAAAATACAAAAATTAGCCGAGTATGGTAGCA CA C AEBP2 Ensembl:ENSG00000139154 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1399679291 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_155186 19385 RMVar_ID_19385 Human_SNP_ID_492879975 A-to-I Human chr12 + 19724230 19724230 19724230 GAAGCTGGACCCCTTCCTTACACTGTATACAAAATCAACTCAAGAGGGTTAAGGACTTAAATGTA GAAGCTGGACCCCTTCCTTACACTGTATACAATATCAACTCAAGAGGGTTAAGGACTTAAATGTA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1315762582 Functional Loss SNV dbSNP153 33..33 33 - - - 19386 RMVar_ID_19386 Human_SNP_ID_271638885 A-to-I Human chr6 - 30200241 30200241 30200241 CTCTTATTCTGTTGCCCAGTCTGGAGTGTAGTAGTACAATCATGGCTCACTGTAGCCTCCACCTC CTCTTATTCTGTTGCCCAGTCTGGAGTGTAGTGGTACAATCATGGCTCACTGTAGCCTCCACCTC T C TRIM26 Ensembl:ENSG00000234127 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1181133340 Functional Loss SNV dbSNP153 33..33 33 - - - 19387 RMVar_ID_19387 Human_SNP_ID_271639194 A-to-I Human chr6 - 30201722 30201722 30201722 CTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGTGCATGCTACCACACCTGGATAATTTTT CTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTGCAGGTGCATGCTACCACACCTGGATAATTTTT T C TRIM26 Ensembl:ENSG00000234127 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1036896221 Functional Loss SNV dbSNP153 33..33 33 - - - 19388 RMVar_ID_19388 Human_SNP_ID_271639591 A-to-I Human chr6 - 30203544 30203544 30203544 GGATGTGGTGGTGGGCACCTGTAATCCCAGCTACTAGGGAGGCTGAGGCAGGAGAATCGCTTGAA GGATGTGGTGGTGGGCACCTGTAATCCCAGCTGCTAGGGAGGCTGAGGCAGGAGAATCGCTTGAA T C TRIM26 Ensembl:ENSG00000234127 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs996114882 Functional Loss SNV dbSNP153 33..33 33 - - - 19389 RMVar_ID_19389 Human_SNP_ID_271639593 A-to-I Human chr6 - 30203548 30203547 30203548 AGCCGGATGTGGTGGTGGGCACCTGTAATCCCAGCTACTAGGGAGGCTGAGGCAGGAGAATCGCT AGCCGGATGTGGTGGTGGGCACCTGTAATCCC_GCTACTAGGGAGGCTGAGGCAGGAGAATCGCT CT C TRIM26 Ensembl:ENSG00000234127 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1371749508 Functional Loss DEL dbSNP153 33..33 33 - - - 19390 RMVar_ID_19390 Human_SNP_ID_271641194 A-to-I Human chr6 - 30211387 30211387 30211387 GGACCCCCCCAGGATCAGAATAGAAAAGACACAGAGAATGGGAAATTGGTTTGAGAAGACAAAAA GGACCCCCCCAGGATCAGAATAGAAAAGACACGGAGAATGGGAAATTGGTTTGAGAAGACAAAAA T C TRIM26 Ensembl:ENSG00000234127 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs3130385 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_1661,GWAS_ID_1662,GWAS_ID_1663,GWAS_ID_1664,GWAS_ID_1665,GWAS_ID_1666,GWAS_ID_1667,GWAS_ID_1668,GWAS_ID_1669,GWAS_ID_1670,GWAS_ID_1671,GWAS_ID_1672,GWAS_ID_1673,GWAS_ID_1674 19391 RMVar_ID_19391 Human_SNP_ID_271651707 A-to-I Human chr6 + 30260470 30260470 30260470 TGAACGAGGACCTGCACTCCTGGACCGCCGCGAACACAGCGGCTCAGATCTCCCAGCACAAGTGG TGAACGAGGACCTGCACTCCTGGACCGCCGCGTACACAGCGGCTCAGATCTCCCAGCACAAGTGG A T HLA-L Ensembl:ENSG00000243753 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1438166250 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_950533,Human_RBP_ID_18539667 Human_Splice_Rec_748392,Human_Splice_Rec_748404 19392 RMVar_ID_19392 Human_SNP_ID_271652060 A-to-I Human chr6 - 30261597 30261597 30261597 GCAACGATGCCCACGATGGGGATGGTGGGCTGAGAAGACGGCTCTGGGAAAGGAGAGGGAGGTGA GCAACGATGCCCACGATGGGGATGGTGGGCTGGGAAGACGGCTCTGGGAAAGGAGAGGGAGGTGA T C HCG17 Ensembl:ENSG00000270604 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170865126 Functional Loss SNV dbSNP153 33..33 33 - - - 19393 RMVar_ID_19393 Human_SNP_ID_271661431 A-to-I Human chr6 - 30308885 30308885 30308885 AAAAAAAAAAAAAAAGCCAGGCCAGGTGCGGTAGCTCATGCCTGTAATCCCAGCACTTTGGGAGG AAAAAAAAAAAAAAAGCCAGGCCAGGTGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGG T C HCG17,HCG18 Ensembl:ENSG00000270604,Ensembl:ENSG00000231074 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs955510274 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67769 19394 RMVar_ID_19394 Human_SNP_ID_271661899 A-to-I Human chr6 - 30310921 30310921 30310921 GTAATTCTAATGCCTCAGCCTCCCAAGTAGCTAGGACTATAGGCATGCACCAACATGCCCAGCTA GTAATTCTAATGCCTCAGCCTCCCAAGTAGCTCGGACTATAGGCATGCACCAACATGCCCAGCTA T G HCG17,HCG18 Ensembl:ENSG00000270604,Ensembl:ENSG00000231074 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs528341092 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67769 19395 RMVar_ID_19395 Human_SNP_ID_271663389 A-to-I Human chr6 - 30318665 30318665 30318665 CCCACCTTGGCCTCCCAGAGCCCTGGGATTACAGGCATGAGCCACTACGCCTGGACTGGAGGGGT CCCACCTTGGCCTCCCAGAGCCCTGGGATTACGGGCATGAGCCACTACGCCTGGACTGGAGGGGT T C HCG17,HCG18 Ensembl:ENSG00000270604,Ensembl:ENSG00000231074 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1362156477 Functional Loss SNV dbSNP153 33..33 33 - - - 19396 RMVar_ID_19396 Human_SNP_ID_271663408 A-to-I Human chr6 - 30318744 30318744 30318744 TTTTTTTTTTTCTGTTGTAGAGACAGAGTCTTACTGTGTTGCCCAGGCCGGTCTCAAACTCCTGG TTTTTTTTTTTCTGTTGTAGAGACAGAGTCTTTCTGTGTTGCCCAGGCCGGTCTCAAACTCCTGG T A HCG17,HCG18 Ensembl:ENSG00000270604,Ensembl:ENSG00000231074 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1268653465 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25994839 19397 RMVar_ID_19397 Human_SNP_ID_271698693 A-to-I Human chr6 + 30470098 30470097 30470098 AATACCTGTTGTGGTACAGTTACAAGGTACACAAGTTGATGATGTTAAGGCACTAAAAGCAGACA AATACCTGTTGTGGTACAGTTACAAGGTACAC_AGTTGATGATGTTAAGGCACTAAAAGCAGACA CA C SUCLA2P1 Ensembl:ENSG00000224936 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170592339 Functional Loss DEL dbSNP153 33..33 33 - - - 19398 RMVar_ID_19398 Human_SNP_ID_271702344 A-to-I Human chr6 + 30485911 30485911 30485911 ATAATAATCCTTCCTTCCTGAGTCAGACGGGCATGGAGACGCTTCTGGAAGGAACACCGCAATGG ATAATAATCCTTCCTTCCTGAGTCAGACGGGCGTGGAGACGCTTCTGGAAGGAACACCGCAATGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879098832 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4910906 19399 RMVar_ID_19399 Human_SNP_ID_271702350 A-to-I Human chr6 + 30485934 30485934 30485934 CAGACGGGCATGGAGACGCTTCTGGAAGGAACACCGCAATGGCTGCGCAGGGACAGCCCCAGGTC CAGACGGGCATGGAGACGCTTCTGGAAGGAACGCCGCAATGGCTGCGCAGGGACAGCCCCAGGTC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878885739 Functional Loss SNV dbSNP153 33..33 33 - - - 19400 RMVar_ID_19400 Human_SNP_ID_271702353 A-to-I Human chr6 + 30485939 30485939 30485939 GGGCATGGAGACGCTTCTGGAAGGAACACCGCAATGGCTGCGCAGGGACAGCCCCAGGTCCAGTT GGGCATGGAGACGCTTCTGGAAGGAACACCGCGATGGCTGCGCAGGGACAGCCCCAGGTCCAGTT A G lnc-HLA-E-5,lnc-HLA-E-5:2 RNACentral:URS00009B7853,RNACentral:URS00009BA13C lincRNA,lincRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879208149 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4910908 19401 RMVar_ID_19401 Human_SNP_ID_271704028 A-to-I Human chr6 + 30492088 30492088 30492088 CTCCCAAAGTGCTGGGATTACAGTCGTGAGCCACCGCACCCAGCCGCACCTACTCTTTTGTAAAG CTCCCAAAGTGCTGGGATTACAGTCGTGAGCCCCCGCACCCAGCCGCACCTACTCTTTTGTAAAG A C HLA-E Ensembl:ENSG00000204592 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs936430318 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_791427 19402 RMVar_ID_19402 Human_SNP_ID_271704029 A-to-I Human chr6 + 30492088 30492088 30492088 CTCCCAAAGTGCTGGGATTACAGTCGTGAGCCACCGCACCCAGCCGCACCTACTCTTTTGTAAAG CTCCCAAAGTGCTGGGATTACAGTCGTGAGCCGCCGCACCCAGCCGCACCTACTCTTTTGTAAAG A G HLA-E Ensembl:ENSG00000204592 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs936430318 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_791427 19403 RMVar_ID_19403 Human_SNP_ID_271717603 A-to-I Human chr6 - 30552011 30552011 30552011 AAAGATAAAGAAAACTAGCCAAGTGTGGTGGTATGTGCCTGTAGTCTCTGCTACTTCAGAGGCTG AAAGATAAAGAAAACTAGCCAAGTGTGGTGGTGTGTGCCTGTAGTCTCTGCTACTTCAGAGGCTG T C GNL1 Ensembl:ENSG00000204590 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285352000 Functional Loss SNV dbSNP153 33..33 33 - - - 19404 RMVar_ID_19404 Human_SNP_ID_271719079 A-to-I Human chr6 - 30557060 30557060 30557060 ACTCTTTTCTTCCCTCGCTGGAAAACACCACAACCAGCTCCTCAGAGTGTGTCACAGAGTCAACA ACTCTTTTCTTCCCTCGCTGGAAAACACCACAGCCAGCTCCTCAGAGTGTGTCACAGAGTCAACA T C GNL1 Ensembl:ENSG00000204590 Protein coding 5'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs901341501 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_660726,Human_RBP_ID_3805708,Human_RBP_ID_22310553,Human_RBP_ID_25995022 19405 RMVar_ID_19405 Human_SNP_ID_271721253 A-to-I Human chr6 - 30566328 30566328 30566328 TTATTTATAAATGCCCACCACCACGCCTCGCTAGTTGTTGTTATTTTAGTAGAGACAGGGTTTCA TTATTTATAAATGCCCACCACCACGCCTCGCTGGTTGTTGTTATTTTAGTAGAGACAGGGTTTCA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs922981898 Functional Loss SNV dbSNP153 33..33 33 - - - 19406 RMVar_ID_19406 Human_SNP_ID_271721544 A-to-I Human chr6 - 30567548 30567548 30567548 AAGGATCCTCCCACCTCAGCCTCCAACTAGCTAGGACTACAGGCACACGCCACCAGGCCTGGGTA AAGGATCCTCCCACCTCAGCCTCCAACTAGCTGGGACTACAGGCACACGCCACCAGGCCTGGGTA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs865777245 Functional Loss SNV dbSNP153 33..33 33 - - - 19407 RMVar_ID_19407 Human_SNP_ID_271723124 A-to-I Human chr6 + 30574338 30574338 30574338 TTTTTTGTTTTCTGTAGAGATGAGGTCTTGCTATGTTGCCCAGGCTAATCTTGAACCTCTGGCCT TTTTTTGTTTTCTGTAGAGATGAGGTCTTGCTGTGTTGCCCAGGCTAATCTTGAACCTCTGGCCT A G ABCF1 Ensembl:ENSG00000204574 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1265964516 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15782731 19408 RMVar_ID_19408 Human_SNP_ID_271723127 A-to-I Human chr6 + 30574352 30574352 30574352 TAGAGATGAGGTCTTGCTATGTTGCCCAGGCTAATCTTGAACCTCTGGCCTCAACCAGTCCTCCC TAGAGATGAGGTCTTGCTATGTTGCCCAGGCTGATCTTGAACCTCTGGCCTCAACCAGTCCTCCC A G ABCF1 Ensembl:ENSG00000204574 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1354983196 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15782734 19409 RMVar_ID_19409 Human_SNP_ID_271723461 A-to-I Human chr6 + 30575868 30575868 30575868 GAGGCAGGAGAATTGCTTGAGGCCAGAGGTTCAGGATTAGCCTGAGCAACATAGTGAGACCTCCT GAGGCAGGAGAATTGCTTGAGGCCAGAGGTTCGGGATTAGCCTGAGCAACATAGTGAGACCTCCT A G ABCF1 Ensembl:ENSG00000204574 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs527367314 Functional Loss SNV dbSNP153 33..33 33 - - - 19410 RMVar_ID_19410 Human_SNP_ID_271726524 A-to-I Human chr6 + 30586997 30586997 30586997 TATAGAACGATTAAAAATTGCATAAACGGGCCAGGCACAGTAGCTCACTCCTATAATCCCAGCAG TATAGAACGATTAAAAATTGCATAAACGGGCCGGGCACAGTAGCTCACTCCTATAATCCCAGCAG A G ABCF1 Ensembl:ENSG00000204574 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904252482 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15782929 RMVar_hsa_circ_66645,RMVar_hsa_circ_109665,RMVar_hsa_circ_237810 19411 RMVar_ID_19411 Human_SNP_ID_271726629 A-to-I Human chr6 + 30587328 30587328 30587328 ATCCCAACTCTTTGGGGGAGGCTGAGGCAGGCAGATCACTTGAGCTTAGGAGTTAAAAACCAGCC ATCCCAACTCTTTGGGGGAGGCTGAGGCAGGCGGATCACTTGAGCTTAGGAGTTAAAAACCAGCC A G ABCF1 Ensembl:ENSG00000204574 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1013316183 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66645,RMVar_hsa_circ_109665,RMVar_hsa_circ_237810 19412 RMVar_ID_19412 Human_SNP_ID_271726642 A-to-I Human chr6 + 30587395 30587395 30587395 AGCCCAGTGTGGTGGCTCACACCTGTAATCCCAACACTTTGGGAAGCCGAGGTGGGAGATCACCT AGCCCAGTGTGGTGGCTCACACCTGTAATCCCGACACTTTGGGAAGCCGAGGTGGGAGATCACCT A G ABCF1 Ensembl:ENSG00000204574 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1343356937 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15782932 RMVar_hsa_circ_66645,RMVar_hsa_circ_109665,RMVar_hsa_circ_237810 19413 RMVar_ID_19413 Human_SNP_ID_271726644 A-to-I Human chr6 + 30587406 30587406 30587406 GTGGCTCACACCTGTAATCCCAACACTTTGGGAAGCCGAGGTGGGAGATCACCTGAGGTCAGGAG GTGGCTCACACCTGTAATCCCAACACTTTGGGCAGCCGAGGTGGGAGATCACCTGAGGTCAGGAG A C ABCF1 Ensembl:ENSG00000204574 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1211045761 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15782932 RMVar_hsa_circ_66645,RMVar_hsa_circ_109665,RMVar_hsa_circ_237810 19414 RMVar_ID_19414 Human_SNP_ID_271726701 A-to-I Human chr6 + 30587678 30587678 30587678 ACAGACCAGCCTGAGCAACATGGTGAAATCCCATCTCTACTAAAAATACAAAAATTAGCTGGGTA ACAGACCAGCCTGAGCAACATGGTGAAATCCCGTCTCTACTAAAAATACAAAAATTAGCTGGGTA A G ABCF1 Ensembl:ENSG00000204574 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs902145150 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66645,RMVar_hsa_circ_109665,RMVar_hsa_circ_237810 19415 RMVar_ID_19415 Human_SNP_ID_271726712 A-to-I Human chr6 + 30587734 30587734 30587734 AGCTGGGTATGTTGGTGCACGACTGTAGTCCCAGCTACTCGGGAGGCTGAGGTAGGAGAATTGCT AGCTGGGTATGTTGGTGCACGACTGTAGTCCCCGCTACTCGGGAGGCTGAGGTAGGAGAATTGCT A C ABCF1 Ensembl:ENSG00000204574 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1028468402 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66645,RMVar_hsa_circ_109665,RMVar_hsa_circ_237810 19416 RMVar_ID_19416 Human_SNP_ID_271726719 A-to-I Human chr6 + 30587774 30587774 30587774 GGGAGGCTGAGGTAGGAGAATTGCTTGAGTCCAGGGGGCAGAGGTTCCAGTTAGCCGAGGTCGTG GGGAGGCTGAGGTAGGAGAATTGCTTGAGTCCGGGGGGCAGAGGTTCCAGTTAGCCGAGGTCGTG A G ABCF1 Ensembl:ENSG00000204574 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1016085740 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17576271 RMVar_hsa_circ_66645,RMVar_hsa_circ_109665,RMVar_hsa_circ_237810 19417 RMVar_ID_19417 Human_SNP_ID_271727709 A-to-I Human chr6 + 30591576 30591576 30591576 TTCCTTTTTTTTTTTTTTTTTTTTTTTGACAGAATCTTGCCCTTTCACTCAGGCTGGAGTGCAGT TTCCTTTTTTTTTTTTTTTTTTTTTTTGACAGGATCTTGCCCTTTCACTCAGGCTGGAGTGCAGT A G ABCF1 Ensembl:ENSG00000204574 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569791101 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3002732,Human_RBP_ID_15782986,Human_RBP_ID_22310611,Human_RBP_ID_27095357 19418 RMVar_ID_19418 Human_SNP_ID_271727782 A-to-I Human chr6 + 30591901 30591901 30591901 CTGAGACAGGGTCTTGCTGTGTTGCCCAGGCTAGAGTGCACTGTACCCTCAACCTCCTGGGCTCA CTGAGACAGGGTCTTGCTGTGTTGCCCAGGCTGGAGTGCACTGTACCCTCAACCTCCTGGGCTCA A G ABCF1 Ensembl:ENSG00000204574 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1397112851 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15782988 19419 RMVar_ID_19419 Human_SNP_ID_271727792 A-to-I Human chr6 + 30591946 30591946 30591946 CCCTCAACCTCCTGGGCTCAAGCAATCCTTCCACCTCAGCCTCCTGAGTAGCTGGGACTACAGGC CCCTCAACCTCCTGGGCTCAAGCAATCCTTCCCCCTCAGCCTCCTGAGTAGCTGGGACTACAGGC A C ABCF1 Ensembl:ENSG00000204574 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1218979457 Functional Loss SNV dbSNP153 33..33 33 - - - 19420 RMVar_ID_19420 Human_SNP_ID_271727811 A-to-I Human chr6 + 30592021 30592021 30592021 ACACTCAACTAATTTTTTTTTTTTTAATTTTTAGTAGAGACAGTGTCTTGCTATGTTGCTTAAGG ACACTCAACTAATTTTTTTTTTTTTAATTTTTGGTAGAGACAGTGTCTTGCTATGTTGCTTAAGG A G ABCF1 Ensembl:ENSG00000204574 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1172595974 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7591076,Human_RBP_ID_27095361 19421 RMVar_ID_19421 Human_SNP_ID_271727812 A-to-I Human chr6 + 30592021 30592021 30592021 ACACTCAACTAATTTTTTTTTTTTTAATTTTTAGTAGAGACAGTGTCTTGCTATGTTGCTTAAGG ACACTCAACTAATTTTTTTTTTTTTAATTTTTTGTAGAGACAGTGTCTTGCTATGTTGCTTAAGG A T ABCF1 Ensembl:ENSG00000204574 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1172595974 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7591076,Human_RBP_ID_27095361 19422 RMVar_ID_19422 Human_SNP_ID_271728090 A-to-I Human chr6 + 30593281 30593281 30593281 AGGTTGCGCCACTGCACTCCAGCCTGAGCAACAGAGCGAGACTCTGTCTCAAACAAAAACCAAAA AGGTTGCGCCACTGCACTCCAGCCTGAGCAACTGAGCGAGACTCTGTCTCAAACAAAAACCAAAA A T ABCF1 Ensembl:ENSG00000204574 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1346541470 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7591094 19423 RMVar_ID_19423 Human_SNP_ID_271728644 A-to-I Human chr6 + 30595367 30595367 30595367 AAAATTAGCCAGGAGTAGTGGCACGCATTTGTAATCCCAGCTACTCAGGAAGCTGAGGCAGGAGA AAAATTAGCCAGGAGTAGTGGCACGCATTTGTCATCCCAGCTACTCAGGAAGCTGAGGCAGGAGA A C ABCF1 Ensembl:ENSG00000204574 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1327945408 Functional Loss SNV dbSNP153 33..33 33 - - - 19424 RMVar_ID_19424 Human_SNP_ID_271736815 A-to-I Human chr6 + 30622407 30622407 30622407 AGATGGTGAAACCGCATCTCTACTAAAGATACAAAATAATTAGCCAGGTGTGGTGGCAGGCGCCT AGATGGTGAAACCGCATCTCTACTAAAGATACCAAATAATTAGCCAGGTGTGGTGGCAGGCGCCT A C MRPS18B Ensembl:ENSG00000204568 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1236870428 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25995374 RMVar_hsa_circ_96075,RMVar_hsa_circ_237813 19425 RMVar_ID_19425 Human_SNP_ID_271737105 A-to-I Human chr6 + 30623289 30623289 30623289 AACCCAGGAGGCACAGGTTGTGGTGAGCCAACATTGCGCCATTGCACTCCAGCCTGGGCATCAAG AACCCAGGAGGCACAGGTTGTGGTGAGCCAACGTTGCGCCATTGCACTCCAGCCTGGGCATCAAG A G MRPS18B Ensembl:ENSG00000204568 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1218865495 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96075,RMVar_hsa_circ_237813 19426 RMVar_ID_19426 Human_SNP_ID_271739620 A-to-I Human chr6 + 30632869 30632869 30632869 TGAGGCAGGGGAATTGCTTGAATCAGGGAGGTAGAGGTTGCAGTGAGCTGAGATTGTGCCACTGC TGAGGCAGGGGAATTGCTTGAATCAGGGAGGTGGAGGTTGCAGTGAGCTGAGATTGTGCCACTGC A G ATAT1 Ensembl:ENSG00000137343 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348393031 Functional Loss SNV dbSNP153 33..33 33 - - - 19427 RMVar_ID_19427 Human_SNP_ID_271742718 A-to-I Human chr6 + 30645399 30645399 30645399 CACCGTGCCCAGCTAGTTTGTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGTTGG CACCGTGCCCAGCTAGTTTGTGTATTTTTAGTGGAGACAGGGTTTCACCATGTTGGCCAGGTTGG A G ATAT1 Ensembl:ENSG00000137343 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1453693407 Functional Loss SNV dbSNP153 33..33 33 - - - 19428 RMVar_ID_19428 Human_SNP_ID_271746418 A-to-I Human chr6 - 30658377 30658377 30658377 ACCACGCCTGGCCAATTTTTTGTATTTTTAGTAGAGATGAGGTTTCGCTATTTTGGCCAGGTTGG ACCACGCCTGGCCAATTTTTTGTATTTTTAGTGGAGATGAGGTTTCGCTATTTTGGCCAGGTTGG T C DHX16 Ensembl:ENSG00000204560 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs373298516 Functional Loss SNV dbSNP153 33..33 33 - - - 19429 RMVar_ID_19429 Human_SNP_ID_271746604 A-to-I Human chr6 - 30659114 30659114 30659114 CGGAGGCTGAGGTGGGCGGATCACTTGAGGTCAGTAGTTCGAAACCAGGCTGCCTAACGTGGTGA CGGAGGCTGAGGTGGGCGGATCACTTGAGGTCTGTAGTTCGAAACCAGGCTGCCTAACGTGGTGA T A DHX16 Ensembl:ENSG00000204560 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1561976104 Functional Loss SNV dbSNP153 33..33 33 - - - 19430 RMVar_ID_19430 Human_SNP_ID_271747076 A-to-I Human chr6 - 30660770 30660770 30660770 TCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCGTCTACCACCACATCTG TCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTTGCTGGGACTACAGGCGTCTACCACCACATCTG T A DHX16 Ensembl:ENSG00000204560 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs911127837 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_172834 19431 RMVar_ID_19431 Human_SNP_ID_271747077 A-to-I Human chr6 - 30660770 30660770 30660770 TCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCGTCTACCACCACATCTG TCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTCGCTGGGACTACAGGCGTCTACCACCACATCTG T G DHX16 Ensembl:ENSG00000204560 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs911127837 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_172834 19432 RMVar_ID_19432 Human_SNP_ID_271747125 A-to-I Human chr6 - 30660960 30660960 30660960 CCAGGAGGCGGAGCTTGCAGTGAGCTGAGATCATGCCACTACACTCCAGCCTGCAACAGAGCAAG CCAGGAGGCGGAGCTTGCAGTGAGCTGAGATCGTGCCACTACACTCCAGCCTGCAACAGAGCAAG T C DHX16 Ensembl:ENSG00000204560 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs576345384 Functional Loss SNV dbSNP153 33..33 33 - - - 19433 RMVar_ID_19433 Human_SNP_ID_271759633 A-to-I Human chr6 - 30709243 30709242 30709243 GGAGACCAATGTGGGTGGATCACTTGAGTCTAAGAGTTCAAGACCAAACCCCATCTCTACAACAA GGAGACCAATGTGGGTGGATCACTTGAGTCTA_GAGTTCAAGACCAAACCCCATCTCTACAACAA CT C MDC1 Ensembl:ENSG00000137337 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355852436 Functional Loss DEL dbSNP153 33..33 33 - - - 19434 RMVar_ID_19434 Human_SNP_ID_271760016 A-to-I Human chr6 - 30711157 30711157 30711157 TTGGCCAGGCTGGTCACAAACTCCCGACCTCAAGTGATCCGCCTGCCTCGGCCTCCCAAAATGCT TTGGCCAGGCTGGTCACAAACTCCCGACCTCAGGTGATCCGCCTGCCTCGGCCTCCCAAAATGCT T C MDC1 Ensembl:ENSG00000137337 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025257532 Functional Loss SNV dbSNP153 33..33 33 - - - 19435 RMVar_ID_19435 Human_SNP_ID_271765918 A-to-I Human chr6 - 30733995 30733995 30733995 TGTTGTCCAATACAGTGGCATAAACAAGGCTCACTGTAACCTCAACCTCCCAGGCTCAAGTGATT TGTTGTCCAATACAGTGGCATAAACAAGGCTCTCTGTAACCTCAACCTCCCAGGCTCAAGTGATT T A FLOT1 Ensembl:ENSG00000137312 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1458953601 Functional Loss SNV dbSNP153 33..33 33 - - - 19436 RMVar_ID_19436 Human_SNP_ID_271766241 A-to-I Human chr6 - 30735429 30735429 30735429 TTTTTTTTTTTTTAGTAGAGAGGGGTTTCACCATGTCGGCCAGGCTGGTCTCGAACTGCTAGCCT TTTTTTTTTTTTTAGTAGAGAGGGGTTTCACCGTGTCGGCCAGGCTGGTCTCGAACTGCTAGCCT T C FLOT1 Ensembl:ENSG00000137312 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006109676 Functional Loss SNV dbSNP153 33..33 33 - - - 19437 RMVar_ID_19437 Human_SNP_ID_271766379 A-to-I Human chr6 - 30736069 30736069 30736069 TTTTGTATGTTTTGTAGAGACGGAATTTCACCATGTTGCCCAGGCTGGTCTCAAACTCCTGGGCT TTTTGTATGTTTTGTAGAGACGGAATTTCACCGTGTTGCCCAGGCTGGTCTCAAACTCCTGGGCT T C FLOT1 Ensembl:ENSG00000137312 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs900496385 Functional Loss SNV dbSNP153 33..33 33 - - - 19438 RMVar_ID_19438 Human_SNP_ID_271766385 A-to-I Human chr6 - 30736095 30736095 30736095 AACATATGCCACCACGCCTGGCTAATTTTTGTATGTTTTGTAGAGACGGAATTTCACCATGTTGC AACATATGCCACCACGCCTGGCTAATTTTTGTTTGTTTTGTAGAGACGGAATTTCACCATGTTGC T A FLOT1 Ensembl:ENSG00000137312 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1467913960 Functional Loss SNV dbSNP153 33..33 33 - - - 19439 RMVar_ID_19439 Human_SNP_ID_271864932 A-to-I Human chr6 + 31135016 31135016 31135016 TTTCTTAAATTTTCTGTAGAAACAGTTTTGCCATGTTGCCTAGGCTGGTCTCAAACTCCTGGCCA TTTCTTAAATTTTCTGTAGAAACAGTTTTGCCGTGTTGCCTAGGCTGGTCTCAAACTCCTGGCCA A G PSORS1C1 Ensembl:ENSG00000204540 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031889011 Functional Loss SNV dbSNP153 33..33 33 - - - 19440 RMVar_ID_19440 Human_SNP_ID_271865014 A-to-I Human chr6 + 31135427 31135427 31135427 TTTTTAGTAGAGACAGAGTTTCACCATTGTCCAGGCTGGTCTTGAATTGCTGACCTCAAGTGATC TTTTTAGTAGAGACAGAGTTTCACCATTGTCCGGGCTGGTCTTGAATTGCTGACCTCAAGTGATC A G PSORS1C1 Ensembl:ENSG00000204540 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1208745583 Functional Loss SNV dbSNP153 33..33 33 - - - 19441 RMVar_ID_19441 Human_SNP_ID_271865017 A-to-I Human chr6 + 31135452 31135452 31135452 ATTGTCCAGGCTGGTCTTGAATTGCTGACCTCAAGTGATCTGCCTACCTCAGCCTCCCAAATGCT ATTGTCCAGGCTGGTCTTGAATTGCTGACCTCGAGTGATCTGCCTACCTCAGCCTCCCAAATGCT A G PSORS1C1 Ensembl:ENSG00000204540 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs966918726 Functional Loss SNV dbSNP153 33..33 33 - - - 19442 RMVar_ID_19442 Human_SNP_ID_271867526 A-to-I Human chr6 - 31144355 31144355 31144355 CCCTGTCTCGACTAAAAATACAAAAATTAGCTAGGCCTGGTGGTGGGCACCTGTACCCCAAGCTT CCCTGTCTCGACTAAAAATACAAAAATTAGCTCGGCCTGGTGGTGGGCACCTGTACCCCAAGCTT T G CCHCR1 Ensembl:ENSG00000204536 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs574605540 Functional Loss SNV dbSNP153 33..33 33 - - - 19443 RMVar_ID_19443 Human_SNP_ID_271868907 A-to-I Human chr6 - 31149472 31149472 31149472 GATCCCATCACTGCACTCTAGCCTGGGTGACAAAGCGAGATCTTTTCTCAAAAAAAAAGAAAGTA GATCCCATCACTGCACTCTAGCCTGGGTGACAGAGCGAGATCTTTTCTCAAAAAAAAAGAAAGTA T C CCHCR1 Ensembl:ENSG00000204536 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs901622315 Functional Loss SNV dbSNP153 33..33 33 - - - 19444 RMVar_ID_19444 Human_SNP_ID_271868932 A-to-I Human chr6 - 31149597 31149597 31149597 TCTACTAAAAATACAAAAAATTAGCCGGTCATAGTGGCTCATTCCTGTAGTCCCAGCTACTCTGG TCTACTAAAAATACAAAAAATTAGCCGGTCATGGTGGCTCATTCCTGTAGTCCCAGCTACTCTGG T C CCHCR1 Ensembl:ENSG00000204536 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1301119396 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23314628 Human_Splice_Rec_751468 19445 RMVar_ID_19445 Human_SNP_ID_271873562 A-to-I Human chr6 - 31167536 31167536 31167536 GCCCAGCTAATTTTTGTATTTTTAGTAGAGACAGAGTCTCACTATGTTGACCAGGCTAGTCTTGA GCCCAGCTAATTTTTGTATTTTTAGTAGAGACGGAGTCTCACTATGTTGACCAGGCTAGTCTTGA T C POU5F1 Ensembl:ENSG00000204531 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs374544416 Functional Loss SNV dbSNP153 33..33 33 - - - 19446 RMVar_ID_19446 Human_SNP_ID_271873567 A-to-I Human chr6 - 31167560 31167560 31167560 GGGATTATAGGGGAGCGCCATGATGCCCAGCTAATTTTTGTATTTTTAGTAGAGACAGAGTCTCA GGGATTATAGGGGAGCGCCATGATGCCCAGCTGATTTTTGTATTTTTAGTAGAGACAGAGTCTCA T C POU5F1 Ensembl:ENSG00000204531 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037266508 Functional Loss SNV dbSNP153 33..33 33 - - - 19447 RMVar_ID_19447 Human_SNP_ID_271875261 A-to-I Human chr6 - 31174728 31174728 31174728 CCTCAGCCTCCTAAAGTGCTGGGATTATAGGCATGAGCCACCGCTCCCGGCCTCCTCCTATATCT CCTCAGCCTCCTAAAGTGCTGGGATTATAGGCGTGAGCCACCGCTCCCGGCCTCCTCCTATATCT T C POU5F1,PSORS1C3 Ensembl:ENSG00000204531,Ensembl:ENSG00000204528 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1055628544 Functional Loss SNV dbSNP153 33..33 33 - - - 19448 RMVar_ID_19448 Human_SNP_ID_271875662 A-to-I Human chr6 - 31176696 31176696 31176696 GTGATCCACCTGCCTGGGCCTCCCAAAGTGCTAGGATTACAGGCGTGAGCCACCGCACCCGGCCA GTGATCCACCTGCCTGGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCACCCGGCCA T C POU5F1,PSORS1C3 Ensembl:ENSG00000204531,Ensembl:ENSG00000204528 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1412303584 Functional Loss SNV dbSNP153 33..33 33 - - - 19449 RMVar_ID_19449 Human_SNP_ID_271876443 A-to-I Human chr6 - 31180177 31180177 31180177 TGGCCGTAGGAGGTCCTTATGCCTGTAATCCCAGGACTTTGGGAGGCCGAGCTGGGCGGAGGATT TGGCCGTAGGAGGTCCTTATGCCTGTAATCCCGGGACTTTGGGAGGCCGAGCTGGGCGGAGGATT T C POU5F1 Ensembl:ENSG00000204531 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1286343188 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17576278 19450 RMVar_ID_19450 Human_SNP_ID_271876856 A-to-I Human chr6 - 31181509 31181505 31181509 AAATTCTCTCTCTTTTTTTGAGACGGAGTCTCACTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCT AAATTCTCTCTCTTTTTTTGAGACGGAGTCTC____TGTCGCCCAGGCTGGAGTGCAGTGGCGCT AGAGT A PSORS1C3,PSORS1C3:2,PSORS1C3:3,PSORS1C3:4,PSORS1C3:5,PSORS1C3:6,PSORS1C3:7,PSORS1C3:8,PSORS1C3:9,PSORS1C3:10,PSORS1C3:11,PSORS1C3:12,PSORS1C3:13,PSORS1C3:14,PSORS1C3:15,PSORS1C3:16,PSORS1C3:17 RNACentral:URS00008F95C6,RNACentral:URS0000CCDFFA,RNACentral:URS00008E7EE6,RNACentral:URS00008FEAE5,RNACentral:URS00008F95B7,RNACentral:URS00008E3EDF,RNACentral:URS00008EE078,RNACentral:URS00008C19ED,RNACentral:URS00008FE3A4,RNACentral:URS00008F8E8F,RNACentral:URS00008EE658,RNACentral:URS00008FCA9D,RNACentral:URS00008406BA,RNACentral:URS00008F066B,RNACentral:URS00008F969C,RNACentral:URS000083C8B0,RNACentral:URS00008EFDB7 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 GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1398958913 Functional Loss DEL dbSNP153 33..36 33 - - - 19451 RMVar_ID_19451 Human_SNP_ID_271876857 A-to-I Human chr6 - 31181509 31181509 31181509 AAATTCTCTCTCTTTTTTTGAGACGGAGTCTCACTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCT AAATTCTCTCTCTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCT T C PSORS1C3,PSORS1C3:2,PSORS1C3:3,PSORS1C3:4,PSORS1C3:5,PSORS1C3:6,PSORS1C3:7,PSORS1C3:8,PSORS1C3:9,PSORS1C3:10,PSORS1C3:11,PSORS1C3:12,PSORS1C3:13,PSORS1C3:14,PSORS1C3:15,PSORS1C3:16,PSORS1C3:17 RNACentral:URS00008F95C6,RNACentral:URS0000CCDFFA,RNACentral:URS00008E7EE6,RNACentral:URS00008FEAE5,RNACentral:URS00008F95B7,RNACentral:URS00008E3EDF,RNACentral:URS00008EE078,RNACentral:URS00008C19ED,RNACentral:URS00008FE3A4,RNACentral:URS00008F8E8F,RNACentral:URS00008EE658,RNACentral:URS00008FCA9D,RNACentral:URS00008406BA,RNACentral:URS00008F066B,RNACentral:URS00008F969C,RNACentral:URS000083C8B0,RNACentral:URS00008EFDB7 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 GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1292115423 Functional Loss SNV dbSNP153 33..33 33 - - - 19452 RMVar_ID_19452 Human_SNP_ID_271881513 A-to-I Human chr6 + 31198455 31198455 31198455 TTGTTATTTATTTATGTATTTTATTTTTTTTGAGACAGTCTTGGTCTGTCACCCAGACTGGAGTG TTGTTATTTATTTATGTATTTTATTTTTTTTGCGACAGTCTTGGTCTGTCACCCAGACTGGAGTG A C HCG27 Ensembl:ENSG00000206344 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs753478538 Functional Loss SNV dbSNP153 33..33 33 - - - 19453 RMVar_ID_19453 Human_SNP_ID_271881566 A-to-I Human chr6 + 31198575 31198575 31198575 TTCCTGCCTCAGCCTCCCAAGTAGCTGCGATTACAGGCACCCCCCACCACGCCCGGCTGATTTTT TTCCTGCCTCAGCCTCCCAAGTAGCTGCGATTGCAGGCACCCCCCACCACGCCCGGCTGATTTTT A G HCG27 Ensembl:ENSG00000206344 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs3130465 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_1675,GWAS_ID_1676 19454 RMVar_ID_19454 Human_SNP_ID_271881567 A-to-I Human chr6 + 31198575 31198575 31198575 TTCCTGCCTCAGCCTCCCAAGTAGCTGCGATTACAGGCACCCCCCACCACGCCCGGCTGATTTTT TTCCTGCCTCAGCCTCCCAAGTAGCTGCGATTTCAGGCACCCCCCACCACGCCCGGCTGATTTTT A T HCG27 Ensembl:ENSG00000206344 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs3130465 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_1675,GWAS_ID_1676 19455 RMVar_ID_19455 Human_SNP_ID_271899936 A-to-I Human chr6 - 31270298 31270298 31270298 CCAGCAGGAGATGGAACCTTCCAGAAGTGGGCAGCTGTGGTGGTGCCTTCTGGACAAGAGCAGAG CCAGCAGGAGATGGAACCTTCCAGAAGTGGGCGGCTGTGGTGGTGCCTTCTGGACAAGAGCAGAG T C HLA-C,HLA-B Ensembl:ENSG00000204525,Ensembl:ENSG00000234745 Protein coding,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1323498643 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_661251,Human_RBP_ID_5617756 Human_Splice_Rec_751681,Human_Splice_Rec_751689,Human_Splice_Rec_751703,Human_Splice_Rec_751717,Human_Splice_Rec_751731,Human_Splice_Rec_751745 19456 RMVar_ID_19456 Human_SNP_ID_271903138 A-to-I Human chr6 - 31278295 31278295 31278295 TTCTTCTTTAGAAAATAATCTAAGGCAATCCTATAATGTACATTTACTTGTGGATGCTATCAGTA TTCTTCTTTAGAAAATAATCTAAGGCAATCCTTTAATGTACATTTACTTGTGGATGCTATCAGTA T A HLA-B Ensembl:ENSG00000234745 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs527244094 Functional Loss SNV dbSNP153 33..33 33 - - - 19457 RMVar_ID_19457 Human_SNP_ID_271903139 A-to-I Human chr6 - 31278295 31278295 31278295 TTCTTCTTTAGAAAATAATCTAAGGCAATCCTATAATGTACATTTACTTGTGGATGCTATCAGTA TTCTTCTTTAGAAAATAATCTAAGGCAATCCTGTAATGTACATTTACTTGTGGATGCTATCAGTA T C HLA-B Ensembl:ENSG00000234745 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs527244094 Functional Loss SNV dbSNP153 33..33 33 - - - 19458 RMVar_ID_19458 Human_SNP_ID_271922780 A-to-I Human chr6 + 31354085 31354085 31354085 ACATCCAGCCCCACCTCTCTGGAACAAGAAAGATGACTGGGGAGGAAACACAGGTCAGCATGGGA ACATCCAGCCCCACCTCTCTGGAACAAGAAAGTTGACTGGGGAGGAAACACAGGTCAGCATGGGA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs927982665 Functional Loss SNV dbSNP153 33..33 33 - - - 19459 RMVar_ID_19459 Human_SNP_ID_271936090 A-to-I Human chr6 - 31399451 31399451 31399451 TTGGCTCACTGCAAGCTCCGCCTCCCGGGTTCAGGGCATTCTGCTGCCTCAGCCTCTGGAGTAGC TTGGCTCACTGCAAGCTCCGCCTCCCGGGTTCCGGGCATTCTGCTGCCTCAGCCTCTGGAGTAGC T G MICA-AS1 RNACentral:URS0000BC4549 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1477792325 Functional Loss SNV dbSNP153 33..33 33 - - - 19460 RMVar_ID_19460 Human_SNP_ID_271940187 A-to-I Human chr6 + 31415403 31415403 31415403 GTCTCAGGCCAGGCACGGTGGCTCACGCCTGTAATCCCAACACTTTGGGAGGCCGAGGCGGGCGG GTCTCAGGCCAGGCACGGTGGCTCACGCCTGTGATCCCAACACTTTGGGAGGCCGAGGCGGGCGG A G AL645933.5 Ensembl:ENSG00000288587 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1283524724 Functional Loss SNV dbSNP153 33..33 33 - - - 19461 RMVar_ID_19461 Human_SNP_ID_271940271 A-to-I Human chr6 + 31415678 31415677 31415679 ACTCTGTCTCAAAAAAAAAAAAAAAAAAAGACAGAGTCTCACTCTGTCACCCAGGCTGCAGTTCA ACTCTGTCTCAAAAAAAAAAAAAAAAAAAGAC__AGTCTCACTCTGTCACCCAGGCTGCAGTTCA CAG C AL645933.5 Ensembl:ENSG00000288587 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005681532 Functional Loss DEL dbSNP153 33..34 33 - - - 19462 RMVar_ID_19462 Human_SNP_ID_271940290 A-to-I Human chr6 + 31415754 31415754 31415754 TCAGCTCGTTGCAGCCTCCGCCTCCCGGGTTCAAGCACTTCTCTTGCCTCAGCCTCCCGAGTAGC TCAGCTCGTTGCAGCCTCCGCCTCCCGGGTTCGAGCACTTCTCTTGCCTCAGCCTCCCGAGTAGC A G AL645933.5 Ensembl:ENSG00000288587 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs570745654 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_1677 19463 RMVar_ID_19463 Human_SNP_ID_271940324 A-to-I Human chr6 + 31415929 31415929 31415929 TGCCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAAGCATGAGCCACCATACCCGGCCTATTTTA TGCCTGCCTCAGCCTCCCAAAGTGCTGGGATTGCAAGCATGAGCCACCATACCCGGCCTATTTTA A G AL645933.5 Ensembl:ENSG00000288587 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031385180 Functional Loss SNV dbSNP153 33..33 33 - - - 19464 RMVar_ID_19464 Human_SNP_ID_271974065 A-to-I Human chr6 + 31543725 31543725 31543725 GAGACCCCATCTCTACAAAAAATTTTAAAATTAGCAAGGCATAGTGGCACTCGCCCGTAATCCCA GAGACCCCATCTCTACAAAAAATTTTAAAATTGGCAAGGCATAGTGGCACTCGCCCGTAATCCCA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991947046 Functional Loss SNV dbSNP153 33..33 33 - - - 19465 RMVar_ID_19465 Human_SNP_ID_271974066 A-to-I Human chr6 + 31543725 31543725 31543725 GAGACCCCATCTCTACAAAAAATTTTAAAATTAGCAAGGCATAGTGGCACTCGCCCGTAATCCCA GAGACCCCATCTCTACAAAAAATTTTAAAATTTGCAAGGCATAGTGGCACTCGCCCGTAATCCCA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991947046 Functional Loss SNV dbSNP153 33..33 33 - - - 19466 RMVar_ID_19466 Human_SNP_ID_271992005 A-to-I Human chr6 - 31617651 31617651 31617651 CAATGATGCGATCTCGGATCACCACAACCTCCACCTCCTGGGTTCAAGAGATTCTCCTGCCTCAG CAATGATGCGATCTCGGATCACCACAACCTCCGCCTCCTGGGTTCAAGAGATTCTCCTGCCTCAG T C lnc-BBS5-6 RNACentral:URS0000E2127A lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs759606992 Functional Loss SNV dbSNP153 33..33 33 - - - 19467 RMVar_ID_19467 Human_SNP_ID_271995823 A-to-I Human chr6 - 31628693 31628693 31628693 GGGACTACAAGCACATGCCACCACACTTGGCTAATTTTTGTATTTTTAGTAGAGACGGGTTTCAC GGGACTACAAGCACATGCCACCACACTTGGCTGATTTTTGTATTTTTAGTAGAGACGGGTTTCAC T C RF00017-4520,lnc-BBS5-6 RNACentral:URS000099C2D3,RNACentral:URS0000E2127A SRP RNA,lincRNA intron,intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs776216708 Functional Loss SNV dbSNP153 33..33 33 - - - 19468 RMVar_ID_19468 Human_SNP_ID_272004790 A-to-I Human chr6 - 31653874 31653874 31653874 GGCCAAGTCTGCAAGACCAGGCTGGGCAACATAGCAAGACCCCATCTCTATAAAAATAAAATTAG GGCCAAGTCTGCAAGACCAGGCTGGGCAACATGGCAAGACCCCATCTCTATAAAAATAAAATTAG T C RF00017-4520,lnc-BBS5-6 RNACentral:URS000099C2D3,RNACentral:URS0000E2127A SRP RNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs920759704 Functional Loss SNV dbSNP153 33..33 33 - - - 19469 RMVar_ID_19469 Human_SNP_ID_272006522 A-to-I Human chr6 - 31660475 31660475 31660475 GGAGTTTGCTGGACACTTTCATTCCACCTCCTAACAAAGAGAATTCCTATTCCTTGAGGTCCCTT GGAGTTTGCTGGACACTTTCATTCCACCTCCTGACAAAGAGAATTCCTATTCCTTGAGGTCCCTT T C C6orf47 Ensembl:ENSG00000204439 Protein coding 5'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1262064506 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4903835,Human_RBP_ID_5428412,Human_RBP_ID_5451099,Human_RBP_ID_5478040,Human_RBP_ID_5511439,Human_RBP_ID_9193523,Human_RBP_ID_18073713,Human_RBP_ID_26828220 19470 RMVar_ID_19470 Human_SNP_ID_272010236 A-to-I Human chr6 + 31672506 31672506 31672506 TCGCTCTGTCACCCAGGGTGGAGTGCAGTGGCATGATCTCTGCTCACTACAACCTCCACCTCCCG TCGCTCTGTCACCCAGGGTGGAGTGCAGTGGCGTGATCTCTGCTCACTACAACCTCCACCTCCCG A G LY6G5B,AL662899.4 Ensembl:ENSG00000240053,Ensembl:ENSG00000263020 Protein coding,Protein coding 3'UTR,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1012544362 Functional Loss SNV dbSNP153 33..33 33 - - - 19471 RMVar_ID_19471 Human_SNP_ID_272010287 A-to-I Human chr6 + 31672682 31672682 31672682 TGGTCAGGCTGGTCTCGAACTCCTGACCTCGTAATCTGCCCTCCTCGACCTCCCAAAGTGCCGGG TGGTCAGGCTGGTCTCGAACTCCTGACCTCGTGATCTGCCCTCCTCGACCTCCCAAAGTGCCGGG A G LY6G5B,AL662899.4 Ensembl:ENSG00000240053,Ensembl:ENSG00000263020 Protein coding,Protein coding 3'UTR,3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1405452133 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23195151 19472 RMVar_ID_19472 Human_SNP_ID_272010355 A-to-I Human chr6 + 31673010 31673010 31673010 CGAGGAGGCCGGGCATGGTGGCTCACGCCGGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGCGG CGAGGAGGCCGGGCATGGTGGCTCACGCCGGTGATCCCAGCACTTTGGGAGGCCGAGGTGGGCGG A G LY6G5B,AL662899.4 Ensembl:ENSG00000240053,Ensembl:ENSG00000263020 Protein coding,Protein coding 3'UTR,3'UTR GSE38233;GSE100210;GSE100210;GSE107867 cultured B-cells;HepG2 cell line;HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 24183664,29129909,29129909,30559470 RNA-Seq:(High) rs1449714437 Functional Loss SNV dbSNP153 33..33 33 - - - 19473 RMVar_ID_19473 Human_SNP_ID_272010357 A-to-I Human chr6 + 31673016 31673016 31673016 GGCCGGGCATGGTGGCTCACGCCGGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGCGGATCACT GGCCGGGCATGGTGGCTCACGCCGGTAATCCCGGCACTTTGGGAGGCCGAGGTGGGCGGATCACT A G LY6G5B,AL662899.4 Ensembl:ENSG00000240053,Ensembl:ENSG00000263020 Protein coding,Protein coding 3'UTR,3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1019192330 Functional Loss SNV dbSNP153 33..33 33 - - - 19474 RMVar_ID_19474 Human_SNP_ID_272010371 A-to-I Human chr6 + 31673046 31673046 31673046 CCAGCACTTTGGGAGGCCGAGGTGGGCGGATCACTTGAGATTGGGAGTTTGAGACCAGCCTGGCC CCAGCACTTTGGGAGGCCGAGGTGGGCGGATCCCTTGAGATTGGGAGTTTGAGACCAGCCTGGCC A C LY6G5B,AL662899.4 Ensembl:ENSG00000240053,Ensembl:ENSG00000263020 Protein coding,Protein coding 3'UTR,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1156280848 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23060432,Human_RBP_ID_25997009 19475 RMVar_ID_19475 Human_SNP_ID_272010378 A-to-I Human chr6 + 31673059 31673057 31673059 AGGCCGAGGTGGGCGGATCACTTGAGATTGGGAGTTTGAGACCAGCCTGGCCAACATGGTAAAAC AGGCCGAGGTGGGCGGATCACTTGAGATTGG__GTTTGAGACCAGCCTGGCCAACATGGTAAAAC GGA G LY6G5B,AL662899.4 Ensembl:ENSG00000240053,Ensembl:ENSG00000263020 Protein coding,Protein coding 3'UTR,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1195532632 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_23060432,Human_RBP_ID_25997009 19476 RMVar_ID_19476 Human_SNP_ID_272010386 A-to-I Human chr6 + 31673087 31673087 31673087 TGGGAGTTTGAGACCAGCCTGGCCAACATGGTAAAACCCGCTCTCTATTAAAAATAGAAAAATCA TGGGAGTTTGAGACCAGCCTGGCCAACATGGTGAAACCCGCTCTCTATTAAAAATAGAAAAATCA A G LY6G5B,AL662899.4 Ensembl:ENSG00000240053,Ensembl:ENSG00000263020 Protein coding,Protein coding 3'UTR,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1365873945 Functional Loss SNV dbSNP153 33..33 33 - - - 19477 RMVar_ID_19477 Human_SNP_ID_272010397 A-to-I Human chr6 + 31673104 31673104 31673104 CCTGGCCAACATGGTAAAACCCGCTCTCTATTAAAAATAGAAAAATCAGCTGGGTGTGGTGGCAC CCTGGCCAACATGGTAAAACCCGCTCTCTATTGAAAATAGAAAAATCAGCTGGGTGTGGTGGCAC A G LY6G5B,AL662899.4 Ensembl:ENSG00000240053,Ensembl:ENSG00000263020 Protein coding,Protein coding 3'UTR,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1448713465 Functional Loss SNV dbSNP153 33..33 33 - - - 19478 RMVar_ID_19478 Human_SNP_ID_272010398 A-to-I Human chr6 + 31673110 31673110 31673110 CAACATGGTAAAACCCGCTCTCTATTAAAAATAGAAAAATCAGCTGGGTGTGGTGGCACACCTCT CAACATGGTAAAACCCGCTCTCTATTAAAAATGGAAAAATCAGCTGGGTGTGGTGGCACACCTCT A G LY6G5B,AL662899.4 Ensembl:ENSG00000240053,Ensembl:ENSG00000263020 Protein coding,Protein coding 3'UTR,3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs11754259 Functional Loss SNV dbSNP153 33..33 33 - - - 19479 RMVar_ID_19479 Human_SNP_ID_272010399 A-to-I Human chr6 + 31673110 31673110 31673110 CAACATGGTAAAACCCGCTCTCTATTAAAAATAGAAAAATCAGCTGGGTGTGGTGGCACACCTCT CAACATGGTAAAACCCGCTCTCTATTAAAAATTGAAAAATCAGCTGGGTGTGGTGGCACACCTCT A T LY6G5B,AL662899.4 Ensembl:ENSG00000240053,Ensembl:ENSG00000263020 Protein coding,Protein coding 3'UTR,3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs11754259 Functional Loss SNV dbSNP153 33..33 33 - - - 19480 RMVar_ID_19480 Human_SNP_ID_272010401 A-to-I Human chr6 + 31673119 31673119 31673119 AAAACCCGCTCTCTATTAAAAATAGAAAAATCAGCTGGGTGTGGTGGCACACCTCTGTAATCCCA AAAACCCGCTCTCTATTAAAAATAGAAAAATCGGCTGGGTGTGGTGGCACACCTCTGTAATCCCA A G LY6G5B,AL662899.4 Ensembl:ENSG00000240053,Ensembl:ENSG00000263020 Protein coding,Protein coding 3'UTR,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1243853364 Functional Loss SNV dbSNP153 33..33 33 - - - 19481 RMVar_ID_19481 Human_SNP_ID_272010407 A-to-I Human chr6 + 31673135 31673135 31673135 TAAAAATAGAAAAATCAGCTGGGTGTGGTGGCACACCTCTGTAATCCCAGCTACTCAGGAGGCTG TAAAAATAGAAAAATCAGCTGGGTGTGGTGGCGCACCTCTGTAATCCCAGCTACTCAGGAGGCTG A G LY6G5B,AL662899.4 Ensembl:ENSG00000240053,Ensembl:ENSG00000263020 Protein coding,Protein coding 3'UTR,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1275803182 Functional Loss SNV dbSNP153 33..33 33 - - - 19482 RMVar_ID_19482 Human_SNP_ID_272010416 A-to-I Human chr6 + 31673155 31673155 31673155 GGGTGTGGTGGCACACCTCTGTAATCCCAGCTACTCAGGAGGCTGAGACAGGAGAATCACTTGAA GGGTGTGGTGGCACACCTCTGTAATCCCAGCTGCTCAGGAGGCTGAGACAGGAGAATCACTTGAA A G LY6G5B,AL662899.4 Ensembl:ENSG00000240053,Ensembl:ENSG00000263020 Protein coding,Protein coding 3'UTR,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs906451141 Functional Loss SNV dbSNP153 33..33 33 - - - 19483 RMVar_ID_19483 Human_SNP_ID_272010419 A-to-I Human chr6 + 31673159 31673159 31673159 GTGGTGGCACACCTCTGTAATCCCAGCTACTCAGGAGGCTGAGACAGGAGAATCACTTGAACCCG GTGGTGGCACACCTCTGTAATCCCAGCTACTCGGGAGGCTGAGACAGGAGAATCACTTGAACCCG A G LY6G5B,AL662899.4 Ensembl:ENSG00000240053,Ensembl:ENSG00000263020 Protein coding,Protein coding 3'UTR,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1356202189 Functional Loss SNV dbSNP153 33..33 33 - - - 19484 RMVar_ID_19484 Human_SNP_ID_272010428 A-to-I Human chr6 + 31673198 31673198 31673198 TGAGACAGGAGAATCACTTGAACCCGGGAGGCAGAGGTTGCAGTGAGCCGAGATCGCGCCACTGC TGAGACAGGAGAATCACTTGAACCCGGGAGGCGGAGGTTGCAGTGAGCCGAGATCGCGCCACTGC A G LY6G5B,AL662899.4 Ensembl:ENSG00000240053,Ensembl:ENSG00000263020 Protein coding,Protein coding 3'UTR,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1482352823 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25997011 Human_Splice_Rec_753260 19485 RMVar_ID_19485 Human_SNP_ID_272028760 A-to-I Human chr6 + 31747929 31747929 31747929 AGGAGACTAAGGCAGGAGAATCGCTTGAACCCAGGAGGTGGAGGTTGCAGTGAGCCAAGATTGTG AGGAGACTAAGGCAGGAGAATCGCTTGAACCCGGGAGGTGGAGGTTGCAGTGAGCCAAGATTGTG A G MSH5-SAPCD1,MSH5 Ensembl:ENSG00000255152,Ensembl:ENSG00000204410 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs576752675 Functional Loss SNV dbSNP153 33..33 33 - - - 19486 RMVar_ID_19486 Human_SNP_ID_272028773 A-to-I Human chr6 + 31747982 31747982 31747982 GCCAAGATTGTGCACTGCACTTCAGCCTGGGCAACAGAGTGAGACTCCGTCTCAAAAAAAAAAAA GCCAAGATTGTGCACTGCACTTCAGCCTGGGCGACAGAGTGAGACTCCGTCTCAAAAAAAAAAAA A G MSH5-SAPCD1,MSH5 Ensembl:ENSG00000255152,Ensembl:ENSG00000204410 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1045595662 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18863121 19487 RMVar_ID_19487 Human_SNP_ID_272028952 A-to-I Human chr6 + 31748622 31748622 31748622 CCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGTCACTGCGCCTGGCCGTCACTCCACTTT CCTCGGCCTCCCAAAGTGCTGGGATTACAGGCTTGAGTCACTGCGCCTGGCCGTCACTCCACTTT A T MSH5-SAPCD1,MSH5 Ensembl:ENSG00000255152,Ensembl:ENSG00000204410 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs757801058 Functional Loss SNV dbSNP153 33..33 33 - - - 19488 RMVar_ID_19488 Human_SNP_ID_272029064 A-to-I Human chr6 + 31749116 31749116 31749116 TTTTGTATTTTTAGTAGAGATGGGATTTCACCATGTTGGCCACGCTGGTCTTGAACTGCTGACCT TTTTGTATTTTTAGTAGAGATGGGATTTCACCGTGTTGGCCACGCTGGTCTTGAACTGCTGACCT A G MSH5-SAPCD1,MSH5 Ensembl:ENSG00000255152,Ensembl:ENSG00000204410 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1003964588 Functional Loss SNV dbSNP153 33..33 33 - - - 19489 RMVar_ID_19489 Human_SNP_ID_272029082 A-to-I Human chr6 + 31749194 31749194 31749194 CCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATAAGCCACTGTGCCCGGCCTGGAAAGTCTTTT CCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTAAGCCACTGTGCCCGGCCTGGAAAGTCTTTT A G MSH5-SAPCD1,MSH5 Ensembl:ENSG00000255152,Ensembl:ENSG00000204410 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs945166279 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17576285,Human_RBP_ID_23195185,Human_RBP_ID_25997184 19490 RMVar_ID_19490 Human_SNP_ID_272029083 A-to-I Human chr6 + 31749196 31749196 31749196 TCGGCCTCCCAAAGTGCTGGGATTACAGGCATAAGCCACTGTGCCCGGCCTGGAAAGTCTTTTCC TCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGTGCCCGGCCTGGAAAGTCTTTTCC A G MSH5-SAPCD1,MSH5 Ensembl:ENSG00000255152,Ensembl:ENSG00000204410 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1042233475 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17576285,Human_RBP_ID_23195185,Human_RBP_ID_25997184 19491 RMVar_ID_19491 Human_SNP_ID_272029148 A-to-I Human chr6 + 31749431 31749431 31749431 CAGCATCATGGCGCATGCCTCTAGTACCAGCTACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAA CAGCATCATGGCGCATGCCTCTAGTACCAGCTGCTCAGGAGGCTGAGGCAGGAGAATTGCTTGAA A G MSH5-SAPCD1,MSH5 Ensembl:ENSG00000255152,Ensembl:ENSG00000204410 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1428788472 Functional Loss SNV dbSNP153 33..33 33 - - - 19492 RMVar_ID_19492 Human_SNP_ID_272029155 A-to-I Human chr6 + 31749462 31749462 31749462 TACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAACTCGGGAGGTAGAGGTTGAAGTGAGCCCAGA TACTCAGGAGGCTGAGGCAGGAGAATTGCTTGTACTCGGGAGGTAGAGGTTGAAGTGAGCCCAGA A T MSH5-SAPCD1,MSH5 Ensembl:ENSG00000255152,Ensembl:ENSG00000204410 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1485159555 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23314642 19493 RMVar_ID_19493 Human_SNP_ID_272029577 A-to-I Human chr6 + 31751449 31751449 31751449 CCAGAGGTCCGGAGTTTGAGACCAGGCTGGCCAACATGGTGAAACCTCATCTCTACTAAAAATAC CCAGAGGTCCGGAGTTTGAGACCAGGCTGGCCGACATGGTGAAACCTCATCTCTACTAAAAATAC A G MSH5-SAPCD1,MSH5 Ensembl:ENSG00000255152,Ensembl:ENSG00000204410 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1038240321 Functional Loss SNV dbSNP153 33..33 33 - - - 19494 RMVar_ID_19494 Human_SNP_ID_272029616 A-to-I Human chr6 + 31751623 31751623 31751623 GCACCACTGCACTCCAGCCTGGACAACAGAGCAAGACTCTGTCTCAGAAAAAAAAAAAAAGATGT GCACCACTGCACTCCAGCCTGGACAACAGAGCGAGACTCTGTCTCAGAAAAAAAAAAAAAGATGT A G MSH5-SAPCD1,MSH5 Ensembl:ENSG00000255152,Ensembl:ENSG00000204410 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1223949497 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_754289 19495 RMVar_ID_19495 Human_SNP_ID_272029680 A-to-I Human chr6 + 31751917 31751917 31751917 GGTCACGATTTTGAGACCAGCCTGGCCAACACAGCGAAACCCTATCTCTACTAAAAATACAAAAT GGTCACGATTTTGAGACCAGCCTGGCCAACACGGCGAAACCCTATCTCTACTAAAAATACAAAAT A G MSH5-SAPCD1,MSH5 Ensembl:ENSG00000255152,Ensembl:ENSG00000204410 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1279816568 Functional Loss SNV dbSNP153 33..33 33 - - - 19496 RMVar_ID_19496 Human_SNP_ID_272029799 A-to-I Human chr6 + 31752350 31752350 31752350 AATTCCAGAACCTGGGAGGTGGAGGTTGCAGTAAGCCAAGATTGTGCTACTGCACTCTAGCCTGG AATTCCAGAACCTGGGAGGTGGAGGTTGCAGTGAGCCAAGATTGTGCTACTGCACTCTAGCCTGG A G MSH5-SAPCD1,MSH5 Ensembl:ENSG00000255152,Ensembl:ENSG00000204410 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1253474299 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22482626,Human_RBP_ID_23060459,Human_RBP_ID_26046357 19497 RMVar_ID_19497 Human_SNP_ID_272029876 A-to-I Human chr6 + 31752538 31752538 31752538 GGTCAAGAGATCGAGATCATTCTGGCCAACATAGTGAAACCCTGACTCTACTAAAAATACAACAA GGTCAAGAGATCGAGATCATTCTGGCCAACATGGTGAAACCCTGACTCTACTAAAAATACAACAA A G MSH5-SAPCD1,MSH5 Ensembl:ENSG00000255152,Ensembl:ENSG00000204410 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1219703090 Functional Loss SNV dbSNP153 33..33 33 - - - 19498 RMVar_ID_19498 Human_SNP_ID_272029891 A-to-I Human chr6 + 31752599 31752599 31752599 ACAATTAGCTGGGCATGGTGGCGCATACCTGCAGTCCCAGCTACTCGGGAGGCTGAGGCACGAAA ACAATTAGCTGGGCATGGTGGCGCATACCTGCGGTCCCAGCTACTCGGGAGGCTGAGGCACGAAA A G MSH5-SAPCD1,MSH5 Ensembl:ENSG00000255152,Ensembl:ENSG00000204410 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs995245370 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15787426,Human_RBP_ID_26046360 19499 RMVar_ID_19499 Human_SNP_ID_272030288 A-to-I Human chr6 + 31753832 31753832 31753832 CTCACTGCAACCTCCGCCTCCTGGGTTCAAGCAATTCTGCCTCAGCCTCCCGAGAAGTTGGGATT CTCACTGCAACCTCCGCCTCCTGGGTTCAAGCGATTCTGCCTCAGCCTCCCGAGAAGTTGGGATT A G MSH5-SAPCD1,MSH5 Ensembl:ENSG00000255152,Ensembl:ENSG00000204410 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs891490552 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26046372 19500 RMVar_ID_19500 Human_SNP_ID_272030297 A-to-I Human chr6 + 31753865 31753865 31753865 ATTCTGCCTCAGCCTCCCGAGAAGTTGGGATTACAAGCGCCCGCCACCATGCCTGGCAAATTTTT ATTCTGCCTCAGCCTCCCGAGAAGTTGGGATTGCAAGCGCCCGCCACCATGCCTGGCAAATTTTT A G MSH5-SAPCD1,MSH5 Ensembl:ENSG00000255152,Ensembl:ENSG00000204410 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs962440577 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15787486,Human_RBP_ID_25997268 19501 RMVar_ID_19501 Human_SNP_ID_272030314 A-to-I Human chr6 + 31753909 31753909 31753909 CACCATGCCTGGCAAATTTTTGTATTTTTAGTAGAGACAGGATTTCACCATGTTGGCCAGGCTGG CACCATGCCTGGCAAATTTTTGTATTTTTAGTGGAGACAGGATTTCACCATGTTGGCCAGGCTGG A G MSH5-SAPCD1,MSH5 Ensembl:ENSG00000255152,Ensembl:ENSG00000204410 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1233108435 Functional Loss SNV dbSNP153 33..33 33 - - - 19502 RMVar_ID_19502 Human_SNP_ID_272030760 A-to-I Human chr6 + 31755623 31755623 31755623 ACCTCAGATGATCTGCCTGCCCCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCATTGCAC ACCTCAGATGATCTGCCTGCCCCGGCCTCCCAGAGTGCTGGGATTACAGGCGTGAGCCATTGCAC A G MSH5-SAPCD1,MSH5 Ensembl:ENSG00000255152,Ensembl:ENSG00000204410 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs775554616 Functional Loss SNV dbSNP153 33..33 33 - - - 19503 RMVar_ID_19503 Human_SNP_ID_272038767 A-to-I Human chr6 - 31783424 31783424 31783424 CTCACTGCAACCTCCACCTCCCGGGTTCAAGCAGTACTTGTGCCTCAGCCTCTTGAGTAGCTGAG CTCACTGCAACCTCCACCTCCCGGGTTCAAGCCGTACTTGTGCCTCAGCCTCTTGAGTAGCTGAG T G VARS1 Ensembl:ENSG00000204394 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1041100770 Functional Loss SNV dbSNP153 33..33 33 - - - 19504 RMVar_ID_19504 Human_SNP_ID_272038779 A-to-I Human chr6 - 31783491 31783491 31783491 ATTTATTTATTTTTGAGAGAGGGTCTCACTCTATCGCCCAGGCTAGAGTGCAGTGGCACCATCTT ATTTATTTATTTTTGAGAGAGGGTCTCACTCTGTCGCCCAGGCTAGAGTGCAGTGGCACCATCTT T C VARS1 Ensembl:ENSG00000204394 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1396049405 Functional Loss SNV dbSNP153 33..33 33 - - - 19505 RMVar_ID_19505 Human_SNP_ID_272043552 A-to-I Human chr6 - 31802874 31802874 31802874 GAGTCTTGCCCTGTCGCCCAGGCTGGAGTGCAATGGCGTGATCTCGGCTCACCGCAACCTCTGCC GAGTCTTGCCCTGTCGCCCAGGCTGGAGTGCAGTGGCGTGATCTCGGCTCACCGCAACCTCTGCC T C LSM2 Ensembl:ENSG00000204392 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1256935618 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_754738 19506 RMVar_ID_19506 Human_SNP_ID_272043817 A-to-I Human chr6 - 31804249 31804248 31804249 TTCAAGCAATTCTCTGCCTCAGCCTCCCTAGTAGCTGTGATTACAAGTGCCCACCACCATGCCCG TTCAAGCAATTCTCTGCCTCAGCCTCCCTAGT_GCTGTGATTACAAGTGCCCACCACCATGCCCG CT C LSM2 Ensembl:ENSG00000204392 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1329784641 Functional Loss DEL dbSNP153 33..33 33 - - - 19507 RMVar_ID_19507 Human_SNP_ID_272043818 A-to-I Human chr6 - 31804249 31804249 31804249 TTCAAGCAATTCTCTGCCTCAGCCTCCCTAGTAGCTGTGATTACAAGTGCCCACCACCATGCCCG TTCAAGCAATTCTCTGCCTCAGCCTCCCTAGTGGCTGTGATTACAAGTGCCCACCACCATGCCCG T C LSM2 Ensembl:ENSG00000204392 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs999096988 Functional Loss SNV dbSNP153 33..33 33 - - - 19508 RMVar_ID_19508 Human_SNP_ID_272044087 A-to-I Human chr6 - 31805161 31805161 31805161 ATTCGGGAGGCTGAGGTGGGAGGATCACTTGAACCCAGGAGGTCAAGGCTGCAGTGAGCCATGAT ATTCGGGAGGCTGAGGTGGGAGGATCACTTGAGCCCAGGAGGTCAAGGCTGCAGTGAGCCATGAT T C LSM2 Ensembl:ENSG00000204392 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1001422238 Functional Loss SNV dbSNP153 33..33 33 - - - 19509 RMVar_ID_19509 Human_SNP_ID_272044272 A-to-I Human chr6 - 31805936 31805936 31805936 GAAGAAATAAATGGATAGGGTGCAGTGGCTCAAGCCTGTAATCCCAGCACTTTGGGAGGCTGAGG GAAGAAATAAATGGATAGGGTGCAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGG T A LSM2 Ensembl:ENSG00000204392 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1052623244 Functional Loss SNV dbSNP153 33..33 33 - - - 19510 RMVar_ID_19510 Human_SNP_ID_272044273 A-to-I Human chr6 - 31805936 31805936 31805936 GAAGAAATAAATGGATAGGGTGCAGTGGCTCAAGCCTGTAATCCCAGCACTTTGGGAGGCTGAGG GAAGAAATAAATGGATAGGGTGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGG T G LSM2 Ensembl:ENSG00000204392 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1052623244 Functional Loss SNV dbSNP153 33..33 33 - - - 19511 RMVar_ID_19511 Human_SNP_ID_272045723 A-to-I Human chr6 - 31810842 31810842 31810842 CCTGATGAGGCCGTAGCATATGGGGCTGCGGTACAAGCAGCCATCCTGATGGGGGACAAGTCTGA CCTGATGAGGCCGTAGCATATGGGGCTGCGGTGCAAGCAGCCATCCTGATGGGGGACAAGTCTGA T C HSPA1L Ensembl:ENSG00000204390 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1201797993 Functional Loss SNV dbSNP153 33..33 33 - - - 19512 RMVar_ID_19512 Human_SNP_ID_272051185 A-to-I Human chr6 + 31830830 31830830 31830830 TATTTTTGGTAGAGACAGGGTTTTACCGTGTTAGCCAGGATGGTCTCAATCTCCTGACCTCGGCT TATTTTTGGTAGAGACAGGGTTTTACCGTGTTGGCCAGGATGGTCTCAATCTCCTGACCTCGGCT A G AL671762.1 Ensembl:ENSG00000285565 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1422700963 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24157417 19513 RMVar_ID_19513 Human_SNP_ID_272053614 A-to-I Human chr6 + 31838105 31838105 31838105 GGTTCAAGCAATTCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCATGCGCCACCAGTCCCG GGTTCAAGCAATTCTGCCTCAGCCTCCCAAGTTGCTGGGATTACAGGCATGCGCCACCAGTCCCG A T SNHG32,AL671762.1 Ensembl:ENSG00000204387,Ensembl:ENSG00000285565 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1387274217 Functional Loss SNV dbSNP153 33..33 33 - - - 19514 RMVar_ID_19514 Human_SNP_ID_272053632 A-to-I Human chr6 + 31838172 31838172 31838172 TAATTTTTGTATTTTTAGTAGAGGGTTTCACCATGTTGGCCGGGCTGGTCTTGAACTCCTGACCA TAATTTTTGTATTTTTAGTAGAGGGTTTCACCGTGTTGGCCGGGCTGGTCTTGAACTCCTGACCA A G SNHG32,AL671762.1 Ensembl:ENSG00000204387,Ensembl:ENSG00000285565 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1279521458 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15788223 19515 RMVar_ID_19515 Human_SNP_ID_272053666 A-to-I Human chr6 + 31838314 31838314 31838314 TTTTATTTATTTTTTGTTTGAGATGGAGTTTCACTTTGTCGCCCAGGCTGGAGTGCAGTGGCACA TTTTATTTATTTTTTGTTTGAGATGGAGTTTCGCTTTGTCGCCCAGGCTGGAGTGCAGTGGCACA A G SNHG32,AL671762.1 Ensembl:ENSG00000204387,Ensembl:ENSG00000285565 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs914905194 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15788230 19516 RMVar_ID_19516 Human_SNP_ID_272053803 A-to-I Human chr6 + 31838889 31838889 31838889 AAATTAGCTGGGCATGGGTGGCGGGCGCCTGTAATTCCAGCTACTTGGGAGGCTGAGGCAGAAGA AAATTAGCTGGGCATGGGTGGCGGGCGCCTGTGATTCCAGCTACTTGGGAGGCTGAGGCAGAAGA A G SNHG32,AL671762.1 Ensembl:ENSG00000204387,Ensembl:ENSG00000285565 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1267782160 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25997723 19517 RMVar_ID_19517 Human_SNP_ID_272058748 A-to-I Human chr6 - 31855831 31855831 31855831 AGAATCTAGGCCAGGCGCTGTGGCTCACACCTATAATCCCAGCACTTTGGGAGGCAGAGGCAAGC AGAATCTAGGCCAGGCGCTGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCAGAGGCAAGC T C RF00017-4520,RF00017-4531,lnc-BBS5-6 RNACentral:URS000099C2D3,RNACentral:URS000098F531,RNACentral:URS0000E2127A SRP RNA,SRP RNA,lincRNA intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1205611442 Functional Loss SNV dbSNP153 33..33 33 - - - 19518 RMVar_ID_19518 Human_SNP_ID_272059250 A-to-I Human chr6 - 31858286 31858286 31858286 TTTAATTTTTAGTAGAGACAAAGTCTCACTATATTGCCTAGGTTGGTCTCAAACTGCTGAGCTCA TTTAATTTTTAGTAGAGACAAAGTCTCACTATGTTGCCTAGGTTGGTCTCAAACTGCTGAGCTCA T C NEU1 Ensembl:ENSG00000204386 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1428790720 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17576825 19519 RMVar_ID_19519 Human_SNP_ID_272059417 A-to-I Human chr6 - 31858996 31858996 31858996 CTTTTTTTGAGACAGGGCTCGCTCTGTCACCCAGGCTGGAGTGCAGTTGCACAATCACGGCTCAC CTTTTTTTGAGACAGGGCTCGCTCTGTCACCCGGGCTGGAGTGCAGTTGCACAATCACGGCTCAC T C NEU1 Ensembl:ENSG00000204386 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs961881462 Functional Loss SNV dbSNP153 33..33 33 - - - 19520 RMVar_ID_19520 Human_SNP_ID_272072423 A-to-I Human chr6 + 31907980 31907980 31907980 GCAATTCTCCTGCCTCAGCCTCCTGAGTAGCTAGGATTACGGACGTCTGCCACCACGCCCAGCTA GCAATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACGGACGTCTGCCACCACGCCCAGCTA A G C2 Ensembl:ENSG00000166278 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006687030 Functional Loss SNV dbSNP153 33..33 33 - - - 19521 RMVar_ID_19521 Human_SNP_ID_272072424 A-to-I Human chr6 + 31907980 31907980 31907980 GCAATTCTCCTGCCTCAGCCTCCTGAGTAGCTAGGATTACGGACGTCTGCCACCACGCCCAGCTA GCAATTCTCCTGCCTCAGCCTCCTGAGTAGCTTGGATTACGGACGTCTGCCACCACGCCCAGCTA A T C2 Ensembl:ENSG00000166278 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006687030 Functional Loss SNV dbSNP153 33..33 33 - - - 19522 RMVar_ID_19522 Human_SNP_ID_272072501 A-to-I Human chr6 + 31908268 31908268 31908268 CTCCTGCCTTGGCCTCCCAAAGTGTTGAGTCTACAGGCATGAGCCACCGTGCTCGGCCCAGATAA CTCCTGCCTTGGCCTCCCAAAGTGTTGAGTCTGCAGGCATGAGCCACCGTGCTCGGCCCAGATAA A G C2 Ensembl:ENSG00000166278 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs568331554 Functional Loss SNV dbSNP153 33..33 33 - - - 19523 RMVar_ID_19523 Human_SNP_ID_272089225 A-to-I Human chr6 + 31971933 31971933 31971933 TCTGCGCTCAGATCAAGAATCCAGTTACCTCAAAGCTCCCCAACTTCCACCTCCGCAGAGCTATG TCTGCGCTCAGATCAAGAATCCAGTTACCTCAGAGCTCCCCAACTTCCACCTCCGCAGAGCTATG A G STK19 Ensembl:ENSG00000204344 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1191109249 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_791755 Human_Splice_Rec_756496,Human_Splice_Rec_756510 19524 RMVar_ID_19524 Human_SNP_ID_272090931 A-to-I Human chr6 + 31977623 31977623 31977623 CACCCGTCTCAGCCTGCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCATCTGGCCTATTTTT CACCCGTCTCAGCCTGCCAAAGTGCTGGGATTGCAGGCATGAGCCACCGCATCTGGCCTATTTTT A G STK19 Ensembl:ENSG00000204344 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1162461101 Functional Loss SNV dbSNP153 33..33 33 - - - 19525 RMVar_ID_19525 Human_SNP_ID_272120737 A-to-I Human chr6 - 32123589 32123589 32123589 GGTCAGGAGATCAAGACCATTCGGGCTAACACAGTGAAGCGCCATCTCTACTAAAAATACAAAAA GGTCAGGAGATCAAGACCATTCGGGCTAACACGGTGAAGCGCCATCTCTACTAAAAATACAAAAA T C ATF6B Ensembl:ENSG00000213676 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1267880846 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_336883 19526 RMVar_ID_19526 Human_SNP_ID_272128549 A-to-I Human chr6 + 32157050 32157050 32157050 AAAATACAAAAAAAATTTAGCTGAATGTGGGCACACGCTTGTAATCCCAGCTACTCAGGATGCTG AAAATACAAAAAAAATTTAGCTGAATGTGGGCCCACGCTTGTAATCCCAGCTACTCAGGATGCTG A C PPT2,PPT2-EGFL8 Ensembl:ENSG00000221988,Ensembl:ENSG00000258388 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256627584 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91685,RMVar_hsa_circ_237839 19527 RMVar_ID_19527 Human_SNP_ID_272128556 A-to-I Human chr6 + 32157101 32157101 32157101 TACTCAGGATGCTGAGTCAGGAGAATTGCTTGAACCCGGGAGGCAGATGTTGCAGTGAGCGGAGA TACTCAGGATGCTGAGTCAGGAGAATTGCTTGTACCCGGGAGGCAGATGTTGCAGTGAGCGGAGA A T PPT2,PPT2-EGFL8 Ensembl:ENSG00000221988,Ensembl:ENSG00000258388 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs565457597 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91685,RMVar_hsa_circ_237839 19528 RMVar_ID_19528 Human_SNP_ID_272129435 A-to-I Human chr6 + 32160548 32160548 32160548 AAAAATTAGTGGGCCTGGTGGCGCACGCCTGTAGTTCCAGCTACTCAGGAGGCTGAGGCAGGAGA AAAAATTAGTGGGCCTGGTGGCGCACGCCTGTGGTTCCAGCTACTCAGGAGGCTGAGGCAGGAGA A G PPT2,PPT2-EGFL8 Ensembl:ENSG00000221988,Ensembl:ENSG00000258388 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1226743367 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91685,RMVar_hsa_circ_237839 19529 RMVar_ID_19529 Human_SNP_ID_272130585 A-to-I Human chr6 + 32165663 32165663 32165663 AAAATTAGCCAGGCGTGGTGGCGCATGCCTGTAATCCCAGCTATTTGGGAGGCTGAGGCAGGAGA AAAATTAGCCAGGCGTGGTGGCGCATGCCTGTGATCCCAGCTATTTGGGAGGCTGAGGCAGGAGA A G EGFL8,PPT2-EGFL8 Ensembl:ENSG00000241404,Ensembl:ENSG00000258388 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1427742267 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91685,RMVar_hsa_circ_237839 19530 RMVar_ID_19530 Human_SNP_ID_272245116 A-to-I Human chr6 - 32581567 32581565 32581568 GTGGAGCACCCAAGCGTGACAAGCCCTCTCACAGTGGAATGGAGTGAGCAGCTTTCTGACTTCCT GTGGAGCACCCAAGCGTGACAAGCCCTCTCA___TGGAATGGAGTGAGCAGCTTTCTGACTTCCT ACTG A HLA-DRB1 Ensembl:ENSG00000196126 Protein coding CDS GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1377451889 Functional Loss DEL dbSNP153 32..34 33 - - - Human_Splice_Rec_759479 Human_miRNA_ID_2047060,Human_miRNA_ID_2672243,Human_miRNA_ID_2968112 RMVar_hsa_circ_93890,RMVar_hsa_circ_237846 19531 RMVar_ID_19531 Human_SNP_ID_272245117 A-to-I Human chr6 - 32581567 32581567 32581567 GTGGAGCACCCAAGCGTGACAAGCCCTCTCACAGTGGAATGGAGTGAGCAGCTTTCTGACTTCCT GTGGAGCACCCAAGCGTGACAAGCCCTCTCACGGTGGAATGGAGTGAGCAGCTTTCTGACTTCCT T C HLA-DRB1 Ensembl:ENSG00000196126 Protein coding CDS GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs17878677 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_Splice_Rec_759479 Human_miRNA_ID_2047060,Human_miRNA_ID_2672243,Human_miRNA_ID_2968112 RMVar_hsa_circ_93890,RMVar_hsa_circ_237846 19532 RMVar_ID_19532 Human_SNP_ID_272246435 A-to-I Human chr6 - 32583744 32583744 32583744 GAGACCTTGATTATCTCGGTCCTTAGAGATGCAGGGAAGGGAAATGTAAGGTGTGTGTGGTTGGG GAGACCTTGATTATCTCGGTCCTTAGAGATGCGGGGAAGGGAAATGTAAGGTGTGTGTGGTTGGG T C HLA-DRB1 Ensembl:ENSG00000196126 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs72850280 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93890,RMVar_hsa_circ_237846 19533 RMVar_ID_19533 Human_SNP_ID_272247776 A-to-I Human chr6 - 32585226 32585226 32585226 TGTACCAGGCTGTTTCTTAGAGTGGGGACAGAAATGCAAGGGCTGCTAGTTCTGATGTATAGGAG TGTACCAGGCTGTTTCTTAGAGTGGGGACAGAGATGCAAGGGCTGCTAGTTCTGATGTATAGGAG T C HLA-DRB1 Ensembl:ENSG00000196126 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs9270016 Functional Loss SNV dbSNP153 33..33 33 - - - 19534 RMVar_ID_19534 Human_SNP_ID_272248456 A-to-I Human chr6 - 32586479 32586479 32586479 AAAAACCAAGAGAACATCATGTGTGTAAGTCCAGGAAAATAGATTATTTTCAAGGAGAAGGGAGA AAAAACCAAGAGAACATCATGTGTGTAAGTCCTGGAAAATAGATTATTTTCAAGGAGAAGGGAGA T A HLA-DRB1 Ensembl:ENSG00000196126 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs200889932 Functional Loss SNV dbSNP153 33..33 33 - - - 19535 RMVar_ID_19535 Human_SNP_ID_272248457 A-to-I Human chr6 - 32586479 32586479 32586479 AAAAACCAAGAGAACATCATGTGTGTAAGTCCAGGAAAATAGATTATTTTCAAGGAGAAGGGAGA AAAAACCAAGAGAACATCATGTGTGTAAGTCCCGGAAAATAGATTATTTTCAAGGAGAAGGGAGA T G HLA-DRB1 Ensembl:ENSG00000196126 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs200889932 Functional Loss SNV dbSNP153 33..33 33 - - - 19536 RMVar_ID_19536 Human_SNP_ID_272249283 A-to-I Human chr6 - 32587580 32587580 32587580 TTCCAGGGAGACCGAATCGGGGGAAAGCCCTGATGTGTTAAATTATGTGGAGGGAGAGAAAGAAA TTCCAGGGAGACCGAATCGGGGGAAAGCCCTGGTGTGTTAAATTATGTGGAGGGAGAGAAAGAAA T C HLA-DRB1 Ensembl:ENSG00000196126 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs9270150 Functional Loss SNV dbSNP153 33..33 33 - - - 19537 RMVar_ID_19537 Human_SNP_ID_272249284 A-to-I Human chr6 - 32587580 32587580 32587580 TTCCAGGGAGACCGAATCGGGGGAAAGCCCTGATGTGTTAAATTATGTGGAGGGAGAGAAAGAAA TTCCAGGGAGACCGAATCGGGGGAAAGCCCTGCTGTGTTAAATTATGTGGAGGGAGAGAAAGAAA T G HLA-DRB1 Ensembl:ENSG00000196126 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs9270150 Functional Loss SNV dbSNP153 33..33 33 - - - 19538 RMVar_ID_19538 Human_SNP_ID_272275249 A-to-I Human chr6 - 32662417 32662415 32662417 ATGCAGGGACCATAGTATGTTATTTATCTTTGAATTCTCAGTGATTGTCAAATTTATATTTGTTG ATGCAGGGACCATAGTATGTTATTTATCTTTG__TTCTCAGTGATTGTCAAATTTATATTTGTTG ATT A HLA-DQB1 Ensembl:ENSG00000179344 Protein coding exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs9280031 Functional Loss DEL dbSNP153 33..34 33 - - - Human_Splice_Rec_759575 19539 RMVar_ID_19539 Human_SNP_ID_272275255 A-to-I Human chr6 - 32662417 32662417 32662417 ATGCAGGGACCATAGTATGTTATTTATCTTTGAATTCTCAGTGATTGTCAAATTTATATTTGTTG ATGCAGGGACCATAGTATGTTATTTATCTTTGTATTCTCAGTGATTGTCAAATTTATATTTGTTG T A HLA-DQB1 Ensembl:ENSG00000179344 Protein coding exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs9274112 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_759575 19540 RMVar_ID_19540 Human_SNP_ID_272275256 A-to-I Human chr6 - 32662417 32662417 32662417 ATGCAGGGACCATAGTATGTTATTTATCTTTGAATTCTCAGTGATTGTCAAATTTATATTTGTTG ATGCAGGGACCATAGTATGTTATTTATCTTTGGATTCTCAGTGATTGTCAAATTTATATTTGTTG T C HLA-DQB1 Ensembl:ENSG00000179344 Protein coding exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs9274112 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_759575 19541 RMVar_ID_19541 Human_SNP_ID_272275280 A-to-I Human chr6 - 32662428 32662428 32662428 ACATTCTATAAATGCAGGGACCATAGTATGTTATTTATCTTTGAATTCTCAGTGATTGTCAAATT ACATTCTATAAATGCAGGGACCATAGTATGTTTTTTATCTTTGAATTCTCAGTGATTGTCAAATT T A HLA-DQB1 Ensembl:ENSG00000179344 Protein coding exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs9274115 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_759575 19542 RMVar_ID_19542 Human_SNP_ID_272275281 A-to-I Human chr6 - 32662428 32662428 32662428 ACATTCTATAAATGCAGGGACCATAGTATGTTATTTATCTTTGAATTCTCAGTGATTGTCAAATT ACATTCTATAAATGCAGGGACCATAGTATGTTGTTTATCTTTGAATTCTCAGTGATTGTCAAATT T C HLA-DQB1 Ensembl:ENSG00000179344 Protein coding exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs9274115 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_759575 19543 RMVar_ID_19543 Human_SNP_ID_272275282 A-to-I Human chr6 - 32662428 32662428 32662428 ACATTCTATAAATGCAGGGACCATAGTATGTTATTTATCTTTGAATTCTCAGTGATTGTCAAATT ACATTCTATAAATGCAGGGACCATAGTATGTTCTTTATCTTTGAATTCTCAGTGATTGTCAAATT T G HLA-DQB1 Ensembl:ENSG00000179344 Protein coding exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs9274115 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_759575 19544 RMVar_ID_19544 Human_SNP_ID_272275293 A-to-I Human chr6 - 32662436 32662434 32662436 TAGATTGCACATTCTATAAATGCAGGGACCATAGTATGTTATTTATCTTTGAATTCTCAGTGATT TAGATTGCACATTCTATAAATGCAGGGACCAT__TATGTTATTTATCTTTGAATTCTCAGTGATT ACT A HLA-DQB1 Ensembl:ENSG00000179344 Protein coding exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs9280032 Functional Loss DEL dbSNP153 33..34 33 - - - Human_Splice_Rec_759575 19545 RMVar_ID_19545 Human_SNP_ID_272275298 A-to-I Human chr6 - 32662436 32662436 32662436 TAGATTGCACATTCTATAAATGCAGGGACCATAGTATGTTATTTATCTTTGAATTCTCAGTGATT TAGATTGCACATTCTATAAATGCAGGGACCATTGTATGTTATTTATCTTTGAATTCTCAGTGATT T A HLA-DQB1 Ensembl:ENSG00000179344 Protein coding exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4360168 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_759575 19546 RMVar_ID_19546 Human_SNP_ID_272275299 A-to-I Human chr6 - 32662436 32662436 32662436 TAGATTGCACATTCTATAAATGCAGGGACCATAGTATGTTATTTATCTTTGAATTCTCAGTGATT TAGATTGCACATTCTATAAATGCAGGGACCATGGTATGTTATTTATCTTTGAATTCTCAGTGATT T C HLA-DQB1 Ensembl:ENSG00000179344 Protein coding exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4360168 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_759575 19547 RMVar_ID_19547 Human_SNP_ID_272275856 A-to-I Human chr6 - 32662718 32662718 32662718 AAGAGAATAAAGGAAATGTGATAAAGTGGCCTAAAAGGAAAGGATGAGATGTGTAAAAGAGGCGG AAGAGAATAAAGGAAATGTGATAAAGTGGCCTGAAAGGAAAGGATGAGATGTGTAAAAGAGGCGG T C HLA-DQB1 Ensembl:ENSG00000179344 Protein coding exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs9274183 Functional Loss SNV dbSNP153 33..33 33 - - - 19548 RMVar_ID_19548 Human_SNP_ID_272277524 A-to-I Human chr6 - 32663874 32663874 32663874 TAATTTCTTAGAAAAGCTGAACAAATAGCACTATGCAAAGATCAGAAGTTTGGGAATAAATAGGT TAATTTCTTAGAAAAGCTGAACAAATAGCACTTTGCAAAGATCAGAAGTTTGGGAATAAATAGGT T A HLA-DQB1 Ensembl:ENSG00000179344 Protein coding exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs281863149 Functional Loss SNV dbSNP153 33..33 33 - - - 19549 RMVar_ID_19549 Human_SNP_ID_272277832 A-to-I Human chr6 - 32664019 32664019 32664019 AATTATTTTCTAACATTTTGCTTAATGCTTTCAAGTAAACTCTTACTGACTTGGATCTTAATAGA AATTATTTTCTAACATTTTGCTTAATGCTTTCGAGTAAACTCTTACTGACTTGGATCTTAATAGA T C HLA-DQB1 Ensembl:ENSG00000179344 Protein coding exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs281862707 Functional Loss SNV dbSNP153 33..33 33 - - - 19550 RMVar_ID_19550 Human_SNP_ID_272277833 A-to-I Human chr6 - 32664019 32664019 32664019 AATTATTTTCTAACATTTTGCTTAATGCTTTCAAGTAAACTCTTACTGACTTGGATCTTAATAGA AATTATTTTCTAACATTTTGCTTAATGCTTTCCAGTAAACTCTTACTGACTTGGATCTTAATAGA T G HLA-DQB1 Ensembl:ENSG00000179344 Protein coding exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs281862707 Functional Loss SNV dbSNP153 33..33 33 - - - 19551 RMVar_ID_19551 Human_SNP_ID_272277874 A-to-I Human chr6 - 32664039 32664039 32664039 GCTTACAAATGAACTTTATCAATTATTTTCTAACATTTTGCTTAATGCTTTCAAGTAAACTCTTA GCTTACAAATGAACTTTATCAATTATTTTCTATCATTTTGCTTAATGCTTTCAAGTAAACTCTTA T A HLA-DQB1 Ensembl:ENSG00000179344 Protein coding exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs281862690 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7593663 GWAS_ID_1678 19552 RMVar_ID_19552 Human_SNP_ID_272277875 A-to-I Human chr6 - 32664039 32664039 32664039 GCTTACAAATGAACTTTATCAATTATTTTCTAACATTTTGCTTAATGCTTTCAAGTAAACTCTTA GCTTACAAATGAACTTTATCAATTATTTTCTACCATTTTGCTTAATGCTTTCAAGTAAACTCTTA T G HLA-DQB1 Ensembl:ENSG00000179344 Protein coding exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs281862690 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7593663 GWAS_ID_1678 19553 RMVar_ID_19553 Human_SNP_ID_272277903 A-to-I Human chr6 - 32664051 32664051 32664051 AAAAAAACAGAGGCTTACAAATGAACTTTATCAATTATTTTCTAACATTTTGCTTAATGCTTTCA AAAAAAACAGAGGCTTACAAATGAACTTTATCTATTATTTTCTAACATTTTGCTTAATGCTTTCA T A HLA-DQB1 Ensembl:ENSG00000179344 Protein coding exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs281862679 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7593663 19554 RMVar_ID_19554 Human_SNP_ID_272277904 A-to-I Human chr6 - 32664051 32664051 32664051 AAAAAAACAGAGGCTTACAAATGAACTTTATCAATTATTTTCTAACATTTTGCTTAATGCTTTCA AAAAAAACAGAGGCTTACAAATGAACTTTATCCATTATTTTCTAACATTTTGCTTAATGCTTTCA T G HLA-DQB1 Ensembl:ENSG00000179344 Protein coding exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs281862679 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7593663 19555 RMVar_ID_19555 Human_SNP_ID_272280001 A-to-I Human chr6 - 32665264 32665264 32665264 GGCTTTCCTCCCTTTCCTGGATGTAGGAAGGCAGATTCCAGAAGCCCGCAAAGAAGGCGGGCAGA GGCTTTCCTCCCTTTCCTGGATGTAGGAAGGCTGATTCCAGAAGCCCGCAAAGAAGGCGGGCAGA T A HLA-DQB1 Ensembl:ENSG00000179344 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs9274428 Functional Loss SNV dbSNP153 33..33 33 - - - 19556 RMVar_ID_19556 Human_SNP_ID_272280002 A-to-I Human chr6 - 32665264 32665264 32665264 GGCTTTCCTCCCTTTCCTGGATGTAGGAAGGCAGATTCCAGAAGCCCGCAAAGAAGGCGGGCAGA GGCTTTCCTCCCTTTCCTGGATGTAGGAAGGCGGATTCCAGAAGCCCGCAAAGAAGGCGGGCAGA T C HLA-DQB1 Ensembl:ENSG00000179344 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs9274428 Functional Loss SNV dbSNP153 33..33 33 - - - 19557 RMVar_ID_19557 Human_SNP_ID_272280003 A-to-I Human chr6 - 32665264 32665264 32665264 GGCTTTCCTCCCTTTCCTGGATGTAGGAAGGCAGATTCCAGAAGCCCGCAAAGAAGGCGGGCAGA GGCTTTCCTCCCTTTCCTGGATGTAGGAAGGCCGATTCCAGAAGCCCGCAAAGAAGGCGGGCAGA T G HLA-DQB1 Ensembl:ENSG00000179344 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs9274428 Functional Loss SNV dbSNP153 33..33 33 - - - 19558 RMVar_ID_19558 Human_SNP_ID_272280351 A-to-I Human chr6 - 32665449 32665449 32665449 GGACCTATCTCGTCATTCCGTTGAACTCTCAGATTTATGTGGATAACTTTATCTCTGAGGTATCC GGACCTATCTCGTCATTCCGTTGAACTCTCAGTTTTATGTGGATAACTTTATCTCTGAGGTATCC T A HLA-DQB1 Ensembl:ENSG00000179344 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs9274441 Functional Loss SNV dbSNP153 33..33 33 - - - 19559 RMVar_ID_19559 Human_SNP_ID_272280352 A-to-I Human chr6 - 32665449 32665449 32665449 GGACCTATCTCGTCATTCCGTTGAACTCTCAGATTTATGTGGATAACTTTATCTCTGAGGTATCC GGACCTATCTCGTCATTCCGTTGAACTCTCAGGTTTATGTGGATAACTTTATCTCTGAGGTATCC T C HLA-DQB1 Ensembl:ENSG00000179344 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs9274441 Functional Loss SNV dbSNP153 33..33 33 - - - 19560 RMVar_ID_19560 Human_SNP_ID_272366993 A-to-I Human chr6 - 33005309 33005309 33005309 TTTTGTATTTTAAGTAGAGACGGGGTTTCATCATGTTGGCCAGGATGGCCTCCATCTCTTGACCT TTTTGTATTTTAAGTAGAGACGGGGTTTCATCTTGTTGGCCAGGATGGCCTCCATCTCTTGACCT T A HLA-DOA Ensembl:ENSG00000204252 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs982217212 Functional Loss SNV dbSNP153 33..33 33 - - - 19561 RMVar_ID_19561 Human_SNP_ID_272367017 A-to-I Human chr6 - 33005415 33005415 33005415 TGATCTCAGCTCACTGCAACCTCCACCTCCTGAGTTCAAGCCATTCTCCTGCCTCAGCCTCCTGA TGATCTCAGCTCACTGCAACCTCCACCTCCTGGGTTCAAGCCATTCTCCTGCCTCAGCCTCCTGA T C HLA-DOA Ensembl:ENSG00000204252 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1401566574 Functional Loss SNV dbSNP153 33..33 33 - - - 19562 RMVar_ID_19562 Human_SNP_ID_272367022 A-to-I Human chr6 - 33005440 33005440 33005440 GTCACCAGGCTGGAGTGCCATGGCATGATCTCAGCTCACTGCAACCTCCACCTCCTGAGTTCAAG GTCACCAGGCTGGAGTGCCATGGCATGATCTCGGCTCACTGCAACCTCCACCTCCTGAGTTCAAG T C HLA-DOA Ensembl:ENSG00000204252 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1461446263 Functional Loss SNV dbSNP153 33..33 33 - - - 19563 RMVar_ID_19563 Human_SNP_ID_272367075 A-to-I Human chr6 - 33005646 33005646 33005646 TTGAGCCCAGGAGTTCAAGGCTGCAGTGAGCCAAGATTGCGCCACTGCACTCCAGCCTAGGTGAC TTGAGCCCAGGAGTTCAAGGCTGCAGTGAGCCGAGATTGCGCCACTGCACTCCAGCCTAGGTGAC T C HLA-DOA Ensembl:ENSG00000204252 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs944350737 Functional Loss SNV dbSNP153 33..33 33 - - - 19564 RMVar_ID_19564 Human_SNP_ID_272431019 A-to-I Human chr6 - 33257974 33257974 33257974 GTCTTGCTCTGTCACCCAAGCTGGAATGCAGTAGTGTGATCATGGCTCACTGTAGCCTCAACCTC GTCTTGCTCTGTCACCCAAGCTGGAATGCAGTGGTGTGATCATGGCTCACTGTAGCCTCAACCTC T C VPS52 Ensembl:ENSG00000223501 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1013741055 Functional Loss SNV dbSNP153 33..33 33 - - - 19565 RMVar_ID_19565 Human_SNP_ID_272431572 A-to-I Human chr6 + 33260250 33260250 33260250 TTGCTGTGTTGCCAAGGGTAGACTACAATGTCATGATCATGGCTCGCTGTAATCTCGAACTCCTG TTGCTGTGTTGCCAAGGGTAGACTACAATGTCCTGATCATGGCTCGCTGTAATCTCGAACTCCTG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1267157670 Functional Loss SNV dbSNP153 33..33 33 - - - 19566 RMVar_ID_19566 Human_SNP_ID_272431586 A-to-I Human chr6 - 33260278 33260278 33260278 ACAAAGGCGAGAGGACCACTTTGAAATCCAGGAGTTCGAGATTACAGCGAGCCATGATCATGACA ACAAAGGCGAGAGGACCACTTTGAAATCCAGGTGTTCGAGATTACAGCGAGCCATGATCATGACA T A VPS52 Ensembl:ENSG00000223501 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1345878267 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8642941,Human_RBP_ID_15791561 19567 RMVar_ID_19567 Human_SNP_ID_272431589 A-to-I Human chr6 - 33260301 33260301 33260301 CTGTAGTTCTAGCTATTTGGGAGACAAAGGCGAGAGGACCACTTTGAAATCCAGGAGTTCGAGAT CTGTAGTTCTAGCTATTTGGGAGACAAAGGCGGGAGGACCACTTTGAAATCCAGGAGTTCGAGAT T C VPS52 Ensembl:ENSG00000223501 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs916715807 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15791562 19568 RMVar_ID_19568 Human_SNP_ID_272431592 A-to-I Human chr6 + 33260324 33260324 33260324 GTGGTCCTCTCGCCTTTGTCTCCCAAATAGCTAGAACTACAGGTGCATACCACCATGCCTGGCTT GTGGTCCTCTCGCCTTTGTCTCCCAAATAGCTGGAACTACAGGTGCATACCACCATGCCTGGCTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1194634342 Functional Loss SNV dbSNP153 33..33 33 - - - 19569 RMVar_ID_19569 Human_SNP_ID_272443578 A-to-I Human chr6 - 33300718 33300718 33300718 CTGGTGATCCGCCCGCCTCGGCCTCCCAAAGTATTGGGATTACCCGCGTGAGCCACCGCGCCCGG CTGGTGATCCGCCCGCCTCGGCCTCCCAAAGTGTTGGGATTACCCGCGTGAGCCACCGCGCCCGG T C TAPBP Ensembl:ENSG00000231925 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs372602637 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4884679,Human_RBP_ID_23195323,Human_RBP_ID_25999123 19570 RMVar_ID_19570 Human_SNP_ID_272443979 A-to-I Human chr6 - 33302221 33302221 33302221 GGATCGCTTGAATCTGGGAGGGTGAGGCTGCAATGAGCTAAGGTTGTCCCACTGTACTCCAGCCT GGATCGCTTGAATCTGGGAGGGTGAGGCTGCAGTGAGCTAAGGTTGTCCCACTGTACTCCAGCCT T C TAPBP Ensembl:ENSG00000231925 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1030063894 Functional Loss SNV dbSNP153 33..33 33 - - - 19571 RMVar_ID_19571 Human_SNP_ID_272444117 A-to-I Human chr6 - 33302784 33302784 33302784 ACAAAAAATTAGCCAGATGTGACGGCACCTGTAATCCCAGCTACTCGGGAGACTGGGGCAGGAGA ACAAAAAATTAGCCAGATGTGACGGCACCTGTCATCCCAGCTACTCGGGAGACTGGGGCAGGAGA T G TAPBP Ensembl:ENSG00000231925 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs540386359 Functional Loss SNV dbSNP153 33..33 33 - - - 19572 RMVar_ID_19572 Human_SNP_ID_272444124 A-to-I Human chr6 - 33302841 33302841 33302841 GTCAGGAGTTCAAGACCAGCTTAGCCAACATGATGAAACCCCATCTCTACTAAAAATACAAAAAA GTCAGGAGTTCAAGACCAGCTTAGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAAA T C TAPBP Ensembl:ENSG00000231925 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1424269928 Functional Loss SNV dbSNP153 33..33 33 - - - 19573 RMVar_ID_19573 Human_SNP_ID_272444221 A-to-I Human chr6 - 33303256 33303256 33303256 CACCACCACGCCTGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGTCAGGC CACCACCACGCCTGGCTAATTTTTGTATTTTTGGTAGAGACGGGGTTTCACCATGTTGGTCAGGC T C TAPBP Ensembl:ENSG00000231925 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs955590412 Functional Loss SNV dbSNP153 33..33 33 - - - 19574 RMVar_ID_19574 Human_SNP_ID_272444224 A-to-I Human chr6 - 33303271 33303271 33303271 GGGATTACAGGCACCCACCACCACGCCTGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCA GGGATTACAGGCACCCACCACCACGCCTGGCTGATTTTTGTATTTTTAGTAGAGACGGGGTTTCA T C TAPBP Ensembl:ENSG00000231925 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs989531286 Functional Loss SNV dbSNP153 33..33 33 - - - 19575 RMVar_ID_19575 Human_SNP_ID_272445267 A-to-I Human chr6 - 33307219 33307219 33307219 TAGTGGCATGATTTCAGCTTACGGCAACCTCTACCTCCCAGGTTCAAGTGATTCTTCTGCCTCAG TAGTGGCATGATTTCAGCTTACGGCAACCTCTGCCTCCCAGGTTCAAGTGATTCTTCTGCCTCAG T C TAPBP Ensembl:ENSG00000231925 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs543520076 Functional Loss SNV dbSNP153 33..33 33 - - - 19576 RMVar_ID_19576 Human_SNP_ID_272445354 A-to-I Human chr6 - 33307540 33307540 33307540 AAAATTAGCTGGGCACGGTTGTGGACGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA AAAATTAGCTGGGCACGGTTGTGGACGCCTGTGATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA T C TAPBP Ensembl:ENSG00000231925 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1298073799 Functional Loss SNV dbSNP153 33..33 33 - - - 19577 RMVar_ID_19577 Human_SNP_ID_272445847 A-to-I Human chr6 - 33309696 33309696 33309696 AAAAAAAAGGTTGGGTGTCGTGGCATGTACCTATGGTCCCAGCTACTCGGGAGGCTGTGTTGGGA AAAAAAAAGGTTGGGTGTCGTGGCATGTACCTGTGGTCCCAGCTACTCGGGAGGCTGTGTTGGGA T C TAPBP Ensembl:ENSG00000231925 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1214128692 Functional Loss SNV dbSNP153 33..33 33 - - - 19578 RMVar_ID_19578 Human_SNP_ID_272468155 A-to-I Human chr6 + 33398484 33398484 33398484 TCTTTTCTTTCAATTTTATTTTATTTTTTTTGAGACAGAGTCTCGCTCTATCGCCCAGGCTGGAG TCTTTTCTTTCAATTTTATTTTATTTTTTTTGGGACAGAGTCTCGCTCTATCGCCCAGGCTGGAG A G KIFC1 Ensembl:ENSG00000237649 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs959634352 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7594614 RMVar_hsa_circ_107733,RMVar_hsa_circ_237859 19579 RMVar_ID_19579 Human_SNP_ID_272468162 A-to-I Human chr6 + 33398501 33398501 33398501 ATTTTATTTTTTTTGAGACAGAGTCTCGCTCTATCGCCCAGGCTGGAGTGCAGTGGCTCAATCTC ATTTTATTTTTTTTGAGACAGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCTCAATCTC A G KIFC1 Ensembl:ENSG00000237649 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1331844568 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2972951,Human_miRNA_ID_3006135 RMVar_hsa_circ_107733,RMVar_hsa_circ_237859 19580 RMVar_ID_19580 Human_SNP_ID_272468311 A-to-I Human chr6 + 33399273 33399273 33399273 AGCCAGACGTGATGGCCCGTGCCTGTAATCCCAGCTACTCTGGAGGCTGAGGCAGGAGAATTGCT AGCCAGACGTGATGGCCCGTGCCTGTAATCCCGGCTACTCTGGAGGCTGAGGCAGGAGAATTGCT A G KIFC1 Ensembl:ENSG00000237649 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs570884731 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107733,RMVar_hsa_circ_237859 19581 RMVar_ID_19581 Human_SNP_ID_272532354 A-to-I Human chr6 + 33653329 33653329 33653329 TAAAGACAGGATTTCGTCATGTTGCCCAGGCCAGTCTCGAACTCCTGGCCTCAAGTGATCCTCCT TAAAGACAGGATTTCGTCATGTTGCCCAGGCCGGTCTCGAACTCCTGGCCTCAAGTGATCCTCCT A G ITPR3 Ensembl:ENSG00000096433 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1173284115 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99929,RMVar_hsa_circ_100275,RMVar_hsa_circ_237872,RMVar_hsa_circ_237873 19582 RMVar_ID_19582 Human_SNP_ID_272544498 A-to-I Human chr6 - 33696821 33696821 33696821 GTGGAAGTGGGTTCTTAACCTCGTCTGTGTCTAGACTCCTCAGGATGTTCTGAAATGCATAAAAT GTGGAAGTGGGTTCTTAACCTCGTCTGTGTCTGGACTCCTCAGGATGTTCTGAAATGCATAAAAT T C UQCC2 Ensembl:ENSG00000137288 Protein coding exon GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs940110536 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1671955,Human_RBP_ID_3004010,Human_RBP_ID_3807047,Human_RBP_ID_8643189,Human_RBP_ID_15793038 19583 RMVar_ID_19583 Human_SNP_ID_272562041 A-to-I Human chr6 - 33771354 33771354 33771354 CTCTCATTTCCTCTGATGTCTGGATGATCGGCAGGGCAGGAATCTGAGCGCTGGCCCCGTGGTGA CTCTCATTTCCTCTGATGTCTGGATGATCGGCGGGGCAGGAATCTGAGCGCTGGCCCCGTGGTGA T C LEMD2 Ensembl:ENSG00000161904 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs11545231 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_662716,Human_RBP_ID_792250,Human_RBP_ID_24158655 Human_miRNA_ID_865755 19584 RMVar_ID_19584 Human_SNP_ID_272690440 A-to-I Human chr6 + 34274645 34274645 34274645 AGCTGGGTGTGGTGGCATGTGCCTGTAATCCCAGCTACTCGCGAGGCTGAGGTAGGAGAACTGCT AGCTGGGTGTGGTGGCATGTGCCTGTAATCCCGGCTACTCGCGAGGCTGAGGTAGGAGAACTGCT A G AL354740.1 Ensembl:ENSG00000225339 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs567947504 Functional Loss SNV dbSNP153 33..33 33 - - - 19585 RMVar_ID_19585 Human_SNP_ID_272695229 A-to-I Human chr6 - 34294902 34294902 34294902 TGAGCAGATGCTGGGCGTGGTGGCTCACACCTATAATCCCAGCGTTTTGGGAAGCTGACACAGGA TGAGCAGATGCTGGGCGTGGTGGCTCACACCTGTAATCCCAGCGTTTTGGGAAGCTGACACAGGA T C RPS10-NUDT3,NUDT3 Ensembl:ENSG00000270800,Ensembl:ENSG00000272325 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs775210118 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_237947,RMVar_hsa_circ_237948,RMVar_hsa_circ_237950,RMVar_hsa_circ_320512,RMVar_hsa_circ_237946,RMVar_hsa_circ_302831,RMVar_hsa_circ_237949 19586 RMVar_ID_19586 Human_SNP_ID_272696237 A-to-I Human chr6 - 34298177 34298177 34298177 TTTTGTATTTTGTAGAGATGGGGTTTCACCTTATTGCCCAGGCTGGTCTCGAACTCTTGGGCTCA TTTTGTATTTTGTAGAGATGGGGTTTCACCTTGTTGCCCAGGCTGGTCTCGAACTCTTGGGCTCA T C RPS10-NUDT3,NUDT3 Ensembl:ENSG00000270800,Ensembl:ENSG00000272325 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1057487783 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1737,RMVar_hsa_circ_237947,RMVar_hsa_circ_237948,RMVar_hsa_circ_237950,RMVar_hsa_circ_320512 19587 RMVar_ID_19587 Human_SNP_ID_272701401 A-to-I Human chr6 - 34320651 34320651 34320651 TCTTGTATTTTTTGTAGAAATGGGGTTTCACCATGTTGACCGGGCTGGTCTCGAACTCCGGGCTC TCTTGTATTTTTTGTAGAAATGGGGTTTCACCGTGTTGACCGGGCTGGTCTCGAACTCCGGGCTC T C RPS10-NUDT3,NUDT3 Ensembl:ENSG00000270800,Ensembl:ENSG00000272325 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs948300526 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15795089,Human_RBP_ID_17576298,Human_RBP_ID_25999794 RMVar_hsa_circ_1737,RMVar_hsa_circ_237947,RMVar_hsa_circ_237948,RMVar_hsa_circ_237950,RMVar_hsa_circ_320512 19588 RMVar_ID_19588 Human_SNP_ID_272703436 A-to-I Human chr6 - 34328449 34328446 34328449 TCCGTTTTTTCATTCTACTAGGAACATGTATTATTTTTATAATCAGAAAAAAATGGTAAGCTATA TCCGTTTTTTCATTCTACTAGGAACATGTATT___TTTATAATCAGAAAAAAATGGTAAGCTATA AAAT A RPS10-NUDT3,NUDT3 Ensembl:ENSG00000270800,Ensembl:ENSG00000272325 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs770264374 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_1737,RMVar_hsa_circ_237947,RMVar_hsa_circ_237948,RMVar_hsa_circ_237950,RMVar_hsa_circ_320512 19589 RMVar_ID_19589 Human_SNP_ID_272709891 A-to-I Human chr6 - 34354611 34354611 34354611 TCAAGAAATTCTCCTGCCTCAACCTCCCAAGTAGTTGGAACTACAGGTGCCTGCCACCACGCCTG TCAAGAAATTCTCCTGCCTCAACCTCCCAAGTTGTTGGAACTACAGGTGCCTGCCACCACGCCTG T A RPS10-NUDT3,NUDT3 Ensembl:ENSG00000270800,Ensembl:ENSG00000272325 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1415613362 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_170623 RMVar_hsa_circ_237948,RMVar_hsa_circ_120917,RMVar_hsa_circ_237952 19590 RMVar_ID_19590 Human_SNP_ID_272715186 A-to-I Human chr6 - 34375430 34375430 34375430 ATTGTGGGCCTTCTGTGTATAAAGCAGCATGTAGACTCCACGGAGGATAAACTATGAGCAGGAGA ATTGTGGGCCTTCTGTGTATAAAGCAGCATGTGGACTCCACGGAGGATAAACTATGAGCAGGAGA T C RPS10-NUDT3,NUDT3 Ensembl:ENSG00000270800,Ensembl:ENSG00000272325 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs996701217 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7596126,Human_RBP_ID_15796659 RMVar_hsa_circ_120917,RMVar_hsa_circ_237952 19591 RMVar_ID_19591 Human_SNP_ID_272717019 A-to-I Human chr6 - 34382978 34382978 34382978 GGATTACAGGTGCCTGCCACCGCACCCAGCTAATTTTTGCAGTTTTAGTAGAGATAGGGGTTTCA GGATTACAGGTGCCTGCCACCGCACCCAGCTAGTTTTTGCAGTTTTAGTAGAGATAGGGGTTTCA T C RPS10-NUDT3,NUDT3 Ensembl:ENSG00000270800,Ensembl:ENSG00000272325 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1471227363 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15796991 RMVar_hsa_circ_120917,RMVar_hsa_circ_237952 19592 RMVar_ID_19592 Human_SNP_ID_272725941 A-to-I Human chr6 - 34415929 34415929 34415929 CCTTTAATCCCAGCACTTTGGGAGGGCAAGATAGGCGGATCACTTGAGTCCAGGAGTTAAAGACC CCTTTAATCCCAGCACTTTGGGAGGGCAAGATTGGCGGATCACTTGAGTCCAGGAGTTAAAGACC T A RPS10-NUDT3 Ensembl:ENSG00000270800 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs548113328 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15798123 RMVar_hsa_circ_120917,RMVar_hsa_circ_237952 19593 RMVar_ID_19593 Human_SNP_ID_272725943 A-to-I Human chr6 - 34415933 34415933 34415933 CACACCTTTAATCCCAGCACTTTGGGAGGGCAAGATAGGCGGATCACTTGAGTCCAGGAGTTAAA CACACCTTTAATCCCAGCACTTTGGGAGGGCAGGATAGGCGGATCACTTGAGTCCAGGAGTTAAA T C RPS10-NUDT3 Ensembl:ENSG00000270800 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1161917897 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15798123 RMVar_hsa_circ_120917,RMVar_hsa_circ_237952 19594 RMVar_ID_19594 Human_SNP_ID_272725944 A-to-I Human chr6 - 34415934 34415934 34415934 TCACACCTTTAATCCCAGCACTTTGGGAGGGCAAGATAGGCGGATCACTTGAGTCCAGGAGTTAA TCACACCTTTAATCCCAGCACTTTGGGAGGGCGAGATAGGCGGATCACTTGAGTCCAGGAGTTAA T C RPS10-NUDT3 Ensembl:ENSG00000270800 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs909858024 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15798123 RMVar_hsa_circ_120917,RMVar_hsa_circ_237952 19595 RMVar_ID_19595 Human_SNP_ID_272726666 A-to-I Human chr6 - 34418354 34418354 34418354 GCAACCGAATTCCAGTTTGTGAGTATCTTCCTATTTGTTTTCCATGAGCCATCACTTGTTCTGGC GCAACCGAATTCCAGTTTGTGAGTATCTTCCTGTTTGTTTTCCATGAGCCATCACTTGTTCTGGC T C RPS10,RPS10-NUDT3 Ensembl:ENSG00000124614,Ensembl:ENSG00000270800 Protein coding,Protein coding intron,intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs770796118 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_949450,Human_RBP_ID_2019563,Human_RBP_ID_3004352,Human_RBP_ID_5400650,Human_RBP_ID_7596643,Human_RBP_ID_15798247,Human_RBP_ID_19130852,Human_RBP_ID_22684059,Human_RBP_ID_24435708 Human_Splice_Rec_763364,Human_Splice_Rec_763380,Human_Splice_Rec_763394,Human_Splice_Rec_763414,Human_Splice_Rec_763424,Human_Splice_Rec_763434,Human_Splice_Rec_763444,Human_Splice_Rec_763456,Human_Splice_Rec_763464,Human_Splice_Rec_763474 RMVar_hsa_circ_105007,RMVar_hsa_circ_120917,RMVar_hsa_circ_237952,RMVar_hsa_circ_100712,RMVar_hsa_circ_237954,RMVar_hsa_circ_237955 19596 RMVar_ID_19596 Human_SNP_ID_272727209 A-to-I Human chr6 - 34420198 34420198 34420198 AAAAGAAAACGATTACTGAAACCATATTCGTTATTGGCATTTGCTTTCCTCCCCCTATTCTTGTA AAAAGAAAACGATTACTGAAACCATATTCGTTGTTGGCATTTGCTTTCCTCCCCCTATTCTTGTA T C RPS10,RPS10-NUDT3 Ensembl:ENSG00000124614,Ensembl:ENSG00000270800 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs755585428 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3004360 RMVar_hsa_circ_105007,RMVar_hsa_circ_120917,RMVar_hsa_circ_237952,RMVar_hsa_circ_100712,RMVar_hsa_circ_237954,RMVar_hsa_circ_237955 19597 RMVar_ID_19597 Human_SNP_ID_272727526 A-to-I Human chr6 - 34421218 34421218 34421218 GATCATGCCATTGTATTAGATCTATGGCTCACACTGGGCACGAGGATAGGGGGAGGAAAGCAAAT GATCATGCCATTGTATTAGATCTATGGCTCACGCTGGGCACGAGGATAGGGGGAGGAAAGCAAAT T C RPS10,RPS10-NUDT3 Ensembl:ENSG00000124614,Ensembl:ENSG00000270800 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1160263705 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3004365,Human_RBP_ID_8643527,Human_RBP_ID_15798352,Human_RBP_ID_22728364 RMVar_hsa_circ_105007,RMVar_hsa_circ_120917,RMVar_hsa_circ_237952,RMVar_hsa_circ_100712,RMVar_hsa_circ_237954,RMVar_hsa_circ_237955 19598 RMVar_ID_19598 Human_SNP_ID_272727546 A-to-I Human chr6 - 34421289 34421289 34421289 GTCCCAGCTACTTAGGAGGCTGAGGCATGAGAATTGCTTGAACCTGGGAGGCAGAGGCCGCAGTG GTCCCAGCTACTTAGGAGGCTGAGGCATGAGACTTGCTTGAACCTGGGAGGCAGAGGCCGCAGTG T G RPS10,RPS10-NUDT3 Ensembl:ENSG00000124614,Ensembl:ENSG00000270800 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1183324963 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105007,RMVar_hsa_circ_120917,RMVar_hsa_circ_237952,RMVar_hsa_circ_100712,RMVar_hsa_circ_237954,RMVar_hsa_circ_237955 19599 RMVar_ID_19599 Human_SNP_ID_272727549 A-to-I Human chr6 - 34421308 34421308 34421308 GTGGTGGTGGGCGTCTGTAGTCCCAGCTACTTAGGAGGCTGAGGCATGAGAATTGCTTGAACCTG GTGGTGGTGGGCGTCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCATGAGAATTGCTTGAACCTG T C RPS10,RPS10-NUDT3 Ensembl:ENSG00000124614,Ensembl:ENSG00000270800 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1325749360 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26000063 RMVar_hsa_circ_105007,RMVar_hsa_circ_120917,RMVar_hsa_circ_237952,RMVar_hsa_circ_100712,RMVar_hsa_circ_237954,RMVar_hsa_circ_237955 19600 RMVar_ID_19600 Human_SNP_ID_272727577 A-to-I Human chr6 - 34421387 34421387 34421387 TTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGACGAAACCCTGTCTCTATTAAAAATACA TTGAGGTCAGGAGTTCGAGACCAGCCTGGCCACCATGACGAAACCCTGTCTCTATTAAAAATACA T G RPS10,RPS10-NUDT3 Ensembl:ENSG00000124614,Ensembl:ENSG00000270800 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs887213563 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105007,RMVar_hsa_circ_120917,RMVar_hsa_circ_237952,RMVar_hsa_circ_100712,RMVar_hsa_circ_237954,RMVar_hsa_circ_237955 19601 RMVar_ID_19601 Human_SNP_ID_272727931 A-to-I Human chr6 - 34422590 34422590 34422590 AAAAATTAGCCTGGGCGTGGTGGCTCGTGCCTATAATCCCATCACTTTGGAAGGCCAAGGCGGGA AAAAATTAGCCTGGGCGTGGTGGCTCGTGCCTGTAATCCCATCACTTTGGAAGGCCAAGGCGGGA T C RPS10,RPS10-NUDT3 Ensembl:ENSG00000124614,Ensembl:ENSG00000270800 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1338533853 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10281027,Human_RBP_ID_17576302 RMVar_hsa_circ_105007,RMVar_hsa_circ_237955,RMVar_hsa_circ_93224,RMVar_hsa_circ_237956 19602 RMVar_ID_19602 Human_SNP_ID_272727969 A-to-I Human chr6 - 34422731 34422731 34422731 TGTGCCTTAGGGTGTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGAGGA TGTGCCTTAGGGTGTGGTGGCTCACACCTGTACTCCCAGCACTTTGGGAGGCCAAGGCGGGAGGA T G RPS10,RPS10-NUDT3 Ensembl:ENSG00000124614,Ensembl:ENSG00000270800 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1315381570 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15798407,Human_RBP_ID_17576660 RMVar_hsa_circ_105007,RMVar_hsa_circ_237955,RMVar_hsa_circ_93224,RMVar_hsa_circ_237956 19603 RMVar_ID_19603 Human_SNP_ID_272727975 A-to-I Human chr6 - 34422738 34422738 34422738 TAAAGTTTGTGCCTTAGGGTGTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGC TAAAGTTTGTGCCTTAGGGTGTGGTGGCTCACCCCTGTAATCCCAGCACTTTGGGAGGCCAAGGC T G RPS10,RPS10-NUDT3 Ensembl:ENSG00000124614,Ensembl:ENSG00000270800 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005041041 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17576660 RMVar_hsa_circ_105007,RMVar_hsa_circ_237955,RMVar_hsa_circ_93224,RMVar_hsa_circ_237956 19604 RMVar_ID_19604 Human_SNP_ID_272728015 A-to-I Human chr6 - 34422889 34422889 34422889 TTTAGTAGAGACAGGGTTTTACCATGTTGGCCAGGTTGTTCTTGAACTCCTGGCCTCAAGTGATC TTTAGTAGAGACAGGGTTTTACCATGTTGGCCGGGTTGTTCTTGAACTCCTGGCCTCAAGTGATC T C RPS10,RPS10-NUDT3 Ensembl:ENSG00000124614,Ensembl:ENSG00000270800 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1042276479 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15798411 RMVar_hsa_circ_105007,RMVar_hsa_circ_237955,RMVar_hsa_circ_93224,RMVar_hsa_circ_237956 19605 RMVar_ID_19605 Human_SNP_ID_272767926 A-to-I Human chr6 - 34579313 34579313 34579313 AAATTAGCTGAGCGTGATGGCACGCGCCTGTAATTCCAGCTACTCGGGAGTCTGAGGCAGGAGAA AAATTAGCTGAGCGTGATGGCACGCGCCTGTACTTCCAGCTACTCGGGAGTCTGAGGCAGGAGAA T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1213906644 Functional Loss SNV dbSNP153 33..33 33 - - - 19606 RMVar_ID_19606 Human_SNP_ID_272768680 A-to-I Human chr6 - 34582091 34582091 34582091 TGACTCAAGCAATCCTCCCACATCAGTCTCCAAAGTAACTGGGACCACAGGCACACTCCACTACG TGACTCAAGCAATCCTCCCACATCAGTCTCCAGAGTAACTGGGACCACAGGCACACTCCACTACG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1449186605 Functional Loss SNV dbSNP153 33..33 33 - - - 19607 RMVar_ID_19607 Human_SNP_ID_272770787 A-to-I Human chr6 - 34591412 34591412 34591412 GGACTTATTGCAGCTTCGACCTTCCAGGTTCAAGTGATCGTCCCACTTCAGCCTCCCAAGTAGCT GGACTTATTGCAGCTTCGACCTTCCAGGTTCAGGTGATCGTCCCACTTCAGCCTCCCAAGTAGCT T C ILRUN Ensembl:ENSG00000196821 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs772778306 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1217529 RMVar_hsa_circ_79574,RMVar_hsa_circ_82446,RMVar_hsa_circ_237959,RMVar_hsa_circ_237960 19608 RMVar_ID_19608 Human_SNP_ID_272777486 A-to-I Human chr6 - 34619479 34619479 34619479 GGCAAGTGCCTGCGTGTAGTCCCAGCTACTCAAGAGGTTGAGGGGGGAGGATCACTTGAGCCCAG GGCAAGTGCCTGCGTGTAGTCCCAGCTACTCAGGAGGTTGAGGGGGGAGGATCACTTGAGCCCAG T C ILRUN Ensembl:ENSG00000196821 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1316585297 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79574,RMVar_hsa_circ_82446,RMVar_hsa_circ_237959,RMVar_hsa_circ_237960,RMVar_hsa_circ_237963,RMVar_hsa_circ_359792,RMVar_hsa_circ_271098,RMVar_hsa_circ_237962 19609 RMVar_ID_19609 Human_SNP_ID_272779864 A-to-I Human chr6 - 34629057 34629057 34629057 CTCTGTTGCCCAGGCTGGTATGCAGTGATCTCAGGTCACTGCAACCTCTGTCTCCCAGGCACAAA CTCTGTTGCCCAGGCTGGTATGCAGTGATCTCGGGTCACTGCAACCTCTGTCTCCCAGGCACAAA T C ILRUN Ensembl:ENSG00000196821 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1015722214 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79574,RMVar_hsa_circ_82446,RMVar_hsa_circ_237959,RMVar_hsa_circ_237960,RMVar_hsa_circ_237963,RMVar_hsa_circ_359792,RMVar_hsa_circ_271098,RMVar_hsa_circ_237962 19610 RMVar_ID_19610 Human_SNP_ID_272785584 A-to-I Human chr6 - 34652899 34652899 34652899 CTCCCACCTTGGCATTCTAAAATGCTGGGATTACAGGCATGAACCACTGCACCTGGCCTTAAATT CTCCCACCTTGGCATTCTAAAATGCTGGGATTGCAGGCATGAACCACTGCACCTGGCCTTAAATT T C ILRUN Ensembl:ENSG00000196821 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1485753101 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79574,RMVar_hsa_circ_82446,RMVar_hsa_circ_237959,RMVar_hsa_circ_237960,RMVar_hsa_circ_237963,RMVar_hsa_circ_359792,RMVar_hsa_circ_304065,RMVar_hsa_circ_237966 19611 RMVar_ID_19611 Human_SNP_ID_272787440 A-to-I Human chr6 - 34660105 34660104 34660105 AAGGGATGAGGTTTCGCCATGTTACCTAGGCTAGTCTCAAACTTCTGGGCTGAAGTGATCCACCT AAGGGATGAGGTTTCGCCATGTTACCTAGGCT_GTCTCAAACTTCTGGGCTGAAGTGATCCACCT CT C ILRUN Ensembl:ENSG00000196821 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1282438921 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_82446,RMVar_hsa_circ_237960 19612 RMVar_ID_19612 Human_SNP_ID_272793246 A-to-I Human chr6 - 34682612 34682589 34682613 AAAATTAGCTGGGCATGGTGGCGTGCACTTGTAGTCCCAGCTACTTGGGAGGCTGAGATGAGAGG AAAATTAGCTGGGCATGGTGGCGTGCACTTG________________________AGATGAGAGG TCAGCCTCCCAAGTAGCTGGGACTA T ILRUN Ensembl:ENSG00000196821 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1304730711 Functional Loss DEL dbSNP153 32..55 33 - - - RMVar_hsa_circ_82446,RMVar_hsa_circ_237960 19613 RMVar_ID_19613 Human_SNP_ID_272795320 A-to-I Human chr6 - 34688885 34688885 34688885 GTGATCTTGGCTCGCTGTAACCTCCGCCTCCCAGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCG GTGATCTTGGCTCGCTGTAACCTCCGCCTCCCGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCG T C ILRUN Ensembl:ENSG00000196821 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs951484021 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24159381 RMVar_hsa_circ_82446,RMVar_hsa_circ_237960 19614 RMVar_ID_19614 Human_SNP_ID_272796092 A-to-I Human chr6 - 34692167 34692167 34692167 TTGAACCCAGGAGTTTGAGACCAGCATAGGCAAGATAGCGAGACCTCCATCTCTACAAAAATAAA TTGAACCCAGGAGTTTGAGACCAGCATAGGCAGGATAGCGAGACCTCCATCTCTACAAAAATAAA T C ILRUN Ensembl:ENSG00000196821 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs746885012 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82446,RMVar_hsa_circ_237960 19615 RMVar_ID_19615 Human_SNP_ID_272796100 A-to-I Human chr6 - 34692215 34692215 34692215 TCACGCCTATAATCCCAGCACTTTGGGAGGCCAGGGCAGTAGGATTGCTTGAACCCAGGAGTTTG TCACGCCTATAATCCCAGCACTTTGGGAGGCCGGGGCAGTAGGATTGCTTGAACCCAGGAGTTTG T C ILRUN Ensembl:ENSG00000196821 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879164873 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82446,RMVar_hsa_circ_237960 19616 RMVar_ID_19616 Human_SNP_ID_272796211 A-to-I Human chr6 - 34692731 34692731 34692731 TTAGAGATGGGTCGCACTATGTTGCCAGACCTAGTCTTGAACTCTTGGGCTCAATCTTGCCTTAG TTAGAGATGGGTCGCACTATGTTGCCAGACCTTGTCTTGAACTCTTGGGCTCAATCTTGCCTTAG T A ILRUN Ensembl:ENSG00000196821 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs927661582 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15800042 RMVar_hsa_circ_82446,RMVar_hsa_circ_237960 19617 RMVar_ID_19617 Human_SNP_ID_272796216 A-to-I Human chr6 - 34692745 34692745 34692745 ATTTAAACATTTTTTTAGAGATGGGTCGCACTATGTTGCCAGACCTAGTCTTGAACTCTTGGGCT ATTTAAACATTTTTTTAGAGATGGGTCGCACTGTGTTGCCAGACCTAGTCTTGAACTCTTGGGCT T C ILRUN Ensembl:ENSG00000196821 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs919259491 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7597205,Human_RBP_ID_15800043 RMVar_hsa_circ_82446,RMVar_hsa_circ_237960 19618 RMVar_ID_19618 Human_SNP_ID_272796286 A-to-I Human chr6 - 34693018 34693018 34693018 GCTGAAGTGCAGTGGCACAGCTGTGGCTCACTACAGCCTCAACCTCCCAGATTCAAGCAATCCTC GCTGAAGTGCAGTGGCACAGCTGTGGCTCACTGCAGCCTCAACCTCCCAGATTCAAGCAATCCTC T C ILRUN Ensembl:ENSG00000196821 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1230211577 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82446,RMVar_hsa_circ_237960 19619 RMVar_ID_19619 Human_SNP_ID_272796589 A-to-I Human chr6 - 34693957 34693957 34693957 GAAATGAGTCGGGCTTAATGGTATGCACCTGTAGTACCAGCTACTTGGGAGGCTGAAGTGGGAGG GAAATGAGTCGGGCTTAATGGTATGCACCTGTGGTACCAGCTACTTGGGAGGCTGAAGTGGGAGG T C ILRUN Ensembl:ENSG00000196821 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1357416931 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82446,RMVar_hsa_circ_237960 19620 RMVar_ID_19620 Human_SNP_ID_272802692 A-to-I Human chr6 - 34718139 34718139 34718139 AAAATTAGCCGGGCTTGGTGGTGGATGCCTGTAATCCCAGCTACTCTGGAGGCTGAGGCAGGAAA AAAATTAGCCGGGCTTGGTGGTGGATGCCTGTGATCCCAGCTACTCTGGAGGCTGAGGCAGGAAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1271257091 Functional Loss SNV dbSNP153 33..33 33 - - - 19621 RMVar_ID_19621 Human_SNP_ID_272813012 A-to-I Human chr6 + 34760212 34760212 34760212 TTGTTTCACTGCAGCCTCTGCGTCCCAGGCTCAAGCAATTCTCCTGTCTCAGCTTCTCCAGTAGC TTGTTTCACTGCAGCCTCTGCGTCCCAGGCTCGAGCAATTCTCCTGTCTCAGCTTCTCCAGTAGC A G SNRPC Ensembl:ENSG00000124562 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs892649161 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47598 19622 RMVar_ID_19622 Human_SNP_ID_272814478 A-to-I Human chr6 + 34765950 34765950 34765950 TTTTATAGAGATGGTGTCTCACTTTGTTGCCCAGGCTGGTCTTGAACTCCTGGCCTCAAGCAATC TTTTATAGAGATGGTGTCTCACTTTGTTGCCCGGGCTGGTCTTGAACTCCTGGCCTCAAGCAATC A G SNRPC Ensembl:ENSG00000124562 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1419018197 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47598,RMVar_hsa_circ_237968,RMVar_hsa_circ_85729,RMVar_hsa_circ_342383 19623 RMVar_ID_19623 Human_SNP_ID_272826863 A-to-I Human chr6 + 34816474 34816474 34816474 TCTACAAAAAATAAAAAAAATTAGCTGGGTATAGTGACATGCACTTGTGGTTCTAGCTACTCTGG TCTACAAAAAATAAAAAAAATTAGCTGGGTATGGTGACATGCACTTGTGGTTCTAGCTACTCTGG A G UHRF1BP1 Ensembl:ENSG00000065060 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs187967870 Functional Loss SNV dbSNP153 33..33 33 - - - 19624 RMVar_ID_19624 Human_SNP_ID_272828751 A-to-I Human chr6 + 34824017 34824017 34824017 CAGCCTGGAGTGCAGTGGTGTGATCTTGGCTCACTGCATCATCTGCCTCCCAGGCTCAAGTGGTT CAGCCTGGAGTGCAGTGGTGTGATCTTGGCTCGCTGCATCATCTGCCTCCCAGGCTCAAGTGGTT A G UHRF1BP1 Ensembl:ENSG00000065060 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1304808807 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_237970,RMVar_hsa_circ_345769,RMVar_hsa_circ_351364,RMVar_hsa_circ_283008,RMVar_hsa_circ_237971,RMVar_hsa_circ_237975,RMVar_hsa_circ_237969,RMVar_hsa_circ_372227,RMVar_hsa_circ_266063 19625 RMVar_ID_19625 Human_SNP_ID_272837872 A-to-I Human chr6 + 34862579 34862579 34862579 CATAGTGGCTGGGCGCGGTGGCTCACGCCTGTAATCCCGGCACTTTGGAAGGCTGAGGCAGGCAG CATAGTGGCTGGGCGCGGTGGCTCACGCCTGTTATCCCGGCACTTTGGAAGGCTGAGGCAGGCAG A T UHRF1BP1 Ensembl:ENSG00000065060 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1244907892 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77370,RMVar_hsa_circ_266063,RMVar_hsa_circ_267607,RMVar_hsa_circ_370878,RMVar_hsa_circ_108479,RMVar_hsa_circ_237979,RMVar_hsa_circ_71476,RMVar_hsa_circ_237980,RMVar_hsa_circ_237978,RMVar_hsa_circ_378155,RMVar_hsa_circ_237984,RMVar_hsa_circ_93372,RMVar_hsa_circ_109584,RMVar_hsa_circ_237985 19626 RMVar_ID_19626 Human_SNP_ID_272838004 A-to-I Human chr6 + 34863107 34863107 34863107 TTTGTATTTTTTTGTAGAGACCAGGTTTTGCCATGTTGCCCAGGCTGGTCTCGAACTCCTGGATT TTTGTATTTTTTTGTAGAGACCAGGTTTTGCCCTGTTGCCCAGGCTGGTCTCGAACTCCTGGATT A C UHRF1BP1 Ensembl:ENSG00000065060 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs556159020 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77370,RMVar_hsa_circ_266063,RMVar_hsa_circ_267607,RMVar_hsa_circ_370878,RMVar_hsa_circ_108479,RMVar_hsa_circ_237979,RMVar_hsa_circ_71476,RMVar_hsa_circ_237980,RMVar_hsa_circ_237978,RMVar_hsa_circ_378155,RMVar_hsa_circ_237984,RMVar_hsa_circ_93372,RMVar_hsa_circ_109584,RMVar_hsa_circ_237985 19627 RMVar_ID_19627 Human_SNP_ID_272838005 A-to-I Human chr6 + 34863107 34863107 34863107 TTTGTATTTTTTTGTAGAGACCAGGTTTTGCCATGTTGCCCAGGCTGGTCTCGAACTCCTGGATT TTTGTATTTTTTTGTAGAGACCAGGTTTTGCCTTGTTGCCCAGGCTGGTCTCGAACTCCTGGATT A T UHRF1BP1 Ensembl:ENSG00000065060 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs556159020 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77370,RMVar_hsa_circ_266063,RMVar_hsa_circ_267607,RMVar_hsa_circ_370878,RMVar_hsa_circ_108479,RMVar_hsa_circ_237979,RMVar_hsa_circ_71476,RMVar_hsa_circ_237980,RMVar_hsa_circ_237978,RMVar_hsa_circ_378155,RMVar_hsa_circ_237984,RMVar_hsa_circ_93372,RMVar_hsa_circ_109584,RMVar_hsa_circ_237985 19628 RMVar_ID_19628 Human_SNP_ID_272839319 A-to-I Human chr6 - 34868688 34868688 34868688 ACAGAGTCTTGCTCTGTCACCCAGGCTGTAGTACAAGGGCGCGATCTCGGCTCACTGCAACCTCC ACAGAGTCTTGCTCTGTCACCCAGGCTGTAGTGCAAGGGCGCGATCTCGGCTCACTGCAACCTCC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1406811145 Functional Loss SNV dbSNP153 33..33 33 - - - 19629 RMVar_ID_19629 Human_SNP_ID_272842372 A-to-I Human chr6 - 34882393 34882393 34882393 GTGATCTGCCCGCCTCGGCCTCCCAAAGTGCTAGGATTACAGGCATGAGCCACTGTGCCCGGCCT GTGATCTGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGTGCCCGGCCT T C TAF11 Ensembl:ENSG00000064995 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1272387890 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123280,RMVar_hsa_circ_89116,RMVar_hsa_circ_237991,RMVar_hsa_circ_237992 19630 RMVar_ID_19630 Human_SNP_ID_272846809 A-to-I Human chr6 + 34901614 34901614 34901614 CTCATTGTAACTTCAGCCTCCTGGGCTCAAGCAATCTTCCCACCTGAGTCTACTGAGTAGCTGGG CTCATTGTAACTTCAGCCTCCTGGGCTCAAGCCATCTTCCCACCTGAGTCTACTGAGTAGCTGGG A C ANKS1A Ensembl:ENSG00000064999 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1486339876 Functional Loss SNV dbSNP153 33..33 33 - - - 19631 RMVar_ID_19631 Human_SNP_ID_272863526 A-to-I Human chr6 + 34978148 34978148 34978148 ACCCAGCTAATTTTTGTATTTTTGGTGGAGACAGGGTTTCACTGTGTTGTCCAGGGGGTCTCTAT ACCCAGCTAATTTTTGTATTTTTGGTGGAGACGGGGTTTCACTGTGTTGTCCAGGGGGTCTCTAT A G ANKS1A Ensembl:ENSG00000064999 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1164761921 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_237993,RMVar_hsa_circ_119774,RMVar_hsa_circ_326142,RMVar_hsa_circ_377188,RMVar_hsa_circ_237994 19632 RMVar_ID_19632 Human_SNP_ID_272885385 A-to-I Human chr6 + 35076152 35076152 35076152 TTCATAGAAAAACTCTGAGGCTGTCCGGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGG TTCATAGAAAAACTCTGAGGCTGTCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG A G ANKS1A Ensembl:ENSG00000064999 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs545952251 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103723,RMVar_hsa_circ_237993,RMVar_hsa_circ_119774,RMVar_hsa_circ_237999,RMVar_hsa_circ_363866,RMVar_hsa_circ_326596,RMVar_hsa_circ_363281,RMVar_hsa_circ_238005,RMVar_hsa_circ_47387,RMVar_hsa_circ_267960 19633 RMVar_ID_19633 Human_SNP_ID_272904717 A-to-I Human chr6 - 35159112 35159112 35159112 AGAATACAGTGGCATGATCTCGGTTCACTGCAACCTCCGCCTTCCGCATTCAAGCAATTCTCCTC AGAATACAGTGGCATGATCTCGGTTCACTGCACCCTCCGCCTTCCGCATTCAAGCAATTCTCCTC T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs929689810 Functional Loss SNV dbSNP153 33..33 33 - - - 19634 RMVar_ID_19634 Human_SNP_ID_272920299 A-to-I Human chr6 - 35229240 35229240 35229240 GACTAATTTTTATTATTATTATTTTTTGTAGAAACAGGGTCTCACTATGTTGCCCAGGCCTGTCT GACTAATTTTTATTATTATTATTTTTTGTAGATACAGGGTCTCACTATGTTGCCCAGGCCTGTCT T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1473358993 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15803587 19635 RMVar_ID_19635 Human_SNP_ID_272930773 A-to-I Human chr6 + 35273521 35273521 35273521 AGCCCAAGTCAGGGCCAGGCACAATGGCTCACACCTATAATCCCAGTACATTGGGAGGCCAACGC AGCCCAAGTCAGGGCCAGGCACAATGGCTCACGCCTATAATCCCAGTACATTGGGAGGCCAACGC A G ZNF76 Ensembl:ENSG00000065029 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1013907696 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89150,RMVar_hsa_circ_238018 19636 RMVar_ID_19636 Human_SNP_ID_272932470 A-to-I Human chr6 + 35280263 35280263 35280263 ATGAATGTTAGAACATGAGTTGGAAGAGGCTGAGGCAGGAAGATCACTTGAGCCCAGGAGTTCGA ATGAATGTTAGAACATGAGTTGGAAGAGGCTGCGGCAGGAAGATCACTTGAGCCCAGGAGTTCGA A C ZNF76 Ensembl:ENSG00000065029 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559432528 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89150,RMVar_hsa_circ_238018 19637 RMVar_ID_19637 Human_SNP_ID_272937757 A-to-I Human chr6 + 35300058 35300058 35300058 TTGTTGTTGTTTTAGAGATGAGATCTTGTTCTATCACTCATGCTGGAGTGCAGTGGTGCAGTCAT TTGTTGTTGTTTTAGAGATGAGATCTTGTTCTGTCACTCATGCTGGAGTGCAGTGGTGCAGTCAT A G DEF6 Ensembl:ENSG00000023892 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs563132099 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110847,RMVar_hsa_circ_238039,RMVar_hsa_circ_93192,RMVar_hsa_circ_238040 19638 RMVar_ID_19638 Human_SNP_ID_272937889 A-to-I Human chr6 + 35300633 35300633 35300633 CTTTGAATTCTTGTAGAAAGTACAATGGCTTCATCCAGTTGGGTTGAGAACAGAGAAAGTAAACC CTTTGAATTCTTGTAGAAAGTACAATGGCTTCGTCCAGTTGGGTTGAGAACAGAGAAAGTAAACC A G DEF6 Ensembl:ENSG00000023892 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1888823 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_1679,GWAS_ID_1680,GWAS_ID_1681,GWAS_ID_1682,GWAS_ID_1683,GWAS_ID_1684 RMVar_hsa_circ_110847,RMVar_hsa_circ_238039,RMVar_hsa_circ_93192,RMVar_hsa_circ_238040 19639 RMVar_ID_19639 Human_SNP_ID_272938625 A-to-I Human chr6 + 35304200 35304200 35304200 AAAATTAGCCGGGTGTGATGGCGCACGCCTACAGTTCCAGCTACTCAGGAGGCTGATATGGGAAG AAAATTAGCCGGGTGTGATGGCGCACGCCTACGGTTCCAGCTACTCAGGAGGCTGATATGGGAAG A G DEF6 Ensembl:ENSG00000023892 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs117311433 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110847,RMVar_hsa_circ_238039,RMVar_hsa_circ_93192,RMVar_hsa_circ_238040 19640 RMVar_ID_19640 Human_SNP_ID_272938789 A-to-I Human chr6 + 35305075 35305075 35305075 GGAGGGCTCTTCCTGCCTCGGCCTCCTAAAGCATTGGGATTACAGGTATGAGCCACCATGGCCTG GGAGGGCTCTTCCTGCCTCGGCCTCCTAAAGCGTTGGGATTACAGGTATGAGCCACCATGGCCTG A G DEF6 Ensembl:ENSG00000023892 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1336115462 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110847,RMVar_hsa_circ_238039,RMVar_hsa_circ_93192,RMVar_hsa_circ_238040 19641 RMVar_ID_19641 Human_SNP_ID_272938923 A-to-I Human chr6 + 35305601 35305597 35305601 TGTGTGTGTATGTGTGTGTGTGACAGAGTCTCACTCTGCCACCCAGGCTGGAGTGCAGTGGCACT TGTGTGTGTATGTGTGTGTGTGACAGAGT____CTCTGCCACCCAGGCTGGAGTGCAGTGGCACT TCTCA T DEF6 Ensembl:ENSG00000023892 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs550400478 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_110847,RMVar_hsa_circ_238039,RMVar_hsa_circ_93192,RMVar_hsa_circ_238040 19642 RMVar_ID_19642 Human_SNP_ID_272965600 A-to-I Human chr6 + 35418264 35418264 35418264 GAAACCCTGCCTGCCCCAGCATCTGCACAGGCATCCACAAAGGGTTTCTGTCATGTTATCTCTTT GAAACCCTGCCTGCCCCAGCATCTGCACAGGCGTCCACAAAGGGTTTCTGTCATGTTATCTCTTT A G PPARD Ensembl:ENSG00000112033 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs9462082 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_1685,GWAS_ID_1686,GWAS_ID_1687,GWAS_ID_1688,GWAS_ID_1689,GWAS_ID_1690,GWAS_ID_1691,GWAS_ID_1692,GWAS_ID_1693,GWAS_ID_1694,GWAS_ID_1695,GWAS_ID_1696,GWAS_ID_1697,GWAS_ID_1698,GWAS_ID_1699,GWAS_ID_1700,GWAS_ID_1701,GWAS_ID_1702,GWAS_ID_1703,GWAS_ID_1704,GWAS_ID_1705,GWAS_ID_1706,GWAS_ID_1707,GWAS_ID_1708,GWAS_ID_1709,GWAS_ID_1710,GWAS_ID_1711,GWAS_ID_1712,GWAS_ID_1713,GWAS_ID_1714,GWAS_ID_1715,GWAS_ID_1716,GWAS_ID_1717,GWAS_ID_1718,GWAS_ID_1719,GWAS_ID_1720,GWAS_ID_1721,GWAS_ID_1722,GWAS_ID_1723,GWAS_ID_1724,GWAS_ID_1725 19643 RMVar_ID_19643 Human_SNP_ID_272982481 A-to-I Human chr6 - 35482677 35482677 35482677 GAACTTTTGGCCTCAAGCAGTCCTCCCGCCTCAGCCTCCCAAAGTGCTAGGATTACGGGCACGAG GAACTTTTGGCCTCAAGCAGTCCTCCCGCCTCTGCCTCCCAAAGTGCTAGGATTACGGGCACGAG T A TEAD3 Ensembl:ENSG00000007866 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404626268 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15852,RMVar_hsa_circ_125422,RMVar_hsa_circ_85049,RMVar_hsa_circ_238068,RMVar_hsa_circ_13364,RMVar_hsa_circ_238069 19644 RMVar_ID_19644 Human_SNP_ID_273069346 A-to-I Human chr6 - 35836749 35836747 35836749 ATTATTATTATTATTATTATTATTATTGAGACAGGGTATCACTCTGTCACCCAGGCTGGAGTACA ATTATTATTATTATTATTATTATTATTGAGAC__GGTATCACTCTGTCACCCAGGCTGGAGTACA CCT C SRPK1 Ensembl:ENSG00000096063 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1163538327 Functional Loss DEL dbSNP153 33..34 33 - - - 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 19645 RMVar_ID_19645 Human_SNP_ID_273070188 A-to-I Human chr6 - 35839804 35839804 35839804 CTGGTGGTATGCACCTGTAATCCCAGCTACTCAGGAGGCTGAGACACAAGAATCACTGGAACCCA CTGGTGGTATGCACCTGTAATCCCAGCTACTCGGGAGGCTGAGACACAAGAATCACTGGAACCCA T C SRPK1 Ensembl:ENSG00000096063 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1435343157 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15805769 RMVar_hsa_circ_103457,RMVar_hsa_circ_123766,RMVar_hsa_circ_118747,RMVar_hsa_circ_7460,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_109295,RMVar_hsa_circ_238089,RMVar_hsa_circ_238084,RMVar_hsa_circ_310257,RMVar_hsa_circ_64111,RMVar_hsa_circ_238090 19646 RMVar_ID_19646 Human_SNP_ID_273070190 A-to-I Human chr6 - 35839808 35839808 35839808 GGACCTGGTGGTATGCACCTGTAATCCCAGCTACTCAGGAGGCTGAGACACAAGAATCACTGGAA GGACCTGGTGGTATGCACCTGTAATCCCAGCTCCTCAGGAGGCTGAGACACAAGAATCACTGGAA T G SRPK1 Ensembl:ENSG00000096063 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1394243492 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103457,RMVar_hsa_circ_123766,RMVar_hsa_circ_118747,RMVar_hsa_circ_7460,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_109295,RMVar_hsa_circ_238089,RMVar_hsa_circ_238084,RMVar_hsa_circ_310257,RMVar_hsa_circ_64111,RMVar_hsa_circ_238090 19647 RMVar_ID_19647 Human_SNP_ID_273071119 A-to-I Human chr6 - 35843624 35843624 35843624 CAACATGGTAAAACCCCATCTCTACTAAAAATACAAAAATTAGCTGGGCGTGGTGGCATGCACCT CAACATGGTAAAACCCCATCTCTACTAAAAATTCAAAAATTAGCTGGGCGTGGTGGCATGCACCT T A SRPK1 Ensembl:ENSG00000096063 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1489655892 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123766,RMVar_hsa_circ_118747,RMVar_hsa_circ_238091,RMVar_hsa_circ_7460,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_109295,RMVar_hsa_circ_238089,RMVar_hsa_circ_310257,RMVar_hsa_circ_64111,RMVar_hsa_circ_75743,RMVar_hsa_circ_295306,RMVar_hsa_circ_302899,RMVar_hsa_circ_238090,RMVar_hsa_circ_303105,RMVar_hsa_circ_301794,RMVar_hsa_circ_126735,RMVar_hsa_circ_267006,RMVar_hsa_circ_124581,RMVar_hsa_circ_238093,RMVar_hsa_circ_238094,RMVar_hsa_circ_238095,RMVar_hsa_circ_238092 19648 RMVar_ID_19648 Human_SNP_ID_273073171 A-to-I Human chr6 - 35853010 35853010 35853010 GTCTCAAACTCCTAGCTTCAAACGATCATCCTACCTCAGCCTCCCAAAGCACTGGAATTACAGGC GTCTCAAACTCCTAGCTTCAAACGATCATCCTGCCTCAGCCTCCCAAAGCACTGGAATTACAGGC T C SRPK1 Ensembl:ENSG00000096063 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs540294659 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15806353,Human_RBP_ID_23061387 RMVar_hsa_circ_123766,RMVar_hsa_circ_118747,RMVar_hsa_circ_238091,RMVar_hsa_circ_7460,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_109295,RMVar_hsa_circ_238089,RMVar_hsa_circ_310257,RMVar_hsa_circ_64111,RMVar_hsa_circ_75743,RMVar_hsa_circ_295306,RMVar_hsa_circ_302899,RMVar_hsa_circ_238090,RMVar_hsa_circ_303105,RMVar_hsa_circ_301794,RMVar_hsa_circ_126735,RMVar_hsa_circ_267006,RMVar_hsa_circ_124581,RMVar_hsa_circ_238093,RMVar_hsa_circ_238094,RMVar_hsa_circ_238095,RMVar_hsa_circ_238092 19649 RMVar_ID_19649 Human_SNP_ID_273073440 A-to-I Human chr6 - 35854036 35854036 35854036 TGAGACACAAGAATTGTTTGAACCTGGGAGGCAGAGGCTGCAGTGAGCTGAGATCACACCACTGC TGAGACACAAGAATTGTTTGAACCTGGGAGGCGGAGGCTGCAGTGAGCTGAGATCACACCACTGC T C SRPK1 Ensembl:ENSG00000096063 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1212237123 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15806397 RMVar_hsa_circ_123766,RMVar_hsa_circ_118747,RMVar_hsa_circ_238091,RMVar_hsa_circ_7460,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_109295,RMVar_hsa_circ_238089,RMVar_hsa_circ_310257,RMVar_hsa_circ_64111,RMVar_hsa_circ_75743,RMVar_hsa_circ_295306,RMVar_hsa_circ_302899,RMVar_hsa_circ_238090,RMVar_hsa_circ_303105,RMVar_hsa_circ_301794,RMVar_hsa_circ_126735,RMVar_hsa_circ_267006,RMVar_hsa_circ_124581,RMVar_hsa_circ_238093,RMVar_hsa_circ_238094,RMVar_hsa_circ_238095,RMVar_hsa_circ_238092 19650 RMVar_ID_19650 Human_SNP_ID_273073661 A-to-I Human chr6 - 35855045 35855045 35855045 CGCCCACTTCTGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCGCTGGGCCCATATCA CGCCCACTTCTGCCTCCCAAAGTGCTGGGATTGCAGGTGTGAGCCACCGCGCTGGGCCCATATCA T C SRPK1 Ensembl:ENSG00000096063 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1240147834 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123766,RMVar_hsa_circ_118747,RMVar_hsa_circ_238091,RMVar_hsa_circ_7460,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_109295,RMVar_hsa_circ_238089,RMVar_hsa_circ_310257,RMVar_hsa_circ_64111,RMVar_hsa_circ_75743,RMVar_hsa_circ_295306,RMVar_hsa_circ_302899,RMVar_hsa_circ_238090,RMVar_hsa_circ_303105,RMVar_hsa_circ_301794,RMVar_hsa_circ_126735,RMVar_hsa_circ_267006,RMVar_hsa_circ_124581,RMVar_hsa_circ_238093,RMVar_hsa_circ_238094,RMVar_hsa_circ_238095,RMVar_hsa_circ_238092 19651 RMVar_ID_19651 Human_SNP_ID_273080317 A-to-I Human chr6 - 35882385 35882385 35882385 TCGAGCCTGGGAGTTTGAGGCTGCAGTGAGCTATGATAGTGCCACTGTACTCCAGTGTGGGTGGC TCGAGCCTGGGAGTTTGAGGCTGCAGTGAGCTCTGATAGTGCCACTGTACTCCAGTGTGGGTGGC T G SRPK1 Ensembl:ENSG00000096063 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs750485396 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17576314,Human_RBP_ID_24160303,Human_RBP_ID_26002370 RMVar_hsa_circ_2511,RMVar_hsa_circ_123766,RMVar_hsa_circ_118747,RMVar_hsa_circ_238091,RMVar_hsa_circ_7460,RMVar_hsa_circ_103015,RMVar_hsa_circ_238087,RMVar_hsa_circ_238088,RMVar_hsa_circ_238086,RMVar_hsa_circ_301794,RMVar_hsa_circ_126735,RMVar_hsa_circ_124581,RMVar_hsa_circ_238092,RMVar_hsa_circ_7794,RMVar_hsa_circ_299734,RMVar_hsa_circ_371623,RMVar_hsa_circ_277387,RMVar_hsa_circ_96458,RMVar_hsa_circ_238099,RMVar_hsa_circ_238101,RMVar_hsa_circ_238102,RMVar_hsa_circ_238100,RMVar_hsa_circ_31654,RMVar_hsa_circ_329836,RMVar_hsa_circ_238105,RMVar_hsa_circ_11759,RMVar_hsa_circ_111504,RMVar_hsa_circ_296579,RMVar_hsa_circ_238107,RMVar_hsa_circ_238108,RMVar_hsa_circ_301346,RMVar_hsa_circ_319559,RMVar_hsa_circ_291853,RMVar_hsa_circ_238109,RMVar_hsa_circ_238110 19652 RMVar_ID_19652 Human_SNP_ID_273080534 A-to-I Human chr6 - 35883342 35883342 35883342 TCTTGTTGGCCAGGCTGGAGTGCAATGGCGCAATCTCGGCTCACTGCAACCTCCGCCTCCCAGGT TCTTGTTGGCCAGGCTGGAGTGCAATGGCGCAGTCTCGGCTCACTGCAACCTCCGCCTCCCAGGT T C SRPK1 Ensembl:ENSG00000096063 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs916015962 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2511,RMVar_hsa_circ_123766,RMVar_hsa_circ_118747,RMVar_hsa_circ_238091,RMVar_hsa_circ_7460,RMVar_hsa_circ_103015,RMVar_hsa_circ_238087,RMVar_hsa_circ_238088,RMVar_hsa_circ_238086,RMVar_hsa_circ_301794,RMVar_hsa_circ_126735,RMVar_hsa_circ_124581,RMVar_hsa_circ_238092,RMVar_hsa_circ_7794,RMVar_hsa_circ_299734,RMVar_hsa_circ_371623,RMVar_hsa_circ_277387,RMVar_hsa_circ_96458,RMVar_hsa_circ_238099,RMVar_hsa_circ_238101,RMVar_hsa_circ_238102,RMVar_hsa_circ_238100,RMVar_hsa_circ_31654,RMVar_hsa_circ_329836,RMVar_hsa_circ_238105,RMVar_hsa_circ_11759,RMVar_hsa_circ_111504,RMVar_hsa_circ_296579,RMVar_hsa_circ_238107,RMVar_hsa_circ_238108,RMVar_hsa_circ_301346,RMVar_hsa_circ_319559,RMVar_hsa_circ_291853,RMVar_hsa_circ_238109,RMVar_hsa_circ_238110 19653 RMVar_ID_19653 Human_SNP_ID_273082838 A-to-I Human chr6 - 35892589 35892589 35892589 GGAGTGCAACGACGCGATTTCGGCTCACTGTAACCTTTGCCTCCTGAGTTCAAGTGATTATTGTG GGAGTGCAACGACGCGATTTCGGCTCACTGTAGCCTTTGCCTCCTGAGTTCAAGTGATTATTGTG T C SRPK1 Ensembl:ENSG00000096063 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs942310054 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118747,RMVar_hsa_circ_238091,RMVar_hsa_circ_7460,RMVar_hsa_circ_238088,RMVar_hsa_circ_126735,RMVar_hsa_circ_299734 19654 RMVar_ID_19654 Human_SNP_ID_273082839 A-to-I Human chr6 - 35892590 35892590 35892590 TGGAGTGCAACGACGCGATTTCGGCTCACTGTAACCTTTGCCTCCTGAGTTCAAGTGATTATTGT TGGAGTGCAACGACGCGATTTCGGCTCACTGTGACCTTTGCCTCCTGAGTTCAAGTGATTATTGT T C SRPK1 Ensembl:ENSG00000096063 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432065132 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118747,RMVar_hsa_circ_238091,RMVar_hsa_circ_7460,RMVar_hsa_circ_238088,RMVar_hsa_circ_126735,RMVar_hsa_circ_299734 19655 RMVar_ID_19655 Human_SNP_ID_273088218 A-to-I Human chr6 - 35915076 35915076 35915076 ATTTAACAGGTTTGGCCGGGCACAGTGGCTCAAGCCTGTAATCCTGGCACTTTGGGAGGCTGAGG ATTTAACAGGTTTGGCCGGGCACAGTGGCTCATGCCTGTAATCCTGGCACTTTGGGAGGCTGAGG T A SRPK1 Ensembl:ENSG00000096063 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1035670298 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15808253 RMVar_hsa_circ_118747,RMVar_hsa_circ_238091,RMVar_hsa_circ_7460,RMVar_hsa_circ_238088,RMVar_hsa_circ_126735,RMVar_hsa_circ_299734 19656 RMVar_ID_19656 Human_SNP_ID_273098958 A-to-I Human chr6 - 35960084 35960084 35960084 GCCAACATGGTGAAACCCCGTATCTACTAAAAATACAAAAATTAGCAGGGCGTGATGGCAGGTGC GCCAACATGGTGAAACCCCGTATCTACTAAAAGTACAAAAATTAGCAGGGCGTGATGGCAGGTGC T C SLC26A8 Ensembl:ENSG00000112053 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1026154505 Functional Loss SNV dbSNP153 33..33 33 - - - 19657 RMVar_ID_19657 Human_SNP_ID_273120353 A-to-I Human chr6 + 36051369 36051369 36051369 CTGACCTCGTGATCCTCCCGCCTCGGCCTCCCAAGGTGCTGGATTACAGGCATGAGCCACTGTGC CTGACCTCGTGATCCTCCCGCCTCGGCCTCCCGAGGTGCTGGATTACAGGCATGAGCCACTGTGC A G MAPK14 Ensembl:ENSG00000112062 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1021873201 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21604,RMVar_hsa_circ_61855 19658 RMVar_ID_19658 Human_SNP_ID_273123101 A-to-I Human chr6 + 36064161 36064161 36064161 ACCACTAGACTCAGCTGTTTTTATTTTTTTGTAAAGACAAGGCCTTGCTATGTTGCCTTGGTTGG ACCACTAGACTCAGCTGTTTTTATTTTTTTGTGAAGACAAGGCCTTGCTATGTTGCCTTGGTTGG A G MAPK14 Ensembl:ENSG00000112062 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs574053962 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15808777 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 19659 RMVar_ID_19659 Human_SNP_ID_273131559 A-to-I Human chr6 + 36101626 36101625 36101626 GGGCTCCATCTCCCTGCTCAAGCGATCCTGTTACCTCAGTCTCCCAAGTAGCTGGGACCACAGGC GGGCTCCATCTCCCTGCTCAAGCGATCCTGTT_CCTCAGTCTCCCAAGTAGCTGGGACCACAGGC TA T MAPK14 Ensembl:ENSG00000112062 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1186536682 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_17576323 RMVar_hsa_circ_19317,RMVar_hsa_circ_266981,RMVar_hsa_circ_275682,RMVar_hsa_circ_30071,RMVar_hsa_circ_238118 19660 RMVar_ID_19660 Human_SNP_ID_273131565 A-to-I Human chr6 + 36101643 36101643 36101643 TCAAGCGATCCTGTTACCTCAGTCTCCCAAGTAGCTGGGACCACAGGCATGCGTCACCACACCTG TCAAGCGATCCTGTTACCTCAGTCTCCCAAGTTGCTGGGACCACAGGCATGCGTCACCACACCTG A T MAPK14 Ensembl:ENSG00000112062 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs930703192 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17576323 RMVar_hsa_circ_19317,RMVar_hsa_circ_266981,RMVar_hsa_circ_275682,RMVar_hsa_circ_30071,RMVar_hsa_circ_238118 19661 RMVar_ID_19661 Human_SNP_ID_273136962 A-to-I Human chr6 + 36125318 36125318 36125318 ACCAGCATTTTAAATTACTTGTTTATTGAGACAAGGTCTCGCTCTGTTGCCCAGGCTGAAGTGCA ACCAGCATTTTAAATTACTTGTTTATTGAGACTAGGTCTCGCTCTGTTGCCCAGGCTGAAGTGCA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1369290359 Functional Loss SNV dbSNP153 33..33 33 - - - 19662 RMVar_ID_19662 Human_SNP_ID_273136991 A-to-I Human chr6 + 36125470 36125470 36125470 GCTTGGCTAATTTTTATTATTATTGTTAGTAGAAACAGGGTTTCACCATGTTGTCCAGGCTGGTC GCTTGGCTAATTTTTATTATTATTGTTAGTAGGAACAGGGTTTCACCATGTTGTCCAGGCTGGTC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1356221834 Functional Loss SNV dbSNP153 33..33 33 - - - 19663 RMVar_ID_19663 Human_SNP_ID_273136996 A-to-I Human chr6 + 36125482 36125482 36125482 TTTATTATTATTGTTAGTAGAAACAGGGTTTCACCATGTTGTCCAGGCTGGTCTCAAACTCCTGG TTTATTATTATTGTTAGTAGAAACAGGGTTTCTCCATGTTGTCCAGGCTGGTCTCAAACTCCTGG A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1158944350 Functional Loss SNV dbSNP153 33..33 33 - - - 19664 RMVar_ID_19664 Human_SNP_ID_273137005 A-to-I Human chr6 + 36125537 36125537 36125537 AAACTCCTGGGTTCAAGTGATCCTCCCACCCCAGCCTCCCAAAGTGCTGGGATACAGCCATGAGC AAACTCCTGGGTTCAAGTGATCCTCCCACCCCGGCCTCCCAAAGTGCTGGGATACAGCCATGAGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049542992 Functional Loss SNV dbSNP153 33..33 33 - - - 19665 RMVar_ID_19665 Human_SNP_ID_273137816 A-to-I Human chr6 + 36129129 36129129 36129129 GGGCCAGGTGCGGTGGCTCACTTCTGTAATCCAAACACTTTGGGAGGCTGAGGTGGGCGGACCAC GGGCCAGGTGCGGTGGCTCACTTCTGTAATCCCAACACTTTGGGAGGCTGAGGTGGGCGGACCAC A C MAPK13 Ensembl:ENSG00000156711 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1346091872 Functional Loss SNV dbSNP153 33..33 33 - - - 19666 RMVar_ID_19666 Human_SNP_ID_273137989 A-to-I Human chr6 + 36129623 36129623 36129623 TAAAAATACAAAAATTAGCCGGGTTTGGTGGCAGGCACCTACAATCCTAGCTAATCGGGAGGCGG TAAAAATACAAAAATTAGCCGGGTTTGGTGGCGGGCACCTACAATCCTAGCTAATCGGGAGGCGG A G MAPK13 Ensembl:ENSG00000156711 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1003136795 Functional Loss SNV dbSNP153 33..33 33 - - - 19667 RMVar_ID_19667 Human_SNP_ID_273141385 A-to-I Human chr6 + 36141472 36141465 36141473 GAGGTGGGCGGATCACTTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCCCAT GAGGTGGGCGGATCACTTGAGGTCAG________GACCAGCCTGGCCAACATGGTGAAACCCCAT GGAGTTCAA G MAPK13 Ensembl:ENSG00000156711 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1561792608 Functional Loss DEL dbSNP153 27..34 33 - - - Human_RBP_ID_172235 19668 RMVar_ID_19668 Human_SNP_ID_273141410 A-to-I Human chr6 + 36141592 36141592 36141592 AACTACTCGGGAGGCTGAGGCAGAATTGCTTGAACCTGGGAGGTGGAGGTTGCAGTGAGCTGAGA AACTACTCGGGAGGCTGAGGCAGAATTGCTTGGACCTGGGAGGTGGAGGTTGCAGTGAGCTGAGA A G MAPK13 Ensembl:ENSG00000156711 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 31158229,32596459 RNA-Seq:(High) rs1035630511 Functional Loss SNV dbSNP153 33..33 33 - - - 19669 RMVar_ID_19669 Human_SNP_ID_273217843 A-to-I Human chr6 + 36454737 36454737 36454737 CTCAGCTCACTGCAACCTCCGCCGCCGGGTTCAAGCAGTTCTCCCGCCTCAGTCTCCCAAGTACC CTCAGCTCACTGCAACCTCCGCCGCCGGGTTCCAGCAGTTCTCCCGCCTCAGTCTCCCAAGTACC A C KCTD20 Ensembl:ENSG00000112078 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1408930831 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_238130 19670 RMVar_ID_19670 Human_SNP_ID_273218321 A-to-I Human chr6 + 36456705 36456705 36456705 GACCTCCTGAGCTCAAATGACCTTCCTGCCTCAGCCTCCTGAGTAGCTGAGACTACAAGTGTGCA GACCTCCTGAGCTCAAATGACCTTCCTGCCTCTGCCTCCTGAGTAGCTGAGACTACAAGTGTGCA A T KCTD20 Ensembl:ENSG00000112078 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1222537906 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_238130 19671 RMVar_ID_19671 Human_SNP_ID_273218377 A-to-I Human chr6 + 36456939 36456939 36456939 CAAACCTTGGCCTCTCAAGTAGCTGGGACTACAGGCATATGCCACCATGCCTGGCTAATTTTTTT CAAACCTTGGCCTCTCAAGTAGCTGGGACTACGGGCATATGCCACCATGCCTGGCTAATTTTTTT A G KCTD20 Ensembl:ENSG00000112078 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1454251221 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_238130 19672 RMVar_ID_19672 Human_SNP_ID_273218490 A-to-I Human chr6 + 36457450 36457450 36457450 AATGTTGAGGCCGGGTACGGGGACTCACGCCTATAATTCCAATGCTTTGGGAGGCCCAGGTGGGA AATGTTGAGGCCGGGTACGGGGACTCACGCCTGTAATTCCAATGCTTTGGGAGGCCCAGGTGGGA A G KCTD20 Ensembl:ENSG00000112078 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs76019396 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22482641 GWAS_ID_1726,GWAS_ID_1727,GWAS_ID_1728,GWAS_ID_1729,GWAS_ID_1730,GWAS_ID_1731,GWAS_ID_1732,GWAS_ID_1733,GWAS_ID_1734,GWAS_ID_1735,GWAS_ID_1736,GWAS_ID_1737,GWAS_ID_1738 RMVar_hsa_circ_238130 19673 RMVar_ID_19673 Human_SNP_ID_273218517 A-to-I Human chr6 + 36457593 36457593 36457593 AAAATTAGCTGGGCATGGTTGTGCATACCTGTAATACCAGCTACTTGGGAGGCTGAGGCAGGAGG AAAATTAGCTGGGCATGGTTGTGCATACCTGTCATACCAGCTACTTGGGAGGCTGAGGCAGGAGG A C KCTD20 Ensembl:ENSG00000112078 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1561945917 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_238130 19674 RMVar_ID_19674 Human_SNP_ID_273220644 A-to-I Human chr6 + 36467478 36467478 36467478 CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCCCCACCACGCCCGGGTAATTTTTG CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTGCAGGCGCCCCCACCACGCCCGGGTAATTTTTG A G KCTD20 Ensembl:ENSG00000112078 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1191796062 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_309859 19675 RMVar_ID_19675 Human_SNP_ID_273221289 A-to-I Human chr6 + 36470740 36470740 36470740 CTCTCACCTCAGCCTCACGAGTTGCTGGGACCACAGGTGGGTACCACCACACCCAGCTAACTTTT CTCTCACCTCAGCCTCACGAGTTGCTGGGACCGCAGGTGGGTACCACCACACCCAGCTAACTTTT A G KCTD20 Ensembl:ENSG00000112078 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs193035154 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_312585,RMVar_hsa_circ_334347,RMVar_hsa_circ_294747,RMVar_hsa_circ_238131 19676 RMVar_ID_19676 Human_SNP_ID_273221918 A-to-I Human chr6 + 36473296 36473295 36473297 GTTAGCCAGGATGGTCTCGATCTCCTGACCTCAGATGATCTGCCCACCTTGGCTTCCCAAAGTGC GTTAGCCAGGATGGTCTCGATCTCCTGACCTC__ATGATCTGCCCACCTTGGCTTCCCAAAGTGC CAG C KCTD20 Ensembl:ENSG00000112078 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1280598380 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_312585,RMVar_hsa_circ_334347,RMVar_hsa_circ_294747,RMVar_hsa_circ_238131 19677 RMVar_ID_19677 Human_SNP_ID_273224287 A-to-I Human chr6 + 36482784 36482783 36482784 CCTTGCCAATATAGTGAAACCCCATCTCTATTAAAAATACAAAAATTAGCTGGGCGTCGTGGCTC CCTTGCCAATATAGTGAAACCCCATCTCTATT_AAAATACAAAAATTAGCTGGGCGTCGTGGCTC TA T KCTD20 Ensembl:ENSG00000112078 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1298250059 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_312585,RMVar_hsa_circ_361148,RMVar_hsa_circ_336507 19678 RMVar_ID_19678 Human_SNP_ID_273224539 A-to-I Human chr6 + 36483393 36483393 36483393 TGCCACCACGTCCGGCTAATTTTTGTATTATTAATAGAAACGGGGTTTCACCATGTTGGCCAGGC TGCCACCACGTCCGGCTAATTTTTGTATTATTGATAGAAACGGGGTTTCACCATGTTGGCCAGGC A G KCTD20 Ensembl:ENSG00000112078 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs914601214 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_312585,RMVar_hsa_circ_361148,RMVar_hsa_circ_336507 19679 RMVar_ID_19679 Human_SNP_ID_273224578 A-to-I Human chr6 + 36483558 36483558 36483558 TTTTTTACAGATAGAATCTTGCTCTTTCACCCAGGCTGGAGAGCAGTGGTGCAATCATGGCTCAC TTTTTTACAGATAGAATCTTGCTCTTTCACCCCGGCTGGAGAGCAGTGGTGCAATCATGGCTCAC A C KCTD20 Ensembl:ENSG00000112078 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1219740115 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_312585,RMVar_hsa_circ_361148,RMVar_hsa_circ_336507 19680 RMVar_ID_19680 Human_SNP_ID_273224724 A-to-I Human chr6 + 36484136 36484136 36484136 TTTTCTATTTTTAGTAGAGACGGGGTTTCACCATGTTAGTCAGGCTGGTCTCCAACTCCCAACCT TTTTCTATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGTCAGGCTGGTCTCCAACTCCCAACCT A G KCTD20 Ensembl:ENSG00000112078 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs900233380 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_312585,RMVar_hsa_circ_361148,RMVar_hsa_circ_336507 19681 RMVar_ID_19681 Human_SNP_ID_273226242 A-to-I Human chr6 + 36490390 36490390 36490390 AACCCCGTCTCTACTAAAAATACAAAAAAATTAGCCCGGTGTGGTGGCAAGTGCCTGTAGTCCCA AACCCCGTCTCTACTAAAAATACAAAAAAATTGGCCCGGTGTGGTGGCAAGTGCCTGTAGTCCCA A G KCTD20 Ensembl:ENSG00000112078 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs936857336 Functional Loss SNV dbSNP153 33..33 33 - - - 19682 RMVar_ID_19682 Human_SNP_ID_273230510 A-to-I Human chr6 - 36508054 36508054 36508054 TGGCACACAACTGAGGTCCCAGCTACTCAGGAAGCTGAGTTGGGAGGATTGCTTGAACCTGGGAG TGGCACACAACTGAGGTCCCAGCTACTCAGGAGGCTGAGTTGGGAGGATTGCTTGAACCTGGGAG T C STK38 Ensembl:ENSG00000112079 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1172773729 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_345671,RMVar_hsa_circ_361386,RMVar_hsa_circ_362649,RMVar_hsa_circ_353305,RMVar_hsa_circ_284228,RMVar_hsa_circ_73404,RMVar_hsa_circ_8592,RMVar_hsa_circ_47842,RMVar_hsa_circ_238138,RMVar_hsa_circ_238136,RMVar_hsa_circ_48576,RMVar_hsa_circ_368683,RMVar_hsa_circ_292055,RMVar_hsa_circ_47656,RMVar_hsa_circ_350126,RMVar_hsa_circ_360054,RMVar_hsa_circ_338264,RMVar_hsa_circ_105138,RMVar_hsa_circ_238140 19683 RMVar_ID_19683 Human_SNP_ID_273230542 A-to-I Human chr6 - 36508211 36508211 36508211 GTAATTTTGGCCAGGTGTGGTGGCGCATGCCTATAATCTCAGAACTTTGGGAGGCTGGGATGGGA GTAATTTTGGCCAGGTGTGGTGGCGCATGCCTGTAATCTCAGAACTTTGGGAGGCTGGGATGGGA T C STK38 Ensembl:ENSG00000112079 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1257447831 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26047203 RMVar_hsa_circ_345671,RMVar_hsa_circ_361386,RMVar_hsa_circ_362649,RMVar_hsa_circ_353305,RMVar_hsa_circ_284228,RMVar_hsa_circ_73404,RMVar_hsa_circ_8592,RMVar_hsa_circ_47842,RMVar_hsa_circ_238138,RMVar_hsa_circ_238136,RMVar_hsa_circ_48576,RMVar_hsa_circ_368683,RMVar_hsa_circ_292055,RMVar_hsa_circ_47656,RMVar_hsa_circ_350126,RMVar_hsa_circ_360054,RMVar_hsa_circ_338264,RMVar_hsa_circ_105138,RMVar_hsa_circ_238140 19684 RMVar_ID_19684 Human_SNP_ID_273231404 A-to-I Human chr6 - 36511494 36511494 36511494 AAAATTAGCCAGATGTGGTGGCGGGCACCTGTAATCCCAGCTACTCAGGTGGCTGAGGCAGAGAA AAAATTAGCCAGATGTGGTGGCGGGCACCTGTTATCCCAGCTACTCAGGTGGCTGAGGCAGAGAA T A STK38 Ensembl:ENSG00000112079 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs976847431 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_345671,RMVar_hsa_circ_361386,RMVar_hsa_circ_362649,RMVar_hsa_circ_353305,RMVar_hsa_circ_284228,RMVar_hsa_circ_73404,RMVar_hsa_circ_8592,RMVar_hsa_circ_47842,RMVar_hsa_circ_238138,RMVar_hsa_circ_238136,RMVar_hsa_circ_48576,RMVar_hsa_circ_368683,RMVar_hsa_circ_292055,RMVar_hsa_circ_47656,RMVar_hsa_circ_350126,RMVar_hsa_circ_360054,RMVar_hsa_circ_338264,RMVar_hsa_circ_105138,RMVar_hsa_circ_238140 19685 RMVar_ID_19685 Human_SNP_ID_273231522 A-to-I Human chr6 - 36511983 36511983 36511983 GTGATCTTGGCTCACTGTGACTTCTGCCTCCCAGTTTCAAGCAATTCTCCTGCCTCAGCCTCCCA GTGATCTTGGCTCACTGTGACTTCTGCCTCCCCGTTTCAAGCAATTCTCCTGCCTCAGCCTCCCA T G STK38 Ensembl:ENSG00000112079 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1309807088 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_345671,RMVar_hsa_circ_361386,RMVar_hsa_circ_362649,RMVar_hsa_circ_353305,RMVar_hsa_circ_284228,RMVar_hsa_circ_73404,RMVar_hsa_circ_8592,RMVar_hsa_circ_47842,RMVar_hsa_circ_238138,RMVar_hsa_circ_238136,RMVar_hsa_circ_48576,RMVar_hsa_circ_368683,RMVar_hsa_circ_292055,RMVar_hsa_circ_47656,RMVar_hsa_circ_350126,RMVar_hsa_circ_360054,RMVar_hsa_circ_338264,RMVar_hsa_circ_105138,RMVar_hsa_circ_238140 19686 RMVar_ID_19686 Human_SNP_ID_273232205 A-to-I Human chr6 - 36514234 36514234 36514234 TTATAGCTCACTGCAATCTAATTCTTGGGTTCAAGGGATCCTCTTGCCTCAGCCTCCTGAGTAGT TTATAGCTCACTGCAATCTAATTCTTGGGTTCTAGGGATCCTCTTGCCTCAGCCTCCTGAGTAGT T A STK38 Ensembl:ENSG00000112079 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1485837253 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_345671,RMVar_hsa_circ_361386,RMVar_hsa_circ_362649,RMVar_hsa_circ_353305,RMVar_hsa_circ_284228,RMVar_hsa_circ_73404,RMVar_hsa_circ_8592,RMVar_hsa_circ_47842,RMVar_hsa_circ_238138,RMVar_hsa_circ_238136,RMVar_hsa_circ_48576,RMVar_hsa_circ_368683,RMVar_hsa_circ_292055,RMVar_hsa_circ_47656,RMVar_hsa_circ_350126,RMVar_hsa_circ_360054,RMVar_hsa_circ_338264,RMVar_hsa_circ_105138,RMVar_hsa_circ_238140 19687 RMVar_ID_19687 Human_SNP_ID_273239361 A-to-I Human chr6 - 36541957 36541957 36541957 GGGCACAGTGGCTGGTGCCTGTCATCTTAACTACTTGGGAGGCTGAGACACGAGAATCGCTTGAA GGGCACAGTGGCTGGTGCCTGTCATCTTAACTGCTTGGGAGGCTGAGACACGAGAATCGCTTGAA T C STK38 Ensembl:ENSG00000112079 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1457222256 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15811567 19688 RMVar_ID_19688 Human_SNP_ID_273239400 A-to-I Human chr6 - 36542107 36542107 36542107 ACATGGGCTGGGTGCAGTGGCTCATGCCTGCAATCCCAGCACTTTGGGAGGCCAAGTTGGGTGGA ACATGGGCTGGGTGCAGTGGCTCATGCCTGCAGTCCCAGCACTTTGGGAGGCCAAGTTGGGTGGA T C STK38 Ensembl:ENSG00000112079 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs949742924 Functional Loss SNV dbSNP153 33..33 33 - - - 19689 RMVar_ID_19689 Human_SNP_ID_273239581 A-to-I Human chr6 - 36542749 36542749 36542749 TAGAGACGGGGTTTCACTCTGTTGGTCAGGCTAGTCTCCCAACTCCTGACCTCAGATGATTCGCC TAGAGACGGGGTTTCACTCTGTTGGTCAGGCTGGTCTCCCAACTCCTGACCTCAGATGATTCGCC T C STK38 Ensembl:ENSG00000112079 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs986671032 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7600727 19690 RMVar_ID_19690 Human_SNP_ID_273239791 A-to-I Human chr6 - 36543515 36543515 36543515 CTCATGAACTCCTGGGCTCAAATGATCTCTCTACCTCACCCTCCCAAAGTGATGGGATTACAGGC CTCATGAACTCCTGGGCTCAAATGATCTCTCTGCCTCACCCTCCCAAAGTGATGGGATTACAGGC T C STK38 Ensembl:ENSG00000112079 Protein coding intron GSE100210;GSE99789 HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 29129909,29796672 RNA-Seq:(High) rs1212508184 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17576324 19691 RMVar_ID_19691 Human_SNP_ID_273239792 A-to-I Human chr6 - 36543527 36543527 36543527 TGAATTCCTGGACTCATGAACTCCTGGGCTCAAATGATCTCTCTACCTCACCCTCCCAAAGTGAT TGAATTCCTGGACTCATGAACTCCTGGGCTCAGATGATCTCTCTACCTCACCCTCCCAAAGTGAT T C STK38 Ensembl:ENSG00000112079 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs896938437 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17576324 19692 RMVar_ID_19692 Human_SNP_ID_273239807 A-to-I Human chr6 - 36543578 36543578 36543578 GCTGTGGGGGGTAGTAGAGACAGGGTCTTGCTATGTTACCCAGGCTGGTCTTGAATTCCTGGACT GCTGTGGGGGGTAGTAGAGACAGGGTCTTGCTGTGTTACCCAGGCTGGTCTTGAATTCCTGGACT T C STK38 Ensembl:ENSG00000112079 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs528778462 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17576324 19693 RMVar_ID_19693 Human_SNP_ID_273240094 A-to-I Human chr6 - 36544700 36544700 36544700 ACCTGGCCAATTTTTTGTATTTTTTTGTAGCAACGGGGGTTTTGCCATGTTGCACAGGCTGGTTT ACCTGGCCAATTTTTTGTATTTTTTTGTAGCAGCGGGGGTTTTGCCATGTTGCACAGGCTGGTTT T C STK38 Ensembl:ENSG00000112079 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs866489797 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15811631 19694 RMVar_ID_19694 Human_SNP_ID_273240111 A-to-I Human chr6 - 36544785 36544785 36544785 TCACTGAAACCTCTGCCTCTCCAGCTCAAGCAATCCTCCCACCTCAGCCTCCTGAGTAGCTGGGA TCACTGAAACCTCTGCCTCTCCAGCTCAAGCAGTCCTCCCACCTCAGCCTCCTGAGTAGCTGGGA T C STK38 Ensembl:ENSG00000112079 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs191104071 Functional Loss SNV dbSNP153 33..33 33 - - - 19695 RMVar_ID_19695 Human_SNP_ID_273240113 A-to-I Human chr6 - 36544789 36544789 36544789 AAACTCACTGAAACCTCTGCCTCTCCAGCTCAAGCAATCCTCCCACCTCAGCCTCCTGAGTAGCT AAACTCACTGAAACCTCTGCCTCTCCAGCTCACGCAATCCTCCCACCTCAGCCTCCTGAGTAGCT T G STK38 Ensembl:ENSG00000112079 Protein coding intron GSE100210;GSE99789 HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 29129909,29796672 RNA-Seq:(High) rs1487135420 Functional Loss SNV dbSNP153 33..33 33 - - - 19696 RMVar_ID_19696 Human_SNP_ID_273252580 A-to-I Human chr6 - 36592247 36592247 36592247 GCAATTCTCCTACCTCAGCCTCCCCAACGACTAGGACCACAGGCGCGAGCACAGATGCCCAGCTA GCAATTCTCCTACCTCAGCCTCCCCAACGACTGGGACCACAGGCGCGAGCACAGATGCCCAGCTA T C RF00017-4575,RF00017-4630 RNACentral:URS0000918622,RNACentral:URS000096585E SRP RNA,SRP RNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs374622310 Functional Loss SNV dbSNP153 33..33 33 - - - 19697 RMVar_ID_19697 Human_SNP_ID_273257417 A-to-I Human chr6 + 36606554 36606554 36606554 TAATGTTATTTATGTATTTTTTTTTTTTTTTGAGATGGAGTCTCTCTTTGTCACCCAGGCTGGAG TAATGTTATTTATGTATTTTTTTTTTTTTTTGTGATGGAGTCTCTCTTTGTCACCCAGGCTGGAG A T RF00017-5484 RNACentral:URS00009A6CA9 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1262302996 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7601087,Human_RBP_ID_15812427 19698 RMVar_ID_19698 Human_SNP_ID_273266116 A-to-I Human chr6 + 36640069 36640069 36640069 CCTTGGCCTCCCAAAGTGCTAGGATTACAGGCATGAACCACCAGGCCCGGCCCTCCTCATTTTTT CCTTGGCCTCCCAAAGTGCTAGGATTACAGGCCTGAACCACCAGGCCCGGCCCTCCTCATTTTTT A C RF00017-5484 RNACentral:URS00009A6CA9 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1263035273 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15813617 19699 RMVar_ID_19699 Human_SNP_ID_273273950 A-to-I Human chr6 + 36674104 36674104 36674104 GGCAAAGAAAACATCAGAGCTGCTGTTGCAGCAGGATGCAGGCAGATTCAAGACCTGGAGCTCTC GGCAAAGAAAACATCAGAGCTGCTGTTGCAGCGGGATGCAGGCAGATTCAAGACCTGGAGCTCTC A G LAP3P2 Ensembl:ENSG00000213500 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878979331 Functional Loss SNV dbSNP153 33..33 33 - - - 19700 RMVar_ID_19700 Human_SNP_ID_273273952 A-to-I Human chr6 + 36674107 36674107 36674107 AAAGAAAACATCAGAGCTGCTGTTGCAGCAGGATGCAGGCAGATTCAAGACCTGGAGCTCTCTTC AAAGAAAACATCAGAGCTGCTGTTGCAGCAGGGTGCAGGCAGATTCAAGACCTGGAGCTCTCTTC A G LAP3P2 Ensembl:ENSG00000213500 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878952682 Functional Loss SNV dbSNP153 33..33 33 - - - 19701 RMVar_ID_19701 Human_SNP_ID_273274157 A-to-I Human chr6 + 36674879 36674879 36674879 ACACATTTAACCCGAAGGTCATCCTCAATGCCACCACCTTAACAGGTGTCATAGATGTAGCTTTG ACACATTTAACCCGAAGGTCATCCTCAATGCCGCCACCTTAACAGGTGTCATAGATGTAGCTTTG A G LAP3P2 Ensembl:ENSG00000213500 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879230448 Functional Loss SNV dbSNP153 33..33 33 - - - 19702 RMVar_ID_19702 Human_SNP_ID_273274162 A-to-I Human chr6 + 36674899 36674899 36674899 ATCCTCAATGCCACCACCTTAACAGGTGTCATAGATGTAGCTTTGGGGTCAGGTGCCACTGGGGT ATCCTCAATGCCACCACCTTAACAGGTGTCATGGATGTAGCTTTGGGGTCAGGTGCCACTGGGGT A G LAP3P2 Ensembl:ENSG00000213500 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1242500366 Functional Loss SNV dbSNP153 33..33 33 - - - 19703 RMVar_ID_19703 Human_SNP_ID_273320083 A-to-I Human chr6 - 36860328 36860328 36860328 CCACCTGAGTAGCTGTAGCTGGGACTGCAGGCACGCACAACCACGCCTGGCTAATTTTTGTAGAG CCACCTGAGTAGCTGTAGCTGGGACTGCAGGCGCGCACAACCACGCCTGGCTAATTTTTGTAGAG T C PPIL1 Ensembl:ENSG00000137168 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1402441754 Functional Loss SNV dbSNP153 33..33 33 - - - 19704 RMVar_ID_19704 Human_SNP_ID_273335214 A-to-I Human chr6 + 36924004 36924004 36924004 TCAGATAACTTTGAATTGCATTCAAGAAGTACACTTCTTTCCCATTGTCCGTGGCTCTTGGAGTC TCAGATAACTTTGAATTGCATTCAAGAAGTACGCTTCTTTCCCATTGTCCGTGGCTCTTGGAGTC A G C6orf89 Ensembl:ENSG00000198663 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs141513302 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_663791,Human_RBP_ID_3808403,Human_RBP_ID_17307037,Human_RBP_ID_18865023,Human_RBP_ID_24161066,Human_RBP_ID_26536376 RMVar_hsa_circ_238163,RMVar_hsa_circ_123465 19705 RMVar_ID_19705 Human_SNP_ID_273335605 A-to-I Human chr6 + 36925926 36925926 36925926 AACCAACTCCCCACCTCCACCACCACAATAAGAACAAAACTGTAGGGCTCTAAAGAGAGGGGGTG AACCAACTCCCCACCTCCACCACCACAATAAGGACAAAACTGTAGGGCTCTAAAGAGAGGGGGTG A G C6orf89 Ensembl:ENSG00000198663 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs3179985 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_238163,RMVar_hsa_circ_123465 19706 RMVar_ID_19706 Human_SNP_ID_273342839 A-to-I Human chr6 + 36953163 36953162 36953163 ACATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTTGCCGGGCATGGTAGCAGCTATGGTG ACATGGTGAAACCCCATCTCTACTAAAAATAC_AAAATTTGCCGGGCATGGTAGCAGCTATGGTG CA C PI16 Ensembl:ENSG00000164530 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1561892901 Functional Loss DEL dbSNP153 33..33 33 - - - 19707 RMVar_ID_19707 Human_SNP_ID_273342868 A-to-I Human chr6 + 36953291 36953291 36953291 CCAGGAGGCAGAGGTTGCAGTGAGCCAAGATCATGCCACTGCACTCCAGCCTGGGTGACAGAGCG CCAGGAGGCAGAGGTTGCAGTGAGCCAAGATCCTGCCACTGCACTCCAGCCTGGGTGACAGAGCG A C PI16 Ensembl:ENSG00000164530 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs898795152 Functional Loss SNV dbSNP153 33..33 33 - - - 19708 RMVar_ID_19708 Human_SNP_ID_273348150 A-to-I Human chr6 - 36973900 36973900 36973900 TTAGAGGTGAAGTAAGTTGGATGTGAGGTGACAAAGTGCAGGGCATCTGTGGCCCTCAGGGACCA TTAGAGGTGAAGTAAGTTGGATGTGAGGTGACGAAGTGCAGGGCATCTGTGGCCCTCAGGGACCA T C MTCH1 Ensembl:ENSG00000137409 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1041319838 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23450,RMVar_hsa_circ_93491,RMVar_hsa_circ_96428,RMVar_hsa_circ_238167,RMVar_hsa_circ_88687,RMVar_hsa_circ_90665,RMVar_hsa_circ_87795,RMVar_hsa_circ_238168,RMVar_hsa_circ_238165,RMVar_hsa_circ_238166,RMVar_hsa_circ_238164,RMVar_hsa_circ_371207,RMVar_hsa_circ_238172 19709 RMVar_ID_19709 Human_SNP_ID_273348179 A-to-I Human chr6 - 36974024 36974024 36974024 CAGCATGTATGTCACCGCCTAGACCTTAAAACAGCAAGTCAAAAAACAACTCATCAAGCCTGGCT CAGCATGTATGTCACCGCCTAGACCTTAAAACGGCAAGTCAAAAAACAACTCATCAAGCCTGGCT T C MTCH1 Ensembl:ENSG00000137409 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs113236194 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23314977 RMVar_hsa_circ_23450,RMVar_hsa_circ_93491,RMVar_hsa_circ_96428,RMVar_hsa_circ_238167,RMVar_hsa_circ_88687,RMVar_hsa_circ_90665,RMVar_hsa_circ_87795,RMVar_hsa_circ_238168,RMVar_hsa_circ_238165,RMVar_hsa_circ_238166,RMVar_hsa_circ_238164,RMVar_hsa_circ_371207,RMVar_hsa_circ_238172 19710 RMVar_ID_19710 Human_SNP_ID_273348186 A-to-I Human chr6 - 36974055 36974055 36974055 GGTAACAAACCAACATTTGTGACATACCTATCAGCATGTATGTCACCGCCTAGACCTTAAAACAG GGTAACAAACCAACATTTGTGACATACCTATCGGCATGTATGTCACCGCCTAGACCTTAAAACAG T C MTCH1 Ensembl:ENSG00000137409 Protein coding intron GSE38233;GSE107867 cultured B-cells;ASD brains,cerebellum - 24183664,30559470 RNA-Seq:(High) rs572892018 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23450,RMVar_hsa_circ_93491,RMVar_hsa_circ_96428,RMVar_hsa_circ_238167,RMVar_hsa_circ_88687,RMVar_hsa_circ_90665,RMVar_hsa_circ_87795,RMVar_hsa_circ_238168,RMVar_hsa_circ_238165,RMVar_hsa_circ_238166,RMVar_hsa_circ_238164,RMVar_hsa_circ_371207,RMVar_hsa_circ_238172 19711 RMVar_ID_19711 Human_SNP_ID_273348423 A-to-I Human chr6 - 36974987 36974987 36974987 CACCTCTAAAGAAAGCACATACTGAAAAGACTAAGTTCAGAAAGAATAAGGTGCAGACAGAAGCC CACCTCTAAAGAAAGCACATACTGAAAAGACTGAGTTCAGAAAGAATAAGGTGCAGACAGAAGCC T C MTCH1 Ensembl:ENSG00000137409 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350965412 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23450,RMVar_hsa_circ_93491,RMVar_hsa_circ_96428,RMVar_hsa_circ_238167,RMVar_hsa_circ_88687,RMVar_hsa_circ_90665,RMVar_hsa_circ_87795,RMVar_hsa_circ_238168,RMVar_hsa_circ_238165,RMVar_hsa_circ_238166,RMVar_hsa_circ_238164,RMVar_hsa_circ_371207,RMVar_hsa_circ_238172 19712 RMVar_ID_19712 Human_SNP_ID_273348425 A-to-I Human chr6 - 36974999 36974999 36974999 TCCAGTGTACTTCACCTCTAAAGAAAGCACATACTGAAAAGACTAAGTTCAGAAAGAATAAGGTG TCCAGTGTACTTCACCTCTAAAGAAAGCACATGCTGAAAAGACTAAGTTCAGAAAGAATAAGGTG T C MTCH1 Ensembl:ENSG00000137409 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1016948703 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23450,RMVar_hsa_circ_93491,RMVar_hsa_circ_96428,RMVar_hsa_circ_238167,RMVar_hsa_circ_88687,RMVar_hsa_circ_90665,RMVar_hsa_circ_87795,RMVar_hsa_circ_238168,RMVar_hsa_circ_238165,RMVar_hsa_circ_238166,RMVar_hsa_circ_238164,RMVar_hsa_circ_371207,RMVar_hsa_circ_238172 19713 RMVar_ID_19713 Human_SNP_ID_273384612 A-to-I Human chr6 - 37115334 37115334 37115334 CAGGCTGGAGTGCAATGACGTGATCATAGCTCACTGCAGCCTCGACCTCCTGGGCTCCTTCCTGT CAGGCTGGAGTGCAATGACGTGATCATAGCTCGCTGCAGCCTCGACCTCCTGGGCTCCTTCCTGT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs967557907 Functional Loss SNV dbSNP153 33..33 33 - - - 19714 RMVar_ID_19714 Human_SNP_ID_273430488 A-to-I Human chr6 + 37299853 37299853 37299853 TCAACATGGCAAAACCCGTCTCTACCAAAAATACACAAATTAGCCGGGCATGGTGGCGGCTGCCT TCAACATGGCAAAACCCGTCTCTACCAAAAATGCACAAATTAGCCGGGCATGGTGGCGGCTGCCT A G TBC1D22B Ensembl:ENSG00000065491 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1001944868 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_368540,RMVar_hsa_circ_5998,RMVar_hsa_circ_119493,RMVar_hsa_circ_348545,RMVar_hsa_circ_238185,RMVar_hsa_circ_97563,RMVar_hsa_circ_238186,RMVar_hsa_circ_238184 19715 RMVar_ID_19715 Human_SNP_ID_273448552 A-to-I Human chr6 + 37378233 37378233 37378233 GGAGAATCACTTCAATTTGGGAGGCGGAGGCTACAGTGAGTCGAGATCACGCAACTGCACTTCAG GGAGAATCACTTCAATTTGGGAGGCGGAGGCTGCAGTGAGTCGAGATCACGCAACTGCACTTCAG A G RNF8 Ensembl:ENSG00000112130 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1217555984 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_30464,RMVar_hsa_circ_54833,RMVar_hsa_circ_309117,RMVar_hsa_circ_238197 19716 RMVar_ID_19716 Human_SNP_ID_273449199 A-to-I Human chr6 + 37380866 37380866 37380866 CACTGTGACTGGCTAATATTCGTATTTTTAGTAGAGACGAGGTTTTACCATGTTGCCCAGGCTGG CACTGTGACTGGCTAATATTCGTATTTTTAGTGGAGACGAGGTTTTACCATGTTGCCCAGGCTGG A G RNF8 Ensembl:ENSG00000112130 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1214996870 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_30464,RMVar_hsa_circ_54833,RMVar_hsa_circ_309117,RMVar_hsa_circ_238197 19717 RMVar_ID_19717 Human_SNP_ID_273449205 A-to-I Human chr6 + 37380883 37380883 37380883 ATTCGTATTTTTAGTAGAGACGAGGTTTTACCATGTTGCCCAGGCTGGTCTCAAACTCCTGACCT ATTCGTATTTTTAGTAGAGACGAGGTTTTACCGTGTTGCCCAGGCTGGTCTCAAACTCCTGACCT A G RNF8 Ensembl:ENSG00000112130 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1382371081 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_30464,RMVar_hsa_circ_54833,RMVar_hsa_circ_309117,RMVar_hsa_circ_238197 19718 RMVar_ID_19718 Human_SNP_ID_273450019 A-to-I Human chr6 + 37384274 37384274 37384274 GTGATTCTCCTCCCTCAGCCTCCTGGGTAGCTAGGATTACAGGTGCATGCCACCACGCCCAGCTC GTGATTCTCCTCCCTCAGCCTCCTGGGTAGCTGGGATTACAGGTGCATGCCACCACGCCCAGCTC A G RNF8 Ensembl:ENSG00000112130 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs748065029 Functional Loss SNV dbSNP153 33..33 33 - - - 19719 RMVar_ID_19719 Human_SNP_ID_273450256 A-to-I Human chr6 + 37385372 37385372 37385372 TATGCAGGGCGGGTGCTGTGGCTCACGGCTGTAATCCCAGCACTTTGGGAGGCTGAGGGGGCGTG TATGCAGGGCGGGTGCTGTGGCTCACGGCTGTGATCCCAGCACTTTGGGAGGCTGAGGGGGCGTG A G RNF8 Ensembl:ENSG00000112130 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1023983715 Functional Loss SNV dbSNP153 33..33 33 - - - 19720 RMVar_ID_19720 Human_SNP_ID_273465052 A-to-I Human chr6 + 37447690 37447690 37447690 CAAGACCAGCCTGACCAACATGACGAAACCCCATCTCTGCTAAAAATACAAAAACTAGCCAGGTG CAAGACCAGCCTGACCAACATGACGAAACCCCTTCTCTGCTAAAAATACAAAAACTAGCCAGGTG A T CMTR1 Ensembl:ENSG00000137200 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1214889061 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109730,RMVar_hsa_circ_853,RMVar_hsa_circ_238199,RMVar_hsa_circ_48730,RMVar_hsa_circ_31058,RMVar_hsa_circ_266856,RMVar_hsa_circ_26975 19721 RMVar_ID_19721 Human_SNP_ID_273465069 A-to-I Human chr6 + 37447752 37447752 37447752 GTGTGGGACTCACACCTGTAATTCCAGCTGCTAGAGAGGCTAAGGCAGGAGAATCACTTGAACCT GTGTGGGACTCACACCTGTAATTCCAGCTGCTGGAGAGGCTAAGGCAGGAGAATCACTTGAACCT A G CMTR1 Ensembl:ENSG00000137200 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs572347604 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109730,RMVar_hsa_circ_853,RMVar_hsa_circ_238199,RMVar_hsa_circ_48730,RMVar_hsa_circ_31058,RMVar_hsa_circ_266856,RMVar_hsa_circ_26975 19722 RMVar_ID_19722 Human_SNP_ID_273465369 A-to-I Human chr6 + 37449080 37449080 37449080 CTCTCACCTCAGCCTTCTGAGTATCTACAACTACAGGCCTGTGCCACCATGCCTGGCTAATTTTT CTCTCACCTCAGCCTTCTGAGTATCTACAACTGCAGGCCTGTGCCACCATGCCTGGCTAATTTTT A G CMTR1 Ensembl:ENSG00000137200 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs907205132 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109730,RMVar_hsa_circ_853,RMVar_hsa_circ_238199,RMVar_hsa_circ_48730,RMVar_hsa_circ_31058,RMVar_hsa_circ_266856,RMVar_hsa_circ_26975 19723 RMVar_ID_19723 Human_SNP_ID_273465382 A-to-I Human chr6 + 37449135 37449135 37449135 GCTAATTTTTTAGACTTTTTTTTAGTAGAGACAGAGTCTTGCTGTGTTGCCCAGACTGGTCTTAA GCTAATTTTTTAGACTTTTTTTTAGTAGAGACGGAGTCTTGCTGTGTTGCCCAGACTGGTCTTAA A G CMTR1 Ensembl:ENSG00000137200 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs888921384 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109730,RMVar_hsa_circ_853,RMVar_hsa_circ_238199,RMVar_hsa_circ_48730,RMVar_hsa_circ_31058,RMVar_hsa_circ_266856,RMVar_hsa_circ_26975 19724 RMVar_ID_19724 Human_SNP_ID_273465465 A-to-I Human chr6 + 37449372 37449372 37449372 GTTCTGTCACCCAGGCTGGAGTGCAGTGGCGCAATCTCGGCTCACTGCAACCTCTACCTTCCGGA GTTCTGTCACCCAGGCTGGAGTGCAGTGGCGCGATCTCGGCTCACTGCAACCTCTACCTTCCGGA A G CMTR1 Ensembl:ENSG00000137200 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982139695 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109730,RMVar_hsa_circ_853,RMVar_hsa_circ_238199,RMVar_hsa_circ_48730,RMVar_hsa_circ_31058,RMVar_hsa_circ_266856,RMVar_hsa_circ_26975 19725 RMVar_ID_19725 Human_SNP_ID_273470089 A-to-I Human chr6 + 37468970 37468970 37468970 TCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGTGGATCACCTCAGGCCAGGAGCTTG TCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGTGGATCACCTCAGGCCAGGAGCTTG A G CMTR1 Ensembl:ENSG00000137200 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1458982209 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127015,RMVar_hsa_circ_238205,RMVar_hsa_circ_117748,RMVar_hsa_circ_238208,RMVar_hsa_circ_98062,RMVar_hsa_circ_343583,RMVar_hsa_circ_94229,RMVar_hsa_circ_83689,RMVar_hsa_circ_125925,RMVar_hsa_circ_238209,RMVar_hsa_circ_238210,RMVar_hsa_circ_102332,RMVar_hsa_circ_238212,RMVar_hsa_circ_238213,RMVar_hsa_circ_238214 19726 RMVar_ID_19726 Human_SNP_ID_273470278 A-to-I Human chr6 + 37469717 37469716 37469718 GCCTGGCTAGTTTTTGTATTTTTAGTAGAGACAGAGTTTTGCTATGTTGGTCAGTCTGGTCTCGA GCCTGGCTAGTTTTTGTATTTTTAGTAGAGAC__AGTTTTGCTATGTTGGTCAGTCTGGTCTCGA CAG C CMTR1 Ensembl:ENSG00000137200 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474299197 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_127015,RMVar_hsa_circ_238205,RMVar_hsa_circ_117748,RMVar_hsa_circ_238208,RMVar_hsa_circ_98062,RMVar_hsa_circ_343583,RMVar_hsa_circ_94229,RMVar_hsa_circ_83689,RMVar_hsa_circ_125925,RMVar_hsa_circ_238209,RMVar_hsa_circ_238210,RMVar_hsa_circ_102332,RMVar_hsa_circ_238212,RMVar_hsa_circ_238213,RMVar_hsa_circ_238214 19727 RMVar_ID_19727 Human_SNP_ID_273473669 A-to-I Human chr6 - 37483042 37483042 37483042 CCTAGTGTTCAAGCATGGCTTCCTGGCGGCCCAGGCCTTGCCTCCCTGGCCTGCTGGGGGGTTCC CCTAGTGTTCAAGCATGGCTTCCTGGCGGCCCCGGCCTTGCCTCCCTGGCCTGCTGGGGGGTTCC T G CCDC167 Ensembl:ENSG00000198937 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1479998831 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_664008,Human_RBP_ID_5122487,Human_RBP_ID_17663134,Human_RBP_ID_27097868 19728 RMVar_ID_19728 Human_SNP_ID_273570590 A-to-I Human chr6 + 37866029 37866029 37866029 CCTCACTGCTGTAGAGATGGAGGTCTCACTATATTGTCCCGGCTGGTCTCAAATTCTTGGCCTTA CCTCACTGCTGTAGAGATGGAGGTCTCACTATGTTGTCCCGGCTGGTCTCAAATTCTTGGCCTTA A G ZFAND3 Ensembl:ENSG00000156639 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1034773816 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15817887,Human_RBP_ID_21338500 RMVar_hsa_circ_88011,RMVar_hsa_circ_238229 19729 RMVar_ID_19729 Human_SNP_ID_273571769 A-to-I Human chr6 + 37870720 37870720 37870720 TTTTGTGAATGAATGAGACAGGGTCTTGTTCTATTGCTCAGGCTAGAGGGCAGTGGTGCGATTAT TTTTGTGAATGAATGAGACAGGGTCTTGTTCTGTTGCTCAGGCTAGAGGGCAGTGGTGCGATTAT A G ZFAND3 Ensembl:ENSG00000156639 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569744931 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7602856,Human_RBP_ID_17576328 RMVar_hsa_circ_88011,RMVar_hsa_circ_238229 19730 RMVar_ID_19730 Human_SNP_ID_273571770 A-to-I Human chr6 + 37870720 37870720 37870720 TTTTGTGAATGAATGAGACAGGGTCTTGTTCTATTGCTCAGGCTAGAGGGCAGTGGTGCGATTAT TTTTGTGAATGAATGAGACAGGGTCTTGTTCTTTTGCTCAGGCTAGAGGGCAGTGGTGCGATTAT A T ZFAND3 Ensembl:ENSG00000156639 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569744931 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7602856,Human_RBP_ID_17576328 RMVar_hsa_circ_88011,RMVar_hsa_circ_238229 19731 RMVar_ID_19731 Human_SNP_ID_273572805 A-to-I Human chr6 + 37874809 37874809 37874809 TGTTGCCCAGGCTGGTCTCAAACTCTGGACTCAAGCAGTCCTCTCGCCTCAGCCTCCCAAAGTGC TGTTGCCCAGGCTGGTCTCAAACTCTGGACTCGAGCAGTCCTCTCGCCTCAGCCTCCCAAAGTGC A G ZFAND3 Ensembl:ENSG00000156639 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs776551879 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3006471,Human_RBP_ID_15818083 RMVar_hsa_circ_88011,RMVar_hsa_circ_238229 19732 RMVar_ID_19732 Human_SNP_ID_273590677 A-to-I Human chr6 + 37945618 37945618 37945618 TCTAGTCTCGAACTCCTGAACTCCAGTGATCCACCTGCCTTGGCCTCCCAAAGTGTTAGGATTAT TCTAGTCTCGAACTCCTGAACTCCAGTGATCCCCCTGCCTTGGCCTCCCAAAGTGTTAGGATTAT A C ZFAND3 Ensembl:ENSG00000156639 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1209183390 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15819285 RMVar_hsa_circ_19039,RMVar_hsa_circ_88011,RMVar_hsa_circ_372921,RMVar_hsa_circ_238229,RMVar_hsa_circ_342458,RMVar_hsa_circ_238230 19733 RMVar_ID_19733 Human_SNP_ID_273598226 A-to-I Human chr6 + 37976499 37976499 37976499 CCAGCTACTTGGGAGGCTGAGGTGGAAGAATCACTTGAGCCCCGGAAGTAGAGGTTGCAGTGAGC CCAGCTACTTGGGAGGCTGAGGTGGAAGAATCGCTTGAGCCCCGGAAGTAGAGGTTGCAGTGAGC A G ZFAND3 Ensembl:ENSG00000156639 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs543146668 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7603595,Human_RBP_ID_15819768 RMVar_hsa_circ_19039,RMVar_hsa_circ_88011,RMVar_hsa_circ_372921,RMVar_hsa_circ_238229,RMVar_hsa_circ_342458,RMVar_hsa_circ_238230 19734 RMVar_ID_19734 Human_SNP_ID_273604309 A-to-I Human chr6 + 38000697 38000697 38000697 GTAGGAATTATTCTCTAGTAAAACAATAAATTAGATCAAGGATGCTAAACTCTGTATTCACCTAA GTAGGAATTATTCTCTAGTAAAACAATAAATTCGATCAAGGATGCTAAACTCTGTATTCACCTAA A C ZFAND3 Ensembl:ENSG00000156639 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs914736361 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19039,RMVar_hsa_circ_88011,RMVar_hsa_circ_372921,RMVar_hsa_circ_238229,RMVar_hsa_circ_342458,RMVar_hsa_circ_238230 19735 RMVar_ID_19735 Human_SNP_ID_273604310 A-to-I Human chr6 + 38000697 38000697 38000697 GTAGGAATTATTCTCTAGTAAAACAATAAATTAGATCAAGGATGCTAAACTCTGTATTCACCTAA GTAGGAATTATTCTCTAGTAAAACAATAAATTTGATCAAGGATGCTAAACTCTGTATTCACCTAA A T ZFAND3 Ensembl:ENSG00000156639 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs914736361 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19039,RMVar_hsa_circ_88011,RMVar_hsa_circ_372921,RMVar_hsa_circ_238229,RMVar_hsa_circ_342458,RMVar_hsa_circ_238230 19736 RMVar_ID_19736 Human_SNP_ID_273620314 A-to-I Human chr6 + 38062557 38062556 38062558 GGTGCCTGCCACCATGCCTGGCTAATTAGTAGAAACAGGATCTCACCATGTTGGCCAAGCTGGTC GGTGCCTGCCACCATGCCTGGCTAATTAGTAG__ACAGGATCTCACCATGTTGGCCAAGCTGGTC GAA G ZFAND3 Ensembl:ENSG00000156639 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334186726 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_19039,RMVar_hsa_circ_88011,RMVar_hsa_circ_372921,RMVar_hsa_circ_238229,RMVar_hsa_circ_238230,RMVar_hsa_circ_321294,RMVar_hsa_circ_319457,RMVar_hsa_circ_238232 19737 RMVar_ID_19737 Human_SNP_ID_273630151 A-to-I Human chr6 + 38103271 38103271 38103271 TGGCTTTGTTATATGTTGTTTTCCTTAAAGTCACAGTTTCTAAGAGCCTGTCAGCAACATTGAGG TGGCTTTGTTATATGTTGTTTTCCTTAAAGTCGCAGTTTCTAAGAGCCTGTCAGCAACATTGAGG A G ZFAND3 Ensembl:ENSG00000156639 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1321184426 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88011,RMVar_hsa_circ_372921,RMVar_hsa_circ_238229,RMVar_hsa_circ_95998,RMVar_hsa_circ_238230,RMVar_hsa_circ_321294,RMVar_hsa_circ_238232,RMVar_hsa_circ_277308,RMVar_hsa_circ_238238,RMVar_hsa_circ_238239 19738 RMVar_ID_19738 Human_SNP_ID_273634803 A-to-I Human chr6 + 38121265 38121265 38121265 AGGCAAGATGGTGCAACCCTGTGGTCCCAGCTACTTGGGAGGCCAAGGTGGGAGGATGGCTTTCA AGGCAAGATGGTGCAACCCTGTGGTCCCAGCTGCTTGGGAGGCCAAGGTGGGAGGATGGCTTTCA A G ZFAND3 Ensembl:ENSG00000156639 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1267626774 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17576330 RMVar_hsa_circ_95998,RMVar_hsa_circ_238239 19739 RMVar_ID_19739 Human_SNP_ID_273634813 A-to-I Human chr6 + 38121302 38121302 38121302 GGAGGCCAAGGTGGGAGGATGGCTTTCAGCCCAGGAGTTCGAGGCTACAGTGAGTCTTGGTCACA GGAGGCCAAGGTGGGAGGATGGCTTTCAGCCCGGGAGTTCGAGGCTACAGTGAGTCTTGGTCACA A G ZFAND3 Ensembl:ENSG00000156639 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1231304692 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95998,RMVar_hsa_circ_238239 19740 RMVar_ID_19740 Human_SNP_ID_273701335 A-to-I Human chr6 - 38397039 38397039 38397039 AAATTAGCCAGGTGGGGTGGTGCACACCTGTAATCCCTGCTACTTGGGAAGCTGAGGCCTGAGAA AAATTAGCCAGGTGGGGTGGTGCACACCTGTAGTCCCTGCTACTTGGGAAGCTGAGGCCTGAGAA T C BTBD9 Ensembl:ENSG00000183826 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1234156401 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67243 19741 RMVar_ID_19741 Human_SNP_ID_273713334 A-to-I Human chr6 - 38448719 38448719 38448719 GAGGCCAGGAGTTGGAAACCAACCTGGCCAACATGGCAAAACCCCGTCTCTACTAAAAGTACAAA GAGGCCAGGAGTTGGAAACCAACCTGGCCAACGTGGCAAAACCCCGTCTCTACTAAAAGTACAAA T C BTBD9 Ensembl:ENSG00000183826 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569338392 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67243 19742 RMVar_ID_19742 Human_SNP_ID_273716730 A-to-I Human chr6 - 38463884 38463884 38463884 GGGACCACAGGAATATGCCACCATGCCTGGCTAATTTTTGTATTTTTTGTAGAGATGGGATTTCG GGGACCACAGGAATATGCCACCATGCCTGGCTGATTTTTGTATTTTTTGTAGAGATGGGATTTCG T C BTBD9 Ensembl:ENSG00000183826 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs548964728 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_1739 RMVar_hsa_circ_67243 19743 RMVar_ID_19743 Human_SNP_ID_273717571 A-to-I Human chr6 - 38466432 38466432 38466432 GCAAAATTAGTCAGGCGTAGTGATACATGCCTATAGTCTCAGCTACTCGGGAAGCTGACGCAGGA GCAAAATTAGTCAGGCGTAGTGATACATGCCTGTAGTCTCAGCTACTCGGGAAGCTGACGCAGGA T C BTBD9 Ensembl:ENSG00000183826 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1445200529 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67243 19744 RMVar_ID_19744 Human_SNP_ID_273728279 A-to-I Human chr6 - 38513263 38513223 38513264 TTTTGTATTTTTAGTAGAGACGGGGTTTCACCACGTTGATCAGGCTGGTCTGGAACTCCTGATCC TTTTGTATTTTTAGTAGAGACGGGGTTTCAC__________________________________ AGGGGAGTGGATCAGGAGTTCCAGACCAGCCTGATCAACGTG A BTBD9 Ensembl:ENSG00000183826 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1203258133 Functional Loss DEL dbSNP153 32..65 33 - - - RMVar_hsa_circ_67243 19745 RMVar_ID_19745 Human_SNP_ID_273728305 A-to-I Human chr6 - 38513326 38513326 38513326 CTTCTGCTTCAGCCTCCCAAGTAGCTGGGACTATAGGCATGCACCACCATGCCCGGCTAATTTTT CTTCTGCTTCAGCCTCCCAAGTAGCTGGGACTGTAGGCATGCACCACCATGCCCGGCTAATTTTT T C BTBD9 Ensembl:ENSG00000183826 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1316389946 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67243 19746 RMVar_ID_19746 Human_SNP_ID_273735487 A-to-I Human chr6 - 38545121 38545121 38545121 CGCCTCCACACTCCAGCCTGGGAGACAGTGCAAGACTCTGTCTCAAAAAACAAACAAACAAACAA CGCCTCCACACTCCAGCCTGGGAGACAGTGCACGACTCTGTCTCAAAAAACAAACAAACAAACAA T G BTBD9 Ensembl:ENSG00000183826 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs964945842 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67243 19747 RMVar_ID_19747 Human_SNP_ID_273735965 A-to-I Human chr6 - 38546871 38546871 38546871 CTGAGGTCGGGAGTTCGAGACCAGTCTGACCAACATGATGAAACCCCATCTCTACTAAAAATACA CTGAGGTCGGGAGTTCGAGACCAGTCTGACCAGCATGATGAAACCCCATCTCTACTAAAAATACA T C BTBD9 Ensembl:ENSG00000183826 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1257423023 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67243 19748 RMVar_ID_19748 Human_SNP_ID_273735984 A-to-I Human chr6 - 38546933 38546933 38546933 GCTGATTGCAGTGGCTCATGCCTGTAATCCCAACACTTGGGAGGCTGAGGTGGGTGGATCGCCTG GCTGATTGCAGTGGCTCATGCCTGTAATCCCAGCACTTGGGAGGCTGAGGTGGGTGGATCGCCTG T C BTBD9 Ensembl:ENSG00000183826 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1463476668 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67243 19749 RMVar_ID_19749 Human_SNP_ID_273740158 A-to-I Human chr6 - 38564770 38564770 38564770 CTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGTGCCTACCACCACGCCCAGCTAATTTTG CTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTGCAGGTGCCTACCACCACGCCCAGCTAATTTTG T C BTBD9 Ensembl:ENSG00000183826 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1197576365 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67243 19750 RMVar_ID_19750 Human_SNP_ID_273745146 A-to-I Human chr6 - 38587568 38587568 38587568 TTAACAAATAATGTCAATTTCAGTGTCCTACTACACTGAATTGCAAAGGAAAGATCAGAACTATC TTAACAAATAATGTCAATTTCAGTGTCCTACTGCACTGAATTGCAAAGGAAAGATCAGAACTATC T C BTBD9 Ensembl:ENSG00000183826 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1410564596 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67243,RMVar_hsa_circ_238244,RMVar_hsa_circ_238242,RMVar_hsa_circ_289446,RMVar_hsa_circ_282006,RMVar_hsa_circ_238246,RMVar_hsa_circ_238247,RMVar_hsa_circ_238245 19751 RMVar_ID_19751 Human_SNP_ID_273745150 A-to-I Human chr6 - 38587584 38587584 38587584 GGGTCTTCGTTGGCCATTAACAAATAATGTCAATTTCAGTGTCCTACTACACTGAATTGCAAAGG GGGTCTTCGTTGGCCATTAACAAATAATGTCAGTTTCAGTGTCCTACTACACTGAATTGCAAAGG T C BTBD9 Ensembl:ENSG00000183826 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs888856244 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67243,RMVar_hsa_circ_238244,RMVar_hsa_circ_238242,RMVar_hsa_circ_289446,RMVar_hsa_circ_282006,RMVar_hsa_circ_238246,RMVar_hsa_circ_238247,RMVar_hsa_circ_238245 19752 RMVar_ID_19752 Human_SNP_ID_273765502 A-to-I Human chr6 - 38676689 38676689 38676689 TTTATTTGGGAAAGGGGAGGAGGAAGGAAATGATATGGTACCCAGACACTGGGCTAGGCTGCAAC TTTATTTGGGAAAGGGGAGGAGGAAGGAAATGGTATGGTACCCAGACACTGGGCTAGGCTGCAAC T C GLO1 Ensembl:ENSG00000124767 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1487752678 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_664131,Human_RBP_ID_790195,Human_RBP_ID_1047519,Human_RBP_ID_2020970,Human_RBP_ID_4888820,Human_RBP_ID_7605012,Human_RBP_ID_10313945,Human_RBP_ID_15822376,Human_RBP_ID_17069930,Human_RBP_ID_17308949,Human_RBP_ID_17420102,Human_RBP_ID_17536156,Human_RBP_ID_17664083,Human_RBP_ID_18076138,Human_RBP_ID_18371178,Human_RBP_ID_23069220,Human_RBP_ID_24162323,Human_RBP_ID_26005612,Human_RBP_ID_26536567,Human_RBP_ID_26715484,Human_RBP_ID_27097939,Human_RBP_ID_27755901 Human_miRNA_ID_1788943,Human_miRNA_ID_2174790,Human_miRNA_ID_2178233 RMVar_hsa_circ_108768,RMVar_hsa_circ_238253 19753 RMVar_ID_19753 Human_SNP_ID_273766627 A-to-I Human chr6 - 38681201 38681201 38681201 AAAATTAGCCAGGCATGGTGGTGGGCGCCTATAGTCCGCCTACTCAGGAGGCTGAGGCAGGAGAA AAAATTAGCCAGGCATGGTGGTGGGCGCCTATTGTCCGCCTACTCAGGAGGCTGAGGCAGGAGAA T A GLO1 Ensembl:ENSG00000124767 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1266083460 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108768,RMVar_hsa_circ_238253 19754 RMVar_ID_19754 Human_SNP_ID_273766651 A-to-I Human chr6 - 38681291 38681291 38681291 TTGGGAGGCCAAGGCGGGCGGATCACGAGGTCAGGAGATCCAGACCATCTGGGCTAACATGGTGA TTGGGAGGCCAAGGCGGGCGGATCACGAGGTCTGGAGATCCAGACCATCTGGGCTAACATGGTGA T A GLO1 Ensembl:ENSG00000124767 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs996230174 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108768,RMVar_hsa_circ_238253 19755 RMVar_ID_19755 Human_SNP_ID_273769731 A-to-I Human chr6 - 38694619 38694619 38694619 GCTGGAGTGCAGTGGTGCCGTCTCAGCTCACTACAATCTCTGCTTCCCGGGTTCAAGGGCTCCTC GCTGGAGTGCAGTGGTGCCGTCTCAGCTCACTGCAATCTCTGCTTCCCGGGTTCAAGGGCTCCTC T C GLO1 Ensembl:ENSG00000124767 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1051672703 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108768,RMVar_hsa_circ_238253 19756 RMVar_ID_19756 Human_SNP_ID_273868117 A-to-I Human chr6 - 39097974 39097974 39097974 CTATTGGGAGGCTGAGGCATGGGAATCACTTGAACCTGGGAGGTGGAGGTTGCAGTGAGCCGAGA CTATTGGGAGGCTGAGGCATGGGAATCACTTGGACCTGGGAGGTGGAGGTTGCAGTGAGCCGAGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956578514 Functional Loss SNV dbSNP153 33..33 33 - - - 19757 RMVar_ID_19757 Human_SNP_ID_274072443 A-to-I Human chr6 + 39958799 39958799 39958799 CTACCAGAAGACCCAAGGAAATCTGGAATTTCACACCAGAGGACCCACCACGTCCTCGCTTCAAC CTACCAGAAGACCCAAGGAAATCTGGAATTTCGCACCAGAGGACCCACCACGTCCTCGCTTCAAC A G TUBBP9 Ensembl:ENSG00000220586 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878967621 Functional Loss SNV dbSNP153 33..33 33 - - - 19758 RMVar_ID_19758 Human_SNP_ID_274072453 A-to-I Human chr6 + 39958829 39958829 39958829 TCACACCAGAGGACCCACCACGTCCTCGCTTCAACATCTTGAAAGCCGGAAAGAAGAAAAAAGCA TCACACCAGAGGACCCACCACGTCCTCGCTTCGACATCTTGAAAGCCGGAAAGAAGAAAAAAGCA A G TUBBP9 Ensembl:ENSG00000220586 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879125529 Functional Loss SNV dbSNP153 33..33 33 - - - 19759 RMVar_ID_19759 Human_SNP_ID_274543888 A-to-I Human chr6 - 41820885 41820885 41820885 TCAATCCTCCCATGTCAGTCTCCCGAGTAGCTAGGACTACAGGCACATGCCACTACACCCAGATA TCAATCCTCCCATGTCAGTCTCCCGAGTAGCTGGGACTACAGGCACATGCCACTACACCCAGATA T C USP49 Ensembl:ENSG00000164663 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170060503 Functional Loss SNV dbSNP153 33..33 33 - - - 19760 RMVar_ID_19760 Human_SNP_ID_274551868 A-to-I Human chr6 - 41856184 41856184 41856184 TATTTTTAGTAGAGACAGGGTTTCACCATGTTAGCGAGGATGGTCTCGATCTCCTGACCTTGTGA TATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCGAGGATGGTCTCGATCTCCTGACCTTGTGA T C USP49 Ensembl:ENSG00000164663 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1561919496 Functional Loss SNV dbSNP153 33..33 33 - - - 19761 RMVar_ID_19761 Human_SNP_ID_274554165 A-to-I Human chr6 - 41866060 41866060 41866060 AAAATTGGTGGGACGTGGTGGTGGGCGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGGAGGAGA AAAATTGGTGGGACGTGGTGGTGGGCGCCTGTTGTCCCAGCTACTTGGGAGGCTGAGGGAGGAGA T A USP49 Ensembl:ENSG00000164663 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1561922376 Functional Loss SNV dbSNP153 33..33 33 - - - 19762 RMVar_ID_19762 Human_SNP_ID_274569203 A-to-I Human chr6 + 41929091 41929091 41929091 GCCTGGCTAATTTTTGTTTTATTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTCAA GCCTGGCTAATTTTTGTTTTATTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGGTCTCAA A G BYSL Ensembl:ENSG00000112578 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs948635420 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109180,RMVar_hsa_circ_98970,RMVar_hsa_circ_238332,RMVar_hsa_circ_238333 19763 RMVar_ID_19763 Human_SNP_ID_274569204 A-to-I Human chr6 + 41929091 41929091 41929091 GCCTGGCTAATTTTTGTTTTATTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTCAA GCCTGGCTAATTTTTGTTTTATTAGTAGAGACTGGGTTTCACCATGTTGGCCAGGCTGGTCTCAA A T BYSL Ensembl:ENSG00000112578 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs948635420 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109180,RMVar_hsa_circ_98970,RMVar_hsa_circ_238332,RMVar_hsa_circ_238333 19764 RMVar_ID_19764 Human_SNP_ID_274569258 A-to-I Human chr6 + 41929327 41929327 41929327 TGAGACCAGCCTGGGCAACATGGGGAGACCCCATCTCTACAGAAGAATAAAAAACTAGCTGGGCC TGAGACCAGCCTGGGCAACATGGGGAGACCCCGTCTCTACAGAAGAATAAAAAACTAGCTGGGCC A G BYSL Ensembl:ENSG00000112578 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1270533976 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109180,RMVar_hsa_circ_98970,RMVar_hsa_circ_238332,RMVar_hsa_circ_238333 19765 RMVar_ID_19765 Human_SNP_ID_274570602 A-to-I Human chr6 + 41933871 41933871 41933871 TCGGCTCGCTGCAACCTCCGCCTCCATGGTTCAAGAGATTCTCCTGCCTCAGCCTCCTGAGTAGC TCGGCTCGCTGCAACCTCCGCCTCCATGGTTCGAGAGATTCTCCTGCCTCAGCCTCCTGAGTAGC A G RF00017-4499,RF00017-4494 RNACentral:URS000098B860,RNACentral:URS00009086DB SRP RNA,SRP RNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1435111773 Functional Loss SNV dbSNP153 33..33 33 - - - 19766 RMVar_ID_19766 Human_SNP_ID_274583460 A-to-I Human chr6 - 41985488 41985488 41985488 CAACATGGTGAAACCCCGTCTCTATTAAAAATACACAAAATTAGCCAGGTGTGGTGGTGGACACC CAACATGGTGAAACCCCGTCTCTATTAAAAATGCACAAAATTAGCCAGGTGTGGTGGTGGACACC T C CCND3 Ensembl:ENSG00000112576 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs537812361 Functional Loss SNV dbSNP153 33..33 33 - - - 19767 RMVar_ID_19767 Human_SNP_ID_274583753 A-to-I Human chr6 - 41986727 41986725 41986728 CAAATAAATGGCATCCAAATTGGAAAAGAAGAAGTAACATTGTCTCTGCAGATGACATGATCGTA CAAATAAATGGCATCCAAATTGGAAAAGAAG___TAACATTGTCTCTGCAGATGACATGATCGTA ACTT A CCND3 Ensembl:ENSG00000112576 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1445850394 Functional Loss DEL dbSNP153 32..34 33 - - - 19768 RMVar_ID_19768 Human_SNP_ID_274584130 A-to-I Human chr6 - 41987774 41987774 41987774 TCCGTGGCCTGTCATGCTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGAAGA TCCGTGGCCTGTCATGCTGGCTCACACCTGTATTCCCAGCACTTTGGGAGGCCAAGGCAGGAAGA T A CCND3 Ensembl:ENSG00000112576 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs550085092 Functional Loss SNV dbSNP153 33..33 33 - - - 19769 RMVar_ID_19769 Human_SNP_ID_274584131 A-to-I Human chr6 - 41987781 41987781 41987781 AAAAAATTCCGTGGCCTGTCATGCTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGC AAAAAATTCCGTGGCCTGTCATGCTGGCTCACCCCTGTAATCCCAGCACTTTGGGAGGCCAAGGC T G CCND3 Ensembl:ENSG00000112576 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1425111148 Functional Loss SNV dbSNP153 33..33 33 - - - 19770 RMVar_ID_19770 Human_SNP_ID_274596340 A-to-I Human chr6 - 42036677 42036677 42036677 AGGACTGGCCAGGCACAGTGGCTCATGCCTGTAATCTCAGCACTTTGGGAGGCCAAGGCGGGCAG AGGACTGGCCAGGCACAGTGGCTCATGCCTGTGATCTCAGCACTTTGGGAGGCCAAGGCGGGCAG T C CCND3 Ensembl:ENSG00000112576 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1295466689 Functional Loss SNV dbSNP153 33..33 33 - - - 19771 RMVar_ID_19771 Human_SNP_ID_274596650 A-to-I Human chr6 - 42037811 42037811 42037811 GGTCAGACTAGTCTTGAACTCCTGACCTCATGATCCGTCCGCCTCGGCCTCCCAAAGTGCTGTGA GGTCAGACTAGTCTTGAACTCCTGACCTCATGTTCCGTCCGCCTCGGCCTCCCAAAGTGCTGTGA T A CCND3 Ensembl:ENSG00000112576 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1265407713 Functional Loss SNV dbSNP153 33..33 33 - - - 19772 RMVar_ID_19772 Human_SNP_ID_274598030 A-to-I Human chr6 - 42043692 42043692 42043692 AATGAGCAAGGACACCCTGATTTTTTTGAGACAGGGTCTCACTCTGTCGCCCAGGCTGGAGTGCA AATGAGCAAGGACACCCTGATTTTTTTGAGACGGGGTCTCACTCTGTCGCCCAGGCTGGAGTGCA T C CCND3 Ensembl:ENSG00000112576 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs966527300 Functional Loss SNV dbSNP153 33..33 33 - - - 19773 RMVar_ID_19773 Human_SNP_ID_274602037 A-to-I Human chr6 + 42058277 42058277 42058277 GTGGTGGCACATACCTGTAGTTCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCTAACCTGGGAG GTGGTGGCACATACCTGTAGTTCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCTAACCTGGGAG A G TAF8 Ensembl:ENSG00000137413 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1342878053 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34252,RMVar_hsa_circ_64717,RMVar_hsa_circ_113407,RMVar_hsa_circ_238343 19774 RMVar_ID_19774 Human_SNP_ID_274606947 A-to-I Human chr6 + 42077792 42077792 42077792 TTTTTTTTTATTTTGAGATGGAGTCTTACTCTATCACCCAGGCTGGAATGCAGTGGTGTGATCTC TTTTTTTTTATTTTGAGATGGAGTCTTACTCTGTCACCCAGGCTGGAATGCAGTGGTGTGATCTC A G TAF8 Ensembl:ENSG00000137413 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs188083067 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26539470 RMVar_hsa_circ_105984,RMVar_hsa_circ_238347 19775 RMVar_ID_19775 Human_SNP_ID_274606983 A-to-I Human chr6 + 42077939 42077939 42077939 CCACCATGCTGGCTAATTTTTGTATTTTGAGTAGAGATAGGGTTTCGCCATGTTGGCCAGGCTGG CCACCATGCTGGCTAATTTTTGTATTTTGAGTGGAGATAGGGTTTCGCCATGTTGGCCAGGCTGG A G TAF8 Ensembl:ENSG00000137413 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1465202603 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_170039 RMVar_hsa_circ_105984,RMVar_hsa_circ_238347 19776 RMVar_ID_19776 Human_SNP_ID_274607413 A-to-I Human chr6 + 42079637 42079637 42079637 CCAGCTGGAGTATAGTGGCACTACCTCGGCTCACTGCAACCTCCACTCCCCGGGTTCAAGCAATT CCAGCTGGAGTATAGTGGCACTACCTCGGCTCGCTGCAACCTCCACTCCCCGGGTTCAAGCAATT A G TAF8 Ensembl:ENSG00000137413 Protein coding intron GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,29796672,31158229,31158229,31158229,32596459 RNA-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 19777 RMVar_ID_19777 Human_SNP_ID_274607454 A-to-I Human chr6 + 42079754 42079754 42079754 TTTTTTTTTTTTAGTAGACACGGGATTTTGCTATGTTGCCCAGGCTGGTCTTGAACTCCTGGCCT TTTTTTTTTTTTAGTAGACACGGGATTTTGCTGTGTTGCCCAGGCTGGTCTTGAACTCCTGGCCT A G TAF8 Ensembl:ENSG00000137413 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs572101523 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4889873,Human_RBP_ID_22372220,Human_RBP_ID_26539482 Human_miRNA_ID_1142343,Human_miRNA_ID_1159589 RMVar_hsa_circ_105984,RMVar_hsa_circ_238347 19778 RMVar_ID_19778 Human_SNP_ID_274607664 A-to-I Human chr6 + 42080538 42080538 42080538 GGGATTACAGGCACCTACCACAATTCTCGGCTAATTTTTTTTGTATTTTTGGTAGAGACGGGGTT GGGATTACAGGCACCTACCACAATTCTCGGCTGATTTTTTTTGTATTTTTGGTAGAGACGGGGTT A G TAF8 Ensembl:ENSG00000137413 Protein coding intron GSE38233;GSE100210;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1368262132 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7606891 RMVar_hsa_circ_105984,RMVar_hsa_circ_238347 19779 RMVar_ID_19779 Human_SNP_ID_274607685 A-to-I Human chr6 + 42080610 42080610 42080610 GTTGGCCAGGGTGGTCTCGAACACCTGACCTCAGATGATCCACCCACCTCGGCCTCCCAGTGTGG GTTGGCCAGGGTGGTCTCGAACACCTGACCTCGGATGATCCACCCACCTCGGCCTCCCAGTGTGG A G TAF8 Ensembl:ENSG00000137413 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1014756987 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5151916,Human_RBP_ID_26540147 RMVar_hsa_circ_105984,RMVar_hsa_circ_238347 19780 RMVar_ID_19780 Human_SNP_ID_274607692 A-to-I Human chr6 + 42080636 42080636 42080636 GACCTCAGATGATCCACCCACCTCGGCCTCCCAGTGTGGGTGGGATTACAGGCATGAGCCACCGC GACCTCAGATGATCCACCCACCTCGGCCTCCCGGTGTGGGTGGGATTACAGGCATGAGCCACCGC A G TAF8 Ensembl:ENSG00000137413 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs970329121 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26540148 RMVar_hsa_circ_105984,RMVar_hsa_circ_238347 19781 RMVar_ID_19781 Human_SNP_ID_274608517 A-to-I Human chr6 + 42083932 42083932 42083932 TGCTGGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCAGAGGCGGGCGGATCACG TGCTGGGCACGGTGGCTCACGCCTGTAATCCCGGCACTTTGGGAGGCAGAGGCGGGCGGATCACG A G TAF8 Ensembl:ENSG00000137413 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1435255601 Functional Loss SNV dbSNP153 33..33 33 - - - 19782 RMVar_ID_19782 Human_SNP_ID_274608957 A-to-I Human chr6 + 42085567 42085567 42085567 CCTCTAGGCCAGGCGCGGTGGCTTATGCCTGCAATCCCAGTGCTTTGGGAGGCTGAGGCAGGAGG CCTCTAGGCCAGGCGCGGTGGCTTATGCCTGCTATCCCAGTGCTTTGGGAGGCTGAGGCAGGAGG A T TAF8 Ensembl:ENSG00000137413 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs941084480 Functional Loss SNV dbSNP153 33..33 33 - - - 19783 RMVar_ID_19783 Human_SNP_ID_274619641 A-to-I Human chr6 - 42126760 42126760 42126760 CGGCTCCCTGCAACCTCCACCTCCTGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCT CGGCTCCCTGCAACCTCCACCTCCTGGGTTCAGGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCT T C C6orf132 Ensembl:ENSG00000188112 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1347369994 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_769986 19784 RMVar_ID_19784 Human_SNP_ID_274619653 A-to-I Human chr6 - 42126804 42126804 42126804 TTCATTCTTGTTGCCCAGGCTGGAGTGGTACAATGGCGTGATCTCGGCTCCCTGCAACCTCCACC TTCATTCTTGTTGCCCAGGCTGGAGTGGTACAGTGGCGTGATCTCGGCTCCCTGCAACCTCCACC T C C6orf132 Ensembl:ENSG00000188112 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1479480078 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_769986 19785 RMVar_ID_19785 Human_SNP_ID_274636907 A-to-I Human chr6 - 42192137 42192137 42192137 GTTGGCCATGATTGTCTCCATCTCTTGACTTCATGATCCACCCGCCTCGGTCTCCCAAAGTGTTG GTTGGCCATGATTGTCTCCATCTCTTGACTTCGTGATCCACCCGCCTCGGTCTCCCAAAGTGTTG T C GUCA1B Ensembl:ENSG00000112599 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1175115300 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15827458 19786 RMVar_ID_19786 Human_SNP_ID_274639383 A-to-I Human chr6 - 42201075 42201075 42201075 AAACCTAGCCGGGCTTGCTGGCGGGTGCCTATAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAACCTAGCCGGGCTTGCTGGCGGGTGCCTATGGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA T C RF00017-4541 RNACentral:URS0000992647 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1468279177 Functional Loss SNV dbSNP153 33..33 33 - - - 19787 RMVar_ID_19787 Human_SNP_ID_274639385 A-to-I Human chr6 - 42201077 42201077 42201077 CAAAACCTAGCCGGGCTTGCTGGCGGGTGCCTATAGTCCCAGCTACTCGGGAGGCTGAGGCAGGA CAAAACCTAGCCGGGCTTGCTGGCGGGTGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGA T C RF00017-4541 RNACentral:URS0000992647 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1279706841 Functional Loss SNV dbSNP153 33..33 33 - - - 19788 RMVar_ID_19788 Human_SNP_ID_274639424 A-to-I Human chr6 - 42201201 42201201 42201201 TGGGTGTGGTCACTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGATGGGTGGATCACCTGA TGGGTGTGGTCACTCATGCCTGTAATCCCAGCGCTTTGGGAGGCTGAGATGGGTGGATCACCTGA T C RF00017-4541 RNACentral:URS0000992647 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs777519986 Functional Loss SNV dbSNP153 33..33 33 - - - 19789 RMVar_ID_19789 Human_SNP_ID_274639713 A-to-I Human chr6 - 42202362 42202362 42202362 CACCACGCCCAGCTAACTTTTGTATTTTTAGTAGAGATGGGGTTTCGGTGTGTTGGCCAGGCTGG CACCACGCCCAGCTAACTTTTGTATTTTTAGTGGAGATGGGGTTTCGGTGTGTTGGCCAGGCTGG T C RF00017-4541 RNACentral:URS0000992647 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs955071323 Functional Loss SNV dbSNP153 33..33 33 - - - 19790 RMVar_ID_19790 Human_SNP_ID_274640090 A-to-I Human chr6 - 42203780 42203780 42203780 CTTAGCGTTGTTTTTCAGACAGTTCTGGCTCTATCACCCAGGCTGGAGTGCAGTGACAATCTTGG CTTAGCGTTGTTTTTCAGACAGTTCTGGCTCTGTCACCCAGGCTGGAGTGCAGTGACAATCTTGG T C RF00017-4541 RNACentral:URS0000992647 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs967385490 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15827780 19791 RMVar_ID_19791 Human_SNP_ID_274640443 A-to-I Human chr6 - 42205140 42205140 42205140 AAGCTCACTACACAATCGAACTTATGGGCTCAAGGGATCTTCCCACCACAGCCTCCCAAGTAGCT AAGCTCACTACACAATCGAACTTATGGGCTCAGGGGATCTTCCCACCACAGCCTCCCAAGTAGCT T C RF00017-4541 RNACentral:URS0000992647 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1175591570 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15827815 19792 RMVar_ID_19792 Human_SNP_ID_274640451 A-to-I Human chr6 - 42205163 42205163 42205163 GCTGGAGTGCAGTGGTACGATCAAAGCTCACTACACAATCGAACTTATGGGCTCAAGGGATCTTC GCTGGAGTGCAGTGGTACGATCAAAGCTCACTGCACAATCGAACTTATGGGCTCAAGGGATCTTC T C RF00017-4541 RNACentral:URS0000992647 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1293823551 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15827817 19793 RMVar_ID_19793 Human_SNP_ID_274640736 A-to-I Human chr6 - 42206137 42206137 42206137 CGGCTCATTGCAACCTCTGCCTCCCAGGTTCAAGCGATTATCCTGCCTCAGCCTCCCAAGTAGCT CGGCTCATTGCAACCTCTGCCTCCCAGGTTCAGGCGATTATCCTGCCTCAGCCTCCCAAGTAGCT T C RF00017-4541 RNACentral:URS0000992647 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1269382377 Functional Loss SNV dbSNP153 33..33 33 - - - 19794 RMVar_ID_19794 Human_SNP_ID_274640896 A-to-I Human chr6 - 42206594 42206594 42206594 GACCCGGCCGGTTGTGGAGGCTCAAGCCTGTAATCCCAGCACTTTGAGAGGCTGAGGCAGGTGGA GACCCGGCCGGTTGTGGAGGCTCAAGCCTGTAGTCCCAGCACTTTGAGAGGCTGAGGCAGGTGGA T C RF00017-4541 RNACentral:URS0000992647 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs530560749 Functional Loss SNV dbSNP153 33..33 33 - - - 19795 RMVar_ID_19795 Human_SNP_ID_274641086 A-to-I Human chr6 - 42207390 42207390 42207390 CGGTGAAACCCCGTCTCTAATAAAAATACAAAAATTAGCTGGACATGGTGGCACGTGCCTGTAAT CGGTGAAACCCCGTCTCTAATAAAAATACAAATATTAGCTGGACATGGTGGCACGTGCCTGTAAT T A MRPS10 Ensembl:ENSG00000048544 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1014057003 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91348,RMVar_hsa_circ_117197,RMVar_hsa_circ_125393,RMVar_hsa_circ_113619,RMVar_hsa_circ_238352,RMVar_hsa_circ_83015,RMVar_hsa_circ_85196,RMVar_hsa_circ_238354,RMVar_hsa_circ_81962,RMVar_hsa_circ_238355,RMVar_hsa_circ_238353,RMVar_hsa_circ_238350,RMVar_hsa_circ_238351,RMVar_hsa_circ_238349 19796 RMVar_ID_19796 Human_SNP_ID_274643412 A-to-I Human chr6 - 42216135 42216135 42216135 CCTGTAATCCCACCTACTCAGGAGGCTAAGGCAGGAGACTTGCTTGAACCCAGGAGGCGGAGGTT CCTGTAATCCCACCTACTCAGGAGGCTAAGGCGGGAGACTTGCTTGAACCCAGGAGGCGGAGGTT T C MRPS10 Ensembl:ENSG00000048544 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749601122 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125393,RMVar_hsa_circ_238355 19797 RMVar_ID_19797 Human_SNP_ID_274643696 A-to-I Human chr6 - 42216645 42216645 42216645 CACCATGCCCAGCTAGTATTTGTATGTTTAGCAGAGACGGGGTTTCACCATGTCGGTCAGGCTGG CACCATGCCCAGCTAGTATTTGTATGTTTAGCCGAGACGGGGTTTCACCATGTCGGTCAGGCTGG T G MRPS10 Ensembl:ENSG00000048544 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1185355931 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125393,RMVar_hsa_circ_238355 19798 RMVar_ID_19798 Human_SNP_ID_274656353 A-to-I Human chr6 - 42267218 42267218 42267218 ACGATCCTCCCACTTCACCCTCCCACATAGCTAGAACTACAGGTGCATGCCACCTGGGCCTGAGC ACGATCCTCCCACTTCACCCTCCCACATAGCTGGAACTACAGGTGCATGCCACCTGGGCCTGAGC T C TRERF1 Ensembl:ENSG00000124496 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1325336014 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_238357,RMVar_hsa_circ_123860,RMVar_hsa_circ_377231,RMVar_hsa_circ_329225 19799 RMVar_ID_19799 Human_SNP_ID_274656377 A-to-I Human chr6 - 42267328 42267328 42267328 CTGTGCCTGGCCCCTTTTTTCTTTTTTTAGACAGGGTCTTGCTCTGTCACCCAGGCTGGAATGCA CTGTGCCTGGCCCCTTTTTTCTTTTTTTAGACCGGGTCTTGCTCTGTCACCCAGGCTGGAATGCA T G TRERF1 Ensembl:ENSG00000124496 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1561866620 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7607200 RMVar_hsa_circ_238357,RMVar_hsa_circ_123860,RMVar_hsa_circ_377231,RMVar_hsa_circ_329225 19800 RMVar_ID_19800 Human_SNP_ID_274668891 A-to-I Human chr6 - 42318097 42318097 42318097 CAGACTAGAGTGTAGTGGGGTGATCTCGGCTTACTACAACCTCCACCTCCCAAGTTCAAGCGATT CAGACTAGAGTGTAGTGGGGTGATCTCGGCTTGCTACAACCTCCACCTCCCAAGTTCAAGCGATT T C TRERF1 Ensembl:ENSG00000124496 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs796381928 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_171705 RMVar_hsa_circ_11291 19801 RMVar_ID_19801 Human_SNP_ID_274731585 A-to-I Human chr6 + 42579571 42579571 42579571 TTGAGACAGAGTCCCATTCTGTCGCTTAGTCTAGAGTACAGTGGCATGATCATAACTCACTGCAG TTGAGACAGAGTCCCATTCTGTCGCTTAGTCTGGAGTACAGTGGCATGATCATAACTCACTGCAG A G UBR2 Ensembl:ENSG00000024048 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1036769366 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113282,RMVar_hsa_circ_336982,RMVar_hsa_circ_369964,RMVar_hsa_circ_346645,RMVar_hsa_circ_296455,RMVar_hsa_circ_122541,RMVar_hsa_circ_238369,RMVar_hsa_circ_238373,RMVar_hsa_circ_75952,RMVar_hsa_circ_90155,RMVar_hsa_circ_238375,RMVar_hsa_circ_238374,RMVar_hsa_circ_238371,RMVar_hsa_circ_238372,RMVar_hsa_circ_238370,RMVar_hsa_circ_238368 19802 RMVar_ID_19802 Human_SNP_ID_274738929 A-to-I Human chr6 + 42611724 42611724 42611724 GGTCAGGAGTTCAAGACCAGCCTGGCTAACATAGTGAAACCCTGTCTCTACTAAAAATACAACAG GGTCAGGAGTTCAAGACCAGCCTGGCTAACATGGTGAAACCCTGTCTCTACTAAAAATACAACAG A G UBR2 Ensembl:ENSG00000024048 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1432866146 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5585,RMVar_hsa_circ_113282,RMVar_hsa_circ_369964,RMVar_hsa_circ_122541,RMVar_hsa_circ_238369,RMVar_hsa_circ_75952,RMVar_hsa_circ_90155,RMVar_hsa_circ_238371,RMVar_hsa_circ_238372,RMVar_hsa_circ_238370,RMVar_hsa_circ_362767,RMVar_hsa_circ_371446,RMVar_hsa_circ_238368,RMVar_hsa_circ_363664,RMVar_hsa_circ_95822,RMVar_hsa_circ_3363,RMVar_hsa_circ_16453,RMVar_hsa_circ_73795,RMVar_hsa_circ_118574,RMVar_hsa_circ_238379,RMVar_hsa_circ_238380,RMVar_hsa_circ_374678,RMVar_hsa_circ_337378,RMVar_hsa_circ_106631,RMVar_hsa_circ_100631,RMVar_hsa_circ_61482,RMVar_hsa_circ_68726,RMVar_hsa_circ_24027,RMVar_hsa_circ_11906,RMVar_hsa_circ_238389,RMVar_hsa_circ_238384,RMVar_hsa_circ_238386,RMVar_hsa_circ_238385,RMVar_hsa_circ_238382,RMVar_hsa_circ_238383,RMVar_hsa_circ_238381,RMVar_hsa_circ_71718,RMVar_hsa_circ_310171,RMVar_hsa_circ_346859,RMVar_hsa_circ_291921,RMVar_hsa_circ_275482,RMVar_hsa_circ_32012,RMVar_hsa_circ_48826,RMVar_hsa_circ_21242,RMVar_hsa_circ_52121,RMVar_hsa_circ_238392,RMVar_hsa_circ_238393,RMVar_hsa_circ_238394,RMVar_hsa_circ_54966,RMVar_hsa_circ_23658,RMVar_hsa_circ_43922,RMVar_hsa_circ_7153 19803 RMVar_ID_19803 Human_SNP_ID_274748518 A-to-I Human chr6 + 42647545 42647544 42647545 TTGGACCTGGAAGGTGGAGGTTGCAGTGAGCCAAGATCATGCCATTGCACTCCAGCCTGGGTAAC TTGGACCTGGAAGGTGGAGGTTGCAGTGAGCC_AGATCATGCCATTGCACTCCAGCCTGGGTAAC CA C UBR2 Ensembl:ENSG00000024048 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1190594617 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_1796,RMVar_hsa_circ_90155,RMVar_hsa_circ_238368,RMVar_hsa_circ_95822,RMVar_hsa_circ_16453,RMVar_hsa_circ_118574,RMVar_hsa_circ_238380,RMVar_hsa_circ_24027,RMVar_hsa_circ_238381,RMVar_hsa_circ_88379,RMVar_hsa_circ_106666,RMVar_hsa_circ_122510,RMVar_hsa_circ_112348,RMVar_hsa_circ_102779,RMVar_hsa_circ_238399,RMVar_hsa_circ_238397,RMVar_hsa_circ_238398,RMVar_hsa_circ_238396,RMVar_hsa_circ_37165,RMVar_hsa_circ_238409,RMVar_hsa_circ_28018,RMVar_hsa_circ_84919,RMVar_hsa_circ_238407,RMVar_hsa_circ_238408,RMVar_hsa_circ_49295,RMVar_hsa_circ_238414,RMVar_hsa_circ_238415,RMVar_hsa_circ_110395,RMVar_hsa_circ_24473,RMVar_hsa_circ_96320,RMVar_hsa_circ_238419,RMVar_hsa_circ_115499,RMVar_hsa_circ_101742,RMVar_hsa_circ_238420,RMVar_hsa_circ_6713,RMVar_hsa_circ_30739,RMVar_hsa_circ_48810,RMVar_hsa_circ_238424,RMVar_hsa_circ_86810,RMVar_hsa_circ_43991,RMVar_hsa_circ_238426,RMVar_hsa_circ_118813,RMVar_hsa_circ_238428,RMVar_hsa_circ_295831,RMVar_hsa_circ_310580,RMVar_hsa_circ_363554,RMVar_hsa_circ_308334,RMVar_hsa_circ_95734,RMVar_hsa_circ_238430,RMVar_hsa_circ_238432,RMVar_hsa_circ_19987,RMVar_hsa_circ_238433,RMVar_hsa_circ_238431,RMVar_hsa_circ_124423,RMVar_hsa_circ_238429,RMVar_hsa_circ_238434,RMVar_hsa_circ_238435 19804 RMVar_ID_19804 Human_SNP_ID_274754708 A-to-I Human chr6 + 42673421 42673421 42673421 TCAGCTCACTGCAACCTCTGCCTCCAGGGTTCAAGTGATTCTCCTTCCTCAGCCTCTCGAGTAGC TCAGCTCACTGCAACCTCTGCCTCCAGGGTTCGAGTGATTCTCCTTCCTCAGCCTCTCGAGTAGC A G UBR2 Ensembl:ENSG00000024048 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1401931387 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16453,RMVar_hsa_circ_88379,RMVar_hsa_circ_112348,RMVar_hsa_circ_102779,RMVar_hsa_circ_238397,RMVar_hsa_circ_238396,RMVar_hsa_circ_238407,RMVar_hsa_circ_238408,RMVar_hsa_circ_19508,RMVar_hsa_circ_60081,RMVar_hsa_circ_30495,RMVar_hsa_circ_109486,RMVar_hsa_circ_238444,RMVar_hsa_circ_45069,RMVar_hsa_circ_120767,RMVar_hsa_circ_19611,RMVar_hsa_circ_238450,RMVar_hsa_circ_336769,RMVar_hsa_circ_238456,RMVar_hsa_circ_321958,RMVar_hsa_circ_22119,RMVar_hsa_circ_238457,RMVar_hsa_circ_327504,RMVar_hsa_circ_76964,RMVar_hsa_circ_238462,RMVar_hsa_circ_64766,RMVar_hsa_circ_238461,RMVar_hsa_circ_23509,RMVar_hsa_circ_238464,RMVar_hsa_circ_50278,RMVar_hsa_circ_339425 19805 RMVar_ID_19805 Human_SNP_ID_274757569 A-to-I Human chr6 + 42685661 42685661 42685661 TAATTTTTTTTTTGTATTTTTAGTATCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAG TAATTTTTTTTTTGTATTTTTAGTATCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAG A G UBR2 Ensembl:ENSG00000024048 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs909266241 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112348,RMVar_hsa_circ_238396,RMVar_hsa_circ_109486,RMVar_hsa_circ_238444,RMVar_hsa_circ_120767,RMVar_hsa_circ_238450 19806 RMVar_ID_19806 Human_SNP_ID_274758335 A-to-I Human chr6 + 42687724 42687724 42687724 CACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATATTGGTCAGGCTGG CACCATGCCTGGCTAATTTTTGTATTTTTAGTGGAGACGGGGTTTCACCATATTGGTCAGGCTGG A G UBR2 Ensembl:ENSG00000024048 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1011425415 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112348,RMVar_hsa_circ_238396,RMVar_hsa_circ_109486,RMVar_hsa_circ_238444,RMVar_hsa_circ_120767,RMVar_hsa_circ_238450 19807 RMVar_ID_19807 Human_SNP_ID_274758341 A-to-I Human chr6 + 42687750 42687750 42687750 TTTAGTAGAGACGGGGTTTCACCATATTGGTCAGGCTGGTCTCAAACTCCTGACCTCAGTTGATC TTTAGTAGAGACGGGGTTTCACCATATTGGTCGGGCTGGTCTCAAACTCCTGACCTCAGTTGATC A G UBR2 Ensembl:ENSG00000024048 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1279711083 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112348,RMVar_hsa_circ_238396,RMVar_hsa_circ_109486,RMVar_hsa_circ_238444,RMVar_hsa_circ_120767,RMVar_hsa_circ_238450 19808 RMVar_ID_19808 Human_SNP_ID_274775493 A-to-I Human chr6 + 42753253 42753253 42753253 CTGGCCTGATTTTTAAATGTTTTTGTAGAGACAGGGTCTTGCTGTGTTGCCCAGTCTGGTCTTGA CTGGCCTGATTTTTAAATGTTTTTGTAGAGACGGGGTCTTGCTGTGTTGCCCAGTCTGGTCTTGA A G BICRAL Ensembl:ENSG00000112624 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985062288 Functional Loss SNV dbSNP153 33..33 33 - - - 19809 RMVar_ID_19809 Human_SNP_ID_274777535 A-to-I Human chr6 + 42761646 42761646 42761646 TATTTACTTCTTGGCTGGGCACAGTGGCTCATACTTGTAGTCCCAGAACTTTGGGAGGCTGAGGC TATTTACTTCTTGGCTGGGCACAGTGGCTCATGCTTGTAGTCCCAGAACTTTGGGAGGCTGAGGC A G BICRAL Ensembl:ENSG00000112624 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs895401808 Functional Loss SNV dbSNP153 33..33 33 - - - 19810 RMVar_ID_19810 Human_SNP_ID_274783529 A-to-I Human chr6 + 42785546 42785532 42785546 CCCCACCATTGCACTCCAGTCCGGGAAACAAGAACGAAACTCCCATCTCAAAAAAAAAAAAAAGA CCCCACCATTGCACTCCAG______________ACGAAACTCCCATCTCAAAAAAAAAAAAAAGA GTCCGGGAAACAAGA G BICRAL Ensembl:ENSG00000112624 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs552902992 Functional Loss DEL dbSNP153 20..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 19811 RMVar_ID_19811 Human_SNP_ID_274784361 A-to-I Human chr6 + 42788496 42788496 42788496 CACGCACCTAGGCCTCCCAAAATGTTGGGATTATAGGTGTGAGCCACCATGCCTGGCCGGGAGCA CACGCACCTAGGCCTCCCAAAATGTTGGGATTGTAGGTGTGAGCCACCATGCCTGGCCGGGAGCA A G BICRAL Ensembl:ENSG00000112624 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1425411805 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 19812 RMVar_ID_19812 Human_SNP_ID_274784612 A-to-I Human chr6 + 42789535 42789535 42789535 ATGGTGGCACACACCTGTAATCCCAGCTACTCAGGAGGCTGAGGCATGAGAATTGCTTGAACCTG ATGGTGGCACACACCTGTAATCCCAGCTACTCGGGAGGCTGAGGCATGAGAATTGCTTGAACCTG A G BICRAL Ensembl:ENSG00000112624 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1011346700 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 19813 RMVar_ID_19813 Human_SNP_ID_274784793 A-to-I Human chr6 + 42790232 42790232 42790232 CAGCCTGGAGTGCAGTGGTACAATTGTAGCTCACTGCAGCCTGGACCTCCTGGGATCAAGGGATT CAGCCTGGAGTGCAGTGGTACAATTGTAGCTCGCTGCAGCCTGGACCTCCTGGGATCAAGGGATT A G BICRAL Ensembl:ENSG00000112624 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs949885095 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 19814 RMVar_ID_19814 Human_SNP_ID_274784808 A-to-I Human chr6 + 42790298 42790298 42790298 CCCCAACCTCAGCCTCCCAAGTAGCTGGGACTATAGAAATGCAACACCATGCCCAGATAATTTAA CCCCAACCTCAGCCTCCCAAGTAGCTGGGACTGTAGAAATGCAACACCATGCCCAGATAATTTAA A G BICRAL Ensembl:ENSG00000112624 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs954890678 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15829571 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 19815 RMVar_ID_19815 Human_SNP_ID_274787606 A-to-I Human chr6 + 42801145 42801145 42801145 GTTGTGGCAGGTGCCTGTAATCCCAGCTACTCAGGAGGCTAAAACAGGGGAATTGCTAGAACCTG GTTGTGGCAGGTGCCTGTAATCCCAGCTACTCCGGAGGCTAAAACAGGGGAATTGCTAGAACCTG A C BICRAL Ensembl:ENSG00000112624 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1405747510 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 19816 RMVar_ID_19816 Human_SNP_ID_274797767 A-to-I Human chr6 + 42843857 42843857 42843857 GAGTCTCACTCTGTCACCCAGGCGAGTGCAATAGCACGATCTCGGCTCACTGCAACCTCCTTCTC GAGTCTCACTCTGTCACCCAGGCGAGTGCAATGGCACGATCTCGGCTCACTGCAACCTCCTTCTC A G BICRAL Ensembl:ENSG00000112624 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs796718974 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 19817 RMVar_ID_19817 Human_SNP_ID_274797768 A-to-I Human chr6 + 42843857 42843857 42843857 GAGTCTCACTCTGTCACCCAGGCGAGTGCAATAGCACGATCTCGGCTCACTGCAACCTCCTTCTC GAGTCTCACTCTGTCACCCAGGCGAGTGCAATTGCACGATCTCGGCTCACTGCAACCTCCTTCTC A T BICRAL Ensembl:ENSG00000112624 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs796718974 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 19818 RMVar_ID_19818 Human_SNP_ID_274800681 A-to-I Human chr6 + 42854423 42854423 42854423 TCACACCTGTCTCAAACTCCTGGGCCCAAGCCATCCACCCACCTCAGCCTCCCAAAGTACCTGGA TCACACCTGTCTCAAACTCCTGGGCCCAAGCCGTCCACCCACCTCAGCCTCCCAAAGTACCTGGA A G BICRAL Ensembl:ENSG00000112624 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs950325478 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267047,RMVar_hsa_circ_332559,RMVar_hsa_circ_44225,RMVar_hsa_circ_265805,RMVar_hsa_circ_238488,RMVar_hsa_circ_310798,RMVar_hsa_circ_361470,RMVar_hsa_circ_329266,RMVar_hsa_circ_47749,RMVar_hsa_circ_289680,RMVar_hsa_circ_238489,RMVar_hsa_circ_15335 19819 RMVar_ID_19819 Human_SNP_ID_274807771 A-to-I Human chr6 + 42881634 42881634 42881634 TCACTCTTGCCTAGAGTGGAGTGCAGTGGCACAATCTCGACTCACTGCAACCTCTGCCTACTGGG TCACTCTTGCCTAGAGTGGAGTGCAGTGGCACCATCTCGACTCACTGCAACCTCTGCCTACTGGG A C RPL7L1 Ensembl:ENSG00000146223 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1412515829 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17576342 RMVar_hsa_circ_61877,RMVar_hsa_circ_317713,RMVar_hsa_circ_118388,RMVar_hsa_circ_238491 19820 RMVar_ID_19820 Human_SNP_ID_274807772 A-to-I Human chr6 + 42881634 42881634 42881634 TCACTCTTGCCTAGAGTGGAGTGCAGTGGCACAATCTCGACTCACTGCAACCTCTGCCTACTGGG TCACTCTTGCCTAGAGTGGAGTGCAGTGGCACGATCTCGACTCACTGCAACCTCTGCCTACTGGG A G RPL7L1 Ensembl:ENSG00000146223 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1412515829 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17576342 RMVar_hsa_circ_61877,RMVar_hsa_circ_317713,RMVar_hsa_circ_118388,RMVar_hsa_circ_238491 19821 RMVar_ID_19821 Human_SNP_ID_274807786 A-to-I Human chr6 + 42881688 42881688 42881688 TGCCTACTGGGCTCAAGCAATTCTCGTGCCTCAGCCAACCAAGTAGCTAGGATTACAAGCATGCG TGCCTACTGGGCTCAAGCAATTCTCGTGCCTCGGCCAACCAAGTAGCTAGGATTACAAGCATGCG A G RPL7L1 Ensembl:ENSG00000146223 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1363486118 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7607855 RMVar_hsa_circ_61877,RMVar_hsa_circ_317713,RMVar_hsa_circ_118388,RMVar_hsa_circ_238491 19822 RMVar_ID_19822 Human_SNP_ID_274807840 A-to-I Human chr6 + 42881926 42881926 42881926 GGGATTACAAGGATGTGCCACCATGCCCTGCTAATTTTTGTATTTTTAGTAGAGACCGGGTTTCA GGGATTACAAGGATGTGCCACCATGCCCTGCTTATTTTTGTATTTTTAGTAGAGACCGGGTTTCA A T RPL7L1 Ensembl:ENSG00000146223 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1396804357 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61877,RMVar_hsa_circ_317713,RMVar_hsa_circ_118388,RMVar_hsa_circ_238491 19823 RMVar_ID_19823 Human_SNP_ID_274807855 A-to-I Human chr6 + 42882022 42882022 42882022 GACTCAAGTGATCTGCCCACCTCGGCCTCCCAAAGTGCTGCGATTACTGATGTCAGCCACCCCAC GACTCAAGTGATCTGCCCACCTCGGCCTCCCAGAGTGCTGCGATTACTGATGTCAGCCACCCCAC A G RPL7L1 Ensembl:ENSG00000146223 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1241753070 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61877,RMVar_hsa_circ_317713,RMVar_hsa_circ_118388,RMVar_hsa_circ_238491 19824 RMVar_ID_19824 Human_SNP_ID_274808098 A-to-I Human chr6 + 42882861 42882861 42882861 TCAGGTGGCAGAGGTTGCAGTGAGCCGAGATCATATCACTGCACTCCAGCCTGGGCGACAGAGCG TCAGGTGGCAGAGGTTGCAGTGAGCCGAGATCGTATCACTGCACTCCAGCCTGGGCGACAGAGCG A G RPL7L1 Ensembl:ENSG00000146223 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs902268072 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10285743,Human_RBP_ID_26047690 RMVar_hsa_circ_61877,RMVar_hsa_circ_317713,RMVar_hsa_circ_118388,RMVar_hsa_circ_238491 19825 RMVar_ID_19825 Human_SNP_ID_274808127 A-to-I Human chr6 + 42882951 42882951 42882951 AACAAGGAGTGAGGTCTTGTGTTACCCAGGCTAGAGTGCAGTGGCAGGATCATAGCTCATTGCAG AACAAGGAGTGAGGTCTTGTGTTACCCAGGCTGGAGTGCAGTGGCAGGATCATAGCTCATTGCAG A G RPL7L1 Ensembl:ENSG00000146223 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-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 19826 RMVar_ID_19826 Human_SNP_ID_274809234 A-to-I Human chr6 + 42886847 42886847 42886847 GAAACCCTGTCTCTACTAAAAATACAAAAATGAGCTGGGTGTGGTGGCGCGTGCCTGTAGTCCCA GAAACCCTGTCTCTACTAAAAATACAAAAATGGGCTGGGTGTGGTGGCGCGTGCCTGTAGTCCCA A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs528472688 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22618473 RMVar_hsa_circ_118388,RMVar_hsa_circ_238491 19827 RMVar_ID_19827 Human_SNP_ID_274809246 A-to-I Human chr6 + 42886873 42886873 42886873 AAAATGAGCTGGGTGTGGTGGCGCGTGCCTGTAGTCCCAGCTACTCGAGAGGCTAAGGCAGGAAA AAAATGAGCTGGGTGTGGTGGCGCGTGCCTGTGGTCCCAGCTACTCGAGAGGCTAAGGCAGGAAA A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1138999 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22618474 Human_miRNA_ID_277276,Human_miRNA_ID_2790799 RMVar_hsa_circ_118388,RMVar_hsa_circ_238491 19828 RMVar_ID_19828 Human_SNP_ID_274809263 A-to-I Human chr6 + 42886943 42886943 42886943 TTGAACCCAGGAGGCAGAGATTGCAGTGAGCCAAGATTGCACCAGTGCACTCCAGCTGGGCGACA TTGAACCCAGGAGGCAGAGATTGCAGTGAGCCGAGATTGCACCAGTGCACTCCAGCTGGGCGACA A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1139003 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_664694,Human_RBP_ID_2021485,Human_RBP_ID_4890148,Human_RBP_ID_9194708,Human_RBP_ID_18865995,Human_RBP_ID_23062211,Human_RBP_ID_23314746,Human_RBP_ID_26047695,Human_RBP_ID_26536801,Human_RBP_ID_27524818 RMVar_hsa_circ_118388,RMVar_hsa_circ_238491 19829 RMVar_ID_19829 Human_SNP_ID_274809266 A-to-I Human chr6 + 42886954 42886954 42886954 AGGCAGAGATTGCAGTGAGCCAAGATTGCACCAGTGCACTCCAGCTGGGCGACAGAGCGAGACTC AGGCAGAGATTGCAGTGAGCCAAGATTGCACCGGTGCACTCCAGCTGGGCGACAGAGCGAGACTC A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1000375280 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_664694,Human_RBP_ID_2021485,Human_RBP_ID_4890148,Human_RBP_ID_7607895,Human_RBP_ID_9194708,Human_RBP_ID_15829802,Human_RBP_ID_18865995,Human_RBP_ID_23062211,Human_RBP_ID_23314746,Human_RBP_ID_26047695,Human_RBP_ID_26536801 RMVar_hsa_circ_118388,RMVar_hsa_circ_238491 19830 RMVar_ID_19830 Human_SNP_ID_274809615 A-to-I Human chr6 + 42888198 42888198 42888198 TTTCTCTTTGAGACAGTCTCACCCTGTTGCCCAGGCTGGAGCGCAGTGGCATGATCTCAGCTCAT TTTCTCTTTGAGACAGTCTCACCCTGTTGCCCGGGCTGGAGCGCAGTGGCATGATCTCAGCTCAT A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1481625375 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252300,Human_RBP_ID_664709,Human_RBP_ID_24163580,Human_RBP_ID_26536816 Human_miRNA_ID_1159590 19831 RMVar_ID_19831 Human_SNP_ID_274809623 A-to-I Human chr6 + 42888216 42888216 42888216 TCACCCTGTTGCCCAGGCTGGAGCGCAGTGGCATGATCTCAGCTCATTGCAGCCTCCACCTCCTG TCACCCTGTTGCCCAGGCTGGAGCGCAGTGGCGTGATCTCAGCTCATTGCAGCCTCCACCTCCTG A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs878875910 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252300,Human_RBP_ID_664709 19832 RMVar_ID_19832 Human_SNP_ID_274809625 A-to-I Human chr6 + 42888224 42888224 42888224 TTGCCCAGGCTGGAGCGCAGTGGCATGATCTCAGCTCATTGCAGCCTCCACCTCCTGGGTTCAAG TTGCCCAGGCTGGAGCGCAGTGGCATGATCTCGGCTCATTGCAGCCTCCACCTCCTGGGTTCAAG A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs11558567 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252300,Human_RBP_ID_27347399 19833 RMVar_ID_19833 Human_SNP_ID_274809628 A-to-I Human chr6 + 42888234 42888234 42888234 TGGAGCGCAGTGGCATGATCTCAGCTCATTGCAGCCTCCACCTCCTGGGTTCAAGTGATTCTGCC TGGAGCGCAGTGGCATGATCTCAGCTCATTGCGGCCTCCACCTCCTGGGTTCAAGTGATTCTGCC A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1167593296 Functional Loss SNV dbSNP153 33..33 33 - - - 19834 RMVar_ID_19834 Human_SNP_ID_274809629 A-to-I Human chr6 + 42888241 42888238 42888241 CAGTGGCATGATCTCAGCTCATTGCAGCCTCCACCTCCTGGGTTCAAGTGATTCTGCCTCAGCCC CAGTGGCATGATCTCAGCTCATTGCAGCCT___CCTCCTGGGTTCAAGTGATTCTGCCTCAGCCC TCCA T RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1455916663 Functional Loss DEL dbSNP153 31..33 33 - - - 19835 RMVar_ID_19835 Human_SNP_ID_274809631 A-to-I Human chr6 + 42888241 42888241 42888241 CAGTGGCATGATCTCAGCTCATTGCAGCCTCCACCTCCTGGGTTCAAGTGATTCTGCCTCAGCCC CAGTGGCATGATCTCAGCTCATTGCAGCCTCCGCCTCCTGGGTTCAAGTGATTCTGCCTCAGCCC A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs3209050 Functional Loss SNV dbSNP153 33..33 33 - - - 19836 RMVar_ID_19836 Human_SNP_ID_274809637 A-to-I Human chr6 + 42888269 42888269 42888269 CTCCACCTCCTGGGTTCAAGTGATTCTGCCTCAGCCCCTTGATCAGCTGGGATTACATGCATGTA CTCCACCTCCTGGGTTCAAGTGATTCTGCCTCGGCCCCTTGATCAGCTGGGATTACATGCATGTA A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1253502313 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26536819 19837 RMVar_ID_19837 Human_SNP_ID_274809642 A-to-I Human chr6 + 42888291 42888291 42888291 ATTCTGCCTCAGCCCCTTGATCAGCTGGGATTACATGCATGTACCACCACACCCAGCTAATTCTT ATTCTGCCTCAGCCCCTTGATCAGCTGGGATTGCATGCATGTACCACCACACCCAGCTAATTCTT A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1318315394 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4890182 19838 RMVar_ID_19838 Human_SNP_ID_274809649 A-to-I Human chr6 + 42888309 42888309 42888309 GATCAGCTGGGATTACATGCATGTACCACCACACCCAGCTAATTCTTGTATTTTTAGTAGAGATG GATCAGCTGGGATTACATGCATGTACCACCACGCCCAGCTAATTCTTGTATTTTTAGTAGAGATG A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs1289789723 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_756891 19839 RMVar_ID_19839 Human_SNP_ID_274809650 A-to-I Human chr6 + 42888313 42888313 42888313 AGCTGGGATTACATGCATGTACCACCACACCCAGCTAATTCTTGTATTTTTAGTAGAGATGGAGA AGCTGGGATTACATGCATGTACCACCACACCCGGCTAATTCTTGTATTTTTAGTAGAGATGGAGA A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs1455587741 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_756891,Human_miRNA_ID_1360430 19840 RMVar_ID_19840 Human_SNP_ID_274809651 A-to-I Human chr6 + 42888317 42888317 42888317 GGGATTACATGCATGTACCACCACACCCAGCTAATTCTTGTATTTTTAGTAGAGATGGAGACAGA GGGATTACATGCATGTACCACCACACCCAGCTGATTCTTGTATTTTTAGTAGAGATGGAGACAGA A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1376086272 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24163581 Human_miRNA_ID_756891 19841 RMVar_ID_19841 Human_SNP_ID_274809660 A-to-I Human chr6 + 42888349 42888349 42888349 AATTCTTGTATTTTTAGTAGAGATGGAGACAGAGTTTCACCATGTAGGCCAGGCTAGTCTCAAAC AATTCTTGTATTTTTAGTAGAGATGGAGACAGTGTTTCACCATGTAGGCCAGGCTAGTCTCAAAC A T RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1486654285 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_664710,Human_RBP_ID_7607911,Human_RBP_ID_15829828,Human_RBP_ID_18371458,Human_RBP_ID_26539498 19842 RMVar_ID_19842 Human_SNP_ID_274809663 A-to-I Human chr6 + 42888362 42888362 42888362 TTAGTAGAGATGGAGACAGAGTTTCACCATGTAGGCCAGGCTAGTCTCAAACTCCTGACCTCAAG TTAGTAGAGATGGAGACAGAGTTTCACCATGTGGGCCAGGCTAGTCTCAAACTCCTGACCTCAAG A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1348051650 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26536821 19843 RMVar_ID_19843 Human_SNP_ID_274809664 A-to-I Human chr6 + 42888367 42888367 42888367 AGAGATGGAGACAGAGTTTCACCATGTAGGCCAGGCTAGTCTCAAACTCCTGACCTCAAGTGATC AGAGATGGAGACAGAGTTTCACCATGTAGGCCGGGCTAGTCTCAAACTCCTGACCTCAAGTGATC A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1304984453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26536821 19844 RMVar_ID_19844 Human_SNP_ID_274809665 A-to-I Human chr6 + 42888372 42888372 42888372 TGGAGACAGAGTTTCACCATGTAGGCCAGGCTAGTCTCAAACTCCTGACCTCAAGTGATCCACAA TGGAGACAGAGTTTCACCATGTAGGCCAGGCTGGTCTCAAACTCCTGACCTCAAGTGATCCACAA A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1226897826 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26536821 19845 RMVar_ID_19845 Human_SNP_ID_274809667 A-to-I Human chr6 + 42888378 42888378 42888378 CAGAGTTTCACCATGTAGGCCAGGCTAGTCTCAAACTCCTGACCTCAAGTGATCCACAAGCCTGG CAGAGTTTCACCATGTAGGCCAGGCTAGTCTCGAACTCCTGACCTCAAGTGATCCACAAGCCTGG A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1326338583 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26007651,Human_RBP_ID_26536821 19846 RMVar_ID_19846 Human_SNP_ID_274809668 A-to-I Human chr6 + 42888379 42888379 42888379 AGAGTTTCACCATGTAGGCCAGGCTAGTCTCAAACTCCTGACCTCAAGTGATCCACAAGCCTGGG AGAGTTTCACCATGTAGGCCAGGCTAGTCTCAGACTCCTGACCTCAAGTGATCCACAAGCCTGGG A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569236566 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26536821 19847 RMVar_ID_19847 Human_SNP_ID_274809677 A-to-I Human chr6 + 42888432 42888432 42888432 CACAAGCCTGGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCAACTGCGCCCAGCTCTTGTGT CACAAGCCTGGGCCTCCCAAAGTGCTGGGATTGCAGGCATGAGCAACTGCGCCCAGCTCTTGTGT A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1193669983 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_791029,Human_RBP_ID_4890187,Human_RBP_ID_23195639 19848 RMVar_ID_19848 Human_SNP_ID_274809680 A-to-I Human chr6 + 42888438 42888438 42888438 CCTGGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCAACTGCGCCCAGCTCTTGTGTACCTTA CCTGGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCAACTGCGCCCAGCTCTTGTGTACCTTA A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1209792927 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23195639,Human_RBP_ID_26540164 19849 RMVar_ID_19849 Human_SNP_ID_274809735 A-to-I Human chr6 + 42888592 42888592 42888592 CAAGATAGATTTTTCCCTTCATAGTGGCAGATAGTGTTAACCCCTGCACCATCTGTAACTCAGAA CAAGATAGATTTTTCCCTTCATAGTGGCAGATGGTGTTAACCCCTGCACCATCTGTAACTCAGAA A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-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 19850 RMVar_ID_19850 Human_SNP_ID_274809851 A-to-I Human chr6 + 42889167 42889167 42889167 ACTGCCTTAAAACATGCCAGCTTAGGCTGGGCACGGTGGCTCACACCTGTAATCTCAACACTTCA ACTGCCTTAAAACATGCCAGCTTAGGCTGGGCGCGGTGGCTCACACCTGTAATCTCAACACTTCA A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs11558575 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_664720,Human_RBP_ID_18076789,Human_RBP_ID_26540169 19851 RMVar_ID_19851 Human_SNP_ID_274809855 A-to-I Human chr6 + 42889179 42889179 42889179 CATGCCAGCTTAGGCTGGGCACGGTGGCTCACACCTGTAATCTCAACACTTCAGGAGGCTGAGGC CATGCCAGCTTAGGCTGGGCACGGTGGCTCACGCCTGTAATCTCAACACTTCAGGAGGCTGAGGC A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1055972 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18084883,Human_RBP_ID_26536833 19852 RMVar_ID_19852 Human_SNP_ID_274809856 A-to-I Human chr6 + 42889185 42889185 42889185 AGCTTAGGCTGGGCACGGTGGCTCACACCTGTAATCTCAACACTTCAGGAGGCTGAGGCAGGCAG AGCTTAGGCTGGGCACGGTGGCTCACACCTGTGATCTCAACACTTCAGGAGGCTGAGGCAGGCAG A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-Seq:(High) rs1562515264 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18084883,Human_RBP_ID_26536833 19853 RMVar_ID_19853 Human_SNP_ID_274809860 A-to-I Human chr6 + 42889199 42889199 42889199 ACGGTGGCTCACACCTGTAATCTCAACACTTCAGGAGGCTGAGGCAGGCAGATCACTTGAGGTCA ACGGTGGCTCACACCTGTAATCTCAACACTTCGGGAGGCTGAGGCAGGCAGATCACTTGAGGTCA A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1259710292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26829667 19854 RMVar_ID_19854 Human_SNP_ID_274809861 A-to-I Human chr6 + 42889221 42889221 42889221 TCAACACTTCAGGAGGCTGAGGCAGGCAGATCACTTGAGGTCAGGAGTTCGAGACCAGCCTGACC TCAACACTTCAGGAGGCTGAGGCAGGCAGATCGCTTGAGGTCAGGAGTTCGAGACCAGCCTGACC A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215898569 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26829667 Human_miRNA_ID_198594,Human_miRNA_ID_699276,Human_miRNA_ID_704199,Human_miRNA_ID_1288411 19855 RMVar_ID_19855 Human_SNP_ID_274809865 A-to-I Human chr6 + 42889240 42889240 42889240 AGGCAGGCAGATCACTTGAGGTCAGGAGTTCGAGACCAGCCTGACCAACATGGAGAAATTCTGTC AGGCAGGCAGATCACTTGAGGTCAGGAGTTCGGGACCAGCCTGACCAACATGGAGAAATTCTGTC A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1372301513 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15829858 19856 RMVar_ID_19856 Human_SNP_ID_274809866 A-to-I Human chr6 + 42889245 42889245 42889245 GGCAGATCACTTGAGGTCAGGAGTTCGAGACCAGCCTGACCAACATGGAGAAATTCTGTCCCTAC GGCAGATCACTTGAGGTCAGGAGTTCGAGACCGGCCTGACCAACATGGAGAAATTCTGTCCCTAC A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1134325 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15829858 19857 RMVar_ID_19857 Human_SNP_ID_274809869 A-to-I Human chr6 + 42889254 42889254 42889254 CTTGAGGTCAGGAGTTCGAGACCAGCCTGACCAACATGGAGAAATTCTGTCCCTACTGAAAATAC CTTGAGGTCAGGAGTTCGAGACCAGCCTGACCGACATGGAGAAATTCTGTCCCTACTGAAAATAC A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1562515320 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_246862,Human_miRNA_ID_249397 19858 RMVar_ID_19858 Human_SNP_ID_274809878 A-to-I Human chr6 + 42889285 42889285 42889285 CAACATGGAGAAATTCTGTCCCTACTGAAAATACAAAATTAGCCGGATGTGGTGGTGCATGCCTG CAACATGGAGAAATTCTGTCCCTACTGAAAATGCAAAATTAGCCGGATGTGGTGGTGCATGCCTG A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1134326 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26540170 19859 RMVar_ID_19859 Human_SNP_ID_274809879 A-to-I Human chr6 + 42889288 42889288 42889288 CATGGAGAAATTCTGTCCCTACTGAAAATACAAAATTAGCCGGATGTGGTGGTGCATGCCTGTAA CATGGAGAAATTCTGTCCCTACTGAAAATACAGAATTAGCCGGATGTGGTGGTGCATGCCTGTAA A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1260757271 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26540170 19860 RMVar_ID_19860 Human_SNP_ID_274809880 A-to-I Human chr6 + 42889293 42889293 42889293 AGAAATTCTGTCCCTACTGAAAATACAAAATTAGCCGGATGTGGTGGTGCATGCCTGTAATCCCA AGAAATTCTGTCCCTACTGAAAATACAAAATTCGCCGGATGTGGTGGTGCATGCCTGTAATCCCA A C RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1134327 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26540170 19861 RMVar_ID_19861 Human_SNP_ID_274809881 A-to-I Human chr6 + 42889293 42889293 42889293 AGAAATTCTGTCCCTACTGAAAATACAAAATTAGCCGGATGTGGTGGTGCATGCCTGTAATCCCA AGAAATTCTGTCCCTACTGAAAATACAAAATTGGCCGGATGTGGTGGTGCATGCCTGTAATCCCA A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1134327 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26540170 19862 RMVar_ID_19862 Human_SNP_ID_274809884 A-to-I Human chr6 + 42889299 42889299 42889299 TCTGTCCCTACTGAAAATACAAAATTAGCCGGATGTGGTGGTGCATGCCTGTAATCCCAGCTACT TCTGTCCCTACTGAAAATACAAAATTAGCCGGTTGTGGTGGTGCATGCCTGTAATCCCAGCTACT A T RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1349241861 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26539503 19863 RMVar_ID_19863 Human_SNP_ID_274809903 A-to-I Human chr6 + 42889373 42889373 42889373 GAGGCAAGAGAATTGCTTGAACCCAGGGAGGCAGAGGTTGCAGTGAGCCGAGATCACACCATTGC GAGGCAAGAGAATTGCTTGAACCCAGGGAGGCGGAGGTTGCAGTGAGCCGAGATCACACCATTGC A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1134330 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_172115,Human_RBP_ID_23314747,Human_RBP_ID_26540171,Human_RBP_ID_27524829 19864 RMVar_ID_19864 Human_SNP_ID_274809906 A-to-I Human chr6 + 42889398 42889398 42889398 GGGAGGCAGAGGTTGCAGTGAGCCGAGATCACACCATTGCACTCCACCTTGGGCAACAAAAGCAA GGGAGGCAGAGGTTGCAGTGAGCCGAGATCACGCCATTGCACTCCACCTTGGGCAACAAAAGCAA A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-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 19865 RMVar_ID_19865 Human_SNP_ID_274822578 A-to-I Human chr6 + 42936557 42936556 42936558 AAGGTTTTTGTGTGTTTGTTTGTTTTGGAGACAGAGTCTCACACTCTGTTGCCCAAGCTGGAGCG AAGGTTTTTGTGTGTTTGTTTGTTTTGGAGAC__AGTCTCACACTCTGTTGCCCAAGCTGGAGCG CAG C CNPY3 Ensembl:ENSG00000137161 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs202139019 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_42101,RMVar_hsa_circ_238495,RMVar_hsa_circ_310109,RMVar_hsa_circ_238496,RMVar_hsa_circ_91585 19866 RMVar_ID_19866 Human_SNP_ID_274822633 A-to-I Human chr6 + 42936770 42936770 42936770 TGCTGGCCAGGGGGTCTCGAACTCCTGACCTCAGGTGATCAGCCCACCTTGGCCTCTCAAAGTGC TGCTGGCCAGGGGGTCTCGAACTCCTGACCTCGGGTGATCAGCCCACCTTGGCCTCTCAAAGTGC A G CNPY3 Ensembl:ENSG00000137161 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1021113128 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42101,RMVar_hsa_circ_238495,RMVar_hsa_circ_310109,RMVar_hsa_circ_238496,RMVar_hsa_circ_91585 19867 RMVar_ID_19867 Human_SNP_ID_274823601 A-to-I Human chr6 + 42940411 42940411 42940411 TGTAGTAGAGACGGGGTTTCACCATCTTGGCCAGGATAGTTTTGAACTCCTGACCTCATGATCCA TGTAGTAGAGACGGGGTTTCACCATCTTGGCCGGGATAGTTTTGAACTCCTGACCTCATGATCCA A G AL035587.1 Ensembl:ENSG00000231113 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971086836 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15829993 19868 RMVar_ID_19868 Human_SNP_ID_274823608 A-to-I Human chr6 + 42940436 42940436 42940436 CTTGGCCAGGATAGTTTTGAACTCCTGACCTCATGATCCATCTGCCTCGGCTTCCCAAAGTGTTG CTTGGCCAGGATAGTTTTGAACTCCTGACCTCGTGATCCATCTGCCTCGGCTTCCCAAAGTGTTG A G AL035587.1 Ensembl:ENSG00000231113 lincRNA exon GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1561803446 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5251030,Human_RBP_ID_15829993 19869 RMVar_ID_19869 Human_SNP_ID_274823617 A-to-I Human chr6 + 42940461 42940461 42940461 TGACCTCATGATCCATCTGCCTCGGCTTCCCAAAGTGTTGGGATTACAGGTGGGAGCCACTGCGC TGACCTCATGATCCATCTGCCTCGGCTTCCCAGAGTGTTGGGATTACAGGTGGGAGCCACTGCGC A G AL035587.1 Ensembl:ENSG00000231113 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1175898706 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5251030 19870 RMVar_ID_19870 Human_SNP_ID_274823894 A-to-I Human chr6 + 42941524 42941524 42941524 CTTTCTTTTTTGGAACAGGATCTCCCTTTGTCACCCAGGCTGGAGTGCAGTGGCGTGATCATGAC CTTTCTTTTTTGGAACAGGATCTCCCTTTGTCGCCCAGGCTGGAGTGCAGTGGCGTGATCATGAC A G AL035587.1 Ensembl:ENSG00000231113 lincRNA exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1354272824 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3822944,Human_RBP_ID_7656087,Human_RBP_ID_26539511 Human_Splice_Rec_770632,Human_Splice_Rec_770633 19871 RMVar_ID_19871 Human_SNP_ID_274823911 A-to-I Human chr6 + 42941602 42941602 42941602 CAACCTCTCAGGCTCAAGTGATCCTCCTGAATAGTTGGGACCATAGGTATGCACCACTGTACCTG CAACCTCTCAGGCTCAAGTGATCCTCCTGAATGGTTGGGACCATAGGTATGCACCACTGTACCTG A G AL035587.1 Ensembl:ENSG00000231113 lincRNA exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs918739923 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7607991,Human_RBP_ID_15830031 Human_Splice_Rec_770632,Human_Splice_Rec_770633 19872 RMVar_ID_19872 Human_SNP_ID_274823981 A-to-I Human chr6 + 42941842 42941842 42941842 TATTTGTTTGCAAGAGTCTCACTCTGTCACCCAGGCTGGAGTGCACTGGCACAATCTTGTCTCAC TATTTGTTTGCAAGAGTCTCACTCTGTCACCCGGGCTGGAGTGCACTGGCACAATCTTGTCTCAC A G AL035587.1 Ensembl:ENSG00000231113 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973160598 Functional Loss SNV dbSNP153 33..33 33 - - - 19873 RMVar_ID_19873 Human_SNP_ID_274824016 A-to-I Human chr6 + 42941999 42941999 42941999 TTTTGTATTTTTAATAGAGACGGGGTTTCACCATGATGGCCAGGCTGGTCTCGAACTCCTCACCT TTTTGTATTTTTAATAGAGACGGGGTTTCACCGTGATGGCCAGGCTGGTCTCGAACTCCTCACCT A G AL035587.1 Ensembl:ENSG00000231113 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs921612157 Functional Loss SNV dbSNP153 33..33 33 - - - 19874 RMVar_ID_19874 Human_SNP_ID_274824067 A-to-I Human chr6 + 42942191 42942190 42942191 GGGAGGCTGAGGCAGGACAATTGCTTGAAACCAAGAGGCGGAGGTTGCAGTGAGCCGAGATTGCA GGGAGGCTGAGGCAGGACAATTGCTTGAAACC_AGAGGCGGAGGTTGCAGTGAGCCGAGATTGCA CA C AL035587.1 Ensembl:ENSG00000231113 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1315940725 Functional Loss DEL dbSNP153 33..33 33 - - - 19875 RMVar_ID_19875 Human_SNP_ID_274824123 A-to-I Human chr6 + 42942331 42942331 42942331 CAGGGTCTCCACATGTTGGCCAGGCTGGTCTCAAACTCCTGGACTCAAGCAATCCTCCCATCTCG CAGGGTCTCCACATGTTGGCCAGGCTGGTCTCGAACTCCTGGACTCAAGCAATCCTCCCATCTCG A G AL035587.1 Ensembl:ENSG00000231113 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs895864027 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_664765 19876 RMVar_ID_19876 Human_SNP_ID_274824133 A-to-I Human chr6 + 42942372 42942372 42942372 GACTCAAGCAATCCTCCCATCTCGGCCTCCCAAAGTGCTGGGATTACACGTGTGAGCCACCATGC GACTCAAGCAATCCTCCCATCTCGGCCTCCCAGAGTGCTGGGATTACACGTGTGAGCCACCATGC A G AL035587.1 Ensembl:ENSG00000231113 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1241309143 Functional Loss SNV dbSNP153 33..33 33 - - - 19877 RMVar_ID_19877 Human_SNP_ID_274824340 A-to-I Human chr6 + 42943089 42943089 42943089 GAAATTAATCTACCTGATATACAGAAATTCATATAGATGAATTTCTACCTGTTCTGAATCAAAAC GAAATTAATCTACCTGATATACAGAAATTCATGTAGATGAATTTCTACCTGTTCTGAATCAAAAC A G AL035587.1 Ensembl:ENSG00000231113 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs960388078 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17307270,Human_RBP_ID_26536853,Human_RBP_ID_27524857 19878 RMVar_ID_19878 Human_SNP_ID_274824345 A-to-I Human chr6 + 42943103 42943103 42943103 TGATATACAGAAATTCATATAGATGAATTTCTACCTGTTCTGAATCAAAACACAAGCCATGTGCA TGATATACAGAAATTCATATAGATGAATTTCTGCCTGTTCTGAATCAAAACACAAGCCATGTGCA A G AL035587.1 Ensembl:ENSG00000231113 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1230524749 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17307270,Human_RBP_ID_18371477,Human_RBP_ID_26536854 19879 RMVar_ID_19879 Human_SNP_ID_274824359 A-to-I Human chr6 + 42943183 42943183 42943183 CCCAGCTACTTGGGAGGTGGCTTGAGAGGATCACTTGAGCCCAGGAGTTCCAGTCCAGCCTGAGC CCCAGCTACTTGGGAGGTGGCTTGAGAGGATCGCTTGAGCCCAGGAGTTCCAGTCCAGCCTGAGC A G AL035587.1 Ensembl:ENSG00000231113 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs950666195 Functional Loss SNV dbSNP153 33..33 33 - - - 19880 RMVar_ID_19880 Human_SNP_ID_274824371 A-to-I Human chr6 + 42943239 42943238 42943240 AGCCTGAGCAACACAGTGAGACCCTCATCTCTAAAAAGCGAATAAAAACAAAAAAAACACCAAAA AGCCTGAGCAACACAGTGAGACCCTCATCTCT__AAAGCGAATAAAAACAAAAAAAACACCAAAA TAA T AL035587.1 Ensembl:ENSG00000231113 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs921363774 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_1395607 19881 RMVar_ID_19881 Human_SNP_ID_274824529 A-to-I Human chr6 + 42943952 42943952 42943952 GACCAGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGCCCGAGGTGGGTGGATCACG GACCAGGCACGGTGGCTCACGCCTGTAATCCCGGCACTTTGGGAGCCCGAGGTGGGTGGATCACG A G AL035587.1 Ensembl:ENSG00000231113 lincRNA exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs181266235 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_770635 Human_miRNA_ID_3146507,Human_miRNA_ID_3146742,Human_miRNA_ID_3154805,Human_miRNA_ID_3156678,Human_miRNA_ID_3161477,Human_miRNA_ID_3161712,Human_miRNA_ID_3168037,Human_miRNA_ID_3168255,Human_miRNA_ID_3168475,Human_miRNA_ID_3168694,Human_miRNA_ID_3168914,Human_miRNA_ID_3180308,Human_miRNA_ID_3180527,Human_miRNA_ID_3183954,Human_miRNA_ID_3195377,Human_miRNA_ID_3197775,Human_miRNA_ID_3198156,Human_miRNA_ID_3198539,Human_miRNA_ID_3198756,Human_miRNA_ID_3199027,Human_miRNA_ID_3199395,Human_miRNA_ID_3199723,Human_miRNA_ID_3199959,Human_miRNA_ID_3200879,Human_miRNA_ID_3215809 RMVar_hsa_circ_238499 19882 RMVar_ID_19882 Human_SNP_ID_274828385 A-to-I Human chr6 + 42958957 42958957 42958957 TTTAGTAGAGACAGGGTTTTAGCATCTTGGCCAGGCTGATCTTGAACTCCTGACCACGTGATCCA TTTAGTAGAGACAGGGTTTTAGCATCTTGGCCGGGCTGATCTTGAACTCCTGACCACGTGATCCA A G RF00017-4567 RNACentral:URS000093B3AD SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs892503087 Functional Loss SNV dbSNP153 33..33 33 - - - 19883 RMVar_ID_19883 Human_SNP_ID_274833940 A-to-I Human chr6 - 42977735 42977735 42977735 AGATGGGGTCTTGCTCTGTCACCCAGGCTGGAATGTGGTGATGCGATCTCGGCTTACTGCAACCT AGATGGGGTCTTGCTCTGTCACCCAGGCTGGAGTGTGGTGATGCGATCTCGGCTTACTGCAACCT T C PEX6 Ensembl:ENSG00000124587 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1397921918 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102668,RMVar_hsa_circ_98476,RMVar_hsa_circ_238514,RMVar_hsa_circ_238516 19884 RMVar_ID_19884 Human_SNP_ID_274839107 A-to-I Human chr6 + 42997030 42997029 42997031 TCTTTGTTTTTTTATGTATTTATTTTTGAGACAGACTCTTCCTTTGTTGCCCAGGCTGGAGTGTC TCTTTGTTTTTTTATGTATTTATTTTTGAGAC__ACTCTTCCTTTGTTGCCCAGGCTGGAGTGTC CAG C PPP2R5D Ensembl:ENSG00000112640 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1362090721 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_7608099,Human_RBP_ID_15830391,Human_RBP_ID_18866047 RMVar_hsa_circ_110308,RMVar_hsa_circ_238517 19885 RMVar_ID_19885 Human_SNP_ID_274839706 A-to-I Human chr6 - 42998680 42998680 42998680 TTGCCCAGGCTGGTCTCAAACTCTGGAGCTCAAGCAATCCACCCGCCTCAGCCTCCCAAAGTGCT TTGCCCAGGCTGGTCTCAAACTCTGGAGCTCATGCAATCCACCCGCCTCAGCCTCCCAAAGTGCT T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924270458 Functional Loss SNV dbSNP153 33..33 33 - - - 19886 RMVar_ID_19886 Human_SNP_ID_274839707 A-to-I Human chr6 - 42998680 42998680 42998680 TTGCCCAGGCTGGTCTCAAACTCTGGAGCTCAAGCAATCCACCCGCCTCAGCCTCCCAAAGTGCT TTGCCCAGGCTGGTCTCAAACTCTGGAGCTCACGCAATCCACCCGCCTCAGCCTCCCAAAGTGCT T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924270458 Functional Loss SNV dbSNP153 33..33 33 - - - 19887 RMVar_ID_19887 Human_SNP_ID_274844349 A-to-I Human chr6 + 43016030 43016030 43016030 TGATCTCGGCTCACTCCAACCTCCGCCACCCGAGTGCAAGCAATTCTCCTGCCTCAGCCTCCTGA TGATCTCGGCTCACTCCAACCTCCGCCACCCGCGTGCAAGCAATTCTCCTGCCTCAGCCTCCTGA A C KLHDC3 Ensembl:ENSG00000124702 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042655147 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8645520 19888 RMVar_ID_19888 Human_SNP_ID_274844351 A-to-I Human chr6 + 43016039 43016039 43016039 CTCACTCCAACCTCCGCCACCCGAGTGCAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGG CTCACTCCAACCTCCGCCACCCGAGTGCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGG A G KLHDC3 Ensembl:ENSG00000124702 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1297268837 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8645520 19889 RMVar_ID_19889 Human_SNP_ID_274844389 A-to-I Human chr6 + 43016207 43016207 43016207 CACCTGCCTCGGCCTCTCAGGGTGCTGGGATTACAGGTGTGAGCCACTGTGCCCAGCCCCTTCCC CACCTGCCTCGGCCTCTCAGGGTGCTGGGATTCCAGGTGTGAGCCACTGTGCCCAGCCCCTTCCC A C KLHDC3 Ensembl:ENSG00000124702 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1316542878 Functional Loss SNV dbSNP153 33..33 33 - - - 19890 RMVar_ID_19890 Human_SNP_ID_274848580 A-to-I Human chr6 + 43029700 43029700 43029700 CAGGCTAGAGTACAGTGGTGCAATCTCGCCTCACTGCAACCTCCACCTCCCAGGTTCAAGTGATT CAGGCTAGAGTACAGTGGTGCAATCTCGCCTCGCTGCAACCTCCACCTCCCAGGTTCAAGTGATT A G RRP36 Ensembl:ENSG00000124541 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs925544755 Functional Loss SNV dbSNP153 33..33 33 - - - 19891 RMVar_ID_19891 Human_SNP_ID_274848584 A-to-I Human chr6 + 43029725 43029724 43029725 TCGCCTCACTGCAACCTCCACCTCCCAGGTTCAAGTGATTCTTGTGCCTCAGCCTCCCGAGTAGC TCGCCTCACTGCAACCTCCACCTCCCAGGTTC_AGTGATTCTTGTGCCTCAGCCTCCCGAGTAGC CA C RRP36 Ensembl:ENSG00000124541 Protein coding intron GSE100210;GSE107867;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,30559470,31158229,31158229,31158229 RNA-Seq:(High) rs1407675842 Functional Loss DEL dbSNP153 33..33 33 - - - 19892 RMVar_ID_19892 Human_SNP_ID_274848585 A-to-I Human chr6 + 43029730 43029730 43029730 TCACTGCAACCTCCACCTCCCAGGTTCAAGTGATTCTTGTGCCTCAGCCTCCCGAGTAGCTGACA TCACTGCAACCTCCACCTCCCAGGTTCAAGTGGTTCTTGTGCCTCAGCCTCCCGAGTAGCTGACA A G RRP36 Ensembl:ENSG00000124541 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910879572 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26007916,Human_RBP_ID_26540191 19893 RMVar_ID_19893 Human_SNP_ID_274848603 A-to-I Human chr6 + 43029800 43029798 43029801 CACCAAGCCCAGCTAATTTCTTTCGTATTTTTAGTAGAGATAGAGTTTTGCCATGTTGGCTAGTT CACCAAGCCCAGCTAATTTCTTTCGTATTTT___TAGAGATAGAGTTTTGCCATGTTGGCTAGTT TTAG T RRP36 Ensembl:ENSG00000124541 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1385563263 Functional Loss DEL dbSNP153 32..34 33 - - - 19894 RMVar_ID_19894 Human_SNP_ID_274848604 A-to-I Human chr6 + 43029807 43029801 43029807 CCCAGCTAATTTCTTTCGTATTTTTAGTAGAGATAGAGTTTTGCCATGTTGGCTAGTTTGATCTT CCCAGCTAATTTCTTTCGTATTTTTAG______TAGAGTTTTGCCATGTTGGCTAGTTTGATCTT GTAGAGA G RRP36 Ensembl:ENSG00000124541 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1307664390 Functional Loss DEL dbSNP153 28..33 33 - - - 19895 RMVar_ID_19895 Human_SNP_ID_274848609 A-to-I Human chr6 + 43029809 43029809 43029809 CAGCTAATTTCTTTCGTATTTTTAGTAGAGATAGAGTTTTGCCATGTTGGCTAGTTTGATCTTAA CAGCTAATTTCTTTCGTATTTTTAGTAGAGATGGAGTTTTGCCATGTTGGCTAGTTTGATCTTAA A G RRP36 Ensembl:ENSG00000124541 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs887769570 Functional Loss SNV dbSNP153 33..33 33 - - - 19896 RMVar_ID_19896 Human_SNP_ID_274848619 A-to-I Human chr6 + 43029872 43029872 43029872 AAACTCTTGGCCTCAAGTGATCTGCCTGCCTCAGACTCCCAAAGTGCTGGGATTACAGGCGTTGA AAACTCTTGGCCTCAAGTGATCTGCCTGCCTCGGACTCCCAAAGTGCTGGGATTACAGGCGTTGA A G RRP36 Ensembl:ENSG00000124541 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1182984492 Functional Loss SNV dbSNP153 33..33 33 - - - 19897 RMVar_ID_19897 Human_SNP_ID_274848623 A-to-I Human chr6 + 43029880 43029880 43029880 GGCCTCAAGTGATCTGCCTGCCTCAGACTCCCAAAGTGCTGGGATTACAGGCGTTGAGCCACCGT GGCCTCAAGTGATCTGCCTGCCTCAGACTCCCGAAGTGCTGGGATTACAGGCGTTGAGCCACCGT A G RRP36 Ensembl:ENSG00000124541 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1015576011 Functional Loss SNV dbSNP153 33..33 33 - - - 19898 RMVar_ID_19898 Human_SNP_ID_274848624 A-to-I Human chr6 + 43029881 43029881 43029881 GCCTCAAGTGATCTGCCTGCCTCAGACTCCCAAAGTGCTGGGATTACAGGCGTTGAGCCACCGTT GCCTCAAGTGATCTGCCTGCCTCAGACTCCCAGAGTGCTGGGATTACAGGCGTTGAGCCACCGTT A G RRP36 Ensembl:ENSG00000124541 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1233460977 Functional Loss SNV dbSNP153 33..33 33 - - - 19899 RMVar_ID_19899 Human_SNP_ID_274848734 A-to-I Human chr6 + 43030363 43030363 43030363 GAGGCAGGCGGATCACCTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCCCAT GAGGCAGGCGGATCACCTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCCAT A G RRP36 Ensembl:ENSG00000124541 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1411747574 Functional Loss SNV dbSNP153 33..33 33 - - - 19900 RMVar_ID_19900 Human_SNP_ID_274848773 A-to-I Human chr6 + 43030521 43030521 43030521 GGGAGGTAGAGGTTGCAGTGAGCCAAGATCGCACCACTGCACTCCAGCCTGGGCAAAAAGAGTGA GGGAGGTAGAGGTTGCAGTGAGCCAAGATCGCGCCACTGCACTCCAGCCTGGGCAAAAAGAGTGA A G RRP36 Ensembl:ENSG00000124541 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251968306 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27524907 19901 RMVar_ID_19901 Human_SNP_ID_274848937 A-to-I Human chr6 + 43030757 43030757 43030757 GGGTGTGGTGGTGGGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAAGCAGGAGAATTGCTTGAA GGGTGTGGTGGTGGGCGCCTGTAATCCCAGCTGCTCAGGAGGCTGAAGCAGGAGAATTGCTTGAA A G RRP36 Ensembl:ENSG00000124541 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1414671635 Functional Loss SNV dbSNP153 33..33 33 - - - 19902 RMVar_ID_19902 Human_SNP_ID_274848938 A-to-I Human chr6 + 43030761 43030761 43030761 GTGGTGGTGGGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAAGCAGGAGAATTGCTTGAACGCG GTGGTGGTGGGCGCCTGTAATCCCAGCTACTCCGGAGGCTGAAGCAGGAGAATTGCTTGAACGCG A C RRP36 Ensembl:ENSG00000124541 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1000046847 Functional Loss SNV dbSNP153 33..33 33 - - - 19903 RMVar_ID_19903 Human_SNP_ID_274848939 A-to-I Human chr6 + 43030761 43030761 43030761 GTGGTGGTGGGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAAGCAGGAGAATTGCTTGAACGCG GTGGTGGTGGGCGCCTGTAATCCCAGCTACTCTGGAGGCTGAAGCAGGAGAATTGCTTGAACGCG A T RRP36 Ensembl:ENSG00000124541 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1000046847 Functional Loss SNV dbSNP153 33..33 33 - - - 19904 RMVar_ID_19904 Human_SNP_ID_274848960 A-to-I Human chr6 + 43030817 43030817 43030817 TTGAACGCGGGAGGCGGAGGTTGCAGTGAACCAAGATCGCGCCACTGCACTCCAGCCTGGGCGAC TTGAACGCGGGAGGCGGAGGTTGCAGTGAACCGAGATCGCGCCACTGCACTCCAGCCTGGGCGAC A G RRP36 Ensembl:ENSG00000124541 Protein coding intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs34961677 Functional Loss SNV dbSNP153 33..33 33 - - - 19905 RMVar_ID_19905 Human_SNP_ID_274849090 A-to-I Human chr6 + 43031291 43031291 43031291 AGCCAGGCGTGGTGGCGGGTGCCTGTAGTCCCAGCTACTCTGGAGGCTGAGGCAGGAGGATGGCA AGCCAGGCGTGGTGGCGGGTGCCTGTAGTCCCGGCTACTCTGGAGGCTGAGGCAGGAGGATGGCA A G RRP36 Ensembl:ENSG00000124541 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1349858980 Functional Loss SNV dbSNP153 33..33 33 - - - 19906 RMVar_ID_19906 Human_SNP_ID_274849091 A-to-I Human chr6 + 43031295 43031295 43031295 AGGCGTGGTGGCGGGTGCCTGTAGTCCCAGCTACTCTGGAGGCTGAGGCAGGAGGATGGCATGAA AGGCGTGGTGGCGGGTGCCTGTAGTCCCAGCTGCTCTGGAGGCTGAGGCAGGAGGATGGCATGAA A G RRP36 Ensembl:ENSG00000124541 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1237808284 Functional Loss SNV dbSNP153 33..33 33 - - - 19907 RMVar_ID_19907 Human_SNP_ID_274849229 A-to-I Human chr6 + 43031673 43031673 43031673 GGGAGGCTGAGGCAGGAGAATTGCTTGAACCTAGGAGGCGGAGGTTGCGGTGAGCCAAGATTGCG GGGAGGCTGAGGCAGGAGAATTGCTTGAACCTGGGAGGCGGAGGTTGCGGTGAGCCAAGATTGCG A G RRP36 Ensembl:ENSG00000124541 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1183967666 Functional Loss SNV dbSNP153 33..33 33 - - - 19908 RMVar_ID_19908 Human_SNP_ID_274849544 A-to-I Human chr6 + 43032824 43032824 43032824 AAAGAAAGAATGCCTACCTTAAAAGCAGCTCTATGCCCCCAGTTAGGAGACTGAGGTGGGACAAT AAAGAAAGAATGCCTACCTTAAAAGCAGCTCTGTGCCCCCAGTTAGGAGACTGAGGTGGGACAAT A G RRP36 Ensembl:ENSG00000124541 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs966124499 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7608294,Human_RBP_ID_26540201 19909 RMVar_ID_19909 Human_SNP_ID_274852340 A-to-I Human chr6 - 43042544 43042544 43042544 CTGAGGGCAGGAGTTTGAGGCCAGCCTGGCCAACATGGCCAAACCCCATCTCTACTAAAAATACA CTGAGGGCAGGAGTTTGAGGCCAGCCTGGCCAGCATGGCCAAACCCCATCTCTACTAAAAATACA T C CUL7 Ensembl:ENSG00000044090 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs979907801 Functional Loss SNV dbSNP153 33..33 33 - - - 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 19910 RMVar_ID_19910 Human_SNP_ID_274859053 A-to-I Human chr6 + 43064403 43064403 43064403 AAAATTAGCCTGATGTGGTCGTGTGCACCTATAGCCTCAGCTACTCTGGAGGCTGAGGTGGGAGG AAAATTAGCCTGATGTGGTCGTGTGCACCTATGGCCTCAGCTACTCTGGAGGCTGAGGTGGGAGG A G KLC4 Ensembl:ENSG00000137171 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474288756 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5986 19911 RMVar_ID_19911 Human_SNP_ID_274859849 A-to-I Human chr6 + 43067489 43067489 43067489 GTAGTTGTATTGAGTACAACTTTGTTAAAAGAAATAGCAAAGTGGCCTGGGCACAGTGGCTCACG GTAGTTGTATTGAGTACAACTTTGTTAAAAGACATAGCAAAGTGGCCTGGGCACAGTGGCTCACG A C KLC4 Ensembl:ENSG00000137171 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs971491476 Functional Loss SNV dbSNP153 33..33 33 - - - 19912 RMVar_ID_19912 Human_SNP_ID_274860501 A-to-I Human chr6 + 43069370 43069370 43069370 AGGCTCAAGTGATCCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGTACGTGCTACCACG AGGCTCAAGTGATCCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGTACGTGCTACCACG A G KLC4 Ensembl:ENSG00000137171 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1041125333 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26008047 19913 RMVar_ID_19913 Human_SNP_ID_274877351 A-to-I Human chr6 + 43134222 43134222 43134222 CACCACACCTGGCTAATTTTTGTATTTTTAGTAGAGGCGATGTTTTACCATGTTGGCCAGGCTAG CACCACACCTGGCTAATTTTTGTATTTTTAGTTGAGGCGATGTTTTACCATGTTGGCCAGGCTAG A T PTK7 Ensembl:ENSG00000112655 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1185968927 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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 19914 RMVar_ID_19914 Human_SNP_ID_274877362 A-to-I Human chr6 + 43134248 43134248 43134248 TTTAGTAGAGGCGATGTTTTACCATGTTGGCCAGGCTAGTCTCAAACTCTTGACCTCAAGTGATC TTTAGTAGAGGCGATGTTTTACCATGTTGGCCGGGCTAGTCTCAAACTCTTGACCTCAAGTGATC A G PTK7 Ensembl:ENSG00000112655 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1316465639 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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 19915 RMVar_ID_19915 Human_SNP_ID_274882480 A-to-I Human chr6 + 43152879 43152879 43152879 AGGACCTCGGCTCACTGTAGCCTCCGCCTCCCAGGTTCAAATGATTCTCCTGCCTCGGCCCCCTG AGGACCTCGGCTCACTGTAGCCTCCGCCTCCCGGGTTCAAATGATTCTCCTGCCTCGGCCCCCTG A G PTK7 Ensembl:ENSG00000112655 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474848441 Functional Loss SNV dbSNP153 33..33 33 - - - 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_238571 19916 RMVar_ID_19916 Human_SNP_ID_274894642 A-to-I Human chr6 + 43197126 43197126 43197126 TAGAGTGCAGTGGCACGATCTCGACTCACTGTAACCTCTGCTTCCTGGGTTCAAGCAATTCTCAT TAGAGTGCAGTGGCACGATCTCGACTCACTGTCACCTCTGCTTCCTGGGTTCAAGCAATTCTCAT A C CUL9 Ensembl:ENSG00000112659 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270122590 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105711,RMVar_hsa_circ_238581,RMVar_hsa_circ_121603,RMVar_hsa_circ_238582,RMVar_hsa_circ_101701,RMVar_hsa_circ_238583 19917 RMVar_ID_19917 Human_SNP_ID_274900049 A-to-I Human chr6 - 43219094 43219094 43219094 GCCTCAATCTCCTGGACTCAAGCAATCCTCCCACCTCAACCTCCTGAGTAGGCAGGACTATAGGT GCCTCAATCTCCTGGACTCAAGCAATCCTCCCGCCTCAACCTCCTGAGTAGGCAGGACTATAGGT T C AL133375.1 Ensembl:ENSG00000245261 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903505633 Functional Loss SNV dbSNP153 33..33 33 - - - 19918 RMVar_ID_19918 Human_SNP_ID_274926517 A-to-I Human chr6 - 43320810 43320810 43320810 TCACTGCATCCTTGAGCTCCTGGACTCAAGCAATCCTCCCACTTCAGCCTCCAAGTAACTGGGAC TCACTGCATCCTTGAGCTCCTGGACTCAAGCAGTCCTCCCACTTCAGCCTCCAAGTAACTGGGAC T C ZNF318 Ensembl:ENSG00000171467 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1398166633 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40769,RMVar_hsa_circ_66844 19919 RMVar_ID_19919 Human_SNP_ID_274934613 A-to-I Human chr6 - 43351890 43351890 43351890 GTGATCCACCCGCCTTAGCCTCCCAAAGTGCTAGGATTACAGGCGTGAGCTCCCACACCCTGCCA GTGATCCACCCGCCTTAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCTCCCACACCCTGCCA T C ZNF318 Ensembl:ENSG00000171467 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1360912839 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107122,RMVar_hsa_circ_54792,RMVar_hsa_circ_123851,RMVar_hsa_circ_238609,RMVar_hsa_circ_238610,RMVar_hsa_circ_268133,RMVar_hsa_circ_307947,RMVar_hsa_circ_238612 19920 RMVar_ID_19920 Human_SNP_ID_274937654 A-to-I Human chr6 - 43362414 43362414 43362414 AGAGTCTTGCACTGTTGCCTGGCTGGAGTGCAATGCTGCAATCTCGGCTCACTGCAACCTCCGCC AGAGTCTTGCACTGTTGCCTGGCTGGAGTGCAGTGCTGCAATCTCGGCTCACTGCAACCTCCGCC T C ZNF318 Ensembl:ENSG00000171467 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1035828461 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107122,RMVar_hsa_circ_238609,RMVar_hsa_circ_48731 19921 RMVar_ID_19921 Human_SNP_ID_274937772 A-to-I Human chr6 - 43362783 43362783 43362783 TGTAGATGTTTGGGCCTGGCGCAGTGGCTCATACCTGTAATCCCAGCACTTTGGGAGGCTGAGGT TGTAGATGTTTGGGCCTGGCGCAGTGGCTCATTCCTGTAATCCCAGCACTTTGGGAGGCTGAGGT T A ZNF318 Ensembl:ENSG00000171467 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs752633449 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107122,RMVar_hsa_circ_238609,RMVar_hsa_circ_48731 19922 RMVar_ID_19922 Human_SNP_ID_274937773 A-to-I Human chr6 - 43362783 43362783 43362783 TGTAGATGTTTGGGCCTGGCGCAGTGGCTCATACCTGTAATCCCAGCACTTTGGGAGGCTGAGGT TGTAGATGTTTGGGCCTGGCGCAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGT T C ZNF318 Ensembl:ENSG00000171467 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs752633449 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107122,RMVar_hsa_circ_238609,RMVar_hsa_circ_48731 19923 RMVar_ID_19923 Human_SNP_ID_274962908 A-to-I Human chr6 + 43458493 43458493 43458493 GTGGTCCACCGGCCTTGGCCTCCCAAAGTGCTAGGGTTACAGGCATGAGTCACCGTGCCCAGCCT GTGGTCCACCGGCCTTGGCCTCCCAAAGTGCTGGGGTTACAGGCATGAGTCACCGTGCCCAGCCT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1336547204 Functional Loss SNV dbSNP153 33..33 33 - - - 19924 RMVar_ID_19924 Human_SNP_ID_274969465 A-to-I Human chr6 + 43484996 43484996 43484996 GTGATCCACCCACCTGGGCCTCCCAAAGTGCCAGGATTACAGGCGTGAGCCACCACGCCCAGCCT GTGATCCACCCACCTGGGCCTCCCAAAGTGCCGGGATTACAGGCGTGAGCCACCACGCCCAGCCT A G TJAP1 Ensembl:ENSG00000137221 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1253966243 Functional Loss SNV dbSNP153 33..33 33 - - - 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_44288,RMVar_hsa_circ_346758,RMVar_hsa_circ_49694 19925 RMVar_ID_19925 Human_SNP_ID_274977899 A-to-I Human chr6 - 43514159 43514159 43514159 TCGGTTCACTGCAACCTCCGCTTCCCGGGTTCAGGCAATTCTCCTGCCTCAGCCTCCTGAGTAGC TCGGTTCACTGCAACCTCCGCTTCCCGGGTTCGGGCAATTCTCCTGCCTCAGCCTCCTGAGTAGC T C YIPF3 Ensembl:ENSG00000137207 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1303205110 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_238636,RMVar_hsa_circ_62927 19926 RMVar_ID_19926 Human_SNP_ID_274978164 A-to-I Human chr6 - 43515110 43515110 43515110 CCCGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCATGAACCTGGGAGGCGGAGGCG CCCGTAGTCCCAGCTACTCGGGAGGCTGAGGCCGGAGAATGGCATGAACCTGGGAGGCGGAGGCG T G YIPF3 Ensembl:ENSG00000137207 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1344986134 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_238636,RMVar_hsa_circ_62927 19927 RMVar_ID_19927 Human_SNP_ID_274984359 A-to-I Human chr6 + 43535037 43535037 43535037 CCCAAAGGCCAGGCGCAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGTGG CCCAAAGGCCAGGCGCAGTGGCTCATGCCTGTCATCCCAGCACTTTGGGAGGCTGAGGTGGGTGG A C POLR1C Ensembl:ENSG00000171453 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1035922972 Functional Loss SNV dbSNP153 33..33 33 - - - 19928 RMVar_ID_19928 Human_SNP_ID_274985069 A-to-I Human chr6 + 43537232 43537232 43537232 GGCCCCAAGAGATCCTCCTGCCCTGGCCTCCCAAAGTGCTGAAATTATAGGCATGAGCCACTATT GGCCCCAAGAGATCCTCCTGCCCTGGCCTCCCGAAGTGCTGAAATTATAGGCATGAGCCACTATT A G POLR1C Ensembl:ENSG00000171453 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924056708 Functional Loss SNV dbSNP153 33..33 33 - - - 19929 RMVar_ID_19929 Human_SNP_ID_274985225 A-to-I Human chr6 - 43537919 43537919 43537919 GGATTACAGGTGTGCGCCACCACGCCTGGCTAATTTTTTGTATTTTTAGTAGATACAGGGTTTTG GGATTACAGGTGTGCGCCACCACGCCTGGCTAGTTTTTTGTATTTTTAGTAGATACAGGGTTTTG T C XPO5 Ensembl:ENSG00000124571 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1384662456 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27844,RMVar_hsa_circ_33944,RMVar_hsa_circ_62820,RMVar_hsa_circ_367386,RMVar_hsa_circ_306097,RMVar_hsa_circ_301510,RMVar_hsa_circ_17210,RMVar_hsa_circ_29776,RMVar_hsa_circ_238649,RMVar_hsa_circ_265595,RMVar_hsa_circ_278176,RMVar_hsa_circ_312930,RMVar_hsa_circ_326066,RMVar_hsa_circ_360754,RMVar_hsa_circ_287024,RMVar_hsa_circ_276160,RMVar_hsa_circ_238651,RMVar_hsa_circ_93095,RMVar_hsa_circ_238650,RMVar_hsa_circ_238648 19930 RMVar_ID_19930 Human_SNP_ID_274985422 A-to-I Human chr6 + 43538360 43538360 43538360 TTTAGTAGAGATGGGGTTTTGTCATGTTGGCCAGGTTGGTCTCAAACTCTTAGCCTCAAGGATCC TTTAGTAGAGATGGGGTTTTGTCATGTTGGCCTGGTTGGTCTCAAACTCTTAGCCTCAAGGATCC A T POLR1C Ensembl:ENSG00000171453 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879060422 Functional Loss SNV dbSNP153 33..33 33 - - - 19931 RMVar_ID_19931 Human_SNP_ID_274985424 A-to-I Human chr6 + 43538385 43538385 43538385 GTTGGCCAGGTTGGTCTCAAACTCTTAGCCTCAAGGATCCGCCTGCCTCGGCCTCCCAAACTGCT GTTGGCCAGGTTGGTCTCAAACTCTTAGCCTCGAGGATCCGCCTGCCTCGGCCTCCCAAACTGCT A G POLR1C Ensembl:ENSG00000171453 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs972304454 Functional Loss SNV dbSNP153 33..33 33 - - - 19932 RMVar_ID_19932 Human_SNP_ID_274986845 A-to-I Human chr6 - 43543910 43543910 43543910 CACTGTGAGAGGCCAAGGCGCATGGATCACTTAAGGTCAACAGTTCGAGACTAGCCCAATAAACA CACTGTGAGAGGCCAAGGCGCATGGATCACTTGAGGTCAACAGTTCGAGACTAGCCCAATAAACA T C XPO5 Ensembl:ENSG00000124571 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1467338698 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15833375 RMVar_hsa_circ_27844,RMVar_hsa_circ_33944,RMVar_hsa_circ_62820,RMVar_hsa_circ_367386,RMVar_hsa_circ_306097,RMVar_hsa_circ_301510,RMVar_hsa_circ_17210,RMVar_hsa_circ_29776,RMVar_hsa_circ_238649,RMVar_hsa_circ_265595,RMVar_hsa_circ_278176,RMVar_hsa_circ_312930,RMVar_hsa_circ_326066,RMVar_hsa_circ_360754,RMVar_hsa_circ_287024,RMVar_hsa_circ_276160,RMVar_hsa_circ_238651,RMVar_hsa_circ_93095,RMVar_hsa_circ_238650,RMVar_hsa_circ_238648 19933 RMVar_ID_19933 Human_SNP_ID_274987040 A-to-I Human chr6 - 43544675 43544669 43544676 CAGCTGAGCCTGCTTCAGTCTCCCAAAGTGCTAGCATTACAAGTGTGAACCACCACACCCAGCCC CAGCTGAGCCTGCTTCAGTCTCCCAAAGTGC_______ACAAGTGTGAACCACCACACCCAGCCC TAATGCTA T XPO5 Ensembl:ENSG00000124571 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1011339956 Functional Loss DEL dbSNP153 32..38 33 - - - Human_RBP_ID_15833423 RMVar_hsa_circ_27844,RMVar_hsa_circ_33944,RMVar_hsa_circ_62820,RMVar_hsa_circ_367386,RMVar_hsa_circ_306097,RMVar_hsa_circ_301510,RMVar_hsa_circ_17210,RMVar_hsa_circ_29776,RMVar_hsa_circ_238649,RMVar_hsa_circ_265595,RMVar_hsa_circ_278176,RMVar_hsa_circ_312930,RMVar_hsa_circ_326066,RMVar_hsa_circ_360754,RMVar_hsa_circ_287024,RMVar_hsa_circ_276160,RMVar_hsa_circ_238651,RMVar_hsa_circ_93095,RMVar_hsa_circ_238650,RMVar_hsa_circ_238648 19934 RMVar_ID_19934 Human_SNP_ID_274987256 A-to-I Human chr6 - 43545660 43545660 43545660 TTTGTCACCCAGGCTGGGAGTGCAGTGGTGCAATCTTGGCTCACTGCAACCTCCGCCTCCCAGGC TTTGTCACCCAGGCTGGGAGTGCAGTGGTGCAGTCTTGGCTCACTGCAACCTCCGCCTCCCAGGC T C XPO5 Ensembl:ENSG00000124571 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1275949781 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27844,RMVar_hsa_circ_33944,RMVar_hsa_circ_62820,RMVar_hsa_circ_367386,RMVar_hsa_circ_306097,RMVar_hsa_circ_301510,RMVar_hsa_circ_17210,RMVar_hsa_circ_29776,RMVar_hsa_circ_238649,RMVar_hsa_circ_265595,RMVar_hsa_circ_278176,RMVar_hsa_circ_312930,RMVar_hsa_circ_326066,RMVar_hsa_circ_360754,RMVar_hsa_circ_287024,RMVar_hsa_circ_276160,RMVar_hsa_circ_238651,RMVar_hsa_circ_93095,RMVar_hsa_circ_238650,RMVar_hsa_circ_238648 19935 RMVar_ID_19935 Human_SNP_ID_274988563 A-to-I Human chr6 - 43551180 43551180 43551180 TGCTACATTGCCCAGGCTGGACTCAAATTACTAGTCTCAAGGGATCCTCACACCTCACCCTTCTG TGCTACATTGCCCAGGCTGGACTCAAATTACTGGTCTCAAGGGATCCTCACACCTCACCCTTCTG T C XPO5 Ensembl:ENSG00000124571 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1007274374 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_949675,Human_RBP_ID_1069610,Human_RBP_ID_5400913,Human_RBP_ID_19129422,Human_RBP_ID_22682924 RMVar_hsa_circ_27844,RMVar_hsa_circ_33944,RMVar_hsa_circ_367386,RMVar_hsa_circ_306097,RMVar_hsa_circ_301510,RMVar_hsa_circ_17210,RMVar_hsa_circ_29776,RMVar_hsa_circ_238649,RMVar_hsa_circ_278176,RMVar_hsa_circ_312930,RMVar_hsa_circ_360754,RMVar_hsa_circ_276160,RMVar_hsa_circ_238651,RMVar_hsa_circ_93095,RMVar_hsa_circ_238650,RMVar_hsa_circ_293279,RMVar_hsa_circ_337990,RMVar_hsa_circ_341244,RMVar_hsa_circ_368128,RMVar_hsa_circ_340680,RMVar_hsa_circ_308342,RMVar_hsa_circ_312694,RMVar_hsa_circ_298260,RMVar_hsa_circ_121992,RMVar_hsa_circ_39225,RMVar_hsa_circ_100801,RMVar_hsa_circ_238653,RMVar_hsa_circ_238655,RMVar_hsa_circ_238657,RMVar_hsa_circ_238656,RMVar_hsa_circ_238654,RMVar_hsa_circ_238652,RMVar_hsa_circ_266908,RMVar_hsa_circ_97485,RMVar_hsa_circ_108545,RMVar_hsa_circ_238659,RMVar_hsa_circ_238663,RMVar_hsa_circ_4252,RMVar_hsa_circ_112763,RMVar_hsa_circ_318557,RMVar_hsa_circ_238661,RMVar_hsa_circ_238662,RMVar_hsa_circ_344502,RMVar_hsa_circ_277065,RMVar_hsa_circ_302178,RMVar_hsa_circ_122838,RMVar_hsa_circ_98374,RMVar_hsa_circ_10477,RMVar_hsa_circ_238667,RMVar_hsa_circ_238669,RMVar_hsa_circ_238670,RMVar_hsa_circ_238668,RMVar_hsa_circ_238665,RMVar_hsa_circ_238666,RMVar_hsa_circ_238664 19936 RMVar_ID_19936 Human_SNP_ID_274990904 A-to-I Human chr6 - 43559876 43559876 43559876 GGGAAGTTGAAGCTGCATTGAGCTGAGATCGCAGCACTGCACTCCAGCCTAGGCAATGAGAGTGA GGGAAGTTGAAGCTGCATTGAGCTGAGATCGCCGCACTGCACTCCAGCCTAGGCAATGAGAGTGA T G XPO5 Ensembl:ENSG00000124571 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1466490683 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15833720 RMVar_hsa_circ_33944,RMVar_hsa_circ_301510,RMVar_hsa_circ_17210,RMVar_hsa_circ_29776,RMVar_hsa_circ_360754,RMVar_hsa_circ_238651,RMVar_hsa_circ_93095,RMVar_hsa_circ_293279,RMVar_hsa_circ_341244,RMVar_hsa_circ_368128,RMVar_hsa_circ_340680,RMVar_hsa_circ_121992,RMVar_hsa_circ_39225,RMVar_hsa_circ_20530,RMVar_hsa_circ_100801,RMVar_hsa_circ_238653,RMVar_hsa_circ_238652,RMVar_hsa_circ_97485,RMVar_hsa_circ_238659,RMVar_hsa_circ_238663,RMVar_hsa_circ_4252,RMVar_hsa_circ_112763,RMVar_hsa_circ_238662,RMVar_hsa_circ_277065,RMVar_hsa_circ_122838,RMVar_hsa_circ_10477,RMVar_hsa_circ_238665,RMVar_hsa_circ_238666,RMVar_hsa_circ_238664,RMVar_hsa_circ_120293,RMVar_hsa_circ_238676,RMVar_hsa_circ_319836,RMVar_hsa_circ_115386,RMVar_hsa_circ_238675,RMVar_hsa_circ_330300,RMVar_hsa_circ_374100,RMVar_hsa_circ_72653,RMVar_hsa_circ_238677,RMVar_hsa_circ_238679,RMVar_hsa_circ_238678,RMVar_hsa_circ_280262,RMVar_hsa_circ_311043,RMVar_hsa_circ_359745,RMVar_hsa_circ_117528,RMVar_hsa_circ_67555,RMVar_hsa_circ_238683,RMVar_hsa_circ_238684,RMVar_hsa_circ_238682,RMVar_hsa_circ_107077,RMVar_hsa_circ_293115,RMVar_hsa_circ_35753,RMVar_hsa_circ_238685,RMVar_hsa_circ_238686 19937 RMVar_ID_19937 Human_SNP_ID_274990955 A-to-I Human chr6 - 43560094 43560094 43560094 GACTTTGAGGCTGGGTGCGGTGGCTCACGCCTATAATCCCAGCTCTATGGAAGGCTGAGGCGGGA GACTTTGAGGCTGGGTGCGGTGGCTCACGCCTGTAATCCCAGCTCTATGGAAGGCTGAGGCGGGA T C XPO5 Ensembl:ENSG00000124571 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1394738145 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8645795 RMVar_hsa_circ_33944,RMVar_hsa_circ_301510,RMVar_hsa_circ_17210,RMVar_hsa_circ_29776,RMVar_hsa_circ_360754,RMVar_hsa_circ_238651,RMVar_hsa_circ_93095,RMVar_hsa_circ_293279,RMVar_hsa_circ_341244,RMVar_hsa_circ_368128,RMVar_hsa_circ_340680,RMVar_hsa_circ_121992,RMVar_hsa_circ_39225,RMVar_hsa_circ_20530,RMVar_hsa_circ_100801,RMVar_hsa_circ_238653,RMVar_hsa_circ_238652,RMVar_hsa_circ_97485,RMVar_hsa_circ_238659,RMVar_hsa_circ_238663,RMVar_hsa_circ_4252,RMVar_hsa_circ_112763,RMVar_hsa_circ_238662,RMVar_hsa_circ_277065,RMVar_hsa_circ_122838,RMVar_hsa_circ_10477,RMVar_hsa_circ_238665,RMVar_hsa_circ_238666,RMVar_hsa_circ_238664,RMVar_hsa_circ_120293,RMVar_hsa_circ_238676,RMVar_hsa_circ_319836,RMVar_hsa_circ_115386,RMVar_hsa_circ_238675,RMVar_hsa_circ_330300,RMVar_hsa_circ_374100,RMVar_hsa_circ_72653,RMVar_hsa_circ_238677,RMVar_hsa_circ_238679,RMVar_hsa_circ_238678,RMVar_hsa_circ_280262,RMVar_hsa_circ_311043,RMVar_hsa_circ_359745,RMVar_hsa_circ_117528,RMVar_hsa_circ_67555,RMVar_hsa_circ_238683,RMVar_hsa_circ_238684,RMVar_hsa_circ_238682,RMVar_hsa_circ_107077,RMVar_hsa_circ_293115,RMVar_hsa_circ_35753,RMVar_hsa_circ_238685,RMVar_hsa_circ_238686 19938 RMVar_ID_19938 Human_SNP_ID_274992250 A-to-I Human chr6 - 43564983 43564983 43564983 GGGAGGCAGAGGTTGCTGTGAGCTGAGATCACACCACTCTACTCCAGACTGGGCAACAAAGTGAG GGGAGGCAGAGGTTGCTGTGAGCTGAGATCACGCCACTCTACTCCAGACTGGGCAACAAAGTGAG T C XPO5 Ensembl:ENSG00000124571 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs112255077 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19133805 Clinvar_Rec_70,Clinvar_Rec_71,Clinvar_Rec_72,Clinvar_Rec_73,Clinvar_Rec_74,Clinvar_Rec_75,Clinvar_Rec_76 RMVar_hsa_circ_33944,RMVar_hsa_circ_301510,RMVar_hsa_circ_17210,RMVar_hsa_circ_29776,RMVar_hsa_circ_360754,RMVar_hsa_circ_238651,RMVar_hsa_circ_93095,RMVar_hsa_circ_293279,RMVar_hsa_circ_341244,RMVar_hsa_circ_368128,RMVar_hsa_circ_121992,RMVar_hsa_circ_20530,RMVar_hsa_circ_100801,RMVar_hsa_circ_238653,RMVar_hsa_circ_238652,RMVar_hsa_circ_238659,RMVar_hsa_circ_238663,RMVar_hsa_circ_4252,RMVar_hsa_circ_277065,RMVar_hsa_circ_122838,RMVar_hsa_circ_10477,RMVar_hsa_circ_238665,RMVar_hsa_circ_238664,RMVar_hsa_circ_120293,RMVar_hsa_circ_238676,RMVar_hsa_circ_115386,RMVar_hsa_circ_330300,RMVar_hsa_circ_72653,RMVar_hsa_circ_238677,RMVar_hsa_circ_238678,RMVar_hsa_circ_280262,RMVar_hsa_circ_311043,RMVar_hsa_circ_359745,RMVar_hsa_circ_117528,RMVar_hsa_circ_238683,RMVar_hsa_circ_238684,RMVar_hsa_circ_238682,RMVar_hsa_circ_107077,RMVar_hsa_circ_37507,RMVar_hsa_circ_277648,RMVar_hsa_circ_238685,RMVar_hsa_circ_238686,RMVar_hsa_circ_309193,RMVar_hsa_circ_370970,RMVar_hsa_circ_102607,RMVar_hsa_circ_124840,RMVar_hsa_circ_238688,RMVar_hsa_circ_238690,RMVar_hsa_circ_238691,RMVar_hsa_circ_238689,RMVar_hsa_circ_93836,RMVar_hsa_circ_238687,RMVar_hsa_circ_373135,RMVar_hsa_circ_73728,RMVar_hsa_circ_238697,RMVar_hsa_circ_238694,RMVar_hsa_circ_238695,RMVar_hsa_circ_279218,RMVar_hsa_circ_349969,RMVar_hsa_circ_361379,RMVar_hsa_circ_67436,RMVar_hsa_circ_238696 19939 RMVar_ID_19939 Human_SNP_ID_274994257 A-to-I Human chr6 - 43571680 43571680 43571680 CCTTAGCCTCCCAAGTAGCTGGGATTATAGGCATGTGGTACCATGCCCAGCTAATTTTGTTTTTG CCTTAGCCTCCCAAGTAGCTGGGATTATAGGCGTGTGGTACCATGCCCAGCTAATTTTGTTTTTG T C XPO5 Ensembl:ENSG00000124571 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1397954109 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17210,RMVar_hsa_circ_360754,RMVar_hsa_circ_293279,RMVar_hsa_circ_368128,RMVar_hsa_circ_121992,RMVar_hsa_circ_20530,RMVar_hsa_circ_238652,RMVar_hsa_circ_238663,RMVar_hsa_circ_10477,RMVar_hsa_circ_72653,RMVar_hsa_circ_311043,RMVar_hsa_circ_238684,RMVar_hsa_circ_37507,RMVar_hsa_circ_238686,RMVar_hsa_circ_309193,RMVar_hsa_circ_370970,RMVar_hsa_circ_238688,RMVar_hsa_circ_238687,RMVar_hsa_circ_73728,RMVar_hsa_circ_13345,RMVar_hsa_circ_361379,RMVar_hsa_circ_286126,RMVar_hsa_circ_106263,RMVar_hsa_circ_238700,RMVar_hsa_circ_21741,RMVar_hsa_circ_366864,RMVar_hsa_circ_238702,RMVar_hsa_circ_316886,RMVar_hsa_circ_84523,RMVar_hsa_circ_238704,RMVar_hsa_circ_238705 19940 RMVar_ID_19940 Human_SNP_ID_274994943 A-to-I Human chr6 - 43574220 43574220 43574220 CGGCTCACTTCAGCCTTGATTTCTCGAGCTCAAGTGATTCTCCTACCACTTCAGCCTCCTGAGTA CGGCTCACTTCAGCCTTGATTTCTCGAGCTCAGGTGATTCTCCTACCACTTCAGCCTCCTGAGTA T C XPO5 Ensembl:ENSG00000124571 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1287562281 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121992,RMVar_hsa_circ_238652,RMVar_hsa_circ_106263,RMVar_hsa_circ_238702,RMVar_hsa_circ_84523,RMVar_hsa_circ_238705 19941 RMVar_ID_19941 Human_SNP_ID_274998668 A-to-I Human chr6 + 43585723 43585723 43585723 GCTAGGGTGCAATGGTGCAATCTCGGCTCACCACAACCTCCATCTCTTGGATTCAAGTGATTCTC GCTAGGGTGCAATGGTGCAATCTCGGCTCACCGCAACCTCCATCTCTTGGATTCAAGTGATTCTC A G POLH Ensembl:ENSG00000170734 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1286037487 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15674,RMVar_hsa_circ_238706,RMVar_hsa_circ_100753,RMVar_hsa_circ_340216 19942 RMVar_ID_19942 Human_SNP_ID_274998669 A-to-I Human chr6 + 43585723 43585723 43585723 GCTAGGGTGCAATGGTGCAATCTCGGCTCACCACAACCTCCATCTCTTGGATTCAAGTGATTCTC GCTAGGGTGCAATGGTGCAATCTCGGCTCACCTCAACCTCCATCTCTTGGATTCAAGTGATTCTC A T POLH Ensembl:ENSG00000170734 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1286037487 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15674,RMVar_hsa_circ_238706,RMVar_hsa_circ_100753,RMVar_hsa_circ_340216 19943 RMVar_ID_19943 Human_SNP_ID_274999395 A-to-I Human chr6 + 43588577 43588577 43588577 GGGTTCAAGCAGTTCTCCTGCCCCAGCCTCCCAAGTAGCTGGGATTACAGGCATGTATCCACTAC GGGTTCAAGCAGTTCTCCTGCCCCAGCCTCCCGAGTAGCTGGGATTACAGGCATGTATCCACTAC A G POLH Ensembl:ENSG00000170734 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1399001087 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_282209,RMVar_hsa_circ_345350,RMVar_hsa_circ_319711,RMVar_hsa_circ_70478,RMVar_hsa_circ_281526,RMVar_hsa_circ_238710,RMVar_hsa_circ_238711,RMVar_hsa_circ_238709 19944 RMVar_ID_19944 Human_SNP_ID_274999482 A-to-I Human chr6 + 43588967 43588967 43588967 TCACGCCATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACGGGCGCCCGCCACCGCGCCCG TCACGCCATTCTCCTGCCTCAGCCTCCTGAGTGGCTGGGATTACGGGCGCCCGCCACCGCGCCCG A G POLH Ensembl:ENSG00000170734 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1452248790 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_282209,RMVar_hsa_circ_345350,RMVar_hsa_circ_319711,RMVar_hsa_circ_70478,RMVar_hsa_circ_281526,RMVar_hsa_circ_238710,RMVar_hsa_circ_238711,RMVar_hsa_circ_238709 19945 RMVar_ID_19945 Human_SNP_ID_274999665 A-to-I Human chr6 + 43589669 43589667 43589669 CTTTTTTTTTTTTTTGAGATGGAAGTCTCACTATGTTGCCCAGGCTGGAGTGCAGTGGCTATCAG CTTTTTTTTTTTTTTGAGATGGAAGTCTCAC__TGTTGCCCAGGCTGGAGTGCAGTGGCTATCAG CTA C POLH Ensembl:ENSG00000170734 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1246543706 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_8216599 RMVar_hsa_circ_282209,RMVar_hsa_circ_345350,RMVar_hsa_circ_319711,RMVar_hsa_circ_70478,RMVar_hsa_circ_281526,RMVar_hsa_circ_238710,RMVar_hsa_circ_238711,RMVar_hsa_circ_238709 19946 RMVar_ID_19946 Human_SNP_ID_274999830 A-to-I Human chr6 + 43590328 43590328 43590328 TGCAGTGAGCTGAGATCGTACCACTGCACTCCAGCCTCGGCAACAGAGCAAGACTCCATCTTAAA TGCAGTGAGCTGAGATCGTACCACTGCACTCCGGCCTCGGCAACAGAGCAAGACTCCATCTTAAA A G POLH Ensembl:ENSG00000170734 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1045682942 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_282209,RMVar_hsa_circ_345350,RMVar_hsa_circ_319711,RMVar_hsa_circ_70478,RMVar_hsa_circ_281526,RMVar_hsa_circ_238710,RMVar_hsa_circ_238711,RMVar_hsa_circ_238709 19947 RMVar_ID_19947 Human_SNP_ID_274999835 A-to-I Human chr6 + 43590345 43590345 43590345 GTACCACTGCACTCCAGCCTCGGCAACAGAGCAAGACTCCATCTTAAAAAAAAAAAAACAAAAAA GTACCACTGCACTCCAGCCTCGGCAACAGAGCGAGACTCCATCTTAAAAAAAAAAAAACAAAAAA A G POLH Ensembl:ENSG00000170734 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1342035881 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_282209,RMVar_hsa_circ_345350,RMVar_hsa_circ_319711,RMVar_hsa_circ_70478,RMVar_hsa_circ_281526,RMVar_hsa_circ_238710,RMVar_hsa_circ_238711,RMVar_hsa_circ_238709 19948 RMVar_ID_19948 Human_SNP_ID_275000003 A-to-I Human chr6 + 43590913 43590913 43590913 CCACTGTACTCCAGCCTGGGTGGCGACAGAGCAAGACTCTGTCTCAAAAAAAAAAAAGAAAAAAA CCACTGTACTCCAGCCTGGGTGGCGACAGAGCGAGACTCTGTCTCAAAAAAAAAAAAGAAAAAAA A G POLH Ensembl:ENSG00000170734 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1260125943 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_282209,RMVar_hsa_circ_345350,RMVar_hsa_circ_319711,RMVar_hsa_circ_70478,RMVar_hsa_circ_281526,RMVar_hsa_circ_238710,RMVar_hsa_circ_238711,RMVar_hsa_circ_238709 19949 RMVar_ID_19949 Human_SNP_ID_275000149 A-to-I Human chr6 + 43591528 43591528 43591528 TTTAGTAGAGACGGGGTTTCGCCATGTTGGTCAGGCTGGTCTCAAACTCCTGGCATCAAGTTATC TTTAGTAGAGACGGGGTTTCGCCATGTTGGTCTGGCTGGTCTCAAACTCCTGGCATCAAGTTATC A T POLH Ensembl:ENSG00000170734 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs189048171 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_282209,RMVar_hsa_circ_345350,RMVar_hsa_circ_319711,RMVar_hsa_circ_70478,RMVar_hsa_circ_281526,RMVar_hsa_circ_238710,RMVar_hsa_circ_238711,RMVar_hsa_circ_238709 19950 RMVar_ID_19950 Human_SNP_ID_275000159 A-to-I Human chr6 + 43591579 43591579 43591579 GGCATCAAGTTATCCATCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCA GGCATCAAGTTATCCATCTGCCTTGGCCTCCCTAAGTGCTGGGATTACAGGCATGAGCCACCGCA A T POLH Ensembl:ENSG00000170734 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1319177499 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_282209,RMVar_hsa_circ_345350,RMVar_hsa_circ_319711,RMVar_hsa_circ_70478,RMVar_hsa_circ_281526,RMVar_hsa_circ_238710,RMVar_hsa_circ_238711,RMVar_hsa_circ_238709 19951 RMVar_ID_19951 Human_SNP_ID_275000414 A-to-I Human chr6 + 43592597 43592597 43592597 CCACGCCCGGCTAATTTTTTTGTATTTTTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGCA CCACGCCCGGCTAATTTTTTTGTATTTTTTTTGGTAGAGACGGGGTTTCACCGTGTTAGCCAGCA A G POLH Ensembl:ENSG00000170734 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1477180753 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_282209,RMVar_hsa_circ_345350,RMVar_hsa_circ_319711,RMVar_hsa_circ_70478,RMVar_hsa_circ_281526,RMVar_hsa_circ_238710,RMVar_hsa_circ_238711,RMVar_hsa_circ_238709 19952 RMVar_ID_19952 Human_SNP_ID_275000685 A-to-I Human chr6 + 43593812 43593812 43593812 TAAGGCAGGAGAATTACTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCTGAGATTGCGCCACTGT TAAGGCAGGAGAATTACTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCTGAGATTGCGCCACTGT A G POLH Ensembl:ENSG00000170734 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs113914708 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_77 RMVar_hsa_circ_282209,RMVar_hsa_circ_345350,RMVar_hsa_circ_319711,RMVar_hsa_circ_70478,RMVar_hsa_circ_281526,RMVar_hsa_circ_238710,RMVar_hsa_circ_238711,RMVar_hsa_circ_238709 19953 RMVar_ID_19953 Human_SNP_ID_275000878 A-to-I Human chr6 + 43594449 43594449 43594449 CTTTATTTTTAAAAACTACCTTTTGGCCGGGCACAGTGGCTCACGCCTGTAATCCCAGCACTTTG CTTTATTTTTAAAAACTACCTTTTGGCCGGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTTTG A G POLH Ensembl:ENSG00000170734 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1163512560 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_282209,RMVar_hsa_circ_345350,RMVar_hsa_circ_319711,RMVar_hsa_circ_70478,RMVar_hsa_circ_281526,RMVar_hsa_circ_238710,RMVar_hsa_circ_238711,RMVar_hsa_circ_238709 19954 RMVar_ID_19954 Human_SNP_ID_275000880 A-to-I Human chr6 + 43594451 43594451 43594451 TTATTTTTAAAAACTACCTTTTGGCCGGGCACAGTGGCTCACGCCTGTAATCCCAGCACTTTGGG TTATTTTTAAAAACTACCTTTTGGCCGGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG A G POLH Ensembl:ENSG00000170734 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs764244967 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_282209,RMVar_hsa_circ_345350,RMVar_hsa_circ_319711,RMVar_hsa_circ_70478,RMVar_hsa_circ_281526,RMVar_hsa_circ_238710,RMVar_hsa_circ_238711,RMVar_hsa_circ_238709 19955 RMVar_ID_19955 Human_SNP_ID_275001082 A-to-I Human chr6 + 43595334 43595334 43595334 TGTATTTGTATTTTTAGTAGAGACGGGGTTTCACCATGGTGGTCAGGCTGGTCTCAAACTCCTGA TGTATTTGTATTTTTAGTAGAGACGGGGTTTCTCCATGGTGGTCAGGCTGGTCTCAAACTCCTGA A T POLH Ensembl:ENSG00000170734 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs566238814 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_282209,RMVar_hsa_circ_345350,RMVar_hsa_circ_319711,RMVar_hsa_circ_70478,RMVar_hsa_circ_281526,RMVar_hsa_circ_238710,RMVar_hsa_circ_238711,RMVar_hsa_circ_238709 19956 RMVar_ID_19956 Human_SNP_ID_275001148 A-to-I Human chr6 + 43595584 43595583 43595584 CCTGGCTAACATGGTGAAACCCCATCCCTACTAAAAAAAATACAAAAAAATTAGCCGGGCGTGGT CCTGGCTAACATGGTGAAACCCCATCCCTACT_AAAAAAATACAAAAAAATTAGCCGGGCGTGGT TA T POLH Ensembl:ENSG00000170734 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs555305487 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_18077240 RMVar_hsa_circ_282209,RMVar_hsa_circ_345350,RMVar_hsa_circ_319711,RMVar_hsa_circ_70478,RMVar_hsa_circ_281526,RMVar_hsa_circ_238710,RMVar_hsa_circ_238711,RMVar_hsa_circ_238709 19957 RMVar_ID_19957 Human_SNP_ID_275001150 A-to-I Human chr6 + 43595584 43595584 43595584 CCTGGCTAACATGGTGAAACCCCATCCCTACTAAAAAAAATACAAAAAAATTAGCCGGGCGTGGT CCTGGCTAACATGGTGAAACCCCATCCCTACTGAAAAAAATACAAAAAAATTAGCCGGGCGTGGT A G POLH Ensembl:ENSG00000170734 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1168400317 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18077240 RMVar_hsa_circ_282209,RMVar_hsa_circ_345350,RMVar_hsa_circ_319711,RMVar_hsa_circ_70478,RMVar_hsa_circ_281526,RMVar_hsa_circ_238710,RMVar_hsa_circ_238711,RMVar_hsa_circ_238709 19958 RMVar_ID_19958 Human_SNP_ID_275001568 A-to-I Human chr6 + 43597245 43597245 43597245 TCAAGCGAATCTCCTGCCTCAGCCTCCTGAGTAGCTGTGGTTACAGGCCTGCACCACCATGCCCA TCAAGCGAATCTCCTGCCTCAGCCTCCTGAGTCGCTGTGGTTACAGGCCTGCACCACCATGCCCA A C POLH Ensembl:ENSG00000170734 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1380833974 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_282209,RMVar_hsa_circ_345350,RMVar_hsa_circ_319711,RMVar_hsa_circ_70478,RMVar_hsa_circ_281526,RMVar_hsa_circ_238710,RMVar_hsa_circ_238711,RMVar_hsa_circ_238709 19959 RMVar_ID_19959 Human_SNP_ID_275001569 A-to-I Human chr6 + 43597245 43597245 43597245 TCAAGCGAATCTCCTGCCTCAGCCTCCTGAGTAGCTGTGGTTACAGGCCTGCACCACCATGCCCA TCAAGCGAATCTCCTGCCTCAGCCTCCTGAGTTGCTGTGGTTACAGGCCTGCACCACCATGCCCA A T POLH Ensembl:ENSG00000170734 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1380833974 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_282209,RMVar_hsa_circ_345350,RMVar_hsa_circ_319711,RMVar_hsa_circ_70478,RMVar_hsa_circ_281526,RMVar_hsa_circ_238710,RMVar_hsa_circ_238711,RMVar_hsa_circ_238709 19960 RMVar_ID_19960 Human_SNP_ID_275002671 A-to-I Human chr6 + 43601486 43601486 43601486 CAGGGTTTCACCATGTTGGCCAGGCAAATCTCAAACTCTTGACCTCAGGTGATTTGCCCTCCTCA CAGGGTTTCACCATGTTGGCCAGGCAAATCTCGAACTCTTGACCTCAGGTGATTTGCCCTCCTCA A G POLH Ensembl:ENSG00000170734 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs903859649 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_319711,RMVar_hsa_circ_70478,RMVar_hsa_circ_281526,RMVar_hsa_circ_238710,RMVar_hsa_circ_238711,RMVar_hsa_circ_310644,RMVar_hsa_circ_325340,RMVar_hsa_circ_238713,RMVar_hsa_circ_331417,RMVar_hsa_circ_315230,RMVar_hsa_circ_238715,RMVar_hsa_circ_238716 19961 RMVar_ID_19961 Human_SNP_ID_275003112 A-to-I Human chr6 + 43603451 43603451 43603451 TGCACCTGGCCTTAATTTTTTTTTGTAGAGTTAGGGTCTTACTTTGTTGTCCAGGCTGGTCTCAA TGCACCTGGCCTTAATTTTTTTTTGTAGAGTTCGGGTCTTACTTTGTTGTCCAGGCTGGTCTCAA A C POLH Ensembl:ENSG00000170734 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1345156090 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15834322 RMVar_hsa_circ_319711,RMVar_hsa_circ_70478,RMVar_hsa_circ_281526,RMVar_hsa_circ_238710,RMVar_hsa_circ_238711,RMVar_hsa_circ_310644,RMVar_hsa_circ_325340,RMVar_hsa_circ_238713,RMVar_hsa_circ_331417,RMVar_hsa_circ_315230,RMVar_hsa_circ_238715,RMVar_hsa_circ_238716 19962 RMVar_ID_19962 Human_SNP_ID_275003725 A-to-I Human chr6 + 43605817 43605817 43605817 CTTGGCTCACTGCAACCTCCGCCTCTGGGTTCAAGTGATTCTCCTGCCTCACCTTCCCAAGTAGC CTTGGCTCACTGCAACCTCCGCCTCTGGGTTCCAGTGATTCTCCTGCCTCACCTTCCCAAGTAGC A C POLH Ensembl:ENSG00000170734 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1314040906 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_281526,RMVar_hsa_circ_238711,RMVar_hsa_circ_310644,RMVar_hsa_circ_331417,RMVar_hsa_circ_238716,RMVar_hsa_circ_347220,RMVar_hsa_circ_238717 19963 RMVar_ID_19963 Human_SNP_ID_275004089 A-to-I Human chr6 - 43607283 43607283 43607283 TGAGACCACCCTGGCCAACATGGTGAAACCCTATCTCTACTAAAAATACAAAAATTAGCTGGGCG TGAGACCACCCTGGCCAACATGGTGAAACCCTGTCTCTACTAAAAATACAAAAATTAGCTGGGCG T C GTPBP2 Ensembl:ENSG00000172432 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956656570 Functional Loss SNV dbSNP153 33..33 33 - - - 19964 RMVar_ID_19964 Human_SNP_ID_275006054 A-to-I Human chr6 + 43615219 43615219 43615219 CTTGGAGGCGGAGGTTGCATTGAGCTGAGATCATGCTAGTGCGCTCCAGCCTGGGCAACAGAGCG CTTGGAGGCGGAGGTTGCATTGAGCTGAGATCTTGCTAGTGCGCTCCAGCCTGGGCAACAGAGCG A T POLH Ensembl:ENSG00000170734 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1040232734 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125996,RMVar_hsa_circ_238718 19965 RMVar_ID_19965 Human_SNP_ID_275006131 A-to-I Human chr6 + 43615412 43615412 43615412 CATCTCTACTAAAATTACAAAAAAAATTATCCAGGCGTGGTGGTGCACGCCTGTAATCCCAGCTA CATCTCTACTAAAATTACAAAAAAAATTATCCGGGCGTGGTGGTGCACGCCTGTAATCCCAGCTA A G POLH Ensembl:ENSG00000170734 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1364478487 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125996,RMVar_hsa_circ_238718 19966 RMVar_ID_19966 Human_SNP_ID_275006142 A-to-I Human chr6 + 43615434 43615434 43615434 AAAATTATCCAGGCGTGGTGGTGCACGCCTGTAATCCCAGCTACTCAGGAGGCTAAGGCAGGAGA AAAATTATCCAGGCGTGGTGGTGCACGCCTGTGATCCCAGCTACTCAGGAGGCTAAGGCAGGAGA A G POLH Ensembl:ENSG00000170734 Protein coding 3'UTR GSE38233;GSE100210;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,29129909,29796672,31158229,32596459 RNA-Seq:(High) rs1137388 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125996,RMVar_hsa_circ_238718 19967 RMVar_ID_19967 Human_SNP_ID_275006147 A-to-I Human chr6 + 43615448 43615448 43615448 GTGGTGGTGCACGCCTGTAATCCCAGCTACTCAGGAGGCTAAGGCAGGAGAATCACTTGAACCCA GTGGTGGTGCACGCCTGTAATCCCAGCTACTCGGGAGGCTAAGGCAGGAGAATCACTTGAACCCA A G POLH Ensembl:ENSG00000170734 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1141337 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125996,RMVar_hsa_circ_238718 19968 RMVar_ID_19968 Human_SNP_ID_275006148 A-to-I Human chr6 + 43615456 43615456 43615456 GCACGCCTGTAATCCCAGCTACTCAGGAGGCTAAGGCAGGAGAATCACTTGAACCCAGGAGGCAG GCACGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCCAGGAGGCAG A G POLH Ensembl:ENSG00000170734 Protein coding 3'UTR GSE47997;GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 K562 cells&HepG2 cells;cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 23474544,24183664,31158229 RNA-Seq:(High) rs1326121401 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125996,RMVar_hsa_circ_238718 19969 RMVar_ID_19969 Human_SNP_ID_275006255 A-to-I Human chr6 + 43615812 43615812 43615812 CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCACGTGCTACCACACTCAGCTAATTTTT CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTCCAGGCACGTGCTACCACACTCAGCTAATTTTT A C POLH Ensembl:ENSG00000170734 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1002962163 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125996,RMVar_hsa_circ_238718 19970 RMVar_ID_19970 Human_SNP_ID_275006281 A-to-I Human chr6 + 43615907 43615907 43615907 GTTGGCCAGGATGGTCTCGATTGCTTGACCTCATGATCCGCCTGCCTCGACCTCCCAAAGTTGCT GTTGGCCAGGATGGTCTCGATTGCTTGACCTCGTGATCCGCCTGCCTCGACCTCCCAAAGTTGCT A G POLH Ensembl:ENSG00000170734 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1457376034 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_173308 RMVar_hsa_circ_125996,RMVar_hsa_circ_238718 19971 RMVar_ID_19971 Human_SNP_ID_275006466 A-to-I Human chr6 + 43616336 43616336 43616336 TCTCTTTAGGCTGGGTGCGGTTCCTCATGCCTATAATCCCAGCATTTAGGGAGGCTGAGGTGAGT TCTCTTTAGGCTGGGTGCGGTTCCTCATGCCTTTAATCCCAGCATTTAGGGAGGCTGAGGTGAGT A T POLH Ensembl:ENSG00000170734 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1028315005 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_665251 RMVar_hsa_circ_125996,RMVar_hsa_circ_238718 19972 RMVar_ID_19972 Human_SNP_ID_275006479 A-to-I Human chr6 + 43616415 43616415 43616415 CAGGAGTTCGAGACCAGCCTGGGCAAGGTGGCAAAACCCCGTCTCTACTAAAAAAAATTAGCTGG CAGGAGTTCGAGACCAGCCTGGGCAAGGTGGCGAAACCCCGTCTCTACTAAAAAAAATTAGCTGG A G POLH Ensembl:ENSG00000170734 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs9472090 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_78 RMVar_hsa_circ_125996,RMVar_hsa_circ_238718 19973 RMVar_ID_19973 Human_SNP_ID_275006517 A-to-I Human chr6 + 43616530 43616530 43616530 AGAATTGCTTGAACCTGGAAGGTGGAGGTTGCAGTGAGTTGAGATCACACCAATGCACTCCAGCC AGAATTGCTTGAACCTGGAAGGTGGAGGTTGCCGTGAGTTGAGATCACACCAATGCACTCCAGCC A C POLH Ensembl:ENSG00000170734 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs924225468 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125996,RMVar_hsa_circ_238718 19974 RMVar_ID_19974 Human_SNP_ID_275006621 A-to-I Human chr6 + 43616935 43616935 43616935 AATCTTGCCAGGCGTGGTGGTTTATGCCTGTTATCCCAGCACTTTGGGAGGCCAAGGCAGGTGGA AATCTTGCCAGGCGTGGTGGTTTATGCCTGTTGTCCCAGCACTTTGGGAGGCCAAGGCAGGTGGA A G POLH Ensembl:ENSG00000170734 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs768885085 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1941857,Human_miRNA_ID_1944902,Human_miRNA_ID_2085604,Human_miRNA_ID_2116048,Human_miRNA_ID_2199621,Human_miRNA_ID_2202688,Human_miRNA_ID_2315114,Human_miRNA_ID_2318274,Human_miRNA_ID_2321431,Human_miRNA_ID_2324589,Human_miRNA_ID_2327731,Human_miRNA_ID_2518969,Human_miRNA_ID_2522139,Human_miRNA_ID_2773985,Human_miRNA_ID_2815151,Human_miRNA_ID_2821334,Human_miRNA_ID_2827466,Human_miRNA_ID_2830616,Human_miRNA_ID_2834735,Human_miRNA_ID_2840099,Human_miRNA_ID_2845259,Human_miRNA_ID_2848281,Human_miRNA_ID_2862414,Human_miRNA_ID_3112140 RMVar_hsa_circ_125996,RMVar_hsa_circ_238718 19975 RMVar_ID_19975 Human_SNP_ID_275006626 A-to-I Human chr6 + 43616956 43616956 43616956 TTATGCCTGTTATCCCAGCACTTTGGGAGGCCAAGGCAGGTGGACCACGTGAAGTCAGGAGTTCA TTATGCCTGTTATCCCAGCACTTTGGGAGGCCGAGGCAGGTGGACCACGTGAAGTCAGGAGTTCA A G POLH Ensembl:ENSG00000170734 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1200565636 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2217338 RMVar_hsa_circ_125996,RMVar_hsa_circ_238718 19976 RMVar_ID_19976 Human_SNP_ID_275006673 A-to-I Human chr6 + 43617122 43617122 43617122 TGAGGCAGGAGAATCACTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCCGAGATTTCCACTGCAT TGAGGCAGGAGAATCACTTGAACCTGGGAGGCGGAGGTTGCAGTGAGCCGAGATTTCCACTGCAT A G POLH Ensembl:ENSG00000170734 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs911485310 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125996,RMVar_hsa_circ_238718 19977 RMVar_ID_19977 Human_SNP_ID_275006694 A-to-I Human chr6 - 43617180 43617180 43617180 TCTAGAGATGATCTAGTGGGTTTTTTTGAGACAGAGTTACTCTATCGCCCAGGCTGGAATGCAGT TCTAGAGATGATCTAGTGGGTTTTTTTGAGACGGAGTTACTCTATCGCCCAGGCTGGAATGCAGT T C GTPBP2 Ensembl:ENSG00000172432 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs896550530 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1218002 19978 RMVar_ID_19978 Human_SNP_ID_275006742 A-to-I Human chr6 + 43617371 43617367 43617372 AATGTGGGTCAGGTGTGGTGGCTCATGCCTGTAATCCCACACTTTGGGAGGCCAAGGTGGGCGGA AATGTGGGTCAGGTGTGGTGGCTCATGCC_____TCCCACACTTTGGGAGGCCAAGGTGGGCGGA CTGTAA C POLH Ensembl:ENSG00000170734 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1372390327 Functional Loss DEL dbSNP153 30..34 33 - - - RMVar_hsa_circ_125996,RMVar_hsa_circ_238718 19979 RMVar_ID_19979 Human_SNP_ID_275006758 A-to-I Human chr6 + 43617392 43617392 43617392 CTCATGCCTGTAATCCCACACTTTGGGAGGCCAAGGTGGGCGGATCACTTGAGGCTGGGAGTTTG CTCATGCCTGTAATCCCACACTTTGGGAGGCCGAGGTGGGCGGATCACTTGAGGCTGGGAGTTTG A G POLH Ensembl:ENSG00000170734 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1363964592 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125996,RMVar_hsa_circ_238718 19980 RMVar_ID_19980 Human_SNP_ID_275006773 A-to-I Human chr6 + 43617475 43617475 43617475 TGGGGAAAACCCATCTCTACAAAAAATAACAAAAATTAGGTGTGTGTGGTGACGCATGCGTGTAA TGGGGAAAACCCATCTCTACAAAAAATAACAATAATTAGGTGTGTGTGGTGACGCATGCGTGTAA A T POLH Ensembl:ENSG00000170734 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs555641345 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24164247 RMVar_hsa_circ_125996,RMVar_hsa_circ_238718 19981 RMVar_ID_19981 Human_SNP_ID_275006841 A-to-I Human chr6 - 43617695 43617695 43617695 TTGATCTCTTGACCTCGTGATACACCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAG TTGATCTCTTGACCTCGTGATACACCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAG T C GTPBP2 Ensembl:ENSG00000172432 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1387142381 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_172383 19982 RMVar_ID_19982 Human_SNP_ID_275006851 A-to-I Human chr6 + 43617744 43617744 43617744 GAGGTCAAGAGATCAAGGCCATCCTGGCCAACATGGTGAAACCCCGTCTCTACTGAAAATACAAC GAGGTCAAGAGATCAAGGCCATCCTGGCCAACGTGGTGAAACCCCGTCTCTACTGAAAATACAAC A G POLH Ensembl:ENSG00000170734 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1199951818 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125996,RMVar_hsa_circ_238718 19983 RMVar_ID_19983 Human_SNP_ID_275006871 A-to-I Human chr6 + 43617806 43617806 43617806 AACTGGGCGTGGTGGTGCACGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGAAGAATTGCT AACTGGGCGTGGTGGTGCACGCCTGTAGTCCCGGCTACTTGGGAGGCTGAGGCAGAAGAATTGCT A G POLH Ensembl:ENSG00000170734 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1006495615 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125996,RMVar_hsa_circ_238718 19984 RMVar_ID_19984 Human_SNP_ID_275006873 A-to-I Human chr6 + 43617810 43617810 43617810 GGGCGTGGTGGTGCACGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGAAGAATTGCTTGAC GGGCGTGGTGGTGCACGCCTGTAGTCCCAGCTTCTTGGGAGGCTGAGGCAGAAGAATTGCTTGAC A T POLH Ensembl:ENSG00000170734 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1393714103 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125996,RMVar_hsa_circ_238718 19985 RMVar_ID_19985 Human_SNP_ID_275006905 A-to-I Human chr6 + 43617906 43617906 43617906 CGTGCCACTGCACTGCACCCTGGCGACACAGCAAGACTGTCTCAAAAAAAAAAAAATTCCCAATG CGTGCCACTGCACTGCACCCTGGCGACACAGCGAGACTGTCTCAAAAAAAAAAAAATTCCCAATG A G POLH Ensembl:ENSG00000170734 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1300366478 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125996,RMVar_hsa_circ_238718 19986 RMVar_ID_19986 Human_SNP_ID_275007011 A-to-I Human chr6 + 43618330 43618330 43618330 AGCGTGCACCACCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGACAGGTTTTCACCATGTTGG AGCGTGCACCACCATGCCCAGCTAATTTTTGTGTTTTTAGTAGAGACAGGTTTTCACCATGTTGG A G POLH Ensembl:ENSG00000170734 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1040025248 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125996,RMVar_hsa_circ_238718 19987 RMVar_ID_19987 Human_SNP_ID_275007033 A-to-I Human chr6 + 43618412 43618412 43618412 TAGACCTCGTGATCCATCCGCCTCGGCCTCCCAAAGTGCTGGGATTATAGGCATGAGCCACCACG TAGACCTCGTGATCCATCCGCCTCGGCCTCCCGAAGTGCTGGGATTATAGGCATGAGCCACCACG A G POLH Ensembl:ENSG00000170734 Protein coding 3'UTR GSE100210;GSE99789;GSE99789 HepG2 cell line;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109 - 29129909,29796672,29796672 RNA-Seq:(High) rs1026372453 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125996,RMVar_hsa_circ_238718 19988 RMVar_ID_19988 Human_SNP_ID_275007034 A-to-I Human chr6 + 43618413 43618413 43618413 AGACCTCGTGATCCATCCGCCTCGGCCTCCCAAAGTGCTGGGATTATAGGCATGAGCCACCACGC AGACCTCGTGATCCATCCGCCTCGGCCTCCCAGAGTGCTGGGATTATAGGCATGAGCCACCACGC A G POLH Ensembl:ENSG00000170734 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1489047924 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125996,RMVar_hsa_circ_238718 19989 RMVar_ID_19989 Human_SNP_ID_275007040 A-to-I Human chr6 + 43618435 43618435 43618435 CGGCCTCCCAAAGTGCTGGGATTATAGGCATGAGCCACCACGCCCAGCCTATAGTACTGTATTCT CGGCCTCCCAAAGTGCTGGGATTATAGGCATGGGCCACCACGCCCAGCCTATAGTACTGTATTCT A G POLH Ensembl:ENSG00000170734 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1388872088 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125996,RMVar_hsa_circ_238718 19990 RMVar_ID_19990 Human_SNP_ID_275007093 A-to-I Human chr6 + 43618648 43618646 43618648 TCCCATACATATACCCAAACTTCTATTTTTTTATGTGACGGAGTTTCTCTCATCGCCCCGGCTGG TCCCATACATATACCCAAACTTCTATTTTTT__TGTGACGGAGTTTCTCTCATCGCCCCGGCTGG TTA T POLH Ensembl:ENSG00000170734 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1245784369 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_15834429,Human_RBP_ID_23314764 RMVar_hsa_circ_125996,RMVar_hsa_circ_238718 19991 RMVar_ID_19991 Human_SNP_ID_275007094 A-to-I Human chr6 + 43618648 43618648 43618648 TCCCATACATATACCCAAACTTCTATTTTTTTATGTGACGGAGTTTCTCTCATCGCCCCGGCTGG TCCCATACATATACCCAAACTTCTATTTTTTTTTGTGACGGAGTTTCTCTCATCGCCCCGGCTGG A T POLH Ensembl:ENSG00000170734 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1016537347 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15834429,Human_RBP_ID_23314764 RMVar_hsa_circ_125996,RMVar_hsa_circ_238718 19992 RMVar_ID_19992 Human_SNP_ID_275007106 A-to-I Human chr6 + 43618686 43618686 43618686 CGGAGTTTCTCTCATCGCCCCGGCTGGAATGCAATGGCACGATCTCGGCTCACTGCAACCTCCGC CGGAGTTTCTCTCATCGCCCCGGCTGGAATGCCATGGCACGATCTCGGCTCACTGCAACCTCCGC A C POLH Ensembl:ENSG00000170734 Protein coding 3'UTR GSE47997;GSE38233;GSE99789 K562 cells&HepG2 cells;cultured B-cells;esophageal squamous carcinoma cells,EC109 - 23474544,24183664,29796672 RNA-Seq:(High) rs1323902177 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15834431 RMVar_hsa_circ_125996,RMVar_hsa_circ_238718 19993 RMVar_ID_19993 Human_SNP_ID_275007107 A-to-I Human chr6 + 43618686 43618686 43618686 CGGAGTTTCTCTCATCGCCCCGGCTGGAATGCAATGGCACGATCTCGGCTCACTGCAACCTCCGC CGGAGTTTCTCTCATCGCCCCGGCTGGAATGCGATGGCACGATCTCGGCTCACTGCAACCTCCGC A G POLH Ensembl:ENSG00000170734 Protein coding 3'UTR GSE47997;GSE38233;GSE99789 K562 cells&HepG2 cells;cultured B-cells;esophageal squamous carcinoma cells,EC109 - 23474544,24183664,29796672 RNA-Seq:(High) rs1323902177 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15834431 RMVar_hsa_circ_125996,RMVar_hsa_circ_238718 19994 RMVar_ID_19994 Human_SNP_ID_275007140 A-to-I Human chr6 + 43618796 43618796 43618796 GGGATTATAGGCATGCACCATCACGCCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCG GGGATTATAGGCATGCACCATCACGCCTGGCTCATTTTTGTATTTTTAGTAGAGATGGGGTTTCG A C POLH Ensembl:ENSG00000170734 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1470868517 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125996,RMVar_hsa_circ_238718 19995 RMVar_ID_19995 Human_SNP_ID_275007143 A-to-I Human chr6 + 43618811 43618811 43618811 CACCATCACGCCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCGCCACGTTGGCCAGGC CACCATCACGCCTGGCTAATTTTTGTATTTTTCGTAGAGATGGGGTTTCGCCACGTTGGCCAGGC A C POLH Ensembl:ENSG00000170734 Protein coding 3'UTR GSE38233;GSE99789 cultured B-cells;esophageal squamous carcinoma cells,EC109 - 24183664,29796672 RNA-Seq:(High) rs1053106288 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26009262 RMVar_hsa_circ_125996,RMVar_hsa_circ_238718 19996 RMVar_ID_19996 Human_SNP_ID_275007269 A-to-I Human chr6 + 43619257 43619257 43619257 ATGGTGGCTTATGCCTGTAGTCGTACCTACTCAGGAGGCTGAGGTTGGGAGGATCACCTGAATCT ATGGTGGCTTATGCCTGTAGTCGTACCTACTCCGGAGGCTGAGGTTGGGAGGATCACCTGAATCT A C POLH Ensembl:ENSG00000170734 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1000725834 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125996,RMVar_hsa_circ_238718 19997 RMVar_ID_19997 Human_SNP_ID_275007284 A-to-I Human chr6 - 43619303 43619303 43619303 TGGAGTGCAGCGGCACAATCATGGCTTATTGCAGCCCCAAACTCCCAGATTCAGGTGATCCTCCC TGGAGTGCAGCGGCACAATCATGGCTTATTGCCGCCCCAAACTCCCAGATTCAGGTGATCCTCCC T G GTPBP2 Ensembl:ENSG00000172432 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs970602180 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17576348 19998 RMVar_ID_19998 Human_SNP_ID_275012069 A-to-I Human chr6 + 43636947 43636947 43636947 TTGCCCAGGCTAGAGTGCAGTGGCGAGATCTCAGCTCACTGCAACCTCCGCCTCCCAGGTTCAAG TTGCCCAGGCTAGAGTGCAGTGGCGAGATCTCGGCTCACTGCAACCTCCGCCTCCCAGGTTCAAG A G MAD2L1BP Ensembl:ENSG00000124688 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs112662040 Functional Loss SNV dbSNP153 33..33 33 - - - 19999 RMVar_ID_19999 Human_SNP_ID_275012137 A-to-I Human chr6 + 43637198 43637198 43637198 GCGATTCTCATGCCTCAGCCTCCCCAGTAGCTAGGATTACAGGCACGTGCCACCATGCCCAGCTT GCGATTCTCATGCCTCAGCCTCCCCAGTAGCTGGGATTACAGGCACGTGCCACCATGCCCAGCTT A G MAD2L1BP Ensembl:ENSG00000124688 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1271413663 Functional Loss SNV dbSNP153 33..33 33 - - - 20000 RMVar_ID_20000 Human_SNP_ID_275012369 A-to-I Human chr6 + 43638037 43638037 43638037 TCTCCTGCCTCAGCCTCGAAGTAGCTGGGATTACAGGCATGTGCCACCACACCTGGTTAAATTTT TCTCCTGCCTCAGCCTCGAAGTAGCTGGGATTGCAGGCATGTGCCACCACACCTGGTTAAATTTT A G MAD2L1BP Ensembl:ENSG00000124688 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1298721905 Functional Loss SNV dbSNP153 33..33 33 - - - 20001 RMVar_ID_20001 Human_SNP_ID_275012422 A-to-I Human chr6 + 43638276 43638276 43638276 GTTGGCCAGGCTGGTCTCGAAGTCCTGACCTCAGGTTATCCACCTGCCTCAGCCTCCCAAAGTGT GTTGGCCAGGCTGGTCTCGAAGTCCTGACCTCGGGTTATCCACCTGCCTCAGCCTCCCAAAGTGT A G MAD2L1BP Ensembl:ENSG00000124688 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1045037820 Functional Loss SNV dbSNP153 33..33 33 - - - 20002 RMVar_ID_20002 Human_SNP_ID_275012558 A-to-I Human chr6 + 43638777 43638777 43638777 GAGATTGCGCCACTGTACTCCAGCCTGGGCGAAAGAGCGAAACTCTGTCTCAAAAAAAAAAAAAA GAGATTGCGCCACTGTACTCCAGCCTGGGCGACAGAGCGAAACTCTGTCTCAAAAAAAAAAAAAA A C MAD2L1BP Ensembl:ENSG00000124688 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1001241494 Functional Loss SNV dbSNP153 33..33 33 - - - 20003 RMVar_ID_20003 Human_SNP_ID_275012559 A-to-I Human chr6 + 43638777 43638777 43638777 GAGATTGCGCCACTGTACTCCAGCCTGGGCGAAAGAGCGAAACTCTGTCTCAAAAAAAAAAAAAA GAGATTGCGCCACTGTACTCCAGCCTGGGCGAGAGAGCGAAACTCTGTCTCAAAAAAAAAAAAAA A G MAD2L1BP Ensembl:ENSG00000124688 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1001241494 Functional Loss SNV dbSNP153 33..33 33 - - - 20004 RMVar_ID_20004 Human_SNP_ID_275012560 A-to-I Human chr6 + 43638777 43638777 43638777 GAGATTGCGCCACTGTACTCCAGCCTGGGCGAAAGAGCGAAACTCTGTCTCAAAAAAAAAAAAAA GAGATTGCGCCACTGTACTCCAGCCTGGGCGATAGAGCGAAACTCTGTCTCAAAAAAAAAAAAAA A T MAD2L1BP Ensembl:ENSG00000124688 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1001241494 Functional Loss SNV dbSNP153 33..33 33 - - - 20005 RMVar_ID_20005 Human_SNP_ID_275012677 A-to-I Human chr6 + 43639269 43639269 43639269 TCAGGCTATTCTCCTGCCTCAGCCTCCCTAGTAGCTGGGACTACAGGCATCCACCACCACACTCG TCAGGCTATTCTCCTGCCTCAGCCTCCCTAGTTGCTGGGACTACAGGCATCCACCACCACACTCG A T MAD2L1BP Ensembl:ENSG00000124688 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1487013451 Functional Loss SNV dbSNP153 33..33 33 - - - 20006 RMVar_ID_20006 Human_SNP_ID_275012679 A-to-I Human chr6 + 43639279 43639279 43639279 CTCCTGCCTCAGCCTCCCTAGTAGCTGGGACTACAGGCATCCACCACCACACTCGGCTAATTTTT CTCCTGCCTCAGCCTCCCTAGTAGCTGGGACTGCAGGCATCCACCACCACACTCGGCTAATTTTT A G MAD2L1BP Ensembl:ENSG00000124688 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs762851263 Functional Loss SNV dbSNP153 33..33 33 - - - 20007 RMVar_ID_20007 Human_SNP_ID_275012737 A-to-I Human chr6 + 43639421 43639421 43639421 TCGGCCTCTCAAAGTGCTGGGATTACAGGCGTAAGCCACTGCGCCCAGCCAACTCTTCATCTTCT TCGGCCTCTCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCGCCCAGCCAACTCTTCATCTTCT A G MAD2L1BP Ensembl:ENSG00000124688 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1249721121 Functional Loss SNV dbSNP153 33..33 33 - - - 20008 RMVar_ID_20008 Human_SNP_ID_275106266 A-to-I Human chr6 + 44014735 44014735 44014735 GTTGCCCAGGCTGGTCTGTAGCTCCTGGGCTCAAGTGATCCTCTCACCTTGGCCTCCCAAAGTGC GTTGCCCAGGCTGGTCTGTAGCTCCTGGGCTCCAGTGATCCTCTCACCTTGGCCTCCCAAAGTGC A C lnc-C6orf223-1 RNACentral:URS00009C3AE1 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs527649047 Functional Loss SNV dbSNP153 33..33 33 - - - 20009 RMVar_ID_20009 Human_SNP_ID_275111168 A-to-I Human chr6 - 44037474 44037474 44037474 ATTCGGGACGCTGAGACATGAGACTTGCTTGAACACAGGAGGTGGAGGTTGCAGTGAGCCGAGAT ATTCGGGACGCTGAGACATGAGACTTGCTTGACCACAGGAGGTGGAGGTTGCAGTGAGCCGAGAT T G AL109615.3 Ensembl:ENSG00000237686 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs953939344 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106005,RMVar_hsa_circ_238732 20010 RMVar_ID_20010 Human_SNP_ID_275111172 A-to-I Human chr6 - 44037493 44037493 44037493 CACACCTGTAATCCCAGCTATTCGGGACGCTGAGACATGAGACTTGCTTGAACACAGGAGGTGGA CACACCTGTAATCCCAGCTATTCGGGACGCTGCGACATGAGACTTGCTTGAACACAGGAGGTGGA T G AL109615.3 Ensembl:ENSG00000237686 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1325749227 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106005,RMVar_hsa_circ_238732 20011 RMVar_ID_20011 Human_SNP_ID_275124460 A-to-I Human chr6 - 44091449 44091449 44091449 TGTGGTGAGCGGAGATCATGCCACTGTACTCCAACCTGGGTGACAGAGTGAGACCCTATCTCAAA TGTGGTGAGCGGAGATCATGCCACTGTACTCCGACCTGGGTGACAGAGTGAGACCCTATCTCAAA T C AL109615.4 Ensembl:ENSG00000287562 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348950588 Functional Loss SNV dbSNP153 33..33 33 - - - 20012 RMVar_ID_20012 Human_SNP_ID_275125226 A-to-I Human chr6 - 44094813 44094813 44094813 TGATGGAATCTCAGCTTGGCTACTCACCAGCTATGCGACCCTGGGCAAGTTACTTAACCTCTGAG TGATGGAATCTCAGCTTGGCTACTCACCAGCTGTGCGACCCTGGGCAAGTTACTTAACCTCTGAG T C AL109615.4 Ensembl:ENSG00000287562 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs763342833 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8645914,Human_RBP_ID_21346490,Human_RBP_ID_24164376 20013 RMVar_ID_20013 Human_SNP_ID_275125412 A-to-I Human chr6 - 44095544 44095544 44095544 GTGGTGGCACACGCCTGTAGTTTCAGCTACTCAGGAGGCTGAGGCAGGAAAATCGCTTGAACTCG GTGGTGGCACACGCCTGTAGTTTCAGCTACTCGGGAGGCTGAGGCAGGAAAATCGCTTGAACTCG T C AL109615.4 Ensembl:ENSG00000287562 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1396926719 Functional Loss SNV dbSNP153 33..33 33 - - - 20014 RMVar_ID_20014 Human_SNP_ID_275126398 A-to-I Human chr6 - 44099114 44099114 44099114 CTGCCTCCATACGCCGGGTTCAAGGTGTCTCAACCTCCTGCATAGCTGGGATCACAGGCCACCAT CTGCCTCCATACGCCGGGTTCAAGGTGTCTCACCCTCCTGCATAGCTGGGATCACAGGCCACCAT T G RF00017-4486 RNACentral:URS000090F764 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs553317419 Functional Loss SNV dbSNP153 33..33 33 - - - 20015 RMVar_ID_20015 Human_SNP_ID_275130948 A-to-I Human chr6 - 44117740 44117740 44117740 GGATCACCTGAGCTTGGGGAGTTCGGGACTGCAGTGAGCTGCAGTTGCACCACTACATTCCAGCA GGATCACCTGAGCTTGGGGAGTTCGGGACTGCCGTGAGCTGCAGTTGCACCACTACATTCCAGCA T G MRPL14 Ensembl:ENSG00000180992 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1431662668 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7609662 RMVar_hsa_circ_77917,RMVar_hsa_circ_238733 20016 RMVar_ID_20016 Human_SNP_ID_275134477 A-to-I Human chr6 + 44130949 44130949 44130949 TACTACTACTTTTTTTTTTGAGATGGAGTCTCACTCTGTCGCCCAGGCTGGAGTGCAGTGGCATG TACTACTACTTTTTTTTTTGAGATGGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCATG A G TMEM63B Ensembl:ENSG00000137216 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459693961 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112748,RMVar_hsa_circ_238734 20017 RMVar_ID_20017 Human_SNP_ID_275134509 A-to-I Human chr6 + 44131103 44131103 44131103 CCACACCCAGCTAATTTTTGTATTTTTTTAGTAGAGACGGGGTTTCACTGTGTTGGCCAGGCTGG CCACACCCAGCTAATTTTTGTATTTTTTTAGTGGAGACGGGGTTTCACTGTGTTGGCCAGGCTGG A G TMEM63B Ensembl:ENSG00000137216 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1039833848 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112748,RMVar_hsa_circ_238734 20018 RMVar_ID_20018 Human_SNP_ID_275134671 A-to-I Human chr6 + 44131700 44131700 44131700 AAGATCGCGCCACTGCACTCCACTCTGGTGACAGAGCGAGACTCCGTCTCAAAAAAATACACAAC AAGATCGCGCCACTGCACTCCACTCTGGTGACGGAGCGAGACTCCGTCTCAAAAAAATACACAAC A G TMEM63B Ensembl:ENSG00000137216 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1271911322 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112748,RMVar_hsa_circ_238734 20019 RMVar_ID_20019 Human_SNP_ID_275138038 A-to-I Human chr6 + 44144612 44144612 44144612 CATTTAAAAAAAAAAACAATTTTTTTTGAGACAGAGTCTCACTCTGTCTCCCTGGCTGGAGTGCT CATTTAAAAAAAAAAACAATTTTTTTTGAGACGGAGTCTCACTCTGTCTCCCTGGCTGGAGTGCT A G TMEM63B Ensembl:ENSG00000137216 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs945869803 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63840,RMVar_hsa_circ_32899,RMVar_hsa_circ_80895,RMVar_hsa_circ_350829,RMVar_hsa_circ_238740,RMVar_hsa_circ_238741,RMVar_hsa_circ_238743,RMVar_hsa_circ_116882 20020 RMVar_ID_20020 Human_SNP_ID_275138507 A-to-I Human chr6 + 44146568 44146568 44146568 CACCTCCCGGGTTCGAGCAATTCTTCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCACGTG CACCTCCCGGGTTCGAGCAATTCTTCTGCCTCGGCCTCCTGAGTAGCTGGGACTACAGGCACGTG A G TMEM63B Ensembl:ENSG00000137216 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1381668400 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_170000 RMVar_hsa_circ_63840,RMVar_hsa_circ_32899,RMVar_hsa_circ_80895,RMVar_hsa_circ_350829,RMVar_hsa_circ_238740,RMVar_hsa_circ_238741,RMVar_hsa_circ_238743,RMVar_hsa_circ_116882 20021 RMVar_ID_20021 Human_SNP_ID_275163764 A-to-I Human chr6 + 44240313 44240313 44240313 CTACAAAAAAAATTTAAAAATCAGTCAGGCCTAGTGGCACATGCCTGTAGTTCCAGCTGCTTGGG CTACAAAAAAAATTTAAAAATCAGTCAGGCCTGGTGGCACATGCCTGTAGTTCCAGCTGCTTGGG A G lnc-SLC29A1-2,RF00017-4633 RNACentral:URS00008B93E7,RNACentral:URS00009644F0 lincRNA,SRP RNA exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs529898516 Functional Loss SNV dbSNP153 33..33 33 - - - 20022 RMVar_ID_20022 Human_SNP_ID_275168793 A-to-I Human chr6 - 44254225 44254225 44254225 AGGAAAGGGGATGCAGAGCCCTGCCCAGCACCACCACCTCCTATGCTCCTGGATCCCTAGGCTCT AGGAAAGGGGATGCAGAGCCCTGCCCAGCACCCCCACCTCCTATGCTCCTGGATCCCTAGGCTCT T G SLC35B2,MIR4647 Ensembl:ENSG00000157593,Ensembl:ENSG00000284427 Protein coding,miRNA exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1064730 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_665499,Human_RBP_ID_5152686,Human_RBP_ID_17664151,Human_RBP_ID_22514878,Human_RBP_ID_26539572,Human_RBP_ID_27102676,Human_RBP_ID_27350106,Human_RBP_ID_27527073 Human_miRNA_ID_2992656,Human_miRNA_ID_3142914 RMVar_hsa_circ_85787,RMVar_hsa_circ_238779 20023 RMVar_ID_20023 Human_SNP_ID_275168961 A-to-I Human chr6 - 44254644 44254644 44254644 AATAGGACCCTCCCACCATCCCCTTCTGCTGTAACCTCTGAGGGAGCTGGCTGAAAGGGCAAAAT AATAGGACCCTCCCACCATCCCCTTCTGCTGTTACCTCTGAGGGAGCTGGCTGAAAGGGCAAAAT T A SLC35B2 Ensembl:ENSG00000157593 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs542627400 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_665512,Human_RBP_ID_790541,Human_RBP_ID_4892487,Human_RBP_ID_8646075,Human_RBP_ID_17663789,Human_RBP_ID_18077522,Human_RBP_ID_27525247 RMVar_hsa_circ_85787,RMVar_hsa_circ_238779 20024 RMVar_ID_20024 Human_SNP_ID_275184360 A-to-I Human chr6 - 44308391 44308391 44308391 GGGATTACAGGCACCCGCCAACACACCTGACTAATTTTTGTATTTTTAGTACAGATGGGGTTTCA GGGATTACAGGCACCCGCCAACACACCTGACTGATTTTTGTATTTTTAGTACAGATGGGGTTTCA T C AARS2 Ensembl:ENSG00000124608 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs370230893 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104129,RMVar_hsa_circ_238787,RMVar_hsa_circ_238792,RMVar_hsa_circ_92010,RMVar_hsa_circ_238800,RMVar_hsa_circ_113719 20025 RMVar_ID_20025 Human_SNP_ID_275184492 A-to-I Human chr6 - 44308893 44308893 44308893 CAGAGTGGTGAGAAGAGTTCTCAGGGCTGGGCACGGTGGCTCACTCCTGTAATCCCAGCACTTGG CAGAGTGGTGAGAAGAGTTCTCAGGGCTGGGCGCGGTGGCTCACTCCTGTAATCCCAGCACTTGG T C AARS2 Ensembl:ENSG00000124608 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1192082391 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15836703 RMVar_hsa_circ_104129,RMVar_hsa_circ_238787,RMVar_hsa_circ_238792,RMVar_hsa_circ_92010,RMVar_hsa_circ_238800,RMVar_hsa_circ_113719 20026 RMVar_ID_20026 Human_SNP_ID_275204299 A-to-I Human chr6 + 44391746 44391746 44391746 AATGTAGAAATTGGCCAGGCGTGGTGGCTCACATCTGTAAGCCTAGCACTTCGGGAGGCCAAGGC AATGTAGAAATTGGCCAGGCGTGGTGGCTCACGTCTGTAAGCCTAGCACTTCGGGAGGCCAAGGC A G CDC5L Ensembl:ENSG00000096401 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1248743932 Functional Loss SNV dbSNP153 33..33 33 - - - 20027 RMVar_ID_20027 Human_SNP_ID_275204769 A-to-I Human chr6 + 44393688 44393688 44393688 CTCTACTTTAGAATCCCTTTTTTTTTTGAGACAAGGTCTTGCTCTGTTACCCAGGCTGGAATGAA CTCTACTTTAGAATCCCTTTTTTTTTTGAGACGAGGTCTTGCTCTGTTACCCAGGCTGGAATGAA A G CDC5L Ensembl:ENSG00000096401 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1276915467 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4390,RMVar_hsa_circ_72380,RMVar_hsa_circ_89464,RMVar_hsa_circ_238807 20028 RMVar_ID_20028 Human_SNP_ID_275217829 A-to-I Human chr6 + 44449399 44449399 44449399 CACTGAGGCCAGGGGTGGTGAGTCATGCCTGTAATCCTAGCACTTTGGGAGGCCAAGGTGGGAGG CACTGAGGCCAGGGGTGGTGAGTCATGCCTGTGATCCTAGCACTTTGGGAGGCCAAGGTGGGAGG A G CDC5L Ensembl:ENSG00000096401 Protein coding 3'UTR GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-Seq:(High) rs1199078568 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26540234 20029 RMVar_ID_20029 Human_SNP_ID_275217974 A-to-I Human chr6 + 44450064 44450064 44450064 TTTTGTGTTTTTAGTAGAGATGGGGTTTTGCTATGTTGGCCAGGCTGGTCTTGAATTCCTGACCT TTTTGTGTTTTTAGTAGAGATGGGGTTTTGCTGTGTTGGCCAGGCTGGTCTTGAATTCCTGACCT A G CDC5L Ensembl:ENSG00000096401 Protein coding 3'UTR GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1009809237 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26009940,Human_RBP_ID_26539576 20030 RMVar_ID_20030 Human_SNP_ID_275217989 A-to-I Human chr6 + 44450138 44450138 44450138 CACCTACCTCGGCCTCCCAAAGTGCTAGAATTACAGGTGTGAGCCACCATGCCCAGCCTGGTTAT CACCTACCTCGGCCTCCCAAAGTGCTAGAATTGCAGGTGTGAGCCACCATGCCCAGCCTGGTTAT A G CDC5L Ensembl:ENSG00000096401 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs796502479 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_665611,Human_RBP_ID_26539576 20031 RMVar_ID_20031 Human_SNP_ID_44996945 A-to-I Human chr1 - 197040700 197040700 197040700 CATGCACATTATCTTTTACTGAAATGGAAAAGAATAATTTACTTCTGAAATGGGATTTTGACAAT CATGCACATTATCTTTTACTGAAATGGAAAAGCATAATTTACTTCTGAAATGGGATTTTGACAAT T G F13B Ensembl:ENSG00000143278 Protein coding CDS GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1558302023 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_169470,Human_Splice_Rec_169492,Human_Splice_Rec_169496 RMVar_hsa_circ_53971,RMVar_hsa_circ_57069,RMVar_hsa_circ_56217 20032 RMVar_ID_20032 Human_SNP_ID_45011158 A-to-I Human chr1 - 197098062 197098062 197098062 TCCCTCTTAACGCTATGTTGGCTTCTCTTGTCAATGTCTGTAAATTTTGATGTTCTTCAGGTGTG TCCCTCTTAACGCTATGTTGGCTTCTCTTGTCCATGTCTGTAAATTTTGATGTTCTTCAGGTGTG T G ASPM Ensembl:ENSG00000066279 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251163123 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19248373 RMVar_hsa_circ_66661,RMVar_hsa_circ_75361,RMVar_hsa_circ_94722,RMVar_hsa_circ_138594,RMVar_hsa_circ_56839,RMVar_hsa_circ_265806,RMVar_hsa_circ_70759 20033 RMVar_ID_20033 Human_SNP_ID_45011322 A-to-I Human chr1 - 197098688 197098688 197098688 AAATTCACAGACATTGACAAGAGAAGCCAACAAGGTGTTAAGAGGGAAAGAAGAAAGGTAAGAGA AAATTCACAGACATTGACAAGAGAAGCCAACATGGTGTTAAGAGGGAAAGAAGAAAGGTAAGAGA T A ASPM Ensembl:ENSG00000066279 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1048185877 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66661,RMVar_hsa_circ_75361,RMVar_hsa_circ_94722,RMVar_hsa_circ_138594,RMVar_hsa_circ_56839,RMVar_hsa_circ_265806,RMVar_hsa_circ_70759 20034 RMVar_ID_20034 Human_SNP_ID_45011328 A-to-I Human chr1 - 197098720 197098720 197098720 AGGGCCTGGGACTTGAGCCCTGAAGAACATCAAAATTCACAGACATTGACAAGAGAAGCCAACAA AGGGCCTGGGACTTGAGCCCTGAAGAACATCAGAATTCACAGACATTGACAAGAGAAGCCAACAA T C ASPM Ensembl:ENSG00000066279 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049397977 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8045265 RMVar_hsa_circ_66661,RMVar_hsa_circ_75361,RMVar_hsa_circ_94722,RMVar_hsa_circ_138594,RMVar_hsa_circ_56839,RMVar_hsa_circ_265806,RMVar_hsa_circ_70759 20035 RMVar_ID_20035 Human_SNP_ID_45011329 A-to-I Human chr1 - 197098726 197098726 197098726 ACAAAGAGGGCCTGGGACTTGAGCCCTGAAGAACATCAAAATTCACAGACATTGACAAGAGAAGC ACAAAGAGGGCCTGGGACTTGAGCCCTGAAGAGCATCAAAATTCACAGACATTGACAAGAGAAGC T C ASPM Ensembl:ENSG00000066279 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1558326978 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8045265 RMVar_hsa_circ_66661,RMVar_hsa_circ_75361,RMVar_hsa_circ_94722,RMVar_hsa_circ_138594,RMVar_hsa_circ_56839,RMVar_hsa_circ_265806,RMVar_hsa_circ_70759 20036 RMVar_ID_20036 Human_SNP_ID_45021691 A-to-I Human chr1 - 197138579 197138579 197138579 AAGTGTGAACTCCTAGTGGGGCGTGGTGGCTCATGCCTGTGATCCCAGCACTTTGGGAGGCTGAG AAGTGTGAACTCCTAGTGGGGCGTGGTGGCTCTTGCCTGTGATCCCAGCACTTTGGGAGGCTGAG T A ASPM Ensembl:ENSG00000066279 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041842786 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265806,RMVar_hsa_circ_357987,RMVar_hsa_circ_268720,RMVar_hsa_circ_52323,RMVar_hsa_circ_78214,RMVar_hsa_circ_138601,RMVar_hsa_circ_370738,RMVar_hsa_circ_138609,RMVar_hsa_circ_375689,RMVar_hsa_circ_68502,RMVar_hsa_circ_138610,RMVar_hsa_circ_59770 20037 RMVar_ID_20037 Human_SNP_ID_45041695 A-to-I Human chr1 - 197223065 197223065 197223065 ACGCAAGGTTATAGGGACTTGCTGGGTTCTTCACTTATTTTGCCTCAAAGATAGTCCTTGTCTTC ACGCAAGGTTATAGGGACTTGCTGGGTTCTTCGCTTATTTTGCCTCAAAGATAGTCCTTGTCTTC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs557706750 Functional Loss SNV dbSNP153 33..33 33 - - - 20038 RMVar_ID_20038 Human_SNP_ID_45144195 A-to-I Human chr1 - 197647908 197647908 197647908 AGTTTCGCTCTTGTTGCCCAGGTTGGAAAACAATGGCGTGATCTCAGCTCAGTGCAAACTCTGCC AGTTTCGCTCTTGTTGCCCAGGTTGGAAAACAGTGGCGTGATCTCAGCTCAGTGCAAACTCTGCC T C DENND1B Ensembl:ENSG00000213047 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1191297073 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58827,RMVar_hsa_circ_102729,RMVar_hsa_circ_364043,RMVar_hsa_circ_138628,RMVar_hsa_circ_101378,RMVar_hsa_circ_67613,RMVar_hsa_circ_43116,RMVar_hsa_circ_138630,RMVar_hsa_circ_366278,RMVar_hsa_circ_74323,RMVar_hsa_circ_318169,RMVar_hsa_circ_72097,RMVar_hsa_circ_350751,RMVar_hsa_circ_301221,RMVar_hsa_circ_305222,RMVar_hsa_circ_301006,RMVar_hsa_circ_286428,RMVar_hsa_circ_138639,RMVar_hsa_circ_138640,RMVar_hsa_circ_138641,RMVar_hsa_circ_302311,RMVar_hsa_circ_351048,RMVar_hsa_circ_364019,RMVar_hsa_circ_350680,RMVar_hsa_circ_282010,RMVar_hsa_circ_138656,RMVar_hsa_circ_46153,RMVar_hsa_circ_70573,RMVar_hsa_circ_138643,RMVar_hsa_circ_367383,RMVar_hsa_circ_138642,RMVar_hsa_circ_363159,RMVar_hsa_circ_330227,RMVar_hsa_circ_301912,RMVar_hsa_circ_59995,RMVar_hsa_circ_138647,RMVar_hsa_circ_2850,RMVar_hsa_circ_138648,RMVar_hsa_circ_343306,RMVar_hsa_circ_370840,RMVar_hsa_circ_326641,RMVar_hsa_circ_278251,RMVar_hsa_circ_68917,RMVar_hsa_circ_75870,RMVar_hsa_circ_293351,RMVar_hsa_circ_138652,RMVar_hsa_circ_138653,RMVar_hsa_circ_318853,RMVar_hsa_circ_338384,RMVar_hsa_circ_293861,RMVar_hsa_circ_273524,RMVar_hsa_circ_270341,RMVar_hsa_circ_138658,RMVar_hsa_circ_138660,RMVar_hsa_circ_138659,RMVar_hsa_circ_138657,RMVar_hsa_circ_138654,RMVar_hsa_circ_138655,RMVar_hsa_circ_40643 20039 RMVar_ID_20039 Human_SNP_ID_45170777 A-to-I Human chr1 - 197763156 197763156 197763156 CAGGCGTATGTCACCATGTCTGGCTAATTTTTACATTTTTTGTACAGATGGGGTCTCACTCTGTT CAGGCGTATGTCACCATGTCTGGCTAATTTTTTCATTTTTTGTACAGATGGGGTCTCACTCTGTT T A DENND1B Ensembl:ENSG00000213047 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1211709434 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72097,RMVar_hsa_circ_301221,RMVar_hsa_circ_138641,RMVar_hsa_circ_351048,RMVar_hsa_circ_46153,RMVar_hsa_circ_330227,RMVar_hsa_circ_138648,RMVar_hsa_circ_75870,RMVar_hsa_circ_338384,RMVar_hsa_circ_7060,RMVar_hsa_circ_138654,RMVar_hsa_circ_138655,RMVar_hsa_circ_362637,RMVar_hsa_circ_349893 20040 RMVar_ID_20040 Human_SNP_ID_45269342 A-to-I Human chr1 + 198171040 198171040 198171040 TCCTCACCTTAGCCTCCTGAAGTGTTGAGATTACAGGCATGAGCCACTGCACCTGGCCAAAACAT TCCTCACCTTAGCCTCCTGAAGTGTTGAGATTGCAGGCATGAGCCACTGCACCTGGCCAAAACAT A G NEK7 Ensembl:ENSG00000151414 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968798488 Functional Loss SNV dbSNP153 33..33 33 - - - 20041 RMVar_ID_20041 Human_SNP_ID_45292149 A-to-I Human chr1 + 198265936 198265936 198265936 CTATATATTATGTTACTTAACCATCATAATAAAACTATATGACAGGTATTACTGACCCAATTTTA CTATATATTATGTTACTTAACCATCATAATAACACTATATGACAGGTATTACTGACCCAATTTTA A C NEK7 Ensembl:ENSG00000151414 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1479504912 Functional Loss SNV dbSNP153 33..33 33 - - - 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 20042 RMVar_ID_20042 Human_SNP_ID_45292150 A-to-I Human chr1 + 198265940 198265940 198265940 ATATTATGTTACTTAACCATCATAATAAAACTATATGACAGGTATTACTGACCCAATTTTATTTA ATATTATGTTACTTAACCATCATAATAAAACTGTATGACAGGTATTACTGACCCAATTTTATTTA A G NEK7 Ensembl:ENSG00000151414 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1197509527 Functional Loss SNV dbSNP153 33..33 33 - - - 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 20043 RMVar_ID_20043 Human_SNP_ID_45292152 A-to-I Human chr1 + 198265951 198265951 198265951 CTTAACCATCATAATAAAACTATATGACAGGTATTACTGACCCAATTTTATTTATATGGTCCTTC CTTAACCATCATAATAAAACTATATGACAGGTGTTACTGACCCAATTTTATTTATATGGTCCTTC A G NEK7 Ensembl:ENSG00000151414 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs981816201 Functional Loss SNV dbSNP153 33..33 33 - - - 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 20044 RMVar_ID_20044 Human_SNP_ID_45292333 A-to-I Human chr1 + 198266737 198266737 198266737 GTTAAGTAATATAATATATAGTATGTTTATATATATACTTTTTAAAGACATATGTACAAATGTAT GTTAAGTAATATAATATATAGTATGTTTATATGTATACTTTTTAAAGACATATGTACAAATGTAT A G NEK7 Ensembl:ENSG00000151414 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs892292752 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23354596 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 20045 RMVar_ID_20045 Human_SNP_ID_45292337 A-to-I Human chr1 + 198266762 198266762 198266762 TTTATATATATACTTTTTAAAGACATATGTACAAATGTATGTGCACATACCCATCCATCTGTGCC TTTATATATATACTTTTTAAAGACATATGTACTAATGTATGTGCACATACCCATCCATCTGTGCC A T NEK7 Ensembl:ENSG00000151414 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432682649 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23354596 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 20046 RMVar_ID_20046 Human_SNP_ID_45292338 A-to-I Human chr1 + 198266768 198266768 198266768 TATATACTTTTTAAAGACATATGTACAAATGTATGTGCACATACCCATCCATCTGTGCCTGTATG TATATACTTTTTAAAGACATATGTACAAATGTGTGTGCACATACCCATCCATCTGTGCCTGTATG A G NEK7 Ensembl:ENSG00000151414 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs926783457 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18559424,Human_RBP_ID_23354596 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 20047 RMVar_ID_20047 Human_SNP_ID_45295750 A-to-I Human chr1 + 198281889 198281884 198281890 TAGTCTGTCTTCTGTAGCAAATAAAGTTGTATAGGTGGCCACATTTCCAATTAGTTTTCAGAACC TAGTCTGTCTTCTGTAGCAAATAAAGTT______GTGGCCACATTTCCAATTAGTTTTCAGAACC TGTATAG T NEK7 Ensembl:ENSG00000151414 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1178035539 Functional Loss DEL dbSNP153 29..34 33 - - - Human_RBP_ID_2114348 RMVar_hsa_circ_138669,RMVar_hsa_circ_292860,RMVar_hsa_circ_303608,RMVar_hsa_circ_138670,RMVar_hsa_circ_345173,RMVar_hsa_circ_138678,RMVar_hsa_circ_281371,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_333223 20048 RMVar_ID_20048 Human_SNP_ID_45836209 A-to-I Human chr1 - 200563673 200563673 200563673 AAATTAATGGCCGAGTACAGTGGCTCATGCCTATAATACTAGGACTTTGGGAGGCTGAGGCAGGA AAATTAATGGCCGAGTACAGTGGCTCATGCCTGTAATACTAGGACTTTGGGAGGCTGAGGCAGGA T C KIF14 Ensembl:ENSG00000118193 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053205503 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10557,RMVar_hsa_circ_116910,RMVar_hsa_circ_138695,RMVar_hsa_circ_336157,RMVar_hsa_circ_27039,RMVar_hsa_circ_55321 20049 RMVar_ID_20049 Human_SNP_ID_45840804 A-to-I Human chr1 - 200581934 200581934 200581934 AAAACCTCCTCTCTACAAAATATAAGAAAGTTAGCTGGGTGTGGTGGCATGCACCTGTAGTTCCA AAAACCTCCTCTCTACAAAATATAAGAAAGTTGGCTGGGTGTGGTGGCATGCACCTGTAGTTCCA T C KIF14 Ensembl:ENSG00000118193 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs943245030 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2305,RMVar_hsa_circ_116910,RMVar_hsa_circ_138695,RMVar_hsa_circ_336157,RMVar_hsa_circ_59864,RMVar_hsa_circ_97656,RMVar_hsa_circ_378925,RMVar_hsa_circ_371805,RMVar_hsa_circ_353952,RMVar_hsa_circ_269154,RMVar_hsa_circ_70023,RMVar_hsa_circ_65484,RMVar_hsa_circ_138699,RMVar_hsa_circ_138701,RMVar_hsa_circ_57236,RMVar_hsa_circ_138700,RMVar_hsa_circ_309148,RMVar_hsa_circ_347954,RMVar_hsa_circ_358918,RMVar_hsa_circ_368421,RMVar_hsa_circ_348071,RMVar_hsa_circ_25432,RMVar_hsa_circ_8181,RMVar_hsa_circ_117336,RMVar_hsa_circ_138703,RMVar_hsa_circ_69392,RMVar_hsa_circ_138706,RMVar_hsa_circ_344415,RMVar_hsa_circ_138705,RMVar_hsa_circ_359322,RMVar_hsa_circ_373879,RMVar_hsa_circ_349602,RMVar_hsa_circ_72166,RMVar_hsa_circ_291780,RMVar_hsa_circ_31794,RMVar_hsa_circ_302101,RMVar_hsa_circ_338914,RMVar_hsa_circ_363796,RMVar_hsa_circ_325856,RMVar_hsa_circ_271724,RMVar_hsa_circ_138708,RMVar_hsa_circ_138710,RMVar_hsa_circ_3576,RMVar_hsa_circ_138711,RMVar_hsa_circ_138709,RMVar_hsa_circ_138707 20050 RMVar_ID_20050 Human_SNP_ID_45855598 A-to-I Human chr1 - 200644747 200644747 200644747 GAATTTACAGGTGTTTGCCACCATGCCTGGCTAATTTTTGTGTTTTTAGTAGAGACAGGATTTTG GAATTTACAGGTGTTTGCCACCATGCCTGGCTTATTTTTGTGTTTTTAGTAGAGACAGGATTTTG T A DDX59 Ensembl:ENSG00000118197 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1218342409 Functional Loss SNV dbSNP153 33..33 33 - - - 20051 RMVar_ID_20051 Human_SNP_ID_45855604 A-to-I Human chr1 - 200644780 200644780 200644780 GCGATTCTTTTGCCTCAGCCTCCCAAGTAGCTAGAATTTACAGGTGTTTGCCACCATGCCTGGCT GCGATTCTTTTGCCTCAGCCTCCCAAGTAGCTCGAATTTACAGGTGTTTGCCACCATGCCTGGCT T G DDX59 Ensembl:ENSG00000118197 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1293439748 Functional Loss SNV dbSNP153 33..33 33 - - - 20052 RMVar_ID_20052 Human_SNP_ID_45856382 A-to-I Human chr1 - 200648148 200648148 200648148 ATGGTGGCAGGCGCTTGTAGTCCCAACTACTCAGGAGGCTGAGGCAGGAAAATCGCTTGAACTCG ATGGTGGCAGGCGCTTGTAGTCCCAACTACTCCGGAGGCTGAGGCAGGAAAATCGCTTGAACTCG T G DDX59 Ensembl:ENSG00000118197 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1288902087 Functional Loss SNV dbSNP153 33..33 33 - - - 20053 RMVar_ID_20053 Human_SNP_ID_45856436 A-to-I Human chr1 - 200648326 200648326 200648326 AGAAAGCAGTATCGGCCAGGACAGTGGCTCACACCTGTAATCCCAGCACTTTGGAAGGCCATCGC AGAAAGCAGTATCGGCCAGGACAGTGGCTCACGCCTGTAATCCCAGCACTTTGGAAGGCCATCGC T C DDX59 Ensembl:ENSG00000118197 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs990177511 Functional Loss SNV dbSNP153 33..33 33 - - - 20054 RMVar_ID_20054 Human_SNP_ID_45856780 A-to-I Human chr1 - 200649620 200649620 200649620 TGTTTTGTGTTTTTTTTTTTTTTTGTGACGGAATCTCACTCTGTTGCCCAGGCTGGAGTGCTATG TGTTTTGTGTTTTTTTTTTTTTTTGTGACGGAGTCTCACTCTGTTGCCCAGGCTGGAGTGCTATG T C DDX59 Ensembl:ENSG00000118197 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1428550589 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_138724,RMVar_hsa_circ_279861,RMVar_hsa_circ_334591,RMVar_hsa_circ_321380,RMVar_hsa_circ_138725 20055 RMVar_ID_20055 Human_SNP_ID_45856781 A-to-I Human chr1 - 200649620 200649620 200649620 TGTTTTGTGTTTTTTTTTTTTTTTGTGACGGAATCTCACTCTGTTGCCCAGGCTGGAGTGCTATG TGTTTTGTGTTTTTTTTTTTTTTTGTGACGGACTCTCACTCTGTTGCCCAGGCTGGAGTGCTATG T G DDX59 Ensembl:ENSG00000118197 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1428550589 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_138724,RMVar_hsa_circ_279861,RMVar_hsa_circ_334591,RMVar_hsa_circ_321380,RMVar_hsa_circ_138725 20056 RMVar_ID_20056 Human_SNP_ID_45856888 A-to-I Human chr1 - 200649928 200649928 200649928 TGAGGCAGGAGAATGGTGTGAATCTGGGAGGCAGGGCTTGTAGTGAGCTGAGATTGCGCCACTGC TGAGGCAGGAGAATGGTGTGAATCTGGGAGGCGGGGCTTGTAGTGAGCTGAGATTGCGCCACTGC T C DDX59 Ensembl:ENSG00000118197 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1409758368 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_138724,RMVar_hsa_circ_279861,RMVar_hsa_circ_334591,RMVar_hsa_circ_321380,RMVar_hsa_circ_138725 20057 RMVar_ID_20057 Human_SNP_ID_45857548 A-to-I Human chr1 - 200652572 200652572 200652572 ACATGTTAGAAAGTGGGGGTGGAGCCTGGGCAACATAGCAAAACCCCATCTCTACTAAAAATACA ACATGTTAGAAAGTGGGGGTGGAGCCTGGGCAGCATAGCAAAACCCCATCTCTACTAAAAATACA T C DDX59 Ensembl:ENSG00000118197 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs767210622 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5738132 RMVar_hsa_circ_138724,RMVar_hsa_circ_334591,RMVar_hsa_circ_321380,RMVar_hsa_circ_138725,RMVar_hsa_circ_364449 20058 RMVar_ID_20058 Human_SNP_ID_45857653 A-to-I Human chr1 - 200652966 200652966 200652966 TCAGGAGAGGAGATGTCTGGGTGCAGGGGCCCACGCCTGTAATCCCAGCACTTTGGGAGGTCAAG TCAGGAGAGGAGATGTCTGGGTGCAGGGGCCCGCGCCTGTAATCCCAGCACTTTGGGAGGTCAAG T C DDX59 Ensembl:ENSG00000118197 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1229115848 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_138724,RMVar_hsa_circ_334591,RMVar_hsa_circ_321380,RMVar_hsa_circ_138725,RMVar_hsa_circ_364449 20059 RMVar_ID_20059 Human_SNP_ID_45887303 A-to-I Human chr1 + 200775457 200775457 200775457 GACAATGAGTTGATCTGGTTTATTTTTTTTTCAGAATCATTAAATGCCATAATAATAATTTTGGT GACAATGAGTTGATCTGGTTTATTTTTTTTTCGGAATCATTAAATGCCATAATAATAATTTTGGT A G CAMSAP2 Ensembl:ENSG00000118200 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs542444370 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88719,RMVar_hsa_circ_127526,RMVar_hsa_circ_102969,RMVar_hsa_circ_138729,RMVar_hsa_circ_138730,RMVar_hsa_circ_289079,RMVar_hsa_circ_309414,RMVar_hsa_circ_368222,RMVar_hsa_circ_372278,RMVar_hsa_circ_309942,RMVar_hsa_circ_305179,RMVar_hsa_circ_276931,RMVar_hsa_circ_89202,RMVar_hsa_circ_138732,RMVar_hsa_circ_138734,RMVar_hsa_circ_138736,RMVar_hsa_circ_138738,RMVar_hsa_circ_138737,RMVar_hsa_circ_138735,RMVar_hsa_circ_138733 20060 RMVar_ID_20060 Human_SNP_ID_45942932 A-to-I Human chr1 - 201001556 201001556 201001556 GGCAACATAGGGACGCCTAGTCTCTACAAAAAATACAAAAATTAGCCAGATGTGGTGGCACATGC GGCAACATAGGGACGCCTAGTCTCTACAAAAAGTACAAAAATTAGCCAGATGTGGTGGCACATGC T C KIF21B Ensembl:ENSG00000116852 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1305106388 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_138769,RMVar_hsa_circ_374005,RMVar_hsa_circ_67853 20061 RMVar_ID_20061 Human_SNP_ID_46066326 A-to-I Human chr1 - 201460894 201460894 201460894 TGGAGTTTCATCATTTTGAACTCCTGAGCTCAAGCGATTCACCTGCCTCAGCCTTCCAAAGTATT TGGAGTTTCATCATTTTGAACTCCTGAGCTCAGGCGATTCACCTGCCTCAGCCTTCCAAAGTATT T C lnc-PHLDA3-2 RNACentral:URS00008BB9C1 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1341407707 Functional Loss SNV dbSNP153 33..33 33 - - - 20062 RMVar_ID_20062 Human_SNP_ID_46067018 A-to-I Human chr1 - 201463542 201463542 201463542 ACTGTAATCCCAGCTACTCGGAAGGCTGAGGAAGGAGAATCGATTGAACTCTGGAGGTGGAGGTT ACTGTAATCCCAGCTACTCGGAAGGCTGAGGAGGGAGAATCGATTGAACTCTGGAGGTGGAGGTT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1299614479 Functional Loss SNV dbSNP153 33..33 33 - - - 20063 RMVar_ID_20063 Human_SNP_ID_46079699 A-to-I Human chr1 + 201515331 201515331 201515331 CACCTTGTCTGCTGCCTAGACAGAGCCGATTTATCAAGACAGGAGAATAGCAATGGAGAAAGAGT CACCTTGTCTGCTGCCTAGACAGAGCCGATTTGTCAAGACAGGAGAATAGCAATGGAGAAAGAGT A G AC096677.1 Ensembl:ENSG00000224536 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs116343104 Functional Loss SNV dbSNP153 33..33 33 - - - 20064 RMVar_ID_20064 Human_SNP_ID_46079744 A-to-I Human chr1 + 201515514 201515514 201515514 GTGCTAATTGCTCAGGTTGGAGATGGAATCATAGAGGGTCGAAGTGAGTTTTTTGTGCTATTTTC GTGCTAATTGCTCAGGTTGGAGATGGAATCATGGAGGGTCGAAGTGAGTTTTTTGTGCTATTTTC A G AC096677.1 Ensembl:ENSG00000224536 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs370854214 Functional Loss SNV dbSNP153 33..33 33 - - - 20065 RMVar_ID_20065 Human_SNP_ID_46079748 A-to-I Human chr1 + 201515528 201515528 201515528 GGTTGGAGATGGAATCATAGAGGGTCGAAGTGAGTTTTTTGTGCTATTTTCTGTTCCTGGGTGGG GGTTGGAGATGGAATCATAGAGGGTCGAAGTGGGTTTTTTGTGCTATTTTCTGTTCCTGGGTGGG A G AC096677.1 Ensembl:ENSG00000224536 lincRNA intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs976335670 Functional Loss SNV dbSNP153 33..33 33 - - - 20066 RMVar_ID_20066 Human_SNP_ID_46079754 A-to-I Human chr1 + 201515568 201515568 201515568 GTGCTATTTTCTGTTCCTGGGTGGGATGGCAGAACTGGTTGAGCCAGATTACAGTTCTGGGTTGT GTGCTATTTTCTGTTCCTGGGTGGGATGGCAGCACTGGTTGAGCCAGATTACAGTTCTGGGTTGT A C AC096677.1 Ensembl:ENSG00000224536 lincRNA intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs1181837144 Functional Loss SNV dbSNP153 33..33 33 - - - 20067 RMVar_ID_20067 Human_SNP_ID_46079809 A-to-I Human chr1 + 201515851 201515851 201515851 GAAAGGTCTATTATTAATTTTGTTTTAGAGTCAAATCATGAACTGAATTCCTTCAGGGCAAAGTT GAAAGGTCTATTATTAATTTTGTTTTAGAGTCGAATCATGAACTGAATTCCTTCAGGGCAAAGTT A G AC096677.1 Ensembl:ENSG00000224536 lincRNA intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs907500484 Functional Loss SNV dbSNP153 33..33 33 - - - 20068 RMVar_ID_20068 Human_SNP_ID_46080227 A-to-I Human chr1 + 201517328 201517328 201517328 GAGGAATTCAGCTTATAACTTAACTTTGAAGCAAAGATGAAAACAGCCTTTTCCCTTAACACAGC GAGGAATTCAGCTTATAACTTAACTTTGAAGCCAAGATGAAAACAGCCTTTTCCCTTAACACAGC A C AC096677.1 Ensembl:ENSG00000224536 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1317127401 Functional Loss SNV dbSNP153 33..33 33 - - - 20069 RMVar_ID_20069 Human_SNP_ID_46080337 A-to-I Human chr1 + 201517774 201517774 201517774 TTTGAACCTCCCCCATTGCTCCGAAAGATAACATCACTATTGTAAAACCTAAGATCAGTGCTCCA TTTGAACCTCCCCCATTGCTCCGAAAGATAACCTCACTATTGTAAAACCTAAGATCAGTGCTCCA A C AC096677.1 Ensembl:ENSG00000224536 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1233429136 Functional Loss SNV dbSNP153 33..33 33 - - - 20070 RMVar_ID_20070 Human_SNP_ID_46080338 A-to-I Human chr1 + 201517777 201517777 201517777 GAACCTCCCCCATTGCTCCGAAAGATAACATCACTATTGTAAAACCTAAGATCAGTGCTCCAGAC GAACCTCCCCCATTGCTCCGAAAGATAACATCTCTATTGTAAAACCTAAGATCAGTGCTCCAGAC A T AC096677.1 Ensembl:ENSG00000224536 lincRNA intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1276043049 Functional Loss SNV dbSNP153 33..33 33 - - - 20071 RMVar_ID_20071 Human_SNP_ID_46080340 A-to-I Human chr1 + 201517792 201517792 201517792 CTCCGAAAGATAACATCACTATTGTAAAACCTAAGATCAGTGCTCCAGACATTTTTCACACTGCA CTCCGAAAGATAACATCACTATTGTAAAACCTGAGATCAGTGCTCCAGACATTTTTCACACTGCA A G AC096677.1 Ensembl:ENSG00000224536 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1557982140 Functional Loss SNV dbSNP153 33..33 33 - - - 20072 RMVar_ID_20072 Human_SNP_ID_46080344 A-to-I Human chr1 + 201517806 201517806 201517806 ATCACTATTGTAAAACCTAAGATCAGTGCTCCAGACATTTTTCACACTGCATTCTGATGCACCAG ATCACTATTGTAAAACCTAAGATCAGTGCTCCCGACATTTTTCACACTGCATTCTGATGCACCAG A C AC096677.1 Ensembl:ENSG00000224536 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749687900 Functional Loss SNV dbSNP153 33..33 33 - - - 20073 RMVar_ID_20073 Human_SNP_ID_46080350 A-to-I Human chr1 + 201517853 201517853 201517853 TGCATTCTGATGCACCAGCTGGCCCCACCCAGATCGGTAATCTGGCTCAACCAGTTCTGGGATCT TGCATTCTGATGCACCAGCTGGCCCCACCCAGGTCGGTAATCTGGCTCAACCAGTTCTGGGATCT A G AC096677.1 Ensembl:ENSG00000224536 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005537032 Functional Loss SNV dbSNP153 33..33 33 - - - 20074 RMVar_ID_20074 Human_SNP_ID_46080376 A-to-I Human chr1 + 201517932 201517932 201517932 GGACAGGAAGAAAAATCCCACTTTGACCCCCTATGATTTCATCGCTGACCCAGCCAATCAGCATT GGACAGGAAGAAAAATCCCACTTTGACCCCCTGTGATTTCATCGCTGACCCAGCCAATCAGCATT A G AC096677.1 Ensembl:ENSG00000224536 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs775033322 Functional Loss SNV dbSNP153 33..33 33 - - - 20075 RMVar_ID_20075 Human_SNP_ID_46080397 A-to-I Human chr1 + 201518018 201518018 201518018 ACACCAAATTATCCTTAAAAATTCCAGTCTCCAAATTTTCCAGGAGACTGGTTTGAGTAATAATA ACACCAAATTATCCTTAAAAATTCCAGTCTCCCAATTTTCCAGGAGACTGGTTTGAGTAATAATA A C AC096677.1 Ensembl:ENSG00000224536 lincRNA intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1467531423 Functional Loss SNV dbSNP153 33..33 33 - - - 20076 RMVar_ID_20076 Human_SNP_ID_46080410 A-to-I Human chr1 + 201518119 201518119 201518119 TAAACTCTTCATTGCAATTCCCCTGTCTTGATAAATCTGCTCTGTCTGCGTATCAGGCAAGGAGA TAAACTCTTCATTGCAATTCCCCTGTCTTGATGAATCTGCTCTGTCTGCGTATCAGGCAAGGAGA A G AC096677.1 Ensembl:ENSG00000224536 lincRNA intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1320952589 Functional Loss SNV dbSNP153 33..33 33 - - - 20077 RMVar_ID_20077 Human_SNP_ID_46080497 A-to-I Human chr1 + 201518386 201518386 201518386 CTACCCCCTTGCCCAGTAGCTGTGACTACTACAGGTGCAGGCCACCAAGTCTGGCTAATTTTTAT CTACCCCCTTGCCCAGTAGCTGTGACTACTACGGGTGCAGGCCACCAAGTCTGGCTAATTTTTAT A G AC096677.1 Ensembl:ENSG00000224536 lincRNA intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs1270034385 Functional Loss SNV dbSNP153 33..33 33 - - - 20078 RMVar_ID_20078 Human_SNP_ID_46080585 A-to-I Human chr1 + 201518809 201518809 201518809 CTTTTTTTGTTGTTTTTTTGAGACAGGGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGATGCA CTTTTTTTGTTGTTTTTTTGAGACAGGGTCTCGCTCTGTCACCCAGGCTGGAGTGCAGTGATGCA A G RPS10P7,AC096677.1 Ensembl:ENSG00000223396,Ensembl:ENSG00000224536 Pseudogene,lincRNA exon,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1467981535 Functional Loss SNV dbSNP153 33..33 33 - - - 20079 RMVar_ID_20079 Human_SNP_ID_46080606 A-to-I Human chr1 + 201518911 201518911 201518911 GCAATCCTCCTGCCTCAGCCTCCTGAGTAGCTAGGACTACAGGTGTATGCCACCATGCCTGGCTA GCAATCCTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGTGTATGCCACCATGCCTGGCTA A G RPS10P7,AC096677.1 Ensembl:ENSG00000223396,Ensembl:ENSG00000224536 Pseudogene,lincRNA exon,intron GSE38233;GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1164042533 Functional Loss SNV dbSNP153 33..33 33 - - - 20080 RMVar_ID_20080 Human_SNP_ID_46080777 A-to-I Human chr1 + 201519636 201519636 201519636 TAGTGGTTGACTCGCCGCTCGCAATGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGC TAGTGGTTGACTCGCCGCTCGCAATGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGC A G RPS10P7,AC096677.1 Ensembl:ENSG00000223396,Ensembl:ENSG00000224536 Pseudogene,lincRNA exon,intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1216734255 Functional Loss SNV dbSNP153 33..33 33 - - - 20081 RMVar_ID_20081 Human_SNP_ID_46081181 A-to-I Human chr1 + 201521155 201521155 201521155 CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTATAGACACACACCACCACACCCGCTAATTTTTG CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTGTAGACACACACCACCACACCCGCTAATTTTTG A G RPS10P7,AC096677.1 Ensembl:ENSG00000223396,Ensembl:ENSG00000224536 Pseudogene,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1310505497 Functional Loss SNV dbSNP153 33..33 33 - - - 20082 RMVar_ID_20082 Human_SNP_ID_46081272 A-to-I Human chr1 + 201521501 201521501 201521501 GAGAGTGCAGCGGTGTGATCATAGCTCACTGTAACTTGTAACTTCTGGACTCAAGCAATCCTCCC GAGAGTGCAGCGGTGTGATCATAGCTCACTGTGACTTGTAACTTCTGGACTCAAGCAATCCTCCC A G RPS10P7,AC096677.1 Ensembl:ENSG00000223396,Ensembl:ENSG00000224536 Pseudogene,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1226027855 Functional Loss SNV dbSNP153 33..33 33 - - - 20083 RMVar_ID_20083 Human_SNP_ID_46082538 A-to-I Human chr1 + 201526735 201526735 201526735 GAGGTCAGGAGATCAAGACCATCCTGGCTAACAAGGTGAAACCCCGTCTGTACTGAAGATACAAA GAGGTCAGGAGATCAAGACCATCCTGGCTAACGAGGTGAAACCCCGTCTGTACTGAAGATACAAA A G RPS10P7,AC096677.1 Ensembl:ENSG00000223396,Ensembl:ENSG00000224536 Pseudogene,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1401135427 Functional Loss SNV dbSNP153 33..33 33 - - - 20084 RMVar_ID_20084 Human_SNP_ID_46083742 A-to-I Human chr1 + 201531480 201531480 201531480 CAGCCCAGAGTCTCCGGAACGAAGGTCTCCACAGCCAAAGCCACGCAAGAGGCTCTCCTGCTCTC CAGCCCAGAGTCTCCGGAACGAAGGTCTCCACGGCCAAAGCCACGCAAGAGGCTCTCCTGCTCTC A G RPS10P7,AC096677.1 Ensembl:ENSG00000223396,Ensembl:ENSG00000224536 Pseudogene,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4915536 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_1740,GWAS_ID_1741,GWAS_ID_1742,GWAS_ID_1743,GWAS_ID_1744 20085 RMVar_ID_20085 Human_SNP_ID_46084186 A-to-I Human chr1 + 201533515 201533515 201533515 CCCTCCACCTCCCAGGCTCAAGCCATCCTCCTATCTCAGCCTCCTGAGTAGTTGAGACAACAGGC CCCTCCACCTCCCAGGCTCAAGCCATCCTCCTGTCTCAGCCTCCTGAGTAGTTGAGACAACAGGC A G RPS10P7,AC096677.1 Ensembl:ENSG00000223396,Ensembl:ENSG00000224536 Pseudogene,lincRNA intron,exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs893657515 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5091627 Human_Splice_Rec_172998 20086 RMVar_ID_20086 Human_SNP_ID_46106816 A-to-I Human chr1 - 201627984 201627984 201627984 CAGGCTCAAGCTACCACGCCTAGCTGATTTTCATATTTTTTGTAGAGATGGGGTTTTGCCATGTC CAGGCTCAAGCTACCACGCCTAGCTGATTTTCGTATTTTTTGTAGAGATGGGGTTTTGCCATGTC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215054888 Functional Loss SNV dbSNP153 33..33 33 - - - 20087 RMVar_ID_20087 Human_SNP_ID_46106817 A-to-I Human chr1 - 201627984 201627984 201627984 CAGGCTCAAGCTACCACGCCTAGCTGATTTTCATATTTTTTGTAGAGATGGGGTTTTGCCATGTC CAGGCTCAAGCTACCACGCCTAGCTGATTTTCCTATTTTTTGTAGAGATGGGGTTTTGCCATGTC T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215054888 Functional Loss SNV dbSNP153 33..33 33 - - - 20088 RMVar_ID_20088 Human_SNP_ID_46148701 A-to-I Human chr1 + 201806185 201806185 201806185 TTTTGTATTTTTAGTAGAGACGCGGTTTCACCATCTCGGCCAGGCTAGTCTCAAACTCCTGACCT TTTTGTATTTTTAGTAGAGACGCGGTTTCACCCTCTCGGCCAGGCTAGTCTCAAACTCCTGACCT A C NAV1 Ensembl:ENSG00000134369 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1164612251 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_138815,RMVar_hsa_circ_80748,RMVar_hsa_circ_95589,RMVar_hsa_circ_138817,RMVar_hsa_circ_80508,RMVar_hsa_circ_116046,RMVar_hsa_circ_138819,RMVar_hsa_circ_138821,RMVar_hsa_circ_10501,RMVar_hsa_circ_82393,RMVar_hsa_circ_108040,RMVar_hsa_circ_138823,RMVar_hsa_circ_138824,RMVar_hsa_circ_91187,RMVar_hsa_circ_79881,RMVar_hsa_circ_138826,RMVar_hsa_circ_138827 20089 RMVar_ID_20089 Human_SNP_ID_46148702 A-to-I Human chr1 + 201806185 201806185 201806185 TTTTGTATTTTTAGTAGAGACGCGGTTTCACCATCTCGGCCAGGCTAGTCTCAAACTCCTGACCT TTTTGTATTTTTAGTAGAGACGCGGTTTCACCGTCTCGGCCAGGCTAGTCTCAAACTCCTGACCT A G NAV1 Ensembl:ENSG00000134369 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1164612251 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_138815,RMVar_hsa_circ_80748,RMVar_hsa_circ_95589,RMVar_hsa_circ_138817,RMVar_hsa_circ_80508,RMVar_hsa_circ_116046,RMVar_hsa_circ_138819,RMVar_hsa_circ_138821,RMVar_hsa_circ_10501,RMVar_hsa_circ_82393,RMVar_hsa_circ_108040,RMVar_hsa_circ_138823,RMVar_hsa_circ_138824,RMVar_hsa_circ_91187,RMVar_hsa_circ_79881,RMVar_hsa_circ_138826,RMVar_hsa_circ_138827 20090 RMVar_ID_20090 Human_SNP_ID_46156360 A-to-I Human chr1 + 201839286 201839286 201839286 TCACCCAGGCTGGAGTGCAGTGGCTCAGTCTCAGCTCACTGCAACATCTGCCTCCCAGGCCCAAG TCACCCAGGCTGGAGTGCAGTGGCTCAGTCTCGGCTCACTGCAACATCTGCCTCCCAGGCCCAAG A G IPO9 Ensembl:ENSG00000198700 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1315788273 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84187,RMVar_hsa_circ_323536,RMVar_hsa_circ_138839 20091 RMVar_ID_20091 Human_SNP_ID_46167507 A-to-I Human chr1 - 201883318 201883318 201883318 CTCTCCCCTTCTTCCTCCGGGACCCTGGGCCTAATTGCAGTTCACTAGAGCTTTCACCATAGGGT CTCTCCCCTTCTTCCTCCGGGACCCTGGGCCTCATTGCAGTTCACTAGAGCTTTCACCATAGGGT T G - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs533084605 Functional Loss SNV dbSNP153 33..33 33 - - - 20092 RMVar_ID_20092 Human_SNP_ID_46187758 A-to-I Human chr1 + 201959343 201959343 201959343 GCACCACTGTACTCCAGGCGGGGTGACAGAGCAAGACTCTGTCTCTAAAAAATAAAATAAAAGGG GCACCACTGTACTCCAGGCGGGGTGACAGAGCCAGACTCTGTCTCTAAAAAATAAAATAAAAGGG A C TIMM17A Ensembl:ENSG00000134375 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1262868860 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_367177,RMVar_hsa_circ_18961 20093 RMVar_ID_20093 Human_SNP_ID_46187867 A-to-I Human chr1 + 201959725 201959725 201959725 GGCCGGGCGCGGTGGCTCACGACTGTAATCCCAGCACTTTCGGAGGCCGAGGCAGGTGGATCACA GGCCGGGCGCGGTGGCTCACGACTGTAATCCCGGCACTTTCGGAGGCCGAGGCAGGTGGATCACA A G TIMM17A Ensembl:ENSG00000134375 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1318310037 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17558060 RMVar_hsa_circ_367177,RMVar_hsa_circ_18961 20094 RMVar_ID_20094 Human_SNP_ID_46187944 A-to-I Human chr1 + 201959966 201959966 201959966 AACTTGGCAGTGAGCCCAGATCACACCACTGTACTCCAGCCAGGGTGACAGCGAGACTCTGTCTC AACTTGGCAGTGAGCCCAGATCACACCACTGTTCTCCAGCCAGGGTGACAGCGAGACTCTGTCTC A T TIMM17A Ensembl:ENSG00000134375 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1021358633 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9557383,Human_RBP_ID_10726233,Human_RBP_ID_24756088 RMVar_hsa_circ_367177,RMVar_hsa_circ_18961 20095 RMVar_ID_20095 Human_SNP_ID_46187985 A-to-I Human chr1 + 201960138 201960138 201960138 TAGTAATGTGTCGGCCGGGCACAGTGGCTCACACCTGTAATCCCAGCACTTCGGGAGGCTGAGGC TAGTAATGTGTCGGCCGGGCACAGTGGCTCACGCCTGTAATCCCAGCACTTCGGGAGGCTGAGGC A G TIMM17A Ensembl:ENSG00000134375 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs886792684 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_367177,RMVar_hsa_circ_18961 20096 RMVar_ID_20096 Human_SNP_ID_46188165 A-to-I Human chr1 + 201960842 201960842 201960842 ACAGTCTTGGCTCACTGCAACCTCCGCCTCCCAGGTTCAAGTGATGCTCCCACCTCAGCCTCCTG ACAGTCTTGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGTGATGCTCCCACCTCAGCCTCCTG A G TIMM17A Ensembl:ENSG00000134375 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1324963836 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_367177,RMVar_hsa_circ_18961 20097 RMVar_ID_20097 Human_SNP_ID_46188206 A-to-I Human chr1 + 201961011 201961011 201961011 ACCTCAGGTGATCCGCCTACCTCAGCCTCCCAAAGTGCTGAGATTACAGGCATGAGCCACCACGC ACCTCAGGTGATCCGCCTACCTCAGCCTCCCACAGTGCTGAGATTACAGGCATGAGCCACCACGC A C TIMM17A Ensembl:ENSG00000134375 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs760618797 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_367177,RMVar_hsa_circ_18961 20098 RMVar_ID_20098 Human_SNP_ID_46188207 A-to-I Human chr1 + 201961011 201961011 201961011 ACCTCAGGTGATCCGCCTACCTCAGCCTCCCAAAGTGCTGAGATTACAGGCATGAGCCACCACGC ACCTCAGGTGATCCGCCTACCTCAGCCTCCCAGAGTGCTGAGATTACAGGCATGAGCCACCACGC A G TIMM17A Ensembl:ENSG00000134375 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs760618797 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_367177,RMVar_hsa_circ_18961 20099 RMVar_ID_20099 Human_SNP_ID_46188211 A-to-I Human chr1 + 201961030 201961030 201961030 CCTCAGCCTCCCAAAGTGCTGAGATTACAGGCATGAGCCACCACGCCCGGACTTAGGTCTTATAT CCTCAGCCTCCCAAAGTGCTGAGATTACAGGCGTGAGCCACCACGCCCGGACTTAGGTCTTATAT A G TIMM17A Ensembl:ENSG00000134375 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1270338919 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_367177,RMVar_hsa_circ_18961 20100 RMVar_ID_20100 Human_SNP_ID_46188256 A-to-I Human chr1 + 201961121 201961121 201961121 GAATTTCGCTCTTGTTGCCCAGGCTAGAGTGCAATGGCGCGGTCTCGGCTCACGTCAACTTCCAT GAATTTCGCTCTTGTTGCCCAGGCTAGAGTGCGATGGCGCGGTCTCGGCTCACGTCAACTTCCAT A G TIMM17A Ensembl:ENSG00000134375 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1392301789 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_367177,RMVar_hsa_circ_18961 20101 RMVar_ID_20101 Human_SNP_ID_46188285 A-to-I Human chr1 + 201961191 201961191 201961191 CGGTTCAAGCGATTGTCCATCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCGCATGCCGCCACT CGGTTCAAGCGATTGTCCATCCTCAGCCTCCCTAGTAGCTGGGATTACAGGCGCATGCCGCCACT A T TIMM17A Ensembl:ENSG00000134375 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs373597516 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_367177,RMVar_hsa_circ_18961 20102 RMVar_ID_20102 Human_SNP_ID_46188301 A-to-I Human chr1 + 201961264 201961264 201961264 AGTTTTTTGTATTTTAGTGGAGATGGGGTTTCACCATGTTGCCCAGGCTGGTCTCGAACTCTTGA AGTTTTTTGTATTTTAGTGGAGATGGGGTTTCTCCATGTTGCCCAGGCTGGTCTCGAACTCTTGA A T TIMM17A Ensembl:ENSG00000134375 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1325763035 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_367177,RMVar_hsa_circ_18961 20103 RMVar_ID_20103 Human_SNP_ID_46188311 A-to-I Human chr1 + 201961301 201961301 201961301 GTTGCCCAGGCTGGTCTCGAACTCTTGAGCTCAGGCAGTCCACCCGTCTTGGCCTCCCAAAGTGC GTTGCCCAGGCTGGTCTCGAACTCTTGAGCTCGGGCAGTCCACCCGTCTTGGCCTCCCAAAGTGC A G TIMM17A Ensembl:ENSG00000134375 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1480008257 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10726264 RMVar_hsa_circ_367177,RMVar_hsa_circ_18961 20104 RMVar_ID_20104 Human_SNP_ID_46188653 A-to-I Human chr1 + 201962586 201962586 201962586 GTTGGCCAGGATGCCCTCGATCTTCTGACCTCATGATCCACCCGCCTCGGCCTCCCAAAATGCTG GTTGGCCAGGATGCCCTCGATCTTCTGACCTCCTGATCCACCCGCCTCGGCCTCCCAAAATGCTG A C TIMM17A Ensembl:ENSG00000134375 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs550900636 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_367177,RMVar_hsa_circ_18961 20105 RMVar_ID_20105 Human_SNP_ID_46188654 A-to-I Human chr1 + 201962586 201962586 201962586 GTTGGCCAGGATGCCCTCGATCTTCTGACCTCATGATCCACCCGCCTCGGCCTCCCAAAATGCTG GTTGGCCAGGATGCCCTCGATCTTCTGACCTCGTGATCCACCCGCCTCGGCCTCCCAAAATGCTG A G TIMM17A Ensembl:ENSG00000134375 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs550900636 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_367177,RMVar_hsa_circ_18961 20106 RMVar_ID_20106 Human_SNP_ID_46194023 A-to-I Human chr1 - 201982773 201982773 201982773 ACTCAGCCCGCAGGTCCAGGTGCAAGTGCAGCAGCTCAAAGGCCCGGAAGTTGGAGGCCGAGGCC ACTCAGCCCGCAGGTCCAGGTGCAAGTGCAGCCGCTCAAAGGCCCGGAAGTTGGAGGCCGAGGCC T G - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs780885046 Functional Loss SNV dbSNP153 33..33 33 - - - 20107 RMVar_ID_20107 Human_SNP_ID_46194869 A-to-I Human chr1 + 201985491 201985491 201985491 GTTGCCCACGCTGGTCTTGAACTCCTGGGTTCAAGCCATCTGCCCGCTTTGGCATCCCAAAGTGC GTTGCCCACGCTGGTCTTGAACTCCTGGGTTCCAGCCATCTGCCCGCTTTGGCATCCCAAAGTGC A C RNPEP Ensembl:ENSG00000176393 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs972845445 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265446 20108 RMVar_ID_20108 Human_SNP_ID_46196588 A-to-I Human chr1 + 201992233 201992233 201992233 TTATTTATTTTCTGCAGGAGCAAGGTCTTGCTATGTTGTCCAGGCTGATCTTGAACTCCTGGGCT TTATTTATTTTCTGCAGGAGCAAGGTCTTGCTGTGTTGTCCAGGCTGATCTTGAACTCCTGGGCT A G RNPEP Ensembl:ENSG00000176393 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs975427054 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_138892,RMVar_hsa_circ_17858,RMVar_hsa_circ_86896,RMVar_hsa_circ_294835,RMVar_hsa_circ_329060,RMVar_hsa_circ_302797,RMVar_hsa_circ_29513,RMVar_hsa_circ_138894,RMVar_hsa_circ_138895,RMVar_hsa_circ_138896,RMVar_hsa_circ_138893 20109 RMVar_ID_20109 Human_SNP_ID_46196602 A-to-I Human chr1 + 201992294 201992294 201992294 GGCTCAAGAGATCCTCCCACCTCGGCCTCCCAAAGTGTTGGGATTGCAGGCATGAGCCACAACAC GGCTCAAGAGATCCTCCCACCTCGGCCTCCCAGAGTGTTGGGATTGCAGGCATGAGCCACAACAC A G RNPEP Ensembl:ENSG00000176393 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1376664245 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_138892,RMVar_hsa_circ_17858,RMVar_hsa_circ_86896,RMVar_hsa_circ_294835,RMVar_hsa_circ_329060,RMVar_hsa_circ_302797,RMVar_hsa_circ_29513,RMVar_hsa_circ_138894,RMVar_hsa_circ_138895,RMVar_hsa_circ_138896,RMVar_hsa_circ_138893 20110 RMVar_ID_20110 Human_SNP_ID_46197233 A-to-I Human chr1 + 201994760 201994760 201994760 GCAATCTTGGCTCCCCGCAACCTCTGCCACCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCTCA GCAATCTTGGCTCCCCGCAACCTCTGCCACCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCTCA A G RNPEP Ensembl:ENSG00000176393 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1451188299 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10726627 RMVar_hsa_circ_138892,RMVar_hsa_circ_17858,RMVar_hsa_circ_86896,RMVar_hsa_circ_294835,RMVar_hsa_circ_329060,RMVar_hsa_circ_302797,RMVar_hsa_circ_29513,RMVar_hsa_circ_138894,RMVar_hsa_circ_138895,RMVar_hsa_circ_138896,RMVar_hsa_circ_138893 20111 RMVar_ID_20111 Human_SNP_ID_46198262 A-to-I Human chr1 + 201998435 201998435 201998435 GCCCAGCTAGTTTTTATGTTTTTAGTAGAGACAGGATTTCGGCATATTGGCCAGACTGGTCTTGA GCCCAGCTAGTTTTTATGTTTTTAGTAGAGACGGGATTTCGGCATATTGGCCAGACTGGTCTTGA A G RNPEP Ensembl:ENSG00000176393 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971185081 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10726694 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 20112 RMVar_ID_20112 Human_SNP_ID_46233358 A-to-I Human chr1 - 202133931 202133931 202133931 AGAAGAGGTGCAGGCTGGCACCTGCGGCAGGTACCAGCCTGGGCACTGGTGGCCGCCTCCCTGTC AGAAGAGGTGCAGGCTGGCACCTGCGGCAGGTGCCAGCCTGGGCACTGGTGGCCGCCTCCCTGTC T C ARL8A Ensembl:ENSG00000143862 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1239352513 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_337814,Human_RBP_ID_26386837 20113 RMVar_ID_20113 Human_SNP_ID_46234934 A-to-I Human chr1 - 202139923 202139923 202139923 CAGGGCTTGGCCGGGCACCGTGGCTCACCCCTATAATCCCAGCGCTTTGGGAGGCCCAGGTAGGC CAGGGCTTGGCCGGGCACCGTGGCTCACCCCTGTAATCCCAGCGCTTTGGGAGGCCCAGGTAGGC T C ARL8A Ensembl:ENSG00000143862 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1464697059 Functional Loss SNV dbSNP153 33..33 33 - - - 20114 RMVar_ID_20114 Human_SNP_ID_46301500 A-to-I Human chr1 + 202404763 202404763 202404763 GACCTCATGATCCGCCCACCTTGGCCTCCCGGAGTGCTGGGATTACAGGCGTGAGCCACCGCACC GACCTCATGATCCGCCCACCTTGGCCTCCCGGCGTGCTGGGATTACAGGCGTGAGCCACCGCACC A C PPP1R12B Ensembl:ENSG00000077157 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1408436127 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_138922,RMVar_hsa_circ_92737 20115 RMVar_ID_20115 Human_SNP_ID_46316444 A-to-I Human chr1 + 202474382 202474382 202474382 CGATCTCACTGCAACCTCTGCCTTCCAGGTTCAAGTGATTCTCGTGCCTCAGCCTCCCCGGTAGC CGATCTCACTGCAACCTCTGCCTTCCAGGTTCGAGTGATTCTCGTGCCTCAGCCTCCCCGGTAGC A G PPP1R12B Ensembl:ENSG00000077157 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1230227982 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_138922,RMVar_hsa_circ_92737,RMVar_hsa_circ_55078,RMVar_hsa_circ_362470,RMVar_hsa_circ_40262,RMVar_hsa_circ_138930,RMVar_hsa_circ_66301,RMVar_hsa_circ_96849,RMVar_hsa_circ_341403,RMVar_hsa_circ_138932,RMVar_hsa_circ_75438,RMVar_hsa_circ_138937,RMVar_hsa_circ_138935,RMVar_hsa_circ_266708,RMVar_hsa_circ_318271,RMVar_hsa_circ_81711,RMVar_hsa_circ_283308,RMVar_hsa_circ_138936 20116 RMVar_ID_20116 Human_SNP_ID_46316480 A-to-I Human chr1 + 202474539 202474539 202474539 GCCTCGGGTAATCTGCCCGCCTCGGCCTCCTAAAATGCTGGAATTATAGGCATGAGCCACCGCGC GCCTCGGGTAATCTGCCCGCCTCGGCCTCCTAGAATGCTGGAATTATAGGCATGAGCCACCGCGC A G PPP1R12B Ensembl:ENSG00000077157 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs998181760 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_138922,RMVar_hsa_circ_92737,RMVar_hsa_circ_55078,RMVar_hsa_circ_362470,RMVar_hsa_circ_40262,RMVar_hsa_circ_138930,RMVar_hsa_circ_66301,RMVar_hsa_circ_96849,RMVar_hsa_circ_341403,RMVar_hsa_circ_138932,RMVar_hsa_circ_75438,RMVar_hsa_circ_138937,RMVar_hsa_circ_138935,RMVar_hsa_circ_266708,RMVar_hsa_circ_318271,RMVar_hsa_circ_81711,RMVar_hsa_circ_283308,RMVar_hsa_circ_138936 20117 RMVar_ID_20117 Human_SNP_ID_46328928 A-to-I Human chr1 + 202538082 202538082 202538082 ACGATCTCAAGGCTTACCGCAACCTCTGCCTCACTGTTTCAAGTGATTCTCCTGCCTCAGCCTCC ACGATCTCAAGGCTTACCGCAACCTCTGCCTCGCTGTTTCAAGTGATTCTCCTGCCTCAGCCTCC A G PPP1R12B Ensembl:ENSG00000077157 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1382575490 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96849,RMVar_hsa_circ_138932,RMVar_hsa_circ_81711,RMVar_hsa_circ_85480,RMVar_hsa_circ_138936,RMVar_hsa_circ_138940 20118 RMVar_ID_20118 Human_SNP_ID_46328933 A-to-I Human chr1 + 202538123 202538122 202538123 AGTGATTCTCCTGCCTCAGCCTCCTGTGTAGTAGCTGGGACTACAGGTGCCCCCCACAATGCCTG AGTGATTCTCCTGCCTCAGCCTCCTGTGTAGT_GCTGGGACTACAGGTGCCCCCCACAATGCCTG TA T PPP1R12B Ensembl:ENSG00000077157 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs555950771 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_96849,RMVar_hsa_circ_138932,RMVar_hsa_circ_81711,RMVar_hsa_circ_85480,RMVar_hsa_circ_138936,RMVar_hsa_circ_138940 20119 RMVar_ID_20119 Human_SNP_ID_46333915 A-to-I Human chr1 + 202563250 202563250 202563250 AGGGTCCTCCTGCCACAGCCTCCCACATAGCTAGAACTATAGCCATGCACCACCACACACGGCTA AGGGTCCTCCTGCCACAGCCTCCCACATAGCTGGAACTATAGCCATGCACCACCACACACGGCTA A G PPP1R12B Ensembl:ENSG00000077157 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1446265630 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96849,RMVar_hsa_circ_138932,RMVar_hsa_circ_76397,RMVar_hsa_circ_81711,RMVar_hsa_circ_138936,RMVar_hsa_circ_364382,RMVar_hsa_circ_97738,RMVar_hsa_circ_138942,RMVar_hsa_circ_138943,RMVar_hsa_circ_138941 20120 RMVar_ID_20120 Human_SNP_ID_46338048 A-to-I Human chr1 + 202582778 202582778 202582778 GTGGTGGCAGGCGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATGGCGTGAACCCG GTGGTGGCAGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCG A G PPP1R12B Ensembl:ENSG00000077157 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs548181494 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97738,RMVar_hsa_circ_138943,RMVar_hsa_circ_268759 20121 RMVar_ID_20121 Human_SNP_ID_46338532 A-to-I Human chr1 + 202585066 202585066 202585066 TCGCCCAGGCTGGAGTGCAGTGGTGTGATCTCAGCTCACTGCAACCTCCACCTCCCAGGCTCAAG TCGCCCAGGCTGGAGTGCAGTGGTGTGATCTCCGCTCACTGCAACCTCCACCTCCCAGGCTCAAG A C PPP1R12B Ensembl:ENSG00000077157 Protein coding 3'UTR GSE100210;GSE99789;GSE123020:GSM3490829,GSM3490830,GSM3490831 HepG2 cell line;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109 cell line - 29129909,29796672,32596459 RNA-Seq:(High) rs577560245 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_866421 RMVar_hsa_circ_97738,RMVar_hsa_circ_138943,RMVar_hsa_circ_268759 20122 RMVar_ID_20122 Human_SNP_ID_46338569 A-to-I Human chr1 + 202585197 202585197 202585197 TTTGAATTTTTTTGTAGAGATGGGGTTTTGCCATGTTGCCCAGGCTGGTCTGAAGCTGCTGGGCT TTTGAATTTTTTTGTAGAGATGGGGTTTTGCCTTGTTGCCCAGGCTGGTCTGAAGCTGCTGGGCT A T PPP1R12B Ensembl:ENSG00000077157 Protein coding 3'UTR GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831 ASD brains,cerebellum;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line - 30559470,31158229,32596459 RNA-Seq:(High) rs1450947022 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97738,RMVar_hsa_circ_138943,RMVar_hsa_circ_268759 20123 RMVar_ID_20123 Human_SNP_ID_46376600 A-to-I Human chr1 - 202741440 202741440 202741440 GGCTGGCCCCGTATTCAGCAGTGGAGAAAGCTATGGCCCGGCTGCAGGAACTGCTCACAGTGTCA GGCTGGCCCCGTATTCAGCAGTGGAGAAAGCTGTGGCCCGGCTGCAGGAACTGCTCACAGTGTCA T C KDM5B Ensembl:ENSG00000117139 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs772424958 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_851937,Human_RBP_ID_4087167,Human_RBP_ID_8740708,Human_RBP_ID_9253107,Human_RBP_ID_9270550,Human_RBP_ID_22427764 Human_Splice_Rec_174569,Human_Splice_Rec_174623,Human_Splice_Rec_174679,Human_Splice_Rec_174731,Human_Splice_Rec_174751,Human_Splice_Rec_174809,Human_Splice_Rec_174859,Human_Splice_Rec_174911,Human_Splice_Rec_174963,Human_Splice_Rec_174987,Human_Splice_Rec_175007,Human_Splice_Rec_175055,Human_Splice_Rec_175107,Human_Splice_Rec_175183,Human_Splice_Rec_175269,Human_Splice_Rec_175319 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_121952,RMVar_hsa_circ_89858,RMVar_hsa_circ_115846,RMVar_hsa_circ_77623,RMVar_hsa_circ_124590,RMVar_hsa_circ_138953,RMVar_hsa_circ_138954,RMVar_hsa_circ_138952,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 20124 RMVar_ID_20124 Human_SNP_ID_46376601 A-to-I Human chr1 - 202741440 202741440 202741440 GGCTGGCCCCGTATTCAGCAGTGGAGAAAGCTATGGCCCGGCTGCAGGAACTGCTCACAGTGTCA GGCTGGCCCCGTATTCAGCAGTGGAGAAAGCTCTGGCCCGGCTGCAGGAACTGCTCACAGTGTCA T G KDM5B Ensembl:ENSG00000117139 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs772424958 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_851937,Human_RBP_ID_4087167,Human_RBP_ID_8740708,Human_RBP_ID_9253107,Human_RBP_ID_9270550,Human_RBP_ID_22427764 Human_Splice_Rec_174569,Human_Splice_Rec_174623,Human_Splice_Rec_174679,Human_Splice_Rec_174731,Human_Splice_Rec_174751,Human_Splice_Rec_174809,Human_Splice_Rec_174859,Human_Splice_Rec_174911,Human_Splice_Rec_174963,Human_Splice_Rec_174987,Human_Splice_Rec_175007,Human_Splice_Rec_175055,Human_Splice_Rec_175107,Human_Splice_Rec_175183,Human_Splice_Rec_175269,Human_Splice_Rec_175319 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_121952,RMVar_hsa_circ_89858,RMVar_hsa_circ_115846,RMVar_hsa_circ_77623,RMVar_hsa_circ_124590,RMVar_hsa_circ_138953,RMVar_hsa_circ_138954,RMVar_hsa_circ_138952,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 20125 RMVar_ID_20125 Human_SNP_ID_46386497 A-to-I Human chr1 - 202778901 202778901 202778901 AATAGAGATCTAGGCTGGGTGCGGTGGCTCACACTTGTAATCCCGGCACTTTGGGAGGCCGAGGC AATAGAGATCTAGGCTGGGTGCGGTGGCTCACGCTTGTAATCCCGGCACTTTGGGAGGCCGAGGC T C KDM5B Ensembl:ENSG00000117139 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1284495627 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92149,RMVar_hsa_circ_138986,RMVar_hsa_circ_101922,RMVar_hsa_circ_139000 20126 RMVar_ID_20126 Human_SNP_ID_46388656 A-to-I Human chr1 - 202787292 202787286 202787293 TAAAAAGGGAAACTTGGTCGGATGGGTGGCTCACACCTGTAATCTCAGCACTTTGGGAGGCCAAA TAAAAAGGGAAACTTGGTCGGATGGGTGGCT_______GTAATCTCAGCACTTTGGGAGGCCAAA CAGGTGTG C KDM5B Ensembl:ENSG00000117139 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1246077599 Functional Loss DEL dbSNP153 32..38 33 - - - RMVar_hsa_circ_92149,RMVar_hsa_circ_138986,RMVar_hsa_circ_101922,RMVar_hsa_circ_139000 20127 RMVar_ID_20127 Human_SNP_ID_46389871 A-to-I Human chr1 - 202791875 202791875 202791875 GTCTCTACTAAAAATATAAAAATTAGCTGGGCATGGTGGCATGTACCTGTAGTCCCAGCTACTCC GTCTCTACTAAAAATATAAAAATTAGCTGGGCGTGGTGGCATGTACCTGTAGTCCCAGCTACTCC T C KDM5B Ensembl:ENSG00000117139 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1050471037 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92149,RMVar_hsa_circ_138986,RMVar_hsa_circ_101922,RMVar_hsa_circ_139000 20128 RMVar_ID_20128 Human_SNP_ID_46411030 A-to-I Human chr1 - 202876170 202876166 202876170 TAAGGTTTTTATTTTTCTTGGGACAGGGCCTCACTCTGTCACCGAGGCTGGAGCGCAATGGCACG TAAGGTTTTTATTTTTCTTGGGACAGGGCCTC____TGTCACCGAGGCTGGAGCGCAATGGCACG AGAGT A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1169408344 Functional Loss DEL dbSNP153 33..36 33 - - - 20129 RMVar_ID_20129 Human_SNP_ID_46411034 A-to-I Human chr1 - 202876178 202876176 202876178 TTTCACAATAAGGTTTTTATTTTTCTTGGGACAGGGCCTCACTCTGTCACCGAGGCTGGAGCGCA TTTCACAATAAGGTTTTTATTTTTCTTGGGAC__GGCCTCACTCTGTCACCGAGGCTGGAGCGCA CCT C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1240484594 Functional Loss DEL dbSNP153 33..34 33 - - - 20130 RMVar_ID_20130 Human_SNP_ID_46411035 A-to-I Human chr1 - 202876178 202876178 202876178 TTTCACAATAAGGTTTTTATTTTTCTTGGGACAGGGCCTCACTCTGTCACCGAGGCTGGAGCGCA TTTCACAATAAGGTTTTTATTTTTCTTGGGACGGGGCCTCACTCTGTCACCGAGGCTGGAGCGCA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs547029007 Functional Loss SNV dbSNP153 33..33 33 - - - 20131 RMVar_ID_20131 Human_SNP_ID_46419020 A-to-I Human chr1 - 202907910 202907910 202907910 GGTGATTTATCCGCTATATTTTATTTTTTTTAATAGAAATGAGGTCTCACTATGTTGCCCAGGGT GGTGATTTATCCGCTATATTTTATTTTTTTTAGTAGAAATGAGGTCTCACTATGTTGCCCAGGGT T C KLHL12 Ensembl:ENSG00000117153 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs914281697 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5740361 RMVar_hsa_circ_139013,RMVar_hsa_circ_345973 20132 RMVar_ID_20132 Human_SNP_ID_46429803 A-to-I Human chr1 - 202950356 202950356 202950356 TTGCCTAGGCTGATCTTAAACTCCTAGGCTCAAGTGATCCTCCTGCCTCAGCCTCCCAAAGTGTT TTGCCTAGGCTGATCTTAAACTCCTAGGCTCAGGTGATCCTCCTGCCTCAGCCTCCCAAAGTGTT T C ADIPOR1 Ensembl:ENSG00000159346 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs987694274 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44820,RMVar_hsa_circ_268295,RMVar_hsa_circ_56413,RMVar_hsa_circ_57249,RMVar_hsa_circ_347464 20133 RMVar_ID_20133 Human_SNP_ID_46429805 A-to-I Human chr1 - 202950363 202950363 202950363 CGCCATGTTGCCTAGGCTGATCTTAAACTCCTAGGCTCAAGTGATCCTCCTGCCTCAGCCTCCCA CGCCATGTTGCCTAGGCTGATCTTAAACTCCTGGGCTCAAGTGATCCTCCTGCCTCAGCCTCCCA T C ADIPOR1 Ensembl:ENSG00000159346 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs940669408 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44820,RMVar_hsa_circ_268295,RMVar_hsa_circ_56413,RMVar_hsa_circ_57249,RMVar_hsa_circ_347464 20134 RMVar_ID_20134 Human_SNP_ID_46432512 A-to-I Human chr1 - 202962456 202962456 202962456 TTCCCCATCAGTACTCAAGCACTATAAGCCTTAGATTCCTTTCCTCAGAGTTTCAGGTTTTTTCA TTCCCCATCAGTACTCAAGCACTATAAGCCTTGGATTCCTTTCCTCAGAGTTTCAGGTTTTTTCA T C CYB5R1 Ensembl:ENSG00000159348 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs563292426 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95119,RMVar_hsa_circ_139019 20135 RMVar_ID_20135 Human_SNP_ID_46432513 A-to-I Human chr1 - 202962456 202962456 202962456 TTCCCCATCAGTACTCAAGCACTATAAGCCTTAGATTCCTTTCCTCAGAGTTTCAGGTTTTTTCA TTCCCCATCAGTACTCAAGCACTATAAGCCTTCGATTCCTTTCCTCAGAGTTTCAGGTTTTTTCA T G CYB5R1 Ensembl:ENSG00000159348 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs563292426 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95119,RMVar_hsa_circ_139019 20136 RMVar_ID_20136 Human_SNP_ID_46432739 A-to-I Human chr1 - 202963108 202963108 202963108 AGGACTTAGAGGAACTGCAGGCCCGCTATCCCAATCGCTTTAAGCTCTGGTTCACTCTGGATCAT AGGACTTAGAGGAACTGCAGGCCCGCTATCCCGATCGCTTTAAGCTCTGGTTCACTCTGGATCAT T C CYB5R1 Ensembl:ENSG00000159348 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1247995967 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22752174,Human_RBP_ID_26799356 Human_Splice_Rec_175572,Human_Splice_Rec_175573,Human_Splice_Rec_175576,Human_Splice_Rec_175588,Human_Splice_Rec_175589,Human_Splice_Rec_175591,Human_Splice_Rec_175602 RMVar_hsa_circ_95119,RMVar_hsa_circ_21102,RMVar_hsa_circ_139019,RMVar_hsa_circ_367911,RMVar_hsa_circ_139020 20137 RMVar_ID_20137 Human_SNP_ID_46445923 A-to-I Human chr1 + 203014482 203014482 203014482 AAAATTTGCTGGGTGCGGTGGAGTGTGCCTGTAGTCCTAGCTACTCTGGTGGCTGAGGCATGAGA AAAATTTGCTGGGTGCGGTGGAGTGTGCCTGTGGTCCTAGCTACTCTGGTGGCTGAGGCATGAGA A G TMEM183A Ensembl:ENSG00000163444 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1233859392 Functional Loss SNV dbSNP153 33..33 33 - - - 20138 RMVar_ID_20138 Human_SNP_ID_46447151 A-to-I Human chr1 + 203019619 203019619 203019619 TTAAGTCACCTTTACTTTGTCAATATATTTATATATTATTTAAGCTTATTTACCATTAAAAAAAG TTAAGTCACCTTTACTTTGTCAATATATTTATGTATTATTTAAGCTTATTTACCATTAAAAAAAG A G TMEM183A Ensembl:ENSG00000163444 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs564612852 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5740556 20139 RMVar_ID_20139 Human_SNP_ID_46447906 A-to-I Human chr1 + 203022628 203022628 203022628 GGGAGGCTGAGGCACAAGAATCGTTTGATCCCAGGAGGCGGAGGTTGCAGTGAGCCGAGATCACA GGGAGGCTGAGGCACAAGAATCGTTTGATCCCGGGAGGCGGAGGTTGCAGTGAGCCGAGATCACA A G TMEM183A Ensembl:ENSG00000163444 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1338674604 Functional Loss SNV dbSNP153 33..33 33 - - - 20140 RMVar_ID_20140 Human_SNP_ID_46447925 A-to-I Human chr1 + 203022687 203022687 203022687 ATCACATCACTGCACTACAGCCTGGGCAACAGAACGAGGTCCTTTCTCAAAAAAAAAAAAAAAAG ATCACATCACTGCACTACAGCCTGGGCAACAGGACGAGGTCCTTTCTCAAAAAAAAAAAAAAAAG A G TMEM183A Ensembl:ENSG00000163444 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs796395381 Functional Loss SNV dbSNP153 33..33 33 - - - 20141 RMVar_ID_20141 Human_SNP_ID_46448281 A-to-I Human chr1 + 203024029 203024029 203024029 ATCTTTTAAATATGTATTTCTGAATAAAATGTAAAACCAAGAAAGTTATTTCAGGAAGGATAGTG ATCTTTTAAATATGTATTTCTGAATAAAATGTGAAACCAAGAAAGTTATTTCAGGAAGGATAGTG A G TMEM183A Ensembl:ENSG00000163444 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1172408541 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_338153,Human_RBP_ID_1733438,Human_RBP_ID_2115917 20142 RMVar_ID_20142 Human_SNP_ID_46529962 A-to-I Human chr1 - 203353724 203353724 203353724 AGGTCGGAGCCACTGCTGTCACCATGACCCGCAGTAACCAGCATGAGCTTACTGGCTAGAAAAAT AGGTCGGAGCCACTGCTGTCACCATGACCCGCGGTAACCAGCATGAGCTTACTGGCTAGAAAAAT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984200476 Functional Loss SNV dbSNP153 33..33 33 - - - 20143 RMVar_ID_20143 Human_SNP_ID_46643210 A-to-I Human chr1 + 203804420 203804420 203804420 GTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTAGGATTACAAGCATGAGCCACCACGCCCGGCCC GTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAAGCATGAGCCACCACGCCCGGCCC A G ZC3H11A,ZBED6 Ensembl:ENSG00000058673,Ensembl:ENSG00000257315 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1374618677 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15438,RMVar_hsa_circ_127735,RMVar_hsa_circ_33437,RMVar_hsa_circ_139077,RMVar_hsa_circ_43929,RMVar_hsa_circ_70230,RMVar_hsa_circ_24649,RMVar_hsa_circ_51852 20144 RMVar_ID_20144 Human_SNP_ID_46643460 A-to-I Human chr1 + 203805233 203805233 203805233 CTTGGCTCACTGGACCTCCGCCTCCTGGGTTCAAGCAATTCTCCTGCTTCAGTCTCCCGAGAGTA CTTGGCTCACTGGACCTCCGCCTCCTGGGTTCGAGCAATTCTCCTGCTTCAGTCTCCCGAGAGTA A G ZC3H11A,ZBED6 Ensembl:ENSG00000058673,Ensembl:ENSG00000257315 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005619824 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10731593 RMVar_hsa_circ_15438,RMVar_hsa_circ_127735,RMVar_hsa_circ_33437,RMVar_hsa_circ_139077,RMVar_hsa_circ_43929,RMVar_hsa_circ_70230,RMVar_hsa_circ_24649,RMVar_hsa_circ_51852 20145 RMVar_ID_20145 Human_SNP_ID_46643461 A-to-I Human chr1 + 203805233 203805233 203805233 CTTGGCTCACTGGACCTCCGCCTCCTGGGTTCAAGCAATTCTCCTGCTTCAGTCTCCCGAGAGTA CTTGGCTCACTGGACCTCCGCCTCCTGGGTTCTAGCAATTCTCCTGCTTCAGTCTCCCGAGAGTA A T ZC3H11A,ZBED6 Ensembl:ENSG00000058673,Ensembl:ENSG00000257315 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005619824 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10731593 RMVar_hsa_circ_15438,RMVar_hsa_circ_127735,RMVar_hsa_circ_33437,RMVar_hsa_circ_139077,RMVar_hsa_circ_43929,RMVar_hsa_circ_70230,RMVar_hsa_circ_24649,RMVar_hsa_circ_51852 20146 RMVar_ID_20146 Human_SNP_ID_46643473 A-to-I Human chr1 + 203805271 203805271 203805271 TTCTCCTGCTTCAGTCTCCCGAGAGTAGGACTACAGGCGCCCGCCACCACACCCGGCTAATTTTT TTCTCCTGCTTCAGTCTCCCGAGAGTAGGACTGCAGGCGCCCGCCACCACACCCGGCTAATTTTT A G ZC3H11A,ZBED6 Ensembl:ENSG00000058673,Ensembl:ENSG00000257315 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432417149 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10731593 RMVar_hsa_circ_15438,RMVar_hsa_circ_127735,RMVar_hsa_circ_33437,RMVar_hsa_circ_139077,RMVar_hsa_circ_43929,RMVar_hsa_circ_70230,RMVar_hsa_circ_24649,RMVar_hsa_circ_51852 20147 RMVar_ID_20147 Human_SNP_ID_46644680 A-to-I Human chr1 + 203809767 203809767 203809767 CTTGAGGTCAGGAGTTCGAGACCAATCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATAC CTTGAGGTCAGGAGTTCGAGACCAATCTGGCCCACATGGTGAAACCCCGTCTCTACTAAAAATAC A C ZC3H11A,ZBED6 Ensembl:ENSG00000058673,Ensembl:ENSG00000257315 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1162473113 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15438,RMVar_hsa_circ_127735,RMVar_hsa_circ_33437,RMVar_hsa_circ_139077,RMVar_hsa_circ_43929,RMVar_hsa_circ_70230,RMVar_hsa_circ_24649,RMVar_hsa_circ_51852 20148 RMVar_ID_20148 Human_SNP_ID_46644682 A-to-I Human chr1 + 203809770 203809770 203809770 GAGGTCAGGAGTTCGAGACCAATCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAA GAGGTCAGGAGTTCGAGACCAATCTGGCCAACGTGGTGAAACCCCGTCTCTACTAAAAATACAAA A G ZC3H11A,ZBED6 Ensembl:ENSG00000058673,Ensembl:ENSG00000257315 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1418449700 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15438,RMVar_hsa_circ_127735,RMVar_hsa_circ_33437,RMVar_hsa_circ_139077,RMVar_hsa_circ_43929,RMVar_hsa_circ_70230,RMVar_hsa_circ_24649,RMVar_hsa_circ_51852 20149 RMVar_ID_20149 Human_SNP_ID_46644683 A-to-I Human chr1 + 203809770 203809770 203809770 GAGGTCAGGAGTTCGAGACCAATCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAA GAGGTCAGGAGTTCGAGACCAATCTGGCCAACTTGGTGAAACCCCGTCTCTACTAAAAATACAAA A T ZC3H11A,ZBED6 Ensembl:ENSG00000058673,Ensembl:ENSG00000257315 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1418449700 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15438,RMVar_hsa_circ_127735,RMVar_hsa_circ_33437,RMVar_hsa_circ_139077,RMVar_hsa_circ_43929,RMVar_hsa_circ_70230,RMVar_hsa_circ_24649,RMVar_hsa_circ_51852 20150 RMVar_ID_20150 Human_SNP_ID_46644712 A-to-I Human chr1 + 203809879 203809879 203809879 GGGAGGGTGAGGCAGGAGAATTGCTTGAACCCAGGAGGTGGAGGTTGCAGTAAGTCAAGATCACG GGGAGGGTGAGGCAGGAGAATTGCTTGAACCCGGGAGGTGGAGGTTGCAGTAAGTCAAGATCACG A G ZC3H11A,ZBED6 Ensembl:ENSG00000058673,Ensembl:ENSG00000257315 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1158616104 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15438,RMVar_hsa_circ_127735,RMVar_hsa_circ_33437,RMVar_hsa_circ_139077,RMVar_hsa_circ_43929,RMVar_hsa_circ_70230,RMVar_hsa_circ_24649,RMVar_hsa_circ_51852 20151 RMVar_ID_20151 Human_SNP_ID_46644915 A-to-I Human chr1 + 203810489 203810489 203810489 TCGCCCAGGCTAGAGTGCAGTGGCGCGATCTCAGCTCACTGCAACCTGCACCTCTGGGGTTCACA TCGCCCAGGCTAGAGTGCAGTGGCGCGATCTCTGCTCACTGCAACCTGCACCTCTGGGGTTCACA A T ZC3H11A,ZBED6 Ensembl:ENSG00000058673,Ensembl:ENSG00000257315 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1435669747 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15438,RMVar_hsa_circ_127735,RMVar_hsa_circ_33437,RMVar_hsa_circ_139077,RMVar_hsa_circ_43929,RMVar_hsa_circ_70230,RMVar_hsa_circ_24649,RMVar_hsa_circ_51852 20152 RMVar_ID_20152 Human_SNP_ID_46645055 A-to-I Human chr1 + 203810994 203810994 203810994 CTCTACTAAAAATACAAAAAAAAAAAAAAATTAGCAGGGTATGGTGGTAGGCGCCTGTAATCCCA CTCTACTAAAAATACAAAAAAAAAAAAAAATTGGCAGGGTATGGTGGTAGGCGCCTGTAATCCCA A G ZC3H11A,ZBED6 Ensembl:ENSG00000058673,Ensembl:ENSG00000257315 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1379618642 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15438,RMVar_hsa_circ_127735,RMVar_hsa_circ_33437,RMVar_hsa_circ_139077,RMVar_hsa_circ_43929,RMVar_hsa_circ_70230,RMVar_hsa_circ_24649,RMVar_hsa_circ_51852 20153 RMVar_ID_20153 Human_SNP_ID_46645313 A-to-I Human chr1 + 203811955 203811955 203811955 CTCACACCTCAGCCTCCTGAGTAGCTGGGACTATAGATGTGTGCCACCATGCTTGGCTAATTTTT CTCACACCTCAGCCTCCTGAGTAGCTGGGACTGTAGATGTGTGCCACCATGCTTGGCTAATTTTT A G ZC3H11A,ZBED6 Ensembl:ENSG00000058673,Ensembl:ENSG00000257315 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1008845621 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15438,RMVar_hsa_circ_127735,RMVar_hsa_circ_33437,RMVar_hsa_circ_139077,RMVar_hsa_circ_43929,RMVar_hsa_circ_70230,RMVar_hsa_circ_24649,RMVar_hsa_circ_51852 20154 RMVar_ID_20154 Human_SNP_ID_46645867 A-to-I Human chr1 + 203814260 203814260 203814260 CAGGAATAACCTTTCCGGCCAGGCGCTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAG CAGGAATAACCTTTCCGGCCAGGCGCTGGCTCCCACCTGTAATCCCAGCACTTTGGGAGGCTGAG A C ZC3H11A,ZBED6 Ensembl:ENSG00000058673,Ensembl:ENSG00000257315 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1230354012 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24624490 RMVar_hsa_circ_15438,RMVar_hsa_circ_127735,RMVar_hsa_circ_33437,RMVar_hsa_circ_139077,RMVar_hsa_circ_43929,RMVar_hsa_circ_70230,RMVar_hsa_circ_24649,RMVar_hsa_circ_51852 20155 RMVar_ID_20155 Human_SNP_ID_46646461 A-to-I Human chr1 + 203816442 203816442 203816442 AGGCAGGAGTTCAAGACCAGACTGAACAACATAGCAAGATCCTGTCTTTACAAAAATTTTTTTTA AGGCAGGAGTTCAAGACCAGACTGAACAACATGGCAAGATCCTGTCTTTACAAAAATTTTTTTTA A G ZC3H11A,ZBED6 Ensembl:ENSG00000058673,Ensembl:ENSG00000257315 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1310857633 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15438,RMVar_hsa_circ_127735,RMVar_hsa_circ_33437,RMVar_hsa_circ_139077,RMVar_hsa_circ_43929,RMVar_hsa_circ_70230,RMVar_hsa_circ_24649,RMVar_hsa_circ_51852 20156 RMVar_ID_20156 Human_SNP_ID_46647569 A-to-I Human chr1 + 203819981 203819981 203819981 AGTCCAGGCTGGGCTCAGTGGCTCACGCCTGTAATCCCAGCACTTTACTAGGCTGAGGCGGGTGA AGTCCAGGCTGGGCTCAGTGGCTCACGCCTGTGATCCCAGCACTTTACTAGGCTGAGGCGGGTGA A G ZC3H11A,ZBED6 Ensembl:ENSG00000058673,Ensembl:ENSG00000257315 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1452096295 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15438,RMVar_hsa_circ_127735,RMVar_hsa_circ_139077,RMVar_hsa_circ_43929,RMVar_hsa_circ_24649,RMVar_hsa_circ_139080,RMVar_hsa_circ_335111,RMVar_hsa_circ_349527,RMVar_hsa_circ_51852,RMVar_hsa_circ_339623,RMVar_hsa_circ_92032,RMVar_hsa_circ_272982,RMVar_hsa_circ_89302,RMVar_hsa_circ_139081 20157 RMVar_ID_20157 Human_SNP_ID_46648147 A-to-I Human chr1 + 203821897 203821897 203821897 CTCCTGTTTCAGTCTCCCGAGTAGCTGGGATTACAGGTGCCCGCCACCACGCCCGGCTAATTTTT CTCCTGTTTCAGTCTCCCGAGTAGCTGGGATTCCAGGTGCCCGCCACCACGCCCGGCTAATTTTT A C ZC3H11A,ZBED6 Ensembl:ENSG00000058673,Ensembl:ENSG00000257315 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs754558487 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15438,RMVar_hsa_circ_127735,RMVar_hsa_circ_139077,RMVar_hsa_circ_43929,RMVar_hsa_circ_24649,RMVar_hsa_circ_139080,RMVar_hsa_circ_335111,RMVar_hsa_circ_349527,RMVar_hsa_circ_51852,RMVar_hsa_circ_339623,RMVar_hsa_circ_92032,RMVar_hsa_circ_272982,RMVar_hsa_circ_89302,RMVar_hsa_circ_139081 20158 RMVar_ID_20158 Human_SNP_ID_46648148 A-to-I Human chr1 + 203821899 203821899 203821899 CCTGTTTCAGTCTCCCGAGTAGCTGGGATTACAGGTGCCCGCCACCACGCCCGGCTAATTTTTTG CCTGTTTCAGTCTCCCGAGTAGCTGGGATTACTGGTGCCCGCCACCACGCCCGGCTAATTTTTTG A T ZC3H11A,ZBED6 Ensembl:ENSG00000058673,Ensembl:ENSG00000257315 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1173415323 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15438,RMVar_hsa_circ_127735,RMVar_hsa_circ_139077,RMVar_hsa_circ_43929,RMVar_hsa_circ_24649,RMVar_hsa_circ_139080,RMVar_hsa_circ_335111,RMVar_hsa_circ_349527,RMVar_hsa_circ_51852,RMVar_hsa_circ_339623,RMVar_hsa_circ_92032,RMVar_hsa_circ_272982,RMVar_hsa_circ_89302,RMVar_hsa_circ_139081 20159 RMVar_ID_20159 Human_SNP_ID_46648886 A-to-I Human chr1 + 203824824 203824824 203824824 TTGTTAGGCCGGACACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGCAG TTGTTAGGCCGGACACGGTGGCTCACGCCTGTGATCCCAGCACTTTGGGAGGCTGAGGCAGGCAG A G ZC3H11A,ZBED6 Ensembl:ENSG00000058673,Ensembl:ENSG00000257315 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1337218161 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15438,RMVar_hsa_circ_127735,RMVar_hsa_circ_139077,RMVar_hsa_circ_43929,RMVar_hsa_circ_24649,RMVar_hsa_circ_139080,RMVar_hsa_circ_335111,RMVar_hsa_circ_349527,RMVar_hsa_circ_51852,RMVar_hsa_circ_339623,RMVar_hsa_circ_92032,RMVar_hsa_circ_272982,RMVar_hsa_circ_89302,RMVar_hsa_circ_139081 20160 RMVar_ID_20160 Human_SNP_ID_46648921 A-to-I Human chr1 + 203824954 203824954 203824954 AAAAAATTAGCCGGGCATGGTGACACGTGCCTATAATCCCAGCTACTCGGGAGGCTGAGGCAGGA AAAAAATTAGCCGGGCATGGTGACACGTGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGA A G ZC3H11A,ZBED6 Ensembl:ENSG00000058673,Ensembl:ENSG00000257315 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs867078809 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24624577 RMVar_hsa_circ_15438,RMVar_hsa_circ_127735,RMVar_hsa_circ_139077,RMVar_hsa_circ_43929,RMVar_hsa_circ_24649,RMVar_hsa_circ_139080,RMVar_hsa_circ_335111,RMVar_hsa_circ_349527,RMVar_hsa_circ_51852,RMVar_hsa_circ_339623,RMVar_hsa_circ_92032,RMVar_hsa_circ_272982,RMVar_hsa_circ_89302,RMVar_hsa_circ_139081 20161 RMVar_ID_20161 Human_SNP_ID_46649115 A-to-I Human chr1 + 203825619 203825619 203825619 ACCATGCCCAGCTAATTTTTGTATTTTTTAGTAGAGACGGGGTTTCACCATATTGGTCAGGCTCC ACCATGCCCAGCTAATTTTTGTATTTTTTAGTGGAGACGGGGTTTCACCATATTGGTCAGGCTCC A G ZC3H11A,ZBED6 Ensembl:ENSG00000058673,Ensembl:ENSG00000257315 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1028849487 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15438,RMVar_hsa_circ_127735,RMVar_hsa_circ_139077,RMVar_hsa_circ_43929,RMVar_hsa_circ_24649,RMVar_hsa_circ_139080,RMVar_hsa_circ_335111,RMVar_hsa_circ_349527,RMVar_hsa_circ_51852,RMVar_hsa_circ_339623,RMVar_hsa_circ_92032,RMVar_hsa_circ_272982,RMVar_hsa_circ_89302,RMVar_hsa_circ_139081 20162 RMVar_ID_20162 Human_SNP_ID_46650292 A-to-I Human chr1 + 203830662 203830662 203830662 GTGAAACCCCGTCTCTACTAAAACAAAAAATTAGCCAGGCGGGGTGGCATGCACCTGTAGTCCCA GTGAAACCCCGTCTCTACTAAAACAAAAAATTGGCCAGGCGGGGTGGCATGCACCTGTAGTCCCA A G ZC3H11A,ZBED6 Ensembl:ENSG00000058673,Ensembl:ENSG00000257315 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1253108529 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15438,RMVar_hsa_circ_127735,RMVar_hsa_circ_139077,RMVar_hsa_circ_43929,RMVar_hsa_circ_24649,RMVar_hsa_circ_335111,RMVar_hsa_circ_349527,RMVar_hsa_circ_51852,RMVar_hsa_circ_339623,RMVar_hsa_circ_272982,RMVar_hsa_circ_73173,RMVar_hsa_circ_324897,RMVar_hsa_circ_355155,RMVar_hsa_circ_319370,RMVar_hsa_circ_65402,RMVar_hsa_circ_81522,RMVar_hsa_circ_119203,RMVar_hsa_circ_139082,RMVar_hsa_circ_20954,RMVar_hsa_circ_139083,RMVar_hsa_circ_110721,RMVar_hsa_circ_139084,RMVar_hsa_circ_139085 20163 RMVar_ID_20163 Human_SNP_ID_46650312 A-to-I Human chr1 + 203830750 203830750 203830750 AGAATTGCTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCTGAGATCGCACCATTGTATTCCAGCC AGAATTGCTTGAACCCAGGAGGCAGAGGTTGCGGTGAGCTGAGATCGCACCATTGTATTCCAGCC A G ZC3H11A,ZBED6 Ensembl:ENSG00000058673,Ensembl:ENSG00000257315 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1166826165 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15438,RMVar_hsa_circ_127735,RMVar_hsa_circ_139077,RMVar_hsa_circ_43929,RMVar_hsa_circ_24649,RMVar_hsa_circ_335111,RMVar_hsa_circ_349527,RMVar_hsa_circ_51852,RMVar_hsa_circ_339623,RMVar_hsa_circ_272982,RMVar_hsa_circ_73173,RMVar_hsa_circ_324897,RMVar_hsa_circ_355155,RMVar_hsa_circ_319370,RMVar_hsa_circ_65402,RMVar_hsa_circ_81522,RMVar_hsa_circ_119203,RMVar_hsa_circ_139082,RMVar_hsa_circ_20954,RMVar_hsa_circ_139083,RMVar_hsa_circ_110721,RMVar_hsa_circ_139084,RMVar_hsa_circ_139085 20164 RMVar_ID_20164 Human_SNP_ID_46650434 A-to-I Human chr1 + 203831044 203831044 203831044 CTTTGCTCACCACAACCTCCACCTCCCAGTTCAAGCTATTCTGCTGCCTCAGCCTCCTGAGTAGC CTTTGCTCACCACAACCTCCACCTCCCAGTTCGAGCTATTCTGCTGCCTCAGCCTCCTGAGTAGC A G ZC3H11A,ZBED6 Ensembl:ENSG00000058673,Ensembl:ENSG00000257315 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1282092249 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15438,RMVar_hsa_circ_127735,RMVar_hsa_circ_139077,RMVar_hsa_circ_43929,RMVar_hsa_circ_24649,RMVar_hsa_circ_335111,RMVar_hsa_circ_349527,RMVar_hsa_circ_51852,RMVar_hsa_circ_339623,RMVar_hsa_circ_272982,RMVar_hsa_circ_73173,RMVar_hsa_circ_324897,RMVar_hsa_circ_355155,RMVar_hsa_circ_319370,RMVar_hsa_circ_65402,RMVar_hsa_circ_81522,RMVar_hsa_circ_119203,RMVar_hsa_circ_139082,RMVar_hsa_circ_20954,RMVar_hsa_circ_139083,RMVar_hsa_circ_110721,RMVar_hsa_circ_139084,RMVar_hsa_circ_139085 20165 RMVar_ID_20165 Human_SNP_ID_46650436 A-to-I Human chr1 + 203831049 203831049 203831049 CTCACCACAACCTCCACCTCCCAGTTCAAGCTATTCTGCTGCCTCAGCCTCCTGAGTAGCTGGGA CTCACCACAACCTCCACCTCCCAGTTCAAGCTGTTCTGCTGCCTCAGCCTCCTGAGTAGCTGGGA A G ZC3H11A,ZBED6 Ensembl:ENSG00000058673,Ensembl:ENSG00000257315 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1306458289 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15438,RMVar_hsa_circ_127735,RMVar_hsa_circ_139077,RMVar_hsa_circ_43929,RMVar_hsa_circ_24649,RMVar_hsa_circ_335111,RMVar_hsa_circ_349527,RMVar_hsa_circ_51852,RMVar_hsa_circ_339623,RMVar_hsa_circ_272982,RMVar_hsa_circ_73173,RMVar_hsa_circ_324897,RMVar_hsa_circ_355155,RMVar_hsa_circ_319370,RMVar_hsa_circ_65402,RMVar_hsa_circ_81522,RMVar_hsa_circ_119203,RMVar_hsa_circ_139082,RMVar_hsa_circ_20954,RMVar_hsa_circ_139083,RMVar_hsa_circ_110721,RMVar_hsa_circ_139084,RMVar_hsa_circ_139085 20166 RMVar_ID_20166 Human_SNP_ID_46650732 A-to-I Human chr1 + 203832244 203832243 203832245 CCAAGCCCGGCTGATTTTTTTGTATTTTTAGTAGAGACGGGGTTTCTCCATGTTGGTCTGGCTGG CCAAGCCCGGCTGATTTTTTTGTATTTTTAGT__AGACGGGGTTTCTCCATGTTGGTCTGGCTGG TAG T ZC3H11A,ZBED6 Ensembl:ENSG00000058673,Ensembl:ENSG00000257315 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1353856071 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_15438,RMVar_hsa_circ_127735,RMVar_hsa_circ_139077,RMVar_hsa_circ_43929,RMVar_hsa_circ_24649,RMVar_hsa_circ_335111,RMVar_hsa_circ_349527,RMVar_hsa_circ_51852,RMVar_hsa_circ_272982,RMVar_hsa_circ_73173,RMVar_hsa_circ_324897,RMVar_hsa_circ_319370,RMVar_hsa_circ_65402,RMVar_hsa_circ_81522,RMVar_hsa_circ_119203,RMVar_hsa_circ_139082,RMVar_hsa_circ_20954,RMVar_hsa_circ_139083,RMVar_hsa_circ_75443,RMVar_hsa_circ_110721,RMVar_hsa_circ_139084,RMVar_hsa_circ_139085,RMVar_hsa_circ_370798,RMVar_hsa_circ_139086 20167 RMVar_ID_20167 Human_SNP_ID_46651091 A-to-I Human chr1 + 203833420 203833420 203833420 CAGGTGTGGTAGTGTGCGCAGTAGTCCCAGCTACTTGGGAGGCTGAGACAGGAGAATTGCTTGAA CAGGTGTGGTAGTGTGCGCAGTAGTCCCAGCTGCTTGGGAGGCTGAGACAGGAGAATTGCTTGAA A G ZC3H11A,ZBED6 Ensembl:ENSG00000058673,Ensembl:ENSG00000257315 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1337792600 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15438,RMVar_hsa_circ_127735,RMVar_hsa_circ_139077,RMVar_hsa_circ_43929,RMVar_hsa_circ_24649,RMVar_hsa_circ_335111,RMVar_hsa_circ_349527,RMVar_hsa_circ_51852,RMVar_hsa_circ_272982,RMVar_hsa_circ_73173,RMVar_hsa_circ_324897,RMVar_hsa_circ_319370,RMVar_hsa_circ_65402,RMVar_hsa_circ_81522,RMVar_hsa_circ_119203,RMVar_hsa_circ_139082,RMVar_hsa_circ_20954,RMVar_hsa_circ_139083,RMVar_hsa_circ_75443,RMVar_hsa_circ_110721,RMVar_hsa_circ_139084,RMVar_hsa_circ_139085,RMVar_hsa_circ_370798,RMVar_hsa_circ_139086 20168 RMVar_ID_20168 Human_SNP_ID_46651092 A-to-I Human chr1 + 203833420 203833420 203833420 CAGGTGTGGTAGTGTGCGCAGTAGTCCCAGCTACTTGGGAGGCTGAGACAGGAGAATTGCTTGAA CAGGTGTGGTAGTGTGCGCAGTAGTCCCAGCTTCTTGGGAGGCTGAGACAGGAGAATTGCTTGAA A T ZC3H11A,ZBED6 Ensembl:ENSG00000058673,Ensembl:ENSG00000257315 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1337792600 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15438,RMVar_hsa_circ_127735,RMVar_hsa_circ_139077,RMVar_hsa_circ_43929,RMVar_hsa_circ_24649,RMVar_hsa_circ_335111,RMVar_hsa_circ_349527,RMVar_hsa_circ_51852,RMVar_hsa_circ_272982,RMVar_hsa_circ_73173,RMVar_hsa_circ_324897,RMVar_hsa_circ_319370,RMVar_hsa_circ_65402,RMVar_hsa_circ_81522,RMVar_hsa_circ_119203,RMVar_hsa_circ_139082,RMVar_hsa_circ_20954,RMVar_hsa_circ_139083,RMVar_hsa_circ_75443,RMVar_hsa_circ_110721,RMVar_hsa_circ_139084,RMVar_hsa_circ_139085,RMVar_hsa_circ_370798,RMVar_hsa_circ_139086 20169 RMVar_ID_20169 Human_SNP_ID_46651909 A-to-I Human chr1 + 203836481 203836481 203836481 CAGTGTAATAAAACTAGAAGGCTGGGCGCGGTAGCTTACGCCTGTAATCCCAGCACTTTGAGAGG CAGTGTAATAAAACTAGAAGGCTGGGCGCGGTGGCTTACGCCTGTAATCCCAGCACTTTGAGAGG A G ZC3H11A,ZBED6 Ensembl:ENSG00000058673,Ensembl:ENSG00000257315 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1470134359 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15438,RMVar_hsa_circ_24649,RMVar_hsa_circ_349527,RMVar_hsa_circ_51852,RMVar_hsa_circ_272982,RMVar_hsa_circ_73173,RMVar_hsa_circ_319370,RMVar_hsa_circ_65402,RMVar_hsa_circ_119203,RMVar_hsa_circ_139082,RMVar_hsa_circ_139083,RMVar_hsa_circ_139087,RMVar_hsa_circ_75443,RMVar_hsa_circ_110721,RMVar_hsa_circ_139085,RMVar_hsa_circ_370798,RMVar_hsa_circ_333312,RMVar_hsa_circ_359834,RMVar_hsa_circ_139086,RMVar_hsa_circ_281319 20170 RMVar_ID_20170 Human_SNP_ID_46652040 A-to-I Human chr1 + 203837093 203837093 203837093 GAAGTGGGCAGATCACCTGAGCTCAGGAGTTCAAGACCAGCCTGGGCAACATGGCAAACCCTTGT GAAGTGGGCAGATCACCTGAGCTCAGGAGTTCCAGACCAGCCTGGGCAACATGGCAAACCCTTGT A C ZC3H11A,ZBED6 Ensembl:ENSG00000058673,Ensembl:ENSG00000257315 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1327452232 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15438,RMVar_hsa_circ_24649,RMVar_hsa_circ_349527,RMVar_hsa_circ_51852,RMVar_hsa_circ_272982,RMVar_hsa_circ_73173,RMVar_hsa_circ_319370,RMVar_hsa_circ_65402,RMVar_hsa_circ_119203,RMVar_hsa_circ_139082,RMVar_hsa_circ_139083,RMVar_hsa_circ_139087,RMVar_hsa_circ_75443,RMVar_hsa_circ_110721,RMVar_hsa_circ_139085,RMVar_hsa_circ_370798,RMVar_hsa_circ_333312,RMVar_hsa_circ_359834,RMVar_hsa_circ_139086,RMVar_hsa_circ_281319 20171 RMVar_ID_20171 Human_SNP_ID_46656850 A-to-I Human chr1 + 203855070 203855069 203855071 AGAATAATTCTGCAGGGTGTTTTTTTTAAGACAGAGTCTCACTCTGTTGCCCAGGATAGAATGCA AGAATAATTCTGCAGGGTGTTTTTTTTAAGAC__AGTCTCACTCTGTTGCCCAGGATAGAATGCA CAG C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs756305532 Functional Loss DEL dbSNP153 33..34 33 - - - 20172 RMVar_ID_20172 Human_SNP_ID_46657096 A-to-I Human chr1 + 203856109 203856109 203856109 GGAGAATTGTGTGAACCTGGAAGGCGGAGGTTACAGTGAGCCGAGATCAATCACCACTGCACTCC GGAGAATTGTGTGAACCTGGAAGGCGGAGGTTGCAGTGAGCCGAGATCAATCACCACTGCACTCC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1558153185 Functional Loss SNV dbSNP153 33..33 33 - - - 20173 RMVar_ID_20173 Human_SNP_ID_46659701 A-to-I Human chr1 + 203865587 203865587 203865587 CAAGCAATCAGTTCGGCAGTGGACATCAGCTCAGAGTCGTCAAGTTCAGTTCAGTTCTAACACTA CAAGCAATCAGTTCGGCAGTGGACATCAGCTCGGAGTCGTCAAGTTCAGTTCAGTTCTAACACTA A G SNRPE Ensembl:ENSG00000182004 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6421775 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10732969 GWAS_ID_1745,GWAS_ID_1746,GWAS_ID_1747,GWAS_ID_1748,GWAS_ID_1749,GWAS_ID_1750,GWAS_ID_1751,GWAS_ID_1752,GWAS_ID_1753,GWAS_ID_1754,GWAS_ID_1755,GWAS_ID_1756,GWAS_ID_1757,GWAS_ID_1758,GWAS_ID_1759,GWAS_ID_1760,GWAS_ID_1761,GWAS_ID_1762,GWAS_ID_1763,GWAS_ID_1764,GWAS_ID_1765,GWAS_ID_1766,GWAS_ID_1767,GWAS_ID_1768,GWAS_ID_1769,GWAS_ID_1770,GWAS_ID_1771,GWAS_ID_1772,GWAS_ID_1773,GWAS_ID_1774,GWAS_ID_1775,GWAS_ID_1776,GWAS_ID_1777,GWAS_ID_1778,GWAS_ID_1779,GWAS_ID_1780,GWAS_ID_1781,GWAS_ID_1782,GWAS_ID_1783,GWAS_ID_1784,GWAS_ID_1785,GWAS_ID_1786,GWAS_ID_1787,GWAS_ID_1788,GWAS_ID_1789,GWAS_ID_1790,GWAS_ID_1791,GWAS_ID_1792,GWAS_ID_1793,GWAS_ID_1794,GWAS_ID_1795,GWAS_ID_1796,GWAS_ID_1797,GWAS_ID_1798,GWAS_ID_1799,GWAS_ID_1800,GWAS_ID_1801,GWAS_ID_1802,GWAS_ID_1803,GWAS_ID_1804,GWAS_ID_1805,GWAS_ID_1806,GWAS_ID_1807,GWAS_ID_1808,GWAS_ID_1809,GWAS_ID_1810,GWAS_ID_1811,GWAS_ID_1812,GWAS_ID_1813,GWAS_ID_1814,GWAS_ID_1815,GWAS_ID_1816,GWAS_ID_1817,GWAS_ID_1818,GWAS_ID_1819,GWAS_ID_1820,GWAS_ID_1821,GWAS_ID_1822,GWAS_ID_1823,GWAS_ID_1824,GWAS_ID_1825,GWAS_ID_1826,GWAS_ID_1827,GWAS_ID_1828,GWAS_ID_1829,GWAS_ID_1830,GWAS_ID_1831,GWAS_ID_1832,GWAS_ID_1833,GWAS_ID_1834,GWAS_ID_1835 RMVar_hsa_circ_125662,RMVar_hsa_circ_139094 20174 RMVar_ID_20174 Human_SNP_ID_46659992 A-to-I Human chr1 + 203866710 203866710 203866710 CACTCATCTTTTAAAAACACCAGTCTGAACATATGTCATCCCTTTGCTTGAAATACTGCAATGAC CACTCATCTTTTAAAAACACCAGTCTGAACATGTGTCATCCCTTTGCTTGAAATACTGCAATGAC A G SNRPE Ensembl:ENSG00000182004 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7540013 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10733050,Human_RBP_ID_19255799,Human_RBP_ID_21911128 GWAS_ID_1836,GWAS_ID_1837,GWAS_ID_1838,GWAS_ID_1839,GWAS_ID_1840,GWAS_ID_1841,GWAS_ID_1842,GWAS_ID_1843,GWAS_ID_1844,GWAS_ID_1845,GWAS_ID_1846,GWAS_ID_1847,GWAS_ID_1848,GWAS_ID_1849,GWAS_ID_1850,GWAS_ID_1851,GWAS_ID_1852,GWAS_ID_1853,GWAS_ID_1854,GWAS_ID_1855,GWAS_ID_1856,GWAS_ID_1857,GWAS_ID_1858,GWAS_ID_1859,GWAS_ID_1860,GWAS_ID_1861,GWAS_ID_1862,GWAS_ID_1863,GWAS_ID_1864,GWAS_ID_1865,GWAS_ID_1866,GWAS_ID_1867,GWAS_ID_1868,GWAS_ID_1869,GWAS_ID_1870,GWAS_ID_1871,GWAS_ID_1872,GWAS_ID_1873,GWAS_ID_1874,GWAS_ID_1875,GWAS_ID_1876,GWAS_ID_1877,GWAS_ID_1878,GWAS_ID_1879,GWAS_ID_1880,GWAS_ID_1881,GWAS_ID_1882,GWAS_ID_1883,GWAS_ID_1884,GWAS_ID_1885,GWAS_ID_1886,GWAS_ID_1887,GWAS_ID_1888,GWAS_ID_1889,GWAS_ID_1890,GWAS_ID_1891,GWAS_ID_1892,GWAS_ID_1893,GWAS_ID_1894,GWAS_ID_1895,GWAS_ID_1896,GWAS_ID_1897,GWAS_ID_1898,GWAS_ID_1899,GWAS_ID_1900,GWAS_ID_1901,GWAS_ID_1902,GWAS_ID_1903,GWAS_ID_1904,GWAS_ID_1905,GWAS_ID_1906,GWAS_ID_1907,GWAS_ID_1908,GWAS_ID_1909,GWAS_ID_1910,GWAS_ID_1911,GWAS_ID_1912,GWAS_ID_1913,GWAS_ID_1914,GWAS_ID_1915,GWAS_ID_1916,GWAS_ID_1917,GWAS_ID_1918,GWAS_ID_1919,GWAS_ID_1920,GWAS_ID_1921,GWAS_ID_1922,GWAS_ID_1923,GWAS_ID_1924,GWAS_ID_1925,GWAS_ID_1926 RMVar_hsa_circ_125662,RMVar_hsa_circ_139094 20175 RMVar_ID_20175 Human_SNP_ID_46660482 A-to-I Human chr1 + 203868236 203868236 203868236 TACCACCACGCCTGGCTGATTTTTTGTGTTTTAGTAGAGACGGGGTTTCACTGTGTTGCCCAGGC TACCACCACGCCTGGCTGATTTTTTGTGTTTTGGTAGAGACGGGGTTTCACTGTGTTGCCCAGGC A G SNRPE Ensembl:ENSG00000182004 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs547302411 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10733101,Human_RBP_ID_24624836 RMVar_hsa_circ_125662,RMVar_hsa_circ_139094 20176 RMVar_ID_20176 Human_SNP_ID_46660499 A-to-I Human chr1 + 203868294 203868294 203868294 CCCAGGCTGGTCTCTAACTTCTGAGCTCAGGCAATCCACCTGCCTCGGCCTCCCAAATGCTGGGA CCCAGGCTGGTCTCTAACTTCTGAGCTCAGGCGATCCACCTGCCTCGGCCTCCCAAATGCTGGGA A G SNRPE Ensembl:ENSG00000182004 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs978322518 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125662,RMVar_hsa_circ_139094 20177 RMVar_ID_20177 Human_SNP_ID_46717741 A-to-I Human chr1 + 204097998 204097998 204097998 CTCTCATCTCAGCCTCCTTAGTAGCTGGGACTACAGGTGTGTGCCACCACACCTGGCTAATTTTT CTCTCATCTCAGCCTCCTTAGTAGCTGGGACTGCAGGTGTGTGCCACCACACCTGGCTAATTTTT A G SOX13 Ensembl:ENSG00000143842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1040110258 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121804,RMVar_hsa_circ_139095 20178 RMVar_ID_20178 Human_SNP_ID_46717764 A-to-I Human chr1 + 204098122 204098122 204098122 AACTCAAGCAATCCACCCACCTCGACCTTCCAAAGTGCTGGGATTACAGATGTGAGTCACCATCG AACTCAAGCAATCCACCCACCTCGACCTTCCAGAGTGCTGGGATTACAGATGTGAGTCACCATCG A G SOX13 Ensembl:ENSG00000143842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs562397480 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121804,RMVar_hsa_circ_139095 20179 RMVar_ID_20179 Human_SNP_ID_46720912 A-to-I Human chr1 + 204111779 204111779 204111779 GTTGTCCAGACTGGCCTCAAACACCTGACCTCAAGTGATGTGCCTTCCTCAGCCTCTTGAGTAAC GTTGTCCAGACTGGCCTCAAACACCTGACCTCTAGTGATGTGCCTTCCTCAGCCTCTTGAGTAAC A T SOX13 Ensembl:ENSG00000143842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1024523371 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121804,RMVar_hsa_circ_139095 20180 RMVar_ID_20180 Human_SNP_ID_46722688 A-to-I Human chr1 + 204118193 204118193 204118193 CCTGTAGTCCCAGCTACTCAGAAGACTGAGGCAGGAGAATCGCTTGAACCTGGGAGGTGGAGGTT CCTGTAGTCCCAGCTACTCAGAAGACTGAGGCCGGAGAATCGCTTGAACCTGGGAGGTGGAGGTT A C SOX13 Ensembl:ENSG00000143842 Protein coding exon GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1232935353 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17781,RMVar_hsa_circ_304930,RMVar_hsa_circ_318907,RMVar_hsa_circ_139096,RMVar_hsa_circ_139097,RMVar_hsa_circ_53476,RMVar_hsa_circ_74284 20181 RMVar_ID_20181 Human_SNP_ID_46755895 A-to-I Human chr1 - 204248322 204248322 204248322 TGGAGAAACCCTGTCTCTACTAAAAATACAAAATTAGCCGGTTGTGGTGGCACACACCTGTAGTC TGGAGAAACCCTGTCTCTACTAAAAATACAAAGTTAGCCGGTTGTGGTGGCACACACCTGTAGTC T C PLEKHA6 Ensembl:ENSG00000143850 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs910107437 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43324,RMVar_hsa_circ_139118,RMVar_hsa_circ_94837,RMVar_hsa_circ_113458,RMVar_hsa_circ_83920,RMVar_hsa_circ_139120,RMVar_hsa_circ_139122,RMVar_hsa_circ_78050,RMVar_hsa_circ_139121,RMVar_hsa_circ_139119,RMVar_hsa_circ_69473,RMVar_hsa_circ_66610,RMVar_hsa_circ_56909,RMVar_hsa_circ_66325,RMVar_hsa_circ_353944,RMVar_hsa_circ_61923 20182 RMVar_ID_20182 Human_SNP_ID_46791221 A-to-I Human chr1 - 204400080 204400080 204400080 GGTGTGCACCACTTTGCTCACCTATTTTTTGTAGAGACAGGGTCTCACTATGTTGCCCGGGCTGG GGTGTGCACCACTTTGCTCACCTATTTTTTGTGGAGACAGGGTCTCACTATGTTGCCCGGGCTGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1007387311 Functional Loss SNV dbSNP153 33..33 33 - - - 20183 RMVar_ID_20183 Human_SNP_ID_46791251 A-to-I Human chr1 - 204400201 204400201 204400201 ACAGTGTCTCACTGTCACCCAGGCTCTGAAGTACAGTGGCATGATCACAGCTCACTGCAGCCTCG ACAGTGTCTCACTGTCACCCAGGCTCTGAAGTGCAGTGGCATGATCACAGCTCACTGCAGCCTCG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1226808092 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10735138,Human_RBP_ID_19256310,Human_RBP_ID_22781796 20184 RMVar_ID_20184 Human_SNP_ID_46791801 A-to-I Human chr1 - 204402500 204402500 204402500 GGGAGGCTGAGACAGGAGGGTTGCTTGAGCACAGAAGTTCAAGCCTGCAGTGAGCTGTGATTCCA GGGAGGCTGAGACAGGAGGGTTGCTTGAGCACGGAAGTTCAAGCCTGCAGTGAGCTGTGATTCCA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1287779069 Functional Loss SNV dbSNP153 33..33 33 - - - 20185 RMVar_ID_20185 Human_SNP_ID_46792149 A-to-I Human chr1 - 204403864 204403864 204403864 TAAGAGTTCTTCCATATACTAGCCTCCTTGGAAGAAGTGATCAGAAGGTGATAAGAAGGACAGAA TAAGAGTTCTTCCATATACTAGCCTCCTTGGAGGAAGTGATCAGAAGGTGATAAGAAGGACAGAA T C PPP1R15B Ensembl:ENSG00000158615 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs552370960 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1419169,Human_RBP_ID_1733646,Human_RBP_ID_8295557,Human_RBP_ID_8741057,Human_RBP_ID_10735286,Human_RBP_ID_18222395,Human_RBP_ID_22486778,Human_RBP_ID_26801442 20186 RMVar_ID_20186 Human_SNP_ID_46794909 A-to-I Human chr1 + 204413015 204413015 204413015 CGTGAGCCACCGTGCTCGGCCAATTTTTGCATATTTTTATAGAGACAGGGTTTCGTCGTGTTGCC CGTGAGCCACCGTGCTCGGCCAATTTTTGCATGTTTTTATAGAGACAGGGTTTCGTCGTGTTGCC A G AL606489.1 Ensembl:ENSG00000226330 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1029359079 Functional Loss SNV dbSNP153 33..33 33 - - - 20187 RMVar_ID_20187 Human_SNP_ID_46794910 A-to-I Human chr1 + 204413015 204413015 204413015 CGTGAGCCACCGTGCTCGGCCAATTTTTGCATATTTTTATAGAGACAGGGTTTCGTCGTGTTGCC CGTGAGCCACCGTGCTCGGCCAATTTTTGCATTTTTTTATAGAGACAGGGTTTCGTCGTGTTGCC A T AL606489.1 Ensembl:ENSG00000226330 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1029359079 Functional Loss SNV dbSNP153 33..33 33 - - - 20188 RMVar_ID_20188 Human_SNP_ID_46797106 A-to-I Human chr1 - 204422318 204422318 204422318 AAAGTAATTTTTAGTAGAGCCAAGGTCTTGCTACATTGCGCAGGCTGGTCTTGAATTCCTGAGTC AAAGTAATTTTTAGTAGAGCCAAGGTCTTGCTGCATTGCGCAGGCTGGTCTTGAATTCCTGAGTC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1177518764 Functional Loss SNV dbSNP153 33..33 33 - - - 20189 RMVar_ID_20189 Human_SNP_ID_46798686 A-to-I Human chr1 - 204428631 204428631 204428631 AAATTAGCTGGGCGTGGTGGCGCAGGCCTGTAATCTCATCTACTTGGGAGCCTGAGGTTGCAGTG AAATTAGCTGGGCGTGGTGGCGCAGGCCTGTAGTCTCATCTACTTGGGAGCCTGAGGTTGCAGTG T C PIK3C2B Ensembl:ENSG00000133056 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1000531643 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10735822 RMVar_hsa_circ_22835,RMVar_hsa_circ_139129,RMVar_hsa_circ_100337,RMVar_hsa_circ_319406,RMVar_hsa_circ_101510,RMVar_hsa_circ_139130,RMVar_hsa_circ_139131 20190 RMVar_ID_20190 Human_SNP_ID_46798802 A-to-I Human chr1 - 204429088 204429088 204429088 GAGTAGCTGGGACTGTAGGCATGGGCCACCACACCCGGCTAATTTTTGTATTTTTTTTTTTGTAA GAGTAGCTGGGACTGTAGGCATGGGCCACCACCCCCGGCTAATTTTTGTATTTTTTTTTTTGTAA T G PIK3C2B Ensembl:ENSG00000133056 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1369660010 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22835,RMVar_hsa_circ_139129,RMVar_hsa_circ_100337,RMVar_hsa_circ_319406,RMVar_hsa_circ_101510,RMVar_hsa_circ_139130,RMVar_hsa_circ_139131 20191 RMVar_ID_20191 Human_SNP_ID_46803420 A-to-I Human chr1 - 204448238 204448238 204448238 TGGTGGCGGGTGCCTGTAAATCCCAGGTACTCAGGAAGCTGAGGCATGAGAACCACTTGAACCGG TGGTGGCGGGTGCCTGTAAATCCCAGGTACTCGGGAAGCTGAGGCATGAGAACCACTTGAACCGG T C PIK3C2B Ensembl:ENSG00000133056 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1254222221 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88342,RMVar_hsa_circ_101510,RMVar_hsa_circ_139131,RMVar_hsa_circ_6041,RMVar_hsa_circ_61272,RMVar_hsa_circ_139134,RMVar_hsa_circ_265937,RMVar_hsa_circ_9781,RMVar_hsa_circ_118320,RMVar_hsa_circ_139139 20192 RMVar_ID_20192 Human_SNP_ID_46803448 A-to-I Human chr1 - 204448374 204448374 204448374 AATGAGGCTGGGTGTGGTGGCTCATGCCTGCAATCCCAGCACTTTGGGAGGCTGAGGCAGGGGGA AATGAGGCTGGGTGTGGTGGCTCATGCCTGCAGTCCCAGCACTTTGGGAGGCTGAGGCAGGGGGA T C PIK3C2B Ensembl:ENSG00000133056 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs907672177 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88342,RMVar_hsa_circ_101510,RMVar_hsa_circ_139131,RMVar_hsa_circ_6041,RMVar_hsa_circ_61272,RMVar_hsa_circ_139134,RMVar_hsa_circ_265937,RMVar_hsa_circ_9781,RMVar_hsa_circ_118320,RMVar_hsa_circ_139139 20193 RMVar_ID_20193 Human_SNP_ID_46804742 A-to-I Human chr1 - 204453403 204453403 204453403 AAATATAAATATGAAACCAAAAGCACAAGGTAATATTAATCACCACATGTAAACAATAATTTGGT AAATATAAATATGAAACCAAAAGCACAAGGTAGTATTAATCACCACATGTAAACAATAATTTGGT T C PIK3C2B Ensembl:ENSG00000133056 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs3014597 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_1927,GWAS_ID_1928,GWAS_ID_1929 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_37088 20194 RMVar_ID_20194 Human_SNP_ID_46804878 A-to-I Human chr1 - 204453957 204453957 204453957 CAGCCTGACCAACATGGAGAAACCTCGTCTCTACTAAAAAAAATACAAAATAGCCGGGCATGGTG CAGCCTGACCAACATGGAGAAACCTCGTCTCTGCTAAAAAAAATACAAAATAGCCGGGCATGGTG T C PIK3C2B Ensembl:ENSG00000133056 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs996276018 Functional Loss SNV dbSNP153 33..33 33 - - - 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_37088 20195 RMVar_ID_20195 Human_SNP_ID_46804974 A-to-I Human chr1 - 204454293 204454293 204454293 TATTTTTAGCAGAGATGGGGTTTCCATGTGTTAGCTAGGATAGTCTCGATCTCCTGACCTCGTGA TATTTTTAGCAGAGATGGGGTTTCCATGTGTTGGCTAGGATAGTCTCGATCTCCTGACCTCGTGA T C PIK3C2B Ensembl:ENSG00000133056 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1040269221 Functional Loss SNV dbSNP153 33..33 33 - - - 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_37088 20196 RMVar_ID_20196 Human_SNP_ID_46805028 A-to-I Human chr1 - 204454455 204454455 204454455 TTTTTTGAGAGGCAGCCTCGCTTTGTTGCCCAAGCTGGAGTGCAGTGGTGCGATCTCGGCTCACT TTTTTTGAGAGGCAGCCTCGCTTTGTTGCCCAGGCTGGAGTGCAGTGGTGCGATCTCGGCTCACT T C PIK3C2B Ensembl:ENSG00000133056 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs893074689 Functional Loss SNV dbSNP153 33..33 33 - - - 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_37088 20197 RMVar_ID_20197 Human_SNP_ID_46809095 A-to-I Human chr1 - 204468971 204468971 204468971 AAGACACCTCTGGAAAACCCGTGGCCAGGAGCAAGACTATGCCCCCTCAGGTGCCCCCCCGCACC AAGACACCTCTGGAAAACCCGTGGCCAGGAGCCAGACTATGCCCCCTCAGGTGCCCCCCCGCACC T G PIK3C2B Ensembl:ENSG00000133056 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1427439279 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19921 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 20198 RMVar_ID_20198 Human_SNP_ID_46810094 A-to-I Human chr1 - 204472773 204472773 204472773 TCAGGCTTCAGTACTTTGTTTTTTTTAGACAGAGTTTTGGTCTTGTTGCCCAAGCTGGAGTGAAA TCAGGCTTCAGTACTTTGTTTTTTTTAGACAGGGTTTTGGTCTTGTTGCCCAAGCTGGAGTGAAA T C PIK3C2B Ensembl:ENSG00000133056 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1379783757 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23990,RMVar_hsa_circ_88342,RMVar_hsa_circ_139134 20199 RMVar_ID_20199 Human_SNP_ID_46810877 A-to-I Human chr1 - 204476327 204476327 204476327 GCTCAAGCAATCCCCCCGCCTCGGCTTCCCAAAGTCCTTGGGATTACAGACATGAGCCACCACGC GCTCAAGCAATCCCCCCGCCTCGGCTTCCCAAGGTCCTTGGGATTACAGACATGAGCCACCACGC T C PIK3C2B Ensembl:ENSG00000133056 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232997190 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23990,RMVar_hsa_circ_88342,RMVar_hsa_circ_139134 20200 RMVar_ID_20200 Human_SNP_ID_46813573 A-to-I Human chr1 - 204487184 204487184 204487184 GGAGGATCACTTGACCTGGGGAGTTTGAGGTTACAGTAAGCTATGATTGCACCACTGCACTCCAG GGAGGATCACTTGACCTGGGGAGTTTGAGGTTGCAGTAAGCTATGATTGCACCACTGCACTCCAG T C PIK3C2B Ensembl:ENSG00000133056 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs890356670 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23990,RMVar_hsa_circ_88342,RMVar_hsa_circ_139134 20201 RMVar_ID_20201 Human_SNP_ID_46821971 A-to-I Human chr1 + 204518831 204518831 204518831 GGATTACAGGCGTTGTGCCACCACGCCCAGCTAATTTTTGTATTTTCAGTAGAGAGAGGTTTTCA GGATTACAGGCGTTGTGCCACCACGCCCAGCTGATTTTTGTATTTTCAGTAGAGAGAGGTTTTCA A G MDM4 Ensembl:ENSG00000198625 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223106345 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139147,RMVar_hsa_circ_123815 20202 RMVar_ID_20202 Human_SNP_ID_46822880 A-to-I Human chr1 + 204522207 204522203 204522208 TAAATTAGCTGGGCATGGTGGCATGCACCTGTAGTCCCAACTACTTGGGAGGCTGAGGTGGGAGG TAAATTAGCTGGGCATGGTGGCATGCACC_____TCCCAACTACTTGGGAGGCTGAGGTGGGAGG CTGTAG C MDM4 Ensembl:ENSG00000198625 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1408653681 Functional Loss DEL dbSNP153 30..34 33 - - - RMVar_hsa_circ_139147,RMVar_hsa_circ_123815 20203 RMVar_ID_20203 Human_SNP_ID_46822882 A-to-I Human chr1 + 204522207 204522207 204522207 TAAATTAGCTGGGCATGGTGGCATGCACCTGTAGTCCCAACTACTTGGGAGGCTGAGGTGGGAGG TAAATTAGCTGGGCATGGTGGCATGCACCTGTCGTCCCAACTACTTGGGAGGCTGAGGTGGGAGG A C MDM4 Ensembl:ENSG00000198625 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs949854112 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139147,RMVar_hsa_circ_123815 20204 RMVar_ID_20204 Human_SNP_ID_46823351 A-to-I Human chr1 + 204523613 204523613 204523613 TCAGGTGATTCTCATGCCTCAGCTTCCTTAGTAGTTGGGACTGCAGGCTCGTGCCATGCCCAGCT TCAGGTGATTCTCATGCCTCAGCTTCCTTAGTGGTTGGGACTGCAGGCTCGTGCCATGCCCAGCT A G MDM4 Ensembl:ENSG00000198625 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs995731638 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10736158 RMVar_hsa_circ_139147,RMVar_hsa_circ_123815 20205 RMVar_ID_20205 Human_SNP_ID_46824401 A-to-I Human chr1 + 204527148 204527148 204527148 GAAACCCTGTCTCTAAAAAAAAAAAAAAAAATACAAAAATTGGGCGGGCATGGTGGTCTGCTCGT GAAACCCTGTCTCTAAAAAAAAAAAAAAAAATGCAAAAATTGGGCGGGCATGGTGGTCTGCTCGT A G MDM4 Ensembl:ENSG00000198625 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054883846 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118234,RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_367720,RMVar_hsa_circ_284316,RMVar_hsa_circ_22678,RMVar_hsa_circ_89387,RMVar_hsa_circ_139149,RMVar_hsa_circ_92157,RMVar_hsa_circ_139150,RMVar_hsa_circ_139148,RMVar_hsa_circ_348206,RMVar_hsa_circ_79149,RMVar_hsa_circ_139152,RMVar_hsa_circ_139153 20206 RMVar_ID_20206 Human_SNP_ID_46824425 A-to-I Human chr1 + 204527232 204527232 204527232 GGGAGGCTGAAGTGGGAGGATCGCTTGAACCCAGAAGGTGAAGGTTGCAATGAGGTGCACTCCAG GGGAGGCTGAAGTGGGAGGATCGCTTGAACCCGGAAGGTGAAGGTTGCAATGAGGTGCACTCCAG A G MDM4 Ensembl:ENSG00000198625 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1284359419 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5338824,Human_RBP_ID_18508813 RMVar_hsa_circ_118234,RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_367720,RMVar_hsa_circ_284316,RMVar_hsa_circ_22678,RMVar_hsa_circ_89387,RMVar_hsa_circ_139149,RMVar_hsa_circ_92157,RMVar_hsa_circ_139150,RMVar_hsa_circ_139148,RMVar_hsa_circ_348206,RMVar_hsa_circ_79149,RMVar_hsa_circ_139152,RMVar_hsa_circ_139153 20207 RMVar_ID_20207 Human_SNP_ID_46826328 A-to-I Human chr1 + 204534600 204534600 204534600 ACCTCCGCCTCCGTGGCACAAGCAGTCCTCCCACCTCAGCCTCCTCAGTAGCTGGGACTACAGGA ACCTCCGCCTCCGTGGCACAAGCAGTCCTCCCCCCTCAGCCTCCTCAGTAGCTGGGACTACAGGA A C MDM4 Ensembl:ENSG00000198625 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1357437831 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10736443 RMVar_hsa_circ_118234,RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_22678,RMVar_hsa_circ_89387,RMVar_hsa_circ_139149,RMVar_hsa_circ_92157,RMVar_hsa_circ_139148,RMVar_hsa_circ_47157,RMVar_hsa_circ_139153,RMVar_hsa_circ_336799,RMVar_hsa_circ_83671,RMVar_hsa_circ_139155,RMVar_hsa_circ_139156,RMVar_hsa_circ_139157,RMVar_hsa_circ_119956,RMVar_hsa_circ_364680 20208 RMVar_ID_20208 Human_SNP_ID_46826332 A-to-I Human chr1 + 204534617 204534617 204534617 ACAAGCAGTCCTCCCACCTCAGCCTCCTCAGTAGCTGGGACTACAGGAGTATGCCACCACACCTG ACAAGCAGTCCTCCCACCTCAGCCTCCTCAGTGGCTGGGACTACAGGAGTATGCCACCACACCTG A G MDM4 Ensembl:ENSG00000198625 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1349351193 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118234,RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_22678,RMVar_hsa_circ_89387,RMVar_hsa_circ_139149,RMVar_hsa_circ_92157,RMVar_hsa_circ_139148,RMVar_hsa_circ_47157,RMVar_hsa_circ_139153,RMVar_hsa_circ_336799,RMVar_hsa_circ_83671,RMVar_hsa_circ_139155,RMVar_hsa_circ_139156,RMVar_hsa_circ_139157,RMVar_hsa_circ_119956,RMVar_hsa_circ_364680 20209 RMVar_ID_20209 Human_SNP_ID_46826604 A-to-I Human chr1 + 204535608 204535608 204535608 TAGGCTGGAGTGCAGTGGTGCGATCTCGGCTCACTGCAACCTCTGCCTCCTGGGTTCAGGTGATC TAGGCTGGAGTGCAGTGGTGCGATCTCGGCTCGCTGCAACCTCTGCCTCCTGGGTTCAGGTGATC A G MDM4 Ensembl:ENSG00000198625 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs556056925 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118234,RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_22678,RMVar_hsa_circ_89387,RMVar_hsa_circ_139149,RMVar_hsa_circ_92157,RMVar_hsa_circ_139148,RMVar_hsa_circ_47157,RMVar_hsa_circ_139153,RMVar_hsa_circ_336799,RMVar_hsa_circ_83671,RMVar_hsa_circ_139155,RMVar_hsa_circ_139156,RMVar_hsa_circ_139157,RMVar_hsa_circ_119956,RMVar_hsa_circ_364680 20210 RMVar_ID_20210 Human_SNP_ID_46826637 A-to-I Human chr1 + 204535713 204535713 204535713 CACCACCAAGCCCGGCTAATTTTTGTGATTTTAGTAGAGATGAGGTTTCACCAGGCTGGTGGGTT CACCACCAAGCCCGGCTAATTTTTGTGATTTTGGTAGAGATGAGGTTTCACCAGGCTGGTGGGTT A G MDM4 Ensembl:ENSG00000198625 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1420875920 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10736493,Human_RBP_ID_23303913,Human_RBP_ID_23357426,Human_RBP_ID_24625140 RMVar_hsa_circ_118234,RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_22678,RMVar_hsa_circ_89387,RMVar_hsa_circ_139149,RMVar_hsa_circ_92157,RMVar_hsa_circ_139148,RMVar_hsa_circ_47157,RMVar_hsa_circ_139153,RMVar_hsa_circ_336799,RMVar_hsa_circ_83671,RMVar_hsa_circ_139155,RMVar_hsa_circ_139156,RMVar_hsa_circ_139157,RMVar_hsa_circ_119956,RMVar_hsa_circ_364680 20211 RMVar_ID_20211 Human_SNP_ID_46826720 A-to-I Human chr1 + 204536044 204536044 204536044 AGCACTTTGGGAGGCCGAGGCGGGTGGATCACAAAGTCAGGAGTTTGAGACCAGCCTGGCCAAGA AGCACTTTGGGAGGCCGAGGCGGGTGGATCACGAAGTCAGGAGTTTGAGACCAGCCTGGCCAAGA A G MDM4 Ensembl:ENSG00000198625 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1402649963 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118234,RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_22678,RMVar_hsa_circ_89387,RMVar_hsa_circ_139149,RMVar_hsa_circ_92157,RMVar_hsa_circ_139148,RMVar_hsa_circ_47157,RMVar_hsa_circ_139153,RMVar_hsa_circ_336799,RMVar_hsa_circ_83671,RMVar_hsa_circ_139155,RMVar_hsa_circ_139156,RMVar_hsa_circ_139157,RMVar_hsa_circ_119956,RMVar_hsa_circ_364680 20212 RMVar_ID_20212 Human_SNP_ID_46826721 A-to-I Human chr1 + 204536045 204536045 204536045 GCACTTTGGGAGGCCGAGGCGGGTGGATCACAAAGTCAGGAGTTTGAGACCAGCCTGGCCAAGAT GCACTTTGGGAGGCCGAGGCGGGTGGATCACAGAGTCAGGAGTTTGAGACCAGCCTGGCCAAGAT A G MDM4 Ensembl:ENSG00000198625 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs570875588 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118234,RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_22678,RMVar_hsa_circ_89387,RMVar_hsa_circ_139149,RMVar_hsa_circ_92157,RMVar_hsa_circ_139148,RMVar_hsa_circ_47157,RMVar_hsa_circ_139153,RMVar_hsa_circ_336799,RMVar_hsa_circ_83671,RMVar_hsa_circ_139155,RMVar_hsa_circ_139156,RMVar_hsa_circ_139157,RMVar_hsa_circ_119956,RMVar_hsa_circ_364680 20213 RMVar_ID_20213 Human_SNP_ID_46826746 A-to-I Human chr1 + 204536129 204536129 204536129 TAAAAATACAAAAATTAGTCAGGCGTGCGCCTATAATCCTAGCTACTTGGGAGGCTGAGGCAGGA TAAAAATACAAAAATTAGTCAGGCGTGCGCCTGTAATCCTAGCTACTTGGGAGGCTGAGGCAGGA A G MDM4 Ensembl:ENSG00000198625 Protein coding intron GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs1220490302 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118234,RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_22678,RMVar_hsa_circ_89387,RMVar_hsa_circ_139149,RMVar_hsa_circ_92157,RMVar_hsa_circ_139148,RMVar_hsa_circ_47157,RMVar_hsa_circ_139153,RMVar_hsa_circ_336799,RMVar_hsa_circ_83671,RMVar_hsa_circ_139155,RMVar_hsa_circ_139156,RMVar_hsa_circ_139157,RMVar_hsa_circ_119956,RMVar_hsa_circ_364680 20214 RMVar_ID_20214 Human_SNP_ID_46826747 A-to-I Human chr1 + 204536131 204536130 204536131 AAAATACAAAAATTAGTCAGGCGTGCGCCTATAATCCTAGCTACTTGGGAGGCTGAGGCAGGAGA AAAATACAAAAATTAGTCAGGCGTGCGCCTAT_ATCCTAGCTACTTGGGAGGCTGAGGCAGGAGA TA T MDM4 Ensembl:ENSG00000198625 Protein coding intron GSE47997;GSE38233;GSE38233;GSE100210;GSE100210 K562 cells&HepG2 cells;cultured B-cells;cultured B-cells;HepG2 cell line;HepG2 cell line - 23474544,24183664,24183664,29129909,29129909 RNA-Seq:(High) rs1234698842 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_118234,RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_22678,RMVar_hsa_circ_89387,RMVar_hsa_circ_139149,RMVar_hsa_circ_92157,RMVar_hsa_circ_139148,RMVar_hsa_circ_47157,RMVar_hsa_circ_139153,RMVar_hsa_circ_336799,RMVar_hsa_circ_83671,RMVar_hsa_circ_139155,RMVar_hsa_circ_139156,RMVar_hsa_circ_139157,RMVar_hsa_circ_119956,RMVar_hsa_circ_364680 20215 RMVar_ID_20215 Human_SNP_ID_46826753 A-to-I Human chr1 + 204536158 204536158 204536158 CCTATAATCCTAGCTACTTGGGAGGCTGAGGCAGGAGAATCACTTGAGCCAGGGAGGTAGAGGTT CCTATAATCCTAGCTACTTGGGAGGCTGAGGCTGGAGAATCACTTGAGCCAGGGAGGTAGAGGTT A T MDM4 Ensembl:ENSG00000198625 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1446882970 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10736523 RMVar_hsa_circ_118234,RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_22678,RMVar_hsa_circ_89387,RMVar_hsa_circ_139149,RMVar_hsa_circ_92157,RMVar_hsa_circ_139148,RMVar_hsa_circ_47157,RMVar_hsa_circ_139153,RMVar_hsa_circ_336799,RMVar_hsa_circ_83671,RMVar_hsa_circ_139155,RMVar_hsa_circ_139156,RMVar_hsa_circ_139157,RMVar_hsa_circ_119956,RMVar_hsa_circ_364680 20216 RMVar_ID_20216 Human_SNP_ID_46826759 A-to-I Human chr1 + 204536184 204536184 204536184 TGAGGCAGGAGAATCACTTGAGCCAGGGAGGTAGAGGTTTTAGTGAGCCGAGATTGCGCCACTGC TGAGGCAGGAGAATCACTTGAGCCAGGGAGGTGGAGGTTTTAGTGAGCCGAGATTGCGCCACTGC A G MDM4 Ensembl:ENSG00000198625 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1025594283 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10736524,Human_RBP_ID_17557401 RMVar_hsa_circ_118234,RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_22678,RMVar_hsa_circ_89387,RMVar_hsa_circ_139149,RMVar_hsa_circ_92157,RMVar_hsa_circ_139148,RMVar_hsa_circ_47157,RMVar_hsa_circ_139153,RMVar_hsa_circ_336799,RMVar_hsa_circ_83671,RMVar_hsa_circ_139155,RMVar_hsa_circ_139156,RMVar_hsa_circ_139157,RMVar_hsa_circ_119956,RMVar_hsa_circ_364680 20217 RMVar_ID_20217 Human_SNP_ID_46830460 A-to-I Human chr1 + 204550605 204550605 204550605 TTTTTTTGAGAGACGGTCTCACTTTGTCATCCAAGCTGGAGTGCAGTGGTGCAAACACGGCCCAC TTTTTTTGAGAGACGGTCTCACTTTGTCATCCTAGCTGGAGTGCAGTGGTGCAAACACGGCCCAC A T MDM4 Ensembl:ENSG00000198625 Protein coding 3'UTR GSE100210;GSE107867 HepG2 cell line;ASD brains,temporal_cortex - 29129909,30559470 RNA-Seq:(High) rs1242240451 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_744411,Human_RBP_ID_5742510,Human_RBP_ID_10737030,Human_RBP_ID_26850680 Human_miRNA_ID_1269053 RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_89387,RMVar_hsa_circ_92157,RMVar_hsa_circ_139148,RMVar_hsa_circ_139153,RMVar_hsa_circ_83671,RMVar_hsa_circ_139156,RMVar_hsa_circ_139157,RMVar_hsa_circ_119956,RMVar_hsa_circ_88043,RMVar_hsa_circ_91682,RMVar_hsa_circ_139158,RMVar_hsa_circ_139159 20218 RMVar_ID_20218 Human_SNP_ID_46830605 A-to-I Human chr1 + 204551146 204551146 204551146 TTCACTGCAGCCTCGACCTCCCAGATCCAAGCAATCCTCCCACCTAAGCCTCCCAAGTAGCTGGG TTCACTGCAGCCTCGACCTCCCAGATCCAAGCCATCCTCCCACCTAAGCCTCCCAAGTAGCTGGG A C MDM4 Ensembl:ENSG00000198625 Protein coding 3'UTR GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;ASD brains,temporal_cortex;Bronchiolar epithelium,BEP2D cell line - 29129909,30559470,31158229 RNA-Seq:(High) rs1436505028 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223146,Human_RBP_ID_5742533,Human_RBP_ID_10737070,Human_RBP_ID_27392916 RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_89387,RMVar_hsa_circ_92157,RMVar_hsa_circ_139148,RMVar_hsa_circ_139153,RMVar_hsa_circ_83671,RMVar_hsa_circ_139156,RMVar_hsa_circ_139157,RMVar_hsa_circ_119956,RMVar_hsa_circ_88043,RMVar_hsa_circ_91682,RMVar_hsa_circ_139158,RMVar_hsa_circ_139159 20219 RMVar_ID_20219 Human_SNP_ID_46830609 A-to-I Human chr1 + 204551168 204551156 204551169 AGATCCAAGCAATCCTCCCACCTAAGCCTCCCAAGTAGCTGGGTCTATAGGCGCGTGCCACCACC AGATCCAAGCAATCCTCCCAC_____________GTAGCTGGGTCTATAGGCGCGTGCCACCACC CCTAAGCCTCCCAA C MDM4 Ensembl:ENSG00000198625 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs756024307 Functional Loss DEL dbSNP153 22..34 33 - - - Human_RBP_ID_5742533,Human_RBP_ID_10737071 RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_89387,RMVar_hsa_circ_92157,RMVar_hsa_circ_139148,RMVar_hsa_circ_139153,RMVar_hsa_circ_83671,RMVar_hsa_circ_139156,RMVar_hsa_circ_139157,RMVar_hsa_circ_119956,RMVar_hsa_circ_88043,RMVar_hsa_circ_91682,RMVar_hsa_circ_139158,RMVar_hsa_circ_139159 20220 RMVar_ID_20220 Human_SNP_ID_46830651 A-to-I Human chr1 + 204551314 204551314 204551314 GCAACCCTCCTGCCTCAGCCTCTCAAAGTGCTAGGATTGCAGTCCTGAGCTACTGCCCCCTACCC GCAACCCTCCTGCCTCAGCCTCTCAAAGTGCTGGGATTGCAGTCCTGAGCTACTGCCCCCTACCC A G MDM4 Ensembl:ENSG00000198625 Protein coding 3'UTR GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;ASD brains,temporal_cortex;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,30559470,31158229,32596459 RNA-Seq:(High) rs960811539 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_338665,Human_RBP_ID_5742536,Human_RBP_ID_10737082 RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_89387,RMVar_hsa_circ_92157,RMVar_hsa_circ_139148,RMVar_hsa_circ_139153,RMVar_hsa_circ_83671,RMVar_hsa_circ_139156,RMVar_hsa_circ_139157,RMVar_hsa_circ_119956,RMVar_hsa_circ_88043,RMVar_hsa_circ_91682,RMVar_hsa_circ_139158,RMVar_hsa_circ_139159 20221 RMVar_ID_20221 Human_SNP_ID_46830902 A-to-I Human chr1 + 204552111 204552109 204552111 CTGACCGACATGGAGAAACCCCATTTTTACTAAAAATACAAAAAATTAGCTGGGCATGGTGGTGC CTGACCGACATGGAGAAACCCCATTTTTACT__AAATACAAAAAATTAGCTGGGCATGGTGGTGC TAA T MDM4 Ensembl:ENSG00000198625 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1323953376 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_89387,RMVar_hsa_circ_92157,RMVar_hsa_circ_139148,RMVar_hsa_circ_139153,RMVar_hsa_circ_83671,RMVar_hsa_circ_139156,RMVar_hsa_circ_139157,RMVar_hsa_circ_119956,RMVar_hsa_circ_88043,RMVar_hsa_circ_91682,RMVar_hsa_circ_139158,RMVar_hsa_circ_139159 20222 RMVar_ID_20222 Human_SNP_ID_46830906 A-to-I Human chr1 + 204552122 204552122 204552122 GGAGAAACCCCATTTTTACTAAAAATACAAAAAATTAGCTGGGCATGGTGGTGCATGCCTGTAGT GGAGAAACCCCATTTTTACTAAAAATACAAAAGATTAGCTGGGCATGGTGGTGCATGCCTGTAGT A G MDM4 Ensembl:ENSG00000198625 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1211068338 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_89387,RMVar_hsa_circ_92157,RMVar_hsa_circ_139148,RMVar_hsa_circ_139153,RMVar_hsa_circ_83671,RMVar_hsa_circ_139156,RMVar_hsa_circ_139157,RMVar_hsa_circ_119956,RMVar_hsa_circ_88043,RMVar_hsa_circ_91682,RMVar_hsa_circ_139158,RMVar_hsa_circ_139159 20223 RMVar_ID_20223 Human_SNP_ID_46830918 A-to-I Human chr1 + 204552166 204552166 204552166 ATGGTGGTGCATGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACCTG ATGGTGGTGCATGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCTG A G MDM4 Ensembl:ENSG00000198625 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1000461029 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_89387,RMVar_hsa_circ_92157,RMVar_hsa_circ_139148,RMVar_hsa_circ_139153,RMVar_hsa_circ_83671,RMVar_hsa_circ_139156,RMVar_hsa_circ_139157,RMVar_hsa_circ_119956,RMVar_hsa_circ_88043,RMVar_hsa_circ_91682,RMVar_hsa_circ_139158,RMVar_hsa_circ_139159 20224 RMVar_ID_20224 Human_SNP_ID_46830994 A-to-I Human chr1 + 204552344 204552344 204552344 AATGTCGTTGTTGGTTTTTTTTTTTTTTTTTGAGACAGTCTCACTCTGTTGCCCAGGCTGGAGTG AATGTCGTTGTTGGTTTTTTTTTTTTTTTTTGGGACAGTCTCACTCTGTTGCCCAGGCTGGAGTG A G MDM4 Ensembl:ENSG00000198625 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1248962543 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_89387,RMVar_hsa_circ_92157,RMVar_hsa_circ_139148,RMVar_hsa_circ_139153,RMVar_hsa_circ_83671,RMVar_hsa_circ_139156,RMVar_hsa_circ_139157,RMVar_hsa_circ_119956,RMVar_hsa_circ_88043,RMVar_hsa_circ_91682,RMVar_hsa_circ_139158,RMVar_hsa_circ_139159 20225 RMVar_ID_20225 Human_SNP_ID_46830995 A-to-I Human chr1 + 204552344 204552344 204552344 AATGTCGTTGTTGGTTTTTTTTTTTTTTTTTGAGACAGTCTCACTCTGTTGCCCAGGCTGGAGTG AATGTCGTTGTTGGTTTTTTTTTTTTTTTTTGTGACAGTCTCACTCTGTTGCCCAGGCTGGAGTG A T MDM4 Ensembl:ENSG00000198625 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1248962543 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_89387,RMVar_hsa_circ_92157,RMVar_hsa_circ_139148,RMVar_hsa_circ_139153,RMVar_hsa_circ_83671,RMVar_hsa_circ_139156,RMVar_hsa_circ_139157,RMVar_hsa_circ_119956,RMVar_hsa_circ_88043,RMVar_hsa_circ_91682,RMVar_hsa_circ_139158,RMVar_hsa_circ_139159 20226 RMVar_ID_20226 Human_SNP_ID_46831007 A-to-I Human chr1 + 204552384 204552384 204552384 TCACTCTGTTGCCCAGGCTGGAGTGCAATGGCATGATCTCTGCTCACCGCAACCTCTGCCTCCCG TCACTCTGTTGCCCAGGCTGGAGTGCAATGGCGTGATCTCTGCTCACCGCAACCTCTGCCTCCCG A G MDM4 Ensembl:ENSG00000198625 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1332789701 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10737130 RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_89387,RMVar_hsa_circ_92157,RMVar_hsa_circ_139148,RMVar_hsa_circ_139153,RMVar_hsa_circ_83671,RMVar_hsa_circ_139156,RMVar_hsa_circ_139157,RMVar_hsa_circ_119956,RMVar_hsa_circ_88043,RMVar_hsa_circ_91682,RMVar_hsa_circ_139158,RMVar_hsa_circ_139159 20227 RMVar_ID_20227 Human_SNP_ID_46831752 A-to-I Human chr1 + 204555174 204555174 204555174 GTAGAACTCTCCATTTCTTTTTTTTTTTTTTTAGACGGAGTCTCTCTCTGTCGCCCCGGCTGGAG GTAGAACTCTCCATTTCTTTTTTTTTTTTTTTGGACGGAGTCTCTCTCTGTCGCCCCGGCTGGAG A G MDM4 Ensembl:ENSG00000198625 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417944954 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5742629,Human_RBP_ID_8961511,Human_RBP_ID_10737333,Human_RBP_ID_23146138 RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_89387,RMVar_hsa_circ_92157,RMVar_hsa_circ_139148,RMVar_hsa_circ_139153,RMVar_hsa_circ_83671,RMVar_hsa_circ_139156,RMVar_hsa_circ_139157,RMVar_hsa_circ_119956,RMVar_hsa_circ_88043,RMVar_hsa_circ_91682,RMVar_hsa_circ_139158,RMVar_hsa_circ_139159 20228 RMVar_ID_20228 Human_SNP_ID_46831753 A-to-I Human chr1 + 204555174 204555174 204555174 GTAGAACTCTCCATTTCTTTTTTTTTTTTTTTAGACGGAGTCTCTCTCTGTCGCCCCGGCTGGAG GTAGAACTCTCCATTTCTTTTTTTTTTTTTTTTGACGGAGTCTCTCTCTGTCGCCCCGGCTGGAG A T MDM4 Ensembl:ENSG00000198625 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417944954 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5742629,Human_RBP_ID_8961511,Human_RBP_ID_10737333,Human_RBP_ID_23146138 RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_89387,RMVar_hsa_circ_92157,RMVar_hsa_circ_139148,RMVar_hsa_circ_139153,RMVar_hsa_circ_83671,RMVar_hsa_circ_139156,RMVar_hsa_circ_139157,RMVar_hsa_circ_119956,RMVar_hsa_circ_88043,RMVar_hsa_circ_91682,RMVar_hsa_circ_139158,RMVar_hsa_circ_139159 20229 RMVar_ID_20229 Human_SNP_ID_46831771 A-to-I Human chr1 + 204555210 204555210 204555210 GGAGTCTCTCTCTGTCGCCCCGGCTGGAGTGCAGTGGCGCGATCTCGGCTCACTGCAACCTCCGC GGAGTCTCTCTCTGTCGCCCCGGCTGGAGTGCGGTGGCGCGATCTCGGCTCACTGCAACCTCCGC A G MDM4 Ensembl:ENSG00000198625 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1300042596 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_618078,Human_miRNA_ID_866427 RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_89387,RMVar_hsa_circ_92157,RMVar_hsa_circ_139148,RMVar_hsa_circ_139153,RMVar_hsa_circ_83671,RMVar_hsa_circ_139156,RMVar_hsa_circ_139157,RMVar_hsa_circ_119956,RMVar_hsa_circ_88043,RMVar_hsa_circ_91682,RMVar_hsa_circ_139158,RMVar_hsa_circ_139159 20230 RMVar_ID_20230 Human_SNP_ID_46831776 A-to-I Human chr1 + 204555219 204555219 204555219 CTCTGTCGCCCCGGCTGGAGTGCAGTGGCGCGATCTCGGCTCACTGCAACCTCCGCCTCCCGGGT CTCTGTCGCCCCGGCTGGAGTGCAGTGGCGCGGTCTCGGCTCACTGCAACCTCCGCCTCCCGGGT A G MDM4 Ensembl:ENSG00000198625 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1429255876 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_866427 RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_89387,RMVar_hsa_circ_92157,RMVar_hsa_circ_139148,RMVar_hsa_circ_139153,RMVar_hsa_circ_83671,RMVar_hsa_circ_139156,RMVar_hsa_circ_139157,RMVar_hsa_circ_119956,RMVar_hsa_circ_88043,RMVar_hsa_circ_91682,RMVar_hsa_circ_139158,RMVar_hsa_circ_139159 20231 RMVar_ID_20231 Human_SNP_ID_46831785 A-to-I Human chr1 + 204555234 204555234 204555234 TGGAGTGCAGTGGCGCGATCTCGGCTCACTGCAACCTCCGCCTCCCGGGTTCACCCCATTCTCCT TGGAGTGCAGTGGCGCGATCTCGGCTCACTGCGACCTCCGCCTCCCGGGTTCACCCCATTCTCCT A G MDM4 Ensembl:ENSG00000198625 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1028887182 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_89387,RMVar_hsa_circ_92157,RMVar_hsa_circ_139148,RMVar_hsa_circ_139153,RMVar_hsa_circ_83671,RMVar_hsa_circ_139156,RMVar_hsa_circ_139157,RMVar_hsa_circ_119956,RMVar_hsa_circ_88043,RMVar_hsa_circ_91682,RMVar_hsa_circ_139158,RMVar_hsa_circ_139159 20232 RMVar_ID_20232 Human_SNP_ID_46831800 A-to-I Human chr1 + 204555281 204555281 204555281 GGTTCACCCCATTCTCCTGCCTCAGCCTCCCTAGTAGCTGGGACTATAGGCGCCCGCCACCACGC GGTTCACCCCATTCTCCTGCCTCAGCCTCCCTGGTAGCTGGGACTATAGGCGCCCGCCACCACGC A G MDM4 Ensembl:ENSG00000198625 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs529558917 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_89387,RMVar_hsa_circ_92157,RMVar_hsa_circ_139148,RMVar_hsa_circ_139153,RMVar_hsa_circ_83671,RMVar_hsa_circ_139156,RMVar_hsa_circ_139157,RMVar_hsa_circ_119956,RMVar_hsa_circ_88043,RMVar_hsa_circ_91682,RMVar_hsa_circ_139158,RMVar_hsa_circ_139159 20233 RMVar_ID_20233 Human_SNP_ID_46831804 A-to-I Human chr1 + 204555294 204555294 204555294 CTCCTGCCTCAGCCTCCCTAGTAGCTGGGACTATAGGCGCCCGCCACCACGCCTGGCTAATTTTT CTCCTGCCTCAGCCTCCCTAGTAGCTGGGACTGTAGGCGCCCGCCACCACGCCTGGCTAATTTTT A G MDM4 Ensembl:ENSG00000198625 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1411357843 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_89387,RMVar_hsa_circ_92157,RMVar_hsa_circ_139148,RMVar_hsa_circ_139153,RMVar_hsa_circ_83671,RMVar_hsa_circ_139156,RMVar_hsa_circ_139157,RMVar_hsa_circ_119956,RMVar_hsa_circ_88043,RMVar_hsa_circ_91682,RMVar_hsa_circ_139158,RMVar_hsa_circ_139159 20234 RMVar_ID_20234 Human_SNP_ID_46831815 A-to-I Human chr1 + 204555329 204555329 204555329 GGCGCCCGCCACCACGCCTGGCTAATTTTTGTATTTTTATTGGAGACGGGGTTTCACCGTCTTAG GGCGCCCGCCACCACGCCTGGCTAATTTTTGTGTTTTTATTGGAGACGGGGTTTCACCGTCTTAG A G MDM4 Ensembl:ENSG00000198625 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs551497021 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10737336 RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_89387,RMVar_hsa_circ_92157,RMVar_hsa_circ_139148,RMVar_hsa_circ_139153,RMVar_hsa_circ_83671,RMVar_hsa_circ_139156,RMVar_hsa_circ_139157,RMVar_hsa_circ_119956,RMVar_hsa_circ_88043,RMVar_hsa_circ_91682,RMVar_hsa_circ_139158,RMVar_hsa_circ_139159 20235 RMVar_ID_20235 Human_SNP_ID_46831817 A-to-I Human chr1 + 204555335 204555335 204555335 CGCCACCACGCCTGGCTAATTTTTGTATTTTTATTGGAGACGGGGTTTCACCGTCTTAGCCAGGA CGCCACCACGCCTGGCTAATTTTTGTATTTTTTTTGGAGACGGGGTTTCACCGTCTTAGCCAGGA A T MDM4 Ensembl:ENSG00000198625 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs950305384 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10737338 RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_89387,RMVar_hsa_circ_92157,RMVar_hsa_circ_139148,RMVar_hsa_circ_139153,RMVar_hsa_circ_83671,RMVar_hsa_circ_139156,RMVar_hsa_circ_139157,RMVar_hsa_circ_119956,RMVar_hsa_circ_88043,RMVar_hsa_circ_91682,RMVar_hsa_circ_139158,RMVar_hsa_circ_139159 20236 RMVar_ID_20236 Human_SNP_ID_46831825 A-to-I Human chr1 + 204555364 204555364 204555364 TTTATTGGAGACGGGGTTTCACCGTCTTAGCCAGGATGGTCTTGATCTCCTGACCTCGTGATCTG TTTATTGGAGACGGGGTTTCACCGTCTTAGCCGGGATGGTCTTGATCTCCTGACCTCGTGATCTG A G MDM4 Ensembl:ENSG00000198625 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1301011559 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_89387,RMVar_hsa_circ_92157,RMVar_hsa_circ_139148,RMVar_hsa_circ_139153,RMVar_hsa_circ_83671,RMVar_hsa_circ_139156,RMVar_hsa_circ_139157,RMVar_hsa_circ_119956,RMVar_hsa_circ_88043,RMVar_hsa_circ_91682,RMVar_hsa_circ_139158,RMVar_hsa_circ_139159 20237 RMVar_ID_20237 Human_SNP_ID_46831927 A-to-I Human chr1 + 204555761 204555761 204555761 GTGGCGTGCACCTGTAGTCCCAGCTACTTGGCAGGTTGAGACAGGAGAATCGCTTGAACCTGGGA GTGGCGTGCACCTGTAGTCCCAGCTACTTGGCGGGTTGAGACAGGAGAATCGCTTGAACCTGGGA A G MDM4 Ensembl:ENSG00000198625 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs372649108 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5742636,Human_RBP_ID_10737348 RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_89387,RMVar_hsa_circ_92157,RMVar_hsa_circ_139148,RMVar_hsa_circ_139153,RMVar_hsa_circ_83671,RMVar_hsa_circ_139156,RMVar_hsa_circ_139157,RMVar_hsa_circ_119956,RMVar_hsa_circ_88043,RMVar_hsa_circ_91682,RMVar_hsa_circ_139158,RMVar_hsa_circ_139159 20238 RMVar_ID_20238 Human_SNP_ID_46831934 A-to-I Human chr1 + 204555806 204555806 204555806 AGAATCGCTTGAACCTGGGAGGTGGAGGTTGCAGTGAGCCGAGACTGCACCACTGCGCTCCCACC AGAATCGCTTGAACCTGGGAGGTGGAGGTTGCGGTGAGCCGAGACTGCACCACTGCGCTCCCACC A G MDM4 Ensembl:ENSG00000198625 Protein coding 3'UTR GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1187235865 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_89387,RMVar_hsa_circ_92157,RMVar_hsa_circ_139148,RMVar_hsa_circ_139153,RMVar_hsa_circ_83671,RMVar_hsa_circ_139156,RMVar_hsa_circ_139157,RMVar_hsa_circ_119956,RMVar_hsa_circ_88043,RMVar_hsa_circ_91682,RMVar_hsa_circ_139158,RMVar_hsa_circ_139159 20239 RMVar_ID_20239 Human_SNP_ID_46831939 A-to-I Human chr1 + 204555822 204555822 204555822 GGGAGGTGGAGGTTGCAGTGAGCCGAGACTGCACCACTGCGCTCCCACCTGGGTGACAGAGACTC GGGAGGTGGAGGTTGCAGTGAGCCGAGACTGCGCCACTGCGCTCCCACCTGGGTGACAGAGACTC A G MDM4 Ensembl:ENSG00000198625 Protein coding 3'UTR GSE100210;GSE99789;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BERP35T1 cell line - 29129909,29796672,31158229 RNA-Seq:(High) rs1482443128 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223152,Human_RBP_ID_5742638,Human_RBP_ID_10737349,Human_RBP_ID_23146143 RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_89387,RMVar_hsa_circ_92157,RMVar_hsa_circ_139148,RMVar_hsa_circ_139153,RMVar_hsa_circ_83671,RMVar_hsa_circ_139156,RMVar_hsa_circ_139157,RMVar_hsa_circ_119956,RMVar_hsa_circ_88043,RMVar_hsa_circ_91682,RMVar_hsa_circ_139158,RMVar_hsa_circ_139159 20240 RMVar_ID_20240 Human_SNP_ID_46831941 A-to-I Human chr1 + 204555825 204555825 204555825 AGGTGGAGGTTGCAGTGAGCCGAGACTGCACCACTGCGCTCCCACCTGGGTGACAGAGACTCTGT AGGTGGAGGTTGCAGTGAGCCGAGACTGCACCTCTGCGCTCCCACCTGGGTGACAGAGACTCTGT A T MDM4 Ensembl:ENSG00000198625 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1487204554 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223152,Human_RBP_ID_5742638,Human_RBP_ID_10737349,Human_RBP_ID_23146143 RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_89387,RMVar_hsa_circ_92157,RMVar_hsa_circ_139148,RMVar_hsa_circ_139153,RMVar_hsa_circ_83671,RMVar_hsa_circ_139156,RMVar_hsa_circ_139157,RMVar_hsa_circ_119956,RMVar_hsa_circ_88043,RMVar_hsa_circ_91682,RMVar_hsa_circ_139158,RMVar_hsa_circ_139159 20241 RMVar_ID_20241 Human_SNP_ID_46832113 A-to-I Human chr1 + 204556443 204556443 204556443 GGTCAGGCCAGGCGCGGTGGTTCACTCCTGTTATTCCAGCACTGGGGTGGCCAAAGTGGGCAGAT GGTCAGGCCAGGCGCGGTGGTTCACTCCTGTTGTTCCAGCACTGGGGTGGCCAAAGTGGGCAGAT A G MDM4 Ensembl:ENSG00000198625 Protein coding 3'UTR GSE100210;GSE107867 HepG2 cell line;ASD brains,frontal_cortex - 29129909,30559470 RNA-Seq:(High) rs1558346964 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4018835,Human_RBP_ID_17763071 Human_miRNA_ID_2673973,Human_miRNA_ID_2773232,Human_miRNA_ID_2924729 RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_89387,RMVar_hsa_circ_92157,RMVar_hsa_circ_139148,RMVar_hsa_circ_139153,RMVar_hsa_circ_83671,RMVar_hsa_circ_139156,RMVar_hsa_circ_139157,RMVar_hsa_circ_119956,RMVar_hsa_circ_88043,RMVar_hsa_circ_91682,RMVar_hsa_circ_139158,RMVar_hsa_circ_139159 20242 RMVar_ID_20242 Human_SNP_ID_46832114 A-to-I Human chr1 + 204556448 204556448 204556448 GGCCAGGCGCGGTGGTTCACTCCTGTTATTCCAGCACTGGGGTGGCCAAAGTGGGCAGATTGCTT GGCCAGGCGCGGTGGTTCACTCCTGTTATTCCGGCACTGGGGTGGCCAAAGTGGGCAGATTGCTT A G MDM4 Ensembl:ENSG00000198625 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs116236468 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17763071 Human_miRNA_ID_1510304,Human_miRNA_ID_1640606,Human_miRNA_ID_2673973,Human_miRNA_ID_2773232,Human_miRNA_ID_2924729 RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_89387,RMVar_hsa_circ_92157,RMVar_hsa_circ_139148,RMVar_hsa_circ_139153,RMVar_hsa_circ_83671,RMVar_hsa_circ_139156,RMVar_hsa_circ_139157,RMVar_hsa_circ_119956,RMVar_hsa_circ_88043,RMVar_hsa_circ_91682,RMVar_hsa_circ_139158,RMVar_hsa_circ_139159 20243 RMVar_ID_20243 Human_SNP_ID_46832128 A-to-I Human chr1 + 204556501 204556501 204556501 GGCAGATTGCTTGCGCTCTGGAGCTCGAGACCAGCCTGGGCAACATGGTGAAACCCTGTCTCTAC GGCAGATTGCTTGCGCTCTGGAGCTCGAGACCGGCCTGGGCAACATGGTGAAACCCTGTCTCTAC A G MDM4 Ensembl:ENSG00000198625 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs755388016 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10737391 RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_89387,RMVar_hsa_circ_92157,RMVar_hsa_circ_139148,RMVar_hsa_circ_139153,RMVar_hsa_circ_83671,RMVar_hsa_circ_139156,RMVar_hsa_circ_139157,RMVar_hsa_circ_119956,RMVar_hsa_circ_88043,RMVar_hsa_circ_91682,RMVar_hsa_circ_139158,RMVar_hsa_circ_139159 20244 RMVar_ID_20244 Human_SNP_ID_46832129 A-to-I Human chr1 + 204556513 204556513 204556513 GCGCTCTGGAGCTCGAGACCAGCCTGGGCAACATGGTGAAACCCTGTCTCTACCAAAAATACAAA GCGCTCTGGAGCTCGAGACCAGCCTGGGCAACCTGGTGAAACCCTGTCTCTACCAAAAATACAAA A C MDM4 Ensembl:ENSG00000198625 Protein coding 3'UTR GSE38233;GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,32596459 RNA-Seq:(High) rs779502088 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_99138 RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_89387,RMVar_hsa_circ_92157,RMVar_hsa_circ_139148,RMVar_hsa_circ_139153,RMVar_hsa_circ_83671,RMVar_hsa_circ_139156,RMVar_hsa_circ_139157,RMVar_hsa_circ_119956,RMVar_hsa_circ_88043,RMVar_hsa_circ_91682,RMVar_hsa_circ_139158,RMVar_hsa_circ_139159 20245 RMVar_ID_20245 Human_SNP_ID_46832132 A-to-I Human chr1 + 204556520 204556520 204556520 GGAGCTCGAGACCAGCCTGGGCAACATGGTGAAACCCTGTCTCTACCAAAAATACAAAAAAAAAG GGAGCTCGAGACCAGCCTGGGCAACATGGTGAGACCCTGTCTCTACCAAAAATACAAAAAAAAAG A G MDM4 Ensembl:ENSG00000198625 Protein coding 3'UTR GSE47997;GSE100210;GSE99789 K562 cells&HepG2 cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 23474544,29129909,29796672 RNA-Seq:(High) rs1247732440 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_99138 RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_89387,RMVar_hsa_circ_92157,RMVar_hsa_circ_139148,RMVar_hsa_circ_139153,RMVar_hsa_circ_83671,RMVar_hsa_circ_139156,RMVar_hsa_circ_139157,RMVar_hsa_circ_119956,RMVar_hsa_circ_88043,RMVar_hsa_circ_91682,RMVar_hsa_circ_139158,RMVar_hsa_circ_139159 20246 RMVar_ID_20246 Human_SNP_ID_46832135 A-to-I Human chr1 + 204556536 204556536 204556536 CTGGGCAACATGGTGAAACCCTGTCTCTACCAAAAATACAAAAAAAAAGCTGGGCATGGTGGGTG CTGGGCAACATGGTGAAACCCTGTCTCTACCACAAATACAAAAAAAAAGCTGGGCATGGTGGGTG A C MDM4 Ensembl:ENSG00000198625 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1254739586 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10737395,Human_RBP_ID_17736074 RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_89387,RMVar_hsa_circ_92157,RMVar_hsa_circ_139148,RMVar_hsa_circ_139153,RMVar_hsa_circ_83671,RMVar_hsa_circ_139156,RMVar_hsa_circ_139157,RMVar_hsa_circ_119956,RMVar_hsa_circ_88043,RMVar_hsa_circ_91682,RMVar_hsa_circ_139158,RMVar_hsa_circ_139159 20247 RMVar_ID_20247 Human_SNP_ID_46832137 A-to-I Human chr1 + 204556544 204556542 204556545 CATGGTGAAACCCTGTCTCTACCAAAAATACAAAAAAAAAGCTGGGCATGGTGGGTGCATGCTTG CATGGTGAAACCCTGTCTCTACCAAAAATAC___AAAAAAGCTGGGCATGGTGGGTGCATGCTTG CAAA C MDM4 Ensembl:ENSG00000198625 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs912727628 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_10737395,Human_RBP_ID_17736074,Human_RBP_ID_24625344 RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_89387,RMVar_hsa_circ_92157,RMVar_hsa_circ_139148,RMVar_hsa_circ_139153,RMVar_hsa_circ_83671,RMVar_hsa_circ_139156,RMVar_hsa_circ_139157,RMVar_hsa_circ_119956,RMVar_hsa_circ_88043,RMVar_hsa_circ_91682,RMVar_hsa_circ_139158,RMVar_hsa_circ_139159 20248 RMVar_ID_20248 Human_SNP_ID_46832152 A-to-I Human chr1 + 204556581 204556581 204556581 AAAGCTGGGCATGGTGGGTGCATGCTTGTCCCAGCTACTGAGGAGGCTGAGGTGGGAGGATCGCT AAAGCTGGGCATGGTGGGTGCATGCTTGTCCCGGCTACTGAGGAGGCTGAGGTGGGAGGATCGCT A G MDM4 Ensembl:ENSG00000198625 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1175773316 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_272235 RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_89387,RMVar_hsa_circ_92157,RMVar_hsa_circ_139148,RMVar_hsa_circ_139153,RMVar_hsa_circ_83671,RMVar_hsa_circ_139156,RMVar_hsa_circ_139157,RMVar_hsa_circ_119956,RMVar_hsa_circ_88043,RMVar_hsa_circ_91682,RMVar_hsa_circ_139158,RMVar_hsa_circ_139159 20249 RMVar_ID_20249 Human_SNP_ID_46832155 A-to-I Human chr1 + 204556598 204556598 204556598 GTGCATGCTTGTCCCAGCTACTGAGGAGGCTGAGGTGGGAGGATCGCTTGAGCCTGGGAGGTGGA GTGCATGCTTGTCCCAGCTACTGAGGAGGCTGGGGTGGGAGGATCGCTTGAGCCTGGGAGGTGGA A G MDM4 Ensembl:ENSG00000198625 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs11556785 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_89387,RMVar_hsa_circ_92157,RMVar_hsa_circ_139148,RMVar_hsa_circ_139153,RMVar_hsa_circ_83671,RMVar_hsa_circ_139156,RMVar_hsa_circ_139157,RMVar_hsa_circ_119956,RMVar_hsa_circ_88043,RMVar_hsa_circ_91682,RMVar_hsa_circ_139158,RMVar_hsa_circ_139159 20250 RMVar_ID_20250 Human_SNP_ID_46832157 A-to-I Human chr1 + 204556616 204556616 204556616 TACTGAGGAGGCTGAGGTGGGAGGATCGCTTGAGCCTGGGAGGTGGAGGTTGCAGTGAGCTGAGA TACTGAGGAGGCTGAGGTGGGAGGATCGCTTGGGCCTGGGAGGTGGAGGTTGCAGTGAGCTGAGA A G MDM4 Ensembl:ENSG00000198625 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,31158229,31158229,32596459 RNA-Seq:(High) rs924510125 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_89387,RMVar_hsa_circ_92157,RMVar_hsa_circ_139148,RMVar_hsa_circ_139153,RMVar_hsa_circ_83671,RMVar_hsa_circ_139156,RMVar_hsa_circ_139157,RMVar_hsa_circ_119956,RMVar_hsa_circ_88043,RMVar_hsa_circ_91682,RMVar_hsa_circ_139158,RMVar_hsa_circ_139159 20251 RMVar_ID_20251 Human_SNP_ID_46832419 A-to-I Human chr1 + 204557582 204557582 204557582 GCACCACCACACCTGGCTAATTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGC GCACCACCACACCTGGCTAATTTTGTATTTTTGGTAGAGACAGGGTTTCACCATGTTGGCCAGGC A G MDM4 Ensembl:ENSG00000198625 Protein coding 3'UTR GSE38233;GSE99789;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29796672,31158229 RNA-Seq:(High) rs1463804308 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_99139 RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_89387,RMVar_hsa_circ_92157,RMVar_hsa_circ_139148,RMVar_hsa_circ_139153,RMVar_hsa_circ_83671,RMVar_hsa_circ_139156,RMVar_hsa_circ_139157,RMVar_hsa_circ_119956,RMVar_hsa_circ_88043,RMVar_hsa_circ_91682,RMVar_hsa_circ_139158,RMVar_hsa_circ_139159 20252 RMVar_ID_20252 Human_SNP_ID_46832428 A-to-I Human chr1 + 204557599 204557599 204557599 TAATTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGA TAATTTTGTATTTTTAGTAGAGACAGGGTTTCGCCATGTTGGCCAGGCTGGTCTTGAACTCCTGA A G MDM4 Ensembl:ENSG00000198625 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1353915520 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_89387,RMVar_hsa_circ_92157,RMVar_hsa_circ_139148,RMVar_hsa_circ_139153,RMVar_hsa_circ_83671,RMVar_hsa_circ_139156,RMVar_hsa_circ_139157,RMVar_hsa_circ_119956,RMVar_hsa_circ_88043,RMVar_hsa_circ_91682,RMVar_hsa_circ_139158,RMVar_hsa_circ_139159 20253 RMVar_ID_20253 Human_SNP_ID_46832446 A-to-I Human chr1 + 204557667 204557667 204557667 CAGGCGATCTGCCCGCCTTGGCCTCCCAAAGTACTGGGATTACAGGCGTGAGCAACTGCTCCTGG CAGGCGATCTGCCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCAACTGCTCCTGG A G MDM4 Ensembl:ENSG00000198625 Protein coding 3'UTR GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490829,GSM3490830,GSM3490831 esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,EC109 cell line - 29796672,31158229,31158229,32596459 RNA-Seq:(High) rs1364026479 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_156318,Human_miRNA_ID_1350863,Human_miRNA_ID_2678205,Human_miRNA_ID_3080254 RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_89387,RMVar_hsa_circ_92157,RMVar_hsa_circ_139148,RMVar_hsa_circ_139153,RMVar_hsa_circ_83671,RMVar_hsa_circ_139156,RMVar_hsa_circ_139157,RMVar_hsa_circ_119956,RMVar_hsa_circ_88043,RMVar_hsa_circ_91682,RMVar_hsa_circ_139158,RMVar_hsa_circ_139159 20254 RMVar_ID_20254 Human_SNP_ID_46840466 A-to-I Human chr1 - 204590284 204590284 204590284 ACTTTTCAAGTTGGGCACAGTGTCTCAGGCCTATAATCCCAGCACTTTGGGAGGCCAAGGCAGGT ACTTTTCAAGTTGGGCACAGTGTCTCAGGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924546108 Functional Loss SNV dbSNP153 33..33 33 - - - 20255 RMVar_ID_20255 Human_SNP_ID_46854242 A-to-I Human chr1 - 204649344 204649344 204649344 CCAGGCCGTGAGCTGCGGATACAGAGATAAATAAGACCTATCCCTGCCCTCTAGGACCTCACAGT CCAGGCCGTGAGCTGCGGATACAGAGATAAATGAGACCTATCCCTGCCCTCTAGGACCTCACAGT T C LRRN2 Ensembl:ENSG00000170382 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs546260539 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139171 20256 RMVar_ID_20256 Human_SNP_ID_46858954 A-to-I Human chr1 - 204670060 204670060 204670060 GCTGTATCCACTCTTGCATCTCCAATTGTCAGAGAAGCCAAGGGAAAAGAAAGTGTCAGAAAAAA GCTGTATCCACTCTTGCATCTCCAATTGTCAGCGAAGCCAAGGGAAAAGAAAGTGTCAGAAAAAA T G LRRN2 Ensembl:ENSG00000170382 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1390398502 Functional Loss SNV dbSNP153 33..33 33 - - - 20257 RMVar_ID_20257 Human_SNP_ID_46962927 A-to-I Human chr1 - 205102831 205102831 205102831 TCATCACCACACCTGGCTAATTTTGTATTTTTAGTAGAGACGGGGTCTCTCCATGTTGATCAGGC TCATCACCACACCTGGCTAATTTTGTATTTTTTGTAGAGACGGGGTCTCTCCATGTTGATCAGGC T A RBBP5 Ensembl:ENSG00000117222 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1351997122 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139178,RMVar_hsa_circ_329122,RMVar_hsa_circ_355172,RMVar_hsa_circ_29541,RMVar_hsa_circ_63655 20258 RMVar_ID_20258 Human_SNP_ID_46962959 A-to-I Human chr1 - 205102949 205102949 205102949 TCTTGTTGTTGCCCAGGCTGGAGTGCAATGGCACCATCTCAGTTCACCGCAACCTCTCCCTCCCG TCTTGTTGTTGCCCAGGCTGGAGTGCAATGGCGCCATCTCAGTTCACCGCAACCTCTCCCTCCCG T C RBBP5 Ensembl:ENSG00000117222 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs989793940 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139178,RMVar_hsa_circ_329122,RMVar_hsa_circ_355172,RMVar_hsa_circ_29541,RMVar_hsa_circ_63655 20259 RMVar_ID_20259 Human_SNP_ID_46966509 A-to-I Human chr1 - 205117211 205117211 205117211 TGTCTCTACTAAAAATACAAAATTAGCCGGGCATGGTGCCACATGCCTGTAATCCCAGCTGCTGC TGTCTCTACTAAAAATACAAAATTAGCCGGGCGTGGTGCCACATGCCTGTAATCCCAGCTGCTGC T C RBBP5 Ensembl:ENSG00000117222 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1219523969 Functional Loss SNV dbSNP153 33..33 33 - - - 20260 RMVar_ID_20260 Human_SNP_ID_46966604 A-to-I Human chr1 - 205117621 205117621 205117621 AGTTTCCCTCTTGTTGCCCAGGCTGGAGTGCAATGGTGTGACCTCGGCTCACTGCAACCTCTGCC AGTTTCCCTCTTGTTGCCCAGGCTGGAGTGCAGTGGTGTGACCTCGGCTCACTGCAACCTCTGCC T C RBBP5 Ensembl:ENSG00000117222 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1442145315 Functional Loss SNV dbSNP153 33..33 33 - - - 20261 RMVar_ID_20261 Human_SNP_ID_46967004 A-to-I Human chr1 - 205119227 205119227 205119227 CCACACCTGGCTATATTTTTTGTATTTTTAGTAGAGACTGGGTTTCACCATGTTGGCCAACCTGG CCACACCTGGCTATATTTTTTGTATTTTTAGTGGAGACTGGGTTTCACCATGTTGGCCAACCTGG T C RBBP5 Ensembl:ENSG00000117222 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1351919563 Functional Loss SNV dbSNP153 33..33 33 - - - 20262 RMVar_ID_20262 Human_SNP_ID_46967005 A-to-I Human chr1 - 205119230 205119230 205119230 ACACCACACCTGGCTATATTTTTTGTATTTTTAGTAGAGACTGGGTTTCACCATGTTGGCCAACC ACACCACACCTGGCTATATTTTTTGTATTTTTGGTAGAGACTGGGTTTCACCATGTTGGCCAACC T C RBBP5 Ensembl:ENSG00000117222 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs920753164 Functional Loss SNV dbSNP153 33..33 33 - - - 20263 RMVar_ID_20263 Human_SNP_ID_46980620 A-to-I Human chr1 - 205177085 205177085 205177085 TTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTATAGGTGGGTGTCACCATACCCGGCTAATTTGT TTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTGTAGGTGGGTGTCACCATACCCGGCTAATTTGT T C DSTYK Ensembl:ENSG00000133059 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs777851150 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_371074,RMVar_hsa_circ_139188,RMVar_hsa_circ_65658,RMVar_hsa_circ_373486,RMVar_hsa_circ_139194,RMVar_hsa_circ_345146,RMVar_hsa_circ_139199,RMVar_hsa_circ_370705,RMVar_hsa_circ_139203,RMVar_hsa_circ_139201,RMVar_hsa_circ_114653,RMVar_hsa_circ_315537,RMVar_hsa_circ_139202 20264 RMVar_ID_20264 Human_SNP_ID_46980644 A-to-I Human chr1 - 205177204 205177204 205177204 CTTTTTGTTTGTATGTTTGTTTATATTTTAGAAATAGGGTCTCACTCTGTTGTTCAGGCTAGAGT CTTTTTGTTTGTATGTTTGTTTATATTTTAGAGATAGGGTCTCACTCTGTTGTTCAGGCTAGAGT T C DSTYK Ensembl:ENSG00000133059 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1186913422 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10739335 RMVar_hsa_circ_371074,RMVar_hsa_circ_139188,RMVar_hsa_circ_65658,RMVar_hsa_circ_373486,RMVar_hsa_circ_139194,RMVar_hsa_circ_345146,RMVar_hsa_circ_139199,RMVar_hsa_circ_370705,RMVar_hsa_circ_139203,RMVar_hsa_circ_139201,RMVar_hsa_circ_114653,RMVar_hsa_circ_315537,RMVar_hsa_circ_139202 20265 RMVar_ID_20265 Human_SNP_ID_46984273 A-to-I Human chr1 - 205192823 205192823 205192823 AGTTTCGCTCTTGTCACTCAGACTGGAGTGCAATGGCGTTATCTCGGCTCACTACAACCTCTGCC AGTTTCGCTCTTGTCACTCAGACTGGAGTGCAGTGGCGTTATCTCGGCTCACTACAACCTCTGCC T C DSTYK Ensembl:ENSG00000133059 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs908151133 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114653,RMVar_hsa_circ_139202 20266 RMVar_ID_20266 Human_SNP_ID_46986805 A-to-I Human chr1 - 205203387 205203387 205203387 ACCTCTGCCTCCTAGATAAAAATGATTCTCCTACCTCAGCCTCCCAAGTAGCTGGGACTGCAGGC ACCTCTGCCTCCTAGATAAAAATGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTGCAGGC T C DSTYK Ensembl:ENSG00000133059 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1558627822 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114653,RMVar_hsa_circ_139202 20267 RMVar_ID_20267 Human_SNP_ID_46988151 A-to-I Human chr1 - 205208671 205208671 205208671 TGGGGTCTCACTTTGTTGCCCAGGCTGGTCTCAAACTCATGGCCTCAAACGATCCTTCCAACTCA TGGGGTCTCACTTTGTTGCCCAGGCTGGTCTCGAACTCATGGCCTCAAACGATCCTTCCAACTCA T C DSTYK Ensembl:ENSG00000133059 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1452135159 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114653,RMVar_hsa_circ_139202 20268 RMVar_ID_20268 Human_SNP_ID_47070716 A-to-I Human chr1 + 205545261 205545261 205545261 GAACTCCTGACCTCAGGTGATCCCGCTGCCTCAGCTTCCAAAGTGCTAAGATTACAGGCGTGAGC GAACTCCTGACCTCAGGTGATCCCGCTGCCTCGGCTTCCAAAGTGCTAAGATTACAGGCGTGAGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167492452 Functional Loss SNV dbSNP153 33..33 33 - - - 20269 RMVar_ID_20269 Human_SNP_ID_47089095 A-to-I Human chr1 - 205618118 205618118 205618118 GGGAGGCTGAGGTGGGAGGACCGCTTGAGCCCAGTAGATCAAGGCTGCAGTGAGCTATAATGGCA GGGAGGCTGAGGTGGGAGGACCGCTTGAGCCCGGTAGATCAAGGCTGCAGTGAGCTATAATGGCA T C ELK4 Ensembl:ENSG00000158711 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs928582781 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2552465,Human_miRNA_ID_2552466 RMVar_hsa_circ_139219,RMVar_hsa_circ_67610,RMVar_hsa_circ_313856,RMVar_hsa_circ_325050,RMVar_hsa_circ_139216,RMVar_hsa_circ_124268,RMVar_hsa_circ_355004,RMVar_hsa_circ_273287,RMVar_hsa_circ_139221,RMVar_hsa_circ_98239,RMVar_hsa_circ_139220 20270 RMVar_ID_20270 Human_SNP_ID_47090335 A-to-I Human chr1 - 205622492 205622492 205622492 GTGCCCAGGAGGCTGAGGCAGGAGGATCACTTAAGCTCAAGTGGTTGAGGCTGCAGTGAGCCATG GTGCCCAGGAGGCTGAGGCAGGAGGATCACTTGAGCTCAAGTGGTTGAGGCTGCAGTGAGCCATG T C ELK4 Ensembl:ENSG00000158711 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1415906500 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24625738 RMVar_hsa_circ_139219,RMVar_hsa_circ_313856,RMVar_hsa_circ_139216,RMVar_hsa_circ_124268,RMVar_hsa_circ_273287,RMVar_hsa_circ_139221,RMVar_hsa_circ_98239,RMVar_hsa_circ_139220,RMVar_hsa_circ_139223,RMVar_hsa_circ_333884 20271 RMVar_ID_20271 Human_SNP_ID_47115485 A-to-I Human chr1 - 205724473 205724473 205724473 GCCAGGCTGGTCTTGAACTCCTGGCCTCCAGCAATCTGCCTACCTCAGCCACCCAAACTGCTGAG GCCAGGCTGGTCTTGAACTCCTGGCCTCCAGCGATCTGCCTACCTCAGCCACCCAAACTGCTGAG T C NUCKS1 Ensembl:ENSG00000069275 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs823108 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100041,RMVar_hsa_circ_373543,RMVar_hsa_circ_347275,RMVar_hsa_circ_139227,RMVar_hsa_circ_139229,RMVar_hsa_circ_139230,RMVar_hsa_circ_290953,RMVar_hsa_circ_364321 20272 RMVar_ID_20272 Human_SNP_ID_47116608 A-to-I Human chr1 - 205729850 205729850 205729850 CGCTTGGCTAATTTTGTGTTTTTAGTAGAGACAAGGTTTCTCTATGTTGGTTAGGCTGATCTCAA CGCTTGGCTAATTTTGTGTTTTTAGTAGAGACGAGGTTTCTCTATGTTGGTTAGGCTGATCTCAA T C NUCKS1 Ensembl:ENSG00000069275 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1320018669 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10741307 20273 RMVar_ID_20273 Human_SNP_ID_47116630 A-to-I Human chr1 - 205729938 205729938 205729938 CGGCTCACCACAACCTCTGACCCCTGGGTTCAAGTGATTCTCCTACCTCAGCTTCCCAAGTAGCA CGGCTCACCACAACCTCTGACCCCTGGGTTCAGGTGATTCTCCTACCTCAGCTTCCCAAGTAGCA T C NUCKS1 Ensembl:ENSG00000069275 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs182934830 Functional Loss SNV dbSNP153 33..33 33 - - - 20274 RMVar_ID_20274 Human_SNP_ID_47117446 A-to-I Human chr1 - 205732961 205732958 205732961 AATGGTCGTGTTTGCATTATGATCATCATACTATTTTTCATGGCATTTGTCATTAAAAAATCACT AATGGTCGTGTTTGCATTATGATCATCATACT___TTTCATGGCATTTGTCATTAAAAAATCACT AAAT A NUCKS1 Ensembl:ENSG00000069275 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1450327030 Functional Loss DEL dbSNP153 33..35 33 - - - 20275 RMVar_ID_20275 Human_SNP_ID_47117448 A-to-I Human chr1 - 205732961 205732961 205732961 AATGGTCGTGTTTGCATTATGATCATCATACTATTTTTCATGGCATTTGTCATTAAAAAATCACT AATGGTCGTGTTTGCATTATGATCATCATACTGTTTTTCATGGCATTTGTCATTAAAAAATCACT T C NUCKS1 Ensembl:ENSG00000069275 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1473416602 Functional Loss SNV dbSNP153 33..33 33 - - - 20276 RMVar_ID_20276 Human_SNP_ID_47117451 A-to-I Human chr1 - 205732975 205732975 205732975 TAAATAATACAGAAAATGGTCGTGTTTGCATTATGATCATCATACTATTTTTCATGGCATTTGTC TAAATAATACAGAAAATGGTCGTGTTTGCATTGTGATCATCATACTATTTTTCATGGCATTTGTC T C NUCKS1 Ensembl:ENSG00000069275 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs377391114 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5744286,Human_RBP_ID_22853043 20277 RMVar_ID_20277 Human_SNP_ID_47117621 A-to-I Human chr1 - 205733733 205733733 205733733 AATTTTTAATGACAAATGCCATGAAAAACAGTATTGTGATCATAATGCAATATGATCATTTGCAG AATTTTTAATGACAAATGCCATGAAAAACAGTGTTGTGATCATAATGCAATATGATCATTTGCAG T C NUCKS1 Ensembl:ENSG00000069275 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs975179513 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8295993 20278 RMVar_ID_20278 Human_SNP_ID_47117701 A-to-I Human chr1 - 205734078 205734077 205734079 GGCCAGGAGTTTGAGACCAGCATGGGAAACATAGAAAGGCCCCGTCTCTACAAAAAAAAAAAATT GGCCAGGAGTTTGAGACCAGCATGGGAAACA__GAAAGGCCCCGTCTCTACAAAAAAAAAAAATT CTA C NUCKS1 Ensembl:ENSG00000069275 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1223989773 Functional Loss DEL dbSNP153 32..33 33 - - - 20279 RMVar_ID_20279 Human_SNP_ID_47117720 A-to-I Human chr1 - 205734158 205734158 205734158 TAACAAGTTACAGGCCAGGCCTGGTGGCTCACACCTGTAATCCCAGCATTTTGGGAGATTAAGGT TAACAAGTTACAGGCCAGGCCTGGTGGCTCACGCCTGTAATCCCAGCATTTTGGGAGATTAAGGT T C NUCKS1 Ensembl:ENSG00000069275 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1028073557 Functional Loss SNV dbSNP153 33..33 33 - - - 20280 RMVar_ID_20280 Human_SNP_ID_47117879 A-to-I Human chr1 - 205734876 205734876 205734876 TTTATTTTTTTTTTGAGATGGAGTCTTGCTCTATCACCCAGGCTGGAGTGCAGTGGCACAATCTT TTTATTTTTTTTTTGAGATGGAGTCTTGCTCTGTCACCCAGGCTGGAGTGCAGTGGCACAATCTT T C NUCKS1 Ensembl:ENSG00000069275 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1014561389 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24626121 20281 RMVar_ID_20281 Human_SNP_ID_47118152 A-to-I Human chr1 - 205736030 205736030 205736030 GGAGAATTGCTTGAGTCCAGGAGTTTGAGGCTATAGTGAGCTATGGTCACACCACTGCACTTCAT GGAGAATTGCTTGAGTCCAGGAGTTTGAGGCTGTAGTGAGCTATGGTCACACCACTGCACTTCAT T C NUCKS1 Ensembl:ENSG00000069275 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs939612668 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5744337,Human_RBP_ID_10741551 20282 RMVar_ID_20282 Human_SNP_ID_47118153 A-to-I Human chr1 - 205736030 205736030 205736030 GGAGAATTGCTTGAGTCCAGGAGTTTGAGGCTATAGTGAGCTATGGTCACACCACTGCACTTCAT GGAGAATTGCTTGAGTCCAGGAGTTTGAGGCTCTAGTGAGCTATGGTCACACCACTGCACTTCAT T G NUCKS1 Ensembl:ENSG00000069275 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs939612668 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5744337,Human_RBP_ID_10741551 20283 RMVar_ID_20283 Human_SNP_ID_47118183 A-to-I Human chr1 - 205736184 205736182 205736184 ACTTTGAGAGGCCGAGAAGGGAGGATCACTTGAGGCCAGGAGTTCAAAACCAGCCTGGGAAACAG ACTTTGAGAGGCCGAGAAGGGAGGATCACTTG__GCCAGGAGTTCAAAACCAGCCTGGGAAACAG CCT C NUCKS1 Ensembl:ENSG00000069275 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879513145 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_18560813 20284 RMVar_ID_20284 Human_SNP_ID_47118193 A-to-I Human chr1 - 205736233 205736233 205736233 ATAAAAATAGGGAGGGCTGGATGTGGTGGCTCATGCTTGTAATCCTAGCACTTTGAGAGGCCGAG ATAAAAATAGGGAGGGCTGGATGTGGTGGCTCGTGCTTGTAATCCTAGCACTTTGAGAGGCCGAG T C NUCKS1 Ensembl:ENSG00000069275 Protein coding intron GSE38233;GSE107867 cultured B-cells;ASD brains,cerebellum - 24183664,30559470 RNA-Seq:(High) rs1332867244 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_223561 20285 RMVar_ID_20285 Human_SNP_ID_47118313 A-to-I Human chr1 - 205736768 205736768 205736768 GGAGTGCAGTGGCGTGATCTCGGCTCACTGCAAACTCCGTTCCCCGGGTTCAAGCTATTCTCCTG GGAGTGCAGTGGCGTGATCTCGGCTCACTGCATACTCCGTTCCCCGGGTTCAAGCTATTCTCCTG T A NUCKS1 Ensembl:ENSG00000069275 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1013596759 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10741591 20286 RMVar_ID_20286 Human_SNP_ID_47118749 A-to-I Human chr1 - 205738821 205738821 205738821 GCACTGCAACCTCCGCCTCCCAGGCTCAAGCTATTCTCCCACCTCAGCCCCTGGAGTGGCTGGGA GCACTGCAACCTCCGCCTCCCAGGCTCAAGCTGTTCTCCCACCTCAGCCCCTGGAGTGGCTGGGA T C NUCKS1 Ensembl:ENSG00000069275 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006246382 Functional Loss SNV dbSNP153 33..33 33 - - - 20287 RMVar_ID_20287 Human_SNP_ID_47118772 A-to-I Human chr1 - 205738904 205738904 205738904 ATTTAAATTTTATGTAGTTATTCATTTGAGACAGGTTCTCCCTCTCTCACCCAGGCCAGAGTGCA ATTTAAATTTTATGTAGTTATTCATTTGAGACCGGTTCTCCCTCTCTCACCCAGGCCAGAGTGCA T G NUCKS1 Ensembl:ENSG00000069275 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs926226397 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2117154,Human_RBP_ID_17557409 20288 RMVar_ID_20288 Human_SNP_ID_47119115 A-to-I Human chr1 - 205740167 205740167 205740167 AACCCCTTCTCTACTAAACTTAAAAAAAAATTAGCCAGCTGTGGTGGTGCACAACTGTAATCCCA AACCCCTTCTCTACTAAACTTAAAAAAAAATTTGCCAGCTGTGGTGGTGCACAACTGTAATCCCA T A NUCKS1 Ensembl:ENSG00000069275 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs982492114 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19258513 20289 RMVar_ID_20289 Human_SNP_ID_47119169 A-to-I Human chr1 - 205740397 205740397 205740397 CAGGCTGGTCTTGAACTCCTGGGACTCAAGCAATCCTGCCATCTCTGCCTCCCAGAGTGCTGGGA CAGGCTGGTCTTGAACTCCTGGGACTCAAGCAGTCCTGCCATCTCTGCCTCCCAGAGTGCTGGGA T C NUCKS1 Ensembl:ENSG00000069275 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1468659496 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8045735,Human_RBP_ID_23146283 20290 RMVar_ID_20290 Human_SNP_ID_47119171 A-to-I Human chr1 - 205740401 205740401 205740401 GGTTCAGGCTGGTCTTGAACTCCTGGGACTCAAGCAATCCTGCCATCTCTGCCTCCCAGAGTGCT GGTTCAGGCTGGTCTTGAACTCCTGGGACTCAGGCAATCCTGCCATCTCTGCCTCCCAGAGTGCT T C NUCKS1 Ensembl:ENSG00000069275 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs957940514 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8045735,Human_RBP_ID_23146283 20291 RMVar_ID_20291 Human_SNP_ID_47120391 A-to-I Human chr1 - 205744725 205744725 205744725 AGGAGGCTGAGGCAGGAGAATCGCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCCGAGACCACG AGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGGGAGGCGGAGGTTGCAGTGAGCCGAGACCACG T C NUCKS1 Ensembl:ENSG00000069275 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1297669024 Functional Loss SNV dbSNP153 33..33 33 - - - 20292 RMVar_ID_20292 Human_SNP_ID_47120394 A-to-I Human chr1 - 205744729 205744729 205744729 ACTTAGGAGGCTGAGGCAGGAGAATCGCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCCGAGAC ACTTAGGAGGCTGAGGCAGGAGAATCGCTTGACCCCAGGAGGCGGAGGTTGCAGTGAGCCGAGAC T G NUCKS1 Ensembl:ENSG00000069275 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs949681290 Functional Loss SNV dbSNP153 33..33 33 - - - 20293 RMVar_ID_20293 Human_SNP_ID_47120576 A-to-I Human chr1 - 205745367 205745367 205745367 CTCCCACCTCAGCCTTTCAGGTAGCTGGGACTATAGGTGTGGCCCACCACGCCTGGCTAATTTTT CTCCCACCTCAGCCTTTCAGGTAGCTGGGACTGTAGGTGTGGCCCACCACGCCTGGCTAATTTTT T C NUCKS1 Ensembl:ENSG00000069275 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs561720509 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5744467,Human_RBP_ID_10742021 20294 RMVar_ID_20294 Human_SNP_ID_47126747 A-to-I Human chr1 - 205769566 205769566 205769566 AAATTAGCCAGGCGTGATGGCACGTGTCTGTAATCCCAGCTACTCTGGAGACTGAGGTGGGAGAA AAATTAGCCAGGCGTGATGGCACGTGTCTGTAGTCCCAGCTACTCTGGAGACTGAGGTGGGAGAA T C RAB29 Ensembl:ENSG00000117280 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1485592663 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10742372 RMVar_hsa_circ_139232,RMVar_hsa_circ_102294 20295 RMVar_ID_20295 Human_SNP_ID_47139922 A-to-I Human chr1 + 205824923 205824923 205824923 ATTTTTGTATTTTTAGTAGAGACGGTCTTGCCATGTTGGCGAGGCTGGTCTCAAACTCTGACCAC ATTTTTGTATTTTTAGTAGAGACGGTCTTGCCGTGTTGGCGAGGCTGGTCTCAAACTCTGACCAC A G AC119673.3 Ensembl:ENSG00000286619 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031949054 Functional Loss SNV dbSNP153 33..33 33 - - - 20296 RMVar_ID_20296 Human_SNP_ID_47139923 A-to-I Human chr1 + 205824923 205824923 205824923 ATTTTTGTATTTTTAGTAGAGACGGTCTTGCCATGTTGGCGAGGCTGGTCTCAAACTCTGACCAC ATTTTTGTATTTTTAGTAGAGACGGTCTTGCCTTGTTGGCGAGGCTGGTCTCAAACTCTGACCAC A T AC119673.3 Ensembl:ENSG00000286619 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031949054 Functional Loss SNV dbSNP153 33..33 33 - - - 20297 RMVar_ID_20297 Human_SNP_ID_47278359 A-to-I Human chr1 + 206444139 206444139 206444139 TTGAACCCAGGAGGCAGAGGCCTCAGTGAGCCAAGATTGTACCACTGTAACCCAGACAGGCGACT TTGAACCCAGGAGGCAGAGGCCTCAGTGAGCCCAGATTGTACCACTGTAACCCAGACAGGCGACT A C SRGAP2 Ensembl:ENSG00000266028 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1311497095 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17825,RMVar_hsa_circ_1893,RMVar_hsa_circ_60834,RMVar_hsa_circ_69076,RMVar_hsa_circ_21473,RMVar_hsa_circ_19938,RMVar_hsa_circ_22349 20298 RMVar_ID_20298 Human_SNP_ID_47290308 A-to-I Human chr1 + 206489666 206489666 206489666 GGGAGTTCGAGACTGCAGTGAGCTAAGATCACACCACTGCAGCACTCCAGCCAGGGCAAGAGCGA GGGAGTTCGAGACTGCAGTGAGCTAAGATCACTCCACTGCAGCACTCCAGCCAGGGCAAGAGCGA A T IKBKE Ensembl:ENSG00000263528 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1206079680 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_353224,RMVar_hsa_circ_318636 20299 RMVar_ID_20299 Human_SNP_ID_47329756 A-to-I Human chr1 + 206653279 206653279 206653279 GGCTCAAGTGATCCATGTGCCTTACCCTCTCAAAGTGCTGGGATTATAGGTGTGAGCGACCGTGC GGCTCAAGTGATCCATGTGCCTTACCCTCTCAGAGTGCTGGGATTATAGGTGTGAGCGACCGTGC A G DYRK3 Ensembl:ENSG00000143479 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1315762990 Functional Loss SNV dbSNP153 33..33 33 - - - 20300 RMVar_ID_20300 Human_SNP_ID_47339748 A-to-I Human chr1 - 206696095 206696095 206696095 CTGGCAAAGAAATCATCTGCCGTGTGACTGGTAGGATGAAGGTGAAGGCAGGTGAGATGAATCCT CTGGCAAAGAAATCATCTGCCGTGTGACTGGTGGGATGAAGGTGAAGGCAGGTGAGATGAATCCT T C AL591846.2 Ensembl:ENSG00000224114 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879954703 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1839027 20301 RMVar_ID_20301 Human_SNP_ID_47339754 A-to-I Human chr1 + 206696115 206696115 206696115 TCACCTTCATCCTACCAGTCACACGGCAGATGATTTCTTTGCCAGAAAGATCAGTGACATGGACA TCACCTTCATCCTACCAGTCACACGGCAGATGGTTTCTTTGCCAGAAAGATCAGTGACATGGACA A G MAPKAPK2 Ensembl:ENSG00000162889 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879976912 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99465,RMVar_hsa_circ_139257 20302 RMVar_ID_20302 Human_SNP_ID_47438158 A-to-I Human chr1 + 207094242 207094242 207094242 GCATACCTGCAGTCCCAGCTACTTGGGAAGCTAAGGCAGGAGGATAGCTTGAGTCCAGAAATTTG GCATACCTGCAGTCCCAGCTACTTGGGAAGCTGAGGCAGGAGGATAGCTTGAGTCCAGAAATTTG A G C4BPB Ensembl:ENSG00000123843 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1138016 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82656,RMVar_hsa_circ_139287 20303 RMVar_ID_20303 Human_SNP_ID_47441707 A-to-I Human chr1 + 207108920 207108920 207108920 AATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTAGTCAGGCCGGTCTTGAACTCCTGA AATTTTTGTATTTTTAGTAGAGACGGGGTTTCGCCATGTTAGTCAGGCCGGTCTTGAACTCCTGA A G C4BPA Ensembl:ENSG00000123838 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1198809556 Functional Loss SNV dbSNP153 33..33 33 - - - 20304 RMVar_ID_20304 Human_SNP_ID_47441712 A-to-I Human chr1 + 207108932 207108932 207108932 TTTAGTAGAGACGGGGTTTCACCATGTTAGTCAGGCCGGTCTTGAACTCCTGACCTCGTGATCTG TTTAGTAGAGACGGGGTTTCACCATGTTAGTCGGGCCGGTCTTGAACTCCTGACCTCGTGATCTG A G C4BPA Ensembl:ENSG00000123838 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs923465902 Functional Loss SNV dbSNP153 33..33 33 - - - 20305 RMVar_ID_20305 Human_SNP_ID_47498559 A-to-I Human chr1 + 207360222 207360221 207360223 TGAAAGACTGAATCTTCCTTTGTTGCACAAATAGAGTTTGGAAAAAGCCTGTGAAAGGTGTCTTC TGAAAGACTGAATCTTCCTTTGTTGCACAAAT__AGTTTGGAAAAAGCCTGTGAAAGGTGTCTTC TAG T CD55 Ensembl:ENSG00000196352 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs752470521 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_339576,Human_RBP_ID_2118486,Human_RBP_ID_8296422,Human_RBP_ID_17181313,Human_RBP_ID_17580712,Human_RBP_ID_23206271,Human_RBP_ID_23359198,Human_RBP_ID_26374938 RMVar_hsa_circ_94382,RMVar_hsa_circ_139296 20306 RMVar_ID_20306 Human_SNP_ID_47498560 A-to-I Human chr1 + 207360222 207360222 207360222 TGAAAGACTGAATCTTCCTTTGTTGCACAAATAGAGTTTGGAAAAAGCCTGTGAAAGGTGTCTTC TGAAAGACTGAATCTTCCTTTGTTGCACAAATGGAGTTTGGAAAAAGCCTGTGAAAGGTGTCTTC A G CD55 Ensembl:ENSG00000196352 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1467997572 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_339576,Human_RBP_ID_2118486,Human_RBP_ID_8296422,Human_RBP_ID_17181313,Human_RBP_ID_17580712,Human_RBP_ID_23206271,Human_RBP_ID_23359198,Human_RBP_ID_26374938 RMVar_hsa_circ_94382,RMVar_hsa_circ_139296 20307 RMVar_ID_20307 Human_SNP_ID_47590172 A-to-I Human chr1 + 207768991 207768991 207768991 ATTAAGATACCTTCTTATAGGCTGGGTGGGGTAGCTCACACCTGTAATACCAGAACTTTGGGAGG ATTAAGATACCTTCTTATAGGCTGGGTGGGGTGGCTCACACCTGTAATACCAGAACTTTGGGAGG A G CD46 Ensembl:ENSG00000117335 Protein coding intron GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459,32596459 RNA-Seq:(High) rs907336419 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557413 RMVar_hsa_circ_307897,RMVar_hsa_circ_342330,RMVar_hsa_circ_139308,RMVar_hsa_circ_45582,RMVar_hsa_circ_91318,RMVar_hsa_circ_65202,RMVar_hsa_circ_323980,RMVar_hsa_circ_114012,RMVar_hsa_circ_139312,RMVar_hsa_circ_97265,RMVar_hsa_circ_139313,RMVar_hsa_circ_139314 20308 RMVar_ID_20308 Human_SNP_ID_47590180 A-to-I Human chr1 + 207769012 207769012 207769012 CTGGGTGGGGTAGCTCACACCTGTAATACCAGAACTTTGGGAGGCCGAGGTGGGTGGATCACGAG CTGGGTGGGGTAGCTCACACCTGTAATACCAGCACTTTGGGAGGCCGAGGTGGGTGGATCACGAG A C CD46 Ensembl:ENSG00000117335 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1212487666 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557413,Human_RBP_ID_24756596 RMVar_hsa_circ_307897,RMVar_hsa_circ_342330,RMVar_hsa_circ_139308,RMVar_hsa_circ_45582,RMVar_hsa_circ_91318,RMVar_hsa_circ_65202,RMVar_hsa_circ_323980,RMVar_hsa_circ_114012,RMVar_hsa_circ_139312,RMVar_hsa_circ_97265,RMVar_hsa_circ_139313,RMVar_hsa_circ_139314 20309 RMVar_ID_20309 Human_SNP_ID_47590190 A-to-I Human chr1 + 207769062 207769062 207769062 TGGGTGGATCACGAGGTCAGAAGTTCAAGACCAGCCTGGCTAAGTTGGTGAAACCCCATCTCTAC TGGGTGGATCACGAGGTCAGAAGTTCAAGACCGGCCTGGCTAAGTTGGTGAAACCCCATCTCTAC A G CD46 Ensembl:ENSG00000117335 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs561938965 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_307897,RMVar_hsa_circ_342330,RMVar_hsa_circ_139308,RMVar_hsa_circ_45582,RMVar_hsa_circ_91318,RMVar_hsa_circ_65202,RMVar_hsa_circ_323980,RMVar_hsa_circ_114012,RMVar_hsa_circ_139312,RMVar_hsa_circ_97265,RMVar_hsa_circ_139313,RMVar_hsa_circ_139314 20310 RMVar_ID_20310 Human_SNP_ID_47590200 A-to-I Human chr1 + 207769127 207769127 207769127 TAAAAATACAAAAATTAGCGGGGTGCGGTGGCAGGCACTTGTAATCCCAGCTGCTCGGGAGGCCG TAAAAATACAAAAATTAGCGGGGTGCGGTGGCGGGCACTTGTAATCCCAGCTGCTCGGGAGGCCG A G CD46 Ensembl:ENSG00000117335 Protein coding intron GSE47997;GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831 K562 cells&HepG2 cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line - 23474544,29129909,32596459 RNA-Seq:(High) rs1409903107 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_307897,RMVar_hsa_circ_342330,RMVar_hsa_circ_139308,RMVar_hsa_circ_45582,RMVar_hsa_circ_91318,RMVar_hsa_circ_65202,RMVar_hsa_circ_323980,RMVar_hsa_circ_114012,RMVar_hsa_circ_139312,RMVar_hsa_circ_97265,RMVar_hsa_circ_139313,RMVar_hsa_circ_139314 20311 RMVar_ID_20311 Human_SNP_ID_47590212 A-to-I Human chr1 + 207769164 207769164 207769164 CTTGTAATCCCAGCTGCTCGGGAGGCCGAGGCAGGAGAATCGCTTGAACCCAGTGGGCAGAGGTT CTTGTAATCCCAGCTGCTCGGGAGGCCGAGGCGGGAGAATCGCTTGAACCCAGTGGGCAGAGGTT A G CD46 Ensembl:ENSG00000117335 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1289740344 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_307897,RMVar_hsa_circ_342330,RMVar_hsa_circ_139308,RMVar_hsa_circ_45582,RMVar_hsa_circ_91318,RMVar_hsa_circ_65202,RMVar_hsa_circ_323980,RMVar_hsa_circ_114012,RMVar_hsa_circ_139312,RMVar_hsa_circ_97265,RMVar_hsa_circ_139313,RMVar_hsa_circ_139314 20312 RMVar_ID_20312 Human_SNP_ID_47590220 A-to-I Human chr1 + 207769183 207769183 207769183 GGGAGGCCGAGGCAGGAGAATCGCTTGAACCCAGTGGGCAGAGGTTGCAGTGAGCCAAGATCATG GGGAGGCCGAGGCAGGAGAATCGCTTGAACCCGGTGGGCAGAGGTTGCAGTGAGCCAAGATCATG A G CD46 Ensembl:ENSG00000117335 Protein coding intron GSE47997;GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,29129909,32596459 RNA-Seq:(High) rs1451606011 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_307897,RMVar_hsa_circ_342330,RMVar_hsa_circ_139308,RMVar_hsa_circ_45582,RMVar_hsa_circ_91318,RMVar_hsa_circ_65202,RMVar_hsa_circ_323980,RMVar_hsa_circ_114012,RMVar_hsa_circ_139312,RMVar_hsa_circ_97265,RMVar_hsa_circ_139313,RMVar_hsa_circ_139314 20313 RMVar_ID_20313 Human_SNP_ID_47590229 A-to-I Human chr1 + 207769240 207769239 207769241 AGATCATGCCACTGCACTCCAGCCTGGGTGACAGAGTGAGACTCTGTCTCAAAACAAAAACCTTC AGATCATGCCACTGCACTCCAGCCTGGGTGAC__AGTGAGACTCTGTCTCAAAACAAAAACCTTC CAG C CD46 Ensembl:ENSG00000117335 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1257356158 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_23146308 RMVar_hsa_circ_307897,RMVar_hsa_circ_342330,RMVar_hsa_circ_139308,RMVar_hsa_circ_45582,RMVar_hsa_circ_91318,RMVar_hsa_circ_65202,RMVar_hsa_circ_323980,RMVar_hsa_circ_114012,RMVar_hsa_circ_139312,RMVar_hsa_circ_97265,RMVar_hsa_circ_139313,RMVar_hsa_circ_139314 20314 RMVar_ID_20314 Human_SNP_ID_47590350 A-to-I Human chr1 + 207769782 207769782 207769782 TACCCCAAGCACATTCCCTTTTTTTTTTTTTGAGACAGAGTCTTGCTCTGTCACCCAGGATGGCG TACCCCAAGCACATTCCCTTTTTTTTTTTTTGTGACAGAGTCTTGCTCTGTCACCCAGGATGGCG A T CD46 Ensembl:ENSG00000117335 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1268923394 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_307897,RMVar_hsa_circ_342330,RMVar_hsa_circ_139308,RMVar_hsa_circ_45582,RMVar_hsa_circ_91318,RMVar_hsa_circ_65202,RMVar_hsa_circ_323980,RMVar_hsa_circ_114012,RMVar_hsa_circ_139312,RMVar_hsa_circ_97265,RMVar_hsa_circ_139313,RMVar_hsa_circ_139314 20315 RMVar_ID_20315 Human_SNP_ID_47590397 A-to-I Human chr1 + 207769915 207769915 207769915 AGACTCCCAAGTAGCTGGTATTACAGGCACCCACCACTATGCCGGCTAATTTTTTGTATTTTTAG AGACTCCCAAGTAGCTGGTATTACAGGCACCCGCCACTATGCCGGCTAATTTTTTGTATTTTTAG A G CD46 Ensembl:ENSG00000117335 Protein coding intron GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831 HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line - 29129909,32596459 RNA-Seq:(High) rs916030192 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_307897,RMVar_hsa_circ_342330,RMVar_hsa_circ_139308,RMVar_hsa_circ_45582,RMVar_hsa_circ_91318,RMVar_hsa_circ_65202,RMVar_hsa_circ_323980,RMVar_hsa_circ_114012,RMVar_hsa_circ_139312,RMVar_hsa_circ_97265,RMVar_hsa_circ_139313,RMVar_hsa_circ_139314 20316 RMVar_ID_20316 Human_SNP_ID_47590403 A-to-I Human chr1 + 207769930 207769930 207769930 TGGTATTACAGGCACCCACCACTATGCCGGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTC TGGTATTACAGGCACCCACCACTATGCCGGCTGATTTTTTGTATTTTTAGTAGAGACGGGGTTTC A G CD46 Ensembl:ENSG00000117335 Protein coding intron GSE47997;GSE38233;GSE38233;GSE100210;GSE100210;GSE99789;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;cultured B-cells;HepG2 cell line;HepG2 cell line;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,24183664,29129909,29129909,29796672,32596459 RNA-Seq:(High) rs1170434070 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_307897,RMVar_hsa_circ_342330,RMVar_hsa_circ_139308,RMVar_hsa_circ_45582,RMVar_hsa_circ_91318,RMVar_hsa_circ_65202,RMVar_hsa_circ_323980,RMVar_hsa_circ_114012,RMVar_hsa_circ_139312,RMVar_hsa_circ_97265,RMVar_hsa_circ_139313,RMVar_hsa_circ_139314 20317 RMVar_ID_20317 Human_SNP_ID_47590419 A-to-I Human chr1 + 207769980 207769980 207769980 TAGAGACGGGGTTTCTCCATGATGGCCTGGCTAGTCTCGAACTCCTGACCTCAAGTGATTCACCT TAGAGACGGGGTTTCTCCATGATGGCCTGGCTGGTCTCGAACTCCTGACCTCAAGTGATTCACCT A G CD46 Ensembl:ENSG00000117335 Protein coding intron GSE38233;GSE100210;GSE99789;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;ASD brains,frontal_cortex;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,29796672,30559470,31158229,31158229,31158229,32596459,32596459 RNA-Seq:(High) rs1217016086 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557414 RMVar_hsa_circ_307897,RMVar_hsa_circ_342330,RMVar_hsa_circ_139308,RMVar_hsa_circ_45582,RMVar_hsa_circ_91318,RMVar_hsa_circ_65202,RMVar_hsa_circ_323980,RMVar_hsa_circ_114012,RMVar_hsa_circ_139312,RMVar_hsa_circ_97265,RMVar_hsa_circ_139313,RMVar_hsa_circ_139314 20318 RMVar_ID_20318 Human_SNP_ID_47594406 A-to-I Human chr1 + 207787272 207787272 207787272 TGTTGTACCTGTACTAGAGATGGGGTTTCACCATGTTGGTCAGGCTGGTCTTGAACTCCTGACCT TGTTGTACCTGTACTAGAGATGGGGTTTCACCGTGTTGGTCAGGCTGGTCTTGAACTCCTGACCT A G CD46 Ensembl:ENSG00000117335 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1310749817 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_357352 20319 RMVar_ID_20319 Human_SNP_ID_47594425 A-to-I Human chr1 + 207787352 207787352 207787352 CCTCGGCCTCCCAAGGTGCTAGGATTACAGGCATGAGCCACCGCGCCCGGCCTTAATGGGTCTTT CCTCGGCCTCCCAAGGTGCTAGGATTACAGGCGTGAGCCACCGCGCCCGGCCTTAATGGGTCTTT A G CD46 Ensembl:ENSG00000117335 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs558909542 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24627561 RMVar_hsa_circ_357352 20320 RMVar_ID_20320 Human_SNP_ID_47594426 A-to-I Human chr1 + 207787352 207787352 207787352 CCTCGGCCTCCCAAGGTGCTAGGATTACAGGCATGAGCCACCGCGCCCGGCCTTAATGGGTCTTT CCTCGGCCTCCCAAGGTGCTAGGATTACAGGCTTGAGCCACCGCGCCCGGCCTTAATGGGTCTTT A T CD46 Ensembl:ENSG00000117335 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs558909542 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24627561 RMVar_hsa_circ_357352 20321 RMVar_ID_20321 Human_SNP_ID_47878219 A-to-I Human chr1 - 208962934 208962934 208962934 AACTAAAAATAGAACTACCATACAATTTAGCAATCCTACTTCTGGGTATTTATCCATAGGAAAGG AACTAAAAATAGAACTACCATACAATTTAGCAGTCCTACTTCTGGGTATTTATCCATAGGAAAGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs753060831 Functional Loss SNV dbSNP153 33..33 33 - - - 20322 RMVar_ID_20322 Human_SNP_ID_47878520 A-to-I Human chr1 - 208964196 208964196 208964196 ACAGACATAGCAAAAACAATCCTAAAATTTATATGTAACCACAAAAGACCACGAATAGCCAAAGG ACAGACATAGCAAAAACAATCCTAAAATTTATGTGTAACCACAAAAGACCACGAATAGCCAAAGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1286303866 Functional Loss SNV dbSNP153 33..33 33 - - - 20323 RMVar_ID_20323 Human_SNP_ID_47895785 A-to-I Human chr1 - 209033849 209033849 209033849 TTCTCGCTCCTTCTTTGCCTTCCGCCACGATTATAAGTTTCCTGAAGCCTTCCCAGTAGCCAAGC TTCTCGCTCCTTCTTTGCCTTCCGCCACGATTGTAAGTTTCCTGAAGCCTTCCCAGTAGCCAAGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992058866 Functional Loss SNV dbSNP153 33..33 33 - - - 20324 RMVar_ID_20324 Human_SNP_ID_47943769 A-to-I Human chr1 - 209230003 209230003 209230003 CCGAAGAAGTGAAAGATCTTGGAATGAAAACTATAAAACACCAATGAATGAAATTGAAGAGGACA CCGAAGAAGTGAAAGATCTTGGAATGAAAACTGTAAAACACCAATGAATGAAATTGAAGAGGACA T C AC092810.3 Ensembl:ENSG00000232537 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1248588928 Functional Loss SNV dbSNP153 33..33 33 - - - 20325 RMVar_ID_20325 Human_SNP_ID_48035893 A-to-I Human chr1 - 209614960 209614960 209614960 GCCTTTAGTTCTCCACTGGGGAGGAATCCTGGACCAAGCACAAAAACTTAACAAAAGTGATGTAA GCCTTTAGTTCTCCACTGGGGAGGAATCCTGGGCCAAGCACAAAAACTTAACAAAAGTGATGTAA T C LAMB3 Ensembl:ENSG00000196878 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1469897684 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8296648,Human_RBP_ID_27393382 Human_miRNA_ID_244923,Human_miRNA_ID_247427,Human_miRNA_ID_2033593,Human_miRNA_ID_2034897,Human_miRNA_ID_2235890 RMVar_hsa_circ_139336,RMVar_hsa_circ_90245 20326 RMVar_ID_20326 Human_SNP_ID_170066771 A-to-I Human chr4 + 134420 134420 134420 CCACCTCGGCCTCCCAAAGTGCTGGGGATTACAGGCGTGAGCCACCGTGCCCAGCCAATCAGTGT CCACCTCGGCCTCCCAAAGTGCTGGGGATTACGGGCGTGAGCCACCGTGCCCAGCCAATCAGTGT A G ZNF718 Ensembl:ENSG00000250312 Protein coding intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1318170773 Functional Loss SNV dbSNP153 33..33 33 - - - 20327 RMVar_ID_20327 Human_SNP_ID_170154756 A-to-I Human chr4 - 456085 456085 456085 GCCTGGGTGACAGGGCGAGACTCCATCTCAATAAATAAATAAATAAATAAATAAATAAATAAATA GCCTGGGTGACAGGGCGAGACTCCATCTCAATCAATAAATAAATAAATAAATAAATAAATAAATA T G ZNF721,ABCA11P Ensembl:ENSG00000182903,Ensembl:ENSG00000251595 Protein coding,Pseudogene intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1400132232 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17410457 RMVar_hsa_circ_7073 20328 RMVar_ID_20328 Human_SNP_ID_170156976 A-to-I Human chr4 - 464823 464823 464823 CTCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCCCAGCCCCAGCTG CTCCCGCCTCGGCCTCCCAAAGTGCTGGGATTGCAGGCGTGAGCCACCGCGCCCAGCCCCAGCTG T C ZNF721,ABCA11P Ensembl:ENSG00000182903,Ensembl:ENSG00000251595 Protein coding,Pseudogene intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1273422435 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7073 20329 RMVar_ID_20329 Human_SNP_ID_170157092 A-to-I Human chr4 - 465132 465132 465132 GAAATCCACCTGCCATGGCCTCCCAAAGTGCTAGGTTTACAGGCATGTATCATCAGGCCCAGCTG GAAATCCACCTGCCATGGCCTCCCAAAGTGCTGGGTTTACAGGCATGTATCATCAGGCCCAGCTG T C ZNF721,ABCA11P Ensembl:ENSG00000182903,Ensembl:ENSG00000251595 Protein coding,Pseudogene intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs979183811 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7313582,Human_RBP_ID_18517965 RMVar_hsa_circ_7073 20330 RMVar_ID_20330 Human_SNP_ID_170157093 A-to-I Human chr4 - 465132 465132 465132 GAAATCCACCTGCCATGGCCTCCCAAAGTGCTAGGTTTACAGGCATGTATCATCAGGCCCAGCTG GAAATCCACCTGCCATGGCCTCCCAAAGTGCTCGGTTTACAGGCATGTATCATCAGGCCCAGCTG T G ZNF721,ABCA11P Ensembl:ENSG00000182903,Ensembl:ENSG00000251595 Protein coding,Pseudogene intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs979183811 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7313582,Human_RBP_ID_18517965 RMVar_hsa_circ_7073 20331 RMVar_ID_20331 Human_SNP_ID_170157129 A-to-I Human chr4 - 465262 465262 465262 CCATCTCAGCCTCCCAAGTAGCTGGGAATACAAGTACACGCCACCAGGTCCAGCTAAGTTTTTTG CCATCTCAGCCTCCCAAGTAGCTGGGAATACAGGTACACGCCACCAGGTCCAGCTAAGTTTTTTG T C ZNF721,ABCA11P Ensembl:ENSG00000182903,Ensembl:ENSG00000251595 Protein coding,Pseudogene intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1005633603 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5250332,Human_RBP_ID_18517966 RMVar_hsa_circ_7073 20332 RMVar_ID_20332 Human_SNP_ID_170157130 A-to-I Human chr4 - 465262 465262 465262 CCATCTCAGCCTCCCAAGTAGCTGGGAATACAAGTACACGCCACCAGGTCCAGCTAAGTTTTTTG CCATCTCAGCCTCCCAAGTAGCTGGGAATACACGTACACGCCACCAGGTCCAGCTAAGTTTTTTG T G ZNF721,ABCA11P Ensembl:ENSG00000182903,Ensembl:ENSG00000251595 Protein coding,Pseudogene intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1005633603 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5250332,Human_RBP_ID_18517966 RMVar_hsa_circ_7073 20333 RMVar_ID_20333 Human_SNP_ID_170157816 A-to-I Human chr4 - 467741 467741 467741 AACTGAGTCACAGGGCTGCTTCAAGGAGCACAACTGAGGCCAGGATCTGCAGGCCTGCCTCCAGG AACTGAGTCACAGGGCTGCTTCAAGGAGCACAGCTGAGGCCAGGATCTGCAGGCCTGCCTCCAGG T C ZNF721,ABCA11P Ensembl:ENSG00000182903,Ensembl:ENSG00000251595 Protein coding,Pseudogene intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs959271413 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5211705,Human_RBP_ID_15162966,Human_RBP_ID_21989446 RMVar_hsa_circ_7073 20334 RMVar_ID_20334 Human_SNP_ID_170158480 A-to-I Human chr4 - 470154 470154 470154 ACTTTTGCCAGGCACAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCAGAGGCAGGTGGA ACTTTTGCCAGGCACAGTGGCTCACGCCTGTAGTCCCAGCACTTTGGGAGGCAGAGGCAGGTGGA T C ZNF721,ABCA11P Ensembl:ENSG00000182903,Ensembl:ENSG00000251595 Protein coding,Pseudogene intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1553867391 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17410089,Human_RBP_ID_23191067 RMVar_hsa_circ_7073 20335 RMVar_ID_20335 Human_SNP_ID_170162069 A-to-I Human chr4 - 483440 483440 483440 TCAAGGGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAAGCACTCACCACCATGCCCA TCAAGGGATTCTCCTGCCTCAGCCTCCCAAGTCGCTGGGATTACAAGCACTCACCACCATGCCCA T G ZNF721 Ensembl:ENSG00000182903 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs782489129 Functional Loss SNV dbSNP153 33..33 33 - - - 20336 RMVar_ID_20336 Human_SNP_ID_170162071 A-to-I Human chr4 - 483443 483443 483443 GGTTCAAGGGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAAGCACTCACCACCATGC GGTTCAAGGGATTCTCCTGCCTCAGCCTCCCAGGTAGCTGGGATTACAAGCACTCACCACCATGC T C ZNF721 Ensembl:ENSG00000182903 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1335201223 Functional Loss SNV dbSNP153 33..33 33 - - - 20337 RMVar_ID_20337 Human_SNP_ID_170162189 A-to-I Human chr4 - 483923 483892 483924 CCTGGAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAATCCAGGAGGCTGAGGTT CCTGGAGTCCCAGCTACTCGGGAGGCTGAGG________________________________TT ACCTCAGCCTCCTGGATTCAAGCGATTCTCCTG A ZNF721 Ensembl:ENSG00000182903 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1553869877 Functional Loss DEL dbSNP153 32..63 33 - - - 20338 RMVar_ID_20338 Human_SNP_ID_170162207 A-to-I Human chr4 - 483987 483987 483987 ACCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATCAGCTGAGTGTGCTGGTACATCC ACCAACATGGTGAAACCCCGTCTCTACTAAAAGTACAAAAATCAGCTGAGTGTGCTGGTACATCC T C ZNF721 Ensembl:ENSG00000182903 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs540453619 Functional Loss SNV dbSNP153 33..33 33 - - - 20339 RMVar_ID_20339 Human_SNP_ID_170162746 A-to-I Human chr4 - 485923 485923 485923 GTCGCCAGGCTGGAGTGCAGTGGCACAATCTCAGCTCACTGCAACCTCTACCTCCTCGGTTCAAG GTCGCCAGGCTGGAGTGCAGTGGCACAATCTCGGCTCACTGCAACCTCTACCTCCTCGGTTCAAG T C ZNF721 Ensembl:ENSG00000182903 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1553870251 Functional Loss SNV dbSNP153 33..33 33 - - - 20340 RMVar_ID_20340 Human_SNP_ID_170163471 A-to-I Human chr4 - 488627 488627 488627 TGCGGTTTCACAGTGTTGGCCAGGATGGTCTCAATCTCTTCACCTTGTGATCCGCCTGCCTCGGC TGCGGTTTCACAGTGTTGGCCAGGATGGTCTCTATCTCTTCACCTTGTGATCCGCCTGCCTCGGC T A ZNF721 Ensembl:ENSG00000182903 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1486286744 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8592388 20341 RMVar_ID_20341 Human_SNP_ID_170164799 A-to-I Human chr4 - 493496 493496 493496 TTTTGTATTTTTAGTAAAGAAAGGGTTTCGCCATGTTGGCCAGGCTGGTCTTGAACTCCTGACCG TTTTGTATTTTTAGTAAAGAAAGGGTTTCGCCGTGTTGGCCAGGCTGGTCTTGAACTCCTGACCG T C ZNF721 Ensembl:ENSG00000182903 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs946213280 Functional Loss SNV dbSNP153 33..33 33 - - - 20342 RMVar_ID_20342 Human_SNP_ID_170164806 A-to-I Human chr4 - 493512 493512 493512 ACCATGCCCCACTAATTTTTGTATTTTTAGTAAAGAAAGGGTTTCGCCATGTTGGCCAGGCTGGT ACCATGCCCCACTAATTTTTGTATTTTTAGTACAGAAAGGGTTTCGCCATGTTGGCCAGGCTGGT T G ZNF721 Ensembl:ENSG00000182903 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1458082045 Functional Loss SNV dbSNP153 33..33 33 - - - 20343 RMVar_ID_20343 Human_SNP_ID_170166092 A-to-I Human chr4 - 497642 497642 497642 CCTCGTGATCCGCCCGCCTCTGTCTCCCAAAGAGCTGGGATTACAGGCGTGAGACACCGCGCCCT CCTCGTGATCCGCCCGCCTCTGTCTCCCAAAGTGCTGGGATTACAGGCGTGAGACACCGCGCCCT T A ZNF721 Ensembl:ENSG00000182903 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1553872580 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119534,RMVar_hsa_circ_224170 20344 RMVar_ID_20344 Human_SNP_ID_170166112 A-to-I Human chr4 - 497684 497684 497684 ACGGGTTTCACCATGTTAGCCAGGATGGTCTCAATCTCCTGACCTCGTGATCCGCCCGCCTCTGT ACGGGTTTCACCATGTTAGCCAGGATGGTCTCGATCTCCTGACCTCGTGATCCGCCCGCCTCTGT T C ZNF721 Ensembl:ENSG00000182903 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1553872618 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119534,RMVar_hsa_circ_224170 20345 RMVar_ID_20345 Human_SNP_ID_170166121 A-to-I Human chr4 - 497699 497699 497699 TATTTTTTAGTAGTGACGGGTTTCACCATGTTAGCCAGGATGGTCTCAATCTCCTGACCTCGTGA TATTTTTTAGTAGTGACGGGTTTCACCATGTTGGCCAGGATGGTCTCAATCTCCTGACCTCGTGA T C ZNF721 Ensembl:ENSG00000182903 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1375655213 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119534,RMVar_hsa_circ_224170 20346 RMVar_ID_20346 Human_SNP_ID_170166261 A-to-I Human chr4 - 498056 498056 498056 GGATTACAGGTGCGTGCCACCACGCACGGCTAATTTTTGTATTTTTAGTTGAGACGGGGTTTCAC GGATTACAGGTGCGTGCCACCACGCACGGCTACTTTTTGTATTTTTAGTTGAGACGGGGTTTCAC T G ZNF721 Ensembl:ENSG00000182903 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1426504653 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_161496 RMVar_hsa_circ_119534,RMVar_hsa_circ_224170 20347 RMVar_ID_20347 Human_SNP_ID_170166280 A-to-I Human chr4 - 498119 498119 498119 ATCACTGCAACCTCTGCCTCCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGG ATCACTGCAACCTCTGCCTCCCGGGTTCAAGCCATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGG T G ZNF721 Ensembl:ENSG00000182903 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1359852010 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119534,RMVar_hsa_circ_224170 20348 RMVar_ID_20348 Human_SNP_ID_170166281 A-to-I Human chr4 - 498122 498122 498122 CAGATCACTGCAACCTCTGCCTCCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCT CAGATCACTGCAACCTCTGCCTCCCGGGTTCACGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCT T G ZNF721 Ensembl:ENSG00000182903 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1288067510 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119534,RMVar_hsa_circ_224170 20349 RMVar_ID_20349 Human_SNP_ID_170166291 A-to-I Human chr4 - 498191 498187 498191 TTTTTTTTCTTTTTCTTTTCAGATGAAATCTCACTCTGTCGCCCAGGCTGGAATGCAGTGGCGTG TTTTTTTTCTTTTTCTTTTCAGATGAAATCTC____TGTCGCCCAGGCTGGAATGCAGTGGCGTG AGAGT A ZNF721 Ensembl:ENSG00000182903 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1177989554 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_7350744 RMVar_hsa_circ_119534,RMVar_hsa_circ_224170 20350 RMVar_ID_20350 Human_SNP_ID_170166547 A-to-I Human chr4 - 499013 499013 499013 TTAAAAAGTTTTTAATTTGGAAGGCAGGGTGCAGTGGCTCACGCCTTTAATCCCAGTACTTTGGG TTAAAAAGTTTTTAATTTGGAAGGCAGGGTGCGGTGGCTCACGCCTTTAATCCCAGTACTTTGGG T C ZNF721 Ensembl:ENSG00000182903 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1250184119 Functional Loss SNV dbSNP153 33..33 33 - - - 20351 RMVar_ID_20351 Human_SNP_ID_170170513 A-to-I Human chr4 + 512454 512454 512454 GGCCAGGCCGATCTCAAACTCCTGACCTTGTGATCTGCCCACCTCGGCCTCCCAACCATTATCAT GGCCAGGCCGATCTCAAACTCCTGACCTTGTGCTCTGCCCACCTCGGCCTCCCAACCATTATCAT A C PIGG Ensembl:ENSG00000174227 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1468520487 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69717,RMVar_hsa_circ_113243,RMVar_hsa_circ_22711,RMVar_hsa_circ_224173,RMVar_hsa_circ_367228,RMVar_hsa_circ_76495,RMVar_hsa_circ_224174,RMVar_hsa_circ_224175 20352 RMVar_ID_20352 Human_SNP_ID_170176214 A-to-I Human chr4 - 531520 531520 531520 GAGAGGCCCTGTAGGGACACAAAGAACTGCACATGCCTCCTGGGTACGAGACAGCGGACAGGCAG GAGAGGCCCTGTAGGGACACAAAGAACTGCACGTGCCTCCTGGGTACGAGACAGCGGACAGGCAG T C lnc-ZNF721-3 RNACentral:URS00008BC04F lincRNA intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1215440831 Functional Loss SNV dbSNP153 33..33 33 - - - 20353 RMVar_ID_20353 Human_SNP_ID_170198628 A-to-I Human chr4 + 609325 609325 609325 GACATGAACTCCTGGGCTGCAGTGATCCTCCTACCTCAGCTCCTGAGCAGCTGGGACCACAGGCA GACATGAACTCCTGGGCTGCAGTGATCCTCCTGCCTCAGCTCCTGAGCAGCTGGGACCACAGGCA A G AC116565.1 Ensembl:ENSG00000283183 lincRNA intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1014748252 Functional Loss SNV dbSNP153 33..33 33 - - - 20354 RMVar_ID_20354 Human_SNP_ID_170220150 A-to-I Human chr4 + 675865 675865 675865 CTTGGATCTGGATTGCGCTCTGGTGAGAATCTAATGCCTGATGAACTGAGGTGGAATAGTTTCAT CTTGGATCTGGATTGCGCTCTGGTGAGAATCTGATGCCTGATGAACTGAGGTGGAATAGTTTCAT A G MYL5 Ensembl:ENSG00000215375 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1183350542 Functional Loss SNV dbSNP153 33..33 33 - - - 20355 RMVar_ID_20355 Human_SNP_ID_170247515 A-to-I Human chr4 + 753253 753253 753253 TTGCCTAGGCTGGAGTATAGTGGTGCAATCTCAGCTCCCTGCAGCCTCGACCTCTTGGGCTCAAG TTGCCTAGGCTGGAGTATAGTGGTGCAATCTCGGCTCCCTGCAGCCTCGACCTCTTGGGCTCAAG A G PCGF3 Ensembl:ENSG00000185619 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1189677640 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 20356 RMVar_ID_20356 Human_SNP_ID_170254997 A-to-I Human chr4 - 770838 770838 770838 GTTAGCCAGGCTGGTCTCGAACTCCCGACTTCAGATGATCAGCCTGCCTTGGCCTCCTACGGTGC GTTAGCCAGGCTGGTCTCGAACTCCCGACTTCGGATGATCAGCCTGCCTTGGCCTCCTACGGTGC T C AC139887.2 Ensembl:ENSG00000249592 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1237159896 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15199387,Human_RBP_ID_24064157 20357 RMVar_ID_20357 Human_SNP_ID_170255788 A-to-I Human chr4 - 772679 772679 772679 GTGGTGAAACCCCGTCTCTACTAAAAACAAAAATTAGCCTGGCGTGGTGGCAGGTGCCTGTAATC GTGGTGAAACCCCGTCTCTACTAAAAACAAAAGTTAGCCTGGCGTGGTGGCAGGTGCCTGTAATC T C AC139887.2 Ensembl:ENSG00000249592 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1274714085 Functional Loss SNV dbSNP153 33..33 33 - - - 20358 RMVar_ID_20358 Human_SNP_ID_170256837 A-to-I Human chr4 - 775357 775357 775357 GCAACATGGCAAAACCCCATCTCTACAAAAATAAAAAATTAGCTGGGTGTGGTGGTGCCTGTAGT GCAACATGGCAAAACCCCATCTCTACAAAAATTAAAAATTAGCTGGGTGTGGTGGTGCCTGTAGT T A AC139887.2 Ensembl:ENSG00000249592 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1479415581 Functional Loss SNV dbSNP153 33..33 33 - - - 20359 RMVar_ID_20359 Human_SNP_ID_170257256 A-to-I Human chr4 - 776537 776537 776537 CCACCATGCCTGGCTAATTTTCTATTTTTTTTAATAGAGACGGGGTTTCTCCATGTTGGTCAAGC CCACCATGCCTGGCTAATTTTCTATTTTTTTTTATAGAGACGGGGTTTCTCCATGTTGGTCAAGC T A AC139887.2 Ensembl:ENSG00000249592 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1386534458 Functional Loss SNV dbSNP153 33..33 33 - - - 20360 RMVar_ID_20360 Human_SNP_ID_170257949 A-to-I Human chr4 - 778740 778740 778740 TACTCAGGAGGCTGAGACAGGAGAATTGCTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCTGAGA TACTCAGGAGGCTGAGACAGGAGAATTGCTTGTACCTGGGAGGCAGAGGTTGCAGTGAGCTGAGA T A AC139887.2 Ensembl:ENSG00000249592 lincRNA intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1250236269 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5250401 20361 RMVar_ID_20361 Human_SNP_ID_170258174 A-to-I Human chr4 - 779437 779426 779437 GTTGCCCAGGCTGGTCTTGAACTCCTGGGTTCAGGTGATCTTCCCACTTCAGCCTCCCAAAGTGC GTTGCCCAGGCTGGTCTTGAACTCCTGGGTTC___________CCACTTCAGCCTCCCAAAGTGC GGAAGATCACCT G AC139887.2 Ensembl:ENSG00000249592 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs531296487 Functional Loss DEL dbSNP153 33..43 33 - - - Human_RBP_ID_17574931 20362 RMVar_ID_20362 Human_SNP_ID_170258436 A-to-I Human chr4 - 780318 780318 780318 AGGTGTGGTGGCGCATGTCTGTAATCCCAGCTACTGGGGAAGCTGAGGCAGGAGAATCCCTTGAA AGGTGTGGTGGCGCATGTCTGTAATCCCAGCTGCTGGGGAAGCTGAGGCAGGAGAATCCCTTGAA T C AC139887.2 Ensembl:ENSG00000249592 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs755750456 Functional Loss SNV dbSNP153 33..33 33 - - - 20363 RMVar_ID_20363 Human_SNP_ID_170258448 A-to-I Human chr4 - 780362 780362 780362 CAACGTGGAGAAACCCCGTCTTTACTAAAAATACAAAATTAGCCAGGTGTGGTGGCGCATGTCTG CAACGTGGAGAAACCCCGTCTTTACTAAAAATGCAAAATTAGCCAGGTGTGGTGGCGCATGTCTG T C AC139887.2 Ensembl:ENSG00000249592 lincRNA intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs913653073 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10155160,Human_RBP_ID_23033637 20364 RMVar_ID_20364 Human_SNP_ID_170258478 A-to-I Human chr4 - 780465 780465 780465 ACAACACAGGCTGGGCGCGGTGGCTCACACCTATAATCCCAGCACTTTGGGAGGCAGAGGCGGGC ACAACACAGGCTGGGCGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCAGAGGCGGGC T C AC139887.2 Ensembl:ENSG00000249592 lincRNA intron GSE47997;GSE107867;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;ASD brains,cerebellum;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,30559470,31158229,32596459 RNA-Seq:(High) rs1047761684 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5103098,Human_RBP_ID_27070302 20365 RMVar_ID_20365 Human_SNP_ID_170268901 A-to-I Human chr4 - 813117 813117 813117 GGGACTACAGGCATCTGCCACCACACCCAGCTAATTTTTGCATTTTTAGTAGAGACGGGGTTTCA GGGACTACAGGCATCTGCCACCACACCCAGCTTATTTTTGCATTTTTAGTAGAGACGGGGTTTCA T A CPLX1 Ensembl:ENSG00000168993 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1183042877 Functional Loss SNV dbSNP153 33..33 33 - - - 20366 RMVar_ID_20366 Human_SNP_ID_170268914 A-to-I Human chr4 - 813178 813178 813178 TCACTGCAACCTCCGGCTCCCAGGTTCAAGCAATTCTCCTGCCTCACCCTCCCAAGTAGCTGGGA TCACTGCAACCTCCGGCTCCCAGGTTCAAGCAGTTCTCCTGCCTCACCCTCCCAAGTAGCTGGGA T C CPLX1 Ensembl:ENSG00000168993 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1435347132 Functional Loss SNV dbSNP153 33..33 33 - - - 20367 RMVar_ID_20367 Human_SNP_ID_170268915 A-to-I Human chr4 - 813179 813179 813179 CTCACTGCAACCTCCGGCTCCCAGGTTCAAGCAATTCTCCTGCCTCACCCTCCCAAGTAGCTGGG CTCACTGCAACCTCCGGCTCCCAGGTTCAAGCCATTCTCCTGCCTCACCCTCCCAAGTAGCTGGG T G CPLX1 Ensembl:ENSG00000168993 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1384782392 Functional Loss SNV dbSNP153 33..33 33 - - - 20368 RMVar_ID_20368 Human_SNP_ID_170298293 A-to-I Human chr4 - 897783 897783 897783 CACCACGCCCAGCTAATTTTTGTGTTTTTGGTAGGGACGGGGTTTCACCGTGTTGGCCAGGATGG CACCACGCCCAGCTAATTTTTGTGTTTTTGGTGGGGACGGGGTTTCACCGTGTTGGCCAGGATGG T C GAK Ensembl:ENSG00000178950 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1354447231 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21075598 RMVar_hsa_circ_63502,RMVar_hsa_circ_28170,RMVar_hsa_circ_364435,RMVar_hsa_circ_319770,RMVar_hsa_circ_224203,RMVar_hsa_circ_224205,RMVar_hsa_circ_319719,RMVar_hsa_circ_282375,RMVar_hsa_circ_224204,RMVar_hsa_circ_359816,RMVar_hsa_circ_297225,RMVar_hsa_circ_48399,RMVar_hsa_circ_290029,RMVar_hsa_circ_224206 20369 RMVar_ID_20369 Human_SNP_ID_170327985 A-to-I Human chr4 - 984574 984574 984574 CACCTGTCTCGGCCTCCCAAAGTGCTGGGATTATAGGCATGAGCCACCGCGCTGGGTCAAACTCC CACCTGTCTCGGCCTCCCAAAGTGCTGGGATTGTAGGCATGAGCCACCGCGCTGGGTCAAACTCC T C SLC26A1,DGKQ Ensembl:ENSG00000145217,Ensembl:ENSG00000145214 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1457080611 Functional Loss SNV dbSNP153 33..33 33 - - - 20370 RMVar_ID_20370 Human_SNP_ID_170336398 A-to-I Human chr4 + 1005867 1005867 1005867 ACACAGCCTCTGAGATGGAGTCTCGCTCTGTCACCCAGGCTGGAGTGCAGTGGCGTGATCTCGGC ACACAGCCTCTGAGATGGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCGTGATCTCGGC A G - - Other Unknown GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs939455565 Functional Loss SNV dbSNP153 33..33 33 - - - 20371 RMVar_ID_20371 Human_SNP_ID_170336399 A-to-I Human chr4 + 1005867 1005867 1005867 ACACAGCCTCTGAGATGGAGTCTCGCTCTGTCACCCAGGCTGGAGTGCAGTGGCGTGATCTCGGC ACACAGCCTCTGAGATGGAGTCTCGCTCTGTCTCCCAGGCTGGAGTGCAGTGGCGTGATCTCGGC A T - - Other Unknown GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs939455565 Functional Loss SNV dbSNP153 33..33 33 - - - 20372 RMVar_ID_20372 Human_SNP_ID_170363378 A-to-I Human chr4 - 1084513 1084513 1084513 GTTACCCAGGCTAGTCTTGGACTCCTGAGCTCAAGTGATCCTCCCACCTCAGCGTCCCAAAGTGC GTTACCCAGGCTAGTCTTGGACTCCTGAGCTCGAGTGATCCTCCCACCTCAGCGTCCCAAAGTGC T C RNF212 Ensembl:ENSG00000178222 Protein coding intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1361829595 Functional Loss SNV dbSNP153 33..33 33 - - - 20373 RMVar_ID_20373 Human_SNP_ID_170389460 A-to-I Human chr4 - 1173997 1173997 1173997 TGAGGTCTCCCTGTGTTGCCAAGGCTGGTATCAAACTCTGGGCTCAAGTGATCCTCCCGCCTCGG TGAGGTCTCCCTGTGTTGCCAAGGCTGGTATCGAACTCTGGGCTCAAGTGATCCTCCCGCCTCGG T C SPON2 Ensembl:ENSG00000159674 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1430278155 Functional Loss SNV dbSNP153 33..33 33 - - - 20374 RMVar_ID_20374 Human_SNP_ID_170389462 A-to-I Human chr4 - 1174000 1174000 1174000 AGATGAGGTCTCCCTGTGTTGCCAAGGCTGGTATCAAACTCTGGGCTCAAGTGATCCTCCCGCCT AGATGAGGTCTCCCTGTGTTGCCAAGGCTGGTCTCAAACTCTGGGCTCAAGTGATCCTCCCGCCT T G SPON2 Ensembl:ENSG00000159674 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1193803881 Functional Loss SNV dbSNP153 33..33 33 - - - 20375 RMVar_ID_20375 Human_SNP_ID_170391911 A-to-I Human chr4 - 1183158 1183158 1183158 TGCTGACTGCAACCTCCACCTCCCGTGTTCTAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAACT TGCTGACTGCAACCTCCACCTCCCGTGTTCTACGCGATTCTCCTGCCTCAGCCTCCTGAGTAACT T G SPON2 Ensembl:ENSG00000159674 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1178893508 Functional Loss SNV dbSNP153 33..33 33 - - - 20376 RMVar_ID_20376 Human_SNP_ID_170392266 A-to-I Human chr4 - 1184750 1184750 1184750 TAAATTTTTGTTTAGTAGAGACGGGTTTCACTATGTTGACCAGACTGGTCATGAACTCCTGACCT TAAATTTTTGTTTAGTAGAGACGGGTTTCACTGTGTTGACCAGACTGGTCATGAACTCCTGACCT T C SPON2 Ensembl:ENSG00000159674 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs868831434 Functional Loss SNV dbSNP153 33..33 33 - - - 20377 RMVar_ID_20377 Human_SNP_ID_170392267 A-to-I Human chr4 - 1184750 1184750 1184750 TAAATTTTTGTTTAGTAGAGACGGGTTTCACTATGTTGACCAGACTGGTCATGAACTCCTGACCT TAAATTTTTGTTTAGTAGAGACGGGTTTCACTCTGTTGACCAGACTGGTCATGAACTCCTGACCT T G SPON2 Ensembl:ENSG00000159674 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs868831434 Functional Loss SNV dbSNP153 33..33 33 - - - 20378 RMVar_ID_20378 Human_SNP_ID_170393018 A-to-I Human chr4 - 1186441 1186441 1186441 AAATTAGCCGGGCACGGCAGCATGCGCCTGCAATCCCAGCTACTTGGGAGGTTGAGACAGGAGAA AAATTAGCCGGGCACGGCAGCATGCGCCTGCACTCCCAGCTACTTGGGAGGTTGAGACAGGAGAA T G SPON2 Ensembl:ENSG00000159674 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs529153594 Functional Loss SNV dbSNP153 33..33 33 - - - 20379 RMVar_ID_20379 Human_SNP_ID_170418683 A-to-I Human chr4 + 1263974 1263974 1263974 TGCCTGCCTAATTTTTTAAAATTTATTTTTGTAGAGACAGACTGTCACTATGTTGCCTAGGCTGG TGCCTGCCTAATTTTTTAAAATTTATTTTTGTGGAGACAGACTGTCACTATGTTGCCTAGGCTGG A G CTBP1-DT Ensembl:ENSG00000196810 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1483784795 Functional Loss SNV dbSNP153 33..33 33 - - - 20380 RMVar_ID_20380 Human_SNP_ID_170442172 A-to-I Human chr4 + 1337629 1337629 1337629 TCCCACCTGCAACTGACTTCTTCCTGCCTGTGACAGACTCTGCCCCTGCCTGCGACTGAGTCTGT TCCCACCTGCAACTGACTTCTTCCTGCCTGTGGCAGACTCTGCCCCTGCCTGCGACTGAGTCTGT A G MAEA Ensembl:ENSG00000090316 Protein coding intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs557001777 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17089710,Human_RBP_ID_21081538 RMVar_hsa_circ_84625,RMVar_hsa_circ_224238 20381 RMVar_ID_20381 Human_SNP_ID_170446782 A-to-I Human chr4 + 1350691 1350691 1350691 AGGGTGCACACCCACAGTCCCACTGACTCTGGAAGCCGAGGCTGGTGGATCACCTGGTCCTGGGA AGGGTGCACACCCACAGTCCCACTGACTCTGGTAGCCGAGGCTGGTGGATCACCTGGTCCTGGGA A T UVSSA Ensembl:ENSG00000163945 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985407687 Functional Loss SNV dbSNP153 33..33 33 - - - 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_53920,RMVar_hsa_circ_316694,RMVar_hsa_circ_297754,RMVar_hsa_circ_297951,RMVar_hsa_circ_224244 20382 RMVar_ID_20382 Human_SNP_ID_170446787 A-to-I Human chr4 + 1350697 1350697 1350697 CACACCCACAGTCCCACTGACTCTGGAAGCCGAGGCTGGTGGATCACCTGGTCCTGGGAGTTTGA CACACCCACAGTCCCACTGACTCTGGAAGCCGGGGCTGGTGGATCACCTGGTCCTGGGAGTTTGA A G UVSSA Ensembl:ENSG00000163945 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1137636 Functional Loss SNV dbSNP153 33..33 33 - - - 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_53920,RMVar_hsa_circ_316694,RMVar_hsa_circ_297754,RMVar_hsa_circ_297951,RMVar_hsa_circ_224244 20383 RMVar_ID_20383 Human_SNP_ID_170459932 A-to-I Human chr4 + 1386792 1386792 1386792 CCAGGCTGAGTGCAGTGGCAGAATCATAGCTCAGTGCAGCCTCAAACTCCTGGGCTCAAGCCATC CCAGGCTGAGTGCAGTGGCAGAATCATAGCTCTGTGCAGCCTCAAACTCCTGGGCTCAAGCCATC A T UVSSA Ensembl:ENSG00000163945 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1214131504 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18818660 20384 RMVar_ID_20384 Human_SNP_ID_170460677 A-to-I Human chr4 + 1389451 1389451 1389451 TGGAGTACAGTAGCACAATCATGGCTCACTACAGCTTTGACCTCCCAGACTCAAGCAATCTTCCC TGGAGTACAGTAGCACAATCATGGCTCACTACGGCTTTGACCTCCCAGACTCAAGCAATCTTCCC A G UVSSA Ensembl:ENSG00000163945 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1305783455 Functional Loss SNV dbSNP153 33..33 33 - - - 20385 RMVar_ID_20385 Human_SNP_ID_170460678 A-to-I Human chr4 + 1389471 1389471 1389471 ATGGCTCACTACAGCTTTGACCTCCCAGACTCAAGCAATCTTCCCATCTCAGCTTCCTGAGTAGC ATGGCTCACTACAGCTTTGACCTCCCAGACTCGAGCAATCTTCCCATCTCAGCTTCCTGAGTAGC A G UVSSA Ensembl:ENSG00000163945 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1228525952 Functional Loss SNV dbSNP153 33..33 33 - - - 20386 RMVar_ID_20386 Human_SNP_ID_170461687 A-to-I Human chr4 + 1393455 1393455 1393455 TGTGCACCTGTAATCCCAGCTACTTGGGAGGCAGAGGCAGGAGAATTGCTTGAACCCGGGAGGCA TGTGCACCTGTAATCCCAGCTACTTGGGAGGCCGAGGCAGGAGAATTGCTTGAACCCGGGAGGCA A C UVSSA,AC118281.1 Ensembl:ENSG00000163945,Ensembl:ENSG00000288380 Protein coding,Protein coding 3'UTR,5'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs1228909121 Functional Loss SNV dbSNP153 33..33 33 - - - 20387 RMVar_ID_20387 Human_SNP_ID_170461689 A-to-I Human chr4 + 1393461 1393461 1393461 CCTGTAATCCCAGCTACTTGGGAGGCAGAGGCAGGAGAATTGCTTGAACCCGGGAGGCAGAGGTT CCTGTAATCCCAGCTACTTGGGAGGCAGAGGCGGGAGAATTGCTTGAACCCGGGAGGCAGAGGTT A G UVSSA,AC118281.1 Ensembl:ENSG00000163945,Ensembl:ENSG00000288380 Protein coding,Protein coding 3'UTR,5'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1052192764 Functional Loss SNV dbSNP153 33..33 33 - - - 20388 RMVar_ID_20388 Human_SNP_ID_170554584 A-to-I Human chr4 - 1695771 1695771 1695771 CTTTCTTTCTCTGTTGGCTTTTTTTTTTTGGGAGATGCTCTGTCACCGAGGCTGGAGTGCAGTGG CTTTCTTTCTCTGTTGGCTTTTTTTTTTTGGGGGATGCTCTGTCACCGAGGCTGGAGTGCAGTGG T C SLBP Ensembl:ENSG00000163950 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1208020773 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7285624,Human_RBP_ID_15090611 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_285512,RMVar_hsa_circ_224250,RMVar_hsa_circ_224251 20389 RMVar_ID_20389 Human_SNP_ID_170554585 A-to-I Human chr4 - 1695771 1695771 1695771 CTTTCTTTCTCTGTTGGCTTTTTTTTTTTGGGAGATGCTCTGTCACCGAGGCTGGAGTGCAGTGG CTTTCTTTCTCTGTTGGCTTTTTTTTTTTGGGCGATGCTCTGTCACCGAGGCTGGAGTGCAGTGG T G SLBP Ensembl:ENSG00000163950 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1208020773 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7285624,Human_RBP_ID_15090611 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_285512,RMVar_hsa_circ_224250,RMVar_hsa_circ_224251 20390 RMVar_ID_20390 Human_SNP_ID_170555233 A-to-I Human chr4 - 1697895 1697895 1697895 TCTTGAACTCCTGGCCTCAAGTAGTCCTCCCAAAGTACTGTGATTACAAGCGTGAGCCACTGTGC TCTTGAACTCCTGGCCTCAAGTAGTCCTCCCAGAGTACTGTGATTACAAGCGTGAGCCACTGTGC T C SLBP Ensembl:ENSG00000163950 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs750594919 Functional Loss SNV dbSNP153 33..33 33 - - - 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_326624 20391 RMVar_ID_20391 Human_SNP_ID_170555234 A-to-I Human chr4 - 1697895 1697895 1697895 TCTTGAACTCCTGGCCTCAAGTAGTCCTCCCAAAGTACTGTGATTACAAGCGTGAGCCACTGTGC TCTTGAACTCCTGGCCTCAAGTAGTCCTCCCACAGTACTGTGATTACAAGCGTGAGCCACTGTGC T G SLBP Ensembl:ENSG00000163950 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs750594919 Functional Loss SNV dbSNP153 33..33 33 - - - 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_326624 20392 RMVar_ID_20392 Human_SNP_ID_170555274 A-to-I Human chr4 - 1698040 1698040 1698040 CTCACTGTAGTCTTAACTCCTGGCCTCAAGCAATCCTCCTACCTCAACCTCCTGAGTAGCTGGGA CTCACTGTAGTCTTAACTCCTGGCCTCAAGCAGTCCTCCTACCTCAACCTCCTGAGTAGCTGGGA T C SLBP Ensembl:ENSG00000163950 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs527897364 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15237841 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_326624 20393 RMVar_ID_20393 Human_SNP_ID_170555317 A-to-I Human chr4 - 1698175 1698175 1698175 TCGTATTTTCAGTAGAGATGGGGTTTTACCATATTGGCCAGGCTGGTCTCGCACTGCTGATCTCG TCGTATTTTCAGTAGAGATGGGGTTTTACCATGTTGGCCAGGCTGGTCTCGCACTGCTGATCTCG T C SLBP Ensembl:ENSG00000163950 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs952305443 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15091498 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_326624 20394 RMVar_ID_20394 Human_SNP_ID_170555600 A-to-I Human chr4 - 1698961 1698961 1698961 ATATAAGGAGACCTCATCTCTACAAAAAATTTAAAAATTAGCCAGGTGTGGTGGTTTGCACCTGT ATATAAGGAGACCTCATCTCTACAAAAAATTTTAAAATTAGCCAGGTGTGGTGGTTTGCACCTGT T A SLBP Ensembl:ENSG00000163950 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1258002587 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15091747 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_326624 20395 RMVar_ID_20395 Human_SNP_ID_170555629 A-to-I Human chr4 - 1699067 1699067 1699067 GGGTTGAAATTTACATTTCTGGGCCAGGTGCAATGGCTCATGCTTGTAATTCCAGCACTTTGGGA GGGTTGAAATTTACATTTCTGGGCCAGGTGCAGTGGCTCATGCTTGTAATTCCAGCACTTTGGGA T C SLBP Ensembl:ENSG00000163950 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs950462343 Functional Loss SNV dbSNP153 33..33 33 - - - 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_326624 20396 RMVar_ID_20396 Human_SNP_ID_170556305 A-to-I Human chr4 - 1701274 1701274 1701274 AGGCGTGGTGGCAGCAACCTGTAATCTCAGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGGA AGGCGTGGTGGCAGCAACCTGTAATCTCAGCTTCTCAGGAGGCTGAGGCAGGAGAATCGCTTGGA T A SLBP Ensembl:ENSG00000163950 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1416417130 Functional Loss SNV dbSNP153 33..33 33 - - - 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_64168 20397 RMVar_ID_20397 Human_SNP_ID_170556325 A-to-I Human chr4 - 1701348 1701348 1701348 GAGATCAGGAGTTCGAGACCAGCCTGACGAACATGGAGAAACCCCGTCTCTACTAAAAATACTAA GAGATCAGGAGTTCGAGACCAGCCTGACGAACGTGGAGAAACCCCGTCTCTACTAAAAATACTAA T C SLBP Ensembl:ENSG00000163950 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1319222901 Functional Loss SNV dbSNP153 33..33 33 - - - 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_64168 20398 RMVar_ID_20398 Human_SNP_ID_170556426 A-to-I Human chr4 - 1701715 1701715 1701715 TTTAGTAGAGGCTAGGTTTCACCATATTGGCCAGGCTGGTCTTGAACTCCTGACCTCAGGTGATT TTTAGTAGAGGCTAGGTTTCACCATATTGGCCCGGCTGGTCTTGAACTCCTGACCTCAGGTGATT T G SLBP Ensembl:ENSG00000163950 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1348399685 Functional Loss SNV dbSNP153 33..33 33 - - - 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_64168 20399 RMVar_ID_20399 Human_SNP_ID_170556432 A-to-I Human chr4 - 1701744 1701744 1701744 TGCCACCACGTCCGGCTAATTTTTGTATTTTTAGTAGAGGCTAGGTTTCACCATATTGGCCAGGC TGCCACCACGTCCGGCTAATTTTTGTATTTTTGGTAGAGGCTAGGTTTCACCATATTGGCCAGGC T C SLBP Ensembl:ENSG00000163950 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1283448086 Functional Loss SNV dbSNP153 33..33 33 - - - 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_64168 20400 RMVar_ID_20400 Human_SNP_ID_170557355 A-to-I Human chr4 - 1705066 1705044 1705067 AAAATTAGCTGGACGTGGTGGCTCATGCCTGTAATTTCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTAGCTGGACGTGGTGGCTCATGCCTG_______________________GAGGCAGGAGA CAGCCTCCCGAGTAGCTGAAATTA C SLBP Ensembl:ENSG00000163950 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1466319793 Functional Loss DEL dbSNP153 32..54 33 - - - 20401 RMVar_ID_20401 Human_SNP_ID_170557364 A-to-I Human chr4 - 1705065 1705065 1705065 AAATTAGCTGGACGTGGTGGCTCATGCCTGTAATTTCAGCTACTCGGGAGGCTGAGGCAGGAGAA AAATTAGCTGGACGTGGTGGCTCATGCCTGTAGTTTCAGCTACTCGGGAGGCTGAGGCAGGAGAA T C SLBP Ensembl:ENSG00000163950 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1182826167 Functional Loss SNV dbSNP153 33..33 33 - - - 20402 RMVar_ID_20402 Human_SNP_ID_170557394 A-to-I Human chr4 - 1705173 1705173 1705173 GCTATAATCCCAGTACTTTGGGAGGCCGAGGCAGGTGGATCACCTGAGGTCAGGAGTTCGAGACC GCTATAATCCCAGTACTTTGGGAGGCCGAGGCGGGTGGATCACCTGAGGTCAGGAGTTCGAGACC T C SLBP Ensembl:ENSG00000163950 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1323339669 Functional Loss SNV dbSNP153 33..33 33 - - - 20403 RMVar_ID_20403 Human_SNP_ID_170557401 A-to-I Human chr4 - 1705202 1705202 1705202 TCAGTGCAGTCTGGGTACGGTGGCTCACAGCTATAATCCCAGTACTTTGGGAGGCCGAGGCAGGT TCAGTGCAGTCTGGGTACGGTGGCTCACAGCTGTAATCCCAGTACTTTGGGAGGCCGAGGCAGGT T C SLBP Ensembl:ENSG00000163950 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs901625728 Functional Loss SNV dbSNP153 33..33 33 - - - 20404 RMVar_ID_20404 Human_SNP_ID_170558625 A-to-I Human chr4 - 1709192 1709192 1709192 GGGCATGGTGGCGCATGCCTGTAATCCCAGCTACTCGGGAGGTTGAGGCAGGAGAATCCCTTGAA GGGCATGGTGGCGCATGCCTGTAATCCCAGCTTCTCGGGAGGTTGAGGCAGGAGAATCCCTTGAA T A SLBP Ensembl:ENSG00000163950 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1360693136 Functional Loss SNV dbSNP153 33..33 33 - - - 20405 RMVar_ID_20405 Human_SNP_ID_170559224 A-to-I Human chr4 - 1710820 1710820 1710820 GTGTCGAACTCCTGACCTCAAGTGATCCACCCACCTTGGCCACCCAAAGTGCTGGGATTACAGGT GTGTCGAACTCCTGACCTCAAGTGATCCACCCGCCTTGGCCACCCAAAGTGCTGGGATTACAGGT T C SLBP Ensembl:ENSG00000163950 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs371399499 Functional Loss SNV dbSNP153 33..33 33 - - - 20406 RMVar_ID_20406 Human_SNP_ID_170566740 A-to-I Human chr4 + 1731895 1731895 1731895 ACCTCAAGTGATCCACCTGCCTCGGCCTCCCAAAGTGCTGGGATTGCACGCGTGAGCCCCCGCGC ACCTCAAGTGATCCACCTGCCTCGGCCTCCCACAGTGCTGGGATTGCACGCGTGAGCCCCCGCGC A C TACC3 Ensembl:ENSG00000013810 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs774872402 Functional Loss SNV dbSNP153 33..33 33 - - - 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 20407 RMVar_ID_20407 Human_SNP_ID_170566741 A-to-I Human chr4 + 1731895 1731895 1731895 ACCTCAAGTGATCCACCTGCCTCGGCCTCCCAAAGTGCTGGGATTGCACGCGTGAGCCCCCGCGC ACCTCAAGTGATCCACCTGCCTCGGCCTCCCAGAGTGCTGGGATTGCACGCGTGAGCCCCCGCGC A G TACC3 Ensembl:ENSG00000013810 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs774872402 Functional Loss SNV dbSNP153 33..33 33 - - - 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 20408 RMVar_ID_20408 Human_SNP_ID_170603977 A-to-I Human chr4 - 1838522 1838522 1838522 CAGACGCACGCTGTCATGCCAGGCTAATTTTTAAATTTTTCGTAGAGACTGGGTCTCACTATATT CAGACGCACGCTGTCATGCCAGGCTAATTTTTTAATTTTTCGTAGAGACTGGGTCTCACTATATT T A LETM1 Ensembl:ENSG00000168924 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1354017280 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111913,RMVar_hsa_circ_224284,RMVar_hsa_circ_7316,RMVar_hsa_circ_51890,RMVar_hsa_circ_224287,RMVar_hsa_circ_289544,RMVar_hsa_circ_101495,RMVar_hsa_circ_348236 20409 RMVar_ID_20409 Human_SNP_ID_170610119 A-to-I Human chr4 + 1860053 1860053 1860053 CCAGCTGCTTGACAGGCTGAGGCAGGAGAATCACTTGAACCCTGGAGATGGACGTTGCAGTGAGC CCAGCTGCTTGACAGGCTGAGGCAGGAGAATCCCTTGAACCCTGGAGATGGACGTTGCAGTGAGC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1364505246 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15111875 20410 RMVar_ID_20410 Human_SNP_ID_170610580 A-to-I Human chr4 + 1860894 1860894 1860894 TGTATTTTTTTGTAGAGATGGGGTCTCGCCACATTGTCCAGGCTGGTCTTGAACTCTTGGGCTCA TGTATTTTTTTGTAGAGATGGGGTCTCGCCACGTTGTCCAGGCTGGTCTTGAACTCTTGGGCTCA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053978706 Functional Loss SNV dbSNP153 33..33 33 - - - 20411 RMVar_ID_20411 Human_SNP_ID_170615165 A-to-I Human chr4 + 1875031 1875031 1875031 TTACCTGGTGTGGAGTGCAGTGGTTCAATCATAGCTCACTGTAACCTGGCACTCCTGGGCTCAAG TTACCTGGTGTGGAGTGCAGTGGTTCAATCATGGCTCACTGTAACCTGGCACTCCTGGGCTCAAG A G NSD2 Ensembl:ENSG00000109685 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs954557603 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8588710,Human_RBP_ID_15113991 20412 RMVar_ID_20412 Human_SNP_ID_170615279 A-to-I Human chr4 + 1875394 1875394 1875394 GCCTTGATCACCTGGGCTCAATCGATCCTCCTACCTCAGCCTCCTGAGTAGCTGGGACAACAGGC GCCTTGATCACCTGGGCTCAATCGATCCTCCTGCCTCAGCCTCCTGAGTAGCTGGGACAACAGGC A G NSD2 Ensembl:ENSG00000109685 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1013260483 Functional Loss SNV dbSNP153 33..33 33 - - - 20413 RMVar_ID_20413 Human_SNP_ID_170615621 A-to-I Human chr4 + 1876569 1876569 1876569 TGAAAATTAGCTGGGCTTGGTGGTGTGTGCCTATAGTCCCAGATACTTGGGTGGCTGAAGTGGGA TGAAAATTAGCTGGGCTTGGTGGTGTGTGCCTGTAGTCCCAGATACTTGGGTGGCTGAAGTGGGA A G NSD2 Ensembl:ENSG00000109685 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs767802642 Functional Loss SNV dbSNP153 33..33 33 - - - 20414 RMVar_ID_20414 Human_SNP_ID_170617133 A-to-I Human chr4 + 1881597 1881597 1881597 TTTTTGTTTTTAAATAGAGACAGGGTTTTGCCATGTTGCCCAGGCTGGTCTTGAATTCCTCGACT TTTTTGTTTTTAAATAGAGACAGGGTTTTGCCCTGTTGCCCAGGCTGGTCTTGAATTCCTCGACT A C NSD2 Ensembl:ENSG00000109685 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs911557167 Functional Loss SNV dbSNP153 33..33 33 - - - 20415 RMVar_ID_20415 Human_SNP_ID_170617134 A-to-I Human chr4 + 1881597 1881597 1881597 TTTTTGTTTTTAAATAGAGACAGGGTTTTGCCATGTTGCCCAGGCTGGTCTTGAATTCCTCGACT TTTTTGTTTTTAAATAGAGACAGGGTTTTGCCGTGTTGCCCAGGCTGGTCTTGAATTCCTCGACT A G NSD2 Ensembl:ENSG00000109685 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs911557167 Functional Loss SNV dbSNP153 33..33 33 - - - 20416 RMVar_ID_20416 Human_SNP_ID_170617346 A-to-I Human chr4 + 1882409 1882409 1882409 ACTTTGGGCTGGGCTTAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGTGG ACTTTGGGCTGGGCTTAGTGGCTCATGCCTGTGATCCCAGCACTTTGGGAGGCCGAGGCGGGTGG A G NSD2 Ensembl:ENSG00000109685 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs961885620 Functional Loss SNV dbSNP153 33..33 33 - - - 20417 RMVar_ID_20417 Human_SNP_ID_170617879 A-to-I Human chr4 + 1884221 1884221 1884221 GGGTTCAAGCCATCCTCCCACCTCAGCCTCCCAAGTAGCTGGGACTATGGGTGCATGCTACTGTG GGGTTCAAGCCATCCTCCCACCTCAGCCTCCCGAGTAGCTGGGACTATGGGTGCATGCTACTGTG A G NSD2 Ensembl:ENSG00000109685 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1178732301 Functional Loss SNV dbSNP153 33..33 33 - - - 20418 RMVar_ID_20418 Human_SNP_ID_170618450 A-to-I Human chr4 + 1886324 1886324 1886324 CATCTCCTGGGCTCAGGCAATTCTCGTGCCTCAGTCTCCTGAATAGCTGGTATTACAGGTGTGCA CATCTCCTGGGCTCAGGCAATTCTCGTGCCTCGGTCTCCTGAATAGCTGGTATTACAGGTGTGCA A G NSD2 Ensembl:ENSG00000109685 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1396965968 Functional Loss SNV dbSNP153 33..33 33 - - - 20419 RMVar_ID_20419 Human_SNP_ID_170618476 A-to-I Human chr4 + 1886468 1886468 1886468 GCCTCAAGTGATTCACTCATCTTGGCCTCTGAAAGTTCTGGGATTACGGACTTGAGCCACTGTGC GCCTCAAGTGATTCACTCATCTTGGCCTCTGACAGTTCTGGGATTACGGACTTGAGCCACTGTGC A C NSD2 Ensembl:ENSG00000109685 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251544109 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15114518,Human_RBP_ID_17574692 20420 RMVar_ID_20420 Human_SNP_ID_170618577 A-to-I Human chr4 + 1886717 1886717 1886717 AAAATTAGCCAGGCGTGGTGGCGTGCACCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGGTA AAAATTAGCCAGGCGTGGTGGCGTGCACCTGTGGTCCCAGCTACTCAGGAGGCTGAGGCAGGGTA A G NSD2 Ensembl:ENSG00000109685 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs374426276 Functional Loss SNV dbSNP153 33..33 33 - - - 20421 RMVar_ID_20421 Human_SNP_ID_170618581 A-to-I Human chr4 + 1886727 1886726 1886728 AGGCGTGGTGGCGTGCACCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGGTACTCGCTTGAA AGGCGTGGTGGCGTGCACCTGTAGTCCCAGCT__TCAGGAGGCTGAGGCAGGGTACTCGCTTGAA TAC T NSD2 Ensembl:ENSG00000109685 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1457024516 Functional Loss DEL dbSNP153 33..34 33 - - - 20422 RMVar_ID_20422 Human_SNP_ID_170618594 A-to-I Human chr4 + 1886758 1886758 1886758 TACTCAGGAGGCTGAGGCAGGGTACTCGCTTGAACCTGGGGAGGTGGAGGTTGCAGTGAGCTGAG TACTCAGGAGGCTGAGGCAGGGTACTCGCTTGTACCTGGGGAGGTGGAGGTTGCAGTGAGCTGAG A T NSD2 Ensembl:ENSG00000109685 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1281170546 Functional Loss SNV dbSNP153 33..33 33 - - - 20423 RMVar_ID_20423 Human_SNP_ID_170619387 A-to-I Human chr4 + 1889601 1889601 1889601 TCGGCTTACTGTAACCTCCGCCTCCTGAGTTCAAGCGATTCTCCTTCCTCAGCCTCCCAGGTAAC TCGGCTTACTGTAACCTCCGCCTCCTGAGTTCCAGCGATTCTCCTTCCTCAGCCTCCCAGGTAAC A C NSD2 Ensembl:ENSG00000109685 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1437319633 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15114671 20424 RMVar_ID_20424 Human_SNP_ID_170619406 A-to-I Human chr4 + 1889681 1889681 1889681 GTGCTACCATGCCTGGCTAATTTTGTATTTTTAGTAGAGAGAGTTTCATCATGTTGGTCAGGCTG GTGCTACCATGCCTGGCTAATTTTGTATTTTTGGTAGAGAGAGTTTCATCATGTTGGTCAGGCTG A G NSD2 Ensembl:ENSG00000109685 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs572806303 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15114672,Human_RBP_ID_23313252 20425 RMVar_ID_20425 Human_SNP_ID_170620074 A-to-I Human chr4 + 1891736 1891736 1891736 AAAATTAGCCGGGCGTGGTGGTCGGCACCTGTAGTTCCAGCTACTCGGCAGGCTGAGGCAGGAGA AAAATTAGCCGGGCGTGGTGGTCGGCACCTGTGGTTCCAGCTACTCGGCAGGCTGAGGCAGGAGA A G NSD2 Ensembl:ENSG00000109685 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1393047507 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23313255 20426 RMVar_ID_20426 Human_SNP_ID_170620238 A-to-I Human chr4 + 1892186 1892186 1892186 TTTTAATTTTAGAGATGGGTCTCGCCATCACCATGTTGCCCAGTCTGGTCTCCAACTCCTGGGCT TTTTAATTTTAGAGATGGGTCTCGCCATCACCGTGTTGCCCAGTCTGGTCTCCAACTCCTGGGCT A G NSD2 Ensembl:ENSG00000109685 Protein coding intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1365084731 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_538308,Human_Splice_Rec_538309 RMVar_hsa_circ_224288,RMVar_hsa_circ_309146 20427 RMVar_ID_20427 Human_SNP_ID_170620246 A-to-I Human chr4 + 1892220 1892220 1892220 GTTGCCCAGTCTGGTCTCCAACTCCTGGGCTCAAGCGATCCTCCTGCCTTGGTCTCCCAAAGTGC GTTGCCCAGTCTGGTCTCCAACTCCTGGGCTCCAGCGATCCTCCTGCCTTGGTCTCCCAAAGTGC A C NSD2 Ensembl:ENSG00000109685 Protein coding intron GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs1470548766 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_538308,Human_Splice_Rec_538309 RMVar_hsa_circ_224288,RMVar_hsa_circ_309146 20428 RMVar_ID_20428 Human_SNP_ID_170620391 A-to-I Human chr4 + 1892698 1892698 1892698 TTGAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTATAGGCGTGCACCACCACGCCTG TTGAGCGATTCTCCTGCCTCAGCCTCCTGAGTCGCTGGGATTATAGGCGTGCACCACCACGCCTG A C NSD2 Ensembl:ENSG00000109685 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs972944349 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_224288,RMVar_hsa_circ_309146 20429 RMVar_ID_20429 Human_SNP_ID_170620829 A-to-I Human chr4 + 1894140 1894139 1894140 CACTGTACCTGGCTAAATTTAAAATTTTTTGTAGAGACGGCGTCTTACTATGTTGGCCAGGCTGG CACTGTACCTGGCTAAATTTAAAATTTTTTGT_GAGACGGCGTCTTACTATGTTGGCCAGGCTGG TA T NSD2 Ensembl:ENSG00000109685 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1176289304 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_224288,RMVar_hsa_circ_115170,RMVar_hsa_circ_224291,RMVar_hsa_circ_224290,RMVar_hsa_circ_79323 20430 RMVar_ID_20430 Human_SNP_ID_170621497 A-to-I Human chr4 + 1896555 1896554 1896556 TGTGCCTGGCTAATTTTATTTTTTGTAGAGACAGGGTCTCACTATGCTGCCCAGGCTCATCTCAA TGTGCCTGGCTAATTTTATTTTTTGTAGAGAC__GGTCTCACTATGCTGCCCAGGCTCATCTCAA CAG C NSD2 Ensembl:ENSG00000109685 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1438736097 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_224288,RMVar_hsa_circ_115170,RMVar_hsa_circ_224291,RMVar_hsa_circ_224290,RMVar_hsa_circ_79323 20431 RMVar_ID_20431 Human_SNP_ID_170621498 A-to-I Human chr4 + 1896555 1896555 1896555 TGTGCCTGGCTAATTTTATTTTTTGTAGAGACAGGGTCTCACTATGCTGCCCAGGCTCATCTCAA TGTGCCTGGCTAATTTTATTTTTTGTAGAGACGGGGTCTCACTATGCTGCCCAGGCTCATCTCAA A G NSD2 Ensembl:ENSG00000109685 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1023993792 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_224288,RMVar_hsa_circ_115170,RMVar_hsa_circ_224291,RMVar_hsa_circ_224290,RMVar_hsa_circ_79323 20432 RMVar_ID_20432 Human_SNP_ID_170621657 A-to-I Human chr4 + 1896937 1896937 1896937 TCACATCTGTAATCCCAGCACTTTGAAAGGCCAAGGCGGGTGGATCGCTTGAGCCCAGGAGTTGG TCACATCTGTAATCCCAGCACTTTGAAAGGCCGAGGCGGGTGGATCGCTTGAGCCCAGGAGTTGG A G NSD2 Ensembl:ENSG00000109685 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1438369683 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17574695,Human_RBP_ID_21082515 RMVar_hsa_circ_224288,RMVar_hsa_circ_115170,RMVar_hsa_circ_224291,RMVar_hsa_circ_224290,RMVar_hsa_circ_79323 20433 RMVar_ID_20433 Human_SNP_ID_170621747 A-to-I Human chr4 + 1897300 1897300 1897300 GCCCAGGAGTTTGAGATCAGCCTGGACAATATAGTGAGATCCATCTCTACAAAAAAAGGGTTAAA GCCCAGGAGTTTGAGATCAGCCTGGACAATATCGTGAGATCCATCTCTACAAAAAAAGGGTTAAA A C NSD2 Ensembl:ENSG00000109685 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs548894132 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_224288,RMVar_hsa_circ_115170,RMVar_hsa_circ_224291,RMVar_hsa_circ_224290,RMVar_hsa_circ_79323 20434 RMVar_ID_20434 Human_SNP_ID_170621771 A-to-I Human chr4 + 1897362 1897362 1897362 AAAAAGTTAGCTGAGCATGGTGGGGTGCACCTATAGTCCCAGCTACTCGGGAGGCTGAGATGGGA AAAAAGTTAGCTGAGCATGGTGGGGTGCACCTGTAGTCCCAGCTACTCGGGAGGCTGAGATGGGA A G NSD2 Ensembl:ENSG00000109685 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1180735016 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17574696,Human_RBP_ID_23313580,Human_RBP_ID_25796450 RMVar_hsa_circ_224288,RMVar_hsa_circ_115170,RMVar_hsa_circ_224291,RMVar_hsa_circ_224290,RMVar_hsa_circ_79323 20435 RMVar_ID_20435 Human_SNP_ID_170621872 A-to-I Human chr4 + 1897726 1897726 1897726 TTTGCTTATTGCAGCCTCCACCTCCTGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGC TTTGCTTATTGCAGCCTCCACCTCCTGGGTTCGAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGC A G NSD2 Ensembl:ENSG00000109685 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1024998419 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_224288,RMVar_hsa_circ_115170,RMVar_hsa_circ_224291,RMVar_hsa_circ_224290,RMVar_hsa_circ_79323 20436 RMVar_ID_20436 Human_SNP_ID_170622138 A-to-I Human chr4 + 1898543 1898543 1898543 AAAATTAGCCGGGCGTGGTGGTGGGCGCCTGTAGTCCCAGCTACTCAGGAGGGTGAGGCAGGAGA AAAATTAGCCGGGCGTGGTGGTGGGCGCCTGTGGTCCCAGCTACTCAGGAGGGTGAGGCAGGAGA A G NSD2 Ensembl:ENSG00000109685 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs564936307 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_224288,RMVar_hsa_circ_115170,RMVar_hsa_circ_224291,RMVar_hsa_circ_224290,RMVar_hsa_circ_79323 20437 RMVar_ID_20437 Human_SNP_ID_170622140 A-to-I Human chr4 + 1898549 1898549 1898549 AGCCGGGCGTGGTGGTGGGCGCCTGTAGTCCCAGCTACTCAGGAGGGTGAGGCAGGAGAATTGAA AGCCGGGCGTGGTGGTGGGCGCCTGTAGTCCCGGCTACTCAGGAGGGTGAGGCAGGAGAATTGAA A G NSD2 Ensembl:ENSG00000109685 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1465863287 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_224288,RMVar_hsa_circ_115170,RMVar_hsa_circ_224291,RMVar_hsa_circ_224290,RMVar_hsa_circ_79323 20438 RMVar_ID_20438 Human_SNP_ID_170623382 A-to-I Human chr4 + 1902973 1902973 1902973 GAGGCAGGAAGATTGCTTGAGCCCAGGAGTTCAAGACTAGCCTGGGCAACATAGCGAGACCCGGT GAGGCAGGAAGATTGCTTGAGCCCAGGAGTTCGAGACTAGCCTGGGCAACATAGCGAGACCCGGT A G NSD2 Ensembl:ENSG00000109685 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs550146891 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_224288,RMVar_hsa_circ_115170,RMVar_hsa_circ_17687,RMVar_hsa_circ_275779,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_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_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 20439 RMVar_ID_20439 Human_SNP_ID_170631258 A-to-I Human chr4 - 1930887 1930887 1930887 CCACACGCACTTGGACCGCTGGCCCAAACCCCACGGGTCAGAAACAGGGAGAGTGGACACACTTC CCACACGCACTTGGACCGCTGGCCCAAACCCCGCGGGTCAGAAACAGGGAGAGTGGACACACTTC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs368834275 Functional Loss SNV dbSNP153 33..33 33 - - - 20440 RMVar_ID_20440 Human_SNP_ID_170632282 A-to-I Human chr4 + 1934456 1934456 1934456 CAGAGGTTGCAGTGAGCTGAGATTGTGCCATTACACTCCAGCCTGAGCTACAAGAGCGAAACTCC CAGAGGTTGCAGTGAGCTGAGATTGTGCCATTGCACTCCAGCCTGAGCTACAAGAGCGAAACTCC A G NSD2 Ensembl:ENSG00000109685 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1414621342 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_224288,RMVar_hsa_circ_17687,RMVar_hsa_circ_305754,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_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_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_368346,RMVar_hsa_circ_40720,RMVar_hsa_circ_224313,RMVar_hsa_circ_311800,RMVar_hsa_circ_321441,RMVar_hsa_circ_330618,RMVar_hsa_circ_50696,RMVar_hsa_circ_224314 20441 RMVar_ID_20441 Human_SNP_ID_170632793 A-to-I Human chr4 + 1935793 1935793 1935793 TGAGGCAGGAGAATTGCTTGAACCTGACAGGCAGAGGTTGCTGTGAGCTGAGATCATGCCACTGC TGAGGCAGGAGAATTGCTTGAACCTGACAGGCGGAGGTTGCTGTGAGCTGAGATCATGCCACTGC A G NSD2 Ensembl:ENSG00000109685 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs954287252 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1637173,Human_RBP_ID_8588871,Human_RBP_ID_15115923 RMVar_hsa_circ_224288,RMVar_hsa_circ_17687,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_289851,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_224298,RMVar_hsa_circ_224299,RMVar_hsa_circ_224297,RMVar_hsa_circ_267503,RMVar_hsa_circ_224294,RMVar_hsa_circ_224295,RMVar_hsa_circ_368346,RMVar_hsa_circ_40720,RMVar_hsa_circ_311800,RMVar_hsa_circ_321441,RMVar_hsa_circ_50696,RMVar_hsa_circ_35994,RMVar_hsa_circ_360820,RMVar_hsa_circ_224314,RMVar_hsa_circ_38892 20442 RMVar_ID_20442 Human_SNP_ID_170649907 A-to-I Human chr4 - 1993912 1993912 1993912 CCTGGATTCCCAGCACTGTGGGAGCATGAGGCAGGAGAATCGCTGGACCTGGGAAGGCGGAGGTT CCTGGATTCCCAGCACTGTGGGAGCATGAGGCGGGAGAATCGCTGGACCTGGGAAGGCGGAGGTT T C NELFA Ensembl:ENSG00000185049 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1344648178 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15117695 20443 RMVar_ID_20443 Human_SNP_ID_170652618 A-to-I Human chr4 - 2003988 2003988 2003988 TGCCCAGCTAATTAGCTAATTTTTGTATTTTTAGTGGAGACGGGGTTTCACCGTGTTGGCCAGGA TGCCCAGCTAATTAGCTAATTTTTGTATTTTTGGTGGAGACGGGGTTTCACCGTGTTGGCCAGGA T C NELFA Ensembl:ENSG00000185049 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992862049 Functional Loss SNV dbSNP153 33..33 33 - - - 20444 RMVar_ID_20444 Human_SNP_ID_170685541 A-to-I Human chr4 - 2120617 2120617 2120617 TAGTGATGAGCGCCTGTAATCCCAATTATTCGAGAGACTGAGACAGGAGAATCACTTGAACCCGG TAGTGATGAGCGCCTGTAATCCCAATTATTCGGGAGACTGAGACAGGAGAATCACTTGAACCCGG T C HAUS3,POLN Ensembl:ENSG00000214367,Ensembl:ENSG00000130997 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1248103406 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1248,RMVar_hsa_circ_50641,RMVar_hsa_circ_124613,RMVar_hsa_circ_224326,RMVar_hsa_circ_357598,RMVar_hsa_circ_59494,RMVar_hsa_circ_378136,RMVar_hsa_circ_88818,RMVar_hsa_circ_224327 20445 RMVar_ID_20445 Human_SNP_ID_170686579 A-to-I Human chr4 - 2124405 2124405 2124405 TAGCCGGATGAGGTGGCACACGCCTATCCTGTAGTCCTGGCTGCTTGGGAGGCTAAGGAGAGAGG TAGCCGGATGAGGTGGCACACGCCTATCCTGTGGTCCTGGCTGCTTGGGAGGCTAAGGAGAGAGG T C HAUS3,POLN Ensembl:ENSG00000214367,Ensembl:ENSG00000130997 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs972834440 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1248,RMVar_hsa_circ_50641,RMVar_hsa_circ_124613,RMVar_hsa_circ_224326,RMVar_hsa_circ_357598,RMVar_hsa_circ_59494,RMVar_hsa_circ_378136,RMVar_hsa_circ_88818,RMVar_hsa_circ_224327 20446 RMVar_ID_20446 Human_SNP_ID_170713267 A-to-I Human chr4 - 2228603 2228602 2228603 GGCCGGGTGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGTCGGCGATCATGA GGCCGGGTGCGGTGGCTCACGCCTGTAATCCC_GCACTTTGGGAGGCCGAGGTCGGCGATCATGA CT C HAUS3,POLN Ensembl:ENSG00000214367,Ensembl:ENSG00000130997 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1182188596 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_50641,RMVar_hsa_circ_357598,RMVar_hsa_circ_299991,RMVar_hsa_circ_15100,RMVar_hsa_circ_325866,RMVar_hsa_circ_98231,RMVar_hsa_circ_224332,RMVar_hsa_circ_224335,RMVar_hsa_circ_54291,RMVar_hsa_circ_327467,RMVar_hsa_circ_224340,RMVar_hsa_circ_27249,RMVar_hsa_circ_15244,RMVar_hsa_circ_271235,RMVar_hsa_circ_290056,RMVar_hsa_circ_301384,RMVar_hsa_circ_224343,RMVar_hsa_circ_224345,RMVar_hsa_circ_345102,RMVar_hsa_circ_72685 20447 RMVar_ID_20447 Human_SNP_ID_170713268 A-to-I Human chr4 - 2228617 2228602 2228618 AGTAAAAGCAGTGGGGCCGGGTGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAG AGTAAAAGCAGTGGGGCCGGGTGCGGTGGCT________________GCACTTTGGGAGGCCGAG CTGGGATTACAGGCGTG C HAUS3,POLN Ensembl:ENSG00000214367,Ensembl:ENSG00000130997 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1247871219 Functional Loss DEL dbSNP153 32..47 33 - - - Human_RBP_ID_25803317 RMVar_hsa_circ_50641,RMVar_hsa_circ_357598,RMVar_hsa_circ_299991,RMVar_hsa_circ_15100,RMVar_hsa_circ_325866,RMVar_hsa_circ_98231,RMVar_hsa_circ_224332,RMVar_hsa_circ_224335,RMVar_hsa_circ_54291,RMVar_hsa_circ_327467,RMVar_hsa_circ_224340,RMVar_hsa_circ_27249,RMVar_hsa_circ_15244,RMVar_hsa_circ_271235,RMVar_hsa_circ_290056,RMVar_hsa_circ_301384,RMVar_hsa_circ_224343,RMVar_hsa_circ_224345,RMVar_hsa_circ_345102,RMVar_hsa_circ_72685 20448 RMVar_ID_20448 Human_SNP_ID_170713269 A-to-I Human chr4 - 2228603 2228603 2228603 GGCCGGGTGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGTCGGCGATCATGA GGCCGGGTGCGGTGGCTCACGCCTGTAATCCCTGCACTTTGGGAGGCCGAGGTCGGCGATCATGA T A HAUS3,POLN Ensembl:ENSG00000214367,Ensembl:ENSG00000130997 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs367944896 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50641,RMVar_hsa_circ_357598,RMVar_hsa_circ_299991,RMVar_hsa_circ_15100,RMVar_hsa_circ_325866,RMVar_hsa_circ_98231,RMVar_hsa_circ_224332,RMVar_hsa_circ_224335,RMVar_hsa_circ_54291,RMVar_hsa_circ_327467,RMVar_hsa_circ_224340,RMVar_hsa_circ_27249,RMVar_hsa_circ_15244,RMVar_hsa_circ_271235,RMVar_hsa_circ_290056,RMVar_hsa_circ_301384,RMVar_hsa_circ_224343,RMVar_hsa_circ_224345,RMVar_hsa_circ_345102,RMVar_hsa_circ_72685 20449 RMVar_ID_20449 Human_SNP_ID_170713272 A-to-I Human chr4 - 2228608 2228607 2228608 AGTGGGGCCGGGTGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGTCGGCGAT AGTGGGGCCGGGTGCGGTGGCTCACGCCTGTA_TCCCAGCACTTTGGGAGGCCGAGGTCGGCGAT AT A HAUS3,POLN Ensembl:ENSG00000214367,Ensembl:ENSG00000130997 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1296777919 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_50641,RMVar_hsa_circ_357598,RMVar_hsa_circ_299991,RMVar_hsa_circ_15100,RMVar_hsa_circ_325866,RMVar_hsa_circ_98231,RMVar_hsa_circ_224332,RMVar_hsa_circ_224335,RMVar_hsa_circ_54291,RMVar_hsa_circ_327467,RMVar_hsa_circ_224340,RMVar_hsa_circ_27249,RMVar_hsa_circ_15244,RMVar_hsa_circ_271235,RMVar_hsa_circ_290056,RMVar_hsa_circ_301384,RMVar_hsa_circ_224343,RMVar_hsa_circ_224345,RMVar_hsa_circ_345102,RMVar_hsa_circ_72685 20450 RMVar_ID_20450 Human_SNP_ID_170713973 A-to-I Human chr4 - 2231338 2231338 2231338 TCCCGGCCTCCCAAAGTGCCGGAATTACAGGCATGAGCCACCACGCTCAGCCGCTATTAAATATT TCCCGGCCTCCCAAAGTGCCGGAATTACAGGCGTGAGCCACCACGCTCAGCCGCTATTAAATATT T C HAUS3,POLN Ensembl:ENSG00000214367,Ensembl:ENSG00000130997 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1418599055 Functional Loss SNV dbSNP153 33..33 33 - - - 20451 RMVar_ID_20451 Human_SNP_ID_170713976 A-to-I Human chr4 - 2231344 2231344 2231344 CCCCTCTCCCGGCCTCCCAAAGTGCCGGAATTACAGGCATGAGCCACCACGCTCAGCCGCTATTA CCCCTCTCCCGGCCTCCCAAAGTGCCGGAATTGCAGGCATGAGCCACCACGCTCAGCCGCTATTA T C HAUS3,POLN Ensembl:ENSG00000214367,Ensembl:ENSG00000130997 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984847368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_618816 20452 RMVar_ID_20452 Human_SNP_ID_170714043 A-to-I Human chr4 - 2231592 2231592 2231592 AAATTTTCTGCCGTTAAATTTTTTTTTGAGATAGAGTCTCACTCTGTCTCCAGGCTGGAATGCAG AAATTTTCTGCCGTTAAATTTTTTTTTGAGATGGAGTCTCACTCTGTCTCCAGGCTGGAATGCAG T C HAUS3,POLN Ensembl:ENSG00000214367,Ensembl:ENSG00000130997 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1033296125 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_618817,Human_RBP_ID_15126353,Human_RBP_ID_17523696 20453 RMVar_ID_20453 Human_SNP_ID_170738966 A-to-I Human chr4 - 2310722 2310722 2310722 TAGACTCACTGCAATCTCTGCCTCCCAGGCTCAAGCGATCCTCCCACCTCAGCCTCCTGAGTAGC TAGACTCACTGCAATCTCTGCCTCCCAGGCTCGAGCGATCCTCCCACCTCAGCCTCCTGAGTAGC T C ZFYVE28 Ensembl:ENSG00000159733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs557026920 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106010,RMVar_hsa_circ_83131,RMVar_hsa_circ_224350,RMVar_hsa_circ_224351 20454 RMVar_ID_20454 Human_SNP_ID_170738967 A-to-I Human chr4 - 2310728 2310728 2310728 ACAATCTAGACTCACTGCAATCTCTGCCTCCCAGGCTCAAGCGATCCTCCCACCTCAGCCTCCTG ACAATCTAGACTCACTGCAATCTCTGCCTCCCTGGCTCAAGCGATCCTCCCACCTCAGCCTCCTG T A ZFYVE28 Ensembl:ENSG00000159733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1418635321 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106010,RMVar_hsa_circ_83131,RMVar_hsa_circ_224350,RMVar_hsa_circ_224351 20455 RMVar_ID_20455 Human_SNP_ID_170739739 A-to-I Human chr4 - 2313674 2313674 2313674 TTCAGTACAGACTGGGTTTCACCATTTTGGCCAGGCTGGTCCTGAACTCCTGACCTCAAATGATC TTCAGTACAGACTGGGTTTCACCATTTTGGCCGGGCTGGTCCTGAACTCCTGACCTCAAATGATC T C ZFYVE28 Ensembl:ENSG00000159733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1011992227 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106010,RMVar_hsa_circ_83131,RMVar_hsa_circ_224350,RMVar_hsa_circ_224351 20456 RMVar_ID_20456 Human_SNP_ID_170750567 A-to-I Human chr4 - 2351095 2351095 2351095 CAAGACGGCCCCCCATTCAGATGCCAATCCCAAGTCCAGGTGTGGTCTGTGCTTCTGTCCAGCTG CAAGACGGCCCCCCATTCAGATGCCAATCCCACGTCCAGGTGTGGTCTGTGCTTCTGTCCAGCTG T G ZFYVE28 Ensembl:ENSG00000159733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs888344408 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 20457 RMVar_ID_20457 Human_SNP_ID_170750570 A-to-I Human chr4 - 2351102 2351102 2351102 AGTCCCACAAGACGGCCCCCCATTCAGATGCCAATCCCAAGTCCAGGTGTGGTCTGTGCTTCTGT AGTCCCACAAGACGGCCCCCCATTCAGATGCCGATCCCAAGTCCAGGTGTGGTCTGTGCTTCTGT T C ZFYVE28 Ensembl:ENSG00000159733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1447358415 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 20458 RMVar_ID_20458 Human_SNP_ID_170783800 A-to-I Human chr4 - 2468022 2468022 2468022 CACGCCCGGCTAATTTTCTTTGTATTTTTAGTAGAGATGGAGTTCCATCATGTTGGCCAGGCTGG CACGCCCGGCTAATTTTCTTTGTATTTTTAGTGGAGATGGAGTTCCATCATGTTGGCCAGGCTGG T C HSALNG0032378 RNACentral:URS0000EB922F lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1431877858 Functional Loss SNV dbSNP153 33..33 33 - - - 20459 RMVar_ID_20459 Human_SNP_ID_170785859 A-to-I Human chr4 + 2474310 2474310 2474310 TGAGGCAGGAGAATCGCTTGAACCCAGGAGGCAGAGGTTGCAGCGAGCCGAAATCACGCCATTGC TGAGGCAGGAGAATCGCTTGAACCCAGGAGGCGGAGGTTGCAGCGAGCCGAAATCACGCCATTGC A G RNF4 Ensembl:ENSG00000063978 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1188107042 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28096,RMVar_hsa_circ_124524,RMVar_hsa_circ_224355 20460 RMVar_ID_20460 Human_SNP_ID_170785871 A-to-I Human chr4 + 2474333 2474331 2474333 CCAGGAGGCAGAGGTTGCAGCGAGCCGAAATCACGCCATTGCACTCCATCCAGCCTGGTTGACAG CCAGGAGGCAGAGGTTGCAGCGAGCCGAAAT__CGCCATTGCACTCCATCCAGCCTGGTTGACAG TCA T RNF4 Ensembl:ENSG00000063978 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1363528618 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_28096,RMVar_hsa_circ_124524,RMVar_hsa_circ_224355 20461 RMVar_ID_20461 Human_SNP_ID_170785873 A-to-I Human chr4 + 2474333 2474333 2474333 CCAGGAGGCAGAGGTTGCAGCGAGCCGAAATCACGCCATTGCACTCCATCCAGCCTGGTTGACAG CCAGGAGGCAGAGGTTGCAGCGAGCCGAAATCGCGCCATTGCACTCCATCCAGCCTGGTTGACAG A G RNF4 Ensembl:ENSG00000063978 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432192189 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28096,RMVar_hsa_circ_124524,RMVar_hsa_circ_224355 20462 RMVar_ID_20462 Human_SNP_ID_170785995 A-to-I Human chr4 + 2474783 2474783 2474783 GCGGTGGCTCACGCCTGTAATCCCAGCACTTTAGGAGGCCGAGGCAGGCGGATCACCTCAGGTTG GCGGTGGCTCACGCCTGTAATCCCAGCACTTTCGGAGGCCGAGGCAGGCGGATCACCTCAGGTTG A C RNF4 Ensembl:ENSG00000063978 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1033399194 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28096,RMVar_hsa_circ_124524,RMVar_hsa_circ_224355 20463 RMVar_ID_20463 Human_SNP_ID_170786016 A-to-I Human chr4 + 2474863 2474863 2474863 CCTGGCCAACATGGAGAAACCCCGTCTCGACTAAAAATACAAAAAAATTAGCTGGGCGTGGTGGG CCTGGCCAACATGGAGAAACCCCGTCTCGACTGAAAATACAAAAAAATTAGCTGGGCGTGGTGGG A G RNF4 Ensembl:ENSG00000063978 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs186309931 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28096,RMVar_hsa_circ_124524,RMVar_hsa_circ_224355 20464 RMVar_ID_20464 Human_SNP_ID_170786017 A-to-I Human chr4 + 2474863 2474863 2474863 CCTGGCCAACATGGAGAAACCCCGTCTCGACTAAAAATACAAAAAAATTAGCTGGGCGTGGTGGG CCTGGCCAACATGGAGAAACCCCGTCTCGACTTAAAATACAAAAAAATTAGCTGGGCGTGGTGGG A T RNF4 Ensembl:ENSG00000063978 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs186309931 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28096,RMVar_hsa_circ_124524,RMVar_hsa_circ_224355 20465 RMVar_ID_20465 Human_SNP_ID_170786047 A-to-I Human chr4 + 2474959 2474959 2474959 TGAGACAGGAGAATTGCTTGAACCAGGGAGGCAGAGGTTGCGGTGAGCCAAGATTGCGCCGTTGT TGAGACAGGAGAATTGCTTGAACCAGGGAGGCGGAGGTTGCGGTGAGCCAAGATTGCGCCGTTGT A G RNF4 Ensembl:ENSG00000063978 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1381497496 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25804427 RMVar_hsa_circ_28096,RMVar_hsa_circ_124524,RMVar_hsa_circ_224355 20466 RMVar_ID_20466 Human_SNP_ID_170786183 A-to-I Human chr4 + 2475370 2475370 2475370 TGTTTGTTTGTTTGTTTTTGAGATGTAGTCTCACTCTGCCGCCCAGGCTGGTGTGCAGTGGCGCG TGTTTGTTTGTTTGTTTTTGAGATGTAGTCTCGCTCTGCCGCCCAGGCTGGTGTGCAGTGGCGCG A G RNF4 Ensembl:ENSG00000063978 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1377763654 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_619059 RMVar_hsa_circ_28096,RMVar_hsa_circ_124524,RMVar_hsa_circ_224355 20467 RMVar_ID_20467 Human_SNP_ID_170786527 A-to-I Human chr4 + 2476472 2476472 2476472 GCTGGAGTACAGTGGCACGATCTCAGCACTGCAACCTCTGCCTCCCGGGTTCAAGCAATTCTCCT GCTGGAGTACAGTGGCACGATCTCAGCACTGCGACCTCTGCCTCCCGGGTTCAAGCAATTCTCCT A G RNF4 Ensembl:ENSG00000063978 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1560399235 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15129878 RMVar_hsa_circ_28096,RMVar_hsa_circ_124524,RMVar_hsa_circ_224355 20468 RMVar_ID_20468 Human_SNP_ID_170786830 A-to-I Human chr4 + 2477438 2477438 2477438 GAAACCCTGTCTCTACTAAAAATACAAAAATTAGCTGGACATGGTGGTACATGCCTGTAGTTCCA GAAACCCTGTCTCTACTAAAAATACAAAAATTTGCTGGACATGGTGGTACATGCCTGTAGTTCCA A T RNF4 Ensembl:ENSG00000063978 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs919740600 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28096,RMVar_hsa_circ_124524,RMVar_hsa_circ_224355 20469 RMVar_ID_20469 Human_SNP_ID_170786858 A-to-I Human chr4 + 2477510 2477510 2477510 GGGAGGCTGAGGCAGGAGAATTGCTTGAACCCAGGAGGTGGAGATTACAGTGAGCCGAGATCATG GGGAGGCTGAGGCAGGAGAATTGCTTGAACCCGGGAGGTGGAGATTACAGTGAGCCGAGATCATG A G RNF4 Ensembl:ENSG00000063978 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs528078606 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28096,RMVar_hsa_circ_124524,RMVar_hsa_circ_224355 20470 RMVar_ID_20470 Human_SNP_ID_170786863 A-to-I Human chr4 + 2477524 2477524 2477524 GGAGAATTGCTTGAACCCAGGAGGTGGAGATTACAGTGAGCCGAGATCATGCCACTGCACTCCAG GGAGAATTGCTTGAACCCAGGAGGTGGAGATTGCAGTGAGCCGAGATCATGCCACTGCACTCCAG A G RNF4 Ensembl:ENSG00000063978 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1326462180 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28096,RMVar_hsa_circ_124524,RMVar_hsa_circ_224355 20471 RMVar_ID_20471 Human_SNP_ID_170786871 A-to-I Human chr4 + 2477540 2477540 2477540 CCAGGAGGTGGAGATTACAGTGAGCCGAGATCATGCCACTGCACTCCAGCTTGGACAACAGAGTA CCAGGAGGTGGAGATTACAGTGAGCCGAGATCGTGCCACTGCACTCCAGCTTGGACAACAGAGTA A G RNF4 Ensembl:ENSG00000063978 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1002577750 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28096,RMVar_hsa_circ_124524,RMVar_hsa_circ_224355 20472 RMVar_ID_20472 Human_SNP_ID_170788562 A-to-I Human chr4 + 2483665 2483665 2483665 ATCTCTACTAAAAATACAAAAATTAGCCGGGCATGGTGGTGGGTTCCTGTAATCCCAGCTAGTTG ATCTCTACTAAAAATACAAAAATTAGCCGGGCGTGGTGGTGGGTTCCTGTAATCCCAGCTAGTTG A G RNF4 Ensembl:ENSG00000063978 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1237456499 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28096,RMVar_hsa_circ_124524,RMVar_hsa_circ_224355 20473 RMVar_ID_20473 Human_SNP_ID_170788566 A-to-I Human chr4 + 2483683 2483683 2483683 AAAATTAGCCGGGCATGGTGGTGGGTTCCTGTAATCCCAGCTAGTTGGGAGGCTGAGGCACAAGA AAAATTAGCCGGGCATGGTGGTGGGTTCCTGTTATCCCAGCTAGTTGGGAGGCTGAGGCACAAGA A T RNF4 Ensembl:ENSG00000063978 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1293194959 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28096,RMVar_hsa_circ_124524,RMVar_hsa_circ_224355 20474 RMVar_ID_20474 Human_SNP_ID_170789996 A-to-I Human chr4 + 2488374 2488374 2488374 TAGTCCCAGCTACTGGGAGGCTGAGGCAGGAGAATCACTTGAACCTGGGAGGTGGAGGTTGCAGT TAGTCCCAGCTACTGGGAGGCTGAGGCAGGAGGATCACTTGAACCTGGGAGGTGGAGGTTGCAGT A G RNF4 Ensembl:ENSG00000063978 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1013133954 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28096,RMVar_hsa_circ_124524,RMVar_hsa_circ_224355 20475 RMVar_ID_20475 Human_SNP_ID_170790863 A-to-I Human chr4 + 2491354 2491354 2491354 CACGTTCTGGGTTCAAGTGATTCTTGTGCCTCAGCCTCCCACATAGCTGCGATTACAGGCATGCA CACGTTCTGGGTTCAAGTGATTCTTGTGCCTCGGCCTCCCACATAGCTGCGATTACAGGCATGCA A G RNF4 Ensembl:ENSG00000063978 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs996727732 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28096,RMVar_hsa_circ_124524,RMVar_hsa_circ_224355,RMVar_hsa_circ_224356,RMVar_hsa_circ_284304,RMVar_hsa_circ_285355,RMVar_hsa_circ_224357 20476 RMVar_ID_20476 Human_SNP_ID_170790939 A-to-I Human chr4 + 2491622 2491622 2491622 CTACCACCACACCCAGCTGATTTTGTATTTTTAGTAGAGATGTGATTTCACCATGTTGGCCAGGC CTACCACCACACCCAGCTGATTTTGTATTTTTGGTAGAGATGTGATTTCACCATGTTGGCCAGGC A G RNF4 Ensembl:ENSG00000063978 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs147686803 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28096,RMVar_hsa_circ_124524,RMVar_hsa_circ_224355,RMVar_hsa_circ_224356,RMVar_hsa_circ_284304,RMVar_hsa_circ_285355,RMVar_hsa_circ_224357 20477 RMVar_ID_20477 Human_SNP_ID_170790998 A-to-I Human chr4 + 2491873 2491873 2491873 CTTTCACCTCAGCATCCTGAGTAGTTGGGATCATAGGCATGCACCACCGCACCTGGCCAATTTTT CTTTCACCTCAGCATCCTGAGTAGTTGGGATCGTAGGCATGCACCACCGCACCTGGCCAATTTTT A G RNF4 Ensembl:ENSG00000063978 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1436081667 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28096,RMVar_hsa_circ_124524,RMVar_hsa_circ_224355,RMVar_hsa_circ_224356,RMVar_hsa_circ_284304,RMVar_hsa_circ_285355,RMVar_hsa_circ_224357 20478 RMVar_ID_20478 Human_SNP_ID_170791736 A-to-I Human chr4 + 2494503 2494503 2494503 GGGTTCACACCATTCTCCTGCCGCAGCCTCCCAAGTAGCTGGGACTACAGGTGCCCGCCACCACG GGGTTCACACCATTCTCCTGCCGCAGCCTCCCGAGTAGCTGGGACTACAGGTGCCCGCCACCACG A G RNF4 Ensembl:ENSG00000063978 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1168940660 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28096,RMVar_hsa_circ_124524,RMVar_hsa_circ_224355,RMVar_hsa_circ_224356,RMVar_hsa_circ_284304,RMVar_hsa_circ_285355,RMVar_hsa_circ_224357 20479 RMVar_ID_20479 Human_SNP_ID_170791774 A-to-I Human chr4 + 2494587 2494587 2494587 ATTTTTTAGTAGAGATGGGGTTTCTACGTGTTAGCCAGGATGGTCTCGATCTTCTGACCTTGTGA ATTTTTTAGTAGAGATGGGGTTTCTACGTGTTGGCCAGGATGGTCTCGATCTTCTGACCTTGTGA A G RNF4 Ensembl:ENSG00000063978 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs888323341 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15130177 Human_Splice_Rec_539600,Human_Splice_Rec_539628 RMVar_hsa_circ_28096,RMVar_hsa_circ_124524,RMVar_hsa_circ_224355,RMVar_hsa_circ_224356,RMVar_hsa_circ_284304,RMVar_hsa_circ_285355,RMVar_hsa_circ_224357 20480 RMVar_ID_20480 Human_SNP_ID_170791796 A-to-I Human chr4 + 2494632 2494632 2494632 TCGATCTTCTGACCTTGTGATCCGCCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGCG TCGATCTTCTGACCTTGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGCG A G RNF4 Ensembl:ENSG00000063978 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1289682176 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_539600,Human_Splice_Rec_539628 RMVar_hsa_circ_28096,RMVar_hsa_circ_124524,RMVar_hsa_circ_224355,RMVar_hsa_circ_224356,RMVar_hsa_circ_284304,RMVar_hsa_circ_285355,RMVar_hsa_circ_224357 20481 RMVar_ID_20481 Human_SNP_ID_170792883 A-to-I Human chr4 + 2498239 2498239 2498239 AGAGTTTCGTTCTGTCAGCCAGGTTGGAGTGCAATCGCGTGATCTCGGCTCACTGCAACCTCTGC AGAGTTTCGTTCTGTCAGCCAGGTTGGAGTGCCATCGCGTGATCTCGGCTCACTGCAACCTCTGC A C RNF4 Ensembl:ENSG00000063978 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs935448539 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28096,RMVar_hsa_circ_124524,RMVar_hsa_circ_224355,RMVar_hsa_circ_284304,RMVar_hsa_circ_224357,RMVar_hsa_circ_224358,RMVar_hsa_circ_309590 20482 RMVar_ID_20482 Human_SNP_ID_170792929 A-to-I Human chr4 + 2498393 2498393 2498393 TATTTTTAGTAGAGACGGGGTTTCACCATGTCAGTCAGGCTGATCTCGAACTCCTGACCTCAGAT TATTTTTAGTAGAGACGGGGTTTCACCATGTCGGTCAGGCTGATCTCGAACTCCTGACCTCAGAT A G RNF4 Ensembl:ENSG00000063978 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1385925571 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28096,RMVar_hsa_circ_124524,RMVar_hsa_circ_224355,RMVar_hsa_circ_284304,RMVar_hsa_circ_224357,RMVar_hsa_circ_224358,RMVar_hsa_circ_309590 20483 RMVar_ID_20483 Human_SNP_ID_170793022 A-to-I Human chr4 + 2498742 2498742 2498742 GCCCAGGAGTACCAGACCAGCCTGGACAACATAGTGAGACCCTGTCTCTATAAATAAAAAAATTA GCCCAGGAGTACCAGACCAGCCTGGACAACATCGTGAGACCCTGTCTCTATAAATAAAAAAATTA A C RNF4 Ensembl:ENSG00000063978 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs146749291 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28096,RMVar_hsa_circ_124524,RMVar_hsa_circ_224355,RMVar_hsa_circ_284304,RMVar_hsa_circ_224357,RMVar_hsa_circ_224358,RMVar_hsa_circ_309590 20484 RMVar_ID_20484 Human_SNP_ID_170793091 A-to-I Human chr4 + 2498939 2498939 2498939 TTACGTTGGGTTGGGCGCCATGGCTGGCTCCTATAATCCCAGCACTTTGGGAGGCCGAGGCGTGC TTACGTTGGGTTGGGCGCCATGGCTGGCTCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGTGC A G RNF4 Ensembl:ENSG00000063978 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs868815103 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28096,RMVar_hsa_circ_124524,RMVar_hsa_circ_224355,RMVar_hsa_circ_284304,RMVar_hsa_circ_224357,RMVar_hsa_circ_224358,RMVar_hsa_circ_309590 20485 RMVar_ID_20485 Human_SNP_ID_170793110 A-to-I Human chr4 + 2498995 2498995 2498995 GAGGCGTGCAGATCACCTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGGCGAAACCCCAT GAGGCGTGCAGATCACCTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGCGAAACCCCAT A G RNF4 Ensembl:ENSG00000063978 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs28408405 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28096,RMVar_hsa_circ_124524,RMVar_hsa_circ_224355,RMVar_hsa_circ_284304,RMVar_hsa_circ_224357,RMVar_hsa_circ_224358,RMVar_hsa_circ_309590 20486 RMVar_ID_20486 Human_SNP_ID_170794294 A-to-I Human chr4 + 2503143 2503143 2503143 AGCAGTCACCCACCTCAGCCTCCCAAAGCACTAGGATTACAGGTGTGAGCCACCACACTGGCCAG AGCAGTCACCCACCTCAGCCTCCCAAAGCACTGGGATTACAGGTGTGAGCCACCACACTGGCCAG A G RNF4 Ensembl:ENSG00000063978 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs911262549 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124524,RMVar_hsa_circ_224355 20487 RMVar_ID_20487 Human_SNP_ID_170806221 A-to-I Human chr4 + 2539540 2539540 2539540 ATTTCTGGGCTAAGCAGTCCTTCCATGTAGCTAGGCCTCTAGGTATGTGCCACCATGCCTGGCTA ATTTCTGGGCTAAGCAGTCCTTCCATGTAGCTTGGCCTCTAGGTATGTGCCACCATGCCTGGCTA A T FAM193A,RNF4 Ensembl:ENSG00000125386,Ensembl:ENSG00000063978 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1236934145 Functional Loss SNV dbSNP153 33..33 33 - - - 20488 RMVar_ID_20488 Human_SNP_ID_170808386 A-to-I Human chr4 + 2546014 2546009 2546014 TACTAAAAATACAAAAATTAGCGGGGTGTGGTAGCAGGCGCCTGTAATCATAGCTACTCGGGAGG TACTAAAAATACAAAAATTAGCGGGGTG_____GCAGGCGCCTGTAATCATAGCTACTCGGGAGG GTGGTA G FAM193A,RNF4 Ensembl:ENSG00000125386,Ensembl:ENSG00000063978 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170430614 Functional Loss DEL dbSNP153 29..33 33 - - - 20489 RMVar_ID_20489 Human_SNP_ID_170808389 A-to-I Human chr4 + 2546014 2546014 2546014 TACTAAAAATACAAAAATTAGCGGGGTGTGGTAGCAGGCGCCTGTAATCATAGCTACTCGGGAGG TACTAAAAATACAAAAATTAGCGGGGTGTGGTGGCAGGCGCCTGTAATCATAGCTACTCGGGAGG A G FAM193A,RNF4 Ensembl:ENSG00000125386,Ensembl:ENSG00000063978 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256883121 Functional Loss SNV dbSNP153 33..33 33 - - - 20490 RMVar_ID_20490 Human_SNP_ID_170808849 A-to-I Human chr4 + 2547524 2547524 2547524 TCCTCCCACCTTGGCTTCCCAGTGTTAGGATTACAGGCGTGAGCCACCGCACCCAGCCTAAAACT TCCTCCCACCTTGGCTTCCCAGTGTTAGGATTGCAGGCGTGAGCCACCGCACCCAGCCTAAAACT A G FAM193A,RNF4 Ensembl:ENSG00000125386,Ensembl:ENSG00000063978 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs528533201 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23313290 20491 RMVar_ID_20491 Human_SNP_ID_170811534 A-to-I Human chr4 + 2555545 2555545 2555545 TTACAACCATAATCCTAACACTTTGGGAGGCCAAGGCAGGAGGATCCCTTGAGCCCGGGATTTTG TTACAACCATAATCCTAACACTTTGGGAGGCCGAGGCAGGAGGATCCCTTGAGCCCGGGATTTTG A G FAM193A,RNF4 Ensembl:ENSG00000125386,Ensembl:ENSG00000063978 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1246065087 Functional Loss SNV dbSNP153 33..33 33 - - - 20492 RMVar_ID_20492 Human_SNP_ID_170811876 A-to-I Human chr4 + 2556548 2556548 2556548 TTACAAAATAAAAGAAGGGAGTCAGGTGTGGTAGTGTGCACCCACAGTTCTAGCTACTCAGGAGG TTACAAAATAAAAGAAGGGAGTCAGGTGTGGTGGTGTGCACCCACAGTTCTAGCTACTCAGGAGG A G FAM193A,RNF4 Ensembl:ENSG00000125386,Ensembl:ENSG00000063978 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs572861127 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17574702 20493 RMVar_ID_20493 Human_SNP_ID_170812433 A-to-I Human chr4 + 2558521 2558521 2558521 CTCCCACGTCAGGCTTTCAAGTACCTGGGACTACAGGCACGGGCCACCACACCCAGCTAATCAAA CTCCCACGTCAGGCTTTCAAGTACCTGGGACTGCAGGCACGGGCCACCACACCCAGCTAATCAAA A G FAM193A,RNF4 Ensembl:ENSG00000125386,Ensembl:ENSG00000063978 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs573601435 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17574594 20494 RMVar_ID_20494 Human_SNP_ID_170814293 A-to-I Human chr4 + 2564828 2564828 2564828 TTTTTTTTGTTCTTGTTTTTTATTTTTGAGATAGGGACTCACTCTTGTCGCCCAGGTTGGAGGGC TTTTTTTTGTTCTTGTTTTTTATTTTTGAGATCGGGACTCACTCTTGTCGCCCAGGTTGGAGGGC A C FAM193A,RNF4 Ensembl:ENSG00000125386,Ensembl:ENSG00000063978 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs530773238 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7302199,Human_RBP_ID_15132902 20495 RMVar_ID_20495 Human_SNP_ID_170814294 A-to-I Human chr4 + 2564828 2564828 2564828 TTTTTTTTGTTCTTGTTTTTTATTTTTGAGATAGGGACTCACTCTTGTCGCCCAGGTTGGAGGGC TTTTTTTTGTTCTTGTTTTTTATTTTTGAGATGGGGACTCACTCTTGTCGCCCAGGTTGGAGGGC A G FAM193A,RNF4 Ensembl:ENSG00000125386,Ensembl:ENSG00000063978 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs530773238 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7302199,Human_RBP_ID_15132902 20496 RMVar_ID_20496 Human_SNP_ID_170814896 A-to-I Human chr4 + 2566567 2566567 2566567 AAAATTAGCTGGACGTGGTGGTGTGCGCCTGTAGTCCCCAGCTACTCGGGAGGCTGAGGCAGGAG AAAATTAGCTGGACGTGGTGGTGTGCGCCTGTGGTCCCCAGCTACTCGGGAGGCTGAGGCAGGAG A G FAM193A,RNF4 Ensembl:ENSG00000125386,Ensembl:ENSG00000063978 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1318863802 Functional Loss SNV dbSNP153 33..33 33 - - - 20497 RMVar_ID_20497 Human_SNP_ID_170815455 A-to-I Human chr4 + 2568459 2568459 2568459 GGAGGATCACCTGAGCCCAGGAGTTGCAGGCTACAGTGAGCTGTGATTGTGTCATTGCACTTCAG GGAGGATCACCTGAGCCCAGGAGTTGCAGGCTGCAGTGAGCTGTGATTGTGTCATTGCACTTCAG A G FAM193A,RNF4 Ensembl:ENSG00000125386,Ensembl:ENSG00000063978 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1242711929 Functional Loss SNV dbSNP153 33..33 33 - - - 20498 RMVar_ID_20498 Human_SNP_ID_170835714 A-to-I Human chr4 + 2636072 2636071 2636073 AATAATTTGTCTTTTTGTGTTTTTTTTGAGACAGAGTCTCACTCTGTCTCAAAAAAAAATCTCGC AATAATTTGTCTTTTTGTGTTTTTTTTGAGAC__AGTCTCACTCTGTCTCAAAAAAAAATCTCGC CAG C FAM193A Ensembl:ENSG00000125386 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1184872840 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_12150,RMVar_hsa_circ_26985,RMVar_hsa_circ_73467,RMVar_hsa_circ_308286,RMVar_hsa_circ_356592,RMVar_hsa_circ_295975,RMVar_hsa_circ_296060,RMVar_hsa_circ_224360,RMVar_hsa_circ_68174,RMVar_hsa_circ_68554,RMVar_hsa_circ_34214,RMVar_hsa_circ_282087,RMVar_hsa_circ_307806,RMVar_hsa_circ_373640,RMVar_hsa_circ_327988,RMVar_hsa_circ_292767,RMVar_hsa_circ_280027,RMVar_hsa_circ_104881,RMVar_hsa_circ_224361,RMVar_hsa_circ_224363,RMVar_hsa_circ_224362,RMVar_hsa_circ_91581,RMVar_hsa_circ_224366,RMVar_hsa_circ_293587,RMVar_hsa_circ_224367,RMVar_hsa_circ_299485,RMVar_hsa_circ_20241,RMVar_hsa_circ_224369,RMVar_hsa_circ_224370 20499 RMVar_ID_20499 Human_SNP_ID_170835715 A-to-I Human chr4 + 2636072 2636072 2636072 AATAATTTGTCTTTTTGTGTTTTTTTTGAGACAGAGTCTCACTCTGTCTCAAAAAAAAATCTCGC AATAATTTGTCTTTTTGTGTTTTTTTTGAGACGGAGTCTCACTCTGTCTCAAAAAAAAATCTCGC A G FAM193A Ensembl:ENSG00000125386 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1489188278 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12150,RMVar_hsa_circ_26985,RMVar_hsa_circ_73467,RMVar_hsa_circ_308286,RMVar_hsa_circ_356592,RMVar_hsa_circ_295975,RMVar_hsa_circ_296060,RMVar_hsa_circ_224360,RMVar_hsa_circ_68174,RMVar_hsa_circ_68554,RMVar_hsa_circ_34214,RMVar_hsa_circ_282087,RMVar_hsa_circ_307806,RMVar_hsa_circ_373640,RMVar_hsa_circ_327988,RMVar_hsa_circ_292767,RMVar_hsa_circ_280027,RMVar_hsa_circ_104881,RMVar_hsa_circ_224361,RMVar_hsa_circ_224363,RMVar_hsa_circ_224362,RMVar_hsa_circ_91581,RMVar_hsa_circ_224366,RMVar_hsa_circ_293587,RMVar_hsa_circ_224367,RMVar_hsa_circ_299485,RMVar_hsa_circ_20241,RMVar_hsa_circ_224369,RMVar_hsa_circ_224370 20500 RMVar_ID_20500 Human_SNP_ID_170837007 A-to-I Human chr4 + 2640786 2640786 2640786 CAGGAGTTTGAGACCAGCCTTGCCAACATGGTAAAACCCCGTCTCTACTAAAAATATAAAAATTA CAGGAGTTTGAGACCAGCCTTGCCAACATGGTCAAACCCCGTCTCTACTAAAAATATAAAAATTA A C FAM193A Ensembl:ENSG00000125386 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1040336968 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12150,RMVar_hsa_circ_26985,RMVar_hsa_circ_73467,RMVar_hsa_circ_308286,RMVar_hsa_circ_356592,RMVar_hsa_circ_295975,RMVar_hsa_circ_68174,RMVar_hsa_circ_68554,RMVar_hsa_circ_34214,RMVar_hsa_circ_282087,RMVar_hsa_circ_307806,RMVar_hsa_circ_373640,RMVar_hsa_circ_327988,RMVar_hsa_circ_292767,RMVar_hsa_circ_104881,RMVar_hsa_circ_224361,RMVar_hsa_circ_224362,RMVar_hsa_circ_91581,RMVar_hsa_circ_224366,RMVar_hsa_circ_293587,RMVar_hsa_circ_224367,RMVar_hsa_circ_20241,RMVar_hsa_circ_18679,RMVar_hsa_circ_224371,RMVar_hsa_circ_224370,RMVar_hsa_circ_75128,RMVar_hsa_circ_301140,RMVar_hsa_circ_357582,RMVar_hsa_circ_38281 20501 RMVar_ID_20501 Human_SNP_ID_170837145 A-to-I Human chr4 + 2641230 2641230 2641230 CACCACGCCTGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGGTGG CACCACGCCTGGCTAATTTTTGTATTTTTAGTGGAGACGGGGTTTCACCATGTTGGCCAGGGTGG A G FAM193A Ensembl:ENSG00000125386 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1049070908 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12150,RMVar_hsa_circ_26985,RMVar_hsa_circ_73467,RMVar_hsa_circ_308286,RMVar_hsa_circ_356592,RMVar_hsa_circ_295975,RMVar_hsa_circ_68174,RMVar_hsa_circ_68554,RMVar_hsa_circ_34214,RMVar_hsa_circ_282087,RMVar_hsa_circ_307806,RMVar_hsa_circ_373640,RMVar_hsa_circ_327988,RMVar_hsa_circ_292767,RMVar_hsa_circ_104881,RMVar_hsa_circ_224361,RMVar_hsa_circ_224362,RMVar_hsa_circ_91581,RMVar_hsa_circ_224366,RMVar_hsa_circ_293587,RMVar_hsa_circ_224367,RMVar_hsa_circ_20241,RMVar_hsa_circ_18679,RMVar_hsa_circ_224371,RMVar_hsa_circ_224370,RMVar_hsa_circ_75128,RMVar_hsa_circ_301140,RMVar_hsa_circ_357582,RMVar_hsa_circ_38281 20502 RMVar_ID_20502 Human_SNP_ID_170837172 A-to-I Human chr4 + 2641315 2641315 2641315 GTGATCCACCTGCCTCAGCCTCCCAAAGTGCTAGGATTACAGGCATGACCCACCATGCCCAATCT GTGATCCACCTGCCTCAGCCTCCCAAAGTGCTCGGATTACAGGCATGACCCACCATGCCCAATCT A C FAM193A Ensembl:ENSG00000125386 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053426164 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12150,RMVar_hsa_circ_26985,RMVar_hsa_circ_73467,RMVar_hsa_circ_308286,RMVar_hsa_circ_356592,RMVar_hsa_circ_295975,RMVar_hsa_circ_68174,RMVar_hsa_circ_68554,RMVar_hsa_circ_34214,RMVar_hsa_circ_282087,RMVar_hsa_circ_307806,RMVar_hsa_circ_373640,RMVar_hsa_circ_327988,RMVar_hsa_circ_292767,RMVar_hsa_circ_104881,RMVar_hsa_circ_224361,RMVar_hsa_circ_224362,RMVar_hsa_circ_91581,RMVar_hsa_circ_224366,RMVar_hsa_circ_293587,RMVar_hsa_circ_224367,RMVar_hsa_circ_20241,RMVar_hsa_circ_18679,RMVar_hsa_circ_224371,RMVar_hsa_circ_224370,RMVar_hsa_circ_75128,RMVar_hsa_circ_301140,RMVar_hsa_circ_357582,RMVar_hsa_circ_38281 20503 RMVar_ID_20503 Human_SNP_ID_170837252 A-to-I Human chr4 + 2641508 2641508 2641508 AAACCTCGTCTCTACTAAAAATACAAAAAATTAGCCGGGCGTAGTGGCGCATGCCTGTAGTCCCA AAACCTCGTCTCTACTAAAAATACAAAAAATTTGCCGGGCGTAGTGGCGCATGCCTGTAGTCCCA A T FAM193A Ensembl:ENSG00000125386 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1043032266 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12150,RMVar_hsa_circ_26985,RMVar_hsa_circ_73467,RMVar_hsa_circ_308286,RMVar_hsa_circ_356592,RMVar_hsa_circ_295975,RMVar_hsa_circ_68174,RMVar_hsa_circ_68554,RMVar_hsa_circ_34214,RMVar_hsa_circ_282087,RMVar_hsa_circ_307806,RMVar_hsa_circ_373640,RMVar_hsa_circ_327988,RMVar_hsa_circ_292767,RMVar_hsa_circ_104881,RMVar_hsa_circ_224361,RMVar_hsa_circ_224362,RMVar_hsa_circ_91581,RMVar_hsa_circ_224366,RMVar_hsa_circ_293587,RMVar_hsa_circ_224367,RMVar_hsa_circ_20241,RMVar_hsa_circ_18679,RMVar_hsa_circ_224371,RMVar_hsa_circ_224370,RMVar_hsa_circ_75128,RMVar_hsa_circ_301140,RMVar_hsa_circ_357582,RMVar_hsa_circ_38281 20504 RMVar_ID_20504 Human_SNP_ID_170837259 A-to-I Human chr4 + 2641518 2641518 2641518 TCTACTAAAAATACAAAAAATTAGCCGGGCGTAGTGGCGCATGCCTGTAGTCCCAGCTACTTGGG TCTACTAAAAATACAAAAAATTAGCCGGGCGTGGTGGCGCATGCCTGTAGTCCCAGCTACTTGGG A G FAM193A Ensembl:ENSG00000125386 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1225484965 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12150,RMVar_hsa_circ_26985,RMVar_hsa_circ_73467,RMVar_hsa_circ_308286,RMVar_hsa_circ_356592,RMVar_hsa_circ_295975,RMVar_hsa_circ_68174,RMVar_hsa_circ_68554,RMVar_hsa_circ_34214,RMVar_hsa_circ_282087,RMVar_hsa_circ_307806,RMVar_hsa_circ_373640,RMVar_hsa_circ_327988,RMVar_hsa_circ_292767,RMVar_hsa_circ_104881,RMVar_hsa_circ_224361,RMVar_hsa_circ_224362,RMVar_hsa_circ_91581,RMVar_hsa_circ_224366,RMVar_hsa_circ_293587,RMVar_hsa_circ_224367,RMVar_hsa_circ_20241,RMVar_hsa_circ_18679,RMVar_hsa_circ_224371,RMVar_hsa_circ_224370,RMVar_hsa_circ_75128,RMVar_hsa_circ_301140,RMVar_hsa_circ_357582,RMVar_hsa_circ_38281 20505 RMVar_ID_20505 Human_SNP_ID_170840086 A-to-I Human chr4 + 2651088 2651088 2651088 GCTTGATACTCACCCCTGTAATCCCAGCACTTAGGGAGGCCAAGGTGGGCGGATCACCTGAGGTC GCTTGATACTCACCCCTGTAATCCCAGCACTTCGGGAGGCCAAGGTGGGCGGATCACCTGAGGTC A C FAM193A Ensembl:ENSG00000125386 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1304531650 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12150,RMVar_hsa_circ_26985,RMVar_hsa_circ_73467,RMVar_hsa_circ_308286,RMVar_hsa_circ_356592,RMVar_hsa_circ_68174,RMVar_hsa_circ_68554,RMVar_hsa_circ_34214,RMVar_hsa_circ_282087,RMVar_hsa_circ_307806,RMVar_hsa_circ_373640,RMVar_hsa_circ_327988,RMVar_hsa_circ_104881,RMVar_hsa_circ_224361,RMVar_hsa_circ_224367,RMVar_hsa_circ_20241,RMVar_hsa_circ_18679,RMVar_hsa_circ_75128,RMVar_hsa_circ_301140,RMVar_hsa_circ_357582,RMVar_hsa_circ_18552,RMVar_hsa_circ_266476,RMVar_hsa_circ_347013,RMVar_hsa_circ_377394,RMVar_hsa_circ_301775,RMVar_hsa_circ_67890,RMVar_hsa_circ_6280 20506 RMVar_ID_20506 Human_SNP_ID_170840087 A-to-I Human chr4 + 2651088 2651088 2651088 GCTTGATACTCACCCCTGTAATCCCAGCACTTAGGGAGGCCAAGGTGGGCGGATCACCTGAGGTC GCTTGATACTCACCCCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGCGGATCACCTGAGGTC A T FAM193A Ensembl:ENSG00000125386 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1304531650 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12150,RMVar_hsa_circ_26985,RMVar_hsa_circ_73467,RMVar_hsa_circ_308286,RMVar_hsa_circ_356592,RMVar_hsa_circ_68174,RMVar_hsa_circ_68554,RMVar_hsa_circ_34214,RMVar_hsa_circ_282087,RMVar_hsa_circ_307806,RMVar_hsa_circ_373640,RMVar_hsa_circ_327988,RMVar_hsa_circ_104881,RMVar_hsa_circ_224361,RMVar_hsa_circ_224367,RMVar_hsa_circ_20241,RMVar_hsa_circ_18679,RMVar_hsa_circ_75128,RMVar_hsa_circ_301140,RMVar_hsa_circ_357582,RMVar_hsa_circ_18552,RMVar_hsa_circ_266476,RMVar_hsa_circ_347013,RMVar_hsa_circ_377394,RMVar_hsa_circ_301775,RMVar_hsa_circ_67890,RMVar_hsa_circ_6280 20507 RMVar_ID_20507 Human_SNP_ID_170840862 A-to-I Human chr4 + 2653702 2653702 2653702 TTGACCTCATCATCCACCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCATG TTGACCTCATCATCCACCCACCTCAGCCTCCCGAAGTGCTGGGATTACAGGCGTGAGCCACCATG A G FAM193A Ensembl:ENSG00000125386 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1308951633 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12150,RMVar_hsa_circ_26985,RMVar_hsa_circ_73467,RMVar_hsa_circ_308286,RMVar_hsa_circ_356592,RMVar_hsa_circ_68174,RMVar_hsa_circ_68554,RMVar_hsa_circ_34214,RMVar_hsa_circ_282087,RMVar_hsa_circ_307806,RMVar_hsa_circ_373640,RMVar_hsa_circ_327988,RMVar_hsa_circ_104881,RMVar_hsa_circ_224361,RMVar_hsa_circ_224367,RMVar_hsa_circ_20241,RMVar_hsa_circ_18679,RMVar_hsa_circ_75128,RMVar_hsa_circ_301140,RMVar_hsa_circ_357582,RMVar_hsa_circ_18552,RMVar_hsa_circ_266476,RMVar_hsa_circ_347013,RMVar_hsa_circ_377394,RMVar_hsa_circ_301775,RMVar_hsa_circ_67890,RMVar_hsa_circ_6280 20508 RMVar_ID_20508 Human_SNP_ID_170843982 A-to-I Human chr4 + 2664823 2664823 2664823 CTGACCTTGTGATCCGCCCGTGTTGGCCTCCCAAAGTCCTGGGATTACAAGCGTGAGCCACTGCA CTGACCTTGTGATCCGCCCGTGTTGGCCTCCCTAAGTCCTGGGATTACAAGCGTGAGCCACTGCA A T FAM193A Ensembl:ENSG00000125386 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1326188454 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15136016,Human_RBP_ID_25805676 RMVar_hsa_circ_12150,RMVar_hsa_circ_73467,RMVar_hsa_circ_308286,RMVar_hsa_circ_356592,RMVar_hsa_circ_68554,RMVar_hsa_circ_373640,RMVar_hsa_circ_327988,RMVar_hsa_circ_104881,RMVar_hsa_circ_224361,RMVar_hsa_circ_224367,RMVar_hsa_circ_2714,RMVar_hsa_circ_75128,RMVar_hsa_circ_357582,RMVar_hsa_circ_18552,RMVar_hsa_circ_266476,RMVar_hsa_circ_67890,RMVar_hsa_circ_65572,RMVar_hsa_circ_6280,RMVar_hsa_circ_121326,RMVar_hsa_circ_281668,RMVar_hsa_circ_307706,RMVar_hsa_circ_347536,RMVar_hsa_circ_343600,RMVar_hsa_circ_280011,RMVar_hsa_circ_224374,RMVar_hsa_circ_224375,RMVar_hsa_circ_224373,RMVar_hsa_circ_29086,RMVar_hsa_circ_224380,RMVar_hsa_circ_269891,RMVar_hsa_circ_38026,RMVar_hsa_circ_268752,RMVar_hsa_circ_224381 20509 RMVar_ID_20509 Human_SNP_ID_170855078 A-to-I Human chr4 + 2703302 2703302 2703302 GGAGTCTCACTCTGTCATCTAGGCTGGAGTGCAATGGCGCAATCTCGGCTCACTGCATCCTCCAC GGAGTCTCACTCTGTCATCTAGGCTGGAGTGCGATGGCGCAATCTCGGCTCACTGCATCCTCCAC A G FAM193A Ensembl:ENSG00000125386 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs56091370 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_68554,RMVar_hsa_circ_75128,RMVar_hsa_circ_67890,RMVar_hsa_circ_65572,RMVar_hsa_circ_307706,RMVar_hsa_circ_224373,RMVar_hsa_circ_38026,RMVar_hsa_circ_56234,RMVar_hsa_circ_268752,RMVar_hsa_circ_62263,RMVar_hsa_circ_348051,RMVar_hsa_circ_224385,RMVar_hsa_circ_296555,RMVar_hsa_circ_224386 20510 RMVar_ID_20510 Human_SNP_ID_170855110 A-to-I Human chr4 + 2703386 2703386 2703386 CTCCCACCTCAGCCTCCCAAGTAGCTGAAATTACAGGCACGTGCCACCATACCCAGCTAATTTTT CTCCCACCTCAGCCTCCCAAGTAGCTGAAATTGCAGGCACGTGCCACCATACCCAGCTAATTTTT A G FAM193A Ensembl:ENSG00000125386 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1172177483 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_68554,RMVar_hsa_circ_75128,RMVar_hsa_circ_67890,RMVar_hsa_circ_65572,RMVar_hsa_circ_307706,RMVar_hsa_circ_224373,RMVar_hsa_circ_38026,RMVar_hsa_circ_56234,RMVar_hsa_circ_268752,RMVar_hsa_circ_62263,RMVar_hsa_circ_348051,RMVar_hsa_circ_224385,RMVar_hsa_circ_296555,RMVar_hsa_circ_224386 20511 RMVar_ID_20511 Human_SNP_ID_170855132 A-to-I Human chr4 + 2703494 2703494 2703494 GCCTTGAACTCCTGACCTTAAGTGACCTGCCCACCTTGGCCTCCCAAAGTGCTGGGATTACAGGT GCCTTGAACTCCTGACCTTAAGTGACCTGCCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGT A G FAM193A Ensembl:ENSG00000125386 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1198748514 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_68554,RMVar_hsa_circ_75128,RMVar_hsa_circ_67890,RMVar_hsa_circ_65572,RMVar_hsa_circ_307706,RMVar_hsa_circ_224373,RMVar_hsa_circ_38026,RMVar_hsa_circ_56234,RMVar_hsa_circ_268752,RMVar_hsa_circ_62263,RMVar_hsa_circ_348051,RMVar_hsa_circ_224385,RMVar_hsa_circ_296555,RMVar_hsa_circ_224386 20512 RMVar_ID_20512 Human_SNP_ID_170855852 A-to-I Human chr4 + 2705840 2705840 2705840 TAACTCCTGGGCTAAAGCAGTCCTCCTGCCTCAGCCTCCCACAGTGCTGGGATCACAGACGTGAG TAACTCCTGGGCTAAAGCAGTCCTCCTGCCTCTGCCTCCCACAGTGCTGGGATCACAGACGTGAG A T FAM193A Ensembl:ENSG00000125386 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1213805039 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_68554,RMVar_hsa_circ_75128,RMVar_hsa_circ_67890,RMVar_hsa_circ_65572,RMVar_hsa_circ_307706,RMVar_hsa_circ_224373,RMVar_hsa_circ_38026,RMVar_hsa_circ_56234,RMVar_hsa_circ_268752,RMVar_hsa_circ_62263,RMVar_hsa_circ_348051,RMVar_hsa_circ_224385,RMVar_hsa_circ_296555,RMVar_hsa_circ_224386 20513 RMVar_ID_20513 Human_SNP_ID_170860104 A-to-I Human chr4 + 2719997 2719997 2719997 TTCTTCTTTTTGTAGAGACGGGGTTTCGCCACATTGCCCAGGCTGGTCTCGAACTCCTGGCCTCA TTCTTCTTTTTGTAGAGACGGGGTTTCGCCACGTTGCCCAGGCTGGTCTCGAACTCCTGGCCTCA A G FAM193A Ensembl:ENSG00000125386 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1451213662 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_539746,Human_Splice_Rec_539952,Human_Splice_Rec_539953 20514 RMVar_ID_20514 Human_SNP_ID_170860228 A-to-I Human chr4 + 2720468 2720468 2720468 GAGCCCAGGAGTTTGAGACCAGCCTGAGCAACATAGCAAGATACTGTCTCTACAAAAAATAAAAT GAGCCCAGGAGTTTGAGACCAGCCTGAGCAACGTAGCAAGATACTGTCTCTACAAAAAATAAAAT A G FAM193A Ensembl:ENSG00000125386 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1359312638 Functional Loss SNV dbSNP153 33..33 33 - - - 20515 RMVar_ID_20515 Human_SNP_ID_170861118 A-to-I Human chr4 + 2723428 2723428 2723428 GAAACCCCCTCTCTACTGAAAATACAAAAATTAGCAAGATGTGGTGGTGGGTGCCTGTAATCCCA GAAACCCCCTCTCTACTGAAAATACAAAAATTGGCAAGATGTGGTGGTGGGTGCCTGTAATCCCA A G FAM193A Ensembl:ENSG00000125386 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900502927 Functional Loss SNV dbSNP153 33..33 33 - - - 20516 RMVar_ID_20516 Human_SNP_ID_170894883 A-to-I Human chr4 + 2833829 2833829 2833829 TGCTGCGGCACCCCTACGGCTACACTGGGCCTAGGTGATGGCAGTCCATGTGGCTGCCAGGCCAA TGCTGCGGCACCCCTACGGCTACACTGGGCCTGGGTGATGGCAGTCCATGTGGCTGCCAGGCCAA A G SH3BP2 Ensembl:ENSG00000087266 Protein coding CDS GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs11542558 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89980,RMVar_hsa_circ_224397 20517 RMVar_ID_20517 Human_SNP_ID_170896352 A-to-I Human chr4 + 2839592 2839592 2839592 GTCCTTTTTTTTTGGGGGGGGTTTTTTGAGACAAGGTCTTGCTCTGTCACCCAGGCTGGAGTGTT GTCCTTTTTTTTTGGGGGGGGTTTTTTGAGACGAGGTCTTGCTCTGTCACCCAGGCTGGAGTGTT A G SH3BP2 Ensembl:ENSG00000087266 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1220159528 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26791506 RMVar_hsa_circ_89980,RMVar_hsa_circ_224397 20518 RMVar_ID_20518 Human_SNP_ID_170896361 A-to-I Human chr4 + 2839625 2839625 2839625 AGGTCTTGCTCTGTCACCCAGGCTGGAGTGTTATGGCACAATCTTGGCTTATTGCAGCCTCAATT AGGTCTTGCTCTGTCACCCAGGCTGGAGTGTTGTGGCACAATCTTGGCTTATTGCAGCCTCAATT A G SH3BP2 Ensembl:ENSG00000087266 Protein coding 3'UTR GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs1295854052 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89980,RMVar_hsa_circ_224397 20519 RMVar_ID_20519 Human_SNP_ID_170896364 A-to-I Human chr4 + 2839632 2839632 2839632 GCTCTGTCACCCAGGCTGGAGTGTTATGGCACAATCTTGGCTTATTGCAGCCTCAATTCCTAGGC GCTCTGTCACCCAGGCTGGAGTGTTATGGCACGATCTTGGCTTATTGCAGCCTCAATTCCTAGGC A G SH3BP2 Ensembl:ENSG00000087266 Protein coding 3'UTR GSE38233;GSE100210;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,29129909,31158229,31158229,31158229,31158229 RNA-Seq:(High) rs1399738828 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89980,RMVar_hsa_circ_224397 20520 RMVar_ID_20520 Human_SNP_ID_170896373 A-to-I Human chr4 + 2839661 2839661 2839661 CACAATCTTGGCTTATTGCAGCCTCAATTCCTAGGCTTAAACAGTCCTCCCACCTCAGCCTCCTG CACAATCTTGGCTTATTGCAGCCTCAATTCCTGGGCTTAAACAGTCCTCCCACCTCAGCCTCCTG A G SH3BP2 Ensembl:ENSG00000087266 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1456926532 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89980,RMVar_hsa_circ_224397 20521 RMVar_ID_20521 Human_SNP_ID_170896374 A-to-I Human chr4 + 2839671 2839671 2839671 GCTTATTGCAGCCTCAATTCCTAGGCTTAAACAGTCCTCCCACCTCAGCCTCCTGAGTAGCCGGA GCTTATTGCAGCCTCAATTCCTAGGCTTAAACGGTCCTCCCACCTCAGCCTCCTGAGTAGCCGGA A G SH3BP2 Ensembl:ENSG00000087266 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs544003008 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89980,RMVar_hsa_circ_224397 20522 RMVar_ID_20522 Human_SNP_ID_170896384 A-to-I Human chr4 + 2839709 2839709 2839709 CCCACCTCAGCCTCCTGAGTAGCCGGAACTACAGTCACGCACTTCCATGTCCAGATAATTTTTTT CCCACCTCAGCCTCCTGAGTAGCCGGAACTACGGTCACGCACTTCCATGTCCAGATAATTTTTTT A G SH3BP2 Ensembl:ENSG00000087266 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs531267078 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_79 RMVar_hsa_circ_89980,RMVar_hsa_circ_224397 20523 RMVar_ID_20523 Human_SNP_ID_170896388 A-to-I Human chr4 + 2839729 2839729 2839729 AGCCGGAACTACAGTCACGCACTTCCATGTCCAGATAATTTTTTTTTTTTTTTTAGAGATAGGAT AGCCGGAACTACAGTCACGCACTTCCATGTCCGGATAATTTTTTTTTTTTTTTTAGAGATAGGAT A G SH3BP2 Ensembl:ENSG00000087266 Protein coding 3'UTR GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs1172258270 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89980,RMVar_hsa_circ_224397 20524 RMVar_ID_20524 Human_SNP_ID_170896408 A-to-I Human chr4 + 2839799 2839799 2839799 TATGCCCCAGCTGGTCTCAAACTCCTAGACTCAATGAGCCTCCCATCTTGACCTCCCAAAGTGCT TATGCCCCAGCTGGTCTCAAACTCCTAGACTCCATGAGCCTCCCATCTTGACCTCCCAAAGTGCT A C SH3BP2 Ensembl:ENSG00000087266 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs556190949 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17574705 Clinvar_Rec_80 RMVar_hsa_circ_89980,RMVar_hsa_circ_224397 20525 RMVar_ID_20525 Human_SNP_ID_170896416 A-to-I Human chr4 + 2839825 2839825 2839825 AGACTCAATGAGCCTCCCATCTTGACCTCCCAAAGTGCTGGGAGTACAGGCATGAGCCACTGTGC AGACTCAATGAGCCTCCCATCTTGACCTCCCAGAGTGCTGGGAGTACAGGCATGAGCCACTGTGC A G SH3BP2 Ensembl:ENSG00000087266 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs940840627 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89980,RMVar_hsa_circ_224397 20526 RMVar_ID_20526 Human_SNP_ID_170896446 A-to-I Human chr4 + 2839970 2839970 2839970 TTTCCAGGCTGGGTACAGTGGCTCACACCTGTAATGCCAGCACTTTGGGGGCAGAGGCAGGAGGA TTTCCAGGCTGGGTACAGTGGCTCACACCTGTCATGCCAGCACTTTGGGGGCAGAGGCAGGAGGA A C SH3BP2 Ensembl:ENSG00000087266 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs566113870 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17574597 Clinvar_Rec_81 RMVar_hsa_circ_89980,RMVar_hsa_circ_224397 20527 RMVar_ID_20527 Human_SNP_ID_170896467 A-to-I Human chr4 + 2840078 2840078 2840078 GAAACACCATCTCTACAAAAAATACAAAAATTAGCTGGACATGGTGGTGCGTGCCTGTAGTCCCA GAAACACCATCTCTACAAAAAATACAAAAATTGGCTGGACATGGTGGTGCGTGCCTGTAGTCCCA A G SH3BP2 Ensembl:ENSG00000087266 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,31158229,32596459 RNA-Seq:(High) rs1431247783 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17574707 RMVar_hsa_circ_89980,RMVar_hsa_circ_224397 20528 RMVar_ID_20528 Human_SNP_ID_170896475 A-to-I Human chr4 + 2840104 2840104 2840104 AAAATTAGCTGGACATGGTGGTGCGTGCCTGTAGTCCCAGCTACTCAGGTGGCTGGGGTGAGAGG AAAATTAGCTGGACATGGTGGTGCGTGCCTGTGGTCCCAGCTACTCAGGTGGCTGGGGTGAGAGG A G SH3BP2 Ensembl:ENSG00000087266 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1425352939 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17574707 RMVar_hsa_circ_89980,RMVar_hsa_circ_224397 20529 RMVar_ID_20529 Human_SNP_ID_170896477 A-to-I Human chr4 + 2840110 2840110 2840110 AGCTGGACATGGTGGTGCGTGCCTGTAGTCCCAGCTACTCAGGTGGCTGGGGTGAGAGGATTGCT AGCTGGACATGGTGGTGCGTGCCTGTAGTCCCGGCTACTCAGGTGGCTGGGGTGAGAGGATTGCT A G SH3BP2 Ensembl:ENSG00000087266 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs916364087 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17574707 RMVar_hsa_circ_89980,RMVar_hsa_circ_224397 20530 RMVar_ID_20530 Human_SNP_ID_170896478 A-to-I Human chr4 + 2840114 2840111 2840114 GGACATGGTGGTGCGTGCCTGTAGTCCCAGCTACTCAGGTGGCTGGGGTGAGAGGATTGCTTGAG GGACATGGTGGTGCGTGCCTGTAGTCCCAG___CTCAGGTGGCTGGGGTGAGAGGATTGCTTGAG GCTA G SH3BP2 Ensembl:ENSG00000087266 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1255485494 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_17574707 RMVar_hsa_circ_89980,RMVar_hsa_circ_224397 20531 RMVar_ID_20531 Human_SNP_ID_170896479 A-to-I Human chr4 + 2840114 2840114 2840114 GGACATGGTGGTGCGTGCCTGTAGTCCCAGCTACTCAGGTGGCTGGGGTGAGAGGATTGCTTGAG GGACATGGTGGTGCGTGCCTGTAGTCCCAGCTGCTCAGGTGGCTGGGGTGAGAGGATTGCTTGAG A G SH3BP2 Ensembl:ENSG00000087266 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1246626216 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17574707 RMVar_hsa_circ_89980,RMVar_hsa_circ_224397 20532 RMVar_ID_20532 Human_SNP_ID_170896481 A-to-I Human chr4 + 2840118 2840118 2840118 ATGGTGGTGCGTGCCTGTAGTCCCAGCTACTCAGGTGGCTGGGGTGAGAGGATTGCTTGAGCCCA ATGGTGGTGCGTGCCTGTAGTCCCAGCTACTCGGGTGGCTGGGGTGAGAGGATTGCTTGAGCCCA A G SH3BP2 Ensembl:ENSG00000087266 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1220090694 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17574707 RMVar_hsa_circ_89980,RMVar_hsa_circ_224397 20533 RMVar_ID_20533 Human_SNP_ID_170896487 A-to-I Human chr4 + 2840177 2840177 2840177 AGCCCAGAAGGTCAAGGCTGCAGTGAGCTGTGATTGTGCCACTGCACTTCAGCCTGTGAGACAGA AGCCCAGAAGGTCAAGGCTGCAGTGAGCTGTGGTTGTGCCACTGCACTTCAGCCTGTGAGACAGA A G SH3BP2 Ensembl:ENSG00000087266 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1275434299 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89980,RMVar_hsa_circ_224397 20534 RMVar_ID_20534 Human_SNP_ID_170896493 A-to-I Human chr4 + 2840220 2840220 2840220 GCACTTCAGCCTGTGAGACAGAGTGAGACCCTATCTCAAAAAAAACCAAAAAAAAAAAAAAAAAA GCACTTCAGCCTGTGAGACAGAGTGAGACCCTGTCTCAAAAAAAACCAAAAAAAAAAAAAAAAAA A G SH3BP2 Ensembl:ENSG00000087266 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1466811381 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89980,RMVar_hsa_circ_224397 20535 RMVar_ID_20535 Human_SNP_ID_170898035 A-to-I Human chr4 + 2845126 2845126 2845126 GACGGAGTCTCGCTCTGTCGCCAGGCTGGAGTACAGTGGCGCGATCTCCAGTCACTGCAATCTCC GACGGAGTCTCGCTCTGTCGCCAGGCTGGAGTGCAGTGGCGCGATCTCCAGTCACTGCAATCTCC A G ADD1 Ensembl:ENSG00000087274 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs540347749 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_224400,RMVar_hsa_circ_99003 20536 RMVar_ID_20536 Human_SNP_ID_170898056 A-to-I Human chr4 + 2845166 2845166 2845166 GCGATCTCCAGTCACTGCAATCTCCGCCTCCCAGGTTCAAGCAATTCTCCTACCTCAGCCTCCCG GCGATCTCCAGTCACTGCAATCTCCGCCTCCCGGGTTCAAGCAATTCTCCTACCTCAGCCTCCCG A G ADD1 Ensembl:ENSG00000087274 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1475799899 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_224400,RMVar_hsa_circ_99003 20537 RMVar_ID_20537 Human_SNP_ID_170898058 A-to-I Human chr4 + 2845176 2845176 2845176 GTCACTGCAATCTCCGCCTCCCAGGTTCAAGCAATTCTCCTACCTCAGCCTCCCGAGTAGCTGGG GTCACTGCAATCTCCGCCTCCCAGGTTCAAGCGATTCTCCTACCTCAGCCTCCCGAGTAGCTGGG A G ADD1 Ensembl:ENSG00000087274 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs370273641 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_224400,RMVar_hsa_circ_99003 20538 RMVar_ID_20538 Human_SNP_ID_170900846 A-to-I Human chr4 + 2854151 2854151 2854151 TGAGACCAGCTTGGCCGACATGGTGAAACCCCATCTGTACTAAAAATACAACAAAATTAGCCCAG TGAGACCAGCTTGGCCGACATGGTGAAACCCCCTCTGTACTAAAAATACAACAAAATTAGCCCAG A C ADD1 Ensembl:ENSG00000087274 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1226498023 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_224400,RMVar_hsa_circ_99003 20539 RMVar_ID_20539 Human_SNP_ID_170900847 A-to-I Human chr4 + 2854151 2854151 2854151 TGAGACCAGCTTGGCCGACATGGTGAAACCCCATCTGTACTAAAAATACAACAAAATTAGCCCAG TGAGACCAGCTTGGCCGACATGGTGAAACCCCTTCTGTACTAAAAATACAACAAAATTAGCCCAG A T ADD1 Ensembl:ENSG00000087274 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1226498023 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_224400,RMVar_hsa_circ_99003 20540 RMVar_ID_20540 Human_SNP_ID_170907213 A-to-I Human chr4 + 2879709 2879709 2879709 CAGTGGCGTGATCTCGGCTCACTGTAGCCTCCACCTCCCGAGTTCAAATGATTCTCCTGCCTCAG CAGTGGCGTGATCTCGGCTCACTGTAGCCTCCGCCTCCCGAGTTCAAATGATTCTCCTGCCTCAG A G ADD1 Ensembl:ENSG00000087274 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs953319666 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15137652 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_224404 20541 RMVar_ID_20541 Human_SNP_ID_170910377 A-to-I Human chr4 + 2890548 2890548 2890548 CCTGCCTCAACCTCCCGAGTAGCTGGGAGTACAGTCGCCCGCCACCACACCCGGCTAATTTTTTT CCTGCCTCAACCTCCCGAGTAGCTGGGAGTACGGTCGCCCGCCACCACACCCGGCTAATTTTTTT A G ADD1 Ensembl:ENSG00000087274 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1411075887 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73156,RMVar_hsa_circ_224400,RMVar_hsa_circ_99003,RMVar_hsa_circ_2986,RMVar_hsa_circ_62360,RMVar_hsa_circ_342711,RMVar_hsa_circ_351542,RMVar_hsa_circ_30215,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_52057,RMVar_hsa_circ_224406,RMVar_hsa_circ_224408,RMVar_hsa_circ_224407,RMVar_hsa_circ_224405,RMVar_hsa_circ_298270,RMVar_hsa_circ_224409 20542 RMVar_ID_20542 Human_SNP_ID_170913500 A-to-I Human chr4 + 2901955 2901955 2901955 TCTTTTTTTTTTTGGAGAGACAGGATGTCATCATGTTGCCTAGGCTGGTGTTGAACTCCTGGGCT TCTTTTTTTTTTTGGAGAGACAGGATGTCATCGTGTTGCCTAGGCTGGTGTTGAACTCCTGGGCT A G ADD1 Ensembl:ENSG00000087274 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs906977170 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_224400,RMVar_hsa_circ_99003,RMVar_hsa_circ_62360,RMVar_hsa_circ_351542,RMVar_hsa_circ_46430,RMVar_hsa_circ_327261,RMVar_hsa_circ_351600,RMVar_hsa_circ_224408,RMVar_hsa_circ_224407,RMVar_hsa_circ_111946,RMVar_hsa_circ_224410,RMVar_hsa_circ_360285,RMVar_hsa_circ_108212,RMVar_hsa_circ_224412,RMVar_hsa_circ_224413 20543 RMVar_ID_20543 Human_SNP_ID_170913517 A-to-I Human chr4 + 2902023 2902023 2902023 GCAGTCCTCCCACCTCAGCCTCCCAAAGTGCTAGGATTATGGGTGTAAACTACCACGCCTGACCC GCAGTCCTCCCACCTCAGCCTCCCAAAGTGCTGGGATTATGGGTGTAAACTACCACGCCTGACCC A G ADD1 Ensembl:ENSG00000087274 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1207455149 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_224400,RMVar_hsa_circ_99003,RMVar_hsa_circ_62360,RMVar_hsa_circ_351542,RMVar_hsa_circ_46430,RMVar_hsa_circ_327261,RMVar_hsa_circ_351600,RMVar_hsa_circ_224408,RMVar_hsa_circ_224407,RMVar_hsa_circ_111946,RMVar_hsa_circ_224410,RMVar_hsa_circ_360285,RMVar_hsa_circ_108212,RMVar_hsa_circ_224412,RMVar_hsa_circ_224413 20544 RMVar_ID_20544 Human_SNP_ID_170925109 A-to-I Human chr4 - 2938338 2938338 2938338 TTTTGTATTTTTAGTAGAGACGGGGTTTCTCCATGTTGGTCAGGCTGGTCTCGAATTCCCGACCT TTTTGTATTTTTAGTAGAGACGGGGTTTCTCCGTGTTGGTCAGGCTGGTCTCGAATTCCCGACCT T C NOP14 Ensembl:ENSG00000087269 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs534584680 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26518299 20545 RMVar_ID_20545 Human_SNP_ID_170925123 A-to-I Human chr4 - 2938358 2938358 2938358 GTGCCACCACGCCCAGCTAATTTTGTATTTTTAGTAGAGACGGGGTTTCTCCATGTTGGTCAGGC GTGCCACCACGCCCAGCTAATTTTGTATTTTTGGTAGAGACGGGGTTTCTCCATGTTGGTCAGGC T C NOP14 Ensembl:ENSG00000087269 Protein coding intron GSE38233;GSE99789;GSE112787;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;esophageal squamous carcinoma cells,EC109;293 Flip-In T-REx cells,empty vector;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29796672,29967493,32596459 RNA-Seq:(High) rs895833548 Functional Loss SNV dbSNP153 33..33 33 - - - 20546 RMVar_ID_20546 Human_SNP_ID_170925127 A-to-I Human chr4 - 2938364 2938364 2938364 AGACATGTGCCACCACGCCCAGCTAATTTTGTATTTTTAGTAGAGACGGGGTTTCTCCATGTTGG AGACATGTGCCACCACGCCCAGCTAATTTTGTTTTTTTAGTAGAGACGGGGTTTCTCCATGTTGG T A NOP14 Ensembl:ENSG00000087269 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1458439094 Functional Loss SNV dbSNP153 33..33 33 - - - 20547 RMVar_ID_20547 Human_SNP_ID_170925132 A-to-I Human chr4 - 2938371 2938371 2938371 GGATTACAGACATGTGCCACCACGCCCAGCTAATTTTGTATTTTTAGTAGAGACGGGGTTTCTCC GGATTACAGACATGTGCCACCACGCCCAGCTAGTTTTGTATTTTTAGTAGAGACGGGGTTTCTCC T C NOP14 Ensembl:ENSG00000087269 Protein coding intron GSE38233;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,32596459 RNA-Seq:(High) rs921939090 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_162032 20548 RMVar_ID_20548 Human_SNP_ID_170925191 A-to-I Human chr4 - 2938465 2938465 2938465 AGTTTTGCTCTTGTTGCCCAGGCTGGAGTGCAATGGCACAACCTCCACCTCCTGGGTTCAAGCGA AGTTTTGCTCTTGTTGCCCAGGCTGGAGTGCAGTGGCACAACCTCCACCTCCTGGGTTCAAGCGA T C NOP14 Ensembl:ENSG00000087269 Protein coding intron GSE38233;GSE100210;GSE112787 cultured B-cells;HepG2 cell line;293 Flip-In T-REx cells,empty vector - 24183664,29129909,29967493 RNA-Seq:(High) rs550802521 Functional Loss SNV dbSNP153 33..33 33 - - - 20549 RMVar_ID_20549 Human_SNP_ID_170925271 A-to-I Human chr4 - 2938637 2938637 2938637 GCCAAGTGTGGTGGCACGCACCTGTAGTCCCAACTACTCGGGAGGCTGAAGCAGGAGGACTGCTT GCCAAGTGTGGTGGCACGCACCTGTAGTCCCAGCTACTCGGGAGGCTGAAGCAGGAGGACTGCTT T C NOP14 Ensembl:ENSG00000087269 Protein coding intron GSE38233;GSE100210;GSE112787;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;293 Flip-In T-REx cells,empty vector;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,29967493,32596459,32596459 RNA-Seq:(High) rs566394158 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26515179 20550 RMVar_ID_20550 Human_SNP_ID_170925277 A-to-I Human chr4 - 2938644 2938644 2938644 AAAATTAGCCAAGTGTGGTGGCACGCACCTGTAGTCCCAACTACTCGGGAGGCTGAAGCAGGAGG AAAATTAGCCAAGTGTGGTGGCACGCACCTGTGGTCCCAACTACTCGGGAGGCTGAAGCAGGAGG T C NOP14 Ensembl:ENSG00000087269 Protein coding intron GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490829,GSM3490830,GSM3490831 HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,EC109 cell line - 29129909,29796672,31158229,31158229,32596459 RNA-Seq:(High) rs1357965368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26515180 Human_miRNA_ID_276826 20551 RMVar_ID_20551 Human_SNP_ID_170925305 A-to-I Human chr4 - 2938670 2938670 2938670 GACCCCGTCTCTACCAAAAAAACATAAAAATTAGCCAAGTGTGGTGGCACGCACCTGTAGTCCCA GACCCCGTCTCTACCAAAAAAACATAAAAATTGGCCAAGTGTGGTGGCACGCACCTGTAGTCCCA T C NOP14 Ensembl:ENSG00000087269 Protein coding intron GSE38233;GSE100210;GSE99789;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,29796672,32596459 RNA-Seq:(High) rs1315525395 Functional Loss SNV dbSNP153 33..33 33 - - - 20552 RMVar_ID_20552 Human_SNP_ID_170925327 A-to-I Human chr4 - 2938735 2938735 2938735 GGGAGGCCAAGGCAGGAAGATTGCTTCAGCCCAGGAGTTCGAGACCAGCCTGGGCAACACAGGAA GGGAGGCCAAGGCAGGAAGATTGCTTCAGCCCGGGAGTTCGAGACCAGCCTGGGCAACACAGGAA T C NOP14 Ensembl:ENSG00000087269 Protein coding intron GSE38233;GSE100210;GSE99789;GSE112787;GSE107867;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;293 Flip-In T-REx cells,empty vector;ASD brains,cerebellum;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,29796672,29967493,30559470,32596459,32596459 RNA-Seq:(High) rs1456204463 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4799170,Human_RBP_ID_22291194,Human_RBP_ID_22826081,Human_RBP_ID_25806236,Human_RBP_ID_27067431 20553 RMVar_ID_20553 Human_SNP_ID_170925333 A-to-I Human chr4 - 2938759 2938759 2938759 TCACATCTGCAATTCCAACCCTCTGGGAGGCCAAGGCAGGAAGATTGCTTCAGCCCAGGAGTTCG TCACATCTGCAATTCCAACCCTCTGGGAGGCCGAGGCAGGAAGATTGCTTCAGCCCAGGAGTTCG T C NOP14 Ensembl:ENSG00000087269 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232820290 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18025057,Human_RBP_ID_22826081 20554 RMVar_ID_20554 Human_SNP_ID_170931867 A-to-I Human chr4 - 2959350 2959350 2959350 CTAACCTCGTGATCCGCCCGCCTTGGCCTCCCAGAGTGCTGGAATTACAGGCGTGAGCCACCGCG CTAACCTCGTGATCCGCCCGCCTTGGCCTCCCTGAGTGCTGGAATTACAGGCGTGAGCCACCGCG T A NOP14 Ensembl:ENSG00000087269 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs532861665 Functional Loss SNV dbSNP153 33..33 33 - - - 20555 RMVar_ID_20555 Human_SNP_ID_170931868 A-to-I Human chr4 - 2959350 2959350 2959350 CTAACCTCGTGATCCGCCCGCCTTGGCCTCCCAGAGTGCTGGAATTACAGGCGTGAGCCACCGCG CTAACCTCGTGATCCGCCCGCCTTGGCCTCCCGGAGTGCTGGAATTACAGGCGTGAGCCACCGCG T C NOP14 Ensembl:ENSG00000087269 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs532861665 Functional Loss SNV dbSNP153 33..33 33 - - - 20556 RMVar_ID_20556 Human_SNP_ID_170934926 A-to-I Human chr4 + 2966140 2966140 2966140 GATAGTTTGAAAAATGAAAGTTTTGGCCGGGCACGGTGGCTCACAGCTGTAATCCCAGCACTTTT GATAGTTTGAAAAATGAAAGTTTTGGCCGGGCCCGGTGGCTCACAGCTGTAATCCCAGCACTTTT A C GRK4 Ensembl:ENSG00000125388 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs539172730 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24052842 20557 RMVar_ID_20557 Human_SNP_ID_170934927 A-to-I Human chr4 + 2966140 2966140 2966140 GATAGTTTGAAAAATGAAAGTTTTGGCCGGGCACGGTGGCTCACAGCTGTAATCCCAGCACTTTT GATAGTTTGAAAAATGAAAGTTTTGGCCGGGCGCGGTGGCTCACAGCTGTAATCCCAGCACTTTT A G GRK4 Ensembl:ENSG00000125388 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs539172730 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24052842 20558 RMVar_ID_20558 Human_SNP_ID_170934931 A-to-I Human chr4 + 2966152 2966152 2966152 AATGAAAGTTTTGGCCGGGCACGGTGGCTCACAGCTGTAATCCCAGCACTTTTGGAGGCCGAGGC AATGAAAGTTTTGGCCGGGCACGGTGGCTCACGGCTGTAATCCCAGCACTTTTGGAGGCCGAGGC A G GRK4 Ensembl:ENSG00000125388 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs576027479 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24052842 20559 RMVar_ID_20559 Human_SNP_ID_170935447 A-to-I Human chr4 + 2967956 2967956 2967956 GGGATTACAGGCATGCACCATTATGCCTGGCTAATTTTGTATTTTTAGTAGAGACGGGGGTTTCT GGGATTACAGGCATGCACCATTATGCCTGGCTGATTTTGTATTTTTAGTAGAGACGGGGGTTTCT A G GRK4 Ensembl:ENSG00000125388 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1481773699 Functional Loss SNV dbSNP153 33..33 33 - - - 20560 RMVar_ID_20560 Human_SNP_ID_170935450 A-to-I Human chr4 + 2967964 2967964 2967964 AGGCATGCACCATTATGCCTGGCTAATTTTGTATTTTTAGTAGAGACGGGGGTTTCTCCATGTTG AGGCATGCACCATTATGCCTGGCTAATTTTGTGTTTTTAGTAGAGACGGGGGTTTCTCCATGTTG A G GRK4 Ensembl:ENSG00000125388 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs981566365 Functional Loss SNV dbSNP153 33..33 33 - - - 20561 RMVar_ID_20561 Human_SNP_ID_170935954 A-to-I Human chr4 + 2969934 2969934 2969934 CCTGGACTCAAGTGATCCTACCCTCCCACTTCAGCCTCCCAAAGTGCTGGGATTACAGGGTGAAC CCTGGACTCAAGTGATCCTACCCTCCCACTTCTGCCTCCCAAAGTGCTGGGATTACAGGGTGAAC A T GRK4 Ensembl:ENSG00000125388 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1347829727 Functional Loss SNV dbSNP153 33..33 33 - - - 20562 RMVar_ID_20562 Human_SNP_ID_170936086 A-to-I Human chr4 + 2970502 2970502 2970502 CAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCCAGGCATGGTGGCATGCACCT CAACATGGTGAAACCCCGTCTCTACTAAAAATGCAAAAATTAGCCAGGCATGGTGGCATGCACCT A G GRK4 Ensembl:ENSG00000125388 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs576539066 Functional Loss SNV dbSNP153 33..33 33 - - - 20563 RMVar_ID_20563 Human_SNP_ID_170936122 A-to-I Human chr4 + 2970623 2970623 2970623 GAGGTTGCAGTGAGCCGAGATCGTGCCACTGCACTCCAACCTGGCGACACGGTGAGACTCCATCT GAGGTTGCAGTGAGCCGAGATCGTGCCACTGCCCTCCAACCTGGCGACACGGTGAGACTCCATCT A C GRK4 Ensembl:ENSG00000125388 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs899576784 Functional Loss SNV dbSNP153 33..33 33 - - - 20564 RMVar_ID_20564 Human_SNP_ID_170936194 A-to-I Human chr4 + 2970811 2970811 2970811 CCTGTCTCAGCCTCCCCAGCAGCTGGGACTACAGGCACACGCCGCCATGCCTGGCTAATTTTTTT CCTGTCTCAGCCTCCCCAGCAGCTGGGACTACGGGCACACGCCGCCATGCCTGGCTAATTTTTTT A G GRK4 Ensembl:ENSG00000125388 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1358595246 Functional Loss SNV dbSNP153 33..33 33 - - - 20565 RMVar_ID_20565 Human_SNP_ID_170971730 A-to-I Human chr4 + 3104389 3104389 3104389 CCCAGCATTTTGGGAGGCTGAGGCAGGTGATCACCTGAGATCAGGAGTTCGAGACCAGCCTGGCC CCCAGCATTTTGGGAGGCTGAGGCAGGTGATCTCCTGAGATCAGGAGTTCGAGACCAGCCTGGCC A T HTT Ensembl:ENSG00000197386 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1262385458 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104639,RMVar_hsa_circ_103876,RMVar_hsa_circ_295563,RMVar_hsa_circ_329840,RMVar_hsa_circ_348118,RMVar_hsa_circ_360715,RMVar_hsa_circ_224463,RMVar_hsa_circ_371790,RMVar_hsa_circ_358944,RMVar_hsa_circ_341125,RMVar_hsa_circ_348113,RMVar_hsa_circ_333631,RMVar_hsa_circ_316973,RMVar_hsa_circ_308507,RMVar_hsa_circ_122246,RMVar_hsa_circ_276360,RMVar_hsa_circ_276005,RMVar_hsa_circ_112489,RMVar_hsa_circ_121251,RMVar_hsa_circ_111934,RMVar_hsa_circ_1511,RMVar_hsa_circ_224468,RMVar_hsa_circ_64469,RMVar_hsa_circ_74550,RMVar_hsa_circ_47136,RMVar_hsa_circ_224472,RMVar_hsa_circ_24019,RMVar_hsa_circ_26831,RMVar_hsa_circ_224474,RMVar_hsa_circ_19523,RMVar_hsa_circ_224473,RMVar_hsa_circ_224470,RMVar_hsa_circ_224471,RMVar_hsa_circ_224469,RMVar_hsa_circ_224464,RMVar_hsa_circ_224466,RMVar_hsa_circ_224467,RMVar_hsa_circ_224465,RMVar_hsa_circ_309822,RMVar_hsa_circ_224476,RMVar_hsa_circ_280261,RMVar_hsa_circ_336363,RMVar_hsa_circ_378954,RMVar_hsa_circ_328423,RMVar_hsa_circ_102826,RMVar_hsa_circ_118673,RMVar_hsa_circ_62404,RMVar_hsa_circ_224478,RMVar_hsa_circ_224479,RMVar_hsa_circ_224477 20566 RMVar_ID_20566 Human_SNP_ID_170980831 A-to-I Human chr4 + 3140096 3140096 3140096 CAGCCTGGCCAAGGTGATGAAACCCTGTCTCTACTAAAACTACAAAAATTAGCCGGGCGCGGTGG CAGCCTGGCCAAGGTGATGAAACCCTGTCTCTCCTAAAACTACAAAAATTAGCCGGGCGCGGTGG A C HTT Ensembl:ENSG00000197386 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs745621328 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2649,RMVar_hsa_circ_104639,RMVar_hsa_circ_329840,RMVar_hsa_circ_348113,RMVar_hsa_circ_333631,RMVar_hsa_circ_122246,RMVar_hsa_circ_112489,RMVar_hsa_circ_121251,RMVar_hsa_circ_111934,RMVar_hsa_circ_224468,RMVar_hsa_circ_64469,RMVar_hsa_circ_74550,RMVar_hsa_circ_24019,RMVar_hsa_circ_19523,RMVar_hsa_circ_224464,RMVar_hsa_circ_224466,RMVar_hsa_circ_224467,RMVar_hsa_circ_224465,RMVar_hsa_circ_102826,RMVar_hsa_circ_31104,RMVar_hsa_circ_85123,RMVar_hsa_circ_127381,RMVar_hsa_circ_224479,RMVar_hsa_circ_224481,RMVar_hsa_circ_224480,RMVar_hsa_circ_85650,RMVar_hsa_circ_86034,RMVar_hsa_circ_124284,RMVar_hsa_circ_224487,RMVar_hsa_circ_224489,RMVar_hsa_circ_224490,RMVar_hsa_circ_57382,RMVar_hsa_circ_101101,RMVar_hsa_circ_47821,RMVar_hsa_circ_224495,RMVar_hsa_circ_102920,RMVar_hsa_circ_224494,RMVar_hsa_circ_106056,RMVar_hsa_circ_224497,RMVar_hsa_circ_88372,RMVar_hsa_circ_224498,RMVar_hsa_circ_224496,RMVar_hsa_circ_96024,RMVar_hsa_circ_359477,RMVar_hsa_circ_331876,RMVar_hsa_circ_3756,RMVar_hsa_circ_30680,RMVar_hsa_circ_224501,RMVar_hsa_circ_364823,RMVar_hsa_circ_41444,RMVar_hsa_circ_116336,RMVar_hsa_circ_224505,RMVar_hsa_circ_110586,RMVar_hsa_circ_126154,RMVar_hsa_circ_224506,RMVar_hsa_circ_33882,RMVar_hsa_circ_224509,RMVar_hsa_circ_114515,RMVar_hsa_circ_224507,RMVar_hsa_circ_89392,RMVar_hsa_circ_224510,RMVar_hsa_circ_41420,RMVar_hsa_circ_108449,RMVar_hsa_circ_123480,RMVar_hsa_circ_66401,RMVar_hsa_circ_100165,RMVar_hsa_circ_123958,RMVar_hsa_circ_224512,RMVar_hsa_circ_224511,RMVar_hsa_circ_101455,RMVar_hsa_circ_224514,RMVar_hsa_circ_15125,RMVar_hsa_circ_22092,RMVar_hsa_circ_224515,RMVar_hsa_circ_224516 20567 RMVar_ID_20567 Human_SNP_ID_170980849 A-to-I Human chr4 + 3140140 3140140 3140140 AAAATTAGCCGGGCGCGGTGGCAGGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA AAAATTAGCCGGGCGCGGTGGCAGGCGCCTGTTATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA A T HTT Ensembl:ENSG00000197386 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs963699057 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2649,RMVar_hsa_circ_104639,RMVar_hsa_circ_329840,RMVar_hsa_circ_348113,RMVar_hsa_circ_333631,RMVar_hsa_circ_122246,RMVar_hsa_circ_112489,RMVar_hsa_circ_121251,RMVar_hsa_circ_111934,RMVar_hsa_circ_224468,RMVar_hsa_circ_64469,RMVar_hsa_circ_74550,RMVar_hsa_circ_24019,RMVar_hsa_circ_19523,RMVar_hsa_circ_224464,RMVar_hsa_circ_224466,RMVar_hsa_circ_224467,RMVar_hsa_circ_224465,RMVar_hsa_circ_102826,RMVar_hsa_circ_31104,RMVar_hsa_circ_85123,RMVar_hsa_circ_127381,RMVar_hsa_circ_224479,RMVar_hsa_circ_224481,RMVar_hsa_circ_224480,RMVar_hsa_circ_85650,RMVar_hsa_circ_86034,RMVar_hsa_circ_124284,RMVar_hsa_circ_224487,RMVar_hsa_circ_224489,RMVar_hsa_circ_224490,RMVar_hsa_circ_57382,RMVar_hsa_circ_101101,RMVar_hsa_circ_47821,RMVar_hsa_circ_224495,RMVar_hsa_circ_102920,RMVar_hsa_circ_224494,RMVar_hsa_circ_106056,RMVar_hsa_circ_224497,RMVar_hsa_circ_88372,RMVar_hsa_circ_224498,RMVar_hsa_circ_224496,RMVar_hsa_circ_96024,RMVar_hsa_circ_359477,RMVar_hsa_circ_331876,RMVar_hsa_circ_3756,RMVar_hsa_circ_30680,RMVar_hsa_circ_224501,RMVar_hsa_circ_364823,RMVar_hsa_circ_41444,RMVar_hsa_circ_116336,RMVar_hsa_circ_224505,RMVar_hsa_circ_110586,RMVar_hsa_circ_126154,RMVar_hsa_circ_224506,RMVar_hsa_circ_33882,RMVar_hsa_circ_224509,RMVar_hsa_circ_114515,RMVar_hsa_circ_224507,RMVar_hsa_circ_89392,RMVar_hsa_circ_224510,RMVar_hsa_circ_41420,RMVar_hsa_circ_108449,RMVar_hsa_circ_123480,RMVar_hsa_circ_66401,RMVar_hsa_circ_100165,RMVar_hsa_circ_123958,RMVar_hsa_circ_224512,RMVar_hsa_circ_224511,RMVar_hsa_circ_101455,RMVar_hsa_circ_224514,RMVar_hsa_circ_15125,RMVar_hsa_circ_22092,RMVar_hsa_circ_224515,RMVar_hsa_circ_224516 20568 RMVar_ID_20568 Human_SNP_ID_170981679 A-to-I Human chr4 + 3143227 3143227 3143227 GGGAGGCCAAGGTTGGGGGCTCACTTGAGGTCAGGAGTCGGATACCAGCCTGGCCAACGTGGTGA GGGAGGCCAAGGTTGGGGGCTCACTTGAGGTCGGGAGTCGGATACCAGCCTGGCCAACGTGGTGA A G HTT Ensembl:ENSG00000197386 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs983581237 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104639,RMVar_hsa_circ_329840,RMVar_hsa_circ_348113,RMVar_hsa_circ_333631,RMVar_hsa_circ_122246,RMVar_hsa_circ_112489,RMVar_hsa_circ_121251,RMVar_hsa_circ_111934,RMVar_hsa_circ_224468,RMVar_hsa_circ_64469,RMVar_hsa_circ_74550,RMVar_hsa_circ_24019,RMVar_hsa_circ_19523,RMVar_hsa_circ_224464,RMVar_hsa_circ_224466,RMVar_hsa_circ_224467,RMVar_hsa_circ_224465,RMVar_hsa_circ_102826,RMVar_hsa_circ_31104,RMVar_hsa_circ_85123,RMVar_hsa_circ_127381,RMVar_hsa_circ_224479,RMVar_hsa_circ_224481,RMVar_hsa_circ_224480,RMVar_hsa_circ_85650,RMVar_hsa_circ_86034,RMVar_hsa_circ_124284,RMVar_hsa_circ_224487,RMVar_hsa_circ_224489,RMVar_hsa_circ_224490,RMVar_hsa_circ_57382,RMVar_hsa_circ_101101,RMVar_hsa_circ_47821,RMVar_hsa_circ_224495,RMVar_hsa_circ_102920,RMVar_hsa_circ_224494,RMVar_hsa_circ_106056,RMVar_hsa_circ_224497,RMVar_hsa_circ_88372,RMVar_hsa_circ_224498,RMVar_hsa_circ_224496,RMVar_hsa_circ_96024,RMVar_hsa_circ_331876,RMVar_hsa_circ_3756,RMVar_hsa_circ_30680,RMVar_hsa_circ_224501,RMVar_hsa_circ_41444,RMVar_hsa_circ_116336,RMVar_hsa_circ_224505,RMVar_hsa_circ_110586,RMVar_hsa_circ_126154,RMVar_hsa_circ_224506,RMVar_hsa_circ_33882,RMVar_hsa_circ_224509,RMVar_hsa_circ_114515,RMVar_hsa_circ_224507,RMVar_hsa_circ_89392,RMVar_hsa_circ_224510,RMVar_hsa_circ_41420,RMVar_hsa_circ_108449,RMVar_hsa_circ_123480,RMVar_hsa_circ_32731,RMVar_hsa_circ_100165,RMVar_hsa_circ_123958,RMVar_hsa_circ_224512,RMVar_hsa_circ_224511,RMVar_hsa_circ_101455,RMVar_hsa_circ_224514,RMVar_hsa_circ_224515,RMVar_hsa_circ_224516,RMVar_hsa_circ_61886,RMVar_hsa_circ_111907,RMVar_hsa_circ_34654,RMVar_hsa_circ_19458,RMVar_hsa_circ_59741,RMVar_hsa_circ_224517,RMVar_hsa_circ_374108,RMVar_hsa_circ_35920,RMVar_hsa_circ_224518 20569 RMVar_ID_20569 Human_SNP_ID_170984074 A-to-I Human chr4 + 3152057 3152057 3152057 TCAAGTGATCCTTCTGCCTCAGCCTTCTCAGTAGTTGGGACTACAGGCATACCCACCATGCCCAG TCAAGTGATCCTTCTGCCTCAGCCTTCTCAGTGGTTGGGACTACAGGCATACCCACCATGCCCAG A G HTT Ensembl:ENSG00000197386 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs901700976 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104639,RMVar_hsa_circ_329840,RMVar_hsa_circ_348113,RMVar_hsa_circ_333631,RMVar_hsa_circ_122246,RMVar_hsa_circ_112489,RMVar_hsa_circ_121251,RMVar_hsa_circ_64469,RMVar_hsa_circ_24019,RMVar_hsa_circ_19523,RMVar_hsa_circ_224464,RMVar_hsa_circ_224466,RMVar_hsa_circ_224467,RMVar_hsa_circ_224465,RMVar_hsa_circ_102826,RMVar_hsa_circ_85123,RMVar_hsa_circ_127381,RMVar_hsa_circ_224479,RMVar_hsa_circ_224481,RMVar_hsa_circ_224480,RMVar_hsa_circ_85650,RMVar_hsa_circ_86034,RMVar_hsa_circ_124284,RMVar_hsa_circ_224487,RMVar_hsa_circ_224489,RMVar_hsa_circ_224490,RMVar_hsa_circ_57382,RMVar_hsa_circ_101101,RMVar_hsa_circ_224495,RMVar_hsa_circ_102920,RMVar_hsa_circ_224494,RMVar_hsa_circ_106056,RMVar_hsa_circ_224497,RMVar_hsa_circ_88372,RMVar_hsa_circ_224498,RMVar_hsa_circ_224496,RMVar_hsa_circ_96024,RMVar_hsa_circ_331876,RMVar_hsa_circ_3756,RMVar_hsa_circ_224501,RMVar_hsa_circ_41444,RMVar_hsa_circ_116336,RMVar_hsa_circ_224505,RMVar_hsa_circ_110586,RMVar_hsa_circ_114515,RMVar_hsa_circ_224507,RMVar_hsa_circ_224510,RMVar_hsa_circ_41420,RMVar_hsa_circ_108449,RMVar_hsa_circ_6884,RMVar_hsa_circ_32731,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_34654,RMVar_hsa_circ_19458,RMVar_hsa_circ_59741,RMVar_hsa_circ_224517,RMVar_hsa_circ_374108,RMVar_hsa_circ_35920,RMVar_hsa_circ_12378,RMVar_hsa_circ_224518,RMVar_hsa_circ_363235,RMVar_hsa_circ_106414,RMVar_hsa_circ_76196,RMVar_hsa_circ_224519,RMVar_hsa_circ_343160,RMVar_hsa_circ_224520 20570 RMVar_ID_20570 Human_SNP_ID_170984157 A-to-I Human chr4 + 3152372 3152372 3152372 AGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCTACCGCTCCCAGCCAGGAAAC AGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTGCAGGCGTGAGCTACCGCTCCCAGCCAGGAAAC A G HTT Ensembl:ENSG00000197386 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1470387964 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104639,RMVar_hsa_circ_329840,RMVar_hsa_circ_348113,RMVar_hsa_circ_333631,RMVar_hsa_circ_122246,RMVar_hsa_circ_112489,RMVar_hsa_circ_121251,RMVar_hsa_circ_64469,RMVar_hsa_circ_24019,RMVar_hsa_circ_19523,RMVar_hsa_circ_224464,RMVar_hsa_circ_224466,RMVar_hsa_circ_224467,RMVar_hsa_circ_224465,RMVar_hsa_circ_102826,RMVar_hsa_circ_85123,RMVar_hsa_circ_127381,RMVar_hsa_circ_224479,RMVar_hsa_circ_224481,RMVar_hsa_circ_224480,RMVar_hsa_circ_85650,RMVar_hsa_circ_86034,RMVar_hsa_circ_124284,RMVar_hsa_circ_224487,RMVar_hsa_circ_224489,RMVar_hsa_circ_224490,RMVar_hsa_circ_57382,RMVar_hsa_circ_101101,RMVar_hsa_circ_224495,RMVar_hsa_circ_102920,RMVar_hsa_circ_224494,RMVar_hsa_circ_106056,RMVar_hsa_circ_224497,RMVar_hsa_circ_88372,RMVar_hsa_circ_224498,RMVar_hsa_circ_224496,RMVar_hsa_circ_96024,RMVar_hsa_circ_331876,RMVar_hsa_circ_3756,RMVar_hsa_circ_224501,RMVar_hsa_circ_41444,RMVar_hsa_circ_116336,RMVar_hsa_circ_224505,RMVar_hsa_circ_110586,RMVar_hsa_circ_114515,RMVar_hsa_circ_224507,RMVar_hsa_circ_224510,RMVar_hsa_circ_41420,RMVar_hsa_circ_108449,RMVar_hsa_circ_6884,RMVar_hsa_circ_32731,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_34654,RMVar_hsa_circ_19458,RMVar_hsa_circ_59741,RMVar_hsa_circ_224517,RMVar_hsa_circ_374108,RMVar_hsa_circ_35920,RMVar_hsa_circ_12378,RMVar_hsa_circ_224518,RMVar_hsa_circ_363235,RMVar_hsa_circ_106414,RMVar_hsa_circ_76196,RMVar_hsa_circ_224519,RMVar_hsa_circ_343160,RMVar_hsa_circ_224520 20571 RMVar_ID_20571 Human_SNP_ID_170985203 A-to-I Human chr4 + 3156173 3156173 3156173 TGAGATGGAGTCTTCTTCACCCAGGCTGGAGTACCATGGCACGATCTCATCTCACTGCAACCTCC TGAGATGGAGTCTTCTTCACCCAGGCTGGAGTGCCATGGCACGATCTCATCTCACTGCAACCTCC A G HTT Ensembl:ENSG00000197386 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1359036179 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104639,RMVar_hsa_circ_329840,RMVar_hsa_circ_348113,RMVar_hsa_circ_333631,RMVar_hsa_circ_122246,RMVar_hsa_circ_112489,RMVar_hsa_circ_121251,RMVar_hsa_circ_64469,RMVar_hsa_circ_24019,RMVar_hsa_circ_224464,RMVar_hsa_circ_224466,RMVar_hsa_circ_224467,RMVar_hsa_circ_224465,RMVar_hsa_circ_102826,RMVar_hsa_circ_85123,RMVar_hsa_circ_127381,RMVar_hsa_circ_224479,RMVar_hsa_circ_224481,RMVar_hsa_circ_224480,RMVar_hsa_circ_85650,RMVar_hsa_circ_86034,RMVar_hsa_circ_124284,RMVar_hsa_circ_224487,RMVar_hsa_circ_224489,RMVar_hsa_circ_224490,RMVar_hsa_circ_101101,RMVar_hsa_circ_224495,RMVar_hsa_circ_102920,RMVar_hsa_circ_224494,RMVar_hsa_circ_106056,RMVar_hsa_circ_224497,RMVar_hsa_circ_88372,RMVar_hsa_circ_224498,RMVar_hsa_circ_224496,RMVar_hsa_circ_96024,RMVar_hsa_circ_331876,RMVar_hsa_circ_3756,RMVar_hsa_circ_224501,RMVar_hsa_circ_41444,RMVar_hsa_circ_116336,RMVar_hsa_circ_224505,RMVar_hsa_circ_110586,RMVar_hsa_circ_114515,RMVar_hsa_circ_224507,RMVar_hsa_circ_224510,RMVar_hsa_circ_41420,RMVar_hsa_circ_108449,RMVar_hsa_circ_6884,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_34654,RMVar_hsa_circ_19458,RMVar_hsa_circ_224517,RMVar_hsa_circ_374108,RMVar_hsa_circ_35920,RMVar_hsa_circ_12378,RMVar_hsa_circ_224518,RMVar_hsa_circ_363235,RMVar_hsa_circ_106414,RMVar_hsa_circ_52143,RMVar_hsa_circ_76196,RMVar_hsa_circ_224519,RMVar_hsa_circ_283295,RMVar_hsa_circ_224520,RMVar_hsa_circ_274844,RMVar_hsa_circ_224521,RMVar_hsa_circ_224522 20572 RMVar_ID_20572 Human_SNP_ID_170994104 A-to-I Human chr4 + 3190174 3190174 3190174 GGGACCAGCCTGAGCAACATATCGAGACCCCTATCTCTACAAAGAAAATCAAAAACTAGCTAGAT GGGACCAGCCTGAGCAACATATCGAGACCCCTGTCTCTACAAAGAAAATCAAAAACTAGCTAGAT A G HTT Ensembl:ENSG00000197386 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs966023963 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122246,RMVar_hsa_circ_112489,RMVar_hsa_circ_224464,RMVar_hsa_circ_224465,RMVar_hsa_circ_85123,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_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_52143,RMVar_hsa_circ_224519,RMVar_hsa_circ_224524,RMVar_hsa_circ_303354,RMVar_hsa_circ_81408,RMVar_hsa_circ_104227,RMVar_hsa_circ_224525,RMVar_hsa_circ_122033,RMVar_hsa_circ_224530,RMVar_hsa_circ_224527,RMVar_hsa_circ_326150,RMVar_hsa_circ_276279,RMVar_hsa_circ_224529,RMVar_hsa_circ_271039,RMVar_hsa_circ_317450,RMVar_hsa_circ_128182,RMVar_hsa_circ_224534,RMVar_hsa_circ_92121,RMVar_hsa_circ_224535,RMVar_hsa_circ_224532,RMVar_hsa_circ_224533,RMVar_hsa_circ_224531,RMVar_hsa_circ_224538,RMVar_hsa_circ_75915 20573 RMVar_ID_20573 Human_SNP_ID_170994105 A-to-I Human chr4 + 3190174 3190174 3190174 GGGACCAGCCTGAGCAACATATCGAGACCCCTATCTCTACAAAGAAAATCAAAAACTAGCTAGAT GGGACCAGCCTGAGCAACATATCGAGACCCCTTTCTCTACAAAGAAAATCAAAAACTAGCTAGAT A T HTT Ensembl:ENSG00000197386 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs966023963 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122246,RMVar_hsa_circ_112489,RMVar_hsa_circ_224464,RMVar_hsa_circ_224465,RMVar_hsa_circ_85123,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_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_52143,RMVar_hsa_circ_224519,RMVar_hsa_circ_224524,RMVar_hsa_circ_303354,RMVar_hsa_circ_81408,RMVar_hsa_circ_104227,RMVar_hsa_circ_224525,RMVar_hsa_circ_122033,RMVar_hsa_circ_224530,RMVar_hsa_circ_224527,RMVar_hsa_circ_326150,RMVar_hsa_circ_276279,RMVar_hsa_circ_224529,RMVar_hsa_circ_271039,RMVar_hsa_circ_317450,RMVar_hsa_circ_128182,RMVar_hsa_circ_224534,RMVar_hsa_circ_92121,RMVar_hsa_circ_224535,RMVar_hsa_circ_224532,RMVar_hsa_circ_224533,RMVar_hsa_circ_224531,RMVar_hsa_circ_224538,RMVar_hsa_circ_75915 20574 RMVar_ID_20574 Human_SNP_ID_171077963 A-to-I Human chr4 - 3481061 3481061 3481061 CCCAACAGGGCTCCTACACAGCCCTTCGGGACACCCATTCGTGCTCAAAGATGTCTGAAGTGCCC CCCAACAGGGCTCCTACACAGCCCTTCGGGACGCCCATTCGTGCTCAAAGATGTCTGAAGTGCCC T C lnc-LRPAP1-4 RNACentral:URS00008C0148 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1457245994 Functional Loss SNV dbSNP153 33..33 33 - - - 20575 RMVar_ID_20575 Human_SNP_ID_171078300 A-to-I Human chr4 - 3482099 3482099 3482099 TTTGAGCACAAACGGGTGTCCCAAAGGGCTGTATAGGAGCCCTGTTGTGGGGGATAGGAGGCGTG TTTGAGCACAAACGGGTGTCCCAAAGGGCTGTGTAGGAGCCCTGTTGTGGGGGATAGGAGGCGTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs137988150 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2845088 20576 RMVar_ID_20576 Human_SNP_ID_171078302 A-to-I Human chr4 - 3482109 3482109 3482109 GTCAGACATCTTTGAGCACAAACGGGTGTCCCAAAGGGCTGTATAGGAGCCCTGTTGTGGGGGAT GTCAGACATCTTTGAGCACAAACGGGTGTCCCGAAGGGCTGTATAGGAGCCCTGTTGTGGGGGAT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1461511920 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2845088 20577 RMVar_ID_20577 Human_SNP_ID_171078306 A-to-I Human chr4 - 3482122 3482122 3482122 GTGAAAAGGGCACGTCAGACATCTTTGAGCACAAACGGGTGTCCCAAAGGGCTGTATAGGAGCCC GTGAAAAGGGCACGTCAGACATCTTTGAGCACGAACGGGTGTCCCAAAGGGCTGTATAGGAGCCC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1242466012 Functional Loss SNV dbSNP153 33..33 33 - - - 20578 RMVar_ID_20578 Human_SNP_ID_171089981 A-to-I Human chr4 - 3506402 3506402 3506402 CGCCATTGCACTCCGGCCTGGGGACAAGAGCAAGACTTCGCCTCAAAAAAAAAAAAAAACCCAGC CGCCATTGCACTCCGGCCTGGGGACAAGAGCACGACTTCGCCTCAAAAAAAAAAAAAAACCCAGC T G LRPAP1 Ensembl:ENSG00000163956 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1191800736 Functional Loss SNV dbSNP153 33..33 33 - - - 20579 RMVar_ID_20579 Human_SNP_ID_171090224 A-to-I Human chr4 - 3507186 3507186 3507186 GTCAGGATCTTTCTCGCACAGGCTTGGAGTGCAGTGGTGCGATCATAGCTCACTGCAACCTCAAA GTCAGGATCTTTCTCGCACAGGCTTGGAGTGCGGTGGTGCGATCATAGCTCACTGCAACCTCAAA T C LRPAP1 Ensembl:ENSG00000163956 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1428600681 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15143904 20580 RMVar_ID_20580 Human_SNP_ID_171090466 A-to-I Human chr4 - 3508071 3508071 3508071 AACTCAGGAGGTGGAGGTTGCAGTGAGCTGAGATCACACCACTGCACTCCAGCCTGGGCAACAGA AACTCAGGAGGTGGAGGTTGCAGTGAGCTGAGGTCACACCACTGCACTCCAGCCTGGGCAACAGA T C LRPAP1 Ensembl:ENSG00000163956 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1007870986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_163019 20581 RMVar_ID_20581 Human_SNP_ID_171090478 A-to-I Human chr4 - 3508117 3508117 3508117 CCTGTAATCCCAGCTACTCTGGAGGCTGAGGCAGGAGAATCACTTGAACTCAGGAGGTGGAGGTT CCTGTAATCCCAGCTACTCTGGAGGCTGAGGCGGGAGAATCACTTGAACTCAGGAGGTGGAGGTT T C LRPAP1 Ensembl:ENSG00000163956 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1416395117 Functional Loss SNV dbSNP153 33..33 33 - - - 20582 RMVar_ID_20582 Human_SNP_ID_171091113 A-to-I Human chr4 - 3510321 3510321 3510321 TCGCCTCAGTCTCCTGAGTAGTAGCTGCGACCACAGGCGTGTGTCACCACACCCGGCTGATTTTA TCGCCTCAGTCTCCTGAGTAGTAGCTGCGACCCCAGGCGTGTGTCACCACACCCGGCTGATTTTA T G LRPAP1 Ensembl:ENSG00000163956 Protein coding 3'UTR GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1488565197 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15144001 Human_miRNA_ID_605184,Human_miRNA_ID_946096,Human_miRNA_ID_1054067 20583 RMVar_ID_20583 Human_SNP_ID_171092701 A-to-I Human chr4 - 3514930 3514930 3514930 AAGGGAACACTCACCTATGGAAACCTTGTTCCAGGAGGAGCTCAAGCACTTCGAAGCCAAAATCG AAGGGAACACTCACCTATGGAAACCTTGTTCCGGGAGGAGCTCAAGCACTTCGAAGCCAAAATCG T C LRPAP1 Ensembl:ENSG00000163956 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs112570687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_72867,Human_RBP_ID_163020,Human_RBP_ID_939588,Human_RBP_ID_5210006,Human_RBP_ID_9396149,Human_RBP_ID_22552745,Human_RBP_ID_22679043,Human_RBP_ID_22770382 20584 RMVar_ID_20584 Human_SNP_ID_171240930 A-to-I Human chr4 - 3943830 3943830 3943830 CCATCATGCCTGGCTAATTTTTGTATTTTTGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGC CCATCATGCCTGGCTAATTTTTGTATTTTTGTGGAGATGGGGTTTCACCATGTTGGCCAGGCTGC T C FAM86EP,AC226119.1 Ensembl:ENSG00000251669,Ensembl:ENSG00000253917 Pseudogene,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1461436773 Functional Loss SNV dbSNP153 33..33 33 - - - 20585 RMVar_ID_20585 Human_SNP_ID_171240931 A-to-I Human chr4 - 3943838 3943838 3943838 GGCACCCGCCATCATGCCTGGCTAATTTTTGTATTTTTGTAGAGATGGGGTTTCACCATGTTGGC GGCACCCGCCATCATGCCTGGCTAATTTTTGTGTTTTTGTAGAGATGGGGTTTCACCATGTTGGC T C FAM86EP,AC226119.1 Ensembl:ENSG00000251669,Ensembl:ENSG00000253917 Pseudogene,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs527984337 Functional Loss SNV dbSNP153 33..33 33 - - - 20586 RMVar_ID_20586 Human_SNP_ID_171241191 A-to-I Human chr4 - 3944477 3944477 3944477 CAAAAATTAGCCAGGCGTGGTGCTGCACGCCTATAATCCCAGCTACTCGGGATGCTGATGCAGGA CAAAAATTAGCCAGGCGTGGTGCTGCACGCCTGTAATCCCAGCTACTCGGGATGCTGATGCAGGA T C FAM86EP,AC226119.1 Ensembl:ENSG00000251669,Ensembl:ENSG00000253917 Pseudogene,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1457761473 Functional Loss SNV dbSNP153 33..33 33 - - - 20587 RMVar_ID_20587 Human_SNP_ID_171241251 A-to-I Human chr4 - 3944644 3944644 3944644 CAAAAAACTGTGATTGAAAATCATCCCGGGTCACAGTGTCTCACACCTGTAATCCCAACACTGTA CAAAAAACTGTGATTGAAAATCATCCCGGGTCCCAGTGTCTCACACCTGTAATCCCAACACTGTA T G FAM86EP,AC226119.1 Ensembl:ENSG00000251669,Ensembl:ENSG00000253917 Pseudogene,lincRNA intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs565597294 Functional Loss SNV dbSNP153 33..33 33 - - - 20588 RMVar_ID_20588 Human_SNP_ID_171241461 A-to-I Human chr4 - 3945301 3945301 3945301 TACCACACCTGGCTAATTTTTTTATTTTTTGTAGAGTCAAGGTTTTGCCATGTTGGCCAGGCTGA TACCACACCTGGCTAATTTTTTTATTTTTTGTGGAGTCAAGGTTTTGCCATGTTGGCCAGGCTGA T C FAM86EP,AC226119.1 Ensembl:ENSG00000251669,Ensembl:ENSG00000253917 Pseudogene,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1374985665 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17410099 20589 RMVar_ID_20589 Human_SNP_ID_171241475 A-to-I Human chr4 - 3945327 3945327 3945327 GAGTAGATGGGACTACAGGCAGGTGCTACCACACCTGGCTAATTTTTTTATTTTTTGTAGAGTCA GAGTAGATGGGACTACAGGCAGGTGCTACCACTCCTGGCTAATTTTTTTATTTTTTGTAGAGTCA T A FAM86EP,AC226119.1 Ensembl:ENSG00000251669,Ensembl:ENSG00000253917 Pseudogene,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1241791532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17410099 20590 RMVar_ID_20590 Human_SNP_ID_171241487 A-to-I Human chr4 - 3945345 3945345 3945345 CTCCCATCTCAGCCTCCTGAGTAGATGGGACTACAGGCAGGTGCTACCACACCTGGCTAATTTTT CTCCCATCTCAGCCTCCTGAGTAGATGGGACTTCAGGCAGGTGCTACCACACCTGGCTAATTTTT T A FAM86EP,AC226119.1 Ensembl:ENSG00000251669,Ensembl:ENSG00000253917 Pseudogene,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1224816265 Functional Loss SNV dbSNP153 33..33 33 - - - 20591 RMVar_ID_20591 Human_SNP_ID_171241656 A-to-I Human chr4 - 3945660 3945660 3945660 TGGAGGCTACAATGAGCCCTGATCTCACCACTACACTCCAGCCTGGGCAACAGAGCAAGATCCTG TGGAGGCTACAATGAGCCCTGATCTCACCACTGCACTCCAGCCTGGGCAACAGAGCAAGATCCTG T C FAM86EP,AC226119.1 Ensembl:ENSG00000251669,Ensembl:ENSG00000253917 Pseudogene,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs539194602 Functional Loss SNV dbSNP153 33..33 33 - - - 20592 RMVar_ID_20592 Human_SNP_ID_171241685 A-to-I Human chr4 - 3945743 3945743 3945743 GAAACTAGCCAGGCGTGGTTTCACACACCTGTAGTCCCAGCTACTCGGGAGGCTGAGGTGGAGGA GAAACTAGCCAGGCGTGGTTTCACACACCTGTCGTCCCAGCTACTCGGGAGGCTGAGGTGGAGGA T G FAM86EP,AC226119.1 Ensembl:ENSG00000251669,Ensembl:ENSG00000253917 Pseudogene,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1174815971 Functional Loss SNV dbSNP153 33..33 33 - - - 20593 RMVar_ID_20593 Human_SNP_ID_171241713 A-to-I Human chr4 - 3945824 3945824 3945824 AAGGCAGGAGGACTACTTGACCCCAGGTGTTCAAGACGAACCTGGGCCACATAGTGGGATCCCGT AAGGCAGGAGGACTACTTGACCCCAGGTGTTCCAGACGAACCTGGGCCACATAGTGGGATCCCGT T G FAM86EP,AC226119.1 Ensembl:ENSG00000251669,Ensembl:ENSG00000253917 Pseudogene,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1356852026 Functional Loss SNV dbSNP153 33..33 33 - - - 20594 RMVar_ID_20594 Human_SNP_ID_171351036 A-to-I Human chr4 - 4242013 4242013 4242013 CCTGTAATTCCAGCTACTTGGGAGGCTGAGGCAGGAGAATTGGTGAACCTGGGAGGCGGAGGTTG CCTGTAATTCCAGCTACTTGGGAGGCTGAGGCCGGAGAATTGGTGAACCTGGGAGGCGGAGGTTG T G TMEM128 Ensembl:ENSG00000132406 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs371745733 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_270681,RMVar_hsa_circ_224564,RMVar_hsa_circ_224563,RMVar_hsa_circ_273475 20595 RMVar_ID_20595 Human_SNP_ID_171351750 A-to-I Human chr4 - 4244355 4244355 4244355 CTCCCACCTCAGCCTCCCAAGTAGCTAGGACTATAGGCGCACACCACCATGCCTGGCTAATTTGG CTCCCACCTCAGCCTCCCAAGTAGCTAGGACTGTAGGCGCACACCACCATGCCTGGCTAATTTGG T C TMEM128 Ensembl:ENSG00000132406 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs776530408 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_270681,RMVar_hsa_circ_224564,RMVar_hsa_circ_224563,RMVar_hsa_circ_273475 20596 RMVar_ID_20596 Human_SNP_ID_171351752 A-to-I Human chr4 - 4244361 4244361 4244361 GTGATCCTCCCACCTCAGCCTCCCAAGTAGCTAGGACTATAGGCGCACACCACCATGCCTGGCTA GTGATCCTCCCACCTCAGCCTCCCAAGTAGCTGGGACTATAGGCGCACACCACCATGCCTGGCTA T C TMEM128 Ensembl:ENSG00000132406 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1028103062 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_270681,RMVar_hsa_circ_224564,RMVar_hsa_circ_224563,RMVar_hsa_circ_273475 20597 RMVar_ID_20597 Human_SNP_ID_171361911 A-to-I Human chr4 - 4279108 4279108 4279108 GTTAAGCAGGCTGGTCTCGAATTCCTGACCTCAGGTGACCTGCCTGCGTTGGCCTCCCAAAGTGC GTTAAGCAGGCTGGTCTCGAATTCCTGACCTCGGGTGACCTGCCTGCGTTGGCCTCCCAAAGTGC T C LYAR Ensembl:ENSG00000145220 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1225011980 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_224566,RMVar_hsa_circ_358433,RMVar_hsa_circ_367838,RMVar_hsa_circ_126164,RMVar_hsa_circ_224565 20598 RMVar_ID_20598 Human_SNP_ID_171361954 A-to-I Human chr4 - 4279246 4279246 4279246 CTCACTGCAACTTCTGCCTCTGGGTTCAAGCAATTCTCGTGTCTCAGCCTCCCAAGTAGCTGGGA CTCACTGCAACTTCTGCCTCTGGGTTCAAGCAGTTCTCGTGTCTCAGCCTCCCAAGTAGCTGGGA T C LYAR Ensembl:ENSG00000145220 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417981426 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_224566,RMVar_hsa_circ_358433,RMVar_hsa_circ_367838,RMVar_hsa_circ_126164,RMVar_hsa_circ_224565 20599 RMVar_ID_20599 Human_SNP_ID_171361955 A-to-I Human chr4 - 4279247 4279247 4279247 GCTCACTGCAACTTCTGCCTCTGGGTTCAAGCAATTCTCGTGTCTCAGCCTCCCAAGTAGCTGGG GCTCACTGCAACTTCTGCCTCTGGGTTCAAGCGATTCTCGTGTCTCAGCCTCCCAAGTAGCTGGG T C LYAR Ensembl:ENSG00000145220 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs551754408 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25812382 RMVar_hsa_circ_224566,RMVar_hsa_circ_358433,RMVar_hsa_circ_367838,RMVar_hsa_circ_126164,RMVar_hsa_circ_224565 20600 RMVar_ID_20600 Human_SNP_ID_171361956 A-to-I Human chr4 - 4279247 4279247 4279247 GCTCACTGCAACTTCTGCCTCTGGGTTCAAGCAATTCTCGTGTCTCAGCCTCCCAAGTAGCTGGG GCTCACTGCAACTTCTGCCTCTGGGTTCAAGCCATTCTCGTGTCTCAGCCTCCCAAGTAGCTGGG T G LYAR Ensembl:ENSG00000145220 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs551754408 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25812382 RMVar_hsa_circ_224566,RMVar_hsa_circ_358433,RMVar_hsa_circ_367838,RMVar_hsa_circ_126164,RMVar_hsa_circ_224565 20601 RMVar_ID_20601 Human_SNP_ID_171373050 A-to-I Human chr4 + 4318960 4318960 4318960 TTGCTCATGCTGCAGTGCAGTGGTGCGATCACAGCTCACTGCAGCCTCGACCTCCTGGACACAGG TTGCTCATGCTGCAGTGCAGTGGTGCGATCACGGCTCACTGCAGCCTCGACCTCCTGGACACAGG A G ZBTB49 Ensembl:ENSG00000168826 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417466410 Functional Loss SNV dbSNP153 33..33 33 - - - 20602 RMVar_ID_20602 Human_SNP_ID_171373281 A-to-I Human chr4 + 4319943 4319943 4319943 AAAATTAGCCTGGCGTGGTGTCAGGCATCTGTAATCCCAGCCACTCAGGAGGCTGAGGCAGGAGA AAAATTAGCCTGGCGTGGTGTCAGGCATCTGTTATCCCAGCCACTCAGGAGGCTGAGGCAGGAGA A T ZBTB49 Ensembl:ENSG00000168826 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1454276237 Functional Loss SNV dbSNP153 33..33 33 - - - 20603 RMVar_ID_20603 Human_SNP_ID_171409603 A-to-I Human chr4 - 4449101 4449101 4449101 TCAAGGCTGCAGTGAGCTATGATCACAACACTACACTCTAGCCTGGACAACAGAGTGAGACCTTA TCAAGGCTGCAGTGAGCTATGATCACAACACTGCACTCTAGCCTGGACAACAGAGTGAGACCTTA T C STX18 Ensembl:ENSG00000168818 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1463054701 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61144,RMVar_hsa_circ_350414,RMVar_hsa_circ_33031,RMVar_hsa_circ_335894,RMVar_hsa_circ_314569,RMVar_hsa_circ_267258 20604 RMVar_ID_20604 Human_SNP_ID_171409628 A-to-I Human chr4 - 4449229 4449229 4449229 CAACCCGGGCAATATAGTGAGATCCCATCTCTACAAAAAATTTAAAAATTAGCTGGGTGTGGTGA CAACCCGGGCAATATAGTGAGATCCCATCTCTCCAAAAAATTTAAAAATTAGCTGGGTGTGGTGA T G STX18 Ensembl:ENSG00000168818 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1376870368 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61144,RMVar_hsa_circ_350414,RMVar_hsa_circ_33031,RMVar_hsa_circ_335894,RMVar_hsa_circ_314569,RMVar_hsa_circ_267258 20605 RMVar_ID_20605 Human_SNP_ID_171430331 A-to-I Human chr4 - 4530743 4530743 4530743 AAATTAGCCTGCCGCTTTGGCACACACCTGTAATCTCAGCTACCCGGGAGGCTGAGGTGGGAGGA AAATTAGCCTGCCGCTTTGGCACACACCTGTAGTCTCAGCTACCCGGGAGGCTGAGGTGGGAGGA T C STX18 Ensembl:ENSG00000168818 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1401163940 Functional Loss SNV dbSNP153 33..33 33 - - - 20606 RMVar_ID_20606 Human_SNP_ID_171434440 A-to-I Human chr4 + 4546526 4546526 4546526 GCAATTCTCCTTCTTCAGCCTCCCAAGTAGCTAGGATTACAGACGTCCTCCACCATGCCCAGCTA GCAATTCTCCTTCTTCAGCCTCCCAAGTAGCTGGGATTACAGACGTCCTCCACCATGCCCAGCTA A G STX18-AS1 Ensembl:ENSG00000247708 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559004081 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_224578,RMVar_hsa_circ_224577,RMVar_hsa_circ_120232,RMVar_hsa_circ_85114 20607 RMVar_ID_20607 Human_SNP_ID_171435977 A-to-I Human chr4 + 4552212 4552212 4552212 AGGGGCCAGGGACAGAATGATGTGGTTTGGCTATGTCCCCATTCAAATCTCAACTTGTATCTCCC AGGGGCCAGGGACAGAATGATGTGGTTTGGCTGTGTCCCCATTCAAATCTCAACTTGTATCTCCC A G STX18-AS1 Ensembl:ENSG00000247708 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs763306503 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_224578,RMVar_hsa_circ_224577,RMVar_hsa_circ_120232,RMVar_hsa_circ_85114 20608 RMVar_ID_20608 Human_SNP_ID_171471839 A-to-I Human chr4 + 4692909 4692909 4692909 TCCCAGCTACTCGAGAGGCTGAGAAGCATGAGAATCAATTGAATCCAGGAGGTGGAGGTTGCAGT TCCCAGCTACTCGAGAGGCTGAGAAGCATGAGCATCAATTGAATCCAGGAGGTGGAGGTTGCAGT A C STX18-AS1 Ensembl:ENSG00000247708 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041924524 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_307790,RMVar_hsa_circ_77701,RMVar_hsa_circ_224584,RMVar_hsa_circ_224586 20609 RMVar_ID_20609 Human_SNP_ID_171474366 A-to-I Human chr4 + 4701361 4701361 4701361 GCTCAAATGCTGGAGTGCAGTGGCATGATCTCAGCTCACTGCAAGCTCTGCCTCCCAGGTTCACA GCTCAAATGCTGGAGTGCAGTGGCATGATCTCGGCTCACTGCAAGCTCTGCCTCCCAGGTTCACA A G STX18-AS1 Ensembl:ENSG00000247708 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1376283103 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_307790,RMVar_hsa_circ_77701,RMVar_hsa_circ_224584,RMVar_hsa_circ_224586 20610 RMVar_ID_20610 Human_SNP_ID_171987878 A-to-I Human chr4 - 6462996 6462996 6462996 AGGGAGTGCACCTTCCCCCCTCCCTCTGTCCCAGAGAAGGGAGAGATGCCGCTCCCTGGAGCCCC AGGGAGTGCACCTTCCCCCCTCCCTCTGTCCCGGAGAAGGGAGAGATGCCGCTCCCTGGAGCCCC T C PPP2R2C Ensembl:ENSG00000074211 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1560566591 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_276581 20611 RMVar_ID_20611 Human_SNP_ID_172032126 A-to-I Human chr4 + 6623044 6623044 6623044 GCAGGAGCCCTTTAGAGCATGTGGGCTGCATGAGGCTTGGTTTCTGTGTCAAGAAGACTATGGAG GCAGGAGCCCTTTAGAGCATGTGGGCTGCATGGGGCTTGGTTTCTGTGTCAAGAAGACTATGGAG A G MAN2B2 Ensembl:ENSG00000013288 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs4435813 Functional Loss SNV dbSNP153 33..33 33 - - - 20612 RMVar_ID_20612 Human_SNP_ID_172032127 A-to-I Human chr4 + 6623044 6623044 6623044 GCAGGAGCCCTTTAGAGCATGTGGGCTGCATGAGGCTTGGTTTCTGTGTCAAGAAGACTATGGAG GCAGGAGCCCTTTAGAGCATGTGGGCTGCATGTGGCTTGGTTTCTGTGTCAAGAAGACTATGGAG A T MAN2B2 Ensembl:ENSG00000013288 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs4435813 Functional Loss SNV dbSNP153 33..33 33 - - - 20613 RMVar_ID_20613 Human_SNP_ID_172054887 A-to-I Human chr4 - 6696890 6696886 6696891 TTTATCCACGGCATCCTTGTCTTTTCCACTCTAGAGGAGAGAGAGGCTCAAGGTCAGCAGTGAGG TTTATCCACGGCATCCTTGTCTTTTCCACTC_____GAGAGAGAGGCTCAAGGTCAGCAGTGAGG CCTCTA C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1227641453 Functional Loss DEL dbSNP153 32..36 33 - - - 20614 RMVar_ID_20614 Human_SNP_ID_172054889 A-to-I Human chr4 - 6696890 6696890 6696890 TTTATCCACGGCATCCTTGTCTTTTCCACTCTAGAGGAGAGAGAGGCTCAAGGTCAGCAGTGAGG TTTATCCACGGCATCCTTGTCTTTTCCACTCTGGAGGAGAGAGAGGCTCAAGGTCAGCAGTGAGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs746368083 Functional Loss SNV dbSNP153 33..33 33 - - - 20615 RMVar_ID_20615 Human_SNP_ID_172082824 A-to-I Human chr4 + 6787060 6787060 6787060 AAAATTATCCGGGCATGGTGGAGCACGCCTATAGTCCCAGCTACTTGGGAGGCTGAGGCAGTAGA AAAATTATCCGGGCATGGTGGAGCACGCCTATCGTCCCAGCTACTTGGGAGGCTGAGGCAGTAGA A C KIAA0232 Ensembl:ENSG00000170871 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs867105962 Functional Loss SNV dbSNP153 33..33 33 - - - 20616 RMVar_ID_20616 Human_SNP_ID_172083502 A-to-I Human chr4 + 6789403 6789403 6789403 TCAAGTGATTCTCCTGCCTCAGACTCCCCAGTAGCTGGGATTACAGGTGCGTGCCACCATGCCCG TCAAGTGATTCTCCTGCCTCAGACTCCCCAGTCGCTGGGATTACAGGTGCGTGCCACCATGCCCG A C KIAA0232 Ensembl:ENSG00000170871 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1048086479 Functional Loss SNV dbSNP153 33..33 33 - - - 20617 RMVar_ID_20617 Human_SNP_ID_172086790 A-to-I Human chr4 + 6800566 6800566 6800566 AGCTGGGTGTGGTGGTATGCACCTGTAATCCCAGCTACGCAGGAGGCTGATGCAGGAGAATCACT AGCTGGGTGTGGTGGTATGCACCTGTAATCCCGGCTACGCAGGAGGCTGATGCAGGAGAATCACT A G KIAA0232 Ensembl:ENSG00000170871 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1179631322 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_163262 20618 RMVar_ID_20618 Human_SNP_ID_172088666 A-to-I Human chr4 + 6807168 6807168 6807168 GTGTTGTTCCTGCCTCAGCTTCTCCAATAGCTAGGATTATAGGCACACACCATGGCATCCAGCTT GTGTTGTTCCTGCCTCAGCTTCTCCAATAGCTGGGATTATAGGCACACACCATGGCATCCAGCTT A G KIAA0232 Ensembl:ENSG00000170871 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs939859356 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75788,RMVar_hsa_circ_334365,RMVar_hsa_circ_306519,RMVar_hsa_circ_224689 20619 RMVar_ID_20619 Human_SNP_ID_172128045 A-to-I Human chr4 + 6945584 6945584 6945584 CAGCCTGACCAACATGGAGAAACCCCGTCTCTACTAAAAATGCAAAATTAGCCGAGCGTGGTGGC CAGCCTGACCAACATGGAGAAACCCCGTCTCTGCTAAAAATGCAAAATTAGCCGAGCGTGGTGGC A G TBC1D14 Ensembl:ENSG00000132405 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs575496994 Functional Loss SNV dbSNP153 33..33 33 - - - 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 20620 RMVar_ID_20620 Human_SNP_ID_172128046 A-to-I Human chr4 + 6945587 6945587 6945587 CCTGACCAACATGGAGAAACCCCGTCTCTACTAAAAATGCAAAATTAGCCGAGCGTGGTGGCAAC CCTGACCAACATGGAGAAACCCCGTCTCTACTGAAAATGCAAAATTAGCCGAGCGTGGTGGCAAC A G TBC1D14 Ensembl:ENSG00000132405 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1041453554 Functional Loss SNV dbSNP153 33..33 33 - - - 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 20621 RMVar_ID_20621 Human_SNP_ID_172147211 A-to-I Human chr4 + 7011683 7011683 7011683 GGTTCAAGCAATTATCGTGTCTCAGCCTCCCTAGTAGCTGGGATTACAGGTGTCTGCCACCATGC GGTTCAAGCAATTATCGTGTCTCAGCCTCCCTGGTAGCTGGGATTACAGGTGTCTGCCACCATGC A G TBC1D14 Ensembl:ENSG00000132405 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1444788961 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54238,RMVar_hsa_circ_301538,RMVar_hsa_circ_354634,RMVar_hsa_circ_224701,RMVar_hsa_circ_286641,RMVar_hsa_circ_10947,RMVar_hsa_circ_224711,RMVar_hsa_circ_332784,RMVar_hsa_circ_224721,RMVar_hsa_circ_285881,RMVar_hsa_circ_12173,RMVar_hsa_circ_289958,RMVar_hsa_circ_337492,RMVar_hsa_circ_224730,RMVar_hsa_circ_224723,RMVar_hsa_circ_224724,RMVar_hsa_circ_282236,RMVar_hsa_circ_284187,RMVar_hsa_circ_224729,RMVar_hsa_circ_361920,RMVar_hsa_circ_324617 20622 RMVar_ID_20622 Human_SNP_ID_172152824 A-to-I Human chr4 + 7029678 7029678 7029678 GAAACCCTGTCTGTACTAAAAATACAAAAATTAGCCAGGCGTGGTGGCACACCTCTGTATTCCCA GAAACCCTGTCTGTACTAAAAATACAAAAATTCGCCAGGCGTGGTGGCACACCTCTGTATTCCCA A C TBC1D14 Ensembl:ENSG00000132405 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs568952424 Functional Loss SNV dbSNP153 33..33 33 - - - 20623 RMVar_ID_20623 Human_SNP_ID_172152835 A-to-I Human chr4 + 7029714 7029714 7029714 AGGCGTGGTGGCACACCTCTGTATTCCCAGCTACTCAGGAGGCTGAGGCAGAAGAATCTCTTGAA AGGCGTGGTGGCACACCTCTGTATTCCCAGCTGCTCAGGAGGCTGAGGCAGAAGAATCTCTTGAA A G TBC1D14 Ensembl:ENSG00000132405 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs965789158 Functional Loss SNV dbSNP153 33..33 33 - - - 20624 RMVar_ID_20624 Human_SNP_ID_172152853 A-to-I Human chr4 + 7029764 7029764 7029764 GAAGAATCTCTTGAACCCGGGGGTCAGAGATTACAGTGAGCCGAGATGGCGCCACTCCACTCCAG GAAGAATCTCTTGAACCCGGGGGTCAGAGATTCCAGTGAGCCGAGATGGCGCCACTCCACTCCAG A C TBC1D14 Ensembl:ENSG00000132405 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs923957564 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_213728 20625 RMVar_ID_20625 Human_SNP_ID_172152855 A-to-I Human chr4 + 7029766 7029766 7029766 AGAATCTCTTGAACCCGGGGGTCAGAGATTACAGTGAGCCGAGATGGCGCCACTCCACTCCAGCC AGAATCTCTTGAACCCGGGGGTCAGAGATTACGGTGAGCCGAGATGGCGCCACTCCACTCCAGCC A G TBC1D14 Ensembl:ENSG00000132405 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1217343037 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_213728 20626 RMVar_ID_20626 Human_SNP_ID_172163664 A-to-I Human chr4 - 7064687 7064687 7064687 CAAGACTAGCCTGGCCAACATAGTGAAACCCCATCGCTACTAAAAATACAAAAATTAGCCGGGTG CAAGACTAGCCTGGCCAACATAGTGAAACCCCGTCGCTACTAAAAATACAAAAATTAGCCGGGTG T C GRPEL1 Ensembl:ENSG00000109519 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs898019264 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93254,RMVar_hsa_circ_224734 20627 RMVar_ID_20627 Human_SNP_ID_172164030 A-to-I Human chr4 - 7065982 7065982 7065982 GAGCGTGTTGGTGGACGCCTATAGTCCCAGCTACTCGGCAGGCTGAGGCAGGAGAATGGCGTGAA GAGCGTGTTGGTGGACGCCTATAGTCCCAGCTCCTCGGCAGGCTGAGGCAGGAGAATGGCGTGAA T G GRPEL1 Ensembl:ENSG00000109519 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs572664419 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93254,RMVar_hsa_circ_224734 20628 RMVar_ID_20628 Human_SNP_ID_172164034 A-to-I Human chr4 - 7065994 7065994 7065994 AAAAAATTAGCCGAGCGTGTTGGTGGACGCCTATAGTCCCAGCTACTCGGCAGGCTGAGGCAGGA AAAAAATTAGCCGAGCGTGTTGGTGGACGCCTGTAGTCCCAGCTACTCGGCAGGCTGAGGCAGGA T C GRPEL1 Ensembl:ENSG00000109519 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1436533763 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93254,RMVar_hsa_circ_224734 20629 RMVar_ID_20629 Human_SNP_ID_172322150 A-to-I Human chr4 + 7582601 7582600 7582601 TTTCATATGTAGCAGAGCAGCTCCCTCGCTGCAATCTATTGAAAGTCAGCCCTCGACACAAGGGT TTTCATATGTAGCAGAGCAGCTCCCTCGCTGC_ATCTATTGAAAGTCAGCCCTCGACACAAGGGT CA C SORCS2 Ensembl:ENSG00000184985 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1553887948 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_72998,Human_RBP_ID_163499,Human_RBP_ID_270578,Human_RBP_ID_1107774,Human_RBP_ID_1139756,Human_RBP_ID_1209239,Human_RBP_ID_1317646,Human_RBP_ID_1641952,Human_RBP_ID_1980871,Human_RBP_ID_2871024,Human_RBP_ID_5276251,Human_RBP_ID_5301010,Human_RBP_ID_8265856,Human_RBP_ID_8594534,Human_RBP_ID_9162754,Human_RBP_ID_9341463,Human_RBP_ID_10154701,Human_RBP_ID_15198215,Human_RBP_ID_17671523,Human_RBP_ID_17706129,Human_RBP_ID_18029250,Human_RBP_ID_18471849,Human_RBP_ID_18517760,Human_RBP_ID_18537630,Human_RBP_ID_18828376,Human_RBP_ID_19123360,Human_RBP_ID_20977573,Human_RBP_ID_21898974,Human_RBP_ID_22293072,Human_RBP_ID_22401948,Human_RBP_ID_22458135,Human_RBP_ID_22826764,Human_RBP_ID_23033531,Human_RBP_ID_23191233,Human_RBP_ID_23313633,Human_RBP_ID_24063923,Human_RBP_ID_24430367,Human_RBP_ID_24547763,Human_RBP_ID_25820366,Human_RBP_ID_26516714,Human_RBP_ID_26694913,Human_RBP_ID_27070011,Human_RBP_ID_27160171,Human_RBP_ID_27328495 20630 RMVar_ID_20630 Human_SNP_ID_172322152 A-to-I Human chr4 + 7582601 7582601 7582601 TTTCATATGTAGCAGAGCAGCTCCCTCGCTGCAATCTATTGAAAGTCAGCCCTCGACACAAGGGT TTTCATATGTAGCAGAGCAGCTCCCTCGCTGCGATCTATTGAAAGTCAGCCCTCGACACAAGGGT A G SORCS2 Ensembl:ENSG00000184985 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs75476276 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_72998,Human_RBP_ID_163499,Human_RBP_ID_270578,Human_RBP_ID_1107774,Human_RBP_ID_1139756,Human_RBP_ID_1209239,Human_RBP_ID_1317646,Human_RBP_ID_1641952,Human_RBP_ID_1980871,Human_RBP_ID_2871024,Human_RBP_ID_5276251,Human_RBP_ID_5301010,Human_RBP_ID_8265856,Human_RBP_ID_8594534,Human_RBP_ID_9162754,Human_RBP_ID_9341463,Human_RBP_ID_10154701,Human_RBP_ID_15198215,Human_RBP_ID_17671523,Human_RBP_ID_17706129,Human_RBP_ID_18029250,Human_RBP_ID_18471849,Human_RBP_ID_18517760,Human_RBP_ID_18537630,Human_RBP_ID_18828376,Human_RBP_ID_19123360,Human_RBP_ID_20977573,Human_RBP_ID_21898974,Human_RBP_ID_22293072,Human_RBP_ID_22401948,Human_RBP_ID_22458135,Human_RBP_ID_22826764,Human_RBP_ID_23033531,Human_RBP_ID_23191233,Human_RBP_ID_23313633,Human_RBP_ID_24063923,Human_RBP_ID_24430367,Human_RBP_ID_24547763,Human_RBP_ID_25820366,Human_RBP_ID_26516714,Human_RBP_ID_26694913,Human_RBP_ID_27070011,Human_RBP_ID_27160171,Human_RBP_ID_27328495 20631 RMVar_ID_20631 Human_SNP_ID_172418596 A-to-I Human chr4 - 7872993 7872993 7872993 CGCCTGCCTGGGTCTCCCAAAGTGCTGGGATTACAGACGTGAGCCACCGCGCCCAGCCCAAGTAG CGCCTGCCTGGGTCTCCCAAAGTGCTGGGATTGCAGACGTGAGCCACCGCGCCCAGCCCAAGTAG T C AFAP1 Ensembl:ENSG00000196526 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1490557930 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_224775 20632 RMVar_ID_20632 Human_SNP_ID_172449043 A-to-I Human chr4 - 7973548 7973548 7973548 AGGGCCTATCCTGTCCTCACCTTTCCCGGCTCAGGTCCAGACACCTCAGCTTTCTTTTTTTTCTC AGGGCCTATCCTGTCCTCACCTTTCCCGGCTCCGGTCCAGACACCTCAGCTTTCTTTTTTTTCTC T G ABLIM2 Ensembl:ENSG00000163995 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs747516625 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_224778 20633 RMVar_ID_20633 Human_SNP_ID_172518640 A-to-I Human chr4 + 8203606 8203606 8203606 GTCTAACGCAGGCCCAGCTTGCCCTGTTTGGTAAAAAACTGAGGTGGGGAAGAAATAAGCCCAGC GTCTAACGCAGGCCCAGCTTGCCCTGTTTGGTTAAAAACTGAGGTGGGGAAGAAATAAGCCCAGC A T SH3TC1 Ensembl:ENSG00000125089 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417128908 Functional Loss SNV dbSNP153 33..33 33 - - - 20634 RMVar_ID_20634 Human_SNP_ID_172595517 A-to-I Human chr4 + 8454609 8454609 8454609 GCACCTGGTGCGCTGGACACATCAGGATGGGTATGAGTTGCTGGCAGGAAGCTCTTCTCTTGCCC GCACCTGGTGCGCTGGACACATCAGGATGGGTGTGAGTTGCTGGCAGGAAGCTCTTCTCTTGCCC A G TRMT44 Ensembl:ENSG00000155275 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1024631395 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_52245,RMVar_hsa_circ_7235,RMVar_hsa_circ_64709,RMVar_hsa_circ_293683,RMVar_hsa_circ_224801 20635 RMVar_ID_20635 Human_SNP_ID_172596545 A-to-I Human chr4 + 8458532 8458532 8458532 GTCGCCCAGGCTGGAGTGCAGTGGTGTGATCTAGGTTCACTGCAACCTCTGCCTTCCAGGTTCAA GTCGCCCAGGCTGGAGTGCAGTGGTGTGATCTGGGTTCACTGCAACCTCTGCCTTCCAGGTTCAA A G TRMT44 Ensembl:ENSG00000155275 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs566696880 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7235,RMVar_hsa_circ_64709 20636 RMVar_ID_20636 Human_SNP_ID_174100555 A-to-I Human chr4 - 13337005 13337005 13337005 TCTTTAAGGTGGAGGATCACTTTGGTACCCCTACCAATAGGCTCACCATGGTCAGCACACACAGT TCTTTAAGGTGGAGGATCACTTTGGTACCCCTGCCAATAGGCTCACCATGGTCAGCACACACAGT T C lnc-RAB28-5 RNACentral:URS00008B7EF7 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs763688073 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97367,RMVar_hsa_circ_224858,RMVar_hsa_circ_224859,RMVar_hsa_circ_224860 20637 RMVar_ID_20637 Human_SNP_ID_174100762 A-to-I Human chr4 - 13337912 13337912 13337912 TCTCACCAGTGATGTAATAGATGGACTTCTGTATCTCCTTCATGCGAGAAACATACTCTAACAAA TCTCACCAGTGATGTAATAGATGGACTTCTGTGTCTCCTTCATGCGAGAAACATACTCTAACAAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1391425482 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97367,RMVar_hsa_circ_224858,RMVar_hsa_circ_224859,RMVar_hsa_circ_224860 20638 RMVar_ID_20638 Human_SNP_ID_174181510 A-to-I Human chr4 + 13647813 13647813 13647813 GTTCAATTAAATGTAGCCTCATCTTAATCAATAATATCAATGAAATCACATATCTGATGTGATGG GTTCAATTAAATGTAGCCTCATCTTAATCAATGATATCAATGAAATCACATATCTGATGTGATGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1390367237 Functional Loss SNV dbSNP153 33..33 33 - - - 20639 RMVar_ID_20639 Human_SNP_ID_31808869 A-to-I Human chr1 - 143540743 143540743 143540743 ATCATCATCGAATGGAATCAAATGGAATCATCAAATGGACTGGAATGGAATCATTGAATGGACTC ATCATCATCGAATGGAATCAAATGGAATCATCTAATGGACTGGAATGGAATCATTGAATGGACTC T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs61786640 Functional Loss SNV dbSNP153 33..33 33 - - - 20640 RMVar_ID_20640 Human_SNP_ID_31808870 A-to-I Human chr1 - 143540743 143540743 143540743 ATCATCATCGAATGGAATCAAATGGAATCATCAAATGGACTGGAATGGAATCATTGAATGGACTC ATCATCATCGAATGGAATCAAATGGAATCATCGAATGGACTGGAATGGAATCATTGAATGGACTC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs61786640 Functional Loss SNV dbSNP153 33..33 33 - - - 20641 RMVar_ID_20641 Human_SNP_ID_31808871 A-to-I Human chr1 - 143540743 143540743 143540743 ATCATCATCGAATGGAATCAAATGGAATCATCAAATGGACTGGAATGGAATCATTGAATGGACTC ATCATCATCGAATGGAATCAAATGGAATCATCCAATGGACTGGAATGGAATCATTGAATGGACTC T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs61786640 Functional Loss SNV dbSNP153 33..33 33 - - - 20642 RMVar_ID_20642 Human_SNP_ID_31808885 A-to-I Human chr1 - 143540755 143540755 143540755 GAATGAAATGGAATCATCATCGAATGGAATCAAATGGAATCATCAAATGGACTGGAATGGAATCA GAATGAAATGGAATCATCATCGAATGGAATCAGATGGAATCATCAAATGGACTGGAATGGAATCA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs78106680 Functional Loss SNV dbSNP153 33..33 33 - - - 20643 RMVar_ID_20643 Human_SNP_ID_31830113 A-to-I Human chr1 - 143594397 143594397 143594397 TGCATAATGTAGAGCACTGAGCAGGACAGCTGACCTGTCTCCTTCACACAGTCCATGTCACCACG TGCATAATGTAGAGCACTGAGCAGGACAGCTGGCCTGTCTCCTTCACACAGTCCATGTCACCACG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1181863368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23303842 20644 RMVar_ID_20644 Human_SNP_ID_31881983 A-to-I Human chr1 - 143729373 143729373 143729373 TTTTTTGTAGTTTAAAGAATAGTCTACACAGCAAGGGTTACTTGTTTTTTTTACTGGCTTGTGTT TTTTTTGTAGTTTAAAGAATAGTCTACACAGCGAGGGTTACTTGTTTTTTTTACTGGCTTGTGTT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs112716611 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5684967,Human_RBP_ID_18216363,Human_RBP_ID_23121326 20645 RMVar_ID_20645 Human_SNP_ID_31881984 A-to-I Human chr1 - 143729373 143729373 143729373 TTTTTTGTAGTTTAAAGAATAGTCTACACAGCAAGGGTTACTTGTTTTTTTTACTGGCTTGTGTT TTTTTTGTAGTTTAAAGAATAGTCTACACAGCCAGGGTTACTTGTTTTTTTTACTGGCTTGTGTT T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs112716611 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5684967,Human_RBP_ID_18216363,Human_RBP_ID_23121326 20646 RMVar_ID_20646 Human_SNP_ID_31881987 A-to-I Human chr1 - 143729376 143729376 143729376 TGATTTTTTGTAGTTTAAAGAATAGTCTACACAGCAAGGGTTACTTGTTTTTTTTACTGGCTTGT TGATTTTTTGTAGTTTAAAGAATAGTCTACACGGCAAGGGTTACTTGTTTTTTTTACTGGCTTGT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs111728776 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5684967,Human_RBP_ID_23121326 20647 RMVar_ID_20647 Human_SNP_ID_31881993 A-to-I Human chr1 - 143729380 143729380 143729380 CCCCTGATTTTTTGTAGTTTAAAGAATAGTCTACACAGCAAGGGTTACTTGTTTTTTTTACTGGC CCCCTGATTTTTTGTAGTTTAAAGAATAGTCTGCACAGCAAGGGTTACTTGTTTTTTTTACTGGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs112016635 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5684967 20648 RMVar_ID_20648 Human_SNP_ID_31881994 A-to-I Human chr1 - 143729380 143729380 143729380 CCCCTGATTTTTTGTAGTTTAAAGAATAGTCTACACAGCAAGGGTTACTTGTTTTTTTTACTGGC CCCCTGATTTTTTGTAGTTTAAAGAATAGTCTCCACAGCAAGGGTTACTTGTTTTTTTTACTGGC T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs112016635 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5684967 20649 RMVar_ID_20649 Human_SNP_ID_32273558 A-to-I Human chr1 - 145691748 145691748 145691748 TGGAGTGCAGTGGTGCGATCTCGGCTCACAGCAACCTCTCTGCCTCCAGGTTCAAGCCATCCTCC TGGAGTGCAGTGGTGCGATCTCGGCTCACAGCGACCTCTCTGCCTCCAGGTTCAAGCCATCCTCC T C PDZK1 Ensembl:ENSG00000174827 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202442320 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_118317 20650 RMVar_ID_20650 Human_SNP_ID_32282196 A-to-I Human chr1 - 145730233 145730233 145730233 TCACTGCACCTTTGAACTCCTGGGCTCAAGCAATCCTCCTGCTTCCGCCTTCCGAATAGCTAACA TCACTGCACCTTTGAACTCCTGGGCTCAAGCATTCCTCCTGCTTCCGCCTTCCGAATAGCTAACA T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs868994802 Functional Loss SNV dbSNP153 33..33 33 - - - 20651 RMVar_ID_20651 Human_SNP_ID_32282197 A-to-I Human chr1 - 145730233 145730233 145730233 TCACTGCACCTTTGAACTCCTGGGCTCAAGCAATCCTCCTGCTTCCGCCTTCCGAATAGCTAACA TCACTGCACCTTTGAACTCCTGGGCTCAAGCAGTCCTCCTGCTTCCGCCTTCCGAATAGCTAACA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs868994802 Functional Loss SNV dbSNP153 33..33 33 - - - 20652 RMVar_ID_20652 Human_SNP_ID_32282947 A-to-I Human chr1 - 145733300 145733296 145733300 ACCCCGTCTCAACTAAAAATACAAAAAAAATTAGTTGGATGGGTGGTGGCGTGTGCCTGTAGTCC ACCCCGTCTCAACTAAAAATACAAAAAAAATT____GGATGGGTGGTGGCGTGTGCCTGTAGTCC CAACT C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs782813962 Functional Loss DEL dbSNP153 33..36 33 - - - 20653 RMVar_ID_20653 Human_SNP_ID_32285837 A-to-I Human chr1 - 145745275 145745275 145745275 TGCCTGGGTAATTTTTGTATTTTTGTAGAGATAGGGTTTTGCCGTGTTGCCCAGGCTGGTCTCAA TGCCTGGGTAATTTTTGTATTTTTGTAGAGATTGGGTTTTGCCGTGTTGCCCAGGCTGGTCTCAA T A RNF115 Ensembl:ENSG00000265491 Protein coding 3'UTR GSE38233;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,32596459 RNA-Seq:(High) rs1052618395 Functional Loss SNV dbSNP153 33..33 33 - - - 20654 RMVar_ID_20654 Human_SNP_ID_32285858 A-to-I Human chr1 - 145745370 145745370 145745370 ACGATCTCAGCTCACCACAGCCTCGACCTCCCAGGCTCAAGTGATCCTCCCACCTCAGCCTACCA ACGATCTCAGCTCACCACAGCCTCGACCTCCCGGGCTCAAGTGATCCTCCCACCTCAGCCTACCA T C RNF115 Ensembl:ENSG00000265491 Protein coding 3'UTR GSE38233;GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;ASD brains,temporal_cortex;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,30559470,31158229 RNA-Seq:(High) rs1378794966 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10560630,Human_RBP_ID_18550332 20655 RMVar_ID_20655 Human_SNP_ID_32285865 A-to-I Human chr1 - 145745394 145745394 145745394 TCGCCTAGGCTGGAGTGCAGTGGCACGATCTCAGCTCACCACAGCCTCGACCTCCCAGGCTCAAG TCGCCTAGGCTGGAGTGCAGTGGCACGATCTCGGCTCACCACAGCCTCGACCTCCCAGGCTCAAG T C RNF115 Ensembl:ENSG00000265491 Protein coding 3'UTR GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459,32596459 RNA-Seq:(High) rs1256698349 Functional Loss SNV dbSNP153 33..33 33 - - - 20656 RMVar_ID_20656 Human_SNP_ID_32285916 A-to-I Human chr1 - 145745550 145745550 145745550 ATGAGGCTGAGGTGGGAGAATCGCTTGAACCCAGGAGGTGGAGGTTGCGGTGAGCCGGATCATAC ATGAGGCTGAGGTGGGAGAATCGCTTGAACCCGGGAGGTGGAGGTTGCGGTGAGCCGGATCATAC T C RNF115 Ensembl:ENSG00000265491 Protein coding 3'UTR GSE38233;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29796672,31158229,32596459 RNA-Seq:(High) rs1389781711 Functional Loss SNV dbSNP153 33..33 33 - - - 20657 RMVar_ID_20657 Human_SNP_ID_32285924 A-to-I Human chr1 - 145745595 145745595 145745595 AAATTAGCTGGGCGTGGTGGTGCATGCCTGTAATCCCAGCTACTCATGAGGCTGAGGTGGGAGAA AAATTAGCTGGGCGTGGTGGTGCATGCCTGTAGTCCCAGCTACTCATGAGGCTGAGGTGGGAGAA T C RNF115 Ensembl:ENSG00000265491 Protein coding 3'UTR GSE38233;GSE99789 cultured B-cells;esophageal squamous carcinoma cells,EC109 - 24183664,29796672 RNA-Seq:(High) rs1236369537 Functional Loss SNV dbSNP153 33..33 33 - - - 20658 RMVar_ID_20658 Human_SNP_ID_32285937 A-to-I Human chr1 - 145745633 145745633 145745633 GGCCAACAAGGTAAAACCTTGTCTCTACTAAAAATATAAAATTAGCTGGGCGTGGTGGTGCATGC GGCCAACAAGGTAAAACCTTGTCTCTACTAAACATATAAAATTAGCTGGGCGTGGTGGTGCATGC T G RNF115 Ensembl:ENSG00000265491 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1330121153 Functional Loss SNV dbSNP153 33..33 33 - - - 20659 RMVar_ID_20659 Human_SNP_ID_32285939 A-to-I Human chr1 - 145745657 145745657 145745657 AGGTCAAGAGATCAAGACCAGCCTGGCCAACAAGGTAAAACCTTGTCTCTACTAAAAATATAAAA AGGTCAAGAGATCAAGACCAGCCTGGCCAACATGGTAAAACCTTGTCTCTACTAAAAATATAAAA T A RNF115 Ensembl:ENSG00000265491 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1553711622 Functional Loss SNV dbSNP153 33..33 33 - - - 20660 RMVar_ID_20660 Human_SNP_ID_32286063 A-to-I Human chr1 - 145746164 145746164 145746164 TGAAGTGCAGTGGCACGATCTTGGCTCATTGCAAACTCTGCCTCCTGAGTTCAAGCGATTCTCCT TGAAGTGCAGTGGCACGATCTTGGCTCATTGCGAACTCTGCCTCCTGAGTTCAAGCGATTCTCCT T C RNF115 Ensembl:ENSG00000265491 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1553711717 Functional Loss SNV dbSNP153 33..33 33 - - - 20661 RMVar_ID_20661 Human_SNP_ID_32294115 A-to-I Human chr1 - 145775458 145775458 145775458 CTAGGAGATTGAGGCTGCAGTGAACCATGATCACGGCGTTGCACTCCAGCCTGAGCGACCGAGTT CTAGGAGATTGAGGCTGCAGTGAACCATGATCGCGGCGTTGCACTCCAGCCTGAGCGACCGAGTT T C RNF115 Ensembl:ENSG00000265491 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1389550596 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5683721,Human_RBP_ID_10560304,Human_RBP_ID_17557300,Human_RBP_ID_24582031 RMVar_hsa_circ_331188,RMVar_hsa_circ_291164,RMVar_hsa_circ_329956,RMVar_hsa_circ_271035,RMVar_hsa_circ_315226,RMVar_hsa_circ_296392,RMVar_hsa_circ_340224 20662 RMVar_ID_20662 Human_SNP_ID_32294127 A-to-I Human chr1 - 145775524 145775524 145775524 GAGTGTGATGGTACATCCCTGTAGTCCTAGCTACTTGGGAGATTGAGGTGGGAGGATCACTTGAG GAGTGTGATGGTACATCCCTGTAGTCCTAGCTGCTTGGGAGATTGAGGTGGGAGGATCACTTGAG T C RNF115 Ensembl:ENSG00000265491 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs587628290 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10560303,Human_RBP_ID_17557300 RMVar_hsa_circ_331188,RMVar_hsa_circ_291164,RMVar_hsa_circ_329956,RMVar_hsa_circ_271035,RMVar_hsa_circ_315226,RMVar_hsa_circ_296392,RMVar_hsa_circ_340224 20663 RMVar_ID_20663 Human_SNP_ID_32294432 A-to-I Human chr1 - 145776678 145776678 145776678 GCATGCTCCACCACGCCCAGCTAACTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGCTAG GCATGCTCCACCACGCCCAGCTAACTTTTTGTGTTTTTAGTAGAGACGGGGTTTCACCATGCTAG T C RNF115 Ensembl:ENSG00000265491 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1553716625 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10560279 RMVar_hsa_circ_331188,RMVar_hsa_circ_291164,RMVar_hsa_circ_329956,RMVar_hsa_circ_271035,RMVar_hsa_circ_315226,RMVar_hsa_circ_296392,RMVar_hsa_circ_340224 20664 RMVar_ID_20664 Human_SNP_ID_32295948 A-to-I Human chr1 - 145783100 145783100 145783100 GCAACACTTTGGGAGGCCGAGGTGAGCAGATCACCTGAGGTCTGGAGTTCGAGACCAGCCTAGCC GCAACACTTTGGGAGGCCGAGGTGAGCAGATCGCCTGAGGTCTGGAGTTCGAGACCAGCCTAGCC T C RNF115 Ensembl:ENSG00000265491 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1553717684 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_331188,RMVar_hsa_circ_291164,RMVar_hsa_circ_329956,RMVar_hsa_circ_271035,RMVar_hsa_circ_315226,RMVar_hsa_circ_296392,RMVar_hsa_circ_340224 20665 RMVar_ID_20665 Human_SNP_ID_32298874 A-to-I Human chr1 - 145794017 145794017 145794017 CATCGTGGCGAAACACCGTCTCTACTAGAAATACAAAAATTAGCCGGGTGTGGTGGCACATGCCT CATCGTGGCGAAACACCGTCTCTACTAGAAATGCAAAAATTAGCCGGGTGTGGTGGCACATGCCT T C RNF115 Ensembl:ENSG00000265491 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs782299358 Functional Loss SNV dbSNP153 33..33 33 - - - 20666 RMVar_ID_20666 Human_SNP_ID_32298877 A-to-I Human chr1 - 145794023 145794023 145794023 CCTGGCCATCGTGGCGAAACACCGTCTCTACTAGAAATACAAAAATTAGCCGGGTGTGGTGGCAC CCTGGCCATCGTGGCGAAACACCGTCTCTACTGGAAATACAAAAATTAGCCGGGTGTGGTGGCAC T C RNF115 Ensembl:ENSG00000265491 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs781811342 Functional Loss SNV dbSNP153 33..33 33 - - - 20667 RMVar_ID_20667 Human_SNP_ID_32298889 A-to-I Human chr1 - 145794062 145794062 145794062 AGGCAGGCGGATCACTCGAGGTCAGGAGTTCGAGACCAGCCTGGCCATCGTGGCGAAACACCGTC AGGCAGGCGGATCACTCGAGGTCAGGAGTTCGTGACCAGCCTGGCCATCGTGGCGAAACACCGTC T A RNF115 Ensembl:ENSG00000265491 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1172454944 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5683661 20668 RMVar_ID_20668 Human_SNP_ID_32298906 A-to-I Human chr1 - 145794111 145794111 145794111 GGCTGGGCGTGGTGGCTCACGCCTGTAATTCCAGCACTTTGGGAGGCTGAGGCAGGCGGATCACT GGCTGGGCGTGGTGGCTCACGCCTGTAATTCCCGCACTTTGGGAGGCTGAGGCAGGCGGATCACT T G RNF115 Ensembl:ENSG00000265491 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1381944763 Functional Loss SNV dbSNP153 33..33 33 - - - 20669 RMVar_ID_20669 Human_SNP_ID_32309758 A-to-I Human chr1 + 145835017 145835017 145835017 TTTTTTAAAAAATTAGTTGGGTGTGGTGCCATATGCCTGTAGTCACAGCTATTCGAGAGGCTGAG TTTTTTAAAAAATTAGTTGGGTGTGGTGCCATGTGCCTGTAGTCACAGCTATTCGAGAGGCTGAG A G POLR3C Ensembl:ENSG00000186141 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1553728174 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_367263,RMVar_hsa_circ_7733,RMVar_hsa_circ_30243,RMVar_hsa_circ_313335,RMVar_hsa_circ_302935 20670 RMVar_ID_20670 Human_SNP_ID_32309987 A-to-I Human chr1 + 145835754 145835754 145835754 TGCCACCACGCCAGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACTGTGTTGGCCAGGC TGCCACCACGCCAGGCTAATTTTTGTATTTTTCGTAGAGACAGGGTTTCACTGTGTTGGCCAGGC A C POLR3C Ensembl:ENSG00000186141 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs900058524 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_367263,RMVar_hsa_circ_7733,RMVar_hsa_circ_30243,RMVar_hsa_circ_313335,RMVar_hsa_circ_302935 20671 RMVar_ID_20671 Human_SNP_ID_32315706 A-to-I Human chr1 - 145854522 145854522 145854522 TTGTCTGTGTACCTGGTGAGGCAGTTGACTGCAGGAACCCTTCTACAAAAACTCAGAGCAAAGGG TTGTCTGTGTACCTGGTGAGGCAGTTGACTGCGGGAACCCTTCTACAAAAACTCAGAGCAAAGGG T C PIAS3 Ensembl:ENSG00000131788 Protein coding exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1160422862 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_324658 Human_Splice_Rec_118588,Human_Splice_Rec_118589,Human_Splice_Rec_118614,Human_Splice_Rec_118615,Human_Splice_Rec_118648 RMVar_hsa_circ_357974,RMVar_hsa_circ_293311 20672 RMVar_ID_20672 Human_SNP_ID_32330483 A-to-I Human chr1 - 145907843 145907843 145907843 TGGCGTGAACCCAGGGGGGCGGAGCCTGCAGTAAGCCGAGATCACGCCACTGCACTCCAGCCTGG TGGCGTGAACCCAGGGGGGCGGAGCCTGCAGTGAGCCGAGATCACGCCACTGCACTCCAGCCTGG T C ITGA10 Ensembl:ENSG00000143127 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1035121081 Functional Loss SNV dbSNP153 33..33 33 - - - 20673 RMVar_ID_20673 Human_SNP_ID_32332374 A-to-I Human chr1 - 145915096 145915096 145915096 AGTTTTGAGACCAGCCTGACCGGCATGGAGAAACCCCGTCTCTACTAAAAATACAAAATTAGCCG AGTTTTGAGACCAGCCTGACCGGCATGGAGAATCCCCGTCTCTACTAAAAATACAAAATTAGCCG T A PEX11B Ensembl:ENSG00000131779 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs782677508 Functional Loss SNV dbSNP153 33..33 33 - - - 20674 RMVar_ID_20674 Human_SNP_ID_32332375 A-to-I Human chr1 - 145915097 145915097 145915097 GAGTTTTGAGACCAGCCTGACCGGCATGGAGAAACCCCGTCTCTACTAAAAATACAAAATTAGCC GAGTTTTGAGACCAGCCTGACCGGCATGGAGAGACCCCGTCTCTACTAAAAATACAAAATTAGCC T C PEX11B Ensembl:ENSG00000131779 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs587643200 Functional Loss SNV dbSNP153 33..33 33 - - - 20675 RMVar_ID_20675 Human_SNP_ID_32334238 A-to-I Human chr1 - 145921994 145921991 145921995 GTCTTAAACTCCTGACCTCAAGTGATCCACCCACCTTGGCCTTCCAAAATGCTGGGATTACAGGC GTCTTAAACTCCTGACCTCAAGTGATCCACC____TTGGCCTTCCAAAATGCTGGGATTACAGGC AGGTG A RBM8A Ensembl:ENSG00000265241 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1347564029 Functional Loss DEL dbSNP153 32..35 33 - - - 20676 RMVar_ID_20676 Human_SNP_ID_32334250 A-to-I Human chr1 - 145922041 145922041 145922041 TTTTGTATTTTTAGTAGAGATGGGGTTTCGTCATGTTGGCCAGGTTGGTCTTAAACTCCTGACCT TTTTGTATTTTTAGTAGAGATGGGGTTTCGTCGTGTTGGCCAGGTTGGTCTTAAACTCCTGACCT T C RBM8A Ensembl:ENSG00000265241 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs782705107 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9553154 20677 RMVar_ID_20677 Human_SNP_ID_32334273 A-to-I Human chr1 - 145922141 145922141 145922141 TGGCTCACTGCAGCCTCCACTTCCCAGGTTCAAGCAATTCTCGTGCCTCAGCCTCCTGAGTAGTT TGGCTCACTGCAGCCTCCACTTCCCAGGTTCAGGCAATTCTCGTGCCTCAGCCTCCTGAGTAGTT T C RBM8A Ensembl:ENSG00000265241 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs934037700 Functional Loss SNV dbSNP153 33..33 33 - - - 20678 RMVar_ID_20678 Human_SNP_ID_32334504 A-to-I Human chr1 - 145922974 145922974 145922974 GAGCTTGCAGTGAGCAGAGATTGCGCCATTGCACTCCAGCCTGGGCGACAGAGTAAGACTGTCTC GAGCTTGCAGTGAGCAGAGATTGCGCCATTGCGCTCCAGCCTGGGCGACAGAGTAAGACTGTCTC T C RBM8A Ensembl:ENSG00000265241 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355780420 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9553153 20679 RMVar_ID_20679 Human_SNP_ID_32334510 A-to-I Human chr1 - 145923014 145923014 145923014 GGGAGGCTGAGGCAGGAGAATGACCTGAACCCAGGAGGCGGAGCTTGCAGTGAGCAGAGATTGCG GGGAGGCTGAGGCAGGAGAATGACCTGAACCCGGGAGGCGGAGCTTGCAGTGAGCAGAGATTGCG T C RBM8A Ensembl:ENSG00000265241 Protein coding intron GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,29796672,31158229,31158229,31158229 RNA-Seq:(High) rs1444335459 Functional Loss SNV dbSNP153 33..33 33 - - - 20680 RMVar_ID_20680 Human_SNP_ID_32334525 A-to-I Human chr1 - 145923078 145923078 145923078 AAAGATACAAAAAACTAGCCGGGCGTGGTGGTAGGTGCCTGTAGTCCCAGCTACTTGGGAACTCG AAAGATACAAAAAACTAGCCGGGCGTGGTGGTGGGTGCCTGTAGTCCCAGCTACTTGGGAACTCG T C RBM8A Ensembl:ENSG00000265241 Protein coding intron GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,29796672,31158229,31158229,31158229 RNA-Seq:(High) rs782213124 Functional Loss SNV dbSNP153 33..33 33 - - - 20681 RMVar_ID_20681 Human_SNP_ID_32334534 A-to-I Human chr1 - 145923094 145923094 145923094 AAACCCTGTCTGTACTAAAGATACAAAAAACTAGCCGGGCGTGGTGGTAGGTGCCTGTAGTCCCA AAACCCTGTCTGTACTAAAGATACAAAAAACTGGCCGGGCGTGGTGGTAGGTGCCTGTAGTCCCA T C RBM8A Ensembl:ENSG00000265241 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs3199208 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26367427 20682 RMVar_ID_20682 Human_SNP_ID_32334535 A-to-I Human chr1 - 145923101 145923101 145923101 CACAGTGAAACCCTGTCTGTACTAAAGATACAAAAAACTAGCCGGGCGTGGTGGTAGGTGCCTGT CACAGTGAAACCCTGTCTGTACTAAAGATACAGAAAACTAGCCGGGCGTGGTGGTAGGTGCCTGT T C RBM8A Ensembl:ENSG00000265241 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1386863312 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26367427 20683 RMVar_ID_20683 Human_SNP_ID_32334539 A-to-I Human chr1 - 145923108 145923107 145923108 TGGCTAACACAGTGAAACCCTGTCTGTACTAAAGATACAAAAAACTAGCCGGGCGTGGTGGTAGG TGGCTAACACAGTGAAACCCTGTCTGTACTAA_GATACAAAAAACTAGCCGGGCGTGGTGGTAGG CT C RBM8A Ensembl:ENSG00000265241 Protein coding intron GSE100210;GSE99789 HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 29129909,29796672 RNA-Seq:(High) rs1382613436 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_26367427 20684 RMVar_ID_20684 Human_SNP_ID_32334547 A-to-I Human chr1 - 145923130 145923129 145923131 GGTTAGGAGATGGAGACCATCCTGGCTAACACAGTGAAACCCTGTCTGTACTAAAGATACAAAAA GGTTAGGAGATGGAGACCATCCTGGCTAACA__GTGAAACCCTGTCTGTACTAAAGATACAAAAA CTG C RBM8A Ensembl:ENSG00000265241 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1376457441 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_9553152 20685 RMVar_ID_20685 Human_SNP_ID_32335184 A-to-I Human chr1 - 145925600 145925600 145925600 ACTCTATGTATTTCTTTTTTTTCTTTTTTTTGAGATAGAGTCTTGCTGTGTTACCCAGGGTGGAT ACTCTATGTATTTCTTTTTTTTCTTTTTTTTGTGATAGAGTCTTGCTGTGTTACCCAGGGTGGAT T A RBM8A Ensembl:ENSG00000265241 Protein coding intron GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;ASD brains,cerebellum;Bronchiolar epithelium,BEP2D cell line - 29129909,30559470,31158229 RNA-Seq:(High) rs1472700894 Functional Loss SNV dbSNP153 33..33 33 - - - 20686 RMVar_ID_20686 Human_SNP_ID_32337939 A-to-I Human chr1 - 145934932 145934932 145934932 GAACTCCTGACATAAGGTAATCCACCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG GAACTCCTGACATAAGGTAATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG T C LIX1L Ensembl:ENSG00000271601 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1373787035 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_324532,Human_RBP_ID_5683356,Human_RBP_ID_10559045 20687 RMVar_ID_20687 Human_SNP_ID_32340740 A-to-I Human chr1 - 145946295 145946295 145946295 ACTTAGGAGGCTGAGGCAGGAGAATTGCTTGAACTCTGGAGGCGGAGATTGCAGTGATCTGAGAT ACTTAGGAGGCTGAGGCAGGAGAATTGCTTGAGCTCTGGAGGCGGAGATTGCAGTGATCTGAGAT T C LIX1L Ensembl:ENSG00000271601 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1200316790 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16311,RMVar_hsa_circ_284465 20688 RMVar_ID_20688 Human_SNP_ID_32347623 A-to-I Human chr1 + 145975746 145975746 145975746 TAAAATAGAGATAGGGTGTCCTTATGTTGTCCAGGCTGGTCTTGAACTTCTGGGCTCAAGAGATT TAAAATAGAGATAGGGTGTCCTTATGTTGTCCGGGCTGGTCTTGAACTTCTGGGCTCAAGAGATT A G AC243547.3,POLR3GL Ensembl:ENSG00000280778,Ensembl:ENSG00000121851 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1462555681 Functional Loss SNV dbSNP153 33..33 33 - - - 20689 RMVar_ID_20689 Human_SNP_ID_32376370 A-to-I Human chr1 - 146065293 146065293 146065293 GTTTATAGAAGACAGGTCAGCTGTCTGGCTCAATGATCTACATTCTGAAGTTGTCTGAAAATGTC GTTTATAGAAGACAGGTCAGCTGTCTGGCTCAGTGATCTACATTCTGAAGTTGTCTGAAAATGTC T C NBPF10 Ensembl:ENSG00000271425 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs587652722 Functional Loss SNV dbSNP153 33..33 33 - - - 20690 RMVar_ID_20690 Human_SNP_ID_32376371 A-to-I Human chr1 - 146065293 146065293 146065293 GTTTATAGAAGACAGGTCAGCTGTCTGGCTCAATGATCTACATTCTGAAGTTGTCTGAAAATGTC GTTTATAGAAGACAGGTCAGCTGTCTGGCTCACTGATCTACATTCTGAAGTTGTCTGAAAATGTC T G NBPF10 Ensembl:ENSG00000271425 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs587652722 Functional Loss SNV dbSNP153 33..33 33 - - - 20691 RMVar_ID_20691 Human_SNP_ID_32376372 A-to-I Human chr1 - 146065294 146065294 146065294 TGTTTATAGAAGACAGGTCAGCTGTCTGGCTCAATGATCTACATTCTGAAGTTGTCTGAAAATGT TGTTTATAGAAGACAGGTCAGCTGTCTGGCTCCATGATCTACATTCTGAAGTTGTCTGAAAATGT T G NBPF10 Ensembl:ENSG00000271425 Protein coding 3'UTR GSE38233;GSE100210;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 24183664,29129909,30559470 RNA-Seq:(High) rs1434990824 Functional Loss SNV dbSNP153 33..33 33 - - - 20692 RMVar_ID_20692 Human_SNP_ID_32376383 A-to-I Human chr1 - 146065307 146065307 146065307 GGTGACATGGACTTGTTTATAGAAGACAGGTCAGCTGTCTGGCTCAATGATCTACATTCTGAAGT GGTGACATGGACTTGTTTATAGAAGACAGGTCTGCTGTCTGGCTCAATGATCTACATTCTGAAGT T A NBPF10 Ensembl:ENSG00000271425 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1553776734 Functional Loss SNV dbSNP153 33..33 33 - - - 20693 RMVar_ID_20693 Human_SNP_ID_32376765 A-to-I Human chr1 - 146066164 146066164 146066164 CTCTATTCCTATTCTCAAACCATGCCAGTGGCAACCTGTGCGCAGTCTGAAGACAATGGACCCAC CTCTATTCCTATTCTCAAACCATGCCAGTGGCTACCTGTGCGCAGTCTGAAGACAATGGACCCAC T A NBPF10 Ensembl:ENSG00000271425 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1553777095 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10558784 20694 RMVar_ID_20694 Human_SNP_ID_32380411 A-to-I Human chr1 - 146071048 146071048 146071048 TCCAAGTGGCCATTACTGAGCTGAGAGATGTCATTGCCACAGGGAGGACCTATAGGCACATGTAG TCCAAGTGGCCATTACTGAGCTGAGAGATGTCGTTGCCACAGGGAGGACCTATAGGCACATGTAG T C NBPF10 Ensembl:ENSG00000271425 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1553779663 Functional Loss SNV dbSNP153 33..33 33 - - - 20695 RMVar_ID_20695 Human_SNP_ID_32382556 A-to-I Human chr1 - 146081471 146081471 146081471 TCTGAATGTATTGCAGGAATTAAAAAGGACCAAGAAGAGGAAGAAGACCAAGGCCCACCATGCCC TCTGAATGTATTGCAGGAATTAAAAAGGACCAGGAAGAGGAAGAAGACCAAGGCCCACCATGCCC T C NBPF10 Ensembl:ENSG00000271425 Protein coding CDS GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1159226650 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17340295 Human_Splice_Rec_119328,Human_Splice_Rec_119329,Human_Splice_Rec_119504,Human_Splice_Rec_119505 20696 RMVar_ID_20696 Human_SNP_ID_32394079 A-to-I Human chr1 - 146133659 146133659 146133659 GACTCACTGGAGGAATGTGCCATCACTTATTCAAATAGCCATGGCTCTTATGACTCCAACCAGCC GACTCACTGGAGGAATGTGCCATCACTTATTCTAATAGCCATGGCTCTTATGACTCCAACCAGCC T A NBPF10 Ensembl:ENSG00000271425 Protein coding CDS GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs782771842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2091581 Human_Splice_Rec_119208,Human_Splice_Rec_119384,Human_Splice_Rec_119572 20697 RMVar_ID_20697 Human_SNP_ID_32394080 A-to-I Human chr1 - 146133659 146133659 146133659 GACTCACTGGAGGAATGTGCCATCACTTATTCAAATAGCCATGGCTCTTATGACTCCAACCAGCC GACTCACTGGAGGAATGTGCCATCACTTATTCCAATAGCCATGGCTCTTATGACTCCAACCAGCC T G NBPF10 Ensembl:ENSG00000271425 Protein coding CDS GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs782771842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2091581 Human_Splice_Rec_119208,Human_Splice_Rec_119384,Human_Splice_Rec_119572 20698 RMVar_ID_20698 Human_SNP_ID_32553803 A-to-I Human chr1 + 146941359 146941359 146941359 CACCTGCCTCGGCCTCCCAAAGTGTTGGGATTATAGGCATGAGCTACTGCACCCGGCCAGAGTAT CACCTGCCTCGGCCTCCCAAAGTGTTGGGATTGTAGGCATGAGCTACTGCACCCGGCCAGAGTAT A G NBPF12 Ensembl:ENSG00000268043 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1488026061 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10561386 20699 RMVar_ID_20699 Human_SNP_ID_32570391 A-to-I Human chr1 - 146994600 146994600 146994600 CAGGTGCCTATAGGTCCTGCCTGCAGGAATGAAACCTCTCGGCTTAGTAAGGGCTGCTTATTGTG CAGGTGCCTATAGGTCCTGCCTGCAGGAATGACACCTCTCGGCTTAGTAAGGGCTGCTTATTGTG T G - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs12126411 Functional Loss SNV dbSNP153 33..33 33 - - - 20700 RMVar_ID_20700 Human_SNP_ID_32572795 A-to-I Human chr1 - 147000379 147000378 147000379 GTGAGCCCTCATCTCTACTGAAAATCAGAAAAATTATCCGGGTTTGGTGGTGTGAGCCTGTAGTC GTGAGCCCTCATCTCTACTGAAAATCAGAAAA_TTATCCGGGTTTGGTGGTGTGAGCCTGTAGTC AT A HSALNG0006652-001 RNACentral:URS0000E94F94 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1286997427 Functional Loss DEL dbSNP153 33..33 33 - - - 20701 RMVar_ID_20701 Human_SNP_ID_32631856 A-to-I Human chr1 + 147204351 147204351 147204351 CAAACTCTGATGTTATCAACTTTGAAATGGCCAGAATCAGGAAAAATAGATACGCATGCCTGAAC CAAACTCTGATGTTATCAACTTTGAAATGGCCGGAATCAGGAAAAATAGATACGCATGCCTGAAC A G AC242426.2 Ensembl:ENSG00000237188 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879971059 Functional Loss SNV dbSNP153 33..33 33 - - - 20702 RMVar_ID_20702 Human_SNP_ID_32739977 A-to-I Human chr1 + 147583297 147583297 147583297 ATTTATTTATTTATGTATTTTTACTTTTTTTGAGATGGACTCTTGCTCTGTTCCCCAGGCTGGAG ATTTATTTATTTATGTATTTTTACTTTTTTTGCGATGGACTCTTGCTCTGTTCCCCAGGCTGGAG A C BCL9 Ensembl:ENSG00000116128 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335767010 Functional Loss SNV dbSNP153 33..33 33 - - - 20703 RMVar_ID_20703 Human_SNP_ID_32952772 A-to-I Human chr1 - 148448244 148448244 148448244 ATATTTGATATATATAGGTACATATAATATGGATAGATAAATATAGATATATGAGAGAGAAATGG ATATTTGATATATATAGGTACATATAATATGGGTAGATAAATATAGATATATGAGAGAGAAATGG T C LINC01138 Ensembl:ENSG00000274020 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1558299038 Functional Loss SNV dbSNP153 33..33 33 - - - 20704 RMVar_ID_20704 Human_SNP_ID_32979701 A-to-I Human chr1 - 148532133 148532133 148532133 ATATCACCACAAATCACACAACAAAAAGGAGAAGAGATATTTTGGGTTCAAAAAAAGTAAAAAGA ATATCACCACAAATCACACAACAAAAAGGAGAGGAGATATTTTGGGTTCAAAAAAAGTAAAAAGA T C NBPF14 Ensembl:ENSG00000270629 Protein coding 3'UTR GSE100210;GSE112787 HepG2 cell line;293 Flip-In T-REx cells,empty vector - 29129909,29967493 RNA-Seq:(High) rs1395647970 Functional Loss SNV dbSNP153 33..33 33 - - - 20705 RMVar_ID_20705 Human_SNP_ID_32979720 A-to-I Human chr1 - 148532163 148532163 148532163 GACAACTGACCTGTCTCCTTCACATAGTCCATATCACCACAAATCACACAACAAAAAGGAGAAGA GACAACTGACCTGTCTCCTTCACATAGTCCATGTCACCACAAATCACACAACAAAAAGGAGAAGA T C NBPF14 Ensembl:ENSG00000270629 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1337469454 Functional Loss SNV dbSNP153 33..33 33 - - - 20706 RMVar_ID_20706 Human_SNP_ID_33011988 A-to-I Human chr1 + 148798524 148798524 148798524 CCATTTGATGCAGCAATCCCATGATTGGGTACATATCCAGAGGACAATAAATCATTATACCAAAA CCATTTGATGCAGCAATCCCATGATTGGGTACGTATCCAGAGGACAATAAATCATTATACCAAAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1553345102 Functional Loss SNV dbSNP153 33..33 33 - - - 20707 RMVar_ID_20707 Human_SNP_ID_33015203 A-to-I Human chr1 + 148811027 148811027 148811027 ACTGTGTTGCCTAGGTTGGAGTGAAGTGGTGCAATCATAGCTCCCTGCAGTCTCCAACTCCTGGG ACTGTGTTGCCTAGGTTGGAGTGAAGTGGTGCGATCATAGCTCCCTGCAGTCTCCAACTCCTGGG A G PDE4DIP Ensembl:ENSG00000178104 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1553351700 Functional Loss SNV dbSNP153 33..33 33 - - - 20708 RMVar_ID_20708 Human_SNP_ID_33031047 A-to-I Human chr1 + 148863469 148863469 148863469 ACCTCAAACTCCTGGGGTCAAGCTATCCTTTCACCTCAGCCTCCTGAGTAGCTGGGACTATAGAC ACCTCAAACTCCTGGGGTCAAGCTATCCTTTCGCCTCAGCCTCCTGAGTAGCTGGGACTATAGAC A G PDE4DIP Ensembl:ENSG00000178104 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1553403582 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_284088,RMVar_hsa_circ_288192,RMVar_hsa_circ_334657 20709 RMVar_ID_20709 Human_SNP_ID_33037668 A-to-I Human chr1 + 148884581 148884573 148884582 TCAAGCAATCATCATGCCTCAGCCACCTGAGTAGCTGGGACTACAGGCACATGCCACCACGCCCG TCAAGCAATCATCATGCCTCAGCCA_________CTGGGACTACAGGCACATGCCACCACGCCCG ACCTGAGTAG A PDE4DIP Ensembl:ENSG00000178104 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1234211499 Functional Loss DEL dbSNP153 26..34 33 - - - RMVar_hsa_circ_288192,RMVar_hsa_circ_334657,RMVar_hsa_circ_329835,RMVar_hsa_circ_342449 20710 RMVar_ID_20710 Human_SNP_ID_33039912 A-to-I Human chr1 + 148890634 148890634 148890634 AAAAATTAGCGGGTGTGGTGGCATATGCCTGTAGTCCAAGCTACTTGGGAGGCTGAGGCAGGAGA AAAAATTAGCGGGTGTGGTGGCATATGCCTGTTGTCCAAGCTACTTGGGAGGCTGAGGCAGGAGA A T PDE4DIP Ensembl:ENSG00000178104 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1553436143 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_334657,RMVar_hsa_circ_329835,RMVar_hsa_circ_12186,RMVar_hsa_circ_311935 20711 RMVar_ID_20711 Human_SNP_ID_33041890 A-to-I Human chr1 + 148897542 148897541 148897542 GTTGGCGCATGTCAGTAATCCCAGCACTTCGCAAGGCCAAGGTGGGAGGATCACTTGAGCCCAGG GTTGGCGCATGTCAGTAATCCCAGCACTTCGC_AGGCCAAGGTGGGAGGATCACTTGAGCCCAGG CA C PDE4DIP Ensembl:ENSG00000178104 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1285699684 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_334657,RMVar_hsa_circ_329835,RMVar_hsa_circ_12186,RMVar_hsa_circ_311935 20712 RMVar_ID_20712 Human_SNP_ID_33041892 A-to-I Human chr1 + 148897542 148897542 148897542 GTTGGCGCATGTCAGTAATCCCAGCACTTCGCAAGGCCAAGGTGGGAGGATCACTTGAGCCCAGG GTTGGCGCATGTCAGTAATCCCAGCACTTCGCGAGGCCAAGGTGGGAGGATCACTTGAGCCCAGG A G PDE4DIP Ensembl:ENSG00000178104 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1553443304 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_334657,RMVar_hsa_circ_329835,RMVar_hsa_circ_12186,RMVar_hsa_circ_311935 20713 RMVar_ID_20713 Human_SNP_ID_33041901 A-to-I Human chr1 + 148897572 148897570 148897573 GCAAGGCCAAGGTGGGAGGATCACTTGAGCCCAGGAGTTTGAGACCAGCCTGGGAAACATAGCAA GCAAGGCCAAGGTGGGAGGATCACTTGAGCC___GAGTTTGAGACCAGCCTGGGAAACATAGCAA CCAG C PDE4DIP Ensembl:ENSG00000178104 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1296953635 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_334657,RMVar_hsa_circ_329835,RMVar_hsa_circ_12186,RMVar_hsa_circ_311935 20714 RMVar_ID_20714 Human_SNP_ID_33051713 A-to-I Human chr1 + 148935197 148935197 148935197 GATTGCGCCACTGCACTCCAGTCTGGCGACAGAGCAAGACTCCATCTCAAAAAAAAAAAGAATCA GATTGCGCCACTGCACTCCAGTCTGGCGACAGTGCAAGACTCCATCTCAAAAAAAAAAAGAATCA A T PDE4DIP Ensembl:ENSG00000178104 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1298879326 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_304527,RMVar_hsa_circ_334657,RMVar_hsa_circ_311935,RMVar_hsa_circ_49122,RMVar_hsa_circ_327522,RMVar_hsa_circ_288344 20715 RMVar_ID_20715 Human_SNP_ID_33072443 A-to-I Human chr1 + 149005200 149005200 149005200 CTCAGTTACAAGTGATTATTCGTCTAGTCTGGAAAGACCCCGGAAGCTGAGAGCTGTTGGCACCT CTCAGTTACAAGTGATTATTCGTCTAGTCTGGCAAGACCCCGGAAGCTGAGAGCTGTTGGCACCT A C PDE4DIP Ensembl:ENSG00000178104 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs782643474 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18550060 RMVar_hsa_circ_17864,RMVar_hsa_circ_314314 20716 RMVar_ID_20716 Human_SNP_ID_33082542 A-to-I Human chr1 - 149032563 149032563 149032563 GTCACCACATTCATGATGTGAACTCAAAGAACACAGGTGCTACAGTGCAGACCAAGGCCCAGCCT GTCACCACATTCATGATGTGAACTCAAAGAACGCAGGTGCTACAGTGCAGACCAAGGCCCAGCCT T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs782099195 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_98730 Human_miRNA_ID_1736992,Human_miRNA_ID_2889199,Human_miRNA_ID_3096741 20717 RMVar_ID_20717 Human_SNP_ID_33091819 A-to-I Human chr1 - 149054784 149054779 149054784 TTATCACCACAAATCACACAACAAAAAGGAGAAGAGATATTTTGGGTTCAAAAAAAGTAAAAAGA TTATCACCACAAATCACACAACAAAAAGGAGA_____TATTTTGGGTTCAAAAAAAGTAAAAAGA ATCTCT A NBPF9 Ensembl:ENSG00000269713 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1553648326 Functional Loss DEL dbSNP153 33..37 33 - - - 20718 RMVar_ID_20718 Human_SNP_ID_33091823 A-to-I Human chr1 - 149054784 149054783 149054785 TTATCACCACAAATCACACAACAAAAAGGAGAAGAGATATTTTGGGTTCAAAAAAAGTAAAAAGA TTATCACCACAAATCACACAACAAAAAGGAG__GAGATATTTTGGGTTCAAAAAAAGTAAAAAGA CTT C NBPF9 Ensembl:ENSG00000269713 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1429939110 Functional Loss DEL dbSNP153 32..33 33 - - - 20719 RMVar_ID_20719 Human_SNP_ID_33119724 A-to-I Human chr1 - 149122529 149122529 149122529 TTCTCGTTGCCCAGGCTGGAGTGCAGTGACACAATCCCGGCCCACCGCAACCTCCGCCTCCCGGG TTCTCGTTGCCCAGGCTGGAGTGCAGTGACACTATCCCGGCCCACCGCAACCTCCGCCTCCCGGG T A lnc-NBPF9-7,lnc-NBPF9-7:2,lnc-NBPF9-7:3,HSALNG0006646-001 RNACentral:URS0000D5D8A3,RNACentral:URS0000D5DE1C,RNACentral:URS0000D5C9C0,RNACentral:URS0000EA7E67 lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1442520876 Functional Loss SNV dbSNP153 33..33 33 - - - 20720 RMVar_ID_20720 Human_SNP_ID_33140806 A-to-I Human chr1 + 149187650 149187646 149187650 TATTTGATATATATAGGTACATATATATGGATAGATAAATATAGATATATGAGAGAGAAATGGAG TATTTGATATATATAGGTACATATATATG____GATAAATATAGATATATGAGAGAGAAATGGAG GGATA G AC245297.4 Ensembl:ENSG00000274265 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1258601602 Functional Loss DEL dbSNP153 30..33 33 - - - 20721 RMVar_ID_20721 Human_SNP_ID_33204368 A-to-I Human chr1 + 149618916 149618916 149618916 TTTGATATATATAGGTACATATATATGGATAGATAAATATAGATATATGAGAGAGAAATGGAGAT TTTGATATATATAGGTACATATATATGGATAGGTAAATATAGATATATGAGAGAGAAATGGAGAT A G LINC00869 Ensembl:ENSG00000277147 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1295893286 Functional Loss SNV dbSNP153 33..33 33 - - - 20722 RMVar_ID_20722 Human_SNP_ID_33204369 A-to-I Human chr1 + 149618916 149618916 149618916 TTTGATATATATAGGTACATATATATGGATAGATAAATATAGATATATGAGAGAGAAATGGAGAT TTTGATATATATAGGTACATATATATGGATAGTTAAATATAGATATATGAGAGAGAAATGGAGAT A T LINC00869 Ensembl:ENSG00000277147 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1295893286 Functional Loss SNV dbSNP153 33..33 33 - - - 20723 RMVar_ID_20723 Human_SNP_ID_33267723 A-to-I Human chr1 + 149887575 149887575 149887575 TTGTGACTCTCCGTTTTCTTGGGCAACAGGACAGCCTGGATATTGGGCAAGACGCCGCCCTGGGC TTGTGACTCTCCGTTTTCTTGGGCAACAGGACGGCCTGGATATTGGGCAAGACGCCGCCCTGGGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1553760067 Functional Loss SNV dbSNP153 33..33 33 - - - 20724 RMVar_ID_20724 Human_SNP_ID_33267728 A-to-I Human chr1 + 149887584 149887584 149887584 TCCGTTTTCTTGGGCAACAGGACAGCCTGGATATTGGGCAAGACGCCGCCCTGGGCAATGGTGAC TCCGTTTTCTTGGGCAACAGGACAGCCTGGATGTTGGGCAAGACGCCGCCCTGGGCAATGGTGAC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1553760072 Functional Loss SNV dbSNP153 33..33 33 - - - 20725 RMVar_ID_20725 Human_SNP_ID_33267732 A-to-I Human chr1 + 149887591 149887591 149887591 TCTTGGGCAACAGGACAGCCTGGATATTGGGCAAGACGCCGCCCTGGGCAATGGTGACACCCCCG TCTTGGGCAACAGGACAGCCTGGATATTGGGCGAGACGCCGCCCTGGGCAATGGTGACACCCCCG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs377603650 Functional Loss SNV dbSNP153 33..33 33 - - - 20726 RMVar_ID_20726 Human_SNP_ID_33267761 A-to-I Human chr1 - 149887662 149887662 149887662 AAGAAGACGCGCATCATCCCTCGCCATCTGCAACTAGCCGTGAGGAATGACGAAGAGCTCAACAA AAGAAGACGCGCATCATCCCTCGCCATCTGCAGCTAGCCGTGAGGAATGACGAAGAGCTCAACAA T C H2AC21 Ensembl:ENSG00000184270 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs782219439 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1411090,Human_RBP_ID_1724787,Human_RBP_ID_3990983,Human_RBP_ID_18550716 20727 RMVar_ID_20727 Human_SNP_ID_33267765 A-to-I Human chr1 - 149887690 149887687 149887690 GCTGGCGGGCAACGCGGCTCGGGACAACAAGAAGACGCGCATCATCCCTCGCCATCTGCAACTAG GCTGGCGGGCAACGCGGCTCGGGACAACAAGA___CGCGCATCATCCCTCGCCATCTGCAACTAG GTCT G H2AC21 Ensembl:ENSG00000184270 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs782564731 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_3990990,Human_RBP_ID_26389721,Human_RBP_ID_27387518 20728 RMVar_ID_20728 Human_SNP_ID_33267825 A-to-I Human chr1 + 149887799 149887799 149887799 CACCGGGGCGCCTGCCCCGACCCGCTCCGCGTAGTTGCCTTTGCGCAGCAAGCGGTGCACTCGCC CACCGGGGCGCCTGCCCCGACCCGCTCCGCGTGGTTGCCTTTGCGCAGCAAGCGGTGCACTCGCC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1553760150 Functional Loss SNV dbSNP153 33..33 33 - - - 20729 RMVar_ID_20729 Human_SNP_ID_33268331 A-to-I Human chr1 + 149889417 149889417 149889417 TTCCTCTGTCACCCAGGCTGGAGCACTATCTCAGCTCACTGCAACCTCCACCACCGCCTCCTCCA TTCCTCTGTCACCCAGGCTGGAGCACTATCTCGGCTCACTGCAACCTCCACCACCGCCTCCTCCA A G BOLA1 Ensembl:ENSG00000178096 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs993772413 Functional Loss SNV dbSNP153 33..33 33 - - - 20730 RMVar_ID_20730 Human_SNP_ID_33272175 A-to-I Human chr1 - 149905003 149905003 149905003 CCGGGGGCAGGTGCTGCAGTGAAGGGGTCTCTAGGGCTTTGGGATTGGCAGGCACACTGTGAGAC CCGGGGGCAGGTGCTGCAGTGAAGGGGTCTCTGGGGCTTTGGGATTGGCAGGCACACTGTGAGAC T C SV2A Ensembl:ENSG00000159164 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1553762462 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224314,Human_RBP_ID_325148,Human_RBP_ID_3280358,Human_RBP_ID_5685350,Human_RBP_ID_18929923 20731 RMVar_ID_20731 Human_SNP_ID_33276969 A-to-I Human chr1 - 149923482 149923482 149923482 TTTTCCCAATATCTTTTCTATTCCTTGGACCAATCAGAGATGCTGTAGCTCCTTGGGGCAAAGGT TTTTCCCAATATCTTTTCTATTCCTTGGACCAGTCAGAGATGCTGTAGCTCCTTGGGGCAAAGGT T C SF3B4 Ensembl:ENSG00000143368 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs587610611 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_325153,Human_RBP_ID_970850,Human_RBP_ID_1411108,Human_RBP_ID_1724801,Human_RBP_ID_5685371,Human_RBP_ID_8955614,Human_RBP_ID_10565470,Human_RBP_ID_17212070,Human_RBP_ID_17329988,Human_RBP_ID_17445797,Human_RBP_ID_17647046,Human_RBP_ID_17724683,Human_RBP_ID_19186392,Human_RBP_ID_22779770,Human_RBP_ID_23260280,Human_RBP_ID_23330312,Human_RBP_ID_24398801,Human_RBP_ID_24447022,Human_RBP_ID_27578368 Human_miRNA_ID_244879,Human_miRNA_ID_247382,Human_miRNA_ID_1503641 20732 RMVar_ID_20732 Human_SNP_ID_33276970 A-to-I Human chr1 - 149923482 149923482 149923482 TTTTCCCAATATCTTTTCTATTCCTTGGACCAATCAGAGATGCTGTAGCTCCTTGGGGCAAAGGT TTTTCCCAATATCTTTTCTATTCCTTGGACCACTCAGAGATGCTGTAGCTCCTTGGGGCAAAGGT T G SF3B4 Ensembl:ENSG00000143368 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs587610611 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_325153,Human_RBP_ID_970850,Human_RBP_ID_1411108,Human_RBP_ID_1724801,Human_RBP_ID_5685371,Human_RBP_ID_8955614,Human_RBP_ID_10565470,Human_RBP_ID_17212070,Human_RBP_ID_17329988,Human_RBP_ID_17445797,Human_RBP_ID_17647046,Human_RBP_ID_17724683,Human_RBP_ID_19186392,Human_RBP_ID_22779770,Human_RBP_ID_23260280,Human_RBP_ID_23330312,Human_RBP_ID_24398801,Human_RBP_ID_24447022,Human_RBP_ID_27578368 Human_miRNA_ID_244879,Human_miRNA_ID_247382,Human_miRNA_ID_1503641 20733 RMVar_ID_20733 Human_SNP_ID_33278174 A-to-I Human chr1 - 149927723 149927723 149927723 CTGCCGGGCCGATCTCCGAGCGGAATCAGGGTAACTGGAGGGGGAAAGTCTGGAATGGGCTCAGC CTGCCGGGCCGATCTCCGAGCGGAATCAGGGTGACTGGAGGGGGAAAGTCTGGAATGGGCTCAGC T C SF3B4 Ensembl:ENSG00000143368 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1278642185 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_222178,Human_RBP_ID_850342,Human_RBP_ID_4075903,Human_RBP_ID_5335799,Human_RBP_ID_19039031,Human_RBP_ID_22871832,Human_RBP_ID_26311727 RMVar_hsa_circ_135861,RMVar_hsa_circ_107192 20734 RMVar_ID_20734 Human_SNP_ID_33282263 A-to-I Human chr1 - 149941821 149941821 149941821 AGCACTCCCCTAAGTTGCAAAATTTAAGGGTTACTATAAAACTCATTAATCAAGATACTATAAAA AGCACTCCCCTAAGTTGCAAAATTTAAGGGTTGCTATAAAACTCATTAATCAAGATACTATAAAA T C OTUD7B Ensembl:ENSG00000264522 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1319840262 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_970866,Human_RBP_ID_5685491,Human_RBP_ID_8955618,Human_RBP_ID_16969878,Human_RBP_ID_17724727,Human_RBP_ID_18216500,Human_RBP_ID_27578391 20735 RMVar_ID_20735 Human_SNP_ID_33282265 A-to-I Human chr1 - 149941827 149941827 149941827 GAGATGAGCACTCCCCTAAGTTGCAAAATTTAAGGGTTACTATAAAACTCATTAATCAAGATACT GAGATGAGCACTCCCCTAAGTTGCAAAATTTAGGGGTTACTATAAAACTCATTAATCAAGATACT T C OTUD7B Ensembl:ENSG00000264522 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1393336521 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27578392 20736 RMVar_ID_20736 Human_SNP_ID_33282266 A-to-I Human chr1 - 149941833 149941833 149941833 TGGTATGAGATGAGCACTCCCCTAAGTTGCAAAATTTAAGGGTTACTATAAAACTCATTAATCAA TGGTATGAGATGAGCACTCCCCTAAGTTGCAACATTTAAGGGTTACTATAAAACTCATTAATCAA T G OTUD7B Ensembl:ENSG00000264522 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1323273409 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27578392 20737 RMVar_ID_20737 Human_SNP_ID_33286871 A-to-I Human chr1 - 149959338 149959338 149959338 TATCAGGCCGGGTGTGGTGTCTCACACCTGTAATCTCAGCACTTTGAAAGGCTGAGGCAGGAGGA TATCAGGCCGGGTGTGGTGTCTCACACCTGTAGTCTCAGCACTTTGAAAGGCTGAGGCAGGAGGA T C OTUD7B Ensembl:ENSG00000264522 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1301764427 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8598 20738 RMVar_ID_20738 Human_SNP_ID_233831841 A-to-I Human chr5 - 60605837 60605837 60605837 TTTTCTAAATCAGGTTTGTTACAGAAGGAGAAAGTGGCAGTTGAAGCATTTCAGATTTGCTGCCT TTTTCTAAATCAGGTTTGTTACAGAAGGAGAATGTGGCAGTTGAAGCATTTCAGATTTGCTGCCT T A DEPDC1B Ensembl:ENSG00000035499 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1356333285 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_654082,Human_Splice_Rec_654102,Human_Splice_Rec_654122,Human_Splice_Rec_654128 Human_miRNA_ID_1379576 RMVar_hsa_circ_1770,RMVar_hsa_circ_124285,RMVar_hsa_circ_231609,RMVar_hsa_circ_231608,RMVar_hsa_circ_305097,RMVar_hsa_circ_358689,RMVar_hsa_circ_40647,RMVar_hsa_circ_231610,RMVar_hsa_circ_108526 20739 RMVar_ID_20739 Human_SNP_ID_233866916 A-to-I Human chr5 - 60754151 60754151 60754151 TTGTCATTTATTGACTGTATTCAGAAGATACTATATTTGCTCTAGAGTTAACTCCCATTTTAGCA TTGTCATTTATTGACTGTATTCAGAAGATACTGTATTTGCTCTAGAGTTAACTCCCATTTTAGCA T C ELOVL7 Ensembl:ENSG00000164181 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs901622364 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_643879,Human_RBP_ID_7452333,Human_RBP_ID_17530558,Human_RBP_ID_27741831 Human_miRNA_ID_154039,Human_miRNA_ID_646357,Human_miRNA_ID_2797464,Human_miRNA_ID_2798430,Human_miRNA_ID_2799811,Human_miRNA_ID_2807126,Human_miRNA_ID_2810270,Human_miRNA_ID_2813412,Human_miRNA_ID_2833002,Human_miRNA_ID_2852525,Human_miRNA_ID_2853587,Human_miRNA_ID_2860669 RMVar_hsa_circ_231616,RMVar_hsa_circ_231617,RMVar_hsa_circ_231618,RMVar_hsa_circ_231619,RMVar_hsa_circ_116106 20740 RMVar_ID_20740 Human_SNP_ID_233893134 A-to-I Human chr5 - 60866977 60866977 60866977 AAAAAAAAAATTAGGCGGGCACTTGTAGTCCCAGCTATTTGGGAGGCTGAGGCAGGAGAATGGCG AAAAAAAAAATTAGGCGGGCACTTGTAGTCCCGGCTATTTGGGAGGCTGAGGCAGGAGAATGGCG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs958360790 Functional Loss SNV dbSNP153 33..33 33 - - - 20741 RMVar_ID_20741 Human_SNP_ID_233898214 A-to-I Human chr5 - 60885067 60885067 60885067 TCAAGGCTACAGTGAGCCACAATTGCACCACTATACTCCAGCCTGGGTGACAGAGTGAGATCTTG TCAAGGCTACAGTGAGCCACAATTGCACCACTGTACTCCAGCCTGGGTGACAGAGTGAGATCTTG T C ERCC8 Ensembl:ENSG00000049167 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1015340612 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25905094 RMVar_hsa_circ_231621,RMVar_hsa_circ_77523 20742 RMVar_ID_20742 Human_SNP_ID_233898230 A-to-I Human chr5 - 60885135 60885135 60885135 GGTGGCTTTACACTTATAGTTCCAGCTACTTAAGAGGGTGAGGTGGGAGGATCACTGAGCCCAAG GGTGGCTTTACACTTATAGTTCCAGCTACTTAGGAGGGTGAGGTGGGAGGATCACTGAGCCCAAG T C ERCC8 Ensembl:ENSG00000049167 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs993906832 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_231621,RMVar_hsa_circ_77523 20743 RMVar_ID_20743 Human_SNP_ID_233913014 A-to-I Human chr5 + 60945350 60945350 60945350 GCACGTGGGCACGGACCAATTCGGGAACAAATACTACTACATCCCGCAGTACAAGAACTGGAGAG GCACGTGGGCACGGACCAATTCGGGAACAAATGCTACTACATCCCGCAGTACAAGAACTGGAGAG A G NDUFAF2 Ensembl:ENSG00000164182 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs755836979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_643951,Human_RBP_ID_1997017,Human_RBP_ID_5427403,Human_RBP_ID_18050125,Human_RBP_ID_18448906,Human_RBP_ID_23291825,Human_RBP_ID_24110367,Human_RBP_ID_27516630 Human_Splice_Rec_654435,Human_Splice_Rec_654441,Human_Splice_Rec_654445 20744 RMVar_ID_20744 Human_SNP_ID_233923351 A-to-I Human chr5 + 60987266 60987266 60987266 TTGAATCCCTGAACAGACCGATAATGAGCTCTAAAACTGAATCAGTAATAAATAGCCTACCAATC TTGAATCCCTGAACAGACCGATAATGAGCTCTGAAACTGAATCAGTAATAAATAGCCTACCAATC A G NDUFAF2 Ensembl:ENSG00000164182 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1249746108 Functional Loss SNV dbSNP153 33..33 33 - - - 20745 RMVar_ID_20745 Human_SNP_ID_233961704 A-to-I Human chr5 - 61156374 61156363 61156375 TCGCTATGTTGCCCAGGCTGGTCTCAAATGCCAGGCCTCAAGCAATCCTCCCATCTTTGCCTCCC TCGCTATGTTGCCCAGGCTGGTCTCAAATGC____________AATCCTCCCATCTTTGCCTCCC TGCTTGAGGCCTG T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1414157101 Functional Loss DEL dbSNP153 32..43 33 - - - 20746 RMVar_ID_20746 Human_SNP_ID_233961706 A-to-I Human chr5 - 61156366 61156366 61156366 TTGCCCAGGCTGGTCTCAAATGCCAGGCCTCAAGCAATCCTCCCATCTTTGCCTCCCAAAGCACT TTGCCCAGGCTGGTCTCAAATGCCAGGCCTCAGGCAATCCTCCCATCTTTGCCTCCCAAAGCACT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893982183 Functional Loss SNV dbSNP153 33..33 33 - - - 20747 RMVar_ID_20747 Human_SNP_ID_233961827 A-to-I Human chr5 - 61156854 61156854 61156854 TTTTTTAAGAGACAGAGTCATGCTCTGTCACCAGGCTGGAGTACAGTGGCCTGATGATAGTTCAC TTTTTTAAGAGACAGAGTCATGCTCTGTCACCGGGCTGGAGTACAGTGGCCTGATGATAGTTCAC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1212921720 Functional Loss SNV dbSNP153 33..33 33 - - - 20748 RMVar_ID_20748 Human_SNP_ID_234015017 A-to-I Human chr5 + 61365935 61365935 61365935 AAATGTATCGTCTATCAGGTGTCTTTTTTTTTAAGATGGTCTCATTCTGTCACCCAGGCTGGCAG AAATGTATCGTCTATCAGGTGTCTTTTTTTTTGAGATGGTCTCATTCTGTCACCCAGGCTGGCAG A G ZSWIM6 Ensembl:ENSG00000130449 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025940547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15477971 RMVar_hsa_circ_231636,RMVar_hsa_circ_89533 20749 RMVar_ID_20749 Human_SNP_ID_234015028 A-to-I Human chr5 + 61365985 61365985 61365985 CACCCAGGCTGGCAGTGATTTTGGCTCACTGCAACCTCCACCTCCCAGGCTCAAGTGATCCTCCC CACCCAGGCTGGCAGTGATTTTGGCTCACTGCGACCTCCACCTCCCAGGCTCAAGTGATCCTCCC A G ZSWIM6 Ensembl:ENSG00000130449 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264757620 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_231636,RMVar_hsa_circ_89533 20750 RMVar_ID_20750 Human_SNP_ID_234015236 A-to-I Human chr5 + 61366786 61366786 61366786 ACCCCATCTCCACAAAAATACAAAAATTAACCAGACGTGATGGCGCACACCTGTAGTCCCAGCTA ACCCCATCTCCACAAAAATACAAAAATTAACCCGACGTGATGGCGCACACCTGTAGTCCCAGCTA A C ZSWIM6 Ensembl:ENSG00000130449 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1473876264 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_231636,RMVar_hsa_circ_89533 20751 RMVar_ID_20751 Human_SNP_ID_234015549 A-to-I Human chr5 + 61368071 61368071 61368071 ATCACTTGATGCCAAAAGGTCGAGACTGTAGTAAGCAGTGATAATGCCACTGTACTCCAGCCTGG ATCACTTGATGCCAAAAGGTCGAGACTGTAGTGAGCAGTGATAATGCCACTGTACTCCAGCCTGG A G ZSWIM6 Ensembl:ENSG00000130449 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs967542100 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_231636,RMVar_hsa_circ_89533 20752 RMVar_ID_20752 Human_SNP_ID_234017342 A-to-I Human chr5 + 61375503 61375502 61375504 TTCTGAAGATGAGGATAAGAAACAAGGAAAACAGAGAAAGAAAAAGAAGAACCGTTCACATAAAT TTCTGAAGATGAGGATAAGAAACAAGGAAAAC__AGAAAGAAAAAGAAGAACCGTTCACATAAAT CAG C ZSWIM6,AC122718.1 Ensembl:ENSG00000130449,Ensembl:ENSG00000250461 Protein coding,Pseudogene intron,exon GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs532201750 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_5103405,Human_RBP_ID_18538420 RMVar_hsa_circ_231636,RMVar_hsa_circ_89533 20753 RMVar_ID_20753 Human_SNP_ID_234018178 A-to-I Human chr5 + 61379058 61379058 61379058 AAAAAATTAGCTGGGTGTCGTGGTGCGTGCCTATAATCCTAGCTACTCAGGTGGCGGAGGTGAGA AAAAAATTAGCTGGGTGTCGTGGTGCGTGCCTGTAATCCTAGCTACTCAGGTGGCGGAGGTGAGA A G ZSWIM6 Ensembl:ENSG00000130449 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984049852 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25905758 RMVar_hsa_circ_231636,RMVar_hsa_circ_89533 20754 RMVar_ID_20754 Human_SNP_ID_234019634 A-to-I Human chr5 + 61384796 61384796 61384796 AATCTTGGAGGAGGCCGGGCGCGGTGGGTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGC AATCTTGGAGGAGGCCGGGCGCGGTGGGTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGC A G ZSWIM6 Ensembl:ENSG00000130449 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1298446599 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_231636,RMVar_hsa_circ_89533 20755 RMVar_ID_20755 Human_SNP_ID_234021680 A-to-I Human chr5 + 61393623 61393623 61393623 GGCCGGGCGTGGTGGCGCATGTCTGTAATCCCAGCTGCTCAGGATGCTGAGGCAGGAGAATCACT GGCCGGGCGTGGTGGCGCATGTCTGTAATCCCCGCTGCTCAGGATGCTGAGGCAGGAGAATCACT A C ZSWIM6 Ensembl:ENSG00000130449 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs990680311 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15478400 RMVar_hsa_circ_231636,RMVar_hsa_circ_89533 20756 RMVar_ID_20756 Human_SNP_ID_234036374 A-to-I Human chr5 + 61457625 61457624 61457625 CTCACTACATCCTCTGCCTCCCAGGTTCAAGCAATTCTCCTGCCTTAGCCTCCTGAGTAGCTGGG CTCACTACATCCTCTGCCTCCCAGGTTCAAGC_ATTCTCCTGCCTTAGCCTCCTGAGTAGCTGGG CA C ZSWIM6 Ensembl:ENSG00000130449 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1238800388 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_25906066 RMVar_hsa_circ_231636,RMVar_hsa_circ_89533,RMVar_hsa_circ_231638 20757 RMVar_ID_20757 Human_SNP_ID_234036397 A-to-I Human chr5 + 61457732 61457732 61457732 TTTAGTAGAGATGGGGTTTCACCATGTTGGCCAAGCTGGTCTCGAACTTCTGACCTCAGGTGATC TTTAGTAGAGATGGGGTTTCACCATGTTGGCCGAGCTGGTCTCGAACTTCTGACCTCAGGTGATC A G ZSWIM6 Ensembl:ENSG00000130449 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs952160935 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_231636,RMVar_hsa_circ_89533,RMVar_hsa_circ_231638 20758 RMVar_ID_20758 Human_SNP_ID_234240972 A-to-I Human chr5 + 62322182 62322182 62322182 AGACTCCTGGGCTCAAGTGATCCTCCCGTCTCAGCCTCTCAGAAGTGCTGGGATGACAGGTATGA AGACTCCTGGGCTCAAGTGATCCTCCCGTCTCCGCCTCTCAGAAGTGCTGGGATGACAGGTATGA A C KIF2A Ensembl:ENSG00000068796 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1196030791 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4739,RMVar_hsa_circ_114034,RMVar_hsa_circ_39676,RMVar_hsa_circ_231655 20759 RMVar_ID_20759 Human_SNP_ID_234244640 A-to-I Human chr5 + 62337371 62337371 62337371 AAAATTAGCAAGGTGTGGTGGCGCGTGCATGTAATCCCAGCTATTCAGGAGGCTGAGGCAGGAGA AAAATTAGCAAGGTGTGGTGGCGCGTGCATGTCATCCCAGCTATTCAGGAGGCTGAGGCAGGAGA A C KIF2A Ensembl:ENSG00000068796 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1413118979 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4739,RMVar_hsa_circ_114034,RMVar_hsa_circ_39676,RMVar_hsa_circ_231655 20760 RMVar_ID_20760 Human_SNP_ID_234247774 A-to-I Human chr5 + 62350443 62350443 62350443 GGGACCACAGGCATGAGCCACTATGCCCAGCTAATTTTTTGATTTTTTAGTAGAGAGTCTTTCCA GGGACCACAGGCATGAGCCACTATGCCCAGCTGATTTTTTGATTTTTTAGTAGAGAGTCTTTCCA A G KIF2A Ensembl:ENSG00000068796 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1561267138 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114034,RMVar_hsa_circ_39676,RMVar_hsa_circ_30148,RMVar_hsa_circ_231663,RMVar_hsa_circ_317859,RMVar_hsa_circ_340357,RMVar_hsa_circ_231655,RMVar_hsa_circ_356848,RMVar_hsa_circ_322280,RMVar_hsa_circ_324674,RMVar_hsa_circ_319503,RMVar_hsa_circ_306321,RMVar_hsa_circ_310914,RMVar_hsa_circ_273102,RMVar_hsa_circ_16350,RMVar_hsa_circ_37254,RMVar_hsa_circ_231664,RMVar_hsa_circ_231665,RMVar_hsa_circ_231659,RMVar_hsa_circ_231661,RMVar_hsa_circ_231662,RMVar_hsa_circ_231660,RMVar_hsa_circ_339608,RMVar_hsa_circ_45721,RMVar_hsa_circ_3578,RMVar_hsa_circ_17948,RMVar_hsa_circ_231667 20761 RMVar_ID_20761 Human_SNP_ID_234252450 A-to-I Human chr5 + 62370998 62370998 62370998 TAGAAATTTAGATTTTTCAGGCCAGACGCTGTAGCTCATGCTTGTAATCCCAGTACTTTGGGAGG TAGAAATTTAGATTTTTCAGGCCAGACGCTGTCGCTCATGCTTGTAATCCCAGTACTTTGGGAGG A C KIF2A Ensembl:ENSG00000068796 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs570855401 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15480526 RMVar_hsa_circ_114034,RMVar_hsa_circ_317859,RMVar_hsa_circ_231655,RMVar_hsa_circ_356848,RMVar_hsa_circ_273102,RMVar_hsa_circ_231664,RMVar_hsa_circ_231665,RMVar_hsa_circ_45721,RMVar_hsa_circ_231675,RMVar_hsa_circ_30910,RMVar_hsa_circ_332262,RMVar_hsa_circ_56406,RMVar_hsa_circ_231681,RMVar_hsa_circ_37378,RMVar_hsa_circ_285783,RMVar_hsa_circ_231687,RMVar_hsa_circ_35471,RMVar_hsa_circ_231690,RMVar_hsa_circ_376665,RMVar_hsa_circ_284121 20762 RMVar_ID_20762 Human_SNP_ID_234254411 A-to-I Human chr5 + 62380067 62380067 62380067 GCGTGTGCCATCACGCCTGGCTAATTTTTTGTATTTTTAGAAGAGACAGGGTTTCACCATGTTGG GCGTGTGCCATCACGCCTGGCTAATTTTTTGTGTTTTTAGAAGAGACAGGGTTTCACCATGTTGG A G KIF2A Ensembl:ENSG00000068796 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1001657039 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_317859,RMVar_hsa_circ_231665,RMVar_hsa_circ_45721,RMVar_hsa_circ_231675,RMVar_hsa_circ_332262,RMVar_hsa_circ_37378,RMVar_hsa_circ_231696,RMVar_hsa_circ_376665,RMVar_hsa_circ_231694,RMVar_hsa_circ_326393,RMVar_hsa_circ_266211,RMVar_hsa_circ_231693,RMVar_hsa_circ_348312,RMVar_hsa_circ_339878,RMVar_hsa_circ_231695 20763 RMVar_ID_20763 Human_SNP_ID_234268100 A-to-I Human chr5 + 62431476 62431476 62431476 CAGTGGGGTGATCTCAGCTCACTGTAGCCTCTACCTCCTGAGTTCAAGCGATTTTTCCAGGGGCT CAGTGGGGTGATCTCAGCTCACTGTAGCCTCTGCCTCCTGAGTTCAAGCGATTTTTCCAGGGGCT A G KIF2A,IPO11 Ensembl:ENSG00000068796,Ensembl:ENSG00000086200 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1261205202 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_231705,RMVar_hsa_circ_109617 20764 RMVar_ID_20764 Human_SNP_ID_234275888 A-to-I Human chr5 + 62458466 62458466 62458466 GGGATTACAGGTGCATGCCGCTATGCCCGGCTAATTTTTGTACTTTTAGTAGGGACAGGGTTTTG GGGATTACAGGTGCATGCCGCTATGCCCGGCTGATTTTTGTACTTTTAGTAGGGACAGGGTTTTG A G KIF2A,IPO11 Ensembl:ENSG00000068796,Ensembl:ENSG00000086200 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs572482181 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55049,RMVar_hsa_circ_14767,RMVar_hsa_circ_231705,RMVar_hsa_circ_109617,RMVar_hsa_circ_314332,RMVar_hsa_circ_346914,RMVar_hsa_circ_352536,RMVar_hsa_circ_355673,RMVar_hsa_circ_369990,RMVar_hsa_circ_352904,RMVar_hsa_circ_347189,RMVar_hsa_circ_338140,RMVar_hsa_circ_43291,RMVar_hsa_circ_34263,RMVar_hsa_circ_86608,RMVar_hsa_circ_120381,RMVar_hsa_circ_231707,RMVar_hsa_circ_231708,RMVar_hsa_circ_231706,RMVar_hsa_circ_372137,RMVar_hsa_circ_231710,RMVar_hsa_circ_379039,RMVar_hsa_circ_358307,RMVar_hsa_circ_115753,RMVar_hsa_circ_120003,RMVar_hsa_circ_104093,RMVar_hsa_circ_85156,RMVar_hsa_circ_56357,RMVar_hsa_circ_114373,RMVar_hsa_circ_231714,RMVar_hsa_circ_231718,RMVar_hsa_circ_51218,RMVar_hsa_circ_54837,RMVar_hsa_circ_2683,RMVar_hsa_circ_231719,RMVar_hsa_circ_231716,RMVar_hsa_circ_231717,RMVar_hsa_circ_231715,RMVar_hsa_circ_231713,RMVar_hsa_circ_104171,RMVar_hsa_circ_231721,RMVar_hsa_circ_55906,RMVar_hsa_circ_231722 20765 RMVar_ID_20765 Human_SNP_ID_234286670 A-to-I Human chr5 + 62500162 62500162 62500162 CAAAAATTAGCCAGACATGGTGGCATGTGCCTATAGTCCCAGCTACTCGGGAGGCTGAGGTGGGA CAAAAATTAGCCAGACATGGTGGCATGTGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGTGGGA A G KIF2A,IPO11 Ensembl:ENSG00000068796,Ensembl:ENSG00000086200 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1013723419 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_825,RMVar_hsa_circ_55049,RMVar_hsa_circ_231705,RMVar_hsa_circ_109617,RMVar_hsa_circ_314332,RMVar_hsa_circ_352536,RMVar_hsa_circ_355673,RMVar_hsa_circ_347189,RMVar_hsa_circ_338140,RMVar_hsa_circ_43291,RMVar_hsa_circ_34263,RMVar_hsa_circ_86608,RMVar_hsa_circ_120381,RMVar_hsa_circ_231707,RMVar_hsa_circ_231706,RMVar_hsa_circ_372137,RMVar_hsa_circ_231710,RMVar_hsa_circ_115753,RMVar_hsa_circ_120003,RMVar_hsa_circ_104093,RMVar_hsa_circ_56357,RMVar_hsa_circ_114373,RMVar_hsa_circ_231718,RMVar_hsa_circ_51218,RMVar_hsa_circ_2683,RMVar_hsa_circ_231719,RMVar_hsa_circ_231716,RMVar_hsa_circ_231717,RMVar_hsa_circ_231715,RMVar_hsa_circ_57355,RMVar_hsa_circ_104171,RMVar_hsa_circ_231721,RMVar_hsa_circ_231722,RMVar_hsa_circ_35908,RMVar_hsa_circ_124640,RMVar_hsa_circ_231723,RMVar_hsa_circ_374587,RMVar_hsa_circ_358379,RMVar_hsa_circ_231725,RMVar_hsa_circ_304484,RMVar_hsa_circ_20651,RMVar_hsa_circ_5779,RMVar_hsa_circ_231728,RMVar_hsa_circ_271602,RMVar_hsa_circ_324036,RMVar_hsa_circ_363147,RMVar_hsa_circ_333248,RMVar_hsa_circ_275976,RMVar_hsa_circ_40241,RMVar_hsa_circ_17817,RMVar_hsa_circ_231731,RMVar_hsa_circ_231732,RMVar_hsa_circ_231730,RMVar_hsa_circ_353370,RMVar_hsa_circ_374282,RMVar_hsa_circ_231734,RMVar_hsa_circ_231735,RMVar_hsa_circ_341014,RMVar_hsa_circ_70263,RMVar_hsa_circ_119015,RMVar_hsa_circ_270093,RMVar_hsa_circ_231737,RMVar_hsa_circ_231742,RMVar_hsa_circ_113150,RMVar_hsa_circ_342843,RMVar_hsa_circ_231743 20766 RMVar_ID_20766 Human_SNP_ID_234320529 A-to-I Human chr5 - 62628384 62628384 62628384 CTTGCTTTTGAGTATTTCCTAAAAAATGCTTTAAAGTTTCCTTACAATAAATGGCAAGTAAAACA CTTGCTTTTGAGTATTTCCTAAAAAATGCTTTGAAGTTTCCTTACAATAAATGGCAAGTAAAACA T C RF00017-4575,RF00017-4596 RNACentral:URS0000918622,RNACentral:URS00009759B0 SRP RNA,SRP RNA intron,intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs771515847 Functional Loss SNV dbSNP153 33..33 33 - - - 20767 RMVar_ID_20767 Human_SNP_ID_234842918 A-to-I Human chr5 - 64721290 64721290 64721290 ATTGAGTACCTAACGTGGCAAACGCTGTGCTAAGTACTGGGGATACAGAGATAAGTAAGACACAT ATTGAGTACCTAACGTGGCAAACGCTGTGCTAGGTACTGGGGATACAGAGATAAGTAAGACACAT T C SREK1IP1 Ensembl:ENSG00000153006 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1485640545 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7456419,Human_RBP_ID_8891118,Human_RBP_ID_15485036,Human_RBP_ID_27742214 RMVar_hsa_circ_102165,RMVar_hsa_circ_231770 20768 RMVar_ID_20768 Human_SNP_ID_234873332 A-to-I Human chr5 + 64853509 64853509 64853509 AACATAAAATTTACCATCTTAACCATTATATTAGTCCATTCTTATGTTGCTATAAAGAAATATTT AACATAAAATTTACCATCTTAACCATTATATTTGTCCATTCTTATGTTGCTATAAAGAAATATTT A T CWC27 Ensembl:ENSG00000153015 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1231606431 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64618,RMVar_hsa_circ_71671 20769 RMVar_ID_20769 Human_SNP_ID_234967386 A-to-I Human chr5 - 65274727 65274727 65274727 TGAGCTGAGATTGTGCCACCGCACTCCAGCCTAGGTGACACAGTGAGACTCTGTCTCAGAAAACA TGAGCTGAGATTGTGCCACCGCACTCCAGCCTGGGTGACACAGTGAGACTCTGTCTCAGAAAACA T C ADAMTS6 Ensembl:ENSG00000049192 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934195156 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_910,RMVar_hsa_circ_111326,RMVar_hsa_circ_373079,RMVar_hsa_circ_374209,RMVar_hsa_circ_328090,RMVar_hsa_circ_125942,RMVar_hsa_circ_122319,RMVar_hsa_circ_231789,RMVar_hsa_circ_231791,RMVar_hsa_circ_231792,RMVar_hsa_circ_231790,RMVar_hsa_circ_231788,RMVar_hsa_circ_112972,RMVar_hsa_circ_45388,RMVar_hsa_circ_231793,RMVar_hsa_circ_231794,RMVar_hsa_circ_369761,RMVar_hsa_circ_51190,RMVar_hsa_circ_117098,RMVar_hsa_circ_12635,RMVar_hsa_circ_231797,RMVar_hsa_circ_2716,RMVar_hsa_circ_329309,RMVar_hsa_circ_231798,RMVar_hsa_circ_76430,RMVar_hsa_circ_118887,RMVar_hsa_circ_231801,RMVar_hsa_circ_231802,RMVar_hsa_circ_78474,RMVar_hsa_circ_335310,RMVar_hsa_circ_371899,RMVar_hsa_circ_231805,RMVar_hsa_circ_231806,RMVar_hsa_circ_231808,RMVar_hsa_circ_231807,RMVar_hsa_circ_323332,RMVar_hsa_circ_327086,RMVar_hsa_circ_321696,RMVar_hsa_circ_19528,RMVar_hsa_circ_285285,RMVar_hsa_circ_231811,RMVar_hsa_circ_325333,RMVar_hsa_circ_296677,RMVar_hsa_circ_101055,RMVar_hsa_circ_96491,RMVar_hsa_circ_125380,RMVar_hsa_circ_231813,RMVar_hsa_circ_231815,RMVar_hsa_circ_231816,RMVar_hsa_circ_231817,RMVar_hsa_circ_231814,RMVar_hsa_circ_316195,RMVar_hsa_circ_347876,RMVar_hsa_circ_269532,RMVar_hsa_circ_231819,RMVar_hsa_circ_111383,RMVar_hsa_circ_115178,RMVar_hsa_circ_231821,RMVar_hsa_circ_80132,RMVar_hsa_circ_231820,RMVar_hsa_circ_231818 20770 RMVar_ID_20770 Human_SNP_ID_235020832 A-to-I Human chr5 - 65503379 65503379 65503379 ATTATAGGCCGGACATAATGGCTCACGCCTGCAGAACAGCACTCTGGGAGGCCGAGGCAGGCGGA ATTATAGGCCGGACATAATGGCTCACGCCTGCGGAACAGCACTCTGGGAGGCCGAGGCAGGCGGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs977343841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15486725,Human_RBP_ID_25907850 20771 RMVar_ID_20771 Human_SNP_ID_235020936 A-to-I Human chr5 - 65503862 65503862 65503862 CACGAGGTCAGGAGTTCTAGACCAGTCTGACCAATATGGTGAAACCCCATCTCTACTAAAAAATA CACGAGGTCAGGAGTTCTAGACCAGTCTGACCGATATGGTGAAACCCCATCTCTACTAAAAAATA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1337278112 Functional Loss SNV dbSNP153 33..33 33 - - - 20772 RMVar_ID_20772 Human_SNP_ID_235021082 A-to-I Human chr5 - 65504395 65504395 65504395 TGGAGGGCAATGGCACGATCTTGGCCCACTGCAACCTCCCATCTCCCAGTTTCAAGCGATTCTCC TGGAGGGCAATGGCACGATCTTGGCCCACTGCCACCTCCCATCTCCCAGTTTCAAGCGATTCTCC T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1169036336 Functional Loss SNV dbSNP153 33..33 33 - - - 20773 RMVar_ID_20773 Human_SNP_ID_235021322 A-to-I Human chr5 - 65505137 65505137 65505137 AGGACAAAATAAATGTTGTAGCCTGGGCAGCAAAGTGAGACCCTGTCTCTACAAAAATAAAAATT AGGACAAAATAAATGTTGTAGCCTGGGCAGCAGAGTGAGACCCTGTCTCTACAAAAATAAAAATT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs905832953 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15570933 20774 RMVar_ID_20774 Human_SNP_ID_235021323 A-to-I Human chr5 - 65505137 65505137 65505137 AGGACAAAATAAATGTTGTAGCCTGGGCAGCAAAGTGAGACCCTGTCTCTACAAAAATAAAAATT AGGACAAAATAAATGTTGTAGCCTGGGCAGCACAGTGAGACCCTGTCTCTACAAAAATAAAAATT T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs905832953 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15570933 20775 RMVar_ID_20775 Human_SNP_ID_235021527 A-to-I Human chr5 - 65506166 65506166 65506166 TTGCCCAGGCTGGTCTTGAGCTCTTGGTCTCAAGACATTCTCCCGCCTGGGCCTCCCAAAGCACT TTGCCCAGGCTGGTCTTGAGCTCTTGGTCTCAGGACATTCTCCCGCCTGGGCCTCCCAAAGCACT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1211685062 Functional Loss SNV dbSNP153 33..33 33 - - - 20776 RMVar_ID_20776 Human_SNP_ID_235021550 A-to-I Human chr5 - 65506263 65506263 65506263 GCTTAAGCCATCTTCCTGTGCCACAAGTAGCTAGGACTACAGGTGCCTGCCACCATGCTAATTTT GCTTAAGCCATCTTCCTGTGCCACAAGTAGCTGGGACTACAGGTGCCTGCCACCATGCTAATTTT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1357905326 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15486775 20777 RMVar_ID_20777 Human_SNP_ID_235021640 A-to-I Human chr5 - 65506702 65506702 65506702 CAGCTCACTGCAATCTCCTCTTATCGGATTCAAGAGATTCTCCTGCCTTAGCCTCCTGAGCAGCT CAGCTCACTGCAATCTCCTCTTATCGGATTCAGGAGATTCTCCTGCCTTAGCCTCCTGAGCAGCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs574303788 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15486782 20778 RMVar_ID_20778 Human_SNP_ID_235025257 A-to-I Human chr5 - 65521627 65521627 65521627 CATTGCACTCCAGCCTGGGCGCCAAGAATGAAACTCTGTCTCAGAAATAAAAGTCTTATAAAAAC CATTGCACTCCAGCCTGGGCGCCAAGAATGAAGCTCTGTCTCAGAAATAAAAGTCTTATAAAAAC T C CENPK Ensembl:ENSG00000123219 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1378296426 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3774812 RMVar_hsa_circ_50255,RMVar_hsa_circ_336484,RMVar_hsa_circ_347019,RMVar_hsa_circ_378283,RMVar_hsa_circ_51783 20779 RMVar_ID_20779 Human_SNP_ID_235032881 A-to-I Human chr5 - 65551203 65551203 65551203 TCGTGTTGTCCAGGCTGGAGTACAGTGGCACAATCATGGCTCATTGCAGCCCCGATCTCCCGGGT TCGTGTTGTCCAGGCTGGAGTACAGTGGCACAGTCATGGCTCATTGCAGCCCCGATCTCCCGGGT T C CENPK Ensembl:ENSG00000123219 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1288894331 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_655797,Human_Splice_Rec_655812,Human_Splice_Rec_655813,Human_Splice_Rec_655882 RMVar_hsa_circ_50255,RMVar_hsa_circ_336484,RMVar_hsa_circ_51783,RMVar_hsa_circ_334931,RMVar_hsa_circ_282509,RMVar_hsa_circ_231838,RMVar_hsa_circ_51025,RMVar_hsa_circ_231837,RMVar_hsa_circ_86022,RMVar_hsa_circ_377649,RMVar_hsa_circ_231840,RMVar_hsa_circ_231841,RMVar_hsa_circ_311372,RMVar_hsa_circ_337385 20780 RMVar_ID_20780 Human_SNP_ID_235040823 A-to-I Human chr5 + 65581403 65581381 65581404 GAGCCCAGGACCAAGACCTGCCTGGGCAACATAGCAAGACCTCATCTCTACAAAAAATTTAAGAA GAGCCCAGGAC_______________________CAAGACCTCATCTCTACAAAAAATTTAAGAA CCAAGACCTGCCTGGGCAACATAG C PPWD1 Ensembl:ENSG00000113593 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1410798721 Functional Loss DEL dbSNP153 12..34 33 - - - RMVar_hsa_circ_314915,RMVar_hsa_circ_102951,RMVar_hsa_circ_119553,RMVar_hsa_circ_231846,RMVar_hsa_circ_231851,RMVar_hsa_circ_231847,RMVar_hsa_circ_308663,RMVar_hsa_circ_334525,RMVar_hsa_circ_114880,RMVar_hsa_circ_231852,RMVar_hsa_circ_231849,RMVar_hsa_circ_231850,RMVar_hsa_circ_231848,RMVar_hsa_circ_285236 20781 RMVar_ID_20781 Human_SNP_ID_235040839 A-to-I Human chr5 + 65581482 65581482 65581482 GTGGTGTGCACATGTGGTCTCAGCCATGCTGGAAGCTGATGTGGTAGGATCTCTTGAGCCAACGA GTGGTGTGCACATGTGGTCTCAGCCATGCTGGCAGCTGATGTGGTAGGATCTCTTGAGCCAACGA A C PPWD1 Ensembl:ENSG00000113593 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs558803674 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15489254 RMVar_hsa_circ_314915,RMVar_hsa_circ_102951,RMVar_hsa_circ_119553,RMVar_hsa_circ_231846,RMVar_hsa_circ_231851,RMVar_hsa_circ_231847,RMVar_hsa_circ_308663,RMVar_hsa_circ_334525,RMVar_hsa_circ_114880,RMVar_hsa_circ_231852,RMVar_hsa_circ_231849,RMVar_hsa_circ_231850,RMVar_hsa_circ_231848,RMVar_hsa_circ_285236 20782 RMVar_ID_20782 Human_SNP_ID_235054390 A-to-I Human chr5 + 65636307 65636307 65636307 CTGGGATTACAGGCGTGCGCACCGCTCTGGCTAATTTTTGTGTTTTTATTGGAGACCGTGTTTTG CTGGGATTACAGGCGTGCGCACCGCTCTGGCTGATTTTTGTGTTTTTATTGGAGACCGTGTTTTG A G TRAPPC13 Ensembl:ENSG00000113597 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1250763227 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20013,RMVar_hsa_circ_305413,RMVar_hsa_circ_315246,RMVar_hsa_circ_334679,RMVar_hsa_circ_299532,RMVar_hsa_circ_297363,RMVar_hsa_circ_231863,RMVar_hsa_circ_231864,RMVar_hsa_circ_231865 20783 RMVar_ID_20783 Human_SNP_ID_235055529 A-to-I Human chr5 + 65641123 65641123 65641123 CCCTGTCTAATTTTTTAATATTTTTTAGAGACAAGGTCTTGCTATGTTGCTCAAGCAGGTCTTGA CCCTGTCTAATTTTTTAATATTTTTTAGAGACGAGGTCTTGCTATGTTGCTCAAGCAGGTCTTGA A G TRAPPC13 Ensembl:ENSG00000113597 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1244365286 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20013,RMVar_hsa_circ_305413,RMVar_hsa_circ_334679,RMVar_hsa_circ_299532,RMVar_hsa_circ_297363,RMVar_hsa_circ_231864,RMVar_hsa_circ_231865 20784 RMVar_ID_20784 Human_SNP_ID_235062093 A-to-I Human chr5 - 65668796 65668796 65668796 TCAAGTGATTCTCGAGCCTTAAGCTCCCAAGTAGCTGGGATTACGGGCGCCCACCACCACGCCCA TCAAGTGATTCTCGAGCCTTAAGCTCCCAAGTGGCTGGGATTACGGGCGCCCACCACCACGCCCA T C SGTB Ensembl:ENSG00000197860 Protein coding 3'UTR GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;ASD brains,temporal_cortex;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,30559470,31158229,31158229 RNA-Seq:(High) rs1484609088 Functional Loss SNV dbSNP153 33..33 33 - - - 20785 RMVar_ID_20785 Human_SNP_ID_235062094 A-to-I Human chr5 - 65668799 65668799 65668799 GATTCAAGTGATTCTCGAGCCTTAAGCTCCCAAGTAGCTGGGATTACGGGCGCCCACCACCACGC GATTCAAGTGATTCTCGAGCCTTAAGCTCCCAGGTAGCTGGGATTACGGGCGCCCACCACCACGC T C SGTB Ensembl:ENSG00000197860 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1243410261 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7458854 20786 RMVar_ID_20786 Human_SNP_ID_235062105 A-to-I Human chr5 - 65668839 65668833 65668839 TGGTGTTGCAATGTCAGCTCACTGCAACCTCCACCTCCTGGATTCAAGTGATTCTCGAGCCTTAA TGGTGTTGCAATGTCAGCTCACTGCAACCTCC______TGGATTCAAGTGATTCTCGAGCCTTAA AGGAGGT A SGTB Ensembl:ENSG00000197860 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1289582799 Functional Loss DEL dbSNP153 33..38 33 - - - 20787 RMVar_ID_20787 Human_SNP_ID_235067019 A-to-I Human chr5 - 65691600 65691600 65691600 TCTTAGCCAGGCACAGTGGCTCACCGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCCAGTGGA TCTTAGCCAGGCACAGTGGCTCACCGCCTGTAGTCCCAGCACTTTGGGAGGCCGAGGCCAGTGGA T C SGTB Ensembl:ENSG00000197860 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs775942008 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51074,RMVar_hsa_circ_345223,RMVar_hsa_circ_24907,RMVar_hsa_circ_311101,RMVar_hsa_circ_231874,RMVar_hsa_circ_231872,RMVar_hsa_circ_231873,RMVar_hsa_circ_301608,RMVar_hsa_circ_345019,RMVar_hsa_circ_298141 20788 RMVar_ID_20788 Human_SNP_ID_235128650 A-to-I Human chr5 + 65946319 65946319 65946319 CCAGGAAGTCAAGGCTGCAGTGAGCTGAGATTACACCACTGCACTCCAGCCTGGGTGACAGAGCA CCAGGAAGTCAAGGCTGCAGTGAGCTGAGATTCCACCACTGCACTCCAGCCTGGGTGACAGAGCA A C ERBIN Ensembl:ENSG00000112851 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005807426 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87086,RMVar_hsa_circ_231909,RMVar_hsa_circ_231908 20789 RMVar_ID_20789 Human_SNP_ID_235166983 A-to-I Human chr5 + 66089869 66089869 66089869 GGCATGAGAATCGCTTGAACCTGGGAGGCAGTAAGCCAAAATTGTGCCTCTGAACTCCAGCCTGG GGCATGAGAATCGCTTGAACCTGGGAGGCAGTGAGCCAAAATTGTGCCTCTGAACTCCAGCCTGG A G AC025442.2 Ensembl:ENSG00000285999 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1245824087 Functional Loss SNV dbSNP153 33..33 33 - - - 20790 RMVar_ID_20790 Human_SNP_ID_235196876 A-to-I Human chr5 + 66213459 66213459 66213459 TGAACATCCTTGAAATGAATGGAAAGATAGGAAATGTCAGCAAAGGAACAGAAGATAGAAGAGCC TGAACATCCTTGAAATGAATGGAAAGATAGGAGATGTCAGCAAAGGAACAGAAGATAGAAGAGCC A G lnc-SREK1-4 RNACentral:URS00008B5A19 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs907597533 Functional Loss SNV dbSNP153 33..33 33 - - - 20791 RMVar_ID_20791 Human_SNP_ID_235196894 A-to-I Human chr5 + 66213521 66213521 66213521 GCCAATGGAAAATTTCAAACAAAAAATGCAGTAACTGTAATTTTAAATTTAAGCCCCTTCATTAA GCCAATGGAAAATTTCAAACAAAAAATGCAGTGACTGTAATTTTAAATTTAAGCCCCTTCATTAA A G lnc-SREK1-4 RNACentral:URS00008B5A19 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1436516237 Functional Loss SNV dbSNP153 33..33 33 - - - 20792 RMVar_ID_20792 Human_SNP_ID_235390338 A-to-I Human chr5 + 67018421 67018421 67018421 CCTGTGGTCCCAGCTACTCTGGAGACTGAGGCAGGAGGATTGCTTGAGCCCGAGAGGTCGCAGCT CCTGTGGTCCCAGCTACTCTGGAGACTGAGGCTGGAGGATTGCTTGAGCCCGAGAGGTCGCAGCT A T MAST4 Ensembl:ENSG00000069020 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs958869725 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39589 20793 RMVar_ID_20793 Human_SNP_ID_235902545 A-to-I Human chr5 + 69095461 69095461 69095461 CGACCTCGTGATCGGCCTGCCTCGGTCTTCCAAAGTGCCGGGATTACAGGCATGAGCCACCGCGC CGACCTCGTGATCGGCCTGCCTCGGTCTTCCACAGTGCCGGGATTACAGGCATGAGCCACCGCGC A C SLC30A5 Ensembl:ENSG00000145740 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335513456 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90454,RMVar_hsa_circ_231983 20794 RMVar_ID_20794 Human_SNP_ID_235902548 A-to-I Human chr5 + 69095474 69095474 69095474 GGCCTGCCTCGGTCTTCCAAAGTGCCGGGATTACAGGCATGAGCCACCGCGCCCGCCCAACATAA GGCCTGCCTCGGTCTTCCAAAGTGCCGGGATTGCAGGCATGAGCCACCGCGCCCGCCCAACATAA A G SLC30A5 Ensembl:ENSG00000145740 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1363256723 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90454,RMVar_hsa_circ_231983 20795 RMVar_ID_20795 Human_SNP_ID_235902756 A-to-I Human chr5 + 69096469 69096469 69096469 TTGTACTACTTACTTAGCAGAGTTGCCCTTCTATTGTAGTTTATTGCAGAATCAAATTCAACTCC TTGTACTACTTACTTAGCAGAGTTGCCCTTCTGTTGTAGTTTATTGCAGAATCAAATTCAACTCC A G SLC30A5 Ensembl:ENSG00000145740 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs117319810 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15500097 RMVar_hsa_circ_90454,RMVar_hsa_circ_231983 20796 RMVar_ID_20796 Human_SNP_ID_235902818 A-to-I Human chr5 + 69096837 69096837 69096837 ATAAAAATTAGCCAGGCACAGTGGCAGTGCCTATAGTTCCAGCTACTTGGGAGGCTAAGGCAGAA ATAAAAATTAGCCAGGCACAGTGGCAGTGCCTGTAGTTCCAGCTACTTGGGAGGCTAAGGCAGAA A G SLC30A5 Ensembl:ENSG00000145740 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs994544972 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90454,RMVar_hsa_circ_231983 20797 RMVar_ID_20797 Human_SNP_ID_235903026 A-to-I Human chr5 + 69097389 69097389 69097389 CGCCCGCCTGGGCCTCCCAAAGTGTTGGGATTACAGGCGTGAGCCACTGCGCCCTGCTCTTTCTT CGCCCGCCTGGGCCTCCCAAAGTGTTGGGATTGCAGGCGTGAGCCACTGCGCCCTGCTCTTTCTT A G SLC30A5 Ensembl:ENSG00000145740 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1055048063 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90454,RMVar_hsa_circ_231983 20798 RMVar_ID_20798 Human_SNP_ID_235903157 A-to-I Human chr5 + 69098050 69098050 69098050 AAAAACTTTTTGGAGAGACGGGGTCTCGCTGTATTGCCCAGGTTGGTCTTGAACTCCTGGACTCA AAAAACTTTTTGGAGAGACGGGGTCTCGCTGTCTTGCCCAGGTTGGTCTTGAACTCCTGGACTCA A C SLC30A5 Ensembl:ENSG00000145740 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1196486004 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90454,RMVar_hsa_circ_231983 20799 RMVar_ID_20799 Human_SNP_ID_235903211 A-to-I Human chr5 + 69098314 69098314 69098314 GGGAGGCCAAGGTGGGTGGATCACCTGAGGTCAGAAGTATGAGACCAGCCTGGCCAACCAGCATG GGGAGGCCAAGGTGGGTGGATCACCTGAGGTCGGAAGTATGAGACCAGCCTGGCCAACCAGCATG A G SLC30A5 Ensembl:ENSG00000145740 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1030527989 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17575273 RMVar_hsa_circ_90454,RMVar_hsa_circ_231983 20800 RMVar_ID_20800 Human_SNP_ID_235903389 A-to-I Human chr5 + 69099280 69099280 69099280 ATTCTTTACCTGGACTCCGTAATTGTTAATGTATCGTCCTGTGTAATTTATTATTCTCTCTGAAT ATTCTTTACCTGGACTCCGTAATTGTTAATGTGTCGTCCTGTGTAATTTATTATTCTCTCTGAAT A G SLC30A5 Ensembl:ENSG00000145740 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1265812991 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90454,RMVar_hsa_circ_231983 20801 RMVar_ID_20801 Human_SNP_ID_235903430 A-to-I Human chr5 + 69099433 69099432 69099434 TAAAAACATGGACATTCTCTTATAAAGCCAGCAGAGTTGTCTACTTCAGGAAATTTAAGTGACCT TAAAAACATGGACATTCTCTTATAAAGCCAGC__AGTTGTCTACTTCAGGAAATTTAAGTGACCT CAG C SLC30A5 Ensembl:ENSG00000145740 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1294430337 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_90454,RMVar_hsa_circ_231983 20802 RMVar_ID_20802 Human_SNP_ID_235903546 A-to-I Human chr5 + 69099992 69099991 69099993 AAATGTTGTGGTTGGTTGGTTCGTTTTGAGACAGAGTCTCGCTCTGTTACCTAGGCTGAAGTGCA AAATGTTGTGGTTGGTTGGTTCGTTTTGAGAC__AGTCTCGCTCTGTTACCTAGGCTGAAGTGCA CAG C SLC30A5 Ensembl:ENSG00000145740 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs369138142 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_15500137 RMVar_hsa_circ_90454,RMVar_hsa_circ_231983 20803 RMVar_ID_20803 Human_SNP_ID_235903668 A-to-I Human chr5 + 69100509 69100509 69100509 CAAAATGTTAACAGTAGGGCGCGGTGGCTCACACCTGTAATCCTAGCACTTTGGGAGACCAAGGC CAAAATGTTAACAGTAGGGCGCGGTGGCTCACCCCTGTAATCCTAGCACTTTGGGAGACCAAGGC A C SLC30A5 Ensembl:ENSG00000145740 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs372963215 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90454,RMVar_hsa_circ_231983 20804 RMVar_ID_20804 Human_SNP_ID_235907191 A-to-I Human chr5 + 69116103 69116103 69116103 TTATTAGTGCTCTCCTTTTTGGAAATTTTTGGACACATCCAATAACAGACCAGCTTCGGGCTATG TTATTAGTGCTCTCCTTTTTGGAAATTTTTGGGCACATCCAATAACAGACCAGCTTCGGGCTATG A G SLC30A5 Ensembl:ENSG00000145740 Protein coding 5'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1460716057 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1322531,Human_RBP_ID_15500250,Human_RBP_ID_17530903,Human_RBP_ID_18051644,Human_RBP_ID_27337846,Human_RBP_ID_27516973 RMVar_hsa_circ_2097,RMVar_hsa_circ_294195,RMVar_hsa_circ_311968,RMVar_hsa_circ_318639,RMVar_hsa_circ_294520,RMVar_hsa_circ_231988,RMVar_hsa_circ_231990,RMVar_hsa_circ_231989,RMVar_hsa_circ_231987,RMVar_hsa_circ_231991,RMVar_hsa_circ_58716,RMVar_hsa_circ_370187,RMVar_hsa_circ_231995,RMVar_hsa_circ_296358,RMVar_hsa_circ_304957,RMVar_hsa_circ_316503,RMVar_hsa_circ_298166,RMVar_hsa_circ_231993,RMVar_hsa_circ_231994,RMVar_hsa_circ_231992,RMVar_hsa_circ_232003,RMVar_hsa_circ_4185,RMVar_hsa_circ_344909,RMVar_hsa_circ_307935,RMVar_hsa_circ_273371,RMVar_hsa_circ_231999,RMVar_hsa_circ_268985,RMVar_hsa_circ_232001,RMVar_hsa_circ_113887,RMVar_hsa_circ_279605,RMVar_hsa_circ_338920,RMVar_hsa_circ_271095,RMVar_hsa_circ_232005,RMVar_hsa_circ_59732,RMVar_hsa_circ_232004,RMVar_hsa_circ_232002 20805 RMVar_ID_20805 Human_SNP_ID_235908340 A-to-I Human chr5 + 69120328 69120328 69120328 ATTGCTTGAACCTGGGAGGCAGAGGTTGCAATAAGCCGAGATCATGCCACTGCACTCCAGCCTGG ATTGCTTGAACCTGGGAGGCAGAGGTTGCAATGAGCCGAGATCATGCCACTGCACTCCAGCCTGG A G SLC30A5 Ensembl:ENSG00000145740 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs887483922 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_294195,RMVar_hsa_circ_294520,RMVar_hsa_circ_231990,RMVar_hsa_circ_231989,RMVar_hsa_circ_231991,RMVar_hsa_circ_58716,RMVar_hsa_circ_370187,RMVar_hsa_circ_316503,RMVar_hsa_circ_298166,RMVar_hsa_circ_231993,RMVar_hsa_circ_231992,RMVar_hsa_circ_232003,RMVar_hsa_circ_4185,RMVar_hsa_circ_344909,RMVar_hsa_circ_307935,RMVar_hsa_circ_268985,RMVar_hsa_circ_232001,RMVar_hsa_circ_113887,RMVar_hsa_circ_338920,RMVar_hsa_circ_271095,RMVar_hsa_circ_232005,RMVar_hsa_circ_232004,RMVar_hsa_circ_17797,RMVar_hsa_circ_116381,RMVar_hsa_circ_232006,RMVar_hsa_circ_277582,RMVar_hsa_circ_232007 20806 RMVar_ID_20806 Human_SNP_ID_235909149 A-to-I Human chr5 + 69124045 69124045 69124045 TGAGGCAGGAGAATGGCGTGAACCCGGGAGGCAGAGCTTGCAGTGAGCCGAGACCACGCCACTAC TGAGGCAGGAGAATGGCGTGAACCCGGGAGGCGGAGCTTGCAGTGAGCCGAGACCACGCCACTAC A G SLC30A5 Ensembl:ENSG00000145740 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs555339790 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_165312 RMVar_hsa_circ_58716,RMVar_hsa_circ_344909,RMVar_hsa_circ_268985,RMVar_hsa_circ_271095,RMVar_hsa_circ_232005,RMVar_hsa_circ_232004,RMVar_hsa_circ_277582,RMVar_hsa_circ_232008,RMVar_hsa_circ_232007,RMVar_hsa_circ_321791,RMVar_hsa_circ_232010,RMVar_hsa_circ_232009,RMVar_hsa_circ_350901,RMVar_hsa_circ_306551 20807 RMVar_ID_20807 Human_SNP_ID_235922250 A-to-I Human chr5 + 69174936 69174936 69174936 CAGCTGGTTGGTGTCACTGCCATGTTTATTGCAAGCAAATATGAAGAAATGTACCCTCCAGAAAT CAGCTGGTTGGTGTCACTGCCATGTTTATTGCGAGCAAATATGAAGAAATGTACCCTCCAGAAAT A G CCNB1 Ensembl:ENSG00000134057 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs372950417 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1657119,Human_RBP_ID_1998570,Human_RBP_ID_8620952,Human_RBP_ID_9397862,Human_RBP_ID_18846085,Human_RBP_ID_19014887,Human_RBP_ID_22099435,Human_RBP_ID_24113999,Human_RBP_ID_27516990 Human_Splice_Rec_658004,Human_Splice_Rec_658018,Human_Splice_Rec_658032,Human_Splice_Rec_658042,Human_Splice_Rec_658056 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 20808 RMVar_ID_20808 Human_SNP_ID_235925461 A-to-I Human chr5 - 69186053 69186052 69186053 CAGTAATCCCAGCACTTTGGGAGGCTGAGGCAAGAGGATCTGTGGAGCCCAGGAGTTCGAGACCA CAGTAATCCCAGCACTTTGGGAGGCTGAGGCA_GAGGATCTGTGGAGCCCAGGAGTTCGAGACCA CT C lnc-CCDC125-1,lnc-CCDC125-1:2,lnc-CCDC125-1:3,lnc-CCDC125-1:4,lnc-CCDC125-1:5 RNACentral:URS0000D5ABD5,RNACentral:URS0000D5DFD5,RNACentral:URS00008BC80B,RNACentral:URS00008C2956,RNACentral:URS0000D57E3D lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,intron,intron,exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs918335447 Functional Loss DEL dbSNP153 33..33 33 - - - 20809 RMVar_ID_20809 Human_SNP_ID_235925684 A-to-I Human chr5 - 69186972 69186972 69186972 AAAATTAATCAGGCACAGGGGCACACGCTTGTAATCCCAGCTACTCGGGAGGCTGAGACAGGAAA AAAATTAATCAGGCACAGGGGCACACGCTTGTTATCCCAGCTACTCGGGAGGCTGAGACAGGAAA T A AC022107.1 Ensembl:ENSG00000280187 Other exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs925074573 Functional Loss SNV dbSNP153 33..33 33 - - - 20810 RMVar_ID_20810 Human_SNP_ID_235928862 A-to-I Human chr5 + 69198473 69198473 69198473 TACAACTCCCAGGTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACTATGTTGGCCAGGCTGG TACAACTCCCAGGTAATTTTTGTATTTTTAGTGGAGACGGGGTTTCACTATGTTGGCCAGGCTGG A G CENPH Ensembl:ENSG00000153044 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1461177712 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119958,RMVar_hsa_circ_103108,RMVar_hsa_circ_232023,RMVar_hsa_circ_353095,RMVar_hsa_circ_64048,RMVar_hsa_circ_232024,RMVar_hsa_circ_73625,RMVar_hsa_circ_320423 20811 RMVar_ID_20811 Human_SNP_ID_235930929 A-to-I Human chr5 + 69205920 69205920 69205920 TTTAGTAGAGACCGGATTTCACCATATTAGCTAGGATGGTCTCCATCTCCTGACCTCGTGATCCG TTTAGTAGAGACCGGATTTCACCATATTAGCTGGGATGGTCTCCATCTCCTGACCTCGTGATCCG A G CENPH Ensembl:ENSG00000153044 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1162298598 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119958,RMVar_hsa_circ_103108,RMVar_hsa_circ_232023,RMVar_hsa_circ_353095,RMVar_hsa_circ_232024,RMVar_hsa_circ_73625,RMVar_hsa_circ_320423,RMVar_hsa_circ_84334,RMVar_hsa_circ_112431,RMVar_hsa_circ_232025,RMVar_hsa_circ_232026 20812 RMVar_ID_20812 Human_SNP_ID_235931414 A-to-I Human chr5 + 69207776 69207776 69207776 GAGGCTGCAGTGAGCCGAGATTGTACCACTGCACTCCAGCCTAGGCAACAGTGAGACTCCATCTC GAGGCTGCAGTGAGCCGAGATTGTACCACTGCGCTCCAGCCTAGGCAACAGTGAGACTCCATCTC A G CENPH Ensembl:ENSG00000153044 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs937593213 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119958,RMVar_hsa_circ_103108,RMVar_hsa_circ_232023,RMVar_hsa_circ_353095,RMVar_hsa_circ_232024,RMVar_hsa_circ_73625,RMVar_hsa_circ_320423,RMVar_hsa_circ_84334,RMVar_hsa_circ_112431,RMVar_hsa_circ_232025,RMVar_hsa_circ_232026 20813 RMVar_ID_20813 Human_SNP_ID_235932051 A-to-I Human chr5 + 69210267 69210267 69210267 GGCAGTCCACCGCCTCGGCCTACCGAAGTGCTAGGATTACAGACGTAAGCCACCGAGCCTGGTCT GGCAGTCCACCGCCTCGGCCTACCGAAGTGCTGGGATTACAGACGTAAGCCACCGAGCCTGGTCT A G CENPH Ensembl:ENSG00000153044 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1217375901 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_645310,Human_RBP_ID_26826314 RMVar_hsa_circ_119958,RMVar_hsa_circ_103108,RMVar_hsa_circ_232023,RMVar_hsa_circ_232024,RMVar_hsa_circ_84334,RMVar_hsa_circ_112431,RMVar_hsa_circ_232025,RMVar_hsa_circ_232026 20814 RMVar_ID_20814 Human_SNP_ID_235932118 A-to-I Human chr5 + 69210556 69210555 69210557 GTATTTTCAACATTTTTTTTTCCCCTTGAGATAGAGGCTCGCTCTGTTACCCAGGCTGGCATGCA GTATTTTCAACATTTTTTTTTCCCCTTGAGAT__AGGCTCGCTCTGTTACCCAGGCTGGCATGCA TAG T RF00017-4528 RNACentral:URS00009A4D01 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1208304089 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_645313,Human_RBP_ID_15501063 20815 RMVar_ID_20815 Human_SNP_ID_235933052 A-to-I Human chr5 + 69214170 69214170 69214170 GTGCAGTGGTACGATCTTGGCTCACTGTGAACAACTTCCGCCTCCCAGGTTCAAGCAATTCTCAT GTGCAGTGGTACGATCTTGGCTCACTGTGAACGACTTCCGCCTCCCAGGTTCAAGCAATTCTCAT A G RF00017-4528 RNACentral:URS00009A4D01 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs966795833 Functional Loss SNV dbSNP153 33..33 33 - - - 20816 RMVar_ID_20816 Human_SNP_ID_235933053 A-to-I Human chr5 + 69214184 69214184 69214184 TCTTGGCTCACTGTGAACAACTTCCGCCTCCCAGGTTCAAGCAATTCTCATGCCTCGGCTTCCAA TCTTGGCTCACTGTGAACAACTTCCGCCTCCCGGGTTCAAGCAATTCTCATGCCTCGGCTTCCAA A G RF00017-4528 RNACentral:URS00009A4D01 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1195291718 Functional Loss SNV dbSNP153 33..33 33 - - - 20817 RMVar_ID_20817 Human_SNP_ID_235933054 A-to-I Human chr5 + 69214190 69214190 69214190 CTCACTGTGAACAACTTCCGCCTCCCAGGTTCAAGCAATTCTCATGCCTCGGCTTCCAAGTAGCT CTCACTGTGAACAACTTCCGCCTCCCAGGTTCGAGCAATTCTCATGCCTCGGCTTCCAAGTAGCT A G RF00017-4528 RNACentral:URS00009A4D01 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978133554 Functional Loss SNV dbSNP153 33..33 33 - - - 20818 RMVar_ID_20818 Human_SNP_ID_235935478 A-to-I Human chr5 + 69223353 69223353 69223353 CACCCACCTCGGCCTCTCAAAGTGCTGGCATTACAGGTGTGAGCCACCATGCCCGGCCGAGAAGT CACCCACCTCGGCCTCTCAAAGTGCTGGCATTGCAGGTGTGAGCCACCATGCCCGGCCGAGAAGT A G MRPS36 Ensembl:ENSG00000134056 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1245126415 Functional Loss SNV dbSNP153 33..33 33 - - - 20819 RMVar_ID_20819 Human_SNP_ID_235935915 A-to-I Human chr5 + 69225204 69225204 69225204 TGAGCTCACTGCAACCTCTGCCTCCTTGGTTCAAGTGATCCTCCCACCTCAGCCTCCCAAGTAGC TGAGCTCACTGCAACCTCTGCCTCCTTGGTTCGAGTGATCCTCCCACCTCAGCCTCCCAAGTAGC A G MRPS36 Ensembl:ENSG00000134056 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1425973631 Functional Loss SNV dbSNP153 33..33 33 - - - 20820 RMVar_ID_20820 Human_SNP_ID_235942724 A-to-I Human chr5 + 69252613 69252613 69252613 CTCACTGCAGCCTCAAACTTAGGTACTCAAGCAGTTCTCCCACCTCAGCCTCTTGAGTAGCTAGG CTCACTGCAGCCTCAAACTTAGGTACTCAAGCTGTTCTCCCACCTCAGCCTCTTGAGTAGCTAGG A T CDK7 Ensembl:ENSG00000134058 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs997921007 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112536,RMVar_hsa_circ_344953,RMVar_hsa_circ_377542,RMVar_hsa_circ_333009,RMVar_hsa_circ_232028,RMVar_hsa_circ_232029 20821 RMVar_ID_20821 Human_SNP_ID_235942756 A-to-I Human chr5 + 69252743 69252743 69252743 GTTGCTCAGGCTTCTCTCAAACTCCTGGCCTCAAGCTATCCTCCCACCTCGGCCTCCCAAAGTGC GTTGCTCAGGCTTCTCTCAAACTCCTGGCCTCGAGCTATCCTCCCACCTCGGCCTCCCAAAGTGC A G CDK7 Ensembl:ENSG00000134058 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs916642923 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112536,RMVar_hsa_circ_344953,RMVar_hsa_circ_377542,RMVar_hsa_circ_333009,RMVar_hsa_circ_232028,RMVar_hsa_circ_232029 20822 RMVar_ID_20822 Human_SNP_ID_235946810 A-to-I Human chr5 + 69269205 69269205 69269205 CACCTTGAAAAGTCTCCCTCTTACTTTCTTTCAGGTTCCTTTTTTGCCAGGAGATTCAGACCTTG CACCTTGAAAAGTCTCCCTCTTACTTTCTTTCCGGTTCCTTTTTTGCCAGGAGATTCAGACCTTG A C CDK7 Ensembl:ENSG00000134058 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1166547406 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5151277,Human_RBP_ID_25932540,Human_RBP_ID_26826317 Human_Splice_Rec_658167,Human_Splice_Rec_658189,Human_Splice_Rec_658233,Human_Splice_Rec_658273,Human_Splice_Rec_658289,Human_Splice_Rec_658319,Human_Splice_Rec_658337,Human_Splice_Rec_658355 RMVar_hsa_circ_2933,RMVar_hsa_circ_344953,RMVar_hsa_circ_377542,RMVar_hsa_circ_269395,RMVar_hsa_circ_117259,RMVar_hsa_circ_232033,RMVar_hsa_circ_15555,RMVar_hsa_circ_372197,RMVar_hsa_circ_335788,RMVar_hsa_circ_232035,RMVar_hsa_circ_232034,RMVar_hsa_circ_373010,RMVar_hsa_circ_268378 20823 RMVar_ID_20823 Human_SNP_ID_235949815 A-to-I Human chr5 - 69280917 69280917 69280917 ATGCACCTGTTGTCCCAGCTACTCAGGGGCTGAGGCAGGAGGATGGCATGAGCCCAGGAGCTTGA ATGCACCTGTTGTCCCAGCTACTCAGGGGCTGGGGCAGGAGGATGGCATGAGCCCAGGAGCTTGA T C CCDC125 Ensembl:ENSG00000183323 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1134773 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24114119 20824 RMVar_ID_20824 Human_SNP_ID_235949817 A-to-I Human chr5 - 69280925 69280925 69280925 ATGGTGGCATGCACCTGTTGTCCCAGCTACTCAGGGGCTGAGGCAGGAGGATGGCATGAGCCCAG ATGGTGGCATGCACCTGTTGTCCCAGCTACTCGGGGGCTGAGGCAGGAGGATGGCATGAGCCCAG T C CCDC125 Ensembl:ENSG00000183323 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1175969661 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24114119 20825 RMVar_ID_20825 Human_SNP_ID_235949897 A-to-I Human chr5 - 69281278 69281278 69281278 TTGCTCAGGCTGGTGCCAAACTCCTGGCCTCAAGGGATCCTCCTGCCTCAGCCTCTCAAAGTGCT TTGCTCAGGCTGGTGCCAAACTCCTGGCCTCAGGGGATCCTCCTGCCTCAGCCTCTCAAAGTGCT T C CCDC125 Ensembl:ENSG00000183323 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs918267178 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_645351,Human_RBP_ID_26529710 20826 RMVar_ID_20826 Human_SNP_ID_235950101 A-to-I Human chr5 - 69281964 69281964 69281964 ATCGCTTGAACCTGGGAGGCGGGGGTTGTGGTAAGCCGAGACTGTGTCATTGCACTCCAGCCTGG ATCGCTTGAACCTGGGAGGCGGGGGTTGTGGTGAGCCGAGACTGTGTCATTGCACTCCAGCCTGG T C CCDC125 Ensembl:ENSG00000183323 Protein coding 3'UTR GSE100210;GSE112787;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;293 Flip-In T-REx cells,empty vector;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,29967493,31158229,31158229,31158229 RNA-Seq:(High) rs1169916123 Functional Loss SNV dbSNP153 33..33 33 - - - 20827 RMVar_ID_20827 Human_SNP_ID_235950125 A-to-I Human chr5 - 69282080 69282080 69282080 CAAGACCAGTCTGACCAACATGGAGAAACCCCATCTCTACTAAAAATACAAAAAATTAGCTAGGC CAAGACCAGTCTGACCAACATGGAGAAACCCCGTCTCTACTAAAAATACAAAAAATTAGCTAGGC T C CCDC125 Ensembl:ENSG00000183323 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1005699404 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_166141 20828 RMVar_ID_20828 Human_SNP_ID_235950178 A-to-I Human chr5 - 69282399 69282399 69282399 TGCCACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTTACCATGTTAGCCAGGC TGCCACCACGCCCAGCTAATTTTTGTATTTTTGGTAGAGACGGGGTTTTACCATGTTAGCCAGGC T C CCDC125 Ensembl:ENSG00000183323 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs948742314 Functional Loss SNV dbSNP153 33..33 33 - - - 20829 RMVar_ID_20829 Human_SNP_ID_235950182 A-to-I Human chr5 - 69282414 69282414 69282414 CGGATTACAGGCATGTGCCACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTTA CGGATTACAGGCATGTGCCACCACGCCCAGCTGATTTTTGTATTTTTAGTAGAGACGGGGTTTTA T C CCDC125 Ensembl:ENSG00000183323 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1436248696 Functional Loss SNV dbSNP153 33..33 33 - - - 20830 RMVar_ID_20830 Human_SNP_ID_235950192 A-to-I Human chr5 - 69282440 69282440 69282440 CTCCTGCCTCAGCCTCCCGAGTAACTCGGATTACAGGCATGTGCCACCACGCCCAGCTAATTTTT CTCCTGCCTCAGCCTCCCGAGTAACTCGGATTGCAGGCATGTGCCACCACGCCCAGCTAATTTTT T C CCDC125 Ensembl:ENSG00000183323 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1407225318 Functional Loss SNV dbSNP153 33..33 33 - - - 20831 RMVar_ID_20831 Human_SNP_ID_235950206 A-to-I Human chr5 - 69282475 69282475 69282475 TTCACTGCAACCTCCGCCTCCCGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAACTCGGA TTCACTGCAACCTCCGCCTCCCGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCCGAGTAACTCGGA T C CCDC125 Ensembl:ENSG00000183323 Protein coding 3'UTR GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs958573824 Functional Loss SNV dbSNP153 33..33 33 - - - 20832 RMVar_ID_20832 Human_SNP_ID_235958156 A-to-I Human chr5 + 69313864 69313863 69313864 ACCTTGATGACACCATCAGAGACAGCCACAACAGAGGCCATGTTTCCAGAAGCAAAAAGGAGAGG ACCTTGATGACACCATCAGAGACAGCCACAAC_GAGGCCATGTTTCCAGAAGCAAAAAGGAGAGG CA C RF00017-4528 RNACentral:URS00009A4D01 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559732365 Functional Loss DEL dbSNP153 33..33 33 - - - 20833 RMVar_ID_20833 Human_SNP_ID_235958158 A-to-I Human chr5 + 69313864 69313864 69313864 ACCTTGATGACACCATCAGAGACAGCCACAACAGAGGCCATGTTTCCAGAAGCAAAAAGGAGAGG ACCTTGATGACACCATCAGAGACAGCCACAACGGAGGCCATGTTTCCAGAAGCAAAAAGGAGAGG A G RF00017-4528 RNACentral:URS00009A4D01 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350970569 Functional Loss SNV dbSNP153 33..33 33 - - - 20834 RMVar_ID_20834 Human_SNP_ID_235958160 A-to-I Human chr5 + 69313879 69313879 69313879 TCAGAGACAGCCACAACAGAGGCCATGTTTCCAGAAGCAAAAAGGAGAGGGCATGGAGAGCTGCA TCAGAGACAGCCACAACAGAGGCCATGTTTCCGGAAGCAAAAAGGAGAGGGCATGGAGAGCTGCA A G RF00017-4528 RNACentral:URS00009A4D01 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1308096731 Functional Loss SNV dbSNP153 33..33 33 - - - 20835 RMVar_ID_20835 Human_SNP_ID_235958947 A-to-I Human chr5 - 69316788 69316788 69316788 CCCAAACAGGCTACGTCTGGTAGCTGATGCCTATAATCCCAGCATTTTGGGAGGCCGAGGTGGGA CCCAAACAGGCTACGTCTGGTAGCTGATGCCTGTAATCCCAGCATTTTGGGAGGCCGAGGTGGGA T C CCDC125 Ensembl:ENSG00000183323 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1425880119 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_232047,RMVar_hsa_circ_232050 20836 RMVar_ID_20836 Human_SNP_ID_235968146 A-to-I Human chr5 - 69354964 69354964 69354964 AATTAGCCGGGCATGGTGGCAGGCACCTGTACAGTCCCAGCTACTCTGGAGGCTGAGGCAGGAGA AATTAGCCGGGCATGGTGGCAGGCACCTGTACGGTCCCAGCTACTCTGGAGGCTGAGGCAGGAGA T C AK6 Ensembl:ENSG00000085231 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1438063040 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_164601 RMVar_hsa_circ_232051,RMVar_hsa_circ_78534 20837 RMVar_ID_20837 Human_SNP_ID_235968247 A-to-I Human chr5 - 69355418 69355418 69355418 CAAGCAATTCTTGTGCCTCAGCCTCCTGACTAACAGACCACGGGCACATGCCACCTTGCCTGGCT CAAGCAATTCTTGTGCCTCAGCCTCCTGACTAGCAGACCACGGGCACATGCCACCTTGCCTGGCT T C AK6 Ensembl:ENSG00000085231 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1358156633 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_232051,RMVar_hsa_circ_78534 20838 RMVar_ID_20838 Human_SNP_ID_235969135 A-to-I Human chr5 - 69358996 69358996 69358996 GCTCAAGAGATCCTCCCACCTCGGCCTCTGAAAGTGCTAGGATTATAAGCGCGAACCACCATGCT GCTCAAGAGATCCTCCCACCTCGGCCTCTGAATGTGCTAGGATTATAAGCGCGAACCACCATGCT T A AK6 Ensembl:ENSG00000085231 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1176798156 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_323024 20839 RMVar_ID_20839 Human_SNP_ID_235969164 A-to-I Human chr5 - 69359124 69359124 69359124 CTCCCACCTCAACCTCCAGAGTAGCTGGGACTATAGGCTGGCACCGCCATGCTGGGCTAATTTTT CTCCCACCTCAACCTCCAGAGTAGCTGGGACTGTAGGCTGGCACCGCCATGCTGGGCTAATTTTT T C AK6 Ensembl:ENSG00000085231 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1016175050 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_323024 20840 RMVar_ID_20840 Human_SNP_ID_235969183 A-to-I Human chr5 - 69359223 69359223 69359223 TAAAAAAAAAAAATTTTTTTTTTTTTGAGACAAGGTATCACTGTCACCCTAACTGGAATACAGTG TAAAAAAAAAAAATTTTTTTTTTTTTGAGACAGGGTATCACTGTCACCCTAACTGGAATACAGTG T C AK6 Ensembl:ENSG00000085231 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1257569678 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_323024 20841 RMVar_ID_20841 Human_SNP_ID_235970009 A-to-I Human chr5 - 69362299 69362299 69362299 TGCCCTTTGGGGGTATAGCAATGTGTGAAGACATTTTGGGTTGTCACATGGAGGGGGAGGTGATG TGCCCTTTGGGGGTATAGCAATGTGTGAAGACTTTTTGGGTTGTCACATGGAGGGGGAGGTGATG T A AK6 Ensembl:ENSG00000085231 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs28438532 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_323024 20842 RMVar_ID_20842 Human_SNP_ID_235970010 A-to-I Human chr5 - 69362299 69362299 69362299 TGCCCTTTGGGGGTATAGCAATGTGTGAAGACATTTTGGGTTGTCACATGGAGGGGGAGGTGATG TGCCCTTTGGGGGTATAGCAATGTGTGAAGACGTTTTGGGTTGTCACATGGAGGGGGAGGTGATG T C AK6 Ensembl:ENSG00000085231 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs28438532 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_323024 20843 RMVar_ID_20843 Human_SNP_ID_235970192 A-to-I Human chr5 - 69363106 69363106 69363106 ATCCTGCCTCAGCCTCCCTTGTAGCTGGGACTACAGGCACACACCATCCTGCCGGGCTAACTTAA ATCCTGCCTCAGCCTCCCTTGTAGCTGGGACTGCAGGCACACACCATCCTGCCGGGCTAACTTAA T C AK6 Ensembl:ENSG00000085231 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560565263 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_323024 20844 RMVar_ID_20844 Human_SNP_ID_235971617 A-to-I Human chr5 - 69367947 69367947 69367947 TTGGCCAGGCTGGTCTCGAACTCCTGCGCTTAAGCGATCCTCCCGCCTTCTCCTCCCAAATTGCT TTGGCCAGGCTGGTCTCGAACTCCTGCGCTTAGGCGATCCTCCCGCCTTCTCCTCCCAAATTGCT T C AK6,TAF9 Ensembl:ENSG00000085231,Ensembl:ENSG00000273841 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027137905 Functional Loss SNV dbSNP153 33..33 33 - - - 20845 RMVar_ID_20845 Human_SNP_ID_236007178 A-to-I Human chr5 + 69503979 69503979 69503979 GGAATTAGCCAGGCATGGTGGTGCAGGTCTGTAGTCCTAGCTACTTGGGAGGCTGAGGTAGGAGG GGAATTAGCCAGGCATGGTGGTGCAGGTCTGTGGTCCTAGCTACTTGGGAGGCTGAGGTAGGAGG A G OCLN Ensembl:ENSG00000197822 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs897484008 Functional Loss SNV dbSNP153 33..33 33 - - - 20846 RMVar_ID_20846 Human_SNP_ID_236049513 A-to-I Human chr5 + 70049282 70049282 70049282 CCTAAGCAACATGCCGAAACCCCGTCTCTACTAAATACAAAAAATAGCTGAGCTTGGTGGCGCAC CCTAAGCAACATGCCGAAACCCCGTCTCTACTGAATACAAAAAATAGCTGAGCTTGGTGGCGCAC A G RF00017-462,lnc-NAIP-5-001,lnc-NAIP-5-001:2 RNACentral:URS00009A2CEE,RNACentral:URS00008C1E81,RNACentral:URS00008C1F17 SRP RNA,lincRNA,lincRNA intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs963414068 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108571,RMVar_hsa_circ_232074,RMVar_hsa_circ_90222,RMVar_hsa_circ_232077,RMVar_hsa_circ_118125,RMVar_hsa_circ_232081,RMVar_hsa_circ_115657,RMVar_hsa_circ_232080,RMVar_hsa_circ_89196,RMVar_hsa_circ_101850,RMVar_hsa_circ_86263,RMVar_hsa_circ_232084,RMVar_hsa_circ_232085,RMVar_hsa_circ_121875,RMVar_hsa_circ_85967,RMVar_hsa_circ_232086,RMVar_hsa_circ_232087,RMVar_hsa_circ_232088,RMVar_hsa_circ_115485,RMVar_hsa_circ_99671,RMVar_hsa_circ_83229,RMVar_hsa_circ_232103,RMVar_hsa_circ_232104,RMVar_hsa_circ_232105 20847 RMVar_ID_20847 Human_SNP_ID_236051844 A-to-I Human chr5 + 70080294 70080294 70080294 CGGAGGTTGCAGTGAGCCAAGATCGTGCCACTACACTCCAGCCTGGGTGACTCAGTGACTGTCTC CGGAGGTTGCAGTGAGCCAAGATCGTGCCACTGCACTCCAGCCTGGGTGACTCAGTGACTGTCTC A G RF00017-462,lnc-NAIP-5-001,lnc-NAIP-5-001:2,5N5C_A-001 RNACentral:URS00009A2CEE,RNACentral:URS00008C1E81,RNACentral:URS00008C1F17,RNACentral:URS0000E3DF5E SRP RNA,lincRNA,lincRNA,Other intron,intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1171954252 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108571,RMVar_hsa_circ_232074,RMVar_hsa_circ_90222,RMVar_hsa_circ_232077,RMVar_hsa_circ_118125,RMVar_hsa_circ_232081,RMVar_hsa_circ_115657,RMVar_hsa_circ_232080,RMVar_hsa_circ_89196,RMVar_hsa_circ_101850,RMVar_hsa_circ_86263,RMVar_hsa_circ_232084,RMVar_hsa_circ_232085,RMVar_hsa_circ_121875,RMVar_hsa_circ_85967,RMVar_hsa_circ_232086,RMVar_hsa_circ_232087,RMVar_hsa_circ_232088,RMVar_hsa_circ_115485,RMVar_hsa_circ_99671,RMVar_hsa_circ_83229,RMVar_hsa_circ_232103,RMVar_hsa_circ_232104,RMVar_hsa_circ_232105,RMVar_hsa_circ_83174,RMVar_hsa_circ_87382,RMVar_hsa_circ_232110,RMVar_hsa_circ_232111 20848 RMVar_ID_20848 Human_SNP_ID_236056301 A-to-I Human chr5 - 70122683 70122683 70122683 CCAGCTAATTTTTTTTTCTTTTTTTAAGAGACAGGGTCTCTCTATGTTGCCCAGGCTGCTCTCAG CCAGCTAATTTTTTTTTCTTTTTTTAAGAGACTGGGTCTCTCTATGTTGCCCAGGCTGCTCTCAG T A NAIPP2 Ensembl:ENSG00000179978 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432436642 Functional Loss SNV dbSNP153 33..33 33 - - - 20849 RMVar_ID_20849 Human_SNP_ID_236073421 A-to-I Human chr5 + 70439297 70439297 70439297 GTAGAATTAATAGACAAAGGGTTGGGTGCGGTAGCTCCTGCCTGTAATGCTAGCACTTTGGGAGG GTAGAATTAATAGACAAAGGGTTGGGTGCGGTGGCTCCTGCCTGTAATGCTAGCACTTTGGGAGG A G GTF2H2B Ensembl:ENSG00000226259 Pseudogene intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1204707272 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8267857,Human_RBP_ID_8894354,Human_RBP_ID_10232211,Human_RBP_ID_18170789 RMVar_hsa_circ_89196,RMVar_hsa_circ_101850,RMVar_hsa_circ_86263,RMVar_hsa_circ_232084,RMVar_hsa_circ_232085,RMVar_hsa_circ_121875,RMVar_hsa_circ_232086,RMVar_hsa_circ_232088,RMVar_hsa_circ_115485,RMVar_hsa_circ_99671,RMVar_hsa_circ_83229,RMVar_hsa_circ_232103,RMVar_hsa_circ_232104,RMVar_hsa_circ_232105,RMVar_hsa_circ_83174,RMVar_hsa_circ_87382,RMVar_hsa_circ_232110,RMVar_hsa_circ_232111,RMVar_hsa_circ_11078,RMVar_hsa_circ_232130,RMVar_hsa_circ_269118,RMVar_hsa_circ_324794,RMVar_hsa_circ_377945,RMVar_hsa_circ_21254,RMVar_hsa_circ_326079,RMVar_hsa_circ_232133 20850 RMVar_ID_20850 Human_SNP_ID_236073430 A-to-I Human chr5 + 70439341 70439341 70439341 TAATGCTAGCACTTTGGGAGGCTCAGGTGGGCAGATCACTTGAGCCCAGGAGTTCGAGATCAGCA TAATGCTAGCACTTTGGGAGGCTCAGGTGGGCCGATCACTTGAGCCCAGGAGTTCGAGATCAGCA A C GTF2H2B Ensembl:ENSG00000226259 Pseudogene intron GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank;Bronchiolar epithelium,BEP2D cell line - 29129909,30559470,31158229 RNA-Seq:(High) rs1375922868 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89196,RMVar_hsa_circ_101850,RMVar_hsa_circ_86263,RMVar_hsa_circ_232084,RMVar_hsa_circ_232085,RMVar_hsa_circ_121875,RMVar_hsa_circ_232086,RMVar_hsa_circ_232088,RMVar_hsa_circ_115485,RMVar_hsa_circ_99671,RMVar_hsa_circ_83229,RMVar_hsa_circ_232103,RMVar_hsa_circ_232104,RMVar_hsa_circ_232105,RMVar_hsa_circ_83174,RMVar_hsa_circ_87382,RMVar_hsa_circ_232110,RMVar_hsa_circ_232111,RMVar_hsa_circ_11078,RMVar_hsa_circ_232130,RMVar_hsa_circ_269118,RMVar_hsa_circ_324794,RMVar_hsa_circ_377945,RMVar_hsa_circ_21254,RMVar_hsa_circ_326079,RMVar_hsa_circ_232133 20851 RMVar_ID_20851 Human_SNP_ID_236073431 A-to-I Human chr5 + 70439341 70439341 70439341 TAATGCTAGCACTTTGGGAGGCTCAGGTGGGCAGATCACTTGAGCCCAGGAGTTCGAGATCAGCA TAATGCTAGCACTTTGGGAGGCTCAGGTGGGCGGATCACTTGAGCCCAGGAGTTCGAGATCAGCA A G GTF2H2B Ensembl:ENSG00000226259 Pseudogene intron GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank;Bronchiolar epithelium,BEP2D cell line - 29129909,30559470,31158229 RNA-Seq:(High) rs1375922868 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89196,RMVar_hsa_circ_101850,RMVar_hsa_circ_86263,RMVar_hsa_circ_232084,RMVar_hsa_circ_232085,RMVar_hsa_circ_121875,RMVar_hsa_circ_232086,RMVar_hsa_circ_232088,RMVar_hsa_circ_115485,RMVar_hsa_circ_99671,RMVar_hsa_circ_83229,RMVar_hsa_circ_232103,RMVar_hsa_circ_232104,RMVar_hsa_circ_232105,RMVar_hsa_circ_83174,RMVar_hsa_circ_87382,RMVar_hsa_circ_232110,RMVar_hsa_circ_232111,RMVar_hsa_circ_11078,RMVar_hsa_circ_232130,RMVar_hsa_circ_269118,RMVar_hsa_circ_324794,RMVar_hsa_circ_377945,RMVar_hsa_circ_21254,RMVar_hsa_circ_326079,RMVar_hsa_circ_232133 20852 RMVar_ID_20852 Human_SNP_ID_236107333 A-to-I Human chr5 + 70955664 70955664 70955664 AAAATTAGCTCGGCATGGTGGTGGGCGCCTGTAATCCCAGCTACTGGAGAGGCTGAAGCATGAGA AAAATTAGCTCGGCATGGTGGTGGGCGCCTGTCATCCCAGCTACTGGAGAGGCTGAAGCATGAGA A C RF00017-462 RNACentral:URS00009A2CEE SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs212207 Functional Loss SNV dbSNP153 33..33 33 - - - 20853 RMVar_ID_20853 Human_SNP_ID_236107334 A-to-I Human chr5 + 70955664 70955664 70955664 AAAATTAGCTCGGCATGGTGGTGGGCGCCTGTAATCCCAGCTACTGGAGAGGCTGAAGCATGAGA AAAATTAGCTCGGCATGGTGGTGGGCGCCTGTGATCCCAGCTACTGGAGAGGCTGAAGCATGAGA A G RF00017-462 RNACentral:URS00009A2CEE SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs212207 Functional Loss SNV dbSNP153 33..33 33 - - - 20854 RMVar_ID_20854 Human_SNP_ID_236110049 A-to-I Human chr5 + 70978287 70978287 70978287 GATCCTACCAGCCTCCTGAGTAGCTGGGGACTATAGGTGCACACCATCATACTTGGCTAATTTTT GATCCTACCAGCCTCCTGAGTAGCTGGGGACTCTAGGTGCACACCATCATACTTGGCTAATTTTT A C RF00017-462 RNACentral:URS00009A2CEE SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1449867283 Functional Loss SNV dbSNP153 33..33 33 - - - 20855 RMVar_ID_20855 Human_SNP_ID_236114953 A-to-I Human chr5 - 71028255 71028255 71028255 CTTTTGTTTTGTTTTTTTTTTTTTTTTGAGACAGAGTCTCGCTCTGTCACCCAGGCTGGAGTGCA CTTTTGTTTTGTTTTTTTTTTTTTTTTGAGACTGAGTCTCGCTCTGTCACCCAGGCTGGAGTGCA T A RF00017-4486,RF00017-4685 RNACentral:URS000090F764,RNACentral:URS0000985E23 SRP RNA,SRP RNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1220352970 Functional Loss SNV dbSNP153 33..33 33 - - - 20856 RMVar_ID_20856 Human_SNP_ID_236115764 A-to-I Human chr5 - 71035042 71035042 71035042 GGGAGGCTGAGGCAGGAGAATCGCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCCAAGATTGTG GGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGGGAGGCGGAGGTTGCAGTGAGCCAAGATTGTG T C GTF2H2 Ensembl:ENSG00000145736 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1383639471 Functional Loss SNV dbSNP153 33..33 33 - - - 20857 RMVar_ID_20857 Human_SNP_ID_236171746 A-to-I Human chr5 + 71471389 71471389 71471389 GTCTTGAACTCTTGACCTCTGGTGATTCACCCACCTTGGCCTCCCACCAAGTGCTGGAATTACAG GTCTTGAACTCTTGACCTCTGGTGATTCACCCCCCTTGGCCTCCCACCAAGTGCTGGAATTACAG A C BDP1 Ensembl:ENSG00000145734 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1179246765 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8621137,Human_RBP_ID_15502795 RMVar_hsa_circ_53964,RMVar_hsa_circ_32333,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_232196,RMVar_hsa_circ_66041,RMVar_hsa_circ_232197,RMVar_hsa_circ_24808,RMVar_hsa_circ_37593,RMVar_hsa_circ_232198,RMVar_hsa_circ_232199,RMVar_hsa_circ_85338 20858 RMVar_ID_20858 Human_SNP_ID_236178604 A-to-I Human chr5 + 71497815 71497815 71497815 TGTTTGTTTTTTCTGAGACAGGGTCTTGCTCTATTGCCCAGGCAACAGAGTCCAGGAGTGCAATG TGTTTGTTTTTTCTGAGACAGGGTCTTGCTCTGTTGCCCAGGCAACAGAGTCCAGGAGTGCAATG A G BDP1 Ensembl:ENSG00000145734 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1187294951 Functional Loss SNV dbSNP153 33..33 33 - - - 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_66041,RMVar_hsa_circ_232197,RMVar_hsa_circ_24808,RMVar_hsa_circ_232198,RMVar_hsa_circ_127599,RMVar_hsa_circ_232199,RMVar_hsa_circ_85338,RMVar_hsa_circ_232200,RMVar_hsa_circ_102605,RMVar_hsa_circ_232206,RMVar_hsa_circ_312415,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_232203 20859 RMVar_ID_20859 Human_SNP_ID_236179467 A-to-I Human chr5 + 71501012 71501012 71501012 CCAGCTACTCAGGAGGCTGAGGTGGGAGGATCACCTGAGCCTTGGGGGTCAAGGCTGCAGTGAGC CCAGCTACTCAGGAGGCTGAGGTGGGAGGATCTCCTGAGCCTTGGGGGTCAAGGCTGCAGTGAGC A T BDP1 Ensembl:ENSG00000145734 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs763082338 Functional Loss SNV dbSNP153 33..33 33 - - - 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_66041,RMVar_hsa_circ_232197,RMVar_hsa_circ_24808,RMVar_hsa_circ_232198,RMVar_hsa_circ_127599,RMVar_hsa_circ_232199,RMVar_hsa_circ_85338,RMVar_hsa_circ_232200,RMVar_hsa_circ_102605,RMVar_hsa_circ_232206,RMVar_hsa_circ_312415,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_232203 20860 RMVar_ID_20860 Human_SNP_ID_236184904 A-to-I Human chr5 + 71520951 71520947 71520952 TGGCTCACACCTGTAATCCCAGCGCTCTGGGAAACCAAGGCGGGCGAATCACCTGAGTTCGGGAG TGGCTCACACCTGTAATCCCAGCGCTCTG_____CCAAGGCGGGCGAATCACCTGAGTTCGGGAG GGGAAA G BDP1 Ensembl:ENSG00000145734 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1401389760 Functional Loss DEL dbSNP153 30..34 33 - - - 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_232201,RMVar_hsa_circ_377680,RMVar_hsa_circ_103416,RMVar_hsa_circ_232207,RMVar_hsa_circ_66444,RMVar_hsa_circ_68213,RMVar_hsa_circ_232213,RMVar_hsa_circ_232212,RMVar_hsa_circ_77784,RMVar_hsa_circ_370822,RMVar_hsa_circ_232222,RMVar_hsa_circ_232223,RMVar_hsa_circ_22604,RMVar_hsa_circ_48625,RMVar_hsa_circ_66478,RMVar_hsa_circ_232235,RMVar_hsa_circ_232236,RMVar_hsa_circ_315904,RMVar_hsa_circ_232237,RMVar_hsa_circ_40018 20861 RMVar_ID_20861 Human_SNP_ID_236184907 A-to-I Human chr5 + 71520955 71520955 71520955 TCACACCTGTAATCCCAGCGCTCTGGGAAACCAAGGCGGGCGAATCACCTGAGTTCGGGAGTTTG TCACACCTGTAATCCCAGCGCTCTGGGAAACCGAGGCGGGCGAATCACCTGAGTTCGGGAGTTTG A G BDP1 Ensembl:ENSG00000145734 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1301023334 Functional Loss SNV dbSNP153 33..33 33 - - - 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_232201,RMVar_hsa_circ_377680,RMVar_hsa_circ_103416,RMVar_hsa_circ_232207,RMVar_hsa_circ_66444,RMVar_hsa_circ_68213,RMVar_hsa_circ_232213,RMVar_hsa_circ_232212,RMVar_hsa_circ_77784,RMVar_hsa_circ_370822,RMVar_hsa_circ_232222,RMVar_hsa_circ_232223,RMVar_hsa_circ_22604,RMVar_hsa_circ_48625,RMVar_hsa_circ_66478,RMVar_hsa_circ_232235,RMVar_hsa_circ_232236,RMVar_hsa_circ_315904,RMVar_hsa_circ_232237,RMVar_hsa_circ_40018 20862 RMVar_ID_20862 Human_SNP_ID_236185054 A-to-I Human chr5 + 71521454 71521454 71521454 AGCTGGGACTTCAGGCATGCACGACCATGCCCAGCTAATTTTTTATTTTTGGTAGAGATGGGGTT AGCTGGGACTTCAGGCATGCACGACCATGCCCCGCTAATTTTTTATTTTTGGTAGAGATGGGGTT A C BDP1 Ensembl:ENSG00000145734 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1239201873 Functional Loss SNV dbSNP153 33..33 33 - - - 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_232201,RMVar_hsa_circ_377680,RMVar_hsa_circ_103416,RMVar_hsa_circ_232207,RMVar_hsa_circ_66444,RMVar_hsa_circ_68213,RMVar_hsa_circ_232213,RMVar_hsa_circ_232212,RMVar_hsa_circ_77784,RMVar_hsa_circ_370822,RMVar_hsa_circ_232222,RMVar_hsa_circ_232223,RMVar_hsa_circ_22604,RMVar_hsa_circ_48625,RMVar_hsa_circ_66478,RMVar_hsa_circ_232235,RMVar_hsa_circ_232236,RMVar_hsa_circ_315904,RMVar_hsa_circ_232237,RMVar_hsa_circ_40018 20863 RMVar_ID_20863 Human_SNP_ID_236187569 A-to-I Human chr5 + 71529568 71529568 71529568 AATAAATTAGCAAGGTGTGTTGGTGCGTATCTATAATCCCAGCTACTCAGAAGGCTGAGTGGGGA AATAAATTAGCAAGGTGTGTTGGTGCGTATCTGTAATCCCAGCTACTCAGAAGGCTGAGTGGGGA A G BDP1 Ensembl:ENSG00000145734 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs76836990 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25914233 RMVar_hsa_circ_116406,RMVar_hsa_circ_232198,RMVar_hsa_circ_102605,RMVar_hsa_circ_111876,RMVar_hsa_circ_232201,RMVar_hsa_circ_377680,RMVar_hsa_circ_66444,RMVar_hsa_circ_68213,RMVar_hsa_circ_7040,RMVar_hsa_circ_232213,RMVar_hsa_circ_232212,RMVar_hsa_circ_77784,RMVar_hsa_circ_370822,RMVar_hsa_circ_232222,RMVar_hsa_circ_232223,RMVar_hsa_circ_232235,RMVar_hsa_circ_232236,RMVar_hsa_circ_315904,RMVar_hsa_circ_40018,RMVar_hsa_circ_266411,RMVar_hsa_circ_284692,RMVar_hsa_circ_339655,RMVar_hsa_circ_80020,RMVar_hsa_circ_66695,RMVar_hsa_circ_232239,RMVar_hsa_circ_232240,RMVar_hsa_circ_232241,RMVar_hsa_circ_232238 20864 RMVar_ID_20864 Human_SNP_ID_236187787 A-to-I Human chr5 + 71530518 71530518 71530518 TGCCAACCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCTACCGTGCCTGGCCTATTGTT TGCCAACCTCAGCCTCCCAAAGTGCTGGGATTGCAGGCATGAGCTACCGTGCCTGGCCTATTGTT A G BDP1 Ensembl:ENSG00000145734 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs747989732 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116406,RMVar_hsa_circ_232198,RMVar_hsa_circ_102605,RMVar_hsa_circ_111876,RMVar_hsa_circ_232201,RMVar_hsa_circ_377680,RMVar_hsa_circ_66444,RMVar_hsa_circ_68213,RMVar_hsa_circ_7040,RMVar_hsa_circ_232213,RMVar_hsa_circ_232212,RMVar_hsa_circ_77784,RMVar_hsa_circ_370822,RMVar_hsa_circ_232222,RMVar_hsa_circ_232223,RMVar_hsa_circ_232235,RMVar_hsa_circ_232236,RMVar_hsa_circ_315904,RMVar_hsa_circ_40018,RMVar_hsa_circ_266411,RMVar_hsa_circ_284692,RMVar_hsa_circ_339655,RMVar_hsa_circ_80020,RMVar_hsa_circ_66695,RMVar_hsa_circ_232239,RMVar_hsa_circ_232240,RMVar_hsa_circ_232241,RMVar_hsa_circ_232238 20865 RMVar_ID_20865 Human_SNP_ID_236187828 A-to-I Human chr5 + 71530652 71530652 71530652 AGCGACCCTCACACCTCAGCCTCCGAGTAGCTAGAACTACAGGCATGTGCCCCCGTGCTCACTTG AGCGACCCTCACACCTCAGCCTCCGAGTAGCTGGAACTACAGGCATGTGCCCCCGTGCTCACTTG A G BDP1 Ensembl:ENSG00000145734 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1388538599 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15504035 RMVar_hsa_circ_116406,RMVar_hsa_circ_232198,RMVar_hsa_circ_102605,RMVar_hsa_circ_111876,RMVar_hsa_circ_232201,RMVar_hsa_circ_377680,RMVar_hsa_circ_66444,RMVar_hsa_circ_68213,RMVar_hsa_circ_7040,RMVar_hsa_circ_232213,RMVar_hsa_circ_232212,RMVar_hsa_circ_77784,RMVar_hsa_circ_370822,RMVar_hsa_circ_232222,RMVar_hsa_circ_232223,RMVar_hsa_circ_232235,RMVar_hsa_circ_232236,RMVar_hsa_circ_315904,RMVar_hsa_circ_40018,RMVar_hsa_circ_266411,RMVar_hsa_circ_284692,RMVar_hsa_circ_339655,RMVar_hsa_circ_80020,RMVar_hsa_circ_66695,RMVar_hsa_circ_232239,RMVar_hsa_circ_232240,RMVar_hsa_circ_232241,RMVar_hsa_circ_232238 20866 RMVar_ID_20866 Human_SNP_ID_236191557 A-to-I Human chr5 + 71545401 71545401 71545401 TTGCCCAGGCAAGAGTGCAGTGGTATGATCTCAGCTCACTGCAACCTCTGCCACCCAGATTCAAC TTGCCCAGGCAAGAGTGCAGTGGTATGATCTCGGCTCACTGCAACCTCTGCCACCCAGATTCAAC A G BDP1 Ensembl:ENSG00000145734 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935315259 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116406,RMVar_hsa_circ_232198,RMVar_hsa_circ_111876,RMVar_hsa_circ_7040,RMVar_hsa_circ_232212,RMVar_hsa_circ_232236,RMVar_hsa_circ_315904,RMVar_hsa_circ_339655,RMVar_hsa_circ_68280,RMVar_hsa_circ_232240,RMVar_hsa_circ_232241,RMVar_hsa_circ_232242,RMVar_hsa_circ_310333,RMVar_hsa_circ_269326,RMVar_hsa_circ_46036,RMVar_hsa_circ_35233,RMVar_hsa_circ_232247,RMVar_hsa_circ_72722,RMVar_hsa_circ_299022,RMVar_hsa_circ_232249,RMVar_hsa_circ_59093,RMVar_hsa_circ_232250,RMVar_hsa_circ_378576,RMVar_hsa_circ_232248,RMVar_hsa_circ_356895 20867 RMVar_ID_20867 Human_SNP_ID_236191790 A-to-I Human chr5 + 71546454 71546454 71546454 CAGCCTGGCAAACAAGGTGAAACCCCATCACTACAAAAATACAAAAATTAGCCAGTCGTGGTGGC CAGCCTGGCAAACAAGGTGAAACCCCATCACTGCAAAAATACAAAAATTAGCCAGTCGTGGTGGC A G BDP1 Ensembl:ENSG00000145734 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1420446333 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7040,RMVar_hsa_circ_232236,RMVar_hsa_circ_315904,RMVar_hsa_circ_339655,RMVar_hsa_circ_68280,RMVar_hsa_circ_232240,RMVar_hsa_circ_232241,RMVar_hsa_circ_232242,RMVar_hsa_circ_310333,RMVar_hsa_circ_269326,RMVar_hsa_circ_46036,RMVar_hsa_circ_35233,RMVar_hsa_circ_232247,RMVar_hsa_circ_72722,RMVar_hsa_circ_299022,RMVar_hsa_circ_232249,RMVar_hsa_circ_59093,RMVar_hsa_circ_232250,RMVar_hsa_circ_378576,RMVar_hsa_circ_232248,RMVar_hsa_circ_356895 20868 RMVar_ID_20868 Human_SNP_ID_236192212 A-to-I Human chr5 + 71547837 71547837 71547837 GGGCATGGTGGTGTGTGCCTGTAGTCCCAGCTACTCAGGAGACTGAGGCAGGAGAATTGCTCGGA GGGCATGGTGGTGTGTGCCTGTAGTCCCAGCTGCTCAGGAGACTGAGGCAGGAGAATTGCTCGGA A G BDP1 Ensembl:ENSG00000145734 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1410211598 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7040,RMVar_hsa_circ_232236,RMVar_hsa_circ_315904,RMVar_hsa_circ_339655,RMVar_hsa_circ_68280,RMVar_hsa_circ_232240,RMVar_hsa_circ_232241,RMVar_hsa_circ_232242,RMVar_hsa_circ_310333,RMVar_hsa_circ_269326,RMVar_hsa_circ_46036,RMVar_hsa_circ_35233,RMVar_hsa_circ_232247,RMVar_hsa_circ_72722,RMVar_hsa_circ_299022,RMVar_hsa_circ_232249,RMVar_hsa_circ_59093,RMVar_hsa_circ_232250,RMVar_hsa_circ_378576,RMVar_hsa_circ_232248,RMVar_hsa_circ_356895 20869 RMVar_ID_20869 Human_SNP_ID_236196590 A-to-I Human chr5 + 71563265 71563265 71563265 CATCCCCTGGGTTCAAGTGATTCTCCTGTCTCAGCTTCTCGATTAGCTGAGCTTACAGATGCATG CATCCCCTGGGTTCAAGTGATTCTCCTGTCTCGGCTTCTCGATTAGCTGAGCTTACAGATGCATG A G BDP1 Ensembl:ENSG00000145734 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1459680277 Functional Loss SNV dbSNP153 33..33 33 - - - 20870 RMVar_ID_20870 Human_SNP_ID_236196700 A-to-I Human chr5 + 71563734 71563734 71563734 GAGGAGTTTGAGACCAGCCTGGCCAACATGGCAAAACCCCATCTCTACCAAAATACAAAATTTAA GAGGAGTTTGAGACCAGCCTGGCCAACATGGCGAAACCCCATCTCTACCAAAATACAAAATTTAA A G BDP1 Ensembl:ENSG00000145734 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1408932250 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18051939 20871 RMVar_ID_20871 Human_SNP_ID_236203476 A-to-I Human chr5 + 71591806 71591806 71591806 AAACAGTCTTGCTCTGTCACCCAGGCTGGAGTACAATGGCACGATCCTAGTTCACTGCAGCTTCA AAACAGTCTTGCTCTGTCACCCAGGCTGGAGTGCAATGGCACGATCCTAGTTCACTGCAGCTTCA A G MCCC2 Ensembl:ENSG00000131844 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs373849447 Functional Loss SNV dbSNP153 33..33 33 - - - 20872 RMVar_ID_20872 Human_SNP_ID_236218806 A-to-I Human chr5 + 71653616 71653616 71653616 TCACACTTATAATCCCAGCATTTTGAGAGGCCAGGGCGGGCAGATTGCTTGAGCCCAGGAGTTCG TCACACTTATAATCCCAGCATTTTGAGAGGCCGGGGCGGGCAGATTGCTTGAGCCCAGGAGTTCG A G MCCC2 Ensembl:ENSG00000131844 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs761975256 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87157,RMVar_hsa_circ_232267 20873 RMVar_ID_20873 Human_SNP_ID_236219143 A-to-I Human chr5 + 71655099 71655099 71655099 CAGGTGATCCACCCGCCTCGGCTTCCCAAAGTACTGGGATTACAGGCATGAGCCACTGCACCTGG CAGGTGATCCACCCGCCTCGGCTTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGCACCTGG A G MCCC2 Ensembl:ENSG00000131844 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs900176963 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87157,RMVar_hsa_circ_232267 20874 RMVar_ID_20874 Human_SNP_ID_236219144 A-to-I Human chr5 + 71655099 71655099 71655099 CAGGTGATCCACCCGCCTCGGCTTCCCAAAGTACTGGGATTACAGGCATGAGCCACTGCACCTGG CAGGTGATCCACCCGCCTCGGCTTCCCAAAGTTCTGGGATTACAGGCATGAGCCACTGCACCTGG A T MCCC2 Ensembl:ENSG00000131844 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs900176963 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87157,RMVar_hsa_circ_232267 20875 RMVar_ID_20875 Human_SNP_ID_236357685 A-to-I Human chr5 - 72220373 72220373 72220373 GGGATTACAGGTGCATACCACCACACCTTTCTAATTTTTGCATTTTTAGTAGAGATGGGGTTTCA GGGATTACAGGTGCATACCACCACACCTTTCTGATTTTTGCATTTTTAGTAGAGATGGGGTTTCA T C MRPS27 Ensembl:ENSG00000113048 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1337831780 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_166734,Human_RBP_ID_1042464,Human_RBP_ID_7465535,Human_RBP_ID_8135515,Human_RBP_ID_17301145,Human_RBP_ID_17414456,Human_RBP_ID_17531184,Human_RBP_ID_18052170 20876 RMVar_ID_20876 Human_SNP_ID_236357693 A-to-I Human chr5 - 72220399 72220399 72220399 TCCTGCCTCGGCCTCCTTTAGTAGGTGGGATTACAGGTGCATACCACCACACCTTTCTAATTTTT TCCTGCCTCGGCCTCCTTTAGTAGGTGGGATTGCAGGTGCATACCACCACACCTTTCTAATTTTT T C MRPS27 Ensembl:ENSG00000113048 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs933052039 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23194094 20877 RMVar_ID_20877 Human_SNP_ID_236357714 A-to-I Human chr5 - 72220475 72220468 72220475 TTCTGTCACCCAGGCTGGAGTGCAGTGGCGCAATCTTGGCTCACTGCAACCTCCGACTCCCAGGT TTCTGTCACCCAGGCTGGAGTGCAGTGGCGCA_______CTCACTGCAACCTCCGACTCCCAGGT GCCAAGAT G MRPS27 Ensembl:ENSG00000113048 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs952178856 Functional Loss DEL dbSNP153 33..39 33 - - - 20878 RMVar_ID_20878 Human_SNP_ID_236357715 A-to-I Human chr5 - 72220475 72220475 72220475 TTCTGTCACCCAGGCTGGAGTGCAGTGGCGCAATCTTGGCTCACTGCAACCTCCGACTCCCAGGT TTCTGTCACCCAGGCTGGAGTGCAGTGGCGCAGTCTTGGCTCACTGCAACCTCCGACTCCCAGGT T C MRPS27 Ensembl:ENSG00000113048 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1006340639 Functional Loss SNV dbSNP153 33..33 33 - - - 20879 RMVar_ID_20879 Human_SNP_ID_236357939 A-to-I Human chr5 - 72221260 72221260 72221260 GGGCCACTAGAATGAGGACTAAACTACGAGTCAGCAAACTTTTGTTCAAATCTAAAGTCAGTCAC GGGCCACTAGAATGAGGACTAAACTACGAGTCCGCAAACTTTTGTTCAAATCTAAAGTCAGTCAC T G MRPS27 Ensembl:ENSG00000113048 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1403167966 Functional Loss SNV dbSNP153 33..33 33 - - - 20880 RMVar_ID_20880 Human_SNP_ID_236380208 A-to-I Human chr5 - 72318755 72318755 72318755 GGTTTCGTTCTTGTTGCCCAGGTTAGAGTGCAATGGCACGATCTCGGCTTACTGCAGCCTCTGCC GGTTTCGTTCTTGTTGCCCAGGTTAGAGTGCACTGGCACGATCTCGGCTTACTGCAGCCTCTGCC T G MRPS27 Ensembl:ENSG00000113048 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs865919723 Functional Loss SNV dbSNP153 33..33 33 - - - 20881 RMVar_ID_20881 Human_SNP_ID_236506178 A-to-I Human chr5 + 72862848 72862848 72862848 TTTTGTATTTTTAGTAGAGACAGAGTTTCACCATGTTGGACAGGCTGGTCTTGAACTCCTGGACT TTTTGTATTTTTAGTAGAGACAGAGTTTCACCGTGTTGGACAGGCTGGTCTTGAACTCCTGGACT A G TNPO1 Ensembl:ENSG00000083312 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs528912811 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67841,RMVar_hsa_circ_232317,RMVar_hsa_circ_111249,RMVar_hsa_circ_113732,RMVar_hsa_circ_232313,RMVar_hsa_circ_318015,RMVar_hsa_circ_71533,RMVar_hsa_circ_71542,RMVar_hsa_circ_232315,RMVar_hsa_circ_44267,RMVar_hsa_circ_87992,RMVar_hsa_circ_94224,RMVar_hsa_circ_232319,RMVar_hsa_circ_77211,RMVar_hsa_circ_232318,RMVar_hsa_circ_275788,RMVar_hsa_circ_311388,RMVar_hsa_circ_334685,RMVar_hsa_circ_232316,RMVar_hsa_circ_344318,RMVar_hsa_circ_321205,RMVar_hsa_circ_295973,RMVar_hsa_circ_274938,RMVar_hsa_circ_52640,RMVar_hsa_circ_232324,RMVar_hsa_circ_26926,RMVar_hsa_circ_45831,RMVar_hsa_circ_59485,RMVar_hsa_circ_28505,RMVar_hsa_circ_232321,RMVar_hsa_circ_2904,RMVar_hsa_circ_232322,RMVar_hsa_circ_232320,RMVar_hsa_circ_295496,RMVar_hsa_circ_322951,RMVar_hsa_circ_341325,RMVar_hsa_circ_232325,RMVar_hsa_circ_344091,RMVar_hsa_circ_328586,RMVar_hsa_circ_317188,RMVar_hsa_circ_317517,RMVar_hsa_circ_302256,RMVar_hsa_circ_290962,RMVar_hsa_circ_292671,RMVar_hsa_circ_274231,RMVar_hsa_circ_232326,RMVar_hsa_circ_232330,RMVar_hsa_circ_38203,RMVar_hsa_circ_52311,RMVar_hsa_circ_232331,RMVar_hsa_circ_232332,RMVar_hsa_circ_232328,RMVar_hsa_circ_232329,RMVar_hsa_circ_232327 20882 RMVar_ID_20882 Human_SNP_ID_236506453 A-to-I Human chr5 + 72863591 72863591 72863591 AGAGACCAGCCTGGCCAACATGGTAAAACCCCATCTCTACTGAAATACAAAAATTAGCCAGGCAT AGAGACCAGCCTGGCCAACATGGTAAAACCCCGTCTCTACTGAAATACAAAAATTAGCCAGGCAT A G TNPO1 Ensembl:ENSG00000083312 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs896271747 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67841,RMVar_hsa_circ_232317,RMVar_hsa_circ_111249,RMVar_hsa_circ_113732,RMVar_hsa_circ_232313,RMVar_hsa_circ_318015,RMVar_hsa_circ_71533,RMVar_hsa_circ_71542,RMVar_hsa_circ_232315,RMVar_hsa_circ_44267,RMVar_hsa_circ_87992,RMVar_hsa_circ_94224,RMVar_hsa_circ_232319,RMVar_hsa_circ_77211,RMVar_hsa_circ_232318,RMVar_hsa_circ_275788,RMVar_hsa_circ_311388,RMVar_hsa_circ_334685,RMVar_hsa_circ_232316,RMVar_hsa_circ_344318,RMVar_hsa_circ_321205,RMVar_hsa_circ_295973,RMVar_hsa_circ_274938,RMVar_hsa_circ_52640,RMVar_hsa_circ_232324,RMVar_hsa_circ_26926,RMVar_hsa_circ_45831,RMVar_hsa_circ_59485,RMVar_hsa_circ_28505,RMVar_hsa_circ_232321,RMVar_hsa_circ_2904,RMVar_hsa_circ_232322,RMVar_hsa_circ_232320,RMVar_hsa_circ_295496,RMVar_hsa_circ_322951,RMVar_hsa_circ_341325,RMVar_hsa_circ_232325,RMVar_hsa_circ_344091,RMVar_hsa_circ_328586,RMVar_hsa_circ_317188,RMVar_hsa_circ_317517,RMVar_hsa_circ_302256,RMVar_hsa_circ_290962,RMVar_hsa_circ_292671,RMVar_hsa_circ_274231,RMVar_hsa_circ_232326,RMVar_hsa_circ_232330,RMVar_hsa_circ_38203,RMVar_hsa_circ_52311,RMVar_hsa_circ_232331,RMVar_hsa_circ_232332,RMVar_hsa_circ_232328,RMVar_hsa_circ_232329,RMVar_hsa_circ_232327 20883 RMVar_ID_20883 Human_SNP_ID_236506722 A-to-I Human chr5 + 72864632 72864631 72864633 TGTAAGTAACTTTTTTTTCCTTTTTTTGAGACAGAGTTTTGCTTTGTCACCCAGGCTGGAGTGCA TGTAAGTAACTTTTTTTTCCTTTTTTTGAGAC__AGTTTTGCTTTGTCACCCAGGCTGGAGTGCA CAG C TNPO1 Ensembl:ENSG00000083312 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1433476537 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_67841,RMVar_hsa_circ_232317,RMVar_hsa_circ_111249,RMVar_hsa_circ_113732,RMVar_hsa_circ_232313,RMVar_hsa_circ_318015,RMVar_hsa_circ_71533,RMVar_hsa_circ_71542,RMVar_hsa_circ_232315,RMVar_hsa_circ_44267,RMVar_hsa_circ_87992,RMVar_hsa_circ_94224,RMVar_hsa_circ_232319,RMVar_hsa_circ_77211,RMVar_hsa_circ_232318,RMVar_hsa_circ_275788,RMVar_hsa_circ_311388,RMVar_hsa_circ_334685,RMVar_hsa_circ_232316,RMVar_hsa_circ_344318,RMVar_hsa_circ_321205,RMVar_hsa_circ_295973,RMVar_hsa_circ_274938,RMVar_hsa_circ_52640,RMVar_hsa_circ_232324,RMVar_hsa_circ_26926,RMVar_hsa_circ_45831,RMVar_hsa_circ_59485,RMVar_hsa_circ_28505,RMVar_hsa_circ_232321,RMVar_hsa_circ_2904,RMVar_hsa_circ_232322,RMVar_hsa_circ_232320,RMVar_hsa_circ_295496,RMVar_hsa_circ_322951,RMVar_hsa_circ_341325,RMVar_hsa_circ_232325,RMVar_hsa_circ_344091,RMVar_hsa_circ_328586,RMVar_hsa_circ_317188,RMVar_hsa_circ_317517,RMVar_hsa_circ_302256,RMVar_hsa_circ_290962,RMVar_hsa_circ_292671,RMVar_hsa_circ_274231,RMVar_hsa_circ_232326,RMVar_hsa_circ_232330,RMVar_hsa_circ_38203,RMVar_hsa_circ_52311,RMVar_hsa_circ_232331,RMVar_hsa_circ_232332,RMVar_hsa_circ_232328,RMVar_hsa_circ_232329,RMVar_hsa_circ_232327 20884 RMVar_ID_20884 Human_SNP_ID_236506889 A-to-I Human chr5 + 72865271 72865271 72865271 TGAGACCAGCCTGGCCAACACAGTGAAACCCCATCTCTACAAAAAATACAAAACTTAGCCGGGCA TGAGACCAGCCTGGCCAACACAGTGAAACCCCGTCTCTACAAAAAATACAAAACTTAGCCGGGCA A G TNPO1 Ensembl:ENSG00000083312 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1304692172 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67841,RMVar_hsa_circ_232317,RMVar_hsa_circ_111249,RMVar_hsa_circ_113732,RMVar_hsa_circ_232313,RMVar_hsa_circ_318015,RMVar_hsa_circ_71533,RMVar_hsa_circ_71542,RMVar_hsa_circ_232315,RMVar_hsa_circ_44267,RMVar_hsa_circ_87992,RMVar_hsa_circ_94224,RMVar_hsa_circ_232319,RMVar_hsa_circ_77211,RMVar_hsa_circ_232318,RMVar_hsa_circ_275788,RMVar_hsa_circ_311388,RMVar_hsa_circ_334685,RMVar_hsa_circ_232316,RMVar_hsa_circ_344318,RMVar_hsa_circ_321205,RMVar_hsa_circ_295973,RMVar_hsa_circ_274938,RMVar_hsa_circ_52640,RMVar_hsa_circ_232324,RMVar_hsa_circ_26926,RMVar_hsa_circ_45831,RMVar_hsa_circ_59485,RMVar_hsa_circ_28505,RMVar_hsa_circ_232321,RMVar_hsa_circ_2904,RMVar_hsa_circ_232322,RMVar_hsa_circ_232320,RMVar_hsa_circ_295496,RMVar_hsa_circ_322951,RMVar_hsa_circ_341325,RMVar_hsa_circ_232325,RMVar_hsa_circ_344091,RMVar_hsa_circ_328586,RMVar_hsa_circ_317188,RMVar_hsa_circ_317517,RMVar_hsa_circ_302256,RMVar_hsa_circ_290962,RMVar_hsa_circ_292671,RMVar_hsa_circ_274231,RMVar_hsa_circ_232326,RMVar_hsa_circ_232330,RMVar_hsa_circ_38203,RMVar_hsa_circ_52311,RMVar_hsa_circ_232331,RMVar_hsa_circ_232332,RMVar_hsa_circ_232328,RMVar_hsa_circ_232329,RMVar_hsa_circ_232327 20885 RMVar_ID_20885 Human_SNP_ID_236506890 A-to-I Human chr5 + 72865277 72865277 72865277 CAGCCTGGCCAACACAGTGAAACCCCATCTCTACAAAAAATACAAAACTTAGCCGGGCACAATGG CAGCCTGGCCAACACAGTGAAACCCCATCTCTGCAAAAAATACAAAACTTAGCCGGGCACAATGG A G TNPO1 Ensembl:ENSG00000083312 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs148767632 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67841,RMVar_hsa_circ_232317,RMVar_hsa_circ_111249,RMVar_hsa_circ_113732,RMVar_hsa_circ_232313,RMVar_hsa_circ_318015,RMVar_hsa_circ_71533,RMVar_hsa_circ_71542,RMVar_hsa_circ_232315,RMVar_hsa_circ_44267,RMVar_hsa_circ_87992,RMVar_hsa_circ_94224,RMVar_hsa_circ_232319,RMVar_hsa_circ_77211,RMVar_hsa_circ_232318,RMVar_hsa_circ_275788,RMVar_hsa_circ_311388,RMVar_hsa_circ_334685,RMVar_hsa_circ_232316,RMVar_hsa_circ_344318,RMVar_hsa_circ_321205,RMVar_hsa_circ_295973,RMVar_hsa_circ_274938,RMVar_hsa_circ_52640,RMVar_hsa_circ_232324,RMVar_hsa_circ_26926,RMVar_hsa_circ_45831,RMVar_hsa_circ_59485,RMVar_hsa_circ_28505,RMVar_hsa_circ_232321,RMVar_hsa_circ_2904,RMVar_hsa_circ_232322,RMVar_hsa_circ_232320,RMVar_hsa_circ_295496,RMVar_hsa_circ_322951,RMVar_hsa_circ_341325,RMVar_hsa_circ_232325,RMVar_hsa_circ_344091,RMVar_hsa_circ_328586,RMVar_hsa_circ_317188,RMVar_hsa_circ_317517,RMVar_hsa_circ_302256,RMVar_hsa_circ_290962,RMVar_hsa_circ_292671,RMVar_hsa_circ_274231,RMVar_hsa_circ_232326,RMVar_hsa_circ_232330,RMVar_hsa_circ_38203,RMVar_hsa_circ_52311,RMVar_hsa_circ_232331,RMVar_hsa_circ_232332,RMVar_hsa_circ_232328,RMVar_hsa_circ_232329,RMVar_hsa_circ_232327 20886 RMVar_ID_20886 Human_SNP_ID_236507278 A-to-I Human chr5 + 72866607 72866607 72866607 GAGACCCCATCTGTACAAAAAATATAAAAATTAGCTGGGCATGGTGTCACACACCTGTGGTCCGA GAGACCCCATCTGTACAAAAAATATAAAAATTCGCTGGGCATGGTGTCACACACCTGTGGTCCGA A C TNPO1 Ensembl:ENSG00000083312 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1469118543 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2435,RMVar_hsa_circ_67841,RMVar_hsa_circ_232317,RMVar_hsa_circ_113732,RMVar_hsa_circ_232313,RMVar_hsa_circ_318015,RMVar_hsa_circ_71542,RMVar_hsa_circ_232315,RMVar_hsa_circ_44267,RMVar_hsa_circ_87992,RMVar_hsa_circ_94224,RMVar_hsa_circ_232319,RMVar_hsa_circ_77211,RMVar_hsa_circ_232318,RMVar_hsa_circ_275788,RMVar_hsa_circ_311388,RMVar_hsa_circ_334685,RMVar_hsa_circ_344318,RMVar_hsa_circ_321205,RMVar_hsa_circ_295973,RMVar_hsa_circ_52640,RMVar_hsa_circ_26926,RMVar_hsa_circ_45831,RMVar_hsa_circ_59485,RMVar_hsa_circ_28505,RMVar_hsa_circ_232321,RMVar_hsa_circ_2904,RMVar_hsa_circ_232320,RMVar_hsa_circ_295496,RMVar_hsa_circ_322951,RMVar_hsa_circ_341325,RMVar_hsa_circ_344091,RMVar_hsa_circ_328586,RMVar_hsa_circ_317188,RMVar_hsa_circ_317517,RMVar_hsa_circ_302256,RMVar_hsa_circ_290962,RMVar_hsa_circ_292671,RMVar_hsa_circ_232330,RMVar_hsa_circ_38203,RMVar_hsa_circ_52311,RMVar_hsa_circ_232331,RMVar_hsa_circ_232332,RMVar_hsa_circ_232328,RMVar_hsa_circ_232329,RMVar_hsa_circ_232327,RMVar_hsa_circ_46657,RMVar_hsa_circ_302712,RMVar_hsa_circ_337575,RMVar_hsa_circ_90298,RMVar_hsa_circ_38619,RMVar_hsa_circ_232333 20887 RMVar_ID_20887 Human_SNP_ID_236508024 A-to-I Human chr5 + 72868897 72868897 72868897 GGACGTGGTGGCGGGTGCTTGTAATCCTAGCTACTCGGGAGGCTGAGGCATGAGAATCACTTGAA GGACGTGGTGGCGGGTGCTTGTAATCCTAGCTTCTCGGGAGGCTGAGGCATGAGAATCACTTGAA A T TNPO1 Ensembl:ENSG00000083312 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs534050403 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2435,RMVar_hsa_circ_67841,RMVar_hsa_circ_232317,RMVar_hsa_circ_113732,RMVar_hsa_circ_232313,RMVar_hsa_circ_318015,RMVar_hsa_circ_71542,RMVar_hsa_circ_232315,RMVar_hsa_circ_44267,RMVar_hsa_circ_87992,RMVar_hsa_circ_94224,RMVar_hsa_circ_232319,RMVar_hsa_circ_77211,RMVar_hsa_circ_232318,RMVar_hsa_circ_275788,RMVar_hsa_circ_311388,RMVar_hsa_circ_334685,RMVar_hsa_circ_344318,RMVar_hsa_circ_321205,RMVar_hsa_circ_295973,RMVar_hsa_circ_52640,RMVar_hsa_circ_26926,RMVar_hsa_circ_45831,RMVar_hsa_circ_59485,RMVar_hsa_circ_28505,RMVar_hsa_circ_232321,RMVar_hsa_circ_2904,RMVar_hsa_circ_232320,RMVar_hsa_circ_295496,RMVar_hsa_circ_322951,RMVar_hsa_circ_341325,RMVar_hsa_circ_344091,RMVar_hsa_circ_328586,RMVar_hsa_circ_317188,RMVar_hsa_circ_317517,RMVar_hsa_circ_302256,RMVar_hsa_circ_290962,RMVar_hsa_circ_292671,RMVar_hsa_circ_232330,RMVar_hsa_circ_38203,RMVar_hsa_circ_52311,RMVar_hsa_circ_232331,RMVar_hsa_circ_232332,RMVar_hsa_circ_232328,RMVar_hsa_circ_232329,RMVar_hsa_circ_232327,RMVar_hsa_circ_46657,RMVar_hsa_circ_302712,RMVar_hsa_circ_337575,RMVar_hsa_circ_90298,RMVar_hsa_circ_38619,RMVar_hsa_circ_232333 20888 RMVar_ID_20888 Human_SNP_ID_236508395 A-to-I Human chr5 + 72870235 72870235 72870235 CACACTAGAGTGCAATGGCATTATCCCTGCTCACTGCAACCTCCACCTCCCAGGTTCAAGCGATT CACACTAGAGTGCAATGGCATTATCCCTGCTCCCTGCAACCTCCACCTCCCAGGTTCAAGCGATT A C TNPO1 Ensembl:ENSG00000083312 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1485336730 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2435,RMVar_hsa_circ_67841,RMVar_hsa_circ_232317,RMVar_hsa_circ_113732,RMVar_hsa_circ_232313,RMVar_hsa_circ_318015,RMVar_hsa_circ_71542,RMVar_hsa_circ_232315,RMVar_hsa_circ_44267,RMVar_hsa_circ_87992,RMVar_hsa_circ_94224,RMVar_hsa_circ_232319,RMVar_hsa_circ_77211,RMVar_hsa_circ_232318,RMVar_hsa_circ_275788,RMVar_hsa_circ_311388,RMVar_hsa_circ_334685,RMVar_hsa_circ_344318,RMVar_hsa_circ_321205,RMVar_hsa_circ_295973,RMVar_hsa_circ_52640,RMVar_hsa_circ_26926,RMVar_hsa_circ_45831,RMVar_hsa_circ_59485,RMVar_hsa_circ_28505,RMVar_hsa_circ_232321,RMVar_hsa_circ_2904,RMVar_hsa_circ_232320,RMVar_hsa_circ_295496,RMVar_hsa_circ_322951,RMVar_hsa_circ_341325,RMVar_hsa_circ_344091,RMVar_hsa_circ_328586,RMVar_hsa_circ_317188,RMVar_hsa_circ_317517,RMVar_hsa_circ_302256,RMVar_hsa_circ_290962,RMVar_hsa_circ_292671,RMVar_hsa_circ_232330,RMVar_hsa_circ_38203,RMVar_hsa_circ_52311,RMVar_hsa_circ_232331,RMVar_hsa_circ_232332,RMVar_hsa_circ_232328,RMVar_hsa_circ_232329,RMVar_hsa_circ_232327,RMVar_hsa_circ_46657,RMVar_hsa_circ_302712,RMVar_hsa_circ_337575,RMVar_hsa_circ_90298,RMVar_hsa_circ_38619,RMVar_hsa_circ_232333 20889 RMVar_ID_20889 Human_SNP_ID_236508396 A-to-I Human chr5 + 72870235 72870235 72870235 CACACTAGAGTGCAATGGCATTATCCCTGCTCACTGCAACCTCCACCTCCCAGGTTCAAGCGATT CACACTAGAGTGCAATGGCATTATCCCTGCTCTCTGCAACCTCCACCTCCCAGGTTCAAGCGATT A T TNPO1 Ensembl:ENSG00000083312 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1485336730 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2435,RMVar_hsa_circ_67841,RMVar_hsa_circ_232317,RMVar_hsa_circ_113732,RMVar_hsa_circ_232313,RMVar_hsa_circ_318015,RMVar_hsa_circ_71542,RMVar_hsa_circ_232315,RMVar_hsa_circ_44267,RMVar_hsa_circ_87992,RMVar_hsa_circ_94224,RMVar_hsa_circ_232319,RMVar_hsa_circ_77211,RMVar_hsa_circ_232318,RMVar_hsa_circ_275788,RMVar_hsa_circ_311388,RMVar_hsa_circ_334685,RMVar_hsa_circ_344318,RMVar_hsa_circ_321205,RMVar_hsa_circ_295973,RMVar_hsa_circ_52640,RMVar_hsa_circ_26926,RMVar_hsa_circ_45831,RMVar_hsa_circ_59485,RMVar_hsa_circ_28505,RMVar_hsa_circ_232321,RMVar_hsa_circ_2904,RMVar_hsa_circ_232320,RMVar_hsa_circ_295496,RMVar_hsa_circ_322951,RMVar_hsa_circ_341325,RMVar_hsa_circ_344091,RMVar_hsa_circ_328586,RMVar_hsa_circ_317188,RMVar_hsa_circ_317517,RMVar_hsa_circ_302256,RMVar_hsa_circ_290962,RMVar_hsa_circ_292671,RMVar_hsa_circ_232330,RMVar_hsa_circ_38203,RMVar_hsa_circ_52311,RMVar_hsa_circ_232331,RMVar_hsa_circ_232332,RMVar_hsa_circ_232328,RMVar_hsa_circ_232329,RMVar_hsa_circ_232327,RMVar_hsa_circ_46657,RMVar_hsa_circ_302712,RMVar_hsa_circ_337575,RMVar_hsa_circ_90298,RMVar_hsa_circ_38619,RMVar_hsa_circ_232333 20890 RMVar_ID_20890 Human_SNP_ID_236508640 A-to-I Human chr5 + 72871160 72871160 72871160 CACCAGGCCCGGCTAATTTTTGTATTTTTAGTAGAGGCAGGGTTTCACCATGTTGGCCAGGCTGG CACCAGGCCCGGCTAATTTTTGTATTTTTAGTGGAGGCAGGGTTTCACCATGTTGGCCAGGCTGG A G TNPO1 Ensembl:ENSG00000083312 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1188743056 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2435,RMVar_hsa_circ_67841,RMVar_hsa_circ_232317,RMVar_hsa_circ_113732,RMVar_hsa_circ_232313,RMVar_hsa_circ_318015,RMVar_hsa_circ_71542,RMVar_hsa_circ_232315,RMVar_hsa_circ_44267,RMVar_hsa_circ_87992,RMVar_hsa_circ_94224,RMVar_hsa_circ_232319,RMVar_hsa_circ_77211,RMVar_hsa_circ_232318,RMVar_hsa_circ_275788,RMVar_hsa_circ_311388,RMVar_hsa_circ_334685,RMVar_hsa_circ_344318,RMVar_hsa_circ_321205,RMVar_hsa_circ_295973,RMVar_hsa_circ_52640,RMVar_hsa_circ_26926,RMVar_hsa_circ_45831,RMVar_hsa_circ_59485,RMVar_hsa_circ_28505,RMVar_hsa_circ_232321,RMVar_hsa_circ_2904,RMVar_hsa_circ_232320,RMVar_hsa_circ_295496,RMVar_hsa_circ_322951,RMVar_hsa_circ_341325,RMVar_hsa_circ_344091,RMVar_hsa_circ_328586,RMVar_hsa_circ_317188,RMVar_hsa_circ_317517,RMVar_hsa_circ_302256,RMVar_hsa_circ_290962,RMVar_hsa_circ_292671,RMVar_hsa_circ_232330,RMVar_hsa_circ_38203,RMVar_hsa_circ_52311,RMVar_hsa_circ_232331,RMVar_hsa_circ_232332,RMVar_hsa_circ_232328,RMVar_hsa_circ_232329,RMVar_hsa_circ_232327,RMVar_hsa_circ_46657,RMVar_hsa_circ_302712,RMVar_hsa_circ_337575,RMVar_hsa_circ_90298,RMVar_hsa_circ_38619,RMVar_hsa_circ_232333 20891 RMVar_ID_20891 Human_SNP_ID_236508653 A-to-I Human chr5 + 72871196 72871196 72871196 GCAGGGTTTCACCATGTTGGCCAGGCTGGTCTAGAACTCCTGACCTCAAGTGATCCGCCCGCCTC GCAGGGTTTCACCATGTTGGCCAGGCTGGTCTGGAACTCCTGACCTCAAGTGATCCGCCCGCCTC A G TNPO1 Ensembl:ENSG00000083312 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs968337271 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2435,RMVar_hsa_circ_67841,RMVar_hsa_circ_232317,RMVar_hsa_circ_113732,RMVar_hsa_circ_232313,RMVar_hsa_circ_318015,RMVar_hsa_circ_71542,RMVar_hsa_circ_232315,RMVar_hsa_circ_44267,RMVar_hsa_circ_87992,RMVar_hsa_circ_94224,RMVar_hsa_circ_232319,RMVar_hsa_circ_77211,RMVar_hsa_circ_232318,RMVar_hsa_circ_275788,RMVar_hsa_circ_311388,RMVar_hsa_circ_334685,RMVar_hsa_circ_344318,RMVar_hsa_circ_321205,RMVar_hsa_circ_295973,RMVar_hsa_circ_52640,RMVar_hsa_circ_26926,RMVar_hsa_circ_45831,RMVar_hsa_circ_59485,RMVar_hsa_circ_28505,RMVar_hsa_circ_232321,RMVar_hsa_circ_2904,RMVar_hsa_circ_232320,RMVar_hsa_circ_295496,RMVar_hsa_circ_322951,RMVar_hsa_circ_341325,RMVar_hsa_circ_344091,RMVar_hsa_circ_328586,RMVar_hsa_circ_317188,RMVar_hsa_circ_317517,RMVar_hsa_circ_302256,RMVar_hsa_circ_290962,RMVar_hsa_circ_292671,RMVar_hsa_circ_232330,RMVar_hsa_circ_38203,RMVar_hsa_circ_52311,RMVar_hsa_circ_232331,RMVar_hsa_circ_232332,RMVar_hsa_circ_232328,RMVar_hsa_circ_232329,RMVar_hsa_circ_232327,RMVar_hsa_circ_46657,RMVar_hsa_circ_302712,RMVar_hsa_circ_337575,RMVar_hsa_circ_90298,RMVar_hsa_circ_38619,RMVar_hsa_circ_232333 20892 RMVar_ID_20892 Human_SNP_ID_236511098 A-to-I Human chr5 + 72880606 72880606 72880606 GGAGTCCAAGGCGGGTGTATCACCTGAGGTCTAGAGTTCAAGACCAGCTTGGCCAACATGGTGAA GGAGTCCAAGGCGGGTGTATCACCTGAGGTCTGGAGTTCAAGACCAGCTTGGCCAACATGGTGAA A G TNPO1 Ensembl:ENSG00000083312 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs990900208 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67841,RMVar_hsa_circ_232317,RMVar_hsa_circ_113732,RMVar_hsa_circ_232315,RMVar_hsa_circ_44267,RMVar_hsa_circ_87992,RMVar_hsa_circ_94224,RMVar_hsa_circ_232319,RMVar_hsa_circ_77211,RMVar_hsa_circ_232318,RMVar_hsa_circ_311388,RMVar_hsa_circ_334685,RMVar_hsa_circ_321205,RMVar_hsa_circ_52640,RMVar_hsa_circ_26926,RMVar_hsa_circ_45831,RMVar_hsa_circ_59485,RMVar_hsa_circ_28505,RMVar_hsa_circ_2904,RMVar_hsa_circ_232320,RMVar_hsa_circ_322951,RMVar_hsa_circ_344091,RMVar_hsa_circ_328586,RMVar_hsa_circ_317188,RMVar_hsa_circ_302256,RMVar_hsa_circ_290962,RMVar_hsa_circ_292671,RMVar_hsa_circ_232330,RMVar_hsa_circ_38203,RMVar_hsa_circ_52311,RMVar_hsa_circ_232331,RMVar_hsa_circ_232332,RMVar_hsa_circ_337575,RMVar_hsa_circ_90298,RMVar_hsa_circ_38619,RMVar_hsa_circ_1962,RMVar_hsa_circ_9237,RMVar_hsa_circ_45793,RMVar_hsa_circ_334991,RMVar_hsa_circ_371614,RMVar_hsa_circ_232333,RMVar_hsa_circ_68544,RMVar_hsa_circ_26354,RMVar_hsa_circ_232334,RMVar_hsa_circ_232336,RMVar_hsa_circ_232335,RMVar_hsa_circ_3265,RMVar_hsa_circ_232338,RMVar_hsa_circ_278669,RMVar_hsa_circ_349123,RMVar_hsa_circ_1315,RMVar_hsa_circ_373169,RMVar_hsa_circ_331271,RMVar_hsa_circ_20771,RMVar_hsa_circ_103424,RMVar_hsa_circ_232339,RMVar_hsa_circ_232340 20893 RMVar_ID_20893 Human_SNP_ID_236513942 A-to-I Human chr5 + 72890885 72890881 72890885 AAAAGGAATTTTTTTGTGTGTGACAAGGTCTCACTCTGTCACCTAGGCTAGAGTGCAGTGGTGTG AAAAGGAATTTTTTTGTGTGTGACAAGGT____CTCTGTCACCTAGGCTAGAGTGCAGTGGTGTG TCTCA T TNPO1 Ensembl:ENSG00000083312 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs937435974 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_67841,RMVar_hsa_circ_44267,RMVar_hsa_circ_87992,RMVar_hsa_circ_232319,RMVar_hsa_circ_77211,RMVar_hsa_circ_232318,RMVar_hsa_circ_334685,RMVar_hsa_circ_26926,RMVar_hsa_circ_59485,RMVar_hsa_circ_28505,RMVar_hsa_circ_322951,RMVar_hsa_circ_344091,RMVar_hsa_circ_328586,RMVar_hsa_circ_317188,RMVar_hsa_circ_290962,RMVar_hsa_circ_38203,RMVar_hsa_circ_232332,RMVar_hsa_circ_38619,RMVar_hsa_circ_14338,RMVar_hsa_circ_24661,RMVar_hsa_circ_1962,RMVar_hsa_circ_26354,RMVar_hsa_circ_232334,RMVar_hsa_circ_3265,RMVar_hsa_circ_349123,RMVar_hsa_circ_20771,RMVar_hsa_circ_103424,RMVar_hsa_circ_232340,RMVar_hsa_circ_47550,RMVar_hsa_circ_107469,RMVar_hsa_circ_232343,RMVar_hsa_circ_104539,RMVar_hsa_circ_326167,RMVar_hsa_circ_374193,RMVar_hsa_circ_304323,RMVar_hsa_circ_120268,RMVar_hsa_circ_115475,RMVar_hsa_circ_232345,RMVar_hsa_circ_232349,RMVar_hsa_circ_85413,RMVar_hsa_circ_232347,RMVar_hsa_circ_232348,RMVar_hsa_circ_232346,RMVar_hsa_circ_84260,RMVar_hsa_circ_308350,RMVar_hsa_circ_232344,RMVar_hsa_circ_50056,RMVar_hsa_circ_127975,RMVar_hsa_circ_305516,RMVar_hsa_circ_232355,RMVar_hsa_circ_232356,RMVar_hsa_circ_321712,RMVar_hsa_circ_359902,RMVar_hsa_circ_310299,RMVar_hsa_circ_296114,RMVar_hsa_circ_304385,RMVar_hsa_circ_273675,RMVar_hsa_circ_232358,RMVar_hsa_circ_232360,RMVar_hsa_circ_46286,RMVar_hsa_circ_232359,RMVar_hsa_circ_232357 20894 RMVar_ID_20894 Human_SNP_ID_236517784 A-to-I Human chr5 + 72905736 72905736 72905736 GGCCAACATGGTGAAAACCCATCTCTACTAAAAATACAAAAATTAGCCACGTGTGGTGGGACGTG GGCCAACATGGTGAAAACCCATCTCTACTAAAGATACAAAAATTAGCCACGTGTGGTGGGACGTG A G TNPO1 Ensembl:ENSG00000083312 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs530734596 Functional Loss SNV dbSNP153 33..33 33 - - - 20895 RMVar_ID_20895 Human_SNP_ID_236518050 A-to-I Human chr5 + 72906457 72906457 72906457 GGCATTACAGGCACATGCCACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCA GGCATTACAGGCACATGCCACCATGCCTGGCTGATTTTTGTATTTTTAGTAGAGATGGGGTTTCA A G TNPO1 Ensembl:ENSG00000083312 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1157634286 Functional Loss SNV dbSNP153 33..33 33 - - - 20896 RMVar_ID_20896 Human_SNP_ID_236518060 A-to-I Human chr5 + 72906492 72906492 72906492 TTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCGGGCTGGTCTCGAACTCCTGACCT TTTTGTATTTTTAGTAGAGATGGGGTTTCACCGTGTTGGCCGGGCTGGTCTCGAACTCCTGACCT A G TNPO1 Ensembl:ENSG00000083312 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1336828802 Functional Loss SNV dbSNP153 33..33 33 - - - 20897 RMVar_ID_20897 Human_SNP_ID_236520750 A-to-I Human chr5 + 72916178 72916178 72916178 TTTTTTTAGGAGAGAGTTTGGCCGTGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCGAGTGAAC TTTTTTTAGGAGAGAGTTTGGCCGTGTTGGCCGGGCTGGTCTCGAACTCCTGACCTCGAGTGAAC A G TNPO1 Ensembl:ENSG00000083312 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs555629540 Functional Loss SNV dbSNP153 33..33 33 - - - 20898 RMVar_ID_20898 Human_SNP_ID_236533451 A-to-I Human chr5 + 72967179 72967178 72967180 GTGGTGGTGCACACCTGTAATCCCAGCTACTCAGGGGGCTGAAGCACAAGAATCGCTTGAACCCG GTGGTGGTGCACACCTGTAATCCCAGCTACTC__GGGGCTGAAGCACAAGAATCGCTTGAACCCG CAG C FCHO2 Ensembl:ENSG00000157107 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1393831677 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_104922,RMVar_hsa_circ_121507,RMVar_hsa_circ_232368,RMVar_hsa_circ_232369 20899 RMVar_ID_20899 Human_SNP_ID_236553082 A-to-I Human chr5 + 73048342 73048342 73048342 TGTGGTGGTAGGCGCCTGTAATCCCAGCTGTTAGGGAGGCTGAGGAAGGAGAATCACTGCAGGAG TGTGGTGGTAGGCGCCTGTAATCCCAGCTGTTGGGGAGGCTGAGGAAGGAGAATCACTGCAGGAG A G FCHO2 Ensembl:ENSG00000157107 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1000731926 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17575415 RMVar_hsa_circ_104922,RMVar_hsa_circ_232369,RMVar_hsa_circ_67310,RMVar_hsa_circ_58180,RMVar_hsa_circ_103638,RMVar_hsa_circ_112211,RMVar_hsa_circ_93219,RMVar_hsa_circ_67787,RMVar_hsa_circ_232373,RMVar_hsa_circ_232374,RMVar_hsa_circ_316882,RMVar_hsa_circ_350709,RMVar_hsa_circ_70442,RMVar_hsa_circ_84321,RMVar_hsa_circ_57035,RMVar_hsa_circ_115651,RMVar_hsa_circ_232381,RMVar_hsa_circ_232382,RMVar_hsa_circ_232380,RMVar_hsa_circ_335178,RMVar_hsa_circ_232386,RMVar_hsa_circ_232388,RMVar_hsa_circ_18719,RMVar_hsa_circ_232387,RMVar_hsa_circ_346310,RMVar_hsa_circ_321944,RMVar_hsa_circ_100015,RMVar_hsa_circ_232390 20900 RMVar_ID_20900 Human_SNP_ID_236675617 A-to-I Human chr5 - 73560585 73560585 73560585 GCTCAGGAATTCGAGACTGGCCAGGGCAACATAGCAAGACCCTGTCTCTACTAAAAATGCAAAAA GCTCAGGAATTCGAGACTGGCCAGGGCAACATTGCAAGACCCTGTCTCTACTAAAAATGCAAAAA T A ANKRA2 Ensembl:ENSG00000164331 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1368301754 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75111,RMVar_hsa_circ_330410,RMVar_hsa_circ_232429,RMVar_hsa_circ_282855,RMVar_hsa_circ_232430,RMVar_hsa_circ_351996,RMVar_hsa_circ_232431,RMVar_hsa_circ_306958 20901 RMVar_ID_20901 Human_SNP_ID_236962922 A-to-I Human chr5 - 74745223 74745223 74745223 CTCCTGCCTCAGCCTCCTGGGTAGCTGGGATTACAGGCACGCACCACCACTCCAAGCTAATTTTT CTCCTGCCTCAGCCTCCTGGGTAGCTGGGATTCCAGGCACGCACCACCACTCCAAGCTAATTTTT T G GFM2 Ensembl:ENSG00000164347 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1478604479 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74317,RMVar_hsa_circ_46039,RMVar_hsa_circ_101228,RMVar_hsa_circ_232484,RMVar_hsa_circ_232485,RMVar_hsa_circ_350928,RMVar_hsa_circ_359874,RMVar_hsa_circ_60456,RMVar_hsa_circ_374071,RMVar_hsa_circ_101580,RMVar_hsa_circ_232486,RMVar_hsa_circ_44409,RMVar_hsa_circ_34418,RMVar_hsa_circ_232487 20902 RMVar_ID_20902 Human_SNP_ID_236969871 A-to-I Human chr5 + 74772333 74772333 74772333 ATTTTTTTGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGGTCTCGATCTCCGTGATCCGCCC ATTTTTTTGTAGAGACGGGGTTTCACCGTGTTGGCCAGGATGGTCTCGATCTCCGTGATCCGCCC A G NSA2 Ensembl:ENSG00000164346 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1249312961 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95483,RMVar_hsa_circ_232492 20903 RMVar_ID_20903 Human_SNP_ID_236976891 A-to-I Human chr5 - 74799412 74799412 74799412 GCCAATCCAAGCTGAGGACTGTGGAGCGAATCAGCTTTTTAATGTGCTTGCTCACCCACCAGTCA GCCAATCCAAGCTGAGGACTGTGGAGCGAATCGGCTTTTTAATGTGCTTGCTCACCCACCAGTCA T C FAM169A Ensembl:ENSG00000198780 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1314100822 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_232496,RMVar_hsa_circ_268788,RMVar_hsa_circ_232493,RMVar_hsa_circ_232498,RMVar_hsa_circ_273983,RMVar_hsa_circ_310899,RMVar_hsa_circ_290453,RMVar_hsa_circ_271348,RMVar_hsa_circ_232497,RMVar_hsa_circ_232495 20904 RMVar_ID_20904 Human_SNP_ID_236992096 A-to-I Human chr5 - 74861323 74861323 74861323 AGATAATAGAGATTTGGGAGCTACCAGTGTATATATTTGGTAAATGGAGCCAGTAGACAGGGTAA AGATAATAGAGATTTGGGAGCTACCAGTGTATGTATTTGGTAAATGGAGCCAGTAGACAGGGTAA T C FAM169A Ensembl:ENSG00000198780 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559977905 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124615,RMVar_hsa_circ_232506,RMVar_hsa_circ_122727,RMVar_hsa_circ_232507 20905 RMVar_ID_20905 Human_SNP_ID_236992102 A-to-I Human chr5 - 74861337 74861337 74861337 TCAAAGATCTAGGCAGATAATAGAGATTTGGGAGCTACCAGTGTATATATTTGGTAAATGGAGCC TCAAAGATCTAGGCAGATAATAGAGATTTGGGTGCTACCAGTGTATATATTTGGTAAATGGAGCC T A FAM169A Ensembl:ENSG00000198780 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1032061032 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124615,RMVar_hsa_circ_232506,RMVar_hsa_circ_122727,RMVar_hsa_circ_232507 20906 RMVar_ID_20906 Human_SNP_ID_236992106 A-to-I Human chr5 - 74861350 74861350 74861350 TTGCAAATATGAATCAAAGATCTAGGCAGATAATAGAGATTTGGGAGCTACCAGTGTATATATTT TTGCAAATATGAATCAAAGATCTAGGCAGATAGTAGAGATTTGGGAGCTACCAGTGTATATATTT T C FAM169A Ensembl:ENSG00000198780 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1172621269 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124615,RMVar_hsa_circ_232506,RMVar_hsa_circ_122727,RMVar_hsa_circ_232507 20907 RMVar_ID_20907 Human_SNP_ID_236992107 A-to-I Human chr5 - 74861351 74861351 74861351 GTTGCAAATATGAATCAAAGATCTAGGCAGATAATAGAGATTTGGGAGCTACCAGTGTATATATT GTTGCAAATATGAATCAAAGATCTAGGCAGATTATAGAGATTTGGGAGCTACCAGTGTATATATT T A FAM169A Ensembl:ENSG00000198780 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054537745 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124615,RMVar_hsa_circ_232506,RMVar_hsa_circ_122727,RMVar_hsa_circ_232507 20908 RMVar_ID_20908 Human_SNP_ID_193991231 A-to-I Human chr4 + 91450508 91450508 91450508 ACAGGTTTCACACATCGGACTATAGGTGTCACAGTATAGTAATCTTGGAGTGAGGAGAAACAAAC ACAGGTTTCACACATCGGACTATAGGTGTCACTGTATAGTAATCTTGGAGTGAGGAGAAACAAAC A T CCSER1 Ensembl:ENSG00000184305 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1432502114 Functional Loss SNV dbSNP153 33..33 33 - - - 20909 RMVar_ID_20909 Human_SNP_ID_194241937 A-to-I Human chr4 + 92401921 92401921 92401921 TATGCAATGCTGCTTGAAAGCATTTTACCCACAGTAGAATTTCTTTCAAAATTGGAGTTTATTCT TATGCAATGCTGCTTGAAAGCATTTTACCCACGGTAGAATTTCTTTCAAAATTGGAGTTTATTCT A G GRID2 Ensembl:ENSG00000152208 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1237777350 Functional Loss SNV dbSNP153 33..33 33 - - - 20910 RMVar_ID_20910 Human_SNP_ID_194327353 A-to-I Human chr4 + 92718656 92718656 92718656 ATGATGTTGCATGCCTGTAGCCATAGATGATCAGGAGGCTCAGGCAGGAAGATTGCTTGAACCCA ATGATGTTGCATGCCTGTAGCCATAGATGATCTGGAGGCTCAGGCAGGAAGATTGCTTGAACCCA A T GRID2 Ensembl:ENSG00000152208 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs974235854 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9892 20911 RMVar_ID_20911 Human_SNP_ID_194327542 A-to-I Human chr4 + 92719261 92719261 92719261 CACTCGCCTCAGTCTCCCAAAGTGCTGGGATTACAGGCATGAGTCACTGTGCCTGGCCAAAAGAC CACTCGCCTCAGTCTCCCAAAGTGCTGGGATTTCAGGCATGAGTCACTGTGCCTGGCCAAAAGAC A T GRID2 Ensembl:ENSG00000152208 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1425359985 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9892 20912 RMVar_ID_20912 Human_SNP_ID_194331535 A-to-I Human chr4 + 92734493 92734493 92734493 TTTTATAAAGATAGGTTCTTGCTATGTTGCCCAAGTTGGTCTTGAACTCTTGGCCTCAAGTGACC TTTTATAAAGATAGGTTCTTGCTATGTTGCCCCAGTTGGTCTTGAACTCTTGGCCTCAAGTGACC A C GRID2 Ensembl:ENSG00000152208 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1036772406 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9892 20913 RMVar_ID_20913 Human_SNP_ID_194332713 A-to-I Human chr4 + 92738785 92738785 92738785 GTGATTCTCCTACCTCAGCCTCCTCAGTAGCTAAGACTAATGGCATGCACCACCATGTCAGCTAA GTGATTCTCCTACCTCAGCCTCCTCAGTAGCTGAGACTAATGGCATGCACCACCATGTCAGCTAA A G GRID2 Ensembl:ENSG00000152208 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1021174506 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9892 20914 RMVar_ID_20914 Human_SNP_ID_194353830 A-to-I Human chr4 + 92817753 92817753 92817753 TGGTGTCTCACTATATTGCCCATGCTAGTCTCAAACTCCTTGGCCCAAGTGATCCTCTCCCTTGG TGGTGTCTCACTATATTGCCCATGCTAGTCTCTAACTCCTTGGCCCAAGTGATCCTCTCCCTTGG A T GRID2 Ensembl:ENSG00000152208 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1560610477 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9892 20915 RMVar_ID_20915 Human_SNP_ID_194353834 A-to-I Human chr4 + 92817767 92817767 92817767 ATTGCCCATGCTAGTCTCAAACTCCTTGGCCCAAGTGATCCTCTCCCTTGGCCTCTCAAAGTGTT ATTGCCCATGCTAGTCTCAAACTCCTTGGCCCCAGTGATCCTCTCCCTTGGCCTCTCAAAGTGTT A C GRID2 Ensembl:ENSG00000152208 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs946385697 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9892 20916 RMVar_ID_20916 Human_SNP_ID_194374222 A-to-I Human chr4 + 92896786 92896786 92896786 TGTGTGTGAGACGGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCGATCTTTGCTCAC TGTGTGTGAGACGGAGTCTCGCTCTGTCGCCCGGGCTGGAGTGCAGTGGCGCGATCTTTGCTCAC A G GRID2 Ensembl:ENSG00000152208 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1445362638 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9892 20917 RMVar_ID_20917 Human_SNP_ID_194375256 A-to-I Human chr4 + 92900736 92900736 92900736 TGTGCCTGTAGTCCCAGCTACGCCGGAGGCTGAGGCAGGAGAATGGCATGAACCTGGGAGGCGGA TGTGCCTGTAGTCCCAGCTACGCCGGAGGCTGCGGCAGGAGAATGGCATGAACCTGGGAGGCGGA A C GRID2 Ensembl:ENSG00000152208 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1474927261 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9892 20918 RMVar_ID_20918 Human_SNP_ID_194377215 A-to-I Human chr4 + 92907585 92907585 92907585 AGGCATGTGCCACCACACCTGGCTAATTTTGTATTTTTAGTAGAGATGGGTTTCTCCATGCTTGT AGGCATGTGCCACCACACCTGGCTAATTTTGTGTTTTTAGTAGAGATGGGTTTCTCCATGCTTGT A G GRID2 Ensembl:ENSG00000152208 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1251791469 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9892 20919 RMVar_ID_20919 Human_SNP_ID_194377307 A-to-I Human chr4 + 92907867 92907867 92907867 CCAACATGGTGAATCCCTGTCTCTACAAAAACACAAAAATTAGCTGGATGTGTTAGGGTGCGCTT CCAACATGGTGAATCCCTGTCTCTACAAAAACGCAAAAATTAGCTGGATGTGTTAGGGTGCGCTT A G GRID2 Ensembl:ENSG00000152208 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1296189360 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9892 20920 RMVar_ID_20920 Human_SNP_ID_194394838 A-to-I Human chr4 + 92959920 92959920 92959920 GAGAAATACCTAATGTAGATGATGGGTTGATGAGTGCATCAAACCACCATGGCACATGTGTACCT GAGAAATACCTAATGTAGATGATGGGTTGATGGGTGCATCAAACCACCATGGCACATGTGTACCT A G GRID2 Ensembl:ENSG00000152208 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs954130759 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9892 20921 RMVar_ID_20921 Human_SNP_ID_194727131 A-to-I Human chr4 + 94284430 94284429 94284431 GTAGTTGTAATGTTTTGTTTTGTTTTTGAGACAGAGCCTCACTCTGGCTGGAGTGCAGTGGCACC GTAGTTGTAATGTTTTGTTTTGTTTTTGAGAC__AGCCTCACTCTGGCTGGAGTGCAGTGGCACC CAG C SMARCAD1 Ensembl:ENSG00000163104 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1409615882 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_51750,RMVar_hsa_circ_312769,RMVar_hsa_circ_227529,RMVar_hsa_circ_56326,RMVar_hsa_circ_270219,RMVar_hsa_circ_227538,RMVar_hsa_circ_227539,RMVar_hsa_circ_227541,RMVar_hsa_circ_16225,RMVar_hsa_circ_373065,RMVar_hsa_circ_34616,RMVar_hsa_circ_227542,RMVar_hsa_circ_343354,RMVar_hsa_circ_292695 20922 RMVar_ID_20922 Human_SNP_ID_194727155 A-to-I Human chr4 + 94284492 94284492 94284492 ACCATCTCTGCTCACTTCAATCTCCACCTCCCAGGTTCAAGCAATTCCCATGCCTTAGCCTCCCA ACCATCTCTGCTCACTTCAATCTCCACCTCCCGGGTTCAAGCAATTCCCATGCCTTAGCCTCCCA A G SMARCAD1 Ensembl:ENSG00000163104 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1204006034 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51750,RMVar_hsa_circ_312769,RMVar_hsa_circ_227529,RMVar_hsa_circ_56326,RMVar_hsa_circ_270219,RMVar_hsa_circ_227538,RMVar_hsa_circ_227539,RMVar_hsa_circ_227541,RMVar_hsa_circ_16225,RMVar_hsa_circ_373065,RMVar_hsa_circ_34616,RMVar_hsa_circ_227542,RMVar_hsa_circ_343354,RMVar_hsa_circ_292695 20923 RMVar_ID_20923 Human_SNP_ID_194810176 A-to-I Human chr4 + 94624195 94624195 94624195 AAGAAGTTGGCTGGGCATGGTGGTGCACGCCTATGGTCCCAGCTGCTCGGGAGGCTGAGATGGGA AAGAAGTTGGCTGGGCATGGTGGTGCACGCCTGTGGTCCCAGCTGCTCGGGAGGCTGAGATGGGA A G PDLIM5 Ensembl:ENSG00000163110 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946650583 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89208,RMVar_hsa_circ_335978,RMVar_hsa_circ_357757,RMVar_hsa_circ_278855,RMVar_hsa_circ_61986,RMVar_hsa_circ_227550,RMVar_hsa_circ_303405,RMVar_hsa_circ_227553,RMVar_hsa_circ_337835,RMVar_hsa_circ_367515,RMVar_hsa_circ_329905,RMVar_hsa_circ_10396,RMVar_hsa_circ_120875,RMVar_hsa_circ_332905,RMVar_hsa_circ_227554,RMVar_hsa_circ_338070,RMVar_hsa_circ_227557,RMVar_hsa_circ_33914,RMVar_hsa_circ_227556,RMVar_hsa_circ_34938,RMVar_hsa_circ_279391,RMVar_hsa_circ_317304,RMVar_hsa_circ_66335,RMVar_hsa_circ_227561 20924 RMVar_ID_20924 Human_SNP_ID_194811372 A-to-I Human chr4 + 94629073 94629073 94629073 TGATATTAAGATGATTTAGAAGATTCTGGGCCAGGCACAGTGGCCCATGCCTGTAATCCCAGCAC TGATATTAAGATGATTTAGAAGATTCTGGGCCTGGCACAGTGGCCCATGCCTGTAATCCCAGCAC A T PDLIM5 Ensembl:ENSG00000163110 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs546563514 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89208,RMVar_hsa_circ_335978,RMVar_hsa_circ_357757,RMVar_hsa_circ_278855,RMVar_hsa_circ_61986,RMVar_hsa_circ_227550,RMVar_hsa_circ_303405,RMVar_hsa_circ_227553,RMVar_hsa_circ_337835,RMVar_hsa_circ_367515,RMVar_hsa_circ_329905,RMVar_hsa_circ_10396,RMVar_hsa_circ_120875,RMVar_hsa_circ_332905,RMVar_hsa_circ_227554,RMVar_hsa_circ_338070,RMVar_hsa_circ_227557,RMVar_hsa_circ_33914,RMVar_hsa_circ_227556,RMVar_hsa_circ_34938,RMVar_hsa_circ_279391,RMVar_hsa_circ_317304,RMVar_hsa_circ_66335,RMVar_hsa_circ_227561 20925 RMVar_ID_20925 Human_SNP_ID_194818621 A-to-I Human chr4 + 94660886 94660886 94660886 CATAAAAGAAAATTAGGTCAACCAGCCTGGGCAAGATGGGGAAACCCTGTCTTTACTAAAAATAA CATAAAAGAAAATTAGGTCAACCAGCCTGGGCGAGATGGGGAAACCCTGTCTTTACTAAAAATAA A G PDLIM5 Ensembl:ENSG00000163110 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1266150541 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61986,RMVar_hsa_circ_303405,RMVar_hsa_circ_120875,RMVar_hsa_circ_338070,RMVar_hsa_circ_227557,RMVar_hsa_circ_227556,RMVar_hsa_circ_317304,RMVar_hsa_circ_301218,RMVar_hsa_circ_83900,RMVar_hsa_circ_227564 20926 RMVar_ID_20926 Human_SNP_ID_195040644 A-to-I Human chr4 - 95548088 95548088 95548088 CAGGCCCGGGATGTGCATGCCTCTGCACTCATACATACCCCGCTTCATGCCTGCTTCCCACCAGG CAGGCCCGGGATGTGCATGCCTCTGCACTCATTCATACCCCGCTTCATGCCTGCTTCCCACCAGG T A UNC5C Ensembl:ENSG00000182168 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1423894480 Functional Loss SNV dbSNP153 33..33 33 - - - 20927 RMVar_ID_20927 Human_SNP_ID_195040645 A-to-I Human chr4 - 95548088 95548088 95548088 CAGGCCCGGGATGTGCATGCCTCTGCACTCATACATACCCCGCTTCATGCCTGCTTCCCACCAGG CAGGCCCGGGATGTGCATGCCTCTGCACTCATGCATACCCCGCTTCATGCCTGCTTCCCACCAGG T C UNC5C Ensembl:ENSG00000182168 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1423894480 Functional Loss SNV dbSNP153 33..33 33 - - - 20928 RMVar_ID_20928 Human_SNP_ID_195119004 A-to-I Human chr4 - 95841032 95841032 95841032 ATTTCTTCTCGTGTACGATAACTGACTCCAGGATCACTCATACTGTGTCCATGATAACGGTAGGT ATTTCTTCTCGTGTACGATAACTGACTCCAGGGTCACTCATACTGTGTCCATGATAACGGTAGGT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1420995483 Functional Loss SNV dbSNP153 33..33 33 - - - 20929 RMVar_ID_20929 Human_SNP_ID_195119013 A-to-I Human chr4 - 95841047 95841047 95841047 CTTCTTACTTCCTGAATTTCTTCTCGTGTACGATAACTGACTCCAGGATCACTCATACTGTGTCC CTTCTTACTTCCTGAATTTCTTCTCGTGTACGGTAACTGACTCCAGGATCACTCATACTGTGTCC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1370609503 Functional Loss SNV dbSNP153 33..33 33 - - - 20930 RMVar_ID_20930 Human_SNP_ID_195386955 A-to-I Human chr4 + 96902887 96902887 96902887 GCTTCCCACAGGCATTTTAAAAATAAAGTTCCAGAGAAACAAAAACTGTTCCAGGAGGATGATGG GCTTCCCACAGGCATTTTAAAAATAAAGTTCCGGAGAAACAAAAACTGTTCCAGGAGGATGATGG A G COX7A2P2 Ensembl:ENSG00000236764 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879206966 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8596607 20931 RMVar_ID_20931 Human_SNP_ID_195386959 A-to-I Human chr4 + 96902896 96902896 96902896 AGGCATTTTAAAAATAAAGTTCCAGAGAAACAAAAACTGTTCCAGGAGGATGATGGAATTCCACT AGGCATTTTAAAAATAAAGTTCCAGAGAAACAGAAACTGTTCCAGGAGGATGATGGAATTCCACT A G COX7A2P2 Ensembl:ENSG00000236764 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1352495961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1140021,Human_RBP_ID_4801324,Human_RBP_ID_8596607,Human_RBP_ID_17667899,Human_RBP_ID_27731314 20932 RMVar_ID_20932 Human_SNP_ID_195737640 A-to-I Human chr4 + 98293402 98293402 98293402 TAAGGTTGAGTTTCTGATTTTTTTTTTTCTTTAAGCAGATAATCTCAGTGATACCTTGAAGAAGC TAAGGTTGAGTTTCTGATTTTTTTTTTTCTTTTAGCAGATAATCTCAGTGATACCTTGAAGAAGC A T RAP1GDS1 Ensembl:ENSG00000138698 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1285394442 Functional Loss SNV dbSNP153 33..33 33 - - - 20933 RMVar_ID_20933 Human_SNP_ID_195756602 A-to-I Human chr4 + 98368280 98368280 98368280 TGATTGTGAGGCTTCCCCTGCCATGCGGAACTATAAGACCAATTAAACCTCTTCCTTTTGTAAAT TGATTGTGAGGCTTCCCCTGCCATGCGGAACTGTAAGACCAATTAAACCTCTTCCTTTTGTAAAT A G RAP1GDS1 Ensembl:ENSG00000138698 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1248608318 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2867744 RMVar_hsa_circ_60116,RMVar_hsa_circ_24846,RMVar_hsa_circ_318061,RMVar_hsa_circ_45922,RMVar_hsa_circ_117721,RMVar_hsa_circ_227608,RMVar_hsa_circ_311934,RMVar_hsa_circ_343817,RMVar_hsa_circ_97478,RMVar_hsa_circ_48087,RMVar_hsa_circ_227609 20934 RMVar_ID_20934 Human_SNP_ID_195807228 A-to-I Human chr4 - 98585447 98585447 98585447 AAAATGGCCAGGTGTGGCGGTGCATGCCTGTAATCCTAGCTACTTGGGAGGCTGAGGCAGGAGAA AAAATGGCCAGGTGTGGCGGTGCATGCCTGTATTCCTAGCTACTTGGGAGGCTGAGGCAGGAGAA T A TSPAN5 Ensembl:ENSG00000168785 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1185384536 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121310,RMVar_hsa_circ_227622 20935 RMVar_ID_20935 Human_SNP_ID_195815388 A-to-I Human chr4 - 98621571 98621571 98621571 GAGGTCAGGAGATCGAGAGCATCCTGGTGAACATGGTGAAACCCCGTCTCTACTAAAAATACAAA GAGGTCAGGAGATCGAGAGCATCCTGGTGAACGTGGTGAAACCCCGTCTCTACTAAAAATACAAA T C TSPAN5 Ensembl:ENSG00000168785 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1335773775 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121310,RMVar_hsa_circ_227622 20936 RMVar_ID_20936 Human_SNP_ID_195876109 A-to-I Human chr4 - 98883682 98883682 98883682 AGTAATATTTGACACCAGGCGCAGTGGCTCACACCTGTAATCGCAGCACTTTGGGAGGCTGAGGC AGTAATATTTGACACCAGGCGCAGTGGCTCACGCCTGTAATCGCAGCACTTTGGGAGGCTGAGGC T C EIF4E Ensembl:ENSG00000151247 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs757209380 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17575159 RMVar_hsa_circ_227627,RMVar_hsa_circ_93817 20937 RMVar_ID_20937 Human_SNP_ID_195876607 A-to-I Human chr4 - 98885615 98885615 98885615 AAACCCTGTCTCTACAAAAAATACAAAAATTAACTGGGTATGGTGACATGTCCCTGTATGTATGC AAACCCTGTCTCTACAAAAAATACAAAAATTAGCTGGGTATGGTGACATGTCCCTGTATGTATGC T C EIF4E Ensembl:ENSG00000151247 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1279426608 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_227627,RMVar_hsa_circ_93817,RMVar_hsa_circ_39129 20938 RMVar_ID_20938 Human_SNP_ID_195876717 A-to-I Human chr4 - 98886116 98886116 98886116 TAGAGACAGGGTCTTGTTCTGTCGCCCAGGCTAGAGTGCAGTGGGGCCATCATAGCTCACTGTAG TAGAGACAGGGTCTTGTTCTGTCGCCCAGGCTGGAGTGCAGTGGGGCCATCATAGCTCACTGTAG T C EIF4E Ensembl:ENSG00000151247 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1043155043 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_227627,RMVar_hsa_circ_93817,RMVar_hsa_circ_39129 20939 RMVar_ID_20939 Human_SNP_ID_195876724 A-to-I Human chr4 - 98886147 98886147 98886147 TGTTTGAATAAGTGACTATTTTGCTTTTTTTTAGAGACAGGGTCTTGTTCTGTCGCCCAGGCTAG TGTTTGAATAAGTGACTATTTTGCTTTTTTTTTGAGACAGGGTCTTGTTCTGTCGCCCAGGCTAG T A EIF4E Ensembl:ENSG00000151247 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs895672925 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_227627,RMVar_hsa_circ_93817,RMVar_hsa_circ_39129 20940 RMVar_ID_20940 Human_SNP_ID_195883219 A-to-I Human chr4 - 98912087 98912087 98912087 CCACCATGCCCAGCTAATTTTGTGTTTTTGGTAGAGATGGGGTTTCACCATGTTAGTCATGTGGG CCACCATGCCCAGCTAATTTTGTGTTTTTGGTGGAGATGGGGTTTCACCATGTTAGTCATGTGGG T C EIF4E Ensembl:ENSG00000151247 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1416102117 Functional Loss SNV dbSNP153 33..33 33 - - - 20941 RMVar_ID_20941 Human_SNP_ID_195883345 A-to-I Human chr4 - 98912524 98912524 98912525 TTCGCTATGCTGGAGTGCAGTGGTGCGATCTCAGCTCACTGCAATCTCTGATTCCCTGGTTCAAG TTCGCTATGCTGGAGTGCAGTGGTGCGATCTTGGCTCACTGCAATCTCTGATTCCCTGGTTCAAG TG CA EIF4E Ensembl:ENSG00000151247 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs34830689 Functional Loss MNV dbSNP153 32..33 33 - - - 20942 RMVar_ID_20942 Human_SNP_ID_195883346 A-to-I Human chr4 - 98912524 98912524 98912524 TTCGCTATGCTGGAGTGCAGTGGTGCGATCTCAGCTCACTGCAATCTCTGATTCCCTGGTTCAAG TTCGCTATGCTGGAGTGCAGTGGTGCGATCTCTGCTCACTGCAATCTCTGATTCCCTGGTTCAAG T A EIF4E Ensembl:ENSG00000151247 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7678710 Functional Loss SNV dbSNP153 33..33 33 - - - 20943 RMVar_ID_20943 Human_SNP_ID_195883347 A-to-I Human chr4 - 98912524 98912524 98912524 TTCGCTATGCTGGAGTGCAGTGGTGCGATCTCAGCTCACTGCAATCTCTGATTCCCTGGTTCAAG TTCGCTATGCTGGAGTGCAGTGGTGCGATCTCGGCTCACTGCAATCTCTGATTCCCTGGTTCAAG T C EIF4E Ensembl:ENSG00000151247 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7678710 Functional Loss SNV dbSNP153 33..33 33 - - - 20944 RMVar_ID_20944 Human_SNP_ID_195883976 A-to-I Human chr4 - 98915072 98915072 98915072 GGGTGTGGTGGCATGTGCCTGTAGTCCCAGCTACTCAGAAGGCTGAGGCGGGAGGATTGATTGAG GGGTGTGGTGGCATGTGCCTGTAGTCCCAGCTGCTCAGAAGGCTGAGGCGGGAGGATTGATTGAG T C EIF4E Ensembl:ENSG00000151247 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs569494807 Functional Loss SNV dbSNP153 33..33 33 - - - 20945 RMVar_ID_20945 Human_SNP_ID_195883977 A-to-I Human chr4 - 98915076 98915076 98915076 AGCTGGGTGTGGTGGCATGTGCCTGTAGTCCCAGCTACTCAGAAGGCTGAGGCGGGAGGATTGAT AGCTGGGTGTGGTGGCATGTGCCTGTAGTCCCTGCTACTCAGAAGGCTGAGGCGGGAGGATTGAT T A EIF4E Ensembl:ENSG00000151247 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1231427119 Functional Loss SNV dbSNP153 33..33 33 - - - 20946 RMVar_ID_20946 Human_SNP_ID_195884899 A-to-I Human chr4 - 98918281 98918281 98918281 TCGGCTCACTGCAACCTCCGCCTCTTGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCGACCAGC TCGGCTCACTGCAACCTCCGCCTCTTGGGTTCGAGCAATTCTCCTGCCTCAGCCTCCCGACCAGC T C EIF4E Ensembl:ENSG00000151247 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1475465643 Functional Loss SNV dbSNP153 33..33 33 - - - 20947 RMVar_ID_20947 Human_SNP_ID_195886630 A-to-I Human chr4 - 98924775 98924775 98924775 CAGCCTGGCCAAAATGGTGAAACCCTGTCTCTACTAAAAATACAAAAATTAGCCAGGCCTGGTGG CAGCCTGGCCAAAATGGTGAAACCCTGTCTCTGCTAAAAATACAAAAATTAGCCAGGCCTGGTGG T C EIF4E Ensembl:ENSG00000151247 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1043595604 Functional Loss SNV dbSNP153 33..33 33 - - - 20948 RMVar_ID_20948 Human_SNP_ID_195886955 A-to-I Human chr4 - 98926083 98926083 98926083 TAGCTCACTGCAGCCTCAAACTCCTGGGCTCAAGAGATGCTTCCATCTCAGCCTCTGGTGTAGCA TAGCTCACTGCAGCCTCAAACTCCTGGGCTCAGGAGATGCTTCCATCTCAGCCTCTGGTGTAGCA T C EIF4E Ensembl:ENSG00000151247 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs943649022 Functional Loss SNV dbSNP153 33..33 33 - - - 20949 RMVar_ID_20949 Human_SNP_ID_195921426 A-to-I Human chr4 - 99069534 99069534 99069534 GGGAGGTCGAGGCTGCTTTGAGCTGTGATTGCACTACCGCACTCCAGCCTGGGTGGCAGAGTGAA GGGAGGTCGAGGCTGCTTTGAGCTGTGATTGCGCTACCGCACTCCAGCCTGGGTGGCAGAGTGAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1046225312 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25828871 20950 RMVar_ID_20950 Human_SNP_ID_195923333 A-to-I Human chr4 - 99077266 99077266 99077266 CTCCTGTCTCAACTTTCCAAAGTACTGGGATTATAGGAGTGAGCCACTGCACCTGGCCCACCGTT CTCCTGTCTCAACTTTCCAAAGTACTGGGATTCTAGGAGTGAGCCACTGCACCTGGCCCACCGTT T G ADH5 Ensembl:ENSG00000197894 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1380386254 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22427,RMVar_hsa_circ_35008,RMVar_hsa_circ_109138,RMVar_hsa_circ_227641 20951 RMVar_ID_20951 Human_SNP_ID_195923336 A-to-I Human chr4 - 99077279 99077279 99077279 GCTCCAAGTTGTCCTCCTGTCTCAACTTTCCAAAGTACTGGGATTATAGGAGTGAGCCACTGCAC GCTCCAAGTTGTCCTCCTGTCTCAACTTTCCACAGTACTGGGATTATAGGAGTGAGCCACTGCAC T G ADH5 Ensembl:ENSG00000197894 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1487459288 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22427,RMVar_hsa_circ_35008,RMVar_hsa_circ_109138,RMVar_hsa_circ_227641 20952 RMVar_ID_20952 Human_SNP_ID_195924676 A-to-I Human chr4 - 99082951 99082951 99082951 TAAGTTACGGCTGGGCATGGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCCAAGGCAGGC TAAGTTACGGCTGGGCATGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGC T C ADH5 Ensembl:ENSG00000197894 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1347200757 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35008,RMVar_hsa_circ_109138,RMVar_hsa_circ_227641,RMVar_hsa_circ_78482,RMVar_hsa_circ_227643 20953 RMVar_ID_20953 Human_SNP_ID_195924767 A-to-I Human chr4 - 99083365 99083365 99083365 CAACTACTGACCTCAAGTGATCCACACGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG CAACTACTGACCTCAAGTGATCCACACGCCTCCGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG T G ADH5 Ensembl:ENSG00000197894 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1022471941 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35008,RMVar_hsa_circ_109138,RMVar_hsa_circ_227641,RMVar_hsa_circ_78482,RMVar_hsa_circ_227643 20954 RMVar_ID_20954 Human_SNP_ID_196044350 A-to-I Human chr4 - 99562005 99562005 99562005 TACCACGCCTGGCTAATTTTTGTATTTTTAGTAGAGACGAGGTATCGCCATGTTGGTCTTGAACT TACCACGCCTGGCTAATTTTTGTATTTTTAGTGGAGACGAGGTATCGCCATGTTGGTCTTGAACT T C TRMT10A Ensembl:ENSG00000145331 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs868205682 Functional Loss SNV dbSNP153 33..33 33 - - - 20955 RMVar_ID_20955 Human_SNP_ID_196044376 A-to-I Human chr4 - 99562088 99562088 99562088 TGGCACACTGCAACCTCTGCCTCCCGGGTTCAAGCGATTCTTCTGCCTCAGCCTCCCGAGTAGCT TGGCACACTGCAACCTCTGCCTCCCGGGTTCAGGCGATTCTTCTGCCTCAGCCTCCCGAGTAGCT T C TRMT10A Ensembl:ENSG00000145331 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285862722 Functional Loss SNV dbSNP153 33..33 33 - - - 20956 RMVar_ID_20956 Human_SNP_ID_196119565 A-to-I Human chr4 - 99880590 99880587 99880591 TTTTTCTTTCTTTCTTTTTTTTTTTAAGAGACAGAGTCTTGCTGTGTTGCCCAGTCTGGAGTGCA TTTTTCTTTCTTTCTTTTTTTTTTTAAGAGA____GTCTTGCTGTGTTGCCCAGTCTGGAGTGCA CTCTG C LAMTOR3 Ensembl:ENSG00000109270 Protein coding 3'UTR GSE100210;GSE107867;GSE107867;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;ASD brains,cerebellum;ASD brains,frontal_cortex;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,30559470,30559470,31158229,31158229 RNA-Seq:(High) rs1337862066 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_7250647 20957 RMVar_ID_20957 Human_SNP_ID_196119675 A-to-I Human chr4 - 99881022 99881022 99881022 CTGGAAAAGAAACCTGAGATTGCAGTCAGCCAAGATTGTGCCACTGCACCCCAGCCTGGGCAACA CTGGAAAAGAAACCTGAGATTGCAGTCAGCCAGGATTGTGCCACTGCACCCCAGCCTGGGCAACA T C LAMTOR3 Ensembl:ENSG00000109270 Protein coding 3'UTR GSE38233;GSE100210;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,cerebellum - 24183664,29129909,30559470 RNA-Seq:(High) rs955672064 Functional Loss SNV dbSNP153 33..33 33 - - - 20958 RMVar_ID_20958 Human_SNP_ID_196400437 A-to-I Human chr4 - 101073415 101073415 101073415 AAAATTAGCCAGGTGTGGTGGCCCGCACCTGTAGTCCCAACTATTCGGGAGGCAGAGGAGGAAGA AAAATTAGCCAGGTGTGGTGGCCCGCACCTGTGGTCCCAACTATTCGGGAGGCAGAGGAGGAAGA T C PPP3CA Ensembl:ENSG00000138814 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1377140230 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3382,RMVar_hsa_circ_227660,RMVar_hsa_circ_76648,RMVar_hsa_circ_57237,RMVar_hsa_circ_331856,RMVar_hsa_circ_71686,RMVar_hsa_circ_227663,RMVar_hsa_circ_283403,RMVar_hsa_circ_304135,RMVar_hsa_circ_355527,RMVar_hsa_circ_376627,RMVar_hsa_circ_338954,RMVar_hsa_circ_303790,RMVar_hsa_circ_227661,RMVar_hsa_circ_341625,RMVar_hsa_circ_295029,RMVar_hsa_circ_21628,RMVar_hsa_circ_227664,RMVar_hsa_circ_227665,RMVar_hsa_circ_227662 20959 RMVar_ID_20959 Human_SNP_ID_196691358 A-to-I Human chr4 - 102259679 102259679 102259679 AGGGCCCTACTAAGTAACCAGAGATCATCATAATACTATTCAGGGACTATTAAAATCGTTGACTT AGGGCCCTACTAAGTAACCAGAGATCATCATACTACTATTCAGGGACTATTAAAATCGTTGACTT T G SLC39A8 Ensembl:ENSG00000138821 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs747566011 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47854,RMVar_hsa_circ_291224 20960 RMVar_ID_20960 Human_SNP_ID_196762560 A-to-I Human chr4 + 102558720 102558720 102558720 TTGCCCAGGCTGGAGTGCAGTGGTGCGATCATAGCCCAATGCCACCTTGAACTTCTGGGCTCAAA TTGCCCAGGCTGGAGTGCAGTGGTGCGATCATCGCCCAATGCCACCTTGAACTTCTGGGCTCAAA A C NFKB1 Ensembl:ENSG00000109320 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1269271748 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1152,RMVar_hsa_circ_125919,RMVar_hsa_circ_38757,RMVar_hsa_circ_227691,RMVar_hsa_circ_98005,RMVar_hsa_circ_284181,RMVar_hsa_circ_227696,RMVar_hsa_circ_227697,RMVar_hsa_circ_3620,RMVar_hsa_circ_266074,RMVar_hsa_circ_376795,RMVar_hsa_circ_347131,RMVar_hsa_circ_322262,RMVar_hsa_circ_227699,RMVar_hsa_circ_98801 20961 RMVar_ID_20961 Human_SNP_ID_196762571 A-to-I Human chr4 + 102558790 102558790 102558790 CTCCTACCTCAGTCTCCCAAGTAGCCGGAACTACAGGTGCACACTACCACACCCAGCTTCCCCAC CTCCTACCTCAGTCTCCCAAGTAGCCGGAACTGCAGGTGCACACTACCACACCCAGCTTCCCCAC A G NFKB1 Ensembl:ENSG00000109320 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs572009478 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1152,RMVar_hsa_circ_125919,RMVar_hsa_circ_38757,RMVar_hsa_circ_227691,RMVar_hsa_circ_98005,RMVar_hsa_circ_284181,RMVar_hsa_circ_227696,RMVar_hsa_circ_227697,RMVar_hsa_circ_3620,RMVar_hsa_circ_266074,RMVar_hsa_circ_376795,RMVar_hsa_circ_347131,RMVar_hsa_circ_322262,RMVar_hsa_circ_227699,RMVar_hsa_circ_98801 20962 RMVar_ID_20962 Human_SNP_ID_196784565 A-to-I Human chr4 - 102653930 102653930 102653930 GCAATAATTCAGTAAATATTCTTGCTTCCTTCATTCCTTCCTTCCCATTCTCGACAATAAGTAGC GCAATAATTCAGTAAATATTCTTGCTTCCTTCCTTCCTTCCTTCCCATTCTCGACAATAAGTAGC T G MANBA Ensembl:ENSG00000109323 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1419528924 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_855,RMVar_hsa_circ_12831,RMVar_hsa_circ_23791,RMVar_hsa_circ_227708,RMVar_hsa_circ_227710,RMVar_hsa_circ_282224,RMVar_hsa_circ_308779,RMVar_hsa_circ_367419,RMVar_hsa_circ_300803,RMVar_hsa_circ_273235,RMVar_hsa_circ_227709,RMVar_hsa_circ_227706,RMVar_hsa_circ_227707 20963 RMVar_ID_20963 Human_SNP_ID_196803672 A-to-I Human chr4 - 102734506 102734506 102734506 CAGCACTTCTGAGCTCAGATGGTTCAGCCTCCACCTCGTGGAACTTGGGAATGGGTATGATGATG CAGCACTTCTGAGCTCAGATGGTTCAGCCTCCGCCTCGTGGAACTTGGGAATGGGTATGATGATG T C MANBA Ensembl:ENSG00000109323 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1463132788 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_587600 RMVar_hsa_circ_227727,RMVar_hsa_circ_111245,RMVar_hsa_circ_227725,RMVar_hsa_circ_227726,RMVar_hsa_circ_227733 20964 RMVar_ID_20964 Human_SNP_ID_196807576 A-to-I Human chr4 + 102752063 102752060 102752063 GATGCTAAAGATCTGGTCTACAGTCCCTACAGAAGAAGAAGATGAAATGGAGGAATCCACAAATC GATGCTAAAGATCTGGTCTACAGTCCCTAC___AGAAGAAGATGAAATGGAGGAATCCACAAATC CAGA C AC018797.2 Ensembl:ENSG00000251288 Pseudogene exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1165590427 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_8266067 20965 RMVar_ID_20965 Human_SNP_ID_196807984 A-to-I Human chr4 - 102753947 102753947 102753947 CCAGGTTGGAGTGAAGTGGCATCATCTTCCTCACTGCATTCTCTGCCTCCCAGGTTCAAGCGATT CCAGGTTGGAGTGAAGTGGCATCATCTTCCTCGCTGCATTCTCTGCCTCCCAGGTTCAAGCGATT T C MANBA Ensembl:ENSG00000109323 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs765208633 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_610361,Human_RBP_ID_17406786 Human_Splice_Rec_587606,Human_Splice_Rec_587612 RMVar_hsa_circ_111245,RMVar_hsa_circ_227725 20966 RMVar_ID_20966 Human_SNP_ID_196817446 A-to-I Human chr4 - 102791705 102791705 102791705 TGATACACCCCTCGACCTCCTGGACTCAAGCAATCCTCCCACCTCAGCCTCCTGAGTAGTTGGGG TGATACACCCCTCGACCTCCTGGACTCAAGCAGTCCTCCCACCTCAGCCTCCTGAGTAGTTGGGG T C - - Other Unknown GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs531144315 Functional Loss SNV dbSNP153 33..33 33 - - - 20967 RMVar_ID_20967 Human_SNP_ID_196823258 A-to-I Human chr4 - 102811494 102811489 102811495 TGATGTTAGTAGAGATGGGGTTTTACCATGTTAGCAGCACTGGTCTTGAACTCCTGACCTTAGGT TGATGTTAGTAGAGATGGGGTTTTACCATGT______CACTGGTCTTGAACTCCTGACCTTAGGT GCTGCTA G UBE2D3 Ensembl:ENSG00000109332 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1387563685 Functional Loss DEL dbSNP153 32..37 33 - - - Human_RBP_ID_7252336,Human_RBP_ID_15013406 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_2782 20968 RMVar_ID_20968 Human_SNP_ID_196823397 A-to-I Human chr4 - 102811824 102811824 102811824 TTATGGAGAATGGGGTCTCACTATGTTATCCAAGCTGGTCTCGAACTCCTGCGCTCAAGCTGTCC TTATGGAGAATGGGGTCTCACTATGTTATCCAGGCTGGTCTCGAACTCCTGCGCTCAAGCTGTCC T C UBE2D3 Ensembl:ENSG00000109332 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1364454971 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7252345,Human_RBP_ID_15013414 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_2782 20969 RMVar_ID_20969 Human_SNP_ID_196824314 A-to-I Human chr4 - 102815155 102815155 102815155 TCTCTAGTTCCAGTTACTCGGAAGGCTGAGGCAGGAGAATCACTTGAACCCAGGAGGCAGAGGTT TCTCTAGTTCCAGTTACTCGGAAGGCTGAGGCCGGAGAATCACTTGAACCCAGGAGGCAGAGGTT T G UBE2D3 Ensembl:ENSG00000109332 Protein coding intron GSE107867 ASD brains,frontal_cortex;ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1034613593 Functional Loss SNV dbSNP153 33..33 33 - - - 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_2782 20970 RMVar_ID_20970 Human_SNP_ID_196837520 A-to-I Human chr4 - 102867778 102867778 102867778 TTGTTGTTGTTGTTGTTACAAGGTTTCGCTCTATCGCCCAGGCTGTAGTGCAGTGGTCAGATCAT TTGTTGTTGTTGTTGTTACAAGGTTTCGCTCTGTCGCCCAGGCTGTAGTGCAGTGGTCAGATCAT T C UBE2D3 Ensembl:ENSG00000109332 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1012556399 Functional Loss SNV dbSNP153 33..33 33 - - - 20971 RMVar_ID_20971 Human_SNP_ID_196841031 A-to-I Human chr4 + 102882045 102882045 102882045 GAAACCCCATCTCTACTAAAAATACAAAAATTAGCCAGACGTTGTGGTGTGCTCCTGCAGTTTTA GAAACCCCATCTCTACTAAAAATACAAAAATTTGCCAGACGTTGTGGTGTGCTCCTGCAGTTTTA A T CISD2 Ensembl:ENSG00000145354 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs987216142 Functional Loss SNV dbSNP153 33..33 33 - - - 20972 RMVar_ID_20972 Human_SNP_ID_196841041 A-to-I Human chr4 + 102882071 102882071 102882071 AAAATTAGCCAGACGTTGTGGTGTGCTCCTGCAGTTTTAGTTACTTGGGAGGCTGAGGCAGGAGG AAAATTAGCCAGACGTTGTGGTGTGCTCCTGCGGTTTTAGTTACTTGGGAGGCTGAGGCAGGAGG A G CISD2 Ensembl:ENSG00000145354 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1254741982 Functional Loss SNV dbSNP153 33..33 33 - - - 20973 RMVar_ID_20973 Human_SNP_ID_196842064 A-to-I Human chr4 + 102886862 102886862 102886862 GTCTTGAACTCCTGATGTCAAGTGATTTGTCTACCTCTGCCTCTGAAAGTGTTGGGATTACAGGC GTCTTGAACTCCTGATGTCAAGTGATTTGTCTCCCTCTGCCTCTGAAAGTGTTGGGATTACAGGC A C CISD2 Ensembl:ENSG00000145354 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992928412 Functional Loss SNV dbSNP153 33..33 33 - - - 20974 RMVar_ID_20974 Human_SNP_ID_196842065 A-to-I Human chr4 + 102886862 102886862 102886862 GTCTTGAACTCCTGATGTCAAGTGATTTGTCTACCTCTGCCTCTGAAAGTGTTGGGATTACAGGC GTCTTGAACTCCTGATGTCAAGTGATTTGTCTGCCTCTGCCTCTGAAAGTGTTGGGATTACAGGC A G CISD2 Ensembl:ENSG00000145354 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992928412 Functional Loss SNV dbSNP153 33..33 33 - - - 20975 RMVar_ID_20975 Human_SNP_ID_196882468 A-to-I Human chr4 - 103062164 103062164 103062164 CCTGCCTCGGCGTCTCCCAAAGCGCTGGGATTACAGGCGTGAGCCACTGCGCCCAGCCGAAAAGA CCTGCCTCGGCGTCTCCCAAAGCGCTGGGATTGCAGGCGTGAGCCACTGCGCCCAGCCGAAAAGA T C SLC9B2 Ensembl:ENSG00000164038 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1228537900 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25774113 RMVar_hsa_circ_296933,RMVar_hsa_circ_227758 20976 RMVar_ID_20976 Human_SNP_ID_196882472 A-to-I Human chr4 - 103062177 103062177 103062177 ACCTCATGATCCGCCTGCCTCGGCGTCTCCCAAAGCGCTGGGATTACAGGCGTGAGCCACTGCGC ACCTCATGATCCGCCTGCCTCGGCGTCTCCCAGAGCGCTGGGATTACAGGCGTGAGCCACTGCGC T C SLC9B2 Ensembl:ENSG00000164038 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1443341900 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_296933,RMVar_hsa_circ_227758 20977 RMVar_ID_20977 Human_SNP_ID_196882473 A-to-I Human chr4 - 103062177 103062177 103062177 ACCTCATGATCCGCCTGCCTCGGCGTCTCCCAAAGCGCTGGGATTACAGGCGTGAGCCACTGCGC ACCTCATGATCCGCCTGCCTCGGCGTCTCCCACAGCGCTGGGATTACAGGCGTGAGCCACTGCGC T G SLC9B2 Ensembl:ENSG00000164038 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1443341900 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_296933,RMVar_hsa_circ_227758 20978 RMVar_ID_20978 Human_SNP_ID_196882485 A-to-I Human chr4 - 103062204 103062204 103062204 GTTGGTCAGGCTGGTCTCGAACTTCTGACCTCATGATCCGCCTGCCTCGGCGTCTCCCAAAGCGC GTTGGTCAGGCTGGTCTCGAACTTCTGACCTCGTGATCCGCCTGCCTCGGCGTCTCCCAAAGCGC T C SLC9B2 Ensembl:ENSG00000164038 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928841356 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_296933,RMVar_hsa_circ_227758 20979 RMVar_ID_20979 Human_SNP_ID_196882499 A-to-I Human chr4 - 103062238 103062238 103062238 ATTTTTGTATTTAGTAGAGACGGGGTTTCACCATGTTGGTCAGGCTGGTCTCGAACTTCTGACCT ATTTTTGTATTTAGTAGAGACGGGGTTTCACCCTGTTGGTCAGGCTGGTCTCGAACTTCTGACCT T G SLC9B2 Ensembl:ENSG00000164038 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs947413684 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_296933,RMVar_hsa_circ_227758 20980 RMVar_ID_20980 Human_SNP_ID_196882506 A-to-I Human chr4 - 103062255 103062255 103062255 GCCACCATGCCCGGCTAATTTTTGTATTTAGTAGAGACGGGGTTTCACCATGTTGGTCAGGCTGG GCCACCATGCCCGGCTAATTTTTGTATTTAGTGGAGACGGGGTTTCACCATGTTGGTCAGGCTGG T C SLC9B2 Ensembl:ENSG00000164038 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1395254569 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_296933,RMVar_hsa_circ_227758 20981 RMVar_ID_20981 Human_SNP_ID_196882520 A-to-I Human chr4 - 103062297 103062297 103062297 CTCCTTCCTCAGCCTCCTGAATAGCTGGGATTACAGGCACGTGCCACCATGCCCGGCTAATTTTT CTCCTTCCTCAGCCTCCTGAATAGCTGGGATTGCAGGCACGTGCCACCATGCCCGGCTAATTTTT T C SLC9B2 Ensembl:ENSG00000164038 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs191264305 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_296933,RMVar_hsa_circ_227758 20982 RMVar_ID_20982 Human_SNP_ID_196882635 A-to-I Human chr4 - 103062716 103062716 103062716 ATTGCAGCTACTTAGGAGGCTGAGACAGGAGAATCACTTGAACCTGGGAGGCGGAGGTTGAGATC ATTGCAGCTACTTAGGAGGCTGAGACAGGAGAGTCACTTGAACCTGGGAGGCGGAGGTTGAGATC T C SLC9B2 Ensembl:ENSG00000164038 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs545331967 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_296933,RMVar_hsa_circ_227758 20983 RMVar_ID_20983 Human_SNP_ID_196882656 A-to-I Human chr4 - 103062811 103062811 103062811 GGTCAGGAGTTCAAGACCAGCCTGGCTAACATAGTGAAACCTCATCTCCACTAAAAATACAAAAA GGTCAGGAGTTCAAGACCAGCCTGGCTAACATGGTGAAACCTCATCTCCACTAAAAATACAAAAA T C SLC9B2 Ensembl:ENSG00000164038 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs949561587 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_296933,RMVar_hsa_circ_227758 20984 RMVar_ID_20984 Human_SNP_ID_197014352 A-to-I Human chr4 - 103572607 103572607 103572607 ACATCACTGAAACTTTCAATATGTGGAGGACAATTGCTGTCTGTTGCCTCAACTAGAATGTCATC ACATCACTGAAACTTTCAATATGTGGAGGACAGTTGCTGTCTGTTGCCTCAACTAGAATGTCATC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1481857970 Functional Loss SNV dbSNP153 33..33 33 - - - 20985 RMVar_ID_20985 Human_SNP_ID_197014693 A-to-I Human chr4 + 103573990 103573987 103573990 CACAGTGGTGAAGGTGGCCACGGCAGCAGCAGAAGATTTGGTGGAGGTGGCTATGGAGGCTTTTG CACAGTGGTGAAGGTGGCCACGGCAGCAGC___AGATTTGGTGGAGGTGGCTATGGAGGCTTTTG CAGA C AC105460.2,DDX3P3 Ensembl:ENSG00000251577,Ensembl:ENSG00000251571 lincRNA,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1279581664 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_4796261,Human_RBP_ID_7342726,Human_RBP_ID_8265912,Human_RBP_ID_8876297,Human_RBP_ID_23028062 20986 RMVar_ID_20986 Human_SNP_ID_197014694 A-to-I Human chr4 + 103573990 103573990 103573990 CACAGTGGTGAAGGTGGCCACGGCAGCAGCAGAAGATTTGGTGGAGGTGGCTATGGAGGCTTTTG CACAGTGGTGAAGGTGGCCACGGCAGCAGCAGCAGATTTGGTGGAGGTGGCTATGGAGGCTTTTG A C AC105460.2,DDX3P3 Ensembl:ENSG00000251577,Ensembl:ENSG00000251571 lincRNA,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs2757675 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4796261,Human_RBP_ID_7342726,Human_RBP_ID_8265912,Human_RBP_ID_8876297,Human_RBP_ID_23028062 GWAS_ID_1930,GWAS_ID_1931 20987 RMVar_ID_20987 Human_SNP_ID_522554047 A-to-I Human chr13 - 18892463 18892463 18892463 TGCAGAGCCTAATGGGAGTCCTCCCAGATCTCATAGTAGAAATTCTTGGGGTGAACAAATGCCAG TGCAGAGCCTAATGGGAGTCCTCCCAGATCTCGTAGTAGAAATTCTTGGGGTGAACAAATGCCAG T C SNX19P2 Ensembl:ENSG00000235500 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256524675 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8249089 20988 RMVar_ID_20988 Human_SNP_ID_522679014 A-to-I Human chr13 + 19305041 19305041 19305041 TTTGGCTGTGACATCCACATACTGTCCTGGACAAAAGTGAGCAGCATAAAGAGGAGTGCCTGGTT TTTGGCTGTGACATCCACATACTGTCCTGGACGAAAGTGAGCAGCATAAAGAGGAGTGCCTGGTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879057387 Functional Loss SNV dbSNP153 33..33 33 - - - 20989 RMVar_ID_20989 Human_SNP_ID_522754692 A-to-I Human chr13 + 19621849 19621849 19621849 CTTCAGATGCTCTGAAAGTCTTAATATGGGCCAGGCATGGTGGCTCACACCTGTAATCTCAGCAC CTTCAGATGCTCTGAAAGTCTTAATATGGGCCGGGCATGGTGGCTCACACCTGTAATCTCAGCAC A G lnc-MPHOSPH8-5,lnc-MPHOSPH8-5:2,lnc-MPHOSPH8-5:3 RNACentral:URS00009B128E,RNACentral:URS00009C5C77,RNACentral:URS00008B4002 lincRNA,lincRNA,lincRNA intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1046388580 Functional Loss SNV dbSNP153 33..33 33 - - - 20990 RMVar_ID_20990 Human_SNP_ID_522768012 A-to-I Human chr13 + 19670913 19670913 19670913 CGGATTACAGCTCACTGGAGTCTTGACTTCCCAGGCACAAGCAATCCTCCCACCTCAGCCTCCTA CGGATTACAGCTCACTGGAGTCTTGACTTCCCGGGCACAAGCAATCCTCCCACCTCAGCCTCCTA A G MPHOSPH8 Ensembl:ENSG00000196199 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1258613581 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1448942,Human_Splice_Rec_1448946 RMVar_hsa_circ_161943,RMVar_hsa_circ_111206,RMVar_hsa_circ_32944 20991 RMVar_ID_20991 Human_SNP_ID_522768307 A-to-I Human chr13 + 19671871 19671870 19671871 GTTGCTAATAGGTGCATACAGAGTGCAGCTGCAGTGACCAAACAGAAGGGACTGGGCGGAGTTCT GTTGCTAATAGGTGCATACAGAGTGCAGCTGC_GTGACCAAACAGAAGGGACTGGGCGGAGTTCT CA C MPHOSPH8 Ensembl:ENSG00000196199 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs763330382 Functional Loss DEL dbSNP153 33..33 33 - - - Human_Splice_Rec_1448930,Human_Splice_Rec_1448944,Human_Splice_Rec_1448948 RMVar_hsa_circ_161949 20992 RMVar_ID_20992 Human_SNP_ID_522768414 A-to-I Human chr13 + 19672219 19672219 19672219 CAGGCTGGAGTGCAATGGTGCGATCTCGGCTCACTGCAAGCTCTGCCTCCTGGGTTCAAGTGATT CAGGCTGGAGTGCAATGGTGCGATCTCGGCTCGCTGCAAGCTCTGCCTCCTGGGTTCAAGTGATT A G MPHOSPH8 Ensembl:ENSG00000196199 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1128241 Functional Loss SNV dbSNP153 33..33 33 - - - 20993 RMVar_ID_20993 Human_SNP_ID_522768424 A-to-I Human chr13 + 19672262 19672262 19672262 TGCCTCCTGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGACACCCG TGCCTCCTGGGTTCAAGTGATTCTCCTGCCTCGGCCTCCTGAGTAGCTGGGATTACAGACACCCG A G MPHOSPH8 Ensembl:ENSG00000196199 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1128242 Functional Loss SNV dbSNP153 33..33 33 - - - 20994 RMVar_ID_20994 Human_SNP_ID_522768463 A-to-I Human chr13 + 19672378 19672378 19672378 GTTGGTCAGGCTGGTCTTGAACTCCTGACCTCAGGTGATCCGCCCGCCTCGGCCTCCCAAAGTGC GTTGGTCAGGCTGGTCTTGAACTCCTGACCTCGGGTGATCCGCCCGCCTCGGCCTCCCAAAGTGC A G MPHOSPH8 Ensembl:ENSG00000196199 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs931593127 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26426521 20995 RMVar_ID_20995 Human_SNP_ID_522768613 A-to-I Human chr13 + 19672842 19672842 19672842 GAACTTTTAGCAGAGCGTGGTGGCTCACACCTATAATCCCAGCGCTTTGGAGGCTGAGGTTGGAG GAACTTTTAGCAGAGCGTGGTGGCTCACACCTGTAATCCCAGCGCTTTGGAGGCTGAGGTTGGAG A G MPHOSPH8 Ensembl:ENSG00000196199 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs376764760 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_756282,Human_RBP_ID_26426524 20996 RMVar_ID_20996 Human_SNP_ID_522768623 A-to-I Human chr13 + 19672883 19672883 19672883 GCGCTTTGGAGGCTGAGGTTGGAGGATTGCTTAAGTCCAGGAGTTCAAGACCAGCCTGGGTAACA GCGCTTTGGAGGCTGAGGTTGGAGGATTGCTTGAGTCCAGGAGTTCAAGACCAGCCTGGGTAACA A G MPHOSPH8 Ensembl:ENSG00000196199 Protein coding 3'UTR GSE38233;GSE100210;GSE100210;GSE99789;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;HepG2 cell line;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,29129909,29796672,29796672,31158229,31158229,31158229,31158229,31158229,32596459,32596459,32596459 RNA-Seq:(High) rs1460978065 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26426525 20997 RMVar_ID_20997 Human_SNP_ID_522768667 A-to-I Human chr13 + 19673031 19673030 19673031 TGAGCCGTGAAAGGCCACTGCACTCCAGCCTGAGTGACAGAATGAGACCTTGTCTCAAAAAAAAA TGAGCCGTGAAAGGCCACTGCACTCCAGCCTG_GTGACAGAATGAGACCTTGTCTCAAAAAAAAA GA G MPHOSPH8 Ensembl:ENSG00000196199 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1413462518 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_26424693 20998 RMVar_ID_20998 Human_SNP_ID_522768668 A-to-I Human chr13 + 19673031 19673031 19673031 TGAGCCGTGAAAGGCCACTGCACTCCAGCCTGAGTGACAGAATGAGACCTTGTCTCAAAAAAAAA TGAGCCGTGAAAGGCCACTGCACTCCAGCCTGGGTGACAGAATGAGACCTTGTCTCAAAAAAAAA A G MPHOSPH8 Ensembl:ENSG00000196199 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4769866 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26424693 20999 RMVar_ID_20999 Human_SNP_ID_522771011 A-to-I Human chr13 - 19681075 19681075 19681075 AAGTAGCCAGGACGACCTGTGTGTGCCACCGCACTCAGCTAATTTTTACATTTTTTGTAGAGTCA AAGTAGCCAGGACGACCTGTGTGTGCCACCGCCCTCAGCTAATTTTTACATTTTTTGTAGAGTCA T G PSPC1 Ensembl:ENSG00000121390 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167638263 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16518 21000 RMVar_ID_21000 Human_SNP_ID_522780409 A-to-I Human chr13 - 19714768 19714768 19714768 TGGGTTGGCTGGGCATGGTGGCTCACACCTGTAATCACAGCACTTTGGGGGGTTGAGGCAGGTGG TGGGTTGGCTGGGCATGGTGGCTCACACCTGTCATCACAGCACTTTGGGGGGTTGAGGCAGGTGG T G PSPC1 Ensembl:ENSG00000121390 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1259785505 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12109102 RMVar_hsa_circ_94389,RMVar_hsa_circ_16518,RMVar_hsa_circ_117908,RMVar_hsa_circ_161951,RMVar_hsa_circ_161952,RMVar_hsa_circ_369512,RMVar_hsa_circ_371762,RMVar_hsa_circ_161954,RMVar_hsa_circ_161955,RMVar_hsa_circ_161956,RMVar_hsa_circ_317546 21001 RMVar_ID_21001 Human_SNP_ID_522788869 A-to-I Human chr13 - 19744784 19744784 19744784 CCAAGGCGGGTGGATCACAAGGTTACGAGTTCAAGACCAGCCTGGCCAAGATGGTGAAACCTCAT CCAAGGCGGGTGGATCACAAGGTTACGAGTTCGAGACCAGCCTGGCCAAGATGGTGAAACCTCAT T C PSPC1 Ensembl:ENSG00000121390 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1355239999 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94389,RMVar_hsa_circ_16518,RMVar_hsa_circ_117908,RMVar_hsa_circ_161957,RMVar_hsa_circ_161951,RMVar_hsa_circ_161952,RMVar_hsa_circ_369512,RMVar_hsa_circ_161955,RMVar_hsa_circ_288460,RMVar_hsa_circ_161956,RMVar_hsa_circ_317546,RMVar_hsa_circ_342831,RMVar_hsa_circ_45851,RMVar_hsa_circ_80206,RMVar_hsa_circ_161958,RMVar_hsa_circ_161959,RMVar_hsa_circ_161961,RMVar_hsa_circ_318374,RMVar_hsa_circ_338892,RMVar_hsa_circ_340427,RMVar_hsa_circ_294847,RMVar_hsa_circ_161963,RMVar_hsa_circ_161964,RMVar_hsa_circ_161962 21002 RMVar_ID_21002 Human_SNP_ID_522788960 A-to-I Human chr13 - 19745083 19745083 19745083 AAACTCCTGACCTCAAGTGATCCACCCGCCTCAGCCTCCCAAAGTGCTGGGATTACTTTCGGAGG AAACTCCTGACCTCAAGTGATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTACTTTCGGAGG T C PSPC1 Ensembl:ENSG00000121390 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs188392372 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94389,RMVar_hsa_circ_16518,RMVar_hsa_circ_117908,RMVar_hsa_circ_161957,RMVar_hsa_circ_161951,RMVar_hsa_circ_161952,RMVar_hsa_circ_369512,RMVar_hsa_circ_161955,RMVar_hsa_circ_288460,RMVar_hsa_circ_161956,RMVar_hsa_circ_317546,RMVar_hsa_circ_342831,RMVar_hsa_circ_45851,RMVar_hsa_circ_80206,RMVar_hsa_circ_161958,RMVar_hsa_circ_161959,RMVar_hsa_circ_161961,RMVar_hsa_circ_318374,RMVar_hsa_circ_338892,RMVar_hsa_circ_340427,RMVar_hsa_circ_294847,RMVar_hsa_circ_161963,RMVar_hsa_circ_161964,RMVar_hsa_circ_161962 21003 RMVar_ID_21003 Human_SNP_ID_522788993 A-to-I Human chr13 - 19745206 19745206 19745206 CAAGTGATTCTTCTGCCTCATCCTCCTTGAGTAGCTGGGACTACAGGCGTGTGCCACCATGCCCG CAAGTGATTCTTCTGCCTCATCCTCCTTGAGTGGCTGGGACTACAGGCGTGTGCCACCATGCCCG T C PSPC1 Ensembl:ENSG00000121390 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1388047010 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94389,RMVar_hsa_circ_16518,RMVar_hsa_circ_117908,RMVar_hsa_circ_161957,RMVar_hsa_circ_161951,RMVar_hsa_circ_161952,RMVar_hsa_circ_369512,RMVar_hsa_circ_161955,RMVar_hsa_circ_288460,RMVar_hsa_circ_161956,RMVar_hsa_circ_317546,RMVar_hsa_circ_342831,RMVar_hsa_circ_45851,RMVar_hsa_circ_80206,RMVar_hsa_circ_161958,RMVar_hsa_circ_161959,RMVar_hsa_circ_161961,RMVar_hsa_circ_318374,RMVar_hsa_circ_338892,RMVar_hsa_circ_340427,RMVar_hsa_circ_294847,RMVar_hsa_circ_161963,RMVar_hsa_circ_161964,RMVar_hsa_circ_161962 21004 RMVar_ID_21004 Human_SNP_ID_522789790 A-to-I Human chr13 - 19748051 19748051 19748051 ACACCACCACGCCCAGCTAATTTTGTATTTTTAGTAGAGATGGGGTTTCATCATGTTGGTCAAGC ACACCACCACGCCCAGCTAATTTTGTATTTTTGGTAGAGATGGGGTTTCATCATGTTGGTCAAGC T C PSPC1 Ensembl:ENSG00000121390 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1177055835 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94389,RMVar_hsa_circ_16518,RMVar_hsa_circ_117908,RMVar_hsa_circ_161957,RMVar_hsa_circ_161951,RMVar_hsa_circ_161952,RMVar_hsa_circ_369512,RMVar_hsa_circ_161955,RMVar_hsa_circ_288460,RMVar_hsa_circ_161956,RMVar_hsa_circ_317546,RMVar_hsa_circ_342831,RMVar_hsa_circ_45851,RMVar_hsa_circ_80206,RMVar_hsa_circ_161958,RMVar_hsa_circ_161959,RMVar_hsa_circ_161961,RMVar_hsa_circ_318374,RMVar_hsa_circ_338892,RMVar_hsa_circ_340427,RMVar_hsa_circ_294847,RMVar_hsa_circ_161963,RMVar_hsa_circ_161964,RMVar_hsa_circ_161962 21005 RMVar_ID_21005 Human_SNP_ID_522791267 A-to-I Human chr13 - 19753171 19753171 19753171 TCAAGCGATTCTCCTGCCTTAGCCTCCTGAGTAGCTGGGATCGCAGGCACCCGCCACCACGCCTG TCAAGCGATTCTCCTGCCTTAGCCTCCTGAGTGGCTGGGATCGCAGGCACCCGCCACCACGCCTG T C PSPC1 Ensembl:ENSG00000121390 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs548184314 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94389,RMVar_hsa_circ_16518,RMVar_hsa_circ_117908,RMVar_hsa_circ_161957,RMVar_hsa_circ_161951,RMVar_hsa_circ_161952,RMVar_hsa_circ_369512,RMVar_hsa_circ_161955,RMVar_hsa_circ_288460,RMVar_hsa_circ_161956,RMVar_hsa_circ_317546,RMVar_hsa_circ_342831,RMVar_hsa_circ_80206,RMVar_hsa_circ_161958,RMVar_hsa_circ_161959,RMVar_hsa_circ_318374,RMVar_hsa_circ_338892,RMVar_hsa_circ_294847,RMVar_hsa_circ_161963,RMVar_hsa_circ_161964,RMVar_hsa_circ_161962,RMVar_hsa_circ_274847,RMVar_hsa_circ_320745 21006 RMVar_ID_21006 Human_SNP_ID_522792266 A-to-I Human chr13 - 19756965 19756965 19756965 CCACCATGCCCGGCTAATTTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGA CCACCATGCCCGGCTAATTTTTTTGTATTTTTGGTAGAGACGGGGTTTCACCGTGTTAGCCAGGA T C PSPC1 Ensembl:ENSG00000121390 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs962868355 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94389,RMVar_hsa_circ_16518,RMVar_hsa_circ_117908,RMVar_hsa_circ_161957,RMVar_hsa_circ_161951,RMVar_hsa_circ_161952,RMVar_hsa_circ_369512,RMVar_hsa_circ_161955,RMVar_hsa_circ_288460,RMVar_hsa_circ_161956,RMVar_hsa_circ_317546,RMVar_hsa_circ_342831,RMVar_hsa_circ_80206,RMVar_hsa_circ_161958,RMVar_hsa_circ_161959,RMVar_hsa_circ_318374,RMVar_hsa_circ_338892,RMVar_hsa_circ_294847,RMVar_hsa_circ_161963,RMVar_hsa_circ_161964,RMVar_hsa_circ_161962,RMVar_hsa_circ_274847,RMVar_hsa_circ_320745 21007 RMVar_ID_21007 Human_SNP_ID_522792267 A-to-I Human chr13 - 19756965 19756965 19756965 CCACCATGCCCGGCTAATTTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGA CCACCATGCCCGGCTAATTTTTTTGTATTTTTCGTAGAGACGGGGTTTCACCGTGTTAGCCAGGA T G PSPC1 Ensembl:ENSG00000121390 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs962868355 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94389,RMVar_hsa_circ_16518,RMVar_hsa_circ_117908,RMVar_hsa_circ_161957,RMVar_hsa_circ_161951,RMVar_hsa_circ_161952,RMVar_hsa_circ_369512,RMVar_hsa_circ_161955,RMVar_hsa_circ_288460,RMVar_hsa_circ_161956,RMVar_hsa_circ_317546,RMVar_hsa_circ_342831,RMVar_hsa_circ_80206,RMVar_hsa_circ_161958,RMVar_hsa_circ_161959,RMVar_hsa_circ_318374,RMVar_hsa_circ_338892,RMVar_hsa_circ_294847,RMVar_hsa_circ_161963,RMVar_hsa_circ_161964,RMVar_hsa_circ_161962,RMVar_hsa_circ_274847,RMVar_hsa_circ_320745 21008 RMVar_ID_21008 Human_SNP_ID_522792271 A-to-I Human chr13 - 19756982 19756982 19756982 GGGACTGTAGGCACGTGCCACCATGCCCGGCTAATTTTTTTGTATTTTTAGTAGAGACGGGGTTT GGGACTGTAGGCACGTGCCACCATGCCCGGCTGATTTTTTTGTATTTTTAGTAGAGACGGGGTTT T C PSPC1 Ensembl:ENSG00000121390 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1311193447 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94389,RMVar_hsa_circ_16518,RMVar_hsa_circ_117908,RMVar_hsa_circ_161957,RMVar_hsa_circ_161951,RMVar_hsa_circ_161952,RMVar_hsa_circ_369512,RMVar_hsa_circ_161955,RMVar_hsa_circ_288460,RMVar_hsa_circ_161956,RMVar_hsa_circ_317546,RMVar_hsa_circ_342831,RMVar_hsa_circ_80206,RMVar_hsa_circ_161958,RMVar_hsa_circ_161959,RMVar_hsa_circ_318374,RMVar_hsa_circ_338892,RMVar_hsa_circ_294847,RMVar_hsa_circ_161963,RMVar_hsa_circ_161964,RMVar_hsa_circ_161962,RMVar_hsa_circ_274847,RMVar_hsa_circ_320745 21009 RMVar_ID_21009 Human_SNP_ID_522793929 A-to-I Human chr13 - 19763296 19763296 19763296 AGTAACCTGGACAGACGTAGTCACTCATGCCTATAATCCCAGCACTTTGGGAGGCTGAAGCGAGA AGTAACCTGGACAGACGTAGTCACTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAAGCGAGA T C PSPC1 Ensembl:ENSG00000121390 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1179060416 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_161966,RMVar_hsa_circ_94389,RMVar_hsa_circ_117908,RMVar_hsa_circ_161957,RMVar_hsa_circ_161951,RMVar_hsa_circ_161952,RMVar_hsa_circ_369512,RMVar_hsa_circ_161955,RMVar_hsa_circ_288460,RMVar_hsa_circ_161956,RMVar_hsa_circ_317546,RMVar_hsa_circ_80206,RMVar_hsa_circ_161958,RMVar_hsa_circ_318374,RMVar_hsa_circ_338892,RMVar_hsa_circ_161963,RMVar_hsa_circ_161964,RMVar_hsa_circ_320745,RMVar_hsa_circ_161967,RMVar_hsa_circ_339366 21010 RMVar_ID_21010 Human_SNP_ID_522794658 A-to-I Human chr13 - 19765613 19765613 19765613 AATTAAAAAAATTAAAACAAGCTGAGTGTAGTAGTAGGCACCTGTAGTCCCAGCTACTCTGAAGG AATTAAAAAAATTAAAACAAGCTGAGTGTAGTGGTAGGCACCTGTAGTCCCAGCTACTCTGAAGG T C PSPC1 Ensembl:ENSG00000121390 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1365143893 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12109951 RMVar_hsa_circ_161966,RMVar_hsa_circ_94389,RMVar_hsa_circ_117908,RMVar_hsa_circ_161957,RMVar_hsa_circ_161951,RMVar_hsa_circ_161952,RMVar_hsa_circ_369512,RMVar_hsa_circ_161955,RMVar_hsa_circ_288460,RMVar_hsa_circ_161956,RMVar_hsa_circ_317546,RMVar_hsa_circ_80206,RMVar_hsa_circ_161958,RMVar_hsa_circ_318374,RMVar_hsa_circ_338892,RMVar_hsa_circ_161963,RMVar_hsa_circ_161964,RMVar_hsa_circ_320745,RMVar_hsa_circ_161967,RMVar_hsa_circ_339366 21011 RMVar_ID_21011 Human_SNP_ID_522798135 A-to-I Human chr13 - 19777905 19777905 19777905 GTCTCACTCTGTCGCCCAGGCTGGAGTGCAGTAGCGCGATCTCGACTCACTGCAACCTCTGCCTC GTCTCACTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCGATCTCGACTCACTGCAACCTCTGCCTC T C PSPC1 Ensembl:ENSG00000121390 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1362494959 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_161966,RMVar_hsa_circ_94389,RMVar_hsa_circ_117908,RMVar_hsa_circ_161957,RMVar_hsa_circ_161951,RMVar_hsa_circ_161952,RMVar_hsa_circ_369512,RMVar_hsa_circ_161955,RMVar_hsa_circ_288460,RMVar_hsa_circ_161956,RMVar_hsa_circ_317546,RMVar_hsa_circ_318374,RMVar_hsa_circ_161963,RMVar_hsa_circ_161964,RMVar_hsa_circ_320745,RMVar_hsa_circ_161967,RMVar_hsa_circ_339366,RMVar_hsa_circ_161969,RMVar_hsa_circ_290602,RMVar_hsa_circ_161970 21012 RMVar_ID_21012 Human_SNP_ID_522819326 A-to-I Human chr13 - 19853492 19853492 19853492 GCTCAGGGGTTCGAGACCAGCCTGGGCAACATAGTGAGACCTCACATCTACTAAAAGAAAAAAAA GCTCAGGGGTTCGAGACCAGCCTGGGCAACATGGTGAGACCTCACATCTACTAAAAGAAAAAAAA T C ZMYM5 Ensembl:ENSG00000132950 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs563949809 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_364424,RMVar_hsa_circ_335669 21013 RMVar_ID_21013 Human_SNP_ID_522819449 A-to-I Human chr13 - 19853868 19853868 19853868 TCAGAAAATTGAGGCCAGAGGCCAGGCCTGGTAGCTCACACCTATAATCCCAACACTTTGGGAGG TCAGAAAATTGAGGCCAGAGGCCAGGCCTGGTGGCTCACACCTATAATCCCAACACTTTGGGAGG T C ZMYM5 Ensembl:ENSG00000132950 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs536909071 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_364424,RMVar_hsa_circ_335669 21014 RMVar_ID_21014 Human_SNP_ID_522819576 A-to-I Human chr13 - 19854459 19854459 19854459 CACCACGACTGACTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCACGTTGACCAGGCTGA CACCACGACTGACTAATTTTTGTATTTTTAGTTGAGATGGGGTTTCACCACGTTGACCAGGCTGA T A ZMYM5 Ensembl:ENSG00000132950 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1270460871 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_364424,RMVar_hsa_circ_335669 21015 RMVar_ID_21015 Human_SNP_ID_522820554 A-to-I Human chr13 - 19858351 19858345 19858351 TGAACTCCTGGACTCAAGCGATCCACCTGCCTAGGCCTCCCAAAGCGCTGGGATTACAGGGGCAT TGAACTCCTGGACTCAAGCGATCCACCTGCCT______CCCAAAGCGCTGGGATTACAGGGGCAT GAGGCCT G ZMYM5 Ensembl:ENSG00000132950 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167648767 Functional Loss DEL dbSNP153 33..38 33 - - - RMVar_hsa_circ_364424,RMVar_hsa_circ_335669 21016 RMVar_ID_21016 Human_SNP_ID_522821032 A-to-I Human chr13 - 19859921 19859921 19859921 GTTGTATTTTTAGTAGAGACAAGGGACTGACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCT GTTGTATTTTTAGTAGAGACAAGGGACTGACCGTGTTGGCCAGGCTGGTCTCGAACTCCTGACCT T C ZMYM5 Ensembl:ENSG00000132950 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1182695555 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_364424,RMVar_hsa_circ_335669 21017 RMVar_ID_21017 Human_SNP_ID_522856630 A-to-I Human chr13 + 19985927 19985927 19985927 AGTAAAAAAGCCGGGTGTGATAACGTGCGCCTATAAATCCCAGCTACTCAGGAGGTTGAGGCAGG AGTAAAAAAGCCGGGTGTGATAACGTGCGCCTGTAAATCCCAGCTACTCAGGAGGTTGAGGCAGG A G ZMYM2 Ensembl:ENSG00000121741 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1301072993 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58596,RMVar_hsa_circ_309496,RMVar_hsa_circ_333442,RMVar_hsa_circ_361023,RMVar_hsa_circ_327279,RMVar_hsa_circ_299106,RMVar_hsa_circ_307113,RMVar_hsa_circ_298074,RMVar_hsa_circ_39232,RMVar_hsa_circ_161988,RMVar_hsa_circ_41430,RMVar_hsa_circ_161989,RMVar_hsa_circ_161990,RMVar_hsa_circ_43851,RMVar_hsa_circ_273271,RMVar_hsa_circ_346778,RMVar_hsa_circ_95623,RMVar_hsa_circ_161991 21018 RMVar_ID_21018 Human_SNP_ID_522876816 A-to-I Human chr13 + 20061804 20061804 20061804 AGAGACAGGGCTTCCCTATGTTGGCCAGGCTGATCTCAAACTCCTGACCTCAGGTGATCCACCTG AGAGACAGGGCTTCCCTATGTTGGCCAGGCTGTTCTCAAACTCCTGACCTCAGGTGATCCACCTG A T ZMYM2 Ensembl:ENSG00000121741 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1397085532 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_309496,RMVar_hsa_circ_161989,RMVar_hsa_circ_95623,RMVar_hsa_circ_161991,RMVar_hsa_circ_20610,RMVar_hsa_circ_35780,RMVar_hsa_circ_47766,RMVar_hsa_circ_162001,RMVar_hsa_circ_161996,RMVar_hsa_circ_342333,RMVar_hsa_circ_7117,RMVar_hsa_circ_49760,RMVar_hsa_circ_162008,RMVar_hsa_circ_33002,RMVar_hsa_circ_308199,RMVar_hsa_circ_311930,RMVar_hsa_circ_346297,RMVar_hsa_circ_47612,RMVar_hsa_circ_162006,RMVar_hsa_circ_162007,RMVar_hsa_circ_301929,RMVar_hsa_circ_162015,RMVar_hsa_circ_162020,RMVar_hsa_circ_162016,RMVar_hsa_circ_334338,RMVar_hsa_circ_378927,RMVar_hsa_circ_354531,RMVar_hsa_circ_272591,RMVar_hsa_circ_29217,RMVar_hsa_circ_162018,RMVar_hsa_circ_22275,RMVar_hsa_circ_303511,RMVar_hsa_circ_316050,RMVar_hsa_circ_323881,RMVar_hsa_circ_326455,RMVar_hsa_circ_273100,RMVar_hsa_circ_300738,RMVar_hsa_circ_162021,RMVar_hsa_circ_9548,RMVar_hsa_circ_19140,RMVar_hsa_circ_162019,RMVar_hsa_circ_322758,RMVar_hsa_circ_331379,RMVar_hsa_circ_162026,RMVar_hsa_circ_24471,RMVar_hsa_circ_317671,RMVar_hsa_circ_364873,RMVar_hsa_circ_279632,RMVar_hsa_circ_14857,RMVar_hsa_circ_162027,RMVar_hsa_circ_162028,RMVar_hsa_circ_162029 21019 RMVar_ID_21019 Human_SNP_ID_522880222 A-to-I Human chr13 + 20074570 20074570 20074570 CCTTCCTTTTTTTTTTTTTGAGACGGAGTCTTACTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCG CCTTCCTTTTTTTTTTTTTGAGACGGAGTCTTGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCG A G ZMYM2 Ensembl:ENSG00000121741 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1165216511 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_117929 RMVar_hsa_circ_162030,RMVar_hsa_circ_378927,RMVar_hsa_circ_354531,RMVar_hsa_circ_323881,RMVar_hsa_circ_300738,RMVar_hsa_circ_162019,RMVar_hsa_circ_322758,RMVar_hsa_circ_317671,RMVar_hsa_circ_364873,RMVar_hsa_circ_162029,RMVar_hsa_circ_297133,RMVar_hsa_circ_162036,RMVar_hsa_circ_162035,RMVar_hsa_circ_280928,RMVar_hsa_circ_272905,RMVar_hsa_circ_162034,RMVar_hsa_circ_289652,RMVar_hsa_circ_308474,RMVar_hsa_circ_162037 21020 RMVar_ID_21020 Human_SNP_ID_523013787 A-to-I Human chr13 + 20592670 20592670 20592670 TTTTGTATTTTTGGTAGAGATGGGGTTTTGCCATGCTGGCTAGGCTGGTCTCGAACTCCCAATCT TTTTGTATTTTTGGTAGAGATGGGGTTTTGCCGTGCTGGCTAGGCTGGTCTCGAACTCCCAATCT A G IFT88 Ensembl:ENSG00000032742 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs781620353 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40344,RMVar_hsa_circ_316730,RMVar_hsa_circ_13767,RMVar_hsa_circ_60668,RMVar_hsa_circ_343546,RMVar_hsa_circ_358217,RMVar_hsa_circ_43544,RMVar_hsa_circ_36372,RMVar_hsa_circ_53075,RMVar_hsa_circ_322394,RMVar_hsa_circ_338790,RMVar_hsa_circ_351984,RMVar_hsa_circ_338373,RMVar_hsa_circ_305597,RMVar_hsa_circ_292035,RMVar_hsa_circ_65290,RMVar_hsa_circ_75045,RMVar_hsa_circ_59435,RMVar_hsa_circ_162051,RMVar_hsa_circ_162052,RMVar_hsa_circ_162053,RMVar_hsa_circ_162050,RMVar_hsa_circ_275262,RMVar_hsa_circ_349536,RMVar_hsa_circ_54325,RMVar_hsa_circ_41685,RMVar_hsa_circ_71796,RMVar_hsa_circ_162054,RMVar_hsa_circ_162055,RMVar_hsa_circ_74447,RMVar_hsa_circ_59351,RMVar_hsa_circ_67871,RMVar_hsa_circ_350509,RMVar_hsa_circ_353711,RMVar_hsa_circ_359104,RMVar_hsa_circ_71610,RMVar_hsa_circ_66131,RMVar_hsa_circ_162057 21021 RMVar_ID_21021 Human_SNP_ID_523013788 A-to-I Human chr13 + 20592670 20592670 20592670 TTTTGTATTTTTGGTAGAGATGGGGTTTTGCCATGCTGGCTAGGCTGGTCTCGAACTCCCAATCT TTTTGTATTTTTGGTAGAGATGGGGTTTTGCCTTGCTGGCTAGGCTGGTCTCGAACTCCCAATCT A T IFT88 Ensembl:ENSG00000032742 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs781620353 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40344,RMVar_hsa_circ_316730,RMVar_hsa_circ_13767,RMVar_hsa_circ_60668,RMVar_hsa_circ_343546,RMVar_hsa_circ_358217,RMVar_hsa_circ_43544,RMVar_hsa_circ_36372,RMVar_hsa_circ_53075,RMVar_hsa_circ_322394,RMVar_hsa_circ_338790,RMVar_hsa_circ_351984,RMVar_hsa_circ_338373,RMVar_hsa_circ_305597,RMVar_hsa_circ_292035,RMVar_hsa_circ_65290,RMVar_hsa_circ_75045,RMVar_hsa_circ_59435,RMVar_hsa_circ_162051,RMVar_hsa_circ_162052,RMVar_hsa_circ_162053,RMVar_hsa_circ_162050,RMVar_hsa_circ_275262,RMVar_hsa_circ_349536,RMVar_hsa_circ_54325,RMVar_hsa_circ_41685,RMVar_hsa_circ_71796,RMVar_hsa_circ_162054,RMVar_hsa_circ_162055,RMVar_hsa_circ_74447,RMVar_hsa_circ_59351,RMVar_hsa_circ_67871,RMVar_hsa_circ_350509,RMVar_hsa_circ_353711,RMVar_hsa_circ_359104,RMVar_hsa_circ_71610,RMVar_hsa_circ_66131,RMVar_hsa_circ_162057 21022 RMVar_ID_21022 Human_SNP_ID_523014074 A-to-I Human chr13 + 20593848 20593848 20593848 AAGGTGAGAGGATCACTTGAGCCCAGGAGTTCAAGACTAGCCTGGGCAACATAGCGAGACCCCGT AAGGTGAGAGGATCACTTGAGCCCAGGAGTTCCAGACTAGCCTGGGCAACATAGCGAGACCCCGT A C IFT88 Ensembl:ENSG00000032742 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1195744657 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40344,RMVar_hsa_circ_316730,RMVar_hsa_circ_13767,RMVar_hsa_circ_60668,RMVar_hsa_circ_343546,RMVar_hsa_circ_358217,RMVar_hsa_circ_43544,RMVar_hsa_circ_36372,RMVar_hsa_circ_53075,RMVar_hsa_circ_322394,RMVar_hsa_circ_338790,RMVar_hsa_circ_351984,RMVar_hsa_circ_338373,RMVar_hsa_circ_305597,RMVar_hsa_circ_292035,RMVar_hsa_circ_65290,RMVar_hsa_circ_75045,RMVar_hsa_circ_59435,RMVar_hsa_circ_162051,RMVar_hsa_circ_162052,RMVar_hsa_circ_162053,RMVar_hsa_circ_162050,RMVar_hsa_circ_275262,RMVar_hsa_circ_349536,RMVar_hsa_circ_54325,RMVar_hsa_circ_41685,RMVar_hsa_circ_71796,RMVar_hsa_circ_162054,RMVar_hsa_circ_162055,RMVar_hsa_circ_74447,RMVar_hsa_circ_59351,RMVar_hsa_circ_67871,RMVar_hsa_circ_350509,RMVar_hsa_circ_353711,RMVar_hsa_circ_359104,RMVar_hsa_circ_71610,RMVar_hsa_circ_66131,RMVar_hsa_circ_162057 21023 RMVar_ID_21023 Human_SNP_ID_523029232 A-to-I Human chr13 + 20655276 20655276 20655276 CAACATGGTGAAACCCCATCTCTACTAATAATACAAAAATTAGCTGGGCTTGGTGGTGCACGCCT CAACATGGTGAAACCCCATCTCTACTAATAATGCAAAAATTAGCTGGGCTTGGTGGTGCACGCCT A G IFT88 Ensembl:ENSG00000032742 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1380142127 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6964,RMVar_hsa_circ_40344,RMVar_hsa_circ_43544,RMVar_hsa_circ_322394,RMVar_hsa_circ_162053,RMVar_hsa_circ_74447,RMVar_hsa_circ_353711,RMVar_hsa_circ_162057,RMVar_hsa_circ_70027,RMVar_hsa_circ_351135,RMVar_hsa_circ_355350,RMVar_hsa_circ_349717,RMVar_hsa_circ_363029,RMVar_hsa_circ_162075,RMVar_hsa_circ_294968,RMVar_hsa_circ_162070,RMVar_hsa_circ_325347,RMVar_hsa_circ_6641,RMVar_hsa_circ_162073,RMVar_hsa_circ_13811,RMVar_hsa_circ_162074,RMVar_hsa_circ_346599,RMVar_hsa_circ_282658,RMVar_hsa_circ_371064,RMVar_hsa_circ_162076 21024 RMVar_ID_21024 Human_SNP_ID_523029233 A-to-I Human chr13 + 20655279 20655279 20655279 CATGGTGAAACCCCATCTCTACTAATAATACAAAAATTAGCTGGGCTTGGTGGTGCACGCCTGTA CATGGTGAAACCCCATCTCTACTAATAATACAGAAATTAGCTGGGCTTGGTGGTGCACGCCTGTA A G IFT88 Ensembl:ENSG00000032742 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs752789297 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6964,RMVar_hsa_circ_40344,RMVar_hsa_circ_43544,RMVar_hsa_circ_322394,RMVar_hsa_circ_162053,RMVar_hsa_circ_74447,RMVar_hsa_circ_353711,RMVar_hsa_circ_162057,RMVar_hsa_circ_70027,RMVar_hsa_circ_351135,RMVar_hsa_circ_355350,RMVar_hsa_circ_349717,RMVar_hsa_circ_363029,RMVar_hsa_circ_162075,RMVar_hsa_circ_294968,RMVar_hsa_circ_162070,RMVar_hsa_circ_325347,RMVar_hsa_circ_6641,RMVar_hsa_circ_162073,RMVar_hsa_circ_13811,RMVar_hsa_circ_162074,RMVar_hsa_circ_346599,RMVar_hsa_circ_282658,RMVar_hsa_circ_371064,RMVar_hsa_circ_162076 21025 RMVar_ID_21025 Human_SNP_ID_523029648 A-to-I Human chr13 + 20656945 20656945 20656945 CAGTGGTGTGATCTCAGCTCACCACAACCTCCACCTCCTGAGTTCAAGTGATTCTCCTGCCTCAG CAGTGGTGTGATCTCAGCTCACCACAACCTCCTCCTCCTGAGTTCAAGTGATTCTCCTGCCTCAG A T IFT88 Ensembl:ENSG00000032742 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1363572784 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40344,RMVar_hsa_circ_74447,RMVar_hsa_circ_353711,RMVar_hsa_circ_162057,RMVar_hsa_circ_349717,RMVar_hsa_circ_363029,RMVar_hsa_circ_162070,RMVar_hsa_circ_325347,RMVar_hsa_circ_6641,RMVar_hsa_circ_13811,RMVar_hsa_circ_282658,RMVar_hsa_circ_162076,RMVar_hsa_circ_162077 21026 RMVar_ID_21026 Human_SNP_ID_523041974 A-to-I Human chr13 + 20707614 20707614 20707614 ACACAGACAGATCAATGCAGCCTTGACCTTCTAGGCTCAAGGGATCCTCCTACCTCAGCCTCCCA ACACAGACAGATCAATGCAGCCTTGACCTTCTCGGCTCAAGGGATCCTCCTACCTCAGCCTCCCA A C IL17D Ensembl:ENSG00000172458 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs575154162 Functional Loss SNV dbSNP153 33..33 33 - - - 21027 RMVar_ID_21027 Human_SNP_ID_523041975 A-to-I Human chr13 + 20707614 20707614 20707614 ACACAGACAGATCAATGCAGCCTTGACCTTCTAGGCTCAAGGGATCCTCCTACCTCAGCCTCCCA ACACAGACAGATCAATGCAGCCTTGACCTTCTGGGCTCAAGGGATCCTCCTACCTCAGCCTCCCA A G IL17D Ensembl:ENSG00000172458 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs575154162 Functional Loss SNV dbSNP153 33..33 33 - - - 21028 RMVar_ID_21028 Human_SNP_ID_523060078 A-to-I Human chr13 + 20775864 20775864 20775864 TGAGACCAGCCTGGTCAACATGGCGGAACTCCATCTCTACTAAAAATACAAAAATTAGCCCGGTG TGAGACCAGCCTGGTCAACATGGCGGAACTCCCTCTCTACTAAAAATACAAAAATTAGCCCGGTG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs972168919 Functional Loss SNV dbSNP153 33..33 33 - - - 21029 RMVar_ID_21029 Human_SNP_ID_523113241 A-to-I Human chr13 - 20982835 20982835 20982835 AGTCACGCACCACCACCTCTGGCTAATTTTGTATTTTTAGTAGAGACGGGGTTTCTCCGTGTTGG AGTCACGCACCACCACCTCTGGCTAATTTTGTGTTTTTAGTAGAGACGGGGTTTCTCCGTGTTGG T C LATS2 Ensembl:ENSG00000150457 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1394495058 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111205,RMVar_hsa_circ_123728,RMVar_hsa_circ_162132,RMVar_hsa_circ_330919,RMVar_hsa_circ_162133,RMVar_hsa_circ_369704,RMVar_hsa_circ_162135,RMVar_hsa_circ_106323,RMVar_hsa_circ_162136,RMVar_hsa_circ_162137 21030 RMVar_ID_21030 Human_SNP_ID_523120794 A-to-I Human chr13 - 21007939 21007939 21007939 GCCTGGACAACATGGCAAACCCTGTCTCTACTAAAAATACAAAAATTAGTCGGTTGTGATGATTC GCCTGGACAACATGGCAAACCCTGTCTCTACTCAAAATACAAAAATTAGTCGGTTGTGATGATTC T G LATS2 Ensembl:ENSG00000150457 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1357028346 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111205,RMVar_hsa_circ_123728,RMVar_hsa_circ_162132,RMVar_hsa_circ_162137,RMVar_hsa_circ_89270,RMVar_hsa_circ_162139 21031 RMVar_ID_21031 Human_SNP_ID_523123978 A-to-I Human chr13 - 21020940 21020940 21020940 CCTTCCCAACCACGGATGTGTGGCTTAAAGATAATAAAGTGAATTTGGAGAGAAGAGAAGGCTAA CCTTCCCAACCACGGATGTGTGGCTTAAAGATGATAAAGTGAATTTGGAGAGAAGAGAAGGCTAA T C LATS2 Ensembl:ENSG00000150457 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs911962685 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111205,RMVar_hsa_circ_123728,RMVar_hsa_circ_162132,RMVar_hsa_circ_162137,RMVar_hsa_circ_89270,RMVar_hsa_circ_162139 21032 RMVar_ID_21032 Human_SNP_ID_523124194 A-to-I Human chr13 - 21021745 21021745 21021745 TTCACAACAGACTGGACCAAGGGCATGCTCTTAGCCTCGCTGTTCTCTGCAGATTCACTTCATTA TTCACAACAGACTGGACCAAGGGCATGCTCTTGGCCTCGCTGTTCTCTGCAGATTCACTTCATTA T C LATS2 Ensembl:ENSG00000150457 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs541200167 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111205,RMVar_hsa_circ_123728,RMVar_hsa_circ_162132,RMVar_hsa_circ_162137,RMVar_hsa_circ_89270,RMVar_hsa_circ_162139 21033 RMVar_ID_21033 Human_SNP_ID_523126276 A-to-I Human chr13 - 21029530 21029530 21029530 CCTTGGCCTCCCAAAGTCCTGGGATTACAGGCATGAGCCACCGCACCCGACATTCCAATATCTTT CCTTGGCCTCCCAAAGTCCTGGGATTACAGGCGTGAGCCACCGCACCCGACATTCCAATATCTTT T C LATS2 Ensembl:ENSG00000150457 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1191585223 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111205,RMVar_hsa_circ_123728,RMVar_hsa_circ_162132,RMVar_hsa_circ_162137,RMVar_hsa_circ_89270,RMVar_hsa_circ_162139 21034 RMVar_ID_21034 Human_SNP_ID_523126278 A-to-I Human chr13 - 21029536 21029536 21029536 CGCCTGCCTTGGCCTCCCAAAGTCCTGGGATTACAGGCATGAGCCACCGCACCCGACATTCCAAT CGCCTGCCTTGGCCTCCCAAAGTCCTGGGATTGCAGGCATGAGCCACCGCACCCGACATTCCAAT T C LATS2 Ensembl:ENSG00000150457 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs536775730 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111205,RMVar_hsa_circ_123728,RMVar_hsa_circ_162132,RMVar_hsa_circ_162137,RMVar_hsa_circ_89270,RMVar_hsa_circ_162139 21035 RMVar_ID_21035 Human_SNP_ID_523155284 A-to-I Human chr13 + 21141766 21141766 21141766 TCGGCTCACTGCAACCTCCACCTCCTGGATTCAATTGATTCTTCTGACTCAGCCTCCCAAGTAGC TCGGCTCACTGCAACCTCCACCTCCTGGATTCGATTGATTCTTCTGACTCAGCCTCCCAAGTAGC A G SAP18 Ensembl:ENSG00000150459 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1194897307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8389231 21036 RMVar_ID_21036 Human_SNP_ID_523155308 A-to-I Human chr13 + 21141847 21141847 21141847 CACCACCACGCCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCGTATTGACCAGGC CACCACCACGCCTGGCTAATTTTTGTATTTTTGGTAGAGATGGGGTTTCACCGTATTGACCAGGC A G SAP18 Ensembl:ENSG00000150459 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1390173586 Functional Loss SNV dbSNP153 33..33 33 - - - 21037 RMVar_ID_21037 Human_SNP_ID_523155309 A-to-I Human chr13 + 21141850 21141849 21141850 CACCACGCCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCGTATTGACCAGGCTGG CACCACGCCTGGCTAATTTTTGTATTTTTAGT_GAGATGGGGTTTCACCGTATTGACCAGGCTGG TA T SAP18 Ensembl:ENSG00000150459 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1403145502 Functional Loss DEL dbSNP153 33..33 33 - - - 21038 RMVar_ID_21038 Human_SNP_ID_523156337 A-to-I Human chr13 + 21145693 21145693 21145693 TGCCACAACGCCTGGCTAATTTTTGGATTTTTAGTAGAAACGGGGTTTCACCATGTTGGCCAGGC TGCCACAACGCCTGGCTAATTTTTGGATTTTTCGTAGAAACGGGGTTTCACCATGTTGGCCAGGC A C SAP18 Ensembl:ENSG00000150459 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1045865348 Functional Loss SNV dbSNP153 33..33 33 - - - 21039 RMVar_ID_21039 Human_SNP_ID_523156338 A-to-I Human chr13 + 21145693 21145693 21145693 TGCCACAACGCCTGGCTAATTTTTGGATTTTTAGTAGAAACGGGGTTTCACCATGTTGGCCAGGC TGCCACAACGCCTGGCTAATTTTTGGATTTTTGGTAGAAACGGGGTTTCACCATGTTGGCCAGGC A G SAP18 Ensembl:ENSG00000150459 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1045865348 Functional Loss SNV dbSNP153 33..33 33 - - - 21040 RMVar_ID_21040 Human_SNP_ID_523156487 A-to-I Human chr13 + 21146185 21146185 21146185 CATGGCCAACATGGTGAAACCCTGTCTCTACTAAAAATAGAAAAATTACCTGGGCGTGGTGGTGG CATGGCCAACATGGTGAAACCCTGTCTCTACTGAAAATAGAAAAATTACCTGGGCGTGGTGGTGG A G SAP18 Ensembl:ENSG00000150459 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs766050248 Functional Loss SNV dbSNP153 33..33 33 - - - 21041 RMVar_ID_21041 Human_SNP_ID_523160949 A-to-I Human chr13 - 21163014 21163014 21163014 TCTTTCCATGAAACATTCCCACCACCCAGGCTAGAGTGCAGTGGCAGGATGATAGCTCACTGCAG TCTTTCCATGAAACATTCCCACCACCCAGGCTGGAGTGCAGTGGCAGGATGATAGCTCACTGCAG T C SKA3 Ensembl:ENSG00000165480 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs868445703 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_371729,RMVar_hsa_circ_265832,RMVar_hsa_circ_162141,RMVar_hsa_circ_289076,RMVar_hsa_circ_162145,RMVar_hsa_circ_21676,RMVar_hsa_circ_302733,RMVar_hsa_circ_162144,RMVar_hsa_circ_287050,RMVar_hsa_circ_336516,RMVar_hsa_circ_162146 21042 RMVar_ID_21042 Human_SNP_ID_523161157 A-to-I Human chr13 - 21163856 21163856 21163856 GTTAGGCTCATAGAGAAGAATTGTTTGAACCCAGGAGATGGAGGTTGCAGTGAGCTGAGATCGTG GTTAGGCTCATAGAGAAGAATTGTTTGAACCCCGGAGATGGAGGTTGCAGTGAGCTGAGATCGTG T G SKA3 Ensembl:ENSG00000165480 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037664294 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12114836 RMVar_hsa_circ_371729,RMVar_hsa_circ_265832,RMVar_hsa_circ_162141,RMVar_hsa_circ_289076,RMVar_hsa_circ_162145,RMVar_hsa_circ_21676,RMVar_hsa_circ_302733,RMVar_hsa_circ_162144,RMVar_hsa_circ_287050,RMVar_hsa_circ_336516,RMVar_hsa_circ_162146 21043 RMVar_ID_21043 Human_SNP_ID_523213396 A-to-I Human chr13 - 21374353 21374353 21374353 AGGCATGGTGGCACACGCCTGTAGTCCCAACTACTCGGGAGGTGGAGGCAGGAGAATCACTTGAA AGGCATGGTGGCACACGCCTGTAGTCCCAACTGCTCGGGAGGTGGAGGCAGGAGAATCACTTGAA T C ZDHHC20 Ensembl:ENSG00000180776 Protein coding 3'UTR GSE47997;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829 K562 cells&HepG2 cells;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line - 23474544,29796672,31158229 RNA-Seq:(High) rs1391495444 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_118323,Human_RBP_ID_4265531,Human_RBP_ID_23306400,Human_RBP_ID_26424825 RMVar_hsa_circ_82999,RMVar_hsa_circ_104322,RMVar_hsa_circ_112681,RMVar_hsa_circ_88460,RMVar_hsa_circ_162151,RMVar_hsa_circ_162153,RMVar_hsa_circ_162154,RMVar_hsa_circ_162152 21044 RMVar_ID_21044 Human_SNP_ID_523213397 A-to-I Human chr13 - 21374356 21374356 21374356 TCCAGGCATGGTGGCACACGCCTGTAGTCCCAACTACTCGGGAGGTGGAGGCAGGAGAATCACTT TCCAGGCATGGTGGCACACGCCTGTAGTCCCAGCTACTCGGGAGGTGGAGGCAGGAGAATCACTT T C ZDHHC20 Ensembl:ENSG00000180776 Protein coding 3'UTR GSE47997;GSE38233;GSE112787;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;293 Flip-In T-REx cells,empty vector;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,29967493,31158229,31158229,32596459 RNA-Seq:(High) rs1282877635 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_118323,Human_RBP_ID_23306400,Human_RBP_ID_26424825 RMVar_hsa_circ_82999,RMVar_hsa_circ_104322,RMVar_hsa_circ_112681,RMVar_hsa_circ_88460,RMVar_hsa_circ_162151,RMVar_hsa_circ_162153,RMVar_hsa_circ_162154,RMVar_hsa_circ_162152 21045 RMVar_ID_21045 Human_SNP_ID_523213398 A-to-I Human chr13 - 21374363 21374363 21374363 AAAACTGTCCAGGCATGGTGGCACACGCCTGTAGTCCCAACTACTCGGGAGGTGGAGGCAGGAGA AAAACTGTCCAGGCATGGTGGCACACGCCTGTGGTCCCAACTACTCGGGAGGTGGAGGCAGGAGA T C ZDHHC20 Ensembl:ENSG00000180776 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line - 23474544,24183664,29129909,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs748880972 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_118323,Human_RBP_ID_17359167,Human_RBP_ID_23159647,Human_RBP_ID_23306400,Human_RBP_ID_26424826 RMVar_hsa_circ_82999,RMVar_hsa_circ_104322,RMVar_hsa_circ_112681,RMVar_hsa_circ_88460,RMVar_hsa_circ_162151,RMVar_hsa_circ_162153,RMVar_hsa_circ_162154,RMVar_hsa_circ_162152 21046 RMVar_ID_21046 Human_SNP_ID_523213451 A-to-I Human chr13 - 21374486 21374486 21374486 TCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCTGGCGGATCACCTGAGGTCAGGGGTTCG TCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCTGGCGGATCACCTGAGGTCAGGGGTTCG T C ZDHHC20 Ensembl:ENSG00000180776 Protein coding 3'UTR GSE38233;GSE112787;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;293 Flip-In T-REx cells,empty vector;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29967493,32596459 RNA-Seq:(High) rs1411282817 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82999,RMVar_hsa_circ_104322,RMVar_hsa_circ_112681,RMVar_hsa_circ_88460,RMVar_hsa_circ_162151,RMVar_hsa_circ_162153,RMVar_hsa_circ_162154,RMVar_hsa_circ_162152 21047 RMVar_ID_21047 Human_SNP_ID_523213556 A-to-I Human chr13 - 21374889 21374888 21374889 CCTCAAATAATCCACCCACCTCAGCTTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCACGCC CCTCAAATAATCCACCCACCTCAGCTTCCCAA_GTGCTGGGATTACAGGCGTGAGCCACCACGCC CT C ZDHHC20 Ensembl:ENSG00000180776 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,31158229,31158229,32596459 RNA-Seq:(High) rs779430398 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_82999,RMVar_hsa_circ_104322,RMVar_hsa_circ_112681,RMVar_hsa_circ_88460,RMVar_hsa_circ_162151,RMVar_hsa_circ_162153,RMVar_hsa_circ_162154,RMVar_hsa_circ_162152 21048 RMVar_ID_21048 Human_SNP_ID_523213566 A-to-I Human chr13 - 21374942 21374942 21374942 TTTAGAAGAGACGAGGTTTCACCATGTTGACCAGGCTGATCACTAACTCCTGACCTCAAATAATC TTTAGAAGAGACGAGGTTTCACCATGTTGACCGGGCTGATCACTAACTCCTGACCTCAAATAATC T C ZDHHC20 Ensembl:ENSG00000180776 Protein coding 3'UTR GSE100210;GSE107867 HepG2 cell line;ASD brains,frontal_cortex - 29129909,30559470 RNA-Seq:(High) rs1258420544 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82999,RMVar_hsa_circ_104322,RMVar_hsa_circ_112681,RMVar_hsa_circ_88460,RMVar_hsa_circ_162151,RMVar_hsa_circ_162153,RMVar_hsa_circ_162154,RMVar_hsa_circ_162152 21049 RMVar_ID_21049 Human_SNP_ID_523213571 A-to-I Human chr13 - 21374954 21374954 21374954 AATTTTCACATTTTTAGAAGAGACGAGGTTTCACCATGTTGACCAGGCTGATCACTAACTCCTGA AATTTTCACATTTTTAGAAGAGACGAGGTTTCGCCATGTTGACCAGGCTGATCACTAACTCCTGA T C ZDHHC20 Ensembl:ENSG00000180776 Protein coding 3'UTR GSE38233;GSE112787;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;293 Flip-In T-REx cells,empty vector;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29967493,31158229,32596459,32596459 RNA-Seq:(High) rs755582559 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4277982 Human_miRNA_ID_2761963 RMVar_hsa_circ_82999,RMVar_hsa_circ_104322,RMVar_hsa_circ_112681,RMVar_hsa_circ_88460,RMVar_hsa_circ_162151,RMVar_hsa_circ_162153,RMVar_hsa_circ_162154,RMVar_hsa_circ_162152 21050 RMVar_ID_21050 Human_SNP_ID_523213576 A-to-I Human chr13 - 21374968 21374968 21374968 CACCATGCCCGGCTAATTTTCACATTTTTAGAAGAGACGAGGTTTCACCATGTTGACCAGGCTGA CACCATGCCCGGCTAATTTTCACATTTTTAGAGGAGACGAGGTTTCACCATGTTGACCAGGCTGA T C ZDHHC20 Ensembl:ENSG00000180776 Protein coding 3'UTR GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,29796672,31158229,31158229,31158229,32596459,32596459 RNA-Seq:(High) rs1391140170 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26426799 RMVar_hsa_circ_82999,RMVar_hsa_circ_104322,RMVar_hsa_circ_112681,RMVar_hsa_circ_88460,RMVar_hsa_circ_162151,RMVar_hsa_circ_162153,RMVar_hsa_circ_162154,RMVar_hsa_circ_162152 21051 RMVar_ID_21051 Human_SNP_ID_523213603 A-to-I Human chr13 - 21375026 21375026 21375026 AGGTTCAATAGAGTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCTCATGCCACCATG AGGTTCAATAGAGTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCTCATGCCACCATG T C ZDHHC20 Ensembl:ENSG00000180776 Protein coding 3'UTR GSE47997;GSE100210;GSE112787;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;HepG2 cell line;293 Flip-In T-REx cells,empty vector;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,29129909,29967493,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs1466649094 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82999,RMVar_hsa_circ_104322,RMVar_hsa_circ_112681,RMVar_hsa_circ_88460,RMVar_hsa_circ_162151,RMVar_hsa_circ_162153,RMVar_hsa_circ_162154,RMVar_hsa_circ_162152 21052 RMVar_ID_21052 Human_SNP_ID_523215331 A-to-I Human chr13 - 21380782 21380782 21380782 CAACGTTATTCTTTTTTTTTTTTTGAGATGGAATTTCGCTCTGTCACCAGGCTAGAGTGCAGTGG CAACGTTATTCTTTTTTTTTTTTTGAGATGGATTTTCGCTCTGTCACCAGGCTAGAGTGCAGTGG T A ZDHHC20 Ensembl:ENSG00000180776 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs546359327 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82999,RMVar_hsa_circ_112681,RMVar_hsa_circ_88460,RMVar_hsa_circ_162151,RMVar_hsa_circ_162153,RMVar_hsa_circ_162152,RMVar_hsa_circ_287176 21053 RMVar_ID_21053 Human_SNP_ID_523215332 A-to-I Human chr13 - 21380782 21380782 21380782 CAACGTTATTCTTTTTTTTTTTTTGAGATGGAATTTCGCTCTGTCACCAGGCTAGAGTGCAGTGG CAACGTTATTCTTTTTTTTTTTTTGAGATGGAGTTTCGCTCTGTCACCAGGCTAGAGTGCAGTGG T C ZDHHC20 Ensembl:ENSG00000180776 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs546359327 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82999,RMVar_hsa_circ_112681,RMVar_hsa_circ_88460,RMVar_hsa_circ_162151,RMVar_hsa_circ_162153,RMVar_hsa_circ_162152,RMVar_hsa_circ_287176 21054 RMVar_ID_21054 Human_SNP_ID_523215541 A-to-I Human chr13 - 21381466 21381461 21381466 CCGCTTGTTGGACAGTGAATCTCAGTGGCTGGAGAATGGAGCTGAAGAAGGCATCGTCAAATCAG CCGCTTGTTGGACAGTGAATCTCAGTGGCTGG_____GGAGCTGAAGAAGGCATCGTCAAATCAG CATTCT C ZDHHC20 Ensembl:ENSG00000180776 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs867184638 Functional Loss DEL dbSNP153 33..37 33 - - - Human_RBP_ID_3944209,Human_RBP_ID_8788694,Human_RBP_ID_12115083,Human_RBP_ID_23588441,Human_RBP_ID_27807587 Human_Splice_Rec_1450144,Human_Splice_Rec_1450145,Human_Splice_Rec_1450164,Human_Splice_Rec_1450165,Human_Splice_Rec_1450167,Human_Splice_Rec_1450190,Human_Splice_Rec_1450191,Human_Splice_Rec_1450198,Human_Splice_Rec_1450199,Human_Splice_Rec_1450222,Human_Splice_Rec_1450223,Human_Splice_Rec_1450232,Human_Splice_Rec_1450233,Human_Splice_Rec_1450250,Human_Splice_Rec_1450251,Human_Splice_Rec_1450272,Human_Splice_Rec_1450273,Human_Splice_Rec_1450276 Human_miRNA_ID_2047854,Human_miRNA_ID_2974163,Human_miRNA_ID_3007352 RMVar_hsa_circ_162155,RMVar_hsa_circ_82999,RMVar_hsa_circ_112681,RMVar_hsa_circ_88460,RMVar_hsa_circ_286141,RMVar_hsa_circ_307748,RMVar_hsa_circ_162151,RMVar_hsa_circ_162153,RMVar_hsa_circ_162152,RMVar_hsa_circ_325405,RMVar_hsa_circ_287176,RMVar_hsa_circ_356545,RMVar_hsa_circ_314427,RMVar_hsa_circ_305715,RMVar_hsa_circ_306842,RMVar_hsa_circ_288579,RMVar_hsa_circ_162159,RMVar_hsa_circ_270009,RMVar_hsa_circ_279831,RMVar_hsa_circ_162160,RMVar_hsa_circ_162157,RMVar_hsa_circ_162158,RMVar_hsa_circ_162156 21055 RMVar_ID_21055 Human_SNP_ID_523215545 A-to-I Human chr13 - 21381466 21381466 21381466 CCGCTTGTTGGACAGTGAATCTCAGTGGCTGGAGAATGGAGCTGAAGAAGGCATCGTCAAATCAG CCGCTTGTTGGACAGTGAATCTCAGTGGCTGGGGAATGGAGCTGAAGAAGGCATCGTCAAATCAG T C ZDHHC20 Ensembl:ENSG00000180776 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs757596481 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3944209,Human_RBP_ID_8788694,Human_RBP_ID_12115083,Human_RBP_ID_23588441,Human_RBP_ID_27807587 Human_Splice_Rec_1450144,Human_Splice_Rec_1450145,Human_Splice_Rec_1450164,Human_Splice_Rec_1450165,Human_Splice_Rec_1450167,Human_Splice_Rec_1450190,Human_Splice_Rec_1450191,Human_Splice_Rec_1450198,Human_Splice_Rec_1450199,Human_Splice_Rec_1450222,Human_Splice_Rec_1450223,Human_Splice_Rec_1450232,Human_Splice_Rec_1450233,Human_Splice_Rec_1450250,Human_Splice_Rec_1450251,Human_Splice_Rec_1450272,Human_Splice_Rec_1450273,Human_Splice_Rec_1450276 Human_miRNA_ID_2047854,Human_miRNA_ID_2974163,Human_miRNA_ID_3007352 RMVar_hsa_circ_162155,RMVar_hsa_circ_82999,RMVar_hsa_circ_112681,RMVar_hsa_circ_88460,RMVar_hsa_circ_286141,RMVar_hsa_circ_307748,RMVar_hsa_circ_162151,RMVar_hsa_circ_162153,RMVar_hsa_circ_162152,RMVar_hsa_circ_325405,RMVar_hsa_circ_287176,RMVar_hsa_circ_356545,RMVar_hsa_circ_314427,RMVar_hsa_circ_305715,RMVar_hsa_circ_306842,RMVar_hsa_circ_288579,RMVar_hsa_circ_162159,RMVar_hsa_circ_270009,RMVar_hsa_circ_279831,RMVar_hsa_circ_162160,RMVar_hsa_circ_162157,RMVar_hsa_circ_162158,RMVar_hsa_circ_162156 21056 RMVar_ID_21056 Human_SNP_ID_523244404 A-to-I Human chr13 - 21496582 21496582 21496582 AGAACCGGAATTTCAGCATTAAAAGTCCATCTAACTCCAAAACTCTGTGCTCTTACTCAGTGCTA AGAACCGGAATTTCAGCATTAAAAGTCCATCTGACTCCAAAACTCTGTGCTCTTACTCAGTGCTA T C MICU2 Ensembl:ENSG00000165487 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1034752992 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_162177,RMVar_hsa_circ_103999,RMVar_hsa_circ_162179,RMVar_hsa_circ_162178 21057 RMVar_ID_21057 Human_SNP_ID_523244464 A-to-I Human chr13 - 21496799 21496799 21496799 CGCCCGCCTCCGCCTCCCAAAGTGCTGGGATTACAGGCGTCAGTCACCGCGCCCGCACCATTTGT CGCCCGCCTCCGCCTCCCAAAGTGCTGGGATTGCAGGCGTCAGTCACCGCGCCCGCACCATTTGT T C MICU2 Ensembl:ENSG00000165487 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1236889891 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_162177,RMVar_hsa_circ_103999,RMVar_hsa_circ_162179,RMVar_hsa_circ_162178 21058 RMVar_ID_21058 Human_SNP_ID_523244740 A-to-I Human chr13 - 21497887 21497887 21497887 AACATTAGTTGGGTGTGGTGCTCTGTGTCTGTAGTCCCAGCTACTTGGGAGACTGAGGCAGGAGG AACATTAGTTGGGTGTGGTGCTCTGTGTCTGTGGTCCCAGCTACTTGGGAGACTGAGGCAGGAGG T C MICU2 Ensembl:ENSG00000165487 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1436909433 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_162177,RMVar_hsa_circ_103999,RMVar_hsa_circ_162179,RMVar_hsa_circ_162178 21059 RMVar_ID_21059 Human_SNP_ID_523244745 A-to-I Human chr13 - 21497913 21497913 21497913 TCGTCTCTACTAAAAACAGAAATAAAAACATTAGTTGGGTGTGGTGCTCTGTGTCTGTAGTCCCA TCGTCTCTACTAAAAACAGAAATAAAAACATTTGTTGGGTGTGGTGCTCTGTGTCTGTAGTCCCA T A MICU2 Ensembl:ENSG00000165487 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1178613955 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_162177,RMVar_hsa_circ_103999,RMVar_hsa_circ_162179,RMVar_hsa_circ_162178 21060 RMVar_ID_21060 Human_SNP_ID_523245206 A-to-I Human chr13 - 21499613 21499613 21499613 GAGGTCAGAAGATTGAGAACATCTTGGCTAACATGGTGAAACCCCATCTCTACTAAAAATACAAA GAGGTCAGAAGATTGAGAACATCTTGGCTAACGTGGTGAAACCCCATCTCTACTAAAAATACAAA T C MICU2 Ensembl:ENSG00000165487 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs988075110 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_162177,RMVar_hsa_circ_103999,RMVar_hsa_circ_162179,RMVar_hsa_circ_162178 21061 RMVar_ID_21061 Human_SNP_ID_523245522 A-to-I Human chr13 - 21500623 21500623 21500623 CTCAAGGTCAGGAGTTCGAGACTAGCCGGGCCAACATGGTGAAACCCCATCTCTACCAAAAAATA CTCAAGGTCAGGAGTTCGAGACTAGCCGGGCCGACATGGTGAAACCCCATCTCTACCAAAAAATA T C MICU2 Ensembl:ENSG00000165487 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1406498007 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_162177,RMVar_hsa_circ_103999,RMVar_hsa_circ_162179,RMVar_hsa_circ_162178 21062 RMVar_ID_21062 Human_SNP_ID_523245892 A-to-I Human chr13 - 21501868 21501868 21501868 CTCTGTCCGCATAGAGGTCTAGACCCATTCAGAGGTCTAGACTCTCTGAGGCTGTGCCATCTTGG CTCTGTCCGCATAGAGGTCTAGACCCATTCAGGGGTCTAGACTCTCTGAGGCTGTGCCATCTTGG T C MICU2 Ensembl:ENSG00000165487 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1199948 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_1932,GWAS_ID_1933,GWAS_ID_1934,GWAS_ID_1935,GWAS_ID_1936,GWAS_ID_1937,GWAS_ID_1938,GWAS_ID_1939,GWAS_ID_1940,GWAS_ID_1941,GWAS_ID_1942,GWAS_ID_1943,GWAS_ID_1944,GWAS_ID_1945,GWAS_ID_1946,GWAS_ID_1947,GWAS_ID_1948,GWAS_ID_1949,GWAS_ID_1950,GWAS_ID_1951,GWAS_ID_1952,GWAS_ID_1953,GWAS_ID_1954,GWAS_ID_1955,GWAS_ID_1956 RMVar_hsa_circ_162177,RMVar_hsa_circ_103999,RMVar_hsa_circ_162179,RMVar_hsa_circ_162178 21063 RMVar_ID_21063 Human_SNP_ID_523277501 A-to-I Human chr13 - 21628657 21628657 21628657 TACAAAAAATAAGCAAAAGCGTCCCAGGAGCCATACTCTGACAGCTGTGCACGATGCCATCCTTG TACAAAAAATAAGCAAAAGCGTCCCAGGAGCCGTACTCTGACAGCTGTGCACGATGCCATCCTTG T C RPS7P10 Ensembl:ENSG00000226525 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs747280665 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_433264,Human_RBP_ID_17361117 Human_miRNA_ID_1887709,Human_miRNA_ID_1887753,Human_miRNA_ID_1887797 21064 RMVar_ID_21064 Human_SNP_ID_523724494 A-to-I Human chr13 - 23331379 23331379 23331379 GCCTGGCACACCAATTCCTGCTGAAATTCATTACACTCTGCTTATGGACCCAATGAATGTTTTTT GCCTGGCACACCAATTCCTGCTGAAATTCATTTCACTCTGCTTATGGACCCAATGAATGTTTTTT T A SACS Ensembl:ENSG00000151835 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1184350049 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8788758,Human_RBP_ID_12115945,Human_RBP_ID_17244219,Human_RBP_ID_17359202,Human_RBP_ID_18637868,Human_RBP_ID_26617843,Human_RBP_ID_27220313 RMVar_hsa_circ_95202,RMVar_hsa_circ_162197 21065 RMVar_ID_21065 Human_SNP_ID_524005969 A-to-I Human chr13 - 24440995 24440994 24440996 TGGTGGTGCTTGCCTGTAGTCCCAGCTACTCAAGAGGCTGTGGCAGGAGGATGCTTGCACCTAGG TGGTGGTGCTTGCCTGTAGTCCCAGCTACTC__GAGGCTGTGGCAGGAGGATGCTTGCACCTAGG CTT C PARP4 Ensembl:ENSG00000102699 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1418431331 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_78855,RMVar_hsa_circ_61614,RMVar_hsa_circ_80568,RMVar_hsa_circ_162236,RMVar_hsa_circ_162237 21066 RMVar_ID_21066 Human_SNP_ID_524017616 A-to-I Human chr13 - 24483712 24483712 24483712 TGAGGCAGGAGACTGGCTTGAACCTAGGAGGCAGAGATTGCAGTGAGCTGAGATGGTGCCACTGC TGAGGCAGGAGACTGGCTTGAACCTAGGAGGCGGAGATTGCAGTGAGCTGAGATGGTGCCACTGC T C PARP4 Ensembl:ENSG00000102699 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251981096 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25039211 RMVar_hsa_circ_26331,RMVar_hsa_circ_101343,RMVar_hsa_circ_162238,RMVar_hsa_circ_102757,RMVar_hsa_circ_86516,RMVar_hsa_circ_162239,RMVar_hsa_circ_162240,RMVar_hsa_circ_162241,RMVar_hsa_circ_372654,RMVar_hsa_circ_315445,RMVar_hsa_circ_119446,RMVar_hsa_circ_124526,RMVar_hsa_circ_104242,RMVar_hsa_circ_64311,RMVar_hsa_circ_162244,RMVar_hsa_circ_162246,RMVar_hsa_circ_162247,RMVar_hsa_circ_162248,RMVar_hsa_circ_162245,RMVar_hsa_circ_122839,RMVar_hsa_circ_375140,RMVar_hsa_circ_162249,RMVar_hsa_circ_162250,RMVar_hsa_circ_338757,RMVar_hsa_circ_354665,RMVar_hsa_circ_162256,RMVar_hsa_circ_91967,RMVar_hsa_circ_94008,RMVar_hsa_circ_85275,RMVar_hsa_circ_47758,RMVar_hsa_circ_121043,RMVar_hsa_circ_162258,RMVar_hsa_circ_162259,RMVar_hsa_circ_162257,RMVar_hsa_circ_62096,RMVar_hsa_circ_62699,RMVar_hsa_circ_162261,RMVar_hsa_circ_373722,RMVar_hsa_circ_59142,RMVar_hsa_circ_162264,RMVar_hsa_circ_368783,RMVar_hsa_circ_63155,RMVar_hsa_circ_162262,RMVar_hsa_circ_374742,RMVar_hsa_circ_373348,RMVar_hsa_circ_358850,RMVar_hsa_circ_359729,RMVar_hsa_circ_350316,RMVar_hsa_circ_64138,RMVar_hsa_circ_274646,RMVar_hsa_circ_162265,RMVar_hsa_circ_162266,RMVar_hsa_circ_162267,RMVar_hsa_circ_85444 21067 RMVar_ID_21067 Human_SNP_ID_524025300 A-to-I Human chr13 - 24511067 24511067 24511067 GTTTTTACTCTGGGCCGGGCGTGGCAGCTCACACCTGTAACCCCAGCACTCTGGGAGGCTGAGGC GTTTTTACTCTGGGCCGGGCGTGGCAGCTCACGCCTGTAACCCCAGCACTCTGGGAGGCTGAGGC T C PARP4 Ensembl:ENSG00000102699 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs967511395 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102757,RMVar_hsa_circ_162241 21068 RMVar_ID_21068 Human_SNP_ID_524134769 A-to-I Human chr13 - 24932454 24932454 24932454 TTTTTGGGAGGGAGATGGAGTCTCACTCTGACACCCAGGCTGGAGTACAGTGGTGTGATCTCAGC TTTTTGGGAGGGAGATGGAGTCTCACTCTGACGCCCAGGCTGGAGTACAGTGGTGTGATCTCAGC T C TPTE2P1 Ensembl:ENSG00000253771 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1303632291 Functional Loss SNV dbSNP153 33..33 33 - - - 21069 RMVar_ID_21069 Human_SNP_ID_524134770 A-to-I Human chr13 - 24932454 24932454 24932454 TTTTTGGGAGGGAGATGGAGTCTCACTCTGACACCCAGGCTGGAGTACAGTGGTGTGATCTCAGC TTTTTGGGAGGGAGATGGAGTCTCACTCTGACCCCCAGGCTGGAGTACAGTGGTGTGATCTCAGC T G TPTE2P1 Ensembl:ENSG00000253771 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1303632291 Functional Loss SNV dbSNP153 33..33 33 - - - 21070 RMVar_ID_21070 Human_SNP_ID_524177956 A-to-I Human chr13 + 25096398 25096398 25096398 TGTGAACTTCCAGCATACGAAGGACGCGGAGCATGCTCTGGACACCATGAATTTTGATGTTATAA TGTGAACTTCCAGCATACGAAGGACGCGGAGCGTGCTCTGGACACCATGAATTTTGATGTTATAA A G PABPC3 Ensembl:ENSG00000151846 Protein coding CDS GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1269165434 Functional Loss SNV dbSNP153 33..33 33 - - - 21071 RMVar_ID_21071 Human_SNP_ID_524178507 A-to-I Human chr13 + 25097436 25097436 25097436 CTTCATGACAGCTGTCCCACAGACTCAGAACCATGCTGCATACTATCCTCCTAGCCAAATTGCTC CTTCATGACAGCTGTCCCACAGACTCAGAACCGTGCTGCATACTATCCTCCTAGCCAAATTGCTC A G PABPC3 Ensembl:ENSG00000151846 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs767843616 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_40970,Human_miRNA_ID_69690 21072 RMVar_ID_21072 Human_SNP_ID_524178780 A-to-I Human chr13 - 25097966 25097966 25097966 AGAACGGAGTGACTCTGGAGACTCGAGCATATAAAGAAGTTCTGAATTATCAATCTCCAACAACA AGAACGGAGTGACTCTGGAGACTCGAGCATATTAAGAAGTTCTGAATTATCAATCTCCAACAACA T A - - Other Unknown GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs779122561 Functional Loss SNV dbSNP153 33..33 33 - - - 21073 RMVar_ID_21073 Human_SNP_ID_524178781 A-to-I Human chr13 - 25097966 25097966 25097966 AGAACGGAGTGACTCTGGAGACTCGAGCATATAAAGAAGTTCTGAATTATCAATCTCCAACAACA AGAACGGAGTGACTCTGGAGACTCGAGCATATGAAGAAGTTCTGAATTATCAATCTCCAACAACA T C - - Other Unknown GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs779122561 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 21074 RMVar_ID_21074 Human_SNP_ID_524178826 A-to-I Human chr13 + 25098050 25098050 25098050 CTGTACTACAAGCCCACCAAGCTAAAGAGGCTACCCAGAAAGCAGTTAACAGTGCTACCGGTGTT CTGTACTACAAGCCCACCAAGCTAAAGAGGCTGCCCAGAAAGCAGTTAACAGTGCTACCGGTGTT A G PABPC3 Ensembl:ENSG00000151846 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs999778271 Functional Loss SNV dbSNP153 33..33 33 - - - 21075 RMVar_ID_21075 Human_SNP_ID_524178827 A-to-I Human chr13 + 25098050 25098050 25098050 CTGTACTACAAGCCCACCAAGCTAAAGAGGCTACCCAGAAAGCAGTTAACAGTGCTACCGGTGTT CTGTACTACAAGCCCACCAAGCTAAAGAGGCTTCCCAGAAAGCAGTTAACAGTGCTACCGGTGTT A T PABPC3 Ensembl:ENSG00000151846 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs999778271 Functional Loss SNV dbSNP153 33..33 33 - - - 21076 RMVar_ID_21076 Human_SNP_ID_524233635 A-to-I Human chr13 + 25314153 25314153 25314153 AGGGGGTTCACCATGTTGGCCAAGCTGGTCTCAAACTTCTGACCTCAAGTGATCCGGCTGCCTTG AGGGGGTTCACCATGTTGGCCAAGCTGGTCTCGAACTTCTGACCTCAAGTGATCCGGCTGCCTTG A G NUP58 Ensembl:ENSG00000139496 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs527567050 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8009,RMVar_hsa_circ_45771,RMVar_hsa_circ_315788,RMVar_hsa_circ_355135,RMVar_hsa_circ_360658,RMVar_hsa_circ_318333,RMVar_hsa_circ_303930,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,RMVar_hsa_circ_162307,RMVar_hsa_circ_80243,RMVar_hsa_circ_279649,RMVar_hsa_circ_306580,RMVar_hsa_circ_123453,RMVar_hsa_circ_32423,RMVar_hsa_circ_62958,RMVar_hsa_circ_162309,RMVar_hsa_circ_10043,RMVar_hsa_circ_162308,RMVar_hsa_circ_162306 21077 RMVar_ID_21077 Human_SNP_ID_524233725 A-to-I Human chr13 + 25314486 25314486 25314486 GGGAGGCCAAGGCAGGTGGGTCATCTGAGGTCAGGAGTTCGAGACCAGCCTGACCAACATGGTGA GGGAGGCCAAGGCAGGTGGGTCATCTGAGGTCGGGAGTTCGAGACCAGCCTGACCAACATGGTGA A G NUP58 Ensembl:ENSG00000139496 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1266105393 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8009,RMVar_hsa_circ_45771,RMVar_hsa_circ_315788,RMVar_hsa_circ_355135,RMVar_hsa_circ_360658,RMVar_hsa_circ_318333,RMVar_hsa_circ_303930,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,RMVar_hsa_circ_162307,RMVar_hsa_circ_80243,RMVar_hsa_circ_279649,RMVar_hsa_circ_306580,RMVar_hsa_circ_123453,RMVar_hsa_circ_32423,RMVar_hsa_circ_62958,RMVar_hsa_circ_162309,RMVar_hsa_circ_10043,RMVar_hsa_circ_162308,RMVar_hsa_circ_162306 21078 RMVar_ID_21078 Human_SNP_ID_524234333 A-to-I Human chr13 + 25316919 25316918 25316919 ATAAATGTCTTAGATATGACATTAAATTTTATAAATATTTATGTACACACAAACATGTATATAAA ATAAATGTCTTAGATATGACATTAAATTTTAT_AATATTTATGTACACACAAACATGTATATAAA TA T NUP58 Ensembl:ENSG00000139496 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1398257692 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_45771,RMVar_hsa_circ_355135,RMVar_hsa_circ_360658,RMVar_hsa_circ_318333,RMVar_hsa_circ_303930,RMVar_hsa_circ_300921,RMVar_hsa_circ_162298,RMVar_hsa_circ_162300,RMVar_hsa_circ_162299,RMVar_hsa_circ_162296,RMVar_hsa_circ_162297,RMVar_hsa_circ_330721,RMVar_hsa_circ_162307,RMVar_hsa_circ_80243,RMVar_hsa_circ_279649,RMVar_hsa_circ_123453,RMVar_hsa_circ_32423,RMVar_hsa_circ_62958,RMVar_hsa_circ_162309,RMVar_hsa_circ_10043,RMVar_hsa_circ_162308,RMVar_hsa_circ_38060,RMVar_hsa_circ_56747 21079 RMVar_ID_21079 Human_SNP_ID_524234334 A-to-I Human chr13 + 25316919 25316919 25316919 ATAAATGTCTTAGATATGACATTAAATTTTATAAATATTTATGTACACACAAACATGTATATAAA ATAAATGTCTTAGATATGACATTAAATTTTATGAATATTTATGTACACACAAACATGTATATAAA A G NUP58 Ensembl:ENSG00000139496 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1163728127 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45771,RMVar_hsa_circ_355135,RMVar_hsa_circ_360658,RMVar_hsa_circ_318333,RMVar_hsa_circ_303930,RMVar_hsa_circ_300921,RMVar_hsa_circ_162298,RMVar_hsa_circ_162300,RMVar_hsa_circ_162299,RMVar_hsa_circ_162296,RMVar_hsa_circ_162297,RMVar_hsa_circ_330721,RMVar_hsa_circ_162307,RMVar_hsa_circ_80243,RMVar_hsa_circ_279649,RMVar_hsa_circ_123453,RMVar_hsa_circ_32423,RMVar_hsa_circ_62958,RMVar_hsa_circ_162309,RMVar_hsa_circ_10043,RMVar_hsa_circ_162308,RMVar_hsa_circ_38060,RMVar_hsa_circ_56747 21080 RMVar_ID_21080 Human_SNP_ID_524234351 A-to-I Human chr13 + 25316970 25316970 25316970 AACATGTATATAAATAACTTGGGTGTGTTTCTACTATGGATCTCTGATTACTACATCCCAGTTCC AACATGTATATAAATAACTTGGGTGTGTTTCTGCTATGGATCTCTGATTACTACATCCCAGTTCC A G NUP58 Ensembl:ENSG00000139496 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs994900491 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45771,RMVar_hsa_circ_355135,RMVar_hsa_circ_360658,RMVar_hsa_circ_318333,RMVar_hsa_circ_303930,RMVar_hsa_circ_300921,RMVar_hsa_circ_162298,RMVar_hsa_circ_162300,RMVar_hsa_circ_162299,RMVar_hsa_circ_162296,RMVar_hsa_circ_162297,RMVar_hsa_circ_330721,RMVar_hsa_circ_162307,RMVar_hsa_circ_80243,RMVar_hsa_circ_279649,RMVar_hsa_circ_123453,RMVar_hsa_circ_32423,RMVar_hsa_circ_62958,RMVar_hsa_circ_162309,RMVar_hsa_circ_10043,RMVar_hsa_circ_162308,RMVar_hsa_circ_38060,RMVar_hsa_circ_56747 21081 RMVar_ID_21081 Human_SNP_ID_524234703 A-to-I Human chr13 + 25318260 25318260 25318260 TGAGGCAGGAGAATTGCTTGAACCTGGGCAGCAGAGGTTGCAGTGAGCTGAGATCACGCCACTGC TGAGGCAGGAGAATTGCTTGAACCTGGGCAGCGGAGGTTGCAGTGAGCTGAGATCACGCCACTGC A G NUP58 Ensembl:ENSG00000139496 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1015354834 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45771,RMVar_hsa_circ_355135,RMVar_hsa_circ_360658,RMVar_hsa_circ_318333,RMVar_hsa_circ_303930,RMVar_hsa_circ_300921,RMVar_hsa_circ_162298,RMVar_hsa_circ_162300,RMVar_hsa_circ_162299,RMVar_hsa_circ_162296,RMVar_hsa_circ_162297,RMVar_hsa_circ_330721,RMVar_hsa_circ_162307,RMVar_hsa_circ_80243,RMVar_hsa_circ_279649,RMVar_hsa_circ_123453,RMVar_hsa_circ_32423,RMVar_hsa_circ_62958,RMVar_hsa_circ_162309,RMVar_hsa_circ_10043,RMVar_hsa_circ_162308,RMVar_hsa_circ_38060,RMVar_hsa_circ_56747 21082 RMVar_ID_21082 Human_SNP_ID_524273923 A-to-I Human chr13 + 25476450 25476450 25476450 AGCTGCGATTACAGGCACCCGCCACCACGGCCAGCTAATTTTTGAATTTTTGGTAGAGAACGGGG AGCTGCGATTACAGGCACCCGCCACCACGGCCGGCTAATTTTTGAATTTTTGGTAGAGAACGGGG A G ATP8A2 Ensembl:ENSG00000132932 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1272526608 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17985,RMVar_hsa_circ_51956,RMVar_hsa_circ_52631,RMVar_hsa_circ_18869,RMVar_hsa_circ_162320,RMVar_hsa_circ_17571,RMVar_hsa_circ_162319 21083 RMVar_ID_21083 Human_SNP_ID_524476323 A-to-I Human chr13 + 26302149 26302149 26302149 ATAAACCTGATAAACTTCTGGATTAATCAAGGACTATGCTATTTAAAGTACCCATAAAACACCCC ATAAACCTGATAAACTTCTGGATTAATCAAGGGCTATGCTATTTAAAGTACCCATAAAACACCCC A G CDK8 Ensembl:ENSG00000132964 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1168166148 Functional Loss SNV dbSNP153 33..33 33 - - - 21084 RMVar_ID_21084 Human_SNP_ID_524476325 A-to-I Human chr13 + 26302152 26302152 26302152 AACCTGATAAACTTCTGGATTAATCAAGGACTATGCTATTTAAAGTACCCATAAAACACCCCAAT AACCTGATAAACTTCTGGATTAATCAAGGACTGTGCTATTTAAAGTACCCATAAAACACCCCAAT A G CDK8 Ensembl:ENSG00000132964 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs769386117 Functional Loss SNV dbSNP153 33..33 33 - - - 21085 RMVar_ID_21085 Human_SNP_ID_524491778 A-to-I Human chr13 + 26369587 26369587 26369587 GTCTCGCTCTGTCACCCAGGCTGGAGTGCAGTAGCGTGATCTCCGCTCACTGCAAGCTCCGCTTC GTCTCGCTCTGTCACCCAGGCTGGAGTGCAGTGGCGTGATCTCCGCTCACTGCAAGCTCCGCTTC A G CDK8 Ensembl:ENSG00000132964 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs111672686 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28633,RMVar_hsa_circ_47183,RMVar_hsa_circ_320377,RMVar_hsa_circ_364825,RMVar_hsa_circ_25206,RMVar_hsa_circ_342130,RMVar_hsa_circ_162362,RMVar_hsa_circ_375091,RMVar_hsa_circ_29331,RMVar_hsa_circ_162365,RMVar_hsa_circ_162366,RMVar_hsa_circ_34812 21086 RMVar_ID_21086 Human_SNP_ID_524712667 A-to-I Human chr13 - 27246588 27246588 27246588 GCGCCCATAGTCCCAGCTGCTTGCGGGGCTGAAGCAGGAGAATCACTTGGGCCCAGAGGTTGAGG GCGCCCATAGTCCCAGCTGCTTGCGGGGCTGAGGCAGGAGAATCACTTGGGCCCAGAGGTTGAGG T C LINC02340,LINC00412 Ensembl:ENSG00000275294,Ensembl:ENSG00000234772 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs921183854 Functional Loss SNV dbSNP153 33..33 33 - - - 21087 RMVar_ID_21087 Human_SNP_ID_524716253 A-to-I Human chr13 + 27257779 27257779 27257779 ACAAAAATGAGCCTGCCATCGTGAGCACCTGTAATCCCAGCTGCTCTGGAGGCTGAGGCAAGAGA ACAAAAATGAGCCTGCCATCGTGAGCACCTGTGATCCCAGCTGCTCTGGAGGCTGAGGCAAGAGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1276480328 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12120933 21088 RMVar_ID_21088 Human_SNP_ID_524763670 A-to-I Human chr13 - 27438269 27438269 27438269 ATGTTGCTCAGGTCTTGAACTCCTGAGCTCCAACGATCTGCCTGCTTCAGCCTCCCAAAGTGCTG ATGTTGCTCAGGTCTTGAACTCCTGAGCTCCAGCGATCTGCCTGCTTCAGCCTCCCAAAGTGCTG T C MTIF3 Ensembl:ENSG00000122033 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs954766733 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17561979 RMVar_hsa_circ_325919 21089 RMVar_ID_21089 Human_SNP_ID_524763730 A-to-I Human chr13 - 27438403 27438403 27438403 TCACTGCAGCCTCCATCTCCTGGGATCCAGCAATCCTCCCACCTCTGCCTCCCACACAGCTGGGA TCACTGCAGCCTCCATCTCCTGGGATCCAGCAGTCCTCCCACCTCTGCCTCCCACACAGCTGGGA T C MTIF3 Ensembl:ENSG00000122033 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs145644047 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_325919 21090 RMVar_ID_21090 Human_SNP_ID_524790023 A-to-I Human chr13 - 27543535 27543535 27543535 TTGAGGTCAGGAATTTGAGACCAGCCCGTCCAACATGGTGAAACCTCGTCTCTACTAAAAATACA TTGAGGTCAGGAATTTGAGACCAGCCCGTCCAGCATGGTGAAACCTCGTCTCTACTAAAAATACA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1187517925 Functional Loss SNV dbSNP153 33..33 33 - - - 21091 RMVar_ID_21091 Human_SNP_ID_524817216 A-to-I Human chr13 + 27651638 27651638 27651638 GTAAATAATAGATATATTATTTTAAAGTGAATACTGAAAAAAATGCTCAGCTTTAATTTTGAATA GTAAATAATAGATATATTATTTTAAAGTGAATGCTGAAAAAAATGCTCAGCTTTAATTTTGAATA A G POLR1D Ensembl:ENSG00000186184 Protein coding intron GSE38233;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;Bronchiolar epithelium,BERP35T4 cell line - 24183664,31158229 RNA-Seq:(High) rs1359133706 Functional Loss SNV dbSNP153 33..33 33 - - - 21092 RMVar_ID_21092 Human_SNP_ID_524817242 A-to-I Human chr13 + 27651782 27651782 27651782 GTACCCTAAGACCACAAAGTTTGAGAACCACTATTATAAGACAATTGAAAAAAATAAGAATGCCA GTACCCTAAGACCACAAAGTTTGAGAACCACTGTTATAAGACAATTGAAAAAAATAAGAATGCCA A G POLR1D Ensembl:ENSG00000186184 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7336858 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_1957,GWAS_ID_1958,GWAS_ID_1959,GWAS_ID_1960,GWAS_ID_1961,GWAS_ID_1962,GWAS_ID_1963,GWAS_ID_1964,GWAS_ID_1965,GWAS_ID_1966,GWAS_ID_1967,GWAS_ID_1968,GWAS_ID_1969,GWAS_ID_1970,GWAS_ID_1971,GWAS_ID_1972,GWAS_ID_1973 21093 RMVar_ID_21093 Human_SNP_ID_524817323 A-to-I Human chr13 + 27652129 27652129 27652129 CCAATCTAATACCTATTAGAAAGACTCAGCATAGAGTTAAAATCATGCAATTTACAAGTGAGTAA CCAATCTAATACCTATTAGAAAGACTCAGCATGGAGTTAAAATCATGCAATTTACAAGTGAGTAA A G POLR1D Ensembl:ENSG00000186184 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1002623698 Functional Loss SNV dbSNP153 33..33 33 - - - 21094 RMVar_ID_21094 Human_SNP_ID_524817335 A-to-I Human chr13 + 27652168 27652168 27652168 AAATCATGCAATTTACAAGTGAGTAAGAAAATATCAATTATAGTTCTTGCTCTGTAAGGAGCGTT AAATCATGCAATTTACAAGTGAGTAAGAAAATGTCAATTATAGTTCTTGCTCTGTAAGGAGCGTT A G POLR1D Ensembl:ENSG00000186184 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1163057151 Functional Loss SNV dbSNP153 33..33 33 - - - 21095 RMVar_ID_21095 Human_SNP_ID_524817337 A-to-I Human chr13 + 27652171 27652171 27652171 TCATGCAATTTACAAGTGAGTAAGAAAATATCAATTATAGTTCTTGCTCTGTAAGGAGCGTTCAA TCATGCAATTTACAAGTGAGTAAGAAAATATCTATTATAGTTCTTGCTCTGTAAGGAGCGTTCAA A T POLR1D Ensembl:ENSG00000186184 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1041715467 Functional Loss SNV dbSNP153 33..33 33 - - - 21096 RMVar_ID_21096 Human_SNP_ID_524817355 A-to-I Human chr13 + 27652244 27652244 27652244 GTTGTTTCTTGCCAGCTCTCCAGATAGACATCATTTATCCTGACAACTTTAGTACCACCTACTGG GTTGTTTCTTGCCAGCTCTCCAGATAGACATCGTTTATCCTGACAACTTTAGTACCACCTACTGG A G POLR1D Ensembl:ENSG00000186184 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs918272694 Functional Loss SNV dbSNP153 33..33 33 - - - 21097 RMVar_ID_21097 Human_SNP_ID_524817356 A-to-I Human chr13 + 27652244 27652244 27652244 GTTGTTTCTTGCCAGCTCTCCAGATAGACATCATTTATCCTGACAACTTTAGTACCACCTACTGG GTTGTTTCTTGCCAGCTCTCCAGATAGACATCTTTTATCCTGACAACTTTAGTACCACCTACTGG A T POLR1D Ensembl:ENSG00000186184 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs918272694 Functional Loss SNV dbSNP153 33..33 33 - - - 21098 RMVar_ID_21098 Human_SNP_ID_524817477 A-to-I Human chr13 + 27652749 27652748 27652749 AAAATTAGCCAGATGTGCTGGCACACGTCTGTAATCCCAGCTACTCAGGCTGAGGCAGGAGAATC AAAATTAGCCAGATGTGCTGGCACACGTCTGT_ATCCCAGCTACTCAGGCTGAGGCAGGAGAATC TA T POLR1D Ensembl:ENSG00000186184 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1224182540 Functional Loss DEL dbSNP153 33..33 33 - - - 21099 RMVar_ID_21099 Human_SNP_ID_524817506 A-to-I Human chr13 + 27652862 27652862 27652862 GCACTCCAGCCTGGGGGACACAGTGAGACTCCATCTCAAAAAAAAAAAAAGAAAACTTGCCAGAA GCACTCCAGCCTGGGGGACACAGTGAGACTCCCTCTCAAAAAAAAAAAAAGAAAACTTGCCAGAA A C POLR1D Ensembl:ENSG00000186184 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1309972551 Functional Loss SNV dbSNP153 33..33 33 - - - 21100 RMVar_ID_21100 Human_SNP_ID_524817596 A-to-I Human chr13 + 27653016 27653016 27653016 CTGCCTCCCTGGTGCAAGCAATTCTCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGTGCCCA CTGCCTCCCTGGTGCAAGCAATTCTCTGCCTCGGCCTCCCGAGTAGCTGGGATTACAGGTGCCCA A G POLR1D Ensembl:ENSG00000186184 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs998172356 Functional Loss SNV dbSNP153 33..33 33 - - - 21101 RMVar_ID_21101 Human_SNP_ID_524817634 A-to-I Human chr13 + 27653161 27653161 27653161 CTGACCTAGTGATCGCCTGCCTTGGCCTCCCAAAGTGCTAGGATTGCAGGCGTGAGCCACCGTGC CTGACCTAGTGATCGCCTGCCTTGGCCTCCCAGAGTGCTAGGATTGCAGGCGTGAGCCACCGTGC A G POLR1D Ensembl:ENSG00000186184 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs998615993 Functional Loss SNV dbSNP153 33..33 33 - - - 21102 RMVar_ID_21102 Human_SNP_ID_524817715 A-to-I Human chr13 + 27653508 27653508 27653508 GAGACTAGGATGTGAAATTACACTTTCCCATGAGTCTGAAAGACACGAATTCCTGCTGGGATTGT GAGACTAGGATGTGAAATTACACTTTCCCATGGGTCTGAAAGACACGAATTCCTGCTGGGATTGT A G POLR1D Ensembl:ENSG00000186184 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs946278425 Functional Loss SNV dbSNP153 33..33 33 - - - 21103 RMVar_ID_21103 Human_SNP_ID_524817716 A-to-I Human chr13 + 27653515 27653515 27653515 GGATGTGAAATTACACTTTCCCATGAGTCTGAAAGACACGAATTCCTGCTGGGATTGTTACTTGG GGATGTGAAATTACACTTTCCCATGAGTCTGAGAGACACGAATTCCTGCTGGGATTGTTACTTGG A G POLR1D Ensembl:ENSG00000186184 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1031451026 Functional Loss SNV dbSNP153 33..33 33 - - - 21104 RMVar_ID_21104 Human_SNP_ID_524817727 A-to-I Human chr13 + 27653555 27653555 27653555 AATTCCTGCTGGGATTGTTACTTGGTTATCTCAATTGTCTTGGAACAGTGGTTCTCAAACATCTT AATTCCTGCTGGGATTGTTACTTGGTTATCTCGATTGTCTTGGAACAGTGGTTCTCAAACATCTT A G POLR1D Ensembl:ENSG00000186184 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs538246263 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1271832 21105 RMVar_ID_21105 Human_SNP_ID_524817792 A-to-I Human chr13 + 27653907 27653907 27653907 GTGTTATTTTGGCTGAAGTATGTGAAGAAAATACTACCTTACAAAGATATGTATTTTCAAAAGGA GTGTTATTTTGGCTGAAGTATGTGAAGAAAATGCTACCTTACAAAGATATGTATTTTCAAAAGGA A G POLR1D Ensembl:ENSG00000186184 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1566151282 Functional Loss SNV dbSNP153 33..33 33 - - - 21106 RMVar_ID_21106 Human_SNP_ID_524817803 A-to-I Human chr13 + 27653959 27653959 27653959 ATTTTCAAAAGGAAATACATATCAGAAAGTTTAACAAAGCCAGTAGGTGATACTAAAGTTGTCAG ATTTTCAAAAGGAAATACATATCAGAAAGTTTCACAAAGCCAGTAGGTGATACTAAAGTTGTCAG A C POLR1D Ensembl:ENSG00000186184 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1038669450 Functional Loss SNV dbSNP153 33..33 33 - - - 21107 RMVar_ID_21107 Human_SNP_ID_524817804 A-to-I Human chr13 + 27653959 27653959 27653959 ATTTTCAAAAGGAAATACATATCAGAAAGTTTAACAAAGCCAGTAGGTGATACTAAAGTTGTCAG ATTTTCAAAAGGAAATACATATCAGAAAGTTTTACAAAGCCAGTAGGTGATACTAAAGTTGTCAG A T POLR1D Ensembl:ENSG00000186184 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1038669450 Functional Loss SNV dbSNP153 33..33 33 - - - 21108 RMVar_ID_21108 Human_SNP_ID_524817806 A-to-I Human chr13 + 27653971 27653971 27653971 AAATACATATCAGAAAGTTTAACAAAGCCAGTAGGTGATACTAAAGTTGTCAGGATAAATGATGT AAATACATATCAGAAAGTTTAACAAAGCCAGTGGGTGATACTAAAGTTGTCAGGATAAATGATGT A G POLR1D Ensembl:ENSG00000186184 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1062351 Functional Loss SNV dbSNP153 33..33 33 - - - 21109 RMVar_ID_21109 Human_SNP_ID_524817810 A-to-I Human chr13 + 27653981 27653981 27653981 CAGAAAGTTTAACAAAGCCAGTAGGTGATACTAAAGTTGTCAGGATAAATGATGTCTATCTGGAG CAGAAAGTTTAACAAAGCCAGTAGGTGATACTGAAGTTGTCAGGATAAATGATGTCTATCTGGAG A G POLR1D Ensembl:ENSG00000186184 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1474385966 Functional Loss SNV dbSNP153 33..33 33 - - - 21110 RMVar_ID_21110 Human_SNP_ID_524817820 A-to-I Human chr13 + 27654021 27654021 27654021 CAGGATAAATGATGTCTATCTGGAGAGCTGGCAAGAAACAACCAAGCCCCTTGAACGCTCCTTAC CAGGATAAATGATGTCTATCTGGAGAGCTGGCCAGAAACAACCAAGCCCCTTGAACGCTCCTTAC A C POLR1D Ensembl:ENSG00000186184 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1226895364 Functional Loss SNV dbSNP153 33..33 33 - - - 21111 RMVar_ID_21111 Human_SNP_ID_524817831 A-to-I Human chr13 + 27654052 27654052 27654052 CAAGAAACAACCAAGCCCCTTGAACGCTCCTTACAGAGCAAGAACTATGATTGATATTTTCTTAC CAAGAAACAACCAAGCCCCTTGAACGCTCCTTGCAGAGCAAGAACTATGATTGATATTTTCTTAC A G POLR1D Ensembl:ENSG00000186184 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1062352 Functional Loss SNV dbSNP153 33..33 33 - - - 21112 RMVar_ID_21112 Human_SNP_ID_524817835 A-to-I Human chr13 + 27654066 27654066 27654066 GCCCCTTGAACGCTCCTTACAGAGCAAGAACTATGATTGATATTTTCTTACTCACTTGTAAATTG GCCCCTTGAACGCTCCTTACAGAGCAAGAACTGTGATTGATATTTTCTTACTCACTTGTAAATTG A G POLR1D Ensembl:ENSG00000186184 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs922118163 Functional Loss SNV dbSNP153 33..33 33 - - - 21113 RMVar_ID_21113 Human_SNP_ID_524817837 A-to-I Human chr13 + 27654075 27654075 27654075 ACGCTCCTTACAGAGCAAGAACTATGATTGATATTTTCTTACTCACTTGTAAATTGCGTGATTTT ACGCTCCTTACAGAGCAAGAACTATGATTGATCTTTTCTTACTCACTTGTAAATTGCGTGATTTT A C POLR1D Ensembl:ENSG00000186184 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs967516678 Functional Loss SNV dbSNP153 33..33 33 - - - 21114 RMVar_ID_21114 Human_SNP_ID_524817845 A-to-I Human chr13 + 27654108 27654108 27654108 TTTTCTTACTCACTTGTAAATTGCGTGATTTTAGCTCTATTTCAATAACTTTTTCAGAAGACTGT TTTTCTTACTCACTTGTAAATTGCGTGATTTTCGCTCTATTTCAATAACTTTTTCAGAAGACTGT A C POLR1D Ensembl:ENSG00000186184 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs770788884 Functional Loss SNV dbSNP153 33..33 33 - - - 21115 RMVar_ID_21115 Human_SNP_ID_524945738 A-to-I Human chr13 + 28149099 28149084 28149099 ACACTGTGTGGGGTGTGGCGACTCATACCTGTAATCCTAGTACTTTGGAAGGCCGAGACAGGAAG ACACTGTGTGGGGTGTGG_______________ATCCTAGTACTTTGGAAGGCCGAGACAGGAAG GCGACTCATACCTGTA G PAN3 Ensembl:ENSG00000152520 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1168169641 Functional Loss DEL dbSNP153 19..33 33 - - - RMVar_hsa_circ_162417,RMVar_hsa_circ_76164,RMVar_hsa_circ_114856,RMVar_hsa_circ_110149,RMVar_hsa_circ_162418,RMVar_hsa_circ_162419,RMVar_hsa_circ_162420,RMVar_hsa_circ_114145 21116 RMVar_ID_21116 Human_SNP_ID_524945743 A-to-I Human chr13 + 28149093 28149093 28149093 AAAAAAACACTGTGTGGGGTGTGGCGACTCATACCTGTAATCCTAGTACTTTGGAAGGCCGAGAC AAAAAAACACTGTGTGGGGTGTGGCGACTCATCCCTGTAATCCTAGTACTTTGGAAGGCCGAGAC A C PAN3 Ensembl:ENSG00000152520 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs988294800 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_162417,RMVar_hsa_circ_76164,RMVar_hsa_circ_114856,RMVar_hsa_circ_110149,RMVar_hsa_circ_162418,RMVar_hsa_circ_162419,RMVar_hsa_circ_162420,RMVar_hsa_circ_114145 21117 RMVar_ID_21117 Human_SNP_ID_524945883 A-to-I Human chr13 + 28149715 28149715 28149715 CTCACTGCATGCACCCTTGAACTCCTGGGCTCAAGTTACCCTCTTGCCTCAGCCTCCTTAGTAGT CTCACTGCATGCACCCTTGAACTCCTGGGCTCGAGTTACCCTCTTGCCTCAGCCTCCTTAGTAGT A G PAN3 Ensembl:ENSG00000152520 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1566136849 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_162417,RMVar_hsa_circ_76164,RMVar_hsa_circ_114856,RMVar_hsa_circ_110149,RMVar_hsa_circ_162418,RMVar_hsa_circ_162419,RMVar_hsa_circ_162420,RMVar_hsa_circ_114145 21118 RMVar_ID_21118 Human_SNP_ID_524955534 A-to-I Human chr13 + 28187833 28187833 28187833 TCCTGTCTCATCTACCCAACTTAGCTGGGACTACAGGCACATGCCACCATGCCCAGCTAATTTTT TCCTGTCTCATCTACCCAACTTAGCTGGGACTTCAGGCACATGCCACCATGCCCAGCTAATTTTT A T PAN3 Ensembl:ENSG00000152520 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs998894405 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49856,RMVar_hsa_circ_88548,RMVar_hsa_circ_127771,RMVar_hsa_circ_162417,RMVar_hsa_circ_76164,RMVar_hsa_circ_114856,RMVar_hsa_circ_110149,RMVar_hsa_circ_162418,RMVar_hsa_circ_162419,RMVar_hsa_circ_309106,RMVar_hsa_circ_339660,RMVar_hsa_circ_295667,RMVar_hsa_circ_270128,RMVar_hsa_circ_162421,RMVar_hsa_circ_162425,RMVar_hsa_circ_50550,RMVar_hsa_circ_122980,RMVar_hsa_circ_162426,RMVar_hsa_circ_162423,RMVar_hsa_circ_162424,RMVar_hsa_circ_162422,RMVar_hsa_circ_93674,RMVar_hsa_circ_337001,RMVar_hsa_circ_117709,RMVar_hsa_circ_90916,RMVar_hsa_circ_162431,RMVar_hsa_circ_162433,RMVar_hsa_circ_162435,RMVar_hsa_circ_162434,RMVar_hsa_circ_162432,RMVar_hsa_circ_115771,RMVar_hsa_circ_96660,RMVar_hsa_circ_162437,RMVar_hsa_circ_14598,RMVar_hsa_circ_162436 21119 RMVar_ID_21119 Human_SNP_ID_524955535 A-to-I Human chr13 + 28187835 28187835 28187835 CTGTCTCATCTACCCAACTTAGCTGGGACTACAGGCACATGCCACCATGCCCAGCTAATTTTTTA CTGTCTCATCTACCCAACTTAGCTGGGACTACGGGCACATGCCACCATGCCCAGCTAATTTTTTA A G PAN3 Ensembl:ENSG00000152520 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1412777657 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49856,RMVar_hsa_circ_88548,RMVar_hsa_circ_127771,RMVar_hsa_circ_162417,RMVar_hsa_circ_76164,RMVar_hsa_circ_114856,RMVar_hsa_circ_110149,RMVar_hsa_circ_162418,RMVar_hsa_circ_162419,RMVar_hsa_circ_309106,RMVar_hsa_circ_339660,RMVar_hsa_circ_295667,RMVar_hsa_circ_270128,RMVar_hsa_circ_162421,RMVar_hsa_circ_162425,RMVar_hsa_circ_50550,RMVar_hsa_circ_122980,RMVar_hsa_circ_162426,RMVar_hsa_circ_162423,RMVar_hsa_circ_162424,RMVar_hsa_circ_162422,RMVar_hsa_circ_93674,RMVar_hsa_circ_337001,RMVar_hsa_circ_117709,RMVar_hsa_circ_90916,RMVar_hsa_circ_162431,RMVar_hsa_circ_162433,RMVar_hsa_circ_162435,RMVar_hsa_circ_162434,RMVar_hsa_circ_162432,RMVar_hsa_circ_115771,RMVar_hsa_circ_96660,RMVar_hsa_circ_162437,RMVar_hsa_circ_14598,RMVar_hsa_circ_162436 21120 RMVar_ID_21120 Human_SNP_ID_524955548 A-to-I Human chr13 + 28187891 28187891 28187891 AATTTTTTAAATTCTTGTGGAGACTGGGTCTCACTCTGTTGCCCAGGCTGGTCTTGAACTCCTGG AATTTTTTAAATTCTTGTGGAGACTGGGTCTCGCTCTGTTGCCCAGGCTGGTCTTGAACTCCTGG A G PAN3 Ensembl:ENSG00000152520 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs970678683 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49856,RMVar_hsa_circ_88548,RMVar_hsa_circ_127771,RMVar_hsa_circ_162417,RMVar_hsa_circ_76164,RMVar_hsa_circ_114856,RMVar_hsa_circ_110149,RMVar_hsa_circ_162418,RMVar_hsa_circ_162419,RMVar_hsa_circ_309106,RMVar_hsa_circ_339660,RMVar_hsa_circ_295667,RMVar_hsa_circ_270128,RMVar_hsa_circ_162421,RMVar_hsa_circ_162425,RMVar_hsa_circ_50550,RMVar_hsa_circ_122980,RMVar_hsa_circ_162426,RMVar_hsa_circ_162423,RMVar_hsa_circ_162424,RMVar_hsa_circ_162422,RMVar_hsa_circ_93674,RMVar_hsa_circ_337001,RMVar_hsa_circ_117709,RMVar_hsa_circ_90916,RMVar_hsa_circ_162431,RMVar_hsa_circ_162433,RMVar_hsa_circ_162435,RMVar_hsa_circ_162434,RMVar_hsa_circ_162432,RMVar_hsa_circ_115771,RMVar_hsa_circ_96660,RMVar_hsa_circ_162437,RMVar_hsa_circ_14598,RMVar_hsa_circ_162436 21121 RMVar_ID_21121 Human_SNP_ID_524955704 A-to-I Human chr13 + 28188552 28188552 28188552 GAGCTCAGGGGTTTGAAGCTGCAATTAGCTATAGTTGGGCCACTGCACTGCAGCCTGGGCAACAG GAGCTCAGGGGTTTGAAGCTGCAATTAGCTATTGTTGGGCCACTGCACTGCAGCCTGGGCAACAG A T PAN3 Ensembl:ENSG00000152520 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1166041142 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6267736,Human_RBP_ID_12123698 RMVar_hsa_circ_49856,RMVar_hsa_circ_88548,RMVar_hsa_circ_127771,RMVar_hsa_circ_162417,RMVar_hsa_circ_76164,RMVar_hsa_circ_114856,RMVar_hsa_circ_110149,RMVar_hsa_circ_162418,RMVar_hsa_circ_162419,RMVar_hsa_circ_309106,RMVar_hsa_circ_339660,RMVar_hsa_circ_295667,RMVar_hsa_circ_270128,RMVar_hsa_circ_162421,RMVar_hsa_circ_162425,RMVar_hsa_circ_50550,RMVar_hsa_circ_122980,RMVar_hsa_circ_162426,RMVar_hsa_circ_162423,RMVar_hsa_circ_162424,RMVar_hsa_circ_162422,RMVar_hsa_circ_93674,RMVar_hsa_circ_337001,RMVar_hsa_circ_117709,RMVar_hsa_circ_90916,RMVar_hsa_circ_162431,RMVar_hsa_circ_162433,RMVar_hsa_circ_162435,RMVar_hsa_circ_162434,RMVar_hsa_circ_162432,RMVar_hsa_circ_115771,RMVar_hsa_circ_96660,RMVar_hsa_circ_162437,RMVar_hsa_circ_14598,RMVar_hsa_circ_162436 21122 RMVar_ID_21122 Human_SNP_ID_524955907 A-to-I Human chr13 + 28189471 28189471 28189471 CCAGGAAGCAGAGGTTGCAGTGAGCCGAGATCATGCCACTGCACTCCAGCCTGGGGCAACAGAGT CCAGGAAGCAGAGGTTGCAGTGAGCCGAGATCGTGCCACTGCACTCCAGCCTGGGGCAACAGAGT A G PAN3 Ensembl:ENSG00000152520 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1437619498 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25040581 RMVar_hsa_circ_49856,RMVar_hsa_circ_88548,RMVar_hsa_circ_127771,RMVar_hsa_circ_162417,RMVar_hsa_circ_76164,RMVar_hsa_circ_114856,RMVar_hsa_circ_110149,RMVar_hsa_circ_162418,RMVar_hsa_circ_162419,RMVar_hsa_circ_309106,RMVar_hsa_circ_339660,RMVar_hsa_circ_295667,RMVar_hsa_circ_270128,RMVar_hsa_circ_162421,RMVar_hsa_circ_162425,RMVar_hsa_circ_50550,RMVar_hsa_circ_122980,RMVar_hsa_circ_162426,RMVar_hsa_circ_162423,RMVar_hsa_circ_162424,RMVar_hsa_circ_162422,RMVar_hsa_circ_93674,RMVar_hsa_circ_337001,RMVar_hsa_circ_117709,RMVar_hsa_circ_90916,RMVar_hsa_circ_162431,RMVar_hsa_circ_162433,RMVar_hsa_circ_162435,RMVar_hsa_circ_162434,RMVar_hsa_circ_162432,RMVar_hsa_circ_115771,RMVar_hsa_circ_96660,RMVar_hsa_circ_162437,RMVar_hsa_circ_14598,RMVar_hsa_circ_162436 21123 RMVar_ID_21123 Human_SNP_ID_524956065 A-to-I Human chr13 + 28190007 28190007 28190007 CTCTTATCACCCAGGCTGGAGTCCAATGACACAATCTTGACTCACTGCAAACTCTGCCCCCCGGG CTCTTATCACCCAGGCTGGAGTCCAATGACACCATCTTGACTCACTGCAAACTCTGCCCCCCGGG A C PAN3 Ensembl:ENSG00000152520 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1209535795 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49856,RMVar_hsa_circ_88548,RMVar_hsa_circ_127771,RMVar_hsa_circ_162417,RMVar_hsa_circ_76164,RMVar_hsa_circ_114856,RMVar_hsa_circ_110149,RMVar_hsa_circ_162418,RMVar_hsa_circ_162419,RMVar_hsa_circ_309106,RMVar_hsa_circ_339660,RMVar_hsa_circ_295667,RMVar_hsa_circ_270128,RMVar_hsa_circ_162421,RMVar_hsa_circ_162425,RMVar_hsa_circ_50550,RMVar_hsa_circ_122980,RMVar_hsa_circ_162426,RMVar_hsa_circ_162423,RMVar_hsa_circ_162424,RMVar_hsa_circ_162422,RMVar_hsa_circ_93674,RMVar_hsa_circ_337001,RMVar_hsa_circ_117709,RMVar_hsa_circ_90916,RMVar_hsa_circ_162431,RMVar_hsa_circ_162433,RMVar_hsa_circ_162435,RMVar_hsa_circ_162434,RMVar_hsa_circ_162432,RMVar_hsa_circ_115771,RMVar_hsa_circ_96660,RMVar_hsa_circ_162437,RMVar_hsa_circ_14598,RMVar_hsa_circ_162436 21124 RMVar_ID_21124 Human_SNP_ID_524956151 A-to-I Human chr13 + 28190310 28190310 28190310 TGTTGGCCAGGTTAGAGTGCAGTGGCACAGTCATAGCCCACTGCAGCTTTGAATTCCTGGGTTAA TGTTGGCCAGGTTAGAGTGCAGTGGCACAGTCGTAGCCCACTGCAGCTTTGAATTCCTGGGTTAA A G PAN3 Ensembl:ENSG00000152520 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1016675084 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49856,RMVar_hsa_circ_88548,RMVar_hsa_circ_127771,RMVar_hsa_circ_162417,RMVar_hsa_circ_76164,RMVar_hsa_circ_114856,RMVar_hsa_circ_110149,RMVar_hsa_circ_162418,RMVar_hsa_circ_162419,RMVar_hsa_circ_309106,RMVar_hsa_circ_339660,RMVar_hsa_circ_295667,RMVar_hsa_circ_270128,RMVar_hsa_circ_162421,RMVar_hsa_circ_162425,RMVar_hsa_circ_50550,RMVar_hsa_circ_122980,RMVar_hsa_circ_162426,RMVar_hsa_circ_162423,RMVar_hsa_circ_162424,RMVar_hsa_circ_162422,RMVar_hsa_circ_93674,RMVar_hsa_circ_337001,RMVar_hsa_circ_117709,RMVar_hsa_circ_90916,RMVar_hsa_circ_162431,RMVar_hsa_circ_162433,RMVar_hsa_circ_162435,RMVar_hsa_circ_162434,RMVar_hsa_circ_162432,RMVar_hsa_circ_115771,RMVar_hsa_circ_96660,RMVar_hsa_circ_162437,RMVar_hsa_circ_14598,RMVar_hsa_circ_162436 21125 RMVar_ID_21125 Human_SNP_ID_524957690 A-to-I Human chr13 + 28195653 28195653 28195653 TGCCTTCCAGGCTCAAGTGATTTTTCTGCCTCAGTCTCCCAAGTAGCTGGGATTACAGACATGTG TGCCTTCCAGGCTCAAGTGATTTTTCTGCCTCGGTCTCCCAAGTAGCTGGGATTACAGACATGTG A G PAN3 Ensembl:ENSG00000152520 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1055651031 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49856,RMVar_hsa_circ_88548,RMVar_hsa_circ_127771,RMVar_hsa_circ_162417,RMVar_hsa_circ_76164,RMVar_hsa_circ_114856,RMVar_hsa_circ_110149,RMVar_hsa_circ_162418,RMVar_hsa_circ_162419,RMVar_hsa_circ_309106,RMVar_hsa_circ_339660,RMVar_hsa_circ_295667,RMVar_hsa_circ_270128,RMVar_hsa_circ_162421,RMVar_hsa_circ_162425,RMVar_hsa_circ_50550,RMVar_hsa_circ_122980,RMVar_hsa_circ_162426,RMVar_hsa_circ_162423,RMVar_hsa_circ_162424,RMVar_hsa_circ_162422,RMVar_hsa_circ_93674,RMVar_hsa_circ_337001,RMVar_hsa_circ_117709,RMVar_hsa_circ_90916,RMVar_hsa_circ_162431,RMVar_hsa_circ_162433,RMVar_hsa_circ_162435,RMVar_hsa_circ_162434,RMVar_hsa_circ_162432,RMVar_hsa_circ_115771,RMVar_hsa_circ_96660,RMVar_hsa_circ_162437,RMVar_hsa_circ_14598,RMVar_hsa_circ_162436 21126 RMVar_ID_21126 Human_SNP_ID_524958200 A-to-I Human chr13 + 28197647 28197647 28197647 CAGGCTGGAGTGCAGTGGCACCATCTTACCTCACTGTAACCTCCACCTCCCAGATTCAAGATACC CAGGCTGGAGTGCAGTGGCACCATCTTACCTCGCTGTAACCTCCACCTCCCAGATTCAAGATACC A G PAN3 Ensembl:ENSG00000152520 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1319630021 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12123917 RMVar_hsa_circ_88548,RMVar_hsa_circ_127771,RMVar_hsa_circ_162417,RMVar_hsa_circ_76164,RMVar_hsa_circ_114856,RMVar_hsa_circ_110149,RMVar_hsa_circ_162418,RMVar_hsa_circ_162419,RMVar_hsa_circ_309106,RMVar_hsa_circ_339660,RMVar_hsa_circ_270128,RMVar_hsa_circ_162421,RMVar_hsa_circ_162425,RMVar_hsa_circ_50550,RMVar_hsa_circ_122980,RMVar_hsa_circ_162423,RMVar_hsa_circ_162424,RMVar_hsa_circ_162422,RMVar_hsa_circ_93674,RMVar_hsa_circ_337001,RMVar_hsa_circ_117709,RMVar_hsa_circ_90916,RMVar_hsa_circ_162431,RMVar_hsa_circ_162433,RMVar_hsa_circ_162435,RMVar_hsa_circ_162434,RMVar_hsa_circ_162432,RMVar_hsa_circ_115771,RMVar_hsa_circ_96660,RMVar_hsa_circ_36076,RMVar_hsa_circ_102181,RMVar_hsa_circ_162437,RMVar_hsa_circ_14598,RMVar_hsa_circ_362293,RMVar_hsa_circ_162436,RMVar_hsa_circ_341016,RMVar_hsa_circ_272193,RMVar_hsa_circ_300203,RMVar_hsa_circ_270914,RMVar_hsa_circ_69082,RMVar_hsa_circ_99954,RMVar_hsa_circ_50689,RMVar_hsa_circ_162440,RMVar_hsa_circ_162442,RMVar_hsa_circ_162443,RMVar_hsa_circ_162441,RMVar_hsa_circ_162439 21127 RMVar_ID_21127 Human_SNP_ID_524974625 A-to-I Human chr13 + 28263472 28263472 28263472 CTCCTACTTCAGCCTCCCAAGTAGCTGGGACTACAGGTGTACACCACCACACTTGGCTAATTTTT CTCCTACTTCAGCCTCCCAAGTAGCTGGGACTGCAGGTGTACACCACCACACTTGGCTAATTTTT A G PAN3 Ensembl:ENSG00000152520 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1310856127 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76164,RMVar_hsa_circ_114856,RMVar_hsa_circ_162418,RMVar_hsa_circ_162419,RMVar_hsa_circ_162421,RMVar_hsa_circ_50550,RMVar_hsa_circ_122980,RMVar_hsa_circ_93674,RMVar_hsa_circ_90916,RMVar_hsa_circ_162435,RMVar_hsa_circ_162434,RMVar_hsa_circ_115771,RMVar_hsa_circ_29869,RMVar_hsa_circ_11438,RMVar_hsa_circ_50113,RMVar_hsa_circ_36076,RMVar_hsa_circ_362293,RMVar_hsa_circ_162436,RMVar_hsa_circ_300203,RMVar_hsa_circ_69082,RMVar_hsa_circ_50689,RMVar_hsa_circ_162443,RMVar_hsa_circ_162447,RMVar_hsa_circ_965,RMVar_hsa_circ_18692,RMVar_hsa_circ_287487,RMVar_hsa_circ_371495,RMVar_hsa_circ_162446,RMVar_hsa_circ_316874,RMVar_hsa_circ_279882,RMVar_hsa_circ_272147,RMVar_hsa_circ_17096,RMVar_hsa_circ_162450,RMVar_hsa_circ_162452,RMVar_hsa_circ_162454,RMVar_hsa_circ_162455,RMVar_hsa_circ_162456,RMVar_hsa_circ_162453,RMVar_hsa_circ_162451,RMVar_hsa_circ_269067,RMVar_hsa_circ_335720,RMVar_hsa_circ_356413,RMVar_hsa_circ_289955,RMVar_hsa_circ_269928,RMVar_hsa_circ_268765,RMVar_hsa_circ_57405,RMVar_hsa_circ_162457,RMVar_hsa_circ_162458 21128 RMVar_ID_21128 Human_SNP_ID_524974629 A-to-I Human chr13 + 28263490 28263490 28263490 AAGTAGCTGGGACTACAGGTGTACACCACCACACTTGGCTAATTTTTGTATATTTTGTAGAGAGG AAGTAGCTGGGACTACAGGTGTACACCACCACGCTTGGCTAATTTTTGTATATTTTGTAGAGAGG A G PAN3 Ensembl:ENSG00000152520 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs959498522 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76164,RMVar_hsa_circ_114856,RMVar_hsa_circ_162418,RMVar_hsa_circ_162419,RMVar_hsa_circ_162421,RMVar_hsa_circ_50550,RMVar_hsa_circ_122980,RMVar_hsa_circ_93674,RMVar_hsa_circ_90916,RMVar_hsa_circ_162435,RMVar_hsa_circ_162434,RMVar_hsa_circ_115771,RMVar_hsa_circ_29869,RMVar_hsa_circ_11438,RMVar_hsa_circ_50113,RMVar_hsa_circ_36076,RMVar_hsa_circ_362293,RMVar_hsa_circ_162436,RMVar_hsa_circ_300203,RMVar_hsa_circ_69082,RMVar_hsa_circ_50689,RMVar_hsa_circ_162443,RMVar_hsa_circ_162447,RMVar_hsa_circ_965,RMVar_hsa_circ_18692,RMVar_hsa_circ_287487,RMVar_hsa_circ_371495,RMVar_hsa_circ_162446,RMVar_hsa_circ_316874,RMVar_hsa_circ_279882,RMVar_hsa_circ_272147,RMVar_hsa_circ_17096,RMVar_hsa_circ_162450,RMVar_hsa_circ_162452,RMVar_hsa_circ_162454,RMVar_hsa_circ_162455,RMVar_hsa_circ_162456,RMVar_hsa_circ_162453,RMVar_hsa_circ_162451,RMVar_hsa_circ_269067,RMVar_hsa_circ_335720,RMVar_hsa_circ_356413,RMVar_hsa_circ_289955,RMVar_hsa_circ_269928,RMVar_hsa_circ_268765,RMVar_hsa_circ_57405,RMVar_hsa_circ_162457,RMVar_hsa_circ_162458 21129 RMVar_ID_21129 Human_SNP_ID_524977010 A-to-I Human chr13 + 28273324 28273324 28273324 TCTTCAAGCATTAAGAACAGTTGCTTTAGGCCAGGTGTGGTGGCTCACACCTGTAATCCCAGCAC TCTTCAAGCATTAAGAACAGTTGCTTTAGGCCGGGTGTGGTGGCTCACACCTGTAATCCCAGCAC A G PAN3 Ensembl:ENSG00000152520 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1487521270 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50550,RMVar_hsa_circ_90916,RMVar_hsa_circ_162435,RMVar_hsa_circ_29869,RMVar_hsa_circ_11438,RMVar_hsa_circ_50113,RMVar_hsa_circ_69082,RMVar_hsa_circ_50689,RMVar_hsa_circ_18692,RMVar_hsa_circ_162446,RMVar_hsa_circ_316874,RMVar_hsa_circ_272147,RMVar_hsa_circ_162455,RMVar_hsa_circ_162456,RMVar_hsa_circ_335720,RMVar_hsa_circ_356413,RMVar_hsa_circ_269928,RMVar_hsa_circ_162467,RMVar_hsa_circ_162457,RMVar_hsa_circ_324082,RMVar_hsa_circ_313867,RMVar_hsa_circ_84604,RMVar_hsa_circ_162469,RMVar_hsa_circ_82987,RMVar_hsa_circ_162470,RMVar_hsa_circ_162468,RMVar_hsa_circ_162471,RMVar_hsa_circ_334895,RMVar_hsa_circ_341678,RMVar_hsa_circ_357735,RMVar_hsa_circ_340753,RMVar_hsa_circ_162476,RMVar_hsa_circ_162477 21130 RMVar_ID_21130 Human_SNP_ID_524978426 A-to-I Human chr13 + 28279504 28279504 28279504 TTTTTTGGCCGGGTGCAGTGGCTCACACCTGTAATCCCAGTGCTTTGGGAGGCCAAGGCAGGTGG TTTTTTGGCCGGGTGCAGTGGCTCACACCTGTGATCCCAGTGCTTTGGGAGGCCAAGGCAGGTGG A G PAN3 Ensembl:ENSG00000152520 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs977550094 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50550,RMVar_hsa_circ_90916,RMVar_hsa_circ_162435,RMVar_hsa_circ_50113,RMVar_hsa_circ_69082,RMVar_hsa_circ_50689,RMVar_hsa_circ_18692,RMVar_hsa_circ_162446,RMVar_hsa_circ_316874,RMVar_hsa_circ_272147,RMVar_hsa_circ_162455,RMVar_hsa_circ_162456,RMVar_hsa_circ_335720,RMVar_hsa_circ_356413,RMVar_hsa_circ_269928,RMVar_hsa_circ_162457,RMVar_hsa_circ_324082,RMVar_hsa_circ_313867,RMVar_hsa_circ_84604,RMVar_hsa_circ_162469,RMVar_hsa_circ_162470,RMVar_hsa_circ_162468,RMVar_hsa_circ_162471,RMVar_hsa_circ_334895,RMVar_hsa_circ_341678,RMVar_hsa_circ_357735,RMVar_hsa_circ_340753,RMVar_hsa_circ_162476,RMVar_hsa_circ_162477,RMVar_hsa_circ_4669,RMVar_hsa_circ_53889 21131 RMVar_ID_21131 Human_SNP_ID_524978563 A-to-I Human chr13 + 28280060 28280060 28280060 CACCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAAGTGTGAACCACTGCACCTGGCCTGTAACA CACCTGCCTCGGCCTCCCAAAGTGCTGGGATTGCAAGTGTGAACCACTGCACCTGGCCTGTAACA A G PAN3 Ensembl:ENSG00000152520 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1240435690 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8389921 RMVar_hsa_circ_50550,RMVar_hsa_circ_90916,RMVar_hsa_circ_162435,RMVar_hsa_circ_50113,RMVar_hsa_circ_69082,RMVar_hsa_circ_50689,RMVar_hsa_circ_18692,RMVar_hsa_circ_162446,RMVar_hsa_circ_316874,RMVar_hsa_circ_272147,RMVar_hsa_circ_162455,RMVar_hsa_circ_162456,RMVar_hsa_circ_335720,RMVar_hsa_circ_356413,RMVar_hsa_circ_269928,RMVar_hsa_circ_162457,RMVar_hsa_circ_324082,RMVar_hsa_circ_313867,RMVar_hsa_circ_84604,RMVar_hsa_circ_162469,RMVar_hsa_circ_162470,RMVar_hsa_circ_162468,RMVar_hsa_circ_162471,RMVar_hsa_circ_334895,RMVar_hsa_circ_341678,RMVar_hsa_circ_357735,RMVar_hsa_circ_340753,RMVar_hsa_circ_162476,RMVar_hsa_circ_162477,RMVar_hsa_circ_4669,RMVar_hsa_circ_53889 21132 RMVar_ID_21132 Human_SNP_ID_524980991 A-to-I Human chr13 + 28289417 28289417 28289417 TTCCCACCTCAGTCTCCTGAATAGCTGGGACCACAGGCACACGCCACCACACCCAGCTAATTTTT TTCCCACCTCAGTCTCCTGAATAGCTGGGACCGCAGGCACACGCCACCACACCCAGCTAATTTTT A G PAN3 Ensembl:ENSG00000152520 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1372337381 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84604,RMVar_hsa_circ_162470,RMVar_hsa_circ_162478,RMVar_hsa_circ_96116 21133 RMVar_ID_21133 Human_SNP_ID_524981017 A-to-I Human chr13 + 28289478 28289478 28289478 TTTTGTCCTTTTGGTCGATACGGGATTTCACCATGTTGCTCAGGCTGGTCCCAAACTCCTGAGAT TTTTGTCCTTTTGGTCGATACGGGATTTCACCGTGTTGCTCAGGCTGGTCCCAAACTCCTGAGAT A G PAN3 Ensembl:ENSG00000152520 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1017799074 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84604,RMVar_hsa_circ_162470,RMVar_hsa_circ_162478,RMVar_hsa_circ_96116 21134 RMVar_ID_21134 Human_SNP_ID_524981038 A-to-I Human chr13 + 28289544 28289544 28289544 AAGCAGTCCACCCACCCCCAAAGTGTTGGGATAATAGCCGTGAGCCACCACGCCCAGCAGCATTA AAGCAGTCCACCCACCCCCAAAGTGTTGGGATGATAGCCGTGAGCCACCACGCCCAGCAGCATTA A G PAN3 Ensembl:ENSG00000152520 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs945421147 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84604,RMVar_hsa_circ_162470,RMVar_hsa_circ_162478,RMVar_hsa_circ_96116 21135 RMVar_ID_21135 Human_SNP_ID_524981426 A-to-I Human chr13 + 28290614 28290614 28290614 GAGGCAGGAGAATCATTTGAACCCCAGGAGGCAGAGGTTGCAGTGAGCCGAGATTGTGCCATTGT GAGGCAGGAGAATCATTTGAACCCCAGGAGGCGGAGGTTGCAGTGAGCCGAGATTGTGCCATTGT A G PAN3 Ensembl:ENSG00000152520 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs141125090 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84604,RMVar_hsa_circ_162470,RMVar_hsa_circ_162478,RMVar_hsa_circ_96116 21136 RMVar_ID_21136 Human_SNP_ID_525073433 A-to-I Human chr13 + 28669399 28669399 28669399 ATGTTTTTACTTTGTATTTATTTTTTTGATACAGGATCTCATTCTGTCATCCAGGCTGGAGTGCA ATGTTTTTACTTTGTATTTATTTTTTTGATACGGGATCTCATTCTGTCATCCAGGCTGGAGTGCA A G POMP Ensembl:ENSG00000132963 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054310382 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12125888 RMVar_hsa_circ_340962,RMVar_hsa_circ_340781 21137 RMVar_ID_21137 Human_SNP_ID_525074766 A-to-I Human chr13 + 28674932 28674932 28674932 ATAGTGGTGTGCAGCTGTAGTCCCAGGTACTCAGGAGGCTGAGGCAGGAGGATCACTTGAGCCCA ATAGTGGTGTGCAGCTGTAGTCCCAGGTACTCGGGAGGCTGAGGCAGGAGGATCACTTGAGCCCA A G POMP Ensembl:ENSG00000132963 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs912941165 Functional Loss SNV dbSNP153 33..33 33 - - - 21138 RMVar_ID_21138 Human_SNP_ID_525074857 A-to-I Human chr13 + 28675244 28675244 28675244 CTTACTGTAACCTCCACCTCCTGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCAGGTAGCTGGG CTTACTGTAACCTCCACCTCCTGGGTTCAAGCCATTCTCCTGCCTCAGCCTCCCAGGTAGCTGGG A C POMP Ensembl:ENSG00000132963 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs142911190 Functional Loss SNV dbSNP153 33..33 33 - - - 21139 RMVar_ID_21139 Human_SNP_ID_525074858 A-to-I Human chr13 + 28675244 28675244 28675244 CTTACTGTAACCTCCACCTCCTGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCAGGTAGCTGGG CTTACTGTAACCTCCACCTCCTGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAGGTAGCTGGG A G POMP Ensembl:ENSG00000132963 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs142911190 Functional Loss SNV dbSNP153 33..33 33 - - - 21140 RMVar_ID_21140 Human_SNP_ID_525074894 A-to-I Human chr13 + 28675415 28675415 28675415 CCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCATCACGCCCGGCCAGGTAGATG CCCGCCTCAGCCTCCCAAAGTGCTGGGATTACCGGCGTGAGCCATCACGCCCGGCCAGGTAGATG A C POMP Ensembl:ENSG00000132963 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1350812557 Functional Loss SNV dbSNP153 33..33 33 - - - 21141 RMVar_ID_21141 Human_SNP_ID_525347739 A-to-I Human chr13 - 29766775 29766775 29766775 TGGAAGACACTCAGCAATTAATGAAGTTAATTACTGGGCCAACTTGAGAGGAAAAAATGGAAAAG TGGAAGACACTCAGCAATTAATGAAGTTAATTTCTGGGCCAACTTGAGAGGAAAAAATGGAAAAG T A UBL3 Ensembl:ENSG00000122042 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1037456556 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6270025,Human_RBP_ID_18267468 Human_miRNA_ID_2781454,Human_miRNA_ID_2787019 RMVar_hsa_circ_98192,RMVar_hsa_circ_162513 21142 RMVar_ID_21142 Human_SNP_ID_525347740 A-to-I Human chr13 - 29766775 29766775 29766775 TGGAAGACACTCAGCAATTAATGAAGTTAATTACTGGGCCAACTTGAGAGGAAAAAATGGAAAAG TGGAAGACACTCAGCAATTAATGAAGTTAATTGCTGGGCCAACTTGAGAGGAAAAAATGGAAAAG T C UBL3 Ensembl:ENSG00000122042 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1037456556 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6270025,Human_RBP_ID_18267468 Human_miRNA_ID_2781454,Human_miRNA_ID_2787019 RMVar_hsa_circ_98192,RMVar_hsa_circ_162513 21143 RMVar_ID_21143 Human_SNP_ID_147111831 A-to-I Human chr3 + 105374294 105374294 105374294 ACCTAATTCTGGGGCCAGGCTCAGTGGCTCATACCTATAATCCTAGCACTTTGGGAGGCCGAGGC ACCTAATTCTGGGGCCAGGCTCAGTGGCTCATGCCTATAATCCTAGCACTTTGGGAGGCCGAGGC A G ALCAM Ensembl:ENSG00000170017 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1036910964 Functional Loss SNV dbSNP153 33..33 33 - - - 21144 RMVar_ID_21144 Human_SNP_ID_147111833 A-to-I Human chr3 + 105374298 105374298 105374298 AATTCTGGGGCCAGGCTCAGTGGCTCATACCTATAATCCTAGCACTTTGGGAGGCCGAGGCGGGC AATTCTGGGGCCAGGCTCAGTGGCTCATACCTGTAATCCTAGCACTTTGGGAGGCCGAGGCGGGC A G ALCAM Ensembl:ENSG00000170017 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs898086849 Functional Loss SNV dbSNP153 33..33 33 - - - 21145 RMVar_ID_21145 Human_SNP_ID_147158441 A-to-I Human chr3 + 105576495 105576495 105576495 CAGAAAGAAGCAACATGACAATAGAGAGAGTTATGCTACAATTATTTCTTGGTTTCCACTTGCAA CAGAAAGAAGCAACATGACAATAGAGAGAGTTGTGCTACAATTATTTCTTGGTTTCCACTTGCAA A G ALCAM Ensembl:ENSG00000170017 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1191808027 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_584835 RMVar_hsa_circ_220139,RMVar_hsa_circ_88729 21146 RMVar_ID_21146 Human_SNP_ID_147180441 A-to-I Human chr3 - 105660970 105660966 105660970 AATGAGACTTCATCTCATTTAAAAAAAAAAAAAAAAGAAGAAGACATCCTATTTGATGTGGAAAC AATGAGACTTCATCTCATTTAAAAAAAAAAAA____GAAGAAGACATCCTATTTGATGTGGAAAC CTTTT C CBLB Ensembl:ENSG00000114423 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs35803625 Functional Loss DEL dbSNP153 33..36 33 - - - 21147 RMVar_ID_21147 Human_SNP_ID_147180442 A-to-I Human chr3 - 105660970 105660966 105660970 AATGAGACTTCATCTCATTTAAAAAAAAAAAAAAAAGAAGAAGACATCCTATTTGATGTGGAAAC AATGAGACTTCATCTCATTTAAAAAAAAAAAA___AGAAGAAGACATCCTATTTGATGTGGAAAC CTTTT CT CBLB Ensembl:ENSG00000114423 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs35803625 Functional Loss DEL dbSNP153 33..35 33 - - - 21148 RMVar_ID_21148 Human_SNP_ID_147180443 A-to-I Human chr3 - 105660970 105660966 105660970 AATGAGACTTCATCTCATTTAAAAAAAAAAAAAAAAGAAGAAGACATCCTATTTGATGTGGAAAC AATGAGACTTCATCTCATTTAAAAAAAAAAAA__AAGAAGAAGACATCCTATTTGATGTGGAAAC CTTTT CTT CBLB Ensembl:ENSG00000114423 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs35803625 Functional Loss DEL dbSNP153 33..34 33 - - - 21149 RMVar_ID_21149 Human_SNP_ID_147180444 A-to-I Human chr3 - 105660970 105660966 105660970 AATGAGACTTCATCTCATTTAAAAAAAAAAAAAAAAGAAGAAGACATCCTATTTGATGTGGAAAC AATGAGACTTCATCTCATTTAAAAAAAAAAAA_AAAGAAGAAGACATCCTATTTGATGTGGAAAC CTTTT CTTT CBLB Ensembl:ENSG00000114423 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs35803625 Functional Loss DEL dbSNP153 33..33 33 - - - 21150 RMVar_ID_21150 Human_SNP_ID_147225976 A-to-I Human chr3 - 105848958 105848958 105848958 TATGAAAATCTGTACATTACCAATCAGAACCTAAAAGTCTCCCATGAAATGTTTCTACATAAGCA TATGAAAATCTGTACATTACCAATCAGAACCTGAAAGTCTCCCATGAAATGTTTCTACATAAGCA T C CBLB Ensembl:ENSG00000114423 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251598562 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55131,RMVar_hsa_circ_264787,RMVar_hsa_circ_342428,RMVar_hsa_circ_299859,RMVar_hsa_circ_220161,RMVar_hsa_circ_220162,RMVar_hsa_circ_363072 21151 RMVar_ID_21151 Human_SNP_ID_147225985 A-to-I Human chr3 - 105848983 105848983 105848983 GTCAGCATTATGAGATCTATTGATCTATGAAAATCTGTACATTACCAATCAGAACCTAAAAGTCT GTCAGCATTATGAGATCTATTGATCTATGAAAGTCTGTACATTACCAATCAGAACCTAAAAGTCT T C CBLB Ensembl:ENSG00000114423 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs749600752 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55131,RMVar_hsa_circ_264787,RMVar_hsa_circ_342428,RMVar_hsa_circ_299859,RMVar_hsa_circ_220161,RMVar_hsa_circ_220162,RMVar_hsa_circ_363072 21152 RMVar_ID_21152 Human_SNP_ID_147225989 A-to-I Human chr3 - 105848997 105848997 105848997 CCTCATTCTGAATAGTCAGCATTATGAGATCTATTGATCTATGAAAATCTGTACATTACCAATCA CCTCATTCTGAATAGTCAGCATTATGAGATCTGTTGATCTATGAAAATCTGTACATTACCAATCA T C CBLB Ensembl:ENSG00000114423 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs931742966 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55131,RMVar_hsa_circ_264787,RMVar_hsa_circ_342428,RMVar_hsa_circ_299859,RMVar_hsa_circ_220161,RMVar_hsa_circ_220162,RMVar_hsa_circ_363072 21153 RMVar_ID_21153 Human_SNP_ID_147226112 A-to-I Human chr3 - 105849539 105849538 105849540 CTTATGTGGAAACATTTCATGGGAGACATTTAAGTTTTGTTTGATAATGTATAGATTCCCATAGA CTTATGTGGAAACATTTCATGGGAGACATTT__GTTTTGTTTGATAATGTATAGATTCCCATAGA CTT C CBLB Ensembl:ENSG00000114423 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1161823881 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_55131,RMVar_hsa_circ_264787,RMVar_hsa_circ_342428,RMVar_hsa_circ_299859,RMVar_hsa_circ_220161,RMVar_hsa_circ_220162,RMVar_hsa_circ_363072 21154 RMVar_ID_21154 Human_SNP_ID_147226112 A-to-I Human chr3 - 105849540 105849538 105849540 GCTTATGTGGAAACATTTCATGGGAGACATTTAAGTTTTGTTTGATAATGTATAGATTCCCATAG GCTTATGTGGAAACATTTCATGGGAGACATTT__GTTTTGTTTGATAATGTATAGATTCCCATAG CTT C CBLB Ensembl:ENSG00000114423 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1161823881 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_55131,RMVar_hsa_circ_264787,RMVar_hsa_circ_342428,RMVar_hsa_circ_299859,RMVar_hsa_circ_220161,RMVar_hsa_circ_220162,RMVar_hsa_circ_363072 21155 RMVar_ID_21155 Human_SNP_ID_147428446 A-to-I Human chr3 - 106651311 106651311 106651311 TGAATCCGGGAGGCGGAGGTTGCTGTGGGCCGAGATCGCGCCACTGCACTCCAGCCTAGGCTACA TGAATCCGGGAGGCGGAGGTTGCTGTGGGCCGTGATCGCGCCACTGCACTCCAGCCTAGGCTACA T A LINC00882 Ensembl:ENSG00000242759 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1291010187 Functional Loss SNV dbSNP153 33..33 33 - - - 21156 RMVar_ID_21156 Human_SNP_ID_147569835 A-to-I Human chr3 + 107245247 107245247 107245247 TCAAGTAATTCTCCTGCTTCAGCCTCCTGAGTAGCTAGGATTACAGGCATGCACCATCATACCTG TCAAGTAATTCTCCTGCTTCAGCCTCCTGAGTGGCTAGGATTACAGGCATGCACCATCATACCTG A G DUBR Ensembl:ENSG00000243701 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1311941579 Functional Loss SNV dbSNP153 33..33 33 - - - 21157 RMVar_ID_21157 Human_SNP_ID_147571049 A-to-I Human chr3 + 107250962 107250962 107250962 GCAATCTCGGCTCACTGCAGCCTCTGCCTCCCAGGCTCAAGCAATTATCCTGCCTCAGCCTCCCG GCAATCTCGGCTCACTGCAGCCTCTGCCTCCCCGGCTCAAGCAATTATCCTGCCTCAGCCTCCCG A C DUBR Ensembl:ENSG00000243701 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1264033948 Functional Loss SNV dbSNP153 33..33 33 - - - 21158 RMVar_ID_21158 Human_SNP_ID_147571052 A-to-I Human chr3 + 107250972 107250972 107250972 CTCACTGCAGCCTCTGCCTCCCAGGCTCAAGCAATTATCCTGCCTCAGCCTCCCGAGTAGCTGGG CTCACTGCAGCCTCTGCCTCCCAGGCTCAAGCGATTATCCTGCCTCAGCCTCCCGAGTAGCTGGG A G DUBR Ensembl:ENSG00000243701 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1430330809 Functional Loss SNV dbSNP153 33..33 33 - - - 21159 RMVar_ID_21159 Human_SNP_ID_147571478 A-to-I Human chr3 + 107252810 107252809 107252810 CCCGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAAATTAGCTGGGCGTGGTGGCA CCCGGCCAACATGGTGAAACCCCATCTCTACT_AAAATACAAAAAATTAGCTGGGCGTGGTGGCA TA T DUBR Ensembl:ENSG00000243701 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1192115982 Functional Loss DEL dbSNP153 33..33 33 - - - 21160 RMVar_ID_21160 Human_SNP_ID_147642253 A-to-I Human chr3 + 107559762 107559762 107559762 TTAGGATTAGAATTCTGTTTTGTTTTTTCTTTAAACAGATTCTCGCTCTGTCACCCTGGCTGGAG TTAGGATTAGAATTCTGTTTTGTTTTTTCTTTGAACAGATTCTCGCTCTGTCACCCTGGCTGGAG A G BBX Ensembl:ENSG00000114439 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1175603236 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2731663 RMVar_hsa_circ_85695,RMVar_hsa_circ_486,RMVar_hsa_circ_220174,RMVar_hsa_circ_370388,RMVar_hsa_circ_220175 21161 RMVar_ID_21161 Human_SNP_ID_147642306 A-to-I Human chr3 + 107559987 107559987 107559987 GCTGGTCTCGAACTTCTGGGCTCAAGCAATCCACCCACCTTGGTCTCCCAAAATGCTGGCATTAT GCTGGTCTCGAACTTCTGGGCTCAAGCAATCCGCCCACCTTGGTCTCCCAAAATGCTGGCATTAT A G BBX Ensembl:ENSG00000114439 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1303552181 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85695,RMVar_hsa_circ_486,RMVar_hsa_circ_220174,RMVar_hsa_circ_370388,RMVar_hsa_circ_220175 21162 RMVar_ID_21162 Human_SNP_ID_147645729 A-to-I Human chr3 + 107573925 107573925 107573925 ATTTTGTATTAGCCGGGAGACCGGGTTTCTCCATGTTGGTCAGGCTGCTCTCAAACTCCTGATCT ATTTTGTATTAGCCGGGAGACCGGGTTTCTCCCTGTTGGTCAGGCTGCTCTCAAACTCCTGATCT A C BBX Ensembl:ENSG00000114439 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs865836565 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85695,RMVar_hsa_circ_486,RMVar_hsa_circ_220174,RMVar_hsa_circ_370388,RMVar_hsa_circ_220175 21163 RMVar_ID_21163 Human_SNP_ID_147645730 A-to-I Human chr3 + 107573925 107573925 107573925 ATTTTGTATTAGCCGGGAGACCGGGTTTCTCCATGTTGGTCAGGCTGCTCTCAAACTCCTGATCT ATTTTGTATTAGCCGGGAGACCGGGTTTCTCCGTGTTGGTCAGGCTGCTCTCAAACTCCTGATCT A G BBX Ensembl:ENSG00000114439 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs865836565 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85695,RMVar_hsa_circ_486,RMVar_hsa_circ_220174,RMVar_hsa_circ_370388,RMVar_hsa_circ_220175 21164 RMVar_ID_21164 Human_SNP_ID_147649107 A-to-I Human chr3 + 107587215 107587215 107587215 AAAAATTAGCTGTTGTGGTGGTTCATGCCAGCAATCCCAGCTACTTTGCAGCTACTTTGGTAGCT AAAAATTAGCTGTTGTGGTGGTTCATGCCAGCCATCCCAGCTACTTTGCAGCTACTTTGGTAGCT A C BBX Ensembl:ENSG00000114439 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs888078811 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85695,RMVar_hsa_circ_486,RMVar_hsa_circ_220174,RMVar_hsa_circ_370388,RMVar_hsa_circ_220175 21165 RMVar_ID_21165 Human_SNP_ID_147756851 A-to-I Human chr3 - 108043576 108043576 108043576 CCATTCTAAATAAAGAGAACTCCAGTGTTGCTATGTGCAAGATCCTCTCTTGGAGCTTTTTTGCA CCATTCTAAATAAAGAGAACTCCAGTGTTGCTCTGTGCAAGATCCTCTCTTGGAGCTTTTTTGCA T G CD47 Ensembl:ENSG00000196776 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs548547393 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14560763,Human_RBP_ID_18331090,Human_RBP_ID_27709944 Human_miRNA_ID_1141787,Human_miRNA_ID_1375665 21166 RMVar_ID_21166 Human_SNP_ID_147757486 A-to-I Human chr3 - 108046492 108046492 108046492 GTAGCACCTTTTCTCCTCTTTGAACATGGTCTAGTGACACGGTAGCACCAGTTGCAGGAAGGAGC GTAGCACCTTTTCTCCTCTTTGAACATGGTCTGGTGACACGGTAGCACCAGTTGCAGGAAGGAGC T C CD47 Ensembl:ENSG00000196776 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1056927070 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_585053,Human_RBP_ID_1104541,Human_RBP_ID_3680999,Human_RBP_ID_9129150,Human_RBP_ID_14560804,Human_RBP_ID_17702472,Human_RBP_ID_20793173,Human_RBP_ID_22397074,Human_RBP_ID_23957852 Human_miRNA_ID_721001 21167 RMVar_ID_21167 Human_SNP_ID_147758474 A-to-I Human chr3 - 108050344 108050343 108050345 TGGGAGGCCAAGGCGGGCAGATCACGAGGTCAAGAGATTGAGACCATCCTGGCCAACATGTTGAA TGGGAGGCCAAGGCGGGCAGATCACGAGGTC__GAGATTGAGACCATCCTGGCCAACATGTTGAA CTT C CD47 Ensembl:ENSG00000196776 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1306098465 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_13659,RMVar_hsa_circ_29199 21168 RMVar_ID_21168 Human_SNP_ID_147909613 A-to-I Human chr3 + 108691457 108691457 108691457 GTGGATATTCACGGAGAGCTATGAGGGGATAAAAGGGTATGATCTAATGGTAAGAAACTGGAAGA GTGGATATTCACGGAGAGCTATGAGGGGATAAGAGGGTATGATCTAATGGTAAGAAACTGGAAGA A G DZIP3 Ensembl:ENSG00000198919 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1218837117 Functional Loss SNV dbSNP153 33..33 33 - - - 21169 RMVar_ID_21169 Human_SNP_ID_148485736 A-to-I Human chr3 - 111067421 111067421 111067421 TGAGCCAAGATTGCATCCCTGTACTCTAGCCTAGGCAGCTGGAGAAAGACCCTGTCCCCCAAAAA TGAGCCAAGATTGCATCCCTGTACTCTAGCCTGGGCAGCTGGAGAAAGACCCTGTCCCCCAAAAA T C NECTIN3-AS1 Ensembl:ENSG00000242242 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs951131270 Functional Loss SNV dbSNP153 33..33 33 - - - 21170 RMVar_ID_21170 Human_SNP_ID_148683526 A-to-I Human chr3 + 111896205 111896205 111896205 GAACTCCTGGCCTCAAGTGATTTGCTCCCCTTAGCCTCTGAAACTATTGGGATTACAGGCGTGAG GAACTCCTGGCCTCAAGTGATTTGCTCCCCTTTGCCTCTGAAACTATTGGGATTACAGGCGTGAG A T PHLDB2 Ensembl:ENSG00000144824 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs779227121 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45973,RMVar_hsa_circ_58960,RMVar_hsa_circ_66165,RMVar_hsa_circ_376745,RMVar_hsa_circ_48416 21171 RMVar_ID_21171 Human_SNP_ID_148687452 A-to-I Human chr3 + 111913374 111913374 111913374 CCTCAGTCTCTGTGCTGAATACACAAAGCCTGACAGTCGCTTATCTACTGGGACCACCGTGGAAG CCTCAGTCTCTGTGCTGAATACACAAAGCCTGGCAGTCGCTTATCTACTGGGACCACCGTGGAAG A G PHLDB2 Ensembl:ENSG00000144824 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs773164528 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_67790,Human_RBP_ID_5601803,Human_RBP_ID_9393915 Human_Splice_Rec_466514,Human_Splice_Rec_466546,Human_Splice_Rec_466578,Human_Splice_Rec_466612,Human_Splice_Rec_466642,Human_Splice_Rec_466646,Human_Splice_Rec_466678,Human_Splice_Rec_466708,Human_Splice_Rec_466728 RMVar_hsa_circ_220261,RMVar_hsa_circ_45973,RMVar_hsa_circ_58960,RMVar_hsa_circ_66165,RMVar_hsa_circ_376745,RMVar_hsa_circ_48416,RMVar_hsa_circ_113502,RMVar_hsa_circ_121506,RMVar_hsa_circ_220262,RMVar_hsa_circ_220264,RMVar_hsa_circ_220268,RMVar_hsa_circ_337064,RMVar_hsa_circ_350116,RMVar_hsa_circ_354119,RMVar_hsa_circ_359240,RMVar_hsa_circ_352759,RMVar_hsa_circ_347627,RMVar_hsa_circ_281349,RMVar_hsa_circ_298849,RMVar_hsa_circ_118216,RMVar_hsa_circ_220266,RMVar_hsa_circ_220267,RMVar_hsa_circ_220265,RMVar_hsa_circ_220263 21172 RMVar_ID_21172 Human_SNP_ID_148691028 A-to-I Human chr3 + 111929004 111929004 111929004 GCATTTTAGGCTAGGTGCAGTGGCTCATGCCTATAATCCCAGCACTTTAGGAGGCCGAAGTGGGA GCATTTTAGGCTAGGTGCAGTGGCTCATGCCTGTAATCCCAGCACTTTAGGAGGCCGAAGTGGGA A G PHLDB2 Ensembl:ENSG00000144824 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1381340987 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45973,RMVar_hsa_circ_376745,RMVar_hsa_circ_220268,RMVar_hsa_circ_337064,RMVar_hsa_circ_350116,RMVar_hsa_circ_354119,RMVar_hsa_circ_359240,RMVar_hsa_circ_352759,RMVar_hsa_circ_347627,RMVar_hsa_circ_118216,RMVar_hsa_circ_220266,RMVar_hsa_circ_220267,RMVar_hsa_circ_220265,RMVar_hsa_circ_70567,RMVar_hsa_circ_74564,RMVar_hsa_circ_354869,RMVar_hsa_circ_365772,RMVar_hsa_circ_365378,RMVar_hsa_circ_74532,RMVar_hsa_circ_54778,RMVar_hsa_circ_50600 21173 RMVar_ID_21173 Human_SNP_ID_148697158 A-to-I Human chr3 + 111955530 111955529 111955530 GAATGCAGTGGTGTGTGATTATAGCTCACTGCAAACTCTGCCACCTGGGTTCAAGTGATCCTCCC GAATGCAGTGGTGTGTGATTATAGCTCACTGC_AACTCTGCCACCTGGGTTCAAGTGATCCTCCC CA C PHLDB2 Ensembl:ENSG00000144824 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1397840891 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_2732983 RMVar_hsa_circ_220268,RMVar_hsa_circ_118216,RMVar_hsa_circ_74532,RMVar_hsa_circ_120442,RMVar_hsa_circ_220269,RMVar_hsa_circ_323584,RMVar_hsa_circ_220272,RMVar_hsa_circ_312051,RMVar_hsa_circ_220274,RMVar_hsa_circ_332219,RMVar_hsa_circ_280663,RMVar_hsa_circ_361176 21174 RMVar_ID_21174 Human_SNP_ID_148697159 A-to-I Human chr3 + 111955530 111955530 111955530 GAATGCAGTGGTGTGTGATTATAGCTCACTGCAAACTCTGCCACCTGGGTTCAAGTGATCCTCCC GAATGCAGTGGTGTGTGATTATAGCTCACTGCCAACTCTGCCACCTGGGTTCAAGTGATCCTCCC A C PHLDB2 Ensembl:ENSG00000144824 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1464942180 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2732983 RMVar_hsa_circ_220268,RMVar_hsa_circ_118216,RMVar_hsa_circ_74532,RMVar_hsa_circ_120442,RMVar_hsa_circ_220269,RMVar_hsa_circ_323584,RMVar_hsa_circ_220272,RMVar_hsa_circ_312051,RMVar_hsa_circ_220274,RMVar_hsa_circ_332219,RMVar_hsa_circ_280663,RMVar_hsa_circ_361176 21175 RMVar_ID_21175 Human_SNP_ID_148697160 A-to-I Human chr3 + 111955530 111955530 111955530 GAATGCAGTGGTGTGTGATTATAGCTCACTGCAAACTCTGCCACCTGGGTTCAAGTGATCCTCCC GAATGCAGTGGTGTGTGATTATAGCTCACTGCGAACTCTGCCACCTGGGTTCAAGTGATCCTCCC A G PHLDB2 Ensembl:ENSG00000144824 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1464942180 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2732983 RMVar_hsa_circ_220268,RMVar_hsa_circ_118216,RMVar_hsa_circ_74532,RMVar_hsa_circ_120442,RMVar_hsa_circ_220269,RMVar_hsa_circ_323584,RMVar_hsa_circ_220272,RMVar_hsa_circ_312051,RMVar_hsa_circ_220274,RMVar_hsa_circ_332219,RMVar_hsa_circ_280663,RMVar_hsa_circ_361176 21176 RMVar_ID_21176 Human_SNP_ID_148826143 A-to-I Human chr3 - 112488030 112488030 112488030 AGACATTTTCCATCCTGAATCAATTGAACTTCATGGCTGATGGAATGGGACGGTGACAAGGAAGG AGACATTTTCCATCCTGAATCAATTGAACTTCTTGGCTGATGGAATGGGACGGTGACAAGGAAGG T A BTLA Ensembl:ENSG00000186265 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2633554 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_220292,RMVar_hsa_circ_88488 21177 RMVar_ID_21177 Human_SNP_ID_148826144 A-to-I Human chr3 - 112488030 112488030 112488030 AGACATTTTCCATCCTGAATCAATTGAACTTCATGGCTGATGGAATGGGACGGTGACAAGGAAGG AGACATTTTCCATCCTGAATCAATTGAACTTCGTGGCTGATGGAATGGGACGGTGACAAGGAAGG T C BTLA Ensembl:ENSG00000186265 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2633554 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_220292,RMVar_hsa_circ_88488 21178 RMVar_ID_21178 Human_SNP_ID_148827328 A-to-I Human chr3 - 112493597 112493597 112493597 CTTGGGAGGCTGAGGCAGAATTGCTTGAACCCAGGAGACTGAAGTTGCAGTGAGCCAGGTTGCAC CTTGGGAGGCTGAGGCAGAATTGCTTGAACCCGGGAGACTGAAGTTGCAGTGAGCCAGGTTGCAC T C BTLA Ensembl:ENSG00000186265 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1363841157 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_220292,RMVar_hsa_circ_88488 21179 RMVar_ID_21179 Human_SNP_ID_148827339 A-to-I Human chr3 - 112493648 112493648 112493648 AAAATACAAAAATTAGCTGGGCGTGGTGGGACACGCCTGTAAGACCAGCTACTTGGGAGGCTGAG AAAATACAAAAATTAGCTGGGCGTGGTGGGACTCGCCTGTAAGACCAGCTACTTGGGAGGCTGAG T A BTLA Ensembl:ENSG00000186265 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs374392802 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_220292,RMVar_hsa_circ_88488 21180 RMVar_ID_21180 Human_SNP_ID_148827359 A-to-I Human chr3 - 112493706 112493706 112493706 TTTGAGGTCAGGAGTTCAAGAGCAGTCTGGCCAGCATAGTGAAACCCTGTCTGTACTAAAAATAC TTTGAGGTCAGGAGTTCAAGAGCAGTCTGGCCGGCATAGTGAAACCCTGTCTGTACTAAAAATAC T C BTLA Ensembl:ENSG00000186265 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1400901921 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_220292,RMVar_hsa_circ_88488 21181 RMVar_ID_21181 Human_SNP_ID_148827368 A-to-I Human chr3 - 112493775 112493775 112493775 TGTTTAGGCTGGGTGTAGTGGCTCTCGCCTGTAATCCCAGCACTTCAGGAAGCTGAGGAGGGCGG TGTTTAGGCTGGGTGTAGTGGCTCTCGCCTGTGATCCCAGCACTTCAGGAAGCTGAGGAGGGCGG T C BTLA Ensembl:ENSG00000186265 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1361366933 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_220292,RMVar_hsa_circ_88488 21182 RMVar_ID_21182 Human_SNP_ID_148828258 A-to-I Human chr3 - 112497949 112497949 112497949 GAGCTCCTGACCTCAAGTGATCCACCTGCCTCAGCCTCCCAAAGTGCTAGGATTACAGGTATGAG GAGCTCCTGACCTCAAGTGATCCACCTGCCTCTGCCTCCCAAAGTGCTAGGATTACAGGTATGAG T A BTLA Ensembl:ENSG00000186265 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs934701174 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_220292,RMVar_hsa_circ_88488 21183 RMVar_ID_21183 Human_SNP_ID_148828285 A-to-I Human chr3 - 112498074 112498074 112498074 AGTAGTGATAGATTTGTACTTAACTATTTATAACATCTACTCAGTTCTCTTTTCTTGCCATCAAC AGTAGTGATAGATTTGTACTTAACTATTTATAGCATCTACTCAGTTCTCTTTTCTTGCCATCAAC T C BTLA Ensembl:ENSG00000186265 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1163651225 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_220292,RMVar_hsa_circ_88488 21184 RMVar_ID_21184 Human_SNP_ID_148828308 A-to-I Human chr3 - 112498149 112498149 112498149 CTCTACTGCACTCAGTTTGGGAAGAACGAGCTATCTATTCATCATCAGTGTGGCAGCCTGAGCAT CTCTACTGCACTCAGTTTGGGAAGAACGAGCTGTCTATTCATCATCAGTGTGGCAGCCTGAGCAT T C BTLA Ensembl:ENSG00000186265 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs560363320 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_220292,RMVar_hsa_circ_88488 21185 RMVar_ID_21185 Human_SNP_ID_148828538 A-to-I Human chr3 - 112498906 112498906 112498906 ACTGATAATGAATAGATAGCTCGTTCTTTCCAAACTGAGTGCAGTAGAGTGCTGCAGTGCTCAGT ACTGATAATGAATAGATAGCTCGTTCTTTCCACACTGAGTGCAGTAGAGTGCTGCAGTGCTCAGT T G BTLA Ensembl:ENSG00000186265 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1225771278 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_220292,RMVar_hsa_circ_88488 21186 RMVar_ID_21186 Human_SNP_ID_148843016 A-to-I Human chr3 - 112557254 112557252 112557254 AGGAGGCAGAGGCAGGCGGAATACAGGCTAACAGGGCGAAACCCCGTCTCTACTAAAAATATAAA AGGAGGCAGAGGCAGGCGGAATACAGGCTAAC__GGCGAAACCCCGTCTCTACTAAAAATATAAA CCT C ATG3 Ensembl:ENSG00000144848 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1333310201 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_115532,RMVar_hsa_circ_22823,RMVar_hsa_circ_220293,RMVar_hsa_circ_90620,RMVar_hsa_circ_341582,RMVar_hsa_circ_220295,RMVar_hsa_circ_345803,RMVar_hsa_circ_220299,RMVar_hsa_circ_220300,RMVar_hsa_circ_319898 21187 RMVar_ID_21187 Human_SNP_ID_148846157 A-to-I Human chr3 + 112567585 112567585 112567585 CCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGCACCCAGCTAGAAGGGAGGGTT CCTCGGCCTCCCAAAGTGCTGGGATTACAGGCCTGAGCCACTGCACCCAGCTAGAAGGGAGGGTT A C SLC35A5 Ensembl:ENSG00000138459 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1033346050 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_281184,RMVar_hsa_circ_299875,RMVar_hsa_circ_220301 21188 RMVar_ID_21188 Human_SNP_ID_148846158 A-to-I Human chr3 + 112567585 112567585 112567585 CCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGCACCCAGCTAGAAGGGAGGGTT CCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCACCCAGCTAGAAGGGAGGGTT A G SLC35A5 Ensembl:ENSG00000138459 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1033346050 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_281184,RMVar_hsa_circ_299875,RMVar_hsa_circ_220301 21189 RMVar_ID_21189 Human_SNP_ID_148855601 A-to-I Human chr3 - 112605109 112605109 112605109 GAAGGACCTTATTTGGCATATAAAATTTTATAAAATATGTATTTAAAGCTTTTTCTTATTTTTTG GAAGGACCTTATTTGGCATATAAAATTTTATACAATATGTATTTAAAGCTTTTTCTTATTTTTTG T G CCDC80 Ensembl:ENSG00000091986 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs940912019 Functional Loss SNV dbSNP153 33..33 33 - - - 21190 RMVar_ID_21190 Human_SNP_ID_148948124 A-to-I Human chr3 - 113004347 113004347 113004347 AGACTTTTTGAGAATCACCTGGTGGGTTGCTAAAAGATGCAGATTAGCCCTTTCCCAGAGACTGA AGACTTTTTGAGAATCACCTGGTGGGTTGCTACAAGATGCAGATTAGCCCTTTCCCAGAGACTGA T G NEPRO Ensembl:ENSG00000163608 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs891736355 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_585801 RMVar_hsa_circ_94239,RMVar_hsa_circ_269506,RMVar_hsa_circ_220304 21191 RMVar_ID_21191 Human_SNP_ID_149033954 A-to-I Human chr3 - 113362714 113362714 113362714 CCGATTTGATCTTTTGCTGCAAGCAGACTGGTATTGCTATCGGAAGACTGTGTGAAAAATGTGAT CCGATTTGATCTTTTGCTGCAAGCAGACTGGTGTTGCTATCGGAAGACTGTGTGAAAAATGTGAT T C AC112128.1,CFAP44 Ensembl:ENSG00000285943,Ensembl:ENSG00000206530 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs907035984 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4759695 RMVar_hsa_circ_17148,RMVar_hsa_circ_54588,RMVar_hsa_circ_64270,RMVar_hsa_circ_54740,RMVar_hsa_circ_58011,RMVar_hsa_circ_337524,RMVar_hsa_circ_73770,RMVar_hsa_circ_52860,RMVar_hsa_circ_61391,RMVar_hsa_circ_220311,RMVar_hsa_circ_65789,RMVar_hsa_circ_367192,RMVar_hsa_circ_57895,RMVar_hsa_circ_55815,RMVar_hsa_circ_357973,RMVar_hsa_circ_362066,RMVar_hsa_circ_366459,RMVar_hsa_circ_337267,RMVar_hsa_circ_283390,RMVar_hsa_circ_283663,RMVar_hsa_circ_65354,RMVar_hsa_circ_220315 21192 RMVar_ID_21192 Human_SNP_ID_149054767 A-to-I Human chr3 - 113453568 113453568 113453568 ACACGAATTGCTGATTTGACATTGCAGAATTCAGCTATCAAGGCACATATGAATAATATTATTGA ACACGAATTGCTGATTTGACATTGCAGAATTCGGCTATCAAGGCACATATGAATAATATTATTGA T C AC112128.1,SPICE1 Ensembl:ENSG00000285943,Ensembl:ENSG00000163611 Protein coding,Protein coding CDS,CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs757656889 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1946293,Human_RBP_ID_14566748 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 21193 RMVar_ID_21193 Human_SNP_ID_149058522 A-to-I Human chr3 - 113468819 113468819 113468819 AGCCTGAAGAATCTACTGAGACTCTAGACTCAAGCTACGTTGTGGGACACGTGCTGAACTCAAGG AGCCTGAAGAATCTACTGAGACTCTAGACTCACGCTACGTTGTGGGACACGTGCTGAACTCAAGG T G AC112128.1,SPICE1 Ensembl:ENSG00000285943,Ensembl:ENSG00000163611 Protein coding,Protein coding CDS,CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1300009659 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1946306,Human_RBP_ID_5530608,Human_RBP_ID_9393925,Human_RBP_ID_14566827,Human_RBP_ID_18793888,Human_RBP_ID_19012823 Human_Splice_Rec_468484,Human_Splice_Rec_468485,Human_Splice_Rec_468584,Human_Splice_Rec_468585,Human_Splice_Rec_468606,Human_Splice_Rec_468607,Human_Splice_Rec_468620,Human_Splice_Rec_468621 RMVar_hsa_circ_5064,RMVar_hsa_circ_64525,RMVar_hsa_circ_356254,RMVar_hsa_circ_33696,RMVar_hsa_circ_40568,RMVar_hsa_circ_62995,RMVar_hsa_circ_364674,RMVar_hsa_circ_265854,RMVar_hsa_circ_43525 21194 RMVar_ID_21194 Human_SNP_ID_149092578 A-to-I Human chr3 + 113605268 113605268 113605268 CCTCAGCCTCCCGAGTAGCTGGGATTACAGGCATGTGCCACCATGCCCAGCTAATTTTTTGTGTA CCTCAGCCTCCCGAGTAGCTGGGATTACAGGCGTGTGCCACCATGCCCAGCTAATTTTTTGTGTA A G SIDT1 Ensembl:ENSG00000072858 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs774524742 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_364271,RMVar_hsa_circ_220335,RMVar_hsa_circ_376474,RMVar_hsa_circ_80822,RMVar_hsa_circ_220336 21195 RMVar_ID_21195 Human_SNP_ID_149092714 A-to-I Human chr3 + 113605842 113605842 113605842 CCTGGGCAACATGGCGAAACCCTGACTCTACCAAAAATACAAAAAAATTAGCTGAGTGGTGGCAC CCTGGGCAACATGGCGAAACCCTGACTCTACCGAAAATACAAAAAAATTAGCTGAGTGGTGGCAC A G SIDT1 Ensembl:ENSG00000072858 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1229338928 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_364271,RMVar_hsa_circ_220335,RMVar_hsa_circ_376474,RMVar_hsa_circ_80822,RMVar_hsa_circ_220336 21196 RMVar_ID_21196 Human_SNP_ID_149092747 A-to-I Human chr3 + 113605961 113605961 113605961 GTGGAGGTGTAGATTGCAGTAAGCTGACACTGAGCCACTGCACTCCAGCCTGAGTGACAGAGTGA GTGGAGGTGTAGATTGCAGTAAGCTGACACTGCGCCACTGCACTCCAGCCTGAGTGACAGAGTGA A C SIDT1 Ensembl:ENSG00000072858 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs78134078 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_364271,RMVar_hsa_circ_220335,RMVar_hsa_circ_376474,RMVar_hsa_circ_80822,RMVar_hsa_circ_220336 21197 RMVar_ID_21197 Human_SNP_ID_149119016 A-to-I Human chr3 - 113713553 113713551 113713554 ATACTTAAAATATATTTTTATTAATACTTAATAAAAATATTTTTTAAGTATATGTTACAGATAAA ATACTTAAAATATATTTTTATTAATACTTAA___AAATATTTTTTAAGTATATGTTACAGATAAA TTTA T lnc-NAA50-2 RNACentral:URS00008BD914 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1441058149 Functional Loss DEL dbSNP153 32..34 33 - - - 21198 RMVar_ID_21198 Human_SNP_ID_149119101 A-to-I Human chr3 - 113713801 113713801 113713801 GGGAGGCTAAGGCAGGAGAACTGCTTGAACCCAGGAAGCAGAGGTTGCACTCCAGCCTGGGCAAC GGGAGGCTAAGGCAGGAGAACTGCTTGAACCCGGGAAGCAGAGGTTGCACTCCAGCCTGGGCAAC T C lnc-NAA50-2 RNACentral:URS00008BD914 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1164157950 Functional Loss SNV dbSNP153 33..33 33 - - - 21199 RMVar_ID_21199 Human_SNP_ID_149119256 A-to-I Human chr3 - 113714375 113714375 113714375 ATACAAAAAATTGGCCGGGCGCAGTGGCAGGCACCTGTAGTCCCAGCTACTCGGGAGGCTGAGGC ATACAAAAAATTGGCCGGGCGCAGTGGCAGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs950460825 Functional Loss SNV dbSNP153 33..33 33 - - - 21200 RMVar_ID_21200 Human_SNP_ID_149119272 A-to-I Human chr3 - 113714408 113714408 113714408 GGCTAACACGGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTGGCCGGGCGCAGTGGCAGGC GGCTAACACGGTGAAACCCCGTCTCTACTAAAGATACAAAAAATTGGCCGGGCGCAGTGGCAGGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1291510129 Functional Loss SNV dbSNP153 33..33 33 - - - 21201 RMVar_ID_21201 Human_SNP_ID_149119651 A-to-I Human chr3 - 113715821 113715821 113715821 GCAATCTCGGCTCACTGCAATCTCCGCCACCTAGATTCAAGCAATTCTGTCTCGGCCTCCTGAGT GCAATCTCGGCTCACTGCAATCTCCGCCACCTGGATTCAAGCAATTCTGTCTCGGCCTCCTGAGT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs906240995 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14568070,Human_RBP_ID_18793965 21202 RMVar_ID_21202 Human_SNP_ID_149119663 A-to-I Human chr3 - 113715850 113715850 113715850 TTCTATCACCCAGGATGGAGCACAGTGGCGCAATCTCGGCTCACTGCAATCTCCGCCACCTAGAT TTCTATCACCCAGGATGGAGCACAGTGGCGCAGTCTCGGCTCACTGCAATCTCCGCCACCTAGAT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs369777595 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14568071 21203 RMVar_ID_21203 Human_SNP_ID_149122377 A-to-I Human chr3 - 113726897 113726897 113726897 TCAGCTACTCGTTAGGCTGAGGTGGGAAGATCACTTGAGCCTGAGAAGCGGAGGCTGCTGTGACC TCAGCTACTCGTTAGGCTGAGGTGGGAAGATCGCTTGAGCCTGAGAAGCGGAGGCTGCTGTGACC T C NAA50 Ensembl:ENSG00000121579 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs547516266 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14568590 21204 RMVar_ID_21204 Human_SNP_ID_149122378 A-to-I Human chr3 - 113726897 113726897 113726897 TCAGCTACTCGTTAGGCTGAGGTGGGAAGATCACTTGAGCCTGAGAAGCGGAGGCTGCTGTGACC TCAGCTACTCGTTAGGCTGAGGTGGGAAGATCCCTTGAGCCTGAGAAGCGGAGGCTGCTGTGACC T G NAA50 Ensembl:ENSG00000121579 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs547516266 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14568590 21205 RMVar_ID_21205 Human_SNP_ID_149122392 A-to-I Human chr3 - 113726960 113726960 113726960 TGGTGAAACCCTGTCTCTACAAAAAATTCAAAAATCAGCTGGGCGTGGTGGCATGTGCCTTCCTC TGGTGAAACCCTGTCTCTACAAAAAATTCAAAGATCAGCTGGGCGTGGTGGCATGTGCCTTCCTC T C NAA50 Ensembl:ENSG00000121579 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1371447107 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14568597,Human_RBP_ID_17991338,Human_RBP_ID_23016816,Human_RBP_ID_25765638 21206 RMVar_ID_21206 Human_SNP_ID_149123141 A-to-I Human chr3 - 113729671 113729671 113729671 GAAAGTGGTGGCATGCATTTGAGGTCTCAGCTACTTGGAAGGCTGAGGCAGGAGGATCCCCTGAG GAAAGTGGTGGCATGCATTTGAGGTCTCAGCTGCTTGGAAGGCTGAGGCAGGAGGATCCCCTGAG T C NAA50 Ensembl:ENSG00000121579 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1162716694 Functional Loss SNV dbSNP153 33..33 33 - - - 21207 RMVar_ID_21207 Human_SNP_ID_149133537 A-to-I Human chr3 + 113770528 113770528 113770528 GGCGAAATCCCGTCTCTACTAAAAATGCAAAAAATTAGCCAGGCATGGTGGCTCGTGCCTATAGT GGCGAAATCCCGTCTCTACTAAAAATGCAAAATATTAGCCAGGCATGGTGGCTCGTGCCTATAGT A T ATP6V1A Ensembl:ENSG00000114573 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1382687938 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_220341,RMVar_hsa_circ_105886 21208 RMVar_ID_21208 Human_SNP_ID_149134510 A-to-I Human chr3 + 113774151 113774151 113774151 CATCCCAGATTGTGAACAAGAAACAGGATGCTATAGCAGTCTACCGTAAACAGGGAAATTTCTTG CATCCCAGATTGTGAACAAGAAACAGGATGCTGTAGCAGTCTACCGTAAACAGGGAAATTTCTTG A G ATP6V1A Ensembl:ENSG00000114573 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1288777361 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_220341,RMVar_hsa_circ_105886 21209 RMVar_ID_21209 Human_SNP_ID_149134789 A-to-I Human chr3 + 113775304 113775304 113775304 CCTGCTGGAATGCAGTGGTGCAGTCTTGGCTCACTGCAACCTCCTCCTCCCGGGTTCAAGCAATT CCTGCTGGAATGCAGTGGTGCAGTCTTGGCTCTCTGCAACCTCCTCCTCCCGGGTTCAAGCAATT A T ATP6V1A Ensembl:ENSG00000114573 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1395824691 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_220341,RMVar_hsa_circ_105886 21210 RMVar_ID_21210 Human_SNP_ID_149134822 A-to-I Human chr3 + 113775419 113775418 113775419 ACCCAGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTTGCCGTGTTGGCTAGGCAAGTCTCGA ACCCAGCTAATTTTTGTATTTTTAGTAGAGAC_GGGTTTTGCCGTGTTGGCTAGGCAAGTCTCGA CA C ATP6V1A Ensembl:ENSG00000114573 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1426628477 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_14569950 RMVar_hsa_circ_220341,RMVar_hsa_circ_105886 21211 RMVar_ID_21211 Human_SNP_ID_149134823 A-to-I Human chr3 + 113775419 113775419 113775419 ACCCAGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTTGCCGTGTTGGCTAGGCAAGTCTCGA ACCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTTGCCGTGTTGGCTAGGCAAGTCTCGA A G ATP6V1A Ensembl:ENSG00000114573 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs967124999 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14569950 RMVar_hsa_circ_220341,RMVar_hsa_circ_105886 21212 RMVar_ID_21212 Human_SNP_ID_149195166 A-to-I Human chr3 - 114037776 114037776 114037776 ATTAACATAGCATTTACATTGTATTGGGTATCATAAGTAATCTAGAGATGATCTAGAGTATAAGG ATTAACATAGCATTTACATTGTATTGGGTATCGTAAGTAATCTAGAGATGATCTAGAGTATAAGG T C CCDC191 Ensembl:ENSG00000163617 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355353499 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10437,RMVar_hsa_circ_74864,RMVar_hsa_circ_36583,RMVar_hsa_circ_65698,RMVar_hsa_circ_315359,RMVar_hsa_circ_220370,RMVar_hsa_circ_360946,RMVar_hsa_circ_268656 21213 RMVar_ID_21213 Human_SNP_ID_149195171 A-to-I Human chr3 - 114037800 114037799 114037801 CCCCAAACAATACATATAACAAGTATTAACATAGCATTTACATTGTATTGGGTATCATAAGTAAT CCCCAAACAATACATATAACAAGTATTAACA__GCATTTACATTGTATTGGGTATCATAAGTAAT CTA C CCDC191 Ensembl:ENSG00000163617 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1166339325 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_10437,RMVar_hsa_circ_74864,RMVar_hsa_circ_36583,RMVar_hsa_circ_65698,RMVar_hsa_circ_315359,RMVar_hsa_circ_220370,RMVar_hsa_circ_360946,RMVar_hsa_circ_268656 21214 RMVar_ID_21214 Human_SNP_ID_149200535 A-to-I Human chr3 + 114061787 114061787 114061787 TTTTGTAGAGACAGGGTTTCATTGTGTTGCCCAGGCTGCTCTTGAACTCCTGGGCTCAAGCGATC TTTTGTAGAGACAGGGTTTCATTGTGTTGCCCCGGCTGCTCTTGAACTCCTGGGCTCAAGCGATC A C QTRT2 Ensembl:ENSG00000151576 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs967979399 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10062,RMVar_hsa_circ_40098 21215 RMVar_ID_21215 Human_SNP_ID_149200654 A-to-I Human chr3 + 114062262 114062262 114062262 CAGTGGTTGGGCACCTGTGGTCTCAGCTACTTAGGAGGCTGAGGTGGGAAGGTTACTTGAGCCTG CAGTGGTTGGGCACCTGTGGTCTCAGCTACTTGGGAGGCTGAGGTGGGAAGGTTACTTGAGCCTG A G QTRT2 Ensembl:ENSG00000151576 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1450571105 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10062,RMVar_hsa_circ_40098 21216 RMVar_ID_21216 Human_SNP_ID_149204747 A-to-I Human chr3 + 114079520 114079519 114079521 AGTTTGCGCCATTGCACTCCAGCCTGGGCAACAAGAGTAAGACTCCCTCTCAAAAAAAAAAAAGA AGTTTGCGCCATTGCACTCCAGCCTGGGCAAC__GAGTAAGACTCCCTCTCAAAAAAAAAAAAGA CAA C QTRT2 Ensembl:ENSG00000151576 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1193353922 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_304415,RMVar_hsa_circ_47864,RMVar_hsa_circ_220372,RMVar_hsa_circ_372338,RMVar_hsa_circ_303474,RMVar_hsa_circ_220374,RMVar_hsa_circ_60741 21217 RMVar_ID_21217 Human_SNP_ID_149267858 A-to-I Human chr3 - 114346826 114346826 114346826 TAAAAATTAACCAGGCATGGTGCTGCATGCCTATAGTTCCAGCTACTTGGGACGCTGAAATGGGA TAAAAATTAACCAGGCATGGTGCTGCATGCCTGTAGTTCCAGCTACTTGGGACGCTGAAATGGGA T C ZBTB20 Ensembl:ENSG00000181722 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1266520925 Functional Loss SNV dbSNP153 33..33 33 - - - 21218 RMVar_ID_21218 Human_SNP_ID_149277312 A-to-I Human chr3 - 114389107 114389107 114389107 TAACAACCTTATTTTTGTTTTTTGTCTGATCTAGATGCAGCCGCTCTCTGCTCCCTGCCCCAATG TAACAACCTTATTTTTGTTTTTTGTCTGATCTCGATGCAGCCGCTCTCTGCTCCCTGCCCCAATG T G ZBTB20 Ensembl:ENSG00000181722 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1278646502 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86426,RMVar_hsa_circ_15083,RMVar_hsa_circ_100592,RMVar_hsa_circ_101902,RMVar_hsa_circ_29125,RMVar_hsa_circ_61212,RMVar_hsa_circ_220383,RMVar_hsa_circ_220384,RMVar_hsa_circ_357309,RMVar_hsa_circ_364096,RMVar_hsa_circ_106940,RMVar_hsa_circ_110820,RMVar_hsa_circ_99266,RMVar_hsa_circ_220387,RMVar_hsa_circ_220388,RMVar_hsa_circ_220389,RMVar_hsa_circ_220386 21219 RMVar_ID_21219 Human_SNP_ID_149402160 A-to-I Human chr3 - 114937573 114937573 114937573 AATAAAAATACAAAAAATTAACAGGATGTGGTAGGATGCGCCTGTAGTCCCAGCTACTTGGGAAG AATAAAAATACAAAAAATTAACAGGATGTGGTGGGATGCGCCTGTAGTCCCAGCTACTTGGGAAG T C ZBTB20 Ensembl:ENSG00000181722 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1446467377 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 21220 RMVar_ID_21220 Human_SNP_ID_149408188 A-to-I Human chr3 - 114965544 114965543 114965544 GGATTTTTAAGTGAAATAAGCCAGGTACAGAAAGACAAATGCTGCATGATCTCACTTATATGTGG GGATTTTTAAGTGAAATAAGCCAGGTACAGAA_GACAAATGCTGCATGATCTCACTTATATGTGG CT C ZBTB20 Ensembl:ENSG00000181722 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1560444532 Functional Loss DEL 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 21221 RMVar_ID_21221 Human_SNP_ID_149617178 A-to-I Human chr3 - 115869673 115869673 115869673 CTCTTGAAAATGATTATAACAGAAAGAGAATGAGAGATTTAAAAGAAATTAATATTTAGTGAGTA CTCTTGAAAATGATTATAACAGAAAGAGAATGGGAGATTTAAAAGAAATTAATATTTAGTGAGTA T C LSAMP Ensembl:ENSG00000185565 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1020191044 Functional Loss SNV dbSNP153 33..33 33 - - - 21222 RMVar_ID_21222 Human_SNP_ID_149711847 A-to-I Human chr3 - 116264806 116264806 116264806 ACTCAGTTTTTTGAGACCAGCCTGAGCAACATAGCAAGATCTCTTCTCTGCAAAAAGTAAAAATT ACTCAGTTTTTTGAGACCAGCCTGAGCAACATTGCAAGATCTCTTCTCTGCAAAAAGTAAAAATT T A LSAMP Ensembl:ENSG00000185565 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1417697869 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104542,RMVar_hsa_circ_273991,RMVar_hsa_circ_220415,RMVar_hsa_circ_283585 21223 RMVar_ID_21223 Human_SNP_ID_149711848 A-to-I Human chr3 - 116264806 116264806 116264806 ACTCAGTTTTTTGAGACCAGCCTGAGCAACATAGCAAGATCTCTTCTCTGCAAAAAGTAAAAATT ACTCAGTTTTTTGAGACCAGCCTGAGCAACATGGCAAGATCTCTTCTCTGCAAAAAGTAAAAATT T C LSAMP Ensembl:ENSG00000185565 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1417697869 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104542,RMVar_hsa_circ_273991,RMVar_hsa_circ_220415,RMVar_hsa_circ_283585 21224 RMVar_ID_21224 Human_SNP_ID_149713698 A-to-I Human chr3 - 116271328 116271328 116271328 GGGATAGTGTGCCAAGTTGTAGTTAGTCTACAAGAGAAGCTGGACTTTCATTACTGTTCTGTGGG GGGATAGTGTGCCAAGTTGTAGTTAGTCTACAGGAGAAGCTGGACTTTCATTACTGTTCTGTGGG T C LSAMP Ensembl:ENSG00000185565 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs572862813 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104542,RMVar_hsa_circ_273991,RMVar_hsa_circ_220415,RMVar_hsa_circ_283585 21225 RMVar_ID_21225 Human_SNP_ID_149713711 A-to-I Human chr3 - 116271383 116271383 116271383 ACACCACAGAAATATAATCTACTTTGTGGACAAAGCATAAAATACAATTTGCTGAGGGATAGTGT ACACCACAGAAATATAATCTACTTTGTGGACAGAGCATAAAATACAATTTGCTGAGGGATAGTGT T C LSAMP Ensembl:ENSG00000185565 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1021287010 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104542,RMVar_hsa_circ_273991,RMVar_hsa_circ_220415,RMVar_hsa_circ_283585 21226 RMVar_ID_21226 Human_SNP_ID_149713712 A-to-I Human chr3 - 116271383 116271383 116271383 ACACCACAGAAATATAATCTACTTTGTGGACAAAGCATAAAATACAATTTGCTGAGGGATAGTGT ACACCACAGAAATATAATCTACTTTGTGGACACAGCATAAAATACAATTTGCTGAGGGATAGTGT T G LSAMP Ensembl:ENSG00000185565 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1021287010 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104542,RMVar_hsa_circ_273991,RMVar_hsa_circ_220415,RMVar_hsa_circ_283585 21227 RMVar_ID_21227 Human_SNP_ID_149713818 A-to-I Human chr3 - 116271756 116271756 116271756 AATGAAAGTGCAGCTTCTCTTTTAGACTAACTACAAATTGGCACACTATCCGTCAGCACGTTGCA AATGAAAGTGCAGCTTCTCTTTTAGACTAACTGCAAATTGGCACACTATCCGTCAGCACGTTGCA T C LSAMP Ensembl:ENSG00000185565 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1223422072 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104542,RMVar_hsa_circ_273991,RMVar_hsa_circ_220415,RMVar_hsa_circ_283585 21228 RMVar_ID_21228 Human_SNP_ID_149728968 A-to-I Human chr3 - 116333451 116333451 116333451 TTGCTCACTGCAACCTCCGCCTCCTGGGTTCAATTCTCTGCCTCAGCATCCTGAGTAGCTGGGAT TTGCTCACTGCAACCTCCGCCTCCTGGGTTCATTTCTCTGCCTCAGCATCCTGAGTAGCTGGGAT T A LSAMP Ensembl:ENSG00000185565 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs534075506 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104542,RMVar_hsa_circ_273991,RMVar_hsa_circ_220415,RMVar_hsa_circ_283585 21229 RMVar_ID_21229 Human_SNP_ID_149728969 A-to-I Human chr3 - 116333451 116333451 116333451 TTGCTCACTGCAACCTCCGCCTCCTGGGTTCAATTCTCTGCCTCAGCATCCTGAGTAGCTGGGAT TTGCTCACTGCAACCTCCGCCTCCTGGGTTCAGTTCTCTGCCTCAGCATCCTGAGTAGCTGGGAT T C LSAMP Ensembl:ENSG00000185565 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs534075506 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104542,RMVar_hsa_circ_273991,RMVar_hsa_circ_220415,RMVar_hsa_circ_283585 21230 RMVar_ID_21230 Human_SNP_ID_150074772 A-to-I Human chr3 - 117689541 117689541 117689541 TGTTTTGTTTTGTTTTTGTTTTTGAAGACGGAATCTTGCTCTGTTGCCAGGCTGGAGTGCACTGG TGTTTTGTTTTGTTTTTGTTTTTGAAGACGGACTCTTGCTCTGTTGCCAGGCTGGAGTGCACTGG T G LINC02024,AC092691.1 Ensembl:ENSG00000241213,Ensembl:ENSG00000239268 lincRNA,lincRNA intron,intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs957847490 Functional Loss SNV dbSNP153 33..33 33 - - - 21231 RMVar_ID_21231 Human_SNP_ID_150471681 A-to-I Human chr3 + 119309715 119309715 119309715 CCAGGAGGTCAAAGCCGCAGTGAGCTGTGATCATGCCACTGCATTCCAGCCTGAGACAGAGTGAG CCAGGAGGTCAAAGCCGCAGTGAGCTGTGATCCTGCCACTGCATTCCAGCCTGAGACAGAGTGAG A C ARHGAP31 Ensembl:ENSG00000031081 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924314961 Functional Loss SNV dbSNP153 33..33 33 - - - 21232 RMVar_ID_21232 Human_SNP_ID_150484332 A-to-I Human chr3 + 119362641 119362641 119362641 AATACAAAAATTAGCTGGGCATGGTGGCAGGCACCTGTAATCCCTTCTACTCGGGAGGCTGAGGC AATACAAAAATTAGCTGGGCATGGTGGCAGGCTCCTGTAATCCCTTCTACTCGGGAGGCTGAGGC A T ARHGAP31 Ensembl:ENSG00000031081 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1467937046 Functional Loss SNV dbSNP153 33..33 33 - - - 21233 RMVar_ID_21233 Human_SNP_ID_150503666 A-to-I Human chr3 - 119445074 119445073 119445074 GTCCAGAGACGGTTGCTTTTTTTTTTTGAGACAGGGTTTTGCTCTGTCATCCAGGCGGGAGTGCA GTCCAGAGACGGTTGCTTTTTTTTTTTGAGAC_GGGTTTTGCTCTGTCATCCAGGCGGGAGTGCA CT C TMEM39A Ensembl:ENSG00000176142 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985463244 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_2742222,Human_RBP_ID_14577399 RMVar_hsa_circ_12984,RMVar_hsa_circ_18007,RMVar_hsa_circ_220457,RMVar_hsa_circ_94883,RMVar_hsa_circ_350462,RMVar_hsa_circ_369403,RMVar_hsa_circ_341357,RMVar_hsa_circ_220458,RMVar_hsa_circ_9425,RMVar_hsa_circ_220456 21234 RMVar_ID_21234 Human_SNP_ID_150503667 A-to-I Human chr3 - 119445074 119445074 119445074 GTCCAGAGACGGTTGCTTTTTTTTTTTGAGACAGGGTTTTGCTCTGTCATCCAGGCGGGAGTGCA GTCCAGAGACGGTTGCTTTTTTTTTTTGAGACGGGGTTTTGCTCTGTCATCCAGGCGGGAGTGCA T C TMEM39A Ensembl:ENSG00000176142 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs908089281 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2742222,Human_RBP_ID_14577399 RMVar_hsa_circ_12984,RMVar_hsa_circ_18007,RMVar_hsa_circ_220457,RMVar_hsa_circ_94883,RMVar_hsa_circ_350462,RMVar_hsa_circ_369403,RMVar_hsa_circ_341357,RMVar_hsa_circ_220458,RMVar_hsa_circ_9425,RMVar_hsa_circ_220456 21235 RMVar_ID_21235 Human_SNP_ID_150504307 A-to-I Human chr3 - 119447749 119447749 119447749 CGTGGTGGTGTACGCCTGTATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAACCGCTTGAACCCA CGTGGTGGTGTACGCCTGTATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAACCGCTTGAACCCA T C TMEM39A Ensembl:ENSG00000176142 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1309334283 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12984,RMVar_hsa_circ_18007,RMVar_hsa_circ_220457,RMVar_hsa_circ_94883,RMVar_hsa_circ_350462,RMVar_hsa_circ_369403,RMVar_hsa_circ_341357,RMVar_hsa_circ_220458,RMVar_hsa_circ_9425,RMVar_hsa_circ_220456,RMVar_hsa_circ_220462,RMVar_hsa_circ_296375,RMVar_hsa_circ_337285,RMVar_hsa_circ_50312,RMVar_hsa_circ_220461 21236 RMVar_ID_21236 Human_SNP_ID_150504308 A-to-I Human chr3 - 119447753 119447753 119447753 TGGGCGTGGTGGTGTACGCCTGTATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAACCGCTTGAA TGGGCGTGGTGGTGTACGCCTGTATCCCAGCTGCTCAGGAGGCTGAGGCAGGAGAACCGCTTGAA T C TMEM39A Ensembl:ENSG00000176142 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1171332325 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12984,RMVar_hsa_circ_18007,RMVar_hsa_circ_220457,RMVar_hsa_circ_94883,RMVar_hsa_circ_350462,RMVar_hsa_circ_369403,RMVar_hsa_circ_341357,RMVar_hsa_circ_220458,RMVar_hsa_circ_9425,RMVar_hsa_circ_220456,RMVar_hsa_circ_220462,RMVar_hsa_circ_296375,RMVar_hsa_circ_337285,RMVar_hsa_circ_50312,RMVar_hsa_circ_220461 21237 RMVar_ID_21237 Human_SNP_ID_150510562 A-to-I Human chr3 + 119473060 119473059 119473060 CCTGTCTCAAATAAATAATAATAAAGAACAATAAAAAAGAAAGATTATTTAATATCTCACTACCC CCTGTCTCAAATAAATAATAATAAAGAACAAT_AAAAAGAAAGATTATTTAATATCTCACTACCC TA T POGLUT1 Ensembl:ENSG00000163389 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1560030562 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_4516,RMVar_hsa_circ_335663,RMVar_hsa_circ_342486,RMVar_hsa_circ_329329,RMVar_hsa_circ_50305,RMVar_hsa_circ_59725,RMVar_hsa_circ_49987,RMVar_hsa_circ_220467 21238 RMVar_ID_21238 Human_SNP_ID_150517259 A-to-I Human chr3 + 119500853 119500853 119500853 GAGCCAGGCAGAAATTTATCATAACCGGTTTGATGCTGTGGTATGTACTGGTGATCTAAAGAAAT GAGCCAGGCAGAAATTTATCATAACCGGTTTGCTGCTGTGGTATGTACTGGTGATCTAAAGAAAT A C TIMMDC1 Ensembl:ENSG00000113845 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1390999770 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23962661 Human_Splice_Rec_470889,Human_Splice_Rec_470901,Human_Splice_Rec_470931,Human_Splice_Rec_470939 RMVar_hsa_circ_220470,RMVar_hsa_circ_85574,RMVar_hsa_circ_220474,RMVar_hsa_circ_95868,RMVar_hsa_circ_273828,RMVar_hsa_circ_277773,RMVar_hsa_circ_370391,RMVar_hsa_circ_273012,RMVar_hsa_circ_220475,RMVar_hsa_circ_220472,RMVar_hsa_circ_220473,RMVar_hsa_circ_220471 21239 RMVar_ID_21239 Human_SNP_ID_150518661 A-to-I Human chr3 + 119506276 119506276 119506276 GCCAGGCACAGTGGCTCACGCCTGTAACCAGCACTTTGGGAGGCCAAGGTGGGCAGATCGCTTGA GCCAGGCACAGTGGCTCACGCCTGTAACCAGCTCTTTGGGAGGCCAAGGTGGGCAGATCGCTTGA A T TIMMDC1 Ensembl:ENSG00000113845 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886897900 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95370,RMVar_hsa_circ_220474,RMVar_hsa_circ_277773,RMVar_hsa_circ_273012,RMVar_hsa_circ_220475,RMVar_hsa_circ_278890,RMVar_hsa_circ_274942,RMVar_hsa_circ_220476,RMVar_hsa_circ_220478,RMVar_hsa_circ_220477,RMVar_hsa_circ_220481,RMVar_hsa_circ_314048 21240 RMVar_ID_21240 Human_SNP_ID_150519470 A-to-I Human chr3 + 119509860 119509860 119509860 GGCATATGCCACCATACCCGGCTAATTTTTGTATTTTTAGCAGAGACAGGGTTTCACCATGTTAG GGCATATGCCACCATACCCGGCTAATTTTTGTGTTTTTAGCAGAGACAGGGTTTCACCATGTTAG A G TIMMDC1 Ensembl:ENSG00000113845 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1266923439 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95370,RMVar_hsa_circ_220474,RMVar_hsa_circ_277773,RMVar_hsa_circ_273012,RMVar_hsa_circ_220475,RMVar_hsa_circ_278890,RMVar_hsa_circ_274942,RMVar_hsa_circ_220476,RMVar_hsa_circ_220478,RMVar_hsa_circ_220477,RMVar_hsa_circ_220481,RMVar_hsa_circ_314048 21241 RMVar_ID_21241 Human_SNP_ID_150519475 A-to-I Human chr3 + 119509883 119509883 119509883 AATTTTTGTATTTTTAGCAGAGACAGGGTTTCACCATGTTAGCCAGGATGGTCTCAATCTCCTGA AATTTTTGTATTTTTAGCAGAGACAGGGTTTCGCCATGTTAGCCAGGATGGTCTCAATCTCCTGA A G TIMMDC1 Ensembl:ENSG00000113845 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1473604011 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95370,RMVar_hsa_circ_220474,RMVar_hsa_circ_277773,RMVar_hsa_circ_273012,RMVar_hsa_circ_220475,RMVar_hsa_circ_278890,RMVar_hsa_circ_274942,RMVar_hsa_circ_220476,RMVar_hsa_circ_220478,RMVar_hsa_circ_220477,RMVar_hsa_circ_220481,RMVar_hsa_circ_314048 21242 RMVar_ID_21242 Human_SNP_ID_150520138 A-to-I Human chr3 + 119512926 119512926 119512926 CAATACCCAGCTAATTTTTGTATCTTTAGTAGAGGCAGGGTTTTGCCATGTTGTCCAGGCTGACT CAATACCCAGCTAATTTTTGTATCTTTAGTAGTGGCAGGGTTTTGCCATGTTGTCCAGGCTGACT A T TIMMDC1 Ensembl:ENSG00000113845 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1029077870 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14578214 RMVar_hsa_circ_95370,RMVar_hsa_circ_220474,RMVar_hsa_circ_277773,RMVar_hsa_circ_273012,RMVar_hsa_circ_220475,RMVar_hsa_circ_278890,RMVar_hsa_circ_274942,RMVar_hsa_circ_220476,RMVar_hsa_circ_220478,RMVar_hsa_circ_220477,RMVar_hsa_circ_220481,RMVar_hsa_circ_314048 21243 RMVar_ID_21243 Human_SNP_ID_150523624 A-to-I Human chr3 - 119527980 119527980 119527980 ATGTCCCCTTGGCAAAGAGGTAAAGAGGGAGCATTGTAAATCACCCCTGGTATAAGAACAACTGC ATGTCCCCTTGGCAAAGAGGTAAAGAGGGAGCGTTGTAAATCACCCCTGGTATAAGAACAACTGC T C CD80 Ensembl:ENSG00000121594 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6778945 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_1974,GWAS_ID_1975,GWAS_ID_1976,GWAS_ID_1977,GWAS_ID_1978 21244 RMVar_ID_21244 Human_SNP_ID_150523783 A-to-I Human chr3 - 119528702 119528702 119528702 GGCCAGGATGGTCTTGATCTCCTGACCTCGTGATCCGCCTGCCTTGGCTTCCCAAAGTGCTGGGA GGCCAGGATGGTCTTGATCTCCTGACCTCGTGTTCCGCCTGCCTTGGCTTCCCAAAGTGCTGGGA T A CD80 Ensembl:ENSG00000121594 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs565012263 Functional Loss SNV dbSNP153 33..33 33 - - - 21245 RMVar_ID_21245 Human_SNP_ID_150523800 A-to-I Human chr3 - 119528756 119528756 119528756 ACGCCTGACTAATTTTTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGATGG ACGCCTGACTAATTTTTTTTTGTATTTTTAGTGGAGACGGGGTTTCACCATGTTGGCCAGGATGG T C CD80 Ensembl:ENSG00000121594 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs778872949 Functional Loss SNV dbSNP153 33..33 33 - - - 21246 RMVar_ID_21246 Human_SNP_ID_150523989 A-to-I Human chr3 - 119529633 119529633 119529633 TTTCCGGACACCTCCTACGTGTGTGGCACTCTACTAGGCACTGGAATTACAATGACAAGAAGTCA TTTCCGGACACCTCCTACGTGTGTGGCACTCTGCTAGGCACTGGAATTACAATGACAAGAAGTCA T C CD80 Ensembl:ENSG00000121594 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs9837692 Functional Loss SNV dbSNP153 33..33 33 - - - 21247 RMVar_ID_21247 Human_SNP_ID_150524311 A-to-I Human chr3 - 119531024 119531024 119531024 AGAACTAAGCATCACACATTGAGAATCTCTTCATAATCTAGGCACAGATAATCTTTAACACTAAA AGAACTAAGCATCACACATTGAGAATCTCTTCGTAATCTAGGCACAGATAATCTTTAACACTAAA T C CD80 Ensembl:ENSG00000121594 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1797839 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_1979 21248 RMVar_ID_21248 Human_SNP_ID_150525446 A-to-I Human chr3 - 119536205 119536205 119536205 GCCCTGTTGCCCAGGCTGGAGTGCAGTGGCACAATCTCAGCTCACTGCAACCTCCACCTTCCAGG GCCCTGTTGCCCAGGCTGGAGTGCAGTGGCACCATCTCAGCTCACTGCAACCTCCACCTTCCAGG T G CD80 Ensembl:ENSG00000121594 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1406759416 Functional Loss SNV dbSNP153 33..33 33 - - - 21249 RMVar_ID_21249 Human_SNP_ID_150526477 A-to-I Human chr3 - 119540866 119540866 119540866 TTTTTTATTTTTAGTAGAGACAAGGTTTCACTATGTTGTCCAGGGTGGTCTCAAACTCCTGACCT TTTTTTATTTTTAGTAGAGACAAGGTTTCACTTTGTTGTCCAGGGTGGTCTCAAACTCCTGACCT T A CD80 Ensembl:ENSG00000121594 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs983987008 Functional Loss SNV dbSNP153 33..33 33 - - - 21250 RMVar_ID_21250 Human_SNP_ID_150526478 A-to-I Human chr3 - 119540866 119540866 119540866 TTTTTTATTTTTAGTAGAGACAAGGTTTCACTATGTTGTCCAGGGTGGTCTCAAACTCCTGACCT TTTTTTATTTTTAGTAGAGACAAGGTTTCACTGTGTTGTCCAGGGTGGTCTCAAACTCCTGACCT T C CD80 Ensembl:ENSG00000121594 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs983987008 Functional Loss SNV dbSNP153 33..33 33 - - - 21251 RMVar_ID_21251 Human_SNP_ID_150619561 A-to-I Human chr3 - 119921974 119921974 119921974 CGCGACCATGCCCAGCTAATTTTTGTGTTTTTAGTGGAGATGTGGTTTCATCATGTTGGCTGGGC CGCGACCATGCCCAGCTAATTTTTGTGTTTTTGGTGGAGATGTGGTTTCATCATGTTGGCTGGGC T C GSK3B Ensembl:ENSG00000082701 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1324236255 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14579187,Human_RBP_ID_25689681 RMVar_hsa_circ_220492,RMVar_hsa_circ_42438,RMVar_hsa_circ_340761,RMVar_hsa_circ_62483,RMVar_hsa_circ_334139,RMVar_hsa_circ_338412,RMVar_hsa_circ_354613,RMVar_hsa_circ_220504,RMVar_hsa_circ_220503,RMVar_hsa_circ_99255,RMVar_hsa_circ_220508,RMVar_hsa_circ_293082,RMVar_hsa_circ_347331,RMVar_hsa_circ_301026,RMVar_hsa_circ_300390,RMVar_hsa_circ_220509,RMVar_hsa_circ_377669,RMVar_hsa_circ_287967,RMVar_hsa_circ_298490,RMVar_hsa_circ_220515,RMVar_hsa_circ_220516,RMVar_hsa_circ_220517,RMVar_hsa_circ_220514,RMVar_hsa_circ_118478,RMVar_hsa_circ_342267,RMVar_hsa_circ_220518,RMVar_hsa_circ_351028 21252 RMVar_ID_21252 Human_SNP_ID_150628814 A-to-I Human chr3 - 119958501 119958501 119958501 GCTAATTTATTTTTATTTTTTGTAGAGATGCAATCTCCCTGTGTTGTCAGGCTGGTCTTGAACTC GCTAATTTATTTTTATTTTTTGTAGAGATGCAGTCTCCCTGTGTTGTCAGGCTGGTCTTGAACTC T C GSK3B Ensembl:ENSG00000082701 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs527785220 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 21253 RMVar_ID_21253 Human_SNP_ID_150628815 A-to-I Human chr3 - 119958501 119958501 119958501 GCTAATTTATTTTTATTTTTTGTAGAGATGCAATCTCCCTGTGTTGTCAGGCTGGTCTTGAACTC GCTAATTTATTTTTATTTTTTGTAGAGATGCACTCTCCCTGTGTTGTCAGGCTGGTCTTGAACTC T G GSK3B Ensembl:ENSG00000082701 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs527785220 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 21254 RMVar_ID_21254 Human_SNP_ID_58205550 A-to-I Human chr2 - 1634061 1634061 1634061 TCATGACAACGTCCAGCTGGTGCTGTTACAGAAGGCAGTGCAGGAGGCTTCCAACCAGAGCATCT TCATGACAACGTCCAGCTGGTGCTGTTACAGACGGCAGTGCAGGAGGCTTCCAACCAGAGCATCT T G PXDN Ensembl:ENSG00000130508 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1315792297 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5588732,Human_RBP_ID_17273959,Human_RBP_ID_27283709 Human_miRNA_ID_3003135 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_93659,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_196625,RMVar_hsa_circ_196623,RMVar_hsa_circ_196621,RMVar_hsa_circ_196618,RMVar_hsa_circ_196619,RMVar_hsa_circ_196617,RMVar_hsa_circ_196615 21255 RMVar_ID_21255 Human_SNP_ID_58667718 A-to-I Human chr2 - 3345477 3345477 3345477 GGGATCACAGGCGTGCACCACCATGCCCGGCTAATTTTTATATTTTTAGTAGAGACGGGGTTTCA GGGATCACAGGCGTGCACCACCATGCCCGGCTGATTTTTATATTTTTAGTAGAGACGGGGTTTCA T C EIPR1 Ensembl:ENSG00000032389 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1224600027 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_299378,RMVar_hsa_circ_196692,RMVar_hsa_circ_196691 21256 RMVar_ID_21256 Human_SNP_ID_58695179 A-to-I Human chr2 + 3445310 3445310 3445310 GGGAGGCTGAGGCATGAGAATCGCTTGAACCCAGGAGGCTGAGGTTGCAGTAAGCCGAGATCAAG GGGAGGCTGAGGCATGAGAATCGCTTGAACCCCGGAGGCTGAGGTTGCAGTAAGCCGAGATCAAG A C TRAPPC12 Ensembl:ENSG00000171853 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1406444884 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13868134 RMVar_hsa_circ_6036,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_92909,RMVar_hsa_circ_103367,RMVar_hsa_circ_196702,RMVar_hsa_circ_122158,RMVar_hsa_circ_196705,RMVar_hsa_circ_196706,RMVar_hsa_circ_196707 21257 RMVar_ID_21257 Human_SNP_ID_58704222 A-to-I Human chr2 + 3477740 3477740 3477740 AAACAGCTGAAAAGTATTTTCAAGACGTTGAGAAAGTAACACAGAAATTAGATGGACTACAGGGT AAACAGCTGAAAAGTATTTTCAAGACGTTGAGGAAGTAACACAGAAATTAGATGGACTACAGGGT A G TRAPPC12 Ensembl:ENSG00000171853 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs764323391 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_60268,Human_RBP_ID_1916623,Human_RBP_ID_3624334,Human_RBP_ID_13868994,Human_RBP_ID_18759862 Human_Splice_Rec_212898,Human_Splice_Rec_212899,Human_Splice_Rec_212920,Human_Splice_Rec_212921,Human_Splice_Rec_213016,Human_Splice_Rec_213017,Human_Splice_Rec_213032,Human_Splice_Rec_213033,Human_Splice_Rec_213042,Human_Splice_Rec_213043,Human_Splice_Rec_213048,Human_Splice_Rec_213049,Human_Splice_Rec_213054,Human_Splice_Rec_213060,Human_Splice_Rec_213061,Human_Splice_Rec_213068,Human_Splice_Rec_213069,Human_Splice_Rec_213073 RMVar_hsa_circ_100740,RMVar_hsa_circ_196695,RMVar_hsa_circ_95742,RMVar_hsa_circ_196701,RMVar_hsa_circ_103367,RMVar_hsa_circ_122158,RMVar_hsa_circ_196705,RMVar_hsa_circ_196707,RMVar_hsa_circ_107998,RMVar_hsa_circ_196710,RMVar_hsa_circ_196711,RMVar_hsa_circ_122715,RMVar_hsa_circ_80507,RMVar_hsa_circ_196712,RMVar_hsa_circ_196713 21258 RMVar_ID_21258 Human_SNP_ID_58704827 A-to-I Human chr2 + 3479485 3479485 3479485 CTGGCCTAGCTGCCTCCAACACACTACGTCAGAAGGACCCGGGTCTTTGAAACTGTGTCTTGAAG CTGGCCTAGCTGCCTCCAACACACTACGTCAGGAGGACCCGGGTCTTTGAAACTGTGTCTTGAAG A G TRAPPC12 Ensembl:ENSG00000171853 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1360833375 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_549963,Human_RBP_ID_1916627,Human_RBP_ID_3624339 RMVar_hsa_circ_100740,RMVar_hsa_circ_196695,RMVar_hsa_circ_95742,RMVar_hsa_circ_196701,RMVar_hsa_circ_103367,RMVar_hsa_circ_122158,RMVar_hsa_circ_196705,RMVar_hsa_circ_196707,RMVar_hsa_circ_196711,RMVar_hsa_circ_113030,RMVar_hsa_circ_122715,RMVar_hsa_circ_80507,RMVar_hsa_circ_196712,RMVar_hsa_circ_196713,RMVar_hsa_circ_96186,RMVar_hsa_circ_196714,RMVar_hsa_circ_196715 21259 RMVar_ID_21259 Human_SNP_ID_58710520 A-to-I Human chr2 - 3498750 3498750 3498750 TGTAAAGAGTCACCTTCATTTTCTGTAACTCAATCAAGACTGGTGGGTCCATGGCCCTGTGTTAG TGTAAAGAGTCACCTTCATTTTCTGTAACTCAGTCAAGACTGGTGGGTCCATGGCCCTGTGTTAG T C ADI1 Ensembl:ENSG00000182551 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs911376031 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_776577,Human_RBP_ID_1916633,Human_RBP_ID_5502162,Human_RBP_ID_17276042,Human_RBP_ID_17391170,Human_RBP_ID_17658309,Human_RBP_ID_17956092,Human_RBP_ID_18316625,Human_RBP_ID_26818076,Human_RBP_ID_27289860,Human_RBP_ID_27479809 Human_miRNA_ID_1954184,Human_miRNA_ID_3061153 RMVar_hsa_circ_120814,RMVar_hsa_circ_196716 21260 RMVar_ID_21260 Human_SNP_ID_58723629 A-to-I Human chr2 - 3545012 3545012 3545012 CTAGCACTTTGGGAGGCCAAGGCGGGCAGATCACTTGAGGTCAGGAGTTTGAGACCAGCTTGGCC CTAGCACTTTGGGAGGCCAAGGCGGGCAGATCGCTTGAGGTCAGGAGTTTGAGACCAGCTTGGCC T C AC108488.2,RNASEH1 Ensembl:ENSG00000286905,Ensembl:ENSG00000171865 Protein coding,Protein coding intron,3'UTR GSE38233;GSE99789;GSE107867;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,EC109;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29796672,30559470,31158229,32596459 RNA-Seq:(High) rs1053580478 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25537424 21261 RMVar_ID_21261 Human_SNP_ID_58726150 A-to-I Human chr2 - 3553126 3553126 3553126 CTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGTGCCCGCCATCACGCCTGGCTAATTTTT CTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTGCAGGTGCCCGCCATCACGCCTGGCTAATTTTT T C AC108488.2,RNASEH1 Ensembl:ENSG00000286905,Ensembl:ENSG00000171865 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs891182130 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70 21262 RMVar_ID_21262 Human_SNP_ID_58726151 A-to-I Human chr2 - 3553126 3553126 3553126 CTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGTGCCCGCCATCACGCCTGGCTAATTTTT CTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTCCAGGTGCCCGCCATCACGCCTGGCTAATTTTT T G AC108488.2,RNASEH1 Ensembl:ENSG00000286905,Ensembl:ENSG00000171865 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs891182130 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70 21263 RMVar_ID_21263 Human_SNP_ID_58726294 A-to-I Human chr2 - 3553528 3553528 3553528 AAAATTAGCTGGGTGTGGTGGTGGGTGCCTGTAATCCCAGCTACTTGGGAGGCTGTGGCAGAGAA AAAATTAGCTGGGTGTGGTGGTGGGTGCCTGTGATCCCAGCTACTTGGGAGGCTGTGGCAGAGAA T C AC108488.2,RNASEH1 Ensembl:ENSG00000286905,Ensembl:ENSG00000171865 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1294963944 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70 21264 RMVar_ID_21264 Human_SNP_ID_58727085 A-to-I Human chr2 - 3556127 3556127 3556127 CTCTGTTGCGCAGGCTGGAGTGCAGTGGCACAATCTTGGCTCACTGCAGTCTCTGCCTCCTGCGT CTCTGTTGCGCAGGCTGGAGTGCAGTGGCACAGTCTTGGCTCACTGCAGTCTCTGCCTCCTGCGT T C AC108488.2,RNASEH1 Ensembl:ENSG00000286905,Ensembl:ENSG00000171865 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1298643113 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70 21265 RMVar_ID_21265 Human_SNP_ID_58727202 A-to-I Human chr2 - 3556470 3556470 3556470 TGAAACTCCATCTCTACTAAAATACAAAAATTAGCTGGGCATGGTGGCGCACACCTGTAATCCCA TGAAACTCCATCTCTACTAAAATACAAAAATTCGCTGGGCATGGTGGCGCACACCTGTAATCCCA T G AC108488.2,RNASEH1 Ensembl:ENSG00000286905,Ensembl:ENSG00000171865 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1414081099 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70 21266 RMVar_ID_21266 Human_SNP_ID_60083097 A-to-I Human chr2 - 8742320 8742320 8742320 GAGGCAGGAGGATGACTTGAGCCCACAAGTTCAAGACCAGCCTAGGCAACATAGCAAGACCATTT GAGGCAGGAGGATGACTTGAGCCCACAAGTTCGAGACCAGCCTAGGCAACATAGCAAGACCATTT T C KIDINS220 Ensembl:ENSG00000134313 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1244212102 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8497,RMVar_hsa_circ_24990,RMVar_hsa_circ_72934,RMVar_hsa_circ_316967,RMVar_hsa_circ_317641,RMVar_hsa_circ_55834,RMVar_hsa_circ_37729,RMVar_hsa_circ_196749,RMVar_hsa_circ_4280,RMVar_hsa_circ_9963,RMVar_hsa_circ_196750,RMVar_hsa_circ_196752,RMVar_hsa_circ_348151,RMVar_hsa_circ_267674 21267 RMVar_ID_21267 Human_SNP_ID_60084540 A-to-I Human chr2 - 8747457 8747452 8747457 ACATTTCAATCAAATGGCAGGAATTAAACAAGATAAGGGAAATTCTTCCAATGAACTATTGAATC ACATTTCAATCAAATGGCAGGAATTAAACAAG_____GGAAATTCTTCCAATGAACTATTGAATC CCTTAT C KIDINS220 Ensembl:ENSG00000134313 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1328377264 Functional Loss DEL dbSNP153 33..37 33 - - - RMVar_hsa_circ_8497,RMVar_hsa_circ_24990,RMVar_hsa_circ_72934,RMVar_hsa_circ_316967,RMVar_hsa_circ_317641,RMVar_hsa_circ_55834,RMVar_hsa_circ_37729,RMVar_hsa_circ_196749,RMVar_hsa_circ_4280,RMVar_hsa_circ_9963,RMVar_hsa_circ_196750,RMVar_hsa_circ_196752,RMVar_hsa_circ_348151,RMVar_hsa_circ_267674 21268 RMVar_ID_21268 Human_SNP_ID_60198236 A-to-I Human chr2 + 9210761 9210761 9210761 TATTTTTAGTAGAGATGGGGTTTCACCGTGTTAGCCAGGATGGTCGATGGTCTAGATCTCCTGAC TATTTTTAGTAGAGATGGGGTTTCACCGTGTTGGCCAGGATGGTCGATGGTCTAGATCTCCTGAC A G ASAP2 Ensembl:ENSG00000151693 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1261781059 Functional Loss SNV dbSNP153 33..33 33 - - - 21269 RMVar_ID_21269 Human_SNP_ID_60240341 A-to-I Human chr2 + 9381843 9381843 9381843 GAGAATGGACTTGAGCTTAGGAGTTCAAGACTACAGTGAGCCATGATTATGCCAATGCGCACCAG GAGAATGGACTTGAGCTTAGGAGTTCAAGACTGCAGTGAGCCATGATTATGCCAATGCGCACCAG A G ASAP2 Ensembl:ENSG00000151693 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1332843652 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4650,RMVar_hsa_circ_85556,RMVar_hsa_circ_196823,RMVar_hsa_circ_269584,RMVar_hsa_circ_339776,RMVar_hsa_circ_13668,RMVar_hsa_circ_337495,RMVar_hsa_circ_35204,RMVar_hsa_circ_196838,RMVar_hsa_circ_312225,RMVar_hsa_circ_5631,RMVar_hsa_circ_334594,RMVar_hsa_circ_196847 21270 RMVar_ID_21270 Human_SNP_ID_60248244 A-to-I Human chr2 - 9410117 9410117 9410117 ACTCGGGCTGGGCGCGGTGGCTCAGGCCTATAATTCCAGCACTTTGGGAGGCCGAGGTGGGTGAA ACTCGGGCTGGGCGCGGTGGCTCAGGCCTATAGTTCCAGCACTTTGGGAGGCCGAGGTGGGTGAA T C ITGB1BP1 Ensembl:ENSG00000119185 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs541695617 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26187,RMVar_hsa_circ_311960,RMVar_hsa_circ_196850,RMVar_hsa_circ_301507,RMVar_hsa_circ_196851 21271 RMVar_ID_21271 Human_SNP_ID_60248245 A-to-I Human chr2 - 9410120 9410120 9410120 AGAACTCGGGCTGGGCGCGGTGGCTCAGGCCTATAATTCCAGCACTTTGGGAGGCCGAGGTGGGT AGAACTCGGGCTGGGCGCGGTGGCTCAGGCCTGTAATTCCAGCACTTTGGGAGGCCGAGGTGGGT T C ITGB1BP1 Ensembl:ENSG00000119185 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1218903599 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13982740 RMVar_hsa_circ_26187,RMVar_hsa_circ_311960,RMVar_hsa_circ_196850,RMVar_hsa_circ_301507,RMVar_hsa_circ_196851 21272 RMVar_ID_21272 Human_SNP_ID_60248677 A-to-I Human chr2 - 9411860 9411860 9411860 TTTTGTATTTTCAGTAGAGACAGGGTTTTTCCATGTTGGTCAGGCTGGTCTTGAACTCCCGACCT TTTTGTATTTTCAGTAGAGACAGGGTTTTTCCGTGTTGGTCAGGCTGGTCTTGAACTCCCGACCT T C ITGB1BP1 Ensembl:ENSG00000119185 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1244472014 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26187,RMVar_hsa_circ_311960,RMVar_hsa_circ_196850,RMVar_hsa_circ_301507,RMVar_hsa_circ_196851 21273 RMVar_ID_21273 Human_SNP_ID_60256393 A-to-I Human chr2 + 9444325 9444325 9444325 AATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCGTCTTGGCCGGGCTGGTCTTGAACTCCTGA AATTTTTGTATTTTTAGTAGAGATGGGGTTTCGCCGTCTTGGCCGGGCTGGTCTTGAACTCCTGA A G CPSF3 Ensembl:ENSG00000119203 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1220283541 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_52,RMVar_hsa_circ_118941,RMVar_hsa_circ_196859,RMVar_hsa_circ_107887,RMVar_hsa_circ_196860,RMVar_hsa_circ_13109,RMVar_hsa_circ_77677,RMVar_hsa_circ_196867,RMVar_hsa_circ_196868,RMVar_hsa_circ_371619,RMVar_hsa_circ_373941,RMVar_hsa_circ_26490,RMVar_hsa_circ_43012,RMVar_hsa_circ_110741,RMVar_hsa_circ_196870,RMVar_hsa_circ_196871,RMVar_hsa_circ_377354,RMVar_hsa_circ_11181,RMVar_hsa_circ_25553,RMVar_hsa_circ_68155,RMVar_hsa_circ_196873,RMVar_hsa_circ_70594,RMVar_hsa_circ_196875,RMVar_hsa_circ_105068,RMVar_hsa_circ_116674,RMVar_hsa_circ_196876 21274 RMVar_ID_21274 Human_SNP_ID_60257853 A-to-I Human chr2 + 9450431 9450431 9450431 CGTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGACCCACCGTGCCCAGTCTGAGGCTCA CGTGCCTTGGCCTCCCAAAGTGCTGGGATTACCGGCGTGACCCACCGTGCCCAGTCTGAGGCTCA A C CPSF3 Ensembl:ENSG00000119203 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1385237176 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118941,RMVar_hsa_circ_196859,RMVar_hsa_circ_107887,RMVar_hsa_circ_196860,RMVar_hsa_circ_13109,RMVar_hsa_circ_77677,RMVar_hsa_circ_196867,RMVar_hsa_circ_196868,RMVar_hsa_circ_371619,RMVar_hsa_circ_373941,RMVar_hsa_circ_26490,RMVar_hsa_circ_43012,RMVar_hsa_circ_110741,RMVar_hsa_circ_196870,RMVar_hsa_circ_196871,RMVar_hsa_circ_377354,RMVar_hsa_circ_11181,RMVar_hsa_circ_68155,RMVar_hsa_circ_196873,RMVar_hsa_circ_70594,RMVar_hsa_circ_196875,RMVar_hsa_circ_105068,RMVar_hsa_circ_116674,RMVar_hsa_circ_196876,RMVar_hsa_circ_41462,RMVar_hsa_circ_345013,RMVar_hsa_circ_358810,RMVar_hsa_circ_313191,RMVar_hsa_circ_196878 21275 RMVar_ID_21275 Human_SNP_ID_60257985 A-to-I Human chr2 + 9450926 9450926 9450926 AAAACTTAGGGTATGAGGTTTTTGTTGTAAATAGTCGTAGTTACTCCTGAGTCTTACTGTCCACA AAAACTTAGGGTATGAGGTTTTTGTTGTAAATGGTCGTAGTTACTCCTGAGTCTTACTGTCCACA A G CPSF3 Ensembl:ENSG00000119203 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6705033 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_1980,GWAS_ID_1981,GWAS_ID_1982,GWAS_ID_1983 RMVar_hsa_circ_118941,RMVar_hsa_circ_196859,RMVar_hsa_circ_107887,RMVar_hsa_circ_196860,RMVar_hsa_circ_13109,RMVar_hsa_circ_77677,RMVar_hsa_circ_196867,RMVar_hsa_circ_196868,RMVar_hsa_circ_371619,RMVar_hsa_circ_373941,RMVar_hsa_circ_26490,RMVar_hsa_circ_43012,RMVar_hsa_circ_110741,RMVar_hsa_circ_196870,RMVar_hsa_circ_196871,RMVar_hsa_circ_377354,RMVar_hsa_circ_11181,RMVar_hsa_circ_68155,RMVar_hsa_circ_196873,RMVar_hsa_circ_70594,RMVar_hsa_circ_196875,RMVar_hsa_circ_105068,RMVar_hsa_circ_116674,RMVar_hsa_circ_196876,RMVar_hsa_circ_41462,RMVar_hsa_circ_345013,RMVar_hsa_circ_358810,RMVar_hsa_circ_313191,RMVar_hsa_circ_196878 21276 RMVar_ID_21276 Human_SNP_ID_60258116 A-to-I Human chr2 + 9451582 9451582 9451582 GCTCAGGAATTGAAGATCAGCATGGGCAACATAGTGAAACTCCATCTCTACAAAAAATACAAAAA GCTCAGGAATTGAAGATCAGCATGGGCAACATGGTGAAACTCCATCTCTACAAAAAATACAAAAA A G CPSF3 Ensembl:ENSG00000119203 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs933226551 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118941,RMVar_hsa_circ_196859,RMVar_hsa_circ_107887,RMVar_hsa_circ_196860,RMVar_hsa_circ_13109,RMVar_hsa_circ_77677,RMVar_hsa_circ_196867,RMVar_hsa_circ_196868,RMVar_hsa_circ_371619,RMVar_hsa_circ_373941,RMVar_hsa_circ_26490,RMVar_hsa_circ_43012,RMVar_hsa_circ_110741,RMVar_hsa_circ_196870,RMVar_hsa_circ_196871,RMVar_hsa_circ_377354,RMVar_hsa_circ_11181,RMVar_hsa_circ_68155,RMVar_hsa_circ_196873,RMVar_hsa_circ_70594,RMVar_hsa_circ_196875,RMVar_hsa_circ_105068,RMVar_hsa_circ_116674,RMVar_hsa_circ_196876,RMVar_hsa_circ_41462,RMVar_hsa_circ_345013,RMVar_hsa_circ_358810,RMVar_hsa_circ_313191,RMVar_hsa_circ_196878 21277 RMVar_ID_21277 Human_SNP_ID_60267386 A-to-I Human chr2 + 9485547 9485547 9485547 ATGGTGGAGCGCGCCTGTAATCCCAGCTACCCAGGAGGCTGAGGTGTGAGAATCGCTTGAACCCG ATGGTGGAGCGCGCCTGTAATCCCAGCTACCCGGGAGGCTGAGGTGTGAGAATCGCTTGAACCCG A G IAH1 Ensembl:ENSG00000134330 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs911358579 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4643,RMVar_hsa_circ_196884,RMVar_hsa_circ_329261,RMVar_hsa_circ_16227 21278 RMVar_ID_21278 Human_SNP_ID_60275488 A-to-I Human chr2 - 9516365 9516365 9516365 TACAAAGAGGCCGGGCATGGTGGCTCATTCCTATAATCTTCGGCACTTTGGGAGGCCGAGGCAGG TACAAAGAGGCCGGGCATGGTGGCTCATTCCTGTAATCTTCGGCACTTTGGGAGGCCGAGGCAGG T C ADAM17 Ensembl:ENSG00000151694 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs953387750 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25571285 RMVar_hsa_circ_38637,RMVar_hsa_circ_20863,RMVar_hsa_circ_196886,RMVar_hsa_circ_128040,RMVar_hsa_circ_265519,RMVar_hsa_circ_51371,RMVar_hsa_circ_377174,RMVar_hsa_circ_95724,RMVar_hsa_circ_266263,RMVar_hsa_circ_196888,RMVar_hsa_circ_196889,RMVar_hsa_circ_269549,RMVar_hsa_circ_36459,RMVar_hsa_circ_74171,RMVar_hsa_circ_14852,RMVar_hsa_circ_196894,RMVar_hsa_circ_117567,RMVar_hsa_circ_296666,RMVar_hsa_circ_323345,RMVar_hsa_circ_345890,RMVar_hsa_circ_351487,RMVar_hsa_circ_328770,RMVar_hsa_circ_318939,RMVar_hsa_circ_196896,RMVar_hsa_circ_196897,RMVar_hsa_circ_196898,RMVar_hsa_circ_196895,RMVar_hsa_circ_196893 21279 RMVar_ID_21279 Human_SNP_ID_60275577 A-to-I Human chr2 - 9516772 9516772 9516772 ATTAGTATCTGATATACTGATTTTTAATTTTTATTTAATTTTTATTTTTTTTGAGACAGAGTCTT ATTAGTATCTGATATACTGATTTTTAATTTTTTTTTAATTTTTATTTTTTTTGAGACAGAGTCTT T A ADAM17 Ensembl:ENSG00000151694 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1211668840 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6958046 RMVar_hsa_circ_38637,RMVar_hsa_circ_20863,RMVar_hsa_circ_196886,RMVar_hsa_circ_128040,RMVar_hsa_circ_265519,RMVar_hsa_circ_51371,RMVar_hsa_circ_377174,RMVar_hsa_circ_95724,RMVar_hsa_circ_266263,RMVar_hsa_circ_196888,RMVar_hsa_circ_196889,RMVar_hsa_circ_269549,RMVar_hsa_circ_36459,RMVar_hsa_circ_74171,RMVar_hsa_circ_14852,RMVar_hsa_circ_196894,RMVar_hsa_circ_117567,RMVar_hsa_circ_296666,RMVar_hsa_circ_323345,RMVar_hsa_circ_345890,RMVar_hsa_circ_351487,RMVar_hsa_circ_328770,RMVar_hsa_circ_318939,RMVar_hsa_circ_196896,RMVar_hsa_circ_196897,RMVar_hsa_circ_196898,RMVar_hsa_circ_196895,RMVar_hsa_circ_196893 21280 RMVar_ID_21280 Human_SNP_ID_60276134 A-to-I Human chr2 - 9519121 9519120 9519121 GCTGAGGATGAGGCAGTGGATTGTTTGAGCCCAGGAGTTCAAGGCTAGCTTGGGCAACATGTTGT GCTGAGGATGAGGCAGTGGATTGTTTGAGCCC_GGAGTTCAAGGCTAGCTTGGGCAACATGTTGT CT C ADAM17 Ensembl:ENSG00000151694 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1039273703 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_38637,RMVar_hsa_circ_20863,RMVar_hsa_circ_196886,RMVar_hsa_circ_128040,RMVar_hsa_circ_51371,RMVar_hsa_circ_377174,RMVar_hsa_circ_95724,RMVar_hsa_circ_266263,RMVar_hsa_circ_196888,RMVar_hsa_circ_196889,RMVar_hsa_circ_269549,RMVar_hsa_circ_36459,RMVar_hsa_circ_74171,RMVar_hsa_circ_14852,RMVar_hsa_circ_196894,RMVar_hsa_circ_117567,RMVar_hsa_circ_296666,RMVar_hsa_circ_323345,RMVar_hsa_circ_345890,RMVar_hsa_circ_351487,RMVar_hsa_circ_328770,RMVar_hsa_circ_318939,RMVar_hsa_circ_196896,RMVar_hsa_circ_196897,RMVar_hsa_circ_196898,RMVar_hsa_circ_196895,RMVar_hsa_circ_196893,RMVar_hsa_circ_338760,RMVar_hsa_circ_360412,RMVar_hsa_circ_361400,RMVar_hsa_circ_344164,RMVar_hsa_circ_73940,RMVar_hsa_circ_196899,RMVar_hsa_circ_196900 21281 RMVar_ID_21281 Human_SNP_ID_60279291 A-to-I Human chr2 - 9532586 9532586 9532586 ATGCCTGTGGTCTCAGCTACTTAGAATGCTGAAGCAGTAGGATCAGTTGAATTCGGAAGGCGGAG ATGCCTGTGGTCTCAGCTACTTAGAATGCTGAGGCAGTAGGATCAGTTGAATTCGGAAGGCGGAG T C ADAM17 Ensembl:ENSG00000151694 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1337266411 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_377174,RMVar_hsa_circ_196888,RMVar_hsa_circ_36459,RMVar_hsa_circ_117567,RMVar_hsa_circ_323345,RMVar_hsa_circ_345890,RMVar_hsa_circ_196896,RMVar_hsa_circ_196897,RMVar_hsa_circ_196898,RMVar_hsa_circ_338760,RMVar_hsa_circ_361400,RMVar_hsa_circ_64313,RMVar_hsa_circ_196899,RMVar_hsa_circ_196900,RMVar_hsa_circ_311735,RMVar_hsa_circ_341556,RMVar_hsa_circ_196902,RMVar_hsa_circ_295395,RMVar_hsa_circ_68138,RMVar_hsa_circ_350602,RMVar_hsa_circ_299831,RMVar_hsa_circ_196903 21282 RMVar_ID_21282 Human_SNP_ID_60280503 A-to-I Human chr2 - 9537724 9537724 9537724 GAAAAAAAGCACGAGTACTTTTTTTTTTTCTTATTTTGAGCGGGAGTCTCGCGCTGTCAACCAGG GAAAAAAAGCACGAGTACTTTTTTTTTTTCTTTTTTTGAGCGGGAGTCTCGCGCTGTCAACCAGG T A ADAM17 Ensembl:ENSG00000151694 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1157133538 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3640698,Human_RBP_ID_6958188,Human_RBP_ID_18948925 RMVar_hsa_circ_377174,RMVar_hsa_circ_196888,RMVar_hsa_circ_323345,RMVar_hsa_circ_196898,RMVar_hsa_circ_361400,RMVar_hsa_circ_64313,RMVar_hsa_circ_196899,RMVar_hsa_circ_311735,RMVar_hsa_circ_350602,RMVar_hsa_circ_54673,RMVar_hsa_circ_196905,RMVar_hsa_circ_282154,RMVar_hsa_circ_196906 21283 RMVar_ID_21283 Human_SNP_ID_60280504 A-to-I Human chr2 - 9537724 9537724 9537724 GAAAAAAAGCACGAGTACTTTTTTTTTTTCTTATTTTGAGCGGGAGTCTCGCGCTGTCAACCAGG GAAAAAAAGCACGAGTACTTTTTTTTTTTCTTGTTTTGAGCGGGAGTCTCGCGCTGTCAACCAGG T C ADAM17 Ensembl:ENSG00000151694 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1157133538 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3640698,Human_RBP_ID_6958188,Human_RBP_ID_18948925 RMVar_hsa_circ_377174,RMVar_hsa_circ_196888,RMVar_hsa_circ_323345,RMVar_hsa_circ_196898,RMVar_hsa_circ_361400,RMVar_hsa_circ_64313,RMVar_hsa_circ_196899,RMVar_hsa_circ_311735,RMVar_hsa_circ_350602,RMVar_hsa_circ_54673,RMVar_hsa_circ_196905,RMVar_hsa_circ_282154,RMVar_hsa_circ_196906 21284 RMVar_ID_21284 Human_SNP_ID_60283310 A-to-I Human chr2 - 9549361 9549357 9549361 TTTTTGTTTGTTTGTTTTTGAGATGGAGTCTCACTCTATCACCTAGGCTGGAGTGCAGTGGCGTG TTTTTGTTTGTTTGTTTTTGAGATGGAGTCTC____TATCACCTAGGCTGGAGTGCAGTGGCGTG AGAGT A ADAM17 Ensembl:ENSG00000151694 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs781049262 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_196906 21285 RMVar_ID_21285 Human_SNP_ID_60283373 A-to-I Human chr2 - 9549620 9549620 9549620 GGTCCCAGCCACCCGGAGGATTGCTCATGCCCAGGAGGTTGAGGCTGCAGTGAGTGGTGATTGTG GGTCCCAGCCACCCGGAGGATTGCTCATGCCCGGGAGGTTGAGGCTGCAGTGAGTGGTGATTGTG T C ADAM17 Ensembl:ENSG00000151694 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1407524143 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196906 21286 RMVar_ID_21286 Human_SNP_ID_60283643 A-to-I Human chr2 - 9550646 9550646 9550646 GAGGCCAGGAGTTCAAGACCAGCTTGACCAACATGGTGAAACCTGTCTCTACTAAAAATACAAAA GAGGCCAGGAGTTCAAGACCAGCTTGACCAACGTGGTGAAACCTGTCTCTACTAAAAATACAAAA T C ADAM17 Ensembl:ENSG00000151694 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs13030469 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196906 21287 RMVar_ID_21287 Human_SNP_ID_60283659 A-to-I Human chr2 - 9550720 9550720 9550720 GAATGAGTAGCTGGACACAGTGGCTTACACCTATAGTCCCAGCACTTTGGGAGGCTGAGGCCGGC GAATGAGTAGCTGGACACAGTGGCTTACACCTGTAGTCCCAGCACTTTGGGAGGCTGAGGCCGGC T C ADAM17 Ensembl:ENSG00000151694 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs372682185 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196906 21288 RMVar_ID_21288 Human_SNP_ID_60283660 A-to-I Human chr2 - 9550720 9550720 9550720 GAATGAGTAGCTGGACACAGTGGCTTACACCTATAGTCCCAGCACTTTGGGAGGCTGAGGCCGGC GAATGAGTAGCTGGACACAGTGGCTTACACCTCTAGTCCCAGCACTTTGGGAGGCTGAGGCCGGC T G ADAM17 Ensembl:ENSG00000151694 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs372682185 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_196906 21289 RMVar_ID_21289 Human_SNP_ID_60290022 A-to-I Human chr2 + 9575533 9575533 9575533 GGCCAGGAGTTCAAGACCACCCTGGGCAACATAGTGAGACCTTGTCTCTACCCTCCTCCCCAACC GGCCAGGAGTTCAAGACCACCCTGGGCAACATGGTGAGACCTTGTCTCTACCCTCCTCCCCAACC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1358304488 Functional Loss SNV dbSNP153 33..33 33 - - - 21290 RMVar_ID_21290 Human_SNP_ID_60295895 A-to-I Human chr2 - 9597564 9597564 9597564 TGTCTCACTGCAACCCTCTGCCTTTCAGTTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGC TGTCTCACTGCAACCCTCTGCCTTTCAGTTTCGAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGC T C YWHAQ Ensembl:ENSG00000134308 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1402147903 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79062,RMVar_hsa_circ_196910 21291 RMVar_ID_21291 Human_SNP_ID_60296934 A-to-I Human chr2 - 9601373 9601373 9601373 CTCACTGCAACCTCTGCCTCCTGGGTTCAAGCAGTTCTGCCTCAGCCTCCCGAGTAGCTGGGATT CTCACTGCAACCTCTGCCTCCTGGGTTCAAGCGGTTCTGCCTCAGCCTCCCGAGTAGCTGGGATT T C YWHAQ Ensembl:ENSG00000134308 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs980970418 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79062,RMVar_hsa_circ_196910 21292 RMVar_ID_21292 Human_SNP_ID_60297813 A-to-I Human chr2 - 9603741 9603740 9603741 TTTTAGTATTTTTAATAGAGGGGAGTTTCACCATGCTAGCCAGGCTGCTCTCGAACTCCTGACCG TTTTAGTATTTTTAATAGAGGGGAGTTTCACC_TGCTAGCCAGGCTGCTCTCGAACTCCTGACCG AT A YWHAQ Ensembl:ENSG00000134308 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs71389268 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_79062,RMVar_hsa_circ_196910 21293 RMVar_ID_21293 Human_SNP_ID_60297854 A-to-I Human chr2 - 9603868 9603868 9603868 CAGGCTGGAGTGCAGTGGCGTGATCTCAGCTCACTGTGACCTCCTCCTCCTGGGTTAAAGAGATT CAGGCTGGAGTGCAGTGGCGTGATCTCAGCTCGCTGTGACCTCCTCCTCCTGGGTTAAAGAGATT T C YWHAQ Ensembl:ENSG00000134308 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs966224515 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79062,RMVar_hsa_circ_196910 21294 RMVar_ID_21294 Human_SNP_ID_60361709 A-to-I Human chr2 + 9852025 9852025 9852025 TTTGAGAACAAAATCGTTTGGTGTATGTACATAACGTCCATCAGGACTTGAGTTCCACAGAATGC TTTGAGAACAAAATCGTTTGGTGTATGTACATGACGTCCATCAGGACTTGAGTTCCACAGAATGC A G TAF1B Ensembl:ENSG00000115750 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1157989659 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1024710 Human_Splice_Rec_217060,Human_Splice_Rec_217124 RMVar_hsa_circ_8469,RMVar_hsa_circ_16824,RMVar_hsa_circ_360092,RMVar_hsa_circ_370697,RMVar_hsa_circ_277698,RMVar_hsa_circ_50264,RMVar_hsa_circ_40124,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_196915 21295 RMVar_ID_21295 Human_SNP_ID_60361713 A-to-I Human chr2 + 9852035 9852035 9852035 AAATCGTTTGGTGTATGTACATAACGTCCATCAGGACTTGAGTTCCACAGAATGCACTTTGGACA AAATCGTTTGGTGTATGTACATAACGTCCATCGGGACTTGAGTTCCACAGAATGCACTTTGGACA A G TAF1B Ensembl:ENSG00000115750 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1012661525 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1024710 Human_Splice_Rec_217060,Human_Splice_Rec_217124 RMVar_hsa_circ_8469,RMVar_hsa_circ_16824,RMVar_hsa_circ_360092,RMVar_hsa_circ_370697,RMVar_hsa_circ_277698,RMVar_hsa_circ_50264,RMVar_hsa_circ_40124,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_196915 21296 RMVar_ID_21296 Human_SNP_ID_60381789 A-to-I Human chr2 + 9934562 9934562 9934562 TTAGTTTTCTGAGGCCGGGCGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGT TTAGTTTTCTGAGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs373919701 Functional Loss SNV dbSNP153 33..33 33 - - - 21297 RMVar_ID_21297 Human_SNP_ID_60382213 A-to-I Human chr2 + 9935792 9935792 9935792 ACAGGGTCTTGCTGTGTCACCCAGGCTGGAGTACAGTGGTGTGACCTTGGCTCACTGCAGCTTTG ACAGGGTCTTGCTGTGTCACCCAGGCTGGAGTGCAGTGGTGTGACCTTGGCTCACTGCAGCTTTG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1398031623 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6808261 21298 RMVar_ID_21298 Human_SNP_ID_60382322 A-to-I Human chr2 + 9936125 9936125 9936125 TCACTCTGTCGCCCAGGCTGGAGTGCAGTGGCACGATCTCGGCTCACTGCAAGCCCCGCCTCCCG TCACTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCGATCTCGGCTCACTGCAAGCCCCGCCTCCCG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928535601 Functional Loss SNV dbSNP153 33..33 33 - - - 21299 RMVar_ID_21299 Human_SNP_ID_60382333 A-to-I Human chr2 + 9936138 9936138 9936138 CAGGCTGGAGTGCAGTGGCACGATCTCGGCTCACTGCAAGCCCCGCCTCCCGGCTTCATGCCATT CAGGCTGGAGTGCAGTGGCACGATCTCGGCTCGCTGCAAGCCCCGCCTCCCGGCTTCATGCCATT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1047836491 Functional Loss SNV dbSNP153 33..33 33 - - - 21300 RMVar_ID_21300 Human_SNP_ID_60382504 A-to-I Human chr2 + 9936332 9936332 9936332 CACCCGCCTTGGCCTCCTAAAGTGCTGGGATTACAGGCGTGAGCCACCGTGCCCAGCCTAATTTT CACCCGCCTTGGCCTCCTAAAGTGCTGGGATTGCAGGCGTGAGCCACCGTGCCCAGCCTAATTTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1381264676 Functional Loss SNV dbSNP153 33..33 33 - - - 21301 RMVar_ID_21301 Human_SNP_ID_60382629 A-to-I Human chr2 + 9936698 9936698 9936698 ACCTCAGGTGATCCTCCCACCTCTGTCTCCCAAAGTGCTGGAATTACAGATGTGAGCCACTGCGC ACCTCAGGTGATCCTCCCACCTCTGTCTCCCAGAGTGCTGGAATTACAGATGTGAGCCACTGCGC A G AC010969.2 Ensembl:ENSG00000269973 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1239221120 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5249259,Human_RBP_ID_8201372 21302 RMVar_ID_21302 Human_SNP_ID_60415446 A-to-I Human chr2 + 10050588 10050588 10050588 AAAAATAGTTGGGCTTGGTGGCACGCTCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA AAAAATAGTTGGGCTTGGTGGCACGCTCCTGTGGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA A G KLF11 Ensembl:ENSG00000172059 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1172686770 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_147593 21303 RMVar_ID_21303 Human_SNP_ID_60415448 A-to-I Human chr2 + 10050598 10050598 10050598 GGGCTTGGTGGCACGCTCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAG GGGCTTGGTGGCACGCTCCTGTAGTCCCAGCTGCTTGGGAGGCTGAGGCAGGAGAATCGCTTGAG A G KLF11 Ensembl:ENSG00000172059 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992944959 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_147593 21304 RMVar_ID_21304 Human_SNP_ID_60415449 A-to-I Human chr2 + 10050598 10050598 10050598 GGGCTTGGTGGCACGCTCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAG GGGCTTGGTGGCACGCTCCTGTAGTCCCAGCTTCTTGGGAGGCTGAGGCAGGAGAATCGCTTGAG A T KLF11 Ensembl:ENSG00000172059 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992944959 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_147593 21305 RMVar_ID_21305 Human_SNP_ID_60415883 A-to-I Human chr2 + 10051724 10051724 10051724 TATTTTTAGTAGAGATGGGGTTTCACCGTGTTAGCCAGGATGGTCTCGGTCTTCTGACTTTGTGA TATTTTTAGTAGAGATGGGGTTTCACCGTGTTGGCCAGGATGGTCTCGGTCTTCTGACTTTGTGA A G KLF11 Ensembl:ENSG00000172059 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs577872304 Functional Loss SNV dbSNP153 33..33 33 - - - 21306 RMVar_ID_21306 Human_SNP_ID_60420654 A-to-I Human chr2 - 10069497 10069497 10069497 GGGCGTGGTGGCACGCACCTGTGGTCCCAGCTACTCGGGAGTCTGAGGCAGGAGAATCGCTTGAA GGGCGTGGTGGCACGCACCTGTGGTCCCAGCTGCTCGGGAGTCTGAGGCAGGAGAATCGCTTGAA T C CYS1 Ensembl:ENSG00000205795 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1160624597 Functional Loss SNV dbSNP153 33..33 33 - - - 21307 RMVar_ID_21307 Human_SNP_ID_60434496 A-to-I Human chr2 - 10119972 10119972 10119972 GCCTCAACTATCCGAGCTCAAGCGATCCTCCCACCTCAGCCTCCCGAGTAGCTGGGACTCAAGGC GCCTCAACTATCCGAGCTCAAGCGATCCTCCCTCCTCAGCCTCCCGAGTAGCTGGGACTCAAGGC T A lnc-CYS1-9,lnc-CYS1-9:2 RNACentral:URS0000D595CB,RNACentral:URS0000D5741A lincRNA,lincRNA exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1166617705 Functional Loss SNV dbSNP153 33..33 33 - - - 21308 RMVar_ID_21308 Human_SNP_ID_60434523 A-to-I Human chr2 - 10120054 10120054 10120054 CTGTTTGAGTTTTTTGTTTTTTGTTTTGAGACAGGGTCTTGCTCTGTTGCCCAGTCTGGTGGCTC CTGTTTGAGTTTTTTGTTTTTTGTTTTGAGACCGGGTCTTGCTCTGTTGCCCAGTCTGGTGGCTC T G lnc-CYS1-9,lnc-CYS1-9:2 RNACentral:URS0000D595CB,RNACentral:URS0000D5741A lincRNA,lincRNA exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs995434696 Functional Loss SNV dbSNP153 33..33 33 - - - 21309 RMVar_ID_21309 Human_SNP_ID_60437007 A-to-I Human chr2 + 10128120 10128118 10128120 CTGGGAGGTGGAGGTTGCAGTGAGTCAAGATCACACCACTGCACTCCAGCCTGGGTGACAGTCCC CTGGGAGGTGGAGGTTGCAGTGAGTCAAGAT__CACCACTGCACTCCAGCCTGGGTGACAGTCCC TCA T RRM2 Ensembl:ENSG00000171848 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1263724166 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_12142,RMVar_hsa_circ_65270,RMVar_hsa_circ_371954,RMVar_hsa_circ_196929,RMVar_hsa_circ_106923,RMVar_hsa_circ_18516,RMVar_hsa_circ_117641,RMVar_hsa_circ_196933,RMVar_hsa_circ_196934 21310 RMVar_ID_21310 Human_SNP_ID_60437115 A-to-I Human chr2 + 10128671 10128671 10128671 AGGGTCTTGAATGGGACTGAGCTTGCCTTGGTAGTGACATCAGCAGAGAAGTCAGTAGTTGAAGT AGGGTCTTGAATGGGACTGAGCTTGCCTTGGTGGTGACATCAGCAGAGAAGTCAGTAGTTGAAGT A G RRM2 Ensembl:ENSG00000171848 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4668664 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_1984,GWAS_ID_1985,GWAS_ID_1986,GWAS_ID_1987 RMVar_hsa_circ_12142,RMVar_hsa_circ_65270,RMVar_hsa_circ_371954,RMVar_hsa_circ_196929,RMVar_hsa_circ_106923,RMVar_hsa_circ_18516,RMVar_hsa_circ_117641,RMVar_hsa_circ_196933,RMVar_hsa_circ_196934 21311 RMVar_ID_21311 Human_SNP_ID_60437802 A-to-I Human chr2 + 10131696 10131696 10131696 GGGAGGCAGAGGTTGCAGTGAGCTGAGATTGCACCGCTGCACTCCAGCCTGGGCAGCAGAGTGAG GGGAGGCAGAGGTTGCAGTGAGCTGAGATTGCGCCGCTGCACTCCAGCCTGGGCAGCAGAGTGAG A G RRM2 Ensembl:ENSG00000171848 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1212483963 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_65270 21312 RMVar_ID_21312 Human_SNP_ID_60441128 A-to-I Human chr2 + 10144547 10144547 10144547 TTGGGTCCAGCAGCTTTCTCAGTCCCAAACACATGTGACCTCACGATTCTGGCCCTTCCATGATC TTGGGTCCAGCAGCTTTCTCAGTCCCAAACACGTGTGACCTCACGATTCTGGCCCTTCCATGATC A G RRM2 Ensembl:ENSG00000171848 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs12692399 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1097685,Human_RBP_ID_14002199,Human_RBP_ID_18493174 21313 RMVar_ID_21313 Human_SNP_ID_60441129 A-to-I Human chr2 + 10144547 10144547 10144547 TTGGGTCCAGCAGCTTTCTCAGTCCCAAACACATGTGACCTCACGATTCTGGCCCTTCCATGATC TTGGGTCCAGCAGCTTTCTCAGTCCCAAACACTTGTGACCTCACGATTCTGGCCCTTCCATGATC A T RRM2 Ensembl:ENSG00000171848 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs12692399 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1097685,Human_RBP_ID_14002199,Human_RBP_ID_18493174 21314 RMVar_ID_21314 Human_SNP_ID_60441757 A-to-I Human chr2 + 10147150 10147150 10147150 AATTTTTGCATTTTTAGTAGACATGGGGTTTCACCTTGTTGGCCAGGATGGACTTGATCTCTCGA AATTTTTGCATTTTTAGTAGACATGGGGTTTCGCCTTGTTGGCCAGGATGGACTTGATCTCTCGA A G RRM2 Ensembl:ENSG00000171848 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1374596639 Functional Loss SNV dbSNP153 33..33 33 - - - 21315 RMVar_ID_21315 Human_SNP_ID_60455508 A-to-I Human chr2 + 10200094 10200094 10200094 ACCTCAGGTGATCCACCCATGTCAGCCTCCCAAAGTGCTGGGATTACAGAAGTGAACCACCGCAC ACCTCAGGTGATCCACCCATGTCAGCCTCCCAGAGTGCTGGGATTACAGAAGTGAACCACCGCAC A G RRM2 Ensembl:ENSG00000171848 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1010560915 Functional Loss SNV dbSNP153 33..33 33 - - - 21316 RMVar_ID_21316 Human_SNP_ID_60458761 A-to-I Human chr2 + 10212868 10212868 10212868 GGAAACCCTGTGTCTACAAAAATACAAAAATTAGCTAGGCGTAGTGGCACATGCCTGTAGTCCCA GGAAACCCTGTGTCTACAAAAATACAAAAATTGGCTAGGCGTAGTGGCACATGCCTGTAGTCCCA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs746014753 Functional Loss SNV dbSNP153 33..33 33 - - - 21317 RMVar_ID_21317 Human_SNP_ID_60484844 A-to-I Human chr2 + 10308931 10308931 10308931 AACAAAACAAATCTATTTTCTAAGCCAGGCACAGTGGCTCTTGTCTGTAGTTCCAGCTACTAGGG AACAAAACAAATCTATTTTCTAAGCCAGGCACGGTGGCTCTTGTCTGTAGTTCCAGCTACTAGGG A G HPCAL1 Ensembl:ENSG00000115756 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054154971 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100523,RMVar_hsa_circ_196942 21318 RMVar_ID_21318 Human_SNP_ID_60484845 A-to-I Human chr2 + 10308931 10308931 10308931 AACAAAACAAATCTATTTTCTAAGCCAGGCACAGTGGCTCTTGTCTGTAGTTCCAGCTACTAGGG AACAAAACAAATCTATTTTCTAAGCCAGGCACTGTGGCTCTTGTCTGTAGTTCCAGCTACTAGGG A T HPCAL1 Ensembl:ENSG00000115756 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054154971 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100523,RMVar_hsa_circ_196942 21319 RMVar_ID_21319 Human_SNP_ID_60484896 A-to-I Human chr2 + 10309168 10309168 10309168 GCAATCCCCCTGCCATAGTCTCCTGAGTAGCTAGGACTACAGGTACACACCACCATGCCTGCTGA GCAATCCCCCTGCCATAGTCTCCTGAGTAGCTGGGACTACAGGTACACACCACCATGCCTGCTGA A G HPCAL1 Ensembl:ENSG00000115756 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1024977816 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100523,RMVar_hsa_circ_196942 21320 RMVar_ID_21320 Human_SNP_ID_60487690 A-to-I Human chr2 + 10321002 10321002 10321002 GATGGAAGAGCGTGAGTGTATTAGGCCGTTCCACATTGTTATAAAGAAATACCTGAGACACGGTC GATGGAAGAGCGTGAGTGTATTAGGCCGTTCCTCATTGTTATAAAGAAATACCTGAGACACGGTC A T HPCAL1 Ensembl:ENSG00000115756 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355845712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2575713 RMVar_hsa_circ_100523,RMVar_hsa_circ_196942 21321 RMVar_ID_21321 Human_SNP_ID_60491053 A-to-I Human chr2 + 10334779 10334779 10334779 ACGATCTCGGCTCATTGCAACTTCCACCTCCCAGGCTCAAGCAATCTTCCCACCTCAGCCTCCCA ACGATCTCGGCTCATTGCAACTTCCACCTCCCGGGCTCAAGCAATCTTCCCACCTCAGCCTCCCA A G HPCAL1 Ensembl:ENSG00000115756 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1322329171 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100523,RMVar_hsa_circ_196942 21322 RMVar_ID_21322 Human_SNP_ID_60566948 A-to-I Human chr2 - 10621486 10621486 10621486 GGGTTCAAGTGATTCCCCAACCTCAGTCTCCCAAGTACCCAGGACTACAGGAATGTGCCACCACA GGGTTCAAGTGATTCCCCAACCTCAGTCTCCCGAGTACCCAGGACTACAGGAATGTGCCACCACA T C NOL10 Ensembl:ENSG00000115761 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1396345144 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_196972,RMVar_hsa_circ_196973,RMVar_hsa_circ_196974 21323 RMVar_ID_21323 Human_SNP_ID_60573351 A-to-I Human chr2 - 10645824 10645824 10645824 AGACGTGGTTTTGGTAAGATAGTATCGAGGCCAGATGCGGTGGCTCATGCCTGTAATCCCAGCAT AGACGTGGTTTTGGTAAGATAGTATCGAGGCCGGATGCGGTGGCTCATGCCTGTAATCCCAGCAT T C NOL10 Ensembl:ENSG00000115761 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1377054014 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_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_117870,RMVar_hsa_circ_196975,RMVar_hsa_circ_196973,RMVar_hsa_circ_196977,RMVar_hsa_circ_196974,RMVar_hsa_circ_196976,RMVar_hsa_circ_307986,RMVar_hsa_circ_196979,RMVar_hsa_circ_336499,RMVar_hsa_circ_318379,RMVar_hsa_circ_281998,RMVar_hsa_circ_286973,RMVar_hsa_circ_272543,RMVar_hsa_circ_196982,RMVar_hsa_circ_196984,RMVar_hsa_circ_196985,RMVar_hsa_circ_196986,RMVar_hsa_circ_196983,RMVar_hsa_circ_196981 21324 RMVar_ID_21324 Human_SNP_ID_60577738 A-to-I Human chr2 - 10662978 10662978 10662978 ACAGAGTTGGCCTGTTAGACTGCGCCTTAAACAGTGTCACAGCAGATTCAGAGTAAGTAGAAATT ACAGAGTTGGCCTGTTAGACTGCGCCTTAAACGGTGTCACAGCAGATTCAGAGTAAGTAGAAATT T C NOL10 Ensembl:ENSG00000115761 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs201462244 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_1895025,Human_RBP_ID_3957601,Human_RBP_ID_13570290,Human_RBP_ID_18998930,Human_RBP_ID_19099281 Human_Splice_Rec_217672,Human_Splice_Rec_217673,Human_Splice_Rec_217712,Human_Splice_Rec_217713,Human_Splice_Rec_217748,Human_Splice_Rec_217749,Human_Splice_Rec_217778,Human_Splice_Rec_217779 RMVar_hsa_circ_47263,RMVar_hsa_circ_196964,RMVar_hsa_circ_348261,RMVar_hsa_circ_61610,RMVar_hsa_circ_67183,RMVar_hsa_circ_51498,RMVar_hsa_circ_1773,RMVar_hsa_circ_196968,RMVar_hsa_circ_362737,RMVar_hsa_circ_94451,RMVar_hsa_circ_117870,RMVar_hsa_circ_196973,RMVar_hsa_circ_196977,RMVar_hsa_circ_196976,RMVar_hsa_circ_336499,RMVar_hsa_circ_286973,RMVar_hsa_circ_272543,RMVar_hsa_circ_31475,RMVar_hsa_circ_196982,RMVar_hsa_circ_196984,RMVar_hsa_circ_196983,RMVar_hsa_circ_333690,RMVar_hsa_circ_196981,RMVar_hsa_circ_293414,RMVar_hsa_circ_51472,RMVar_hsa_circ_196987,RMVar_hsa_circ_196988,RMVar_hsa_circ_196989,RMVar_hsa_circ_311380,RMVar_hsa_circ_295924,RMVar_hsa_circ_114714,RMVar_hsa_circ_310521,RMVar_hsa_circ_196990,RMVar_hsa_circ_301232,RMVar_hsa_circ_58317,RMVar_hsa_circ_196991,RMVar_hsa_circ_196992 21325 RMVar_ID_21325 Human_SNP_ID_60581880 A-to-I Human chr2 - 10678327 10678327 10678327 AAAAACAGCAGGGTACACAGTAGCTCATGCCTATAATCCCTGCACTTTGGGAGGCTGAGGCAGGA AAAAACAGCAGGGTACACAGTAGCTCATGCCTGTAATCCCTGCACTTTGGGAGGCTGAGGCAGGA T C NOL10 Ensembl:ENSG00000115761 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs565221670 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_31475,RMVar_hsa_circ_58317,RMVar_hsa_circ_298125,RMVar_hsa_circ_9204,RMVar_hsa_circ_196994,RMVar_hsa_circ_305793,RMVar_hsa_circ_329011,RMVar_hsa_circ_298612,RMVar_hsa_circ_272747 21326 RMVar_ID_21326 Human_SNP_ID_60581881 A-to-I Human chr2 - 10678327 10678327 10678327 AAAAACAGCAGGGTACACAGTAGCTCATGCCTATAATCCCTGCACTTTGGGAGGCTGAGGCAGGA AAAAACAGCAGGGTACACAGTAGCTCATGCCTCTAATCCCTGCACTTTGGGAGGCTGAGGCAGGA T G NOL10 Ensembl:ENSG00000115761 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs565221670 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_31475,RMVar_hsa_circ_58317,RMVar_hsa_circ_298125,RMVar_hsa_circ_9204,RMVar_hsa_circ_196994,RMVar_hsa_circ_305793,RMVar_hsa_circ_329011,RMVar_hsa_circ_298612,RMVar_hsa_circ_272747 21327 RMVar_ID_21327 Human_SNP_ID_60611051 A-to-I Human chr2 - 10785980 10785980 10785980 GCTGGGTGCGGTGGCTCACGCCTGTAATTCCAACACTTTGGGAGTCTGAGGCAGGCGGATCACTT GCTGGGTGCGGTGGCTCACGCCTGTAATTCCAGCACTTTGGGAGTCTGAGGCAGGCGGATCACTT T C PDIA6 Ensembl:ENSG00000143870 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1247244590 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1671,RMVar_hsa_circ_292244,RMVar_hsa_circ_330796,RMVar_hsa_circ_348303 21328 RMVar_ID_21328 Human_SNP_ID_60611053 A-to-I Human chr2 - 10785986 10785986 10785986 TGTGGGGCTGGGTGCGGTGGCTCACGCCTGTAATTCCAACACTTTGGGAGTCTGAGGCAGGCGGA TGTGGGGCTGGGTGCGGTGGCTCACGCCTGTATTTCCAACACTTTGGGAGTCTGAGGCAGGCGGA T A PDIA6 Ensembl:ENSG00000143870 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs372073419 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1671,RMVar_hsa_circ_292244,RMVar_hsa_circ_330796,RMVar_hsa_circ_348303 21329 RMVar_ID_21329 Human_SNP_ID_60611122 A-to-I Human chr2 - 10786120 10786120 10786120 TGGGTTTTCACCAGGTTGGCCAGGCGGGTCTCAAACCCCTGACCTCAAGTGATCCACCCACCTCA TGGGTTTTCACCAGGTTGGCCAGGCGGGTCTCGAACCCCTGACCTCAAGTGATCCACCCACCTCA T C PDIA6 Ensembl:ENSG00000143870 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1464492106 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1671,RMVar_hsa_circ_292244,RMVar_hsa_circ_330796,RMVar_hsa_circ_348303 21330 RMVar_ID_21330 Human_SNP_ID_60613979 A-to-I Human chr2 - 10796104 10796104 10796104 GCTTGCAGTGAGCCGAGATTGTACTCCAGCCTAGGCGACAGAGCGAGACTCCGTCTCAAAAAAAA GCTTGCAGTGAGCCGAGATTGTACTCCAGCCTGGGCGACAGAGCGAGACTCCGTCTCAAAAAAAA T C PDIA6 Ensembl:ENSG00000143870 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs964335078 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_348303,RMVar_hsa_circ_336161,RMVar_hsa_circ_379037,RMVar_hsa_circ_267370,RMVar_hsa_circ_316864,RMVar_hsa_circ_294503,RMVar_hsa_circ_197001,RMVar_hsa_circ_62230 21331 RMVar_ID_21331 Human_SNP_ID_60614008 A-to-I Human chr2 - 10796182 10796182 10796182 GGGCACGGTGGTGGGTGACTGTAGTCCCAGCTACTCTGGAGGCTGAGGCAGGAGAATGGCGTGAA GGGCACGGTGGTGGGTGACTGTAGTCCCAGCTGCTCTGGAGGCTGAGGCAGGAGAATGGCGTGAA T C PDIA6 Ensembl:ENSG00000143870 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1362385923 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_143731 RMVar_hsa_circ_348303,RMVar_hsa_circ_336161,RMVar_hsa_circ_379037,RMVar_hsa_circ_267370,RMVar_hsa_circ_316864,RMVar_hsa_circ_294503,RMVar_hsa_circ_197001,RMVar_hsa_circ_62230 21332 RMVar_ID_21332 Human_SNP_ID_60692624 A-to-I Human chr2 - 11099995 11099995 11099995 GGTTAGGGAAGATCCTGCTCCTGGAAGGAGAAAGATGTGGAGTGGAGAAAATCTCAGCCACCAGG GGTTAGGGAAGATCCTGCTCCTGGAAGGAGAAGGATGTGGAGTGGAGAAAATCTCAGCCACCAGG T C FLJ33534,FLJ33534:2 RNACentral:URS0000759C02,RNACentral:URS00008BBF47 lincRNA,lincRNA exon,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1415480552 Functional Loss SNV dbSNP153 33..33 33 - - - 21333 RMVar_ID_21333 Human_SNP_ID_60717203 A-to-I Human chr2 - 11188949 11188949 11188949 CACCCTAACCCTCCACCTTCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTTCTGGGTAGTTGGGA CACCCTAACCCTCCACCTTCCAGGTTCAAGCAGTTCTCCTGCCTCAGCCTTCTGGGTAGTTGGGA T C ROCK2 Ensembl:ENSG00000134318 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1020448827 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90854,RMVar_hsa_circ_115102,RMVar_hsa_circ_119717,RMVar_hsa_circ_125089,RMVar_hsa_circ_128041,RMVar_hsa_circ_121704,RMVar_hsa_circ_117959,RMVar_hsa_circ_118867,RMVar_hsa_circ_116666,RMVar_hsa_circ_102916,RMVar_hsa_circ_113128,RMVar_hsa_circ_113994,RMVar_hsa_circ_97617,RMVar_hsa_circ_99322,RMVar_hsa_circ_93716,RMVar_hsa_circ_197010,RMVar_hsa_circ_197018,RMVar_hsa_circ_77214,RMVar_hsa_circ_82417,RMVar_hsa_circ_83388,RMVar_hsa_circ_81318,RMVar_hsa_circ_197020,RMVar_hsa_circ_197022,RMVar_hsa_circ_197024,RMVar_hsa_circ_197023,RMVar_hsa_circ_197021,RMVar_hsa_circ_197019,RMVar_hsa_circ_197014,RMVar_hsa_circ_197016,RMVar_hsa_circ_197017,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 21334 RMVar_ID_21334 Human_SNP_ID_60717207 A-to-I Human chr2 - 11188960 11188960 11188960 TGATCTCGGTTCACCCTAACCCTCCACCTTCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTTCTG TGATCTCGGTTCACCCTAACCCTCCACCTTCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTTCTG T C ROCK2 Ensembl:ENSG00000134318 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs747699007 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90854,RMVar_hsa_circ_115102,RMVar_hsa_circ_119717,RMVar_hsa_circ_125089,RMVar_hsa_circ_128041,RMVar_hsa_circ_121704,RMVar_hsa_circ_117959,RMVar_hsa_circ_118867,RMVar_hsa_circ_116666,RMVar_hsa_circ_102916,RMVar_hsa_circ_113128,RMVar_hsa_circ_113994,RMVar_hsa_circ_97617,RMVar_hsa_circ_99322,RMVar_hsa_circ_93716,RMVar_hsa_circ_197010,RMVar_hsa_circ_197018,RMVar_hsa_circ_77214,RMVar_hsa_circ_82417,RMVar_hsa_circ_83388,RMVar_hsa_circ_81318,RMVar_hsa_circ_197020,RMVar_hsa_circ_197022,RMVar_hsa_circ_197024,RMVar_hsa_circ_197023,RMVar_hsa_circ_197021,RMVar_hsa_circ_197019,RMVar_hsa_circ_197014,RMVar_hsa_circ_197016,RMVar_hsa_circ_197017,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 21335 RMVar_ID_21335 Human_SNP_ID_60717228 A-to-I Human chr2 - 11189011 11189011 11189011 TTTTTGTGACATGACGTCTCACTCTGTCACCCAGGCTGGAGTGTAGTGGCGTGATCTCGGTTCAC TTTTTGTGACATGACGTCTCACTCTGTCACCCGGGCTGGAGTGTAGTGGCGTGATCTCGGTTCAC T C ROCK2 Ensembl:ENSG00000134318 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs953405998 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13581132 RMVar_hsa_circ_90854,RMVar_hsa_circ_115102,RMVar_hsa_circ_119717,RMVar_hsa_circ_125089,RMVar_hsa_circ_128041,RMVar_hsa_circ_121704,RMVar_hsa_circ_117959,RMVar_hsa_circ_118867,RMVar_hsa_circ_116666,RMVar_hsa_circ_102916,RMVar_hsa_circ_113128,RMVar_hsa_circ_113994,RMVar_hsa_circ_97617,RMVar_hsa_circ_99322,RMVar_hsa_circ_93716,RMVar_hsa_circ_197010,RMVar_hsa_circ_197018,RMVar_hsa_circ_77214,RMVar_hsa_circ_82417,RMVar_hsa_circ_83388,RMVar_hsa_circ_81318,RMVar_hsa_circ_197020,RMVar_hsa_circ_197022,RMVar_hsa_circ_197024,RMVar_hsa_circ_197023,RMVar_hsa_circ_197021,RMVar_hsa_circ_197019,RMVar_hsa_circ_197014,RMVar_hsa_circ_197016,RMVar_hsa_circ_197017,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 21336 RMVar_ID_21336 Human_SNP_ID_60717397 A-to-I Human chr2 - 11189799 11189799 11189799 TTTTTATTTTCTGTAGAGATGGGGGTCTCCCTATGTTGCCCAGGCTGGTCTCAAATGCCTGGCCT TTTTTATTTTCTGTAGAGATGGGGGTCTCCCTGTGTTGCCCAGGCTGGTCTCAAATGCCTGGCCT T C ROCK2 Ensembl:ENSG00000134318 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs544383361 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22980995 RMVar_hsa_circ_90854,RMVar_hsa_circ_115102,RMVar_hsa_circ_119717,RMVar_hsa_circ_125089,RMVar_hsa_circ_128041,RMVar_hsa_circ_121704,RMVar_hsa_circ_117959,RMVar_hsa_circ_118867,RMVar_hsa_circ_116666,RMVar_hsa_circ_102916,RMVar_hsa_circ_113128,RMVar_hsa_circ_113994,RMVar_hsa_circ_97617,RMVar_hsa_circ_99322,RMVar_hsa_circ_93716,RMVar_hsa_circ_197010,RMVar_hsa_circ_197018,RMVar_hsa_circ_77214,RMVar_hsa_circ_82417,RMVar_hsa_circ_83388,RMVar_hsa_circ_81318,RMVar_hsa_circ_197020,RMVar_hsa_circ_197022,RMVar_hsa_circ_197024,RMVar_hsa_circ_197023,RMVar_hsa_circ_197021,RMVar_hsa_circ_197019,RMVar_hsa_circ_197014,RMVar_hsa_circ_197016,RMVar_hsa_circ_197017,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 21337 RMVar_ID_21337 Human_SNP_ID_60717414 A-to-I Human chr2 - 11189865 11189865 11189865 ACCTCAGCCTCCCAGAGTAGGTGGGACCACATACATGCACCATGACACCTGGCTAATTTTTTTTT ACCTCAGCCTCCCAGAGTAGGTGGGACCACATGCATGCACCATGACACCTGGCTAATTTTTTTTT T C ROCK2 Ensembl:ENSG00000134318 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1216260005 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569401 RMVar_hsa_circ_90854,RMVar_hsa_circ_115102,RMVar_hsa_circ_119717,RMVar_hsa_circ_125089,RMVar_hsa_circ_128041,RMVar_hsa_circ_121704,RMVar_hsa_circ_117959,RMVar_hsa_circ_118867,RMVar_hsa_circ_116666,RMVar_hsa_circ_102916,RMVar_hsa_circ_113128,RMVar_hsa_circ_113994,RMVar_hsa_circ_97617,RMVar_hsa_circ_99322,RMVar_hsa_circ_93716,RMVar_hsa_circ_197010,RMVar_hsa_circ_197018,RMVar_hsa_circ_77214,RMVar_hsa_circ_82417,RMVar_hsa_circ_83388,RMVar_hsa_circ_81318,RMVar_hsa_circ_197020,RMVar_hsa_circ_197022,RMVar_hsa_circ_197024,RMVar_hsa_circ_197023,RMVar_hsa_circ_197021,RMVar_hsa_circ_197019,RMVar_hsa_circ_197014,RMVar_hsa_circ_197016,RMVar_hsa_circ_197017,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 21338 RMVar_ID_21338 Human_SNP_ID_60724465 A-to-I Human chr2 - 11219949 11219949 11219949 CCCAGGTACTCAGAGGCTGAGATGAAAGGATCACTTGAGGCCAGGAGTTCAAGGTTGGAATGAGC CCCAGGTACTCAGAGGCTGAGATGAAAGGATCGCTTGAGGCCAGGAGTTCAAGGTTGGAATGAGC T C ROCK2 Ensembl:ENSG00000134318 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs538426265 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5250,RMVar_hsa_circ_52352,RMVar_hsa_circ_115102,RMVar_hsa_circ_128041,RMVar_hsa_circ_113994,RMVar_hsa_circ_99322,RMVar_hsa_circ_93716,RMVar_hsa_circ_197010,RMVar_hsa_circ_77214,RMVar_hsa_circ_83388,RMVar_hsa_circ_197012,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_94695,RMVar_hsa_circ_117132,RMVar_hsa_circ_66754,RMVar_hsa_circ_197031,RMVar_hsa_circ_358841,RMVar_hsa_circ_197032,RMVar_hsa_circ_64319,RMVar_hsa_circ_61039,RMVar_hsa_circ_44496,RMVar_hsa_circ_12182,RMVar_hsa_circ_307909,RMVar_hsa_circ_35679,RMVar_hsa_circ_197037,RMVar_hsa_circ_73093,RMVar_hsa_circ_48851,RMVar_hsa_circ_341437,RMVar_hsa_circ_36628,RMVar_hsa_circ_55033,RMVar_hsa_circ_12596,RMVar_hsa_circ_197040,RMVar_hsa_circ_59244,RMVar_hsa_circ_335305,RMVar_hsa_circ_64835,RMVar_hsa_circ_197042,RMVar_hsa_circ_291848 21339 RMVar_ID_21339 Human_SNP_ID_60731033 A-to-I Human chr2 - 11248626 11248626 11248626 CTGTTCATTCCATCCTCTGCTTCCCGGGTTCAAGCGGTTCTCCTGCCTCAGTCTCTCGAATAGCT CTGTTCATTCCATCCTCTGCTTCCCGGGTTCAGGCGGTTCTCCTGCCTCAGTCTCTCGAATAGCT T C ROCK2 Ensembl:ENSG00000134318 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1399560948 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113994,RMVar_hsa_circ_93716,RMVar_hsa_circ_77214,RMVar_hsa_circ_197006,RMVar_hsa_circ_197008,RMVar_hsa_circ_197007,RMVar_hsa_circ_94695,RMVar_hsa_circ_66754,RMVar_hsa_circ_197031,RMVar_hsa_circ_64319,RMVar_hsa_circ_12182,RMVar_hsa_circ_64835,RMVar_hsa_circ_6528,RMVar_hsa_circ_67831,RMVar_hsa_circ_353927,RMVar_hsa_circ_197045 21340 RMVar_ID_21340 Human_SNP_ID_60753274 A-to-I Human chr2 - 11336361 11336361 11336361 CTTGTGATCCTAGCTGCCCAGGAGGCTGAGGCAGGAGGATGGCTTGAGTCCAGGAGTTTGAGACT CTTGTGATCCTAGCTGCCCAGGAGGCTGAGGCGGGAGGATGGCTTGAGTCCAGGAGTTTGAGACT T C ROCK2 Ensembl:ENSG00000134318 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1323009274 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113994,RMVar_hsa_circ_197006 21341 RMVar_ID_21341 Human_SNP_ID_60860542 A-to-I Human chr2 + 11755851 11755851 11755851 TCAAGCGACTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGTGCGTGCCACTGTGCCTG TCAAGCGACTCTCCTGCCTCAGCCTCCTGAGTGGCTGGGACTACAGGTGCGTGCCACTGTGCCTG A G LPIN1 Ensembl:ENSG00000134324 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1023120182 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97283,RMVar_hsa_circ_197068 21342 RMVar_ID_21342 Human_SNP_ID_60874701 A-to-I Human chr2 + 11808753 11808753 11808753 AAAATTAGCCAGGGATGGTGGTGGGTGCCTGTAATCCCAGCTGCTCGGGAGGCTGAGGCAGAATT AAAATTAGCCAGGGATGGTGGTGGGTGCCTGTGATCCCAGCTGCTCGGGAGGCTGAGGCAGAATT A G LPIN1 Ensembl:ENSG00000134324 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs578071753 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 21343 RMVar_ID_21343 Human_SNP_ID_205724344 A-to-I Human chr4 + 139017462 139017462 139017462 GTTGGTCAGGCTGGCCTCGAACTCCCTAGCTCAGGTGAACCTCCCGCTTTGGCCTCCCAAAGTGC GTTGGTCAGGCTGGCCTCGAACTCCCTAGCTCGGGTGAACCTCCCGCTTTGGCCTCCCAAAGTGC A G NOCT Ensembl:ENSG00000151014 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1292491882 Functional Loss SNV dbSNP153 33..33 33 - - - 21344 RMVar_ID_21344 Human_SNP_ID_205724417 A-to-I Human chr4 + 139017620 139017620 139017620 GGGAGGCGGAGGCGGGTAGATCACCCGAGGTCAGGAGTTCGTGACCATCCTGGCCAATGGGCTTG GGGAGGCGGAGGCGGGTAGATCACCCGAGGTCGGGAGTTCGTGACCATCCTGGCCAATGGGCTTG A G NOCT Ensembl:ENSG00000151014 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs938376610 Functional Loss SNV dbSNP153 33..33 33 - - - 21345 RMVar_ID_21345 Human_SNP_ID_205724443 A-to-I Human chr4 + 139017737 139017737 139017737 GAATCACTTGAACCTGGGAGGCGGAGTGTTGCAGTGAGCCGAGATCGCACCATTGCACTCCAGCC GAATCACTTGAACCTGGGAGGCGGAGTGTTGCGGTGAGCCGAGATCGCACCATTGCACTCCAGCC A G NOCT Ensembl:ENSG00000151014 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs932200066 Functional Loss SNV dbSNP153 33..33 33 - - - 21346 RMVar_ID_21346 Human_SNP_ID_205724754 A-to-I Human chr4 + 139019195 139019195 139019195 CTCCTGTCTCAGCCTCCTGAGCAGCTGTGACTACAGGCACACGCCACTGTGCCGGGCTAATTTTT CTCCTGTCTCAGCCTCCTGAGCAGCTGTGACTGCAGGCACACGCCACTGTGCCGGGCTAATTTTT A G NOCT Ensembl:ENSG00000151014 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1325033458 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7270172 21347 RMVar_ID_21347 Human_SNP_ID_205731698 A-to-I Human chr4 + 139045616 139045616 139045616 TCGGCTCACTGCAAGATCCGCCTCCCGGGTTCATGGCATTCTCCTGCCTCAGCCTCCAGAGCAAC TCGGCTCACTGCAAGATCCGCCTCCCGGGTTCTTGGCATTCTCCTGCCTCAGCCTCCAGAGCAAC A T NOCT Ensembl:ENSG00000151014 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1181728678 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_228664,RMVar_hsa_circ_228665,RMVar_hsa_circ_228663 21348 RMVar_ID_21348 Human_SNP_ID_205732117 A-to-I Human chr4 + 139046776 139046776 139046776 TATTTTTAGTAGAGACGGGGTTTCACCATGTTAGTCAGGATGGTCTCAGTCTCGATCTCCTGACC TATTTTTAGTAGAGACGGGGTTTCACCATGTTGGTCAGGATGGTCTCAGTCTCGATCTCCTGACC A G - - Other Unknown GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1442723958 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_228664,RMVar_hsa_circ_228665,RMVar_hsa_circ_228663 21349 RMVar_ID_21349 Human_SNP_ID_205732276 A-to-I Human chr4 + 139047243 139047243 139047243 AACCTGGGTCGGGTGTGGTGGCTCATGCTTGTAATCCCAGCACTTTCGGAGGCCAAGGTGGGCGG AACCTGGGTCGGGTGTGGTGGCTCATGCTTGTGATCCCAGCACTTTCGGAGGCCAAGGTGGGCGG A G - - Other Unknown GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-Seq:(High) rs1265884660 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_228664,RMVar_hsa_circ_228665,RMVar_hsa_circ_228663 21350 RMVar_ID_21350 Human_SNP_ID_205732300 A-to-I Human chr4 + 139047299 139047299 139047299 GGTGGGCGGATCAACTGTGGTCAGGAGTTCGAAACCAGCCTGGCCAACATGGTGAAACCTCGTCT GGTGGGCGGATCAACTGTGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCTCGTCT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355641438 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_228664,RMVar_hsa_circ_228665,RMVar_hsa_circ_228663 21351 RMVar_ID_21351 Human_SNP_ID_205732334 A-to-I Human chr4 + 139047388 139047388 139047388 GGGCATGGTGGCAGGTGTCTGTAATCCCAGCTACTTGGGAGGCTGAAACAGGAGAATCGCTTGAA GGGCATGGTGGCAGGTGTCTGTAATCCCAGCTGCTTGGGAGGCTGAAACAGGAGAATCGCTTGAA A G - - Other Unknown GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs904963131 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_228664,RMVar_hsa_circ_228665,RMVar_hsa_circ_228663 21352 RMVar_ID_21352 Human_SNP_ID_205732369 A-to-I Human chr4 + 139047488 139047488 139047488 ACCATTGCGCTCTAGCCTGGGCAACAAGAGTGAAACTCCATCTCAAAAAAACCTGGAATTCTCTT ACCATTGCGCTCTAGCCTGGGCAACAAGAGTGCAACTCCATCTCAAAAAAACCTGGAATTCTCTT A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985919149 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8126609,Human_RBP_ID_27510038 RMVar_hsa_circ_228664,RMVar_hsa_circ_228665,RMVar_hsa_circ_228663 21353 RMVar_ID_21353 Human_SNP_ID_205733738 A-to-I Human chr4 - 139051899 139051899 139051899 GGAATGTAGTGGCACGATCTCAGCTCACTGCAACCTGTGCCTCCCAGGTTCAAGCAATAATACTC GGAATGTAGTGGCACGATCTCAGCTCACTGCATCCTGTGCCTCCCAGGTTCAAGCAATAATACTC T A ELF2 Ensembl:ENSG00000109381 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1188108538 Functional Loss SNV dbSNP153 33..33 33 - - - 21354 RMVar_ID_21354 Human_SNP_ID_205733740 A-to-I Human chr4 - 139051905 139051905 139051905 CAGGCTGGAATGTAGTGGCACGATCTCAGCTCACTGCAACCTGTGCCTCCCAGGTTCAAGCAATA CAGGCTGGAATGTAGTGGCACGATCTCAGCTCCCTGCAACCTGTGCCTCCCAGGTTCAAGCAATA T G ELF2 Ensembl:ENSG00000109381 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1359988782 Functional Loss SNV dbSNP153 33..33 33 - - - 21355 RMVar_ID_21355 Human_SNP_ID_205733745 A-to-I Human chr4 - 139051928 139051928 139051928 GGAGACAGTCTAGCTCTGTCATCCAGGCTGGAATGTAGTGGCACGATCTCAGCTCACTGCAACCT GGAGACAGTCTAGCTCTGTCATCCAGGCTGGAGTGTAGTGGCACGATCTCAGCTCACTGCAACCT T C ELF2 Ensembl:ENSG00000109381 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1343918449 Functional Loss SNV dbSNP153 33..33 33 - - - 21356 RMVar_ID_21356 Human_SNP_ID_205734031 A-to-I Human chr4 - 139053231 139053231 139053231 TCTCAGGTGATCCACCTGCCTCAGCTTCCCAAAGTGCTGGCATTATAGGCGTGAGCCATCACACC TCTCAGGTGATCCACCTGCCTCAGCTTCCCAAGGTGCTGGCATTATAGGCGTGAGCCATCACACC T C ELF2 Ensembl:ENSG00000109381 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1269356793 Functional Loss SNV dbSNP153 33..33 33 - - - 21357 RMVar_ID_21357 Human_SNP_ID_205734032 A-to-I Human chr4 - 139053231 139053231 139053231 TCTCAGGTGATCCACCTGCCTCAGCTTCCCAAAGTGCTGGCATTATAGGCGTGAGCCATCACACC TCTCAGGTGATCCACCTGCCTCAGCTTCCCAACGTGCTGGCATTATAGGCGTGAGCCATCACACC T G ELF2 Ensembl:ENSG00000109381 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1269356793 Functional Loss SNV dbSNP153 33..33 33 - - - 21358 RMVar_ID_21358 Human_SNP_ID_205734102 A-to-I Human chr4 - 139053473 139053473 139053473 TCCATTGCACTGTAGAATCTTTATTTTTTGAGACAGAGTCTCTCTCTGTCACCCAGGCTGGAGTG TCCATTGCACTGTAGAATCTTTATTTTTTGAGGCAGAGTCTCTCTCTGTCACCCAGGCTGGAGTG T C ELF2 Ensembl:ENSG00000109381 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1418090374 Functional Loss SNV dbSNP153 33..33 33 - - - 21359 RMVar_ID_21359 Human_SNP_ID_205734189 A-to-I Human chr4 - 139053798 139053798 139053798 CCTGGCTAACACAGTGAAAGCCCATCTCTACTAAAAATACAAAAAATTAGCAGGGTGTGGTGGCG CCTGGCTAACACAGTGAAAGCCCATCTCTACTGAAAATACAAAAAATTAGCAGGGTGTGGTGGCG T C ELF2 Ensembl:ENSG00000109381 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1184638115 Functional Loss SNV dbSNP153 33..33 33 - - - 21360 RMVar_ID_21360 Human_SNP_ID_205734698 A-to-I Human chr4 + 139056144 139056144 139056144 GGAGTAACTAAATCATCTGTAACAAGGGGTCCAGGAATGGAGAGAATTCACAGCTCATGACCATG GGAGTAACTAAATCATCTGTAACAAGGGGTCCGGGAATGGAGAGAATTCACAGCTCATGACCATG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1176118152 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_228663 21361 RMVar_ID_21361 Human_SNP_ID_205744930 A-to-I Human chr4 - 139096103 139096103 139096103 CTACAAATGTTCTTTTTTTGTATGTATGACAGAGTCTTGTTCTGTTGCCCAGGCTGGAGTGCAGT CTACAAATGTTCTTTTTTTGTATGTATGACAGGGTCTTGTTCTGTTGCCCAGGCTGGAGTGCAGT T C ELF2 Ensembl:ENSG00000109381 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1254566673 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_160277 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 21362 RMVar_ID_21362 Human_SNP_ID_205763620 A-to-I Human chr4 - 139170922 139170922 139170922 GGTCAGCATGGTAAAACCCTGTCTCTACTAAAAATACAAAAATTAGCCGGAGGTGGTGGCGCATG GGTCAGCATGGTAAAACCCTGTCTCTACTAAATATACAAAAATTAGCCGGAGGTGGTGGCGCATG T A ELF2 Ensembl:ENSG00000109381 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1415122999 Functional Loss SNV dbSNP153 33..33 33 - - - 21363 RMVar_ID_21363 Human_SNP_ID_205763641 A-to-I Human chr4 - 139171027 139171027 139171027 AATTGGGTTGTTTGGGCTGGGTGCGGTGGCTCATGCCTGTAACCCCAGCACTTTGGGAGGCTGAG AATTGGGTTGTTTGGGCTGGGTGCGGTGGCTCGTGCCTGTAACCCCAGCACTTTGGGAGGCTGAG T C ELF2 Ensembl:ENSG00000109381 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1271228989 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17574861,Human_RBP_ID_22611852 21364 RMVar_ID_21364 Human_SNP_ID_205793685 A-to-I Human chr4 - 139292269 139292269 139292269 CTGTTGGCCAGGCTGGTCTCACTCCTTGCCTCAGCTTCTGAAAATGTTGGAATTATAGGTATGAG CTGTTGGCCAGGCTGGTCTCACTCCTTGCCTCGGCTTCTGAAAATGTTGGAATTATAGGTATGAG T C NDUFC1 Ensembl:ENSG00000109390 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1284878373 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_228692 21365 RMVar_ID_21365 Human_SNP_ID_205795226 A-to-I Human chr4 - 139297987 139297987 139297987 TTGGCTTACTGTAGCCTCACCTCCCAGGTCCAAGCGATCTTCCAACCTCAGCCTCCCGAGTAGCT TTGGCTTACTGTAGCCTCACCTCCCAGGTCCAGGCGATCTTCCAACCTCAGCCTCCCGAGTAGCT T C NDUFC1 Ensembl:ENSG00000109390 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs533491335 Functional Loss SNV dbSNP153 33..33 33 - - - 21366 RMVar_ID_21366 Human_SNP_ID_205798076 A-to-I Human chr4 + 139308709 139308709 139308709 CACTCTCCGACTCACTGCAACCTCCACCTCCCAGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCC CACTCTCCGACTCACTGCAACCTCCACCTCCCCGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCC A C NAA15 Ensembl:ENSG00000164134 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1358624308 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268801 21367 RMVar_ID_21367 Human_SNP_ID_205798212 A-to-I Human chr4 + 139309227 139309227 139309227 AAACTTAGCTGGGCGTGGTTGCAGGCACCTGTAATCCCAGCTACTTGGGAGGCTGAGGCGGGAGA AAACTTAGCTGGGCGTGGTTGCAGGCACCTGTTATCCCAGCTACTTGGGAGGCTGAGGCGGGAGA A T NAA15 Ensembl:ENSG00000164134 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1396249863 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268801 21368 RMVar_ID_21368 Human_SNP_ID_205798717 A-to-I Human chr4 + 139310940 139310939 139310941 TATGCCTGGCCTAATTTAAAAAATTTTGAGACAGAGTCTTACTCTGTTGCCCAGGCTGGAGGGCT TATGCCTGGCCTAATTTAAAAAATTTTGAGAC__AGTCTTACTCTGTTGCCCAGGCTGGAGGGCT CAG C NAA15 Ensembl:ENSG00000164134 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1364656501 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_15055271 RMVar_hsa_circ_268801 21369 RMVar_ID_21369 Human_SNP_ID_205799629 A-to-I Human chr4 + 139314817 139314816 139314817 CTCCTGCCTCAGCCTCCTGAATAGCTGGGATTACAGGCGTGTGCCACCATGCCCAGCAAATTTTT CTCCTGCCTCAGCCTCCTGAATAGCTGGGATT_CAGGCGTGTGCCACCATGCCCAGCAAATTTTT TA T NAA15 Ensembl:ENSG00000164134 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1162351670 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_268801 21370 RMVar_ID_21370 Human_SNP_ID_205805903 A-to-I Human chr4 + 139338613 139338613 139338613 GGCATTACAGGTGCACAGCACCAAGCCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCA GGCATTACAGGTGCACAGCACCAAGCCTGGCTGATTTTTGTATTTTTAGTAGAGACAGGGTTTCA A G NAA15 Ensembl:ENSG00000164134 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs991438019 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5434,RMVar_hsa_circ_228693,RMVar_hsa_circ_327149,RMVar_hsa_circ_268801,RMVar_hsa_circ_348772,RMVar_hsa_circ_362426,RMVar_hsa_circ_347425,RMVar_hsa_circ_74193,RMVar_hsa_circ_121784,RMVar_hsa_circ_228694,RMVar_hsa_circ_228695,RMVar_hsa_circ_44100,RMVar_hsa_circ_270742,RMVar_hsa_circ_335975,RMVar_hsa_circ_361962,RMVar_hsa_circ_287789,RMVar_hsa_circ_58515,RMVar_hsa_circ_22637,RMVar_hsa_circ_228697,RMVar_hsa_circ_228698,RMVar_hsa_circ_228696 21371 RMVar_ID_21371 Human_SNP_ID_205806044 A-to-I Human chr4 + 139339239 139339239 139339239 TTATTTTGGGCCAGCCACAGTGACTCATGCCCATAATCCCAGCACTTTGGGAGGCTGAGGCAGCG TTATTTTGGGCCAGCCACAGTGACTCATGCCCGTAATCCCAGCACTTTGGGAGGCTGAGGCAGCG A G NAA15 Ensembl:ENSG00000164134 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs901380010 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17575170 RMVar_hsa_circ_5434,RMVar_hsa_circ_228693,RMVar_hsa_circ_327149,RMVar_hsa_circ_268801,RMVar_hsa_circ_348772,RMVar_hsa_circ_362426,RMVar_hsa_circ_347425,RMVar_hsa_circ_74193,RMVar_hsa_circ_121784,RMVar_hsa_circ_228694,RMVar_hsa_circ_228695,RMVar_hsa_circ_44100,RMVar_hsa_circ_270742,RMVar_hsa_circ_335975,RMVar_hsa_circ_361962,RMVar_hsa_circ_287789,RMVar_hsa_circ_58515,RMVar_hsa_circ_22637,RMVar_hsa_circ_228697,RMVar_hsa_circ_228698,RMVar_hsa_circ_228696 21372 RMVar_ID_21372 Human_SNP_ID_205808831 A-to-I Human chr4 + 139350233 139350233 139350233 GGGAGGCTGGGGCGGGAGGATTGCTTGAGCCCAGGAGTTTGAGCTCAGCATGGGCAACATGGTGA GGGAGGCTGGGGCGGGAGGATTGCTTGAGCCCCGGAGTTTGAGCTCAGCATGGGCAACATGGTGA A C NAA15 Ensembl:ENSG00000164134 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1257651665 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1102,RMVar_hsa_circ_268801,RMVar_hsa_circ_348772,RMVar_hsa_circ_74193,RMVar_hsa_circ_121784,RMVar_hsa_circ_228694,RMVar_hsa_circ_228695,RMVar_hsa_circ_44100,RMVar_hsa_circ_335975,RMVar_hsa_circ_361962,RMVar_hsa_circ_58515,RMVar_hsa_circ_22637,RMVar_hsa_circ_66034,RMVar_hsa_circ_228696,RMVar_hsa_circ_31343,RMVar_hsa_circ_56849,RMVar_hsa_circ_8998,RMVar_hsa_circ_40043,RMVar_hsa_circ_68814,RMVar_hsa_circ_312320,RMVar_hsa_circ_44232,RMVar_hsa_circ_228701 21373 RMVar_ID_21373 Human_SNP_ID_205811035 A-to-I Human chr4 + 139359311 139359311 139359311 CCACCACCCTTGGTTTACTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAAGTTTG CCACCACCCTTGGTTTACTTTGTATTTTTAGTGGAGATGGGGTTTCACCATGTTGGCCAAGTTTG A G NAA15 Ensembl:ENSG00000164134 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs138813037 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1102,RMVar_hsa_circ_348772,RMVar_hsa_circ_121784,RMVar_hsa_circ_228694,RMVar_hsa_circ_228695,RMVar_hsa_circ_44100,RMVar_hsa_circ_22637,RMVar_hsa_circ_228696,RMVar_hsa_circ_31343,RMVar_hsa_circ_39319,RMVar_hsa_circ_40043,RMVar_hsa_circ_68814,RMVar_hsa_circ_51640,RMVar_hsa_circ_376577,RMVar_hsa_circ_27237,RMVar_hsa_circ_84666,RMVar_hsa_circ_228704,RMVar_hsa_circ_47232 21374 RMVar_ID_21374 Human_SNP_ID_205813805 A-to-I Human chr4 + 139371380 139371355 139371381 AGGAGGCTGAGGTGGGAGGATCACTTGAATCTAGGAGTTCAAGGCTGCAGTACACTGTGAGCTAT AGGAGGCT__________________________GAGTTCAAGGCTGCAGTACACTGTGAGCTAT TGAGGTGGGAGGATCACTTGAATCTAG T NAA15 Ensembl:ENSG00000164134 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1460858869 Functional Loss DEL dbSNP153 9..34 33 - - - Human_RBP_ID_15056960 RMVar_hsa_circ_121784,RMVar_hsa_circ_228695,RMVar_hsa_circ_22637,RMVar_hsa_circ_31343,RMVar_hsa_circ_39319,RMVar_hsa_circ_376577,RMVar_hsa_circ_45370,RMVar_hsa_circ_228706,RMVar_hsa_circ_77949,RMVar_hsa_circ_228707,RMVar_hsa_circ_311357,RMVar_hsa_circ_350026,RMVar_hsa_circ_355480,RMVar_hsa_circ_228708 21375 RMVar_ID_21375 Human_SNP_ID_205813809 A-to-I Human chr4 + 139371380 139371380 139371380 AGGAGGCTGAGGTGGGAGGATCACTTGAATCTAGGAGTTCAAGGCTGCAGTACACTGTGAGCTAT AGGAGGCTGAGGTGGGAGGATCACTTGAATCTGGGAGTTCAAGGCTGCAGTACACTGTGAGCTAT A G NAA15 Ensembl:ENSG00000164134 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1258100721 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15056960 RMVar_hsa_circ_121784,RMVar_hsa_circ_228695,RMVar_hsa_circ_22637,RMVar_hsa_circ_31343,RMVar_hsa_circ_39319,RMVar_hsa_circ_376577,RMVar_hsa_circ_45370,RMVar_hsa_circ_228706,RMVar_hsa_circ_77949,RMVar_hsa_circ_228707,RMVar_hsa_circ_311357,RMVar_hsa_circ_350026,RMVar_hsa_circ_355480,RMVar_hsa_circ_228708 21376 RMVar_ID_21376 Human_SNP_ID_205855797 A-to-I Human chr4 - 139550171 139550171 139550171 TCTTCATTTGCCTGTTGAAAGGCACTGAGGCCAGGTGTGGTGGTTCTTGCCTGTAATCCCAGCAC TCTTCATTTGCCTGTTGAAAGGCACTGAGGCCGGGTGTGGTGGTTCTTGCCTGTAATCCCAGCAC T C SETD7 Ensembl:ENSG00000145391 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1422417358 Functional Loss SNV dbSNP153 33..33 33 - - - 21377 RMVar_ID_21377 Human_SNP_ID_205867755 A-to-I Human chr4 - 139599481 139599479 139599482 TAGGTTTTATTATTATTATTAGTAGTAGTAGTAGAGACAGCGTTTCACCATGTTGGCCAGGCTGG TAGGTTTTATTATTATTATTAGTAGTAGTAG___AGACAGCGTTTCACCATGTTGGCCAGGCTGG TCTA T SETD7 Ensembl:ENSG00000145391 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs780086990 Functional Loss DEL dbSNP153 32..34 33 - - - 21378 RMVar_ID_21378 Human_SNP_ID_205867798 A-to-I Human chr4 - 139599596 139599596 139599596 GGAGTGCAGTGGCACAATCTCGGCTCACTGCAACTTCTGCCTCCTGGGTTCCAGTGATTCTTCTG GGAGTGCAGTGGCACAATCTCGGCTCACTGCAGCTTCTGCCTCCTGGGTTCCAGTGATTCTTCTG T C SETD7 Ensembl:ENSG00000145391 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs529108927 Functional Loss SNV dbSNP153 33..33 33 - - - 21379 RMVar_ID_21379 Human_SNP_ID_205867799 A-to-I Human chr4 - 139599596 139599596 139599596 GGAGTGCAGTGGCACAATCTCGGCTCACTGCAACTTCTGCCTCCTGGGTTCCAGTGATTCTTCTG GGAGTGCAGTGGCACAATCTCGGCTCACTGCACCTTCTGCCTCCTGGGTTCCAGTGATTCTTCTG T G SETD7 Ensembl:ENSG00000145391 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs529108927 Functional Loss SNV dbSNP153 33..33 33 - - - 21380 RMVar_ID_21380 Human_SNP_ID_205897737 A-to-I Human chr4 + 139723212 139723212 139723212 CAGCTTCAAAAACCCATGTACAGTACAATCCCAATTTTTGTGGGTGTCTATTTATATAGAAACAA CAGCTTCAAAAACCCATGTACAGTACAATCCCGATTTTTGTGGGTGTCTATTTATATAGAAACAA A G MGST2 Ensembl:ENSG00000085871 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749353338 Functional Loss SNV dbSNP153 33..33 33 - - - 21381 RMVar_ID_21381 Human_SNP_ID_205985094 A-to-I Human chr4 - 140104141 140104141 140104141 GGCTCAAGTGATCCTCCCACCTTGGCCTCCCAAAGTGCTGGATTACAGGCATGAGCCACTACATT GGCTCAAGTGATCCTCCCACCTTGGCCTCCCACAGTGCTGGATTACAGGCATGAGCCACTACATT T G MAML3 Ensembl:ENSG00000196782 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs904900975 Functional Loss SNV dbSNP153 33..33 33 - - - 21382 RMVar_ID_21382 Human_SNP_ID_206226061 A-to-I Human chr4 - 141106742 141106742 141106742 TCACCCACACTGGAGTGCAATGGCACGATGTCAGCTCACTGCAATTTCCGCCTCCCGGGTTCAAG TCACCCACACTGGAGTGCAATGGCACGATGTCGGCTCACTGCAATTTCCGCCTCCCGGGTTCAAG T C RNF150 Ensembl:ENSG00000170153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1467117142 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_228759 21383 RMVar_ID_21383 Human_SNP_ID_206361974 A-to-I Human chr4 + 141666903 141666903 141666903 TGCTGGGTTGCCCCACTCAGCCTATTCATATTAGGTCATACTCTCTTTGTCCAGTCATATTTTTA TGCTGGGTTGCCCCACTCAGCCTATTCATATTGGGTCATACTCTCTTTGTCCAGTCATATTTTTA A G IL15 Ensembl:ENSG00000164136 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903328667 Functional Loss SNV dbSNP153 33..33 33 - - - 21384 RMVar_ID_21384 Human_SNP_ID_206362478 A-to-I Human chr4 + 141669092 141669092 141669092 ATCATTTTATGATGATAATTTAAATGTCATTTAAAATGATGACAAAATAGTCCCTTTCTTAAAAA ATCATTTTATGATGATAATTTAAATGTCATTTTAAATGATGACAAAATAGTCCCTTTCTTAAAAA A T IL15 Ensembl:ENSG00000164136 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1024087900 Functional Loss SNV dbSNP153 33..33 33 - - - 21385 RMVar_ID_21385 Human_SNP_ID_206794269 A-to-I Human chr4 + 143416694 143416694 143416694 TACCCAGGAGGCTGAGGCAGGAGAATCGCTTGAACCCAGGAGGCGGAGGCTACAGTGAGCCACAA TACCCAGGAGGCTGAGGCAGGAGAATCGCTTGTACCCAGGAGGCGGAGGCTACAGTGAGCCACAA A T GAB1 Ensembl:ENSG00000109458 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs774390810 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_917,RMVar_hsa_circ_336923,RMVar_hsa_circ_360100,RMVar_hsa_circ_337891,RMVar_hsa_circ_307499,RMVar_hsa_circ_267101,RMVar_hsa_circ_293470,RMVar_hsa_circ_73258,RMVar_hsa_circ_228799,RMVar_hsa_circ_228798 21386 RMVar_ID_21386 Human_SNP_ID_206908262 A-to-I Human chr4 + 143875834 143875834 143875834 CTGCTATTAAAAAAATACAAAAATTAGTCAGGAATGGTGGCCCGCACCTGTAGTCCCAACTACTG CTGCTATTAAAAAAATACAAAAATTAGTCAGGCATGGTGGCCCGCACCTGTAGTCCCAACTACTG A C AC107223.1 Ensembl:ENSG00000251600 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs80063093 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_228821,RMVar_hsa_circ_336685 21387 RMVar_ID_21387 Human_SNP_ID_207202094 A-to-I Human chr4 - 145037762 145037762 145037762 TTGTGTTTTTTGTAGAGACAGGGTTTTGCCATATTGGCCAGGCTGCTCTGAAACTCCTGGGCTCC TTGTGTTTTTTGTAGAGACAGGGTTTTGCCATGTTGGCCAGGCTGCTCTGAAACTCCTGGGCTCC T C ANAPC10,AC098588.2 Ensembl:ENSG00000164162,Ensembl:ENSG00000285713 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs770493120 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102970,RMVar_hsa_circ_228831 21388 RMVar_ID_21388 Human_SNP_ID_207205996 A-to-I Human chr4 - 145054177 145054177 145054177 TCAGGCTGGGCACGGTGGCTCAGGCCTGTAATACCAGCACTTTGGGAGGCCGCAGCGGGCAGATC TCAGGCTGGGCACGGTGGCTCAGGCCTGTAATGCCAGCACTTTGGGAGGCCGCAGCGGGCAGATC T C ANAPC10,AC098588.2 Ensembl:ENSG00000164162,Ensembl:ENSG00000285713 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs963861197 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17574870 RMVar_hsa_circ_228832,RMVar_hsa_circ_102970,RMVar_hsa_circ_228831 21389 RMVar_ID_21389 Human_SNP_ID_207205997 A-to-I Human chr4 - 145054177 145054177 145054177 TCAGGCTGGGCACGGTGGCTCAGGCCTGTAATACCAGCACTTTGGGAGGCCGCAGCGGGCAGATC TCAGGCTGGGCACGGTGGCTCAGGCCTGTAATCCCAGCACTTTGGGAGGCCGCAGCGGGCAGATC T G ANAPC10,AC098588.2 Ensembl:ENSG00000164162,Ensembl:ENSG00000285713 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs963861197 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17574870 RMVar_hsa_circ_228832,RMVar_hsa_circ_102970,RMVar_hsa_circ_228831 21390 RMVar_ID_21390 Human_SNP_ID_207205999 A-to-I Human chr4 - 145054179 145054179 145054179 AATCAGGCTGGGCACGGTGGCTCAGGCCTGTAATACCAGCACTTTGGGAGGCCGCAGCGGGCAGA AATCAGGCTGGGCACGGTGGCTCAGGCCTGTAGTACCAGCACTTTGGGAGGCCGCAGCGGGCAGA T C ANAPC10,AC098588.2 Ensembl:ENSG00000164162,Ensembl:ENSG00000285713 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs763373469 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17574870 RMVar_hsa_circ_228832,RMVar_hsa_circ_102970,RMVar_hsa_circ_228831 21391 RMVar_ID_21391 Human_SNP_ID_207223302 A-to-I Human chr4 + 145126511 145126511 145126511 TAGAGATGGGGTTTCACCATCTTGCCCGTGCTAGTCTTGAACTCCTGACCTAGTGTTCCACCTGC TAGAGATGGGGTTTCACCATCTTGCCCGTGCTGGTCTTGAACTCCTGACCTAGTGTTCCACCTGC A G ABCE1 Ensembl:ENSG00000164163 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs536542162 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15064310 21392 RMVar_ID_21392 Human_SNP_ID_207231203 A-to-I Human chr4 - 145156467 145156467 145156467 GTTGGTCAGGCTGGTCTTGAACTCTCAAACTCAGGTGATCTGCCTGCCTGTGCCTCCCAAAGTCC GTTGGTCAGGCTGGTCTTGAACTCTCAAACTCGGGTGATCTGCCTGCCTGTGCCTCCCAAAGTCC T C OTUD4 Ensembl:ENSG00000164164 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1237994336 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2822871,Human_RBP_ID_15065178 RMVar_hsa_circ_117385,RMVar_hsa_circ_228843,RMVar_hsa_circ_228845,RMVar_hsa_circ_126845,RMVar_hsa_circ_34565,RMVar_hsa_circ_292116,RMVar_hsa_circ_59380,RMVar_hsa_circ_358305,RMVar_hsa_circ_63789,RMVar_hsa_circ_300182,RMVar_hsa_circ_41862,RMVar_hsa_circ_228850,RMVar_hsa_circ_7164 21393 RMVar_ID_21393 Human_SNP_ID_207235110 A-to-I Human chr4 - 145171319 145171319 145171319 GGTGAAGTTTGATTTCTTTTTTTTTTTTTTTGAGGTGGAATTTAACTCCATTGCCAGGCTGGAGT GGTGAAGTTTGATTTCTTTTTTTTTTTTTTTGTGGTGGAATTTAACTCCATTGCCAGGCTGGAGT T A OTUD4 Ensembl:ENSG00000164164 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs953042093 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15065553 RMVar_hsa_circ_228845,RMVar_hsa_circ_126845,RMVar_hsa_circ_292116,RMVar_hsa_circ_358305,RMVar_hsa_circ_300182,RMVar_hsa_circ_41862,RMVar_hsa_circ_228850,RMVar_hsa_circ_293831,RMVar_hsa_circ_228852,RMVar_hsa_circ_290027,RMVar_hsa_circ_370159,RMVar_hsa_circ_228851,RMVar_hsa_circ_228853,RMVar_hsa_circ_228854,RMVar_hsa_circ_284686 21394 RMVar_ID_21394 Human_SNP_ID_207235111 A-to-I Human chr4 - 145171319 145171319 145171319 GGTGAAGTTTGATTTCTTTTTTTTTTTTTTTGAGGTGGAATTTAACTCCATTGCCAGGCTGGAGT GGTGAAGTTTGATTTCTTTTTTTTTTTTTTTGGGGTGGAATTTAACTCCATTGCCAGGCTGGAGT T C OTUD4 Ensembl:ENSG00000164164 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs953042093 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15065553 RMVar_hsa_circ_228845,RMVar_hsa_circ_126845,RMVar_hsa_circ_292116,RMVar_hsa_circ_358305,RMVar_hsa_circ_300182,RMVar_hsa_circ_41862,RMVar_hsa_circ_228850,RMVar_hsa_circ_293831,RMVar_hsa_circ_228852,RMVar_hsa_circ_290027,RMVar_hsa_circ_370159,RMVar_hsa_circ_228851,RMVar_hsa_circ_228853,RMVar_hsa_circ_228854,RMVar_hsa_circ_284686 21395 RMVar_ID_21395 Human_SNP_ID_207326004 A-to-I Human chr4 + 145544506 145544506 145544506 GGGAGGCTGAGGCAGGAGAATCACTTGAACCCAGGAGGCAGAGGTTGCAGTGAACTGAGATCACA GGGAGGCTGAGGCAGGAGAATCACTTGAACCCCGGAGGCAGAGGTTGCAGTGAACTGAGATCACA A C SMAD1 Ensembl:ENSG00000170365 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1188166675 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81302,RMVar_hsa_circ_110653,RMVar_hsa_circ_228859,RMVar_hsa_circ_228860 21396 RMVar_ID_21396 Human_SNP_ID_207553243 A-to-I Human chr4 - 146492588 146492588 146492588 AGGCCAGTGGATCACGAGCTTAGGAGTTTCAGACCTGCCTGGGTGACATGGCAAAACCCCATCTT AGGCCAGTGGATCACGAGCTTAGGAGTTTCAGCCCTGCCTGGGTGACATGGCAAAACCCCATCTT T G SLC10A7 Ensembl:ENSG00000120519 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1310846036 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_294244,RMVar_hsa_circ_342165,RMVar_hsa_circ_228899 21397 RMVar_ID_21397 Human_SNP_ID_207825263 A-to-I Human chr4 + 147634910 147634909 147634911 CACCATGCCCAGCTAATTTTTTTTTTTTCAGTAGAGACAGGGTCTCACCATGTTAGCCAGGATGG CACCATGCCCAGCTAATTTTTTTTTTTTCAGT__AGACAGGGTCTCACCATGTTAGCCAGGATGG TAG T TMEM184C Ensembl:ENSG00000164168 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1022628003 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_2823240 RMVar_hsa_circ_266620 21398 RMVar_ID_21398 Human_SNP_ID_207825286 A-to-I Human chr4 + 147634983 147634983 147634983 TGACCTCGTGATCCGCCGACCTCGGCCTCCCAAAGTGCTGGAATTACAGGCGTGAGCCACTGCGC TGACCTCGTGATCCGCCGACCTCGGCCTCCCAGAGTGCTGGAATTACAGGCGTGAGCCACTGCGC A G TMEM184C Ensembl:ENSG00000164168 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs374669898 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_163120 RMVar_hsa_circ_266620 21399 RMVar_ID_21399 Human_SNP_ID_207832145 A-to-I Human chr4 - 147663490 147663490 147663490 GTGGTGGCATGCACCTGTAGTCCCAGCTACTCAGGAAGTGGAGATAGGAGAATTGCTTGAGCCTG GTGGTGGCATGCACCTGTAGTCCCAGCTACTCCGGAAGTGGAGATAGGAGAATTGCTTGAGCCTG T G PRMT9 Ensembl:ENSG00000164169 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1043716649 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_376452,RMVar_hsa_circ_337888,RMVar_hsa_circ_64218,RMVar_hsa_circ_310267,RMVar_hsa_circ_355977 21400 RMVar_ID_21400 Human_SNP_ID_207832169 A-to-I Human chr4 - 147663593 147663593 147663593 GGGAGGCAAAGGTGGGCAGATGGCCTGAGCTCAGGAGTTTGAGAGCAGCCTGGGCAACACAGCGA GGGAGGCAAAGGTGGGCAGATGGCCTGAGCTCGGGAGTTTGAGAGCAGCCTGGGCAACACAGCGA T C PRMT9 Ensembl:ENSG00000164169 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1447360091 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11954 RMVar_hsa_circ_376452,RMVar_hsa_circ_337888,RMVar_hsa_circ_64218,RMVar_hsa_circ_310267,RMVar_hsa_circ_355977 21401 RMVar_ID_21401 Human_SNP_ID_207855921 A-to-I Human chr4 + 147757294 147757294 147757294 TGGGCTCACTGCAACCTCTGCCTCCCGTGTTCAAGCAATTCCCCTGCCTCAGCCTCCCGAAAGCT TGGGCTCACTGCAACCTCTGCCTCCCGTGTTCGAGCAATTCCCCTGCCTCAGCCTCCCGAAAGCT A G ARHGAP10 Ensembl:ENSG00000071205 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1055929198 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_228915,RMVar_hsa_circ_79750 21402 RMVar_ID_21402 Human_SNP_ID_207855935 A-to-I Human chr4 + 147757333 147757333 147757333 TCCCCTGCCTCAGCCTCCCGAAAGCTGGGACTACAGGCGTATGCCGCCATGCCCAGCTAATTTCT TCCCCTGCCTCAGCCTCCCGAAAGCTGGGACTGCAGGCGTATGCCGCCATGCCCAGCTAATTTCT A G ARHGAP10 Ensembl:ENSG00000071205 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1292944521 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_228915,RMVar_hsa_circ_79750 21403 RMVar_ID_21403 Human_SNP_ID_207889575 A-to-I Human chr4 + 147886991 147886990 147886992 GAGTTTCAGTTTCACCTTGAACTCCTGAACTCAAGAGATCCACCTGCCTCGGCCTCCCAAAGTGC GAGTTTCAGTTTCACCTTGAACTCCTGAACTC__GAGATCCACCTGCCTCGGCCTCCCAAAGTGC CAA C ARHGAP10 Ensembl:ENSG00000071205 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1272162759 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_37033,RMVar_hsa_circ_100243,RMVar_hsa_circ_347626,RMVar_hsa_circ_121902,RMVar_hsa_circ_228917,RMVar_hsa_circ_228916,RMVar_hsa_circ_228924,RMVar_hsa_circ_72206,RMVar_hsa_circ_228923,RMVar_hsa_circ_103665,RMVar_hsa_circ_33616,RMVar_hsa_circ_349672,RMVar_hsa_circ_354540,RMVar_hsa_circ_351827,RMVar_hsa_circ_347286,RMVar_hsa_circ_287448,RMVar_hsa_circ_228929,RMVar_hsa_circ_46775,RMVar_hsa_circ_228928,RMVar_hsa_circ_347126,RMVar_hsa_circ_376986,RMVar_hsa_circ_106561,RMVar_hsa_circ_267340,RMVar_hsa_circ_79527,RMVar_hsa_circ_50447,RMVar_hsa_circ_228931,RMVar_hsa_circ_228932,RMVar_hsa_circ_95410,RMVar_hsa_circ_127839,RMVar_hsa_circ_228933,RMVar_hsa_circ_228934,RMVar_hsa_circ_49876 21404 RMVar_ID_21404 Human_SNP_ID_207889767 A-to-I Human chr4 + 147887715 147887715 147887715 TAAACCCCATCTCTACTAAAAATACAAAAATTAGCCGGGTGTGGTGGCGGGCGCTTGTAGTCCCA TAAACCCCATCTCTACTAAAAATACAAAAATTTGCCGGGTGTGGTGGCGGGCGCTTGTAGTCCCA A T ARHGAP10 Ensembl:ENSG00000071205 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1249418609 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37033,RMVar_hsa_circ_100243,RMVar_hsa_circ_347626,RMVar_hsa_circ_121902,RMVar_hsa_circ_228917,RMVar_hsa_circ_228916,RMVar_hsa_circ_228924,RMVar_hsa_circ_72206,RMVar_hsa_circ_228923,RMVar_hsa_circ_103665,RMVar_hsa_circ_33616,RMVar_hsa_circ_349672,RMVar_hsa_circ_354540,RMVar_hsa_circ_351827,RMVar_hsa_circ_347286,RMVar_hsa_circ_287448,RMVar_hsa_circ_228929,RMVar_hsa_circ_46775,RMVar_hsa_circ_228928,RMVar_hsa_circ_347126,RMVar_hsa_circ_376986,RMVar_hsa_circ_106561,RMVar_hsa_circ_267340,RMVar_hsa_circ_79527,RMVar_hsa_circ_50447,RMVar_hsa_circ_228931,RMVar_hsa_circ_228932,RMVar_hsa_circ_95410,RMVar_hsa_circ_127839,RMVar_hsa_circ_228933,RMVar_hsa_circ_228934,RMVar_hsa_circ_49876 21405 RMVar_ID_21405 Human_SNP_ID_207889778 A-to-I Human chr4 + 147887741 147887736 147887742 AAAATTAGCCGGGTGTGGTGGCGGGCGCTTGTAGTCCCAGCTACTCAGGAGGCTGAGACAGGAGA AAAATTAGCCGGGTGTGGTGGCGGGCGC______TCCCAGCTACTCAGGAGGCTGAGACAGGAGA CTTGTAG C ARHGAP10 Ensembl:ENSG00000071205 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170336692 Functional Loss DEL dbSNP153 29..34 33 - - - RMVar_hsa_circ_37033,RMVar_hsa_circ_100243,RMVar_hsa_circ_347626,RMVar_hsa_circ_121902,RMVar_hsa_circ_228917,RMVar_hsa_circ_228916,RMVar_hsa_circ_228924,RMVar_hsa_circ_72206,RMVar_hsa_circ_228923,RMVar_hsa_circ_103665,RMVar_hsa_circ_33616,RMVar_hsa_circ_349672,RMVar_hsa_circ_354540,RMVar_hsa_circ_351827,RMVar_hsa_circ_347286,RMVar_hsa_circ_287448,RMVar_hsa_circ_228929,RMVar_hsa_circ_46775,RMVar_hsa_circ_228928,RMVar_hsa_circ_347126,RMVar_hsa_circ_376986,RMVar_hsa_circ_106561,RMVar_hsa_circ_267340,RMVar_hsa_circ_79527,RMVar_hsa_circ_50447,RMVar_hsa_circ_228931,RMVar_hsa_circ_228932,RMVar_hsa_circ_95410,RMVar_hsa_circ_127839,RMVar_hsa_circ_228933,RMVar_hsa_circ_228934,RMVar_hsa_circ_49876 21406 RMVar_ID_21406 Human_SNP_ID_207896077 A-to-I Human chr4 + 147912307 147912307 147912307 CACACCTGTAATCCCAGCACTTTGGGATGCCAAAGTGGTCAGATCACCTGAGGTCAGGAATTCAA CACACCTGTAATCCCAGCACTTTGGGATGCCAGAGTGGTCAGATCACCTGAGGTCAGGAATTCAA A G ARHGAP10 Ensembl:ENSG00000071205 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1465010862 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37033,RMVar_hsa_circ_100243,RMVar_hsa_circ_347626,RMVar_hsa_circ_121902,RMVar_hsa_circ_228917,RMVar_hsa_circ_228916,RMVar_hsa_circ_228924,RMVar_hsa_circ_72206,RMVar_hsa_circ_228923,RMVar_hsa_circ_103665,RMVar_hsa_circ_33616,RMVar_hsa_circ_349672,RMVar_hsa_circ_354540,RMVar_hsa_circ_351827,RMVar_hsa_circ_347286,RMVar_hsa_circ_287448,RMVar_hsa_circ_228929,RMVar_hsa_circ_46775,RMVar_hsa_circ_228928,RMVar_hsa_circ_347126,RMVar_hsa_circ_376986,RMVar_hsa_circ_106561,RMVar_hsa_circ_267340,RMVar_hsa_circ_79527,RMVar_hsa_circ_50447,RMVar_hsa_circ_228931,RMVar_hsa_circ_228932,RMVar_hsa_circ_95410,RMVar_hsa_circ_127839,RMVar_hsa_circ_228933,RMVar_hsa_circ_228934,RMVar_hsa_circ_66051,RMVar_hsa_circ_228937,RMVar_hsa_circ_13132,RMVar_hsa_circ_107190,RMVar_hsa_circ_303754,RMVar_hsa_circ_328665,RMVar_hsa_circ_354715,RMVar_hsa_circ_319299,RMVar_hsa_circ_289271,RMVar_hsa_circ_47608,RMVar_hsa_circ_228939,RMVar_hsa_circ_228941,RMVar_hsa_circ_228942,RMVar_hsa_circ_228940,RMVar_hsa_circ_228938,RMVar_hsa_circ_111243,RMVar_hsa_circ_309582,RMVar_hsa_circ_228936,RMVar_hsa_circ_341450,RMVar_hsa_circ_307199,RMVar_hsa_circ_76535,RMVar_hsa_circ_228944,RMVar_hsa_circ_39190,RMVar_hsa_circ_228945,RMVar_hsa_circ_228943 21407 RMVar_ID_21407 Human_SNP_ID_207911407 A-to-I Human chr4 + 147974760 147974760 147974760 GATAAAGACATACCCAAGACTGGGAAATTTACAAATGAAAGAGGTTTAATGGGCTCATGGTTCCA GATAAAGACATACCCAAGACTGGGAAATTTACCAATGAAAGAGGTTTAATGGGCTCATGGTTCCA A C ARHGAP10 Ensembl:ENSG00000071205 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1352477777 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_107190,RMVar_hsa_circ_354715,RMVar_hsa_circ_47608,RMVar_hsa_circ_228941,RMVar_hsa_circ_228942,RMVar_hsa_circ_111243,RMVar_hsa_circ_76535,RMVar_hsa_circ_24369,RMVar_hsa_circ_300736,RMVar_hsa_circ_228944,RMVar_hsa_circ_228943,RMVar_hsa_circ_314784,RMVar_hsa_circ_228949,RMVar_hsa_circ_305386,RMVar_hsa_circ_31096,RMVar_hsa_circ_228951,RMVar_hsa_circ_312575,RMVar_hsa_circ_348149 21408 RMVar_ID_21408 Human_SNP_ID_207911408 A-to-I Human chr4 + 147974760 147974760 147974760 GATAAAGACATACCCAAGACTGGGAAATTTACAAATGAAAGAGGTTTAATGGGCTCATGGTTCCA GATAAAGACATACCCAAGACTGGGAAATTTACGAATGAAAGAGGTTTAATGGGCTCATGGTTCCA A G ARHGAP10 Ensembl:ENSG00000071205 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1352477777 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_107190,RMVar_hsa_circ_354715,RMVar_hsa_circ_47608,RMVar_hsa_circ_228941,RMVar_hsa_circ_228942,RMVar_hsa_circ_111243,RMVar_hsa_circ_76535,RMVar_hsa_circ_24369,RMVar_hsa_circ_300736,RMVar_hsa_circ_228944,RMVar_hsa_circ_228943,RMVar_hsa_circ_314784,RMVar_hsa_circ_228949,RMVar_hsa_circ_305386,RMVar_hsa_circ_31096,RMVar_hsa_circ_228951,RMVar_hsa_circ_312575,RMVar_hsa_circ_348149 21409 RMVar_ID_21409 Human_SNP_ID_245064242 A-to-I Human chr5 - 107627592 107627588 107627593 TTGATCTGTCACCCAGGTTGGAGTGCAATGGCACAATCATAGCTCACAGCAACCTCGAACTCCTG TTGATCTGTCACCCAGGTTGGAGTGCAATGG_____TCATAGCTCACAGCAACCTCGAACTCCTG ATTGTG A EFNA5 Ensembl:ENSG00000184349 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1488410525 Functional Loss DEL dbSNP153 32..36 33 - - - Human_RBP_ID_23036756,Human_RBP_ID_25935075 21410 RMVar_ID_21410 Human_SNP_ID_245089792 A-to-I Human chr5 - 107725323 107725323 107725323 TTGTCATCTTCTATAAATCCTTTCTCAGGATCAGTCACTTCACTCCAGGCCATAAAATTGGAAAA TTGTCATCTTCTATAAATCCTTTCTCAGGATCGGTCACTTCACTCCAGGCCATAAAATTGGAAAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1341608495 Functional Loss SNV dbSNP153 33..33 33 - - - 21411 RMVar_ID_21411 Human_SNP_ID_245090186 A-to-I Human chr5 + 107726630 107726630 107726630 TGAGTTTGTTCAGAACCTCTCTCAGATCATGGAATTTCCACAAGATCAAATTCAATTGTGGCCCA TGAGTTTGTTCAGAACCTCTCTCAGATCATGGGATTTCCACAAGATCAAATTCAATTGTGGCCCA A G AC024587.1 Ensembl:ENSG00000248827 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1465541087 Functional Loss SNV dbSNP153 33..33 33 - - - 21412 RMVar_ID_21412 Human_SNP_ID_245200586 A-to-I Human chr5 - 108162409 108162409 108162409 TCACTGTAACCTTGAACTTGTGGGCTCAAGCAATCCTCCTGCTTCAGTCTCCCGAGTAGCTGGGA TCACTGTAACCTTGAACTTGTGGGCTCAAGCAGTCCTCCTGCTTCAGTCTCCCGAGTAGCTGGGA T C FBXL17 Ensembl:ENSG00000145743 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs529377686 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19287,RMVar_hsa_circ_120981,RMVar_hsa_circ_36759,RMVar_hsa_circ_233550,RMVar_hsa_circ_233552,RMVar_hsa_circ_284165,RMVar_hsa_circ_316794,RMVar_hsa_circ_308505,RMVar_hsa_circ_279823,RMVar_hsa_circ_233553 21413 RMVar_ID_21413 Human_SNP_ID_245200587 A-to-I Human chr5 - 108162413 108162413 108162413 TACGTCACTGTAACCTTGAACTTGTGGGCTCAAGCAATCCTCCTGCTTCAGTCTCCCGAGTAGCT TACGTCACTGTAACCTTGAACTTGTGGGCTCAGGCAATCCTCCTGCTTCAGTCTCCCGAGTAGCT T C FBXL17 Ensembl:ENSG00000145743 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1337701656 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19287,RMVar_hsa_circ_120981,RMVar_hsa_circ_36759,RMVar_hsa_circ_233550,RMVar_hsa_circ_233552,RMVar_hsa_circ_284165,RMVar_hsa_circ_316794,RMVar_hsa_circ_308505,RMVar_hsa_circ_279823,RMVar_hsa_circ_233553 21414 RMVar_ID_21414 Human_SNP_ID_245360593 A-to-I Human chr5 + 108764853 108764853 108764853 TAGAGATGGGAAAGAGAAGTAGAGCCAGGACTAGGGTAAGGCAAGAGAGTTGCCTAGGACACAAA TAGAGATGGGAAAGAGAAGTAGAGCCAGGACTCGGGTAAGGCAAGAGAGTTGCCTAGGACACAAA A C FER Ensembl:ENSG00000151422 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973528651 Functional Loss SNV dbSNP153 33..33 33 - - - 21415 RMVar_ID_21415 Human_SNP_ID_245365640 A-to-I Human chr5 - 108785098 108785098 108785098 ACCTTGACCAGCTTGTCCCAGCTACAGGAGACAGTGATAGGGTTGCTGCTGTTAGGCAAGAAGCG ACCTTGACCAGCTTGTCCCAGCTACAGGAGACGGTGATAGGGTTGCTGCTGTTAGGCAAGAAGCG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879230548 Functional Loss SNV dbSNP153 33..33 33 - - - 21416 RMVar_ID_21416 Human_SNP_ID_245365649 A-to-I Human chr5 - 108785137 108785137 108785137 ATGTGGTTGGTCTTCAGCTTGCAGTTAGCCAGATTCCATACCTTGACCAGCTTGTCCCAGCTACA ATGTGGTTGGTCTTCAGCTTGCAGTTAGCCAGGTTCCATACCTTGACCAGCTTGTCCCAGCTACA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560045904 Functional Loss SNV dbSNP153 33..33 33 - - - 21417 RMVar_ID_21417 Human_SNP_ID_245365668 A-to-I Human chr5 - 108785194 108785194 108785194 GCACAGAGGGATCCATTTGGAGACATAGTCACAGTGTTCAGATAACCTGTGTGGCCAATGTGGTT GCACAGAGGGATCCATTTGGAGACATAGTCACCGTGTTCAGATAACCTGTGTGGCCAATGTGGTT T G - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs990270631 Functional Loss SNV dbSNP153 33..33 33 - - - 21418 RMVar_ID_21418 Human_SNP_ID_245365691 A-to-I Human chr5 - 108785287 108785287 108785287 AGGGTGTTGATAATGCCCCCACCATCTGGCATATAAAGGTGTTTGCCTTCGTTGAGATCCCACAG AGGGTGTTGATAATGCCCCCACCATCTGGCATGTAAAGGTGTTTGCCTTCGTTGAGATCCCACAG T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1045620805 Functional Loss SNV dbSNP153 33..33 33 - - - 21419 RMVar_ID_21419 Human_SNP_ID_245365692 A-to-I Human chr5 - 108785289 108785289 108785289 ACAGGGTGTTGATAATGCCCCCACCATCTGGCATATAAAGGTGTTTGCCTTCGTTGAGATCCCAC ACAGGGTGTTGATAATGCCCCCACCATCTGGCGTATAAAGGTGTTTGCCTTCGTTGAGATCCCAC T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs907110638 Functional Loss SNV dbSNP153 33..33 33 - - - 21420 RMVar_ID_21420 Human_SNP_ID_245394522 A-to-I Human chr5 + 108894479 108894479 108894479 ATGAAGCAGTTCTTCACTGATAACATGTGAGGATATTTCTCAGAGTCTATGACACTGATATTAGT ATGAAGCAGTTCTTCACTGATAACATGTGAGGGTATTTCTCAGAGTCTATGACACTGATATTAGT A G FER Ensembl:ENSG00000151422 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs922011986 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38535,RMVar_hsa_circ_284672,RMVar_hsa_circ_311524,RMVar_hsa_circ_333145,RMVar_hsa_circ_303950,RMVar_hsa_circ_284745,RMVar_hsa_circ_47488,RMVar_hsa_circ_233572,RMVar_hsa_circ_298988,RMVar_hsa_circ_362966,RMVar_hsa_circ_363276,RMVar_hsa_circ_330117,RMVar_hsa_circ_72848,RMVar_hsa_circ_61279,RMVar_hsa_circ_233573,RMVar_hsa_circ_360580,RMVar_hsa_circ_312638,RMVar_hsa_circ_315102,RMVar_hsa_circ_309192,RMVar_hsa_circ_71525,RMVar_hsa_circ_20219,RMVar_hsa_circ_22458,RMVar_hsa_circ_30022,RMVar_hsa_circ_233579,RMVar_hsa_circ_325176,RMVar_hsa_circ_368658,RMVar_hsa_circ_309431,RMVar_hsa_circ_276737,RMVar_hsa_circ_297008,RMVar_hsa_circ_233583,RMVar_hsa_circ_233584,RMVar_hsa_circ_233585,RMVar_hsa_circ_338747,RMVar_hsa_circ_30205,RMVar_hsa_circ_233586,RMVar_hsa_circ_276781,RMVar_hsa_circ_60727,RMVar_hsa_circ_22400,RMVar_hsa_circ_327761,RMVar_hsa_circ_333573,RMVar_hsa_circ_333737,RMVar_hsa_circ_325926,RMVar_hsa_circ_233588,RMVar_hsa_circ_275124,RMVar_hsa_circ_233587 21421 RMVar_ID_21421 Human_SNP_ID_245394523 A-to-I Human chr5 + 108894490 108894490 108894490 CTTCACTGATAACATGTGAGGATATTTCTCAGAGTCTATGACACTGATATTAGTTAGTTTGATGT CTTCACTGATAACATGTGAGGATATTTCTCAGGGTCTATGACACTGATATTAGTTAGTTTGATGT A G FER Ensembl:ENSG00000151422 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277431633 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38535,RMVar_hsa_circ_284672,RMVar_hsa_circ_311524,RMVar_hsa_circ_333145,RMVar_hsa_circ_303950,RMVar_hsa_circ_284745,RMVar_hsa_circ_47488,RMVar_hsa_circ_233572,RMVar_hsa_circ_298988,RMVar_hsa_circ_362966,RMVar_hsa_circ_363276,RMVar_hsa_circ_330117,RMVar_hsa_circ_72848,RMVar_hsa_circ_61279,RMVar_hsa_circ_233573,RMVar_hsa_circ_360580,RMVar_hsa_circ_312638,RMVar_hsa_circ_315102,RMVar_hsa_circ_309192,RMVar_hsa_circ_71525,RMVar_hsa_circ_20219,RMVar_hsa_circ_22458,RMVar_hsa_circ_30022,RMVar_hsa_circ_233579,RMVar_hsa_circ_325176,RMVar_hsa_circ_368658,RMVar_hsa_circ_309431,RMVar_hsa_circ_276737,RMVar_hsa_circ_297008,RMVar_hsa_circ_233583,RMVar_hsa_circ_233584,RMVar_hsa_circ_233585,RMVar_hsa_circ_338747,RMVar_hsa_circ_30205,RMVar_hsa_circ_233586,RMVar_hsa_circ_276781,RMVar_hsa_circ_60727,RMVar_hsa_circ_22400,RMVar_hsa_circ_327761,RMVar_hsa_circ_333573,RMVar_hsa_circ_333737,RMVar_hsa_circ_325926,RMVar_hsa_circ_233588,RMVar_hsa_circ_275124,RMVar_hsa_circ_233587 21422 RMVar_ID_21422 Human_SNP_ID_245394526 A-to-I Human chr5 + 108894495 108894495 108894495 CTGATAACATGTGAGGATATTTCTCAGAGTCTATGACACTGATATTAGTTAGTTTGATGTTGAGA CTGATAACATGTGAGGATATTTCTCAGAGTCTGTGACACTGATATTAGTTAGTTTGATGTTGAGA A G FER Ensembl:ENSG00000151422 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs547656873 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38535,RMVar_hsa_circ_284672,RMVar_hsa_circ_311524,RMVar_hsa_circ_333145,RMVar_hsa_circ_303950,RMVar_hsa_circ_284745,RMVar_hsa_circ_47488,RMVar_hsa_circ_233572,RMVar_hsa_circ_298988,RMVar_hsa_circ_362966,RMVar_hsa_circ_363276,RMVar_hsa_circ_330117,RMVar_hsa_circ_72848,RMVar_hsa_circ_61279,RMVar_hsa_circ_233573,RMVar_hsa_circ_360580,RMVar_hsa_circ_312638,RMVar_hsa_circ_315102,RMVar_hsa_circ_309192,RMVar_hsa_circ_71525,RMVar_hsa_circ_20219,RMVar_hsa_circ_22458,RMVar_hsa_circ_30022,RMVar_hsa_circ_233579,RMVar_hsa_circ_325176,RMVar_hsa_circ_368658,RMVar_hsa_circ_309431,RMVar_hsa_circ_276737,RMVar_hsa_circ_297008,RMVar_hsa_circ_233583,RMVar_hsa_circ_233584,RMVar_hsa_circ_233585,RMVar_hsa_circ_338747,RMVar_hsa_circ_30205,RMVar_hsa_circ_233586,RMVar_hsa_circ_276781,RMVar_hsa_circ_60727,RMVar_hsa_circ_22400,RMVar_hsa_circ_327761,RMVar_hsa_circ_333573,RMVar_hsa_circ_333737,RMVar_hsa_circ_325926,RMVar_hsa_circ_233588,RMVar_hsa_circ_275124,RMVar_hsa_circ_233587 21423 RMVar_ID_21423 Human_SNP_ID_245394531 A-to-I Human chr5 + 108894506 108894506 108894506 TGAGGATATTTCTCAGAGTCTATGACACTGATATTAGTTAGTTTGATGTTGAGATACCGATCCAC TGAGGATATTTCTCAGAGTCTATGACACTGATGTTAGTTAGTTTGATGTTGAGATACCGATCCAC A G FER Ensembl:ENSG00000151422 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1436795790 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38535,RMVar_hsa_circ_284672,RMVar_hsa_circ_311524,RMVar_hsa_circ_333145,RMVar_hsa_circ_303950,RMVar_hsa_circ_284745,RMVar_hsa_circ_47488,RMVar_hsa_circ_233572,RMVar_hsa_circ_298988,RMVar_hsa_circ_362966,RMVar_hsa_circ_363276,RMVar_hsa_circ_330117,RMVar_hsa_circ_72848,RMVar_hsa_circ_61279,RMVar_hsa_circ_233573,RMVar_hsa_circ_360580,RMVar_hsa_circ_312638,RMVar_hsa_circ_315102,RMVar_hsa_circ_309192,RMVar_hsa_circ_71525,RMVar_hsa_circ_20219,RMVar_hsa_circ_22458,RMVar_hsa_circ_30022,RMVar_hsa_circ_233579,RMVar_hsa_circ_325176,RMVar_hsa_circ_368658,RMVar_hsa_circ_309431,RMVar_hsa_circ_276737,RMVar_hsa_circ_297008,RMVar_hsa_circ_233583,RMVar_hsa_circ_233584,RMVar_hsa_circ_233585,RMVar_hsa_circ_338747,RMVar_hsa_circ_30205,RMVar_hsa_circ_233586,RMVar_hsa_circ_276781,RMVar_hsa_circ_60727,RMVar_hsa_circ_22400,RMVar_hsa_circ_327761,RMVar_hsa_circ_333573,RMVar_hsa_circ_333737,RMVar_hsa_circ_325926,RMVar_hsa_circ_233588,RMVar_hsa_circ_275124,RMVar_hsa_circ_233587 21424 RMVar_ID_21424 Human_SNP_ID_245394568 A-to-I Human chr5 - 108894618 108894618 108894618 AGCCCGCAGGACCAGCACCACGCTCTTCTATTATTTTTTCAAGTCCCTTGAGGGCAAGCATGTGG AGCCCGCAGGACCAGCACCACGCTCTTCTATTCTTTTTTCAAGTCCCTTGAGGGCAAGCATGTGG T G AC109481.2 Ensembl:ENSG00000250441 Pseudogene exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs970871679 Functional Loss SNV dbSNP153 33..33 33 - - - 21425 RMVar_ID_21425 Human_SNP_ID_245409240 A-to-I Human chr5 + 108951298 108951298 108951298 AAAAATAAAAATAAAAATAAATTTCTAGAGATAGGGCCTCACTATGTTGTCCAGGCTGGTCTTGA AAAAATAAAAATAAAAATAAATTTCTAGAGATGGGGCCTCACTATGTTGTCCAGGCTGGTCTTGA A G FER Ensembl:ENSG00000151422 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973761221 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38535,RMVar_hsa_circ_284672,RMVar_hsa_circ_311524,RMVar_hsa_circ_284745,RMVar_hsa_circ_47488,RMVar_hsa_circ_233572,RMVar_hsa_circ_298988,RMVar_hsa_circ_363276,RMVar_hsa_circ_61279,RMVar_hsa_circ_233573,RMVar_hsa_circ_360580,RMVar_hsa_circ_315102,RMVar_hsa_circ_20219,RMVar_hsa_circ_22458,RMVar_hsa_circ_325176,RMVar_hsa_circ_368658,RMVar_hsa_circ_297008,RMVar_hsa_circ_233585,RMVar_hsa_circ_30205,RMVar_hsa_circ_233592,RMVar_hsa_circ_233586,RMVar_hsa_circ_276781,RMVar_hsa_circ_327761,RMVar_hsa_circ_275124,RMVar_hsa_circ_275419,RMVar_hsa_circ_316347,RMVar_hsa_circ_233590,RMVar_hsa_circ_283711,RMVar_hsa_circ_315234,RMVar_hsa_circ_233591,RMVar_hsa_circ_289509,RMVar_hsa_circ_233593 21426 RMVar_ID_21426 Human_SNP_ID_245456276 A-to-I Human chr5 + 109124001 109124001 109124001 CCTGTAATCCCAGCACTTTGGGAGACCGAGGTAGATCACTGAGTCCAGGAGTTTGAGTCTAACCT CCTGTAATCCCAGCACTTTGGGAGACCGAGGTCGATCACTGAGTCCAGGAGTTTGAGTCTAACCT A C FER Ensembl:ENSG00000151422 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1176186750 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47488,RMVar_hsa_circ_369165 21427 RMVar_ID_21427 Human_SNP_ID_245529858 A-to-I Human chr5 - 109394188 109394188 109394188 CAAAAATTATCCAGGCATGGTGGCGGGTACCTATAATCCCAGCTACTCGGGAGGCTGAGGCAGGA CAAAAATTATCCAGGCATGGTGGCGGGTACCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGA T C PJA2 Ensembl:ENSG00000198961 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1240396947 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95556,RMVar_hsa_circ_233607 21428 RMVar_ID_21428 Human_SNP_ID_245529864 A-to-I Human chr5 - 109394204 109394204 109394204 ATCTCTACTAAAAATACAAAAATTATCCAGGCATGGTGGCGGGTACCTATAATCCCAGCTACTCG ATCTCTACTAAAAATACAAAAATTATCCAGGCGTGGTGGCGGGTACCTATAATCCCAGCTACTCG T C PJA2 Ensembl:ENSG00000198961 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1333204598 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95556,RMVar_hsa_circ_233607 21429 RMVar_ID_21429 Human_SNP_ID_245529865 A-to-I Human chr5 - 109394208 109394208 109394208 CCCCATCTCTACTAAAAATACAAAAATTATCCAGGCATGGTGGCGGGTACCTATAATCCCAGCTA CCCCATCTCTACTAAAAATACAAAAATTATCCGGGCATGGTGGCGGGTACCTATAATCCCAGCTA T C PJA2 Ensembl:ENSG00000198961 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1272907968 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95556,RMVar_hsa_circ_233607 21430 RMVar_ID_21430 Human_SNP_ID_245529874 A-to-I Human chr5 - 109394230 109394230 109394230 CAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTATCCAGGCATGGTGG CAGCCTGGCCAACATGGTGAAACCCCATCTCTGCTAAAAATACAAAAATTATCCAGGCATGGTGG T C PJA2 Ensembl:ENSG00000198961 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1322410437 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95556,RMVar_hsa_circ_233607 21431 RMVar_ID_21431 Human_SNP_ID_245529875 A-to-I Human chr5 - 109394230 109394230 109394230 CAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTATCCAGGCATGGTGG CAGCCTGGCCAACATGGTGAAACCCCATCTCTCCTAAAAATACAAAAATTATCCAGGCATGGTGG T G PJA2 Ensembl:ENSG00000198961 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1322410437 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95556,RMVar_hsa_circ_233607 21432 RMVar_ID_21432 Human_SNP_ID_245529880 A-to-I Human chr5 - 109394272 109394272 109394272 AGGCGGAGGCGGGTGGATCACTTAAGGTCAGGAGTTTGAGATCAGCCTGGCCAACATGGTGAAAC AGGCGGAGGCGGGTGGATCACTTAAGGTCAGGGGTTTGAGATCAGCCTGGCCAACATGGTGAAAC T C PJA2 Ensembl:ENSG00000198961 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1416863887 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95556,RMVar_hsa_circ_233607 21433 RMVar_ID_21433 Human_SNP_ID_245616769 A-to-I Human chr5 + 109715720 109715720 109715720 ACATGAGATTTACTATAAAATAAAGATAGCACAAAGTAAAATATCATTTTCAGAACTGTTTTTGA ACATGAGATTTACTATAAAATAAAGATAGCACGAAGTAAAATATCATTTTCAGAACTGTTTTTGA A G MAN2A1 Ensembl:ENSG00000112893 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs149217838 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14981,RMVar_hsa_circ_233614,RMVar_hsa_circ_233616,RMVar_hsa_circ_233615,RMVar_hsa_circ_271542,RMVar_hsa_circ_289233,RMVar_hsa_circ_305352,RMVar_hsa_circ_310768,RMVar_hsa_circ_323152,RMVar_hsa_circ_372676,RMVar_hsa_circ_306289,RMVar_hsa_circ_295998,RMVar_hsa_circ_275487,RMVar_hsa_circ_280636,RMVar_hsa_circ_273112,RMVar_hsa_circ_93485,RMVar_hsa_circ_103363,RMVar_hsa_circ_85624,RMVar_hsa_circ_233619,RMVar_hsa_circ_233623,RMVar_hsa_circ_233627,RMVar_hsa_circ_233629,RMVar_hsa_circ_233630,RMVar_hsa_circ_233631,RMVar_hsa_circ_233628,RMVar_hsa_circ_233625,RMVar_hsa_circ_233626,RMVar_hsa_circ_233624,RMVar_hsa_circ_233621,RMVar_hsa_circ_233622,RMVar_hsa_circ_233620,RMVar_hsa_circ_233617,RMVar_hsa_circ_233618 21434 RMVar_ID_21434 Human_SNP_ID_245639471 A-to-I Human chr5 + 109799967 109799967 109799967 AAAATTAGCCGGGAGTGGTAGCATGCACCTGTAATCCCTGCTACTTGGGAGACTGAGGCAGGAGA AAAATTAGCCGGGAGTGGTAGCATGCACCTGTGATCCCTGCTACTTGGGAGACTGAGGCAGGAGA A G MAN2A1 Ensembl:ENSG00000112893 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1012503297 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33556,RMVar_hsa_circ_289233,RMVar_hsa_circ_305352,RMVar_hsa_circ_280636,RMVar_hsa_circ_93485,RMVar_hsa_circ_103363,RMVar_hsa_circ_85624,RMVar_hsa_circ_233619,RMVar_hsa_circ_233621,RMVar_hsa_circ_233622,RMVar_hsa_circ_233620,RMVar_hsa_circ_233617,RMVar_hsa_circ_233618,RMVar_hsa_circ_344958,RMVar_hsa_circ_8094,RMVar_hsa_circ_332925,RMVar_hsa_circ_359922,RMVar_hsa_circ_335462,RMVar_hsa_circ_280573,RMVar_hsa_circ_122024,RMVar_hsa_circ_268445,RMVar_hsa_circ_62381,RMVar_hsa_circ_233643,RMVar_hsa_circ_233645,RMVar_hsa_circ_233646,RMVar_hsa_circ_233644,RMVar_hsa_circ_233642,RMVar_hsa_circ_233647,RMVar_hsa_circ_333261,RMVar_hsa_circ_266521,RMVar_hsa_circ_375968,RMVar_hsa_circ_20119,RMVar_hsa_circ_233650,RMVar_hsa_circ_278765,RMVar_hsa_circ_233652,RMVar_hsa_circ_233653,RMVar_hsa_circ_357423,RMVar_hsa_circ_233654,RMVar_hsa_circ_357467,RMVar_hsa_circ_54592,RMVar_hsa_circ_118257,RMVar_hsa_circ_233655 21435 RMVar_ID_21435 Human_SNP_ID_245827881 A-to-I Human chr5 - 110433985 110433985 110433985 AAAGATACCTCCTTAACTCATTCTATAATACTAGTATCATCCTGATACCAAAATCTGGCAAAGAC AAAGATACCTCCTTAACTCATTCTATAATACTGGTATCATCCTGATACCAAAATCTGGCAAAGAC T C TMEM232 Ensembl:ENSG00000186952 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs867369785 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_289654,RMVar_hsa_circ_1198 21436 RMVar_ID_21436 Human_SNP_ID_245969650 A-to-I Human chr5 + 110948239 110948239 110948239 TTGGTCTAATAATCCACACCATCATCTCTGTCATGATGCAAGAAATACTTCTTGCTCTTTGGGAT TTGGTCTAATAATCCACACCATCATCTCTGTCGTGATGCAAGAAATACTTCTTGCTCTTTGGGAT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs866128908 Functional Loss SNV dbSNP153 33..33 33 - - - 21437 RMVar_ID_21437 Human_SNP_ID_246022386 A-to-I Human chr5 + 111121023 111121023 111121023 TTAAGATGTAGAAGTATCAGAAGAAACAGTAGAACCAAGTGATGAATTGATAGAATATGATTCGC TTAAGATGTAGAAGTATCAGAAGAAACAGTAGGACCAAGTGATGAATTGATAGAATATGATTCGC A G WDR36 Ensembl:ENSG00000134987 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1157237590 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1984147,Human_RBP_ID_3753255,Human_RBP_ID_15262871 Human_Splice_Rec_679800,Human_Splice_Rec_679844,Human_Splice_Rec_679888 Human_miRNA_ID_1039503,Human_miRNA_ID_2478587 RMVar_hsa_circ_18087,RMVar_hsa_circ_7141,RMVar_hsa_circ_35558,RMVar_hsa_circ_67028,RMVar_hsa_circ_39051,RMVar_hsa_circ_29066 21438 RMVar_ID_21438 Human_SNP_ID_246079085 A-to-I Human chr5 + 111330790 111330790 111330790 AAATCAGAGTAGTGAGGCGTTGGCATAACAATAGAGAGAATAGAGTCCTGGCACAGATCCATAGA AAATCAGAGTAGTGAGGCGTTGGCATAACAATGGAGAGAATAGAGTCCTGGCACAGATCCATAGA A G CAMK4 Ensembl:ENSG00000152495 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1047680686 Functional Loss SNV dbSNP153 33..33 33 - - - 21439 RMVar_ID_21439 Human_SNP_ID_246122949 A-to-I Human chr5 - 111499562 111499562 111499562 ATTCTACCTCAGCCTCCTGAATAGCTGGGAATACAGGTGCACGCCACTATGCATGGCTAATTTTT ATTCTACCTCAGCCTCCTGAATAGCTGGGAATGCAGGTGCACGCCACTATGCATGGCTAATTTTT T C STARD4 Ensembl:ENSG00000164211 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1391020913 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_628449,Human_RBP_ID_4803653,Human_RBP_ID_7364366 Human_miRNA_ID_1400358,Human_miRNA_ID_1473236 21440 RMVar_ID_21440 Human_SNP_ID_246125514 A-to-I Human chr5 - 111509786 111509786 111509786 AGCTCTAGGATTGGCGTAAATGGGCATACTTTAGATATCTTGAGGTCTTCCATAAGTGAGAATGG AGCTCTAGGATTGGCGTAAATGGGCATACTTTGGATATCTTGAGGTCTTCCATAAGTGAGAATGG T C STARD4 Ensembl:ENSG00000164211 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs896527132 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7364410 RMVar_hsa_circ_94620,RMVar_hsa_circ_233706 21441 RMVar_ID_21441 Human_SNP_ID_246125530 A-to-I Human chr5 - 111509825 111509825 111509825 GGTGTTTCATTATGGTAAAGGAAGTTTTAGTTATTCAGAAGCTCTAGGATTGGCGTAAATGGGCA GGTGTTTCATTATGGTAAAGGAAGTTTTAGTTGTTCAGAAGCTCTAGGATTGGCGTAAATGGGCA T C STARD4 Ensembl:ENSG00000164211 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs952671635 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94620,RMVar_hsa_circ_233706 21442 RMVar_ID_21442 Human_SNP_ID_246125865 A-to-I Human chr5 - 111511545 111511545 111511545 TTCTGTAAAACAGGGAAAATGTATAGACATTAAGCTACTATTCTCACTTATGGAAGACCTCAAGA TTCTGTAAAACAGGGAAAATGTATAGACATTAGGCTACTATTCTCACTTATGGAAGACCTCAAGA T C STARD4 Ensembl:ENSG00000164211 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1294611903 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94620,RMVar_hsa_circ_233706 21443 RMVar_ID_21443 Human_SNP_ID_246307584 A-to-I Human chr5 + 112164030 112164030 112164030 CCTGTAGATTGCAAAGTCATCTATGGAGAGGAAAGGTACAAAATAGTCACTGGGGAGAGCAGGTG CCTGTAGATTGCAAAGTCATCTATGGAGAGGAGAGGTACAAAATAGTCACTGGGGAGAGCAGGTG A G EPB41L4A-AS1 Ensembl:ENSG00000224032 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1321471231 Functional Loss SNV dbSNP153 33..33 33 - - - 21444 RMVar_ID_21444 Human_SNP_ID_246352782 A-to-I Human chr5 - 112329747 112329747 112329747 ACAATGGCTTAGGTGTACTCAGATCCATTCACACCCCCTTTTTCCTGTAGAGAGTGACATGGATT ACAATGGCTTAGGTGTACTCAGATCCATTCACGCCCCCTTTTTCCTGTAGAGAGTGACATGGATT T C EPB41L4A Ensembl:ENSG00000129595 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs907329213 Functional Loss SNV dbSNP153 33..33 33 - - - 21445 RMVar_ID_21445 Human_SNP_ID_246352783 A-to-I Human chr5 - 112329757 112329757 112329757 TATTTCCCCCACAATGGCTTAGGTGTACTCAGATCCATTCACACCCCCTTTTTCCTGTAGAGAGT TATTTCCCCCACAATGGCTTAGGTGTACTCAGGTCCATTCACACCCCCTTTTTCCTGTAGAGAGT T C EPB41L4A Ensembl:ENSG00000129595 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs997117503 Functional Loss SNV dbSNP153 33..33 33 - - - 21446 RMVar_ID_21446 Human_SNP_ID_246352784 A-to-I Human chr5 - 112329763 112329763 112329763 TGAAAGTATTTCCCCCACAATGGCTTAGGTGTACTCAGATCCATTCACACCCCCTTTTTCCTGTA TGAAAGTATTTCCCCCACAATGGCTTAGGTGTGCTCAGATCCATTCACACCCCCTTTTTCCTGTA T C EPB41L4A Ensembl:ENSG00000129595 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335724359 Functional Loss SNV dbSNP153 33..33 33 - - - 21447 RMVar_ID_21447 Human_SNP_ID_246364321 A-to-I Human chr5 - 112370162 112370162 112370162 AAATTAGACAGGCTTGGTGGTGTGTACCTGTTATCCCAGTTACTCAGGAGGCTGAGACAAGAAGA AAATTAGACAGGCTTGGTGGTGTGTACCTGTTTTCCCAGTTACTCAGGAGGCTGAGACAAGAAGA T A EPB41L4A Ensembl:ENSG00000129595 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270518617 Functional Loss SNV dbSNP153 33..33 33 - - - 21448 RMVar_ID_21448 Human_SNP_ID_246463421 A-to-I Human chr5 + 112712893 112712893 112712893 AGTTAACATTGATTTAAACAGTATCTCGGGCTAGGCGCTGTGGCTCACGCCTGTAATCCCAGCAC AGTTAACATTGATTTAAACAGTATCTCGGGCTGGGCGCTGTGGCTCACGCCTGTAATCCCAGCAC A G APC Ensembl:ENSG00000134982 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1300558257 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107256,RMVar_hsa_circ_233748 21449 RMVar_ID_21449 Human_SNP_ID_246509403 A-to-I Human chr5 + 112866530 112866528 112866530 TTTTTTATTTTTTCTAGAGATGGGGTTTTGCTATGTTTCCTAAGCCAGTCTCAAACTCGTGGACA TTTTTTATTTTTTCTAGAGATGGGGTTTTGC__TGTTTCCTAAGCCAGTCTCAAACTCGTGGACA CTA C AC008575.1,SRP19 Ensembl:ENSG00000258864,Ensembl:ENSG00000153037 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1370073508 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_15264738 21450 RMVar_ID_21450 Human_SNP_ID_246509405 A-to-I Human chr5 + 112866530 112866530 112866530 TTTTTTATTTTTTCTAGAGATGGGGTTTTGCTATGTTTCCTAAGCCAGTCTCAAACTCGTGGACA TTTTTTATTTTTTCTAGAGATGGGGTTTTGCTGTGTTTCCTAAGCCAGTCTCAAACTCGTGGACA A G AC008575.1,SRP19 Ensembl:ENSG00000258864,Ensembl:ENSG00000153037 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs979035435 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15264738 21451 RMVar_ID_21451 Human_SNP_ID_246513390 A-to-I Human chr5 - 112879748 112879748 112879748 GAAGAGGCCGGGCATGGTGGCTTACGTCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGCAGA GAAGAGGCCGGGCATGGTGGCTTACGTCTGTAGTCCCAGCACTTTGGGAGGCCAAGGCGGGCAGA T C REEP5 Ensembl:ENSG00000129625 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1367052733 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_233794,RMVar_hsa_circ_104264 21452 RMVar_ID_21452 Human_SNP_ID_246517820 A-to-I Human chr5 + 112895112 112895112 112895112 TAGAAAAAAAATAGCCGGGCATTGTGGTGGGCACCCGTAGTCCCAGCCACTCAGGAGGCTGAGGC TAGAAAAAAAATAGCCGGGCATTGTGGTGGGCGCCCGTAGTCCCAGCCACTCAGGAGGCTGAGGC A G SRP19 Ensembl:ENSG00000153037 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs112252664 Functional Loss SNV dbSNP153 33..33 33 - - - 21453 RMVar_ID_21453 Human_SNP_ID_246517825 A-to-I Human chr5 + 112895128 112895128 112895128 GGGCATTGTGGTGGGCACCCGTAGTCCCAGCCACTCAGGAGGCTGAGGCAGGAGAATCACTGGAA GGGCATTGTGGTGGGCACCCGTAGTCCCAGCCCCTCAGGAGGCTGAGGCAGGAGAATCACTGGAA A C SRP19 Ensembl:ENSG00000153037 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs747527367 Functional Loss SNV dbSNP153 33..33 33 - - - 21454 RMVar_ID_21454 Human_SNP_ID_246517828 A-to-I Human chr5 + 112895132 112895132 112895132 ATTGTGGTGGGCACCCGTAGTCCCAGCCACTCAGGAGGCTGAGGCAGGAGAATCACTGGAACCCA ATTGTGGTGGGCACCCGTAGTCCCAGCCACTCGGGAGGCTGAGGCAGGAGAATCACTGGAACCCA A G SRP19 Ensembl:ENSG00000153037 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1396951310 Functional Loss SNV dbSNP153 33..33 33 - - - 21455 RMVar_ID_21455 Human_SNP_ID_246519453 A-to-I Human chr5 - 112900986 112900984 112900986 AAAATACAAACGAAATTAGCTGGGTGTGGCAGAGTGCACCTGTAGTCCCAGCTACTCAGGAGGTG AAAATACAAACGAAATTAGCTGGGTGTGGCAG__TGCACCTGTAGTCCCAGCTACTCAGGAGGTG ACT A REEP5 Ensembl:ENSG00000129625 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs551893869 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_233794,RMVar_hsa_circ_104264,RMVar_hsa_circ_344625 21456 RMVar_ID_21456 Human_SNP_ID_246551440 A-to-I Human chr5 + 113004531 113004531 113004531 AGCACCACAGTTTATTTATTCATAACACTGTTAATGCACATTTTGGTTGTTTCCAGTTTGGGGCT AGCACCACAGTTTATTTATTCATAACACTGTTTATGCACATTTTGGTTGTTTCCAGTTTGGGGCT A T DCP2 Ensembl:ENSG00000172795 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs566551769 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_233801,RMVar_hsa_circ_284096,RMVar_hsa_circ_320565,RMVar_hsa_circ_233803,RMVar_hsa_circ_233802,RMVar_hsa_circ_115356,RMVar_hsa_circ_233804,RMVar_hsa_circ_362323,RMVar_hsa_circ_46043,RMVar_hsa_circ_37942 21457 RMVar_ID_21457 Human_SNP_ID_246552376 A-to-I Human chr5 + 113007058 113007057 113007058 TGCTTGGGAGGCTGAGGCAGGAGAATCGCTTGAACTTGGGAGGTGGAGGTTGCAGAGAGCCAAGC TGCTTGGGAGGCTGAGGCAGGAGAATCGCTTG_ACTTGGGAGGTGGAGGTTGCAGAGAGCCAAGC GA G DCP2 Ensembl:ENSG00000172795 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs35322144 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_25844414 RMVar_hsa_circ_233801,RMVar_hsa_circ_284096,RMVar_hsa_circ_320565,RMVar_hsa_circ_233803,RMVar_hsa_circ_233802,RMVar_hsa_circ_115356,RMVar_hsa_circ_233804,RMVar_hsa_circ_362323,RMVar_hsa_circ_46043,RMVar_hsa_circ_37942 21458 RMVar_ID_21458 Human_SNP_ID_246564874 A-to-I Human chr5 - 113046301 113046301 113046301 GTAATCCCAGCTACTCGGGAGGCTGCGGCACAAGAACTGCTTGAACCTGGGAGGCGGAAGTTGCA GTAATCCCAGCTACTCGGGAGGCTGCGGCACAGGAACTGCTTGAACCTGGGAGGCGGAAGTTGCA T C MCC Ensembl:ENSG00000171444 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1458207317 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9790,RMVar_hsa_circ_72319,RMVar_hsa_circ_114857,RMVar_hsa_circ_268342,RMVar_hsa_circ_233813,RMVar_hsa_circ_325108,RMVar_hsa_circ_27566,RMVar_hsa_circ_233814 21459 RMVar_ID_21459 Human_SNP_ID_247191561 A-to-I Human chr5 - 115205879 115205879 115205879 CAAAAATATTGCTGTGAGATCCTTGAAAATGTATAATTGCCCATTTGCATGTTTCTTTAAATTTA CAAAAATATTGCTGTGAGATCCTTGAAAATGTGTAATTGCCCATTTGCATGTTTCTTTAAATTTA T C PGGT1B Ensembl:ENSG00000164219 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs956734994 Functional Loss SNV dbSNP153 33..33 33 - - - 21460 RMVar_ID_21460 Human_SNP_ID_247191563 A-to-I Human chr5 - 115205883 115205883 115205883 ACTACAAAAATATTGCTGTGAGATCCTTGAAAATGTATAATTGCCCATTTGCATGTTTCTTTAAA ACTACAAAAATATTGCTGTGAGATCCTTGAAAGTGTATAATTGCCCATTTGCATGTTTCTTTAAA T C PGGT1B Ensembl:ENSG00000164219 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs955514367 Functional Loss SNV dbSNP153 33..33 33 - - - 21461 RMVar_ID_21461 Human_SNP_ID_247191570 A-to-I Human chr5 - 115205904 115205904 115205904 ATCAGTGCCTTATTTTTCACAACTACAAAAATATTGCTGTGAGATCCTTGAAAATGTATAATTGC ATCAGTGCCTTATTTTTCACAACTACAAAAATGTTGCTGTGAGATCCTTGAAAATGTATAATTGC T C PGGT1B Ensembl:ENSG00000164219 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs1320214837 Functional Loss SNV dbSNP153 33..33 33 - - - 21462 RMVar_ID_21462 Human_SNP_ID_247191789 A-to-I Human chr5 - 115206680 115206680 115206680 ATTTTCAAGGATCTCACAGCCACATTTTTGTAATTGTGAAAAATAAGACACATTATGATACATTT ATTTTCAAGGATCTCACAGCCACATTTTTGTAGTTGTGAAAAATAAGACACATTATGATACATTT T C PGGT1B Ensembl:ENSG00000164219 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs1446346658 Functional Loss SNV dbSNP153 33..33 33 - - - 21463 RMVar_ID_21463 Human_SNP_ID_247191791 A-to-I Human chr5 - 115206689 115206689 115206689 CAATGATACATTTTCAAGGATCTCACAGCCACATTTTTGTAATTGTGAAAAATAAGACACATTAT CAATGATACATTTTCAAGGATCTCACAGCCACGTTTTTGTAATTGTGAAAAATAAGACACATTAT T C PGGT1B Ensembl:ENSG00000164219 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1206866248 Functional Loss SNV dbSNP153 33..33 33 - - - 21464 RMVar_ID_21464 Human_SNP_ID_247191802 A-to-I Human chr5 - 115206726 115206726 115206726 TATCTATAGATTTAGCATAAAGAAACATGCAAATAGGCAATGATACATTTTCAAGGATCTCACAG TATCTATAGATTTAGCATAAAGAAACATGCAATTAGGCAATGATACATTTTCAAGGATCTCACAG T A PGGT1B Ensembl:ENSG00000164219 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1459307017 Functional Loss SNV dbSNP153 33..33 33 - - - 21465 RMVar_ID_21465 Human_SNP_ID_247191803 A-to-I Human chr5 - 115206727 115206727 115206727 CTATCTATAGATTTAGCATAAAGAAACATGCAAATAGGCAATGATACATTTTCAAGGATCTCACA CTATCTATAGATTTAGCATAAAGAAACATGCAGATAGGCAATGATACATTTTCAAGGATCTCACA T C PGGT1B Ensembl:ENSG00000164219 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229,31158229 RNA-Seq:(High) rs752755508 Functional Loss SNV dbSNP153 33..33 33 - - - 21466 RMVar_ID_21466 Human_SNP_ID_247191809 A-to-I Human chr5 - 115206753 115206753 115206753 TGCACACTTTTTGGCCCAGATACTCTCTATCTATAGATTTAGCATAAAGAAACATGCAAATAGGC TGCACACTTTTTGGCCCAGATACTCTCTATCTGTAGATTTAGCATAAAGAAACATGCAAATAGGC T C PGGT1B Ensembl:ENSG00000164219 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs921839314 Functional Loss SNV dbSNP153 33..33 33 - - - 21467 RMVar_ID_21467 Human_SNP_ID_247191825 A-to-I Human chr5 - 115206780 115206780 115206780 CAGAAGCTATCAGAATTTTTTAAAGTGTGCACACTTTTTGGCCCAGATACTCTCTATCTATAGAT CAGAAGCTATCAGAATTTTTTAAAGTGTGCACGCTTTTTGGCCCAGATACTCTCTATCTATAGAT T C PGGT1B Ensembl:ENSG00000164219 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs756304587 Functional Loss SNV dbSNP153 33..33 33 - - - 21468 RMVar_ID_21468 Human_SNP_ID_247239260 A-to-I Human chr5 - 115390382 115390382 115390382 AGACAATCAGCTGATAGCTGGCCAGAGTGTCCAGGCGATCATGGCTCAGCTTCCCTAGGAGCAAA AGACAATCAGCTGATAGCTGGCCAGAGTGTCCGGGCGATCATGGCTCAGCTTCCCTAGGAGCAAA T C CTNNA1P1 Ensembl:ENSG00000249026 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432832981 Functional Loss SNV dbSNP153 33..33 33 - - - 21469 RMVar_ID_21469 Human_SNP_ID_247239269 A-to-I Human chr5 - 115390410 115390410 115390410 TCAGAAGTAGGATGAGCATCCAGACAAAAGACAATCAGCTGATAGCTGGCCAGAGTGTCCAGGCG TCAGAAGTAGGATGAGCATCCAGACAAAAGACGATCAGCTGATAGCTGGCCAGAGTGTCCAGGCG T C CTNNA1P1 Ensembl:ENSG00000249026 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167995830 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1843194,Human_miRNA_ID_1880335,Human_miRNA_ID_1904337 21470 RMVar_ID_21470 Human_SNP_ID_247239337 A-to-I Human chr5 + 115390635 115390635 115390635 TTCCACAGCTGCTTCTGCTTGCTCAGTAAAACATGGCATGACTGTGTTGGAAAGCAGCTTAGTGG TTCCACAGCTGCTTCTGCTTGCTCAGTAAAACGTGGCATGACTGTGTTGGAAAGCAGCTTAGTGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879118692 Functional Loss SNV dbSNP153 33..33 33 - - - 21471 RMVar_ID_21471 Human_SNP_ID_247239343 A-to-I Human chr5 + 115390654 115390654 115390654 TGCTCAGTAAAACATGGCATGACTGTGTTGGAAAGCAGCTTAGTGGCTTCCAGAACCTTCTCTGT TGCTCAGTAAAACATGGCATGACTGTGTTGGAGAGCAGCTTAGTGGCTTCCAGAACCTTCTCTGT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs111866497 Functional Loss SNV dbSNP153 33..33 33 - - - 21472 RMVar_ID_21472 Human_SNP_ID_247239544 A-to-I Human chr5 - 115391299 115391299 115391299 ACATGGGCAATGCTGGATGTAAAGAAAGAAGTAATTCCCTCAATTCTGCTATAGATAAAATGACC ACATGGGCAATGCTGGATGTAAAGAAAGAAGTGATTCCCTCAATTCTGCTATAGATAAAATGACC T C CTNNA1P1 Ensembl:ENSG00000249026 Pseudogene exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs916914630 Functional Loss SNV dbSNP153 33..33 33 - - - 21473 RMVar_ID_21473 Human_SNP_ID_247239545 A-to-I Human chr5 - 115391299 115391299 115391299 ACATGGGCAATGCTGGATGTAAAGAAAGAAGTAATTCCCTCAATTCTGCTATAGATAAAATGACC ACATGGGCAATGCTGGATGTAAAGAAAGAAGTCATTCCCTCAATTCTGCTATAGATAAAATGACC T G CTNNA1P1 Ensembl:ENSG00000249026 Pseudogene exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs916914630 Functional Loss SNV dbSNP153 33..33 33 - - - 21474 RMVar_ID_21474 Human_SNP_ID_247239548 A-to-I Human chr5 + 115391314 115391314 115391314 AGCAGAATTGAGGGAATTACTTCTTTCTTTACATCCAGCATTGCCCATGTACTCCAAAAGCAGGT AGCAGAATTGAGGGAATTACTTCTTTCTTTACGTCCAGCATTGCCCATGTACTCCAAAAGCAGGT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1296047399 Functional Loss SNV dbSNP153 33..33 33 - - - 21475 RMVar_ID_21475 Human_SNP_ID_247239558 A-to-I Human chr5 + 115391337 115391337 115391337 TTTCTTTACATCCAGCATTGCCCATGTACTCCAAAAGCAGGTCCTGCAGGACCTGGAGGACAGTG TTTCTTTACATCCAGCATTGCCCATGTACTCCGAAAGCAGGTCCTGCAGGACCTGGAGGACAGTG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1171902622 Functional Loss SNV dbSNP153 33..33 33 - - - 21476 RMVar_ID_21476 Human_SNP_ID_247239735 A-to-I Human chr5 - 115391892 115391892 115391892 CAGCTGAAAGTTGTGGAAGATGATATCTTGAAATTGAGGAATGCTGGCAATGAACAAGACTTAGG CAGCTGAAAGTTGTGGAAGATGATATCTTGAAGTTGAGGAATGCTGGCAATGAACAAGACTTAGG T C CTNNA1P1 Ensembl:ENSG00000249026 Pseudogene exon GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1136423 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17416465 Human_miRNA_ID_1818616,Human_miRNA_ID_1859017,Human_miRNA_ID_1902889 21477 RMVar_ID_21477 Human_SNP_ID_247239738 A-to-I Human chr5 - 115391902 115391902 115391902 ATTACTTATTCAGCTGAAAGTTGTGGAAGATGATATCTTGAAATTGAGGAATGCTGGCAATGAAC ATTACTTATTCAGCTGAAAGTTGTGGAAGATGGTATCTTGAAATTGAGGAATGCTGGCAATGAAC T C CTNNA1P1 Ensembl:ENSG00000249026 Pseudogene exon GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1452313198 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17416465 Human_miRNA_ID_1828371,Human_miRNA_ID_1902889 21478 RMVar_ID_21478 Human_SNP_ID_247271156 A-to-I Human chr5 - 115508476 115508476 115508476 TAAAAATTAGCTGGGTATGGTGTCGCAAGCCTATAGTCCCACCTACACAGGAGGCTGAGGTGGGA TAAAAATTAGCTGGGTATGGTGTCGCAAGCCTGTAGTCCCACCTACACAGGAGGCTGAGGTGGGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs753663208 Functional Loss SNV dbSNP153 33..33 33 - - - 21479 RMVar_ID_21479 Human_SNP_ID_247272429 A-to-I Human chr5 - 115513266 115513266 115513266 TGACACACAAAGCATCGTGAAGGGATCGTTTCACCTCCTCAATGATCATCTTATTTCCTCCTCTG TGACACACAAAGCATCGTGAAGGGATCGTTTCGCCTCCTCAATGATCATCTTATTTCCTCCTCTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878921173 Functional Loss SNV dbSNP153 33..33 33 - - - 21480 RMVar_ID_21480 Human_SNP_ID_247274371 A-to-I Human chr5 - 115520958 115520958 115520958 CCAGCTAATAAATTGTCACACAATGGAAAATCATATGCCACAACATTCATTGTAAGGTTTAATAA CCAGCTAATAAATTGTCACACAATGGAAAATCGTATGCCACAACATTCATTGTAAGGTTTAATAA T C FEM1C Ensembl:ENSG00000145780 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs953056294 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7367678 Human_miRNA_ID_1205488,Human_miRNA_ID_2580703 RMVar_hsa_circ_89354,RMVar_hsa_circ_233877 21481 RMVar_ID_21481 Human_SNP_ID_247357654 A-to-I Human chr5 - 115829894 115829894 115829894 GCCAGGCTGGTCTCAAACTCCTGACTGACCTCAGGTGATCCACCCGCCTTGGCCTCCCAAAGTGC GCCAGGCTGGTCTCAAACTCCTGACTGACCTCGGGTGATCCACCCGCCTTGGCCTCCCAAAGTGC T C ATG12 Ensembl:ENSG00000145782 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs980495495 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27510733 21482 RMVar_ID_21482 Human_SNP_ID_247357890 A-to-I Human chr5 - 115830635 115830635 115830635 AGGCTGCAGAGGCAAGAGGATCCCCTGAGCCCAGAAGTTCAAGGGTATAGTGAGTCGTGATTGTA AGGCTGCAGAGGCAAGAGGATCCCCTGAGCCCGGAAGTTCAAGGGTATAGTGAGTCGTGATTGTA T C ATG12 Ensembl:ENSG00000145782 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1302593022 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_629377,Human_RBP_ID_5151298,Human_RBP_ID_15269711,Human_RBP_ID_26520110 21483 RMVar_ID_21483 Human_SNP_ID_247357938 A-to-I Human chr5 - 115830789 115830789 115830789 TTCCAGATCAGGCATGGTGGCTTACACCTGTAATCCCAGCACTTTGGAAGGCTGAGGTGTGGGGA TTCCAGATCAGGCATGGTGGCTTACACCTGTATTCCCAGCACTTTGGAAGGCTGAGGTGTGGGGA T A ATG12 Ensembl:ENSG00000145782 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs983458217 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_629381,Human_RBP_ID_15269722,Human_RBP_ID_22372093,Human_RBP_ID_26529201 Human_miRNA_ID_58487,Human_miRNA_ID_771898,Human_miRNA_ID_781606,Human_miRNA_ID_786462,Human_miRNA_ID_1600974,Human_miRNA_ID_1610419,Human_miRNA_ID_1615340,Human_miRNA_ID_1622829,Human_miRNA_ID_1638932 21484 RMVar_ID_21484 Human_SNP_ID_247357939 A-to-I Human chr5 - 115830789 115830789 115830789 TTCCAGATCAGGCATGGTGGCTTACACCTGTAATCCCAGCACTTTGGAAGGCTGAGGTGTGGGGA TTCCAGATCAGGCATGGTGGCTTACACCTGTAGTCCCAGCACTTTGGAAGGCTGAGGTGTGGGGA T C ATG12 Ensembl:ENSG00000145782 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs983458217 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_629381,Human_RBP_ID_15269722,Human_RBP_ID_22372093,Human_RBP_ID_26529201 Human_miRNA_ID_58487,Human_miRNA_ID_771898,Human_miRNA_ID_781606,Human_miRNA_ID_786462,Human_miRNA_ID_1600974,Human_miRNA_ID_1610419,Human_miRNA_ID_1615340,Human_miRNA_ID_1622829,Human_miRNA_ID_1638932 21485 RMVar_ID_21485 Human_SNP_ID_247360854 A-to-I Human chr5 - 115840325 115840325 115840325 CCATTGCACTCCAGCCTGGACAACAAGAGCGAAACTCCGCCTCAAAAAAAAAAAAAAAAAAGACA CCATTGCACTCCAGCCTGGACAACAAGAGCGACACTCCGCCTCAAAAAAAAAAAAAAAAAAGACA T G ATG12 Ensembl:ENSG00000145782 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1305571630 Functional Loss SNV dbSNP153 33..33 33 - - - 21486 RMVar_ID_21486 Human_SNP_ID_247420465 A-to-I Human chr5 - 116052275 116052275 116052275 GCTGCTACTCTCCGAGCTTCGCAATGCCGCCCAAGGACGACGAGAAGAAGGACGCTGGAAAGTCA GCTGCTACTCTCCGAGCTTCGCAATGCCGCCCGAGGACGACGAGAAGAAGGACGCTGGAAAGTCA T C AC034236.1 Ensembl:ENSG00000185641 Pseudogene exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1447220844 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_629443,Human_RBP_ID_4848341,Human_RBP_ID_8600055,Human_RBP_ID_26530395,Human_RBP_ID_27072848 21487 RMVar_ID_21487 Human_SNP_ID_247455980 A-to-I Human chr5 + 116164083 116164083 116164083 TCACGTCTGTAATCCCAGCATTTTGGGAAGCTAAGGAGGGCGGATCACCTGACGTCAGGAGTTCT TCACGTCTGTAATCCCAGCATTTTGGGAAGCTGAGGAGGGCGGATCACCTGACGTCAGGAGTTCT A G COMMD10 Ensembl:ENSG00000145781 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs367955670 Functional Loss SNV dbSNP153 33..33 33 - - - 21488 RMVar_ID_21488 Human_SNP_ID_247470571 A-to-I Human chr5 + 116207709 116207709 116207709 CACCACACCCAGCTAATTTCTGTGTTTTTAGTAGAGATGAGGTTTCACCACGTTGGCCAGGCTAG CACCACACCCAGCTAATTTCTGTGTTTTTAGTGGAGATGAGGTTTCACCACGTTGGCCAGGCTAG A G COMMD10 Ensembl:ENSG00000145781 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1228096806 Functional Loss SNV dbSNP153 33..33 33 - - - 21489 RMVar_ID_21489 Human_SNP_ID_247512985 A-to-I Human chr5 + 116336408 116336408 116336408 CAGCTGCTACAATGAGTGGCTAAAAATACTCTAGACGTTTTTCTCTCCCCATTCCACAGTTTGTA CAGCTGCTACAATGAGTGGCTAAAAATACTCTGGACGTTTTTCTCTCCCCATTCCACAGTTTGTA A G COMMD10 Ensembl:ENSG00000145781 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1385570536 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36055 21490 RMVar_ID_21490 Human_SNP_ID_248237962 A-to-I Human chr5 - 118837775 118837775 118837775 AGCTAGAACCTCAGCCCCATGCCACCACACTCAGCTAATTTTAAATTTTACTAATTTCATTTAAT AGCTAGAACCTCAGCCCCATGCCACCACACTCTGCTAATTTTAAATTTTACTAATTTCATTTAAT T A DTWD2 Ensembl:ENSG00000169570 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1307533617 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8600211 21491 RMVar_ID_21491 Human_SNP_ID_248237963 A-to-I Human chr5 - 118837779 118837779 118837779 AAGTAGCTAGAACCTCAGCCCCATGCCACCACACTCAGCTAATTTTAAATTTTACTAATTTCATT AAGTAGCTAGAACCTCAGCCCCATGCCACCACGCTCAGCTAATTTTAAATTTTACTAATTTCATT T C DTWD2 Ensembl:ENSG00000169570 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs572923437 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8600211 21492 RMVar_ID_21492 Human_SNP_ID_248237975 A-to-I Human chr5 - 118837836 118837836 118837836 TAGCTTACTGCAGCATCAAACTCCTGGGCTCAAGTGTTCCTCCTGCCTCAGCCTCCCAAGTAGCT TAGCTTACTGCAGCATCAAACTCCTGGGCTCAGGTGTTCCTCCTGCCTCAGCCTCCCAAGTAGCT T C DTWD2 Ensembl:ENSG00000169570 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1027343315 Functional Loss SNV dbSNP153 33..33 33 - - - 21493 RMVar_ID_21493 Human_SNP_ID_248237976 A-to-I Human chr5 - 118837837 118837837 118837837 ATAGCTTACTGCAGCATCAAACTCCTGGGCTCAAGTGTTCCTCCTGCCTCAGCCTCCCAAGTAGC ATAGCTTACTGCAGCATCAAACTCCTGGGCTCGAGTGTTCCTCCTGCCTCAGCCTCCCAAGTAGC T C DTWD2 Ensembl:ENSG00000169570 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1354101532 Functional Loss SNV dbSNP153 33..33 33 - - - 21494 RMVar_ID_21494 Human_SNP_ID_248238279 A-to-I Human chr5 - 118839062 118839062 118839062 TGCCTCCTGGGTTCACGCCATTCTTCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGTGCCCA TGCCTCCTGGGTTCACGCCATTCTTCTGCCTCGGCCTCCTGAGTAGCTGGGACTACAGGTGCCCA T C DTWD2 Ensembl:ENSG00000169570 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1376736919 Functional Loss SNV dbSNP153 33..33 33 - - - 21495 RMVar_ID_21495 Human_SNP_ID_248238312 A-to-I Human chr5 - 118839160 118839160 118839160 TTAGTCATTATTATTATTATTATTATTATTTGAGATGGAATCTCGCTCTGTCGCCCAGGCTGGAG TTAGTCATTATTATTATTATTATTATTATTTGCGATGGAATCTCGCTCTGTCGCCCAGGCTGGAG T G DTWD2 Ensembl:ENSG00000169570 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1207231061 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7370229 21496 RMVar_ID_21496 Human_SNP_ID_248238382 A-to-I Human chr5 - 118839430 118839430 118839430 GGATCGCTGGAGCCCAGGACATCAAGGTTGCAAGGAGCTATGTTCATTCCACTGCACTCCAGCCT GGATCGCTGGAGCCCAGGACATCAAGGTTGCAGGGAGCTATGTTCATTCCACTGCACTCCAGCCT T C DTWD2 Ensembl:ENSG00000169570 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1254691747 Functional Loss SNV dbSNP153 33..33 33 - - - 21497 RMVar_ID_21497 Human_SNP_ID_248238401 A-to-I Human chr5 - 118839493 118839493 118839493 ATAATTAGCCAGATGTGGTGGTGTGCACTTGTAGTCCTAGCTACTTGGGAGGCTAAGGTGGGAGG ATAATTAGCCAGATGTGGTGGTGTGCACTTGTGGTCCTAGCTACTTGGGAGGCTAAGGTGGGAGG T C DTWD2 Ensembl:ENSG00000169570 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1189491572 Functional Loss SNV dbSNP153 33..33 33 - - - 21498 RMVar_ID_21498 Human_SNP_ID_248238411 A-to-I Human chr5 - 118839515 118839515 118839515 TCCATACAAAATTAAAAAAAAAATAATTAGCCAGATGTGGTGGTGTGCACTTGTAGTCCTAGCTA TCCATACAAAATTAAAAAAAAAATAATTAGCCCGATGTGGTGGTGTGCACTTGTAGTCCTAGCTA T G DTWD2 Ensembl:ENSG00000169570 Protein coding 3'UTR GSE100210;GSE99789 HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 29129909,29796672 RNA-Seq:(High) rs1048252503 Functional Loss SNV dbSNP153 33..33 33 - - - 21499 RMVar_ID_21499 Human_SNP_ID_248307397 A-to-I Human chr5 + 119078194 119078194 119078194 TAAAGATGAGGTCTTGCTGTGTTGCCAGGGCTAGTCTGGAACTTCTGGCCTCAAGTGATCCTACT TAAAGATGAGGTCTTGCTGTGTTGCCAGGGCTCGTCTGGAACTTCTGGCCTCAAGTGATCCTACT A C DMXL1 Ensembl:ENSG00000172869 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909276873 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93745,RMVar_hsa_circ_233916,RMVar_hsa_circ_317746 21500 RMVar_ID_21500 Human_SNP_ID_248307398 A-to-I Human chr5 + 119078194 119078194 119078194 TAAAGATGAGGTCTTGCTGTGTTGCCAGGGCTAGTCTGGAACTTCTGGCCTCAAGTGATCCTACT TAAAGATGAGGTCTTGCTGTGTTGCCAGGGCTGGTCTGGAACTTCTGGCCTCAAGTGATCCTACT A G DMXL1 Ensembl:ENSG00000172869 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909276873 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93745,RMVar_hsa_circ_233916,RMVar_hsa_circ_317746 21501 RMVar_ID_21501 Human_SNP_ID_248313991 A-to-I Human chr5 + 119099880 119099880 119099880 GTAAATAGCCGGACATGGTAGTATGCTCCTGTAGTCCTAGCTACCCGGGAAGCTGAGGCGGGAGA GTAAATAGCCGGACATGGTAGTATGCTCCTGTGGTCCTAGCTACCCGGGAAGCTGAGGCGGGAGA A G DMXL1 Ensembl:ENSG00000172869 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1318565464 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15273082 RMVar_hsa_circ_20836,RMVar_hsa_circ_93745,RMVar_hsa_circ_283706,RMVar_hsa_circ_233917,RMVar_hsa_circ_233916,RMVar_hsa_circ_317746,RMVar_hsa_circ_359089,RMVar_hsa_circ_367735,RMVar_hsa_circ_300955,RMVar_hsa_circ_271850,RMVar_hsa_circ_274183,RMVar_hsa_circ_29844,RMVar_hsa_circ_233919,RMVar_hsa_circ_233921,RMVar_hsa_circ_233922,RMVar_hsa_circ_233923,RMVar_hsa_circ_233920,RMVar_hsa_circ_233918 21502 RMVar_ID_21502 Human_SNP_ID_248323319 A-to-I Human chr5 - 119126924 119126924 119126924 CAAAAACTGAAGGACTCTGAAACTGAGCTCCAACGGTGCCAAGAGCAAAAAGGAATTTAAGCACA CAAAAACTGAAGGACTCTGAAACTGAGCTCCATCGGTGCCAAGAGCAAAAAGGAATTTAAGCACA T A AC118465.1 Ensembl:ENSG00000248885 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs950826763 Functional Loss SNV dbSNP153 33..33 33 - - - 21503 RMVar_ID_21503 Human_SNP_ID_248377538 A-to-I Human chr5 + 119319231 119319231 119319231 AGGAGTTCAAGGCTGCAGTGAGCTGTGATGGCACTACTACACTTCAGCCTGGGCAATGAAGTGAG AGGAGTTCAAGGCTGCAGTGAGCTGTGATGGCTCTACTACACTTCAGCCTGGGCAATGAAGTGAG A T TNFAIP8 Ensembl:ENSG00000145779 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs757291097 Functional Loss SNV dbSNP153 33..33 33 - - - 21504 RMVar_ID_21504 Human_SNP_ID_248380225 A-to-I Human chr5 + 119329786 119329786 119329786 CACACTGTGGACATCTCCAGGTGCTTAGCAGCAGGATTTCCCCAGCCTTGTCTAGACATGGACCA CACACTGTGGACATCTCCAGGTGCTTAGCAGCGGGATTTCCCCAGCCTTGTCTAGACATGGACCA A G TNFAIP8 Ensembl:ENSG00000145779 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1044577077 Functional Loss SNV dbSNP153 33..33 33 - - - 21505 RMVar_ID_21505 Human_SNP_ID_248393292 A-to-I Human chr5 + 119379670 119379670 119379670 TGGAGTGGAGTGGCGTGATCTGAGTTCACTGCAGCCTCAACCTCCCAGGCTTGAGCAATCCTCCC TGGAGTGGAGTGGCGTGATCTGAGTTCACTGCCGCCTCAACCTCCCAGGCTTGAGCAATCCTCCC A C TNFAIP8 Ensembl:ENSG00000145779 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1478131577 Functional Loss SNV dbSNP153 33..33 33 - - - 21506 RMVar_ID_21506 Human_SNP_ID_248396490 A-to-I Human chr5 + 119391674 119391674 119391674 CCAGCTACTCTGGAGACTGAGTTGTGAGAATCACTTGAACCCGGGAGGTGGAGGTTGCAGTGAGC CCAGCTACTCTGGAGACTGAGTTGTGAGAATCGCTTGAACCCGGGAGGTGGAGGTTGCAGTGAGC A G TNFAIP8 Ensembl:ENSG00000145779 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049750354 Functional Loss SNV dbSNP153 33..33 33 - - - 21507 RMVar_ID_21507 Human_SNP_ID_248397965 A-to-I Human chr5 + 119396831 119396831 119396831 CCTGGCCAACGTGGTGAAACCCCACTGCTACTAAAAATACACAAGATTAGCCAGATGTGGTGGCA CCTGGCCAACGTGGTGAAACCCCACTGCTACTGAAAATACACAAGATTAGCCAGATGTGGTGGCA A G TNFAIP8 Ensembl:ENSG00000145779 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs936112645 Functional Loss SNV dbSNP153 33..33 33 - - - 21508 RMVar_ID_21508 Human_SNP_ID_248423784 A-to-I Human chr5 + 119488762 119488762 119488762 CTACCCTGGTGGTCTAGTGGTTAGGATTCAGCACTCTCAATCATTATTTGCCACTGTAATGGTCT CTACCCTGGTGGTCTAGTGGTTAGGATTCAGCGCTCTCAATCATTATTTGCCACTGTAATGGTCT A G HSD17B4 Ensembl:ENSG00000133835 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1406980439 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87060,RMVar_hsa_circ_73028,RMVar_hsa_circ_113419,RMVar_hsa_circ_233980,RMVar_hsa_circ_357201,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_58377,RMVar_hsa_circ_75060,RMVar_hsa_circ_53834,RMVar_hsa_circ_233983 21509 RMVar_ID_21509 Human_SNP_ID_671106774 A-to-I Human chr20 - 312703 312703 312703 CTCTACAAAAAAAAAAATTGAAAATTAAAATTAGCTGAGTGTGGTGGCACACACCTGTGGTCCTA CTCTACAAAAAAAAAAATTGAAAATTAAAATTGGCTGAGTGTGGTGGCACACACCTGTGGTCCTA T C NRSN2-AS1,NRSN2-AS1:2,NRSN2-AS1:3,NRSN2-AS1:4,NRSN2-AS1:5,NRSN2-AS1:6 RNACentral:URS0000D5B425,RNACentral:URS0000D5C6C5,RNACentral:URS0000D5B23F,RNACentral:URS0000D5D5D7,RNACentral:URS0000D5D3F8,RNACentral:URS0000D58AA2 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1413250703 Functional Loss SNV dbSNP153 33..33 33 - - - 21510 RMVar_ID_21510 Human_SNP_ID_671107336 A-to-I Human chr20 - 315173 315172 315174 AAACAAACAAACAAAAAAAGCCAGTGGCTCATACCTATAATCCCAGCACTTTGGGAGGCTAGCTT AAACAAACAAACAAAAAAAGCCAGTGGCTCA__CCTATAATCCCAGCACTTTGGGAGGCTAGCTT GTA G NRSN2-AS1,NRSN2-AS1:2,NRSN2-AS1:3,NRSN2-AS1:4,NRSN2-AS1:5 RNACentral:URS0000D5B425,RNACentral:URS0000D5C6C5,RNACentral:URS0000D5B23F,RNACentral:URS0000D5D5D7,RNACentral:URS0000D5D3F8 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1395342168 Functional Loss DEL dbSNP153 32..33 33 - - - 21511 RMVar_ID_21511 Human_SNP_ID_671107337 A-to-I Human chr20 - 315173 315173 315173 AAACAAACAAACAAAAAAAGCCAGTGGCTCATACCTATAATCCCAGCACTTTGGGAGGCTAGCTT AAACAAACAAACAAAAAAAGCCAGTGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCTAGCTT T C NRSN2-AS1,NRSN2-AS1:2,NRSN2-AS1:3,NRSN2-AS1:4,NRSN2-AS1:5 RNACentral:URS0000D5B425,RNACentral:URS0000D5C6C5,RNACentral:URS0000D5B23F,RNACentral:URS0000D5D5D7,RNACentral:URS0000D5D3F8 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1165583056 Functional Loss SNV dbSNP153 33..33 33 - - - 21512 RMVar_ID_21512 Human_SNP_ID_671107589 A-to-I Human chr20 - 316065 316065 316065 TGATCACACCACTGCACTCCAGCCTGGGTGACAGAGTGGAACTGTCTCAAAGAAAAAAATATATA TGATCACACCACTGCACTCCAGCCTGGGTGACTGAGTGGAACTGTCTCAAAGAAAAAAATATATA T A NRSN2-AS1,NRSN2-AS1:2,NRSN2-AS1:3,NRSN2-AS1:4,NRSN2-AS1:5 RNACentral:URS0000D5B425,RNACentral:URS0000D5C6C5,RNACentral:URS0000D5B23F,RNACentral:URS0000D5D5D7,RNACentral:URS0000D5D3F8 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs964618840 Functional Loss SNV dbSNP153 33..33 33 - - - 21513 RMVar_ID_21513 Human_SNP_ID_671107823 A-to-I Human chr20 - 317192 317192 317192 TCCCTCACTTTATGCTTGTGTGGGTTTTTTTTAGAGACCTGGTCTTGCTCTGTTGCCTGGGCTGG TCCCTCACTTTATGCTTGTGTGGGTTTTTTTTGGAGACCTGGTCTTGCTCTGTTGCCTGGGCTGG T C NRSN2-AS1 Ensembl:ENSG00000225377 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs931722798 Functional Loss SNV dbSNP153 33..33 33 - - - 21514 RMVar_ID_21514 Human_SNP_ID_671108729 A-to-I Human chr20 - 320054 320054 320054 ACGGGGTTTCACTATGTTGGCCGGCTGATCTCAAACTCTTGACCCCGTGATCCGCCCGCATCAGC ACGGGGTTTCACTATGTTGGCCGGCTGATCTCGAACTCTTGACCCCGTGATCCGCCCGCATCAGC T C NRSN2-AS1 Ensembl:ENSG00000225377 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886859678 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14057758 21515 RMVar_ID_21515 Human_SNP_ID_671108765 A-to-I Human chr20 - 320204 320204 320204 TTGCCCAGGCTGAAGGGCAGTGGCACGATCTCAGCTCACCACAACCTCTGCCTCCCGGGTTCAAG TTGCCCAGGCTGAAGGGCAGTGGCACGATCTCGGCTCACCACAACCTCTGCCTCCCGGGTTCAAG T C NRSN2-AS1 Ensembl:ENSG00000225377 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1183270598 Functional Loss SNV dbSNP153 33..33 33 - - - 21516 RMVar_ID_21516 Human_SNP_ID_671113784 A-to-I Human chr20 - 336932 336932 336932 ACAGAGGGCTGGGCACAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGATGCTGGCGG ACAGAGGGCTGGGCACAGTGGCTCATGCCTGTTATCCCAGCACTTTGGGAGGCTGATGCTGGCGG T A NRSN2-AS1 Ensembl:ENSG00000225377 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1317713813 Functional Loss SNV dbSNP153 33..33 33 - - - 21517 RMVar_ID_21517 Human_SNP_ID_671134929 A-to-I Human chr20 + 414229 414229 414229 GAACTCGAGTTTAAGACCAGCCTGGGCAACATAGTGAGACCTTGTCTCTGCAAAAAATAAAAAAA GAACTCGAGTTTAAGACCAGCCTGGGCAACATGGTGAGACCTTGTCTCTGCAAAAAATAAAAAAA A G RBCK1 Ensembl:ENSG00000125826 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1285223877 Functional Loss SNV dbSNP153 33..33 33 - - - 21518 RMVar_ID_21518 Human_SNP_ID_671144869 A-to-I Human chr20 - 449582 449582 449582 TTCACTTATCATTTTTTTTGAGACGGAGTCTCACTTTGTCGCCCAGGCTGGAGTGCAGTGGCACG TTCACTTATCATTTTTTTTGAGACGGAGTCTCGCTTTGTCGCCCAGGCTGGAGTGCAGTGGCACG T C TBC1D20 Ensembl:ENSG00000125875 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1327698313 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108702,RMVar_hsa_circ_208254,RMVar_hsa_circ_208260,RMVar_hsa_circ_125269,RMVar_hsa_circ_208258 21519 RMVar_ID_21519 Human_SNP_ID_671145572 A-to-I Human chr20 - 452565 452565 452565 TCACCTAGGCTGAAGTGCAGTGGTGCTATCATAGCTCACCACAGCCTTATACTCCTGGGCTCAAG TCACCTAGGCTGAAGTGCAGTGGTGCTATCATTGCTCACCACAGCCTTATACTCCTGGGCTCAAG T A TBC1D20 Ensembl:ENSG00000125875 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1197581239 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108702,RMVar_hsa_circ_208254,RMVar_hsa_circ_208260,RMVar_hsa_circ_125269,RMVar_hsa_circ_208258 21520 RMVar_ID_21520 Human_SNP_ID_671151682 A-to-I Human chr20 - 475348 475348 475348 TCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGTTGGGATTATAGGCACATGCCACCACACCCA TCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTGGTTGGGATTATAGGCACATGCCACCACACCCA T C CSNK2A1 Ensembl:ENSG00000101266 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs760630813 Functional Loss SNV dbSNP153 33..33 33 - - - 21521 RMVar_ID_21521 Human_SNP_ID_671151960 A-to-I Human chr20 - 476337 476337 476337 GGAGAATTGCTTGAGCCTGGGAGGTGGCGGTTACAGTGAGCTGAGATCACGTCAGTGTACTCCAG GGAGAATTGCTTGAGCCTGGGAGGTGGCGGTTTCAGTGAGCTGAGATCACGTCAGTGTACTCCAG T A CSNK2A1 Ensembl:ENSG00000101266 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1307018942 Functional Loss SNV dbSNP153 33..33 33 - - - 21522 RMVar_ID_21522 Human_SNP_ID_671151997 A-to-I Human chr20 - 476487 476487 476487 GGGAGACCAAGGCGAGTGGATCACCTGAGGTCAGGAGTTTGAAACCAGACTGAACAACATGGTGA GGGAGACCAAGGCGAGTGGATCACCTGAGGTCCGGAGTTTGAAACCAGACTGAACAACATGGTGA T G CSNK2A1 Ensembl:ENSG00000101266 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1296321962 Functional Loss SNV dbSNP153 33..33 33 - - - 21523 RMVar_ID_21523 Human_SNP_ID_671152126 A-to-I Human chr20 - 477088 477087 477089 GGCCACGAGTTGGAGACCAGCCTGGGCAACATAGGGAGACCCTGTCTCTACCAAAATTAAAAATT GGCCACGAGTTGGAGACCAGCCTGGGCAACA__GGGAGACCCTGTCTCTACCAAAATTAAAAATT CTA C CSNK2A1 Ensembl:ENSG00000101266 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005222219 Functional Loss DEL dbSNP153 32..33 33 - - - 21524 RMVar_ID_21524 Human_SNP_ID_671154208 A-to-I Human chr20 - 485005 485005 485005 CTGGAGTGCAGTGGCACAATCTCAGCTGCTGCAGCCTCCGCCTCCCGGGTTCAAGCGATTCTCCC CTGGAGTGCAGTGGCACAATCTCAGCTGCTGCGGCCTCCGCCTCCCGGGTTCAAGCGATTCTCCC T C CSNK2A1 Ensembl:ENSG00000101266 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1275424922 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7007531 RMVar_hsa_circ_87023,RMVar_hsa_circ_118003,RMVar_hsa_circ_105940,RMVar_hsa_circ_208262,RMVar_hsa_circ_78590,RMVar_hsa_circ_82604,RMVar_hsa_circ_208264,RMVar_hsa_circ_208265,RMVar_hsa_circ_208263,RMVar_hsa_circ_208261 21525 RMVar_ID_21525 Human_SNP_ID_671155667 A-to-I Human chr20 - 490234 490234 490234 TCATGAGGTCAGGAGTTTGAGACCACTGGCCAACGTAGTGAAACCCCGTCTCTACTAAAAATACA TCATGAGGTCAGGAGTTTGAGACCACTGGCCAGCGTAGTGAAACCCCGTCTCTACTAAAAATACA T C CSNK2A1 Ensembl:ENSG00000101266 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1295970272 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29190,RMVar_hsa_circ_118003,RMVar_hsa_circ_105940,RMVar_hsa_circ_208262,RMVar_hsa_circ_78590,RMVar_hsa_circ_82604,RMVar_hsa_circ_208264,RMVar_hsa_circ_208265,RMVar_hsa_circ_208263,RMVar_hsa_circ_208268,RMVar_hsa_circ_310206,RMVar_hsa_circ_345796,RMVar_hsa_circ_4492,RMVar_hsa_circ_208267,RMVar_hsa_circ_121316,RMVar_hsa_circ_208270 21526 RMVar_ID_21526 Human_SNP_ID_671156085 A-to-I Human chr20 - 491632 491632 491632 GGGTTTTGCTCTGTTGCCCAGGCTGGAGTGCAATGCCATGATCATAGCTGACTGCAGCCCCGAAC GGGTTTTGCTCTGTTGCCCAGGCTGGAGTGCAGTGCCATGATCATAGCTGACTGCAGCCCCGAAC T C CSNK2A1 Ensembl:ENSG00000101266 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1439156474 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14124862 RMVar_hsa_circ_29190,RMVar_hsa_circ_118003,RMVar_hsa_circ_105940,RMVar_hsa_circ_208262,RMVar_hsa_circ_78590,RMVar_hsa_circ_82604,RMVar_hsa_circ_208264,RMVar_hsa_circ_208265,RMVar_hsa_circ_208263,RMVar_hsa_circ_208268,RMVar_hsa_circ_310206,RMVar_hsa_circ_345796,RMVar_hsa_circ_4492,RMVar_hsa_circ_208267,RMVar_hsa_circ_121316,RMVar_hsa_circ_208270 21527 RMVar_ID_21527 Human_SNP_ID_671161189 A-to-I Human chr20 - 510848 510848 510848 GCCAGCTGTGGTAGCCCACGCCTGTGGTCCCAACTACTTGGGAGGCAGAGGTGGGAGGATTGATT GCCAGCTGTGGTAGCCCACGCCTGTGGTCCCAGCTACTTGGGAGGCAGAGGTGGGAGGATTGATT T C CSNK2A1 Ensembl:ENSG00000101266 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1209225210 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118003,RMVar_hsa_circ_78590,RMVar_hsa_circ_208264,RMVar_hsa_circ_208265,RMVar_hsa_circ_31242,RMVar_hsa_circ_51193,RMVar_hsa_circ_71880,RMVar_hsa_circ_307797,RMVar_hsa_circ_208278 21528 RMVar_ID_21528 Human_SNP_ID_671162022 A-to-I Human chr20 - 514189 514189 514189 CAGTTGTACTCCACTACACCCAGCTCATTTTTATGTTATTTGTAGAGAGGAGGTCTCGCTGTGTT CAGTTGTACTCCACTACACCCAGCTCATTTTTGTGTTATTTGTAGAGAGGAGGTCTCGCTGTGTT T C CSNK2A1 Ensembl:ENSG00000101266 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1263856159 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118003,RMVar_hsa_circ_78590,RMVar_hsa_circ_208264,RMVar_hsa_circ_208265,RMVar_hsa_circ_31242,RMVar_hsa_circ_51193,RMVar_hsa_circ_71880,RMVar_hsa_circ_307797,RMVar_hsa_circ_208278 21529 RMVar_ID_21529 Human_SNP_ID_671166523 A-to-I Human chr20 - 530612 530612 530612 AAAATTAACTGGGCGTGGTGGCGCACACCCATAGTCCCAGCTACTTGGAAGACTGAGGTAGGAGG AAAATTAACTGGGCGTGGTGGCGCACACCCATGGTCCCAGCTACTTGGAAGACTGAGGTAGGAGG T C CSNK2A1 Ensembl:ENSG00000101266 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs540450586 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571319 RMVar_hsa_circ_118003,RMVar_hsa_circ_208265 21530 RMVar_ID_21530 Human_SNP_ID_671166524 A-to-I Human chr20 - 530612 530612 530612 AAAATTAACTGGGCGTGGTGGCGCACACCCATAGTCCCAGCTACTTGGAAGACTGAGGTAGGAGG AAAATTAACTGGGCGTGGTGGCGCACACCCATCGTCCCAGCTACTTGGAAGACTGAGGTAGGAGG T G CSNK2A1 Ensembl:ENSG00000101266 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs540450586 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571319 RMVar_hsa_circ_118003,RMVar_hsa_circ_208265 21531 RMVar_ID_21531 Human_SNP_ID_671166525 A-to-I Human chr20 - 530614 530614 530614 AGAAAATTAACTGGGCGTGGTGGCGCACACCCATAGTCCCAGCTACTTGGAAGACTGAGGTAGGA AGAAAATTAACTGGGCGTGGTGGCGCACACCCGTAGTCCCAGCTACTTGGAAGACTGAGGTAGGA T C CSNK2A1 Ensembl:ENSG00000101266 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs745856414 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571319 RMVar_hsa_circ_118003,RMVar_hsa_circ_208265 21532 RMVar_ID_21532 Human_SNP_ID_671322011 A-to-I Human chr20 + 1144960 1144960 1144960 CAGTGTGGAGTGCAGTGGTGCGATCTCGGCTCACTGCAGCCTCCGCCTCCCGGGTTCAAGCAACT CAGTGTGGAGTGCAGTGGTGCGATCTCGGCTCGCTGCAGCCTCCGCCTCCCGGGTTCAAGCAACT A G PSMF1 Ensembl:ENSG00000125818 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1431870558 Functional Loss SNV dbSNP153 33..33 33 - - - 21533 RMVar_ID_21533 Human_SNP_ID_671327232 A-to-I Human chr20 + 1166914 1166914 1166914 AGGATGATAGAGACCATCAGATAGAAGCAGGGAAGGTAGATAACTTTTAGGACCTTGATGTGAGG AGGATGATAGAGACCATCAGATAGAAGCAGGGGAGGTAGATAACTTTTAGGACCTTGATGTGAGG A G PSMF1 Ensembl:ENSG00000125818 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202198990 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1024776,Human_RBP_ID_14032374 RMVar_hsa_circ_55856 21534 RMVar_ID_21534 Human_SNP_ID_671327733 A-to-I Human chr20 + 1169116 1169116 1169116 TGCTCTCTGGACCGTAACCTTTTTGGTTACAAAAGGTAAATTTCTGTTTACTGCATCTGAACCCC TGCTCTCTGGACCGTAACCTTTTTGGTTACAAGAGGTAAATTTCTGTTTACTGCATCTGAACCCC A G PSMF1 Ensembl:ENSG00000125818 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs953502267 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55856 21535 RMVar_ID_21535 Human_SNP_ID_671327833 A-to-I Human chr20 + 1169568 1169568 1169568 CTGACGCATTAGTCCTGGGATTCAGCTGCAGTAAACAGAAATTTACCTTTTGTAACCAAAAAGGT CTGACGCATTAGTCCTGGGATTCAGCTGCAGTTAACAGAAATTTACCTTTTGTAACCAAAAAGGT A T PSMF1 Ensembl:ENSG00000125818 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1267483383 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55856 21536 RMVar_ID_21536 Human_SNP_ID_671327836 A-to-I Human chr20 + 1169580 1169580 1169580 TCCTGGGATTCAGCTGCAGTAAACAGAAATTTACCTTTTGTAACCAAAAAGGTAATGGTCCAGAG TCCTGGGATTCAGCTGCAGTAAACAGAAATTTGCCTTTTGTAACCAAAAAGGTAATGGTCCAGAG A G PSMF1 Ensembl:ENSG00000125818 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285772477 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55856 21537 RMVar_ID_21537 Human_SNP_ID_671327838 A-to-I Human chr20 + 1169601 1169601 1169601 AACAGAAATTTACCTTTTGTAACCAAAAAGGTAATGGTCCAGAGAGCAGCAGGATCACATCATCA AACAGAAATTTACCTTTTGTAACCAAAAAGGTTATGGTCCAGAGAGCAGCAGGATCACATCATCA A T PSMF1 Ensembl:ENSG00000125818 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048066140 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55856 21538 RMVar_ID_21538 Human_SNP_ID_671327843 A-to-I Human chr20 + 1169630 1169630 1169630 GGTAATGGTCCAGAGAGCAGCAGGATCACATCATCATTGCTACAATCTGGGGATTAGGAACTCCA GGTAATGGTCCAGAGAGCAGCAGGATCACATCGTCATTGCTACAATCTGGGGATTAGGAACTCCA A G PSMF1 Ensembl:ENSG00000125818 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs907407310 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22722838 RMVar_hsa_circ_55856 21539 RMVar_ID_21539 Human_SNP_ID_671327845 A-to-I Human chr20 + 1169639 1169639 1169639 CCAGAGAGCAGCAGGATCACATCATCATTGCTACAATCTGGGGATTAGGAACTCCAGAGCCACAC CCAGAGAGCAGCAGGATCACATCATCATTGCTGCAATCTGGGGATTAGGAACTCCAGAGCCACAC A G PSMF1 Ensembl:ENSG00000125818 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs141863026 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22722838 RMVar_hsa_circ_55856 21540 RMVar_ID_21540 Human_SNP_ID_671327852 A-to-I Human chr20 + 1169683 1169683 1169683 TTAGGAACTCCAGAGCCACACAGCAGCTGCCTATATCTGCACCAAAAAGTAGATGTCCTTCACAC TTAGGAACTCCAGAGCCACACAGCAGCTGCCTGTATCTGCACCAAAAAGTAGATGTCCTTCACAC A G PSMF1 Ensembl:ENSG00000125818 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs967342088 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55856 21541 RMVar_ID_21541 Human_SNP_ID_671367948 A-to-I Human chr20 + 1336222 1336222 1336222 ATGAGAAAGAATCTCCCATGAGATCAGGGGCTAGCTCATTAATCTAGGTGAGTATGCCATTTTGG ATGAGAAAGAATCTCCCATGAGATCAGGGGCTGGCTCATTAATCTAGGTGAGTATGCCATTTTGG A G SDCBP2-AS1 Ensembl:ENSG00000234684 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1385224691 Functional Loss SNV dbSNP153 33..33 33 - - - 21542 RMVar_ID_21542 Human_SNP_ID_671367963 A-to-I Human chr20 + 1336259 1336259 1336259 ATTAATCTAGGTGAGTATGCCATTTTGGAGATAGACAAACTGAGCCCTGGAGAGGTCAAATGACT ATTAATCTAGGTGAGTATGCCATTTTGGAGATGGACAAACTGAGCCCTGGAGAGGTCAAATGACT A G SDCBP2-AS1 Ensembl:ENSG00000234684 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs768658040 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5249625 21543 RMVar_ID_21543 Human_SNP_ID_671368788 A-to-I Human chr20 + 1339488 1339488 1339488 TGCCACCACACCCTGATAATTTTTGTATTTTTAGTAGAGATGATGTTTCTCCATGTTGCTCAGGC TGCCACCACACCCTGATAATTTTTGTATTTTTTGTAGAGATGATGTTTCTCCATGTTGCTCAGGC A T SDCBP2-AS1 Ensembl:ENSG00000234684 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1471068456 Functional Loss SNV dbSNP153 33..33 33 - - - 21544 RMVar_ID_21544 Human_SNP_ID_671368790 A-to-I Human chr20 + 1339508 1339508 1339508 TTTTGTATTTTTAGTAGAGATGATGTTTCTCCATGTTGCTCAGGCTGGTCTTGAACTCAAGCAAT TTTTGTATTTTTAGTAGAGATGATGTTTCTCCGTGTTGCTCAGGCTGGTCTTGAACTCAAGCAAT A G SDCBP2-AS1 Ensembl:ENSG00000234684 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1421635106 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14034642 21545 RMVar_ID_21545 Human_SNP_ID_671371271 A-to-I Human chr20 + 1350418 1350418 1350418 ATGGCTCACTGTGACCTCCGCCTCCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGG ATGGCTCACTGTGACCTCCGCCTCCCAGGTTCCAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGG A C SDCBP2-AS1 Ensembl:ENSG00000234684 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1369842431 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2054106,Human_Splice_Rec_2054107,Human_Splice_Rec_2054124,Human_Splice_Rec_2054125 21546 RMVar_ID_21546 Human_SNP_ID_671502098 A-to-I Human chr20 + 1902498 1902498 1902498 ATTCATTCAACAAATATTTTTGAGCACCTACTATGTGCCAGGGATGGCTCTAGGTGCTTGGAGGA ATTCATTCAACAAATATTTTTGAGCACCTACTGTGTGCCAGGGATGGCTCTAGGTGCTTGGAGGA A G SIRPA Ensembl:ENSG00000198053 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs989090551 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10262 21547 RMVar_ID_21547 Human_SNP_ID_671557482 A-to-I Human chr20 + 2118929 2118929 2118929 TGTGTAGTAGGCTACACCATCTAGGTTTATGTAAGTACACTCTTGACATTACACAACAATCGCCT TGTGTAGTAGGCTACACCATCTAGGTTTATGTGAGTACACTCTTGACATTACACAACAATCGCCT A G STK35 Ensembl:ENSG00000125834 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1568576597 Functional Loss SNV dbSNP153 33..33 33 - - - 21548 RMVar_ID_21548 Human_SNP_ID_671560460 A-to-I Human chr20 + 2131149 2131149 2131149 ATGGAGTGTTCTTACACAGTCCTGGATGGTATAGCCTCCTATACACCTAGGTTATATGGTAGATA ATGGAGTGTTCTTACACAGTCCTGGATGGTATGGCCTCCTATACACCTAGGTTATATGGTAGATA A G STK35 Ensembl:ENSG00000125834 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1311868675 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571323 21549 RMVar_ID_21549 Human_SNP_ID_671560482 A-to-I Human chr20 + 2131212 2131212 2131212 TAGAGCCTATTGCTCCTAGACTGCAAACCTGTACAGCATGTTGTGGTACTGAATACTACTATAGG TAGAGCCTATTGCTCCTAGACTGCAAACCTGTGCAGCATGTTGTGGTACTGAATACTACTATAGG A G STK35 Ensembl:ENSG00000125834 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs887276721 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571324 21550 RMVar_ID_21550 Human_SNP_ID_671648163 A-to-I Human chr20 - 2475808 2475805 2475808 TTGCCCAGGCTGGAGTGCAATGGCACGATCTCAGCTCACGGCAACATCCACCTCCCTGGTTCAAG TTGCCCAGGCTGGAGTGCAATGGCACGATCTC___TCACGGCAACATCCACCTCCCTGGTTCAAG AGCT A AL049650.2 Ensembl:ENSG00000256566 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1296033677 Functional Loss DEL dbSNP153 33..35 33 - - - 21551 RMVar_ID_21551 Human_SNP_ID_671650772 A-to-I Human chr20 - 2486735 2486735 2486735 TAAGATGGAGTTTCGCTCTTGTTGCCCAGGCTAGAGTGCAATCGTGCAATCTCGGCTCACCACAA TAAGATGGAGTTTCGCTCTTGTTGCCCAGGCTGGAGTGCAATCGTGCAATCTCGGCTCACCACAA T C ZNF343,AL049650.2 Ensembl:ENSG00000088876,Ensembl:ENSG00000256566 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs939171744 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2054972 RMVar_hsa_circ_208305 21552 RMVar_ID_21552 Human_SNP_ID_671694593 A-to-I Human chr20 - 2660294 2660294 2660294 AGTTGCTGAACTGTACCCCAAAATCAAATTTGAGACAATGATCATAGACAACTGCTGCATGCAGG AGTTGCTGAACTGTACCCCAAAATCAAATTTGGGACAATGATCATAGACAACTGCTGCATGCAGG T C IDH3B Ensembl:ENSG00000101365 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs372393324 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_560718,Human_RBP_ID_1025164,Human_RBP_ID_1594255,Human_RBP_ID_1927282,Human_RBP_ID_8260325,Human_RBP_ID_8853181,Human_RBP_ID_9115995,Human_RBP_ID_9388523,Human_RBP_ID_14056200,Human_RBP_ID_18770064,Human_RBP_ID_23005552 Human_Splice_Rec_2055265,Human_Splice_Rec_2055275,Human_Splice_Rec_2055294,Human_Splice_Rec_2055295,Human_Splice_Rec_2055316,Human_Splice_Rec_2055317,Human_Splice_Rec_2055338,Human_Splice_Rec_2055339,Human_Splice_Rec_2055360,Human_Splice_Rec_2055361,Human_Splice_Rec_2055369,Human_Splice_Rec_2055390,Human_Splice_Rec_2055391,Human_Splice_Rec_2055401 RMVar_hsa_circ_88903,RMVar_hsa_circ_105929,RMVar_hsa_circ_100427,RMVar_hsa_circ_90389,RMVar_hsa_circ_92565,RMVar_hsa_circ_74951,RMVar_hsa_circ_208326,RMVar_hsa_circ_208330,RMVar_hsa_circ_83240,RMVar_hsa_circ_208328,RMVar_hsa_circ_208329,RMVar_hsa_circ_208327,RMVar_hsa_circ_208325,RMVar_hsa_circ_85686,RMVar_hsa_circ_96242,RMVar_hsa_circ_208336,RMVar_hsa_circ_63077,RMVar_hsa_circ_208335 21553 RMVar_ID_21553 Human_SNP_ID_671740471 A-to-I Human chr20 - 2834728 2834728 2834728 AGCTGTGACTACAGGCGCACACCACCACACCTAGCTAGTTTTTGTATTTTTAGTAGAGAAGAGAT AGCTGTGACTACAGGCGCACACCACCACACCTGGCTAGTTTTTGTATTTTTAGTAGAGAAGAGAT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1453251823 Functional Loss SNV dbSNP153 33..33 33 - - - 21554 RMVar_ID_21554 Human_SNP_ID_671749837 A-to-I Human chr20 + 2866101 2866101 2866101 GGGGTTGGGGGATTATATGTACTGACGGGTGTATACATATAGAATATATATGGACGATGTATGCA GGGGTTGGGGGATTATATGTACTGACGGGTGTGTACATATAGAATATATATGGACGATGTATGCA A G VPS16,PTPRA Ensembl:ENSG00000215305,Ensembl:ENSG00000132670 Protein coding,Protein coding intron,intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs538676218 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23898397 RMVar_hsa_circ_106822,RMVar_hsa_circ_80268,RMVar_hsa_circ_208353,RMVar_hsa_circ_208358,RMVar_hsa_circ_121559,RMVar_hsa_circ_78201,RMVar_hsa_circ_97409,RMVar_hsa_circ_208361,RMVar_hsa_circ_95057,RMVar_hsa_circ_208363,RMVar_hsa_circ_208364,RMVar_hsa_circ_125467,RMVar_hsa_circ_208365,RMVar_hsa_circ_208366 21555 RMVar_ID_21555 Human_SNP_ID_671753920 A-to-I Human chr20 + 2882402 2882402 2882402 GCATTGACCTCCCAGTCTCAAGTGATCATCCTACCTCAGCCTCTCAAGTAGCCAGGACCACAGGC GCATTGACCTCCCAGTCTCAAGTGATCATCCTCCCTCAGCCTCTCAAGTAGCCAGGACCACAGGC A C PTPRA Ensembl:ENSG00000132670 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560594447 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125467,RMVar_hsa_circ_208366 21556 RMVar_ID_21556 Human_SNP_ID_671753921 A-to-I Human chr20 + 2882402 2882402 2882402 GCATTGACCTCCCAGTCTCAAGTGATCATCCTACCTCAGCCTCTCAAGTAGCCAGGACCACAGGC GCATTGACCTCCCAGTCTCAAGTGATCATCCTGCCTCAGCCTCTCAAGTAGCCAGGACCACAGGC A G PTPRA Ensembl:ENSG00000132670 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560594447 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125467,RMVar_hsa_circ_208366 21557 RMVar_ID_21557 Human_SNP_ID_671753922 A-to-I Human chr20 + 2882402 2882402 2882402 GCATTGACCTCCCAGTCTCAAGTGATCATCCTACCTCAGCCTCTCAAGTAGCCAGGACCACAGGC GCATTGACCTCCCAGTCTCAAGTGATCATCCTTCCTCAGCCTCTCAAGTAGCCAGGACCACAGGC A T PTPRA Ensembl:ENSG00000132670 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560594447 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125467,RMVar_hsa_circ_208366 21558 RMVar_ID_21558 Human_SNP_ID_671758455 A-to-I Human chr20 + 2900806 2900806 2900806 TTGAACTCAGGAGGCATAGGTTGCAGTGACCCAAGATCAAGCCATTGCACTCCAGCCTGAGCAAC TTGAACTCAGGAGGCATAGGTTGCAGTGACCCGAGATCAAGCCATTGCACTCCAGCCTGAGCAAC A G PTPRA Ensembl:ENSG00000132670 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1333922346 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_208368,RMVar_hsa_circ_125467,RMVar_hsa_circ_208366,RMVar_hsa_circ_208367 21559 RMVar_ID_21559 Human_SNP_ID_671765660 A-to-I Human chr20 + 2928369 2928369 2928369 GTGTTAGCTGATCTGCCCTCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGTAC GTGTTAGCTGATCTGCCCTCCTTGGCCTCCCAGAGTGCTGGGATTACAGGCGTGAGCCACCGTAC A G PTPRA Ensembl:ENSG00000132670 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1282412624 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_368014,RMVar_hsa_circ_304089,RMVar_hsa_circ_331833,RMVar_hsa_circ_280049,RMVar_hsa_circ_208372,RMVar_hsa_circ_65322,RMVar_hsa_circ_208371 21560 RMVar_ID_21560 Human_SNP_ID_671766444 A-to-I Human chr20 + 2931763 2931763 2931763 TGTGTGTGTGTGTGTGTAAGAGACTGGGTCTCATTCTGTTACCCAGGCATGAGTGCCATGGCATA TGTGTGTGTGTGTGTGTAAGAGACTGGGTCTCCTTCTGTTACCCAGGCATGAGTGCCATGGCATA A C PTPRA Ensembl:ENSG00000132670 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1246561322 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5652257,Human_RBP_ID_23898468 RMVar_hsa_circ_72082,RMVar_hsa_circ_125467,RMVar_hsa_circ_208366,RMVar_hsa_circ_340487,RMVar_hsa_circ_208367,RMVar_hsa_circ_368014,RMVar_hsa_circ_304089,RMVar_hsa_circ_331833,RMVar_hsa_circ_280049,RMVar_hsa_circ_208372,RMVar_hsa_circ_65322,RMVar_hsa_circ_208371 21561 RMVar_ID_21561 Human_SNP_ID_671777484 A-to-I Human chr20 + 2977570 2977570 2977570 GGGACGCTGAGGTGGGAGGATCACCTGAGCCCAGGAAATGGAGGTTGCAGTGAGCCAAGATTGCG GGGACGCTGAGGTGGGAGGATCACCTGAGCCCGGGAAATGGAGGTTGCAGTGAGCCAAGATTGCG A G PTPRA Ensembl:ENSG00000132670 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1362320209 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23078,RMVar_hsa_circ_72082,RMVar_hsa_circ_125467,RMVar_hsa_circ_208366,RMVar_hsa_circ_331833,RMVar_hsa_circ_65322,RMVar_hsa_circ_325596,RMVar_hsa_circ_332747,RMVar_hsa_circ_79818,RMVar_hsa_circ_300408,RMVar_hsa_circ_116201,RMVar_hsa_circ_62589,RMVar_hsa_circ_66766,RMVar_hsa_circ_30041,RMVar_hsa_circ_46593,RMVar_hsa_circ_208376,RMVar_hsa_circ_208377,RMVar_hsa_circ_208378,RMVar_hsa_circ_70250,RMVar_hsa_circ_300451,RMVar_hsa_circ_208379 21562 RMVar_ID_21562 Human_SNP_ID_671778128 A-to-I Human chr20 + 2980386 2980386 2980386 GGTCAGGAGTTCAAGACCAGGCTGGCCAACATAGTGAAACCCTGTCTCTACTAAAAATACAAAAC GGTCAGGAGTTCAAGACCAGGCTGGCCAACATGGTGAAACCCTGTCTCTACTAAAAATACAAAAC A G PTPRA Ensembl:ENSG00000132670 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs200832158 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23078,RMVar_hsa_circ_72082,RMVar_hsa_circ_125467,RMVar_hsa_circ_208366,RMVar_hsa_circ_331833,RMVar_hsa_circ_65322,RMVar_hsa_circ_325596,RMVar_hsa_circ_332747,RMVar_hsa_circ_79818,RMVar_hsa_circ_300408,RMVar_hsa_circ_116201,RMVar_hsa_circ_62589,RMVar_hsa_circ_66766,RMVar_hsa_circ_30041,RMVar_hsa_circ_46593,RMVar_hsa_circ_208376,RMVar_hsa_circ_208377,RMVar_hsa_circ_208378,RMVar_hsa_circ_70250,RMVar_hsa_circ_300451,RMVar_hsa_circ_208379 21563 RMVar_ID_21563 Human_SNP_ID_671778131 A-to-I Human chr20 + 2980406 2980406 2980406 GCTGGCCAACATAGTGAAACCCTGTCTCTACTAAAAATACAAAACTTAGCCAGGCCTGCAGTTCC GCTGGCCAACATAGTGAAACCCTGTCTCTACTGAAAATACAAAACTTAGCCAGGCCTGCAGTTCC A G PTPRA Ensembl:ENSG00000132670 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs951314310 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23078,RMVar_hsa_circ_72082,RMVar_hsa_circ_125467,RMVar_hsa_circ_208366,RMVar_hsa_circ_331833,RMVar_hsa_circ_65322,RMVar_hsa_circ_325596,RMVar_hsa_circ_332747,RMVar_hsa_circ_79818,RMVar_hsa_circ_300408,RMVar_hsa_circ_116201,RMVar_hsa_circ_62589,RMVar_hsa_circ_66766,RMVar_hsa_circ_30041,RMVar_hsa_circ_46593,RMVar_hsa_circ_208376,RMVar_hsa_circ_208377,RMVar_hsa_circ_208378,RMVar_hsa_circ_70250,RMVar_hsa_circ_300451,RMVar_hsa_circ_208379 21564 RMVar_ID_21564 Human_SNP_ID_671784096 A-to-I Human chr20 + 3005287 3005287 3005287 GAGTGCGTTCATGGCAGTACTCAGTGGCTCATACCTGTAATCCCAGAACTTTGGAAGGCCAAGGT GAGTGCGTTCATGGCAGTACTCAGTGGCTCATGCCTGTAATCCCAGAACTTTGGAAGGCCAAGGT A G PTPRA Ensembl:ENSG00000132670 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1223910727 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23078,RMVar_hsa_circ_125467,RMVar_hsa_circ_208366,RMVar_hsa_circ_65322,RMVar_hsa_circ_332747,RMVar_hsa_circ_116201,RMVar_hsa_circ_66766,RMVar_hsa_circ_30041,RMVar_hsa_circ_208378,RMVar_hsa_circ_70250,RMVar_hsa_circ_208382,RMVar_hsa_circ_374403,RMVar_hsa_circ_287517,RMVar_hsa_circ_40208,RMVar_hsa_circ_123954,RMVar_hsa_circ_208380,RMVar_hsa_circ_208381,RMVar_hsa_circ_326859,RMVar_hsa_circ_338930,RMVar_hsa_circ_18763,RMVar_hsa_circ_114884,RMVar_hsa_circ_61693,RMVar_hsa_circ_342244,RMVar_hsa_circ_321375,RMVar_hsa_circ_208388,RMVar_hsa_circ_208389 21565 RMVar_ID_21565 Human_SNP_ID_671784350 A-to-I Human chr20 + 3006304 3006304 3006304 GAATTCCTGGGCTCAAGTAATCCTCCTGCCACAGCCTGCTGAGTAACTAGAACTACAGGTGCATC GAATTCCTGGGCTCAAGTAATCCTCCTGCCACTGCCTGCTGAGTAACTAGAACTACAGGTGCATC A T PTPRA Ensembl:ENSG00000132670 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs367797953 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23078,RMVar_hsa_circ_125467,RMVar_hsa_circ_208366,RMVar_hsa_circ_65322,RMVar_hsa_circ_332747,RMVar_hsa_circ_116201,RMVar_hsa_circ_66766,RMVar_hsa_circ_30041,RMVar_hsa_circ_208378,RMVar_hsa_circ_70250,RMVar_hsa_circ_208382,RMVar_hsa_circ_374403,RMVar_hsa_circ_287517,RMVar_hsa_circ_40208,RMVar_hsa_circ_123954,RMVar_hsa_circ_208380,RMVar_hsa_circ_208381,RMVar_hsa_circ_326859,RMVar_hsa_circ_338930,RMVar_hsa_circ_18763,RMVar_hsa_circ_114884,RMVar_hsa_circ_61693,RMVar_hsa_circ_342244,RMVar_hsa_circ_321375,RMVar_hsa_circ_208388,RMVar_hsa_circ_208389 21566 RMVar_ID_21566 Human_SNP_ID_671785232 A-to-I Human chr20 + 3009910 3009910 3009910 TCACCCCGACACCCAGGCTGGATTGCACTGGTACGATCTTGGCTTACTACGACCTCTGCCTCCCG TCACCCCGACACCCAGGCTGGATTGCACTGGTGCGATCTTGGCTTACTACGACCTCTGCCTCCCG A G PTPRA Ensembl:ENSG00000132670 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1377215936 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23078,RMVar_hsa_circ_125467,RMVar_hsa_circ_208366,RMVar_hsa_circ_116201,RMVar_hsa_circ_66766,RMVar_hsa_circ_30041,RMVar_hsa_circ_208378,RMVar_hsa_circ_374403,RMVar_hsa_circ_40208,RMVar_hsa_circ_123954,RMVar_hsa_circ_208380,RMVar_hsa_circ_208381,RMVar_hsa_circ_326859,RMVar_hsa_circ_18763,RMVar_hsa_circ_114884,RMVar_hsa_circ_61693,RMVar_hsa_circ_342244,RMVar_hsa_circ_1790,RMVar_hsa_circ_208389,RMVar_hsa_circ_26929 21567 RMVar_ID_21567 Human_SNP_ID_671785237 A-to-I Human chr20 + 3009926 3009926 3009926 GCTGGATTGCACTGGTACGATCTTGGCTTACTACGACCTCTGCCTCCCGGGCTCAAGCGATTCTC GCTGGATTGCACTGGTACGATCTTGGCTTACTGCGACCTCTGCCTCCCGGGCTCAAGCGATTCTC A G PTPRA Ensembl:ENSG00000132670 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1441736718 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23078,RMVar_hsa_circ_125467,RMVar_hsa_circ_208366,RMVar_hsa_circ_116201,RMVar_hsa_circ_66766,RMVar_hsa_circ_30041,RMVar_hsa_circ_208378,RMVar_hsa_circ_374403,RMVar_hsa_circ_40208,RMVar_hsa_circ_123954,RMVar_hsa_circ_208380,RMVar_hsa_circ_208381,RMVar_hsa_circ_326859,RMVar_hsa_circ_18763,RMVar_hsa_circ_114884,RMVar_hsa_circ_61693,RMVar_hsa_circ_342244,RMVar_hsa_circ_1790,RMVar_hsa_circ_208389,RMVar_hsa_circ_26929 21568 RMVar_ID_21568 Human_SNP_ID_671785261 A-to-I Human chr20 + 3010033 3010033 3010033 ACCATGCCCAGCTAATTTTTTGTATTTTTAGTAGAGACGGTGTTTTGCTATGCTGGCCAGGCTGG ACCATGCCCAGCTAATTTTTTGTATTTTTAGTGGAGACGGTGTTTTGCTATGCTGGCCAGGCTGG A G PTPRA Ensembl:ENSG00000132670 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1278568917 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23078,RMVar_hsa_circ_125467,RMVar_hsa_circ_208366,RMVar_hsa_circ_116201,RMVar_hsa_circ_66766,RMVar_hsa_circ_30041,RMVar_hsa_circ_208378,RMVar_hsa_circ_374403,RMVar_hsa_circ_40208,RMVar_hsa_circ_123954,RMVar_hsa_circ_208380,RMVar_hsa_circ_208381,RMVar_hsa_circ_326859,RMVar_hsa_circ_18763,RMVar_hsa_circ_114884,RMVar_hsa_circ_61693,RMVar_hsa_circ_342244,RMVar_hsa_circ_1790,RMVar_hsa_circ_208389,RMVar_hsa_circ_26929 21569 RMVar_ID_21569 Human_SNP_ID_671786334 A-to-I Human chr20 + 3014550 3014550 3014550 CTTGTGATCCCAGCTCCTTGGGAAGCTGAGGCAGGAGAATCACTTGAACCCGGGAGCAGAAGGTT CTTGTGATCCCAGCTCCTTGGGAAGCTGAGGCGGGAGAATCACTTGAACCCGGGAGCAGAAGGTT A G PTPRA Ensembl:ENSG00000132670 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs752109243 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571336 RMVar_hsa_circ_23078,RMVar_hsa_circ_125467,RMVar_hsa_circ_208366,RMVar_hsa_circ_116201,RMVar_hsa_circ_66766,RMVar_hsa_circ_30041,RMVar_hsa_circ_208378,RMVar_hsa_circ_374403,RMVar_hsa_circ_40208,RMVar_hsa_circ_123954,RMVar_hsa_circ_208380,RMVar_hsa_circ_208381,RMVar_hsa_circ_326859,RMVar_hsa_circ_18763,RMVar_hsa_circ_114884,RMVar_hsa_circ_61693,RMVar_hsa_circ_342244,RMVar_hsa_circ_1790,RMVar_hsa_circ_208389,RMVar_hsa_circ_26929 21570 RMVar_ID_21570 Human_SNP_ID_671787996 A-to-I Human chr20 + 3020164 3020164 3020164 GGAGTCTCGCTCTGTCGCCCAGGCTGAAGGGCAGTGGTGCCATCTCGGCTCACTGCAAGCTCCGC GGAGTCTCGCTCTGTCGCCCAGGCTGAAGGGCTGTGGTGCCATCTCGGCTCACTGCAAGCTCCGC A T PTPRA Ensembl:ENSG00000132670 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1348187913 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125467,RMVar_hsa_circ_208366,RMVar_hsa_circ_116201,RMVar_hsa_circ_66766,RMVar_hsa_circ_208378,RMVar_hsa_circ_123954,RMVar_hsa_circ_208380,RMVar_hsa_circ_326859,RMVar_hsa_circ_114884,RMVar_hsa_circ_61693,RMVar_hsa_circ_208389,RMVar_hsa_circ_56901 21571 RMVar_ID_21571 Human_SNP_ID_671789512 A-to-I Human chr20 + 3026138 3026138 3026138 CGGCTAATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCATGCGGGTCTCAAACTCCTAACCT CGGCTAATTTTTAGTAGAGACAGGGTTTCACCGTGTTGGCCATGCGGGTCTCAAACTCCTAACCT A G PTPRA Ensembl:ENSG00000132670 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1265027244 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125467,RMVar_hsa_circ_208366,RMVar_hsa_circ_66766,RMVar_hsa_circ_43987,RMVar_hsa_circ_114884,RMVar_hsa_circ_61693,RMVar_hsa_circ_208389 21572 RMVar_ID_21572 Human_SNP_ID_671798946 A-to-I Human chr20 - 3060225 3060225 3060225 TGCCTGTAATCCCAGGAGGCAGAGGTTGCAGTAAGCCAAGATCGCACCATTGCACTCCAGCTTGG TGCCTGTAATCCCAGGAGGCAGAGGTTGCAGTGAGCCAAGATCGCACCATTGCACTCCAGCTTGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1020905455 Functional Loss SNV dbSNP153 33..33 33 - - - 21573 RMVar_ID_21573 Human_SNP_ID_671812541 A-to-I Human chr20 - 3108245 3108245 3108245 AAATTAGCTGGGCATGGTGGTGTGTGCCTGTAATGCCAGCTACTCAGGAGGCTGAGGCATGAGAA AAATTAGCTGGGCATGGTGGTGTGTGCCTGTATTGCCAGCTACTCAGGAGGCTGAGGCATGAGAA T A UBOX5 Ensembl:ENSG00000185019 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1215902855 Functional Loss SNV dbSNP153 33..33 33 - - - 21574 RMVar_ID_21574 Human_SNP_ID_671812667 A-to-I Human chr20 - 3108811 3108811 3108811 CTTCTACCTCAGCCTCCCAGGTAGCAGGAACTATAGGCATGTGCCACCATGCCCAGCTAATTTTT CTTCTACCTCAGCCTCCCAGGTAGCAGGAACTGTAGGCATGTGCCACCATGCCCAGCTAATTTTT T C UBOX5 Ensembl:ENSG00000185019 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1277426252 Functional Loss SNV dbSNP153 33..33 33 - - - 21575 RMVar_ID_21575 Human_SNP_ID_671815319 A-to-I Human chr20 - 3118817 3118817 3118817 CTCATGCCTCAGCCTCTGGAATAGCTGGGACTATAGGTGCGTGCCAACACGCCTGGCTGATTTTT CTCATGCCTCAGCCTCTGGAATAGCTGGGACTGTAGGTGCGTGCCAACACGCCTGGCTGATTTTT T C UBOX5 Ensembl:ENSG00000185019 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1314877504 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75957,RMVar_hsa_circ_208394 21576 RMVar_ID_21576 Human_SNP_ID_671821980 A-to-I Human chr20 - 3143234 3143234 3143234 GCCAGATGTGGTGGCACACACCTTAGCAACTCAGGAGGCTGAAGCATGAGAATCACTTGAGCCTA GCCAGATGTGGTGGCACACACCTTAGCAACTCCGGAGGCTGAAGCATGAGAATCACTTGAGCCTA T G UBOX5 Ensembl:ENSG00000185019 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1326916675 Functional Loss SNV dbSNP153 33..33 33 - - - 21577 RMVar_ID_21577 Human_SNP_ID_671833120 A-to-I Human chr20 - 3184817 3184817 3184817 TATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGGTCTTGATCTCCTGACCTCATGA TATTTTTAGTAGAGACGGGGTTTCACCGTGTTGGCCAGGATGGTCTTGATCTCCTGACCTCATGA T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1165031343 Functional Loss SNV dbSNP153 33..33 33 - - - 21578 RMVar_ID_21578 Human_SNP_ID_671834154 A-to-I Human chr20 - 3188660 3188660 3188660 GTGATCTCGGCTTACTACAACCTCCACCACCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCG GTGATCTCGGCTTACTACAACCTCCACCACCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCG T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1384972775 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14068895 21579 RMVar_ID_21579 Human_SNP_ID_671834159 A-to-I Human chr20 - 3188676 3188676 3188676 TGTTGCCCAGGCTGTAGTGATCTCGGCTTACTACAACCTCCACCACCCAGGTTCAAGCGATTCTC TGTTGCCCAGGCTGTAGTGATCTCGGCTTACTGCAACCTCCACCACCCAGGTTCAAGCGATTCTC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1568497785 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14068895 21580 RMVar_ID_21580 Human_SNP_ID_671840220 A-to-I Human chr20 - 3208532 3208532 3208532 ATCTCTACCAAAAAGTACAAAATTAGCTGGGCATGGTGGTGCATGCCTGTAATCCCAGTTCAGAG ATCTCTACCAAAAAGTACAAAATTAGCTGGGCGTGGTGGTGCATGCCTGTAATCCCAGTTCAGAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1218312377 Functional Loss SNV dbSNP153 33..33 33 - - - 21581 RMVar_ID_21581 Human_SNP_ID_671840819 A-to-I Human chr20 + 3210912 3210912 3210912 ATCTCTACTAAAAATACAAAAATTAACTGGGCATGGTGACACGTGCCTGTAGTCCCAGCTACTCG ATCTCTACTAAAAATACAAAAATTAACTGGGCGTGGTGACACGTGCCTGTAGTCCCAGCTACTCG A G ITPA Ensembl:ENSG00000125877 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1038456822 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_208399,RMVar_hsa_circ_106937 21582 RMVar_ID_21582 Human_SNP_ID_671840958 A-to-I Human chr20 + 3211295 3211289 3211296 TCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTATCTGGGATTGCAGGCATGTATCACCACGCCTG TCAAGCAATTCTCCTGCCTCAGCCTCC_______CTGGGATTGCAGGCATGTATCACCACGCCTG CCGAGTAT C ITPA Ensembl:ENSG00000125877 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1378066962 Functional Loss DEL dbSNP153 28..34 33 - - - RMVar_hsa_circ_208399,RMVar_hsa_circ_106937 21583 RMVar_ID_21583 Human_SNP_ID_671840980 A-to-I Human chr20 + 3211349 3211349 3211349 CACCACGCCTGGTTAATTTTTGTATTTTTAGTAGAAACGGGATTTCGTCATGTTGGCCAGACTGG CACCACGCCTGGTTAATTTTTGTATTTTTAGTGGAAACGGGATTTCGTCATGTTGGCCAGACTGG A G ITPA Ensembl:ENSG00000125877 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1388172662 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_208399,RMVar_hsa_circ_106937 21584 RMVar_ID_21584 Human_SNP_ID_671841097 A-to-I Human chr20 + 3211766 3211766 3211766 CCGCCCGCCAGGGCCTCCCGAAGTGTTAGATTACATGCGTGAGCCACCGTGCCTGGCCGAACGGG CCGCCCGCCAGGGCCTCCCGAAGTGTTAGATTGCATGCGTGAGCCACCGTGCCTGGCCGAACGGG A G ITPA Ensembl:ENSG00000125877 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs529664164 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_208399,RMVar_hsa_circ_106937 21585 RMVar_ID_21585 Human_SNP_ID_671841249 A-to-I Human chr20 + 3212376 3212376 3212376 GAGTCTCACTCTGTCGCCTAAGGCTGGAGTGCAATGGTGCAATCTTGGCTCACTGTAGCCTCAAC GAGTCTCACTCTGTCGCCTAAGGCTGGAGTGCCATGGTGCAATCTTGGCTCACTGTAGCCTCAAC A C ITPA Ensembl:ENSG00000125877 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1390836275 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14173616 RMVar_hsa_circ_208399,RMVar_hsa_circ_106937 21586 RMVar_ID_21586 Human_SNP_ID_671843327 A-to-I Human chr20 + 3219347 3219347 3219347 ATGTTAATTCTTGGCCAGGTTTGGTGATTTACACCTGTAATCCTAGCACTTTGCGAGGCCCCAGC ATGTTAATTCTTGGCCAGGTTTGGTGATTTACGCCTGTAATCCTAGCACTTTGCGAGGCCCCAGC A G ITPA Ensembl:ENSG00000125877 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs763892733 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22479044 RMVar_hsa_circ_208399,RMVar_hsa_circ_106937,RMVar_hsa_circ_78223,RMVar_hsa_circ_208400,RMVar_hsa_circ_208401,RMVar_hsa_circ_95783,RMVar_hsa_circ_22999,RMVar_hsa_circ_87549,RMVar_hsa_circ_208406 21587 RMVar_ID_21587 Human_SNP_ID_671843461 A-to-I Human chr20 + 3219837 3219837 3219837 GTGAAGCAAAGGCAGGAGGATTGCTTGAGGCCAGGAGTTTGAGACCAGCCTGGGTAACATAGCCA GTGAAGCAAAGGCAGGAGGATTGCTTGAGGCCGGGAGTTTGAGACCAGCCTGGGTAACATAGCCA A G ITPA Ensembl:ENSG00000125877 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1181866698 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25602164 RMVar_hsa_circ_208399,RMVar_hsa_circ_106937,RMVar_hsa_circ_78223,RMVar_hsa_circ_208400,RMVar_hsa_circ_208401,RMVar_hsa_circ_95783,RMVar_hsa_circ_22999,RMVar_hsa_circ_87549,RMVar_hsa_circ_208406 21588 RMVar_ID_21588 Human_SNP_ID_671843806 A-to-I Human chr20 + 3221126 3221126 3221126 GTGGCTCAGGCTGGTCTCAATTTCCTGGGCTCAAGTGATCTTCCCACCTCAGCCTCCCAAAGTCC GTGGCTCAGGCTGGTCTCAATTTCCTGGGCTCCAGTGATCTTCCCACCTCAGCCTCCCAAAGTCC A C ITPA Ensembl:ENSG00000125877 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1302498120 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_208399,RMVar_hsa_circ_106937,RMVar_hsa_circ_78223,RMVar_hsa_circ_208400,RMVar_hsa_circ_208401,RMVar_hsa_circ_95783,RMVar_hsa_circ_22999,RMVar_hsa_circ_87549,RMVar_hsa_circ_208406 21589 RMVar_ID_21589 Human_SNP_ID_671857804 A-to-I Human chr20 - 3268578 3268578 3268578 TCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGCAGATCACGAAGTCAGGAGTTCGAG TCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGCAGATCACGAAGTCAGGAGTTCGAG T C C20orf194 Ensembl:ENSG00000088854 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1186305443 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35431,RMVar_hsa_circ_14188,RMVar_hsa_circ_14141,RMVar_hsa_circ_10209,RMVar_hsa_circ_208413,RMVar_hsa_circ_98391,RMVar_hsa_circ_325351,RMVar_hsa_circ_354067,RMVar_hsa_circ_208414,RMVar_hsa_circ_336893,RMVar_hsa_circ_43132 21590 RMVar_ID_21590 Human_SNP_ID_671860292 A-to-I Human chr20 - 3278678 3278678 3278678 GTCTTACTCTGTCGCCCAGATTGGAGTGCAATAGCGTGGTCTCGGCTCACTGCAACCTCTGCCTC GTCTTACTCTGTCGCCCAGATTGGAGTGCAATGGCGTGGTCTCGGCTCACTGCAACCTCTGCCTC T C C20orf194 Ensembl:ENSG00000088854 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1225284726 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35431,RMVar_hsa_circ_14188,RMVar_hsa_circ_10209,RMVar_hsa_circ_208413,RMVar_hsa_circ_98391,RMVar_hsa_circ_325351,RMVar_hsa_circ_208414,RMVar_hsa_circ_336893,RMVar_hsa_circ_43132,RMVar_hsa_circ_208415,RMVar_hsa_circ_8916,RMVar_hsa_circ_275533,RMVar_hsa_circ_362455,RMVar_hsa_circ_362993,RMVar_hsa_circ_38395,RMVar_hsa_circ_208416 21591 RMVar_ID_21591 Human_SNP_ID_671864687 A-to-I Human chr20 - 3295773 3295773 3295773 ACTGAATATTGAAGCTGCAGAACATCATTTGCAGGACAAGGAGGACTTCCAGAATAAAGTGGACA ACTGAATATTGAAGCTGCAGAACATCATTTGCGGGACAAGGAGGACTTCCAGAATAAAGTGGACA T C C20orf194 Ensembl:ENSG00000088854 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879194491 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14075171 RMVar_hsa_circ_7379,RMVar_hsa_circ_10209,RMVar_hsa_circ_336893,RMVar_hsa_circ_8916,RMVar_hsa_circ_38395,RMVar_hsa_circ_280352,RMVar_hsa_circ_50634,RMVar_hsa_circ_12905,RMVar_hsa_circ_20089,RMVar_hsa_circ_347147,RMVar_hsa_circ_16214,RMVar_hsa_circ_286355,RMVar_hsa_circ_12726,RMVar_hsa_circ_346113,RMVar_hsa_circ_307886,RMVar_hsa_circ_10943,RMVar_hsa_circ_10873 21592 RMVar_ID_21592 Human_SNP_ID_671878088 A-to-I Human chr20 - 3347778 3347778 3347778 AGCTGGGATTACTGGCACACACCACCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGTT AGCTGGGATTACTGGCACACACCACCATGCCCGGCTAATTTTTGTATTTTTAGTAGAGATGGGTT T C C20orf194 Ensembl:ENSG00000088854 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs545859482 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92694,RMVar_hsa_circ_208432,RMVar_hsa_circ_43213,RMVar_hsa_circ_18157,RMVar_hsa_circ_63181,RMVar_hsa_circ_127380,RMVar_hsa_circ_208442,RMVar_hsa_circ_31423,RMVar_hsa_circ_208445,RMVar_hsa_circ_32128,RMVar_hsa_circ_308906,RMVar_hsa_circ_104008,RMVar_hsa_circ_208444,RMVar_hsa_circ_278393,RMVar_hsa_circ_47609,RMVar_hsa_circ_54018,RMVar_hsa_circ_305716,RMVar_hsa_circ_208446,RMVar_hsa_circ_6680 21593 RMVar_ID_21593 Human_SNP_ID_671878124 A-to-I Human chr20 - 3347908 3347908 3347908 TGTTACGCATTTTACCTTTGAAATGGAGTCTCACTCTGTCGCCCAGGCTGGAGTGCAGTGGCATG TGTTACGCATTTTACCTTTGAAATGGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCATG T C C20orf194 Ensembl:ENSG00000088854 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1376812678 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92694,RMVar_hsa_circ_208432,RMVar_hsa_circ_43213,RMVar_hsa_circ_18157,RMVar_hsa_circ_63181,RMVar_hsa_circ_127380,RMVar_hsa_circ_208442,RMVar_hsa_circ_31423,RMVar_hsa_circ_208445,RMVar_hsa_circ_32128,RMVar_hsa_circ_308906,RMVar_hsa_circ_104008,RMVar_hsa_circ_208444,RMVar_hsa_circ_278393,RMVar_hsa_circ_47609,RMVar_hsa_circ_54018,RMVar_hsa_circ_305716,RMVar_hsa_circ_208446,RMVar_hsa_circ_6680 21594 RMVar_ID_21594 Human_SNP_ID_671880809 A-to-I Human chr20 - 3357910 3357910 3357910 GAACTCCTGAGCTCAAGTGATTCTTGCACCTCAGCCTCCTGAGTAGCTGGGACTACAGGCGTGCA GAACTCCTGAGCTCAAGTGATTCTTGCACCTCCGCCTCCTGAGTAGCTGGGACTACAGGCGTGCA T G C20orf194 Ensembl:ENSG00000088854 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1164723800 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92694,RMVar_hsa_circ_208432,RMVar_hsa_circ_18157,RMVar_hsa_circ_63181,RMVar_hsa_circ_127380,RMVar_hsa_circ_208442,RMVar_hsa_circ_208445,RMVar_hsa_circ_32128,RMVar_hsa_circ_104008,RMVar_hsa_circ_208444,RMVar_hsa_circ_74113,RMVar_hsa_circ_47609,RMVar_hsa_circ_54018,RMVar_hsa_circ_305716,RMVar_hsa_circ_208446,RMVar_hsa_circ_271883,RMVar_hsa_circ_282806,RMVar_hsa_circ_270355,RMVar_hsa_circ_208448,RMVar_hsa_circ_208449,RMVar_hsa_circ_208447 21595 RMVar_ID_21595 Human_SNP_ID_671912667 A-to-I Human chr20 + 3483383 3483383 3483383 CATTCTTTTTTTTTGTGACAGGGTCTCACTCTATGAACCAGGCTAGAGTGCAGTGATGTAATCAC CATTCTTTTTTTTTGTGACAGGGTCTCACTCTGTGAACCAGGCTAGAGTGCAGTGATGTAATCAC A G ATRN Ensembl:ENSG00000088812 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs577974773 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98188,RMVar_hsa_circ_208453 21596 RMVar_ID_21596 Human_SNP_ID_671932160 A-to-I Human chr20 + 3561973 3561973 3561973 GGCCAACATAGCAGGCCTCAAGTGATCCTCCCACCTTAGCCTCCCAAAGTGCTGGGATTACACAT GGCCAACATAGCAGGCCTCAAGTGATCCTCCCGCCTTAGCCTCCCAAAGTGCTGGGATTACACAT A G ATRN Ensembl:ENSG00000088812 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1356699664 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47689,RMVar_hsa_circ_98188,RMVar_hsa_circ_208453,RMVar_hsa_circ_61340,RMVar_hsa_circ_97426,RMVar_hsa_circ_312090,RMVar_hsa_circ_120728,RMVar_hsa_circ_208456,RMVar_hsa_circ_208457,RMVar_hsa_circ_208455,RMVar_hsa_circ_99336,RMVar_hsa_circ_58365,RMVar_hsa_circ_338256,RMVar_hsa_circ_88641,RMVar_hsa_circ_208460,RMVar_hsa_circ_208461,RMVar_hsa_circ_208459,RMVar_hsa_circ_100646,RMVar_hsa_circ_121756,RMVar_hsa_circ_58188,RMVar_hsa_circ_208463,RMVar_hsa_circ_208464,RMVar_hsa_circ_110901,RMVar_hsa_circ_370147,RMVar_hsa_circ_4423,RMVar_hsa_circ_208466,RMVar_hsa_circ_208467,RMVar_hsa_circ_357433,RMVar_hsa_circ_208465,RMVar_hsa_circ_369881,RMVar_hsa_circ_208470,RMVar_hsa_circ_208469,RMVar_hsa_circ_319775,RMVar_hsa_circ_326383 21597 RMVar_ID_21597 Human_SNP_ID_671932161 A-to-I Human chr20 + 3561973 3561973 3561973 GGCCAACATAGCAGGCCTCAAGTGATCCTCCCACCTTAGCCTCCCAAAGTGCTGGGATTACACAT GGCCAACATAGCAGGCCTCAAGTGATCCTCCCTCCTTAGCCTCCCAAAGTGCTGGGATTACACAT A T ATRN Ensembl:ENSG00000088812 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1356699664 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47689,RMVar_hsa_circ_98188,RMVar_hsa_circ_208453,RMVar_hsa_circ_61340,RMVar_hsa_circ_97426,RMVar_hsa_circ_312090,RMVar_hsa_circ_120728,RMVar_hsa_circ_208456,RMVar_hsa_circ_208457,RMVar_hsa_circ_208455,RMVar_hsa_circ_99336,RMVar_hsa_circ_58365,RMVar_hsa_circ_338256,RMVar_hsa_circ_88641,RMVar_hsa_circ_208460,RMVar_hsa_circ_208461,RMVar_hsa_circ_208459,RMVar_hsa_circ_100646,RMVar_hsa_circ_121756,RMVar_hsa_circ_58188,RMVar_hsa_circ_208463,RMVar_hsa_circ_208464,RMVar_hsa_circ_110901,RMVar_hsa_circ_370147,RMVar_hsa_circ_4423,RMVar_hsa_circ_208466,RMVar_hsa_circ_208467,RMVar_hsa_circ_357433,RMVar_hsa_circ_208465,RMVar_hsa_circ_369881,RMVar_hsa_circ_208470,RMVar_hsa_circ_208469,RMVar_hsa_circ_319775,RMVar_hsa_circ_326383 21598 RMVar_ID_21598 Human_SNP_ID_671995772 A-to-I Human chr20 + 3798442 3798442 3798442 AGGTCTCTGCATGGATTCCCCCAGCCCTATGGACCCCCACATGGCGGAGCAGACGTGAGTAGAGA AGGTCTCTGCATGGATTCCCCCAGCCCTATGGGCCCCCACATGGCGGAGCAGACGTGAGTAGAGA A G CDC25B Ensembl:ENSG00000101224 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749796277 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9388569,Human_RBP_ID_18773041,Human_RBP_ID_19105902 Human_Splice_Rec_2057142,Human_Splice_Rec_2057143,Human_Splice_Rec_2057170,Human_Splice_Rec_2057171,Human_Splice_Rec_2057200,Human_Splice_Rec_2057201,Human_Splice_Rec_2057230,Human_Splice_Rec_2057231,Human_Splice_Rec_2057260,Human_Splice_Rec_2057261,Human_Splice_Rec_2057290,Human_Splice_Rec_2057291 Human_miRNA_ID_2297945 RMVar_hsa_circ_44790,RMVar_hsa_circ_94429,RMVar_hsa_circ_208498 21599 RMVar_ID_21599 Human_SNP_ID_672003727 A-to-I Human chr20 + 3824731 3824731 3824731 GAGGTGGTTGGACCACCTCAGGTCGGGAGTTCAAGACCAGCCTGGCCAACATAGTGAAACCCCAT GAGGTGGTTGGACCACCTCAGGTCGGGAGTTCGAGACCAGCCTGGCCAACATAGTGAAACCCCAT A G AP5S1 Ensembl:ENSG00000125843 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1289253866 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1265533,Human_miRNA_ID_1690109 RMVar_hsa_circ_127138,RMVar_hsa_circ_208505,RMVar_hsa_circ_80302,RMVar_hsa_circ_208507 21600 RMVar_ID_21600 Human_SNP_ID_672003745 A-to-I Human chr20 + 3824811 3824811 3824811 AAAAATTAGCTGGGTGTATGGCGCCCACCTGTAATCCTAGCTGCTCAGGGGGCTGAGTCATGGGA AAAAATTAGCTGGGTGTATGGCGCCCACCTGTGATCCTAGCTGCTCAGGGGGCTGAGTCATGGGA A G AP5S1 Ensembl:ENSG00000125843 Protein coding 3'UTR GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-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 21601 RMVar_ID_21601 Human_SNP_ID_672003749 A-to-I Human chr20 + 3824825 3824824 3824826 TGTATGGCGCCCACCTGTAATCCTAGCTGCTCAGGGGGCTGAGTCATGGGAATCACTTGAACCTG TGTATGGCGCCCACCTGTAATCCTAGCTGCTC__GGGGCTGAGTCATGGGAATCACTTGAACCTG CAG C AP5S1 Ensembl:ENSG00000125843 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs959797610 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_18444388 Human_miRNA_ID_120868,Human_miRNA_ID_124684,Human_miRNA_ID_960583,Human_miRNA_ID_1973926,Human_miRNA_ID_1976105,Human_miRNA_ID_2613896 RMVar_hsa_circ_127138,RMVar_hsa_circ_208505,RMVar_hsa_circ_80302,RMVar_hsa_circ_208507 21602 RMVar_ID_21602 Human_SNP_ID_672003751 A-to-I Human chr20 + 3824825 3824825 3824825 TGTATGGCGCCCACCTGTAATCCTAGCTGCTCAGGGGGCTGAGTCATGGGAATCACTTGAACCTG TGTATGGCGCCCACCTGTAATCCTAGCTGCTCGGGGGGCTGAGTCATGGGAATCACTTGAACCTG A G AP5S1 Ensembl:ENSG00000125843 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1341444028 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18444388 Human_miRNA_ID_120868,Human_miRNA_ID_124684,Human_miRNA_ID_960583,Human_miRNA_ID_1973926,Human_miRNA_ID_1976105,Human_miRNA_ID_2613896 RMVar_hsa_circ_127138,RMVar_hsa_circ_208505,RMVar_hsa_circ_80302,RMVar_hsa_circ_208507 21603 RMVar_ID_21603 Human_SNP_ID_672003764 A-to-I Human chr20 + 3824864 3824864 3824864 TGAGTCATGGGAATCACTTGAACCTGGGAGGCAGAGTTTGCAGTGAGCCGAGAGTGCGCCACTTC TGAGTCATGGGAATCACTTGAACCTGGGAGGCGGAGTTTGCAGTGAGCCGAGAGTGCGCCACTTC A G AP5S1 Ensembl:ENSG00000125843 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1141191 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127138,RMVar_hsa_circ_208505,RMVar_hsa_circ_80302,RMVar_hsa_circ_208507 21604 RMVar_ID_21604 Human_SNP_ID_672004488 A-to-I Human chr20 + 3827526 3827526 3827526 CTTGTGATCCGCCCGCCGTGGCCTCTCAAAGTACCGGGATTATAGGCGTGAGCCACCACGACTGA CTTGTGATCCGCCCGCCGTGGCCTCTCAAAGTGCCGGGATTATAGGCGTGAGCCACCACGACTGA A G AP5S1 Ensembl:ENSG00000125843 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1370909656 Functional Loss SNV dbSNP153 33..33 33 - - - 21605 RMVar_ID_21605 Human_SNP_ID_672005128 A-to-I Human chr20 + 3830013 3830013 3830013 GCCCAGGAGTTCGAAACCAGCCTGTACAACATAGAGACTTCATCTCTACAAAAAAATATAAAAAT GCCCAGGAGTTCGAAACCAGCCTGTACAACATGGAGACTTCATCTCTACAAAAAAATATAAAAAT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1469855896 Functional Loss SNV dbSNP153 33..33 33 - - - 21606 RMVar_ID_21606 Human_SNP_ID_672008498 A-to-I Human chr20 + 3841351 3841351 3841351 CTCCCGCCTCAGCCTCCCAGGTAGCCGAGACTAGAGGAGCGTGCCACCATGCCTGGCTAATTTTT CTCCCGCCTCAGCCTCCCAGGTAGCCGAGACTGGAGGAGCGTGCCACCATGCCTGGCTAATTTTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs896216696 Functional Loss SNV dbSNP153 33..33 33 - - - 21607 RMVar_ID_21607 Human_SNP_ID_672012251 A-to-I Human chr20 + 3853657 3853657 3853657 CTCTAGAAAAAATAAAAAAATTAGCTGGGCATAGTGGCGCAGGTTTGTAGTTCCAGCTACCGGGG CTCTAGAAAAAATAAAAAAATTAGCTGGGCATTGTGGCGCAGGTTTGTAGTTCCAGCTACCGGGG A T MAVS Ensembl:ENSG00000088888 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs978501874 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17572015 21608 RMVar_ID_21608 Human_SNP_ID_672012256 A-to-I Human chr20 + 3853673 3853673 3853673 AAAATTAGCTGGGCATAGTGGCGCAGGTTTGTAGTTCCAGCTACCGGGGATGCTGAGGCGGGAGG AAAATTAGCTGGGCATAGTGGCGCAGGTTTGTGGTTCCAGCTACCGGGGATGCTGAGGCGGGAGG A G MAVS Ensembl:ENSG00000088888 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1318638271 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571803 21609 RMVar_ID_21609 Human_SNP_ID_672012276 A-to-I Human chr20 + 3853735 3853735 3853735 AGGATTGCTTGAGCCCACGAGTTCGAGGCTGCAGTGAACTATTATTGCACCACTGCACCCAACTT AGGATTGCTTGAGCCCACGAGTTCGAGGCTGCTGTGAACTATTATTGCACCACTGCACCCAACTT A T MAVS Ensembl:ENSG00000088888 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1378071982 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571803,Human_RBP_ID_23184206 21610 RMVar_ID_21610 Human_SNP_ID_672013194 A-to-I Human chr20 + 3856617 3856617 3856617 TGTGATCCTCGGCCTTCCAAAGTGCTGGGATTACGGGTGTGAGCTACCGCACCTGGCTATTTTCC TGTGATCCTCGGCCTTCCAAAGTGCTGGGATTGCGGGTGTGAGCTACCGCACCTGGCTATTTTCC A G MAVS Ensembl:ENSG00000088888 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs997288030 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_290874,RMVar_hsa_circ_340533,RMVar_hsa_circ_208509,RMVar_hsa_circ_282942,RMVar_hsa_circ_208508 21611 RMVar_ID_21611 Human_SNP_ID_672013939 A-to-I Human chr20 + 3858817 3858817 3858817 TTTCTTTCTCTCTCTTTTTTTTTTTTCCTTTTAGAGACAGAGTCTTGCTGCGCCACCCAGGCTGC TTTCTTTCTCTCTCTTTTTTTTTTTTCCTTTTGGAGACAGAGTCTTGCTGCGCCACCCAGGCTGC A G MAVS Ensembl:ENSG00000088888 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1369584991 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25626743 RMVar_hsa_circ_340533,RMVar_hsa_circ_208509,RMVar_hsa_circ_282942,RMVar_hsa_circ_326712 21612 RMVar_ID_21612 Human_SNP_ID_672013941 A-to-I Human chr20 + 3858823 3858822 3858824 TCTCTCTCTTTTTTTTTTTTCCTTTTAGAGACAGAGTCTTGCTGCGCCACCCAGGCTGCAGTGCA TCTCTCTCTTTTTTTTTTTTCCTTTTAGAGAC__AGTCTTGCTGCGCCACCCAGGCTGCAGTGCA CAG C MAVS Ensembl:ENSG00000088888 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1237766367 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_25626743 RMVar_hsa_circ_340533,RMVar_hsa_circ_208509,RMVar_hsa_circ_282942,RMVar_hsa_circ_326712 21613 RMVar_ID_21613 Human_SNP_ID_672013987 A-to-I Human chr20 + 3859000 3859000 3859000 TTTTAAATTTTTTGTAGAGATGACATCTCACTATGTTGCCCAGGCTGGTCTCAAACTCCTGGGCT TTTTAAATTTTTTGTAGAGATGACATCTCACTGTGTTGCCCAGGCTGGTCTCAAACTCCTGGGCT A G MAVS Ensembl:ENSG00000088888 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1236008571 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_340533,RMVar_hsa_circ_208509,RMVar_hsa_circ_282942,RMVar_hsa_circ_326712 21614 RMVar_ID_21614 Human_SNP_ID_672014817 A-to-I Human chr20 + 3860857 3860857 3860857 TGCCAGCACGCCTGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACTATGTTGGCCAGGC TGCCAGCACGCCTGGCTAATTTTTGTATTTTTGGTAGAGACGGGGTTTCACTATGTTGGCCAGGC A G MAVS Ensembl:ENSG00000088888 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1211511844 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_340533,RMVar_hsa_circ_208509,RMVar_hsa_circ_282942,RMVar_hsa_circ_326712 21615 RMVar_ID_21615 Human_SNP_ID_672014931 A-to-I Human chr20 + 3861178 3861178 3861178 CCATGCCCGGCTAATAATAATGTTGTATTTTTAGTAGAGATGGGGTTTCACTGTGTTAGCCAGGG CCATGCCCGGCTAATAATAATGTTGTATTTTTGGTAGAGATGGGGTTTCACTGTGTTAGCCAGGG A G MAVS Ensembl:ENSG00000088888 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs543924627 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_340533,RMVar_hsa_circ_208509,RMVar_hsa_circ_282942,RMVar_hsa_circ_326712 21616 RMVar_ID_21616 Human_SNP_ID_672014932 A-to-I Human chr20 + 3861178 3861178 3861178 CCATGCCCGGCTAATAATAATGTTGTATTTTTAGTAGAGATGGGGTTTCACTGTGTTAGCCAGGG CCATGCCCGGCTAATAATAATGTTGTATTTTTTGTAGAGATGGGGTTTCACTGTGTTAGCCAGGG A T MAVS Ensembl:ENSG00000088888 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs543924627 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_340533,RMVar_hsa_circ_208509,RMVar_hsa_circ_282942,RMVar_hsa_circ_326712 21617 RMVar_ID_21617 Human_SNP_ID_672016674 A-to-I Human chr20 + 3867455 3867455 3867455 CCATCTCTACAAAAAAGTTTAAAAAATTAGCCAGGCGTGGTGGTGCACCTGTCGTCTTAGCTACT CCATCTCTACAAAAAAGTTTAAAAAATTAGCCCGGCGTGGTGGTGCACCTGTCGTCTTAGCTACT A C MAVS Ensembl:ENSG00000088888 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,31158229,31158229,32596459 RNA-Seq:(High) rs946390493 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8204485,Human_RBP_ID_22600814,Human_RBP_ID_25611704,Human_RBP_ID_26492875 Human_miRNA_ID_337057 21618 RMVar_ID_21618 Human_SNP_ID_672016688 A-to-I Human chr20 + 3867516 3867516 3867516 TACTTGGGAGGCTGAGGTGGGAGGATCACTTGAGCCCAGAAGCTTGAAGCTGCAGTGAGCTAGGA TACTTGGGAGGCTGAGGTGGGAGGATCACTTGCGCCCAGAAGCTTGAAGCTGCAGTGAGCTAGGA A C MAVS Ensembl:ENSG00000088888 Protein coding 3'UTR GSE47997;GSE99789;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,29796672,31158229,32596459 RNA-Seq:(High) rs1452650508 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1158676 21619 RMVar_ID_21619 Human_SNP_ID_672016694 A-to-I Human chr20 + 3867545 3867545 3867545 TTGAGCCCAGAAGCTTGAAGCTGCAGTGAGCTAGGATCGTGCCACTGCACTCCAACCTGGGTGAG TTGAGCCCAGAAGCTTGAAGCTGCAGTGAGCTGGGATCGTGCCACTGCACTCCAACCTGGGTGAG A G MAVS Ensembl:ENSG00000088888 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490829,GSM3490830,GSM3490831 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,EC109 cell line - 23474544,24183664,29129909,31158229,31158229,32596459 RNA-Seq:(High) rs1018291426 Functional Loss SNV dbSNP153 33..33 33 - - - 21620 RMVar_ID_21620 Human_SNP_ID_672016902 A-to-I Human chr20 + 3868410 3868410 3868410 TAATCCCAGCACTTTGGGAGGCCAAGGTGGGCAGATCGCCTGAGGTCTGGAGTTCAAGACCAGCC TAATCCCAGCACTTTGGGAGGCCAAGGTGGGCGGATCGCCTGAGGTCTGGAGTTCAAGACCAGCC A G MAVS Ensembl:ENSG00000088888 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs897401367 Functional Loss SNV dbSNP153 33..33 33 - - - 21621 RMVar_ID_21621 Human_SNP_ID_672016915 A-to-I Human chr20 + 3868478 3868477 3868478 CCAACAGGGTGAAACCCCGTCTCTACAAAAATAAGAAAATTAGCCAGGTGTAGTGGCAGACGTCT CCAACAGGGTGAAACCCCGTCTCTACAAAAAT_AGAAAATTAGCCAGGTGTAGTGGCAGACGTCT TA T MAVS Ensembl:ENSG00000088888 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1227754469 Functional Loss DEL dbSNP153 33..33 33 - - - 21622 RMVar_ID_21622 Human_SNP_ID_672016918 A-to-I Human chr20 + 3868503 3868503 3868503 CAAAAATAAGAAAATTAGCCAGGTGTAGTGGCAGACGTCTGTAATCCCAGCTATTCAGGAGGCTG CAAAAATAAGAAAATTAGCCAGGTGTAGTGGCGGACGTCTGTAATCCCAGCTATTCAGGAGGCTG A G MAVS Ensembl:ENSG00000088888 Protein coding 3'UTR GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs1471960581 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14105955 Human_miRNA_ID_1009600 21623 RMVar_ID_21623 Human_SNP_ID_672016936 A-to-I Human chr20 + 3868575 3868575 3868575 AGAATTCCATGAACCCAGGATGCGGAGGTTGCAGTGAGCCGAGATTGTGCCACTGCGCTCCAGCC AGAATTCCATGAACCCAGGATGCGGAGGTTGCGGTGAGCCGAGATTGTGCCACTGCGCTCCAGCC A G MAVS Ensembl:ENSG00000088888 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1204557404 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22722847,Human_RBP_ID_25611719,Human_RBP_ID_26490419 Human_miRNA_ID_612849 21624 RMVar_ID_21624 Human_SNP_ID_672016952 A-to-I Human chr20 + 3868616 3868616 3868616 AGATTGTGCCACTGCGCTCCAGCCTGGGCGACAGAGTGGTATTCTGTTTCAAAAAAAAAAAAAAA AGATTGTGCCACTGCGCTCCAGCCTGGGCGACCGAGTGGTATTCTGTTTCAAAAAAAAAAAAAAA A C MAVS Ensembl:ENSG00000088888 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1252130323 Functional Loss SNV dbSNP153 33..33 33 - - - 21625 RMVar_ID_21625 Human_SNP_ID_672016953 A-to-I Human chr20 + 3868616 3868616 3868616 AGATTGTGCCACTGCGCTCCAGCCTGGGCGACAGAGTGGTATTCTGTTTCAAAAAAAAAAAAAAA AGATTGTGCCACTGCGCTCCAGCCTGGGCGACGGAGTGGTATTCTGTTTCAAAAAAAAAAAAAAA A G MAVS Ensembl:ENSG00000088888 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1252130323 Functional Loss SNV dbSNP153 33..33 33 - - - 21626 RMVar_ID_21626 Human_SNP_ID_672016993 A-to-I Human chr20 + 3868710 3868710 3868710 CAAGTGGTAGAATGTTAGCACACTACCAGCCTAGGTAAAAAATACAAAAAGTAACTGGGCATGGC CAAGTGGTAGAATGTTAGCACACTACCAGCCTCGGTAAAAAATACAAAAAGTAACTGGGCATGGC A C MAVS Ensembl:ENSG00000088888 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs758259347 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23184227 21627 RMVar_ID_21627 Human_SNP_ID_672017098 A-to-I Human chr20 + 3869082 3869082 3869082 GAAGTGGTGCAATCATAACTCACTGTATCCTTAAACTCCCGGGCTTAAGCGATCCTCCTGCCTCA GAAGTGGTGCAATCATAACTCACTGTATCCTTGAACTCCCGGGCTTAAGCGATCCTCCTGCCTCA A G MAVS Ensembl:ENSG00000088888 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1466095937 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7000868,Human_RBP_ID_14105972,Human_RBP_ID_17971702 21628 RMVar_ID_21628 Human_SNP_ID_672017181 A-to-I Human chr20 + 3869355 3869355 3869355 CCACCACGCCTGGCTAATTTTTTTGCACTTTTAGTAGAGACGGGGTTTCACTGTGTTAGCCAGGA CCACCACGCCTGGCTAATTTTTTTGCACTTTTGGTAGAGACGGGGTTTCACTGTGTTAGCCAGGA A G MAVS Ensembl:ENSG00000088888 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1344677062 Functional Loss SNV dbSNP153 33..33 33 - - - 21629 RMVar_ID_21629 Human_SNP_ID_672017194 A-to-I Human chr20 + 3869380 3869380 3869380 CACTTTTAGTAGAGACGGGGTTTCACTGTGTTAGCCAGGATGGTCTCGATCTCCTGACCTTGTGA CACTTTTAGTAGAGACGGGGTTTCACTGTGTTGGCCAGGATGGTCTCGATCTCCTGACCTTGTGA A G MAVS Ensembl:ENSG00000088888 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs925557770 Functional Loss SNV dbSNP153 33..33 33 - - - 21630 RMVar_ID_21630 Human_SNP_ID_672017255 A-to-I Human chr20 + 3869566 3869566 3869566 ATCTTGCCTTAGCCTCCCAAAGTGCTGGGATTACAGATGTGAGACACTGCACCCAAACCCCACCA ATCTTGCCTTAGCCTCCCAAAGTGCTGGGATTGCAGATGTGAGACACTGCACCCAAACCCCACCA A G MAVS Ensembl:ENSG00000088888 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs112574694 Functional Loss SNV dbSNP153 33..33 33 - - - 21631 RMVar_ID_21631 Human_SNP_ID_672017256 A-to-I Human chr20 + 3869566 3869566 3869566 ATCTTGCCTTAGCCTCCCAAAGTGCTGGGATTACAGATGTGAGACACTGCACCCAAACCCCACCA ATCTTGCCTTAGCCTCCCAAAGTGCTGGGATTTCAGATGTGAGACACTGCACCCAAACCCCACCA A T MAVS Ensembl:ENSG00000088888 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs112574694 Functional Loss SNV dbSNP153 33..33 33 - - - 21632 RMVar_ID_21632 Human_SNP_ID_672017278 A-to-I Human chr20 + 3869630 3869630 3869630 ACTTTTTTTTTTCCTTTTTCTTTTTTTGAGACAGTCTTACTCCGTTGCCCAGGCTGGAGTGTAGT ACTTTTTTTTTTCCTTTTTCTTTTTTTGAGACCGTCTTACTCCGTTGCCCAGGCTGGAGTGTAGT A C MAVS Ensembl:ENSG00000088888 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1568540594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14105982,Human_RBP_ID_17572023,Human_RBP_ID_23184241,Human_RBP_ID_26493378 21633 RMVar_ID_21633 Human_SNP_ID_672017307 A-to-I Human chr20 + 3869746 3869746 3869746 CCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGAGGCCTGCCACCACACCCGACTAATTTTCGT CCTGCCTCAGCCTCCCGAGTAGCTGGGATTACGGAGGCCTGCCACCACACCCGACTAATTTTCGT A G MAVS Ensembl:ENSG00000088888 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs958293529 Functional Loss SNV dbSNP153 33..33 33 - - - 21634 RMVar_ID_21634 Human_SNP_ID_672017334 A-to-I Human chr20 + 3869865 3869864 3869865 GACCTCAAGTGCTCCACCTGCGTTGGCTTCCCAAAGTGCTGGGATACAGGAGTGAGCCACTGCGC GACCTCAAGTGCTCCACCTGCGTTGGCTTCCC_AAGTGCTGGGATACAGGAGTGAGCCACTGCGC CA C MAVS Ensembl:ENSG00000088888 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1166282588 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_23184243 21635 RMVar_ID_21635 Human_SNP_ID_672017335 A-to-I Human chr20 + 3869866 3869866 3869866 ACCTCAAGTGCTCCACCTGCGTTGGCTTCCCAAAGTGCTGGGATACAGGAGTGAGCCACTGCGCC ACCTCAAGTGCTCCACCTGCGTTGGCTTCCCAGAGTGCTGGGATACAGGAGTGAGCCACTGCGCC A G MAVS Ensembl:ENSG00000088888 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1137153 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4647334,Human_RBP_ID_23184243 21636 RMVar_ID_21636 Human_SNP_ID_672017506 A-to-I Human chr20 + 3870629 3870629 3870629 TGAGACAAGCCTGGGCAACAAAGCAAGACCCTATCTCTAAAAAAAAAAAAAAAAAAAAAAAAAAA TGAGACAAGCCTGGGCAACAAAGCAAGACCCTCTCTCTAAAAAAAAAAAAAAAAAAAAAAAAAAA A C MAVS Ensembl:ENSG00000088888 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs897908148 Functional Loss SNV dbSNP153 33..33 33 - - - 21637 RMVar_ID_21637 Human_SNP_ID_672017617 A-to-I Human chr20 + 3870904 3870903 3870905 CTCATTCTGCAGAGGTTCTTTTCTTTTGAGACAGAGTGTTGCTCTGTTGCCCAGGCTGGAGTGCA CTCATTCTGCAGAGGTTCTTTTCTTTTGAGAC__AGTGTTGCTCTGTTGCCCAGGCTGGAGTGCA CAG C MAVS Ensembl:ENSG00000088888 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,31158229,32596459,32596459 RNA-Seq:(High) rs554087729 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_564006,Human_RBP_ID_22371397 21638 RMVar_ID_21638 Human_SNP_ID_672017648 A-to-I Human chr20 + 3870998 3870998 3870998 CGCCTCCCAGGTTCAAGTGATTCTCCTGCTTCAGCCTCTCAAGTAGCTGGGATTACAGATGCCCG CGCCTCCCAGGTTCAAGTGATTCTCCTGCTTCGGCCTCTCAAGTAGCTGGGATTACAGATGCCCG A G MAVS Ensembl:ENSG00000088888 Protein coding 3'UTR GSE38233;GSE100210;GSE99789;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;ASD brains,Fragile X samples from NIH NeuroBioBank;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,29796672,30559470,31158229,32596459 RNA-Seq:(High) rs1271352646 Functional Loss SNV dbSNP153 33..33 33 - - - 21639 RMVar_ID_21639 Human_SNP_ID_672017651 A-to-I Human chr20 + 3871006 3871006 3871006 AGGTTCAAGTGATTCTCCTGCTTCAGCCTCTCAAGTAGCTGGGATTACAGATGCCCGCCACCACA AGGTTCAAGTGATTCTCCTGCTTCAGCCTCTCGAGTAGCTGGGATTACAGATGCCCGCCACCACA A G MAVS Ensembl:ENSG00000088888 Protein coding 3'UTR GSE38233;GSE99789;GSE107867;GSE107867 cultured B-cells;esophageal squamous carcinoma cells,EC109;ASD brains,cerebellum;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 24183664,29796672,30559470,30559470 RNA-Seq:(High) rs570582147 Functional Loss SNV dbSNP153 33..33 33 - - - 21640 RMVar_ID_21640 Human_SNP_ID_672017673 A-to-I Human chr20 + 3871046 3871046 3871046 GGGATTACAGATGCCCGCCACCACACCTGGCTAATTTTCGTATTTTTGTTAGAGATGGGGTTTCA GGGATTACAGATGCCCGCCACCACACCTGGCTGATTTTCGTATTTTTGTTAGAGATGGGGTTTCA A G MAVS Ensembl:ENSG00000088888 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs765509714 Functional Loss SNV dbSNP153 33..33 33 - - - 21641 RMVar_ID_21641 Human_SNP_ID_672017927 A-to-I Human chr20 + 3872176 3872176 3872176 TAAAGTGAGATTTTGGCTGGAGGTGGTGGATCATACCTATAATCCCAGCACTTTGGGAGACCAAG TAAAGTGAGATTTTGGCTGGAGGTGGTGGATCCTACCTATAATCCCAGCACTTTGGGAGACCAAG A C MAVS Ensembl:ENSG00000088888 Protein coding 3'UTR GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs902921717 Functional Loss SNV dbSNP153 33..33 33 - - - 21642 RMVar_ID_21642 Human_SNP_ID_672017928 A-to-I Human chr20 + 3872176 3872176 3872176 TAAAGTGAGATTTTGGCTGGAGGTGGTGGATCATACCTATAATCCCAGCACTTTGGGAGACCAAG TAAAGTGAGATTTTGGCTGGAGGTGGTGGATCTTACCTATAATCCCAGCACTTTGGGAGACCAAG A T MAVS Ensembl:ENSG00000088888 Protein coding 3'UTR GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs902921717 Functional Loss SNV dbSNP153 33..33 33 - - - 21643 RMVar_ID_21643 Human_SNP_ID_672017966 A-to-I Human chr20 + 3872413 3872413 3872413 TGAGCTATGATGGCACCACTGCACTTCAGCCTAGGCAACAGAGGGAGACCCTGTCTTTAAAGTAC TGAGCTATGATGGCACCACTGCACTTCAGCCTGGGCAACAGAGGGAGACCCTGTCTTTAAAGTAC A G MAVS Ensembl:ENSG00000088888 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11551648 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26490429 21644 RMVar_ID_21644 Human_SNP_ID_672018174 A-to-I Human chr20 + 3873380 3873380 3873380 ACATGGTGAAACCCCATCTGTACTAAAAATACAAAAATTAGCCAGGTGTGATGGCGTACATCTGT ACATGGTGAAACCCCATCTGTACTAAAAATACCAAAATTAGCCAGGTGTGATGGCGTACATCTGT A C MAVS Ensembl:ENSG00000088888 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1369717652 Functional Loss SNV dbSNP153 33..33 33 - - - 21645 RMVar_ID_21645 Human_SNP_ID_672018177 A-to-I Human chr20 + 3873398 3873398 3873398 TGTACTAAAAATACAAAAATTAGCCAGGTGTGATGGCGTACATCTGTAATTTCAGCCACTCGGGA TGTACTAAAAATACAAAAATTAGCCAGGTGTGGTGGCGTACATCTGTAATTTCAGCCACTCGGGA A G MAVS Ensembl:ENSG00000088888 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs939203714 Functional Loss SNV dbSNP153 33..33 33 - - - 21646 RMVar_ID_21646 Human_SNP_ID_672018191 A-to-I Human chr20 + 3873459 3873459 3873459 GGGAGGCTGAGACAGGAGAATAGCTTGAACCCAGTAGGTGGAGATTTCAGTGAGCCGAGATCGTG GGGAGGCTGAGACAGGAGAATAGCTTGAACCCGGTAGGTGGAGATTTCAGTGAGCCGAGATCGTG A G MAVS Ensembl:ENSG00000088888 Protein coding 3'UTR GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,31158229,32596459 RNA-Seq:(High) rs891149569 Functional Loss SNV dbSNP153 33..33 33 - - - 21647 RMVar_ID_21647 Human_SNP_ID_672018612 A-to-I Human chr20 + 3875287 3875287 3875287 AAAATAGTTAATTTAGCCAGGCATGATGATATATGCCTGTAGTCCCAACTACTTGGAAGGCTGAG AAAATAGTTAATTTAGCCAGGCATGATGATATGTGCCTGTAGTCCCAACTACTTGGAAGGCTGAG A G MAVS Ensembl:ENSG00000088888 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs540696546 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_564029,Human_RBP_ID_4663645,Human_RBP_ID_17971724,Human_RBP_ID_26492884 21648 RMVar_ID_21648 Human_SNP_ID_672018615 A-to-I Human chr20 + 3875295 3875295 3875295 TAATTTAGCCAGGCATGATGATATATGCCTGTAGTCCCAACTACTTGGAAGGCTGAGGTGTGAGG TAATTTAGCCAGGCATGATGATATATGCCTGTGGTCCCAACTACTTGGAAGGCTGAGGTGTGAGG A G MAVS Ensembl:ENSG00000088888 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1132927 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_564029,Human_RBP_ID_17971724,Human_RBP_ID_26492884 21649 RMVar_ID_21649 Human_SNP_ID_672018630 A-to-I Human chr20 + 3875359 3875359 3875359 GATCTTTGAGCCCGGGAGGTCGAGGCTACAGTAAGCTATGATCTCACCACTGTACTCCAGCCTGG GATCTTTGAGCCCGGGAGGTCGAGGCTACAGTGAGCTATGATCTCACCACTGTACTCCAGCCTGG A G MAVS Ensembl:ENSG00000088888 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1071671 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25611781,Human_RBP_ID_26490432 21650 RMVar_ID_21650 Human_SNP_ID_672018951 A-to-I Human chr20 + 3876404 3876404 3876404 TTTTTTTTTTTTTTAAGACAAGGGCATGCTCTATCGCCCAGGTTGGAGTAGAGTGGAGTAGAATG TTTTTTTTTTTTTTAAGACAAGGGCATGCTCTGTCGCCCAGGTTGGAGTAGAGTGGAGTAGAATG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1219144758 Functional Loss SNV dbSNP153 33..33 33 - - - 21651 RMVar_ID_21651 Human_SNP_ID_672022670 A-to-I Human chr20 - 3888345 3888345 3888345 GGGCGTGGTGGCCCATGCCTATAATCCCAGCTACTTGGGAAGCTGAGGCAGGAAAATTGCTTGAA GGGCGTGGTGGCCCATGCCTATAATCCCAGCTTCTTGGGAAGCTGAGGCAGGAAAATTGCTTGAA T A PANK2-AS1 Ensembl:ENSG00000229539 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1476610941 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18773121 21652 RMVar_ID_21652 Human_SNP_ID_672022673 A-to-I Human chr20 - 3888354 3888354 3888354 GTATTAGCGGGGCGTGGTGGCCCATGCCTATAATCCCAGCTACTTGGGAAGCTGAGGCAGGAAAA GTATTAGCGGGGCGTGGTGGCCCATGCCTATACTCCCAGCTACTTGGGAAGCTGAGGCAGGAAAA T G PANK2-AS1 Ensembl:ENSG00000229539 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1039943814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18773121 21653 RMVar_ID_21653 Human_SNP_ID_672022674 A-to-I Human chr20 - 3888357 3888357 3888357 TCCGTATTAGCGGGGCGTGGTGGCCCATGCCTATAATCCCAGCTACTTGGGAAGCTGAGGCAGGA TCCGTATTAGCGGGGCGTGGTGGCCCATGCCTGTAATCCCAGCTACTTGGGAAGCTGAGGCAGGA T C PANK2-AS1 Ensembl:ENSG00000229539 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1453443070 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18773121 21654 RMVar_ID_21654 Human_SNP_ID_672023936 A-to-I Human chr20 + 3891167 3891155 3891168 AACCTCCTGGGCTCAAGCCATCCTCCTGCTTCAACCTCCTGCATTGCTGGGACTAAAGGCACGTG AACCTCCTGGGCTCAAGCCAT_____________CCTCCTGCATTGCTGGGACTAAAGGCACGTG TCCTCCTGCTTCAA T PANK2 Ensembl:ENSG00000125779 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935159481 Functional Loss DEL dbSNP153 22..34 33 - - - RMVar_hsa_circ_85386,RMVar_hsa_circ_208515 21655 RMVar_ID_21655 Human_SNP_ID_672023943 A-to-I Human chr20 + 3891189 3891189 3891189 CTCCTGCTTCAACCTCCTGCATTGCTGGGACTAAAGGCACGTGCCACTATGCCAGGCTAATTTTT CTCCTGCTTCAACCTCCTGCATTGCTGGGACTGAAGGCACGTGCCACTATGCCAGGCTAATTTTT A G PANK2 Ensembl:ENSG00000125779 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1378743011 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85386,RMVar_hsa_circ_208515 21656 RMVar_ID_21656 Human_SNP_ID_672023976 A-to-I Human chr20 + 3891295 3891295 3891295 GCCCAGGCTGGTCTTGAATTCCTCCTGGTCTCAAGCGATCTTCCCACTTCGGCCTCCCAAAGTGC GCCCAGGCTGGTCTTGAATTCCTCCTGGTCTCTAGCGATCTTCCCACTTCGGCCTCCCAAAGTGC A T PANK2 Ensembl:ENSG00000125779 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs977261441 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2057432 RMVar_hsa_circ_46123,RMVar_hsa_circ_85386,RMVar_hsa_circ_208515,RMVar_hsa_circ_15339 21657 RMVar_ID_21657 Human_SNP_ID_672025943 A-to-I Human chr20 + 3897840 3897840 3897840 ACCAGCTTGGTCAACATGGTGAAACTGTCTCTACTAAAAATATGAAAACTAGCTGGGCATGGTGG ACCAGCTTGGTCAACATGGTGAAACTGTCTCTGCTAAAAATATGAAAACTAGCTGGGCATGGTGG A G PANK2 Ensembl:ENSG00000125779 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs950302231 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_46123,RMVar_hsa_circ_85386,RMVar_hsa_circ_208515,RMVar_hsa_circ_208516,RMVar_hsa_circ_15339 21658 RMVar_ID_21658 Human_SNP_ID_672026106 A-to-I Human chr20 + 3898400 3898400 3898400 TTTTGTATTTTTAGTAGAGATGGGGTTTTACCATGTCGGCCAGACTGGTCTCGAACTCCTGACCT TTTTGTATTTTTAGTAGAGATGGGGTTTTACCGTGTCGGCCAGACTGGTCTCGAACTCCTGACCT A G PANK2 Ensembl:ENSG00000125779 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs576694349 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_46123,RMVar_hsa_circ_85386,RMVar_hsa_circ_208515,RMVar_hsa_circ_208516,RMVar_hsa_circ_15339 21659 RMVar_ID_21659 Human_SNP_ID_672026970 A-to-I Human chr20 + 3901494 3901494 3901494 CTAAATTTTGACACATTTAAACTATCACTTCTATATTCTTGTGTAGAATTAATCAGAATCTATCT CTAAATTTTGACACATTTAAACTATCACTTCTGTATTCTTGTGTAGAATTAATCAGAATCTATCT A G PANK2 Ensembl:ENSG00000125779 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6107367 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_46123,RMVar_hsa_circ_85386,RMVar_hsa_circ_208515,RMVar_hsa_circ_208516,RMVar_hsa_circ_15339 21660 RMVar_ID_21660 Human_SNP_ID_672026971 A-to-I Human chr20 + 3901494 3901494 3901494 CTAAATTTTGACACATTTAAACTATCACTTCTATATTCTTGTGTAGAATTAATCAGAATCTATCT CTAAATTTTGACACATTTAAACTATCACTTCTTTATTCTTGTGTAGAATTAATCAGAATCTATCT A T PANK2 Ensembl:ENSG00000125779 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6107367 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_46123,RMVar_hsa_circ_85386,RMVar_hsa_circ_208515,RMVar_hsa_circ_208516,RMVar_hsa_circ_15339 21661 RMVar_ID_21661 Human_SNP_ID_672027554 A-to-I Human chr20 + 3903400 3903400 3903400 GAATTCCTGACCTCAGGTGATCCGCCCGCCTTAGCCTCCCAAAGTGCTGGAATTACAGGCATGAG GAATTCCTGACCTCAGGTGATCCGCCCGCCTTTGCCTCCCAAAGTGCTGGAATTACAGGCATGAG A T PANK2 Ensembl:ENSG00000125779 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs533266700 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_46123,RMVar_hsa_circ_85386,RMVar_hsa_circ_208515,RMVar_hsa_circ_208516,RMVar_hsa_circ_15339 21662 RMVar_ID_21662 Human_SNP_ID_672028133 A-to-I Human chr20 + 3905451 3905451 3905451 CCGCTCACTGCTCCGCCTCCCGGGTTCATGCCATTCTCCTGCCTCAGCCTGCTGAGTAGCTGGGA CCGCTCACTGCTCCGCCTCCCGGGTTCATGCCCTTCTCCTGCCTCAGCCTGCTGAGTAGCTGGGA A C PANK2 Ensembl:ENSG00000125779 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1169221925 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_46123,RMVar_hsa_circ_85386,RMVar_hsa_circ_208515,RMVar_hsa_circ_208516,RMVar_hsa_circ_15339 21663 RMVar_ID_21663 Human_SNP_ID_672028230 A-to-I Human chr20 + 3905735 3905735 3905735 AATAAACCCACACCCTTTTTTTTTTTTTTTTGAGGTGGAGTTTTGCTCTGTCACCCAGGCTGTAG AATAAACCCACACCCTTTTTTTTTTTTTTTTGTGGTGGAGTTTTGCTCTGTCACCCAGGCTGTAG A T PANK2 Ensembl:ENSG00000125779 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1327435579 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_46123,RMVar_hsa_circ_85386,RMVar_hsa_circ_208515,RMVar_hsa_circ_208516,RMVar_hsa_circ_15339 21664 RMVar_ID_21664 Human_SNP_ID_672028367 A-to-I Human chr20 + 3906169 3906169 3906169 AAATCAGGCTGGGCGCAGTGGTTCACACTTGTAATCCCAGCACTTTGGGAGGCTGACCTGGGTGG AAATCAGGCTGGGCGCAGTGGTTCACACTTGTTATCCCAGCACTTTGGGAGGCTGACCTGGGTGG A T PANK2 Ensembl:ENSG00000125779 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1340673475 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571350 RMVar_hsa_circ_46123,RMVar_hsa_circ_85386,RMVar_hsa_circ_208515,RMVar_hsa_circ_208516,RMVar_hsa_circ_15339 21665 RMVar_ID_21665 Human_SNP_ID_672028397 A-to-I Human chr20 + 3906349 3906349 3906349 AGGAGGCTGAGATAGGAGGATTACTTGAGCCCAGGAGGCAGAGGTTGCAGTGAGCTGAGATTGTG AGGAGGCTGAGATAGGAGGATTACTTGAGCCCGGGAGGCAGAGGTTGCAGTGAGCTGAGATTGTG A G PANK2 Ensembl:ENSG00000125779 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1187926895 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_46123,RMVar_hsa_circ_85386,RMVar_hsa_circ_208515,RMVar_hsa_circ_208516,RMVar_hsa_circ_15339 21666 RMVar_ID_21666 Human_SNP_ID_672029677 A-to-I Human chr20 + 3910799 3910799 3910799 GCTCAGGGGTTAGCATCTTAGCAGTATATTCCAAAGATAATTACAAACGGGTCACAGGTACTAGG GCTCAGGGGTTAGCATCTTAGCAGTATATTCCCAAGATAATTACAAACGGGTCACAGGTACTAGG A C PANK2 Ensembl:ENSG00000125779 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1193312764 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_564045,Human_RBP_ID_1929777,Human_RBP_ID_5200586,Human_RBP_ID_27701894,Human_RBP_ID_27840649 Human_Splice_Rec_2057403,Human_Splice_Rec_2057413,Human_Splice_Rec_2057423,Human_Splice_Rec_2057437,Human_Splice_Rec_2057447,Human_Splice_Rec_2057459,Human_Splice_Rec_2057473,Human_Splice_Rec_2057485,Human_Splice_Rec_2057497 Human_miRNA_ID_33147 RMVar_hsa_circ_208517,RMVar_hsa_circ_46123,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,RMVar_hsa_circ_208521,RMVar_hsa_circ_208523,RMVar_hsa_circ_280579,RMVar_hsa_circ_294639,RMVar_hsa_circ_299925,RMVar_hsa_circ_288766,RMVar_hsa_circ_208524,RMVar_hsa_circ_208522 21667 RMVar_ID_21667 Human_SNP_ID_672030302 A-to-I Human chr20 + 3912829 3912829 3912829 AAAATTAGCTAGGCATGGTGGTGCGCGCCTGTAGACCCAGGTACTTGGGAGGCTGAGGCAGGAGA AAAATTAGCTAGGCATGGTGGTGCGCGCCTGTTGACCCAGGTACTTGGGAGGCTGAGGCAGGAGA A T PANK2 Ensembl:ENSG00000125779 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs990728739 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571351 RMVar_hsa_circ_208517,RMVar_hsa_circ_15339,RMVar_hsa_circ_287845,RMVar_hsa_circ_317527,RMVar_hsa_circ_208518,RMVar_hsa_circ_208523,RMVar_hsa_circ_280579,RMVar_hsa_circ_299925,RMVar_hsa_circ_208524,RMVar_hsa_circ_208525,RMVar_hsa_circ_272850 21668 RMVar_ID_21668 Human_SNP_ID_672030310 A-to-I Human chr20 + 3912865 3912865 3912865 CCAGGTACTTGGGAGGCTGAGGCAGGAGAATCACTTGAACCCTGGAGGTGGAGGGTGCGGTGAGC CCAGGTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCTGGAGGTGGAGGGTGCGGTGAGC A G PANK2 Ensembl:ENSG00000125779 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs755744146 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571351 RMVar_hsa_circ_208517,RMVar_hsa_circ_15339,RMVar_hsa_circ_287845,RMVar_hsa_circ_317527,RMVar_hsa_circ_208518,RMVar_hsa_circ_208523,RMVar_hsa_circ_280579,RMVar_hsa_circ_299925,RMVar_hsa_circ_208524,RMVar_hsa_circ_208525,RMVar_hsa_circ_272850 21669 RMVar_ID_21669 Human_SNP_ID_672030791 A-to-I Human chr20 + 3913918 3913918 3913918 TCATGCCATTCTTCTGCTTCAGCCTTCCAAGTAGCTGGGACTACAGGTGCCTGCCACCACGCCCG TCATGCCATTCTTCTGCTTCAGCCTTCCAAGTCGCTGGGACTACAGGTGCCTGCCACCACGCCCG A C PANK2 Ensembl:ENSG00000125779 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1248979056 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_208517,RMVar_hsa_circ_15339,RMVar_hsa_circ_287845,RMVar_hsa_circ_317527,RMVar_hsa_circ_208518,RMVar_hsa_circ_208523,RMVar_hsa_circ_280579,RMVar_hsa_circ_299925,RMVar_hsa_circ_208524,RMVar_hsa_circ_208525,RMVar_hsa_circ_272850 21670 RMVar_ID_21670 Human_SNP_ID_672030792 A-to-I Human chr20 + 3913918 3913918 3913918 TCATGCCATTCTTCTGCTTCAGCCTTCCAAGTAGCTGGGACTACAGGTGCCTGCCACCACGCCCG TCATGCCATTCTTCTGCTTCAGCCTTCCAAGTGGCTGGGACTACAGGTGCCTGCCACCACGCCCG A G PANK2 Ensembl:ENSG00000125779 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1248979056 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_208517,RMVar_hsa_circ_15339,RMVar_hsa_circ_287845,RMVar_hsa_circ_317527,RMVar_hsa_circ_208518,RMVar_hsa_circ_208523,RMVar_hsa_circ_280579,RMVar_hsa_circ_299925,RMVar_hsa_circ_208524,RMVar_hsa_circ_208525,RMVar_hsa_circ_272850 21671 RMVar_ID_21671 Human_SNP_ID_672032361 A-to-I Human chr20 + 3919180 3919180 3919180 GTGATCTGCCAGCCTCAGCCTCCCAAAGTTCCAGGATTACAGGTGTGAACCACTGTGCCTGAACT GTGATCTGCCAGCCTCAGCCTCCCAAAGTTCCCGGATTACAGGTGTGAACCACTGTGCCTGAACT A C PANK2 Ensembl:ENSG00000125779 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1257717338 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7001192 21672 RMVar_ID_21672 Human_SNP_ID_672032365 A-to-I Human chr20 + 3919186 3919186 3919186 TGCCAGCCTCAGCCTCCCAAAGTTCCAGGATTACAGGTGTGAACCACTGTGCCTGAACTTTTTTG TGCCAGCCTCAGCCTCCCAAAGTTCCAGGATTGCAGGTGTGAACCACTGTGCCTGAACTTTTTTG A G PANK2 Ensembl:ENSG00000125779 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1468678034 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7001192 21673 RMVar_ID_21673 Human_SNP_ID_672032628 A-to-I Human chr20 + 3920354 3920354 3920354 CATGGTCAATGTGGCAAAACCCTGTCTCTACTAAAAATACAAAAATTAGCTGGGCGCAATGGCGG CATGGTCAATGTGGCAAAACCCTGTCTCTACTGAAAATACAAAAATTAGCTGGGCGCAATGGCGG A G PANK2 Ensembl:ENSG00000125779 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1384946468 Functional Loss SNV dbSNP153 33..33 33 - - - 21674 RMVar_ID_21674 Human_SNP_ID_672034013 A-to-I Human chr20 + 3925303 3925303 3925303 GTCACCCAGGTGGAGTGCAGTGGGGCGATCTCAGCTCACTGCAACCTCTGCCTTCCAGGCTCAAG GTCACCCAGGTGGAGTGCAGTGGGGCGATCTCCGCTCACTGCAACCTCTGCCTTCCAGGCTCAAG A C PANK2 Ensembl:ENSG00000125779 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs557929549 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_682074 21675 RMVar_ID_21675 Human_SNP_ID_672034014 A-to-I Human chr20 + 3925303 3925303 3925303 GTCACCCAGGTGGAGTGCAGTGGGGCGATCTCAGCTCACTGCAACCTCTGCCTTCCAGGCTCAAG GTCACCCAGGTGGAGTGCAGTGGGGCGATCTCGGCTCACTGCAACCTCTGCCTTCCAGGCTCAAG A G PANK2 Ensembl:ENSG00000125779 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs557929549 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_682074 21676 RMVar_ID_21676 Human_SNP_ID_672034015 A-to-I Human chr20 + 3925303 3925303 3925303 GTCACCCAGGTGGAGTGCAGTGGGGCGATCTCAGCTCACTGCAACCTCTGCCTTCCAGGCTCAAG GTCACCCAGGTGGAGTGCAGTGGGGCGATCTCTGCTCACTGCAACCTCTGCCTTCCAGGCTCAAG A T PANK2 Ensembl:ENSG00000125779 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs557929549 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_682074 21677 RMVar_ID_21677 Human_SNP_ID_672034394 A-to-I Human chr20 + 3926662 3926662 3926662 GAGGAAACAGGCTCAGTTCCACTACTTTGGCCAGGTGCAATGGCTCATGCCTGTAATCCCAGCAC GAGGAAACAGGCTCAGTTCCACTACTTTGGCCGGGTGCAATGGCTCATGCCTGTAATCCCAGCAC A G PANK2 Ensembl:ENSG00000125779 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388977789 Functional Loss SNV dbSNP153 33..33 33 - - - 21678 RMVar_ID_21678 Human_SNP_ID_672034458 A-to-I Human chr20 + 3926822 3926822 3926822 ATAATTAGCCGGGAATGGTGGTGCGTGCCTGTAATCCCAGGTACTCGAGAGGCTGAGGCAGACAG ATAATTAGCCGGGAATGGTGGTGCGTGCCTGTGATCCCAGGTACTCGAGAGGCTGAGGCAGACAG A G PANK2 Ensembl:ENSG00000125779 Protein coding 3'UTR GSE100210;GSE107867;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;Bronchiolar epithelium,BEP2D cell line - 29129909,30559470,30559470,31158229 RNA-Seq:(High) rs1480663498 Functional Loss SNV dbSNP153 33..33 33 - - - 21679 RMVar_ID_21679 Human_SNP_ID_672034459 A-to-I Human chr20 + 3926822 3926822 3926822 ATAATTAGCCGGGAATGGTGGTGCGTGCCTGTAATCCCAGGTACTCGAGAGGCTGAGGCAGACAG ATAATTAGCCGGGAATGGTGGTGCGTGCCTGTTATCCCAGGTACTCGAGAGGCTGAGGCAGACAG A T PANK2 Ensembl:ENSG00000125779 Protein coding 3'UTR GSE100210;GSE107867;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;Bronchiolar epithelium,BEP2D cell line - 29129909,30559470,30559470,31158229 RNA-Seq:(High) rs1480663498 Functional Loss SNV dbSNP153 33..33 33 - - - 21680 RMVar_ID_21680 Human_SNP_ID_672034495 A-to-I Human chr20 + 3926927 3926927 3926927 AGATTGCTGCACTGCACTCCAGCCTGGGTGACAGCAAGACTGTCTCAAAAAAAAAAAAAAAAAAA AGATTGCTGCACTGCACTCCAGCCTGGGTGACCGCAAGACTGTCTCAAAAAAAAAAAAAAAAAAA A C PANK2 Ensembl:ENSG00000125779 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1440035292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23905293 21681 RMVar_ID_21681 Human_SNP_ID_672034496 A-to-I Human chr20 + 3926927 3926927 3926927 AGATTGCTGCACTGCACTCCAGCCTGGGTGACAGCAAGACTGTCTCAAAAAAAAAAAAAAAAAAA AGATTGCTGCACTGCACTCCAGCCTGGGTGACGGCAAGACTGTCTCAAAAAAAAAAAAAAAAAAA A G PANK2 Ensembl:ENSG00000125779 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1440035292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23905293 21682 RMVar_ID_21682 Human_SNP_ID_672035026 A-to-I Human chr20 - 3928672 3928672 3928672 ACGATCTTGGCCCACTGCAAGCTCCGCCTCCCAGGTTCACGCCATTCTCCCGCCTCGGGAGCTGG ACGATCTTGGCCCACTGCAAGCTCCGCCTCCCCGGTTCACGCCATTCTCCCGCCTCGGGAGCTGG T G RNF24 Ensembl:ENSG00000101236 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1169123961 Functional Loss SNV dbSNP153 33..33 33 - - - 21683 RMVar_ID_21683 Human_SNP_ID_672035136 A-to-I Human chr20 + 3928872 3928872 3928872 AAGCATTTTCTTTTCTTGTGTGTTTTTTTGAGACGGAGTCTCGCTCTGTTGCCCAGGCTGGAGTG AAGCATTTTCTTTTCTTGTGTGTTTTTTTGAGGCGGAGTCTCGCTCTGTTGCCCAGGCTGGAGTG A G PANK2 Ensembl:ENSG00000125779 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053177160 Functional Loss SNV dbSNP153 33..33 33 - - - 21684 RMVar_ID_21684 Human_SNP_ID_672035161 A-to-I Human chr20 - 3928934 3928934 3928934 TGGGACAGGAGAATTGATTGAACCCGGGAGACAGAAGTTGCAGTGAGCCAAGATCCCCACTGCAC TGGGACAGGAGAATTGATTGAACCCGGGAGACGGAAGTTGCAGTGAGCCAAGATCCCCACTGCAC T C RNF24 Ensembl:ENSG00000101236 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1375468611 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14107379,Human_RBP_ID_17571805 21685 RMVar_ID_21685 Human_SNP_ID_672035166 A-to-I Human chr20 - 3928945 3928945 3928945 ACTCAGGAGGCTGGGACAGGAGAATTGATTGAACCCGGGAGACAGAAGTTGCAGTGAGCCAAGAT ACTCAGGAGGCTGGGACAGGAGAATTGATTGAGCCCGGGAGACAGAAGTTGCAGTGAGCCAAGAT T C RNF24 Ensembl:ENSG00000101236 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1180909107 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14107379,Human_RBP_ID_17571805 21686 RMVar_ID_21686 Human_SNP_ID_672035190 A-to-I Human chr20 - 3929016 3929016 3929016 ATGGTGAAACCCCCTCTACTAAAAATACAAAAATTTGCCGGGTGTGGTGACGCATGCCTGTAATC ATGGTGAAACCCCCTCTACTAAAAATACAAAAGTTTGCCGGGTGTGGTGACGCATGCCTGTAATC T C RNF24 Ensembl:ENSG00000101236 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs372312953 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17971796 21687 RMVar_ID_21687 Human_SNP_ID_672035201 A-to-I Human chr20 + 3929049 3929049 3929049 TTTTGTATTTTTAGTAGAGGGGGTTTCACCATATTGGTCAGGCTGGTCTTGAACTCTTGACCTAA TTTTGTATTTTTAGTAGAGGGGGTTTCACCATGTTGGTCAGGCTGGTCTTGAACTCTTGACCTAA A G PANK2 Ensembl:ENSG00000125779 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 29129909,30559470 RNA-Seq:(High) rs1238306271 Functional Loss SNV dbSNP153 33..33 33 - - - 21688 RMVar_ID_21688 Human_SNP_ID_672035202 A-to-I Human chr20 + 3929049 3929049 3929049 TTTTGTATTTTTAGTAGAGGGGGTTTCACCATATTGGTCAGGCTGGTCTTGAACTCTTGACCTAA TTTTGTATTTTTAGTAGAGGGGGTTTCACCATTTTGGTCAGGCTGGTCTTGAACTCTTGACCTAA A T PANK2 Ensembl:ENSG00000125779 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 29129909,30559470 RNA-Seq:(High) rs1238306271 Functional Loss SNV dbSNP153 33..33 33 - - - 21689 RMVar_ID_21689 Human_SNP_ID_672035207 A-to-I Human chr20 - 3929074 3929072 3929074 GGGAGGCCGAGGCAGGCGGATCACCTTAGGTCAAGAGTTCAAGACCAGCCTGACCAATATGGTGA GGGAGGCCGAGGCAGGCGGATCACCTTAGGTC__GAGTTCAAGACCAGCCTGACCAATATGGTGA CTT C RNF24 Ensembl:ENSG00000101236 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1311705717 Functional Loss DEL dbSNP153 33..34 33 - - - 21690 RMVar_ID_21690 Human_SNP_ID_672035213 A-to-I Human chr20 - 3929114 3929114 3929114 GCGATGGCTCACGCCTGTAATCCCAACATCCCAGCACTTTGGGAGGCCGAGGCAGGCGGATCACC GCGATGGCTCACGCCTGTAATCCCAACATCCCTGCACTTTGGGAGGCCGAGGCAGGCGGATCACC T A RNF24 Ensembl:ENSG00000101236 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1176963406 Functional Loss SNV dbSNP153 33..33 33 - - - 21691 RMVar_ID_21691 Human_SNP_ID_672035299 A-to-I Human chr20 - 3929317 3929317 3929317 GTAGCTCACTGCAGCCTCAACTTCCTGGACTCAAGTGATCCTCCCGCCTCAGTCTGTAGCTGCGT GTAGCTCACTGCAGCCTCAACTTCCTGGACTCGAGTGATCCTCCCGCCTCAGTCTGTAGCTGCGT T C RNF24 Ensembl:ENSG00000101236 Protein coding 3'UTR GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 29129909,30559470 RNA-Seq:(High) rs1269121944 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571177 21692 RMVar_ID_21692 Human_SNP_ID_672042805 A-to-I Human chr20 - 3962294 3962294 3962294 GTTGGAGTGCAGTGGCACAGTCTCTGCTCACTACAGCTTTCCTCCTAGGCTCAAGTGATCCTCCC GTTGGAGTGCAGTGGCACAGTCTCTGCTCACTGCAGCTTTCCTCCTAGGCTCAAGTGATCCTCCC T C RNF24 Ensembl:ENSG00000101236 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1165597752 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_208526,RMVar_hsa_circ_280870,RMVar_hsa_circ_296842,RMVar_hsa_circ_208527,RMVar_hsa_circ_208529,RMVar_hsa_circ_208531,RMVar_hsa_circ_274265,RMVar_hsa_circ_287625,RMVar_hsa_circ_122559,RMVar_hsa_circ_208530,RMVar_hsa_circ_208533,RMVar_hsa_circ_328639,RMVar_hsa_circ_208528,RMVar_hsa_circ_278180,RMVar_hsa_circ_208532 21693 RMVar_ID_21693 Human_SNP_ID_672042939 A-to-I Human chr20 - 3962787 3962787 3962787 AGAATCCCTTGAACCCGGGAGGGAGAGATTGCAGTGAGCCAAGATCGTGCCATTGCAGTCCAGCC AGAATCCCTTGAACCCGGGAGGGAGAGATTGCTGTGAGCCAAGATCGTGCCATTGCAGTCCAGCC T A RNF24 Ensembl:ENSG00000101236 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1294506879 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_208526,RMVar_hsa_circ_280870,RMVar_hsa_circ_296842,RMVar_hsa_circ_208527,RMVar_hsa_circ_208529,RMVar_hsa_circ_208531,RMVar_hsa_circ_274265,RMVar_hsa_circ_287625,RMVar_hsa_circ_122559,RMVar_hsa_circ_208530,RMVar_hsa_circ_208533,RMVar_hsa_circ_328639,RMVar_hsa_circ_208528,RMVar_hsa_circ_278180,RMVar_hsa_circ_208532 21694 RMVar_ID_21694 Human_SNP_ID_672043058 A-to-I Human chr20 - 3963394 3963394 3963394 AAGGTCGGGAGTTCTCGACCAGCCTGGCCAACATGGTGGAACTCCGTCTCTACCAAAAATACAAA AAGGTCGGGAGTTCTCGACCAGCCTGGCCAACGTGGTGGAACTCCGTCTCTACCAAAAATACAAA T C RNF24 Ensembl:ENSG00000101236 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1405534970 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_208526,RMVar_hsa_circ_280870,RMVar_hsa_circ_296842,RMVar_hsa_circ_208527,RMVar_hsa_circ_208529,RMVar_hsa_circ_208531,RMVar_hsa_circ_274265,RMVar_hsa_circ_287625,RMVar_hsa_circ_122559,RMVar_hsa_circ_208530,RMVar_hsa_circ_208533,RMVar_hsa_circ_328639,RMVar_hsa_circ_208528,RMVar_hsa_circ_278180,RMVar_hsa_circ_208532 21695 RMVar_ID_21695 Human_SNP_ID_672043643 A-to-I Human chr20 - 3966012 3966012 3966012 CCCCTGCATTAGCCTCCTGAGTAGCTGGGATTACAAGTGTGTGCCACCACGCCCAGTTAATTTTT CCCCTGCATTAGCCTCCTGAGTAGCTGGGATTGCAAGTGTGTGCCACCACGCCCAGTTAATTTTT T C RNF24 Ensembl:ENSG00000101236 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1226904881 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_296842,RMVar_hsa_circ_208527,RMVar_hsa_circ_114672,RMVar_hsa_circ_208529,RMVar_hsa_circ_274265,RMVar_hsa_circ_122559,RMVar_hsa_circ_208530,RMVar_hsa_circ_208533,RMVar_hsa_circ_328639,RMVar_hsa_circ_208528,RMVar_hsa_circ_299943,RMVar_hsa_circ_208535,RMVar_hsa_circ_208536 21696 RMVar_ID_21696 Human_SNP_ID_672044309 A-to-I Human chr20 - 3968577 3968577 3968577 GTCTTGCTTTGTCACCCAGGCTGGAGCGTAGCAGTGATATCATAGCTCACTGTAACCTTGAATTC GTCTTGCTTTGTCACCCAGGCTGGAGCGTAGCGGTGATATCATAGCTCACTGTAACCTTGAATTC T C RNF24 Ensembl:ENSG00000101236 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1454484845 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_296842,RMVar_hsa_circ_208527,RMVar_hsa_circ_114672,RMVar_hsa_circ_208529,RMVar_hsa_circ_274265,RMVar_hsa_circ_122559,RMVar_hsa_circ_208530,RMVar_hsa_circ_208533,RMVar_hsa_circ_328639,RMVar_hsa_circ_208528,RMVar_hsa_circ_299943,RMVar_hsa_circ_208535,RMVar_hsa_circ_208536 21697 RMVar_ID_21697 Human_SNP_ID_672051026 A-to-I Human chr20 - 3997625 3997624 3997626 GCCCAGGGGTTTGAGAGCAGCCTGGGAAACATAGGGAAACCCCATCTGTGGAAAAAAAAAATAAT GCCCAGGGGTTTGAGAGCAGCCTGGGAAACA__GGGAAACCCCATCTGTGGAAAAAAAAAATAAT CTA C RNF24 Ensembl:ENSG00000101236 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1443064967 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_114672,RMVar_hsa_circ_122559,RMVar_hsa_circ_208528,RMVar_hsa_circ_208536 21698 RMVar_ID_21698 Human_SNP_ID_672089328 A-to-I Human chr20 + 4143308 4143306 4143308 TGTGTGTATATTACACACACAATATACTGTGTATATATATACGCACACACACACGATATTGTGTA TGTGTGTATATTACACACACAATATACTGTG__TATATATACGCACACACACACGATATTGTGTA GTA G SMOX Ensembl:ENSG00000088826 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs765048887 Functional Loss DEL dbSNP153 32..33 33 - - - 21699 RMVar_ID_21699 Human_SNP_ID_672292617 A-to-I Human chr20 - 4968830 4968830 4968830 CCTGTATTGCTAGCTACTCTGGAGGCTGAGGCAGGAGAATTGCATGACCTCAGGAGGCTGAGGTT CCTGTATTGCTAGCTACTCTGGAGGCTGAGGCGGGAGAATTGCATGACCTCAGGAGGCTGAGGTT T C SLC23A2 Ensembl:ENSG00000089057 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027961739 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123079,RMVar_hsa_circ_208555,RMVar_hsa_circ_124520,RMVar_hsa_circ_208561,RMVar_hsa_circ_331565,RMVar_hsa_circ_367961,RMVar_hsa_circ_208568,RMVar_hsa_circ_327039,RMVar_hsa_circ_349556,RMVar_hsa_circ_208570 21700 RMVar_ID_21700 Human_SNP_ID_672298539 A-to-I Human chr20 - 4991205 4991205 4991205 ACTAGGGAGGCTGATTGTGGGAAGAGAACTCAAGCCCAGGAGTTCAAGGCTGCAGTGAGTTGTGA ACTAGGGAGGCTGATTGTGGGAAGAGAACTCACGCCCAGGAGTTCAAGGCTGCAGTGAGTTGTGA T G SLC23A2 Ensembl:ENSG00000089057 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1380244120 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123079,RMVar_hsa_circ_208555,RMVar_hsa_circ_124520,RMVar_hsa_circ_208561 21701 RMVar_ID_21701 Human_SNP_ID_672318879 A-to-I Human chr20 - 5064960 5064960 5064960 ACTTTGTTGGCCCAGGCTGGTCTCAAACTCCTAAGCTCAAGTGATCTTCCCACCTTGGTCTCCCA ACTTTGTTGGCCCAGGCTGGTCTCAAACTCCTTAGCTCAAGTGATCTTCCCACCTTGGTCTCCCA T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1478813083 Functional Loss SNV dbSNP153 33..33 33 - - - 21702 RMVar_ID_21702 Human_SNP_ID_672324311 A-to-I Human chr20 - 5086737 5086737 5086737 TGTGATTGTGCCACTGTACTCCACTCTGAGCAACAGAGCAAGACCCTACCTCAAAAAAAAAAAGA TGTGATTGTGCCACTGTACTCCACTCTGAGCAGCAGAGCAAGACCCTACCTCAAAAAAAAAAAGA T C TMEM230 Ensembl:ENSG00000089063 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1439803354 Functional Loss SNV dbSNP153 33..33 33 - - - 21703 RMVar_ID_21703 Human_SNP_ID_672324312 A-to-I Human chr20 - 5086737 5086737 5086737 TGTGATTGTGCCACTGTACTCCACTCTGAGCAACAGAGCAAGACCCTACCTCAAAAAAAAAAAGA TGTGATTGTGCCACTGTACTCCACTCTGAGCACCAGAGCAAGACCCTACCTCAAAAAAAAAAAGA T G TMEM230 Ensembl:ENSG00000089063 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1439803354 Functional Loss SNV dbSNP153 33..33 33 - - - 21704 RMVar_ID_21704 Human_SNP_ID_672324313 A-to-I Human chr20 - 5086738 5086738 5086738 TTGTGATTGTGCCACTGTACTCCACTCTGAGCAACAGAGCAAGACCCTACCTCAAAAAAAAAAAG TTGTGATTGTGCCACTGTACTCCACTCTGAGCGACAGAGCAAGACCCTACCTCAAAAAAAAAAAG T C TMEM230 Ensembl:ENSG00000089063 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs942790365 Functional Loss SNV dbSNP153 33..33 33 - - - 21705 RMVar_ID_21705 Human_SNP_ID_672328206 A-to-I Human chr20 - 5101549 5101549 5101549 AGGTATGGTGACTGACACCTGTAACTCCAGCTACTTGGAGGCTGAGGTGGGAGGATCACTTGAGC AGGTATGGTGACTGACACCTGTAACTCCAGCTGCTTGGAGGCTGAGGTGGGAGGATCACTTGAGC T C TMEM230 Ensembl:ENSG00000089063 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1363464295 Functional Loss SNV dbSNP153 33..33 33 - - - 21706 RMVar_ID_21706 Human_SNP_ID_672329286 A-to-I Human chr20 - 5105504 5105504 5105504 TAACTGCAACCTCCGCCTCCCAGGTTCATGCTATTCTTGTGCCTCAGCCTCCCGAGTAGCTGGAA TAACTGCAACCTCCGCCTCCCAGGTTCATGCTCTTCTTGTGCCTCAGCCTCCCGAGTAGCTGGAA T G TMEM230 Ensembl:ENSG00000089063 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs995779679 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14141810 21707 RMVar_ID_21707 Human_SNP_ID_672330000 A-to-I Human chr20 - 5107894 5107894 5107894 TTGGCCAGGCTGGTCTCGAACTCTTAACCTCCAGTGATTCACCCACTTCGGCCTCCCAAAGCGCT TTGGCCAGGCTGGTCTCGAACTCTTAACCTCCGGTGATTCACCCACTTCGGCCTCCCAAAGCGCT T C TMEM230 Ensembl:ENSG00000089063 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs774024420 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14141855 RMVar_hsa_circ_270115,RMVar_hsa_circ_345358,RMVar_hsa_circ_208574 21708 RMVar_ID_21708 Human_SNP_ID_672330036 A-to-I Human chr20 - 5108031 5108031 5108031 CTGGCTCACTGCAACCTCCCCCTCCTGGTTCAAGTGATTCTTGTACCTCAGCCTCCCTAGTAGCT CTGGCTCACTGCAACCTCCCCCTCCTGGTTCAGGTGATTCTTGTACCTCAGCCTCCCTAGTAGCT T C TMEM230 Ensembl:ENSG00000089063 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474608146 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_270115,RMVar_hsa_circ_345358,RMVar_hsa_circ_208574 21709 RMVar_ID_21709 Human_SNP_ID_672330843 A-to-I Human chr20 - 5111047 5111047 5111047 CTTCCAAATAGCTGGGATTACAGGTGTGTGCCACTGCACCTGGCTAATTTTTGTAGTTTTAGTAG CTTCCAAATAGCTGGGATTACAGGTGTGTGCCGCTGCACCTGGCTAATTTTTGTAGTTTTAGTAG T C TMEM230 Ensembl:ENSG00000089063 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1000607863 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76255,RMVar_hsa_circ_345358,RMVar_hsa_circ_208575 21710 RMVar_ID_21710 Human_SNP_ID_672330968 A-to-I Human chr20 - 5111446 5111446 5111446 CACCACCATGCCCGGCTAATTTTTGTATTTCTAGTAGAGACAGGGTTTCCCCATATTGGCCAGGC CACCACCATGCCCGGCTAATTTTTGTATTTCTGGTAGAGACAGGGTTTCCCCATATTGGCCAGGC T C TMEM230 Ensembl:ENSG00000089063 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs567482407 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76255,RMVar_hsa_circ_345358,RMVar_hsa_circ_208575 21711 RMVar_ID_21711 Human_SNP_ID_672331022 A-to-I Human chr20 - 5111596 5111596 5111596 TTTTTTTTTTTTTTTTTTTTTAGATGGAGTCTAGTTCTGTCGCCCAGGCTGGAGCCCAGTGGTGT TTTTTTTTTTTTTTTTTTTTTAGATGGAGTCTGGTTCTGTCGCCCAGGCTGGAGCCCAGTGGTGT T C TMEM230 Ensembl:ENSG00000089063 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs745443202 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14141947,Human_RBP_ID_25621022 Human_Splice_Rec_2057898,Human_Splice_Rec_2057899,Human_Splice_Rec_2057922,Human_Splice_Rec_2057923 RMVar_hsa_circ_76255,RMVar_hsa_circ_345358,RMVar_hsa_circ_208575 21712 RMVar_ID_21712 Human_SNP_ID_672331023 A-to-I Human chr20 - 5111596 5111596 5111596 TTTTTTTTTTTTTTTTTTTTTAGATGGAGTCTAGTTCTGTCGCCCAGGCTGGAGCCCAGTGGTGT TTTTTTTTTTTTTTTTTTTTTAGATGGAGTCTCGTTCTGTCGCCCAGGCTGGAGCCCAGTGGTGT T G TMEM230 Ensembl:ENSG00000089063 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs745443202 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14141947,Human_RBP_ID_25621022 Human_Splice_Rec_2057898,Human_Splice_Rec_2057899,Human_Splice_Rec_2057922,Human_Splice_Rec_2057923 RMVar_hsa_circ_76255,RMVar_hsa_circ_345358,RMVar_hsa_circ_208575 21713 RMVar_ID_21713 Human_SNP_ID_672331216 A-to-I Human chr20 - 5112026 5112026 5112026 GCCTGGCCAATATGGTGAAGCCCGTCTCTACTAAAAATAGAAAAATTAGCCGGGCGTGGTAGCAG GCCTGGCCAATATGGTGAAGCCCGTCTCTACTGAAAATAGAAAAATTAGCCGGGCGTGGTAGCAG T C TMEM230 Ensembl:ENSG00000089063 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1317554432 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10028207,Human_RBP_ID_25631429 RMVar_hsa_circ_76255,RMVar_hsa_circ_208575 21714 RMVar_ID_21714 Human_SNP_ID_672336446 A-to-I Human chr20 + 5130823 5130823 5130823 AGAAAAGAAAAGCTCTGGAGGCTGGGCGTGGTAGCTCACGCCTGTAATCCCAGCACTTTGGGAGG AGAAAAGAAAAGCTCTGGAGGCTGGGCGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGG A G CDS2 Ensembl:ENSG00000101290 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs556987055 Functional Loss SNV dbSNP153 33..33 33 - - - 21715 RMVar_ID_21715 Human_SNP_ID_672337212 A-to-I Human chr20 + 5133786 5133786 5133786 ACCTCAGGTGATACTCCCGCCTTGGCCTACCAAAGTGATGGGATTACAGGCGTGAGCCACCGCGC ACCTCAGGTGATACTCCCGCCTTGGCCTACCAGAGTGATGGGATTACAGGCGTGAGCCACCGCGC A G CDS2 Ensembl:ENSG00000101290 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs531837119 Functional Loss SNV dbSNP153 33..33 33 - - - 21716 RMVar_ID_21716 Human_SNP_ID_672338741 A-to-I Human chr20 + 5139195 5139195 5139195 GAAACCTCATCTTTGCTAAAAGTACAAAAATTAGCCCGGTGTGGGAGCCTGCACCTGTAATCCTA GAAACCTCATCTTTGCTAAAAGTACAAAAATTGGCCCGGTGTGGGAGCCTGCACCTGTAATCCTA A G CDS2 Ensembl:ENSG00000101290 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs977947533 Functional Loss SNV dbSNP153 33..33 33 - - - 21717 RMVar_ID_21717 Human_SNP_ID_672351169 A-to-I Human chr20 + 5190372 5190372 5190372 TCTTTTTTTTTTTTTTTTGGAGGGTATTTTTTATTTGTGGGTTCAAAAAATCTGTATATACAGTC TCTTTTTTTTTTTTTTTTGGAGGGTATTTTTTTTTTGTGGGTTCAAAAAATCTGTATATACAGTC A T CDS2 Ensembl:ENSG00000101290 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs879006229 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_566680,Human_RBP_ID_3651551,Human_RBP_ID_7013318,Human_RBP_ID_14143758,Human_RBP_ID_20668552,Human_RBP_ID_22395355,Human_RBP_ID_24424427,Human_RBP_ID_24492311,Human_RBP_ID_27703135 Human_miRNA_ID_855187 RMVar_hsa_circ_208596,RMVar_hsa_circ_119062,RMVar_hsa_circ_208598 21718 RMVar_ID_21718 Human_SNP_ID_672352335 A-to-I Human chr20 + 5195158 5195158 5195158 TGGTTGTGAGGATATAACGAGGTAATGCATGTAAGCATTTAGTACCATGCCTGGCACATAGTAAG TGGTTGTGAGGATATAACGAGGTAATGCATGTGAGCATTTAGTACCATGCCTGGCACATAGTAAG A G CDS2 Ensembl:ENSG00000101290 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs111535554 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4653366 RMVar_hsa_circ_208596,RMVar_hsa_circ_119062 21719 RMVar_ID_21719 Human_SNP_ID_672356704 A-to-I Human chr20 + 5211726 5211726 5211726 TTTTAAGGCTTGTAGAGACAAGCTTTTGCCATATTGCTTAGGCTGGTTTTGAACTCCTGGCCTCA TTTTAAGGCTTGTAGAGACAAGCTTTTGCCATGTTGCTTAGGCTGGTTTTGAACTCCTGGCCTCA A G lnc-CDS2-3 RNACentral:URS00008B9C7C lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs922645582 Functional Loss SNV dbSNP153 33..33 33 - - - 21720 RMVar_ID_21720 Human_SNP_ID_672442058 A-to-I Human chr20 - 5555395 5555395 5555395 AGCTGGGACTGCAGGCATGCACAACCACATCCAGCTAATTTTTGTATTTTTGGTAGAGACAGGGT AGCTGGGACTGCAGGCATGCACAACCACATCCTGCTAATTTTTGTATTTTTGGTAGAGACAGGGT T A GPCPD1 Ensembl:ENSG00000125772 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs578028026 Functional Loss SNV dbSNP153 33..33 33 - - - 21721 RMVar_ID_21721 Human_SNP_ID_672442059 A-to-I Human chr20 - 5555395 5555395 5555395 AGCTGGGACTGCAGGCATGCACAACCACATCCAGCTAATTTTTGTATTTTTGGTAGAGACAGGGT AGCTGGGACTGCAGGCATGCACAACCACATCCGGCTAATTTTTGTATTTTTGGTAGAGACAGGGT T C GPCPD1 Ensembl:ENSG00000125772 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs578028026 Functional Loss SNV dbSNP153 33..33 33 - - - 21722 RMVar_ID_21722 Human_SNP_ID_672442175 A-to-I Human chr20 - 5555815 5555815 5555815 AGTCTCACTCTTAATACCCTGGCTGGAGTGCAATGGCATGATCTTGGCTCACTGCAACCTCCATC AGTCTCACTCTTAATACCCTGGCTGGAGTGCAGTGGCATGATCTTGGCTCACTGCAACCTCCATC T C GPCPD1 Ensembl:ENSG00000125772 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs557087903 Functional Loss SNV dbSNP153 33..33 33 - - - 21723 RMVar_ID_21723 Human_SNP_ID_672446188 A-to-I Human chr20 - 5572167 5572167 5572167 TCACCCAGGCTGGAGTGCAGTGGCAGGATCATAGCTCACTATAGCCTCAACCTCCTGGGCTCAAA TCACCCAGGCTGGAGTGCAGTGGCAGGATCATGGCTCACTATAGCCTCAACCTCCTGGGCTCAAA T C GPCPD1 Ensembl:ENSG00000125772 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1192131555 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_53234,RMVar_hsa_circ_305105,RMVar_hsa_circ_330101,RMVar_hsa_circ_304782,RMVar_hsa_circ_55727,RMVar_hsa_circ_47276,RMVar_hsa_circ_46097,RMVar_hsa_circ_208603,RMVar_hsa_circ_208604,RMVar_hsa_circ_47274,RMVar_hsa_circ_62086,RMVar_hsa_circ_337741,RMVar_hsa_circ_351747,RMVar_hsa_circ_368063,RMVar_hsa_circ_317545,RMVar_hsa_circ_68771,RMVar_hsa_circ_52985,RMVar_hsa_circ_208610,RMVar_hsa_circ_9944 21724 RMVar_ID_21724 Human_SNP_ID_672447477 A-to-I Human chr20 - 5577203 5577203 5577203 AAAATTAGCCAGGCGTGTTGGCGCGTGACTGTAATCCCAGCTACTCGAGAGGCTGAGGCAGGAGA AAAATTAGCCAGGCGTGTTGGCGCGTGACTGTGATCCCAGCTACTCGAGAGGCTGAGGCAGGAGA T C GPCPD1 Ensembl:ENSG00000125772 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1197078169 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5768,RMVar_hsa_circ_53234,RMVar_hsa_circ_305105,RMVar_hsa_circ_330101,RMVar_hsa_circ_304782,RMVar_hsa_circ_55727,RMVar_hsa_circ_47276,RMVar_hsa_circ_46097,RMVar_hsa_circ_208603,RMVar_hsa_circ_208604,RMVar_hsa_circ_62086,RMVar_hsa_circ_337741,RMVar_hsa_circ_368063,RMVar_hsa_circ_317545,RMVar_hsa_circ_52985,RMVar_hsa_circ_208610,RMVar_hsa_circ_284624,RMVar_hsa_circ_2151,RMVar_hsa_circ_362338,RMVar_hsa_circ_112779,RMVar_hsa_circ_74360,RMVar_hsa_circ_208612 21725 RMVar_ID_21725 Human_SNP_ID_672448552 A-to-I Human chr20 - 5581006 5581006 5581006 GTCAGCTGGGCATGGTGGGCGCCTATAATCCCAGCTACTTGGGAGGCTGAGGCATGAGAATCTCT GTCAGCTGGGCATGGTGGGCGCCTATAATCCCGGCTACTTGGGAGGCTGAGGCATGAGAATCTCT T C GPCPD1 Ensembl:ENSG00000125772 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs908111523 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5768,RMVar_hsa_circ_305105,RMVar_hsa_circ_330101,RMVar_hsa_circ_304782,RMVar_hsa_circ_46097,RMVar_hsa_circ_208603,RMVar_hsa_circ_208604,RMVar_hsa_circ_62086,RMVar_hsa_circ_337741,RMVar_hsa_circ_368063,RMVar_hsa_circ_317545,RMVar_hsa_circ_52985,RMVar_hsa_circ_208610,RMVar_hsa_circ_284624,RMVar_hsa_circ_2151,RMVar_hsa_circ_112779,RMVar_hsa_circ_3111,RMVar_hsa_circ_7694,RMVar_hsa_circ_343120,RMVar_hsa_circ_208612,RMVar_hsa_circ_305742,RMVar_hsa_circ_346212,RMVar_hsa_circ_25003 21726 RMVar_ID_21726 Human_SNP_ID_672448554 A-to-I Human chr20 - 5581014 5581014 5581014 AAATACAAGTCAGCTGGGCATGGTGGGCGCCTATAATCCCAGCTACTTGGGAGGCTGAGGCATGA AAATACAAGTCAGCTGGGCATGGTGGGCGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCATGA T C GPCPD1 Ensembl:ENSG00000125772 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1208005920 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5768,RMVar_hsa_circ_305105,RMVar_hsa_circ_330101,RMVar_hsa_circ_304782,RMVar_hsa_circ_46097,RMVar_hsa_circ_208603,RMVar_hsa_circ_208604,RMVar_hsa_circ_62086,RMVar_hsa_circ_337741,RMVar_hsa_circ_368063,RMVar_hsa_circ_317545,RMVar_hsa_circ_52985,RMVar_hsa_circ_208610,RMVar_hsa_circ_284624,RMVar_hsa_circ_2151,RMVar_hsa_circ_112779,RMVar_hsa_circ_3111,RMVar_hsa_circ_7694,RMVar_hsa_circ_343120,RMVar_hsa_circ_208612,RMVar_hsa_circ_305742,RMVar_hsa_circ_346212,RMVar_hsa_circ_25003 21727 RMVar_ID_21727 Human_SNP_ID_672448568 A-to-I Human chr20 - 5581073 5581073 5581073 CAGGAGTTTAGGAGTTTGAGACCAGCTTGGCCAGCATGGTGACACCCTGTCTCTACTAAAAATAC CAGGAGTTTAGGAGTTTGAGACCAGCTTGGCCGGCATGGTGACACCCTGTCTCTACTAAAAATAC T C GPCPD1 Ensembl:ENSG00000125772 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs937409654 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5768,RMVar_hsa_circ_305105,RMVar_hsa_circ_330101,RMVar_hsa_circ_304782,RMVar_hsa_circ_46097,RMVar_hsa_circ_208603,RMVar_hsa_circ_208604,RMVar_hsa_circ_62086,RMVar_hsa_circ_337741,RMVar_hsa_circ_368063,RMVar_hsa_circ_317545,RMVar_hsa_circ_52985,RMVar_hsa_circ_208610,RMVar_hsa_circ_284624,RMVar_hsa_circ_2151,RMVar_hsa_circ_112779,RMVar_hsa_circ_3111,RMVar_hsa_circ_7694,RMVar_hsa_circ_343120,RMVar_hsa_circ_208612,RMVar_hsa_circ_305742,RMVar_hsa_circ_346212,RMVar_hsa_circ_25003 21728 RMVar_ID_21728 Human_SNP_ID_672448582 A-to-I Human chr20 - 5581148 5581148 5581148 GTGGGCAGGGTGAGGTGGCTCATGCCTGTAATACCAGCACTTTGGGAGGCCTGAGGAAGGCAGAT GTGGGCAGGGTGAGGTGGCTCATGCCTGTAATTCCAGCACTTTGGGAGGCCTGAGGAAGGCAGAT T A GPCPD1 Ensembl:ENSG00000125772 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1399520235 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5768,RMVar_hsa_circ_305105,RMVar_hsa_circ_330101,RMVar_hsa_circ_304782,RMVar_hsa_circ_46097,RMVar_hsa_circ_208603,RMVar_hsa_circ_208604,RMVar_hsa_circ_62086,RMVar_hsa_circ_337741,RMVar_hsa_circ_368063,RMVar_hsa_circ_317545,RMVar_hsa_circ_52985,RMVar_hsa_circ_208610,RMVar_hsa_circ_284624,RMVar_hsa_circ_2151,RMVar_hsa_circ_112779,RMVar_hsa_circ_3111,RMVar_hsa_circ_7694,RMVar_hsa_circ_343120,RMVar_hsa_circ_208612,RMVar_hsa_circ_305742,RMVar_hsa_circ_346212,RMVar_hsa_circ_25003 21729 RMVar_ID_21729 Human_SNP_ID_672449510 A-to-I Human chr20 - 5584128 5584128 5584128 TTTGGTCAAAGACAGGCCACACGTGCAGCAGCAGTCTCATATGATTATAATGAAGCTGAAAAATT TTTGGTCAAAGACAGGCCACACGTGCAGCAGCGGTCTCATATGATTATAATGAAGCTGAAAAATT T C GPCPD1 Ensembl:ENSG00000125772 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6053517 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_1988,GWAS_ID_1989,GWAS_ID_1990,GWAS_ID_1991,GWAS_ID_1992,GWAS_ID_1993,GWAS_ID_1994,GWAS_ID_1995,GWAS_ID_1996,GWAS_ID_1997,GWAS_ID_1998,GWAS_ID_1999,GWAS_ID_2000 RMVar_hsa_circ_5768,RMVar_hsa_circ_305105,RMVar_hsa_circ_330101,RMVar_hsa_circ_304782,RMVar_hsa_circ_46097,RMVar_hsa_circ_208603,RMVar_hsa_circ_208604,RMVar_hsa_circ_62086,RMVar_hsa_circ_337741,RMVar_hsa_circ_368063,RMVar_hsa_circ_317545,RMVar_hsa_circ_52985,RMVar_hsa_circ_208610,RMVar_hsa_circ_284624,RMVar_hsa_circ_2151,RMVar_hsa_circ_112779,RMVar_hsa_circ_3111,RMVar_hsa_circ_7694,RMVar_hsa_circ_343120,RMVar_hsa_circ_208612,RMVar_hsa_circ_305742,RMVar_hsa_circ_346212,RMVar_hsa_circ_25003 21730 RMVar_ID_21730 Human_SNP_ID_672453189 A-to-I Human chr20 - 5599366 5599366 5599366 GCCTCCTGGGTTCAAGTGAATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCATCTG GCCTCCTGGGTTCAAGTGAATTCTCCTGCCTCGGCCTCCTGAGTAGCTGGGATTACAGGCATCTG T C GPCPD1 Ensembl:ENSG00000125772 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1331289025 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_304782,RMVar_hsa_circ_208603,RMVar_hsa_circ_317545,RMVar_hsa_circ_52985,RMVar_hsa_circ_284624,RMVar_hsa_circ_112779,RMVar_hsa_circ_7694,RMVar_hsa_circ_208612,RMVar_hsa_circ_346212,RMVar_hsa_circ_208615,RMVar_hsa_circ_95579,RMVar_hsa_circ_100167,RMVar_hsa_circ_208616,RMVar_hsa_circ_348006 21731 RMVar_ID_21731 Human_SNP_ID_672453245 A-to-I Human chr20 - 5599652 5599652 5599652 TACTAGGGAGGCTGAGGCAGGAGAATTGCTTGAACCTGGGAGGTGGAGGTTGCAGTGAGCCCAGA TACTAGGGAGGCTGAGGCAGGAGAATTGCTTGCACCTGGGAGGTGGAGGTTGCAGTGAGCCCAGA T G GPCPD1 Ensembl:ENSG00000125772 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1380009828 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_304782,RMVar_hsa_circ_208603,RMVar_hsa_circ_317545,RMVar_hsa_circ_52985,RMVar_hsa_circ_284624,RMVar_hsa_circ_112779,RMVar_hsa_circ_7694,RMVar_hsa_circ_208612,RMVar_hsa_circ_346212,RMVar_hsa_circ_208615,RMVar_hsa_circ_95579,RMVar_hsa_circ_100167,RMVar_hsa_circ_208616,RMVar_hsa_circ_348006 21732 RMVar_ID_21732 Human_SNP_ID_672453290 A-to-I Human chr20 - 5599825 5599825 5599825 ATTTTGGCTGGGCGCGGCGGCTCATGCCTGTAAACCCAGCACTTTGGGAGGCCAAGGCGGGCAGA ATTTTGGCTGGGCGCGGCGGCTCATGCCTGTACACCCAGCACTTTGGGAGGCCAAGGCGGGCAGA T G GPCPD1 Ensembl:ENSG00000125772 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1323017119 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_304782,RMVar_hsa_circ_208603,RMVar_hsa_circ_317545,RMVar_hsa_circ_52985,RMVar_hsa_circ_284624,RMVar_hsa_circ_112779,RMVar_hsa_circ_7694,RMVar_hsa_circ_208612,RMVar_hsa_circ_346212,RMVar_hsa_circ_208615,RMVar_hsa_circ_95579,RMVar_hsa_circ_100167,RMVar_hsa_circ_208616,RMVar_hsa_circ_348006 21733 RMVar_ID_21733 Human_SNP_ID_672453701 A-to-I Human chr20 - 5601507 5601507 5601507 AAAATTAGCCGGGCATGATGGTGCGTGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGACAGGAGA AAAATTAGCCGGGCATGATGGTGCGTGCCTGTGGTCCCAGCTACTCGGGAGGCTGAGACAGGAGA T C GPCPD1 Ensembl:ENSG00000125772 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1276027596 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_304782,RMVar_hsa_circ_208603,RMVar_hsa_circ_317545,RMVar_hsa_circ_52985,RMVar_hsa_circ_284624,RMVar_hsa_circ_112779,RMVar_hsa_circ_7694,RMVar_hsa_circ_208612,RMVar_hsa_circ_346212,RMVar_hsa_circ_208615,RMVar_hsa_circ_95579,RMVar_hsa_circ_100167,RMVar_hsa_circ_208616,RMVar_hsa_circ_348006 21734 RMVar_ID_21734 Human_SNP_ID_672453739 A-to-I Human chr20 - 5601628 5601628 5601628 ATGGTGGCTCATGCCTGTAATCCCAGCACTTTAGGAGGCCGAGGTGGGTGGATCATCTGAGGTCA ATGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGTGGATCATCTGAGGTCA T C GPCPD1 Ensembl:ENSG00000125772 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1357556695 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_304782,RMVar_hsa_circ_208603,RMVar_hsa_circ_317545,RMVar_hsa_circ_52985,RMVar_hsa_circ_284624,RMVar_hsa_circ_112779,RMVar_hsa_circ_7694,RMVar_hsa_circ_208612,RMVar_hsa_circ_346212,RMVar_hsa_circ_208615,RMVar_hsa_circ_95579,RMVar_hsa_circ_100167,RMVar_hsa_circ_208616,RMVar_hsa_circ_348006 21735 RMVar_ID_21735 Human_SNP_ID_672454067 A-to-I Human chr20 - 5602944 5602944 5602944 GAGTCTCACTCTGTTGCCTAGGCTGGAGTGCAATGACGCGATCTCGGCTCACTGCAACCTCTGCT GAGTCTCACTCTGTTGCCTAGGCTGGAGTGCAGTGACGCGATCTCGGCTCACTGCAACCTCTGCT T C GPCPD1 Ensembl:ENSG00000125772 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs962616386 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_304782,RMVar_hsa_circ_208603,RMVar_hsa_circ_317545,RMVar_hsa_circ_52985,RMVar_hsa_circ_284624,RMVar_hsa_circ_112779,RMVar_hsa_circ_7694,RMVar_hsa_circ_208612,RMVar_hsa_circ_346212,RMVar_hsa_circ_208615,RMVar_hsa_circ_95579,RMVar_hsa_circ_100167,RMVar_hsa_circ_208616,RMVar_hsa_circ_348006 21736 RMVar_ID_21736 Human_SNP_ID_672494757 A-to-I Human chr20 + 5751368 5751368 5751368 TCACTCTGTAGCCCAGGCTGGAGTATAGTGGCACGATCTTGGCTCACTGCAACCTCTGCTGCCCA TCACTCTGTAGCCCAGGCTGGAGTATAGTGGCGCGATCTTGGCTCACTGCAACCTCTGCTGCCCA A G SHLD1 Ensembl:ENSG00000171984 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1410799043 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97666,RMVar_hsa_circ_208619 21737 RMVar_ID_21737 Human_SNP_ID_672512029 A-to-I Human chr20 + 5820131 5820131 5820131 CACCATGCCTGGCTGATTTTTCTATTTTTAGTAGAGACAAGGTTTCACCATGTTGGTTGTCCAGG CACCATGCCTGGCTGATTTTTCTATTTTTAGTGGAGACAAGGTTTCACCATGTTGGTTGTCCAGG A G SHLD1 Ensembl:ENSG00000171984 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1221781685 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97666,RMVar_hsa_circ_76440,RMVar_hsa_circ_208619,RMVar_hsa_circ_208620 21738 RMVar_ID_21738 Human_SNP_ID_672512320 A-to-I Human chr20 + 5821453 5821453 5821453 GAGAATCGCTTGAACCAGGAGGCGGAGGTTGCAGTGAGCTGAGATCACACCACTGCACTCCAGCC GAGAATCGCTTGAACCAGGAGGCGGAGGTTGCGGTGAGCTGAGATCACACCACTGCACTCCAGCC A G SHLD1 Ensembl:ENSG00000171984 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1379265746 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97666,RMVar_hsa_circ_76440,RMVar_hsa_circ_208619,RMVar_hsa_circ_208620 21739 RMVar_ID_21739 Human_SNP_ID_672550852 A-to-I Human chr20 + 5970826 5970826 5970826 ACTGTTTTATATTCTTTCTCTTAATTTTTTTTAGAGACAGGGTCTTGCTGTGTTGCCCAGGCTGG ACTGTTTTATATTCTTTCTCTTAATTTTTTTTGGAGACAGGGTCTTGCTGTGTTGCCCAGGCTGG A G AL035461.4,MCM8 Ensembl:ENSG00000286235,Ensembl:ENSG00000125885 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs74853936 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_149367,Human_RBP_ID_7018216,Human_RBP_ID_17571365,Human_RBP_ID_25623718 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_285932,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 21740 RMVar_ID_21740 Human_SNP_ID_672550894 A-to-I Human chr20 + 5971052 5971052 5971052 CACAGGCTAGTTTTGAACTTTTGGGCTGAAGCAGTTCTTCCACCTTGGCCTCCCAGAGTGCTTGC CACAGGCTAGTTTTGAACTTTTGGGCTGAAGCGGTTCTTCCACCTTGGCCTCCCAGAGTGCTTGC A G AL035461.4,MCM8 Ensembl:ENSG00000286235,Ensembl:ENSG00000125885 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913850353 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14158275,Human_RBP_ID_17571366 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_285932,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 21741 RMVar_ID_21741 Human_SNP_ID_672551311 A-to-I Human chr20 + 5972694 5972694 5972694 CTCCCACCTCAGCCTGCCGAGTAGCTGGGACTACAGGCATGCGCCACCAGACCCAGCTACTTTTG CTCCCACCTCAGCCTGCCGAGTAGCTGGGACTGCAGGCATGCGCCACCAGACCCAGCTACTTTTG A G AL035461.4,MCM8 Ensembl:ENSG00000286235,Ensembl:ENSG00000125885 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1422023081 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2058939 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_126471,RMVar_hsa_circ_208627,RMVar_hsa_circ_349487,RMVar_hsa_circ_208628 21742 RMVar_ID_21742 Human_SNP_ID_672554675 A-to-I Human chr20 + 5985995 5985995 5985995 ATTGAGAAAGTACATTGGCTATGCTCGGCAGTATGTGTACCCAAGGCTATCCACAGAAGCTGCTC ATTGAGAAAGTACATTGGCTATGCTCGGCAGTGTGTGTACCCAAGGCTATCCACAGAAGCTGCTC A G AL035461.4,MCM8 Ensembl:ENSG00000286235,Ensembl:ENSG00000125885 Protein coding,Protein coding CDS,CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs376136067 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14158451,Human_RBP_ID_22817921 Human_Splice_Rec_2058876,Human_Splice_Rec_2058912,Human_Splice_Rec_2058948,Human_Splice_Rec_2058984,Human_Splice_Rec_2059020,Human_Splice_Rec_2059056 RMVar_hsa_circ_71789,RMVar_hsa_circ_353818,RMVar_hsa_circ_73413,RMVar_hsa_circ_278847,RMVar_hsa_circ_35848,RMVar_hsa_circ_74076,RMVar_hsa_circ_126471,RMVar_hsa_circ_208628,RMVar_hsa_circ_66040,RMVar_hsa_circ_58347,RMVar_hsa_circ_338742,RMVar_hsa_circ_311061 21743 RMVar_ID_21743 Human_SNP_ID_672554676 A-to-I Human chr20 + 5985995 5985995 5985995 ATTGAGAAAGTACATTGGCTATGCTCGGCAGTATGTGTACCCAAGGCTATCCACAGAAGCTGCTC ATTGAGAAAGTACATTGGCTATGCTCGGCAGTTTGTGTACCCAAGGCTATCCACAGAAGCTGCTC A T AL035461.4,MCM8 Ensembl:ENSG00000286235,Ensembl:ENSG00000125885 Protein coding,Protein coding CDS,CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs376136067 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14158451,Human_RBP_ID_22817921 Human_Splice_Rec_2058876,Human_Splice_Rec_2058912,Human_Splice_Rec_2058948,Human_Splice_Rec_2058984,Human_Splice_Rec_2059020,Human_Splice_Rec_2059056 RMVar_hsa_circ_71789,RMVar_hsa_circ_353818,RMVar_hsa_circ_73413,RMVar_hsa_circ_278847,RMVar_hsa_circ_35848,RMVar_hsa_circ_74076,RMVar_hsa_circ_126471,RMVar_hsa_circ_208628,RMVar_hsa_circ_66040,RMVar_hsa_circ_58347,RMVar_hsa_circ_338742,RMVar_hsa_circ_311061 21744 RMVar_ID_21744 Human_SNP_ID_672556789 A-to-I Human chr20 + 5994631 5994631 5994631 ATTTAAGAAGTGATAAAGTCTCCAGATGCAGTAGCTCACACTGTAATCACAGTGACTCAGGAGGC ATTTAAGAAGTGATAAAGTCTCCAGATGCAGTGGCTCACACTGTAATCACAGTGACTCAGGAGGC A G AL035461.4,MCM8 Ensembl:ENSG00000286235,Ensembl:ENSG00000125885 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1051583 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_206545,Human_RBP_ID_24533852 21745 RMVar_ID_21745 Human_SNP_ID_672556840 A-to-I Human chr20 + 5994786 5994786 5994786 TTAAACTTAGCTGGGTATGGTGGCACATGCCTATAGTCTCAGCTACTTGTGAGGCTGAGGCAGGA TTAAACTTAGCTGGGTATGGTGGCACATGCCTGTAGTCTCAGCTACTTGTGAGGCTGAGGCAGGA A G AL035461.4,MCM8 Ensembl:ENSG00000286235,Ensembl:ENSG00000125885 Protein coding,Protein coding intron,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1131807 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4655204,Human_RBP_ID_18167931 21746 RMVar_ID_21746 Human_SNP_ID_672557096 A-to-I Human chr20 + 5996003 5995998 5996003 GAGGAAGGAAAAATCAGGAATCAAAAGGGGCCAGGTGCAGTGGCTCACATCTATAATCCCAGAGC GAGGAAGGAAAAATCAGGAATCAAAAGG_____GGTGCAGTGGCTCACATCTATAATCCCAGAGC GGGCCA G AL035461.4,MCM8 Ensembl:ENSG00000286235,Ensembl:ENSG00000125885 Protein coding,Protein coding intron,3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1322370776 Functional Loss DEL dbSNP153 29..33 33 - - - 21747 RMVar_ID_21747 Human_SNP_ID_672557098 A-to-I Human chr20 + 5996003 5996003 5996003 GAGGAAGGAAAAATCAGGAATCAAAAGGGGCCAGGTGCAGTGGCTCACATCTATAATCCCAGAGC GAGGAAGGAAAAATCAGGAATCAAAAGGGGCCTGGTGCAGTGGCTCACATCTATAATCCCAGAGC A T AL035461.4,MCM8 Ensembl:ENSG00000286235,Ensembl:ENSG00000125885 Protein coding,Protein coding intron,3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1017312888 Functional Loss SNV dbSNP153 33..33 33 - - - 21748 RMVar_ID_21748 Human_SNP_ID_672557128 A-to-I Human chr20 + 5996152 5996152 5996152 AATAGATTAGCTGGGCACGGTGGTGCATGCCTATTGTCCTACCTACTGTGGAGGCTGAAGTAGGA AATAGATTAGCTGGGCACGGTGGTGCATGCCTGTTGTCCTACCTACTGTGGAGGCTGAAGTAGGA A G AL035461.4,MCM8 Ensembl:ENSG00000286235,Ensembl:ENSG00000125885 Protein coding,Protein coding intron,3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs915974994 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5445832 21749 RMVar_ID_21749 Human_SNP_ID_672557200 A-to-I Human chr20 + 5996422 5996422 5996422 CCTGTAGTCCCAGCCACTAAGGAGGCTGAGGCAGGAGAATCACTTGAACCCGGGAGGCAGAGGTT CCTGTAGTCCCAGCCACTAAGGAGGCTGAGGCGGGAGAATCACTTGAACCCGGGAGGCAGAGGTT A G AL035461.4,MCM8 Ensembl:ENSG00000286235,Ensembl:ENSG00000125885 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs960297577 Functional Loss SNV dbSNP153 33..33 33 - - - 21750 RMVar_ID_21750 Human_SNP_ID_672557513 A-to-I Human chr20 + 5997544 5997544 5997544 GCCATGTTGTCCAGTATGGACTTGAACTACTCAGCTCAAGCAGTCCTCCCACCTCAGCCTCCTGA GCCATGTTGTCCAGTATGGACTTGAACTACTCGGCTCAAGCAGTCCTCCCACCTCAGCCTCCTGA A G AL035461.4,MCM8 Ensembl:ENSG00000286235,Ensembl:ENSG00000125885 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs957733344 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14158646 21751 RMVar_ID_21751 Human_SNP_ID_672557555 A-to-I Human chr20 + 5997716 5997716 5997716 GCCGTGATCTCCTGGGCTCAAGCAATCCTCCTACCTCAGCCTCCTGAGTAGCTGGAACTACAGGA GCCGTGATCTCCTGGGCTCAAGCAATCCTCCTGCCTCAGCCTCCTGAGTAGCTGGAACTACAGGA A G AL035461.4,MCM8 Ensembl:ENSG00000286235,Ensembl:ENSG00000125885 Protein coding,Protein coding intron,3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1212775762 Functional Loss SNV dbSNP153 33..33 33 - - - 21752 RMVar_ID_21752 Human_SNP_ID_672557816 A-to-I Human chr20 + 5998872 5998872 5998872 ATACCAGGCTTGCTCTAGAGCGTGGGCTTGGGAATGGAAAGGCAGAGTGCACCTATTGAATTCCA ATACCAGGCTTGCTCTAGAGCGTGGGCTTGGGGATGGAAAGGCAGAGTGCACCTATTGAATTCCA A G AL035461.4,MCM8 Ensembl:ENSG00000286235,Ensembl:ENSG00000125885 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs542092694 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8856644,Human_RBP_ID_14158699,Human_RBP_ID_17396350 21753 RMVar_ID_21753 Human_SNP_ID_672557961 A-to-I Human chr20 + 5999245 5999244 5999246 ACTAGTGTGTATATATATATACACTAGAGTATACACACTCTAGAGTATACACTCTATAAAGTATA ACTAGTGTGTATATATATATACACTAGAGTAT__ACACTCTAGAGTATACACTCTATAAAGTATA TAC T AL035461.4 Ensembl:ENSG00000286235 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1303730646 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_8537473 21754 RMVar_ID_21754 Human_SNP_ID_672558070 A-to-I Human chr20 + 5999426 5999425 5999427 ACTATATATAGTCTATATACTCTAGAGAGTACAGTATATATATATAGTGTATATATACTCTATGG ACTATATATAGTCTATATACTCTAGAGAGTAC__TATATATATATAGTGTATATATACTCTATGG CAG C AL035461.4 Ensembl:ENSG00000286235 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1168307771 Functional Loss DEL dbSNP153 33..34 33 - - - 21755 RMVar_ID_21755 Human_SNP_ID_672558207 A-to-I Human chr20 + 6000050 6000050 6000050 GGAGTTTCGCTCTGTCATCCATGCTGGAGTGCAATGGTGAGATCTCGACTCACTGCAACTTCCGC GGAGTTTCGCTCTGTCATCCATGCTGGAGTGCGATGGTGAGATCTCGACTCACTGCAACTTCCGC A G AL035461.4 Ensembl:ENSG00000286235 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs571558141 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14158727 21756 RMVar_ID_21756 Human_SNP_ID_672558238 A-to-I Human chr20 + 6000157 6000157 6000157 GAGATTACAGGTGCGTGCCATCATGCCCGGCTAATTTTTGTATTTTTAGTAGAGACGAGGTTTCA GAGATTACAGGTGCGTGCCATCATGCCCGGCTCATTTTTGTATTTTTAGTAGAGACGAGGTTTCA A C AL035461.4 Ensembl:ENSG00000286235 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1486842559 Functional Loss SNV dbSNP153 33..33 33 - - - 21757 RMVar_ID_21757 Human_SNP_ID_672567256 A-to-I Human chr20 + 6037717 6037717 6037717 TATAAAAGAGATTAAAAATGCGGTAACTTTTTAAGATAATAATCATACAGAAGGTATGAAGTTCA TATAAAAGAGATTAAAAATGCGGTAACTTTTTCAGATAATAATCATACAGAAGGTATGAAGTTCA A C AL035461.4,CRLS1 Ensembl:ENSG00000286235,Ensembl:ENSG00000088766 Protein coding,Protein coding 3'UTR,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879468804 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2692287,Human_RBP_ID_17975277,Human_RBP_ID_27703841 Human_miRNA_ID_127860 21758 RMVar_ID_21758 Human_SNP_ID_672567257 A-to-I Human chr20 + 6037717 6037717 6037717 TATAAAAGAGATTAAAAATGCGGTAACTTTTTAAGATAATAATCATACAGAAGGTATGAAGTTCA TATAAAAGAGATTAAAAATGCGGTAACTTTTTTAGATAATAATCATACAGAAGGTATGAAGTTCA A T AL035461.4,CRLS1 Ensembl:ENSG00000286235,Ensembl:ENSG00000088766 Protein coding,Protein coding 3'UTR,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879468804 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2692287,Human_RBP_ID_17975277,Human_RBP_ID_27703841 Human_miRNA_ID_127860 21759 RMVar_ID_21759 Human_SNP_ID_673098519 A-to-I Human chr20 + 8171116 8171116 8171116 TTACCTCTGATTTTAGATAGAGTTTATGACACATGCTCTGTAAATATCAAGTGAAGTTATTTTAG TTACCTCTGATTTTAGATAGAGTTTATGACACGTGCTCTGTAAATATCAAGTGAAGTTATTTTAG A G PLCB1 Ensembl:ENSG00000182621 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1300219584 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571369 RMVar_hsa_circ_360013 21760 RMVar_ID_21760 Human_SNP_ID_673119137 A-to-I Human chr20 + 8260273 8260273 8260273 CAGCATTTTTTTTTTTTTTTTCTGTTAGAGACAAGGTCTTTCCATAGTGCCCAGACTGGTCTCAA CAGCATTTTTTTTTTTTTTTTCTGTTAGAGACGAGGTCTTTCCATAGTGCCCAGACTGGTCTCAA A G PLCB1 Ensembl:ENSG00000182621 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs994342259 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571375 RMVar_hsa_circ_360013 21761 RMVar_ID_21761 Human_SNP_ID_673119921 A-to-I Human chr20 + 8263582 8263581 8263582 CTGATATTGTGTGAACATCAGGGACTGAACTTATGCAAACCTAGATGGTAGAGACTACTACATAC CTGATATTGTGTGAACATCAGGGACTGAACTT_TGCAAACCTAGATGGTAGAGACTACTACATAC TA T PLCB1 Ensembl:ENSG00000182621 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1368055081 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_360013 21762 RMVar_ID_21762 Human_SNP_ID_673119922 A-to-I Human chr20 + 8263582 8263582 8263582 CTGATATTGTGTGAACATCAGGGACTGAACTTATGCAAACCTAGATGGTAGAGACTACTACATAC CTGATATTGTGTGAACATCAGGGACTGAACTTCTGCAAACCTAGATGGTAGAGACTACTACATAC A C PLCB1 Ensembl:ENSG00000182621 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1299163802 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_360013 21763 RMVar_ID_21763 Human_SNP_ID_673153139 A-to-I Human chr20 + 8407680 8407680 8407680 ACAATATGTGGGAATTCTGAGAGATACAAATCAGGTTGAGATTTGGGTGGGGACACAGCCAAACC ACAATATGTGGGAATTCTGAGAGATACAAATCGGGTTGAGATTTGGGTGGGGACACAGCCAAACC A G PLCB1 Ensembl:ENSG00000182621 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs537689040 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_208648,RMVar_hsa_circ_208649 21764 RMVar_ID_21764 Human_SNP_ID_673180917 A-to-I Human chr20 + 8527413 8527413 8527413 TACAAATGAAAATAAATAAACAGCATGGATTCAATAACTATACTGCGAGTCAAGACTACTCTTAT TACAAATGAAAATAAATAAACAGCATGGATTCCATAACTATACTGCGAGTCAAGACTACTCTTAT A C PLCB1 Ensembl:ENSG00000182621 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1263597834 Functional Loss SNV dbSNP153 33..33 33 - - - 21765 RMVar_ID_21765 Human_SNP_ID_673267032 A-to-I Human chr20 + 8884768 8884766 8884768 TAAAATGTACATATTTTGGTTCTTCTATCTCAAATTATTTAAAATGCATAATTCACATTTTTGTA TAAAATGTACATATTTTGGTTCTTCTATCTC__ATTATTTAAAATGCATAATTCACATTTTTGTA CAA C PLCB1 Ensembl:ENSG00000182621 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1456349884 Functional Loss DEL dbSNP153 32..33 33 - - - 21766 RMVar_ID_21766 Human_SNP_ID_673316660 A-to-I Human chr20 + 9098836 9098836 9098836 GAATTAATTGCCACATACTCCAGGTCTTTTACAATACTCCACAGCCTCCTGGGCTCTGTCACCCA GAATTAATTGCCACATACTCCAGGTCTTTTACGATACTCCACAGCCTCCTGGGCTCTGTCACCCA A G PLCB4 Ensembl:ENSG00000101333 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1195858215 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_329451,RMVar_hsa_circ_340982 21767 RMVar_ID_21767 Human_SNP_ID_673316699 A-to-I Human chr20 + 9098951 9098951 9098951 ATATATATATATGTATGTATATATACGTATATATATATGACTATTTTAAAACTCTGTATCATTCC ATATATATATATGTATGTATATATACGTATATGTATATGACTATTTTAAAACTCTGTATCATTCC A G PLCB4 Ensembl:ENSG00000101333 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1301530475 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_329451,RMVar_hsa_circ_340982 21768 RMVar_ID_21768 Human_SNP_ID_673387257 A-to-I Human chr20 + 9413779 9413779 9413779 CTCACTCTCTCCACCGTTATTTATTTTTTCTTAAGACAGGGTTTCGCTCTGTCACCCAGGCTCAA CTCACTCTCTCCACCGTTATTTATTTTTTCTTGAGACAGGGTTTCGCTCTGTCACCCAGGCTCAA A G PLCB4 Ensembl:ENSG00000101333 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1243015755 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76629,RMVar_hsa_circ_11565,RMVar_hsa_circ_67635,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_30490,RMVar_hsa_circ_1469,RMVar_hsa_circ_27258,RMVar_hsa_circ_18034,RMVar_hsa_circ_35321,RMVar_hsa_circ_317730,RMVar_hsa_circ_208679,RMVar_hsa_circ_208680 21769 RMVar_ID_21769 Human_SNP_ID_673387273 A-to-I Human chr20 + 9413824 9413824 9413824 GCTCTGTCACCCAGGCTCAAGTGCAGTGGTGCAAACGTGGCTCATTGAGGCCTTGACATCCTGGG GCTCTGTCACCCAGGCTCAAGTGCAGTGGTGCGAACGTGGCTCATTGAGGCCTTGACATCCTGGG A G PLCB4 Ensembl:ENSG00000101333 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749789069 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76629,RMVar_hsa_circ_11565,RMVar_hsa_circ_67635,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_30490,RMVar_hsa_circ_1469,RMVar_hsa_circ_27258,RMVar_hsa_circ_18034,RMVar_hsa_circ_35321,RMVar_hsa_circ_317730,RMVar_hsa_circ_208679,RMVar_hsa_circ_208680 21770 RMVar_ID_21770 Human_SNP_ID_673390161 A-to-I Human chr20 + 9426511 9426511 9426511 GGCGATTCTCCTGTCTCAGCCTCCCGATAGCTAGAACTACAGGCGTGCACCACTATGCCCAGCTA GGCGATTCTCCTGTCTCAGCCTCCCGATAGCTGGAACTACAGGCGTGCACCACTATGCCCAGCTA A G PLCB4 Ensembl:ENSG00000101333 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1242472404 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_909,RMVar_hsa_circ_76629,RMVar_hsa_circ_67635,RMVar_hsa_circ_208672,RMVar_hsa_circ_30490,RMVar_hsa_circ_1469,RMVar_hsa_circ_35321,RMVar_hsa_circ_317730,RMVar_hsa_circ_208679,RMVar_hsa_circ_208680,RMVar_hsa_circ_314542,RMVar_hsa_circ_20225,RMVar_hsa_circ_6019,RMVar_hsa_circ_208682,RMVar_hsa_circ_3233 21771 RMVar_ID_21771 Human_SNP_ID_673544149 A-to-I Human chr20 + 10056330 10056330 10056330 AGATAGATAGCCCTAGCCCTAGATAGATAGCTATTAGGTTGGTGCAAAAGTAATTGTGGTTTTTG AGATAGATAGCCCTAGCCCTAGATAGATAGCTGTTAGGTTGGTGCAAAAGTAATTGTGGTTTTTG A G ANKEF1 Ensembl:ENSG00000132623 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991970704 Functional Loss SNV dbSNP153 33..33 33 - - - 21772 RMVar_ID_21772 Human_SNP_ID_673592306 A-to-I Human chr20 + 10249760 10249760 10249760 TAGATTTGGAGCCCAGGAATCTGTGTTTTAATAAGTTCTCCAGGTGATTTTTAGAAGCCCTAGTC TAGATTTGGAGCCCAGGAATCTGTGTTTTAATGAGTTCTCCAGGTGATTTTTAGAAGCCCTAGTC A G SNAP25 Ensembl:ENSG00000132639 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs558126498 Functional Loss SNV dbSNP153 33..33 33 - - - 21773 RMVar_ID_21773 Human_SNP_ID_673633786 A-to-I Human chr20 - 10428717 10428716 10428717 CTCCTGTTTCAGCCTCCCAGGTAACTGGGATTACAGGTGCACCCACCACATCCAGCTAATTTTTC CTCCTGTTTCAGCCTCCCAGGTAACTGGGATT_CAGGTGCACCCACCACATCCAGCTAATTTTTC GT G AL034430.1,MKKS Ensembl:ENSG00000285508,Ensembl:ENSG00000125863 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1331806445 Functional Loss DEL dbSNP153 33..33 33 - - - Human_Splice_Rec_2061236 21774 RMVar_ID_21774 Human_SNP_ID_673650769 A-to-I Human chr20 + 10500198 10500198 10500198 ACTCTGTTGCCCAGGCTGGAGTGCAATGGTGCAATCTCAGCTCACTGCAACCTCTGAATTGTTCA ACTCTGTTGCCCAGGCTGGAGTGCAATGGTGCGATCTCAGCTCACTGCAACCTCTGAATTGTTCA A G SLX4IP Ensembl:ENSG00000149346 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1437610402 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_347164 21775 RMVar_ID_21775 Human_SNP_ID_673650886 A-to-I Human chr20 + 10500700 10500700 10500700 CTTGAGCCCAGGAGGTCGAGGCTGCATGAGCTATGACTGCACCTCTGCACTCTAGCCTGGATGAC CTTGAGCCCAGGAGGTCGAGGCTGCATGAGCTGTGACTGCACCTCTGCACTCTAGCCTGGATGAC A G SLX4IP Ensembl:ENSG00000149346 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256208289 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_347164 21776 RMVar_ID_21776 Human_SNP_ID_673998457 A-to-I Human chr20 + 11895320 11895320 11895320 TTAACATTACAATTCTATGCCCTTGTCCTTTCAGATAAAGATTATTGTATTTAATACATGCACAG TTAACATTACAATTCTATGCCCTTGTCCTTTCGGATAAAGATTATTGTATTTAATACATGCACAG A G BTBD3 Ensembl:ENSG00000132640 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1226947978 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109284,RMVar_hsa_circ_208733 21777 RMVar_ID_21777 Human_SNP_ID_673998459 A-to-I Human chr20 + 11895322 11895322 11895322 AACATTACAATTCTATGCCCTTGTCCTTTCAGATAAAGATTATTGTATTTAATACATGCACAGTT AACATTACAATTCTATGCCCTTGTCCTTTCAGGTAAAGATTATTGTATTTAATACATGCACAGTT A G BTBD3 Ensembl:ENSG00000132640 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs951794408 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109284,RMVar_hsa_circ_208733 21778 RMVar_ID_21778 Human_SNP_ID_673999149 A-to-I Human chr20 + 11897971 11897971 11897971 CTTGAGGTCAGCAGTTGAAGACCAGCCCGGCCAACATGGTGAAACCTTATGTCTACTAAAAATAC CTTGAGGTCAGCAGTTGAAGACCAGCCCGGCCGACATGGTGAAACCTTATGTCTACTAAAAATAC A G BTBD3 Ensembl:ENSG00000132640 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1345586844 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109284,RMVar_hsa_circ_208733 21779 RMVar_ID_21779 Human_SNP_ID_674477913 A-to-I Human chr20 + 13803966 13803966 13803966 TGCCACCACGCCCCATTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGTC TGCCACCACGCCCCATTAATTTTTGTATTTTTGGTAGAGATGGGGTTTCACCATGTTGGCCAGTC A G NDUFAF5 Ensembl:ENSG00000101247 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041690514 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36319,RMVar_hsa_circ_365137,RMVar_hsa_circ_53524,RMVar_hsa_circ_46336,RMVar_hsa_circ_364767 21780 RMVar_ID_21780 Human_SNP_ID_674478600 A-to-I Human chr20 + 13806930 13806930 13806930 TCTTCCTGACTTCTCCCTCTGTTGCCCAGGCTAGAGTGCAGTGGCGAGATCTCCGCTTACTGCAA TCTTCCTGACTTCTCCCTCTGTTGCCCAGGCTGGAGTGCAGTGGCGAGATCTCCGCTTACTGCAA A G NDUFAF5 Ensembl:ENSG00000101247 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935417365 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36319,RMVar_hsa_circ_365137,RMVar_hsa_circ_53524,RMVar_hsa_circ_46336,RMVar_hsa_circ_364767 21781 RMVar_ID_21781 Human_SNP_ID_674478658 A-to-I Human chr20 + 13807111 13807111 13807111 CTCTTTCACCCAGGTTGGAGTGCCGTGGCGTGATCTCGGCTCACTGCAACCTCTGCCTCCCGGGT CTCTTTCACCCAGGTTGGAGTGCCGTGGCGTGTTCTCGGCTCACTGCAACCTCTGCCTCCCGGGT A T NDUFAF5 Ensembl:ENSG00000101247 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1437931137 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36319,RMVar_hsa_circ_365137,RMVar_hsa_circ_53524,RMVar_hsa_circ_46336,RMVar_hsa_circ_364767 21782 RMVar_ID_21782 Human_SNP_ID_674505999 A-to-I Human chr20 - 13919064 13919064 13919064 CAGATGAAGGAGACCAGCTATTTAAGATGGGCATCAAGGTTCTCCAGCAGTCTAAAAGCCAAAAA CAGATGAAGGAGACCAGCTATTTAAGATGGGCGTCAAGGTTCTCCAGCAGTCTAAAAGCCAAAAA T C SEL1L2 Ensembl:ENSG00000101251 Protein coding CDS GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs543966458 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2062450,Human_Splice_Rec_2062451,Human_Splice_Rec_2062488,Human_Splice_Rec_2062489,Human_Splice_Rec_2062528,Human_Splice_Rec_2062529,Human_Splice_Rec_2062562,Human_Splice_Rec_2062563,Human_Splice_Rec_2062598,Human_Splice_Rec_2062599,Human_Splice_Rec_2062631,Human_Splice_Rec_2062640,Human_Splice_Rec_2062641 21783 RMVar_ID_21783 Human_SNP_ID_674506000 A-to-I Human chr20 - 13919064 13919064 13919064 CAGATGAAGGAGACCAGCTATTTAAGATGGGCATCAAGGTTCTCCAGCAGTCTAAAAGCCAAAAA CAGATGAAGGAGACCAGCTATTTAAGATGGGCCTCAAGGTTCTCCAGCAGTCTAAAAGCCAAAAA T G SEL1L2 Ensembl:ENSG00000101251 Protein coding CDS GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs543966458 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2062450,Human_Splice_Rec_2062451,Human_Splice_Rec_2062488,Human_Splice_Rec_2062489,Human_Splice_Rec_2062528,Human_Splice_Rec_2062529,Human_Splice_Rec_2062562,Human_Splice_Rec_2062563,Human_Splice_Rec_2062598,Human_Splice_Rec_2062599,Human_Splice_Rec_2062631,Human_Splice_Rec_2062640,Human_Splice_Rec_2062641 21784 RMVar_ID_21784 Human_SNP_ID_675403225 A-to-I Human chr20 + 17575106 17575106 17575106 GTCTCAAACAATCTTCCCGCTTTGGCCTCCCAAAGTGTTGGGATTACAGGCATGAGCCATTGTGC GTCTCAAACAATCTTCCCGCTTTGGCCTCCCAGAGTGTTGGGATTACAGGCATGAGCCATTGTGC A G DSTN Ensembl:ENSG00000125868 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1337022527 Functional Loss SNV dbSNP153 33..33 33 - - - 21785 RMVar_ID_21785 Human_SNP_ID_675408580 A-to-I Human chr20 + 17598095 17598095 17598095 TATACTACATCTTAAAAATCTATTCATCACTAAATGGACTTTAGGATTGTTTTCACTTTTGGTCT TATACTACATCTTAAAAATCTATTCATCACTAGATGGACTTTAGGATTGTTTTCACTTTTGGTCT A G DSTN Ensembl:ENSG00000125868 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs117016945 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22186,RMVar_hsa_circ_208856,RMVar_hsa_circ_110376 21786 RMVar_ID_21786 Human_SNP_ID_675411061 A-to-I Human chr20 + 17608568 17608568 17608568 GGGAGGATCACTTGAGCCCAGGAGGTGAGCTGAGATCGTGCCACTGTACTCCAGCCTGGATGACA GGGAGGATCACTTGAGCCCAGGAGGTGAGCTGCGATCGTGCCACTGTACTCCAGCCTGGATGACA A C DSTN Ensembl:ENSG00000125868 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1200011778 Functional Loss SNV dbSNP153 33..33 33 - - - 21787 RMVar_ID_21787 Human_SNP_ID_675411279 A-to-I Human chr20 + 17609307 17609307 17609307 CTCACTGCATCCTTGAACTCTTGGGCTCCAGCAAGCCTCCTGCCTTGGCCTCCTAAAGTGCTGTG CTCACTGCATCCTTGAACTCTTGGGCTCCAGCTAGCCTCCTGCCTTGGCCTCCTAAAGTGCTGTG A T DSTN Ensembl:ENSG00000125868 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1379487681 Functional Loss SNV dbSNP153 33..33 33 - - - 21788 RMVar_ID_21788 Human_SNP_ID_675431651 A-to-I Human chr20 - 17677589 17677589 17677589 GTGATCTGCCCTCCTCGGCCTCCCAAAGTGCTAGGATTATAGGCATGAGCCACCGTGCCCGGCCT GTGATCTGCCCTCCTCGGCCTCCCAAAGTGCTGGGATTATAGGCATGAGCCACCGTGCCCGGCCT T C RRBP1 Ensembl:ENSG00000125844 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1438339529 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91274,RMVar_hsa_circ_208859,RMVar_hsa_circ_57569,RMVar_hsa_circ_356409 21789 RMVar_ID_21789 Human_SNP_ID_675502738 A-to-I Human chr20 - 17957271 17957271 17957271 GCCACCACGCTTAGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTAGCCAGGA GCCACCACGCTTAGCTAATTTTTTGTATTTTTCGTAGAGACGGGGTTTCACCATGTTAGCCAGGA T G SNX5,OVOL2 Ensembl:ENSG00000089006,Ensembl:ENSG00000125850 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1392092412 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4170,RMVar_hsa_circ_318512,RMVar_hsa_circ_277337 21790 RMVar_ID_21790 Human_SNP_ID_675503682 A-to-I Human chr20 - 17960532 17960532 17960532 TGGAGTGCAGTCGCGTGATGTCGGCTCACTGCAACCTCTGCCTCCTGGGTTCAAGCGATTCTCCT TGGAGTGCAGTCGCGTGATGTCGGCTCACTGCCACCTCTGCCTCCTGGGTTCAAGCGATTCTCCT T G SNX5,OVOL2 Ensembl:ENSG00000089006,Ensembl:ENSG00000125850 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1364555452 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14042932 Human_miRNA_ID_2274105,Human_miRNA_ID_2476811,Human_miRNA_ID_2962592,Human_miRNA_ID_2995380 RMVar_hsa_circ_4170,RMVar_hsa_circ_318512,RMVar_hsa_circ_277337 21791 RMVar_ID_21791 Human_SNP_ID_675503700 A-to-I Human chr20 - 17960594 17960594 17960594 TTGTGTGTGTTTTTTTGTTTGTTTGTTTTTTTAAGACGGAGTTTCGCTCTCATCGCCCAGGCTGG TTGTGTGTGTTTTTTTGTTTGTTTGTTTTTTTTAGACGGAGTTTCGCTCTCATCGCCCAGGCTGG T A SNX5,OVOL2 Ensembl:ENSG00000089006,Ensembl:ENSG00000125850 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1568596270 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2678221,Human_RBP_ID_3643750,Human_RBP_ID_6981751,Human_RBP_ID_14042932 RMVar_hsa_circ_4170,RMVar_hsa_circ_318512,RMVar_hsa_circ_277337 21792 RMVar_ID_21792 Human_SNP_ID_675504301 A-to-I Human chr20 - 17962329 17962329 17962329 GGGGTGGTGGGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGTATCTGGGAGAATTG GGGGTGGTGGGCGCCTGTAATCCCAGCTACTCCGGAGGCTGAGGCAGGAGTATCTGGGAGAATTG T G SNX5,OVOL2 Ensembl:ENSG00000089006,Ensembl:ENSG00000125850 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1473860839 Functional Loss SNV dbSNP153 33..33 33 - - - 21793 RMVar_ID_21793 Human_SNP_ID_675504303 A-to-I Human chr20 - 17962333 17962333 17962333 GGGTGGGGTGGTGGGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGTATCTGGGAGA GGGTGGGGTGGTGGGCGCCTGTAATCCCAGCTTCTCAGGAGGCTGAGGCAGGAGTATCTGGGAGA T A SNX5,OVOL2 Ensembl:ENSG00000089006,Ensembl:ENSG00000125850 Protein coding,Protein coding intron,intron GSE47997;GSE100210;GSE99789 K562 cells&HepG2 cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 23474544,29129909,29796672 RNA-Seq:(High) rs879004931 Functional Loss SNV dbSNP153 33..33 33 - - - 21794 RMVar_ID_21794 Human_SNP_ID_675504307 A-to-I Human chr20 - 17962343 17962343 17962343 AAAATTAGCTGGGTGGGGTGGTGGGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGT AAAATTAGCTGGGTGGGGTGGTGGGCGCCTGTGATCCCAGCTACTCAGGAGGCTGAGGCAGGAGT T C SNX5,OVOL2 Ensembl:ENSG00000089006,Ensembl:ENSG00000125850 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs78790618 Functional Loss SNV dbSNP153 33..33 33 - - - 21795 RMVar_ID_21795 Human_SNP_ID_675504335 A-to-I Human chr20 - 17962408 17962407 17962408 ACGAGGTCAGGAGTTAGAGACCAGCCTGACCAACATGGTGAAACCCTGTCTCTACTAAAAATACA ACGAGGTCAGGAGTTAGAGACCAGCCTGACCA_CATGGTGAAACCCTGTCTCTACTAAAAATACA GT G SNX5,OVOL2 Ensembl:ENSG00000089006,Ensembl:ENSG00000125850 Protein coding,Protein coding intron,intron GSE99789;GSE126723:GSM3611833,GSM3611834,GSM3611835 esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BERP35T4 cell line - 29796672,31158229 RNA-Seq:(High) rs11475300 Functional Loss DEL dbSNP153 33..33 33 - - - 21796 RMVar_ID_21796 Human_SNP_ID_675504336 A-to-I Human chr20 - 17962412 17962412 17962412 GATCACGAGGTCAGGAGTTAGAGACCAGCCTGACCAACATGGTGAAACCCTGTCTCTACTAAAAA GATCACGAGGTCAGGAGTTAGAGACCAGCCTGTCCAACATGGTGAAACCCTGTCTCTACTAAAAA T A SNX5,OVOL2 Ensembl:ENSG00000089006,Ensembl:ENSG00000125850 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1006786522 Functional Loss SNV dbSNP153 33..33 33 - - - 21797 RMVar_ID_21797 Human_SNP_ID_675504337 A-to-I Human chr20 - 17962412 17962412 17962412 GATCACGAGGTCAGGAGTTAGAGACCAGCCTGACCAACATGGTGAAACCCTGTCTCTACTAAAAA GATCACGAGGTCAGGAGTTAGAGACCAGCCTGGCCAACATGGTGAAACCCTGTCTCTACTAAAAA T C SNX5,OVOL2 Ensembl:ENSG00000089006,Ensembl:ENSG00000125850 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1006786522 Functional Loss SNV dbSNP153 33..33 33 - - - 21798 RMVar_ID_21798 Human_SNP_ID_675504349 A-to-I Human chr20 - 17962475 17962475 17962475 AGTTGGGCTGGGCGCGGTGGCTCACGCCTATAATCCCAGGACTTTGGGAGGCTGAGGCGGGCAGA AGTTGGGCTGGGCGCGGTGGCTCACGCCTATATTCCCAGGACTTTGGGAGGCTGAGGCGGGCAGA T A SNX5,OVOL2 Ensembl:ENSG00000089006,Ensembl:ENSG00000125850 Protein coding,Protein coding intron,intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs965269671 Functional Loss SNV dbSNP153 33..33 33 - - - 21799 RMVar_ID_21799 Human_SNP_ID_675504350 A-to-I Human chr20 - 17962476 17962476 17962476 GAGTTGGGCTGGGCGCGGTGGCTCACGCCTATAATCCCAGGACTTTGGGAGGCTGAGGCGGGCAG GAGTTGGGCTGGGCGCGGTGGCTCACGCCTATGATCCCAGGACTTTGGGAGGCTGAGGCGGGCAG T C SNX5,OVOL2 Ensembl:ENSG00000089006,Ensembl:ENSG00000125850 Protein coding,Protein coding intron,intron GSE47997;GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 23474544,24183664,29129909,31158229,31158229 RNA-Seq:(High) rs904236090 Functional Loss SNV dbSNP153 33..33 33 - - - 21800 RMVar_ID_21800 Human_SNP_ID_675504351 A-to-I Human chr20 - 17962478 17962478 17962478 CAGAGTTGGGCTGGGCGCGGTGGCTCACGCCTATAATCCCAGGACTTTGGGAGGCTGAGGCGGGC CAGAGTTGGGCTGGGCGCGGTGGCTCACGCCTGTAATCCCAGGACTTTGGGAGGCTGAGGCGGGC T C SNX5,OVOL2 Ensembl:ENSG00000089006,Ensembl:ENSG00000125850 Protein coding,Protein coding intron,intron GSE47997;GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,24183664,29129909,31158229,31158229 RNA-Seq:(High) rs1222850915 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7024046,Human_RBP_ID_14175293,Human_RBP_ID_25594400 21801 RMVar_ID_21801 Human_SNP_ID_675507457 A-to-I Human chr20 + 17971848 17971848 17971848 GACTTGACCGCCGGGACCCAAGTGATTCTCCCATCTCAGCCTGCTGAGTAGCTGGGACCACAGGC GACTTGACCGCCGGGACCCAAGTGATTCTCCCGTCTCAGCCTGCTGAGTAGCTGGGACCACAGGC A G MGME1 Ensembl:ENSG00000125871 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs8119510 Functional Loss SNV dbSNP153 33..33 33 - - - 21802 RMVar_ID_21802 Human_SNP_ID_675507483 A-to-I Human chr20 + 17971946 17971946 17971946 TTTGTAGCGACAAGGGTCTCCCTATGTTGCCCAGGCTAGTCTCCAACTCCTGTCTTCAAGTGGTG TTTGTAGCGACAAGGGTCTCCCTATGTTGCCCGGGCTAGTCTCCAACTCCTGTCTTCAAGTGGTG A G MGME1 Ensembl:ENSG00000125871 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs558401531 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244853,Human_RBP_ID_14043592 21803 RMVar_ID_21803 Human_SNP_ID_675507493 A-to-I Human chr20 + 17972002 17972002 17972002 CAAGTGGTGCTCCCACCTCGGCCTCCCAGAATACTGAGACTACAGGTGTGACCCACTGTGCCCAG CAAGTGGTGCTCCCACCTCGGCCTCCCAGAATCCTGAGACTACAGGTGTGACCCACTGTGCCCAG A C MGME1 Ensembl:ENSG00000125871 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1229534038 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14043598 21804 RMVar_ID_21804 Human_SNP_ID_675507495 A-to-I Human chr20 + 17972011 17972011 17972011 CTCCCACCTCGGCCTCCCAGAATACTGAGACTACAGGTGTGACCCACTGTGCCCAGGCAGAATCA CTCCCACCTCGGCCTCCCAGAATACTGAGACTGCAGGTGTGACCCACTGTGCCCAGGCAGAATCA A G MGME1 Ensembl:ENSG00000125871 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs889778022 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14043598 21805 RMVar_ID_21805 Human_SNP_ID_675507722 A-to-I Human chr20 + 17973073 17973073 17973073 TAATGATAGAATTGACATTTCCAGCTGGGCATAGTGGCTCATGCCTGTAATCCTAGCACTTTGGG TAATGATAGAATTGACATTTCCAGCTGGGCATGGTGGCTCATGCCTGTAATCCTAGCACTTTGGG A G MGME1 Ensembl:ENSG00000125871 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs772721474 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14043659 21806 RMVar_ID_21806 Human_SNP_ID_675508098 A-to-I Human chr20 + 17974265 17974265 17974265 TTTTGTATTTTGAGTAGAGACTGGGTTTTACCATGTTGGCCAGGCTGGTCTTGAACTCCTGACCT TTTTGTATTTTGAGTAGAGACTGGGTTTTACCCTGTTGGCCAGGCTGGTCTTGAACTCCTGACCT A C MGME1 Ensembl:ENSG00000125871 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1368572025 Functional Loss SNV dbSNP153 33..33 33 - - - 21807 RMVar_ID_21807 Human_SNP_ID_675508099 A-to-I Human chr20 + 17974265 17974265 17974265 TTTTGTATTTTGAGTAGAGACTGGGTTTTACCATGTTGGCCAGGCTGGTCTTGAACTCCTGACCT TTTTGTATTTTGAGTAGAGACTGGGTTTTACCGTGTTGGCCAGGCTGGTCTTGAACTCCTGACCT A G MGME1 Ensembl:ENSG00000125871 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1368572025 Functional Loss SNV dbSNP153 33..33 33 - - - 21808 RMVar_ID_21808 Human_SNP_ID_675508370 A-to-I Human chr20 + 17975380 17975366 17975380 GGAGTTCGAGACCAGCCTCACCAATATGGTGAAACCCCATCTCTACTAAAAGTAGAAAAATTAGC GGAGTTCGAGACCAGCCTC______________ACCCCATCTCTACTAAAAGTAGAAAAATTAGC CACCAATATGGTGAA C MGME1 Ensembl:ENSG00000125871 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs926963507 Functional Loss DEL dbSNP153 20..33 33 - - - 21809 RMVar_ID_21809 Human_SNP_ID_675508377 A-to-I Human chr20 + 17975397 17975397 17975397 TCACCAATATGGTGAAACCCCATCTCTACTAAAAGTAGAAAAATTAGCCAGGCACGGTGGCGGGC TCACCAATATGGTGAAACCCCATCTCTACTAAGAGTAGAAAAATTAGCCAGGCACGGTGGCGGGC A G MGME1 Ensembl:ENSG00000125871 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1053662870 Functional Loss SNV dbSNP153 33..33 33 - - - 21810 RMVar_ID_21810 Human_SNP_ID_675508797 A-to-I Human chr20 + 17976731 17976731 17976731 TTGCCCAGGCTGGAGTGCAGTGGTGCGATTTCAGCTCACTGCAACCTCCATCTCCTAGGTTCAAG TTGCCCAGGCTGGAGTGCAGTGGTGCGATTTCCGCTCACTGCAACCTCCATCTCCTAGGTTCAAG A C MGME1 Ensembl:ENSG00000125871 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1395625019 Functional Loss SNV dbSNP153 33..33 33 - - - 21811 RMVar_ID_21811 Human_SNP_ID_675508798 A-to-I Human chr20 + 17976731 17976731 17976731 TTGCCCAGGCTGGAGTGCAGTGGTGCGATTTCAGCTCACTGCAACCTCCATCTCCTAGGTTCAAG TTGCCCAGGCTGGAGTGCAGTGGTGCGATTTCGGCTCACTGCAACCTCCATCTCCTAGGTTCAAG A G MGME1 Ensembl:ENSG00000125871 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1395625019 Functional Loss SNV dbSNP153 33..33 33 - - - 21812 RMVar_ID_21812 Human_SNP_ID_675508806 A-to-I Human chr20 + 17976769 17976769 17976769 CTGCAACCTCCATCTCCTAGGTTCAAGCTATTATCTTGCCTCAGCCTCCCAAGTAGCTGGGATTA CTGCAACCTCCATCTCCTAGGTTCAAGCTATTGTCTTGCCTCAGCCTCCCAAGTAGCTGGGATTA A G MGME1 Ensembl:ENSG00000125871 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1306313276 Functional Loss SNV dbSNP153 33..33 33 - - - 21813 RMVar_ID_21813 Human_SNP_ID_675509328 A-to-I Human chr20 + 17978910 17978910 17978910 CAATTCTCCTGTGTCAGCCTCCCCAAGTGGCTAGGACTACAGGCACCCACCACCACGCCTGGCTA CAATTCTCCTGTGTCAGCCTCCCCAAGTGGCTGGGACTACAGGCACCCACCACCACGCCTGGCTA A G MGME1 Ensembl:ENSG00000125871 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1221972426 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14043794 21814 RMVar_ID_21814 Human_SNP_ID_675509330 A-to-I Human chr20 + 17978916 17978916 17978916 TCCTGTGTCAGCCTCCCCAAGTGGCTAGGACTACAGGCACCCACCACCACGCCTGGCTAATTTTT TCCTGTGTCAGCCTCCCCAAGTGGCTAGGACTGCAGGCACCCACCACCACGCCTGGCTAATTTTT A G MGME1 Ensembl:ENSG00000125871 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs540806980 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14043794 21815 RMVar_ID_21815 Human_SNP_ID_675511287 A-to-I Human chr20 + 17986549 17986549 17986549 CTGGCTGATTTTTTGGTATTTTTTATAGAGACAGGGTTTCACCATGTTGCCCAGGCTGGTCTCGG CTGGCTGATTTTTTGGTATTTTTTATAGAGACGGGGTTTCACCATGTTGCCCAGGCTGGTCTCGG A G MGME1 Ensembl:ENSG00000125871 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223271113 Functional Loss SNV dbSNP153 33..33 33 - - - 21816 RMVar_ID_21816 Human_SNP_ID_675511395 A-to-I Human chr20 + 17987055 17987055 17987055 TACAAAAATTAGCTGGGCGAGGTGGCGCACACATGTAATGCCAGCTACTCAGGGGGCTGAGGCAG TACAAAAATTAGCTGGGCGAGGTGGCGCACACGTGTAATGCCAGCTACTCAGGGGGCTGAGGCAG A G MGME1 Ensembl:ENSG00000125871 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1424204288 Functional Loss SNV dbSNP153 33..33 33 - - - 21817 RMVar_ID_21817 Human_SNP_ID_675511397 A-to-I Human chr20 + 17987059 17987059 17987059 AAAATTAGCTGGGCGAGGTGGCGCACACATGTAATGCCAGCTACTCAGGGGGCTGAGGCAGAAGA AAAATTAGCTGGGCGAGGTGGCGCACACATGTGATGCCAGCTACTCAGGGGGCTGAGGCAGAAGA A G MGME1 Ensembl:ENSG00000125871 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1401397612 Functional Loss SNV dbSNP153 33..33 33 - - - 21818 RMVar_ID_21818 Human_SNP_ID_675511418 A-to-I Human chr20 + 17987124 17987124 17987124 ATAGCTTGAACCCAGGAGGCGGAGGTTGTGGTAAGCCGAGATTACACCACTGCACTCCAGCCTGA ATAGCTTGAACCCAGGAGGCGGAGGTTGTGGTCAGCCGAGATTACACCACTGCACTCCAGCCTGA A C MGME1 Ensembl:ENSG00000125871 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1244157955 Functional Loss SNV dbSNP153 33..33 33 - - - 21819 RMVar_ID_21819 Human_SNP_ID_675511954 A-to-I Human chr20 + 17988936 17988936 17988936 ACATAGTGAAACCCCGTATCTACAAAAAAAATACAAAAATTAGCTGGACATGGTGGCGCACACTT ACATAGTGAAACCCCGTATCTACAAAAAAAATTCAAAAATTAGCTGGACATGGTGGCGCACACTT A T MGME1 Ensembl:ENSG00000125871 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs916512221 Functional Loss SNV dbSNP153 33..33 33 - - - 21820 RMVar_ID_21820 Human_SNP_ID_675555659 A-to-I Human chr20 + 18156092 18156092 18156092 AAGGAAGGACATTCTGGCACATGCTGCAGTGTAGATGAACCTTGAGGACATTATGCTGTGTGAAA AAGGAAGGACATTCTGGCACATGCTGCAGTGTGGATGAACCTTGAGGACATTATGCTGTGTGAAA A G KAT14 Ensembl:ENSG00000149474 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049571025 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60223,RMVar_hsa_circ_208889,RMVar_hsa_circ_89025,RMVar_hsa_circ_349153 21821 RMVar_ID_21821 Human_SNP_ID_675591247 A-to-I Human chr20 + 18303164 18303164 18303164 CACCCCCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTTCCAAGTAGCTGGGATTATAGGTGCTGC CACCCCCCAGGTTCAAGCAATTCTCCTGCCTCGGCCTTCCAAGTAGCTGGGATTATAGGTGCTGC A G ZNF133 Ensembl:ENSG00000125846 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs898777433 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80344,RMVar_hsa_circ_125956,RMVar_hsa_circ_208894,RMVar_hsa_circ_76967,RMVar_hsa_circ_208895,RMVar_hsa_circ_208893,RMVar_hsa_circ_280127,RMVar_hsa_circ_368029,RMVar_hsa_circ_208897 21822 RMVar_ID_21822 Human_SNP_ID_675591283 A-to-I Human chr20 + 18303315 18303315 18303315 GTGATCCACCTGCCTCGGCCTCCCAAAGTGCTAGGGTTACAGATGTGAGCCACCGCACCTGGCCA GTGATCCACCTGCCTCGGCCTCCCAAAGTGCTGGGGTTACAGATGTGAGCCACCGCACCTGGCCA A G ZNF133 Ensembl:ENSG00000125846 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256713525 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22722872 RMVar_hsa_circ_80344,RMVar_hsa_circ_125956,RMVar_hsa_circ_208894,RMVar_hsa_circ_76967,RMVar_hsa_circ_208895,RMVar_hsa_circ_208893,RMVar_hsa_circ_280127,RMVar_hsa_circ_368029,RMVar_hsa_circ_208897 21823 RMVar_ID_21823 Human_SNP_ID_675630824 A-to-I Human chr20 + 18472427 18472427 18472427 GCTGGTCTCAAACTCTTGACCTCAAATGGACCACCTGCCTTGACCTCCCAAAGTGCTGAGATTAC GCTGGTCTCAAACTCTTGACCTCAAATGGACCGCCTGCCTTGACCTCCCAAAGTGCTGAGATTAC A G POLR3F Ensembl:ENSG00000132664 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202505912 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3643945,Human_RBP_ID_14044699 RMVar_hsa_circ_23797,RMVar_hsa_circ_332896 21824 RMVar_ID_21824 Human_SNP_ID_675634615 A-to-I Human chr20 - 18487868 18487868 18487868 TCAGCTCACTCTAACCTGCACCTCCCGGGTTCAAGTGATTCTCATCTCAGCCTCCCAAGTAGTGT TCAGCTCACTCTAACCTGCACCTCCCGGGTTCCAGTGATTCTCATCTCAGCCTCCCAAGTAGTGT T G RBBP9 Ensembl:ENSG00000089050 Protein coding 3'UTR GSE38233;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,32596459 RNA-Seq:(High) rs886313746 Functional Loss SNV dbSNP153 33..33 33 - - - 21825 RMVar_ID_21825 Human_SNP_ID_675634744 A-to-I Human chr20 - 18488337 18488337 18488337 TTGAGCCCAGGAGTTTGAGCCTTCAGTGAGCTATGATCGCGCCACTGTACTCCATCCTGGGTGAT TTGAGCCCAGGAGTTTGAGCCTTCAGTGAGCTGTGATCGCGCCACTGTACTCCATCCTGGGTGAT T C RBBP9 Ensembl:ENSG00000089050 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904184708 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4637052,Human_RBP_ID_14044912 21826 RMVar_ID_21826 Human_SNP_ID_675634756 A-to-I Human chr20 - 18488404 18488404 18488404 AACATTAGCTAGGCATGGTGGTGCACACCTGTAGTCCTAGCTTCTTGGGAGGCTGAGGCAGGATT AACATTAGCTAGGCATGGTGGTGCACACCTGTGGTCCTAGCTTCTTGGGAGGCTGAGGCAGGATT T C RBBP9 Ensembl:ENSG00000089050 Protein coding 3'UTR GSE38233;GSE100210;GSE99789;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,29796672,31158229,31158229 RNA-Seq:(High) rs1224999536 Functional Loss SNV dbSNP153 33..33 33 - - - 21827 RMVar_ID_21827 Human_SNP_ID_675634771 A-to-I Human chr20 - 18488462 18488462 18488462 CAGGTGTTTGAGGCCAGCCAGGGCAACACAGCAAGACCCCATCTCTACAAAATATTAAAACATTA CAGGTGTTTGAGGCCAGCCAGGGCAACACAGCGAGACCCCATCTCTACAAAATATTAAAACATTA T C RBBP9 Ensembl:ENSG00000089050 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277073060 Functional Loss SNV dbSNP153 33..33 33 - - - 21828 RMVar_ID_21828 Human_SNP_ID_675634777 A-to-I Human chr20 - 18488493 18488493 18488493 GGGAGGCTGAGGTGGTTGTATTGCTTGAGGCCAGGTGTTTGAGGCCAGCCAGGGCAACACAGCAA GGGAGGCTGAGGTGGTTGTATTGCTTGAGGCCGGGTGTTTGAGGCCAGCCAGGGCAACACAGCAA T C RBBP9 Ensembl:ENSG00000089050 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1009254264 Functional Loss SNV dbSNP153 33..33 33 - - - 21829 RMVar_ID_21829 Human_SNP_ID_675640456 A-to-I Human chr20 + 18509753 18509753 18509753 GGGACTATGGGCACGTGCCACCACACCTGGCTAATTTTTGTATTTTTAGTAGAGACGGAGTTTCA GGGACTATGGGCACGTGCCACCACACCTGGCTCATTTTTGTATTTTTAGTAGAGACGGAGTTTCA A C SEC23B Ensembl:ENSG00000101310 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs960050793 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_208912,RMVar_hsa_circ_86924 21830 RMVar_ID_21830 Human_SNP_ID_675640457 A-to-I Human chr20 + 18509753 18509753 18509753 GGGACTATGGGCACGTGCCACCACACCTGGCTAATTTTTGTATTTTTAGTAGAGACGGAGTTTCA GGGACTATGGGCACGTGCCACCACACCTGGCTGATTTTTGTATTTTTAGTAGAGACGGAGTTTCA A G SEC23B Ensembl:ENSG00000101310 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs960050793 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_208912,RMVar_hsa_circ_86924 21831 RMVar_ID_21831 Human_SNP_ID_675655414 A-to-I Human chr20 + 18569010 18569010 18569010 GTTGGCGAGGCTGGTCTCAAACACCTGACCTCAGGTGGTCCACCTGCCTCGGCCCCCACAAAGTG GTTGGCGAGGCTGGTCTCAAACACCTGACCTCGGGTGGTCCACCTGCCTCGGCCCCCACAAAGTG A G SMIM26,AL121900.1 Ensembl:ENSG00000232388,Ensembl:ENSG00000284776 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1244343138 Functional Loss SNV dbSNP153 33..33 33 - - - 21832 RMVar_ID_21832 Human_SNP_ID_675675436 A-to-I Human chr20 + 18651291 18651291 18651291 CTCCTGCCTCAGCTTCCAGAGTAGCTGGGATTATAGGCATATGCCACCACACTGAGCTAATTTTT CTCCTGCCTCAGCTTCCAGAGTAGCTGGGATTGTAGGCATATGCCACCACACTGAGCTAATTTTT A G DTD1,AL121900.1 Ensembl:ENSG00000125821,Ensembl:ENSG00000284776 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1050030841 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_283630 21833 RMVar_ID_21833 Human_SNP_ID_675843480 A-to-I Human chr20 + 19337359 19337359 19337359 CCAGCTACTCAGGAGGCTGAGACAGGAGAATCACTTGAACCTGGGAGGTGGAGGTTGCGGTGAGC CCAGCTACTCAGGAGGCTGAGACAGGAGAATCGCTTGAACCTGGGAGGTGGAGGTTGCGGTGAGC A G SLC24A3 Ensembl:ENSG00000185052 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1256005296 Functional Loss SNV dbSNP153 33..33 33 - - - 21834 RMVar_ID_21834 Human_SNP_ID_676004756 A-to-I Human chr20 + 19997994 19997994 19997994 CATCCAGATTCACCTGCTTTTTTTTTTTTCTTAAGACAGAGTCTCGCTCTGTCACCCAGGCTGGA CATCCAGATTCACCTGCTTTTTTTTTTTTCTTTAGACAGAGTCTCGCTCTGTCACCCAGGCTGGA A T RIN2 Ensembl:ENSG00000132669 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1160835310 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_208951,RMVar_hsa_circ_110322,RMVar_hsa_circ_208954,RMVar_hsa_circ_91419,RMVar_hsa_circ_104231,RMVar_hsa_circ_208959,RMVar_hsa_circ_208961 21835 RMVar_ID_21835 Human_SNP_ID_676004775 A-to-I Human chr20 + 19998058 19998044 19998059 AGTGCAGTGGTGGCACGATCTCTGCTCACTGCAACCTCCACCTCCCAGGTTCAAACGATTCTCCT AGTGCAGTGGTGGCACGAT_______________CCTCCACCTCCCAGGTTCAAACGATTCTCCT TCTCTGCTCACTGCAA T RIN2 Ensembl:ENSG00000132669 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs779347194 Functional Loss DEL dbSNP153 20..34 33 - - - RMVar_hsa_circ_111672,RMVar_hsa_circ_127553,RMVar_hsa_circ_208947,RMVar_hsa_circ_75817,RMVar_hsa_circ_208949,RMVar_hsa_circ_208951,RMVar_hsa_circ_110322,RMVar_hsa_circ_208954,RMVar_hsa_circ_91419,RMVar_hsa_circ_104231,RMVar_hsa_circ_208959,RMVar_hsa_circ_208961 21836 RMVar_ID_21836 Human_SNP_ID_676004895 A-to-I Human chr20 + 19998536 19998536 19998536 AGGAGGCTAAAGTGGGAGGATCCGTTGAGCCCAGGAGTTTGAGGCTACAGTGAGCCATGATCACA AGGAGGCTAAAGTGGGAGGATCCGTTGAGCCCTGGAGTTTGAGGCTACAGTGAGCCATGATCACA A T RIN2 Ensembl:ENSG00000132669 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1320792399 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_208951,RMVar_hsa_circ_110322,RMVar_hsa_circ_208954,RMVar_hsa_circ_91419,RMVar_hsa_circ_104231,RMVar_hsa_circ_208959,RMVar_hsa_circ_208961 21837 RMVar_ID_21837 Human_SNP_ID_471356018 A-to-I Human chr11 + 70280073 70280073 70280073 GGGACTACAGGTGCGTGCCACCACACCTGGCTAATTTCTGTATTTTCAGTGGAGGTGGGGTTTTG GGGACTACAGGTGCGTGCCACCACACCTGGCTGATTTCTGTATTTTCAGTGGAGGTGGGGTTTTG A G PPFIA1 Ensembl:ENSG00000131626 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277708741 Functional Loss SNV dbSNP153 33..33 33 - - - 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 21838 RMVar_ID_21838 Human_SNP_ID_471363810 A-to-I Human chr11 + 70308864 70308864 70308864 TTGGGAGGCTGAACCTAGGAGTTGGAGGCTGCAGTGAGCTATGATTGTGCCACTTCACTTCAGTC TTGGGAGGCTGAACCTAGGAGTTGGAGGCTGCGGTGAGCTATGATTGTGCCACTTCACTTCAGTC A G PPFIA1 Ensembl:ENSG00000131626 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs566893744 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11698975 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 21839 RMVar_ID_21839 Human_SNP_ID_471380243 A-to-I Human chr11 + 70373354 70373354 70373354 GGCTCAAGTGCTCTTCCTGCCTTAGCCTCCCTAGTAGCTCCTGGGAGTACAGGTGTGCTCCACCA GGCTCAAGTGCTCTTCCTGCCTTAGCCTCCCTGGTAGCTCCTGGGAGTACAGGTGTGCTCCACCA A G PPFIA1 Ensembl:ENSG00000131626 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1014746207 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61701,RMVar_hsa_circ_47213,RMVar_hsa_circ_91345,RMVar_hsa_circ_352348,RMVar_hsa_circ_151383,RMVar_hsa_circ_359947,RMVar_hsa_circ_107953,RMVar_hsa_circ_151384,RMVar_hsa_circ_151386,RMVar_hsa_circ_151385,RMVar_hsa_circ_25307,RMVar_hsa_circ_325214,RMVar_hsa_circ_46129,RMVar_hsa_circ_352326,RMVar_hsa_circ_151392,RMVar_hsa_circ_75239,RMVar_hsa_circ_151395,RMVar_hsa_circ_340677,RMVar_hsa_circ_151394,RMVar_hsa_circ_287399 21840 RMVar_ID_21840 Human_SNP_ID_471380981 A-to-I Human chr11 + 70376209 70376197 70376209 TGGGATTTCACCATGTTGGCCAAGCTGGTCTCAAACTCCTGATCTCAAGTGATCTGCCTGTCTCG TGGGATTTCACCATGTTGGCC____________AACTCCTGATCTCAAGTGATCTGCCTGTCTCG CAAGCTGGTCTCA C PPFIA1 Ensembl:ENSG00000131626 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1424693978 Functional Loss DEL dbSNP153 22..33 33 - - - RMVar_hsa_circ_61701,RMVar_hsa_circ_47213,RMVar_hsa_circ_91345,RMVar_hsa_circ_151383,RMVar_hsa_circ_359947,RMVar_hsa_circ_107953,RMVar_hsa_circ_151384,RMVar_hsa_circ_151385,RMVar_hsa_circ_25307,RMVar_hsa_circ_325214,RMVar_hsa_circ_46129,RMVar_hsa_circ_352326,RMVar_hsa_circ_151392,RMVar_hsa_circ_75239,RMVar_hsa_circ_151395,RMVar_hsa_circ_340677,RMVar_hsa_circ_151394,RMVar_hsa_circ_287399,RMVar_hsa_circ_151396,RMVar_hsa_circ_307928 21841 RMVar_ID_21841 Human_SNP_ID_471388161 A-to-I Human chr11 + 70403461 70403460 70403461 CGCCCGCCTCGGCCTCCGAAAGTGCTGGGATTACAGGCGTGAGCCACCTCACCTGGCCAAGAGTT CGCCCGCCTCGGCCTCCGAAAGTGCTGGGATT_CAGGCGTGAGCCACCTCACCTGGCCAAGAGTT TA T CTTN Ensembl:ENSG00000085733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1052747488 Functional Loss DEL dbSNP153 33..33 33 - - - 21842 RMVar_ID_21842 Human_SNP_ID_471394906 A-to-I Human chr11 + 70426916 70426916 70426916 GCCACTGTGCCCGGCCAAATTTTTTTATCTTTAGTAGAGATGAGGTCTCACTGTGTTGCCCAGGC GCCACTGTGCCCGGCCAAATTTTTTTATCTTTGGTAGAGATGAGGTCTCACTGTGTTGCCCAGGC A G CTTN Ensembl:ENSG00000085733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1014978217 Functional Loss SNV dbSNP153 33..33 33 - - - 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_151411,RMVar_hsa_circ_151412,RMVar_hsa_circ_22373 21843 RMVar_ID_21843 Human_SNP_ID_471750604 A-to-I Human chr11 + 71797596 71797596 71797596 CTCTCATCTCAGCCTCCTGAGTAGCTGGGACTACAGGTGCGTGCTACCACGCCTGGCTAATTTTT CTCTCATCTCAGCCTCCTGAGTAGCTGGGACTGCAGGTGCGTGCTACCACGCCTGGCTAATTTTT A G FAM86C1 Ensembl:ENSG00000158483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs527879993 Functional Loss SNV dbSNP153 33..33 33 - - - 21844 RMVar_ID_21844 Human_SNP_ID_471750605 A-to-I Human chr11 + 71797596 71797596 71797596 CTCTCATCTCAGCCTCCTGAGTAGCTGGGACTACAGGTGCGTGCTACCACGCCTGGCTAATTTTT CTCTCATCTCAGCCTCCTGAGTAGCTGGGACTTCAGGTGCGTGCTACCACGCCTGGCTAATTTTT A T FAM86C1 Ensembl:ENSG00000158483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs527879993 Functional Loss SNV dbSNP153 33..33 33 - - - 21845 RMVar_ID_21845 Human_SNP_ID_471773980 A-to-I Human chr11 - 71880065 71880065 71880065 ATTCCATCATTTATATAATTATACAGAATTATACTTTTCCTCCGTGAATGTTGGTGTTTTATATT ATTCCATCATTTATATAATTATACAGAATTATGCTTTTCCTCCGTGAATGTTGGTGTTTTATATT T C AP002495.1 Ensembl:ENSG00000254469 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs959006567 Functional Loss SNV dbSNP153 33..33 33 - - - 21846 RMVar_ID_21846 Human_SNP_ID_471773981 A-to-I Human chr11 - 71880067 71880067 71880067 AGATTCCATCATTTATATAATTATACAGAATTATACTTTTCCTCCGTGAATGTTGGTGTTTTATA AGATTCCATCATTTATATAATTATACAGAATTGTACTTTTCCTCCGTGAATGTTGGTGTTTTATA T C AP002495.1 Ensembl:ENSG00000254469 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251196042 Functional Loss SNV dbSNP153 33..33 33 - - - 21847 RMVar_ID_21847 Human_SNP_ID_471779258 A-to-I Human chr11 - 71896149 71896139 71896149 TCAGCCCTCCGAGTAGCTGAGACTACAGGCACAGGTCACCACGCCCGACTCATTTTTTGTGTTTA TCAGCCCTCCGAGTAGCTGAGACTACAGGCAC__________GCCCGACTCATTTTTTGTGTTTA CGTGGTGACCT C AP002495.1 Ensembl:ENSG00000254469 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1392952073 Functional Loss DEL dbSNP153 33..42 33 - - - 21848 RMVar_ID_21848 Human_SNP_ID_471779288 A-to-I Human chr11 - 71896216 71896216 71896216 GGTGTACACAGGCACAGTCCGGGCTCACTGCAAGCTCCGCCTCCTGAGTTCAAGCGCTTCTTGGG GGTGTACACAGGCACAGTCCGGGCTCACTGCATGCTCCGCCTCCTGAGTTCAAGCGCTTCTTGGG T A AP002495.1 Ensembl:ENSG00000254469 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1041401108 Functional Loss SNV dbSNP153 33..33 33 - - - 21849 RMVar_ID_21849 Human_SNP_ID_471779289 A-to-I Human chr11 - 71896216 71896216 71896216 GGTGTACACAGGCACAGTCCGGGCTCACTGCAAGCTCCGCCTCCTGAGTTCAAGCGCTTCTTGGG GGTGTACACAGGCACAGTCCGGGCTCACTGCAGGCTCCGCCTCCTGAGTTCAAGCGCTTCTTGGG T C AP002495.1 Ensembl:ENSG00000254469 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1041401108 Functional Loss SNV dbSNP153 33..33 33 - - - 21850 RMVar_ID_21850 Human_SNP_ID_471781171 A-to-I Human chr11 - 71901364 71901364 71901364 TCGAATTACTGACCTTGTGATTCGCCTGCCTCAGCCTCCCAAAGGGCTGGGATTACAGGCGTGAG TCGAATTACTGACCTTGTGATTCGCCTGCCTCCGCCTCCCAAAGGGCTGGGATTACAGGCGTGAG T G AP002495.1 Ensembl:ENSG00000254469 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1450162983 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22709881 21851 RMVar_ID_21851 Human_SNP_ID_471793047 A-to-I Human chr11 + 71942966 71942966 71942966 TGCTGTGTCTTCACATGGCAGAAGGGACACACAGCCTCCCTAAAGCCACTTTTGTAAGGGCACTA TGCTGTGTCTTCACATGGCAGAAGGGACACACGGCCTCCCTAAAGCCACTTTTGTAAGGGCACTA A G RNF121 Ensembl:ENSG00000137522 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10736782 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83685,RMVar_hsa_circ_151476 21852 RMVar_ID_21852 Human_SNP_ID_471797531 A-to-I Human chr11 + 71962109 71962109 71962109 CCTGCCTCGGCTTCCCGCATAGCTGGGACTACAGGTGCCCACCATCACGCCTGACTAATTTTTTT CCTGCCTCGGCTTCCCGCATAGCTGGGACTACGGGTGCCCACCATCACGCCTGACTAATTTTTTT A G RNF121 Ensembl:ENSG00000137522 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs527294602 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83685,RMVar_hsa_circ_151480,RMVar_hsa_circ_275519,RMVar_hsa_circ_348951,RMVar_hsa_circ_151476,RMVar_hsa_circ_312426,RMVar_hsa_circ_151477,RMVar_hsa_circ_376673,RMVar_hsa_circ_305896,RMVar_hsa_circ_151482,RMVar_hsa_circ_151481 21853 RMVar_ID_21853 Human_SNP_ID_471798099 A-to-I Human chr11 + 71964499 71964499 71964499 GGATACCTTTTTTTTTCCTGAGACAAGGTCTTATTCTGATTGCCCATACTGGAATGCAGTGGTGC GGATACCTTTTTTTTTCCTGAGACAAGGTCTTTTTCTGATTGCCCATACTGGAATGCAGTGGTGC A T RNF121 Ensembl:ENSG00000137522 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs566469418 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11702140 RMVar_hsa_circ_83685,RMVar_hsa_circ_275519,RMVar_hsa_circ_348951,RMVar_hsa_circ_151476,RMVar_hsa_circ_312426,RMVar_hsa_circ_151477,RMVar_hsa_circ_376673,RMVar_hsa_circ_151482,RMVar_hsa_circ_151481 21854 RMVar_ID_21854 Human_SNP_ID_471800139 A-to-I Human chr11 + 71973065 71973065 71973065 ACTGTTAGCCGGACATGGTGGTGCATGCCTGTAATCCCAGCTACTCGGAAGGCTGAGGCAGGAGA ACTGTTAGCCGGACATGGTGGTGCATGCCTGTGATCCCAGCTACTCGGAAGGCTGAGGCAGGAGA A G RNF121 Ensembl:ENSG00000137522 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910799310 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83685,RMVar_hsa_circ_275519,RMVar_hsa_circ_348951,RMVar_hsa_circ_151476,RMVar_hsa_circ_312426,RMVar_hsa_circ_151477,RMVar_hsa_circ_376673,RMVar_hsa_circ_151482,RMVar_hsa_circ_151481 21855 RMVar_ID_21855 Human_SNP_ID_471802245 A-to-I Human chr11 + 71982147 71982144 71982148 TCGGGGCCATACCATGGGGGATTTGACAGCCTAGCTAAGAATGTTGGATCCTCTCTACTAAAAAC TCGGGGCCATACCATGGGGGATTTGACAGC____CTAAGAATGTTGGATCCTCTCTACTAAAAAC CCTAG C RNF121 Ensembl:ENSG00000137522 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1374901327 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_11702357 RMVar_hsa_circ_83685,RMVar_hsa_circ_275519,RMVar_hsa_circ_348951,RMVar_hsa_circ_151476,RMVar_hsa_circ_312426,RMVar_hsa_circ_151477,RMVar_hsa_circ_376673,RMVar_hsa_circ_151482,RMVar_hsa_circ_151481 21856 RMVar_ID_21856 Human_SNP_ID_471814628 A-to-I Human chr11 - 72025360 72025360 72025360 TTGCCCAGGCTGGAGTGCAGTGGCATGATCTCAGCTCACTGTAATCTCTGTCGCTTGGGTTGAAG TTGCCCAGGCTGGAGTGCAGTGGCATGATCTCTGCTCACTGTAATCTCTGTCGCTTGGGTTGAAG T A NUMA1 Ensembl:ENSG00000137497 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1386665943 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113356,RMVar_hsa_circ_96395,RMVar_hsa_circ_151495,RMVar_hsa_circ_151496,RMVar_hsa_circ_48545,RMVar_hsa_circ_318563,RMVar_hsa_circ_105870,RMVar_hsa_circ_151497,RMVar_hsa_circ_151498 21857 RMVar_ID_21857 Human_SNP_ID_471820258 A-to-I Human chr11 - 72049491 72049491 72049491 TTGCCCACGCTGGTCTCAAATTCCTTGGCTCAAGTGATCCTCCCATCTTGGCCTCCAAAAGTGCC TTGCCCACGCTGGTCTCAAATTCCTTGGCTCACGTGATCCTCCCATCTTGGCCTCCAAAAGTGCC T G NUMA1 Ensembl:ENSG00000137497 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs572722407 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1272688,Human_Splice_Rec_1272689,Human_Splice_Rec_1272786,Human_Splice_Rec_1272787,Human_Splice_Rec_1272838,Human_Splice_Rec_1272839 RMVar_hsa_circ_113356,RMVar_hsa_circ_151495,RMVar_hsa_circ_3581,RMVar_hsa_circ_45394 21858 RMVar_ID_21858 Human_SNP_ID_471880771 A-to-I Human chr11 - 72286080 72286080 72286080 ATCTCTGCAAAAAATTAGCTGGTTGTGGTGGCATCCACCTGTGGTCTCAGCTACTTGGGAGGCTG ATCTCTGCAAAAAATTAGCTGGTTGTGGTGGCGTCCACCTGTGGTCTCAGCTACTTGGGAGGCTG T C CLPB Ensembl:ENSG00000162129 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs950015163 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4177588 21859 RMVar_ID_21859 Human_SNP_ID_471880975 A-to-I Human chr11 - 72286687 72286687 72286687 AGGTGGATCACCTAGGTCTGGAGTTCGAGACCAGCCTGGACAACATGGTGAAACCCCTCTTTATT AGGTGGATCACCTAGGTCTGGAGTTCGAGACCTGCCTGGACAACATGGTGAAACCCCTCTTTATT T A CLPB Ensembl:ENSG00000162129 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs902028157 Functional Loss SNV dbSNP153 33..33 33 - - - 21860 RMVar_ID_21860 Human_SNP_ID_471881395 A-to-I Human chr11 - 72288483 72288482 72288484 GATTTCTTTTGTTTTGTTTTGTTTTTTGAGACAGAGTCTTGCTCTGTCGCCCAGGCTGGAGTGCG GATTTCTTTTGTTTTGTTTTGTTTTTTGAGA__GAGTCTTGCTCTGTCGCCCAGGCTGGAGTGCG CTG C CLPB Ensembl:ENSG00000162129 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs554464806 Functional Loss DEL dbSNP153 32..33 33 - - - 21861 RMVar_ID_21861 Human_SNP_ID_471881683 A-to-I Human chr11 - 72289731 72289731 72289731 CCTCCAAACGTTTAAAAAATAAAAAATTAGCCAGGCATGGTGGTGCATTCCTGTAATCCTAGCTA CCTCCAAACGTTTAAAAAATAAAAAATTAGCCGGGCATGGTGGTGCATTCCTGTAATCCTAGCTA T C CLPB Ensembl:ENSG00000162129 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1449895315 Functional Loss SNV dbSNP153 33..33 33 - - - 21862 RMVar_ID_21862 Human_SNP_ID_471881712 A-to-I Human chr11 - 72289867 72289867 72289867 ATCTGTATGTTATTAAAAACCGTGAGCCAGGTATGGTGGCTCGTGCCTGTATCCCAGGACTTTGG ATCTGTATGTTATTAAAAACCGTGAGCCAGGTGTGGTGGCTCGTGCCTGTATCCCAGGACTTTGG T C CLPB Ensembl:ENSG00000162129 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs532023434 Functional Loss SNV dbSNP153 33..33 33 - - - 21863 RMVar_ID_21863 Human_SNP_ID_471882088 A-to-I Human chr11 - 72291468 72291468 72291468 CCCTGTCTGTACTAAAAATACAAAAATTAGCCAGGCCCGCTGGTGCCCACCTGTAATCCCAGCTA CCCTGTCTGTACTAAAAATACAAAAATTAGCCGGGCCCGCTGGTGCCCACCTGTAATCCCAGCTA T C CLPB Ensembl:ENSG00000162129 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1000147898 Functional Loss SNV dbSNP153 33..33 33 - - - 21864 RMVar_ID_21864 Human_SNP_ID_471882171 A-to-I Human chr11 - 72291885 72291885 72291885 GTGCCCACCACCACGCCCGGCTACCTTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTAG GTGCCCACCACCACGCCCGGCTACCTTTTTGTGTTTTTAGTAGAGACAGGGTTTCACCATGTTAG T C CLPB Ensembl:ENSG00000162129 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965255375 Functional Loss SNV dbSNP153 33..33 33 - - - 21865 RMVar_ID_21865 Human_SNP_ID_471970568 A-to-I Human chr11 - 72661299 72661299 72661299 ATTTATTTCTGTATTTATTTATTTATTGAGACAGAGTCTTGCTCTGTCACCCAGGCTGGAGGGCA ATTTATTTCTGTATTTATTTATTTATTGAGACGGAGTCTTGCTCTGTCACCCAGGCTGGAGGGCA T C PDE2A Ensembl:ENSG00000186642 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1306978337 Functional Loss SNV dbSNP153 33..33 33 - - - 21866 RMVar_ID_21866 Human_SNP_ID_472007666 A-to-I Human chr11 - 72812150 72812150 72812150 CTTCCACCTCAGTCTCCCGAGTAGCTGAGACTACAGGCACATGCCACTATCGCTGGTTTTGTTGT CTTCCACCTCAGTCTCCCGAGTAGCTGAGACTTCAGGCACATGCCACTATCGCTGGTTTTGTTGT T A AP002381.2 Ensembl:ENSG00000285693 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs931582442 Functional Loss SNV dbSNP153 33..33 33 - - - 21867 RMVar_ID_21867 Human_SNP_ID_472018389 A-to-I Human chr11 - 72852577 72852577 72852577 TCACTGCAACCTTCACCTCCCAGGTTCAAGCAATTCTCGTGCCTCAGCCTCCTGAATAGCTGGGA TCACTGCAACCTTCACCTCCCAGGTTCAAGCAGTTCTCGTGCCTCAGCCTCCTGAATAGCTGGGA T C FCHSD2 Ensembl:ENSG00000137478 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1458003967 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4373,RMVar_hsa_circ_18917,RMVar_hsa_circ_338798,RMVar_hsa_circ_32970,RMVar_hsa_circ_151570,RMVar_hsa_circ_109945,RMVar_hsa_circ_304465,RMVar_hsa_circ_340100,RMVar_hsa_circ_151571,RMVar_hsa_circ_316803,RMVar_hsa_circ_55803,RMVar_hsa_circ_151572,RMVar_hsa_circ_151573,RMVar_hsa_circ_151574 21868 RMVar_ID_21868 Human_SNP_ID_472029668 A-to-I Human chr11 - 72901249 72901249 72901249 GGGGCCACAGGCACGCACCACTGTGCCTGGCTATTTTCTTTGTATTTTCAATAGAGATGGGGGGG GGGGCCACAGGCACGCACCACTGTGCCTGGCTGTTTTCTTTGTATTTTCAATAGAGATGGGGGGG T C FCHSD2 Ensembl:ENSG00000137478 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs377115275 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4373,RMVar_hsa_circ_127751,RMVar_hsa_circ_109945,RMVar_hsa_circ_340100,RMVar_hsa_circ_151571,RMVar_hsa_circ_55803,RMVar_hsa_circ_151578,RMVar_hsa_circ_151572,RMVar_hsa_circ_297389,RMVar_hsa_circ_24262,RMVar_hsa_circ_283103,RMVar_hsa_circ_151579,RMVar_hsa_circ_319778,RMVar_hsa_circ_351999,RMVar_hsa_circ_320676,RMVar_hsa_circ_151581,RMVar_hsa_circ_2597,RMVar_hsa_circ_151583,RMVar_hsa_circ_70183,RMVar_hsa_circ_297220,RMVar_hsa_circ_151584 21869 RMVar_ID_21869 Human_SNP_ID_472060775 A-to-I Human chr11 - 73031354 73031354 73031354 CTCCCACCTCAGCCTCCCGAGTAGCTGGGACTACAGGCACACACCACCACACCAGGCTAATTTTT CTCCCACCTCAGCCTCCCGAGTAGCTGGGACTGCAGGCACACACCACCACACCAGGCTAATTTTT T C FCHSD2 Ensembl:ENSG00000137478 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1370333790 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_151592,RMVar_hsa_circ_30655,RMVar_hsa_circ_282614,RMVar_hsa_circ_151591,RMVar_hsa_circ_151594,RMVar_hsa_circ_275444,RMVar_hsa_circ_63691 21870 RMVar_ID_21870 Human_SNP_ID_472061203 A-to-I Human chr11 - 73033044 73033044 73033044 GACCTCATGATCCGCATGCCTCAGCCCCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCACC GACCTCATGATCCGCATGCCTCAGCCCCCCAAGGTGCTGGGATTACAGGTGTGAGCCACCGCACC T C FCHSD2 Ensembl:ENSG00000137478 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1235782890 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_151592,RMVar_hsa_circ_30655,RMVar_hsa_circ_282614,RMVar_hsa_circ_151591,RMVar_hsa_circ_151594,RMVar_hsa_circ_275444,RMVar_hsa_circ_63691 21871 RMVar_ID_21871 Human_SNP_ID_472072228 A-to-I Human chr11 - 73078833 73078833 73078833 CATGCCTCTAGTCGTAACTACTTGGAGACTGAAGCAGGAGAATCACGTGAGTCCAGGATTTCAAG CATGCCTCTAGTCGTAACTACTTGGAGACTGAGGCAGGAGAATCACGTGAGTCCAGGATTTCAAG T C FCHSD2 Ensembl:ENSG00000137478 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1235305824 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_151592,RMVar_hsa_circ_30655,RMVar_hsa_circ_282614,RMVar_hsa_circ_151594,RMVar_hsa_circ_275444,RMVar_hsa_circ_63691 21872 RMVar_ID_21872 Human_SNP_ID_472072540 A-to-I Human chr11 - 73080127 73080127 73080127 ATACCCGTCTAGTATTTTTATTTTGTAGGGACAGGGTCTTACTATGTTGCCCAGGCTGGTCTCGA ATACCCGTCTAGTATTTTTATTTTGTAGGGACGGGGTCTTACTATGTTGCCCAGGCTGGTCTCGA T C FCHSD2 Ensembl:ENSG00000137478 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1287345309 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_151592,RMVar_hsa_circ_30655,RMVar_hsa_circ_282614,RMVar_hsa_circ_151594,RMVar_hsa_circ_275444,RMVar_hsa_circ_63691 21873 RMVar_ID_21873 Human_SNP_ID_472072740 A-to-I Human chr11 - 73080832 73080832 73080832 TCAAGTGATTCTCCTGCCTCAGCTTCCTGAGTAGCTGGGATTACAGGTGCCTGCCATCACACCTG TCAAGTGATTCTCCTGCCTCAGCTTCCTGAGTTGCTGGGATTACAGGTGCCTGCCATCACACCTG T A FCHSD2 Ensembl:ENSG00000137478 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs188839453 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_151592,RMVar_hsa_circ_30655,RMVar_hsa_circ_282614,RMVar_hsa_circ_151594,RMVar_hsa_circ_275444,RMVar_hsa_circ_63691 21874 RMVar_ID_21874 Human_SNP_ID_472072855 A-to-I Human chr11 - 73081339 73081339 73081339 CCCTCCACCTCCCAAGTTCAAGCAATTCTCCTACCTCATCCTCCCGAATAGCTGGGACTACAGGT CCCTCCACCTCCCAAGTTCAAGCAATTCTCCTGCCTCATCCTCCCGAATAGCTGGGACTACAGGT T C FCHSD2 Ensembl:ENSG00000137478 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1373741084 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_151592,RMVar_hsa_circ_30655,RMVar_hsa_circ_282614,RMVar_hsa_circ_151594,RMVar_hsa_circ_275444,RMVar_hsa_circ_63691 21875 RMVar_ID_21875 Human_SNP_ID_472072856 A-to-I Human chr11 - 73081339 73081339 73081339 CCCTCCACCTCCCAAGTTCAAGCAATTCTCCTACCTCATCCTCCCGAATAGCTGGGACTACAGGT CCCTCCACCTCCCAAGTTCAAGCAATTCTCCTCCCTCATCCTCCCGAATAGCTGGGACTACAGGT T G FCHSD2 Ensembl:ENSG00000137478 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1373741084 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_151592,RMVar_hsa_circ_30655,RMVar_hsa_circ_282614,RMVar_hsa_circ_151594,RMVar_hsa_circ_275444,RMVar_hsa_circ_63691 21876 RMVar_ID_21876 Human_SNP_ID_472072933 A-to-I Human chr11 - 73081590 73081590 73081590 CCCTGGAGCCGGAGATTGCAGTGAGCTCAGATAGTGCCATTGGACTCCAGCCTGGGCAATGGGAG CCCTGGAGCCGGAGATTGCAGTGAGCTCAGATGGTGCCATTGGACTCCAGCCTGGGCAATGGGAG T C FCHSD2 Ensembl:ENSG00000137478 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs960777669 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_151592,RMVar_hsa_circ_30655,RMVar_hsa_circ_282614,RMVar_hsa_circ_151594,RMVar_hsa_circ_275444,RMVar_hsa_circ_63691 21877 RMVar_ID_21877 Human_SNP_ID_472084457 A-to-I Human chr11 - 73129995 73129995 73129995 GTGCCTGGAGTCCCAGCTACTCGGTGGGGGCTAAGGCAGGAGAATGACGTGAACCCGGGAGGCAG GTGCCTGGAGTCCCAGCTACTCGGTGGGGGCTGAGGCAGGAGAATGACGTGAACCCGGGAGGCAG T C FCHSD2 Ensembl:ENSG00000137478 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1203614381 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63691 21878 RMVar_ID_21878 Human_SNP_ID_472126736 A-to-I Human chr11 + 73298612 73298612 73298612 CACAGTAAGACCCTGTTTCTACAAAAAAATATAAAAAATAGCCTGGTGTGGTGGTGTCTGACTGT CACAGTAAGACCCTGTTTCTACAAAAAAATATTAAAAATAGCCTGGTGTGGTGGTGTCTGACTGT A T P2RY6 Ensembl:ENSG00000171631 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs926057798 Functional Loss SNV dbSNP153 33..33 33 - - - 21879 RMVar_ID_21879 Human_SNP_ID_472127867 A-to-I Human chr11 + 73303405 73303405 73303405 GAAAGGAAACACAAGGCCAGGCGTGGTGGCTCATGCCTGTAATCCTAGCATTTTGGGAGGCTGAG GAAAGGAAACACAAGGCCAGGCGTGGTGGCTCTTGCCTGTAATCCTAGCATTTTGGGAGGCTGAG A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs953266156 Functional Loss SNV dbSNP153 33..33 33 - - - 21880 RMVar_ID_21880 Human_SNP_ID_472137483 A-to-I Human chr11 + 73337519 73337519 73337519 CAGCTCATTGTAGCCTTGACATCCCAGAGCTCAAGTGATCCTCCTACTTCAGCCTCCTGAGTAGC CAGCTCATTGTAGCCTTGACATCCCAGAGCTCCAGTGATCCTCCTACTTCAGCCTCCTGAGTAGC A C ARHGEF17 Ensembl:ENSG00000110237 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1421611872 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269817,RMVar_hsa_circ_269484 21881 RMVar_ID_21881 Human_SNP_ID_472152894 A-to-I Human chr11 - 73395135 73395135 73395135 GAGGGCCCAGCCTCCGTGATGGTCTTCACCTCAGACACCATTGAACTTGTCCGCTGCTCAGGAAT GAGGGCCCAGCCTCCGTGATGGTCTTCACCTCGGACACCATTGAACTTGTCCGCTGCTCAGGAAT T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs757144421 Functional Loss SNV dbSNP153 33..33 33 - - - 21882 RMVar_ID_21882 Human_SNP_ID_472155424 A-to-I Human chr11 - 73405003 73405003 73405003 AGAGGGACCCCTGGGACGAGGAGGTCCCTGCTAGTCTCAGCCAGGAGCCTGGATTGCCCAGCAGC AGAGGGACCCCTGGGACGAGGAGGTCCCTGCTTGTCTCAGCCAGGAGCCTGGATTGCCCAGCAGC T A FAM168A Ensembl:ENSG00000054965 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1565230444 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4178100,Human_RBP_ID_6092448,Human_RBP_ID_8175259,Human_RBP_ID_8771732,Human_RBP_ID_17682599,Human_RBP_ID_17800885 21883 RMVar_ID_21883 Human_SNP_ID_472173157 A-to-I Human chr11 - 73484583 73484558 73484584 ATATATCGATATAGATATCGATATATAGATAGATATCGATATATAGATATATAGATATATAGATA ATATATCGATATAGATATCGATATATAGATA__________________________TATAGATA ATATCTATATATCTATATATCGATATC A FAM168A Ensembl:ENSG00000054965 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1243756685 Functional Loss DEL dbSNP153 32..57 33 - - - RMVar_hsa_circ_112062,RMVar_hsa_circ_151612 21884 RMVar_ID_21884 Human_SNP_ID_472173165 A-to-I Human chr11 - 73484583 73484566 73484584 ATATATCGATATAGATATCGATATATAGATAGATATCGATATATAGATATATAGATATATAGATA ATATATCGATATAGATATCGATATATAGATA__________________TATAGATATATAGATA ATATCTATATATCGATATC A FAM168A Ensembl:ENSG00000054965 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1383077578 Functional Loss DEL dbSNP153 32..49 33 - - - RMVar_hsa_circ_112062,RMVar_hsa_circ_151612 21885 RMVar_ID_21885 Human_SNP_ID_472173181 A-to-I Human chr11 - 73484583 73484574 73484584 ATATATCGATATAGATATCGATATATAGATAGATATCGATATATAGATATATAGATATATAGATA ATATATCGATATAGATATCGATATATAGATA__________TATAGATATATAGATATATAGATA ATATCGATATC A FAM168A Ensembl:ENSG00000054965 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs372583481 Functional Loss DEL dbSNP153 32..41 33 - - - RMVar_hsa_circ_112062,RMVar_hsa_circ_151612 21886 RMVar_ID_21886 Human_SNP_ID_472173183 A-to-I Human chr11 - 73484583 73484576 73484584 ATATATCGATATAGATATCGATATATAGATAGATATCGATATATAGATATATAGATATATAGATA ATATATCGATATAGATATCGATATATAGATA________TATATAGATATATAGATATATAGATA ATCGATATC A FAM168A Ensembl:ENSG00000054965 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs768530949 Functional Loss DEL dbSNP153 32..39 33 - - - RMVar_hsa_circ_112062,RMVar_hsa_circ_151612 21887 RMVar_ID_21887 Human_SNP_ID_472173193 A-to-I Human chr11 - 73484583 73484580 73484584 ATATATCGATATAGATATCGATATATAGATAGATATCGATATATAGATATATAGATATATAGATA ATATATCGATATAGATATCGATATATAGATA____TCGATATATAGATATATAGATATATAGATA ATATC A FAM168A Ensembl:ENSG00000054965 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs539276904 Functional Loss DEL dbSNP153 32..35 33 - - - RMVar_hsa_circ_112062,RMVar_hsa_circ_151612 21888 RMVar_ID_21888 Human_SNP_ID_472173194 A-to-I Human chr11 - 73484583 73484581 73484584 ATATATCGATATAGATATCGATATATAGATAGATATCGATATATAGATATATAGATATATAGATA ATATATCGATATAGATATCGATATATAGATA___ATCGATATATAGATATATAGATATATAGATA TATC T FAM168A Ensembl:ENSG00000054965 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs976676061 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_112062,RMVar_hsa_circ_151612 21889 RMVar_ID_21889 Human_SNP_ID_472173198 A-to-I Human chr11 - 73484589 73484584 73484590 ATAGATATATATCGATATAGATATCGATATATAGATAGATATCGATATATAGATATATAGATATA ATAGATATATATCGATATAGATATCGATATA______GATATCGATATATAGATATATAGATATA CTATCTA C FAM168A Ensembl:ENSG00000054965 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1300746751 Functional Loss DEL dbSNP153 32..37 33 - - - RMVar_hsa_circ_112062,RMVar_hsa_circ_151612 21890 RMVar_ID_21890 Human_SNP_ID_472179266 A-to-I Human chr11 - 73510684 73510684 73510684 TTTTTTCCGGAGTAATAAGTTACAATATGGGAAATTATTCCGAATCCTGGTAGGATGTACCCCCT TTTTTTCCGGAGTAATAAGTTACAATATGGGAGATTATTCCGAATCCTGGTAGGATGTACCCCCT T C FAM168A Ensembl:ENSG00000054965 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs76687648 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112062,RMVar_hsa_circ_151612 21891 RMVar_ID_21891 Human_SNP_ID_472179270 A-to-I Human chr11 - 73510702 73510702 73510702 ATATATCCAAATGGTTCTTTTTTTCCGGAGTAATAAGTTACAATATGGGAAATTATTCCGAATCC ATATATCCAAATGGTTCTTTTTTTCCGGAGTAGTAAGTTACAATATGGGAAATTATTCCGAATCC T C FAM168A Ensembl:ENSG00000054965 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs78488218 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112062,RMVar_hsa_circ_151612 21892 RMVar_ID_21892 Human_SNP_ID_472219146 A-to-I Human chr11 - 73678570 73678570 73678570 TTCTGTCGCCCAGGCTGGAGTGCAGCAGCGCAATCTCAGCTCACCACAACCTCTGCCTCCTGAAT TTCTGTCGCCCAGGCTGGAGTGCAGCAGCGCAGTCTCAGCTCACCACAACCTCTGCCTCCTGAAT T C RAB6A Ensembl:ENSG00000175582 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs778995892 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125500,RMVar_hsa_circ_378649,RMVar_hsa_circ_151619,RMVar_hsa_circ_151620 21893 RMVar_ID_21893 Human_SNP_ID_472219278 A-to-I Human chr11 - 73678901 73678901 73678901 ACCAACATGGAGAAACCTTGTCTCTACTAAAAATAAAAAAATTACCTGGGCGTGATAGTGCACGC ACCAACATGGAGAAACCTTGTCTCTACTAAAATTAAAAAAATTACCTGGGCGTGATAGTGCACGC T A RAB6A Ensembl:ENSG00000175582 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1374504630 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125500,RMVar_hsa_circ_378649,RMVar_hsa_circ_151619,RMVar_hsa_circ_151620 21894 RMVar_ID_21894 Human_SNP_ID_472219279 A-to-I Human chr11 - 73678901 73678901 73678901 ACCAACATGGAGAAACCTTGTCTCTACTAAAAATAAAAAAATTACCTGGGCGTGATAGTGCACGC ACCAACATGGAGAAACCTTGTCTCTACTAAAAGTAAAAAAATTACCTGGGCGTGATAGTGCACGC T C RAB6A Ensembl:ENSG00000175582 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1374504630 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125500,RMVar_hsa_circ_378649,RMVar_hsa_circ_151619,RMVar_hsa_circ_151620 21895 RMVar_ID_21895 Human_SNP_ID_472221341 A-to-I Human chr11 - 73686361 73686361 73686361 TTAGTAGAGATGGAGTTTCACCATGTTGGCCAAGCTGGTCGAACTCCTGACCTCAAATGATCCCC TTAGTAGAGATGGAGTTTCACCATGTTGGCCACGCTGGTCGAACTCCTGACCTCAAATGATCCCC T G RAB6A Ensembl:ENSG00000175582 Protein coding intron GSE100210;GSE107867;GSE107867 HepG2 cell line;ASD brains,frontal_cortex;ASD brains,temporal_cortex - 29129909,30559470,30559470 RNA-Seq:(High) rs1173713390 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95208,RMVar_hsa_circ_125500,RMVar_hsa_circ_378649,RMVar_hsa_circ_151619,RMVar_hsa_circ_151620,RMVar_hsa_circ_269193,RMVar_hsa_circ_151621 21896 RMVar_ID_21896 Human_SNP_ID_472223630 A-to-I Human chr11 - 73694655 73694655 73694655 ATTCCCAGGCTGATCTCGAACTTCTGGGCCCAAGTGATCATCCCATCTTGGCCTCCCAAAGTGCT ATTCCCAGGCTGATCTCGAACTTCTGGGCCCAGGTGATCATCCCATCTTGGCCTCCCAAAGTGCT T C RAB6A Ensembl:ENSG00000175582 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1021150193 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95208,RMVar_hsa_circ_125500,RMVar_hsa_circ_378649,RMVar_hsa_circ_151619,RMVar_hsa_circ_151620,RMVar_hsa_circ_269193,RMVar_hsa_circ_151621 21897 RMVar_ID_21897 Human_SNP_ID_472224209 A-to-I Human chr11 - 73696877 73696877 73696877 AATCAGGCCAGGCACGATGGCTCATGCCCGGTAATCCCAGCACCTTGGGAGGCCAAGGTGGGAGG AATCAGGCCAGGCACGATGGCTCATGCCCGGTTATCCCAGCACCTTGGGAGGCCAAGGTGGGAGG T A RAB6A Ensembl:ENSG00000175582 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1412702634 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95208,RMVar_hsa_circ_125500,RMVar_hsa_circ_378649,RMVar_hsa_circ_151619,RMVar_hsa_circ_151620,RMVar_hsa_circ_269193,RMVar_hsa_circ_151621 21898 RMVar_ID_21898 Human_SNP_ID_472226049 A-to-I Human chr11 - 73704171 73704171 73704171 TGCCATGTTGCCCAGGCTAGTCTTGAACTCCTAGACTCAGGTGATCCTCCCAACTTGGCCTCGAA TGCCATGTTGCCCAGGCTAGTCTTGAACTCCTGGACTCAGGTGATCCTCCCAACTTGGCCTCGAA T C RAB6A Ensembl:ENSG00000175582 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1343614337 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11708068 Human_Splice_Rec_1276578 RMVar_hsa_circ_95208,RMVar_hsa_circ_125500,RMVar_hsa_circ_378649,RMVar_hsa_circ_151619,RMVar_hsa_circ_151620,RMVar_hsa_circ_269193,RMVar_hsa_circ_151621 21899 RMVar_ID_21899 Human_SNP_ID_472229223 A-to-I Human chr11 - 73714550 73714550 73714550 TCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACTGATGCCTGCCACCATGCCCG TCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTGGCTGGGATTACTGATGCCTGCCACCATGCCCG T C RAB6A Ensembl:ENSG00000175582 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs920407818 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_151626,RMVar_hsa_circ_95208,RMVar_hsa_circ_125500,RMVar_hsa_circ_378649,RMVar_hsa_circ_151619,RMVar_hsa_circ_151620,RMVar_hsa_circ_269193,RMVar_hsa_circ_127239,RMVar_hsa_circ_289612,RMVar_hsa_circ_151622,RMVar_hsa_circ_151621,RMVar_hsa_circ_291498,RMVar_hsa_circ_283163,RMVar_hsa_circ_288091,RMVar_hsa_circ_276496,RMVar_hsa_circ_151628,RMVar_hsa_circ_151627,RMVar_hsa_circ_151624,RMVar_hsa_circ_151625,RMVar_hsa_circ_151623 21900 RMVar_ID_21900 Human_SNP_ID_472235829 A-to-I Human chr11 - 73737414 73737414 73737414 CAGTGGTGTGATCATAGCTCACTGCAGCCTCAAACTCCTAGGTTCAAGCAATCCTTCTGCTTCGG CAGTGGTGTGATCATAGCTCACTGCAGCCTCAGACTCCTAGGTTCAAGCAATCCTTCTGCTTCGG T C RAB6A Ensembl:ENSG00000175582 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs537636994 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127239,RMVar_hsa_circ_93443,RMVar_hsa_circ_151623,RMVar_hsa_circ_151633 21901 RMVar_ID_21901 Human_SNP_ID_472239712 A-to-I Human chr11 - 73750496 73750496 73750496 CAAAAATTTGCTGGGCGCGGTGGCACATGCCTATAATCCCAGCTGCCCTGGAGACTGAGGCACGA CAAAAATTTGCTGGGCGCGGTGGCACATGCCTGTAATCCCAGCTGCCCTGGAGACTGAGGCACGA T C RAB6A Ensembl:ENSG00000175582 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1297251917 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127239,RMVar_hsa_circ_93443,RMVar_hsa_circ_151623,RMVar_hsa_circ_151633 21902 RMVar_ID_21902 Human_SNP_ID_472250027 A-to-I Human chr11 + 73787988 73787987 73787988 CGCGCAGCAGCAAAGGATGAGCGGAACCTTGGAAAAGGTAACGTAGATTCCACGCACGCGGGGCG CGCGCAGCAGCAAAGGATGAGCGGAACCTTGG_AAAGGTAACGTAGATTCCACGCACGCGGGGCG GA G MRPL48 Ensembl:ENSG00000175581 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs768737589 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_1460203,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 21903 RMVar_ID_21903 Human_SNP_ID_472250028 A-to-I Human chr11 + 73787988 73787988 73787988 CGCGCAGCAGCAAAGGATGAGCGGAACCTTGGAAAAGGTAACGTAGATTCCACGCACGCGGGGCG CGCGCAGCAGCAAAGGATGAGCGGAACCTTGGGAAAGGTAACGTAGATTCCACGCACGCGGGGCG A G MRPL48 Ensembl:ENSG00000175581 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs17850551 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1460203,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 21904 RMVar_ID_21904 Human_SNP_ID_472258591 A-to-I Human chr11 + 73823757 73823757 73823757 TATTTGCACTACAACCTCAAACTCCTAGTCTCAAGCAATCCTCCTGCCTCAGCCTCCTGAGTAGC TATTTGCACTACAACCTCAAACTCCTAGTCTCGAGCAATCCTCCTGCCTCAGCCTCCTGAGTAGC A G MRPL48 Ensembl:ENSG00000175581 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1464915014 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_151639,RMVar_hsa_circ_113386,RMVar_hsa_circ_375635,RMVar_hsa_circ_151638 21905 RMVar_ID_21905 Human_SNP_ID_472258813 A-to-I Human chr11 + 73824569 73824569 73824569 ATCGCACCACTGCACTCCAACCTGGGTTACAGAATGAGACTCTATCTCAAAAAAAAAAACAAAAA ATCGCACCACTGCACTCCAACCTGGGTTACAGGATGAGACTCTATCTCAAAAAAAAAAACAAAAA A G MRPL48 Ensembl:ENSG00000175581 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1253063551 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_151639,RMVar_hsa_circ_113386,RMVar_hsa_circ_375635,RMVar_hsa_circ_151638 21906 RMVar_ID_21906 Human_SNP_ID_472260963 A-to-I Human chr11 - 73833721 73833721 73833721 ACAGTGTGCTATGATTGCACCACTGCACTCCAACCTGGGCAACAGAGCAAGACCCTGTCTCTGAA ACAGTGTGCTATGATTGCACCACTGCACTCCAGCCTGGGCAACAGAGCAAGACCCTGTCTCTGAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1312646255 Functional Loss SNV dbSNP153 33..33 33 - - - 21907 RMVar_ID_21907 Human_SNP_ID_472262437 A-to-I Human chr11 + 73840235 73840235 73840235 TAAAAGGGGGCTGGAAGCTGTGGCTTATGCCTATAATCCTAATACTTTGGGAGGCCAAGGCTGGC TAAAAGGGGGCTGGAAGCTGTGGCTTATGCCTGTAATCCTAATACTTTGGGAGGCCAAGGCTGGC A G MRPL48 Ensembl:ENSG00000175581 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042134186 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_280487,RMVar_hsa_circ_151639,RMVar_hsa_circ_113386,RMVar_hsa_circ_375635,RMVar_hsa_circ_151638,RMVar_hsa_circ_364742 21908 RMVar_ID_21908 Human_SNP_ID_472262485 A-to-I Human chr11 + 73840409 73840409 73840409 CTAGCTGCTCAGGAGGTTGAGGTGTGACGATCACTTGAGCCTAGGAGGTCGAGGCTGCAGTAAGC CTAGCTGCTCAGGAGGTTGAGGTGTGACGATCGCTTGAGCCTAGGAGGTCGAGGCTGCAGTAAGC A G MRPL48 Ensembl:ENSG00000175581 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1327592914 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_280487,RMVar_hsa_circ_151639,RMVar_hsa_circ_113386,RMVar_hsa_circ_375635,RMVar_hsa_circ_151638,RMVar_hsa_circ_364742 21909 RMVar_ID_21909 Human_SNP_ID_472262487 A-to-I Human chr11 + 73840419 73840419 73840419 AGGAGGTTGAGGTGTGACGATCACTTGAGCCTAGGAGGTCGAGGCTGCAGTAAGCTGTGATTGTG AGGAGGTTGAGGTGTGACGATCACTTGAGCCTCGGAGGTCGAGGCTGCAGTAAGCTGTGATTGTG A C MRPL48 Ensembl:ENSG00000175581 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1026804777 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_280487,RMVar_hsa_circ_151639,RMVar_hsa_circ_113386,RMVar_hsa_circ_375635,RMVar_hsa_circ_151638,RMVar_hsa_circ_364742 21910 RMVar_ID_21910 Human_SNP_ID_472262948 A-to-I Human chr11 + 73842598 73842598 73842598 GGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCAAGCAGCTGGGACTACAGGCGCACACCACCGTG GGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCGAGCAGCTGGGACTACAGGCGCACACCACCGTG A G MRPL48 Ensembl:ENSG00000175581 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1430107378 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_280487,RMVar_hsa_circ_151639,RMVar_hsa_circ_113386,RMVar_hsa_circ_375635,RMVar_hsa_circ_151638,RMVar_hsa_circ_364742 21911 RMVar_ID_21911 Human_SNP_ID_472269940 A-to-I Human chr11 - 73873676 73873676 73873676 TGTCTCTATTAAAGAATCAAAAAAATTAGCTGAGTGGTGATGCACACCTGTAGTCCCAGCTACTC TGTCTCTATTAAAGAATCAAAAAAATTAGCTGGGTGGTGATGCACACCTGTAGTCCCAGCTACTC T C COA4 Ensembl:ENSG00000181924 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs3210738 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17560094,Human_RBP_ID_17800975 21912 RMVar_ID_21912 Human_SNP_ID_472270179 A-to-I Human chr11 - 73874823 73874823 73874823 TGCCATCACGCCCGCCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCATCATCCCGGCCAGGC TGCCATCACGCCCGCCTAATTTTTGTATTTTTGGTAGAGACGGGGTTTCATCATCCCGGCCAGGC T C COA4 Ensembl:ENSG00000181924 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1029901353 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11709467 21913 RMVar_ID_21913 Human_SNP_ID_472271415 A-to-I Human chr11 + 73879736 73879736 73879736 TCTATAAAAAACAAAAAAAATTAGTCAGGCATAGTGGCATGCGCATGTAGTCCCAGCTACTTGGG TCTATAAAAAACAAAAAAAATTAGTCAGGCATGGTGGCATGCGCATGTAGTCCCAGCTACTTGGG A G PAAF1 Ensembl:ENSG00000175575 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1394861437 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26667,RMVar_hsa_circ_103792,RMVar_hsa_circ_151644 21914 RMVar_ID_21914 Human_SNP_ID_472271496 A-to-I Human chr11 + 73880042 73880042 73880042 GGAGGATTGCTTGAGACCAGCCTGGGAGACATAGGGAGACCTCGTGTCTACAGCAAATAAAACTA GGAGGATTGCTTGAGACCAGCCTGGGAGACATCGGGAGACCTCGTGTCTACAGCAAATAAAACTA A C PAAF1 Ensembl:ENSG00000175575 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1391544082 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26667,RMVar_hsa_circ_103792,RMVar_hsa_circ_151644 21915 RMVar_ID_21915 Human_SNP_ID_472271635 A-to-I Human chr11 + 73880566 73880566 73880566 AAAATTAGCCGGATGTGGTGGTGGGCCCCTGTAGTCCCAGCTACTCGGGAGCCTGAGGCAGGAGA AAAATTAGCCGGATGTGGTGGTGGGCCCCTGTGGTCCCAGCTACTCGGGAGCCTGAGGCAGGAGA A G PAAF1 Ensembl:ENSG00000175575 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1132819 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26667,RMVar_hsa_circ_103792,RMVar_hsa_circ_151644 21916 RMVar_ID_21916 Human_SNP_ID_472271878 A-to-I Human chr11 + 73881312 73881312 73881312 TACATACTATTAAAGCAGTATTTTTTAAACAGAATCTAGCTCTGTCACCTAGGCTGGAATGCAGT TACATACTATTAAAGCAGTATTTTTTAAACAGCATCTAGCTCTGTCACCTAGGCTGGAATGCAGT A C PAAF1 Ensembl:ENSG00000175575 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1031294061 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26667,RMVar_hsa_circ_103792,RMVar_hsa_circ_151644 21917 RMVar_ID_21917 Human_SNP_ID_472272344 A-to-I Human chr11 + 73883101 73883101 73883101 TTTTAAATTTTTTGTAGAGACAAGGTCTCACTATGTTGCCCAGGCTGGTCTTGAACTCCTGTGTT TTTTAAATTTTTTGTAGAGACAAGGTCTCACTCTGTTGCCCAGGCTGGTCTTGAACTCCTGTGTT A C PAAF1 Ensembl:ENSG00000175575 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs183630096 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26667,RMVar_hsa_circ_103792,RMVar_hsa_circ_151644 21918 RMVar_ID_21918 Human_SNP_ID_472272345 A-to-I Human chr11 + 73883101 73883101 73883101 TTTTAAATTTTTTGTAGAGACAAGGTCTCACTATGTTGCCCAGGCTGGTCTTGAACTCCTGTGTT TTTTAAATTTTTTGTAGAGACAAGGTCTCACTGTGTTGCCCAGGCTGGTCTTGAACTCCTGTGTT A G PAAF1 Ensembl:ENSG00000175575 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs183630096 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26667,RMVar_hsa_circ_103792,RMVar_hsa_circ_151644 21919 RMVar_ID_21919 Human_SNP_ID_472272897 A-to-I Human chr11 + 73885595 73885595 73885595 TGGTCGTGGTGGCTCACACCTGTAATCCCAGCACTTCGGGAGGTTGAGGTGGGTGGATCACCTGA TGGTCGTGGTGGCTCACACCTGTAATCCCAGCCCTTCGGGAGGTTGAGGTGGGTGGATCACCTGA A C PAAF1 Ensembl:ENSG00000175575 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1165662143 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26667,RMVar_hsa_circ_103792,RMVar_hsa_circ_151644 21920 RMVar_ID_21920 Human_SNP_ID_472280240 A-to-I Human chr11 + 73914926 73914916 73914927 CGGGGTTTCACCATGTTGGCCAGACTAGTCTCAAACTCCTGACTCAAGTGATCCGCCTGCCTCAA CGGGGTTTCACCATGTTGGCCAG___________ACTCCTGACTCAAGTGATCCGCCTGCCTCAA GACTAGTCTCAA G PAAF1 Ensembl:ENSG00000175575 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs918412554 Functional Loss DEL dbSNP153 24..34 33 - - - RMVar_hsa_circ_103792,RMVar_hsa_circ_85233,RMVar_hsa_circ_340507,RMVar_hsa_circ_151644,RMVar_hsa_circ_357320,RMVar_hsa_circ_282335,RMVar_hsa_circ_51042,RMVar_hsa_circ_151646,RMVar_hsa_circ_151647,RMVar_hsa_circ_34755 21921 RMVar_ID_21921 Human_SNP_ID_472280357 A-to-I Human chr11 + 73915439 73915438 73915439 GACTGGCCTGGGCAAAAAAACCCATCTCTATTAAAAATACAAAAAATTGGCTGGGCATGGTGGCA GACTGGCCTGGGCAAAAAAACCCATCTCTATT_AAAATACAAAAAATTGGCTGGGCATGGTGGCA TA T PAAF1 Ensembl:ENSG00000175575 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1051055793 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_103792,RMVar_hsa_circ_85233,RMVar_hsa_circ_340507,RMVar_hsa_circ_151644,RMVar_hsa_circ_357320,RMVar_hsa_circ_282335,RMVar_hsa_circ_51042,RMVar_hsa_circ_151646,RMVar_hsa_circ_151647,RMVar_hsa_circ_34755 21922 RMVar_ID_21922 Human_SNP_ID_472283258 A-to-I Human chr11 - 73927629 73927629 73927629 TAACAAAACTGGTTTAAGAACAAACTAAAAGCATCTATATCCTTGCCCTGTGTTGCTGGGGTGAG TAACAAAACTGGTTTAAGAACAAACTAAAAGCTTCTATATCCTTGCCCTGTGTTGCTGGGGTGAG T A - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs558293529 Functional Loss SNV dbSNP153 33..33 33 - - - 21923 RMVar_ID_21923 Human_SNP_ID_472283259 A-to-I Human chr11 - 73927629 73927629 73927629 TAACAAAACTGGTTTAAGAACAAACTAAAAGCATCTATATCCTTGCCCTGTGTTGCTGGGGTGAG TAACAAAACTGGTTTAAGAACAAACTAAAAGCGTCTATATCCTTGCCCTGTGTTGCTGGGGTGAG T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs558293529 Functional Loss SNV dbSNP153 33..33 33 - - - 21924 RMVar_ID_21924 Human_SNP_ID_472292275 A-to-I Human chr11 - 73963250 73963250 73963250 ACCTCCACCTCCTCGGTTCAAGCGATTCTCCTACCTCAGCCTCCTAAGTGGCTGGGATTGCAGGC ACCTCCACCTCCTCGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTAAGTGGCTGGGATTGCAGGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1271482385 Functional Loss SNV dbSNP153 33..33 33 - - - 21925 RMVar_ID_21925 Human_SNP_ID_472334035 A-to-I Human chr11 - 74130304 74130304 74130304 GGAGGATTACTTGAGCCCAGGAGTTCAAGGATACAATGAGCTAGGATTACACCACCGTATTCCAG GGAGGATTACTTGAGCCCAGGAGTTCAAGGATGCAATGAGCTAGGATTACACCACCGTATTCCAG T C C2CD3 Ensembl:ENSG00000168014 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1326556818 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6301,RMVar_hsa_circ_100073,RMVar_hsa_circ_113937,RMVar_hsa_circ_151665,RMVar_hsa_circ_78234,RMVar_hsa_circ_151664,RMVar_hsa_circ_92577,RMVar_hsa_circ_151666,RMVar_hsa_circ_151669,RMVar_hsa_circ_113843,RMVar_hsa_circ_151675,RMVar_hsa_circ_70342,RMVar_hsa_circ_97222,RMVar_hsa_circ_120544,RMVar_hsa_circ_94654,RMVar_hsa_circ_151681,RMVar_hsa_circ_151680,RMVar_hsa_circ_151683,RMVar_hsa_circ_104999,RMVar_hsa_circ_151684,RMVar_hsa_circ_85820,RMVar_hsa_circ_367622,RMVar_hsa_circ_151686,RMVar_hsa_circ_122885,RMVar_hsa_circ_151693,RMVar_hsa_circ_8871,RMVar_hsa_circ_151689,RMVar_hsa_circ_151690,RMVar_hsa_circ_151691,RMVar_hsa_circ_80913,RMVar_hsa_circ_303148,RMVar_hsa_circ_361122,RMVar_hsa_circ_288560,RMVar_hsa_circ_151696,RMVar_hsa_circ_151692,RMVar_hsa_circ_325769 21926 RMVar_ID_21926 Human_SNP_ID_472334366 A-to-I Human chr11 - 74131661 74131661 74131661 GAATTGCTTGAAACCTGGAGGCAGAGGTTGCAATGAGCCGAGAACATGCTACTGCACTCTGGCCT GAATTGCTTGAAACCTGGAGGCAGAGGTTGCAGTGAGCCGAGAACATGCTACTGCACTCTGGCCT T C C2CD3 Ensembl:ENSG00000168014 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs528251382 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6301,RMVar_hsa_circ_100073,RMVar_hsa_circ_113937,RMVar_hsa_circ_151665,RMVar_hsa_circ_78234,RMVar_hsa_circ_151664,RMVar_hsa_circ_92577,RMVar_hsa_circ_151666,RMVar_hsa_circ_151669,RMVar_hsa_circ_113843,RMVar_hsa_circ_151675,RMVar_hsa_circ_70342,RMVar_hsa_circ_97222,RMVar_hsa_circ_120544,RMVar_hsa_circ_94654,RMVar_hsa_circ_151681,RMVar_hsa_circ_151680,RMVar_hsa_circ_151683,RMVar_hsa_circ_104999,RMVar_hsa_circ_151684,RMVar_hsa_circ_85820,RMVar_hsa_circ_367622,RMVar_hsa_circ_151686,RMVar_hsa_circ_122885,RMVar_hsa_circ_151693,RMVar_hsa_circ_8871,RMVar_hsa_circ_151689,RMVar_hsa_circ_151690,RMVar_hsa_circ_151691,RMVar_hsa_circ_80913,RMVar_hsa_circ_303148,RMVar_hsa_circ_361122,RMVar_hsa_circ_288560,RMVar_hsa_circ_151696,RMVar_hsa_circ_151692,RMVar_hsa_circ_325769 21927 RMVar_ID_21927 Human_SNP_ID_472334481 A-to-I Human chr11 - 74132264 74132264 74132264 TCACTGCAACCTCCTCCTCCTGGGTTCAAGCAATTATCCTGCCTCTGCCTCCCAAGTAGCTGGTT TCACTGCAACCTCCTCCTCCTGGGTTCAAGCATTTATCCTGCCTCTGCCTCCCAAGTAGCTGGTT T A C2CD3 Ensembl:ENSG00000168014 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1565330494 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6301,RMVar_hsa_circ_100073,RMVar_hsa_circ_113937,RMVar_hsa_circ_151665,RMVar_hsa_circ_78234,RMVar_hsa_circ_151664,RMVar_hsa_circ_92577,RMVar_hsa_circ_151666,RMVar_hsa_circ_151669,RMVar_hsa_circ_113843,RMVar_hsa_circ_151675,RMVar_hsa_circ_70342,RMVar_hsa_circ_97222,RMVar_hsa_circ_120544,RMVar_hsa_circ_94654,RMVar_hsa_circ_151681,RMVar_hsa_circ_151680,RMVar_hsa_circ_151683,RMVar_hsa_circ_104999,RMVar_hsa_circ_151684,RMVar_hsa_circ_85820,RMVar_hsa_circ_367622,RMVar_hsa_circ_151686,RMVar_hsa_circ_122885,RMVar_hsa_circ_151693,RMVar_hsa_circ_8871,RMVar_hsa_circ_151689,RMVar_hsa_circ_151690,RMVar_hsa_circ_151691,RMVar_hsa_circ_80913,RMVar_hsa_circ_303148,RMVar_hsa_circ_361122,RMVar_hsa_circ_288560,RMVar_hsa_circ_151696,RMVar_hsa_circ_151692,RMVar_hsa_circ_325769 21928 RMVar_ID_21928 Human_SNP_ID_472334482 A-to-I Human chr11 - 74132265 74132265 74132265 CTCACTGCAACCTCCTCCTCCTGGGTTCAAGCAATTATCCTGCCTCTGCCTCCCAAGTAGCTGGT CTCACTGCAACCTCCTCCTCCTGGGTTCAAGCTATTATCCTGCCTCTGCCTCCCAAGTAGCTGGT T A C2CD3 Ensembl:ENSG00000168014 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1396932696 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6301,RMVar_hsa_circ_100073,RMVar_hsa_circ_113937,RMVar_hsa_circ_151665,RMVar_hsa_circ_78234,RMVar_hsa_circ_151664,RMVar_hsa_circ_92577,RMVar_hsa_circ_151666,RMVar_hsa_circ_151669,RMVar_hsa_circ_113843,RMVar_hsa_circ_151675,RMVar_hsa_circ_70342,RMVar_hsa_circ_97222,RMVar_hsa_circ_120544,RMVar_hsa_circ_94654,RMVar_hsa_circ_151681,RMVar_hsa_circ_151680,RMVar_hsa_circ_151683,RMVar_hsa_circ_104999,RMVar_hsa_circ_151684,RMVar_hsa_circ_85820,RMVar_hsa_circ_367622,RMVar_hsa_circ_151686,RMVar_hsa_circ_122885,RMVar_hsa_circ_151693,RMVar_hsa_circ_8871,RMVar_hsa_circ_151689,RMVar_hsa_circ_151690,RMVar_hsa_circ_151691,RMVar_hsa_circ_80913,RMVar_hsa_circ_303148,RMVar_hsa_circ_361122,RMVar_hsa_circ_288560,RMVar_hsa_circ_151696,RMVar_hsa_circ_151692,RMVar_hsa_circ_325769 21929 RMVar_ID_21929 Human_SNP_ID_472344655 A-to-I Human chr11 + 74175570 74175570 74175570 TTAAATTCCTTTTTTTTTCTTTTGCAAGAGATAGAGTCTTGCTGTGTTGCCCAGGCTGAAGTACA TTAAATTCCTTTTTTTTTCTTTTGCAAGAGATGGAGTCTTGCTGTGTTGCCCAGGCTGAAGTACA A G PPME1 Ensembl:ENSG00000214517 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1246562613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17560095 RMVar_hsa_circ_127618,RMVar_hsa_circ_151705,RMVar_hsa_circ_151704 21930 RMVar_ID_21930 Human_SNP_ID_472351632 A-to-I Human chr11 + 74206599 74206599 74206599 ATTTTATTTATGTATTTTTAAGACAGGATCTCAGTCTATCACCCAGATTAGTGTACAGTGGCACA ATTTTATTTATGTATTTTTAAGACAGGATCTCTGTCTATCACCCAGATTAGTGTACAGTGGCACA A T PPME1 Ensembl:ENSG00000214517 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1409344297 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11710995 RMVar_hsa_circ_3013,RMVar_hsa_circ_127618,RMVar_hsa_circ_151704,RMVar_hsa_circ_364842,RMVar_hsa_circ_65489,RMVar_hsa_circ_2123,RMVar_hsa_circ_151707,RMVar_hsa_circ_77964 21931 RMVar_ID_21931 Human_SNP_ID_472351635 A-to-I Human chr11 + 74206604 74206604 74206604 ATTTATGTATTTTTAAGACAGGATCTCAGTCTATCACCCAGATTAGTGTACAGTGGCACAATCAT ATTTATGTATTTTTAAGACAGGATCTCAGTCTGTCACCCAGATTAGTGTACAGTGGCACAATCAT A G PPME1 Ensembl:ENSG00000214517 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1304967096 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11710995 RMVar_hsa_circ_3013,RMVar_hsa_circ_127618,RMVar_hsa_circ_151704,RMVar_hsa_circ_364842,RMVar_hsa_circ_65489,RMVar_hsa_circ_2123,RMVar_hsa_circ_151707,RMVar_hsa_circ_77964 21932 RMVar_ID_21932 Human_SNP_ID_472352380 A-to-I Human chr11 + 74209939 74209939 74209939 ATACAGAAGTGGGGCATAGTGGCACATAACCTATAGTCTCAGTTACTTGGGGAGCTAAGGTGGGA ATACAGAAGTGGGGCATAGTGGCACATAACCTGTAGTCTCAGTTACTTGGGGAGCTAAGGTGGGA A G PPME1 Ensembl:ENSG00000214517 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs897690341 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3013,RMVar_hsa_circ_127618,RMVar_hsa_circ_151704,RMVar_hsa_circ_364842,RMVar_hsa_circ_65489,RMVar_hsa_circ_2123,RMVar_hsa_circ_151707,RMVar_hsa_circ_77964 21933 RMVar_ID_21933 Human_SNP_ID_472408448 A-to-I Human chr11 - 74455800 74455800 74455800 TTGTTTGAACCCGGGAGGTGGAGGTTGCAGTAAGCCAAGATCACGCCACTGCACTCCAGCCTGGG TTGTTTGAACCCGGGAGGTGGAGGTTGCAGTAGGCCAAGATCACGCCACTGCACTCCAGCCTGGG T C KCNE3 Ensembl:ENSG00000175538 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs897682076 Functional Loss SNV dbSNP153 33..33 33 - - - 21934 RMVar_ID_21934 Human_SNP_ID_472529915 A-to-I Human chr11 + 74966817 74966817 74966817 ACAGGGTCTTACCGTGTCACCCAGGCTGAAGTACAGTGGTGTGATCATGACTCACTGCAGCGTCA ACAGGGTCTTACCGTGTCACCCAGGCTGAAGTTCAGTGGTGTGATCATGACTCACTGCAGCGTCA A T SPCS2 Ensembl:ENSG00000118363 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1352588810 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17560098 RMVar_hsa_circ_19257,RMVar_hsa_circ_284827 21935 RMVar_ID_21935 Human_SNP_ID_472530069 A-to-I Human chr11 + 74967530 74967530 74967530 CCAACACTTTGAGAGGCCAAGGCGGGCGAATCACTTGAGCCCAAGAGTTCAAGGCCAGCCTGAGC CCAACACTTTGAGAGGCCAAGGCGGGCGAATCGCTTGAGCCCAAGAGTTCAAGGCCAGCCTGAGC A G SPCS2 Ensembl:ENSG00000118363 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs496698 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19257,RMVar_hsa_circ_284827 21936 RMVar_ID_21936 Human_SNP_ID_472530070 A-to-I Human chr11 + 74967530 74967530 74967530 CCAACACTTTGAGAGGCCAAGGCGGGCGAATCACTTGAGCCCAAGAGTTCAAGGCCAGCCTGAGC CCAACACTTTGAGAGGCCAAGGCGGGCGAATCTCTTGAGCCCAAGAGTTCAAGGCCAGCCTGAGC A T SPCS2 Ensembl:ENSG00000118363 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs496698 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19257,RMVar_hsa_circ_284827 21937 RMVar_ID_21937 Human_SNP_ID_472533283 A-to-I Human chr11 + 74982376 74982376 74982376 TAAACCTGCTCATTTCAAGGTAGCTTACTGCCAACAGAACACTGAGGTACAGCCCAAGAAGAATG TAAACCTGCTCATTTCAAGGTAGCTTACTGCCGACAGAACACTGAGGTACAGCCCAAGAAGAATG A G lnc-SPCS2-1 RNACentral:URS00008BCC77 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917182446 Functional Loss SNV dbSNP153 33..33 33 - - - 21938 RMVar_ID_21938 Human_SNP_ID_472577525 A-to-I Human chr11 + 75172674 75172674 75172674 CACTTCGGCTGGGCGTGGTGGCTCACATCTGTAGTTCCAGCACTTTGGGAGGCCAAGGCGGTTGG CACTTCGGCTGGGCGTGGTGGCTCACATCTGTGGTTCCAGCACTTTGGGAGGCCAAGGCGGTTGG A G SLCO2B1 Ensembl:ENSG00000137491 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1362343874 Functional Loss SNV dbSNP153 33..33 33 - - - 21939 RMVar_ID_21939 Human_SNP_ID_472616274 A-to-I Human chr11 - 75329763 75329763 75329763 GTCTCAAACTCTTGGGCTCAAGCAATCCTCCCACCTTGATCTCCCAAAGCACTGGGATTACAGGC GTCTCAAACTCTTGGGCTCAAGCAATCCTCCCGCCTTGATCTCCCAAAGCACTGGGATTACAGGC T C ARRB1 Ensembl:ENSG00000137486 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1284394063 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17560100 21940 RMVar_ID_21940 Human_SNP_ID_472617275 A-to-I Human chr11 + 75334085 75334085 75334085 CGGGCGCGGTGGCTCACGCTTGTAATCCCAGCACTTTGGGAGGCCCAGGTGGGCAGACCACAAGG CGGGCGCGGTGGCTCACGCTTGTAATCCCAGCGCTTTGGGAGGCCCAGGTGGGCAGACCACAAGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs940988202 Functional Loss SNV dbSNP153 33..33 33 - - - 21941 RMVar_ID_21941 Human_SNP_ID_472676374 A-to-I Human chr11 + 75567425 75567425 75567425 CTCACTGCAGCCTTGGCCTCCGGGCTTCAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGG CTCACTGCAGCCTTGGCCTCCGGGCTTCAAGCTATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGG A T SERPINH1 Ensembl:ENSG00000149257 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1359493686 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23681,RMVar_hsa_circ_119542,RMVar_hsa_circ_151805 21942 RMVar_ID_21942 Human_SNP_ID_472676400 A-to-I Human chr11 + 75567556 75567556 75567556 GTTGGCCAGGCTGGTCTCAAACTTTTGGTCTCAAGTGATCTGCCCGCCTCGGCCTCCCAAAGTGC GTTGGCCAGGCTGGTCTCAAACTTTTGGTCTCGAGTGATCTGCCCGCCTCGGCCTCCCAAAGTGC A G SERPINH1 Ensembl:ENSG00000149257 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs927516813 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23681,RMVar_hsa_circ_119542,RMVar_hsa_circ_151805 21943 RMVar_ID_21943 Human_SNP_ID_472685200 A-to-I Human chr11 - 75603926 75603926 75603926 CATGATCTTAATTGTATCCAGAGGATTTGCCAATGTATGTTCAGTCTCTCAAGATTTGGCATTAG CATGATCTTAATTGTATCCAGAGGATTTGCCAGTGTATGTTCAGTCTCTCAAGATTTGGCATTAG T C MAP6 Ensembl:ENSG00000171533 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs540937127 Functional Loss SNV dbSNP153 33..33 33 - - - 21944 RMVar_ID_21944 Human_SNP_ID_472735783 A-to-I Human chr11 + 75820192 75820192 75820192 TAGAGATGGGGTCTTGCTGTGTTGCCCAGGCTAGTCTCAAACTCCTGGCCTCAAGATATCCTCCC TAGAGATGGGGTCTTGCTGTGTTGCCCAGGCTGGTCTCAAACTCCTGGCCTCAAGATATCCTCCC A G UVRAG Ensembl:ENSG00000198382 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1416498415 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8359123 21945 RMVar_ID_21945 Human_SNP_ID_472758903 A-to-I Human chr11 + 75915123 75915123 75915123 AAAATTAACCAGGCATGGTGACACATGCCTGTAGTCCCAGCTGCTCGGGAGGCTGAGGCAGGAGA AAAATTAACCAGGCATGGTGACACATGCCTGTGGTCCCAGCTGCTCGGGAGGCTGAGGCAGGAGA A G UVRAG,AP003168.2 Ensembl:ENSG00000198382,Ensembl:ENSG00000255081 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1445668546 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_362102,RMVar_hsa_circ_358357,RMVar_hsa_circ_72476,RMVar_hsa_circ_17718,RMVar_hsa_circ_29678,RMVar_hsa_circ_51876,RMVar_hsa_circ_357644,RMVar_hsa_circ_48033,RMVar_hsa_circ_842,RMVar_hsa_circ_151820,RMVar_hsa_circ_318123,RMVar_hsa_circ_370783,RMVar_hsa_circ_50140 21946 RMVar_ID_21946 Human_SNP_ID_472787971 A-to-I Human chr11 + 76040815 76040815 76040815 CTGACTTTGTGATCCGCCTGCCTTGGCCTCCCAAGGTGCTGGGATTACAGGTGTGAGCCACCGGG CTGACTTTGTGATCCGCCTGCCTTGGCCTCCCGAGGTGCTGGGATTACAGGTGTGAGCCACCGGG A G UVRAG Ensembl:ENSG00000198382 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1425675282 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32211,RMVar_hsa_circ_29678,RMVar_hsa_circ_55686,RMVar_hsa_circ_59685,RMVar_hsa_circ_340191 21947 RMVar_ID_21947 Human_SNP_ID_472807890 A-to-I Human chr11 + 76127688 76127688 76127688 TGAATGAATGAATCAATGAGGCCTGGCGTGGTAGCTCACACCTGTAATCCCAGCACTTTAGGAGG TGAATGAATGAATCAATGAGGCCTGGCGTGGTGGCTCACACCTGTAATCCCAGCACTTTAGGAGG A G UVRAG Ensembl:ENSG00000198382 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1413088367 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11718597,Human_RBP_ID_18613069 21948 RMVar_ID_21948 Human_SNP_ID_472865867 A-to-I Human chr11 - 76353804 76353804 76353804 GGGTTTCACCATATTGGCCAGGCTGGTCTCAAACTCCTGACCTCGTGATCCACCCACCTCAGCCT GGGTTTCACCATATTGGCCAGGCTGGTCTCAATCTCCTGACCTCGTGATCCACCCACCTCAGCCT T A THAP12 Ensembl:ENSG00000137492 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs931139064 Functional Loss SNV dbSNP153 33..33 33 - - - 21949 RMVar_ID_21949 Human_SNP_ID_472873785 A-to-I Human chr11 + 76384583 76384583 76384583 GACCTCAGGTGATCCACCCACCTCGGCGTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCACG GACCTCAGGTGATCCACCCACCTCGGCGTCCCGAAGTGCTGGGATTACAGGCGTGAGCCACCACG A G GVQW3 Ensembl:ENSG00000179240 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs545779840 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24903204 21950 RMVar_ID_21950 Human_SNP_ID_472908977 A-to-I Human chr11 + 76538359 76538359 76538359 ATGATTCACTGCAGCCTCAACTTCCTGGGCTCAGGTGATCCTCCTGCCTCAGCCTCCTGAGTAGC ATGATTCACTGCAGCCTCAACTTCCTGGGCTCGGGTGATCCTCCTGCCTCAGCCTCCTGAGTAGC A G EMSY Ensembl:ENSG00000158636 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs969850913 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5928,RMVar_hsa_circ_100418,RMVar_hsa_circ_151837,RMVar_hsa_circ_115760,RMVar_hsa_circ_36721,RMVar_hsa_circ_151848,RMVar_hsa_circ_57819,RMVar_hsa_circ_17194,RMVar_hsa_circ_151858,RMVar_hsa_circ_105611 21951 RMVar_ID_21951 Human_SNP_ID_472908981 A-to-I Human chr11 + 76538389 76538389 76538389 TCAGGTGATCCTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGTGTGTGCCACTATGCCTG TCAGGTGATCCTCCTGCCTCAGCCTCCTGAGTGGCTGGGACTACAGGTGTGTGCCACTATGCCTG A G EMSY Ensembl:ENSG00000158636 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs374029412 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5928,RMVar_hsa_circ_100418,RMVar_hsa_circ_151837,RMVar_hsa_circ_115760,RMVar_hsa_circ_36721,RMVar_hsa_circ_151848,RMVar_hsa_circ_57819,RMVar_hsa_circ_17194,RMVar_hsa_circ_151858,RMVar_hsa_circ_105611 21952 RMVar_ID_21952 Human_SNP_ID_472976546 A-to-I Human chr11 + 76802443 76802443 76802443 GTCTTGAACTCCTGAGCTCAAGAAATCCTCCCACCTCAGCCTCCCAAAGCGTTGAGATTACATGT GTCTTGAACTCCTGAGCTCAAGAAATCCTCCCCCCTCAGCCTCCCAAAGCGTTGAGATTACATGT A C AP003119.3 Ensembl:ENSG00000261578 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs922570214 Functional Loss SNV dbSNP153 33..33 33 - - - 21953 RMVar_ID_21953 Human_SNP_ID_473028550 A-to-I Human chr11 + 77023856 77023856 77023856 AGCACTTTGGGAGGCCGAGGTGAGCAGATCACAAGGTCAGGAGATCGAGACCATCCTGGCTAACA AGCACTTTGGGAGGCCGAGGTGAGCAGATCACGAGGTCAGGAGATCGAGACCATCCTGGCTAACA A G ACER3 Ensembl:ENSG00000078124 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1555025024 Functional Loss SNV dbSNP153 33..33 33 - - - 21954 RMVar_ID_21954 Human_SNP_ID_473029103 A-to-I Human chr11 + 77025680 77025680 77025680 CACCTGCCTTGGCCTCCCAAAGTCCTGGAATTACAGGCGTGAGCTACCGTGCCCAGCTGGTTTTT CACCTGCCTTGGCCTCCCAAAGTCCTGGAATTCCAGGCGTGAGCTACCGTGCCCAGCTGGTTTTT A C ACER3 Ensembl:ENSG00000078124 Protein coding 3'UTR GSE38233;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29796672,31158229,31158229,32596459 RNA-Seq:(High) rs1304291806 Functional Loss SNV dbSNP153 33..33 33 - - - 21955 RMVar_ID_21955 Human_SNP_ID_473120876 A-to-I Human chr11 - 77378690 77378690 77378690 CCAGCTACTTGGGAAGCTGAGGAGAAGGGATCACTTGAGCCTGGGAGGTGGAGTTGCAGTGAGCA CCAGCTACTTGGGAAGCTGAGGAGAAGGGATCTCTTGAGCCTGGGAGGTGGAGTTGCAGTGAGCA T A PAK1 Ensembl:ENSG00000149269 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1169821825 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24903662 RMVar_hsa_circ_296024,RMVar_hsa_circ_319744,RMVar_hsa_circ_26103,RMVar_hsa_circ_151880,RMVar_hsa_circ_151881,RMVar_hsa_circ_96052,RMVar_hsa_circ_151889,RMVar_hsa_circ_151887,RMVar_hsa_circ_116738,RMVar_hsa_circ_363548,RMVar_hsa_circ_274840,RMVar_hsa_circ_18022,RMVar_hsa_circ_151896,RMVar_hsa_circ_4653,RMVar_hsa_circ_151891,RMVar_hsa_circ_331982,RMVar_hsa_circ_344888,RMVar_hsa_circ_280860,RMVar_hsa_circ_151892,RMVar_hsa_circ_293549,RMVar_hsa_circ_151894,RMVar_hsa_circ_337928,RMVar_hsa_circ_62267,RMVar_hsa_circ_282842,RMVar_hsa_circ_151897,RMVar_hsa_circ_151902,RMVar_hsa_circ_282238,RMVar_hsa_circ_295669,RMVar_hsa_circ_115431,RMVar_hsa_circ_151903,RMVar_hsa_circ_151905,RMVar_hsa_circ_151900,RMVar_hsa_circ_151901,RMVar_hsa_circ_286723,RMVar_hsa_circ_279830,RMVar_hsa_circ_151904 21956 RMVar_ID_21956 Human_SNP_ID_473156045 A-to-I Human chr11 - 77527200 77527200 77527200 TACTCAGGAGGCTGAGATGGGAGGATTCCTTGAGCCTGGGAGGCGGAGGTTGCAGTGAGCCGAGA TACTCAGGAGGCTGAGATGGGAGGATTCCTTGGGCCTGGGAGGCGGAGGTTGCAGTGAGCCGAGA T C CLNS1A Ensembl:ENSG00000074201 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1324073981 Functional Loss SNV dbSNP153 33..33 33 - - - 21957 RMVar_ID_21957 Human_SNP_ID_473173615 A-to-I Human chr11 - 77600768 77600768 77600768 GACCTCGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCACC GACCTCGTGATCCGCCCGCCTCGGCCTCCCAAGGTGCTGGGATTACAGGCGTGAGCCACCGCACC T C CLNS1A Ensembl:ENSG00000074201 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs547375371 Functional Loss SNV dbSNP153 33..33 33 - - - 21958 RMVar_ID_21958 Human_SNP_ID_473176594 A-to-I Human chr11 - 77614221 77614221 77614221 AATTAGCTGGGCGTGGTGGTGGGGCACCTCTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAC AATTAGCTGGGCGTGGTGGTGGGGCACCTCTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAC T C CLNS1A Ensembl:ENSG00000074201 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs745462915 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_151908 21959 RMVar_ID_21959 Human_SNP_ID_473177203 A-to-I Human chr11 - 77617111 77617111 77617111 CGCCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCACACCTGGCTGTGTAAA CGCCTGCCTTGGCCTCCCAAAGTGCTGGGATTGCAGGTGTGAGCCACCACACCTGGCTGTGTAAA T C CLNS1A Ensembl:ENSG00000074201 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1407777388 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_151910,RMVar_hsa_circ_107270,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_151913,RMVar_hsa_circ_151911,RMVar_hsa_circ_151909 21960 RMVar_ID_21960 Human_SNP_ID_473177768 A-to-I Human chr11 - 77619510 77619510 77619510 CTTTTTAAAATTCTTTCTTGAGACAGGGTCTTACTCTGTCACCCAGGCTAGAGTGCAGTGGCATG CTTTTTAAAATTCTTTCTTGAGACAGGGTCTTGCTCTGTCACCCAGGCTAGAGTGCAGTGGCATG T C CLNS1A Ensembl:ENSG00000074201 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs983363594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19680959,Human_RBP_ID_26897716 RMVar_hsa_circ_151910,RMVar_hsa_circ_107270,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_151913,RMVar_hsa_circ_151911,RMVar_hsa_circ_151909 21961 RMVar_ID_21961 Human_SNP_ID_473179528 A-to-I Human chr11 - 77626248 77626246 77626248 TAAGACCCCATCTCAAAAAAACAAAAATTAGCAGGGTGTGGTGGCAAGTGCCTGTAGTCCCAGCT TAAGACCCCATCTCAAAAAAACAAAAATTAGC__GGTGTGGTGGCAAGTGCCTGTAGTCCCAGCT CCT C CLNS1A Ensembl:ENSG00000074201 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs951326990 Functional Loss DEL dbSNP153 33..34 33 - - - 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_151923,RMVar_hsa_circ_151922 21962 RMVar_ID_21962 Human_SNP_ID_473179531 A-to-I Human chr11 - 77626251 77626251 77626251 TCGTAAGACCCCATCTCAAAAAAACAAAAATTAGCAGGGTGTGGTGGCAAGTGCCTGTAGTCCCA TCGTAAGACCCCATCTCAAAAAAACAAAAATTTGCAGGGTGTGGTGGCAAGTGCCTGTAGTCCCA T A CLNS1A Ensembl:ENSG00000074201 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs555876627 Functional Loss SNV dbSNP153 33..33 33 - - - 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_151923,RMVar_hsa_circ_151922 21963 RMVar_ID_21963 Human_SNP_ID_473179540 A-to-I Human chr11 - 77626279 77626279 77626279 CAGGAGTTTCAGACCAGCCTGGGCAACATCGTAAGACCCCATCTCAAAAAAACAAAAATTAGCAG CAGGAGTTTCAGACCAGCCTGGGCAACATCGTGAGACCCCATCTCAAAAAAACAAAAATTAGCAG T C CLNS1A Ensembl:ENSG00000074201 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs976601363 Functional Loss SNV dbSNP153 33..33 33 - - - 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_151923,RMVar_hsa_circ_151922 21964 RMVar_ID_21964 Human_SNP_ID_473181208 A-to-I Human chr11 - 77632871 77632871 77632871 TGTTGGTAGTCTGGTCTGGAACTCCTGACCTCAGGTGATCCATCCACCTCGGCCTCCCAAAATGC TGTTGGTAGTCTGGTCTGGAACTCCTGACCTCGGGTGATCCATCCACCTCGGCCTCCCAAAATGC T C CLNS1A Ensembl:ENSG00000074201 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs928381531 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94520,RMVar_hsa_circ_85782,RMVar_hsa_circ_151909,RMVar_hsa_circ_94585,RMVar_hsa_circ_151919,RMVar_hsa_circ_151922 21965 RMVar_ID_21965 Human_SNP_ID_473181242 A-to-I Human chr11 - 77633004 77633004 77633004 TGGTTCACTGCAACCTCCGCCTCCTGGATTCAACCAATTCTCCTGCCTCAGCCTCCCAAGTAGCT TGGTTCACTGCAACCTCCGCCTCCTGGATTCACCCAATTCTCCTGCCTCAGCCTCCCAAGTAGCT T G CLNS1A Ensembl:ENSG00000074201 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1433816296 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94520,RMVar_hsa_circ_85782,RMVar_hsa_circ_151909,RMVar_hsa_circ_94585,RMVar_hsa_circ_151919,RMVar_hsa_circ_151922 21966 RMVar_ID_21966 Human_SNP_ID_473181820 A-to-I Human chr11 - 77635425 77635425 77635425 ATCGCTTGAACCCGAGAGGCGGAGGTTGTAGTAAGCCGAGATCATGCCATTGCATTCCAGCCTGG ATCGCTTGAACCCGAGAGGCGGAGGTTGTAGTGAGCCGAGATCATGCCATTGCATTCCAGCCTGG T C CLNS1A Ensembl:ENSG00000074201 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1285455028 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94520,RMVar_hsa_circ_85782,RMVar_hsa_circ_151909,RMVar_hsa_circ_94585,RMVar_hsa_circ_151919,RMVar_hsa_circ_151922 21967 RMVar_ID_21967 Human_SNP_ID_473202193 A-to-I Human chr11 - 77715088 77715088 77715088 ATAAGGTCTTGCTCAATTGCCCAGGATAGAATACAGTGTCATGATCATAAATCACTGTAACCTTG ATAAGGTCTTGCTCAATTGCCCAGGATAGAATGCAGTGTCATGATCATAAATCACTGTAACCTTG T C RSF1 Ensembl:ENSG00000048649 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1389571539 Functional Loss SNV dbSNP153 33..33 33 - - - 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_151953,RMVar_hsa_circ_46579 21968 RMVar_ID_21968 Human_SNP_ID_473214061 A-to-I Human chr11 - 77763154 77763154 77763154 TTGTATTATTAGTAGAGACAGGGTTTCACCATATTGGCCAGGCTAGTCTCGAACTCCTGACCTCG TTGTATTATTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTAGTCTCGAACTCCTGACCTCG T C RSF1 Ensembl:ENSG00000048649 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1422010667 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269184,RMVar_hsa_circ_268557,RMVar_hsa_circ_46579,RMVar_hsa_circ_151961,RMVar_hsa_circ_273483,RMVar_hsa_circ_273441,RMVar_hsa_circ_151965 21969 RMVar_ID_21969 Human_SNP_ID_473214062 A-to-I Human chr11 - 77763159 77763159 77763159 TTTTTTTGTATTATTAGTAGAGACAGGGTTTCACCATATTGGCCAGGCTAGTCTCGAACTCCTGA TTTTTTTGTATTATTAGTAGAGACAGGGTTTCGCCATATTGGCCAGGCTAGTCTCGAACTCCTGA T C RSF1 Ensembl:ENSG00000048649 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs941291297 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269184,RMVar_hsa_circ_268557,RMVar_hsa_circ_46579,RMVar_hsa_circ_151961,RMVar_hsa_circ_273483,RMVar_hsa_circ_273441,RMVar_hsa_circ_151965 21970 RMVar_ID_21970 Human_SNP_ID_473226057 A-to-I Human chr11 - 77810705 77810705 77810705 AAAATACAAATTAGTTGGATGTGGTGGGATACACCTGTAATCCCAGCTACCTAGGAGGCTGCCAC AAAATACAAATTAGTTGGATGTGGTGGGATACGCCTGTAATCCCAGCTACCTAGGAGGCTGCCAC T C RSF1 Ensembl:ENSG00000048649 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1053586391 Functional Loss SNV dbSNP153 33..33 33 - - - 21971 RMVar_ID_21971 Human_SNP_ID_473229917 A-to-I Human chr11 + 77825017 77825017 77825017 TTGTTTTTCTTTTTGAGACAGAGTCTCACTCTATCACCCAGGCTAGAGTGCAGTGACGCGATCTC TTGTTTTTCTTTTTGAGACAGAGTCTCACTCTGTCACCCAGGCTAGAGTGCAGTGACGCGATCTC A G AAMDC Ensembl:ENSG00000087884 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1325657065 Functional Loss SNV dbSNP153 33..33 33 - - - 21972 RMVar_ID_21972 Human_SNP_ID_473232895 A-to-I Human chr11 + 77837799 77837799 77837799 GAAATTGAGCCTGGGCACAGTGGCTCATGCCTATAATGCAAGCACTTGGGAGGCTGAGAAGACAG GAAATTGAGCCTGGGCACAGTGGCTCATGCCTCTAATGCAAGCACTTGGGAGGCTGAGAAGACAG A C AAMDC Ensembl:ENSG00000087884 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928482293 Functional Loss SNV dbSNP153 33..33 33 - - - 21973 RMVar_ID_21973 Human_SNP_ID_473232896 A-to-I Human chr11 + 77837799 77837799 77837799 GAAATTGAGCCTGGGCACAGTGGCTCATGCCTATAATGCAAGCACTTGGGAGGCTGAGAAGACAG GAAATTGAGCCTGGGCACAGTGGCTCATGCCTGTAATGCAAGCACTTGGGAGGCTGAGAAGACAG A G AAMDC Ensembl:ENSG00000087884 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928482293 Functional Loss SNV dbSNP153 33..33 33 - - - 21974 RMVar_ID_21974 Human_SNP_ID_473236923 A-to-I Human chr11 - 77856066 77856066 77856066 TCACCCAGGCTGGAGTGCAATGGGGCAATCTCAGCTCACTGCAACTCTGCCTCCTGGGCTCAAGG TCACCCAGGCTGGAGTGCAATGGGGCAATCTCGGCTCACTGCAACTCTGCCTCCTGGGCTCAAGG T C AP002812.2 Ensembl:ENSG00000254459 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs578051787 Functional Loss SNV dbSNP153 33..33 33 - - - 21975 RMVar_ID_21975 Human_SNP_ID_473243041 A-to-I Human chr11 - 77882142 77882141 77882143 GGAGGCTGAGGTGGGAGGATCGATTGAGCCCAAGAGTCTGAGACCAGCATGGGCAATATAGGGCA GGAGGCTGAGGTGGGAGGATCGATTGAGCCC__GAGTCTGAGACCAGCATGGGCAATATAGGGCA CTT C INTS4 Ensembl:ENSG00000149262 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs767317608 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_105391,RMVar_hsa_circ_151970 21976 RMVar_ID_21976 Human_SNP_ID_473243042 A-to-I Human chr11 - 77882142 77882142 77882142 GGAGGCTGAGGTGGGAGGATCGATTGAGCCCAAGAGTCTGAGACCAGCATGGGCAATATAGGGCA GGAGGCTGAGGTGGGAGGATCGATTGAGCCCAGGAGTCTGAGACCAGCATGGGCAATATAGGGCA T C INTS4 Ensembl:ENSG00000149262 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025201711 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105391,RMVar_hsa_circ_151970 21977 RMVar_ID_21977 Human_SNP_ID_473243043 A-to-I Human chr11 - 77882142 77882142 77882142 GGAGGCTGAGGTGGGAGGATCGATTGAGCCCAAGAGTCTGAGACCAGCATGGGCAATATAGGGCA GGAGGCTGAGGTGGGAGGATCGATTGAGCCCACGAGTCTGAGACCAGCATGGGCAATATAGGGCA T G INTS4 Ensembl:ENSG00000149262 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025201711 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105391,RMVar_hsa_circ_151970 21978 RMVar_ID_21978 Human_SNP_ID_473252506 A-to-I Human chr11 - 77923155 77923155 77923155 TGCCACCATGCCCAGCTAATTTTTGTATTTTTAGCAGAGATGGGGTTTCACCATGTTGGCCAGGA TGCCACCATGCCCAGCTAATTTTTGTATTTTTGGCAGAGATGGGGTTTCACCATGTTGGCCAGGA T C INTS4 Ensembl:ENSG00000149262 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs1343271982 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100632,RMVar_hsa_circ_105391,RMVar_hsa_circ_112096,RMVar_hsa_circ_151970,RMVar_hsa_circ_109865,RMVar_hsa_circ_151973,RMVar_hsa_circ_151974,RMVar_hsa_circ_110271,RMVar_hsa_circ_77896,RMVar_hsa_circ_151976,RMVar_hsa_circ_151977,RMVar_hsa_circ_151975,RMVar_hsa_circ_290055,RMVar_hsa_circ_42601,RMVar_hsa_circ_17195,RMVar_hsa_circ_59063,RMVar_hsa_circ_362508,RMVar_hsa_circ_355602,RMVar_hsa_circ_117058,RMVar_hsa_circ_151984,RMVar_hsa_circ_151985,RMVar_hsa_circ_46091,RMVar_hsa_circ_357177,RMVar_hsa_circ_21227,RMVar_hsa_circ_151987,RMVar_hsa_circ_363038,RMVar_hsa_circ_372219,RMVar_hsa_circ_36132,RMVar_hsa_circ_102040,RMVar_hsa_circ_376071,RMVar_hsa_circ_26488,RMVar_hsa_circ_151989,RMVar_hsa_circ_151988 21979 RMVar_ID_21979 Human_SNP_ID_473252790 A-to-I Human chr11 - 77924279 77924279 77924279 CTCCTGCCTCAGCCTCTCGAGTAACTGGGATTATAGGTTGCATGCCACCATACCCCAACTAATTT CTCCTGCCTCAGCCTCTCGAGTAACTGGGATTGTAGGTTGCATGCCACCATACCCCAACTAATTT T C INTS4 Ensembl:ENSG00000149262 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs994421756 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100632,RMVar_hsa_circ_105391,RMVar_hsa_circ_112096,RMVar_hsa_circ_151970,RMVar_hsa_circ_109865,RMVar_hsa_circ_151973,RMVar_hsa_circ_151974,RMVar_hsa_circ_110271,RMVar_hsa_circ_77896,RMVar_hsa_circ_151976,RMVar_hsa_circ_151977,RMVar_hsa_circ_151975,RMVar_hsa_circ_290055,RMVar_hsa_circ_42601,RMVar_hsa_circ_17195,RMVar_hsa_circ_59063,RMVar_hsa_circ_362508,RMVar_hsa_circ_355602,RMVar_hsa_circ_117058,RMVar_hsa_circ_151984,RMVar_hsa_circ_151985,RMVar_hsa_circ_46091,RMVar_hsa_circ_357177,RMVar_hsa_circ_21227,RMVar_hsa_circ_151987,RMVar_hsa_circ_363038,RMVar_hsa_circ_372219,RMVar_hsa_circ_36132,RMVar_hsa_circ_102040,RMVar_hsa_circ_376071,RMVar_hsa_circ_26488,RMVar_hsa_circ_151989,RMVar_hsa_circ_151988 21980 RMVar_ID_21980 Human_SNP_ID_473267625 A-to-I Human chr11 + 77985249 77985248 77985249 CATACTTCCCCTCAGAGTGACATTTCTAAAACAAAAACTGACAAGGTAGAATACAAGGCCCTTTA CATACTTCCCCTCAGAGTGACATTTCTAAAAC_AAAACTGACAAGGTAGAATACAAGGCCCTTTA CA C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1385137164 Functional Loss DEL dbSNP153 33..33 33 - - - 21981 RMVar_ID_21981 Human_SNP_ID_473268055 A-to-I Human chr11 - 77987193 77987188 77987193 ATATATACTATGTAAGTAAAGAGAATAGTTTAATTAATTCCCATGTACCCATTACCTGGCTTCAA ATATATACTATGTAAGTAAAGAGAATAGTTTA_____TTCCCATGTACCCATTACCTGGCTTCAA ATTAAT A INTS4 Ensembl:ENSG00000149262 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs890398322 Functional Loss DEL dbSNP153 33..37 33 - - - RMVar_hsa_circ_42601,RMVar_hsa_circ_117058,RMVar_hsa_circ_151985,RMVar_hsa_circ_376071,RMVar_hsa_circ_151988,RMVar_hsa_circ_368447,RMVar_hsa_circ_276488,RMVar_hsa_circ_152003,RMVar_hsa_circ_20185,RMVar_hsa_circ_152007,RMVar_hsa_circ_338330 21982 RMVar_ID_21982 Human_SNP_ID_473268087 A-to-I Human chr11 - 77987308 77987308 77987308 ATGGAACTAAGCTTAGAGCTGTTTAGTATCCAAGGTCACCCAGCTAGTAAATGGAAGGTATGGAT ATGGAACTAAGCTTAGAGCTGTTTAGTATCCAGGGTCACCCAGCTAGTAAATGGAAGGTATGGAT T C INTS4 Ensembl:ENSG00000149262 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1358215280 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42601,RMVar_hsa_circ_117058,RMVar_hsa_circ_151985,RMVar_hsa_circ_376071,RMVar_hsa_circ_151988,RMVar_hsa_circ_368447,RMVar_hsa_circ_276488,RMVar_hsa_circ_152003,RMVar_hsa_circ_20185,RMVar_hsa_circ_152007,RMVar_hsa_circ_338330 21983 RMVar_ID_21983 Human_SNP_ID_473268089 A-to-I Human chr11 - 77987313 77987313 77987313 CAGATATGGAACTAAGCTTAGAGCTGTTTAGTATCCAAGGTCACCCAGCTAGTAAATGGAAGGTA CAGATATGGAACTAAGCTTAGAGCTGTTTAGTGTCCAAGGTCACCCAGCTAGTAAATGGAAGGTA T C INTS4 Ensembl:ENSG00000149262 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1213954943 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42601,RMVar_hsa_circ_117058,RMVar_hsa_circ_151985,RMVar_hsa_circ_376071,RMVar_hsa_circ_151988,RMVar_hsa_circ_368447,RMVar_hsa_circ_276488,RMVar_hsa_circ_152003,RMVar_hsa_circ_20185,RMVar_hsa_circ_152007,RMVar_hsa_circ_338330 21984 RMVar_ID_21984 Human_SNP_ID_473268092 A-to-I Human chr11 - 77987331 77987331 77987331 ATTGTTATCTCTAAATTCCAGATATGGAACTAAGCTTAGAGCTGTTTAGTATCCAAGGTCACCCA ATTGTTATCTCTAAATTCCAGATATGGAACTAGGCTTAGAGCTGTTTAGTATCCAAGGTCACCCA T C INTS4 Ensembl:ENSG00000149262 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs898508869 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42601,RMVar_hsa_circ_117058,RMVar_hsa_circ_151985,RMVar_hsa_circ_376071,RMVar_hsa_circ_151988,RMVar_hsa_circ_368447,RMVar_hsa_circ_276488,RMVar_hsa_circ_152003,RMVar_hsa_circ_20185,RMVar_hsa_circ_152007,RMVar_hsa_circ_338330 21985 RMVar_ID_21985 Human_SNP_ID_473289140 A-to-I Human chr11 - 78068542 78068542 78068542 GACCTTGTGATCCACCTGCCTTGGCCTTCCAAAGTGTTGGAATTACAGGCGTGAGCCACCGCGCC GACCTTGTGATCCACCTGCCTTGGCCTTCCAAGGTGTTGGAATTACAGGCGTGAGCCACCGCGCC T C NDUFC2-KCTD14,NDUFC2 Ensembl:ENSG00000259112,Ensembl:ENSG00000151366 Protein coding,Protein coding intron,3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1332836396 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26409880 RMVar_hsa_circ_95576,RMVar_hsa_circ_152009 21986 RMVar_ID_21986 Human_SNP_ID_473289156 A-to-I Human chr11 - 78068602 78068602 78068602 TTTTGTGTTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAAGATGGTCTCAATCTCTTGACCT TTTTGTGTTTTTAGTAGAGACGGGGTTTCACCGTGTTGGCCAAGATGGTCTCAATCTCTTGACCT T C NDUFC2-KCTD14,NDUFC2 Ensembl:ENSG00000259112,Ensembl:ENSG00000151366 Protein coding,Protein coding intron,3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs987977754 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95576,RMVar_hsa_circ_152009 21987 RMVar_ID_21987 Human_SNP_ID_473289176 A-to-I Human chr11 - 78068661 78068661 78068661 CCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGTGCATGCCACGACGCCCAGCTGATTTTTGT CCTGCCTCAGCCTCCCGAGTAGCTGGGACTACGGGTGCATGCCACGACGCCCAGCTGATTTTTGT T C NDUFC2-KCTD14,NDUFC2 Ensembl:ENSG00000259112,Ensembl:ENSG00000151366 Protein coding,Protein coding intron,3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1014172314 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95576,RMVar_hsa_circ_152009 21988 RMVar_ID_21988 Human_SNP_ID_473289307 A-to-I Human chr11 - 78069027 78069027 78069027 AAAATTAGCTGGGCGTGGTGGCACGTTCCTGCAATCCCAGCTACTCATAAGGCTGAGGTGGGAGG AAAATTAGCTGGGCGTGGTGGCACGTTCCTGCGATCCCAGCTACTCATAAGGCTGAGGTGGGAGG T C NDUFC2-KCTD14,NDUFC2 Ensembl:ENSG00000259112,Ensembl:ENSG00000151366 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1166220685 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_404339,Human_RBP_ID_8175284,Human_RBP_ID_26407340 RMVar_hsa_circ_95576,RMVar_hsa_circ_152009 21989 RMVar_ID_21989 Human_SNP_ID_473289317 A-to-I Human chr11 - 78069056 78069056 78069056 GGTGAAACACTGTCTCTACATAAAATACAAAAATTAGCTGGGCGTGGTGGCACGTTCCTGCAATC GGTGAAACACTGTCTCTACATAAAATACAAAAGTTAGCTGGGCGTGGTGGCACGTTCCTGCAATC T C NDUFC2-KCTD14,NDUFC2 Ensembl:ENSG00000259112,Ensembl:ENSG00000151366 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1291496680 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95576,RMVar_hsa_circ_152009 21990 RMVar_ID_21990 Human_SNP_ID_473289320 A-to-I Human chr11 - 78069069 78069069 78069069 ACTTGGGCAACATGGTGAAACACTGTCTCTACATAAAATACAAAAATTAGCTGGGCGTGGTGGCA ACTTGGGCAACATGGTGAAACACTGTCTCTACGTAAAATACAAAAATTAGCTGGGCGTGGTGGCA T C NDUFC2-KCTD14,NDUFC2 Ensembl:ENSG00000259112,Ensembl:ENSG00000151366 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs902788893 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95576,RMVar_hsa_circ_152009 21991 RMVar_ID_21991 Human_SNP_ID_473289324 A-to-I Human chr11 - 78069090 78069090 78069090 GAGCCCAGGAGTTCGAGACCAACTTGGGCAACATGGTGAAACACTGTCTCTACATAAAATACAAA GAGCCCAGGAGTTCGAGACCAACTTGGGCAACGTGGTGAAACACTGTCTCTACATAAAATACAAA T C NDUFC2-KCTD14,NDUFC2 Ensembl:ENSG00000259112,Ensembl:ENSG00000151366 Protein coding,Protein coding intron,3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1009479027 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95576,RMVar_hsa_circ_152009 21992 RMVar_ID_21992 Human_SNP_ID_473289325 A-to-I Human chr11 - 78069101 78069101 78069101 GCAGATTGCATGAGCCCAGGAGTTCGAGACCAACTTGGGCAACATGGTGAAACACTGTCTCTACA GCAGATTGCATGAGCCCAGGAGTTCGAGACCATCTTGGGCAACATGGTGAAACACTGTCTCTACA T A NDUFC2-KCTD14,NDUFC2 Ensembl:ENSG00000259112,Ensembl:ENSG00000151366 Protein coding,Protein coding intron,3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs546972049 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95576,RMVar_hsa_circ_152009 21993 RMVar_ID_21993 Human_SNP_ID_473289342 A-to-I Human chr11 - 78069179 78069179 78069179 TGGCTTATCAAATGCTTGTCCTGGCCCGATGCAGTGGCTCATGCCTGTAATCCCAGCACTTTGAG TGGCTTATCAAATGCTTGTCCTGGCCCGATGCTGTGGCTCATGCCTGTAATCCCAGCACTTTGAG T A NDUFC2-KCTD14,NDUFC2 Ensembl:ENSG00000259112,Ensembl:ENSG00000151366 Protein coding,Protein coding intron,3'UTR GSE38233;GSE100210;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 24183664,29129909,30559470 RNA-Seq:(High) rs532558534 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23522734 RMVar_hsa_circ_95576,RMVar_hsa_circ_152009 21994 RMVar_ID_21994 Human_SNP_ID_473291410 A-to-I Human chr11 - 78077716 78077716 78077716 CTGTCTCTACAAAAAAATTTAAAAAATTAGCCAGGCATGGTGATGTGCACTTGTAGTCCCAGGTA CTGTCTCTACAAAAAAATTTAAAAAATTAGCCCGGCATGGTGATGTGCACTTGTAGTCCCAGGTA T G NDUFC2-KCTD14,NDUFC2 Ensembl:ENSG00000259112,Ensembl:ENSG00000151366 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1201507054 Functional Loss SNV dbSNP153 33..33 33 - - - 21995 RMVar_ID_21995 Human_SNP_ID_473291696 A-to-I Human chr11 - 78078889 78078889 78078889 AAAACCCGTCCCTACAAAAAAATACAAAAGTTAGCCGGGCGTGGTGGTGCACGCCTGTGGTCCCA AAAACCCGTCCCTACAAAAAAATACAAAAGTTCGCCGGGCGTGGTGGTGCACGCCTGTGGTCCCA T G NDUFC2-KCTD14,NDUFC2 Ensembl:ENSG00000259112,Ensembl:ENSG00000151366 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1267210845 Functional Loss SNV dbSNP153 33..33 33 - - - 21996 RMVar_ID_21996 Human_SNP_ID_473298719 A-to-I Human chr11 - 78106258 78106258 78106258 GGGAGGAAGAGGTTGCAGTGAGCCGAGATCGCACCACTGCATTCCATTCTGGGTGACCGAAGGAG GGGAGGAAGAGGTTGCAGTGAGCCGAGATCGCGCCACTGCATTCCATTCTGGGTGACCGAAGGAG T C ALG8 Ensembl:ENSG00000159063 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1273273804 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101626,RMVar_hsa_circ_120766,RMVar_hsa_circ_125774,RMVar_hsa_circ_123498,RMVar_hsa_circ_107479,RMVar_hsa_circ_152015,RMVar_hsa_circ_89173,RMVar_hsa_circ_99557,RMVar_hsa_circ_93606,RMVar_hsa_circ_152019,RMVar_hsa_circ_83261,RMVar_hsa_circ_152017,RMVar_hsa_circ_152018,RMVar_hsa_circ_152016,RMVar_hsa_circ_152011,RMVar_hsa_circ_152013,RMVar_hsa_circ_152014,RMVar_hsa_circ_152012,RMVar_hsa_circ_152025,RMVar_hsa_circ_152026,RMVar_hsa_circ_152027,RMVar_hsa_circ_152024,RMVar_hsa_circ_40537,RMVar_hsa_circ_152028,RMVar_hsa_circ_75764,RMVar_hsa_circ_106805,RMVar_hsa_circ_152029,RMVar_hsa_circ_293730,RMVar_hsa_circ_320373,RMVar_hsa_circ_322065,RMVar_hsa_circ_339824,RMVar_hsa_circ_302531,RMVar_hsa_circ_152030,RMVar_hsa_circ_152032,RMVar_hsa_circ_152033,RMVar_hsa_circ_152031,RMVar_hsa_circ_152035,RMVar_hsa_circ_104622 21997 RMVar_ID_21997 Human_SNP_ID_473298728 A-to-I Human chr11 - 78106283 78106283 78106283 TGAGGCAGGAGAATTGCTTGAACCCGGGAGGAAGAGGTTGCAGTGAGCCGAGATCGCACCACTGC TGAGGCAGGAGAATTGCTTGAACCCGGGAGGAGGAGGTTGCAGTGAGCCGAGATCGCACCACTGC T C ALG8 Ensembl:ENSG00000159063 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1289606405 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101626,RMVar_hsa_circ_120766,RMVar_hsa_circ_125774,RMVar_hsa_circ_123498,RMVar_hsa_circ_107479,RMVar_hsa_circ_152015,RMVar_hsa_circ_89173,RMVar_hsa_circ_99557,RMVar_hsa_circ_93606,RMVar_hsa_circ_152019,RMVar_hsa_circ_83261,RMVar_hsa_circ_152017,RMVar_hsa_circ_152018,RMVar_hsa_circ_152016,RMVar_hsa_circ_152011,RMVar_hsa_circ_152013,RMVar_hsa_circ_152014,RMVar_hsa_circ_152012,RMVar_hsa_circ_152025,RMVar_hsa_circ_152026,RMVar_hsa_circ_152027,RMVar_hsa_circ_152024,RMVar_hsa_circ_40537,RMVar_hsa_circ_152028,RMVar_hsa_circ_75764,RMVar_hsa_circ_106805,RMVar_hsa_circ_152029,RMVar_hsa_circ_293730,RMVar_hsa_circ_320373,RMVar_hsa_circ_322065,RMVar_hsa_circ_339824,RMVar_hsa_circ_302531,RMVar_hsa_circ_152030,RMVar_hsa_circ_152032,RMVar_hsa_circ_152033,RMVar_hsa_circ_152031,RMVar_hsa_circ_152035,RMVar_hsa_circ_104622 21998 RMVar_ID_21998 Human_SNP_ID_473299166 A-to-I Human chr11 - 78107714 78107714 78107714 CCTCAGCCTCCAGAGTACCTGGGAATACAGGTATGTACCACCACGCCCAGCTAGTTTTTTTTGTA CCTCAGCCTCCAGAGTACCTGGGAATACAGGTGTGTACCACCACGCCCAGCTAGTTTTTTTTGTA T C ALG8 Ensembl:ENSG00000159063 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1478283552 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1281952 RMVar_hsa_circ_101626,RMVar_hsa_circ_125774,RMVar_hsa_circ_123498,RMVar_hsa_circ_107479,RMVar_hsa_circ_11592,RMVar_hsa_circ_152015,RMVar_hsa_circ_89173,RMVar_hsa_circ_99557,RMVar_hsa_circ_93606,RMVar_hsa_circ_83261,RMVar_hsa_circ_152017,RMVar_hsa_circ_152018,RMVar_hsa_circ_152016,RMVar_hsa_circ_152011,RMVar_hsa_circ_152013,RMVar_hsa_circ_152014,RMVar_hsa_circ_152012,RMVar_hsa_circ_152025,RMVar_hsa_circ_152026,RMVar_hsa_circ_152027,RMVar_hsa_circ_40537,RMVar_hsa_circ_152028,RMVar_hsa_circ_75764,RMVar_hsa_circ_106805,RMVar_hsa_circ_152029,RMVar_hsa_circ_293730,RMVar_hsa_circ_320373,RMVar_hsa_circ_322065,RMVar_hsa_circ_339824,RMVar_hsa_circ_152030,RMVar_hsa_circ_152032,RMVar_hsa_circ_152031,RMVar_hsa_circ_152035,RMVar_hsa_circ_104622,RMVar_hsa_circ_353546,RMVar_hsa_circ_359366,RMVar_hsa_circ_309791,RMVar_hsa_circ_152036,RMVar_hsa_circ_152037 21999 RMVar_ID_21999 Human_SNP_ID_473299207 A-to-I Human chr11 - 78107790 78107790 78107790 TCACCTAGGCTGGAGTGCAGTGGCGCAATTTCAGCTCACTGCAACCTCTGCCTCCCAGGTTCAAG TCACCTAGGCTGGAGTGCAGTGGCGCAATTTCGGCTCACTGCAACCTCTGCCTCCCAGGTTCAAG T C ALG8 Ensembl:ENSG00000159063 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1382417613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1281953 RMVar_hsa_circ_101626,RMVar_hsa_circ_125774,RMVar_hsa_circ_123498,RMVar_hsa_circ_107479,RMVar_hsa_circ_11592,RMVar_hsa_circ_152015,RMVar_hsa_circ_89173,RMVar_hsa_circ_99557,RMVar_hsa_circ_93606,RMVar_hsa_circ_83261,RMVar_hsa_circ_152017,RMVar_hsa_circ_152018,RMVar_hsa_circ_152016,RMVar_hsa_circ_152011,RMVar_hsa_circ_152013,RMVar_hsa_circ_152014,RMVar_hsa_circ_152012,RMVar_hsa_circ_152025,RMVar_hsa_circ_152026,RMVar_hsa_circ_152027,RMVar_hsa_circ_40537,RMVar_hsa_circ_152028,RMVar_hsa_circ_75764,RMVar_hsa_circ_106805,RMVar_hsa_circ_152029,RMVar_hsa_circ_293730,RMVar_hsa_circ_320373,RMVar_hsa_circ_322065,RMVar_hsa_circ_339824,RMVar_hsa_circ_152030,RMVar_hsa_circ_152032,RMVar_hsa_circ_152031,RMVar_hsa_circ_152035,RMVar_hsa_circ_104622,RMVar_hsa_circ_353546,RMVar_hsa_circ_359366,RMVar_hsa_circ_309791,RMVar_hsa_circ_152036,RMVar_hsa_circ_152037 22000 RMVar_ID_22000 Human_SNP_ID_473303250 A-to-I Human chr11 - 78122524 78122524 78122524 CAGCCTGGATAACATGGTGAAACCCTGCCTCTACTAAAAATACAAAAATTAGCCAGCTGTGGTTG CAGCCTGGATAACATGGTGAAACCCTGCCTCTCCTAAAAATACAAAAATTAGCCAGCTGTGGTTG T G ALG8 Ensembl:ENSG00000159063 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1444412404 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125774,RMVar_hsa_circ_107479,RMVar_hsa_circ_152011,RMVar_hsa_circ_152012,RMVar_hsa_circ_152027,RMVar_hsa_circ_75764,RMVar_hsa_circ_152029,RMVar_hsa_circ_320373,RMVar_hsa_circ_339824,RMVar_hsa_circ_152030,RMVar_hsa_circ_309791,RMVar_hsa_circ_53909,RMVar_hsa_circ_152037,RMVar_hsa_circ_327355,RMVar_hsa_circ_152042,RMVar_hsa_circ_152044,RMVar_hsa_circ_318802,RMVar_hsa_circ_318112,RMVar_hsa_circ_314167,RMVar_hsa_circ_152043,RMVar_hsa_circ_307985,RMVar_hsa_circ_27181,RMVar_hsa_circ_69453,RMVar_hsa_circ_282706,RMVar_hsa_circ_283923,RMVar_hsa_circ_113501,RMVar_hsa_circ_152051,RMVar_hsa_circ_152052 22001 RMVar_ID_22001 Human_SNP_ID_473303708 A-to-I Human chr11 - 78124138 78124138 78124138 GTTTGAGTATATCCTGTCACATGTTGCCAAATATTTTGATCAAGAAATGCTGAATGTCCATAATT GTTTGAGTATATCCTGTCACATGTTGCCAAATGTTTTGATCAAGAAATGCTGAATGTCCATAATT T C ALG8 Ensembl:ENSG00000159063 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs61995921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_31073,Human_RBP_ID_404404,Human_RBP_ID_1782919,Human_RBP_ID_2286631,Human_RBP_ID_11727003,Human_RBP_ID_22434767,Human_RBP_ID_22753780,Human_RBP_ID_23522822,Human_RBP_ID_24904480 Human_Splice_Rec_1281836,Human_Splice_Rec_1281858,Human_Splice_Rec_1281882,Human_Splice_Rec_1281928,Human_Splice_Rec_1281966,Human_Splice_Rec_1281978,Human_Splice_Rec_1281990,Human_Splice_Rec_1282002,Human_Splice_Rec_1282016,Human_Splice_Rec_1282026,Human_Splice_Rec_1282034 Clinvar_Rec_82 RMVar_hsa_circ_125774,RMVar_hsa_circ_107479,RMVar_hsa_circ_152011,RMVar_hsa_circ_152012,RMVar_hsa_circ_152027,RMVar_hsa_circ_75764,RMVar_hsa_circ_152029,RMVar_hsa_circ_320373,RMVar_hsa_circ_339824,RMVar_hsa_circ_152030,RMVar_hsa_circ_309791,RMVar_hsa_circ_53909,RMVar_hsa_circ_152037,RMVar_hsa_circ_327355,RMVar_hsa_circ_152042,RMVar_hsa_circ_152044,RMVar_hsa_circ_318802,RMVar_hsa_circ_318112,RMVar_hsa_circ_314167,RMVar_hsa_circ_152043,RMVar_hsa_circ_307985,RMVar_hsa_circ_27181,RMVar_hsa_circ_69453,RMVar_hsa_circ_282706,RMVar_hsa_circ_283923,RMVar_hsa_circ_113501,RMVar_hsa_circ_152051,RMVar_hsa_circ_152052,RMVar_hsa_circ_152053,RMVar_hsa_circ_372067 22002 RMVar_ID_22002 Human_SNP_ID_473303786 A-to-I Human chr11 - 78124420 78124420 78124420 TTTTTAATTAAAAATAGAGACAGGGTTTTACCATGTTGCCCAGACTGGTCTTGAACTCCTGGGCT TTTTTAATTAAAAATAGAGACAGGGTTTTACCGTGTTGCCCAGACTGGTCTTGAACTCCTGGGCT T C ALG8 Ensembl:ENSG00000159063 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs981114782 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125774,RMVar_hsa_circ_152011,RMVar_hsa_circ_75764,RMVar_hsa_circ_152029,RMVar_hsa_circ_320373,RMVar_hsa_circ_53909,RMVar_hsa_circ_318802,RMVar_hsa_circ_314167,RMVar_hsa_circ_152043,RMVar_hsa_circ_69453,RMVar_hsa_circ_283923,RMVar_hsa_circ_113501,RMVar_hsa_circ_152052,RMVar_hsa_circ_152053,RMVar_hsa_circ_372067 22003 RMVar_ID_22003 Human_SNP_ID_473303787 A-to-I Human chr11 - 78124420 78124420 78124420 TTTTTAATTAAAAATAGAGACAGGGTTTTACCATGTTGCCCAGACTGGTCTTGAACTCCTGGGCT TTTTTAATTAAAAATAGAGACAGGGTTTTACCCTGTTGCCCAGACTGGTCTTGAACTCCTGGGCT T G ALG8 Ensembl:ENSG00000159063 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs981114782 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125774,RMVar_hsa_circ_152011,RMVar_hsa_circ_75764,RMVar_hsa_circ_152029,RMVar_hsa_circ_320373,RMVar_hsa_circ_53909,RMVar_hsa_circ_318802,RMVar_hsa_circ_314167,RMVar_hsa_circ_152043,RMVar_hsa_circ_69453,RMVar_hsa_circ_283923,RMVar_hsa_circ_113501,RMVar_hsa_circ_152052,RMVar_hsa_circ_152053,RMVar_hsa_circ_372067 22004 RMVar_ID_22004 Human_SNP_ID_473304160 A-to-I Human chr11 - 78125770 78125770 78125770 CGAAGTCTCACTCTCACCCAGGCCGGAGTGCAATGGCACGATCTCGGCTGACTGGCGACCTCTGC CGAAGTCTCACTCTCACCCAGGCCGGAGTGCAGTGGCACGATCTCGGCTGACTGGCGACCTCTGC T C ALG8 Ensembl:ENSG00000159063 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1369206390 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11727019 RMVar_hsa_circ_125774,RMVar_hsa_circ_152011,RMVar_hsa_circ_75764,RMVar_hsa_circ_152029,RMVar_hsa_circ_320373,RMVar_hsa_circ_53909,RMVar_hsa_circ_318802,RMVar_hsa_circ_314167,RMVar_hsa_circ_152043,RMVar_hsa_circ_69453,RMVar_hsa_circ_283923,RMVar_hsa_circ_113501,RMVar_hsa_circ_152052,RMVar_hsa_circ_152053,RMVar_hsa_circ_372067 22005 RMVar_ID_22005 Human_SNP_ID_473304796 A-to-I Human chr11 - 78127858 78127858 78127858 ACCTCTACTAAAAATTAGCCAGGATTGGTGGTACATGCCTGTAGTCTCAGCTGCTCGGGAGGCTG ACCTCTACTAAAAATTAGCCAGGATTGGTGGTGCATGCCTGTAGTCTCAGCTGCTCGGGAGGCTG T C ALG8 Ensembl:ENSG00000159063 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1018654476 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125774,RMVar_hsa_circ_152011,RMVar_hsa_circ_113501,RMVar_hsa_circ_152052 22006 RMVar_ID_22006 Human_SNP_ID_473306446 A-to-I Human chr11 - 78133778 78133778 78133778 TCTGCCTCAGCCTACCGAGTAGCTGACCCTACAGGCGCCCCTCACCAAGCCCGGCTAATTTTTTT TCTGCCTCAGCCTACCGAGTAGCTGACCCTACCGGCGCCCCTCACCAAGCCCGGCTAATTTTTTT T G ALG8 Ensembl:ENSG00000159063 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1321783668 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125774,RMVar_hsa_circ_152011,RMVar_hsa_circ_113501,RMVar_hsa_circ_152052 22007 RMVar_ID_22007 Human_SNP_ID_473306590 A-to-I Human chr11 - 78134266 78134266 78134266 AAGTGTGGTGGTGGGCACCTGTGATCCCAGCCACTTAGGAGGCTGAGGCAGGAGAATCACTTGAA AAGTGTGGTGGTGGGCACCTGTGATCCCAGCCGCTTAGGAGGCTGAGGCAGGAGAATCACTTGAA T C ALG8 Ensembl:ENSG00000159063 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs537447259 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125774,RMVar_hsa_circ_152011,RMVar_hsa_circ_113501,RMVar_hsa_circ_152052 22008 RMVar_ID_22008 Human_SNP_ID_473306591 A-to-I Human chr11 - 78134266 78134266 78134266 AAGTGTGGTGGTGGGCACCTGTGATCCCAGCCACTTAGGAGGCTGAGGCAGGAGAATCACTTGAA AAGTGTGGTGGTGGGCACCTGTGATCCCAGCCCCTTAGGAGGCTGAGGCAGGAGAATCACTTGAA T G ALG8 Ensembl:ENSG00000159063 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs537447259 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125774,RMVar_hsa_circ_152011,RMVar_hsa_circ_113501,RMVar_hsa_circ_152052 22009 RMVar_ID_22009 Human_SNP_ID_473306623 A-to-I Human chr11 - 78134375 78134375 78134375 CCAGCGTTTTGGGAGGCTGAGGCGGGCGGGTCACCTGAGGTCAGGAGTTCAAGACCCGCCTGGCC CCAGCGTTTTGGGAGGCTGAGGCGGGCGGGTCTCCTGAGGTCAGGAGTTCAAGACCCGCCTGGCC T A ALG8 Ensembl:ENSG00000159063 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1419088909 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125774,RMVar_hsa_circ_152011,RMVar_hsa_circ_113501,RMVar_hsa_circ_152052 22010 RMVar_ID_22010 Human_SNP_ID_473306823 A-to-I Human chr11 - 78135254 78135254 78135254 ACCTTTCAGGCTCAAGCAATCCTCCTACCTCAACCTGCCAAGTAGCTGGGACTTAAGGTGTGTGC ACCTTTCAGGCTCAAGCAATCCTCCTACCTCAGCCTGCCAAGTAGCTGGGACTTAAGGTGTGTGC T C ALG8 Ensembl:ENSG00000159063 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1012168896 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1282012,Human_Splice_Rec_1282013,Human_Splice_Rec_1282038 RMVar_hsa_circ_125774,RMVar_hsa_circ_152011,RMVar_hsa_circ_113501,RMVar_hsa_circ_152052 22011 RMVar_ID_22011 Human_SNP_ID_473306827 A-to-I Human chr11 - 78135268 78135268 78135268 TCACTGCAACCTCCACCTTTCAGGCTCAAGCAATCCTCCTACCTCAACCTGCCAAGTAGCTGGGA TCACTGCAACCTCCACCTTTCAGGCTCAAGCAGTCCTCCTACCTCAACCTGCCAAGTAGCTGGGA T C ALG8 Ensembl:ENSG00000159063 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1466488073 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1282012,Human_Splice_Rec_1282013,Human_Splice_Rec_1282038 RMVar_hsa_circ_125774,RMVar_hsa_circ_152011,RMVar_hsa_circ_113501,RMVar_hsa_circ_152052 22012 RMVar_ID_22012 Human_SNP_ID_473307073 A-to-I Human chr11 - 78136118 78136118 78136118 TTTGTCAGGCTGGAGTGCACTGGTATGATCTCAGCTCACTGCTGCCTCTACTTCCTGGGCTCAAA TTTGTCAGGCTGGAGTGCACTGGTATGATCTCGGCTCACTGCTGCCTCTACTTCCTGGGCTCAAA T C ALG8 Ensembl:ENSG00000159063 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs553735469 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6098038,Human_RBP_ID_8359762,Human_RBP_ID_11727287 RMVar_hsa_circ_125774,RMVar_hsa_circ_152011,RMVar_hsa_circ_113501,RMVar_hsa_circ_152052 22013 RMVar_ID_22013 Human_SNP_ID_473307083 A-to-I Human chr11 - 78136160 78136160 78136160 ATATTTTTCCTTTTTCTTTTCTTTTTTGAGACAGTGTTTCACTTTGTCAGGCTGGAGTGCACTGG ATATTTTTCCTTTTTCTTTTCTTTTTTGAGACGGTGTTTCACTTTGTCAGGCTGGAGTGCACTGG T C ALG8 Ensembl:ENSG00000159063 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1050795338 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2286668,Human_RBP_ID_11727293 RMVar_hsa_circ_125774,RMVar_hsa_circ_152011,RMVar_hsa_circ_113501,RMVar_hsa_circ_152052 22014 RMVar_ID_22014 Human_SNP_ID_473307336 A-to-I Human chr11 - 78137080 78137080 78137080 GAGGACCAACATGGAGAAATCTCGTCTCTACTAAAAATACAAAATTAGCTGGGCGTGGTGGAGCA GAGGACCAACATGGAGAAATCTCGTCTCTACTGAAAATACAAAATTAGCTGGGCGTGGTGGAGCA T C ALG8 Ensembl:ENSG00000159063 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs769617330 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6098050 RMVar_hsa_circ_125774,RMVar_hsa_circ_152011,RMVar_hsa_circ_113501,RMVar_hsa_circ_152052 22015 RMVar_ID_22015 Human_SNP_ID_473308691 A-to-I Human chr11 + 78141995 78141995 78141995 TCGGCTCACTGAAGCCTCTGCTTCCCGGGTTTAAGAAATTCTCTGCCTCAGCCTCCCAAGTAGCT TCGGCTCACTGAAGCCTCTGCTTCCCGGGTTTGAGAAATTCTCTGCCTCAGCCTCCCAAGTAGCT A G KCTD21-AS1 Ensembl:ENSG00000246174 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1181493271 Functional Loss SNV dbSNP153 33..33 33 - - - 22016 RMVar_ID_22016 Human_SNP_ID_473334967 A-to-I Human chr11 - 78231416 78231416 78231416 TGAACCCAGGAGGCGGAGGTTGCAGTGAGCCAAGATTGCATCACTGCACTCCAGCCTGGGAGACA TGAACCCAGGAGGCGGAGGTTGCAGTGAGCCAGGATTGCATCACTGCACTCCAGCCTGGGAGACA T C GAB2 Ensembl:ENSG00000033327 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913747260 Functional Loss SNV dbSNP153 33..33 33 - - - 22017 RMVar_ID_22017 Human_SNP_ID_473334968 A-to-I Human chr11 - 78231416 78231416 78231416 TGAACCCAGGAGGCGGAGGTTGCAGTGAGCCAAGATTGCATCACTGCACTCCAGCCTGGGAGACA TGAACCCAGGAGGCGGAGGTTGCAGTGAGCCACGATTGCATCACTGCACTCCAGCCTGGGAGACA T G GAB2 Ensembl:ENSG00000033327 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913747260 Functional Loss SNV dbSNP153 33..33 33 - - - 22018 RMVar_ID_22018 Human_SNP_ID_473345175 A-to-I Human chr11 - 78270245 78270245 78270245 ACTGCAACCTCCACCCTCCACCTCCCGGGTTCAGGCGATTCTCCTGCCTCGGCCTCCTGAGTAGC ACTGCAACCTCCACCCTCCACCTCCCGGGTTCGGGCGATTCTCCTGCCTCGGCCTCCTGAGTAGC T C GAB2 Ensembl:ENSG00000033327 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1165430757 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_108360 RMVar_hsa_circ_120932,RMVar_hsa_circ_152063,RMVar_hsa_circ_96826,RMVar_hsa_circ_152064 22019 RMVar_ID_22019 Human_SNP_ID_473389476 A-to-I Human chr11 - 78437892 78437892 78437892 CTGCTCACTGCAACCTCCACTTCCCAGGTTCAAGCGACTCCTCTGCCTCAGCCTCCTGAGTAGCT CTGCTCACTGCAACCTCCACTTCCCAGGTTCAGGCGACTCCTCTGCCTCAGCCTCCTGAGTAGCT T C NARS2 Ensembl:ENSG00000137513 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs545812924 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99264,RMVar_hsa_circ_108624,RMVar_hsa_circ_152067,RMVar_hsa_circ_152068 22020 RMVar_ID_22020 Human_SNP_ID_473390448 A-to-I Human chr11 - 78441628 78441628 78441628 TGGTTCACTGCAACTTCTGCCTCCTAGGTTCAAGCAATCCTTCTACCTCAGCTTCCCGAGTAGCT TGGTTCACTGCAACTTCTGCCTCCTAGGTTCAGGCAATCCTTCTACCTCAGCTTCCCGAGTAGCT T C NARS2 Ensembl:ENSG00000137513 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs532481698 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104916,RMVar_hsa_circ_99264,RMVar_hsa_circ_108624,RMVar_hsa_circ_152067,RMVar_hsa_circ_152068,RMVar_hsa_circ_344406,RMVar_hsa_circ_152069,RMVar_hsa_circ_152070 22021 RMVar_ID_22021 Human_SNP_ID_473411824 A-to-I Human chr11 - 78519821 78519821 78519821 TGGCATGCGCCTGTAGTCCCAGCTACTCGGGAAGCTGAGGCAGGAGAATCGCGTGAACCCAGGAG TGGCATGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCGTGAACCCAGGAG T C NARS2 Ensembl:ENSG00000137513 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1038874348 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_108999 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 22022 RMVar_ID_22022 Human_SNP_ID_473411832 A-to-I Human chr11 - 78519829 78519829 78519829 AGGCGTGGTGGCATGCGCCTGTAGTCCCAGCTACTCGGGAAGCTGAGGCAGGAGAATCGCGTGAA AGGCGTGGTGGCATGCGCCTGTAGTCCCAGCTGCTCGGGAAGCTGAGGCAGGAGAATCGCGTGAA T C NARS2 Ensembl:ENSG00000137513 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1170969301 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_108999 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 22023 RMVar_ID_22023 Human_SNP_ID_473412259 A-to-I Human chr11 - 78521275 78521275 78521275 CTGTAGTCCTAGCTACTTGGGAGAGTAAGGCAAGAAGATTGCTGGAGCCCAGGAGTTGTAGACTG CTGTAGTCCTAGCTACTTGGGAGAGTAAGGCAGGAAGATTGCTGGAGCCCAGGAGTTGTAGACTG T C NARS2 Ensembl:ENSG00000137513 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1238607281 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11728515 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 22024 RMVar_ID_22024 Human_SNP_ID_434386612 A-to-I Human chr10 - 60045251 60045251 60045251 TAACAAATCAGAAAGCCAGATTCTAACTCTGTATTACTGGAATGTAAAAGATAGTGACTCTGATA TAACAAATCAGAAAGCCAGATTCTAACTCTGTGTTACTGGAATGTAAAAGATAGTGACTCTGATA T C ANK3 Ensembl:ENSG00000151150 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1473563341 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51831,RMVar_hsa_circ_278129,RMVar_hsa_circ_329275,RMVar_hsa_circ_275656,RMVar_hsa_circ_143528,RMVar_hsa_circ_143529 22025 RMVar_ID_22025 Human_SNP_ID_434386714 A-to-I Human chr10 - 60045752 60045752 60045752 TGGCTGGCACTGACCAAATTATCAGAGCCACTATCTTTTCCATGCCAGTAACACAAAGAGTTAGA TGGCTGGCACTGACCAAATTATCAGAGCCACTGTCTTTTCCATGCCAGTAACACAAAGAGTTAGA T C ANK3 Ensembl:ENSG00000151150 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1416250748 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51831,RMVar_hsa_circ_278129,RMVar_hsa_circ_329275,RMVar_hsa_circ_275656,RMVar_hsa_circ_143528,RMVar_hsa_circ_143529 22026 RMVar_ID_22026 Human_SNP_ID_434386772 A-to-I Human chr10 - 60045946 60045944 60045946 TGAACTATGCACCCACAAACTGTAAGAACACAAAGTCACTTTGTAATAAGAAAAAAAAAAAATGA TGAACTATGCACCCACAAACTGTAAGAACACA__GTCACTTTGTAATAAGAAAAAAAAAAAATGA CTT C ANK3 Ensembl:ENSG00000151150 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1167406759 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_8990008 RMVar_hsa_circ_51831,RMVar_hsa_circ_278129,RMVar_hsa_circ_329275,RMVar_hsa_circ_275656,RMVar_hsa_circ_143528,RMVar_hsa_circ_143529 22027 RMVar_ID_22027 Human_SNP_ID_434402794 A-to-I Human chr10 - 60108877 60108877 60108877 AACCCACCCCCCATGGTGGAAGGAGAGGGATTAGCCAGTAGGCTGGTAGAAATGGGTCCTGCAGG AACCCACCCCCCATGGTGGAAGGAGAGGGATTCGCCAGTAGGCTGGTAGAAATGGGTCCTGCAGG T G ANK3 Ensembl:ENSG00000151150 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1164688644 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4122511,Human_RBP_ID_8765311 Human_Splice_Rec_1136537,Human_Splice_Rec_1136625,Human_Splice_Rec_1136691,Human_Splice_Rec_1136793,Human_Splice_Rec_1136869,Human_Splice_Rec_1137001,Human_Splice_Rec_1137015,Human_Splice_Rec_1137029 Human_miRNA_ID_334491,Human_miRNA_ID_792904 RMVar_hsa_circ_164,RMVar_hsa_circ_353506,RMVar_hsa_circ_71224,RMVar_hsa_circ_267877,RMVar_hsa_circ_59684,RMVar_hsa_circ_143536,RMVar_hsa_circ_93651,RMVar_hsa_circ_313321,RMVar_hsa_circ_143538,RMVar_hsa_circ_34137,RMVar_hsa_circ_5896,RMVar_hsa_circ_13114,RMVar_hsa_circ_321080,RMVar_hsa_circ_328359,RMVar_hsa_circ_353161,RMVar_hsa_circ_275802,RMVar_hsa_circ_298449,RMVar_hsa_circ_37794,RMVar_hsa_circ_143543,RMVar_hsa_circ_143544,RMVar_hsa_circ_143545,RMVar_hsa_circ_143542,RMVar_hsa_circ_345336 22028 RMVar_ID_22028 Human_SNP_ID_434461563 A-to-I Human chr10 - 60352244 60352244 60352244 CCAGGCTGGATGGAGTACAGTGGCGTGATCACAGCTCACTGCACCCCTCCGCCTCCTGGGCTCAA CCAGGCTGGATGGAGTACAGTGGCGTGATCACCGCTCACTGCACCCCTCCGCCTCCTGGGCTCAA T G ANK3 Ensembl:ENSG00000151150 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1044561942 Functional Loss SNV dbSNP153 33..33 33 - - - 22029 RMVar_ID_22029 Human_SNP_ID_434481597 A-to-I Human chr10 - 60432823 60432823 60432823 TCTCAGAACAGCAGCAGAGCCACAGTGGGATAATTTCACTTGGTAAGAACTTGTCATGCTCTCCT TCTCAGAACAGCAGCAGAGCCACAGTGGGATACTTTCACTTGGTAAGAACTTGTCATGCTCTCCT T G ANK3 Ensembl:ENSG00000151150 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1358706520 Functional Loss SNV dbSNP153 33..33 33 - - - 22030 RMVar_ID_22030 Human_SNP_ID_434489445 A-to-I Human chr10 - 60465200 60465200 60465200 GAGACTGGAGTGCAGTGGGGCAATCATGGCTCACTGCAGCCTCAAATTCTCAGGTTCAGGTGATC GAGACTGGAGTGCAGTGGGGCAATCATGGCTCCCTGCAGCCTCAAATTCTCAGGTTCAGGTGATC T G ANK3 Ensembl:ENSG00000151150 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs554826575 Functional Loss SNV dbSNP153 33..33 33 - - - 22031 RMVar_ID_22031 Human_SNP_ID_434848117 A-to-I Human chr10 + 61921921 61921921 61921921 CGGAGTGCAGTAGTGTGACCACGGCTCACTGCAGCCTCGACCTCCCTGGCTCAAGCGATCCTCCC CGGAGTGCAGTAGTGTGACCACGGCTCACTGCGGCCTCGACCTCCCTGGCTCAAGCGATCCTCCC A G ARID5B Ensembl:ENSG00000150347 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1564602295 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114319,RMVar_hsa_circ_143580 22032 RMVar_ID_22032 Human_SNP_ID_434854688 A-to-I Human chr10 + 61949379 61949379 61949379 ATGATGGAGGCTGGGCACGGTGGCTCACGCCTATAATCCCAACACTTTGGGAGGCCAAGGCAGGT ATGATGGAGGCTGGGCACGGTGGCTCACGCCTGTAATCCCAACACTTTGGGAGGCCAAGGCAGGT A G ARID5B Ensembl:ENSG00000150347 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1234068536 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108257,RMVar_hsa_circ_114319,RMVar_hsa_circ_349513,RMVar_hsa_circ_143580,RMVar_hsa_circ_363560,RMVar_hsa_circ_337196,RMVar_hsa_circ_143582,RMVar_hsa_circ_143583 22033 RMVar_ID_22033 Human_SNP_ID_434854954 A-to-I Human chr10 + 61950487 61950487 61950487 GGCCAGGAGTTCAAGAGGAACCTGGGCAACATAGTGAGACCTGTCTCTGCAAAAAAATTTTAAAA GGCCAGGAGTTCAAGAGGAACCTGGGCAACATGGTGAGACCTGTCTCTGCAAAAAAATTTTAAAA A G ARID5B Ensembl:ENSG00000150347 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1227519617 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108257,RMVar_hsa_circ_114319,RMVar_hsa_circ_349513,RMVar_hsa_circ_143580,RMVar_hsa_circ_363560,RMVar_hsa_circ_337196,RMVar_hsa_circ_143582,RMVar_hsa_circ_143583 22034 RMVar_ID_22034 Human_SNP_ID_434868210 A-to-I Human chr10 + 62008198 62008198 62008198 CAACAGAGCAGTACCCAGCACATAGTAGCTGTAGTAAATATTGGTTACATGAATGGATGGATACG CAACAGAGCAGTACCCAGCACATAGTAGCTGTGGTAAATATTGGTTACATGAATGGATGGATACG A G ARID5B Ensembl:ENSG00000150347 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1257929491 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115167,RMVar_hsa_circ_108257,RMVar_hsa_circ_114319,RMVar_hsa_circ_143580,RMVar_hsa_circ_363560,RMVar_hsa_circ_337196,RMVar_hsa_circ_143583,RMVar_hsa_circ_341387,RMVar_hsa_circ_342327,RMVar_hsa_circ_143585 22035 RMVar_ID_22035 Human_SNP_ID_434883536 A-to-I Human chr10 + 62076421 62076421 62076421 ACAATTAGCTGGGGCTGGTGGCACACACCTGTAATCCTGACTACTCAGATGTCTGAGGCACGAGA ACAATTAGCTGGGGCTGGTGGCACACACCTGTCATCCTGACTACTCAGATGTCTGAGGCACGAGA A C ARID5B Ensembl:ENSG00000150347 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1325146242 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268529,RMVar_hsa_circ_360804 22036 RMVar_ID_22036 Human_SNP_ID_434885853 A-to-I Human chr10 + 62086793 62086793 62086793 GAGGTGGGAGGATAACCAGAGCCCTGGGAGGTAAAGTCTGCAGTGAGCTGTGATTATACCACTGC GAGGTGGGAGGATAACCAGAGCCCTGGGAGGTGAAGTCTGCAGTGAGCTGTGATTATACCACTGC A G ARID5B Ensembl:ENSG00000150347 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs575747191 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268529 22037 RMVar_ID_22037 Human_SNP_ID_434886614 A-to-I Human chr10 + 62089614 62089614 62089614 CAATGGCATGATCTCGGCTCACCGCATCCTCCACCTCTGGGGTTCAAGCGATTCTCCTGCCTCAG CAATGGCATGATCTCGGCTCACCGCATCCTCCGCCTCTGGGGTTCAAGCGATTCTCCTGCCTCAG A G ARID5B Ensembl:ENSG00000150347 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1362814363 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268529 22038 RMVar_ID_22038 Human_SNP_ID_434913528 A-to-I Human chr10 - 62202917 62202917 62202917 ACCTCAGGTGATCCGCCCACCTCAGCCCCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCAC ACCTCAGGTGATCCGCCCACCTCAGCCCCCCATAGTGCTGGGATTACAGGTGTGAGCCACCGCAC T A RTKN2 Ensembl:ENSG00000182010 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs943761768 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61404,RMVar_hsa_circ_304955,RMVar_hsa_circ_321845,RMVar_hsa_circ_66286 22039 RMVar_ID_22039 Human_SNP_ID_434913529 A-to-I Human chr10 - 62202917 62202917 62202917 ACCTCAGGTGATCCGCCCACCTCAGCCCCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCAC ACCTCAGGTGATCCGCCCACCTCAGCCCCCCAGAGTGCTGGGATTACAGGTGTGAGCCACCGCAC T C RTKN2 Ensembl:ENSG00000182010 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs943761768 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61404,RMVar_hsa_circ_304955,RMVar_hsa_circ_321845,RMVar_hsa_circ_66286 22040 RMVar_ID_22040 Human_SNP_ID_435141789 A-to-I Human chr10 + 63135112 63135112 63135112 GGGAGGCTGAGGTGGCAGGATCGCTTGAGCCCAGGAGGTGGAGGTTGCAGTGGGCCGAGATTGTG GGGAGGCTGAGGTGGCAGGATCGCTTGAGCCCGGGAGGTGGAGGTTGCAGTGGGCCGAGATTGTG A G NRBF2 Ensembl:ENSG00000148572 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs909044283 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126098,RMVar_hsa_circ_143591 22041 RMVar_ID_22041 Human_SNP_ID_435143102 A-to-I Human chr10 + 63140553 63140553 63140553 TCCTCCTACCAGTCCCTCCTGTAGCTGGGACTACAGGTGTGCACCACTACACCCAGCTAATTTTT TCCTCCTACCAGTCCCTCCTGTAGCTGGGACTGCAGGTGTGCACCACTACACCCAGCTAATTTTT A G NRBF2 Ensembl:ENSG00000148572 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1279096969 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126098,RMVar_hsa_circ_143591 22042 RMVar_ID_22042 Human_SNP_ID_435143107 A-to-I Human chr10 + 63140579 63140579 63140579 GGGACTACAGGTGTGCACCACTACACCCAGCTAATTTTTCTATTTTTTGTAGAGATGGGGTCTCA GGGACTACAGGTGTGCACCACTACACCCAGCTGATTTTTCTATTTTTTGTAGAGATGGGGTCTCA A G NRBF2 Ensembl:ENSG00000148572 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1404361097 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126098,RMVar_hsa_circ_143591 22043 RMVar_ID_22043 Human_SNP_ID_435152952 A-to-I Human chr10 - 63179585 63179585 63179585 TATTTTTTTGTAAAGACGGGTTTTACCATGTTACTCAGGCTGGTCTCAAACTCCTGGGCTCAAGT TATTTTTTTGTAAAGACGGGTTTTACCATGTTGCTCAGGCTGGTCTCAAACTCCTGGGCTCAAGT T C JMJD1C Ensembl:ENSG00000171988 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1223681593 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9931,RMVar_hsa_circ_997,RMVar_hsa_circ_107684,RMVar_hsa_circ_143592,RMVar_hsa_circ_143598,RMVar_hsa_circ_279594,RMVar_hsa_circ_304911,RMVar_hsa_circ_329324,RMVar_hsa_circ_335156,RMVar_hsa_circ_301264,RMVar_hsa_circ_301919,RMVar_hsa_circ_283354,RMVar_hsa_circ_25346,RMVar_hsa_circ_48453,RMVar_hsa_circ_143600,RMVar_hsa_circ_143601,RMVar_hsa_circ_143599,RMVar_hsa_circ_90352,RMVar_hsa_circ_143596,RMVar_hsa_circ_143597,RMVar_hsa_circ_313931,RMVar_hsa_circ_45395,RMVar_hsa_circ_68260,RMVar_hsa_circ_35252,RMVar_hsa_circ_143602,RMVar_hsa_circ_143603 22044 RMVar_ID_22044 Human_SNP_ID_435164507 A-to-I Human chr10 - 63222247 63222247 63222247 ATCTCGACAGCTCTCCCTGTTACATCCTGTAAATCATCTTGATGCTTTTGAACCCCCCTATAAAT ATCTCGACAGCTCTCCCTGTTACATCCTGTAAGTCATCTTGATGCTTTTGAACCCCCCTATAAAT T C JMJD1C Ensembl:ENSG00000171988 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1185970367 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_68824,RMVar_hsa_circ_51781,RMVar_hsa_circ_24971,RMVar_hsa_circ_14996,RMVar_hsa_circ_328149 22045 RMVar_ID_22045 Human_SNP_ID_435172383 A-to-I Human chr10 - 63250292 63250292 63250292 ATTCTTTTGGCTTGGTGCAGTGGCTTAAGCCTATAATCCTACCACTTTAAGAGCCAAAGCAGGAG ATTCTTTTGGCTTGGTGCAGTGGCTTAAGCCTGTAATCCTACCACTTTAAGAGCCAAAGCAGGAG T C JMJD1C Ensembl:ENSG00000171988 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs938602528 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_68824,RMVar_hsa_circ_51781,RMVar_hsa_circ_24971,RMVar_hsa_circ_14996,RMVar_hsa_circ_328149 22046 RMVar_ID_22046 Human_SNP_ID_435173153 A-to-I Human chr10 - 63253495 63253495 63253495 CCTGTATTCCCAGCTACTCGGGAGTCTGAGGCAGGAGAATCGTTTGAGCCCGGGAGGCAGAGGTT CCTGTATTCCCAGCTACTCGGGAGTCTGAGGCCGGAGAATCGTTTGAGCCCGGGAGGCAGAGGTT T G JMJD1C Ensembl:ENSG00000171988 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1267646438 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_68824,RMVar_hsa_circ_51781,RMVar_hsa_circ_24971,RMVar_hsa_circ_14996,RMVar_hsa_circ_328149 22047 RMVar_ID_22047 Human_SNP_ID_435173598 A-to-I Human chr10 - 63255073 63255073 63255073 GGGAGGCCGAGGTGGGAGGATTGCTTGAGCTCAGGCATTTGAGACTGGGTAACATGGGAGAACCC GGGAGGCCGAGGTGGGAGGATTGCTTGAGCTCGGGCATTTGAGACTGGGTAACATGGGAGAACCC T C JMJD1C Ensembl:ENSG00000171988 Protein coding intron GSE100210;GSE107867;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank;ASD brains,temporal_cortex - 29129909,30559470,30559470 RNA-Seq:(High) rs550697731 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24820002 RMVar_hsa_circ_68824,RMVar_hsa_circ_51781,RMVar_hsa_circ_24971,RMVar_hsa_circ_14996,RMVar_hsa_circ_328149 22048 RMVar_ID_22048 Human_SNP_ID_435174774 A-to-I Human chr10 - 63260030 63260030 63260030 AATGATTCCATTAGAAGTTCTGGATCCCAGCTACTCTGGAGGCTGAGGCAAGAGAATCACTTGAA AATGATTCCATTAGAAGTTCTGGATCCCAGCTGCTCTGGAGGCTGAGGCAAGAGAATCACTTGAA T C JMJD1C Ensembl:ENSG00000171988 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1381144387 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5985820,Human_RBP_ID_11388165 RMVar_hsa_circ_68824,RMVar_hsa_circ_51781,RMVar_hsa_circ_24971,RMVar_hsa_circ_14996,RMVar_hsa_circ_328149 22049 RMVar_ID_22049 Human_SNP_ID_435177775 A-to-I Human chr10 - 63271317 63271317 63271317 CAAAAATTAGCCGGGCACGGTGGCGCGTGTCTATAGTCCCAGCTACTCTGGAGGCTGAGGCAGGA CAAAAATTAGCCGGGCACGGTGGCGCGTGTCTGTAGTCCCAGCTACTCTGGAGGCTGAGGCAGGA T C JMJD1C Ensembl:ENSG00000171988 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs997762987 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_307868 22050 RMVar_ID_22050 Human_SNP_ID_435177932 A-to-I Human chr10 - 63271870 63271870 63271870 GGGGTTTGCCATGATGGCCAGGCTGGTCTCAAACTCTTGACCTCAAGTGATCCACCCACCACTGA GGGGTTTGCCATGATGGCCAGGCTGGTCTCAATCTCTTGACCTCAAGTGATCCACCCACCACTGA T A JMJD1C Ensembl:ENSG00000171988 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1229978050 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_307868 22051 RMVar_ID_22051 Human_SNP_ID_435194530 A-to-I Human chr10 - 63329993 63329993 63329993 GGGAGGCTGAGACACGAGAATCTCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCCTAGATTGTA GGGAGGCTGAGACACGAGAATCTCTTGAACCCGGGAGGCGGAGGTTGCAGTGAGCCTAGATTGTA T C JMJD1C Ensembl:ENSG00000171988 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs922788799 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125595,RMVar_hsa_circ_307868,RMVar_hsa_circ_143631 22052 RMVar_ID_22052 Human_SNP_ID_435194978 A-to-I Human chr10 - 63331673 63331673 63331673 GGGAAGCAGAGGTTATAGTGAGCTGAGATTGCACCACTGTACTCCAGCCTGGGCAACAGAGCGAG GGGAAGCAGAGGTTATAGTGAGCTGAGATTGCTCCACTGTACTCCAGCCTGGGCAACAGAGCGAG T A JMJD1C Ensembl:ENSG00000171988 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1413818266 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125595,RMVar_hsa_circ_307868,RMVar_hsa_circ_143631 22053 RMVar_ID_22053 Human_SNP_ID_435197515 A-to-I Human chr10 - 63339997 63339997 63339997 GGAGTGCAGTGGCGCTATCTCAGCTCACTGCAACCTCCGCCTCCTGGGTTCAAGCATTTCTCCTG GGAGTGCAGTGGCGCTATCTCAGCTCACTGCAGCCTCCGCCTCCTGGGTTCAAGCATTTCTCCTG T C JMJD1C Ensembl:ENSG00000171988 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1473558843 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125595,RMVar_hsa_circ_307868,RMVar_hsa_circ_143631 22054 RMVar_ID_22054 Human_SNP_ID_435197517 A-to-I Human chr10 - 63340008 63340008 63340008 TCACCCAGGCTGGAGTGCAGTGGCGCTATCTCAGCTCACTGCAACCTCCGCCTCCTGGGTTCAAG TCACCCAGGCTGGAGTGCAGTGGCGCTATCTCGGCTCACTGCAACCTCCGCCTCCTGGGTTCAAG T C JMJD1C Ensembl:ENSG00000171988 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs796197365 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125595,RMVar_hsa_circ_307868,RMVar_hsa_circ_143631 22055 RMVar_ID_22055 Human_SNP_ID_435202508 A-to-I Human chr10 - 63358508 63358507 63358509 GATATATCTTAATTATATCGTATTAAAGAGACAGGATCTTGCTATATTGCCCAGGCTGGACTAGA GATATATCTTAATTATATCGTATTAAAGAGA__GGATCTTGCTATATTGCCCAGGCTGGACTAGA CTG C JMJD1C Ensembl:ENSG00000171988 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs906652718 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_11495457,Human_RBP_ID_24820671 RMVar_hsa_circ_125595,RMVar_hsa_circ_307868,RMVar_hsa_circ_143631 22056 RMVar_ID_22056 Human_SNP_ID_435202914 A-to-I Human chr10 - 63360116 63360116 63360116 TAAGAGATGGGGGATCTTGCTATGTTTCCCAAACTGGTCTTCAACTGTTGGCCTCTATTGATTCT TAAGAGATGGGGGATCTTGCTATGTTTCCCAAGCTGGTCTTCAACTGTTGGCCTCTATTGATTCT T C JMJD1C Ensembl:ENSG00000171988 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1219442864 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17559280,Human_RBP_ID_22883041 RMVar_hsa_circ_125595,RMVar_hsa_circ_307868,RMVar_hsa_circ_143631 22057 RMVar_ID_22057 Human_SNP_ID_435203230 A-to-I Human chr10 - 63361384 63361384 63361384 AGTCTTGCTCTTTTTGTCCAGACTGGAGTGCAATGGCGCAATCTCAGCTCACTGCAACCTCCGCC AGTCTTGCTCTTTTTGTCCAGACTGGAGTGCAGTGGCGCAATCTCAGCTCACTGCAACCTCCGCC T C JMJD1C Ensembl:ENSG00000171988 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs537108671 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125595,RMVar_hsa_circ_307868,RMVar_hsa_circ_143631 22058 RMVar_ID_22058 Human_SNP_ID_435203507 A-to-I Human chr10 - 63362221 63362217 63362221 ATTTTTTTTTTTTTTTTTAGAGATGCAGTCTCACTCTGTTGCGCGTGCTGGAGTGCAGTGTCATG ATTTTTTTTTTTTTTTTTAGAGATGCAGTCTC____TGTTGCGCGTGCTGGAGTGCAGTGTCATG AGAGT A JMJD1C Ensembl:ENSG00000171988 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs949211956 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_125595,RMVar_hsa_circ_307868,RMVar_hsa_circ_143631 22059 RMVar_ID_22059 Human_SNP_ID_435204258 A-to-I Human chr10 - 63364742 63364742 63364742 GTGAGGTGGCCTGTACTCCCAGCACTTAGGGAAGCTGAGGCAGGCAAATCACTTGAGTCCAAGAG GTGAGGTGGCCTGTACTCCCAGCACTTAGGGAGGCTGAGGCAGGCAAATCACTTGAGTCCAAGAG T C JMJD1C Ensembl:ENSG00000171988 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs761297645 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125595,RMVar_hsa_circ_307868,RMVar_hsa_circ_143631 22060 RMVar_ID_22060 Human_SNP_ID_435204419 A-to-I Human chr10 - 63365525 63365525 63365525 ACCTCGTGATCCACCTGCCTCAGCCTCCCAAAATGCTGAGATTACAGGCTTGAGCCACTGCACCT ACCTCGTGATCCACCTGCCTCAGCCTCCCAAAGTGCTGAGATTACAGGCTTGAGCCACTGCACCT T C JMJD1C Ensembl:ENSG00000171988 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1446673092 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125595,RMVar_hsa_circ_307868,RMVar_hsa_circ_143631 22061 RMVar_ID_22061 Human_SNP_ID_435204420 A-to-I Human chr10 - 63365525 63365525 63365525 ACCTCGTGATCCACCTGCCTCAGCCTCCCAAAATGCTGAGATTACAGGCTTGAGCCACTGCACCT ACCTCGTGATCCACCTGCCTCAGCCTCCCAAACTGCTGAGATTACAGGCTTGAGCCACTGCACCT T G JMJD1C Ensembl:ENSG00000171988 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1446673092 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125595,RMVar_hsa_circ_307868,RMVar_hsa_circ_143631 22062 RMVar_ID_22062 Human_SNP_ID_435206956 A-to-I Human chr10 - 63375643 63375643 63375643 GAGAGGCTAAGTCTGAAGGATTGCATAAGCCCAGGAGTTCATGGCTGCAGTGAGCCATGATTGTG GAGAGGCTAAGTCTGAAGGATTGCATAAGCCCGGGAGTTCATGGCTGCAGTGAGCCATGATTGTG T C JMJD1C Ensembl:ENSG00000171988 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1375136826 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2040003,Human_miRNA_ID_2553878,Human_miRNA_ID_3018984 RMVar_hsa_circ_125595,RMVar_hsa_circ_307868,RMVar_hsa_circ_143631 22063 RMVar_ID_22063 Human_SNP_ID_435208204 A-to-I Human chr10 - 63380147 63380147 63380147 TTGAAGCCAGGAGTTGGAGATCAGCCTGGGCAAAAAAGCGAGACCCCATCTCTACCAAAAAAAAA TTGAAGCCAGGAGTTGGAGATCAGCCTGGGCAGAAAAGCGAGACCCCATCTCTACCAAAAAAAAA T C JMJD1C Ensembl:ENSG00000171988 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs555603746 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125595,RMVar_hsa_circ_307868,RMVar_hsa_circ_143631 22064 RMVar_ID_22064 Human_SNP_ID_435217684 A-to-I Human chr10 - 63414125 63414125 63414125 AAAATTAGCTGGGCGTGTTGGCGGACACCTGCAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTAGCTGGGCGTGTTGGCGGACACCTGCTGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA T A JMJD1C Ensembl:ENSG00000171988 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1450400079 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_143636,RMVar_hsa_circ_143637 22065 RMVar_ID_22065 Human_SNP_ID_435227323 A-to-I Human chr10 - 63450030 63450030 63450030 CAGCTCATTGTAGCCCGGACCTCCTGGGCCCAAGTGAGCCTCCTATCTCAGCCTCCCAAGTTACT CAGCTCATTGTAGCCCGGACCTCCTGGGCCCAGGTGAGCCTCCTATCTCAGCCTCCCAAGTTACT T C JMJD1C Ensembl:ENSG00000171988 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1323530010 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_143636,RMVar_hsa_circ_143637 22066 RMVar_ID_22066 Human_SNP_ID_435229553 A-to-I Human chr10 - 63458320 63458320 63458320 CCATGCCTGGCTAATTTTTTTTTACTCTTTGTAGAGATGGAGTCTGACTGTGTTGCCCAGGCTGG CCATGCCTGGCTAATTTTTTTTTACTCTTTGTGGAGATGGAGTCTGACTGTGTTGCCCAGGCTGG T C JMJD1C Ensembl:ENSG00000171988 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1411785112 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11390472,Human_RBP_ID_24821381 RMVar_hsa_circ_143637 22067 RMVar_ID_22067 Human_SNP_ID_435246721 A-to-I Human chr10 + 63524927 63524927 63524927 CTGGCTACTAGGGAAGCTGAGGCACTAGAATCACTTGAACCCTGGAGGCAAAGGTTGCAGTGAGC CTGGCTACTAGGGAAGCTGAGGCACTAGAATCCCTTGAACCCTGGAGGCAAAGGTTGCAGTGAGC A C REEP3 Ensembl:ENSG00000165476 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs556829039 Functional Loss SNV dbSNP153 33..33 33 - - - 22068 RMVar_ID_22068 Human_SNP_ID_435246722 A-to-I Human chr10 + 63524927 63524927 63524927 CTGGCTACTAGGGAAGCTGAGGCACTAGAATCACTTGAACCCTGGAGGCAAAGGTTGCAGTGAGC CTGGCTACTAGGGAAGCTGAGGCACTAGAATCGCTTGAACCCTGGAGGCAAAGGTTGCAGTGAGC A G REEP3 Ensembl:ENSG00000165476 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs556829039 Functional Loss SNV dbSNP153 33..33 33 - - - 22069 RMVar_ID_22069 Human_SNP_ID_435801144 A-to-I Human chr10 - 65831104 65831104 65831104 TATTTTTAGTAGAAATGGGGTTTCACCTTGTTAGCCAGGATGGTCTCGATTTCCTGTCCCTCGTG TATTTTTAGTAGAAATGGGGTTTCACCTTGTTGGCCAGGATGGTCTCGATTTCCTGTCCCTCGTG T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1231608548 Functional Loss SNV dbSNP153 33..33 33 - - - 22070 RMVar_ID_22070 Human_SNP_ID_436107948 A-to-I Human chr10 + 67046666 67046666 67046666 GTAATTTCAGCAGAAAAGATTGGAAGCATGGTACTAGGGATACTATACATTGGCACAGGAGAAGA GTAATTTCAGCAGAAAAGATTGGAAGCATGGTGCTAGGGATACTATACATTGGCACAGGAGAAGA A G LRRTM3 Ensembl:ENSG00000198739 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1436898067 Functional Loss SNV dbSNP153 33..33 33 - - - 22071 RMVar_ID_22071 Human_SNP_ID_436111072 A-to-I Human chr10 + 67060197 67060197 67060197 AAAATTAGCTGGGTGTGATGACATGCGCCTGTAGTCTCAGCTACTTGGGAGGCTGAGATGGGAGG AAAATTAGCTGGGTGTGATGACATGCGCCTGTCGTCTCAGCTACTTGGGAGGCTGAGATGGGAGG A C LRRTM3 Ensembl:ENSG00000198739 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1463706744 Functional Loss SNV dbSNP153 33..33 33 - - - 22072 RMVar_ID_22072 Human_SNP_ID_436279192 A-to-I Human chr10 + 67751014 67751014 67751014 ATTAAGGAGATTGCTGCAAGGCACAAAAAACCACAGCCCAGGTTCTGATCCATTTCCATATCCAG ATTAAGGAGATTGCTGCAAGGCACAAAAAACCGCAGCCCAGGTTCTGATCCATTTCCATATCCAG A G AKR1B10P1 Ensembl:ENSG00000213606 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878998812 Functional Loss SNV dbSNP153 33..33 33 - - - 22073 RMVar_ID_22073 Human_SNP_ID_436279195 A-to-I Human chr10 + 67751033 67751033 67751033 GGCACAAAAAACCACAGCCCAGGTTCTGATCCATTTCCATATCCAGAGGAATGTGACTGTGATCC GGCACAAAAAACCACAGCCCAGGTTCTGATCCGTTTCCATATCCAGAGGAATGTGACTGTGATCC A G AKR1B10P1 Ensembl:ENSG00000213606 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878873859 Functional Loss SNV dbSNP153 33..33 33 - - - 22074 RMVar_ID_22074 Human_SNP_ID_436313280 A-to-I Human chr10 + 67886126 67886126 67886126 CACCACGCCCAGCTAATTTTTGTGTTTTTAGCAGAGACGGGGTTTCACCATGTTGGCCAGGATGG CACCACGCCCAGCTAATTTTTGTGTTTTTAGCGGAGACGGGGTTTCACCATGTTGGCCAGGATGG A G SIRT1 Ensembl:ENSG00000096717 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs548619000 Functional Loss SNV dbSNP153 33..33 33 - - - 22075 RMVar_ID_22075 Human_SNP_ID_436315988 A-to-I Human chr10 + 67894784 67894784 67894784 CAGGCTGTAGTGCATTGGCGCGATCTCGGCTCACTGCATCCTCCACCTCCCGGGTTCAAGCAATT CAGGCTGTAGTGCATTGGCGCGATCTCGGCTCCCTGCATCCTCCACCTCCCGGGTTCAAGCAATT A C SIRT1 Ensembl:ENSG00000096717 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs576886247 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_306350,RMVar_hsa_circ_312270,RMVar_hsa_circ_344218,RMVar_hsa_circ_305621,RMVar_hsa_circ_308242,RMVar_hsa_circ_324620,RMVar_hsa_circ_298084,RMVar_hsa_circ_341213,RMVar_hsa_circ_314097 22076 RMVar_ID_22076 Human_SNP_ID_436315989 A-to-I Human chr10 + 67894784 67894784 67894784 CAGGCTGTAGTGCATTGGCGCGATCTCGGCTCACTGCATCCTCCACCTCCCGGGTTCAAGCAATT CAGGCTGTAGTGCATTGGCGCGATCTCGGCTCGCTGCATCCTCCACCTCCCGGGTTCAAGCAATT A G SIRT1 Ensembl:ENSG00000096717 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs576886247 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_306350,RMVar_hsa_circ_312270,RMVar_hsa_circ_344218,RMVar_hsa_circ_305621,RMVar_hsa_circ_308242,RMVar_hsa_circ_324620,RMVar_hsa_circ_298084,RMVar_hsa_circ_341213,RMVar_hsa_circ_314097 22077 RMVar_ID_22077 Human_SNP_ID_436316055 A-to-I Human chr10 + 67894957 67894957 67894957 TGACCTCGTGATCCGCCCGTTTCAGCCTCCCAAAGTGTTGGGATTACAGGTGTGAGCCACAATGT TGACCTCGTGATCCGCCCGTTTCAGCCTCCCAGAGTGTTGGGATTACAGGTGTGAGCCACAATGT A G SIRT1 Ensembl:ENSG00000096717 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs940495215 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_306350,RMVar_hsa_circ_312270,RMVar_hsa_circ_344218,RMVar_hsa_circ_305621,RMVar_hsa_circ_308242,RMVar_hsa_circ_324620,RMVar_hsa_circ_298084,RMVar_hsa_circ_341213,RMVar_hsa_circ_314097 22078 RMVar_ID_22078 Human_SNP_ID_436316056 A-to-I Human chr10 + 67894957 67894957 67894957 TGACCTCGTGATCCGCCCGTTTCAGCCTCCCAAAGTGTTGGGATTACAGGTGTGAGCCACAATGT TGACCTCGTGATCCGCCCGTTTCAGCCTCCCATAGTGTTGGGATTACAGGTGTGAGCCACAATGT A T SIRT1 Ensembl:ENSG00000096717 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs940495215 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_306350,RMVar_hsa_circ_312270,RMVar_hsa_circ_344218,RMVar_hsa_circ_305621,RMVar_hsa_circ_308242,RMVar_hsa_circ_324620,RMVar_hsa_circ_298084,RMVar_hsa_circ_341213,RMVar_hsa_circ_314097 22079 RMVar_ID_22079 Human_SNP_ID_436316397 A-to-I Human chr10 + 67895816 67895816 67895816 CAGGCTGGAGTGCCGTGGTGAGATCTCGGCTCACTACAACCTTCACCTCCCGAGTTCAAGCAATT CAGGCTGGAGTGCCGTGGTGAGATCTCGGCTCGCTACAACCTTCACCTCCCGAGTTCAAGCAATT A G SIRT1 Ensembl:ENSG00000096717 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs762141565 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_306350,RMVar_hsa_circ_312270,RMVar_hsa_circ_344218,RMVar_hsa_circ_305621,RMVar_hsa_circ_308242,RMVar_hsa_circ_324620,RMVar_hsa_circ_298084,RMVar_hsa_circ_341213,RMVar_hsa_circ_314097 22080 RMVar_ID_22080 Human_SNP_ID_436316889 A-to-I Human chr10 + 67897566 67897566 67897566 TTGTATTTTTAGTAGAGACGGGGTTTCACCATATTGGCCAGGCTGGTCTCGAACTCTTGACCTTG TTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCTTGACCTTG A G SIRT1 Ensembl:ENSG00000096717 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs929893065 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_306350,RMVar_hsa_circ_312270,RMVar_hsa_circ_344218,RMVar_hsa_circ_305621,RMVar_hsa_circ_308242,RMVar_hsa_circ_324620,RMVar_hsa_circ_298084,RMVar_hsa_circ_341213,RMVar_hsa_circ_314097 22081 RMVar_ID_22081 Human_SNP_ID_436317636 A-to-I Human chr10 + 67900068 67900068 67900068 AATATGCTGCTGTACTCCAGCCTGGGCAACAGAGCGAGACTCTATCTCAAAAATAAATACAATTT AATATGCTGCTGTACTCCAGCCTGGGCAACAGGGCGAGACTCTATCTCAAAAATAAATACAATTT A G SIRT1 Ensembl:ENSG00000096717 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1451522257 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_306350,RMVar_hsa_circ_312270,RMVar_hsa_circ_344218,RMVar_hsa_circ_305621,RMVar_hsa_circ_308242,RMVar_hsa_circ_324620,RMVar_hsa_circ_298084,RMVar_hsa_circ_341213,RMVar_hsa_circ_314097 22082 RMVar_ID_22082 Human_SNP_ID_436318930 A-to-I Human chr10 + 67904267 67904267 67904267 CTCCCACCTCAGCCTTCTGAGTTTCTGGGACTACAGGCATGAACCGTGAGGCCCAGCTAATTTTT CTCCCACCTCAGCCTTCTGAGTTTCTGGGACTGCAGGCATGAACCGTGAGGCCCAGCTAATTTTT A G SIRT1 Ensembl:ENSG00000096717 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs564666153 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_306350,RMVar_hsa_circ_312270,RMVar_hsa_circ_344218,RMVar_hsa_circ_305621,RMVar_hsa_circ_308242,RMVar_hsa_circ_324620,RMVar_hsa_circ_298084,RMVar_hsa_circ_341213,RMVar_hsa_circ_314097 22083 RMVar_ID_22083 Human_SNP_ID_436330936 A-to-I Human chr10 - 67949863 67949863 67949863 AGGTGTGCGCCACCATACCTGGCTAGTTTTTTATATTGTTGGTAGAGACGAGGTTTCACCATGTT AGGTGTGCGCCACCATACCTGGCTAGTTTTTTGTATTGTTGGTAGAGACGAGGTTTCACCATGTT T C HERC4 Ensembl:ENSG00000148634 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1033099565 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11393189 RMVar_hsa_circ_11263,RMVar_hsa_circ_10657,RMVar_hsa_circ_125199,RMVar_hsa_circ_58582,RMVar_hsa_circ_63493,RMVar_hsa_circ_292715,RMVar_hsa_circ_321221,RMVar_hsa_circ_143661,RMVar_hsa_circ_297679,RMVar_hsa_circ_275538,RMVar_hsa_circ_292297,RMVar_hsa_circ_97971,RMVar_hsa_circ_24480,RMVar_hsa_circ_19756,RMVar_hsa_circ_59326,RMVar_hsa_circ_56329,RMVar_hsa_circ_143663,RMVar_hsa_circ_143665,RMVar_hsa_circ_143666,RMVar_hsa_circ_143664,RMVar_hsa_circ_143662,RMVar_hsa_circ_16163,RMVar_hsa_circ_36680,RMVar_hsa_circ_310441,RMVar_hsa_circ_341088,RMVar_hsa_circ_67231,RMVar_hsa_circ_80660,RMVar_hsa_circ_308585,RMVar_hsa_circ_320909,RMVar_hsa_circ_333423,RMVar_hsa_circ_264986,RMVar_hsa_circ_143670,RMVar_hsa_circ_143672,RMVar_hsa_circ_46847,RMVar_hsa_circ_143671 22084 RMVar_ID_22084 Human_SNP_ID_436331587 A-to-I Human chr10 - 67952864 67952864 67952864 ACTGAGTCTCCCTCTGTCGCCCAGGCTGGAGTACAGTGGCGCACTCTCGGCTCACTGCAAGCTCT ACTGAGTCTCCCTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCACTCTCGGCTCACTGCAAGCTCT T C HERC4 Ensembl:ENSG00000148634 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1038779312 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11263,RMVar_hsa_circ_10657,RMVar_hsa_circ_125199,RMVar_hsa_circ_58582,RMVar_hsa_circ_63493,RMVar_hsa_circ_292715,RMVar_hsa_circ_321221,RMVar_hsa_circ_143661,RMVar_hsa_circ_297679,RMVar_hsa_circ_275538,RMVar_hsa_circ_292297,RMVar_hsa_circ_97971,RMVar_hsa_circ_24480,RMVar_hsa_circ_19756,RMVar_hsa_circ_59326,RMVar_hsa_circ_56329,RMVar_hsa_circ_143663,RMVar_hsa_circ_143665,RMVar_hsa_circ_143666,RMVar_hsa_circ_143664,RMVar_hsa_circ_143662,RMVar_hsa_circ_16163,RMVar_hsa_circ_36680,RMVar_hsa_circ_310441,RMVar_hsa_circ_341088,RMVar_hsa_circ_67231,RMVar_hsa_circ_80660,RMVar_hsa_circ_308585,RMVar_hsa_circ_320909,RMVar_hsa_circ_333423,RMVar_hsa_circ_264986,RMVar_hsa_circ_143670,RMVar_hsa_circ_143672,RMVar_hsa_circ_46847,RMVar_hsa_circ_143671 22085 RMVar_ID_22085 Human_SNP_ID_436331729 A-to-I Human chr10 + 67953478 67953478 67953478 ATAAGTCTGGAACATTCTGTCATAGTAAGTACACAAGGTAGCAAGGAAGGTACCAAAAAGTATAT ATAAGTCTGGAACATTCTGTCATAGTAAGTACGCAAGGTAGCAAGGAAGGTACCAAAAAGTATAT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs553438438 Functional Loss SNV dbSNP153 33..33 33 - - - 22086 RMVar_ID_22086 Human_SNP_ID_436337888 A-to-I Human chr10 - 67980271 67980271 67980271 AAATTAGCCAGGCATGGTGGCGCATGTCTGTAATCCCAGCTACTTGGGAGGCTGAGACAGGAGAA AAATTAGCCAGGCATGGTGGCGCATGTCTGTAGTCCCAGCTACTTGGGAGGCTGAGACAGGAGAA T C HERC4 Ensembl:ENSG00000148634 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264402300 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11263,RMVar_hsa_circ_10657,RMVar_hsa_circ_125199,RMVar_hsa_circ_63493,RMVar_hsa_circ_321221,RMVar_hsa_circ_143661,RMVar_hsa_circ_297679,RMVar_hsa_circ_275538,RMVar_hsa_circ_97971,RMVar_hsa_circ_24480,RMVar_hsa_circ_108552,RMVar_hsa_circ_59326,RMVar_hsa_circ_56329,RMVar_hsa_circ_143663,RMVar_hsa_circ_143664,RMVar_hsa_circ_143662,RMVar_hsa_circ_16163,RMVar_hsa_circ_36680,RMVar_hsa_circ_310441,RMVar_hsa_circ_80660,RMVar_hsa_circ_308585,RMVar_hsa_circ_264986,RMVar_hsa_circ_113391,RMVar_hsa_circ_309776,RMVar_hsa_circ_143672,RMVar_hsa_circ_143671,RMVar_hsa_circ_353674,RMVar_hsa_circ_320283,RMVar_hsa_circ_312802,RMVar_hsa_circ_288160,RMVar_hsa_circ_277400,RMVar_hsa_circ_35207,RMVar_hsa_circ_58500,RMVar_hsa_circ_73971,RMVar_hsa_circ_42799,RMVar_hsa_circ_143675,RMVar_hsa_circ_143677,RMVar_hsa_circ_143679,RMVar_hsa_circ_143678,RMVar_hsa_circ_143676,RMVar_hsa_circ_143673,RMVar_hsa_circ_143674,RMVar_hsa_circ_364295,RMVar_hsa_circ_143687,RMVar_hsa_circ_72423,RMVar_hsa_circ_7505,RMVar_hsa_circ_29076,RMVar_hsa_circ_143682,RMVar_hsa_circ_291844,RMVar_hsa_circ_318323,RMVar_hsa_circ_372966,RMVar_hsa_circ_143683,RMVar_hsa_circ_331700,RMVar_hsa_circ_293289,RMVar_hsa_circ_280977,RMVar_hsa_circ_291328,RMVar_hsa_circ_273519,RMVar_hsa_circ_143689,RMVar_hsa_circ_143691,RMVar_hsa_circ_143693,RMVar_hsa_circ_42778,RMVar_hsa_circ_143692,RMVar_hsa_circ_143690,RMVar_hsa_circ_143688,RMVar_hsa_circ_143685,RMVar_hsa_circ_143686,RMVar_hsa_circ_143684 22087 RMVar_ID_22087 Human_SNP_ID_436339012 A-to-I Human chr10 - 67984711 67984711 67984711 GAGCGTGGTGGCACGTGTCTGTAATACCAACTATTCAGAAGGCTGAGGCAGGAGAATTGCTTGAA GAGCGTGGTGGCACGTGTCTGTAATACCAACTGTTCAGAAGGCTGAGGCAGGAGAATTGCTTGAA T C HERC4 Ensembl:ENSG00000148634 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1039113312 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11263,RMVar_hsa_circ_10657,RMVar_hsa_circ_125199,RMVar_hsa_circ_63493,RMVar_hsa_circ_321221,RMVar_hsa_circ_143661,RMVar_hsa_circ_297679,RMVar_hsa_circ_275538,RMVar_hsa_circ_97971,RMVar_hsa_circ_24480,RMVar_hsa_circ_108552,RMVar_hsa_circ_59326,RMVar_hsa_circ_56329,RMVar_hsa_circ_143663,RMVar_hsa_circ_143664,RMVar_hsa_circ_143662,RMVar_hsa_circ_16163,RMVar_hsa_circ_36680,RMVar_hsa_circ_310441,RMVar_hsa_circ_80660,RMVar_hsa_circ_308585,RMVar_hsa_circ_264986,RMVar_hsa_circ_113391,RMVar_hsa_circ_309776,RMVar_hsa_circ_143672,RMVar_hsa_circ_143671,RMVar_hsa_circ_353674,RMVar_hsa_circ_320283,RMVar_hsa_circ_312802,RMVar_hsa_circ_288160,RMVar_hsa_circ_277400,RMVar_hsa_circ_35207,RMVar_hsa_circ_58500,RMVar_hsa_circ_73971,RMVar_hsa_circ_42799,RMVar_hsa_circ_143675,RMVar_hsa_circ_143677,RMVar_hsa_circ_143679,RMVar_hsa_circ_143678,RMVar_hsa_circ_143676,RMVar_hsa_circ_143673,RMVar_hsa_circ_143674,RMVar_hsa_circ_364295,RMVar_hsa_circ_143687,RMVar_hsa_circ_72423,RMVar_hsa_circ_7505,RMVar_hsa_circ_29076,RMVar_hsa_circ_143682,RMVar_hsa_circ_291844,RMVar_hsa_circ_318323,RMVar_hsa_circ_372966,RMVar_hsa_circ_143683,RMVar_hsa_circ_331700,RMVar_hsa_circ_293289,RMVar_hsa_circ_280977,RMVar_hsa_circ_291328,RMVar_hsa_circ_273519,RMVar_hsa_circ_143689,RMVar_hsa_circ_143691,RMVar_hsa_circ_143693,RMVar_hsa_circ_42778,RMVar_hsa_circ_143692,RMVar_hsa_circ_143690,RMVar_hsa_circ_143688,RMVar_hsa_circ_143685,RMVar_hsa_circ_143686,RMVar_hsa_circ_143684 22088 RMVar_ID_22088 Human_SNP_ID_436339013 A-to-I Human chr10 - 67984711 67984711 67984711 GAGCGTGGTGGCACGTGTCTGTAATACCAACTATTCAGAAGGCTGAGGCAGGAGAATTGCTTGAA GAGCGTGGTGGCACGTGTCTGTAATACCAACTCTTCAGAAGGCTGAGGCAGGAGAATTGCTTGAA T G HERC4 Ensembl:ENSG00000148634 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1039113312 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11263,RMVar_hsa_circ_10657,RMVar_hsa_circ_125199,RMVar_hsa_circ_63493,RMVar_hsa_circ_321221,RMVar_hsa_circ_143661,RMVar_hsa_circ_297679,RMVar_hsa_circ_275538,RMVar_hsa_circ_97971,RMVar_hsa_circ_24480,RMVar_hsa_circ_108552,RMVar_hsa_circ_59326,RMVar_hsa_circ_56329,RMVar_hsa_circ_143663,RMVar_hsa_circ_143664,RMVar_hsa_circ_143662,RMVar_hsa_circ_16163,RMVar_hsa_circ_36680,RMVar_hsa_circ_310441,RMVar_hsa_circ_80660,RMVar_hsa_circ_308585,RMVar_hsa_circ_264986,RMVar_hsa_circ_113391,RMVar_hsa_circ_309776,RMVar_hsa_circ_143672,RMVar_hsa_circ_143671,RMVar_hsa_circ_353674,RMVar_hsa_circ_320283,RMVar_hsa_circ_312802,RMVar_hsa_circ_288160,RMVar_hsa_circ_277400,RMVar_hsa_circ_35207,RMVar_hsa_circ_58500,RMVar_hsa_circ_73971,RMVar_hsa_circ_42799,RMVar_hsa_circ_143675,RMVar_hsa_circ_143677,RMVar_hsa_circ_143679,RMVar_hsa_circ_143678,RMVar_hsa_circ_143676,RMVar_hsa_circ_143673,RMVar_hsa_circ_143674,RMVar_hsa_circ_364295,RMVar_hsa_circ_143687,RMVar_hsa_circ_72423,RMVar_hsa_circ_7505,RMVar_hsa_circ_29076,RMVar_hsa_circ_143682,RMVar_hsa_circ_291844,RMVar_hsa_circ_318323,RMVar_hsa_circ_372966,RMVar_hsa_circ_143683,RMVar_hsa_circ_331700,RMVar_hsa_circ_293289,RMVar_hsa_circ_280977,RMVar_hsa_circ_291328,RMVar_hsa_circ_273519,RMVar_hsa_circ_143689,RMVar_hsa_circ_143691,RMVar_hsa_circ_143693,RMVar_hsa_circ_42778,RMVar_hsa_circ_143692,RMVar_hsa_circ_143690,RMVar_hsa_circ_143688,RMVar_hsa_circ_143685,RMVar_hsa_circ_143686,RMVar_hsa_circ_143684 22089 RMVar_ID_22089 Human_SNP_ID_436341812 A-to-I Human chr10 - 67996866 67996866 67996866 CTCCTGCCTCAGCCTCCCAAGTAGCCGGGACTACAGGCACCTGCCGCCACGCCCAGCTAATTTTT CTCCTGCCTCAGCCTCCCAAGTAGCCGGGACTGCAGGCACCTGCCGCCACGCCCAGCTAATTTTT T C HERC4 Ensembl:ENSG00000148634 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1204065286 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11263,RMVar_hsa_circ_125199,RMVar_hsa_circ_321221,RMVar_hsa_circ_143661,RMVar_hsa_circ_297679,RMVar_hsa_circ_275538,RMVar_hsa_circ_97971,RMVar_hsa_circ_108552,RMVar_hsa_circ_59326,RMVar_hsa_circ_56329,RMVar_hsa_circ_143663,RMVar_hsa_circ_143662,RMVar_hsa_circ_16163,RMVar_hsa_circ_310441,RMVar_hsa_circ_80660,RMVar_hsa_circ_113391,RMVar_hsa_circ_143672,RMVar_hsa_circ_320283,RMVar_hsa_circ_312802,RMVar_hsa_circ_288160,RMVar_hsa_circ_277400,RMVar_hsa_circ_35207,RMVar_hsa_circ_58500,RMVar_hsa_circ_73971,RMVar_hsa_circ_143675,RMVar_hsa_circ_143677,RMVar_hsa_circ_143678,RMVar_hsa_circ_143676,RMVar_hsa_circ_143673,RMVar_hsa_circ_143674,RMVar_hsa_circ_364295,RMVar_hsa_circ_143687,RMVar_hsa_circ_72423,RMVar_hsa_circ_7505,RMVar_hsa_circ_143682,RMVar_hsa_circ_291844,RMVar_hsa_circ_318323,RMVar_hsa_circ_372966,RMVar_hsa_circ_143683,RMVar_hsa_circ_293289,RMVar_hsa_circ_280977,RMVar_hsa_circ_273519,RMVar_hsa_circ_143689,RMVar_hsa_circ_143691,RMVar_hsa_circ_143690,RMVar_hsa_circ_143688,RMVar_hsa_circ_143700,RMVar_hsa_circ_45978,RMVar_hsa_circ_143685,RMVar_hsa_circ_143686,RMVar_hsa_circ_282075,RMVar_hsa_circ_143684,RMVar_hsa_circ_277438,RMVar_hsa_circ_302373,RMVar_hsa_circ_143694,RMVar_hsa_circ_143695,RMVar_hsa_circ_365501,RMVar_hsa_circ_334670,RMVar_hsa_circ_344718,RMVar_hsa_circ_49276,RMVar_hsa_circ_279414,RMVar_hsa_circ_143701,RMVar_hsa_circ_143702,RMVar_hsa_circ_143698,RMVar_hsa_circ_143699,RMVar_hsa_circ_143697,RMVar_hsa_circ_27343,RMVar_hsa_circ_315590,RMVar_hsa_circ_72407,RMVar_hsa_circ_281570,RMVar_hsa_circ_294561,RMVar_hsa_circ_294472,RMVar_hsa_circ_50936,RMVar_hsa_circ_277371,RMVar_hsa_circ_143703,RMVar_hsa_circ_143704,RMVar_hsa_circ_143705,RMVar_hsa_circ_304522,RMVar_hsa_circ_317897,RMVar_hsa_circ_321834,RMVar_hsa_circ_143708,RMVar_hsa_circ_143709,RMVar_hsa_circ_143707,RMVar_hsa_circ_34458,RMVar_hsa_circ_50317 22090 RMVar_ID_22090 Human_SNP_ID_436344715 A-to-I Human chr10 - 68008964 68008964 68008964 TGCCCACCTTGGCCTCTTAAAGTGCTGGGATTACAGGAGTGAACCACTGCGCCCAGGCTAGTATA TGCCCACCTTGGCCTCTTAAAGTGCTGGGATTGCAGGAGTGAACCACTGCGCCCAGGCTAGTATA T C HERC4 Ensembl:ENSG00000148634 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs778516639 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11263,RMVar_hsa_circ_125199,RMVar_hsa_circ_321221,RMVar_hsa_circ_143661,RMVar_hsa_circ_297679,RMVar_hsa_circ_275538,RMVar_hsa_circ_97971,RMVar_hsa_circ_108552,RMVar_hsa_circ_59326,RMVar_hsa_circ_56329,RMVar_hsa_circ_143663,RMVar_hsa_circ_143662,RMVar_hsa_circ_16163,RMVar_hsa_circ_310441,RMVar_hsa_circ_80660,RMVar_hsa_circ_113391,RMVar_hsa_circ_143672,RMVar_hsa_circ_320283,RMVar_hsa_circ_312802,RMVar_hsa_circ_288160,RMVar_hsa_circ_277400,RMVar_hsa_circ_35207,RMVar_hsa_circ_58500,RMVar_hsa_circ_73971,RMVar_hsa_circ_143675,RMVar_hsa_circ_143677,RMVar_hsa_circ_143678,RMVar_hsa_circ_143676,RMVar_hsa_circ_143673,RMVar_hsa_circ_143674,RMVar_hsa_circ_364295,RMVar_hsa_circ_143687,RMVar_hsa_circ_72423,RMVar_hsa_circ_7505,RMVar_hsa_circ_143682,RMVar_hsa_circ_291844,RMVar_hsa_circ_318323,RMVar_hsa_circ_372966,RMVar_hsa_circ_143683,RMVar_hsa_circ_293289,RMVar_hsa_circ_280977,RMVar_hsa_circ_273519,RMVar_hsa_circ_143689,RMVar_hsa_circ_143691,RMVar_hsa_circ_143690,RMVar_hsa_circ_143688,RMVar_hsa_circ_143700,RMVar_hsa_circ_45978,RMVar_hsa_circ_143685,RMVar_hsa_circ_143686,RMVar_hsa_circ_282075,RMVar_hsa_circ_143684,RMVar_hsa_circ_277438,RMVar_hsa_circ_302373,RMVar_hsa_circ_143694,RMVar_hsa_circ_143695,RMVar_hsa_circ_365501,RMVar_hsa_circ_334670,RMVar_hsa_circ_344718,RMVar_hsa_circ_49276,RMVar_hsa_circ_279414,RMVar_hsa_circ_143701,RMVar_hsa_circ_143702,RMVar_hsa_circ_143698,RMVar_hsa_circ_143699,RMVar_hsa_circ_143697,RMVar_hsa_circ_27343,RMVar_hsa_circ_315590,RMVar_hsa_circ_72407,RMVar_hsa_circ_281570,RMVar_hsa_circ_294561,RMVar_hsa_circ_294472,RMVar_hsa_circ_50936,RMVar_hsa_circ_277371,RMVar_hsa_circ_143703,RMVar_hsa_circ_143704,RMVar_hsa_circ_143705,RMVar_hsa_circ_304522,RMVar_hsa_circ_317897,RMVar_hsa_circ_321834,RMVar_hsa_circ_143708,RMVar_hsa_circ_143709,RMVar_hsa_circ_143707,RMVar_hsa_circ_34458,RMVar_hsa_circ_50317 22091 RMVar_ID_22091 Human_SNP_ID_436348698 A-to-I Human chr10 - 68026260 68026260 68026260 AAAACCCCATCTCTACAAAAAAGTAAAAAATTAGCCAGATGTGGTGGTGCATGCCTGCACTCCCA AAAACCCCATCTCTACAAAAAAGTAAAAAATTTGCCAGATGTGGTGGTGCATGCCTGCACTCCCA T A HERC4 Ensembl:ENSG00000148634 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs189549197 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11394036 RMVar_hsa_circ_125199,RMVar_hsa_circ_143661,RMVar_hsa_circ_297679,RMVar_hsa_circ_275538,RMVar_hsa_circ_97971,RMVar_hsa_circ_108552,RMVar_hsa_circ_59326,RMVar_hsa_circ_143662,RMVar_hsa_circ_80660,RMVar_hsa_circ_113391,RMVar_hsa_circ_143672,RMVar_hsa_circ_320283,RMVar_hsa_circ_312802,RMVar_hsa_circ_277400,RMVar_hsa_circ_58500,RMVar_hsa_circ_73971,RMVar_hsa_circ_143675,RMVar_hsa_circ_143676,RMVar_hsa_circ_143673,RMVar_hsa_circ_143674,RMVar_hsa_circ_143687,RMVar_hsa_circ_72423,RMVar_hsa_circ_143682,RMVar_hsa_circ_318323,RMVar_hsa_circ_372966,RMVar_hsa_circ_280977,RMVar_hsa_circ_273519,RMVar_hsa_circ_143688,RMVar_hsa_circ_143700,RMVar_hsa_circ_45978,RMVar_hsa_circ_143685,RMVar_hsa_circ_143686,RMVar_hsa_circ_282075,RMVar_hsa_circ_143684,RMVar_hsa_circ_143695,RMVar_hsa_circ_334670,RMVar_hsa_circ_344718,RMVar_hsa_circ_49276,RMVar_hsa_circ_279414,RMVar_hsa_circ_143701,RMVar_hsa_circ_143702,RMVar_hsa_circ_143699,RMVar_hsa_circ_27343,RMVar_hsa_circ_315590,RMVar_hsa_circ_72407,RMVar_hsa_circ_294561,RMVar_hsa_circ_294472,RMVar_hsa_circ_50936,RMVar_hsa_circ_19229,RMVar_hsa_circ_143703,RMVar_hsa_circ_143704,RMVar_hsa_circ_317897,RMVar_hsa_circ_321834,RMVar_hsa_circ_143709,RMVar_hsa_circ_143711,RMVar_hsa_circ_319556,RMVar_hsa_circ_34458,RMVar_hsa_circ_50317,RMVar_hsa_circ_341745,RMVar_hsa_circ_365812,RMVar_hsa_circ_271218,RMVar_hsa_circ_279810,RMVar_hsa_circ_20291,RMVar_hsa_circ_113913,RMVar_hsa_circ_311037,RMVar_hsa_circ_378339,RMVar_hsa_circ_143710,RMVar_hsa_circ_346845,RMVar_hsa_circ_272171,RMVar_hsa_circ_143714,RMVar_hsa_circ_3277,RMVar_hsa_circ_143715,RMVar_hsa_circ_143713 22092 RMVar_ID_22092 Human_SNP_ID_436349418 A-to-I Human chr10 - 68029328 68029328 68029328 ATCACCACACCTGGCTAATTTTCTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTAGCCAGGC ATCACCACACCTGGCTAATTTTCTGTATTTTTGGTAGAGATGGGGTTTCACCATGTTAGCCAGGC T C HERC4 Ensembl:ENSG00000148634 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1409770857 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125199,RMVar_hsa_circ_143661,RMVar_hsa_circ_297679,RMVar_hsa_circ_275538,RMVar_hsa_circ_97971,RMVar_hsa_circ_108552,RMVar_hsa_circ_59326,RMVar_hsa_circ_143662,RMVar_hsa_circ_80660,RMVar_hsa_circ_113391,RMVar_hsa_circ_143672,RMVar_hsa_circ_320283,RMVar_hsa_circ_312802,RMVar_hsa_circ_277400,RMVar_hsa_circ_58500,RMVar_hsa_circ_73971,RMVar_hsa_circ_143675,RMVar_hsa_circ_143676,RMVar_hsa_circ_143673,RMVar_hsa_circ_143674,RMVar_hsa_circ_143687,RMVar_hsa_circ_72423,RMVar_hsa_circ_143682,RMVar_hsa_circ_318323,RMVar_hsa_circ_372966,RMVar_hsa_circ_280977,RMVar_hsa_circ_273519,RMVar_hsa_circ_143688,RMVar_hsa_circ_143700,RMVar_hsa_circ_45978,RMVar_hsa_circ_143685,RMVar_hsa_circ_143686,RMVar_hsa_circ_282075,RMVar_hsa_circ_143684,RMVar_hsa_circ_143695,RMVar_hsa_circ_334670,RMVar_hsa_circ_344718,RMVar_hsa_circ_49276,RMVar_hsa_circ_279414,RMVar_hsa_circ_143701,RMVar_hsa_circ_143702,RMVar_hsa_circ_143699,RMVar_hsa_circ_27343,RMVar_hsa_circ_315590,RMVar_hsa_circ_72407,RMVar_hsa_circ_294561,RMVar_hsa_circ_294472,RMVar_hsa_circ_50936,RMVar_hsa_circ_19229,RMVar_hsa_circ_143703,RMVar_hsa_circ_143704,RMVar_hsa_circ_317897,RMVar_hsa_circ_321834,RMVar_hsa_circ_143709,RMVar_hsa_circ_143711,RMVar_hsa_circ_319556,RMVar_hsa_circ_34458,RMVar_hsa_circ_50317,RMVar_hsa_circ_341745,RMVar_hsa_circ_365812,RMVar_hsa_circ_271218,RMVar_hsa_circ_279810,RMVar_hsa_circ_20291,RMVar_hsa_circ_113913,RMVar_hsa_circ_311037,RMVar_hsa_circ_378339,RMVar_hsa_circ_143710,RMVar_hsa_circ_346845,RMVar_hsa_circ_272171,RMVar_hsa_circ_143714,RMVar_hsa_circ_3277,RMVar_hsa_circ_143715,RMVar_hsa_circ_143713 22093 RMVar_ID_22093 Human_SNP_ID_436350046 A-to-I Human chr10 - 68031925 68031925 68031925 CAACTTGGTGAAACTCTGTCTCTTCTAAAAATACGAAAGTTAGCTGGGCATGGCGGCAGGCACCT CAACTTGGTGAAACTCTGTCTCTTCTAAAAATGCGAAAGTTAGCTGGGCATGGCGGCAGGCACCT T C HERC4 Ensembl:ENSG00000148634 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1308575628 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11394121 RMVar_hsa_circ_125199,RMVar_hsa_circ_143661,RMVar_hsa_circ_297679,RMVar_hsa_circ_275538,RMVar_hsa_circ_97971,RMVar_hsa_circ_108552,RMVar_hsa_circ_59326,RMVar_hsa_circ_143662,RMVar_hsa_circ_80660,RMVar_hsa_circ_113391,RMVar_hsa_circ_143672,RMVar_hsa_circ_320283,RMVar_hsa_circ_312802,RMVar_hsa_circ_277400,RMVar_hsa_circ_58500,RMVar_hsa_circ_73971,RMVar_hsa_circ_143675,RMVar_hsa_circ_143676,RMVar_hsa_circ_143673,RMVar_hsa_circ_143674,RMVar_hsa_circ_143687,RMVar_hsa_circ_72423,RMVar_hsa_circ_143682,RMVar_hsa_circ_318323,RMVar_hsa_circ_372966,RMVar_hsa_circ_280977,RMVar_hsa_circ_273519,RMVar_hsa_circ_143688,RMVar_hsa_circ_143700,RMVar_hsa_circ_45978,RMVar_hsa_circ_143685,RMVar_hsa_circ_143686,RMVar_hsa_circ_282075,RMVar_hsa_circ_143684,RMVar_hsa_circ_143695,RMVar_hsa_circ_334670,RMVar_hsa_circ_344718,RMVar_hsa_circ_49276,RMVar_hsa_circ_279414,RMVar_hsa_circ_143701,RMVar_hsa_circ_143702,RMVar_hsa_circ_143699,RMVar_hsa_circ_27343,RMVar_hsa_circ_315590,RMVar_hsa_circ_72407,RMVar_hsa_circ_294561,RMVar_hsa_circ_294472,RMVar_hsa_circ_50936,RMVar_hsa_circ_19229,RMVar_hsa_circ_143703,RMVar_hsa_circ_143704,RMVar_hsa_circ_317897,RMVar_hsa_circ_321834,RMVar_hsa_circ_143709,RMVar_hsa_circ_143711,RMVar_hsa_circ_319556,RMVar_hsa_circ_34458,RMVar_hsa_circ_50317,RMVar_hsa_circ_341745,RMVar_hsa_circ_365812,RMVar_hsa_circ_271218,RMVar_hsa_circ_279810,RMVar_hsa_circ_20291,RMVar_hsa_circ_113913,RMVar_hsa_circ_311037,RMVar_hsa_circ_378339,RMVar_hsa_circ_143710,RMVar_hsa_circ_346845,RMVar_hsa_circ_272171,RMVar_hsa_circ_143714,RMVar_hsa_circ_3277,RMVar_hsa_circ_143715,RMVar_hsa_circ_143713 22094 RMVar_ID_22094 Human_SNP_ID_436350817 A-to-I Human chr10 - 68035442 68035442 68035442 GGTAAGAGCGATTGTCCCAGGCTGGGTGTGGTAACTCACACCTGTAATCTTAGCACTTTGGGAGG GGTAAGAGCGATTGTCCCAGGCTGGGTGTGGTGACTCACACCTGTAATCTTAGCACTTTGGGAGG T C HERC4 Ensembl:ENSG00000148634 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984495010 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125199,RMVar_hsa_circ_143661,RMVar_hsa_circ_297679,RMVar_hsa_circ_275538,RMVar_hsa_circ_97971,RMVar_hsa_circ_108552,RMVar_hsa_circ_59326,RMVar_hsa_circ_143662,RMVar_hsa_circ_80660,RMVar_hsa_circ_143672,RMVar_hsa_circ_320283,RMVar_hsa_circ_312802,RMVar_hsa_circ_277400,RMVar_hsa_circ_58500,RMVar_hsa_circ_143675,RMVar_hsa_circ_143673,RMVar_hsa_circ_143674,RMVar_hsa_circ_143687,RMVar_hsa_circ_72423,RMVar_hsa_circ_143682,RMVar_hsa_circ_372966,RMVar_hsa_circ_280977,RMVar_hsa_circ_273519,RMVar_hsa_circ_143700,RMVar_hsa_circ_45978,RMVar_hsa_circ_143685,RMVar_hsa_circ_143686,RMVar_hsa_circ_282075,RMVar_hsa_circ_143684,RMVar_hsa_circ_143695,RMVar_hsa_circ_334670,RMVar_hsa_circ_344718,RMVar_hsa_circ_279414,RMVar_hsa_circ_143701,RMVar_hsa_circ_143702,RMVar_hsa_circ_143699,RMVar_hsa_circ_27343,RMVar_hsa_circ_315590,RMVar_hsa_circ_72407,RMVar_hsa_circ_294561,RMVar_hsa_circ_294472,RMVar_hsa_circ_50936,RMVar_hsa_circ_143703,RMVar_hsa_circ_143704,RMVar_hsa_circ_317897,RMVar_hsa_circ_321834,RMVar_hsa_circ_143709,RMVar_hsa_circ_143711,RMVar_hsa_circ_50317,RMVar_hsa_circ_341745,RMVar_hsa_circ_365812,RMVar_hsa_circ_271218,RMVar_hsa_circ_279810,RMVar_hsa_circ_311037,RMVar_hsa_circ_378339,RMVar_hsa_circ_143710,RMVar_hsa_circ_346845,RMVar_hsa_circ_272171,RMVar_hsa_circ_5411,RMVar_hsa_circ_143714,RMVar_hsa_circ_3277,RMVar_hsa_circ_143715,RMVar_hsa_circ_143716,RMVar_hsa_circ_291900,RMVar_hsa_circ_333341,RMVar_hsa_circ_374228,RMVar_hsa_circ_36837,RMVar_hsa_circ_143717,RMVar_hsa_circ_50659,RMVar_hsa_circ_312570,RMVar_hsa_circ_358261 22095 RMVar_ID_22095 Human_SNP_ID_436352499 A-to-I Human chr10 - 68042381 68042381 68042381 GACTCAAGGGATTCACCGGCTTTGGCCTCCCAAAGTGTTGAGATTACAGGCGTAAGCCACTGTGT GACTCAAGGGATTCACCGGCTTTGGCCTCCCACAGTGTTGAGATTACAGGCGTAAGCCACTGTGT T G HERC4 Ensembl:ENSG00000148634 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1564584297 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125199,RMVar_hsa_circ_143661,RMVar_hsa_circ_297679,RMVar_hsa_circ_97971,RMVar_hsa_circ_108552,RMVar_hsa_circ_143662,RMVar_hsa_circ_80660,RMVar_hsa_circ_143672,RMVar_hsa_circ_320283,RMVar_hsa_circ_277400,RMVar_hsa_circ_58500,RMVar_hsa_circ_143673,RMVar_hsa_circ_143674,RMVar_hsa_circ_72423,RMVar_hsa_circ_143682,RMVar_hsa_circ_372966,RMVar_hsa_circ_273519,RMVar_hsa_circ_143700,RMVar_hsa_circ_143685,RMVar_hsa_circ_143686,RMVar_hsa_circ_282075,RMVar_hsa_circ_143684,RMVar_hsa_circ_143695,RMVar_hsa_circ_344718,RMVar_hsa_circ_279414,RMVar_hsa_circ_143701,RMVar_hsa_circ_143702,RMVar_hsa_circ_27343,RMVar_hsa_circ_315590,RMVar_hsa_circ_72407,RMVar_hsa_circ_294561,RMVar_hsa_circ_294472,RMVar_hsa_circ_50936,RMVar_hsa_circ_143703,RMVar_hsa_circ_143704,RMVar_hsa_circ_317897,RMVar_hsa_circ_143711,RMVar_hsa_circ_50317,RMVar_hsa_circ_341745,RMVar_hsa_circ_365812,RMVar_hsa_circ_271218,RMVar_hsa_circ_378339,RMVar_hsa_circ_346845,RMVar_hsa_circ_272171,RMVar_hsa_circ_5411,RMVar_hsa_circ_143714,RMVar_hsa_circ_3277,RMVar_hsa_circ_143715,RMVar_hsa_circ_143716,RMVar_hsa_circ_291900,RMVar_hsa_circ_374228,RMVar_hsa_circ_36837,RMVar_hsa_circ_143717,RMVar_hsa_circ_312570,RMVar_hsa_circ_358261,RMVar_hsa_circ_24978,RMVar_hsa_circ_315242,RMVar_hsa_circ_346757,RMVar_hsa_circ_87653,RMVar_hsa_circ_143718,RMVar_hsa_circ_143719 22096 RMVar_ID_22096 Human_SNP_ID_436352513 A-to-I Human chr10 - 68042444 68042444 68042444 CAATTTTGTATTTTTTGTAGAGACAGAGTTTCACCATGTTGCCCAGCTGGTCTTAAATTCCTGGA CAATTTTGTATTTTTTGTAGAGACAGAGTTTCGCCATGTTGCCCAGCTGGTCTTAAATTCCTGGA T C HERC4 Ensembl:ENSG00000148634 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1176521759 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125199,RMVar_hsa_circ_143661,RMVar_hsa_circ_297679,RMVar_hsa_circ_97971,RMVar_hsa_circ_108552,RMVar_hsa_circ_143662,RMVar_hsa_circ_80660,RMVar_hsa_circ_143672,RMVar_hsa_circ_320283,RMVar_hsa_circ_277400,RMVar_hsa_circ_58500,RMVar_hsa_circ_143673,RMVar_hsa_circ_143674,RMVar_hsa_circ_72423,RMVar_hsa_circ_143682,RMVar_hsa_circ_372966,RMVar_hsa_circ_273519,RMVar_hsa_circ_143700,RMVar_hsa_circ_143685,RMVar_hsa_circ_143686,RMVar_hsa_circ_282075,RMVar_hsa_circ_143684,RMVar_hsa_circ_143695,RMVar_hsa_circ_344718,RMVar_hsa_circ_279414,RMVar_hsa_circ_143701,RMVar_hsa_circ_143702,RMVar_hsa_circ_27343,RMVar_hsa_circ_315590,RMVar_hsa_circ_72407,RMVar_hsa_circ_294561,RMVar_hsa_circ_294472,RMVar_hsa_circ_50936,RMVar_hsa_circ_143703,RMVar_hsa_circ_143704,RMVar_hsa_circ_317897,RMVar_hsa_circ_143711,RMVar_hsa_circ_50317,RMVar_hsa_circ_341745,RMVar_hsa_circ_365812,RMVar_hsa_circ_271218,RMVar_hsa_circ_378339,RMVar_hsa_circ_346845,RMVar_hsa_circ_272171,RMVar_hsa_circ_5411,RMVar_hsa_circ_143714,RMVar_hsa_circ_3277,RMVar_hsa_circ_143715,RMVar_hsa_circ_143716,RMVar_hsa_circ_291900,RMVar_hsa_circ_374228,RMVar_hsa_circ_36837,RMVar_hsa_circ_143717,RMVar_hsa_circ_312570,RMVar_hsa_circ_358261,RMVar_hsa_circ_24978,RMVar_hsa_circ_315242,RMVar_hsa_circ_346757,RMVar_hsa_circ_87653,RMVar_hsa_circ_143718,RMVar_hsa_circ_143719 22097 RMVar_ID_22097 Human_SNP_ID_436354184 A-to-I Human chr10 - 68049739 68049737 68049739 GCCTGGCTAATTTTTAATTTTTTTGTAGAGACAGGGTCTCATTATGTTGCCGAGGCTGGTTTCGA GCCTGGCTAATTTTTAATTTTTTTGTAGAGAC__GGTCTCATTATGTTGCCGAGGCTGGTTTCGA CCT C HERC4 Ensembl:ENSG00000148634 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs527806576 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_2226634,Human_RBP_ID_11495724 RMVar_hsa_circ_125199,RMVar_hsa_circ_143661,RMVar_hsa_circ_97971,RMVar_hsa_circ_108552,RMVar_hsa_circ_143662,RMVar_hsa_circ_320283,RMVar_hsa_circ_58500,RMVar_hsa_circ_72423,RMVar_hsa_circ_143682,RMVar_hsa_circ_372966,RMVar_hsa_circ_143684,RMVar_hsa_circ_344718,RMVar_hsa_circ_143702,RMVar_hsa_circ_27343,RMVar_hsa_circ_72407,RMVar_hsa_circ_294472,RMVar_hsa_circ_50936,RMVar_hsa_circ_50317,RMVar_hsa_circ_341745,RMVar_hsa_circ_365812,RMVar_hsa_circ_346845,RMVar_hsa_circ_5411,RMVar_hsa_circ_3277,RMVar_hsa_circ_143716,RMVar_hsa_circ_374228,RMVar_hsa_circ_36837,RMVar_hsa_circ_312570,RMVar_hsa_circ_6241,RMVar_hsa_circ_24978,RMVar_hsa_circ_346757,RMVar_hsa_circ_87653,RMVar_hsa_circ_143719 22098 RMVar_ID_22098 Human_SNP_ID_436354185 A-to-I Human chr10 - 68049739 68049739 68049739 GCCTGGCTAATTTTTAATTTTTTTGTAGAGACAGGGTCTCATTATGTTGCCGAGGCTGGTTTCGA GCCTGGCTAATTTTTAATTTTTTTGTAGAGACTGGGTCTCATTATGTTGCCGAGGCTGGTTTCGA T A HERC4 Ensembl:ENSG00000148634 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs753180198 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2226634,Human_RBP_ID_11495724 RMVar_hsa_circ_125199,RMVar_hsa_circ_143661,RMVar_hsa_circ_97971,RMVar_hsa_circ_108552,RMVar_hsa_circ_143662,RMVar_hsa_circ_320283,RMVar_hsa_circ_58500,RMVar_hsa_circ_72423,RMVar_hsa_circ_143682,RMVar_hsa_circ_372966,RMVar_hsa_circ_143684,RMVar_hsa_circ_344718,RMVar_hsa_circ_143702,RMVar_hsa_circ_27343,RMVar_hsa_circ_72407,RMVar_hsa_circ_294472,RMVar_hsa_circ_50936,RMVar_hsa_circ_50317,RMVar_hsa_circ_341745,RMVar_hsa_circ_365812,RMVar_hsa_circ_346845,RMVar_hsa_circ_5411,RMVar_hsa_circ_3277,RMVar_hsa_circ_143716,RMVar_hsa_circ_374228,RMVar_hsa_circ_36837,RMVar_hsa_circ_312570,RMVar_hsa_circ_6241,RMVar_hsa_circ_24978,RMVar_hsa_circ_346757,RMVar_hsa_circ_87653,RMVar_hsa_circ_143719 22099 RMVar_ID_22099 Human_SNP_ID_436354186 A-to-I Human chr10 - 68049739 68049739 68049739 GCCTGGCTAATTTTTAATTTTTTTGTAGAGACAGGGTCTCATTATGTTGCCGAGGCTGGTTTCGA GCCTGGCTAATTTTTAATTTTTTTGTAGAGACGGGGTCTCATTATGTTGCCGAGGCTGGTTTCGA T C HERC4 Ensembl:ENSG00000148634 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs753180198 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2226634,Human_RBP_ID_11495724 RMVar_hsa_circ_125199,RMVar_hsa_circ_143661,RMVar_hsa_circ_97971,RMVar_hsa_circ_108552,RMVar_hsa_circ_143662,RMVar_hsa_circ_320283,RMVar_hsa_circ_58500,RMVar_hsa_circ_72423,RMVar_hsa_circ_143682,RMVar_hsa_circ_372966,RMVar_hsa_circ_143684,RMVar_hsa_circ_344718,RMVar_hsa_circ_143702,RMVar_hsa_circ_27343,RMVar_hsa_circ_72407,RMVar_hsa_circ_294472,RMVar_hsa_circ_50936,RMVar_hsa_circ_50317,RMVar_hsa_circ_341745,RMVar_hsa_circ_365812,RMVar_hsa_circ_346845,RMVar_hsa_circ_5411,RMVar_hsa_circ_3277,RMVar_hsa_circ_143716,RMVar_hsa_circ_374228,RMVar_hsa_circ_36837,RMVar_hsa_circ_312570,RMVar_hsa_circ_6241,RMVar_hsa_circ_24978,RMVar_hsa_circ_346757,RMVar_hsa_circ_87653,RMVar_hsa_circ_143719 22100 RMVar_ID_22100 Human_SNP_ID_436354206 A-to-I Human chr10 - 68049835 68049835 68049835 ACAATCACGGCTCACTGTAGCCCTGACCTCATAGGCTTAAGAGATCCTCCCACCTCAATTCCCTG ACAATCACGGCTCACTGTAGCCCTGACCTCATGGGCTTAAGAGATCCTCCCACCTCAATTCCCTG T C HERC4 Ensembl:ENSG00000148634 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1046021673 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11394570 RMVar_hsa_circ_125199,RMVar_hsa_circ_143661,RMVar_hsa_circ_97971,RMVar_hsa_circ_108552,RMVar_hsa_circ_143662,RMVar_hsa_circ_320283,RMVar_hsa_circ_58500,RMVar_hsa_circ_72423,RMVar_hsa_circ_143682,RMVar_hsa_circ_372966,RMVar_hsa_circ_143684,RMVar_hsa_circ_344718,RMVar_hsa_circ_143702,RMVar_hsa_circ_27343,RMVar_hsa_circ_72407,RMVar_hsa_circ_294472,RMVar_hsa_circ_50936,RMVar_hsa_circ_50317,RMVar_hsa_circ_341745,RMVar_hsa_circ_365812,RMVar_hsa_circ_346845,RMVar_hsa_circ_5411,RMVar_hsa_circ_3277,RMVar_hsa_circ_143716,RMVar_hsa_circ_374228,RMVar_hsa_circ_36837,RMVar_hsa_circ_312570,RMVar_hsa_circ_6241,RMVar_hsa_circ_24978,RMVar_hsa_circ_346757,RMVar_hsa_circ_87653,RMVar_hsa_circ_143719 22101 RMVar_ID_22101 Human_SNP_ID_436357383 A-to-I Human chr10 - 68060326 68060326 68060326 GACTAAGGCAGGAGAATTGCTTGAACCCGGGAAGCAGAGGTTGCAGTGAATTGAGATCGTGCCAC GACTAAGGCAGGAGAATTGCTTGAACCCGGGAGGCAGAGGTTGCAGTGAATTGAGATCGTGCCAC T C HERC4 Ensembl:ENSG00000148634 Protein coding intron GSE38233;GSE107867 cultured B-cells;ASD brains,frontal_cortex - 24183664,30559470 RNA-Seq:(High) rs993041331 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125199,RMVar_hsa_circ_143661,RMVar_hsa_circ_97971,RMVar_hsa_circ_108552,RMVar_hsa_circ_143662,RMVar_hsa_circ_320283,RMVar_hsa_circ_58500,RMVar_hsa_circ_72423,RMVar_hsa_circ_143682,RMVar_hsa_circ_372966,RMVar_hsa_circ_143684,RMVar_hsa_circ_344718,RMVar_hsa_circ_143702,RMVar_hsa_circ_27343,RMVar_hsa_circ_72407,RMVar_hsa_circ_294472,RMVar_hsa_circ_50936,RMVar_hsa_circ_50317,RMVar_hsa_circ_341745,RMVar_hsa_circ_365812,RMVar_hsa_circ_346845,RMVar_hsa_circ_5411,RMVar_hsa_circ_3277,RMVar_hsa_circ_143716,RMVar_hsa_circ_374228,RMVar_hsa_circ_36837,RMVar_hsa_circ_312570,RMVar_hsa_circ_6241,RMVar_hsa_circ_24978,RMVar_hsa_circ_346757,RMVar_hsa_circ_87653,RMVar_hsa_circ_143719 22102 RMVar_ID_22102 Human_SNP_ID_436357393 A-to-I Human chr10 - 68060375 68060374 68060375 AAATTAGCTGGGTATGGTGGTGTGCATCTGTAATCCCAGCTACTTGGGAGACTAAGGCAGGAGAA AAATTAGCTGGGTATGGTGGTGTGCATCTGTA_TCCCAGCTACTTGGGAGACTAAGGCAGGAGAA AT A HERC4 Ensembl:ENSG00000148634 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1179770838 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_125199,RMVar_hsa_circ_143661,RMVar_hsa_circ_97971,RMVar_hsa_circ_108552,RMVar_hsa_circ_143662,RMVar_hsa_circ_320283,RMVar_hsa_circ_58500,RMVar_hsa_circ_72423,RMVar_hsa_circ_143682,RMVar_hsa_circ_372966,RMVar_hsa_circ_143684,RMVar_hsa_circ_344718,RMVar_hsa_circ_143702,RMVar_hsa_circ_27343,RMVar_hsa_circ_72407,RMVar_hsa_circ_294472,RMVar_hsa_circ_50936,RMVar_hsa_circ_50317,RMVar_hsa_circ_341745,RMVar_hsa_circ_365812,RMVar_hsa_circ_346845,RMVar_hsa_circ_5411,RMVar_hsa_circ_3277,RMVar_hsa_circ_143716,RMVar_hsa_circ_374228,RMVar_hsa_circ_36837,RMVar_hsa_circ_312570,RMVar_hsa_circ_6241,RMVar_hsa_circ_24978,RMVar_hsa_circ_346757,RMVar_hsa_circ_87653,RMVar_hsa_circ_143719 22103 RMVar_ID_22103 Human_SNP_ID_436357394 A-to-I Human chr10 - 68060375 68060375 68060375 AAATTAGCTGGGTATGGTGGTGTGCATCTGTAATCCCAGCTACTTGGGAGACTAAGGCAGGAGAA AAATTAGCTGGGTATGGTGGTGTGCATCTGTAGTCCCAGCTACTTGGGAGACTAAGGCAGGAGAA T C HERC4 Ensembl:ENSG00000148634 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1400510957 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125199,RMVar_hsa_circ_143661,RMVar_hsa_circ_97971,RMVar_hsa_circ_108552,RMVar_hsa_circ_143662,RMVar_hsa_circ_320283,RMVar_hsa_circ_58500,RMVar_hsa_circ_72423,RMVar_hsa_circ_143682,RMVar_hsa_circ_372966,RMVar_hsa_circ_143684,RMVar_hsa_circ_344718,RMVar_hsa_circ_143702,RMVar_hsa_circ_27343,RMVar_hsa_circ_72407,RMVar_hsa_circ_294472,RMVar_hsa_circ_50936,RMVar_hsa_circ_50317,RMVar_hsa_circ_341745,RMVar_hsa_circ_365812,RMVar_hsa_circ_346845,RMVar_hsa_circ_5411,RMVar_hsa_circ_3277,RMVar_hsa_circ_143716,RMVar_hsa_circ_374228,RMVar_hsa_circ_36837,RMVar_hsa_circ_312570,RMVar_hsa_circ_6241,RMVar_hsa_circ_24978,RMVar_hsa_circ_346757,RMVar_hsa_circ_87653,RMVar_hsa_circ_143719 22104 RMVar_ID_22104 Human_SNP_ID_436358347 A-to-I Human chr10 - 68063827 68063827 68063827 TCAAGTGATTCTCTTGCCTTGGCCTCCTGAGTAGCTGGGATTACAGATGCCCGTCAACATGCCCT TCAAGTGATTCTCTTGCCTTGGCCTCCTGAGTGGCTGGGATTACAGATGCCCGTCAACATGCCCT T C HERC4 Ensembl:ENSG00000148634 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1027281835 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125199,RMVar_hsa_circ_143661,RMVar_hsa_circ_97971,RMVar_hsa_circ_108552,RMVar_hsa_circ_143662,RMVar_hsa_circ_320283,RMVar_hsa_circ_58500,RMVar_hsa_circ_72423,RMVar_hsa_circ_143682,RMVar_hsa_circ_372966,RMVar_hsa_circ_143684,RMVar_hsa_circ_344718,RMVar_hsa_circ_143702,RMVar_hsa_circ_27343,RMVar_hsa_circ_72407,RMVar_hsa_circ_294472,RMVar_hsa_circ_50936,RMVar_hsa_circ_50317,RMVar_hsa_circ_341745,RMVar_hsa_circ_365812,RMVar_hsa_circ_346845,RMVar_hsa_circ_5411,RMVar_hsa_circ_3277,RMVar_hsa_circ_143716,RMVar_hsa_circ_374228,RMVar_hsa_circ_36837,RMVar_hsa_circ_312570,RMVar_hsa_circ_6241,RMVar_hsa_circ_24978,RMVar_hsa_circ_346757,RMVar_hsa_circ_87653,RMVar_hsa_circ_143719 22105 RMVar_ID_22105 Human_SNP_ID_436358348 A-to-I Human chr10 - 68063827 68063827 68063827 TCAAGTGATTCTCTTGCCTTGGCCTCCTGAGTAGCTGGGATTACAGATGCCCGTCAACATGCCCT TCAAGTGATTCTCTTGCCTTGGCCTCCTGAGTCGCTGGGATTACAGATGCCCGTCAACATGCCCT T G HERC4 Ensembl:ENSG00000148634 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1027281835 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125199,RMVar_hsa_circ_143661,RMVar_hsa_circ_97971,RMVar_hsa_circ_108552,RMVar_hsa_circ_143662,RMVar_hsa_circ_320283,RMVar_hsa_circ_58500,RMVar_hsa_circ_72423,RMVar_hsa_circ_143682,RMVar_hsa_circ_372966,RMVar_hsa_circ_143684,RMVar_hsa_circ_344718,RMVar_hsa_circ_143702,RMVar_hsa_circ_27343,RMVar_hsa_circ_72407,RMVar_hsa_circ_294472,RMVar_hsa_circ_50936,RMVar_hsa_circ_50317,RMVar_hsa_circ_341745,RMVar_hsa_circ_365812,RMVar_hsa_circ_346845,RMVar_hsa_circ_5411,RMVar_hsa_circ_3277,RMVar_hsa_circ_143716,RMVar_hsa_circ_374228,RMVar_hsa_circ_36837,RMVar_hsa_circ_312570,RMVar_hsa_circ_6241,RMVar_hsa_circ_24978,RMVar_hsa_circ_346757,RMVar_hsa_circ_87653,RMVar_hsa_circ_143719 22106 RMVar_ID_22106 Human_SNP_ID_436358612 A-to-I Human chr10 - 68064850 68064850 68064850 CTCCTGTCTCAGCCTCCTGAGTAGCTGGGATTACAGACGTGTGCCACCACTCCCAGCTAATTTTT CTCCTGTCTCAGCCTCCTGAGTAGCTGGGATTGCAGACGTGTGCCACCACTCCCAGCTAATTTTT T C HERC4 Ensembl:ENSG00000148634 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs939365750 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125199,RMVar_hsa_circ_143661,RMVar_hsa_circ_97971,RMVar_hsa_circ_108552,RMVar_hsa_circ_143662,RMVar_hsa_circ_320283,RMVar_hsa_circ_58500,RMVar_hsa_circ_72423,RMVar_hsa_circ_143682,RMVar_hsa_circ_372966,RMVar_hsa_circ_143684,RMVar_hsa_circ_344718,RMVar_hsa_circ_143702,RMVar_hsa_circ_27343,RMVar_hsa_circ_72407,RMVar_hsa_circ_294472,RMVar_hsa_circ_50936,RMVar_hsa_circ_50317,RMVar_hsa_circ_341745,RMVar_hsa_circ_365812,RMVar_hsa_circ_346845,RMVar_hsa_circ_5411,RMVar_hsa_circ_3277,RMVar_hsa_circ_143716,RMVar_hsa_circ_374228,RMVar_hsa_circ_36837,RMVar_hsa_circ_312570,RMVar_hsa_circ_6241,RMVar_hsa_circ_24978,RMVar_hsa_circ_346757,RMVar_hsa_circ_87653,RMVar_hsa_circ_143719 22107 RMVar_ID_22107 Human_SNP_ID_436358783 A-to-I Human chr10 - 68065629 68065629 68065629 TCTCGAAGTGATCCTCGCACCTCAGACTCCCAAAGTGCTGGGATTATAGGCATGAACCACCACGC TCTCGAAGTGATCCTCGCACCTCAGACTCCCAGAGTGCTGGGATTATAGGCATGAACCACCACGC T C HERC4 Ensembl:ENSG00000148634 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1348394737 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11394983 RMVar_hsa_circ_125199,RMVar_hsa_circ_143661,RMVar_hsa_circ_97971,RMVar_hsa_circ_108552,RMVar_hsa_circ_143662,RMVar_hsa_circ_320283,RMVar_hsa_circ_58500,RMVar_hsa_circ_72423,RMVar_hsa_circ_143682,RMVar_hsa_circ_372966,RMVar_hsa_circ_143684,RMVar_hsa_circ_344718,RMVar_hsa_circ_143702,RMVar_hsa_circ_27343,RMVar_hsa_circ_72407,RMVar_hsa_circ_294472,RMVar_hsa_circ_50936,RMVar_hsa_circ_50317,RMVar_hsa_circ_341745,RMVar_hsa_circ_365812,RMVar_hsa_circ_346845,RMVar_hsa_circ_5411,RMVar_hsa_circ_3277,RMVar_hsa_circ_143716,RMVar_hsa_circ_374228,RMVar_hsa_circ_36837,RMVar_hsa_circ_312570,RMVar_hsa_circ_6241,RMVar_hsa_circ_24978,RMVar_hsa_circ_346757,RMVar_hsa_circ_87653,RMVar_hsa_circ_143719 22108 RMVar_ID_22108 Human_SNP_ID_436365845 A-to-I Human chr10 + 68095313 68095313 68095313 TCGAGGCTGTAGTAAGAAGAGATCACTCTATTACACTCCAGCTTGGGTGACAGAGTCAGTCCCTG TCGAGGCTGTAGTAAGAAGAGATCACTCTATTCCACTCCAGCTTGGGTGACAGAGTCAGTCCCTG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs894657603 Functional Loss SNV dbSNP153 33..33 33 - - - 22109 RMVar_ID_22109 Human_SNP_ID_436366138 A-to-I Human chr10 + 68096441 68096441 68096441 AAAATTAGCCGGGCATGGTGGCAGCCGCCTGTAGTCCCAGCTACTCGGGAGACTGAGGCAGGAGA AAAATTAGCCGGGCATGGTGGCAGCCGCCTGTCGTCCCAGCTACTCGGGAGACTGAGGCAGGAGA A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1197025967 Functional Loss SNV dbSNP153 33..33 33 - - - 22110 RMVar_ID_22110 Human_SNP_ID_436367426 A-to-I Human chr10 + 68102215 68102215 68102215 CAGTGGCACAATCAAAGCTCATTGCAGCCTCCACCTCCCAGGCTCGATCCTCCTGCCTCAGCCTC CAGTGGCACAATCAAAGCTCATTGCAGCCTCCGCCTCCCAGGCTCGATCCTCCTGCCTCAGCCTC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs554532230 Functional Loss SNV dbSNP153 33..33 33 - - - 22111 RMVar_ID_22111 Human_SNP_ID_436370212 A-to-I Human chr10 + 68114442 68114442 68114442 ACAATCTCGGCTCACTGCAACTTTTGCCTCCTAGGTTCAAGCGATTCTCCTGTCTCAGCCTCCCA ACAATCTCGGCTCACTGCAACTTTTGCCTCCTGGGTTCAAGCGATTCTCCTGTCTCAGCCTCCCA A G MYPN Ensembl:ENSG00000138347 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1345430923 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107930,RMVar_hsa_circ_38368,RMVar_hsa_circ_39857,RMVar_hsa_circ_143722 22112 RMVar_ID_22112 Human_SNP_ID_436374342 A-to-I Human chr10 + 68131314 68131314 68131314 GGGAGGCTGAGGCAGGAGAATCGCTTGAACTCAGGATGTGGGGGTTGCAGTGAGCCGAGATCGTG GGGAGGCTGAGGCAGGAGAATCGCTTGAACTCCGGATGTGGGGGTTGCAGTGAGCCGAGATCGTG A C MYPN Ensembl:ENSG00000138347 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1419848053 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107930,RMVar_hsa_circ_143722,RMVar_hsa_circ_21761 22113 RMVar_ID_22113 Human_SNP_ID_436374343 A-to-I Human chr10 + 68131314 68131314 68131314 GGGAGGCTGAGGCAGGAGAATCGCTTGAACTCAGGATGTGGGGGTTGCAGTGAGCCGAGATCGTG GGGAGGCTGAGGCAGGAGAATCGCTTGAACTCGGGATGTGGGGGTTGCAGTGAGCCGAGATCGTG A G MYPN Ensembl:ENSG00000138347 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1419848053 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107930,RMVar_hsa_circ_143722,RMVar_hsa_circ_21761 22114 RMVar_ID_22114 Human_SNP_ID_436374779 A-to-I Human chr10 + 68133125 68133125 68133125 TCGACTCACTGTAACCACCACCTTCTTGGTTCAAGCAATTCTCCTGCCTCAGCCTCCGTAGTAGC TCGACTCACTGTAACCACCACCTTCTTGGTTCCAGCAATTCTCCTGCCTCAGCCTCCGTAGTAGC A C MYPN Ensembl:ENSG00000138347 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264858846 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11395714 RMVar_hsa_circ_107930,RMVar_hsa_circ_143722,RMVar_hsa_circ_21761 22115 RMVar_ID_22115 Human_SNP_ID_436374803 A-to-I Human chr10 + 68133225 68133225 68133225 TTTTTGTATGTTTAGTAGAGACGGGTTCTGCCATATTGGCCAAGCTAGTCTCGAACTCCTGACCT TTTTTGTATGTTTAGTAGAGACGGGTTCTGCCGTATTGGCCAAGCTAGTCTCGAACTCCTGACCT A G MYPN Ensembl:ENSG00000138347 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1272339909 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107930,RMVar_hsa_circ_143722,RMVar_hsa_circ_21761 22116 RMVar_ID_22116 Human_SNP_ID_436374819 A-to-I Human chr10 + 68133299 68133299 68133299 CACTTGCCTCAGCCTCCCAAAGTGCTGGGGTTACAGGTGTCAGCCACCATGCCCGGCCTATAGAC CACTTGCCTCAGCCTCCCAAAGTGCTGGGGTTGCAGGTGTCAGCCACCATGCCCGGCCTATAGAC A G MYPN Ensembl:ENSG00000138347 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1182663707 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107930,RMVar_hsa_circ_143722,RMVar_hsa_circ_21761 22117 RMVar_ID_22117 Human_SNP_ID_436375237 A-to-I Human chr10 + 68135135 68135135 68135135 TACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGATGGAGGTTTCACCATGTTAGCCAGGCTG TACCATGCCTGGCTAATTTTTGTATTTTTAGTGGAGATGGAGGTTTCACCATGTTAGCCAGGCTG A G MYPN Ensembl:ENSG00000138347 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1361932493 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11395728 RMVar_hsa_circ_107930,RMVar_hsa_circ_143722,RMVar_hsa_circ_21761 22118 RMVar_ID_22118 Human_SNP_ID_436394765 A-to-I Human chr10 - 68211506 68211506 68211506 CCTAGCAGAATATTCTCTACATAGAAAATGCAATTTGACCAATGATCTCAAAGCATTTCAAAGCT CCTAGCAGAATATTCTCTACATAGAAAATGCAGTTTGACCAATGATCTCAAAGCATTTCAAAGCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1032453827 Functional Loss SNV dbSNP153 33..33 33 - - - 22119 RMVar_ID_22119 Human_SNP_ID_436395549 A-to-I Human chr10 + 68214747 68214747 68214747 TTTTATAATTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAAGCTGGTCTCGAACTCCTAACCT TTTTATAATTTTAGTAGAGACGGGGTTTCACCCTGTTGGCCAAGCTGGTCTCGAACTCCTAACCT A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs957348882 Functional Loss SNV dbSNP153 33..33 33 - - - 22120 RMVar_ID_22120 Human_SNP_ID_436412098 A-to-I Human chr10 - 68284036 68284036 68284036 TCATGTTAAAAATCGAAAAATGGGCCAGGCGCAGTGGCTCATGCCTGTAATCGTAGCACTTTGAG TCATGTTAAAAATCGAAAAATGGGCCAGGCGCGGTGGCTCATGCCTGTAATCGTAGCACTTTGAG T C PBLD Ensembl:ENSG00000108187 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs577012195 Functional Loss SNV dbSNP153 33..33 33 - - - 22121 RMVar_ID_22121 Human_SNP_ID_436422160 A-to-I Human chr10 - 68326299 68326299 68326299 ACAGTGGCTCATGCCTGTAATCCCAGCACTCTAGTAGGCCGAAGCTGGCGGATCACTTGAGATCA ACAGTGGCTCATGCCTGTAATCCCAGCACTCTGGTAGGCCGAAGCTGGCGGATCACTTGAGATCA T C PBLD Ensembl:ENSG00000108187 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968776221 Functional Loss SNV dbSNP153 33..33 33 - - - 22122 RMVar_ID_22122 Human_SNP_ID_436429952 A-to-I Human chr10 - 68354975 68354975 68354975 GAGTGTGGTAGTGGGTGCCTGTAATCCCAGCCACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAG GAGTGTGGTAGTGGGTGCCTGTAATCCCAGCCGCTCAGGAGGCTGAGGCAGGAGAATTGCTTGAG T C RUFY2 Ensembl:ENSG00000204130 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1346836735 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14694,RMVar_hsa_circ_143742,RMVar_hsa_circ_143741,RMVar_hsa_circ_143743,RMVar_hsa_circ_21006,RMVar_hsa_circ_40026,RMVar_hsa_circ_362597,RMVar_hsa_circ_143744 22123 RMVar_ID_22123 Human_SNP_ID_436429964 A-to-I Human chr10 - 68355048 68355048 68355048 GAGGTCAGGAGTTTGAAACCAGCCTGGCCAACATGGTGAAATCCCATCTCTACTAAAAATACAAA GAGGTCAGGAGTTTGAAACCAGCCTGGCCAACGTGGTGAAATCCCATCTCTACTAAAAATACAAA T C RUFY2 Ensembl:ENSG00000204130 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs991278837 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14694,RMVar_hsa_circ_143742,RMVar_hsa_circ_143741,RMVar_hsa_circ_143743,RMVar_hsa_circ_21006,RMVar_hsa_circ_40026,RMVar_hsa_circ_362597,RMVar_hsa_circ_143744 22124 RMVar_ID_22124 Human_SNP_ID_436429965 A-to-I Human chr10 - 68355050 68355050 68355050 TTGAGGTCAGGAGTTTGAAACCAGCCTGGCCAACATGGTGAAATCCCATCTCTACTAAAAATACA TTGAGGTCAGGAGTTTGAAACCAGCCTGGCCAGCATGGTGAAATCCCATCTCTACTAAAAATACA T C RUFY2 Ensembl:ENSG00000204130 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs920885713 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14694,RMVar_hsa_circ_143742,RMVar_hsa_circ_143741,RMVar_hsa_circ_143743,RMVar_hsa_circ_21006,RMVar_hsa_circ_40026,RMVar_hsa_circ_362597,RMVar_hsa_circ_143744 22125 RMVar_ID_22125 Human_SNP_ID_436429969 A-to-I Human chr10 - 68355063 68355063 68355063 GCAGGTGGGTCATTTGAGGTCAGGAGTTTGAAACCAGCCTGGCCAACATGGTGAAATCCCATCTC GCAGGTGGGTCATTTGAGGTCAGGAGTTTGAATCCAGCCTGGCCAACATGGTGAAATCCCATCTC T A RUFY2 Ensembl:ENSG00000204130 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1026739506 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14694,RMVar_hsa_circ_143742,RMVar_hsa_circ_143741,RMVar_hsa_circ_143743,RMVar_hsa_circ_21006,RMVar_hsa_circ_40026,RMVar_hsa_circ_362597,RMVar_hsa_circ_143744 22126 RMVar_ID_22126 Human_SNP_ID_436431598 A-to-I Human chr10 - 68361227 68361227 68361227 TTGCCCAGGCTGGAGTGCAGTGGTGCTATCTCAGCTCACTGCAACCTCTGCCTCCTGGGTTCTTT TTGCCCAGGCTGGAGTGCAGTGGTGCTATCTCGGCTCACTGCAACCTCTGCCTCCTGGGTTCTTT T C RUFY2 Ensembl:ENSG00000204130 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1332003727 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_143742,RMVar_hsa_circ_19881,RMVar_hsa_circ_143743,RMVar_hsa_circ_21006,RMVar_hsa_circ_40026,RMVar_hsa_circ_362597,RMVar_hsa_circ_143744,RMVar_hsa_circ_275127,RMVar_hsa_circ_279711,RMVar_hsa_circ_313137,RMVar_hsa_circ_265547,RMVar_hsa_circ_143745,RMVar_hsa_circ_143746,RMVar_hsa_circ_143747 22127 RMVar_ID_22127 Human_SNP_ID_436438782 A-to-I Human chr10 - 68389000 68389000 68389000 TAGTCTCAGCTGCTCAGGAGGCTGAGGTGGGAAGATCACTTGAGCTCTGGAGGTTGAGGCTACAC TAGTCTCAGCTGCTCAGGAGGCTGAGGTGGGAGGATCACTTGAGCTCTGGAGGTTGAGGCTACAC T C RUFY2 Ensembl:ENSG00000204130 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1487444700 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1684,RMVar_hsa_circ_40026,RMVar_hsa_circ_362597,RMVar_hsa_circ_143744,RMVar_hsa_circ_313137,RMVar_hsa_circ_265547,RMVar_hsa_circ_302523,RMVar_hsa_circ_143747,RMVar_hsa_circ_295514,RMVar_hsa_circ_12288,RMVar_hsa_circ_143748,RMVar_hsa_circ_143749,RMVar_hsa_circ_338314,RMVar_hsa_circ_10333,RMVar_hsa_circ_364159,RMVar_hsa_circ_33836,RMVar_hsa_circ_22507,RMVar_hsa_circ_62171,RMVar_hsa_circ_143755,RMVar_hsa_circ_279272,RMVar_hsa_circ_321968,RMVar_hsa_circ_327675,RMVar_hsa_circ_343411,RMVar_hsa_circ_323133,RMVar_hsa_circ_62065,RMVar_hsa_circ_42091,RMVar_hsa_circ_143757,RMVar_hsa_circ_143759,RMVar_hsa_circ_143760,RMVar_hsa_circ_143758,RMVar_hsa_circ_323068,RMVar_hsa_circ_330504,RMVar_hsa_circ_143761,RMVar_hsa_circ_143762,RMVar_hsa_circ_69668 22128 RMVar_ID_22128 Human_SNP_ID_436441340 A-to-I Human chr10 - 68399272 68399272 68399272 GGAGGCTGAGATGGGTGGATTGCCTGAGCCCAAGAGTTCGAGACCAGCCTGGGCAACATGGCGAA GGAGGCTGAGATGGGTGGATTGCCTGAGCCCAGGAGTTCGAGACCAGCCTGGGCAACATGGCGAA T C RUFY2 Ensembl:ENSG00000204130 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350184586 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40026,RMVar_hsa_circ_362597,RMVar_hsa_circ_143744,RMVar_hsa_circ_313137,RMVar_hsa_circ_302523,RMVar_hsa_circ_143747,RMVar_hsa_circ_143748,RMVar_hsa_circ_33836,RMVar_hsa_circ_22507,RMVar_hsa_circ_279272,RMVar_hsa_circ_323133,RMVar_hsa_circ_42091,RMVar_hsa_circ_143759,RMVar_hsa_circ_143760,RMVar_hsa_circ_323068,RMVar_hsa_circ_143761,RMVar_hsa_circ_143767,RMVar_hsa_circ_305737,RMVar_hsa_circ_313450,RMVar_hsa_circ_143768,RMVar_hsa_circ_318012,RMVar_hsa_circ_345682,RMVar_hsa_circ_122975,RMVar_hsa_circ_143774,RMVar_hsa_circ_27973,RMVar_hsa_circ_143770,RMVar_hsa_circ_143771,RMVar_hsa_circ_319171,RMVar_hsa_circ_143772,RMVar_hsa_circ_143773,RMVar_hsa_circ_305953,RMVar_hsa_circ_317504,RMVar_hsa_circ_143775 22129 RMVar_ID_22129 Human_SNP_ID_436446101 A-to-I Human chr10 - 68416293 68416281 68416294 CCCAGCTAATTTTTGTATTTTTTTGTAAAGACAGGGTTTCACCATGTTGCCCAGGCTGGTTTTGA CCCAGCTAATTTTTGTATTTTTTTGTAAAGA_____________TGTTGCCCAGGCTGGTTTTGA ATGGTGAAACCCTG A DNA2 Ensembl:ENSG00000138346 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1448302884 Functional Loss DEL dbSNP153 32..44 33 - - - RMVar_hsa_circ_81122,RMVar_hsa_circ_116948,RMVar_hsa_circ_143779,RMVar_hsa_circ_143780 22130 RMVar_ID_22130 Human_SNP_ID_436446119 A-to-I Human chr10 - 68416371 68416371 68416371 CCCTCAATCTCCCAGGCTAAAGTGATCTTCCTACCTCAGCCTCCCCAGTAGCTGGGCCCACAGGT CCCTCAATCTCCCAGGCTAAAGTGATCTTCCTGCCTCAGCCTCCCCAGTAGCTGGGCCCACAGGT T C DNA2 Ensembl:ENSG00000138346 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1446139494 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81122,RMVar_hsa_circ_116948,RMVar_hsa_circ_143779,RMVar_hsa_circ_143780 22131 RMVar_ID_22131 Human_SNP_ID_436446651 A-to-I Human chr10 - 68418234 68418234 68418234 TAATTTTTGTACTTTTCTAGAGATGGGGTTTCACCATCTTGTCCAGGCTGGTCTCGAACTCCTGA TAATTTTTGTACTTTTCTAGAGATGGGGTTTCCCCATCTTGTCCAGGCTGGTCTCGAACTCCTGA T G DNA2 Ensembl:ENSG00000138346 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1305516878 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81122,RMVar_hsa_circ_116948,RMVar_hsa_circ_143779,RMVar_hsa_circ_265867,RMVar_hsa_circ_269327,RMVar_hsa_circ_143780,RMVar_hsa_circ_268367,RMVar_hsa_circ_265119 22132 RMVar_ID_22132 Human_SNP_ID_436447252 A-to-I Human chr10 - 68420450 68420450 68420450 TCACTGCAACCTCCGACTCCCAGATTCAAGCAATTCTCCTTCCTCAGCCTCCTGAGTAGCTAGGA TCACTGCAACCTCCGACTCCCAGATTCAAGCAGTTCTCCTTCCTCAGCCTCCTGAGTAGCTAGGA T C DNA2 Ensembl:ENSG00000138346 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1219408614 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20499,RMVar_hsa_circ_3370,RMVar_hsa_circ_81122,RMVar_hsa_circ_331452,RMVar_hsa_circ_269327,RMVar_hsa_circ_143780,RMVar_hsa_circ_265119,RMVar_hsa_circ_370626,RMVar_hsa_circ_278117,RMVar_hsa_circ_29376,RMVar_hsa_circ_143782,RMVar_hsa_circ_143783,RMVar_hsa_circ_143784,RMVar_hsa_circ_268190,RMVar_hsa_circ_371591,RMVar_hsa_circ_265603,RMVar_hsa_circ_143785 22133 RMVar_ID_22133 Human_SNP_ID_436447511 A-to-I Human chr10 - 68421519 68421519 68421519 GAACTCCTGGCTTCAAATGATCCGCCTGCTTCAGCCTCCCAGAGTGCTGGGATTATAGTGTGAGC GAACTCCTGGCTTCAAATGATCCGCCTGCTTCCGCCTCCCAGAGTGCTGGGATTATAGTGTGAGC T G DNA2 Ensembl:ENSG00000138346 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs891269554 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20499,RMVar_hsa_circ_3370,RMVar_hsa_circ_81122,RMVar_hsa_circ_331452,RMVar_hsa_circ_269327,RMVar_hsa_circ_143780,RMVar_hsa_circ_265119,RMVar_hsa_circ_370626,RMVar_hsa_circ_278117,RMVar_hsa_circ_29376,RMVar_hsa_circ_143782,RMVar_hsa_circ_143783,RMVar_hsa_circ_143784,RMVar_hsa_circ_268190,RMVar_hsa_circ_371591,RMVar_hsa_circ_265603,RMVar_hsa_circ_143786,RMVar_hsa_circ_143785,RMVar_hsa_circ_143787 22134 RMVar_ID_22134 Human_SNP_ID_436452581 A-to-I Human chr10 - 68440436 68440436 68440436 AATATTAGCTGGGCATGGTGGCAGGTGCCTGTAGTCCCAGCTACTCCCAAGGCTGAGGCAGGAGA AATATTAGCTGGGCATGGTGGCAGGTGCCTGTGGTCCCAGCTACTCCCAAGGCTGAGGCAGGAGA T C DNA2 Ensembl:ENSG00000138346 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs886805836 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3370,RMVar_hsa_circ_81122,RMVar_hsa_circ_331452,RMVar_hsa_circ_143780,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_31008,RMVar_hsa_circ_101313,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_300476,RMVar_hsa_circ_277662,RMVar_hsa_circ_143796,RMVar_hsa_circ_143798,RMVar_hsa_circ_143799,RMVar_hsa_circ_143797,RMVar_hsa_circ_60452,RMVar_hsa_circ_143795,RMVar_hsa_circ_318317,RMVar_hsa_circ_50387,RMVar_hsa_circ_28081,RMVar_hsa_circ_6231,RMVar_hsa_circ_143804,RMVar_hsa_circ_305904,RMVar_hsa_circ_319245,RMVar_hsa_circ_18386,RMVar_hsa_circ_143805,RMVar_hsa_circ_143806,RMVar_hsa_circ_351678,RMVar_hsa_circ_143808,RMVar_hsa_circ_143810,RMVar_hsa_circ_283516,RMVar_hsa_circ_294028,RMVar_hsa_circ_324781,RMVar_hsa_circ_346955,RMVar_hsa_circ_284704,RMVar_hsa_circ_143812,RMVar_hsa_circ_47562,RMVar_hsa_circ_143811,RMVar_hsa_circ_143809 22135 RMVar_ID_22135 Human_SNP_ID_436452740 A-to-I Human chr10 - 68441214 68441214 68441214 ACAGTGCTCCTGCCTCAACCTCCTGAGTAGCTAGGACCATAGGTGTGCACCACCAAACTTGGCTA ACAGTGCTCCTGCCTCAACCTCCTGAGTAGCTTGGACCATAGGTGTGCACCACCAAACTTGGCTA T A DNA2 Ensembl:ENSG00000138346 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1313478312 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11398468 RMVar_hsa_circ_3370,RMVar_hsa_circ_81122,RMVar_hsa_circ_331452,RMVar_hsa_circ_143780,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_31008,RMVar_hsa_circ_101313,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_300476,RMVar_hsa_circ_277662,RMVar_hsa_circ_143796,RMVar_hsa_circ_143798,RMVar_hsa_circ_143799,RMVar_hsa_circ_143797,RMVar_hsa_circ_60452,RMVar_hsa_circ_143795,RMVar_hsa_circ_318317,RMVar_hsa_circ_50387,RMVar_hsa_circ_28081,RMVar_hsa_circ_6231,RMVar_hsa_circ_143804,RMVar_hsa_circ_305904,RMVar_hsa_circ_319245,RMVar_hsa_circ_18386,RMVar_hsa_circ_143805,RMVar_hsa_circ_143806,RMVar_hsa_circ_351678,RMVar_hsa_circ_143808,RMVar_hsa_circ_143810,RMVar_hsa_circ_283516,RMVar_hsa_circ_294028,RMVar_hsa_circ_324781,RMVar_hsa_circ_346955,RMVar_hsa_circ_284704,RMVar_hsa_circ_143812,RMVar_hsa_circ_47562,RMVar_hsa_circ_143811,RMVar_hsa_circ_143809 22136 RMVar_ID_22136 Human_SNP_ID_436454832 A-to-I Human chr10 - 68448899 68448899 68448899 TGGTGTGGTGGCACATGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGAATTGCTCAAACCAGGGA TGGTGTGGTGGCACATGCCTGTAGTCCCAGCTGCTCGGGAGGCTGAGAATTGCTCAAACCAGGGA T C DNA2 Ensembl:ENSG00000138346 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1564890295 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3370,RMVar_hsa_circ_81122,RMVar_hsa_circ_331452,RMVar_hsa_circ_143780,RMVar_hsa_circ_143784,RMVar_hsa_circ_371591,RMVar_hsa_circ_24880,RMVar_hsa_circ_143785,RMVar_hsa_circ_347913,RMVar_hsa_circ_31008,RMVar_hsa_circ_101313,RMVar_hsa_circ_143791,RMVar_hsa_circ_369697,RMVar_hsa_circ_8944,RMVar_hsa_circ_45606,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_315369,RMVar_hsa_circ_321724,RMVar_hsa_circ_277662,RMVar_hsa_circ_143796,RMVar_hsa_circ_143797,RMVar_hsa_circ_60452,RMVar_hsa_circ_143795,RMVar_hsa_circ_318317,RMVar_hsa_circ_28081,RMVar_hsa_circ_6231,RMVar_hsa_circ_143804,RMVar_hsa_circ_319245,RMVar_hsa_circ_143806,RMVar_hsa_circ_351678,RMVar_hsa_circ_143808,RMVar_hsa_circ_143810,RMVar_hsa_circ_283516,RMVar_hsa_circ_324781,RMVar_hsa_circ_346955,RMVar_hsa_circ_47562,RMVar_hsa_circ_327005,RMVar_hsa_circ_338150,RMVar_hsa_circ_143809,RMVar_hsa_circ_357456,RMVar_hsa_circ_283193,RMVar_hsa_circ_269945,RMVar_hsa_circ_143816,RMVar_hsa_circ_143813,RMVar_hsa_circ_143814,RMVar_hsa_circ_143815,RMVar_hsa_circ_314867,RMVar_hsa_circ_338359,RMVar_hsa_circ_52349,RMVar_hsa_circ_143817,RMVar_hsa_circ_319127 22137 RMVar_ID_22137 Human_SNP_ID_436454836 A-to-I Human chr10 - 68448909 68448909 68448909 CACACACACCTGGTGTGGTGGCACATGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGAATTGCTC CACACACACCTGGTGTGGTGGCACATGCCTGTTGTCCCAGCTACTCGGGAGGCTGAGAATTGCTC T A DNA2 Ensembl:ENSG00000138346 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1462027979 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3370,RMVar_hsa_circ_81122,RMVar_hsa_circ_331452,RMVar_hsa_circ_143780,RMVar_hsa_circ_143784,RMVar_hsa_circ_371591,RMVar_hsa_circ_24880,RMVar_hsa_circ_143785,RMVar_hsa_circ_347913,RMVar_hsa_circ_31008,RMVar_hsa_circ_101313,RMVar_hsa_circ_143791,RMVar_hsa_circ_369697,RMVar_hsa_circ_8944,RMVar_hsa_circ_45606,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_315369,RMVar_hsa_circ_321724,RMVar_hsa_circ_277662,RMVar_hsa_circ_143796,RMVar_hsa_circ_143797,RMVar_hsa_circ_60452,RMVar_hsa_circ_143795,RMVar_hsa_circ_318317,RMVar_hsa_circ_28081,RMVar_hsa_circ_6231,RMVar_hsa_circ_143804,RMVar_hsa_circ_319245,RMVar_hsa_circ_143806,RMVar_hsa_circ_351678,RMVar_hsa_circ_143808,RMVar_hsa_circ_143810,RMVar_hsa_circ_283516,RMVar_hsa_circ_324781,RMVar_hsa_circ_346955,RMVar_hsa_circ_47562,RMVar_hsa_circ_327005,RMVar_hsa_circ_338150,RMVar_hsa_circ_143809,RMVar_hsa_circ_357456,RMVar_hsa_circ_283193,RMVar_hsa_circ_269945,RMVar_hsa_circ_143816,RMVar_hsa_circ_143813,RMVar_hsa_circ_143814,RMVar_hsa_circ_143815,RMVar_hsa_circ_314867,RMVar_hsa_circ_338359,RMVar_hsa_circ_52349,RMVar_hsa_circ_143817,RMVar_hsa_circ_319127 22138 RMVar_ID_22138 Human_SNP_ID_436456759 A-to-I Human chr10 - 68456165 68456165 68456165 CAGACTGGAGTGCAGTGGTGTGATTTAGGCTCACTGCAACCTCTGCCTCCTGAGTTCAAACAGTC CAGACTGGAGTGCAGTGGTGTGATTTAGGCTCTCTGCAACCTCTGCCTCCTGAGTTCAAACAGTC T A DNA2 Ensembl:ENSG00000138346 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277999809 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81122,RMVar_hsa_circ_331452,RMVar_hsa_circ_143780,RMVar_hsa_circ_143784,RMVar_hsa_circ_371591,RMVar_hsa_circ_143785,RMVar_hsa_circ_347913,RMVar_hsa_circ_31008,RMVar_hsa_circ_143791,RMVar_hsa_circ_369697,RMVar_hsa_circ_8944,RMVar_hsa_circ_45606,RMVar_hsa_circ_122574,RMVar_hsa_circ_121562,RMVar_hsa_circ_143793,RMVar_hsa_circ_143794,RMVar_hsa_circ_315369,RMVar_hsa_circ_321724,RMVar_hsa_circ_277662,RMVar_hsa_circ_143796,RMVar_hsa_circ_143797,RMVar_hsa_circ_60452,RMVar_hsa_circ_143795,RMVar_hsa_circ_318317,RMVar_hsa_circ_28081,RMVar_hsa_circ_6231,RMVar_hsa_circ_143804,RMVar_hsa_circ_319245,RMVar_hsa_circ_143806,RMVar_hsa_circ_351678,RMVar_hsa_circ_143808,RMVar_hsa_circ_143810,RMVar_hsa_circ_283516,RMVar_hsa_circ_324781,RMVar_hsa_circ_47562,RMVar_hsa_circ_338150,RMVar_hsa_circ_143809,RMVar_hsa_circ_357456,RMVar_hsa_circ_283193,RMVar_hsa_circ_269945,RMVar_hsa_circ_143816,RMVar_hsa_circ_143814,RMVar_hsa_circ_143815,RMVar_hsa_circ_314867,RMVar_hsa_circ_338359,RMVar_hsa_circ_52349,RMVar_hsa_circ_272182,RMVar_hsa_circ_143817,RMVar_hsa_circ_319127,RMVar_hsa_circ_332567,RMVar_hsa_circ_334702,RMVar_hsa_circ_300432,RMVar_hsa_circ_143819,RMVar_hsa_circ_143820,RMVar_hsa_circ_143818 22139 RMVar_ID_22139 Human_SNP_ID_436459164 A-to-I Human chr10 - 68464428 68464428 68464428 TCATTGCAGCCTCTACCTCCCGGGTTCAAGCAATTTTCCTGCCTCAGCCTCTCGAGTAGCTGGGA TCATTGCAGCCTCTACCTCCCGGGTTCAAGCAGTTTTCCTGCCTCAGCCTCTCGAGTAGCTGGGA T C DNA2 Ensembl:ENSG00000138346 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1329510313 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81122,RMVar_hsa_circ_331452,RMVar_hsa_circ_143780,RMVar_hsa_circ_143784,RMVar_hsa_circ_371591,RMVar_hsa_circ_143785,RMVar_hsa_circ_347913,RMVar_hsa_circ_143791,RMVar_hsa_circ_369697,RMVar_hsa_circ_8944,RMVar_hsa_circ_45606,RMVar_hsa_circ_122574,RMVar_hsa_circ_121562,RMVar_hsa_circ_143793,RMVar_hsa_circ_143794,RMVar_hsa_circ_321724,RMVar_hsa_circ_277662,RMVar_hsa_circ_143796,RMVar_hsa_circ_60452,RMVar_hsa_circ_143795,RMVar_hsa_circ_318317,RMVar_hsa_circ_6231,RMVar_hsa_circ_143804,RMVar_hsa_circ_319245,RMVar_hsa_circ_143806,RMVar_hsa_circ_351678,RMVar_hsa_circ_143808,RMVar_hsa_circ_283516,RMVar_hsa_circ_47562,RMVar_hsa_circ_143809,RMVar_hsa_circ_357456,RMVar_hsa_circ_283193,RMVar_hsa_circ_269945,RMVar_hsa_circ_143821,RMVar_hsa_circ_143816,RMVar_hsa_circ_143814,RMVar_hsa_circ_143815,RMVar_hsa_circ_314867,RMVar_hsa_circ_338359,RMVar_hsa_circ_272182,RMVar_hsa_circ_143817,RMVar_hsa_circ_319127,RMVar_hsa_circ_334702,RMVar_hsa_circ_300432,RMVar_hsa_circ_143819,RMVar_hsa_circ_143820,RMVar_hsa_circ_143823,RMVar_hsa_circ_293415,RMVar_hsa_circ_306271,RMVar_hsa_circ_340697,RMVar_hsa_circ_300252,RMVar_hsa_circ_143824,RMVar_hsa_circ_143822 22140 RMVar_ID_22140 Human_SNP_ID_436463204 A-to-I Human chr10 - 68478863 68478862 68478863 GTCCCAGCTACTTGGGAGGCTGAGGTAGGAGAATTGCTTGAACCCAGAAGGCGGAGGTTGCAGTG GTCCCAGCTACTTGGGAGGCTGAGGTAGGAGA_TTGCTTGAACCCAGAAGGCGGAGGTTGCAGTG AT A SLC25A16 Ensembl:ENSG00000122912 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1454561718 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_143828,RMVar_hsa_circ_143829 22141 RMVar_ID_22141 Human_SNP_ID_436463219 A-to-I Human chr10 - 68478918 68478918 68478918 TCCCATCTCTACTAAAAATATAAAAATTAGCCAGGCATGGTGGTGGGCGCCTGTAGTCCCAGCTA TCCCATCTCTACTAAAAATATAAAAATTAGCCGGGCATGGTGGTGGGCGCCTGTAGTCCCAGCTA T C SLC25A16 Ensembl:ENSG00000122912 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1332914772 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_143828,RMVar_hsa_circ_143829 22142 RMVar_ID_22142 Human_SNP_ID_436463224 A-to-I Human chr10 - 68478937 68478937 68478937 CCTGGCCAACATGGTGAAATCCCATCTCTACTAAAAATATAAAAATTAGCCAGGCATGGTGGTGG CCTGGCCAACATGGTGAAATCCCATCTCTACTGAAAATATAAAAATTAGCCAGGCATGGTGGTGG T C SLC25A16 Ensembl:ENSG00000122912 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs558636016 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_143828,RMVar_hsa_circ_143829 22143 RMVar_ID_22143 Human_SNP_ID_436463376 A-to-I Human chr10 - 68479560 68479560 68479560 CCTCAAGTGATCTGCCCCCCCGACTTCCCAAAATGCTGGGACTACTGGCATGAGCCAGTGCTCCT CCTCAAGTGATCTGCCCCCCCGACTTCCCAAAGTGCTGGGACTACTGGCATGAGCCAGTGCTCCT T C SLC25A16 Ensembl:ENSG00000122912 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1179188291 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_143828,RMVar_hsa_circ_143829 22144 RMVar_ID_22144 Human_SNP_ID_436463377 A-to-I Human chr10 - 68479563 68479563 68479563 TGACCTCAAGTGATCTGCCCCCCCGACTTCCCAAAATGCTGGGACTACTGGCATGAGCCAGTGCT TGACCTCAAGTGATCTGCCCCCCCGACTTCCCGAAATGCTGGGACTACTGGCATGAGCCAGTGCT T C SLC25A16 Ensembl:ENSG00000122912 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992298191 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23152396 RMVar_hsa_circ_143828,RMVar_hsa_circ_143829 22145 RMVar_ID_22145 Human_SNP_ID_436463406 A-to-I Human chr10 - 68479588 68479588 68479588 GTTGGCCAGGCTGGTCTTGAATACCTGACCTCAAGTGATCTGCCCCCCCGACTTCCCAAAATGCT GTTGGCCAGGCTGGTCTTGAATACCTGACCTCCAGTGATCTGCCCCCCCGACTTCCCAAAATGCT T G SLC25A16 Ensembl:ENSG00000122912 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1247321070 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_143828,RMVar_hsa_circ_143829 22146 RMVar_ID_22146 Human_SNP_ID_436463418 A-to-I Human chr10 - 68479645 68479645 68479645 CACCCGCCACCACGCCCAGCTAATTTTTGTGTATTTAGTAGAGCTGGGTTTTGCCCTGTTGGCCA CACCCGCCACCACGCCCAGCTAATTTTTGTGTCTTTAGTAGAGCTGGGTTTTGCCCTGTTGGCCA T G SLC25A16 Ensembl:ENSG00000122912 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1385688285 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5990220 RMVar_hsa_circ_143828,RMVar_hsa_circ_143829 22147 RMVar_ID_22147 Human_SNP_ID_436463451 A-to-I Human chr10 - 68479747 68479747 68479747 CAGGCTGGAGTGCAGTGGTGTGATCTCAGCTCACTGCAACCTCCACCTCCTGGGTTCTAGCGATT CAGGCTGGAGTGCAGTGGTGTGATCTCAGCTCGCTGCAACCTCCACCTCCTGGGTTCTAGCGATT T C SLC25A16 Ensembl:ENSG00000122912 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1326347487 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_143828,RMVar_hsa_circ_143829 22148 RMVar_ID_22148 Human_SNP_ID_436463463 A-to-I Human chr10 - 68479804 68479804 68479804 CTTTTTTTTTTTTTTTTTTGAGACAGAGCCTCACTCTGTTGCCCAGGCTGGAGTGCCCAGGCTGG CTTTTTTTTTTTTTTTTTTGAGACAGAGCCTCTCTCTGTTGCCCAGGCTGGAGTGCCCAGGCTGG T A SLC25A16 Ensembl:ENSG00000122912 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1385462668 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_143828,RMVar_hsa_circ_143829 22149 RMVar_ID_22149 Human_SNP_ID_436463464 A-to-I Human chr10 - 68479804 68479804 68479804 CTTTTTTTTTTTTTTTTTTGAGACAGAGCCTCACTCTGTTGCCCAGGCTGGAGTGCCCAGGCTGG CTTTTTTTTTTTTTTTTTTGAGACAGAGCCTCGCTCTGTTGCCCAGGCTGGAGTGCCCAGGCTGG T C SLC25A16 Ensembl:ENSG00000122912 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1385462668 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_143828,RMVar_hsa_circ_143829 22150 RMVar_ID_22150 Human_SNP_ID_436463465 A-to-I Human chr10 - 68479804 68479804 68479804 CTTTTTTTTTTTTTTTTTTGAGACAGAGCCTCACTCTGTTGCCCAGGCTGGAGTGCCCAGGCTGG CTTTTTTTTTTTTTTTTTTGAGACAGAGCCTCCCTCTGTTGCCCAGGCTGGAGTGCCCAGGCTGG T G SLC25A16 Ensembl:ENSG00000122912 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1385462668 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_143828,RMVar_hsa_circ_143829 22151 RMVar_ID_22151 Human_SNP_ID_436463469 A-to-I Human chr10 - 68479816 68479815 68479816 TTTCTTTTCTTTCTTTTTTTTTTTTTTTTTTGAGACAGAGCCTCACTCTGTTGCCCAGGCTGGAG TTTCTTTTCTTTCTTTTTTTTTTTTTTTTTTG_GACAGAGCCTCACTCTGTTGCCCAGGCTGGAG CT C SLC25A16 Ensembl:ENSG00000122912 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1221837879 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_11399266 RMVar_hsa_circ_143828,RMVar_hsa_circ_143829 22152 RMVar_ID_22152 Human_SNP_ID_436463521 A-to-I Human chr10 - 68479942 68479942 68479942 CAGTGGTGCAATCTCGGCTCACTGCAATCTCCACCTCCGGGTTCAAGCGATTTTCCCGAGTCATC CAGTGGTGCAATCTCGGCTCACTGCAATCTCCCCCTCCGGGTTCAAGCGATTTTCCCGAGTCATC T G SLC25A16 Ensembl:ENSG00000122912 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1450903639 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_143828,RMVar_hsa_circ_143829 22153 RMVar_ID_22153 Human_SNP_ID_436463523 A-to-I Human chr10 - 68479948 68479948 68479948 GGAGTGCAGTGGTGCAATCTCGGCTCACTGCAATCTCCACCTCCGGGTTCAAGCGATTTTCCCGA GGAGTGCAGTGGTGCAATCTCGGCTCACTGCAGTCTCCACCTCCGGGTTCAAGCGATTTTCCCGA T C SLC25A16 Ensembl:ENSG00000122912 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1224478632 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_143828,RMVar_hsa_circ_143829 22154 RMVar_ID_22154 Human_SNP_ID_436463540 A-to-I Human chr10 - 68479998 68479998 68479998 ATTCTTTTTTTTTTTTTTTTAACGAGAGTCTTAACTCTGTCACCCAAGCTGGAGTGCAGTGGTGC ATTCTTTTTTTTTTTTTTTTAACGAGAGTCTTCACTCTGTCACCCAAGCTGGAGTGCAGTGGTGC T G SLC25A16 Ensembl:ENSG00000122912 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1433208413 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11399267 RMVar_hsa_circ_143828,RMVar_hsa_circ_143829 22155 RMVar_ID_22155 Human_SNP_ID_436463740 A-to-I Human chr10 - 68480621 68480621 68480621 GTGGTGGCACGCACCTGTAGTCCCAGTTACTCAGGAGGCTGAGACAGGAGAATCACTTGAACCTG GTGGTGGCACGCACCTGTAGTCCCAGTTACTCGGGAGGCTGAGACAGGAGAATCACTTGAACCTG T C SLC25A16 Ensembl:ENSG00000122912 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10998213 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_143828,RMVar_hsa_circ_143829 22156 RMVar_ID_22156 Human_SNP_ID_436463741 A-to-I Human chr10 - 68480621 68480621 68480621 GTGGTGGCACGCACCTGTAGTCCCAGTTACTCAGGAGGCTGAGACAGGAGAATCACTTGAACCTG GTGGTGGCACGCACCTGTAGTCCCAGTTACTCCGGAGGCTGAGACAGGAGAATCACTTGAACCTG T G SLC25A16 Ensembl:ENSG00000122912 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10998213 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_143828,RMVar_hsa_circ_143829 22157 RMVar_ID_22157 Human_SNP_ID_436463757 A-to-I Human chr10 - 68480674 68480674 68480674 GGCTAACACGGTGAAAACCTATCTCTACTAAAAATACAAAAAATTAGCTGGGCGTGGTGGCACGC GGCTAACACGGTGAAAACCTATCTCTACTAAAGATACAAAAAATTAGCTGGGCGTGGTGGCACGC T C SLC25A16 Ensembl:ENSG00000122912 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs914854740 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_143828,RMVar_hsa_circ_143829 22158 RMVar_ID_22158 Human_SNP_ID_436463758 A-to-I Human chr10 - 68480674 68480674 68480674 GGCTAACACGGTGAAAACCTATCTCTACTAAAAATACAAAAAATTAGCTGGGCGTGGTGGCACGC GGCTAACACGGTGAAAACCTATCTCTACTAAACATACAAAAAATTAGCTGGGCGTGGTGGCACGC T G SLC25A16 Ensembl:ENSG00000122912 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs914854740 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_143828,RMVar_hsa_circ_143829 22159 RMVar_ID_22159 Human_SNP_ID_436463867 A-to-I Human chr10 - 68480987 68480987 68480987 TGTATAAAAGCCTGTATAAAAATTTCTTTTATACAGAGTGAGACTGTATAAAAGAAAAAAAAAGG TGTATAAAAGCCTGTATAAAAATTTCTTTTATGCAGAGTGAGACTGTATAAAAGAAAAAAAAAGG T C SLC25A16 Ensembl:ENSG00000122912 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1490809291 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_143828,RMVar_hsa_circ_143829 22160 RMVar_ID_22160 Human_SNP_ID_436463896 A-to-I Human chr10 - 68481122 68481122 68481122 AAATCAGCCGGGCATGGTGGCGGGCGCCTGTAATCCCAGCTACTTGGGAGGCTAAGGCAGGGAGA AAATCAGCCGGGCATGGTGGCGGGCGCCTGTATTCCCAGCTACTTGGGAGGCTAAGGCAGGGAGA T A SLC25A16 Ensembl:ENSG00000122912 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs549346616 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24825029 RMVar_hsa_circ_143828,RMVar_hsa_circ_143829 22161 RMVar_ID_22161 Human_SNP_ID_436463999 A-to-I Human chr10 - 68481572 68481572 68481572 GTTGAGTCCAGGCGTGGTGGCTCTTGCCTGTAACCCTAGCACTTTGGGAGGCTGAGGCGGGAGGA GTTGAGTCCAGGCGTGGTGGCTCTTGCCTGTAGCCCTAGCACTTTGGGAGGCTGAGGCGGGAGGA T C SLC25A16 Ensembl:ENSG00000122912 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs569192662 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_380327 RMVar_hsa_circ_143828,RMVar_hsa_circ_143829 22162 RMVar_ID_22162 Human_SNP_ID_436464034 A-to-I Human chr10 - 68481729 68481729 68481729 CGTGCCTGTAGTCCCAGTTACTCGCGAGGCTGAGACATGAGAATTGCTTGAGCTCGGGAAGCGGA CGTGCCTGTAGTCCCAGTTACTCGCGAGGCTGGGACATGAGAATTGCTTGAGCTCGGGAAGCGGA T C SLC25A16 Ensembl:ENSG00000122912 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1349817739 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5990235 RMVar_hsa_circ_143828,RMVar_hsa_circ_143829 22163 RMVar_ID_22163 Human_SNP_ID_436464060 A-to-I Human chr10 - 68481792 68481792 68481792 TAAGATCAGCATGGTGAAACCCCACCTCTACTAAAAATACAAAAAGTAGCAGGTGTGGTGGCTCG TAAGATCAGCATGGTGAAACCCCACCTCTACTGAAAATACAAAAAGTAGCAGGTGTGGTGGCTCG T C SLC25A16 Ensembl:ENSG00000122912 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1367287612 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_143828,RMVar_hsa_circ_143829 22164 RMVar_ID_22164 Human_SNP_ID_436464073 A-to-I Human chr10 - 68481877 68481877 68481877 TTAGAAGGCCAGGTGTGGTGGCTCACGCCTTTATTCCCAGCACTTTGGGAGGCCGAGTTGGGTGG TTAGAAGGCCAGGTGTGGTGGCTCACGCCTTTTTTCCCAGCACTTTGGGAGGCCGAGTTGGGTGG T A SLC25A16 Ensembl:ENSG00000122912 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934683369 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24825037 RMVar_hsa_circ_143828,RMVar_hsa_circ_143829 22165 RMVar_ID_22165 Human_SNP_ID_436464110 A-to-I Human chr10 - 68481984 68481984 68481984 GGCCTCGATCTCCTGAACCTCATGATCTGCCCACCTTGGTCTCCCAAAGTGCTGAGATTACTGGC GGCCTCGATCTCCTGAACCTCATGATCTGCCCTCCTTGGTCTCCCAAAGTGCTGAGATTACTGGC T A SLC25A16 Ensembl:ENSG00000122912 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1007141784 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_143828,RMVar_hsa_circ_143829 22166 RMVar_ID_22166 Human_SNP_ID_436464127 A-to-I Human chr10 - 68482047 68482047 68482047 AAATTCGCCTGGCTAATTTTTGTATTTTTAGTAGAGACGGGATTTCACCGTGTTAGCCAGGATGG AAATTCGCCTGGCTAATTTTTGTATTTTTAGTGGAGACGGGATTTCACCGTGTTAGCCAGGATGG T C SLC25A16 Ensembl:ENSG00000122912 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs779643287 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_143828,RMVar_hsa_circ_143829 22167 RMVar_ID_22167 Human_SNP_ID_436464131 A-to-I Human chr10 - 68482065 68482065 68482065 ACAGGTGCCCACCACCAAAAATTCGCCTGGCTAATTTTTGTATTTTTAGTAGAGACGGGATTTCA ACAGGTGCCCACCACCAAAAATTCGCCTGGCTGATTTTTGTATTTTTAGTAGAGACGGGATTTCA T C SLC25A16 Ensembl:ENSG00000122912 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1224155805 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_143828,RMVar_hsa_circ_143829 22168 RMVar_ID_22168 Human_SNP_ID_436464474 A-to-I Human chr10 - 68483508 68483508 68483508 AAAAGGACTCTATCGTGGTTTATCTCTTAATTACATTCGCTGTATTCCCTCTCAAGCAGTGGCTT AAAAGGACTCTATCGTGGTTTATCTCTTAATTGCATTCGCTGTATTCCCTCTCAAGCAGTGGCTT T C SLC25A16 Ensembl:ENSG00000122912 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs373242003 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_380344,Human_RBP_ID_1769261,Human_RBP_ID_3354941,Human_RBP_ID_5990253,Human_RBP_ID_8057498,Human_RBP_ID_8762355,Human_RBP_ID_8991288,Human_RBP_ID_17344412,Human_RBP_ID_17460484,Human_RBP_ID_18596545,Human_RBP_ID_23265394,Human_RBP_ID_27194144 Human_Splice_Rec_1139574,Human_Splice_Rec_1139588,Human_Splice_Rec_1139606 Human_miRNA_ID_2562230 RMVar_hsa_circ_143830,RMVar_hsa_circ_143828,RMVar_hsa_circ_143829,RMVar_hsa_circ_143832,RMVar_hsa_circ_143834,RMVar_hsa_circ_269316,RMVar_hsa_circ_269457,RMVar_hsa_circ_378669,RMVar_hsa_circ_143833,RMVar_hsa_circ_143831 22169 RMVar_ID_22169 Human_SNP_ID_436464921 A-to-I Human chr10 - 68485254 68485254 68485254 AACCCCATCTCTACTAAAAATACAAAAAAATTAGCTGGGTGTGGCGGTGTGCGCCTGTAGTCCCA AACCCCATCTCTACTAAAAATACAAAAAAATTGGCTGGGTGTGGCGGTGTGCGCCTGTAGTCCCA T C SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1186752741 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_143830,RMVar_hsa_circ_143828,RMVar_hsa_circ_143829,RMVar_hsa_circ_143832,RMVar_hsa_circ_143834,RMVar_hsa_circ_269316,RMVar_hsa_circ_269457,RMVar_hsa_circ_378669,RMVar_hsa_circ_143833,RMVar_hsa_circ_143831 22170 RMVar_ID_22170 Human_SNP_ID_436464929 A-to-I Human chr10 - 68485293 68485293 68485293 AAGGTCAGGAGATCAAGACCATCCTGGTCAACATGGTGAAACCCCATCTCTACTAAAAATACAAA AAGGTCAGGAGATCAAGACCATCCTGGTCAACGTGGTGAAACCCCATCTCTACTAAAAATACAAA T C SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1263432226 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_143830,RMVar_hsa_circ_143828,RMVar_hsa_circ_143829,RMVar_hsa_circ_143832,RMVar_hsa_circ_143834,RMVar_hsa_circ_269316,RMVar_hsa_circ_269457,RMVar_hsa_circ_378669,RMVar_hsa_circ_143833,RMVar_hsa_circ_143831 22171 RMVar_ID_22171 Human_SNP_ID_436466055 A-to-I Human chr10 - 68489053 68489053 68489053 GTTTGTCAGGCTGATCTCGAACGCCTGACCTCAGGTAATCCGCCCACCTCAGCCTCCCAAATTGT GTTTGTCAGGCTGATCTCGAACGCCTGACCTCGGGTAATCCGCCCACCTCAGCCTCCCAAATTGT T C SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs371744502 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_143830,RMVar_hsa_circ_143828,RMVar_hsa_circ_143829,RMVar_hsa_circ_143832,RMVar_hsa_circ_269316,RMVar_hsa_circ_269457,RMVar_hsa_circ_378669,RMVar_hsa_circ_143831,RMVar_hsa_circ_143841,RMVar_hsa_circ_274355,RMVar_hsa_circ_275037,RMVar_hsa_circ_286829,RMVar_hsa_circ_336051,RMVar_hsa_circ_275322,RMVar_hsa_circ_274505,RMVar_hsa_circ_104819,RMVar_hsa_circ_143843,RMVar_hsa_circ_143844,RMVar_hsa_circ_143842,RMVar_hsa_circ_143837,RMVar_hsa_circ_143839,RMVar_hsa_circ_143840,RMVar_hsa_circ_143838,RMVar_hsa_circ_143845,RMVar_hsa_circ_273279,RMVar_hsa_circ_343849,RMVar_hsa_circ_143846 22172 RMVar_ID_22172 Human_SNP_ID_436466056 A-to-I Human chr10 - 68489053 68489053 68489053 GTTTGTCAGGCTGATCTCGAACGCCTGACCTCAGGTAATCCGCCCACCTCAGCCTCCCAAATTGT GTTTGTCAGGCTGATCTCGAACGCCTGACCTCCGGTAATCCGCCCACCTCAGCCTCCCAAATTGT T G SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs371744502 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_143830,RMVar_hsa_circ_143828,RMVar_hsa_circ_143829,RMVar_hsa_circ_143832,RMVar_hsa_circ_269316,RMVar_hsa_circ_269457,RMVar_hsa_circ_378669,RMVar_hsa_circ_143831,RMVar_hsa_circ_143841,RMVar_hsa_circ_274355,RMVar_hsa_circ_275037,RMVar_hsa_circ_286829,RMVar_hsa_circ_336051,RMVar_hsa_circ_275322,RMVar_hsa_circ_274505,RMVar_hsa_circ_104819,RMVar_hsa_circ_143843,RMVar_hsa_circ_143844,RMVar_hsa_circ_143842,RMVar_hsa_circ_143837,RMVar_hsa_circ_143839,RMVar_hsa_circ_143840,RMVar_hsa_circ_143838,RMVar_hsa_circ_143845,RMVar_hsa_circ_273279,RMVar_hsa_circ_343849,RMVar_hsa_circ_143846 22173 RMVar_ID_22173 Human_SNP_ID_436468415 A-to-I Human chr10 - 68497992 68497992 68497992 CTCACTCTATAAACCCAGTTCTTTGGGAGGCTAAGGAGGGAGGATTGCTTGAGCCCAGGAATTCA CTCACTCTATAAACCCAGTTCTTTGGGAGGCTGAGGAGGGAGGATTGCTTGAGCCCAGGAATTCA T C SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1449764944 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24825123 RMVar_hsa_circ_14948,RMVar_hsa_circ_143830,RMVar_hsa_circ_143829,RMVar_hsa_circ_269316,RMVar_hsa_circ_143831,RMVar_hsa_circ_143841,RMVar_hsa_circ_275037,RMVar_hsa_circ_286829,RMVar_hsa_circ_336051,RMVar_hsa_circ_275322,RMVar_hsa_circ_274505,RMVar_hsa_circ_143843,RMVar_hsa_circ_143844,RMVar_hsa_circ_143842,RMVar_hsa_circ_143839,RMVar_hsa_circ_143840,RMVar_hsa_circ_143845,RMVar_hsa_circ_343849,RMVar_hsa_circ_356325,RMVar_hsa_circ_373898,RMVar_hsa_circ_70701,RMVar_hsa_circ_143848 22174 RMVar_ID_22174 Human_SNP_ID_436469038 A-to-I Human chr10 - 68500750 68500750 68500750 TTTTTGGATTTTTAGTAGAGATGGGGGTTTCAATATGTTGGCCAGGCTGGTCTCAAACTCCGGAC TTTTTGGATTTTTAGTAGAGATGGGGGTTTCAGTATGTTGGCCAGGCTGGTCTCAAACTCCGGAC T C SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1273111757 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14948,RMVar_hsa_circ_143830,RMVar_hsa_circ_143829,RMVar_hsa_circ_269316,RMVar_hsa_circ_143831,RMVar_hsa_circ_143841,RMVar_hsa_circ_275037,RMVar_hsa_circ_286829,RMVar_hsa_circ_336051,RMVar_hsa_circ_275322,RMVar_hsa_circ_274505,RMVar_hsa_circ_143843,RMVar_hsa_circ_143844,RMVar_hsa_circ_143842,RMVar_hsa_circ_143839,RMVar_hsa_circ_143840,RMVar_hsa_circ_143845,RMVar_hsa_circ_343849,RMVar_hsa_circ_356325,RMVar_hsa_circ_373898,RMVar_hsa_circ_70701,RMVar_hsa_circ_143848 22175 RMVar_ID_22175 Human_SNP_ID_436469039 A-to-I Human chr10 - 68500750 68500750 68500750 TTTTTGGATTTTTAGTAGAGATGGGGGTTTCAATATGTTGGCCAGGCTGGTCTCAAACTCCGGAC TTTTTGGATTTTTAGTAGAGATGGGGGTTTCACTATGTTGGCCAGGCTGGTCTCAAACTCCGGAC T G SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1273111757 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14948,RMVar_hsa_circ_143830,RMVar_hsa_circ_143829,RMVar_hsa_circ_269316,RMVar_hsa_circ_143831,RMVar_hsa_circ_143841,RMVar_hsa_circ_275037,RMVar_hsa_circ_286829,RMVar_hsa_circ_336051,RMVar_hsa_circ_275322,RMVar_hsa_circ_274505,RMVar_hsa_circ_143843,RMVar_hsa_circ_143844,RMVar_hsa_circ_143842,RMVar_hsa_circ_143839,RMVar_hsa_circ_143840,RMVar_hsa_circ_143845,RMVar_hsa_circ_343849,RMVar_hsa_circ_356325,RMVar_hsa_circ_373898,RMVar_hsa_circ_70701,RMVar_hsa_circ_143848 22176 RMVar_ID_22176 Human_SNP_ID_436469046 A-to-I Human chr10 - 68500769 68500769 68500769 GTGCCACATACCTGGCTAATTTTTGGATTTTTAGTAGAGATGGGGGTTTCAATATGTTGGCCAGG GTGCCACATACCTGGCTAATTTTTGGATTTTTGGTAGAGATGGGGGTTTCAATATGTTGGCCAGG T C SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1398447592 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14948,RMVar_hsa_circ_143830,RMVar_hsa_circ_143829,RMVar_hsa_circ_269316,RMVar_hsa_circ_143831,RMVar_hsa_circ_143841,RMVar_hsa_circ_275037,RMVar_hsa_circ_286829,RMVar_hsa_circ_336051,RMVar_hsa_circ_275322,RMVar_hsa_circ_274505,RMVar_hsa_circ_143843,RMVar_hsa_circ_143844,RMVar_hsa_circ_143842,RMVar_hsa_circ_143839,RMVar_hsa_circ_143840,RMVar_hsa_circ_143845,RMVar_hsa_circ_343849,RMVar_hsa_circ_356325,RMVar_hsa_circ_373898,RMVar_hsa_circ_70701,RMVar_hsa_circ_143848 22177 RMVar_ID_22177 Human_SNP_ID_436471177 A-to-I Human chr10 - 68508521 68508521 68508521 TAGTAGAGACGGGAGTTTCTCCATGTTGGTCAAGCTGGTCTCGAACTCCCAACCTTAGGTGATCC TAGTAGAGACGGGAGTTTCTCCATGTTGGTCAGGCTGGTCTCGAACTCCCAACCTTAGGTGATCC T C SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs901312338 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14948,RMVar_hsa_circ_143830,RMVar_hsa_circ_336051,RMVar_hsa_circ_275322,RMVar_hsa_circ_274505,RMVar_hsa_circ_143843,RMVar_hsa_circ_143844,RMVar_hsa_circ_143842,RMVar_hsa_circ_70701,RMVar_hsa_circ_35445,RMVar_hsa_circ_63329 22178 RMVar_ID_22178 Human_SNP_ID_436472526 A-to-I Human chr10 - 68512939 68512939 68512939 CGCCTCCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCTAGTGGCTGGGATTACGGGCACCCG CGCCTCCCAGGTTCAAGCAATTCTCCTGCCTCGGCCTCCCTAGTGGCTGGGATTACGGGCACCCG T C SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1187804602 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14948,RMVar_hsa_circ_143830,RMVar_hsa_circ_336051,RMVar_hsa_circ_275322,RMVar_hsa_circ_274505,RMVar_hsa_circ_143843,RMVar_hsa_circ_143844,RMVar_hsa_circ_143842,RMVar_hsa_circ_70701,RMVar_hsa_circ_35445,RMVar_hsa_circ_63329 22179 RMVar_ID_22179 Human_SNP_ID_436473051 A-to-I Human chr10 - 68514841 68514841 68514841 CCTAGTTACTCGGGAGATTGAGGCAGGAGAATAGCTTGAATCTGGGAGGTGGAGGTTGCTGTAAG CCTAGTTACTCGGGAGATTGAGGCAGGAGAATTGCTTGAATCTGGGAGGTGGAGGTTGCTGTAAG T A SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1406694999 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14948,RMVar_hsa_circ_143830,RMVar_hsa_circ_336051,RMVar_hsa_circ_275322,RMVar_hsa_circ_274505,RMVar_hsa_circ_143843,RMVar_hsa_circ_143844,RMVar_hsa_circ_143842,RMVar_hsa_circ_70701,RMVar_hsa_circ_35445,RMVar_hsa_circ_63329 22180 RMVar_ID_22180 Human_SNP_ID_436473101 A-to-I Human chr10 - 68515027 68515027 68515027 AAAAAAAAAAATCAAGACTTTAGGCCAGGTGCAGTGGCTCATGCCTGTATTCCCAGTACTTTGGG AAAAAAAAAAATCAAGACTTTAGGCCAGGTGCGGTGGCTCATGCCTGTATTCCCAGTACTTTGGG T C SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1221993948 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14948,RMVar_hsa_circ_143830,RMVar_hsa_circ_336051,RMVar_hsa_circ_275322,RMVar_hsa_circ_274505,RMVar_hsa_circ_143843,RMVar_hsa_circ_143844,RMVar_hsa_circ_143842,RMVar_hsa_circ_70701,RMVar_hsa_circ_35445,RMVar_hsa_circ_63329 22181 RMVar_ID_22181 Human_SNP_ID_436473721 A-to-I Human chr10 - 68517472 68517472 68517472 ATTACTAGATGTACAGTATTGTAGAGAAGTCTATATTATTGCTTTAGAAGCATGCCAAGCTCGAA ATTACTAGATGTACAGTATTGTAGAGAAGTCTGTATTATTGCTTTAGAAGCATGCCAAGCTCGAA T C SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs553247416 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1769286,Human_RBP_ID_9603591,Human_RBP_ID_11399782,Human_RBP_ID_24825220,Human_RBP_ID_26880824 22182 RMVar_ID_22182 Human_SNP_ID_436473762 A-to-I Human chr10 - 68517621 68517621 68517621 CACTGTGTTTCCCAGGCTGGTCTCAAACTCCTAGTCTCAAGTAATTTTTCTACCTCAGCCTCCGA CACTGTGTTTCCCAGGCTGGTCTCAAACTCCTCGTCTCAAGTAATTTTTCTACCTCAGCCTCCGA T G SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE38233;GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,32596459 RNA-Seq:(High) rs1194225417 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5990366,Human_RBP_ID_9623229,Human_RBP_ID_11399798,Human_RBP_ID_22883577 22183 RMVar_ID_22183 Human_SNP_ID_436474058 A-to-I Human chr10 - 68518688 68518687 68518689 CTCACTATTACCTCTGCCTCCTGGGTTCATGCAATTCTTCTGCCTCAGCCTCCCAAGCAGCTGGG CTCACTATTACCTCTGCCTCCTGGGTTCATG__ATTCTTCTGCCTCAGCCTCCCAAGCAGCTGGG TTG T SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE123020:GSM3490829,GSM3490830,GSM3490831 esophageal squamous carcinoma cells,EC109 cell line - 32596459 RNA-Seq:(High) rs1412518859 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_11399844 22184 RMVar_ID_22184 Human_SNP_ID_436474062 A-to-I Human chr10 - 68518692 68518692 68518692 TCGGCTCACTATTACCTCTGCCTCCTGGGTTCATGCAATTCTTCTGCCTCAGCCTCCCAAGCAGC TCGGCTCACTATTACCTCTGCCTCCTGGGTTCGTGCAATTCTTCTGCCTCAGCCTCCCAAGCAGC T C SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991553403 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11399844 22185 RMVar_ID_22185 Human_SNP_ID_436474308 A-to-I Human chr10 - 68519404 68519404 68519404 TCAGCTCACTGAGACCTCTGCCTCCCGGGTTCAGGCAATTCTCTGCCTCAGCCTCCCGAGTAGCT TCAGCTCACTGAGACCTCTGCCTCCCGGGTTCGGGCAATTCTCTGCCTCAGCCTCCCGAGTAGCT T C SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985515138 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11399860 22186 RMVar_ID_22186 Human_SNP_ID_436474320 A-to-I Human chr10 - 68519434 68519434 68519434 TCACCCAGGCTGGAGTGCAGTGGCACAATCTCAGCTCACTGAGACCTCTGCCTCCCGGGTTCAGG TCACCCAGGCTGGAGTGCAGTGGCACAATCTCGGCTCACTGAGACCTCTGCCTCCCGGGTTCAGG T C SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1481866588 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11399860 22187 RMVar_ID_22187 Human_SNP_ID_436474401 A-to-I Human chr10 - 68519832 68519832 68519832 CGGCTCACTGCCACCTATGCCTCCCGGGTTCAAGCGATTCTCCTGCCCCAGCTTTCCAAGTATCT CGGCTCACTGCCACCTATGCCTCCCGGGTTCAGGCGATTCTCCTGCCCCAGCTTTCCAAGTATCT T C SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1190956655 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11399872 22188 RMVar_ID_22188 Human_SNP_ID_436474488 A-to-I Human chr10 - 68520062 68520062 68520062 CCTGTAATCCCACCTACTCGGGAGGCTGGGGCAGGAGAATCGCTTGAACCTGGGAGGTGAAGGTT CCTGTAATCCCACCTACTCGGGAGGCTGGGGCCGGAGAATCGCTTGAACCTGGGAGGTGAAGGTT T G SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1341776966 Functional Loss SNV dbSNP153 33..33 33 - - - 22189 RMVar_ID_22189 Human_SNP_ID_436474510 A-to-I Human chr10 - 68520152 68520151 68520152 GAGTTCAAGAACAGTCTGGCCAACATGGTGAAACCCTCTCTCTACTAAAGACTAAAAAAAGAAAA GAGTTCAAGAACAGTCTGGCCAACATGGTGAA_CCCTCTCTCTACTAAAGACTAAAAAAAGAAAA GT G SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs889933581 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_11399876,Human_RBP_ID_17558992 22190 RMVar_ID_22190 Human_SNP_ID_436474580 A-to-I Human chr10 - 68520430 68520430 68520430 CTCAAGTGATCCTCCCACCTAGGCCTCCCAAAATGCTGGGATTATAGGCATGAGCCATTGTGCCC CTCAAGTGATCCTCCCACCTAGGCCTCCCAAAGTGCTGGGATTATAGGCATGAGCCATTGTGCCC T C SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2488042 Functional Loss SNV dbSNP153 33..33 33 - - - 22191 RMVar_ID_22191 Human_SNP_ID_436474665 A-to-I Human chr10 - 68520726 68520726 68520726 ATCACTGCAACCTCTGCCTCCTGGATTCAAGCAATTCTCCTGCCTCAGCCTCCCGTGTAGCTGGG ATCACTGCAACCTCTGCCTCCTGGATTCAAGCGATTCTCCTGCCTCAGCCTCCCGTGTAGCTGGG T C SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1324844478 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24825288 22192 RMVar_ID_22192 Human_SNP_ID_436474763 A-to-I Human chr10 - 68520971 68520971 68520971 TGCCACCATGCCGGCTAATTTTTTGTAGTTTTAGTGGAGACGGGGTTTCACCATGTTAGCCAGGA TGCCACCATGCCGGCTAATTTTTTGTAGTTTTGGTGGAGACGGGGTTTCACCATGTTAGCCAGGA T C SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1447208774 Functional Loss SNV dbSNP153 33..33 33 - - - 22193 RMVar_ID_22193 Human_SNP_ID_436474855 A-to-I Human chr10 - 68521282 68521282 68521282 CTCCTGCCTCAGCCCACCAAAGTGCTGGGATTACAGGCATTAACCACCACAGCCGGCCGGTTTTA CTCCTGCCTCAGCCCACCAAAGTGCTGGGATTTCAGGCATTAACCACCACAGCCGGCCGGTTTTA T A SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1379637179 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24825293 22194 RMVar_ID_22194 Human_SNP_ID_436474856 A-to-I Human chr10 - 68521282 68521282 68521282 CTCCTGCCTCAGCCCACCAAAGTGCTGGGATTACAGGCATTAACCACCACAGCCGGCCGGTTTTA CTCCTGCCTCAGCCCACCAAAGTGCTGGGATTGCAGGCATTAACCACCACAGCCGGCCGGTTTTA T C SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1379637179 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24825293 22195 RMVar_ID_22195 Human_SNP_ID_436474864 A-to-I Human chr10 - 68521344 68521344 68521344 GTTAGTAGAGATGGGGTTTTGCCATGTTGGCCAGGCTGGTCTCGAACTGAGCTCAAGTGATCCTC GTTAGTAGAGATGGGGTTTTGCCATGTTGGCCGGGCTGGTCTCGAACTGAGCTCAAGTGATCCTC T C SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941915015 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225802,Human_RBP_ID_22470851 22196 RMVar_ID_22196 Human_SNP_ID_436474865 A-to-I Human chr10 - 68521344 68521344 68521344 GTTAGTAGAGATGGGGTTTTGCCATGTTGGCCAGGCTGGTCTCGAACTGAGCTCAAGTGATCCTC GTTAGTAGAGATGGGGTTTTGCCATGTTGGCCCGGCTGGTCTCGAACTGAGCTCAAGTGATCCTC T G SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941915015 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225802,Human_RBP_ID_22470851 22197 RMVar_ID_22197 Human_SNP_ID_436474882 A-to-I Human chr10 - 68521434 68521434 68521434 ACATCCGCTTCTTGGGTTCAAGCGATTCTGCCACCTCAGACTCCACAGTAGTTGGGATTACAGGT ACATCCGCTTCTTGGGTTCAAGCGATTCTGCCGCCTCAGACTCCACAGTAGTTGGGATTACAGGT T C SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE38233;GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,32596459 RNA-Seq:(High) rs1247782947 Functional Loss SNV dbSNP153 33..33 33 - - - 22198 RMVar_ID_22198 Human_SNP_ID_436475097 A-to-I Human chr10 - 68522062 68522062 68522062 GGCTCCCGAGTTCAAGCGATTTTACCGCCTCAACCTCCCGATTAGCTGGGACTACAGGTGGTGTG GGCTCCCGAGTTCAAGCGATTTTACCGCCTCAGCCTCCCGATTAGCTGGGACTACAGGTGGTGTG T C SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1379388758 Functional Loss SNV dbSNP153 33..33 33 - - - 22199 RMVar_ID_22199 Human_SNP_ID_436475107 A-to-I Human chr10 - 68522137 68522137 68522137 TTTTTTTGAGACAGAGTCTCTCTCTGTTGTCCAGGCTGGAGTGCAGCAGCATGATCTCAGCTCAC TTTTTTTGAGACAGAGTCTCTCTCTGTTGTCCTGGCTGGAGTGCAGCAGCATGATCTCAGCTCAC T A SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7084085 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17558993 GWAS_ID_2001,GWAS_ID_2002,GWAS_ID_2003,GWAS_ID_2004,GWAS_ID_2005,GWAS_ID_2006,GWAS_ID_2007,GWAS_ID_2008,GWAS_ID_2009,GWAS_ID_2010,GWAS_ID_2011,GWAS_ID_2012,GWAS_ID_2013,GWAS_ID_2014 22200 RMVar_ID_22200 Human_SNP_ID_436475108 A-to-I Human chr10 - 68522137 68522137 68522137 TTTTTTTGAGACAGAGTCTCTCTCTGTTGTCCAGGCTGGAGTGCAGCAGCATGATCTCAGCTCAC TTTTTTTGAGACAGAGTCTCTCTCTGTTGTCCGGGCTGGAGTGCAGCAGCATGATCTCAGCTCAC T C SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7084085 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17558993 GWAS_ID_2001,GWAS_ID_2002,GWAS_ID_2003,GWAS_ID_2004,GWAS_ID_2005,GWAS_ID_2006,GWAS_ID_2007,GWAS_ID_2008,GWAS_ID_2009,GWAS_ID_2010,GWAS_ID_2011,GWAS_ID_2012,GWAS_ID_2013,GWAS_ID_2014 22201 RMVar_ID_22201 Human_SNP_ID_436475118 A-to-I Human chr10 - 68522157 68522157 68522157 TTCTTTTCTTTTTTCTTTTTTTTTTTTGAGACAGAGTCTCTCTCTGTTGTCCAGGCTGGAGTGCA TTCTTTTCTTTTTTCTTTTTTTTTTTTGAGACGGAGTCTCTCTCTGTTGTCCAGGCTGGAGTGCA T C SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1322118477 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11399947,Human_RBP_ID_17558993 22202 RMVar_ID_22202 Human_SNP_ID_436475189 A-to-I Human chr10 - 68522463 68522463 68522463 TCTGGCCAGACTGGTCTCGAATTCCTGACCTTAAGTGATCCACCTGCCTTGGCCTCCCAATGTGT TCTGGCCAGACTGGTCTCGAATTCCTGACCTTGAGTGATCCACCTGCCTTGGCCTCCCAATGTGT T C SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs981638387 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11399963,Human_RBP_ID_22470598,Human_RBP_ID_24859859 22203 RMVar_ID_22203 Human_SNP_ID_436475195 A-to-I Human chr10 - 68522486 68522486 68522486 CAGTGGAGACCGGGTTTCACCATTCTGGCCAGACTGGTCTCGAATTCCTGACCTTAAGTGATCCA CAGTGGAGACCGGGTTTCACCATTCTGGCCAGCCTGGTCTCGAATTCCTGACCTTAAGTGATCCA T G SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1284414571 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11399963,Human_RBP_ID_17558803,Human_RBP_ID_22470598 22204 RMVar_ID_22204 Human_SNP_ID_436475243 A-to-I Human chr10 - 68522666 68522666 68522666 GGACTATAGGCGTGTGTCACCACACCTGGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCA GGACTATAGGCGTGTGTCACCACACCTGGCTAGTTTTTTGTATTTTTAGTAGAGACGGGGTTTCA T C SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1246578412 Functional Loss SNV dbSNP153 33..33 33 - - - 22205 RMVar_ID_22205 Human_SNP_ID_436475271 A-to-I Human chr10 - 68522777 68522777 68522777 GGAATCTCACTCTGTTGCCTAGGCTAGAGTGCAGTGGTGCAATCTTGGCTCACTACAACCTCCAG GGAATCTCACTCTGTTGCCTAGGCTAGAGTGCGGTGGTGCAATCTTGGCTCACTACAACCTCCAG T C SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs920602368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11399969,Human_RBP_ID_22154691,Human_RBP_ID_23152439 22206 RMVar_ID_22206 Human_SNP_ID_436475378 A-to-I Human chr10 - 68523150 68523150 68523150 GAGAGGCGGAGGTCGCAGTAAGCCCAGATCGCAGCACTGCACTCAAGCCTGAGCAACAGAGCCAG GAGAGGCGGAGGTCGCAGTAAGCCCAGATCGCTGCACTGCACTCAAGCCTGAGCAACAGAGCCAG T A SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947806528 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5990417,Human_RBP_ID_11399988,Human_RBP_ID_23152446 22207 RMVar_ID_22207 Human_SNP_ID_436475384 A-to-I Human chr10 - 68523166 68523166 68523166 AGAATCACTTGAACGCGAGAGGCGGAGGTCGCAGTAAGCCCAGATCGCAGCACTGCACTCAAGCC AGAATCACTTGAACGCGAGAGGCGGAGGTCGCGGTAAGCCCAGATCGCAGCACTGCACTCAAGCC T C SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1045410453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11399988,Human_RBP_ID_23152447 22208 RMVar_ID_22208 Human_SNP_ID_436475385 A-to-I Human chr10 - 68523166 68523166 68523166 AGAATCACTTGAACGCGAGAGGCGGAGGTCGCAGTAAGCCCAGATCGCAGCACTGCACTCAAGCC AGAATCACTTGAACGCGAGAGGCGGAGGTCGCCGTAAGCCCAGATCGCAGCACTGCACTCAAGCC T G SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1045410453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11399988,Human_RBP_ID_23152447 22209 RMVar_ID_22209 Human_SNP_ID_436475399 A-to-I Human chr10 - 68523214 68523214 68523214 GTGGCGCCCACCTGTTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACGCG GTGGCGCCCACCTGTTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACGCG T C SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11816020 Functional Loss SNV dbSNP153 33..33 33 - - - 22210 RMVar_ID_22210 Human_SNP_ID_436475414 A-to-I Human chr10 - 68523257 68523257 68523257 GACACCCAGTCTGTACAAAAAATACAAAAATTAGCTGGGCATGGTGGCGCCCACCTGTTGTAGTC GACACCCAGTCTGTACAAAAAATACAAAAATTGGCTGGGCATGGTGGCGCCCACCTGTTGTAGTC T C SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1312294374 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11399994 22211 RMVar_ID_22211 Human_SNP_ID_436475417 A-to-I Human chr10 - 68523271 68523271 68523271 CTGGGCAACATAGTGACACCCAGTCTGTACAAAAAATACAAAAATTAGCTGGGCATGGTGGCGCC CTGGGCAACATAGTGACACCCAGTCTGTACAACAAATACAAAAATTAGCTGGGCATGGTGGCGCC T G SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs761968592 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23152449,Human_RBP_ID_24825327 22212 RMVar_ID_22212 Human_SNP_ID_436475422 A-to-I Human chr10 - 68523292 68523292 68523292 GCTAATGAGTTGGAGACCAGCCTGGGCAACATAGTGACACCCAGTCTGTACAAAAAATACAAAAA GCTAATGAGTTGGAGACCAGCCTGGGCAACATGGTGACACCCAGTCTGTACAAAAAATACAAAAA T C SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10998246 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11399995,Human_RBP_ID_23304633 22213 RMVar_ID_22213 Human_SNP_ID_436475493 A-to-I Human chr10 - 68523540 68523540 68523540 TCAACCTGGGTGGTGGAGGTTGTTGTGAGACAAGATCGCTCCACTGCACTCCAGCCTGGGCAACA TCAACCTGGGTGGTGGAGGTTGTTGTGAGACAGGATCGCTCCACTGCACTCCAGCCTGGGCAACA T C SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs777777795 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11400007,Human_RBP_ID_23152456 22214 RMVar_ID_22214 Human_SNP_ID_436475508 A-to-I Human chr10 - 68523601 68523601 68523601 AGGCTTGGTGGCACGCACCTGTAGTCCCAGCTACTTGGGAAGCTGAGGCATGAGAATCGCTTCAA AGGCTTGGTGGCACGCACCTGTAGTCCCAGCTGCTTGGGAAGCTGAGGCATGAGAATCGCTTCAA T C SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1178469207 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11400008 22215 RMVar_ID_22215 Human_SNP_ID_436475522 A-to-I Human chr10 - 68523668 68523668 68523668 GAGTTCAAGACCATCCCGGCCAACATGGCGAAACCCCATCTCTACTAAAAATACAAAAAAACTAG GAGTTCAAGACCATCCCGGCCAACATGGCGAAGCCCCATCTCTACTAAAAATACAAAAAAACTAG T C SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1339363833 Functional Loss SNV dbSNP153 33..33 33 - - - 22216 RMVar_ID_22216 Human_SNP_ID_436475549 A-to-I Human chr10 - 68523770 68523770 68523770 TTTTGTTCTGCTGATAAAATGACATTTAGGCTAGGTGAGGTGTCTCACACCTGTAATCCCAGCAC TTTTGTTCTGCTGATAAAATGACATTTAGGCTTGGTGAGGTGTCTCACACCTGTAATCCCAGCAC T A SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1356594213 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11400014 22217 RMVar_ID_22217 Human_SNP_ID_436475585 A-to-I Human chr10 - 68523944 68523944 68523944 GGCGTGAGCCACTGTGCCTGGCCCTAATTTTTATATTTTTAGCAGAGACAGGGTTTTACCATGTT GGCGTGAGCCACTGTGCCTGGCCCTAATTTTTGTATTTTTAGCAGAGACAGGGTTTTACCATGTT T C SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs990631673 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24825341,Human_RBP_ID_26880831 22218 RMVar_ID_22218 Human_SNP_ID_436475626 A-to-I Human chr10 - 68524066 68524066 68524066 GACCTCGTGATCCGCCCGCCTTGACCTCCCATAGTGCTGGGATTACAGGCGTGAGCCACCTGGTC GACCTCGTGATCCGCCCGCCTTGACCTCCCATGGTGCTGGGATTACAGGCGTGAGCCACCTGGTC T C SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1353202241 Functional Loss SNV dbSNP153 33..33 33 - - - 22219 RMVar_ID_22219 Human_SNP_ID_436475805 A-to-I Human chr10 - 68524376 68524376 68524376 CCACCACACCCAGCTAATTTTGTATTTTTAGTAGAGACGAAGTTTTACCATGTTGGCCAGGATGG CCACCACACCCAGCTAATTTTGTATTTTTAGTGGAGACGAAGTTTTACCATGTTGGCCAGGATGG T C SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1269943069 Functional Loss SNV dbSNP153 33..33 33 - - - 22220 RMVar_ID_22220 Human_SNP_ID_436475814 A-to-I Human chr10 - 68524401 68524401 68524401 GAGTAGCTAGGACTATAGGTGTGTGCCACCACACCCAGCTAATTTTGTATTTTTAGTAGAGACGA GAGTAGCTAGGACTATAGGTGTGTGCCACCACGCCCAGCTAATTTTGTATTTTTAGTAGAGACGA T C SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1420247821 Functional Loss SNV dbSNP153 33..33 33 - - - 22221 RMVar_ID_22221 Human_SNP_ID_436475828 A-to-I Human chr10 - 68524425 68524425 68524425 GAGATTCTCCTGCCTCAGCTTCCTGAGTAGCTAGGACTATAGGTGTGTGCCACCACACCCAGCTA GAGATTCTCCTGCCTCAGCTTCCTGAGTAGCTGGGACTATAGGTGTGTGCCACCACACCCAGCTA T C SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1042031922 Functional Loss SNV dbSNP153 33..33 33 - - - 22222 RMVar_ID_22222 Human_SNP_ID_436475839 A-to-I Human chr10 - 68524489 68524489 68524489 TCACCCAGGCTGGAGTGCATTAGTGCCATCTCAGCTCACTGCAACCTTTGCCTCCTGGGTTCAAG TCACCCAGGCTGGAGTGCATTAGTGCCATCTCCGCTCACTGCAACCTTTGCCTCCTGGGTTCAAG T G SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1213389162 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9603620,Human_RBP_ID_24825352 22223 RMVar_ID_22223 Human_SNP_ID_436475852 A-to-I Human chr10 - 68524544 68524540 68524544 CCACCGTGCCTGGCTAATTTATTTATTTATTTATTTTTGAGACGGTGTCTTACTCTCACCCAGGC CCACCGTGCCTGGCTAATTTATTTATTTATTT____TTGAGACGGTGTCTTACTCTCACCCAGGC AAAAT A SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1242948427 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_6033222,Human_RBP_ID_11400031,Human_RBP_ID_24859868 22224 RMVar_ID_22224 Human_SNP_ID_436475873 A-to-I Human chr10 - 68524627 68524627 68524627 CTCGGCTCACTGCAACCTCTGCCGCCTGGTTCAAGCGATTCTCCTGCCTCAACCTCCCGAGTAGC CTCGGCTCACTGCAACCTCTGCCGCCTGGTTCGAGCGATTCTCCTGCCTCAACCTCCCGAGTAGC T C SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs952204032 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24825354 22225 RMVar_ID_22225 Human_SNP_ID_436475971 A-to-I Human chr10 - 68524839 68524839 68524839 GGAGTCTCACTCTGTCGGCCAGGCTGGAGTGCAGCGGCACGATCTCTGCTCACTGCAACCTCCGT GGAGTCTCACTCTGTCGGCCAGGCTGGAGTGCGGCGGCACGATCTCTGCTCACTGCAACCTCCGT T C SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1008294315 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5990419,Human_RBP_ID_11400039 22226 RMVar_ID_22226 Human_SNP_ID_436476006 A-to-I Human chr10 - 68524985 68524985 68524985 AGGAGTGCAGTGGCGTGATCTTGGCTCACTGCAACCTCTGCTTCCTGGGTTCAAGTGATTCTGCT AGGAGTGCAGTGGCGTGATCTTGGCTCACTGCGACCTCTGCTTCCTGGGTTCAAGTGATTCTGCT T C SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs745405267 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11400045 22227 RMVar_ID_22227 Human_SNP_ID_436476014 A-to-I Human chr10 - 68525009 68525009 68525009 AGAGTCTCACTCCCTCACCCAGGCAGGAGTGCAGTGGCGTGATCTTGGCTCACTGCAACCTCTGC AGAGTCTCACTCCCTCACCCAGGCAGGAGTGCGGTGGCGTGATCTTGGCTCACTGCAACCTCTGC T C SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs967128538 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11485050,Human_RBP_ID_17559446,Human_RBP_ID_23152471 22228 RMVar_ID_22228 Human_SNP_ID_436476068 A-to-I Human chr10 - 68525260 68525260 68525260 GTGGTGGCACTCGCCTGTAATCCCAGCTACTCAGGAGGCTTAAGGCAGGAGAGTCGCCTAAATCA GTGGTGGCACTCGCCTGTAATCCCAGCTACTCTGGAGGCTTAAGGCAGGAGAGTCGCCTAAATCA T A SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1230600729 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11400059 22229 RMVar_ID_22229 Human_SNP_ID_436476070 A-to-I Human chr10 - 68525273 68525266 68525273 AAATTTGTCAGGCGTGGTGGCACTCGCCTGTAATCCCAGCTACTCAGGAGGCTTAAGGCAGGAGA AAATTTGTCAGGCGTGGTGGCACTCGCCTGTA_______CTACTCAGGAGGCTTAAGGCAGGAGA GCTGGGAT G SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1243453606 Functional Loss DEL dbSNP153 33..39 33 - - - Human_RBP_ID_23152478 22230 RMVar_ID_22230 Human_SNP_ID_436476075 A-to-I Human chr10 - 68525284 68525284 68525284 TAAAACTACAAAAATTTGTCAGGCGTGGTGGCACTCGCCTGTAATCCCAGCTACTCAGGAGGCTT TAAAACTACAAAAATTTGTCAGGCGTGGTGGCGCTCGCCTGTAATCCCAGCTACTCAGGAGGCTT T C SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1428791666 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11400060 22231 RMVar_ID_22231 Human_SNP_ID_436476155 A-to-I Human chr10 - 68525516 68525516 68525516 CCAGGAGATCGAGGCTCCAGTAAGCCATGATCACACCACTACCCTCCAGCCTGAGCTACAGAGAG CCAGGAGATCGAGGCTCCAGTAAGCCATGATCGCACCACTACCCTCCAGCCTGAGCTACAGAGAG T C SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1019952660 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9623239 22232 RMVar_ID_22232 Human_SNP_ID_436476169 A-to-I Human chr10 - 68525565 68525565 68525565 ACTGTAGTCCCAGTTACTAGGGAAGCTGAGGCAGGAAGACTGCTTGAGTCCAGGAGATCGAGGCT ACTGTAGTCCCAGTTACTAGGGAAGCTGAGGCGGGAAGACTGCTTGAGTCCAGGAGATCGAGGCT T C SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs931075112 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5990420 22233 RMVar_ID_22233 Human_SNP_ID_436476172 A-to-I Human chr10 - 68525592 68525592 68525592 CATTGAAGTTGTGTGCAGTGGCTCACTACTGTAGTCCCAGTTACTAGGGAAGCTGAGGCAGGAAG CATTGAAGTTGTGTGCAGTGGCTCACTACTGTGGTCCCAGTTACTAGGGAAGCTGAGGCAGGAAG T C SLC25A16 Ensembl:ENSG00000122912 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1138830 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11400065,Human_RBP_ID_24825378 22234 RMVar_ID_22234 Human_SNP_ID_436481392 A-to-I Human chr10 + 68544528 68544528 68544528 GATGTCATCAACATACGAACTCCAACTTTGGCAGCCATCAGCAAACTGGCACCTGCAATTAAACC GATGTCATCAACATACGAACTCCAACTTTGGCGGCCATCAGCAAACTGGCACCTGCAATTAAACC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878858980 Functional Loss SNV dbSNP153 33..33 33 - - - 22235 RMVar_ID_22235 Human_SNP_ID_436529444 A-to-I Human chr10 + 68724090 68724090 68724090 TGAAGCTGGAGAATCGCTTGAACGTGGGAGGCAGAGGTTACAGTGAGCCGAGATCACACCACCGC TGAAGCTGGAGAATCGCTTGAACGTGGGAGGCGGAGGTTACAGTGAGCCGAGATCACACCACCGC A G CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1240992431 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14730,RMVar_hsa_circ_333610,RMVar_hsa_circ_115362,RMVar_hsa_circ_356781,RMVar_hsa_circ_368562,RMVar_hsa_circ_143879,RMVar_hsa_circ_367534,RMVar_hsa_circ_342893,RMVar_hsa_circ_305184,RMVar_hsa_circ_307164,RMVar_hsa_circ_308263,RMVar_hsa_circ_306748,RMVar_hsa_circ_37797,RMVar_hsa_circ_69904,RMVar_hsa_circ_20502,RMVar_hsa_circ_143881,RMVar_hsa_circ_562,RMVar_hsa_circ_1627,RMVar_hsa_circ_143882,RMVar_hsa_circ_143883,RMVar_hsa_circ_143880 22236 RMVar_ID_22236 Human_SNP_ID_436530263 A-to-I Human chr10 + 68726875 68726875 68726875 AAAATTAGCCGGACATAGTGGTGTGCATCTGTAATCCCAGCTATTCGGGAGGCTGAGGCAGGAGA AAAATTAGCCGGACATAGTGGTGTGCATCTGTTATCCCAGCTATTCGGGAGGCTGAGGCAGGAGA A T CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1384833889 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14730,RMVar_hsa_circ_333610,RMVar_hsa_circ_115362,RMVar_hsa_circ_356781,RMVar_hsa_circ_368562,RMVar_hsa_circ_143879,RMVar_hsa_circ_367534,RMVar_hsa_circ_342893,RMVar_hsa_circ_305184,RMVar_hsa_circ_307164,RMVar_hsa_circ_308263,RMVar_hsa_circ_306748,RMVar_hsa_circ_37797,RMVar_hsa_circ_69904,RMVar_hsa_circ_20502,RMVar_hsa_circ_143881,RMVar_hsa_circ_562,RMVar_hsa_circ_1627,RMVar_hsa_circ_143882,RMVar_hsa_circ_143883,RMVar_hsa_circ_143880 22237 RMVar_ID_22237 Human_SNP_ID_436530751 A-to-I Human chr10 + 68728778 68728778 68728778 GGAGTTTGAGACCCACCCACCTAACCTGGTGAAACCCTGCCTCTACTAAAAATACAAAAATAAGC GGAGTTTGAGACCCACCCACCTAACCTGGTGAGACCCTGCCTCTACTAAAAATACAAAAATAAGC A G CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1019965042 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14730,RMVar_hsa_circ_333610,RMVar_hsa_circ_115362,RMVar_hsa_circ_356781,RMVar_hsa_circ_368562,RMVar_hsa_circ_143879,RMVar_hsa_circ_367534,RMVar_hsa_circ_342893,RMVar_hsa_circ_305184,RMVar_hsa_circ_307164,RMVar_hsa_circ_308263,RMVar_hsa_circ_306748,RMVar_hsa_circ_37797,RMVar_hsa_circ_69904,RMVar_hsa_circ_20502,RMVar_hsa_circ_143881,RMVar_hsa_circ_562,RMVar_hsa_circ_1627,RMVar_hsa_circ_143882,RMVar_hsa_circ_143883,RMVar_hsa_circ_143880 22238 RMVar_ID_22238 Human_SNP_ID_436531809 A-to-I Human chr10 + 68732405 68732405 68732405 AGAGTCTTGCTCTGTCACCCAGGCTGTAGTGCAGTGGCGCCATCTCAGCTCACCGCAACCTCTGC AGAGTCTTGCTCTGTCACCCAGGCTGTAGTGCGGTGGCGCCATCTCAGCTCACCGCAACCTCTGC A G CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs968898070 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11400722 RMVar_hsa_circ_14730,RMVar_hsa_circ_333610,RMVar_hsa_circ_115362,RMVar_hsa_circ_356781,RMVar_hsa_circ_368562,RMVar_hsa_circ_143879,RMVar_hsa_circ_367534,RMVar_hsa_circ_342893,RMVar_hsa_circ_305184,RMVar_hsa_circ_307164,RMVar_hsa_circ_308263,RMVar_hsa_circ_306748,RMVar_hsa_circ_37797,RMVar_hsa_circ_69904,RMVar_hsa_circ_20502,RMVar_hsa_circ_143881,RMVar_hsa_circ_562,RMVar_hsa_circ_1627,RMVar_hsa_circ_143882,RMVar_hsa_circ_143883,RMVar_hsa_circ_143880 22239 RMVar_ID_22239 Human_SNP_ID_436531991 A-to-I Human chr10 + 68733152 68733152 68733152 AGAAAATAGGCCAGGCACAGTGGCTCATACCTATAATCCCAGCACTTTGGGAGGCCGAGGTGGAT AGAAAATAGGCCAGGCACAGTGGCTCATACCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGAT A G CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1268427595 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24825881 RMVar_hsa_circ_14730,RMVar_hsa_circ_333610,RMVar_hsa_circ_115362,RMVar_hsa_circ_356781,RMVar_hsa_circ_368562,RMVar_hsa_circ_143879,RMVar_hsa_circ_367534,RMVar_hsa_circ_342893,RMVar_hsa_circ_305184,RMVar_hsa_circ_307164,RMVar_hsa_circ_308263,RMVar_hsa_circ_306748,RMVar_hsa_circ_37797,RMVar_hsa_circ_69904,RMVar_hsa_circ_20502,RMVar_hsa_circ_143881,RMVar_hsa_circ_562,RMVar_hsa_circ_1627,RMVar_hsa_circ_143882,RMVar_hsa_circ_143883,RMVar_hsa_circ_143880 22240 RMVar_ID_22240 Human_SNP_ID_436533590 A-to-I Human chr10 + 68739205 68739205 68739205 GAGTTTCATTTTTGTTGCCCAGGCTAGAGTGCAATGGTGCGATCTTGGCTCGCTGCAACCTCTGC GAGTTTCATTTTTGTTGCCCAGGCTAGAGTGCGATGGTGCGATCTTGGCTCGCTGCAACCTCTGC A G CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1296943608 Functional Loss SNV dbSNP153 33..33 33 - - - 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_305184,RMVar_hsa_circ_307164,RMVar_hsa_circ_308263,RMVar_hsa_circ_306748,RMVar_hsa_circ_37797,RMVar_hsa_circ_69904,RMVar_hsa_circ_20502,RMVar_hsa_circ_124407,RMVar_hsa_circ_47661,RMVar_hsa_circ_143881,RMVar_hsa_circ_562,RMVar_hsa_circ_1627,RMVar_hsa_circ_143882,RMVar_hsa_circ_143883,RMVar_hsa_circ_321608,RMVar_hsa_circ_344019,RMVar_hsa_circ_118781,RMVar_hsa_circ_289588,RMVar_hsa_circ_67297,RMVar_hsa_circ_143885,RMVar_hsa_circ_143886,RMVar_hsa_circ_143887,RMVar_hsa_circ_290656,RMVar_hsa_circ_337403,RMVar_hsa_circ_326310,RMVar_hsa_circ_282839,RMVar_hsa_circ_143891,RMVar_hsa_circ_107599,RMVar_hsa_circ_115064,RMVar_hsa_circ_143893,RMVar_hsa_circ_63407,RMVar_hsa_circ_143894,RMVar_hsa_circ_143892,RMVar_hsa_circ_143889,RMVar_hsa_circ_143890,RMVar_hsa_circ_143888 22241 RMVar_ID_22241 Human_SNP_ID_436536748 A-to-I Human chr10 + 68750453 68750453 68750453 CATGTTGTTGGCCAGGTTTGTTTCGAACTCCTAACCTCAAGTGATCCACCTGCCTGGCCCTCCCA CATGTTGTTGGCCAGGTTTGTTTCGAACTCCTGACCTCAAGTGATCCACCTGCCTGGCCCTCCCA A G CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1564537748 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11401244 RMVar_hsa_circ_14730,RMVar_hsa_circ_333610,RMVar_hsa_circ_356781,RMVar_hsa_circ_367534,RMVar_hsa_circ_307164,RMVar_hsa_circ_306748,RMVar_hsa_circ_37797,RMVar_hsa_circ_7424,RMVar_hsa_circ_124407,RMVar_hsa_circ_1627,RMVar_hsa_circ_143882,RMVar_hsa_circ_143883,RMVar_hsa_circ_344019,RMVar_hsa_circ_107599,RMVar_hsa_circ_115064,RMVar_hsa_circ_63407,RMVar_hsa_circ_143889,RMVar_hsa_circ_143890,RMVar_hsa_circ_143888,RMVar_hsa_circ_53594,RMVar_hsa_circ_28048,RMVar_hsa_circ_337764,RMVar_hsa_circ_359965,RMVar_hsa_circ_24449,RMVar_hsa_circ_12168,RMVar_hsa_circ_36191,RMVar_hsa_circ_29756,RMVar_hsa_circ_328870,RMVar_hsa_circ_317570,RMVar_hsa_circ_66975,RMVar_hsa_circ_143901 22242 RMVar_ID_22242 Human_SNP_ID_436536928 A-to-I Human chr10 + 68751241 68751241 68751241 TAGAAACAGGGTTTCACCATGTTGGCCAGGCTAATCTCAAACTCCTTACCTCAGGTGATCCAGTC TAGAAACAGGGTTTCACCATGTTGGCCAGGCTCATCTCAAACTCCTTACCTCAGGTGATCCAGTC A C CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1000324355 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14730,RMVar_hsa_circ_333610,RMVar_hsa_circ_356781,RMVar_hsa_circ_367534,RMVar_hsa_circ_307164,RMVar_hsa_circ_306748,RMVar_hsa_circ_37797,RMVar_hsa_circ_7424,RMVar_hsa_circ_124407,RMVar_hsa_circ_1627,RMVar_hsa_circ_143882,RMVar_hsa_circ_143883,RMVar_hsa_circ_344019,RMVar_hsa_circ_107599,RMVar_hsa_circ_115064,RMVar_hsa_circ_63407,RMVar_hsa_circ_143889,RMVar_hsa_circ_143890,RMVar_hsa_circ_143888,RMVar_hsa_circ_53594,RMVar_hsa_circ_28048,RMVar_hsa_circ_337764,RMVar_hsa_circ_359965,RMVar_hsa_circ_24449,RMVar_hsa_circ_12168,RMVar_hsa_circ_36191,RMVar_hsa_circ_29756,RMVar_hsa_circ_328870,RMVar_hsa_circ_317570,RMVar_hsa_circ_66975,RMVar_hsa_circ_143901 22243 RMVar_ID_22243 Human_SNP_ID_436537092 A-to-I Human chr10 + 68751821 68751821 68751821 GGGAGGCAGAGATTGCAGTGTGCCGAGATTGCACCACTGCACTCCAGCCTGGGAGACAGAGGGAG GGGAGGCAGAGATTGCAGTGTGCCGAGATTGCGCCACTGCACTCCAGCCTGGGAGACAGAGGGAG A G CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs564332789 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11401309 RMVar_hsa_circ_14730,RMVar_hsa_circ_333610,RMVar_hsa_circ_356781,RMVar_hsa_circ_367534,RMVar_hsa_circ_307164,RMVar_hsa_circ_306748,RMVar_hsa_circ_37797,RMVar_hsa_circ_7424,RMVar_hsa_circ_124407,RMVar_hsa_circ_1627,RMVar_hsa_circ_143882,RMVar_hsa_circ_143883,RMVar_hsa_circ_344019,RMVar_hsa_circ_107599,RMVar_hsa_circ_115064,RMVar_hsa_circ_63407,RMVar_hsa_circ_143889,RMVar_hsa_circ_143890,RMVar_hsa_circ_143888,RMVar_hsa_circ_53594,RMVar_hsa_circ_28048,RMVar_hsa_circ_337764,RMVar_hsa_circ_359965,RMVar_hsa_circ_24449,RMVar_hsa_circ_12168,RMVar_hsa_circ_36191,RMVar_hsa_circ_29756,RMVar_hsa_circ_328870,RMVar_hsa_circ_317570,RMVar_hsa_circ_66975,RMVar_hsa_circ_143901 22244 RMVar_ID_22244 Human_SNP_ID_436537223 A-to-I Human chr10 + 68752178 68752178 68752178 CTGACCTCATGATCCGCCCACCTCGGCCTCCCAAAGTGCTGGGACTACAGGCGTGAGCCACCGCA CTGACCTCATGATCCGCCCACCTCGGCCTCCCGAAGTGCTGGGACTACAGGCGTGAGCCACCGCA A G CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1477016392 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14730,RMVar_hsa_circ_333610,RMVar_hsa_circ_356781,RMVar_hsa_circ_367534,RMVar_hsa_circ_307164,RMVar_hsa_circ_306748,RMVar_hsa_circ_37797,RMVar_hsa_circ_7424,RMVar_hsa_circ_124407,RMVar_hsa_circ_1627,RMVar_hsa_circ_143882,RMVar_hsa_circ_143883,RMVar_hsa_circ_344019,RMVar_hsa_circ_107599,RMVar_hsa_circ_115064,RMVar_hsa_circ_63407,RMVar_hsa_circ_143889,RMVar_hsa_circ_143890,RMVar_hsa_circ_143888,RMVar_hsa_circ_53594,RMVar_hsa_circ_28048,RMVar_hsa_circ_337764,RMVar_hsa_circ_359965,RMVar_hsa_circ_24449,RMVar_hsa_circ_12168,RMVar_hsa_circ_36191,RMVar_hsa_circ_29756,RMVar_hsa_circ_328870,RMVar_hsa_circ_317570,RMVar_hsa_circ_66975,RMVar_hsa_circ_143901 22245 RMVar_ID_22245 Human_SNP_ID_436537344 A-to-I Human chr10 + 68752688 68752688 68752688 AGGCCAGGAGTTTGAGACCAGCCTAGGCATATAGTGAGACCTCACCTCTACAAAAAGTAGAAGTT AGGCCAGGAGTTTGAGACCAGCCTAGGCATATGGTGAGACCTCACCTCTACAAAAAGTAGAAGTT A G CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1209243550 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5990915,Human_RBP_ID_11401336 RMVar_hsa_circ_14730,RMVar_hsa_circ_333610,RMVar_hsa_circ_356781,RMVar_hsa_circ_367534,RMVar_hsa_circ_307164,RMVar_hsa_circ_306748,RMVar_hsa_circ_37797,RMVar_hsa_circ_7424,RMVar_hsa_circ_124407,RMVar_hsa_circ_1627,RMVar_hsa_circ_143882,RMVar_hsa_circ_143883,RMVar_hsa_circ_344019,RMVar_hsa_circ_107599,RMVar_hsa_circ_115064,RMVar_hsa_circ_63407,RMVar_hsa_circ_143889,RMVar_hsa_circ_143890,RMVar_hsa_circ_143888,RMVar_hsa_circ_53594,RMVar_hsa_circ_28048,RMVar_hsa_circ_337764,RMVar_hsa_circ_359965,RMVar_hsa_circ_24449,RMVar_hsa_circ_12168,RMVar_hsa_circ_36191,RMVar_hsa_circ_29756,RMVar_hsa_circ_328870,RMVar_hsa_circ_317570,RMVar_hsa_circ_66975,RMVar_hsa_circ_143901 22246 RMVar_ID_22246 Human_SNP_ID_436537353 A-to-I Human chr10 + 68752734 68752734 68752734 TCTACAAAAAGTAGAAGTTAGCCACATGTGGTAGTGCACCCGTAGTCCTAGCTATAATACTTAGA TCTACAAAAAGTAGAAGTTAGCCACATGTGGTGGTGCACCCGTAGTCCTAGCTATAATACTTAGA A G CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1050417743 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5990917,Human_RBP_ID_11401338 RMVar_hsa_circ_14730,RMVar_hsa_circ_333610,RMVar_hsa_circ_356781,RMVar_hsa_circ_367534,RMVar_hsa_circ_307164,RMVar_hsa_circ_306748,RMVar_hsa_circ_37797,RMVar_hsa_circ_7424,RMVar_hsa_circ_124407,RMVar_hsa_circ_1627,RMVar_hsa_circ_143882,RMVar_hsa_circ_143883,RMVar_hsa_circ_344019,RMVar_hsa_circ_107599,RMVar_hsa_circ_115064,RMVar_hsa_circ_63407,RMVar_hsa_circ_143889,RMVar_hsa_circ_143890,RMVar_hsa_circ_143888,RMVar_hsa_circ_53594,RMVar_hsa_circ_28048,RMVar_hsa_circ_337764,RMVar_hsa_circ_359965,RMVar_hsa_circ_24449,RMVar_hsa_circ_12168,RMVar_hsa_circ_36191,RMVar_hsa_circ_29756,RMVar_hsa_circ_328870,RMVar_hsa_circ_317570,RMVar_hsa_circ_66975,RMVar_hsa_circ_143901 22247 RMVar_ID_22247 Human_SNP_ID_436538500 A-to-I Human chr10 + 68757434 68757434 68757434 ATTTATTTTTTTCAATTAAAAAGTTCTTTCTGAGATGGAGTCTCGCTCTGTCGCCCAGGCTGGAG ATTTATTTTTTTCAATTAAAAAGTTCTTTCTGCGATGGAGTCTCGCTCTGTCGCCCAGGCTGGAG A C CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1046334367 Functional Loss SNV dbSNP153 33..33 33 - - - 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_52772,RMVar_hsa_circ_308624 22248 RMVar_ID_22248 Human_SNP_ID_436538518 A-to-I Human chr10 + 68757489 68757489 68757489 CAGGCTGGAGTGTAGTGGCGCGATCTCGGCTCACTTCAGCCTCTGCCTCCTGGGTTCAGTAGATT CAGGCTGGAGTGTAGTGGCGCGATCTCGGCTCTCTTCAGCCTCTGCCTCCTGGGTTCAGTAGATT A T CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs993268955 Functional Loss SNV dbSNP153 33..33 33 - - - 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_52772,RMVar_hsa_circ_308624 22249 RMVar_ID_22249 Human_SNP_ID_436538525 A-to-I Human chr10 + 68757532 68757532 68757532 TGCCTCCTGGGTTCAGTAGATTCTCTTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCACCCT TGCCTCCTGGGTTCAGTAGATTCTCTTGCCTCGGCCTCCTGAGTAGCTGGGATTACAGGCACCCT A G CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs149913751 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11401521 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_52772,RMVar_hsa_circ_308624 22250 RMVar_ID_22250 Human_SNP_ID_436538545 A-to-I Human chr10 + 68757605 68757605 68757605 GCCTGGCTAATTTTTCTAGTTTTAGTAGAGACAAGGTTTCAGAATGTTGGCCAGTTTGGTCTCGA GCCTGGCTAATTTTTCTAGTTTTAGTAGAGACGAGGTTTCAGAATGTTGGCCAGTTTGGTCTCGA A G CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE47997;GSE38233;GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 K562 cells&HepG2 cells;cultured B-cells;cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 23474544,24183664,24183664,29129909,31158229 RNA-Seq:(High) rs1277915737 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11401522 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_52772,RMVar_hsa_circ_308624 22251 RMVar_ID_22251 Human_SNP_ID_436538551 A-to-I Human chr10 + 68757625 68757625 68757625 TTTAGTAGAGACAAGGTTTCAGAATGTTGGCCAGTTTGGTCTCGAACTCCTGACATCAGGTGATC TTTAGTAGAGACAAGGTTTCAGAATGTTGGCCGGTTTGGTCTCGAACTCCTGACATCAGGTGATC A G CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1445382248 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11401522 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_52772,RMVar_hsa_circ_308624 22252 RMVar_ID_22252 Human_SNP_ID_436538739 A-to-I Human chr10 + 68758315 68758315 68758315 GGCCTCAAGCGATCTATCCACCCCCGCCTCCCAGAGTGTTAGGATTACAGGCGTGAGCTACTGCG GGCCTCAAGCGATCTATCCACCCCCGCCTCCCCGAGTGTTAGGATTACAGGCGTGAGCTACTGCG A C CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs1276977154 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_224998,Human_RBP_ID_22883692,Human_RBP_ID_24826349 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_52772,RMVar_hsa_circ_308624 22253 RMVar_ID_22253 Human_SNP_ID_436539012 A-to-I Human chr10 + 68758802 68758802 68758802 TCAAGAGATTCTCGTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCCTGTGCCACCATGCCTG TCAAGAGATTCTCGTGCCTCAGCCTCCCGAGTGGCTGGGACTACAGGCCTGTGCCACCATGCCTG A G CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE38233;GSE100210;GSE99789 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 24183664,29129909,29796672 RNA-Seq:(High) rs981133103 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24826356 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_52772,RMVar_hsa_circ_308624 22254 RMVar_ID_22254 Human_SNP_ID_436539019 A-to-I Human chr10 + 68758814 68758814 68758814 CGTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCCTGTGCCACCATGCCTGACTAATTTTTGT CGTGCCTCAGCCTCCCGAGTAGCTGGGACTACGGGCCTGTGCCACCATGCCTGACTAATTTTTGT A G CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs957512019 Functional Loss SNV dbSNP153 33..33 33 - - - 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_52772,RMVar_hsa_circ_308624 22255 RMVar_ID_22255 Human_SNP_ID_436539028 A-to-I Human chr10 + 68758858 68758858 68758858 CCATGCCTGACTAATTTTTGTATGTTTAGTAGAGATGGGGTTTCACCATATTGGCCAGGCTGGTC CCATGCCTGACTAATTTTTGTATGTTTAGTAGGGATGGGGTTTCACCATATTGGCCAGGCTGGTC A G CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1694335 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2015,GWAS_ID_2016,GWAS_ID_2017,GWAS_ID_2018,GWAS_ID_2019,GWAS_ID_2020,GWAS_ID_2021,GWAS_ID_2022,GWAS_ID_2023,GWAS_ID_2024,GWAS_ID_2025,GWAS_ID_2026,GWAS_ID_2027,GWAS_ID_2028,GWAS_ID_2029,GWAS_ID_2030,GWAS_ID_2031,GWAS_ID_2032,GWAS_ID_2033,GWAS_ID_2034,GWAS_ID_2035,GWAS_ID_2036,GWAS_ID_2037,GWAS_ID_2038,GWAS_ID_2039,GWAS_ID_2040,GWAS_ID_2041,GWAS_ID_2042,GWAS_ID_2043 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_52772,RMVar_hsa_circ_308624 22256 RMVar_ID_22256 Human_SNP_ID_436539029 A-to-I Human chr10 + 68758858 68758858 68758858 CCATGCCTGACTAATTTTTGTATGTTTAGTAGAGATGGGGTTTCACCATATTGGCCAGGCTGGTC CCATGCCTGACTAATTTTTGTATGTTTAGTAGTGATGGGGTTTCACCATATTGGCCAGGCTGGTC A T CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1694335 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2015,GWAS_ID_2016,GWAS_ID_2017,GWAS_ID_2018,GWAS_ID_2019,GWAS_ID_2020,GWAS_ID_2021,GWAS_ID_2022,GWAS_ID_2023,GWAS_ID_2024,GWAS_ID_2025,GWAS_ID_2026,GWAS_ID_2027,GWAS_ID_2028,GWAS_ID_2029,GWAS_ID_2030,GWAS_ID_2031,GWAS_ID_2032,GWAS_ID_2033,GWAS_ID_2034,GWAS_ID_2035,GWAS_ID_2036,GWAS_ID_2037,GWAS_ID_2038,GWAS_ID_2039,GWAS_ID_2040,GWAS_ID_2041,GWAS_ID_2042,GWAS_ID_2043 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_52772,RMVar_hsa_circ_308624 22257 RMVar_ID_22257 Human_SNP_ID_436539049 A-to-I Human chr10 + 68758932 68758932 68758932 GACCTCAATTGATCCACCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGATGTGATCCTCCTCC GACCTCAATTGATCCACCCACCTCAGCCTCCCCAAGTGCTGGGATTACAGATGTGATCCTCCTCC A C CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1306750035 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23464574 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_52772,RMVar_hsa_circ_308624 22258 RMVar_ID_22258 Human_SNP_ID_436539092 A-to-I Human chr10 + 68759098 68759098 68759098 GTTACGATCACTTCAACCCAAGGATACTGAATAGAAAAAACAACAACCAACAACCATAAAGTAAT GTTACGATCACTTCAACCCAAGGATACTGAATGGAAAAAACAACAACCAACAACCATAAAGTAAT A G CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1248400783 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1769422,Human_RBP_ID_3355103,Human_RBP_ID_4124130,Human_RBP_ID_11401579,Human_RBP_ID_17559303,Human_RBP_ID_18596687 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_52772,RMVar_hsa_circ_308624 22259 RMVar_ID_22259 Human_SNP_ID_436539117 A-to-I Human chr10 + 68759230 68759230 68759230 CAGTCTAGGAGTTTGAGATCAGCTTCTGCAACATAGTGAGGCCCTGTCTCTACAAAAAGTTTAAA CAGTCTAGGAGTTTGAGATCAGCTTCTGCAACGTAGTGAGGCCCTGTCTCTACAAAAAGTTTAAA A G CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1183146757 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22883697,Human_RBP_ID_23464579 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_52772,RMVar_hsa_circ_308624 22260 RMVar_ID_22260 Human_SNP_ID_436539174 A-to-I Human chr10 + 68759503 68759502 68759503 TAATCCTAGCACTTTTGGAGGCCCAGATGGGCAGATTGCTATAGCCCAGTAGTTCAAGATCAGCC TAATCCTAGCACTTTTGGAGGCCCAGATGGGAGGATTGCTATAGCCCAGTAGTTCAAGATCAGCC CA AG CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs34640023 Functional Loss MNV dbSNP153 32..33 33 - - - Human_RBP_ID_224999 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_52772,RMVar_hsa_circ_308624 22261 RMVar_ID_22261 Human_SNP_ID_436539192 A-to-I Human chr10 + 68759577 68759577 68759577 TACTGAGACTCTCTACCAAAAAAAAAAAAATTAGCTGAGCATGGTGATGCATGCCTATAGTCCTA TACTGAGACTCTCTACCAAAAAAAAAAAAATTGGCTGAGCATGGTGATGCATGCCTATAGTCCTA A G CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE38233;GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,32596459 RNA-Seq:(High) rs998026520 Functional Loss SNV dbSNP153 33..33 33 - - - 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_52772,RMVar_hsa_circ_308624 22262 RMVar_ID_22262 Human_SNP_ID_436539193 A-to-I Human chr10 + 68759577 68759577 68759577 TACTGAGACTCTCTACCAAAAAAAAAAAAATTAGCTGAGCATGGTGATGCATGCCTATAGTCCTA TACTGAGACTCTCTACCAAAAAAAAAAAAATTTGCTGAGCATGGTGATGCATGCCTATAGTCCTA A T CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE38233;GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,32596459 RNA-Seq:(High) rs998026520 Functional Loss SNV dbSNP153 33..33 33 - - - 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_52772,RMVar_hsa_circ_308624 22263 RMVar_ID_22263 Human_SNP_ID_436539199 A-to-I Human chr10 + 68759601 68759601 68759601 AAAAAATTAGCTGAGCATGGTGATGCATGCCTATAGTCCTAGCTACTCAGGAGCCTGAGGTGGGA AAAAAATTAGCTGAGCATGGTGATGCATGCCTGTAGTCCTAGCTACTCAGGAGCCTGAGGTGGGA A G CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,31158229,31158229,32596459 RNA-Seq:(High) rs1339463618 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17559305,Human_RBP_ID_22567562 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_52772,RMVar_hsa_circ_308624 22264 RMVar_ID_22264 Human_SNP_ID_436539298 A-to-I Human chr10 + 68759951 68759951 68759951 CAAACTCCTAGGCTCAAGTGGTCCTCTGACCTAAGCCTCTCAAGTAGCTTGGGCTAAAGACATGT CAAACTCCTAGGCTCAAGTGGTCCTCTGACCTGAGCCTCTCAAGTAGCTTGGGCTAAAGACATGT A G CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1362350834 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11401620 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_52772,RMVar_hsa_circ_308624 22265 RMVar_ID_22265 Human_SNP_ID_436539301 A-to-I Human chr10 + 68759980 68759979 68759981 CCTAAGCCTCTCAAGTAGCTTGGGCTAAAGACATGTTCCACCATGCCTGGCTAATTTTTTTTTCT CCTAAGCCTCTCAAGTAGCTTGGGCTAAAGAC__GTTCCACCATGCCTGGCTAATTTTTTTTTCT CAT C CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1198519291 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_11401632 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_52772,RMVar_hsa_circ_308624 22266 RMVar_ID_22266 Human_SNP_ID_436539302 A-to-I Human chr10 + 68759980 68759980 68759980 CCTAAGCCTCTCAAGTAGCTTGGGCTAAAGACATGTTCCACCATGCCTGGCTAATTTTTTTTTCT CCTAAGCCTCTCAAGTAGCTTGGGCTAAAGACGTGTTCCACCATGCCTGGCTAATTTTTTTTTCT A G CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1431366521 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11401632 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_52772,RMVar_hsa_circ_308624 22267 RMVar_ID_22267 Human_SNP_ID_436539388 A-to-I Human chr10 + 68760265 68760265 68760265 AAACTCCTGGGCTCAAGCAGTCTTCCCATCTCAGCCTCCCAAGTGGTTAGGACTACAGGCATTCA AAACTCCTGGGCTCAAGCAGTCTTCCCATCTCGGCCTCCCAAGTGGTTAGGACTACAGGCATTCA A G CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1488791398 Functional Loss SNV dbSNP153 33..33 33 - - - 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_52772,RMVar_hsa_circ_308624 22268 RMVar_ID_22268 Human_SNP_ID_436539510 A-to-I Human chr10 + 68760753 68760753 68760753 GGATGTGATTGTGCGCATCTGTAATCCCAGCTACTTGGGGGGCTGAGACAGGAGAATTGCTTGAA GGATGTGATTGTGCGCATCTGTAATCCCAGCTCCTTGGGGGGCTGAGACAGGAGAATTGCTTGAA A C CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1364036953 Functional Loss SNV dbSNP153 33..33 33 - - - 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_52772,RMVar_hsa_circ_308624 22269 RMVar_ID_22269 Human_SNP_ID_436539523 A-to-I Human chr10 + 68760770 68760770 68760770 TCTGTAATCCCAGCTACTTGGGGGGCTGAGACAGGAGAATTGCTTGAACCTGGGAGGCAGAGCTT TCTGTAATCCCAGCTACTTGGGGGGCTGAGACGGGAGAATTGCTTGAACCTGGGAGGCAGAGCTT A G CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs922403611 Functional Loss SNV dbSNP153 33..33 33 - - - 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_52772,RMVar_hsa_circ_308624 22270 RMVar_ID_22270 Human_SNP_ID_436539540 A-to-I Human chr10 + 68760819 68760818 68760819 CTGGGAGGCAGAGCTTGTGGTAAGCCGAGATCACGCCACTGCACTCCAGCCTGGGCGACAGAGTT CTGGGAGGCAGAGCTTGTGGTAAGCCGAGATC_CGCCACTGCACTCCAGCCTGGGCGACAGAGTT CA C CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1469069716 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_2228163,Human_RBP_ID_11401680,Human_RBP_ID_24826402 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_52772,RMVar_hsa_circ_308624 22271 RMVar_ID_22271 Human_SNP_ID_436541746 A-to-I Human chr10 + 68769104 68769104 68769104 TGAAGCAATTCTCCTGCCTCGACGTCCCGAGTAGCCCTGGGATTACAGGCGTGTGCCTACACACC TGAAGCAATTCTCCTGCCTCGACGTCCCGAGTGGCCCTGGGATTACAGGCGTGTGCCTACACACC A G CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs527784930 Functional Loss SNV dbSNP153 33..33 33 - - - 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_143910,RMVar_hsa_circ_27926 22272 RMVar_ID_22272 Human_SNP_ID_436541747 A-to-I Human chr10 + 68769104 68769104 68769104 TGAAGCAATTCTCCTGCCTCGACGTCCCGAGTAGCCCTGGGATTACAGGCGTGTGCCTACACACC TGAAGCAATTCTCCTGCCTCGACGTCCCGAGTTGCCCTGGGATTACAGGCGTGTGCCTACACACC A T CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs527784930 Functional Loss SNV dbSNP153 33..33 33 - - - 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_143910,RMVar_hsa_circ_27926 22273 RMVar_ID_22273 Human_SNP_ID_436541756 A-to-I Human chr10 + 68769134 68769134 68769134 GTAGCCCTGGGATTACAGGCGTGTGCCTACACACCCAGCTAATTTTTGTATTTTTAGTAAAGACA GTAGCCCTGGGATTACAGGCGTGTGCCTACACCCCCAGCTAATTTTTGTATTTTTAGTAAAGACA A C CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1432125273 Functional Loss SNV dbSNP153 33..33 33 - - - 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_143910,RMVar_hsa_circ_27926 22274 RMVar_ID_22274 Human_SNP_ID_436541846 A-to-I Human chr10 + 68769419 68769419 68769419 GAGGCAGGCGGATCGCCTGAGTTCAGGAGTTCAAGACCAGCCTGACCAACATGGAGAAACCCCAT GAGGCAGGCGGATCGCCTGAGTTCAGGAGTTCGAGACCAGCCTGACCAACATGGAGAAACCCCAT A G CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs193269841 Functional Loss SNV dbSNP153 33..33 33 - - - 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_143910,RMVar_hsa_circ_27926 22275 RMVar_ID_22275 Human_SNP_ID_436542090 A-to-I Human chr10 + 68770160 68770160 68770160 ATGTCACCTTATCAGAGAGGCCTTGTCTTACTATTCTCTCTTGTTATACTCTAGGTGTTTATCCT ATGTCACCTTATCAGAGAGGCCTTGTCTTACTCTTCTCTCTTGTTATACTCTAGGTGTTTATCCT A C CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs9415936 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5991069,Human_RBP_ID_19536327 GWAS_ID_2044,GWAS_ID_2045,GWAS_ID_2046,GWAS_ID_2047,GWAS_ID_2048,GWAS_ID_2049,GWAS_ID_2050,GWAS_ID_2051,GWAS_ID_2052,GWAS_ID_2053,GWAS_ID_2054,GWAS_ID_2055,GWAS_ID_2056,GWAS_ID_2057,GWAS_ID_2058,GWAS_ID_2059,GWAS_ID_2060,GWAS_ID_2061,GWAS_ID_2062,GWAS_ID_2063,GWAS_ID_2064,GWAS_ID_2065,GWAS_ID_2066,GWAS_ID_2067,GWAS_ID_2068,GWAS_ID_2069,GWAS_ID_2070,GWAS_ID_2071,GWAS_ID_2072 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_143910,RMVar_hsa_circ_27926 22276 RMVar_ID_22276 Human_SNP_ID_436542091 A-to-I Human chr10 + 68770160 68770160 68770160 ATGTCACCTTATCAGAGAGGCCTTGTCTTACTATTCTCTCTTGTTATACTCTAGGTGTTTATCCT ATGTCACCTTATCAGAGAGGCCTTGTCTTACTGTTCTCTCTTGTTATACTCTAGGTGTTTATCCT A G CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs9415936 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5991069,Human_RBP_ID_19536327 GWAS_ID_2044,GWAS_ID_2045,GWAS_ID_2046,GWAS_ID_2047,GWAS_ID_2048,GWAS_ID_2049,GWAS_ID_2050,GWAS_ID_2051,GWAS_ID_2052,GWAS_ID_2053,GWAS_ID_2054,GWAS_ID_2055,GWAS_ID_2056,GWAS_ID_2057,GWAS_ID_2058,GWAS_ID_2059,GWAS_ID_2060,GWAS_ID_2061,GWAS_ID_2062,GWAS_ID_2063,GWAS_ID_2064,GWAS_ID_2065,GWAS_ID_2066,GWAS_ID_2067,GWAS_ID_2068,GWAS_ID_2069,GWAS_ID_2070,GWAS_ID_2071,GWAS_ID_2072 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_143910,RMVar_hsa_circ_27926 22277 RMVar_ID_22277 Human_SNP_ID_436542092 A-to-I Human chr10 + 68770160 68770160 68770160 ATGTCACCTTATCAGAGAGGCCTTGTCTTACTATTCTCTCTTGTTATACTCTAGGTGTTTATCCT ATGTCACCTTATCAGAGAGGCCTTGTCTTACTTTTCTCTCTTGTTATACTCTAGGTGTTTATCCT A T CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs9415936 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5991069,Human_RBP_ID_19536327 GWAS_ID_2044,GWAS_ID_2045,GWAS_ID_2046,GWAS_ID_2047,GWAS_ID_2048,GWAS_ID_2049,GWAS_ID_2050,GWAS_ID_2051,GWAS_ID_2052,GWAS_ID_2053,GWAS_ID_2054,GWAS_ID_2055,GWAS_ID_2056,GWAS_ID_2057,GWAS_ID_2058,GWAS_ID_2059,GWAS_ID_2060,GWAS_ID_2061,GWAS_ID_2062,GWAS_ID_2063,GWAS_ID_2064,GWAS_ID_2065,GWAS_ID_2066,GWAS_ID_2067,GWAS_ID_2068,GWAS_ID_2069,GWAS_ID_2070,GWAS_ID_2071,GWAS_ID_2072 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_143910,RMVar_hsa_circ_27926 22278 RMVar_ID_22278 Human_SNP_ID_436542605 A-to-I Human chr10 + 68772020 68772020 68772020 AGTCTCCCAAGTAGCTGAGACTACAGGTGCACACCACCTTGCCCAGCTAATTTTTTTGTTTGTTT AGTCTCCCAAGTAGCTGAGACTACAGGTGCACTCCACCTTGCCCAGCTAATTTTTTTGTTTGTTT A T CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1417832731 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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 22279 RMVar_ID_22279 Human_SNP_ID_436542694 A-to-I Human chr10 + 68772352 68772352 68772352 AAAAATTAGGAAAATTAGCTGGACATGGTGGCATGTGCCTGTGGTCCCAGCTACTTGGGAGGGTG AAAAATTAGGAAAATTAGCTGGACATGGTGGCGTGTGCCTGTGGTCCCAGCTACTTGGGAGGGTG A G CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1347524343 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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 22280 RMVar_ID_22280 Human_SNP_ID_436543004 A-to-I Human chr10 + 68773452 68773452 68773452 TGGGAGGCCAAGGCAGGTGATCATTTGAGGTCAAGAGTTCCAAGTCCAGCCTTGCCAACATGGTG TGGGAGGCCAAGGCAGGTGATCATTTGAGGTCGAGAGTTCCAAGTCCAGCCTTGCCAACATGGTG A G CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1694488 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11401918,Human_RBP_ID_24826589 GWAS_ID_2073,GWAS_ID_2074,GWAS_ID_2075,GWAS_ID_2076,GWAS_ID_2077,GWAS_ID_2078,GWAS_ID_2079,GWAS_ID_2080,GWAS_ID_2081,GWAS_ID_2082,GWAS_ID_2083,GWAS_ID_2084,GWAS_ID_2085,GWAS_ID_2086,GWAS_ID_2087,GWAS_ID_2088,GWAS_ID_2089,GWAS_ID_2090,GWAS_ID_2091,GWAS_ID_2092,GWAS_ID_2093,GWAS_ID_2094,GWAS_ID_2095,GWAS_ID_2096,GWAS_ID_2097,GWAS_ID_2098,GWAS_ID_2099,GWAS_ID_2100,GWAS_ID_2101 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 22281 RMVar_ID_22281 Human_SNP_ID_436543005 A-to-I Human chr10 + 68773452 68773452 68773452 TGGGAGGCCAAGGCAGGTGATCATTTGAGGTCAAGAGTTCCAAGTCCAGCCTTGCCAACATGGTG TGGGAGGCCAAGGCAGGTGATCATTTGAGGTCTAGAGTTCCAAGTCCAGCCTTGCCAACATGGTG A T CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1694488 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11401918,Human_RBP_ID_24826589 GWAS_ID_2073,GWAS_ID_2074,GWAS_ID_2075,GWAS_ID_2076,GWAS_ID_2077,GWAS_ID_2078,GWAS_ID_2079,GWAS_ID_2080,GWAS_ID_2081,GWAS_ID_2082,GWAS_ID_2083,GWAS_ID_2084,GWAS_ID_2085,GWAS_ID_2086,GWAS_ID_2087,GWAS_ID_2088,GWAS_ID_2089,GWAS_ID_2090,GWAS_ID_2091,GWAS_ID_2092,GWAS_ID_2093,GWAS_ID_2094,GWAS_ID_2095,GWAS_ID_2096,GWAS_ID_2097,GWAS_ID_2098,GWAS_ID_2099,GWAS_ID_2100,GWAS_ID_2101 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 22282 RMVar_ID_22282 Human_SNP_ID_436543027 A-to-I Human chr10 + 68773541 68773541 68773541 AAAAATTAGCCAGGCGGTAGTGGCGCGTGCCTATAATCCCAGGTATACTCTGGAGGCTGAGGCAG AAAAATTAGCCAGGCGGTAGTGGCGCGTGCCTGTAATCCCAGGTATACTCTGGAGGCTGAGGCAG A G CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1024764030 Functional Loss SNV dbSNP153 33..33 33 - - - 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 22283 RMVar_ID_22283 Human_SNP_ID_436543036 A-to-I Human chr10 + 68773581 68773581 68773581 AGGTATACTCTGGAGGCTGAGGCAGGAGAATCACTTGAGCATGGGAGGCGGAGGTTGTGGTGAGC AGGTATACTCTGGAGGCTGAGGCAGGAGAATCGCTTGAGCATGGGAGGCGGAGGTTGTGGTGAGC A G CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs975192240 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11401920 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 22284 RMVar_ID_22284 Human_SNP_ID_436543106 A-to-I Human chr10 + 68773852 68773852 68773852 CTCTCACCTCAGTCCCTGGAGTAACTGGGACTACAGGTGCTTGCCACCATTCCTGGCTAATTTTT CTCTCACCTCAGTCCCTGGAGTAACTGGGACTGCAGGTGCTTGCCACCATTCCTGGCTAATTTTT A G CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1333428133 Functional Loss SNV dbSNP153 33..33 33 - - - 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 22285 RMVar_ID_22285 Human_SNP_ID_436543302 A-to-I Human chr10 + 68774542 68774542 68774542 AATACCAGCTTCTGGGGAGGCTGAGGCGGGAGAATGGCTTGAACTCGGGAGGCAGAGGTTGCAGC AATACCAGCTTCTGGGGAGGCTGAGGCGGGAGGATGGCTTGAACTCGGGAGGCAGAGGTTGCAGC A G CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1316061270 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17558812,Human_RBP_ID_24826611 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 22286 RMVar_ID_22286 Human_SNP_ID_436543303 A-to-I Human chr10 + 68774551 68774551 68774551 TTCTGGGGAGGCTGAGGCGGGAGAATGGCTTGAACTCGGGAGGCAGAGGTTGCAGCGAGCCCAGA TTCTGGGGAGGCTGAGGCGGGAGAATGGCTTGGACTCGGGAGGCAGAGGTTGCAGCGAGCCCAGA A G CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs957695868 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1159474,Human_RBP_ID_17558812 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 22287 RMVar_ID_22287 Human_SNP_ID_436543740 A-to-I Human chr10 + 68775880 68775880 68775880 CACCACACCTTGCTAATTTTTGTATTTATGGTAGAGACGGAGTTTTACCATGTTGGCCAGACTGG CACCACACCTTGCTAATTTTTGTATTTATGGTGGAGACGGAGTTTTACCATGTTGGCCAGACTGG A G CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs889998591 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5991110,Human_RBP_ID_11401966,Human_RBP_ID_22883726,Human_RBP_ID_23152569 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 22288 RMVar_ID_22288 Human_SNP_ID_436543759 A-to-I Human chr10 + 68775956 68775956 68775956 TGACCAGGTGGTCCTCCCGTCTTGGCCTCCCAAAGTGCTGGAGTTATAGACATGGGCCACTGCGC TGACCAGGTGGTCCTCCCGTCTTGGCCTCCCATAGTGCTGGAGTTATAGACATGGGCCACTGCGC A T CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs901287030 Functional Loss SNV dbSNP153 33..33 33 - - - 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 22289 RMVar_ID_22289 Human_SNP_ID_436543871 A-to-I Human chr10 + 68776373 68776373 68776373 ATCACCTGAGGTCAGGAGTTCGAGACCAGCCTAGCCAACATATTGAAAACCCCACCTCTAGTAAA ATCACCTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATATTGAAAACCCCACCTCTAGTAAA A G CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1234745986 Functional Loss SNV dbSNP153 33..33 33 - - - 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 22290 RMVar_ID_22290 Human_SNP_ID_436543872 A-to-I Human chr10 + 68776382 68776382 68776382 GGTCAGGAGTTCGAGACCAGCCTAGCCAACATATTGAAAACCCCACCTCTAGTAAAAATACAAAA GGTCAGGAGTTCGAGACCAGCCTAGCCAACATGTTGAAAACCCCACCTCTAGTAAAAATACAAAA A G CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037305400 Functional Loss SNV dbSNP153 33..33 33 - - - 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 22291 RMVar_ID_22291 Human_SNP_ID_436543911 A-to-I Human chr10 + 68776521 68776521 68776521 CCAGGAGGCGGAGGTTGCGGTGAACCGAGATCACGCCATTGCACTCCAGCCTGGGCAGCAATAGC CCAGGAGGCGGAGGTTGCGGTGAACCGAGATCGCGCCATTGCACTCCAGCCTGGGCAGCAATAGC A G CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1199563624 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11401985,Human_RBP_ID_22470861 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 22292 RMVar_ID_22292 Human_SNP_ID_436543978 A-to-I Human chr10 + 68776746 68776746 68776746 AGCTGTTTAATTTTTTGTAGAGATGGGGTCTCAGTATGTTGCCCAGGCTGGTCTTGACCTCCTTG AGCTGTTTAATTTTTTGTAGAGATGGGGTCTCGGTATGTTGCCCAGGCTGGTCTTGACCTCCTTG A G CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1469678538 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11401988,Human_RBP_ID_17559011 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 22293 RMVar_ID_22293 Human_SNP_ID_436544147 A-to-I Human chr10 + 68777425 68777425 68777425 TGTTCAGGCTGGGCATGGTGGCTCACGCCTGTAATCTCAGCACTTTGTGGGAGGCCGAGGCGGGT TGTTCAGGCTGGGCATGGTGGCTCACGCCTGTCATCTCAGCACTTTGTGGGAGGCCGAGGCGGGT A C CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs149056302 Functional Loss SNV dbSNP153 33..33 33 - - - 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 22294 RMVar_ID_22294 Human_SNP_ID_436544182 A-to-I Human chr10 + 68777577 68777576 68777578 ATGGTGGCGCGCACCTGTAATCCCAGCTGCTCAAGAGGCTGAGGCGTGAGAATCACTTGAACACA ATGGTGGCGCGCACCTGTAATCCCAGCTGCTC__GAGGCTGAGGCGTGAGAATCACTTGAACACA CAA C CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1209257403 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_11402003 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 22295 RMVar_ID_22295 Human_SNP_ID_436544189 A-to-I Human chr10 + 68777599 68777599 68777599 CCAGCTGCTCAAGAGGCTGAGGCGTGAGAATCACTTGAACACAGAAGGTGGAGGTTGCAGTGAGC CCAGCTGCTCAAGAGGCTGAGGCGTGAGAATCGCTTGAACACAGAAGGTGGAGGTTGCAGTGAGC A G CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1408299900 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11402004 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 22296 RMVar_ID_22296 Human_SNP_ID_436544342 A-to-I Human chr10 + 68778179 68778179 68778179 CAGAGGTTGCAGTGAGCCGAGATTGTGCCACTACGTTCCAGCCTGGGTGACAAAGCAAGACTCCA CAGAGGTTGCAGTGAGCCGAGATTGTGCCACTGCGTTCCAGCCTGGGTGACAAAGCAAGACTCCA A G CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1323025195 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24860101 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 22297 RMVar_ID_22297 Human_SNP_ID_436544523 A-to-I Human chr10 + 68778920 68778920 68778920 GTCACCAGGCTGGAGTGCACTGGTGCGATCTCAGCTCACTCCAACCTCCGCCTCCCGGATTCAAG GTCACCAGGCTGGAGTGCACTGGTGCGATCTCCGCTCACTCCAACCTCCGCCTCCCGGATTCAAG A C CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1009426909 Functional Loss SNV dbSNP153 33..33 33 - - - 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 22298 RMVar_ID_22298 Human_SNP_ID_436545059 A-to-I Human chr10 + 68781111 68781111 68781111 CAAAATAGCCAGGTGTGGTGGTGTACGCTTGTAATACCAGCTACTCGGGAGGCTGGGGGCATGAG CAAAATAGCCAGGTGTGGTGGTGTACGCTTGTTATACCAGCTACTCGGGAGGCTGGGGGCATGAG A T CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1256512218 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5991153,Human_RBP_ID_11402092,Human_RBP_ID_24826716 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 22299 RMVar_ID_22299 Human_SNP_ID_436547058 A-to-I Human chr10 + 68788504 68788504 68788504 TTTTTAAAATTTTTTATTATTTATTTGTTTTTAAGACAGGGTCTCACTCCGTTACCCAAGTGGAG TTTTTAAAATTTTTTATTATTTATTTGTTTTTGAGACAGGGTCTCACTCCGTTACCCAAGTGGAG A G CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1049638805 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115064,RMVar_hsa_circ_143888,RMVar_hsa_circ_268652,RMVar_hsa_circ_143906,RMVar_hsa_circ_69537,RMVar_hsa_circ_143913,RMVar_hsa_circ_272077,RMVar_hsa_circ_143914,RMVar_hsa_circ_143917,RMVar_hsa_circ_56157,RMVar_hsa_circ_308425,RMVar_hsa_circ_143918,RMVar_hsa_circ_310182 22300 RMVar_ID_22300 Human_SNP_ID_436547218 A-to-I Human chr10 + 68789161 68789161 68789161 TCGATCTCCTGACCTCGTGATCCGCCCACCTCAGCCTCCCAAAGTGCTGGGTTTACAGGCATGAG TCGATCTCCTGACCTCGTGATCCGCCCACCTCGGCCTCCCAAAGTGCTGGGTTTACAGGCATGAG A G CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs58630866 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115064,RMVar_hsa_circ_143888,RMVar_hsa_circ_268652,RMVar_hsa_circ_143906,RMVar_hsa_circ_69537,RMVar_hsa_circ_143913,RMVar_hsa_circ_272077,RMVar_hsa_circ_143914,RMVar_hsa_circ_143917,RMVar_hsa_circ_56157,RMVar_hsa_circ_308425,RMVar_hsa_circ_143918,RMVar_hsa_circ_310182 22301 RMVar_ID_22301 Human_SNP_ID_436547307 A-to-I Human chr10 + 68789511 68789510 68789512 AGATCGTGCCACTTCGCTCAAGCTGGCGCAACAGAGTGAGACTCAGTCTCAAAAGTAAATACATA AGATCGTGCCACTTCGCTCAAGCTGGCGCAAC__AGTGAGACTCAGTCTCAAAAGTAAATACATA CAG C CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs780917142 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_115064,RMVar_hsa_circ_143888,RMVar_hsa_circ_268652,RMVar_hsa_circ_143906,RMVar_hsa_circ_69537,RMVar_hsa_circ_143913,RMVar_hsa_circ_272077,RMVar_hsa_circ_143914,RMVar_hsa_circ_143917,RMVar_hsa_circ_56157,RMVar_hsa_circ_308425,RMVar_hsa_circ_143918,RMVar_hsa_circ_310182 22302 RMVar_ID_22302 Human_SNP_ID_436548130 A-to-I Human chr10 + 68792923 68792923 68792923 CCCCTGCCTTAGCCTCTCAAGTAGCTGGGATTACAGACGTCTGCCACCATGTTCAGCTAATTTTG CCCCTGCCTTAGCCTCTCAAGTAGCTGGGATTGCAGACGTCTGCCACCATGTTCAGCTAATTTTG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs896389932 Functional Loss SNV dbSNP153 33..33 33 - - - 22303 RMVar_ID_22303 Human_SNP_ID_436580719 A-to-I Human chr10 + 68920185 68920185 68920185 ATTTTATCAGTTTTGTTTGTTTGTCTTGAGACAGGGTCTCCCTCTTATGCCCAGGCTGGAGTGCA ATTTTATCAGTTTTGTTTGTTTGTCTTGAGACGGGGTCTCCCTCTTATGCCCAGGCTGGAGTGCA A G DDX50 Ensembl:ENSG00000107625 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1341590989 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1665,RMVar_hsa_circ_47167,RMVar_hsa_circ_16645,RMVar_hsa_circ_42255,RMVar_hsa_circ_44208,RMVar_hsa_circ_97195,RMVar_hsa_circ_125543,RMVar_hsa_circ_26000,RMVar_hsa_circ_63580,RMVar_hsa_circ_143926,RMVar_hsa_circ_143925,RMVar_hsa_circ_349560,RMVar_hsa_circ_338711,RMVar_hsa_circ_5577 22304 RMVar_ID_22304 Human_SNP_ID_436582822 A-to-I Human chr10 + 68928437 68928437 68928437 TTACATCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGAGGATCACTTGAGCTCAGGAGTTTA TTACATCTGTAATCCCAGCACTTTGGGAGGCCCAGGCAGGAGGATCACTTGAGCTCAGGAGTTTA A C DDX50 Ensembl:ENSG00000107625 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1015166845 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1665,RMVar_hsa_circ_47167,RMVar_hsa_circ_16645,RMVar_hsa_circ_42255,RMVar_hsa_circ_44208,RMVar_hsa_circ_97195,RMVar_hsa_circ_125543,RMVar_hsa_circ_26000,RMVar_hsa_circ_63580,RMVar_hsa_circ_143926,RMVar_hsa_circ_143925,RMVar_hsa_circ_349560,RMVar_hsa_circ_338711,RMVar_hsa_circ_5577 22305 RMVar_ID_22305 Human_SNP_ID_436594628 A-to-I Human chr10 + 68975926 68975926 68975926 AAAAAAATAGCCAGGCGTGGTTGCGCACGCCTATAATCCCAGGTACTTGGGAGGCTGAGGCAGGA AAAAAAATAGCCAGGCGTGGTTGCGCACGCCTGTAATCCCAGGTACTTGGGAGGCTGAGGCAGGA A G DDX21 Ensembl:ENSG00000165732 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1462695527 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114654,RMVar_hsa_circ_108868,RMVar_hsa_circ_143937,RMVar_hsa_circ_143941,RMVar_hsa_circ_36404,RMVar_hsa_circ_125854,RMVar_hsa_circ_143945,RMVar_hsa_circ_125290,RMVar_hsa_circ_117373,RMVar_hsa_circ_143955,RMVar_hsa_circ_143956,RMVar_hsa_circ_17128,RMVar_hsa_circ_52600,RMVar_hsa_circ_143959,RMVar_hsa_circ_335961,RMVar_hsa_circ_346794,RMVar_hsa_circ_113176,RMVar_hsa_circ_143962,RMVar_hsa_circ_143963,RMVar_hsa_circ_321347,RMVar_hsa_circ_143965,RMVar_hsa_circ_299209,RMVar_hsa_circ_143967,RMVar_hsa_circ_115262,RMVar_hsa_circ_143968 22306 RMVar_ID_22306 Human_SNP_ID_436594687 A-to-I Human chr10 + 68976144 68976144 68976144 AGCTACTCTGGAGGCTGAGATGGGAGGATTGCATGAGCCCAGGAGGTTGAGGCTGCAGTGAGCTG AGCTACTCTGGAGGCTGAGATGGGAGGATTGCGTGAGCCCAGGAGGTTGAGGCTGCAGTGAGCTG A G DDX21 Ensembl:ENSG00000165732 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs866958115 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114654,RMVar_hsa_circ_108868,RMVar_hsa_circ_143937,RMVar_hsa_circ_143941,RMVar_hsa_circ_36404,RMVar_hsa_circ_125854,RMVar_hsa_circ_143945,RMVar_hsa_circ_125290,RMVar_hsa_circ_117373,RMVar_hsa_circ_143955,RMVar_hsa_circ_143956,RMVar_hsa_circ_17128,RMVar_hsa_circ_52600,RMVar_hsa_circ_143959,RMVar_hsa_circ_335961,RMVar_hsa_circ_346794,RMVar_hsa_circ_113176,RMVar_hsa_circ_143962,RMVar_hsa_circ_143963,RMVar_hsa_circ_321347,RMVar_hsa_circ_143965,RMVar_hsa_circ_299209,RMVar_hsa_circ_143967,RMVar_hsa_circ_115262,RMVar_hsa_circ_143968 22307 RMVar_ID_22307 Human_SNP_ID_436603271 A-to-I Human chr10 + 69012750 69012750 69012750 CCTGTCTCTACCAAAAATACAAAAAATTAGCCAGGCATGGTGGTGTGCACCTATAGTCCCAGCTA CCTGTCTCTACCAAAAATACAAAAAATTAGCCCGGCATGGTGGTGTGCACCTATAGTCCCAGCTA A C KIFBP Ensembl:ENSG00000198954 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs878872140 Functional Loss SNV dbSNP153 33..33 33 - - - 22308 RMVar_ID_22308 Human_SNP_ID_436624212 A-to-I Human chr10 + 69095197 69095197 69095197 GGATATGATTGTGGGCACCTGTCATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAA GGATATGATTGTGGGCACCTGTCATCCCAGCTGCTCGGGAGGCTGAGGCAGGAGAATCGCTTGAA A G SRGN Ensembl:ENSG00000122862 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs182109538 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_143976,RMVar_hsa_circ_378499 22309 RMVar_ID_22309 Human_SNP_ID_436625317 A-to-I Human chr10 + 69099426 69099426 69099426 CTCCTCAAGTGATCTTCCTGCCTCAGCCTCCCAAGTAGCGGGACCACAGGCACACAGCACCATGC CTCCTCAAGTGATCTTCCTGCCTCAGCCTCCCCAGTAGCGGGACCACAGGCACACAGCACCATGC A C SRGN Ensembl:ENSG00000122862 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs900254342 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122072,RMVar_hsa_circ_143977 22310 RMVar_ID_22310 Human_SNP_ID_436625399 A-to-I Human chr10 + 69099842 69099841 69099842 TAAAATGTTAGGCTGCAGTGGCTCATGCCTGTAATCCCCCCAGTTTGGGAGACTGAGGTGGGAGA TAAAATGTTAGGCTGCAGTGGCTCATGCCTGT_ATCCCCCCAGTTTGGGAGACTGAGGTGGGAGA TA T SRGN Ensembl:ENSG00000122862 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs931483810 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_17559311 RMVar_hsa_circ_122072,RMVar_hsa_circ_143977 22311 RMVar_ID_22311 Human_SNP_ID_436625611 A-to-I Human chr10 + 69100843 69100843 69100843 GGTATGTTTCTTCTCCTTACTCCCTGCCTGGGATGGCACCTTGGGCAGGACTCTGTTTTGCCCAT GGTATGTTTCTTCTCCTTACTCCCTGCCTGGGGTGGCACCTTGGGCAGGACTCTGTTTTGCCCAT A G SRGN Ensembl:ENSG00000122862 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2008541 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2102,GWAS_ID_2103 RMVar_hsa_circ_122072,RMVar_hsa_circ_143977 22312 RMVar_ID_22312 Human_SNP_ID_436638970 A-to-I Human chr10 + 69153552 69153552 69153552 TTTTTTTTTTAGTAGAGACGGAGCCTTGCTATATTGTCCAAGCTCGTCTTGAACTCCTGACCTTA TTTTTTTTTTAGTAGAGACGGAGCCTTGCTATGTTGTCCAAGCTCGTCTTGAACTCCTGACCTTA A G VPS26A Ensembl:ENSG00000122958 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs914397901 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58789 22313 RMVar_ID_22313 Human_SNP_ID_436639276 A-to-I Human chr10 + 69154846 69154845 69154847 ATAATCATGCACTGTACTCCAGCCTGGGTGACAGAGTGAGACTCTGTCTCTTAAAATATGTGTGT ATAATCATGCACTGTACTCCAGCCTGGGTGAC__AGTGAGACTCTGTCTCTTAAAATATGTGTGT CAG C VPS26A Ensembl:ENSG00000122958 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs780317612 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_58789 22314 RMVar_ID_22314 Human_SNP_ID_436639277 A-to-I Human chr10 + 69154846 69154846 69154846 ATAATCATGCACTGTACTCCAGCCTGGGTGACAGAGTGAGACTCTGTCTCTTAAAATATGTGTGT ATAATCATGCACTGTACTCCAGCCTGGGTGACTGAGTGAGACTCTGTCTCTTAAAATATGTGTGT A T VPS26A Ensembl:ENSG00000122958 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1361990856 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58789 22315 RMVar_ID_22315 Human_SNP_ID_436641794 A-to-I Human chr10 + 69165865 69165865 69165865 CTACTTGGGAGGCTGAGGCAGAAGGATTGCTTAAGCCCAGGAGGTTGAGGCTGCGGCAAGCCATG CTACTTGGGAGGCTGAGGCAGAAGGATTGCTTGAGCCCAGGAGGTTGAGGCTGCGGCAAGCCATG A G VPS26A Ensembl:ENSG00000122958 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs990718521 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58789,RMVar_hsa_circ_143982,RMVar_hsa_circ_337881,RMVar_hsa_circ_373639,RMVar_hsa_circ_143981,RMVar_hsa_circ_143983,RMVar_hsa_circ_316901 22316 RMVar_ID_22316 Human_SNP_ID_436649477 A-to-I Human chr10 + 69196411 69196411 69196411 TACTCCAGAGGCTGAGGCACAAGAATCACTTGAGCCTGGAAAGGAGATATTGCAGTGAACCACAG TACTCCAGAGGCTGAGGCACAAGAATCACTTGCGCCTGGAAAGGAGATATTGCAGTGAACCACAG A C SUPV3L1 Ensembl:ENSG00000156502 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs544568295 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11405644 RMVar_hsa_circ_45786,RMVar_hsa_circ_143986,RMVar_hsa_circ_84183,RMVar_hsa_circ_332316,RMVar_hsa_circ_82828,RMVar_hsa_circ_53347,RMVar_hsa_circ_15560,RMVar_hsa_circ_143993,RMVar_hsa_circ_60056,RMVar_hsa_circ_287853,RMVar_hsa_circ_114565,RMVar_hsa_circ_143994,RMVar_hsa_circ_143995,RMVar_hsa_circ_143999,RMVar_hsa_circ_289400,RMVar_hsa_circ_306714,RMVar_hsa_circ_6403,RMVar_hsa_circ_375261,RMVar_hsa_circ_304625,RMVar_hsa_circ_144000,RMVar_hsa_circ_143997,RMVar_hsa_circ_143998 22317 RMVar_ID_22317 Human_SNP_ID_436651599 A-to-I Human chr10 + 69205508 69205508 69205508 GCGATCCTTCCACCTCAGCCTCCTGAGTAGCTAGGACTACAGGTGTGCGCCATGATGCGTGGTGT GCGATCCTTCCACCTCAGCCTCCTGAGTAGCTGGGACTACAGGTGTGCGCCATGATGCGTGGTGT A G SUPV3L1 Ensembl:ENSG00000156502 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs768315025 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114565,RMVar_hsa_circ_143995,RMVar_hsa_circ_32461 22318 RMVar_ID_22318 Human_SNP_ID_436682930 A-to-I Human chr10 + 69325893 69325893 69325893 GTCTTACTCTGTCGCCTGGGTTGTAGTACAGTAGCACGATCTCACCTCCCTGCAACCTCTGCCTG GTCTTACTCTGTCGCCTGGGTTGTAGTACAGTGGCACGATCTCACCTCCCTGCAACCTCTGCCTG A G HK1 Ensembl:ENSG00000156515 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1381272032 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5647,RMVar_hsa_circ_351104,RMVar_hsa_circ_54196,RMVar_hsa_circ_57635 22319 RMVar_ID_22319 Human_SNP_ID_436684441 A-to-I Human chr10 + 69331753 69331753 69331753 AAAACGTCAGCTGGGCATGGTGGCACACATCTATGGTCCCAGCCACTTGGGAGTCTGAGGTGAGA AAAACGTCAGCTGGGCATGGTGGCACACATCTGTGGTCCCAGCCACTTGGGAGTCTGAGGTGAGA A G HK1 Ensembl:ENSG00000156515 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978659007 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5647,RMVar_hsa_circ_351104,RMVar_hsa_circ_54196,RMVar_hsa_circ_57635 22320 RMVar_ID_22320 Human_SNP_ID_436696440 A-to-I Human chr10 + 69381165 69381165 69381165 AATCATACACAGCTGGGTGTGGTGGTGTGCCTATAATCCCAGTTACTTGGGAGGCTGAGGTGGGA AATCATACACAGCTGGGTGTGGTGGTGTGCCTGTAATCCCAGTTACTTGGGAGGCTGAGGTGGGA A G HK1 Ensembl:ENSG00000156515 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs997712283 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116921,RMVar_hsa_circ_47729,RMVar_hsa_circ_144006,RMVar_hsa_circ_97069,RMVar_hsa_circ_120740,RMVar_hsa_circ_144011,RMVar_hsa_circ_15250,RMVar_hsa_circ_144013,RMVar_hsa_circ_144014,RMVar_hsa_circ_117876,RMVar_hsa_circ_33216 22321 RMVar_ID_22321 Human_SNP_ID_436698029 A-to-I Human chr10 + 69387320 69387320 69387320 TTTTAAAGTTTCCTTTTTTGAGACAGGGTCTTACTCTGTCACCCAGGCTGGAGTGCAGTGGAGCA TTTTAAAGTTTCCTTTTTTGAGACAGGGTCTTGCTCTGTCACCCAGGCTGGAGTGCAGTGGAGCA A G HK1 Ensembl:ENSG00000156515 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909393706 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116921,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_372687,RMVar_hsa_circ_64188,RMVar_hsa_circ_337171,RMVar_hsa_circ_41688,RMVar_hsa_circ_95354,RMVar_hsa_circ_312746,RMVar_hsa_circ_356433,RMVar_hsa_circ_144019 22322 RMVar_ID_22322 Human_SNP_ID_436868967 A-to-I Human chr10 - 70084717 70084717 70084717 TGTGCCTGTAGTTCCACCTACTTAGGGGGCTAAGGCAGGAGGATTGCTTGAGCTCAGGAGGTCTA TGTGCCTGTAGTTCCACCTACTTAGGGGGCTAGGGCAGGAGGATTGCTTGAGCTCAGGAGGTCTA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048212505 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_144031,RMVar_hsa_circ_144030 22323 RMVar_ID_22323 Human_SNP_ID_436884664 A-to-I Human chr10 - 70147982 70147982 70147982 CCCAGCGACTGGGGAGGCTGAGGCAGGAGAATAGCGTGAACCCAGGAGGCGGAGTTTGCAGTGAG CCCAGCGACTGGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCAGGAGGCGGAGTTTGCAGTGAG T C SAR1A Ensembl:ENSG00000079332 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215659712 Functional Loss SNV dbSNP153 33..33 33 - - - 22324 RMVar_ID_22324 Human_SNP_ID_436888542 A-to-I Human chr10 + 70163670 70163670 70163670 CAGAGTGGTTGTGTGGTTGCGTCTCGGAAACCAGTAGCACTTGCAGCATGGCTGACCAACTGACT CAGAGTGGTTGTGTGGTTGCGTCTCGGAAACCGGTAGCACTTGCAGCATGGCTGACCAACTGACT A G - - Other Unknown GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs879112930 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1159570,Human_RBP_ID_1449180 22325 RMVar_ID_22325 Human_SNP_ID_436888544 A-to-I Human chr10 + 70163676 70163676 70163676 GGTTGTGTGGTTGCGTCTCGGAAACCAGTAGCACTTGCAGCATGGCTGACCAACTGACTGAGGAG GGTTGTGTGGTTGCGTCTCGGAAACCAGTAGCGCTTGCAGCATGGCTGACCAACTGACTGAGGAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879042753 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1159570,Human_RBP_ID_1449180 22326 RMVar_ID_22326 Human_SNP_ID_436888559 A-to-I Human chr10 - 70163731 70163730 70163731 TTCCATCACCATCTTTGTCAAATAGTGAAAAAACTTCTTTGAATTCTACAATCTGCTCCTCAGTC TTCCATCACCATCTTTGTCAAATAGTGAAAAA_CTTCTTTGAATTCTACAATCTGCTCCTCAGTC GT G SAR1A Ensembl:ENSG00000079332 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277164443 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_105466,RMVar_hsa_circ_144047 22327 RMVar_ID_22327 Human_SNP_ID_436888560 A-to-I Human chr10 - 70163731 70163731 70163731 TTCCATCACCATCTTTGTCAAATAGTGAAAAAACTTCTTTGAATTCTACAATCTGCTCCTCAGTC TTCCATCACCATCTTTGTCAAATAGTGAAAAAGCTTCTTTGAATTCTACAATCTGCTCCTCAGTC T C SAR1A Ensembl:ENSG00000079332 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879068471 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105466,RMVar_hsa_circ_144047 22328 RMVar_ID_22328 Human_SNP_ID_436888611 A-to-I Human chr10 - 70163953 70163953 70163953 AATATAGCCATTGCCATCCTTATCAAACACACAGAATGTTTCTCTAATTTCTTCTTCACTGTCTG AATATAGCCATTGCCATCCTTATCAAACACACGGAATGTTTCTCTAATTTCTTCTTCACTGTCTG T C SAR1A Ensembl:ENSG00000079332 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879030462 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3355555 RMVar_hsa_circ_105466,RMVar_hsa_circ_144047 22329 RMVar_ID_22329 Human_SNP_ID_436900945 A-to-I Human chr10 - 70215663 70215663 70215663 CAGTCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCTAGGCATGGTGG CAGTCTGGCCAACATGGTGAAACCCCATCTCTGCTAAAAATACAAAAATTAGCTAGGCATGGTGG T C PPA1 Ensembl:ENSG00000180817 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs907307098 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_144049,RMVar_hsa_circ_114183,RMVar_hsa_circ_102991,RMVar_hsa_circ_144050,RMVar_hsa_circ_144051,RMVar_hsa_circ_91617,RMVar_hsa_circ_378296,RMVar_hsa_circ_144057,RMVar_hsa_circ_144058,RMVar_hsa_circ_103205,RMVar_hsa_circ_265215,RMVar_hsa_circ_346134,RMVar_hsa_circ_144060,RMVar_hsa_circ_280611,RMVar_hsa_circ_144063,RMVar_hsa_circ_144064,RMVar_hsa_circ_272487,RMVar_hsa_circ_144066,RMVar_hsa_circ_118844 22330 RMVar_ID_22330 Human_SNP_ID_436903059 A-to-I Human chr10 - 70222079 70222073 70222080 CGCCCACCTCGGCCTCCCAAAGTGCTATGATTACAGGTGTGAGCCACCACCCCCCGGCCTCACCC CGCCCACCTCGGCCTCCCAAAGTGCTATGAT_______GTGAGCCACCACCCCCCGGCCTCACCC CACCTGTA C PPA1 Ensembl:ENSG00000180817 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1472179513 Functional Loss DEL dbSNP153 32..38 33 - - - RMVar_hsa_circ_91617,RMVar_hsa_circ_144058 22331 RMVar_ID_22331 Human_SNP_ID_436904919 A-to-I Human chr10 - 70230047 70230047 70230047 AAAATTAGCCGGGCATGGTGGCATGTGTCTGTAGTCTCAGCTACTTGGAAGGCTGAGGTGAGAGG AAAATTAGCCGGGCATGGTGGCATGTGTCTGTGGTCTCAGCTACTTGGAAGGCTGAGGTGAGAGG T C PPA1 Ensembl:ENSG00000180817 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1428752904 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91617,RMVar_hsa_circ_144058 22332 RMVar_ID_22332 Human_SNP_ID_436904934 A-to-I Human chr10 - 70230091 70230091 70230091 CAGCCTGGGCAACATGGTGAAACCCTGTCTCTACAAAAAATACAAAAATTAGCCGGGCATGGTGG CAGCCTGGGCAACATGGTGAAACCCTGTCTCTCCAAAAAATACAAAAATTAGCCGGGCATGGTGG T G PPA1 Ensembl:ENSG00000180817 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1186772220 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91617,RMVar_hsa_circ_144058 22333 RMVar_ID_22333 Human_SNP_ID_436905244 A-to-I Human chr10 - 70231443 70231443 70231443 CCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCACTTGCCACCATGCCTGACTAATTTTTGT CCTGCCTCAGCCTCCCAAGTAGCTGGGATTACGGGCACTTGCCACCATGCCTGACTAATTTTTGT T C PPA1 Ensembl:ENSG00000180817 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1046070238 Functional Loss SNV dbSNP153 33..33 33 - - - 22334 RMVar_ID_22334 Human_SNP_ID_436948506 A-to-I Human chr10 + 70404398 70404398 70404398 CCCGCCGGACAAAGCCGAGAGCCCGCGCCCACAGCCATGTCCTCGTCAGCCGGCAGCGGCCACCA CCCGCCGGACAAAGCCGAGAGCCCGCGCCCACGGCCATGTCCTCGTCAGCCGGCAGCGGCCACCA A G EIF4EBP2 Ensembl:ENSG00000148730 Protein coding 5'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs892367854 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22029813 RMVar_hsa_circ_98215,RMVar_hsa_circ_144070 22335 RMVar_ID_22335 Human_SNP_ID_436949033 A-to-I Human chr10 + 70406013 70406009 70406013 CCAACTCGTGTTTGAGCATGGTACAGGGTCTCACTCTGTCGCCCAGGCTGGAGTACAGTGGCACG CCAACTCGTGTTTGAGCATGGTACAGGGT____CTCTGTCGCCCAGGCTGGAGTACAGTGGCACG TCTCA T EIF4EBP2 Ensembl:ENSG00000148730 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1457661851 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_98215,RMVar_hsa_circ_144070 22336 RMVar_ID_22336 Human_SNP_ID_436951751 A-to-I Human chr10 + 70415145 70415145 70415145 GCACTTCTGCCCTCTAGCTTGGACGACAGAGCAAGACCCTCTCTCGAAAAAAAAAAAAAAGAAAA GCACTTCTGCCCTCTAGCTTGGACGACAGAGCGAGACCCTCTCTCGAAAAAAAAAAAAAAGAAAA A G EIF4EBP2 Ensembl:ENSG00000148730 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs545276182 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98215,RMVar_hsa_circ_144070 22337 RMVar_ID_22337 Human_SNP_ID_437055317 A-to-I Human chr10 + 70816826 70816826 70816826 CTGGTTCCCTTTTACAGAGTCTGAAAAAGGGGAGCGCGGAGAGGAGGCTGGAAGAGGAAGATGCC CTGGTTCCCTTTTACAGAGTCTGAAAAAGGGGTGCGCGGAGAGGAGGCTGGAAGAGGAAGATGCC A T SGPL1 Ensembl:ENSG00000166224 Protein coding 5'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs765351111 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_864072,Human_RBP_ID_4125742,Human_RBP_ID_18468842,Human_RBP_ID_18970788 Human_Splice_Rec_1143290,Human_Splice_Rec_1143291,Human_Splice_Rec_1143318,Human_Splice_Rec_1143319 Human_miRNA_ID_2973730,Human_miRNA_ID_3006914 RMVar_hsa_circ_37814,RMVar_hsa_circ_118306,RMVar_hsa_circ_62761,RMVar_hsa_circ_144089 22338 RMVar_ID_22338 Human_SNP_ID_437304246 A-to-I Human chr10 - 71809372 71809371 71809372 GAGTTTGAGACTAGCCTGGCCAACATGATGAAACCCCATCTGTACTAAAAATACAAAATCTAGCC GAGTTTGAGACTAGCCTGGCCAACATGATGAA_CCCCATCTGTACTAAAAATACAAAATCTAGCC GT G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1233043437 Functional Loss DEL dbSNP153 33..33 33 - - - 22339 RMVar_ID_22339 Human_SNP_ID_437358207 A-to-I Human chr10 + 72012611 72012611 72012611 GAAGCCAGATCTCAAGGGCTGATACCTGAGGCAAGGAGAGCTAAGGGGAGAGAAATTGGGGCTGA GAAGCCAGATCTCAAGGGCTGATACCTGAGGCTAGGAGAGCTAAGGGGAGAGAAATTGGGGCTGA A T CHST3 Ensembl:ENSG00000122863 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs982233347 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5995321,Human_RBP_ID_8338246,Human_RBP_ID_18243672 RMVar_hsa_circ_127679,RMVar_hsa_circ_144157 22340 RMVar_ID_22340 Human_SNP_ID_437378595 A-to-I Human chr10 - 72093222 72093222 72093222 TAGTGGCATGCGACTGTAGTCCCAGCTACTTCAGAGGCTGAGGTGGGATCAATTGAGCCCAGGAG TAGTGGCATGCGACTGTAGTCCCAGCTACTTCCGAGGCTGAGGTGGGATCAATTGAGCCCAGGAG T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1487750495 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24829831 22341 RMVar_ID_22341 Human_SNP_ID_437378710 A-to-I Human chr10 - 72093712 72093712 72093712 GAAACCAGAGGTTCGCTTGAGGCCGGGAGTCCAAGACCAGCATCGGCAAACTAGTAAGACCCCAT GAAACCAGAGGTTCGCTTGAGGCCGGGAGTCCGAGACCAGCATCGGCAAACTAGTAAGACCCCAT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1330465897 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100809,RMVar_hsa_circ_144158 22342 RMVar_ID_22342 Human_SNP_ID_437387618 A-to-I Human chr10 - 72131247 72131247 72131247 GCTCAGCTAATTTTCGTATTTTTAGTAGAGACAGGGTTTCACCATCTTGGCCAGGCTGATCTTGA GCTCAGCTAATTTTCGTATTTTTAGTAGAGACGGGGTTTCACCATCTTGGCCAGGCTGATCTTGA T C ASCC1 Ensembl:ENSG00000138303 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1265774542 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_144159,RMVar_hsa_circ_93152,RMVar_hsa_circ_99451,RMVar_hsa_circ_144160,RMVar_hsa_circ_144163,RMVar_hsa_circ_286656,RMVar_hsa_circ_332934,RMVar_hsa_circ_344363,RMVar_hsa_circ_367403,RMVar_hsa_circ_310390,RMVar_hsa_circ_144164,RMVar_hsa_circ_144161,RMVar_hsa_circ_144162 22343 RMVar_ID_22343 Human_SNP_ID_437391493 A-to-I Human chr10 - 72147391 72147391 72147391 AAAATTAGCTGGGTGTGGTGGCTCATGCCTGTAACGCAGCTGCTCGGGAGGCTGAGGCAGGAGAA AAAATTAGCTGGGTGTGGTGGCTCATGCCTGTTACGCAGCTGCTCGGGAGGCTGAGGCAGGAGAA T A ASCC1 Ensembl:ENSG00000138303 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs192278351 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24829939 RMVar_hsa_circ_24542,RMVar_hsa_circ_93152,RMVar_hsa_circ_144160,RMVar_hsa_circ_144163,RMVar_hsa_circ_332934,RMVar_hsa_circ_344363,RMVar_hsa_circ_367403,RMVar_hsa_circ_310390,RMVar_hsa_circ_144164,RMVar_hsa_circ_144162,RMVar_hsa_circ_97494,RMVar_hsa_circ_144165 22344 RMVar_ID_22344 Human_SNP_ID_437401498 A-to-I Human chr10 - 72188158 72188158 72188158 GCCACAATCATGCCACTGCACTCCAGCCTGACAGAGCGAGACTGTCTCAAAAAAAAAAAAAAAAA GCCACAATCATGCCACTGCACTCCAGCCTGACGGAGCGAGACTGTCTCAAAAAAAAAAAAAAAAA T C ASCC1 Ensembl:ENSG00000138303 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1166526308 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93152,RMVar_hsa_circ_144160,RMVar_hsa_circ_144163,RMVar_hsa_circ_344363,RMVar_hsa_circ_310390,RMVar_hsa_circ_144164,RMVar_hsa_circ_97494,RMVar_hsa_circ_30480,RMVar_hsa_circ_292082,RMVar_hsa_circ_144165,RMVar_hsa_circ_296758,RMVar_hsa_circ_72540,RMVar_hsa_circ_144166,RMVar_hsa_circ_321859,RMVar_hsa_circ_374400 22345 RMVar_ID_22345 Human_SNP_ID_437410770 A-to-I Human chr10 + 72220218 72220218 72220218 AGGCATGGTGGTGCATGCCTGTAATCCCAGCTACTCGGGAGGCTGAAGCAGGAGAATCGCTTAAA AGGCATGGTGGTGCATGCCTGTAATCCCAGCTGCTCGGGAGGCTGAAGCAGGAGAATCGCTTAAA A G ANAPC16 Ensembl:ENSG00000166295 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893133704 Functional Loss SNV dbSNP153 33..33 33 - - - 22346 RMVar_ID_22346 Human_SNP_ID_437410782 A-to-I Human chr10 + 72220248 72220248 72220248 CTACTCGGGAGGCTGAAGCAGGAGAATCGCTTAAATCCGGGAGGCAGAGGTTGCTGTGAGCCGAG CTACTCGGGAGGCTGAAGCAGGAGAATCGCTTGAATCCGGGAGGCAGAGGTTGCTGTGAGCCGAG A G ANAPC16 Ensembl:ENSG00000166295 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs12766396 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24830132 22347 RMVar_ID_22347 Human_SNP_ID_437410789 A-to-I Human chr10 + 72220261 72220261 72220261 TGAAGCAGGAGAATCGCTTAAATCCGGGAGGCAGAGGTTGCTGTGAGCCGAGATCGCGCCATTTC TGAAGCAGGAGAATCGCTTAAATCCGGGAGGCGGAGGTTGCTGTGAGCCGAGATCGCGCCATTTC A G ANAPC16 Ensembl:ENSG00000166295 Protein coding intron GSE47997;GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line - 23474544,24183664,29129909,29796672,31158229 RNA-Seq:(High) rs1405210641 Functional Loss SNV dbSNP153 33..33 33 - - - 22348 RMVar_ID_22348 Human_SNP_ID_437410866 A-to-I Human chr10 + 72220395 72220395 72220395 AGTTTCAGCCAGGCATGGTGGGTCACACCTGTAATCCCAACACTTTGGGAGGCCAGGGTGGGAGA AGTTTCAGCCAGGCATGGTGGGTCACACCTGTGATCCCAACACTTTGGGAGGCCAGGGTGGGAGA A G ANAPC16 Ensembl:ENSG00000166295 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs535699961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225933 22349 RMVar_ID_22349 Human_SNP_ID_437410885 A-to-I Human chr10 + 72220490 72220490 72220490 TAGGGGCAACATGGTGAGAAGTTGTCTCTACTAAAAGTAAAAAGAATTAGCTGGGCATGGTGGCA TAGGGGCAACATGGTGAGAAGTTGTCTCTACTTAAAGTAAAAAGAATTAGCTGGGCATGGTGGCA A T ANAPC16 Ensembl:ENSG00000166295 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1275198254 Functional Loss SNV dbSNP153 33..33 33 - - - 22350 RMVar_ID_22350 Human_SNP_ID_437411065 A-to-I Human chr10 + 72221021 72221021 72221021 TCACTGCAACCTCCACCTCCCGAGTTCAAGCTATTCTCCTGCCTCAGCCTTCCAAGTAGCTGGGA TCACTGCAACCTCCACCTCCCGAGTTCAAGCTGTTCTCCTGCCTCAGCCTTCCAAGTAGCTGGGA A G ANAPC16 Ensembl:ENSG00000166295 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs927487125 Functional Loss SNV dbSNP153 33..33 33 - - - 22351 RMVar_ID_22351 Human_SNP_ID_437411352 A-to-I Human chr10 + 72221988 72221988 72221988 CTGACCTCGTGATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCA CTGACCTCGTGATCCACCCGCCTCGGCCTCCCGAAGTGCTGGGATTACAGGTGTGAGCCACCGCA A G ANAPC16 Ensembl:ENSG00000166295 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1319604355 Functional Loss SNV dbSNP153 33..33 33 - - - 22352 RMVar_ID_22352 Human_SNP_ID_437411437 A-to-I Human chr10 + 72222262 72222262 72222262 CAACATGGCGAAACCCTGTCTCAACTAAAAATACAAAAATTAGCTGGGCGTGGTGGCACGCGCCT CAACATGGCGAAACCCTGTCTCAACTAAAAATTCAAAAATTAGCTGGGCGTGGTGGCACGCGCCT A T ANAPC16 Ensembl:ENSG00000166295 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1242335125 Functional Loss SNV dbSNP153 33..33 33 - - - 22353 RMVar_ID_22353 Human_SNP_ID_437411454 A-to-I Human chr10 + 72222307 72222307 72222307 GGGCGTGGTGGCACGCGCCTGTAGTCCCAGCTACTCAGGAGGTTGAGGCAGGAGAATCGCTTGAA GGGCGTGGTGGCACGCGCCTGTAGTCCCAGCTGCTCAGGAGGTTGAGGCAGGAGAATCGCTTGAA A G ANAPC16 Ensembl:ENSG00000166295 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1452353817 Functional Loss SNV dbSNP153 33..33 33 - - - 22354 RMVar_ID_22354 Human_SNP_ID_437411469 A-to-I Human chr10 + 72222350 72222350 72222350 TGAGGCAGGAGAATCGCTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCAGAGATCGCGCCACTGC TGAGGCAGGAGAATCGCTTGAACCTGGGAGGCGGAGGTTGCAGTGAGCAGAGATCGCGCCACTGC A G ANAPC16 Ensembl:ENSG00000166295 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1439145651 Functional Loss SNV dbSNP153 33..33 33 - - - 22355 RMVar_ID_22355 Human_SNP_ID_437411582 A-to-I Human chr10 + 72222623 72222623 72222623 ACGTGGTGAAACCCCGTGCCTACTAAAAATACAAAAATTAGCTGGGCATGGTGGCTCATGCCTGT ACGTGGTGAAACCCCGTGCCTACTAAAAATACGAAAATTAGCTGGGCATGGTGGCTCATGCCTGT A G ANAPC16 Ensembl:ENSG00000166295 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1164480232 Functional Loss SNV dbSNP153 33..33 33 - - - 22356 RMVar_ID_22356 Human_SNP_ID_437411764 A-to-I Human chr10 + 72223163 72223163 72223163 AGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAATGATTCTCTTGCCTCAGCCTCCTGAGTAGCT AGGCTCACTGCAACCTCCGCCTCCCGGGTTCAGATGATTCTCTTGCCTCAGCCTCCTGAGTAGCT A G ANAPC16 Ensembl:ENSG00000166295 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1486524271 Functional Loss SNV dbSNP153 33..33 33 - - - 22357 RMVar_ID_22357 Human_SNP_ID_437412547 A-to-I Human chr10 + 72226093 72226093 72226093 GCTGTAGTGCAGTGGCTCGATCTTGGCTCACTACAACCTCTGCCTCCCGGGTTCAAGTGATTCTC GCTGTAGTGCAGTGGCTCGATCTTGGCTCACTGCAACCTCTGCCTCCCGGGTTCAAGTGATTCTC A G ANAPC16 Ensembl:ENSG00000166295 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025042792 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_286353,RMVar_hsa_circ_144174 22358 RMVar_ID_22358 Human_SNP_ID_437412565 A-to-I Human chr10 + 72226199 72226199 72226199 CACCACACCTGGCTAATTTTTTTAATATTTTTAATAGAGGCAGGGTTTCGCCATGTTGCCCAGGC CACCACACCTGGCTAATTTTTTTAATATTTTTCATAGAGGCAGGGTTTCGCCATGTTGCCCAGGC A C ANAPC16 Ensembl:ENSG00000166295 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs961256349 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24830180 RMVar_hsa_circ_286353,RMVar_hsa_circ_144174 22359 RMVar_ID_22359 Human_SNP_ID_437412578 A-to-I Human chr10 + 72226254 72226254 72226254 TTGCCCAGGCTGAGCTTGAACTCCTGACCTCAAATGATCTGCCCACCTCAGCCTCCCAAAGTGCT TTGCCCAGGCTGAGCTTGAACTCCTGACCTCATATGATCTGCCCACCTCAGCCTCCCAAAGTGCT A T ANAPC16 Ensembl:ENSG00000166295 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs926023267 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_286353,RMVar_hsa_circ_144174 22360 RMVar_ID_22360 Human_SNP_ID_437412618 A-to-I Human chr10 + 72226445 72226445 72226445 CCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGCAGATTGCTTGAACCCAGGAGTTTGAGACC CCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGCAGATTGCTTGAACCCAGGAGTTTGAGACC A G ANAPC16 Ensembl:ENSG00000166295 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs888168045 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_286353,RMVar_hsa_circ_144174 22361 RMVar_ID_22361 Human_SNP_ID_437412644 A-to-I Human chr10 + 72226552 72226552 72226552 AAAATTAGCTGGGTGTGGTGGCACGTGGCTGTAGTCCCAGCTACTTAGGAAGGTGAGGTGGGAGG AAAATTAGCTGGGTGTGGTGGCACGTGGCTGTGGTCCCAGCTACTTAGGAAGGTGAGGTGGGAGG A G ANAPC16 Ensembl:ENSG00000166295 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1365915120 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_286353,RMVar_hsa_circ_144174 22362 RMVar_ID_22362 Human_SNP_ID_437412645 A-to-I Human chr10 + 72226566 72226566 72226566 GTGGTGGCACGTGGCTGTAGTCCCAGCTACTTAGGAAGGTGAGGTGGGAGGTTCACCTGAGCCTG GTGGTGGCACGTGGCTGTAGTCCCAGCTACTTCGGAAGGTGAGGTGGGAGGTTCACCTGAGCCTG A C ANAPC16 Ensembl:ENSG00000166295 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs943362780 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_286353,RMVar_hsa_circ_144174 22363 RMVar_ID_22363 Human_SNP_ID_437413795 A-to-I Human chr10 + 72231336 72231336 72231336 GAAGCAGGAAGACTGCTTGAGCCCAGGAGTTCAAGACTGACCTGGGCAACATGGTGAAACCCCAT GAAGCAGGAAGACTGCTTGAGCCCAGGAGTTCCAGACTGACCTGGGCAACATGGTGAAACCCCAT A C ANAPC16 Ensembl:ENSG00000166295 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs925249137 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119478,RMVar_hsa_circ_144176 22364 RMVar_ID_22364 Human_SNP_ID_437413796 A-to-I Human chr10 + 72231336 72231336 72231336 GAAGCAGGAAGACTGCTTGAGCCCAGGAGTTCAAGACTGACCTGGGCAACATGGTGAAACCCCAT GAAGCAGGAAGACTGCTTGAGCCCAGGAGTTCGAGACTGACCTGGGCAACATGGTGAAACCCCAT A G ANAPC16 Ensembl:ENSG00000166295 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs925249137 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119478,RMVar_hsa_circ_144176 22365 RMVar_ID_22365 Human_SNP_ID_437414003 A-to-I Human chr10 + 72232022 72232022 72232022 TGGCCTGACCAACATGGAGAAACCCCATCTCTACTAAAAATACAAAATTAGCCAGGCATGGTGGC TGGCCTGACCAACATGGAGAAACCCCATCTCTGCTAAAAATACAAAATTAGCCAGGCATGGTGGC A G ANAPC16 Ensembl:ENSG00000166295 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs556290881 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119478,RMVar_hsa_circ_144176 22366 RMVar_ID_22366 Human_SNP_ID_437414626 A-to-I Human chr10 + 72234071 72234071 72234071 TCTTGTTGCCCAGGCTGTATCGCAATGGCGCGATCTCTGCTCACTGCAACATCCACCTCCCAGGT TCTTGTTGCCCAGGCTGTATCGCAATGGCGCGCTCTCTGCTCACTGCAACATCCACCTCCCAGGT A C ANAPC16 Ensembl:ENSG00000166295 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs898013170 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119478,RMVar_hsa_circ_144176 22367 RMVar_ID_22367 Human_SNP_ID_437414656 A-to-I Human chr10 + 72234229 72234229 72234229 GGGGTTTCACCATGTTGACCAGGCTAGTCTCGAACTTCTGACCTCAGGTGATCCACCTGCCTCAG GGGGTTTCACCATGTTGACCAGGCTAGTCTCGCACTTCTGACCTCAGGTGATCCACCTGCCTCAG A C ANAPC16 Ensembl:ENSG00000166295 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1168682596 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119478,RMVar_hsa_circ_144176 22368 RMVar_ID_22368 Human_SNP_ID_437414658 A-to-I Human chr10 + 72234242 72234242 72234242 GTTGACCAGGCTAGTCTCGAACTTCTGACCTCAGGTGATCCACCTGCCTCAGCCTCCCAAATTGC GTTGACCAGGCTAGTCTCGAACTTCTGACCTCGGGTGATCCACCTGCCTCAGCCTCCCAAATTGC A G ANAPC16 Ensembl:ENSG00000166295 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1242985219 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119478,RMVar_hsa_circ_144176 22369 RMVar_ID_22369 Human_SNP_ID_437414665 A-to-I Human chr10 + 72234268 72234268 72234268 GACCTCAGGTGATCCACCTGCCTCAGCCTCCCAAATTGCTGGGATTACAGGCGTGAGCCACCTTG GACCTCAGGTGATCCACCTGCCTCAGCCTCCCGAATTGCTGGGATTACAGGCGTGAGCCACCTTG A G ANAPC16 Ensembl:ENSG00000166295 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs977440757 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119478,RMVar_hsa_circ_144176 22370 RMVar_ID_22370 Human_SNP_ID_437414689 A-to-I Human chr10 + 72234372 72234371 72234373 GTTGCCCAGGTTGGTCTTGAACTCCTGGCCTCAAGAGATCCCCCCAACCTTGGCCTCCAAAGTGC GTTGCCCAGGTTGGTCTTGAACTCCTGGCCTC__GAGATCCCCCCAACCTTGGCCTCCAAAGTGC CAA C ANAPC16 Ensembl:ENSG00000166295 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1051972245 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_119478,RMVar_hsa_circ_144176 22371 RMVar_ID_22371 Human_SNP_ID_437414772 A-to-I Human chr10 + 72234730 72234730 72234730 ATTCTACCTGACGGGAGGTGGTGACCTCATTCAGTCGGTTAAGAGCCTGAGCCCTGTGAAGTTAA ATTCTACCTGACGGGAGGTGGTGACCTCATTCGGTCGGTTAAGAGCCTGAGCCCTGTGAAGTTAA A G ANAPC16 Ensembl:ENSG00000166295 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1043390348 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8172666,Human_RBP_ID_26398363 RMVar_hsa_circ_119478,RMVar_hsa_circ_144176 22372 RMVar_ID_22372 Human_SNP_ID_437414810 A-to-I Human chr10 + 72234949 72234949 72234949 GAGGTGAGTGGATCACTAGAGGTCAGGAGTTCAAGACCAGTCTGGCCGACATGGTGAAACTCAGT GAGGTGAGTGGATCACTAGAGGTCAGGAGTTCGAGACCAGTCTGGCCGACATGGTGAAACTCAGT A G ANAPC16 Ensembl:ENSG00000166295 Protein coding 3'UTR GSE38233;GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,30559470,31158229,31158229,32596459 RNA-Seq:(High) rs1248533670 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23152709,Human_RBP_ID_26398364 RMVar_hsa_circ_119478,RMVar_hsa_circ_144176 22373 RMVar_ID_22373 Human_SNP_ID_437414828 A-to-I Human chr10 + 72235009 72235009 72235009 TCAGTCTCTATTGAAAATACAAAAATTAGCTCAGTGTGGTGGCACACACTTGTAATCCCAGCTAC TCAGTCTCTATTGAAAATACAAAAATTAGCTCGGTGTGGTGGCACACACTTGTAATCCCAGCTAC A G ANAPC16 Ensembl:ENSG00000166295 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs925868284 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119478,RMVar_hsa_circ_144176 22374 RMVar_ID_22374 Human_SNP_ID_437414842 A-to-I Human chr10 + 72235070 72235070 72235070 CTACTCAGGAGGCTGAGGCATGAGAATCGCTTAAACCCAGGAGGCGGAGGTTGCAGTGAGCTGAG CTACTCAGGAGGCTGAGGCATGAGAATCGCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCTGAG A G ANAPC16 Ensembl:ENSG00000166295 Protein coding 3'UTR GSE47997;GSE38233;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;cultured B-cells;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 23474544,24183664,29796672,31158229,31158229 RNA-Seq:(High) rs1198743211 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119478,RMVar_hsa_circ_144176 22375 RMVar_ID_22375 Human_SNP_ID_437414846 A-to-I Human chr10 + 72235076 72235076 72235076 AGGAGGCTGAGGCATGAGAATCGCTTAAACCCAGGAGGCGGAGGTTGCAGTGAGCTGAGATCACA AGGAGGCTGAGGCATGAGAATCGCTTAAACCCGGGAGGCGGAGGTTGCAGTGAGCTGAGATCACA A G ANAPC16 Ensembl:ENSG00000166295 Protein coding 3'UTR GSE47997;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 23474544,31158229,31158229 RNA-Seq:(High) rs1252145100 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119478,RMVar_hsa_circ_144176 22376 RMVar_ID_22376 Human_SNP_ID_437414930 A-to-I Human chr10 + 72235341 72235341 72235341 AGGCGTGGTGGCGGGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGCAGAATCGTTTGAA AGGCGTGGTGGCGGGCGCCTGTAATCCCAGCTGCTCAGGAGGCTGAGGCAGCAGAATCGTTTGAA A G ANAPC16 Ensembl:ENSG00000166295 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1423072332 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119478,RMVar_hsa_circ_144176 22377 RMVar_ID_22377 Human_SNP_ID_437414959 A-to-I Human chr10 + 72235434 72235433 72235435 AGATCGTGCCTGTGTGCTCCAGCCTGAGCAACAAGAGCGAAACTGTCTCAAAAAAAAGAAGAAAA AGATCGTGCCTGTGTGCTCCAGCCTGAGCAAC__GAGCGAAACTGTCTCAAAAAAAAGAAGAAAA CAA C ANAPC16 Ensembl:ENSG00000166295 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1164676884 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_5995977,Human_RBP_ID_18597511,Human_RBP_ID_26398365 RMVar_hsa_circ_119478,RMVar_hsa_circ_144176 22378 RMVar_ID_22378 Human_SNP_ID_437442785 A-to-I Human chr10 - 72339816 72339816 72339816 ATCCCTACTCGGGAAGCTGAGGCATGAGAATCACTTGAACCCAGGAGGCAGAGGTTGTGTTGAGC ATCCCTACTCGGGAAGCTGAGGCATGAGAATCCCTTGAACCCAGGAGGCAGAGGTTGTGTTGAGC T G DNAJB12 Ensembl:ENSG00000148719 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1040359948 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109747,RMVar_hsa_circ_92783,RMVar_hsa_circ_75735,RMVar_hsa_circ_144180,RMVar_hsa_circ_144181,RMVar_hsa_circ_144182 22379 RMVar_ID_22379 Human_SNP_ID_437442803 A-to-I Human chr10 - 72339859 72339859 72339859 TAAACATACAAAAATTAGCTGGGCGTAGTGGCAGGCGCCTTTAATCCCTACTCGGGAAGCTGAGG TAAACATACAAAAATTAGCTGGGCGTAGTGGCGGGCGCCTTTAATCCCTACTCGGGAAGCTGAGG T C DNAJB12 Ensembl:ENSG00000148719 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs999293832 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109747,RMVar_hsa_circ_92783,RMVar_hsa_circ_75735,RMVar_hsa_circ_144180,RMVar_hsa_circ_144181,RMVar_hsa_circ_144182 22380 RMVar_ID_22380 Human_SNP_ID_437444349 A-to-I Human chr10 - 72345417 72345417 72345417 TTTAATTTTTAGTACAGACGGGATTTCACCACATTGGCCAGGCTGGTCTCAAACTCCTGACCTCA TTTAATTTTTAGTACAGACGGGATTTCACCACGTTGGCCAGGCTGGTCTCAAACTCCTGACCTCA T C DNAJB12 Ensembl:ENSG00000148719 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1189662355 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76719,RMVar_hsa_circ_144187 22381 RMVar_ID_22381 Human_SNP_ID_437444454 A-to-I Human chr10 - 72345707 72345707 72345707 TCTTTTGGGGTTTTTTTTTTTGTATTTTTAGTAGAGATGGAGTTTCACCATGTTGGCCGGGCTGG TCTTTTGGGGTTTTTTTTTTTGTATTTTTAGTGGAGATGGAGTTTCACCATGTTGGCCGGGCTGG T C DNAJB12 Ensembl:ENSG00000148719 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs983092099 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76719,RMVar_hsa_circ_144187 22382 RMVar_ID_22382 Human_SNP_ID_437448036 A-to-I Human chr10 - 72360078 72360078 72360078 CCACCTTTGCCTCCCAACGTGCTAAGATTACAAGCATAAGCCACGGCGCCCAGGCTTTGTCTCTC CCACCTTTGCCTCCCAACGTGCTAAGATTACAGGCATAAGCCACGGCGCCCAGGCTTTGTCTCTC T C - - Other Unknown GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1435489290 Functional Loss SNV dbSNP153 33..33 33 - - - 22383 RMVar_ID_22383 Human_SNP_ID_437455089 A-to-I Human chr10 - 72391379 72391379 72391379 AGGCTGGGCTGGAGTGCAGTGGCATGATCTCGACTCACTGCAACCTCCGCCTCCCAGATTCAAGC AGGCTGGGCTGGAGTGCAGTGGCATGATCTCGTCTCACTGCAACCTCCGCCTCCCAGATTCAAGC T A MICU1 Ensembl:ENSG00000107745 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs925601480 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85934,RMVar_hsa_circ_268624,RMVar_hsa_circ_144189,RMVar_hsa_circ_69520 22384 RMVar_ID_22384 Human_SNP_ID_437469919 A-to-I Human chr10 - 72453960 72453960 72453960 GTGGTGGTGTGCATCTGCAATCCCAGCTACTCAGGAGGCTGAGGCAAGAAAATCGCTTGAACCAG GTGGTGGTGTGCATCTGCAATCCCAGCTACTCGGGAGGCTGAGGCAAGAAAATCGCTTGAACCAG T C MICU1 Ensembl:ENSG00000107745 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs754431490 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85934,RMVar_hsa_circ_144189,RMVar_hsa_circ_292696,RMVar_hsa_circ_38125 22385 RMVar_ID_22385 Human_SNP_ID_437488180 A-to-I Human chr10 - 72532271 72532271 72532271 CTCTGTCGCCTGGGCTGGAGTGCAGTGGAGCAATCTCGGCTCACTGCAAGCTCCACCTCCCGGGT CTCTGTCGCCTGGGCTGGAGTGCAGTGGAGCAGTCTCGGCTCACTGCAAGCTCCACCTCCCGGGT T C MICU1 Ensembl:ENSG00000107745 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1236673952 Functional Loss SNV dbSNP153 33..33 33 - - - 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 22386 RMVar_ID_22386 Human_SNP_ID_437504657 A-to-I Human chr10 - 72602442 72602442 72602442 GGTTGTATGAATTTTTTTTTTTTTGAGACAGAATCTCGCTTTGTTGCCCAGGCTGGAGTACAGTG GGTTGTATGAATTTTTTTTTTTTTGAGACAGAGTCTCGCTTTGTTGCCCAGGCTGGAGTACAGTG T C MICU1 Ensembl:ENSG00000107745 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1431348502 Functional Loss SNV dbSNP153 33..33 33 - - - 22387 RMVar_ID_22387 Human_SNP_ID_437507802 A-to-I Human chr10 - 72615226 72615226 72615226 GTAATTCCAATTACTGGGGAGGCTGAGGCACAAGTATCACTTGAGCCCAGGAGGCAGAGGTTGCG GTAATTCCAATTACTGGGGAGGCTGAGGCACAGGTATCACTTGAGCCCAGGAGGCAGAGGTTGCG T C MICU1 Ensembl:ENSG00000107745 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs555663132 Functional Loss SNV dbSNP153 33..33 33 - - - 22388 RMVar_ID_22388 Human_SNP_ID_437509089 A-to-I Human chr10 - 72621054 72621054 72621054 TTCATCATTAAAACAATTTTTTTTTCTGTAGAAACGGGGTCTCACTATGTTGCCCAGGGTGGTCT TTCATCATTAAAACAATTTTTTTTTCTGTAGAGACGGGGTCTCACTATGTTGCCCAGGGTGGTCT T C MICU1 Ensembl:ENSG00000107745 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1422040089 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11418750 22389 RMVar_ID_22389 Human_SNP_ID_437532821 A-to-I Human chr10 + 72717359 72717359 72717359 TCGGCTCACTGCAACCTCTACCTCCCGAGTTCAAGCAATTCTCCTACCTCAGCCTCCTAAGTAGC TCGGCTCACTGCAACCTCTACCTCCCGAGTTCTAGCAATTCTCCTACCTCAGCCTCCTAAGTAGC A T MCU Ensembl:ENSG00000156026 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs759519358 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_308267,RMVar_hsa_circ_305538,RMVar_hsa_circ_344394,RMVar_hsa_circ_108317,RMVar_hsa_circ_144203,RMVar_hsa_circ_144205,RMVar_hsa_circ_144206,RMVar_hsa_circ_144204,RMVar_hsa_circ_311083,RMVar_hsa_circ_144202 22390 RMVar_ID_22390 Human_SNP_ID_437536719 A-to-I Human chr10 + 72734726 72734726 72734726 GCCTTGACCTCCCAGGCTCAAGCAATCCTCCCACCTCTGCCTCCCAAGTAGCTAGGACCAAAGGC GCCTTGACCTCCCAGGCTCAAGCAATCCTCCCCCCTCTGCCTCCCAAGTAGCTAGGACCAAAGGC A C MCU Ensembl:ENSG00000156026 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs961045413 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_308267,RMVar_hsa_circ_305538,RMVar_hsa_circ_344394,RMVar_hsa_circ_108317,RMVar_hsa_circ_144203,RMVar_hsa_circ_144205,RMVar_hsa_circ_144204,RMVar_hsa_circ_311083,RMVar_hsa_circ_144202 22391 RMVar_ID_22391 Human_SNP_ID_437538267 A-to-I Human chr10 + 72741849 72741848 72741849 AGGAGATCGAGACCATCCTGGCTAAGACGGTGAAACCCTGTCTCTACTAAAAATACCAAAAATTA AGGAGATCGAGACCATCCTGGCTAAGACGGTG_AACCCTGTCTCTACTAAAAATACCAAAAATTA GA G MCU Ensembl:ENSG00000156026 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs773066156 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_308267,RMVar_hsa_circ_305538,RMVar_hsa_circ_108317,RMVar_hsa_circ_144203,RMVar_hsa_circ_144204,RMVar_hsa_circ_311083,RMVar_hsa_circ_144202 22392 RMVar_ID_22392 Human_SNP_ID_437539816 A-to-I Human chr10 + 72748282 72748282 72748282 GTTGGCCAGTCTGTTCTTGAACTCCTGACTTCAGGTGATCCGCCCGCCTTGGCCTCCCGAAGTGC GTTGGCCAGTCTGTTCTTGAACTCCTGACTTCGGGTGATCCGCCCGCCTTGGCCTCCCGAAGTGC A G MCU Ensembl:ENSG00000156026 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1480096181 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_308267,RMVar_hsa_circ_305538,RMVar_hsa_circ_108317,RMVar_hsa_circ_144203,RMVar_hsa_circ_311083,RMVar_hsa_circ_144202 22393 RMVar_ID_22393 Human_SNP_ID_437543951 A-to-I Human chr10 + 72766082 72766082 72766082 AGAGATGTGGGGGTCTCACTGTTTTGCGGGCTAGTCTTGAACACCTGGCCTCAAGCAGTCCTCTC AGAGATGTGGGGGTCTCACTGTTTTGCGGGCTGGTCTTGAACACCTGGCCTCAAGCAGTCCTCTC A G MCU Ensembl:ENSG00000156026 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1028159589 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_308267,RMVar_hsa_circ_305538,RMVar_hsa_circ_108317,RMVar_hsa_circ_144203,RMVar_hsa_circ_311083,RMVar_hsa_circ_144202 22394 RMVar_ID_22394 Human_SNP_ID_437563134 A-to-I Human chr10 + 72850047 72850047 72850047 GTAATTCTCTTGCCTCAGGTGCCTGAATAGCTAGGATTACAGGTGTCTGCCACCACACCCAGCTA GTAATTCTCTTGCCTCAGGTGCCTGAATAGCTGGGATTACAGGTGTCTGCCACCACACCCAGCTA A G MCU Ensembl:ENSG00000156026 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1458416615 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108317,RMVar_hsa_circ_144202,RMVar_hsa_circ_285484,RMVar_hsa_circ_325951,RMVar_hsa_circ_144210 22395 RMVar_ID_22395 Human_SNP_ID_437600849 A-to-I Human chr10 - 73010714 73010714 73010714 CAGGTGCATGTCACCATGCCCAGCTAATGTTTAAATTTTTTGTAGAGACAGTGTCTCCCTGTATT CAGGTGCATGTCACCATGCCCAGCTAATGTTTGAATTTTTTGTAGAGACAGTGTCTCCCTGTATT T C P4HA1 Ensembl:ENSG00000122884 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1294545439 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61722,RMVar_hsa_circ_368080,RMVar_hsa_circ_144224 22396 RMVar_ID_22396 Human_SNP_ID_437600855 A-to-I Human chr10 - 73010747 73010747 73010747 TTCAAGCCTCAGCCTCCCAAATAGTGGGGACTACAGGTGCATGTCACCATGCCCAGCTAATGTTT TTCAAGCCTCAGCCTCCCAAATAGTGGGGACTGCAGGTGCATGTCACCATGCCCAGCTAATGTTT T C P4HA1 Ensembl:ENSG00000122884 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1278718314 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61722,RMVar_hsa_circ_368080,RMVar_hsa_circ_144224 22397 RMVar_ID_22397 Human_SNP_ID_437606823 A-to-I Human chr10 - 73035412 73035412 73035412 CTCAAGCAATCCTCCTGCCTCAGCCTCTAAGTAGCTGAAACTATAAACCTGTGCCACCACACCTT CTCAAGCAATCCTCCTGCCTCAGCCTCTAAGTCGCTGAAACTATAAACCTGTGCCACCACACCTT T G P4HA1 Ensembl:ENSG00000122884 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs893359398 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_144227,RMVar_hsa_circ_144225,RMVar_hsa_circ_61722,RMVar_hsa_circ_360009,RMVar_hsa_circ_144224,RMVar_hsa_circ_358787,RMVar_hsa_circ_72868,RMVar_hsa_circ_29150,RMVar_hsa_circ_313690,RMVar_hsa_circ_350480,RMVar_hsa_circ_355575,RMVar_hsa_circ_355746,RMVar_hsa_circ_327449,RMVar_hsa_circ_7732,RMVar_hsa_circ_314169,RMVar_hsa_circ_144226,RMVar_hsa_circ_59775,RMVar_hsa_circ_82292,RMVar_hsa_circ_144229,RMVar_hsa_circ_94809,RMVar_hsa_circ_277807,RMVar_hsa_circ_310326,RMVar_hsa_circ_348060,RMVar_hsa_circ_302346,RMVar_hsa_circ_273347,RMVar_hsa_circ_144231,RMVar_hsa_circ_144232,RMVar_hsa_circ_144230,RMVar_hsa_circ_144228 22398 RMVar_ID_22398 Human_SNP_ID_437607669 A-to-I Human chr10 - 73038133 73038133 73038133 CTCCCACCTCAGCCTCCTGAGTAACTGGGGCTACGGGTGCACACCACCATGCCCAGCTAAGTTTT CTCCCACCTCAGCCTCCTGAGTAACTGGGGCTGCGGGTGCACACCACCATGCCCAGCTAAGTTTT T C P4HA1 Ensembl:ENSG00000122884 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1350792673 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_144227,RMVar_hsa_circ_144225,RMVar_hsa_circ_61722,RMVar_hsa_circ_360009,RMVar_hsa_circ_144224,RMVar_hsa_circ_358787,RMVar_hsa_circ_72868,RMVar_hsa_circ_29150,RMVar_hsa_circ_313690,RMVar_hsa_circ_350480,RMVar_hsa_circ_355575,RMVar_hsa_circ_355746,RMVar_hsa_circ_327449,RMVar_hsa_circ_7732,RMVar_hsa_circ_314169,RMVar_hsa_circ_144226,RMVar_hsa_circ_59775,RMVar_hsa_circ_82292,RMVar_hsa_circ_144229,RMVar_hsa_circ_94809,RMVar_hsa_circ_277807,RMVar_hsa_circ_310326,RMVar_hsa_circ_348060,RMVar_hsa_circ_302346,RMVar_hsa_circ_273347,RMVar_hsa_circ_144231,RMVar_hsa_circ_144232,RMVar_hsa_circ_144230,RMVar_hsa_circ_144228 22399 RMVar_ID_22399 Human_SNP_ID_437607676 A-to-I Human chr10 - 73038168 73038168 73038168 TCACTACAGCCTCCACCTCCCAGGCTCAAGCAATCCTCCCACCTCAGCCTCCTGAGTAACTGGGG TCACTACAGCCTCCACCTCCCAGGCTCAAGCAGTCCTCCCACCTCAGCCTCCTGAGTAACTGGGG T C P4HA1 Ensembl:ENSG00000122884 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs780492089 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_144227,RMVar_hsa_circ_144225,RMVar_hsa_circ_61722,RMVar_hsa_circ_360009,RMVar_hsa_circ_144224,RMVar_hsa_circ_358787,RMVar_hsa_circ_72868,RMVar_hsa_circ_29150,RMVar_hsa_circ_313690,RMVar_hsa_circ_350480,RMVar_hsa_circ_355575,RMVar_hsa_circ_355746,RMVar_hsa_circ_327449,RMVar_hsa_circ_7732,RMVar_hsa_circ_314169,RMVar_hsa_circ_144226,RMVar_hsa_circ_59775,RMVar_hsa_circ_82292,RMVar_hsa_circ_144229,RMVar_hsa_circ_94809,RMVar_hsa_circ_277807,RMVar_hsa_circ_310326,RMVar_hsa_circ_348060,RMVar_hsa_circ_302346,RMVar_hsa_circ_273347,RMVar_hsa_circ_144231,RMVar_hsa_circ_144232,RMVar_hsa_circ_144230,RMVar_hsa_circ_144228 22400 RMVar_ID_22400 Human_SNP_ID_437608030 A-to-I Human chr10 - 73039438 73039438 73039438 GCCGGGCATGGTGGCGGGTGCCTGTGGTCCCAACTACTGGGGAGGCTGAGGCAGGAGAACGGCAG GCCGGGCATGGTGGCGGGTGCCTGTGGTCCCAGCTACTGGGGAGGCTGAGGCAGGAGAACGGCAG T C P4HA1 Ensembl:ENSG00000122884 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs192625258 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_144227,RMVar_hsa_circ_144225,RMVar_hsa_circ_61722,RMVar_hsa_circ_360009,RMVar_hsa_circ_144224,RMVar_hsa_circ_358787,RMVar_hsa_circ_72868,RMVar_hsa_circ_29150,RMVar_hsa_circ_313690,RMVar_hsa_circ_350480,RMVar_hsa_circ_355575,RMVar_hsa_circ_355746,RMVar_hsa_circ_327449,RMVar_hsa_circ_7732,RMVar_hsa_circ_314169,RMVar_hsa_circ_144226,RMVar_hsa_circ_59775,RMVar_hsa_circ_82292,RMVar_hsa_circ_144229,RMVar_hsa_circ_94809,RMVar_hsa_circ_277807,RMVar_hsa_circ_310326,RMVar_hsa_circ_348060,RMVar_hsa_circ_302346,RMVar_hsa_circ_273347,RMVar_hsa_circ_144231,RMVar_hsa_circ_144232,RMVar_hsa_circ_144230,RMVar_hsa_circ_144228 22401 RMVar_ID_22401 Human_SNP_ID_437608187 A-to-I Human chr10 - 73039964 73039964 73039964 CCAGCTACCCAGGAGGCTTAGGTGGGTAGATCACTTGAGCCTGGGAAGCAGAGATTGCAGTGAGC CCAGCTACCCAGGAGGCTTAGGTGGGTAGATCCCTTGAGCCTGGGAAGCAGAGATTGCAGTGAGC T G P4HA1 Ensembl:ENSG00000122884 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1005390945 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_144227,RMVar_hsa_circ_144225,RMVar_hsa_circ_61722,RMVar_hsa_circ_360009,RMVar_hsa_circ_144224,RMVar_hsa_circ_358787,RMVar_hsa_circ_72868,RMVar_hsa_circ_29150,RMVar_hsa_circ_313690,RMVar_hsa_circ_350480,RMVar_hsa_circ_355575,RMVar_hsa_circ_355746,RMVar_hsa_circ_327449,RMVar_hsa_circ_7732,RMVar_hsa_circ_314169,RMVar_hsa_circ_144226,RMVar_hsa_circ_59775,RMVar_hsa_circ_82292,RMVar_hsa_circ_144229,RMVar_hsa_circ_94809,RMVar_hsa_circ_277807,RMVar_hsa_circ_310326,RMVar_hsa_circ_348060,RMVar_hsa_circ_302346,RMVar_hsa_circ_273347,RMVar_hsa_circ_144231,RMVar_hsa_circ_144232,RMVar_hsa_circ_144230,RMVar_hsa_circ_144228 22402 RMVar_ID_22402 Human_SNP_ID_437610103 A-to-I Human chr10 - 73047989 73047989 73047989 GGAGTGTAGTGGCATGATCATGGCTCACTGCAACCTCTACCTCCTGGGCTTAAGCAGTCCTCCCA GGAGTGTAGTGGCATGATCATGGCTCACTGCAGCCTCTACCTCCTGGGCTTAAGCAGTCCTCCCA T C P4HA1 Ensembl:ENSG00000122884 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1259746729 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_532,RMVar_hsa_circ_360009,RMVar_hsa_circ_144224,RMVar_hsa_circ_72868,RMVar_hsa_circ_29150,RMVar_hsa_circ_350480,RMVar_hsa_circ_355575,RMVar_hsa_circ_327449,RMVar_hsa_circ_7732,RMVar_hsa_circ_314169,RMVar_hsa_circ_144226,RMVar_hsa_circ_3527,RMVar_hsa_circ_144229,RMVar_hsa_circ_94809,RMVar_hsa_circ_277807,RMVar_hsa_circ_310326,RMVar_hsa_circ_348060,RMVar_hsa_circ_302346,RMVar_hsa_circ_144231,RMVar_hsa_circ_144232,RMVar_hsa_circ_144230,RMVar_hsa_circ_356273,RMVar_hsa_circ_282318,RMVar_hsa_circ_94411,RMVar_hsa_circ_350929,RMVar_hsa_circ_360546,RMVar_hsa_circ_373696,RMVar_hsa_circ_144236,RMVar_hsa_circ_144237,RMVar_hsa_circ_144235,RMVar_hsa_circ_355843,RMVar_hsa_circ_71154 22403 RMVar_ID_22403 Human_SNP_ID_437614084 A-to-I Human chr10 - 73064292 73064292 73064292 TTTTGTATTTTTTGTAGAGACAGGGTTTTGCCATGTTATCCAGGCTGGTTTCGAACTCCTGAGCT TTTTGTATTTTTTGTAGAGACAGGGTTTTGCCTTGTTATCCAGGCTGGTTTCGAACTCCTGAGCT T A P4HA1 Ensembl:ENSG00000122884 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1190628315 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11421173 RMVar_hsa_circ_144224,RMVar_hsa_circ_72868,RMVar_hsa_circ_29150,RMVar_hsa_circ_350480,RMVar_hsa_circ_314169,RMVar_hsa_circ_3527,RMVar_hsa_circ_94809,RMVar_hsa_circ_310326,RMVar_hsa_circ_302346,RMVar_hsa_circ_144231,RMVar_hsa_circ_144232,RMVar_hsa_circ_144230,RMVar_hsa_circ_282318,RMVar_hsa_circ_94411,RMVar_hsa_circ_350929,RMVar_hsa_circ_373696,RMVar_hsa_circ_144236,RMVar_hsa_circ_144237,RMVar_hsa_circ_144235,RMVar_hsa_circ_355843,RMVar_hsa_circ_71154,RMVar_hsa_circ_348793,RMVar_hsa_circ_314896 22404 RMVar_ID_22404 Human_SNP_ID_437614085 A-to-I Human chr10 - 73064292 73064292 73064292 TTTTGTATTTTTTGTAGAGACAGGGTTTTGCCATGTTATCCAGGCTGGTTTCGAACTCCTGAGCT TTTTGTATTTTTTGTAGAGACAGGGTTTTGCCGTGTTATCCAGGCTGGTTTCGAACTCCTGAGCT T C P4HA1 Ensembl:ENSG00000122884 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1190628315 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11421173 RMVar_hsa_circ_144224,RMVar_hsa_circ_72868,RMVar_hsa_circ_29150,RMVar_hsa_circ_350480,RMVar_hsa_circ_314169,RMVar_hsa_circ_3527,RMVar_hsa_circ_94809,RMVar_hsa_circ_310326,RMVar_hsa_circ_302346,RMVar_hsa_circ_144231,RMVar_hsa_circ_144232,RMVar_hsa_circ_144230,RMVar_hsa_circ_282318,RMVar_hsa_circ_94411,RMVar_hsa_circ_350929,RMVar_hsa_circ_373696,RMVar_hsa_circ_144236,RMVar_hsa_circ_144237,RMVar_hsa_circ_144235,RMVar_hsa_circ_355843,RMVar_hsa_circ_71154,RMVar_hsa_circ_348793,RMVar_hsa_circ_314896 22405 RMVar_ID_22405 Human_SNP_ID_437615426 A-to-I Human chr10 - 73070060 73070060 73070060 CATGCCTGTAATCCCAGCACTTTGGGAGACCAAGGCAGGTGGATCGTTTGAGACCAGGAGTTGGA CATGCCTGTAATCCCAGCACTTTGGGAGACCATGGCAGGTGGATCGTTTGAGACCAGGAGTTGGA T A P4HA1 Ensembl:ENSG00000122884 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1187008920 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_144224,RMVar_hsa_circ_29150,RMVar_hsa_circ_3527,RMVar_hsa_circ_94809,RMVar_hsa_circ_310326,RMVar_hsa_circ_144231,RMVar_hsa_circ_144232,RMVar_hsa_circ_94411,RMVar_hsa_circ_373696,RMVar_hsa_circ_144236,RMVar_hsa_circ_144237,RMVar_hsa_circ_355843,RMVar_hsa_circ_144239,RMVar_hsa_circ_316815 22406 RMVar_ID_22406 Human_SNP_ID_437617802 A-to-I Human chr10 - 73079550 73079550 73079550 TTTGGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGGTTTCGAACTCCTCACCTCAGGTGATC TTTGGTAGAGACGGGGTTTCACCATGTTGGCCTGGCTGGTTTCGAACTCCTCACCTCAGGTGATC T A P4HA1 Ensembl:ENSG00000122884 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569999988 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94411,RMVar_hsa_circ_144237 22407 RMVar_ID_22407 Human_SNP_ID_437620172 A-to-I Human chr10 - 73089975 73089975 73089975 TTAAAAAGCCAGGTGTGGTGTTGTGTGCCTGCAGTCCCCGCTACTTGGGAGACTGAGGTGGGAGA TTAAAAAGCCAGGTGTGGTGTTGTGTGCCTGCCGTCCCCGCTACTTGGGAGACTGAGGTGGGAGA T G P4HA1 Ensembl:ENSG00000122884 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs545663477 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94411,RMVar_hsa_circ_144237 22408 RMVar_ID_22408 Human_SNP_ID_437620217 A-to-I Human chr10 - 73090100 73090100 73090100 GCCAGGCGCAGTGGCTCACACCTGTAATCCCAACACTCTGGGGGGCCGAGGCAGGAGGACTGCTT GCCAGGCGCAGTGGCTCACACCTGTAATCCCAGCACTCTGGGGGGCCGAGGCAGGAGGACTGCTT T C P4HA1 Ensembl:ENSG00000122884 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1027044230 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94411,RMVar_hsa_circ_144237 22409 RMVar_ID_22409 Human_SNP_ID_437620286 A-to-I Human chr10 - 73090401 73090401 73090401 GGTCAGGCACAGTGGCTTAGGCCTGTAATCCCAACCCTTTGGGTGGCCGAGGCAGGAGGACTGCT GGTCAGGCACAGTGGCTTAGGCCTGTAATCCCGACCCTTTGGGTGGCCGAGGCAGGAGGACTGCT T C P4HA1 Ensembl:ENSG00000122884 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1383090680 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94411,RMVar_hsa_circ_144237 22410 RMVar_ID_22410 Human_SNP_ID_437620287 A-to-I Human chr10 - 73090406 73090405 73090406 CTCAAGGTCAGGCACAGTGGCTTAGGCCTGTAATCCCAACCCTTTGGGTGGCCGAGGCAGGAGGA CTCAAGGTCAGGCACAGTGGCTTAGGCCTGTA_TCCCAACCCTTTGGGTGGCCGAGGCAGGAGGA AT A P4HA1 Ensembl:ENSG00000122884 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1180138670 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_94411,RMVar_hsa_circ_144237 22411 RMVar_ID_22411 Human_SNP_ID_437620994 A-to-I Human chr10 - 73093034 73093034 73093034 CTCACTGCAGCCTTGAACTCCTGGGCTCAAGCAATCCTTCTGCCTCAGCCTCCGGGTGTAGCTCG CTCACTGCAGCCTTGAACTCCTGGGCTCAAGCCATCCTTCTGCCTCAGCCTCCGGGTGTAGCTCG T G P4HA1 Ensembl:ENSG00000122884 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1050854384 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94411,RMVar_hsa_circ_144237 22412 RMVar_ID_22412 Human_SNP_ID_437621166 A-to-I Human chr10 - 73093721 73093721 73093721 CTCCTGCCTAAGCCTCCCGAGTAGCTGGGACTACAGCCGCCCACCATCACGCCCAGCTAATTTTT CTCCTGCCTAAGCCTCCCGAGTAGCTGGGACTGCAGCCGCCCACCATCACGCCCAGCTAATTTTT T C P4HA1 Ensembl:ENSG00000122884 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs553439310 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94411,RMVar_hsa_circ_144237 22413 RMVar_ID_22413 Human_SNP_ID_437626989 A-to-I Human chr10 - 73116723 73116721 73116723 AATTTTTTTTCTTTGAGACAGGGTCTCACTCTATCATGCAGGCTAGAGTGCAATGACACGATCTC AATTTTTTTTCTTTGAGACAGGGTCTCACTCT__CATGCAGGCTAGAGTGCAATGACACGATCTC GAT G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1324131080 Functional Loss DEL dbSNP153 33..34 33 - - - 22414 RMVar_ID_22414 Human_SNP_ID_437626991 A-to-I Human chr10 - 73116723 73116723 73116723 AATTTTTTTTCTTTGAGACAGGGTCTCACTCTATCATGCAGGCTAGAGTGCAATGACACGATCTC AATTTTTTTTCTTTGAGACAGGGTCTCACTCTGTCATGCAGGCTAGAGTGCAATGACACGATCTC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027783748 Functional Loss SNV dbSNP153 33..33 33 - - - 22415 RMVar_ID_22415 Human_SNP_ID_437627182 A-to-I Human chr10 - 73117474 73117474 73117474 TGGCTCACTGTAACCTCTGCCTCCCGGGTCCAAGTGATTCTCTTGCCTCAGCCTCCCAAGTAGCT TGGCTCACTGTAACCTCTGCCTCCCGGGTCCAGGTGATTCTCTTGCCTCAGCCTCCCAAGTAGCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1016393102 Functional Loss SNV dbSNP153 33..33 33 - - - 22416 RMVar_ID_22416 Human_SNP_ID_437629470 A-to-I Human chr10 - 73127251 73127251 73127251 CCTCAGCCTCCCAAATAGCTGGGACTACAGGCACCTGCCACCATGCCGAGCCAATTTTTGTATTT CCTCAGCCTCCCAAATAGCTGGGACTACAGGCCCCTGCCACCATGCCGAGCCAATTTTTGTATTT T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053267861 Functional Loss SNV dbSNP153 33..33 33 - - - 22417 RMVar_ID_22417 Human_SNP_ID_437632875 A-to-I Human chr10 - 73142046 73142046 73142046 TACTTGCTGAGATAGGAAGATTGCTTGATCCCAAGAGTCAAGGCTGCAGTGAGCTGTGATCATGC TACTTGCTGAGATAGGAAGATTGCTTGATCCCGAGAGTCAAGGCTGCAGTGAGCTGTGATCATGC T C ECD Ensembl:ENSG00000122882 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1564660869 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2347,RMVar_hsa_circ_144244,RMVar_hsa_circ_90671,RMVar_hsa_circ_95162,RMVar_hsa_circ_144245,RMVar_hsa_circ_144246,RMVar_hsa_circ_144247,RMVar_hsa_circ_45340,RMVar_hsa_circ_16864,RMVar_hsa_circ_371099,RMVar_hsa_circ_53131,RMVar_hsa_circ_144250,RMVar_hsa_circ_12245 22418 RMVar_ID_22418 Human_SNP_ID_437633174 A-to-I Human chr10 - 73143306 73143306 73143306 AAATTAGCTGGGCGTGTTGGCACGCCCCTGTAATCCCAGCTGCTCGGGAGGCTGAGGCAGGAGAA AAATTAGCTGGGCGTGTTGGCACGCCCCTGTAGTCCCAGCTGCTCGGGAGGCTGAGGCAGGAGAA T C ECD Ensembl:ENSG00000122882 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1160347581 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2347,RMVar_hsa_circ_144244,RMVar_hsa_circ_90671,RMVar_hsa_circ_95162,RMVar_hsa_circ_144245,RMVar_hsa_circ_144246,RMVar_hsa_circ_144247,RMVar_hsa_circ_45340,RMVar_hsa_circ_16864,RMVar_hsa_circ_371099,RMVar_hsa_circ_53131,RMVar_hsa_circ_144250,RMVar_hsa_circ_12245 22419 RMVar_ID_22419 Human_SNP_ID_437633589 A-to-I Human chr10 - 73145107 73145107 73145107 CACCCACCTTGGCCTCCCAAAGTGCTGAGATTACAGGCGTGAGCCAATGCACCCAGCCATTAATT CACCCACCTTGGCCTCCCAAAGTGCTGAGATTGCAGGCGTGAGCCAATGCACCCAGCCATTAATT T C ECD Ensembl:ENSG00000122882 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs964150985 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2347,RMVar_hsa_circ_144244,RMVar_hsa_circ_90671,RMVar_hsa_circ_95162,RMVar_hsa_circ_144245,RMVar_hsa_circ_144246,RMVar_hsa_circ_144247,RMVar_hsa_circ_45340,RMVar_hsa_circ_16864,RMVar_hsa_circ_371099,RMVar_hsa_circ_53131,RMVar_hsa_circ_144250,RMVar_hsa_circ_12245 22420 RMVar_ID_22420 Human_SNP_ID_437636561 A-to-I Human chr10 - 73157181 73157181 73157181 GCTGGGCATGATGGCGGGCACTTGTAATCCCAACTACTCAGGAGGCTGAGGCAGGATAATTGCCT GCTGGGCATGATGGCGGGCACTTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGATAATTGCCT T C ECD Ensembl:ENSG00000122882 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1449751921 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32760,RMVar_hsa_circ_2347,RMVar_hsa_circ_90671,RMVar_hsa_circ_144245,RMVar_hsa_circ_144247,RMVar_hsa_circ_12245,RMVar_hsa_circ_311340,RMVar_hsa_circ_144251,RMVar_hsa_circ_299308,RMVar_hsa_circ_278929,RMVar_hsa_circ_144254,RMVar_hsa_circ_144256,RMVar_hsa_circ_292546,RMVar_hsa_circ_144258,RMVar_hsa_circ_307507 22421 RMVar_ID_22421 Human_SNP_ID_437637245 A-to-I Human chr10 - 73160055 73160055 73160055 CTCTGGAGCTCCTGACCTCAGGTGATCCACCCACCTTGGCCTCCCAAAGTGCTGGGAATACAGGC CTCTGGAGCTCCTGACCTCAGGTGATCCACCCGCCTTGGCCTCCCAAAGTGCTGGGAATACAGGC T C ECD Ensembl:ENSG00000122882 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs981814715 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24831628 RMVar_hsa_circ_32760,RMVar_hsa_circ_2347,RMVar_hsa_circ_90671,RMVar_hsa_circ_144245,RMVar_hsa_circ_144247,RMVar_hsa_circ_12245,RMVar_hsa_circ_311340,RMVar_hsa_circ_144251,RMVar_hsa_circ_299308,RMVar_hsa_circ_278929,RMVar_hsa_circ_144254,RMVar_hsa_circ_144256,RMVar_hsa_circ_292546,RMVar_hsa_circ_144258,RMVar_hsa_circ_307507 22422 RMVar_ID_22422 Human_SNP_ID_437650569 A-to-I Human chr10 + 73220947 73220947 73220947 GTACACCATGCAATGGAATATTATTCAGCCACAAAGAGGAATTAAGTACTGATACATGTTACAAC GTACACCATGCAATGGAATATTATTCAGCCACGAAGAGGAATTAAGTACTGATACATGTTACAAC A G FAM149B1 Ensembl:ENSG00000138286 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs570329462 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86639,RMVar_hsa_circ_304562,RMVar_hsa_circ_51977,RMVar_hsa_circ_144260,RMVar_hsa_circ_364909,RMVar_hsa_circ_144270,RMVar_hsa_circ_376253,RMVar_hsa_circ_335207,RMVar_hsa_circ_144271 22423 RMVar_ID_22423 Human_SNP_ID_437652265 A-to-I Human chr10 - 73228730 73228730 73228730 TCAGCCGAGTGGTGGTGCACATCTGTAATCCCAGGTACTCAGGGGGCTGAGGCACAAGAACTGGT TCAGCCGAGTGGTGGTGCACATCTGTAATCCCCGGTACTCAGGGGGCTGAGGCACAAGAACTGGT T G DNAJC9 Ensembl:ENSG00000213551 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1421278820 Functional Loss SNV dbSNP153 33..33 33 - - - 22424 RMVar_ID_22424 Human_SNP_ID_437654307 A-to-I Human chr10 - 73236913 73236910 73236913 ACCTCGGAGTTTGAGACCAGTCTGGCCAACATAGTGACACCCTATCTCTACAAAATAAAAAAATT ACCTCGGAGTTTGAGACCAGTCTGGCCAACAT___GACACCCTATCTCTACAAAATAAAAAAATT CACT C DNAJC9 Ensembl:ENSG00000213551 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1208335737 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_11422466 22425 RMVar_ID_22425 Human_SNP_ID_437654477 A-to-I Human chr10 - 73237668 73237668 73237668 CCTGTAATCCCAGCACTTTGGGAGGCCAAGGTAGGTGGATCACTTGGGGTCAGAAGTTCAAGACC CCTGTAATCCCAGCACTTTGGGAGGCCAAGGTTGGTGGATCACTTGGGGTCAGAAGTTCAAGACC T A DNAJC9 Ensembl:ENSG00000213551 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1307537566 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17558831 22426 RMVar_ID_22426 Human_SNP_ID_437654636 A-to-I Human chr10 - 73238308 73238308 73238308 TCTTCTCGCTCTGTCGCCCAGGTTGGAGTGCAATGGCACGATCTCGGCTCACTGCAACCTCTGCC TCTTCTCGCTCTGTCGCCCAGGTTGGAGTGCAGTGGCACGATCTCGGCTCACTGCAACCTCTGCC T C DNAJC9 Ensembl:ENSG00000213551 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs949625421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22788661 22427 RMVar_ID_22427 Human_SNP_ID_437657716 A-to-I Human chr10 - 73248973 73248973 73248973 CCGATGCTGCAGTGAACTGTGATTGTTCCACTACAGTCCAGCCTGGGTGACAGAGAAAAGAAAAA CCGATGCTGCAGTGAACTGTGATTGTTCCACTGCAGTCCAGCCTGGGTGACAGAGAAAAGAAAAA T C MRPS16 Ensembl:ENSG00000182180 Protein coding exon GSE38233;GSE100210;GSE112787 cultured B-cells;HepG2 cell line;293 Flip-In T-REx cells,empty vector - 24183664,29129909,29967493 RNA-Seq:(High) rs1133556 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_382131,Human_RBP_ID_1449806,Human_RBP_ID_3356805,Human_RBP_ID_4127005,Human_RBP_ID_5998321,Human_RBP_ID_8338775,Human_RBP_ID_22155502,Human_RBP_ID_23468496,Human_RBP_ID_24831877,Human_RBP_ID_26398405 Human_miRNA_ID_291237,Human_miRNA_ID_1980706,Human_miRNA_ID_1982430,Human_miRNA_ID_2541881,Human_miRNA_ID_2543755,Human_miRNA_ID_2545605,Human_miRNA_ID_2547460,Human_miRNA_ID_2549324,Human_miRNA_ID_2551193,Human_miRNA_ID_2556600,Human_miRNA_ID_2558482,Human_miRNA_ID_2588901 RMVar_hsa_circ_82619,RMVar_hsa_circ_127977,RMVar_hsa_circ_144275,RMVar_hsa_circ_144276 22428 RMVar_ID_22428 Human_SNP_ID_437657737 A-to-I Human chr10 - 73249034 73249034 73249034 CTCACCCATAGTTCCAGCTACTCGGGAAGCTGAGGCAGTAAGATCACTTGAGCCCAGGAGGCCGA CTCACCCATAGTTCCAGCTACTCGGGAAGCTGGGGCAGTAAGATCACTTGAGCCCAGGAGGCCGA T C MRPS16 Ensembl:ENSG00000182180 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-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 22429 RMVar_ID_22429 Human_SNP_ID_437657740 A-to-I Human chr10 - 73249047 73249047 73249047 GGCTGTGGTGTTGCTCACCCATAGTTCCAGCTACTCGGGAAGCTGAGGCAGTAAGATCACTTGAG GGCTGTGGTGTTGCTCACCCATAGTTCCAGCTGCTCGGGAAGCTGAGGCAGTAAGATCACTTGAG T C MRPS16 Ensembl:ENSG00000182180 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1133544 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_382133,Human_RBP_ID_5998325,Human_RBP_ID_11422913,Human_RBP_ID_17782268,Human_RBP_ID_26398406,Human_RBP_ID_26881968 RMVar_hsa_circ_82619,RMVar_hsa_circ_127977,RMVar_hsa_circ_144275,RMVar_hsa_circ_144276 22430 RMVar_ID_22430 Human_SNP_ID_437657742 A-to-I Human chr10 - 73249057 73249057 73249057 AAAATTAGCTGGCTGTGGTGTTGCTCACCCATAGTTCCAGCTACTCGGGAAGCTGAGGCAGTAAG AAAATTAGCTGGCTGTGGTGTTGCTCACCCATGGTTCCAGCTACTCGGGAAGCTGAGGCAGTAAG T C MRPS16 Ensembl:ENSG00000182180 Protein coding exon GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1071674 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_382133,Human_RBP_ID_5998325,Human_RBP_ID_11422913,Human_RBP_ID_17782269,Human_RBP_ID_24860696,Human_RBP_ID_26398407 RMVar_hsa_circ_82619,RMVar_hsa_circ_127977,RMVar_hsa_circ_144275,RMVar_hsa_circ_144276 22431 RMVar_ID_22431 Human_SNP_ID_437657743 A-to-I Human chr10 - 73249059 73249059 73249059 AAAAAATTAGCTGGCTGTGGTGTTGCTCACCCATAGTTCCAGCTACTCGGGAAGCTGAGGCAGTA AAAAAATTAGCTGGCTGTGGTGTTGCTCACCCGTAGTTCCAGCTACTCGGGAAGCTGAGGCAGTA T C MRPS16 Ensembl:ENSG00000182180 Protein coding exon GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1133542 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_382133,Human_RBP_ID_5998325,Human_RBP_ID_11422913,Human_RBP_ID_17782269,Human_RBP_ID_26398407 RMVar_hsa_circ_82619,RMVar_hsa_circ_127977,RMVar_hsa_circ_144275,RMVar_hsa_circ_144276 22432 RMVar_ID_22432 Human_SNP_ID_437657747 A-to-I Human chr10 - 73249083 73249083 73249083 AAGACCCCGTCTCTACAAAAACTTAAAAAATTAGCTGGCTGTGGTGTTGCTCACCCATAGTTCCA AAGACCCCGTCTCTACAAAAACTTAAAAAATTGGCTGGCTGTGGTGTTGCTCACCCATAGTTCCA T C MRPS16 Ensembl:ENSG00000182180 Protein coding exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1133541 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5998326,Human_RBP_ID_8762992,Human_RBP_ID_9606916,Human_RBP_ID_11422914,Human_RBP_ID_17782269,Human_RBP_ID_22887772,Human_RBP_ID_24860697,Human_RBP_ID_26398407,Human_RBP_ID_27408313 RMVar_hsa_circ_82619,RMVar_hsa_circ_127977,RMVar_hsa_circ_144275,RMVar_hsa_circ_144276 22433 RMVar_ID_22433 Human_SNP_ID_437657749 A-to-I Human chr10 - 73249086 73249086 73249086 AGCAAGACCCCGTCTCTACAAAAACTTAAAAAATTAGCTGGCTGTGGTGTTGCTCACCCATAGTT AGCAAGACCCCGTCTCTACAAAAACTTAAAAAGTTAGCTGGCTGTGGTGTTGCTCACCCATAGTT T C MRPS16 Ensembl:ENSG00000182180 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1133539 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5998326,Human_RBP_ID_8762992,Human_RBP_ID_9606916,Human_RBP_ID_11422914,Human_RBP_ID_17782270,Human_RBP_ID_22887772,Human_RBP_ID_24831878,Human_RBP_ID_26398407,Human_RBP_ID_27408313 RMVar_hsa_circ_82619,RMVar_hsa_circ_127977,RMVar_hsa_circ_144275,RMVar_hsa_circ_144276 22434 RMVar_ID_22434 Human_SNP_ID_437657751 A-to-I Human chr10 - 73249097 73249097 73249097 CTGTGCAACACAGCAAGACCCCGTCTCTACAAAAACTTAAAAAATTAGCTGGCTGTGGTGTTGCT CTGTGCAACACAGCAAGACCCCGTCTCTACAAGAACTTAAAAAATTAGCTGGCTGTGGTGTTGCT T C MRPS16 Ensembl:ENSG00000182180 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-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 22435 RMVar_ID_22435 Human_SNP_ID_437657761 A-to-I Human chr10 - 73249118 73249118 73249118 AAGCCAGAGTTTGAGACCAGCCTGTGCAACACAGCAAGACCCCGTCTCTACAAAAACTTAAAAAA AAGCCAGAGTTTGAGACCAGCCTGTGCAACACGGCAAGACCCCGTCTCTACAAAAACTTAAAAAA T C MRPS16 Ensembl:ENSG00000182180 Protein coding exon GSE38233;GSE100210;GSE112787 cultured B-cells;HepG2 cell line;293 Flip-In T-REx cells,empty vector - 24183664,29129909,29967493 RNA-Seq:(High) rs1133529 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5998328,Human_RBP_ID_11422919,Human_RBP_ID_26396661 RMVar_hsa_circ_82619,RMVar_hsa_circ_127977,RMVar_hsa_circ_144275,RMVar_hsa_circ_144276 22436 RMVar_ID_22436 Human_SNP_ID_437657774 A-to-I Human chr10 - 73249197 73249197 73249197 AATATAAAGATACCATTGGGGCAGTGGCTCACACCTGTAATCTCAGCACTTTGGGAGGCTGAGGT AATATAAAGATACCATTGGGGCAGTGGCTCACGCCTGTAATCTCAGCACTTTGGGAGGCTGAGGT T C MRPS16 Ensembl:ENSG00000182180 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-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 22437 RMVar_ID_22437 Human_SNP_ID_437657776 A-to-I Human chr10 - 73249207 73249207 73249207 AAGGAAAAATAATATAAAGATACCATTGGGGCAGTGGCTCACACCTGTAATCTCAGCACTTTGGG AAGGAAAAATAATATAAAGATACCATTGGGGCGGTGGCTCACACCTGTAATCTCAGCACTTTGGG T C MRPS16 Ensembl:ENSG00000182180 Protein coding exon GSE38233;GSE100210;GSE107867;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;ASD brains,cerebellum;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,30559470,32596459,32596459 RNA-Seq:(High) rs563025614 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8172668,Human_RBP_ID_26398410 RMVar_hsa_circ_82619,RMVar_hsa_circ_127977,RMVar_hsa_circ_144275,RMVar_hsa_circ_144276 22438 RMVar_ID_22438 Human_SNP_ID_437657911 A-to-I Human chr10 - 73249834 73249834 73249834 TGACCTTGTGATCTGCCCACCTCGGCCTCCCAAAGTGCTAGGATTACTGGCGTGAGCCACCACTC TGACCTTGTGATCTGCCCACCTCGGCCTCCCAGAGTGCTAGGATTACTGGCGTGAGCCACCACTC T C MRPS16 Ensembl:ENSG00000182180 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs761233663 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11422945,Human_RBP_ID_24401974,Human_RBP_ID_26396688 RMVar_hsa_circ_82619,RMVar_hsa_circ_127977,RMVar_hsa_circ_144275,RMVar_hsa_circ_144276 22439 RMVar_ID_22439 Human_SNP_ID_437657912 A-to-I Human chr10 - 73249835 73249835 73249835 CTGACCTTGTGATCTGCCCACCTCGGCCTCCCAAAGTGCTAGGATTACTGGCGTGAGCCACCACT CTGACCTTGTGATCTGCCCACCTCGGCCTCCCGAAGTGCTAGGATTACTGGCGTGAGCCACCACT T C MRPS16 Ensembl:ENSG00000182180 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs550900634 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4127036,Human_RBP_ID_11422945,Human_RBP_ID_24401974,Human_RBP_ID_26396688 RMVar_hsa_circ_82619,RMVar_hsa_circ_127977,RMVar_hsa_circ_144275,RMVar_hsa_circ_144276 22440 RMVar_ID_22440 Human_SNP_ID_437657930 A-to-I Human chr10 - 73250023 73249890 73250023 TTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTATCCAGGATGGTTTTGATCTCCTGACCT TTTTGTATTTTTAGTAGAGATGGGGTTTCAC__________________________________ CGGTGAAACCCCATCTCTACTAAAAATACAAAAATTTGCCCGGGCGGTGGCTCACGCCTATAATCCCAGCACTTTTGGGAGGCCAAGGCGGGCGGATCACGAGGTCAGGAGATCAAAACCATCCTGGATAACAT C MRPS16 Ensembl:ENSG00000182180 Protein coding exon GSE38233;GSE107867;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;ASD brains,frontal_cortex;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,30559470,32596459 RNA-Seq:(High) rs1564725816 Functional Loss DEL dbSNP153 32..65 33 - - - Human_RBP_ID_11422954 RMVar_hsa_circ_82619,RMVar_hsa_circ_127977,RMVar_hsa_circ_144275,RMVar_hsa_circ_144276 22441 RMVar_ID_22441 Human_SNP_ID_437657956 A-to-I Human chr10 - 73249962 73249961 73249962 ACCTCGTGATCCGCCCGCCTTGGCCTCCCAAAAGTGCTGGGATTATAGGCGTGAGCCACCGCCCG ACCTCGTGATCCGCCCGCCTTGGCCTCCCAAA_GTGCTGGGATTATAGGCGTGAGCCACCGCCCG CT C MRPS16 Ensembl:ENSG00000182180 Protein coding exon GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1359943489 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_8172671,Human_RBP_ID_11422951,Human_RBP_ID_22369591,Human_RBP_ID_24831898,Human_RBP_ID_26396691 RMVar_hsa_circ_82619,RMVar_hsa_circ_127977,RMVar_hsa_circ_144275,RMVar_hsa_circ_144276 22442 RMVar_ID_22442 Human_SNP_ID_437657971 A-to-I Human chr10 - 73249994 73249994 73249994 ACCATGTTATCCAGGATGGTTTTGATCTCCTGACCTCGTGATCCGCCCGCCTTGGCCTCCCAAAA ACCATGTTATCCAGGATGGTTTTGATCTCCTGCCCTCGTGATCCGCCCGCCTTGGCCTCCCAAAA T G MRPS16 Ensembl:ENSG00000182180 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1008472074 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11422952,Human_RBP_ID_23152767,Human_RBP_ID_23468509 RMVar_hsa_circ_82619,RMVar_hsa_circ_127977,RMVar_hsa_circ_144275,RMVar_hsa_circ_144276 22443 RMVar_ID_22443 Human_SNP_ID_437657979 A-to-I Human chr10 - 73250018 73250018 73250018 TATTTTTAGTAGAGATGGGGTTTCACCATGTTATCCAGGATGGTTTTGATCTCCTGACCTCGTGA TATTTTTAGTAGAGATGGGGTTTCACCATGTTGTCCAGGATGGTTTTGATCTCCTGACCTCGTGA T C MRPS16 Ensembl:ENSG00000182180 Protein coding exon GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1273365325 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4143351,Human_RBP_ID_11422952,Human_RBP_ID_23468509,Human_RBP_ID_24831899,Human_RBP_ID_27194954 RMVar_hsa_circ_82619,RMVar_hsa_circ_127977,RMVar_hsa_circ_144275,RMVar_hsa_circ_144276 22444 RMVar_ID_22444 Human_SNP_ID_437657981 A-to-I Human chr10 - 73250023 73250022 73250023 TTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTATCCAGGATGGTTTTGATCTCCTGACCT TTTTGTATTTTTAGTAGAGATGGGGTTTCACC_TGTTATCCAGGATGGTTTTGATCTCCTGACCT AT A MRPS16 Ensembl:ENSG00000182180 Protein coding exon GSE38233;GSE107867;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;ASD brains,frontal_cortex;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,30559470,32596459 RNA-Seq:(High) rs1240068891 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_11422954 RMVar_hsa_circ_82619,RMVar_hsa_circ_127977,RMVar_hsa_circ_144275,RMVar_hsa_circ_144276 22445 RMVar_ID_22445 Human_SNP_ID_437657982 A-to-I Human chr10 - 73250023 73250023 73250023 TTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTATCCAGGATGGTTTTGATCTCCTGACCT TTTTGTATTTTTAGTAGAGATGGGGTTTCACCGTGTTATCCAGGATGGTTTTGATCTCCTGACCT T C MRPS16 Ensembl:ENSG00000182180 Protein coding exon GSE38233;GSE107867;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;ASD brains,frontal_cortex;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,30559470,32596459 RNA-Seq:(High) rs1370853039 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11422954 RMVar_hsa_circ_82619,RMVar_hsa_circ_127977,RMVar_hsa_circ_144275,RMVar_hsa_circ_144276 22446 RMVar_ID_22446 Human_SNP_ID_437658004 A-to-I Human chr10 - 73250084 73250084 73250084 TCCCGAGTAGTCCCAGGAGTAGCTGGGACTACAGGTGCCCACCACCACACCCAGCTAATTTTTTT TCCCGAGTAGTCCCAGGAGTAGCTGGGACTACGGGTGCCCACCACCACACCCAGCTAATTTTTTT T C MRPS16 Ensembl:ENSG00000182180 Protein coding exon GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,31158229,32596459,32596459 RNA-Seq:(High) rs539672097 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5998348,Human_RBP_ID_17680601,Human_RBP_ID_17782284,Human_RBP_ID_23152769,Human_RBP_ID_26396693 RMVar_hsa_circ_82619,RMVar_hsa_circ_127977,RMVar_hsa_circ_144275,RMVar_hsa_circ_144276 22447 RMVar_ID_22447 Human_SNP_ID_437658023 A-to-I Human chr10 - 73250157 73250149 73250158 TGAGTGCAGTGGCGCGATCTCGGCTCACTGCAAGCTCTGTCTCCTGGGTTCATGCCATTCTCCTG TGAGTGCAGTGGCGCGATCTCGGCTCACTGC_________CTCCTGGGTTCATGCCATTCTCCTG GACAGAGCTT G MRPS16 Ensembl:ENSG00000182180 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1241143467 Functional Loss DEL dbSNP153 32..40 33 - - - RMVar_hsa_circ_82619,RMVar_hsa_circ_127977,RMVar_hsa_circ_144275,RMVar_hsa_circ_144276 22448 RMVar_ID_22448 Human_SNP_ID_437658064 A-to-I Human chr10 - 73250259 73250259 73250259 GCCTCAGCCTCCTGAGTAGCCGGGGAGCTACAAGCATGCACCACCACACCCAGCTAATTTTTTTT GCCTCAGCCTCCTGAGTAGCCGGGGAGCTACAGGCATGCACCACCACACCCAGCTAATTTTTTTT T C MRPS16 Ensembl:ENSG00000182180 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886047193 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23152773 Clinvar_Rec_83 RMVar_hsa_circ_82619,RMVar_hsa_circ_127977,RMVar_hsa_circ_144275,RMVar_hsa_circ_144276 22449 RMVar_ID_22449 Human_SNP_ID_437658079 A-to-I Human chr10 - 73250329 73250329 73250329 CAGGCTGGAGTGCGGTGGTGCAATCTCAGCTCACTGCAATCTCCACCTCCTGGGTTCAAGAGGTT CAGGCTGGAGTGCGGTGGTGCAATCTCAGCTCGCTGCAATCTCCACCTCCTGGGTTCAAGAGGTT T C MRPS16 Ensembl:ENSG00000182180 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-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 22450 RMVar_ID_22450 Human_SNP_ID_437684935 A-to-I Human chr10 - 73367688 73367688 73367688 CCTAGGCAGGTGAAACACAAGGTCAACAGTTCAAGACCGGCCTGGCCAACACAGTGGGACAACTC CCTAGGCAGGTGAAACACAAGGTCAACAGTTCGAGACCGGCCTGGCCAACACAGTGGGACAACTC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs916458902 Functional Loss SNV dbSNP153 33..33 33 - - - 22451 RMVar_ID_22451 Human_SNP_ID_437686962 A-to-I Human chr10 - 73375748 73375746 73375749 TTCTGTGTAATAATATTGAATAATTTTTTAGAAGGTTACTGAAAGCTCTGCCTTCCGGAATCCCT TTCTGTGTAATAATATTGAATAATTTTTTAG___GTTACTGAAAGCTCTGCCTTCCGGAATCCCT CCTT C ANXA7 Ensembl:ENSG00000138279 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1445423079 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_382199,Human_RBP_ID_2231104,Human_RBP_ID_3356871,Human_RBP_ID_5998517,Human_RBP_ID_8338811,Human_RBP_ID_11423213,Human_RBP_ID_18243886 Human_miRNA_ID_1772569 22452 RMVar_ID_22452 Human_SNP_ID_437686964 A-to-I Human chr10 - 73375748 73375748 73375748 TTCTGTGTAATAATATTGAATAATTTTTTAGAAGGTTACTGAAAGCTCTGCCTTCCGGAATCCCT TTCTGTGTAATAATATTGAATAATTTTTTAGAGGGTTACTGAAAGCTCTGCCTTCCGGAATCCCT T C ANXA7 Ensembl:ENSG00000138279 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs939161377 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_382199,Human_RBP_ID_2231104,Human_RBP_ID_3356871,Human_RBP_ID_5998517,Human_RBP_ID_8338811,Human_RBP_ID_11423213,Human_RBP_ID_18243886 Human_miRNA_ID_1772569 22453 RMVar_ID_22453 Human_SNP_ID_437687392 A-to-I Human chr10 - 73377536 73377536 73377536 AGATGGAGTCTCGCTCTGTCACCCAGGCTGAAATACAGTGGCATAATCTCGGCTTACTGCAACCT AGATGGAGTCTCGCTCTGTCACCCAGGCTGAAGTACAGTGGCATAATCTCGGCTTACTGCAACCT T C ANXA7 Ensembl:ENSG00000138279 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1564519217 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1146180,Human_Splice_Rec_1146181 22454 RMVar_ID_22454 Human_SNP_ID_437687393 A-to-I Human chr10 - 73377538 73377538 73377538 TGAGATGGAGTCTCGCTCTGTCACCCAGGCTGAAATACAGTGGCATAATCTCGGCTTACTGCAAC TGAGATGGAGTCTCGCTCTGTCACCCAGGCTGGAATACAGTGGCATAATCTCGGCTTACTGCAAC T C ANXA7 Ensembl:ENSG00000138279 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1564519220 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1146180,Human_Splice_Rec_1146181 22455 RMVar_ID_22455 Human_SNP_ID_437695368 A-to-I Human chr10 - 73408273 73408273 73408273 GTCTTTTCTTTCAACTGGAGTGCAATGATGCAAACACGACTCACTGCCGCCTTGACCTCCTGGCC GTCTTTTCTTTCAACTGGAGTGCAATGATGCAGACACGACTCACTGCCGCCTTGACCTCCTGGCC T C ANXA7 Ensembl:ENSG00000138279 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs952054573 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19545165 Human_Splice_Rec_1146197 RMVar_hsa_circ_76614,RMVar_hsa_circ_107453,RMVar_hsa_circ_144284,RMVar_hsa_circ_144293,RMVar_hsa_circ_84558,RMVar_hsa_circ_144296 22456 RMVar_ID_22456 Human_SNP_ID_437695887 A-to-I Human chr10 - 73410600 73410600 73410600 TTTTGTTATTTTTGGTAGAGACGGGTTTCTCCATGTTGGTCAGGCTGGTTTCAAACTCCCAACCT TTTTGTTATTTTTGGTAGAGACGGGTTTCTCCCTGTTGGTCAGGCTGGTTTCAAACTCCCAACCT T G ANXA7 Ensembl:ENSG00000138279 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900578962 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76614,RMVar_hsa_circ_107453,RMVar_hsa_circ_144284,RMVar_hsa_circ_144293,RMVar_hsa_circ_84558,RMVar_hsa_circ_144296 22457 RMVar_ID_22457 Human_SNP_ID_437698991 A-to-I Human chr10 + 73422715 73422715 73422715 GGATTAAACTTCATTTTGGCCGCTCCTGCTTCAGTGATGGCCGCAAGAGGGAAGAGAGCTCTTTT GGATTAAACTTCATTTTGGCCGCTCCTGCTTCCGTGATGGCCGCAAGAGGGAAGAGAGCTCTTTT A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs528734214 Functional Loss SNV dbSNP153 33..33 33 - - - 22458 RMVar_ID_22458 Human_SNP_ID_437706159 A-to-I Human chr10 - 73451874 73451874 73451874 GGTCGTTGTGGTGGGTGCTTGTAGTCCTAGCTACTTGGGAGGCTGGGGCAGGAGAATACAGTGAA GGTCGTTGTGGTGGGTGCTTGTAGTCCTAGCTGCTTGGGAGGCTGGGGCAGGAGAATACAGTGAA T C PPP3CB Ensembl:ENSG00000107758 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232777063 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_385,RMVar_hsa_circ_87356,RMVar_hsa_circ_144299,RMVar_hsa_circ_304594,RMVar_hsa_circ_144302,RMVar_hsa_circ_297628,RMVar_hsa_circ_144301,RMVar_hsa_circ_339419,RMVar_hsa_circ_286011 22459 RMVar_ID_22459 Human_SNP_ID_437706181 A-to-I Human chr10 - 73451940 73451939 73451940 AGATCAAGACCATCCTGGCTTAACATGGTGAAACCCTGTCTCTACCAAAAATACAAAAAATTAGC AGATCAAGACCATCCTGGCTTAACATGGTGAA_CCCTGTCTCTACCAAAAATACAAAAAATTAGC GT G PPP3CB Ensembl:ENSG00000107758 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1265452761 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_385,RMVar_hsa_circ_87356,RMVar_hsa_circ_144299,RMVar_hsa_circ_304594,RMVar_hsa_circ_144302,RMVar_hsa_circ_297628,RMVar_hsa_circ_144301,RMVar_hsa_circ_339419,RMVar_hsa_circ_286011 22460 RMVar_ID_22460 Human_SNP_ID_437706182 A-to-I Human chr10 - 73451940 73451940 73451940 AGATCAAGACCATCCTGGCTTAACATGGTGAAACCCTGTCTCTACCAAAAATACAAAAAATTAGC AGATCAAGACCATCCTGGCTTAACATGGTGAAGCCCTGTCTCTACCAAAAATACAAAAAATTAGC T C PPP3CB Ensembl:ENSG00000107758 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs996527636 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_385,RMVar_hsa_circ_87356,RMVar_hsa_circ_144299,RMVar_hsa_circ_304594,RMVar_hsa_circ_144302,RMVar_hsa_circ_297628,RMVar_hsa_circ_144301,RMVar_hsa_circ_339419,RMVar_hsa_circ_286011 22461 RMVar_ID_22461 Human_SNP_ID_437713086 A-to-I Human chr10 - 73480601 73480601 73480601 GTCTCTACTAAAAATACAAAAATAAGCTGGGCATGATGGCGGATGCCTGTAATCCCAGCTACTCG GTCTCTACTAAAAATACAAAAATAAGCTGGGCGTGATGGCGGATGCCTGTAATCCCAGCTACTCG T C PPP3CB Ensembl:ENSG00000107758 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1186235506 Functional Loss SNV dbSNP153 33..33 33 - - - 22462 RMVar_ID_22462 Human_SNP_ID_437713258 A-to-I Human chr10 - 73481246 73481246 73481246 GCTGGTCTTGAACTCCTGACTTCAAGTGATCCACTGGCCTTGGCCTCCCAAGTCTGGGATTTCAG GCTGGTCTTGAACTCCTGACTTCAAGTGATCCGCTGGCCTTGGCCTCCCAAGTCTGGGATTTCAG T C PPP3CB Ensembl:ENSG00000107758 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs528709868 Functional Loss SNV dbSNP153 33..33 33 - - - 22463 RMVar_ID_22463 Human_SNP_ID_437713259 A-to-I Human chr10 - 73481246 73481246 73481246 GCTGGTCTTGAACTCCTGACTTCAAGTGATCCACTGGCCTTGGCCTCCCAAGTCTGGGATTTCAG GCTGGTCTTGAACTCCTGACTTCAAGTGATCCCCTGGCCTTGGCCTCCCAAGTCTGGGATTTCAG T G PPP3CB Ensembl:ENSG00000107758 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs528709868 Functional Loss SNV dbSNP153 33..33 33 - - - 22464 RMVar_ID_22464 Human_SNP_ID_437713784 A-to-I Human chr10 - 73482913 73482913 73482913 TTGGTTGTTAGGAAGTATATATCATCTAGGCCAGGCACAGTGGCTGACGCTTGTAATCCCAACAC TTGGTTGTTAGGAAGTATATATCATCTAGGCCGGGCACAGTGGCTGACGCTTGTAATCCCAACAC T C PPP3CB Ensembl:ENSG00000107758 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1303789525 Functional Loss SNV dbSNP153 33..33 33 - - - 22465 RMVar_ID_22465 Human_SNP_ID_437714043 A-to-I Human chr10 - 73483964 73483964 73483964 AATTTTTGTGTTTTTAGTAGCGATGGGGTTTCACTATGTTGGCCAGGATGGTCTTGAACTCCTGA AATTTTTGTGTTTTTAGTAGCGATGGGGTTTCGCTATGTTGGCCAGGATGGTCTTGAACTCCTGA T C PPP3CB Ensembl:ENSG00000107758 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1292393924 Functional Loss SNV dbSNP153 33..33 33 - - - 22466 RMVar_ID_22466 Human_SNP_ID_437714067 A-to-I Human chr10 - 73484030 73484030 73484030 TCAAGCGATTCTTGTGCCTCAGCCTCCAAAGTAGCTGGGACTACAGGCGCGACACCACACCTGGC TCAAGCGATTCTTGTGCCTCAGCCTCCAAAGTGGCTGGGACTACAGGCGCGACACCACACCTGGC T C PPP3CB Ensembl:ENSG00000107758 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs148354270 Functional Loss SNV dbSNP153 33..33 33 - - - 22467 RMVar_ID_22467 Human_SNP_ID_437714075 A-to-I Human chr10 - 73484059 73484059 73484059 AGCTCACTACAACCTCCACCCCACCAGGTTCAAGCGATTCTTGTGCCTCAGCCTCCAAAGTAGCT AGCTCACTACAACCTCCACCCCACCAGGTTCAGGCGATTCTTGTGCCTCAGCCTCCAAAGTAGCT T C PPP3CB Ensembl:ENSG00000107758 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs888504578 Functional Loss SNV dbSNP153 33..33 33 - - - 22468 RMVar_ID_22468 Human_SNP_ID_437714086 A-to-I Human chr10 - 73484091 73484091 73484091 TTGCCCAGGCTAGAGTTCAGTGGCACGATCTCAGCTCACTACAACCTCCACCCCACCAGGTTCAA TTGCCCAGGCTAGAGTTCAGTGGCACGATCTCGGCTCACTACAACCTCCACCCCACCAGGTTCAA T C PPP3CB Ensembl:ENSG00000107758 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005969716 Functional Loss SNV dbSNP153 33..33 33 - - - 22469 RMVar_ID_22469 Human_SNP_ID_437715141 A-to-I Human chr10 - 73487385 73487385 73487385 TGCCACCACGCCCCGCTAATTTTTGTATTTTTAGTAGAGACGGGATTTCGCCATGTTGGCCAGGC TGCCACCACGCCCCGCTAATTTTTGTATTTTTGGTAGAGACGGGATTTCGCCATGTTGGCCAGGC T C PPP3CB Ensembl:ENSG00000107758 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1274178158 Functional Loss SNV dbSNP153 33..33 33 - - - 22470 RMVar_ID_22470 Human_SNP_ID_437716330 A-to-I Human chr10 - 73491751 73491727 73491751 GTTGGTCAGGCTGGTCTCGATCTCCTGACCTCAGGTGATCCACCCACCCTGGCCTCCCAAAATGC GTTGGTCAGGCTGGTCTCGATCTCCTGACCTC________________________CCAAAATGC GGAGGCCAGGGTGGGTGGATCACCT G PPP3CB Ensembl:ENSG00000107758 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1441503504 Functional Loss DEL dbSNP153 33..56 33 - - - 22471 RMVar_ID_22471 Human_SNP_ID_437716995 A-to-I Human chr10 - 73494452 73494442 73494452 TTTCTCTACCAAAAATACAAAAAATAAAAATTAGCCGGGCATGGTGGCGCGCCCCTGTAGTCCCA TTTCTCTACCAAAAATACAAAAAATAAAAATT__________GGTGGCGCGCCCCTGTAGTCCCA CATGCCCGGCT C PPP3CB Ensembl:ENSG00000107758 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1305764103 Functional Loss DEL dbSNP153 33..42 33 - - - 22472 RMVar_ID_22472 Human_SNP_ID_437716997 A-to-I Human chr10 - 73494452 73494446 73494453 TTTCTCTACCAAAAATACAAAAAATAAAAATTAGCCGGGCATGGTGGCGCGCCCCTGTAGTCCCA TTTCTCTACCAAAAATACAAAAAATAAAAAT_______GCATGGTGGCGCGCCCCTGTAGTCCCA CCCGGCTA C PPP3CB Ensembl:ENSG00000107758 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1247890673 Functional Loss DEL dbSNP153 32..38 33 - - - 22473 RMVar_ID_22473 Human_SNP_ID_437720285 A-to-I Human chr10 - 73508145 73508145 73508145 GCCTCGCCTCCCAAAGTGTTGGGATTACAGGCATGAGCCATCGCACCCTGCCTTCTTTTAAAGGA GCCTCGCCTCCCAAAGTGTTGGGATTACAGGCCTGAGCCATCGCACCCTGCCTTCTTTTAAAGGA T G USP54 Ensembl:ENSG00000166348 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs531062813 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91450,RMVar_hsa_circ_110450,RMVar_hsa_circ_144318,RMVar_hsa_circ_144319 22474 RMVar_ID_22474 Human_SNP_ID_437730193 A-to-I Human chr10 - 73550078 73550078 73550078 CTCTACTAAAAATGCAAAACTTAGCCGGGTGTAGTGGCACATACCTGTAATCCCAGCTACTTGGG CTCTACTAAAAATGCAAAACTTAGCCGGGTGTGGTGGCACATACCTGTAATCCCAGCTACTTGGG T C USP54 Ensembl:ENSG00000166348 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1423393647 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91450,RMVar_hsa_circ_144319,RMVar_hsa_circ_65447,RMVar_hsa_circ_378301,RMVar_hsa_circ_348115,RMVar_hsa_circ_302703,RMVar_hsa_circ_333890,RMVar_hsa_circ_14153,RMVar_hsa_circ_144328,RMVar_hsa_circ_118124,RMVar_hsa_circ_87160,RMVar_hsa_circ_144333,RMVar_hsa_circ_144334,RMVar_hsa_circ_144335,RMVar_hsa_circ_47633,RMVar_hsa_circ_324874 22475 RMVar_ID_22475 Human_SNP_ID_437730201 A-to-I Human chr10 - 73550103 73550103 73550103 CCTGGCCAACATAGCAAAACCCGGCCTCTACTAAAAATGCAAAACTTAGCCGGGTGTAGTGGCAC CCTGGCCAACATAGCAAAACCCGGCCTCTACTGAAAATGCAAAACTTAGCCGGGTGTAGTGGCAC T C USP54 Ensembl:ENSG00000166348 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1002576268 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91450,RMVar_hsa_circ_144319,RMVar_hsa_circ_65447,RMVar_hsa_circ_378301,RMVar_hsa_circ_348115,RMVar_hsa_circ_302703,RMVar_hsa_circ_333890,RMVar_hsa_circ_14153,RMVar_hsa_circ_144328,RMVar_hsa_circ_118124,RMVar_hsa_circ_87160,RMVar_hsa_circ_144333,RMVar_hsa_circ_144334,RMVar_hsa_circ_144335,RMVar_hsa_circ_47633,RMVar_hsa_circ_324874 22476 RMVar_ID_22476 Human_SNP_ID_437737761 A-to-I Human chr10 - 73583697 73583697 73583697 TCACCCTGGCTGGAGTGCAGTGGCACAGTCATAGCTCACTACAGGCTTGAATTTCCAGGCTCAAA TCACCCTGGCTGGAGTGCAGTGGCACAGTCATGGCTCACTACAGGCTTGAATTTCCAGGCTCAAA T C USP54 Ensembl:ENSG00000166348 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1035599635 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87160,RMVar_hsa_circ_144334,RMVar_hsa_circ_91310,RMVar_hsa_circ_144341,RMVar_hsa_circ_127161,RMVar_hsa_circ_144344 22477 RMVar_ID_22477 Human_SNP_ID_437737762 A-to-I Human chr10 - 73583697 73583697 73583697 TCACCCTGGCTGGAGTGCAGTGGCACAGTCATAGCTCACTACAGGCTTGAATTTCCAGGCTCAAA TCACCCTGGCTGGAGTGCAGTGGCACAGTCATCGCTCACTACAGGCTTGAATTTCCAGGCTCAAA T G USP54 Ensembl:ENSG00000166348 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1035599635 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87160,RMVar_hsa_circ_144334,RMVar_hsa_circ_91310,RMVar_hsa_circ_144341,RMVar_hsa_circ_127161,RMVar_hsa_circ_144344 22478 RMVar_ID_22478 Human_SNP_ID_437743151 A-to-I Human chr10 - 73607659 73607659 73607659 CCTGGGAAATTTTTTGCGTTTTTAGTAGATACAGGGTTTTACCATGTTGGTCAGGGTGATCTTGA CCTGGGAAATTTTTTGCGTTTTTAGTAGATACTGGGTTTTACCATGTTGGTCAGGGTGATCTTGA T A USP54 Ensembl:ENSG00000166348 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1460176262 Functional Loss SNV dbSNP153 33..33 33 - - - 22479 RMVar_ID_22479 Human_SNP_ID_437743261 A-to-I Human chr10 - 73608075 73608075 73608075 TTGTATTTTTGTTAGGGACAGGGTTTCACCATATTGCCCAGGCTGGTCTTGGACTCCTGACTTCG TTGTATTTTTGTTAGGGACAGGGTTTCACCATGTTGCCCAGGCTGGTCTTGGACTCCTGACTTCG T C USP54 Ensembl:ENSG00000166348 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs950974564 Functional Loss SNV dbSNP153 33..33 33 - - - 22480 RMVar_ID_22480 Human_SNP_ID_437743262 A-to-I Human chr10 - 73608075 73608075 73608075 TTGTATTTTTGTTAGGGACAGGGTTTCACCATATTGCCCAGGCTGGTCTTGGACTCCTGACTTCG TTGTATTTTTGTTAGGGACAGGGTTTCACCATCTTGCCCAGGCTGGTCTTGGACTCCTGACTTCG T G USP54 Ensembl:ENSG00000166348 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs950974564 Functional Loss SNV dbSNP153 33..33 33 - - - 22481 RMVar_ID_22481 Human_SNP_ID_437743430 A-to-I Human chr10 - 73608741 73608741 73608741 AGACACGCGCTAGCATGCCCTGCTAATTTTTTATATTTTTAGTAGAGACTGGGTTTCATCATGTT AGACACGCGCTAGCATGCCCTGCTAATTTTTTGTATTTTTAGTAGAGACTGGGTTTCATCATGTT T C USP54 Ensembl:ENSG00000166348 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1231592544 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11425170 22482 RMVar_ID_22482 Human_SNP_ID_437744960 A-to-I Human chr10 - 73615231 73615231 73615231 CCTCAGCCTCCTGAGTATACTCAGTTGGGATTACAGGTGGATGCCACCATGCCTGGCTAATTTTT CCTCAGCCTCCTGAGTATACTCAGTTGGGATTGCAGGTGGATGCCACCATGCCTGGCTAATTTTT T C USP54 Ensembl:ENSG00000166348 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1331818269 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5999356 22483 RMVar_ID_22483 Human_SNP_ID_437745582 A-to-I Human chr10 - 73617826 73617826 73617826 GGCTTACTGCAGCTTTTGCCTCCTGGACTCAAACAATCCTCTCACCTCAGCCTCCCAAGTAGCTG GGCTTACTGCAGCTTTTGCCTCCTGGACTCAAGCAATCCTCTCACCTCAGCCTCCCAAGTAGCTG T C USP54 Ensembl:ENSG00000166348 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1242160614 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8338896,Human_RBP_ID_11425390 22484 RMVar_ID_22484 Human_SNP_ID_437746105 A-to-I Human chr10 - 73620128 73620128 73620128 TTGTATTTTCAGTAGAGACAGAGTTTCACCATATTGGTCAGGCTCGTCTGGAACTCCTGACCTCA TTGTATTTTCAGTAGAGACAGAGTTTCACCATGTTGGTCAGGCTCGTCTGGAACTCCTGACCTCA T C USP54 Ensembl:ENSG00000166348 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1311376756 Functional Loss SNV dbSNP153 33..33 33 - - - 22485 RMVar_ID_22485 Human_SNP_ID_437767223 A-to-I Human chr10 - 73702364 73702364 73702364 TGGGAGGCCGAGGTGGGCAGATCACGAAGTCAAGAGACCGAGAACATCCTGGCTAACACAGTGAA TGGGAGGCCGAGGTGGGCAGATCACGAAGTCAGGAGACCGAGAACATCCTGGCTAACACAGTGAA T C AC022400.5,AC022400.3 Ensembl:ENSG00000271816,Ensembl:ENSG00000242288 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1135743 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11425605,Human_RBP_ID_24833022 RMVar_hsa_circ_58885,RMVar_hsa_circ_89736,RMVar_hsa_circ_144346,RMVar_hsa_circ_313877,RMVar_hsa_circ_83179,RMVar_hsa_circ_100065,RMVar_hsa_circ_104003,RMVar_hsa_circ_84866,RMVar_hsa_circ_144354,RMVar_hsa_circ_144355,RMVar_hsa_circ_144356,RMVar_hsa_circ_144353 22486 RMVar_ID_22486 Human_SNP_ID_437767225 A-to-I Human chr10 - 73702369 73702369 73702369 GACTTTGGGAGGCCGAGGTGGGCAGATCACGAAGTCAAGAGACCGAGAACATCCTGGCTAACACA GACTTTGGGAGGCCGAGGTGGGCAGATCACGAGGTCAAGAGACCGAGAACATCCTGGCTAACACA T C AC022400.5,AC022400.3 Ensembl:ENSG00000271816,Ensembl:ENSG00000242288 lincRNA,lincRNA intron,intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1002598489 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11425605,Human_RBP_ID_24833022 RMVar_hsa_circ_58885,RMVar_hsa_circ_89736,RMVar_hsa_circ_144346,RMVar_hsa_circ_313877,RMVar_hsa_circ_83179,RMVar_hsa_circ_100065,RMVar_hsa_circ_104003,RMVar_hsa_circ_84866,RMVar_hsa_circ_144354,RMVar_hsa_circ_144355,RMVar_hsa_circ_144356,RMVar_hsa_circ_144353 22487 RMVar_ID_22487 Human_SNP_ID_437767630 A-to-I Human chr10 - 73704666 73704666 73704666 GCCCTGCTAATTTTTGTGATTTTTTTTTTAGTAGAGACGAGGTTTCACTATGTAGGCAAAGCTGG GCCCTGCTAATTTTTGTGATTTTTTTTTTAGTGGAGACGAGGTTTCACTATGTAGGCAAAGCTGG T C AC022400.5,AC022400.6,AC022400.3 Ensembl:ENSG00000271816,Ensembl:ENSG00000272140,Ensembl:ENSG00000242288 lincRNA,lincRNA,lincRNA intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs531964135 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58885,RMVar_hsa_circ_89736,RMVar_hsa_circ_144346,RMVar_hsa_circ_313877,RMVar_hsa_circ_83179,RMVar_hsa_circ_100065,RMVar_hsa_circ_104003,RMVar_hsa_circ_84866,RMVar_hsa_circ_144354,RMVar_hsa_circ_144355,RMVar_hsa_circ_144356,RMVar_hsa_circ_144353 22488 RMVar_ID_22488 Human_SNP_ID_437767657 A-to-I Human chr10 - 73704792 73704792 73704792 ACTCTGTCACCCAGGCTGGAGTTCTGTGGCACAGTCTTGGCTCACTGCAACCTCCGCCTGCCGGG ACTCTGTCACCCAGGCTGGAGTTCTGTGGCACGGTCTTGGCTCACTGCAACCTCCGCCTGCCGGG T C AC022400.5,AC022400.6,AC022400.3 Ensembl:ENSG00000271816,Ensembl:ENSG00000272140,Ensembl:ENSG00000242288 lincRNA,lincRNA,lincRNA intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1317196754 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8173734,Human_RBP_ID_26882105 RMVar_hsa_circ_58885,RMVar_hsa_circ_89736,RMVar_hsa_circ_144346,RMVar_hsa_circ_313877,RMVar_hsa_circ_83179,RMVar_hsa_circ_100065,RMVar_hsa_circ_104003,RMVar_hsa_circ_84866,RMVar_hsa_circ_144354,RMVar_hsa_circ_144355,RMVar_hsa_circ_144356,RMVar_hsa_circ_144353 22489 RMVar_ID_22489 Human_SNP_ID_437775838 A-to-I Human chr10 + 73741322 73741322 73741322 AAGAGTGGTGGCACATGCCTGTAGTCCCAGCTACTAGGGAGGCTGAGTGGGGAGGATCACTTGAG AAGAGTGGTGGCACATGCCTGTAGTCCCAGCTGCTAGGGAGGCTGAGTGGGGAGGATCACTTGAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1420342145 Functional Loss SNV dbSNP153 33..33 33 - - - 22490 RMVar_ID_22490 Human_SNP_ID_437778624 A-to-I Human chr10 + 73752170 73752170 73752170 TTGAGACAGGGTCTCACTCCGTGGCCCAAGCTAGAGTGCAGTGGCAGGATCACAACTCCCTGGAG TTGAGACAGGGTCTCACTCCGTGGCCCAAGCTGGAGTGCAGTGGCAGGATCACAACTCCCTGGAG A G SEC24C Ensembl:ENSG00000176986 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1404071931 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60050,RMVar_hsa_circ_126838,RMVar_hsa_circ_42416,RMVar_hsa_circ_144369 22491 RMVar_ID_22491 Human_SNP_ID_437778646 A-to-I Human chr10 + 73752261 73752261 73752261 CTCCCACCTCAGTTTCCCAGGTAGCTGGGACTACAGGCATGCGCCACCACACCCAGCTAATTTTT CTCCCACCTCAGTTTCCCAGGTAGCTGGGACTGCAGGCATGCGCCACCACACCCAGCTAATTTTT A G SEC24C Ensembl:ENSG00000176986 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs973593749 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60050,RMVar_hsa_circ_126838,RMVar_hsa_circ_42416,RMVar_hsa_circ_144369 22492 RMVar_ID_22492 Human_SNP_ID_437779362 A-to-I Human chr10 + 73755514 73755514 73755514 CCTGGCTAACACGGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTAGCTGGGCGCGGTGGCA CCTGGCTAACACGGTGAAACCCCGTCTCTACTGAAAATACAAAAAATTAGCTGGGCGCGGTGGCA A G SEC24C Ensembl:ENSG00000176986 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1194614610 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60050,RMVar_hsa_circ_126838,RMVar_hsa_circ_42416,RMVar_hsa_circ_144369 22493 RMVar_ID_22493 Human_SNP_ID_437779500 A-to-I Human chr10 + 73756026 73756026 73756026 GATGTGGGCCACCATGCCCGGCTAATTTTTGTATTTTTAGTAGAGATGAGGTTTCACCGTGTTGG GATGTGGGCCACCATGCCCGGCTAATTTTTGTGTTTTTAGTAGAGATGAGGTTTCACCGTGTTGG A G SEC24C Ensembl:ENSG00000176986 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1461384767 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60050,RMVar_hsa_circ_126838,RMVar_hsa_circ_42416,RMVar_hsa_circ_144369 22494 RMVar_ID_22494 Human_SNP_ID_437779660 A-to-I Human chr10 + 73756784 73756784 73756784 ACCATGCCAGGCTAATTTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGG ACCATGCCAGGCTAATTTTTTGTATTTTTAGTGGAGACAGGGTTTCACCATGTTGGCCAGGCTGG A G SEC24C Ensembl:ENSG00000176986 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1325621255 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60050,RMVar_hsa_circ_126838,RMVar_hsa_circ_42416,RMVar_hsa_circ_144369 22495 RMVar_ID_22495 Human_SNP_ID_437779811 A-to-I Human chr10 + 73757295 73757295 73757295 GTAGTAATCTCAACACCTTGGGAGGCTGAGACAGGAGGATCACTTGAGGCCAGAAGTTTTAGACC GTAGTAATCTCAACACCTTGGGAGGCTGAGACGGGAGGATCACTTGAGGCCAGAAGTTTTAGACC A G SEC24C Ensembl:ENSG00000176986 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1034495414 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60050,RMVar_hsa_circ_126838,RMVar_hsa_circ_42416,RMVar_hsa_circ_144369 22496 RMVar_ID_22496 Human_SNP_ID_437779847 A-to-I Human chr10 + 73757429 73757429 73757429 TGGGAAGCAGAGGTGGAGGCAGGAGGATTGCTAGAGCCCTGGAGGTTGAGGCTACAGTGAGCCAT TGGGAAGCAGAGGTGGAGGCAGGAGGATTGCTGGAGCCCTGGAGGTTGAGGCTACAGTGAGCCAT A G SEC24C Ensembl:ENSG00000176986 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1341588149 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60050,RMVar_hsa_circ_126838,RMVar_hsa_circ_42416,RMVar_hsa_circ_144369 22497 RMVar_ID_22497 Human_SNP_ID_437780047 A-to-I Human chr10 + 73757980 73757980 73757980 ACGTAAGGCTGGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGTTGAGGCGGGCGA ACGTAAGGCTGGGCACGGTGGCTCACGCCTGTGATCCCAGCACTTTGGGAGGTTGAGGCGGGCGA A G SEC24C Ensembl:ENSG00000176986 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1485267184 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60050,RMVar_hsa_circ_126838,RMVar_hsa_circ_42416,RMVar_hsa_circ_144369 22498 RMVar_ID_22498 Human_SNP_ID_437785551 A-to-I Human chr10 + 73776534 73776534 73776534 GCAAGACCTTGTCTCTAAAAAATAAAAGAATTAGCAGGGCATGGTGGTGCACACCTGTAGCCCTA GCAAGACCTTGTCTCTAAAAAATAAAAGAATTTGCAGGGCATGGTGGTGCACACCTGTAGCCCTA A T FUT11 Ensembl:ENSG00000196968 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1336396587 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11426113,Human_RBP_ID_26398437 22499 RMVar_ID_22499 Human_SNP_ID_437785555 A-to-I Human chr10 + 73776537 73776537 73776537 AGACCTTGTCTCTAAAAAATAAAAGAATTAGCAGGGCATGGTGGTGCACACCTGTAGCCCTAGAT AGACCTTGTCTCTAAAAAATAAAAGAATTAGCGGGGCATGGTGGTGCACACCTGTAGCCCTAGAT A G FUT11 Ensembl:ENSG00000196968 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs970300753 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26398437 22500 RMVar_ID_22500 Human_SNP_ID_437785577 A-to-I Human chr10 + 73776664 73776664 73776664 GATCATGATCACTGCACTCCAGCCTGGGTGACAGAGCGAGACACCGTCTCAAATTATATATATAT GATCATGATCACTGCACTCCAGCCTGGGTGACGGAGCGAGACACCGTCTCAAATTATATATATAT A G FUT11 Ensembl:ENSG00000196968 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs879666137 Functional Loss SNV dbSNP153 33..33 33 - - - 22501 RMVar_ID_22501 Human_SNP_ID_437785621 A-to-I Human chr10 + 73776797 73776797 73776797 CACCTCCCTGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCATGCA CACCTCCCTGGTTCAAGCGATTCTCCTGCCTCGGCCTCCTGAGTAGCTGGGACTACAGGCATGCA A G FUT11 Ensembl:ENSG00000196968 Protein coding intron GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,31158229,31158229 RNA-Seq:(High) rs1298841893 Functional Loss SNV dbSNP153 33..33 33 - - - 22502 RMVar_ID_22502 Human_SNP_ID_437785623 A-to-I Human chr10 + 73776825 73776825 73776825 CCTCAGCCTCCTGAGTAGCTGGGACTACAGGCATGCACCACCACGCCCAGCTAATTTTTTGTATT CCTCAGCCTCCTGAGTAGCTGGGACTACAGGCGTGCACCACCACGCCCAGCTAATTTTTTGTATT A G FUT11 Ensembl:ENSG00000196968 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1426527656 Functional Loss SNV dbSNP153 33..33 33 - - - 22503 RMVar_ID_22503 Human_SNP_ID_437785636 A-to-I Human chr10 + 73776870 73776869 73776871 CCCAGCTAATTTTTTGTATTTCTAGTAGAGACAGGGTTTCGCCATGTTGGCAAGGATAGTCTCGA CCCAGCTAATTTTTTGTATTTCTAGTAGAGAC__GGTTTCGCCATGTTGGCAAGGATAGTCTCGA CAG C FUT11 Ensembl:ENSG00000196968 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1222721702 Functional Loss DEL dbSNP153 33..34 33 - - - 22504 RMVar_ID_22504 Human_SNP_ID_437785646 A-to-I Human chr10 + 73776895 73776895 73776895 TAGAGACAGGGTTTCGCCATGTTGGCAAGGATAGTCTCGATTTCTTGACTTCGTGATCCGCCCGC TAGAGACAGGGTTTCGCCATGTTGGCAAGGATGGTCTCGATTTCTTGACTTCGTGATCCGCCCGC A G FUT11 Ensembl:ENSG00000196968 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1130778 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26399077 22505 RMVar_ID_22505 Human_SNP_ID_437785666 A-to-I Human chr10 + 73776953 73776953 73776953 CGCCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGTGTCAGCCACCGCACCCGGCCTCAAATA CGCCCGCCTTGGCCTCCCAAAGTGCTGGGATTGCAGGTGTCAGCCACCGCACCCGGCCTCAAATA A G FUT11 Ensembl:ENSG00000196968 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs3190020 Functional Loss SNV dbSNP153 33..33 33 - - - 22506 RMVar_ID_22506 Human_SNP_ID_437785835 A-to-I Human chr10 + 73777654 73777654 73777654 TCAGCTTACTAGAATCTCTGCATTCCCAGTTCAAGTGATTCTCCTGCCTCAGCCTCCCTAGTAGT TCAGCTTACTAGAATCTCTGCATTCCCAGTTCGAGTGATTCTCCTGCCTCAGCCTCCCTAGTAGT A G FUT11 Ensembl:ENSG00000196968 Protein coding intron GSE38233;GSE100210;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1203219391 Functional Loss SNV dbSNP153 33..33 33 - - - 22507 RMVar_ID_22507 Human_SNP_ID_437785838 A-to-I Human chr10 + 73777659 73777659 73777659 TTACTAGAATCTCTGCATTCCCAGTTCAAGTGATTCTCCTGCCTCAGCCTCCCTAGTAGTGGGGA TTACTAGAATCTCTGCATTCCCAGTTCAAGTGTTTCTCCTGCCTCAGCCTCCCTAGTAGTGGGGA A T FUT11 Ensembl:ENSG00000196968 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1038525942 Functional Loss SNV dbSNP153 33..33 33 - - - 22508 RMVar_ID_22508 Human_SNP_ID_437785853 A-to-I Human chr10 + 73777720 73777720 73777720 GGGATTACAGGCGCCCGTCACCACATCTAGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCA GGGATTACAGGCGCCCGTCACCACATCTAGCTTATTTTTGTATTTTTAGTAGAGATGGGGTTTCA A T FUT11 Ensembl:ENSG00000196968 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs890753819 Functional Loss SNV dbSNP153 33..33 33 - - - 22509 RMVar_ID_22509 Human_SNP_ID_437785915 A-to-I Human chr10 + 73777908 73777908 73777908 TTGAGGCAGAGTCTCACTCCATCACCAAGGCTAGAGTGCAGTGGCGTGATTTTGGCTCACTGCAG TTGAGGCAGAGTCTCACTCCATCACCAAGGCTTGAGTGCAGTGGCGTGATTTTGGCTCACTGCAG A T FUT11 Ensembl:ENSG00000196968 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs1316348112 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8992169 22510 RMVar_ID_22510 Human_SNP_ID_437785924 A-to-I Human chr10 + 73777959 73777959 73777959 TTGGCTCACTGCAGCCTCTGCCTCCCAGGTTCAAGCAATTCTCGTGTCTCAGCCTCCAGAGTGGT TTGGCTCACTGCAGCCTCTGCCTCCCAGGTTCCAGCAATTCTCGTGTCTCAGCCTCCAGAGTGGT A C FUT11 Ensembl:ENSG00000196968 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1207571964 Functional Loss SNV dbSNP153 33..33 33 - - - 22511 RMVar_ID_22511 Human_SNP_ID_437786026 A-to-I Human chr10 + 73778380 73778379 73778380 GCACCATTGCACTCCAGCCTGGGTGACGAGCGAAACTCCATCCCAAAAAAAAAAAAAAAAAAAAA GCACCATTGCACTCCAGCCTGGGTGACGAGCG_AACTCCATCCCAAAAAAAAAAAAAAAAAAAAA GA G FUT11 Ensembl:ENSG00000196968 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1159531186 Functional Loss DEL dbSNP153 33..33 33 - - - 22512 RMVar_ID_22512 Human_SNP_ID_437786163 A-to-I Human chr10 + 73778937 73778937 73778937 AAGGTAGGAGGATCGCTTGAGCCCAGGGATTCAAGACCAGCTTGGGTAACATGGTAAAACCCCAT AAGGTAGGAGGATCGCTTGAGCCCAGGGATTCGAGACCAGCTTGGGTAACATGGTAAAACCCCAT A G FUT11 Ensembl:ENSG00000196968 Protein coding exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1134778 Functional Loss SNV dbSNP153 33..33 33 - - - 22513 RMVar_ID_22513 Human_SNP_ID_437786165 A-to-I Human chr10 + 73778943 73778943 73778943 GGAGGATCGCTTGAGCCCAGGGATTCAAGACCAGCTTGGGTAACATGGTAAAACCCCATCTCTAC GGAGGATCGCTTGAGCCCAGGGATTCAAGACCGGCTTGGGTAACATGGTAAAACCCCATCTCTAC A G FUT11 Ensembl:ENSG00000196968 Protein coding exon GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1134779 Functional Loss SNV dbSNP153 33..33 33 - - - 22514 RMVar_ID_22514 Human_SNP_ID_437786291 A-to-I Human chr10 + 73779335 73779335 73779335 CCTGTAATCCCAGCACTCTGGGAGGCCAAGGCAGGCAGACCACCTGAAGTCGGGAGTTCAAGACC CCTGTAATCCCAGCACTCTGGGAGGCCAAGGCGGGCAGACCACCTGAAGTCGGGAGTTCAAGACC A G FUT11 Ensembl:ENSG00000196968 Protein coding exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1171884536 Functional Loss SNV dbSNP153 33..33 33 - - - 22515 RMVar_ID_22515 Human_SNP_ID_437794216 A-to-I Human chr10 - 73805345 73805344 73805345 CACGCCCGGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGTCAGGCTGGTC CACGCCCGGCTAATTTTTTGTATTTTTAGTAG_GACGGGGTTTCACCATGTTGGTCAGGCTGGTC CT C AC022400.7,NDST2 Ensembl:ENSG00000272916,Ensembl:ENSG00000166507 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1474212659 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_330465,RMVar_hsa_circ_367352,RMVar_hsa_circ_144389,RMVar_hsa_circ_89928 22516 RMVar_ID_22516 Human_SNP_ID_437794246 A-to-I Human chr10 - 73805467 73805467 73805467 CTCTGTCACCCAGGCTAGAGTACAATGGCACAATCTCTGCTCATTGCAACCTCCACCTCCCAGGT CTCTGTCACCCAGGCTAGAGTACAATGGCACAGTCTCTGCTCATTGCAACCTCCACCTCCCAGGT T C AC022400.7,NDST2 Ensembl:ENSG00000272916,Ensembl:ENSG00000166507 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs753670574 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_330465,RMVar_hsa_circ_367352,RMVar_hsa_circ_144389,RMVar_hsa_circ_89928 22517 RMVar_ID_22517 Human_SNP_ID_437794250 A-to-I Human chr10 - 73805483 73805483 73805483 TTGAGACAGAATCTCGCTCTGTCACCCAGGCTAGAGTACAATGGCACAATCTCTGCTCATTGCAA TTGAGACAGAATCTCGCTCTGTCACCCAGGCTGGAGTACAATGGCACAATCTCTGCTCATTGCAA T C AC022400.7,NDST2 Ensembl:ENSG00000272916,Ensembl:ENSG00000166507 Protein coding,Protein coding intron,intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1289723169 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_330465,RMVar_hsa_circ_367352,RMVar_hsa_circ_144389,RMVar_hsa_circ_89928 22518 RMVar_ID_22518 Human_SNP_ID_437794255 A-to-I Human chr10 - 73805505 73805505 73805505 TTTTGTTGTTGTTGTTGTTGTTTTGAGACAGAATCTCGCTCTGTCACCCAGGCTAGAGTACAATG TTTTGTTGTTGTTGTTGTTGTTTTGAGACAGAGTCTCGCTCTGTCACCCAGGCTAGAGTACAATG T C AC022400.7,NDST2 Ensembl:ENSG00000272916,Ensembl:ENSG00000166507 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs560486531 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_330465,RMVar_hsa_circ_367352,RMVar_hsa_circ_144389,RMVar_hsa_circ_89928 22519 RMVar_ID_22519 Human_SNP_ID_437822475 A-to-I Human chr10 - 73916109 73916109 73916109 CTCCTGATTAGCTGGGATTACAGGCAGGCACCACCACACCTGGCTAATTTTTTTTTGCATTTTTA CTCCTGATTAGCTGGGATTACAGGCAGGCACCGCCACACCTGGCTAATTTTTTTTTGCATTTTTA T C C10orf55 Ensembl:ENSG00000222047 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs530343972 Functional Loss SNV dbSNP153 33..33 33 - - - 22520 RMVar_ID_22520 Human_SNP_ID_437845768 A-to-I Human chr10 + 74010983 74010983 74010983 CCTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGCGAAACCCCATCTCTACTAAAAATTC CCTGAGGTCAGGAGTTCGAGACCAGCCTGGCCCACATGGCGAAACCCCATCTCTACTAAAAATTC A C AL596247.1,VCL Ensembl:ENSG00000225761,Ensembl:ENSG00000035403 lincRNA,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs368059248 Functional Loss SNV dbSNP153 33..33 33 - - - 22521 RMVar_ID_22521 Human_SNP_ID_437845777 A-to-I Human chr10 + 74010999 74010999 74010999 CGAGACCAGCCTGGCCAACATGGCGAAACCCCATCTCTACTAAAAATTCAAAAAATTGGCTGGGC CGAGACCAGCCTGGCCAACATGGCGAAACCCCGTCTCTACTAAAAATTCAAAAAATTGGCTGGGC A G AL596247.1,VCL Ensembl:ENSG00000225761,Ensembl:ENSG00000035403 lincRNA,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1347943770 Functional Loss SNV dbSNP153 33..33 33 - - - 22522 RMVar_ID_22522 Human_SNP_ID_437845784 A-to-I Human chr10 + 74011018 74011018 74011018 ATGGCGAAACCCCATCTCTACTAAAAATTCAAAAAATTGGCTGGGCATGGTGGCAGGTGCCTGTA ATGGCGAAACCCCATCTCTACTAAAAATTCAACAAATTGGCTGGGCATGGTGGCAGGTGCCTGTA A C AL596247.1,VCL Ensembl:ENSG00000225761,Ensembl:ENSG00000035403 lincRNA,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1048666524 Functional Loss SNV dbSNP153 33..33 33 - - - 22523 RMVar_ID_22523 Human_SNP_ID_437849126 A-to-I Human chr10 + 74025201 74025201 74025201 ACCATGCCTGGCTAATTTTTTGTATTTTCAGTAGAGACGGGGATTCACCATGTTGGCCTGGCTGG ACCATGCCTGGCTAATTTTTTGTATTTTCAGTGGAGACGGGGATTCACCATGTTGGCCTGGCTGG A G AL596247.1,VCL Ensembl:ENSG00000225761,Ensembl:ENSG00000035403 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs989495116 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8245986,Human_RBP_ID_11426969 RMVar_hsa_circ_334590 22524 RMVar_ID_22524 Human_SNP_ID_437849127 A-to-I Human chr10 + 74025201 74025201 74025201 ACCATGCCTGGCTAATTTTTTGTATTTTCAGTAGAGACGGGGATTCACCATGTTGGCCTGGCTGG ACCATGCCTGGCTAATTTTTTGTATTTTCAGTTGAGACGGGGATTCACCATGTTGGCCTGGCTGG A T AL596247.1,VCL Ensembl:ENSG00000225761,Ensembl:ENSG00000035403 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs989495116 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8245986,Human_RBP_ID_11426969 RMVar_hsa_circ_334590 22525 RMVar_ID_22525 Human_SNP_ID_437849817 A-to-I Human chr10 + 74028209 74028209 74028209 GTGATTCTCCTGGATCACCCTCCCAAGTAGCTAGGACTACAGGCAAGAGCCACCACACCTAGTTA GTGATTCTCCTGGATCACCCTCCCAAGTAGCTCGGACTACAGGCAAGAGCCACCACACCTAGTTA A C VCL Ensembl:ENSG00000035403 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991244559 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_334590 22526 RMVar_ID_22526 Human_SNP_ID_437862593 A-to-I Human chr10 + 74087714 74087714 74087714 AGAGGCTAGATAGGCTGGGTGTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGC AGAGGCTAGATAGGCTGGGTGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGC A G VCL Ensembl:ENSG00000035403 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1013348425 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37155,RMVar_hsa_circ_39033,RMVar_hsa_circ_318940,RMVar_hsa_circ_336702,RMVar_hsa_circ_299084,RMVar_hsa_circ_94922,RMVar_hsa_circ_35196,RMVar_hsa_circ_144406,RMVar_hsa_circ_144405,RMVar_hsa_circ_144411,RMVar_hsa_circ_51471,RMVar_hsa_circ_144410,RMVar_hsa_circ_347156,RMVar_hsa_circ_45536 22527 RMVar_ID_22527 Human_SNP_ID_437863390 A-to-I Human chr10 + 74091021 74091021 74091021 CGGGGTGTTGCTATGTTGTCAGGGCTGGTCTCAAACTCAAGGGCTCAAGCTATCCTCCCACTTCA CGGGGTGTTGCTATGTTGTCAGGGCTGGTCTCTAACTCAAGGGCTCAAGCTATCCTCCCACTTCA A T VCL Ensembl:ENSG00000035403 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1357977627 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37155,RMVar_hsa_circ_39033,RMVar_hsa_circ_336702,RMVar_hsa_circ_299084,RMVar_hsa_circ_35196,RMVar_hsa_circ_144405,RMVar_hsa_circ_51471,RMVar_hsa_circ_347156,RMVar_hsa_circ_144412,RMVar_hsa_circ_310867,RMVar_hsa_circ_274773 22528 RMVar_ID_22528 Human_SNP_ID_437865714 A-to-I Human chr10 + 74101411 74101411 74101411 GTGAGGCTGAGGTGGGAGGATTATTTGAGCCCAGAAGGTTGAGGCTGCAGTAAGCTTTGATTGCC GTGAGGCTGAGGTGGGAGGATTATTTGAGCCCGGAAGGTTGAGGCTGCAGTAAGCTTTGATTGCC A G VCL Ensembl:ENSG00000035403 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs986504263 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39033,RMVar_hsa_circ_35196,RMVar_hsa_circ_51471,RMVar_hsa_circ_15566,RMVar_hsa_circ_34602,RMVar_hsa_circ_125523,RMVar_hsa_circ_144414,RMVar_hsa_circ_52858 22529 RMVar_ID_22529 Human_SNP_ID_437866688 A-to-I Human chr10 + 74105308 74105308 74105308 CCTCTGATGAATTGAGCAAAACCATCTCCCCGATGGTGATGGATGCAAAAGCTGTGGCTGGAAAC CCTCTGATGAATTGAGCAAAACCATCTCCCCGGTGGTGATGGATGCAAAAGCTGTGGCTGGAAAC A G VCL Ensembl:ENSG00000035403 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs774388320 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22432081,Human_RBP_ID_22752458,Human_RBP_ID_23206471,Human_RBP_ID_26396807 Human_Splice_Rec_1148215,Human_Splice_Rec_1148253,Human_Splice_Rec_1148295,Human_Splice_Rec_1148343,Human_Splice_Rec_1148357 RMVar_hsa_circ_39033,RMVar_hsa_circ_35196,RMVar_hsa_circ_51471,RMVar_hsa_circ_566,RMVar_hsa_circ_15566,RMVar_hsa_circ_34602,RMVar_hsa_circ_52858,RMVar_hsa_circ_21536 22530 RMVar_ID_22530 Human_SNP_ID_437871902 A-to-I Human chr10 - 74128013 74128013 74128013 TTACTGCAACCTCCACCTCCAGGGTTCAAGTGATTCTCCTGCCTCGGCCTCCCAAGTAGCTGGGA TTACTGCAACCTCCACCTCCAGGGTTCAAGTGTTTCTCCTGCCTCGGCCTCCCAAGTAGCTGGGA T A AP3M1 Ensembl:ENSG00000185009 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1195600531 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47293,RMVar_hsa_circ_144417 22531 RMVar_ID_22531 Human_SNP_ID_437872067 A-to-I Human chr10 - 74128511 74128511 74128511 TGAGGGGCCGGGTGCAGTGGTTCACTCCTGTAATCCCAACACTTTGGGAGGCCAATGTGGGCAGA TGAGGGGCCGGGTGCAGTGGTTCACTCCTGTAGTCCCAACACTTTGGGAGGCCAATGTGGGCAGA T C AP3M1 Ensembl:ENSG00000185009 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1417667037 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47293,RMVar_hsa_circ_144417 22532 RMVar_ID_22532 Human_SNP_ID_437872113 A-to-I Human chr10 - 74128719 74128714 74128719 CTGAAAGCTGAGTACTTTGCAAGCAGAGCAAAACGGACCATGCATAACCTGGGCAAAACCATGAA CTGAAAGCTGAGTACTTTGCAAGCAGAGCAAA_____CCATGCATAACCTGGGCAAAACCATGAA GTCCGT G AP3M1 Ensembl:ENSG00000185009 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1429367974 Functional Loss DEL dbSNP153 33..37 33 - - - RMVar_hsa_circ_47293,RMVar_hsa_circ_144417 22533 RMVar_ID_22533 Human_SNP_ID_437872572 A-to-I Human chr10 - 74130642 74130642 74130642 GCCCAGAAGTTTGAGACCAGCCTGGGCAACATAACAAGACCCTGTCTCTACAAAAAAAATACAAA GCCCAGAAGTTTGAGACCAGCCTGGGCAACATGACAAGACCCTGTCTCTACAAAAAAAATACAAA T C AP3M1 Ensembl:ENSG00000185009 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs879361994 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_431,RMVar_hsa_circ_47293,RMVar_hsa_circ_144417,RMVar_hsa_circ_319622,RMVar_hsa_circ_371802,RMVar_hsa_circ_144418 22534 RMVar_ID_22534 Human_SNP_ID_437872630 A-to-I Human chr10 - 74130928 74130928 74130928 TTTTGTATTTTTAGTAGAAACGGGGTTTTGCCATGTTGCCCAGGCTGGTCCCAAACTCCTGAGCT TTTTGTATTTTTAGTAGAAACGGGGTTTTGCCGTGTTGCCCAGGCTGGTCCCAAACTCCTGAGCT T C AP3M1 Ensembl:ENSG00000185009 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11000883 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_431,RMVar_hsa_circ_47293,RMVar_hsa_circ_144417,RMVar_hsa_circ_319622,RMVar_hsa_circ_371802,RMVar_hsa_circ_144418 22535 RMVar_ID_22535 Human_SNP_ID_437872844 A-to-I Human chr10 - 74131821 74131821 74131821 ATAATAGATTTTTGCCAGGCACGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTTAGGC ATAATAGATTTTTGCCAGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTTAGGC T C AP3M1 Ensembl:ENSG00000185009 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1413535793 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_431,RMVar_hsa_circ_47293,RMVar_hsa_circ_144417,RMVar_hsa_circ_319622,RMVar_hsa_circ_371802,RMVar_hsa_circ_144418 22536 RMVar_ID_22536 Human_SNP_ID_437873203 A-to-I Human chr10 - 74133311 74133311 74133311 CAGCTCACCGCAACCTCCGCCTCCCGGGTTCAAGCAGTTCTTCTGCCTCAGCCTCCCGAGTACCT CAGCTCACCGCAACCTCCGCCTCCCGGGTTCAGGCAGTTCTTCTGCCTCAGCCTCCCGAGTACCT T C AP3M1 Ensembl:ENSG00000185009 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs918798170 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_431,RMVar_hsa_circ_47293,RMVar_hsa_circ_144417,RMVar_hsa_circ_319622,RMVar_hsa_circ_371802,RMVar_hsa_circ_144418 22537 RMVar_ID_22537 Human_SNP_ID_437873280 A-to-I Human chr10 - 74133547 74133547 74133547 TTTATTTATTTATTTATTTGAGACGGGGTCTCACACTGTTGTCCAGGCTGGAGTGCAATCACATG TTTATTTATTTATTTATTTGAGACGGGGTCTCGCACTGTTGTCCAGGCTGGAGTGCAATCACATG T C AP3M1 Ensembl:ENSG00000185009 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs755883166 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_431,RMVar_hsa_circ_47293,RMVar_hsa_circ_144417,RMVar_hsa_circ_319622,RMVar_hsa_circ_371802,RMVar_hsa_circ_144418 22538 RMVar_ID_22538 Human_SNP_ID_437873345 A-to-I Human chr10 - 74133731 74133731 74133731 AAAATTGCTTGAACCCAGGAGGCAGAGGTTGCAATGAGACAAGATCATGCCATTGCACTCCAGCC AAAATTGCTTGAACCCAGGAGGCAGAGGTTGCGATGAGACAAGATCATGCCATTGCACTCCAGCC T C AP3M1 Ensembl:ENSG00000185009 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10824079 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_431,RMVar_hsa_circ_47293,RMVar_hsa_circ_144417,RMVar_hsa_circ_319622,RMVar_hsa_circ_371802,RMVar_hsa_circ_144418 22539 RMVar_ID_22539 Human_SNP_ID_437897001 A-to-I Human chr10 + 74231675 74231675 74231675 TTTTGTTGAGATGGGGTCTTGCCATGTTGTCCAGGCTGGTCTTGAGCTCCTGGGCTCAAGTGATA TTTTGTTGAGATGGGGTCTTGCCATGTTGTCCGGGCTGGTCTTGAGCTCCTGGGCTCAAGTGATA A G ADK Ensembl:ENSG00000156110 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1246163399 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6398,RMVar_hsa_circ_89295,RMVar_hsa_circ_316501,RMVar_hsa_circ_348285,RMVar_hsa_circ_124476,RMVar_hsa_circ_144421,RMVar_hsa_circ_144422,RMVar_hsa_circ_55084 22540 RMVar_ID_22540 Human_SNP_ID_437905961 A-to-I Human chr10 + 74272415 74272415 74272415 CTCCCACCTCAGCTTCCTGAGTGTTTGGGACTACAGGCGCGCACTACCATGCCGGGTTAACTTTT CTCCCACCTCAGCTTCCTGAGTGTTTGGGACTGCAGGCGCGCACTACCATGCCGGGTTAACTTTT A G ADK Ensembl:ENSG00000156110 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1268494792 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6398,RMVar_hsa_circ_316501,RMVar_hsa_circ_348285,RMVar_hsa_circ_124476,RMVar_hsa_circ_144422,RMVar_hsa_circ_55084 22541 RMVar_ID_22541 Human_SNP_ID_437913383 A-to-I Human chr10 + 74302336 74302336 74302336 TAGAGATGGGGTTTCACCATGTTCCCTGGGCTAGTTTCAAACTCCTGAGCTCAGGCAATCAGCCC TAGAGATGGGGTTTCACCATGTTCCCTGGGCTGGTTTCAAACTCCTGAGCTCAGGCAATCAGCCC A G ADK Ensembl:ENSG00000156110 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1209122329 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6398,RMVar_hsa_circ_316501,RMVar_hsa_circ_348285,RMVar_hsa_circ_124476,RMVar_hsa_circ_144422,RMVar_hsa_circ_55084 22542 RMVar_ID_22542 Human_SNP_ID_437918557 A-to-I Human chr10 + 74325881 74325881 74325881 GTGCTGGCTTTTTTTTTTCTTTTTTAAGACAGAGTCTCTCTCTGTCACCCAGGCTGAGGTGCAGA GTGCTGGCTTTTTTTTTTCTTTTTTAAGACAGTGTCTCTCTCTGTCACCCAGGCTGAGGTGCAGA A T ADK Ensembl:ENSG00000156110 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1011847076 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11429309 RMVar_hsa_circ_348285,RMVar_hsa_circ_124476,RMVar_hsa_circ_144422,RMVar_hsa_circ_55084,RMVar_hsa_circ_60984,RMVar_hsa_circ_282801,RMVar_hsa_circ_352531,RMVar_hsa_circ_79561,RMVar_hsa_circ_144426,RMVar_hsa_circ_46815,RMVar_hsa_circ_144425 22543 RMVar_ID_22543 Human_SNP_ID_437918657 A-to-I Human chr10 + 74326388 74326388 74326388 GGGAGGCTGAGGCAGAACTTCAAGAGGCCAGGAATTTGAGGTCAACCTGGACAACATAGTGAGAC GGGAGGCTGAGGCAGAACTTCAAGAGGCCAGGGATTTGAGGTCAACCTGGACAACATAGTGAGAC A G ADK Ensembl:ENSG00000156110 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909411351 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_348285,RMVar_hsa_circ_124476,RMVar_hsa_circ_144422,RMVar_hsa_circ_55084,RMVar_hsa_circ_60984,RMVar_hsa_circ_282801,RMVar_hsa_circ_352531,RMVar_hsa_circ_79561,RMVar_hsa_circ_144426,RMVar_hsa_circ_46815,RMVar_hsa_circ_144425 22544 RMVar_ID_22544 Human_SNP_ID_437925370 A-to-I Human chr10 + 74355095 74355095 74355095 TGTCTCCTCCTGTCTTGGTCTCCCAATGTGCTAGAACTACGGGCATGAGACACTGCACCTGCTCT TGTCTCCTCCTGTCTTGGTCTCCCAATGTGCTGGAACTACGGGCATGAGACACTGCACCTGCTCT A G ADK Ensembl:ENSG00000156110 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1372253373 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_348285,RMVar_hsa_circ_124476,RMVar_hsa_circ_144422,RMVar_hsa_circ_55084,RMVar_hsa_circ_60984,RMVar_hsa_circ_282801,RMVar_hsa_circ_352531,RMVar_hsa_circ_79561,RMVar_hsa_circ_144426,RMVar_hsa_circ_46815,RMVar_hsa_circ_144425 22545 RMVar_ID_22545 Human_SNP_ID_437938317 A-to-I Human chr10 + 74412343 74412343 74412343 ATTTTATTTTTGTAGAGACGAGGTCTCACCATATTGGCCAGGCTGGTCTCGAACTGCTGGGCTTA ATTTTATTTTTGTAGAGACGAGGTCTCACCATGTTGGCCAGGCTGGTCTCGAACTGCTGGGCTTA A G ADK Ensembl:ENSG00000156110 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903930925 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17559051,Human_RBP_ID_24835059 RMVar_hsa_circ_114209,RMVar_hsa_circ_124476,RMVar_hsa_circ_144422,RMVar_hsa_circ_17800,RMVar_hsa_circ_60984,RMVar_hsa_circ_352531,RMVar_hsa_circ_79561,RMVar_hsa_circ_144426,RMVar_hsa_circ_46815,RMVar_hsa_circ_302319,RMVar_hsa_circ_369920,RMVar_hsa_circ_144428,RMVar_hsa_circ_144429,RMVar_hsa_circ_117185,RMVar_hsa_circ_144430,RMVar_hsa_circ_144431 22546 RMVar_ID_22546 Human_SNP_ID_437950867 A-to-I Human chr10 + 74469377 74469377 74469377 AAAATATTTTTTAACCTTTTAATTTATTTTTTAGAGATAGGGTCTCACTGTGTCACCCAGAACTG AAAATATTTTTTAACCTTTTAATTTATTTTTTGGAGATAGGGTCTCACTGTGTCACCCAGAACTG A G ADK Ensembl:ENSG00000156110 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1475262586 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17559054 RMVar_hsa_circ_114209,RMVar_hsa_circ_124476,RMVar_hsa_circ_144422,RMVar_hsa_circ_17800,RMVar_hsa_circ_60984,RMVar_hsa_circ_352531,RMVar_hsa_circ_79561,RMVar_hsa_circ_144426,RMVar_hsa_circ_46815,RMVar_hsa_circ_302319,RMVar_hsa_circ_369920,RMVar_hsa_circ_144428,RMVar_hsa_circ_144429,RMVar_hsa_circ_117185,RMVar_hsa_circ_144430,RMVar_hsa_circ_144431,RMVar_hsa_circ_144432,RMVar_hsa_circ_114006 22547 RMVar_ID_22547 Human_SNP_ID_437952332 A-to-I Human chr10 + 74475027 74475027 74475027 CGCACCTGTAATCCCAGCTACTTGGGAGGCTGAAGCAGGAGAATCGCTTGAACCCGGGAGGCAGA CGCACCTGTAATCCCAGCTACTTGGGAGGCTGCAGCAGGAGAATCGCTTGAACCCGGGAGGCAGA A C ADK Ensembl:ENSG00000156110 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs567105633 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2742598 RMVar_hsa_circ_114209,RMVar_hsa_circ_124476,RMVar_hsa_circ_144422,RMVar_hsa_circ_17800,RMVar_hsa_circ_60984,RMVar_hsa_circ_352531,RMVar_hsa_circ_79561,RMVar_hsa_circ_144426,RMVar_hsa_circ_46815,RMVar_hsa_circ_302319,RMVar_hsa_circ_369920,RMVar_hsa_circ_144428,RMVar_hsa_circ_144429,RMVar_hsa_circ_117185,RMVar_hsa_circ_144430,RMVar_hsa_circ_144431,RMVar_hsa_circ_144432,RMVar_hsa_circ_114006 22548 RMVar_ID_22548 Human_SNP_ID_437964983 A-to-I Human chr10 + 74531634 74531634 74531634 TGTCTCACTGCAAGCTCAAACTCCTGGGTTCAAATGATCCTCCTACCTCAACCTCCCGAGAAGCT TGTCTCACTGCAAGCTCAAACTCCTGGGTTCAGATGATCCTCCTACCTCAACCTCCCGAGAAGCT A G ADK Ensembl:ENSG00000156110 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1260114002 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17559058 RMVar_hsa_circ_114209,RMVar_hsa_circ_60984,RMVar_hsa_circ_352531,RMVar_hsa_circ_79561,RMVar_hsa_circ_144426,RMVar_hsa_circ_302319,RMVar_hsa_circ_369920,RMVar_hsa_circ_144428,RMVar_hsa_circ_144429,RMVar_hsa_circ_117185,RMVar_hsa_circ_54609,RMVar_hsa_circ_144430,RMVar_hsa_circ_144431,RMVar_hsa_circ_293061,RMVar_hsa_circ_144433 22549 RMVar_ID_22549 Human_SNP_ID_437965001 A-to-I Human chr10 + 74531717 74531717 74531717 CACCACAGCTGGCTAATTTTTAATTTTTGTAGAGAGGAGGTCTCGTTTTGTTGCCCAGGCTGGTT CACCACAGCTGGCTAATTTTTAATTTTTGTAGTGAGGAGGTCTCGTTTTGTTGCCCAGGCTGGTT A T ADK Ensembl:ENSG00000156110 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs377674403 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17559059 RMVar_hsa_circ_114209,RMVar_hsa_circ_60984,RMVar_hsa_circ_352531,RMVar_hsa_circ_79561,RMVar_hsa_circ_144426,RMVar_hsa_circ_302319,RMVar_hsa_circ_369920,RMVar_hsa_circ_144428,RMVar_hsa_circ_144429,RMVar_hsa_circ_117185,RMVar_hsa_circ_54609,RMVar_hsa_circ_144430,RMVar_hsa_circ_144431,RMVar_hsa_circ_293061,RMVar_hsa_circ_144433 22550 RMVar_ID_22550 Human_SNP_ID_437966080 A-to-I Human chr10 + 74536571 74536571 74536571 ATCAGTGGCATTAAGTACATTTGCAATGTTGTACAGCCATCACCACTATTCCTCTCCAGAACTTT ATCAGTGGCATTAAGTACATTTGCAATGTTGTGCAGCCATCACCACTATTCCTCTCCAGAACTTT A G ADK Ensembl:ENSG00000156110 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973687882 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114209,RMVar_hsa_circ_60984,RMVar_hsa_circ_352531,RMVar_hsa_circ_79561,RMVar_hsa_circ_144426,RMVar_hsa_circ_302319,RMVar_hsa_circ_369920,RMVar_hsa_circ_144428,RMVar_hsa_circ_144429,RMVar_hsa_circ_117185,RMVar_hsa_circ_54609,RMVar_hsa_circ_144430,RMVar_hsa_circ_144431,RMVar_hsa_circ_293061,RMVar_hsa_circ_144433 22551 RMVar_ID_22551 Human_SNP_ID_437966131 A-to-I Human chr10 + 74536789 74536789 74536789 CAAAAGTTGTCTGACTTAATTTCACTTAGCATAATCTTTTTAAACTTCATCCATGTTATAGCATG CAAAAGTTGTCTGACTTAATTTCACTTAGCATCATCTTTTTAAACTTCATCCATGTTATAGCATG A C ADK Ensembl:ENSG00000156110 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs375654559 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6001746,Human_RBP_ID_11430825 RMVar_hsa_circ_114209,RMVar_hsa_circ_60984,RMVar_hsa_circ_352531,RMVar_hsa_circ_79561,RMVar_hsa_circ_144426,RMVar_hsa_circ_302319,RMVar_hsa_circ_369920,RMVar_hsa_circ_144428,RMVar_hsa_circ_144429,RMVar_hsa_circ_117185,RMVar_hsa_circ_54609,RMVar_hsa_circ_144430,RMVar_hsa_circ_144431,RMVar_hsa_circ_293061,RMVar_hsa_circ_144433 22552 RMVar_ID_22552 Human_SNP_ID_437966132 A-to-I Human chr10 + 74536789 74536789 74536789 CAAAAGTTGTCTGACTTAATTTCACTTAGCATAATCTTTTTAAACTTCATCCATGTTATAGCATG CAAAAGTTGTCTGACTTAATTTCACTTAGCATGATCTTTTTAAACTTCATCCATGTTATAGCATG A G ADK Ensembl:ENSG00000156110 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs375654559 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6001746,Human_RBP_ID_11430825 RMVar_hsa_circ_114209,RMVar_hsa_circ_60984,RMVar_hsa_circ_352531,RMVar_hsa_circ_79561,RMVar_hsa_circ_144426,RMVar_hsa_circ_302319,RMVar_hsa_circ_369920,RMVar_hsa_circ_144428,RMVar_hsa_circ_144429,RMVar_hsa_circ_117185,RMVar_hsa_circ_54609,RMVar_hsa_circ_144430,RMVar_hsa_circ_144431,RMVar_hsa_circ_293061,RMVar_hsa_circ_144433 22553 RMVar_ID_22553 Human_SNP_ID_437966134 A-to-I Human chr10 + 74536799 74536799 74536799 CTGACTTAATTTCACTTAGCATAATCTTTTTAAACTTCATCCATGTTATAGCATGTTATCAGAAT CTGACTTAATTTCACTTAGCATAATCTTTTTATACTTCATCCATGTTATAGCATGTTATCAGAAT A T ADK Ensembl:ENSG00000156110 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1461983389 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6001746,Human_RBP_ID_11430825,Human_RBP_ID_17782816,Human_RBP_ID_26599859 RMVar_hsa_circ_114209,RMVar_hsa_circ_60984,RMVar_hsa_circ_352531,RMVar_hsa_circ_79561,RMVar_hsa_circ_144426,RMVar_hsa_circ_302319,RMVar_hsa_circ_369920,RMVar_hsa_circ_144428,RMVar_hsa_circ_144429,RMVar_hsa_circ_117185,RMVar_hsa_circ_54609,RMVar_hsa_circ_144430,RMVar_hsa_circ_144431,RMVar_hsa_circ_293061,RMVar_hsa_circ_144433 22554 RMVar_ID_22554 Human_SNP_ID_437966161 A-to-I Human chr10 + 74536912 74536907 74536912 TGTTTTTTGCTTCATTTTGTTGATAGACATTTAATTTGTTTCCACCTTTGATTATTATGAACAAT TGTTTTTTGCTTCATTTTGTTGATAGAC_____ATTTGTTTCCACCTTTGATTATTATGAACAAT CATTTA C ADK Ensembl:ENSG00000156110 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1448140043 Functional Loss DEL dbSNP153 29..33 33 - - - Human_RBP_ID_1771006,Human_RBP_ID_6001747 RMVar_hsa_circ_114209,RMVar_hsa_circ_60984,RMVar_hsa_circ_352531,RMVar_hsa_circ_79561,RMVar_hsa_circ_144426,RMVar_hsa_circ_302319,RMVar_hsa_circ_369920,RMVar_hsa_circ_144428,RMVar_hsa_circ_144429,RMVar_hsa_circ_117185,RMVar_hsa_circ_54609,RMVar_hsa_circ_144430,RMVar_hsa_circ_144431,RMVar_hsa_circ_293061,RMVar_hsa_circ_144433 22555 RMVar_ID_22555 Human_SNP_ID_437967161 A-to-I Human chr10 + 74541682 74541682 74541682 AGGCATGATGGCACATTCCTGTAGTCCCAACTACTTGGGAGGCTGAGGCAGGAGGATTGCTTGAG AGGCATGATGGCACATTCCTGTAGTCCCAACTGCTTGGGAGGCTGAGGCAGGAGGATTGCTTGAG A G ADK Ensembl:ENSG00000156110 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1340319263 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114209,RMVar_hsa_circ_60984,RMVar_hsa_circ_352531,RMVar_hsa_circ_79561,RMVar_hsa_circ_144426,RMVar_hsa_circ_302319,RMVar_hsa_circ_369920,RMVar_hsa_circ_144428,RMVar_hsa_circ_144429,RMVar_hsa_circ_117185,RMVar_hsa_circ_54609,RMVar_hsa_circ_144430,RMVar_hsa_circ_144431,RMVar_hsa_circ_293061,RMVar_hsa_circ_144433 22556 RMVar_ID_22556 Human_SNP_ID_437979878 A-to-I Human chr10 + 74595369 74595369 74595369 AGATTTCAAAATGACTTTGAGAAATGAAAAATACCTTTTTTTTTTTTTTTTTTTTTGGGGAGGGG AGATTTCAAAATGACTTTGAGAAATGAAAAATTCCTTTTTTTTTTTTTTTTTTTTTGGGGAGGGG A T ADK Ensembl:ENSG00000156110 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1369646603 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6001923 RMVar_hsa_circ_60984,RMVar_hsa_circ_352531,RMVar_hsa_circ_302319,RMVar_hsa_circ_144429,RMVar_hsa_circ_117185,RMVar_hsa_circ_54609,RMVar_hsa_circ_144430,RMVar_hsa_circ_293061,RMVar_hsa_circ_144434,RMVar_hsa_circ_322278,RMVar_hsa_circ_279423 22557 RMVar_ID_22557 Human_SNP_ID_437985065 A-to-I Human chr10 + 74617675 74617675 74617675 TGGAGTGCAGTGGTGCTCTCCAGGCTCACTGCAGCCTCCACCTCCTGGGCTCAAGCAGTCCTCCC TGGAGTGCAGTGGTGCTCTCCAGGCTCACTGCGGCCTCCACCTCCTGGGCTCAAGCAGTCCTCCC A G ADK Ensembl:ENSG00000156110 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1029334808 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60984,RMVar_hsa_circ_54609,RMVar_hsa_circ_322278,RMVar_hsa_circ_335266 22558 RMVar_ID_22558 Human_SNP_ID_437988835 A-to-I Human chr10 + 74634851 74634851 74634851 CCTATAGTCCCAGCTACTTGGTAGGGTGAGGCAGGAGAATCACTAGAACCTGGGAGGTAGAGGTT CCTATAGTCCCAGCTACTTGGTAGGGTGAGGCGGGAGAATCACTAGAACCTGGGAGGTAGAGGTT A G ADK Ensembl:ENSG00000156110 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049723502 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60984,RMVar_hsa_circ_54609,RMVar_hsa_circ_322278,RMVar_hsa_circ_335266 22559 RMVar_ID_22559 Human_SNP_ID_437996575 A-to-I Human chr10 + 74670224 74670224 74670224 TCACTGCTTTTGCTGTCTTGGATCAAGACCAGAAAGAAATTATTGATACCAATGGAGCTGGAGAT TCACTGCTTTTGCTGTCTTGGATCAAGACCAGGAAGAAATTATTGATACCAATGGAGCTGGAGAT A G ADK Ensembl:ENSG00000156110 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs760279818 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22432085 Human_Splice_Rec_1148414,Human_Splice_Rec_1148415,Human_Splice_Rec_1148434,Human_Splice_Rec_1148435,Human_Splice_Rec_1148454,Human_Splice_Rec_1148455,Human_Splice_Rec_1148480,Human_Splice_Rec_1148481,Human_Splice_Rec_1148502,Human_Splice_Rec_1148503,Human_Splice_Rec_1148522,Human_Splice_Rec_1148523,Human_Splice_Rec_1148544,Human_Splice_Rec_1148545,Human_Splice_Rec_1148566,Human_Splice_Rec_1148567,Human_Splice_Rec_1148584,Human_Splice_Rec_1148585,Human_Splice_Rec_1148604,Human_Splice_Rec_1148605 RMVar_hsa_circ_60984,RMVar_hsa_circ_54609,RMVar_hsa_circ_322278,RMVar_hsa_circ_335266 22560 RMVar_ID_22560 Human_SNP_ID_437997869 A-to-I Human chr10 + 74676364 74676364 74676364 GTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCCACCTGCCTCAGCCTCCCAAAGTGC GTTGGCCAGGCTGGTCTCGAACTCCTGACCTCGGGTGATCCACCTGCCTCAGCCTCCCAAAGTGC A G ADK Ensembl:ENSG00000156110 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1177337956 Functional Loss SNV dbSNP153 33..33 33 - - - 22561 RMVar_ID_22561 Human_SNP_ID_437997936 A-to-I Human chr10 + 74676693 74676693 74676693 GTTACCCAGTCTGGTCTTAAACTCTTGGCCTCAAGCAGTCCTCCTGCCTAGGACTCCCAAAGTGC GTTACCCAGTCTGGTCTTAAACTCTTGGCCTCCAGCAGTCCTCCTGCCTAGGACTCCCAAAGTGC A C ADK Ensembl:ENSG00000156110 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1168988010 Functional Loss SNV dbSNP153 33..33 33 - - - 22562 RMVar_ID_22562 Human_SNP_ID_438003837 A-to-I Human chr10 + 74702702 74702702 74702702 CTCACTGTGACCTCTGCCTCCTGAGTTCAAGCAGTTCTCCTGCCTCAGCCTCCCAAGTAGCTGGG CTCACTGTGACCTCTGCCTCCTGAGTTCAAGCGGTTCTCCTGCCTCAGCCTCCCAAGTAGCTGGG A G ADK Ensembl:ENSG00000156110 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs960038623 Functional Loss SNV dbSNP153 33..33 33 - - - 22563 RMVar_ID_22563 Human_SNP_ID_438005304 A-to-I Human chr10 + 74709767 74709767 74709767 TAATTCCACCACTTTGGGATGAGGCAGGTATCACTAGAGGTCAAGAGTTCAAGACCAGCCTGGCC TAATTCCACCACTTTGGGATGAGGCAGGTATCGCTAGAGGTCAAGAGTTCAAGACCAGCCTGGCC A G ADK Ensembl:ENSG00000156110 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1423192819 Functional Loss SNV dbSNP153 33..33 33 - - - 22564 RMVar_ID_22564 Human_SNP_ID_438043636 A-to-I Human chr10 + 74870123 74870123 74870123 GCAACTTAGCGAGACCCCACCTCTACAAAAATACAAAAATTAGACAGGTGTGATGGCATGCCCCT GCAACTTAGCGAGACCCCACCTCTACAAAAATCCAAAAATTAGACAGGTGTGATGGCATGCCCCT A C KAT6B Ensembl:ENSG00000156650 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1564532283 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96753,RMVar_hsa_circ_13937,RMVar_hsa_circ_35730,RMVar_hsa_circ_144439,RMVar_hsa_circ_144441,RMVar_hsa_circ_125164 22565 RMVar_ID_22565 Human_SNP_ID_438043645 A-to-I Human chr10 + 74870158 74870158 74870158 AAAATTAGACAGGTGTGATGGCATGCCCCTGTAGTCCCAGCGACTTGGGGGTGCTGAGGCAGGAG AAAATTAGACAGGTGTGATGGCATGCCCCTGTGGTCCCAGCGACTTGGGGGTGCTGAGGCAGGAG A G KAT6B Ensembl:ENSG00000156650 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs529342688 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96753,RMVar_hsa_circ_13937,RMVar_hsa_circ_35730,RMVar_hsa_circ_144439,RMVar_hsa_circ_144441,RMVar_hsa_circ_125164 22566 RMVar_ID_22566 Human_SNP_ID_438044273 A-to-I Human chr10 + 74872700 74872700 74872700 ACTCCTGGCTAATTAATTTTTTTTTTTTTTGTAGAGAGGGGGTTCTGCTATGTTGCCCAGGCTGG ACTCCTGGCTAATTAATTTTTTTTTTTTTTGTTGAGAGGGGGTTCTGCTATGTTGCCCAGGCTGG A T KAT6B Ensembl:ENSG00000156650 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1217844732 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96753,RMVar_hsa_circ_13937,RMVar_hsa_circ_35730,RMVar_hsa_circ_144439,RMVar_hsa_circ_144441,RMVar_hsa_circ_125164 22567 RMVar_ID_22567 Human_SNP_ID_438044949 A-to-I Human chr10 + 74875681 74875681 74875681 AGAGATGAGGTTTCACCATGCCGGCCAGGCTGATCTCGAACTCCTGAGCTCAAGTGACCTGCCCA AGAGATGAGGTTTCACCATGCCGGCCAGGCTGTTCTCGAACTCCTGAGCTCAAGTGACCTGCCCA A T KAT6B Ensembl:ENSG00000156650 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1396351136 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6002357,Human_RBP_ID_11431947 RMVar_hsa_circ_96753,RMVar_hsa_circ_13937,RMVar_hsa_circ_35730,RMVar_hsa_circ_144439,RMVar_hsa_circ_144441,RMVar_hsa_circ_125164 22568 RMVar_ID_22568 Human_SNP_ID_438045875 A-to-I Human chr10 + 74879833 74879833 74879833 AAAGGTAGATCTGGCCAGGCATGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAAGC AAAGGTAGATCTGGCCAGGCATGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAAGC A G KAT6B Ensembl:ENSG00000156650 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1485544594 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96753,RMVar_hsa_circ_13937,RMVar_hsa_circ_35730,RMVar_hsa_circ_144439,RMVar_hsa_circ_144441,RMVar_hsa_circ_125164 22569 RMVar_ID_22569 Human_SNP_ID_438051196 A-to-I Human chr10 + 74904288 74904288 74904288 AGTCCAGGCACAGGTAACTGGGTCCCCTGCTCAAGGACTCACCAGGCTGAAATCAAAATGTCAGC AGTCCAGGCACAGGTAACTGGGTCCCCTGCTCGAGGACTCACCAGGCTGAAATCAAAATGTCAGC A G KAT6B Ensembl:ENSG00000156650 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1206830747 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96753,RMVar_hsa_circ_13937,RMVar_hsa_circ_35730,RMVar_hsa_circ_144439,RMVar_hsa_circ_144441,RMVar_hsa_circ_125164 22570 RMVar_ID_22570 Human_SNP_ID_608789224 A-to-I Human chr16 + 75030920 75030920 75030920 TGGAGTGCGGTGGCGTGATTTCGGTTCACTGCAACCTCCGCCTCCCGGGTTCAAGCAATTCTTCC TGGAGTGCGGTGGCGTGATTTCGGTTCACTGCTACCTCCGCCTCCCGGGTTCAAGCAATTCTTCC A T ZNRF1 Ensembl:ENSG00000186187 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs980925219 Functional Loss SNV dbSNP153 33..33 33 - - - 22571 RMVar_ID_22571 Human_SNP_ID_608789834 A-to-I Human chr16 + 75032765 75032765 75032765 TTACAAAGGACCAGATGCAGTAGCTCATGCCTATAATACCAGCACTTTGGGAGGCCAAGTCAGGA TTACAAAGGACCAGATGCAGTAGCTCATGCCTGTAATACCAGCACTTTGGGAGGCCAAGTCAGGA A G ZNRF1 Ensembl:ENSG00000186187 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs561518040 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12814130,Human_RBP_ID_17565171 22572 RMVar_ID_22572 Human_SNP_ID_608795826 A-to-I Human chr16 + 75052189 75052189 75052189 GGGAGGCCAAGGCTGGAGGATTGCTTGAACCCAGAAGTTCGAGACCAACTTGGGCAACATGGTGA GGGAGGCCAAGGCTGGAGGATTGCTTGAACCCGGAAGTTCGAGACCAACTTGGGCAACATGGTGA A G ZNRF1 Ensembl:ENSG00000186187 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1285199472 Functional Loss SNV dbSNP153 33..33 33 - - - 22573 RMVar_ID_22573 Human_SNP_ID_608795828 A-to-I Human chr16 + 75052191 75052191 75052191 GAGGCCAAGGCTGGAGGATTGCTTGAACCCAGAAGTTCGAGACCAACTTGGGCAACATGGTGAAA GAGGCCAAGGCTGGAGGATTGCTTGAACCCAGGAGTTCGAGACCAACTTGGGCAACATGGTGAAA A G ZNRF1 Ensembl:ENSG00000186187 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs774786476 Functional Loss SNV dbSNP153 33..33 33 - - - 22574 RMVar_ID_22574 Human_SNP_ID_608795859 A-to-I Human chr16 + 75052310 75052310 75052310 GTAGTCTCAGCTGCTTGGGAGGCTGAGGTGGGAAAATTGCTTGAGCCCAGGAGGCAGAGGTTGCA GTAGTCTCAGCTGCTTGGGAGGCTGAGGTGGGGAAATTGCTTGAGCCCAGGAGGCAGAGGTTGCA A G ZNRF1 Ensembl:ENSG00000186187 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1384845943 Functional Loss SNV dbSNP153 33..33 33 - - - 22575 RMVar_ID_22575 Human_SNP_ID_608795865 A-to-I Human chr16 + 75052326 75052326 75052326 GGGAGGCTGAGGTGGGAAAATTGCTTGAGCCCAGGAGGCAGAGGTTGCAGTGAGCCAGCATGGCA GGGAGGCTGAGGTGGGAAAATTGCTTGAGCCCGGGAGGCAGAGGTTGCAGTGAGCCAGCATGGCA A G ZNRF1 Ensembl:ENSG00000186187 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1172107038 Functional Loss SNV dbSNP153 33..33 33 - - - 22576 RMVar_ID_22576 Human_SNP_ID_608796176 A-to-I Human chr16 + 75053482 75053481 75053483 CTGGTGGCACACGCCTATAGTCCCAGCTACTCAAGAGACTGAGGCAGGAGAATCGCTTGAACCTG CTGGTGGCACACGCCTATAGTCCCAGCTACTC__GAGACTGAGGCAGGAGAATCGCTTGAACCTG CAA C ZNRF1 Ensembl:ENSG00000186187 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1199833034 Functional Loss DEL dbSNP153 33..34 33 - - - 22577 RMVar_ID_22577 Human_SNP_ID_608796177 A-to-I Human chr16 + 75053482 75053482 75053482 CTGGTGGCACACGCCTATAGTCCCAGCTACTCAAGAGACTGAGGCAGGAGAATCGCTTGAACCTG CTGGTGGCACACGCCTATAGTCCCAGCTACTCGAGAGACTGAGGCAGGAGAATCGCTTGAACCTG A G ZNRF1 Ensembl:ENSG00000186187 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1192249978 Functional Loss SNV dbSNP153 33..33 33 - - - 22578 RMVar_ID_22578 Human_SNP_ID_608868804 A-to-I Human chr16 - 75257547 75257547 75257547 AAGAGGCTGAGGTGGGAGGATCGTTTGAGCCCAGGAGGTTGAGGCTGCAGTGAGCTGTGACTGTG AAGAGGCTGAGGTGGGAGGATCGTTTGAGCCCGGGAGGTTGAGGCTGCAGTGAGCTGTGACTGTG T C BCAR1 Ensembl:ENSG00000050820 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1320785108 Functional Loss SNV dbSNP153 33..33 33 - - - 22579 RMVar_ID_22579 Human_SNP_ID_608881804 A-to-I Human chr16 - 75300350 75300350 75300350 CCGGGAGGCGGAGGTTGCAATGAGCCAAGATCATGCTGTTGCACTCCAGCCTAGGCAACAAGAGC CCGGGAGGCGGAGGTTGCAATGAGCCAAGATCGTGCTGTTGCACTCCAGCCTAGGCAACAAGAGC T C CFDP1 Ensembl:ENSG00000153774 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042557311 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108998,RMVar_hsa_circ_180060,RMVar_hsa_circ_180059 22580 RMVar_ID_22580 Human_SNP_ID_608899998 A-to-I Human chr16 - 75361064 75361064 75361064 TGGAGGTTGTAGTAAGCCAAGATCACGCCACTACACTCCAGCCTGGGCCATAGAGTAAGACCCTG TGGAGGTTGTAGTAAGCCAAGATCACGCCACTGCACTCCAGCCTGGGCCATAGAGTAAGACCCTG T C CFDP1 Ensembl:ENSG00000153774 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs775514478 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17564330 RMVar_hsa_circ_108998,RMVar_hsa_circ_180059 22581 RMVar_ID_22581 Human_SNP_ID_608900800 A-to-I Human chr16 - 75363651 75363651 75363651 TGGCTCACACCTGTAATCGCAGCACTTTGGGAAGCCAAGGTGGGTGGCTCATTTGAGGTCAGGTG TGGCTCACACCTGTAATCGCAGCACTTTGGGATGCCAAGGTGGGTGGCTCATTTGAGGTCAGGTG T A CFDP1 Ensembl:ENSG00000153774 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048072158 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108998,RMVar_hsa_circ_180059,RMVar_hsa_circ_180061 22582 RMVar_ID_22582 Human_SNP_ID_608902370 A-to-I Human chr16 - 75368789 75368789 75368789 CTCTACAAAAAATGCACAGATTAGCTGGGCGTAGTGGCACGTGCCTGTAGTACTCAGAATGCTGA CTCTACAAAAAATGCACAGATTAGCTGGGCGTGGTGGCACGTGCCTGTAGTACTCAGAATGCTGA T C CFDP1 Ensembl:ENSG00000153774 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1317783495 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12816096 RMVar_hsa_circ_108998,RMVar_hsa_circ_180059,RMVar_hsa_circ_180061 22583 RMVar_ID_22583 Human_SNP_ID_608902715 A-to-I Human chr16 - 75369887 75369887 75369887 GAGCTTGGTGGTGCAGGCCTGTAGTTCCAGCCACTGGGGAGGCTGTGGCATGAGAATCGCTTGAA GAGCTTGGTGGTGCAGGCCTGTAGTTCCAGCCGCTGGGGAGGCTGTGGCATGAGAATCGCTTGAA T C CFDP1 Ensembl:ENSG00000153774 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444094755 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25230190 RMVar_hsa_circ_108998,RMVar_hsa_circ_180059,RMVar_hsa_circ_180061 22584 RMVar_ID_22584 Human_SNP_ID_608902998 A-to-I Human chr16 - 75370854 75370854 75370854 TTTTTTTAATTCTTTTTTTAAATTTTTGAGACAGTCTTGCTCTGTCACCCAGGCTGGAGTGCAGT TTTTTTTAATTCTTTTTTTAAATTTTTGAGACTGTCTTGCTCTGTCACCCAGGCTGGAGTGCAGT T A CFDP1 Ensembl:ENSG00000153774 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs538348779 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108998,RMVar_hsa_circ_180059,RMVar_hsa_circ_180061 22585 RMVar_ID_22585 Human_SNP_ID_608909309 A-to-I Human chr16 - 75392626 75392626 75392626 GGGCTTGGTGGCACATGCCCTTAATCCCAGCTACCTAGGAGGCTGAGGCAGCAGAATCGCTTGAA GGGCTTGGTGGCACATGCCCTTAATCCCAGCTTCCTAGGAGGCTGAGGCAGCAGAATCGCTTGAA T A CFDP1 Ensembl:ENSG00000153774 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs927722815 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17564332 RMVar_hsa_circ_108998,RMVar_hsa_circ_180062,RMVar_hsa_circ_180059,RMVar_hsa_circ_180061,RMVar_hsa_circ_180063,RMVar_hsa_circ_180064 22586 RMVar_ID_22586 Human_SNP_ID_608909837 A-to-I Human chr16 - 75393992 75393992 75393992 GCAGTGCAGTGGCGCAATCTCGGCTCACTGCAAGCTCCGCCTCCCGGGTTCATGTCATTCTTCTG GCAGTGCAGTGGCGCAATCTCGGCTCACTGCATGCTCCGCCTCCCGGGTTCATGTCATTCTTCTG T A CFDP1 Ensembl:ENSG00000153774 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1030734433 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108998,RMVar_hsa_circ_180062,RMVar_hsa_circ_180059,RMVar_hsa_circ_180061,RMVar_hsa_circ_180063,RMVar_hsa_circ_180064 22587 RMVar_ID_22587 Human_SNP_ID_608909838 A-to-I Human chr16 - 75393992 75393992 75393992 GCAGTGCAGTGGCGCAATCTCGGCTCACTGCAAGCTCCGCCTCCCGGGTTCATGTCATTCTTCTG GCAGTGCAGTGGCGCAATCTCGGCTCACTGCACGCTCCGCCTCCCGGGTTCATGTCATTCTTCTG T G CFDP1 Ensembl:ENSG00000153774 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1030734433 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108998,RMVar_hsa_circ_180062,RMVar_hsa_circ_180059,RMVar_hsa_circ_180061,RMVar_hsa_circ_180063,RMVar_hsa_circ_180064 22588 RMVar_ID_22588 Human_SNP_ID_608914692 A-to-I Human chr16 - 75408739 75408739 75408739 ACAGGGTCTTGATCTGTTGCCGAGGCTAGAGTACAGTGGCATGATCTCGGCTCTCTGCAACCTCC ACAGGGTCTTGATCTGTTGCCGAGGCTAGAGTGCAGTGGCATGATCTCGGCTCTCTGCAACCTCC T C CFDP1 Ensembl:ENSG00000153774 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1311952380 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2157,RMVar_hsa_circ_108998,RMVar_hsa_circ_180059,RMVar_hsa_circ_180063,RMVar_hsa_circ_274868,RMVar_hsa_circ_62140,RMVar_hsa_circ_180066 22589 RMVar_ID_22589 Human_SNP_ID_608914694 A-to-I Human chr16 - 75408744 75408744 75408744 TTGAGACAGGGTCTTGATCTGTTGCCGAGGCTAGAGTACAGTGGCATGATCTCGGCTCTCTGCAA TTGAGACAGGGTCTTGATCTGTTGCCGAGGCTGGAGTACAGTGGCATGATCTCGGCTCTCTGCAA T C CFDP1 Ensembl:ENSG00000153774 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569151026 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2157,RMVar_hsa_circ_108998,RMVar_hsa_circ_180059,RMVar_hsa_circ_180063,RMVar_hsa_circ_274868,RMVar_hsa_circ_62140,RMVar_hsa_circ_180066 22590 RMVar_ID_22590 Human_SNP_ID_608914699 A-to-I Human chr16 - 75408769 75408767 75408769 ACTATTTTTTTTTATTATTATTATTTTGAGACAGGGTCTTGATCTGTTGCCGAGGCTAGAGTACA ACTATTTTTTTTTATTATTATTATTTTGAGAC__GGTCTTGATCTGTTGCCGAGGCTAGAGTACA CCT C CFDP1 Ensembl:ENSG00000153774 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388657075 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_2157,RMVar_hsa_circ_108998,RMVar_hsa_circ_180059,RMVar_hsa_circ_180063,RMVar_hsa_circ_274868,RMVar_hsa_circ_62140,RMVar_hsa_circ_180066 22591 RMVar_ID_22591 Human_SNP_ID_608914701 A-to-I Human chr16 - 75408769 75408769 75408769 ACTATTTTTTTTTATTATTATTATTTTGAGACAGGGTCTTGATCTGTTGCCGAGGCTAGAGTACA ACTATTTTTTTTTATTATTATTATTTTGAGACCGGGTCTTGATCTGTTGCCGAGGCTAGAGTACA T G CFDP1 Ensembl:ENSG00000153774 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913321194 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2157,RMVar_hsa_circ_108998,RMVar_hsa_circ_180059,RMVar_hsa_circ_180063,RMVar_hsa_circ_274868,RMVar_hsa_circ_62140,RMVar_hsa_circ_180066 22592 RMVar_ID_22592 Human_SNP_ID_608922339 A-to-I Human chr16 - 75430556 75430556 75430556 GGGAGGCTGAGGCACGAGATCTCTTGAACCCAAGAGGTGGGGGTTGCAGTGAGTGAAGATCATGC GGGAGGCTGAGGCACGAGATCTCTTGAACCCAGGAGGTGGGGGTTGCAGTGAGTGAAGATCATGC T C AC009163.5,CFDP1 Ensembl:ENSG00000261717,Ensembl:ENSG00000153774 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1021635801 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12817145 RMVar_hsa_circ_108998,RMVar_hsa_circ_180059 22593 RMVar_ID_22593 Human_SNP_ID_608927004 A-to-I Human chr16 - 75443832 75443832 75443832 CACCCGCCTCGGCCTCCCAACGTGATGGGACTATAGACATGAGCCATCATGCTTGGCCTTCTTGA CACCCGCCTCGGCCTCCCAACGTGATGGGACTGTAGACATGAGCCATCATGCTTGGCCTTCTTGA T C AC009163.5,TMEM170A Ensembl:ENSG00000261717,Ensembl:ENSG00000166822 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037422492 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_479661,Human_RBP_ID_9836799,Human_RBP_ID_12817209 22594 RMVar_ID_22594 Human_SNP_ID_608927032 A-to-I Human chr16 - 75443906 75443906 75443906 TTTTGTATTTTTAGTAGAGACAGGGTTTGATTATGTTGGACAGGCTGGTCTCAAACTCCTGACTT TTTTGTATTTTTAGTAGAGACAGGGTTTGATTTTGTTGGACAGGCTGGTCTCAAACTCCTGACTT T A AC009163.5,TMEM170A Ensembl:ENSG00000261717,Ensembl:ENSG00000166822 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1184040341 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4384468,Human_RBP_ID_8810435,Human_RBP_ID_12817216 22595 RMVar_ID_22595 Human_SNP_ID_608927049 A-to-I Human chr16 - 75443973 75443973 75443973 AGTGATTGTCCTGCCTTGGCCGCTGAGTAGCTAGGATTACTGGCACCCGCCACAAGGCCCAGCTA AGTGATTGTCCTGCCTTGGCCGCTGAGTAGCTGGGATTACTGGCACCCGCCACAAGGCCCAGCTA T C AC009163.5,TMEM170A Ensembl:ENSG00000261717,Ensembl:ENSG00000166822 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs530981296 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_479662,Human_RBP_ID_6538282,Human_RBP_ID_12817222,Human_RBP_ID_17881224 22596 RMVar_ID_22596 Human_SNP_ID_608927482 A-to-I Human chr16 - 75445352 75445352 75445352 TGAGCCGAGACCACGCCACTGAACTCCAGCTTAGGCCACAGGGCAAGACCCTGTCTTAAAATAAT TGAGCCGAGACCACGCCACTGAACTCCAGCTTGGGCCACAGGGCAAGACCCTGTCTTAAAATAAT T C AC009163.5,TMEM170A Ensembl:ENSG00000261717,Ensembl:ENSG00000166822 Protein coding,Protein coding intron,3'UTR GSE38233;GSE112787;GSE107867;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;293 Flip-In T-REx cells,empty vector;ASD brains,cerebellum;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29967493,30559470,32596459 RNA-Seq:(High) rs1346670479 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_479676,Human_RBP_ID_4384488 22597 RMVar_ID_22597 Human_SNP_ID_608927508 A-to-I Human chr16 - 75445412 75445412 75445412 TCAGCTACCCAAGAGGCTAAAGTGGGAGGATCACTTGTGCCTGGGAGGTTCAGGCTGCTGTGAGC TCAGCTACCCAAGAGGCTAAAGTGGGAGGATCGCTTGTGCCTGGGAGGTTCAGGCTGCTGTGAGC T C AC009163.5,TMEM170A Ensembl:ENSG00000261717,Ensembl:ENSG00000166822 Protein coding,Protein coding intron,3'UTR GSE112787;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 293 Flip-In T-REx cells,empty vector;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29967493,32596459,32596459 RNA-Seq:(High) rs910247915 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4384489 22598 RMVar_ID_22598 Human_SNP_ID_608927548 A-to-I Human chr16 - 75445523 75445522 75445524 GGAGGTCGATGTGGGAGGATTGCTTGAGCCCAAGAGTTCAAGACTGGCCTGGGCAACATAGTGAG GGAGGTCGATGTGGGAGGATTGCTTGAGCCC__GAGTTCAAGACTGGCCTGGGCAACATAGTGAG CTT C AC009163.5,TMEM170A Ensembl:ENSG00000261717,Ensembl:ENSG00000166822 Protein coding,Protein coding intron,3'UTR GSE38233;GSE99789;GSE112787;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,EC109;293 Flip-In T-REx cells,empty vector;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29796672,29967493,32596459,32596459 RNA-Seq:(High) rs1474822962 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_12817254 22599 RMVar_ID_22599 Human_SNP_ID_608927564 A-to-I Human chr16 - 75445570 75445570 75445570 ACTTATGGCTGGGCGCAGTGGCTCACACCTATAATCCCAGCACTTTGGGAGGTCGATGTGGGAGG ACTTATGGCTGGGCGCAGTGGCTCACACCTATTATCCCAGCACTTTGGGAGGTCGATGTGGGAGG T A AC009163.5,TMEM170A Ensembl:ENSG00000261717,Ensembl:ENSG00000166822 Protein coding,Protein coding intron,3'UTR GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1415863145 Functional Loss SNV dbSNP153 33..33 33 - - - 22600 RMVar_ID_22600 Human_SNP_ID_608927685 A-to-I Human chr16 - 75445993 75445993 75445993 TTTTTGTATTTTTAGTAGAGATAGGTTTCACCATCTTGCCCAGGCTGGTCTTGAACTCCTGACCT TTTTTGTATTTTTAGTAGAGATAGGTTTCACCGTCTTGCCCAGGCTGGTCTTGAACTCCTGACCT T C AC009163.5,TMEM170A Ensembl:ENSG00000261717,Ensembl:ENSG00000166822 Protein coding,Protein coding intron,3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1133757 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1461887 22601 RMVar_ID_22601 Human_SNP_ID_608928479 A-to-I Human chr16 - 75448874 75448874 75448874 TATTTTTTGTAAAGACAAGGTTTGGTCATGTTACCCAGGATGGTCTCAAACTCCTGGGCTCAAGC TATTTTTTGTAAAGACAAGGTTTGGTCATGTTTCCCAGGATGGTCTCAAACTCCTGGGCTCAAGC T A AC009163.5,TMEM170A Ensembl:ENSG00000261717,Ensembl:ENSG00000166822 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1019736001 Functional Loss SNV dbSNP153 33..33 33 - - - 22602 RMVar_ID_22602 Human_SNP_ID_608928486 A-to-I Human chr16 - 75448895 75448895 75448895 ACTACACCCAGCTAATTTTTGTATTTTTTGTAAAGACAAGGTTTGGTCATGTTACCCAGGATGGT ACTACACCCAGCTAATTTTTGTATTTTTTGTATAGACAAGGTTTGGTCATGTTACCCAGGATGGT T A AC009163.5,TMEM170A Ensembl:ENSG00000261717,Ensembl:ENSG00000166822 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1405614273 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12817346 22603 RMVar_ID_22603 Human_SNP_ID_608928516 A-to-I Human chr16 - 75449015 75449015 75449015 GTTCTGTCACCCAGGCTGGAGTGCAGTGGCATAGTCACAGCTCACTGCAGCCTTGACCTCCCTAG GTTCTGTCACCCAGGCTGGAGTGCAGTGGCATGGTCACAGCTCACTGCAGCCTTGACCTCCCTAG T C AC009163.5,TMEM170A Ensembl:ENSG00000261717,Ensembl:ENSG00000166822 Protein coding,Protein coding intron,intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs542977245 Functional Loss SNV dbSNP153 33..33 33 - - - 22604 RMVar_ID_22604 Human_SNP_ID_608928630 A-to-I Human chr16 - 75449370 75449370 75449370 GGAGCCATGATCATGCCACCGCATTCCAGCCTAGGTGAAAGAGTGAGACACTGTCTCAAAAAAAA GGAGCCATGATCATGCCACCGCATTCCAGCCTGGGTGAAAGAGTGAGACACTGTCTCAAAAAAAA T C AC009163.5,TMEM170A Ensembl:ENSG00000261717,Ensembl:ENSG00000166822 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1458925882 Functional Loss SNV dbSNP153 33..33 33 - - - 22605 RMVar_ID_22605 Human_SNP_ID_608928648 A-to-I Human chr16 - 75449430 75449430 75449430 TGTGCCTGTAGTCCCAGCTGCTCGGGAGGATCACTTGAGCCCAGGAGGTTGAGGCTGCAGGGAGC TGTGCCTGTAGTCCCAGCTGCTCGGGAGGATCGCTTGAGCCCAGGAGGTTGAGGCTGCAGGGAGC T C AC009163.5,TMEM170A Ensembl:ENSG00000261717,Ensembl:ENSG00000166822 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1257386725 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12817350 22606 RMVar_ID_22606 Human_SNP_ID_608928666 A-to-I Human chr16 - 75449475 75449475 75449475 GTCTCTACAAAAAATAAATAAATAAAATAGCCAGGTGTGGTGGCGTGTGCCTGTAGTCCCAGCTG GTCTCTACAAAAAATAAATAAATAAAATAGCCGGGTGTGGTGGCGTGTGCCTGTAGTCCCAGCTG T C AC009163.5,TMEM170A Ensembl:ENSG00000261717,Ensembl:ENSG00000166822 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs779510006 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12817352 22607 RMVar_ID_22607 Human_SNP_ID_608928684 A-to-I Human chr16 - 75449518 75449518 75449518 GTCCAAGAGTTCAAAACCAGCCTTGGCAACATAGTGAGACCCTGTCTCTACAAAAAATAAATAAA GTCCAAGAGTTCAAAACCAGCCTTGGCAACATGGTGAGACCCTGTCTCTACAAAAAATAAATAAA T C AC009163.5,TMEM170A Ensembl:ENSG00000261717,Ensembl:ENSG00000166822 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs753452268 Functional Loss SNV dbSNP153 33..33 33 - - - 22608 RMVar_ID_22608 Human_SNP_ID_608929111 A-to-I Human chr16 - 75450957 75450957 75450957 AAGACAAATTTTGATGACAAGAATTCTTTGCCAGGTGTAGTGGCTCATGACTGTAATCCCAGCAC AAGACAAATTTTGATGACAAGAATTCTTTGCCGGGTGTAGTGGCTCATGACTGTAATCCCAGCAC T C AC009163.5,TMEM170A Ensembl:ENSG00000261717,Ensembl:ENSG00000166822 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1246820452 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12817372,Human_RBP_ID_17564336 22609 RMVar_ID_22609 Human_SNP_ID_608929253 A-to-I Human chr16 - 75451440 75451440 75451440 GGCTCAAGTAATCCTCCTCCATCAGCCTCCCAAGAAGCTTGGACTACAGGGGTGTGCCACCATGC GGCTCAAGTAATCCTCCTCCATCAGCCTCCCAGGAAGCTTGGACTACAGGGGTGTGCCACCATGC T C AC009163.5,TMEM170A Ensembl:ENSG00000261717,Ensembl:ENSG00000166822 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031719526 Functional Loss SNV dbSNP153 33..33 33 - - - 22610 RMVar_ID_22610 Human_SNP_ID_608929260 A-to-I Human chr16 - 75451462 75451462 75451462 TCACTGCAGCCTCCACCTCTTGGGCTCAAGTAATCCTCCTCCATCAGCCTCCCAAGAAGCTTGGA TCACTGCAGCCTCCACCTCTTGGGCTCAAGTAGTCCTCCTCCATCAGCCTCCCAAGAAGCTTGGA T C AC009163.5,TMEM170A Ensembl:ENSG00000261717,Ensembl:ENSG00000166822 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs183982616 Functional Loss SNV dbSNP153 33..33 33 - - - 22611 RMVar_ID_22611 Human_SNP_ID_608936568 A-to-I Human chr16 - 75473955 75473955 75473955 GTCGATCAGGCTGGGCTGGAACTCCTGACCTCAGGTGATCCACCTGCCTTGGCCTCCCAATGTGC GTCGATCAGGCTGGGCTGGAACTCCTGACCTCGGGTGATCCACCTGCCTTGGCCTCCCAATGTGC T C CHST6 Ensembl:ENSG00000183196 Protein coding 3'UTR GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1046653049 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80364,RMVar_hsa_circ_180069,RMVar_hsa_circ_180070 22612 RMVar_ID_22612 Human_SNP_ID_608936569 A-to-I Human chr16 - 75473955 75473955 75473955 GTCGATCAGGCTGGGCTGGAACTCCTGACCTCAGGTGATCCACCTGCCTTGGCCTCCCAATGTGC GTCGATCAGGCTGGGCTGGAACTCCTGACCTCCGGTGATCCACCTGCCTTGGCCTCCCAATGTGC T G CHST6 Ensembl:ENSG00000183196 Protein coding 3'UTR GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1046653049 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80364,RMVar_hsa_circ_180069,RMVar_hsa_circ_180070 22613 RMVar_ID_22613 Human_SNP_ID_608937127 A-to-I Human chr16 - 75475983 75475983 75475983 AAATTAGCCGGGTGTGGTGGTGCACACCTGTAATTCCAGCTACTCAGGAGGCTGAGGCAGGAGAA AAATTAGCCGGGTGTGGTGGTGCACACCTGTAGTTCCAGCTACTCAGGAGGCTGAGGCAGGAGAA T C CHST6 Ensembl:ENSG00000183196 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1324927754 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80364,RMVar_hsa_circ_180069,RMVar_hsa_circ_180070 22614 RMVar_ID_22614 Human_SNP_ID_608972263 A-to-I Human chr16 - 75589890 75589890 75589890 AGGCATGTGCCACCATGCCCGGCTAATTTTGTATTTTTAGTAGAGATGGGGTTTCTCCATGAAGG AGGCATGTGCCACCATGCCCGGCTAATTTTGTGTTTTTAGTAGAGATGGGGTTTCTCCATGAAGG T C AC025287.1 Ensembl:ENSG00000259992 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs529647330 Functional Loss SNV dbSNP153 33..33 33 - - - 22615 RMVar_ID_22615 Human_SNP_ID_608972945 A-to-I Human chr16 - 75592333 75592333 75592333 TAAAAATTAGCCGGGCGTAGTGGTGCATGCCTATAATCCCAGCTACTCGGGAGGCTGTCAGGAGA TAAAAATTAGCCGGGCGTAGTGGTGCATGCCTGTAATCCCAGCTACTCGGGAGGCTGTCAGGAGA T C AC025287.1 Ensembl:ENSG00000259992 lincRNA intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs765107491 Functional Loss SNV dbSNP153 33..33 33 - - - 22616 RMVar_ID_22616 Human_SNP_ID_608973094 A-to-I Human chr16 - 75592891 75592891 75592891 AAAAATAGAGACGGGGTCTCACTATGATGGCCAGATTGGTCTTTAATTCCTGGCCTCAAACGATC AAAAATAGAGACGGGGTCTCACTATGATGGCCTGATTGGTCTTTAATTCCTGGCCTCAAACGATC T A AC025287.1 Ensembl:ENSG00000259992 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978689761 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23165610 22617 RMVar_ID_22617 Human_SNP_ID_608973356 A-to-I Human chr16 - 75593709 75593709 75593709 GTCTCGAATGCTTGAGCTCAAATGATCTTCCCACCTTGGCCTTCCATAGTGCTGGGATTACAGGC GTCTCGAATGCTTGAGCTCAAATGATCTTCCCGCCTTGGCCTTCCATAGTGCTGGGATTACAGGC T C AC025287.1 Ensembl:ENSG00000259992 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1237273444 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12818064 22618 RMVar_ID_22618 Human_SNP_ID_608974180 A-to-I Human chr16 - 75596532 75596532 75596532 TATTTTTTGTAGAGACGGGGTTTCACCGTGTTAACCAGGATTGTCTCGATCTCCTGACCTTGTGA TATTTTTTGTAGAGACGGGGTTTCACCGTGTTGACCAGGATTGTCTCGATCTCCTGACCTTGTGA T C AC025287.1 Ensembl:ENSG00000259992 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1369788549 Functional Loss SNV dbSNP153 33..33 33 - - - 22619 RMVar_ID_22619 Human_SNP_ID_608974238 A-to-I Human chr16 - 75596667 75596667 75596667 CTCTGTTGCCCAGGCTGGAGTACAGTGGCACAATCTTGGCTCACTGCAAGCTCTGGATTCACGCC CTCTGTTGCCCAGGCTGGAGTACAGTGGCACAGTCTTGGCTCACTGCAAGCTCTGGATTCACGCC T C AC025287.1 Ensembl:ENSG00000259992 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1246354169 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5184134 22620 RMVar_ID_22620 Human_SNP_ID_608974242 A-to-I Human chr16 - 75596678 75596678 75596678 ATGGAGTCTTGCTCTGTTGCCCAGGCTGGAGTACAGTGGCACAATCTTGGCTCACTGCAAGCTCT ATGGAGTCTTGCTCTGTTGCCCAGGCTGGAGTGCAGTGGCACAATCTTGGCTCACTGCAAGCTCT T C AC025287.1 Ensembl:ENSG00000259992 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1177400781 Functional Loss SNV dbSNP153 33..33 33 - - - 22621 RMVar_ID_22621 Human_SNP_ID_608974729 A-to-I Human chr16 - 75598175 75598175 75598175 CTACTCAGGAGGCTGAGGCAGAAGAATCTCTCAAACCCAGGAGGTGGAGGTTGCAGTGAGCCAGG CTACTCAGGAGGCTGAGGCAGAAGAATCTCTCGAACCCAGGAGGTGGAGGTTGCAGTGAGCCAGG T C AC025287.1,ADAT1 Ensembl:ENSG00000259992,Ensembl:ENSG00000065457 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1464734614 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3509960,Human_RBP_ID_5096787,Human_RBP_ID_12818139 22622 RMVar_ID_22622 Human_SNP_ID_608974790 A-to-I Human chr16 - 75598333 75598333 75598333 GCAGTGGCTCACGCCTGTAATCCCAACACTTTAGGAGGCCGAGGTGGGCAGATCACGACGTCAGG GCAGTGGCTCACGCCTGTAATCCCAACACTTTGGGAGGCCGAGGTGGGCAGATCACGACGTCAGG T C AC025287.1,ADAT1 Ensembl:ENSG00000259992,Ensembl:ENSG00000065457 lincRNA,Protein coding intron,intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1244860785 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3509960,Human_RBP_ID_5096787 22623 RMVar_ID_22623 Human_SNP_ID_608974941 A-to-I Human chr16 - 75598792 75598792 75598792 TTTTTAGGCCGGGCACGGTGGCTTACGCCTGTAATTCCAACACTTTGGGAGGCTGAGGCAGGCAG TTTTTAGGCCGGGCACGGTGGCTTACGCCTGTGATTCCAACACTTTGGGAGGCTGAGGCAGGCAG T C AC025287.1,ADAT1 Ensembl:ENSG00000259992,Ensembl:ENSG00000065457 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs975676165 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_762463 RMVar_hsa_circ_267048 22624 RMVar_ID_22624 Human_SNP_ID_608975084 A-to-I Human chr16 - 75599210 75599210 75599210 GGGCATGGTGGCGCACACCTGTAATCCTAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCTTGAA GGGCATGGTGGCGCACACCTGTAATCCTAGCTGCTCGGGAGGCTGAGGCAGGAGAATTGCTTGAA T C AC025287.1,ADAT1 Ensembl:ENSG00000259992,Ensembl:ENSG00000065457 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1279529677 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25230521 RMVar_hsa_circ_267048 22625 RMVar_ID_22625 Human_SNP_ID_608975088 A-to-I Human chr16 - 75599219 75599219 75599219 AAACTAGCCGGGCATGGTGGCGCACACCTGTAATCCTAGCTACTCGGGAGGCTGAGGCAGGAGAA AAACTAGCCGGGCATGGTGGCGCACACCTGTAGTCCTAGCTACTCGGGAGGCTGAGGCAGGAGAA T C AC025287.1,ADAT1 Ensembl:ENSG00000259992,Ensembl:ENSG00000065457 lincRNA,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1137875 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267048 22626 RMVar_ID_22626 Human_SNP_ID_608975089 A-to-I Human chr16 - 75599220 75599220 75599220 AAAACTAGCCGGGCATGGTGGCGCACACCTGTAATCCTAGCTACTCGGGAGGCTGAGGCAGGAGA AAAACTAGCCGGGCATGGTGGCGCACACCTGTGATCCTAGCTACTCGGGAGGCTGAGGCAGGAGA T C AC025287.1,ADAT1 Ensembl:ENSG00000259992,Ensembl:ENSG00000065457 lincRNA,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1137874 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267048 22627 RMVar_ID_22627 Human_SNP_ID_608975104 A-to-I Human chr16 - 75599259 75599259 75599259 TGGCCAACCTGGTGAAACCCTGTCTCTACTAAAAATGCAAAAACTAGCCGGGCATGGTGGCGCAC TGGCCAACCTGGTGAAACCCTGTCTCTACTAAGAATGCAAAAACTAGCCGGGCATGGTGGCGCAC T C AC025287.1,ADAT1 Ensembl:ENSG00000259992,Ensembl:ENSG00000065457 lincRNA,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1472826570 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267048 22628 RMVar_ID_22628 Human_SNP_ID_608975105 A-to-I Human chr16 - 75599261 75599261 75599261 CCTGGCCAACCTGGTGAAACCCTGTCTCTACTAAAAATGCAAAAACTAGCCGGGCATGGTGGCGC CCTGGCCAACCTGGTGAAACCCTGTCTCTACTGAAAATGCAAAAACTAGCCGGGCATGGTGGCGC T C AC025287.1,ADAT1 Ensembl:ENSG00000259992,Ensembl:ENSG00000065457 lincRNA,Protein coding intron,intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1198563521 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267048 22629 RMVar_ID_22629 Human_SNP_ID_608975122 A-to-I Human chr16 - 75599324 75599323 75599324 TAATCCCAGCACTTTGGGAAGCCCAGGCAGGCAGATCACTTGAGGTCAGGAGTTCAAGACCAGCC TAATCCCAGCACTTTGGGAAGCCCAGGCAGGC_GATCACTTGAGGTCAGGAGTTCAAGACCAGCC CT C AC025287.1,ADAT1 Ensembl:ENSG00000259992,Ensembl:ENSG00000065457 lincRNA,Protein coding intron,intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,31158229,32596459 RNA-Seq:(High) rs1414890769 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_267048 22630 RMVar_ID_22630 Human_SNP_ID_608975791 A-to-I Human chr16 - 75601682 75601682 75601682 ACAATTTCAGCTCACTGCAGCCTCCGCCTCCCAGGTTCAAGTGATTTTCCTGCCTCAGTCTCCAG ACAATTTCAGCTCACTGCAGCCTCCGCCTCCCGGGTTCAAGTGATTTTCCTGCCTCAGTCTCCAG T C AC025287.1,ADAT1 Ensembl:ENSG00000259992,Ensembl:ENSG00000065457 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs896278428 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267048,RMVar_hsa_circ_180075 22631 RMVar_ID_22631 Human_SNP_ID_608977541 A-to-I Human chr16 - 75607108 75607108 75607108 ATCTCTCTACAGCCTCGCAAGTAGCTGGGACTACAGATGCCCGCCACCACGCCCAGCTAATTTTT ATCTCTCTACAGCCTCGCAAGTAGCTGGGACTGCAGATGCCCGCCACCACGCCCAGCTAATTTTT T C AC025287.1,ADAT1 Ensembl:ENSG00000259992,Ensembl:ENSG00000065457 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1400121338 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22545,RMVar_hsa_circ_267048,RMVar_hsa_circ_323654,RMVar_hsa_circ_180075,RMVar_hsa_circ_272488,RMVar_hsa_circ_180076,RMVar_hsa_circ_180077 22632 RMVar_ID_22632 Human_SNP_ID_608989981 A-to-I Human chr16 - 75643542 75643542 75643542 ACCCCATCTTCACTAAAAATACCAAAAAAATTAGCCGGGCATGGTGGCGGGCACCTGTAGTCCCA ACCCCATCTTCACTAAAAATACCAAAAAAATTGGCCGGGCATGGTGGCGGGCACCTGTAGTCCCA T C KARS1 Ensembl:ENSG00000065427 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1171841267 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_180087,RMVar_hsa_circ_92653,RMVar_hsa_circ_180090,RMVar_hsa_circ_114972,RMVar_hsa_circ_55277 22633 RMVar_ID_22633 Human_SNP_ID_609215028 A-to-I Human chr16 + 76374952 76374952 76374952 ACTATGCCTGGCTAATTTTTGTCTTTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGG ACTATGCCTGGCTAATTTTTGTCTTTTTTAGTGGAGATGGGGTTTCACCATGTTGGCCAGGCTGG A G AC106741.2,CNTNAP4 Ensembl:ENSG00000287694,Ensembl:ENSG00000152910 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946362737 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8147,RMVar_hsa_circ_22404 22634 RMVar_ID_22634 Human_SNP_ID_609261662 A-to-I Human chr16 + 76523824 76523824 76523824 CATGGTGGCACTCGCCTGTAATCCCAGCGTTCAAGAAGCTGAGGTGGGAGGATGGTTGAACCCAG CATGGTGGCACTCGCCTGTAATCCCAGCGTTCGAGAAGCTGAGGTGGGAGGATGGTTGAACCCAG A G AC106741.2,CNTNAP4 Ensembl:ENSG00000287694,Ensembl:ENSG00000152910 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs9941180 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19292,RMVar_hsa_circ_352852 22635 RMVar_ID_22635 Human_SNP_ID_609261663 A-to-I Human chr16 + 76523824 76523824 76523824 CATGGTGGCACTCGCCTGTAATCCCAGCGTTCAAGAAGCTGAGGTGGGAGGATGGTTGAACCCAG CATGGTGGCACTCGCCTGTAATCCCAGCGTTCTAGAAGCTGAGGTGGGAGGATGGTTGAACCCAG A T AC106741.2,CNTNAP4 Ensembl:ENSG00000287694,Ensembl:ENSG00000152910 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs9941180 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19292,RMVar_hsa_circ_352852 22636 RMVar_ID_22636 Human_SNP_ID_609270923 A-to-I Human chr16 + 76554670 76554670 76554670 TTAACTTGTTCACCTTTCTTTACACTCTGAATATGATACGGATATAGAAAGTAAACAATTATTCT TTAACTTGTTCACCTTTCTTTACACTCTGAATCTGATACGGATATAGAAAGTAAACAATTATTCT A C AC106741.2,CNTNAP4 Ensembl:ENSG00000287694,Ensembl:ENSG00000152910 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs571286233 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_180115 22637 RMVar_ID_22637 Human_SNP_ID_609270925 A-to-I Human chr16 + 76554673 76554673 76554673 ACTTGTTCACCTTTCTTTACACTCTGAATATGATACGGATATAGAAAGTAAACAATTATTCTGTT ACTTGTTCACCTTTCTTTACACTCTGAATATGTTACGGATATAGAAAGTAAACAATTATTCTGTT A T AC106741.2,CNTNAP4 Ensembl:ENSG00000287694,Ensembl:ENSG00000152910 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1035417834 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_180115 22638 RMVar_ID_22638 Human_SNP_ID_609270929 A-to-I Human chr16 + 76554681 76554681 76554681 ACCTTTCTTTACACTCTGAATATGATACGGATATAGAAAGTAAACAATTATTCTGTTGCATTGCC ACCTTTCTTTACACTCTGAATATGATACGGATGTAGAAAGTAAACAATTATTCTGTTGCATTGCC A G AC106741.2,CNTNAP4 Ensembl:ENSG00000287694,Ensembl:ENSG00000152910 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1399529281 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_180115 22639 RMVar_ID_22639 Human_SNP_ID_609270933 A-to-I Human chr16 + 76554694 76554694 76554694 CTCTGAATATGATACGGATATAGAAAGTAAACAATTATTCTGTTGCATTGCCAGGGAGATACAAT CTCTGAATATGATACGGATATAGAAAGTAAACCATTATTCTGTTGCATTGCCAGGGAGATACAAT A C AC106741.2,CNTNAP4 Ensembl:ENSG00000287694,Ensembl:ENSG00000152910 Protein coding,Protein coding intron,intron GSE47997;GSE100210;GSE100210;GSE107867 K562 cells&HepG2 cells;HepG2 cell line;HepG2 cell line;ASD brains,frontal_cortex - 23474544,29129909,29129909,30559470 RNA-Seq:(High) rs1415315847 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_180115 22640 RMVar_ID_22640 Human_SNP_ID_609270939 A-to-I Human chr16 + 76554708 76554708 76554708 CGGATATAGAAAGTAAACAATTATTCTGTTGCATTGCCAGGGAGATACAATTTTAAAGTTTTTGT CGGATATAGAAAGTAAACAATTATTCTGTTGCCTTGCCAGGGAGATACAATTTTAAAGTTTTTGT A C AC106741.2,CNTNAP4 Ensembl:ENSG00000287694,Ensembl:ENSG00000152910 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1344198145 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_180115 22641 RMVar_ID_22641 Human_SNP_ID_609271049 A-to-I Human chr16 + 76555034 76555030 76555039 AAAACTTTAAAATTGTATCTCCCTGGCAGGGCAACAGGATAATTGTTTACTTTCTATATCCATAT AAAACTTTAAAATTGTATCTCCCTGGCAATGCAACAGCATAATTGTTTACTTTCTATATCCATAT GGGCAACAGG ATGCAACAGC AC106741.2,CNTNAP4 Ensembl:ENSG00000287694,Ensembl:ENSG00000152910 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs71378616 Functional Loss MNV dbSNP153 29..38 33 - - - RMVar_hsa_circ_180115 22642 RMVar_ID_22642 Human_SNP_ID_609271055 A-to-I Human chr16 + 76555034 76555034 76555034 AAAACTTTAAAATTGTATCTCCCTGGCAGGGCAACAGGATAATTGTTTACTTTCTATATCCATAT AAAACTTTAAAATTGTATCTCCCTGGCAGGGCGACAGGATAATTGTTTACTTTCTATATCCATAT A G AC106741.2,CNTNAP4 Ensembl:ENSG00000287694,Ensembl:ENSG00000152910 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs185276434 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_180115 22643 RMVar_ID_22643 Human_SNP_ID_609271065 A-to-I Human chr16 + 76555059 76555059 76555059 GCAGGGCAACAGGATAATTGTTTACTTTCTATATCCATATCATATTCAGAGTGTAAAGAAAGGTG GCAGGGCAACAGGATAATTGTTTACTTTCTATGTCCATATCATATTCAGAGTGTAAAGAAAGGTG A G AC106741.2,CNTNAP4 Ensembl:ENSG00000287694,Ensembl:ENSG00000152910 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs373388939 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_180115 22644 RMVar_ID_22644 Human_SNP_ID_609271066 A-to-I Human chr16 + 76555063 76555063 76555063 GGCAACAGGATAATTGTTTACTTTCTATATCCATATCATATTCAGAGTGTAAAGAAAGGTGAACC GGCAACAGGATAATTGTTTACTTTCTATATCCGTATCATATTCAGAGTGTAAAGAAAGGTGAACC A G AC106741.2,CNTNAP4 Ensembl:ENSG00000287694,Ensembl:ENSG00000152910 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs913389896 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_180115 22645 RMVar_ID_22645 Human_SNP_ID_609789728 A-to-I Human chr16 + 78121913 78121913 78121913 GAACTCCTGACATTAGGCAATCTGCTTGCCTCAACCTCCCCAAATGCTGGGATTACAGGTGTGAA GAACTCCTGACATTAGGCAATCTGCTTGCCTCCACCTCCCCAAATGCTGGGATTACAGGTGTGAA A C WWOX Ensembl:ENSG00000186153 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs966004169 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18684889 RMVar_hsa_circ_180131,RMVar_hsa_circ_117481,RMVar_hsa_circ_341330,RMVar_hsa_circ_180132,RMVar_hsa_circ_29910 22646 RMVar_ID_22646 Human_SNP_ID_609789735 A-to-I Human chr16 + 78121923 78121923 78121923 CATTAGGCAATCTGCTTGCCTCAACCTCCCCAAATGCTGGGATTACAGGTGTGAACCGCTGTGCC CATTAGGCAATCTGCTTGCCTCAACCTCCCCAGATGCTGGGATTACAGGTGTGAACCGCTGTGCC A G WWOX Ensembl:ENSG00000186153 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1255810862 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18684889 RMVar_hsa_circ_180131,RMVar_hsa_circ_117481,RMVar_hsa_circ_341330,RMVar_hsa_circ_180132,RMVar_hsa_circ_29910 22647 RMVar_ID_22647 Human_SNP_ID_609790066 A-to-I Human chr16 + 78122760 78122760 78122760 CTGAATAGCTGGGATTACAGGCGTGAGCCACTATGTCCGGCTAATTTTTGTATTTTTCGTAGAGA CTGAATAGCTGGGATTACAGGCGTGAGCCACTGTGTCCGGCTAATTTTTGTATTTTTCGTAGAGA A G WWOX Ensembl:ENSG00000186153 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1046552587 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_180131,RMVar_hsa_circ_117481,RMVar_hsa_circ_341330,RMVar_hsa_circ_180132,RMVar_hsa_circ_29910 22648 RMVar_ID_22648 Human_SNP_ID_609790078 A-to-I Human chr16 + 78122794 78122793 78122795 GTCCGGCTAATTTTTGTATTTTTCGTAGAGACAGGGATTCACCATGTTGGCCAAGCTGGTCTTGA GTCCGGCTAATTTTTGTATTTTTCGTAGAGAC__GGATTCACCATGTTGGCCAAGCTGGTCTTGA CAG C WWOX Ensembl:ENSG00000186153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs888608684 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_12819314 RMVar_hsa_circ_180131,RMVar_hsa_circ_117481,RMVar_hsa_circ_341330,RMVar_hsa_circ_180132,RMVar_hsa_circ_29910 22649 RMVar_ID_22649 Human_SNP_ID_609813443 A-to-I Human chr16 + 78187437 78187437 78187437 GTTCTAGACCAACATGGTGAAAACCAGTCTCTACTAAAAATACAAAAAATTAGCTGGCCGTGGTG GTTCTAGACCAACATGGTGAAAACCAGTCTCTCCTAAAAATACAAAAAATTAGCTGGCCGTGGTG A C WWOX Ensembl:ENSG00000186153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs557634601 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_180131,RMVar_hsa_circ_117481,RMVar_hsa_circ_58698 22650 RMVar_ID_22650 Human_SNP_ID_609813444 A-to-I Human chr16 + 78187437 78187437 78187437 GTTCTAGACCAACATGGTGAAAACCAGTCTCTACTAAAAATACAAAAAATTAGCTGGCCGTGGTG GTTCTAGACCAACATGGTGAAAACCAGTCTCTGCTAAAAATACAAAAAATTAGCTGGCCGTGGTG A G WWOX Ensembl:ENSG00000186153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs557634601 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_180131,RMVar_hsa_circ_117481,RMVar_hsa_circ_58698 22651 RMVar_ID_22651 Human_SNP_ID_609814359 A-to-I Human chr16 + 78189835 78189835 78189835 TGCCACCACGCTCAGCTAATTTTTGTATGTTTAGTAGAGACGAGGTTTCACCATGTTTGTCAGGT TGCCACCACGCTCAGCTAATTTTTGTATGTTTGGTAGAGACGAGGTTTCACCATGTTTGTCAGGT A G WWOX Ensembl:ENSG00000186153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs548340746 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_180131,RMVar_hsa_circ_117481,RMVar_hsa_circ_58698 22652 RMVar_ID_22652 Human_SNP_ID_609840113 A-to-I Human chr16 + 78265100 78265100 78265100 TCAGCTCACTCCAACCTCTGCCTGCCTGGTTCAAGTGATTCTCCTTCTTCAGCCTCCCAAGTTGC TCAGCTCACTCCAACCTCTGCCTGCCTGGTTCGAGTGATTCTCCTTCTTCAGCCTCCCAAGTTGC A G WWOX Ensembl:ENSG00000186153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1446917411 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_180131,RMVar_hsa_circ_117481,RMVar_hsa_circ_58698 22653 RMVar_ID_22653 Human_SNP_ID_609917120 A-to-I Human chr16 + 78442057 78442057 78442057 AGTTGAGGAGGCCAAGCTGGGAGGATGACTTGAGCCTGGGAGTTGGAGGCTGCAGTGAGCTATGA AGTTGAGGAGGCCAAGCTGGGAGGATGACTTGGGCCTGGGAGTTGGAGGCTGCAGTGAGCTATGA A G WWOX Ensembl:ENSG00000186153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1161952263 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17206376 22654 RMVar_ID_22654 Human_SNP_ID_609918843 A-to-I Human chr16 + 78445690 78445690 78445690 CTTGAGGCCGGGAGTTTGAAACCAGCCTAGCTAACACGGTGAAACCCTTCTCTACTAAAAATACA CTTGAGGCCGGGAGTTTGAAACCAGCCTAGCTGACACGGTGAAACCCTTCTCTACTAAAAATACA A G WWOX Ensembl:ENSG00000186153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs896526299 Functional Loss SNV dbSNP153 33..33 33 - - - 22655 RMVar_ID_22655 Human_SNP_ID_609921709 A-to-I Human chr16 + 78452628 78452628 78452628 CTCCCGAGTAGCTGGGACTGTAGGCATGCACTACCACACCTGGCTAATTATTATGTTTTTAATAG CTCCCGAGTAGCTGGGACTGTAGGCATGCACTGCCACACCTGGCTAATTATTATGTTTTTAATAG A G WWOX Ensembl:ENSG00000186153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1274068346 Functional Loss SNV dbSNP153 33..33 33 - - - 22656 RMVar_ID_22656 Human_SNP_ID_609922035 A-to-I Human chr16 + 78453329 78453329 78453329 CCTGTAATCCCAGCTGCTTGGGAGGCTGAGGCAGGAAAATCGTTTGAACCCGAGAGGTGGAGGTG CCTGTAATCCCAGCTGCTTGGGAGGCTGAGGCGGGAAAATCGTTTGAACCCGAGAGGTGGAGGTG A G WWOX Ensembl:ENSG00000186153 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1045874298 Functional Loss SNV dbSNP153 33..33 33 - - - 22657 RMVar_ID_22657 Human_SNP_ID_609922037 A-to-I Human chr16 + 78453334 78453334 78453334 AATCCCAGCTGCTTGGGAGGCTGAGGCAGGAAAATCGTTTGAACCCGAGAGGTGGAGGTGGCAGT AATCCCAGCTGCTTGGGAGGCTGAGGCAGGAAGATCGTTTGAACCCGAGAGGTGGAGGTGGCAGT A G WWOX Ensembl:ENSG00000186153 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs906981274 Functional Loss SNV dbSNP153 33..33 33 - - - 22658 RMVar_ID_22658 Human_SNP_ID_609922063 A-to-I Human chr16 + 78453385 78453385 78453385 GTGGAGGTGGCAGTGAGTGGAGATCACGCCACAGCACTTCAGCCTGGGCGCATGAGCGAGACTAT GTGGAGGTGGCAGTGAGTGGAGATCACGCCACCGCACTTCAGCCTGGGCGCATGAGCGAGACTAT A C WWOX Ensembl:ENSG00000186153 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1342578929 Functional Loss SNV dbSNP153 33..33 33 - - - 22659 RMVar_ID_22659 Human_SNP_ID_609923034 A-to-I Human chr16 + 78455522 78455522 78455522 AATTAGCTGGGTGTGTGGTAGTGTGTGCCTGTAGTCCCAGCTACTCTGGATGCTGAGGCACGAGA AATTAGCTGGGTGTGTGGTAGTGTGTGCCTGTTGTCCCAGCTACTCTGGATGCTGAGGCACGAGA A T WWOX Ensembl:ENSG00000186153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1238358260 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17564341 22660 RMVar_ID_22660 Human_SNP_ID_609942105 A-to-I Human chr16 + 78498778 78498778 78498778 GCAGTGGCATGATGGCATGATCATAGTTCACTATAATCTCGAACTCCTGGTTTCAAGTAGTCTTC GCAGTGGCATGATGGCATGATCATAGTTCACTGTAATCTCGAACTCCTGGTTTCAAGTAGTCTTC A G WWOX Ensembl:ENSG00000186153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1489026696 Functional Loss SNV dbSNP153 33..33 33 - - - 22661 RMVar_ID_22661 Human_SNP_ID_609942121 A-to-I Human chr16 + 78498804 78498804 78498804 TTCACTATAATCTCGAACTCCTGGTTTCAAGTAGTCTTCCTGCCTTGGCCTCCCAAAATGCTAGG TTCACTATAATCTCGAACTCCTGGTTTCAAGTGGTCTTCCTGCCTTGGCCTCCCAAAATGCTAGG A G WWOX Ensembl:ENSG00000186153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs940043175 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26638888 22662 RMVar_ID_22662 Human_SNP_ID_609955199 A-to-I Human chr16 + 78527503 78527503 78527503 TTTTGTAGAGGTGGAGTTTCGCCATGTTGGCCAGGCTGGTCTTGAATTCCTGACTTCAAGTGATG TTTTGTAGAGGTGGAGTTTCGCCATGTTGGCCTGGCTGGTCTTGAATTCCTGACTTCAAGTGATG A T WWOX Ensembl:ENSG00000186153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1000477808 Functional Loss SNV dbSNP153 33..33 33 - - - 22663 RMVar_ID_22663 Human_SNP_ID_610073732 A-to-I Human chr16 + 78769760 78769760 78769760 CACAGTGACTCATGCCTGTCTGTAATCCCAGCACTTTGGAAGGCCAAGGTGGAAGGATCGCCTGA CACAGTGACTCATGCCTGTCTGTAATCCCAGCCCTTTGGAAGGCCAAGGTGGAAGGATCGCCTGA A C WWOX Ensembl:ENSG00000186153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042003494 Functional Loss SNV dbSNP153 33..33 33 - - - 22664 RMVar_ID_22664 Human_SNP_ID_610091044 A-to-I Human chr16 + 78803564 78803564 78803564 GACCTTGTGGGCTCAAGCAGTCGTCCTGCCTCAGCCTCCCAAGTAGCTTAGAACCACAGGCATAT GACCTTGTGGGCTCAAGCAGTCGTCCTGCCTCCGCCTCCCAAGTAGCTTAGAACCACAGGCATAT A C WWOX Ensembl:ENSG00000186153 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs550979623 Functional Loss SNV dbSNP153 33..33 33 - - - 22665 RMVar_ID_22665 Human_SNP_ID_610091053 A-to-I Human chr16 + 78803572 78803572 78803572 GGGCTCAAGCAGTCGTCCTGCCTCAGCCTCCCAAGTAGCTTAGAACCACAGGCATATACCACCAT GGGCTCAAGCAGTCGTCCTGCCTCAGCCTCCCCAGTAGCTTAGAACCACAGGCATATACCACCAT A C WWOX Ensembl:ENSG00000186153 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs112544498 Functional Loss SNV dbSNP153 33..33 33 - - - 22666 RMVar_ID_22666 Human_SNP_ID_610091103 A-to-I Human chr16 + 78803679 78803679 78803679 TGTGGTCTCCCTATGTTGCCCAGGTTGCTCTCAAACTCCTAGGCTCAAGCAGTCTTCCCACCCTG TGTGGTCTCCCTATGTTGCCCAGGTTGCTCTCCAACTCCTAGGCTCAAGCAGTCTTCCCACCCTG A C WWOX Ensembl:ENSG00000186153 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1212219974 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17564367 22667 RMVar_ID_22667 Human_SNP_ID_610119766 A-to-I Human chr16 + 78861222 78861208 78861223 TTTTCCTTCTCTGTTGAAGGCCTGAATAAAATAAAAGACTGAGTAAGAAAGAATTGACTCCCTCT TTTTCCTTCTCTGTTGAAG_______________AAGACTGAGTAAGAAAGAATTGACTCCCTCT GGCCTGAATAAAATAA G WWOX Ensembl:ENSG00000186153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs927086096 Functional Loss DEL dbSNP153 20..34 33 - - - Human_RBP_ID_17564370 22668 RMVar_ID_22668 Human_SNP_ID_610142306 A-to-I Human chr16 + 78905583 78905583 78905583 TTTTATTTTTTGTAGAAATGGGGTCTCACCATATTGACCAGGCCGGACTCAAACTCCGAGATGCA TTTTATTTTTTGTAGAAATGGGGTCTCACCATGTTGACCAGGCCGGACTCAAACTCCGAGATGCA A G WWOX Ensembl:ENSG00000186153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs528050187 Functional Loss SNV dbSNP153 33..33 33 - - - 22669 RMVar_ID_22669 Human_SNP_ID_610199242 A-to-I Human chr16 + 79017242 79017242 79017242 CACGAGGTCAGAAGTTGGAGACCATCCTGGCTAACACAGTGAAACCCCATATCTCCTAAAAATAC CACGAGGTCAGAAGTTGGAGACCATCCTGGCTGACACAGTGAAACCCCATATCTCCTAAAAATAC A G WWOX,AC009145.4 Ensembl:ENSG00000186153,Ensembl:ENSG00000280274 Protein coding,Other intron,exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1157922247 Functional Loss SNV dbSNP153 33..33 33 - - - 22670 RMVar_ID_22670 Human_SNP_ID_610199248 A-to-I Human chr16 + 79017247 79017247 79017247 GGTCAGAAGTTGGAGACCATCCTGGCTAACACAGTGAAACCCCATATCTCCTAAAAATACAAAAA GGTCAGAAGTTGGAGACCATCCTGGCTAACACGGTGAAACCCCATATCTCCTAAAAATACAAAAA A G WWOX,AC009145.4 Ensembl:ENSG00000186153,Ensembl:ENSG00000280274 Protein coding,Other intron,exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs570188356 Functional Loss SNV dbSNP153 33..33 33 - - - 22671 RMVar_ID_22671 Human_SNP_ID_610461534 A-to-I Human chr16 - 79683093 79683093 79683093 TAGTCCCAGCCACTAGGGAGGCCGAGGCAGGAAAATGGCGTGAACCCAGGAGGCAGAGCTTGCAG TAGTCCCAGCCACTAGGGAGGCCGAGGCAGGAGAATGGCGTGAACCCAGGAGGCAGAGCTTGCAG T C MAFTRR RNACentral:URS0000D5A0BA lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs866955163 Functional Loss SNV dbSNP153 33..33 33 - - - 22672 RMVar_ID_22672 Human_SNP_ID_610877384 A-to-I Human chr16 - 80819145 80819145 80819145 TTTCCGGCCAGGGGCGGTGGTTCACTCCTGTAATCCCAGCATTTTGGGAGGCTGAGGCGGGCGGG TTTCCGGCCAGGGGCGGTGGTTCACTCCTGTATTCCCAGCATTTTGGGAGGCTGAGGCGGGCGGG T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1205151051 Functional Loss SNV dbSNP153 33..33 33 - - - 22673 RMVar_ID_22673 Human_SNP_ID_610906772 A-to-I Human chr16 - 80906791 80906791 80906791 ATGGTGATATATGCTTGTGGTCCCAGCTACTCAGAAGGCTGAGGTGAGAGGGTGGTTTAAGCCCA ATGGTGATATATGCTTGTGGTCCCAGCTACTCGGAAGGCTGAGGTGAGAGGGTGGTTTAAGCCCA T C AC009070.1 Ensembl:ENSG00000286221 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749183744 Functional Loss SNV dbSNP153 33..33 33 - - - 22674 RMVar_ID_22674 Human_SNP_ID_610931525 A-to-I Human chr16 - 80978892 80978892 80978892 TATTTTTAGTAGAGACGGGGCTTCACCGTGTTAGCTAGGATGGTCTTGATCTTCTGAGCTTGTTA TATTTTTAGTAGAGACGGGGCTTCACCGTGTTGGCTAGGATGGTCTTGATCTTCTGAGCTTGTTA T C CMC2,AC009070.1 Ensembl:ENSG00000103121,Ensembl:ENSG00000286221 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs925149039 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_304357 22675 RMVar_ID_22675 Human_SNP_ID_610931917 A-to-I Human chr16 - 80979815 80979815 80979815 GAGTTTGAGACCAGCCTAGCCAACATGGTGAAACCCAGCTCTACTGAAAGTACAAAAAAATTAGC GAGTTTGAGACCAGCCTAGCCAACATGGTGAATCCCAGCTCTACTGAAAGTACAAAAAAATTAGC T A CMC2,AC009070.1 Ensembl:ENSG00000103121,Ensembl:ENSG00000286221 Protein coding,Protein coding intron,intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1364606212 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_304357 22676 RMVar_ID_22676 Human_SNP_ID_610931923 A-to-I Human chr16 - 80979825 80979825 80979825 CTGAGGTCAGGAGTTTGAGACCAGCCTAGCCAACATGGTGAAACCCAGCTCTACTGAAAGTACAA CTGAGGTCAGGAGTTTGAGACCAGCCTAGCCAGCATGGTGAAACCCAGCTCTACTGAAAGTACAA T C CMC2,AC009070.1 Ensembl:ENSG00000103121,Ensembl:ENSG00000286221 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1032773265 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_304357 22677 RMVar_ID_22677 Human_SNP_ID_610932192 A-to-I Human chr16 - 80980779 80980779 80980779 GTGATCCTCCCACCTCAGCCTCCTGAGTAGCTAGGACGACAGGTGCGTACCACCATGCCTGGTTA GTGATCCTCCCACCTCAGCCTCCTGAGTAGCTGGGACGACAGGTGCGTACCACCATGCCTGGTTA T C CMC2,AC009070.1 Ensembl:ENSG00000103121,Ensembl:ENSG00000286221 Protein coding,Protein coding intron,intron GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line - 24183664,31158229 RNA-Seq:(High) rs3177094 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1743395,Human_Splice_Rec_1743401,Human_Splice_Rec_1743439,Human_Splice_Rec_1743467,Human_Splice_Rec_1743485,Human_Splice_Rec_1743493,Human_Splice_Rec_1743503 RMVar_hsa_circ_57058,RMVar_hsa_circ_304357,RMVar_hsa_circ_53081 22678 RMVar_ID_22678 Human_SNP_ID_610943305 A-to-I Human chr16 + 81014304 81014304 81014304 TCGCCCAGGCTGGAGTGCAGTAACGCCATCTCAGCTCACCGCGACCTCTGCCTCCTGGATTCAAG TCGCCCAGGCTGGAGTGCAGTAACGCCATCTCCGCTCACCGCGACCTCTGCCTCCTGGATTCAAG A C CENPN Ensembl:ENSG00000166451 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs534160304 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1743631 RMVar_hsa_circ_91153,RMVar_hsa_circ_364108,RMVar_hsa_circ_70435,RMVar_hsa_circ_180151,RMVar_hsa_circ_75072,RMVar_hsa_circ_305685,RMVar_hsa_circ_180152 22679 RMVar_ID_22679 Human_SNP_ID_610948063 A-to-I Human chr16 + 81029407 81029403 81029407 AAATTTTTTCCTTTCTAATTTTTTATTTCTTTATTTATTTATTGAGACAGGGTCTCACTGTGTCA AAATTTTTTCCTTTCTAATTTTTTATTTC____TTTATTTATTGAGACAGGGTCTCACTGTGTCA CTTTA C CENPN Ensembl:ENSG00000166451 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs971392239 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_6541118,Human_RBP_ID_20151680,Human_RBP_ID_24477034,Human_RBP_ID_26447000 Human_miRNA_ID_1950935,Human_miRNA_ID_1952221,Human_miRNA_ID_2444400 RMVar_hsa_circ_91153,RMVar_hsa_circ_180151,RMVar_hsa_circ_92162,RMVar_hsa_circ_103407,RMVar_hsa_circ_180158,RMVar_hsa_circ_180159 22680 RMVar_ID_22680 Human_SNP_ID_610948066 A-to-I Human chr16 + 81029407 81029407 81029407 AAATTTTTTCCTTTCTAATTTTTTATTTCTTTATTTATTTATTGAGACAGGGTCTCACTGTGTCA AAATTTTTTCCTTTCTAATTTTTTATTTCTTTCTTTATTTATTGAGACAGGGTCTCACTGTGTCA A C CENPN Ensembl:ENSG00000166451 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs181901938 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6541118,Human_RBP_ID_20151680,Human_RBP_ID_24477034,Human_RBP_ID_26447000 Human_miRNA_ID_1950935,Human_miRNA_ID_1952221,Human_miRNA_ID_2444400 RMVar_hsa_circ_91153,RMVar_hsa_circ_180151,RMVar_hsa_circ_92162,RMVar_hsa_circ_103407,RMVar_hsa_circ_180158,RMVar_hsa_circ_180159 22681 RMVar_ID_22681 Human_SNP_ID_610948067 A-to-I Human chr16 + 81029411 81029411 81029411 TTTTTCCTTTCTAATTTTTTATTTCTTTATTTATTTATTGAGACAGGGTCTCACTGTGTCACCCA TTTTTCCTTTCTAATTTTTTATTTCTTTATTTGTTTATTGAGACAGGGTCTCACTGTGTCACCCA A G CENPN Ensembl:ENSG00000166451 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs958938557 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6541118,Human_RBP_ID_17565185,Human_RBP_ID_20151680,Human_RBP_ID_24477034,Human_RBP_ID_26445419 Human_miRNA_ID_1950935,Human_miRNA_ID_1952221,Human_miRNA_ID_2444400 RMVar_hsa_circ_91153,RMVar_hsa_circ_180151,RMVar_hsa_circ_92162,RMVar_hsa_circ_103407,RMVar_hsa_circ_180158,RMVar_hsa_circ_180159 22682 RMVar_ID_22682 Human_SNP_ID_610948120 A-to-I Human chr16 + 81029612 81029612 81029612 TGTTTTTTGTTTTTTGAGACAAGTCTCCTTCTATCGCCCAGGCTGGAGTGCAATGGCACAATCTT TGTTTTTTGTTTTTTGAGACAAGTCTCCTTCTGTCGCCCAGGCTGGAGTGCAATGGCACAATCTT A G CENPN Ensembl:ENSG00000166451 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs147211540 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6541123,Human_RBP_ID_17564768,Human_RBP_ID_26445420 RMVar_hsa_circ_91153,RMVar_hsa_circ_180151,RMVar_hsa_circ_92162,RMVar_hsa_circ_103407,RMVar_hsa_circ_180158,RMVar_hsa_circ_180159 22683 RMVar_ID_22683 Human_SNP_ID_610948121 A-to-I Human chr16 + 81029612 81029612 81029612 TGTTTTTTGTTTTTTGAGACAAGTCTCCTTCTATCGCCCAGGCTGGAGTGCAATGGCACAATCTT TGTTTTTTGTTTTTTGAGACAAGTCTCCTTCTTTCGCCCAGGCTGGAGTGCAATGGCACAATCTT A T CENPN Ensembl:ENSG00000166451 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs147211540 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6541123,Human_RBP_ID_17564768,Human_RBP_ID_26445420 RMVar_hsa_circ_91153,RMVar_hsa_circ_180151,RMVar_hsa_circ_92162,RMVar_hsa_circ_103407,RMVar_hsa_circ_180158,RMVar_hsa_circ_180159 22684 RMVar_ID_22684 Human_SNP_ID_610948149 A-to-I Human chr16 + 81029704 81029704 81029704 TTGAAGAGATTCTCCTGCCTCAGCCTCTGAGTAGCTGGGACTACAGGCCTGCACCACCATGCCCA TTGAAGAGATTCTCCTGCCTCAGCCTCTGAGTCGCTGGGACTACAGGCCTGCACCACCATGCCCA A C CENPN Ensembl:ENSG00000166451 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1204433465 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91153,RMVar_hsa_circ_180151,RMVar_hsa_circ_92162,RMVar_hsa_circ_103407,RMVar_hsa_circ_180158,RMVar_hsa_circ_180159 22685 RMVar_ID_22685 Human_SNP_ID_610948193 A-to-I Human chr16 + 81029827 81029827 81029827 AAACTCCTGGGCTCAAGCAATCTGCCCATTTTAGCCTCCTAAAATGCTGGGATTATAGGAGTGTA AAACTCCTGGGCTCAAGCAATCTGCCCATTTTGGCCTCCTAAAATGCTGGGATTATAGGAGTGTA A G CENPN Ensembl:ENSG00000166451 Protein coding intron GSE38233;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29796672,31158229,32596459 RNA-Seq:(High) rs1044131936 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6541126,Human_RBP_ID_23165705,Human_RBP_ID_26446392 RMVar_hsa_circ_91153,RMVar_hsa_circ_180151,RMVar_hsa_circ_92162,RMVar_hsa_circ_103407,RMVar_hsa_circ_180158,RMVar_hsa_circ_180159 22686 RMVar_ID_22686 Human_SNP_ID_610948382 A-to-I Human chr16 + 81030445 81030445 81030445 CCCCCACACATTAAGCAAGTGTGAAACATGATATAGAAAAATGACTTCACTCTGGGCCGGGTGTA CCCCCACACATTAAGCAAGTGTGAAACATGATGTAGAAAAATGACTTCACTCTGGGCCGGGTGTA A G CENPN Ensembl:ENSG00000166451 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs913026467 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18287748 RMVar_hsa_circ_91153,RMVar_hsa_circ_180151,RMVar_hsa_circ_92162,RMVar_hsa_circ_103407,RMVar_hsa_circ_180158,RMVar_hsa_circ_180159 22687 RMVar_ID_22687 Human_SNP_ID_610948429 A-to-I Human chr16 + 81030558 81030558 81030558 ATCACCCGAGGTCAGGAGTTCGAGACCAGCCTAGCCAACATGGCAAAACCTTGTCTCTACTAAAA ATCACCCGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGCAAAACCTTGTCTCTACTAAAA A G CENPN Ensembl:ENSG00000166451 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs1023650404 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91153,RMVar_hsa_circ_180151,RMVar_hsa_circ_92162,RMVar_hsa_circ_103407,RMVar_hsa_circ_180158,RMVar_hsa_circ_180159 22688 RMVar_ID_22688 Human_SNP_ID_610948435 A-to-I Human chr16 + 81030588 81030588 81030588 CTAGCCAACATGGCAAAACCTTGTCTCTACTAAAAATAGAAAAATTAGTTGGGGGTAGTGGCAGC CTAGCCAACATGGCAAAACCTTGTCTCTACTATAAATAGAAAAATTAGTTGGGGGTAGTGGCAGC A T CENPN Ensembl:ENSG00000166451 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs915089247 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91153,RMVar_hsa_circ_180151,RMVar_hsa_circ_92162,RMVar_hsa_circ_103407,RMVar_hsa_circ_180158,RMVar_hsa_circ_180159 22689 RMVar_ID_22689 Human_SNP_ID_610948470 A-to-I Human chr16 + 81030681 81030681 81030681 TGAGGCAGGAGAACTGGTTGAACCGGGGAGGCAGAGGTTGCAGTGAGCCAAGATCATGCCACTGC TGAGGCAGGAGAACTGGTTGAACCGGGGAGGCCGAGGTTGCAGTGAGCCAAGATCATGCCACTGC A C CENPN Ensembl:ENSG00000166451 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1259187806 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91153,RMVar_hsa_circ_180151,RMVar_hsa_circ_92162,RMVar_hsa_circ_103407,RMVar_hsa_circ_180158,RMVar_hsa_circ_180159 22690 RMVar_ID_22690 Human_SNP_ID_610948479 A-to-I Human chr16 + 81030704 81030704 81030704 CGGGGAGGCAGAGGTTGCAGTGAGCCAAGATCATGCCACTGCACTCTAGCCTGGGTGACAGAGTG CGGGGAGGCAGAGGTTGCAGTGAGCCAAGATCGTGCCACTGCACTCTAGCCTGGGTGACAGAGTG A G CENPN Ensembl:ENSG00000166451 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1003256598 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91153,RMVar_hsa_circ_180151,RMVar_hsa_circ_92162,RMVar_hsa_circ_103407,RMVar_hsa_circ_180158,RMVar_hsa_circ_180159 22691 RMVar_ID_22691 Human_SNP_ID_610948502 A-to-I Human chr16 + 81030768 81030768 81030768 GAAACTCTGCCTCAAAAAATAAAATAAAGGCCAGGCATGGTGGCTCACGCCTATAATCCCAGCAC GAAACTCTGCCTCAAAAAATAAAATAAAGGCCGGGCATGGTGGCTCACGCCTATAATCCCAGCAC A G CENPN Ensembl:ENSG00000166451 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs960013495 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91153,RMVar_hsa_circ_180151,RMVar_hsa_circ_92162,RMVar_hsa_circ_103407,RMVar_hsa_circ_180158,RMVar_hsa_circ_180159 22692 RMVar_ID_22692 Human_SNP_ID_610948540 A-to-I Human chr16 + 81030884 81030884 81030884 TTAGCAACATGGTGAAGGTGAACCCCGACTCTACTAAAAATACAAAAATTAGCTGGGCCTGGTGG TTAGCAACATGGTGAAGGTGAACCCCGACTCTCCTAAAAATACAAAAATTAGCTGGGCCTGGTGG A C CENPN,AC092718.4 Ensembl:ENSG00000166451,Ensembl:ENSG00000261061 Protein coding,lincRNA intron,exon GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,29796672,31158229,31158229 RNA-Seq:(High) rs982996019 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91153,RMVar_hsa_circ_180151,RMVar_hsa_circ_92162,RMVar_hsa_circ_103407,RMVar_hsa_circ_180158,RMVar_hsa_circ_180159 22693 RMVar_ID_22693 Human_SNP_ID_610948542 A-to-I Human chr16 + 81030890 81030890 81030890 ACATGGTGAAGGTGAACCCCGACTCTACTAAAAATACAAAAATTAGCTGGGCCTGGTGGTGTGCA ACATGGTGAAGGTGAACCCCGACTCTACTAAACATACAAAAATTAGCTGGGCCTGGTGGTGTGCA A C CENPN,AC092718.4 Ensembl:ENSG00000166451,Ensembl:ENSG00000261061 Protein coding,lincRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1416859451 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91153,RMVar_hsa_circ_180151,RMVar_hsa_circ_92162,RMVar_hsa_circ_103407,RMVar_hsa_circ_180158,RMVar_hsa_circ_180159 22694 RMVar_ID_22694 Human_SNP_ID_610948569 A-to-I Human chr16 + 81030990 81030990 81030990 AGAATCGCTTGAACCCGGGAGACATAGGTTGCAGTGAGCCGAGACTGCACCACTGCACTCCAGCC AGAATCGCTTGAACCCGGGAGACATAGGTTGCGGTGAGCCGAGACTGCACCACTGCACTCCAGCC A G CENPN,AC092718.4 Ensembl:ENSG00000166451,Ensembl:ENSG00000261061 Protein coding,lincRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs370350666 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6541135 RMVar_hsa_circ_91153,RMVar_hsa_circ_180151,RMVar_hsa_circ_92162,RMVar_hsa_circ_103407,RMVar_hsa_circ_180158,RMVar_hsa_circ_180159 22695 RMVar_ID_22695 Human_SNP_ID_610948570 A-to-I Human chr16 + 81030990 81030990 81030990 AGAATCGCTTGAACCCGGGAGACATAGGTTGCAGTGAGCCGAGACTGCACCACTGCACTCCAGCC AGAATCGCTTGAACCCGGGAGACATAGGTTGCTGTGAGCCGAGACTGCACCACTGCACTCCAGCC A T CENPN,AC092718.4 Ensembl:ENSG00000166451,Ensembl:ENSG00000261061 Protein coding,lincRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs370350666 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6541135 RMVar_hsa_circ_91153,RMVar_hsa_circ_180151,RMVar_hsa_circ_92162,RMVar_hsa_circ_103407,RMVar_hsa_circ_180158,RMVar_hsa_circ_180159 22696 RMVar_ID_22696 Human_SNP_ID_610948585 A-to-I Human chr16 + 81031031 81031031 81031031 AGACTGCACCACTGCACTCCAGCCTAGGTGACAGAGTGAGACTCCATCTTAAAAAATAAATAAAT AGACTGCACCACTGCACTCCAGCCTAGGTGACGGAGTGAGACTCCATCTTAAAAAATAAATAAAT A G CENPN,AC092718.4 Ensembl:ENSG00000166451,Ensembl:ENSG00000261061 Protein coding,lincRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs554636447 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91153,RMVar_hsa_circ_180151,RMVar_hsa_circ_92162,RMVar_hsa_circ_103407,RMVar_hsa_circ_180158,RMVar_hsa_circ_180159 22697 RMVar_ID_22697 Human_SNP_ID_610952622 A-to-I Human chr16 - 81043752 81043752 81043752 TGTGCAGAAGGTATAAAGTTTTGTGAGGCATAAGACAGATCTGTCTGCACGTTGATTGAAGAAAT TGTGCAGAAGGTATAAAGTTTTGTGAGGCATACGACAGATCTGTCTGCACGTTGATTGAAGAAAT T G AC092718.8 Ensembl:ENSG00000284512 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1462444963 Functional Loss SNV dbSNP153 33..33 33 - - - 22698 RMVar_ID_22698 Human_SNP_ID_610956158 A-to-I Human chr16 - 81054817 81054817 81054817 ATGGCAAAACCCTGCCTCTACTAAAAATAGAAAAATTAGGGGGCGTGGTGGTGCGTGCCTGTAAT ATGGCAAAACCCTGCCTCTACTAAAAATAGAACAATTAGGGGGCGTGGTGGTGCGTGCCTGTAAT T G C16orf46,AC092718.3,AC092718.8 Ensembl:ENSG00000166455,Ensembl:ENSG00000260643,Ensembl:ENSG00000284512 Protein coding,Protein coding,Protein coding intron,intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs979516960 Functional Loss SNV dbSNP153 33..33 33 - - - 22699 RMVar_ID_22699 Human_SNP_ID_610956160 A-to-I Human chr16 - 81054826 81054820 81054826 CTGGCCAACATGGCAAAACCCTGCCTCTACTAAAAATAGAAAAATTAGGGGGCGTGGTGGTGCGT CTGGCCAACATGGCAAAACCCTGCCTCTACTA______GAAAAATTAGGGGGCGTGGTGGTGCGT CTATTTT C C16orf46,AC092718.3,AC092718.8 Ensembl:ENSG00000166455,Ensembl:ENSG00000260643,Ensembl:ENSG00000284512 Protein coding,Protein coding,Protein coding intron,intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs935392422 Functional Loss DEL dbSNP153 33..38 33 - - - 22700 RMVar_ID_22700 Human_SNP_ID_610956494 A-to-I Human chr16 - 81055991 81055991 81055991 ACAGTTGGCTGGGCATTGTGGCTCGTGCCTGTAATCCCAGGACTTTGGGAGGCTGAGGTGGGTGG ACAGTTGGCTGGGCATTGTGGCTCGTGCCTGTCATCCCAGGACTTTGGGAGGCTGAGGTGGGTGG T G C16orf46,AC092718.3,AC092718.8 Ensembl:ENSG00000166455,Ensembl:ENSG00000260643,Ensembl:ENSG00000284512 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1390304953 Functional Loss SNV dbSNP153 33..33 33 - - - 22701 RMVar_ID_22701 Human_SNP_ID_610960799 A-to-I Human chr16 - 81068883 81068883 81068883 TTGGCCAACATGGTGAAACCCTGTCTCTACTAAAAATACAAAAAAAATTAGCCGGGCGTGGTGGC TTGGCCAACATGGTGAAACCCTGTCTCTACTACAAATACAAAAAAAATTAGCCGGGCGTGGTGGC T G C16orf46,AC092718.3,AC092718.8 Ensembl:ENSG00000166455,Ensembl:ENSG00000260643,Ensembl:ENSG00000284512 Protein coding,Protein coding,Protein coding intron,intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1280564010 Functional Loss SNV dbSNP153 33..33 33 - - - 22702 RMVar_ID_22702 Human_SNP_ID_610965437 A-to-I Human chr16 - 81083352 81083352 81083352 CACCACGCCCAGCTAATTTTTGTGGTTTTGGTAGAGATGGGGTTCCACTATGTTGGCCAGGCTGG CACCACGCCCAGCTAATTTTTGTGGTTTTGGTGGAGATGGGGTTCCACTATGTTGGCCAGGCTGG T C GCSH,AC092718.3,AC092718.8 Ensembl:ENSG00000140905,Ensembl:ENSG00000260643,Ensembl:ENSG00000284512 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232375526 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_762609 22703 RMVar_ID_22703 Human_SNP_ID_610965468 A-to-I Human chr16 - 81083434 81083434 81083434 CGGTGCACTGCAACCTCCCCTTCTCGGGTTCAAGCACTTCTTCTGCCTCAGCTTCCCAGTAGCTG CGGTGCACTGCAACCTCCCCTTCTCGGGTTCACGCACTTCTTCTGCCTCAGCTTCCCAGTAGCTG T G GCSH,AC092718.3,AC092718.8 Ensembl:ENSG00000140905,Ensembl:ENSG00000260643,Ensembl:ENSG00000284512 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs908803381 Functional Loss SNV dbSNP153 33..33 33 - - - 22704 RMVar_ID_22704 Human_SNP_ID_610976209 A-to-I Human chr16 - 81114629 81114627 81114630 AGCTGGGCATGGTGAAGCACGCCTACAGTCCCAGTTACTCAGGAGTCTGAGGCAGGAGAATCGCT AGCTGGGCATGGTGAAGCACGCCTACAGTCC___TTACTCAGGAGTCTGAGGCAGGAGAATCGCT ACTG A PKD1L2 Ensembl:ENSG00000166473 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1389298293 Functional Loss DEL dbSNP153 32..34 33 - - - 22705 RMVar_ID_22705 Human_SNP_ID_610976769 A-to-I Human chr16 - 81116170 81116170 81116170 TTGTTTTTTGAGACGGACTCTTGCATGATCTCAGCTCACTGCAACCTCTCCCTCCTGGGTTCAAG TTGTTTTTTGAGACGGACTCTTGCATGATCTCGGCTCACTGCAACCTCTCCCTCCTGGGTTCAAG T C PKD1L2 Ensembl:ENSG00000166473 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1325547291 Functional Loss SNV dbSNP153 33..33 33 - - - 22706 RMVar_ID_22706 Human_SNP_ID_610992555 A-to-I Human chr16 - 81154611 81154611 81154611 GGCAGTGAGCTAAGATCACGGCACTGTACTCGAGCCTAGGCAGCAGAGCGAGACCCTGTCTGAAA GGCAGTGAGCTAAGATCACGGCACTGTACTCGGGCCTAGGCAGCAGAGCGAGACCCTGTCTGAAA T C PKD1L2 Ensembl:ENSG00000166473 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1457041947 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80943,RMVar_hsa_circ_180162 22707 RMVar_ID_22707 Human_SNP_ID_611029932 A-to-I Human chr16 + 81246669 81246669 81246669 GGTCGGGAGTTTGAGACCAACCTGGCCAACATAGCGAAACCCCATCTCCACCAAAAATACAAAAA GGTCGGGAGTTTGAGACCAACCTGGCCAACATGGCGAAACCCCATCTCCACCAAAAATACAAAAA A G BCO1 Ensembl:ENSG00000135697 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1286553952 Functional Loss SNV dbSNP153 33..33 33 - - - 22708 RMVar_ID_22708 Human_SNP_ID_611073506 A-to-I Human chr16 + 81375888 81375888 81375888 ACTATTTGGGAGGGTGGGGTGAGAGGATCACTAGAGTCCAAGAGGTTGAGACTGCAGTGAGCTGT ACTATTTGGGAGGGTGGGGTGAGAGGATCACTGGAGTCCAAGAGGTTGAGACTGCAGTGAGCTGT A G GAN Ensembl:ENSG00000261609 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs987147542 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_376782,RMVar_hsa_circ_378046,RMVar_hsa_circ_180173,RMVar_hsa_circ_31398,RMVar_hsa_circ_180172,RMVar_hsa_circ_265849,RMVar_hsa_circ_115067,RMVar_hsa_circ_84110,RMVar_hsa_circ_180174,RMVar_hsa_circ_180175,RMVar_hsa_circ_180180,RMVar_hsa_circ_268392 22709 RMVar_ID_22709 Human_SNP_ID_611077438 A-to-I Human chr16 + 81386722 81386722 81386722 TAATCCCAGGACTTTGGGAGGCCAAGGCGGGCAGATCACCTGAGGTCGGCAGTTTGAGACCAGCC TAATCCCAGGACTTTGGGAGGCCAAGGCGGGCGGATCACCTGAGGTCGGCAGTTTGAGACCAGCC A G AC092139.1 Ensembl:ENSG00000272923 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs546196821 Functional Loss SNV dbSNP153 33..33 33 - - - 22710 RMVar_ID_22710 Human_SNP_ID_611077512 A-to-I Human chr16 + 81386924 81386924 81386924 GCCGAGATGGTGCCGTTGCACTCCAGCCGGGCAACAAGGGCTAAACTCCATCTCAAAAGAAAAGA GCCGAGATGGTGCCGTTGCACTCCAGCCGGGCGACAAGGGCTAAACTCCATCTCAAAAGAAAAGA A G AC092139.1 Ensembl:ENSG00000272923 lincRNA exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs35385837 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5097280,Human_RBP_ID_18287842 22711 RMVar_ID_22711 Human_SNP_ID_611117038 A-to-I Human chr16 + 81501705 81501705 81501705 GTGATCTCAGCTCACTGCAACTTCTGCTTCCCAGGTTCTCGCAATTCTCCTGCCTCAGCCTCCCG GTGATCTCAGCTCACTGCAACTTCTGCTTCCCGGGTTCTCGCAATTCTCCTGCCTCAGCCTCCCG A G CMIP Ensembl:ENSG00000153815 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1430633113 Functional Loss SNV dbSNP153 33..33 33 - - - 22712 RMVar_ID_22712 Human_SNP_ID_611215133 A-to-I Human chr16 + 81780448 81780448 81780448 GGCATTCTCTGGGGCATGGGCCCTCGTCCTTGACTACAGTTCTGCGGGGAAGTTTTACAGAATTT GGCATTCTCTGGGGCATGGGCCCTCGTCCTTGGCTACAGTTCTGCGGGGAAGTTTTACAGAATTT A G PLCG2 Ensembl:ENSG00000197943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4410068 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2104,GWAS_ID_2105,GWAS_ID_2106,GWAS_ID_2107 RMVar_hsa_circ_88525,RMVar_hsa_circ_180197 22713 RMVar_ID_22713 Human_SNP_ID_611216101 A-to-I Human chr16 + 81782661 81782661 81782661 ACAAGCTTATTTAGAAGGGCATTTCGTGAGATACAAGAACCCCAAACCAGAAATCAAGGAAGTTT ACAAGCTTATTTAGAAGGGCATTTCGTGAGATCCAAGAACCCCAAACCAGAAATCAAGGAAGTTT A C PLCG2 Ensembl:ENSG00000197943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1284973448 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88525,RMVar_hsa_circ_180197 22714 RMVar_ID_22714 Human_SNP_ID_611216102 A-to-I Human chr16 + 81782661 81782661 81782661 ACAAGCTTATTTAGAAGGGCATTTCGTGAGATACAAGAACCCCAAACCAGAAATCAAGGAAGTTT ACAAGCTTATTTAGAAGGGCATTTCGTGAGATGCAAGAACCCCAAACCAGAAATCAAGGAAGTTT A G PLCG2 Ensembl:ENSG00000197943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1284973448 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88525,RMVar_hsa_circ_180197 22715 RMVar_ID_22715 Human_SNP_ID_611216560 A-to-I Human chr16 + 81783731 81783731 81783731 CAATAAATGGCTGCTTAACAAGGATGAAATGGACCATGGGGGCACCTTGTTCATCCCTTTGTCCT CAATAAATGGCTGCTTAACAAGGATGAAATGGGCCATGGGGGCACCTTGTTCATCCCTTTGTCCT A G PLCG2 Ensembl:ENSG00000197943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4471676 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88525,RMVar_hsa_circ_180197 22716 RMVar_ID_22716 Human_SNP_ID_611219693 A-to-I Human chr16 + 81791845 81791845 81791845 CCCTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAACCACTGCACCCAGCCTTAGCTGGGACTG CCCTGGCCTCCCAAAGTGCTGGGATTACAGGCCTGAACCACTGCACCCAGCCTTAGCTGGGACTG A C PLCG2 Ensembl:ENSG00000197943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1388770708 Functional Loss SNV dbSNP153 33..33 33 - - - 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 22717 RMVar_ID_22717 Human_SNP_ID_611219694 A-to-I Human chr16 + 81791845 81791845 81791845 CCCTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAACCACTGCACCCAGCCTTAGCTGGGACTG CCCTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAACCACTGCACCCAGCCTTAGCTGGGACTG A G PLCG2 Ensembl:ENSG00000197943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1388770708 Functional Loss SNV dbSNP153 33..33 33 - - - 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 22718 RMVar_ID_22718 Human_SNP_ID_611221988 A-to-I Human chr16 + 81797910 81797910 81797910 TGAAGTGCAGCGGCACAATTTCAGTTCACTGCAACCTCTGCCTCCCGGGTTCAAGCAATTATTCT TGAAGTGCAGCGGCACAATTTCAGTTCACTGCCACCTCTGCCTCCCGGGTTCAAGCAATTATTCT A C PLCG2 Ensembl:ENSG00000197943 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1323648182 Functional Loss SNV dbSNP153 33..33 33 - - - 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 22719 RMVar_ID_22719 Human_SNP_ID_611231825 A-to-I Human chr16 + 81822636 81822636 81822636 AAAATTAACTGGGCATGGTGGCGTGTACCTGTAATCCCAGCTACTCAGAAGGCTGAGGCAGGAGA AAAATTAACTGGGCATGGTGGCGTGTACCTGTTATCCCAGCTACTCAGAAGGCTGAGGCAGGAGA A T PLCG2 Ensembl:ENSG00000197943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1337945936 Functional Loss SNV dbSNP153 33..33 33 - - - 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 22720 RMVar_ID_22720 Human_SNP_ID_611232258 A-to-I Human chr16 + 81823655 81823655 81823655 TCAAGCGATCTTCCCGCCTCAGTCTCTCAAGTAGCTGAGACTACAGATGTGCACCACCATGCCCA TCAAGCGATCTTCCCGCCTCAGTCTCTCAAGTTGCTGAGACTACAGATGTGCACCACCATGCCCA A T PLCG2 Ensembl:ENSG00000197943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1010591296 Functional Loss SNV dbSNP153 33..33 33 - - - 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 22721 RMVar_ID_22721 Human_SNP_ID_611232262 A-to-I Human chr16 + 81823665 81823665 81823665 TTCCCGCCTCAGTCTCTCAAGTAGCTGAGACTACAGATGTGCACCACCATGCCCAGCTAATTTTT TTCCCGCCTCAGTCTCTCAAGTAGCTGAGACTGCAGATGTGCACCACCATGCCCAGCTAATTTTT A G PLCG2 Ensembl:ENSG00000197943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1268944095 Functional Loss SNV dbSNP153 33..33 33 - - - 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 22722 RMVar_ID_22722 Human_SNP_ID_611232578 A-to-I Human chr16 + 81824267 81824267 81824267 GCAATTCTCCTCCCTCAGCCTCCCAAGTAACTAGGATTATAGGCATGCGTCACCACACCTGGCTA GCAATTCTCCTCCCTCAGCCTCCCAAGTAACTCGGATTATAGGCATGCGTCACCACACCTGGCTA A C PLCG2 Ensembl:ENSG00000197943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs992757822 Functional Loss SNV dbSNP153 33..33 33 - - - 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 22723 RMVar_ID_22723 Human_SNP_ID_611234622 A-to-I Human chr16 + 81829432 81829432 81829432 TGCCTAGCCAGTTTCACCATGTTGACCAGGCTAGTCTCGAACTCCTAAGCTCAGGTGATCCACCC TGCCTAGCCAGTTTCACCATGTTGACCAGGCTTGTCTCGAACTCCTAAGCTCAGGTGATCCACCC A T PLCG2 Ensembl:ENSG00000197943 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1430370041 Functional Loss SNV dbSNP153 33..33 33 - - - 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 22724 RMVar_ID_22724 Human_SNP_ID_611237952 A-to-I Human chr16 + 81838098 81838098 81838098 CTTTGAAAGATACTAATTTTCTTTTTTTTTTGAGGCGGAGTCTGGCTCTGTTGCCCAGGCTAGAG CTTTGAAAGATACTAATTTTCTTTTTTTTTTGGGGCGGAGTCTGGCTCTGTTGCCCAGGCTAGAG A G PLCG2 Ensembl:ENSG00000197943 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1044602819 Functional Loss SNV dbSNP153 33..33 33 - - - 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 22725 RMVar_ID_22725 Human_SNP_ID_611243136 A-to-I Human chr16 + 81851612 81851612 81851612 TCGGCTCCCTGCAACCTCCGCCTCCCGAGTTCAGGCGATTCTTCTGCCTCATCCTCCCAAGTAGC TCGGCTCCCTGCAACCTCCGCCTCCCGAGTTCGGGCGATTCTTCTGCCTCATCCTCCCAAGTAGC A G PLCG2 Ensembl:ENSG00000197943 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1389006758 Functional Loss SNV dbSNP153 33..33 33 - - - 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 22726 RMVar_ID_22726 Human_SNP_ID_611250969 A-to-I Human chr16 + 81871521 81871521 81871521 CCACCACGCCCAGCTAATTTTGTATTTTTAGTAGAGATGGGGTTTTGCCGCATTGGGTGGGCAGG CCACCACGCCCAGCTAATTTTGTATTTTTAGTGGAGATGGGGTTTTGCCGCATTGGGTGGGCAGG A G PLCG2 Ensembl:ENSG00000197943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs571570830 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92373,RMVar_hsa_circ_88525,RMVar_hsa_circ_109246,RMVar_hsa_circ_180197,RMVar_hsa_circ_180199,RMVar_hsa_circ_180198,RMVar_hsa_circ_97108,RMVar_hsa_circ_46125,RMVar_hsa_circ_106874,RMVar_hsa_circ_12730,RMVar_hsa_circ_180202,RMVar_hsa_circ_113603,RMVar_hsa_circ_123514,RMVar_hsa_circ_87552,RMVar_hsa_circ_89974,RMVar_hsa_circ_180204,RMVar_hsa_circ_180205,RMVar_hsa_circ_180206,RMVar_hsa_circ_180203,RMVar_hsa_circ_95751,RMVar_hsa_circ_180207,RMVar_hsa_circ_104764,RMVar_hsa_circ_119840,RMVar_hsa_circ_180209,RMVar_hsa_circ_180210,RMVar_hsa_circ_180211 22727 RMVar_ID_22727 Human_SNP_ID_611252792 A-to-I Human chr16 + 81876089 81876089 81876089 ACTTTGTCACCGAGGCTGGGGTGCAGTGGTACAATCATGGCTCACTGCAGCCTCGAACTCCCTGG ACTTTGTCACCGAGGCTGGGGTGCAGTGGTACTATCATGGCTCACTGCAGCCTCGAACTCCCTGG A T PLCG2 Ensembl:ENSG00000197943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs571740589 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92373,RMVar_hsa_circ_88525,RMVar_hsa_circ_109246,RMVar_hsa_circ_180197,RMVar_hsa_circ_180199,RMVar_hsa_circ_180198,RMVar_hsa_circ_97108,RMVar_hsa_circ_46125,RMVar_hsa_circ_106874,RMVar_hsa_circ_12730,RMVar_hsa_circ_180202,RMVar_hsa_circ_113603,RMVar_hsa_circ_123514,RMVar_hsa_circ_87552,RMVar_hsa_circ_89974,RMVar_hsa_circ_180204,RMVar_hsa_circ_180205,RMVar_hsa_circ_180206,RMVar_hsa_circ_180203,RMVar_hsa_circ_95751,RMVar_hsa_circ_180207,RMVar_hsa_circ_104764,RMVar_hsa_circ_119840,RMVar_hsa_circ_180209,RMVar_hsa_circ_180210,RMVar_hsa_circ_180211 22728 RMVar_ID_22728 Human_SNP_ID_611252837 A-to-I Human chr16 + 81876199 81876199 81876199 AGGCGTGTGCCACCATGCAGGCTAATTTTTGTATTTTTTGTAGAGACAGTTTCACCATGTTACCC AGGCGTGTGCCACCATGCAGGCTAATTTTTGTGTTTTTTGTAGAGACAGTTTCACCATGTTACCC A G PLCG2 Ensembl:ENSG00000197943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs535563729 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92373,RMVar_hsa_circ_88525,RMVar_hsa_circ_109246,RMVar_hsa_circ_180197,RMVar_hsa_circ_180199,RMVar_hsa_circ_180198,RMVar_hsa_circ_97108,RMVar_hsa_circ_46125,RMVar_hsa_circ_106874,RMVar_hsa_circ_12730,RMVar_hsa_circ_180202,RMVar_hsa_circ_113603,RMVar_hsa_circ_123514,RMVar_hsa_circ_87552,RMVar_hsa_circ_89974,RMVar_hsa_circ_180204,RMVar_hsa_circ_180205,RMVar_hsa_circ_180206,RMVar_hsa_circ_180203,RMVar_hsa_circ_95751,RMVar_hsa_circ_180207,RMVar_hsa_circ_104764,RMVar_hsa_circ_119840,RMVar_hsa_circ_180209,RMVar_hsa_circ_180210,RMVar_hsa_circ_180211 22729 RMVar_ID_22729 Human_SNP_ID_611254045 A-to-I Human chr16 + 81878900 81878900 81878900 CATTCTCTGTCCTGCTCTGCGTCCCAGGGGCCAATTCCTGCAAACACGTTCCCAGGTGCCTGTGC CATTCTCTGTCCTGCTCTGCGTCCCAGGGGCCGATTCCTGCAAACACGTTCCCAGGTGCCTGTGC A G PLCG2 Ensembl:ENSG00000197943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs8062348 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92373,RMVar_hsa_circ_88525,RMVar_hsa_circ_109246,RMVar_hsa_circ_180197,RMVar_hsa_circ_180199,RMVar_hsa_circ_180198,RMVar_hsa_circ_97108,RMVar_hsa_circ_46125,RMVar_hsa_circ_106874,RMVar_hsa_circ_12730,RMVar_hsa_circ_180202,RMVar_hsa_circ_113603,RMVar_hsa_circ_123514,RMVar_hsa_circ_87552,RMVar_hsa_circ_89974,RMVar_hsa_circ_180204,RMVar_hsa_circ_180205,RMVar_hsa_circ_180206,RMVar_hsa_circ_180203,RMVar_hsa_circ_95751,RMVar_hsa_circ_180207,RMVar_hsa_circ_104764,RMVar_hsa_circ_119840,RMVar_hsa_circ_180209,RMVar_hsa_circ_180210,RMVar_hsa_circ_180211 22730 RMVar_ID_22730 Human_SNP_ID_611254046 A-to-I Human chr16 + 81878900 81878900 81878900 CATTCTCTGTCCTGCTCTGCGTCCCAGGGGCCAATTCCTGCAAACACGTTCCCAGGTGCCTGTGC CATTCTCTGTCCTGCTCTGCGTCCCAGGGGCCTATTCCTGCAAACACGTTCCCAGGTGCCTGTGC A T PLCG2 Ensembl:ENSG00000197943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs8062348 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92373,RMVar_hsa_circ_88525,RMVar_hsa_circ_109246,RMVar_hsa_circ_180197,RMVar_hsa_circ_180199,RMVar_hsa_circ_180198,RMVar_hsa_circ_97108,RMVar_hsa_circ_46125,RMVar_hsa_circ_106874,RMVar_hsa_circ_12730,RMVar_hsa_circ_180202,RMVar_hsa_circ_113603,RMVar_hsa_circ_123514,RMVar_hsa_circ_87552,RMVar_hsa_circ_89974,RMVar_hsa_circ_180204,RMVar_hsa_circ_180205,RMVar_hsa_circ_180206,RMVar_hsa_circ_180203,RMVar_hsa_circ_95751,RMVar_hsa_circ_180207,RMVar_hsa_circ_104764,RMVar_hsa_circ_119840,RMVar_hsa_circ_180209,RMVar_hsa_circ_180210,RMVar_hsa_circ_180211 22731 RMVar_ID_22731 Human_SNP_ID_611257464 A-to-I Human chr16 + 81887387 81887387 81887387 ATGATCCGCCCACCTCGGCCTCCCAAAGTGCTAGGATTACAGGCATGAGCCACCACGCCCGGCCT ATGATCCGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCACGCCCGGCCT A G PLCG2 Ensembl:ENSG00000197943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs995738393 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92373,RMVar_hsa_circ_88525,RMVar_hsa_circ_109246,RMVar_hsa_circ_180197,RMVar_hsa_circ_180199,RMVar_hsa_circ_180198,RMVar_hsa_circ_97108,RMVar_hsa_circ_46125,RMVar_hsa_circ_106874,RMVar_hsa_circ_12730,RMVar_hsa_circ_180202,RMVar_hsa_circ_113603,RMVar_hsa_circ_123514,RMVar_hsa_circ_87552,RMVar_hsa_circ_180204,RMVar_hsa_circ_180205,RMVar_hsa_circ_180206,RMVar_hsa_circ_95751,RMVar_hsa_circ_180207,RMVar_hsa_circ_104764,RMVar_hsa_circ_119840,RMVar_hsa_circ_180209,RMVar_hsa_circ_180210,RMVar_hsa_circ_82259,RMVar_hsa_circ_180211,RMVar_hsa_circ_180213,RMVar_hsa_circ_180212,RMVar_hsa_circ_379091 22732 RMVar_ID_22732 Human_SNP_ID_611257727 A-to-I Human chr16 + 81888234 81888233 81888235 CACGGTCAGAGTACTTTCTTTTTTTTTGAGACAGAGTTTCACTCTGTTGTCCAGGCTGGAGTGCA CACGGTCAGAGTACTTTCTTTTTTTTTGAGAC__AGTTTCACTCTGTTGTCCAGGCTGGAGTGCA CAG C PLCG2 Ensembl:ENSG00000197943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1249697787 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_92373,RMVar_hsa_circ_88525,RMVar_hsa_circ_109246,RMVar_hsa_circ_180197,RMVar_hsa_circ_180199,RMVar_hsa_circ_180198,RMVar_hsa_circ_97108,RMVar_hsa_circ_46125,RMVar_hsa_circ_106874,RMVar_hsa_circ_12730,RMVar_hsa_circ_180202,RMVar_hsa_circ_113603,RMVar_hsa_circ_123514,RMVar_hsa_circ_87552,RMVar_hsa_circ_180204,RMVar_hsa_circ_180205,RMVar_hsa_circ_180206,RMVar_hsa_circ_95751,RMVar_hsa_circ_180207,RMVar_hsa_circ_104764,RMVar_hsa_circ_119840,RMVar_hsa_circ_180209,RMVar_hsa_circ_180210,RMVar_hsa_circ_82259,RMVar_hsa_circ_180211,RMVar_hsa_circ_180213,RMVar_hsa_circ_180212,RMVar_hsa_circ_379091 22733 RMVar_ID_22733 Human_SNP_ID_611258766 A-to-I Human chr16 + 81891083 81891083 81891083 TGCTTGGGAGGTTGAGGCAGGAGAATCGCTTCAACCCAGGAGGTGGAGGTTGCAGTGAGCTGAAA TGCTTGGGAGGTTGAGGCAGGAGAATCGCTTCCACCCAGGAGGTGGAGGTTGCAGTGAGCTGAAA A C PLCG2 Ensembl:ENSG00000197943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1490338895 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92373,RMVar_hsa_circ_88525,RMVar_hsa_circ_109246,RMVar_hsa_circ_180197,RMVar_hsa_circ_180199,RMVar_hsa_circ_180198,RMVar_hsa_circ_97108,RMVar_hsa_circ_46125,RMVar_hsa_circ_106874,RMVar_hsa_circ_180202,RMVar_hsa_circ_113603,RMVar_hsa_circ_123514,RMVar_hsa_circ_87552,RMVar_hsa_circ_180204,RMVar_hsa_circ_180205,RMVar_hsa_circ_180206,RMVar_hsa_circ_95751,RMVar_hsa_circ_180207,RMVar_hsa_circ_104764,RMVar_hsa_circ_119840,RMVar_hsa_circ_180209,RMVar_hsa_circ_180210,RMVar_hsa_circ_82259,RMVar_hsa_circ_180211,RMVar_hsa_circ_64533,RMVar_hsa_circ_123831,RMVar_hsa_circ_180213,RMVar_hsa_circ_180212,RMVar_hsa_circ_379091,RMVar_hsa_circ_330299,RMVar_hsa_circ_339689,RMVar_hsa_circ_81483,RMVar_hsa_circ_180215,RMVar_hsa_circ_180216,RMVar_hsa_circ_180217,RMVar_hsa_circ_180214 22734 RMVar_ID_22734 Human_SNP_ID_611258767 A-to-I Human chr16 + 81891083 81891083 81891083 TGCTTGGGAGGTTGAGGCAGGAGAATCGCTTCAACCCAGGAGGTGGAGGTTGCAGTGAGCTGAAA TGCTTGGGAGGTTGAGGCAGGAGAATCGCTTCTACCCAGGAGGTGGAGGTTGCAGTGAGCTGAAA A T PLCG2 Ensembl:ENSG00000197943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1490338895 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92373,RMVar_hsa_circ_88525,RMVar_hsa_circ_109246,RMVar_hsa_circ_180197,RMVar_hsa_circ_180199,RMVar_hsa_circ_180198,RMVar_hsa_circ_97108,RMVar_hsa_circ_46125,RMVar_hsa_circ_106874,RMVar_hsa_circ_180202,RMVar_hsa_circ_113603,RMVar_hsa_circ_123514,RMVar_hsa_circ_87552,RMVar_hsa_circ_180204,RMVar_hsa_circ_180205,RMVar_hsa_circ_180206,RMVar_hsa_circ_95751,RMVar_hsa_circ_180207,RMVar_hsa_circ_104764,RMVar_hsa_circ_119840,RMVar_hsa_circ_180209,RMVar_hsa_circ_180210,RMVar_hsa_circ_82259,RMVar_hsa_circ_180211,RMVar_hsa_circ_64533,RMVar_hsa_circ_123831,RMVar_hsa_circ_180213,RMVar_hsa_circ_180212,RMVar_hsa_circ_379091,RMVar_hsa_circ_330299,RMVar_hsa_circ_339689,RMVar_hsa_circ_81483,RMVar_hsa_circ_180215,RMVar_hsa_circ_180216,RMVar_hsa_circ_180217,RMVar_hsa_circ_180214 22735 RMVar_ID_22735 Human_SNP_ID_611260879 A-to-I Human chr16 + 81896326 81896326 81896326 TGAGGTGTGATCACTGAGGTCAGGAGTTCGAGAAGAGCCTGGGCAACATGGTGAAACCCCTTCTC TGAGGTGTGATCACTGAGGTCAGGAGTTCGAGGAGAGCCTGGGCAACATGGTGAAACCCCTTCTC A G PLCG2 Ensembl:ENSG00000197943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs926719405 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92373,RMVar_hsa_circ_88525,RMVar_hsa_circ_109246,RMVar_hsa_circ_180197,RMVar_hsa_circ_180199,RMVar_hsa_circ_180198,RMVar_hsa_circ_97108,RMVar_hsa_circ_113603,RMVar_hsa_circ_123514,RMVar_hsa_circ_180205,RMVar_hsa_circ_180206,RMVar_hsa_circ_95751,RMVar_hsa_circ_180207,RMVar_hsa_circ_180210,RMVar_hsa_circ_82259,RMVar_hsa_circ_89702,RMVar_hsa_circ_64533,RMVar_hsa_circ_123831,RMVar_hsa_circ_180212,RMVar_hsa_circ_81483,RMVar_hsa_circ_180216,RMVar_hsa_circ_180217,RMVar_hsa_circ_356037,RMVar_hsa_circ_118936,RMVar_hsa_circ_268522,RMVar_hsa_circ_337333,RMVar_hsa_circ_366200,RMVar_hsa_circ_269002,RMVar_hsa_circ_112255,RMVar_hsa_circ_115097,RMVar_hsa_circ_96321,RMVar_hsa_circ_180221,RMVar_hsa_circ_180223,RMVar_hsa_circ_180225,RMVar_hsa_circ_180226,RMVar_hsa_circ_180224,RMVar_hsa_circ_180222,RMVar_hsa_circ_180220 22736 RMVar_ID_22736 Human_SNP_ID_611261454 A-to-I Human chr16 + 81897691 81897691 81897691 TCTCAGCCTCCCGAGTAGCTGGGATTATAGGCATCCACCATCATGCCCGGCTAATTTGTGTATTT TCTCAGCCTCCCGAGTAGCTGGGATTATAGGCGTCCACCATCATGCCCGGCTAATTTGTGTATTT A G PLCG2 Ensembl:ENSG00000197943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1370298472 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92373,RMVar_hsa_circ_88525,RMVar_hsa_circ_109246,RMVar_hsa_circ_180197,RMVar_hsa_circ_180199,RMVar_hsa_circ_180198,RMVar_hsa_circ_97108,RMVar_hsa_circ_113603,RMVar_hsa_circ_123514,RMVar_hsa_circ_180205,RMVar_hsa_circ_180206,RMVar_hsa_circ_95751,RMVar_hsa_circ_180207,RMVar_hsa_circ_180210,RMVar_hsa_circ_82259,RMVar_hsa_circ_89702,RMVar_hsa_circ_64533,RMVar_hsa_circ_123831,RMVar_hsa_circ_180212,RMVar_hsa_circ_81483,RMVar_hsa_circ_180216,RMVar_hsa_circ_180217,RMVar_hsa_circ_356037,RMVar_hsa_circ_118936,RMVar_hsa_circ_268522,RMVar_hsa_circ_337333,RMVar_hsa_circ_366200,RMVar_hsa_circ_269002,RMVar_hsa_circ_112255,RMVar_hsa_circ_115097,RMVar_hsa_circ_96321,RMVar_hsa_circ_180221,RMVar_hsa_circ_180223,RMVar_hsa_circ_180225,RMVar_hsa_circ_180226,RMVar_hsa_circ_180224,RMVar_hsa_circ_180222,RMVar_hsa_circ_180220 22737 RMVar_ID_22737 Human_SNP_ID_611261893 A-to-I Human chr16 + 81898929 81898929 81898929 AATATAGGCTGGGCACAGTGGCTCACGCCTGTAATCCCAGCACTTTCGGAGGCTGAGGCGGGTGG AATATAGGCTGGGCACAGTGGCTCACGCCTGTGATCCCAGCACTTTCGGAGGCTGAGGCGGGTGG A G PLCG2 Ensembl:ENSG00000197943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs971506923 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92373,RMVar_hsa_circ_88525,RMVar_hsa_circ_109246,RMVar_hsa_circ_180197,RMVar_hsa_circ_180199,RMVar_hsa_circ_180198,RMVar_hsa_circ_97108,RMVar_hsa_circ_113603,RMVar_hsa_circ_123514,RMVar_hsa_circ_180205,RMVar_hsa_circ_180206,RMVar_hsa_circ_95751,RMVar_hsa_circ_180207,RMVar_hsa_circ_180210,RMVar_hsa_circ_82259,RMVar_hsa_circ_89702,RMVar_hsa_circ_64533,RMVar_hsa_circ_123831,RMVar_hsa_circ_180212,RMVar_hsa_circ_81483,RMVar_hsa_circ_180216,RMVar_hsa_circ_180217,RMVar_hsa_circ_356037,RMVar_hsa_circ_118936,RMVar_hsa_circ_268522,RMVar_hsa_circ_337333,RMVar_hsa_circ_366200,RMVar_hsa_circ_269002,RMVar_hsa_circ_112255,RMVar_hsa_circ_115097,RMVar_hsa_circ_96321,RMVar_hsa_circ_180221,RMVar_hsa_circ_180223,RMVar_hsa_circ_180225,RMVar_hsa_circ_180226,RMVar_hsa_circ_180224,RMVar_hsa_circ_180222,RMVar_hsa_circ_180220 22738 RMVar_ID_22738 Human_SNP_ID_611264423 A-to-I Human chr16 + 81905799 81905799 81905799 TCCCACCTCAACCTCCCTGAGTCTCTGGGACCACACGTGCGCACCACCATGCCTGGCTAATTTTT TCCCACCTCAACCTCCCTGAGTCTCTGGGACCGCACGTGCGCACCACCATGCCTGGCTAATTTTT A G PLCG2 Ensembl:ENSG00000197943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4552019 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92373,RMVar_hsa_circ_88525,RMVar_hsa_circ_109246,RMVar_hsa_circ_180197,RMVar_hsa_circ_180199,RMVar_hsa_circ_180198,RMVar_hsa_circ_97108,RMVar_hsa_circ_113603,RMVar_hsa_circ_123514,RMVar_hsa_circ_180205,RMVar_hsa_circ_180206,RMVar_hsa_circ_180207,RMVar_hsa_circ_82259,RMVar_hsa_circ_89702,RMVar_hsa_circ_64533,RMVar_hsa_circ_123831,RMVar_hsa_circ_180212,RMVar_hsa_circ_81483,RMVar_hsa_circ_180216,RMVar_hsa_circ_180217,RMVar_hsa_circ_356037,RMVar_hsa_circ_118936,RMVar_hsa_circ_337333,RMVar_hsa_circ_269002,RMVar_hsa_circ_115097,RMVar_hsa_circ_96321,RMVar_hsa_circ_180221,RMVar_hsa_circ_180223,RMVar_hsa_circ_180224,RMVar_hsa_circ_180222,RMVar_hsa_circ_354606,RMVar_hsa_circ_180220,RMVar_hsa_circ_267322 22739 RMVar_ID_22739 Human_SNP_ID_611264424 A-to-I Human chr16 + 81905799 81905799 81905799 TCCCACCTCAACCTCCCTGAGTCTCTGGGACCACACGTGCGCACCACCATGCCTGGCTAATTTTT TCCCACCTCAACCTCCCTGAGTCTCTGGGACCTCACGTGCGCACCACCATGCCTGGCTAATTTTT A T PLCG2 Ensembl:ENSG00000197943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4552019 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92373,RMVar_hsa_circ_88525,RMVar_hsa_circ_109246,RMVar_hsa_circ_180197,RMVar_hsa_circ_180199,RMVar_hsa_circ_180198,RMVar_hsa_circ_97108,RMVar_hsa_circ_113603,RMVar_hsa_circ_123514,RMVar_hsa_circ_180205,RMVar_hsa_circ_180206,RMVar_hsa_circ_180207,RMVar_hsa_circ_82259,RMVar_hsa_circ_89702,RMVar_hsa_circ_64533,RMVar_hsa_circ_123831,RMVar_hsa_circ_180212,RMVar_hsa_circ_81483,RMVar_hsa_circ_180216,RMVar_hsa_circ_180217,RMVar_hsa_circ_356037,RMVar_hsa_circ_118936,RMVar_hsa_circ_337333,RMVar_hsa_circ_269002,RMVar_hsa_circ_115097,RMVar_hsa_circ_96321,RMVar_hsa_circ_180221,RMVar_hsa_circ_180223,RMVar_hsa_circ_180224,RMVar_hsa_circ_180222,RMVar_hsa_circ_354606,RMVar_hsa_circ_180220,RMVar_hsa_circ_267322 22740 RMVar_ID_22740 Human_SNP_ID_611264691 A-to-I Human chr16 + 81906598 81906598 81906598 GATGTGCACCACCATGCCCTGCTAATTTTTGTAGCCTTAGTAGAGATAGTGTTTCGCCATGTTGG GATGTGCACCACCATGCCCTGCTAATTTTTGTGGCCTTAGTAGAGATAGTGTTTCGCCATGTTGG A G PLCG2 Ensembl:ENSG00000197943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1002559582 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92373,RMVar_hsa_circ_88525,RMVar_hsa_circ_109246,RMVar_hsa_circ_180197,RMVar_hsa_circ_180199,RMVar_hsa_circ_180198,RMVar_hsa_circ_97108,RMVar_hsa_circ_113603,RMVar_hsa_circ_123514,RMVar_hsa_circ_180205,RMVar_hsa_circ_180206,RMVar_hsa_circ_180207,RMVar_hsa_circ_82259,RMVar_hsa_circ_89702,RMVar_hsa_circ_64533,RMVar_hsa_circ_123831,RMVar_hsa_circ_180212,RMVar_hsa_circ_81483,RMVar_hsa_circ_180216,RMVar_hsa_circ_180217,RMVar_hsa_circ_356037,RMVar_hsa_circ_118936,RMVar_hsa_circ_337333,RMVar_hsa_circ_269002,RMVar_hsa_circ_115097,RMVar_hsa_circ_96321,RMVar_hsa_circ_180221,RMVar_hsa_circ_180223,RMVar_hsa_circ_180224,RMVar_hsa_circ_180222,RMVar_hsa_circ_354606,RMVar_hsa_circ_180220,RMVar_hsa_circ_267322 22741 RMVar_ID_22741 Human_SNP_ID_611264692 A-to-I Human chr16 + 81906598 81906598 81906598 GATGTGCACCACCATGCCCTGCTAATTTTTGTAGCCTTAGTAGAGATAGTGTTTCGCCATGTTGG GATGTGCACCACCATGCCCTGCTAATTTTTGTTGCCTTAGTAGAGATAGTGTTTCGCCATGTTGG A T PLCG2 Ensembl:ENSG00000197943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1002559582 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92373,RMVar_hsa_circ_88525,RMVar_hsa_circ_109246,RMVar_hsa_circ_180197,RMVar_hsa_circ_180199,RMVar_hsa_circ_180198,RMVar_hsa_circ_97108,RMVar_hsa_circ_113603,RMVar_hsa_circ_123514,RMVar_hsa_circ_180205,RMVar_hsa_circ_180206,RMVar_hsa_circ_180207,RMVar_hsa_circ_82259,RMVar_hsa_circ_89702,RMVar_hsa_circ_64533,RMVar_hsa_circ_123831,RMVar_hsa_circ_180212,RMVar_hsa_circ_81483,RMVar_hsa_circ_180216,RMVar_hsa_circ_180217,RMVar_hsa_circ_356037,RMVar_hsa_circ_118936,RMVar_hsa_circ_337333,RMVar_hsa_circ_269002,RMVar_hsa_circ_115097,RMVar_hsa_circ_96321,RMVar_hsa_circ_180221,RMVar_hsa_circ_180223,RMVar_hsa_circ_180224,RMVar_hsa_circ_180222,RMVar_hsa_circ_354606,RMVar_hsa_circ_180220,RMVar_hsa_circ_267322 22742 RMVar_ID_22742 Human_SNP_ID_611264696 A-to-I Human chr16 + 81906604 81906604 81906604 CACCACCATGCCCTGCTAATTTTTGTAGCCTTAGTAGAGATAGTGTTTCGCCATGTTGGCCAGGC CACCACCATGCCCTGCTAATTTTTGTAGCCTTGGTAGAGATAGTGTTTCGCCATGTTGGCCAGGC A G PLCG2 Ensembl:ENSG00000197943 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs531411435 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92373,RMVar_hsa_circ_88525,RMVar_hsa_circ_109246,RMVar_hsa_circ_180197,RMVar_hsa_circ_180199,RMVar_hsa_circ_180198,RMVar_hsa_circ_97108,RMVar_hsa_circ_113603,RMVar_hsa_circ_123514,RMVar_hsa_circ_180205,RMVar_hsa_circ_180206,RMVar_hsa_circ_180207,RMVar_hsa_circ_82259,RMVar_hsa_circ_89702,RMVar_hsa_circ_64533,RMVar_hsa_circ_123831,RMVar_hsa_circ_180212,RMVar_hsa_circ_81483,RMVar_hsa_circ_180216,RMVar_hsa_circ_180217,RMVar_hsa_circ_356037,RMVar_hsa_circ_118936,RMVar_hsa_circ_337333,RMVar_hsa_circ_269002,RMVar_hsa_circ_115097,RMVar_hsa_circ_96321,RMVar_hsa_circ_180221,RMVar_hsa_circ_180223,RMVar_hsa_circ_180224,RMVar_hsa_circ_180222,RMVar_hsa_circ_354606,RMVar_hsa_circ_180220,RMVar_hsa_circ_267322 22743 RMVar_ID_22743 Human_SNP_ID_611264766 A-to-I Human chr16 + 81906784 81906784 81906784 AAGTTGGGCCAGGCGCGATGGCTCATGCCTATAATCCTAGCACCTTGGGAGGCCGAGGAAGGCAG AAGTTGGGCCAGGCGCGATGGCTCATGCCTATGATCCTAGCACCTTGGGAGGCCGAGGAAGGCAG A G PLCG2 Ensembl:ENSG00000197943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs772413833 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92373,RMVar_hsa_circ_88525,RMVar_hsa_circ_109246,RMVar_hsa_circ_180197,RMVar_hsa_circ_180199,RMVar_hsa_circ_180198,RMVar_hsa_circ_97108,RMVar_hsa_circ_113603,RMVar_hsa_circ_123514,RMVar_hsa_circ_180205,RMVar_hsa_circ_180206,RMVar_hsa_circ_180207,RMVar_hsa_circ_82259,RMVar_hsa_circ_89702,RMVar_hsa_circ_64533,RMVar_hsa_circ_123831,RMVar_hsa_circ_180212,RMVar_hsa_circ_81483,RMVar_hsa_circ_180216,RMVar_hsa_circ_180217,RMVar_hsa_circ_356037,RMVar_hsa_circ_118936,RMVar_hsa_circ_337333,RMVar_hsa_circ_269002,RMVar_hsa_circ_115097,RMVar_hsa_circ_96321,RMVar_hsa_circ_180221,RMVar_hsa_circ_180223,RMVar_hsa_circ_180224,RMVar_hsa_circ_180222,RMVar_hsa_circ_354606,RMVar_hsa_circ_180220,RMVar_hsa_circ_267322 22744 RMVar_ID_22744 Human_SNP_ID_611273052 A-to-I Human chr16 + 81929495 81929495 81929495 TTGGCTCACTGCAACCTCTGCCTCCTGGATTCAAGTGATTCTCCTGCCTCAGCCTCCTGAGTAGC TTGGCTCACTGCAACCTCTGCCTCCTGGATTCCAGTGATTCTCCTGCCTCAGCCTCCTGAGTAGC A C PLCG2 Ensembl:ENSG00000197943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1009171652 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92373,RMVar_hsa_circ_180199,RMVar_hsa_circ_113603,RMVar_hsa_circ_180206,RMVar_hsa_circ_123831,RMVar_hsa_circ_180217,RMVar_hsa_circ_118936,RMVar_hsa_circ_115097,RMVar_hsa_circ_180221,RMVar_hsa_circ_180220,RMVar_hsa_circ_267322,RMVar_hsa_circ_94489,RMVar_hsa_circ_69055,RMVar_hsa_circ_180231,RMVar_hsa_circ_64703 22745 RMVar_ID_22745 Human_SNP_ID_611273097 A-to-I Human chr16 + 81929616 81929616 81929616 TAGGGTTTCGCCATGTGGGCCAGGCTGGTCTCAAACTGCTGACCTCAAGTGATCTGCCTGCCTTA TAGGGTTTCGCCATGTGGGCCAGGCTGGTCTCTAACTGCTGACCTCAAGTGATCTGCCTGCCTTA A T PLCG2 Ensembl:ENSG00000197943 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs989853870 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92373,RMVar_hsa_circ_180199,RMVar_hsa_circ_113603,RMVar_hsa_circ_180206,RMVar_hsa_circ_123831,RMVar_hsa_circ_180217,RMVar_hsa_circ_118936,RMVar_hsa_circ_115097,RMVar_hsa_circ_180221,RMVar_hsa_circ_180220,RMVar_hsa_circ_267322,RMVar_hsa_circ_94489,RMVar_hsa_circ_69055,RMVar_hsa_circ_180231,RMVar_hsa_circ_64703 22746 RMVar_ID_22746 Human_SNP_ID_611273395 A-to-I Human chr16 + 81930585 81930585 81930585 GCCCTGGGCAACATGGCGAAACCCCTCTCTACAAAAAATACAAAAATTAGCCAGGCTTTGTGGTG GCCCTGGGCAACATGGCGAAACCCCTCTCTACGAAAAATACAAAAATTAGCCAGGCTTTGTGGTG A G PLCG2 Ensembl:ENSG00000197943 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928602517 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92373,RMVar_hsa_circ_180199,RMVar_hsa_circ_113603,RMVar_hsa_circ_180206,RMVar_hsa_circ_123831,RMVar_hsa_circ_180217,RMVar_hsa_circ_118936,RMVar_hsa_circ_115097,RMVar_hsa_circ_180221,RMVar_hsa_circ_180220,RMVar_hsa_circ_267322,RMVar_hsa_circ_94489,RMVar_hsa_circ_69055,RMVar_hsa_circ_180231,RMVar_hsa_circ_64703 22747 RMVar_ID_22747 Human_SNP_ID_611354205 A-to-I Human chr16 - 82159635 82159635 82159635 TTGGGAGGCCGAGGCAGGCGGATCACGACGTCAGGAGATCGAGACCATCATGGTTAACATGGTGA TTGGGAGGCCGAGGCAGGCGGATCACGACGTCGGGAGATCGAGACCATCATGGTTAACATGGTGA T C MPHOSPH6 Ensembl:ENSG00000135698 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs980972004 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126209,RMVar_hsa_circ_21575,RMVar_hsa_circ_180233 22748 RMVar_ID_22748 Human_SNP_ID_612021335 A-to-I Human chr16 + 83964040 83964040 83964040 TTTGACTACATATAGGCTGGGTGCGGTGGCGCAAGCCTGTAATCCCAGCACTTTGGGAGGCCGAG TTTGACTACATATAGGCTGGGTGCGGTGGCGCCAGCCTGTAATCCCAGCACTTTGGGAGGCCGAG A C OSGIN1 Ensembl:ENSG00000140961 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1448250560 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126880,RMVar_hsa_circ_180261,RMVar_hsa_circ_180262,RMVar_hsa_circ_111798,RMVar_hsa_circ_107176,RMVar_hsa_circ_180263 22749 RMVar_ID_22749 Human_SNP_ID_612021373 A-to-I Human chr16 + 83964165 83964165 83964165 ATCTCTAATAAAAATACAAAAATTAGCCAGGTATGGCGCTGCATGCCTGTAGTTCCAGCTGCTCA ATCTCTAATAAAAATACAAAAATTAGCCAGGTGTGGCGCTGCATGCCTGTAGTTCCAGCTGCTCA A G OSGIN1 Ensembl:ENSG00000140961 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1324063852 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126880,RMVar_hsa_circ_180261,RMVar_hsa_circ_180262,RMVar_hsa_circ_111798,RMVar_hsa_circ_107176,RMVar_hsa_circ_180263 22750 RMVar_ID_22750 Human_SNP_ID_612021380 A-to-I Human chr16 + 83964183 83964183 83964183 AAAATTAGCCAGGTATGGCGCTGCATGCCTGTAGTTCCAGCTGCTCAGGAGGCCGAGGTATGAGA AAAATTAGCCAGGTATGGCGCTGCATGCCTGTCGTTCCAGCTGCTCAGGAGGCCGAGGTATGAGA A C OSGIN1 Ensembl:ENSG00000140961 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1288435871 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126880,RMVar_hsa_circ_180261,RMVar_hsa_circ_180262,RMVar_hsa_circ_111798,RMVar_hsa_circ_107176,RMVar_hsa_circ_180263 22751 RMVar_ID_22751 Human_SNP_ID_612021384 A-to-I Human chr16 + 83964197 83964197 83964197 ATGGCGCTGCATGCCTGTAGTTCCAGCTGCTCAGGAGGCCGAGGTATGAGAATCACCTGAGCCCG ATGGCGCTGCATGCCTGTAGTTCCAGCTGCTCGGGAGGCCGAGGTATGAGAATCACCTGAGCCCG A G OSGIN1 Ensembl:ENSG00000140961 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs926624805 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126880,RMVar_hsa_circ_180261,RMVar_hsa_circ_180262,RMVar_hsa_circ_111798,RMVar_hsa_circ_107176,RMVar_hsa_circ_180263 22752 RMVar_ID_22752 Human_SNP_ID_612089344 A-to-I Human chr16 - 84114612 84114612 84114612 TTGGTCAGGCTGGTTTCAGACTCCTTGACCTCATGATCCGCCCGCGTCGGCCTCCCAAAGTGCTG TTGGTCAGGCTGGTTTCAGACTCCTTGACCTCGTGATCCGCCCGCGTCGGCCTCCCAAAGTGCTG T C MBTPS1 Ensembl:ENSG00000140943 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs914929846 Functional Loss SNV dbSNP153 33..33 33 - - - 22753 RMVar_ID_22753 Human_SNP_ID_612095439 A-to-I Human chr16 - 84131131 84131131 84131131 CCCCCGCCTGGGGAGCAGAGCAGACTTGATCAAGCAGTATGGAAGATGGGCCGTTGTCAGCGGTA CCCCCGCCTGGGGAGCAGAGCAGACTTGATCAGGCAGTATGGAAGATGGGCCGTTGTCAGCGGTA T C HSDL1 Ensembl:ENSG00000103160 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs776607024 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1523502,Human_RBP_ID_5572094,Human_RBP_ID_6542559 Human_Splice_Rec_1745459,Human_Splice_Rec_1745471,Human_Splice_Rec_1745483,Human_Splice_Rec_1745489 RMVar_hsa_circ_307631,RMVar_hsa_circ_338523,RMVar_hsa_circ_180291,RMVar_hsa_circ_180292 22754 RMVar_ID_22754 Human_SNP_ID_612095770 A-to-I Human chr16 - 84131653 84131653 84131653 AAAATTAGCCGGGCGTGGTGGCATGTGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA AAAATTAGCCGGGCGTGGTGGCATGTGCCTGTGGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA T C HSDL1 Ensembl:ENSG00000103160 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1293943623 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_126396 RMVar_hsa_circ_307631,RMVar_hsa_circ_180292 22755 RMVar_ID_22755 Human_SNP_ID_612105071 A-to-I Human chr16 + 84157313 84157313 84157313 GGGAGGCCCAGGTGGGCAGGTCACTTGAGGCCAGGAGTTTGAGACCAGCCTGGTCAACATGGCAA GGGAGGCCCAGGTGGGCAGGTCACTTGAGGCCGGGAGTTTGAGACCAGCCTGGTCAACATGGCAA A G DNAAF1 Ensembl:ENSG00000154099 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs558627022 Functional Loss SNV dbSNP153 33..33 33 - - - 22756 RMVar_ID_22756 Human_SNP_ID_612105080 A-to-I Human chr16 + 84157358 84157358 84157358 CAGCCTGGTCAACATGGCAAAACCCCATCTCTACTAACAATACAAAAATTAGCTGGGCATGGTGG CAGCCTGGTCAACATGGCAAAACCCCATCTCTGCTAACAATACAAAAATTAGCTGGGCATGGTGG A G DNAAF1 Ensembl:ENSG00000154099 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs536341718 Functional Loss SNV dbSNP153 33..33 33 - - - 22757 RMVar_ID_22757 Human_SNP_ID_612105084 A-to-I Human chr16 + 84157371 84157371 84157371 ATGGCAAAACCCCATCTCTACTAACAATACAAAAATTAGCTGGGCATGGTGGTGCACGTCTGTGA ATGGCAAAACCCCATCTCTACTAACAATACAACAATTAGCTGGGCATGGTGGTGCACGTCTGTGA A C DNAAF1 Ensembl:ENSG00000154099 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1362527571 Functional Loss SNV dbSNP153 33..33 33 - - - 22758 RMVar_ID_22758 Human_SNP_ID_612113102 A-to-I Human chr16 - 84179222 84179222 84179222 TGGATCCCTCAGAGGACACCAGCTCCCCTCATAGCCCTGAGTGGCCACCTGCTGATGCTCTGCCC TGGATCCCTCAGAGGACACCAGCTCCCCTCATGGCCCTGAGTGGCCACCTGCTGATGCTCTGCCC T C TAF1C Ensembl:ENSG00000103168 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1307506324 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_480630,Human_RBP_ID_22206199 Human_Splice_Rec_1745742 Human_miRNA_ID_598240,Human_miRNA_ID_829149,Human_miRNA_ID_1045148,Human_miRNA_ID_1347435 22759 RMVar_ID_22759 Human_SNP_ID_612169172 A-to-I Human chr16 + 84327098 84327098 84327098 TACTGGTAGAATTTGAAATTCCCTTCTGCAGTAAGTCCTCACCTAACGTCATCAATAGGTTCTTG TACTGGTAGAATTTGAAATTCCCTTCTGCAGTGAGTCCTCACCTAACGTCATCAATAGGTTCTTG A G WFDC1 Ensembl:ENSG00000103175 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1461177286 Functional Loss SNV dbSNP153 33..33 33 - - - 22760 RMVar_ID_22760 Human_SNP_ID_612239364 A-to-I Human chr16 - 84499921 84499921 84499921 GCGATCCTCCCGCCTCAGCCTTTGGAGCAGCTAGGACTGTAAGCACATACCACCGTGCCTGGCGA GCGATCCTCCCGCCTCAGCCTTTGGAGCAGCTGGGACTGTAAGCACATACCACCGTGCCTGGCGA T C MEAK7 Ensembl:ENSG00000140950 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1261210513 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1746389 22761 RMVar_ID_22761 Human_SNP_ID_612239407 A-to-I Human chr16 - 84499993 84499993 84499993 TTGCCCTTTTACCCAGGCTGGAGTGCAGTGGCACGATCATAGCTCACTGCAGCCTTGACGTCCTG TTGCCCTTTTACCCAGGCTGGAGTGCAGTGGCGCGATCATAGCTCACTGCAGCCTTGACGTCCTG T C MEAK7 Ensembl:ENSG00000140950 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs954224125 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1746388,Human_Splice_Rec_1746389 22762 RMVar_ID_22762 Human_SNP_ID_612266370 A-to-I Human chr16 - 84573701 84573701 84573701 AGTTTCGCTCTTGTCACCCAGGCTGGAGTGCAATGGTGCGATCTAAGCTCACTGCAACTTCCGCC AGTTTCGCTCTTGTCACCCAGGCTGGAGTGCAGTGGTGCGATCTAAGCTCACTGCAACTTCCGCC T C COTL1 Ensembl:ENSG00000103187 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1295036307 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77935,RMVar_hsa_circ_108047,RMVar_hsa_circ_82122,RMVar_hsa_circ_180313,RMVar_hsa_circ_180314,RMVar_hsa_circ_180315 22763 RMVar_ID_22763 Human_SNP_ID_612312396 A-to-I Human chr16 + 84707914 84707914 84707914 CAGCCTGGGCAACGTAGCAAAACTCTTTCTCTACAAAAATACAAAAATTCACTGGGCATGGTGGT CAGCCTGGGCAACGTAGCAAAACTCTTTCTCTGCAAAAATACAAAAATTCACTGGGCATGGTGGT A G USP10 Ensembl:ENSG00000103194 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1007383095 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12829615,Human_RBP_ID_17002958 RMVar_hsa_circ_348782 22764 RMVar_ID_22764 Human_SNP_ID_612312411 A-to-I Human chr16 + 84707967 84707967 84707967 GGGCATGGTGGTGCTCTCCTGTAGTCCCACCTACTTGGGAGGTTGAGGTGGGAGGATCGCTTGAA GGGCATGGTGGTGCTCTCCTGTAGTCCCACCTGCTTGGGAGGTTGAGGTGGGAGGATCGCTTGAA A G USP10 Ensembl:ENSG00000103194 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs918990329 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_348782 22765 RMVar_ID_22765 Human_SNP_ID_612313090 A-to-I Human chr16 + 84710023 84710023 84710023 CCGGGTGCGAGGCTCACGCCTGTAATCCCAGCACTTTGGGAGACCGAAGTAGACGGATCACTTGA CCGGGTGCGAGGCTCACGCCTGTAATCCCAGCCCTTTGGGAGACCGAAGTAGACGGATCACTTGA A C USP10 Ensembl:ENSG00000103194 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1377202652 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_348782 22766 RMVar_ID_22766 Human_SNP_ID_612313118 A-to-I Human chr16 + 84710099 84710099 84710099 TGAGACCAGTCTGGCCAACATGCTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCCGGGCG TGAGACCAGTCTGGCCAACATGCTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCCGGGCG A G USP10 Ensembl:ENSG00000103194 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1367548954 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_348782 22767 RMVar_ID_22767 Human_SNP_ID_612327841 A-to-I Human chr16 + 84750348 84750345 84750348 GAGAATAGCTTGAACCGGGGAGGTGGAGGTTCAGTGAGCCCAGATCGTGCCACTGCACTCCAGCC GAGAATAGCTTGAACCGGGGAGGTGGAGGT___GTGAGCCCAGATCGTGCCACTGCACTCCAGCC TTCA T USP10 Ensembl:ENSG00000103194 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1332286564 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_25234401 RMVar_hsa_circ_108263,RMVar_hsa_circ_348800,RMVar_hsa_circ_180324,RMVar_hsa_circ_339590,RMVar_hsa_circ_180321,RMVar_hsa_circ_180322,RMVar_hsa_circ_370478,RMVar_hsa_circ_273393,RMVar_hsa_circ_180325 22768 RMVar_ID_22768 Human_SNP_ID_612335302 A-to-I Human chr16 + 84770818 84770818 84770818 AAAAATCTCCAGTGGCTGATGCCTGTAATCCCAGCATTTTCGGAGGCTGAGGCAGGCGGATCACA AAAAATCTCCAGTGGCTGATGCCTGTAATCCCCGCATTTTCGGAGGCTGAGGCAGGCGGATCACA A C USP10 Ensembl:ENSG00000103194 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs536506356 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108263,RMVar_hsa_circ_180322,RMVar_hsa_circ_315112,RMVar_hsa_circ_20744,RMVar_hsa_circ_180326,RMVar_hsa_circ_100565,RMVar_hsa_circ_180330,RMVar_hsa_circ_313234,RMVar_hsa_circ_180331 22769 RMVar_ID_22769 Human_SNP_ID_612335303 A-to-I Human chr16 + 84770818 84770818 84770818 AAAAATCTCCAGTGGCTGATGCCTGTAATCCCAGCATTTTCGGAGGCTGAGGCAGGCGGATCACA AAAAATCTCCAGTGGCTGATGCCTGTAATCCCGGCATTTTCGGAGGCTGAGGCAGGCGGATCACA A G USP10 Ensembl:ENSG00000103194 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs536506356 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108263,RMVar_hsa_circ_180322,RMVar_hsa_circ_315112,RMVar_hsa_circ_20744,RMVar_hsa_circ_180326,RMVar_hsa_circ_100565,RMVar_hsa_circ_180330,RMVar_hsa_circ_313234,RMVar_hsa_circ_180331 22770 RMVar_ID_22770 Human_SNP_ID_612336741 A-to-I Human chr16 + 84774677 84774677 84774677 TATTTTTAATAGAGACGTGGTTTCACTGTATTAGCCAGGATGGTCTCGATCTCCTGACCTCGTGA TATTTTTAATAGAGACGTGGTTTCACTGTATTGGCCAGGATGGTCTCGATCTCCTGACCTCGTGA A G USP10 Ensembl:ENSG00000103194 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1387177893 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108263,RMVar_hsa_circ_180322,RMVar_hsa_circ_315112,RMVar_hsa_circ_180326,RMVar_hsa_circ_100565,RMVar_hsa_circ_180330,RMVar_hsa_circ_313234,RMVar_hsa_circ_180331,RMVar_hsa_circ_180332,RMVar_hsa_circ_314617 22771 RMVar_ID_22771 Human_SNP_ID_612409993 A-to-I Human chr16 - 84982276 84982276 84982276 CAACGGCGCGATCTTGGCTCACTGCAACCTCTACCTCCTGAGTTCAAGCGATTCTCCTGCCTCAG CAACGGCGCGATCTTGGCTCACTGCAACCTCTGCCTCCTGAGTTCAAGCGATTCTCCTGCCTCAG T C ZDHHC7 Ensembl:ENSG00000153786 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1013901276 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51794,RMVar_hsa_circ_180348,RMVar_hsa_circ_321191,RMVar_hsa_circ_180347 22772 RMVar_ID_22772 Human_SNP_ID_612410496 A-to-I Human chr16 - 84983851 84983851 84983851 ATATTACAAGCGCAGGCCACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCGC ATATTACAAGCGCAGGCCACCACGCCCAGCTATTTTTTGTATTTTTAGTAGAGATGGGGTTTCGC T A ZDHHC7 Ensembl:ENSG00000153786 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1408137272 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51794,RMVar_hsa_circ_180348,RMVar_hsa_circ_321191,RMVar_hsa_circ_180347 22773 RMVar_ID_22773 Human_SNP_ID_612410498 A-to-I Human chr16 - 84983856 84983856 84983856 CTGGGATATTACAAGCGCAGGCCACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGT CTGGGATATTACAAGCGCAGGCCACCACGCCCGGCTAATTTTTGTATTTTTAGTAGAGATGGGGT T C ZDHHC7 Ensembl:ENSG00000153786 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1303985864 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51794,RMVar_hsa_circ_180348,RMVar_hsa_circ_321191,RMVar_hsa_circ_180347 22774 RMVar_ID_22774 Human_SNP_ID_612413284 A-to-I Human chr16 - 84992019 84992019 84992019 GGCGCACGCCACCATGCCCGGCTGGTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGA GGCGCACGCCACCATGCCCGGCTGGTTTTTGTGTTTTTAGTAGAGACGGGGTTTCACCATGTTGA T C ZDHHC7 Ensembl:ENSG00000153786 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1455796109 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97665,RMVar_hsa_circ_51794,RMVar_hsa_circ_180348,RMVar_hsa_circ_321191,RMVar_hsa_circ_180350,RMVar_hsa_circ_296860,RMVar_hsa_circ_180349 22775 RMVar_ID_22775 Human_SNP_ID_612415530 A-to-I Human chr16 - 84998152 84998152 84998152 TCGCGCCGTTCTCCTGTCTCAGCCTCCCGAGTAGCTGGGACTGCAGGCGCCCGCCACCACGCCCG TCGCGCCGTTCTCCTGTCTCAGCCTCCCGAGTTGCTGGGACTGCAGGCGCCCGCCACCACGCCCG T A ZDHHC7 Ensembl:ENSG00000153786 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1216831712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_128680 22776 RMVar_ID_22776 Human_SNP_ID_612430631 A-to-I Human chr16 + 85042388 85042388 85042388 CGAGGGAGTATTAATCCACCCCGGTGTACTGCAGCTATGTAAAGGGTCCTTATTCATCCCCCAGA CGAGGGAGTATTAATCCACCCCGGTGTACTGCCGCTATGTAAAGGGTCCTTATTCATCCCCCAGA A C KIAA0513 Ensembl:ENSG00000135709 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1179789455 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98786,RMVar_hsa_circ_180352 22777 RMVar_ID_22777 Human_SNP_ID_612440264 A-to-I Human chr16 + 85070491 85070491 85070491 CCTAAGGCCAGGAGTTTGAGACCAGCCTGGCCAACATGATGAAACCCCGTCTCTACTAAAAACAC CCTAAGGCCAGGAGTTTGAGACCAGCCTGGCCGACATGATGAAACCCCGTCTCTACTAAAAACAC A G KIAA0513 Ensembl:ENSG00000135709 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1325885548 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42651,RMVar_hsa_circ_29206 22778 RMVar_ID_22778 Human_SNP_ID_612440266 A-to-I Human chr16 + 85070497 85070497 85070497 GCCAGGAGTTTGAGACCAGCCTGGCCAACATGATGAAACCCCGTCTCTACTAAAAACACAAAAAT GCCAGGAGTTTGAGACCAGCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAACACAAAAAT A G KIAA0513 Ensembl:ENSG00000135709 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1391378188 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42651,RMVar_hsa_circ_29206 22779 RMVar_ID_22779 Human_SNP_ID_612440289 A-to-I Human chr16 + 85070547 85070547 85070547 TAAAAACACAAAAATTAGCTGGGCGTGGTGGCAGGTGCCTGTAATCCCTGCTACTCGGGAGGCTG TAAAAACACAAAAATTAGCTGGGCGTGGTGGCGGGTGCCTGTAATCCCTGCTACTCGGGAGGCTG A G KIAA0513 Ensembl:ENSG00000135709 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1321650290 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42651,RMVar_hsa_circ_29206 22780 RMVar_ID_22780 Human_SNP_ID_612440300 A-to-I Human chr16 + 85070567 85070567 85070567 GGGCGTGGTGGCAGGTGCCTGTAATCCCTGCTACTCGGGAGGCTGAGGCAGGAAAATCACTTGAA GGGCGTGGTGGCAGGTGCCTGTAATCCCTGCTGCTCGGGAGGCTGAGGCAGGAAAATCACTTGAA A G KIAA0513 Ensembl:ENSG00000135709 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1446264695 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42651,RMVar_hsa_circ_29206 22781 RMVar_ID_22781 Human_SNP_ID_612466905 A-to-I Human chr16 + 85148679 85148679 85148679 TCTGACCCACACAGCGAAACCCCGTCTCTACTAAAAATACAAAAAATCAGCTGGGCGTGGTGGTG TCTGACCCACACAGCGAAACCCCGTCTCTACTGAAAATACAAAAAATCAGCTGGGCGTGGTGGTG A G LINC02139 Ensembl:ENSG00000278214 lincRNA exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs536688614 Functional Loss SNV dbSNP153 33..33 33 - - - 22782 RMVar_ID_22782 Human_SNP_ID_612559638 A-to-I Human chr16 + 85415140 85415140 85415140 TTTTGTATTTTCTGTAGAGACAGGGTCTCCCTATGTTGCCCAGACTGGTCTTGAACCCCCGTACT TTTTGTATTTTCTGTAGAGACAGGGTCTCCCTGTGTTGCCCAGACTGGTCTTGAACCCCCGTACT A G GSE1 Ensembl:ENSG00000131149 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1043845375 Functional Loss SNV dbSNP153 33..33 33 - - - 22783 RMVar_ID_22783 Human_SNP_ID_612559639 A-to-I Human chr16 + 85415140 85415140 85415140 TTTTGTATTTTCTGTAGAGACAGGGTCTCCCTATGTTGCCCAGACTGGTCTTGAACCCCCGTACT TTTTGTATTTTCTGTAGAGACAGGGTCTCCCTTTGTTGCCCAGACTGGTCTTGAACCCCCGTACT A T GSE1 Ensembl:ENSG00000131149 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1043845375 Functional Loss SNV dbSNP153 33..33 33 - - - 22784 RMVar_ID_22784 Human_SNP_ID_612560266 A-to-I Human chr16 + 85417053 85417053 85417053 ATTTTTTTGTATTTTTTTGTAGAGCAGGTCTCACCATGTTGCCCAGGCTGGTCTCAAACTTATGG ATTTTTTTGTATTTTTTTGTAGAGCAGGTCTCTCCATGTTGCCCAGGCTGGTCTCAAACTTATGG A T GSE1 Ensembl:ENSG00000131149 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs937455336 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23704313 22785 RMVar_ID_22785 Human_SNP_ID_612576967 A-to-I Human chr16 + 85468574 85468574 85468574 TCCTGACCTCCTGTGATCCACCAGCCCCCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG TCCTGACCTCCTGTGATCCACCAGCCCCCCTCCGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG A C GSE1 Ensembl:ENSG00000131149 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1034193968 Functional Loss SNV dbSNP153 33..33 33 - - - 22786 RMVar_ID_22786 Human_SNP_ID_612580531 A-to-I Human chr16 + 85478737 85478737 85478737 TCGCCCAGGCTGGAGTGCAGTGGCTCCATCTCAGCTCACTGCAACCTCTGCCTCCCAAGTTCAAG TCGCCCAGGCTGGAGTGCAGTGGCTCCATCTCGGCTCACTGCAACCTCTGCCTCCCAAGTTCAAG A G GSE1 Ensembl:ENSG00000131149 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1403194398 Functional Loss SNV dbSNP153 33..33 33 - - - 22787 RMVar_ID_22787 Human_SNP_ID_612610918 A-to-I Human chr16 + 85567913 85567912 85567914 CCTGGCTAATTTTTAAATTTTTTTGTAGAGACAGAGTCTTCTTATGTTGCCCAGGCTGATCTCGC CCTGGCTAATTTTTAAATTTTTTTGTAGAGAC__AGTCTTCTTATGTTGCCCAGGCTGATCTCGC CAG C GSE1 Ensembl:ENSG00000131149 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs375233150 Functional Loss DEL dbSNP153 33..34 33 - - - 22788 RMVar_ID_22788 Human_SNP_ID_612648882 A-to-I Human chr16 + 85660815 85660815 85660815 ACCATGCCTGGCTAATTTTTGTATTTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGG ACCATGCCTGGCTAATTTTTGTATTTTTTAGTGGAGATGGGGTTTCACCATGTTGGCCAGGCTGG A G GSE1 Ensembl:ENSG00000131149 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1191452426 Functional Loss SNV dbSNP153 33..33 33 - - - 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 22789 RMVar_ID_22789 Human_SNP_ID_612654568 A-to-I Human chr16 + 85672030 85672030 85672030 GGACTTTGTTTCTCTTTTTGAGGCGAAGTCTCACTCTGTCACCCAAGCTGGAATGCAGTGGCGCA GGACTTTGTTTCTCTTTTTGAGGCGAAGTCTCCCTCTGTCACCCAAGCTGGAATGCAGTGGCGCA A C GSE1 Ensembl:ENSG00000131149 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs953642432 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8440780 22790 RMVar_ID_22790 Human_SNP_ID_612657025 A-to-I Human chr16 - 85676769 85676768 85676770 CTCACTGCAGCCTCGAACTCCTGGGTTCACACAGTTCTCCCACCACAGCCTCCCAAAGCACTGGG CTCACTGCAGCCTCGAACTCCTGGGTTCACA__GTTCTCCCACCACAGCCTCCCAAAGCACTGGG CTG C GINS2 Ensembl:ENSG00000131153 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1363955302 Functional Loss DEL dbSNP153 32..33 33 - - - 22791 RMVar_ID_22791 Human_SNP_ID_612657086 A-to-I Human chr16 - 85676932 85676932 85676932 TGAACCCGAGAGGCGGAGGTTGTAGTGAGCCAAGATTGCACCACTGTACTCCTGCCTGGGCAACG TGAACCCGAGAGGCGGAGGTTGTAGTGAGCCACGATTGCACCACTGTACTCCTGCCTGGGCAACG T G GINS2 Ensembl:ENSG00000131153 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1325880912 Functional Loss SNV dbSNP153 33..33 33 - - - 22792 RMVar_ID_22792 Human_SNP_ID_612684210 A-to-I Human chr16 - 85749060 85749060 85749060 AGTGATGATGGGGCCCAGGCACAGTGGCTCACACCTGTGATCCCAGTGCTTTGGGAGGGTGAGGC AGTGATGATGGGGCCCAGGCACAGTGGCTCACCCCTGTGATCCCAGTGCTTTGGGAGGGTGAGGC T G C16orf74 Ensembl:ENSG00000154102 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1026825085 Functional Loss SNV dbSNP153 33..33 33 - - - 22793 RMVar_ID_22793 Human_SNP_ID_612691646 A-to-I Human chr16 - 85771520 85771520 85771520 ACAATCTTGGCTTACCACAAACTCTGCCTCCCAGGTTCAAGCTATTCTCCTGCCTCAGCCTTCCA ACAATCTTGGCTTACCACAAACTCTGCCTCCCGGGTTCAAGCTATTCTCCTGCCTCAGCCTTCCA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1387894761 Functional Loss SNV dbSNP153 33..33 33 - - - 22794 RMVar_ID_22794 Human_SNP_ID_612695845 A-to-I Human chr16 - 85783644 85783644 85783644 TTGAAGACACAGCATTGCCCCTGTGGCTGCACACGGTAGCTCAGTTCACCGTAACGAAGGCCTGC TTGAAGACACAGCATTGCCCCTGTGGCTGCACGCGGTAGCTCAGTTCACCGTAACGAAGGCCTGC T C EMC8 Ensembl:ENSG00000131148 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs301171 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2108,GWAS_ID_2109,GWAS_ID_2110 RMVar_hsa_circ_115833,RMVar_hsa_circ_180377 22795 RMVar_ID_22795 Human_SNP_ID_612696352 A-to-I Human chr16 - 85785117 85785117 85785117 ATAGCAAGACCTCATCTCTACAAAAAAATACAAAAATTAGCTGGACATGGTGGCCTACGCCTGTG ATAGCAAGACCTCATCTCTACAAAAAAATACAGAAATTAGCTGGACATGGTGGCCTACGCCTGTG T C EMC8 Ensembl:ENSG00000131148 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs373977148 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115833,RMVar_hsa_circ_180377 22796 RMVar_ID_22796 Human_SNP_ID_612700312 A-to-I Human chr16 - 85797190 85797190 85797190 TTGACCAGGCTGGTCTTGAACTCCTTACCTCAAGTAATACGGCCACCTCCGCATCCCAAAGTGCT TTGACCAGGCTGGTCTTGAACTCCTTACCTCATGTAATACGGCCACCTCCGCATCCCAAAGTGCT T A EMC8 Ensembl:ENSG00000131148 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049089395 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115833,RMVar_hsa_circ_180377 22797 RMVar_ID_22797 Human_SNP_ID_612700313 A-to-I Human chr16 - 85797190 85797190 85797190 TTGACCAGGCTGGTCTTGAACTCCTTACCTCAAGTAATACGGCCACCTCCGCATCCCAAAGTGCT TTGACCAGGCTGGTCTTGAACTCCTTACCTCAGGTAATACGGCCACCTCCGCATCCCAAAGTGCT T C EMC8 Ensembl:ENSG00000131148 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049089395 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115833,RMVar_hsa_circ_180377 22798 RMVar_ID_22798 Human_SNP_ID_612700373 A-to-I Human chr16 - 85797364 85797364 85797364 CGCTCTTGTCACCCAGCCTGGAGTGCAATGGCATGATCTCGGCTCACTGCAACTTCCACCTCCCA CGCTCTTGTCACCCAGCCTGGAGTGCAATGGCGTGATCTCGGCTCACTGCAACTTCCACCTCCCA T C EMC8 Ensembl:ENSG00000131148 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1567835714 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115833,RMVar_hsa_circ_180377 22799 RMVar_ID_22799 Human_SNP_ID_612969873 A-to-I Human chr16 - 86534477 86534477 86534477 TTCTCATTCTTCCCCTCCCATCTGTGTCCAGTAGCACCTCAAGCTTCCCTATGGCAGAAGCAAGC TTCTCATTCTTCCCCTCCCATCTGTGTCCAGTGGCACCTCAAGCTTCCCTATGGCAGAAGCAAGC T C MTHFSD Ensembl:ENSG00000103248 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs772982746 Functional Loss SNV dbSNP153 33..33 33 - - - 22800 RMVar_ID_22800 Human_SNP_ID_612970037 A-to-I Human chr16 - 86535023 86535022 86535026 CCACGGCATGTTTCAAAACAGATTTCTGCCGCAGAACCCCAAGTGTGAAGCCTCGCCTGAGAATG CCACGGCATGTTTCAAAACAGATTTCTGCTGCAAAACCCCAAGTGTGAAGCCTCGCCTGAGAATG CTGCG TTGCA MTHFSD Ensembl:ENSG00000103248 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs386793715 Functional Loss MNV dbSNP153 30..34 33 - - - 22801 RMVar_ID_22801 Human_SNP_ID_612970059 A-to-I Human chr16 - 86535073 86535073 86535073 AGAATAAAGGAGCTCCCTGTGATGTGCACGGAAGGATATATTTGTCTTTCCCACGGCATGTTTCA AGAATAAAGGAGCTCCCTGTGATGTGCACGGACGGATATATTTGTCTTTCCCACGGCATGTTTCA T G MTHFSD Ensembl:ENSG00000103248 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1011000328 Functional Loss SNV dbSNP153 33..33 33 - - - 22802 RMVar_ID_22802 Human_SNP_ID_612970068 A-to-I Human chr16 - 86535102 86535102 86535102 TCTTCAGCCGATTGTATATTTGCTGGCTCAGAATAAAGGAGCTCCCTGTGATGTGCACGGAAGGA TCTTCAGCCGATTGTATATTTGCTGGCTCAGAGTAAAGGAGCTCCCTGTGATGTGCACGGAAGGA T C MTHFSD Ensembl:ENSG00000103248 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs966187014 Functional Loss SNV dbSNP153 33..33 33 - - - 22803 RMVar_ID_22803 Human_SNP_ID_613253624 A-to-I Human chr16 - 87357529 87357529 87357529 GAGGTCAGGAGTTCGAGACCTGTCTGGCCAACATGGTGAAACTCATCTCTACTAAAAGTACAAAA GAGGTCAGGAGTTCGAGACCTGTCTGGCCAACTTGGTGAAACTCATCTCTACTAAAAGTACAAAA T A FBXO31 Ensembl:ENSG00000103264 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1567478945 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17564419 RMVar_hsa_circ_116890,RMVar_hsa_circ_180400,RMVar_hsa_circ_180405,RMVar_hsa_circ_303514 22804 RMVar_ID_22804 Human_SNP_ID_613253626 A-to-I Human chr16 - 87357531 87357531 87357531 CTGAGGTCAGGAGTTCGAGACCTGTCTGGCCAACATGGTGAAACTCATCTCTACTAAAAGTACAA CTGAGGTCAGGAGTTCGAGACCTGTCTGGCCATCATGGTGAAACTCATCTCTACTAAAAGTACAA T A FBXO31 Ensembl:ENSG00000103264 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs560529666 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17564419 RMVar_hsa_circ_116890,RMVar_hsa_circ_180400,RMVar_hsa_circ_180405,RMVar_hsa_circ_303514 22805 RMVar_ID_22805 Human_SNP_ID_613253627 A-to-I Human chr16 - 87357531 87357531 87357531 CTGAGGTCAGGAGTTCGAGACCTGTCTGGCCAACATGGTGAAACTCATCTCTACTAAAAGTACAA CTGAGGTCAGGAGTTCGAGACCTGTCTGGCCAGCATGGTGAAACTCATCTCTACTAAAAGTACAA T C FBXO31 Ensembl:ENSG00000103264 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs560529666 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17564419 RMVar_hsa_circ_116890,RMVar_hsa_circ_180400,RMVar_hsa_circ_180405,RMVar_hsa_circ_303514 22806 RMVar_ID_22806 Human_SNP_ID_613253648 A-to-I Human chr16 - 87357595 87357595 87357595 GGCCAGACATGGTGGCTAATGCCTGTAATCCCAGTGCTTTGGGAGGCCGAGGCAGGTGGATCATC GGCCAGACATGGTGGCTAATGCCTGTAATCCCGGTGCTTTGGGAGGCCGAGGCAGGTGGATCATC T C FBXO31 Ensembl:ENSG00000103264 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs976573176 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12868534,Human_RBP_ID_17564420 RMVar_hsa_circ_116890,RMVar_hsa_circ_180400,RMVar_hsa_circ_180405,RMVar_hsa_circ_303514 22807 RMVar_ID_22807 Human_SNP_ID_613255153 A-to-I Human chr16 - 87362395 87362395 87362395 ATAGTGGGACATGAGACTCCATTTCTAAATAAATAAATGTATGTATGTATGTATGTTTTACCTGT ATAGTGGGACATGAGACTCCATTTCTAAATAAGTAAATGTATGTATGTATGTATGTTTTACCTGT T C FBXO31 Ensembl:ENSG00000103264 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs548224245 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2488494,Human_RBP_ID_3501048,Human_RBP_ID_8441055,Human_RBP_ID_12880581,Human_RBP_ID_23705225 RMVar_hsa_circ_180407 22808 RMVar_ID_22808 Human_SNP_ID_613255252 A-to-I Human chr16 - 87362689 87362689 87362689 CAGCATGGTGTTGTGTGCCTGTAGGCCCAGCTACTCAGGAGGGTGAGGCAGGAGAATCGCTTGAA CAGCATGGTGTTGTGTGCCTGTAGGCCCAGCTGCTCAGGAGGGTGAGGCAGGAGAATCGCTTGAA T C FBXO31 Ensembl:ENSG00000103264 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs546047354 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_180407 22809 RMVar_ID_22809 Human_SNP_ID_613255267 A-to-I Human chr16 - 87362740 87362740 87362740 CCAACATGGTGAATTAAAACCCCATCTCTACTAAAAATACAAAAATTGGCCCAGCATGGTGTTGT CCAACATGGTGAATTAAAACCCCATCTCTACTGAAAATACAAAAATTGGCCCAGCATGGTGTTGT T C FBXO31 Ensembl:ENSG00000103264 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285424025 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_180407 22810 RMVar_ID_22810 Human_SNP_ID_613255291 A-to-I Human chr16 - 87362829 87362829 87362829 ACTCTGGCCATGCACAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAGATCACTTGTG ACTCTGGCCATGCACAGTGGCTCACGCCTGTATTCCCAGCACTTTGGGAGGCCAGATCACTTGTG T A FBXO31 Ensembl:ENSG00000103264 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1204315242 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_180407 22811 RMVar_ID_22811 Human_SNP_ID_613255299 A-to-I Human chr16 - 87362846 87362846 87362846 GATAAATAAATGTTTAAACTCTGGCCATGCACAGTGGCTCACGCCTGTAATCCCAGCACTTTGGG GATAAATAAATGTTTAAACTCTGGCCATGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG T C FBXO31 Ensembl:ENSG00000103264 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs544790110 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_180407 22812 RMVar_ID_22812 Human_SNP_ID_613258682 A-to-I Human chr16 - 87372875 87372875 87372875 CAAAAATTAGTGGGGTGTGGTGGCGTGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGAAGA CAAAAATTAGTGGGGTGTGGTGGCGTGCCTGTGGTCCCAGCTACTTGGGAGGCTGAGGCAGAAGA T C FBXO31 Ensembl:ENSG00000103264 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1209738233 Functional Loss SNV dbSNP153 33..33 33 - - - 22813 RMVar_ID_22813 Human_SNP_ID_613259113 A-to-I Human chr16 - 87374130 87374130 87374130 TCGAGGAATCCTCCTGCCTTAGCCTCTCAAGTAGTTGGGACTGTAGGCATGTGCCACCACACCTG TCGAGGAATCCTCCTGCCTTAGCCTCTCAAGTGGTTGGGACTGTAGGCATGTGCCACCACACCTG T C FBXO31 Ensembl:ENSG00000103264 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1362485739 Functional Loss SNV dbSNP153 33..33 33 - - - 22814 RMVar_ID_22814 Human_SNP_ID_613261380 A-to-I Human chr16 - 87380549 87380549 87380549 ACCCATCTCTACAAAAAATACAAAAGTTAGCCAGTCATGGTGGTGCGTGCCTGTGGAAGGCTGAG ACCCATCTCTACAAAAAATACAAAAGTTAGCCTGTCATGGTGGTGCGTGCCTGTGGAAGGCTGAG T A FBXO31 Ensembl:ENSG00000103264 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1415584181 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17564426 22815 RMVar_ID_22815 Human_SNP_ID_613267333 A-to-I Human chr16 + 87396876 87396876 87396876 TGAGACAAAAGTCTTGCTCTGTCGCCCAGACTAGAGTGCAGTGGCGTGATCTCGGCTGACTGCAA TGAGACAAAAGTCTTGCTCTGTCGCCCAGACTGGAGTGCAGTGGCGTGATCTCGGCTGACTGCAA A G MAP1LC3B Ensembl:ENSG00000140941 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs953894343 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_180409,RMVar_hsa_circ_92987 22816 RMVar_ID_22816 Human_SNP_ID_613267539 A-to-I Human chr16 + 87397503 87397503 87397503 AGCCGAGCATGGTGTCGGGTGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGTG AGCCGAGCATGGTGTCGGGTGCCTGTAGTCCCCGCTACTCGGGAGGCTGAGGCAGGAGAATGGTG A C MAP1LC3B Ensembl:ENSG00000140941 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs969706562 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_180409,RMVar_hsa_circ_92987 22817 RMVar_ID_22817 Human_SNP_ID_613270067 A-to-I Human chr16 + 87404639 87404635 87404639 AACTACCGTGTGATCAGTAAGATTCCTGTAAGAAATACTGCTTTTTAAGAAAAAAAATAACATGC AACTACCGTGTGATCAGTAAGATTCCTGT____AATACTGCTTTTTAAGAAAAAAAATAACATGC TAAGA T MAP1LC3B Ensembl:ENSG00000140941 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1375628444 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_481182,Human_RBP_ID_1523993,Human_RBP_ID_1847556,Human_RBP_ID_5113673,Human_RBP_ID_8947613,Human_RBP_ID_9066313,Human_RBP_ID_12836989,Human_RBP_ID_17256196,Human_RBP_ID_18288143,Human_RBP_ID_21889470,Human_RBP_ID_23705280,Human_RBP_ID_24477189 RMVar_hsa_circ_180409,RMVar_hsa_circ_92987 22818 RMVar_ID_22818 Human_SNP_ID_613270069 A-to-I Human chr16 + 87404639 87404639 87404639 AACTACCGTGTGATCAGTAAGATTCCTGTAAGAAATACTGCTTTTTAAGAAAAAAAATAACATGC AACTACCGTGTGATCAGTAAGATTCCTGTAAGGAATACTGCTTTTTAAGAAAAAAAATAACATGC A G MAP1LC3B Ensembl:ENSG00000140941 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs921185909 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_481182,Human_RBP_ID_1523993,Human_RBP_ID_1847556,Human_RBP_ID_5113673,Human_RBP_ID_8947613,Human_RBP_ID_9066313,Human_RBP_ID_12836989,Human_RBP_ID_17256196,Human_RBP_ID_18288143,Human_RBP_ID_21889470,Human_RBP_ID_23705280,Human_RBP_ID_24477189 RMVar_hsa_circ_180409,RMVar_hsa_circ_92987 22819 RMVar_ID_22819 Human_SNP_ID_613388097 A-to-I Human chr16 - 87728013 87728013 87728013 TTGGCTAATTTTTTGTGTTTTTAGTAGAGACAAGGTTTCACCATATTGTCCAGGCTGTTTTTGAA TTGGCTAATTTTTTGTGTTTTTAGTAGAGACAGGGTTTCACCATATTGTCCAGGCTGTTTTTGAA T C KLHDC4 Ensembl:ENSG00000104731 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1171703707 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12838599 RMVar_hsa_circ_8657,RMVar_hsa_circ_300861,RMVar_hsa_circ_112074,RMVar_hsa_circ_15052,RMVar_hsa_circ_92030,RMVar_hsa_circ_11021,RMVar_hsa_circ_39413,RMVar_hsa_circ_180432,RMVar_hsa_circ_180433,RMVar_hsa_circ_26160,RMVar_hsa_circ_319135,RMVar_hsa_circ_281186,RMVar_hsa_circ_293219,RMVar_hsa_circ_353127,RMVar_hsa_circ_110926,RMVar_hsa_circ_180435,RMVar_hsa_circ_180436,RMVar_hsa_circ_180434 22820 RMVar_ID_22820 Human_SNP_ID_613388165 A-to-I Human chr16 - 87728171 87728171 87728171 TTTTCTTTCTTCTTTTTTTGAGACAGATTCTCACTCGATCGCCCAGGCTGGAGTGCAGTGGCGTG TTTTCTTTCTTCTTTTTTTGAGACAGATTCTCCCTCGATCGCCCAGGCTGGAGTGCAGTGGCGTG T G KLHDC4 Ensembl:ENSG00000104731 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1213513934 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12838605 RMVar_hsa_circ_8657,RMVar_hsa_circ_300861,RMVar_hsa_circ_112074,RMVar_hsa_circ_15052,RMVar_hsa_circ_92030,RMVar_hsa_circ_11021,RMVar_hsa_circ_39413,RMVar_hsa_circ_180432,RMVar_hsa_circ_180433,RMVar_hsa_circ_26160,RMVar_hsa_circ_319135,RMVar_hsa_circ_281186,RMVar_hsa_circ_293219,RMVar_hsa_circ_353127,RMVar_hsa_circ_110926,RMVar_hsa_circ_180435,RMVar_hsa_circ_180436,RMVar_hsa_circ_180434 22821 RMVar_ID_22821 Human_SNP_ID_613388424 A-to-I Human chr16 - 87728831 87728831 87728831 GGCGGATGTTGAAGTGAGCCGCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCA GGCGGATGTTGAAGTGAGCCGCATGCCCAGCTCATTTTTGTATTTTTAGTAGAGACGGGGTTTCA T G KLHDC4 Ensembl:ENSG00000104731 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1331123623 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8657,RMVar_hsa_circ_300861,RMVar_hsa_circ_112074,RMVar_hsa_circ_15052,RMVar_hsa_circ_92030,RMVar_hsa_circ_11021,RMVar_hsa_circ_39413,RMVar_hsa_circ_180432,RMVar_hsa_circ_180433,RMVar_hsa_circ_26160,RMVar_hsa_circ_319135,RMVar_hsa_circ_281186,RMVar_hsa_circ_293219,RMVar_hsa_circ_353127,RMVar_hsa_circ_110926,RMVar_hsa_circ_180435,RMVar_hsa_circ_180436,RMVar_hsa_circ_180434 22822 RMVar_ID_22822 Human_SNP_ID_613389474 A-to-I Human chr16 - 87731202 87731202 87731202 AAAATCAGCCAGGTGTGGTGGTGCACGCTTGTAATTCCAGCTACTCAGGAGGCTGAGGCAGGAGA AAAATCAGCCAGGTGTGGTGGTGCACGCTTGTCATTCCAGCTACTCAGGAGGCTGAGGCAGGAGA T G KLHDC4 Ensembl:ENSG00000104731 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1413885837 Functional Loss SNV dbSNP153 33..33 33 - - - 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 22823 RMVar_ID_22823 Human_SNP_ID_613389538 A-to-I Human chr16 - 87731361 87731361 87731361 TTACTATTAAGATAGAATTCTGGGCCGGGCACAGTGGCTCATGCCTGTAATCTCAGCACTTTGGG TTACTATTAAGATAGAATTCTGGGCCGGGCACTGTGGCTCATGCCTGTAATCTCAGCACTTTGGG T A KLHDC4 Ensembl:ENSG00000104731 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1302077958 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12838702 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 22824 RMVar_ID_22824 Human_SNP_ID_613389933 A-to-I Human chr16 - 87732156 87732156 87732156 TGGAGGCGGAGGTTGCAGGGAGCCGAGATTGCACCACTGCACTCCGGCCTGGGCAAGAATGAAAC TGGAGGCGGAGGTTGCAGGGAGCCGAGATTGCGCCACTGCACTCCGGCCTGGGCAAGAATGAAAC T C KLHDC4 Ensembl:ENSG00000104731 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1180348253 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25235518 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 22825 RMVar_ID_22825 Human_SNP_ID_613390760 A-to-I Human chr16 - 87734257 87734257 87734257 TCACTGCAGCTCCCACCTCCTGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGCA TCACTGCAGCTCCCACCTCCTGGGTTCAAGCATTTCTCCTGCCTCAGCCTCCTGAGTAGCTGGCA T A KLHDC4 Ensembl:ENSG00000104731 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs529428680 Functional Loss SNV dbSNP153 33..33 33 - - - 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 22826 RMVar_ID_22826 Human_SNP_ID_613390761 A-to-I Human chr16 - 87734257 87734257 87734257 TCACTGCAGCTCCCACCTCCTGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGCA TCACTGCAGCTCCCACCTCCTGGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCTGAGTAGCTGGCA T C KLHDC4 Ensembl:ENSG00000104731 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs529428680 Functional Loss SNV dbSNP153 33..33 33 - - - 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 22827 RMVar_ID_22827 Human_SNP_ID_613392228 A-to-I Human chr16 - 87737466 87737466 87737466 CTCTTGCCTCAGCTTTCCAAGTAGCTGGGATTACAGGTGCGCACCACCACGCTCGGCTAATTTTT CTCTTGCCTCAGCTTTCCAAGTAGCTGGGATTGCAGGTGCGCACCACCACGCTCGGCTAATTTTT T C KLHDC4 Ensembl:ENSG00000104731 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1421697690 Functional Loss SNV dbSNP153 33..33 33 - - - 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 22828 RMVar_ID_22828 Human_SNP_ID_613392339 A-to-I Human chr16 - 87737716 87737716 87737716 AGGCATGATGGTGGGCACCTGTAATTGCAGCTACTCGGGAGTCTTAGGTGGAATAATTGCTTGAA AGGCATGATGGTGGGCACCTGTAATTGCAGCTGCTCGGGAGTCTTAGGTGGAATAATTGCTTGAA T C KLHDC4 Ensembl:ENSG00000104731 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027591791 Functional Loss SNV dbSNP153 33..33 33 - - - 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 22829 RMVar_ID_22829 Human_SNP_ID_613395813 A-to-I Human chr16 - 87746154 87746154 87746154 GTGGTCTTCCTGCCTCAGCCCCCCTAGTAGCCAGGATTACAGGCGTGCACCACCGTGCCGGGCTA GTGGTCTTCCTGCCTCAGCCCCCCTAGTAGCCTGGATTACAGGCGTGCACCACCGTGCCGGGCTA T A KLHDC4,AC010536.2 Ensembl:ENSG00000104731,Ensembl:ENSG00000260671 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1226348604 Functional Loss SNV dbSNP153 33..33 33 - - - 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 22830 RMVar_ID_22830 Human_SNP_ID_613395814 A-to-I Human chr16 - 87746154 87746154 87746154 GTGGTCTTCCTGCCTCAGCCCCCCTAGTAGCCAGGATTACAGGCGTGCACCACCGTGCCGGGCTA GTGGTCTTCCTGCCTCAGCCCCCCTAGTAGCCGGGATTACAGGCGTGCACCACCGTGCCGGGCTA T C KLHDC4,AC010536.2 Ensembl:ENSG00000104731,Ensembl:ENSG00000260671 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1226348604 Functional Loss SNV dbSNP153 33..33 33 - - - 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 22831 RMVar_ID_22831 Human_SNP_ID_613397208 A-to-I Human chr16 - 87749321 87749321 87749321 TCTATTTCTTGATCTCGTGATCTGTCCACCTCAGCCTCCCGAAGTGCTGGGATTACAGGTGTGAG TCTATTTCTTGATCTCGTGATCTGTCCACCTCTGCCTCCCGAAGTGCTGGGATTACAGGTGTGAG T A KLHDC4 Ensembl:ENSG00000104731 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1408080079 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8657,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_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,RMVar_hsa_circ_321886,RMVar_hsa_circ_375196,RMVar_hsa_circ_292073,RMVar_hsa_circ_180439,RMVar_hsa_circ_180441,RMVar_hsa_circ_180442,RMVar_hsa_circ_180440 22832 RMVar_ID_22832 Human_SNP_ID_613397209 A-to-I Human chr16 - 87749321 87749321 87749321 TCTATTTCTTGATCTCGTGATCTGTCCACCTCAGCCTCCCGAAGTGCTGGGATTACAGGTGTGAG TCTATTTCTTGATCTCGTGATCTGTCCACCTCGGCCTCCCGAAGTGCTGGGATTACAGGTGTGAG T C KLHDC4 Ensembl:ENSG00000104731 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1408080079 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8657,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_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,RMVar_hsa_circ_321886,RMVar_hsa_circ_375196,RMVar_hsa_circ_292073,RMVar_hsa_circ_180439,RMVar_hsa_circ_180441,RMVar_hsa_circ_180442,RMVar_hsa_circ_180440 22833 RMVar_ID_22833 Human_SNP_ID_613397402 A-to-I Human chr16 - 87749708 87749708 87749708 ATGATGTCACATGCCTGTCGTCCAAGCTACTCAGGAGGCTGAAGTGGGAGGGTCACTTGAAACCA ATGATGTCACATGCCTGTCGTCCAAGCTACTCTGGAGGCTGAAGTGGGAGGGTCACTTGAAACCA T A KLHDC4 Ensembl:ENSG00000104731 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs929099600 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8657,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_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,RMVar_hsa_circ_321886,RMVar_hsa_circ_375196,RMVar_hsa_circ_292073,RMVar_hsa_circ_180439,RMVar_hsa_circ_180441,RMVar_hsa_circ_180442,RMVar_hsa_circ_180440 22834 RMVar_ID_22834 Human_SNP_ID_613397403 A-to-I Human chr16 - 87749708 87749708 87749708 ATGATGTCACATGCCTGTCGTCCAAGCTACTCAGGAGGCTGAAGTGGGAGGGTCACTTGAAACCA ATGATGTCACATGCCTGTCGTCCAAGCTACTCGGGAGGCTGAAGTGGGAGGGTCACTTGAAACCA T C KLHDC4 Ensembl:ENSG00000104731 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs929099600 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8657,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_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,RMVar_hsa_circ_321886,RMVar_hsa_circ_375196,RMVar_hsa_circ_292073,RMVar_hsa_circ_180439,RMVar_hsa_circ_180441,RMVar_hsa_circ_180442,RMVar_hsa_circ_180440 22835 RMVar_ID_22835 Human_SNP_ID_613397405 A-to-I Human chr16 - 87749712 87749712 87749712 GGGCATGATGTCACATGCCTGTCGTCCAAGCTACTCAGGAGGCTGAAGTGGGAGGGTCACTTGAA GGGCATGATGTCACATGCCTGTCGTCCAAGCTGCTCAGGAGGCTGAAGTGGGAGGGTCACTTGAA T C KLHDC4 Ensembl:ENSG00000104731 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1446540612 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8657,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_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,RMVar_hsa_circ_321886,RMVar_hsa_circ_375196,RMVar_hsa_circ_292073,RMVar_hsa_circ_180439,RMVar_hsa_circ_180441,RMVar_hsa_circ_180442,RMVar_hsa_circ_180440 22836 RMVar_ID_22836 Human_SNP_ID_613397407 A-to-I Human chr16 - 87749716 87749716 87749716 AGCTGGGCATGATGTCACATGCCTGTCGTCCAAGCTACTCAGGAGGCTGAAGTGGGAGGGTCACT AGCTGGGCATGATGTCACATGCCTGTCGTCCAGGCTACTCAGGAGGCTGAAGTGGGAGGGTCACT T C KLHDC4 Ensembl:ENSG00000104731 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1039745769 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8657,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_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,RMVar_hsa_circ_321886,RMVar_hsa_circ_375196,RMVar_hsa_circ_292073,RMVar_hsa_circ_180439,RMVar_hsa_circ_180441,RMVar_hsa_circ_180442,RMVar_hsa_circ_180440 22837 RMVar_ID_22837 Human_SNP_ID_613400668 A-to-I Human chr16 - 87756906 87756906 87756906 GGAGGGCTGAGGCAGGAGAATTGCTTGAACCCAGGAGTTGGAGGTTGTGGTGAGCTGAGATTGTG GGAGGGCTGAGGCAGGAGAATTGCTTGAACCCCGGAGTTGGAGGTTGTGGTGAGCTGAGATTGTG T G KLHDC4 Ensembl:ENSG00000104731 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1209656029 Functional Loss SNV dbSNP153 33..33 33 - - - 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 22838 RMVar_ID_22838 Human_SNP_ID_613400820 A-to-I Human chr16 - 87757305 87757305 87757305 CACCACCATGCCCAGCTAATTTTTCTATTTTTAGTTGAGACGGGGTTTCGCCATGTTGGCTAGGA CACCACCATGCCCAGCTAATTTTTCTATTTTTGGTTGAGACGGGGTTTCGCCATGTTGGCTAGGA T C KLHDC4 Ensembl:ENSG00000104731 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1041153258 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12839786 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 22839 RMVar_ID_22839 Human_SNP_ID_613400827 A-to-I Human chr16 - 87757320 87757320 87757320 GGGACCATAGGCACGCACCACCATGCCCAGCTAATTTTTCTATTTTTAGTTGAGACGGGGTTTCG GGGACCATAGGCACGCACCACCATGCCCAGCTGATTTTTCTATTTTTAGTTGAGACGGGGTTTCG T C KLHDC4 Ensembl:ENSG00000104731 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1004555738 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12839786 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 22840 RMVar_ID_22840 Human_SNP_ID_613400858 A-to-I Human chr16 - 87757392 87757392 87757392 ATGATCTCAGCTCACTGCAACCCCCAACTCCCAGGTTCAAGTGGTTCTCCTGCCTCAGCCTCCCG ATGATCTCAGCTCACTGCAACCCCCAACTCCCGGGTTCAAGTGGTTCTCCTGCCTCAGCCTCCCG T C KLHDC4 Ensembl:ENSG00000104731 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1353731602 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1748610 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 22841 RMVar_ID_22841 Human_SNP_ID_613400860 A-to-I Human chr16 - 87757399 87757397 87757399 CAATGGCATGATCTCAGCTCACTGCAACCCCCAACTCCCAGGTTCAAGTGGTTCTCCTGCCTCAG CAATGGCATGATCTCAGCTCACTGCAACCCCC__CTCCCAGGTTCAAGTGGTTCTCCTGCCTCAG GTT G KLHDC4 Ensembl:ENSG00000104731 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1219490119 Functional Loss DEL dbSNP153 33..34 33 - - - Human_Splice_Rec_1748610 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 22842 RMVar_ID_22842 Human_SNP_ID_613400863 A-to-I Human chr16 - 87757399 87757399 87757399 CAATGGCATGATCTCAGCTCACTGCAACCCCCAACTCCCAGGTTCAAGTGGTTCTCCTGCCTCAG CAATGGCATGATCTCAGCTCACTGCAACCCCCTACTCCCAGGTTCAAGTGGTTCTCCTGCCTCAG T A KLHDC4 Ensembl:ENSG00000104731 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1157810133 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1748610 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 22843 RMVar_ID_22843 Human_SNP_ID_613407050 A-to-I Human chr16 - 87771877 87771877 87771877 TTTGTGTTTGTAGTAGAGACGGGTTTCACCATATTGGCAAGGCTTGTCTTGAACTCCTGACCTCA TTTGTGTTTGTAGTAGAGACGGGTTTCACCATGTTGGCAAGGCTTGTCTTGAACTCCTGACCTCA T C LOC102724467 RNACentral:URS000075C3E1 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1267247723 Functional Loss SNV dbSNP153 33..33 33 - - - 22844 RMVar_ID_22844 Human_SNP_ID_613415973 A-to-I Human chr16 - 87796791 87796791 87796791 TGGGTGGCGGGTGCCTGCAAACCCAGCTACTTAGGAGGCTGAGGCAGGAGAATCGCTTGAACCTG TGGGTGGCGGGTGCCTGCAAACCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAACCTG T C AC126696.1 Ensembl:ENSG00000260177 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1193932001 Functional Loss SNV dbSNP153 33..33 33 - - - 22845 RMVar_ID_22845 Human_SNP_ID_613440752 A-to-I Human chr16 - 87866738 87866738 87866738 AAACCAGCCAGGCACTGTGGCTCACACCTGTAATCCCAGCACTTGGGAGGCCGAGGCAGGCGGAT AAACCAGCCAGGCACTGTGGCTCACACCTGTAGTCCCAGCACTTGGGAGGCCGAGGCAGGCGGAT T C SLC7A5 Ensembl:ENSG00000103257 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs750085460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12841186 RMVar_hsa_circ_110242,RMVar_hsa_circ_180446 22846 RMVar_ID_22846 Human_SNP_ID_613441258 A-to-I Human chr16 - 87868080 87868080 87868080 ACTGAGTCCCGCTCAGTCGCCCAGGCTGGAGTACAGTGGCACGATCTCGGCTCACCGCAAGCCCG ACTGAGTCCCGCTCAGTCGCCCAGGCTGGAGTGCAGTGGCACGATCTCGGCTCACCGCAAGCCCG T C SLC7A5 Ensembl:ENSG00000103257 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893149478 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2492963,Human_RBP_ID_12841236 RMVar_hsa_circ_110242,RMVar_hsa_circ_180446 22847 RMVar_ID_22847 Human_SNP_ID_613471473 A-to-I Human chr16 + 87948907 87948907 87948907 TCAAGCGAGAAGATCACTTAAGCCCGAGAGGTAGAGGCTGCAGTGAGCTCTGATTGTACCATCGC TCAAGCGAGAAGATCACTTAAGCCCGAGAGGTGGAGGCTGCAGTGAGCTCTGATTGTACCATCGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1206517484 Functional Loss SNV dbSNP153 33..33 33 - - - 22848 RMVar_ID_22848 Human_SNP_ID_613478373 A-to-I Human chr16 + 87968226 87968226 87968226 ATTTAGTTGGCTGGGTGCAGTGGCTCACCCCTATAATCCCAGCACTTTGGGAGACCGAGGTGGGT ATTTAGTTGGCTGGGTGCAGTGGCTCACCCCTGTAATCCCAGCACTTTGGGAGACCGAGGTGGGT A G BANP Ensembl:ENSG00000172530 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1385819351 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85665,RMVar_hsa_circ_27539,RMVar_hsa_circ_180460 22849 RMVar_ID_22849 Human_SNP_ID_613479073 A-to-I Human chr16 + 87970134 87970134 87970134 TTTGCCACATTGGCCAGGCTGACAGGTGATCCACCCGCCTTGGCCTTCCAAAGTGCTGGGATGAC TTTGCCACATTGGCCAGGCTGACAGGTGATCCCCCCGCCTTGGCCTTCCAAAGTGCTGGGATGAC A C BANP Ensembl:ENSG00000172530 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350640789 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1748951 RMVar_hsa_circ_180461,RMVar_hsa_circ_85665,RMVar_hsa_circ_27539,RMVar_hsa_circ_180460,RMVar_hsa_circ_89750 22850 RMVar_ID_22850 Human_SNP_ID_613514328 A-to-I Human chr16 + 88075960 88075960 88075960 TAGAGACGAGGTTTCACCATTTTGGCCAGCCTAGGCTTGAACTCCTGACCTCAAGTGATTCACCT TAGAGACGAGGTTTCACCATTTTGGCCAGCCTGGGCTTGAACTCCTGACCTCAAGTGATTCACCT A G BANP Ensembl:ENSG00000172530 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs908480720 Functional Loss SNV dbSNP153 33..33 33 - - - 22851 RMVar_ID_22851 Human_SNP_ID_613682652 A-to-I Human chr16 - 88567063 88567063 88567063 GCCTCAAGCGATCCTCCCACCTTGGCCTTCCAAAGTGCTGGGATTACAGGTGTGAGCCACTGCAT GCCTCAAGCGATCCTCCCACCTTGGCCTTCCATAGTGCTGGGATTACAGGTGTGAGCCACTGCAT T A ZC3H18-AS1,lnc-CYBA-4 RNACentral:URS0000D577BC,RNACentral:URS0000D57635 lincRNA,lincRNA exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1410793726 Functional Loss SNV dbSNP153 33..33 33 - - - 22852 RMVar_ID_22852 Human_SNP_ID_613703378 A-to-I Human chr16 + 88626084 88626084 88626084 AGCTCAGGCATTCCACCCACCTTGGCCTCCCAAAGTGCTGGGATTACATGCGTGAGCCGCCGCAC AGCTCAGGCATTCCACCCACCTTGGCCTCCCAGAGTGCTGGGATTACATGCGTGAGCCGCCGCAC A G ZC3H18 Ensembl:ENSG00000158545 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1402977465 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122783,RMVar_hsa_circ_180492,RMVar_hsa_circ_114258,RMVar_hsa_circ_180493,RMVar_hsa_circ_45728,RMVar_hsa_circ_351933 22853 RMVar_ID_22853 Human_SNP_ID_613703455 A-to-I Human chr16 + 88626294 88626294 88626294 TTTTAATTAGCTGGGTATAGTGGTGTGTGCCTATGATCCCAGCTACTTGGGAGGTCAAGGTTGAA TTTTAATTAGCTGGGTATAGTGGTGTGTGCCTGTGATCCCAGCTACTTGGGAGGTCAAGGTTGAA A G ZC3H18 Ensembl:ENSG00000158545 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs554312512 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17564444 RMVar_hsa_circ_122783,RMVar_hsa_circ_180492,RMVar_hsa_circ_114258,RMVar_hsa_circ_180493,RMVar_hsa_circ_45728,RMVar_hsa_circ_351933 22854 RMVar_ID_22854 Human_SNP_ID_613719304 A-to-I Human chr16 + 88666002 88666002 88666002 ATAGCTCACTGCAACTTCTGCCTCCTGGTTTCAAGTGATTCTCATGCCTCAGCCTCCCAAGTAGC ATAGCTCACTGCAACTTCTGCCTCCTGGTTTCCAGTGATTCTCATGCCTCAGCCTCCCAAGTAGC A C SNAI3-AS1 Ensembl:ENSG00000260630 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs760558133 Functional Loss SNV dbSNP153 33..33 33 - - - 22855 RMVar_ID_22855 Human_SNP_ID_613721048 A-to-I Human chr16 + 88670907 88670907 88670907 CCCTGATTGCACCACTGCACGGCAGCCCGAGCAACAGAGCCTGATCCTGTCTCAAGAAGAAGAAG CCCTGATTGCACCACTGCACGGCAGCCCGAGCCACAGAGCCTGATCCTGTCTCAAGAAGAAGAAG A C SNAI3-AS1 Ensembl:ENSG00000260630 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1406468515 Functional Loss SNV dbSNP153 33..33 33 - - - 22856 RMVar_ID_22856 Human_SNP_ID_613723928 A-to-I Human chr16 + 88679500 88679500 88679500 TATGAACTAGCAGGCCGGGCGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGC TATGAACTAGCAGGCCGGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGC A G SNAI3-AS1 Ensembl:ENSG00000260630 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs918480188 Functional Loss SNV dbSNP153 33..33 33 - - - 22857 RMVar_ID_22857 Human_SNP_ID_613724104 A-to-I Human chr16 + 88679824 88679824 88679824 TGAACTAGCTGGGCACAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGAGAAA TGAACTAGCTGGGCACAGTGGCTCATGCCTGTGATCCCAGCACTTTGGGAGGCCAAGGTGAGAAA A G SNAI3-AS1 Ensembl:ENSG00000260630 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1475191804 Functional Loss SNV dbSNP153 33..33 33 - - - 22858 RMVar_ID_22858 Human_SNP_ID_613724418 A-to-I Human chr16 + 88680857 88680857 88680857 GCTTGAAGTGATCCTCCCACCTCAATCTCCCAAAGTGCTGGGATTACAGGCGTGGCTCCTGCACT GCTTGAAGTGATCCTCCCACCTCAATCTCCCAGAGTGCTGGGATTACAGGCGTGGCTCCTGCACT A G SNAI3-AS1 Ensembl:ENSG00000260630 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs907222281 Functional Loss SNV dbSNP153 33..33 33 - - - 22859 RMVar_ID_22859 Human_SNP_ID_613741188 A-to-I Human chr16 - 88717873 88717873 88717873 CAAACTCCTGACCTCAAAGTGCTGGGATGACAAGTGTGAGCCGCCACACCCAGCAGTTGGGTTGT CAAACTCCTGACCTCAAAGTGCTGGGATGACAGGTGTGAGCCGCCACACCCAGCAGTTGGGTTGT T C PIEZO1 Ensembl:ENSG00000103335 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1410764154 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12881031,Human_RBP_ID_17564448 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 22860 RMVar_ID_22860 Human_SNP_ID_613741251 A-to-I Human chr16 - 88718007 88718007 88718007 ATGACCTTCACTCACTGTAGCCTCTGCCTCCCAGGTTCAAGCGATTCTCCCACCTCAGCCTCCCG ATGACCTTCACTCACTGTAGCCTCTGCCTCCCGGGTTCAAGCGATTCTCCCACCTCAGCCTCCCG T C PIEZO1 Ensembl:ENSG00000103335 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,31158229,32596459,32596459 RNA-Seq:(High) rs1309504146 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8441865,Human_RBP_ID_25236028 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 22861 RMVar_ID_22861 Human_SNP_ID_613741669 A-to-I Human chr16 - 88718852 88718852 88718852 AAAATAAACGTTAGCTGGGTGTGATGGTGCACACTTGTGCTCCCAGCTACTCTGGAGGCTGAGGT AAAATAAACGTTAGCTGGGTGTGATGGTGCACCCTTGTGCTCCCAGCTACTCTGGAGGCTGAGGT T G PIEZO1 Ensembl:ENSG00000103335 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1418506520 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2489531,Human_RBP_ID_12844574,Human_RBP_ID_17564453 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 22862 RMVar_ID_22862 Human_SNP_ID_613741734 A-to-I Human chr16 - 88718996 88718996 88718996 ATGTAAAAATAAAACAATTAGCTGGCAATGGCAGCTCATGCCTATGGTCCCAGCACTTTGGGAGG ATGTAAAAATAAAACAATTAGCTGGCAATGGCTGCTCATGCCTATGGTCCCAGCACTTTGGGAGG T A PIEZO1 Ensembl:ENSG00000103335 Protein coding intron GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,29796672,31158229,32596459 RNA-Seq:(High) rs942620798 Functional Loss SNV dbSNP153 33..33 33 - - - 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 22863 RMVar_ID_22863 Human_SNP_ID_613758752 A-to-I Human chr16 - 88749856 88749856 88749856 GCCCGGCTAATTTTTGTATTTTCGGTGGAGACAGGGTTTCACCACGTTGGCCAGGCTGGTCTTGA GCCCGGCTAATTTTTGTATTTTCGGTGGAGACGGGGTTTCACCACGTTGGCCAGGCTGGTCTTGA T C PIEZO1 Ensembl:ENSG00000103335 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560346071 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93984,RMVar_hsa_circ_90544,RMVar_hsa_circ_180534,RMVar_hsa_circ_180538,RMVar_hsa_circ_75665,RMVar_hsa_circ_180553 22864 RMVar_ID_22864 Human_SNP_ID_613768787 A-to-I Human chr16 - 88777168 88777168 88777168 AGGAGTTCAAGACCAGCCTGGCCAACATGGCAAAACCCTGTCCCTACTGAAAATACAAAAATTAG AGGAGTTCAAGACCAGCCTGGCCAACATGGCAGAACCCTGTCCCTACTGAAAATACAAAAATTAG T C PIEZO1 Ensembl:ENSG00000103335 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs566273153 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93984,RMVar_hsa_circ_90544,RMVar_hsa_circ_180534,RMVar_hsa_circ_180538,RMVar_hsa_circ_75665,RMVar_hsa_circ_180553 22865 RMVar_ID_22865 Human_SNP_ID_613796190 A-to-I Human chr16 - 88846683 88846683 88846683 CAAAAACTAGCTGAGCATGATGGAGGGCGCCTATAATCCCAGCTACTTGGGAGGCTGAGGCAGGA CAAAAACTAGCTGAGCATGATGGAGGGCGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGA T C GALNS Ensembl:ENSG00000141012 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1336450322 Functional Loss SNV dbSNP153 33..33 33 - - - 22866 RMVar_ID_22866 Human_SNP_ID_613796196 A-to-I Human chr16 - 88846707 88846706 88846707 GAAACCCCGTCTCTACTAAAAATACAAAAACTAGCTGAGCATGATGGAGGGCGCCTATAATCCCA GAAACCCCGTCTCTACTAAAAATACAAAAACT_GCTGAGCATGATGGAGGGCGCCTATAATCCCA CT C GALNS Ensembl:ENSG00000141012 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1427422686 Functional Loss DEL dbSNP153 33..33 33 - - - 22867 RMVar_ID_22867 Human_SNP_ID_613908191 A-to-I Human chr16 + 89152421 89152421 89152421 CCTGACGTCAGGAGTTGGAGACCATCCTGGCCAACATGGTGAAACCCCGTCTCTATTAAAAATAC CCTGACGTCAGGAGTTGGAGACCATCCTGGCCCACATGGTGAAACCCCGTCTCTATTAAAAATAC A C ACSF3 Ensembl:ENSG00000176715 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1237218138 Functional Loss SNV dbSNP153 33..33 33 - - - 22868 RMVar_ID_22868 Human_SNP_ID_613908199 A-to-I Human chr16 + 89152443 89152443 89152443 CATCCTGGCCAACATGGTGAAACCCCGTCTCTATTAAAAATACAAAAATTAGCCAGGCATGGTGG CATCCTGGCCAACATGGTGAAACCCCGTCTCTGTTAAAAATACAAAAATTAGCCAGGCATGGTGG A G ACSF3 Ensembl:ENSG00000176715 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1343584881 Functional Loss SNV dbSNP153 33..33 33 - - - 22869 RMVar_ID_22869 Human_SNP_ID_613908218 A-to-I Human chr16 + 89152487 89152487 89152487 AAAATTAGCCAGGCATGGTGGTATGCGCCTGTAGTCCCAGCTAGTTAGGAGGCTGAGGCAGGAGA AAAATTAGCCAGGCATGGTGGTATGCGCCTGTCGTCCCAGCTAGTTAGGAGGCTGAGGCAGGAGA A C ACSF3 Ensembl:ENSG00000176715 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1045155898 Functional Loss SNV dbSNP153 33..33 33 - - - 22870 RMVar_ID_22870 Human_SNP_ID_613919057 A-to-I Human chr16 + 89181190 89181190 89181190 GGGGTTTCACCATGTTGGCCTCCCAAAGTGCTAGGATTACAGGCGTGAGCCACCACACCTGGCCC GGGGTTTCACCATGTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCACACCTGGCCC A G CDH15 Ensembl:ENSG00000129910 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs181834189 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_180591,RMVar_hsa_circ_95824 22871 RMVar_ID_22871 Human_SNP_ID_613957703 A-to-I Human chr16 - 89273585 89273585 89273585 TCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATCACAGGCATGCGCTACCATGCCCG TCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTGGCTGGGATCACAGGCATGCGCTACCATGCCCG T C ANKRD11 Ensembl:ENSG00000167522 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1433704767 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119796,RMVar_hsa_circ_321069,RMVar_hsa_circ_180603,RMVar_hsa_circ_116892,RMVar_hsa_circ_180604,RMVar_hsa_circ_180602 22872 RMVar_ID_22872 Human_SNP_ID_613964180 A-to-I Human chr16 - 89286891 89286891 89286891 GTAAACGTTATGACAGATTCTTTGAATGCGCTAATCTCAGACTGGACTAAAGTTGGGATTAAATT GTAAACGTTATGACAGATTCTTTGAATGCGCTTATCTCAGACTGGACTAAAGTTGGGATTAAATT T A ANKRD11 Ensembl:ENSG00000167522 Protein coding intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1362452517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_481763,Human_RBP_ID_1525156,Human_RBP_ID_1847822,Human_RBP_ID_8442280,Human_RBP_ID_12847889,Human_RBP_ID_22207514,Human_RBP_ID_23706537,Human_RBP_ID_27447371 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_180608 22873 RMVar_ID_22873 Human_SNP_ID_613996583 A-to-I Human chr16 - 89384218 89384218 89384218 CCTTGAGAAATGTTTGTTTTTGTTTGTTTTTGAGATGGAGTCTCGCTCTGTCACCCAGGCTGGAG CCTTGAGAAATGTTTGTTTTTGTTTGTTTTTGCGATGGAGTCTCGCTCTGTCACCCAGGCTGGAG T G ANKRD11 Ensembl:ENSG00000167522 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1021962226 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12850458 RMVar_hsa_circ_119796,RMVar_hsa_circ_180603,RMVar_hsa_circ_116892,RMVar_hsa_circ_180604,RMVar_hsa_circ_325779,RMVar_hsa_circ_329884 22874 RMVar_ID_22874 Human_SNP_ID_613997026 A-to-I Human chr16 - 89385165 89385165 89385165 ACAAAAAAACACCATTTCTCAAGGCCGGGTACAGTGGCTCACGCCTGTAATCCCAGCACTTTGGG ACAAAAAAACACCATTTCTCAAGGCCGGGTACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG T C ANKRD11 Ensembl:ENSG00000167522 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1399868503 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 22875 RMVar_ID_22875 Human_SNP_ID_613997757 A-to-I Human chr16 - 89387416 89387416 89387416 TGCCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGAGTGAGCCACCGCGCCCGGCCCAAGCAC TGCCCGCCTCAGCCTCCCAAAGTGCTGGGATTGCAGGAGTGAGCCACCGCGCCCGGCCCAAGCAC T C ANKRD11 Ensembl:ENSG00000167522 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913980869 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 22876 RMVar_ID_22876 Human_SNP_ID_613998416 A-to-I Human chr16 - 89389292 89389292 89389292 GGTCGGGTGTGGTGGCTCACGCCTGTAATCCCAGCACTGTAGGAAGCCAAGGTGGGAAGATTGCT GGTCGGGTGTGGTGGCTCACGCCTGTAATCCCGGCACTGTAGGAAGCCAAGGTGGGAAGATTGCT T C ANKRD11 Ensembl:ENSG00000167522 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs895649111 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 22877 RMVar_ID_22877 Human_SNP_ID_613999993 A-to-I Human chr16 - 89393615 89393615 89393615 AAACTAGGCCGGGCGCAGTGGCTTCCTCCTGTAATCCCACCACTTTGGGAGGCTGAGGCGGGCAA AAACTAGGCCGGGCGCAGTGGCTTCCTCCTGTCATCCCACCACTTTGGGAGGCTGAGGCGGGCAA T G ANKRD11 Ensembl:ENSG00000167522 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs562663622 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 22878 RMVar_ID_22878 Human_SNP_ID_614003734 A-to-I Human chr16 - 89405402 89405402 89405402 GGAGGATCGCCTGAGCCCAGGAGGTCGAGGCTACGGTGAGCTCATATCACACCACTGCACTCTAG GGAGGATCGCCTGAGCCCAGGAGGTCGAGGCTGCGGTGAGCTCATATCACACCACTGCACTCTAG T C ANKRD11 Ensembl:ENSG00000167522 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054574636 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17564859 RMVar_hsa_circ_119796,RMVar_hsa_circ_180603,RMVar_hsa_circ_116892,RMVar_hsa_circ_180604,RMVar_hsa_circ_325779,RMVar_hsa_circ_329884 22879 RMVar_ID_22879 Human_SNP_ID_614003916 A-to-I Human chr16 - 89405927 89405927 89405927 TTTTGTCTTTTTAGTAGAGACGGGGCTTTACCATGTTGGCCAGACTGCTCTCGAACTCCTGTCCT TTTTGTCTTTTTAGTAGAGACGGGGCTTTACCGTGTTGGCCAGACTGCTCTCGAACTCCTGTCCT T C ANKRD11 Ensembl:ENSG00000167522 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs894771220 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12851268 RMVar_hsa_circ_119796,RMVar_hsa_circ_180603,RMVar_hsa_circ_116892,RMVar_hsa_circ_180604,RMVar_hsa_circ_325779,RMVar_hsa_circ_329884 22880 RMVar_ID_22880 Human_SNP_ID_614007070 A-to-I Human chr16 - 89415781 89415781 89415781 TTGTTGTGCAGGGCCTGGAGTGTAGTGGTGCAATCTCGGCTCACTGCAACCTCCACCTCCCAGAT TTGTTGTGCAGGGCCTGGAGTGTAGTGGTGCAGTCTCGGCTCACTGCAACCTCCACCTCCCAGAT T C ANKRD11 Ensembl:ENSG00000167522 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1426032028 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 22881 RMVar_ID_22881 Human_SNP_ID_614024739 A-to-I Human chr16 - 89467253 89467253 89467253 TTCTGTTTTTTTTTTTTGTAGAGATGGGGTTTAGCCATGTTGCCCTGGCCCATCTCAAACTCCTG TTCTGTTTTTTTTTTTTGTAGAGATGGGGTTTGGCCATGTTGCCCTGGCCCATCTCAAACTCCTG T C ANKRD11 Ensembl:ENSG00000167522 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1368281435 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12853935,Human_RBP_ID_17563886 RMVar_hsa_circ_116892,RMVar_hsa_circ_180604 22882 RMVar_ID_22882 Human_SNP_ID_614025147 A-to-I Human chr16 - 89468644 89468644 89468644 GGAGTGCAGTGGCGCGATCTCGGCTCACTGCAACCTCTGCCTCCCAGGTTCCCAAGCAATTCTCC GGAGTGCAGTGGCGCGATCTCGGCTCACTGCAGCCTCTGCCTCCCAGGTTCCCAAGCAATTCTCC T C ANKRD11 Ensembl:ENSG00000167522 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1203770760 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12853989 RMVar_hsa_circ_116892,RMVar_hsa_circ_180604 22883 RMVar_ID_22883 Human_SNP_ID_614025167 A-to-I Human chr16 - 89468701 89468701 89468701 ACTTTTGCTTCGTCCTTCTTTTTTTTTGAGATAGCGTCTTACTCTGTTGCCCAGGCTGGAGTGCA ACTTTTGCTTCGTCCTTCTTTTTTTTTGAGATGGCGTCTTACTCTGTTGCCCAGGCTGGAGTGCA T C ANKRD11 Ensembl:ENSG00000167522 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs557941264 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12853992 RMVar_hsa_circ_116892,RMVar_hsa_circ_180604 22884 RMVar_ID_22884 Human_SNP_ID_614025402 A-to-I Human chr16 - 89469411 89469411 89469411 TGACACCATCCTGGGCAACACAGTGAAACCCTATCTTTACTGAAATGCAAAAAAATTAGCTGGAC TGACACCATCCTGGGCAACACAGTGAAACCCTGTCTTTACTGAAATGCAAAAAAATTAGCTGGAC T C ANKRD11 Ensembl:ENSG00000167522 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1465634204 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23165971 RMVar_hsa_circ_116892,RMVar_hsa_circ_180604 22885 RMVar_ID_22885 Human_SNP_ID_614033290 A-to-I Human chr16 + 89491938 89491938 89491938 ACCCGGCTAATTTTTTAAATTTTCGTAGAGATAGGCTCTCTGTGTGTTTCCCAGGCTGGTCTTGA ACCCGGCTAATTTTTTAAATTTTCGTAGAGATGGGCTCTCTGTGTGTTTCCCAGGCTGGTCTTGA A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1457793950 Functional Loss SNV dbSNP153 33..33 33 - - - 22886 RMVar_ID_22886 Human_SNP_ID_614033434 A-to-I Human chr16 - 89492409 89492409 89492409 GTATTGTAAGGGACCAAAATAAAAAAATGCCAATGCCTAGTCCCCTCTCATCTAGAATAATTCCA GTATTGTAAGGGACCAAAATAAAAAAATGCCAGTGCCTAGTCCCCTCTCATCTAGAATAATTCCA T C AC092123.1 Ensembl:ENSG00000261118 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs898983185 Functional Loss SNV dbSNP153 33..33 33 - - - 22887 RMVar_ID_22887 Human_SNP_ID_614035039 A-to-I Human chr16 + 89497156 89497156 89497156 GGAGTTCGAGACCAGCCTGGCCAACGTGGTGAAACCCTGTCTGTACTCAAAATAGAAAAATTAGC GGAGTTCGAGACCAGCCTGGCCAACGTGGTGATACCCTGTCTGTACTCAAAATAGAAAAATTAGC A T SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1275508325 Functional Loss SNV dbSNP153 33..33 33 - - - 22888 RMVar_ID_22888 Human_SNP_ID_614041274 A-to-I Human chr16 + 89513355 89513355 89513355 CCTGGCCAACATGGTGAAACCCCGTCTTTACTAAAAATAGAAAATTAGCCGGGCGTGATGGCACA CCTGGCCAACATGGTGAAACCCCGTCTTTACTGAAAATAGAAAATTAGCCGGGCGTGATGGCACA A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs540563488 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_84 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 22889 RMVar_ID_22889 Human_SNP_ID_614041776 A-to-I Human chr16 + 89514700 89514700 89514700 TTTTTTTGTTTTATTAGAGACTGGGTTTCACCATGTTAGCCAGGATGGTCTCGATCTCCTGACCT TTTTTTTGTTTTATTAGAGACTGGGTTTCACCCTGTTAGCCAGGATGGTCTCGATCTCCTGACCT A C SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs921569842 Functional Loss SNV dbSNP153 33..33 33 - - - 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 22890 RMVar_ID_22890 Human_SNP_ID_614041778 A-to-I Human chr16 + 89514705 89514705 89514705 TTGTTTTATTAGAGACTGGGTTTCACCATGTTAGCCAGGATGGTCTCGATCTCCTGACCTTGTGA TTGTTTTATTAGAGACTGGGTTTCACCATGTTTGCCAGGATGGTCTCGATCTCCTGACCTTGTGA A T SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs961328074 Functional Loss SNV dbSNP153 33..33 33 - - - 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 22891 RMVar_ID_22891 Human_SNP_ID_614041798 A-to-I Human chr16 + 89514759 89514759 89514759 TGACCTTGTGATCTGCTCACCTTGGCCTCCCAAAGTTCTAGGATTACAGGCGTGAGCCACCGCGT TGACCTTGTGATCTGCTCACCTTGGCCTCCCAGAGTTCTAGGATTACAGGCGTGAGCCACCGCGT A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1420700264 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12855465,Human_RBP_ID_22715593,Human_RBP_ID_23166020 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 22892 RMVar_ID_22892 Human_SNP_ID_614041802 A-to-I Human chr16 + 89514766 89514766 89514766 GTGATCTGCTCACCTTGGCCTCCCAAAGTTCTAGGATTACAGGCGTGAGCCACCGCGTCAGGCCC GTGATCTGCTCACCTTGGCCTCCCAAAGTTCTGGGATTACAGGCGTGAGCCACCGCGTCAGGCCC A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1264209212 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12855465,Human_RBP_ID_22715593,Human_RBP_ID_23166020 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 22893 RMVar_ID_22893 Human_SNP_ID_614041803 A-to-I Human chr16 + 89514766 89514766 89514766 GTGATCTGCTCACCTTGGCCTCCCAAAGTTCTAGGATTACAGGCGTGAGCCACCGCGTCAGGCCC GTGATCTGCTCACCTTGGCCTCCCAAAGTTCTTGGATTACAGGCGTGAGCCACCGCGTCAGGCCC A T SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1264209212 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12855465,Human_RBP_ID_22715593,Human_RBP_ID_23166020 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 22894 RMVar_ID_22894 Human_SNP_ID_614041826 A-to-I Human chr16 + 89514808 89514808 89514808 GCGTGAGCCACCGCGTCAGGCCCTCTTTTTGTATAGTAGAGATGAGGTTTTGTCTTGTTGGCCAG GCGTGAGCCACCGCGTCAGGCCCTCTTTTTGTGTAGTAGAGATGAGGTTTTGTCTTGTTGGCCAG A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs8046182 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12855466,Human_RBP_ID_23166022 GWAS_ID_2111,GWAS_ID_2112,GWAS_ID_2113 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 22895 RMVar_ID_22895 Human_SNP_ID_614041827 A-to-I Human chr16 + 89514808 89514808 89514808 GCGTGAGCCACCGCGTCAGGCCCTCTTTTTGTATAGTAGAGATGAGGTTTTGTCTTGTTGGCCAG GCGTGAGCCACCGCGTCAGGCCCTCTTTTTGTTTAGTAGAGATGAGGTTTTGTCTTGTTGGCCAG A T SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs8046182 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12855466,Human_RBP_ID_23166022 GWAS_ID_2111,GWAS_ID_2112,GWAS_ID_2113 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 22896 RMVar_ID_22896 Human_SNP_ID_614041950 A-to-I Human chr16 + 89515118 89515118 89515118 GCCACCATACCCGGCTCATTTTTTGTATTTTTAGTAGAGACTCGGTTTCACCGTGTTAGCCAGGA GCCACCATACCCGGCTCATTTTTTGTATTTTTGGTAGAGACTCGGTTTCACCGTGTTAGCCAGGA A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1307296921 Functional Loss SNV dbSNP153 33..33 33 - - - 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 22897 RMVar_ID_22897 Human_SNP_ID_614041951 A-to-I Human chr16 + 89515121 89515121 89515121 ACCATACCCGGCTCATTTTTTGTATTTTTAGTAGAGACTCGGTTTCACCGTGTTAGCCAGGATGG ACCATACCCGGCTCATTTTTTGTATTTTTAGTGGAGACTCGGTTTCACCGTGTTAGCCAGGATGG A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1171965947 Functional Loss SNV dbSNP153 33..33 33 - - - 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 22898 RMVar_ID_22898 Human_SNP_ID_614042016 A-to-I Human chr16 + 89515289 89515289 89515289 CTTTTATTTTGTATTTATTTATTTATTTTTGAAACGGAGTCTCGCTCTGTTGCCCAGACTGGAGT CTTTTATTTTGTATTTATTTATTTATTTTTGAGACGGAGTCTCGCTCTGTTGCCCAGACTGGAGT A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1312776277 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2490663,Human_RBP_ID_12855472,Human_RBP_ID_17565282,Human_RBP_ID_22474061,Human_RBP_ID_22943652,Human_RBP_ID_23166026,Human_RBP_ID_25236987 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 22899 RMVar_ID_22899 Human_SNP_ID_614042045 A-to-I Human chr16 + 89515363 89515363 89515363 CGATGTCGGCTCAGTGCAACCCCTGCCTCCTGAGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGA CGATGTCGGCTCAGTGCAACCCCTGCCTCCTGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGA A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1342014861 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12855472 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 22900 RMVar_ID_22900 Human_SNP_ID_614042046 A-to-I Human chr16 + 89515368 89515368 89515368 TCGGCTCAGTGCAACCCCTGCCTCCTGAGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGC TCGGCTCAGTGCAACCCCTGCCTCCTGAGTTCGAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGC A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs556840621 Functional Loss SNV dbSNP153 33..33 33 - - - 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 22901 RMVar_ID_22901 Human_SNP_ID_614042054 A-to-I Human chr16 + 89515386 89515386 89515386 TGCCTCCTGAGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCATGCA TGCCTCCTGAGTTCAAGCGATTCTCCTGCCTCGGCCTCCTGAGTAGCTGGGATTACAGGCATGCA A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924194171 Functional Loss SNV dbSNP153 33..33 33 - - - 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 22902 RMVar_ID_22902 Human_SNP_ID_614042073 A-to-I Human chr16 + 89515469 89515469 89515469 TTTTGTATTTTCAGTAGATACAGGGTTTTGCCATGTTGGCCAGACTGGTCTTGAACTCCTGACCT TTTTGTATTTTCAGTAGATACAGGGTTTTGCCGTGTTGGCCAGACTGGTCTTGAACTCCTGACCT A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1343217877 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12855479 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 22903 RMVar_ID_22903 Human_SNP_ID_614042086 A-to-I Human chr16 + 89515514 89515514 89515514 TGGTCTTGAACTCCTGACCTCGTGATCTCCCCACTTCGGCCTCCCAAAGTGCTGGGATTACAGGT TGGTCTTGAACTCCTGACCTCGTGATCTCCCCGCTTCGGCCTCCCAAAGTGCTGGGATTACAGGT A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1478210448 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25236990,Human_RBP_ID_27447438 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 22904 RMVar_ID_22904 Human_SNP_ID_614042271 A-to-I Human chr16 + 89515883 89515883 89515883 GCGTGCGCCACCACGCCCAGCTAATTTTTTGTATTTTTAGCAGAGACAGGGTTTCACCATGTTGG GCGTGCGCCACCACGCCCAGCTAATTTTTTGTGTTTTTAGCAGAGACAGGGTTTCACCATGTTGG A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1193282702 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12855494 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 22905 RMVar_ID_22905 Human_SNP_ID_614042277 A-to-I Human chr16 + 89515909 89515909 89515909 TTTTGTATTTTTAGCAGAGACAGGGTTTCACCATGTTGGCAAGGATGGTCTCAAACTCCCGATGT TTTTGTATTTTTAGCAGAGACAGGGTTTCACCGTGTTGGCAAGGATGGTCTCAAACTCCCGATGT A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs748300919 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5128927,Human_RBP_ID_12855495,Human_RBP_ID_22474639,Human_RBP_ID_25237002 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 22906 RMVar_ID_22906 Human_SNP_ID_614042281 A-to-I Human chr16 + 89515917 89515917 89515917 TTTTAGCAGAGACAGGGTTTCACCATGTTGGCAAGGATGGTCTCAAACTCCCGATGTCAGGCGAT TTTTAGCAGAGACAGGGTTTCACCATGTTGGCGAGGATGGTCTCAAACTCCCGATGTCAGGCGAT A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1287593356 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5128927,Human_RBP_ID_12855497,Human_RBP_ID_22474639,Human_RBP_ID_23166034 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 22907 RMVar_ID_22907 Human_SNP_ID_614042296 A-to-I Human chr16 + 89515970 89515970 89515970 ATGTCAGGCGATCTGCCCATCTTGGCCTTCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGTGC ATGTCAGGCGATCTGCCCATCTTGGCCTTCCAGAGTGCTGGGATTACAGGTGTGAGCCACCGTGC A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs529016292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12855502 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 22908 RMVar_ID_22908 Human_SNP_ID_614042313 A-to-I Human chr16 + 89516018 89516018 89516018 GGTGTGAGCCACCGTGCCCAGCCTGGAGTTTCACTCTTGTTTCCCAGGCTAGAGTGCAATGGCGT GGTGTGAGCCACCGTGCCCAGCCTGGAGTTTCGCTCTTGTTTCCCAGGCTAGAGTGCAATGGCGT A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1196189565 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12855504,Human_RBP_ID_23166036 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 22909 RMVar_ID_22909 Human_SNP_ID_614042321 A-to-I Human chr16 + 89516036 89516036 89516036 CAGCCTGGAGTTTCACTCTTGTTTCCCAGGCTAGAGTGCAATGGCGTAATTTCAGATCACTGGAA CAGCCTGGAGTTTCACTCTTGTTTCCCAGGCTGGAGTGCAATGGCGTAATTTCAGATCACTGGAA A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1344816959 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12855506,Human_RBP_ID_22474640 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 22910 RMVar_ID_22910 Human_SNP_ID_614042381 A-to-I Human chr16 + 89516202 89516202 89516202 TAGAGACCTGGTTTGGCCACGTTGGTCAGGCTAGTCTCAAACTTCTCACCTCAGGTGATCCACTC TAGAGACCTGGTTTGGCCACGTTGGTCAGGCTGGTCTCAAACTTCTCACCTCAGGTGATCCACTC A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs541195908 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5128929,Human_RBP_ID_12855515,Human_RBP_ID_17563888,Human_RBP_ID_22474064 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 22911 RMVar_ID_22911 Human_SNP_ID_614042441 A-to-I Human chr16 + 89516355 89516355 89516355 CTTGGGGCCAGGAGTTCGAGACCAGCCTGGCTAACATGGTGAAACCCCTTGTCTACTAAAAATAC CTTGGGGCCAGGAGTTCGAGACCAGCCTGGCTGACATGGTGAAACCCCTTGTCTACTAAAAATAC A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE38233;GSE100210;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,cerebellum - 24183664,29129909,30559470 RNA-Seq:(High) rs1035267438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22946497,Human_RBP_ID_25237017 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 22912 RMVar_ID_22912 Human_SNP_ID_614042443 A-to-I Human chr16 + 89516358 89516358 89516358 GGGGCCAGGAGTTCGAGACCAGCCTGGCTAACATGGTGAAACCCCTTGTCTACTAAAAATACCAA GGGGCCAGGAGTTCGAGACCAGCCTGGCTAACGTGGTGAAACCCCTTGTCTACTAAAAATACCAA A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1457688150 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22946497,Human_RBP_ID_25237017 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 22913 RMVar_ID_22913 Human_SNP_ID_614042477 A-to-I Human chr16 + 89516409 89516409 89516409 ACTAAAAATACCAAAAAAAAAAAAAATTAGCCAGGTGTGGTGTACGTGCTTGTAATCCCAGCTAC ACTAAAAATACCAAAAAAAAAAAAAATTAGCCGGGTGTGGTGTACGTGCTTGTAATCCCAGCTAC A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1434306741 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12855524 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 22914 RMVar_ID_22914 Human_SNP_ID_614042509 A-to-I Human chr16 + 89516483 89516483 89516483 TGAGGCGTGAGCATCGTTTGAACCTGGTAGGCAGAGGTTGCAGGGAGCTGAGATTGTGCCATTGC TGAGGCGTGAGCATCGTTTGAACCTGGTAGGCGGAGGTTGCAGGGAGCTGAGATTGTGCCATTGC A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1044830209 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9840251,Human_RBP_ID_12855528,Human_RBP_ID_17563889,Human_RBP_ID_22474065,Human_RBP_ID_22715594,Human_RBP_ID_25237020 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 22915 RMVar_ID_22915 Human_SNP_ID_614042557 A-to-I Human chr16 + 89516643 89516643 89516643 AGCACTTTGGGAGGCCAAGGCGAGCAGATCACAAGGTCAGGAGATCGAGACCATTTTAGCTAACA AGCACTTTGGGAGGCCAAGGCGAGCAGATCACGAGGTCAGGAGATCGAGACCATTTTAGCTAACA A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1024168049 Functional Loss SNV dbSNP153 33..33 33 - - - 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 22916 RMVar_ID_22916 Human_SNP_ID_614042640 A-to-I Human chr16 + 89516852 89516852 89516852 GCGCCACTGCACTCCAGCCTGGGCGACACAGCAAGACTCTGTCTCAAAAAAAAAAATTAAGAAAG GCGCCACTGCACTCCAGCCTGGGCGACACAGCCAGACTCTGTCTCAAAAAAAAAAATTAAGAAAG A C SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1234111000 Functional Loss SNV dbSNP153 33..33 33 - - - 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 22917 RMVar_ID_22917 Human_SNP_ID_614042969 A-to-I Human chr16 + 89517694 89517694 89517694 GAAGTTGGAGTGCAATGCCACGATCTCGGCTCATTGCAAACTCCACCTCGTGGGTTCAAGCAGTT GAAGTTGGAGTGCAATGCCACGATCTCGGCTCGTTGCAAACTCCACCTCGTGGGTTCAAGCAGTT A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs143343236 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12855574 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 22918 RMVar_ID_22918 Human_SNP_ID_614042970 A-to-I Human chr16 + 89517694 89517694 89517694 GAAGTTGGAGTGCAATGCCACGATCTCGGCTCATTGCAAACTCCACCTCGTGGGTTCAAGCAGTT GAAGTTGGAGTGCAATGCCACGATCTCGGCTCTTTGCAAACTCCACCTCGTGGGTTCAAGCAGTT A T SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs143343236 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12855574 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 22919 RMVar_ID_22919 Human_SNP_ID_614042972 A-to-I Human chr16 + 89517699 89517699 89517699 TGGAGTGCAATGCCACGATCTCGGCTCATTGCAAACTCCACCTCGTGGGTTCAAGCAGTTCTCCT TGGAGTGCAATGCCACGATCTCGGCTCATTGCGAACTCCACCTCGTGGGTTCAAGCAGTTCTCCT A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1319119012 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12855574,Human_RBP_ID_26952663 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 22920 RMVar_ID_22920 Human_SNP_ID_614043003 A-to-I Human chr16 + 89517804 89517804 89517804 ACCATGCCCGGCTAATTTTTTGTGTTTTTAGTAGAGACGGAGTTTCACCATGTGAGCTAGGATGA ACCATGCCCGGCTAATTTTTTGTGTTTTTAGTGGAGACGGAGTTTCACCATGTGAGCTAGGATGA A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs921208710 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12855579,Human_RBP_ID_22946503 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 22921 RMVar_ID_22921 Human_SNP_ID_614043009 A-to-I Human chr16 + 89517821 89517821 89517821 TTTTGTGTTTTTAGTAGAGACGGAGTTTCACCATGTGAGCTAGGATGATCTCGATCTCCTGACGT TTTTGTGTTTTTAGTAGAGACGGAGTTTCACCCTGTGAGCTAGGATGATCTCGATCTCCTGACGT A C SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1053513684 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12855581,Human_RBP_ID_26952667 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 22922 RMVar_ID_22922 Human_SNP_ID_614043032 A-to-I Human chr16 + 89517880 89517880 89517880 TGACGTTGTGGTCTGCCCACCTCGGCCTCCCAAAGTGCTGGGATTATAGGCGTGAGCCACCACGC TGACGTTGTGGTCTGCCCACCTCGGCCTCCCAGAGTGCTGGGATTATAGGCGTGAGCCACCACGC A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1225894854 Functional Loss SNV dbSNP153 33..33 33 - - - 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 22923 RMVar_ID_22923 Human_SNP_ID_614043507 A-to-I Human chr16 + 89519219 89519219 89519219 GTTGGTCAGGCTGGTCTCGAACTCCTGACCTCATCATCTGCCTGCCTCGGTCCCCACAAAGTGCT GTTGGTCAGGCTGGTCTCGAACTCCTGACCTCCTCATCTGCCTGCCTCGGTCCCCACAAAGTGCT A C SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11076606 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25247311 Clinvar_Rec_85,Clinvar_Rec_86 GWAS_ID_2114,GWAS_ID_2115,GWAS_ID_2116,GWAS_ID_2117,GWAS_ID_2118,GWAS_ID_2119,GWAS_ID_2120,GWAS_ID_2121,GWAS_ID_2122,GWAS_ID_2123,GWAS_ID_2124,GWAS_ID_2125,GWAS_ID_2126,GWAS_ID_2127,GWAS_ID_2128,GWAS_ID_2129,GWAS_ID_2130,GWAS_ID_2131,GWAS_ID_2132,GWAS_ID_2133,GWAS_ID_2134,GWAS_ID_2135,GWAS_ID_2136,GWAS_ID_2137,GWAS_ID_2138,GWAS_ID_2139,GWAS_ID_2140,GWAS_ID_2141,GWAS_ID_2142,GWAS_ID_2143,GWAS_ID_2144,GWAS_ID_2145,GWAS_ID_2146,GWAS_ID_2147,GWAS_ID_2148,GWAS_ID_2149,GWAS_ID_2150,GWAS_ID_2151,GWAS_ID_2152,GWAS_ID_2153,GWAS_ID_2154,GWAS_ID_2155,GWAS_ID_2156,GWAS_ID_2157,GWAS_ID_2158,GWAS_ID_2159,GWAS_ID_2160,GWAS_ID_2161,GWAS_ID_2162,GWAS_ID_2163,GWAS_ID_2164,GWAS_ID_2165,GWAS_ID_2166,GWAS_ID_2167,GWAS_ID_2168,GWAS_ID_2169,GWAS_ID_2170,GWAS_ID_2171,GWAS_ID_2172,GWAS_ID_2173 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 22924 RMVar_ID_22924 Human_SNP_ID_614043508 A-to-I Human chr16 + 89519219 89519219 89519219 GTTGGTCAGGCTGGTCTCGAACTCCTGACCTCATCATCTGCCTGCCTCGGTCCCCACAAAGTGCT GTTGGTCAGGCTGGTCTCGAACTCCTGACCTCGTCATCTGCCTGCCTCGGTCCCCACAAAGTGCT A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11076606 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25247311 Clinvar_Rec_85,Clinvar_Rec_86 GWAS_ID_2114,GWAS_ID_2115,GWAS_ID_2116,GWAS_ID_2117,GWAS_ID_2118,GWAS_ID_2119,GWAS_ID_2120,GWAS_ID_2121,GWAS_ID_2122,GWAS_ID_2123,GWAS_ID_2124,GWAS_ID_2125,GWAS_ID_2126,GWAS_ID_2127,GWAS_ID_2128,GWAS_ID_2129,GWAS_ID_2130,GWAS_ID_2131,GWAS_ID_2132,GWAS_ID_2133,GWAS_ID_2134,GWAS_ID_2135,GWAS_ID_2136,GWAS_ID_2137,GWAS_ID_2138,GWAS_ID_2139,GWAS_ID_2140,GWAS_ID_2141,GWAS_ID_2142,GWAS_ID_2143,GWAS_ID_2144,GWAS_ID_2145,GWAS_ID_2146,GWAS_ID_2147,GWAS_ID_2148,GWAS_ID_2149,GWAS_ID_2150,GWAS_ID_2151,GWAS_ID_2152,GWAS_ID_2153,GWAS_ID_2154,GWAS_ID_2155,GWAS_ID_2156,GWAS_ID_2157,GWAS_ID_2158,GWAS_ID_2159,GWAS_ID_2160,GWAS_ID_2161,GWAS_ID_2162,GWAS_ID_2163,GWAS_ID_2164,GWAS_ID_2165,GWAS_ID_2166,GWAS_ID_2167,GWAS_ID_2168,GWAS_ID_2169,GWAS_ID_2170,GWAS_ID_2171,GWAS_ID_2172,GWAS_ID_2173 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 22925 RMVar_ID_22925 Human_SNP_ID_614043577 A-to-I Human chr16 + 89519405 89519397 89519406 GCTAACATTTTTTTTTTCTTTTTTTGAGACGGAATTTCGCTCTTGTTGCCCAGCCTGGAGTGCAG GCTAACATTTTTTTTTTCTTTTTTT_________TTTCGCTCTTGTTGCCCAGCCTGGAGTGCAG TGAGACGGAA T SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1429864764 Functional Loss DEL dbSNP153 26..34 33 - - - Human_RBP_ID_12855664 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 22926 RMVar_ID_22926 Human_SNP_ID_614043639 A-to-I Human chr16 + 89519602 89519602 89519602 TGGGGTTTCTGCATGTTGGTCAGGCTTGTCTCAGACTCCCGACCTCAGGTGATGCACCCGCCTCA TGGGGTTTCTGCATGTTGGTCAGGCTTGTCTCGGACTCCCGACCTCAGGTGATGCACCCGCCTCA A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs12050940 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8442948,Human_RBP_ID_12855669 Clinvar_Rec_87,Clinvar_Rec_88 GWAS_ID_2174,GWAS_ID_2175,GWAS_ID_2176,GWAS_ID_2177,GWAS_ID_2178,GWAS_ID_2179,GWAS_ID_2180,GWAS_ID_2181,GWAS_ID_2182,GWAS_ID_2183,GWAS_ID_2184,GWAS_ID_2185,GWAS_ID_2186,GWAS_ID_2187,GWAS_ID_2188,GWAS_ID_2189,GWAS_ID_2190,GWAS_ID_2191,GWAS_ID_2192,GWAS_ID_2193,GWAS_ID_2194,GWAS_ID_2195,GWAS_ID_2196,GWAS_ID_2197,GWAS_ID_2198,GWAS_ID_2199,GWAS_ID_2200,GWAS_ID_2201,GWAS_ID_2202,GWAS_ID_2203,GWAS_ID_2204,GWAS_ID_2205,GWAS_ID_2206,GWAS_ID_2207,GWAS_ID_2208,GWAS_ID_2209,GWAS_ID_2210,GWAS_ID_2211,GWAS_ID_2212,GWAS_ID_2213,GWAS_ID_2214,GWAS_ID_2215,GWAS_ID_2216,GWAS_ID_2217,GWAS_ID_2218,GWAS_ID_2219,GWAS_ID_2220,GWAS_ID_2221,GWAS_ID_2222,GWAS_ID_2223,GWAS_ID_2224,GWAS_ID_2225,GWAS_ID_2226,GWAS_ID_2227,GWAS_ID_2228,GWAS_ID_2229,GWAS_ID_2230,GWAS_ID_2231,GWAS_ID_2232,GWAS_ID_2233 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 22927 RMVar_ID_22927 Human_SNP_ID_614043640 A-to-I Human chr16 + 89519602 89519602 89519602 TGGGGTTTCTGCATGTTGGTCAGGCTTGTCTCAGACTCCCGACCTCAGGTGATGCACCCGCCTCA TGGGGTTTCTGCATGTTGGTCAGGCTTGTCTCTGACTCCCGACCTCAGGTGATGCACCCGCCTCA A T SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs12050940 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8442948,Human_RBP_ID_12855669 Clinvar_Rec_87,Clinvar_Rec_88 GWAS_ID_2174,GWAS_ID_2175,GWAS_ID_2176,GWAS_ID_2177,GWAS_ID_2178,GWAS_ID_2179,GWAS_ID_2180,GWAS_ID_2181,GWAS_ID_2182,GWAS_ID_2183,GWAS_ID_2184,GWAS_ID_2185,GWAS_ID_2186,GWAS_ID_2187,GWAS_ID_2188,GWAS_ID_2189,GWAS_ID_2190,GWAS_ID_2191,GWAS_ID_2192,GWAS_ID_2193,GWAS_ID_2194,GWAS_ID_2195,GWAS_ID_2196,GWAS_ID_2197,GWAS_ID_2198,GWAS_ID_2199,GWAS_ID_2200,GWAS_ID_2201,GWAS_ID_2202,GWAS_ID_2203,GWAS_ID_2204,GWAS_ID_2205,GWAS_ID_2206,GWAS_ID_2207,GWAS_ID_2208,GWAS_ID_2209,GWAS_ID_2210,GWAS_ID_2211,GWAS_ID_2212,GWAS_ID_2213,GWAS_ID_2214,GWAS_ID_2215,GWAS_ID_2216,GWAS_ID_2217,GWAS_ID_2218,GWAS_ID_2219,GWAS_ID_2220,GWAS_ID_2221,GWAS_ID_2222,GWAS_ID_2223,GWAS_ID_2224,GWAS_ID_2225,GWAS_ID_2226,GWAS_ID_2227,GWAS_ID_2228,GWAS_ID_2229,GWAS_ID_2230,GWAS_ID_2231,GWAS_ID_2232,GWAS_ID_2233 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 22928 RMVar_ID_22928 Human_SNP_ID_614043912 A-to-I Human chr16 + 89520420 89520420 89520420 GTTTGTTTGTTTGTTTGTTTGTTTTGAGATGGAGTTTCACTCTTCGTTGCCCAGGCAGGAGTGAA GTTTGTTTGTTTGTTTGTTTGTTTTGAGATGGCGTTTCACTCTTCGTTGCCCAGGCAGGAGTGAA A C SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs543001922 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12855720,Human_RBP_ID_22207732,Human_RBP_ID_26952718 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 22929 RMVar_ID_22929 Human_SNP_ID_614043913 A-to-I Human chr16 + 89520420 89520420 89520420 GTTTGTTTGTTTGTTTGTTTGTTTTGAGATGGAGTTTCACTCTTCGTTGCCCAGGCAGGAGTGAA GTTTGTTTGTTTGTTTGTTTGTTTTGAGATGGGGTTTCACTCTTCGTTGCCCAGGCAGGAGTGAA A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs543001922 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12855720,Human_RBP_ID_22207732,Human_RBP_ID_26952718 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 22930 RMVar_ID_22930 Human_SNP_ID_614043966 A-to-I Human chr16 + 89520523 89520523 89520523 TGTTTAAGCGATTCTCCTGCGTTAGCCTCCCTAGTAGCTGGGCTTACAGGCGCGTGGTACCACGC TGTTTAAGCGATTCTCCTGCGTTAGCCTCCCTGGTAGCTGGGCTTACAGGCGCGTGGTACCACGC A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs904517179 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12855725 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 22931 RMVar_ID_22931 Human_SNP_ID_614043981 A-to-I Human chr16 + 89520552 89520552 89520552 CCTAGTAGCTGGGCTTACAGGCGCGTGGTACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGA CCTAGTAGCTGGGCTTACAGGCGCGTGGTACCGCGCCCAGCTAATTTTTGTATTTTTAGTAGAGA A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1437610357 Functional Loss SNV dbSNP153 33..33 33 - - - 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 22932 RMVar_ID_22932 Human_SNP_ID_614044009 A-to-I Human chr16 + 89520631 89520631 89520631 GTTGGCCAGGCTGGTGTTGAACTCCTGACCTCAGGTGATCCACTCACCTCAGCCTCCCAAAGTGC GTTGGCCAGGCTGGTGTTGAACTCCTGACCTCCGGTGATCCACTCACCTCAGCCTCCCAAAGTGC A C SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1004214076 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12855730,Human_RBP_ID_25237100 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 22933 RMVar_ID_22933 Human_SNP_ID_614044292 A-to-I Human chr16 + 89521485 89521485 89521485 ATTAGAAATTATTTGGGATTTGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCTGAGGTGGGA ATTAGAAATTATTTGGGATTTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGA A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1364404905 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25247317 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 22934 RMVar_ID_22934 Human_SNP_ID_614044308 A-to-I Human chr16 + 89521578 89521575 89521578 TGCCTTGGCAACATAGTGAGACCTCATCTTCTACTCAAATTTAAAAAATTAGCCGGGCGCAGTGG TGCCTTGGCAACATAGTGAGACCTCATCTT___CTCAAATTTAAAAAATTAGCCGGGCGCAGTGG TCTA T SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1380981097 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_5440997,Human_RBP_ID_12855807,Human_RBP_ID_22207741,Human_RBP_ID_23274444,Human_RBP_ID_26952743 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 22935 RMVar_ID_22935 Human_SNP_ID_614044309 A-to-I Human chr16 + 89521578 89521578 89521578 TGCCTTGGCAACATAGTGAGACCTCATCTTCTACTCAAATTTAAAAAATTAGCCGGGCGCAGTGG TGCCTTGGCAACATAGTGAGACCTCATCTTCTGCTCAAATTTAAAAAATTAGCCGGGCGCAGTGG A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1222016761 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5440997,Human_RBP_ID_12855807,Human_RBP_ID_22207741,Human_RBP_ID_23274444,Human_RBP_ID_26952743 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 22936 RMVar_ID_22936 Human_SNP_ID_614044329 A-to-I Human chr16 + 89521636 89521636 89521636 GCAGTGGCGTGCACCTGTACTCCCAGCTACTCAGGAGGCTCAGTTGGGAGGATCACTTGAGCCCA GCAGTGGCGTGCACCTGTACTCCCAGCTACTCGGGAGGCTCAGTTGGGAGGATCACTTGAGCCCA A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,cerebellum - 29129909,30559470 RNA-Seq:(High) rs1454982444 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26952745 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 22937 RMVar_ID_22937 Human_SNP_ID_614044454 A-to-I Human chr16 + 89522080 89522080 89522080 AGTTTCTAACAATTGGATACTCACCTGAGAACATAAATTTGCTCTCTGAAATAAGCGGTGGGCTT AGTTTCTAACAATTGGATACTCACCTGAGAACGTAAATTTGCTCTCTGAAATAAGCGGTGGGCTT A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11862081 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18687523,Human_RBP_ID_22207749,Human_RBP_ID_26952753 GWAS_ID_2234,GWAS_ID_2235,GWAS_ID_2236,GWAS_ID_2237,GWAS_ID_2238 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 22938 RMVar_ID_22938 Human_SNP_ID_614044598 A-to-I Human chr16 + 89522488 89522488 89522488 GGCGCAGGTGTTCTGGAAATGACGTCGTTACCACCGCTGGGTCTGTGGCGGTTTGTCCGCAGGCG GGCGCAGGTGTTCTGGAAATGACGTCGTTACCGCCGCTGGGTCTGTGGCGGTTTGTCCGCAGGCG A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4785687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1525793,Human_RBP_ID_23118542,Human_RBP_ID_27447457 GWAS_ID_2239,GWAS_ID_2240,GWAS_ID_2241,GWAS_ID_2242 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 22939 RMVar_ID_22939 Human_SNP_ID_614045006 A-to-I Human chr16 + 89523605 89523605 89523605 ACGGCCTGGGACGGTCGTTTCTTTTCTGAGACAGGGTCGTTCTCTGTCACCCAGGCTGGAGCACA ACGGCCTGGGACGGTCGTTTCTTTTCTGAGACGGGGTCGTTCTCTGTCACCCAGGCTGGAGCACA A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs573477032 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_45835,Human_RBP_ID_1847949,Human_RBP_ID_22052318,Human_RBP_ID_22207763,Human_RBP_ID_23118685,Human_RBP_ID_24414478,Human_RBP_ID_25237156 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 22940 RMVar_ID_22940 Human_SNP_ID_614046453 A-to-I Human chr16 + 89527330 89527330 89527330 CGCTTCTGAATTCACATTCTTGTATAATTTTCACTGACTGTGCTCTTTGATGAAAGCTTCCCAAA CGCTTCTGAATTCACATTCTTGTATAATTTTCCCTGACTGTGCTCTTTGATGAAAGCTTCCCAAA A C SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs889037145 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23707501 RMVar_hsa_circ_29778,RMVar_hsa_circ_111094,RMVar_hsa_circ_100230,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,RMVar_hsa_circ_308162,RMVar_hsa_circ_343883,RMVar_hsa_circ_35388,RMVar_hsa_circ_8491,RMVar_hsa_circ_106819,RMVar_hsa_circ_180625,RMVar_hsa_circ_39571,RMVar_hsa_circ_180626 22941 RMVar_ID_22941 Human_SNP_ID_614047112 A-to-I Human chr16 + 89529080 89529080 89529080 GTGATTCACCCGCCACGGCCTCCCAAAGTGCTAGGATTACAGGCGTGAGCCACCGCGCCCGGCCT GTGATTCACCCGCCACGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCCCGGCCT A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1429596990 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29778,RMVar_hsa_circ_111094,RMVar_hsa_circ_100230,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,RMVar_hsa_circ_308162,RMVar_hsa_circ_343883,RMVar_hsa_circ_35388,RMVar_hsa_circ_8491,RMVar_hsa_circ_106819,RMVar_hsa_circ_180625,RMVar_hsa_circ_39571,RMVar_hsa_circ_180626 22942 RMVar_ID_22942 Human_SNP_ID_614047154 A-to-I Human chr16 + 89529200 89529200 89529200 TTACATTTGAAAACAAAATATACTGAAAATAGAAAAACCTGAACGTTGTTATTGTCACAAGGCTG TTACATTTGAAAACAAAATATACTGAAAATAGGAAAACCTGAACGTTGTTATTGTCACAAGGCTG A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs370200624 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1751548,Human_Splice_Rec_1751780,Human_Splice_Rec_1751960,Human_Splice_Rec_1752144 RMVar_hsa_circ_29778,RMVar_hsa_circ_111094,RMVar_hsa_circ_100230,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,RMVar_hsa_circ_308162,RMVar_hsa_circ_343883,RMVar_hsa_circ_35388,RMVar_hsa_circ_8491,RMVar_hsa_circ_106819,RMVar_hsa_circ_180625,RMVar_hsa_circ_39571,RMVar_hsa_circ_180626 22943 RMVar_ID_22943 Human_SNP_ID_614047160 A-to-I Human chr16 + 89529209 89529209 89529209 AAAACAAAATATACTGAAAATAGAAAAACCTGAACGTTGTTATTGTCACAAGGCTGGCTAGATCT AAAACAAAATATACTGAAAATAGAAAAACCTGCACGTTGTTATTGTCACAAGGCTGGCTAGATCT A C SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017991641 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1751548,Human_Splice_Rec_1751780,Human_Splice_Rec_1751960,Human_Splice_Rec_1752144 RMVar_hsa_circ_29778,RMVar_hsa_circ_111094,RMVar_hsa_circ_100230,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,RMVar_hsa_circ_308162,RMVar_hsa_circ_343883,RMVar_hsa_circ_35388,RMVar_hsa_circ_8491,RMVar_hsa_circ_106819,RMVar_hsa_circ_180625,RMVar_hsa_circ_39571,RMVar_hsa_circ_180626 22944 RMVar_ID_22944 Human_SNP_ID_614047161 A-to-I Human chr16 + 89529209 89529209 89529209 AAAACAAAATATACTGAAAATAGAAAAACCTGAACGTTGTTATTGTCACAAGGCTGGCTAGATCT AAAACAAAATATACTGAAAATAGAAAAACCTGGACGTTGTTATTGTCACAAGGCTGGCTAGATCT A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017991641 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1751548,Human_Splice_Rec_1751780,Human_Splice_Rec_1751960,Human_Splice_Rec_1752144 RMVar_hsa_circ_29778,RMVar_hsa_circ_111094,RMVar_hsa_circ_100230,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,RMVar_hsa_circ_308162,RMVar_hsa_circ_343883,RMVar_hsa_circ_35388,RMVar_hsa_circ_8491,RMVar_hsa_circ_106819,RMVar_hsa_circ_180625,RMVar_hsa_circ_39571,RMVar_hsa_circ_180626 22945 RMVar_ID_22945 Human_SNP_ID_614048746 A-to-I Human chr16 + 89532850 89532850 89532850 TCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGACAGGCGGATCACCAGAGGTCAGGATTTCA TCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGACAGGCGGATCACCAGAGGTCAGGATTTCA A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs562864097 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 22946 RMVar_ID_22946 Human_SNP_ID_614048769 A-to-I Human chr16 + 89532913 89532913 89532913 CATGAGCAGCCTGGCCAACATGCTGAAACCCCATCTCTACAAAAATACAAAAGTCAGCCGGGTGT CATGAGCAGCCTGGCCAACATGCTGAAACCCCGTCTCTACAAAAATACAAAAGTCAGCCGGGTGT A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs992657284 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 22947 RMVar_ID_22947 Human_SNP_ID_614048953 A-to-I Human chr16 + 89533352 89533352 89533352 ACCACGCCTGGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGG ACCACGCCTGGCTAATTTTTTGTATTTTTAGTGGAGACGGGGTTTCACCGTGTTAGCCAGGATGG A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1156737276 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 22948 RMVar_ID_22948 Human_SNP_ID_614050613 A-to-I Human chr16 + 89537555 89537554 89537556 TTTATGCTTCGACTTTTTTTTTCTTCAGAGACAGGGTGTCGTTCTGTCGCCCAGGCTGGAGTGCA TTTATGCTTCGACTTTTTTTTTCTTCAGAGAC__GGTGTCGTTCTGTCGCCCAGGCTGGAGTGCA CAG C SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1162200489 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_45857,Human_RBP_ID_3501739,Human_RBP_ID_26952816 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 22949 RMVar_ID_22949 Human_SNP_ID_614050616 A-to-I Human chr16 + 89537555 89537555 89537555 TTTATGCTTCGACTTTTTTTTTCTTCAGAGACAGGGTGTCGTTCTGTCGCCCAGGCTGGAGTGCA TTTATGCTTCGACTTTTTTTTTCTTCAGAGACCGGGTGTCGTTCTGTCGCCCAGGCTGGAGTGCA A C SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1462524850 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_45857,Human_RBP_ID_3501739,Human_RBP_ID_26952816 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 22950 RMVar_ID_22950 Human_SNP_ID_614055136 A-to-I Human chr16 + 89549508 89549507 89549509 CAGCAAGACCCCATCTCTTAAAAGAAAAGAATAAAGAGTATTAGCCAGGCATGGTGGTGGAGCAC CAGCAAGACCCCATCTCTTAAAAGAAAAGAAT__AGAGTATTAGCCAGGCATGGTGGTGGAGCAC TAA T SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs905298803 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_22207855 Human_Splice_Rec_1752618 RMVar_hsa_circ_29778,RMVar_hsa_circ_112642,RMVar_hsa_circ_180624,RMVar_hsa_circ_35388,RMVar_hsa_circ_106819,RMVar_hsa_circ_180626,RMVar_hsa_circ_306711,RMVar_hsa_circ_93099,RMVar_hsa_circ_180634,RMVar_hsa_circ_275214,RMVar_hsa_circ_114472,RMVar_hsa_circ_180637,RMVar_hsa_circ_306888,RMVar_hsa_circ_180640,RMVar_hsa_circ_103409,RMVar_hsa_circ_180642,RMVar_hsa_circ_180643 22951 RMVar_ID_22951 Human_SNP_ID_614055159 A-to-I Human chr16 + 89549571 89549571 89549571 ACACCTCTGGTCTCAGCTACTCAGGAGGCTGCAGCAGGAGGATTGCTTGAACCTGGGAGGTTGAA ACACCTCTGGTCTCAGCTACTCAGGAGGCTGCGGCAGGAGGATTGCTTGAACCTGGGAGGTTGAA A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs912673546 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17564479 Human_Splice_Rec_1752618 RMVar_hsa_circ_29778,RMVar_hsa_circ_112642,RMVar_hsa_circ_180624,RMVar_hsa_circ_35388,RMVar_hsa_circ_106819,RMVar_hsa_circ_180626,RMVar_hsa_circ_306711,RMVar_hsa_circ_93099,RMVar_hsa_circ_180634,RMVar_hsa_circ_275214,RMVar_hsa_circ_114472,RMVar_hsa_circ_180637,RMVar_hsa_circ_306888,RMVar_hsa_circ_180640,RMVar_hsa_circ_103409,RMVar_hsa_circ_180642,RMVar_hsa_circ_180643 22952 RMVar_ID_22952 Human_SNP_ID_614055161 A-to-I Human chr16 + 89549574 89549574 89549574 CCTCTGGTCTCAGCTACTCAGGAGGCTGCAGCAGGAGGATTGCTTGAACCTGGGAGGTTGAAGCA CCTCTGGTCTCAGCTACTCAGGAGGCTGCAGCGGGAGGATTGCTTGAACCTGGGAGGTTGAAGCA A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 29129909,30559470 RNA-Seq:(High) rs1346190698 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17564479 Human_Splice_Rec_1752618 RMVar_hsa_circ_29778,RMVar_hsa_circ_112642,RMVar_hsa_circ_180624,RMVar_hsa_circ_35388,RMVar_hsa_circ_106819,RMVar_hsa_circ_180626,RMVar_hsa_circ_306711,RMVar_hsa_circ_93099,RMVar_hsa_circ_180634,RMVar_hsa_circ_275214,RMVar_hsa_circ_114472,RMVar_hsa_circ_180637,RMVar_hsa_circ_306888,RMVar_hsa_circ_180640,RMVar_hsa_circ_103409,RMVar_hsa_circ_180642,RMVar_hsa_circ_180643 22953 RMVar_ID_22953 Human_SNP_ID_614055411 A-to-I Human chr16 + 89550252 89550252 89550252 TGGAGTGCAGTGGCATGATCTTGCCCTACTGTAACCTCCGTCTCTCAGGTTCAAGTGATTCTCTT TGGAGTGCAGTGGCATGATCTTGCCCTACTGTGACCTCCGTCTCTCAGGTTCAAGTGATTCTCTT A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1351707207 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12856522 RMVar_hsa_circ_29778,RMVar_hsa_circ_112642,RMVar_hsa_circ_180624,RMVar_hsa_circ_35388,RMVar_hsa_circ_106819,RMVar_hsa_circ_180626,RMVar_hsa_circ_306711,RMVar_hsa_circ_93099,RMVar_hsa_circ_180634,RMVar_hsa_circ_275214,RMVar_hsa_circ_114472,RMVar_hsa_circ_180637,RMVar_hsa_circ_306888,RMVar_hsa_circ_180640,RMVar_hsa_circ_103409,RMVar_hsa_circ_180642,RMVar_hsa_circ_180643 22954 RMVar_ID_22954 Human_SNP_ID_614058281 A-to-I Human chr16 + 89558271 89558271 89558271 TTTTGGCAGAGTCTTGCTCTGTCGCCCAGGCTAGAGTGCAGTGGCGCCATCTCGGCTCACTGCAG TTTTGGCAGAGTCTTGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCCATCTCGGCTCACTGCAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474309951 Functional Loss SNV dbSNP153 33..33 33 - - - 22955 RMVar_ID_22955 Human_SNP_ID_614061020 A-to-I Human chr16 + 89563968 89563967 89563969 CATTGTTCTTGCTTCATGGACAAGAGGCAGCCAGAGAGAGTGCCAGGGTGCCCTGGTCTGAGCTG CATTGTTCTTGCTTCATGGACAAGAGGCAGCC__AGAGAGTGCCAGGGTGCCCTGGTCTGAGCTG CAG C RPL13 Ensembl:ENSG00000167526 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs956738571 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_1525882,Human_RBP_ID_8443024,Human_RBP_ID_12856765 Human_miRNA_ID_335889,Human_miRNA_ID_955285,Human_miRNA_ID_2332803,Human_miRNA_ID_2965886 RMVar_hsa_circ_120915,RMVar_hsa_circ_180652 22956 RMVar_ID_22956 Human_SNP_ID_614061022 A-to-I Human chr16 + 89563968 89563968 89563968 CATTGTTCTTGCTTCATGGACAAGAGGCAGCCAGAGAGAGTGCCAGGGTGCCCTGGTCTGAGCTG CATTGTTCTTGCTTCATGGACAAGAGGCAGCCGGAGAGAGTGCCAGGGTGCCCTGGTCTGAGCTG A G RPL13 Ensembl:ENSG00000167526 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1465081809 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1525882,Human_RBP_ID_8443024,Human_RBP_ID_12856765 Human_miRNA_ID_335889,Human_miRNA_ID_955285,Human_miRNA_ID_2332803,Human_miRNA_ID_2965886 RMVar_hsa_circ_120915,RMVar_hsa_circ_180652 22957 RMVar_ID_22957 Human_SNP_ID_614066876 A-to-I Human chr16 + 89579035 89579035 89579035 TTTACAGGCCGGGCACGGTGGCTCACGCCTGTAATCGCAGCACTTTGGAAGTCCGAGGTGGGGGG TTTACAGGCCGGGCACGGTGGCTCACGCCTGTGATCGCAGCACTTTGGAAGTCCGAGGTGGGGGG A G CPNE7 Ensembl:ENSG00000178773 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1378049851 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22370130 RMVar_hsa_circ_110987,RMVar_hsa_circ_180655 22958 RMVar_ID_22958 Human_SNP_ID_614066898 A-to-I Human chr16 + 89579079 89579079 89579079 TTGGAAGTCCGAGGTGGGGGGATCACGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGATGA TTGGAAGTCCGAGGTGGGGGGATCACGAGGTCCGGAGTTCGAGACCAGCCTGGCCAACATGATGA A C CPNE7 Ensembl:ENSG00000178773 Protein coding intron GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831 HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line - 29129909,32596459 RNA-Seq:(High) rs886181582 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110987,RMVar_hsa_circ_180655 22959 RMVar_ID_22959 Human_SNP_ID_614066899 A-to-I Human chr16 + 89579079 89579079 89579079 TTGGAAGTCCGAGGTGGGGGGATCACGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGATGA TTGGAAGTCCGAGGTGGGGGGATCACGAGGTCGGGAGTTCGAGACCAGCCTGGCCAACATGATGA A G CPNE7 Ensembl:ENSG00000178773 Protein coding intron GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831 HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line - 29129909,32596459 RNA-Seq:(High) rs886181582 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110987,RMVar_hsa_circ_180655 22960 RMVar_ID_22960 Human_SNP_ID_614066926 A-to-I Human chr16 + 89579171 89579171 89579171 GAAATTAGCCAGGCGTGGTGGTGCGTGCCTGTAGTCCCAGCTACTGGGGAGGCTGAGGCAGGAGA GAAATTAGCCAGGCGTGGTGGTGCGTGCCTGTTGTCCCAGCTACTGGGGAGGCTGAGGCAGGAGA A T CPNE7 Ensembl:ENSG00000178773 Protein coding intron GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs1348187115 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110987,RMVar_hsa_circ_180655 22961 RMVar_ID_22961 Human_SNP_ID_614066935 A-to-I Human chr16 + 89579212 89579212 89579212 TACTGGGGAGGCTGAGGCAGGAGAATCACTTGAACCTGGGAGGCAGAGGTTTCAGCGAGCCGAGA TACTGGGGAGGCTGAGGCAGGAGAATCACTTGCACCTGGGAGGCAGAGGTTTCAGCGAGCCGAGA A C CPNE7 Ensembl:ENSG00000178773 Protein coding intron GSE123020:GSM3490829,GSM3490830,GSM3490831 esophageal squamous carcinoma cells,EC109 cell line - 32596459 RNA-Seq:(High) rs925081797 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110987,RMVar_hsa_circ_180655 22962 RMVar_ID_22962 Human_SNP_ID_614098442 A-to-I Human chr16 - 89650271 89650271 89650271 GGAAGGCTGAGGCGGGAGAATTGCTTGAGCCCAGGAGGTGGAGGTTGCAGTGAGCCGAGATCACA GGAAGGCTGAGGCGGGAGAATTGCTTGAGCCCCGGAGGTGGAGGTTGCAGTGAGCCGAGATCACA T G CHMP1A Ensembl:ENSG00000131165 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1209095514 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126095,RMVar_hsa_circ_180665,RMVar_hsa_circ_106777,RMVar_hsa_circ_180667 22963 RMVar_ID_22963 Human_SNP_ID_614098713 A-to-I Human chr16 - 89651195 89651195 89651195 TTTTAATTTTTTTGTAGAGATGGGGTTTCGCCATGTTGGCCAGGCCGGTCTCGAACTCTTATCCT TTTTAATTTTTTTGTAGAGATGGGGTTTCGCCCTGTTGGCCAGGCCGGTCTCGAACTCTTATCCT T G CHMP1A Ensembl:ENSG00000131165 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1208405585 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126095,RMVar_hsa_circ_180665,RMVar_hsa_circ_106777,RMVar_hsa_circ_180667 22964 RMVar_ID_22964 Human_SNP_ID_614099492 A-to-I Human chr16 - 89653474 89653474 89653474 GGACTACAGGCGCCCACCACCATGCCCAGCTAATTTTTTTTTACATTTTTAATAGAGACGGGGTT GGACTACAGGCGCCCACCACCATGCCCAGCTACTTTTTTTTTACATTTTTAATAGAGACGGGGTT T G CHMP1A Ensembl:ENSG00000131165 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1403615340 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126095,RMVar_hsa_circ_180665 22965 RMVar_ID_22965 Human_SNP_ID_614104249 A-to-I Human chr16 + 89665108 89665107 89665108 CTCTTGACGTTCTGGGCTCAAACGATTCTCCCACCTCAGCTCCCTGAGTAGCTGGGGCCACAGTG CTCTTGACGTTCTGGGCTCAAACGATTCTCCC_CCTCAGCTCCCTGAGTAGCTGGGGCCACAGTG CA C SPATA33 Ensembl:ENSG00000167523 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334033594 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_6547752 22966 RMVar_ID_22966 Human_SNP_ID_614104255 A-to-I Human chr16 + 89665135 89665135 89665135 CTCCCACCTCAGCTCCCTGAGTAGCTGGGGCCACAGTGCACGCCACCACCCCCAGCTATTTTTTG CTCCCACCTCAGCTCCCTGAGTAGCTGGGGCCGCAGTGCACGCCACCACCCCCAGCTATTTTTTG A G SPATA33 Ensembl:ENSG00000167523 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1406271501 Functional Loss SNV dbSNP153 33..33 33 - - - 22967 RMVar_ID_22967 Human_SNP_ID_614111650 A-to-I Human chr16 - 89684492 89684492 89684492 CAAAAAAAAAAGAAAATGCAGGTGTTGTGACCAGGCACAGTGGCTCATGCCTATAATCCCAACAC CAAAAAAAAAAGAAAATGCAGGTGTTGTGACCCGGCACAGTGGCTCATGCCTATAATCCCAACAC T G LINC02166 Ensembl:ENSG00000260259 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432882278 Functional Loss SNV dbSNP153 33..33 33 - - - 22968 RMVar_ID_22968 Human_SNP_ID_614113187 A-to-I Human chr16 + 89687583 89687583 89687583 GAGTTGGCCTTTTCTTTTTTGTTGTTTTTTTGAGACAGGGTCTAGCGCTCTCGCCCAGGCTGGAA GAGTTGGCCTTTTCTTTTTTGTTGTTTTTTTGGGACAGGGTCTAGCGCTCTCGCCCAGGCTGGAA A G CDK10 Ensembl:ENSG00000185324 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1211466757 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12857718,Human_RBP_ID_26952993 22969 RMVar_ID_22969 Human_SNP_ID_614113336 A-to-I Human chr16 + 89687950 89687950 89687950 CAGACTGAGGACAAATGCGGCCAGTGGCTCACACCTGTAATCTCAGCAATCTGGGAGGCTGAGGT CAGACTGAGGACAAATGCGGCCAGTGGCTCACGCCTGTAATCTCAGCAATCTGGGAGGCTGAGGT A G CDK10 Ensembl:ENSG00000185324 Protein coding intron GSE38233;GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,32596459 RNA-Seq:(High) rs1414735962 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12857733 22970 RMVar_ID_22970 Human_SNP_ID_614113341 A-to-I Human chr16 + 89687956 89687955 89687956 GAGGACAAATGCGGCCAGTGGCTCACACCTGTAATCTCAGCAATCTGGGAGGCTGAGGTGGGAGG GAGGACAAATGCGGCCAGTGGCTCACACCTGT_ATCTCAGCAATCTGGGAGGCTGAGGTGGGAGG TA T CDK10 Ensembl:ENSG00000185324 Protein coding intron GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs1467077394 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_12857733 22971 RMVar_ID_22971 Human_SNP_ID_614113498 A-to-I Human chr16 + 89688289 89688289 89688289 TATTTTTAGTAGAGACGGAGTTTCACCGTGTTAGTCAGGGTGCTCTAGATCTCCTGACTTCGTGA TATTTTTAGTAGAGACGGAGTTTCACCGTGTTCGTCAGGGTGCTCTAGATCTCCTGACTTCGTGA A C CDK10 Ensembl:ENSG00000185324 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,31158229,32596459 RNA-Seq:(High) rs1324562446 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12857744 22972 RMVar_ID_22972 Human_SNP_ID_614113685 A-to-I Human chr16 + 89688815 89688815 89688815 ATCGTCACCACCTTTTCTCATCAGAAAAGCCCAAGAGGCCGGGTACGGTGGCTCACGCTTGTAAT ATCGTCACCACCTTTTCTCATCAGAAAAGCCCCAGAGGCCGGGTACGGTGGCTCACGCTTGTAAT A C CDK10 Ensembl:ENSG00000185324 Protein coding intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs976970592 Functional Loss SNV dbSNP153 33..33 33 - - - 22973 RMVar_ID_22973 Human_SNP_ID_614113686 A-to-I Human chr16 + 89688815 89688815 89688815 ATCGTCACCACCTTTTCTCATCAGAAAAGCCCAAGAGGCCGGGTACGGTGGCTCACGCTTGTAAT ATCGTCACCACCTTTTCTCATCAGAAAAGCCCTAGAGGCCGGGTACGGTGGCTCACGCTTGTAAT A T CDK10 Ensembl:ENSG00000185324 Protein coding intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs976970592 Functional Loss SNV dbSNP153 33..33 33 - - - 22974 RMVar_ID_22974 Human_SNP_ID_614113762 A-to-I Human chr16 + 89689082 89689082 89689082 TGTTCTTGCCACTGCACTCCAGCCTGGGCAACAGAGCGAGACTCAGTCTCAAAAAAAGAAAAAAA TGTTCTTGCCACTGCACTCCAGCCTGGGCAACGGAGCGAGACTCAGTCTCAAAAAAAGAAAAAAA A G CDK10 Ensembl:ENSG00000185324 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs988264210 Functional Loss SNV dbSNP153 33..33 33 - - - 22975 RMVar_ID_22975 Human_SNP_ID_614113763 A-to-I Human chr16 + 89689084 89689084 89689084 TTCTTGCCACTGCACTCCAGCCTGGGCAACAGAGCGAGACTCAGTCTCAAAAAAAGAAAAAAAAA TTCTTGCCACTGCACTCCAGCCTGGGCAACAGTGCGAGACTCAGTCTCAAAAAAAGAAAAAAAAA A T CDK10 Ensembl:ENSG00000185324 Protein coding intron GSE38233;GSE100210;GSE99789 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 24183664,29129909,29796672 RNA-Seq:(High) rs1022047387 Functional Loss SNV dbSNP153 33..33 33 - - - 22976 RMVar_ID_22976 Human_SNP_ID_614114024 A-to-I Human chr16 + 89689720 89689720 89689720 TTTTTGTTTGTTTTTGAGATGGGTCTTGCTCTATTGCCCAGACTGGAGTGCAGTGGCATGATCAT TTTTTGTTTGTTTTTGAGATGGGTCTTGCTCTCTTGCCCAGACTGGAGTGCAGTGGCATGATCAT A C CDK10 Ensembl:ENSG00000185324 Protein coding intron GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs903804669 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 22977 RMVar_ID_22977 Human_SNP_ID_614114025 A-to-I Human chr16 + 89689720 89689720 89689720 TTTTTGTTTGTTTTTGAGATGGGTCTTGCTCTATTGCCCAGACTGGAGTGCAGTGGCATGATCAT TTTTTGTTTGTTTTTGAGATGGGTCTTGCTCTGTTGCCCAGACTGGAGTGCAGTGGCATGATCAT A G CDK10 Ensembl:ENSG00000185324 Protein coding intron GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs903804669 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 22978 RMVar_ID_22978 Human_SNP_ID_614114088 A-to-I Human chr16 + 89689945 89689945 89689945 GGCTCAAATGATCCTCCTGCCTCGGCCTCCCAAAGCACTGGGATTACAGGTGTGAGCCACTGCAC GGCTCAAATGATCCTCCTGCCTCGGCCTCCCAGAGCACTGGGATTACAGGTGTGAGCCACTGCAC A G CDK10 Ensembl:ENSG00000185324 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs998718403 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 22979 RMVar_ID_22979 Human_SNP_ID_614114113 A-to-I Human chr16 + 89690047 89690046 89690048 TGATCACGCCACTGCACCCCAGCCTTGGCAACAGAGTGAGACCCTGTCTCAAAAAAACCAAAAAC TGATCACGCCACTGCACCCCAGCCTTGGCAAC__AGTGAGACCCTGTCTCAAAAAAACCAAAAAC CAG C CDK10 Ensembl:ENSG00000185324 Protein coding intron GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs1017027399 Functional Loss DEL dbSNP153 33..34 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 22980 RMVar_ID_22980 Human_SNP_ID_614129322 A-to-I Human chr16 + 89724445 89724445 89724445 GAGGTGGGTGGATCACTTGAGGTCACGAGATCAAGACCAACCTGGCCAACATAGCGAAACCCCAT GAGGTGGGTGGATCACTTGAGGTCACGAGATCGAGACCAACCTGGCCAACATAGCGAAACCCCAT A G ZNF276 Ensembl:ENSG00000158805 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs915368092 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117800,RMVar_hsa_circ_24329,RMVar_hsa_circ_53207,RMVar_hsa_circ_180681 22981 RMVar_ID_22981 Human_SNP_ID_614133903 A-to-I Human chr16 - 89734554 89734554 89734554 TGCACTTTGGAAGGCTGAGATCACTTGAGGTCAGGAGTTAGAGATCACCCTGGCCAACATGGTGA TGCACTTTGGAAGGCTGAGATCACTTGAGGTCTGGAGTTAGAGATCACCCTGGCCAACATGGTGA T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388847197 Functional Loss SNV dbSNP153 33..33 33 - - - 22982 RMVar_ID_22982 Human_SNP_ID_614134099 A-to-I Human chr16 - 89735035 89735035 89735035 TCCACCTCCGCCTCCCAAGTAGCTGTGCCTACAGGCGTGTGCCACCACACCCAGATAATTTTTGT TCCACCTCCGCCTCCCAAGTAGCTGTGCCTACCGGCGTGTGCCACCACACCCAGATAATTTTTGT T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1207241772 Functional Loss SNV dbSNP153 33..33 33 - - - 22983 RMVar_ID_22983 Human_SNP_ID_614134624 A-to-I Human chr16 - 89736039 89736039 89736039 AAAATACGAAAAATTAGTTGGGTGTGGTGGCCAGCACCTGTAGTCCCAGCTATTTGGGAGGCTGA AAAATACGAAAAATTAGTTGGGTGTGGTGGCCGGCACCTGTAGTCCCAGCTATTTGGGAGGCTGA T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1293030291 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23166152,Human_RBP_ID_26444457 22984 RMVar_ID_22984 Human_SNP_ID_614134715 A-to-I Human chr16 - 89736254 89736254 89736254 GGGAGGCCAAGGCAGGCAAATCACCTGAGGTCAGGAACTCGAGACCAGCCTGGCCAACATAGCAA GGGAGGCCAAGGCAGGCAAATCACCTGAGGTCTGGAACTCGAGACCAGCCTGGCCAACATAGCAA T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1402786206 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12858724 22985 RMVar_ID_22985 Human_SNP_ID_614134828 A-to-I Human chr16 - 89736463 89736463 89736463 AAAATTAGCCAGGTGTGGTGGCACACACCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGCAGA AAAATTAGCCAGGTGTGGTGGCACACACCTGTGGTCCCAGCTACTCGGGAGGCTGAGGCAGCAGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs936797977 Functional Loss SNV dbSNP153 33..33 33 - - - 22986 RMVar_ID_22986 Human_SNP_ID_614135280 A-to-I Human chr16 - 89737421 89737421 89737421 CGCCTCCCAGGCTCAAGCGATTCTTGTGCCTCAGCCTGCCAAGTAGCTGGGATTACAGGCGCCCC CGCCTCCCAGGCTCAAGCGATTCTTGTGCCTCTGCCTGCCAAGTAGCTGGGATTACAGGCGCCCC T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs983563884 Functional Loss SNV dbSNP153 33..33 33 - - - 22987 RMVar_ID_22987 Human_SNP_ID_614135281 A-to-I Human chr16 - 89737421 89737421 89737421 CGCCTCCCAGGCTCAAGCGATTCTTGTGCCTCAGCCTGCCAAGTAGCTGGGATTACAGGCGCCCC CGCCTCCCAGGCTCAAGCGATTCTTGTGCCTCGGCCTGCCAAGTAGCTGGGATTACAGGCGCCCC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs983563884 Functional Loss SNV dbSNP153 33..33 33 - - - 22988 RMVar_ID_22988 Human_SNP_ID_614137033 A-to-I Human chr16 + 89740473 89740473 89740473 GCCTGGCAATATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCCGGGTGTGACAGACT GCCTGGCAATATGGTGAAACCCCGTCTCTACTGAAAATACAAAAATTAGCCGGGTGTGACAGACT A G ZNF276 Ensembl:ENSG00000158805 Protein coding 3'UTR GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs938178257 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27249042 22989 RMVar_ID_22989 Human_SNP_ID_614138593 A-to-I Human chr16 - 89744086 89744086 89744086 GTTTGAGACCAGCCTGGCCAACATGTGAAACAATCTCTACTGAAAATACAGAAATGAGCTGGGTG GTTTGAGACCAGCCTGGCCAACATGTGAAACAGTCTCTACTGAAAATACAGAAATGAGCTGGGTG T C FANCA Ensembl:ENSG00000187741 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1266748010 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_180690,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_104573,RMVar_hsa_circ_118985,RMVar_hsa_circ_180688,RMVar_hsa_circ_180689,RMVar_hsa_circ_277778,RMVar_hsa_circ_372580,RMVar_hsa_circ_376596,RMVar_hsa_circ_124924,RMVar_hsa_circ_108915,RMVar_hsa_circ_116326,RMVar_hsa_circ_104647,RMVar_hsa_circ_180694,RMVar_hsa_circ_180696,RMVar_hsa_circ_180697,RMVar_hsa_circ_180695,RMVar_hsa_circ_180692,RMVar_hsa_circ_180693,RMVar_hsa_circ_180691,RMVar_hsa_circ_6742,RMVar_hsa_circ_65065,RMVar_hsa_circ_50657 22990 RMVar_ID_22990 Human_SNP_ID_614140304 A-to-I Human chr16 - 89748094 89748094 89748094 CAGCCTGGGCAACATGACAAAACCCTGTTTCTACAAAAAATAGAAAAATTAGCTGGGTATGGTGG CAGCCTGGGCAACATGACAAAACCCTGTTTCTGCAAAAAATAGAAAAATTAGCTGGGTATGGTGG T C FANCA Ensembl:ENSG00000187741 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs570219438 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_180690,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_104573,RMVar_hsa_circ_118985,RMVar_hsa_circ_180688,RMVar_hsa_circ_180689,RMVar_hsa_circ_277778,RMVar_hsa_circ_372580,RMVar_hsa_circ_376596,RMVar_hsa_circ_124924,RMVar_hsa_circ_108915,RMVar_hsa_circ_116326,RMVar_hsa_circ_104647,RMVar_hsa_circ_180694,RMVar_hsa_circ_180696,RMVar_hsa_circ_180697,RMVar_hsa_circ_180695,RMVar_hsa_circ_180692,RMVar_hsa_circ_180693,RMVar_hsa_circ_180691,RMVar_hsa_circ_6742,RMVar_hsa_circ_65065,RMVar_hsa_circ_90173,RMVar_hsa_circ_269291,RMVar_hsa_circ_321202,RMVar_hsa_circ_300516,RMVar_hsa_circ_51929,RMVar_hsa_circ_180701 22991 RMVar_ID_22991 Human_SNP_ID_614141422 A-to-I Human chr16 - 89750661 89750661 89750661 TCAAACTATTCTCCTGCCTCTGCCTCCTGATTAGCTGGGATTACAGGCGCCTGCCACCACACCCA TCAAACTATTCTCCTGCCTCTGCCTCCTGATTCGCTGGGATTACAGGCGCCTGCCACCACACCCA T G FANCA Ensembl:ENSG00000187741 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1465952224 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_180690,RMVar_hsa_circ_83663,RMVar_hsa_circ_39754,RMVar_hsa_circ_113715,RMVar_hsa_circ_99932,RMVar_hsa_circ_180687,RMVar_hsa_circ_104573,RMVar_hsa_circ_118985,RMVar_hsa_circ_180688,RMVar_hsa_circ_180689,RMVar_hsa_circ_372580,RMVar_hsa_circ_124924,RMVar_hsa_circ_108915,RMVar_hsa_circ_116326,RMVar_hsa_circ_104647,RMVar_hsa_circ_180694,RMVar_hsa_circ_180696,RMVar_hsa_circ_180695,RMVar_hsa_circ_180692,RMVar_hsa_circ_180693,RMVar_hsa_circ_180691,RMVar_hsa_circ_45056,RMVar_hsa_circ_65065,RMVar_hsa_circ_90173,RMVar_hsa_circ_269291,RMVar_hsa_circ_321202,RMVar_hsa_circ_51929,RMVar_hsa_circ_180704,RMVar_hsa_circ_180701,RMVar_hsa_circ_299494,RMVar_hsa_circ_308338,RMVar_hsa_circ_287146,RMVar_hsa_circ_87558,RMVar_hsa_circ_107379,RMVar_hsa_circ_180705,RMVar_hsa_circ_180702,RMVar_hsa_circ_180703,RMVar_hsa_circ_319238,RMVar_hsa_circ_368426,RMVar_hsa_circ_84823,RMVar_hsa_circ_180709,RMVar_hsa_circ_36627,RMVar_hsa_circ_180708 22992 RMVar_ID_22992 Human_SNP_ID_614141588 A-to-I Human chr16 - 89751135 89751135 89751135 TAATCCCAGCACTTTGGGAGGCTGAGGTGGCTAGATCACTTGAGGTCAGGGGCTCAAGACCAGTT TAATCCCAGCACTTTGGGAGGCTGAGGTGGCTGGATCACTTGAGGTCAGGGGCTCAAGACCAGTT T C FANCA Ensembl:ENSG00000187741 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1482171403 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25237952 RMVar_hsa_circ_180690,RMVar_hsa_circ_83663,RMVar_hsa_circ_39754,RMVar_hsa_circ_113715,RMVar_hsa_circ_99932,RMVar_hsa_circ_180687,RMVar_hsa_circ_104573,RMVar_hsa_circ_118985,RMVar_hsa_circ_180688,RMVar_hsa_circ_180689,RMVar_hsa_circ_372580,RMVar_hsa_circ_124924,RMVar_hsa_circ_108915,RMVar_hsa_circ_116326,RMVar_hsa_circ_104647,RMVar_hsa_circ_180694,RMVar_hsa_circ_180696,RMVar_hsa_circ_180695,RMVar_hsa_circ_180692,RMVar_hsa_circ_180693,RMVar_hsa_circ_180691,RMVar_hsa_circ_45056,RMVar_hsa_circ_65065,RMVar_hsa_circ_90173,RMVar_hsa_circ_269291,RMVar_hsa_circ_321202,RMVar_hsa_circ_51929,RMVar_hsa_circ_180704,RMVar_hsa_circ_180701,RMVar_hsa_circ_299494,RMVar_hsa_circ_308338,RMVar_hsa_circ_287146,RMVar_hsa_circ_87558,RMVar_hsa_circ_107379,RMVar_hsa_circ_180705,RMVar_hsa_circ_180702,RMVar_hsa_circ_180703,RMVar_hsa_circ_319238,RMVar_hsa_circ_368426,RMVar_hsa_circ_84823,RMVar_hsa_circ_180709,RMVar_hsa_circ_36627,RMVar_hsa_circ_180708 22993 RMVar_ID_22993 Human_SNP_ID_614141652 A-to-I Human chr16 - 89751308 89751308 89751308 TTTTGTAGAGACGGAGTTTTGCCATGTTGCCCAGGCTTGTCTCGAACTCCTGGGCCCAAGTGAAC TTTTGTAGAGACGGAGTTTTGCCATGTTGCCCTGGCTTGTCTCGAACTCCTGGGCCCAAGTGAAC T A FANCA Ensembl:ENSG00000187741 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1369564476 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_180690,RMVar_hsa_circ_83663,RMVar_hsa_circ_39754,RMVar_hsa_circ_113715,RMVar_hsa_circ_99932,RMVar_hsa_circ_180687,RMVar_hsa_circ_104573,RMVar_hsa_circ_118985,RMVar_hsa_circ_180688,RMVar_hsa_circ_180689,RMVar_hsa_circ_372580,RMVar_hsa_circ_124924,RMVar_hsa_circ_108915,RMVar_hsa_circ_116326,RMVar_hsa_circ_104647,RMVar_hsa_circ_180694,RMVar_hsa_circ_180696,RMVar_hsa_circ_180695,RMVar_hsa_circ_180692,RMVar_hsa_circ_180693,RMVar_hsa_circ_180691,RMVar_hsa_circ_45056,RMVar_hsa_circ_65065,RMVar_hsa_circ_90173,RMVar_hsa_circ_269291,RMVar_hsa_circ_321202,RMVar_hsa_circ_51929,RMVar_hsa_circ_180704,RMVar_hsa_circ_180701,RMVar_hsa_circ_299494,RMVar_hsa_circ_308338,RMVar_hsa_circ_287146,RMVar_hsa_circ_87558,RMVar_hsa_circ_107379,RMVar_hsa_circ_180705,RMVar_hsa_circ_180702,RMVar_hsa_circ_180703,RMVar_hsa_circ_319238,RMVar_hsa_circ_368426,RMVar_hsa_circ_84823,RMVar_hsa_circ_180709,RMVar_hsa_circ_36627,RMVar_hsa_circ_180708 22994 RMVar_ID_22994 Human_SNP_ID_614141975 A-to-I Human chr16 - 89752065 89752065 89752065 TTAAGCCGCGTGCTATTAAGATATTTATTGCCAGGCGCGGTGGCTCACGCCTGTAATCCCAGAAC TTAAGCCGCGTGCTATTAAGATATTTATTGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGAAC T C FANCA Ensembl:ENSG00000187741 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs942699125 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_180690,RMVar_hsa_circ_83663,RMVar_hsa_circ_39754,RMVar_hsa_circ_113715,RMVar_hsa_circ_99932,RMVar_hsa_circ_180687,RMVar_hsa_circ_104573,RMVar_hsa_circ_118985,RMVar_hsa_circ_180688,RMVar_hsa_circ_180689,RMVar_hsa_circ_372580,RMVar_hsa_circ_124924,RMVar_hsa_circ_108915,RMVar_hsa_circ_116326,RMVar_hsa_circ_104647,RMVar_hsa_circ_180694,RMVar_hsa_circ_180696,RMVar_hsa_circ_180695,RMVar_hsa_circ_180692,RMVar_hsa_circ_180693,RMVar_hsa_circ_180691,RMVar_hsa_circ_45056,RMVar_hsa_circ_65065,RMVar_hsa_circ_90173,RMVar_hsa_circ_269291,RMVar_hsa_circ_321202,RMVar_hsa_circ_51929,RMVar_hsa_circ_180704,RMVar_hsa_circ_180701,RMVar_hsa_circ_299494,RMVar_hsa_circ_308338,RMVar_hsa_circ_287146,RMVar_hsa_circ_87558,RMVar_hsa_circ_107379,RMVar_hsa_circ_180705,RMVar_hsa_circ_180702,RMVar_hsa_circ_180703,RMVar_hsa_circ_319238,RMVar_hsa_circ_368426,RMVar_hsa_circ_84823,RMVar_hsa_circ_180709,RMVar_hsa_circ_36627,RMVar_hsa_circ_180708 22995 RMVar_ID_22995 Human_SNP_ID_614142772 A-to-I Human chr16 - 89753967 89753967 89753967 TGTCTGCAACCTCCGCCTTCCAGGTTCAGGCAATTCTGCTGCCTCAGCCTCCCAATAGGTGGGAT TGTCTGCAACCTCCGCCTTCCAGGTTCAGGCAGTTCTGCTGCCTCAGCCTCCCAATAGGTGGGAT T C FANCA Ensembl:ENSG00000187741 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs983739480 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_180690,RMVar_hsa_circ_83663,RMVar_hsa_circ_39754,RMVar_hsa_circ_113715,RMVar_hsa_circ_99932,RMVar_hsa_circ_180687,RMVar_hsa_circ_104573,RMVar_hsa_circ_118985,RMVar_hsa_circ_180688,RMVar_hsa_circ_180689,RMVar_hsa_circ_372580,RMVar_hsa_circ_124924,RMVar_hsa_circ_108915,RMVar_hsa_circ_116326,RMVar_hsa_circ_104647,RMVar_hsa_circ_180694,RMVar_hsa_circ_180696,RMVar_hsa_circ_180695,RMVar_hsa_circ_180692,RMVar_hsa_circ_180693,RMVar_hsa_circ_180691,RMVar_hsa_circ_45056,RMVar_hsa_circ_65065,RMVar_hsa_circ_90173,RMVar_hsa_circ_269291,RMVar_hsa_circ_321202,RMVar_hsa_circ_51929,RMVar_hsa_circ_180704,RMVar_hsa_circ_180701,RMVar_hsa_circ_299494,RMVar_hsa_circ_308338,RMVar_hsa_circ_287146,RMVar_hsa_circ_87558,RMVar_hsa_circ_107379,RMVar_hsa_circ_180705,RMVar_hsa_circ_180702,RMVar_hsa_circ_180703,RMVar_hsa_circ_319238,RMVar_hsa_circ_368426,RMVar_hsa_circ_84823,RMVar_hsa_circ_180710,RMVar_hsa_circ_289004,RMVar_hsa_circ_180709,RMVar_hsa_circ_36627,RMVar_hsa_circ_180708,RMVar_hsa_circ_291062,RMVar_hsa_circ_75868,RMVar_hsa_circ_283494,RMVar_hsa_circ_180712,RMVar_hsa_circ_180713,RMVar_hsa_circ_180711 22996 RMVar_ID_22996 Human_SNP_ID_614142988 A-to-I Human chr16 - 89754435 89754435 89754435 TCAGGAGGCAGAGGTTGCAGTGAGTTGAGATCATGCCACTGCAACTCCAGCCTGGGCGACAAGAG TCAGGAGGCAGAGGTTGCAGTGAGTTGAGATCGTGCCACTGCAACTCCAGCCTGGGCGACAAGAG T C FANCA Ensembl:ENSG00000187741 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1294240897 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25247418 RMVar_hsa_circ_180690,RMVar_hsa_circ_83663,RMVar_hsa_circ_39754,RMVar_hsa_circ_113715,RMVar_hsa_circ_99932,RMVar_hsa_circ_180687,RMVar_hsa_circ_104573,RMVar_hsa_circ_118985,RMVar_hsa_circ_180688,RMVar_hsa_circ_180689,RMVar_hsa_circ_372580,RMVar_hsa_circ_124924,RMVar_hsa_circ_108915,RMVar_hsa_circ_116326,RMVar_hsa_circ_104647,RMVar_hsa_circ_180694,RMVar_hsa_circ_180696,RMVar_hsa_circ_180695,RMVar_hsa_circ_180692,RMVar_hsa_circ_180693,RMVar_hsa_circ_180691,RMVar_hsa_circ_45056,RMVar_hsa_circ_65065,RMVar_hsa_circ_90173,RMVar_hsa_circ_269291,RMVar_hsa_circ_321202,RMVar_hsa_circ_51929,RMVar_hsa_circ_180704,RMVar_hsa_circ_180701,RMVar_hsa_circ_299494,RMVar_hsa_circ_308338,RMVar_hsa_circ_287146,RMVar_hsa_circ_87558,RMVar_hsa_circ_107379,RMVar_hsa_circ_180705,RMVar_hsa_circ_180702,RMVar_hsa_circ_180703,RMVar_hsa_circ_319238,RMVar_hsa_circ_368426,RMVar_hsa_circ_84823,RMVar_hsa_circ_180710,RMVar_hsa_circ_289004,RMVar_hsa_circ_180709,RMVar_hsa_circ_36627,RMVar_hsa_circ_180708,RMVar_hsa_circ_291062,RMVar_hsa_circ_75868,RMVar_hsa_circ_283494,RMVar_hsa_circ_180712,RMVar_hsa_circ_180713,RMVar_hsa_circ_180711 22997 RMVar_ID_22997 Human_SNP_ID_614142994 A-to-I Human chr16 - 89754465 89754465 89754465 GGGAGGCTGAGGCAGAAGAATCACTTGAACTCAGGAGGCAGAGGTTGCAGTGAGTTGAGATCATG GGGAGGCTGAGGCAGAAGAATCACTTGAACTCGGGAGGCAGAGGTTGCAGTGAGTTGAGATCATG T C FANCA Ensembl:ENSG00000187741 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1164718396 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_180690,RMVar_hsa_circ_83663,RMVar_hsa_circ_39754,RMVar_hsa_circ_113715,RMVar_hsa_circ_99932,RMVar_hsa_circ_180687,RMVar_hsa_circ_104573,RMVar_hsa_circ_118985,RMVar_hsa_circ_180688,RMVar_hsa_circ_180689,RMVar_hsa_circ_372580,RMVar_hsa_circ_124924,RMVar_hsa_circ_108915,RMVar_hsa_circ_116326,RMVar_hsa_circ_104647,RMVar_hsa_circ_180694,RMVar_hsa_circ_180696,RMVar_hsa_circ_180695,RMVar_hsa_circ_180692,RMVar_hsa_circ_180693,RMVar_hsa_circ_180691,RMVar_hsa_circ_45056,RMVar_hsa_circ_65065,RMVar_hsa_circ_90173,RMVar_hsa_circ_269291,RMVar_hsa_circ_321202,RMVar_hsa_circ_51929,RMVar_hsa_circ_180704,RMVar_hsa_circ_180701,RMVar_hsa_circ_299494,RMVar_hsa_circ_308338,RMVar_hsa_circ_287146,RMVar_hsa_circ_87558,RMVar_hsa_circ_107379,RMVar_hsa_circ_180705,RMVar_hsa_circ_180702,RMVar_hsa_circ_180703,RMVar_hsa_circ_319238,RMVar_hsa_circ_368426,RMVar_hsa_circ_84823,RMVar_hsa_circ_180710,RMVar_hsa_circ_289004,RMVar_hsa_circ_180709,RMVar_hsa_circ_36627,RMVar_hsa_circ_180708,RMVar_hsa_circ_291062,RMVar_hsa_circ_75868,RMVar_hsa_circ_283494,RMVar_hsa_circ_180712,RMVar_hsa_circ_180713,RMVar_hsa_circ_180711 22998 RMVar_ID_22998 Human_SNP_ID_614143050 A-to-I Human chr16 - 89754641 89754641 89754641 TGTCTGGCCAGGCATGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGGTGAAGTGGGCGGA TGTCTGGCCAGGCATGGTGGCTCATGCCTGTAGTCCCAGCACTTTGGGAGGGTGAAGTGGGCGGA T C FANCA Ensembl:ENSG00000187741 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs762146381 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_180690,RMVar_hsa_circ_83663,RMVar_hsa_circ_39754,RMVar_hsa_circ_113715,RMVar_hsa_circ_99932,RMVar_hsa_circ_180687,RMVar_hsa_circ_104573,RMVar_hsa_circ_118985,RMVar_hsa_circ_180688,RMVar_hsa_circ_180689,RMVar_hsa_circ_372580,RMVar_hsa_circ_124924,RMVar_hsa_circ_108915,RMVar_hsa_circ_116326,RMVar_hsa_circ_104647,RMVar_hsa_circ_180694,RMVar_hsa_circ_180696,RMVar_hsa_circ_180695,RMVar_hsa_circ_180692,RMVar_hsa_circ_180693,RMVar_hsa_circ_180691,RMVar_hsa_circ_45056,RMVar_hsa_circ_65065,RMVar_hsa_circ_90173,RMVar_hsa_circ_269291,RMVar_hsa_circ_321202,RMVar_hsa_circ_51929,RMVar_hsa_circ_180704,RMVar_hsa_circ_180701,RMVar_hsa_circ_299494,RMVar_hsa_circ_308338,RMVar_hsa_circ_287146,RMVar_hsa_circ_87558,RMVar_hsa_circ_107379,RMVar_hsa_circ_180705,RMVar_hsa_circ_180702,RMVar_hsa_circ_180703,RMVar_hsa_circ_319238,RMVar_hsa_circ_368426,RMVar_hsa_circ_84823,RMVar_hsa_circ_180710,RMVar_hsa_circ_289004,RMVar_hsa_circ_180709,RMVar_hsa_circ_36627,RMVar_hsa_circ_180708,RMVar_hsa_circ_291062,RMVar_hsa_circ_75868,RMVar_hsa_circ_283494,RMVar_hsa_circ_180712,RMVar_hsa_circ_180713,RMVar_hsa_circ_180711 22999 RMVar_ID_22999 Human_SNP_ID_614143709 A-to-I Human chr16 - 89756525 89756525 89756525 GACCTCCTGGGCTCAAGTGATCCTCCTGCTTCAGCCCCTCAAGTAGCTGGGACCACAGGCACCAC GACCTCCTGGGCTCAAGTGATCCTCCTGCTTCGGCCCCTCAAGTAGCTGGGACCACAGGCACCAC T C FANCA Ensembl:ENSG00000187741 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1309028900 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_180690,RMVar_hsa_circ_83663,RMVar_hsa_circ_39754,RMVar_hsa_circ_113715,RMVar_hsa_circ_99932,RMVar_hsa_circ_180687,RMVar_hsa_circ_104573,RMVar_hsa_circ_118985,RMVar_hsa_circ_180688,RMVar_hsa_circ_180689,RMVar_hsa_circ_372580,RMVar_hsa_circ_124924,RMVar_hsa_circ_108915,RMVar_hsa_circ_116326,RMVar_hsa_circ_104647,RMVar_hsa_circ_180694,RMVar_hsa_circ_180696,RMVar_hsa_circ_180695,RMVar_hsa_circ_180692,RMVar_hsa_circ_180693,RMVar_hsa_circ_180691,RMVar_hsa_circ_45056,RMVar_hsa_circ_65065,RMVar_hsa_circ_90173,RMVar_hsa_circ_269291,RMVar_hsa_circ_321202,RMVar_hsa_circ_51929,RMVar_hsa_circ_180704,RMVar_hsa_circ_180701,RMVar_hsa_circ_299494,RMVar_hsa_circ_308338,RMVar_hsa_circ_287146,RMVar_hsa_circ_87558,RMVar_hsa_circ_107379,RMVar_hsa_circ_180705,RMVar_hsa_circ_180702,RMVar_hsa_circ_180703,RMVar_hsa_circ_319238,RMVar_hsa_circ_368426,RMVar_hsa_circ_84823,RMVar_hsa_circ_180710,RMVar_hsa_circ_289004,RMVar_hsa_circ_180709,RMVar_hsa_circ_36627,RMVar_hsa_circ_180708,RMVar_hsa_circ_291062,RMVar_hsa_circ_75868,RMVar_hsa_circ_283494,RMVar_hsa_circ_180712,RMVar_hsa_circ_180713,RMVar_hsa_circ_180711 23000 RMVar_ID_23000 Human_SNP_ID_614143919 A-to-I Human chr16 - 89757116 89757116 89757116 AAAAAATTAGCCAGGCATGGTAGTGTGTGCCTATGGTCCCAGCTACTCGTGAGGCTGAGGTGGGA AAAAAATTAGCCAGGCATGGTAGTGTGTGCCTGTGGTCCCAGCTACTCGTGAGGCTGAGGTGGGA T C FANCA Ensembl:ENSG00000187741 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1002197488 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_180690,RMVar_hsa_circ_83663,RMVar_hsa_circ_39754,RMVar_hsa_circ_113715,RMVar_hsa_circ_99932,RMVar_hsa_circ_180687,RMVar_hsa_circ_104573,RMVar_hsa_circ_118985,RMVar_hsa_circ_180688,RMVar_hsa_circ_180689,RMVar_hsa_circ_372580,RMVar_hsa_circ_124924,RMVar_hsa_circ_108915,RMVar_hsa_circ_116326,RMVar_hsa_circ_104647,RMVar_hsa_circ_180694,RMVar_hsa_circ_180696,RMVar_hsa_circ_180695,RMVar_hsa_circ_180692,RMVar_hsa_circ_180693,RMVar_hsa_circ_180691,RMVar_hsa_circ_45056,RMVar_hsa_circ_65065,RMVar_hsa_circ_90173,RMVar_hsa_circ_269291,RMVar_hsa_circ_321202,RMVar_hsa_circ_51929,RMVar_hsa_circ_180704,RMVar_hsa_circ_180701,RMVar_hsa_circ_299494,RMVar_hsa_circ_308338,RMVar_hsa_circ_287146,RMVar_hsa_circ_87558,RMVar_hsa_circ_107379,RMVar_hsa_circ_180705,RMVar_hsa_circ_180702,RMVar_hsa_circ_180703,RMVar_hsa_circ_319238,RMVar_hsa_circ_368426,RMVar_hsa_circ_84823,RMVar_hsa_circ_180710,RMVar_hsa_circ_289004,RMVar_hsa_circ_180709,RMVar_hsa_circ_36627,RMVar_hsa_circ_180708,RMVar_hsa_circ_291062,RMVar_hsa_circ_75868,RMVar_hsa_circ_283494,RMVar_hsa_circ_180712,RMVar_hsa_circ_180713,RMVar_hsa_circ_180711 23001 RMVar_ID_23001 Human_SNP_ID_614146537 A-to-I Human chr16 - 89763449 89763449 89763449 CAAGGTGGCTGGGCACAGTGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCTGAGATGTCAGG CAAGGTGGCTGGGCACAGTGGCTCATGCCTATGATCCCAGCACTTTGGGAGGCTGAGATGTCAGG T C FANCA Ensembl:ENSG00000187741 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs990155215 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12859274 RMVar_hsa_circ_180690,RMVar_hsa_circ_83663,RMVar_hsa_circ_39754,RMVar_hsa_circ_99932,RMVar_hsa_circ_104573,RMVar_hsa_circ_118985,RMVar_hsa_circ_180688,RMVar_hsa_circ_180689,RMVar_hsa_circ_372580,RMVar_hsa_circ_124924,RMVar_hsa_circ_108915,RMVar_hsa_circ_104647,RMVar_hsa_circ_180694,RMVar_hsa_circ_180695,RMVar_hsa_circ_180692,RMVar_hsa_circ_180693,RMVar_hsa_circ_180691,RMVar_hsa_circ_29947,RMVar_hsa_circ_45056,RMVar_hsa_circ_269291,RMVar_hsa_circ_321202,RMVar_hsa_circ_287146,RMVar_hsa_circ_87558,RMVar_hsa_circ_107379,RMVar_hsa_circ_180702,RMVar_hsa_circ_180703,RMVar_hsa_circ_84823,RMVar_hsa_circ_93397,RMVar_hsa_circ_289004,RMVar_hsa_circ_180709,RMVar_hsa_circ_36627,RMVar_hsa_circ_75868,RMVar_hsa_circ_180712,RMVar_hsa_circ_180713,RMVar_hsa_circ_370289,RMVar_hsa_circ_370593,RMVar_hsa_circ_335628,RMVar_hsa_circ_284848,RMVar_hsa_circ_95015,RMVar_hsa_circ_114220,RMVar_hsa_circ_93472,RMVar_hsa_circ_84140,RMVar_hsa_circ_86018,RMVar_hsa_circ_76368,RMVar_hsa_circ_89109,RMVar_hsa_circ_180717,RMVar_hsa_circ_180721,RMVar_hsa_circ_180723,RMVar_hsa_circ_180724,RMVar_hsa_circ_180722,RMVar_hsa_circ_180719,RMVar_hsa_circ_180720,RMVar_hsa_circ_180718,RMVar_hsa_circ_122470,RMVar_hsa_circ_180715,RMVar_hsa_circ_180716,RMVar_hsa_circ_180714,RMVar_hsa_circ_318467,RMVar_hsa_circ_115747,RMVar_hsa_circ_119521,RMVar_hsa_circ_112173,RMVar_hsa_circ_180732,RMVar_hsa_circ_37285,RMVar_hsa_circ_57204,RMVar_hsa_circ_180733,RMVar_hsa_circ_180734,RMVar_hsa_circ_180730,RMVar_hsa_circ_180731,RMVar_hsa_circ_180729 23002 RMVar_ID_23002 Human_SNP_ID_614146538 A-to-I Human chr16 - 89763451 89763451 89763451 TTCAAGGTGGCTGGGCACAGTGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCTGAGATGTCA TTCAAGGTGGCTGGGCACAGTGGCTCATGCCTTTAATCCCAGCACTTTGGGAGGCTGAGATGTCA T A FANCA Ensembl:ENSG00000187741 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs915120536 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12859274 RMVar_hsa_circ_180690,RMVar_hsa_circ_83663,RMVar_hsa_circ_39754,RMVar_hsa_circ_99932,RMVar_hsa_circ_104573,RMVar_hsa_circ_118985,RMVar_hsa_circ_180688,RMVar_hsa_circ_180689,RMVar_hsa_circ_372580,RMVar_hsa_circ_124924,RMVar_hsa_circ_108915,RMVar_hsa_circ_104647,RMVar_hsa_circ_180694,RMVar_hsa_circ_180695,RMVar_hsa_circ_180692,RMVar_hsa_circ_180693,RMVar_hsa_circ_180691,RMVar_hsa_circ_29947,RMVar_hsa_circ_45056,RMVar_hsa_circ_269291,RMVar_hsa_circ_321202,RMVar_hsa_circ_287146,RMVar_hsa_circ_87558,RMVar_hsa_circ_107379,RMVar_hsa_circ_180702,RMVar_hsa_circ_180703,RMVar_hsa_circ_84823,RMVar_hsa_circ_93397,RMVar_hsa_circ_289004,RMVar_hsa_circ_180709,RMVar_hsa_circ_36627,RMVar_hsa_circ_75868,RMVar_hsa_circ_180712,RMVar_hsa_circ_180713,RMVar_hsa_circ_370289,RMVar_hsa_circ_370593,RMVar_hsa_circ_335628,RMVar_hsa_circ_284848,RMVar_hsa_circ_95015,RMVar_hsa_circ_114220,RMVar_hsa_circ_93472,RMVar_hsa_circ_84140,RMVar_hsa_circ_86018,RMVar_hsa_circ_76368,RMVar_hsa_circ_89109,RMVar_hsa_circ_180717,RMVar_hsa_circ_180721,RMVar_hsa_circ_180723,RMVar_hsa_circ_180724,RMVar_hsa_circ_180722,RMVar_hsa_circ_180719,RMVar_hsa_circ_180720,RMVar_hsa_circ_180718,RMVar_hsa_circ_122470,RMVar_hsa_circ_180715,RMVar_hsa_circ_180716,RMVar_hsa_circ_180714,RMVar_hsa_circ_318467,RMVar_hsa_circ_115747,RMVar_hsa_circ_119521,RMVar_hsa_circ_112173,RMVar_hsa_circ_180732,RMVar_hsa_circ_37285,RMVar_hsa_circ_57204,RMVar_hsa_circ_180733,RMVar_hsa_circ_180734,RMVar_hsa_circ_180730,RMVar_hsa_circ_180731,RMVar_hsa_circ_180729 23003 RMVar_ID_23003 Human_SNP_ID_614146539 A-to-I Human chr16 - 89763451 89763451 89763451 TTCAAGGTGGCTGGGCACAGTGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCTGAGATGTCA TTCAAGGTGGCTGGGCACAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGATGTCA T C FANCA Ensembl:ENSG00000187741 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs915120536 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12859274 RMVar_hsa_circ_180690,RMVar_hsa_circ_83663,RMVar_hsa_circ_39754,RMVar_hsa_circ_99932,RMVar_hsa_circ_104573,RMVar_hsa_circ_118985,RMVar_hsa_circ_180688,RMVar_hsa_circ_180689,RMVar_hsa_circ_372580,RMVar_hsa_circ_124924,RMVar_hsa_circ_108915,RMVar_hsa_circ_104647,RMVar_hsa_circ_180694,RMVar_hsa_circ_180695,RMVar_hsa_circ_180692,RMVar_hsa_circ_180693,RMVar_hsa_circ_180691,RMVar_hsa_circ_29947,RMVar_hsa_circ_45056,RMVar_hsa_circ_269291,RMVar_hsa_circ_321202,RMVar_hsa_circ_287146,RMVar_hsa_circ_87558,RMVar_hsa_circ_107379,RMVar_hsa_circ_180702,RMVar_hsa_circ_180703,RMVar_hsa_circ_84823,RMVar_hsa_circ_93397,RMVar_hsa_circ_289004,RMVar_hsa_circ_180709,RMVar_hsa_circ_36627,RMVar_hsa_circ_75868,RMVar_hsa_circ_180712,RMVar_hsa_circ_180713,RMVar_hsa_circ_370289,RMVar_hsa_circ_370593,RMVar_hsa_circ_335628,RMVar_hsa_circ_284848,RMVar_hsa_circ_95015,RMVar_hsa_circ_114220,RMVar_hsa_circ_93472,RMVar_hsa_circ_84140,RMVar_hsa_circ_86018,RMVar_hsa_circ_76368,RMVar_hsa_circ_89109,RMVar_hsa_circ_180717,RMVar_hsa_circ_180721,RMVar_hsa_circ_180723,RMVar_hsa_circ_180724,RMVar_hsa_circ_180722,RMVar_hsa_circ_180719,RMVar_hsa_circ_180720,RMVar_hsa_circ_180718,RMVar_hsa_circ_122470,RMVar_hsa_circ_180715,RMVar_hsa_circ_180716,RMVar_hsa_circ_180714,RMVar_hsa_circ_318467,RMVar_hsa_circ_115747,RMVar_hsa_circ_119521,RMVar_hsa_circ_112173,RMVar_hsa_circ_180732,RMVar_hsa_circ_37285,RMVar_hsa_circ_57204,RMVar_hsa_circ_180733,RMVar_hsa_circ_180734,RMVar_hsa_circ_180730,RMVar_hsa_circ_180731,RMVar_hsa_circ_180729 23004 RMVar_ID_23004 Human_SNP_ID_614146546 A-to-I Human chr16 - 89763465 89763465 89763465 CTTTAGAAAAGAATTTCAAGGTGGCTGGGCACAGTGGCTCATGCCTATAATCCCAGCACTTTGGG CTTTAGAAAAGAATTTCAAGGTGGCTGGGCACTGTGGCTCATGCCTATAATCCCAGCACTTTGGG T A FANCA Ensembl:ENSG00000187741 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs897227283 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6547864 RMVar_hsa_circ_180690,RMVar_hsa_circ_83663,RMVar_hsa_circ_39754,RMVar_hsa_circ_99932,RMVar_hsa_circ_104573,RMVar_hsa_circ_118985,RMVar_hsa_circ_180688,RMVar_hsa_circ_180689,RMVar_hsa_circ_372580,RMVar_hsa_circ_124924,RMVar_hsa_circ_108915,RMVar_hsa_circ_104647,RMVar_hsa_circ_180694,RMVar_hsa_circ_180695,RMVar_hsa_circ_180692,RMVar_hsa_circ_180693,RMVar_hsa_circ_180691,RMVar_hsa_circ_29947,RMVar_hsa_circ_45056,RMVar_hsa_circ_269291,RMVar_hsa_circ_321202,RMVar_hsa_circ_287146,RMVar_hsa_circ_87558,RMVar_hsa_circ_107379,RMVar_hsa_circ_180702,RMVar_hsa_circ_180703,RMVar_hsa_circ_84823,RMVar_hsa_circ_93397,RMVar_hsa_circ_289004,RMVar_hsa_circ_180709,RMVar_hsa_circ_36627,RMVar_hsa_circ_75868,RMVar_hsa_circ_180712,RMVar_hsa_circ_180713,RMVar_hsa_circ_370289,RMVar_hsa_circ_370593,RMVar_hsa_circ_335628,RMVar_hsa_circ_284848,RMVar_hsa_circ_95015,RMVar_hsa_circ_114220,RMVar_hsa_circ_93472,RMVar_hsa_circ_84140,RMVar_hsa_circ_86018,RMVar_hsa_circ_76368,RMVar_hsa_circ_89109,RMVar_hsa_circ_180717,RMVar_hsa_circ_180721,RMVar_hsa_circ_180723,RMVar_hsa_circ_180724,RMVar_hsa_circ_180722,RMVar_hsa_circ_180719,RMVar_hsa_circ_180720,RMVar_hsa_circ_180718,RMVar_hsa_circ_122470,RMVar_hsa_circ_180715,RMVar_hsa_circ_180716,RMVar_hsa_circ_180714,RMVar_hsa_circ_318467,RMVar_hsa_circ_115747,RMVar_hsa_circ_119521,RMVar_hsa_circ_112173,RMVar_hsa_circ_180732,RMVar_hsa_circ_37285,RMVar_hsa_circ_57204,RMVar_hsa_circ_180733,RMVar_hsa_circ_180734,RMVar_hsa_circ_180730,RMVar_hsa_circ_180731,RMVar_hsa_circ_180729 23005 RMVar_ID_23005 Human_SNP_ID_614146697 A-to-I Human chr16 - 89763821 89763821 89763821 TCAAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCGCGCACCACCACGCCTG TCAAGTGATTCTCCTGCCTCAGCCTCCCAAGTGGCTGGGACTACAGGCGCGCACCACCACGCCTG T C FANCA Ensembl:ENSG00000187741 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1479405541 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_180690,RMVar_hsa_circ_83663,RMVar_hsa_circ_39754,RMVar_hsa_circ_99932,RMVar_hsa_circ_104573,RMVar_hsa_circ_118985,RMVar_hsa_circ_180688,RMVar_hsa_circ_180689,RMVar_hsa_circ_372580,RMVar_hsa_circ_124924,RMVar_hsa_circ_108915,RMVar_hsa_circ_104647,RMVar_hsa_circ_180694,RMVar_hsa_circ_180695,RMVar_hsa_circ_180692,RMVar_hsa_circ_180693,RMVar_hsa_circ_180691,RMVar_hsa_circ_29947,RMVar_hsa_circ_45056,RMVar_hsa_circ_269291,RMVar_hsa_circ_321202,RMVar_hsa_circ_287146,RMVar_hsa_circ_87558,RMVar_hsa_circ_107379,RMVar_hsa_circ_180702,RMVar_hsa_circ_180703,RMVar_hsa_circ_84823,RMVar_hsa_circ_93397,RMVar_hsa_circ_289004,RMVar_hsa_circ_180709,RMVar_hsa_circ_36627,RMVar_hsa_circ_75868,RMVar_hsa_circ_180712,RMVar_hsa_circ_180713,RMVar_hsa_circ_370289,RMVar_hsa_circ_370593,RMVar_hsa_circ_335628,RMVar_hsa_circ_284848,RMVar_hsa_circ_95015,RMVar_hsa_circ_114220,RMVar_hsa_circ_93472,RMVar_hsa_circ_84140,RMVar_hsa_circ_86018,RMVar_hsa_circ_76368,RMVar_hsa_circ_89109,RMVar_hsa_circ_180717,RMVar_hsa_circ_180721,RMVar_hsa_circ_180723,RMVar_hsa_circ_180724,RMVar_hsa_circ_180722,RMVar_hsa_circ_180719,RMVar_hsa_circ_180720,RMVar_hsa_circ_180718,RMVar_hsa_circ_122470,RMVar_hsa_circ_180715,RMVar_hsa_circ_180716,RMVar_hsa_circ_180714,RMVar_hsa_circ_318467,RMVar_hsa_circ_115747,RMVar_hsa_circ_119521,RMVar_hsa_circ_112173,RMVar_hsa_circ_180732,RMVar_hsa_circ_37285,RMVar_hsa_circ_57204,RMVar_hsa_circ_180733,RMVar_hsa_circ_180734,RMVar_hsa_circ_180730,RMVar_hsa_circ_180731,RMVar_hsa_circ_180729 23006 RMVar_ID_23006 Human_SNP_ID_614146818 A-to-I Human chr16 - 89764059 89764059 89764059 TTTGGTATCTTTAGTACAGACGGGGTTTCACCATGTTGTCCAGGCTGGTCTTAAACTCCTGGCCT TTTGGTATCTTTAGTACAGACGGGGTTTCACCGTGTTGTCCAGGCTGGTCTTAAACTCCTGGCCT T C FANCA Ensembl:ENSG00000187741 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs780034715 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_180690,RMVar_hsa_circ_83663,RMVar_hsa_circ_39754,RMVar_hsa_circ_99932,RMVar_hsa_circ_104573,RMVar_hsa_circ_118985,RMVar_hsa_circ_180688,RMVar_hsa_circ_180689,RMVar_hsa_circ_372580,RMVar_hsa_circ_124924,RMVar_hsa_circ_108915,RMVar_hsa_circ_104647,RMVar_hsa_circ_180694,RMVar_hsa_circ_180695,RMVar_hsa_circ_180692,RMVar_hsa_circ_180693,RMVar_hsa_circ_180691,RMVar_hsa_circ_29947,RMVar_hsa_circ_45056,RMVar_hsa_circ_269291,RMVar_hsa_circ_321202,RMVar_hsa_circ_287146,RMVar_hsa_circ_87558,RMVar_hsa_circ_107379,RMVar_hsa_circ_180702,RMVar_hsa_circ_180703,RMVar_hsa_circ_84823,RMVar_hsa_circ_93397,RMVar_hsa_circ_289004,RMVar_hsa_circ_180709,RMVar_hsa_circ_36627,RMVar_hsa_circ_75868,RMVar_hsa_circ_180712,RMVar_hsa_circ_180713,RMVar_hsa_circ_370289,RMVar_hsa_circ_370593,RMVar_hsa_circ_335628,RMVar_hsa_circ_284848,RMVar_hsa_circ_95015,RMVar_hsa_circ_114220,RMVar_hsa_circ_93472,RMVar_hsa_circ_84140,RMVar_hsa_circ_86018,RMVar_hsa_circ_76368,RMVar_hsa_circ_89109,RMVar_hsa_circ_180717,RMVar_hsa_circ_180721,RMVar_hsa_circ_180723,RMVar_hsa_circ_180724,RMVar_hsa_circ_180722,RMVar_hsa_circ_180719,RMVar_hsa_circ_180720,RMVar_hsa_circ_180718,RMVar_hsa_circ_122470,RMVar_hsa_circ_180715,RMVar_hsa_circ_180716,RMVar_hsa_circ_180714,RMVar_hsa_circ_318467,RMVar_hsa_circ_115747,RMVar_hsa_circ_119521,RMVar_hsa_circ_112173,RMVar_hsa_circ_180732,RMVar_hsa_circ_37285,RMVar_hsa_circ_57204,RMVar_hsa_circ_180733,RMVar_hsa_circ_180734,RMVar_hsa_circ_180730,RMVar_hsa_circ_180731,RMVar_hsa_circ_180729 23007 RMVar_ID_23007 Human_SNP_ID_614148338 A-to-I Human chr16 - 89767505 89767505 89767505 GAATCAGCTGGGCATGGTGGGAGATGCCTGTAATCCCAGCTACCTGGGAGGCTGAGGCAGGAGAC GAATCAGCTGGGCATGGTGGGAGATGCCTGTAGTCCCAGCTACCTGGGAGGCTGAGGCAGGAGAC T C FANCA Ensembl:ENSG00000187741 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1216174304 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22802773 RMVar_hsa_circ_180690,RMVar_hsa_circ_83663,RMVar_hsa_circ_39754,RMVar_hsa_circ_99932,RMVar_hsa_circ_104573,RMVar_hsa_circ_118985,RMVar_hsa_circ_180688,RMVar_hsa_circ_180689,RMVar_hsa_circ_124924,RMVar_hsa_circ_108915,RMVar_hsa_circ_104647,RMVar_hsa_circ_180694,RMVar_hsa_circ_180692,RMVar_hsa_circ_180693,RMVar_hsa_circ_180691,RMVar_hsa_circ_29947,RMVar_hsa_circ_269291,RMVar_hsa_circ_87558,RMVar_hsa_circ_107379,RMVar_hsa_circ_180702,RMVar_hsa_circ_180703,RMVar_hsa_circ_84823,RMVar_hsa_circ_93397,RMVar_hsa_circ_180709,RMVar_hsa_circ_36627,RMVar_hsa_circ_75868,RMVar_hsa_circ_180713,RMVar_hsa_circ_370593,RMVar_hsa_circ_335628,RMVar_hsa_circ_95015,RMVar_hsa_circ_114220,RMVar_hsa_circ_93472,RMVar_hsa_circ_84140,RMVar_hsa_circ_86018,RMVar_hsa_circ_76368,RMVar_hsa_circ_89109,RMVar_hsa_circ_180717,RMVar_hsa_circ_180721,RMVar_hsa_circ_180722,RMVar_hsa_circ_180719,RMVar_hsa_circ_180720,RMVar_hsa_circ_180718,RMVar_hsa_circ_122470,RMVar_hsa_circ_180715,RMVar_hsa_circ_180716,RMVar_hsa_circ_180714,RMVar_hsa_circ_115747,RMVar_hsa_circ_119521,RMVar_hsa_circ_112173,RMVar_hsa_circ_11225,RMVar_hsa_circ_180732,RMVar_hsa_circ_37285,RMVar_hsa_circ_57204,RMVar_hsa_circ_180733,RMVar_hsa_circ_180734,RMVar_hsa_circ_180730,RMVar_hsa_circ_180731,RMVar_hsa_circ_57797,RMVar_hsa_circ_84503,RMVar_hsa_circ_180735,RMVar_hsa_circ_22978 23008 RMVar_ID_23008 Human_SNP_ID_614148339 A-to-I Human chr16 - 89767506 89767506 89767506 AGAATCAGCTGGGCATGGTGGGAGATGCCTGTAATCCCAGCTACCTGGGAGGCTGAGGCAGGAGA AGAATCAGCTGGGCATGGTGGGAGATGCCTGTTATCCCAGCTACCTGGGAGGCTGAGGCAGGAGA T A FANCA Ensembl:ENSG00000187741 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs756408692 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22802773 RMVar_hsa_circ_180690,RMVar_hsa_circ_83663,RMVar_hsa_circ_39754,RMVar_hsa_circ_99932,RMVar_hsa_circ_104573,RMVar_hsa_circ_118985,RMVar_hsa_circ_180688,RMVar_hsa_circ_180689,RMVar_hsa_circ_124924,RMVar_hsa_circ_108915,RMVar_hsa_circ_104647,RMVar_hsa_circ_180694,RMVar_hsa_circ_180692,RMVar_hsa_circ_180693,RMVar_hsa_circ_180691,RMVar_hsa_circ_29947,RMVar_hsa_circ_269291,RMVar_hsa_circ_87558,RMVar_hsa_circ_107379,RMVar_hsa_circ_180702,RMVar_hsa_circ_180703,RMVar_hsa_circ_84823,RMVar_hsa_circ_93397,RMVar_hsa_circ_180709,RMVar_hsa_circ_36627,RMVar_hsa_circ_75868,RMVar_hsa_circ_180713,RMVar_hsa_circ_370593,RMVar_hsa_circ_335628,RMVar_hsa_circ_95015,RMVar_hsa_circ_114220,RMVar_hsa_circ_93472,RMVar_hsa_circ_84140,RMVar_hsa_circ_86018,RMVar_hsa_circ_76368,RMVar_hsa_circ_89109,RMVar_hsa_circ_180717,RMVar_hsa_circ_180721,RMVar_hsa_circ_180722,RMVar_hsa_circ_180719,RMVar_hsa_circ_180720,RMVar_hsa_circ_180718,RMVar_hsa_circ_122470,RMVar_hsa_circ_180715,RMVar_hsa_circ_180716,RMVar_hsa_circ_180714,RMVar_hsa_circ_115747,RMVar_hsa_circ_119521,RMVar_hsa_circ_112173,RMVar_hsa_circ_11225,RMVar_hsa_circ_180732,RMVar_hsa_circ_37285,RMVar_hsa_circ_57204,RMVar_hsa_circ_180733,RMVar_hsa_circ_180734,RMVar_hsa_circ_180730,RMVar_hsa_circ_180731,RMVar_hsa_circ_57797,RMVar_hsa_circ_84503,RMVar_hsa_circ_180735,RMVar_hsa_circ_22978 23009 RMVar_ID_23009 Human_SNP_ID_614148758 A-to-I Human chr16 - 89768637 89768637 89768637 TTGGTTTTTGTTTTGAGACAGAGTCTCACTCTATCGTCCAGGCTGGAGTGCAGTAGCGTGATCTT TTGGTTTTTGTTTTGAGACAGAGTCTCACTCTGTCGTCCAGGCTGGAGTGCAGTAGCGTGATCTT T C FANCA Ensembl:ENSG00000187741 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs184438192 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12859414,Human_RBP_ID_22943921,Human_RBP_ID_23166249,Human_RBP_ID_25238148,Human_RBP_ID_26953251 RMVar_hsa_circ_180690,RMVar_hsa_circ_83663,RMVar_hsa_circ_39754,RMVar_hsa_circ_99932,RMVar_hsa_circ_104573,RMVar_hsa_circ_118985,RMVar_hsa_circ_180688,RMVar_hsa_circ_180689,RMVar_hsa_circ_124924,RMVar_hsa_circ_108915,RMVar_hsa_circ_104647,RMVar_hsa_circ_180694,RMVar_hsa_circ_180692,RMVar_hsa_circ_180693,RMVar_hsa_circ_180691,RMVar_hsa_circ_29947,RMVar_hsa_circ_269291,RMVar_hsa_circ_87558,RMVar_hsa_circ_107379,RMVar_hsa_circ_180702,RMVar_hsa_circ_180703,RMVar_hsa_circ_84823,RMVar_hsa_circ_93397,RMVar_hsa_circ_180709,RMVar_hsa_circ_36627,RMVar_hsa_circ_75868,RMVar_hsa_circ_180713,RMVar_hsa_circ_370593,RMVar_hsa_circ_335628,RMVar_hsa_circ_95015,RMVar_hsa_circ_114220,RMVar_hsa_circ_93472,RMVar_hsa_circ_84140,RMVar_hsa_circ_86018,RMVar_hsa_circ_76368,RMVar_hsa_circ_89109,RMVar_hsa_circ_180717,RMVar_hsa_circ_180721,RMVar_hsa_circ_180722,RMVar_hsa_circ_180719,RMVar_hsa_circ_180720,RMVar_hsa_circ_180718,RMVar_hsa_circ_122470,RMVar_hsa_circ_180715,RMVar_hsa_circ_180716,RMVar_hsa_circ_180714,RMVar_hsa_circ_115747,RMVar_hsa_circ_119521,RMVar_hsa_circ_112173,RMVar_hsa_circ_11225,RMVar_hsa_circ_180732,RMVar_hsa_circ_37285,RMVar_hsa_circ_57204,RMVar_hsa_circ_180733,RMVar_hsa_circ_180734,RMVar_hsa_circ_180730,RMVar_hsa_circ_180731,RMVar_hsa_circ_57797,RMVar_hsa_circ_84503,RMVar_hsa_circ_180735,RMVar_hsa_circ_22978 23010 RMVar_ID_23010 Human_SNP_ID_614157266 A-to-I Human chr16 - 89787172 89787172 89787172 TTCCTGCCTCAACCTCCCAAAGTGTTGGAATTACCGGATTGAGCCACTGCACCCAGCCATTAAGT TTCCTGCCTCAACCTCCCAAAGTGTTGGAATTGCCGGATTGAGCCACTGCACCCAGCCATTAAGT T C FANCA Ensembl:ENSG00000187741 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs760767856 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12860045 RMVar_hsa_circ_180690,RMVar_hsa_circ_104573,RMVar_hsa_circ_118985,RMVar_hsa_circ_124924,RMVar_hsa_circ_104647,RMVar_hsa_circ_180692,RMVar_hsa_circ_180693,RMVar_hsa_circ_180691,RMVar_hsa_circ_29947,RMVar_hsa_circ_269291,RMVar_hsa_circ_107379,RMVar_hsa_circ_180702,RMVar_hsa_circ_36627,RMVar_hsa_circ_335628,RMVar_hsa_circ_114220,RMVar_hsa_circ_180715,RMVar_hsa_circ_180714,RMVar_hsa_circ_115747,RMVar_hsa_circ_119521,RMVar_hsa_circ_112173,RMVar_hsa_circ_180732,RMVar_hsa_circ_37285,RMVar_hsa_circ_57204,RMVar_hsa_circ_180733,RMVar_hsa_circ_180734,RMVar_hsa_circ_57797,RMVar_hsa_circ_84503,RMVar_hsa_circ_180735,RMVar_hsa_circ_110423,RMVar_hsa_circ_80022,RMVar_hsa_circ_89693,RMVar_hsa_circ_180739,RMVar_hsa_circ_180740,RMVar_hsa_circ_93729,RMVar_hsa_circ_100923,RMVar_hsa_circ_180742,RMVar_hsa_circ_180744,RMVar_hsa_circ_180743,RMVar_hsa_circ_104046,RMVar_hsa_circ_3101,RMVar_hsa_circ_95425,RMVar_hsa_circ_102907,RMVar_hsa_circ_180745,RMVar_hsa_circ_106799,RMVar_hsa_circ_180747,RMVar_hsa_circ_128184,RMVar_hsa_circ_180748,RMVar_hsa_circ_111171,RMVar_hsa_circ_94376,RMVar_hsa_circ_180752,RMVar_hsa_circ_180753,RMVar_hsa_circ_180754,RMVar_hsa_circ_180751,RMVar_hsa_circ_268508,RMVar_hsa_circ_45994 23011 RMVar_ID_23011 Human_SNP_ID_614157416 A-to-I Human chr16 - 89787519 89787519 89787519 TATGTTGCCCTGGCTGGTCTTTTTGTTTTTTTAAGATGGAGTTCGCTCTTGTTGCCCAGGCTGGA TATGTTGCCCTGGCTGGTCTTTTTGTTTTTTTTAGATGGAGTTCGCTCTTGTTGCCCAGGCTGGA T A FANCA Ensembl:ENSG00000187741 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs888668484 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6547977,Human_RBP_ID_9840468,Human_RBP_ID_25238480 RMVar_hsa_circ_180690,RMVar_hsa_circ_104573,RMVar_hsa_circ_118985,RMVar_hsa_circ_124924,RMVar_hsa_circ_104647,RMVar_hsa_circ_180692,RMVar_hsa_circ_180693,RMVar_hsa_circ_180691,RMVar_hsa_circ_29947,RMVar_hsa_circ_269291,RMVar_hsa_circ_107379,RMVar_hsa_circ_180702,RMVar_hsa_circ_36627,RMVar_hsa_circ_335628,RMVar_hsa_circ_114220,RMVar_hsa_circ_180715,RMVar_hsa_circ_180714,RMVar_hsa_circ_115747,RMVar_hsa_circ_119521,RMVar_hsa_circ_112173,RMVar_hsa_circ_180732,RMVar_hsa_circ_37285,RMVar_hsa_circ_57204,RMVar_hsa_circ_180733,RMVar_hsa_circ_180734,RMVar_hsa_circ_57797,RMVar_hsa_circ_84503,RMVar_hsa_circ_180735,RMVar_hsa_circ_110423,RMVar_hsa_circ_80022,RMVar_hsa_circ_89693,RMVar_hsa_circ_180739,RMVar_hsa_circ_180740,RMVar_hsa_circ_93729,RMVar_hsa_circ_100923,RMVar_hsa_circ_180742,RMVar_hsa_circ_180744,RMVar_hsa_circ_180743,RMVar_hsa_circ_104046,RMVar_hsa_circ_3101,RMVar_hsa_circ_95425,RMVar_hsa_circ_102907,RMVar_hsa_circ_180745,RMVar_hsa_circ_106799,RMVar_hsa_circ_180747,RMVar_hsa_circ_128184,RMVar_hsa_circ_180748,RMVar_hsa_circ_111171,RMVar_hsa_circ_94376,RMVar_hsa_circ_180752,RMVar_hsa_circ_180753,RMVar_hsa_circ_180754,RMVar_hsa_circ_180751,RMVar_hsa_circ_268508,RMVar_hsa_circ_45994 23012 RMVar_ID_23012 Human_SNP_ID_614157417 A-to-I Human chr16 - 89787519 89787519 89787519 TATGTTGCCCTGGCTGGTCTTTTTGTTTTTTTAAGATGGAGTTCGCTCTTGTTGCCCAGGCTGGA TATGTTGCCCTGGCTGGTCTTTTTGTTTTTTTCAGATGGAGTTCGCTCTTGTTGCCCAGGCTGGA T G FANCA Ensembl:ENSG00000187741 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs888668484 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6547977,Human_RBP_ID_9840468,Human_RBP_ID_25238480 RMVar_hsa_circ_180690,RMVar_hsa_circ_104573,RMVar_hsa_circ_118985,RMVar_hsa_circ_124924,RMVar_hsa_circ_104647,RMVar_hsa_circ_180692,RMVar_hsa_circ_180693,RMVar_hsa_circ_180691,RMVar_hsa_circ_29947,RMVar_hsa_circ_269291,RMVar_hsa_circ_107379,RMVar_hsa_circ_180702,RMVar_hsa_circ_36627,RMVar_hsa_circ_335628,RMVar_hsa_circ_114220,RMVar_hsa_circ_180715,RMVar_hsa_circ_180714,RMVar_hsa_circ_115747,RMVar_hsa_circ_119521,RMVar_hsa_circ_112173,RMVar_hsa_circ_180732,RMVar_hsa_circ_37285,RMVar_hsa_circ_57204,RMVar_hsa_circ_180733,RMVar_hsa_circ_180734,RMVar_hsa_circ_57797,RMVar_hsa_circ_84503,RMVar_hsa_circ_180735,RMVar_hsa_circ_110423,RMVar_hsa_circ_80022,RMVar_hsa_circ_89693,RMVar_hsa_circ_180739,RMVar_hsa_circ_180740,RMVar_hsa_circ_93729,RMVar_hsa_circ_100923,RMVar_hsa_circ_180742,RMVar_hsa_circ_180744,RMVar_hsa_circ_180743,RMVar_hsa_circ_104046,RMVar_hsa_circ_3101,RMVar_hsa_circ_95425,RMVar_hsa_circ_102907,RMVar_hsa_circ_180745,RMVar_hsa_circ_106799,RMVar_hsa_circ_180747,RMVar_hsa_circ_128184,RMVar_hsa_circ_180748,RMVar_hsa_circ_111171,RMVar_hsa_circ_94376,RMVar_hsa_circ_180752,RMVar_hsa_circ_180753,RMVar_hsa_circ_180754,RMVar_hsa_circ_180751,RMVar_hsa_circ_268508,RMVar_hsa_circ_45994 23013 RMVar_ID_23013 Human_SNP_ID_614157627 A-to-I Human chr16 - 89788037 89788037 89788037 AAAACCCTATCTCTACCAAAAATACAAAATTTAGCTGGTATGGTGGCAGGTGCCTGTAATCCCAG AAAACCCTATCTCTACCAAAAATACAAAATTTCGCTGGTATGGTGGCAGGTGCCTGTAATCCCAG T G FANCA Ensembl:ENSG00000187741 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs954088680 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25238495 RMVar_hsa_circ_180690,RMVar_hsa_circ_104573,RMVar_hsa_circ_118985,RMVar_hsa_circ_124924,RMVar_hsa_circ_104647,RMVar_hsa_circ_180692,RMVar_hsa_circ_180693,RMVar_hsa_circ_180691,RMVar_hsa_circ_29947,RMVar_hsa_circ_269291,RMVar_hsa_circ_107379,RMVar_hsa_circ_180702,RMVar_hsa_circ_36627,RMVar_hsa_circ_335628,RMVar_hsa_circ_114220,RMVar_hsa_circ_180715,RMVar_hsa_circ_180714,RMVar_hsa_circ_115747,RMVar_hsa_circ_119521,RMVar_hsa_circ_112173,RMVar_hsa_circ_180732,RMVar_hsa_circ_37285,RMVar_hsa_circ_57204,RMVar_hsa_circ_180733,RMVar_hsa_circ_180734,RMVar_hsa_circ_57797,RMVar_hsa_circ_84503,RMVar_hsa_circ_180735,RMVar_hsa_circ_110423,RMVar_hsa_circ_80022,RMVar_hsa_circ_89693,RMVar_hsa_circ_180739,RMVar_hsa_circ_180740,RMVar_hsa_circ_93729,RMVar_hsa_circ_100923,RMVar_hsa_circ_180742,RMVar_hsa_circ_180744,RMVar_hsa_circ_180743,RMVar_hsa_circ_104046,RMVar_hsa_circ_3101,RMVar_hsa_circ_95425,RMVar_hsa_circ_102907,RMVar_hsa_circ_180745,RMVar_hsa_circ_106799,RMVar_hsa_circ_180747,RMVar_hsa_circ_128184,RMVar_hsa_circ_180748,RMVar_hsa_circ_111171,RMVar_hsa_circ_94376,RMVar_hsa_circ_180752,RMVar_hsa_circ_180753,RMVar_hsa_circ_180754,RMVar_hsa_circ_180751,RMVar_hsa_circ_268508,RMVar_hsa_circ_45994 23014 RMVar_ID_23014 Human_SNP_ID_614157638 A-to-I Human chr16 - 89788076 89788076 89788076 TTGAGCCCAGTAGTTCAAGACCACCCTGGGCAACGTGGCAAAACCCTATCTCTACCAAAAATACA TTGAGCCCAGTAGTTCAAGACCACCCTGGGCACCGTGGCAAAACCCTATCTCTACCAAAAATACA T G FANCA Ensembl:ENSG00000187741 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1381822369 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_180690,RMVar_hsa_circ_104573,RMVar_hsa_circ_118985,RMVar_hsa_circ_124924,RMVar_hsa_circ_104647,RMVar_hsa_circ_180692,RMVar_hsa_circ_180693,RMVar_hsa_circ_180691,RMVar_hsa_circ_29947,RMVar_hsa_circ_269291,RMVar_hsa_circ_107379,RMVar_hsa_circ_180702,RMVar_hsa_circ_36627,RMVar_hsa_circ_335628,RMVar_hsa_circ_114220,RMVar_hsa_circ_180715,RMVar_hsa_circ_180714,RMVar_hsa_circ_115747,RMVar_hsa_circ_119521,RMVar_hsa_circ_112173,RMVar_hsa_circ_180732,RMVar_hsa_circ_37285,RMVar_hsa_circ_57204,RMVar_hsa_circ_180733,RMVar_hsa_circ_180734,RMVar_hsa_circ_57797,RMVar_hsa_circ_84503,RMVar_hsa_circ_180735,RMVar_hsa_circ_110423,RMVar_hsa_circ_80022,RMVar_hsa_circ_89693,RMVar_hsa_circ_180739,RMVar_hsa_circ_180740,RMVar_hsa_circ_93729,RMVar_hsa_circ_100923,RMVar_hsa_circ_180742,RMVar_hsa_circ_180744,RMVar_hsa_circ_180743,RMVar_hsa_circ_104046,RMVar_hsa_circ_3101,RMVar_hsa_circ_95425,RMVar_hsa_circ_102907,RMVar_hsa_circ_180745,RMVar_hsa_circ_106799,RMVar_hsa_circ_180747,RMVar_hsa_circ_128184,RMVar_hsa_circ_180748,RMVar_hsa_circ_111171,RMVar_hsa_circ_94376,RMVar_hsa_circ_180752,RMVar_hsa_circ_180753,RMVar_hsa_circ_180754,RMVar_hsa_circ_180751,RMVar_hsa_circ_268508,RMVar_hsa_circ_45994 23015 RMVar_ID_23015 Human_SNP_ID_614157713 A-to-I Human chr16 - 89788313 89788313 89788313 GGGACTACAGGTGCCTGCCACCACACCTGGCTAATTTTTGTAATTTTGGTAGAGATGGGGTCTCA GGGACTACAGGTGCCTGCCACCACACCTGGCTGATTTTTGTAATTTTGGTAGAGATGGGGTCTCA T C FANCA Ensembl:ENSG00000187741 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1227667671 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_180690,RMVar_hsa_circ_104573,RMVar_hsa_circ_118985,RMVar_hsa_circ_124924,RMVar_hsa_circ_104647,RMVar_hsa_circ_180692,RMVar_hsa_circ_180693,RMVar_hsa_circ_180691,RMVar_hsa_circ_29947,RMVar_hsa_circ_269291,RMVar_hsa_circ_107379,RMVar_hsa_circ_180702,RMVar_hsa_circ_36627,RMVar_hsa_circ_335628,RMVar_hsa_circ_114220,RMVar_hsa_circ_180715,RMVar_hsa_circ_180714,RMVar_hsa_circ_115747,RMVar_hsa_circ_119521,RMVar_hsa_circ_112173,RMVar_hsa_circ_180732,RMVar_hsa_circ_37285,RMVar_hsa_circ_57204,RMVar_hsa_circ_180733,RMVar_hsa_circ_180734,RMVar_hsa_circ_57797,RMVar_hsa_circ_84503,RMVar_hsa_circ_180735,RMVar_hsa_circ_110423,RMVar_hsa_circ_80022,RMVar_hsa_circ_89693,RMVar_hsa_circ_180739,RMVar_hsa_circ_180740,RMVar_hsa_circ_93729,RMVar_hsa_circ_100923,RMVar_hsa_circ_180742,RMVar_hsa_circ_180744,RMVar_hsa_circ_180743,RMVar_hsa_circ_104046,RMVar_hsa_circ_3101,RMVar_hsa_circ_95425,RMVar_hsa_circ_102907,RMVar_hsa_circ_180745,RMVar_hsa_circ_106799,RMVar_hsa_circ_180747,RMVar_hsa_circ_128184,RMVar_hsa_circ_180748,RMVar_hsa_circ_111171,RMVar_hsa_circ_94376,RMVar_hsa_circ_180752,RMVar_hsa_circ_180753,RMVar_hsa_circ_180754,RMVar_hsa_circ_180751,RMVar_hsa_circ_268508,RMVar_hsa_circ_45994 23016 RMVar_ID_23016 Human_SNP_ID_614157739 A-to-I Human chr16 - 89788361 89788361 89788361 CACCTCCTGGGTTCAAGCGATTCTCCTGTTTCAGCCTCCTGAGTAGCTGGGACTACAGGTGCCTG CACCTCCTGGGTTCAAGCGATTCTCCTGTTTCTGCCTCCTGAGTAGCTGGGACTACAGGTGCCTG T A FANCA Ensembl:ENSG00000187741 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1050465734 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_180690,RMVar_hsa_circ_104573,RMVar_hsa_circ_118985,RMVar_hsa_circ_124924,RMVar_hsa_circ_104647,RMVar_hsa_circ_180692,RMVar_hsa_circ_180693,RMVar_hsa_circ_180691,RMVar_hsa_circ_29947,RMVar_hsa_circ_269291,RMVar_hsa_circ_107379,RMVar_hsa_circ_180702,RMVar_hsa_circ_36627,RMVar_hsa_circ_335628,RMVar_hsa_circ_114220,RMVar_hsa_circ_180715,RMVar_hsa_circ_180714,RMVar_hsa_circ_115747,RMVar_hsa_circ_119521,RMVar_hsa_circ_112173,RMVar_hsa_circ_180732,RMVar_hsa_circ_37285,RMVar_hsa_circ_57204,RMVar_hsa_circ_180733,RMVar_hsa_circ_180734,RMVar_hsa_circ_57797,RMVar_hsa_circ_84503,RMVar_hsa_circ_180735,RMVar_hsa_circ_110423,RMVar_hsa_circ_80022,RMVar_hsa_circ_89693,RMVar_hsa_circ_180739,RMVar_hsa_circ_180740,RMVar_hsa_circ_93729,RMVar_hsa_circ_100923,RMVar_hsa_circ_180742,RMVar_hsa_circ_180744,RMVar_hsa_circ_180743,RMVar_hsa_circ_104046,RMVar_hsa_circ_3101,RMVar_hsa_circ_95425,RMVar_hsa_circ_102907,RMVar_hsa_circ_180745,RMVar_hsa_circ_106799,RMVar_hsa_circ_180747,RMVar_hsa_circ_128184,RMVar_hsa_circ_180748,RMVar_hsa_circ_111171,RMVar_hsa_circ_94376,RMVar_hsa_circ_180752,RMVar_hsa_circ_180753,RMVar_hsa_circ_180754,RMVar_hsa_circ_180751,RMVar_hsa_circ_268508,RMVar_hsa_circ_45994 23017 RMVar_ID_23017 Human_SNP_ID_614157809 A-to-I Human chr16 - 89788550 89788550 89788550 TCATGCGATCCCCGCACCTTAACCCCCGAAGTACTGGAATTACAGGCATGAGCCACCATGTCCAG TCATGCGATCCCCGCACCTTAACCCCCGAAGTGCTGGAATTACAGGCATGAGCCACCATGTCCAG T C FANCA Ensembl:ENSG00000187741 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs920734591 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_180690,RMVar_hsa_circ_104573,RMVar_hsa_circ_118985,RMVar_hsa_circ_124924,RMVar_hsa_circ_104647,RMVar_hsa_circ_180692,RMVar_hsa_circ_180693,RMVar_hsa_circ_180691,RMVar_hsa_circ_29947,RMVar_hsa_circ_269291,RMVar_hsa_circ_107379,RMVar_hsa_circ_180702,RMVar_hsa_circ_36627,RMVar_hsa_circ_335628,RMVar_hsa_circ_114220,RMVar_hsa_circ_180715,RMVar_hsa_circ_180714,RMVar_hsa_circ_115747,RMVar_hsa_circ_119521,RMVar_hsa_circ_112173,RMVar_hsa_circ_180732,RMVar_hsa_circ_37285,RMVar_hsa_circ_57204,RMVar_hsa_circ_180733,RMVar_hsa_circ_180734,RMVar_hsa_circ_57797,RMVar_hsa_circ_84503,RMVar_hsa_circ_180735,RMVar_hsa_circ_110423,RMVar_hsa_circ_80022,RMVar_hsa_circ_89693,RMVar_hsa_circ_180739,RMVar_hsa_circ_180740,RMVar_hsa_circ_93729,RMVar_hsa_circ_100923,RMVar_hsa_circ_180742,RMVar_hsa_circ_180744,RMVar_hsa_circ_180743,RMVar_hsa_circ_104046,RMVar_hsa_circ_3101,RMVar_hsa_circ_95425,RMVar_hsa_circ_102907,RMVar_hsa_circ_180745,RMVar_hsa_circ_106799,RMVar_hsa_circ_180747,RMVar_hsa_circ_128184,RMVar_hsa_circ_180748,RMVar_hsa_circ_111171,RMVar_hsa_circ_94376,RMVar_hsa_circ_180752,RMVar_hsa_circ_180753,RMVar_hsa_circ_180754,RMVar_hsa_circ_180751,RMVar_hsa_circ_268508,RMVar_hsa_circ_45994 23018 RMVar_ID_23018 Human_SNP_ID_614158555 A-to-I Human chr16 - 89790331 89790331 89790331 GGAGTGCACTGGTGCGACCTCGGCTCACTGCAACCTCCTCCTCCTGGGTTCAAGCAATTCTCCTG GGAGTGCACTGGTGCGACCTCGGCTCACTGCATCCTCCTCCTCCTGGGTTCAAGCAATTCTCCTG T A FANCA Ensembl:ENSG00000187741 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs561981502 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_180690,RMVar_hsa_circ_104573,RMVar_hsa_circ_118985,RMVar_hsa_circ_124924,RMVar_hsa_circ_104647,RMVar_hsa_circ_180692,RMVar_hsa_circ_180693,RMVar_hsa_circ_180691,RMVar_hsa_circ_29947,RMVar_hsa_circ_269291,RMVar_hsa_circ_107379,RMVar_hsa_circ_180702,RMVar_hsa_circ_36627,RMVar_hsa_circ_335628,RMVar_hsa_circ_114220,RMVar_hsa_circ_180715,RMVar_hsa_circ_180714,RMVar_hsa_circ_115747,RMVar_hsa_circ_119521,RMVar_hsa_circ_112173,RMVar_hsa_circ_180732,RMVar_hsa_circ_37285,RMVar_hsa_circ_57204,RMVar_hsa_circ_180733,RMVar_hsa_circ_180734,RMVar_hsa_circ_57797,RMVar_hsa_circ_84503,RMVar_hsa_circ_180735,RMVar_hsa_circ_110423,RMVar_hsa_circ_80022,RMVar_hsa_circ_89693,RMVar_hsa_circ_180739,RMVar_hsa_circ_180740,RMVar_hsa_circ_93729,RMVar_hsa_circ_100923,RMVar_hsa_circ_180742,RMVar_hsa_circ_180744,RMVar_hsa_circ_180743,RMVar_hsa_circ_104046,RMVar_hsa_circ_3101,RMVar_hsa_circ_95425,RMVar_hsa_circ_102907,RMVar_hsa_circ_180745,RMVar_hsa_circ_106799,RMVar_hsa_circ_180747,RMVar_hsa_circ_128184,RMVar_hsa_circ_180748,RMVar_hsa_circ_111171,RMVar_hsa_circ_94376,RMVar_hsa_circ_180752,RMVar_hsa_circ_180753,RMVar_hsa_circ_180754,RMVar_hsa_circ_180751,RMVar_hsa_circ_268508,RMVar_hsa_circ_45994 23019 RMVar_ID_23019 Human_SNP_ID_614158556 A-to-I Human chr16 - 89790331 89790331 89790331 GGAGTGCACTGGTGCGACCTCGGCTCACTGCAACCTCCTCCTCCTGGGTTCAAGCAATTCTCCTG GGAGTGCACTGGTGCGACCTCGGCTCACTGCAGCCTCCTCCTCCTGGGTTCAAGCAATTCTCCTG T C FANCA Ensembl:ENSG00000187741 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs561981502 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_180690,RMVar_hsa_circ_104573,RMVar_hsa_circ_118985,RMVar_hsa_circ_124924,RMVar_hsa_circ_104647,RMVar_hsa_circ_180692,RMVar_hsa_circ_180693,RMVar_hsa_circ_180691,RMVar_hsa_circ_29947,RMVar_hsa_circ_269291,RMVar_hsa_circ_107379,RMVar_hsa_circ_180702,RMVar_hsa_circ_36627,RMVar_hsa_circ_335628,RMVar_hsa_circ_114220,RMVar_hsa_circ_180715,RMVar_hsa_circ_180714,RMVar_hsa_circ_115747,RMVar_hsa_circ_119521,RMVar_hsa_circ_112173,RMVar_hsa_circ_180732,RMVar_hsa_circ_37285,RMVar_hsa_circ_57204,RMVar_hsa_circ_180733,RMVar_hsa_circ_180734,RMVar_hsa_circ_57797,RMVar_hsa_circ_84503,RMVar_hsa_circ_180735,RMVar_hsa_circ_110423,RMVar_hsa_circ_80022,RMVar_hsa_circ_89693,RMVar_hsa_circ_180739,RMVar_hsa_circ_180740,RMVar_hsa_circ_93729,RMVar_hsa_circ_100923,RMVar_hsa_circ_180742,RMVar_hsa_circ_180744,RMVar_hsa_circ_180743,RMVar_hsa_circ_104046,RMVar_hsa_circ_3101,RMVar_hsa_circ_95425,RMVar_hsa_circ_102907,RMVar_hsa_circ_180745,RMVar_hsa_circ_106799,RMVar_hsa_circ_180747,RMVar_hsa_circ_128184,RMVar_hsa_circ_180748,RMVar_hsa_circ_111171,RMVar_hsa_circ_94376,RMVar_hsa_circ_180752,RMVar_hsa_circ_180753,RMVar_hsa_circ_180754,RMVar_hsa_circ_180751,RMVar_hsa_circ_268508,RMVar_hsa_circ_45994 23020 RMVar_ID_23020 Human_SNP_ID_614158716 A-to-I Human chr16 - 89790672 89790672 89790672 GCAGTGGTACAGAAAGCTCACCTTCTCGGCTCACTGCAAACTCCGCTGCCCCGTTTCAAGCTATT GCAGTGGTACAGAAAGCTCACCTTCTCGGCTCGCTGCAAACTCCGCTGCCCCGTTTCAAGCTATT T C FANCA Ensembl:ENSG00000187741 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1324079386 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6548016,Human_RBP_ID_12860185,Human_RBP_ID_23166321 RMVar_hsa_circ_180690,RMVar_hsa_circ_104573,RMVar_hsa_circ_118985,RMVar_hsa_circ_124924,RMVar_hsa_circ_104647,RMVar_hsa_circ_180692,RMVar_hsa_circ_180693,RMVar_hsa_circ_180691,RMVar_hsa_circ_29947,RMVar_hsa_circ_269291,RMVar_hsa_circ_107379,RMVar_hsa_circ_180702,RMVar_hsa_circ_36627,RMVar_hsa_circ_335628,RMVar_hsa_circ_114220,RMVar_hsa_circ_180715,RMVar_hsa_circ_180714,RMVar_hsa_circ_115747,RMVar_hsa_circ_119521,RMVar_hsa_circ_112173,RMVar_hsa_circ_180732,RMVar_hsa_circ_37285,RMVar_hsa_circ_57204,RMVar_hsa_circ_180733,RMVar_hsa_circ_180734,RMVar_hsa_circ_57797,RMVar_hsa_circ_84503,RMVar_hsa_circ_180735,RMVar_hsa_circ_110423,RMVar_hsa_circ_80022,RMVar_hsa_circ_89693,RMVar_hsa_circ_180739,RMVar_hsa_circ_180740,RMVar_hsa_circ_93729,RMVar_hsa_circ_100923,RMVar_hsa_circ_180742,RMVar_hsa_circ_180744,RMVar_hsa_circ_180743,RMVar_hsa_circ_104046,RMVar_hsa_circ_3101,RMVar_hsa_circ_95425,RMVar_hsa_circ_102907,RMVar_hsa_circ_180745,RMVar_hsa_circ_106799,RMVar_hsa_circ_180747,RMVar_hsa_circ_128184,RMVar_hsa_circ_180748,RMVar_hsa_circ_111171,RMVar_hsa_circ_94376,RMVar_hsa_circ_180752,RMVar_hsa_circ_180753,RMVar_hsa_circ_180754,RMVar_hsa_circ_180751,RMVar_hsa_circ_268508,RMVar_hsa_circ_45994 23021 RMVar_ID_23021 Human_SNP_ID_614160315 A-to-I Human chr16 - 89793987 89793987 89793987 CCAGCATTTTGGGAGGCTGAGACGGGCAGGTCACGAGGTCAGAAGTTCGAGACCAGCCTGGCCAA CCAGCATTTTGGGAGGCTGAGACGGGCAGGTCGCGAGGTCAGAAGTTCGAGACCAGCCTGGCCAA T C FANCA Ensembl:ENSG00000187741 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1306809769 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25238597 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_29947,RMVar_hsa_circ_269291,RMVar_hsa_circ_107379,RMVar_hsa_circ_180702,RMVar_hsa_circ_36627,RMVar_hsa_circ_114220,RMVar_hsa_circ_180714,RMVar_hsa_circ_115747,RMVar_hsa_circ_112173,RMVar_hsa_circ_57204,RMVar_hsa_circ_180733,RMVar_hsa_circ_180734,RMVar_hsa_circ_57797,RMVar_hsa_circ_84503,RMVar_hsa_circ_180735,RMVar_hsa_circ_110423,RMVar_hsa_circ_80022,RMVar_hsa_circ_89693,RMVar_hsa_circ_180739,RMVar_hsa_circ_180740,RMVar_hsa_circ_93729,RMVar_hsa_circ_100923,RMVar_hsa_circ_180742,RMVar_hsa_circ_180744,RMVar_hsa_circ_180743,RMVar_hsa_circ_21024,RMVar_hsa_circ_104046,RMVar_hsa_circ_3101,RMVar_hsa_circ_95425,RMVar_hsa_circ_102907,RMVar_hsa_circ_180745,RMVar_hsa_circ_106799,RMVar_hsa_circ_180747,RMVar_hsa_circ_128184,RMVar_hsa_circ_180748,RMVar_hsa_circ_111171,RMVar_hsa_circ_94376,RMVar_hsa_circ_180752,RMVar_hsa_circ_180753,RMVar_hsa_circ_180754,RMVar_hsa_circ_180751,RMVar_hsa_circ_32122,RMVar_hsa_circ_297136,RMVar_hsa_circ_29735,RMVar_hsa_circ_63611,RMVar_hsa_circ_119312,RMVar_hsa_circ_3215,RMVar_hsa_circ_17354,RMVar_hsa_circ_180757,RMVar_hsa_circ_120709,RMVar_hsa_circ_180761,RMVar_hsa_circ_94371,RMVar_hsa_circ_103412,RMVar_hsa_circ_81209,RMVar_hsa_circ_180762,RMVar_hsa_circ_180759,RMVar_hsa_circ_180760,RMVar_hsa_circ_180758 23022 RMVar_ID_23022 Human_SNP_ID_614160475 A-to-I Human chr16 - 89794406 89794406 89794406 AGCTTGAATTACAGGCGCCTGCCACCATGCCCAGCTACTTTTTGTATTTTGAGTAGAGACAGGGT AGCTTGAATTACAGGCGCCTGCCACCATGCCCGGCTACTTTTTGTATTTTGAGTAGAGACAGGGT T C FANCA Ensembl:ENSG00000187741 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1319713108 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25238599 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_29947,RMVar_hsa_circ_269291,RMVar_hsa_circ_107379,RMVar_hsa_circ_180702,RMVar_hsa_circ_36627,RMVar_hsa_circ_114220,RMVar_hsa_circ_180714,RMVar_hsa_circ_115747,RMVar_hsa_circ_112173,RMVar_hsa_circ_57204,RMVar_hsa_circ_180733,RMVar_hsa_circ_180734,RMVar_hsa_circ_57797,RMVar_hsa_circ_84503,RMVar_hsa_circ_180735,RMVar_hsa_circ_110423,RMVar_hsa_circ_80022,RMVar_hsa_circ_89693,RMVar_hsa_circ_180739,RMVar_hsa_circ_180740,RMVar_hsa_circ_93729,RMVar_hsa_circ_100923,RMVar_hsa_circ_180742,RMVar_hsa_circ_180744,RMVar_hsa_circ_180743,RMVar_hsa_circ_21024,RMVar_hsa_circ_104046,RMVar_hsa_circ_3101,RMVar_hsa_circ_95425,RMVar_hsa_circ_102907,RMVar_hsa_circ_180745,RMVar_hsa_circ_106799,RMVar_hsa_circ_180747,RMVar_hsa_circ_128184,RMVar_hsa_circ_180748,RMVar_hsa_circ_111171,RMVar_hsa_circ_94376,RMVar_hsa_circ_180752,RMVar_hsa_circ_180753,RMVar_hsa_circ_180754,RMVar_hsa_circ_180751,RMVar_hsa_circ_32122,RMVar_hsa_circ_297136,RMVar_hsa_circ_29735,RMVar_hsa_circ_63611,RMVar_hsa_circ_119312,RMVar_hsa_circ_3215,RMVar_hsa_circ_17354,RMVar_hsa_circ_180757,RMVar_hsa_circ_120709,RMVar_hsa_circ_180761,RMVar_hsa_circ_94371,RMVar_hsa_circ_103412,RMVar_hsa_circ_81209,RMVar_hsa_circ_180762,RMVar_hsa_circ_180759,RMVar_hsa_circ_180760,RMVar_hsa_circ_180758 23023 RMVar_ID_23023 Human_SNP_ID_614163311 A-to-I Human chr16 - 89801127 89801127 89801127 GTTGGTCAGGCTGGTCTCGAACTTCTGATCTCATGACCCGCCCACCTTGGCCTCTCAAAGTGTTG GTTGGTCAGGCTGGTCTCGAACTTCTGATCTCGTGACCCGCCCACCTTGGCCTCTCAAAGTGTTG T C FANCA Ensembl:ENSG00000187741 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1224658253 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12860583,Human_RBP_ID_25247589 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_107379,RMVar_hsa_circ_180702,RMVar_hsa_circ_114220,RMVar_hsa_circ_180714,RMVar_hsa_circ_115747,RMVar_hsa_circ_112173,RMVar_hsa_circ_57204,RMVar_hsa_circ_180733,RMVar_hsa_circ_180734,RMVar_hsa_circ_57797,RMVar_hsa_circ_84503,RMVar_hsa_circ_180735,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_111171,RMVar_hsa_circ_180753,RMVar_hsa_circ_180754,RMVar_hsa_circ_32122,RMVar_hsa_circ_29735,RMVar_hsa_circ_63611,RMVar_hsa_circ_119312,RMVar_hsa_circ_3215,RMVar_hsa_circ_17354,RMVar_hsa_circ_94371,RMVar_hsa_circ_103412,RMVar_hsa_circ_180759,RMVar_hsa_circ_180760,RMVar_hsa_circ_180758,RMVar_hsa_circ_118243,RMVar_hsa_circ_32349,RMVar_hsa_circ_314291,RMVar_hsa_circ_372013,RMVar_hsa_circ_180764,RMVar_hsa_circ_180766,RMVar_hsa_circ_60302 23024 RMVar_ID_23024 Human_SNP_ID_614163560 A-to-I Human chr16 - 89801725 89801725 89801725 CACCACCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGGTGAGGTTTCACTCTGTTGGCTAGGA CACCACCATGCCCAGCTAATTTTTGTATTTTTGGTAGAGGTGAGGTTTCACTCTGTTGGCTAGGA T C FANCA Ensembl:ENSG00000187741 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1276382600 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12860614 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_107379,RMVar_hsa_circ_180702,RMVar_hsa_circ_114220,RMVar_hsa_circ_180714,RMVar_hsa_circ_115747,RMVar_hsa_circ_112173,RMVar_hsa_circ_57204,RMVar_hsa_circ_180733,RMVar_hsa_circ_180734,RMVar_hsa_circ_57797,RMVar_hsa_circ_84503,RMVar_hsa_circ_180735,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_111171,RMVar_hsa_circ_180753,RMVar_hsa_circ_180754,RMVar_hsa_circ_32122,RMVar_hsa_circ_29735,RMVar_hsa_circ_63611,RMVar_hsa_circ_119312,RMVar_hsa_circ_3215,RMVar_hsa_circ_17354,RMVar_hsa_circ_94371,RMVar_hsa_circ_103412,RMVar_hsa_circ_180759,RMVar_hsa_circ_180760,RMVar_hsa_circ_180758,RMVar_hsa_circ_118243,RMVar_hsa_circ_32349,RMVar_hsa_circ_314291,RMVar_hsa_circ_372013,RMVar_hsa_circ_180764,RMVar_hsa_circ_180766,RMVar_hsa_circ_60302 23025 RMVar_ID_23025 Human_SNP_ID_614163842 A-to-I Human chr16 - 89802377 89802377 89802377 ATAGCTGAGGTTGGGCTCAATGGCTCATGCCTATAATCCAGCACTTTGGGAGGCTGAGACTGGTG ATAGCTGAGGTTGGGCTCAATGGCTCATGCCTGTAATCCAGCACTTTGGGAGGCTGAGACTGGTG T C FANCA Ensembl:ENSG00000187741 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054637053 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12860651,Human_RBP_ID_17564493,Human_RBP_ID_18288345,Human_RBP_ID_25247598 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_107379,RMVar_hsa_circ_180702,RMVar_hsa_circ_114220,RMVar_hsa_circ_180714,RMVar_hsa_circ_115747,RMVar_hsa_circ_112173,RMVar_hsa_circ_57204,RMVar_hsa_circ_180733,RMVar_hsa_circ_180734,RMVar_hsa_circ_57797,RMVar_hsa_circ_84503,RMVar_hsa_circ_180735,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_111171,RMVar_hsa_circ_180753,RMVar_hsa_circ_180754,RMVar_hsa_circ_32122,RMVar_hsa_circ_29735,RMVar_hsa_circ_63611,RMVar_hsa_circ_119312,RMVar_hsa_circ_3215,RMVar_hsa_circ_17354,RMVar_hsa_circ_94371,RMVar_hsa_circ_103412,RMVar_hsa_circ_180759,RMVar_hsa_circ_180760,RMVar_hsa_circ_180758,RMVar_hsa_circ_118243,RMVar_hsa_circ_32349,RMVar_hsa_circ_314291,RMVar_hsa_circ_372013,RMVar_hsa_circ_180764,RMVar_hsa_circ_180766,RMVar_hsa_circ_60302 23026 RMVar_ID_23026 Human_SNP_ID_614164847 A-to-I Human chr16 - 89804840 89804840 89804840 TTTAGTAGAGACGGGGTTTCATTAGGTTGGCCAGGCTGCTCTTGAACTCCTGACCTCGTGATGCA TTTAGTAGAGACGGGGTTTCATTAGGTTGGCCGGGCTGCTCTTGAACTCCTGACCTCGTGATGCA T C FANCA Ensembl:ENSG00000187741 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs375746372 Functional Loss SNV dbSNP153 33..33 33 - - - 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_180768 23027 RMVar_ID_23027 Human_SNP_ID_614164848 A-to-I Human chr16 - 89804840 89804840 89804840 TTTAGTAGAGACGGGGTTTCATTAGGTTGGCCAGGCTGCTCTTGAACTCCTGACCTCGTGATGCA TTTAGTAGAGACGGGGTTTCATTAGGTTGGCCCGGCTGCTCTTGAACTCCTGACCTCGTGATGCA T G FANCA Ensembl:ENSG00000187741 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs375746372 Functional Loss SNV dbSNP153 33..33 33 - - - 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_180768 23028 RMVar_ID_23028 Human_SNP_ID_614164859 A-to-I Human chr16 - 89804866 89804866 89804866 TGCCCGGCTAATTTTTTTTTTGTATTTTTAGTAGAGACGGGGTTTCATTAGGTTGGCCAGGCTGC TGCCCGGCTAATTTTTTTTTTGTATTTTTAGTGGAGACGGGGTTTCATTAGGTTGGCCAGGCTGC T C FANCA Ensembl:ENSG00000187741 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1195486812 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12860760 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_180768 23029 RMVar_ID_23029 Human_SNP_ID_614164907 A-to-I Human chr16 - 89804973 89804973 89804973 GGAGTACAGTGGCGCGATCTCAGCTCACTGCAACCTCCGCCTCCTGGGTTCAAGTGATTCTCTGC GGAGTACAGTGGCGCGATCTCAGCTCACTGCAGCCTCCGCCTCCTGGGTTCAAGTGATTCTCTGC T C FANCA Ensembl:ENSG00000187741 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs979579638 Functional Loss SNV dbSNP153 33..33 33 - - - 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_180768 23030 RMVar_ID_23030 Human_SNP_ID_614165433 A-to-I Human chr16 - 89806106 89806105 89806106 GAGTTCAAGACCAGCCTGTCCAACGTGGTGAAACCCTGTCTCTACTAAAATTACAAAAATTAGCT GAGTTCAAGACCAGCCTGTCCAACGTGGTGAA_CCCTGTCTCTACTAAAATTACAAAAATTAGCT GT G FANCA Ensembl:ENSG00000187741 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1368477604 Functional Loss DEL dbSNP153 33..33 33 - - - 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_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_372013,RMVar_hsa_circ_180764,RMVar_hsa_circ_11673,RMVar_hsa_circ_295490,RMVar_hsa_circ_180769 23031 RMVar_ID_23031 Human_SNP_ID_614166044 A-to-I Human chr16 - 89807294 89807294 89807294 TGCCACCACACCCGGCTAATTTTTGTATGTTTAGTAGAGATGGGGTTTCACCATGTTGGCTAGGC TGCCACCACACCCGGCTAATTTTTGTATGTTTGGTAGAGATGGGGTTTCACCATGTTGGCTAGGC T C FANCA Ensembl:ENSG00000187741 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs563316989 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_89 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_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_372013,RMVar_hsa_circ_180764,RMVar_hsa_circ_11673,RMVar_hsa_circ_295490,RMVar_hsa_circ_180769 23032 RMVar_ID_23032 Human_SNP_ID_614166072 A-to-I Human chr16 - 89807367 89807367 89807367 TCGCTGCAACCTCCGCTTCCCGGATTCAAGCAATTCTGCCCCTGCCTCCTCAGTAGCTGGGACTA TCGCTGCAACCTCCGCTTCCCGGATTCAAGCAGTTCTGCCCCTGCCTCCTCAGTAGCTGGGACTA T C FANCA Ensembl:ENSG00000187741 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs952897452 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12860822 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_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_372013,RMVar_hsa_circ_180764,RMVar_hsa_circ_11673,RMVar_hsa_circ_295490,RMVar_hsa_circ_180769 23033 RMVar_ID_23033 Human_SNP_ID_614166073 A-to-I Human chr16 - 89807367 89807367 89807367 TCGCTGCAACCTCCGCTTCCCGGATTCAAGCAATTCTGCCCCTGCCTCCTCAGTAGCTGGGACTA TCGCTGCAACCTCCGCTTCCCGGATTCAAGCACTTCTGCCCCTGCCTCCTCAGTAGCTGGGACTA T G FANCA Ensembl:ENSG00000187741 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs952897452 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12860822 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_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_372013,RMVar_hsa_circ_180764,RMVar_hsa_circ_11673,RMVar_hsa_circ_295490,RMVar_hsa_circ_180769 23034 RMVar_ID_23034 Human_SNP_ID_614166323 A-to-I Human chr16 - 89807883 89807883 89807883 CAGCTAATTTTTGTTATGTATTTATTTTTTTTAGGGACAGAGTCTCGTTCTGTCACCCAGGCTGG CAGCTAATTTTTGTTATGTATTTATTTTTTTTGGGGACAGAGTCTCGTTCTGTCACCCAGGCTGG T C FANCA Ensembl:ENSG00000187741 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs946884448 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12860844 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_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_372013,RMVar_hsa_circ_180764,RMVar_hsa_circ_11673,RMVar_hsa_circ_295490,RMVar_hsa_circ_180769 23035 RMVar_ID_23035 Human_SNP_ID_614166984 A-to-I Human chr16 - 89809187 89809187 89809187 GAGTGCGAGTTAGGGGCCGGGCCCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAG GAGTGCGAGTTAGGGGCCGGGCCCAGTGGCTCGCACCTGTAATCCCAGCACTTTGGGAGGCCGAG T C FANCA Ensembl:ENSG00000187741 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs913826648 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22715613 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 23036 RMVar_ID_23036 Human_SNP_ID_614166988 A-to-I Human chr16 - 89809195 89809195 89809195 ACTGTGAAGAGTGCGAGTTAGGGGCCGGGCCCAGTGGCTCACACCTGTAATCCCAGCACTTTGGG ACTGTGAAGAGTGCGAGTTAGGGGCCGGGCCCCGTGGCTCACACCTGTAATCCCAGCACTTTGGG T G FANCA Ensembl:ENSG00000187741 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1399801262 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9843982,Human_RBP_ID_22715613,Human_RBP_ID_22946585,Human_RBP_ID_25238913 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 23037 RMVar_ID_23037 Human_SNP_ID_614167157 A-to-I Human chr16 - 89809605 89809605 89809605 CCTCAGATGATCTGCCCACCTCGGCCTCCCAAAGTGCCGGGATTACAGGTGTGAGTCACCGCGCC CCTCAGATGATCTGCCCACCTCGGCCTCCCAATGTGCCGGGATTACAGGTGTGAGTCACCGCGCC T A FANCA Ensembl:ENSG00000187741 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs980522457 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25238928 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 23038 RMVar_ID_23038 Human_SNP_ID_614167158 A-to-I Human chr16 - 89809605 89809605 89809605 CCTCAGATGATCTGCCCACCTCGGCCTCCCAAAGTGCCGGGATTACAGGTGTGAGTCACCGCGCC CCTCAGATGATCTGCCCACCTCGGCCTCCCAAGGTGCCGGGATTACAGGTGTGAGTCACCGCGCC T C FANCA Ensembl:ENSG00000187741 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs980522457 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25238928 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 23039 RMVar_ID_23039 Human_SNP_ID_614167159 A-to-I Human chr16 - 89809605 89809605 89809605 CCTCAGATGATCTGCCCACCTCGGCCTCCCAAAGTGCCGGGATTACAGGTGTGAGTCACCGCGCC CCTCAGATGATCTGCCCACCTCGGCCTCCCAACGTGCCGGGATTACAGGTGTGAGTCACCGCGCC T G FANCA Ensembl:ENSG00000187741 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs980522457 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25238928 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 23040 RMVar_ID_23040 Human_SNP_ID_614167208 A-to-I Human chr16 - 89809693 89809693 89809693 ATGCGCCACCATGCCTGGCTAATTTTTTTTGTATTTTTAGTAGAGACGGGGTTTCTCCATGTTGG ATGCGCCACCATGCCTGGCTAATTTTTTTTGTGTTTTTAGTAGAGACGGGGTTTCTCCATGTTGG T C FANCA Ensembl:ENSG00000187741 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1356191628 Functional Loss SNV dbSNP153 33..33 33 - - - 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 23041 RMVar_ID_23041 Human_SNP_ID_614168449 A-to-I Human chr16 - 89812291 89812291 89812291 CTCTGTCGCCCAGACTGCAGTGTAGTGGCGTGATCTCGGCTCACTGCAAACTCCGCCTCCTGGGT CTCTGTCGCCCAGACTGCAGTGTAGTGGCGTGTTCTCGGCTCACTGCAAACTCCGCCTCCTGGGT T A FANCA Ensembl:ENSG00000187741 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1295891291 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12861018 RMVar_hsa_circ_180690,RMVar_hsa_circ_124924,RMVar_hsa_circ_57797,RMVar_hsa_circ_100923,RMVar_hsa_circ_180744,RMVar_hsa_circ_128184,RMVar_hsa_circ_180754,RMVar_hsa_circ_3215,RMVar_hsa_circ_103412,RMVar_hsa_circ_180758,RMVar_hsa_circ_377504,RMVar_hsa_circ_325343 23042 RMVar_ID_23042 Human_SNP_ID_614168993 A-to-I Human chr16 - 89813313 89813313 89813313 GTCTTGACCTCCTGGCCTCAAGTGATCCTCCCACCCCAGCATCTTGAGTAGCTGGGACTACAGGT GTCTTGACCTCCTGGCCTCAAGTGATCCTCCCCCCCCAGCATCTTGAGTAGCTGGGACTACAGGT T G FANCA Ensembl:ENSG00000187741 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs527868769 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12861080 RMVar_hsa_circ_180690,RMVar_hsa_circ_124924,RMVar_hsa_circ_57797,RMVar_hsa_circ_100923,RMVar_hsa_circ_180744,RMVar_hsa_circ_128184,RMVar_hsa_circ_180754,RMVar_hsa_circ_3215,RMVar_hsa_circ_103412,RMVar_hsa_circ_180758,RMVar_hsa_circ_377504,RMVar_hsa_circ_325343 23043 RMVar_ID_23043 Human_SNP_ID_614173089 A-to-I Human chr16 + 89822042 89822042 89822042 TCAGACTCCCAACCCCCAACCTCAGGTGATCTACCCGCCTCAACCTCCCCAAGTGCTGGGATTAC TCAGACTCCCAACCCCCAACCTCAGGTGATCTCCCCGCCTCAACCTCCCCAAGTGCTGGGATTAC A C SPIRE2 Ensembl:ENSG00000204991 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006972828 Functional Loss SNV dbSNP153 33..33 33 - - - 23044 RMVar_ID_23044 Human_SNP_ID_614189074 A-to-I Human chr16 - 89865235 89865233 89865235 TTGGGAGGCAGAGGTGGGCAGATCCTGAGGTCAGGGGATCGAGACCATCCTGGCTAACATGGTGA TTGGGAGGCAGAGGTGGGCAGATCCTGAGGTC__GGGATCGAGACCATCCTGGCTAACATGGTGA CCT C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1425031794 Functional Loss DEL dbSNP153 33..34 33 - - - 23045 RMVar_ID_23045 Human_SNP_ID_614189075 A-to-I Human chr16 - 89865235 89865235 89865235 TTGGGAGGCAGAGGTGGGCAGATCCTGAGGTCAGGGGATCGAGACCATCCTGGCTAACATGGTGA TTGGGAGGCAGAGGTGGGCAGATCCTGAGGTCGGGGGATCGAGACCATCCTGGCTAACATGGTGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1377157536 Functional Loss SNV dbSNP153 33..33 33 - - - 23046 RMVar_ID_23046 Human_SNP_ID_614192683 A-to-I Human chr16 + 89874719 89874708 89874719 AACTCTGCCTCTGCGGGCTCTGCGATCCTCCCACCTCAGCCTCCTGAGTATCTAGGACTACAGGT AACTCTGCCTCTGCGGGCTCTG___________CCTCAGCCTCCTGAGTATCTAGGACTACAGGT GCGATCCTCCCA G TCF25 Ensembl:ENSG00000141002 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334647121 Functional Loss DEL dbSNP153 23..33 33 - - - Human_RBP_ID_12861925 Human_Splice_Rec_1754499 RMVar_hsa_circ_116682,RMVar_hsa_circ_123431,RMVar_hsa_circ_180778,RMVar_hsa_circ_180779 23047 RMVar_ID_23047 Human_SNP_ID_614194997 A-to-I Human chr16 + 89880633 89880633 89880633 AAAGTAAATTGGGTGTTGTGGCGTGTGCCTGTAGTCCCAGCTCCTGGGGAGGCTGAGGCAGGAGG AAAGTAAATTGGGTGTTGTGGCGTGTGCCTGTGGTCCCAGCTCCTGGGGAGGCTGAGGCAGGAGG A G TCF25 Ensembl:ENSG00000141002 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs977338476 Functional Loss SNV dbSNP153 33..33 33 - - - 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_180780 23048 RMVar_ID_23048 Human_SNP_ID_614195362 A-to-I Human chr16 + 89881706 89881706 89881706 GGCTCAGATGATCCTCCTGCCTCAGCCTCCCAAAGCGCTGGGATTATAGGCATGAGCCACCACAC GGCTCAGATGATCCTCCTGCCTCAGCCTCCCAGAGCGCTGGGATTATAGGCATGAGCCACCACAC A G TCF25 Ensembl:ENSG00000141002 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031171105 Functional Loss SNV dbSNP153 33..33 33 - - - 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_180780 23049 RMVar_ID_23049 Human_SNP_ID_614197495 A-to-I Human chr16 + 89887173 89887173 89887173 CTCTTGCCTCAGTCTCCCAAAATGCTGGAATTACAGGTGTGAACCACCACGTCTGGTCAAAAAGT CTCTTGCCTCAGTCTCCCAAAATGCTGGAATTGCAGGTGTGAACCACCACGTCTGGTCAAAAAGT A G TCF25 Ensembl:ENSG00000141002 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1056482964 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6548281 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_302840,RMVar_hsa_circ_180780,RMVar_hsa_circ_338617,RMVar_hsa_circ_180787,RMVar_hsa_circ_180784,RMVar_hsa_circ_180785,RMVar_hsa_circ_86300,RMVar_hsa_circ_359033,RMVar_hsa_circ_180788,RMVar_hsa_circ_180786,RMVar_hsa_circ_374859 23050 RMVar_ID_23050 Human_SNP_ID_614197807 A-to-I Human chr16 + 89888046 89888046 89888046 CCAGCACTTTGGGAGGCTGAGGCGGACAGATCACCTGAAGTCAGGAGTTTGAGACCAGCTGGGCA CCAGCACTTTGGGAGGCTGAGGCGGACAGATCTCCTGAAGTCAGGAGTTTGAGACCAGCTGGGCA A T TCF25 Ensembl:ENSG00000141002 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs747190766 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12862142 RMVar_hsa_circ_31571,RMVar_hsa_circ_116682,RMVar_hsa_circ_123431,RMVar_hsa_circ_180778,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_359033,RMVar_hsa_circ_180786,RMVar_hsa_circ_320969,RMVar_hsa_circ_375037,RMVar_hsa_circ_180789,RMVar_hsa_circ_47080,RMVar_hsa_circ_121737,RMVar_hsa_circ_180791,RMVar_hsa_circ_180792,RMVar_hsa_circ_180790 23051 RMVar_ID_23051 Human_SNP_ID_614197953 A-to-I Human chr16 + 89888509 89888509 89888509 TACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAAACCGGAGGCAGAGGTTGCGGTGAGCTGAGAT TACTCAGGAGGCTGAGGCAGGAGAATCGCTTGTAACCGGAGGCAGAGGTTGCGGTGAGCTGAGAT A T TCF25 Ensembl:ENSG00000141002 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1263434469 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6548291,Human_RBP_ID_12862146 RMVar_hsa_circ_31571,RMVar_hsa_circ_116682,RMVar_hsa_circ_123431,RMVar_hsa_circ_180778,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_359033,RMVar_hsa_circ_180786,RMVar_hsa_circ_320969,RMVar_hsa_circ_375037,RMVar_hsa_circ_180789,RMVar_hsa_circ_47080,RMVar_hsa_circ_121737,RMVar_hsa_circ_180791,RMVar_hsa_circ_180792,RMVar_hsa_circ_180790 23052 RMVar_ID_23052 Human_SNP_ID_614198374 A-to-I Human chr16 + 89889575 89889575 89889575 GTCTGAGTTCTTTTTTTTTTTTTTCGAGACAGAATTTTGCTCTTGTTGCCCAGGCTGGAGTGCAA GTCTGAGTTCTTTTTTTTTTTTTTCGAGACAGCATTTTGCTCTTGTTGCCCAGGCTGGAGTGCAA A C TCF25 Ensembl:ENSG00000141002 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1180333836 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_31571,RMVar_hsa_circ_116682,RMVar_hsa_circ_123431,RMVar_hsa_circ_180778,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_359033,RMVar_hsa_circ_180786,RMVar_hsa_circ_320969,RMVar_hsa_circ_375037,RMVar_hsa_circ_180789,RMVar_hsa_circ_47080,RMVar_hsa_circ_121737,RMVar_hsa_circ_180791,RMVar_hsa_circ_180792,RMVar_hsa_circ_180790 23053 RMVar_ID_23053 Human_SNP_ID_614210291 A-to-I Human chr16 + 89916909 89916904 89916909 TGGAGGTTGCAGTGAGCCAAGAATGCACCACTACACTCCAGCCTGCGCGACAGAGTGAAACTGTC TGGAGGTTGCAGTGAGCCAAGAATGCAC_____CACTCCAGCCTGCGCGACAGAGTGAAACTGTC CCACTA C MC1R,AC092143.3 Ensembl:ENSG00000258839,Ensembl:ENSG00000267048 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs925965501 Functional Loss DEL dbSNP153 29..33 33 - - - 23054 RMVar_ID_23054 Human_SNP_ID_614210295 A-to-I Human chr16 + 89916909 89916909 89916909 TGGAGGTTGCAGTGAGCCAAGAATGCACCACTACACTCCAGCCTGCGCGACAGAGTGAAACTGTC TGGAGGTTGCAGTGAGCCAAGAATGCACCACTGCACTCCAGCCTGCGCGACAGAGTGAAACTGTC A G MC1R,AC092143.3 Ensembl:ENSG00000258839,Ensembl:ENSG00000267048 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1312081320 Functional Loss SNV dbSNP153 33..33 33 - - - 23055 RMVar_ID_23055 Human_SNP_ID_614210622 A-to-I Human chr16 + 89917416 89917416 89917416 GCTATTATCCTGACTCAGCTGGGATTACAGGCACCCACCACCACACCTGGCTGATTTTGGTATTT GCTATTATCCTGACTCAGCTGGGATTACAGGCGCCCACCACCACACCTGGCTGATTTTGGTATTT A G MC1R,AC092143.3 Ensembl:ENSG00000258839,Ensembl:ENSG00000267048 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs75827911 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5247582 23056 RMVar_ID_23056 Human_SNP_ID_614210623 A-to-I Human chr16 + 89917416 89917416 89917416 GCTATTATCCTGACTCAGCTGGGATTACAGGCACCCACCACCACACCTGGCTGATTTTGGTATTT GCTATTATCCTGACTCAGCTGGGATTACAGGCTCCCACCACCACACCTGGCTGATTTTGGTATTT A T MC1R,AC092143.3 Ensembl:ENSG00000258839,Ensembl:ENSG00000267048 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs75827911 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5247582 23057 RMVar_ID_23057 Human_SNP_ID_614210636 A-to-I Human chr16 + 89917454 89917454 89917454 CACCACACCTGGCTGATTTTGGTATTTTTAGTAGAGACGGGGTTTCTCCATGTCGGCCAGGCTGG CACCACACCTGGCTGATTTTGGTATTTTTAGTGGAGACGGGGTTTCTCCATGTCGGCCAGGCTGG A G MC1R,AC092143.3 Ensembl:ENSG00000258839,Ensembl:ENSG00000267048 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs969345415 Functional Loss SNV dbSNP153 33..33 33 - - - 23058 RMVar_ID_23058 Human_SNP_ID_614230509 A-to-I Human chr16 - 89972919 89972919 89972919 AGTTTGGAGACGGAGGAGGCGGGGGGGCGGGAAGCTCTGGCCAGGTGCTGTCGGCCTCACTGCGC AGTTTGGAGACGGAGGAGGCGGGGGGGCGGGAGGCTCTGGCCAGGTGCTGTCGGCCTCACTGCGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1273969412 Functional Loss SNV dbSNP153 33..33 33 - - - 23059 RMVar_ID_23059 Human_SNP_ID_614230708 A-to-I Human chr16 + 89973448 89973448 89973448 GTTGTCTAGGCTGATCTCGAACTCATGGGCACAAGCGATTCTCCTTTCTCAACCTCTGGAGTAGC GTTGTCTAGGCTGATCTCGAACTCATGGGCACGAGCGATTCTCCTTTCTCAACCTCTGGAGTAGC A G AFG3L1P Ensembl:ENSG00000223959 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs763744990 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6548456,Human_RBP_ID_8252544,Human_RBP_ID_12863421,Human_RBP_ID_17372024,Human_RBP_ID_19077745 23060 RMVar_ID_23060 Human_SNP_ID_614231876 A-to-I Human chr16 + 89976742 89976742 89976742 CACCTCCATGCCCGGCTAATTTTTGTATTTTTAGTACAGACGGGGTTTCACCATGTTAGCCAGGC CACCTCCATGCCCGGCTAATTTTTGTATTTTTGGTACAGACGGGGTTTCACCATGTTAGCCAGGC A G AFG3L1P Ensembl:ENSG00000223959 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs550900014 Functional Loss SNV dbSNP153 33..33 33 - - - 23061 RMVar_ID_23061 Human_SNP_ID_614232111 A-to-I Human chr16 + 89977432 89977432 89977432 TTTTAGTCTTACAGTCTTGTTTTTGAAGCTGCAATATTTCAAGTTACTAAATAAATTGCCTCAGT TTTTAGTCTTACAGTCTTGTTTTTGAAGCTGCCATATTTCAAGTTACTAAATAAATTGCCTCAGT A C AFG3L1P Ensembl:ENSG00000223959 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4350572 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6548498,Human_RBP_ID_8443574,Human_RBP_ID_9840715,Human_RBP_ID_23166505,Human_RBP_ID_26639466 23062 RMVar_ID_23062 Human_SNP_ID_614232112 A-to-I Human chr16 + 89977432 89977432 89977432 TTTTAGTCTTACAGTCTTGTTTTTGAAGCTGCAATATTTCAAGTTACTAAATAAATTGCCTCAGT TTTTAGTCTTACAGTCTTGTTTTTGAAGCTGCGATATTTCAAGTTACTAAATAAATTGCCTCAGT A G AFG3L1P Ensembl:ENSG00000223959 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4350572 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6548498,Human_RBP_ID_8443574,Human_RBP_ID_9840715,Human_RBP_ID_23166505,Human_RBP_ID_26639466 23063 RMVar_ID_23063 Human_SNP_ID_614232703 A-to-I Human chr16 + 89979340 89979340 89979340 ACTCTGTCACCCAGGCTGGAGTGCAGTGGCACAATCTCGGCTCACTGCAAGCTCTGCCTCCTGGG ACTCTGTCACCCAGGCTGGAGTGCAGTGGCACGATCTCGGCTCACTGCAAGCTCTGCCTCCTGGG A G AFG3L1P Ensembl:ENSG00000223959 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs890053491 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9841690,Human_RBP_ID_17488608 Human_Splice_Rec_1755202 RMVar_hsa_circ_54150,RMVar_hsa_circ_70110,RMVar_hsa_circ_50120,RMVar_hsa_circ_357189,RMVar_hsa_circ_274763,RMVar_hsa_circ_60878,RMVar_hsa_circ_180865,RMVar_hsa_circ_23484,RMVar_hsa_circ_180864 23064 RMVar_ID_23064 Human_SNP_ID_614232727 A-to-I Human chr16 + 89979425 89979425 89979425 CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGCCGCCCGCCACCATGCCCGGGTAATTTTT CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTGCAGCCGCCCGCCACCATGCCCGGGTAATTTTT A G AFG3L1P Ensembl:ENSG00000223959 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1227387981 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17372608 RMVar_hsa_circ_54150,RMVar_hsa_circ_70110,RMVar_hsa_circ_50120,RMVar_hsa_circ_357189,RMVar_hsa_circ_274763,RMVar_hsa_circ_60878,RMVar_hsa_circ_180865,RMVar_hsa_circ_23484,RMVar_hsa_circ_180864 23065 RMVar_ID_23065 Human_SNP_ID_614233343 A-to-I Human chr16 + 89981248 89981248 89981248 CAGGCTGGAGTGCAGTGATACGATCACTGCTTACTGTAGCCTTGACTTCCCAGGCTCAGATGATT CAGGCTGGAGTGCAGTGATACGATCACTGCTTGCTGTAGCCTTGACTTCCCAGGCTCAGATGATT A G AFG3L1P Ensembl:ENSG00000223959 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1485724562 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54150,RMVar_hsa_circ_70110,RMVar_hsa_circ_50120,RMVar_hsa_circ_357189,RMVar_hsa_circ_60878,RMVar_hsa_circ_42202,RMVar_hsa_circ_180865,RMVar_hsa_circ_23484,RMVar_hsa_circ_353793,RMVar_hsa_circ_17179 23066 RMVar_ID_23066 Human_SNP_ID_614234711 A-to-I Human chr16 + 89985011 89985011 89985011 CCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAATAATTAGCCGGACATGGTGGCCT CCTGGCCAACATGGTGAAACCCCATCTCTACTGAAAATACAATAATTAGCCGGACATGGTGGCCT A G AFG3L1P Ensembl:ENSG00000223959 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs888489909 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54150,RMVar_hsa_circ_70110,RMVar_hsa_circ_60878,RMVar_hsa_circ_42202,RMVar_hsa_circ_353793,RMVar_hsa_circ_81285,RMVar_hsa_circ_180866 23067 RMVar_ID_23067 Human_SNP_ID_614234755 A-to-I Human chr16 + 89985155 89985154 89985156 AGATCATCCCACTGCACTTCAGCCCGGGTGACAGAGGGAGACTGTCTCAAAAAAAAAAAAAAAGA AGATCATCCCACTGCACTTCAGCCCGGGTGAC__AGGGAGACTGTCTCAAAAAAAAAAAAAAAGA CAG C AFG3L1P Ensembl:ENSG00000223959 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1204071583 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_8252561,Human_RBP_ID_9841390,Human_RBP_ID_21973761 RMVar_hsa_circ_54150,RMVar_hsa_circ_70110,RMVar_hsa_circ_60878,RMVar_hsa_circ_42202,RMVar_hsa_circ_353793,RMVar_hsa_circ_81285,RMVar_hsa_circ_180866 23068 RMVar_ID_23068 Human_SNP_ID_614235403 A-to-I Human chr16 + 89986386 89986386 89986386 TCGCCCAGGCTGGAGTGCAGTGGCGCAGTCTCAGCTTGCTGTAACCTCCACCTCCTGGCTTCACA TCGCCCAGGCTGGAGTGCAGTGGCGCAGTCTCGGCTTGCTGTAACCTCCACCTCCTGGCTTCACA A G AFG3L1P Ensembl:ENSG00000223959 Pseudogene intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1385105602 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5247323 RMVar_hsa_circ_70110,RMVar_hsa_circ_60878,RMVar_hsa_circ_353793,RMVar_hsa_circ_81285,RMVar_hsa_circ_180866 23069 RMVar_ID_23069 Human_SNP_ID_614235420 A-to-I Human chr16 + 89986418 89986418 89986418 AGCTTGCTGTAACCTCCACCTCCTGGCTTCACACCATTCTCCTGCCTCAGCCTCCCGAGTAGCCG AGCTTGCTGTAACCTCCACCTCCTGGCTTCACCCCATTCTCCTGCCTCAGCCTCCCGAGTAGCCG A C AFG3L1P Ensembl:ENSG00000223959 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs925822115 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17372617,Human_RBP_ID_18513340 RMVar_hsa_circ_70110,RMVar_hsa_circ_60878,RMVar_hsa_circ_353793,RMVar_hsa_circ_81285,RMVar_hsa_circ_180866 23070 RMVar_ID_23070 Human_SNP_ID_614235421 A-to-I Human chr16 + 89986418 89986418 89986418 AGCTTGCTGTAACCTCCACCTCCTGGCTTCACACCATTCTCCTGCCTCAGCCTCCCGAGTAGCCG AGCTTGCTGTAACCTCCACCTCCTGGCTTCACGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCCG A G AFG3L1P Ensembl:ENSG00000223959 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs925822115 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17372617,Human_RBP_ID_18513340 RMVar_hsa_circ_70110,RMVar_hsa_circ_60878,RMVar_hsa_circ_353793,RMVar_hsa_circ_81285,RMVar_hsa_circ_180866 23071 RMVar_ID_23071 Human_SNP_ID_614235438 A-to-I Human chr16 + 89986456 89986456 89986456 CTCCTGCCTCAGCCTCCCGAGTAGCCGGGACTACAGGCGCCCACCACCACGCCCGGCTAATTTTT CTCCTGCCTCAGCCTCCCGAGTAGCCGGGACTGCAGGCGCCCACCACCACGCCCGGCTAATTTTT A G AFG3L1P Ensembl:ENSG00000223959 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs906591351 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17372617 RMVar_hsa_circ_70110,RMVar_hsa_circ_60878,RMVar_hsa_circ_353793,RMVar_hsa_circ_81285,RMVar_hsa_circ_180866 23072 RMVar_ID_23072 Human_SNP_ID_614236260 A-to-I Human chr16 + 89988018 89988018 89988018 TAAAAAGTTAAAAAATTATCTGTTGTGGTGGCATGCATGCCTGTGGTTCTAGCTACTCAGGAGGT TAAAAAGTTAAAAAATTATCTGTTGTGGTGGCTTGCATGCCTGTGGTTCTAGCTACTCAGGAGGT A T AFG3L1P Ensembl:ENSG00000223959 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1440538045 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12863963,Human_RBP_ID_17564505,Human_RBP_ID_18513137 RMVar_hsa_circ_70110,RMVar_hsa_circ_60878,RMVar_hsa_circ_353793,RMVar_hsa_circ_81285,RMVar_hsa_circ_180866 23073 RMVar_ID_23073 Human_SNP_ID_614236333 A-to-I Human chr16 + 89988269 89988269 89988269 TGGAGTGTAGTTGTGTAGTCATGGCTCACTGCAGACTTGAACTCCCAGGCACAAGCAATCCTCTT TGGAGTGTAGTTGTGTAGTCATGGCTCACTGCGGACTTGAACTCCCAGGCACAAGCAATCCTCTT A G AFG3L1P Ensembl:ENSG00000223959 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs930080077 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8252462,Human_RBP_ID_12863966,Human_RBP_ID_17564506,Human_RBP_ID_18513260 RMVar_hsa_circ_70110,RMVar_hsa_circ_60878,RMVar_hsa_circ_353793,RMVar_hsa_circ_81285,RMVar_hsa_circ_180866 23074 RMVar_ID_23074 Human_SNP_ID_614236340 A-to-I Human chr16 + 89988283 89988283 89988283 GTAGTCATGGCTCACTGCAGACTTGAACTCCCAGGCACAAGCAATCCTCTTACCTCAGCCTCCTG GTAGTCATGGCTCACTGCAGACTTGAACTCCCGGGCACAAGCAATCCTCTTACCTCAGCCTCCTG A G AFG3L1P Ensembl:ENSG00000223959 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459383085 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5247328,Human_RBP_ID_8252462,Human_RBP_ID_12863966,Human_RBP_ID_17564506,Human_RBP_ID_18513260 RMVar_hsa_circ_70110,RMVar_hsa_circ_60878,RMVar_hsa_circ_353793,RMVar_hsa_circ_81285,RMVar_hsa_circ_180866 23075 RMVar_ID_23075 Human_SNP_ID_614236343 A-to-I Human chr16 + 89988289 89988289 89988289 ATGGCTCACTGCAGACTTGAACTCCCAGGCACAAGCAATCCTCTTACCTCAGCCTCCTGAGGAGC ATGGCTCACTGCAGACTTGAACTCCCAGGCACGAGCAATCCTCTTACCTCAGCCTCCTGAGGAGC A G AFG3L1P Ensembl:ENSG00000223959 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1323149363 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5247328,Human_RBP_ID_8252462,Human_RBP_ID_12863966,Human_RBP_ID_17564506,Human_RBP_ID_18513260,Human_RBP_ID_23307819 RMVar_hsa_circ_70110,RMVar_hsa_circ_60878,RMVar_hsa_circ_353793,RMVar_hsa_circ_81285,RMVar_hsa_circ_180866 23076 RMVar_ID_23076 Human_SNP_ID_614236374 A-to-I Human chr16 + 89988379 89988379 89988379 GCCCAACTAATTTTTGTATTTTTACTAGAGACAGGGTTTCACCAGGTTGTTTAGGCTGGTCTCGA GCCCAACTAATTTTTGTATTTTTACTAGAGACGGGGTTTCACCAGGTTGTTTAGGCTGGTCTCGA A G AFG3L1P Ensembl:ENSG00000223959 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs374495772 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70110,RMVar_hsa_circ_60878,RMVar_hsa_circ_353793,RMVar_hsa_circ_81285,RMVar_hsa_circ_180866 23077 RMVar_ID_23077 Human_SNP_ID_614236415 A-to-I Human chr16 + 89988534 89988534 89988534 TTTTTTAGAGACGGAGTCTTGCCACGTTGCCCAGGCTGGTCTTGAACTTCTGGGCTCAAGAGATC TTTTTTAGAGACGGAGTCTTGCCACGTTGCCCGGGCTGGTCTTGAACTTCTGGGCTCAAGAGATC A G AFG3L1P Ensembl:ENSG00000223959 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1352071110 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5096562,Human_RBP_ID_5247329,Human_RBP_ID_6548561,Human_RBP_ID_8941664,Human_RBP_ID_12869663 RMVar_hsa_circ_70110,RMVar_hsa_circ_60878,RMVar_hsa_circ_353793,RMVar_hsa_circ_81285,RMVar_hsa_circ_180866 23078 RMVar_ID_23078 Human_SNP_ID_614236421 A-to-I Human chr16 + 89988559 89988558 89988560 GTTGCCCAGGCTGGTCTTGAACTTCTGGGCTCAAGAGATCCTCTCACCGTGGCTTCCCAAAGTGC GTTGCCCAGGCTGGTCTTGAACTTCTGGGCTC__GAGATCCTCTCACCGTGGCTTCCCAAAGTGC CAA C AFG3L1P Ensembl:ENSG00000223959 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1486882728 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_5096562,Human_RBP_ID_8941664,Human_RBP_ID_12863974,Human_RBP_ID_18513176 RMVar_hsa_circ_70110,RMVar_hsa_circ_60878,RMVar_hsa_circ_353793,RMVar_hsa_circ_81285,RMVar_hsa_circ_180866 23079 RMVar_ID_23079 Human_SNP_ID_614238778 A-to-I Human chr16 - 89995333 89995333 89995333 GGGGCAGTGCTGAGTCATCCCTGCTGAGGGGCAGTACTGAGTCATCCCTGCTGAGGGGCAGTACT GGGGCAGTGCTGAGTCATCCCTGCTGAGGGGCGGTACTGAGTCATCCCTGCTGAGGGGCAGTACT T C lnc-DBNDD1-1 RNACentral:URS00008B82A6 lincRNA intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1374615493 Functional Loss SNV dbSNP153 33..33 33 - - - 23080 RMVar_ID_23080 Human_SNP_ID_614239494 A-to-I Human chr16 + 89997227 89997227 89997227 AGGCAGAGGTTGCAGTGAGCCAGGATCGTGCCACTGCACTCCAATCTGGGCGACAGAGCAAGACT AGGCAGAGGTTGCAGTGAGCCAGGATCGTGCCGCTGCACTCCAATCTGGGCGACAGAGCAAGACT A G AFG3L1P Ensembl:ENSG00000223959 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs916928323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18513165 RMVar_hsa_circ_70110,RMVar_hsa_circ_81285,RMVar_hsa_circ_180866 23081 RMVar_ID_23081 Human_SNP_ID_441963483 A-to-I Human chr10 + 90901226 90901226 90901226 TGAGGCTGGTCTCAAACTCCTAGGATCAAGCCATCCTCCCGCTTTGGCCTCCTAAAGTGCTGGGA TGAGGCTGGTCTCAAACTCCTAGGATCAAGCCGTCCTCCCGCTTTGGCCTCCTAAAGTGCTGGGA A G RPP30 Ensembl:ENSG00000148688 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs950298237 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_384804 RMVar_hsa_circ_29045,RMVar_hsa_circ_296010,RMVar_hsa_circ_144837 23082 RMVar_ID_23082 Human_SNP_ID_442177795 A-to-I Human chr10 + 91803255 91803255 91803255 GTAAATGAGGCCCGGGCACAGTGCCACAGGCTATAATCCCAGCACTCTGGGAGGCAAAGGCAGGA GTAAATGAGGCCCGGGCACAGTGCCACAGGCTGTAATCCCAGCACTCTGGGAGGCAAAGGCAGGA A G TNKS2 Ensembl:ENSG00000107854 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1564600171 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_144867,RMVar_hsa_circ_124373 23083 RMVar_ID_23083 Human_SNP_ID_442182869 A-to-I Human chr10 + 91822609 91822609 91822609 TGTTTTTTTGAGACAAGGTCTCACTCTTGCCCAGGCCGGAGTGCAGTGGTGCAATCTTGGCTCAC TGTTTTTTTGAGACAAGGTCTCACTCTTGCCCGGGCCGGAGTGCAGTGGTGCAATCTTGGCTCAC A G TNKS2 Ensembl:ENSG00000107854 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1246178928 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11457664,Human_RBP_ID_22708587 RMVar_hsa_circ_15873,RMVar_hsa_circ_63214,RMVar_hsa_circ_144867,RMVar_hsa_circ_124373,RMVar_hsa_circ_115081,RMVar_hsa_circ_53450,RMVar_hsa_circ_57678,RMVar_hsa_circ_316441,RMVar_hsa_circ_305009,RMVar_hsa_circ_144870,RMVar_hsa_circ_324445,RMVar_hsa_circ_290585,RMVar_hsa_circ_50300,RMVar_hsa_circ_53177,RMVar_hsa_circ_144872,RMVar_hsa_circ_144873,RMVar_hsa_circ_363676,RMVar_hsa_circ_53628,RMVar_hsa_circ_16816,RMVar_hsa_circ_21842,RMVar_hsa_circ_15961,RMVar_hsa_circ_144874,RMVar_hsa_circ_31928 23084 RMVar_ID_23084 Human_SNP_ID_442214248 A-to-I Human chr10 + 91949162 91949162 91949162 GAGAGAAGACCCCACCTCCACAAAAAATAAAAAATTAACTGGGTTTGGTGGTGCATGCCTGTGGT GAGAGAAGACCCCACCTCCACAAAAAATAAAACATTAACTGGGTTTGGTGGTGCATGCCTGTGGT A C BTAF1 Ensembl:ENSG00000095564 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs984707665 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5278,RMVar_hsa_circ_24397,RMVar_hsa_circ_300700,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_144905,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_144913,RMVar_hsa_circ_144914,RMVar_hsa_circ_144915,RMVar_hsa_circ_144912 23085 RMVar_ID_23085 Human_SNP_ID_442214249 A-to-I Human chr10 + 91949166 91949166 91949166 GAAGACCCCACCTCCACAAAAAATAAAAAATTAACTGGGTTTGGTGGTGCATGCCTGTGGTCCCA GAAGACCCCACCTCCACAAAAAATAAAAAATTGACTGGGTTTGGTGGTGCATGCCTGTGGTCCCA A G BTAF1 Ensembl:ENSG00000095564 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1274328345 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5278,RMVar_hsa_circ_24397,RMVar_hsa_circ_300700,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_144905,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_144913,RMVar_hsa_circ_144914,RMVar_hsa_circ_144915,RMVar_hsa_circ_144912 23086 RMVar_ID_23086 Human_SNP_ID_442214811 A-to-I Human chr10 + 91950960 91950960 91950960 GAAGCAAGCCTCTCGCCTTCAGCCCCTGGAGTAGCTGGGACTACAGGTGTGTACCATCATGCCCT GAAGCAAGCCTCTCGCCTTCAGCCCCTGGAGTCGCTGGGACTACAGGTGTGTACCATCATGCCCT A C BTAF1 Ensembl:ENSG00000095564 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs929300500 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11459058 RMVar_hsa_circ_5278,RMVar_hsa_circ_24397,RMVar_hsa_circ_300700,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_144905,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_144913,RMVar_hsa_circ_144914,RMVar_hsa_circ_144915,RMVar_hsa_circ_144912 23087 RMVar_ID_23087 Human_SNP_ID_442214812 A-to-I Human chr10 + 91950960 91950960 91950960 GAAGCAAGCCTCTCGCCTTCAGCCCCTGGAGTAGCTGGGACTACAGGTGTGTACCATCATGCCCT GAAGCAAGCCTCTCGCCTTCAGCCCCTGGAGTGGCTGGGACTACAGGTGTGTACCATCATGCCCT A G BTAF1 Ensembl:ENSG00000095564 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs929300500 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11459058 RMVar_hsa_circ_5278,RMVar_hsa_circ_24397,RMVar_hsa_circ_300700,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_144905,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_144913,RMVar_hsa_circ_144914,RMVar_hsa_circ_144915,RMVar_hsa_circ_144912 23088 RMVar_ID_23088 Human_SNP_ID_442215170 A-to-I Human chr10 + 91952309 91952309 91952309 CTTCATGCTGTTTTGTTTTGTGGCTGTACCATAATTTCACTCTTTTCTTCCTCTTCCTCTATTCC CTTCATGCTGTTTTGTTTTGTGGCTGTACCATTATTTCACTCTTTTCTTCCTCTTCCTCTATTCC A T BTAF1 Ensembl:ENSG00000095564 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1205717207 Functional Loss SNV dbSNP153 33..33 33 - - - 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 23089 RMVar_ID_23089 Human_SNP_ID_442215770 A-to-I Human chr10 + 91954747 91954747 91954747 GTGTGGCTAATTTTTAAATTTTTTGTAGACATAAGGTCTTCCTATGTTGCCTAGGCTGGTCTCTA GTGTGGCTAATTTTTAAATTTTTTGTAGACATGAGGTCTTCCTATGTTGCCTAGGCTGGTCTCTA A G BTAF1 Ensembl:ENSG00000095564 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053325931 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11459164,Human_RBP_ID_18600252 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_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_311052,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_319166,RMVar_hsa_circ_144913,RMVar_hsa_circ_144914,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_64826,RMVar_hsa_circ_91375,RMVar_hsa_circ_73984,RMVar_hsa_circ_34351,RMVar_hsa_circ_144925 23090 RMVar_ID_23090 Human_SNP_ID_442216682 A-to-I Human chr10 + 91958330 91958330 91958330 TGCCCACCTGGGCCTTCCAAAGTGCTGGGATTACAAGTGTGAGCCACCTCGCCCAGCCTGGAGCT TGCCCACCTGGGCCTTCCAAAGTGCTGGGATTTCAAGTGTGAGCCACCTCGCCCAGCCTGGAGCT A T BTAF1 Ensembl:ENSG00000095564 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1319505382 Functional Loss SNV dbSNP153 33..33 33 - - - 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_23172,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_62614,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_74282,RMVar_hsa_circ_48734,RMVar_hsa_circ_144928,RMVar_hsa_circ_144929,RMVar_hsa_circ_144930 23091 RMVar_ID_23091 Human_SNP_ID_442218066 A-to-I Human chr10 + 91963298 91963298 91963298 ATTTTTTAAAAGGCATGGTGGCGGGCGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGTAGGAGA ATTTTTTAAAAGGCATGGTGGCGGGCGCCTGTGGTCCCAGCTACTCAGGAGGCTGAGGTAGGAGA A G BTAF1 Ensembl:ENSG00000095564 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1443323688 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_104454 RMVar_hsa_circ_5278,RMVar_hsa_circ_341436,RMVar_hsa_circ_107889,RMVar_hsa_circ_144903,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_311052,RMVar_hsa_circ_378426,RMVar_hsa_circ_327701,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_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_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_144926,RMVar_hsa_circ_144927,RMVar_hsa_circ_314365,RMVar_hsa_circ_316418,RMVar_hsa_circ_51886,RMVar_hsa_circ_48734,RMVar_hsa_circ_144929,RMVar_hsa_circ_144930,RMVar_hsa_circ_123200,RMVar_hsa_circ_12840,RMVar_hsa_circ_144933,RMVar_hsa_circ_144932,RMVar_hsa_circ_109748,RMVar_hsa_circ_53740,RMVar_hsa_circ_289191,RMVar_hsa_circ_310152,RMVar_hsa_circ_42998,RMVar_hsa_circ_144935,RMVar_hsa_circ_144936,RMVar_hsa_circ_144934 23092 RMVar_ID_23092 Human_SNP_ID_442219603 A-to-I Human chr10 + 91969843 91969843 91969843 AAAATTAGCTGGGCATGATGGTGTCTGCCTGTAATCGTAGCTACTCGGGAGGCTGAGGCACAAGA AAAATTAGCTGGGCATGATGGTGTCTGCCTGTGATCGTAGCTACTCGGGAGGCTGAGGCACAAGA A G BTAF1 Ensembl:ENSG00000095564 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs938384319 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11459555 RMVar_hsa_circ_5278,RMVar_hsa_circ_341436,RMVar_hsa_circ_107889,RMVar_hsa_circ_144903,RMVar_hsa_circ_303323,RMVar_hsa_circ_51384,RMVar_hsa_circ_144911,RMVar_hsa_circ_21919,RMVar_hsa_circ_144910,RMVar_hsa_circ_378426,RMVar_hsa_circ_327701,RMVar_hsa_circ_322173,RMVar_hsa_circ_144912,RMVar_hsa_circ_373691,RMVar_hsa_circ_321100,RMVar_hsa_circ_298362,RMVar_hsa_circ_101688,RMVar_hsa_circ_74088,RMVar_hsa_circ_144921,RMVar_hsa_circ_25348,RMVar_hsa_circ_144923,RMVar_hsa_circ_144924,RMVar_hsa_circ_144922,RMVar_hsa_circ_144920,RMVar_hsa_circ_91375,RMVar_hsa_circ_302054,RMVar_hsa_circ_34351,RMVar_hsa_circ_144925,RMVar_hsa_circ_348646,RMVar_hsa_circ_61368,RMVar_hsa_circ_33699,RMVar_hsa_circ_144926,RMVar_hsa_circ_144927,RMVar_hsa_circ_314365,RMVar_hsa_circ_51886,RMVar_hsa_circ_48734,RMVar_hsa_circ_144930,RMVar_hsa_circ_123200,RMVar_hsa_circ_12840,RMVar_hsa_circ_144933,RMVar_hsa_circ_144932,RMVar_hsa_circ_109748,RMVar_hsa_circ_53740,RMVar_hsa_circ_289191,RMVar_hsa_circ_310152,RMVar_hsa_circ_42998,RMVar_hsa_circ_17234,RMVar_hsa_circ_144935,RMVar_hsa_circ_144936,RMVar_hsa_circ_144934,RMVar_hsa_circ_299189 23093 RMVar_ID_23093 Human_SNP_ID_442228838 A-to-I Human chr10 + 92005951 92005951 92005951 TGGAGGACAGCAGCACAATCACAGCTCACTGCAGCCTCAGCCTCTCCTGGACTCAAGCGATCCTC TGGAGGACAGCAGCACAATCACAGCTCACTGCTGCCTCAGCCTCTCCTGGACTCAAGCGATCCTC A T BTAF1 Ensembl:ENSG00000095564 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1398232023 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107889,RMVar_hsa_circ_144903,RMVar_hsa_circ_21919,RMVar_hsa_circ_4441,RMVar_hsa_circ_373691,RMVar_hsa_circ_101688,RMVar_hsa_circ_74088,RMVar_hsa_circ_144923,RMVar_hsa_circ_144924,RMVar_hsa_circ_91375,RMVar_hsa_circ_144925,RMVar_hsa_circ_61368,RMVar_hsa_circ_33699,RMVar_hsa_circ_314365,RMVar_hsa_circ_48734,RMVar_hsa_circ_144930,RMVar_hsa_circ_123200,RMVar_hsa_circ_144932,RMVar_hsa_circ_289191,RMVar_hsa_circ_42998,RMVar_hsa_circ_144935,RMVar_hsa_circ_144936,RMVar_hsa_circ_299189,RMVar_hsa_circ_308033,RMVar_hsa_circ_35832,RMVar_hsa_circ_346823,RMVar_hsa_circ_287478,RMVar_hsa_circ_316761,RMVar_hsa_circ_355149,RMVar_hsa_circ_364017,RMVar_hsa_circ_348258,RMVar_hsa_circ_127016,RMVar_hsa_circ_112578,RMVar_hsa_circ_144941,RMVar_hsa_circ_362120,RMVar_hsa_circ_144940,RMVar_hsa_circ_299990,RMVar_hsa_circ_276922,RMVar_hsa_circ_279259,RMVar_hsa_circ_272597,RMVar_hsa_circ_144946,RMVar_hsa_circ_144948,RMVar_hsa_circ_144949,RMVar_hsa_circ_144947,RMVar_hsa_circ_144945,RMVar_hsa_circ_280901,RMVar_hsa_circ_287963,RMVar_hsa_circ_362156,RMVar_hsa_circ_369252,RMVar_hsa_circ_309690,RMVar_hsa_circ_57597,RMVar_hsa_circ_144950,RMVar_hsa_circ_144952,RMVar_hsa_circ_144954,RMVar_hsa_circ_144953,RMVar_hsa_circ_144951,RMVar_hsa_circ_144956,RMVar_hsa_circ_127840 23094 RMVar_ID_23094 Human_SNP_ID_442235077 A-to-I Human chr10 + 92030235 92030235 92030235 ATTAAAATTATACTGTTCTGCAGCATTTAGACATTTGTCACATTTCATTAGCTTTGACAACCATA ATTAAAATTATACTGTTCTGCAGCATTTAGACCTTTGTCACATTTCATTAGCTTTGACAACCATA A C BTAF1 Ensembl:ENSG00000095564 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1402723241 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1451695,Human_RBP_ID_1772789,Human_RBP_ID_8341651,Human_RBP_ID_18158968 RMVar_hsa_circ_101688,RMVar_hsa_circ_144924 23095 RMVar_ID_23095 Human_SNP_ID_442268702 A-to-I Human chr10 - 92178469 92178469 92178469 CCTTCTTCCTTTCTGTCAACCTTCATGTAGGAATAATTGAGATCGCTGGGCGTGGTGCCTCACAT CCTTCTTCCTTTCTGTCAACCTTCATGTAGGAGTAATTGAGATCGCTGGGCGTGGTGCCTCACAT T C CPEB3 Ensembl:ENSG00000107864 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1280162087 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_144960,RMVar_hsa_circ_85070,RMVar_hsa_circ_310304,RMVar_hsa_circ_322768,RMVar_hsa_circ_144961,RMVar_hsa_circ_144962,RMVar_hsa_circ_315103,RMVar_hsa_circ_144970,RMVar_hsa_circ_323511,RMVar_hsa_circ_75516,RMVar_hsa_circ_308805,RMVar_hsa_circ_144972,RMVar_hsa_circ_144973,RMVar_hsa_circ_286026,RMVar_hsa_circ_286844,RMVar_hsa_circ_28629,RMVar_hsa_circ_144977,RMVar_hsa_circ_144975,RMVar_hsa_circ_144974,RMVar_hsa_circ_311961,RMVar_hsa_circ_144978 23096 RMVar_ID_23096 Human_SNP_ID_442295065 A-to-I Human chr10 - 92288292 92288292 92288292 CCATGTCTGGCTTAAAAAAATTTTTTTTGTAGAGATGGTGTTTTGCCATGTTGCCCAGGCTGGTT CCATGTCTGGCTTAAAAAAATTTTTTTTGTAGGGATGGTGTTTTGCCATGTTGCCCAGGCTGGTT T C CPEB3 Ensembl:ENSG00000107864 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1001257658 Functional Loss SNV dbSNP153 33..33 33 - - - 23097 RMVar_ID_23097 Human_SNP_ID_442309463 A-to-I Human chr10 + 92345330 92345330 92345330 GCCAGGAGTTGGAGACCAGCCTGGTCAACATGATGAAACCCCATCTCTACCAAAAATACAAAGAA GCCAGGAGTTGGAGACCAGCCTGGTCAACATGGTGAAACCCCATCTCTACCAAAAATACAAAGAA A G MARCHF5 Ensembl:ENSG00000198060 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs541755049 Functional Loss SNV dbSNP153 33..33 33 - - - 23098 RMVar_ID_23098 Human_SNP_ID_442309588 A-to-I Human chr10 + 92345794 92345794 92345794 CGGCTCACTGCATCCTCGAACTCCCTGGGCTCAGGTGATCCTCCCACCTCAGCCTCCTGCACAGC CGGCTCACTGCATCCTCGAACTCCCTGGGCTCGGGTGATCCTCCCACCTCAGCCTCCTGCACAGC A G MARCHF5 Ensembl:ENSG00000198060 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1489572772 Functional Loss SNV dbSNP153 33..33 33 - - - 23099 RMVar_ID_23099 Human_SNP_ID_442310302 A-to-I Human chr10 + 92348077 92348077 92348077 TGGAGGTGCACACCTGTAATCCCAGCTACTCGAAAGGCTGAGGCAGGAGAATTGCTTGAACCTGG TGGAGGTGCACACCTGTAATCCCAGCTACTCGGAAGGCTGAGGCAGGAGAATTGCTTGAACCTGG A G MARCHF5 Ensembl:ENSG00000198060 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1402927483 Functional Loss SNV dbSNP153 33..33 33 - - - 23100 RMVar_ID_23100 Human_SNP_ID_442310307 A-to-I Human chr10 + 92348115 92348115 92348115 TGAGGCAGGAGAATTGCTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCCAAGATCGTGCCATTGC TGAGGCAGGAGAATTGCTTGAACCTGGGAGGCGGAGGTTGCAGTGAGCCAAGATCGTGCCATTGC A G MARCHF5 Ensembl:ENSG00000198060 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1408996537 Functional Loss SNV dbSNP153 33..33 33 - - - 23101 RMVar_ID_23101 Human_SNP_ID_442336775 A-to-I Human chr10 - 92451482 92451482 92451482 TTGAGACAGAGTCTCGCTCTGTCAGCCAGGCTACAGTGCAGTCGTGCGATCTTGGCTCACTGCAA TTGAGACAGAGTCTCGCTCTGTCAGCCAGGCTCCAGTGCAGTCGTGCGATCTTGGCTCACTGCAA T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1199213135 Functional Loss SNV dbSNP153 33..33 33 - - - 23102 RMVar_ID_23102 Human_SNP_ID_442345659 A-to-I Human chr10 - 92489490 92489490 92489490 TGGAATCTCGCTGTGTCACCATGCTGGAGTACAGTGGCATAATCTTGGCTCACTGCAACCTCCAC TGGAATCTCGCTGTGTCACCATGCTGGAGTACGGTGGCATAATCTTGGCTCACTGCAACCTCCAC T C IDE Ensembl:ENSG00000119912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs957789929 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1758,RMVar_hsa_circ_368837,RMVar_hsa_circ_267056,RMVar_hsa_circ_69308,RMVar_hsa_circ_81572,RMVar_hsa_circ_85165,RMVar_hsa_circ_5412,RMVar_hsa_circ_144985,RMVar_hsa_circ_144986,RMVar_hsa_circ_53793,RMVar_hsa_circ_297135,RMVar_hsa_circ_58995,RMVar_hsa_circ_32093,RMVar_hsa_circ_56428,RMVar_hsa_circ_332929,RMVar_hsa_circ_75617,RMVar_hsa_circ_144988,RMVar_hsa_circ_357720,RMVar_hsa_circ_282810,RMVar_hsa_circ_349808,RMVar_hsa_circ_144990,RMVar_hsa_circ_144991,RMVar_hsa_circ_144992,RMVar_hsa_circ_368335,RMVar_hsa_circ_335834,RMVar_hsa_circ_144994,RMVar_hsa_circ_144996,RMVar_hsa_circ_144995,RMVar_hsa_circ_15703,RMVar_hsa_circ_8295,RMVar_hsa_circ_15446,RMVar_hsa_circ_59708,RMVar_hsa_circ_283158,RMVar_hsa_circ_316998,RMVar_hsa_circ_319331,RMVar_hsa_circ_302913,RMVar_hsa_circ_27727,RMVar_hsa_circ_144997,RMVar_hsa_circ_144999,RMVar_hsa_circ_145000,RMVar_hsa_circ_144998,RMVar_hsa_circ_320854,RMVar_hsa_circ_377362,RMVar_hsa_circ_310493 23103 RMVar_ID_23103 Human_SNP_ID_442358900 A-to-I Human chr10 - 92542233 92542233 92542233 GGAGGATCACCTGAGCCCGGGATGTTGAGGCTATAGTGAACCAAGATTGTGCCTGGGTGACAGAG GGAGGATCACCTGAGCCCGGGATGTTGAGGCTGTAGTGAACCAAGATTGTGCCTGGGTGACAGAG T C IDE Ensembl:ENSG00000119912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232485727 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24845174 RMVar_hsa_circ_1758,RMVar_hsa_circ_69308,RMVar_hsa_circ_332929,RMVar_hsa_circ_144991,RMVar_hsa_circ_59708,RMVar_hsa_circ_27727,RMVar_hsa_circ_366563,RMVar_hsa_circ_315749,RMVar_hsa_circ_145004,RMVar_hsa_circ_359379,RMVar_hsa_circ_145005,RMVar_hsa_circ_11879,RMVar_hsa_circ_22128,RMVar_hsa_circ_35366,RMVar_hsa_circ_328879 23104 RMVar_ID_23104 Human_SNP_ID_442360201 A-to-I Human chr10 - 92548197 92548197 92548197 TGACACCACGCCTGGCTAATTTTGGTGTTTTTAGTAGAGATGGAGTTTCTCGACGTTGGTCAGGC TGACACCACGCCTGGCTAATTTTGGTGTTTTTTGTAGAGATGGAGTTTCTCGACGTTGGTCAGGC T A IDE Ensembl:ENSG00000119912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs375446633 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11462456 RMVar_hsa_circ_1758,RMVar_hsa_circ_69308,RMVar_hsa_circ_332929,RMVar_hsa_circ_144991,RMVar_hsa_circ_59708,RMVar_hsa_circ_27727,RMVar_hsa_circ_366563,RMVar_hsa_circ_315749,RMVar_hsa_circ_145004,RMVar_hsa_circ_359379,RMVar_hsa_circ_145005,RMVar_hsa_circ_11879,RMVar_hsa_circ_22128,RMVar_hsa_circ_35366,RMVar_hsa_circ_328879 23105 RMVar_ID_23105 Human_SNP_ID_442360202 A-to-I Human chr10 - 92548197 92548197 92548197 TGACACCACGCCTGGCTAATTTTGGTGTTTTTAGTAGAGATGGAGTTTCTCGACGTTGGTCAGGC TGACACCACGCCTGGCTAATTTTGGTGTTTTTGGTAGAGATGGAGTTTCTCGACGTTGGTCAGGC T C IDE Ensembl:ENSG00000119912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs375446633 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11462456 RMVar_hsa_circ_1758,RMVar_hsa_circ_69308,RMVar_hsa_circ_332929,RMVar_hsa_circ_144991,RMVar_hsa_circ_59708,RMVar_hsa_circ_27727,RMVar_hsa_circ_366563,RMVar_hsa_circ_315749,RMVar_hsa_circ_145004,RMVar_hsa_circ_359379,RMVar_hsa_circ_145005,RMVar_hsa_circ_11879,RMVar_hsa_circ_22128,RMVar_hsa_circ_35366,RMVar_hsa_circ_328879 23106 RMVar_ID_23106 Human_SNP_ID_442362680 A-to-I Human chr10 - 92557660 92557660 92557660 GTCTCGAACTCCTGGCATCAAGTGATCTGCCTACCTTGGCCTCCCAAAGTGCTGGGATTACAACA GTCTCGAACTCCTGGCATCAAGTGATCTGCCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAACA T C IDE Ensembl:ENSG00000119912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1157530308 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1758,RMVar_hsa_circ_69308,RMVar_hsa_circ_332929,RMVar_hsa_circ_144991,RMVar_hsa_circ_59708,RMVar_hsa_circ_27727,RMVar_hsa_circ_366563,RMVar_hsa_circ_315749,RMVar_hsa_circ_145004,RMVar_hsa_circ_359379,RMVar_hsa_circ_145005,RMVar_hsa_circ_11879,RMVar_hsa_circ_22128,RMVar_hsa_circ_35366,RMVar_hsa_circ_328879 23107 RMVar_ID_23107 Human_SNP_ID_442362692 A-to-I Human chr10 - 92557693 92557693 92557693 TAGAAATGGTGTTTCACCATCTTCGCCAGGCTAGTCTCGAACTCCTGGCATCAAGTGATCTGCCT TAGAAATGGTGTTTCACCATCTTCGCCAGGCTTGTCTCGAACTCCTGGCATCAAGTGATCTGCCT T A IDE Ensembl:ENSG00000119912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1426396706 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1758,RMVar_hsa_circ_69308,RMVar_hsa_circ_332929,RMVar_hsa_circ_144991,RMVar_hsa_circ_59708,RMVar_hsa_circ_27727,RMVar_hsa_circ_366563,RMVar_hsa_circ_315749,RMVar_hsa_circ_145004,RMVar_hsa_circ_359379,RMVar_hsa_circ_145005,RMVar_hsa_circ_11879,RMVar_hsa_circ_22128,RMVar_hsa_circ_35366,RMVar_hsa_circ_328879 23108 RMVar_ID_23108 Human_SNP_ID_442362713 A-to-I Human chr10 - 92557814 92557814 92557814 TTGTAGTGCAGTGACTGCAACCTCCGCCTCCCAGGTTTAAACAATTCTTATGCCTCAGCCTCCTG TTGTAGTGCAGTGACTGCAACCTCCGCCTCCCGGGTTTAAACAATTCTTATGCCTCAGCCTCCTG T C IDE Ensembl:ENSG00000119912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs541633033 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1758,RMVar_hsa_circ_69308,RMVar_hsa_circ_332929,RMVar_hsa_circ_144991,RMVar_hsa_circ_59708,RMVar_hsa_circ_27727,RMVar_hsa_circ_366563,RMVar_hsa_circ_315749,RMVar_hsa_circ_145004,RMVar_hsa_circ_359379,RMVar_hsa_circ_145005,RMVar_hsa_circ_11879,RMVar_hsa_circ_22128,RMVar_hsa_circ_35366,RMVar_hsa_circ_328879 23109 RMVar_ID_23109 Human_SNP_ID_442362884 A-to-I Human chr10 - 92558349 92558349 92558349 TAAGTTTTCTTTTAAGATTTGTATTATTGGCCAGGCATGGTGGCTCACACCTGTAATCCTAGCAC TAAGTTTTCTTTTAAGATTTGTATTATTGGCCGGGCATGGTGGCTCACACCTGTAATCCTAGCAC T C IDE Ensembl:ENSG00000119912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1039508647 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1758,RMVar_hsa_circ_69308,RMVar_hsa_circ_332929,RMVar_hsa_circ_144991,RMVar_hsa_circ_59708,RMVar_hsa_circ_27727,RMVar_hsa_circ_366563,RMVar_hsa_circ_315749,RMVar_hsa_circ_145004,RMVar_hsa_circ_359379,RMVar_hsa_circ_145005,RMVar_hsa_circ_11879,RMVar_hsa_circ_22128,RMVar_hsa_circ_35366,RMVar_hsa_circ_328879 23110 RMVar_ID_23110 Human_SNP_ID_442362987 A-to-I Human chr10 - 92558795 92558795 92558795 CAGTCAGGAGTTCAGGACCAGCCTGACCAACAAGGTGAAACCCCATCTCTACTAATAATACAAAA CAGTCAGGAGTTCAGGACCAGCCTGACCAACAGGGTGAAACCCCATCTCTACTAATAATACAAAA T C IDE Ensembl:ENSG00000119912 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1208490508 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1160163 RMVar_hsa_circ_1758,RMVar_hsa_circ_69308,RMVar_hsa_circ_332929,RMVar_hsa_circ_144991,RMVar_hsa_circ_59708,RMVar_hsa_circ_27727,RMVar_hsa_circ_366563,RMVar_hsa_circ_315749,RMVar_hsa_circ_145004,RMVar_hsa_circ_359379,RMVar_hsa_circ_145005,RMVar_hsa_circ_11879,RMVar_hsa_circ_22128,RMVar_hsa_circ_35366,RMVar_hsa_circ_328879 23111 RMVar_ID_23111 Human_SNP_ID_442373485 A-to-I Human chr10 + 92599414 92599414 92599414 ATGCATCGTGGCGCGTGCCTGTAGTCCCAGCTACTTAGGAGGCTGAGGCAGGAGAATCGCTTGAA ATGCATCGTGGCGCGTGCCTGTAGTCCCAGCTGCTTAGGAGGCTGAGGCAGGAGAATCGCTTGAA A G KIF11 Ensembl:ENSG00000138160 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270256282 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_145011,RMVar_hsa_circ_113828 23112 RMVar_ID_23112 Human_SNP_ID_442377587 A-to-I Human chr10 + 92614837 92614837 92614837 GTAGAGTCTCATACTGTTGCCAAGGCCGCAGTACAGTAGCATGATCATGGCTCACTGCAACTTAA GTAGAGTCTCATACTGTTGCCAAGGCCGCAGTGCAGTAGCATGATCATGGCTCACTGCAACTTAA A G KIF11 Ensembl:ENSG00000138160 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs927087079 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_343337,RMVar_hsa_circ_67654,RMVar_hsa_circ_292400,RMVar_hsa_circ_74661,RMVar_hsa_circ_145013,RMVar_hsa_circ_80720,RMVar_hsa_circ_107961,RMVar_hsa_circ_145015,RMVar_hsa_circ_44390,RMVar_hsa_circ_145016,RMVar_hsa_circ_112251,RMVar_hsa_circ_44440,RMVar_hsa_circ_95838,RMVar_hsa_circ_145017,RMVar_hsa_circ_145018 23113 RMVar_ID_23113 Human_SNP_ID_442377588 A-to-I Human chr10 + 92614837 92614837 92614837 GTAGAGTCTCATACTGTTGCCAAGGCCGCAGTACAGTAGCATGATCATGGCTCACTGCAACTTAA GTAGAGTCTCATACTGTTGCCAAGGCCGCAGTTCAGTAGCATGATCATGGCTCACTGCAACTTAA A T KIF11 Ensembl:ENSG00000138160 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs927087079 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_343337,RMVar_hsa_circ_67654,RMVar_hsa_circ_292400,RMVar_hsa_circ_74661,RMVar_hsa_circ_145013,RMVar_hsa_circ_80720,RMVar_hsa_circ_107961,RMVar_hsa_circ_145015,RMVar_hsa_circ_44390,RMVar_hsa_circ_145016,RMVar_hsa_circ_112251,RMVar_hsa_circ_44440,RMVar_hsa_circ_95838,RMVar_hsa_circ_145017,RMVar_hsa_circ_145018 23114 RMVar_ID_23114 Human_SNP_ID_442377608 A-to-I Human chr10 + 92614920 92614920 92614920 TTCCCCCAACCACAGCCTCCTCCTGAGTAGCTAGTACTACAAGTGTGAGCCACCAGGCCTGGCTA TTCCCCCAACCACAGCCTCCTCCTGAGTAGCTGGTACTACAAGTGTGAGCCACCAGGCCTGGCTA A G KIF11 Ensembl:ENSG00000138160 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs759255560 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_343337,RMVar_hsa_circ_67654,RMVar_hsa_circ_292400,RMVar_hsa_circ_74661,RMVar_hsa_circ_145013,RMVar_hsa_circ_80720,RMVar_hsa_circ_107961,RMVar_hsa_circ_145015,RMVar_hsa_circ_44390,RMVar_hsa_circ_145016,RMVar_hsa_circ_112251,RMVar_hsa_circ_44440,RMVar_hsa_circ_95838,RMVar_hsa_circ_145017,RMVar_hsa_circ_145018 23115 RMVar_ID_23115 Human_SNP_ID_442381890 A-to-I Human chr10 + 92632261 92632261 92632261 CAATCTCTGGCTCACTGCAACCTCCACCTCCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCTTG CAATCTCTGGCTCACTGCAACCTCCACCTCCCCGGTTCAAGCAATTCTCCTGCCTCAGCCTCTTG A C KIF11 Ensembl:ENSG00000138160 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs987522618 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80720,RMVar_hsa_circ_107961,RMVar_hsa_circ_145015,RMVar_hsa_circ_145016,RMVar_hsa_circ_112251,RMVar_hsa_circ_79935,RMVar_hsa_circ_95838,RMVar_hsa_circ_145017,RMVar_hsa_circ_145018,RMVar_hsa_circ_50938,RMVar_hsa_circ_345773,RMVar_hsa_circ_348727,RMVar_hsa_circ_57231,RMVar_hsa_circ_353072,RMVar_hsa_circ_72956,RMVar_hsa_circ_366616,RMVar_hsa_circ_90358,RMVar_hsa_circ_5233,RMVar_hsa_circ_29337,RMVar_hsa_circ_145021,RMVar_hsa_circ_145020 23116 RMVar_ID_23116 Human_SNP_ID_442383000 A-to-I Human chr10 + 92636912 92636912 92636912 AAAATTAGCTGGGTGTGGTGGCTCACACCTATAATCCCAGCTACTCCGGAGGCTGAGGCAGGAGA AAAATTAGCTGGGTGTGGTGGCTCACACCTATGATCCCAGCTACTCCGGAGGCTGAGGCAGGAGA A G KIF11 Ensembl:ENSG00000138160 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1314589659 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80720,RMVar_hsa_circ_107961,RMVar_hsa_circ_145015,RMVar_hsa_circ_145016,RMVar_hsa_circ_112251,RMVar_hsa_circ_79935,RMVar_hsa_circ_95838,RMVar_hsa_circ_145017,RMVar_hsa_circ_145018,RMVar_hsa_circ_50938,RMVar_hsa_circ_345773,RMVar_hsa_circ_57231,RMVar_hsa_circ_353072,RMVar_hsa_circ_366616,RMVar_hsa_circ_90358,RMVar_hsa_circ_100544,RMVar_hsa_circ_5233,RMVar_hsa_circ_145021,RMVar_hsa_circ_145020,RMVar_hsa_circ_357503,RMVar_hsa_circ_10246,RMVar_hsa_circ_145023 23117 RMVar_ID_23117 Human_SNP_ID_442464897 A-to-I Human chr10 + 92978299 92978299 92978299 GGGCATGGTGGCGTGTACCTTTAGTCTTGGCTACTCAGGATGCTGAGGTAGGAGGATGGCTTGAG GGGCATGGTGGCGTGTACCTTTAGTCTTGGCTGCTCAGGATGCTGAGGTAGGAGGATGGCTTGAG A G EXOC6 Ensembl:ENSG00000138190 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs996587662 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3511,RMVar_hsa_circ_145038,RMVar_hsa_circ_317307,RMVar_hsa_circ_287752,RMVar_hsa_circ_378639,RMVar_hsa_circ_343809,RMVar_hsa_circ_336361,RMVar_hsa_circ_145062,RMVar_hsa_circ_351697,RMVar_hsa_circ_145071,RMVar_hsa_circ_11587,RMVar_hsa_circ_353626,RMVar_hsa_circ_145077,RMVar_hsa_circ_50160,RMVar_hsa_circ_358086,RMVar_hsa_circ_298145,RMVar_hsa_circ_315310,RMVar_hsa_circ_296968 23118 RMVar_ID_23118 Human_SNP_ID_442472377 A-to-I Human chr10 + 93011495 93011495 93011495 GTTGCCCAGGCTGGTCTTAAACTCCTGGCTTCAAGCAATCCTCCAGCCTTGGCTTCCCAAAATAC GTTGCCCAGGCTGGTCTTAAACTCCTGGCTTCGAGCAATCCTCCAGCCTTGGCTTCCCAAAATAC A G EXOC6 Ensembl:ENSG00000138190 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs578218741 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_145038,RMVar_hsa_circ_287752,RMVar_hsa_circ_378639,RMVar_hsa_circ_343809,RMVar_hsa_circ_351697,RMVar_hsa_circ_145071,RMVar_hsa_circ_353626,RMVar_hsa_circ_145077,RMVar_hsa_circ_298145,RMVar_hsa_circ_267500,RMVar_hsa_circ_293980,RMVar_hsa_circ_91714,RMVar_hsa_circ_145079,RMVar_hsa_circ_145080,RMVar_hsa_circ_145078 23119 RMVar_ID_23119 Human_SNP_ID_442472381 A-to-I Human chr10 + 93011521 93011520 93011521 GGCTTCAAGCAATCCTCCAGCCTTGGCTTCCCAAAATACTAGGATTTATAGGCATGAGCCACCAT GGCTTCAAGCAATCCTCCAGCCTTGGCTTCCC_AAATACTAGGATTTATAGGCATGAGCCACCAT CA C EXOC6 Ensembl:ENSG00000138190 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1019486050 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_145038,RMVar_hsa_circ_287752,RMVar_hsa_circ_378639,RMVar_hsa_circ_343809,RMVar_hsa_circ_351697,RMVar_hsa_circ_145071,RMVar_hsa_circ_353626,RMVar_hsa_circ_145077,RMVar_hsa_circ_298145,RMVar_hsa_circ_267500,RMVar_hsa_circ_293980,RMVar_hsa_circ_91714,RMVar_hsa_circ_145079,RMVar_hsa_circ_145080,RMVar_hsa_circ_145078 23120 RMVar_ID_23120 Human_SNP_ID_442472382 A-to-I Human chr10 + 93011521 93011521 93011521 GGCTTCAAGCAATCCTCCAGCCTTGGCTTCCCAAAATACTAGGATTTATAGGCATGAGCCACCAT GGCTTCAAGCAATCCTCCAGCCTTGGCTTCCCGAAATACTAGGATTTATAGGCATGAGCCACCAT A G EXOC6 Ensembl:ENSG00000138190 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1447791530 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_145038,RMVar_hsa_circ_287752,RMVar_hsa_circ_378639,RMVar_hsa_circ_343809,RMVar_hsa_circ_351697,RMVar_hsa_circ_145071,RMVar_hsa_circ_353626,RMVar_hsa_circ_145077,RMVar_hsa_circ_298145,RMVar_hsa_circ_267500,RMVar_hsa_circ_293980,RMVar_hsa_circ_91714,RMVar_hsa_circ_145079,RMVar_hsa_circ_145080,RMVar_hsa_circ_145078 23121 RMVar_ID_23121 Human_SNP_ID_442472383 A-to-I Human chr10 + 93011526 93011526 93011526 CAAGCAATCCTCCAGCCTTGGCTTCCCAAAATACTAGGATTTATAGGCATGAGCCACCATGCCCA CAAGCAATCCTCCAGCCTTGGCTTCCCAAAATGCTAGGATTTATAGGCATGAGCCACCATGCCCA A G EXOC6 Ensembl:ENSG00000138190 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs115497254 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2243,GWAS_ID_2244,GWAS_ID_2245,GWAS_ID_2246,GWAS_ID_2247 RMVar_hsa_circ_145038,RMVar_hsa_circ_287752,RMVar_hsa_circ_378639,RMVar_hsa_circ_343809,RMVar_hsa_circ_351697,RMVar_hsa_circ_145071,RMVar_hsa_circ_353626,RMVar_hsa_circ_145077,RMVar_hsa_circ_298145,RMVar_hsa_circ_267500,RMVar_hsa_circ_293980,RMVar_hsa_circ_91714,RMVar_hsa_circ_145079,RMVar_hsa_circ_145080,RMVar_hsa_circ_145078 23122 RMVar_ID_23122 Human_SNP_ID_442569087 A-to-I Human chr10 - 93404075 93404075 93404075 CCAATCATTTCTTCACTACTCTTCTTTCTTCCAGGTTTATAATTCTCACTCTCTGCGGGCAGATT CCAATCATTTCTTCACTACTCTTCTTTCTTCCGGGTTTATAATTCTCACTCTCTGCGGGCAGATT T C MYOF Ensembl:ENSG00000138119 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1564689869 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27217,Human_RBP_ID_2245625,Human_RBP_ID_24846404 Human_Splice_Rec_1160685,Human_Splice_Rec_1160791,Human_Splice_Rec_1160905 RMVar_hsa_circ_88542,RMVar_hsa_circ_106860,RMVar_hsa_circ_89315,RMVar_hsa_circ_145082,RMVar_hsa_circ_145085,RMVar_hsa_circ_12466,RMVar_hsa_circ_145088,RMVar_hsa_circ_100823,RMVar_hsa_circ_145094,RMVar_hsa_circ_27829,RMVar_hsa_circ_116801,RMVar_hsa_circ_145109,RMVar_hsa_circ_23601,RMVar_hsa_circ_38383,RMVar_hsa_circ_11621 23123 RMVar_ID_23123 Human_SNP_ID_442786085 A-to-I Human chr10 + 94319018 94319018 94319018 TGCAGTGAGCCAAGATTACACCACTGTGTTCCAGCCTGGGTGACAGAGCAAGACTTCATCTTTAA TGCAGTGAGCCAAGATTACACCACTGTGTTCCTGCCTGGGTGACAGAGCAAGACTTCATCTTTAA A T PLCE1 Ensembl:ENSG00000138193 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1199068535 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49382,RMVar_hsa_circ_145135,RMVar_hsa_circ_118513,RMVar_hsa_circ_145141,RMVar_hsa_circ_68886,RMVar_hsa_circ_16235,RMVar_hsa_circ_67303 23124 RMVar_ID_23124 Human_SNP_ID_442789015 A-to-I Human chr10 - 94330646 94330646 94330646 ACTCTTGTACCCAGGCTGGAGTGCAGTGGCACAGTCTCCACTCACTGCAACCTCTGCGTCTTGAG ACTCTTGTACCCAGGCTGGAGTGCAGTGGCACCGTCTCCACTCACTGCAACCTCTGCGTCTTGAG T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1465956639 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4132788 23125 RMVar_ID_23125 Human_SNP_ID_442789370 A-to-I Human chr10 - 94332064 94332064 94332064 GAGTTCGAGACCAGCCTTACCAACATAGTGAAACCCCCGTCTCTACTGAAAATAAAAAAAATTAG GAGTTCGAGACCAGCCTTACCAACATAGTGAACCCCCCGTCTCTACTGAAAATAAAAAAAATTAG T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270390187 Functional Loss SNV dbSNP153 33..33 33 - - - 23126 RMVar_ID_23126 Human_SNP_ID_442789371 A-to-I Human chr10 - 94332070 94332070 94332070 GGTCAGGAGTTCGAGACCAGCCTTACCAACATAGTGAAACCCCCGTCTCTACTGAAAATAAAAAA GGTCAGGAGTTCGAGACCAGCCTTACCAACATGGTGAAACCCCCGTCTCTACTGAAAATAAAAAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1338289535 Functional Loss SNV dbSNP153 33..33 33 - - - 23127 RMVar_ID_23127 Human_SNP_ID_442793796 A-to-I Human chr10 - 94349319 94349319 94349319 AAGAAACTCTTTAAGCAAGATAAATTAGGCCAAGCTTCTCTTGGTGTAATTAAAGTGATTTCTGG AAGAAACTCTTTAAGCAAGATAAATTAGGCCAGGCTTCTCTTGGTGTAATTAAAGTGATTTCTGG T C NOC3L Ensembl:ENSG00000173145 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs367917820 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_985047,Human_RBP_ID_1773341,Human_RBP_ID_8764282,Human_RBP_ID_18432185,Human_RBP_ID_23477853,Human_RBP_ID_27612648 Human_Splice_Rec_1161692,Human_Splice_Rec_1161693,Human_Splice_Rec_1161730,Human_Splice_Rec_1161731 RMVar_hsa_circ_115062,RMVar_hsa_circ_122244,RMVar_hsa_circ_145150,RMVar_hsa_circ_78388,RMVar_hsa_circ_145151,RMVar_hsa_circ_145149,RMVar_hsa_circ_64327,RMVar_hsa_circ_145152,RMVar_hsa_circ_64543,RMVar_hsa_circ_12190,RMVar_hsa_circ_41898,RMVar_hsa_circ_107575,RMVar_hsa_circ_110558,RMVar_hsa_circ_343540,RMVar_hsa_circ_63271,RMVar_hsa_circ_145153,RMVar_hsa_circ_145154,RMVar_hsa_circ_76919,RMVar_hsa_circ_145155 23128 RMVar_ID_23128 Human_SNP_ID_442830905 A-to-I Human chr10 + 94501175 94501175 94501175 TTAGCTGCATAAAGAAAAAACTTTAGCCGGGCATGGTGGCTCATGCGTGTAATCCCAGCACTTTG TTAGCTGCATAAAGAAAAAACTTTAGCCGGGCCTGGTGGCTCATGCGTGTAATCCCAGCACTTTG A C TBC1D12 Ensembl:ENSG00000108239 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1313183246 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1283,RMVar_hsa_circ_145167,RMVar_hsa_circ_290782,RMVar_hsa_circ_294926,RMVar_hsa_circ_329268,RMVar_hsa_circ_283336,RMVar_hsa_circ_145168,RMVar_hsa_circ_145163,RMVar_hsa_circ_145165,RMVar_hsa_circ_145166,RMVar_hsa_circ_145164,RMVar_hsa_circ_145162,RMVar_hsa_circ_145181,RMVar_hsa_circ_316167,RMVar_hsa_circ_322501,RMVar_hsa_circ_295649,RMVar_hsa_circ_145179,RMVar_hsa_circ_145180,RMVar_hsa_circ_339997,RMVar_hsa_circ_285903,RMVar_hsa_circ_333606,RMVar_hsa_circ_145197,RMVar_hsa_circ_145189,RMVar_hsa_circ_145190,RMVar_hsa_circ_295537,RMVar_hsa_circ_145187,RMVar_hsa_circ_145188,RMVar_hsa_circ_316644,RMVar_hsa_circ_145186,RMVar_hsa_circ_295980,RMVar_hsa_circ_272113,RMVar_hsa_circ_290634,RMVar_hsa_circ_145198,RMVar_hsa_circ_145200,RMVar_hsa_circ_306391,RMVar_hsa_circ_145195,RMVar_hsa_circ_145196,RMVar_hsa_circ_329132,RMVar_hsa_circ_145202,RMVar_hsa_circ_291241,RMVar_hsa_circ_145201,RMVar_hsa_circ_145199 23129 RMVar_ID_23129 Human_SNP_ID_442831877 A-to-I Human chr10 + 94505473 94505472 94505473 GTGTTGGTGCATGCCAGTAATCCCAGCTACTCAGAAGGCTGAGAATTGCTTGAACCCGGGAGGGG GTGTTGGTGCATGCCAGTAATCCCAGCTACTC_GAAGGCTGAGAATTGCTTGAACCCGGGAGGGG CA C TBC1D12,HELLS Ensembl:ENSG00000108239,Ensembl:ENSG00000119969 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459468372 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_1160423 RMVar_hsa_circ_1283,RMVar_hsa_circ_145167,RMVar_hsa_circ_290782,RMVar_hsa_circ_294926,RMVar_hsa_circ_329268,RMVar_hsa_circ_283336,RMVar_hsa_circ_145168,RMVar_hsa_circ_145163,RMVar_hsa_circ_145165,RMVar_hsa_circ_145166,RMVar_hsa_circ_145164,RMVar_hsa_circ_145162,RMVar_hsa_circ_145181,RMVar_hsa_circ_316167,RMVar_hsa_circ_322501,RMVar_hsa_circ_295649,RMVar_hsa_circ_145179,RMVar_hsa_circ_145180,RMVar_hsa_circ_339997,RMVar_hsa_circ_285903,RMVar_hsa_circ_333606,RMVar_hsa_circ_145197,RMVar_hsa_circ_145189,RMVar_hsa_circ_145190,RMVar_hsa_circ_295537,RMVar_hsa_circ_145187,RMVar_hsa_circ_145188,RMVar_hsa_circ_316644,RMVar_hsa_circ_145186,RMVar_hsa_circ_295980,RMVar_hsa_circ_272113,RMVar_hsa_circ_290634,RMVar_hsa_circ_145198,RMVar_hsa_circ_145200,RMVar_hsa_circ_306391,RMVar_hsa_circ_145195,RMVar_hsa_circ_145196,RMVar_hsa_circ_329132,RMVar_hsa_circ_145202,RMVar_hsa_circ_291241,RMVar_hsa_circ_145201,RMVar_hsa_circ_145199 23130 RMVar_ID_23130 Human_SNP_ID_442832774 A-to-I Human chr10 + 94509280 94509280 94509280 GTGCGCTCCACCATGCCCGGCTAATTTTTAGTAGAGACAGGGTTTCACCGTGTTGGTCAGGCTGG GTGCGCTCCACCATGCCCGGCTAATTTTTAGTGGAGACAGGGTTTCACCGTGTTGGTCAGGCTGG A G TBC1D12,HELLS Ensembl:ENSG00000108239,Ensembl:ENSG00000119969 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs901010948 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_145167,RMVar_hsa_circ_290782,RMVar_hsa_circ_329268,RMVar_hsa_circ_283336,RMVar_hsa_circ_145163,RMVar_hsa_circ_145165,RMVar_hsa_circ_145166,RMVar_hsa_circ_145164,RMVar_hsa_circ_145162,RMVar_hsa_circ_316167,RMVar_hsa_circ_295649,RMVar_hsa_circ_145179,RMVar_hsa_circ_145180,RMVar_hsa_circ_339997,RMVar_hsa_circ_285903,RMVar_hsa_circ_333606,RMVar_hsa_circ_145197,RMVar_hsa_circ_145189,RMVar_hsa_circ_145190,RMVar_hsa_circ_145187,RMVar_hsa_circ_145188,RMVar_hsa_circ_316644,RMVar_hsa_circ_145186,RMVar_hsa_circ_295980,RMVar_hsa_circ_272113,RMVar_hsa_circ_290634,RMVar_hsa_circ_145198,RMVar_hsa_circ_145206,RMVar_hsa_circ_145200,RMVar_hsa_circ_145196,RMVar_hsa_circ_329132,RMVar_hsa_circ_291241,RMVar_hsa_circ_145201,RMVar_hsa_circ_293273,RMVar_hsa_circ_309831,RMVar_hsa_circ_145199,RMVar_hsa_circ_294620,RMVar_hsa_circ_272048,RMVar_hsa_circ_145204,RMVar_hsa_circ_145205,RMVar_hsa_circ_145203 23131 RMVar_ID_23131 Human_SNP_ID_442843288 A-to-I Human chr10 + 94550743 94550743 94550743 GAAACCCCATCTCTACAAAAAATTAAAAAACTAGCCGGCATGGTGGCACGCGCCTATAGTCCTAG GAAACCCCATCTCTACAAAAAATTAAAAAACTTGCCGGCATGGTGGCACGCGCCTATAGTCCTAG A T HELLS Ensembl:ENSG00000119969 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs952980121 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77960,RMVar_hsa_circ_145215,RMVar_hsa_circ_362221 23132 RMVar_ID_23132 Human_SNP_ID_442843300 A-to-I Human chr10 + 94550766 94550766 94550766 TAAAAAACTAGCCGGCATGGTGGCACGCGCCTATAGTCCTAGCTACTCAAGAGGGTGAGGCAGGA TAAAAAACTAGCCGGCATGGTGGCACGCGCCTGTAGTCCTAGCTACTCAAGAGGGTGAGGCAGGA A G HELLS Ensembl:ENSG00000119969 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1339486893 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11469445 RMVar_hsa_circ_77960,RMVar_hsa_circ_145215,RMVar_hsa_circ_362221 23133 RMVar_ID_23133 Human_SNP_ID_442844614 A-to-I Human chr10 + 94555653 94555652 94555654 TCTTTCTTTCTTTCTTTCTTTTTTTTGGAGACAGAGTCTTACTCTGTTGCCCAGGCTGGTGTGCA TCTTTCTTTCTTTCTTTCTTTTTTTTGGAGAC__AGTCTTACTCTGTTGCCCAGGCTGGTGTGCA CAG C HELLS Ensembl:ENSG00000119969 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1307008687 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_38905,RMVar_hsa_circ_319835,RMVar_hsa_circ_365551,RMVar_hsa_circ_319734 23134 RMVar_ID_23134 Human_SNP_ID_442844616 A-to-I Human chr10 + 94555655 94555655 94555655 TTTCTTTCTTTCTTTCTTTTTTTTGGAGACAGAGTCTTACTCTGTTGCCCAGGCTGGTGTGCAGT TTTCTTTCTTTCTTTCTTTTTTTTGGAGACAGGGTCTTACTCTGTTGCCCAGGCTGGTGTGCAGT A G HELLS Ensembl:ENSG00000119969 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985779671 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38905,RMVar_hsa_circ_319835,RMVar_hsa_circ_365551,RMVar_hsa_circ_319734 23135 RMVar_ID_23135 Human_SNP_ID_442845381 A-to-I Human chr10 + 94558808 94558808 94558808 TATTTTCAGTAGAGACAGAGTTTTACTGTGTTAGCCACGATGGTCTCCATCTCCTGACCTTGTGA TATTTTCAGTAGAGACAGAGTTTTACTGTGTTGGCCACGATGGTCTCCATCTCCTGACCTTGTGA A G HELLS Ensembl:ENSG00000119969 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs900318552 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38905,RMVar_hsa_circ_319835,RMVar_hsa_circ_365551 23136 RMVar_ID_23136 Human_SNP_ID_442845747 A-to-I Human chr10 + 94560206 94560206 94560206 AGCACCTGCCAGCACACCCGGCTAATTTTTGTATTTTTAGAAGAGACAGGGTTTCACCATCTTGG AGCACCTGCCAGCACACCCGGCTAATTTTTGTGTTTTTAGAAGAGACAGGGTTTCACCATCTTGG A G HELLS Ensembl:ENSG00000119969 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs761672083 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38905,RMVar_hsa_circ_319835,RMVar_hsa_circ_365551 23137 RMVar_ID_23137 Human_SNP_ID_442845748 A-to-I Human chr10 + 94560212 94560212 94560212 TGCCAGCACACCCGGCTAATTTTTGTATTTTTAGAAGAGACAGGGTTTCACCATCTTGGCCAGGC TGCCAGCACACCCGGCTAATTTTTGTATTTTTGGAAGAGACAGGGTTTCACCATCTTGGCCAGGC A G HELLS Ensembl:ENSG00000119969 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs996299236 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38905,RMVar_hsa_circ_319835,RMVar_hsa_circ_365551 23138 RMVar_ID_23138 Human_SNP_ID_442845794 A-to-I Human chr10 + 94560437 94560437 94560437 GGTAATACTGCTAGGTGTGGTGGCTCACGCCTATAATCCCAACACTTTGGGAGGCTGAGGCAGAT GGTAATACTGCTAGGTGTGGTGGCTCACGCCTCTAATCCCAACACTTTGGGAGGCTGAGGCAGAT A C HELLS Ensembl:ENSG00000119969 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs549526057 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38905,RMVar_hsa_circ_319835,RMVar_hsa_circ_365551 23139 RMVar_ID_23139 Human_SNP_ID_442845795 A-to-I Human chr10 + 94560437 94560437 94560437 GGTAATACTGCTAGGTGTGGTGGCTCACGCCTATAATCCCAACACTTTGGGAGGCTGAGGCAGAT GGTAATACTGCTAGGTGTGGTGGCTCACGCCTGTAATCCCAACACTTTGGGAGGCTGAGGCAGAT A G HELLS Ensembl:ENSG00000119969 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs549526057 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38905,RMVar_hsa_circ_319835,RMVar_hsa_circ_365551 23140 RMVar_ID_23140 Human_SNP_ID_442846222 A-to-I Human chr10 + 94562216 94562216 94562216 ACCTGAGGTCAGAAATTCAAGACTAGCTGGCCAACGTGGTGAAACCCCATCTCTACTAAAAATAC ACCTGAGGTCAGAAATTCAAGACTAGCTGGCCGACGTGGTGAAACCCCATCTCTACTAAAAATAC A G HELLS Ensembl:ENSG00000119969 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1045641742 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38905,RMVar_hsa_circ_319835,RMVar_hsa_circ_365551 23141 RMVar_ID_23141 Human_SNP_ID_442846857 A-to-I Human chr10 + 94564778 94564778 94564778 TGGGATTACAGGTACCTATTTGTATTTTTAGTAGAGACAGGGTTTTGCCATGTTGGCCAGGATGG TGGGATTACAGGTACCTATTTGTATTTTTAGTGGAGACAGGGTTTTGCCATGTTGGCCAGGATGG A G HELLS Ensembl:ENSG00000119969 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs944534585 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9616312,Human_RBP_ID_11469928,Human_RBP_ID_24862409 RMVar_hsa_circ_319835,RMVar_hsa_circ_378957 23142 RMVar_ID_23142 Human_SNP_ID_442846934 A-to-I Human chr10 + 94565065 94565065 94565065 CACTGAAAAATAATCGTCAGGGGGCCGGGAGCAGTGGCTCACGCCTGTAATCCCAGCATTTTGGG CACTGAAAAATAATCGTCAGGGGGCCGGGAGCGGTGGCTCACGCCTGTAATCCCAGCATTTTGGG A G HELLS Ensembl:ENSG00000119969 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs944584639 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_319835,RMVar_hsa_circ_378957 23143 RMVar_ID_23143 Human_SNP_ID_442846974 A-to-I Human chr10 + 94565175 94565175 94565175 TCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATATAAAAATTAGCTGGGAATGGTGGCTT TCTGGCCAACATGGTGAAACCCCGTCTCTACTGAAAATATAAAAATTAGCTGGGAATGGTGGCTT A G HELLS Ensembl:ENSG00000119969 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs908522212 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_319835,RMVar_hsa_circ_378957 23144 RMVar_ID_23144 Human_SNP_ID_442847042 A-to-I Human chr10 + 94565433 94565433 94565433 CTTTTAGGCTGGGCGTGGTGGCTCATACCTGTAAACCCCGGCGCTTTGGGAGGCCAAGGTGGGAG CTTTTAGGCTGGGCGTGGTGGCTCATACCTGTGAACCCCGGCGCTTTGGGAGGCCAAGGTGGGAG A G HELLS Ensembl:ENSG00000119969 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1259461704 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17559121,Human_RBP_ID_24862419 RMVar_hsa_circ_319835,RMVar_hsa_circ_378957 23145 RMVar_ID_23145 Human_SNP_ID_442847220 A-to-I Human chr10 + 94566076 94566076 94566076 CACCAGGCCTGGCTGATTTTTGTATTTTTTGTAGAGATGGGGTTTTGTCATGTTGTCTAGGCTGG CACCAGGCCTGGCTGATTTTTGTATTTTTTGTGGAGATGGGGTTTTGTCATGTTGTCTAGGCTGG A G HELLS Ensembl:ENSG00000119969 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1488536777 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9616335,Human_RBP_ID_11470003,Human_RBP_ID_22885972,Human_RBP_ID_24847878 RMVar_hsa_circ_319835,RMVar_hsa_circ_378957 23146 RMVar_ID_23146 Human_SNP_ID_442847239 A-to-I Human chr10 + 94566158 94566158 94566158 CCTGCCTCGGCCTCCCAGAGTACTGGGATTACAGGTCTGAGCCACTGTGTCCGGTTGGGAATTGG CCTGCCTCGGCCTCCCAGAGTACTGGGATTACGGGTCTGAGCCACTGTGTCCGGTTGGGAATTGG A G HELLS Ensembl:ENSG00000119969 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1013406967 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225780,Human_RBP_ID_748542,Human_RBP_ID_6018692,Human_RBP_ID_11470010,Human_RBP_ID_24847882 RMVar_hsa_circ_319835,RMVar_hsa_circ_378957 23147 RMVar_ID_23147 Human_SNP_ID_442847643 A-to-I Human chr10 + 94567753 94567753 94567753 CATGGCGAAATCCTGTCTCTACAAAAAGAAATACAGAAATAGCCAGGTGTGGTGGTGCATGACTT CATGGCGAAATCCTGTCTCTACAAAAAGAAATGCAGAAATAGCCAGGTGTGGTGGTGCATGACTT A G HELLS Ensembl:ENSG00000119969 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1176216188 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11470120,Human_RBP_ID_24847940 RMVar_hsa_circ_319835,RMVar_hsa_circ_378957 23148 RMVar_ID_23148 Human_SNP_ID_442848129 A-to-I Human chr10 + 94569404 94569404 94569404 CAGGGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTCCTGACCTTGTGATTTGCCTGACTTGGC CAGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTTGTGATTTGCCTGACTTGGC A G HELLS Ensembl:ENSG00000119969 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs986983238 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11470203,Human_RBP_ID_24847999 RMVar_hsa_circ_319835,RMVar_hsa_circ_378957 23149 RMVar_ID_23149 Human_SNP_ID_442848323 A-to-I Human chr10 + 94570141 94570141 94570141 CTCGGCTCATTGAACCTCTGATTGCTGGGCTCAAGCAATCCTCCCACCTCATCCTCCTGAGTAGC CTCGGCTCATTGAACCTCTGATTGCTGGGCTCGAGCAATCCTCCCACCTCATCCTCCTGAGTAGC A G HELLS Ensembl:ENSG00000119969 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1409206019 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8342229,Human_RBP_ID_11470246 RMVar_hsa_circ_319835,RMVar_hsa_circ_378957 23150 RMVar_ID_23150 Human_SNP_ID_442848325 A-to-I Human chr10 + 94570145 94570145 94570145 GCTCATTGAACCTCTGATTGCTGGGCTCAAGCAATCCTCCCACCTCATCCTCCTGAGTAGCTGGG GCTCATTGAACCTCTGATTGCTGGGCTCAAGCGATCCTCCCACCTCATCCTCCTGAGTAGCTGGG A G HELLS Ensembl:ENSG00000119969 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1165602583 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8342229,Human_RBP_ID_11470246,Human_RBP_ID_24862472 RMVar_hsa_circ_319835,RMVar_hsa_circ_378957 23151 RMVar_ID_23151 Human_SNP_ID_442850221 A-to-I Human chr10 + 94577671 94577671 94577671 AAACCAGGCCGGGCATGAAGGCTTATGCCAGTAATTCCAGCACTTGGGAGTCTGAGGTGGGCAGA AAACCAGGCCGGGCATGAAGGCTTATGCCAGTGATTCCAGCACTTGGGAGTCTGAGGTGGGCAGA A G HELLS,AL138759.1 Ensembl:ENSG00000119969,Ensembl:ENSG00000244332 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs949846270 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5245884,Human_RBP_ID_11470676,Human_RBP_ID_18600926,Human_RBP_ID_22789123,Human_RBP_ID_24862551 RMVar_hsa_circ_26477,RMVar_hsa_circ_63756,RMVar_hsa_circ_49890,RMVar_hsa_circ_61334,RMVar_hsa_circ_18197,RMVar_hsa_circ_291553,RMVar_hsa_circ_304109,RMVar_hsa_circ_145216,RMVar_hsa_circ_145217 23152 RMVar_ID_23152 Human_SNP_ID_442850316 A-to-I Human chr10 + 94577948 94577929 94577948 AGCCGGGCGCGGTGGCGGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCG AGCCGGGCGCGGTG___________________GCTACTCGGGAGGCTGAGGCAGGAGAATGGCG GGCGGGCGCCTGTAGTCCCA G HELLS,AL138759.1 Ensembl:ENSG00000119969,Ensembl:ENSG00000244332 Protein coding,lincRNA intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1227281299 Functional Loss DEL dbSNP153 15..33 33 - - - RMVar_hsa_circ_26477,RMVar_hsa_circ_63756,RMVar_hsa_circ_49890,RMVar_hsa_circ_61334,RMVar_hsa_circ_18197,RMVar_hsa_circ_291553,RMVar_hsa_circ_304109,RMVar_hsa_circ_145216,RMVar_hsa_circ_145217 23153 RMVar_ID_23153 Human_SNP_ID_442850516 A-to-I Human chr10 + 94578441 94578441 94578441 TAATAGGGCTGGCCGTAGTGGCTCACCCCTGTAATCCCAGCACTTTGGGAAGCTTAGGCGGGCAG TAATAGGGCTGGCCGTAGTGGCTCACCCCTGTCATCCCAGCACTTTGGGAAGCTTAGGCGGGCAG A C HELLS,AL138759.1 Ensembl:ENSG00000119969,Ensembl:ENSG00000244332 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs923120696 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26477,RMVar_hsa_circ_63756,RMVar_hsa_circ_49890,RMVar_hsa_circ_61334,RMVar_hsa_circ_18197,RMVar_hsa_circ_291553,RMVar_hsa_circ_304109,RMVar_hsa_circ_145216,RMVar_hsa_circ_145217 23154 RMVar_ID_23154 Human_SNP_ID_442850527 A-to-I Human chr10 + 94578472 94578472 94578472 TAATCCCAGCACTTTGGGAAGCTTAGGCGGGCAGATCACTTGAGGTGAGGAGTTTGAGACCATCC TAATCCCAGCACTTTGGGAAGCTTAGGCGGGCGGATCACTTGAGGTGAGGAGTTTGAGACCATCC A G HELLS,AL138759.1 Ensembl:ENSG00000119969,Ensembl:ENSG00000244332 Protein coding,lincRNA intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs986705565 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8245900,Human_RBP_ID_11470705,Human_RBP_ID_24862558 RMVar_hsa_circ_26477,RMVar_hsa_circ_63756,RMVar_hsa_circ_49890,RMVar_hsa_circ_61334,RMVar_hsa_circ_18197,RMVar_hsa_circ_291553,RMVar_hsa_circ_304109,RMVar_hsa_circ_145216,RMVar_hsa_circ_145217 23155 RMVar_ID_23155 Human_SNP_ID_442850545 A-to-I Human chr10 + 94578571 94578571 94578571 TCTCTACAAAAATACAAAAATTACCTGGGCATAGTGGCCTAGCTCCTTGGGAGGCTGAGGCAGGA TCTCTACAAAAATACAAAAATTACCTGGGCATGGTGGCCTAGCTCCTTGGGAGGCTGAGGCAGGA A G HELLS,AL138759.1 Ensembl:ENSG00000119969,Ensembl:ENSG00000244332 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs757577540 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5245922,Human_RBP_ID_6018945,Human_RBP_ID_24862560 RMVar_hsa_circ_26477,RMVar_hsa_circ_63756,RMVar_hsa_circ_49890,RMVar_hsa_circ_61334,RMVar_hsa_circ_18197,RMVar_hsa_circ_291553,RMVar_hsa_circ_304109,RMVar_hsa_circ_145216,RMVar_hsa_circ_145217 23156 RMVar_ID_23156 Human_SNP_ID_442850750 A-to-I Human chr10 + 94579220 94579218 94579220 CTACTACTTTTTTCTTTTTTTTTTTTTTTTTGAGGCAGAGTCTTGCTCTGTTGCCCAGGCTGGAG CTACTACTTTTTTCTTTTTTTTTTTTTTTTT__GGCAGAGTCTTGCTCTGTTGCCCAGGCTGGAG TGA T HELLS,AL138759.1 Ensembl:ENSG00000119969,Ensembl:ENSG00000244332 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1476624099 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_11470736 RMVar_hsa_circ_26477,RMVar_hsa_circ_63756,RMVar_hsa_circ_49890,RMVar_hsa_circ_61334,RMVar_hsa_circ_18197,RMVar_hsa_circ_291553,RMVar_hsa_circ_304109,RMVar_hsa_circ_145216,RMVar_hsa_circ_145217 23157 RMVar_ID_23157 Human_SNP_ID_442850852 A-to-I Human chr10 + 94579603 94579603 94579603 TCACTTTGTCACCCAGGCTGGAGTCCTGTGGCACGATCTCAGCTCACTGTAGCCTGAATCTCCTG TCACTTTGTCACCCAGGCTGGAGTCCTGTGGCTCGATCTCAGCTCACTGTAGCCTGAATCTCCTG A T HELLS,AL138759.1 Ensembl:ENSG00000119969,Ensembl:ENSG00000244332 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1220326780 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225594,Human_RBP_ID_11470742,Human_RBP_ID_24848344 RMVar_hsa_circ_26477,RMVar_hsa_circ_63756,RMVar_hsa_circ_49890,RMVar_hsa_circ_61334,RMVar_hsa_circ_18197,RMVar_hsa_circ_291553,RMVar_hsa_circ_304109,RMVar_hsa_circ_145216,RMVar_hsa_circ_145217 23158 RMVar_ID_23158 Human_SNP_ID_442850865 A-to-I Human chr10 + 94579654 94579654 94579654 GCCTGAATCTCCTGGGCTCAAGTGATTCTCCTACCTCTGTCTCCTGAGTAGCCGGGACTACAGGC GCCTGAATCTCCTGGGCTCAAGTGATTCTCCTGCCTCTGTCTCCTGAGTAGCCGGGACTACAGGC A G HELLS,AL138759.1 Ensembl:ENSG00000119969,Ensembl:ENSG00000244332 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1311268715 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6018969,Human_RBP_ID_8245827,Human_RBP_ID_11470742,Human_RBP_ID_24848347 RMVar_hsa_circ_26477,RMVar_hsa_circ_63756,RMVar_hsa_circ_49890,RMVar_hsa_circ_61334,RMVar_hsa_circ_18197,RMVar_hsa_circ_291553,RMVar_hsa_circ_304109,RMVar_hsa_circ_145216,RMVar_hsa_circ_145217 23159 RMVar_ID_23159 Human_SNP_ID_442853296 A-to-I Human chr10 + 94588601 94588601 94588601 TGGCATTTCGCCATGTTTCCCAGGTTGGTCTCAGACTCCTGGGCTTAAGCAGTCCACCCACCTTG TGGCATTTCGCCATGTTTCCCAGGTTGGTCTCCGACTCCTGGGCTTAAGCAGTCCACCCACCTTG A C HELLS,AL138759.1 Ensembl:ENSG00000119969,Ensembl:ENSG00000244332 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs554757042 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17559125 RMVar_hsa_circ_17601,RMVar_hsa_circ_49890,RMVar_hsa_circ_61334,RMVar_hsa_circ_18197,RMVar_hsa_circ_291553,RMVar_hsa_circ_145217,RMVar_hsa_circ_90366,RMVar_hsa_circ_145219,RMVar_hsa_circ_50723,RMVar_hsa_circ_145218,RMVar_hsa_circ_293361,RMVar_hsa_circ_344424,RMVar_hsa_circ_145220,RMVar_hsa_circ_145221 23160 RMVar_ID_23160 Human_SNP_ID_442853297 A-to-I Human chr10 + 94588601 94588601 94588601 TGGCATTTCGCCATGTTTCCCAGGTTGGTCTCAGACTCCTGGGCTTAAGCAGTCCACCCACCTTG TGGCATTTCGCCATGTTTCCCAGGTTGGTCTCTGACTCCTGGGCTTAAGCAGTCCACCCACCTTG A T HELLS,AL138759.1 Ensembl:ENSG00000119969,Ensembl:ENSG00000244332 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs554757042 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17559125 RMVar_hsa_circ_17601,RMVar_hsa_circ_49890,RMVar_hsa_circ_61334,RMVar_hsa_circ_18197,RMVar_hsa_circ_291553,RMVar_hsa_circ_145217,RMVar_hsa_circ_90366,RMVar_hsa_circ_145219,RMVar_hsa_circ_50723,RMVar_hsa_circ_145218,RMVar_hsa_circ_293361,RMVar_hsa_circ_344424,RMVar_hsa_circ_145220,RMVar_hsa_circ_145221 23161 RMVar_ID_23161 Human_SNP_ID_442857506 A-to-I Human chr10 + 94605266 94605266 94605266 CACCATGCCCAGCTAATTTTTGTATTTTTAGTAGGGACAGGGTTTCACCATGTTGGCCACGCTGG CACCATGCCCAGCTAATTTTTGTATTTTTAGTGGGGACAGGGTTTCACCATGTTGGCCACGCTGG A G HELLS,AL138759.1 Ensembl:ENSG00000119969,Ensembl:ENSG00000244332 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs187476131 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8245157,Human_RBP_ID_11471966,Human_RBP_ID_24849025 RMVar_hsa_circ_145219 23162 RMVar_ID_23162 Human_SNP_ID_442857527 A-to-I Human chr10 + 94605344 94605344 94605344 ACCTCAGGTGATCCACCCTCCTCGGCCTCCCAAAGTGTTGGTACTACAGGTGTGAGCCACTGCGC ACCTCAGGTGATCCACCCTCCTCGGCCTCCCAGAGTGTTGGTACTACAGGTGTGAGCCACTGCGC A G HELLS,AL138759.1 Ensembl:ENSG00000119969,Ensembl:ENSG00000244332 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1445622950 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_385727,Human_RBP_ID_8245834,Human_RBP_ID_9616798,Human_RBP_ID_11471968,Human_RBP_ID_19453379,Human_RBP_ID_23478394,Human_RBP_ID_24862751 RMVar_hsa_circ_145219 23163 RMVar_ID_23163 Human_SNP_ID_442857801 A-to-I Human chr10 + 94606420 94606420 94606420 GTTGGAGAGCAGTGGTGCAACTATAGCTCACTACATTCTTGAATTTCTGGGCTCAAGCCATCTTC GTTGGAGAGCAGTGGTGCAACTATAGCTCACTGCATTCTTGAATTTCTGGGCTCAAGCCATCTTC A G HELLS,AL138759.1 Ensembl:ENSG00000119969,Ensembl:ENSG00000244332 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1368620455 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1160509,Human_RBP_ID_1773678,Human_RBP_ID_6019540,Human_RBP_ID_11472041,Human_RBP_ID_18245542,Human_RBP_ID_19569069,Human_RBP_ID_24849066,Human_RBP_ID_27612782 RMVar_hsa_circ_145219 23164 RMVar_ID_23164 Human_SNP_ID_442858161 A-to-I Human chr10 + 94607972 94607972 94607972 CTGGTCCCGAACTGATCTCAGGTGATCTGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAAGC CTGGTCCCGAACTGATCTCAGGTGATCTGCCCCCCTCGGCCTCCCAAAGTGCTGGGATTACAAGC A C HELLS,AL138759.1 Ensembl:ENSG00000119969,Ensembl:ENSG00000244332 Protein coding,lincRNA CDS,intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs1238055979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11472167,Human_RBP_ID_24849125 Human_Splice_Rec_1162004,Human_Splice_Rec_1162005 RMVar_hsa_circ_145219 23165 RMVar_ID_23165 Human_SNP_ID_442858162 A-to-I Human chr10 + 94607972 94607972 94607972 CTGGTCCCGAACTGATCTCAGGTGATCTGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAAGC CTGGTCCCGAACTGATCTCAGGTGATCTGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAAGC A G HELLS,AL138759.1 Ensembl:ENSG00000119969,Ensembl:ENSG00000244332 Protein coding,lincRNA CDS,intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs1238055979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11472167,Human_RBP_ID_24849125 Human_Splice_Rec_1162004,Human_Splice_Rec_1162005 RMVar_hsa_circ_145219 23166 RMVar_ID_23166 Human_SNP_ID_442858172 A-to-I Human chr10 + 94607986 94607986 94607986 ATCTCAGGTGATCTGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAAGCGTGAGCCACTGCGT ATCTCAGGTGATCTGCCCACCTCGGCCTCCCAGAGTGCTGGGATTACAAGCGTGAGCCACTGCGT A G HELLS,AL138759.1 Ensembl:ENSG00000119969,Ensembl:ENSG00000244332 Protein coding,lincRNA CDS,intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,31158229,31158229 RNA-Seq:(High) rs575662198 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1162004,Human_Splice_Rec_1162005 RMVar_hsa_circ_145219 23167 RMVar_ID_23167 Human_SNP_ID_442858786 A-to-I Human chr10 + 94610335 94610335 94610335 AAATAAATGAGGCCGGGCGCAGTGGTGCCTGTAATCCCAGCAGTTTGGGAGGCTGAGGCTAGTGG AAATAAATGAGGCCGGGCGCAGTGGTGCCTGTCATCCCAGCAGTTTGGGAGGCTGAGGCTAGTGG A C HELLS,AL138759.1 Ensembl:ENSG00000119969,Ensembl:ENSG00000244332 Protein coding,lincRNA 3'UTR,intron GSE38233;GSE100210;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,29129909,31158229,31158229 RNA-Seq:(High) rs1478785870 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225600,Human_RBP_ID_5086723,Human_RBP_ID_5165126,Human_RBP_ID_6019672,Human_RBP_ID_8173590,Human_RBP_ID_8245024,Human_RBP_ID_26398548 RMVar_hsa_circ_145219 23168 RMVar_ID_23168 Human_SNP_ID_442858793 A-to-I Human chr10 + 94610363 94610363 94610363 CTGTAATCCCAGCAGTTTGGGAGGCTGAGGCTAGTGGATCATGTGGCCGAGATCGCGTCACTGCA CTGTAATCCCAGCAGTTTGGGAGGCTGAGGCTGGTGGATCATGTGGCCGAGATCGCGTCACTGCA A G HELLS,AL138759.1 Ensembl:ENSG00000119969,Ensembl:ENSG00000244332 Protein coding,lincRNA 3'UTR,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs766277220 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5086723,Human_RBP_ID_6019673,Human_RBP_ID_11472347,Human_RBP_ID_24862806,Human_RBP_ID_26397896 RMVar_hsa_circ_145219 23169 RMVar_ID_23169 Human_SNP_ID_442858811 A-to-I Human chr10 + 94610405 94610405 94610405 GTGGCCGAGATCGCGTCACTGCACTCCAGTCTAGCAACAGAGCGATACCTTGTTTCTTACTTAAA GTGGCCGAGATCGCGTCACTGCACTCCAGTCTGGCAACAGAGCGATACCTTGTTTCTTACTTAAA A G HELLS,AL138759.1 Ensembl:ENSG00000119969,Ensembl:ENSG00000244332 Protein coding,lincRNA 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1247420621 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_385773,Human_RBP_ID_3362123,Human_RBP_ID_6019673,Human_RBP_ID_24849206 RMVar_hsa_circ_145219 23170 RMVar_ID_23170 Human_SNP_ID_442858874 A-to-I Human chr10 + 94610632 94610632 94610632 TTTTCTCAGATGGAGTTCTGCTCTTGTCGCCCAGACTGGAGTGCAATGGCACGATGTTGGCTCAC TTTTCTCAGATGGAGTTCTGCTCTTGTCGCCCGGACTGGAGTGCAATGGCACGATGTTGGCTCAC A G HELLS,AL138759.1 Ensembl:ENSG00000119969,Ensembl:ENSG00000244332 Protein coding,lincRNA 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1319604346 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_385774,Human_RBP_ID_3365947,Human_RBP_ID_6019675,Human_RBP_ID_11472367 RMVar_hsa_circ_145219 23171 RMVar_ID_23171 Human_SNP_ID_442858894 A-to-I Human chr10 + 94610688 94610688 94610688 TTGGCTCACTGCAATCTCCGCTTCCCAGGTTCAAGCAGTTCTCCAGCCTTAGCCTCCCAAGTAGC TTGGCTCACTGCAATCTCCGCTTCCCAGGTTCGAGCAGTTCTCCAGCCTTAGCCTCCCAAGTAGC A G HELLS,AL138759.1 Ensembl:ENSG00000119969,Ensembl:ENSG00000244332 Protein coding,lincRNA 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1219366644 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4133298,Human_RBP_ID_9616909,Human_RBP_ID_11472373,Human_RBP_ID_22886199,Human_RBP_ID_24862809 RMVar_hsa_circ_145219 23172 RMVar_ID_23172 Human_SNP_ID_442859355 A-to-I Human chr10 + 94612730 94612730 94612730 AACGGATCACTTGAGGCCAGGAGTTTGAAACTAGTCTGGTCAACATGGTGAAACCCCGTCTCCAC AACGGATCACTTGAGGCCAGGAGTTTGAAACTGGTCTGGTCAACATGGTGAAACCCCGTCTCCAC A G HELLS Ensembl:ENSG00000119969 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs918781997 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9616955,Human_RBP_ID_11472529,Human_RBP_ID_17559128,Human_RBP_ID_24849278,Human_RBP_ID_26397901 23173 RMVar_ID_23173 Human_SNP_ID_442859358 A-to-I Human chr10 + 94612742 94612742 94612742 GAGGCCAGGAGTTTGAAACTAGTCTGGTCAACATGGTGAAACCCCGTCTCCACTAAAACAAAAAG GAGGCCAGGAGTTTGAAACTAGTCTGGTCAACCTGGTGAAACCCCGTCTCCACTAAAACAAAAAG A C HELLS Ensembl:ENSG00000119969 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs951547343 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9616955,Human_RBP_ID_11472530,Human_RBP_ID_17559128,Human_RBP_ID_19569288,Human_RBP_ID_24849278,Human_RBP_ID_26397901 23174 RMVar_ID_23174 Human_SNP_ID_442859359 A-to-I Human chr10 + 94612742 94612742 94612742 GAGGCCAGGAGTTTGAAACTAGTCTGGTCAACATGGTGAAACCCCGTCTCCACTAAAACAAAAAG GAGGCCAGGAGTTTGAAACTAGTCTGGTCAACGTGGTGAAACCCCGTCTCCACTAAAACAAAAAG A G HELLS Ensembl:ENSG00000119969 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs951547343 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9616955,Human_RBP_ID_11472530,Human_RBP_ID_17559128,Human_RBP_ID_19569288,Human_RBP_ID_24849278,Human_RBP_ID_26397901 23175 RMVar_ID_23175 Human_SNP_ID_442859367 A-to-I Human chr10 + 94612765 94612765 94612765 CTGGTCAACATGGTGAAACCCCGTCTCCACTAAAACAAAAAGTTTTCTGGATGTGGTGGCACACA CTGGTCAACATGGTGAAACCCCGTCTCCACTACAACAAAAAGTTTTCTGGATGTGGTGGCACACA A C HELLS Ensembl:ENSG00000119969 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1212913661 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6035291,Human_RBP_ID_8995477,Human_RBP_ID_9616956,Human_RBP_ID_11472530,Human_RBP_ID_17461796,Human_RBP_ID_17559128,Human_RBP_ID_22789259,Human_RBP_ID_23153302,Human_RBP_ID_26397902 23176 RMVar_ID_23176 Human_SNP_ID_442859374 A-to-I Human chr10 + 94612815 94612815 94612815 ATGTGGTGGCACACATACCTGTAATCCCAGCTACTTTGGTGGCTGAGGCATGAGAATCACTTGAA ATGTGGTGGCACACATACCTGTAATCCCAGCTGCTTTGGTGGCTGAGGCATGAGAATCACTTGAA A G HELLS Ensembl:ENSG00000119969 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229,31158229 RNA-Seq:(High) rs914211238 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1773742,Human_RBP_ID_11472536,Human_RBP_ID_17559129,Human_RBP_ID_26397903 23177 RMVar_ID_23177 Human_SNP_ID_443042456 A-to-I Human chr10 - 95269415 95269415 95269415 GGCGTATGCCACCACACCCGGCTAATTTTTGTATTTTTAGTGGAGATGGGGTTTCACCATGTTGG GGCGTATGCCACCACACCCGGCTAATTTTTGTGTTTTTAGTGGAGATGGGGTTTCACCATGTTGG T C PDLIM1 Ensembl:ENSG00000107438 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs545547132 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106573,RMVar_hsa_circ_115700,RMVar_hsa_circ_145232,RMVar_hsa_circ_145231,RMVar_hsa_circ_325104,RMVar_hsa_circ_145238 23178 RMVar_ID_23178 Human_SNP_ID_443042856 A-to-I Human chr10 - 95271023 95271023 95271023 TGTCCTGGCCAGGTGCGGTGGCTCTCTTTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGACAAA TGTCCTGGCCAGGTGCGGTGGCTCTCTTTGTAGTCCCAGCACTTTGGGAGGCCGAGGCAGACAAA T C PDLIM1 Ensembl:ENSG00000107438 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1010957068 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106573,RMVar_hsa_circ_115700,RMVar_hsa_circ_145232,RMVar_hsa_circ_145231,RMVar_hsa_circ_325104,RMVar_hsa_circ_145238 23179 RMVar_ID_23179 Human_SNP_ID_443042857 A-to-I Human chr10 - 95271024 95271024 95271024 ATGTCCTGGCCAGGTGCGGTGGCTCTCTTTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGACAA ATGTCCTGGCCAGGTGCGGTGGCTCTCTTTGTGATCCCAGCACTTTGGGAGGCCGAGGCAGACAA T C PDLIM1 Ensembl:ENSG00000107438 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs371408037 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106573,RMVar_hsa_circ_115700,RMVar_hsa_circ_145232,RMVar_hsa_circ_145231,RMVar_hsa_circ_325104,RMVar_hsa_circ_145238 23180 RMVar_ID_23180 Human_SNP_ID_443055094 A-to-I Human chr10 - 95323822 95323822 95323822 GCCACATCCAGCTAATTTTTGTATTTTTTTGTAGAGATGGGGTTTTGCTTTGTTGCCCAGGCTGG GCCACATCCAGCTAATTTTTGTATTTTTTTGTGGAGATGGGGTTTTGCTTTGTTGCCCAGGCTGG T C SORBS1 Ensembl:ENSG00000095637 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1307242930 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_145241,RMVar_hsa_circ_297829,RMVar_hsa_circ_349599,RMVar_hsa_circ_355944,RMVar_hsa_circ_34088,RMVar_hsa_circ_43530,RMVar_hsa_circ_145242,RMVar_hsa_circ_145240 23181 RMVar_ID_23181 Human_SNP_ID_443070158 A-to-I Human chr10 - 95386920 95386920 95386920 TTTTGTAGAGATGGGATCTCGCTATGTTGCCCAGGCTGGTCTTGGGTTTCTGGCCTCAAGCAATC TTTTGTAGAGATGGGATCTCGCTATGTTGCCCGGGCTGGTCTTGGGTTTCTGGCCTCAAGCAATC T C SORBS1 Ensembl:ENSG00000095637 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1030572680 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_295121,RMVar_hsa_circ_67586,RMVar_hsa_circ_62526,RMVar_hsa_circ_145243,RMVar_hsa_circ_69240,RMVar_hsa_circ_363185,RMVar_hsa_circ_105463,RMVar_hsa_circ_65678,RMVar_hsa_circ_30997,RMVar_hsa_circ_145250,RMVar_hsa_circ_330916,RMVar_hsa_circ_145252,RMVar_hsa_circ_325722,RMVar_hsa_circ_145254,RMVar_hsa_circ_145253,RMVar_hsa_circ_324732,RMVar_hsa_circ_267072,RMVar_hsa_circ_359047,RMVar_hsa_circ_282590,RMVar_hsa_circ_61985,RMVar_hsa_circ_145257,RMVar_hsa_circ_24493,RMVar_hsa_circ_145256 23182 RMVar_ID_23182 Human_SNP_ID_443070216 A-to-I Human chr10 - 95387059 95387059 95387059 CAGGCTGGAGTGCAGTGGTACAGTCATAGCTCACTGCAGCCTCAAACTCCTAGACTCAAGCAATC CAGGCTGGAGTGCAGTGGTACAGTCATAGCTCTCTGCAGCCTCAAACTCCTAGACTCAAGCAATC T A SORBS1 Ensembl:ENSG00000095637 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1276662771 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1162636,Human_Splice_Rec_1162637,Human_Splice_Rec_1162910,Human_Splice_Rec_1162911 RMVar_hsa_circ_295121,RMVar_hsa_circ_67586,RMVar_hsa_circ_62526,RMVar_hsa_circ_145243,RMVar_hsa_circ_69240,RMVar_hsa_circ_363185,RMVar_hsa_circ_105463,RMVar_hsa_circ_65678,RMVar_hsa_circ_30997,RMVar_hsa_circ_145250,RMVar_hsa_circ_330916,RMVar_hsa_circ_145252,RMVar_hsa_circ_325722,RMVar_hsa_circ_145254,RMVar_hsa_circ_145253,RMVar_hsa_circ_324732,RMVar_hsa_circ_267072,RMVar_hsa_circ_359047,RMVar_hsa_circ_282590,RMVar_hsa_circ_61985,RMVar_hsa_circ_145257,RMVar_hsa_circ_24493,RMVar_hsa_circ_145256 23183 RMVar_ID_23183 Human_SNP_ID_443071062 A-to-I Human chr10 - 95390741 95390741 95390741 CCAGCTACTTGGGAGGCTGAGGCAAGAGAATCACTTGAATCTGGGATGCAGAGGTTGCAGTGAGC CCAGCTACTTGGGAGGCTGAGGCAAGAGAATCGCTTGAATCTGGGATGCAGAGGTTGCAGTGAGC T C SORBS1 Ensembl:ENSG00000095637 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1470172441 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_295121,RMVar_hsa_circ_67586,RMVar_hsa_circ_62526,RMVar_hsa_circ_145243,RMVar_hsa_circ_69240,RMVar_hsa_circ_363185,RMVar_hsa_circ_105463,RMVar_hsa_circ_65678,RMVar_hsa_circ_30997,RMVar_hsa_circ_145250,RMVar_hsa_circ_330916,RMVar_hsa_circ_145252,RMVar_hsa_circ_325722,RMVar_hsa_circ_145254,RMVar_hsa_circ_145253,RMVar_hsa_circ_324732,RMVar_hsa_circ_267072,RMVar_hsa_circ_359047,RMVar_hsa_circ_282590,RMVar_hsa_circ_61985,RMVar_hsa_circ_145257,RMVar_hsa_circ_24493,RMVar_hsa_circ_145256 23184 RMVar_ID_23184 Human_SNP_ID_443073026 A-to-I Human chr10 - 95399331 95399331 95399331 GTTGTGTTCCAGTAAAATCAGCCCATGGGCCAAAGTTTGCTGACCCCTGCTCTAAACAGAACTAA GTTGTGTTCCAGTAAAATCAGCCCATGGGCCAGAGTTTGCTGACCCCTGCTCTAAACAGAACTAA T C SORBS1 Ensembl:ENSG00000095637 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs778833375 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_295121,RMVar_hsa_circ_62526,RMVar_hsa_circ_145243,RMVar_hsa_circ_69240,RMVar_hsa_circ_363185,RMVar_hsa_circ_105463,RMVar_hsa_circ_65678,RMVar_hsa_circ_30997,RMVar_hsa_circ_145250,RMVar_hsa_circ_330916,RMVar_hsa_circ_145252,RMVar_hsa_circ_325722,RMVar_hsa_circ_145254,RMVar_hsa_circ_145253,RMVar_hsa_circ_324732,RMVar_hsa_circ_267072,RMVar_hsa_circ_359047,RMVar_hsa_circ_282590,RMVar_hsa_circ_61985,RMVar_hsa_circ_145258,RMVar_hsa_circ_145257,RMVar_hsa_circ_145256,RMVar_hsa_circ_323294,RMVar_hsa_circ_377421,RMVar_hsa_circ_362166,RMVar_hsa_circ_362489,RMVar_hsa_circ_354525 23185 RMVar_ID_23185 Human_SNP_ID_443077729 A-to-I Human chr10 - 95418218 95418218 95418218 CAAAAATTAGCCGGGTGTGGTGGCACAGGCCTATAGTCTCGGCTACTCAGGAGGCTGAGGCAGGA CAAAAATTAGCCGGGTGTGGTGGCACAGGCCTGTAGTCTCGGCTACTCAGGAGGCTGAGGCAGGA T C SORBS1 Ensembl:ENSG00000095637 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs532770477 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105463,RMVar_hsa_circ_30997,RMVar_hsa_circ_145250,RMVar_hsa_circ_267072,RMVar_hsa_circ_359047,RMVar_hsa_circ_145258,RMVar_hsa_circ_145256,RMVar_hsa_circ_377421 23186 RMVar_ID_23186 Human_SNP_ID_443120965 A-to-I Human chr10 - 95606004 95606004 95606004 TCGTCCTACCCTTTTCCTCCAAAACAAAAATTAGAGGATTATTTTAATACTTTGGATTCTTCCCC TCGTCCTACCCTTTTCCTCCAAAACAAAAATTGGAGGATTATTTTAATACTTTGGATTCTTCCCC T C ALDH18A1 Ensembl:ENSG00000059573 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1159715117 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_274126,Human_RBP_ID_385877,Human_RBP_ID_1773803,Human_RBP_ID_3362296,Human_RBP_ID_6020542,Human_RBP_ID_8172723,Human_RBP_ID_8995629,Human_RBP_ID_11501122,Human_RBP_ID_17680940,Human_RBP_ID_17785694,Human_RBP_ID_22886244,Human_RBP_ID_24458214,Human_RBP_ID_24849690,Human_RBP_ID_26398552,Human_RBP_ID_27196538 23187 RMVar_ID_23187 Human_SNP_ID_443127432 A-to-I Human chr10 - 95632480 95632480 95632480 ATGCGCCTGCGGTTCCAGCTACTCGGGGCTGAAGCAGAAGGTTCACTTGGAGCTGGGAGTTCCAG ATGCGCCTGCGGTTCCAGCTACTCGGGGCTGAGGCAGAAGGTTCACTTGGAGCTGGGAGTTCCAG T C ALDH18A1 Ensembl:ENSG00000059573 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971303457 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2240208 RMVar_hsa_circ_14907,RMVar_hsa_circ_269363,RMVar_hsa_circ_17352,RMVar_hsa_circ_55430,RMVar_hsa_circ_55685,RMVar_hsa_circ_50082,RMVar_hsa_circ_335446 23188 RMVar_ID_23188 Human_SNP_ID_443127438 A-to-I Human chr10 - 95632492 95632492 95632492 GGACATGGTGGTATGCGCCTGCGGTTCCAGCTACTCGGGGCTGAAGCAGAAGGTTCACTTGGAGC GGACATGGTGGTATGCGCCTGCGGTTCCAGCTCCTCGGGGCTGAAGCAGAAGGTTCACTTGGAGC T G ALDH18A1 Ensembl:ENSG00000059573 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1298886528 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14907,RMVar_hsa_circ_269363,RMVar_hsa_circ_17352,RMVar_hsa_circ_55430,RMVar_hsa_circ_55685,RMVar_hsa_circ_50082,RMVar_hsa_circ_335446 23189 RMVar_ID_23189 Human_SNP_ID_443127452 A-to-I Human chr10 - 95632532 95632532 95632532 TAGTGAGTCCCTGTTTCTACAAAAAATAGAAAAGTCAGCTGGACATGGTGGTATGCGCCTGCGGT TAGTGAGTCCCTGTTTCTACAAAAAATAGAAACGTCAGCTGGACATGGTGGTATGCGCCTGCGGT T G ALDH18A1 Ensembl:ENSG00000059573 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1487139209 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14907,RMVar_hsa_circ_269363,RMVar_hsa_circ_17352,RMVar_hsa_circ_55430,RMVar_hsa_circ_55685,RMVar_hsa_circ_50082,RMVar_hsa_circ_335446 23190 RMVar_ID_23190 Human_SNP_ID_443127454 A-to-I Human chr10 - 95632537 95632537 95632537 TAATATAGTGAGTCCCTGTTTCTACAAAAAATAGAAAAGTCAGCTGGACATGGTGGTATGCGCCT TAATATAGTGAGTCCCTGTTTCTACAAAAAATTGAAAAGTCAGCTGGACATGGTGGTATGCGCCT T A ALDH18A1 Ensembl:ENSG00000059573 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs976172087 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14907,RMVar_hsa_circ_269363,RMVar_hsa_circ_17352,RMVar_hsa_circ_55430,RMVar_hsa_circ_55685,RMVar_hsa_circ_50082,RMVar_hsa_circ_335446 23191 RMVar_ID_23191 Human_SNP_ID_443128852 A-to-I Human chr10 - 95638413 95638413 95638413 TTTTTGCCATTACTGTCAATGGTAAAACTGCAATTACTTTTGCACCAACCTAATACAGTCAAGTC TTTTTGCCATTACTGTCAATGGTAAAACTGCAGTTACTTTTGCACCAACCTAATACAGTCAAGTC T C ALDH18A1 Ensembl:ENSG00000059573 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1032844168 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14907,RMVar_hsa_circ_269363,RMVar_hsa_circ_50082,RMVar_hsa_circ_335446,RMVar_hsa_circ_319343,RMVar_hsa_circ_145271,RMVar_hsa_circ_145274,RMVar_hsa_circ_282091,RMVar_hsa_circ_322043,RMVar_hsa_circ_145273 23192 RMVar_ID_23192 Human_SNP_ID_443129831 A-to-I Human chr10 - 95642533 95642533 95642533 ATGGCTCACTGCAGCCTGGACCTATCGAGCTCAAGTGATACTCCCACCTCAGCCTCCCGAGTAGC ATGGCTCACTGCAGCCTGGACCTATCGAGCTCGAGTGATACTCCCACCTCAGCCTCCCGAGTAGC T C ALDH18A1 Ensembl:ENSG00000059573 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1371630163 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14907,RMVar_hsa_circ_269363,RMVar_hsa_circ_50082,RMVar_hsa_circ_335446,RMVar_hsa_circ_319343,RMVar_hsa_circ_145271,RMVar_hsa_circ_145274,RMVar_hsa_circ_282091,RMVar_hsa_circ_322043,RMVar_hsa_circ_145273 23193 RMVar_ID_23193 Human_SNP_ID_443135997 A-to-I Human chr10 - 95669939 95669939 95669939 CCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCCGCCACCTCGCCCGGCTAATTTTTTG CCTGCCTCAGCCTCCCGAGTAGCTGGGACTACGGGCGCCCGCCACCTCGCCCGGCTAATTTTTTG T C TCTN3 Ensembl:ENSG00000119977 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs573650133 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98904,RMVar_hsa_circ_122974,RMVar_hsa_circ_145275,RMVar_hsa_circ_145276 23194 RMVar_ID_23194 Human_SNP_ID_443139078 A-to-I Human chr10 - 95682450 95682450 95682450 TCACTGTGTTGCCCTGGCTCGAGTGTGGTGGCATGATCTCGGTTCACTGCAACCTCCACCCCCCG TCACTGTGTTGCCCTGGCTCGAGTGTGGTGGCTTGATCTCGGTTCACTGCAACCTCCACCCCCCG T A TCTN3 Ensembl:ENSG00000119977 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1259174168 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15716,RMVar_hsa_circ_98904,RMVar_hsa_circ_107647,RMVar_hsa_circ_145276,RMVar_hsa_circ_113043,RMVar_hsa_circ_88789,RMVar_hsa_circ_145277,RMVar_hsa_circ_145279,RMVar_hsa_circ_8549,RMVar_hsa_circ_145278 23195 RMVar_ID_23195 Human_SNP_ID_443140534 A-to-I Human chr10 - 95688132 95688132 95688132 CACCTGCCTCGGCCTCCCAAAGTGCTGGGATTATAGGCCTGAGCCACCATGCCTGGCTGAGCTTC CACCTGCCTCGGCCTCCCAAAGTGCTGGGATTGTAGGCCTGAGCCACCATGCCTGGCTGAGCTTC T C TCTN3 Ensembl:ENSG00000119977 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1166201235 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_385956,Human_RBP_ID_8342570 RMVar_hsa_circ_113043,RMVar_hsa_circ_88789,RMVar_hsa_circ_145279,RMVar_hsa_circ_145278,RMVar_hsa_circ_121708,RMVar_hsa_circ_145281,RMVar_hsa_circ_79480,RMVar_hsa_circ_145280 23196 RMVar_ID_23196 Human_SNP_ID_443141011 A-to-I Human chr10 - 95690166 95690166 95690166 CAATCCTGGCAACATAGCAAGACCCAGTCTTTACAAAAAATAGGAAAATTAGCTGGGTGTGGTGG CAATCCTGGCAACATAGCAAGACCCAGTCTTTCCAAAAAATAGGAAAATTAGCTGGGTGTGGTGG T G TCTN3 Ensembl:ENSG00000119977 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1045203491 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113043,RMVar_hsa_circ_88789,RMVar_hsa_circ_145279,RMVar_hsa_circ_145278,RMVar_hsa_circ_121708,RMVar_hsa_circ_145281,RMVar_hsa_circ_79480,RMVar_hsa_circ_145280 23197 RMVar_ID_23197 Human_SNP_ID_443141261 A-to-I Human chr10 - 95691304 95691304 95691304 ACTAAAAAAACAAAAAATTATCCAGGCATGGTAGTGGGCACCTGTAATCTCAGCTAGTTGGGAGG ACTAAAAAAACAAAAAATTATCCAGGCATGGTGGTGGGCACCTGTAATCTCAGCTAGTTGGGAGG T C TCTN3 Ensembl:ENSG00000119977 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1308798789 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113043,RMVar_hsa_circ_88789,RMVar_hsa_circ_145279,RMVar_hsa_circ_145278,RMVar_hsa_circ_121708,RMVar_hsa_circ_145281,RMVar_hsa_circ_79480,RMVar_hsa_circ_145280 23198 RMVar_ID_23198 Human_SNP_ID_443141480 A-to-I Human chr10 - 95692394 95692394 95692394 TAAAGTGATTCTCCTGCCTTAGCTTCCCGAGTAGCTGGGACTATGGGTGTGTGCCACCATGACCA TAAAGTGATTCTCCTGCCTTAGCTTCCCGAGTGGCTGGGACTATGGGTGTGTGCCACCATGACCA T C TCTN3 Ensembl:ENSG00000119977 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1241538240 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113043,RMVar_hsa_circ_88789,RMVar_hsa_circ_145279,RMVar_hsa_circ_145278,RMVar_hsa_circ_121708,RMVar_hsa_circ_145281,RMVar_hsa_circ_79480,RMVar_hsa_circ_145280 23199 RMVar_ID_23199 Human_SNP_ID_443186473 A-to-I Human chr10 - 95897620 95897620 95897620 GGAGTGTAATGGTGCGATCTCGGCTCACTGCAAGCTCCGCCTCCCGGGTTCATGCCATTCTCCTG GGAGTGTAATGGTGCGATCTCGGCTCACTGCAGGCTCCGCCTCCCGGGTTCATGCCATTCTCCTG T C ENTPD1-AS1 Ensembl:ENSG00000226688 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917637082 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8245094 Human_Splice_Rec_1163644,Human_Splice_Rec_1163645,Human_Splice_Rec_1163656,Human_Splice_Rec_1163657,Human_Splice_Rec_1163666,Human_Splice_Rec_1163667,Human_Splice_Rec_1163686,Human_Splice_Rec_1163687 RMVar_hsa_circ_97968,RMVar_hsa_circ_145286,RMVar_hsa_circ_362267,RMVar_hsa_circ_145290 23200 RMVar_ID_23200 Human_SNP_ID_443186480 A-to-I Human chr10 - 95897644 95897644 95897644 GAGTCTCGCACTGTCGCCCCAGTTGGAGTGTAATGGTGCGATCTCGGCTCACTGCAAGCTCCGCC GAGTCTCGCACTGTCGCCCCAGTTGGAGTGTAGTGGTGCGATCTCGGCTCACTGCAAGCTCCGCC T C ENTPD1-AS1 Ensembl:ENSG00000226688 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049247710 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6025420,Human_RBP_ID_8245094 Human_Splice_Rec_1163644,Human_Splice_Rec_1163645,Human_Splice_Rec_1163656,Human_Splice_Rec_1163657,Human_Splice_Rec_1163666,Human_Splice_Rec_1163667,Human_Splice_Rec_1163686,Human_Splice_Rec_1163687 RMVar_hsa_circ_97968,RMVar_hsa_circ_145286,RMVar_hsa_circ_362267,RMVar_hsa_circ_145290 23201 RMVar_ID_23201 Human_SNP_ID_443222153 A-to-I Human chr10 - 96062880 96062880 96062880 ATTGTAAAAATGAGCCAGGCATGTGGTGGTGTATGCCTACGATCCTAGCTACTCAGGAGGCTGAA ATTGTAAAAATGAGCCAGGCATGTGGTGGTGTTTGCCTACGATCCTAGCTACTCAGGAGGCTGAA T A ENTPD1-AS1 Ensembl:ENSG00000226688 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1487770331 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24850236 RMVar_hsa_circ_97968,RMVar_hsa_circ_145286 23202 RMVar_ID_23202 Human_SNP_ID_443240527 A-to-I Human chr10 + 96140732 96140732 96140732 GTAGGCAAATTGCTTGAGACCAGGAGGTCAAGACCAACCTGGGCAACATGGTGAAACCCCATCTC GTAGGCAAATTGCTTGAGACCAGGAGGTCAAGGCCAACCTGGGCAACATGGTGAAACCCCATCTC A G ZNF518A Ensembl:ENSG00000177853 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1554876207 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_329958,RMVar_hsa_circ_145300,RMVar_hsa_circ_359927,RMVar_hsa_circ_308956,RMVar_hsa_circ_145301,RMVar_hsa_circ_145302,RMVar_hsa_circ_23364 23203 RMVar_ID_23203 Human_SNP_ID_443240528 A-to-I Human chr10 + 96140735 96140733 96140736 GGCAAATTGCTTGAGACCAGGAGGTCAAGACCAACCTGGGCAACATGGTGAAACCCCATCTCTTA GGCAAATTGCTTGAGACCAGGAGGTCAAGAC___CCTGGGCAACATGGTGAAACCCCATCTCTTA CCAA C ZNF518A Ensembl:ENSG00000177853 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1416970266 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_329958,RMVar_hsa_circ_145300,RMVar_hsa_circ_359927,RMVar_hsa_circ_308956,RMVar_hsa_circ_145301,RMVar_hsa_circ_145302,RMVar_hsa_circ_23364 23204 RMVar_ID_23204 Human_SNP_ID_443261409 A-to-I Human chr10 - 96226669 96226669 96226669 GCCTGGCTAACTTTTGTATTTTTAGTAGAGACAGGATTTCCTCATGTTGGCCAGGCTGGTCTCAA GCCTGGCTAACTTTTGTATTTTTAGTAGAGACTGGATTTCCTCATGTTGGCCAGGCTGGTCTCAA T A BLNK Ensembl:ENSG00000095585 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1033205418 Functional Loss SNV dbSNP153 33..33 33 - - - 23205 RMVar_ID_23205 Human_SNP_ID_443261426 A-to-I Human chr10 - 96226719 96226719 96226719 CTCCTGCCTCAGCCTCCCGAGTAGCTGGGTCCACAGGCACCCACCACCACGCCTGGCTAACTTTT CTCCTGCCTCAGCCTCCCGAGTAGCTGGGTCCGCAGGCACCCACCACCACGCCTGGCTAACTTTT T C BLNK Ensembl:ENSG00000095585 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1245533808 Functional Loss SNV dbSNP153 33..33 33 - - - 23206 RMVar_ID_23206 Human_SNP_ID_443262800 A-to-I Human chr10 - 96232116 96232116 96232116 CTGCTTGATTCCTACACAGCAGAGTGAATCCCATTTAACCTCTAAGGTCAGTTTATGTGATAGGC CTGCTTGATTCCTACACAGCAGAGTGAATCCCTTTTAACCTCTAAGGTCAGTTTATGTGATAGGC T A BLNK Ensembl:ENSG00000095585 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1892189 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_52309 23207 RMVar_ID_23207 Human_SNP_ID_443262801 A-to-I Human chr10 - 96232116 96232116 96232116 CTGCTTGATTCCTACACAGCAGAGTGAATCCCATTTAACCTCTAAGGTCAGTTTATGTGATAGGC CTGCTTGATTCCTACACAGCAGAGTGAATCCCGTTTAACCTCTAAGGTCAGTTTATGTGATAGGC T C BLNK Ensembl:ENSG00000095585 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1892189 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_52309 23208 RMVar_ID_23208 Human_SNP_ID_443407186 A-to-I Human chr10 + 96835375 96835375 96835375 TCCACTTTAAAGATAGTAAAGTTCAGAAGATTATAGAGTCCAGAGTGCAGAGCAATATTTTAATC TCCACTTTAAAGATAGTAAAGTTCAGAAGATTGTAGAGTCCAGAGTGCAGAGCAATATTTTAATC A G LCOR Ensembl:ENSG00000196233 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025061850 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6022410,Human_RBP_ID_11478346 RMVar_hsa_circ_18638,RMVar_hsa_circ_116413,RMVar_hsa_circ_18727,RMVar_hsa_circ_145348 23209 RMVar_ID_23209 Human_SNP_ID_443410175 A-to-I Human chr10 + 96845978 96845978 96845978 CCTGTAATACCAGCACTTTGGGAGACCAAGGCAGGCAGATTATTTGAGGTCAGGAGTTTGAGACC CCTGTAATACCAGCACTTTGGGAGACCAAGGCCGGCAGATTATTTGAGGTCAGGAGTTTGAGACC A C LCOR Ensembl:ENSG00000196233 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1008945508 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18638,RMVar_hsa_circ_116413,RMVar_hsa_circ_18727,RMVar_hsa_circ_145348 23210 RMVar_ID_23210 Human_SNP_ID_443410206 A-to-I Human chr10 + 96846086 96846086 96846086 AAAACTAGCTGGGCATGGTGGTGTACAGCTGTAATCTTGGCTACTCGGGAGGCTGAGGCAGGAGA AAAACTAGCTGGGCATGGTGGTGTACAGCTGTCATCTTGGCTACTCGGGAGGCTGAGGCAGGAGA A C LCOR Ensembl:ENSG00000196233 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1370569078 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18638,RMVar_hsa_circ_116413,RMVar_hsa_circ_18727,RMVar_hsa_circ_145348 23211 RMVar_ID_23211 Human_SNP_ID_443411371 A-to-I Human chr10 + 96850294 96850294 96850294 GATCAAGGCCGGGCGCAGTGGCTCACGCCTGTAATCTTCGCACTTTGGGAGGCTGAGGTGGGAGG GATCAAGGCCGGGCGCAGTGGCTCACGCCTGTTATCTTCGCACTTTGGGAGGCTGAGGTGGGAGG A T LCOR Ensembl:ENSG00000196233 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1407519211 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24851105 RMVar_hsa_circ_18638,RMVar_hsa_circ_116413,RMVar_hsa_circ_18727,RMVar_hsa_circ_145348 23212 RMVar_ID_23212 Human_SNP_ID_443415750 A-to-I Human chr10 + 96867490 96867490 96867490 GTGGTGGCATGTACCAATAGTCCCAGCTACTCAGAAGACTGAGGTGGGAGGATCGCTTGAGCTGA GTGGTGGCATGTACCAATAGTCCCAGCTACTCTGAAGACTGAGGTGGGAGGATCGCTTGAGCTGA A T LCOR Ensembl:ENSG00000196233 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985815574 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18638,RMVar_hsa_circ_116413,RMVar_hsa_circ_18727,RMVar_hsa_circ_145351,RMVar_hsa_circ_145349,RMVar_hsa_circ_145348,RMVar_hsa_circ_84506,RMVar_hsa_circ_145350 23213 RMVar_ID_23213 Human_SNP_ID_443421255 A-to-I Human chr10 + 96887955 96887955 96887955 CACCTGCCTCAACCTCCCAAAGTGCTGGGATTACAGGCATGAACCACCACACCTGGCCTACTTTT CACCTGCCTCAACCTCCCAAAGTGCTGGGATTGCAGGCATGAACCACCACACCTGGCCTACTTTT A G LCOR Ensembl:ENSG00000196233 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs932628536 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18638,RMVar_hsa_circ_116413,RMVar_hsa_circ_18727,RMVar_hsa_circ_145351,RMVar_hsa_circ_145349,RMVar_hsa_circ_145348,RMVar_hsa_circ_84506,RMVar_hsa_circ_145352,RMVar_hsa_circ_145350 23214 RMVar_ID_23214 Human_SNP_ID_443422793 A-to-I Human chr10 + 96893712 96893712 96893712 TTGAACCCTGGAGGTGGAGGTTGCAGTAAGCCAAGATCGCGCCACTACACTCCAGCCTGGGTGAC TTGAACCCTGGAGGTGGAGGTTGCAGTAAGCCGAGATCGCGCCACTACACTCCAGCCTGGGTGAC A G LCOR Ensembl:ENSG00000196233 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1287241896 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24851281 RMVar_hsa_circ_18638,RMVar_hsa_circ_116413,RMVar_hsa_circ_18727,RMVar_hsa_circ_145351,RMVar_hsa_circ_145349,RMVar_hsa_circ_145348,RMVar_hsa_circ_84506,RMVar_hsa_circ_145352,RMVar_hsa_circ_145350 23215 RMVar_ID_23215 Human_SNP_ID_443427882 A-to-I Human chr10 + 96913777 96913777 96913777 AACCCCATCTCTACTGAAAATACAAAAATTTTAGCTGACTGTGGTGGCCCATGCCTGTAATTCCA AACCCCATCTCTACTGAAAATACAAAAATTTTGGCTGACTGTGGTGGCCCATGCCTGTAATTCCA A G LCOR Ensembl:ENSG00000196233 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005610839 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11480053 RMVar_hsa_circ_18638,RMVar_hsa_circ_116413,RMVar_hsa_circ_81972,RMVar_hsa_circ_145351,RMVar_hsa_circ_145348,RMVar_hsa_circ_361295,RMVar_hsa_circ_299619,RMVar_hsa_circ_271138,RMVar_hsa_circ_145354,RMVar_hsa_circ_145356,RMVar_hsa_circ_145357,RMVar_hsa_circ_145355,RMVar_hsa_circ_145359,RMVar_hsa_circ_125198,RMVar_hsa_circ_339156 23216 RMVar_ID_23216 Human_SNP_ID_443540942 A-to-I Human chr10 - 97364560 97364560 97364560 GGCGTGCGCCACCATGCCCAGCTAATTTTTGTATTTTTAGTAGTGATGGGGTTTTGCCATGTTGC GGCGTGCGCCACCATGCCCAGCTAATTTTTGTTTTTTTAGTAGTGATGGGGTTTTGCCATGTTGC T A RRP12 Ensembl:ENSG00000052749 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs974740213 Functional Loss SNV dbSNP153 33..33 33 - - - 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 23217 RMVar_ID_23217 Human_SNP_ID_443543989 A-to-I Human chr10 - 97374434 97374433 97374434 CATGTGGCTGGGTGCAGTGTTGCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGCACATGGA CATGTGGCTGGGTGCAGTGTTGCACACCTGTA_TCCCAGCACTTTGGGAGGCCGAGGCACATGGA AT A RRP12 Ensembl:ENSG00000052749 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1430398529 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_34213,RMVar_hsa_circ_99370,RMVar_hsa_circ_108764,RMVar_hsa_circ_93114,RMVar_hsa_circ_89390,RMVar_hsa_circ_100974,RMVar_hsa_circ_145386,RMVar_hsa_circ_145388,RMVar_hsa_circ_145387,RMVar_hsa_circ_145385,RMVar_hsa_circ_122412,RMVar_hsa_circ_42790,RMVar_hsa_circ_145393,RMVar_hsa_circ_145394,RMVar_hsa_circ_101945,RMVar_hsa_circ_145395 23218 RMVar_ID_23218 Human_SNP_ID_443544262 A-to-I Human chr10 - 97375350 97375350 97375350 CCTGTAATCCCAACACTCTGAGAGTCTGAGGCAGAAGGATTGTGTGAGGCCAAGAGTTCAAGAAC CCTGTAATCCCAACACTCTGAGAGTCTGAGGCGGAAGGATTGTGTGAGGCCAAGAGTTCAAGAAC T C RRP12 Ensembl:ENSG00000052749 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042303300 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11481887 RMVar_hsa_circ_34213,RMVar_hsa_circ_99370,RMVar_hsa_circ_108764,RMVar_hsa_circ_93114,RMVar_hsa_circ_89390,RMVar_hsa_circ_100974,RMVar_hsa_circ_145386,RMVar_hsa_circ_145388,RMVar_hsa_circ_145387,RMVar_hsa_circ_145385,RMVar_hsa_circ_122412,RMVar_hsa_circ_42790,RMVar_hsa_circ_145393,RMVar_hsa_circ_145394,RMVar_hsa_circ_101945,RMVar_hsa_circ_145395 23219 RMVar_ID_23219 Human_SNP_ID_443559535 A-to-I Human chr10 + 97429127 97429126 97429128 TTTTTTTTTTTTTTTTTTTTTTTGCGTGCGACAGAGTCTCGCTCTATCGCCCAGACTGGAGTGCA TTTTTTTTTTTTTTTTTTTTTTTGCGTGCGAC__AGTCTCGCTCTATCGCCCAGACTGGAGTGCA CAG C PGAM1 Ensembl:ENSG00000171314 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1393065893 Functional Loss DEL dbSNP153 33..34 33 - - - 23220 RMVar_ID_23220 Human_SNP_ID_443559536 A-to-I Human chr10 + 97429127 97429127 97429127 TTTTTTTTTTTTTTTTTTTTTTTGCGTGCGACAGAGTCTCGCTCTATCGCCCAGACTGGAGTGCA TTTTTTTTTTTTTTTTTTTTTTTGCGTGCGACCGAGTCTCGCTCTATCGCCCAGACTGGAGTGCA A C PGAM1 Ensembl:ENSG00000171314 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs531059672 Functional Loss SNV dbSNP153 33..33 33 - - - 23221 RMVar_ID_23221 Human_SNP_ID_443559537 A-to-I Human chr10 + 97429127 97429127 97429127 TTTTTTTTTTTTTTTTTTTTTTTGCGTGCGACAGAGTCTCGCTCTATCGCCCAGACTGGAGTGCA TTTTTTTTTTTTTTTTTTTTTTTGCGTGCGACGGAGTCTCGCTCTATCGCCCAGACTGGAGTGCA A G PGAM1 Ensembl:ENSG00000171314 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs531059672 Functional Loss SNV dbSNP153 33..33 33 - - - 23222 RMVar_ID_23222 Human_SNP_ID_443559769 A-to-I Human chr10 + 97430001 97430001 97430001 CCGGGAGGCGGAGGTTGCAGTGAGCCGAGACCACGCCACTGCACTCCAGCCTGGGTGACAGTGAG CCGGGAGGCGGAGGTTGCAGTGAGCCGAGACCGCGCCACTGCACTCCAGCCTGGGTGACAGTGAG A G PGAM1 Ensembl:ENSG00000171314 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1200565693 Functional Loss SNV dbSNP153 33..33 33 - - - 23223 RMVar_ID_23223 Human_SNP_ID_443561143 A-to-I Human chr10 - 97434819 97434819 97434819 CAGGATGGAGTGCAGTGGTGCAGTCATAGCTCACTGTAGCCTCAAACTCCTGGGCTCAGGTGATT CAGGATGGAGTGCAGTGGTGCAGTCATAGCTCCCTGTAGCCTCAAACTCCTGGGCTCAGGTGATT T G L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1426817298 Functional Loss SNV dbSNP153 33..33 33 - - - 23224 RMVar_ID_23224 Human_SNP_ID_443564562 A-to-I Human chr10 + 97447735 97447735 97447735 CCTGAGGTCGGGAGTTTGAGACCAGCCTGACCAACATGGAGAAACCCGGTCTCTACTAAAAAAAT CCTGAGGTCGGGAGTTTGAGACCAGCCTGACCGACATGGAGAAACCCGGTCTCTACTAAAAAAAT A G ZDHHC16 Ensembl:ENSG00000171307 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs909500679 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85037,RMVar_hsa_circ_145418 23225 RMVar_ID_23225 Human_SNP_ID_443564585 A-to-I Human chr10 + 97447808 97447808 97447808 AGCCAGGCGTGGTGGCACATGCCTGGAATCCCAGCCACTCAGGAGGCTGAGGCAGGAGAATTGCT AGCCAGGCGTGGTGGCACATGCCTGGAATCCCGGCCACTCAGGAGGCTGAGGCAGGAGAATTGCT A G ZDHHC16 Ensembl:ENSG00000171307 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs866716283 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85037,RMVar_hsa_circ_145418 23226 RMVar_ID_23226 Human_SNP_ID_443576559 A-to-I Human chr10 - 97492038 97492038 97492038 TGCCTCCCAGGTTCAGGTGATTCTCCTGCCTCAGCCTTCGGAGTAGCTAGGATTACAGGCATGCG TGCCTCCCAGGTTCAGGTGATTCTCCTGCCTCTGCCTTCGGAGTAGCTAGGATTACAGGCATGCG T A MMS19 Ensembl:ENSG00000155229 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971795239 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84454,RMVar_hsa_circ_145444 23227 RMVar_ID_23227 Human_SNP_ID_443576560 A-to-I Human chr10 - 97492038 97492038 97492038 TGCCTCCCAGGTTCAGGTGATTCTCCTGCCTCAGCCTTCGGAGTAGCTAGGATTACAGGCATGCG TGCCTCCCAGGTTCAGGTGATTCTCCTGCCTCGGCCTTCGGAGTAGCTAGGATTACAGGCATGCG T C MMS19 Ensembl:ENSG00000155229 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971795239 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84454,RMVar_hsa_circ_145444 23228 RMVar_ID_23228 Human_SNP_ID_443576989 A-to-I Human chr10 - 97493551 97493551 97493551 ACACTGTGATTGTTTTATTTATTTATTTTAGAAGCAGGGTCCACTCTGTTGCCCCAGCTGGAGTG ACACTGTGATTGTTTTATTTATTTATTTTAGAGGCAGGGTCCACTCTGTTGCCCCAGCTGGAGTG T C MMS19 Ensembl:ENSG00000155229 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs996993294 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84454,RMVar_hsa_circ_145444 23229 RMVar_ID_23229 Human_SNP_ID_443605030 A-to-I Human chr10 + 97604720 97604720 97604720 AAAGCTGCCATGGGAAGGGAGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGC AAAGCTGCCATGGGAAGGGAGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGC A G HOGA1,AL355315.1 Ensembl:ENSG00000241935,Ensembl:ENSG00000249967 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1415182298 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118789,RMVar_hsa_circ_145453 23230 RMVar_ID_23230 Human_SNP_ID_443605158 A-to-I Human chr10 + 97605199 97605198 97605199 GGGAGGCTGAGGGGGGTCGAATGCTTGAGCCCAGGAGTTCAAGACCAGCCTGCGCAACATGGGGA GGGAGGCTGAGGGGGGTCGAATGCTTGAGCCC_GGAGTTCAAGACCAGCCTGCGCAACATGGGGA CA C HOGA1,AL355315.1 Ensembl:ENSG00000241935,Ensembl:ENSG00000249967 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs951187893 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_118789,RMVar_hsa_circ_145453 23231 RMVar_ID_23231 Human_SNP_ID_443605192 A-to-I Human chr10 + 97605331 97605331 97605331 TGGGAGGCTGAGGCAGAAGGGAAGATCCCTTGAATCTGGGAGGTTGAGGCTGCAGTGAGCTGTGA TGGGAGGCTGAGGCAGAAGGGAAGATCCCTTGGATCTGGGAGGTTGAGGCTGCAGTGAGCTGTGA A G HOGA1,AL355315.1 Ensembl:ENSG00000241935,Ensembl:ENSG00000249967 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs906775564 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118789,RMVar_hsa_circ_145453 23232 RMVar_ID_23232 Human_SNP_ID_443609374 A-to-I Human chr10 - 97622587 97622587 97622587 GGGTTCAAGCGATCCTTCCACCTCAGCCTCCCAAGTAGCTGGGACTACAGGAACGCACCACCACA GGGTTCAAGCGATCCTTCCACCTCAGCCTCCCGAGTAGCTGGGACTACAGGAACGCACCACCACA T C MORN4 Ensembl:ENSG00000171160 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1252482447 Functional Loss SNV dbSNP153 33..33 33 - - - 23233 RMVar_ID_23233 Human_SNP_ID_443616542 A-to-I Human chr10 + 97650456 97650456 97650456 GGTGTGCACCACCGCGCCCAGCTACTTTTTGTATTTTTAGTAGAGACAGGGTTTCGCCATGTTGG GGTGTGCACCACCGCGCCCAGCTACTTTTTGTGTTTTTAGTAGAGACAGGGTTTCGCCATGTTGG A G PI4K2A,AL355315.1 Ensembl:ENSG00000155252,Ensembl:ENSG00000249967 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1022295520 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118789,RMVar_hsa_circ_145453 23234 RMVar_ID_23234 Human_SNP_ID_443618149 A-to-I Human chr10 + 97658093 97658093 97658093 ACCTCAGGTGATCCACCCATCTCAGTGTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCATGC ACCTCAGGTGATCCACCCATCTCAGTGTCCCAGAGTGCTGGGATTACAGGTGTGAGCCACCATGC A G PI4K2A,AL355315.1 Ensembl:ENSG00000155252,Ensembl:ENSG00000249967 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs998202657 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_145457,RMVar_hsa_circ_285412,RMVar_hsa_circ_319046,RMVar_hsa_circ_341348,RMVar_hsa_circ_292506,RMVar_hsa_circ_145459,RMVar_hsa_circ_145458 23235 RMVar_ID_23235 Human_SNP_ID_443621365 A-to-I Human chr10 + 97672315 97672315 97672315 TGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGACATGAGCCACTACGCCCGGACCAAAACC TGCCCACCTCGGCCTCCCAAAGTGCTGGGATTGCAGACATGAGCCACTACGCCCGGACCAAAACC A G PI4K2A,AL355315.1 Ensembl:ENSG00000155252,Ensembl:ENSG00000249967 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs993778349 Functional Loss SNV dbSNP153 33..33 33 - - - 23236 RMVar_ID_23236 Human_SNP_ID_443669983 A-to-I Human chr10 + 97867877 97867877 97867877 CATGGGGAGCAGGATGAACTCTGTCTTCTTGGAGCTTGCAGTCTACTGAAGAGGCAGACACCTCA CATGGGGAGCAGGATGAACTCTGTCTTCTTGGGGCTTGCAGTCTACTGAAGAGGCAGACACCTCA A G GOLGA7B Ensembl:ENSG00000155265 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs532389847 Functional Loss SNV dbSNP153 33..33 33 - - - 23237 RMVar_ID_23237 Human_SNP_ID_443759529 A-to-I Human chr10 + 98239910 98239910 98239910 TAGTGATGGGGTCTCTCTGTGTTGCCTAGGCTAGTCTCAAACTCTTGGACTCAAGTGATCTCCTG TAGTGATGGGGTCTCTCTGTGTTGCCTAGGCTGGTCTCAAACTCTTGGACTCAAGTGATCTCCTG A G R3HCC1L Ensembl:ENSG00000166024 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1365134438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8343207 RMVar_hsa_circ_145480,RMVar_hsa_circ_127047 23238 RMVar_ID_23238 Human_SNP_ID_443800230 A-to-I Human chr10 - 98398918 98398918 98398918 TTGCCCAGGCTGGTCTGGAACTCTTGAGCTCAAGCAATCCTCCCACCTCCACCTCCCAAGGTGCT TTGCCCAGGCTGGTCTGGAACTCTTGAGCTCAGGCAATCCTCCCACCTCCACCTCCCAAGGTGCT T C PYROXD2 Ensembl:ENSG00000119943 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1419997656 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92905,RMVar_hsa_circ_145491,RMVar_hsa_circ_37996,RMVar_hsa_circ_76449,RMVar_hsa_circ_321680,RMVar_hsa_circ_145495,RMVar_hsa_circ_145496 23239 RMVar_ID_23239 Human_SNP_ID_443942755 A-to-I Human chr10 - 99013280 99013280 99013280 TTAGCACATGAGGACCTAAGAAAAGCTGGGTTACTGATTTTTGCTAATAAACAAGATGTTAAAAA TTAGCACATGAGGACCTAAGAAAAGCTGGGTTGCTGATTTTTGCTAATAAACAAGATGTTAAAAA T C HPSE2,ARL5AP2 Ensembl:ENSG00000172987,Ensembl:ENSG00000236818 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs576931798 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_378286 23240 RMVar_ID_23240 Human_SNP_ID_443942759 A-to-I Human chr10 - 99013307 99013307 99013307 TCTGTAACTAGAGAACTCTATAAAATGTTAGCACATGAGGACCTAAGAAAAGCTGGGTTACTGAT TCTGTAACTAGAGAACTCTATAAAATGTTAGCGCATGAGGACCTAAGAAAAGCTGGGTTACTGAT T C HPSE2,ARL5AP2 Ensembl:ENSG00000172987,Ensembl:ENSG00000236818 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1362869634 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_378286 23241 RMVar_ID_23241 Human_SNP_ID_444108959 A-to-I Human chr10 - 99713906 99713906 99713906 AGTACAATGGCGTGATCTCAGCTCACTCTGCAACCTCCACTTCCCAGGTTCAAGCGATTCTCATG AGTACAATGGCGTGATCTCAGCTCACTCTGCAGCCTCCACTTCCCAGGTTCAAGCGATTCTCATG T C COX15,AL133353.2 Ensembl:ENSG00000014919,Ensembl:ENSG00000285932 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924884270 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_367454,Human_RBP_ID_5914748,Human_RBP_ID_8756520,Human_RBP_ID_11227457,Human_RBP_ID_17225023,Human_RBP_ID_17341822,Human_RBP_ID_17457119,Human_RBP_ID_27403018 23242 RMVar_ID_23242 Human_SNP_ID_444108965 A-to-I Human chr10 - 99713935 99713935 99713935 CAGAGTTTCACTCTTGTTGCCCAGGCTGGAGTACAATGGCGTGATCTCAGCTCACTCTGCAACCT CAGAGTTTCACTCTTGTTGCCCAGGCTGGAGTGCAATGGCGTGATCTCAGCTCACTCTGCAACCT T C COX15,AL133353.2 Ensembl:ENSG00000014919,Ensembl:ENSG00000285932 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs994920269 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18236618,Human_RBP_ID_26391430 23243 RMVar_ID_23243 Human_SNP_ID_444109859 A-to-I Human chr10 - 99717598 99717598 99717598 GGATTGTTTGAGCAGGAGTTTGAGGCTGCAGTAAGCTGTGATCACGTTACTGCATTCTAGCCTGG GGATTGTTTGAGCAGGAGTTTGAGGCTGCAGTGAGCTGTGATCACGTTACTGCATTCTAGCCTGG T C COX15,AL133353.2 Ensembl:ENSG00000014919,Ensembl:ENSG00000285932 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1040336556 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12544,RMVar_hsa_circ_352232 23244 RMVar_ID_23244 Human_SNP_ID_444110489 A-to-I Human chr10 - 99720442 99720442 99720442 CAACACAGGATTTTTTCATTCTTTTTTTTGAGACTGAGTCTCACTCTGTTGCCCAGGCTGGAGTG CAACACAGGATTTTTTCATTCTTTTTTTTGAGTCTGAGTCTCACTCTGTTGCCCAGGCTGGAGTG T A COX15,AL133353.2 Ensembl:ENSG00000014919,Ensembl:ENSG00000285932 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749469766 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8323413 RMVar_hsa_circ_12544,RMVar_hsa_circ_352232,RMVar_hsa_circ_31322 23245 RMVar_ID_23245 Human_SNP_ID_444114179 A-to-I Human chr10 + 99735688 99735688 99735688 CCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCATCACACCCGGCCAGATAACTAATAC CCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCATCACACCCGGCCAGATAACTAATAC A G CUTC Ensembl:ENSG00000119929 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7917770 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101680,RMVar_hsa_circ_145520 23246 RMVar_ID_23246 Human_SNP_ID_444116480 A-to-I Human chr10 + 99745601 99745601 99745601 TAGGATGGGGCTGGGCACAGTGGCTTACCCCTATAATCCTACCACTTTGGGAGACCGAGGTGGGT TAGGATGGGGCTGGGCACAGTGGCTTACCCCTGTAATCCTACCACTTTGGGAGACCGAGGTGGGT A G CUTC Ensembl:ENSG00000119929 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1249158406 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24771728 RMVar_hsa_circ_20354,RMVar_hsa_circ_101680,RMVar_hsa_circ_348736,RMVar_hsa_circ_145520,RMVar_hsa_circ_78059,RMVar_hsa_circ_81868,RMVar_hsa_circ_145521,RMVar_hsa_circ_145522 23247 RMVar_ID_23247 Human_SNP_ID_444127597 A-to-I Human chr10 + 99794662 99794661 99794662 CACCTCCTGGGTTCAAGTGATTATCCTGCCTCAGCCTCGCAAGTAGCTGGGATTACAGGTGTGAG CACCTCCTGGGTTCAAGTGATTATCCTGCCTC_GCCTCGCAAGTAGCTGGGATTACAGGTGTGAG CA C ABCC2 Ensembl:ENSG00000023839 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1357093491 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_112634,RMVar_hsa_circ_118260,RMVar_hsa_circ_11062,RMVar_hsa_circ_107979,RMVar_hsa_circ_145525,RMVar_hsa_circ_145526,RMVar_hsa_circ_127932,RMVar_hsa_circ_95581,RMVar_hsa_circ_84578,RMVar_hsa_circ_145528,RMVar_hsa_circ_145529,RMVar_hsa_circ_145527,RMVar_hsa_circ_145532,RMVar_hsa_circ_95147,RMVar_hsa_circ_58476,RMVar_hsa_circ_114491,RMVar_hsa_circ_124552,RMVar_hsa_circ_145533,RMVar_hsa_circ_115800,RMVar_hsa_circ_110300,RMVar_hsa_circ_79121,RMVar_hsa_circ_145537,RMVar_hsa_circ_145539,RMVar_hsa_circ_145540,RMVar_hsa_circ_145538,RMVar_hsa_circ_145536,RMVar_hsa_circ_145541,RMVar_hsa_circ_113090 23248 RMVar_ID_23248 Human_SNP_ID_444127819 A-to-I Human chr10 + 99795607 99795607 99795607 TGTAATCCCAGCTCCTTGGGAGGCTGAGACAGAAGAATTGCTTGAACCTGGGAGGCAGAGGTTGC TGTAATCCCAGCTCCTTGGGAGGCTGAGACAGGAGAATTGCTTGAACCTGGGAGGCAGAGGTTGC A G ABCC2 Ensembl:ENSG00000023839 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1254718827 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112634,RMVar_hsa_circ_118260,RMVar_hsa_circ_11062,RMVar_hsa_circ_107979,RMVar_hsa_circ_145525,RMVar_hsa_circ_145526,RMVar_hsa_circ_127932,RMVar_hsa_circ_95581,RMVar_hsa_circ_84578,RMVar_hsa_circ_145528,RMVar_hsa_circ_145529,RMVar_hsa_circ_145527,RMVar_hsa_circ_145532,RMVar_hsa_circ_95147,RMVar_hsa_circ_58476,RMVar_hsa_circ_114491,RMVar_hsa_circ_124552,RMVar_hsa_circ_145533,RMVar_hsa_circ_115800,RMVar_hsa_circ_110300,RMVar_hsa_circ_79121,RMVar_hsa_circ_145537,RMVar_hsa_circ_145539,RMVar_hsa_circ_145540,RMVar_hsa_circ_145538,RMVar_hsa_circ_145536,RMVar_hsa_circ_145541,RMVar_hsa_circ_113090 23249 RMVar_ID_23249 Human_SNP_ID_444156364 A-to-I Human chr10 - 99902116 99902115 99902117 AAGGGCCGAGGCAGGTGGATCACTTGAGCCCAAGAGTTTGTGACCAGCCTGACCAACGTGCCGAA AAGGGCCGAGGCAGGTGGATCACTTGAGCCC__GAGTTTGTGACCAGCCTGACCAACGTGCCGAA CTT C DNMBP Ensembl:ENSG00000107554 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1472757414 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_102621,RMVar_hsa_circ_145580,RMVar_hsa_circ_28419,RMVar_hsa_circ_32273,RMVar_hsa_circ_35493,RMVar_hsa_circ_46681,RMVar_hsa_circ_324573,RMVar_hsa_circ_145583,RMVar_hsa_circ_33149,RMVar_hsa_circ_325488,RMVar_hsa_circ_145588,RMVar_hsa_circ_51010 23250 RMVar_ID_23250 Human_SNP_ID_444156365 A-to-I Human chr10 - 99902116 99902116 99902116 AAGGGCCGAGGCAGGTGGATCACTTGAGCCCAAGAGTTTGTGACCAGCCTGACCAACGTGCCGAA AAGGGCCGAGGCAGGTGGATCACTTGAGCCCAGGAGTTTGTGACCAGCCTGACCAACGTGCCGAA T C DNMBP Ensembl:ENSG00000107554 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs899408831 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102621,RMVar_hsa_circ_145580,RMVar_hsa_circ_28419,RMVar_hsa_circ_32273,RMVar_hsa_circ_35493,RMVar_hsa_circ_46681,RMVar_hsa_circ_324573,RMVar_hsa_circ_145583,RMVar_hsa_circ_33149,RMVar_hsa_circ_325488,RMVar_hsa_circ_145588,RMVar_hsa_circ_51010 23251 RMVar_ID_23251 Human_SNP_ID_444156368 A-to-I Human chr10 - 99902127 99902126 99902127 CAGCACTTTGGAAGGGCCGAGGCAGGTGGATCACTTGAGCCCAAGAGTTTGTGACCAGCCTGACC CAGCACTTTGGAAGGGCCGAGGCAGGTGGATC_CTTGAGCCCAAGAGTTTGTGACCAGCCTGACC GT G DNMBP Ensembl:ENSG00000107554 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1488796651 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_102621,RMVar_hsa_circ_145580,RMVar_hsa_circ_28419,RMVar_hsa_circ_32273,RMVar_hsa_circ_35493,RMVar_hsa_circ_46681,RMVar_hsa_circ_324573,RMVar_hsa_circ_145583,RMVar_hsa_circ_33149,RMVar_hsa_circ_325488,RMVar_hsa_circ_145588,RMVar_hsa_circ_51010 23252 RMVar_ID_23252 Human_SNP_ID_444157323 A-to-I Human chr10 - 99905842 99905842 99905842 CCTCAGCTCCCTGAGCAGCTGGAACTATAGGCATGCACCATCAGGCCCAGCTAGTTTTTAAATTT CCTCAGCTCCCTGAGCAGCTGGAACTATAGGCGTGCACCATCAGGCCCAGCTAGTTTTTAAATTT T C DNMBP Ensembl:ENSG00000107554 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1352021158 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102621,RMVar_hsa_circ_145580,RMVar_hsa_circ_28419,RMVar_hsa_circ_32273,RMVar_hsa_circ_35493,RMVar_hsa_circ_46681,RMVar_hsa_circ_324573,RMVar_hsa_circ_145583,RMVar_hsa_circ_33149,RMVar_hsa_circ_325488,RMVar_hsa_circ_145588,RMVar_hsa_circ_51010 23253 RMVar_ID_23253 Human_SNP_ID_444157346 A-to-I Human chr10 - 99905956 99905956 99905956 CTGTTGTTTCTTCTTTTTTTAGACAGGGTCTCACATTGTTATCCAGACTGGACTGCAGTGGCACA CTGTTGTTTCTTCTTTTTTTAGACAGGGTCTCTCATTGTTATCCAGACTGGACTGCAGTGGCACA T A DNMBP Ensembl:ENSG00000107554 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1370163575 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2185007 RMVar_hsa_circ_102621,RMVar_hsa_circ_145580,RMVar_hsa_circ_28419,RMVar_hsa_circ_32273,RMVar_hsa_circ_35493,RMVar_hsa_circ_46681,RMVar_hsa_circ_324573,RMVar_hsa_circ_145583,RMVar_hsa_circ_33149,RMVar_hsa_circ_325488,RMVar_hsa_circ_145588,RMVar_hsa_circ_51010 23254 RMVar_ID_23254 Human_SNP_ID_444177909 A-to-I Human chr10 - 99991547 99991547 99991547 AAATGATATGAAGACCTTGAAAACATTGTACTAGGAAGCCAATCACAAAAGACCACATATTACAT AAATGATATGAAGACCTTGAAAACATTGTACTGGGAAGCCAATCACAAAAGACCACATATTACAT T C DNMBP Ensembl:ENSG00000107554 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1458752022 Functional Loss SNV dbSNP153 33..33 33 - - - 23255 RMVar_ID_23255 Human_SNP_ID_444227765 A-to-I Human chr10 - 100208378 100208378 100208378 TTCTTGGCTTGGTGCAGTGGCCCATGCCTGTAATCCCGGGACTTTGGGAACCCAAGGTGGGTGGA TTCTTGGCTTGGTGCAGTGGCCCATGCCTGTAGTCCCGGGACTTTGGGAACCCAAGGTGGGTGGA T C CHUK Ensembl:ENSG00000213341 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1020939643 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_296626,RMVar_hsa_circ_9313,RMVar_hsa_circ_145602,RMVar_hsa_circ_145603,RMVar_hsa_circ_105737,RMVar_hsa_circ_145605,RMVar_hsa_circ_15033,RMVar_hsa_circ_61133,RMVar_hsa_circ_6332,RMVar_hsa_circ_34069,RMVar_hsa_circ_78448,RMVar_hsa_circ_145607 23256 RMVar_ID_23256 Human_SNP_ID_444233424 A-to-I Human chr10 - 100232541 100232541 100232541 GGGCGTGGTGCCAGGCACTTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAG GGGCGTGGTGCCAGGCACTTGTAATCCCAGCTGCTCAGGAGGCTGAGGCAGGAGAATTGCTTGAG T C CWF19L1 Ensembl:ENSG00000095485 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1131136 Functional Loss SNV dbSNP153 33..33 33 - - - 23257 RMVar_ID_23257 Human_SNP_ID_444233427 A-to-I Human chr10 - 100232557 100232555 100232557 GCTACAAAAATTAGCTGGGCGTGGTGCCAGGCACTTGTAATCCCAGCTACTCAGGAGGCTGAGGC GCTACAAAAATTAGCTGGGCGTGGTGCCAGGC__TTGTAATCCCAGCTACTCAGGAGGCTGAGGC AGT A CWF19L1 Ensembl:ENSG00000095485 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1220020225 Functional Loss DEL dbSNP153 33..34 33 - - - Human_miRNA_ID_768808,Human_miRNA_ID_773709,Human_miRNA_ID_778535,Human_miRNA_ID_783414,Human_miRNA_ID_788248,Human_miRNA_ID_1096524,Human_miRNA_ID_1104743,Human_miRNA_ID_1109547,Human_miRNA_ID_1565731,Human_miRNA_ID_1571378,Human_miRNA_ID_1578560,Human_miRNA_ID_1597897,Human_miRNA_ID_1607344,Human_miRNA_ID_1612257,Human_miRNA_ID_1619738,Human_miRNA_ID_1635864 23258 RMVar_ID_23258 Human_SNP_ID_444233498 A-to-I Human chr10 - 100232927 100232927 100232927 GTTGCCCAGGCTGGTCTGTAATGCCTAGGCTCAAGGGATCCTCTGCCTTGGCTTCTTAACCTGCT GTTGCCCAGGCTGGTCTGTAATGCCTAGGCTCGAGGGATCCTCTGCCTTGGCTTCTTAACCTGCT T C CWF19L1 Ensembl:ENSG00000095485 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1219348470 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4101302,Human_RBP_ID_5915497,Human_RBP_ID_11229632,Human_RBP_ID_26391544 23259 RMVar_ID_23259 Human_SNP_ID_444233526 A-to-I Human chr10 - 100233026 100233026 100233026 CTCCCACCTCAGCCTCATGAGTAGCTGGGACCACAGGCGCATGCTACCATGCCTGGCAAACTTTT CTCCCACCTCAGCCTCATGAGTAGCTGGGACCGCAGGCGCATGCTACCATGCCTGGCAAACTTTT T C CWF19L1 Ensembl:ENSG00000095485 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs3190709 Functional Loss SNV dbSNP153 33..33 33 - - - 23260 RMVar_ID_23260 Human_SNP_ID_444233530 A-to-I Human chr10 - 100233048 100233048 100233048 AACCTCCTGGGCTCTAGAGTTCCTCCCACCTCAGCCTCATGAGTAGCTGGGACCACAGGCGCATG AACCTCCTGGGCTCTAGAGTTCCTCCCACCTCGGCCTCATGAGTAGCTGGGACCACAGGCGCATG T C CWF19L1 Ensembl:ENSG00000095485 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1131131 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1393935 23261 RMVar_ID_23261 Human_SNP_ID_444233535 A-to-I Human chr10 - 100233091 100233091 100233091 CAAGCAGGATTGCAGTGGCATAACTGTGGCTCACTGTAGCCTCAACCTCCTGGGCTCTAGAGTTC CAAGCAGGATTGCAGTGGCATAACTGTGGCTCTCTGTAGCCTCAACCTCCTGGGCTCTAGAGTTC T A CWF19L1 Ensembl:ENSG00000095485 Protein coding 3'UTR GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;ASD brains,cerebellum;Bronchiolar epithelium,BEP2D cell line - 29129909,30559470,31158229 RNA-Seq:(High) rs911787427 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11229640 Human_miRNA_ID_274851 23262 RMVar_ID_23262 Human_SNP_ID_444233539 A-to-I Human chr10 - 100233121 100233121 100233121 TTTTTTGAGACAAAGTCTCGCTCTGTCACCCAAGCAGGATTGCAGTGGCATAACTGTGGCTCACT TTTTTTGAGACAAAGTCTCGCTCTGTCACCCAGGCAGGATTGCAGTGGCATAACTGTGGCTCACT T C CWF19L1 Ensembl:ENSG00000095485 Protein coding 3'UTR GSE38233;GSE100210;GSE112787 cultured B-cells;HepG2 cell line;293 Flip-In T-REx cells,empty vector - 24183664,29129909,29967493 RNA-Seq:(High) rs15663 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11229642,Human_RBP_ID_23151019,Human_RBP_ID_26399251,Human_RBP_ID_26872821,Human_RBP_ID_27188452 Human_Splice_Rec_1168073 Human_miRNA_ID_1092370 23263 RMVar_ID_23263 Human_SNP_ID_444233544 A-to-I Human chr10 - 100233140 100233140 100233140 TTTTTTAATTAAAAGAATTTTTTTTGAGACAAAGTCTCGCTCTGTCACCCAAGCAGGATTGCAGT TTTTTTAATTAAAAGAATTTTTTTTGAGACAATGTCTCGCTCTGTCACCCAAGCAGGATTGCAGT T A CWF19L1 Ensembl:ENSG00000095485 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs943041078 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11229643,Human_RBP_ID_26391550,Human_RBP_ID_26872821 Human_Splice_Rec_1168073 23264 RMVar_ID_23264 Human_SNP_ID_444233545 A-to-I Human chr10 - 100233141 100233141 100233141 TTTTTTTAATTAAAAGAATTTTTTTTGAGACAAAGTCTCGCTCTGTCACCCAAGCAGGATTGCAG TTTTTTTAATTAAAAGAATTTTTTTTGAGACAGAGTCTCGCTCTGTCACCCAAGCAGGATTGCAG T C CWF19L1 Ensembl:ENSG00000095485 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1131127 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11229643,Human_RBP_ID_26391550,Human_RBP_ID_26872821 Human_Splice_Rec_1168073 23265 RMVar_ID_23265 Human_SNP_ID_444233546 A-to-I Human chr10 - 100233142 100233142 100233142 TTTTTTTTAATTAAAAGAATTTTTTTTGAGACAAAGTCTCGCTCTGTCACCCAAGCAGGATTGCA TTTTTTTTAATTAAAAGAATTTTTTTTGAGACGAAGTCTCGCTCTGTCACCCAAGCAGGATTGCA T C CWF19L1 Ensembl:ENSG00000095485 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1131126 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11229643,Human_RBP_ID_26391550,Human_RBP_ID_26872821 Human_Splice_Rec_1168073 23266 RMVar_ID_23266 Human_SNP_ID_444236952 A-to-I Human chr10 - 100247774 100247774 100247774 CTCCTGCCTCAGCCTCCTGAGTAGCTGGAACTATAGGTGTGTGCCACCATGCCTGGCTAATCTTT CTCCTGCCTCAGCCTCCTGAGTAGCTGGAACTGTAGGTGTGTGCCACCATGCCTGGCTAATCTTT T C CWF19L1 Ensembl:ENSG00000095485 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs767942800 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45876,RMVar_hsa_circ_290227,RMVar_hsa_circ_145613,RMVar_hsa_circ_145615,RMVar_hsa_circ_296478,RMVar_hsa_circ_365277,RMVar_hsa_circ_298682,RMVar_hsa_circ_340837,RMVar_hsa_circ_267828 23267 RMVar_ID_23267 Human_SNP_ID_444236957 A-to-I Human chr10 - 100247784 100247784 100247784 TCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGAACTATAGGTGTGTGCCACCATGCCTG TCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTGGCTGGAACTATAGGTGTGTGCCACCATGCCTG T C CWF19L1 Ensembl:ENSG00000095485 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1006185933 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45876,RMVar_hsa_circ_290227,RMVar_hsa_circ_145613,RMVar_hsa_circ_145615,RMVar_hsa_circ_296478,RMVar_hsa_circ_365277,RMVar_hsa_circ_298682,RMVar_hsa_circ_340837,RMVar_hsa_circ_267828 23268 RMVar_ID_23268 Human_SNP_ID_444236973 A-to-I Human chr10 - 100247833 100247833 100247833 GGAGTGTAGTGGCACGATCTCGGCTTACTGCAACCTCCACCTCCCATGTTCAAGCGATTCTCCTG GGAGTGTAGTGGCACGATCTCGGCTTACTGCATCCTCCACCTCCCATGTTCAAGCGATTCTCCTG T A CWF19L1 Ensembl:ENSG00000095485 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs187458851 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45876,RMVar_hsa_circ_290227,RMVar_hsa_circ_145613,RMVar_hsa_circ_145615,RMVar_hsa_circ_296478,RMVar_hsa_circ_365277,RMVar_hsa_circ_298682,RMVar_hsa_circ_340837,RMVar_hsa_circ_267828 23269 RMVar_ID_23269 Human_SNP_ID_444236974 A-to-I Human chr10 - 100247833 100247833 100247833 GGAGTGTAGTGGCACGATCTCGGCTTACTGCAACCTCCACCTCCCATGTTCAAGCGATTCTCCTG GGAGTGTAGTGGCACGATCTCGGCTTACTGCAGCCTCCACCTCCCATGTTCAAGCGATTCTCCTG T C CWF19L1 Ensembl:ENSG00000095485 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs187458851 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45876,RMVar_hsa_circ_290227,RMVar_hsa_circ_145613,RMVar_hsa_circ_145615,RMVar_hsa_circ_296478,RMVar_hsa_circ_365277,RMVar_hsa_circ_298682,RMVar_hsa_circ_340837,RMVar_hsa_circ_267828 23270 RMVar_ID_23270 Human_SNP_ID_444238519 A-to-I Human chr10 - 100254009 100254009 100254009 AGGTGTGGTGGCACGTGCCTGTAATCCCAGCTACTAGGGAGGCTGAGGCAGGAGAATCACTTCTT AGGTGTGGTGGCACGTGCCTGTAATCCCAGCTGCTAGGGAGGCTGAGGCAGGAGAATCACTTCTT T C CWF19L1 Ensembl:ENSG00000095485 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1189647064 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45876,RMVar_hsa_circ_365277,RMVar_hsa_circ_340837,RMVar_hsa_circ_145619,RMVar_hsa_circ_316910,RMVar_hsa_circ_267828,RMVar_hsa_circ_311122,RMVar_hsa_circ_145618 23271 RMVar_ID_23271 Human_SNP_ID_444238791 A-to-I Human chr10 - 100255293 100255293 100255293 GCTGGTCTTGAACTCCTGCGCTCTAGTGATCCACCCGCCTTGGCCTCCCAAAGTGCTGGGATTAC GCTGGTCTTGAACTCCTGCGCTCTAGTGATCCGCCCGCCTTGGCCTCCCAAAGTGCTGGGATTAC T C CWF19L1 Ensembl:ENSG00000095485 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1470488461 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11230144 RMVar_hsa_circ_45876,RMVar_hsa_circ_365277,RMVar_hsa_circ_340837,RMVar_hsa_circ_145619,RMVar_hsa_circ_316910,RMVar_hsa_circ_267828,RMVar_hsa_circ_311122,RMVar_hsa_circ_145618 23272 RMVar_ID_23272 Human_SNP_ID_444239360 A-to-I Human chr10 - 100257438 100257437 100257438 AAAATTAACTGGGCATGGTGGCGGTCACCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA AAAATTAACTGGGCATGGTGGCGGTCACCTGT_GTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA CT C CWF19L1 Ensembl:ENSG00000095485 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264006506 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_45876,RMVar_hsa_circ_145619,RMVar_hsa_circ_316910,RMVar_hsa_circ_311122,RMVar_hsa_circ_145620,RMVar_hsa_circ_369377,RMVar_hsa_circ_145618,RMVar_hsa_circ_343364 23273 RMVar_ID_23273 Human_SNP_ID_444239361 A-to-I Human chr10 - 100257438 100257438 100257438 AAAATTAACTGGGCATGGTGGCGGTCACCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA AAAATTAACTGGGCATGGTGGCGGTCACCTGTGGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA T C CWF19L1 Ensembl:ENSG00000095485 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956069613 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45876,RMVar_hsa_circ_145619,RMVar_hsa_circ_316910,RMVar_hsa_circ_311122,RMVar_hsa_circ_145620,RMVar_hsa_circ_369377,RMVar_hsa_circ_145618,RMVar_hsa_circ_343364 23274 RMVar_ID_23274 Human_SNP_ID_444241022 A-to-I Human chr10 - 100264482 100264482 100264482 GGAGTGCAGTGCCGCGATCTCAGCTCACTGCAAGCTCTGCCTCGTGGGTTCATGCTATTCTCCCG GGAGTGCAGTGCCGCGATCTCAGCTCACTGCAGGCTCTGCCTCGTGGGTTCATGCTATTCTCCCG T C CWF19L1 Ensembl:ENSG00000095485 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1247565169 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102000,RMVar_hsa_circ_145623 23275 RMVar_ID_23275 Human_SNP_ID_444241023 A-to-I Human chr10 - 100264482 100264482 100264482 GGAGTGCAGTGCCGCGATCTCAGCTCACTGCAAGCTCTGCCTCGTGGGTTCATGCTATTCTCCCG GGAGTGCAGTGCCGCGATCTCAGCTCACTGCACGCTCTGCCTCGTGGGTTCATGCTATTCTCCCG T G CWF19L1 Ensembl:ENSG00000095485 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1247565169 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102000,RMVar_hsa_circ_145623 23276 RMVar_ID_23276 Human_SNP_ID_444246812 A-to-I Human chr10 - 100284631 100284631 100284631 CAAAAATTAGCCAGGTGTGGTGGCACACGCCTATAATCCCAGCTACTCAGGAGGCTGACACGGGA CAAAAATTAGCCAGGTGTGGTGGCACACGCCTGTAATCCCAGCTACTCAGGAGGCTGACACGGGA T C BLOC1S2 Ensembl:ENSG00000196072 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs987100053 Functional Loss SNV dbSNP153 33..33 33 - - - 23277 RMVar_ID_23277 Human_SNP_ID_444246874 A-to-I Human chr10 - 100284928 100284928 100284928 AGATACATCTTAGTCTGCTTCCATCCCTCAATATCTACTTGAACAAGTCCTATAAATTCCACTTC AGATACATCTTAGTCTGCTTCCATCCCTCAATGTCTACTTGAACAAGTCCTATAAATTCCACTTC T C BLOC1S2 Ensembl:ENSG00000196072 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1316361164 Functional Loss SNV dbSNP153 33..33 33 - - - 23278 RMVar_ID_23278 Human_SNP_ID_444265402 A-to-I Human chr10 + 100358139 100358139 100358139 CTCGGGGTTCAGCCTCCCAAGTAACTGGGATTACAGGTGCATGCCACCATGCTTGGCTAATTTTT CTCGGGGTTCAGCCTCCCAAGTAACTGGGATTGCAGGTGCATGCCACCATGCTTGGCTAATTTTT A G SCD Ensembl:ENSG00000099194 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs931528540 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17559167 RMVar_hsa_circ_105925,RMVar_hsa_circ_145626,RMVar_hsa_circ_116351,RMVar_hsa_circ_145629 23279 RMVar_ID_23279 Human_SNP_ID_444265416 A-to-I Human chr10 + 100358201 100358201 100358201 TTTCTATTTTTTTGTAGAGACATGGTTTTGCCATGTTGCACAGGCTGGTCTCGAACTCCTGAGCT TTTCTATTTTTTTGTAGAGACATGGTTTTGCCGTGTTGCACAGGCTGGTCTCGAACTCCTGAGCT A G SCD Ensembl:ENSG00000099194 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1464723915 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105925,RMVar_hsa_circ_145626,RMVar_hsa_circ_116351,RMVar_hsa_circ_145629 23280 RMVar_ID_23280 Human_SNP_ID_444266313 A-to-I Human chr10 + 100361844 100361844 100361844 TGTTTCCAGAATTGGTAAAAACAGCAGCTCATAGAATTTTGAGTATTCCATGAGCTGCTCATTAC TGTTTCCAGAATTGGTAAAAACAGCAGCTCATGGAATTTTGAGTATTCCATGAGCTGCTCATTAC A G SCD Ensembl:ENSG00000099194 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs3178760 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_367764,Human_RBP_ID_980984,Human_RBP_ID_1125336,Human_RBP_ID_1156738,Human_RBP_ID_1258504,Human_RBP_ID_4101529,Human_RBP_ID_5255178,Human_RBP_ID_5915861,Human_RBP_ID_8173440,Human_RBP_ID_8245425,Human_RBP_ID_8725098,Human_RBP_ID_8756625,Human_RBP_ID_8981251,Human_RBP_ID_17182979,Human_RBP_ID_17225090,Human_RBP_ID_17341881,Human_RBP_ID_17457219,Human_RBP_ID_17667624,Human_RBP_ID_17767444,Human_RBP_ID_18236723,Human_RBP_ID_18510430,Human_RBP_ID_18525495,Human_RBP_ID_18544116,Human_RBP_ID_19452053,Human_RBP_ID_22378474,Human_RBP_ID_22414373,Human_RBP_ID_22787090,Human_RBP_ID_23151046,Human_RBP_ID_24402346,Human_RBP_ID_26391670,Human_RBP_ID_26872898,Human_RBP_ID_27601776 Human_miRNA_ID_1894789,Human_miRNA_ID_1910669,Human_miRNA_ID_2894155,Human_miRNA_ID_3097732 RMVar_hsa_circ_95357,RMVar_hsa_circ_105925,RMVar_hsa_circ_145626,RMVar_hsa_circ_116351,RMVar_hsa_circ_145629,RMVar_hsa_circ_145630 23281 RMVar_ID_23281 Human_SNP_ID_444266672 A-to-I Human chr10 - 100363625 100363625 100363625 TAGGGTCATGGTACAGATCAGATCCATGGCACACGATTACAATAGGAAGAAGTGAAAGTTGTTTT TAGGGTCATGGTACAGATCAGATCCATGGCACGCGATTACAATAGGAAGAAGTGAAAGTTGTTTT T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1448252083 Functional Loss SNV dbSNP153 33..33 33 - - - 23282 RMVar_ID_23282 Human_SNP_ID_444269409 A-to-I Human chr10 + 100375170 100375170 100375170 ATCATCTGAGGTCAGGAGTTCAAGACCAGCCTAGCCAACATGGTGAAACCCTGTTTCTATTAAAA ATCATCTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCCTGTTTCTATTAAAA A G OLMALINC Ensembl:ENSG00000235823 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1398075436 Functional Loss SNV dbSNP153 33..33 33 - - - 23283 RMVar_ID_23283 Human_SNP_ID_444270346 A-to-I Human chr10 + 100377887 100377887 100377887 AACATAGGAGAATTGCTTGAGCCCAGGAGTTCAAGACCAGCCTGGACAACATACGGAGACCCTGT AACATAGGAGAATTGCTTGAGCCCAGGAGTTCGAGACCAGCCTGGACAACATACGGAGACCCTGT A G OLMALINC Ensembl:ENSG00000235823 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs915957707 Functional Loss SNV dbSNP153 33..33 33 - - - 23284 RMVar_ID_23284 Human_SNP_ID_444270565 A-to-I Human chr10 + 100378786 100378786 100378786 CTAACTGCAACCTCCGCCTCCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTTCCGAGTAGCTGGG CTAACTGCAACCTCCGCCTCCCGGGTTCAAGCCATTCTCCTGCCTCAGCCTTCCGAGTAGCTGGG A C OLMALINC Ensembl:ENSG00000235823 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs893303084 Functional Loss SNV dbSNP153 33..33 33 - - - 23285 RMVar_ID_23285 Human_SNP_ID_444270592 A-to-I Human chr10 + 100378883 100378883 100378883 TTTTATTTTTAGTAGAGATAGGGTTTCACCATATTGGCCAGGATGGTCTTGATCTCCTGACCTCG TTTTATTTTTAGTAGAGATAGGGTTTCACCATGTTGGCCAGGATGGTCTTGATCTCCTGACCTCG A G OLMALINC Ensembl:ENSG00000235823 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs375593940 Functional Loss SNV dbSNP153 33..33 33 - - - 23286 RMVar_ID_23286 Human_SNP_ID_444270979 A-to-I Human chr10 + 100380738 100380738 100380738 GGAGGATGGCTTGAGCTTAGGAGTTTGAGGTTACAGGAAGCTATGATTGTGCCACTGCCCTCCAG GGAGGATGGCTTGAGCTTAGGAGTTTGAGGTTCCAGGAAGCTATGATTGTGCCACTGCCCTCCAG A C OLMALINC Ensembl:ENSG00000235823 lincRNA intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1009871347 Functional Loss SNV dbSNP153 33..33 33 - - - 23287 RMVar_ID_23287 Human_SNP_ID_444297637 A-to-I Human chr10 - 100493129 100493129 100493129 GACCTCGTGATCCGCCCGCCTCGGCCTCCCAAAGCGCTGGGATTATAGGCATGAGCCACCGCGCC GACCTCGTGATCCGCCCGCCTCGGCCTCCCAACGCGCTGGGATTATAGGCATGAGCCACCGCGCC T G SEC31B Ensembl:ENSG00000075826 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs974716286 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_68928 23288 RMVar_ID_23288 Human_SNP_ID_444298097 A-to-I Human chr10 - 100494888 100494888 100494888 CTGGGAGGTGGAGGTTGAAGTGAGCCCAGATCATACCACTGCACTCCAGCCTGGCAACGGAGCGA CTGGGAGGTGGAGGTTGAAGTGAGCCCAGATCGTACCACTGCACTCCAGCCTGGCAACGGAGCGA T C SEC31B Ensembl:ENSG00000075826 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1456219842 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_68928 23289 RMVar_ID_23289 Human_SNP_ID_444306133 A-to-I Human chr10 - 100527491 100527491 100527491 TCAAGTGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGATATTACAGGCACCTGCCACCACACCCA TCAAGTGATTCTCCTGCCTCAGCCTCCTGAGTCGCTGATATTACAGGCACCTGCCACCACACCCA T G NDUFB8,AL133352.1 Ensembl:ENSG00000166136,Ensembl:ENSG00000255339 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1405785547 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88793,RMVar_hsa_circ_124700,RMVar_hsa_circ_145639,RMVar_hsa_circ_145638 23290 RMVar_ID_23290 Human_SNP_ID_444309568 A-to-I Human chr10 + 100541532 100541532 100541532 GTTGTTGTTTTGTTTTTTTGAGACAGAGTCTCACTCTGTTGCCTAGGCTGGAGTGCAGTTGTGTG GTTGTTGTTTTGTTTTTTTGAGACAGAGTCTCTCTCTGTTGCCTAGGCTGGAGTGCAGTTGTGTG A T HIF1AN Ensembl:ENSG00000166135 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251390498 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122609,RMVar_hsa_circ_345636,RMVar_hsa_circ_377942,RMVar_hsa_circ_66107,RMVar_hsa_circ_145645,RMVar_hsa_circ_335334,RMVar_hsa_circ_342301 23291 RMVar_ID_23291 Human_SNP_ID_444404781 A-to-I Human chr10 + 100924268 100924268 100924268 CTGGCAATTCTGGCCACCATTCTACCAGGAATAGTGACCAAATCCAAGTGGCAGGTACCAAGGAG CTGGCAATTCTGGCCACCATTCTACCAGGAATGGTGACCAAATCCAAGTGGCAGGTACCAAGGAG A G SLF2 Ensembl:ENSG00000119906 Protein coding CDS GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1446357681 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2479035 RMVar_hsa_circ_1160,RMVar_hsa_circ_274908,RMVar_hsa_circ_112823,RMVar_hsa_circ_375468,RMVar_hsa_circ_145648,RMVar_hsa_circ_371270,RMVar_hsa_circ_356943,RMVar_hsa_circ_364715,RMVar_hsa_circ_295144,RMVar_hsa_circ_70002,RMVar_hsa_circ_60626,RMVar_hsa_circ_145653,RMVar_hsa_circ_76070,RMVar_hsa_circ_96728,RMVar_hsa_circ_145649,RMVar_hsa_circ_145651,RMVar_hsa_circ_145652,RMVar_hsa_circ_145650,RMVar_hsa_circ_282904,RMVar_hsa_circ_271342,RMVar_hsa_circ_92229,RMVar_hsa_circ_25204,RMVar_hsa_circ_62926,RMVar_hsa_circ_145655,RMVar_hsa_circ_145656,RMVar_hsa_circ_145657,RMVar_hsa_circ_145654,RMVar_hsa_circ_145661,RMVar_hsa_circ_145660,RMVar_hsa_circ_274335,RMVar_hsa_circ_350260,RMVar_hsa_circ_351020,RMVar_hsa_circ_289460,RMVar_hsa_circ_273628,RMVar_hsa_circ_145658,RMVar_hsa_circ_145659,RMVar_hsa_circ_145662 23292 RMVar_ID_23292 Human_SNP_ID_444411687 A-to-I Human chr10 + 100952042 100952042 100952042 GCGGTGGGTGGATCACTTGAGGTCAGAAGTTCAAGACCAGCCTGGCCAGCATGGTGAAACCCCGT GCGGTGGGTGGATCACTTGAGGTCAGAAGTTCGAGACCAGCCTGGCCAGCATGGTGAAACCCCGT A G SLF2 Ensembl:ENSG00000119906 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1468246317 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1160,RMVar_hsa_circ_60626,RMVar_hsa_circ_92229,RMVar_hsa_circ_145657,RMVar_hsa_circ_44341,RMVar_hsa_circ_339363,RMVar_hsa_circ_334836,RMVar_hsa_circ_341139,RMVar_hsa_circ_145672,RMVar_hsa_circ_361425,RMVar_hsa_circ_106979,RMVar_hsa_circ_145674 23293 RMVar_ID_23293 Human_SNP_ID_444411699 A-to-I Human chr10 + 100952079 100952079 100952079 CAGCCTGGCCAGCATGGTGAAACCCCGTCTCTACAGAAATACAAAAAGTTAGCCGGGCGTGTTGG CAGCCTGGCCAGCATGGTGAAACCCCGTCTCTGCAGAAATACAAAAAGTTAGCCGGGCGTGTTGG A G SLF2 Ensembl:ENSG00000119906 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs947397896 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1160,RMVar_hsa_circ_60626,RMVar_hsa_circ_92229,RMVar_hsa_circ_145657,RMVar_hsa_circ_44341,RMVar_hsa_circ_339363,RMVar_hsa_circ_334836,RMVar_hsa_circ_341139,RMVar_hsa_circ_145672,RMVar_hsa_circ_361425,RMVar_hsa_circ_106979,RMVar_hsa_circ_145674 23294 RMVar_ID_23294 Human_SNP_ID_444411701 A-to-I Human chr10 + 100952081 100952081 100952081 GCCTGGCCAGCATGGTGAAACCCCGTCTCTACAGAAATACAAAAAGTTAGCCGGGCGTGTTGGTG GCCTGGCCAGCATGGTGAAACCCCGTCTCTACTGAAATACAAAAAGTTAGCCGGGCGTGTTGGTG A T SLF2 Ensembl:ENSG00000119906 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1393237337 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1160,RMVar_hsa_circ_60626,RMVar_hsa_circ_92229,RMVar_hsa_circ_145657,RMVar_hsa_circ_44341,RMVar_hsa_circ_339363,RMVar_hsa_circ_334836,RMVar_hsa_circ_341139,RMVar_hsa_circ_145672,RMVar_hsa_circ_361425,RMVar_hsa_circ_106979,RMVar_hsa_circ_145674 23295 RMVar_ID_23295 Human_SNP_ID_444411706 A-to-I Human chr10 + 100952097 100952097 100952097 GAAACCCCGTCTCTACAGAAATACAAAAAGTTAGCCGGGCGTGTTGGTGCGTGCATGTAATCCCA GAAACCCCGTCTCTACAGAAATACAAAAAGTTTGCCGGGCGTGTTGGTGCGTGCATGTAATCCCA A T SLF2 Ensembl:ENSG00000119906 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs969400142 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1160,RMVar_hsa_circ_60626,RMVar_hsa_circ_92229,RMVar_hsa_circ_145657,RMVar_hsa_circ_44341,RMVar_hsa_circ_339363,RMVar_hsa_circ_334836,RMVar_hsa_circ_341139,RMVar_hsa_circ_145672,RMVar_hsa_circ_361425,RMVar_hsa_circ_106979,RMVar_hsa_circ_145674 23296 RMVar_ID_23296 Human_SNP_ID_444411816 A-to-I Human chr10 + 100952472 100952472 100952472 TGGAGGCTGAAGCAGGAGAACTGCCTGAACCCAGGAGGTGGAGGTTGCAGTGAGCTGAGATCACA TGGAGGCTGAAGCAGGAGAACTGCCTGAACCCGGGAGGTGGAGGTTGCAGTGAGCTGAGATCACA A G SLF2 Ensembl:ENSG00000119906 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1453373401 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1160,RMVar_hsa_circ_60626,RMVar_hsa_circ_92229,RMVar_hsa_circ_145657,RMVar_hsa_circ_44341,RMVar_hsa_circ_339363,RMVar_hsa_circ_334836,RMVar_hsa_circ_341139,RMVar_hsa_circ_145672,RMVar_hsa_circ_361425,RMVar_hsa_circ_106979,RMVar_hsa_circ_145674 23297 RMVar_ID_23297 Human_SNP_ID_444411997 A-to-I Human chr10 + 100953205 100953205 100953205 ATCCACACCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGATCATGTTGC ATCCACACCCAGCTAATTTTTGTATTTTTAGTGGAGATGGGGTTTCACCATGTTGATCATGTTGC A G SLF2 Ensembl:ENSG00000119906 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs576079018 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1160,RMVar_hsa_circ_60626,RMVar_hsa_circ_92229,RMVar_hsa_circ_145657,RMVar_hsa_circ_44341,RMVar_hsa_circ_339363,RMVar_hsa_circ_334836,RMVar_hsa_circ_341139,RMVar_hsa_circ_145672,RMVar_hsa_circ_361425,RMVar_hsa_circ_106979,RMVar_hsa_circ_145674 23298 RMVar_ID_23298 Human_SNP_ID_444412335 A-to-I Human chr10 + 100954761 100954761 100954761 GCCTAGGAGTTTAAAACCAGCTTAGGCAACATAGCAAGATGCTGTCTCTACAAAAAAACAAAAAC GCCTAGGAGTTTAAAACCAGCTTAGGCAACATTGCAAGATGCTGTCTCTACAAAAAAACAAAAAC A T SLF2 Ensembl:ENSG00000119906 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1411379403 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1160,RMVar_hsa_circ_60626,RMVar_hsa_circ_92229,RMVar_hsa_circ_145657,RMVar_hsa_circ_44341,RMVar_hsa_circ_339363,RMVar_hsa_circ_334836,RMVar_hsa_circ_341139,RMVar_hsa_circ_145672,RMVar_hsa_circ_361425,RMVar_hsa_circ_106979,RMVar_hsa_circ_145674 23299 RMVar_ID_23299 Human_SNP_ID_444419339 A-to-I Human chr10 - 100982740 100982740 100982740 TCGCCTAGGCTGGAGTGCAGTGACGTGATCTCAGCTCACTGCAACCTCCACCTCCCTGGTTCACG TCGCCTAGGCTGGAGTGCAGTGACGTGATCTCTGCTCACTGCAACCTCCACCTCCCTGGTTCACG T A AL133215.1,MRPL43 Ensembl:ENSG00000236662,Ensembl:ENSG00000055950 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs533663163 Functional Loss SNV dbSNP153 33..33 33 - - - 23300 RMVar_ID_23300 Human_SNP_ID_444419340 A-to-I Human chr10 - 100982740 100982740 100982740 TCGCCTAGGCTGGAGTGCAGTGACGTGATCTCAGCTCACTGCAACCTCCACCTCCCTGGTTCACG TCGCCTAGGCTGGAGTGCAGTGACGTGATCTCGGCTCACTGCAACCTCCACCTCCCTGGTTCACG T C AL133215.1,MRPL43 Ensembl:ENSG00000236662,Ensembl:ENSG00000055950 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs533663163 Functional Loss SNV dbSNP153 33..33 33 - - - 23301 RMVar_ID_23301 Human_SNP_ID_444425777 A-to-I Human chr10 + 101004400 101004400 101004400 AGGCCGAGGTGGGCGGATTGCTTGAGCTCGGGAGTTTGAGACCAACCTGGGTAACATGGGGAAAC AGGCCGAGGTGGGCGGATTGCTTGAGCTCGGGCGTTTGAGACCAACCTGGGTAACATGGGGAAAC A C LZTS2 Ensembl:ENSG00000107816 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1379913054 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5313088,Human_RBP_ID_24773212 23302 RMVar_ID_23302 Human_SNP_ID_444425898 A-to-I Human chr10 + 101004932 101004918 101004932 GTTGGCCAAGCTGGTCGCGAACCCCTGGCCTCAAGTGATTCACCTGCCTCGGCCTCCCAAAGTGC GTTGGCCAAGCTGGTCGCG______________AGTGATTCACCTGCCTCGGCCTCCCAAAGTGC GAACCCCTGGCCTCA G LZTS2 Ensembl:ENSG00000107816 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1284117549 Functional Loss DEL dbSNP153 20..33 33 - - - 23303 RMVar_ID_23303 Human_SNP_ID_444425902 A-to-I Human chr10 + 101004932 101004932 101004932 GTTGGCCAAGCTGGTCGCGAACCCCTGGCCTCAAGTGATTCACCTGCCTCGGCCTCCCAAAGTGC GTTGGCCAAGCTGGTCGCGAACCCCTGGCCTCGAGTGATTCACCTGCCTCGGCCTCCCAAAGTGC A G LZTS2 Ensembl:ENSG00000107816 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1317186620 Functional Loss SNV dbSNP153 33..33 33 - - - 23304 RMVar_ID_23304 Human_SNP_ID_444425933 A-to-I Human chr10 + 101005107 101005107 101005107 CTCCCTGTAGCCTCAACCCCCTGGGCTCAAGCAGTCCTCTCACCCCAGCCTCCCAAGTAGCTGAG CTCCCTGTAGCCTCAACCCCCTGGGCTCAAGCCGTCCTCTCACCCCAGCCTCCCAAGTAGCTGAG A C LZTS2 Ensembl:ENSG00000107816 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs531336251 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24773220 23305 RMVar_ID_23305 Human_SNP_ID_444425938 A-to-I Human chr10 + 101005143 101005143 101005143 CTCTCACCCCAGCCTCCCAAGTAGCTGAGACTACAGGCGCATGCCACCACACCAAGCTAATTTTT CTCTCACCCCAGCCTCCCAAGTAGCTGAGACTCCAGGCGCATGCCACCACACCAAGCTAATTTTT A C LZTS2 Ensembl:ENSG00000107816 Protein coding intron GSE47997;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 K562 cells&HepG2 cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 23474544,29129909,31158229 RNA-Seq:(High) rs1463965971 Functional Loss SNV dbSNP153 33..33 33 - - - 23306 RMVar_ID_23306 Human_SNP_ID_444429929 A-to-I Human chr10 - 101017578 101017578 101017578 GGGGTTTCACCCTGTTGCCCAGGCTAGTCTCAAATTCCTGGACTGAAGCTATCTACCCGCCTTAG GGGGTTTCACCCTGTTGCCCAGGCTAGTCTCAGATTCCTGGACTGAAGCTATCTACCCGCCTTAG T C PDZD7 Ensembl:ENSG00000186862 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1285240467 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1169582 23307 RMVar_ID_23307 Human_SNP_ID_444517308 A-to-I Human chr10 + 101358377 101358377 101358377 TCCTCCTGCCTTGGCCTCCCATTGTTGGGATTACAGGCGTGAGCCACCTTGCCAAGCCACGTTTA TCCTCCTGCCTTGGCCTCCCATTGTTGGGATTGCAGGCGTGAGCCACCTTGCCAAGCCACGTTTA A G BTRC Ensembl:ENSG00000166167 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978560555 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5917366 23308 RMVar_ID_23308 Human_SNP_ID_444518975 A-to-I Human chr10 + 101364958 101364958 101364958 TGCTCCAAAAATCTATTTAATATATTGTCCTCAGATAGAGGACATATCAGATACTAAACTGATGA TGCTCCAAAAATCTATTTAATATATTGTCCTCGGATAGAGGACATATCAGATACTAAACTGATGA A G BTRC Ensembl:ENSG00000166167 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs78033937 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11486300 23309 RMVar_ID_23309 Human_SNP_ID_444518982 A-to-I Human chr10 + 101364969 101364969 101364969 TCTATTTAATATATTGTCCTCAGATAGAGGACATATCAGATACTAAACTGATGAGAACAGATACT TCTATTTAATATATTGTCCTCAGATAGAGGACGTATCAGATACTAAACTGATGAGAACAGATACT A G BTRC Ensembl:ENSG00000166167 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs75718917 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11234811 23310 RMVar_ID_23310 Human_SNP_ID_444518983 A-to-I Human chr10 + 101364971 101364971 101364971 TATTTAATATATTGTCCTCAGATAGAGGACATATCAGATACTAAACTGATGAGAACAGATACTAC TATTTAATATATTGTCCTCAGATAGAGGACATGTCAGATACTAAACTGATGAGAACAGATACTAC A G BTRC Ensembl:ENSG00000166167 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1382357319 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11234811 23311 RMVar_ID_23311 Human_SNP_ID_444547951 A-to-I Human chr10 + 101482647 101482647 101482647 TTGATCTCCTGACGTCGTGATCCGCTTGCCTCAGCCTCCCAAAGCAATGGGATTACAGTCGTGAG TTGATCTCCTGACGTCGTGATCCGCTTGCCTCCGCCTCCCAAAGCAATGGGATTACAGTCGTGAG A C BTRC Ensembl:ENSG00000166167 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1437329415 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11235767 RMVar_hsa_circ_5634,RMVar_hsa_circ_96023,RMVar_hsa_circ_34975,RMVar_hsa_circ_145704,RMVar_hsa_circ_145705,RMVar_hsa_circ_344583 23312 RMVar_ID_23312 Human_SNP_ID_444551363 A-to-I Human chr10 + 101498283 101498283 101498283 TCAAGCAATTCCCCTGCCTCAGCCTCCCTAGTAGCTGGGACCACAGACATGTGCCACCACGCACA TCAAGCAATTCCCCTGCCTCAGCCTCCCTAGTGGCTGGGACCACAGACATGTGCCACCACGCACA A G BTRC Ensembl:ENSG00000166167 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005305082 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5634,RMVar_hsa_circ_96023,RMVar_hsa_circ_34975,RMVar_hsa_circ_145704,RMVar_hsa_circ_145705,RMVar_hsa_circ_344583 23313 RMVar_ID_23313 Human_SNP_ID_444555257 A-to-I Human chr10 + 101514511 101514511 101514511 AGAAAGCTCTGTCACCCAATCTAGAGTGCAGTAGCACAATCTAGGCTCACTATAACCTCCACCTC AGAAAGCTCTGTCACCCAATCTAGAGTGCAGTGGCACAATCTAGGCTCACTATAACCTCCACCTC A G BTRC Ensembl:ENSG00000166167 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1420506670 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5634,RMVar_hsa_circ_96023,RMVar_hsa_circ_34975,RMVar_hsa_circ_145704,RMVar_hsa_circ_145705,RMVar_hsa_circ_344583 23314 RMVar_ID_23314 Human_SNP_ID_444602003 A-to-I Human chr10 + 101717735 101717735 101717735 GAGCTCAAGTTCTCCTCCTGCCTTGGCCTTCCAAAGTGCTGGGATTACAGGTGTGAGCCCCCTGC GAGCTCAAGTTCTCCTCCTGCCTTGGCCTTCCGAAGTGCTGGGATTACAGGTGTGAGCCCCCTGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1046951660 Functional Loss SNV dbSNP153 33..33 33 - - - 23315 RMVar_ID_23315 Human_SNP_ID_444617655 A-to-I Human chr10 + 101781454 101781454 101781454 CTCACAGGCAGGTGGGAAGGGAGGCCCCGGGCATGGTGAAAATCAGAAAACCACGGCTGTGTGGA CTCACAGGCAGGTGGGAAGGGAGGCCCCGGGCGTGGTGAAAATCAGAAAACCACGGCTGTGTGGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs540518327 Functional Loss SNV dbSNP153 33..33 33 - - - 23316 RMVar_ID_23316 Human_SNP_ID_444618183 A-to-I Human chr10 - 101782881 101782876 101782882 TCCGGCCACACCCGCTCCTTCACCTTTAAGGTAGAGGAAGAGGATGATGCGGAGCACGTGCTGGC TCCGGCCACACCCGCTCCTTCACCTTTAAGG______AAGAGGATGATGCGGAGCACGTGCTGGC TCCTCTA T NPM3 Ensembl:ENSG00000107833 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs775354875 Functional Loss DEL dbSNP153 32..37 33 - - - Human_RBP_ID_368312,Human_RBP_ID_4102902,Human_RBP_ID_5918384,Human_RBP_ID_8981447,Human_RBP_ID_17679282 Human_Splice_Rec_1170256,Human_Splice_Rec_1170257,Human_Splice_Rec_1170274,Human_Splice_Rec_1170275 RMVar_hsa_circ_115577,RMVar_hsa_circ_145750 23317 RMVar_ID_23317 Human_SNP_ID_444618184 A-to-I Human chr10 - 101782881 101782881 101782881 TCCGGCCACACCCGCTCCTTCACCTTTAAGGTAGAGGAAGAGGATGATGCGGAGCACGTGCTGGC TCCGGCCACACCCGCTCCTTCACCTTTAAGGTGGAGGAAGAGGATGATGCGGAGCACGTGCTGGC T C NPM3 Ensembl:ENSG00000107833 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs960349025 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_368312,Human_RBP_ID_4102902,Human_RBP_ID_5918384,Human_RBP_ID_8981447,Human_RBP_ID_17679282 Human_Splice_Rec_1170256,Human_Splice_Rec_1170257,Human_Splice_Rec_1170274,Human_Splice_Rec_1170275 RMVar_hsa_circ_115577,RMVar_hsa_circ_145750 23318 RMVar_ID_23318 Human_SNP_ID_444619066 A-to-I Human chr10 - 101785892 101785892 101785892 CAGTTATTCTGCTTTTTGTAAAGCCGTGGCCAATTGTCTCCTGTAATGACTGTTGGTTCAGGCAT CAGTTATTCTGCTTTTTGTAAAGCCGTGGCCAGTTGTCTCCTGTAATGACTGTTGGTTCAGGCAT T C OGA Ensembl:ENSG00000198408 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs530554255 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_368368,Human_RBP_ID_1440336,Human_RBP_ID_1758773,Human_RBP_ID_2186125,Human_RBP_ID_3336625,Human_RBP_ID_4102958,Human_RBP_ID_5138372,Human_RBP_ID_5918454,Human_RBP_ID_8324177,Human_RBP_ID_8756889,Human_RBP_ID_11237450,Human_RBP_ID_19459045,Human_RBP_ID_21882400,Human_RBP_ID_22787234,Human_RBP_ID_23429629,Human_RBP_ID_27602013 Human_miRNA_ID_2026268,Human_miRNA_ID_2215911,Human_miRNA_ID_2675082,Human_miRNA_ID_2925833 RMVar_hsa_circ_145752,RMVar_hsa_circ_91447,RMVar_hsa_circ_95524,RMVar_hsa_circ_145753 23319 RMVar_ID_23319 Human_SNP_ID_444619614 A-to-I Human chr10 - 101787851 101787851 101787851 ACGGCAGCACACACTTGTAATTCTAGCACTTCAGGAGGCCGAGATAGAAGGATCACTCGAGCCCA ACGGCAGCACACACTTGTAATTCTAGCACTTCGGGAGGCCGAGATAGAAGGATCACTCGAGCCCA T C OGA Ensembl:ENSG00000198408 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1453220425 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11237508,Human_RBP_ID_24774237 RMVar_hsa_circ_145752,RMVar_hsa_circ_91447,RMVar_hsa_circ_95524,RMVar_hsa_circ_145753,RMVar_hsa_circ_145754,RMVar_hsa_circ_267163,RMVar_hsa_circ_354533,RMVar_hsa_circ_377677,RMVar_hsa_circ_300923,RMVar_hsa_circ_145755 23320 RMVar_ID_23320 Human_SNP_ID_444619619 A-to-I Human chr10 - 101787871 101787871 101787871 AGTGAAAACGGTGGCCAGGCACGGCAGCACACACTTGTAATTCTAGCACTTCAGGAGGCCGAGAT AGTGAAAACGGTGGCCAGGCACGGCAGCACACCCTTGTAATTCTAGCACTTCAGGAGGCCGAGAT T G OGA Ensembl:ENSG00000198408 Protein coding intron GSE47997;GSE38233;GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 K562 cells&HepG2 cells;cultured B-cells;cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 23474544,24183664,24183664,29129909,31158229 RNA-Seq:(High) rs1279705149 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11237508 RMVar_hsa_circ_145752,RMVar_hsa_circ_91447,RMVar_hsa_circ_95524,RMVar_hsa_circ_145753,RMVar_hsa_circ_145754,RMVar_hsa_circ_267163,RMVar_hsa_circ_354533,RMVar_hsa_circ_377677,RMVar_hsa_circ_300923,RMVar_hsa_circ_145755 23321 RMVar_ID_23321 Human_SNP_ID_444619719 A-to-I Human chr10 - 101788203 101788203 101788203 AAACTCCTGAGCTCAGGCAGTCTGCCTGCCTCAGCCTCCTAAAGTGCTAGGATTACAGGCGTGAG AAACTCCTGAGCTCAGGCAGTCTGCCTGCCTCTGCCTCCTAAAGTGCTAGGATTACAGGCGTGAG T A OGA Ensembl:ENSG00000198408 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs572764034 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11237529 RMVar_hsa_circ_145752,RMVar_hsa_circ_91447,RMVar_hsa_circ_95524,RMVar_hsa_circ_145753,RMVar_hsa_circ_145754,RMVar_hsa_circ_267163,RMVar_hsa_circ_354533,RMVar_hsa_circ_377677,RMVar_hsa_circ_300923,RMVar_hsa_circ_145755 23322 RMVar_ID_23322 Human_SNP_ID_444619883 A-to-I Human chr10 - 101788696 101788696 101788696 GAGTTTCCCTCTGTCGCCTGGGGTGGAGTGCAATGGTGCGATCTCGGCTCACTGCAACCTCCGCC GAGTTTCCCTCTGTCGCCTGGGGTGGAGTGCAGTGGTGCGATCTCGGCTCACTGCAACCTCCGCC T C OGA Ensembl:ENSG00000198408 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910323574 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11486501 RMVar_hsa_circ_145752,RMVar_hsa_circ_91447,RMVar_hsa_circ_95524,RMVar_hsa_circ_145753,RMVar_hsa_circ_145754,RMVar_hsa_circ_267163,RMVar_hsa_circ_354533,RMVar_hsa_circ_377677,RMVar_hsa_circ_300923,RMVar_hsa_circ_145755 23323 RMVar_ID_23323 Human_SNP_ID_444620084 A-to-I Human chr10 - 101789451 101789451 101789451 TCTTGTTGCCCAGGCTGGAGTGCAGTGACGCAATCTTGGCTCACCGCAACCTCCACCTCTCAGGC TCTTGTTGCCCAGGCTGGAGTGCAGTGACGCAGTCTTGGCTCACCGCAACCTCCACCTCTCAGGC T C OGA Ensembl:ENSG00000198408 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs891757920 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_145752,RMVar_hsa_circ_91447,RMVar_hsa_circ_95524,RMVar_hsa_circ_145753,RMVar_hsa_circ_145754,RMVar_hsa_circ_267163,RMVar_hsa_circ_354533,RMVar_hsa_circ_377677,RMVar_hsa_circ_300923,RMVar_hsa_circ_145755 23324 RMVar_ID_23324 Human_SNP_ID_444620150 A-to-I Human chr10 - 101789723 101789723 101789723 GCAGTCCGCCTGCCTCGGCCTCCCATACTGCTAGGATTACAAGCACGAGCCACTGTGCCTGGCCA GCAGTCCGCCTGCCTCGGCCTCCCATACTGCTGGGATTACAAGCACGAGCCACTGTGCCTGGCCA T C OGA Ensembl:ENSG00000198408 Protein coding intron GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,30559470,31158229,31158229 RNA-Seq:(High) rs1344606179 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11237591 RMVar_hsa_circ_145752,RMVar_hsa_circ_91447,RMVar_hsa_circ_95524,RMVar_hsa_circ_145753,RMVar_hsa_circ_145754,RMVar_hsa_circ_267163,RMVar_hsa_circ_354533,RMVar_hsa_circ_377677,RMVar_hsa_circ_300923,RMVar_hsa_circ_145755 23325 RMVar_ID_23325 Human_SNP_ID_444620166 A-to-I Human chr10 - 101789782 101789782 101789782 TTTTGTAGAGATGGGGTTTCGCCGTGTTGCCCAGGCTGGTCTCAAAGTCCTGAGCTCAAGCAGTC TTTTGTAGAGATGGGGTTTCGCCGTGTTGCCCGGGCTGGTCTCAAAGTCCTGAGCTCAAGCAGTC T C OGA Ensembl:ENSG00000198408 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1409722753 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_145752,RMVar_hsa_circ_91447,RMVar_hsa_circ_95524,RMVar_hsa_circ_145753,RMVar_hsa_circ_145754,RMVar_hsa_circ_267163,RMVar_hsa_circ_354533,RMVar_hsa_circ_377677,RMVar_hsa_circ_300923,RMVar_hsa_circ_145755 23326 RMVar_ID_23326 Human_SNP_ID_444620193 A-to-I Human chr10 - 101789903 101789903 101789903 ACAAACATGGCTCACTGCAGCCTTGACCTCCCAGGCTCAAGTTATCCTCTTGCATCAGCCCTGCA ACAAACATGGCTCACTGCAGCCTTGACCTCCCGGGCTCAAGTTATCCTCTTGCATCAGCCCTGCA T C OGA Ensembl:ENSG00000198408 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1489900999 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_145752,RMVar_hsa_circ_91447,RMVar_hsa_circ_95524,RMVar_hsa_circ_145753,RMVar_hsa_circ_145754,RMVar_hsa_circ_267163,RMVar_hsa_circ_354533,RMVar_hsa_circ_377677,RMVar_hsa_circ_300923,RMVar_hsa_circ_145755 23327 RMVar_ID_23327 Human_SNP_ID_444620205 A-to-I Human chr10 - 101789940 101789940 101789940 GACAGTGTCTCACCTTGTCACCCAGGAATGCAATAGCACAAACATGGCTCACTGCAGCCTTGACC GACAGTGTCTCACCTTGTCACCCAGGAATGCAGTAGCACAAACATGGCTCACTGCAGCCTTGACC T C OGA Ensembl:ENSG00000198408 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs1010350349 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_145752,RMVar_hsa_circ_91447,RMVar_hsa_circ_95524,RMVar_hsa_circ_145753,RMVar_hsa_circ_145754,RMVar_hsa_circ_267163,RMVar_hsa_circ_354533,RMVar_hsa_circ_377677,RMVar_hsa_circ_300923,RMVar_hsa_circ_145755 23328 RMVar_ID_23328 Human_SNP_ID_444620206 A-to-I Human chr10 - 101789945 101789945 101789945 TTTGAGACAGTGTCTCACCTTGTCACCCAGGAATGCAATAGCACAAACATGGCTCACTGCAGCCT TTTGAGACAGTGTCTCACCTTGTCACCCAGGAGTGCAATAGCACAAACATGGCTCACTGCAGCCT T C OGA Ensembl:ENSG00000198408 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1233987034 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_145752,RMVar_hsa_circ_91447,RMVar_hsa_circ_95524,RMVar_hsa_circ_145753,RMVar_hsa_circ_145754,RMVar_hsa_circ_267163,RMVar_hsa_circ_354533,RMVar_hsa_circ_377677,RMVar_hsa_circ_300923,RMVar_hsa_circ_145755 23329 RMVar_ID_23329 Human_SNP_ID_444620389 A-to-I Human chr10 - 101790437 101790437 101790437 CTCCATCTCTACTAAAAATACAAAAAAAAATTAGCTGGGTGTGGTGGCGGGTGCCTGTAATGCCA CTCCATCTCTACTAAAAATACAAAAAAAAATTGGCTGGGTGTGGTGGCGGGTGCCTGTAATGCCA T C OGA Ensembl:ENSG00000198408 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1310934743 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24774287 RMVar_hsa_circ_145752,RMVar_hsa_circ_91447,RMVar_hsa_circ_95524,RMVar_hsa_circ_145753,RMVar_hsa_circ_145754,RMVar_hsa_circ_267163,RMVar_hsa_circ_354533,RMVar_hsa_circ_377677,RMVar_hsa_circ_300923,RMVar_hsa_circ_145755 23330 RMVar_ID_23330 Human_SNP_ID_444622518 A-to-I Human chr10 - 101799067 101799067 101799067 GAAGATTGTATTAGTGACATTGCCCCCATGCAAACTGATGAACAGACAAACAAGGAGCAGTTTGT GAAGATTGTATTAGTGACATTGCCCCCATGCAGACTGATGAACAGACAAACAAGGAGCAGTTTGT T C OGA Ensembl:ENSG00000198408 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1190354468 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_864587,Human_RBP_ID_1758844,Human_RBP_ID_5459713,Human_RBP_ID_5520252,Human_RBP_ID_8756926,Human_RBP_ID_9360686,Human_RBP_ID_11238006,Human_RBP_ID_18237025,Human_RBP_ID_18585354,Human_RBP_ID_22029497,Human_RBP_ID_26315972,Human_RBP_ID_27802282 RMVar_hsa_circ_145772,RMVar_hsa_circ_91447,RMVar_hsa_circ_145753,RMVar_hsa_circ_145754,RMVar_hsa_circ_267163,RMVar_hsa_circ_354533,RMVar_hsa_circ_377677,RMVar_hsa_circ_300923,RMVar_hsa_circ_145755,RMVar_hsa_circ_361296,RMVar_hsa_circ_333172,RMVar_hsa_circ_310092,RMVar_hsa_circ_67795,RMVar_hsa_circ_68548,RMVar_hsa_circ_315307,RMVar_hsa_circ_377761,RMVar_hsa_circ_145756,RMVar_hsa_circ_354515,RMVar_hsa_circ_332190,RMVar_hsa_circ_279073,RMVar_hsa_circ_280263,RMVar_hsa_circ_271818,RMVar_hsa_circ_145765,RMVar_hsa_circ_145767,RMVar_hsa_circ_37372,RMVar_hsa_circ_145768,RMVar_hsa_circ_145766,RMVar_hsa_circ_145763,RMVar_hsa_circ_145764,RMVar_hsa_circ_145762,RMVar_hsa_circ_145776,RMVar_hsa_circ_273642,RMVar_hsa_circ_318924,RMVar_hsa_circ_274793,RMVar_hsa_circ_270854,RMVar_hsa_circ_272240,RMVar_hsa_circ_268003,RMVar_hsa_circ_145774,RMVar_hsa_circ_145775,RMVar_hsa_circ_145773,RMVar_hsa_circ_145781,RMVar_hsa_circ_285699,RMVar_hsa_circ_295545,RMVar_hsa_circ_327448,RMVar_hsa_circ_145771,RMVar_hsa_circ_357592,RMVar_hsa_circ_320995,RMVar_hsa_circ_290033,RMVar_hsa_circ_69248,RMVar_hsa_circ_280221,RMVar_hsa_circ_145782,RMVar_hsa_circ_145783,RMVar_hsa_circ_145777,RMVar_hsa_circ_145779,RMVar_hsa_circ_145780,RMVar_hsa_circ_145778 23331 RMVar_ID_23331 Human_SNP_ID_444623045 A-to-I Human chr10 - 101800843 101800843 101800843 TTGAACCTGTGAGGCGGAGGTTGTAGTGAGCCAAGATCCTGCCACTGCACTCCAGCCTGGGTGAT TTGAACCTGTGAGGCGGAGGTTGTAGTGAGCCGAGATCCTGCCACTGCACTCCAGCCTGGGTGAT T C OGA Ensembl:ENSG00000198408 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs906418002 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24854671 RMVar_hsa_circ_145772,RMVar_hsa_circ_91447,RMVar_hsa_circ_145753,RMVar_hsa_circ_145754,RMVar_hsa_circ_354533,RMVar_hsa_circ_377677,RMVar_hsa_circ_300923,RMVar_hsa_circ_145755,RMVar_hsa_circ_333172,RMVar_hsa_circ_310092,RMVar_hsa_circ_67795,RMVar_hsa_circ_68548,RMVar_hsa_circ_377761,RMVar_hsa_circ_145756,RMVar_hsa_circ_354515,RMVar_hsa_circ_332190,RMVar_hsa_circ_279073,RMVar_hsa_circ_280263,RMVar_hsa_circ_271818,RMVar_hsa_circ_145765,RMVar_hsa_circ_145767,RMVar_hsa_circ_37372,RMVar_hsa_circ_145768,RMVar_hsa_circ_145766,RMVar_hsa_circ_145763,RMVar_hsa_circ_145764,RMVar_hsa_circ_145776,RMVar_hsa_circ_273642,RMVar_hsa_circ_318924,RMVar_hsa_circ_270854,RMVar_hsa_circ_272240,RMVar_hsa_circ_145774,RMVar_hsa_circ_145775,RMVar_hsa_circ_145773,RMVar_hsa_circ_145786,RMVar_hsa_circ_145781,RMVar_hsa_circ_295545,RMVar_hsa_circ_327448,RMVar_hsa_circ_357592,RMVar_hsa_circ_320995,RMVar_hsa_circ_290033,RMVar_hsa_circ_280221,RMVar_hsa_circ_145782,RMVar_hsa_circ_145777,RMVar_hsa_circ_145779,RMVar_hsa_circ_145780,RMVar_hsa_circ_145778,RMVar_hsa_circ_284942,RMVar_hsa_circ_313074,RMVar_hsa_circ_348591,RMVar_hsa_circ_297606,RMVar_hsa_circ_102464,RMVar_hsa_circ_145787,RMVar_hsa_circ_145788,RMVar_hsa_circ_145785 23332 RMVar_ID_23332 Human_SNP_ID_444623055 A-to-I Human chr10 - 101800903 101800903 101800903 GGGCATGGTGGCATGCGCCTGTAGTCCCAGCTACTGGGGAGGCTCAGGTGGGAGAATTGCTTGAA GGGCATGGTGGCATGCGCCTGTAGTCCCAGCTGCTGGGGAGGCTCAGGTGGGAGAATTGCTTGAA T C OGA Ensembl:ENSG00000198408 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1348670393 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_145772,RMVar_hsa_circ_91447,RMVar_hsa_circ_145753,RMVar_hsa_circ_145754,RMVar_hsa_circ_354533,RMVar_hsa_circ_377677,RMVar_hsa_circ_300923,RMVar_hsa_circ_145755,RMVar_hsa_circ_333172,RMVar_hsa_circ_310092,RMVar_hsa_circ_67795,RMVar_hsa_circ_68548,RMVar_hsa_circ_377761,RMVar_hsa_circ_145756,RMVar_hsa_circ_354515,RMVar_hsa_circ_332190,RMVar_hsa_circ_279073,RMVar_hsa_circ_280263,RMVar_hsa_circ_271818,RMVar_hsa_circ_145765,RMVar_hsa_circ_145767,RMVar_hsa_circ_37372,RMVar_hsa_circ_145768,RMVar_hsa_circ_145766,RMVar_hsa_circ_145763,RMVar_hsa_circ_145764,RMVar_hsa_circ_145776,RMVar_hsa_circ_273642,RMVar_hsa_circ_318924,RMVar_hsa_circ_270854,RMVar_hsa_circ_272240,RMVar_hsa_circ_145774,RMVar_hsa_circ_145775,RMVar_hsa_circ_145773,RMVar_hsa_circ_145786,RMVar_hsa_circ_145781,RMVar_hsa_circ_295545,RMVar_hsa_circ_327448,RMVar_hsa_circ_357592,RMVar_hsa_circ_320995,RMVar_hsa_circ_290033,RMVar_hsa_circ_280221,RMVar_hsa_circ_145782,RMVar_hsa_circ_145777,RMVar_hsa_circ_145779,RMVar_hsa_circ_145780,RMVar_hsa_circ_145778,RMVar_hsa_circ_284942,RMVar_hsa_circ_313074,RMVar_hsa_circ_348591,RMVar_hsa_circ_297606,RMVar_hsa_circ_102464,RMVar_hsa_circ_145787,RMVar_hsa_circ_145788,RMVar_hsa_circ_145785 23333 RMVar_ID_23333 Human_SNP_ID_444623103 A-to-I Human chr10 - 101801147 101801147 101801147 ACCTCAGGTGATTTGCCCGCCTCAGCCTCCCAAAGTGCTGAGATTACAGGCATGAGCCACCATGC ACCTCAGGTGATTTGCCCGCCTCAGCCTCCCAGAGTGCTGAGATTACAGGCATGAGCCACCATGC T C OGA Ensembl:ENSG00000198408 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs993995430 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_145772,RMVar_hsa_circ_91447,RMVar_hsa_circ_145753,RMVar_hsa_circ_145754,RMVar_hsa_circ_354533,RMVar_hsa_circ_377677,RMVar_hsa_circ_300923,RMVar_hsa_circ_145755,RMVar_hsa_circ_333172,RMVar_hsa_circ_310092,RMVar_hsa_circ_67795,RMVar_hsa_circ_68548,RMVar_hsa_circ_377761,RMVar_hsa_circ_145756,RMVar_hsa_circ_354515,RMVar_hsa_circ_332190,RMVar_hsa_circ_279073,RMVar_hsa_circ_280263,RMVar_hsa_circ_271818,RMVar_hsa_circ_145765,RMVar_hsa_circ_145767,RMVar_hsa_circ_37372,RMVar_hsa_circ_145768,RMVar_hsa_circ_145766,RMVar_hsa_circ_145763,RMVar_hsa_circ_145764,RMVar_hsa_circ_145776,RMVar_hsa_circ_273642,RMVar_hsa_circ_318924,RMVar_hsa_circ_270854,RMVar_hsa_circ_272240,RMVar_hsa_circ_145774,RMVar_hsa_circ_145775,RMVar_hsa_circ_145773,RMVar_hsa_circ_145786,RMVar_hsa_circ_145781,RMVar_hsa_circ_295545,RMVar_hsa_circ_327448,RMVar_hsa_circ_357592,RMVar_hsa_circ_320995,RMVar_hsa_circ_290033,RMVar_hsa_circ_280221,RMVar_hsa_circ_145782,RMVar_hsa_circ_145777,RMVar_hsa_circ_145779,RMVar_hsa_circ_145780,RMVar_hsa_circ_145778,RMVar_hsa_circ_284942,RMVar_hsa_circ_313074,RMVar_hsa_circ_348591,RMVar_hsa_circ_297606,RMVar_hsa_circ_102464,RMVar_hsa_circ_145787,RMVar_hsa_circ_145788,RMVar_hsa_circ_145785 23334 RMVar_ID_23334 Human_SNP_ID_444623112 A-to-I Human chr10 - 101801194 101801194 101801194 TAGAGATGGGGTTTTACCATGTTGGCCAGGCTAGTCTCAAACTGCAGACCTCAGGTGATTTGCCC TAGAGATGGGGTTTTACCATGTTGGCCAGGCTCGTCTCAAACTGCAGACCTCAGGTGATTTGCCC T G OGA Ensembl:ENSG00000198408 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1355673650 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_145772,RMVar_hsa_circ_91447,RMVar_hsa_circ_145753,RMVar_hsa_circ_145754,RMVar_hsa_circ_354533,RMVar_hsa_circ_377677,RMVar_hsa_circ_300923,RMVar_hsa_circ_145755,RMVar_hsa_circ_333172,RMVar_hsa_circ_310092,RMVar_hsa_circ_67795,RMVar_hsa_circ_68548,RMVar_hsa_circ_377761,RMVar_hsa_circ_145756,RMVar_hsa_circ_354515,RMVar_hsa_circ_332190,RMVar_hsa_circ_279073,RMVar_hsa_circ_280263,RMVar_hsa_circ_271818,RMVar_hsa_circ_145765,RMVar_hsa_circ_145767,RMVar_hsa_circ_37372,RMVar_hsa_circ_145768,RMVar_hsa_circ_145766,RMVar_hsa_circ_145763,RMVar_hsa_circ_145764,RMVar_hsa_circ_145776,RMVar_hsa_circ_273642,RMVar_hsa_circ_318924,RMVar_hsa_circ_270854,RMVar_hsa_circ_272240,RMVar_hsa_circ_145774,RMVar_hsa_circ_145775,RMVar_hsa_circ_145773,RMVar_hsa_circ_145786,RMVar_hsa_circ_145781,RMVar_hsa_circ_295545,RMVar_hsa_circ_327448,RMVar_hsa_circ_357592,RMVar_hsa_circ_320995,RMVar_hsa_circ_290033,RMVar_hsa_circ_280221,RMVar_hsa_circ_145782,RMVar_hsa_circ_145777,RMVar_hsa_circ_145779,RMVar_hsa_circ_145780,RMVar_hsa_circ_145778,RMVar_hsa_circ_284942,RMVar_hsa_circ_313074,RMVar_hsa_circ_348591,RMVar_hsa_circ_297606,RMVar_hsa_circ_102464,RMVar_hsa_circ_145787,RMVar_hsa_circ_145788,RMVar_hsa_circ_145785 23335 RMVar_ID_23335 Human_SNP_ID_444623156 A-to-I Human chr10 - 101801353 101801353 101801353 AGTCTTGCTCTTGTTGCTCAGGCTGGAGTGCAATGGCCCGATCTCAGCTCACTGCAACCTTTGAC AGTCTTGCTCTTGTTGCTCAGGCTGGAGTGCAGTGGCCCGATCTCAGCTCACTGCAACCTTTGAC T C OGA Ensembl:ENSG00000198408 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs969422985 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_145772,RMVar_hsa_circ_91447,RMVar_hsa_circ_145753,RMVar_hsa_circ_145754,RMVar_hsa_circ_354533,RMVar_hsa_circ_377677,RMVar_hsa_circ_300923,RMVar_hsa_circ_145755,RMVar_hsa_circ_333172,RMVar_hsa_circ_310092,RMVar_hsa_circ_67795,RMVar_hsa_circ_68548,RMVar_hsa_circ_377761,RMVar_hsa_circ_145756,RMVar_hsa_circ_354515,RMVar_hsa_circ_332190,RMVar_hsa_circ_279073,RMVar_hsa_circ_280263,RMVar_hsa_circ_271818,RMVar_hsa_circ_145765,RMVar_hsa_circ_145767,RMVar_hsa_circ_37372,RMVar_hsa_circ_145768,RMVar_hsa_circ_145766,RMVar_hsa_circ_145763,RMVar_hsa_circ_145764,RMVar_hsa_circ_145776,RMVar_hsa_circ_273642,RMVar_hsa_circ_318924,RMVar_hsa_circ_270854,RMVar_hsa_circ_272240,RMVar_hsa_circ_145774,RMVar_hsa_circ_145775,RMVar_hsa_circ_145773,RMVar_hsa_circ_145786,RMVar_hsa_circ_145781,RMVar_hsa_circ_295545,RMVar_hsa_circ_327448,RMVar_hsa_circ_357592,RMVar_hsa_circ_320995,RMVar_hsa_circ_290033,RMVar_hsa_circ_280221,RMVar_hsa_circ_145782,RMVar_hsa_circ_145777,RMVar_hsa_circ_145779,RMVar_hsa_circ_145780,RMVar_hsa_circ_145778,RMVar_hsa_circ_284942,RMVar_hsa_circ_313074,RMVar_hsa_circ_348591,RMVar_hsa_circ_297606,RMVar_hsa_circ_102464,RMVar_hsa_circ_145787,RMVar_hsa_circ_145788,RMVar_hsa_circ_145785 23336 RMVar_ID_23336 Human_SNP_ID_444624276 A-to-I Human chr10 - 101805250 101805250 101805250 GGGGAGCCTGAGGTGGAAGCCCCCAGGAGTTCAAGACCAGCTTAGACAACATAGAGAGACTGTAG GGGGAGCCTGAGGTGGAAGCCCCCAGGAGTTCCAGACCAGCTTAGACAACATAGAGAGACTGTAG T G OGA Ensembl:ENSG00000198408 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs951923373 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11238135 RMVar_hsa_circ_145772,RMVar_hsa_circ_91447,RMVar_hsa_circ_145753,RMVar_hsa_circ_145754,RMVar_hsa_circ_354533,RMVar_hsa_circ_377677,RMVar_hsa_circ_300923,RMVar_hsa_circ_145755,RMVar_hsa_circ_333172,RMVar_hsa_circ_310092,RMVar_hsa_circ_67795,RMVar_hsa_circ_68548,RMVar_hsa_circ_377761,RMVar_hsa_circ_145756,RMVar_hsa_circ_354515,RMVar_hsa_circ_332190,RMVar_hsa_circ_279073,RMVar_hsa_circ_280263,RMVar_hsa_circ_271818,RMVar_hsa_circ_145765,RMVar_hsa_circ_145767,RMVar_hsa_circ_145768,RMVar_hsa_circ_145766,RMVar_hsa_circ_145764,RMVar_hsa_circ_145776,RMVar_hsa_circ_273642,RMVar_hsa_circ_318924,RMVar_hsa_circ_270854,RMVar_hsa_circ_272240,RMVar_hsa_circ_145774,RMVar_hsa_circ_145775,RMVar_hsa_circ_145773,RMVar_hsa_circ_145786,RMVar_hsa_circ_145781,RMVar_hsa_circ_295545,RMVar_hsa_circ_327448,RMVar_hsa_circ_357592,RMVar_hsa_circ_290033,RMVar_hsa_circ_280221,RMVar_hsa_circ_145777,RMVar_hsa_circ_145779,RMVar_hsa_circ_145780,RMVar_hsa_circ_145778,RMVar_hsa_circ_284942,RMVar_hsa_circ_313074,RMVar_hsa_circ_297606,RMVar_hsa_circ_102464,RMVar_hsa_circ_145787,RMVar_hsa_circ_145788,RMVar_hsa_circ_298962,RMVar_hsa_circ_352986,RMVar_hsa_circ_365432,RMVar_hsa_circ_366371,RMVar_hsa_circ_331351,RMVar_hsa_circ_145791,RMVar_hsa_circ_145790 23337 RMVar_ID_23337 Human_SNP_ID_444625806 A-to-I Human chr10 - 101810872 101810872 101810872 AGCCTGGGCAATATGGCAAAACCCTCATCTCTACTAAACAAAAATTAGCCGGGTATGCCTGTAAT AGCCTGGGCAATATGGCAAAACCCTCATCTCTGCTAAACAAAAATTAGCCGGGTATGCCTGTAAT T C OGA Ensembl:ENSG00000198408 Protein coding intron GSE47997;GSE107867 K562 cells&HepG2 cells;ASD brains,temporal_cortex - 23474544,30559470 RNA-Seq:(High) rs1237130260 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24774668 RMVar_hsa_circ_91447,RMVar_hsa_circ_145753,RMVar_hsa_circ_377677,RMVar_hsa_circ_67795,RMVar_hsa_circ_68548,RMVar_hsa_circ_332190,RMVar_hsa_circ_271818,RMVar_hsa_circ_145768,RMVar_hsa_circ_145776,RMVar_hsa_circ_273642,RMVar_hsa_circ_318924,RMVar_hsa_circ_145775,RMVar_hsa_circ_295545,RMVar_hsa_circ_327448,RMVar_hsa_circ_145777,RMVar_hsa_circ_313074,RMVar_hsa_circ_102464,RMVar_hsa_circ_145788,RMVar_hsa_circ_352986,RMVar_hsa_circ_365432,RMVar_hsa_circ_145791,RMVar_hsa_circ_11375,RMVar_hsa_circ_329858,RMVar_hsa_circ_343243,RMVar_hsa_circ_283899,RMVar_hsa_circ_95277,RMVar_hsa_circ_145795,RMVar_hsa_circ_145796 23338 RMVar_ID_23338 Human_SNP_ID_444625809 A-to-I Human chr10 - 101810886 101810886 101810886 AGGAGTTCGAGACCAGCCTGGGCAATATGGCAAAACCCTCATCTCTACTAAACAAAAATTAGCCG AGGAGTTCGAGACCAGCCTGGGCAATATGGCAGAACCCTCATCTCTACTAAACAAAAATTAGCCG T C OGA Ensembl:ENSG00000198408 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1020462883 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24854687 RMVar_hsa_circ_91447,RMVar_hsa_circ_145753,RMVar_hsa_circ_377677,RMVar_hsa_circ_67795,RMVar_hsa_circ_68548,RMVar_hsa_circ_332190,RMVar_hsa_circ_271818,RMVar_hsa_circ_145768,RMVar_hsa_circ_145776,RMVar_hsa_circ_273642,RMVar_hsa_circ_318924,RMVar_hsa_circ_145775,RMVar_hsa_circ_295545,RMVar_hsa_circ_327448,RMVar_hsa_circ_145777,RMVar_hsa_circ_313074,RMVar_hsa_circ_102464,RMVar_hsa_circ_145788,RMVar_hsa_circ_352986,RMVar_hsa_circ_365432,RMVar_hsa_circ_145791,RMVar_hsa_circ_11375,RMVar_hsa_circ_329858,RMVar_hsa_circ_343243,RMVar_hsa_circ_283899,RMVar_hsa_circ_95277,RMVar_hsa_circ_145795,RMVar_hsa_circ_145796 23339 RMVar_ID_23339 Human_SNP_ID_444625818 A-to-I Human chr10 - 101810928 101810928 101810928 CCAACACTGTAAGAGGCTAAGGCAGGCGGATCACTTGAGGCCAGGAGTTCGAGACCAGCCTGGGC CCAACACTGTAAGAGGCTAAGGCAGGCGGATCGCTTGAGGCCAGGAGTTCGAGACCAGCCTGGGC T C OGA Ensembl:ENSG00000198408 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs933957550 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9569672,Human_RBP_ID_17559180 RMVar_hsa_circ_91447,RMVar_hsa_circ_145753,RMVar_hsa_circ_377677,RMVar_hsa_circ_67795,RMVar_hsa_circ_68548,RMVar_hsa_circ_332190,RMVar_hsa_circ_271818,RMVar_hsa_circ_145768,RMVar_hsa_circ_145776,RMVar_hsa_circ_273642,RMVar_hsa_circ_318924,RMVar_hsa_circ_145775,RMVar_hsa_circ_295545,RMVar_hsa_circ_327448,RMVar_hsa_circ_145777,RMVar_hsa_circ_313074,RMVar_hsa_circ_102464,RMVar_hsa_circ_145788,RMVar_hsa_circ_352986,RMVar_hsa_circ_365432,RMVar_hsa_circ_145791,RMVar_hsa_circ_11375,RMVar_hsa_circ_329858,RMVar_hsa_circ_343243,RMVar_hsa_circ_283899,RMVar_hsa_circ_95277,RMVar_hsa_circ_145795,RMVar_hsa_circ_145796 23340 RMVar_ID_23340 Human_SNP_ID_444625824 A-to-I Human chr10 - 101810950 101810950 101810950 ACCATGGCTCATGCCTGCAATCCCAACACTGTAAGAGGCTAAGGCAGGCGGATCACTTGAGGCCA ACCATGGCTCATGCCTGCAATCCCAACACTGTTAGAGGCTAAGGCAGGCGGATCACTTGAGGCCA T A OGA Ensembl:ENSG00000198408 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs535233364 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11238361,Human_RBP_ID_17559180,Human_RBP_ID_24854688 RMVar_hsa_circ_91447,RMVar_hsa_circ_145753,RMVar_hsa_circ_377677,RMVar_hsa_circ_67795,RMVar_hsa_circ_68548,RMVar_hsa_circ_332190,RMVar_hsa_circ_271818,RMVar_hsa_circ_145768,RMVar_hsa_circ_145776,RMVar_hsa_circ_273642,RMVar_hsa_circ_318924,RMVar_hsa_circ_145775,RMVar_hsa_circ_295545,RMVar_hsa_circ_327448,RMVar_hsa_circ_145777,RMVar_hsa_circ_313074,RMVar_hsa_circ_102464,RMVar_hsa_circ_145788,RMVar_hsa_circ_352986,RMVar_hsa_circ_365432,RMVar_hsa_circ_145791,RMVar_hsa_circ_11375,RMVar_hsa_circ_329858,RMVar_hsa_circ_343243,RMVar_hsa_circ_283899,RMVar_hsa_circ_95277,RMVar_hsa_circ_145795,RMVar_hsa_circ_145796 23341 RMVar_ID_23341 Human_SNP_ID_444625829 A-to-I Human chr10 - 101810957 101810957 101810957 ATCCAGTACCATGGCTCATGCCTGCAATCCCAACACTGTAAGAGGCTAAGGCAGGCGGATCACTT ATCCAGTACCATGGCTCATGCCTGCAATCCCAGCACTGTAAGAGGCTAAGGCAGGCGGATCACTT T C OGA Ensembl:ENSG00000198408 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs894294126 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11238362,Human_RBP_ID_17559180 RMVar_hsa_circ_91447,RMVar_hsa_circ_145753,RMVar_hsa_circ_377677,RMVar_hsa_circ_67795,RMVar_hsa_circ_68548,RMVar_hsa_circ_332190,RMVar_hsa_circ_271818,RMVar_hsa_circ_145768,RMVar_hsa_circ_145776,RMVar_hsa_circ_273642,RMVar_hsa_circ_318924,RMVar_hsa_circ_145775,RMVar_hsa_circ_295545,RMVar_hsa_circ_327448,RMVar_hsa_circ_145777,RMVar_hsa_circ_313074,RMVar_hsa_circ_102464,RMVar_hsa_circ_145788,RMVar_hsa_circ_352986,RMVar_hsa_circ_365432,RMVar_hsa_circ_145791,RMVar_hsa_circ_11375,RMVar_hsa_circ_329858,RMVar_hsa_circ_343243,RMVar_hsa_circ_283899,RMVar_hsa_circ_95277,RMVar_hsa_circ_145795,RMVar_hsa_circ_145796 23342 RMVar_ID_23342 Human_SNP_ID_444625832 A-to-I Human chr10 - 101810963 101810963 101810963 AGCAAGATCCAGTACCATGGCTCATGCCTGCAATCCCAACACTGTAAGAGGCTAAGGCAGGCGGA AGCAAGATCCAGTACCATGGCTCATGCCTGCAGTCCCAACACTGTAAGAGGCTAAGGCAGGCGGA T C OGA Ensembl:ENSG00000198408 Protein coding intron GSE38233;GSE107867 cultured B-cells;ASD brains,temporal_cortex - 24183664,30559470 RNA-Seq:(High) rs952841918 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11238362,Human_RBP_ID_17559180 RMVar_hsa_circ_91447,RMVar_hsa_circ_145753,RMVar_hsa_circ_377677,RMVar_hsa_circ_67795,RMVar_hsa_circ_68548,RMVar_hsa_circ_332190,RMVar_hsa_circ_271818,RMVar_hsa_circ_145768,RMVar_hsa_circ_145776,RMVar_hsa_circ_273642,RMVar_hsa_circ_318924,RMVar_hsa_circ_145775,RMVar_hsa_circ_295545,RMVar_hsa_circ_327448,RMVar_hsa_circ_145777,RMVar_hsa_circ_313074,RMVar_hsa_circ_102464,RMVar_hsa_circ_145788,RMVar_hsa_circ_352986,RMVar_hsa_circ_365432,RMVar_hsa_circ_145791,RMVar_hsa_circ_11375,RMVar_hsa_circ_329858,RMVar_hsa_circ_343243,RMVar_hsa_circ_283899,RMVar_hsa_circ_95277,RMVar_hsa_circ_145795,RMVar_hsa_circ_145796 23343 RMVar_ID_23343 Human_SNP_ID_444626296 A-to-I Human chr10 - 101812706 101812706 101812706 AGAAGTGCTGGAGCTGGGCTAGGCCCAGGGCAAGGCAAGTGAGGCACGTACCTTGGGTGCAAATT AGAAGTGCTGGAGCTGGGCTAGGCCCAGGGCACGGCAAGTGAGGCACGTACCTTGGGTGCAAATT T G OGA Ensembl:ENSG00000198408 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1344270548 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5918796,Human_RBP_ID_11238465 RMVar_hsa_circ_91447,RMVar_hsa_circ_145753,RMVar_hsa_circ_377677,RMVar_hsa_circ_67795,RMVar_hsa_circ_68548,RMVar_hsa_circ_332190,RMVar_hsa_circ_271818,RMVar_hsa_circ_145768,RMVar_hsa_circ_145776,RMVar_hsa_circ_273642,RMVar_hsa_circ_318924,RMVar_hsa_circ_145775,RMVar_hsa_circ_295545,RMVar_hsa_circ_327448,RMVar_hsa_circ_145777,RMVar_hsa_circ_313074,RMVar_hsa_circ_102464,RMVar_hsa_circ_145788,RMVar_hsa_circ_352986,RMVar_hsa_circ_365432,RMVar_hsa_circ_145791,RMVar_hsa_circ_11375,RMVar_hsa_circ_329858,RMVar_hsa_circ_343243,RMVar_hsa_circ_283899,RMVar_hsa_circ_95277,RMVar_hsa_circ_116156,RMVar_hsa_circ_145795,RMVar_hsa_circ_145796,RMVar_hsa_circ_145798 23344 RMVar_ID_23344 Human_SNP_ID_444628346 A-to-I Human chr10 - 101819782 101819782 101819782 AAAATTAGCCGGGTGTGGTGGCGGGTGCCTGTAGTCTCAGCTACTCGAGAGGTTGAGGCAGGAGA AAAATTAGCCGGGTGTGGTGGCGGGTGCCTGTTGTCTCAGCTACTCGAGAGGTTGAGGCAGGAGA T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973807559 Functional Loss SNV dbSNP153 33..33 33 - - - 23345 RMVar_ID_23345 Human_SNP_ID_444628347 A-to-I Human chr10 - 101819782 101819782 101819782 AAAATTAGCCGGGTGTGGTGGCGGGTGCCTGTAGTCTCAGCTACTCGAGAGGTTGAGGCAGGAGA AAAATTAGCCGGGTGTGGTGGCGGGTGCCTGTGGTCTCAGCTACTCGAGAGGTTGAGGCAGGAGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973807559 Functional Loss SNV dbSNP153 33..33 33 - - - 23346 RMVar_ID_23346 Human_SNP_ID_444632512 A-to-I Human chr10 - 101836387 101836387 101836387 AAAATATAAAAATCAGCTGGGCGTGGTGGTGCACGCCTGTAATCCCAGCTATTCGGTGGCTGAGG AAAATATAAAAATCAGCTGGGCGTGGTGGTGCGCGCCTGTAATCCCAGCTATTCGGTGGCTGAGG T C KCNIP2 Ensembl:ENSG00000120049 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1232474852 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24774894 23347 RMVar_ID_23347 Human_SNP_ID_444668713 A-to-I Human chr10 - 101987997 101987997 101987997 GGGCCTCTCAAAAGGATGCTTTTTAAGGAATAAAGGTAATATGCATACTTGAGGATCACATTAAC GGGCCTCTCAAAAGGATGCTTTTTAAGGAATAGAGGTAATATGCATACTTGAGGATCACATTAAC T C ARMH3 Ensembl:ENSG00000120029 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1297577949 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3860,RMVar_hsa_circ_41123,RMVar_hsa_circ_145800,RMVar_hsa_circ_121892,RMVar_hsa_circ_331327,RMVar_hsa_circ_345206,RMVar_hsa_circ_339782,RMVar_hsa_circ_322209,RMVar_hsa_circ_283837,RMVar_hsa_circ_45304,RMVar_hsa_circ_115346,RMVar_hsa_circ_145809,RMVar_hsa_circ_104032,RMVar_hsa_circ_351688,RMVar_hsa_circ_377131,RMVar_hsa_circ_378185,RMVar_hsa_circ_331939,RMVar_hsa_circ_340819,RMVar_hsa_circ_305248,RMVar_hsa_circ_267860,RMVar_hsa_circ_122940,RMVar_hsa_circ_13497,RMVar_hsa_circ_44423,RMVar_hsa_circ_35976,RMVar_hsa_circ_145811,RMVar_hsa_circ_145812,RMVar_hsa_circ_145813,RMVar_hsa_circ_145810,RMVar_hsa_circ_292007,RMVar_hsa_circ_335824,RMVar_hsa_circ_342823,RMVar_hsa_circ_302951,RMVar_hsa_circ_285592,RMVar_hsa_circ_59556,RMVar_hsa_circ_145815,RMVar_hsa_circ_145816,RMVar_hsa_circ_145814,RMVar_hsa_circ_145825,RMVar_hsa_circ_278023,RMVar_hsa_circ_320024,RMVar_hsa_circ_145819,RMVar_hsa_circ_88302,RMVar_hsa_circ_327024,RMVar_hsa_circ_367034,RMVar_hsa_circ_145818,RMVar_hsa_circ_337469,RMVar_hsa_circ_321116,RMVar_hsa_circ_314880,RMVar_hsa_circ_316580,RMVar_hsa_circ_314477,RMVar_hsa_circ_43104,RMVar_hsa_circ_269714,RMVar_hsa_circ_145826,RMVar_hsa_circ_145827,RMVar_hsa_circ_145821,RMVar_hsa_circ_145823,RMVar_hsa_circ_145824,RMVar_hsa_circ_145822,RMVar_hsa_circ_145828,RMVar_hsa_circ_145820 23348 RMVar_ID_23348 Human_SNP_ID_444676087 A-to-I Human chr10 - 102018913 102018913 102018913 TCACTCCGTTGCCCAGGATGGAGTGCAATGGCATGATCTTGGCTCACTGCAACCTCTGTTTCCCG TCACTCCGTTGCCCAGGATGGAGTGCAATGGCTTGATCTTGGCTCACTGCAACCTCTGTTTCCCG T A ARMH3 Ensembl:ENSG00000120029 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965247776 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_145800,RMVar_hsa_circ_121892,RMVar_hsa_circ_331327,RMVar_hsa_circ_283837,RMVar_hsa_circ_351688,RMVar_hsa_circ_378185,RMVar_hsa_circ_340819,RMVar_hsa_circ_145813,RMVar_hsa_circ_335824,RMVar_hsa_circ_302951,RMVar_hsa_circ_285592,RMVar_hsa_circ_145814,RMVar_hsa_circ_320024,RMVar_hsa_circ_367034,RMVar_hsa_circ_316580,RMVar_hsa_circ_145821,RMVar_hsa_circ_145822,RMVar_hsa_circ_304509,RMVar_hsa_circ_344434,RMVar_hsa_circ_145820,RMVar_hsa_circ_328288,RMVar_hsa_circ_45627,RMVar_hsa_circ_145834,RMVar_hsa_circ_74185,RMVar_hsa_circ_31159,RMVar_hsa_circ_268282,RMVar_hsa_circ_353113,RMVar_hsa_circ_347283,RMVar_hsa_circ_329677,RMVar_hsa_circ_145845,RMVar_hsa_circ_145846,RMVar_hsa_circ_354058,RMVar_hsa_circ_295901,RMVar_hsa_circ_145850,RMVar_hsa_circ_145848,RMVar_hsa_circ_145849,RMVar_hsa_circ_332038,RMVar_hsa_circ_358882,RMVar_hsa_circ_101278,RMVar_hsa_circ_343710 23349 RMVar_ID_23349 Human_SNP_ID_444676088 A-to-I Human chr10 - 102018913 102018913 102018913 TCACTCCGTTGCCCAGGATGGAGTGCAATGGCATGATCTTGGCTCACTGCAACCTCTGTTTCCCG TCACTCCGTTGCCCAGGATGGAGTGCAATGGCCTGATCTTGGCTCACTGCAACCTCTGTTTCCCG T G ARMH3 Ensembl:ENSG00000120029 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965247776 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_145800,RMVar_hsa_circ_121892,RMVar_hsa_circ_331327,RMVar_hsa_circ_283837,RMVar_hsa_circ_351688,RMVar_hsa_circ_378185,RMVar_hsa_circ_340819,RMVar_hsa_circ_145813,RMVar_hsa_circ_335824,RMVar_hsa_circ_302951,RMVar_hsa_circ_285592,RMVar_hsa_circ_145814,RMVar_hsa_circ_320024,RMVar_hsa_circ_367034,RMVar_hsa_circ_316580,RMVar_hsa_circ_145821,RMVar_hsa_circ_145822,RMVar_hsa_circ_304509,RMVar_hsa_circ_344434,RMVar_hsa_circ_145820,RMVar_hsa_circ_328288,RMVar_hsa_circ_45627,RMVar_hsa_circ_145834,RMVar_hsa_circ_74185,RMVar_hsa_circ_31159,RMVar_hsa_circ_268282,RMVar_hsa_circ_353113,RMVar_hsa_circ_347283,RMVar_hsa_circ_329677,RMVar_hsa_circ_145845,RMVar_hsa_circ_145846,RMVar_hsa_circ_354058,RMVar_hsa_circ_295901,RMVar_hsa_circ_145850,RMVar_hsa_circ_145848,RMVar_hsa_circ_145849,RMVar_hsa_circ_332038,RMVar_hsa_circ_358882,RMVar_hsa_circ_101278,RMVar_hsa_circ_343710 23350 RMVar_ID_23350 Human_SNP_ID_444679110 A-to-I Human chr10 - 102030588 102030588 102030588 CTCCTGCCTCAGCCTGCTGAATAGCTGGGATTACAGGCATCTGCCTCCACACTTGGCTAATTTTT CTCCTGCCTCAGCCTGCTGAATAGCTGGGATTGCAGGCATCTGCCTCCACACTTGGCTAATTTTT T C ARMH3 Ensembl:ENSG00000120029 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs921126158 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_351688,RMVar_hsa_circ_335824,RMVar_hsa_circ_316580,RMVar_hsa_circ_145820,RMVar_hsa_circ_328288,RMVar_hsa_circ_45627,RMVar_hsa_circ_74185,RMVar_hsa_circ_268282,RMVar_hsa_circ_353113,RMVar_hsa_circ_347283,RMVar_hsa_circ_145846,RMVar_hsa_circ_96971,RMVar_hsa_circ_358882,RMVar_hsa_circ_303577,RMVar_hsa_circ_269909,RMVar_hsa_circ_145859,RMVar_hsa_circ_287359,RMVar_hsa_circ_145852,RMVar_hsa_circ_145853,RMVar_hsa_circ_145851,RMVar_hsa_circ_348622,RMVar_hsa_circ_304927,RMVar_hsa_circ_357494,RMVar_hsa_circ_267318,RMVar_hsa_circ_145860,RMVar_hsa_circ_145862,RMVar_hsa_circ_340044,RMVar_hsa_circ_288623,RMVar_hsa_circ_145861 23351 RMVar_ID_23351 Human_SNP_ID_444681459 A-to-I Human chr10 - 102038269 102038269 102038269 TAACATGGCGAAACCCTGTCTCTACTAAAAATACAAAAAATTAGCTGAGCATGGTGGTGGGCGCC TAACATGGCGAAACCCTGTCTCTACTAAAAATGCAAAAAATTAGCTGAGCATGGTGGTGGGCGCC T C ARMH3 Ensembl:ENSG00000120029 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1489583206 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_351688,RMVar_hsa_circ_335824,RMVar_hsa_circ_316580,RMVar_hsa_circ_145820,RMVar_hsa_circ_328288,RMVar_hsa_circ_353113,RMVar_hsa_circ_347283,RMVar_hsa_circ_145846,RMVar_hsa_circ_358882,RMVar_hsa_circ_269909,RMVar_hsa_circ_145851,RMVar_hsa_circ_304927,RMVar_hsa_circ_357494,RMVar_hsa_circ_145860,RMVar_hsa_circ_145862,RMVar_hsa_circ_288623,RMVar_hsa_circ_145863,RMVar_hsa_circ_334690 23352 RMVar_ID_23352 Human_SNP_ID_444707666 A-to-I Human chr10 + 102134759 102134759 102134759 GGCCAGAATCTCAAGGCAATGCCCAGCTCTCTATGAACCATTCATCTTCACCTCCATCAGGTGTC GGCCAGAATCTCAAGGCAATGCCCAGCTCTCTGTGAACCATTCATCTTCACCTCCATCAGGTGTC A G PPRC1 Ensembl:ENSG00000148840 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215931850 Functional Loss SNV dbSNP153 33..33 33 - - - 23353 RMVar_ID_23353 Human_SNP_ID_444708252 A-to-I Human chr10 + 102137155 102137155 102137155 GAGATTTGGAGTTTGAGACCAGCCTGGCCAATAAGGTGAAACCCTGTCTCTACTAAAAATACAAA GAGATTTGGAGTTTGAGACCAGCCTGGCCAATCAGGTGAAACCCTGTCTCTACTAAAAATACAAA A C PPRC1 Ensembl:ENSG00000148840 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1484461916 Functional Loss SNV dbSNP153 33..33 33 - - - 23354 RMVar_ID_23354 Human_SNP_ID_444738010 A-to-I Human chr10 + 102252586 102252586 102252586 GTAGGAATGATGTGGCGTGGTGGCCCACACCTATAATCCCAGCATTTTGGGAGGCCAAGGCAGGC GTAGGAATGATGTGGCGTGGTGGCCCACACCTGTAATCCCAGCATTTTGGGAGGCCAAGGCAGGC A G GBF1 Ensembl:ENSG00000107862 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs903787094 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_145902,RMVar_hsa_circ_96447,RMVar_hsa_circ_113206,RMVar_hsa_circ_145903 23355 RMVar_ID_23355 Human_SNP_ID_444742184 A-to-I Human chr10 + 102271404 102271404 102271404 CAGGATCTTGCTGTGTTTCCCAGGCTGTTCTCAAGCTCTTGGCCTCAAGCAATCCTCCCACCTTA CAGGATCTTGCTGTGTTTCCCAGGCTGTTCTCCAGCTCTTGGCCTCAAGCAATCCTCCCACCTTA A C GBF1 Ensembl:ENSG00000107862 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037070231 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3336914,Human_RBP_ID_11242202 RMVar_hsa_circ_145902,RMVar_hsa_circ_96447,RMVar_hsa_circ_113206,RMVar_hsa_circ_145903,RMVar_hsa_circ_145905,RMVar_hsa_circ_337164,RMVar_hsa_circ_24912 23356 RMVar_ID_23356 Human_SNP_ID_444744124 A-to-I Human chr10 + 102279981 102279981 102279981 CTCTACTAAATTTTTTTTTGTTTTAATTAGCCAGGCATGGTGGCACACACCAGTAGTCCCAGCTA CTCTACTAAATTTTTTTTTGTTTTAATTAGCCGGGCATGGTGGCACACACCAGTAGTCCCAGCTA A G GBF1 Ensembl:ENSG00000107862 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1267872650 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11242449,Human_RBP_ID_17559187 RMVar_hsa_circ_145902,RMVar_hsa_circ_96447,RMVar_hsa_circ_113206,RMVar_hsa_circ_145903,RMVar_hsa_circ_145905,RMVar_hsa_circ_337164,RMVar_hsa_circ_24912 23357 RMVar_ID_23357 Human_SNP_ID_444744127 A-to-I Human chr10 + 102279993 102279993 102279993 TTTTTTTGTTTTAATTAGCCAGGCATGGTGGCACACACCAGTAGTCCCAGCTACTTGAGAGGCTA TTTTTTTGTTTTAATTAGCCAGGCATGGTGGCCCACACCAGTAGTCCCAGCTACTTGAGAGGCTA A C GBF1 Ensembl:ENSG00000107862 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs942740475 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11242449,Human_RBP_ID_17559187 RMVar_hsa_circ_145902,RMVar_hsa_circ_96447,RMVar_hsa_circ_113206,RMVar_hsa_circ_145903,RMVar_hsa_circ_145905,RMVar_hsa_circ_337164,RMVar_hsa_circ_24912 23358 RMVar_ID_23358 Human_SNP_ID_444744139 A-to-I Human chr10 + 102280025 102280025 102280025 ACACACCAGTAGTCCCAGCTACTTGAGAGGCTAAGACAGGAGGATCTCTTGAACCCCAGAAATCA ACACACCAGTAGTCCCAGCTACTTGAGAGGCTGAGACAGGAGGATCTCTTGAACCCCAGAAATCA A G GBF1 Ensembl:ENSG00000107862 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs544018749 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11242450,Human_RBP_ID_17559187 RMVar_hsa_circ_145902,RMVar_hsa_circ_96447,RMVar_hsa_circ_113206,RMVar_hsa_circ_145903,RMVar_hsa_circ_145905,RMVar_hsa_circ_337164,RMVar_hsa_circ_24912 23359 RMVar_ID_23359 Human_SNP_ID_444752221 A-to-I Human chr10 + 102315674 102315674 102315674 TTGTGCTCCTATGAAAATCTAATGTCGTCGCTAATCTGACAGGAGGCAGAGTTTAGGTGGTAATG TTGTGCTCCTATGAAAATCTAATGTCGTCGCTCATCTGACAGGAGGCAGAGTTTAGGTGGTAATG A C GBF1 Ensembl:ENSG00000107862 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1220274574 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_145902,RMVar_hsa_circ_96447,RMVar_hsa_circ_113206,RMVar_hsa_circ_145903,RMVar_hsa_circ_145905,RMVar_hsa_circ_337164,RMVar_hsa_circ_24912 23360 RMVar_ID_23360 Human_SNP_ID_444752222 A-to-I Human chr10 + 102315674 102315674 102315674 TTGTGCTCCTATGAAAATCTAATGTCGTCGCTAATCTGACAGGAGGCAGAGTTTAGGTGGTAATG TTGTGCTCCTATGAAAATCTAATGTCGTCGCTGATCTGACAGGAGGCAGAGTTTAGGTGGTAATG A G GBF1 Ensembl:ENSG00000107862 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1220274574 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_145902,RMVar_hsa_circ_96447,RMVar_hsa_circ_113206,RMVar_hsa_circ_145903,RMVar_hsa_circ_145905,RMVar_hsa_circ_337164,RMVar_hsa_circ_24912 23361 RMVar_ID_23361 Human_SNP_ID_444757737 A-to-I Human chr10 + 102339817 102339817 102339817 AATTTAATTTTTATTTTTTGGAACAGGGTCTTACTCTGTCACCCCAGGCTGGAGTGCAGTGGTAT AATTTAATTTTTATTTTTTGGAACAGGGTCTTGCTCTGTCACCCCAGGCTGGAGTGCAGTGGTAT A G GBF1 Ensembl:ENSG00000107862 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749878009 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_145902,RMVar_hsa_circ_96447,RMVar_hsa_circ_113206,RMVar_hsa_circ_145903,RMVar_hsa_circ_145905,RMVar_hsa_circ_337164,RMVar_hsa_circ_24912 23362 RMVar_ID_23362 Human_SNP_ID_444759151 A-to-I Human chr10 + 102345375 102345375 102345375 TTCTTTTTTCATTTAATGGTATTAACTTGACCAGGCACAGTGGCTCATGCCTGTAATCCCAGCAC TTCTTTTTTCATTTAATGGTATTAACTTGACCGGGCACAGTGGCTCATGCCTGTAATCCCAGCAC A G GBF1 Ensembl:ENSG00000107862 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1480120106 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93134,RMVar_hsa_circ_145902,RMVar_hsa_circ_96447,RMVar_hsa_circ_113206,RMVar_hsa_circ_145903,RMVar_hsa_circ_24912,RMVar_hsa_circ_285552,RMVar_hsa_circ_145908,RMVar_hsa_circ_85087,RMVar_hsa_circ_145909 23363 RMVar_ID_23363 Human_SNP_ID_444759732 A-to-I Human chr10 + 102348175 102348175 102348175 GCCAGGCTGGTCTCGAACTCCTGAGCTCCGGCAATCTGCCCACCTCAGCCTCCCAAAATGCTGGG GCCAGGCTGGTCTCGAACTCCTGAGCTCCGGCTATCTGCCCACCTCAGCCTCCCAAAATGCTGGG A T GBF1 Ensembl:ENSG00000107862 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs534324481 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93134,RMVar_hsa_circ_145902,RMVar_hsa_circ_96447,RMVar_hsa_circ_113206,RMVar_hsa_circ_145903,RMVar_hsa_circ_24912,RMVar_hsa_circ_285552,RMVar_hsa_circ_145908,RMVar_hsa_circ_85087,RMVar_hsa_circ_145909 23364 RMVar_ID_23364 Human_SNP_ID_444759878 A-to-I Human chr10 + 102349041 102349041 102349041 CATGTTAGCACACATCTGTAGTCCTAGCTACTAAGGAGGCTTAGGTAGGAGGATCACTTGAGCCC CATGTTAGCACACATCTGTAGTCCTAGCTACTCAGGAGGCTTAGGTAGGAGGATCACTTGAGCCC A C GBF1 Ensembl:ENSG00000107862 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1478915335 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11243510 RMVar_hsa_circ_93134,RMVar_hsa_circ_145902,RMVar_hsa_circ_96447,RMVar_hsa_circ_113206,RMVar_hsa_circ_145903,RMVar_hsa_circ_24912,RMVar_hsa_circ_285552,RMVar_hsa_circ_145908,RMVar_hsa_circ_85087,RMVar_hsa_circ_145909 23365 RMVar_ID_23365 Human_SNP_ID_444759879 A-to-I Human chr10 + 102349041 102349041 102349041 CATGTTAGCACACATCTGTAGTCCTAGCTACTAAGGAGGCTTAGGTAGGAGGATCACTTGAGCCC CATGTTAGCACACATCTGTAGTCCTAGCTACTGAGGAGGCTTAGGTAGGAGGATCACTTGAGCCC A G GBF1 Ensembl:ENSG00000107862 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1478915335 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11243510 RMVar_hsa_circ_93134,RMVar_hsa_circ_145902,RMVar_hsa_circ_96447,RMVar_hsa_circ_113206,RMVar_hsa_circ_145903,RMVar_hsa_circ_24912,RMVar_hsa_circ_285552,RMVar_hsa_circ_145908,RMVar_hsa_circ_85087,RMVar_hsa_circ_145909 23366 RMVar_ID_23366 Human_SNP_ID_444759933 A-to-I Human chr10 + 102349277 102349277 102349277 AAAATGGGCTGGGCACAGTGGCCCAAGCCTGTAATCCCAGTACTTTGGGAGGCCAAGGTGGGTGA AAAATGGGCTGGGCACAGTGGCCCAAGCCTGTGATCCCAGTACTTTGGGAGGCCAAGGTGGGTGA A G GBF1 Ensembl:ENSG00000107862 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1464713741 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93134,RMVar_hsa_circ_145902,RMVar_hsa_circ_96447,RMVar_hsa_circ_113206,RMVar_hsa_circ_145903,RMVar_hsa_circ_24912,RMVar_hsa_circ_285552,RMVar_hsa_circ_145908,RMVar_hsa_circ_85087,RMVar_hsa_circ_145909 23367 RMVar_ID_23367 Human_SNP_ID_444766477 A-to-I Human chr10 + 102375767 102375767 102375767 CTAGTACCCATAAGTTAAATAGCATGAGGGCAAATAAGCAATGCAGACGGCTGTGAAGCCAGGCT CTAGTACCCATAAGTTAAATAGCATGAGGGCAGATAAGCAATGCAGACGGCTGTGAAGCCAGGCT A G GBF1 Ensembl:ENSG00000107862 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1426398445 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81558,RMVar_hsa_circ_145914,RMVar_hsa_circ_27695,RMVar_hsa_circ_18302,RMVar_hsa_circ_91871,RMVar_hsa_circ_101493,RMVar_hsa_circ_145926,RMVar_hsa_circ_145927,RMVar_hsa_circ_40816,RMVar_hsa_circ_290762,RMVar_hsa_circ_278773,RMVar_hsa_circ_145931,RMVar_hsa_circ_145932 23368 RMVar_ID_23368 Human_SNP_ID_444781777 A-to-I Human chr10 - 102428672 102428672 102428672 GATATGTTGCCGAGGCTGGTCTTAAACTCCTGAGCTCAAACGATCCTCTTGCCTCAGCCTCCCAA GATATGTTGCCGAGGCTGGTCTTAAACTCCTGGGCTCAAACGATCCTCTTGCCTCAGCCTCCCAA T C CUEDC2 Ensembl:ENSG00000107874 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215592051 Functional Loss SNV dbSNP153 33..33 33 - - - 23369 RMVar_ID_23369 Human_SNP_ID_444788571 A-to-I Human chr10 + 102452547 102452547 102452547 CCCACCACACCTGGCTAATTTTTGTATTTTTTAGTAGAAATGGCGTTTCACCATATTGGCCAGAC CCCACCACACCTGGCTAATTTTTGTATTTTTTGGTAGAAATGGCGTTTCACCATATTGGCCAGAC A G RPARP-AS1 Ensembl:ENSG00000269609 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs539199809 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94988,RMVar_hsa_circ_97803,RMVar_hsa_circ_145950,RMVar_hsa_circ_145951 23370 RMVar_ID_23370 Human_SNP_ID_444788577 A-to-I Human chr10 + 102452569 102452569 102452569 TGTATTTTTTAGTAGAAATGGCGTTTCACCATATTGGCCAGACTGGTCTTGAACTCCCAACCCCG TGTATTTTTTAGTAGAAATGGCGTTTCACCATTTTGGCCAGACTGGTCTTGAACTCCCAACCCCG A T RPARP-AS1 Ensembl:ENSG00000269609 lincRNA intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs998294428 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11244014 RMVar_hsa_circ_94988,RMVar_hsa_circ_97803,RMVar_hsa_circ_145950,RMVar_hsa_circ_145951 23371 RMVar_ID_23371 Human_SNP_ID_444788842 A-to-I Human chr10 + 102453663 102453663 102453663 AGGAGGTCAAGCCTGCAGTGAGCTGTGTTCATACCACTGCACTACAGCCTGGGTGGCAGACTGAG AGGAGGTCAAGCCTGCAGTGAGCTGTGTTCATGCCACTGCACTACAGCCTGGGTGGCAGACTGAG A G RPARP-AS1 Ensembl:ENSG00000269609 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1209795122 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94988,RMVar_hsa_circ_97803,RMVar_hsa_circ_145950,RMVar_hsa_circ_145951 23372 RMVar_ID_23372 Human_SNP_ID_444789400 A-to-I Human chr10 + 102455397 102455397 102455397 GCAACCTTGATCTGGGCTCAAGTGATCCTCCTACCTCAGCTTCCTGAGTAGCTAGGACCACAGGT GCAACCTTGATCTGGGCTCAAGTGATCCTCCTGCCTCAGCTTCCTGAGTAGCTAGGACCACAGGT A G RPARP-AS1 Ensembl:ENSG00000269609 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1208662625 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_368688,Human_RBP_ID_1440683,Human_RBP_ID_4104147,Human_RBP_ID_5245931 Human_Splice_Rec_1171726,Human_Splice_Rec_1171732,Human_Splice_Rec_1171740,Human_Splice_Rec_1171748,Human_Splice_Rec_1171752,Human_Splice_Rec_1171754,Human_Splice_Rec_1171756,Human_Splice_Rec_1171758,Human_Splice_Rec_1171759,Human_Splice_Rec_1171762,Human_Splice_Rec_1171766 Human_miRNA_ID_1914311,Human_miRNA_ID_1916762,Human_miRNA_ID_1919211,Human_miRNA_ID_1921668,Human_miRNA_ID_1924124,Human_miRNA_ID_1926576,Human_miRNA_ID_1929026,Human_miRNA_ID_1931479,Human_miRNA_ID_2629308,Human_miRNA_ID_2642420,Human_miRNA_ID_2770595,Human_miRNA_ID_3125160,Human_miRNA_ID_3144883,Human_miRNA_ID_3145028,Human_miRNA_ID_3145173,Human_miRNA_ID_3145318,Human_miRNA_ID_3145462,Human_miRNA_ID_3145606,Human_miRNA_ID_3145750,Human_miRNA_ID_3145896,Human_miRNA_ID_3186853,Human_miRNA_ID_3187578,Human_miRNA_ID_3195117,Human_miRNA_ID_3216581 RMVar_hsa_circ_94988,RMVar_hsa_circ_97803,RMVar_hsa_circ_145950,RMVar_hsa_circ_145951 23373 RMVar_ID_23373 Human_SNP_ID_444793885 A-to-I Human chr10 + 102472485 102472485 102472485 GGGGTTTCGCCATGTTGGCCATGCTGGTCTCAAACTCCTGGCCTTAAGTGATCTGCCTGCCTTGG GGGGTTTCGCCATGTTGGCCATGCTGGTCTCAGACTCCTGGCCTTAAGTGATCTGCCTGCCTTGG A G MFSD13A Ensembl:ENSG00000138111 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1311873863 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66200,RMVar_hsa_circ_87172,RMVar_hsa_circ_93344,RMVar_hsa_circ_145952,RMVar_hsa_circ_353680,RMVar_hsa_circ_145954 23374 RMVar_ID_23374 Human_SNP_ID_444793890 A-to-I Human chr10 + 102472498 102472498 102472498 GTTGGCCATGCTGGTCTCAAACTCCTGGCCTTAAGTGATCTGCCTGCCTTGGCCTCCCAAAGTGC GTTGGCCATGCTGGTCTCAAACTCCTGGCCTTGAGTGATCTGCCTGCCTTGGCCTCCCAAAGTGC A G MFSD13A Ensembl:ENSG00000138111 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1375281096 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66200,RMVar_hsa_circ_87172,RMVar_hsa_circ_93344,RMVar_hsa_circ_145952,RMVar_hsa_circ_353680,RMVar_hsa_circ_145954 23375 RMVar_ID_23375 Human_SNP_ID_444795467 A-to-I Human chr10 - 102478337 102478336 102478337 TCTGCCTTTTTTTTTTTTTTTTTTTTTTTTTGAGATCATGTCTCACTTTGTCACCAGGCTAGAGT TCTGCCTTTTTTTTTTTTTTTTTTTTTTTTTG_GATCATGTCTCACTTTGTCACCAGGCTAGAGT CT C ACTR1A Ensembl:ENSG00000138107 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1564646284 Functional Loss DEL dbSNP153 33..33 33 - - - 23376 RMVar_ID_23376 Human_SNP_ID_444795470 A-to-I Human chr10 - 102478337 102478337 102478337 TCTGCCTTTTTTTTTTTTTTTTTTTTTTTTTGAGATCATGTCTCACTTTGTCACCAGGCTAGAGT TCTGCCTTTTTTTTTTTTTTTTTTTTTTTTTGTGATCATGTCTCACTTTGTCACCAGGCTAGAGT T A ACTR1A Ensembl:ENSG00000138107 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1452931361 Functional Loss SNV dbSNP153 33..33 33 - - - 23377 RMVar_ID_23377 Human_SNP_ID_444797630 A-to-I Human chr10 - 102487233 102487233 102487233 TTTTGTATTTTTTGTAGAGACAAGGTTTTGCCATGTTGCCCAGGCTGGTCTCGAACTCCTGGGTT TTTTGTATTTTTTGTAGAGACAAGGTTTTGCCGTGTTGCCCAGGCTGGTCTCGAACTCCTGGGTT T C ACTR1A Ensembl:ENSG00000138107 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1324268081 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115422,RMVar_hsa_circ_97954,RMVar_hsa_circ_145962,RMVar_hsa_circ_81154,RMVar_hsa_circ_145963,RMVar_hsa_circ_145964,RMVar_hsa_circ_122736,RMVar_hsa_circ_79016,RMVar_hsa_circ_145965,RMVar_hsa_circ_113460,RMVar_hsa_circ_145966,RMVar_hsa_circ_13590,RMVar_hsa_circ_145967,RMVar_hsa_circ_105530,RMVar_hsa_circ_145968 23378 RMVar_ID_23378 Human_SNP_ID_444813664 A-to-I Human chr10 + 102552235 102552235 102552235 GAGAGGCTGAAGCAGGAGGATCACTTGAGCTCAGGAGTTTGAGACCAGCCTGGGCAATGAAGCAA GAGAGGCTGAAGCAGGAGGATCACTTGAGCTCGGGAGTTTGAGACCAGCCTGGGCAATGAAGCAA A G SUFU Ensembl:ENSG00000107882 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1265187050 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_145975,RMVar_hsa_circ_109981 23379 RMVar_ID_23379 Human_SNP_ID_444813671 A-to-I Human chr10 + 102552310 102552310 102552310 ATTAAAGATTAGCCAGGTGTGGTGGCATGCCTATAGTCCCAGCTACTTGGGAGGCTGAGGTAGGA ATTAAAGATTAGCCAGGTGTGGTGGCATGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGTAGGA A G SUFU Ensembl:ENSG00000107882 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs988368376 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_145975,RMVar_hsa_circ_109981 23380 RMVar_ID_23380 Human_SNP_ID_444815982 A-to-I Human chr10 + 102562486 102562486 102562486 CAGAGGTTGCAGTGAGCCGAGATCGCGCCGCTACAGTCTAGCCTGGGCAACAGAGCGAGACTCTG CAGAGGTTGCAGTGAGCCGAGATCGCGCCGCTGCAGTCTAGCCTGGGCAACAGAGCGAGACTCTG A G SUFU Ensembl:ENSG00000107882 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559057886 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_145975,RMVar_hsa_circ_109981 23381 RMVar_ID_23381 Human_SNP_ID_444845775 A-to-I Human chr10 - 102680108 102680108 102680108 AACGCTGTCTCTACTAAAAATACAAAAATATTAGTCGGGCATGGTGGCGGGCGCCTGTAGTCCCA AACGCTGTCTCTACTAAAAATACAAAAATATTTGTCGGGCATGGTGGCGGGCGCCTGTAGTCCCA T A ARL3 Ensembl:ENSG00000138175 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs535359755 Functional Loss SNV dbSNP153 33..33 33 - - - 23382 RMVar_ID_23382 Human_SNP_ID_444846815 A-to-I Human chr10 - 102684750 102684750 102684750 CCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGCAGAATTGCTTGAAGCTGGGAGGCGAAGGTT CCTGTAATCCCAGCTACTTGGGAGGCTGAGGCCGCAGAATTGCTTGAAGCTGGGAGGCGAAGGTT T G ARL3 Ensembl:ENSG00000138175 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs900844441 Functional Loss SNV dbSNP153 33..33 33 - - - 23383 RMVar_ID_23383 Human_SNP_ID_444846829 A-to-I Human chr10 - 102684803 102684803 102684803 CCCCCGTCTCTACTAAAAATACAAAAAAAATCAGCCGGACATGGTGGTGCACACCTGTAATCCCA CCCCCGTCTCTACTAAAAATACAAAAAAAATCCGCCGGACATGGTGGTGCACACCTGTAATCCCA T G ARL3 Ensembl:ENSG00000138175 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1289353842 Functional Loss SNV dbSNP153 33..33 33 - - - 23384 RMVar_ID_23384 Human_SNP_ID_444856977 A-to-I Human chr10 + 102725738 102725738 102725738 AACATAGCGAGGTGCCATCTCTACAAAAAAATACAAAAATTAGCCAGGGTGGTGGTATGTGCCTG AACATAGCGAGGTGCCATCTCTACAAAAAAATGCAAAAATTAGCCAGGGTGGTGGTATGTGCCTG A G SFXN2 Ensembl:ENSG00000156398 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1564741581 Functional Loss SNV dbSNP153 33..33 33 - - - 23385 RMVar_ID_23385 Human_SNP_ID_444856980 A-to-I Human chr10 + 102725772 102725772 102725772 AAAAATTAGCCAGGGTGGTGGTATGTGCCTGTAGTCCCAGTTACTCAGGAGGCTGACCTGGGAGG AAAAATTAGCCAGGGTGGTGGTATGTGCCTGTTGTCCCAGTTACTCAGGAGGCTGACCTGGGAGG A T SFXN2 Ensembl:ENSG00000156398 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1437366751 Functional Loss SNV dbSNP153 33..33 33 - - - 23386 RMVar_ID_23386 Human_SNP_ID_444859732 A-to-I Human chr10 + 102736485 102736485 102736485 CACTCCGTCGCCAGGCTGGGGTGCAGAGGTGCAGTCTCGGCTCACTGCAACCTCCGACTCCCTGA CACTCCGTCGCCAGGCTGGGGTGCAGAGGTGCCGTCTCGGCTCACTGCAACCTCCGACTCCCTGA A C SFXN2 Ensembl:ENSG00000156398 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1472726464 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11485146,Human_RBP_ID_17559192,Human_RBP_ID_24776403 23387 RMVar_ID_23387 Human_SNP_ID_444859766 A-to-I Human chr10 + 102736597 102736597 102736597 TGCCACCACGCACAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGA TGCCACCACGCACAGCTAATTTTTGTATTTTTGGTAGAGACGGGGTTTCACCATGTTGGCCAGGA A G SFXN2 Ensembl:ENSG00000156398 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1349958528 Functional Loss SNV dbSNP153 33..33 33 - - - 23388 RMVar_ID_23388 Human_SNP_ID_444859791 A-to-I Human chr10 + 102736689 102736689 102736689 CGCCCGCCTCAGCCTCCCAAAGTGCTGGCACTACAGGCGTGAGCCACCGCGCCTGGCCTCATTTT CGCCCGCCTCAGCCTCCCAAAGTGCTGGCACTGCAGGCGTGAGCCACCGCGCCTGGCCTCATTTT A G SFXN2 Ensembl:ENSG00000156398 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs577379202 Functional Loss SNV dbSNP153 33..33 33 - - - 23389 RMVar_ID_23389 Human_SNP_ID_444864181 A-to-I Human chr10 + 102755790 102755790 102755790 AATGTTGGCCGGGCGCGGTGGCTCATGCCTGTAATTCCAGCACTTTGGGAGGCCAAGGCAGGTGG AATGTTGGCCGGGCGCGGTGGCTCATGCCTGTGATTCCAGCACTTTGGGAGGCCAAGGCAGGTGG A G WBP1L Ensembl:ENSG00000166272 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1402836542 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_107438 23390 RMVar_ID_23390 Human_SNP_ID_444868674 A-to-I Human chr10 + 102773744 102773744 102773744 GTCTCTACAAAAAATAAAAATTAAAAAAACTTAGCTGAGTGTGGTGGCGTGGTGGCGTGTGCCTG GTCTCTACAAAAAATAAAAATTAAAAAAACTTTGCTGAGTGTGGTGGCGTGGTGGCGTGTGCCTG A T WBP1L Ensembl:ENSG00000166272 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1405935962 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23431168 23391 RMVar_ID_23391 Human_SNP_ID_444876166 A-to-I Human chr10 + 102805531 102805531 102805531 GCAATCCTCTCATCTCAGCCTCCCAAGTAGCTAGGATTTTAGTTGTGAGCCACTGCGCCAAGCAG GCAATCCTCTCATCTCAGCCTCCCAAGTAGCTGGGATTTTAGTTGTGAGCCACTGCGCCAAGCAG A G WBP1L Ensembl:ENSG00000166272 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs886819169 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_313545,RMVar_hsa_circ_145997,RMVar_hsa_circ_77662 23392 RMVar_ID_23392 Human_SNP_ID_444891270 A-to-I Human chr10 + 102863067 102863067 102863067 TAGAAAAGTTCTGTGTTAGGGCCGGGCGCGGTAGCTCACGCCTGTAATCCCAGCACTTTGGGAGG TAGAAAAGTTCTGTGTTAGGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGG A G BORCS7-ASMT,BORCS7 Ensembl:ENSG00000270316,Ensembl:ENSG00000166275 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917178547 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72143 23393 RMVar_ID_23393 Human_SNP_ID_444899303 A-to-I Human chr10 - 102895487 102895487 102895487 GATATCAAGAACTAGAAAGACCCGGGCGTGGTAGTTCACACCTGTAATCCCAGCACTTTGGGAGG GATATCAAGAACTAGAAAGACCCGGGCGTGGTGGTTCACACCTGTAATCCCAGCACTTTGGGAGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs529697614 Functional Loss SNV dbSNP153 33..33 33 - - - 23394 RMVar_ID_23394 Human_SNP_ID_444900620 A-to-I Human chr10 + 102900976 102900976 102900976 GGGCATGGTGGTGCACACCTATAGTCTCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCTTGAA GGGCATGGTGGTGCACACCTATAGTCTCAGCTGCTCGGGAGGCTGAGGCAGGAGAATTGCTTGAA A G BORCS7-ASMT,AS3MT Ensembl:ENSG00000270316,Ensembl:ENSG00000214435 Protein coding,Protein coding 3'UTR,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs934376199 Functional Loss SNV dbSNP153 33..33 33 - - - 23395 RMVar_ID_23395 Human_SNP_ID_444900625 A-to-I Human chr10 + 102900998 102900998 102900998 AGTCTCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCTTGAACCCAGGAAGTAGAGGCTGCAGT AGTCTCAGCTACTCGGGAGGCTGAGGCAGGAGCATTGCTTGAACCCAGGAAGTAGAGGCTGCAGT A C BORCS7-ASMT,AS3MT Ensembl:ENSG00000270316,Ensembl:ENSG00000214435 Protein coding,Protein coding 3'UTR,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1325720958 Functional Loss SNV dbSNP153 33..33 33 - - - 23396 RMVar_ID_23396 Human_SNP_ID_444900731 A-to-I Human chr10 + 102901319 102901319 102901319 GGGTTCACGCCATTCTCCTGCCTCAGACTCCCAAGTAGCTGGGACTACAGGCACCTACCACCATG GGGTTCACGCCATTCTCCTGCCTCAGACTCCCCAGTAGCTGGGACTACAGGCACCTACCACCATG A C BORCS7-ASMT,AS3MT Ensembl:ENSG00000270316,Ensembl:ENSG00000214435 Protein coding,Protein coding 3'UTR,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1030338288 Functional Loss SNV dbSNP153 33..33 33 - - - 23397 RMVar_ID_23397 Human_SNP_ID_444900734 A-to-I Human chr10 + 102901333 102901333 102901333 CTCCTGCCTCAGACTCCCAAGTAGCTGGGACTACAGGCACCTACCACCATGCCCAGCTAATTTTT CTCCTGCCTCAGACTCCCAAGTAGCTGGGACTGCAGGCACCTACCACCATGCCCAGCTAATTTTT A G BORCS7-ASMT,AS3MT Ensembl:ENSG00000270316,Ensembl:ENSG00000214435 Protein coding,Protein coding 3'UTR,3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs986205008 Functional Loss SNV dbSNP153 33..33 33 - - - 23398 RMVar_ID_23398 Human_SNP_ID_444900736 A-to-I Human chr10 + 102901359 102901338 102901359 GGGACTACAGGCACCTACCACCATGCCCAGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTC GGGACTACAGGC_____________________ATTTTTTGTATTTTTAGTAGAGACGGGGTTTC CACCTACCACCATGCCCAGCTA C BORCS7-ASMT,AS3MT Ensembl:ENSG00000270316,Ensembl:ENSG00000214435 Protein coding,Protein coding 3'UTR,3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1316910598 Functional Loss DEL dbSNP153 13..33 33 - - - 23399 RMVar_ID_23399 Human_SNP_ID_444900769 A-to-I Human chr10 + 102901454 102901454 102901454 TGACCTCGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAAGCATGAGCCACTGCGC TGACCTCGTGATCCGCCCGCCTCGGCCTCCCACAGTGCTGGGATTACAAGCATGAGCCACTGCGC A C BORCS7-ASMT,AS3MT Ensembl:ENSG00000270316,Ensembl:ENSG00000214435 Protein coding,Protein coding 3'UTR,3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1299435575 Functional Loss SNV dbSNP153 33..33 33 - - - 23400 RMVar_ID_23400 Human_SNP_ID_444907082 A-to-I Human chr10 + 102926815 102926815 102926815 TCGGCTCACTGCAAGCTCCACCTCCTGGGCTCATGCCATTCTCATGCCTCAGCTTCCCGAGAAGC TCGGCTCACTGCAAGCTCCACCTCCTGGGCTCCTGCCATTCTCATGCCTCAGCTTCCCGAGAAGC A C CNNM2 Ensembl:ENSG00000148842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1263389276 Functional Loss SNV dbSNP153 33..33 33 - - - 23401 RMVar_ID_23401 Human_SNP_ID_444907274 A-to-I Human chr10 + 102927607 102927607 102927607 CACCATGGTGAAACCCCGTTTCTAATAAAAATACAGAAAAATTAGCTGTGCGTGGTGGTGGGTGC CACCATGGTGAAACCCCGTTTCTAATAAAAATGCAGAAAAATTAGCTGTGCGTGGTGGTGGGTGC A G CNNM2 Ensembl:ENSG00000148842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1469212395 Functional Loss SNV dbSNP153 33..33 33 - - - 23402 RMVar_ID_23402 Human_SNP_ID_444907300 A-to-I Human chr10 + 102927735 102927735 102927735 TGCCGTGAGCTGAGATCACGTCACTGGACGACAAAGTGAGACTCTGTCTCAAAAAAAAAGGAGGG TGCCGTGAGCTGAGATCACGTCACTGGACGACGAAGTGAGACTCTGTCTCAAAAAAAAAGGAGGG A G CNNM2 Ensembl:ENSG00000148842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1460664669 Functional Loss SNV dbSNP153 33..33 33 - - - 23403 RMVar_ID_23403 Human_SNP_ID_444907301 A-to-I Human chr10 + 102927736 102927736 102927736 GCCGTGAGCTGAGATCACGTCACTGGACGACAAAGTGAGACTCTGTCTCAAAAAAAAAGGAGGGG GCCGTGAGCTGAGATCACGTCACTGGACGACACAGTGAGACTCTGTCTCAAAAAAAAAGGAGGGG A C CNNM2 Ensembl:ENSG00000148842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1321538856 Functional Loss SNV dbSNP153 33..33 33 - - - 23404 RMVar_ID_23404 Human_SNP_ID_444908188 A-to-I Human chr10 + 102931412 102931412 102931412 CAGTTTCACTCTTGTTGCCCAGGCTGTAGTGCAATGGTGCGATCTCACCTCACCGCAACCTCCGC CAGTTTCACTCTTGTTGCCCAGGCTGTAGTGCGATGGTGCGATCTCACCTCACCGCAACCTCCGC A G CNNM2 Ensembl:ENSG00000148842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1295076717 Functional Loss SNV dbSNP153 33..33 33 - - - 23405 RMVar_ID_23405 Human_SNP_ID_444909768 A-to-I Human chr10 + 102937886 102937886 102937886 GGCTCAAACAATCCTCCCACCTTGGCTTCCCAAAGTGTTGGGAGTATAGGCATGAGCCACTGCAC GGCTCAAACAATCCTCCCACCTTGGCTTCCCAGAGTGTTGGGAGTATAGGCATGAGCCACTGCAC A G CNNM2 Ensembl:ENSG00000148842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1364478425 Functional Loss SNV dbSNP153 33..33 33 - - - 23406 RMVar_ID_23406 Human_SNP_ID_444911251 A-to-I Human chr10 + 102944158 102944158 102944158 CAGGCAAGACTGGTGCGATCTCGGCTCACTGCAGTCTCCGCCTCCTGGGTTCAAGCAATTCTCCT CAGGCAAGACTGGTGCGATCTCGGCTCACTGCGGTCTCCGCCTCCTGGGTTCAAGCAATTCTCCT A G CNNM2 Ensembl:ENSG00000148842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1019285942 Functional Loss SNV dbSNP153 33..33 33 - - - 23407 RMVar_ID_23407 Human_SNP_ID_444912801 A-to-I Human chr10 + 102950703 102950703 102950703 TTAAGCCCAGGAATTCAAGGTTGTATAGAGCTATGATTAAACCAGTACACTCCAGCCTGGACAAC TTAAGCCCAGGAATTCAAGGTTGTATAGAGCTGTGATTAAACCAGTACACTCCAGCCTGGACAAC A G CNNM2 Ensembl:ENSG00000148842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1442268541 Functional Loss SNV dbSNP153 33..33 33 - - - 23408 RMVar_ID_23408 Human_SNP_ID_444914898 A-to-I Human chr10 + 102959600 102959600 102959600 TCCTCATCTTTTTGTTTGTTTGCTTTAGAGACAGGGTCTTGCTCTGTCACCCAAGCTGGGGTGCA TCCTCATCTTTTTGTTTGTTTGCTTTAGAGACTGGGTCTTGCTCTGTCACCCAAGCTGGGGTGCA A T CNNM2 Ensembl:ENSG00000148842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334228721 Functional Loss SNV dbSNP153 33..33 33 - - - 23409 RMVar_ID_23409 Human_SNP_ID_444917401 A-to-I Human chr10 + 102970173 102970173 102970173 ATGGTCGAAAGTAAAAGAATACTATTTTAGCCAGGTGTGGTGGTGCATACTTATGGTCCCAGCTA ATGGTCGAAAGTAAAAGAATACTATTTTAGCCGGGTGTGGTGGTGCATACTTATGGTCCCAGCTA A G CNNM2 Ensembl:ENSG00000148842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928952137 Functional Loss SNV dbSNP153 33..33 33 - - - 23410 RMVar_ID_23410 Human_SNP_ID_444924758 A-to-I Human chr10 + 103000113 103000113 103000113 CAAAAATTAGTTGGGTGTGGTGGCAGGCACCTATAATACCAGCTACTTGGGAGGCTGAGGCAGGA CAAAAATTAGTTGGGTGTGGTGGCAGGCACCTGTAATACCAGCTACTTGGGAGGCTGAGGCAGGA A G CNNM2 Ensembl:ENSG00000148842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs955054432 Functional Loss SNV dbSNP153 33..33 33 - - - 23411 RMVar_ID_23411 Human_SNP_ID_444946606 A-to-I Human chr10 - 103088526 103088526 103088526 AAAATTACCTGGGCGTGGTGGTGCATGCCTGTAATCCCATCATCTACTCAGGAGGCTGAGGCAGG AAAATTACCTGGGCGTGGTGGTGCATGCCTGTCATCCCATCATCTACTCAGGAGGCTGAGGCAGG T G NT5C2 Ensembl:ENSG00000076685 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1358435921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_368967,Human_RBP_ID_981250,Human_RBP_ID_17225290,Human_RBP_ID_17457499,Human_RBP_ID_17768504 RMVar_hsa_circ_146018,RMVar_hsa_circ_84668 23412 RMVar_ID_23412 Human_SNP_ID_444953544 A-to-I Human chr10 - 103117587 103117587 103117587 GCTGCAGCACAGTGGTGCAATTGTAGTTTACTATAACCTTGAACTACTGGGCTCAAGTGATCCTC GCTGCAGCACAGTGGTGCAATTGTAGTTTACTCTAACCTTGAACTACTGGGCTCAAGTGATCCTC T G NT5C2 Ensembl:ENSG00000076685 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1423611420 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109953,RMVar_hsa_circ_146021,RMVar_hsa_circ_26858,RMVar_hsa_circ_64491,RMVar_hsa_circ_343970,RMVar_hsa_circ_146029,RMVar_hsa_circ_146031,RMVar_hsa_circ_87429,RMVar_hsa_circ_316578,RMVar_hsa_circ_146030,RMVar_hsa_circ_335269,RMVar_hsa_circ_323188 23413 RMVar_ID_23413 Human_SNP_ID_444958421 A-to-I Human chr10 - 103136040 103136040 103136040 CTCTGTCTCCCAGGCTGGAGTGCAATGGTGCAATCCTGGCTCACTGCAACCTGTGCCTCCCAGGT CTCTGTCTCCCAGGCTGGAGTGCAATGGTGCAGTCCTGGCTCACTGCAACCTGTGCCTCCCAGGT T C NT5C2 Ensembl:ENSG00000076685 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1045785714 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109953,RMVar_hsa_circ_146021,RMVar_hsa_circ_26858,RMVar_hsa_circ_64491,RMVar_hsa_circ_343970,RMVar_hsa_circ_146029,RMVar_hsa_circ_146031,RMVar_hsa_circ_87429,RMVar_hsa_circ_316578,RMVar_hsa_circ_146030,RMVar_hsa_circ_335269,RMVar_hsa_circ_323188 23414 RMVar_ID_23414 Human_SNP_ID_444958629 A-to-I Human chr10 - 103136789 103136789 103136789 AAACCCCATCTCTACTAAAAAATACAAAAATTAGTTGGGTGTGGTGGTACGTGCCTGTAGTCTCA AAACCCCATCTCTACTAAAAAATACAAAAATTTGTTGGGTGTGGTGGTACGTGCCTGTAGTCTCA T A NT5C2 Ensembl:ENSG00000076685 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs940044913 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2187420 RMVar_hsa_circ_109953,RMVar_hsa_circ_146021,RMVar_hsa_circ_26858,RMVar_hsa_circ_64491,RMVar_hsa_circ_343970,RMVar_hsa_circ_146029,RMVar_hsa_circ_146031,RMVar_hsa_circ_87429,RMVar_hsa_circ_316578,RMVar_hsa_circ_146030,RMVar_hsa_circ_335269,RMVar_hsa_circ_319725,RMVar_hsa_circ_323188,RMVar_hsa_circ_322332 23415 RMVar_ID_23415 Human_SNP_ID_444960386 A-to-I Human chr10 - 103143949 103143949 103143949 TGGAGGGTGTTTTTTGTTTCTTTGTTTGAGACAGGGTCTTGCTCTGTTGCCCAGGCTAGAATGCA TGGAGGGTGTTTTTTGTTTCTTTGTTTGAGACGGGGTCTTGCTCTGTTGCCCAGGCTAGAATGCA T C NT5C2 Ensembl:ENSG00000076685 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1305976696 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109953,RMVar_hsa_circ_146021,RMVar_hsa_circ_64491,RMVar_hsa_circ_343970,RMVar_hsa_circ_146029,RMVar_hsa_circ_146031,RMVar_hsa_circ_316578,RMVar_hsa_circ_335269,RMVar_hsa_circ_291695,RMVar_hsa_circ_323188,RMVar_hsa_circ_322332,RMVar_hsa_circ_294408,RMVar_hsa_circ_146032,RMVar_hsa_circ_146033 23416 RMVar_ID_23416 Human_SNP_ID_444963873 A-to-I Human chr10 - 103159597 103159597 103159597 TCACCCAAGGTGTAGTACAGTGACATGATCATAGCTCACTGTAACCCTGAACTCCTGGCTTCACG TCACCCAAGGTGTAGTACAGTGACATGATCATGGCTCACTGTAACCCTGAACTCCTGGCTTCACG T C NT5C2 Ensembl:ENSG00000076685 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs865776221 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11247953 RMVar_hsa_circ_109953,RMVar_hsa_circ_146021,RMVar_hsa_circ_64491,RMVar_hsa_circ_343970,RMVar_hsa_circ_146029,RMVar_hsa_circ_146031,RMVar_hsa_circ_316578,RMVar_hsa_circ_335269,RMVar_hsa_circ_291695,RMVar_hsa_circ_323188,RMVar_hsa_circ_322332,RMVar_hsa_circ_294408,RMVar_hsa_circ_146032,RMVar_hsa_circ_146033 23417 RMVar_ID_23417 Human_SNP_ID_444963874 A-to-I Human chr10 - 103159597 103159597 103159597 TCACCCAAGGTGTAGTACAGTGACATGATCATAGCTCACTGTAACCCTGAACTCCTGGCTTCACG TCACCCAAGGTGTAGTACAGTGACATGATCATCGCTCACTGTAACCCTGAACTCCTGGCTTCACG T G NT5C2 Ensembl:ENSG00000076685 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs865776221 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11247953 RMVar_hsa_circ_109953,RMVar_hsa_circ_146021,RMVar_hsa_circ_64491,RMVar_hsa_circ_343970,RMVar_hsa_circ_146029,RMVar_hsa_circ_146031,RMVar_hsa_circ_316578,RMVar_hsa_circ_335269,RMVar_hsa_circ_291695,RMVar_hsa_circ_323188,RMVar_hsa_circ_322332,RMVar_hsa_circ_294408,RMVar_hsa_circ_146032,RMVar_hsa_circ_146033 23418 RMVar_ID_23418 Human_SNP_ID_444964293 A-to-I Human chr10 - 103161377 103161377 103161377 TACCAGGAGTTTGAGACTAGCCTGGGCAACATAGCAAAACCCCATCTCTACAGAAAATACATAAA TACCAGGAGTTTGAGACTAGCCTGGGCAACATGGCAAAACCCCATCTCTACAGAAAATACATAAA T C NT5C2 Ensembl:ENSG00000076685 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1052012795 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109953,RMVar_hsa_circ_146021,RMVar_hsa_circ_64491,RMVar_hsa_circ_343970,RMVar_hsa_circ_146029,RMVar_hsa_circ_146031,RMVar_hsa_circ_316578,RMVar_hsa_circ_335269,RMVar_hsa_circ_291695,RMVar_hsa_circ_323188,RMVar_hsa_circ_322332,RMVar_hsa_circ_294408,RMVar_hsa_circ_146032,RMVar_hsa_circ_146033 23419 RMVar_ID_23419 Human_SNP_ID_444964366 A-to-I Human chr10 - 103161688 103161688 103161688 TTGGAGTCTTACTCTGTCATCCAGGCTGGAGTACAGTGGCGCAGTCATAGCTCACAGAAGCCTCA TTGGAGTCTTACTCTGTCATCCAGGCTGGAGTGCAGTGGCGCAGTCATAGCTCACAGAAGCCTCA T C NT5C2 Ensembl:ENSG00000076685 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1186415373 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11247980 RMVar_hsa_circ_109953,RMVar_hsa_circ_146021,RMVar_hsa_circ_64491,RMVar_hsa_circ_343970,RMVar_hsa_circ_146029,RMVar_hsa_circ_146031,RMVar_hsa_circ_316578,RMVar_hsa_circ_335269,RMVar_hsa_circ_291695,RMVar_hsa_circ_323188,RMVar_hsa_circ_322332,RMVar_hsa_circ_294408,RMVar_hsa_circ_146032,RMVar_hsa_circ_146033 23420 RMVar_ID_23420 Human_SNP_ID_444964522 A-to-I Human chr10 - 103162289 103162289 103162289 GCAGCTTCAGTGGGGCGTGGTGGCTCATGCCTATAATCCTAGGACTTTGGGAGGCCGAGGTGGGT GCAGCTTCAGTGGGGCGTGGTGGCTCATGCCTGTAATCCTAGGACTTTGGGAGGCCGAGGTGGGT T C NT5C2 Ensembl:ENSG00000076685 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1207612976 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109953,RMVar_hsa_circ_146021,RMVar_hsa_circ_64491,RMVar_hsa_circ_343970,RMVar_hsa_circ_146029,RMVar_hsa_circ_146031,RMVar_hsa_circ_316578,RMVar_hsa_circ_335269,RMVar_hsa_circ_291695,RMVar_hsa_circ_323188,RMVar_hsa_circ_322332,RMVar_hsa_circ_294408,RMVar_hsa_circ_146032,RMVar_hsa_circ_146033 23421 RMVar_ID_23421 Human_SNP_ID_444965044 A-to-I Human chr10 - 103164129 103164129 103164129 GTGATCCTCCCAACTCAGCCTTCCAAGCAGCTAGAAATACAGGAGCACACCACCACACCTAGCTA GTGATCCTCCCAACTCAGCCTTCCAAGCAGCTGGAAATACAGGAGCACACCACCACACCTAGCTA T C NT5C2 Ensembl:ENSG00000076685 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1457378803 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109953,RMVar_hsa_circ_146021,RMVar_hsa_circ_64491,RMVar_hsa_circ_343970,RMVar_hsa_circ_146029,RMVar_hsa_circ_146031,RMVar_hsa_circ_316578,RMVar_hsa_circ_335269,RMVar_hsa_circ_291695,RMVar_hsa_circ_323188,RMVar_hsa_circ_322332,RMVar_hsa_circ_294408,RMVar_hsa_circ_146032,RMVar_hsa_circ_146033 23422 RMVar_ID_23422 Human_SNP_ID_444965102 A-to-I Human chr10 - 103164325 103164314 103164325 TGAACCCAGGAGGCAGAAGTTGCAGTGAGCCAAGATTGAGCCAGTGCACTCCAGCCTGGCGACAG TGAACCCAGGAGGCAGAAGTTGCAGTGAGCCA___________GTGCACTCCAGCCTGGCGACAG CTGGCTCAATCT C NT5C2 Ensembl:ENSG00000076685 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1194679425 Functional Loss DEL dbSNP153 33..43 33 - - - RMVar_hsa_circ_109953,RMVar_hsa_circ_146021,RMVar_hsa_circ_64491,RMVar_hsa_circ_343970,RMVar_hsa_circ_146029,RMVar_hsa_circ_146031,RMVar_hsa_circ_316578,RMVar_hsa_circ_335269,RMVar_hsa_circ_291695,RMVar_hsa_circ_323188,RMVar_hsa_circ_322332,RMVar_hsa_circ_294408,RMVar_hsa_circ_146032,RMVar_hsa_circ_146033 23423 RMVar_ID_23423 Human_SNP_ID_444965755 A-to-I Human chr10 - 103166926 103166926 103166926 AACTGTGGCTGGGTGTGGTGGCTTACACCTATAATACTAGCACTTTGAGAGACCGAGATGGGAAG AACTGTGGCTGGGTGTGGTGGCTTACACCTATCATACTAGCACTTTGAGAGACCGAGATGGGAAG T G NT5C2 Ensembl:ENSG00000076685 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1173185291 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17768529,Human_RBP_ID_18585981 RMVar_hsa_circ_109953,RMVar_hsa_circ_146021,RMVar_hsa_circ_64491,RMVar_hsa_circ_343970,RMVar_hsa_circ_146029,RMVar_hsa_circ_146031,RMVar_hsa_circ_316578,RMVar_hsa_circ_335269,RMVar_hsa_circ_291695,RMVar_hsa_circ_323188,RMVar_hsa_circ_322332,RMVar_hsa_circ_294408,RMVar_hsa_circ_146032,RMVar_hsa_circ_146033 23424 RMVar_ID_23424 Human_SNP_ID_444965756 A-to-I Human chr10 - 103166928 103166928 103166928 AAAACTGTGGCTGGGTGTGGTGGCTTACACCTATAATACTAGCACTTTGAGAGACCGAGATGGGA AAAACTGTGGCTGGGTGTGGTGGCTTACACCTGTAATACTAGCACTTTGAGAGACCGAGATGGGA T C NT5C2 Ensembl:ENSG00000076685 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs578108983 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17768529,Human_RBP_ID_18585981 RMVar_hsa_circ_109953,RMVar_hsa_circ_146021,RMVar_hsa_circ_64491,RMVar_hsa_circ_343970,RMVar_hsa_circ_146029,RMVar_hsa_circ_146031,RMVar_hsa_circ_316578,RMVar_hsa_circ_335269,RMVar_hsa_circ_291695,RMVar_hsa_circ_323188,RMVar_hsa_circ_322332,RMVar_hsa_circ_294408,RMVar_hsa_circ_146032,RMVar_hsa_circ_146033 23425 RMVar_ID_23425 Human_SNP_ID_444966362 A-to-I Human chr10 - 103169360 103169360 103169360 CTCCTGCCTTGTCCTTCCAAAGTGCTGGGATTACAAGTGTGAGCCACCATGCCCCGTGTTTAAAA CTCCTGCCTTGTCCTTCCAAAGTGCTGGGATTGCAAGTGTGAGCCACCATGCCCCGTGTTTAAAA T C NT5C2 Ensembl:ENSG00000076685 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1372131480 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11248067 Human_Splice_Rec_1172676 RMVar_hsa_circ_109953,RMVar_hsa_circ_146021,RMVar_hsa_circ_64491,RMVar_hsa_circ_343970,RMVar_hsa_circ_146029,RMVar_hsa_circ_146031,RMVar_hsa_circ_316578,RMVar_hsa_circ_335269,RMVar_hsa_circ_291695,RMVar_hsa_circ_323188,RMVar_hsa_circ_322332,RMVar_hsa_circ_294408,RMVar_hsa_circ_146032,RMVar_hsa_circ_146033 23426 RMVar_ID_23426 Human_SNP_ID_444966372 A-to-I Human chr10 - 103169425 103169425 103169425 TTTTGTAGAGACAAAGTCTTGCTGTGTTACCCAGGTTGATCTTGAACTCTTGTTCTCAAGTGATC TTTTGTAGAGACAAAGTCTTGCTGTGTTACCCGGGTTGATCTTGAACTCTTGTTCTCAAGTGATC T C NT5C2 Ensembl:ENSG00000076685 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1445425624 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11248068 Human_Splice_Rec_1172676 RMVar_hsa_circ_109953,RMVar_hsa_circ_146021,RMVar_hsa_circ_64491,RMVar_hsa_circ_343970,RMVar_hsa_circ_146029,RMVar_hsa_circ_146031,RMVar_hsa_circ_316578,RMVar_hsa_circ_335269,RMVar_hsa_circ_291695,RMVar_hsa_circ_323188,RMVar_hsa_circ_322332,RMVar_hsa_circ_294408,RMVar_hsa_circ_146032,RMVar_hsa_circ_146033 23427 RMVar_ID_23427 Human_SNP_ID_444966459 A-to-I Human chr10 - 103169788 103169788 103169788 TTTCTAGAGATGTGGTCTCACTATGTTGTCCAAGCTGGTTTTGATCTTCTGGCTGCAAGCAGTCC TTTCTAGAGATGTGGTCTCACTATGTTGTCCAGGCTGGTTTTGATCTTCTGGCTGCAAGCAGTCC T C NT5C2 Ensembl:ENSG00000076685 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1468435945 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2187673 RMVar_hsa_circ_109953,RMVar_hsa_circ_146021,RMVar_hsa_circ_64491,RMVar_hsa_circ_343970,RMVar_hsa_circ_146029,RMVar_hsa_circ_146031,RMVar_hsa_circ_316578,RMVar_hsa_circ_335269,RMVar_hsa_circ_291695,RMVar_hsa_circ_323188,RMVar_hsa_circ_322332,RMVar_hsa_circ_294408,RMVar_hsa_circ_146032,RMVar_hsa_circ_146033 23428 RMVar_ID_23428 Human_SNP_ID_444966725 A-to-I Human chr10 - 103170687 103170687 103170687 CCCTGTCTCTACAAAAAAAAAACATAAAAATTAGCCAGGTGTGGTGGCTTACGCCTGTGGACTCA CCCTGTCTCTACAAAAAAAAAACATAAAAATTTGCCAGGTGTGGTGGCTTACGCCTGTGGACTCA T A NT5C2 Ensembl:ENSG00000076685 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1287755236 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23431573 RMVar_hsa_circ_109953,RMVar_hsa_circ_146021,RMVar_hsa_circ_64491,RMVar_hsa_circ_343970,RMVar_hsa_circ_146029,RMVar_hsa_circ_146031,RMVar_hsa_circ_316578,RMVar_hsa_circ_335269,RMVar_hsa_circ_291695,RMVar_hsa_circ_323188,RMVar_hsa_circ_322332,RMVar_hsa_circ_294408,RMVar_hsa_circ_146032,RMVar_hsa_circ_146033 23429 RMVar_ID_23429 Human_SNP_ID_444967030 A-to-I Human chr10 - 103172044 103172044 103172044 CACCACACCTGGCTAATTTTTTAATTTTTAGTAGAGACAGGGTTTCACCGTGTTTGCCAGGCTGG CACCACACCTGGCTAATTTTTTAATTTTTAGTGGAGACAGGGTTTCACCGTGTTTGCCAGGCTGG T C NT5C2 Ensembl:ENSG00000076685 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1398562019 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109953,RMVar_hsa_circ_146021,RMVar_hsa_circ_64491,RMVar_hsa_circ_343970,RMVar_hsa_circ_146029,RMVar_hsa_circ_146031,RMVar_hsa_circ_316578,RMVar_hsa_circ_335269,RMVar_hsa_circ_291695,RMVar_hsa_circ_323188,RMVar_hsa_circ_322332,RMVar_hsa_circ_294408,RMVar_hsa_circ_146032,RMVar_hsa_circ_146033 23430 RMVar_ID_23430 Human_SNP_ID_444967064 A-to-I Human chr10 - 103172134 103172134 103172134 GCGGTCTCAGCTCACTGCAACCTCTGCCTCCCAGGTTCAAGCGATTCTCCTGCCTCACCGTCCCG GCGGTCTCAGCTCACTGCAACCTCTGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCACCGTCCCG T C NT5C2 Ensembl:ENSG00000076685 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1163239 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109953,RMVar_hsa_circ_146021,RMVar_hsa_circ_64491,RMVar_hsa_circ_343970,RMVar_hsa_circ_146029,RMVar_hsa_circ_146031,RMVar_hsa_circ_316578,RMVar_hsa_circ_335269,RMVar_hsa_circ_291695,RMVar_hsa_circ_323188,RMVar_hsa_circ_322332,RMVar_hsa_circ_294408,RMVar_hsa_circ_146032,RMVar_hsa_circ_146033 23431 RMVar_ID_23431 Human_SNP_ID_444967082 A-to-I Human chr10 - 103172199 103172199 103172199 TATTTAAATTTTTGTTTTTTATTTTTTGAGACAGAGTCTTTGCTCTTGTCTCTCAGTACAGTGGC TATTTAAATTTTTGTTTTTTATTTTTTGAGACGGAGTCTTTGCTCTTGTCTCTCAGTACAGTGGC T C NT5C2 Ensembl:ENSG00000076685 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1484040377 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2187700,Human_RBP_ID_11248103 RMVar_hsa_circ_109953,RMVar_hsa_circ_146021,RMVar_hsa_circ_64491,RMVar_hsa_circ_343970,RMVar_hsa_circ_146029,RMVar_hsa_circ_146031,RMVar_hsa_circ_316578,RMVar_hsa_circ_335269,RMVar_hsa_circ_291695,RMVar_hsa_circ_323188,RMVar_hsa_circ_322332,RMVar_hsa_circ_294408,RMVar_hsa_circ_146032,RMVar_hsa_circ_146033 23432 RMVar_ID_23432 Human_SNP_ID_444967216 A-to-I Human chr10 - 103172673 103172673 103172673 GGCCACCATGCCCAGCTAATTTTTGTAATTTTAGTAGAGATGGAGTTTCGCCATGTTGGCCAGGC GGCCACCATGCCCAGCTAATTTTTGTAATTTTGGTAGAGATGGAGTTTCGCCATGTTGGCCAGGC T C NT5C2 Ensembl:ENSG00000076685 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs534708375 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109953,RMVar_hsa_circ_146021,RMVar_hsa_circ_64491,RMVar_hsa_circ_343970,RMVar_hsa_circ_146029,RMVar_hsa_circ_146031,RMVar_hsa_circ_316578,RMVar_hsa_circ_335269,RMVar_hsa_circ_291695,RMVar_hsa_circ_323188,RMVar_hsa_circ_322332,RMVar_hsa_circ_294408,RMVar_hsa_circ_146032,RMVar_hsa_circ_146033 23433 RMVar_ID_23433 Human_SNP_ID_444968696 A-to-I Human chr10 - 103178417 103178417 103178417 CCTCAGCCTCCCAAGTAGCTGGGACTACAGATACGGACCACCATGCCCAACTAATTTTTGTATAT CCTCAGCCTCCCAAGTAGCTGGGACTACAGATTCGGACCACCATGCCCAACTAATTTTTGTATAT T A NT5C2 Ensembl:ENSG00000076685 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1390208384 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_291695,RMVar_hsa_circ_146033,RMVar_hsa_circ_146035 23434 RMVar_ID_23434 Human_SNP_ID_444968697 A-to-I Human chr10 - 103178423 103178423 103178423 CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGATACGGACCACCATGCCCAACTAATTTTT CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTGCAGATACGGACCACCATGCCCAACTAATTTTT T C NT5C2 Ensembl:ENSG00000076685 Protein coding intron GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs572640856 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_291695,RMVar_hsa_circ_146033,RMVar_hsa_circ_146035 23435 RMVar_ID_23435 Human_SNP_ID_444986075 A-to-I Human chr10 + 103246303 103246303 103246303 CCTTTCATCTCGAGGCTACTGAGAACCCAGGGACTTTGATTAAAGACATTCGGGAGAATGGGATG CCTTTCATCTCGAGGCTACTGAGAACCCAGGGGCTTTGATTAAAGACATTCGGGAGAATGGGATG A G RPEL1 Ensembl:ENSG00000235376 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs766118089 Functional Loss SNV dbSNP153 33..33 33 - - - 23436 RMVar_ID_23436 Human_SNP_ID_445004958 A-to-I Human chr10 - 103320818 103320818 103320818 GTGCATGGTTTACAGATATGTGACCTTCATTTATGGTTATTTACTAACAGGAACGAGTAATTCCC GTGCATGGTTTACAGATATGTGACCTTCATTTTTGGTTATTTACTAACAGGAACGAGTAATTCCC T A PCGF6 Ensembl:ENSG00000156374 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7093667 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2248,GWAS_ID_2249,GWAS_ID_2250,GWAS_ID_2251,GWAS_ID_2252,GWAS_ID_2253,GWAS_ID_2254,GWAS_ID_2255,GWAS_ID_2256,GWAS_ID_2257,GWAS_ID_2258,GWAS_ID_2259,GWAS_ID_2260,GWAS_ID_2261,GWAS_ID_2262,GWAS_ID_2263,GWAS_ID_2264,GWAS_ID_2265,GWAS_ID_2266,GWAS_ID_2267,GWAS_ID_2268,GWAS_ID_2269,GWAS_ID_2270,GWAS_ID_2271,GWAS_ID_2272,GWAS_ID_2273,GWAS_ID_2274,GWAS_ID_2275,GWAS_ID_2276,GWAS_ID_2277,GWAS_ID_2278,GWAS_ID_2279,GWAS_ID_2280,GWAS_ID_2281,GWAS_ID_2282 RMVar_hsa_circ_70813,RMVar_hsa_circ_96751,RMVar_hsa_circ_124980,RMVar_hsa_circ_112774,RMVar_hsa_circ_146039,RMVar_hsa_circ_146040,RMVar_hsa_circ_340038,RMVar_hsa_circ_370695,RMVar_hsa_circ_311081,RMVar_hsa_circ_88319,RMVar_hsa_circ_146041,RMVar_hsa_circ_146043,RMVar_hsa_circ_146044,RMVar_hsa_circ_146042 23437 RMVar_ID_23437 Human_SNP_ID_445004959 A-to-I Human chr10 - 103320818 103320818 103320818 GTGCATGGTTTACAGATATGTGACCTTCATTTATGGTTATTTACTAACAGGAACGAGTAATTCCC GTGCATGGTTTACAGATATGTGACCTTCATTTGTGGTTATTTACTAACAGGAACGAGTAATTCCC T C PCGF6 Ensembl:ENSG00000156374 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7093667 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2248,GWAS_ID_2249,GWAS_ID_2250,GWAS_ID_2251,GWAS_ID_2252,GWAS_ID_2253,GWAS_ID_2254,GWAS_ID_2255,GWAS_ID_2256,GWAS_ID_2257,GWAS_ID_2258,GWAS_ID_2259,GWAS_ID_2260,GWAS_ID_2261,GWAS_ID_2262,GWAS_ID_2263,GWAS_ID_2264,GWAS_ID_2265,GWAS_ID_2266,GWAS_ID_2267,GWAS_ID_2268,GWAS_ID_2269,GWAS_ID_2270,GWAS_ID_2271,GWAS_ID_2272,GWAS_ID_2273,GWAS_ID_2274,GWAS_ID_2275,GWAS_ID_2276,GWAS_ID_2277,GWAS_ID_2278,GWAS_ID_2279,GWAS_ID_2280,GWAS_ID_2281,GWAS_ID_2282 RMVar_hsa_circ_70813,RMVar_hsa_circ_96751,RMVar_hsa_circ_124980,RMVar_hsa_circ_112774,RMVar_hsa_circ_146039,RMVar_hsa_circ_146040,RMVar_hsa_circ_340038,RMVar_hsa_circ_370695,RMVar_hsa_circ_311081,RMVar_hsa_circ_88319,RMVar_hsa_circ_146041,RMVar_hsa_circ_146043,RMVar_hsa_circ_146044,RMVar_hsa_circ_146042 23438 RMVar_ID_23438 Human_SNP_ID_445004960 A-to-I Human chr10 - 103320818 103320818 103320818 GTGCATGGTTTACAGATATGTGACCTTCATTTATGGTTATTTACTAACAGGAACGAGTAATTCCC GTGCATGGTTTACAGATATGTGACCTTCATTTCTGGTTATTTACTAACAGGAACGAGTAATTCCC T G PCGF6 Ensembl:ENSG00000156374 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7093667 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2248,GWAS_ID_2249,GWAS_ID_2250,GWAS_ID_2251,GWAS_ID_2252,GWAS_ID_2253,GWAS_ID_2254,GWAS_ID_2255,GWAS_ID_2256,GWAS_ID_2257,GWAS_ID_2258,GWAS_ID_2259,GWAS_ID_2260,GWAS_ID_2261,GWAS_ID_2262,GWAS_ID_2263,GWAS_ID_2264,GWAS_ID_2265,GWAS_ID_2266,GWAS_ID_2267,GWAS_ID_2268,GWAS_ID_2269,GWAS_ID_2270,GWAS_ID_2271,GWAS_ID_2272,GWAS_ID_2273,GWAS_ID_2274,GWAS_ID_2275,GWAS_ID_2276,GWAS_ID_2277,GWAS_ID_2278,GWAS_ID_2279,GWAS_ID_2280,GWAS_ID_2281,GWAS_ID_2282 RMVar_hsa_circ_70813,RMVar_hsa_circ_96751,RMVar_hsa_circ_124980,RMVar_hsa_circ_112774,RMVar_hsa_circ_146039,RMVar_hsa_circ_146040,RMVar_hsa_circ_340038,RMVar_hsa_circ_370695,RMVar_hsa_circ_311081,RMVar_hsa_circ_88319,RMVar_hsa_circ_146041,RMVar_hsa_circ_146043,RMVar_hsa_circ_146044,RMVar_hsa_circ_146042 23439 RMVar_ID_23439 Human_SNP_ID_445005828 A-to-I Human chr10 - 103324106 103324105 103324106 GGTGAAACCCTGTCTCTACTAAAAAATGAAAAATAGCTTGGCATGGTGGCACACTCCTGTAATCC GGTGAAACCCTGTCTCTACTAAAAAATGAAAA_TAGCTTGGCATGGTGGCACACTCCTGTAATCC AT A PCGF6 Ensembl:ENSG00000156374 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1171270707 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_70813,RMVar_hsa_circ_96751,RMVar_hsa_circ_124980,RMVar_hsa_circ_112774,RMVar_hsa_circ_146039,RMVar_hsa_circ_146040,RMVar_hsa_circ_340038,RMVar_hsa_circ_370695,RMVar_hsa_circ_311081,RMVar_hsa_circ_88319,RMVar_hsa_circ_146041,RMVar_hsa_circ_146043,RMVar_hsa_circ_146044,RMVar_hsa_circ_146042 23440 RMVar_ID_23440 Human_SNP_ID_445006211 A-to-I Human chr10 - 103325418 103325418 103325418 AAACCCTATCTCTACTAAAAAATACAAAAATTAGCCGGACCTGTTGGCACACACCTGTAATCCCA AAACCCTATCTCTACTAAAAAATACAAAAATTTGCCGGACCTGTTGGCACACACCTGTAATCCCA T A PCGF6 Ensembl:ENSG00000156374 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1380308409 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11248691 RMVar_hsa_circ_70813,RMVar_hsa_circ_96751,RMVar_hsa_circ_124980,RMVar_hsa_circ_112774,RMVar_hsa_circ_146039,RMVar_hsa_circ_146040,RMVar_hsa_circ_340038,RMVar_hsa_circ_370695,RMVar_hsa_circ_311081,RMVar_hsa_circ_88319,RMVar_hsa_circ_146041,RMVar_hsa_circ_146043,RMVar_hsa_circ_146044,RMVar_hsa_circ_146042 23441 RMVar_ID_23441 Human_SNP_ID_445008713 A-to-I Human chr10 - 103335163 103335163 103335163 CATATCTGTACTCCCAGCTGCTCAGGTAGGCTAAGGCAAGAAGTTCACTTAAGCCCAGAAGGTTG CATATCTGTACTCCCAGCTGCTCAGGTAGGCTGAGGCAAGAAGTTCACTTAAGCCCAGAAGGTTG T C PCGF6 Ensembl:ENSG00000156374 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs371771625 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17558857 RMVar_hsa_circ_70813,RMVar_hsa_circ_96751,RMVar_hsa_circ_124980,RMVar_hsa_circ_112774,RMVar_hsa_circ_146039,RMVar_hsa_circ_146040,RMVar_hsa_circ_311081,RMVar_hsa_circ_88319,RMVar_hsa_circ_146043,RMVar_hsa_circ_146044,RMVar_hsa_circ_117490,RMVar_hsa_circ_330925,RMVar_hsa_circ_118653,RMVar_hsa_circ_146045,RMVar_hsa_circ_146046 23442 RMVar_ID_23442 Human_SNP_ID_445008845 A-to-I Human chr10 - 103335589 103335582 103335590 TGGGAGGCCAAGGTGGGCAGATCACGAGATCAAGAGATCGAGGCCATCCTGAACAACATGGTGAA TGGGAGGCCAAGGTGGGCAGATCACGAGATC________GAGGCCATCCTGAACAACATGGTGAA CGATCTCTT C PCGF6 Ensembl:ENSG00000156374 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1262193565 Functional Loss DEL dbSNP153 32..39 33 - - - Human_RBP_ID_11248800 RMVar_hsa_circ_70813,RMVar_hsa_circ_96751,RMVar_hsa_circ_124980,RMVar_hsa_circ_112774,RMVar_hsa_circ_146039,RMVar_hsa_circ_146040,RMVar_hsa_circ_311081,RMVar_hsa_circ_88319,RMVar_hsa_circ_146043,RMVar_hsa_circ_146044,RMVar_hsa_circ_117490,RMVar_hsa_circ_330925,RMVar_hsa_circ_118653,RMVar_hsa_circ_146045,RMVar_hsa_circ_146046 23443 RMVar_ID_23443 Human_SNP_ID_445008904 A-to-I Human chr10 - 103335746 103335744 103335747 GGCCCGGCTGCTCTTGAACTCCTGACCTCATTATCTGCCCACCTTGGCCTCCCAAAGTGCTGGGA GGCCCGGCTGCTCTTGAACTCCTGACCTCAT___CTGCCCACCTTGGCCTCCCAAAGTGCTGGGA GATA G PCGF6 Ensembl:ENSG00000156374 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1208933533 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_70813,RMVar_hsa_circ_96751,RMVar_hsa_circ_124980,RMVar_hsa_circ_112774,RMVar_hsa_circ_146039,RMVar_hsa_circ_146040,RMVar_hsa_circ_311081,RMVar_hsa_circ_88319,RMVar_hsa_circ_146043,RMVar_hsa_circ_146044,RMVar_hsa_circ_117490,RMVar_hsa_circ_330925,RMVar_hsa_circ_118653,RMVar_hsa_circ_146045,RMVar_hsa_circ_146046 23444 RMVar_ID_23444 Human_SNP_ID_445008905 A-to-I Human chr10 - 103335746 103335746 103335746 GGCCCGGCTGCTCTTGAACTCCTGACCTCATTATCTGCCCACCTTGGCCTCCCAAAGTGCTGGGA GGCCCGGCTGCTCTTGAACTCCTGACCTCATTGTCTGCCCACCTTGGCCTCCCAAAGTGCTGGGA T C PCGF6 Ensembl:ENSG00000156374 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1488592443 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70813,RMVar_hsa_circ_96751,RMVar_hsa_circ_124980,RMVar_hsa_circ_112774,RMVar_hsa_circ_146039,RMVar_hsa_circ_146040,RMVar_hsa_circ_311081,RMVar_hsa_circ_88319,RMVar_hsa_circ_146043,RMVar_hsa_circ_146044,RMVar_hsa_circ_117490,RMVar_hsa_circ_330925,RMVar_hsa_circ_118653,RMVar_hsa_circ_146045,RMVar_hsa_circ_146046 23445 RMVar_ID_23445 Human_SNP_ID_445009875 A-to-I Human chr10 - 103339303 103339303 103339303 TTACTGCAGCCTCTGCCTCCTATACTCAAGCAATCCTCTCGCCTCAGCCTCCTGAGCAGCTGGGA TTACTGCAGCCTCTGCCTCCTATACTCAAGCAGTCCTCTCGCCTCAGCCTCCTGAGCAGCTGGGA T C PCGF6 Ensembl:ENSG00000156374 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1457170575 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70813,RMVar_hsa_circ_96751,RMVar_hsa_circ_124980,RMVar_hsa_circ_112774,RMVar_hsa_circ_146039,RMVar_hsa_circ_146040,RMVar_hsa_circ_311081,RMVar_hsa_circ_88319,RMVar_hsa_circ_146043,RMVar_hsa_circ_146044,RMVar_hsa_circ_117490,RMVar_hsa_circ_330925,RMVar_hsa_circ_118653,RMVar_hsa_circ_146045,RMVar_hsa_circ_146046 23446 RMVar_ID_23446 Human_SNP_ID_445010514 A-to-I Human chr10 - 103340799 103340799 103340799 CAGGAGCTGGACACTAGCCTGGTCAACATGGTAAAACCCTGTCTCTACAAAAAAATACGAAAAGA CAGGAGCTGGACACTAGCCTGGTCAACATGGTGAAACCCTGTCTCTACAAAAAAATACGAAAAGA T C PCGF6 Ensembl:ENSG00000156374 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1184876589 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70813,RMVar_hsa_circ_96751,RMVar_hsa_circ_146039,RMVar_hsa_circ_311081,RMVar_hsa_circ_88319,RMVar_hsa_circ_146044,RMVar_hsa_circ_330925 23447 RMVar_ID_23447 Human_SNP_ID_445010857 A-to-I Human chr10 - 103342095 103342095 103342095 ACTGTCTCTATCAAAAGTATAAAAAATTAGCTAGGTGTGGTGGCACGTGCCTGTGATTCCAGCTA ACTGTCTCTATCAAAAGTATAAAAAATTAGCTCGGTGTGGTGGCACGTGCCTGTGATTCCAGCTA T G PCGF6 Ensembl:ENSG00000156374 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1040297092 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70813,RMVar_hsa_circ_96751,RMVar_hsa_circ_146039,RMVar_hsa_circ_311081,RMVar_hsa_circ_88319,RMVar_hsa_circ_146044,RMVar_hsa_circ_330925 23448 RMVar_ID_23448 Human_SNP_ID_445023834 A-to-I Human chr10 - 103389767 103389767 103389767 AGATTGCGCTGCTACACTCCATCCTGGGGGATAGAGCGAGACTGTGTCTCCGAACAAAAAAAAAA AGATTGCGCTGCTACACTCCATCCTGGGGGATGGAGCGAGACTGTGTCTCCGAACAAAAAAAAAA T C ATP5MD Ensembl:ENSG00000173915 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1473511325 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_146065,RMVar_hsa_circ_119476,RMVar_hsa_circ_107147,RMVar_hsa_circ_146064 23449 RMVar_ID_23449 Human_SNP_ID_445023835 A-to-I Human chr10 + 103389768 103389768 103389768 TTTTTTTTTGTTCGGAGACACAGTCTCGCTCTATCCCCCAGGATGGAGTGTAGCAGCGCAATCTC TTTTTTTTTGTTCGGAGACACAGTCTCGCTCTGTCCCCCAGGATGGAGTGTAGCAGCGCAATCTC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs563978319 Functional Loss SNV dbSNP153 33..33 33 - - - 23450 RMVar_ID_23450 Human_SNP_ID_445023857 A-to-I Human chr10 - 103389824 103389824 103389824 GAGAGGCTGAGGCGTGAGAATCACTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCCGAGATTGCG GAGAGGCTGAGGCGTGAGAATCACTTGAACCCGGGAGGCAGAGGTTGCAGTGAGCCGAGATTGCG T C ATP5MD Ensembl:ENSG00000173915 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1378800307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11249105 RMVar_hsa_circ_146065,RMVar_hsa_circ_119476,RMVar_hsa_circ_107147,RMVar_hsa_circ_146064 23451 RMVar_ID_23451 Human_SNP_ID_445024000 A-to-I Human chr10 - 103390442 103390442 103390442 TTGCCCAGGCTGGAGTGAAGTGGTGCGATCTCAGATCACTGCAACCTCTGCTTCCCGGGCTCAAG TTGCCCAGGCTGGAGTGAAGTGGTGCGATCTCGGATCACTGCAACCTCTGCTTCCCGGGCTCAAG T C ATP5MD Ensembl:ENSG00000173915 Protein coding intron GSE38233;GSE100210;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 24183664,29129909,30559470 RNA-Seq:(High) rs1194251259 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11249115,Human_RBP_ID_24777509 RMVar_hsa_circ_146065,RMVar_hsa_circ_119476,RMVar_hsa_circ_107147,RMVar_hsa_circ_146064 23452 RMVar_ID_23452 Human_SNP_ID_445024021 A-to-I Human chr10 - 103390530 103390530 103390530 CCCGCCTTGGCTTCCCAAAGTGTTGGGATTACAGGTGTGAGCCACCACACCCAGCCCGGATATTT CCCGCCTTGGCTTCCCAAAGTGTTGGGATTACTGGTGTGAGCCACCACACCCAGCCCGGATATTT T A ATP5MD Ensembl:ENSG00000173915 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs986954249 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_146065,RMVar_hsa_circ_119476,RMVar_hsa_circ_107147,RMVar_hsa_circ_146064 23453 RMVar_ID_23453 Human_SNP_ID_445024022 A-to-I Human chr10 - 103390530 103390530 103390530 CCCGCCTTGGCTTCCCAAAGTGTTGGGATTACAGGTGTGAGCCACCACACCCAGCCCGGATATTT CCCGCCTTGGCTTCCCAAAGTGTTGGGATTACGGGTGTGAGCCACCACACCCAGCCCGGATATTT T C ATP5MD Ensembl:ENSG00000173915 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs986954249 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_146065,RMVar_hsa_circ_119476,RMVar_hsa_circ_107147,RMVar_hsa_circ_146064 23454 RMVar_ID_23454 Human_SNP_ID_445024069 A-to-I Human chr10 - 103390709 103390709 103390709 CTTGGCTCACTGCAACCTCTGCCTCCCGGTTCAAACAATTCTCCTGCCTCAGGCTCCTGAGTAGC CTTGGCTCACTGCAACCTCTGCCTCCCGGTTCCAACAATTCTCCTGCCTCAGGCTCCTGAGTAGC T G ATP5MD Ensembl:ENSG00000173915 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1180513359 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_146065,RMVar_hsa_circ_119476,RMVar_hsa_circ_107147,RMVar_hsa_circ_146064 23455 RMVar_ID_23455 Human_SNP_ID_445024076 A-to-I Human chr10 - 103390751 103390751 103390751 AGTTTGACTCTTGTTGCCCAGGCTGGAGTGCAATGGCATGATCTTGGCTCACTGCAACCTCTGCC AGTTTGACTCTTGTTGCCCAGGCTGGAGTGCAGTGGCATGATCTTGGCTCACTGCAACCTCTGCC T C ATP5MD Ensembl:ENSG00000173915 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1053771997 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24777518 RMVar_hsa_circ_146065,RMVar_hsa_circ_119476,RMVar_hsa_circ_107147,RMVar_hsa_circ_146064 23456 RMVar_ID_23456 Human_SNP_ID_445024348 A-to-I Human chr10 - 103391780 103391780 103391780 AAAGAGGCTGGGTGCAGTGGCTTGTGCCTGTAATCCCAGCACAATGGGAGGCCGAGGCAGGCGGA AAAGAGGCTGGGTGCAGTGGCTTGTGCCTGTAGTCCCAGCACAATGGGAGGCCGAGGCAGGCGGA T C ATP5MD Ensembl:ENSG00000173915 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs929670757 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_146065,RMVar_hsa_circ_119476,RMVar_hsa_circ_107147,RMVar_hsa_circ_146064 23457 RMVar_ID_23457 Human_SNP_ID_445028590 A-to-I Human chr10 + 103407908 103407908 103407908 ACCCGGCTGGTTTTTGTGTTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTTGTGTCAA ACCCGGCTGGTTTTTGTGTTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTTGTGTCAA A G PDCD11 Ensembl:ENSG00000148843 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1201049355 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10758,RMVar_hsa_circ_118010,RMVar_hsa_circ_81489,RMVar_hsa_circ_146068,RMVar_hsa_circ_63666,RMVar_hsa_circ_94196,RMVar_hsa_circ_12218,RMVar_hsa_circ_146070,RMVar_hsa_circ_323756,RMVar_hsa_circ_123193,RMVar_hsa_circ_146071,RMVar_hsa_circ_304056,RMVar_hsa_circ_99127,RMVar_hsa_circ_146073,RMVar_hsa_circ_90131,RMVar_hsa_circ_121000,RMVar_hsa_circ_146074,RMVar_hsa_circ_122085,RMVar_hsa_circ_90390,RMVar_hsa_circ_31612,RMVar_hsa_circ_85577,RMVar_hsa_circ_18662,RMVar_hsa_circ_108139,RMVar_hsa_circ_146077,RMVar_hsa_circ_146079,RMVar_hsa_circ_146080,RMVar_hsa_circ_146081,RMVar_hsa_circ_146078,RMVar_hsa_circ_146076,RMVar_hsa_circ_118342,RMVar_hsa_circ_146082,RMVar_hsa_circ_146083 23458 RMVar_ID_23458 Human_SNP_ID_445029118 A-to-I Human chr10 + 103410141 103410141 103410141 CCTGTAGTCCCAGCTACTCAGGAAGGTGAGGCAGGAGAATCGCTTGAACCCGGGAGGCCGAGGTT CCTGTAGTCCCAGCTACTCAGGAAGGTGAGGCGGGAGAATCGCTTGAACCCGGGAGGCCGAGGTT A G PDCD11 Ensembl:ENSG00000148843 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs926609546 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10758,RMVar_hsa_circ_118010,RMVar_hsa_circ_81489,RMVar_hsa_circ_146068,RMVar_hsa_circ_63666,RMVar_hsa_circ_94196,RMVar_hsa_circ_146070,RMVar_hsa_circ_123193,RMVar_hsa_circ_146071,RMVar_hsa_circ_99127,RMVar_hsa_circ_146073,RMVar_hsa_circ_90131,RMVar_hsa_circ_121000,RMVar_hsa_circ_146074,RMVar_hsa_circ_122085,RMVar_hsa_circ_90390,RMVar_hsa_circ_31612,RMVar_hsa_circ_85577,RMVar_hsa_circ_76946,RMVar_hsa_circ_108139,RMVar_hsa_circ_146077,RMVar_hsa_circ_146079,RMVar_hsa_circ_146080,RMVar_hsa_circ_146081,RMVar_hsa_circ_146078,RMVar_hsa_circ_118342,RMVar_hsa_circ_113747,RMVar_hsa_circ_146082,RMVar_hsa_circ_146083,RMVar_hsa_circ_119264,RMVar_hsa_circ_84752,RMVar_hsa_circ_146085,RMVar_hsa_circ_146086,RMVar_hsa_circ_146087,RMVar_hsa_circ_146084 23459 RMVar_ID_23459 Human_SNP_ID_445029134 A-to-I Human chr10 + 103410210 103410210 103410210 TGAGCTGAGATCGTGCCACTGCACTCCAGCCTAGACAACAGAGCGAGACTCCATCTCAAAAAAAA TGAGCTGAGATCGTGCCACTGCACTCCAGCCTGGACAACAGAGCGAGACTCCATCTCAAAAAAAA A G PDCD11 Ensembl:ENSG00000148843 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1008292197 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10758,RMVar_hsa_circ_118010,RMVar_hsa_circ_81489,RMVar_hsa_circ_146068,RMVar_hsa_circ_63666,RMVar_hsa_circ_94196,RMVar_hsa_circ_146070,RMVar_hsa_circ_123193,RMVar_hsa_circ_146071,RMVar_hsa_circ_99127,RMVar_hsa_circ_146073,RMVar_hsa_circ_90131,RMVar_hsa_circ_121000,RMVar_hsa_circ_146074,RMVar_hsa_circ_122085,RMVar_hsa_circ_90390,RMVar_hsa_circ_31612,RMVar_hsa_circ_85577,RMVar_hsa_circ_76946,RMVar_hsa_circ_108139,RMVar_hsa_circ_146077,RMVar_hsa_circ_146079,RMVar_hsa_circ_146080,RMVar_hsa_circ_146081,RMVar_hsa_circ_146078,RMVar_hsa_circ_118342,RMVar_hsa_circ_113747,RMVar_hsa_circ_146082,RMVar_hsa_circ_146083,RMVar_hsa_circ_119264,RMVar_hsa_circ_84752,RMVar_hsa_circ_146085,RMVar_hsa_circ_146086,RMVar_hsa_circ_146087,RMVar_hsa_circ_146084 23460 RMVar_ID_23460 Human_SNP_ID_445029571 A-to-I Human chr10 + 103411679 103411679 103411679 CTAAAGTGCTGGGATTATAGGCTTCAGCCACTACAACTAGCTGAGAATTTTTTTTTAAAGTGAAA CTAAAGTGCTGGGATTATAGGCTTCAGCCACTGCAACTAGCTGAGAATTTTTTTTTAAAGTGAAA A G PDCD11 Ensembl:ENSG00000148843 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs868748462 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10758,RMVar_hsa_circ_118010,RMVar_hsa_circ_81489,RMVar_hsa_circ_146068,RMVar_hsa_circ_63666,RMVar_hsa_circ_94196,RMVar_hsa_circ_146070,RMVar_hsa_circ_123193,RMVar_hsa_circ_146071,RMVar_hsa_circ_99127,RMVar_hsa_circ_146073,RMVar_hsa_circ_90131,RMVar_hsa_circ_121000,RMVar_hsa_circ_146074,RMVar_hsa_circ_122085,RMVar_hsa_circ_90390,RMVar_hsa_circ_31612,RMVar_hsa_circ_85577,RMVar_hsa_circ_76946,RMVar_hsa_circ_108139,RMVar_hsa_circ_146077,RMVar_hsa_circ_146079,RMVar_hsa_circ_146080,RMVar_hsa_circ_146081,RMVar_hsa_circ_146078,RMVar_hsa_circ_118342,RMVar_hsa_circ_113747,RMVar_hsa_circ_146082,RMVar_hsa_circ_146083,RMVar_hsa_circ_119264,RMVar_hsa_circ_84752,RMVar_hsa_circ_146085,RMVar_hsa_circ_146086,RMVar_hsa_circ_146087,RMVar_hsa_circ_146084 23461 RMVar_ID_23461 Human_SNP_ID_445032503 A-to-I Human chr10 + 103422270 103422269 103422271 GTCTGGCTAATTTTTGTATTTTTAGAGAAGACAGGGTTTCGCCATGTTGGCCAGGCTGGTCTCGA GTCTGGCTAATTTTTGTATTTTTAGAGAAGAC__GGTTTCGCCATGTTGGCCAGGCTGGTCTCGA CAG C PDCD11 Ensembl:ENSG00000148843 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1365068204 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_10758,RMVar_hsa_circ_118010,RMVar_hsa_circ_81489,RMVar_hsa_circ_146068,RMVar_hsa_circ_63666,RMVar_hsa_circ_94196,RMVar_hsa_circ_146070,RMVar_hsa_circ_146071,RMVar_hsa_circ_99127,RMVar_hsa_circ_90131,RMVar_hsa_circ_146074,RMVar_hsa_circ_122085,RMVar_hsa_circ_85577,RMVar_hsa_circ_83506,RMVar_hsa_circ_76946,RMVar_hsa_circ_108139,RMVar_hsa_circ_146079,RMVar_hsa_circ_146080,RMVar_hsa_circ_146081,RMVar_hsa_circ_118342,RMVar_hsa_circ_146082,RMVar_hsa_circ_146083,RMVar_hsa_circ_119264,RMVar_hsa_circ_109504,RMVar_hsa_circ_146085,RMVar_hsa_circ_146084,RMVar_hsa_circ_111901,RMVar_hsa_circ_91545,RMVar_hsa_circ_107178,RMVar_hsa_circ_90955,RMVar_hsa_circ_96829,RMVar_hsa_circ_146090,RMVar_hsa_circ_146092,RMVar_hsa_circ_146093,RMVar_hsa_circ_146094,RMVar_hsa_circ_146091,RMVar_hsa_circ_146089,RMVar_hsa_circ_101788,RMVar_hsa_circ_146095,RMVar_hsa_circ_91434,RMVar_hsa_circ_92169,RMVar_hsa_circ_122458,RMVar_hsa_circ_146096,RMVar_hsa_circ_146097,RMVar_hsa_circ_146098,RMVar_hsa_circ_107334,RMVar_hsa_circ_146099,RMVar_hsa_circ_146100,RMVar_hsa_circ_351082,RMVar_hsa_circ_353913,RMVar_hsa_circ_103263,RMVar_hsa_circ_95621,RMVar_hsa_circ_49517,RMVar_hsa_circ_146101,RMVar_hsa_circ_146102,RMVar_hsa_circ_146103,RMVar_hsa_circ_107933,RMVar_hsa_circ_146104,RMVar_hsa_circ_26562,RMVar_hsa_circ_93294,RMVar_hsa_circ_146105,RMVar_hsa_circ_146106 23462 RMVar_ID_23462 Human_SNP_ID_445032504 A-to-I Human chr10 + 103422270 103422270 103422270 GTCTGGCTAATTTTTGTATTTTTAGAGAAGACAGGGTTTCGCCATGTTGGCCAGGCTGGTCTCGA GTCTGGCTAATTTTTGTATTTTTAGAGAAGACCGGGTTTCGCCATGTTGGCCAGGCTGGTCTCGA A C PDCD11 Ensembl:ENSG00000148843 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs755430171 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10758,RMVar_hsa_circ_118010,RMVar_hsa_circ_81489,RMVar_hsa_circ_146068,RMVar_hsa_circ_63666,RMVar_hsa_circ_94196,RMVar_hsa_circ_146070,RMVar_hsa_circ_146071,RMVar_hsa_circ_99127,RMVar_hsa_circ_90131,RMVar_hsa_circ_146074,RMVar_hsa_circ_122085,RMVar_hsa_circ_85577,RMVar_hsa_circ_83506,RMVar_hsa_circ_76946,RMVar_hsa_circ_108139,RMVar_hsa_circ_146079,RMVar_hsa_circ_146080,RMVar_hsa_circ_146081,RMVar_hsa_circ_118342,RMVar_hsa_circ_146082,RMVar_hsa_circ_146083,RMVar_hsa_circ_119264,RMVar_hsa_circ_109504,RMVar_hsa_circ_146085,RMVar_hsa_circ_146084,RMVar_hsa_circ_111901,RMVar_hsa_circ_91545,RMVar_hsa_circ_107178,RMVar_hsa_circ_90955,RMVar_hsa_circ_96829,RMVar_hsa_circ_146090,RMVar_hsa_circ_146092,RMVar_hsa_circ_146093,RMVar_hsa_circ_146094,RMVar_hsa_circ_146091,RMVar_hsa_circ_146089,RMVar_hsa_circ_101788,RMVar_hsa_circ_146095,RMVar_hsa_circ_91434,RMVar_hsa_circ_92169,RMVar_hsa_circ_122458,RMVar_hsa_circ_146096,RMVar_hsa_circ_146097,RMVar_hsa_circ_146098,RMVar_hsa_circ_107334,RMVar_hsa_circ_146099,RMVar_hsa_circ_146100,RMVar_hsa_circ_351082,RMVar_hsa_circ_353913,RMVar_hsa_circ_103263,RMVar_hsa_circ_95621,RMVar_hsa_circ_49517,RMVar_hsa_circ_146101,RMVar_hsa_circ_146102,RMVar_hsa_circ_146103,RMVar_hsa_circ_107933,RMVar_hsa_circ_146104,RMVar_hsa_circ_26562,RMVar_hsa_circ_93294,RMVar_hsa_circ_146105,RMVar_hsa_circ_146106 23463 RMVar_ID_23463 Human_SNP_ID_445033465 A-to-I Human chr10 + 103425819 103425819 103425819 CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCACCCACCACCACGCCCGGCTAACTTTT CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTGCAGGCACCCACCACCACGCCCGGCTAACTTTT A G PDCD11 Ensembl:ENSG00000148843 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1463588466 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10758,RMVar_hsa_circ_118010,RMVar_hsa_circ_81489,RMVar_hsa_circ_146068,RMVar_hsa_circ_94196,RMVar_hsa_circ_146070,RMVar_hsa_circ_146071,RMVar_hsa_circ_99127,RMVar_hsa_circ_146074,RMVar_hsa_circ_122085,RMVar_hsa_circ_85577,RMVar_hsa_circ_76946,RMVar_hsa_circ_146080,RMVar_hsa_circ_146081,RMVar_hsa_circ_118342,RMVar_hsa_circ_146083,RMVar_hsa_circ_109504,RMVar_hsa_circ_146084,RMVar_hsa_circ_111901,RMVar_hsa_circ_91545,RMVar_hsa_circ_107178,RMVar_hsa_circ_90955,RMVar_hsa_circ_96829,RMVar_hsa_circ_146090,RMVar_hsa_circ_146092,RMVar_hsa_circ_146093,RMVar_hsa_circ_146094,RMVar_hsa_circ_146091,RMVar_hsa_circ_101788,RMVar_hsa_circ_146095,RMVar_hsa_circ_91434,RMVar_hsa_circ_92169,RMVar_hsa_circ_122458,RMVar_hsa_circ_146096,RMVar_hsa_circ_146097,RMVar_hsa_circ_146098,RMVar_hsa_circ_107334,RMVar_hsa_circ_146099,RMVar_hsa_circ_146100,RMVar_hsa_circ_351082,RMVar_hsa_circ_353913,RMVar_hsa_circ_103263,RMVar_hsa_circ_95621,RMVar_hsa_circ_146101,RMVar_hsa_circ_146102,RMVar_hsa_circ_146103,RMVar_hsa_circ_107933,RMVar_hsa_circ_146104,RMVar_hsa_circ_26562,RMVar_hsa_circ_93294,RMVar_hsa_circ_112152,RMVar_hsa_circ_146105,RMVar_hsa_circ_146106,RMVar_hsa_circ_360813,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_146110 23464 RMVar_ID_23464 Human_SNP_ID_445033606 A-to-I Human chr10 + 103426634 103426634 103426634 CTGGCCAACATGGTGAAACCCCGTCTACTGAAAAAACAAAAATTAGCCGGGCACAGTGCCTGTAG CTGGCCAACATGGTGAAACCCCGTCTACTGAAGAAACAAAAATTAGCCGGGCACAGTGCCTGTAG A G PDCD11 Ensembl:ENSG00000148843 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1043481257 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10758,RMVar_hsa_circ_118010,RMVar_hsa_circ_81489,RMVar_hsa_circ_146068,RMVar_hsa_circ_94196,RMVar_hsa_circ_146070,RMVar_hsa_circ_146071,RMVar_hsa_circ_99127,RMVar_hsa_circ_146074,RMVar_hsa_circ_122085,RMVar_hsa_circ_85577,RMVar_hsa_circ_76946,RMVar_hsa_circ_146080,RMVar_hsa_circ_146081,RMVar_hsa_circ_118342,RMVar_hsa_circ_146083,RMVar_hsa_circ_109504,RMVar_hsa_circ_146084,RMVar_hsa_circ_111901,RMVar_hsa_circ_91545,RMVar_hsa_circ_107178,RMVar_hsa_circ_90955,RMVar_hsa_circ_96829,RMVar_hsa_circ_146090,RMVar_hsa_circ_146092,RMVar_hsa_circ_146093,RMVar_hsa_circ_146094,RMVar_hsa_circ_146091,RMVar_hsa_circ_101788,RMVar_hsa_circ_146095,RMVar_hsa_circ_91434,RMVar_hsa_circ_92169,RMVar_hsa_circ_122458,RMVar_hsa_circ_146096,RMVar_hsa_circ_146097,RMVar_hsa_circ_146098,RMVar_hsa_circ_107334,RMVar_hsa_circ_146099,RMVar_hsa_circ_146100,RMVar_hsa_circ_351082,RMVar_hsa_circ_353913,RMVar_hsa_circ_103263,RMVar_hsa_circ_95621,RMVar_hsa_circ_146101,RMVar_hsa_circ_146102,RMVar_hsa_circ_146103,RMVar_hsa_circ_107933,RMVar_hsa_circ_146104,RMVar_hsa_circ_26562,RMVar_hsa_circ_93294,RMVar_hsa_circ_112152,RMVar_hsa_circ_146105,RMVar_hsa_circ_146106,RMVar_hsa_circ_360813,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_146110 23465 RMVar_ID_23465 Human_SNP_ID_445033706 A-to-I Human chr10 + 103426986 103426986 103426986 TAAAAATTAGCTGGGCATGGTGGCATACACCTATAGTCCCAGCTACTTGGGAGGCTGAGCTGGGA TAAAAATTAGCTGGGCATGGTGGCATACACCTGTAGTCCCAGCTACTTGGGAGGCTGAGCTGGGA A G PDCD11 Ensembl:ENSG00000148843 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1463671680 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24777656 RMVar_hsa_circ_10758,RMVar_hsa_circ_118010,RMVar_hsa_circ_81489,RMVar_hsa_circ_146068,RMVar_hsa_circ_94196,RMVar_hsa_circ_146070,RMVar_hsa_circ_146071,RMVar_hsa_circ_99127,RMVar_hsa_circ_146074,RMVar_hsa_circ_122085,RMVar_hsa_circ_85577,RMVar_hsa_circ_76946,RMVar_hsa_circ_146080,RMVar_hsa_circ_146081,RMVar_hsa_circ_118342,RMVar_hsa_circ_146083,RMVar_hsa_circ_109504,RMVar_hsa_circ_146084,RMVar_hsa_circ_111901,RMVar_hsa_circ_91545,RMVar_hsa_circ_107178,RMVar_hsa_circ_90955,RMVar_hsa_circ_96829,RMVar_hsa_circ_146090,RMVar_hsa_circ_146092,RMVar_hsa_circ_146093,RMVar_hsa_circ_146094,RMVar_hsa_circ_146091,RMVar_hsa_circ_101788,RMVar_hsa_circ_146095,RMVar_hsa_circ_91434,RMVar_hsa_circ_92169,RMVar_hsa_circ_122458,RMVar_hsa_circ_146096,RMVar_hsa_circ_146097,RMVar_hsa_circ_146098,RMVar_hsa_circ_107334,RMVar_hsa_circ_146099,RMVar_hsa_circ_146100,RMVar_hsa_circ_351082,RMVar_hsa_circ_353913,RMVar_hsa_circ_103263,RMVar_hsa_circ_95621,RMVar_hsa_circ_146101,RMVar_hsa_circ_146102,RMVar_hsa_circ_146103,RMVar_hsa_circ_107933,RMVar_hsa_circ_146104,RMVar_hsa_circ_26562,RMVar_hsa_circ_93294,RMVar_hsa_circ_112152,RMVar_hsa_circ_146105,RMVar_hsa_circ_146106,RMVar_hsa_circ_360813,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_146110 23466 RMVar_ID_23466 Human_SNP_ID_445038542 A-to-I Human chr10 - 103445934 103445934 103445934 GGCCCACTCCCTGGAGCCTACTGACCCCCTCCAGCTGGACTGACAGCCTGCCAGGGACAAAGCAG GGCCCACTCCCTGGAGCCTACTGACCCCCTCCGGCTGGACTGACAGCCTGCCAGGGACAAAGCAG T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs550082661 Functional Loss SNV dbSNP153 33..33 33 - - - 23467 RMVar_ID_23467 Human_SNP_ID_445039191 A-to-I Human chr10 - 103448284 103448284 103448284 AAATTAGCCAGGAGTGGTGGTGGGCACCTGTAATCTCAGCTACTTGGGAGGCTGAGGCAGGAGAA AAATTAGCCAGGAGTGGTGGTGGGCACCTGTAGTCTCAGCTACTTGGGAGGCTGAGGCAGGAGAA T C CALHM2 Ensembl:ENSG00000138172 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1383824804 Functional Loss SNV dbSNP153 33..33 33 - - - 23468 RMVar_ID_23468 Human_SNP_ID_445039266 A-to-I Human chr10 + 103448568 103448568 103448568 ATGGCGAAACCCCATCTCTACTAAAAATACAAAAATTAGGTGGATGTGGTGGCTGCGTGCCTGTA ATGGCGAAACCCCATCTCTACTAAAAATACAATAATTAGGTGGATGTGGTGGCTGCGTGCCTGTA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs944680502 Functional Loss SNV dbSNP153 33..33 33 - - - 23469 RMVar_ID_23469 Human_SNP_ID_445039268 A-to-I Human chr10 - 103448572 103448572 103448572 GGATTACAGGCACGCAGCCACCACATCCACCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCG GGATTACAGGCACGCAGCCACCACATCCACCTGATTTTTGTATTTTTAGTAGAGATGGGGTTTCG T C CALHM2 Ensembl:ENSG00000138172 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1350312169 Functional Loss SNV dbSNP153 33..33 33 - - - 23470 RMVar_ID_23470 Human_SNP_ID_445079165 A-to-I Human chr10 + 103609065 103609064 103609065 GTGGTCCCAGCTACTTGGGAGTCTGAGGCAGGAAAATAGCGTGAGCCCAGGAGTTCGAGGCTGCA GTGGTCCCAGCTACTTGGGAGTCTGAGGCAGG_AAATAGCGTGAGCCCAGGAGTTCGAGGCTGCA GA G AL121929.3 Ensembl:ENSG00000273108 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1360555367 Functional Loss DEL dbSNP153 33..33 33 - - - 23471 RMVar_ID_23471 Human_SNP_ID_445090032 A-to-I Human chr10 - 103655580 103655580 103655580 TCAGTAGAGATGGGGTTTTACCAAGTTGGTCAAGCTGGTCTTGAACTCCTGGCCTCAAATGATCC TCAGTAGAGATGGGGTTTTACCAAGTTGGTCACGCTGGTCTTGAACTCCTGGCCTCAAATGATCC T G SH3PXD2A Ensembl:ENSG00000107957 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404340498 Functional Loss SNV dbSNP153 33..33 33 - - - 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 23472 RMVar_ID_23472 Human_SNP_ID_445096965 A-to-I Human chr10 - 103684811 103684811 103684811 TTGCCCAGGGTGGTCTTGAACTCCTAGGATCAAGTGACTATCCTGCCTCGGCCTCCCAAAGTGCT TTGCCCAGGGTGGTCTTGAACTCCTAGGATCAGGTGACTATCCTGCCTCGGCCTCCCAAAGTGCT T C SH3PXD2A Ensembl:ENSG00000107957 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,frontal_cortex - 29129909,30559470 RNA-Seq:(High) rs993914795 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_324517,RMVar_hsa_circ_71694,RMVar_hsa_circ_19664,RMVar_hsa_circ_108199,RMVar_hsa_circ_41233,RMVar_hsa_circ_146136 23473 RMVar_ID_23473 Human_SNP_ID_445096989 A-to-I Human chr10 - 103684933 103684933 103684933 TCACTGCAGACTTGACCTCCTGGCTTCAAGCAATCCTCTCACCTCAGCCTTCTGAGTAGTTGGGA TCACTGCAGACTTGACCTCCTGGCTTCAAGCAGTCCTCTCACCTCAGCCTTCTGAGTAGTTGGGA T C SH3PXD2A Ensembl:ENSG00000107957 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1200012151 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_324517,RMVar_hsa_circ_71694,RMVar_hsa_circ_19664,RMVar_hsa_circ_108199,RMVar_hsa_circ_41233,RMVar_hsa_circ_146136 23474 RMVar_ID_23474 Human_SNP_ID_445156705 A-to-I Human chr10 - 103936904 103936904 103936904 ACAATGTACCCACCTCGGCCTCCCAAAGTGCTAGAATTACTAACACTTTTGTAAAGTAAAAAGTT ACAATGTACCCACCTCGGCCTCCCAAAGTGCTGGAATTACTAACACTTTTGTAAAGTAAAAAGTT T C lnc-STN1-2,lnc-STN1-2:2 RNACentral:URS0000D5AC0C,RNACentral:URS0000D5CB69 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1356955690 Functional Loss SNV dbSNP153 33..33 33 - - - 23475 RMVar_ID_23475 Human_SNP_ID_445156850 A-to-I Human chr10 - 103937467 103937467 103937467 AGGCGGAGGCTGCAGCGAGCCAAGATCGCACCACTGCACTCTAGCCTGGGCAACAGAGCTAGACT AGGCGGAGGCTGCAGCGAGCCAAGATCGCACCGCTGCACTCTAGCCTGGGCAACAGAGCTAGACT T C lnc-STN1-2,lnc-STN1-2:2 RNACentral:URS0000D5AC0C,RNACentral:URS0000D5CB69 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1372183023 Functional Loss SNV dbSNP153 33..33 33 - - - 23476 RMVar_ID_23476 Human_SNP_ID_445166217 A-to-I Human chr10 + 103975943 103975942 103975944 TTTGTTTTATTATTATTATTTTTTCTTGAGACAGAGTCTCACCTCTGTCATCCAGGCCGGAGTGC TTTGTTTTATTATTATTATTTTTTCTTGAGAC__AGTCTCACCTCTGTCATCCAGGCCGGAGTGC CAG C SLK Ensembl:ENSG00000065613 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1218286086 Functional Loss DEL dbSNP153 33..34 33 - - - 23477 RMVar_ID_23477 Human_SNP_ID_445176214 A-to-I Human chr10 + 104017680 104017680 104017680 TTTTGTATATTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCT TTTTGTATATTTAGTAGAGATGGGGTTTCACCTTGTTGGCCAGGCTGGTCTCGAACTCCTGACCT A T SLK Ensembl:ENSG00000065613 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs989572502 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_354905,RMVar_hsa_circ_146146,RMVar_hsa_circ_52374,RMVar_hsa_circ_63850,RMVar_hsa_circ_353762,RMVar_hsa_circ_295096,RMVar_hsa_circ_355494,RMVar_hsa_circ_308691,RMVar_hsa_circ_146147,RMVar_hsa_circ_146148 23478 RMVar_ID_23478 Human_SNP_ID_445238867 A-to-I Human chr10 + 104280059 104280059 104280059 ATAACGATGTATACCTGTAGTCCCAGCTACTTAGGAGGCTGAGGCAGGAGGATTGCTTGAGTCTG ATAACGATGTATACCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGGATTGCTTGAGTCTG A G GSTO2 Ensembl:ENSG00000065621 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs577425735 Functional Loss SNV dbSNP153 33..33 33 - - - 23479 RMVar_ID_23479 Human_SNP_ID_445239445 A-to-I Human chr10 + 104282479 104282479 104282479 GGGAGGCTGAGATGAGAGGATCACTGGAGCCTAGGAGGTTGAAGCTGCAGTGAGCTATAATTGCA GGGAGGCTGAGATGAGAGGATCACTGGAGCCTTGGAGGTTGAAGCTGCAGTGAGCTATAATTGCA A T GSTO2 Ensembl:ENSG00000065621 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1393178641 Functional Loss SNV dbSNP153 33..33 33 - - - 23480 RMVar_ID_23480 Human_SNP_ID_445240881 A-to-I Human chr10 + 104289296 104289296 104289296 TTGTGTATTTTTTGTAGAGATGGGATTTTGCCATGTTGCCCAGACTGGTCTCGAACTTCTGGGCT TTGTGTATTTTTTGTAGAGATGGGATTTTGCCGTGTTGCCCAGACTGGTCTCGAACTTCTGGGCT A G GSTO2 Ensembl:ENSG00000065621 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1433777282 Functional Loss SNV dbSNP153 33..33 33 - - - 23481 RMVar_ID_23481 Human_SNP_ID_445241134 A-to-I Human chr10 + 104290462 104290462 104290462 GGGAGGCAGAGGTTGCAGTGAGCTGAGATCACACCACTGCACTCCAACTTGGGTGACAGAGTCAC GGGAGGCAGAGGTTGCAGTGAGCTGAGATCACTCCACTGCACTCCAACTTGGGTGACAGAGTCAC A T GSTO2 Ensembl:ENSG00000065621 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1191519575 Functional Loss SNV dbSNP153 33..33 33 - - - 23482 RMVar_ID_23482 Human_SNP_ID_445242652 A-to-I Human chr10 + 104297022 104297022 104297022 GCTGGTCTCGAACTCCCCACCTCAGGTAATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGAATAC GCTGGTCTCGAACTCCCCACCTCAGGTAATCCCCCCGCCTCGGCCTCCCAAAGTGCTGGGAATAC A C GSTO2 Ensembl:ENSG00000065621 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1296774472 Functional Loss SNV dbSNP153 33..33 33 - - - 23483 RMVar_ID_23483 Human_SNP_ID_445250888 A-to-I Human chr10 - 104331089 104331089 104331089 TGCAGAGAAGGCTTTCCATTCCTTTTATCTCAAATAGCCCAGGCCACACTCACAGAATCTTGGTA TGCAGAGAAGGCTTTCCATTCCTTTTATCTCAGATAGCCCAGGCCACACTCACAGAATCTTGGTA T C ITPRIP Ensembl:ENSG00000148841 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1165697010 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104371,RMVar_hsa_circ_146258 23484 RMVar_ID_23484 Human_SNP_ID_654949081 A-to-I Human chr19 - 200742 200739 200743 CTCTCCCGGCCCTGCCTCCCAGCAAGTAAGCAAGCTCTTTTGGCTCAACTCCTGCCCAGCTCCCA CTCTCCCGGCCCTGCCTCCCAGCAAGTAAGC____TCTTTTGGCTCAACTCCTGCCCAGCTCCCA AGCTT A LINC01002,AC010507.2 Ensembl:ENSG00000282508,Ensembl:ENSG00000282339 lincRNA,Pseudogene exon,exon GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1373468752 Functional Loss DEL dbSNP153 32..35 33 - - - 23485 RMVar_ID_23485 Human_SNP_ID_654949082 A-to-I Human chr19 - 200742 200742 200742 CTCTCCCGGCCCTGCCTCCCAGCAAGTAAGCAAGCTCTTTTGGCTCAACTCCTGCCCAGCTCCCA CTCTCCCGGCCCTGCCTCCCAGCAAGTAAGCAGGCTCTTTTGGCTCAACTCCTGCCCAGCTCCCA T C LINC01002,AC010507.2 Ensembl:ENSG00000282508,Ensembl:ENSG00000282339 lincRNA,Pseudogene exon,exon GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1411550328 Functional Loss SNV dbSNP153 33..33 33 - - - 23486 RMVar_ID_23486 Human_SNP_ID_654967906 A-to-I Human chr19 - 289526 289526 289526 TATTTTTAGTAGAGTTGGGGTTTCACCGTGTTAGCCAGGATGGTCTCGATCTCCTGACCTCGTGA TATTTTTAGTAGAGTTGGGGTTTCACCGTGTTGGCCAGGATGGTCTCGATCTCCTGACCTCGTGA T C PLPP2 Ensembl:ENSG00000141934 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs759457161 Functional Loss SNV dbSNP153 33..33 33 - - - 23487 RMVar_ID_23487 Human_SNP_ID_655052037 A-to-I Human chr19 + 520366 520365 520367 ACGAAAAAAAAAAAAAGCTGGGCTGTGGTGGCAGGCGCCTGTAATCCCAGCTACTCAGGAGGCTG ACGAAAAAAAAAAAAAGCTGGGCTGTGGTGGC__GCGCCTGTAATCCCAGCTACTCAGGAGGCTG CAG C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1196246295 Functional Loss DEL dbSNP153 33..34 33 - - - 23488 RMVar_ID_23488 Human_SNP_ID_655052038 A-to-I Human chr19 + 520366 520366 520366 ACGAAAAAAAAAAAAAGCTGGGCTGTGGTGGCAGGCGCCTGTAATCCCAGCTACTCAGGAGGCTG ACGAAAAAAAAAAAAAGCTGGGCTGTGGTGGCGGGCGCCTGTAATCCCAGCTACTCAGGAGGCTG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs568284063 Functional Loss SNV dbSNP153 33..33 33 - - - 23489 RMVar_ID_23489 Human_SNP_ID_655069138 A-to-I Human chr19 - 562104 562104 562104 CCTGTCATCCTAGCACTTCGGGAGGCCGAGGCAGGAGGATCACGAGGTCAGGAGATCGAGACAAT CCTGTCATCCTAGCACTTCGGGAGGCCGAGGCGGGAGGATCACGAGGTCAGGAGATCGAGACAAT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs901527077 Functional Loss SNV dbSNP153 33..33 33 - - - 23490 RMVar_ID_23490 Human_SNP_ID_655069419 A-to-I Human chr19 - 562883 562883 562883 CTGGGAGGTGGAGGTTGCAGTGAGCCGAGATCACGCCCACCGCACTCCAGCCTGGGCGACAGAGC CTGGGAGGTGGAGGTTGCAGTGAGCCGAGATCGCGCCCACCGCACTCCAGCCTGGGCGACAGAGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1187679891 Functional Loss SNV dbSNP153 33..33 33 - - - 23491 RMVar_ID_23491 Human_SNP_ID_655069688 A-to-I Human chr19 - 563584 563584 563584 GTCCCACTGCACTCCAGCCTGGGTGACAGAACAAGACTCCATCTCAAAAAAAAGAGGCAACCTCC GTCCCACTGCACTCCAGCCTGGGTGACAGAACGAGACTCCATCTCAAAAAAAAGAGGCAACCTCC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459769740 Functional Loss SNV dbSNP153 33..33 33 - - - 23492 RMVar_ID_23492 Human_SNP_ID_655089652 A-to-I Human chr19 + 612490 612490 612490 CGGGCTCCAGTGCAGTTGTGTGATCTTGGTTCACTGTAACCTCCTCCTCCCGGGTTCAAGAGACT CGGGCTCCAGTGCAGTTGTGTGATCTTGGTTCGCTGTAACCTCCTCCTCCCGGGTTCAAGAGACT A G HCN2 Ensembl:ENSG00000099822 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256691639 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_53125 23493 RMVar_ID_23493 Human_SNP_ID_655098459 A-to-I Human chr19 - 625876 625876 625876 CAGCATGGTGAAACCCCGTATCTGCTAAGAATACAAAAAATTAGCTGGTGTGGTGGCGTGTGCCT CAGCATGGTGAAACCCCGTATCTGCTAAGAATGCAAAAAATTAGCTGGTGTGGTGGCGTGTGCCT T C POLRMT Ensembl:ENSG00000099821 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1341314743 Functional Loss SNV dbSNP153 33..33 33 - - - 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 23494 RMVar_ID_23494 Human_SNP_ID_655099276 A-to-I Human chr19 - 627759 627759 627759 CACCACGCCCGGCCAATTTTTGTATTTTTAGTAGAGACGGGCTTTTGCCATGTTGGCCGGGCTGG CACCACGCCCGGCCAATTTTTGTATTTTTAGTGGAGACGGGCTTTTGCCATGTTGGCCGGGCTGG T C POLRMT Ensembl:ENSG00000099821 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053978156 Functional Loss SNV dbSNP153 33..33 33 - - - 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 23495 RMVar_ID_23495 Human_SNP_ID_655115056 A-to-I Human chr19 + 666674 666674 666674 GACCTCAGGTGATCCGCCCACCTCAGCCTCCCAAAGTGCTGGGATCACAGGCGTGAGGCTAATCG GACCTCAGGTGATCCGCCCACCTCAGCCTCCCGAAGTGCTGGGATCACAGGCGTGAGGCTAATCG A G AC004156.1 Ensembl:ENSG00000267666 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1281901074 Functional Loss SNV dbSNP153 33..33 33 - - - 23496 RMVar_ID_23496 Human_SNP_ID_655156815 A-to-I Human chr19 + 785002 785002 785002 AGTGATGTTTCCAGGCCGGGCGCGCTTGTAATACCAGCATTTGGGAGGCTGAGGCAGGCGGATCA AGTGATGTTTCCAGGCCGGGCGCGCTTGTAATCCCAGCATTTGGGAGGCTGAGGCAGGCGGATCA A C LINC01836 Ensembl:ENSG00000267530 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs374456148 Functional Loss SNV dbSNP153 33..33 33 - - - 23497 RMVar_ID_23497 Human_SNP_ID_655157066 A-to-I Human chr19 + 785514 785514 785514 CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACACGCGTGTGCCACCACGCCAGGCTAATTTTT CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTGCACGCGTGTGCCACCACGCCAGGCTAATTTTT A G LINC01836 Ensembl:ENSG00000267530 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs972219757 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1928940 23498 RMVar_ID_23498 Human_SNP_ID_655157086 A-to-I Human chr19 + 785540 785538 785540 GGGACTACACGCGTGTGCCACCACGCCAGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTTG GGGACTACACGCGTGTGCCACCACGCCAGGC__ATTTTTGTATTTTTAGTAGAGACGGGGTTTTG CTA C LINC01836 Ensembl:ENSG00000267530 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1356944852 Functional Loss DEL dbSNP153 32..33 33 - - - Human_Splice_Rec_1928940 23499 RMVar_ID_23499 Human_SNP_ID_655157088 A-to-I Human chr19 + 785540 785540 785540 GGGACTACACGCGTGTGCCACCACGCCAGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTTG GGGACTACACGCGTGTGCCACCACGCCAGGCTGATTTTTGTATTTTTAGTAGAGACGGGGTTTTG A G LINC01836 Ensembl:ENSG00000267530 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1052253248 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1928940 23500 RMVar_ID_23500 Human_SNP_ID_655157180 A-to-I Human chr19 + 785910 785910 785910 AGTGAACCCTCATCTCTACTAAAACTACAAAAAATTAGCCAGGTGTGGTGGCGGGCGCCTGTAAT AGTGAACCCTCATCTCTACTAAAACTACAAAAGATTAGCCAGGTGTGGTGGCGGGCGCCTGTAAT A G LINC01836 Ensembl:ENSG00000267530 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs953806682 Functional Loss SNV dbSNP153 33..33 33 - - - 23501 RMVar_ID_23501 Human_SNP_ID_655157185 A-to-I Human chr19 + 785918 785918 785918 CTCATCTCTACTAAAACTACAAAAAATTAGCCAGGTGTGGTGGCGGGCGCCTGTAATCCCAGCTA CTCATCTCTACTAAAACTACAAAAAATTAGCCTGGTGTGGTGGCGGGCGCCTGTAATCCCAGCTA A T LINC01836 Ensembl:ENSG00000267530 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1222905590 Functional Loss SNV dbSNP153 33..33 33 - - - 23502 RMVar_ID_23502 Human_SNP_ID_655157514 A-to-I Human chr19 + 786716 786716 786716 TTGGGAGGCCGAGGCAGGTGGATCACTAGGTCAGGAGTTTGAGACCATCCTGGCCAACATGGAGA TTGGGAGGCCGAGGCAGGTGGATCACTAGGTCGGGAGTTTGAGACCATCCTGGCCAACATGGAGA A G lnc-PTBP1-2,lnc-PTBP1-2:2 RNACentral:URS000030C0E9,RNACentral:URS00008B9CD1 lincRNA,lincRNA exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1226202284 Functional Loss SNV dbSNP153 33..33 33 - - - 23503 RMVar_ID_23503 Human_SNP_ID_655157528 A-to-I Human chr19 + 786761 786761 786761 CATCCTGGCCAACATGGAGACACCTCATCTCTACTAAAAATACAAAAATTATCTGGGCGTGGCGG CATCCTGGCCAACATGGAGACACCTCATCTCTGCTAAAAATACAAAAATTATCTGGGCGTGGCGG A G lnc-PTBP1-2,lnc-PTBP1-2:2 RNACentral:URS000030C0E9,RNACentral:URS00008B9CD1 lincRNA,lincRNA exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1239404395 Functional Loss SNV dbSNP153 33..33 33 - - - 23504 RMVar_ID_23504 Human_SNP_ID_655157543 A-to-I Human chr19 + 786811 786811 786811 ATCTGGGCGTGGCGGTGGGCGCCTGTAATCCCAGCTACTTGTGAGGCTGAAGCAGGAGAATCGCT ATCTGGGCGTGGCGGTGGGCGCCTGTAATCCCGGCTACTTGTGAGGCTGAAGCAGGAGAATCGCT A G lnc-PTBP1-2,lnc-PTBP1-2:2 RNACentral:URS000030C0E9,RNACentral:URS00008B9CD1 lincRNA,lincRNA exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1330718091 Functional Loss SNV dbSNP153 33..33 33 - - - 23505 RMVar_ID_23505 Human_SNP_ID_655157776 A-to-I Human chr19 + 787388 787388 787388 TTTTATCTTTCTTTTCCTATTTATTTAGAGACAGGGTTTCGCCATGTTGCCCAGGCTGGTCTGAA TTTTATCTTTCTTTTCCTATTTATTTAGAGACGGGGTTTCGCCATGTTGCCCAGGCTGGTCTGAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928841371 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13533194 23506 RMVar_ID_23506 Human_SNP_ID_655158025 A-to-I Human chr19 + 788174 788174 788174 CTGGCTCACTGCAACCTCTGCCTCTCGGGCTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGC CTGGCTCACTGCAACCTCTGCCTCTCGGGCTCGAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1438469196 Functional Loss SNV dbSNP153 33..33 33 - - - 23507 RMVar_ID_23507 Human_SNP_ID_655158156 A-to-I Human chr19 + 788452 788452 788452 TCACCCAGGCTGGAGTGCAGTGGCGTGATCTCAGCTCACTGCAACCTCCGCCTCTTGGGTTCAAA TCACCCAGGCTGGAGTGCAGTGGCGTGATCTCGGCTCACTGCAACCTCCGCCTCTTGGGTTCAAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1175488031 Functional Loss SNV dbSNP153 33..33 33 - - - 23508 RMVar_ID_23508 Human_SNP_ID_655159002 A-to-I Human chr19 + 790866 790866 790866 GAAACCCCATCTCTACTAAAAATACAAAAATTAGCTGGGCTTGGTGGTGGGTGCCTGCAATCTCA GAAACCCCATCTCTACTAAAAATACAAAAATTTGCTGGGCTTGGTGGTGGGTGCCTGCAATCTCA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1192418466 Functional Loss SNV dbSNP153 33..33 33 - - - 23509 RMVar_ID_23509 Human_SNP_ID_655159009 A-to-I Human chr19 + 790892 790892 790892 AAAATTAGCTGGGCTTGGTGGTGGGTGCCTGCAATCTCAGCTCCTTGGGACTCTGAGGCAGGAGA AAAATTAGCTGGGCTTGGTGGTGGGTGCCTGCGATCTCAGCTCCTTGGGACTCTGAGGCAGGAGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1201785582 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2572377 23510 RMVar_ID_23510 Human_SNP_ID_655159019 A-to-I Human chr19 + 790933 790933 790933 TCCTTGGGACTCTGAGGCAGGAGAATTGATTGAACCAGGAGGCAGAGGTTGCAGTGAACTGAGAT TCCTTGGGACTCTGAGGCAGGAGAATTGATTGTACCAGGAGGCAGAGGTTGCAGTGAACTGAGAT A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1227364921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2572378 23511 RMVar_ID_23511 Human_SNP_ID_655167310 A-to-I Human chr19 + 809126 809126 809126 CGCCTCTTGGGTTCAAGTGATTGTGCCACCTCAGCTTCCCGAGTAGCTGGGACTGTAGGCACCCA CGCCTCTTGGGTTCAAGTGATTGTGCCACCTCCGCTTCCCGAGTAGCTGGGACTGTAGGCACCCA A C PTBP1 Ensembl:ENSG00000011304 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1406818842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13535170 RMVar_hsa_circ_27836,RMVar_hsa_circ_98340,RMVar_hsa_circ_190918,RMVar_hsa_circ_31535,RMVar_hsa_circ_1756 23512 RMVar_ID_23512 Human_SNP_ID_655167339 A-to-I Human chr19 + 809174 809174 809174 GGGACTGTAGGCACCCACAACCACACCTGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCA GGGACTGTAGGCACCCACAACCACACCTGGCTCATTTTTGTATTTTTAGTAGAGACGGGGTTTCA A C PTBP1 Ensembl:ENSG00000011304 Protein coding intron GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-Seq:(High) rs1321048375 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27836,RMVar_hsa_circ_98340,RMVar_hsa_circ_190918,RMVar_hsa_circ_31535,RMVar_hsa_circ_1756 23513 RMVar_ID_23513 Human_SNP_ID_655167786 A-to-I Human chr19 + 810186 810186 810186 AAAATTAGCCTGGCATGGTGTTGCGTGCCTGTAATCCCAGCTACTTGGGAGACTGAGGCAGGAGA AAAATTAGCCTGGCATGGTGTTGCGTGCCTGTCATCCCAGCTACTTGGGAGACTGAGGCAGGAGA A C PTBP1 Ensembl:ENSG00000011304 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1319636398 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8496908 RMVar_hsa_circ_27836,RMVar_hsa_circ_98340,RMVar_hsa_circ_190918,RMVar_hsa_circ_31535,RMVar_hsa_circ_1756 23514 RMVar_ID_23514 Human_SNP_ID_655191430 A-to-I Human chr19 + 864538 864538 864538 CTGATGGGCCAGGCGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCAG CTGATGGGCCAGGCGCGGTGGCTCATGCCTGTCATCCCAGCACTTTGGGAGGCCGAGGCGGGCAG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1262422372 Functional Loss SNV dbSNP153 33..33 33 - - - 23515 RMVar_ID_23515 Human_SNP_ID_655192106 A-to-I Human chr19 + 865649 865649 865649 TCCATGTTGGTCAGGCTGGTCTCGAACTTCCGACCTCAGGTGATCCGCCCCCCCTCGGCCTCCCA TCCATGTTGGTCAGGCTGGTCTCGAACTTCCGGCCTCAGGTGATCCGCCCCCCCTCGGCCTCCCA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560456355 Functional Loss SNV dbSNP153 33..33 33 - - - 23516 RMVar_ID_23516 Human_SNP_ID_655192168 A-to-I Human chr19 + 865764 865764 865764 TTTTAAGATTTTTGTAGAGATGAGGTCTCGCCATGTTGCCCCAGGTTGGTCTTGAACTCCCAGGC TTTTAAGATTTTTGTAGAGATGAGGTCTCGCCCTGTTGCCCCAGGTTGGTCTTGAACTCCCAGGC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1045009339 Functional Loss SNV dbSNP153 33..33 33 - - - 23517 RMVar_ID_23517 Human_SNP_ID_655211332 A-to-I Human chr19 - 900897 900897 900897 CTCCGGGGAGGAGCAGGAGCGGGTTCTTCGCTACCTGGAGGATGAGGGCAGGAGCAAGGCGCGGA CTCCGGGGAGGAGCAGGAGCGGGTTCTTCGCTTCCTGGAGGATGAGGGCAGGAGCAAGGCGCGGA T A R3HDM4 Ensembl:ENSG00000198858 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs748455024 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3953882,Human_RBP_ID_4555991,Human_RBP_ID_18995591,Human_RBP_ID_27562974 Human_Splice_Rec_1929532,Human_Splice_Rec_1929533,Human_Splice_Rec_1929544,Human_Splice_Rec_1929545,Human_Splice_Rec_1929558,Human_Splice_Rec_1929559,Human_Splice_Rec_1929572,Human_Splice_Rec_1929573,Human_Splice_Rec_1929581,Human_Splice_Rec_1929590,Human_Splice_Rec_1929591 RMVar_hsa_circ_14286,RMVar_hsa_circ_70970,RMVar_hsa_circ_37602,RMVar_hsa_circ_4432 23518 RMVar_ID_23518 Human_SNP_ID_655212577 A-to-I Human chr19 - 904045 904045 904045 TTACGGTTTTTTGTTTGTTTGGCTTTTGAGACAGAGTCTCGCTCTGTCGTCCAGGCTGGAGCGCA TTACGGTTTTTTGTTTGTTTGGCTTTTGAGACGGAGTCTCGCTCTGTCGTCCAGGCTGGAGCGCA T C R3HDM4 Ensembl:ENSG00000198858 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs573123655 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13538246 23519 RMVar_ID_23519 Human_SNP_ID_655229121 A-to-I Human chr19 + 949570 949570 949570 GGCCTCAAGCCATCCTCCTGCCTCGGCCTCCCAAAGTGCTGGGATTATAGGCAGGAGCCGCCGCC GGCCTCAAGCCATCCTCCTGCCTCGGCCTCCCGAAGTGCTGGGATTATAGGCAGGAGCCGCCGCC A G ARID3A Ensembl:ENSG00000116017 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1307557893 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77808,RMVar_hsa_circ_190926 23520 RMVar_ID_23520 Human_SNP_ID_655229530 A-to-I Human chr19 + 950952 950952 950952 TCAAACTATTCTCCTGCCTCAGCCTCTTGAGTAGCTGGGGTTACGGGCATGCACCACCACGCCTG TCAAACTATTCTCCTGCCTCAGCCTCTTGAGTGGCTGGGGTTACGGGCATGCACCACCACGCCTG A G ARID3A Ensembl:ENSG00000116017 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1257969277 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77808,RMVar_hsa_circ_190926 23521 RMVar_ID_23521 Human_SNP_ID_655235441 A-to-I Human chr19 + 968930 968930 968930 CCTGCCTCGGCGTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCACCCAGCCAATCCCAGC CCTGCCTCGGCGTCCCAAAGTGCTGGGATTACGGGCGTGAGCCACCGCACCCAGCCAATCCCAGC A G ARID3A Ensembl:ENSG00000116017 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1239959776 Functional Loss SNV dbSNP153 33..33 33 - - - 23522 RMVar_ID_23522 Human_SNP_ID_655235542 A-to-I Human chr19 + 969335 969335 969335 AACACGGGAGGATCACTTGAGCCCAGGAGTTCAAGACCAGTCTGGGCAACATAGTGAGACCCCAT AACACGGGAGGATCACTTGAGCCCAGGAGTTCGAGACCAGTCTGGGCAACATAGTGAGACCCCAT A G ARID3A Ensembl:ENSG00000116017 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1292010207 Functional Loss SNV dbSNP153 33..33 33 - - - 23523 RMVar_ID_23523 Human_SNP_ID_655235549 A-to-I Human chr19 + 969355 969355 969355 GCCCAGGAGTTCAAGACCAGTCTGGGCAACATAGTGAGACCCCATCTCTCCTAAAAATATAAAAA GCCCAGGAGTTCAAGACCAGTCTGGGCAACATGGTGAGACCCCATCTCTCCTAAAAATATAAAAA A G ARID3A Ensembl:ENSG00000116017 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs947357962 Functional Loss SNV dbSNP153 33..33 33 - - - 23524 RMVar_ID_23524 Human_SNP_ID_655235729 A-to-I Human chr19 + 969846 969846 969846 AAGTAGCTGGGACTACAGGCGTGTGTCACCACACCCAGCTAATTTTTTTTTGTATTTTTAGTAGA AAGTAGCTGGGACTACAGGCGTGTGTCACCACGCCCAGCTAATTTTTTTTTGTATTTTTAGTAGA A G ARID3A Ensembl:ENSG00000116017 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1262745213 Functional Loss SNV dbSNP153 33..33 33 - - - 23525 RMVar_ID_23525 Human_SNP_ID_655235958 A-to-I Human chr19 + 970563 970563 970563 AGAGTCTCACTCTGTTGCCCAGGCTGGAGTGCAATGGCATGATCTCAGCTCCTGCAACCTCCGCC AGAGTCTCACTCTGTTGCCCAGGCTGGAGTGCCATGGCATGATCTCAGCTCCTGCAACCTCCGCC A C ARID3A Ensembl:ENSG00000116017 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs113658909 Functional Loss SNV dbSNP153 33..33 33 - - - 23526 RMVar_ID_23526 Human_SNP_ID_655235959 A-to-I Human chr19 + 970563 970563 970563 AGAGTCTCACTCTGTTGCCCAGGCTGGAGTGCAATGGCATGATCTCAGCTCCTGCAACCTCCGCC AGAGTCTCACTCTGTTGCCCAGGCTGGAGTGCGATGGCATGATCTCAGCTCCTGCAACCTCCGCC A G ARID3A Ensembl:ENSG00000116017 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs113658909 Functional Loss SNV dbSNP153 33..33 33 - - - 23527 RMVar_ID_23527 Human_SNP_ID_655235979 A-to-I Human chr19 + 970640 970640 970640 GGGATTACAGGTGCATGCCACCAGGCCCGGCTAATTTTTGTATTTTTAGATGATACGGGGTTTCA GGGATTACAGGTGCATGCCACCAGGCCCGGCTTATTTTTGTATTTTTAGATGATACGGGGTTTCA A T ARID3A Ensembl:ENSG00000116017 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs546248507 Functional Loss SNV dbSNP153 33..33 33 - - - 23528 RMVar_ID_23528 Human_SNP_ID_655245259 A-to-I Human chr19 + 996942 996942 996942 CAGGCTGGAGTGCAGTGGCCCGGTCTCCGTTCACTGCAACTTCTGCCTCCCGGGTTCATGCCATT CAGGCTGGAGTGCAGTGGCCCGGTCTCCGTTCCCTGCAACTTCTGCCTCCCGGGTTCATGCCATT A C WDR18 Ensembl:ENSG00000065268 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1400395834 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27473180 23529 RMVar_ID_23529 Human_SNP_ID_655245260 A-to-I Human chr19 + 996942 996942 996942 CAGGCTGGAGTGCAGTGGCCCGGTCTCCGTTCACTGCAACTTCTGCCTCCCGGGTTCATGCCATT CAGGCTGGAGTGCAGTGGCCCGGTCTCCGTTCGCTGCAACTTCTGCCTCCCGGGTTCATGCCATT A G WDR18 Ensembl:ENSG00000065268 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1400395834 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27473180 23530 RMVar_ID_23530 Human_SNP_ID_655248795 A-to-I Human chr19 - 1006002 1006002 1006002 TCTGTGTTTTTTGTTTTGTTTTTTGTTTTTTGAGACGGAGTCTTGCTCTGTTGCCCAGGCTAGAG TCTGTGTTTTTTGTTTTGTTTTTTGTTTTTTGCGACGGAGTCTTGCTCTGTTGCCCAGGCTAGAG T G lnc-TMEM259-1 RNACentral:URS00008BAF45 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202458404 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3562078 23531 RMVar_ID_23531 Human_SNP_ID_655259105 A-to-I Human chr19 + 1032107 1032107 1032107 AAAATTAGCCGGGTGTGGTGGCAGGCACCTGTAATCCCAGCTACTCGGGAGGCTCAGGGCTGAGG AAAATTAGCCGGGTGTGGTGGCAGGCACCTGTTATCCCAGCTACTCGGGAGGCTCAGGGCTGAGG A T CNN2 Ensembl:ENSG00000064666 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs542810642 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108455,RMVar_hsa_circ_116004,RMVar_hsa_circ_127267,RMVar_hsa_circ_190944,RMVar_hsa_circ_99991,RMVar_hsa_circ_190943,RMVar_hsa_circ_274562,RMVar_hsa_circ_125242,RMVar_hsa_circ_190945,RMVar_hsa_circ_80000,RMVar_hsa_circ_82365,RMVar_hsa_circ_190947,RMVar_hsa_circ_190949,RMVar_hsa_circ_190950,RMVar_hsa_circ_190948,RMVar_hsa_circ_190946 23532 RMVar_ID_23532 Human_SNP_ID_655259500 A-to-I Human chr19 + 1033256 1033256 1033256 TATGTAAGCTCTGGCCGGGCGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGT TATGTAAGCTCTGGCCGGGCGCAGTGGCTCACCCCTGTAATCCCAGCACTTTGGGAGGCCGAGGT A C CNN2 Ensembl:ENSG00000064666 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1050748022 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3582040 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 23533 RMVar_ID_23533 Human_SNP_ID_655260162 A-to-I Human chr19 + 1035667 1035667 1035667 CCCATGGGCTGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTTGGAGGTTGAGGCGGGTGG CCCATGGGCTGGGCGCGGTGGCTCACGCCTGTGATCCCAGCACTTTTGGAGGTTGAGGCGGGTGG A G CNN2 Ensembl:ENSG00000064666 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037220159 Functional Loss SNV dbSNP153 33..33 33 - - - 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 23534 RMVar_ID_23534 Human_SNP_ID_655260192 A-to-I Human chr19 + 1035760 1035760 1035760 GCCTGGCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCCTGGCGTGGTGGCAC GCCTGGCAACATGGTGAAACCCCGTCTCTACTTAAAATACAAAAATTAGCCTGGCGTGGTGGCAC A T CNN2 Ensembl:ENSG00000064666 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs754493143 Functional Loss SNV dbSNP153 33..33 33 - - - 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 23535 RMVar_ID_23535 Human_SNP_ID_655260198 A-to-I Human chr19 + 1035775 1035775 1035775 GAAACCCCGTCTCTACTAAAAATACAAAAATTAGCCTGGCGTGGTGGCACACGCCTGTAATCCTA GAAACCCCGTCTCTACTAAAAATACAAAAATTGGCCTGGCGTGGTGGCACACGCCTGTAATCCTA A G CNN2 Ensembl:ENSG00000064666 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs868544779 Functional Loss SNV dbSNP153 33..33 33 - - - 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 23536 RMVar_ID_23536 Human_SNP_ID_655278267 A-to-I Human chr19 + 1078526 1078526 1078526 GTGGTGAGATCTCACTGCAACCTCCGCCTCCCAGGTTCACACAGTTCTCTGCCTCAGCCACCCTG GTGGTGAGATCTCACTGCAACCTCCGCCTCCCGGGTTCACACAGTTCTCTGCCTCAGCCACCCTG A G ARHGAP45 Ensembl:ENSG00000180448 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1192832340 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80377,RMVar_hsa_circ_85872,RMVar_hsa_circ_190975,RMVar_hsa_circ_190976 23537 RMVar_ID_23537 Human_SNP_ID_655278286 A-to-I Human chr19 + 1078600 1078600 1078600 CCAGCTAATTTTTTTGTATTTTTAGTAGACACAGAGTTTCACCATCTTGGCCAGGTTGGTCTCAA CCAGCTAATTTTTTTGTATTTTTAGTAGACACGGAGTTTCACCATCTTGGCCAGGTTGGTCTCAA A G ARHGAP45 Ensembl:ENSG00000180448 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1325482143 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80377,RMVar_hsa_circ_85872,RMVar_hsa_circ_190975,RMVar_hsa_circ_190976 23538 RMVar_ID_23538 Human_SNP_ID_655278548 A-to-I Human chr19 + 1079388 1079388 1079388 TTAACCGGGTATGGTGGGTGGGGGGCACCTGTAATCCGTTACTTGGGAGGCTGAGGCAGAATTGC TTAACCGGGTATGGTGGGTGGGGGGCACCTGTCATCCGTTACTTGGGAGGCTGAGGCAGAATTGC A C ARHGAP45 Ensembl:ENSG00000180448 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1249120612 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80377,RMVar_hsa_circ_85872,RMVar_hsa_circ_190975,RMVar_hsa_circ_190976 23539 RMVar_ID_23539 Human_SNP_ID_655282619 A-to-I Human chr19 - 1087270 1087270 1087270 TGCATGCCTGTAATCCCAGCTACTTGGGAGCTAAGGCAGGAGAATCACTTGAACCCAGGAAGTGG TGCATGCCTGTAATCCCAGCTACTTGGGAGCTGAGGCAGGAGAATCACTTGAACCCAGGAAGTGG T C POLR2E Ensembl:ENSG00000099817 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1451341893 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1553984,Human_RBP_ID_13361180,Human_RBP_ID_25381954 RMVar_hsa_circ_84576,RMVar_hsa_circ_96904,RMVar_hsa_circ_190977,RMVar_hsa_circ_190978 23540 RMVar_ID_23540 Human_SNP_ID_655287874 A-to-I Human chr19 - 1099769 1099769 1099769 TCTCAGCCTCCTGAATAGCTGAGATTACAGGCATGCGCCACCATGCCCGGCTATGGGCTGTTTTC TCTCAGCCTCCTGAATAGCTGAGATTACAGGCCTGCGCCACCATGCCCGGCTATGGGCTGTTTTC T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs895684435 Functional Loss SNV dbSNP153 33..33 33 - - - 23541 RMVar_ID_23541 Human_SNP_ID_655391129 A-to-I Human chr19 + 1374764 1374764 1374764 TCATACTCTTTCGTAAAAAATTATTTTTAGTCAGTCACAGTGGCTCATGCCTGTAATCCCAGCAC TCATACTCTTTCGTAAAAAATTATTTTTAGTCCGTCACAGTGGCTCATGCCTGTAATCCCAGCAC A C PWWP3A Ensembl:ENSG00000160953 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1269420702 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13373868 23542 RMVar_ID_23542 Human_SNP_ID_655391241 A-to-I Human chr19 + 1375108 1375108 1375108 AAGCATGGTGGCACGCGCCTATAGTCAGTCCCAGCTACTCAGCAGGCTGAGGCAGGGGAATCGCT AAGCATGGTGGCACGCGCCTATAGTCAGTCCCGGCTACTCAGCAGGCTGAGGCAGGGGAATCGCT A G PWWP3A Ensembl:ENSG00000160953 Protein coding intron GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs1380485674 Functional Loss SNV dbSNP153 33..33 33 - - - 23543 RMVar_ID_23543 Human_SNP_ID_655391854 A-to-I Human chr19 + 1375869 1375869 1375869 GCTCTGTCACCCAGGCTGGAGTGCAGTGGCACAGTCTCGGCCCACTGCAACCCCCCCACCGTGCC GCTCTGTCACCCAGGCTGGAGTGCAGTGGCACGGTCTCGGCCCACTGCAACCCCCCCACCGTGCC A G PWWP3A Ensembl:ENSG00000160953 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1188032773 Functional Loss SNV dbSNP153 33..33 33 - - - 23544 RMVar_ID_23544 Human_SNP_ID_655391891 A-to-I Human chr19 + 1375927 1375912 1375928 CCGTGCCTTGGTTCAAGCGATTCTTCTGACTCAGCCTCCCGAGTGGCTAGGATTGCAGGTGCCCA CCGTGCCTTGGTTCAAGC________________CCTCCCGAGTGGCTAGGATTGCAGGTGCCCA CGATTCTTCTGACTCAG C PWWP3A Ensembl:ENSG00000160953 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1555773500 Functional Loss DEL dbSNP153 19..34 33 - - - Human_RBP_ID_27463878 23545 RMVar_ID_23545 Human_SNP_ID_655392032 A-to-I Human chr19 + 1376225 1376211 1376226 TTGGCTCACTGCAAGCACCACCTCCCGGTTTCAAGCGATTCTCCTACCTCAGCCTCCTAAGTAGC TTGGCTCACTGCAAGCACC_______________GCGATTCTCCTACCTCAGCCTCCTAAGTAGC CACCTCCCGGTTTCAA C PWWP3A Ensembl:ENSG00000160953 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs551967270 Functional Loss DEL dbSNP153 20..34 33 - - - 23546 RMVar_ID_23546 Human_SNP_ID_655392052 A-to-I Human chr19 + 1376243 1376243 1376243 CACCTCCCGGTTTCAAGCGATTCTCCTACCTCAGCCTCCTAAGTAGCTGGGATTACAGACATGCG CACCTCCCGGTTTCAAGCGATTCTCCTACCTCTGCCTCCTAAGTAGCTGGGATTACAGACATGCG A T PWWP3A Ensembl:ENSG00000160953 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs928163866 Functional Loss SNV dbSNP153 33..33 33 - - - 23547 RMVar_ID_23547 Human_SNP_ID_655411419 A-to-I Human chr19 + 1430265 1430261 1430265 CCGCCCCCTGCAGGAAGAGGAGCCCCCCCGCCACCCCCACCGTTCACCTCCTACATCGTGTCCAC CCGCCCCCTGCAGGAAGAGGAGCCCCCCC____CCCCCACCGTTCACCTCCTACATCGTGTCCAC CGCCA C DAZAP1 Ensembl:ENSG00000071626 Protein coding CDS GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs753877838 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_514243 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_2147293,Human_miRNA_ID_2988720,Human_miRNA_ID_3022419,Human_miRNA_ID_3096592 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 23548 RMVar_ID_23548 Human_SNP_ID_655411422 A-to-I Human chr19 + 1430265 1430264 1430265 CCGCCCCCTGCAGGAAGAGGAGCCCCCCCGCCACCCCCACCGTTCACCTCCTACATCGTGTCCAC CCGCCCCCTGCAGGAAGAGGAGCCCCCCCGCC_CCCCCACCGTTCACCTCCTACATCGTGTCCAC CA C DAZAP1 Ensembl:ENSG00000071626 Protein coding CDS GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1388829468 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_514243 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_2147293,Human_miRNA_ID_2988720,Human_miRNA_ID_3022419,Human_miRNA_ID_3096592 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 23549 RMVar_ID_23549 Human_SNP_ID_655411423 A-to-I Human chr19 + 1430265 1430265 1430265 CCGCCCCCTGCAGGAAGAGGAGCCCCCCCGCCACCCCCACCGTTCACCTCCTACATCGTGTCCAC CCGCCCCCTGCAGGAAGAGGAGCCCCCCCGCCCCCCCCACCGTTCACCTCCTACATCGTGTCCAC A C DAZAP1 Ensembl:ENSG00000071626 Protein coding CDS GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs760070630 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_514243 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_2147293,Human_miRNA_ID_2988720,Human_miRNA_ID_3022419,Human_miRNA_ID_3096592 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 23550 RMVar_ID_23550 Human_SNP_ID_655421978 A-to-I Human chr19 - 1458517 1458517 1458517 TTTTGCCCAGCCTGGTCTCGAACTTCTGAGCTAAAGTCATCCTCCTGCCTTGGCCTCCCAAACTG TTTTGCCCAGCCTGGTCTCGAACTTCTGAGCTGAAGTCATCCTCCTGCCTTGGCCTCCCAAACTG T C AC027307.2 Ensembl:ENSG00000267317 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs987471819 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4505692,Human_RBP_ID_13377443,Human_RBP_ID_17915917,Human_RBP_ID_23174420,Human_RBP_ID_26471563,Human_RBP_ID_27464185 23551 RMVar_ID_23551 Human_SNP_ID_655421986 A-to-I Human chr19 - 1458554 1458554 1458554 GACTAATTTTTTTTTTGTAGTGATGGGGTCTCACTATTTTTGCCCAGCCTGGTCTCGAACTTCTG GACTAATTTTTTTTTTGTAGTGATGGGGTCTCGCTATTTTTGCCCAGCCTGGTCTCGAACTTCTG T C AC027307.2 Ensembl:ENSG00000267317 lincRNA exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1165764195 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2557308,Human_RBP_ID_13377444,Human_RBP_ID_26471563 23552 RMVar_ID_23552 Human_SNP_ID_655421990 A-to-I Human chr19 - 1458568 1458568 1458568 TCCCCAGTAGCTGGGACTAATTTTTTTTTTGTAGTGATGGGGTCTCACTATTTTTGCCCAGCCTG TCCCCAGTAGCTGGGACTAATTTTTTTTTTGTGGTGATGGGGTCTCACTATTTTTGCCCAGCCTG T C AC027307.2 Ensembl:ENSG00000267317 lincRNA exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs140712583 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26471563 23553 RMVar_ID_23553 Human_SNP_ID_655422020 A-to-I Human chr19 - 1458698 1458698 1458698 AAAAGTTACAGCAAGACTTTTCTTTTTGAGACAGGGTCTGGCTCTGTTGCCCAGTCTGGAGTGTG AAAAGTTACAGCAAGACTTTTCTTTTTGAGACGGGGTCTGGCTCTGTTGCCCAGTCTGGAGTGTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1384330238 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17266831,Human_RBP_ID_27464186 23554 RMVar_ID_23554 Human_SNP_ID_655432949 A-to-I Human chr19 - 1484296 1484296 1484296 TTTTGTAGAGTTGGGGTTTCACTATGTTGACCAGGCTGGTCTTGAACTCCTGACCTCAGACAACA TTTTGTAGAGTTGGGGTTTCACTATGTTGACCTGGCTGGTCTTGAACTCCTGACCTCAGACAACA T A PCSK4 Ensembl:ENSG00000115257 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1262034196 Functional Loss SNV dbSNP153 33..33 33 - - - 23555 RMVar_ID_23555 Human_SNP_ID_655466049 A-to-I Human chr19 - 1574129 1574129 1574129 CACCCCCAGTAGAGACGGGGTTTCACCATGTTAGCCAGGCTGGTCACGAACTCCTGACCTCAAGT CACCCCCAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGGTCACGAACTCCTGACCTCAAGT T C MBD3 Ensembl:ENSG00000071655 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs914520134 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13383367 23556 RMVar_ID_23556 Human_SNP_ID_655469082 A-to-I Human chr19 - 1582033 1582033 1582033 GCCAGGTGCAGTGGCTCACGCCTGTAATCCCAACACTCTGGGAGGCCAAGGCGGGCGGATCATGA GCCAGGTGCAGTGGCTCACGCCTGTAATCCCAGCACTCTGGGAGGCCAAGGCGGGCGGATCATGA T C MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1005090483 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_46920,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_81198,RMVar_hsa_circ_191101 23557 RMVar_ID_23557 Human_SNP_ID_655469128 A-to-I Human chr19 - 1582177 1582177 1582177 ACAGGGTCGGCTGGGTACAGTGGCTCACACCTATAATCCCAGCACTTGGCGGGGCTGGGGCAGGA ACAGGGTCGGCTGGGTACAGTGGCTCACACCTGTAATCCCAGCACTTGGCGGGGCTGGGGCAGGA T C MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1205695297 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239154,Human_RBP_ID_770043,Human_RBP_ID_824113,Human_RBP_ID_22809658,Human_RBP_ID_25387194 RMVar_hsa_circ_46920,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_81198,RMVar_hsa_circ_191101 23558 RMVar_ID_23558 Human_SNP_ID_655470686 A-to-I Human chr19 - 1586533 1586533 1586533 TTGCATTCCAGCCTGGGCAAGAGTGAGACCCTATCTCCAAAAGGAAAGAGAGAAACGAAGTCCTG TTGCATTCCAGCCTGGGCAAGAGTGAGACCCTGTCTCCAAAAGGAAAGAGAGAAACGAAGTCCTG T C MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1322758472 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_514916,Human_RBP_ID_6724409,Human_RBP_ID_13383606,Human_RBP_ID_17934769,Human_RBP_ID_23174588,Human_RBP_ID_25387204,Human_RBP_ID_26473091 RMVar_hsa_circ_86392,RMVar_hsa_circ_191099 23559 RMVar_ID_23559 Human_SNP_ID_655470716 A-to-I Human chr19 - 1586606 1586606 1586606 TACTTGGGAGACTAAGGTGGAAGGATCACCCTAGCCCAGGAGTTCAAGGTTGCAGTGAGCTGTGA TACTTGGGAGACTAAGGTGGAAGGATCACCCTGGCCCAGGAGTTCAAGGTTGCAGTGAGCTGTGA T C MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs979614892 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8478816,Human_RBP_ID_13383608,Human_RBP_ID_17694754,Human_RBP_ID_17916320 RMVar_hsa_circ_86392,RMVar_hsa_circ_191099 23560 RMVar_ID_23560 Human_SNP_ID_655470781 A-to-I Human chr19 - 1586769 1586769 1586769 CCAGCTACTCAGGAGGCTCAGGCAGGAGAATCACTTGAACCTGGGAGGTGGAGGTTGCAGAGAGC CCAGCTACTCAGGAGGCTCAGGCAGGAGAATCGCTTGAACCTGGGAGGTGGAGGTTGCAGAGAGC T C MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs967398797 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25387211 RMVar_hsa_circ_86392,RMVar_hsa_circ_191099 23561 RMVar_ID_23561 Human_SNP_ID_655470783 A-to-I Human chr19 - 1586773 1586773 1586773 ACTCCCAGCTACTCAGGAGGCTCAGGCAGGAGAATCACTTGAACCTGGGAGGTGGAGGTTGCAGA ACTCCCAGCTACTCAGGAGGCTCAGGCAGGAGGATCACTTGAACCTGGGAGGTGGAGGTTGCAGA T C MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs926096608 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86392,RMVar_hsa_circ_191099 23562 RMVar_ID_23562 Human_SNP_ID_655470787 A-to-I Human chr19 - 1586791 1586791 1586791 GTGGTGGCGGGCACCTGTACTCCCAGCTACTCAGGAGGCTCAGGCAGGAGAATCACTTGAACCTG GTGGTGGCGGGCACCTGTACTCCCAGCTACTCGGGAGGCTCAGGCAGGAGAATCACTTGAACCTG T C MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs917469657 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86392,RMVar_hsa_circ_191099 23563 RMVar_ID_23563 Human_SNP_ID_655470807 A-to-I Human chr19 - 1586866 1586866 1586866 GGTCAGGAGTTCGTGACCAGCCTGGCCAACACAGTGAAACCTGGTCTCTACTAAAAATACAAAAA GGTCAGGAGTTCGTGACCAGCCTGGCCAACACGGTGAAACCTGGTCTCTACTAAAAATACAAAAA T C MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1322235474 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86392,RMVar_hsa_circ_191099 23564 RMVar_ID_23564 Human_SNP_ID_655470808 A-to-I Human chr19 - 1586868 1586868 1586868 GAGGTCAGGAGTTCGTGACCAGCCTGGCCAACACAGTGAAACCTGGTCTCTACTAAAAATACAAA GAGGTCAGGAGTTCGTGACCAGCCTGGCCAACGCAGTGAAACCTGGTCTCTACTAAAAATACAAA T C MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs886762842 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86392,RMVar_hsa_circ_191099 23565 RMVar_ID_23565 Human_SNP_ID_655470874 A-to-I Human chr19 - 1587055 1587055 1587055 AGGCTGAGTCAGGAGAATGGTGTGAACCCGGAAGTCGGAGGTTGCAGTGAGCCAAGATCGCACCA AGGCTGAGTCAGGAGAATGGTGTGAACCCGGACGTCGGAGGTTGCAGTGAGCCAAGATCGCACCA T G MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs940986900 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13383611 RMVar_hsa_circ_86392,RMVar_hsa_circ_191099 23566 RMVar_ID_23566 Human_SNP_ID_655470877 A-to-I Human chr19 - 1587062 1587062 1587062 ACTCGGGAGGCTGAGTCAGGAGAATGGTGTGAACCCGGAAGTCGGAGGTTGCAGTGAGCCAAGAT ACTCGGGAGGCTGAGTCAGGAGAATGGTGTGAGCCCGGAAGTCGGAGGTTGCAGTGAGCCAAGAT T C MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs932438226 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13383611 RMVar_hsa_circ_86392,RMVar_hsa_circ_191099 23567 RMVar_ID_23567 Human_SNP_ID_655470880 A-to-I Human chr19 - 1587071 1587071 1587071 GTCCCAGCTACTCGGGAGGCTGAGTCAGGAGAATGGTGTGAACCCGGAAGTCGGAGGTTGCAGTG GTCCCAGCTACTCGGGAGGCTGAGTCAGGAGAGTGGTGTGAACCCGGAAGTCGGAGGTTGCAGTG T C MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1366877972 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13383611 RMVar_hsa_circ_86392,RMVar_hsa_circ_191099 23568 RMVar_ID_23568 Human_SNP_ID_655470891 A-to-I Human chr19 - 1587104 1587104 1587104 AAAATTAGCCGGGCGTGGTGGTGGGCAGCTGTAGTCCCAGCTACTCGGGAGGCTGAGTCAGGAGA AAAATTAGCCGGGCGTGGTGGTGGGCAGCTGTGGTCCCAGCTACTCGGGAGGCTGAGTCAGGAGA T C MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE38233;GSE100210;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1009440654 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86392,RMVar_hsa_circ_191099 23569 RMVar_ID_23569 Human_SNP_ID_655470905 A-to-I Human chr19 - 1587130 1587130 1587130 AAACCCCACCTCTACTAAAAATATAAAAAATTAGCCGGGCGTGGTGGTGGGCAGCTGTAGTCCCA AAACCCCACCTCTACTAAAAATATAAAAAATTGGCCGGGCGTGGTGGTGGGCAGCTGTAGTCCCA T C MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs958981418 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17916321 RMVar_hsa_circ_86392,RMVar_hsa_circ_191099 23570 RMVar_ID_23570 Human_SNP_ID_655470909 A-to-I Human chr19 - 1587146 1587146 1587146 CCTGGCTAACACTGTGAAACCCCACCTCTACTAAAAATATAAAAAATTAGCCGGGCGTGGTGGTG CCTGGCTAACACTGTGAAACCCCACCTCTACTTAAAATATAAAAAATTAGCCGGGCGTGGTGGTG T A MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs982915785 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86392,RMVar_hsa_circ_191099 23571 RMVar_ID_23571 Human_SNP_ID_655470910 A-to-I Human chr19 - 1587146 1587146 1587146 CCTGGCTAACACTGTGAAACCCCACCTCTACTAAAAATATAAAAAATTAGCCGGGCGTGGTGGTG CCTGGCTAACACTGTGAAACCCCACCTCTACTGAAAATATAAAAAATTAGCCGGGCGTGGTGGTG T C MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs982915785 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86392,RMVar_hsa_circ_191099 23572 RMVar_ID_23572 Human_SNP_ID_655470972 A-to-I Human chr19 - 1587334 1587334 1587334 AGCTTTGGGAGGGAAGATGGGAGGACTGCTTGAGCTCAGGAGTTCCAGACCAGCCTGGGTAACAT AGCTTTGGGAGGGAAGATGGGAGGACTGCTTGGGCTCAGGAGTTCCAGACCAGCCTGGGTAACAT T C MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1263861515 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1292331,Human_RBP_ID_6724411,Human_RBP_ID_13383618,Human_RBP_ID_26473092 RMVar_hsa_circ_86392,RMVar_hsa_circ_191099 23573 RMVar_ID_23573 Human_SNP_ID_655471033 A-to-I Human chr19 - 1587512 1587512 1587512 TCCTCAGGAGGCCAAGGCAGGACAATCCCTTGAGTCCAGGAGGTCAAGGCTGCAGTGTGCTGTGA TCCTCAGGAGGCCAAGGCAGGACAATCCCTTGGGTCCAGGAGGTCAAGGCTGCAGTGTGCTGTGA T C MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1137912 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6724418,Human_RBP_ID_17568223,Human_RBP_ID_17916326 RMVar_hsa_circ_86392,RMVar_hsa_circ_191099 23574 RMVar_ID_23574 Human_SNP_ID_655471036 A-to-I Human chr19 - 1587526 1587526 1587526 CGTGTAGTCCTAGCTCCTCAGGAGGCCAAGGCAGGACAATCCCTTGAGTCCAGGAGGTCAAGGCT CGTGTAGTCCTAGCTCCTCAGGAGGCCAAGGCGGGACAATCCCTTGAGTCCAGGAGGTCAAGGCT T C MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1137910 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13545391,Human_RBP_ID_17568223,Human_RBP_ID_17916326,Human_RBP_ID_23174604 RMVar_hsa_circ_86392,RMVar_hsa_circ_191099 23575 RMVar_ID_23575 Human_SNP_ID_655471040 A-to-I Human chr19 - 1587539 1587539 1587539 ATGGTGGTGCACACGTGTAGTCCTAGCTCCTCAGGAGGCCAAGGCAGGACAATCCCTTGAGTCCA ATGGTGGTGCACACGTGTAGTCCTAGCTCCTCGGGAGGCCAAGGCAGGACAATCCCTTGAGTCCA T C MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1137908 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13545391,Human_RBP_ID_17568223,Human_RBP_ID_26465350 RMVar_hsa_circ_86392,RMVar_hsa_circ_191099 23576 RMVar_ID_23576 Human_SNP_ID_655471044 A-to-I Human chr19 - 1587559 1587559 1587559 AATTTAAAAATTAGCTGGGCATGGTGGTGCACACGTGTAGTCCTAGCTCCTCAGGAGGCCAAGGC AATTTAAAAATTAGCTGGGCATGGTGGTGCACGCGTGTAGTCCTAGCTCCTCAGGAGGCCAAGGC T C MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1137906 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4507228,Human_RBP_ID_13383635,Human_RBP_ID_17568223,Human_RBP_ID_26471594 RMVar_hsa_circ_86392,RMVar_hsa_circ_191099 23577 RMVar_ID_23577 Human_SNP_ID_655471052 A-to-I Human chr19 - 1587579 1587579 1587579 GAGTCCCCATCTATGCAAAAAATTTAAAAATTAGCTGGGCATGGTGGTGCACACGTGTAGTCCTA GAGTCCCCATCTATGCAAAAAATTTAAAAATTGGCTGGGCATGGTGGTGCACACGTGTAGTCCTA T C MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1137905 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13383637,Human_RBP_ID_17568223,Human_RBP_ID_17916327,Human_RBP_ID_26471594 RMVar_hsa_circ_86392,RMVar_hsa_circ_191099 23578 RMVar_ID_23578 Human_SNP_ID_655471060 A-to-I Human chr19 - 1587592 1587592 1587592 TGGGCAACATAGCGAGTCCCCATCTATGCAAAAAATTTAAAAATTAGCTGGGCATGGTGGTGCAC TGGGCAACATAGCGAGTCCCCATCTATGCAAACAATTTAAAAATTAGCTGGGCATGGTGGTGCAC T G MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE38233;GSE100210;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,31158229,32596459 RNA-Seq:(High) rs901533629 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13383638,Human_RBP_ID_17916327,Human_RBP_ID_23174605 RMVar_hsa_circ_86392,RMVar_hsa_circ_191099 23579 RMVar_ID_23579 Human_SNP_ID_655471086 A-to-I Human chr19 - 1587685 1587685 1587685 AAGACACCAGCCAGGCATAGTGGCTGCCGCCTATAATCCCTTTGGGAGGTCGAGGCAGGAGGATC AAGACACCAGCCAGGCATAGTGGCTGCCGCCTGTAATCCCTTTGGGAGGTCGAGGCAGGAGGATC T C MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-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 23580 RMVar_ID_23580 Human_SNP_ID_655471388 A-to-I Human chr19 - 1588716 1588716 1588716 GGAGTGCAGTGTCATGATCTCGGCTCACTGCAACCTCTGCCTCCTGGGTTCAACCCAATTCTGCG GGAGTGCAGTGTCATGATCTCGGCTCACTGCAGCCTCTGCCTCCTGGGTTCAACCCAATTCTGCG T C MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027508451 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6724455,Human_RBP_ID_13383709 RMVar_hsa_circ_86392,RMVar_hsa_circ_191099 23581 RMVar_ID_23581 Human_SNP_ID_655471564 A-to-I Human chr19 - 1589149 1589149 1589149 TTTTGTATTTTTAGTCGAGATGGGGTTTCACCATGTTGGTCAGGCTGGTCTCGAACTCCTGATCT TTTTGTATTTTTAGTCGAGATGGGGTTTCACCGTGTTGGTCAGGCTGGTCTCGAACTCCTGATCT T C MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs910308545 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86392,RMVar_hsa_circ_191099 23582 RMVar_ID_23582 Human_SNP_ID_655471705 A-to-I Human chr19 - 1589470 1589470 1589470 TTTTATATTTTTAATAGAGACGGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGACCT TTTTATATTTTTAATAGAGACGGGGTTTCACCTTGTTGGCCAGGCTGGTCTTGAACTCCTGACCT T A MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1419783848 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86392,RMVar_hsa_circ_191099 23583 RMVar_ID_23583 Human_SNP_ID_655471743 A-to-I Human chr19 - 1589648 1589646 1589649 TTTATGTTCATTATTATTTATTTATTTTGAGAAGTAGTCCCGCTTTGTCACCCAGGGTGGAATGC TTTATGTTCATTATTATTTATTTATTTTGAG___TAGTCCCGCTTTGTCACCCAGGGTGGAATGC ACTT A MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1226098633 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_6724476,Human_RBP_ID_8199230,Human_RBP_ID_13383756,Human_RBP_ID_17916344,Human_RBP_ID_18723824,Human_RBP_ID_23174635,Human_RBP_ID_27675010 RMVar_hsa_circ_86392,RMVar_hsa_circ_191099 23584 RMVar_ID_23584 Human_SNP_ID_655471757 A-to-I Human chr19 - 1589705 1589705 1589705 CCTAAGCCTCCAGCATAGCTGGGACTACAGGCATGTGCCACCATGCCCAGCTAATTTTTTATGTT CCTAAGCCTCCAGCATAGCTGGGACTACAGGCGTGTGCCACCATGCCCAGCTAATTTTTTATGTT T C MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs911019641 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86392,RMVar_hsa_circ_191099 23585 RMVar_ID_23585 Human_SNP_ID_655471783 A-to-I Human chr19 - 1589828 1589826 1589828 GCATTCATTCATTCATTTATTCATTGTGAGACAGGGTCTTGTTCTGTCACCCAGGCTGGAGTGCA GCATTCATTCATTCATTTATTCATTGTGAGAC__GGTCTTGTTCTGTCACCCAGGCTGGAGTGCA CCT C MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1403813087 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_1555954,Human_RBP_ID_3564004,Human_RBP_ID_6724483,Human_RBP_ID_13383773,Human_RBP_ID_17266943,Human_RBP_ID_17382289,Human_RBP_ID_17498045,Human_RBP_ID_18301819 RMVar_hsa_circ_86392,RMVar_hsa_circ_191099 23586 RMVar_ID_23586 Human_SNP_ID_655471864 A-to-I Human chr19 - 1590115 1590115 1590115 TTTTGTATTTTTAGTAGAGAAGGGGTTTCGCCATGTTGGCCAGACTGGTCTCGAACTCCTGACCC TTTTGTATTTTTAGTAGAGAAGGGGTTTCGCCGTGTTGGCCAGACTGGTCTCGAACTCCTGACCC T C MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs950349885 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13383795,Human_RBP_ID_25387265 RMVar_hsa_circ_86392,RMVar_hsa_circ_191099 23587 RMVar_ID_23587 Human_SNP_ID_655471871 A-to-I Human chr19 - 1590135 1590135 1590135 TGCCACCATGCCCGGCTAATTTTTGTATTTTTAGTAGAGAAGGGGTTTCGCCATGTTGGCCAGAC TGCCACCATGCCCGGCTAATTTTTGTATTTTTTGTAGAGAAGGGGTTTCGCCATGTTGGCCAGAC T A MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1229200176 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86392,RMVar_hsa_circ_191099 23588 RMVar_ID_23588 Human_SNP_ID_655471896 A-to-I Human chr19 - 1590198 1590198 1590198 CACCTCCCGGGTTCAAGCGATTCTTCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCGTCTG CACCTCCCGGGTTCAAGCGATTCTTCTGCCTCGGCCTCCCGAGTAGCTGGGATTACAGGCGTCTG T C MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1010393426 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86392,RMVar_hsa_circ_191099 23589 RMVar_ID_23589 Human_SNP_ID_655471945 A-to-I Human chr19 - 1590359 1590359 1590359 CCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGCCTGGCCAAAGCCACTTTTTAG CCTCAGCCTCCCAAAGTGCTGGGATTACAGGCCTGAGCCACTGCCTGGCCAAAGCCACTTTTTAG T G MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1203519895 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86392,RMVar_hsa_circ_191099 23590 RMVar_ID_23590 Human_SNP_ID_655471951 A-to-I Human chr19 - 1590387 1590387 1590387 GAATTCCTGGACTCAAGCAGTTAACCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAG GAATTCCTGGACTCAAGCAGTTAACCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAG T C MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE38233;GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,32596459 RNA-Seq:(High) rs1280900594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8478819,Human_RBP_ID_13383810,Human_RBP_ID_23309321 RMVar_hsa_circ_86392,RMVar_hsa_circ_191099 23591 RMVar_ID_23591 Human_SNP_ID_655471962 A-to-I Human chr19 - 1590430 1590430 1590430 TAGAGATGGGGTTTTGCTGTGTTGCCTAGACTAGACTGGTCTCGAATTCCTGGACTCAAGCAGTT TAGAGATGGGGTTTTGCTGTGTTGCCTAGACTGGACTGGTCTCGAATTCCTGGACTCAAGCAGTT T C MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE38233;GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,32596459 RNA-Seq:(High) rs903782774 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_514924,Human_RBP_ID_1292332,Human_RBP_ID_3564006,Human_RBP_ID_6724496,Human_RBP_ID_13383810,Human_RBP_ID_26471596 RMVar_hsa_circ_86392,RMVar_hsa_circ_191099 23592 RMVar_ID_23592 Human_SNP_ID_655471970 A-to-I Human chr19 - 1590461 1590461 1590461 GGCACGTGCCACCATACCTGGCTTATTTTTATAGAGATGGGGTTTTGCTGTGTTGCCTAGACTAG GGCACGTGCCACCATACCTGGCTTATTTTTATGGAGATGGGGTTTTGCTGTGTTGCCTAGACTAG T C MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs956728726 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6724496,Human_RBP_ID_9084823,Human_RBP_ID_13383810,Human_RBP_ID_17916348,Human_RBP_ID_27675011 RMVar_hsa_circ_86392,RMVar_hsa_circ_191099 23593 RMVar_ID_23593 Human_SNP_ID_655471980 A-to-I Human chr19 - 1590499 1590499 1590499 ACCCTCTCAGCTCAGCCTCCCAAGTAGTGGGAATTACAGGCACGTGCCACCATACCTGGCTTATT ACCCTCTCAGCTCAGCCTCCCAAGTAGTGGGAGTTACAGGCACGTGCCACCATACCTGGCTTATT T C MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs980104298 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86392,RMVar_hsa_circ_191099 23594 RMVar_ID_23594 Human_SNP_ID_655471981 A-to-I Human chr19 - 1590506 1590503 1590506 TCAGGCGACCCTCTCAGCTCAGCCTCCCAAGTAGTGGGAATTACAGGCACGTGCCACCATACCTG TCAGGCGACCCTCTCAGCTCAGCCTCCCAAGT___GGGAATTACAGGCACGTGCCACCATACCTG CACT C MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs535008726 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_86392,RMVar_hsa_circ_191099 23595 RMVar_ID_23595 Human_SNP_ID_655471983 A-to-I Human chr19 - 1590509 1590509 1590509 GGCTCAGGCGACCCTCTCAGCTCAGCCTCCCAAGTAGTGGGAATTACAGGCACGTGCCACCATAC GGCTCAGGCGACCCTCTCAGCTCAGCCTCCCAGGTAGTGGGAATTACAGGCACGTGCCACCATAC T C MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1313251868 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86392,RMVar_hsa_circ_191099 23596 RMVar_ID_23596 Human_SNP_ID_655471994 A-to-I Human chr19 - 1590542 1590541 1590543 TACAATCACGGCTTACGCATTCTTGACCTCCCAGGCTCAGGCGACCCTCTCAGCTCAGCCTCCCA TACAATCACGGCTTACGCATTCTTGACCTCC__GGCTCAGGCGACCCTCTCAGCTCAGCCTCCCA CTG C MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE38233;GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,32596459 RNA-Seq:(High) rs750169109 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_6724499,Human_RBP_ID_13383819 RMVar_hsa_circ_86392,RMVar_hsa_circ_191099 23597 RMVar_ID_23597 Human_SNP_ID_655472003 A-to-I Human chr19 - 1590567 1590567 1590567 TCTCACCCAGGCTGGAGTGCAGTGGTACAATCACGGCTTACGCATTCTTGACCTCCCAGGCTCAG TCTCACCCAGGCTGGAGTGCAGTGGTACAATCGCGGCTTACGCATTCTTGACCTCCCAGGCTCAG T C MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1203014614 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_514925,Human_RBP_ID_2557999,Human_RBP_ID_4507297,Human_RBP_ID_13383819,Human_RBP_ID_26984430 RMVar_hsa_circ_86392,RMVar_hsa_circ_191099 23598 RMVar_ID_23598 Human_SNP_ID_655472004 A-to-I Human chr19 - 1590573 1590573 1590573 ACAGGGTCTCACCCAGGCTGGAGTGCAGTGGTACAATCACGGCTTACGCATTCTTGACCTCCCAG ACAGGGTCTCACCCAGGCTGGAGTGCAGTGGTGCAATCACGGCTTACGCATTCTTGACCTCCCAG T C MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE100210;GSE107867 HepG2 cell line;ASD brains,cerebellum - 29129909,30559470 RNA-Seq:(High) rs950741000 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_239156,Human_RBP_ID_514925,Human_RBP_ID_2557999,Human_RBP_ID_13383821,Human_RBP_ID_26465356,Human_RBP_ID_26984430 RMVar_hsa_circ_86392,RMVar_hsa_circ_191099 23599 RMVar_ID_23599 Human_SNP_ID_655472011 A-to-I Human chr19 - 1590603 1590601 1590603 AAGCTACCTTTTTTGTTTTTTTTCTTTGAGACAGGGTCTCACCCAGGCTGGAGTGCAGTGGTACA AAGCTACCTTTTTTGTTTTTTTTCTTTGAGAC__GGTCTCACCCAGGCTGGAGTGCAGTGGTACA CCT C MBD3,AC005943.1 Ensembl:ENSG00000071655,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs556837177 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_514925,Human_RBP_ID_2558000,Human_RBP_ID_6724501,Human_RBP_ID_13545429,Human_RBP_ID_17916350 RMVar_hsa_circ_86392,RMVar_hsa_circ_191099 23600 RMVar_ID_23600 Human_SNP_ID_655473982 A-to-I Human chr19 - 1595568 1595568 1595568 CCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCACACCCGGCCTTGATGACATTTT CCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCACACCCGGCCTTGATGACATTTT T C AC005943.1 Ensembl:ENSG00000267059 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879401904 Functional Loss SNV dbSNP153 33..33 33 - - - 23601 RMVar_ID_23601 Human_SNP_ID_655474314 A-to-I Human chr19 - 1596727 1596727 1596727 AGCCTATTTATTTATTTATTTTTGGAGATGGAATCTTACTGTGTCACCCAGGTTGGAGTGCAGTG AGCCTATTTATTTATTTATTTTTGGAGATGGAGTCTTACTGTGTCACCCAGGTTGGAGTGCAGTG T C AC005943.1 Ensembl:ENSG00000267059 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs936555740 Functional Loss SNV dbSNP153 33..33 33 - - - 23602 RMVar_ID_23602 Human_SNP_ID_655474315 A-to-I Human chr19 - 1596727 1596727 1596727 AGCCTATTTATTTATTTATTTTTGGAGATGGAATCTTACTGTGTCACCCAGGTTGGAGTGCAGTG AGCCTATTTATTTATTTATTTTTGGAGATGGACTCTTACTGTGTCACCCAGGTTGGAGTGCAGTG T G AC005943.1 Ensembl:ENSG00000267059 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs936555740 Functional Loss SNV dbSNP153 33..33 33 - - - 23603 RMVar_ID_23603 Human_SNP_ID_655474789 A-to-I Human chr19 - 1598481 1598481 1598481 GGAGCGCAATGACGCGATCTTGGCGCACTGCAACCTCCACCTCCCGGGTTCAAGCGATTCTCCTG GGAGCGCAATGACGCGATCTTGGCGCACTGCACCCTCCACCTCCCGGGTTCAAGCGATTCTCCTG T G UQCR11,AC005943.1 Ensembl:ENSG00000127540,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1223248061 Functional Loss SNV dbSNP153 33..33 33 - - - 23604 RMVar_ID_23604 Human_SNP_ID_655474791 A-to-I Human chr19 - 1598487 1598487 1598487 CAGGCTGGAGCGCAATGACGCGATCTTGGCGCACTGCAACCTCCACCTCCCGGGTTCAAGCGATT CAGGCTGGAGCGCAATGACGCGATCTTGGCGCGCTGCAACCTCCACCTCCCGGGTTCAAGCGATT T C UQCR11,AC005943.1 Ensembl:ENSG00000127540,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1371321960 Functional Loss SNV dbSNP153 33..33 33 - - - 23605 RMVar_ID_23605 Human_SNP_ID_655475330 A-to-I Human chr19 - 1600036 1600036 1600036 CTCTCACAGCACGTGCCGTGGTGGGCAAGAGCATGAGCTTGGAACCGGAGGCCTCGATCCTCGCC CTCTCACAGCACGTGCCGTGGTGGGCAAGAGCTTGAGCTTGGAACCGGAGGCCTCGATCCTCGCC T A UQCR11,AC005943.1 Ensembl:ENSG00000127540,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs887390 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17568225 RMVar_hsa_circ_124367,RMVar_hsa_circ_191103 23606 RMVar_ID_23606 Human_SNP_ID_655475331 A-to-I Human chr19 - 1600036 1600036 1600036 CTCTCACAGCACGTGCCGTGGTGGGCAAGAGCATGAGCTTGGAACCGGAGGCCTCGATCCTCGCC CTCTCACAGCACGTGCCGTGGTGGGCAAGAGCGTGAGCTTGGAACCGGAGGCCTCGATCCTCGCC T C UQCR11,AC005943.1 Ensembl:ENSG00000127540,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs887390 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17568225 RMVar_hsa_circ_124367,RMVar_hsa_circ_191103 23607 RMVar_ID_23607 Human_SNP_ID_655475332 A-to-I Human chr19 - 1600036 1600036 1600036 CTCTCACAGCACGTGCCGTGGTGGGCAAGAGCATGAGCTTGGAACCGGAGGCCTCGATCCTCGCC CTCTCACAGCACGTGCCGTGGTGGGCAAGAGCCTGAGCTTGGAACCGGAGGCCTCGATCCTCGCC T G UQCR11,AC005943.1 Ensembl:ENSG00000127540,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs887390 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17568225 RMVar_hsa_circ_124367,RMVar_hsa_circ_191103 23608 RMVar_ID_23608 Human_SNP_ID_655475940 A-to-I Human chr19 - 1601945 1601945 1601945 GTTGGCCAGGCTGGTCTAGAATTCCTGACCTCAGGTGATCCACCCGCCTCGGCCTCCGGAAGTGC GTTGGCCAGGCTGGTCTAGAATTCCTGACCTCGGGTGATCCACCCGCCTCGGCCTCCGGAAGTGC T C UQCR11,AC005943.1 Ensembl:ENSG00000127540,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1175580365 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124367,RMVar_hsa_circ_191103 23609 RMVar_ID_23609 Human_SNP_ID_655475983 A-to-I Human chr19 - 1602118 1602118 1602118 TCTCACTGTCGCCCAAGCTAGAGTGCAGTGGCACGATCTCGGCTCACTGCAACCTCGACCTACAG TCTCACTGTCGCCCAAGCTAGAGTGCAGTGGCGCGATCTCGGCTCACTGCAACCTCGACCTACAG T C UQCR11,AC005943.1 Ensembl:ENSG00000127540,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1383088344 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1933481 RMVar_hsa_circ_124367,RMVar_hsa_circ_191103 23610 RMVar_ID_23610 Human_SNP_ID_655476139 A-to-I Human chr19 - 1602589 1602589 1602589 AAATTAGTCGGGCGCGGTAGTGGACACCTGTAATCCCAGCTTCATGGGAGGCTGAGACAAGAGAA AAATTAGTCGGGCGCGGTAGTGGACACCTGTACTCCCAGCTTCATGGGAGGCTGAGACAAGAGAA T G UQCR11,AC005943.1 Ensembl:ENSG00000127540,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1442770086 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124367,RMVar_hsa_circ_191103 23611 RMVar_ID_23611 Human_SNP_ID_655476152 A-to-I Human chr19 - 1602616 1602616 1602616 GAAACCCTGTCTCTACTAAAAATACAAAAATTAGTCGGGCGCGGTAGTGGACACCTGTAATCCCA GAAACCCTGTCTCTACTAAAAATACAAAAATTGGTCGGGCGCGGTAGTGGACACCTGTAATCCCA T C UQCR11,AC005943.1 Ensembl:ENSG00000127540,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs577537364 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124367,RMVar_hsa_circ_191103 23612 RMVar_ID_23612 Human_SNP_ID_655476647 A-to-I Human chr19 - 1604410 1604410 1604410 GCCTGGGAGTTCAAGACCATCCTGGACAACACAATGAAACCCCATCTCTACAAAACAAAAAATTA GCCTGGGAGTTCAAGACCATCCTGGACAACACTATGAAACCCCATCTCTACAAAACAAAAAATTA T A UQCR11,AC005943.1 Ensembl:ENSG00000127540,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1173293320 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18532284,Human_RBP_ID_22230675 RMVar_hsa_circ_124367,RMVar_hsa_circ_191103 23613 RMVar_ID_23613 Human_SNP_ID_655476759 A-to-I Human chr19 - 1604775 1604774 1604775 CCTGTGATCCCAGCGCTTTGTGAGGCCGAGGCAGGTGGATCACCTGAGGTCAGGAGTTCGAGACC CCTGTGATCCCAGCGCTTTGTGAGGCCGAGGC_GGTGGATCACCTGAGGTCAGGAGTTCGAGACC CT C UQCR11,AC005943.1 Ensembl:ENSG00000127540,Ensembl:ENSG00000267059 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1342787325 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_124367,RMVar_hsa_circ_191103 23614 RMVar_ID_23614 Human_SNP_ID_655522062 A-to-I Human chr19 - 1727511 1727511 1727511 ATTATTATTTTTTAGGCTGGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAG ATTATTATTTTTTAGGCTGGGCGCAGTGGCTCGCGCCTGTAATCCCAGCACTTTGGGAGGCTGAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1282986398 Functional Loss SNV dbSNP153 33..33 33 - - - 23615 RMVar_ID_23615 Human_SNP_ID_655522067 A-to-I Human chr19 - 1727519 1727519 1727519 TTTAAATTATTATTATTTTTTAGGCTGGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGG TTTAAATTATTATTATTTTTTAGGCTGGGCGCCGTGGCTCACGCCTGTAATCCCAGCACTTTGGG T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017420540 Functional Loss SNV dbSNP153 33..33 33 - - - 23616 RMVar_ID_23616 Human_SNP_ID_655546515 A-to-I Human chr19 - 1798971 1798971 1798971 ACCCAGCTTATTTTTGTATTTTTTGTCAAGACAGGGAATCCCTATGTTGCCCAGGCTGGTCTTGA ACCCAGCTTATTTTTGTATTTTTTGTCAAGACGGGGAATCCCTATGTTGCCCAGGCTGGTCTTGA T C ATP8B3 Ensembl:ENSG00000130270 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1227058551 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_515933,Human_RBP_ID_13392951 RMVar_hsa_circ_84956,RMVar_hsa_circ_101953,RMVar_hsa_circ_191117,RMVar_hsa_circ_191118 23617 RMVar_ID_23617 Human_SNP_ID_655555959 A-to-I Human chr19 - 1825134 1825134 1825134 CACCACACCAGGCTAATTTTTGTATCTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGACTGG CACCACACCAGGCTAATTTTTGTATCTTTAGTGGAGACGGGGTTTCACCATGTTGGCCAGACTGG T C REXO1 Ensembl:ENSG00000079313 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1411239880 Functional Loss SNV dbSNP153 33..33 33 - - - 23618 RMVar_ID_23618 Human_SNP_ID_655555960 A-to-I Human chr19 - 1825152 1825152 1825152 GGGATTACAGGTGCCCACCACCACACCAGGCTAATTTTTGTATCTTTAGTAGAGACGGGGTTTCA GGGATTACAGGTGCCCACCACCACACCAGGCTGATTTTTGTATCTTTAGTAGAGACGGGGTTTCA T C REXO1 Ensembl:ENSG00000079313 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1397682067 Functional Loss SNV dbSNP153 33..33 33 - - - 23619 RMVar_ID_23619 Human_SNP_ID_655556152 A-to-I Human chr19 - 1825591 1825591 1825591 GGTGCCTGTAATACCAGCTACTAGAGAGGCTGAGGCAGGAGAATCGCTTGAACTCAGGAGGCAGA GGTGCCTGTAATACCAGCTACTAGAGAGGCTGGGGCAGGAGAATCGCTTGAACTCAGGAGGCAGA T C REXO1 Ensembl:ENSG00000079313 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs951119769 Functional Loss SNV dbSNP153 33..33 33 - - - 23620 RMVar_ID_23620 Human_SNP_ID_655556157 A-to-I Human chr19 - 1825601 1825601 1825601 CATGGTGATGGGTGCCTGTAATACCAGCTACTAGAGAGGCTGAGGCAGGAGAATCGCTTGAACTC CATGGTGATGGGTGCCTGTAATACCAGCTACTGGAGAGGCTGAGGCAGGAGAATCGCTTGAACTC T C REXO1 Ensembl:ENSG00000079313 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1358000411 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25389067 23621 RMVar_ID_23621 Human_SNP_ID_655556187 A-to-I Human chr19 - 1825727 1825727 1825727 TCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGTGGATCACCTGAGGCCAGGAGTTCG TCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGTGGATCACCTGAGGCCAGGAGTTCG T C REXO1 Ensembl:ENSG00000079313 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs542513198 Functional Loss SNV dbSNP153 33..33 33 - - - 23622 RMVar_ID_23622 Human_SNP_ID_655558025 A-to-I Human chr19 - 1829307 1829307 1829307 TTGAACTCGGGAGATAGAGGCTGCGGTGAGCCAAGATCGCACCACTATACTCCAGCTTGGGCAGC TTGAACTCGGGAGATAGAGGCTGCGGTGAGCCGAGATCGCACCACTATACTCCAGCTTGGGCAGC T C REXO1 Ensembl:ENSG00000079313 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1463126158 Functional Loss SNV dbSNP153 33..33 33 - - - 23623 RMVar_ID_23623 Human_SNP_ID_655558363 A-to-I Human chr19 - 1830393 1830393 1830393 GTGATTCTCCCACTTTAGCCTCCCACATAGCTAGGAGCACAGGTGTGCATCACCATGCTCAGCTT GTGATTCTCCCACTTTAGCCTCCCACATAGCTGGGAGCACAGGTGTGCATCACCATGCTCAGCTT T C REXO1 Ensembl:ENSG00000079313 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs999227491 Functional Loss SNV dbSNP153 33..33 33 - - - 23624 RMVar_ID_23624 Human_SNP_ID_655559642 A-to-I Human chr19 - 1834645 1834645 1834645 GGGAGGCCGAGGCGAGAAGACCGCTTGAGCTTAGAAGTTTGAGACCAGCCTGGGCAATTACAGCG GGGAGGCCGAGGCGAGAAGACCGCTTGAGCTTCGAAGTTTGAGACCAGCCTGGGCAATTACAGCG T G REXO1 Ensembl:ENSG00000079313 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1447763591 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13393620 23625 RMVar_ID_23625 Human_SNP_ID_655559646 A-to-I Human chr19 - 1834660 1834660 1834660 GACAAGCAGTGCTTTGGGAGGCCGAGGCGAGAAGACCGCTTGAGCTTAGAAGTTTGAGACCAGCC GACAAGCAGTGCTTTGGGAGGCCGAGGCGAGATGACCGCTTGAGCTTAGAAGTTTGAGACCAGCC T A REXO1 Ensembl:ENSG00000079313 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs996698784 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6726468,Human_RBP_ID_13393620 23626 RMVar_ID_23626 Human_SNP_ID_655584219 A-to-I Human chr19 + 1906757 1906757 1906757 TGGTCCCGGCTACTCCCAAAGGAGGCTGAGGCAGGAAAATGGTGTGAACTCAGGAGGCAGAGCTT TGGTCCCGGCTACTCCCAAAGGAGGCTGAGGCGGGAAAATGGTGTGAACTCAGGAGGCAGAGCTT A G SCAMP4,ADAT3 Ensembl:ENSG00000227500,Ensembl:ENSG00000213638 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991957158 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_138879,Human_RBP_ID_8480166 RMVar_hsa_circ_95677,RMVar_hsa_circ_191124 23627 RMVar_ID_23627 Human_SNP_ID_655585775 A-to-I Human chr19 + 1910907 1910907 1910907 TTTTTGTTGTTTTTTGACAGTCTCGCGCTGTTACCAGGCTGGAGTGCAGTGGCGCGATCTCGGCT TTTTTGTTGTTTTTTGACAGTCTCGCGCTGTTTCCAGGCTGGAGTGCAGTGGCGCGATCTCGGCT A T SCAMP4,ADAT3 Ensembl:ENSG00000227500,Ensembl:ENSG00000213638 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1298897774 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95677,RMVar_hsa_circ_191124 23628 RMVar_ID_23628 Human_SNP_ID_655585916 A-to-I Human chr19 + 1911357 1911357 1911357 CCACGCCCAGCTAATTTTTTGATATTTAGTAGAAATGGGGTGTTGTTATGTTGCCTAGGCTGGTC CCACGCCCAGCTAATTTTTTGATATTTAGTAGGAATGGGGTGTTGTTATGTTGCCTAGGCTGGTC A G SCAMP4,ADAT3 Ensembl:ENSG00000227500,Ensembl:ENSG00000213638 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1423573244 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13398489,Human_RBP_ID_22967831 RMVar_hsa_circ_95677,RMVar_hsa_circ_191124 23629 RMVar_ID_23629 Human_SNP_ID_655587870 A-to-I Human chr19 + 1915825 1915825 1915825 AAAATTAGCTGGGCGTGGTGGCGGGTGCCTGTAGTCCCAGCTACTCGAGAGGCTGAGGCAGGAGA AAAATTAGCTGGGCGTGGTGGCGGGTGCCTGTTGTCCCAGCTACTCGAGAGGCTGAGGCAGGAGA A T SCAMP4 Ensembl:ENSG00000227500 Protein coding intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1364929340 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95677,RMVar_hsa_circ_191124 23630 RMVar_ID_23630 Human_SNP_ID_655588107 A-to-I Human chr19 + 1916484 1916484 1916484 TATTTGTTGTGTTCTTTGTTTTGTTTTGAGACAGGGTCTGGGTCTCTCCCAGGCTGGAGTGCAGT TATTTGTTGTGTTCTTTGTTTTGTTTTGAGACGGGGTCTGGGTCTCTCCCAGGCTGGAGTGCAGT A G SCAMP4 Ensembl:ENSG00000227500 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1163919165 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3564782 RMVar_hsa_circ_95677,RMVar_hsa_circ_191124 23631 RMVar_ID_23631 Human_SNP_ID_655588322 A-to-I Human chr19 + 1917185 1917185 1917185 AAAATTAGCCGGGTGTGGTGGTGGGCGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGAAGA AAAATTAGCCGGGTGTGGTGGTGGGCGCCTGTGATCCCAGCTACTTGGGAGGCTGAGGCAGAAGA A G SCAMP4 Ensembl:ENSG00000227500 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229,31158229 RNA-Seq:(High) rs1426296101 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95677,RMVar_hsa_circ_191124 23632 RMVar_ID_23632 Human_SNP_ID_655599518 A-to-I Human chr19 + 1946433 1946433 1946433 CCTGCCTCAGCTTCCCGAGTAGCTGGGACTACAGGCGACCGCCACCACGCCTGGCTAGTTTTTTG CCTGCCTCAGCTTCCCGAGTAGCTGGGACTACGGGCGACCGCCACCACGCCTGGCTAGTTTTTTG A G CSNK1G2 Ensembl:ENSG00000133275 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1051105869 Functional Loss SNV dbSNP153 33..33 33 - - - 23633 RMVar_ID_23633 Human_SNP_ID_655610581 A-to-I Human chr19 + 1975764 1975764 1975764 GAGCTCTAAAACTTCGAAATCTGACCAGGCACAGTGGCTCACGCCTGTAATCCCAACACTTTGGG GAGCTCTAAAACTTCGAAATCTGACCAGGCACGGTGGCTCACGCCTGTAATCCCAACACTTTGGG A G CSNK1G2 Ensembl:ENSG00000133275 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs549521259 Functional Loss SNV dbSNP153 33..33 33 - - - 23634 RMVar_ID_23634 Human_SNP_ID_655610647 A-to-I Human chr19 + 1975928 1975928 1975928 TTGATGGTGCCTGCCTGTAATTCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACCCA TTGATGGTGCCTGCCTGTAATTCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCA A G CSNK1G2 Ensembl:ENSG00000133275 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs967158927 Functional Loss SNV dbSNP153 33..33 33 - - - 23635 RMVar_ID_23635 Human_SNP_ID_655610944 A-to-I Human chr19 + 1976857 1976857 1976857 CACCTCCCGGGTTCAGGCAATTCTCCTGCCTCAGCCTCCCTGGTAGCTGGGATTACAGGCATGCA CACCTCCCGGGTTCAGGCAATTCTCCTGCCTCGGCCTCCCTGGTAGCTGGGATTACAGGCATGCA A G CSNK1G2 Ensembl:ENSG00000133275 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs894417056 Functional Loss SNV dbSNP153 33..33 33 - - - 23636 RMVar_ID_23636 Human_SNP_ID_655611235 A-to-I Human chr19 + 1977716 1977716 1977716 CAAAGGCTGCAGTGAACTGCGATCTCGCCACTACACTCCAGACTGGGCAACAGAGCGACACCGTC CAAAGGCTGCAGTGAACTGCGATCTCGCCACTGCACTCCAGACTGGGCAACAGAGCGACACCGTC A G CSNK1G2 Ensembl:ENSG00000133275 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1040886984 Functional Loss SNV dbSNP153 33..33 33 - - - 23637 RMVar_ID_23637 Human_SNP_ID_655617275 A-to-I Human chr19 - 1992001 1992001 1992001 CAGCTCACTGCAACCTCCGCCTCCAGCGTTCAAGCGATTCTCCTGCCTCAGCCTCCACAGTAGCT CAGCTCACTGCAACCTCCGCCTCCAGCGTTCAGGCGATTCTCCTGCCTCAGCCTCCACAGTAGCT T C BTBD2 Ensembl:ENSG00000133243 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1175143684 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1934468 RMVar_hsa_circ_18236,RMVar_hsa_circ_39273,RMVar_hsa_circ_39383,RMVar_hsa_circ_288823,RMVar_hsa_circ_348230 23638 RMVar_ID_23638 Human_SNP_ID_655617345 A-to-I Human chr19 - 1992200 1992200 1992200 GAATCTCAACTACTTGGGGGACCAAAGCAGGAAGATTGCCTGAGCCCGGGAGGTTGAGGCTGCAG GAATCTCAACTACTTGGGGGACCAAAGCAGGATGATTGCCTGAGCCCGGGAGGTTGAGGCTGCAG T A BTBD2 Ensembl:ENSG00000133243 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs117911070 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18236,RMVar_hsa_circ_39273,RMVar_hsa_circ_39383,RMVar_hsa_circ_288823,RMVar_hsa_circ_348230 23639 RMVar_ID_23639 Human_SNP_ID_655617346 A-to-I Human chr19 - 1992200 1992200 1992200 GAATCTCAACTACTTGGGGGACCAAAGCAGGAAGATTGCCTGAGCCCGGGAGGTTGAGGCTGCAG GAATCTCAACTACTTGGGGGACCAAAGCAGGAGGATTGCCTGAGCCCGGGAGGTTGAGGCTGCAG T C BTBD2 Ensembl:ENSG00000133243 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs117911070 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18236,RMVar_hsa_circ_39273,RMVar_hsa_circ_39383,RMVar_hsa_circ_288823,RMVar_hsa_circ_348230 23640 RMVar_ID_23640 Human_SNP_ID_655620826 A-to-I Human chr19 - 2001440 2001440 2001440 TAGCCCAGGGTGCAGTGCAGTGGTACGATCTCAGCTCACTGCGACCTCCGCCTCCAGGGTTCAAG TAGCCCAGGGTGCAGTGCAGTGGTACGATCTCCGCTCACTGCGACCTCCGCCTCCAGGGTTCAAG T G BTBD2 Ensembl:ENSG00000133243 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1036906473 Functional Loss SNV dbSNP153 33..33 33 - - - 23641 RMVar_ID_23641 Human_SNP_ID_655621010 A-to-I Human chr19 - 2002013 2002013 2002013 ATCTCTTCCAGGCGTGGGGGCTCACACCTGTAATCCCAGCACTTTGGGAGACGGAGGCGGGCGGA ATCTCTTCCAGGCGTGGGGGCTCACACCTGTAGTCCCAGCACTTTGGGAGACGGAGGCGGGCGGA T C BTBD2 Ensembl:ENSG00000133243 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1442439771 Functional Loss SNV dbSNP153 33..33 33 - - - 23642 RMVar_ID_23642 Human_SNP_ID_655621085 A-to-I Human chr19 - 2002280 2002279 2002281 GCCCAGGGGTTTGAGACCAGCCTGGGCAACATAGCGAGACCCCGTCTGTACAAAACATTTAACAG GCCCAGGGGTTTGAGACCAGCCTGGGCAACA__GCGAGACCCCGTCTGTACAAAACATTTAACAG CTA C BTBD2 Ensembl:ENSG00000133243 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1329636306 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_140197 23643 RMVar_ID_23643 Human_SNP_ID_655621197 A-to-I Human chr19 - 2002611 2002611 2002611 CCTCGGCCTCCTAAAGTGCTGGGATTACAGGCATGAGCCCCTGTGCCCGGCGGCATCCTACAATT CCTCGGCCTCCTAAAGTGCTGGGATTACAGGCGTGAGCCCCTGTGCCCGGCGGCATCCTACAATT T C BTBD2,AC004678.2 Ensembl:ENSG00000133243,Ensembl:ENSG00000279653 Protein coding,Other intron,exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1045170015 Functional Loss SNV dbSNP153 33..33 33 - - - 23644 RMVar_ID_23644 Human_SNP_ID_655622344 A-to-I Human chr19 - 2006082 2006082 2006082 AAAATTAAATTTTTTTTTTTTTTTTTAGAGACAGGGTCTCACTCTGTCACCCACACTGGAGTTCA AAAATTAAATTTTTTTTTTTTTTTTTAGAGACTGGGTCTCACTCTGTCACCCACACTGGAGTTCA T A BTBD2 Ensembl:ENSG00000133243 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1476477120 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6801709,Human_RBP_ID_13406625,Human_RBP_ID_17567471 23645 RMVar_ID_23645 Human_SNP_ID_655622591 A-to-I Human chr19 - 2006826 2006826 2006826 AAATTAGCTGGGCATGGTGGTGAGCACCTGTAATCCCAGCTACGTAGGAGGCTGAGGCAGGAGAA AAATTAGCTGGGCATGGTGGTGAGCACCTGTAGTCCCAGCTACGTAGGAGGCTGAGGCAGGAGAA T C BTBD2 Ensembl:ENSG00000133243 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1391095176 Functional Loss SNV dbSNP153 33..33 33 - - - 23646 RMVar_ID_23646 Human_SNP_ID_655645577 A-to-I Human chr19 - 2074182 2074182 2074182 TCAAGTGATTCCCCTCCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCATGTGCCACCATACCTG TCAAGTGATTCCCCTCCCTCAGCCTCCTGAGTCGCTGGGACTACAGGCATGTGCCACCATACCTG T G MOB3A Ensembl:ENSG00000172081 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1016835321 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116122,RMVar_hsa_circ_127597,RMVar_hsa_circ_118892,RMVar_hsa_circ_191139,RMVar_hsa_circ_191141,RMVar_hsa_circ_191140 23647 RMVar_ID_23647 Human_SNP_ID_655645753 A-to-I Human chr19 - 2074855 2074855 2074855 AAATTAGCTGGGCATGGTGGCACGCGCCTGTAATTCCAGCTACTCGGGAGGCTGAGGCAGAAGAA AAATTAGCTGGGCATGGTGGCACGCGCCTGTAGTTCCAGCTACTCGGGAGGCTGAGGCAGAAGAA T C MOB3A Ensembl:ENSG00000172081 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1256908191 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116122,RMVar_hsa_circ_127597,RMVar_hsa_circ_118892,RMVar_hsa_circ_191139,RMVar_hsa_circ_191141,RMVar_hsa_circ_191140 23648 RMVar_ID_23648 Human_SNP_ID_655645898 A-to-I Human chr19 - 2075334 2075334 2075334 CACCACTCTCTTACAACTTTAAAAAATGGTTAAAAATGGACGGACGAGGTGGCTCCCACCAGTAA CACCACTCTCTTACAACTTTAAAAAATGGTTACAAATGGACGGACGAGGTGGCTCCCACCAGTAA T G MOB3A Ensembl:ENSG00000172081 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1237105813 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116122,RMVar_hsa_circ_127597,RMVar_hsa_circ_118892,RMVar_hsa_circ_191139,RMVar_hsa_circ_191141,RMVar_hsa_circ_191140 23649 RMVar_ID_23649 Human_SNP_ID_655646817 A-to-I Human chr19 - 2077952 2077952 2077952 AGCAAGATCCCATCTCTACAAAAAATTTTAAAAATTAGCCAGGCATGGTGGCACACGCCTTTGGT AGCAAGATCCCATCTCTACAAAAAATTTTAAACATTAGCCAGGCATGGTGGCACACGCCTTTGGT T G MOB3A Ensembl:ENSG00000172081 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1029879157 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116122,RMVar_hsa_circ_127597,RMVar_hsa_circ_118892,RMVar_hsa_circ_191139,RMVar_hsa_circ_191141,RMVar_hsa_circ_191140,RMVar_hsa_circ_277521,RMVar_hsa_circ_191142 23650 RMVar_ID_23650 Human_SNP_ID_655647738 A-to-I Human chr19 - 2080600 2080600 2080600 GGCCAAGGTGGGCGGATCAGATGAGGTCAGGAATTCGAGACCAGCCTGGCCAGCATGGTAAAACC GGCCAAGGTGGGCGGATCAGATGAGGTCAGGAGTTCGAGACCAGCCTGGCCAGCATGGTAAAACC T C MOB3A Ensembl:ENSG00000172081 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs534796710 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23788124 RMVar_hsa_circ_116122,RMVar_hsa_circ_118892,RMVar_hsa_circ_191141,RMVar_hsa_circ_191140,RMVar_hsa_circ_337015,RMVar_hsa_circ_191144 23651 RMVar_ID_23651 Human_SNP_ID_655648150 A-to-I Human chr19 - 2081736 2081736 2081736 GGAATTTCAGGCATGCACCATCACGCCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCA GGAATTTCAGGCATGCACCATCACGCCTGGCTGATTTTTGTATTTTTAGTAGAGACAGGGTTTCA T C MOB3A Ensembl:ENSG00000172081 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs891271966 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116122,RMVar_hsa_circ_118892,RMVar_hsa_circ_191141,RMVar_hsa_circ_191140,RMVar_hsa_circ_337015,RMVar_hsa_circ_191144 23652 RMVar_ID_23652 Human_SNP_ID_655648505 A-to-I Human chr19 - 2083046 2083045 2083047 GTCCAGGAGTTCAAGACCAGCCTAGGCAACATAGTGAGCTCCCGTCTCTACAAAAAATACAACAA GTCCAGGAGTTCAAGACCAGCCTAGGCAACA__GTGAGCTCCCGTCTCTACAAAAAATACAACAA CTA C MOB3A Ensembl:ENSG00000172081 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1307061161 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_116122,RMVar_hsa_circ_118892,RMVar_hsa_circ_191141,RMVar_hsa_circ_191140,RMVar_hsa_circ_337015,RMVar_hsa_circ_191144 23653 RMVar_ID_23653 Human_SNP_ID_655650750 A-to-I Human chr19 - 2090775 2090775 2090775 GCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCAGTAGGCGGAGGTT GCTGTAATCCCAGCTACTCGGGAGGCTGAGGCCGGAGAATGGCGTGAACCCAGTAGGCGGAGGTT T G MOB3A Ensembl:ENSG00000172081 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1380480783 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118892,RMVar_hsa_circ_191141 23654 RMVar_ID_23654 Human_SNP_ID_655650765 A-to-I Human chr19 - 2090846 2090846 2090846 CATCCTGACTAACACGGTGAAACCCCGTCTCTACTAAAAATTCAAAAATTAGCTGAGCACGGTTG CATCCTGACTAACACGGTGAAACCCCGTCTCTGCTAAAAATTCAAAAATTAGCTGAGCACGGTTG T C MOB3A Ensembl:ENSG00000172081 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1049388607 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118892,RMVar_hsa_circ_191141 23655 RMVar_ID_23655 Human_SNP_ID_655663548 A-to-I Human chr19 - 2124818 2124818 2124818 CTCCTGCCTCAGCCTCCAGAGTAGCTGGGGTTACAGACATGCTCCACCACTCCCGCTTATTTTTG CTCCTGCCTCAGCCTCCAGAGTAGCTGGGGTTGCAGACATGCTCCACCACTCCCGCTTATTTTTG T C AP3D1 Ensembl:ENSG00000065000 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs994597176 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_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_95127,RMVar_hsa_circ_111584,RMVar_hsa_circ_191166,RMVar_hsa_circ_127420,RMVar_hsa_circ_191167,RMVar_hsa_circ_191168,RMVar_hsa_circ_78057,RMVar_hsa_circ_191169 23656 RMVar_ID_23656 Human_SNP_ID_655663752 A-to-I Human chr19 - 2125392 2125392 2125392 AGAATTGCTTGAACCAGGGAGGCAGAGGTTGCAGTGAGCCAAGATTGTGCCGTTGCACTCCAGCC AGAATTGCTTGAACCAGGGAGGCAGAGGTTGCGGTGAGCCAAGATTGTGCCGTTGCACTCCAGCC T C AP3D1 Ensembl:ENSG00000065000 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1414808006 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_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_95127,RMVar_hsa_circ_111584,RMVar_hsa_circ_191166,RMVar_hsa_circ_127420,RMVar_hsa_circ_191167,RMVar_hsa_circ_191168,RMVar_hsa_circ_78057,RMVar_hsa_circ_191169 23657 RMVar_ID_23657 Human_SNP_ID_655663759 A-to-I Human chr19 - 2125444 2125444 2125444 GGGCTTGGTGTCGGGCGCCTGTAATCCCGACTACTTGGGAGGCTGAAGCAGGAGAATTGCTTGAA GGGCTTGGTGTCGGGCGCCTGTAATCCCGACTTCTTGGGAGGCTGAAGCAGGAGAATTGCTTGAA T A AP3D1 Ensembl:ENSG00000065000 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs998922427 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_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_95127,RMVar_hsa_circ_111584,RMVar_hsa_circ_191166,RMVar_hsa_circ_127420,RMVar_hsa_circ_191167,RMVar_hsa_circ_191168,RMVar_hsa_circ_78057,RMVar_hsa_circ_191169 23658 RMVar_ID_23658 Human_SNP_ID_655663764 A-to-I Human chr19 - 2125453 2125453 2125453 AAATTAGCAGGGCTTGGTGTCGGGCGCCTGTAATCCCGACTACTTGGGAGGCTGAAGCAGGAGAA AAATTAGCAGGGCTTGGTGTCGGGCGCCTGTATTCCCGACTACTTGGGAGGCTGAAGCAGGAGAA T A AP3D1 Ensembl:ENSG00000065000 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1330552489 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_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_95127,RMVar_hsa_circ_111584,RMVar_hsa_circ_191166,RMVar_hsa_circ_127420,RMVar_hsa_circ_191167,RMVar_hsa_circ_191168,RMVar_hsa_circ_78057,RMVar_hsa_circ_191169 23659 RMVar_ID_23659 Human_SNP_ID_655663774 A-to-I Human chr19 - 2125480 2125480 2125480 AACCCCATCTCTACCTAAAAAATACAAAAATTAGCAGGGCTTGGTGTCGGGCGCCTGTAATCCCG AACCCCATCTCTACCTAAAAAATACAAAAATTCGCAGGGCTTGGTGTCGGGCGCCTGTAATCCCG T G AP3D1 Ensembl:ENSG00000065000 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1184297313 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_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_95127,RMVar_hsa_circ_111584,RMVar_hsa_circ_191166,RMVar_hsa_circ_127420,RMVar_hsa_circ_191167,RMVar_hsa_circ_191168,RMVar_hsa_circ_78057,RMVar_hsa_circ_191169 23660 RMVar_ID_23660 Human_SNP_ID_655667119 A-to-I Human chr19 - 2133936 2133936 2133936 GTCCGACTAATTTTTTTTATTTTAGGAGAGACAGGGTTTCACCATGTTGGTCAGGATGGTCTCGA GTCCGACTAATTTTTTTTATTTTAGGAGAGACGGGGTTTCACCATGTTGGTCAGGATGGTCTCGA T C AP3D1 Ensembl:ENSG00000065000 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs901480452 Functional Loss SNV dbSNP153 33..33 33 - - - 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 23661 RMVar_ID_23661 Human_SNP_ID_655667171 A-to-I Human chr19 - 2134084 2134080 2134084 TTTATTTTATTTATTTTTTGAGACAGAGTCTCACTCTGTCGCCATCTGGAGTACAATGTCGGCTC TTTATTTTATTTATTTTTTGAGACAGAGTCTC____TGTCGCCATCTGGAGTACAATGTCGGCTC AGAGT A AP3D1 Ensembl:ENSG00000065000 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1480176293 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_6730208,Human_RBP_ID_13409197,Human_RBP_ID_22477043 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 23662 RMVar_ID_23662 Human_SNP_ID_655667253 A-to-I Human chr19 - 2134364 2134364 2134364 CAGGCTGGAGAGCAGTAGCGCAATTGCAGCTCACTGCAGCCTCGACCTCCTAGGCTCAAGCGATC CAGGCTGGAGAGCAGTAGCGCAATTGCAGCTCGCTGCAGCCTCGACCTCCTAGGCTCAAGCGATC T C AP3D1 Ensembl:ENSG00000065000 Protein coding intron GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line - 24183664,31158229 RNA-Seq:(High) rs1450443313 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22477045,Human_RBP_ID_22720353,Human_RBP_ID_23175301,Human_RBP_ID_23309430 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 23663 RMVar_ID_23663 Human_SNP_ID_655667378 A-to-I Human chr19 - 2134739 2134739 2134739 AAATTAGCCGGGCGTGGTGGTGCGTGCCTATAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAA AAATTAGCCGGGCGTGGTGGTGCGTGCCTATACTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAA T G AP3D1 Ensembl:ENSG00000065000 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1367042033 Functional Loss SNV dbSNP153 33..33 33 - - - 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 23664 RMVar_ID_23664 Human_SNP_ID_655667490 A-to-I Human chr19 - 2135114 2135114 2135114 TCACTGCAACCTCTGCCTCCCAGGTTCAAGCAATTCTCCTGCGTCAGCCTCCCAAGTAGCTGGGA TCACTGCAACCTCTGCCTCCCAGGTTCAAGCAGTTCTCCTGCGTCAGCCTCCCAAGTAGCTGGGA T C AP3D1 Ensembl:ENSG00000065000 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs938310698 Functional Loss SNV dbSNP153 33..33 33 - - - 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 23665 RMVar_ID_23665 Human_SNP_ID_655667491 A-to-I Human chr19 - 2135118 2135118 2135118 TGGCTCACTGCAACCTCTGCCTCCCAGGTTCAAGCAATTCTCCTGCGTCAGCCTCCCAAGTAGCT TGGCTCACTGCAACCTCTGCCTCCCAGGTTCAGGCAATTCTCCTGCGTCAGCCTCCCAAGTAGCT T C AP3D1 Ensembl:ENSG00000065000 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1403564618 Functional Loss SNV dbSNP153 33..33 33 - - - 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 23666 RMVar_ID_23666 Human_SNP_ID_655667576 A-to-I Human chr19 - 2135454 2135454 2135454 TCGGCTCACCGCAACCTCTGCCTCCTGGGTTCAAGCGATTCTACTGCCTCAGCCTCCCGAGTAGC TCGGCTCACCGCAACCTCTGCCTCCTGGGTTCGAGCGATTCTACTGCCTCAGCCTCCCGAGTAGC T C AP3D1 Ensembl:ENSG00000065000 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs552384840 Functional Loss SNV dbSNP153 33..33 33 - - - 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 23667 RMVar_ID_23667 Human_SNP_ID_655667595 A-to-I Human chr19 - 2135517 2135517 2135517 TTTTGTTTTGTTTTGAGACTGAGTCTCACTCTATTGCCCAGGCTGGAGAGCAGTGGCGTGATGTC TTTTGTTTTGTTTTGAGACTGAGTCTCACTCTGTTGCCCAGGCTGGAGAGCAGTGGCGTGATGTC T C AP3D1 Ensembl:ENSG00000065000 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs971938036 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13409445 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 23668 RMVar_ID_23668 Human_SNP_ID_655667596 A-to-I Human chr19 - 2135522 2135518 2135522 TTTTGTTTTGTTTTGTTTTGAGACTGAGTCTCACTCTATTGCCCAGGCTGGAGAGCAGTGGCGTG TTTTGTTTTGTTTTGTTTTGAGACTGAGTCTC____TATTGCCCAGGCTGGAGAGCAGTGGCGTG AGAGT A AP3D1 Ensembl:ENSG00000065000 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1458842268 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_3565413 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 23669 RMVar_ID_23669 Human_SNP_ID_655667598 A-to-I Human chr19 - 2135522 2135522 2135522 TTTTGTTTTGTTTTGTTTTGAGACTGAGTCTCACTCTATTGCCCAGGCTGGAGAGCAGTGGCGTG TTTTGTTTTGTTTTGTTTTGAGACTGAGTCTCGCTCTATTGCCCAGGCTGGAGAGCAGTGGCGTG T C AP3D1 Ensembl:ENSG00000065000 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs983857479 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3565413 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 23670 RMVar_ID_23670 Human_SNP_ID_655669541 A-to-I Human chr19 - 2140932 2140932 2140932 CAACGTGGCGAAACCCCGTCTCTACCAAAAATACAAGAATTAGCTGGGCATGGTGGTGTGCCCCT CAACGTGGCGAAACCCCGTCTCTACCAAAAATGCAAGAATTAGCTGGGCATGGTGGTGTGCCCCT T C AP3D1 Ensembl:ENSG00000065000 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1049806714 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103983,RMVar_hsa_circ_191179,RMVar_hsa_circ_191183,RMVar_hsa_circ_86711 23671 RMVar_ID_23671 Human_SNP_ID_655676014 A-to-I Human chr19 - 2159330 2159330 2159330 CCTGTAATCCCGGCTGCTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCTGGGAGGCGGAGGTT CCTGTAATCCCGGCTGCTCGGGAGGCTGAGGCGGGAGAATCGCTTGAACCTGGGAGGCGGAGGTT T C AP3D1 Ensembl:ENSG00000065000 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1238944342 Functional Loss SNV dbSNP153 33..33 33 - - - 23672 RMVar_ID_23672 Human_SNP_ID_655681726 A-to-I Human chr19 + 2175755 2175755 2175755 AGGAGGCTGAGACGGGAAAATCGCTTGAACCCAGGAAGTGGAGGTTGCAGTGAGCCGAGACTGCG AGGAGGCTGAGACGGGAAAATCGCTTGAACCCGGGAAGTGGAGGTTGCAGTGAGCCGAGACTGCG A G DOT1L Ensembl:ENSG00000104885 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1315725500 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268349 23673 RMVar_ID_23673 Human_SNP_ID_655717330 A-to-I Human chr19 + 2271692 2271692 2271692 CTCCTGCAGCCCAGGCGTTGCCTGAGCTCAACACGGCCTAGGCCCAAGCTTTAGCGCTGCCGGGT CTCCTGCAGCCCAGGCGTTGCCTGAGCTCAACGCGGCCTAGGCCCAAGCTTTAGCGCTGCCGGGT A G AC005258.1,OAZ1 Ensembl:ENSG00000273734,Ensembl:ENSG00000104904 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs771391022 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123026,RMVar_hsa_circ_332875,RMVar_hsa_circ_317653,RMVar_hsa_circ_191247,RMVar_hsa_circ_191248 23674 RMVar_ID_23674 Human_SNP_ID_655735983 A-to-I Human chr19 - 2328076 2328076 2328076 TAGAGAGGCCATGTTGGCCAGGATGGTCTCAAACTCCTGGCCTCAAGCGATCTGCCTGCCTCAGC TAGAGAGGCCATGTTGGCCAGGATGGTCTCAAGCTCCTGGCCTCAAGCGATCTGCCTGCCTCAGC T C LSM7 Ensembl:ENSG00000130332 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1437049917 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100570,RMVar_hsa_circ_191256 23675 RMVar_ID_23675 Human_SNP_ID_655735984 A-to-I Human chr19 - 2328078 2328078 2328078 AGTAGAGAGGCCATGTTGGCCAGGATGGTCTCAAACTCCTGGCCTCAAGCGATCTGCCTGCCTCA AGTAGAGAGGCCATGTTGGCCAGGATGGTCTCGAACTCCTGGCCTCAAGCGATCTGCCTGCCTCA T C LSM7 Ensembl:ENSG00000130332 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs936020335 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100570,RMVar_hsa_circ_191256 23676 RMVar_ID_23676 Human_SNP_ID_655735993 A-to-I Human chr19 - 2328107 2328107 2328107 CACCACGCCCGGCTAATATTTGTATTTTTAGTAGAGAGGCCATGTTGGCCAGGATGGTCTCAAAC CACCACGCCCGGCTAATATTTGTATTTTTAGTGGAGAGGCCATGTTGGCCAGGATGGTCTCAAAC T C LSM7 Ensembl:ENSG00000130332 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1170149373 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13413595 RMVar_hsa_circ_100570,RMVar_hsa_circ_191256 23677 RMVar_ID_23677 Human_SNP_ID_655771633 A-to-I Human chr19 - 2420355 2420355 2420355 TCACTGTGACCTCCGCCTCCTGGGCTCAAGCAATTCTCCTGCCTCAGCCTCCGGAGTAGCTAGAA TCACTGTGACCTCCGCCTCCTGGGCTCAAGCAGTTCTCCTGCCTCAGCCTCCGGAGTAGCTAGAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1353869799 Functional Loss SNV dbSNP153 33..33 33 - - - 23678 RMVar_ID_23678 Human_SNP_ID_655771645 A-to-I Human chr19 - 2420398 2420398 2420398 TCACTCTGTTGCCCGGGCTGGAGTGCAGTGACATGATCTCGGCTCACTGTGACCTCCGCCTCCTG TCACTCTGTTGCCCGGGCTGGAGTGCAGTGACTTGATCTCGGCTCACTGTGACCTCCGCCTCCTG T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs996474412 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13415492,Human_RBP_ID_25392870 23679 RMVar_ID_23679 Human_SNP_ID_655771661 A-to-I Human chr19 - 2420440 2420440 2420440 AATCTGATGCCATTTTTTTTTTTTTTTTTTTGAGGTGGAGTCTCACTCTGTTGCCCGGGCTGGAG AATCTGATGCCATTTTTTTTTTTTTTTTTTTGTGGTGGAGTCTCACTCTGTTGCCCGGGCTGGAG T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1160029493 Functional Loss SNV dbSNP153 33..33 33 - - - 23680 RMVar_ID_23680 Human_SNP_ID_655775544 A-to-I Human chr19 - 2429185 2429185 2429185 TCACCCGGACCCGACTGGCTGGGCTTCGTGCTAGCGAGGGTTCTGGGGGTGGGTCTTGGTGATCT TCACCCGGACCCGACTGGCTGGGCTTCGTGCTGGCGAGGGTTCTGGGGGTGGGTCTTGGTGATCT T C LMNB2 Ensembl:ENSG00000176619 Protein coding intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1272549982 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_518178,Human_RBP_ID_4564984,Human_RBP_ID_6734144,Human_RBP_ID_17382721,Human_RBP_ID_23789530 Human_miRNA_ID_2469877,Human_miRNA_ID_2469878 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 23681 RMVar_ID_23681 Human_SNP_ID_655782149 A-to-I Human chr19 - 2448815 2448813 2448816 TTTGAAGTGGAGTCTGGCTGTCGCCAGGCTGGAGTGCAATGGCCCAATCTTGGCTCACAGCAACC TTTGAAGTGGAGTCTGGCTGTCGCCAGGCTG___TGCAATGGCCCAATCTTGGCTCACAGCAACC ACTC A LMNB2 Ensembl:ENSG00000176619 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1165459885 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_96966,RMVar_hsa_circ_191259 23682 RMVar_ID_23682 Human_SNP_ID_655782206 A-to-I Human chr19 - 2449029 2449029 2449029 CTAATTAGGCAGGCATAGTAGTATGTGTGCCTATAGTCCCAGCTATTGGGGCAGCTGAGACAGGA CTAATTAGGCAGGCATAGTAGTATGTGTGCCTGTAGTCCCAGCTATTGGGGCAGCTGAGACAGGA T C LMNB2 Ensembl:ENSG00000176619 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs920633885 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96966,RMVar_hsa_circ_191259 23683 RMVar_ID_23683 Human_SNP_ID_655782908 A-to-I Human chr19 - 2451192 2451192 2451192 CAGGCTGGAATGCAGTGGCACAATCTCCGCTCACTTCAACCTCTGCCTCCCGGATTCAGGCGATG CAGGCTGGAATGCAGTGGCACAATCTCCGCTCGCTTCAACCTCTGCCTCCCGGATTCAGGCGATG T C LMNB2 Ensembl:ENSG00000176619 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1247542797 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23175531 RMVar_hsa_circ_96966,RMVar_hsa_circ_191259 23684 RMVar_ID_23684 Human_SNP_ID_655803115 A-to-I Human chr19 - 2516393 2516393 2516393 ATGCTGAAACCCGTCTCTACTAAAAATACAAAAATTAGCTGGGCGTGGTGGCAGGCACCTGTAGT ATGCTGAAACCCGTCTCTACTAAAAATACAAACATTAGCTGGGCGTGGTGGCAGGCACCTGTAGT T G GNG7 Ensembl:ENSG00000176533 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1280454771 Functional Loss SNV dbSNP153 33..33 33 - - - 23685 RMVar_ID_23685 Human_SNP_ID_655830677 A-to-I Human chr19 - 2601023 2601023 2601023 TCAAGCGATCCTACCACTTCAGCCTCCCAAGTAGCTGGGAGCACAGGCACACACCACCACAACTG TCAAGCGATCCTACCACTTCAGCCTCCCAAGTTGCTGGGAGCACAGGCACACACCACCACAACTG T A GNG7 Ensembl:ENSG00000176533 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs992172343 Functional Loss SNV dbSNP153 33..33 33 - - - 23686 RMVar_ID_23686 Human_SNP_ID_655830875 A-to-I Human chr19 - 2601731 2601731 2601731 GGCTAATTTTTTTATAAAGACAGGGTCTCGCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCT GGCTAATTTTTTTATAAAGACAGGGTCTCGCCCTGTTGCTCAGGCTGGTCTCGAACTCCTGGGCT T G GNG7 Ensembl:ENSG00000176533 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256037836 Functional Loss SNV dbSNP153 33..33 33 - - - 23687 RMVar_ID_23687 Human_SNP_ID_655859650 A-to-I Human chr19 - 2696081 2696081 2696081 GCAATCTCGGCTCACTGCAACCTCCACCTCCCAGGTTCCAGTGATTCTCCTGCCTCAGCCTCCCG GCAATCTCGGCTCACTGCAACCTCCACCTCCCGGGTTCCAGTGATTCTCCTGCCTCAGCCTCCCG T C GNG7 Ensembl:ENSG00000176533 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs555670515 Functional Loss SNV dbSNP153 33..33 33 - - - 23688 RMVar_ID_23688 Human_SNP_ID_655859653 A-to-I Human chr19 - 2696088 2696088 2696088 CAGTGGTGCAATCTCGGCTCACTGCAACCTCCACCTCCCAGGTTCCAGTGATTCTCCTGCCTCAG CAGTGGTGCAATCTCGGCTCACTGCAACCTCCGCCTCCCAGGTTCCAGTGATTCTCCTGCCTCAG T C GNG7 Ensembl:ENSG00000176533 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1273227414 Functional Loss SNV dbSNP153 33..33 33 - - - 23689 RMVar_ID_23689 Human_SNP_ID_655890123 A-to-I Human chr19 + 2792365 2792365 2792365 TCTTTAATTTTTGGTAGAGATGAGGTCTTGCTATATTGCCCAGGCTGGTCTAGAACTCCTGAGCT TCTTTAATTTTTGGTAGAGATGAGGTCTTGCTGTATTGCCCAGGCTGGTCTAGAACTCCTGAGCT A G THOP1 Ensembl:ENSG00000172009 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1329302926 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25443009 RMVar_hsa_circ_52424,RMVar_hsa_circ_363211,RMVar_hsa_circ_305086,RMVar_hsa_circ_191285 23690 RMVar_ID_23690 Human_SNP_ID_655890640 A-to-I Human chr19 + 2794076 2794076 2794076 TCACTCTGTCGCCCAGGCTGGAGTGCAGTGGTACCATTTCAACTCGCTGCAACCTCCACCTCCCG TCACTCTGTCGCCCAGGCTGGAGTGCAGTGGTTCCATTTCAACTCGCTGCAACCTCCACCTCCCG A T THOP1 Ensembl:ENSG00000172009 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1269615299 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_52424,RMVar_hsa_circ_363211,RMVar_hsa_circ_305086,RMVar_hsa_circ_191285 23691 RMVar_ID_23691 Human_SNP_ID_655902203 A-to-I Human chr19 + 2830066 2830066 2830066 CCTGCCTCAGCCTCCGGAGTAGCTGGGACTACAGGCGCCCGCCACCATGCCCGGCTAATTTTTTA CCTGCCTCAGCCTCCGGAGTAGCTGGGACTACCGGCGCCCGCCACCATGCCCGGCTAATTTTTTA A C ZNF554 Ensembl:ENSG00000172006 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1282071206 Functional Loss SNV dbSNP153 33..33 33 - - - 23692 RMVar_ID_23692 Human_SNP_ID_655902449 A-to-I Human chr19 + 2830992 2830992 2830992 TTTGCCATGTTGGCCAGGGTGGTGTTGAACTCATGACCTCTAGTGATCCACCTACTTCCGCTTCC TTTGCCATGTTGGCCAGGGTGGTGTTGAACTCCTGACCTCTAGTGATCCACCTACTTCCGCTTCC A C ZNF554 Ensembl:ENSG00000172006 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs546849112 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13419074 23693 RMVar_ID_23693 Human_SNP_ID_655903772 A-to-I Human chr19 + 2835217 2835217 2835217 GTGGGAGGCAGGGTGCGGTGGCTCATGCCTATAATCCTAACACTTTAGGAGGCCGAGGCGGGTGG GTGGGAGGCAGGGTGCGGTGGCTCATGCCTATGATCCTAACACTTTAGGAGGCCGAGGCGGGTGG A G ZNF554 Ensembl:ENSG00000172006 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1009748930 Functional Loss SNV dbSNP153 33..33 33 - - - 23694 RMVar_ID_23694 Human_SNP_ID_655903961 A-to-I Human chr19 + 2835932 2835932 2835932 CTGTAGTCAGCCTTCATCTCCTGGACTCAAGCAATCCTCCCACCTCAGCCTCTCCGGTAGCTGGG CTGTAGTCAGCCTTCATCTCCTGGACTCAAGCTATCCTCCCACCTCAGCCTCTCCGGTAGCTGGG A T ZNF554 Ensembl:ENSG00000172006 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459584576 Functional Loss SNV dbSNP153 33..33 33 - - - 23695 RMVar_ID_23695 Human_SNP_ID_655904306 A-to-I Human chr19 + 2837075 2837075 2837075 AATTAGAAAGGAGTAGAATCTGGGCTGGGCACAGTGGCTCACACCTGTGATCCCAGCACTTTGAG AATTAGAAAGGAGTAGAATCTGGGCTGGGCACCGTGGCTCACACCTGTGATCCCAGCACTTTGAG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251129028 Functional Loss SNV dbSNP153 33..33 33 - - - 23696 RMVar_ID_23696 Human_SNP_ID_655904700 A-to-I Human chr19 + 2838597 2838597 2838597 ACCTCAGGTTGTCCACCCACCTCAGCCTCCCAAAGTGCTGGGATTAGAGGCGTGAGCCACCGAGC ACCTCAGGTTGTCCACCCACCTCAGCCTCCCACAGTGCTGGGATTAGAGGCGTGAGCCACCGAGC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1266841869 Functional Loss SNV dbSNP153 33..33 33 - - - 23697 RMVar_ID_23697 Human_SNP_ID_655917786 A-to-I Human chr19 + 2881446 2881446 2881446 AAAAATACAAAAAATTGGCCAGGCGTGGTGGCAGGCGCCTGTAATCCCAGCTACTTGGGAGGCTG AAAAATACAAAAAATTGGCCAGGCGTGGTGGCGGGCGCCTGTAATCCCAGCTACTTGGGAGGCTG A G ZNF556 Ensembl:ENSG00000172000 Protein coding 3'UTR GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs554635920 Functional Loss SNV dbSNP153 33..33 33 - - - 23698 RMVar_ID_23698 Human_SNP_ID_655934963 A-to-I Human chr19 - 2934284 2934284 2934284 AAGGAGTGTGGGAAAGCCTTCAGCTGTCCCTCATACTTTCGAGAACATGTCAGAACACACACTGG AAGGAGTGTGGGAAAGCCTTCAGCTGTCCCTCTTACTTTCGAGAACATGTCAGAACACACACTGG T A ZNF77 Ensembl:ENSG00000175691 Protein coding CDS GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs3746073 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2283 23699 RMVar_ID_23699 Human_SNP_ID_655934964 A-to-I Human chr19 - 2934284 2934284 2934284 AAGGAGTGTGGGAAAGCCTTCAGCTGTCCCTCATACTTTCGAGAACATGTCAGAACACACACTGG AAGGAGTGTGGGAAAGCCTTCAGCTGTCCCTCGTACTTTCGAGAACATGTCAGAACACACACTGG T C ZNF77 Ensembl:ENSG00000175691 Protein coding CDS GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs3746073 Functional Loss SNV dbSNP153,JSNP,HGVD 33..33 33 - - - GWAS_ID_2283 23700 RMVar_ID_23700 Human_SNP_ID_655934965 A-to-I Human chr19 - 2934284 2934284 2934284 AAGGAGTGTGGGAAAGCCTTCAGCTGTCCCTCATACTTTCGAGAACATGTCAGAACACACACTGG AAGGAGTGTGGGAAAGCCTTCAGCTGTCCCTCCTACTTTCGAGAACATGTCAGAACACACACTGG T G ZNF77 Ensembl:ENSG00000175691 Protein coding CDS GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs3746073 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2283 23701 RMVar_ID_23701 Human_SNP_ID_655935490 A-to-I Human chr19 - 2935781 2935781 2935781 AACTCCTGGACTCAAGCAGTCCACCCATCTCAACCTCCCAAAGTGCTGGGATTACAAGTGTGATT AACTCCTGGACTCAAGCAGTCCACCCATCTCAGCCTCCCAAAGTGCTGGGATTACAAGTGTGATT T C ZNF77 Ensembl:ENSG00000175691 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1392280451 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27466525 23702 RMVar_ID_23702 Human_SNP_ID_655937177 A-to-I Human chr19 - 2940634 2940634 2940634 GGAGACTCACTCTGTTGCTAGACTGGAGTGCAATGGCGCCATCTCGGCTCACTGCAACCTCTGCC GGAGACTCACTCTGTTGCTAGACTGGAGTGCAGTGGCGCCATCTCGGCTCACTGCAACCTCTGCC T C ZNF77 Ensembl:ENSG00000175691 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs999037335 Functional Loss SNV dbSNP153 33..33 33 - - - 23703 RMVar_ID_23703 Human_SNP_ID_655965407 A-to-I Human chr19 - 3020167 3020167 3020167 CATTGGCACGATCTCGGCTCACTGCAACCTCCACCTCCCGGGTTCAAGCGATTCTCCTGCCTCAG CATTGGCACGATCTCGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCAG T C TLE2 Ensembl:ENSG00000065717 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs922314786 Functional Loss SNV dbSNP153 33..33 33 - - - 23704 RMVar_ID_23704 Human_SNP_ID_655965424 A-to-I Human chr19 - 3020202 3020201 3020202 AGACAGAGTCTCGCTCTGTCACCCAGGCTGGAATGCATTGGCACGATCTCGGCTCACTGCAACCT AGACAGAGTCTCGCTCTGTCACCCAGGCTGGA_TGCATTGGCACGATCTCGGCTCACTGCAACCT AT A TLE2 Ensembl:ENSG00000065717 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1248565742 Functional Loss DEL dbSNP153 33..33 33 - - - 23705 RMVar_ID_23705 Human_SNP_ID_655965425 A-to-I Human chr19 - 3020202 3020202 3020202 AGACAGAGTCTCGCTCTGTCACCCAGGCTGGAATGCATTGGCACGATCTCGGCTCACTGCAACCT AGACAGAGTCTCGCTCTGTCACCCAGGCTGGAGTGCATTGGCACGATCTCGGCTCACTGCAACCT T C TLE2 Ensembl:ENSG00000065717 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs896973116 Functional Loss SNV dbSNP153 33..33 33 - - - 23706 RMVar_ID_23706 Human_SNP_ID_655965426 A-to-I Human chr19 - 3020202 3020202 3020202 AGACAGAGTCTCGCTCTGTCACCCAGGCTGGAATGCATTGGCACGATCTCGGCTCACTGCAACCT AGACAGAGTCTCGCTCTGTCACCCAGGCTGGACTGCATTGGCACGATCTCGGCTCACTGCAACCT T G TLE2 Ensembl:ENSG00000065717 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs896973116 Functional Loss SNV dbSNP153 33..33 33 - - - 23707 RMVar_ID_23707 Human_SNP_ID_656022518 A-to-I Human chr19 + 3194193 3194193 3194193 CCTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACCTGGCGAAAGCCTGTCTTTACTAAAAAAAT CCTGAGGTCAGGAGTTCGAGACCAGCCTGGCCCACCTGGCGAAAGCCTGTCTTTACTAAAAAAAT A C NCLN Ensembl:ENSG00000125912 Protein coding intron GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-Seq:(High) rs1350074098 Functional Loss SNV dbSNP153 33..33 33 - - - 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_307233,RMVar_hsa_circ_191316,RMVar_hsa_circ_191317,RMVar_hsa_circ_19211,RMVar_hsa_circ_274659,RMVar_hsa_circ_191319 23708 RMVar_ID_23708 Human_SNP_ID_656022530 A-to-I Human chr19 + 3194230 3194230 3194230 GGCGAAAGCCTGTCTTTACTAAAAAAATAGAAAAAGTTAGCCGGGCGCGGTGGCAGGTGCCTGTA GGCGAAAGCCTGTCTTTACTAAAAAAATAGAAGAAGTTAGCCGGGCGCGGTGGCAGGTGCCTGTA A G NCLN Ensembl:ENSG00000125912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1445034432 Functional Loss SNV dbSNP153 33..33 33 - - - 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_307233,RMVar_hsa_circ_191316,RMVar_hsa_circ_191317,RMVar_hsa_circ_19211,RMVar_hsa_circ_274659,RMVar_hsa_circ_191319 23709 RMVar_ID_23709 Human_SNP_ID_656022815 A-to-I Human chr19 + 3195164 3195164 3195164 AGATCTTGCCATTGCACTCCAGCCCGGGTGACAGTACGATACTCCGACTTGAAAAAAAAAAAAAT AGATCTTGCCATTGCACTCCAGCCCGGGTGACGGTACGATACTCCGACTTGAAAAAAAAAAAAAT A G NCLN Ensembl:ENSG00000125912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1281853752 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13423861 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_307233,RMVar_hsa_circ_191316,RMVar_hsa_circ_191317,RMVar_hsa_circ_19211,RMVar_hsa_circ_274659,RMVar_hsa_circ_191319 23710 RMVar_ID_23710 Human_SNP_ID_656022880 A-to-I Human chr19 + 3195329 3195329 3195329 TGGAGTGCAGTGGCACAATCTCGGCTCACTGCAAGCTCCACCTCCCGGGTTCGCGCCATTCTCCT TGGAGTGCAGTGGCACAATCTCGGCTCACTGCCAGCTCCACCTCCCGGGTTCGCGCCATTCTCCT A C NCLN Ensembl:ENSG00000125912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1174696536 Functional Loss SNV dbSNP153 33..33 33 - - - 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_307233,RMVar_hsa_circ_191316,RMVar_hsa_circ_191317,RMVar_hsa_circ_19211,RMVar_hsa_circ_274659,RMVar_hsa_circ_191319 23711 RMVar_ID_23711 Human_SNP_ID_656023000 A-to-I Human chr19 + 3195653 3195653 3195653 ATTTCAAAAGATTGTATTTTTAGGCCAGGCACAGTGGCTCATTGCCTGTAATCTTAGCACTTTGG ATTTCAAAAGATTGTATTTTTAGGCCAGGCACGGTGGCTCATTGCCTGTAATCTTAGCACTTTGG A G NCLN Ensembl:ENSG00000125912 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1237669874 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_771277,Human_RBP_ID_6739440,Human_RBP_ID_13542765 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_307233,RMVar_hsa_circ_191316,RMVar_hsa_circ_191317,RMVar_hsa_circ_19211,RMVar_hsa_circ_274659,RMVar_hsa_circ_191319 23712 RMVar_ID_23712 Human_SNP_ID_656029034 A-to-I Human chr19 + 3213072 3213072 3213072 CTACAGGCACCTGGCTAAATTTTTTTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGC CTACAGGCACCTGGCTAAATTTTTTTATTTTTGGTAGAGACAGGGTTTCACCATGTTGGCCAGGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1365284426 Functional Loss SNV dbSNP153 33..33 33 - - - 23713 RMVar_ID_23713 Human_SNP_ID_656030567 A-to-I Human chr19 + 3217821 3217821 3217821 GTTCAGGAGTTCAAAACCAGCCTAAGCAACATAGCAAGACCCCATCTCTACAAAAAATAAAAGAA GTTCAGGAGTTCAAAACCAGCCTAAGCAACATCGCAAGACCCCATCTCTACAAAAAATAAAAGAA A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1283134728 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18727314 23714 RMVar_ID_23714 Human_SNP_ID_656053384 A-to-I Human chr19 - 3295526 3295526 3295526 GAGGTGGTGGGGGTGGGGGTGGGGCACCTGGTATGTGTTGCGCGGGGTCCCGCCAACCTCAGCCC GAGGTGGTGGGGGTGGGGGTGGGGCACCTGGTTTGTGTTGCGCGGGGTCCCGCCAACCTCAGCCC T A - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs979144350 Functional Loss SNV dbSNP153 33..33 33 - - - 23715 RMVar_ID_23715 Human_SNP_ID_656053386 A-to-I Human chr19 + 3295527 3295527 3295527 GGCTGAGGTTGGCGGGACCCCGCGCAACACATACCAGGTGCCCCACCCCCACCCCCACCACCTCC GGCTGAGGTTGGCGGGACCCCGCGCAACACATTCCAGGTGCCCCACCCCCACCCCCACCACCTCC A T CELF5 Ensembl:ENSG00000161082 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs571373340 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2284,GWAS_ID_2285,GWAS_ID_2286,GWAS_ID_2287,GWAS_ID_2288 23716 RMVar_ID_23716 Human_SNP_ID_656082907 A-to-I Human chr19 + 3386557 3386557 3386557 GTTGGCCAGGGTGGTCTGGAACTCATGGCCTCAAGTGATCCGCCCTCCTCGGCCTCCCAAAGTGC GTTGGCCAGGGTGGTCTGGAACTCATGGCCTCGAGTGATCCGCCCTCCTCGGCCTCCCAAAGTGC A G NFIC Ensembl:ENSG00000141905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1273101525 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268967,RMVar_hsa_circ_327862,RMVar_hsa_circ_353774,RMVar_hsa_circ_335847 23717 RMVar_ID_23717 Human_SNP_ID_656085497 A-to-I Human chr19 + 3395387 3395387 3395387 ACTCTTTTGCCCAGACTGGAGTTCAGTGGTGCAATCACAGCTCACTGCAGCCTTCAACTCCCAGG ACTCTTTTGCCCAGACTGGAGTTCAGTGGTGCGATCACAGCTCACTGCAGCCTTCAACTCCCAGG A G NFIC Ensembl:ENSG00000141905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1302743625 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268967,RMVar_hsa_circ_327862,RMVar_hsa_circ_353774,RMVar_hsa_circ_335847 23718 RMVar_ID_23718 Human_SNP_ID_656091463 A-to-I Human chr19 + 3416069 3416069 3416069 CCTGTAGCCCCGGCTACTTGGGAAAAGAAGGCAAGAGAATCACTTGAGCCCAGGAGGTCGAGCCT CCTGTAGCCCCGGCTACTTGGGAAAAGAAGGCTAGAGAATCACTTGAGCCCAGGAGGTCGAGCCT A T NFIC Ensembl:ENSG00000141905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs865949153 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268967,RMVar_hsa_circ_327862,RMVar_hsa_circ_353774,RMVar_hsa_circ_335847 23719 RMVar_ID_23719 Human_SNP_ID_656094655 A-to-I Human chr19 + 3427133 3427133 3427133 TACTTTTAGTAGAGATGGGGTTTCACCGTGGTAGCCAGGATGGTCTCGATCTCCTGACCCTGTGA TACTTTTAGTAGAGATGGGGTTTCACCGTGGTGGCCAGGATGGTCTCGATCTCCTGACCCTGTGA A G NFIC Ensembl:ENSG00000141905 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs976674545 Functional Loss SNV dbSNP153 33..33 33 - - - 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 23720 RMVar_ID_23720 Human_SNP_ID_656094795 A-to-I Human chr19 + 3427662 3427662 3427662 ACCAGCCTGACCAACATGGTGAAACCGTCTCTACTAAAAATACAAAAATTAGTCGGGCATGTTGG ACCAGCCTGACCAACATGGTGAAACCGTCTCTTCTAAAAATACAAAAATTAGTCGGGCATGTTGG A T NFIC Ensembl:ENSG00000141905 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs969883498 Functional Loss SNV dbSNP153 33..33 33 - - - 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 23721 RMVar_ID_23721 Human_SNP_ID_656094808 A-to-I Human chr19 + 3427704 3427704 3427704 CAAAAATTAGTCGGGCATGTTGGCACACACCTATAATCCCAGCTAGTCGGGAGGCTGAGGCAGGA CAAAAATTAGTCGGGCATGTTGGCACACACCTGTAATCCCAGCTAGTCGGGAGGCTGAGGCAGGA A G NFIC Ensembl:ENSG00000141905 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1006814474 Functional Loss SNV dbSNP153 33..33 33 - - - 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 23722 RMVar_ID_23722 Human_SNP_ID_656094820 A-to-I Human chr19 + 3427752 3427752 3427752 GGGAGGCTGAGGCAGGAGAATCGCTTGAACCCAGGAGGCAGAGGTTGTGGTGAGCCGAGATTGTG GGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGGGAGGCAGAGGTTGTGGTGAGCCGAGATTGTG A G NFIC Ensembl:ENSG00000141905 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1295408218 Functional Loss SNV dbSNP153 33..33 33 - - - 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 23723 RMVar_ID_23723 Human_SNP_ID_656094930 A-to-I Human chr19 + 3428049 3428040 3428049 AAAATTAGCCAGGCGTGGAGGCACATGCCTGTAATCCCAGCTACCCGAGAGGCTGAGGCAGGAGA AAAATTAGCCAGGCGTGGAGGCAC_________ATCCCAGCTACCCGAGAGGCTGAGGCAGGAGA CATGCCTGTA C NFIC Ensembl:ENSG00000141905 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs914732655 Functional Loss DEL dbSNP153 25..33 33 - - - 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 23724 RMVar_ID_23724 Human_SNP_ID_656095000 A-to-I Human chr19 + 3428232 3428232 3428232 AAGAAGGAAGGGGCCAGGGCGCAGTGGCTTACACCTGTAATCCCAGTACTTTGGGAGGCCGAGTC AAGAAGGAAGGGGCCAGGGCGCAGTGGCTTACGCCTGTAATCCCAGTACTTTGGGAGGCCGAGTC A G NFIC Ensembl:ENSG00000141905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1345718361 Functional Loss SNV dbSNP153 33..33 33 - - - 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 23725 RMVar_ID_23725 Human_SNP_ID_656095019 A-to-I Human chr19 + 3428292 3428292 3428292 GAGTCAGGTGGATGACCTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGGCGAAACCCCAT GAGTCAGGTGGATGACCTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGCGAAACCCCAT A G NFIC Ensembl:ENSG00000141905 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1447135523 Functional Loss SNV dbSNP153 33..33 33 - - - 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 23726 RMVar_ID_23726 Human_SNP_ID_656095531 A-to-I Human chr19 + 3429397 3429397 3429397 GCCCAGGAGTTTGAGACCAGCCTGGGTAACATAGCAAGACCCTATCTCTACAAAAAGTAATAATA GCCCAGGAGTTTGAGACCAGCCTGGGTAACATGGCAAGACCCTATCTCTACAAAAAGTAATAATA A G NFIC Ensembl:ENSG00000141905 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1416036755 Functional Loss SNV dbSNP153 33..33 33 - - - 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 23727 RMVar_ID_23727 Human_SNP_ID_656096155 A-to-I Human chr19 + 3431494 3431494 3431494 GGGCTCGAGCTATCCTCCCGCCTCGGCCTCCCAAGTAGCTGGGACTACAGGTGTGCACCACCACG GGGCTCGAGCTATCCTCCCGCCTCGGCCTCCCGAGTAGCTGGGACTACAGGTGTGCACCACCACG A G NFIC Ensembl:ENSG00000141905 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1038265190 Functional Loss SNV dbSNP153 33..33 33 - - - 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 23728 RMVar_ID_23728 Human_SNP_ID_656096189 A-to-I Human chr19 + 3431678 3431678 3431678 GGCACAAGCCACCATACCCAGCTAATTTTCGTATTTTTTGTAGACACAGGGTTTCGCCATGTTGC GGCACAAGCCACCATACCCAGCTAATTTTCGTGTTTTTTGTAGACACAGGGTTTCGCCATGTTGC A G NFIC Ensembl:ENSG00000141905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs769217882 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13428682 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 23729 RMVar_ID_23729 Human_SNP_ID_656096193 A-to-I Human chr19 + 3431693 3431692 3431694 ACCCAGCTAATTTTCGTATTTTTTGTAGACACAGGGTTTCGCCATGTTGCCCGGGCTGATCTCAA ACCCAGCTAATTTTCGTATTTTTTGTAGACAC__GGTTTCGCCATGTTGCCCGGGCTGATCTCAA CAG C NFIC Ensembl:ENSG00000141905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1180893621 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_203859 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 23730 RMVar_ID_23730 Human_SNP_ID_656096195 A-to-I Human chr19 + 3431693 3431693 3431693 ACCCAGCTAATTTTCGTATTTTTTGTAGACACAGGGTTTCGCCATGTTGCCCGGGCTGATCTCAA ACCCAGCTAATTTTCGTATTTTTTGTAGACACGGGGTTTCGCCATGTTGCCCGGGCTGATCTCAA A G NFIC Ensembl:ENSG00000141905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1471552787 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_203859 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 23731 RMVar_ID_23731 Human_SNP_ID_656096200 A-to-I Human chr19 + 3431704 3431704 3431704 TTTCGTATTTTTTGTAGACACAGGGTTTCGCCATGTTGCCCGGGCTGATCTCAAACTCCTGAGCT TTTCGTATTTTTTGTAGACACAGGGTTTCGCCGTGTTGCCCGGGCTGATCTCAAACTCCTGAGCT A G NFIC Ensembl:ENSG00000141905 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1219195579 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_203859 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 23732 RMVar_ID_23732 Human_SNP_ID_656098192 A-to-I Human chr19 + 3437878 3437878 3437878 TTTTTGTATTTTTAGTAGAGACGGTTTTTACTATGTTGGCCAGGCTGGTCTTGAACTCCTGACCT TTTTTGTATTTTTAGTAGAGACGGTTTTTACTGTGTTGGCCAGGCTGGTCTTGAACTCCTGACCT A G NFIC Ensembl:ENSG00000141905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs757774307 Functional Loss SNV dbSNP153 33..33 33 - - - 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 23733 RMVar_ID_23733 Human_SNP_ID_656098194 A-to-I Human chr19 + 3437887 3437887 3437887 TTTTAGTAGAGACGGTTTTTACTATGTTGGCCAGGCTGGTCTTGAACTCCTGACCTCAAGTGATC TTTTAGTAGAGACGGTTTTTACTATGTTGGCCCGGCTGGTCTTGAACTCCTGACCTCAAGTGATC A C NFIC Ensembl:ENSG00000141905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1472337911 Functional Loss SNV dbSNP153 33..33 33 - - - 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 23734 RMVar_ID_23734 Human_SNP_ID_656099623 A-to-I Human chr19 + 3442480 3442480 3442480 TCGGCTCACTGCAGCCTCTGCCTTCCAGATTCAAGCAATTCTTCTGCTTCAGCCTCGCAAATAGC TCGGCTCACTGCAGCCTCTGCCTTCCAGATTCGAGCAATTCTTCTGCTTCAGCCTCGCAAATAGC A G NFIC Ensembl:ENSG00000141905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1387547905 Functional Loss SNV dbSNP153 33..33 33 - - - 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 23735 RMVar_ID_23735 Human_SNP_ID_656099624 A-to-I Human chr19 + 3442484 3442484 3442484 CTCACTGCAGCCTCTGCCTTCCAGATTCAAGCAATTCTTCTGCTTCAGCCTCGCAAATAGCTGGG CTCACTGCAGCCTCTGCCTTCCAGATTCAAGCGATTCTTCTGCTTCAGCCTCGCAAATAGCTGGG A G NFIC Ensembl:ENSG00000141905 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1281935051 Functional Loss SNV dbSNP153 33..33 33 - - - 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 23736 RMVar_ID_23736 Human_SNP_ID_656101280 A-to-I Human chr19 + 3448142 3448142 3448142 TAGCCCTGGCTGGAGTGTAGTGGCGTGATCTCAGCTCACTGCAACCTCTGCCTCCTGGGTTCAAG TAGCCCTGGCTGGAGTGTAGTGGCGTGATCTCCGCTCACTGCAACCTCTGCCTCCTGGGTTCAAG A C NFIC Ensembl:ENSG00000141905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1293741760 Functional Loss SNV dbSNP153 33..33 33 - - - 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 23737 RMVar_ID_23737 Human_SNP_ID_656101281 A-to-I Human chr19 + 3448142 3448142 3448142 TAGCCCTGGCTGGAGTGTAGTGGCGTGATCTCAGCTCACTGCAACCTCTGCCTCCTGGGTTCAAG TAGCCCTGGCTGGAGTGTAGTGGCGTGATCTCGGCTCACTGCAACCTCTGCCTCCTGGGTTCAAG A G NFIC Ensembl:ENSG00000141905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1293741760 Functional Loss SNV dbSNP153 33..33 33 - - - 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 23738 RMVar_ID_23738 Human_SNP_ID_656105261 A-to-I Human chr19 + 3460867 3460867 3460867 ATTCTCAAGGCCATGTGCAGTGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCCAAAGCAAAC ATTCTCAAGGCCATGTGCAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAAGCAAAC A G NFIC Ensembl:ENSG00000141905 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs974616372 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17568308 23739 RMVar_ID_23739 Human_SNP_ID_656105285 A-to-I Human chr19 + 3460978 3460978 3460978 GAAACCCCGTTTCTACCAAAAATACAAAAATTAGCTGGGTGTGATGGCGCATGCGTGTAATCCTA GAAACCCCGTTTCTACCAAAAATACAAAAATTTGCTGGGTGTGATGGCGCATGCGTGTAATCCTA A T NFIC Ensembl:ENSG00000141905 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs559220612 Functional Loss SNV dbSNP153 33..33 33 - - - 23740 RMVar_ID_23740 Human_SNP_ID_656105620 A-to-I Human chr19 + 3462120 3462120 3462120 GATTGAGTTCCAGACTGGGAGTGCTGGCTCACACCTGTAATTCCAGCACTTTGGGAGGCCGAGGA GATTGAGTTCCAGACTGGGAGTGCTGGCTCACCCCTGTAATTCCAGCACTTTGGGAGGCCGAGGA A C NFIC Ensembl:ENSG00000141905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs912525843 Functional Loss SNV dbSNP153 33..33 33 - - - 23741 RMVar_ID_23741 Human_SNP_ID_656105621 A-to-I Human chr19 + 3462120 3462120 3462120 GATTGAGTTCCAGACTGGGAGTGCTGGCTCACACCTGTAATTCCAGCACTTTGGGAGGCCGAGGA GATTGAGTTCCAGACTGGGAGTGCTGGCTCACGCCTGTAATTCCAGCACTTTGGGAGGCCGAGGA A G NFIC Ensembl:ENSG00000141905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs912525843 Functional Loss SNV dbSNP153 33..33 33 - - - 23742 RMVar_ID_23742 Human_SNP_ID_656107050 A-to-I Human chr19 + 3466309 3466309 3466309 TTGACCAAAGCTAAGACAATAGCCAGATGGTTAGTGGGGCAGCCAGGCAGGGAGGACCCAGGGCT TTGACCAAAGCTAAGACAATAGCCAGATGGTTGGTGGGGCAGCCAGGCAGGGAGGACCCAGGGCT A G NFIC Ensembl:ENSG00000141905 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1215757321 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_140224,Human_RBP_ID_6742485,Human_RBP_ID_13428831,Human_RBP_ID_18303404 23743 RMVar_ID_23743 Human_SNP_ID_656117411 A-to-I Human chr19 - 3501709 3501708 3501709 ATCGATCATCCTCTCACCCCACAGCCTCCCAAAGTGCCAGGATTACAGGTATGAGCCACCACTCC ATCGATCATCCTCTCACCCCACAGCCTCCCAA_GTGCCAGGATTACAGGTATGAGCCACCACTCC CT C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879060766 Functional Loss DEL dbSNP153 33..33 33 - - - 23744 RMVar_ID_23744 Human_SNP_ID_656117429 A-to-I Human chr19 - 3501767 3501766 3501767 TTCTGTTGAGACGGGGGCTTACCACATTGCCCAGGCTGGTCTTGGAATCTTGGGCTCAATCGATC TTCTGTTGAGACGGGGGCTTACCACATTGCCC_GGCTGGTCTTGGAATCTTGGGCTCAATCGATC CT C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs775412117 Functional Loss DEL dbSNP153 33..33 33 - - - 23745 RMVar_ID_23745 Human_SNP_ID_656117470 A-to-I Human chr19 - 3501883 3501883 3501883 TCAACTCACTGTAACCTGTGTCTCCCAGGCTCAAGCGATTCTCCTGCCTCAGCCACCCAAGTAGC TCAACTCACTGTAACCTGTGTCTCCCAGGCTCCAGCGATTCTCCTGCCTCAGCCACCCAAGTAGC T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1233037246 Functional Loss SNV dbSNP153 33..33 33 - - - 23746 RMVar_ID_23746 Human_SNP_ID_656117568 A-to-I Human chr19 - 3502226 3502226 3502226 TTGGCCATGCTGGTCTTGAACTCCTGACCACAAGTGATCCACCTGCCTTGGCCTCCCAAAGTGCT TTGGCCATGCTGGTCTTGAACTCCTGACCACAGGTGATCCACCTGCCTTGGCCTCCCAAAGTGCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1568225251 Functional Loss SNV dbSNP153 33..33 33 - - - 23747 RMVar_ID_23747 Human_SNP_ID_656120384 A-to-I Human chr19 - 3511500 3511500 3511500 CAGGGTCTCCCTATGTTGCCCGGGCTGGTTTCAAACTCCTGGGCTCAAGCAATCCTCCTGCTGAG CAGGGTCTCCCTATGTTGCCCGGGCTGGTTTCCAACTCCTGGGCTCAAGCAATCCTCCTGCTGAG T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1252689241 Functional Loss SNV dbSNP153 33..33 33 - - - 23748 RMVar_ID_23748 Human_SNP_ID_656121964 A-to-I Human chr19 - 3517376 3517376 3517376 AGCCAGGATTTTTATTTTTGAGACCGGGTCTCACTCTGTCACCTAGGCTGGAGAGCAGTGGTGCA AGCCAGGATTTTTATTTTTGAGACCGGGTCTCGCTCTGTCACCTAGGCTGGAGAGCAGTGGTGCA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1000226158 Functional Loss SNV dbSNP153 33..33 33 - - - 23749 RMVar_ID_23749 Human_SNP_ID_656122028 A-to-I Human chr19 - 3517641 3517641 3517641 TCTTTTTGCCCAGGCTGGAGTGCAGTGGTGCAATCTCGGCACACTGCAACCTCTGCCTCCCGGGT TCTTTTTGCCCAGGCTGGAGTGCAGTGGTGCAGTCTCGGCACACTGCAACCTCTGCCTCCCGGGT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1378597235 Functional Loss SNV dbSNP153 33..33 33 - - - 23750 RMVar_ID_23750 Human_SNP_ID_656122182 A-to-I Human chr19 - 3518117 3518117 3518117 CTAGCTACTAGGGAGGCTGAGGCAGGTGAATCACTTGAACCTGGAAGGCGGAGGTTGCAGTGAGC CTAGCTACTAGGGAGGCTGAGGCAGGTGAATCCCTTGAACCTGGAAGGCGGAGGTTGCAGTGAGC T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1422186946 Functional Loss SNV dbSNP153 33..33 33 - - - 23751 RMVar_ID_23751 Human_SNP_ID_656122373 A-to-I Human chr19 - 3518823 3518823 3518823 CTCTCGCTCTGTCGCCCAGGCTGGAATGCAGTAGTTTGATCATGGTTCACTGCAGCCTCCACCTC CTCTCGCTCTGTCGCCCAGGCTGGAATGCAGTGGTTTGATCATGGTTCACTGCAGCCTCCACCTC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1310838359 Functional Loss SNV dbSNP153 33..33 33 - - - 23752 RMVar_ID_23752 Human_SNP_ID_656130348 A-to-I Human chr19 - 3540017 3540017 3540017 GAACTCCTGGGCTCAAGTGATCCTCCTGTCTTAGCCTTCCAAAGTGCTGGGATTACAGGTGTGGG GAACTCCTGGGCTCAAGTGATCCTCCTGTCTTCGCCTTCCAAAGTGCTGGGATTACAGGTGTGGG T G MFSD12 Ensembl:ENSG00000161091 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs1379242726 Functional Loss SNV dbSNP153 33..33 33 - - - 23753 RMVar_ID_23753 Human_SNP_ID_656130354 A-to-I Human chr19 - 3540035 3540035 3540035 GTTGCTCAGGCTGGTCTTGAACTCCTGGGCTCAAGTGATCCTCCTGTCTTAGCCTTCCAAAGTGC GTTGCTCAGGCTGGTCTTGAACTCCTGGGCTCCAGTGATCCTCCTGTCTTAGCCTTCCAAAGTGC T G MFSD12 Ensembl:ENSG00000161091 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs966846546 Functional Loss SNV dbSNP153 33..33 33 - - - 23754 RMVar_ID_23754 Human_SNP_ID_656130369 A-to-I Human chr19 - 3540069 3540069 3540069 AAAAAAAAAAAAGAAAAGAGATGGGTCTCACTATGTTGCTCAGGCTGGTCTTGAACTCCTGGGCT AAAAAAAAAAAAGAAAAGAGATGGGTCTCACTGTGTTGCTCAGGCTGGTCTTGAACTCCTGGGCT T C MFSD12 Ensembl:ENSG00000161091 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910004511 Functional Loss SNV dbSNP153 33..33 33 - - - 23755 RMVar_ID_23755 Human_SNP_ID_656130434 A-to-I Human chr19 - 3540129 3540129 3540129 AGATTGCGCCACTGCACCCTAGCCTGGGCAACAGTATGAGACTGTCTCAAAAAAAAAAAAAAAAA AGATTGCGCCACTGCACCCTAGCCTGGGCAACGGTATGAGACTGTCTCAAAAAAAAAAAAAAAAA T C MFSD12 Ensembl:ENSG00000161091 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1385569879 Functional Loss SNV dbSNP153 33..33 33 - - - 23756 RMVar_ID_23756 Human_SNP_ID_656130435 A-to-I Human chr19 - 3540131 3540131 3540131 CAAGATTGCGCCACTGCACCCTAGCCTGGGCAACAGTATGAGACTGTCTCAAAAAAAAAAAAAAA CAAGATTGCGCCACTGCACCCTAGCCTGGGCAGCAGTATGAGACTGTCTCAAAAAAAAAAAAAAA T C MFSD12 Ensembl:ENSG00000161091 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1345004660 Functional Loss SNV dbSNP153 33..33 33 - - - 23757 RMVar_ID_23757 Human_SNP_ID_656130460 A-to-I Human chr19 - 3540240 3540240 3540240 AAAAAAACAAAAATTAGCTGGGCATGTGGCACAAACCTGTAGTCCTAGCTACTCAGAAGGCTTGA AAAAAAACAAAAATTAGCTGGGCATGTGGCACGAACCTGTAGTCCTAGCTACTCAGAAGGCTTGA T C MFSD12 Ensembl:ENSG00000161091 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs962655692 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1188811,Human_RBP_ID_17567497 23758 RMVar_ID_23758 Human_SNP_ID_656130514 A-to-I Human chr19 - 3540318 3540318 3540318 GGGAGTTGGAGGTTGCAGTGAGCCAAGATTGCACCATTGCGTTCCAGTCTTGCGACAAGAGTGAG GGGAGTTGGAGGTTGCAGTGAGCCAAGATTGCGCCATTGCGTTCCAGTCTTGCGACAAGAGTGAG T C MFSD12 Ensembl:ENSG00000161091 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs545188770 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13435091 23759 RMVar_ID_23759 Human_SNP_ID_656130515 A-to-I Human chr19 - 3540326 3540326 3540326 TCGAACCAGGGAGTTGGAGGTTGCAGTGAGCCAAGATTGCACCATTGCGTTCCAGTCTTGCGACA TCGAACCAGGGAGTTGGAGGTTGCAGTGAGCCGAGATTGCACCATTGCGTTCCAGTCTTGCGACA T C MFSD12 Ensembl:ENSG00000161091 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs566558648 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13435091 23760 RMVar_ID_23760 Human_SNP_ID_656130654 A-to-I Human chr19 - 3540551 3540551 3540551 TAAATTTTTTATAGAGATGGGGTCTCACAGCTAGGCGCGGTGCCTCACGCCTGTAATCCCAGCAC TAAATTTTTTATAGAGATGGGGTCTCACAGCTGGGCGCGGTGCCTCACGCCTGTAATCCCAGCAC T C MFSD12 Ensembl:ENSG00000161091 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1055164168 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13435093 23761 RMVar_ID_23761 Human_SNP_ID_656130718 A-to-I Human chr19 - 3540717 3540717 3540717 GAGCCACCATTCCCGGCTAATTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGTCAGGC GAGCCACCATTCCCGGCTAATTTTGTATTTTTGGTAGAGACGGGGTTTCACCATGTTGGTCAGGC T C MFSD12 Ensembl:ENSG00000161091 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs963652279 Functional Loss SNV dbSNP153 33..33 33 - - - 23762 RMVar_ID_23762 Human_SNP_ID_656130729 A-to-I Human chr19 - 3540757 3540757 3540757 CTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCATGAGCCACCATTCCCGGCTAATTTTG CTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTGCAGGCATGAGCCACCATTCCCGGCTAATTTTG T C MFSD12 Ensembl:ENSG00000161091 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1410015740 Functional Loss SNV dbSNP153 33..33 33 - - - 23763 RMVar_ID_23763 Human_SNP_ID_656130828 A-to-I Human chr19 - 3541006 3541006 3541006 CGCCACCACAACCAGCTAATTTTTGTACTTTTAGTACAGATGGGGTTTCACTACCTTGGCCAGGT CGCCACCACAACCAGCTAATTTTTGTACTTTTGGTACAGATGGGGTTTCACTACCTTGGCCAGGT T C MFSD12 Ensembl:ENSG00000161091 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1302663958 Functional Loss SNV dbSNP153 33..33 33 - - - 23764 RMVar_ID_23764 Human_SNP_ID_656130854 A-to-I Human chr19 - 3541228 3541061 3541228 AGGCTCAAGCGATCCTCCTACCTCAGCCTCCCAAGTAGCTGGCATTACAGGCACGTGCCGCCATG AGGCTCAAGCGATCCTCCTACCTCAGCCTCCC_________________________________ CGGGAGGCTGAGGCAGGAGAATCGCTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCCGAGATCAGGCCACTGCACTCCAGCCTGGGTGACAGAGCAAGACTCTGTCTCAAAAAAAAAAAAAAAAAATCAACCAGGCATGGCGGCACGTGCCTGTAATGCCAGCTACTT C MFSD12 Ensembl:ENSG00000161091 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1568247941 Functional Loss DEL dbSNP153 33..65 33 - - - 23765 RMVar_ID_23765 Human_SNP_ID_656130933 A-to-I Human chr19 - 3541214 3541214 3541214 CTCCTACCTCAGCCTCCCAAGTAGCTGGCATTACAGGCACGTGCCGCCATGCCTGGTTGATTTTT CTCCTACCTCAGCCTCCCAAGTAGCTGGCATTGCAGGCACGTGCCGCCATGCCTGGTTGATTTTT T C MFSD12 Ensembl:ENSG00000161091 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1003980980 Functional Loss SNV dbSNP153 33..33 33 - - - 23766 RMVar_ID_23766 Human_SNP_ID_656130939 A-to-I Human chr19 - 3541228 3541228 3541228 AGGCTCAAGCGATCCTCCTACCTCAGCCTCCCAAGTAGCTGGCATTACAGGCACGTGCCGCCATG AGGCTCAAGCGATCCTCCTACCTCAGCCTCCCGAGTAGCTGGCATTACAGGCACGTGCCGCCATG T C MFSD12 Ensembl:ENSG00000161091 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1313473741 Functional Loss SNV dbSNP153 33..33 33 - - - 23767 RMVar_ID_23767 Human_SNP_ID_656131181 A-to-I Human chr19 - 3541846 3541846 3541846 CGAGATTGCGTCACTGCACTCCAGCCTGGGTGAGAGAGCGAGACTCTGTCTCAACACAAACAAAA CGAGATTGCGTCACTGCACTCCAGCCTGGGTGGGAGAGCGAGACTCTGTCTCAACACAAACAAAA T C MFSD12 Ensembl:ENSG00000161091 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1160051863 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6745927 23768 RMVar_ID_23768 Human_SNP_ID_656131402 A-to-I Human chr19 - 3542598 3542598 3542598 GGGGCGGGGGGCACCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACCCA GGGGCGGGGGGCACCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCA T C MFSD12 Ensembl:ENSG00000161091 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1409059507 Functional Loss SNV dbSNP153 33..33 33 - - - 23769 RMVar_ID_23769 Human_SNP_ID_656131406 A-to-I Human chr19 - 3542618 3542618 3542618 ATTAAGCCAGGCATGGTGTGGGGGCGGGGGGCACCTGTAATCCCAGCTACTCAGGAGGCTGAGGC ATTAAGCCAGGCATGGTGTGGGGGCGGGGGGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGC T C MFSD12 Ensembl:ENSG00000161091 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1207176343 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26473271 23770 RMVar_ID_23770 Human_SNP_ID_656132762 A-to-I Human chr19 - 3544682 3544663 3544682 CCTGACTCCTGACAGCCTCCTGCACCTGTGCAAGGGAACTGTGGGGACGCACGAGGATGCCCCCC CCTGACTCCTGACAGCCTCCTGCACCTGTGCA___________________CGAGGATGCCCCCC GTGCGTCCCCACAGTTCCCT G MFSD12 Ensembl:ENSG00000161091 Protein coding intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs763675940 Functional Loss DEL dbSNP153 33..51 33 - - - Human_RBP_ID_5585610,Human_RBP_ID_27467138 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 23771 RMVar_ID_23771 Human_SNP_ID_656132778 A-to-I Human chr19 - 3544682 3544682 3544682 CCTGACTCCTGACAGCCTCCTGCACCTGTGCAAGGGAACTGTGGGGACGCACGAGGATGCCCCCC CCTGACTCCTGACAGCCTCCTGCACCTGTGCAGGGGAACTGTGGGGACGCACGAGGATGCCCCCC T C MFSD12 Ensembl:ENSG00000161091 Protein coding intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1257376682 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5585610,Human_RBP_ID_27467138 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 23772 RMVar_ID_23772 Human_SNP_ID_656135516 A-to-I Human chr19 - 3549489 3549489 3549489 CGAACTCCTGACCTCAGTGATCTGCCTGCCTCAGCCTCCCAAAGTGCTGAGATTACAGGCGTGAG CGAACTCCTGACCTCAGTGATCTGCCTGCCTCGGCCTCCCAAAGTGCTGAGATTACAGGCGTGAG T C MFSD12 Ensembl:ENSG00000161091 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs866191368 Functional Loss SNV dbSNP153 33..33 33 - - - 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 23773 RMVar_ID_23773 Human_SNP_ID_656136025 A-to-I Human chr19 - 3550669 3550669 3550669 TTTAAAGTTTTTGTAGGCTGGGCATGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGT TTTAAAGTTTTTGTAGGCTGGGCATGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGT T C MFSD12 Ensembl:ENSG00000161091 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs568431545 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5585619 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 23774 RMVar_ID_23774 Human_SNP_ID_656136756 A-to-I Human chr19 - 3552535 3552535 3552535 GGGAGGCAGAGGCTGCAATGAGCTGAGATCGCACCACTGCACTCCAGCCTGGGCAACAGAGCGAG GGGAGGCAGAGGCTGCAATGAGCTGAGATCGCGCCACTGCACTCCAGCCTGGGCAACAGAGCGAG T C MFSD12 Ensembl:ENSG00000161091 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1189408477 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127723,RMVar_hsa_circ_191358,RMVar_hsa_circ_100402,RMVar_hsa_circ_191364,RMVar_hsa_circ_96964,RMVar_hsa_circ_191366 23775 RMVar_ID_23775 Human_SNP_ID_656137339 A-to-I Human chr19 - 3554252 3554252 3554252 TTAAATTTTTAGTAGAGGCAAGGTTTCACCATATTGTCCAGGCTGGGCTTGAACCGCTGACCTCA TTAAATTTTTAGTAGAGGCAAGGTTTCACCATGTTGTCCAGGCTGGGCTTGAACCGCTGACCTCA T C MFSD12 Ensembl:ENSG00000161091 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1358373672 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127723,RMVar_hsa_circ_191358,RMVar_hsa_circ_100402,RMVar_hsa_circ_191364,RMVar_hsa_circ_96964,RMVar_hsa_circ_191366 23776 RMVar_ID_23776 Human_SNP_ID_656137375 A-to-I Human chr19 - 3554374 3554374 3554374 GGAGTGCAGTAGCGGGATCTCGGCTCACTGCAACCTTCGCCTCCTGAGTTCAAAGGATTCTCGTG GGAGTGCAGTAGCGGGATCTCGGCTCACTGCAGCCTTCGCCTCCTGAGTTCAAAGGATTCTCGTG T C MFSD12 Ensembl:ENSG00000161091 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs976423536 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127723,RMVar_hsa_circ_191358,RMVar_hsa_circ_100402,RMVar_hsa_circ_191364,RMVar_hsa_circ_96964,RMVar_hsa_circ_191366 23777 RMVar_ID_23777 Human_SNP_ID_656137625 A-to-I Human chr19 - 3555176 3555176 3555176 TGAACCCGGGAGGCAGAGGCTGTAGTCAGCCAAGATCGCGCCACTGCACTCCAGACACAGCGAGA TGAACCCGGGAGGCAGAGGCTGTAGTCAGCCAGGATCGCGCCACTGCACTCCAGACACAGCGAGA T C MFSD12 Ensembl:ENSG00000161091 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1246556644 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127723,RMVar_hsa_circ_191358,RMVar_hsa_circ_100402,RMVar_hsa_circ_191364,RMVar_hsa_circ_96964,RMVar_hsa_circ_191366 23778 RMVar_ID_23778 Human_SNP_ID_656138920 A-to-I Human chr19 + 3558816 3558804 3558817 AATCTTCAGGGCTCAAGTAATCCTCCTGTCTCAGCCTCCCAGGTAGCTGGGACTACAGGCACGCA AATCTTCAGGGCTCAAGTAAT_____________CCTCCCAGGTAGCTGGGACTACAGGCACGCA TCCTCCTGTCTCAG T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs759356333 Functional Loss DEL dbSNP153 22..34 33 - - - 23779 RMVar_ID_23779 Human_SNP_ID_656141582 A-to-I Human chr19 - 3567187 3567187 3567187 CAGCTCACTGCAACCTCGAACTCCTGGGCTCAAGTGATTCTCCTGCTTCAGCCTCTCGAGCAGTT CAGCTCACTGCAACCTCGAACTCCTGGGCTCAGGTGATTCTCCTGCTTCAGCCTCTCGAGCAGTT T C MFSD12 Ensembl:ENSG00000161091 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs970983789 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1937608,Human_Splice_Rec_1937609,Human_Splice_Rec_1937622,Human_Splice_Rec_1937623 23780 RMVar_ID_23780 Human_SNP_ID_656143018 A-to-I Human chr19 - 3572013 3572013 3572013 CGGCTCACTGCAACCTCTGCCTCCCGGGTTCAAGCAATTCTCTGCCTCACCCTCCCGAGTAGCTG CGGCTCACTGCAACCTCTGCCTCCCGGGTTCAGGCAATTCTCTGCCTCACCCTCCCGAGTAGCTG T C MFSD12 Ensembl:ENSG00000161091 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs549702175 Functional Loss SNV dbSNP153 33..33 33 - - - 23781 RMVar_ID_23781 Human_SNP_ID_656144539 A-to-I Human chr19 + 3575782 3575782 3575782 TGGCCAACATAGTGAAACCCTCCCCCTCTACTAAAAATACAAAAATTACCTGGGCGTGGTGGCGG TGGCCAACATAGTGAAACCCTCCCCCTCTACTGAAAATACAAAAATTACCTGGGCGTGGTGGCGG A G HMG20B Ensembl:ENSG00000064961 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1482234246 Functional Loss SNV dbSNP153 33..33 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 23782 RMVar_ID_23782 Human_SNP_ID_656162284 A-to-I Human chr19 - 3626685 3626685 3626685 GGCCGAAGGCGGCAGAGTCAGAGCGGGAGCCGAAGTCGGAGCAGGAGCCATGGGCGGCGAAACCG GGCCGAAGGCGGCAGAGTCAGAGCGGGAGCCGCAGTCGGAGCAGGAGCCATGGGCGGCGAAACCG T G CACTIN Ensembl:ENSG00000105298 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs766269170 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4557911,Human_RBP_ID_9381667,Human_RBP_ID_26337045 Human_Splice_Rec_1937805,Human_Splice_Rec_1937823,Human_Splice_Rec_1937845,Human_Splice_Rec_1937863 23783 RMVar_ID_23783 Human_SNP_ID_656169837 A-to-I Human chr19 - 3647764 3647764 3647764 TTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGATCT TTTTGTATTTTTAGTAGAGATGGGGTTTCACCGTGTTGGCCAGGCTGGTCTTGAACTCCTGATCT T C PIP5K1C Ensembl:ENSG00000186111 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1389691371 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_52619,RMVar_hsa_circ_45431,RMVar_hsa_circ_31064,RMVar_hsa_circ_126905,RMVar_hsa_circ_18282,RMVar_hsa_circ_15140,RMVar_hsa_circ_101823,RMVar_hsa_circ_191378,RMVar_hsa_circ_191379 23784 RMVar_ID_23784 Human_SNP_ID_656169838 A-to-I Human chr19 - 3647767 3647767 3647767 AATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGA AATTTTTGTATTTTTAGTAGAGATGGGGTTTCTCCATGTTGGCCAGGCTGGTCTTGAACTCCTGA T A PIP5K1C Ensembl:ENSG00000186111 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs150635233 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_52619,RMVar_hsa_circ_45431,RMVar_hsa_circ_31064,RMVar_hsa_circ_126905,RMVar_hsa_circ_18282,RMVar_hsa_circ_15140,RMVar_hsa_circ_101823,RMVar_hsa_circ_191378,RMVar_hsa_circ_191379 23785 RMVar_ID_23785 Human_SNP_ID_656169839 A-to-I Human chr19 - 3647767 3647767 3647767 AATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGA AATTTTTGTATTTTTAGTAGAGATGGGGTTTCGCCATGTTGGCCAGGCTGGTCTTGAACTCCTGA T C PIP5K1C Ensembl:ENSG00000186111 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs150635233 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_52619,RMVar_hsa_circ_45431,RMVar_hsa_circ_31064,RMVar_hsa_circ_126905,RMVar_hsa_circ_18282,RMVar_hsa_circ_15140,RMVar_hsa_circ_101823,RMVar_hsa_circ_191378,RMVar_hsa_circ_191379 23786 RMVar_ID_23786 Human_SNP_ID_656169987 A-to-I Human chr19 - 3648205 3648205 3648205 CAGCCTGGGCAACATAGCAAGACCCCATCTCTACAAAATATCAAAAAATTAGCTGAGCGTGGTGG CAGCCTGGGCAACATAGCAAGACCCCATCTCTGCAAAATATCAAAAAATTAGCTGAGCGTGGTGG T C PIP5K1C Ensembl:ENSG00000186111 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1405877946 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_52619,RMVar_hsa_circ_45431,RMVar_hsa_circ_31064,RMVar_hsa_circ_126905,RMVar_hsa_circ_18282,RMVar_hsa_circ_15140,RMVar_hsa_circ_101823,RMVar_hsa_circ_191378,RMVar_hsa_circ_191379 23787 RMVar_ID_23787 Human_SNP_ID_656169998 A-to-I Human chr19 - 3648250 3648250 3648250 GGGAGGCCGAGGCGGGAGGATTGCTTGAGCCCAGGAGTTTGAGACCAGCCTGGGCAACATAGCAA GGGAGGCCGAGGCGGGAGGATTGCTTGAGCCCTGGAGTTTGAGACCAGCCTGGGCAACATAGCAA T A PIP5K1C Ensembl:ENSG00000186111 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs369117116 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_52619,RMVar_hsa_circ_45431,RMVar_hsa_circ_31064,RMVar_hsa_circ_126905,RMVar_hsa_circ_18282,RMVar_hsa_circ_15140,RMVar_hsa_circ_101823,RMVar_hsa_circ_191378,RMVar_hsa_circ_191379 23788 RMVar_ID_23788 Human_SNP_ID_656170106 A-to-I Human chr19 - 3648541 3648541 3648541 CCACAGGTGGGCGCCCGGGTCTGCAGCCCCACAGGTGGGCGCCCGGGTCTGCAGCCCCACAGGTG CCACAGGTGGGCGCCCGGGTCTGCAGCCCCACGGGTGGGCGCCCGGGTCTGCAGCCCCACAGGTG T C PIP5K1C Ensembl:ENSG00000186111 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs922284546 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_52619,RMVar_hsa_circ_45431,RMVar_hsa_circ_31064,RMVar_hsa_circ_126905,RMVar_hsa_circ_18282,RMVar_hsa_circ_15140,RMVar_hsa_circ_101823,RMVar_hsa_circ_191378,RMVar_hsa_circ_191379 23789 RMVar_ID_23789 Human_SNP_ID_656181434 A-to-I Human chr19 - 3682462 3682462 3682462 TTGCTCGGTCTGGTCTGGAATTCCTGGGCTCAAGCAATCCTCCCACCTCGGCCTCCAAGTGTGCT TTGCTCGGTCTGGTCTGGAATTCCTGGGCTCATGCAATCCTCCCACCTCGGCCTCCAAGTGTGCT T A PIP5K1C Ensembl:ENSG00000186111 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1161907777 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98930,RMVar_hsa_circ_87171,RMVar_hsa_circ_191395,RMVar_hsa_circ_191398 23790 RMVar_ID_23790 Human_SNP_ID_656184179 A-to-I Human chr19 - 3690431 3690431 3690431 TCACCCAGGCTAGAGTTCAGTGACACGATTGTAGCTCACCGCAGCCTCGACCTCCTGGGTTCAAA TCACCCAGGCTAGAGTTCAGTGACACGATTGTGGCTCACCGCAGCCTCGACCTCCTGGGTTCAAA T C PIP5K1C Ensembl:ENSG00000186111 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs906569998 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13440661 RMVar_hsa_circ_98930,RMVar_hsa_circ_87171,RMVar_hsa_circ_191395,RMVar_hsa_circ_191398 23791 RMVar_ID_23791 Human_SNP_ID_656203107 A-to-I Human chr19 - 3747123 3747123 3747123 CCGGGAGGCGGAGGTTGCAGCAAGCTGAGATCACACCACTGTACTCCAGCCTGGGTGACATGAGA CCGGGAGGCGGAGGTTGCAGCAAGCTGAGATCGCACCACTGTACTCCAGCCTGGGTGACATGAGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432924816 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25410090 23792 RMVar_ID_23792 Human_SNP_ID_656203108 A-to-I Human chr19 - 3747123 3747123 3747123 CCGGGAGGCGGAGGTTGCAGCAAGCTGAGATCACACCACTGTACTCCAGCCTGGGTGACATGAGA CCGGGAGGCGGAGGTTGCAGCAAGCTGAGATCCCACCACTGTACTCCAGCCTGGGTGACATGAGA T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432924816 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25410090 23793 RMVar_ID_23793 Human_SNP_ID_656206169 A-to-I Human chr19 - 3754759 3754759 3754759 ATGAGACTGAGGCAGGAGAATCGTTTGAACCCAGGAAGCGGAGGTTGCAGTGAGCTGAGATCACA ATGAGACTGAGGCAGGAGAATCGTTTGAACCCCGGAAGCGGAGGTTGCAGTGAGCTGAGATCACA T G APBA3,AC005954.1 Ensembl:ENSG00000011132,Ensembl:ENSG00000267138 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1321326157 Functional Loss SNV dbSNP153 33..33 33 - - - 23794 RMVar_ID_23794 Human_SNP_ID_656206171 A-to-I Human chr19 - 3754763 3754763 3754763 ACTCATGAGACTGAGGCAGGAGAATCGTTTGAACCCAGGAAGCGGAGGTTGCAGTGAGCTGAGAT ACTCATGAGACTGAGGCAGGAGAATCGTTTGAGCCCAGGAAGCGGAGGTTGCAGTGAGCTGAGAT T C APBA3,AC005954.1 Ensembl:ENSG00000011132,Ensembl:ENSG00000267138 Protein coding,lincRNA intron,intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs531840194 Functional Loss SNV dbSNP153 33..33 33 - - - 23795 RMVar_ID_23795 Human_SNP_ID_656206172 A-to-I Human chr19 - 3754764 3754764 3754764 TACTCATGAGACTGAGGCAGGAGAATCGTTTGAACCCAGGAAGCGGAGGTTGCAGTGAGCTGAGA TACTCATGAGACTGAGGCAGGAGAATCGTTTGTACCCAGGAAGCGGAGGTTGCAGTGAGCTGAGA T A APBA3,AC005954.1 Ensembl:ENSG00000011132,Ensembl:ENSG00000267138 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1392641750 Functional Loss SNV dbSNP153 33..33 33 - - - 23796 RMVar_ID_23796 Human_SNP_ID_656206208 A-to-I Human chr19 - 3754870 3754870 3754870 TTGAGGTCGGGAGTTTGAGACCAGCCTGGCCAACGTGGCGAAACCCCGTCTCTACTAAAAATACA TTGAGGTCGGGAGTTTGAGACCAGCCTGGCCATCGTGGCGAAACCCCGTCTCTACTAAAAATACA T A APBA3,AC005954.1 Ensembl:ENSG00000011132,Ensembl:ENSG00000267138 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1568393973 Functional Loss SNV dbSNP153 33..33 33 - - - 23797 RMVar_ID_23797 Human_SNP_ID_656206989 A-to-I Human chr19 - 3757189 3757189 3757189 GAGGCTGAGGTGGGAGGATCACTTGAGGCTGCAGTGAGCTAAGATTGTGCCACTGCACTCCAGCC GAGGCTGAGGTGGGAGGATCACTTGAGGCTGCGGTGAGCTAAGATTGTGCCACTGCACTCCAGCC T C APBA3 Ensembl:ENSG00000011132 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1039888171 Functional Loss SNV dbSNP153 33..33 33 - - - 23798 RMVar_ID_23798 Human_SNP_ID_656207012 A-to-I Human chr19 - 3757262 3757262 3757262 TCTCCACAAAAATAAAATCCCCCCCCAAAATTAGCCAGGCACGTGGCATGGGTCTATAATCCCAG TCTCCACAAAAATAAAATCCCCCCCCAAAATTGGCCAGGCACGTGGCATGGGTCTATAATCCCAG T C APBA3 Ensembl:ENSG00000011132 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1009230633 Functional Loss SNV dbSNP153 33..33 33 - - - 23799 RMVar_ID_23799 Human_SNP_ID_656207044 A-to-I Human chr19 - 3757373 3757373 3757373 GCCGGGAAGGGTGGCTCACATCTGTAATCCCAACACTTTGAAAGGCTGATGTGGGAGGATCGCTT GCCGGGAAGGGTGGCTCACATCTGTAATCCCATCACTTTGAAAGGCTGATGTGGGAGGATCGCTT T A APBA3 Ensembl:ENSG00000011132 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs745977882 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8485674 23800 RMVar_ID_23800 Human_SNP_ID_656207257 A-to-I Human chr19 - 3758086 3758086 3758086 TACTAAACATACAAAAATTAGCCGGGCATGGTAGTGCACGCCTGTAATCCCAGCTACTCAGGAGG TACTAAACATACAAAAATTAGCCGGGCATGGTCGTGCACGCCTGTAATCCCAGCTACTCAGGAGG T G APBA3 Ensembl:ENSG00000011132 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs769710805 Functional Loss SNV dbSNP153 33..33 33 - - - 23801 RMVar_ID_23801 Human_SNP_ID_656207308 A-to-I Human chr19 - 3758198 3758198 3758198 TGGGCGCGGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCCAAGGTGGGCAGATCACTAGG TGGGCGCGGTGGCTCACGCCTATAATCCCAGCGCTTTGGGAGGCCAAGGTGGGCAGATCACTAGG T C APBA3 Ensembl:ENSG00000011132 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1185984451 Functional Loss SNV dbSNP153 33..33 33 - - - 23802 RMVar_ID_23802 Human_SNP_ID_656207311 A-to-I Human chr19 - 3758207 3758207 3758207 TGCATAAGCTGGGCGCGGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCCAAGGTGGGCAG TGCATAAGCTGGGCGCGGTGGCTCACGCCTATGATCCCAGCACTTTGGGAGGCCAAGGTGGGCAG T C APBA3 Ensembl:ENSG00000011132 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1363933673 Functional Loss SNV dbSNP153 33..33 33 - - - 23803 RMVar_ID_23803 Human_SNP_ID_656207365 A-to-I Human chr19 - 3758351 3758351 3758351 AGGAGGTTGAGGCGGGAGAAGTTCTTGAGCCCAGGAGGTCGAGACTGCGGTGAGCTGAGATCACC AGGAGGTTGAGGCGGGAGAAGTTCTTGAGCCCGGGAGGTCGAGACTGCGGTGAGCTGAGATCACC T C APBA3 Ensembl:ENSG00000011132 Protein coding intron GSE38233;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,32596459 RNA-Seq:(High) rs1038235144 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13444037,Human_RBP_ID_17567873,Human_RBP_ID_23177059 23804 RMVar_ID_23804 Human_SNP_ID_656207367 A-to-I Human chr19 - 3758356 3758356 3758356 TACTCAGGAGGTTGAGGCGGGAGAAGTTCTTGAGCCCAGGAGGTCGAGACTGCGGTGAGCTGAGA TACTCAGGAGGTTGAGGCGGGAGAAGTTCTTGTGCCCAGGAGGTCGAGACTGCGGTGAGCTGAGA T A APBA3 Ensembl:ENSG00000011132 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs921677481 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13444038,Human_RBP_ID_17567873,Human_RBP_ID_23177059 23805 RMVar_ID_23805 Human_SNP_ID_656207585 A-to-I Human chr19 - 3759029 3759029 3759029 TGGGTAGAGATGGGGTTTCACCATGTTGCCCAAGCTGGTTTCAAACTCCTGAGCTCAAGCGATCT TGGGTAGAGATGGGGTTTCACCATGTTGCCCATGCTGGTTTCAAACTCCTGAGCTCAAGCGATCT T A APBA3 Ensembl:ENSG00000011132 Protein coding intron GSE38233;GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,32596459 RNA-Seq:(High) rs930794919 Functional Loss SNV dbSNP153 33..33 33 - - - 23806 RMVar_ID_23806 Human_SNP_ID_656207628 A-to-I Human chr19 - 3759207 3759207 3759207 GGGCTTCTTTACTTTTTTTGATGACTTCTGTTATCCAGGCTGGAGTGCAGTGGCTTGATCTCAGC GGGCTTCTTTACTTTTTTTGATGACTTCTGTTGTCCAGGCTGGAGTGCAGTGGCTTGATCTCAGC T C APBA3 Ensembl:ENSG00000011132 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs750682733 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22476391 23807 RMVar_ID_23807 Human_SNP_ID_656268983 A-to-I Human chr19 - 3958505 3958505 3958505 CGCGAGCCCCATCGTCGCGCCTGTGGACGCCTAGGCAAGAGCGGCCCTCTGCAGCCAAGAGAAAT CGCGAGCCCCATCGTCGCGCCTGTGGACGCCTGGGCAAGAGCGGCCCTCTGCAGCCAAGAGAAAT T C DAPK3 Ensembl:ENSG00000167657 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1257988533 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_521372,Human_RBP_ID_4568047,Human_RBP_ID_5144940,Human_RBP_ID_13451790,Human_RBP_ID_27467810 RMVar_hsa_circ_106011,RMVar_hsa_circ_191421,RMVar_hsa_circ_76453,RMVar_hsa_circ_191420 23808 RMVar_ID_23808 Human_SNP_ID_656270572 A-to-I Human chr19 - 3961983 3961983 3961983 GTGGCAGCGGGTGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATGGCATGAACCCA GTGGCAGCGGGTGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCATGAACCCA T C DAPK3 Ensembl:ENSG00000167657 Protein coding intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs866817689 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16480,RMVar_hsa_circ_106011,RMVar_hsa_circ_191421,RMVar_hsa_circ_76453,RMVar_hsa_circ_191420 23809 RMVar_ID_23809 Human_SNP_ID_656270607 A-to-I Human chr19 - 3962129 3962129 3962129 AGATGGGCCGGGTGCGATGGCTCACGCCTGTAATCTCAGCACTTTGGGAGGCTGAGGAGGGCAGA AGATGGGCCGGGTGCGATGGCTCACGCCTGTACTCTCAGCACTTTGGGAGGCTGAGGAGGGCAGA T G DAPK3 Ensembl:ENSG00000167657 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs534612569 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16480,RMVar_hsa_circ_106011,RMVar_hsa_circ_191421,RMVar_hsa_circ_76453,RMVar_hsa_circ_191420 23810 RMVar_ID_23810 Human_SNP_ID_656270761 A-to-I Human chr19 - 3962694 3962694 3962694 AGGCTTACTGCAACCTCTGCCTCCCGGGTTCAAGTGATTCCCATGCCTCAGCCTCCCAAGTAGCT AGGCTTACTGCAACCTCTGCCTCCCGGGTTCAGGTGATTCCCATGCCTCAGCCTCCCAAGTAGCT T C DAPK3 Ensembl:ENSG00000167657 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs927522063 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16480,RMVar_hsa_circ_106011,RMVar_hsa_circ_191421,RMVar_hsa_circ_76453,RMVar_hsa_circ_191420 23811 RMVar_ID_23811 Human_SNP_ID_656270856 A-to-I Human chr19 - 3962919 3962919 3962919 TTTTGTATTTTTAGAAGAGACGGGGTTTCACCATGTTGATCAAGGCTGGTTTTGAACTCCTGACC TTTTGTATTTTTAGAAGAGACGGGGTTTCACCGTGTTGATCAAGGCTGGTTTTGAACTCCTGACC T C DAPK3 Ensembl:ENSG00000167657 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs528180601 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13451929 RMVar_hsa_circ_16480,RMVar_hsa_circ_106011,RMVar_hsa_circ_191421,RMVar_hsa_circ_76453,RMVar_hsa_circ_191420 23812 RMVar_ID_23812 Human_SNP_ID_656271933 A-to-I Human chr19 - 3965571 3965571 3965571 CTACGTTGCCCAGGCTGGAGTACAGTGGCACAATCTCAGTTCACTGCAACCTCTGCCTCCCAGGT CTACGTTGCCCAGGCTGGAGTACAGTGGCACAGTCTCAGTTCACTGCAACCTCTGCCTCCCAGGT T C DAPK3 Ensembl:ENSG00000167657 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs760425676 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_191422,RMVar_hsa_circ_77341 23813 RMVar_ID_23813 Human_SNP_ID_656271994 A-to-I Human chr19 - 3965776 3965776 3965776 CCTGTAGTCCCAGCTGCTTGAGAGGCTGAGGCAGGAGGATTGCCCGAGCCCAGGAGGTCAAGGCT CCTGTAGTCCCAGCTGCTTGAGAGGCTGAGGCGGGAGGATTGCCCGAGCCCAGGAGGTCAAGGCT T C DAPK3 Ensembl:ENSG00000167657 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1363221944 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_191422,RMVar_hsa_circ_77341 23814 RMVar_ID_23814 Human_SNP_ID_656272000 A-to-I Human chr19 - 3965803 3965803 3965803 AAAATTAATTGGGTGTGGTGGTATGTGCCTGTAGTCCCAGCTGCTTGAGAGGCTGAGGCAGGAGG AAAATTAATTGGGTGTGGTGGTATGTGCCTGTGGTCCCAGCTGCTTGAGAGGCTGAGGCAGGAGG T C DAPK3 Ensembl:ENSG00000167657 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917875164 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_191422,RMVar_hsa_circ_77341 23815 RMVar_ID_23815 Human_SNP_ID_656274165 A-to-I Human chr19 - 3972405 3972405 3972405 TGAGGCAGGAGAATCGCTTGAACCCAGGAGGCAGAGATTGCAGTGAGCCCAGATCTCACCACTGC TGAGGCAGGAGAATCGCTTGAACCCAGGAGGCGGAGATTGCAGTGAGCCCAGATCTCACCACTGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1255822173 Functional Loss SNV dbSNP153 33..33 33 - - - 23816 RMVar_ID_23816 Human_SNP_ID_656302019 A-to-I Human chr19 - 4046946 4046946 4046946 ACAACCGGCGGGACCCCCAGGGACCACCCCTCAGGGCGCCCCCCCACCCCCGCCCGGTCCACCTA ACAACCGGCGGGACCCCCAGGGACCACCCCTCTGGGCGCCCCCCCACCCCCGCCCGGTCCACCTA T A ZBTB7A Ensembl:ENSG00000178951 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1172849011 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_111324,Human_miRNA_ID_120327,Human_miRNA_ID_124142,Human_miRNA_ID_864938,Human_miRNA_ID_1004287,Human_miRNA_ID_1267585,Human_miRNA_ID_1973801,Human_miRNA_ID_1975979,Human_miRNA_ID_2153841,Human_miRNA_ID_2613769,Human_miRNA_ID_2801717,Human_miRNA_ID_3009849 RMVar_hsa_circ_191491,RMVar_hsa_circ_123623 23817 RMVar_ID_23817 Human_SNP_ID_656302020 A-to-I Human chr19 - 4046946 4046946 4046946 ACAACCGGCGGGACCCCCAGGGACCACCCCTCAGGGCGCCCCCCCACCCCCGCCCGGTCCACCTA ACAACCGGCGGGACCCCCAGGGACCACCCCTCCGGGCGCCCCCCCACCCCCGCCCGGTCCACCTA T G ZBTB7A Ensembl:ENSG00000178951 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1172849011 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_111324,Human_miRNA_ID_120327,Human_miRNA_ID_124142,Human_miRNA_ID_864938,Human_miRNA_ID_1004287,Human_miRNA_ID_1267585,Human_miRNA_ID_1973801,Human_miRNA_ID_1975979,Human_miRNA_ID_2153841,Human_miRNA_ID_2613769,Human_miRNA_ID_2801717,Human_miRNA_ID_3009849 RMVar_hsa_circ_191491,RMVar_hsa_circ_123623 23818 RMVar_ID_23818 Human_SNP_ID_656302025 A-to-I Human chr19 - 4046960 4046960 4046960 CCTTCACGGCACTTACAACCGGCGGGACCCCCAGGGACCACCCCTCAGGGCGCCCCCCCACCCCC CCTTCACGGCACTTACAACCGGCGGGACCCCCCGGGACCACCCCTCAGGGCGCCCCCCCACCCCC T G ZBTB7A Ensembl:ENSG00000178951 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs979549370 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1973801,Human_miRNA_ID_1975979,Human_miRNA_ID_2153841,Human_miRNA_ID_2801717,Human_miRNA_ID_3009849 RMVar_hsa_circ_191491,RMVar_hsa_circ_123623 23819 RMVar_ID_23819 Human_SNP_ID_656312758 A-to-I Human chr19 - 4079193 4079193 4079193 AAAATTAGCCGGGCATGGTGGTGGGCGCCTGTAGTCCCAGCTACTCTGGAGGCTGAGACACGAGA AAAATTAGCCGGGCATGGTGGTGGGCGCCTGTGGTCCCAGCTACTCTGGAGGCTGAGACACGAGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417674400 Functional Loss SNV dbSNP153 33..33 33 - - - 23820 RMVar_ID_23820 Human_SNP_ID_656314496 A-to-I Human chr19 - 4085079 4085079 4085079 ATGATCTGACCGCCTTGGCCTCCCAAAGTGCTAGGATGACAGGTGTGAGCCACCACGCTGGGTGG ATGATCTGACCGCCTTGGCCTCCCAAAGTGCTGGGATGACAGGTGTGAGCCACCACGCTGGGTGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1333293300 Functional Loss SNV dbSNP153 33..33 33 - - - 23821 RMVar_ID_23821 Human_SNP_ID_656316613 A-to-I Human chr19 - 4091628 4091628 4091628 AAAATTAAGGCCAGTTGCGGTGGCTCACACCTATAATCCCAGCACTTCGGGAAGCTGAGGCAGGA AAAATTAAGGCCAGTTGCGGTGGCTCACACCTGTAATCCCAGCACTTCGGGAAGCTGAGGCAGGA T C MAP2K2 Ensembl:ENSG00000126934 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1196944260 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25418124 RMVar_hsa_circ_96157,RMVar_hsa_circ_191493 23822 RMVar_ID_23822 Human_SNP_ID_656316639 A-to-I Human chr19 - 4091734 4091734 4091734 TGAGGCGGGAGAATTGCTTGAACCTGGGAGGCAGAGGTTACAGTGAGCTGAGATCATACCACTGC TGAGGCGGGAGAATTGCTTGAACCTGGGAGGCTGAGGTTACAGTGAGCTGAGATCATACCACTGC T A MAP2K2 Ensembl:ENSG00000126934 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1000398062 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96157,RMVar_hsa_circ_191493 23823 RMVar_ID_23823 Human_SNP_ID_656316987 A-to-I Human chr19 - 4093155 4093155 4093155 GGAGTGCAGTGGTACGATCTCGGCTCACTGCAACCTCCGCCTCCCAGGTTCAGGGAATTCTCCTG GGAGTGCAGTGGTACGATCTCGGCTCACTGCAGCCTCCGCCTCCCAGGTTCAGGGAATTCTCCTG T C MAP2K2 Ensembl:ENSG00000126934 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1314367836 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96157,RMVar_hsa_circ_191493 23824 RMVar_ID_23824 Human_SNP_ID_656317049 A-to-I Human chr19 - 4093363 4093363 4093363 AGATACAGCCTTGCTCTGTCCCCCAGGCTGGAATGCAGTGGTGCGATTGTAGCTCACTGTAGCCC AGATACAGCCTTGCTCTGTCCCCCAGGCTGGAGTGCAGTGGTGCGATTGTAGCTCACTGTAGCCC T C MAP2K2 Ensembl:ENSG00000126934 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1231397334 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13458896 RMVar_hsa_circ_96157,RMVar_hsa_circ_191493 23825 RMVar_ID_23825 Human_SNP_ID_656317070 A-to-I Human chr19 - 4093425 4093425 4093425 CAGCCTCCCAAAGTGCAGAGATTACAGATGTGAGCCACCGCACCTGGTCAAAAAAATTTTTGAGA CAGCCTCCCAAAGTGCAGAGATTACAGATGTGCGCCACCGCACCTGGTCAAAAAAATTTTTGAGA T G MAP2K2 Ensembl:ENSG00000126934 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027842258 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96157,RMVar_hsa_circ_191493 23826 RMVar_ID_23826 Human_SNP_ID_656320846 A-to-I Human chr19 - 4104007 4104007 4104007 CGCCTGCCTCAGCCTCCCAAAGTCCTGGCATTACAGGCGTGAGTCACCGCTCCCAGCCCATGTCC CGCCTGCCTCAGCCTCCCAAAGTCCTGGCATTGCAGGCGTGAGTCACCGCTCCCAGCCCATGTCC T C MAP2K2 Ensembl:ENSG00000126934 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1297060154 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92829,RMVar_hsa_circ_344908,RMVar_hsa_circ_34095,RMVar_hsa_circ_44816,RMVar_hsa_circ_191496 23827 RMVar_ID_23827 Human_SNP_ID_656320866 A-to-I Human chr19 - 4104116 4104115 4104116 AGATTACAGGCATCCACCACCACGCCCAGCTAATTTTTTTTATTTTTAGTGGAGATGGGGTTTTA AGATTACAGGCATCCACCACCACGCCCAGCTA_TTTTTTTTATTTTTAGTGGAGATGGGGTTTTA AT A MAP2K2 Ensembl:ENSG00000126934 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1267336355 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_92829,RMVar_hsa_circ_344908,RMVar_hsa_circ_34095,RMVar_hsa_circ_44816,RMVar_hsa_circ_191496 23828 RMVar_ID_23828 Human_SNP_ID_656320871 A-to-I Human chr19 - 4104137 4104137 4104137 CCTCAGCCTCCCGAGTAGCTGAGATTACAGGCATCCACCACCACGCCCAGCTAATTTTTTTTATT CCTCAGCCTCCCGAGTAGCTGAGATTACAGGCGTCCACCACCACGCCCAGCTAATTTTTTTTATT T C MAP2K2 Ensembl:ENSG00000126934 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1185635354 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92829,RMVar_hsa_circ_344908,RMVar_hsa_circ_34095,RMVar_hsa_circ_44816,RMVar_hsa_circ_191496 23829 RMVar_ID_23829 Human_SNP_ID_656320875 A-to-I Human chr19 - 4104148 4104148 4104148 TGATCTTCCTGCCTCAGCCTCCCGAGTAGCTGAGATTACAGGCATCCACCACCACGCCCAGCTAA TGATCTTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCATCCACCACCACGCCCAGCTAA T C MAP2K2 Ensembl:ENSG00000126934 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs962263568 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92829,RMVar_hsa_circ_344908,RMVar_hsa_circ_34095,RMVar_hsa_circ_44816,RMVar_hsa_circ_191496 23830 RMVar_ID_23830 Human_SNP_ID_656320884 A-to-I Human chr19 - 4104182 4104182 4104182 CGACTCACAGCAACCTCTGCCTCCCAGGTTCAAGTGATCTTCCTGCCTCAGCCTCCCGAGTAGCT CGACTCACAGCAACCTCTGCCTCCCAGGTTCAGGTGATCTTCCTGCCTCAGCCTCCCGAGTAGCT T C MAP2K2 Ensembl:ENSG00000126934 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs986172556 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92829,RMVar_hsa_circ_344908,RMVar_hsa_circ_34095,RMVar_hsa_circ_44816,RMVar_hsa_circ_191496 23831 RMVar_ID_23831 Human_SNP_ID_656320886 A-to-I Human chr19 - 4104189 4104189 4104189 ACGATCTCGACTCACAGCAACCTCTGCCTCCCAGGTTCAAGTGATCTTCCTGCCTCAGCCTCCCG ACGATCTCGACTCACAGCAACCTCTGCCTCCCGGGTTCAAGTGATCTTCCTGCCTCAGCCTCCCG T C MAP2K2 Ensembl:ENSG00000126934 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1231687667 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92829,RMVar_hsa_circ_344908,RMVar_hsa_circ_34095,RMVar_hsa_circ_44816,RMVar_hsa_circ_191496 23832 RMVar_ID_23832 Human_SNP_ID_656320998 A-to-I Human chr19 - 4104477 4104477 4104477 GTGATCTCGGCTCACTGCAACCTTGACCTCCCAGGTTCAAGGGATCCTCCCACCTCAGCCTTCTG GTGATCTCGGCTCACTGCAACCTTGACCTCCCTGGTTCAAGGGATCCTCCCACCTCAGCCTTCTG T A MAP2K2 Ensembl:ENSG00000126934 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs924414593 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92829,RMVar_hsa_circ_344908,RMVar_hsa_circ_34095,RMVar_hsa_circ_44816,RMVar_hsa_circ_191496 23833 RMVar_ID_23833 Human_SNP_ID_656321014 A-to-I Human chr19 - 4104547 4104545 4104547 TGGTCTCTTTCTGGTTTTTGTTTTTTTGAGACAGGGTCTTGCTCTGTCACCCAGGCTGGAGTGCA TGGTCTCTTTCTGGTTTTTGTTTTTTTGAGAC__GGTCTTGCTCTGTCACCCAGGCTGGAGTGCA CCT C MAP2K2 Ensembl:ENSG00000126934 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1298457275 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_3572234 RMVar_hsa_circ_92829,RMVar_hsa_circ_344908,RMVar_hsa_circ_34095,RMVar_hsa_circ_44816,RMVar_hsa_circ_191496 23834 RMVar_ID_23834 Human_SNP_ID_656321015 A-to-I Human chr19 - 4104547 4104547 4104547 TGGTCTCTTTCTGGTTTTTGTTTTTTTGAGACAGGGTCTTGCTCTGTCACCCAGGCTGGAGTGCA TGGTCTCTTTCTGGTTTTTGTTTTTTTGAGACTGGGTCTTGCTCTGTCACCCAGGCTGGAGTGCA T A MAP2K2 Ensembl:ENSG00000126934 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1433034708 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3572234 RMVar_hsa_circ_92829,RMVar_hsa_circ_344908,RMVar_hsa_circ_34095,RMVar_hsa_circ_44816,RMVar_hsa_circ_191496 23835 RMVar_ID_23835 Human_SNP_ID_656321054 A-to-I Human chr19 - 4104670 4104669 4104671 ACAAACATTGATTGCGGCCCCAGGAGAAACGAAGACGGAAGGAGCTGTGCTGGGGAGCAGGGGTT ACAAACATTGATTGCGGCCCCAGGAGAAACG__GACGGAAGGAGCTGTGCTGGGGAGCAGGGGTT CTT C MAP2K2 Ensembl:ENSG00000126934 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1480575971 Functional Loss DEL dbSNP153 32..33 33 - - - Human_Splice_Rec_1939011 RMVar_hsa_circ_92829,RMVar_hsa_circ_344908,RMVar_hsa_circ_34095,RMVar_hsa_circ_44816,RMVar_hsa_circ_191496 23836 RMVar_ID_23836 Human_SNP_ID_656321304 A-to-I Human chr19 - 4105304 4105304 4105304 AGATGGTGCCACTGCACCCCCGCCTGGGCAACAGAGCGAGACTCCGCCTCAGGAAAAAAAAAAAA AGATGGTGCCACTGCACCCCCGCCTGGGCAACGGAGCGAGACTCCGCCTCAGGAAAAAAAAAAAA T C MAP2K2 Ensembl:ENSG00000126934 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1175264439 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92829,RMVar_hsa_circ_344908,RMVar_hsa_circ_34095,RMVar_hsa_circ_44816,RMVar_hsa_circ_191496 23837 RMVar_ID_23837 Human_SNP_ID_656321305 A-to-I Human chr19 - 4105307 4105307 4105307 CCGAGATGGTGCCACTGCACCCCCGCCTGGGCAACAGAGCGAGACTCCGCCTCAGGAAAAAAAAA CCGAGATGGTGCCACTGCACCCCCGCCTGGGCGACAGAGCGAGACTCCGCCTCAGGAAAAAAAAA T C MAP2K2 Ensembl:ENSG00000126934 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1480524927 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92829,RMVar_hsa_circ_344908,RMVar_hsa_circ_34095,RMVar_hsa_circ_44816,RMVar_hsa_circ_191496 23838 RMVar_ID_23838 Human_SNP_ID_656321456 A-to-I Human chr19 - 4105728 4105728 4105728 TGGAGGCTGCAGTGAGCCAAGATCACAGCACTATGCTGCAGTCTGGGCGACCCCTGCCTGAAAGA TGGAGGCTGCAGTGAGCCAAGATCACAGCACTGTGCTGCAGTCTGGGCGACCCCTGCCTGAAAGA T C MAP2K2 Ensembl:ENSG00000126934 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs952582326 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92829,RMVar_hsa_circ_344908,RMVar_hsa_circ_34095,RMVar_hsa_circ_44816,RMVar_hsa_circ_191496 23839 RMVar_ID_23839 Human_SNP_ID_656321473 A-to-I Human chr19 - 4105802 4105802 4105802 CAGGACATGGTGGCGCGCCTGTACTCCCAGCTACTTGGGAAGCTGAGGTGGGAGGACTGCCTGAA CAGGACATGGTGGCGCGCCTGTACTCCCAGCTGCTTGGGAAGCTGAGGTGGGAGGACTGCCTGAA T C MAP2K2 Ensembl:ENSG00000126934 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1225555070 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92829,RMVar_hsa_circ_344908,RMVar_hsa_circ_34095,RMVar_hsa_circ_44816,RMVar_hsa_circ_191496 23840 RMVar_ID_23840 Human_SNP_ID_656321475 A-to-I Human chr19 - 4105806 4105806 4105806 TTAGCAGGACATGGTGGCGCGCCTGTACTCCCAGCTACTTGGGAAGCTGAGGTGGGAGGACTGCC TTAGCAGGACATGGTGGCGCGCCTGTACTCCCTGCTACTTGGGAAGCTGAGGTGGGAGGACTGCC T A MAP2K2 Ensembl:ENSG00000126934 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs923395225 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92829,RMVar_hsa_circ_344908,RMVar_hsa_circ_34095,RMVar_hsa_circ_44816,RMVar_hsa_circ_191496 23841 RMVar_ID_23841 Human_SNP_ID_656321492 A-to-I Human chr19 - 4105865 4105865 4105865 TCAGCCAGGACTTCGAGAGCAGCCTGGGCAACATGAGGAACCCCCGTCTCTACAAAAAATTAGCA TCAGCCAGGACTTCGAGAGCAGCCTGGGCAACGTGAGGAACCCCCGTCTCTACAAAAAATTAGCA T C MAP2K2 Ensembl:ENSG00000126934 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs780241828 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17568323 RMVar_hsa_circ_92829,RMVar_hsa_circ_344908,RMVar_hsa_circ_34095,RMVar_hsa_circ_44816,RMVar_hsa_circ_191496 23842 RMVar_ID_23842 Human_SNP_ID_656321570 A-to-I Human chr19 - 4106234 4106234 4106234 CAGCTAATTTATTTGCTTATTTGTGTAGAGATAGGGTCTCTCCATATTGCCCAGACTGGTCTTGA CAGCTAATTTATTTGCTTATTTGTGTAGAGATGGGGTCTCTCCATATTGCCCAGACTGGTCTTGA T C MAP2K2 Ensembl:ENSG00000126934 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs571011396 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17568325 RMVar_hsa_circ_92829,RMVar_hsa_circ_344908,RMVar_hsa_circ_34095,RMVar_hsa_circ_44816,RMVar_hsa_circ_191496 23843 RMVar_ID_23843 Human_SNP_ID_656321664 A-to-I Human chr19 - 4106626 4106626 4106626 CAAGGCAGGCGGATCACGAGGTCAAGAGTTCAAGACCATCCTGGCCAACATGGTGAAACCCCATC CAAGGCAGGCGGATCACGAGGTCAAGAGTTCAGGACCATCCTGGCCAACATGGTGAAACCCCATC T C MAP2K2 Ensembl:ENSG00000126934 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1202602961 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92829,RMVar_hsa_circ_344908,RMVar_hsa_circ_34095,RMVar_hsa_circ_44816,RMVar_hsa_circ_191496 23844 RMVar_ID_23844 Human_SNP_ID_656321784 A-to-I Human chr19 - 4107178 4107176 4107178 TTTCCCAGGCTAATCTTGAACTCCTGGGCTCAAACGATTCTCCCGCCTCAGCCTCCCAAAGTGCT TTTCCCAGGCTAATCTTGAACTCCTGGGCTCA__CGATTCTCCCGCCTCAGCCTCCCAAAGTGCT GTT G MAP2K2 Ensembl:ENSG00000126934 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1302137782 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_25418230 RMVar_hsa_circ_92829,RMVar_hsa_circ_344908,RMVar_hsa_circ_34095,RMVar_hsa_circ_44816,RMVar_hsa_circ_191496 23845 RMVar_ID_23845 Human_SNP_ID_656321784 A-to-I Human chr19 - 4107177 4107176 4107178 TTCCCAGGCTAATCTTGAACTCCTGGGCTCAAACGATTCTCCCGCCTCAGCCTCCCAAAGTGCTG TTCCCAGGCTAATCTTGAACTCCTGGGCTCA__CGATTCTCCCGCCTCAGCCTCCCAAAGTGCTG GTT G MAP2K2 Ensembl:ENSG00000126934 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1302137782 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_25418230 RMVar_hsa_circ_92829,RMVar_hsa_circ_344908,RMVar_hsa_circ_34095,RMVar_hsa_circ_44816,RMVar_hsa_circ_191496 23846 RMVar_ID_23846 Human_SNP_ID_656321785 A-to-I Human chr19 - 4107177 4107177 4107177 TTCCCAGGCTAATCTTGAACTCCTGGGCTCAAACGATTCTCCCGCCTCAGCCTCCCAAAGTGCTG TTCCCAGGCTAATCTTGAACTCCTGGGCTCAAGCGATTCTCCCGCCTCAGCCTCCCAAAGTGCTG T C MAP2K2 Ensembl:ENSG00000126934 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1568257845 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25418230 RMVar_hsa_circ_92829,RMVar_hsa_circ_344908,RMVar_hsa_circ_34095,RMVar_hsa_circ_44816,RMVar_hsa_circ_191496 23847 RMVar_ID_23847 Human_SNP_ID_656321823 A-to-I Human chr19 - 4107265 4107265 4107265 CTGCCTCTGCCTCCCAAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCCCGGCAAGTTTTTTT CTGCCTCTGCCTCCCAAAAGTGCTGGGATTACCGGCGTGAGCCACCGCGCCCGGCAAGTTTTTTT T G MAP2K2 Ensembl:ENSG00000126934 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1349362061 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92829,RMVar_hsa_circ_344908,RMVar_hsa_circ_34095,RMVar_hsa_circ_44816,RMVar_hsa_circ_191496 23848 RMVar_ID_23848 Human_SNP_ID_656321855 A-to-I Human chr19 - 4107357 4107350 4107357 ACCACAGCCGGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCGCTGTGTTAGCCAGGATGG ACCACAGCCGGCTAATTTTTTGTATTTTTAGT_______GGGTTTCGCTGTGTTAGCCAGGATGG CCGTCTCT C MAP2K2 Ensembl:ENSG00000126934 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1469371058 Functional Loss DEL dbSNP153 33..39 33 - - - RMVar_hsa_circ_92829,RMVar_hsa_circ_344908,RMVar_hsa_circ_34095,RMVar_hsa_circ_44816,RMVar_hsa_circ_191496 23849 RMVar_ID_23849 Human_SNP_ID_656322000 A-to-I Human chr19 - 4107685 4107685 4107685 GGGGGGTAGGGGGTACAAGGTCTCTCTCTGTCACCCAGGTTGGAGTGCAGTGGCATGATCCTAGC GGGGGGTAGGGGGTACAAGGTCTCTCTCTGTCGCCCAGGTTGGAGTGCAGTGGCATGATCCTAGC T C MAP2K2 Ensembl:ENSG00000126934 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs550216390 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23178438 RMVar_hsa_circ_92829,RMVar_hsa_circ_344908,RMVar_hsa_circ_34095,RMVar_hsa_circ_44816,RMVar_hsa_circ_191496 23850 RMVar_ID_23850 Human_SNP_ID_656322194 A-to-I Human chr19 - 4108326 4108326 4108326 TGAGGCAGGGGAATGGCGTGAACCCTGGAGGCAGAGCTTTCAGTGAGCTGAGATCGTGCCACTGC TGAGGCAGGGGAATGGCGTGAACCCTGGAGGCGGAGCTTTCAGTGAGCTGAGATCGTGCCACTGC T C MAP2K2 Ensembl:ENSG00000126934 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1440543809 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92829,RMVar_hsa_circ_344908,RMVar_hsa_circ_34095,RMVar_hsa_circ_44816,RMVar_hsa_circ_191496 23851 RMVar_ID_23851 Human_SNP_ID_656322196 A-to-I Human chr19 - 4108337 4108337 4108337 ACTTGGGAGGCTGAGGCAGGGGAATGGCGTGAACCCTGGAGGCAGAGCTTTCAGTGAGCTGAGAT ACTTGGGAGGCTGAGGCAGGGGAATGGCGTGACCCCTGGAGGCAGAGCTTTCAGTGAGCTGAGAT T G MAP2K2 Ensembl:ENSG00000126934 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs931090735 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92829,RMVar_hsa_circ_344908,RMVar_hsa_circ_34095,RMVar_hsa_circ_44816,RMVar_hsa_circ_191496 23852 RMVar_ID_23852 Human_SNP_ID_656322562 A-to-I Human chr19 - 4109517 4109517 4109517 GGAAGATCACTTGAGCCCAGGAGGTTGAGGCTACAGTGAGCTTTGGTCACGCCACTGCACTCCAG GGAAGATCACTTGAGCCCAGGAGGTTGAGGCTGCAGTGAGCTTTGGTCACGCCACTGCACTCCAG T C MAP2K2 Ensembl:ENSG00000126934 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1227745008 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92829,RMVar_hsa_circ_344908,RMVar_hsa_circ_34095,RMVar_hsa_circ_44816,RMVar_hsa_circ_191496 23853 RMVar_ID_23853 Human_SNP_ID_656322743 A-to-I Human chr19 - 4110241 4110241 4110241 ATCTAGTAGTGGCACAATCTCGGCTCACTGCAACCTCCACCTCCCAGATTCAAGTGATACTTCTG ATCTAGTAGTGGCACAATCTCGGCTCACTGCAGCCTCCACCTCCCAGATTCAAGTGATACTTCTG T C MAP2K2 Ensembl:ENSG00000126934 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025625139 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92829,RMVar_hsa_circ_344908,RMVar_hsa_circ_34095,RMVar_hsa_circ_44816,RMVar_hsa_circ_191496 23854 RMVar_ID_23854 Human_SNP_ID_656322755 A-to-I Human chr19 - 4110293 4110289 4110293 GTTTTCTTTTTGTTTTTTTGAGAGGCAGTCTCACTCTGTCACTCAGGCTAGAATCTAGTAGTGGC GTTTTCTTTTTGTTTTTTTGAGAGGCAGTCTC____TGTCACTCAGGCTAGAATCTAGTAGTGGC AGAGT A MAP2K2 Ensembl:ENSG00000126934 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1216040329 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_92829,RMVar_hsa_circ_344908,RMVar_hsa_circ_34095,RMVar_hsa_circ_44816,RMVar_hsa_circ_191496 23855 RMVar_ID_23855 Human_SNP_ID_656348308 A-to-I Human chr19 + 4194336 4194335 4194336 CACCGTGCCCAGCTAATTTTTGTATTGTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGG CACCGTGCCCAGCTAATTTTTGTATTGTTAGT_GAGACGGGGTTTCACCATGTTGGCCAGGCTGG TA T ANKRD24 Ensembl:ENSG00000089847 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1324545581 Functional Loss DEL dbSNP153 33..33 33 - - - 23856 RMVar_ID_23856 Human_SNP_ID_656360348 A-to-I Human chr19 + 4229991 4229991 4229991 TCGCCCAGGCTGGAGTACAGTGGCACCATCTCAGCTCACTGAAACCTCCATCTCCTGGGTTCAAG TCGCCCAGGCTGGAGTACAGTGGCACCATCTCTGCTCACTGAAACCTCCATCTCCTGGGTTCAAG A T EBI3 Ensembl:ENSG00000105246 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1454815120 Functional Loss SNV dbSNP153 33..33 33 - - - 23857 RMVar_ID_23857 Human_SNP_ID_656360467 A-to-I Human chr19 + 4230451 4230451 4230451 AAAATTAGCTAGATGTGGTGGCACGTGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGTGGGAGG AAAATTAGCTAGATGTGGTGGCACGTGCCTGTTGTCCCAGCTACTTGGGAGGCTGAGGTGGGAGG A T EBI3 Ensembl:ENSG00000105246 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs900785084 Functional Loss SNV dbSNP153 33..33 33 - - - 23858 RMVar_ID_23858 Human_SNP_ID_656362083 A-to-I Human chr19 + 4235050 4235049 4235051 CACACCCGTTTTTGTTGTTATTGTTTTGAGACAGAGTCTCGCTCTGTCGCCCAGGCAGTGACACA CACACCCGTTTTTGTTGTTATTGTTTTGAGAC__AGTCTCGCTCTGTCGCCCAGGCAGTGACACA CAG C EBI3 Ensembl:ENSG00000105246 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1323233829 Functional Loss DEL dbSNP153 33..34 33 - - - 23859 RMVar_ID_23859 Human_SNP_ID_656362084 A-to-I Human chr19 + 4235050 4235050 4235050 CACACCCGTTTTTGTTGTTATTGTTTTGAGACAGAGTCTCGCTCTGTCGCCCAGGCAGTGACACA CACACCCGTTTTTGTTGTTATTGTTTTGAGACGGAGTCTCGCTCTGTCGCCCAGGCAGTGACACA A G EBI3 Ensembl:ENSG00000105246 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1406194085 Functional Loss SNV dbSNP153 33..33 33 - - - 23860 RMVar_ID_23860 Human_SNP_ID_656362850 A-to-I Human chr19 + 4237775 4237775 4237775 TCCCGACGCCGAGGCGGGCAGATCACGAGGTCAGGAGTTCGAGACCAGCCTGACCAACATGGTGA TCCCGACGCCGAGGCGGGCAGATCACGAGGTCGGGAGTTCGAGACCAGCCTGACCAACATGGTGA A G RF00017-1784 RNACentral:URS0000904F64 SRP RNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs959414102 Functional Loss SNV dbSNP153 33..33 33 - - - 23861 RMVar_ID_23861 Human_SNP_ID_656362923 A-to-I Human chr19 + 4238052 4238052 4238052 GACTCCAGCTGGGTATGGTGGCTCACGCCTGTAATCTCAGCACTTTGGGAGGCCAAGGCAGGTGG GACTCCAGCTGGGTATGGTGGCTCACGCCTGTTATCTCAGCACTTTGGGAGGCCAAGGCAGGTGG A T RF00017-1784 RNACentral:URS0000904F64 SRP RNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs185538359 Functional Loss SNV dbSNP153 33..33 33 - - - 23862 RMVar_ID_23862 Human_SNP_ID_656363246 A-to-I Human chr19 + 4239326 4239326 4239326 GGCCAAGAGCTCCAGACCAACCTGGGCAACATAGTGAGACCCCCATCTCTAAAAAAATAAAATAG GGCCAAGAGCTCCAGACCAACCTGGGCAACATGGTGAGACCCCCATCTCTAAAAAAATAAAATAG A G RF00017-1784 RNACentral:URS0000904F64 SRP RNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1375401643 Functional Loss SNV dbSNP153 33..33 33 - - - 23863 RMVar_ID_23863 Human_SNP_ID_656363302 A-to-I Human chr19 + 4239554 4239554 4239554 CCAGCTACTCGGGAGGCTGAGGCAGAAGAATCACTTGAACCCGGGAGGCGGAGGTTGCAGTGAGC CCAGCTACTCGGGAGGCTGAGGCAGAAGAATCGCTTGAACCCGGGAGGCGGAGGTTGCAGTGAGC A G RF00017-1784 RNACentral:URS0000904F64 SRP RNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1348004374 Functional Loss SNV dbSNP153 33..33 33 - - - 23864 RMVar_ID_23864 Human_SNP_ID_656363488 A-to-I Human chr19 + 4240185 4240185 4240185 TAAAAATTAGCTGGGCTTGGTGGCTCACAGCTATAGTTCCAGCTACTTGGGAGGCCAAAGTGGCA TAAAAATTAGCTGGGCTTGGTGGCTCACAGCTTTAGTTCCAGCTACTTGGGAGGCCAAAGTGGCA A T RF00017-1784 RNACentral:URS0000904F64 SRP RNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1158907811 Functional Loss SNV dbSNP153 33..33 33 - - - 23865 RMVar_ID_23865 Human_SNP_ID_656363734 A-to-I Human chr19 + 4240957 4240957 4240957 GTGAGACCCCGTCTCAAAAAAAAAAGATTAATAGGGATGGGGTCTCACCATGTTCCTCAGACTAG GTGAGACCCCGTCTCAAAAAAAAAAGATTAATTGGGATGGGGTCTCACCATGTTCCTCAGACTAG A T RF00017-1784 RNACentral:URS0000904F64 SRP RNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1405677921 Functional Loss SNV dbSNP153 33..33 33 - - - 23866 RMVar_ID_23866 Human_SNP_ID_656364069 A-to-I Human chr19 + 4242469 4242468 4242470 TTAAACCTTCCATTTTTTTTTTTTCCCGAGACAGAGTCTCTCTCTGTCACCCAGGCTGGGGGGCA TTAAACCTTCCATTTTTTTTTTTTCCCGAGAC__AGTCTCTCTCTGTCACCCAGGCTGGGGGGCA CAG C RF00017-1784 RNACentral:URS0000904F64 SRP RNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1273819507 Functional Loss DEL dbSNP153 33..34 33 - - - 23867 RMVar_ID_23867 Human_SNP_ID_656364441 A-to-I Human chr19 + 4243841 4243841 4243841 AGCTGGGTGTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGTGGATCACC AGCTGGGTGTGGTGGCTCACACCTGTAATCCCGGCACTTTGGGAGGCTGAGGTGGGTGGATCACC A G RF00017-1784 RNACentral:URS0000904F64 SRP RNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs978252349 Functional Loss SNV dbSNP153 33..33 33 - - - 23868 RMVar_ID_23868 Human_SNP_ID_656364474 A-to-I Human chr19 + 4244007 4244007 4244007 AATCCCAGCTACTTGGGAGGCTGAGGTAGGAGAATAGCTTGAACCTGGGAGACGGAGGTTGCGGT AATCCCAGCTACTTGGGAGGCTGAGGTAGGAGGATAGCTTGAACCTGGGAGACGGAGGTTGCGGT A G RF00017-1784 RNACentral:URS0000904F64 SRP RNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs780743040 Functional Loss SNV dbSNP153 33..33 33 - - - 23869 RMVar_ID_23869 Human_SNP_ID_656364570 A-to-I Human chr19 + 4244294 4244293 4244294 GGCACGATCTTGGCACGATCTTGGCTCACTGCAACCTCCACCTGCCAGGTTCAAGCGATTCTCCT GGCACGATCTTGGCACGATCTTGGCTCACTGC_ACCTCCACCTGCCAGGTTCAAGCGATTCTCCT CA C RF00017-1784 RNACentral:URS0000904F64 SRP RNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs747742293 Functional Loss DEL dbSNP153 33..33 33 - - - 23870 RMVar_ID_23870 Human_SNP_ID_656364783 A-to-I Human chr19 + 4245110 4245110 4245110 CCTGCCTCAGCCTCCCAAGCAGCTGGGATTACAGGCATGCACCACCATGCCCGGCTAATTTTGTA CCTGCCTCAGCCTCCCAAGCAGCTGGGATTACGGGCATGCACCACCATGCCCGGCTAATTTTGTA A G RF00017-1784 RNACentral:URS0000904F64 SRP RNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs983944406 Functional Loss SNV dbSNP153 33..33 33 - - - 23871 RMVar_ID_23871 Human_SNP_ID_656364792 A-to-I Human chr19 + 4245134 4245134 4245134 GGGATTACAGGCATGCACCACCATGCCCGGCTAATTTTGTATTTTTAGTAGAGACAAGATTTCTT GGGATTACAGGCATGCACCACCATGCCCGGCTGATTTTGTATTTTTAGTAGAGACAAGATTTCTT A G RF00017-1784 RNACentral:URS0000904F64 SRP RNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1397663789 Functional Loss SNV dbSNP153 33..33 33 - - - 23872 RMVar_ID_23872 Human_SNP_ID_656364886 A-to-I Human chr19 + 4245400 4245396 4245400 TCTCTTTTTTTTTTTTTTTGAGATGGAGTCTCACTCTGTCGCCCAGGCCACAGGGCAGCGGCACA TCTCTTTTTTTTTTTTTTTGAGATGGAGT____CTCTGTCGCCCAGGCCACAGGGCAGCGGCACA TCTCA T RF00017-1784 RNACentral:URS0000904F64 SRP RNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs539715020 Functional Loss DEL dbSNP153 30..33 33 - - - 23873 RMVar_ID_23873 Human_SNP_ID_656370798 A-to-I Human chr19 + 4264447 4264447 4264447 CTCCCACCTCAGTCTCCTGAGCAGCTGGGACCACAGGCACGCACCACCACGCCTGGCTAATTTTT CTCCCACCTCAGTCTCCTGAGCAGCTGGGACCGCAGGCACGCACCACCACGCCTGGCTAATTTTT A G YJU2 Ensembl:ENSG00000105248 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs916503445 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 23874 RMVar_ID_23874 Human_SNP_ID_656370903 A-to-I Human chr19 + 4264748 4264748 4264748 ACCTCAGGTGATTCACCTGACTCGGCCGCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGTGC ACCTCAGGTGATTCACCTGACTCGGCCGCCCATAGTGCTGGGATTACAGGCGTGAGCCACTGTGC A T YJU2 Ensembl:ENSG00000105248 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs188943099 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 23875 RMVar_ID_23875 Human_SNP_ID_656371029 A-to-I Human chr19 + 4265265 4265265 4265265 TGCGTTTTCTTGGTTTATTTTATTTTTATTTTAGAGATGAGGTCTTGCTCTGTCACCCAGGCTGG TGCGTTTTCTTGGTTTATTTTATTTTTATTTTGGAGATGAGGTCTTGCTCTGTCACCCAGGCTGG A G YJU2 Ensembl:ENSG00000105248 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs904949674 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6766773 RMVar_hsa_circ_112665,RMVar_hsa_circ_114032,RMVar_hsa_circ_191509,RMVar_hsa_circ_76601,RMVar_hsa_circ_191510,RMVar_hsa_circ_191511 23876 RMVar_ID_23876 Human_SNP_ID_656371334 A-to-I Human chr19 + 4266404 4266404 4266404 TGAATCACACTGTGGCTTCTCATCACGCCTTTACCCATGCCATTCCCCTTACCTGGGATGCCCCC TGAATCACACTGTGGCTTCTCATCACGCCTTTGCCCATGCCATTCCCCTTACCTGGGATGCCCCC A G YJU2 Ensembl:ENSG00000105248 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1312898643 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 23877 RMVar_ID_23877 Human_SNP_ID_656371455 A-to-I Human chr19 + 4266834 4266834 4266834 GAGATCCCGTCTCTACAAAAATTAAAAATGTTAGCCTGCCATGGTGGCGTGCACCTGCAGGAGGC GAGATCCCGTCTCTACAAAAATTAAAAATGTTTGCCTGCCATGGTGGCGTGCACCTGCAGGAGGC A T YJU2 Ensembl:ENSG00000105248 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs548333756 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 23878 RMVar_ID_23878 Human_SNP_ID_656372869 A-to-I Human chr19 + 4271277 4271277 4271277 TTTTTTTTTTTTTTGAGACAGCATCTCACTCTATCACCCCCGCTGGAGTGCAGTGGCAGGATCTC TTTTTTTTTTTTTTGAGACAGCATCTCACTCTTTCACCCCCGCTGGAGTGCAGTGGCAGGATCTC A T RF00017-1784 RNACentral:URS0000904F64 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs757602594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13463495 23879 RMVar_ID_23879 Human_SNP_ID_656399919 A-to-I Human chr19 + 4354679 4354679 4354679 CCTGAACTCAGGAGTTCGAGACAAGCCTGGGTAACACTGAAACCCTGTCTCTACTAAATATACAA CCTGAACTCAGGAGTTCGAGACAAGCCTGGGTGACACTGAAACCCTGTCTCTACTAAATATACAA A G MPND Ensembl:ENSG00000008382 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1186158066 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27165,RMVar_hsa_circ_338556,RMVar_hsa_circ_191521 23880 RMVar_ID_23880 Human_SNP_ID_656400456 A-to-I Human chr19 + 4356104 4356104 4356104 TCAAACTCCTGACCTCGTGATCCACCCGCGTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG TCAAACTCCTGACCTCGTGATCCACCCGCGTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG A G MPND Ensembl:ENSG00000008382 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1453648124 Functional Loss SNV dbSNP153 33..33 33 - - - 23881 RMVar_ID_23881 Human_SNP_ID_656407854 A-to-I Human chr19 - 4377301 4377301 4377301 CCTCCTCCCTGCTGGCAGCCAGGCAGGGATTTAGGCGGTTTCTGTTTGGCCTCCAGTGCTTGCCT CCTCCTCCCTGCTGGCAGCCAGGCAGGGATTTGGGCGGTTTCTGTTTGGCCTCCAGTGCTTGCCT T C SH3GL1 Ensembl:ENSG00000141985 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs939391362 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92594,RMVar_hsa_circ_191524 23882 RMVar_ID_23882 Human_SNP_ID_656407892 A-to-I Human chr19 - 4377417 4377417 4377417 GAGCCTGGTGTCCCTGTGTAAGTGTGCCAGATAGGCAGAGGAGACAGGTGAAGGCACATTCCTCA GAGCCTGGTGTCCCTGTGTAAGTGTGCCAGATGGGCAGAGGAGACAGGTGAAGGCACATTCCTCA T C SH3GL1 Ensembl:ENSG00000141985 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs369229518 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92594,RMVar_hsa_circ_191524 23883 RMVar_ID_23883 Human_SNP_ID_656410923 A-to-I Human chr19 - 4386997 4386997 4386997 GGGAGGCAGAGCTTGCAGTGAGCCAAGATTGCACCACTGCACTCCAGCCTGGGCGACAGAGCAAG GGGAGGCAGAGCTTGCAGTGAGCCAAGATTGCGCCACTGCACTCCAGCCTGGGCGACAGAGCAAG T C SH3GL1 Ensembl:ENSG00000141985 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs183662732 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92594,RMVar_hsa_circ_191524 23884 RMVar_ID_23884 Human_SNP_ID_656415946 A-to-I Human chr19 + 4403994 4403994 4403994 GGCCTGCACCACCATGCCTGGCTAATTTTTGTATTTTTTAGTAGAGACGGGGTTTCACCATGTTG GGCCTGCACCACCATGCCTGGCTAATTTTTGTGTTTTTTAGTAGAGACGGGGTTTCACCATGTTG A G CHAF1A Ensembl:ENSG00000167670 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs898428926 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117327,RMVar_hsa_circ_191530 23885 RMVar_ID_23885 Human_SNP_ID_656416317 A-to-I Human chr19 + 4405487 4405487 4405487 AAAATTAGCCGAGAGTGGTGGCATGCGCCTGTAGTCCCAGCTACTTGAGAGAGTGAGGCAGGAGA AAAATTAGCCGAGAGTGGTGGCATGCGCCTGTGGTCCCAGCTACTTGAGAGAGTGAGGCAGGAGA A G CHAF1A Ensembl:ENSG00000167670 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs142182268 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117327,RMVar_hsa_circ_191530 23886 RMVar_ID_23886 Human_SNP_ID_656417032 A-to-I Human chr19 + 4408059 4408057 4408059 TTGAGACGAGGTCCCTTTTGCCCAGGCTGCAGAGTAGTTGCACCACCACAGCTCACTGCAGCCTC TTGAGACGAGGTCCCTTTTGCCCAGGCTGCGGGGTAGTTGCACCACCACAGCTCACTGCAGCCTC AGA GGG CHAF1A Ensembl:ENSG00000167670 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs386806123 Functional Loss MNV dbSNP153 31..33 33 - - - 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 23887 RMVar_ID_23887 Human_SNP_ID_656417036 A-to-I Human chr19 + 4408059 4408059 4408059 TTGAGACGAGGTCCCTTTTGCCCAGGCTGCAGAGTAGTTGCACCACCACAGCTCACTGCAGCCTC TTGAGACGAGGTCCCTTTTGCCCAGGCTGCAGGGTAGTTGCACCACCACAGCTCACTGCAGCCTC A G CHAF1A Ensembl:ENSG00000167670 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs424682 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2289,GWAS_ID_2290,GWAS_ID_2291,GWAS_ID_2292,GWAS_ID_2293,GWAS_ID_2294,GWAS_ID_2295,GWAS_ID_2296 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 23888 RMVar_ID_23888 Human_SNP_ID_656417037 A-to-I Human chr19 + 4408059 4408059 4408059 TTGAGACGAGGTCCCTTTTGCCCAGGCTGCAGAGTAGTTGCACCACCACAGCTCACTGCAGCCTC TTGAGACGAGGTCCCTTTTGCCCAGGCTGCAGTGTAGTTGCACCACCACAGCTCACTGCAGCCTC A T CHAF1A Ensembl:ENSG00000167670 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs424682 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2289,GWAS_ID_2290,GWAS_ID_2291,GWAS_ID_2292,GWAS_ID_2293,GWAS_ID_2294,GWAS_ID_2295,GWAS_ID_2296 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 23889 RMVar_ID_23889 Human_SNP_ID_656417149 A-to-I Human chr19 + 4408399 4408399 4408399 TACTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGGTCTCGATCTCCTGACCTTGTGA TACTTTTAGTAGAGACGGGGTTTCACCGTGTTTGCCAGGATGGTCTCGATCTCCTGACCTTGTGA A T CHAF1A Ensembl:ENSG00000167670 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1056351423 Functional Loss SNV dbSNP153 33..33 33 - - - 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 23890 RMVar_ID_23890 Human_SNP_ID_656417281 A-to-I Human chr19 + 4408672 4408672 4408672 AATTTTTGTAGTTTTAGAAAAGACGGGGTTTCACCATTTTGGTCTGGCTGGTCTCAAACTCCTGA AATTTTTGTAGTTTTAGAAAAGACGGGGTTTCGCCATTTTGGTCTGGCTGGTCTCAAACTCCTGA A G CHAF1A Ensembl:ENSG00000167670 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs567327978 Functional Loss SNV dbSNP153 33..33 33 - - - 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 23891 RMVar_ID_23891 Human_SNP_ID_656417299 A-to-I Human chr19 + 4408735 4408735 4408735 GACCTTGTGATCTGCTTGCCTCGGCCTCCCCAAAGTGCTGGGATTACAGGCATGAGCCACCACAC GACCTTGTGATCTGCTTGCCTCGGCCTCCCCAGAGTGCTGGGATTACAGGCATGAGCCACCACAC A G CHAF1A Ensembl:ENSG00000167670 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1429861376 Functional Loss SNV dbSNP153 33..33 33 - - - 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 23892 RMVar_ID_23892 Human_SNP_ID_656417300 A-to-I Human chr19 + 4408735 4408735 4408735 GACCTTGTGATCTGCTTGCCTCGGCCTCCCCAAAGTGCTGGGATTACAGGCATGAGCCACCACAC GACCTTGTGATCTGCTTGCCTCGGCCTCCCCATAGTGCTGGGATTACAGGCATGAGCCACCACAC A T CHAF1A Ensembl:ENSG00000167670 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1429861376 Functional Loss SNV dbSNP153 33..33 33 - - - 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 23893 RMVar_ID_23893 Human_SNP_ID_656417305 A-to-I Human chr19 + 4408754 4408754 4408754 CTCGGCCTCCCCAAAGTGCTGGGATTACAGGCATGAGCCACCACACCCGGCCCAGATAGTCCCTT CTCGGCCTCCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCACACCCGGCCCAGATAGTCCCTT A G CHAF1A Ensembl:ENSG00000167670 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs243347 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2297,GWAS_ID_2298,GWAS_ID_2299,GWAS_ID_2300,GWAS_ID_2301,GWAS_ID_2302,GWAS_ID_2303,GWAS_ID_2304 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 23894 RMVar_ID_23894 Human_SNP_ID_656417306 A-to-I Human chr19 + 4408754 4408754 4408754 CTCGGCCTCCCCAAAGTGCTGGGATTACAGGCATGAGCCACCACACCCGGCCCAGATAGTCCCTT CTCGGCCTCCCCAAAGTGCTGGGATTACAGGCTTGAGCCACCACACCCGGCCCAGATAGTCCCTT A T CHAF1A Ensembl:ENSG00000167670 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs243347 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2297,GWAS_ID_2298,GWAS_ID_2299,GWAS_ID_2300,GWAS_ID_2301,GWAS_ID_2302,GWAS_ID_2303,GWAS_ID_2304 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 23895 RMVar_ID_23895 Human_SNP_ID_656417947 A-to-I Human chr19 + 4410530 4410530 4410530 AGCATCCCTGATAGCTGGGATTACAGGTGCGCACCACCACACTTGGCTAATTTTTATATTTTTAG AGCATCCCTGATAGCTGGGATTACAGGTGCGCTCCACCACACTTGGCTAATTTTTATATTTTTAG A T CHAF1A Ensembl:ENSG00000167670 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1477872378 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51508,RMVar_hsa_circ_80859,RMVar_hsa_circ_124674,RMVar_hsa_circ_291666,RMVar_hsa_circ_89465,RMVar_hsa_circ_123090,RMVar_hsa_circ_191532,RMVar_hsa_circ_191533,RMVar_hsa_circ_191534,RMVar_hsa_circ_191537 23896 RMVar_ID_23896 Human_SNP_ID_656417998 A-to-I Human chr19 + 4410712 4410712 4410712 CCTGCAAAAAAATTTTTAAAAGTTATCCAGGCATGGTGGCACATGCCTGTAGTCCCAGCCACCTG CCTGCAAAAAAATTTTTAAAAGTTATCCAGGCGTGGTGGCACATGCCTGTAGTCCCAGCCACCTG A G CHAF1A Ensembl:ENSG00000167670 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs953558400 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51508,RMVar_hsa_circ_80859,RMVar_hsa_circ_124674,RMVar_hsa_circ_291666,RMVar_hsa_circ_89465,RMVar_hsa_circ_123090,RMVar_hsa_circ_191532,RMVar_hsa_circ_191533,RMVar_hsa_circ_191534,RMVar_hsa_circ_191537 23897 RMVar_ID_23897 Human_SNP_ID_656418324 A-to-I Human chr19 + 4411765 4411765 4411765 CACCTTCTAGGTTCAAGCGATTTTCCTGCGTCAGCCTCTTGAGTAGCTGGGATTACAGGTGCCCA CACCTTCTAGGTTCAAGCGATTTTCCTGCGTCGGCCTCTTGAGTAGCTGGGATTACAGGTGCCCA A G CHAF1A Ensembl:ENSG00000167670 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs936432275 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51508,RMVar_hsa_circ_80859,RMVar_hsa_circ_124674,RMVar_hsa_circ_291666,RMVar_hsa_circ_89465,RMVar_hsa_circ_123090,RMVar_hsa_circ_191532,RMVar_hsa_circ_191533,RMVar_hsa_circ_191534,RMVar_hsa_circ_191537 23898 RMVar_ID_23898 Human_SNP_ID_656420273 A-to-I Human chr19 + 4418962 4418962 4418962 TCGGCTCACTGCAACCTCTGCCTCCCGGGTTCAAGCGGTTCTTCTGCCTCAGCCTCCCGAGTAGC TCGGCTCACTGCAACCTCTGCCTCCCGGGTTCGAGCGGTTCTTCTGCCTCAGCCTCCCGAGTAGC A G CHAF1A Ensembl:ENSG00000167670 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1056044373 Functional Loss SNV dbSNP153 33..33 33 - - - 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 23899 RMVar_ID_23899 Human_SNP_ID_656420800 A-to-I Human chr19 + 4420686 4420686 4420686 AAACAAGGCTGGGCGTAGTGGCTCGCCCCCATAATCCCACACTTTGGGAGGCCAAAGTGGGAGGA AAACAAGGCTGGGCGTAGTGGCTCGCCCCCATCATCCCACACTTTGGGAGGCCAAAGTGGGAGGA A C CHAF1A Ensembl:ENSG00000167670 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1413200839 Functional Loss SNV dbSNP153 33..33 33 - - - 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 23900 RMVar_ID_23900 Human_SNP_ID_656420819 A-to-I Human chr19 + 4420768 4420768 4420768 TTTGAGACAAGCCTGGGCAACGTAGTGTCTCTACTAAAAAGAAAAAGAATTCCTGGGCTGGTTGC TTTGAGACAAGCCTGGGCAACGTAGTGTCTCTGCTAAAAAGAAAAAGAATTCCTGGGCTGGTTGC A G CHAF1A Ensembl:ENSG00000167670 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs534279369 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13467985 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 23901 RMVar_ID_23901 Human_SNP_ID_656420848 A-to-I Human chr19 + 4420870 4420870 4420870 TGAGGTGGACAGATTGCTTGAGCGCAGGAGTTAAAGATCAGTCTGGGCAACATAGTGAGACTCCA TGAGGTGGACAGATTGCTTGAGCGCAGGAGTTCAAGATCAGTCTGGGCAACATAGTGAGACTCCA A C CHAF1A Ensembl:ENSG00000167670 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1568434770 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13467991,Human_RBP_ID_25421455 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 23902 RMVar_ID_23902 Human_SNP_ID_656420872 A-to-I Human chr19 + 4420953 4420953 4420953 AGGTGTGGTGACAGGTGCCTGTGGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGGACTGATTTGA AGGTGTGGTGACAGGTGCCTGTGGTCCCAGCTGCTCGGGAGGCTGAGGCAGGAGGACTGATTTGA A G CHAF1A Ensembl:ENSG00000167670 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1456907037 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13467993 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 23903 RMVar_ID_23903 Human_SNP_ID_656421011 A-to-I Human chr19 + 4421519 4421519 4421519 ACTTCTGTGGCTGGGTGCTGGGGCTCATGCCTATAATTCCAACACTTTGGGAGGCTAAGGCAGAA ACTTCTGTGGCTGGGTGCTGGGGCTCATGCCTGTAATTCCAACACTTTGGGAGGCTAAGGCAGAA A G CHAF1A Ensembl:ENSG00000167670 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs371922584 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13468020,Human_RBP_ID_17567877 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 23904 RMVar_ID_23904 Human_SNP_ID_656424864 A-to-I Human chr19 + 4434271 4434271 4434271 AGGAGGCTAAGGCGGGAGGATTACTGGAGCCTAGGAGATTGAGGCTGCAGTGAGCTATGATCATG AGGAGGCTAAGGCGGGAGGATTACTGGAGCCTCGGAGATTGAGGCTGCAGTGAGCTATGATCATG A C CHAF1A Ensembl:ENSG00000167670 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1482091052 Functional Loss SNV dbSNP153 33..33 33 - - - 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 23905 RMVar_ID_23905 Human_SNP_ID_656425350 A-to-I Human chr19 + 4435883 4435880 4435883 GTCGTTGGCTGGGCACAGTGGCTCACGCCTATAATCCCATCACTTTGGGAGGCCAAGGCGGGCAG GTCGTTGGCTGGGCACAGTGGCTCACGCCT___ATCCCATCACTTTGGGAGGCCAAGGCGGGCAG TATA T CHAF1A Ensembl:ENSG00000167670 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1398481151 Functional Loss DEL dbSNP153 31..33 33 - - - 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 23906 RMVar_ID_23906 Human_SNP_ID_656426121 A-to-I Human chr19 + 4438433 4438433 4438433 TTGCCCAGGCTGGTCTTTGAACTTGTGGGCTCAAGCAATCCACCTGCCTCGGCCTCCCAAAGTAC TTGCCCAGGCTGGTCTTTGAACTTGTGGGCTCGAGCAATCCACCTGCCTCGGCCTCCCAAAGTAC A G CHAF1A Ensembl:ENSG00000167670 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs752384568 Functional Loss SNV dbSNP153 33..33 33 - - - 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 23907 RMVar_ID_23907 Human_SNP_ID_656426644 A-to-I Human chr19 + 4440366 4440366 4440366 CGGTGGCTCACACCTTGTCATCCCAGCACTTTAGGAGGCCGAGGTGGAAGGATGGCTTGAGCCCA CGGTGGCTCACACCTTGTCATCCCAGCACTTTGGGAGGCCGAGGTGGAAGGATGGCTTGAGCCCA A G CHAF1A Ensembl:ENSG00000167670 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1468377834 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1294792 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 23908 RMVar_ID_23908 Human_SNP_ID_656426668 A-to-I Human chr19 + 4440462 4440462 4440462 CCCCCTTGTCTCTACTTAAAAAAAAAAAAATTAGCTGGGCGTGATGGCGGGTGCCTGTAGTCCCA CCCCCTTGTCTCTACTTAAAAAAAAAAAAATTGGCTGGGCGTGATGGCGGGTGCCTGTAGTCCCA A G CHAF1A Ensembl:ENSG00000167670 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs912998344 Functional Loss SNV dbSNP153 33..33 33 - - - 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 23909 RMVar_ID_23909 Human_SNP_ID_656428382 A-to-I Human chr19 - 4445404 4445404 4445404 CCGCCACCCCAGGGCCTCCAAGCCACCTCTGGAAATACTTGGCTCTGCCCCATGGGCACGGGAGG CCGCCACCCCAGGGCCTCCAAGCCACCTCTGGGAATACTTGGCTCTGCCCCATGGGCACGGGAGG T C UBXN6 Ensembl:ENSG00000167671 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs993825220 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17656610,Human_RBP_ID_17926703,Human_RBP_ID_27468864 RMVar_hsa_circ_105129,RMVar_hsa_circ_114592,RMVar_hsa_circ_124179,RMVar_hsa_circ_109032,RMVar_hsa_circ_191547,RMVar_hsa_circ_80900,RMVar_hsa_circ_91957,RMVar_hsa_circ_191549,RMVar_hsa_circ_191551,RMVar_hsa_circ_75955,RMVar_hsa_circ_191550,RMVar_hsa_circ_191548,RMVar_hsa_circ_191545,RMVar_hsa_circ_191546 23910 RMVar_ID_23910 Human_SNP_ID_656430743 A-to-I Human chr19 - 4451325 4451325 4451325 GGCTGGGCGCGGTGGCTCTTGCCTGTAATTCCAGTGCTTTGGGAGGCTGAGGCAGGTGGATCACC GGCTGGGCGCGGTGGCTCTTGCCTGTAATTCCTGTGCTTTGGGAGGCTGAGGCAGGTGGATCACC T A UBXN6 Ensembl:ENSG00000167671 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1433360160 Functional Loss SNV dbSNP153 33..33 33 - - - 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_23167 23911 RMVar_ID_23911 Human_SNP_ID_656430745 A-to-I Human chr19 - 4451330 4451330 4451330 TAAGTGGCTGGGCGCGGTGGCTCTTGCCTGTAATTCCAGTGCTTTGGGAGGCTGAGGCAGGTGGA TAAGTGGCTGGGCGCGGTGGCTCTTGCCTGTACTTCCAGTGCTTTGGGAGGCTGAGGCAGGTGGA T G UBXN6 Ensembl:ENSG00000167671 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1433750713 Functional Loss SNV dbSNP153 33..33 33 - - - 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_23167 23912 RMVar_ID_23912 Human_SNP_ID_656430746 A-to-I Human chr19 - 4451331 4451331 4451331 GTAAGTGGCTGGGCGCGGTGGCTCTTGCCTGTAATTCCAGTGCTTTGGGAGGCTGAGGCAGGTGG GTAAGTGGCTGGGCGCGGTGGCTCTTGCCTGTTATTCCAGTGCTTTGGGAGGCTGAGGCAGGTGG T A UBXN6 Ensembl:ENSG00000167671 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs914198107 Functional Loss SNV dbSNP153 33..33 33 - - - 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_23167 23913 RMVar_ID_23913 Human_SNP_ID_656440485 A-to-I Human chr19 + 4479116 4479116 4479116 TGGGAGGCCAAGGGGGCAGATCACTTCAGGTCAGGAGTTCCAGACCAGCCTGTTCAACATGGCGA TGGGAGGCCAAGGGGGCAGATCACTTCAGGTCGGGAGTTCCAGACCAGCCTGTTCAACATGGCGA A G HDGFL2 Ensembl:ENSG00000167674 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1205211133 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19635,RMVar_hsa_circ_334157 23914 RMVar_ID_23914 Human_SNP_ID_656496961 A-to-I Human chr19 + 4653291 4653291 4653291 GTGCCACTGCACTCCAGCCTGGGTGACAGAGCAAGACTCTGTCTCAAAAAAAGAAGCGGGGGAGT GTGCCACTGCACTCCAGCCTGGGTGACAGAGCGAGACTCTGTCTCAAAAAAAGAAGCGGGGGAGT A G TNFAIP8L1 Ensembl:ENSG00000185361 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs754131158 Functional Loss SNV dbSNP153 33..33 33 - - - 23915 RMVar_ID_23915 Human_SNP_ID_656496993 A-to-I Human chr19 + 4653414 4653414 4653414 GAGGCAGGAAGATTGCTTGAACTCAGAAGTTCAAGACCAGTCTGGGCAACATGGTGAGACCCTCG GAGGCAGGAAGATTGCTTGAACTCAGAAGTTCGAGACCAGTCTGGGCAACATGGTGAGACCCTCG A G TNFAIP8L1 Ensembl:ENSG00000185361 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,29129909,31158229,31158229,31158229,32596459,32596459 RNA-Seq:(High) rs1466858607 Functional Loss SNV dbSNP153 33..33 33 - - - 23916 RMVar_ID_23916 Human_SNP_ID_656497285 A-to-I Human chr19 + 4654367 4654366 4654368 GTGCACATTTTATTTATTTATTGTTTTGAGACAAAGTCTCGCTGTGTCACCCAGGCTGGAGTGCA GTGCACATTTTATTTATTTATTGTTTTGAGAC__AGTCTCGCTGTGTCACCCAGGCTGGAGTGCA CAA C TNFAIP8L1 Ensembl:ENSG00000185361 Protein coding 3'UTR GSE47997;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs1368106817 Functional Loss DEL dbSNP153 33..34 33 - - - 23917 RMVar_ID_23917 Human_SNP_ID_656497285 A-to-I Human chr19 + 4654368 4654366 4654368 TGCACATTTTATTTATTTATTGTTTTGAGACAAAGTCTCGCTGTGTCACCCAGGCTGGAGTGCAG TGCACATTTTATTTATTTATTGTTTTGAGAC__AGTCTCGCTGTGTCACCCAGGCTGGAGTGCAG CAA C TNFAIP8L1 Ensembl:ENSG00000185361 Protein coding 3'UTR GSE47997;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1368106817 Functional Loss DEL dbSNP153 32..33 33 - - - 23918 RMVar_ID_23918 Human_SNP_ID_656497313 A-to-I Human chr19 + 4654461 4654461 4654461 TTCCTTCCAGGCTCAAGTGATCCTCCCACCTCAGCCCCGGGTAGCTGGGACTACAGGTGTGCACG TTCCTTCCAGGCTCAAGTGATCCTCCCACCTCCGCCCCGGGTAGCTGGGACTACAGGTGTGCACG A C TNFAIP8L1 Ensembl:ENSG00000185361 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1051850910 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26471826 Human_miRNA_ID_582920 23919 RMVar_ID_23919 Human_SNP_ID_656497335 A-to-I Human chr19 + 4654531 4654528 4654531 ACCCGGCTAATCTTTGTATTTTTTGTAGACAGAAGGTCTCACCATGTTGCCCAGGATGGTCTCGA ACCCGGCTAATCTTTGTATTTTTTGTAGAC___AGGTCTCACCATGTTGCCCAGGATGGTCTCGA CAGA C TNFAIP8L1 Ensembl:ENSG00000185361 Protein coding 3'UTR GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs1458674582 Functional Loss DEL dbSNP153 31..33 33 - - - 23920 RMVar_ID_23920 Human_SNP_ID_656497966 A-to-I Human chr19 - 4656791 4656790 4656792 CACCAGGAGTTCAAGACCAGCTTAGGCAACATAGCAAGACCCCCATCTCTACCAAAAAATAAATA CACCAGGAGTTCAAGACCAGCTTAGGCAACA__GCAAGACCCCCATCTCTACCAAAAAATAAATA CTA C MYDGF Ensembl:ENSG00000074842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1394512481 Functional Loss DEL dbSNP153 32..33 33 - - - 23921 RMVar_ID_23921 Human_SNP_ID_656501145 A-to-I Human chr19 - 4666821 4666821 4666821 CCTCAAATGATCAGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGGTGC CCTCAAATGATCAGCCTGCCTCGGCCTCCCAACGTGCTGGGATTACAGGTGTGAGCCACCGGTGC T G MYDGF Ensembl:ENSG00000074842 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1292587595 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125241,RMVar_hsa_circ_191586 23922 RMVar_ID_23922 Human_SNP_ID_656501379 A-to-I Human chr19 - 4667547 4667547 4667547 ATGATTTGGGCCAGGCACAGTGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCCAAGGCTGGC ATGATTTGGGCCAGGCACAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCTGGC T C MYDGF Ensembl:ENSG00000074842 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs767631687 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125241,RMVar_hsa_circ_191586 23923 RMVar_ID_23923 Human_SNP_ID_656510978 A-to-I Human chr19 - 4696971 4696971 4696971 CCTCAGCCTCCTGAGTAGAGGGGACTATAGGTACTCGCCACTATGCCTGGCCAATGTTTTGTATT CCTCAGCCTCCTGAGTAGAGGGGACTATAGGTGCTCGCCACTATGCCTGGCCAATGTTTTGTATT T C DPP9 Ensembl:ENSG00000142002 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs868541440 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13551360 RMVar_hsa_circ_1260,RMVar_hsa_circ_71398,RMVar_hsa_circ_191589,RMVar_hsa_circ_121173,RMVar_hsa_circ_14215,RMVar_hsa_circ_360878,RMVar_hsa_circ_69356,RMVar_hsa_circ_117386,RMVar_hsa_circ_40324,RMVar_hsa_circ_4556,RMVar_hsa_circ_191592,RMVar_hsa_circ_191594,RMVar_hsa_circ_114451,RMVar_hsa_circ_361374,RMVar_hsa_circ_191593 23924 RMVar_ID_23924 Human_SNP_ID_656510979 A-to-I Human chr19 - 4696977 4696977 4696977 CTCCCACCTCAGCCTCCTGAGTAGAGGGGACTATAGGTACTCGCCACTATGCCTGGCCAATGTTT CTCCCACCTCAGCCTCCTGAGTAGAGGGGACTGTAGGTACTCGCCACTATGCCTGGCCAATGTTT T C DPP9 Ensembl:ENSG00000142002 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1352937569 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13551360 RMVar_hsa_circ_1260,RMVar_hsa_circ_71398,RMVar_hsa_circ_191589,RMVar_hsa_circ_121173,RMVar_hsa_circ_14215,RMVar_hsa_circ_360878,RMVar_hsa_circ_69356,RMVar_hsa_circ_117386,RMVar_hsa_circ_40324,RMVar_hsa_circ_4556,RMVar_hsa_circ_191592,RMVar_hsa_circ_191594,RMVar_hsa_circ_114451,RMVar_hsa_circ_361374,RMVar_hsa_circ_191593 23925 RMVar_ID_23925 Human_SNP_ID_656513258 A-to-I Human chr19 - 4704935 4704935 4704935 ATAGTGCAGTGGCGCAATCTCGGCTCACTGCAACCTCTGCCTCCCGGTTCAAGTGATTCTTCTGC ATAGTGCAGTGGCGCAATCTCGGCTCACTGCAGCCTCTGCCTCCCGGTTCAAGTGATTCTTCTGC T C DPP9 Ensembl:ENSG00000142002 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1207639347 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71398,RMVar_hsa_circ_117386,RMVar_hsa_circ_4556,RMVar_hsa_circ_191594,RMVar_hsa_circ_361374,RMVar_hsa_circ_112070,RMVar_hsa_circ_95981,RMVar_hsa_circ_41179,RMVar_hsa_circ_191595,RMVar_hsa_circ_319102,RMVar_hsa_circ_191596,RMVar_hsa_circ_191597 23926 RMVar_ID_23926 Human_SNP_ID_656513267 A-to-I Human chr19 - 4704967 4704967 4704967 TTGAGACAAAGTCTCACTCTGTCACTCAGGCTATAGTGCAGTGGCGCAATCTCGGCTCACTGCAA TTGAGACAAAGTCTCACTCTGTCACTCAGGCTGTAGTGCAGTGGCGCAATCTCGGCTCACTGCAA T C DPP9 Ensembl:ENSG00000142002 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1057439429 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13479397 RMVar_hsa_circ_71398,RMVar_hsa_circ_117386,RMVar_hsa_circ_4556,RMVar_hsa_circ_191594,RMVar_hsa_circ_361374,RMVar_hsa_circ_112070,RMVar_hsa_circ_95981,RMVar_hsa_circ_41179,RMVar_hsa_circ_191595,RMVar_hsa_circ_319102,RMVar_hsa_circ_191596,RMVar_hsa_circ_191597 23927 RMVar_ID_23927 Human_SNP_ID_656513344 A-to-I Human chr19 - 4705316 4705316 4705316 GGTAGGCTGAGATGGGAGGATCTCTTGAACCCAGGAGGGCAAGGCTACAGTGAGCCGTGATCTCA GGTAGGCTGAGATGGGAGGATCTCTTGAACCCGGGAGGGCAAGGCTACAGTGAGCCGTGATCTCA T C DPP9 Ensembl:ENSG00000142002 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1392388217 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71398,RMVar_hsa_circ_117386,RMVar_hsa_circ_4556,RMVar_hsa_circ_191594,RMVar_hsa_circ_361374,RMVar_hsa_circ_112070,RMVar_hsa_circ_95981,RMVar_hsa_circ_41179,RMVar_hsa_circ_191595,RMVar_hsa_circ_319102,RMVar_hsa_circ_191596,RMVar_hsa_circ_191597 23928 RMVar_ID_23928 Human_SNP_ID_656516323 A-to-I Human chr19 - 4716386 4716386 4716386 TGATCCTCCTGCCTTGGCCTCCCGAAGTGCTGAGATTACAGGCATGAGCCACTGTGCCCGGCCAA TGATCCTCCTGCCTTGGCCTCCCGAAGTGCTGGGATTACAGGCATGAGCCACTGTGCCCGGCCAA T C DPP9 Ensembl:ENSG00000142002 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10153468 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117386,RMVar_hsa_circ_191594,RMVar_hsa_circ_361374 23929 RMVar_ID_23929 Human_SNP_ID_656519362 A-to-I Human chr19 + 4725468 4725468 4725468 GCCCGCCTGCAGCCTCCCAAAGTACTGGGATTACAGGCATGAGCCACCGCGCCCGACCCCAACTA GCCCGCCTGCAGCCTCCCAAAGTACTGGGATTGCAGGCATGAGCCACCGCGCCCGACCCCAACTA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167735868 Functional Loss SNV dbSNP153 33..33 33 - - - 23930 RMVar_ID_23930 Human_SNP_ID_656540691 A-to-I Human chr19 + 4795769 4795769 4795769 TCCCCCAGGCTGGAGTGCAATGGCGCGATCTCAGCTCACTGCAACCTCTGCCTCCTGGGTTCAAA TCCCCCAGGCTGGAGTGCAATGGCGCGATCTCTGCTCACTGCAACCTCTGCCTCCTGGGTTCAAA A T FEM1A Ensembl:ENSG00000141965 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs987011753 Functional Loss SNV dbSNP153 33..33 33 - - - 23931 RMVar_ID_23931 Human_SNP_ID_656540719 A-to-I Human chr19 + 4795896 4795895 4795896 TTTTTGTATTTTCTGTAGAGGCAGGTTTTGCCATGTTGGCCAGGCTGGTCTCAAACTCCTGAACT TTTTTGTATTTTCTGTAGAGGCAGGTTTTGCC_TGTTGGCCAGGCTGGTCTCAAACTCCTGAACT CA C FEM1A Ensembl:ENSG00000141965 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1183524531 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_6776666 23932 RMVar_ID_23932 Human_SNP_ID_656540861 A-to-I Human chr19 + 4796365 4796365 4796365 AGGCATACACCACCATGCCTGGCTAATTGTGTATTTTTAGCAGAGACGGGGTTTCACCATATTGG AGGCATACACCACCATGCCTGGCTAATTGTGTGTTTTTAGCAGAGACGGGGTTTCACCATATTGG A G FEM1A Ensembl:ENSG00000141965 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1320865734 Functional Loss SNV dbSNP153 33..33 33 - - - 23933 RMVar_ID_23933 Human_SNP_ID_656548288 A-to-I Human chr19 - 4820164 4820164 4820164 TGCCCGCCTCAGCCTCCCAAAGTGCTGGGATTATAGGCGTGAGCCACTGCGCCTGGCCCAAACTT TGCCCGCCTCAGCCTCCCAAAGTGCTGGGATTGTAGGCGTGAGCCACTGCGCCTGGCCCAAACTT T C TICAM1 Ensembl:ENSG00000127666 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879833400 Functional Loss SNV dbSNP153 33..33 33 - - - 23934 RMVar_ID_23934 Human_SNP_ID_656548315 A-to-I Human chr19 - 4820234 4820234 4820234 TTGTATTTTTAGTAGAGACGGGGTTTCACCATATTGGCCAGGCTGGTCTCGACCTCCTGATCTCG TTGTATTTTTAGTAGAGACGGGGTTTCACCATTTTGGCCAGGCTGGTCTCGACCTCCTGATCTCG T A TICAM1 Ensembl:ENSG00000127666 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1038909133 Functional Loss SNV dbSNP153 33..33 33 - - - 23935 RMVar_ID_23935 Human_SNP_ID_656548316 A-to-I Human chr19 - 4820234 4820234 4820234 TTGTATTTTTAGTAGAGACGGGGTTTCACCATATTGGCCAGGCTGGTCTCGACCTCCTGATCTCG TTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGGTCTCGACCTCCTGATCTCG T C TICAM1 Ensembl:ENSG00000127666 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1038909133 Functional Loss SNV dbSNP153 33..33 33 - - - 23936 RMVar_ID_23936 Human_SNP_ID_656548529 A-to-I Human chr19 - 4820975 4820975 4820975 GTTGACCAGGCTGATCTTGAACTCATGACCTCAAATGATCTGTCCGCCTTAGCTTCCCAAAGTGC GTTGACCAGGCTGATCTTGAACTCATGACCTCTAATGATCTGTCCGCCTTAGCTTCCCAAAGTGC T A TICAM1 Ensembl:ENSG00000127666 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1308025218 Functional Loss SNV dbSNP153 33..33 33 - - - 23937 RMVar_ID_23937 Human_SNP_ID_656548938 A-to-I Human chr19 - 4822305 4822305 4822305 CTGGGAGGTGGAGGTTGCAGTGAGCCAAGATCATGCCACTGCACTGCAGCCTGGGCGACAGAGCG CTGGGAGGTGGAGGTTGCAGTGAGCCAAGATCGTGCCACTGCACTGCAGCCTGGGCGACAGAGCG T C TICAM1 Ensembl:ENSG00000127666 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs545313637 Functional Loss SNV dbSNP153 33..33 33 - - - 23938 RMVar_ID_23938 Human_SNP_ID_656549265 A-to-I Human chr19 - 4823523 4823523 4823523 TCAACCAATCCTCCCACCTCAGCCTCCTGAGTAGCTGGGATTTCAGGCGCATGCCACCATGCCTG TCAACCAATCCTCCCACCTCAGCCTCCTGAGTCGCTGGGATTTCAGGCGCATGCCACCATGCCTG T G TICAM1 Ensembl:ENSG00000127666 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1568366781 Functional Loss SNV dbSNP153 33..33 33 - - - 23939 RMVar_ID_23939 Human_SNP_ID_656549530 A-to-I Human chr19 - 4824562 4824562 4824562 GGGAGGCCGAGGCAGGTGGGTCATCTGAGGTCAGGGGTTCCAGACCAGCCCGACCAATATGAGGC GGGAGGCCGAGGCAGGTGGGTCATCTGAGGTCGGGGGTTCCAGACCAGCCCGACCAATATGAGGC T C TICAM1 Ensembl:ENSG00000127666 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs918559050 Functional Loss SNV dbSNP153 33..33 33 - - - 23940 RMVar_ID_23940 Human_SNP_ID_656549572 A-to-I Human chr19 - 4824785 4824785 4824785 GGGACTACAGGCACCCGCCACCACACGTGGCTAATTTTTCTATTTTTAGTAGAGACGGGATTTCG GGGACTACAGGCACCCGCCACCACACGTGGCTGATTTTTCTATTTTTAGTAGAGACGGGATTTCG T C TICAM1 Ensembl:ENSG00000127666 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs185115030 Functional Loss SNV dbSNP153 33..33 33 - - - 23941 RMVar_ID_23941 Human_SNP_ID_656549653 A-to-I Human chr19 - 4825088 4825088 4825088 TTTAGTAGAAACGGGGTTTTACCATGTTGCGCAGGCTGGTCTCGAACTCCTGAGCTCAGGCAATC TTTAGTAGAAACGGGGTTTTACCATGTTGCGCGGGCTGGTCTCGAACTCCTGAGCTCAGGCAATC T C TICAM1 Ensembl:ENSG00000127666 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1444086040 Functional Loss SNV dbSNP153 33..33 33 - - - 23942 RMVar_ID_23942 Human_SNP_ID_656549764 A-to-I Human chr19 - 4825485 4825485 4825485 CGGCCGCGGTGGCTCACGCCTGTAATCCCAACACTTTGGGAGGCCAAGGTGGGAGGATCACTTGA CGGCCGCGGTGGCTCACGCCTGTAATCCCAACGCTTTGGGAGGCCAAGGTGGGAGGATCACTTGA T C TICAM1 Ensembl:ENSG00000127666 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs754274371 Functional Loss SNV dbSNP153 33..33 33 - - - 23943 RMVar_ID_23943 Human_SNP_ID_656549805 A-to-I Human chr19 - 4825668 4825661 4825669 CAGGCGTGAGCCACCACACCCGGCCTATTTTTATTTTTTGTAGAGATGGGTCTCACTGTTGCCCA CAGGCGTGAGCCACCACACCCGGCCTATTTT________GTAGAGATGGGTCTCACTGTTGCCCA CAAAAAATA C TICAM1 Ensembl:ENSG00000127666 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1291284575 Functional Loss DEL dbSNP153 32..39 33 - - - 23944 RMVar_ID_23944 Human_SNP_ID_656549834 A-to-I Human chr19 - 4825792 4825792 4825792 ACCATGCCCTGCTAATATTTTTTATTTTTAGTAGAGACAGGGTTTCACTGTGTTGGCTAGGCTGG ACCATGCCCTGCTAATATTTTTTATTTTTAGTGGAGACAGGGTTTCACTGTGTTGGCTAGGCTGG T C TICAM1 Ensembl:ENSG00000127666 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1020546607 Functional Loss SNV dbSNP153 33..33 33 - - - 23945 RMVar_ID_23945 Human_SNP_ID_656549997 A-to-I Human chr19 - 4826435 4826435 4826435 CTGTAGTCCCAGCTACCCGGAAGGCTGAGGCAAGAGAATCGCTTGAACCTGGGAGGCAGAGGTTG CTGTAGTCCCAGCTACCCGGAAGGCTGAGGCATGAGAATCGCTTGAACCTGGGAGGCAGAGGTTG T A TICAM1 Ensembl:ENSG00000127666 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs904708847 Functional Loss SNV dbSNP153 33..33 33 - - - 23946 RMVar_ID_23946 Human_SNP_ID_656550400 A-to-I Human chr19 - 4827671 4827667 4827672 TCGCTGCAAGCTCCGCCTCCCAGGTTCACACCATTCTCCTGCCTCAGCCTTCCGAGTAGCTGGGA TCGCTGCAAGCTCCGCCTCCCAGGTTCACAC_____TCCTGCCTCAGCCTTCCGAGTAGCTGGGA AGAATG A TICAM1 Ensembl:ENSG00000127666 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1453743023 Functional Loss DEL dbSNP153 32..36 33 - - - 23947 RMVar_ID_23947 Human_SNP_ID_656550402 A-to-I Human chr19 - 4827682 4827682 4827682 ACCAACTCGGCTCGCTGCAAGCTCCGCCTCCCAGGTTCACACCATTCTCCTGCCTCAGCCTTCCG ACCAACTCGGCTCGCTGCAAGCTCCGCCTCCCGGGTTCACACCATTCTCCTGCCTCAGCCTTCCG T C TICAM1 Ensembl:ENSG00000127666 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1190277853 Functional Loss SNV dbSNP153 33..33 33 - - - 23948 RMVar_ID_23948 Human_SNP_ID_656550732 A-to-I Human chr19 - 4828841 4828841 4828841 AAAATTACCTGGGCATGGTGGCATGCACCTGTAGTCCCAGCTACTCGGGAGGGTGAGGCAGGAGA AAAATTACCTGGGCATGGTGGCATGCACCTGTCGTCCCAGCTACTCGGGAGGGTGAGGCAGGAGA T G TICAM1 Ensembl:ENSG00000127666 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1028147301 Functional Loss SNV dbSNP153 33..33 33 - - - 23949 RMVar_ID_23949 Human_SNP_ID_656551153 A-to-I Human chr19 - 4830344 4830344 4830344 GCCGGGTGCAGTGGTTTATGCCTGTAATCCCAACACTTTGGGAGGCTGAGGCAGGTGGATTGCTT GCCGGGTGCAGTGGTTTATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGTGGATTGCTT T C TICAM1 Ensembl:ENSG00000127666 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs781403243 Functional Loss SNV dbSNP153 33..33 33 - - - 23950 RMVar_ID_23950 Human_SNP_ID_656553557 A-to-I Human chr19 - 4838733 4838733 4838733 CTACTAAAAATACAAAAAAAAATGAGCCGGGCATGGTAGCAGGTGTCTGTTATCCCAGTTAGGAG CTACTAAAAATACAAAAAAAAATGAGCCGGGCTTGGTAGCAGGTGTCTGTTATCCCAGTTAGGAG T A PLIN3 Ensembl:ENSG00000105355 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1003165944 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8197459,Human_RBP_ID_26471841 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 23951 RMVar_ID_23951 Human_SNP_ID_656556231 A-to-I Human chr19 - 4846616 4846616 4846616 CAGATCACTGCAACCTCCACTTCCCGGGTTCAAGTGATTCTTGGGCCTCCACGTCCCGAGTAGCT CAGATCACTGCAACCTCCACTTCCCGGGTTCAGGTGATTCTTGGGCCTCCACGTCCCGAGTAGCT T C PLIN3 Ensembl:ENSG00000105355 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1439931016 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92029,RMVar_hsa_circ_100935,RMVar_hsa_circ_81635,RMVar_hsa_circ_191600,RMVar_hsa_circ_191599,RMVar_hsa_circ_320477,RMVar_hsa_circ_191603 23952 RMVar_ID_23952 Human_SNP_ID_656559426 A-to-I Human chr19 - 4857216 4857216 4857216 CCAGGCCGGTCTCCAACTCTTGGGCTCAAGCAATCCTCCTGCCTCAGCCCCACAAAGTGCTAGAA CCAGGCCGGTCTCCAACTCTTGGGCTCAAGCAGTCCTCCTGCCTCAGCCCCACAAAGTGCTAGAA T C PLIN3 Ensembl:ENSG00000105355 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs954117041 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92029,RMVar_hsa_circ_81635,RMVar_hsa_circ_191599,RMVar_hsa_circ_191603,RMVar_hsa_circ_375216,RMVar_hsa_circ_191605 23953 RMVar_ID_23953 Human_SNP_ID_656560037 A-to-I Human chr19 - 4858939 4858939 4858939 CCAGCACTTTGGGAGGCCAAGGCGGGAGGATCACCTGAGGTTGGGAGTTTGAGACCAGCCTGACC CCAGCACTTTGGGAGGCCAAGGCGGGAGGATCGCCTGAGGTTGGGAGTTTGAGACCAGCCTGACC T C PLIN3 Ensembl:ENSG00000105355 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1415688554 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92029,RMVar_hsa_circ_81635,RMVar_hsa_circ_191599,RMVar_hsa_circ_191603,RMVar_hsa_circ_375216,RMVar_hsa_circ_191605 23954 RMVar_ID_23954 Human_SNP_ID_656560039 A-to-I Human chr19 - 4858945 4858945 4858945 GTAATCCCAGCACTTTGGGAGGCCAAGGCGGGAGGATCACCTGAGGTTGGGAGTTTGAGACCAGC GTAATCCCAGCACTTTGGGAGGCCAAGGCGGGCGGATCACCTGAGGTTGGGAGTTTGAGACCAGC T G PLIN3 Ensembl:ENSG00000105355 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1470586985 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92029,RMVar_hsa_circ_81635,RMVar_hsa_circ_191599,RMVar_hsa_circ_191603,RMVar_hsa_circ_375216,RMVar_hsa_circ_191605 23955 RMVar_ID_23955 Human_SNP_ID_656560044 A-to-I Human chr19 - 4858953 4858953 4858953 TCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGAGGATCACCTGAGGTTGGGAGTTTG TCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGAGGATCACCTGAGGTTGGGAGTTTG T C PLIN3 Ensembl:ENSG00000105355 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1306226195 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92029,RMVar_hsa_circ_81635,RMVar_hsa_circ_191599,RMVar_hsa_circ_191603,RMVar_hsa_circ_375216,RMVar_hsa_circ_191605 23956 RMVar_ID_23956 Human_SNP_ID_656560708 A-to-I Human chr19 - 4860727 4860727 4860727 ACCCAAAGTGACCCACCCGCCTCGGTCTCCCAAAGTGCTCGGATTACAGGCGTGAGCCACTGCTC ACCCAAAGTGACCCACCCGCCTCGGTCTCCCAGAGTGCTCGGATTACAGGCGTGAGCCACTGCTC T C PLIN3 Ensembl:ENSG00000105355 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1244945776 Functional Loss SNV dbSNP153 33..33 33 - - - 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 23957 RMVar_ID_23957 Human_SNP_ID_656560722 A-to-I Human chr19 - 4860774 4860774 4860774 TAGAGACGGAGTTTCACCATGTTGGCCAGGCTAGTCTCAAACTCCTGACCCAAAGTGACCCACCC TAGAGACGGAGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTCCTGACCCAAAGTGACCCACCC T C PLIN3 Ensembl:ENSG00000105355 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs547219302 Functional Loss SNV dbSNP153 33..33 33 - - - 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 23958 RMVar_ID_23958 Human_SNP_ID_656562102 A-to-I Human chr19 - 4865018 4865018 4865018 CCGCACCTAATTTTTGTATTTTTAGTAGAGACAGTGTTTCAGTATGTTGGCCAGGCTGCTCTTGA CCGCACCTAATTTTTGTATTTTTAGTAGAGACGGTGTTTCAGTATGTTGGCCAGGCTGCTCTTGA T C PLIN3 Ensembl:ENSG00000105355 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs545492906 Functional Loss SNV dbSNP153 33..33 33 - - - 23959 RMVar_ID_23959 Human_SNP_ID_656562103 A-to-I Human chr19 - 4865018 4865018 4865018 CCGCACCTAATTTTTGTATTTTTAGTAGAGACAGTGTTTCAGTATGTTGGCCAGGCTGCTCTTGA CCGCACCTAATTTTTGTATTTTTAGTAGAGACCGTGTTTCAGTATGTTGGCCAGGCTGCTCTTGA T G PLIN3 Ensembl:ENSG00000105355 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs545492906 Functional Loss SNV dbSNP153 33..33 33 - - - 23960 RMVar_ID_23960 Human_SNP_ID_656562204 A-to-I Human chr19 - 4865377 4865377 4865377 TCAAGCAATTCTCCTGCCTCAGCCTCCTGTGTAGCTGGGACTACAGGTGTCAGCCAAAATACACG TCAAGCAATTCTCCTGCCTCAGCCTCCTGTGTGGCTGGGACTACAGGTGTCAGCCAAAATACACG T C PLIN3 Ensembl:ENSG00000105355 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1455257183 Functional Loss SNV dbSNP153 33..33 33 - - - 23961 RMVar_ID_23961 Human_SNP_ID_656578231 A-to-I Human chr19 + 4915566 4915566 4915566 GAAACCCCGTCTCTACTAAAAATACAAAAATTAGCCAGACGTGGTGGCGCATGTCTGTAGTTCCA GAAACCCCGTCTCTACTAAAAATACAAAAATTGGCCAGACGTGGTGGCGCATGTCTGTAGTTCCA A G UHRF1 Ensembl:ENSG00000276043 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs938069138 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80726,RMVar_hsa_circ_191607 23962 RMVar_ID_23962 Human_SNP_ID_656578244 A-to-I Human chr19 + 4915592 4915592 4915592 AAAATTAGCCAGACGTGGTGGCGCATGTCTGTAGTTCCACTTAGGAGGCTGAGGCAGGAGAATCG AAAATTAGCCAGACGTGGTGGCGCATGTCTGTGGTTCCACTTAGGAGGCTGAGGCAGGAGAATCG A G UHRF1 Ensembl:ENSG00000276043 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1438852925 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80726,RMVar_hsa_circ_191607 23963 RMVar_ID_23963 Human_SNP_ID_656579232 A-to-I Human chr19 + 4918442 4918441 4918443 CTGTGCCTGGCCTGTTTTTTTTTTTTTGAGACAGAGTCTTGCTCTGTCGCCAGGCTGGAGTGCGT CTGTGCCTGGCCTGTTTTTTTTTTTTTGAGAC__AGTCTTGCTCTGTCGCCAGGCTGGAGTGCGT CAG C UHRF1 Ensembl:ENSG00000276043 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444438907 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_80726,RMVar_hsa_circ_191607 23964 RMVar_ID_23964 Human_SNP_ID_656581601 A-to-I Human chr19 + 4926572 4926572 4926572 TGGTGGATCGCTTGCTTGAGCCCCGGAGTTCAAAACCAGCTTGGGCAAAGCAGCAAGACCTCATC TGGTGGATCGCTTGCTTGAGCCCCGGAGTTCAGAACCAGCTTGGGCAAAGCAGCAAGACCTCATC A G UHRF1 Ensembl:ENSG00000276043 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs954261694 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80726,RMVar_hsa_circ_191607 23965 RMVar_ID_23965 Human_SNP_ID_656581823 A-to-I Human chr19 + 4927257 4927257 4927257 CAAAAATTAGCTGGGTGTGATGGCTCATGCCTATAGTCCCAAGCTACTCAGGAGGCTGAGGCACA CAAAAATTAGCTGGGTGTGATGGCTCATGCCTTTAGTCCCAAGCTACTCAGGAGGCTGAGGCACA A T UHRF1 Ensembl:ENSG00000276043 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1397683052 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80726,RMVar_hsa_circ_191607 23966 RMVar_ID_23966 Human_SNP_ID_656584381 A-to-I Human chr19 + 4935113 4935113 4935113 CTCCTGCCTCACCCTCCTGAGTAGCTGGGACTATAGGTGCCCACCACCAGCTAATTTTTGTATTT CTCCTGCCTCACCCTCCTGAGTAGCTGGGACTGTAGGTGCCCACCACCAGCTAATTTTTGTATTT A G UHRF1 Ensembl:ENSG00000276043 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs746443089 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80726,RMVar_hsa_circ_21247,RMVar_hsa_circ_191607,RMVar_hsa_circ_88811,RMVar_hsa_circ_17942,RMVar_hsa_circ_191611 23967 RMVar_ID_23967 Human_SNP_ID_656585134 A-to-I Human chr19 + 4937521 4937521 4937521 GTAGCTGGGATTACAGGTGCGTATGCCAGCACACCCAGCTTATTTTTGTATTTTTAGTAGAGGTG GTAGCTGGGATTACAGGTGCGTATGCCAGCACGCCCAGCTTATTTTTGTATTTTTAGTAGAGGTG A G UHRF1 Ensembl:ENSG00000276043 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1293618329 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80726,RMVar_hsa_circ_21247,RMVar_hsa_circ_191607,RMVar_hsa_circ_88811,RMVar_hsa_circ_17942,RMVar_hsa_circ_191611 23968 RMVar_ID_23968 Human_SNP_ID_656585287 A-to-I Human chr19 + 4938060 4938060 4938060 CCTGCAGCCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGTTTGAACCTGGGAGGTGGAGGTT CCTGCAGCCCCAGCTACTTGGGAGGCTGAGGCCGGAGAATCGTTTGAACCTGGGAGGTGGAGGTT A C UHRF1 Ensembl:ENSG00000276043 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1481878814 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80726,RMVar_hsa_circ_21247,RMVar_hsa_circ_191607,RMVar_hsa_circ_88811,RMVar_hsa_circ_17942,RMVar_hsa_circ_191611 23969 RMVar_ID_23969 Human_SNP_ID_656585289 A-to-I Human chr19 + 4938065 4938065 4938065 AGCCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGTTTGAACCTGGGAGGTGGAGGTTGCAGT AGCCCCAGCTACTTGGGAGGCTGAGGCAGGAGGATCGTTTGAACCTGGGAGGTGGAGGTTGCAGT A G UHRF1 Ensembl:ENSG00000276043 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1013658270 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80726,RMVar_hsa_circ_21247,RMVar_hsa_circ_191607,RMVar_hsa_circ_88811,RMVar_hsa_circ_17942,RMVar_hsa_circ_191611 23970 RMVar_ID_23970 Human_SNP_ID_656585771 A-to-I Human chr19 + 4939428 4939428 4939428 GGAGTCTTGCTGTTTGCTGTCTCACCTAGGCTAGAGTGCAGTGGTGCAATCATAGCTCACTGCAG GGAGTCTTGCTGTTTGCTGTCTCACCTAGGCTGGAGTGCAGTGGTGCAATCATAGCTCACTGCAG A G UHRF1 Ensembl:ENSG00000276043 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1235455406 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13493046 RMVar_hsa_circ_80726,RMVar_hsa_circ_21247,RMVar_hsa_circ_191607,RMVar_hsa_circ_88811,RMVar_hsa_circ_17942,RMVar_hsa_circ_191611 23971 RMVar_ID_23971 Human_SNP_ID_656587021 A-to-I Human chr19 + 4942523 4942523 4942523 TGAGACGGAGTCTAATGGCACGATCTTGGCTCACTGCAACCTCTGCCTCCCGGGTTCAAGCAATT TGAGACGGAGTCTAATGGCACGATCTTGGCTCGCTGCAACCTCTGCCTCCCGGGTTCAAGCAATT A G UHRF1 Ensembl:ENSG00000276043 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs576704801 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80726,RMVar_hsa_circ_21247,RMVar_hsa_circ_191607,RMVar_hsa_circ_88811,RMVar_hsa_circ_191613,RMVar_hsa_circ_17942,RMVar_hsa_circ_191611,RMVar_hsa_circ_112377,RMVar_hsa_circ_326319,RMVar_hsa_circ_343449,RMVar_hsa_circ_191614 23972 RMVar_ID_23972 Human_SNP_ID_656588869 A-to-I Human chr19 + 4948019 4948019 4948019 ACAGCTAGTCAGGAGGCTGAGGCAGGAGGATCACTTGAGCCCAGGAGGTTGAGGCCGCAGTGGGC ACAGCTAGTCAGGAGGCTGAGGCAGGAGGATCGCTTGAGCCCAGGAGGTTGAGGCCGCAGTGGGC A G UHRF1 Ensembl:ENSG00000276043 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs936117008 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80726,RMVar_hsa_circ_191607,RMVar_hsa_circ_88811,RMVar_hsa_circ_17942,RMVar_hsa_circ_191611,RMVar_hsa_circ_326319,RMVar_hsa_circ_49733,RMVar_hsa_circ_4378 23973 RMVar_ID_23973 Human_SNP_ID_656593924 A-to-I Human chr19 + 4964282 4964282 4964282 AAAAAAAAAAAAAGTCTTTGATTCAAGATCTCACTTTGTCACCCAGGCTGGAGTACAGTGGTGGT AAAAAAAAAAAAAGTCTTTGATTCAAGATCTCGCTTTGTCACCCAGGCTGGAGTACAGTGGTGGT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031091307 Functional Loss SNV dbSNP153 33..33 33 - - - 23974 RMVar_ID_23974 Human_SNP_ID_656635147 A-to-I Human chr19 + 5100463 5100462 5100464 CTTCAAGACAGGATCTCACTCTGAAATGAGACAGAGTCTCAGCCTAGAGTGCAGTGGTGCAGTCA CTTCAAGACAGGATCTCACTCTGAAATGAGAC__AGTCTCAGCCTAGAGTGCAGTGGTGCAGTCA CAG C KDM4B Ensembl:ENSG00000127663 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs776253721 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_13500203 RMVar_hsa_circ_8177,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_103299,RMVar_hsa_circ_191630,RMVar_hsa_circ_123207,RMVar_hsa_circ_78325,RMVar_hsa_circ_191644,RMVar_hsa_circ_191631,RMVar_hsa_circ_116647,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_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_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_105477,RMVar_hsa_circ_191656,RMVar_hsa_circ_69307,RMVar_hsa_circ_191655,RMVar_hsa_circ_58574,RMVar_hsa_circ_191653,RMVar_hsa_circ_269053 23975 RMVar_ID_23975 Human_SNP_ID_656650068 A-to-I Human chr19 + 5147622 5147622 5147622 AAAATTAGCTGGGCATGGTGGCACGCACCTTTAGTCCCAGCTACTTGGGAAGCTGAGGTGGGAGG AAAATTAGCTGGGCATGGTGGCACGCACCTTTTGTCCCAGCTACTTGGGAAGCTGAGGTGGGAGG A T KDM4B Ensembl:ENSG00000127663 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1365506486 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117265,RMVar_hsa_circ_191639,RMVar_hsa_circ_121383,RMVar_hsa_circ_125046,RMVar_hsa_circ_191652,RMVar_hsa_circ_68757,RMVar_hsa_circ_191653,RMVar_hsa_circ_57373,RMVar_hsa_circ_26368 23976 RMVar_ID_23976 Human_SNP_ID_656674432 A-to-I Human chr19 - 5226741 5226740 5226742 GTTTATACAGTTTATTTATTTATTTTTGAGACAGTCTTGCTCTGTCACCCAGGCTGGAGTACAGT GTTTATACAGTTTATTTATTTATTTTTGAGA__GTCTTGCTCTGTCACCCAGGCTGGAGTACAGT CTG C PTPRS Ensembl:ENSG00000105426 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879796187 Functional Loss DEL dbSNP153 32..33 33 - - - 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 23977 RMVar_ID_23977 Human_SNP_ID_656691877 A-to-I Human chr19 - 5281422 5281422 5281422 GAGTCTTGCCCTGTCCCCCAGGCTGGAGTGCAATGGCGTGATCTCAGCTCACTGCAACCTCTGCC GAGTCTTGCCCTGTCCCCCAGGCTGGAGTGCAGTGGCGTGATCTCAGCTCACTGCAACCTCTGCC T C PTPRS Ensembl:ENSG00000105426 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560683548 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111781,RMVar_hsa_circ_191665,RMVar_hsa_circ_191677,RMVar_hsa_circ_116193,RMVar_hsa_circ_14747,RMVar_hsa_circ_97862,RMVar_hsa_circ_191697,RMVar_hsa_circ_46836 23978 RMVar_ID_23978 Human_SNP_ID_656780741 A-to-I Human chr19 - 5596119 5596119 5596119 AGCTGGGATTACAGGCATGCGCCACCACGCCTAGCTAATTTTTGTATTTTTAGTTGAGACGGGGT AGCTGGGATTACAGGCATGCGCCACCACGCCTGGCTAATTTTTGTATTTTTAGTTGAGACGGGGT T C SAFB2 Ensembl:ENSG00000130254 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs938703385 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25433879 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_18988,RMVar_hsa_circ_116787,RMVar_hsa_circ_191704 23979 RMVar_ID_23979 Human_SNP_ID_656784340 A-to-I Human chr19 - 5609005 5609005 5609005 CTCTGTTGCCCAGGCTGAAGTGCAGTGGTGTGATCTTGGCTCACTGCAGCCTCCGCCTCCCTCCC CTCTGTTGCCCAGGCTGAAGTGCAGTGGTGTGGTCTTGGCTCACTGCAGCCTCCGCCTCCCTCCC T C SAFB2 Ensembl:ENSG00000130254 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1291019673 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81595,RMVar_hsa_circ_87448,RMVar_hsa_circ_119906,RMVar_hsa_circ_191701,RMVar_hsa_circ_191702,RMVar_hsa_circ_116484,RMVar_hsa_circ_116787,RMVar_hsa_circ_191704,RMVar_hsa_circ_358881,RMVar_hsa_circ_306795,RMVar_hsa_circ_123874,RMVar_hsa_circ_110738,RMVar_hsa_circ_85525,RMVar_hsa_circ_191711,RMVar_hsa_circ_191713,RMVar_hsa_circ_80099,RMVar_hsa_circ_191714,RMVar_hsa_circ_191712,RMVar_hsa_circ_191709,RMVar_hsa_circ_191710,RMVar_hsa_circ_191708,RMVar_hsa_circ_265316 23980 RMVar_ID_23980 Human_SNP_ID_656784666 A-to-I Human chr19 - 5609913 5609913 5609913 GGAAGCTCTGCTGGGCACGGTGGTTCACGTCTATAATCCCAGCAGTTTGGGAGGCTGAGGCAGGA GGAAGCTCTGCTGGGCACGGTGGTTCACGTCTGTAATCCCAGCAGTTTGGGAGGCTGAGGCAGGA T C SAFB2 Ensembl:ENSG00000130254 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1442587473 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81595,RMVar_hsa_circ_87448,RMVar_hsa_circ_119906,RMVar_hsa_circ_191701,RMVar_hsa_circ_191702,RMVar_hsa_circ_116484,RMVar_hsa_circ_116787,RMVar_hsa_circ_191704,RMVar_hsa_circ_358881,RMVar_hsa_circ_306795,RMVar_hsa_circ_123874,RMVar_hsa_circ_110738,RMVar_hsa_circ_85525,RMVar_hsa_circ_191711,RMVar_hsa_circ_191713,RMVar_hsa_circ_80099,RMVar_hsa_circ_191714,RMVar_hsa_circ_191712,RMVar_hsa_circ_191709,RMVar_hsa_circ_191710,RMVar_hsa_circ_191708,RMVar_hsa_circ_265316 23981 RMVar_ID_23981 Human_SNP_ID_656786150 A-to-I Human chr19 - 5615349 5615348 5615350 TTGTGTTTTGTTTGTTTGTTTGTTTTTGAGACAGAGTCTCTCTCAGTCACCCAGGCTGGAGTGCA TTGTGTTTTGTTTGTTTGTTTGTTTTTGAGA__GAGTCTCTCTCAGTCACCCAGGCTGGAGTGCA CTG C SAFB2 Ensembl:ENSG00000130254 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1292765060 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_81595,RMVar_hsa_circ_87448,RMVar_hsa_circ_191702,RMVar_hsa_circ_116484,RMVar_hsa_circ_116787,RMVar_hsa_circ_191704,RMVar_hsa_circ_306795,RMVar_hsa_circ_123874,RMVar_hsa_circ_191711,RMVar_hsa_circ_191713,RMVar_hsa_circ_191714,RMVar_hsa_circ_191712,RMVar_hsa_circ_12056,RMVar_hsa_circ_191715 23982 RMVar_ID_23982 Human_SNP_ID_656797730 A-to-I Human chr19 + 5655379 5655379 5655379 ACTCAAAAGGCTGAGGTGGGAGAATGCCACTTAAACCTGGGAGGTCAAGACTGTAGTGAGCCACG ACTCAAAAGGCTGAGGTGGGAGAATGCCACTTGAACCTGGGAGGTCAAGACTGTAGTGAGCCACG A G SAFB Ensembl:ENSG00000160633 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs918256251 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2570689,Human_RBP_ID_13513643 RMVar_hsa_circ_359003,RMVar_hsa_circ_65883,RMVar_hsa_circ_72641,RMVar_hsa_circ_331764,RMVar_hsa_circ_271748,RMVar_hsa_circ_191726,RMVar_hsa_circ_35510,RMVar_hsa_circ_191727,RMVar_hsa_circ_191728 23983 RMVar_ID_23983 Human_SNP_ID_656797731 A-to-I Human chr19 + 5655380 5655380 5655380 CTCAAAAGGCTGAGGTGGGAGAATGCCACTTAAACCTGGGAGGTCAAGACTGTAGTGAGCCACGT CTCAAAAGGCTGAGGTGGGAGAATGCCACTTATACCTGGGAGGTCAAGACTGTAGTGAGCCACGT A T SAFB Ensembl:ENSG00000160633 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs929747685 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2570689,Human_RBP_ID_13513643 RMVar_hsa_circ_359003,RMVar_hsa_circ_65883,RMVar_hsa_circ_72641,RMVar_hsa_circ_331764,RMVar_hsa_circ_271748,RMVar_hsa_circ_191726,RMVar_hsa_circ_35510,RMVar_hsa_circ_191727,RMVar_hsa_circ_191728 23984 RMVar_ID_23984 Human_SNP_ID_656797750 A-to-I Human chr19 + 5655444 5655444 5655444 TTCATTGCACTGCACTCTAGCCTGGGAGAGAGAGTGAGACCCCATCTCAAAAAAAAAAAAAAAAA TTCATTGCACTGCACTCTAGCCTGGGAGAGAGTGTGAGACCCCATCTCAAAAAAAAAAAAAAAAA A T SAFB Ensembl:ENSG00000160633 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs937693129 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13513643 RMVar_hsa_circ_359003,RMVar_hsa_circ_65883,RMVar_hsa_circ_72641,RMVar_hsa_circ_331764,RMVar_hsa_circ_271748,RMVar_hsa_circ_191726,RMVar_hsa_circ_35510,RMVar_hsa_circ_191727,RMVar_hsa_circ_191728 23985 RMVar_ID_23985 Human_SNP_ID_656798451 A-to-I Human chr19 + 5657705 5657705 5657705 CGCCACCACACCTGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCTAGGC CGCCACCACACCTGGCTAATTTTTGTATTTTTTGTAGAGACGGGGTTTCACCATGTTGGCTAGGC A T SAFB Ensembl:ENSG00000160633 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1415322585 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35510,RMVar_hsa_circ_191727 23986 RMVar_ID_23986 Human_SNP_ID_656798483 A-to-I Human chr19 + 5657799 5657798 5657800 CACCTGCCTTGGCCTCCCAAAGTGCCAGGATTACAGACGTGAGCCACTGCACCCGGCCTACTTAC CACCTGCCTTGGCCTCCCAAAGTGCCAGGATT__AGACGTGAGCCACTGCACCCGGCCTACTTAC TAC T SAFB Ensembl:ENSG00000160633 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1263030254 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_6784994,Human_RBP_ID_13513758,Human_RBP_ID_23309981 RMVar_hsa_circ_35510,RMVar_hsa_circ_191727 23987 RMVar_ID_23987 Human_SNP_ID_656799428 A-to-I Human chr19 + 5660620 5660620 5660620 AAATCTGAGCCTGGGCACAGTGGTTCATGCCTATAATCCCAGCACTTTGGGAGGTGGAGGCGGGC AAATCTGAGCCTGGGCACAGTGGTTCATGCCTGTAATCCCAGCACTTTGGGAGGTGGAGGCGGGC A G SAFB Ensembl:ENSG00000160633 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1005749645 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13513923 RMVar_hsa_circ_35510,RMVar_hsa_circ_191727 23988 RMVar_ID_23988 Human_SNP_ID_656799975 A-to-I Human chr19 + 5661964 5661964 5661964 TGGAGTGCAGTGACCCGATCTTGGCTCACTGCAAGCTCTGCCTCCCGGGTTCACACCATTCTCCT TGGAGTGCAGTGACCCGATCTTGGCTCACTGCTAGCTCTGCCTCCCGGGTTCACACCATTCTCCT A T SAFB Ensembl:ENSG00000160633 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1411576015 Functional Loss SNV dbSNP153 33..33 33 - - - 23989 RMVar_ID_23989 Human_SNP_ID_656800079 A-to-I Human chr19 + 5662242 5662242 5662242 AGCATAGGCCGGGTGCGCTAGTTCACGCCTGTAATCCTAACATTTTGGGAGGCCAGGGTGGGCGG AGCATAGGCCGGGTGCGCTAGTTCACGCCTGTCATCCTAACATTTTGGGAGGCCAGGGTGGGCGG A C SAFB Ensembl:ENSG00000160633 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs987563725 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17567881 23990 RMVar_ID_23990 Human_SNP_ID_656800144 A-to-I Human chr19 + 5662426 5662426 5662426 TGAGGCAGGAAAATCGCGTGTACCCAGGAGGCAGAGGTTGCAGTGAGCCAAGATCGTGCCACTGC TGAGGCAGGAAAATCGCGTGTACCCAGGAGGCCGAGGTTGCAGTGAGCCAAGATCGTGCCACTGC A C SAFB Ensembl:ENSG00000160633 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1042587963 Functional Loss SNV dbSNP153 33..33 33 - - - 23991 RMVar_ID_23991 Human_SNP_ID_656807042 A-to-I Human chr19 + 5685322 5685322 5685322 CTTTCTGGCCAGGCACGGTGGCTCACGCTTGTAGTCAGCACTTTGGGAGGCCGAGGAAAGTGGAT CTTTCTGGCCAGGCACGGTGGCTCACGCTTGTGGTCAGCACTTTGGGAGGCCGAGGAAAGTGGAT A G HSD11B1L,RPL36 Ensembl:ENSG00000167733,Ensembl:ENSG00000130255 Protein coding,Protein coding intron,intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1326003346 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1942684,Human_Splice_Rec_1942698 23992 RMVar_ID_23992 Human_SNP_ID_656809738 A-to-I Human chr19 - 5692102 5692102 5692102 CATCACCGAGGGCCTGGAGGTGCACTTCGTGGAACACTACCGGGAGATCTTCGACATCGCCTTCC CATCACCGAGGGCCTGGAGGTGCACTTCGTGGGACACTACCGGGAGATCTTCGACATCGCCTTCC T C LONP1 Ensembl:ENSG00000196365 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs751799454 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1571688,Human_RBP_ID_1892089,Human_RBP_ID_22503771,Human_RBP_ID_23114712 Human_miRNA_ID_2061756 RMVar_hsa_circ_127193,RMVar_hsa_circ_191738,RMVar_hsa_circ_110522,RMVar_hsa_circ_191737 23993 RMVar_ID_23993 Human_SNP_ID_656812092 A-to-I Human chr19 - 5696710 5696710 5696710 CGCCATGCCCGGGAAGATCATCCAGTGTTTGAAGAAGACCAAGACGGAGAACCCCCTGATCCTCA CGCCATGCCCGGGAAGATCATCCAGTGTTTGAGGAAGACCAAGACGGAGAACCCCCTGATCCTCA T C LONP1 Ensembl:ENSG00000196365 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1302194252 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_303960,Human_RBP_ID_910375,Human_RBP_ID_1892107,Human_RBP_ID_3956077,Human_RBP_ID_9380198,Human_RBP_ID_18412465,Human_RBP_ID_18994141,Human_RBP_ID_24545634,Human_RBP_ID_26334791 Human_Splice_Rec_1942798,Human_Splice_Rec_1942830,Human_Splice_Rec_1942831,Human_Splice_Rec_1942864,Human_Splice_Rec_1942865,Human_Splice_Rec_1942900,Human_Splice_Rec_1942901,Human_Splice_Rec_1942934,Human_Splice_Rec_1942935,Human_Splice_Rec_1942968,Human_Splice_Rec_1942969,Human_Splice_Rec_1943002,Human_Splice_Rec_1943003,Human_Splice_Rec_1943030 Human_miRNA_ID_829387,Human_miRNA_ID_1023707 RMVar_hsa_circ_97269,RMVar_hsa_circ_127193,RMVar_hsa_circ_191738,RMVar_hsa_circ_191739,RMVar_hsa_circ_321950 23994 RMVar_ID_23994 Human_SNP_ID_656816415 A-to-I Human chr19 - 5706248 5706245 5706249 CCTGTGGTCCCAGTTACTCAGGAGGCTAAGGCAGGAGGATCGCTTGAGCCCAGGAGGTGGAGGCT CCTGTGGTCCCAGTTACTCAGGAGGCTAAGG____AGGATCGCTTGAGCCCAGGAGGTGGAGGCT TCCTG T LONP1 Ensembl:ENSG00000196365 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1031312633 Functional Loss DEL dbSNP153 32..35 33 - - - RMVar_hsa_circ_127193,RMVar_hsa_circ_191738,RMVar_hsa_circ_191745,RMVar_hsa_circ_336723,RMVar_hsa_circ_371205,RMVar_hsa_circ_120487,RMVar_hsa_circ_191746,RMVar_hsa_circ_191747,RMVar_hsa_circ_10622,RMVar_hsa_circ_364585,RMVar_hsa_circ_377831,RMVar_hsa_circ_343012,RMVar_hsa_circ_300800,RMVar_hsa_circ_191749,RMVar_hsa_circ_191750,RMVar_hsa_circ_191748 23995 RMVar_ID_23995 Human_SNP_ID_656816419 A-to-I Human chr19 - 5706261 5706261 5706261 GGTGTGGCAGGTGCCTGTGGTCCCAGTTACTCAGGAGGCTAAGGCAGGAGGATCGCTTGAGCCCA GGTGTGGCAGGTGCCTGTGGTCCCAGTTACTCGGGAGGCTAAGGCAGGAGGATCGCTTGAGCCCA T C LONP1 Ensembl:ENSG00000196365 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910414434 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127193,RMVar_hsa_circ_191738,RMVar_hsa_circ_191745,RMVar_hsa_circ_336723,RMVar_hsa_circ_371205,RMVar_hsa_circ_120487,RMVar_hsa_circ_191746,RMVar_hsa_circ_191747,RMVar_hsa_circ_10622,RMVar_hsa_circ_364585,RMVar_hsa_circ_377831,RMVar_hsa_circ_343012,RMVar_hsa_circ_300800,RMVar_hsa_circ_191749,RMVar_hsa_circ_191750,RMVar_hsa_circ_191748 23996 RMVar_ID_23996 Human_SNP_ID_656816493 A-to-I Human chr19 - 5706507 5706507 5706507 CACCTCCAGGGCTCAAGTGATCCTCCCACCTCAGCCTCCCGAGTAGCTGGGATTACAGGCGTGCA CACCTCCAGGGCTCAAGTGATCCTCCCACCTCGGCCTCCCGAGTAGCTGGGATTACAGGCGTGCA T C LONP1 Ensembl:ENSG00000196365 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1336847147 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127193,RMVar_hsa_circ_191738,RMVar_hsa_circ_191745,RMVar_hsa_circ_336723,RMVar_hsa_circ_371205,RMVar_hsa_circ_120487,RMVar_hsa_circ_191746,RMVar_hsa_circ_191747,RMVar_hsa_circ_10622,RMVar_hsa_circ_364585,RMVar_hsa_circ_377831,RMVar_hsa_circ_343012,RMVar_hsa_circ_300800,RMVar_hsa_circ_191749,RMVar_hsa_circ_191750,RMVar_hsa_circ_191748 23997 RMVar_ID_23997 Human_SNP_ID_656817591 A-to-I Human chr19 - 5709230 5709230 5709230 CCTAACTCTGCCTCCCAAAGTGTTGGTGTTACAGGTGTGAGCCACCGCGCCCGGCCAAGACCAGG CCTAACTCTGCCTCCCAAAGTGTTGGTGTTACGGGTGTGAGCCACCGCGCCCGGCCAAGACCAGG T C LONP1 Ensembl:ENSG00000196365 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1001651614 Functional Loss SNV dbSNP153 33..33 33 - - - 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 23998 RMVar_ID_23998 Human_SNP_ID_656817643 A-to-I Human chr19 - 5709418 5709418 5709418 TGGCTCATGGCAACCTCCGCCTCCTGGGTTCAAGTGATTCTCCTGCCTCGGCCTCCTTAGTAGCT TGGCTCATGGCAACCTCCGCCTCCTGGGTTCACGTGATTCTCCTGCCTCGGCCTCCTTAGTAGCT T G LONP1 Ensembl:ENSG00000196365 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1450093158 Functional Loss SNV dbSNP153 33..33 33 - - - 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 23999 RMVar_ID_23999 Human_SNP_ID_656817725 A-to-I Human chr19 - 5709675 5709675 5709675 TGGATCTCCTGACCTCGTGATCCGCCCGCCTTAGCATCCCAAAGTGCTGGGGTTACAGGCGTGAG TGGATCTCCTGACCTCGTGATCCGCCCGCCTTGGCATCCCAAAGTGCTGGGGTTACAGGCGTGAG T C LONP1 Ensembl:ENSG00000196365 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs962514711 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25434966 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 24000 RMVar_ID_24000 Human_SNP_ID_656817749 A-to-I Human chr19 - 5709742 5709742 5709742 ACACCCGGCTAATTTTTTGTGTATTTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGG ACACCCGGCTAATTTTTTGTGTATTTTTTAGTTGAGACGGGGTTTCACCGTGTTAGCCAGGATGG T A LONP1 Ensembl:ENSG00000196365 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs1251912876 Functional Loss SNV dbSNP153 33..33 33 - - - 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 24001 RMVar_ID_24001 Human_SNP_ID_656817768 A-to-I Human chr19 - 5709790 5709790 5709790 CTCCTGCCTCAGCCTCCCCAGTAGCTGGGACTACAGGTGCCCGCCACCACACCCGGCTAATTTTT CTCCTGCCTCAGCCTCCCCAGTAGCTGGGACTGCAGGTGCCCGCCACCACACCCGGCTAATTTTT T C LONP1 Ensembl:ENSG00000196365 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1432853479 Functional Loss SNV dbSNP153 33..33 33 - - - 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 24002 RMVar_ID_24002 Human_SNP_ID_656817953 A-to-I Human chr19 - 5710189 5710189 5710189 TCCCAGCTACTCGGGATTACTGAGGCGGGAGAATTGCTTGAACCTGGGAGGCAGAGGTTGCGGTG TCCCAGCTACTCGGGATTACTGAGGCGGGAGAGTTGCTTGAACCTGGGAGGCAGAGGTTGCGGTG T C LONP1 Ensembl:ENSG00000196365 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs368684745 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17568357,Human_RBP_ID_23309987 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 24003 RMVar_ID_24003 Human_SNP_ID_656817984 A-to-I Human chr19 - 5710267 5710267 5710267 CTGACCAACATGGAGAAACCCCGTGTCTACTAAAAATACAAAAAAAAATTAGCCAGGTGTGGTGG CTGACCAACATGGAGAAACCCCGTGTCTACTACAAATACAAAAAAAAATTAGCCAGGTGTGGTGG T G LONP1 Ensembl:ENSG00000196365 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1351493285 Functional Loss SNV dbSNP153 33..33 33 - - - 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 24004 RMVar_ID_24004 Human_SNP_ID_656818090 A-to-I Human chr19 - 5710644 5710644 5710644 GCTGGGTACAGTGTCTCATGCCTGTCATCCCAACACTTTTGGAGGCCAAGGAAGGAGGATCACTT GCTGGGTACAGTGTCTCATGCCTGTCATCCCAGCACTTTTGGAGGCCAAGGAAGGAGGATCACTT T C LONP1 Ensembl:ENSG00000196365 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1019788095 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13516159,Human_RBP_ID_17567530,Human_RBP_ID_22477073,Human_RBP_ID_23180435,Human_RBP_ID_26995915 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 24005 RMVar_ID_24005 Human_SNP_ID_656818141 A-to-I Human chr19 - 5710829 5710829 5710829 TAGAGACGAGGTTTTACCATGTTGGCCGGGCTAGTCTCAAACTCCTGACCTCGGGTGATCCGCCC TAGAGACGAGGTTTTACCATGTTGGCCGGGCTGGTCTCAAACTCCTGACCTCGGGTGATCCGCCC T C LONP1 Ensembl:ENSG00000196365 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs1032317991 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17568361 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 24006 RMVar_ID_24006 Human_SNP_ID_656818162 A-to-I Human chr19 - 5710913 5710913 5710913 CAAGTGATTCTCATGCCTCAGCCTCCCAAGTAACTGGGATTGCAGGCACGTGCCACCACACACGG CAAGTGATTCTCATGCCTCAGCCTCCCAAGTAGCTGGGATTGCAGGCACGTGCCACCACACACGG T C LONP1 Ensembl:ENSG00000196365 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1289782773 Functional Loss SNV dbSNP153 33..33 33 - - - 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 24007 RMVar_ID_24007 Human_SNP_ID_656818171 A-to-I Human chr19 - 5710957 5710957 5710957 CAATGGAACGATCTCAGCTCACTGCAATTTCCACCTCCCAGGTTCAAGTGATTCTCATGCCTCAG CAATGGAACGATCTCAGCTCACTGCAATTTCCGCCTCCCAGGTTCAAGTGATTCTCATGCCTCAG T C LONP1 Ensembl:ENSG00000196365 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1345924362 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13516190,Human_RBP_ID_25434981 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 24008 RMVar_ID_24008 Human_SNP_ID_656818182 A-to-I Human chr19 - 5710987 5710987 5710987 AGTCTGGCTCTGTCAACCCAGGCTGGAGTGCAATGGAACGATCTCAGCTCACTGCAATTTCCACC AGTCTGGCTCTGTCAACCCAGGCTGGAGTGCAGTGGAACGATCTCAGCTCACTGCAATTTCCACC T C LONP1 Ensembl:ENSG00000196365 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs368877470 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22239676,Human_RBP_ID_22476416,Human_RBP_ID_22976376 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 24009 RMVar_ID_24009 Human_SNP_ID_656819255 A-to-I Human chr19 - 5714365 5714365 5714365 AGTGGGGGTGGAGGTTGCAGTGAGCTGAGATCACGCCATTACATTCCAGCCAGGGCAACAGAATG AGTGGGGGTGGAGGTTGCAGTGAGCTGAGATCGCGCCATTACATTCCAGCCAGGGCAACAGAATG T C LONP1 Ensembl:ENSG00000196365 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1035023682 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127193,RMVar_hsa_circ_191738,RMVar_hsa_circ_120487,RMVar_hsa_circ_191747 24010 RMVar_ID_24010 Human_SNP_ID_656820273 A-to-I Human chr19 - 5716932 5716931 5716932 AAAATTAGCCTGGAGTGGTGGTGGGCGCCCGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTAGCCTGGAGTGGTGGTGGGCGCCCGT_GTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA CT C LONP1 Ensembl:ENSG00000196365 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1244203469 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_127193,RMVar_hsa_circ_191738,RMVar_hsa_circ_120487,RMVar_hsa_circ_191747 24011 RMVar_ID_24011 Human_SNP_ID_656820274 A-to-I Human chr19 - 5716932 5716932 5716932 AAAATTAGCCTGGAGTGGTGGTGGGCGCCCGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTAGCCTGGAGTGGTGGTGGGCGCCCGTTGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA T A LONP1 Ensembl:ENSG00000196365 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1568329678 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127193,RMVar_hsa_circ_191738,RMVar_hsa_circ_120487,RMVar_hsa_circ_191747 24012 RMVar_ID_24012 Human_SNP_ID_656820703 A-to-I Human chr19 - 5718415 5718415 5718415 AAAGTGCAGTGGCGCGATTTCAGCTCACTGCAACCTCTGCCTCCCGGGTTCAAGTGATTCTCCTG AAAGTGCAGTGGCGCGATTTCAGCTCACTGCAGCCTCTGCCTCCCGGGTTCAAGTGATTCTCCTG T C LONP1 Ensembl:ENSG00000196365 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1226160127 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127193,RMVar_hsa_circ_191738,RMVar_hsa_circ_120487,RMVar_hsa_circ_191747 24013 RMVar_ID_24013 Human_SNP_ID_656852680 A-to-I Human chr19 - 5816439 5816439 5816439 GGGAGGCGGAGGTTGCAGCGAGCCGAGACTGCACCACTGCATTCCAGCCTGGACGACAGAGCAAG GGGAGGCGGAGGTTGCAGCGAGCCGAGACTGCGCCACTGCATTCCAGCCTGGACGACAGAGCAAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1307572011 Functional Loss SNV dbSNP153 33..33 33 - - - 24014 RMVar_ID_24014 Human_SNP_ID_656875589 A-to-I Human chr19 - 5893286 5893286 5893286 TAATTGTTTTTATTTTTATTTTTTGTAGAGACAGGATCTCACTGTGTTGTGCAGGCTGGTCTCAA TAATTGTTTTTATTTTTATTTTTTGTAGAGACTGGATCTCACTGTGTTGTGCAGGCTGGTCTCAA T A AC024592.3,NDUFA11 Ensembl:ENSG00000267740,Ensembl:ENSG00000174886 Protein coding,Protein coding intron,CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1002976626 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17567884 Human_Splice_Rec_1943372 24015 RMVar_ID_24015 Human_SNP_ID_656875590 A-to-I Human chr19 - 5893286 5893286 5893286 TAATTGTTTTTATTTTTATTTTTTGTAGAGACAGGATCTCACTGTGTTGTGCAGGCTGGTCTCAA TAATTGTTTTTATTTTTATTTTTTGTAGAGACGGGATCTCACTGTGTTGTGCAGGCTGGTCTCAA T C AC024592.3,NDUFA11 Ensembl:ENSG00000267740,Ensembl:ENSG00000174886 Protein coding,Protein coding intron,CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1002976626 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17567884 Human_Splice_Rec_1943372 24016 RMVar_ID_24016 Human_SNP_ID_656880546 A-to-I Human chr19 + 5909498 5909497 5909498 TGTGAGTTTCTGTTTTTTGTTTTTTTTTTTTTAAGACAGAGTCCCACTCTGTCGCCCTGGCTGGG TGTGAGTTTCTGTTTTTTGTTTTTTTTTTTTT_AGACAGAGTCCCACTCTGTCGCCCTGGCTGGG TA T VMAC,AC104532.1 Ensembl:ENSG00000187650,Ensembl:ENSG00000267314 Protein coding,Protein coding 3'UTR,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs754072859 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_528644,Human_RBP_ID_13542770 RMVar_hsa_circ_191764,RMVar_hsa_circ_128100 24017 RMVar_ID_24017 Human_SNP_ID_656880550 A-to-I Human chr19 + 5909511 5909511 5909511 TTTTTGTTTTTTTTTTTTTAAGACAGAGTCCCACTCTGTCGCCCTGGCTGGGGTGCAGTGGTGCG TTTTTGTTTTTTTTTTTTTAAGACAGAGTCCCTCTCTGTCGCCCTGGCTGGGGTGCAGTGGTGCG A T VMAC,AC104532.1 Ensembl:ENSG00000187650,Ensembl:ENSG00000267314 Protein coding,Protein coding 3'UTR,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1453263971 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_528644,Human_RBP_ID_13542770 RMVar_hsa_circ_191764,RMVar_hsa_circ_128100 24018 RMVar_ID_24018 Human_SNP_ID_656880591 A-to-I Human chr19 + 5909696 5909696 5909696 GACCGGGGAGGGGAGGGGGTTTCACCATGTTGACCAGGCTGGTCTCAAACTCCTGACCTTAGGTG GACCGGGGAGGGGAGGGGGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTCCTGACCTTAGGTG A G VMAC,AC104532.1 Ensembl:ENSG00000187650,Ensembl:ENSG00000267314 Protein coding,Protein coding 3'UTR,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1185722346 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_191764,RMVar_hsa_circ_128100 24019 RMVar_ID_24019 Human_SNP_ID_656880799 A-to-I Human chr19 + 5910487 5910487 5910487 CACTTTGGGATGCGGGTGGATCACCTGAGGTCAGGAGTTCGAGACCACCCTGGCCAACATGGTGA CACTTTGGGATGCGGGTGGATCACCTGAGGTCGGGAGTTCGAGACCACCCTGGCCAACATGGTGA A G VMAC,AC104532.1 Ensembl:ENSG00000187650,Ensembl:ENSG00000267314 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1281164145 Functional Loss SNV dbSNP153 33..33 33 - - - 24020 RMVar_ID_24020 Human_SNP_ID_656880976 A-to-I Human chr19 + 5911011 5911011 5911011 GAGGCCAGGAGTTCAAGACCAGCCTGACCAACATGGTGAAACTCCGTCTCTACTAAAAACACAAA GAGGCCAGGAGTTCAAGACCAGCCTGACCAACGTGGTGAAACTCCGTCTCTACTAAAAACACAAA A G AC104532.1 Ensembl:ENSG00000267314 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215510447 Functional Loss SNV dbSNP153 33..33 33 - - - 24021 RMVar_ID_24021 Human_SNP_ID_656880998 A-to-I Human chr19 + 5911084 5911084 5911084 GGGTGTGGTGGCGCGTGCCTGTAATCCCAGATACTCGGGAGGTTGAGGCAGGAGAATCACTTGAA GGGTGTGGTGGCGCGTGCCTGTAATCCCAGATTCTCGGGAGGTTGAGGCAGGAGAATCACTTGAA A T AC104532.1 Ensembl:ENSG00000267314 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs570238469 Functional Loss SNV dbSNP153 33..33 33 - - - 24022 RMVar_ID_24022 Human_SNP_ID_656881062 A-to-I Human chr19 + 5911305 5911305 5911305 CCTGGCTGCGTTTTTGCATTTTTTCTAGAGATAAGGTCTCATTACATTGCCCAGGCTGGTCTTGA CCTGGCTGCGTTTTTGCATTTTTTCTAGAGATGAGGTCTCATTACATTGCCCAGGCTGGTCTTGA A G AC104532.1 Ensembl:ENSG00000267314 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 29129909,30559470 RNA-Seq:(High) rs141833075 Functional Loss SNV dbSNP153 33..33 33 - - - 24023 RMVar_ID_24023 Human_SNP_ID_656881070 A-to-I Human chr19 + 5911350 5911350 5911350 ATTGCCCAGGCTGGTCTTGAACTCCTGGCCTCAAGTGATCCTCCCGCATTGGCCTCCCAAGAAAT ATTGCCCAGGCTGGTCTTGAACTCCTGGCCTCCAGTGATCCTCCCGCATTGGCCTCCCAAGAAAT A C AC104532.1 Ensembl:ENSG00000267314 Protein coding intron GSE100210;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229 RNA-Seq:(High) rs543807075 Functional Loss SNV dbSNP153 33..33 33 - - - 24024 RMVar_ID_24024 Human_SNP_ID_656881365 A-to-I Human chr19 + 5912425 5912425 5912425 ACCTCAGGTGATCTGTCTGCCTCGGCCTCCCAAAGTGCTGTGATTACAGGCATGAGCCACCGCAC ACCTCAGGTGATCTGTCTGCCTCGGCCTCCCAGAGTGCTGTGATTACAGGCATGAGCCACCGCAC A G CAPS,AC104532.1 Ensembl:ENSG00000105519,Ensembl:ENSG00000267314 Protein coding,Protein coding 5'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1421878993 Functional Loss SNV dbSNP153 33..33 33 - - - 24025 RMVar_ID_24025 Human_SNP_ID_656881475 A-to-I Human chr19 + 5912843 5912843 5912843 GTTGCACAGGCGGGTCTCAAACTCCTGGGCTCAAGTGATCTTCCTGCCCTGGCTTCCCAAAGTGT GTTGCACAGGCGGGTCTCAAACTCCTGGGCTCGAGTGATCTTCCTGCCCTGGCTTCCCAAAGTGT A G CAPS,AC104532.1 Ensembl:ENSG00000105519,Ensembl:ENSG00000267314 Protein coding,Protein coding intron,intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs187390423 Functional Loss SNV dbSNP153 33..33 33 - - - 24026 RMVar_ID_24026 Human_SNP_ID_656881701 A-to-I Human chr19 + 5913692 5913692 5913692 CCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCGCCCAGCCCACCTGGGGCATT CCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCCCAGCCCACCTGGGGCATT A G CAPS,AC104532.1 Ensembl:ENSG00000105519,Ensembl:ENSG00000267314 Protein coding,Protein coding 5'UTR,intron GSE105773;GSE126723:GSM3611827,GSM3611828,GSM3611829 Glioblastoma cells,U87MG;Bronchiolar epithelium,BEP2D cell line - 29724793,31158229 RNA-Seq:(High) rs899424603 Functional Loss SNV dbSNP153 33..33 33 - - - 24027 RMVar_ID_24027 Human_SNP_ID_656886022 A-to-I Human chr19 - 5926924 5926924 5926924 TAGTGTCGACGGGGAGGGCCCTGAAATAAACAAAAACCTCTCTAGCATGCAGAAAGCACCGGCTT TAGTGTCGACGGGGAGGGCCCTGAAATAAACAGAAACCTCTCTAGCATGCAGAAAGCACCGGCTT T C RANBP3 Ensembl:ENSG00000031823 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs936684278 Functional Loss SNV dbSNP153 33..33 33 - - - 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_27543 24028 RMVar_ID_24028 Human_SNP_ID_656909627 A-to-I Human chr19 - 6014512 6014512 6014512 AAGAAGGGCCGGGCATGGTTGCTCACGCCTGTAATCCTAGCACATTGGGAGGCCAAGGCAGGAGG AAGAAGGGCCGGGCATGGTTGCTCACGCCTGTGATCCTAGCACATTGGGAGGCCAAGGCAGGAGG T C RFX2 Ensembl:ENSG00000087903 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223083618 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_264946,RMVar_hsa_circ_330237,RMVar_hsa_circ_191781,RMVar_hsa_circ_317283,RMVar_hsa_circ_314754,RMVar_hsa_circ_191786,RMVar_hsa_circ_191783,RMVar_hsa_circ_191784,RMVar_hsa_circ_331834,RMVar_hsa_circ_372696,RMVar_hsa_circ_191787,RMVar_hsa_circ_363051 24029 RMVar_ID_24029 Human_SNP_ID_656954935 A-to-I Human chr19 - 6198895 6198895 6198895 TTTCTCAGGCTGGAGTGCAATGGCATGATCTCAGCTCACTGCGAACTCTGCCTCCTGGGTTTAAG TTTCTCAGGCTGGAGTGCAATGGCATGATCTCGGCTCACTGCGAACTCTGCCTCCTGGGTTTAAG T C RFX2 Ensembl:ENSG00000087903 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1326441536 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13530778 24030 RMVar_ID_24030 Human_SNP_ID_656962423 A-to-I Human chr19 - 6222326 6222323 6222326 CTCGCCAAAGCCCAGCGCCAAGAAGCAGAAGAAGAGCAGCTCGAAGGGGTCCCGGAGTGCTCCAG CTCGCCAAAGCCCAGCGCCAAGAAGCAGAAGA___GCAGCTCGAAGGGGTCCCGGAGTGCTCCAG CTCT C MLLT1 Ensembl:ENSG00000130382 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) 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 24031 RMVar_ID_24031 Human_SNP_ID_656965240 A-to-I Human chr19 - 6232064 6232064 6232064 GCTCGGCTAATTTTTGTATTTTTAGTGGAGACAGGGTTTCGCCACGTAGCCCAGGCTGGTCTCAA GCTCGGCTAATTTTTGTATTTTTAGTGGAGACGGGGTTTCGCCACGTAGCCCAGGCTGGTCTCAA T C MLLT1 Ensembl:ENSG00000130382 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1269502907 Functional Loss SNV dbSNP153 33..33 33 - - - 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 24032 RMVar_ID_24032 Human_SNP_ID_657002219 A-to-I Human chr19 + 6362969 6362969 6362969 AAGATTAGCCGGGCAATGTGGCGTGTGCCTGTAGTCCCAGCAACTCGGAAGGCTGAGGGAGAAGG AAGATTAGCCGGGCAATGTGGCGTGTGCCTGTGGTCCCAGCAACTCGGAAGGCTGAGGGAGAAGG A G CLPP Ensembl:ENSG00000125656 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223028675 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121228,RMVar_hsa_circ_103911,RMVar_hsa_circ_191807,RMVar_hsa_circ_191808,RMVar_hsa_circ_315727 24033 RMVar_ID_24033 Human_SNP_ID_657003002 A-to-I Human chr19 + 6365456 6365456 6365456 AGATTGCGCCACTGCACTCAAGCCTGGATGACAGAGCAAGACTCTGTCTCAAAACAACAAAGGGA AGATTGCGCCACTGCACTCAAGCCTGGATGACGGAGCAAGACTCTGTCTCAAAACAACAAAGGGA A G CLPP Ensembl:ENSG00000125656 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1347691707 Functional Loss SNV dbSNP153 33..33 33 - - - 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_191811 24034 RMVar_ID_24034 Human_SNP_ID_657003410 A-to-I Human chr19 + 6366840 6366840 6366840 TTTTGTAGAGACGTGGTTTCACCATGTTGCCCAGGCTGGTCTCAAACTCGTGAGCTCAAGTGATC TTTTGTAGAGACGTGGTTTCACCATGTTGCCCGGGCTGGTCTCAAACTCGTGAGCTCAAGTGATC A G CLPP Ensembl:ENSG00000125656 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1279273939 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121228,RMVar_hsa_circ_103911,RMVar_hsa_circ_191807,RMVar_hsa_circ_191808,RMVar_hsa_circ_85054,RMVar_hsa_circ_191811,RMVar_hsa_circ_101255,RMVar_hsa_circ_191812 24035 RMVar_ID_24035 Human_SNP_ID_657003421 A-to-I Human chr19 + 6366883 6366883 6366883 AAACTCGTGAGCTCAAGTGATCCAGCTGCCTCAGCCTCCCAAAGTTCTGGGATTACAAGTGTGAG AAACTCGTGAGCTCAAGTGATCCAGCTGCCTCGGCCTCCCAAAGTTCTGGGATTACAAGTGTGAG A G CLPP Ensembl:ENSG00000125656 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1194190666 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121228,RMVar_hsa_circ_103911,RMVar_hsa_circ_191807,RMVar_hsa_circ_191808,RMVar_hsa_circ_85054,RMVar_hsa_circ_191811,RMVar_hsa_circ_101255,RMVar_hsa_circ_191812 24036 RMVar_ID_24036 Human_SNP_ID_657003425 A-to-I Human chr19 + 6366905 6366905 6366905 CAGCTGCCTCAGCCTCCCAAAGTTCTGGGATTACAAGTGTGAGCCACCACGCCCAGCCATAATTT CAGCTGCCTCAGCCTCCCAAAGTTCTGGGATTTCAAGTGTGAGCCACCACGCCCAGCCATAATTT A T CLPP Ensembl:ENSG00000125656 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs943891568 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121228,RMVar_hsa_circ_103911,RMVar_hsa_circ_191807,RMVar_hsa_circ_191808,RMVar_hsa_circ_85054,RMVar_hsa_circ_191811,RMVar_hsa_circ_101255,RMVar_hsa_circ_191812 24037 RMVar_ID_24037 Human_SNP_ID_657003512 A-to-I Human chr19 + 6367221 6367220 6367221 ACATGGTGAAACCCCGTCTCTACCAAAAATACAAAAACTAGCCAGGTGTGTTGGCACACGCCTGT ACATGGTGAAACCCCGTCTCTACCAAAAATAC_AAAACTAGCCAGGTGTGTTGGCACACGCCTGT CA C CLPP Ensembl:ENSG00000125656 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs761114198 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_121228,RMVar_hsa_circ_103911,RMVar_hsa_circ_191807,RMVar_hsa_circ_191808,RMVar_hsa_circ_85054,RMVar_hsa_circ_191811,RMVar_hsa_circ_101255,RMVar_hsa_circ_191812 24038 RMVar_ID_24038 Human_SNP_ID_657007094 A-to-I Human chr19 - 6377363 6377363 6377363 CAGTATCGCTCTGTCGCCCAGGTTTGAGTGCAATGGCACAATCTCAGCTCACTGCAACCTCCACC CAGTATCGCTCTGTCGCCCAGGTTTGAGTGCATTGGCACAATCTCAGCTCACTGCAACCTCCACC T A PSPN Ensembl:ENSG00000125650 Protein coding 5'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs572050274 Functional Loss SNV dbSNP153 33..33 33 - - - 24039 RMVar_ID_24039 Human_SNP_ID_657007095 A-to-I Human chr19 - 6377363 6377363 6377363 CAGTATCGCTCTGTCGCCCAGGTTTGAGTGCAATGGCACAATCTCAGCTCACTGCAACCTCCACC CAGTATCGCTCTGTCGCCCAGGTTTGAGTGCAGTGGCACAATCTCAGCTCACTGCAACCTCCACC T C PSPN Ensembl:ENSG00000125650 Protein coding 5'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs572050274 Functional Loss SNV dbSNP153 33..33 33 - - - 24040 RMVar_ID_24040 Human_SNP_ID_657009466 A-to-I Human chr19 - 6384080 6384080 6384080 AACAAAAGATCTGGCTGGGCACGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGT AACAAAAGATCTGGCTGGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGT T C GTF2F1 Ensembl:ENSG00000125651 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs925071050 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37016,RMVar_hsa_circ_120161,RMVar_hsa_circ_191821 24041 RMVar_ID_24041 Human_SNP_ID_657009545 A-to-I Human chr19 - 6384392 6384392 6384392 TTGATTCTCCTCCCTCAGCCTCCTGAGTAGTCAGGACTACAGGCACATGCCACCACGCCCGGCTA TTGATTCTCCTCCCTCAGCCTCCTGAGTAGTCGGGACTACAGGCACATGCCACCACGCCCGGCTA T C GTF2F1 Ensembl:ENSG00000125651 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1264780682 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37016,RMVar_hsa_circ_120161,RMVar_hsa_circ_191821 24042 RMVar_ID_24042 Human_SNP_ID_657009702 A-to-I Human chr19 - 6384916 6384916 6384916 AGCCAGGCATGGTGGCGGGCACCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCT AGCCAGGCATGGTGGCGGGCACCTGTAATCCCGGCTACTCGGGAGGCTGAGGCAGGAGAATTGCT T C GTF2F1 Ensembl:ENSG00000125651 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1041573324 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37016,RMVar_hsa_circ_120161,RMVar_hsa_circ_191821 24043 RMVar_ID_24043 Human_SNP_ID_657009703 A-to-I Human chr19 - 6384921 6384921 6384921 AAATTAGCCAGGCATGGTGGCGGGCACCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAA AAATTAGCCAGGCATGGTGGCGGGCACCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAA T C GTF2F1 Ensembl:ENSG00000125651 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1279620863 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37016,RMVar_hsa_circ_120161,RMVar_hsa_circ_191821 24044 RMVar_ID_24044 Human_SNP_ID_657010079 A-to-I Human chr19 - 6386202 6386202 6386202 CTTTGTATTTTTTGTAGAGACAGGGTTTCACCATGTTGGCCAGGTGGTCTCAAACTCCTAACCTC CTTTGTATTTTTTGTAGAGACAGGGTTTCACCCTGTTGGCCAGGTGGTCTCAAACTCCTAACCTC T G GTF2F1 Ensembl:ENSG00000125651 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1337854921 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37016,RMVar_hsa_circ_120161,RMVar_hsa_circ_191821 24045 RMVar_ID_24045 Human_SNP_ID_657010106 A-to-I Human chr19 - 6386301 6386301 6386301 TCACTGCAACCTCCGACTCCTAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGAGAAAT TCACTGCAACCTCCGACTCCTAGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCCAAGTAGAGAAAT T C GTF2F1 Ensembl:ENSG00000125651 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs887975572 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37016,RMVar_hsa_circ_120161,RMVar_hsa_circ_191821 24046 RMVar_ID_24046 Human_SNP_ID_657019342 A-to-I Human chr19 - 6414526 6414526 6414526 CGCGCTTGCCTGTGTCCCGGGCTTGTCTGTGAAGTGGGCGTGAAGATCGTTGCCACCTTCCAACC CGCGCTTGCCTGTGTCCCGGGCTTGTCTGTGAGGTGGGCGTGAAGATCGTTGCCACCTTCCAACC T C KHSRP Ensembl:ENSG00000088247 Protein coding intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1329153469 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_528884,Human_RBP_ID_1095179,Human_RBP_ID_1192111,Human_RBP_ID_1574209,Human_RBP_ID_1893534,Human_RBP_ID_3578736,Human_RBP_ID_4574439,Human_RBP_ID_6793024,Human_RBP_ID_8197497,Human_RBP_ID_8496422,Human_RBP_ID_9353681,Human_RBP_ID_13531499,Human_RBP_ID_17271299,Human_RBP_ID_18307703,Human_RBP_ID_18741825,Human_RBP_ID_20435836,Human_RBP_ID_22813225,Human_RBP_ID_23131918,Human_RBP_ID_23181178,Human_RBP_ID_23810801,Human_RBP_ID_24485168,Human_RBP_ID_26470829,Human_RBP_ID_26997255,Human_RBP_ID_27279926 24047 RMVar_ID_24047 Human_SNP_ID_657019535 A-to-I Human chr19 - 6414963 6414963 6414963 GGTCTCCGGGAGTCCCCACGCACCGCCAGGGAAGCATTCGCTGGGTCCAGAGGTTAAACGAAGAG GGTCTCCGGGAGTCCCCACGCACCGCCAGGGATGCATTCGCTGGGTCCAGAGGTTAAACGAAGAG T A KHSRP Ensembl:ENSG00000088247 Protein coding intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1281264234 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_528896,Human_RBP_ID_1574220,Human_RBP_ID_1893544,Human_RBP_ID_6793047,Human_RBP_ID_8199372,Human_RBP_ID_17933542,Human_RBP_ID_18741840,Human_RBP_ID_22069602,Human_RBP_ID_22812848,Human_RBP_ID_23181187,Human_RBP_ID_23810807,Human_RBP_ID_27279935 24048 RMVar_ID_24048 Human_SNP_ID_657028152 A-to-I Human chr19 - 6438516 6438516 6438516 TTTTGTGGAAATAGGATTTCATCATGTTGCCCAGGCTCATCTCGAACTCGTGGGGTCAAGGAATT TTTTGTGGAAATAGGATTTCATCATGTTGCCCGGGCTCATCTCGAACTCGTGGGGTCAAGGAATT T C SLC25A23 Ensembl:ENSG00000125648 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs971242521 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1944764,Human_Splice_Rec_1944765,Human_Splice_Rec_1944788,Human_Splice_Rec_1944789 RMVar_hsa_circ_79615,RMVar_hsa_circ_87991,RMVar_hsa_circ_191829,RMVar_hsa_circ_191830 24049 RMVar_ID_24049 Human_SNP_ID_657032872 A-to-I Human chr19 - 6455994 6455994 6455994 ACGGTCTTGGCCAGGCGCAGTGGCTCACACCTAAAATCCCAGCACTTTGGGAGGCCGAAGTGGGC ACGGTCTTGGCCAGGCGCAGTGGCTCACACCTGAAATCCCAGCACTTTGGGAGGCCGAAGTGGGC T C SLC25A23 Ensembl:ENSG00000125648 Protein coding CDS GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs17849521 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1944774,Human_Splice_Rec_1944775 RMVar_hsa_circ_79615,RMVar_hsa_circ_191830,RMVar_hsa_circ_96928,RMVar_hsa_circ_191835 24050 RMVar_ID_24050 Human_SNP_ID_657046064 A-to-I Human chr19 - 6497811 6497811 6497811 CTGCAGGCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCCGCCACCTCGCCCGGCTAATTTTT CTGCAGGCTCAGCCTCCCGAGTAGCTGGGACTGCAGGCGCCCGCCACCTCGCCCGGCTAATTTTT T C TUBB4A Ensembl:ENSG00000104833 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1393747621 Functional Loss SNV dbSNP153 33..33 33 - - - 24051 RMVar_ID_24051 Human_SNP_ID_657057733 A-to-I Human chr19 + 6537166 6537166 6537166 TGGTCTTGAACTCCGAGCAACGCTCCTGCCTCAGACTCCCAAAGTGCCAGGATTACAGGTGTAAG TGGTCTTGAACTCCGAGCAACGCTCCTGCCTCGGACTCCCAAAGTGCCAGGATTACAGGTGTAAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs547876401 Functional Loss SNV dbSNP153 33..33 33 - - - 24052 RMVar_ID_24052 Human_SNP_ID_657057737 A-to-I Human chr19 + 6537182 6537182 6537182 GCAACGCTCCTGCCTCAGACTCCCAAAGTGCCAGGATTACAGGTGTAAGGCACCAGGCCCGAACT GCAACGCTCCTGCCTCAGACTCCCAAAGTGCCGGGATTACAGGTGTAAGGCACCAGGCCCGAACT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1439881880 Functional Loss SNV dbSNP153 33..33 33 - - - 24053 RMVar_ID_24053 Human_SNP_ID_657069085 A-to-I Human chr19 - 6579486 6579486 6579486 TTGATCAGAGCTGGGCGGGGTGGCTCACACCTATAATCCCAGCACTTTGGGAGGCCAAGGTGGGC TTGATCAGAGCTGGGCGGGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGC T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs143120665 Functional Loss SNV dbSNP153 33..33 33 - - - 24054 RMVar_ID_24054 Human_SNP_ID_657069246 A-to-I Human chr19 - 6580115 6580109 6580115 CCTTGGCCTCCCAAAGAGCTAGGATTACAGGCATGAGCTGCTGTGCCCAGCCTCATCTTTTGAAA CCTTGGCCTCCCAAAGAGCTAGGATTACAGGC______TGCTGTGCCCAGCCTCATCTTTTGAAA AGCTCAT A - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1266605577 Functional Loss DEL dbSNP153 33..38 33 - - - 24055 RMVar_ID_24055 Human_SNP_ID_657070327 A-to-I Human chr19 - 6583622 6583622 6583622 CTCAGGAGGTGGAGATTGCAGTGAGCTGAGATAGTGCCACTGCACTCCAGCCTGGGTGGCAGAGT CTCAGGAGGTGGAGATTGCAGTGAGCTGAGATGGTGCCACTGCACTCCAGCCTGGGTGGCAGAGT T C CD70 Ensembl:ENSG00000125726 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1421567261 Functional Loss SNV dbSNP153 33..33 33 - - - 24056 RMVar_ID_24056 Human_SNP_ID_657070348 A-to-I Human chr19 - 6583697 6583697 6583697 AAAATTAGCTGGGTGTGGTGATGGGCACCTCTAATCCATGCTACTAGGGAGGCTGAGACAGGAGA AAAATTAGCTGGGTGTGGTGATGGGCACCTCTGATCCATGCTACTAGGGAGGCTGAGACAGGAGA T C CD70 Ensembl:ENSG00000125726 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs529569103 Functional Loss SNV dbSNP153 33..33 33 - - - 24057 RMVar_ID_24057 Human_SNP_ID_657070356 A-to-I Human chr19 - 6583726 6583726 6583726 GGTGAAACCTCATCTCTACTAAACATTTAAAAATTAGCTGGGTGTGGTGATGGGCACCTCTAATC GGTGAAACCTCATCTCTACTAAACATTTAAAAGTTAGCTGGGTGTGGTGATGGGCACCTCTAATC T C CD70 Ensembl:ENSG00000125726 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1187138208 Functional Loss SNV dbSNP153 33..33 33 - - - 24058 RMVar_ID_24058 Human_SNP_ID_657070408 A-to-I Human chr19 - 6583855 6583855 6583855 CCCGGAGGTGGAGGTTGCAGTGAGCCAAGATCATGTCATTGCACTCCAGCCTGGGTGACAAGAGC CCCGGAGGTGGAGGTTGCAGTGAGCCAAGATCTTGTCATTGCACTCCAGCCTGGGTGACAAGAGC T A CD70 Ensembl:ENSG00000125726 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1279158202 Functional Loss SNV dbSNP153 33..33 33 - - - 24059 RMVar_ID_24059 Human_SNP_ID_657070581 A-to-I Human chr19 - 6584454 6584454 6584454 TTGTCCAGGCTGGAGTGCAGTGGCATAATCTCAGCTCACTGCAACCTCCACCCTCCCAGGTTCAA TTGTCCAGGCTGGAGTGCAGTGGCATAATCTCGGCTCACTGCAACCTCCACCCTCCCAGGTTCAA T C CD70 Ensembl:ENSG00000125726 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs764840690 Functional Loss SNV dbSNP153 33..33 33 - - - 24060 RMVar_ID_24060 Human_SNP_ID_657070582 A-to-I Human chr19 - 6584454 6584454 6584454 TTGTCCAGGCTGGAGTGCAGTGGCATAATCTCAGCTCACTGCAACCTCCACCCTCCCAGGTTCAA TTGTCCAGGCTGGAGTGCAGTGGCATAATCTCCGCTCACTGCAACCTCCACCCTCCCAGGTTCAA T G CD70 Ensembl:ENSG00000125726 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs764840690 Functional Loss SNV dbSNP153 33..33 33 - - - 24061 RMVar_ID_24061 Human_SNP_ID_657070583 A-to-I Human chr19 - 6584459 6584459 6584459 CCCTGTTGTCCAGGCTGGAGTGCAGTGGCATAATCTCAGCTCACTGCAACCTCCACCCTCCCAGG CCCTGTTGTCCAGGCTGGAGTGCAGTGGCATAGTCTCAGCTCACTGCAACCTCCACCCTCCCAGG T C CD70 Ensembl:ENSG00000125726 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs528708758 Functional Loss SNV dbSNP153 33..33 33 - - - 24062 RMVar_ID_24062 Human_SNP_ID_657070629 A-to-I Human chr19 - 6584615 6584615 6584615 GAAATGCCGATCTTCCCGCCTCGGTCTCCCCAAGTGCTGGGATTACAGGCATGAGCCACTGCCTG GAAATGCCGATCTTCCCGCCTCGGTCTCCCCAGGTGCTGGGATTACAGGCATGAGCCACTGCCTG T C CD70 Ensembl:ENSG00000125726 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1349174256 Functional Loss SNV dbSNP153 33..33 33 - - - 24063 RMVar_ID_24063 Human_SNP_ID_657070888 A-to-I Human chr19 - 6585484 6585484 6585484 ATACAAAAATTAACCAGATGTAGTGGTGTGCTAGTCCAAGCTACTCCAAAGGCTGAAGTGGGAGA ATACAAAAATTAACCAGATGTAGTGGTGTGCTTGTCCAAGCTACTCCAAAGGCTGAAGTGGGAGA T A CD70 Ensembl:ENSG00000125726 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1160764910 Functional Loss SNV dbSNP153 33..33 33 - - - 24064 RMVar_ID_24064 Human_SNP_ID_657070979 A-to-I Human chr19 - 6585812 6585812 6585812 AAATCAGCTGGGCTTCGTGGCGTGCATCTGTAATCCCAGCTACTCGGCCGACTGAGGCAGGAGAA AAATCAGCTGGGCTTCGTGGCGTGCATCTGTAGTCCCAGCTACTCGGCCGACTGAGGCAGGAGAA T C CD70 Ensembl:ENSG00000125726 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs979431151 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2572127 24065 RMVar_ID_24065 Human_SNP_ID_657071708 A-to-I Human chr19 - 6587778 6587778 6587778 TTGAGCCCCAGAGGCTGAGGCTGCAGTGAGCTATGATTGCACCACTGCACTCCAGCCTGGGTGAC TTGAGCCCCAGAGGCTGAGGCTGCAGTGAGCTGTGATTGCACCACTGCACTCCAGCCTGGGTGAC T C CD70 Ensembl:ENSG00000125726 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1278725662 Functional Loss SNV dbSNP153 33..33 33 - - - 24066 RMVar_ID_24066 Human_SNP_ID_657071729 A-to-I Human chr19 - 6587874 6587874 6587874 AAGACCACCATCTCTAGAACAAAATTTTGAAAATTAGCTGGTCATGGTGGCGCATGCCACCTCCC AAGACCACCATCTCTAGAACAAAATTTTGAAACTTAGCTGGTCATGGTGGCGCATGCCACCTCCC T G CD70 Ensembl:ENSG00000125726 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs944682371 Functional Loss SNV dbSNP153 33..33 33 - - - 24067 RMVar_ID_24067 Human_SNP_ID_657113960 A-to-I Human chr19 - 6732111 6732108 6732112 GTGGCCTACATCATCATCGAGTCCCGCGAGGAAGGCGCCAGCGACTACGTGCTGTGGAAGGAGAT GTGGCCTACATCATCATCGAGTCCCGCGAGG____CGCCAGCGACTACGTGCTGTGGAAGGAGAT GCCTT G GPR108 Ensembl:ENSG00000125734 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1568236917 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_9380237,Human_RBP_ID_18994164,Human_RBP_ID_26337205 Human_Splice_Rec_1945470,Human_Splice_Rec_1945471,Human_Splice_Rec_1945481,Human_Splice_Rec_1945489,Human_Splice_Rec_1945499,Human_Splice_Rec_1945510,Human_Splice_Rec_1945511,Human_Splice_Rec_1945542,Human_Splice_Rec_1945543,Human_Splice_Rec_1945576,Human_Splice_Rec_1945577,Human_Splice_Rec_1945610,Human_Splice_Rec_1945611,Human_Splice_Rec_1945626,Human_Splice_Rec_1945627,Human_Splice_Rec_1945636 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 24068 RMVar_ID_24068 Human_SNP_ID_657119164 A-to-I Human chr19 + 6746816 6746816 6746816 CTAGGACCACAGGCATGCACCAGCTAATTTTTATATTTTTAGTAGAGGCGGGGTTTCCCCATATT CTAGGACCACAGGCATGCACCAGCTAATTTTTGTATTTTTAGTAGAGGCGGGGTTTCCCCATATT A G TRIP10 Ensembl:ENSG00000125733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1183845173 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48554,RMVar_hsa_circ_112314,RMVar_hsa_circ_119444,RMVar_hsa_circ_191911,RMVar_hsa_circ_191913 24069 RMVar_ID_24069 Human_SNP_ID_657119231 A-to-I Human chr19 + 6747104 6747104 6747104 CCAGCATTTTGGGAGGTTGAGGCAGGAGGATCATCTGAGCCTAGGAGTTTGAGACCTGCCTGGGC CCAGCATTTTGGGAGGTTGAGGCAGGAGGATCGTCTGAGCCTAGGAGTTTGAGACCTGCCTGGGC A G TRIP10 Ensembl:ENSG00000125733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1303335235 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48554,RMVar_hsa_circ_112314,RMVar_hsa_circ_119444,RMVar_hsa_circ_191911,RMVar_hsa_circ_191913 24070 RMVar_ID_24070 Human_SNP_ID_657119599 A-to-I Human chr19 - 6748693 6748693 6748693 TGCCTCCCGGGATCAAGTGATTCTCGTGCCTCAGCCTCTGGAGTAGCTGGGACTACAGGCACACG TGCCTCCCGGGATCAAGTGATTCTCGTGCCTCGGCCTCTGGAGTAGCTGGGACTACAGGCACACG T C AC008760.1 Ensembl:ENSG00000269680 lincRNA exon GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1190584608 Functional Loss SNV dbSNP153 33..33 33 - - - 24071 RMVar_ID_24071 Human_SNP_ID_657130372 A-to-I Human chr19 + 6785793 6785793 6785793 ATGATTCTCCTGCCTCAGCCTTCCGAGTAGCCAGGATTATAGGGACGCACCACCACACCCAGCTA ATGATTCTCCTGCCTCAGCCTTCCGAGTAGCCGGGATTATAGGGACGCACCACCACACCCAGCTA A G VAV1 Ensembl:ENSG00000141968 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs942539286 Functional Loss SNV dbSNP153 33..33 33 - - - 24072 RMVar_ID_24072 Human_SNP_ID_657142504 A-to-I Human chr19 + 6830543 6830543 6830543 CTCACTGCAACCTCTGGCTCCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGG CTCACTGCAACCTCTGGCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGG A G VAV1 Ensembl:ENSG00000141968 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1323004584 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98186,RMVar_hsa_circ_191922 24073 RMVar_ID_24073 Human_SNP_ID_657142511 A-to-I Human chr19 + 6830569 6830569 6830569 TCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACGGGCACCCACCACCATGCCCA TCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTCGCTGGGATTACGGGCACCCACCACCATGCCCA A C VAV1 Ensembl:ENSG00000141968 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1031858252 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98186,RMVar_hsa_circ_191922 24074 RMVar_ID_24074 Human_SNP_ID_657142543 A-to-I Human chr19 + 6830714 6830714 6830714 TGCCCATCTTGGCCTCCCAAAGTGCTGAGATTACAAGCGTGAGCCACTGTGCCCAGCTTATTTTA TGCCCATCTTGGCCTCCCAAAGTGCTGAGATTGCAAGCGTGAGCCACTGTGCCCAGCTTATTTTA A G VAV1 Ensembl:ENSG00000141968 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1396119941 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98186,RMVar_hsa_circ_191922 24075 RMVar_ID_24075 Human_SNP_ID_657142600 A-to-I Human chr19 + 6830971 6830971 6830971 AAATTTAGCTGGGCTTGGTGGCACATGCCTGTAGCCCTAGCTACATGGGAGGCTGAGGTGGGAGG AAATTTAGCTGGGCTTGGTGGCACATGCCTGTTGCCCTAGCTACATGGGAGGCTGAGGTGGGAGG A T VAV1 Ensembl:ENSG00000141968 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1332654838 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98186,RMVar_hsa_circ_191922 24076 RMVar_ID_24076 Human_SNP_ID_657147316 A-to-I Human chr19 + 6847097 6847097 6847097 CATCAAGCCCAGCTAATTTTTGCATTTTTAGTAGAGACGAGGTTTCACCATGTTGCCCAGGCTGG CATCAAGCCCAGCTAATTTTTGCATTTTTAGTGGAGACGAGGTTTCACCATGTTGCCCAGGCTGG A G VAV1 Ensembl:ENSG00000141968 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1175157615 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98186,RMVar_hsa_circ_191922,RMVar_hsa_circ_66140,RMVar_hsa_circ_191925,RMVar_hsa_circ_369270 24077 RMVar_ID_24077 Human_SNP_ID_657213910 A-to-I Human chr19 + 7084382 7084378 7084382 CCCTCATTTTTTTTTTTTTAAGACAATGTCTCACTCTGTCACCCAGTCTGGAGCGCAGTGGTGTG CCCTCATTTTTTTTTTTTTAAGACAATGT____CTCTGTCACCCAGTCTGGAGCGCAGTGGTGTG TCTCA T ZNF557 Ensembl:ENSG00000130544 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1189588846 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_13532314,Human_RBP_ID_17933662 RMVar_hsa_circ_119477,RMVar_hsa_circ_191931 24078 RMVar_ID_24078 Human_SNP_ID_657213925 A-to-I Human chr19 + 7084437 7084437 7084437 CAGTGGTGTGATCACAGCTCACTGCAGCCTCTACTTCCTGGGATCAAGTAATTCTCCTGCCCCAG CAGTGGTGTGATCACAGCTCACTGCAGCCTCTCCTTCCTGGGATCAAGTAATTCTCCTGCCCCAG A C ZNF557 Ensembl:ENSG00000130544 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs767740056 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119477,RMVar_hsa_circ_191931 24079 RMVar_ID_24079 Human_SNP_ID_657213928 A-to-I Human chr19 + 7084447 7084447 7084447 ATCACAGCTCACTGCAGCCTCTACTTCCTGGGATCAAGTAATTCTCCTGCCCCAGCCTCCAATGT ATCACAGCTCACTGCAGCCTCTACTTCCTGGGCTCAAGTAATTCTCCTGCCCCAGCCTCCAATGT A C ZNF557 Ensembl:ENSG00000130544 Protein coding 3'UTR GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs904287378 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119477,RMVar_hsa_circ_191931 24080 RMVar_ID_24080 Human_SNP_ID_657213938 A-to-I Human chr19 + 7084490 7084490 7084490 CTCCTGCCCCAGCCTCCAATGTAGCTGGGACTACAGGTGCATGACACCATGTCTGGCTAATTTGT CTCCTGCCCCAGCCTCCAATGTAGCTGGGACTGCAGGTGCATGACACCATGTCTGGCTAATTTGT A G ZNF557 Ensembl:ENSG00000130544 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs529078387 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119477,RMVar_hsa_circ_191931 24081 RMVar_ID_24081 Human_SNP_ID_657214311 A-to-I Human chr19 + 7085972 7085972 7085972 TAGACATTTGCCAGGTGTGGTGGCTCACACCTATAAACCTAGCATTTTGGGAGGCTGAGGCGGGC TAGACATTTGCCAGGTGTGGTGGCTCACACCTGTAAACCTAGCATTTTGGGAGGCTGAGGCGGGC A G ZNF557 Ensembl:ENSG00000130544 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1169832123 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119477,RMVar_hsa_circ_191931 24082 RMVar_ID_24082 Human_SNP_ID_657214312 A-to-I Human chr19 + 7085974 7085974 7085974 GACATTTGCCAGGTGTGGTGGCTCACACCTATAAACCTAGCATTTTGGGAGGCTGAGGCGGGCAG GACATTTGCCAGGTGTGGTGGCTCACACCTATGAACCTAGCATTTTGGGAGGCTGAGGCGGGCAG A G ZNF557 Ensembl:ENSG00000130544 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs539335050 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13532339 RMVar_hsa_circ_119477,RMVar_hsa_circ_191931 24083 RMVar_ID_24083 Human_SNP_ID_657214475 A-to-I Human chr19 + 7086410 7086410 7086410 TTGAGACGGAGTCTTGCTCTGTTGTCCAGGCTAGAATGCAGTGGCGCGATTGTGGCTCACTGCAA TTGAGACGGAGTCTTGCTCTGTTGTCCAGGCTGGAATGCAGTGGCGCGATTGTGGCTCACTGCAA A G ZNF557 Ensembl:ENSG00000130544 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1194176986 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119477,RMVar_hsa_circ_191931 24084 RMVar_ID_24084 Human_SNP_ID_657214481 A-to-I Human chr19 + 7086441 7086441 7086441 TAGAATGCAGTGGCGCGATTGTGGCTCACTGCAAGCTCTGCCTCCCAGATTCACGCCATCCTCCT TAGAATGCAGTGGCGCGATTGTGGCTCACTGCGAGCTCTGCCTCCCAGATTCACGCCATCCTCCT A G ZNF557 Ensembl:ENSG00000130544 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs948742801 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119477,RMVar_hsa_circ_191931 24085 RMVar_ID_24085 Human_SNP_ID_657214498 A-to-I Human chr19 + 7086511 7086510 7086512 AGCCTCCCGAGTAGCTGGGACTACAGGTGCCCATCACCATGCCCGGCTAATTTTTCATATTTTTA AGCCTCCCGAGTAGCTGGGACTACAGGTGCCC__CACCATGCCCGGCTAATTTTTCATATTTTTA CAT C ZNF557 Ensembl:ENSG00000130544 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1447230873 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_119477,RMVar_hsa_circ_191931 24086 RMVar_ID_24086 Human_SNP_ID_657214506 A-to-I Human chr19 + 7086543 7086543 7086543 ATCACCATGCCCGGCTAATTTTTCATATTTTTAGTAGAAATGGGGTTTCACTGTGTTAGCCAGTA ATCACCATGCCCGGCTAATTTTTCATATTTTTGGTAGAAATGGGGTTTCACTGTGTTAGCCAGTA A G ZNF557 Ensembl:ENSG00000130544 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1339261243 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119477,RMVar_hsa_circ_191931 24087 RMVar_ID_24087 Human_SNP_ID_657214530 A-to-I Human chr19 + 7086621 7086619 7086621 CTGACCTCGTGATCCACCTGCCTCGGCCTCCCAAAGCACTGGGATTACAGGCGTGAGCCACCATG CTGACCTCGTGATCCACCTGCCTCGGCCTCC__AAGCACTGGGATTACAGGCGTGAGCCACCATG CCA C ZNF557 Ensembl:ENSG00000130544 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1271069586 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_119477,RMVar_hsa_circ_191931 24088 RMVar_ID_24088 Human_SNP_ID_657214819 A-to-I Human chr19 + 7087345 7087345 7087345 GGCGGATCACCTGAGGTGGGGAGTTCGAGACCAGCCTGATCAACATGGAGAAAACCTGTCTCTCC GGCGGATCACCTGAGGTGGGGAGTTCGAGACCGGCCTGATCAACATGGAGAAAACCTGTCTCTCC A G ZNF557 Ensembl:ENSG00000130544 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1003326651 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13532355 RMVar_hsa_circ_119477,RMVar_hsa_circ_191931 24089 RMVar_ID_24089 Human_SNP_ID_657223302 A-to-I Human chr19 - 7118403 7118403 7118403 TGAGGCAGGAGAATTGCTTGAATCGGGGAGGCAGAGGTTGCAGTGAGCAGAGACTGCACCATTGC TGAGGCAGGAGAATTGCTTGAATCGGGGAGGCGGAGGTTGCAGTGAGCAGAGACTGCACCATTGC T C INSR Ensembl:ENSG00000171105 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1435422787 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_191933,RMVar_hsa_circ_123622 24090 RMVar_ID_24090 Human_SNP_ID_657235661 A-to-I Human chr19 - 7160494 7160494 7160494 CAGCCTCCTGAGTAGCTGGACTACACAGGACTACAGGCCTGAGACACTATACCTGGCTAATTATT CAGCCTCCTGAGTAGCTGGACTACACAGGACTGCAGGCCTGAGACACTATACCTGGCTAATTATT T C INSR Ensembl:ENSG00000171105 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1033685955 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2153,RMVar_hsa_circ_191933,RMVar_hsa_circ_123622,RMVar_hsa_circ_374962,RMVar_hsa_circ_191938,RMVar_hsa_circ_79987,RMVar_hsa_circ_374746,RMVar_hsa_circ_191942,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_191948,RMVar_hsa_circ_191949,RMVar_hsa_circ_315301,RMVar_hsa_circ_353912,RMVar_hsa_circ_7350,RMVar_hsa_circ_191952,RMVar_hsa_circ_302911,RMVar_hsa_circ_191950,RMVar_hsa_circ_191951,RMVar_hsa_circ_305276,RMVar_hsa_circ_329804,RMVar_hsa_circ_3125,RMVar_hsa_circ_20827,RMVar_hsa_circ_191953 24091 RMVar_ID_24091 Human_SNP_ID_657241052 A-to-I Human chr19 - 7181662 7181662 7181662 GGGAGGCTGAGGCATGAGAATTGCTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCTGAGATCACG GGGAGGCTGAGGCATGAGAATTGCTTGAACCCGGGAGGCAGAGGTTGCAGTGAGCTGAGATCACG T C INSR Ensembl:ENSG00000171105 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1454436611 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_374746,RMVar_hsa_circ_191942,RMVar_hsa_circ_106893,RMVar_hsa_circ_191949,RMVar_hsa_circ_353912,RMVar_hsa_circ_191954,RMVar_hsa_circ_191951,RMVar_hsa_circ_3125,RMVar_hsa_circ_20827,RMVar_hsa_circ_319004,RMVar_hsa_circ_292925,RMVar_hsa_circ_60628,RMVar_hsa_circ_356491 24092 RMVar_ID_24092 Human_SNP_ID_657253736 A-to-I Human chr19 - 7226641 7226641 7226641 TTACTGTAGCCTTGACCTCTTGGGCTCAAGCAATCCTCCCACTTCAGCTTCCCGAGTAGCTGGGA TTACTGTAGCCTTGACCTCTTGGGCTCAAGCAGTCCTCCCACTTCAGCTTCCCGAGTAGCTGGGA T C INSR Ensembl:ENSG00000171105 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1001176569 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 24093 RMVar_ID_24093 Human_SNP_ID_657257787 A-to-I Human chr19 - 7242065 7242065 7242065 CACTGCAATTTCTGCCTCCTGAGTTCAAAGCAATTCTCCTGCCTCAGCCTCCTAAGCAGCTGGGA CACTGCAATTTCTGCCTCCTGAGTTCAAAGCAGTTCTCCTGCCTCAGCCTCCTAAGCAGCTGGGA T C INSR Ensembl:ENSG00000171105 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1052698607 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 24094 RMVar_ID_24094 Human_SNP_ID_657261369 A-to-I Human chr19 - 7254443 7254441 7254443 CTCACTGCAGCCTCAGCCTTTTGGGCTCAAGCAATCCTCCAGCCTCAGCCTGGCCAGTAGCTGGA CTCACTGCAGCCTCAGCCTTTTGGGCTCAAGC__TCCTCCAGCCTCAGCCTGGCCAGTAGCTGGA ATT A INSR Ensembl:ENSG00000171105 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1441699723 Functional Loss DEL dbSNP153 33..34 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 24095 RMVar_ID_24095 Human_SNP_ID_657299016 A-to-I Human chr19 + 7397837 7397837 7397837 GCGATCCTCCCACCTCGGCCTCCCAAAGTGCTAGGATTACAGGCGTGAGCTGCCACAGCCTGTGG GCGATCCTCCCACCTCGGCCTCCCAAAGTGCTTGGATTACAGGCGTGAGCTGCCACAGCCTGTGG A T AC008878.3,ARHGEF18 Ensembl:ENSG00000268861,Ensembl:ENSG00000104880 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs899007184 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23811154 RMVar_hsa_circ_191972,RMVar_hsa_circ_86296 24096 RMVar_ID_24096 Human_SNP_ID_657299928 A-to-I Human chr19 + 7401433 7401433 7401433 TCAGCCTCCCAAATAGCTGGAACCACAGGCACACACCATCACGCCTGGCTAATTTTTTTTTATTT TCAGCCTCCCAAATAGCTGGAACCACAGGCACGCACCATCACGCCTGGCTAATTTTTTTTTATTT A G AC008878.3,ARHGEF18 Ensembl:ENSG00000268861,Ensembl:ENSG00000104880 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1451344812 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_191972,RMVar_hsa_circ_86296 24097 RMVar_ID_24097 Human_SNP_ID_657300054 A-to-I Human chr19 + 7402079 7402079 7402079 TGCCACAGGCTGGGGGTAGTGGAGTGGGGAGTAATGGCCAAGGTAATGGGGTTTCTTTTTGAGGT TGCCACAGGCTGGGGGTAGTGGAGTGGGGAGTGATGGCCAAGGTAATGGGGTTTCTTTTTGAGGT A G AC008878.3,ARHGEF18 Ensembl:ENSG00000268861,Ensembl:ENSG00000104880 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2432103 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2305 RMVar_hsa_circ_191972,RMVar_hsa_circ_86296 24098 RMVar_ID_24098 Human_SNP_ID_657300067 A-to-I Human chr19 + 7402149 7402149 7402149 AGGCATTCTAAAATTGACTGTAGGCTGGGCGCAGTGGCTCATGCCTGTAATCCCAGCACTTTGGG AGGCATTCTAAAATTGACTGTAGGCTGGGCGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGG A G AC008878.3,ARHGEF18 Ensembl:ENSG00000268861,Ensembl:ENSG00000104880 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs145071480 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_191972,RMVar_hsa_circ_86296 24099 RMVar_ID_24099 Human_SNP_ID_657300123 A-to-I Human chr19 + 7402325 7402325 7402325 CCTGTAGACCCAGCTCCTCCGGAGGCTGAGGCATGAGAATTGCCTGAACCCCAGAGACGGAGGTT CCTGTAGACCCAGCTCCTCCGGAGGCTGAGGCGTGAGAATTGCCTGAACCCCAGAGACGGAGGTT A G AC008878.3,ARHGEF18 Ensembl:ENSG00000268861,Ensembl:ENSG00000104880 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs911278704 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_191972,RMVar_hsa_circ_86296 24100 RMVar_ID_24100 Human_SNP_ID_657300344 A-to-I Human chr19 + 7403339 7403339 7403339 TGTCATCACCCACAAGAAAAGCTCACACCCATAGCTTTCACTGCCCATTCCCCCATCCTCCCAGC TGTCATCACCCACAAGAAAAGCTCACACCCATGGCTTTCACTGCCCATTCCCCCATCCTCCCAGC A G AC008878.3,ARHGEF18 Ensembl:ENSG00000268861,Ensembl:ENSG00000104880 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1015891051 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_191972,RMVar_hsa_circ_86296 24101 RMVar_ID_24101 Human_SNP_ID_657301920 A-to-I Human chr19 + 7408926 7408926 7408926 AACTTACACACGCGTGGTGACTACAGGTAGGTAGTGTGCACCTATAGTCCCAGCTACTTGGGAGG AACTTACACACGCGTGGTGACTACAGGTAGGTGGTGTGCACCTATAGTCCCAGCTACTTGGGAGG A G AC008878.3,ARHGEF18 Ensembl:ENSG00000268861,Ensembl:ENSG00000104880 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs866716405 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_191972,RMVar_hsa_circ_86296 24102 RMVar_ID_24102 Human_SNP_ID_657301923 A-to-I Human chr19 + 7408937 7408937 7408937 GCGTGGTGACTACAGGTAGGTAGTGTGCACCTATAGTCCCAGCTACTTGGGAGGCTGAGGCAGGA GCGTGGTGACTACAGGTAGGTAGTGTGCACCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGA A G AC008878.3,ARHGEF18 Ensembl:ENSG00000268861,Ensembl:ENSG00000104880 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1461882605 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_191972,RMVar_hsa_circ_86296 24103 RMVar_ID_24103 Human_SNP_ID_657305226 A-to-I Human chr19 + 7420286 7420286 7420286 GGCCAGCTGAGCAATTATTATTATTTTGAGACAGGATCTTGCTCTGTTGCCCTGGCTGGAGTGCA GGCCAGCTGAGCAATTATTATTATTTTGAGACGGGATCTTGCTCTGTTGCCCTGGCTGGAGTGCA A G AC008878.3,ARHGEF18 Ensembl:ENSG00000268861,Ensembl:ENSG00000104880 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025825130 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_191972,RMVar_hsa_circ_86296 24104 RMVar_ID_24104 Human_SNP_ID_657305916 A-to-I Human chr19 + 7422939 7422939 7422939 TGGGGTTTCACCATGTTGGCCAGGCTGATCTCAAACTCCTGATCTCAAGTAATCCGCCCATCTTG TGGGGTTTCACCATGTTGGCCAGGCTGATCTCCAACTCCTGATCTCAAGTAATCCGCCCATCTTG A C AC008878.3,ARHGEF18 Ensembl:ENSG00000268861,Ensembl:ENSG00000104880 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1234147252 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_191972,RMVar_hsa_circ_86296 24105 RMVar_ID_24105 Human_SNP_ID_657307814 A-to-I Human chr19 + 7430463 7430463 7430463 GACCTTAAGTGATCCTCCCGCCTCAGCCCTGCAAAGTGCTGGAATTACAGGCATGAGCCACTGTA GACCTTAAGTGATCCTCCCGCCTCAGCCCTGCGAAGTGCTGGAATTACAGGCATGAGCCACTGTA A G AC008878.3,ARHGEF18 Ensembl:ENSG00000268861,Ensembl:ENSG00000104880 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1213777098 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_191972,RMVar_hsa_circ_86296 24106 RMVar_ID_24106 Human_SNP_ID_657307859 A-to-I Human chr19 + 7430658 7430658 7430658 GACCCTATCTCTATAAAAATATCTAAAAAATTAGCTGGGCATGGTGGTATGCGCCTATAGTCCCA GACCCTATCTCTATAAAAATATCTAAAAAATTCGCTGGGCATGGTGGTATGCGCCTATAGTCCCA A C AC008878.3,ARHGEF18 Ensembl:ENSG00000268861,Ensembl:ENSG00000104880 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037101430 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_191972,RMVar_hsa_circ_86296 24107 RMVar_ID_24107 Human_SNP_ID_657307863 A-to-I Human chr19 + 7430666 7430666 7430666 CTCTATAAAAATATCTAAAAAATTAGCTGGGCATGGTGGTATGCGCCTATAGTCCCAGCCACTTG CTCTATAAAAATATCTAAAAAATTAGCTGGGCGTGGTGGTATGCGCCTATAGTCCCAGCCACTTG A G AC008878.3,ARHGEF18 Ensembl:ENSG00000268861,Ensembl:ENSG00000104880 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs531871635 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_191972,RMVar_hsa_circ_86296 24108 RMVar_ID_24108 Human_SNP_ID_657308377 A-to-I Human chr19 + 7432499 7432499 7432499 TCTTTCTTTTTGTTTTTGTTTTGTTCAGAGACAGGGTCTCACTACGTCGCCCAGGCTGGAATACA TCTTTCTTTTTGTTTTTGTTTTGTTCAGAGACGGGGTCTCACTACGTCGCCCAGGCTGGAATACA A G AC008878.3,ARHGEF18 Ensembl:ENSG00000268861,Ensembl:ENSG00000104880 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1293665215 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_191972,RMVar_hsa_circ_86296 24109 RMVar_ID_24109 Human_SNP_ID_657310972 A-to-I Human chr19 + 7441651 7441651 7441651 TTCTAAAACAATTGTTTTTATTGTTTGCACTCAGACCAATCACAGGAGAGATGGATGAAGCCGAT TTCTAAAACAATTGTTTTTATTGTTTGCACTCCGACCAATCACAGGAGAGATGGATGAAGCCGAT A C AC008878.3,ARHGEF18 Ensembl:ENSG00000268861,Ensembl:ENSG00000104880 Protein coding,Protein coding intron,intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1488247022 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122747,RMVar_hsa_circ_191972,RMVar_hsa_circ_86296,RMVar_hsa_circ_364455,RMVar_hsa_circ_372000,RMVar_hsa_circ_342012,RMVar_hsa_circ_70597,RMVar_hsa_circ_191974,RMVar_hsa_circ_191975,RMVar_hsa_circ_310795,RMVar_hsa_circ_358740 24110 RMVar_ID_24110 Human_SNP_ID_657313539 A-to-I Human chr19 + 7450500 7450466 7450501 TTGCTTTCCGTTTCCGTTTCCGAGATGTTAATACGGGATCTTGCTGTCCATTTCCGAGATGTTAA __________________________________GGGATCTTGCTGTCCATTTCCGAGATGTTAA TCTTGCTTTCCGTTTCCGTTTCCGAGATGTTAATAC T AC008878.3,ARHGEF18 Ensembl:ENSG00000268861,Ensembl:ENSG00000104880 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1353766816 Functional Loss DEL dbSNP153 1..34 33 - - - Human_RBP_ID_825359,Human_RBP_ID_17131599,Human_RBP_ID_18492383,Human_RBP_ID_23231985 RMVar_hsa_circ_191972,RMVar_hsa_circ_86296,RMVar_hsa_circ_372000,RMVar_hsa_circ_191978,RMVar_hsa_circ_191975,RMVar_hsa_circ_118827,RMVar_hsa_circ_191979,RMVar_hsa_circ_75526,RMVar_hsa_circ_356153 24111 RMVar_ID_24111 Human_SNP_ID_657313554 A-to-I Human chr19 + 7450500 7450500 7450500 TTGCTTTCCGTTTCCGTTTCCGAGATGTTAATACGGGATCTTGCTGTCCATTTCCGAGATGTTAA TTGCTTTCCGTTTCCGTTTCCGAGATGTTAATGCGGGATCTTGCTGTCCATTTCCGAGATGTTAA A G AC008878.3,ARHGEF18 Ensembl:ENSG00000268861,Ensembl:ENSG00000104880 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1008120418 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_825359,Human_RBP_ID_17131599,Human_RBP_ID_18492383,Human_RBP_ID_23231985 RMVar_hsa_circ_191972,RMVar_hsa_circ_86296,RMVar_hsa_circ_372000,RMVar_hsa_circ_191978,RMVar_hsa_circ_191975,RMVar_hsa_circ_118827,RMVar_hsa_circ_191979,RMVar_hsa_circ_75526,RMVar_hsa_circ_356153 24112 RMVar_ID_24112 Human_SNP_ID_657314348 A-to-I Human chr19 + 7451922 7451922 7451922 TTTGATATTTGTAGTAGAGATGGGGATTCACCATGTTGATCAGGCTGGTCTTAAACTCCTGGCCT TTTGATATTTGTAGTAGAGATGGGGATTCACCGTGTTGATCAGGCTGGTCTTAAACTCCTGGCCT A G AC008878.3,ARHGEF18 Ensembl:ENSG00000268861,Ensembl:ENSG00000104880 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1212396553 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73018,RMVar_hsa_circ_191972,RMVar_hsa_circ_86296,RMVar_hsa_circ_191978,RMVar_hsa_circ_118827,RMVar_hsa_circ_191979,RMVar_hsa_circ_75526,RMVar_hsa_circ_340347 24113 RMVar_ID_24113 Human_SNP_ID_657314643 A-to-I Human chr19 + 7453088 7453088 7453088 GGGCATGGTGGCGGGTGCCTGTAATCCCAGCTACTTGGGAGACTGAGGCAGGAGAATCGCTTGAA GGGCATGGTGGCGGGTGCCTGTAATCCCAGCTGCTTGGGAGACTGAGGCAGGAGAATCGCTTGAA A G AC008878.3,ARHGEF18 Ensembl:ENSG00000268861,Ensembl:ENSG00000104880 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1018094893 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73018,RMVar_hsa_circ_191972,RMVar_hsa_circ_86296,RMVar_hsa_circ_191978,RMVar_hsa_circ_118827,RMVar_hsa_circ_191979,RMVar_hsa_circ_75526,RMVar_hsa_circ_340347 24114 RMVar_ID_24114 Human_SNP_ID_657317015 A-to-I Human chr19 + 7461727 7461727 7461727 ACAGGATCTTGCTTTGTTGGCCAGGCTGGAGTACAGTACTGCAGTCATAGCTCACTGCAGCCTTG ACAGGATCTTGCTTTGTTGGCCAGGCTGGAGTGCAGTACTGCAGTCATAGCTCACTGCAGCCTTG A G AC008878.3,ARHGEF18 Ensembl:ENSG00000268861,Ensembl:ENSG00000104880 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs990387326 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_191972,RMVar_hsa_circ_86296,RMVar_hsa_circ_191979,RMVar_hsa_circ_75526,RMVar_hsa_circ_27472,RMVar_hsa_circ_342135,RMVar_hsa_circ_18272,RMVar_hsa_circ_268138,RMVar_hsa_circ_315794 24115 RMVar_ID_24115 Human_SNP_ID_657322677 A-to-I Human chr19 - 7479239 7479238 7479240 CCTCAGGTGATCCACCGGCCTTGGCCTCCCAAAGTCCCGGGATTACAGGTGTGAGCCATCGCGCT CCTCAGGTGATCCACCGGCCTTGGCCTCCCA__GTCCCGGGATTACAGGTGTGAGCCATCGCGCT CTT C PEX11G Ensembl:ENSG00000104883 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1490785779 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_107027,RMVar_hsa_circ_191985 24116 RMVar_ID_24116 Human_SNP_ID_657338656 A-to-I Human chr19 + 7532594 7532594 7532594 AAAAATTAGCGGACGTGGTGGCAGGCACCTGTAATCCCAGCTACTCCGGAGGCTGAGGCAGTAGA AAAAATTAGCGGACGTGGTGGCAGGCACCTGTGATCCCAGCTACTCCGGAGGCTGAGGCAGTAGA A G MCOLN1 Ensembl:ENSG00000090674 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1433753854 Functional Loss SNV dbSNP153 33..33 33 - - - 24117 RMVar_ID_24117 Human_SNP_ID_657338667 A-to-I Human chr19 + 7532647 7532647 7532647 TGAGGCAGTAGAATTGCTTGAACCTGGGACGTAGAGGTTGCAGTGAGCCGAGATCAAGCCACTGC TGAGGCAGTAGAATTGCTTGAACCTGGGACGTGGAGGTTGCAGTGAGCCGAGATCAAGCCACTGC A G MCOLN1 Ensembl:ENSG00000090674 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs535557825 Functional Loss SNV dbSNP153 33..33 33 - - - 24118 RMVar_ID_24118 Human_SNP_ID_657342813 A-to-I Human chr19 + 7545172 7545172 7545172 CCTCAGCCTCCCTCGAAGCTGGGACTACAGTCACGTGCCACCACGCCTGGCTAATTTTTGTAGTT CCTCAGCCTCCCTCGAAGCTGGGACTACAGTCCCGTGCCACCACGCCTGGCTAATTTTTGTAGTT A C PNPLA6 Ensembl:ENSG00000032444 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1418281896 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100653,RMVar_hsa_circ_110921,RMVar_hsa_circ_191992,RMVar_hsa_circ_328949,RMVar_hsa_circ_306263,RMVar_hsa_circ_191993,RMVar_hsa_circ_191994 24119 RMVar_ID_24119 Human_SNP_ID_657390167 A-to-I Human chr19 - 7693529 7693529 7693529 TTGCCCAGGCTGGTCTCAAACTCCTGGGCTCAAGCGATCCTCCTGCCTCAGCCTCCCAAGTAGCT TTGCCCAGGCTGGTCTCAAACTCCTGGGCTCAGGCGATCCTCCTGCCTCAGCCTCCCAAGTAGCT T C FCER2 Ensembl:ENSG00000104921 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1197118696 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102256,RMVar_hsa_circ_192022 24120 RMVar_ID_24120 Human_SNP_ID_657390330 A-to-I Human chr19 - 7694064 7694064 7694064 TGTGAGGGTGGGCGTGGTGGCTCACGCCTGTAATCCCAGCATTTTGGGAGGCCGAGGCAGGAGGA TGTGAGGGTGGGCGTGGTGGCTCACGCCTGTAGTCCCAGCATTTTGGGAGGCCGAGGCAGGAGGA T C FCER2 Ensembl:ENSG00000104921 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs187886673 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102256,RMVar_hsa_circ_192022 24121 RMVar_ID_24121 Human_SNP_ID_657390388 A-to-I Human chr19 - 7694282 7694282 7694282 TGGCTCACTACGGCCTCAAACTCCTGGGGTCAAGTGATCCTCTCATCTTGGCCTCCCAAATCGCT TGGCTCACTACGGCCTCAAACTCCTGGGGTCAGGTGATCCTCTCATCTTGGCCTCCCAAATCGCT T C FCER2 Ensembl:ENSG00000104921 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1015081289 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102256,RMVar_hsa_circ_192022 24122 RMVar_ID_24122 Human_SNP_ID_657390395 A-to-I Human chr19 - 7694305 7694305 7694305 GCTGGAGTGCAGTGGCACAATCATGGCTCACTACGGCCTCAAACTCCTGGGGTCAAGTGATCCTC GCTGGAGTGCAGTGGCACAATCATGGCTCACTGCGGCCTCAAACTCCTGGGGTCAAGTGATCCTC T C FCER2 Ensembl:ENSG00000104921 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1270287439 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102256,RMVar_hsa_circ_192022 24123 RMVar_ID_24123 Human_SNP_ID_657390532 A-to-I Human chr19 - 7694870 7694860 7694870 GGATTGAGCCACTGCACTCCAGCCTGGGCAACAGAGTGGGACCTTGCCTCTGAAGAAAAAAAAAA GGATTGAGCCACTGCACTCCAGCCTGGGCAAC__________CTTGCCTCTGAAGAAAAAAAAAA GGTCCCACTCT G FCER2 Ensembl:ENSG00000104921 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1428403204 Functional Loss DEL dbSNP153 33..42 33 - - - RMVar_hsa_circ_102256,RMVar_hsa_circ_192022 24124 RMVar_ID_24124 Human_SNP_ID_657390590 A-to-I Human chr19 - 7695117 7695117 7695117 TAATGTGGGGTAGGGACCAGGTGCACTGGCTCACGCCTATAGTCCCAGCACTTTGGGAGGCCGAG TAATGTGGGGTAGGGACCAGGTGCACTGGCTCCCGCCTATAGTCCCAGCACTTTGGGAGGCCGAG T G FCER2 Ensembl:ENSG00000104921 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs905387561 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102256,RMVar_hsa_circ_192022 24125 RMVar_ID_24125 Human_SNP_ID_657390675 A-to-I Human chr19 - 7695554 7695554 7695554 CCAGGCTGGTCCTGAACTCCTGGGCTCCAGCAATCCTCTCGCCTCGGCCTCCCAAAATGCTGAGA CCAGGCTGGTCCTGAACTCCTGGGCTCCAGCAGTCCTCTCGCCTCGGCCTCCCAAAATGCTGAGA T C FCER2 Ensembl:ENSG00000104921 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1442859233 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102256,RMVar_hsa_circ_192022 24126 RMVar_ID_24126 Human_SNP_ID_657390689 A-to-I Human chr19 - 7695604 7695604 7695604 CCCTAGCTAATTTTTTTATTTTTTGTAGCGACAGGATCTCGCTATGTTGCCCAGGCTGGTCCTGA CCCTAGCTAATTTTTTTATTTTTTGTAGCGACGGGATCTCGCTATGTTGCCCAGGCTGGTCCTGA T C FCER2 Ensembl:ENSG00000104921 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs972484925 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102256,RMVar_hsa_circ_192022 24127 RMVar_ID_24127 Human_SNP_ID_657390747 A-to-I Human chr19 - 7695805 7695805 7695805 TCAAGAGATCCTCCCACCTCAGCTTCCAGAGTAGCTGAGACTACGAGTGTGTGCCACCACGCCAG TCAAGAGATCCTCCCACCTCAGCTTCCAGAGTGGCTGAGACTACGAGTGTGTGCCACCACGCCAG T C FCER2 Ensembl:ENSG00000104921 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1457691395 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102256,RMVar_hsa_circ_192022 24128 RMVar_ID_24128 Human_SNP_ID_657391135 A-to-I Human chr19 - 7696916 7696916 7696916 GTCTCTGAGCACCGCCCCTTGTTGACTCCCCAAGAATTGAACGAGAGGAACGAAGCTTCAGATTT GTCTCTGAGCACCGCCCCTTGTTGACTCCCCAGGAATTGAACGAGAGGAACGAAGCTTCAGATTT T C FCER2 Ensembl:ENSG00000104921 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs189595510 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_Splice_Rec_1948215,Human_Splice_Rec_1948233,Human_Splice_Rec_1948253,Human_Splice_Rec_1948273,Human_Splice_Rec_1948291,Human_Splice_Rec_1948309,Human_Splice_Rec_1948325 RMVar_hsa_circ_102256,RMVar_hsa_circ_192022 24129 RMVar_ID_24129 Human_SNP_ID_657466344 A-to-I Human chr19 + 7945045 7945045 7945045 GCCCAAGAGTTTGAGACCAGCCTGGGCAACATAGTGAAGACCTCTTCTTTACAACAAATACAAAA GCCCAAGAGTTTGAGACCAGCCTGGGCAACATGGTGAAGACCTCTTCTTTACAACAAATACAAAA A G AC010336.8 Ensembl:ENSG00000286138 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1371660532 Functional Loss SNV dbSNP153 33..33 33 - - - 24130 RMVar_ID_24130 Human_SNP_ID_657466518 A-to-I Human chr19 + 7945682 7945681 7945683 GACCTCCATCTCTTTTTTTGTTGTTTTGAGACAGAGTCTCACTCTGTCGCCCAGGCTGGAGTGCA GACCTCCATCTCTTTTTTTGTTGTTTTGAGAC__AGTCTCACTCTGTCGCCCAGGCTGGAGTGCA CAG C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1239102381 Functional Loss DEL dbSNP153 33..34 33 - - - 24131 RMVar_ID_24131 Human_SNP_ID_657485568 A-to-I Human chr19 + 8015693 8015693 8015693 TCGCTGCATCCCCCAGGCTGGAGTACAGTGGTATGATCTTGGCTCACTGCAACCTCTGCCTCCTA TCGCTGCATCCCCCAGGCTGGAGTACAGTGGTGTGATCTTGGCTCACTGCAACCTCTGCCTCCTA A G AC008946.1 Ensembl:ENSG00000267939 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1028519449 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1949072 24132 RMVar_ID_24132 Human_SNP_ID_657543876 A-to-I Human chr19 + 8213560 8213560 8213560 GAACTCCTGGCCTCAAGCGAGCCTCCAGCCTCAACCTCCCAAAGCACTAGGATTATAGGCATGAG GAACTCCTGGCCTCAAGCGAGCCTCCAGCCTCGACCTCCCAAAGCACTAGGATTATAGGCATGAG A G CERS4 Ensembl:ENSG00000090661 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs77436451 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100557,RMVar_hsa_circ_91550,RMVar_hsa_circ_192076,RMVar_hsa_circ_192077 24133 RMVar_ID_24133 Human_SNP_ID_657545951 A-to-I Human chr19 + 8221169 8221169 8221169 TTTTTTTTTTTAAACAGAGACAGGGTCTCGCTATGTTGCTCAGGCTGGTCTTGAACTGCTAGGCT TTTTTTTTTTTAAACAGAGACAGGGTCTCGCTGTGTTGCTCAGGCTGGTCTTGAACTGCTAGGCT A G CERS4 Ensembl:ENSG00000090661 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1344616401 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22720413 RMVar_hsa_circ_100557,RMVar_hsa_circ_91550,RMVar_hsa_circ_192076,RMVar_hsa_circ_192077 24134 RMVar_ID_24134 Human_SNP_ID_657547355 A-to-I Human chr19 + 8226129 8226128 8226130 TGAGACGGGAGAATCGCTTGAATCCGGGAGGCAGAGGTTGCAGTGAGCCGAAGTCACACCACTGC TGAGACGGGAGAATCGCTTGAATCCGGGAGGC__AGGTTGCAGTGAGCCGAAGTCACACCACTGC CAG C CERS4 Ensembl:ENSG00000090661 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1174902409 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_100557,RMVar_hsa_circ_91550,RMVar_hsa_circ_192076,RMVar_hsa_circ_192077 24135 RMVar_ID_24135 Human_SNP_ID_657547356 A-to-I Human chr19 + 8226129 8226129 8226129 TGAGACGGGAGAATCGCTTGAATCCGGGAGGCAGAGGTTGCAGTGAGCCGAAGTCACACCACTGC TGAGACGGGAGAATCGCTTGAATCCGGGAGGCCGAGGTTGCAGTGAGCCGAAGTCACACCACTGC A C CERS4 Ensembl:ENSG00000090661 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1414740636 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100557,RMVar_hsa_circ_91550,RMVar_hsa_circ_192076,RMVar_hsa_circ_192077 24136 RMVar_ID_24136 Human_SNP_ID_657555148 A-to-I Human chr19 + 8252502 8252502 8252502 GCTCTTTCACCTTGGCTGGAGTACAGTGGCACAATCTCAGTTCACTACAACCTCTGCCTCCCAGG GCTCTTTCACCTTGGCTGGAGTACAGTGGCACCATCTCAGTTCACTACAACCTCTGCCTCCCAGG A C CERS4 Ensembl:ENSG00000090661 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1468842192 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117484,RMVar_hsa_circ_100557,RMVar_hsa_circ_91550,RMVar_hsa_circ_192076,RMVar_hsa_circ_192077,RMVar_hsa_circ_369071,RMVar_hsa_circ_192078 24137 RMVar_ID_24137 Human_SNP_ID_657557702 A-to-I Human chr19 + 8258761 8258761 8258761 CTACTCGGGAGGCTGAGGCAGGAGGATCACTTAAACCCAGAAGGCAGAGGCTACAGCGAATCAAG CTACTCGGGAGGCTGAGGCAGGAGGATCACTTGAACCCAGAAGGCAGAGGCTACAGCGAATCAAG A G CERS4 Ensembl:ENSG00000090661 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1255845801 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100360,RMVar_hsa_circ_192086 24138 RMVar_ID_24138 Human_SNP_ID_657560045 A-to-I Human chr19 + 8264892 8264892 8264892 TGAAACCCATCTCTACTAAAAATACAAAAATTAGCCGGGCATGGTGACACGTGCATGTAATCCCA TGAAACCCATCTCTACTAAAAATACAAAAATTGGCCGGGCATGGTGACACGTGCATGTAATCCCA A G lnc-CERS4-6 RNACentral:URS0000D59A57 lincRNA exon GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1039991789 Functional Loss SNV dbSNP153 33..33 33 - - - 24139 RMVar_ID_24139 Human_SNP_ID_657571460 A-to-I Human chr19 - 8312838 8312838 8312838 CAGCATGGGGAAACCCCATCTCTACAAAAAATACAAAAATTAGCCGGGTGTGGTGGTGTGCACCC CAGCATGGGGAAACCCCATCTCTACAAAAAATGCAAAAATTAGCCGGGTGTGGTGGTGTGCACCC T C AC010323.1,NDUFA7 Ensembl:ENSG00000167774,Ensembl:ENSG00000267855 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1430765360 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_300282 24140 RMVar_ID_24140 Human_SNP_ID_657571465 A-to-I Human chr19 - 8312853 8312853 8312853 CAAGACCAGCCTGAGCAGCATGGGGAAACCCCATCTCTACAAAAAATACAAAAATTAGCCGGGTG CAAGACCAGCCTGAGCAGCATGGGGAAACCCCGTCTCTACAAAAAATACAAAAATTAGCCGGGTG T C AC010323.1,NDUFA7 Ensembl:ENSG00000167774,Ensembl:ENSG00000267855 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1007530098 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_300282 24141 RMVar_ID_24141 Human_SNP_ID_657572272 A-to-I Human chr19 - 8315904 8315904 8315904 GTGATCCACCCGACTCGGCCTCCCAAAGTGCTAGGATTACAGGCGTGACCCACCGTGCCTGGCCT GTGATCCACCCGACTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGACCCACCGTGCCTGGCCT T C AC010323.1,NDUFA7 Ensembl:ENSG00000167774,Ensembl:ENSG00000267855 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs901164972 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_300282 24142 RMVar_ID_24142 Human_SNP_ID_657573286 A-to-I Human chr19 - 8319342 8319342 8319342 GTTGGCCAGTCTGGTCTCGAACTCCTGACTTCATAATCCGCCTGCCTCGGCCTCCCAAAGTGCTG GTTGGCCAGTCTGGTCTCGAACTCCTGACTTCGTAATCCGCCTGCCTCGGCCTCCCAAAGTGCTG T C AC010323.1,NDUFA7 Ensembl:ENSG00000167774,Ensembl:ENSG00000267855 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs9676507 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1949880,Human_Splice_Rec_1949881,Human_Splice_Rec_1949887 24143 RMVar_ID_24143 Human_SNP_ID_657573436 A-to-I Human chr19 - 8319878 8319878 8319878 TCGCACCACTGCACTCCAGCCTGGGTGACAGAACAACACTCTGTCTCAAAAAAATAAAAAAGAAA TCGCACCACTGCACTCCAGCCTGGGTGACAGAGCAACACTCTGTCTCAAAAAAATAAAAAAGAAA T C AC010323.1,NDUFA7 Ensembl:ENSG00000167774,Ensembl:ENSG00000267855 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1329989989 Functional Loss SNV dbSNP153 33..33 33 - - - 24144 RMVar_ID_24144 Human_SNP_ID_657580079 A-to-I Human chr19 - 8339445 8339445 8339445 TGAGGCAGGAGAATCACTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCCAAGATTGTGCCACTGC TGAGGCAGGAGAATCACTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCCAAGATTGTGCCACTGC T C KANK3 Ensembl:ENSG00000186994 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1481214336 Functional Loss SNV dbSNP153 33..33 33 - - - 24145 RMVar_ID_24145 Human_SNP_ID_657590878 A-to-I Human chr19 - 8374899 8374899 8374899 GAGCCTTCAGGGGTGGGTGCAGTGGCGCTCACACCTTTAATCCCATCACTTTGTGAAGCCAAGGC GAGCCTTCAGGGGTGGGTGCAGTGGCGCTCACCCCTTTAATCCCATCACTTTGTGAAGCCAAGGC T G RAB11B-AS1 Ensembl:ENSG00000269386 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1158078417 Functional Loss SNV dbSNP153 33..33 33 - - - 24146 RMVar_ID_24146 Human_SNP_ID_657599945 A-to-I Human chr19 + 8405523 8405523 8405523 TCAAGGGATTCTCCTGCCTCAGCCTCTGGAGTAGCTGGGATTACAGGCACATGCGACCACACCCA TCAAGGGATTCTCCTGCCTCAGCCTCTGGAGTGGCTGGGATTACAGGCACATGCGACCACACCCA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1294787080 Functional Loss SNV dbSNP153 33..33 33 - - - 24147 RMVar_ID_24147 Human_SNP_ID_657602427 A-to-I Human chr19 + 8413723 8413723 8413723 AGGAGGTGGCTGGTGCAGAAAACGCCTGACACACAGTAGGCAACTGCTAAGTGGCCAATGCCCTT AGGAGGTGGCTGGTGCAGAAAACGCCTGACACGCAGTAGGCAACTGCTAAGTGGCCAATGCCCTT A G MARCHF2 Ensembl:ENSG00000099785 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1284326244 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1950119 24148 RMVar_ID_24148 Human_SNP_ID_657603766 A-to-I Human chr19 + 8418602 8418602 8418602 GCTGGAGTGCAGTGGTGTGATCATAGCTCACTACAGCCTTGAACTCCTGGGCTCAAGAGGTTGAG GCTGGAGTGCAGTGGTGTGATCATAGCTCACTGCAGCCTTGAACTCCTGGGCTCAAGAGGTTGAG A G MARCHF2 Ensembl:ENSG00000099785 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1043253882 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1950096,Human_Splice_Rec_1950116,Human_Splice_Rec_1950120 24149 RMVar_ID_24149 Human_SNP_ID_657606892 A-to-I Human chr19 + 8428565 8428565 8428565 CCAGCTACTTGGGAGGCTGAGGCAGGAGAATCACTTAAAGCTGGGAGGCGGAGTTTGCAGTGAGT CCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTAAAGCTGGGAGGCGGAGTTTGCAGTGAGT A G MARCHF2 Ensembl:ENSG00000099785 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs541819083 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_348680,RMVar_hsa_circ_192105,RMVar_hsa_circ_349551,RMVar_hsa_circ_192107 24150 RMVar_ID_24150 Human_SNP_ID_657607179 A-to-I Human chr19 + 8429384 8429384 8429384 TCATGCCTGTAATCCCAGCACTTTGGGAAGCCAAGGTGGGAAGATCACTTGAGGCCAGGAGTTCA TCATGCCTGTAATCCCAGCACTTTGGGAAGCCGAGGTGGGAAGATCACTTGAGGCCAGGAGTTCA A G MARCHF2 Ensembl:ENSG00000099785 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1355514539 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_348680,RMVar_hsa_circ_192105,RMVar_hsa_circ_349551,RMVar_hsa_circ_192107 24151 RMVar_ID_24151 Human_SNP_ID_657608508 A-to-I Human chr19 + 8434294 8434294 8434294 TTTAGTAGAGACGGGGTTTCGCCATGTTGGCCAGGCTGGTCTCGAACTCTTGACCTCAGGTATCC TTTAGTAGAGACGGGGTTTCGCCATGTTGGCCGGGCTGGTCTCGAACTCTTGACCTCAGGTATCC A G MARCHF2 Ensembl:ENSG00000099785 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1245306164 Functional Loss SNV dbSNP153 33..33 33 - - - 24152 RMVar_ID_24152 Human_SNP_ID_657608908 A-to-I Human chr19 + 8435803 8435803 8435803 CTCAAACCTTGGCTTCCCAGAGTGCTGGGATTATAGGTGTGAGCCACTGCACCTGGCCTGTGTGT CTCAAACCTTGGCTTCCCAGAGTGCTGGGATTGTAGGTGTGAGCCACTGCACCTGGCCTGTGTGT A G MARCHF2 Ensembl:ENSG00000099785 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1212385196 Functional Loss SNV dbSNP153 33..33 33 - - - 24153 RMVar_ID_24153 Human_SNP_ID_657612559 A-to-I Human chr19 + 8447905 8447905 8447905 AAAATTAGCCGGGCGTGGTGCCGGGCTCCTGTAGTCTCAGCCACTGGGGAGGCTGAGGCAGGAGA AAAATTAGCCGGGCGTGGTGCCGGGCTCCTGTGGTCTCAGCCACTGGGGAGGCTGAGGCAGGAGA A G HNRNPM Ensembl:ENSG00000099783 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946777055 Functional Loss SNV dbSNP153 33..33 33 - - - 24154 RMVar_ID_24154 Human_SNP_ID_657619568 A-to-I Human chr19 + 8473108 8473108 8473108 TCCATCTCTACAAAATATAAAAAAAATCAGCCAGGTGTGGTGGCGTAGTCCCAGCTACTTGGGAG TCCATCTCTACAAAATATAAAAAAAATCAGCCCGGTGTGGTGGCGTAGTCCCAGCTACTTGGGAG A C HNRNPM Ensembl:ENSG00000099783 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs373579118 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_307845,RMVar_hsa_circ_266612,RMVar_hsa_circ_192112,RMVar_hsa_circ_292107,RMVar_hsa_circ_192116,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 24155 RMVar_ID_24155 Human_SNP_ID_657619569 A-to-I Human chr19 + 8473108 8473108 8473108 TCCATCTCTACAAAATATAAAAAAAATCAGCCAGGTGTGGTGGCGTAGTCCCAGCTACTTGGGAG TCCATCTCTACAAAATATAAAAAAAATCAGCCGGGTGTGGTGGCGTAGTCCCAGCTACTTGGGAG A G HNRNPM Ensembl:ENSG00000099783 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs373579118 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_307845,RMVar_hsa_circ_266612,RMVar_hsa_circ_192112,RMVar_hsa_circ_292107,RMVar_hsa_circ_192116,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 24156 RMVar_ID_24156 Human_SNP_ID_657619570 A-to-I Human chr19 + 8473108 8473108 8473108 TCCATCTCTACAAAATATAAAAAAAATCAGCCAGGTGTGGTGGCGTAGTCCCAGCTACTTGGGAG TCCATCTCTACAAAATATAAAAAAAATCAGCCTGGTGTGGTGGCGTAGTCCCAGCTACTTGGGAG A T HNRNPM Ensembl:ENSG00000099783 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs373579118 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_307845,RMVar_hsa_circ_266612,RMVar_hsa_circ_192112,RMVar_hsa_circ_292107,RMVar_hsa_circ_192116,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 24157 RMVar_ID_24157 Human_SNP_ID_657620361 A-to-I Human chr19 + 8475877 8475877 8475877 ATTGCTTGAGCTCAGGAGTTCAAGATCAGCCTAGGCAACACTGCGAAACCCCATCTCTCTCTTTT ATTGCTTGAGCTCAGGAGTTCAAGATCAGCCTGGGCAACACTGCGAAACCCCATCTCTCTCTTTT A G HNRNPM Ensembl:ENSG00000099783 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1235045397 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25439720 RMVar_hsa_circ_266612,RMVar_hsa_circ_334894,RMVar_hsa_circ_192124 24158 RMVar_ID_24158 Human_SNP_ID_657620781 A-to-I Human chr19 + 8477121 8477121 8477121 GTATAATGCAAGGTGTTCATTACATCGCACCTATCTTACCTGACATTTCTAAGGAGTGAGATGAT GTATAATGCAAGGTGTTCATTACATCGCACCTGTCTTACCTGACATTTCTAAGGAGTGAGATGAT A G HNRNPM Ensembl:ENSG00000099783 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7408960 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2306,GWAS_ID_2307 RMVar_hsa_circ_266612,RMVar_hsa_circ_334894,RMVar_hsa_circ_192124 24159 RMVar_ID_24159 Human_SNP_ID_657621440 A-to-I Human chr19 + 8479160 8479160 8479160 CAGGCTGGAGTGCAATGGTGCGATCTCAGCTCACTGCGGCCTCCACCTCCCGGTTTCAAGTGGTT CAGGCTGGAGTGCAATGGTGCGATCTCAGCTCGCTGCGGCCTCCACCTCCCGGTTTCAAGTGGTT A G HNRNPM Ensembl:ENSG00000099783 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005356260 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266612,RMVar_hsa_circ_334894,RMVar_hsa_circ_192124 24160 RMVar_ID_24160 Human_SNP_ID_657621554 A-to-I Human chr19 + 8479637 8479636 8479638 CATGCCCAGCTAATTTATTTTTTTGTAGAGACAGAGTGTATGTTGCCCAGGCTTATTACAAATTC CATGCCCAGCTAATTTATTTTTTTGTAGAGAC__AGTGTATGTTGCCCAGGCTTATTACAAATTC CAG C HNRNPM Ensembl:ENSG00000099783 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1172040541 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_13537510,Human_RBP_ID_17568376,Human_RBP_ID_23812013 RMVar_hsa_circ_266612,RMVar_hsa_circ_334894,RMVar_hsa_circ_192124 24161 RMVar_ID_24161 Human_SNP_ID_657621555 A-to-I Human chr19 + 8479637 8479637 8479637 CATGCCCAGCTAATTTATTTTTTTGTAGAGACAGAGTGTATGTTGCCCAGGCTTATTACAAATTC CATGCCCAGCTAATTTATTTTTTTGTAGAGACGGAGTGTATGTTGCCCAGGCTTATTACAAATTC A G HNRNPM Ensembl:ENSG00000099783 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs543980371 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13537510,Human_RBP_ID_17568376,Human_RBP_ID_23812013 RMVar_hsa_circ_266612,RMVar_hsa_circ_334894,RMVar_hsa_circ_192124 24162 RMVar_ID_24162 Human_SNP_ID_657621660 A-to-I Human chr19 + 8479914 8479914 8479914 TCTCTGCCTCAGCCTCCAGAGTAGCTGGGATTACAGGCGCGTGCCCCCATGTCCGGCTAATTTTT TCTCTGCCTCAGCCTCCAGAGTAGCTGGGATTGCAGGCGCGTGCCCCCATGTCCGGCTAATTTTT A G HNRNPM Ensembl:ENSG00000099783 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1299666938 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266612,RMVar_hsa_circ_334894,RMVar_hsa_circ_192124 24163 RMVar_ID_24163 Human_SNP_ID_657621864 A-to-I Human chr19 + 8480595 8480595 8480595 GGCTGAGGCAGAATTGCTTGAACCTGGGAGGTAGAGGTTGCAGTGAGCCGAGATGACACCACTGC GGCTGAGGCAGAATTGCTTGAACCTGGGAGGTGGAGGTTGCAGTGAGCCGAGATGACACCACTGC A G HNRNPM Ensembl:ENSG00000099783 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1247745484 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266612,RMVar_hsa_circ_334894,RMVar_hsa_circ_192124 24164 RMVar_ID_24164 Human_SNP_ID_657621866 A-to-I Human chr19 + 8480613 8480610 8480614 TGAACCTGGGAGGTAGAGGTTGCAGTGAGCCGAGATGACACCACTGCACTCTAGCCTGGGCGACA TGAACCTGGGAGGTAGAGGTTGCAGTGAGC____ATGACACCACTGCACTCTAGCCTGGGCGACA CCGAG C HNRNPM Ensembl:ENSG00000099783 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1051885726 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_25439756 RMVar_hsa_circ_266612,RMVar_hsa_circ_334894,RMVar_hsa_circ_192124 24165 RMVar_ID_24165 Human_SNP_ID_657621879 A-to-I Human chr19 + 8480645 8480644 8480646 AGATGACACCACTGCACTCTAGCCTGGGCGACAGAGTGAGACTCTGTCTCAAAATTAAAAAAAAA AGATGACACCACTGCACTCTAGCCTGGGCGAC__AGTGAGACTCTGTCTCAAAATTAAAAAAAAA CAG C HNRNPM Ensembl:ENSG00000099783 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1394765321 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_266612,RMVar_hsa_circ_334894,RMVar_hsa_circ_192124 24166 RMVar_ID_24166 Human_SNP_ID_657827794 A-to-I Human chr19 + 9149349 9149349 9149349 TACAAAAATTAGCCGGACACAGTGGCACACCTATAGTCCCAGCTACTTGGGAGCCTGAGGCGGGA TACAAAAATTAGCCGGACACAGTGGCACACCTGTAGTCCCAGCTACTTGGGAGCCTGAGGCGGGA A G ZNF317 Ensembl:ENSG00000130803 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1230908592 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25439954 24167 RMVar_ID_24167 Human_SNP_ID_657827796 A-to-I Human chr19 + 9149351 9149351 9149351 CAAAAATTAGCCGGACACAGTGGCACACCTATAGTCCCAGCTACTTGGGAGCCTGAGGCGGGAGA CAAAAATTAGCCGGACACAGTGGCACACCTATGGTCCCAGCTACTTGGGAGCCTGAGGCGGGAGA A G ZNF317 Ensembl:ENSG00000130803 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs966079306 Functional Loss SNV dbSNP153 33..33 33 - - - 24168 RMVar_ID_24168 Human_SNP_ID_657873516 A-to-I Human chr19 + 9325515 9325515 9325515 TGTAGCTCGAGTAAAACAAATGTCTTTAGTCCAGGTGTGGTGGCTCACGCCTGTAATCCCAGCAT TGTAGCTCGAGTAAAACAAATGTCTTTAGTCCGGGTGTGGTGGCTCACGCCTGTAATCCCAGCAT A G ZNF559,ZNF559-ZNF177 Ensembl:ENSG00000188321,Ensembl:ENSG00000270011 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1051428882 Functional Loss SNV dbSNP153 33..33 33 - - - 24169 RMVar_ID_24169 Human_SNP_ID_657873517 A-to-I Human chr19 + 9325515 9325515 9325515 TGTAGCTCGAGTAAAACAAATGTCTTTAGTCCAGGTGTGGTGGCTCACGCCTGTAATCCCAGCAT TGTAGCTCGAGTAAAACAAATGTCTTTAGTCCTGGTGTGGTGGCTCACGCCTGTAATCCCAGCAT A T ZNF559,ZNF559-ZNF177 Ensembl:ENSG00000188321,Ensembl:ENSG00000270011 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1051428882 Functional Loss SNV dbSNP153 33..33 33 - - - 24170 RMVar_ID_24170 Human_SNP_ID_657875756 A-to-I Human chr19 + 9333064 9333064 9333064 AGATCACGGTTCACTGCAGCATTGACCTCCCTAGGCTCAGGTGTTGCTCCCACCTCAGTCTTCTG AGATCACGGTTCACTGCAGCATTGACCTCCCTGGGCTCAGGTGTTGCTCCCACCTCAGTCTTCTG A G ZNF559,ZNF559-ZNF177 Ensembl:ENSG00000188321,Ensembl:ENSG00000270011 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs147148417 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1951656,Human_Splice_Rec_1951657,Human_Splice_Rec_1951688,Human_Splice_Rec_1951689,Human_Splice_Rec_1951764,Human_Splice_Rec_1951765 24171 RMVar_ID_24171 Human_SNP_ID_657876396 A-to-I Human chr19 + 9335235 9335235 9335235 AAGGCGGGAGGATCGCTTGAGCCCAGGAGTTCAAGATCAGCCTTTCCAACATTGCGAGGAACCCC AAGGCGGGAGGATCGCTTGAGCCCAGGAGTTCGAGATCAGCCTTTCCAACATTGCGAGGAACCCC A G ZNF559,ZNF559-ZNF177 Ensembl:ENSG00000188321,Ensembl:ENSG00000270011 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs530436438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241954 24172 RMVar_ID_24172 Human_SNP_ID_657879414 A-to-I Human chr19 + 9344123 9344123 9344123 AAAATTAGCCAGGCATGGTGGTACGTGCCTGTAATCCCAGCTACTCGAGAGGTTGAGGCAGAATT AAAATTAGCCAGGCATGGTGGTACGTGCCTGTCATCCCAGCTACTCGAGAGGTTGAGGCAGAATT A C ZNF559,ZNF559-ZNF177 Ensembl:ENSG00000188321,Ensembl:ENSG00000270011 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1009010264 Functional Loss SNV dbSNP153 33..33 33 - - - 24173 RMVar_ID_24173 Human_SNP_ID_657879421 A-to-I Human chr19 + 9344133 9344133 9344133 AGGCATGGTGGTACGTGCCTGTAATCCCAGCTACTCGAGAGGTTGAGGCAGAATTGCTTGAACCC AGGCATGGTGGTACGTGCCTGTAATCCCAGCTGCTCGAGAGGTTGAGGCAGAATTGCTTGAACCC A G ZNF559,ZNF559-ZNF177 Ensembl:ENSG00000188321,Ensembl:ENSG00000270011 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs972498019 Functional Loss SNV dbSNP153 33..33 33 - - - 24174 RMVar_ID_24174 Human_SNP_ID_657899864 A-to-I Human chr19 - 9415988 9415988 9415988 GAAATCTCGTCTCTACTAAAAATACAAAAATTAGCTGGGCGTTGTGGCATGTGCCTGTAGTCCCA GAAATCTCGTCTCTACTAAAAATACAAAAATTGGCTGGGCGTTGTGGCATGTGCCTGTAGTCCCA T C ZNF266 Ensembl:ENSG00000174652 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1436117887 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_192199,RMVar_hsa_circ_102667,RMVar_hsa_circ_192201,RMVar_hsa_circ_348655,RMVar_hsa_circ_376310,RMVar_hsa_circ_293107,RMVar_hsa_circ_192200 24175 RMVar_ID_24175 Human_SNP_ID_657900065 A-to-I Human chr19 - 9416567 9416567 9416567 CTGATGTCAGGAGTTCGAGACCAGCATGGCCAACATGCTGAAACCCTGTCTCTACTAAAAATGCA CTGATGTCAGGAGTTCGAGACCAGCATGGCCAGCATGCTGAAACCCTGTCTCTACTAAAAATGCA T C ZNF266 Ensembl:ENSG00000174652 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1276001113 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_192199,RMVar_hsa_circ_102667,RMVar_hsa_circ_192201,RMVar_hsa_circ_348655,RMVar_hsa_circ_376310,RMVar_hsa_circ_293107,RMVar_hsa_circ_192200 24176 RMVar_ID_24176 Human_SNP_ID_657900302 A-to-I Human chr19 - 9417304 9417304 9417304 GCAGTGGTGCGATCTCGGCTTACTGCAACTTCAGCCTCCCGGGTTCAGGTAATTCTCCTGAGTAC GCAGTGGTGCGATCTCGGCTTACTGCAACTTCCGCCTCCCGGGTTCAGGTAATTCTCCTGAGTAC T G ZNF266 Ensembl:ENSG00000174652 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1036102999 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_192199,RMVar_hsa_circ_102667,RMVar_hsa_circ_192201,RMVar_hsa_circ_348655,RMVar_hsa_circ_376310,RMVar_hsa_circ_293107,RMVar_hsa_circ_192200 24177 RMVar_ID_24177 Human_SNP_ID_657904694 A-to-I Human chr19 - 9433788 9433786 9433788 AATTTTTGTATTTTTGTATTTTTTTTTTTTTTAGTAGAGATGGTTTCAGCATGTTGGCCAGTCTG AATTTTTGTATTTTTGTATTTTTTTTTTTTTT__TAGAGATGGTTTCAGCATGTTGGCCAGTCTG ACT A ZNF266 Ensembl:ENSG00000174652 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1287188524 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_110059,RMVar_hsa_circ_192207 24178 RMVar_ID_24178 Human_SNP_ID_657929005 A-to-I Human chr19 - 9524721 9524721 9524721 GCTGGAGTGCAATGGCTCAATCTTGGCTCACTACAACCTCTATCACCCAGGTTCAAGTGATTATT GCTGGAGTGCAATGGCTCAATCTTGGCTCACTGCAACCTCTATCACCCAGGTTCAAGTGATTATT T C ZNF426 Ensembl:ENSG00000130818 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1472404988 Functional Loss SNV dbSNP153 33..33 33 - - - 24179 RMVar_ID_24179 Human_SNP_ID_657931234 A-to-I Human chr19 - 9532473 9532473 9532473 GGCAACATACCGAGAACCTTGTTTCTACAAAAAATACAAAAATTAGCCGAGGGTGGTGGGACGCA GGCAACATACCGAGAACCTTGTTTCTACAAAAGATACAAAAATTAGCCGAGGGTGGTGGGACGCA T C ZNF426 Ensembl:ENSG00000130818 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs986053431 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_192209,RMVar_hsa_circ_120028,RMVar_hsa_circ_271754,RMVar_hsa_circ_192210 24180 RMVar_ID_24180 Human_SNP_ID_657931266 A-to-I Human chr19 - 9532592 9532592 9532592 TGGTCCAAAAATATTAAATGGGAAACTCGGCCAGGCATGGTGGCCCACACCTGTAATCCCCACAC TGGTCCAAAAATATTAAATGGGAAACTCGGCCTGGCATGGTGGCCCACACCTGTAATCCCCACAC T A ZNF426 Ensembl:ENSG00000130818 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1273004964 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_192209,RMVar_hsa_circ_120028,RMVar_hsa_circ_271754,RMVar_hsa_circ_192210 24181 RMVar_ID_24181 Human_SNP_ID_657939380 A-to-I Human chr19 - 9561636 9561636 9561636 GCAGTCCTCCTGCCTCAGCCTCCCAAAGTGCCAGGATTACAGGTGTGAGCCACCACACCCAGTCC GCAGTCCTCCTGCCTCAGCCTCCCAAAGTGCCGGGATTACAGGTGTGAGCCACCACACCCAGTCC T C ZNF121 Ensembl:ENSG00000197961 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1339472372 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_141201 24182 RMVar_ID_24182 Human_SNP_ID_657939388 A-to-I Human chr19 - 9561670 9561670 9561670 GTTGCCCAGACTGGTCTCAAGCTCTTGGGCTCAAGCAGTCCTCCTGCCTCAGCCTCCCAAAGTGC GTTGCCCAGACTGGTCTCAAGCTCTTGGGCTCGAGCAGTCCTCCTGCCTCAGCCTCCCAAAGTGC T C ZNF121 Ensembl:ENSG00000197961 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1007681153 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241973 24183 RMVar_ID_24183 Human_SNP_ID_657939398 A-to-I Human chr19 - 9561704 9561702 9561704 AATTTTTTTATTCGTAGAGCCGAGGTCTCACTATGTTGCCCAGACTGGTCTCAAGCTCTTGGGCT AATTTTTTTATTCGTAGAGCCGAGGTCTCACT__GTTGCCCAGACTGGTCTCAAGCTCTTGGGCT CAT C ZNF121 Ensembl:ENSG00000197961 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1196883247 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_241973,Human_RBP_ID_774100,Human_RBP_ID_6795931,Human_RBP_ID_13540429,Human_RBP_ID_17936716,Human_RBP_ID_25440256,Human_RBP_ID_27280727 24184 RMVar_ID_24184 Human_SNP_ID_657939399 A-to-I Human chr19 - 9561704 9561704 9561704 AATTTTTTTATTCGTAGAGCCGAGGTCTCACTATGTTGCCCAGACTGGTCTCAAGCTCTTGGGCT AATTTTTTTATTCGTAGAGCCGAGGTCTCACTGTGTTGCCCAGACTGGTCTCAAGCTCTTGGGCT T C ZNF121 Ensembl:ENSG00000197961 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1274476696 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241973,Human_RBP_ID_774100,Human_RBP_ID_6795931,Human_RBP_ID_13540429,Human_RBP_ID_17936716,Human_RBP_ID_25440256,Human_RBP_ID_27280727 24185 RMVar_ID_24185 Human_SNP_ID_657939446 A-to-I Human chr19 - 9561860 9561860 9561860 TTGGTCTGCATTGGGGTCTTGCTCTGTTGCCTAGGGTGTGGAGTGCGGTGGCATGATCATGCCTC TTGGTCTGCATTGGGGTCTTGCTCTGTTGCCTGGGGTGTGGAGTGCGGTGGCATGATCATGCCTC T C ZNF121 Ensembl:ENSG00000197961 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1271262996 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241974,Human_RBP_ID_530028,Human_RBP_ID_772817,Human_RBP_ID_1019381,Human_RBP_ID_1374719,Human_RBP_ID_1575023,Human_RBP_ID_4556417,Human_RBP_ID_6795941,Human_RBP_ID_8497324,Human_RBP_ID_8838741,Human_RBP_ID_13540439,Human_RBP_ID_17934486,Human_RBP_ID_18742736,Human_RBP_ID_20435931,Human_RBP_ID_22391411,Human_RBP_ID_23812614,Human_RBP_ID_27684793 24186 RMVar_ID_24186 Human_SNP_ID_657939573 A-to-I Human chr19 - 9562276 9562276 9562276 CCTATAGTCCCAGCTATTCAGGAGGCTGAGGCAGGAGAATCACTTGAATCCAGGAGGTGGAGGTT CCTATAGTCCCAGCTATTCAGGAGGCTGAGGCGGGAGAATCACTTGAATCCAGGAGGTGGAGGTT T C ZNF121 Ensembl:ENSG00000197961 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs938094053 Functional Loss SNV dbSNP153 33..33 33 - - - 24187 RMVar_ID_24187 Human_SNP_ID_657939580 A-to-I Human chr19 - 9562303 9562302 9562304 AAAATTAGCCGGGCATGGTGGCAGGCACCTATAGTCCCAGCTATTCAGGAGGCTGAGGCAGGAGA AAAATTAGCCGGGCATGGTGGCAGGCACCTA__GTCCCAGCTATTCAGGAGGCTGAGGCAGGAGA CTA C ZNF121 Ensembl:ENSG00000197961 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1231067600 Functional Loss DEL dbSNP153 32..33 33 - - - 24188 RMVar_ID_24188 Human_SNP_ID_657939581 A-to-I Human chr19 - 9562305 9562305 9562305 AAAAAATTAGCCGGGCATGGTGGCAGGCACCTATAGTCCCAGCTATTCAGGAGGCTGAGGCAGGA AAAAAATTAGCCGGGCATGGTGGCAGGCACCTGTAGTCCCAGCTATTCAGGAGGCTGAGGCAGGA T C ZNF121 Ensembl:ENSG00000197961 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,31158229,31158229,31158229 RNA-Seq:(High) rs779110569 Functional Loss SNV dbSNP153 33..33 33 - - - 24189 RMVar_ID_24189 Human_SNP_ID_657939619 A-to-I Human chr19 - 9562437 9562437 9562437 CAGAGCAGCCGGGCACGGTGGCTCACACCTGTAATCCCAGCACCTTGAGAGGCTGAGGTGAGTGA CAGAGCAGCCGGGCACGGTGGCTCACACCTGTGATCCCAGCACCTTGAGAGGCTGAGGTGAGTGA T C ZNF121 Ensembl:ENSG00000197961 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1022205838 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6795962,Human_RBP_ID_13540472,Human_RBP_ID_23181380,Human_RBP_ID_23310069 24190 RMVar_ID_24190 Human_SNP_ID_657939791 A-to-I Human chr19 - 9562996 9562982 9562996 GGCTGGAGTGTAGTACAGTTATAGCCCATTGCAGCCTCAAACTTACGGGTTCCAGTGATCTTCCT GGCTGGAGTGTAGTACAGTTATAGCCCATTGC______________GGGTTCCAGTGATCTTCCT CGTAAGTTTGAGGCT C ZNF121 Ensembl:ENSG00000197961 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1568496150 Functional Loss DEL dbSNP153 33..46 33 - - - Human_RBP_ID_2572987,Human_RBP_ID_6795989,Human_RBP_ID_13540522,Human_RBP_ID_27684801 24191 RMVar_ID_24191 Human_SNP_ID_657940498 A-to-I Human chr19 - 9565561 9565561 9565561 CCTGGGTTCAGGCGATTCTGCCTCAGCCTTCAAGTAGCTTGGATTACAGGTGCCGTCAACCACAC CCTGGGTTCAGGCGATTCTGCCTCAGCCTTCACGTAGCTTGGATTACAGGTGCCGTCAACCACAC T G ZNF121 Ensembl:ENSG00000197961 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947050460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_530083,Human_RBP_ID_774103,Human_RBP_ID_6796095,Human_RBP_ID_8497339,Human_RBP_ID_13540712 RMVar_hsa_circ_192216 24192 RMVar_ID_24192 Human_SNP_ID_657940514 A-to-I Human chr19 - 9565609 9565609 9565609 CAGGCTGGAGTGCAATGGCATGATCCCAGCTCACTGCAACCTTTGTCTCCTGGGTTCAGGCGATT CAGGCTGGAGTGCAATGGCATGATCCCAGCTCGCTGCAACCTTTGTCTCCTGGGTTCAGGCGATT T C ZNF121 Ensembl:ENSG00000197961 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs890311100 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_530086,Human_RBP_ID_3579453,Human_RBP_ID_6796095,Human_RBP_ID_13540716,Human_RBP_ID_26998159 RMVar_hsa_circ_192216 24193 RMVar_ID_24193 Human_SNP_ID_657942732 A-to-I Human chr19 - 9573985 9573985 9573985 AAAATTAGCCAGGCATTGTGGTGCACATTTGTAGTAACAGTTACTTGGGAGGCTGATGTGAGAGT AAAATTAGCCAGGCATTGTGGTGCACATTTGTGGTAACAGTTACTTGGGAGGCTGATGTGAGAGT T C ZNF121 Ensembl:ENSG00000197961 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs570763860 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13540890,Human_RBP_ID_20431056 24194 RMVar_ID_24194 Human_SNP_ID_657944975 A-to-I Human chr19 - 9582673 9582673 9582673 GCGATCTCGGCTCACTGCAACCTCTGCCTCCCAGGTTCAAGTAATTCTCCTGCCTCCCTAGCATT GCGATCTCGGCTCACTGCAACCTCTGCCTCCCGGGTTCAAGTAATTCTCCTGCCTCCCTAGCATT T C ZNF121 Ensembl:ENSG00000197961 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs575761089 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23310070 24195 RMVar_ID_24195 Human_SNP_ID_657944999 A-to-I Human chr19 - 9582743 9582743 9582743 TCTAGTAGTTTTTTTTTTTTTTTTTTTGAGACAGAGTCTCGCTCTGCTACCCGGGTCGGGGTGCA TCTAGTAGTTTTTTTTTTTTTTTTTTTGAGACGGAGTCTCGCTCTGCTACCCGGGTCGGGGTGCA T C ZNF121 Ensembl:ENSG00000197961 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1057264157 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13541136 24196 RMVar_ID_24196 Human_SNP_ID_657954686 A-to-I Human chr19 - 9614566 9614566 9614566 AAGTCTTGCTCTGTCACCCAGGCTGGAGTGCAATGGCATGATCTCAGCTCACTGCAACTTCTGCC AAGTCTTGCTCTGTCACCCAGGCTGGAGTGCAGTGGCATGATCTCAGCTCACTGCAACTTCTGCC T C ZNF561 Ensembl:ENSG00000171469 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1225195466 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20435938 RMVar_hsa_circ_127779,RMVar_hsa_circ_125881,RMVar_hsa_circ_296937,RMVar_hsa_circ_192222,RMVar_hsa_circ_310289,RMVar_hsa_circ_296240,RMVar_hsa_circ_192223,RMVar_hsa_circ_192224 24197 RMVar_ID_24197 Human_SNP_ID_657954687 A-to-I Human chr19 - 9614566 9614566 9614566 AAGTCTTGCTCTGTCACCCAGGCTGGAGTGCAATGGCATGATCTCAGCTCACTGCAACTTCTGCC AAGTCTTGCTCTGTCACCCAGGCTGGAGTGCACTGGCATGATCTCAGCTCACTGCAACTTCTGCC T G ZNF561 Ensembl:ENSG00000171469 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1225195466 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20435938 RMVar_hsa_circ_127779,RMVar_hsa_circ_125881,RMVar_hsa_circ_296937,RMVar_hsa_circ_192222,RMVar_hsa_circ_310289,RMVar_hsa_circ_296240,RMVar_hsa_circ_192223,RMVar_hsa_circ_192224 24198 RMVar_ID_24198 Human_SNP_ID_657954791 A-to-I Human chr19 - 9614967 9614967 9614967 AGACGTGGTGGCACACGCCTTTAGTCCCAGCTAGTCAAGAGGCTGAGGCAGGAGAATCACTTCAA AGACGTGGTGGCACACGCCTTTAGTCCCAGCTGGTCAAGAGGCTGAGGCAGGAGAATCACTTCAA T C ZNF561 Ensembl:ENSG00000171469 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1000527884 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127779,RMVar_hsa_circ_125881,RMVar_hsa_circ_296937,RMVar_hsa_circ_192222,RMVar_hsa_circ_310289,RMVar_hsa_circ_296240,RMVar_hsa_circ_192223,RMVar_hsa_circ_192224 24199 RMVar_ID_24199 Human_SNP_ID_657954794 A-to-I Human chr19 - 9614977 9614977 9614977 AAAATTAGCCAGACGTGGTGGCACACGCCTTTAGTCCCAGCTAGTCAAGAGGCTGAGGCAGGAGA AAAATTAGCCAGACGTGGTGGCACACGCCTTTGGTCCCAGCTAGTCAAGAGGCTGAGGCAGGAGA T C ZNF561 Ensembl:ENSG00000171469 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1431070765 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127779,RMVar_hsa_circ_125881,RMVar_hsa_circ_296937,RMVar_hsa_circ_192222,RMVar_hsa_circ_310289,RMVar_hsa_circ_296240,RMVar_hsa_circ_192223,RMVar_hsa_circ_192224 24200 RMVar_ID_24200 Human_SNP_ID_657954877 A-to-I Human chr19 - 9615346 9615346 9615346 ATGATCCACCCACCTCGACCTCCCAAAGTGTTAGGATTACAGGCATGAGCCACCACACCCAGCCT ATGATCCACCCACCTCGACCTCCCAAAGTGTTGGGATTACAGGCATGAGCCACCACACCCAGCCT T C ZNF561 Ensembl:ENSG00000171469 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1263005100 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127779,RMVar_hsa_circ_125881,RMVar_hsa_circ_296937,RMVar_hsa_circ_192222,RMVar_hsa_circ_310289,RMVar_hsa_circ_296240,RMVar_hsa_circ_192223,RMVar_hsa_circ_192224 24201 RMVar_ID_24201 Human_SNP_ID_657954929 A-to-I Human chr19 - 9615515 9615515 9615515 CTGTTTACTACAACCTCTGCCCTCCCAGGTTCAGGTGATTCTCCTGCCTCAGCCTCCTGAGTAGC CTGTTTACTACAACCTCTGCCCTCCCAGGTTCGGGTGATTCTCCTGCCTCAGCCTCCTGAGTAGC T C ZNF561 Ensembl:ENSG00000171469 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1220290078 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127779,RMVar_hsa_circ_125881,RMVar_hsa_circ_296937,RMVar_hsa_circ_192222,RMVar_hsa_circ_310289,RMVar_hsa_circ_296240,RMVar_hsa_circ_192223,RMVar_hsa_circ_192224 24202 RMVar_ID_24202 Human_SNP_ID_657955033 A-to-I Human chr19 - 9615858 9615858 9615858 TTGAGACAGAGTCTCACTCCATCACCCAGGCTAGAGTGTAATGGTGCCACCTCAGCTCACTGCAA TTGAGACAGAGTCTCACTCCATCACCCAGGCTGGAGTGTAATGGTGCCACCTCAGCTCACTGCAA T C ZNF561 Ensembl:ENSG00000171469 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs888244479 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127779,RMVar_hsa_circ_125881,RMVar_hsa_circ_296937,RMVar_hsa_circ_192222,RMVar_hsa_circ_310289,RMVar_hsa_circ_296240,RMVar_hsa_circ_192223,RMVar_hsa_circ_192224 24203 RMVar_ID_24203 Human_SNP_ID_657963954 A-to-I Human chr19 - 9647261 9647253 9647262 CCTGGCCAACATGTTGAAACCCCGTCTTTACTAAAAATACAAAAATTAGCTGGGCACGGTATTGT CCTGGCCAACATGTTGAAACCCCGTCTTTAC_________AAAAATTAGCTGGGCACGGTATTGT TGTATTTTTA T ZNF562 Ensembl:ENSG00000171466 Protein coding 3'UTR GSE100210;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229 RNA-Seq:(High) rs780592055 Functional Loss DEL dbSNP153 32..40 33 - - - RMVar_hsa_circ_127779,RMVar_hsa_circ_192224,RMVar_hsa_circ_192227 24204 RMVar_ID_24204 Human_SNP_ID_657964291 A-to-I Human chr19 - 9648529 9648528 9648530 GGAGGTGGGGGTGGGCAGATCATTTGAGGTCAAGAGTTCGAGACCAGCCCAGCCAACATGGTGAA GGAGGTGGGGGTGGGCAGATCATTTGAGGTC__GAGTTCGAGACCAGCCCAGCCAACATGGTGAA CTT C ZNF562 Ensembl:ENSG00000171466 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1283565116 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_127779,RMVar_hsa_circ_192224,RMVar_hsa_circ_192227 24205 RMVar_ID_24205 Human_SNP_ID_657964969 A-to-I Human chr19 + 9650767 9650746 9650767 AGGTCAGATCTGACCAACATGGAGATCAGCCTAACCAACATGGAGAAACCCTGTCTCTACTAAAA AGGTCAGATCTG_____________________ACCAACATGGAGAAACCCTGTCTCTACTAAAA GACCAACATGGAGATCAGCCTA G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1255120193 Functional Loss DEL dbSNP153 13..33 33 - - - 24206 RMVar_ID_24206 Human_SNP_ID_657964994 A-to-I Human chr19 - 9650867 9650867 9650867 TCACCGCAACCTCCACCTCCTGAGTTCCAGTGATTCTCCTGCCTCACCCTCAGTAGCTGGGATTA TCACCGCAACCTCCACCTCCTGAGTTCCAGTGGTTCTCCTGCCTCACCCTCAGTAGCTGGGATTA T C ZNF562 Ensembl:ENSG00000171466 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1194654600 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26471949 RMVar_hsa_circ_127779,RMVar_hsa_circ_192224,RMVar_hsa_circ_192227,RMVar_hsa_circ_192229,RMVar_hsa_circ_125287,RMVar_hsa_circ_266760 24207 RMVar_ID_24207 Human_SNP_ID_657966528 A-to-I Human chr19 + 9655836 9655836 9655836 GCTCACTCAGCAACCTCGGCCTCTGGGTAAGCAATTGTCCTGCCTCAGCCGCCCGAGTAACTAGG GCTCACTCAGCAACCTCGGCCTCTGGGTAAGCGATTGTCCTGCCTCAGCCGCCCGAGTAACTAGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879064916 Functional Loss SNV dbSNP153 33..33 33 - - - 24208 RMVar_ID_24208 Human_SNP_ID_657968334 A-to-I Human chr19 - 9661539 9661539 9661539 CACCTGCCTTGGCCTCCCAAAGTGTTGGGATTACAGGCATGAGCCACCGTGCCTGACCAACCCCA CACCTGCCTTGGCCTCCCAAAGTGTTGGGATTGCAGGCATGAGCCACCGTGCCTGACCAACCCCA T C ZNF562 Ensembl:ENSG00000171466 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1228602500 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_192227 24209 RMVar_ID_24209 Human_SNP_ID_657968483 A-to-I Human chr19 - 9662034 9662034 9662034 TAATAGGCCAGGCATGGTGGCTCATGCTTATTATCCCAGCACTTTGGGAGGCCAAGGTGGGAGGA TAATAGGCCAGGCATGGTGGCTCATGCTTATTTTCCCAGCACTTTGGGAGGCCAAGGTGGGAGGA T A ZNF562 Ensembl:ENSG00000171466 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs914078092 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_192227 24210 RMVar_ID_24210 Human_SNP_ID_657968484 A-to-I Human chr19 - 9662037 9662037 9662037 AGGTAATAGGCCAGGCATGGTGGCTCATGCTTATTATCCCAGCACTTTGGGAGGCCAAGGTGGGA AGGTAATAGGCCAGGCATGGTGGCTCATGCTTCTTATCCCAGCACTTTGGGAGGCCAAGGTGGGA T G ZNF562 Ensembl:ENSG00000171466 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1204307405 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_192227 24211 RMVar_ID_24211 Human_SNP_ID_657969071 A-to-I Human chr19 - 9663888 9663888 9663888 AAAATAGCTGGGAATGGTGGCATGCACCTGTAATCCCAGCTATTTGGGAGGCTGTGGCAGGAGAA AAAATAGCTGGGAATGGTGGCATGCACCTGTAGTCCCAGCTATTTGGGAGGCTGTGGCAGGAGAA T C ZNF562 Ensembl:ENSG00000171466 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1473294059 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_192227 24212 RMVar_ID_24212 Human_SNP_ID_657970087 A-to-I Human chr19 - 9667750 9667750 9667750 TCTGCCCCCAGTCTCTAAAAAAAAAAAAAGTTAGCATTGTCACACATGCCTGTGGTTCTAGCTAC TCTGCCCCCAGTCTCTAAAAAAAAAAAAAGTTTGCATTGTCACACATGCCTGTGGTTCTAGCTAC T A ZNF562 Ensembl:ENSG00000171466 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1021162738 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17567916 RMVar_hsa_circ_192227 24213 RMVar_ID_24213 Human_SNP_ID_657970088 A-to-I Human chr19 - 9667750 9667750 9667750 TCTGCCCCCAGTCTCTAAAAAAAAAAAAAGTTAGCATTGTCACACATGCCTGTGGTTCTAGCTAC TCTGCCCCCAGTCTCTAAAAAAAAAAAAAGTTGGCATTGTCACACATGCCTGTGGTTCTAGCTAC T C ZNF562 Ensembl:ENSG00000171466 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1021162738 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17567916 RMVar_hsa_circ_192227 24214 RMVar_ID_24214 Human_SNP_ID_657970089 A-to-I Human chr19 - 9667750 9667750 9667750 TCTGCCCCCAGTCTCTAAAAAAAAAAAAAGTTAGCATTGTCACACATGCCTGTGGTTCTAGCTAC TCTGCCCCCAGTCTCTAAAAAAAAAAAAAGTTCGCATTGTCACACATGCCTGTGGTTCTAGCTAC T G ZNF562 Ensembl:ENSG00000171466 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1021162738 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17567916 RMVar_hsa_circ_192227 24215 RMVar_ID_24215 Human_SNP_ID_657971285 A-to-I Human chr19 - 9670914 9670914 9670914 CTCACTGCAACCTCTGCCTCCTCCCGGATTCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCT CTCACTGCAACCTCTGCCTCCTCCCGGATTCAGGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCT T C ZNF562 Ensembl:ENSG00000171466 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs772976770 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_192227 24216 RMVar_ID_24216 Human_SNP_ID_657971944 A-to-I Human chr19 - 9673249 9673249 9673249 GAAGGGGTTTTTATTTCTAACGCTGGGTCCCTACTTCTGTGTCTCTCCCCCGTGGGTTAGGGTCA GAAGGGGTTTTTATTTCTAACGCTGGGTCCCTGCTTCTGTGTCTCTCCCCCGTGGGTTAGGGTCA T C ZNF562 Ensembl:ENSG00000171466 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1412893330 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17567918 RMVar_hsa_circ_192227 24217 RMVar_ID_24217 Human_SNP_ID_657972215 A-to-I Human chr19 - 9674119 9674119 9674119 TGGAATTAGTTTAGCCTGTGGGGTCTAACCCTAGCCATCGGGGAAGGACAAAGCGGCAGGGGCCA TGGAATTAGTTTAGCCTGTGGGGTCTAACCCTTGCCATCGGGGAAGGACAAAGCGGCAGGGGCCA T A ZNF562 Ensembl:ENSG00000171466 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs550322223 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13541994 RMVar_hsa_circ_192227 24218 RMVar_ID_24218 Human_SNP_ID_657972216 A-to-I Human chr19 - 9674119 9674119 9674119 TGGAATTAGTTTAGCCTGTGGGGTCTAACCCTAGCCATCGGGGAAGGACAAAGCGGCAGGGGCCA TGGAATTAGTTTAGCCTGTGGGGTCTAACCCTGGCCATCGGGGAAGGACAAAGCGGCAGGGGCCA T C ZNF562 Ensembl:ENSG00000171466 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs550322223 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13541994 RMVar_hsa_circ_192227 24219 RMVar_ID_24219 Human_SNP_ID_657973198 A-to-I Human chr19 + 9676396 9676396 9676396 AAGATGATCCCCATCTCCTGACCTCATGATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTAC AAGATGATCCCCATCTCCTGACCTCATGATCCCCCCGCCTCGGCCTCCCAAAGTGCTGGGATTAC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs923025995 Functional Loss SNV dbSNP153 33..33 33 - - - 24220 RMVar_ID_24220 Human_SNP_ID_657974126 A-to-I Human chr19 + 9679201 9679201 9679201 AAAAATAGGCTCGGCTGGTGGCTCACGCCTGTAATCCCAGTACTTTGAGAGGCCGAGGTGGGTGA AAAAATAGGCTCGGCTGGTGGCTCACGCCTGTCATCCCAGTACTTTGAGAGGCCGAGGTGGGTGA A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202989821 Functional Loss SNV dbSNP153 33..33 33 - - - 24221 RMVar_ID_24221 Human_SNP_ID_657993586 A-to-I Human chr19 - 9734381 9734381 9734381 ATTTAGGCTGGGCACAGTGGCTCACACCTGTAATCCCAGCACTTTGGAAGGCCGAGGCGGGTGGC ATTTAGGCTGGGCACAGTGGCTCACACCTGTAGTCCCAGCACTTTGGAAGGCCGAGGCGGGTGGC T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1200281812 Functional Loss SNV dbSNP153 33..33 33 - - - 24222 RMVar_ID_24222 Human_SNP_ID_658003793 A-to-I Human chr19 - 9767163 9767163 9767163 GCAATGCACTACAGCCTGGGCAACAAGAGCAAAACACCGTCTAAATAAATAAATAAATAAATAAA GCAATGCACTACAGCCTGGGCAACAAGAGCAAGACACCGTCTAAATAAATAAATAAATAAATAAA T C ZNF846 Ensembl:ENSG00000196605 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1391020223 Functional Loss SNV dbSNP153 33..33 33 - - - 24223 RMVar_ID_24223 Human_SNP_ID_658015948 A-to-I Human chr19 - 9811578 9811578 9811578 GTCCCCTGCTCTGTTGAGAGCCCTGGGCCAGAAGTGCCCCAACCTGAAGCGCCTCTGCCTGCACG GTCCCCTGCTCTGTTGAGAGCCCTGGGCCAGACGTGCCCCAACCTGAAGCGCCTCTGCCTGCACG T G FBXL12 Ensembl:ENSG00000127452 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs369872231 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4556791,Human_RBP_ID_22069326,Human_RBP_ID_26471953 RMVar_hsa_circ_80216,RMVar_hsa_circ_107478,RMVar_hsa_circ_192241,RMVar_hsa_circ_192242 24224 RMVar_ID_24224 Human_SNP_ID_658016106 A-to-I Human chr19 - 9812107 9812107 9812107 CCTGGGCAACATAGCAAGACCTCATCTCTACTAAAAATCACAAAAATTAGCTGGGCATGTGTCAG CCTGGGCAACATAGCAAGACCTCATCTCTACTGAAAATCACAAAAATTAGCTGGGCATGTGTCAG T C FBXL12 Ensembl:ENSG00000127452 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs73014068 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2308,GWAS_ID_2309,GWAS_ID_2310,GWAS_ID_2311,GWAS_ID_2312,GWAS_ID_2313,GWAS_ID_2314,GWAS_ID_2315,GWAS_ID_2316,GWAS_ID_2317,GWAS_ID_2318,GWAS_ID_2319,GWAS_ID_2320,GWAS_ID_2321,GWAS_ID_2322 RMVar_hsa_circ_80216,RMVar_hsa_circ_107478,RMVar_hsa_circ_192241,RMVar_hsa_circ_192242 24225 RMVar_ID_24225 Human_SNP_ID_658016108 A-to-I Human chr19 - 9812110 9812110 9812110 CAGCCTGGGCAACATAGCAAGACCTCATCTCTACTAAAAATCACAAAAATTAGCTGGGCATGTGT CAGCCTGGGCAACATAGCAAGACCTCATCTCTGCTAAAAATCACAAAAATTAGCTGGGCATGTGT T C FBXL12 Ensembl:ENSG00000127452 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1213753107 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80216,RMVar_hsa_circ_107478,RMVar_hsa_circ_192241,RMVar_hsa_circ_192242 24226 RMVar_ID_24226 Human_SNP_ID_658016499 A-to-I Human chr19 - 9813578 9813562 9813578 AGAATTGCTTGAACCTGGGAGGTGGAGATTGCAGTGAGCCGAGATTGCGCTACTGCACTCCAGCC AGAATTGCTTGAACCTGGGAGGTGGAGATTGC________________GCTACTGCACTCCAGCC CGCAATCTCGGCTCACT C FBXL12 Ensembl:ENSG00000127452 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1232696227 Functional Loss DEL dbSNP153 33..48 33 - - - Human_RBP_ID_25440577 RMVar_hsa_circ_80216,RMVar_hsa_circ_107478,RMVar_hsa_circ_192241,RMVar_hsa_circ_192242 24227 RMVar_ID_24227 Human_SNP_ID_658016679 A-to-I Human chr19 - 9814338 9814338 9814338 ACTCGGCTAATTTTTTTTTGTATTTTAGTAGAAACGGGGTTTTGTCATGTTGGCCAGGATGGTCT ACTCGGCTAATTTTTTTTTGTATTTTAGTAGATACGGGGTTTTGTCATGTTGGCCAGGATGGTCT T A FBXL12 Ensembl:ENSG00000127452 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1387270686 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13542200,Human_RBP_ID_18742814 Human_Splice_Rec_1952542,Human_Splice_Rec_1952554 RMVar_hsa_circ_80216,RMVar_hsa_circ_107478,RMVar_hsa_circ_192241,RMVar_hsa_circ_192242 24228 RMVar_ID_24228 Human_SNP_ID_658016696 A-to-I Human chr19 - 9814388 9814388 9814388 CTCCTACCTCAGCCTCCTTAGTAGCTGGGACTACAGGCATGCACCACCACACTCGGCTAATTTTT CTCCTACCTCAGCCTCCTTAGTAGCTGGGACTTCAGGCATGCACCACCACACTCGGCTAATTTTT T A FBXL12 Ensembl:ENSG00000127452 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1047985581 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80216,RMVar_hsa_circ_107478,RMVar_hsa_circ_192241,RMVar_hsa_circ_192242 24229 RMVar_ID_24229 Human_SNP_ID_658016697 A-to-I Human chr19 - 9814398 9814398 9814398 TCAAGCGATTCTCCTACCTCAGCCTCCTTAGTAGCTGGGACTACAGGCATGCACCACCACACTCG TCAAGCGATTCTCCTACCTCAGCCTCCTTAGTGGCTGGGACTACAGGCATGCACCACCACACTCG T C FBXL12 Ensembl:ENSG00000127452 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1050277089 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80216,RMVar_hsa_circ_107478,RMVar_hsa_circ_192241,RMVar_hsa_circ_192242 24230 RMVar_ID_24230 Human_SNP_ID_658016702 A-to-I Human chr19 - 9814428 9814428 9814428 TCAGTTCACTGGAACCTCTGCCTCCCGTGTTCAAGCGATTCTCCTACCTCAGCCTCCTTAGTAGC TCAGTTCACTGGAACCTCTGCCTCCCGTGTTCGAGCGATTCTCCTACCTCAGCCTCCTTAGTAGC T C FBXL12 Ensembl:ENSG00000127452 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1019684768 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80216,RMVar_hsa_circ_107478,RMVar_hsa_circ_192241,RMVar_hsa_circ_192242 24231 RMVar_ID_24231 Human_SNP_ID_658016736 A-to-I Human chr19 - 9814575 9814575 9814575 CCCCTGCCTCAGCCTCCTGAGAAGCTGGGACTACAGGCACGTGCCACCACACTGAGCTAATTTTT CCCCTGCCTCAGCCTCCTGAGAAGCTGGGACTGCAGGCACGTGCCACCACACTGAGCTAATTTTT T C FBXL12 Ensembl:ENSG00000127452 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1399456630 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1952540 RMVar_hsa_circ_80216,RMVar_hsa_circ_107478,RMVar_hsa_circ_192241,RMVar_hsa_circ_192242 24232 RMVar_ID_24232 Human_SNP_ID_658019555 A-to-I Human chr19 - 9824384 9824384 9824384 GGGAGGCCAAGGCAGGCGGATTGTGTGAGTTCAGGAGTTGGAGACCAGCCTGGGCAACACGCTGA GGGAGGCCAAGGCAGGCGGATTGTGTGAGTTCGGGAGTTGGAGACCAGCCTGGGCAACACGCTGA T C FBXL12 Ensembl:ENSG00000127452 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1325056580 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23812905 24233 RMVar_ID_24233 Human_SNP_ID_658019566 A-to-I Human chr19 - 9824429 9824429 9824429 ATATAGGCCAGGTGTGGTGGCTCACACCTGTAATCCTGGCACTTTGGGAGGCCAAGGCAGGCGGA ATATAGGCCAGGTGTGGTGGCTCACACCTGTAGTCCTGGCACTTTGGGAGGCCAAGGCAGGCGGA T C FBXL12 Ensembl:ENSG00000127452 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1372316348 Functional Loss SNV dbSNP153 33..33 33 - - - 24234 RMVar_ID_24234 Human_SNP_ID_658019602 A-to-I Human chr19 - 9824572 9824572 9824572 CTGCCTCGGCCTCCCAAAGTGCTGGGATTACAAGTGTAAGCAACCACACCCAACCTCTCTTCTGT CTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTAAGCAACCACACCCAACCTCTCTTCTGT T C FBXL12 Ensembl:ENSG00000127452 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223163502 Functional Loss SNV dbSNP153 33..33 33 - - - 24235 RMVar_ID_24235 Human_SNP_ID_658019636 A-to-I Human chr19 - 9824703 9824703 9824703 GCAACAAGAGAGAAACTCCCAGGATTACAGGCATGCACCACCATGCCTAGCTAATTTTGTATTTT GCAACAAGAGAGAAACTCCCAGGATTACAGGCGTGCACCACCATGCCTAGCTAATTTTGTATTTT T C FBXL12 Ensembl:ENSG00000127452 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1034951236 Functional Loss SNV dbSNP153 33..33 33 - - - 24236 RMVar_ID_24236 Human_SNP_ID_658020066 A-to-I Human chr19 - 9826530 9826530 9826530 CGCCGTTGTCCTGCCTCAGCCGCCTCCCGAGTAACAGGGACTACAGGCGCCCCCCACCACCCTCG CGCCGTTGTCCTGCCTCAGCCGCCTCCCGAGTTACAGGGACTACAGGCGCCCCCCACCACCCTCG T A FBXL12 Ensembl:ENSG00000127452 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs895165195 Functional Loss SNV dbSNP153 33..33 33 - - - 24237 RMVar_ID_24237 Human_SNP_ID_658020067 A-to-I Human chr19 - 9826530 9826530 9826530 CGCCGTTGTCCTGCCTCAGCCGCCTCCCGAGTAACAGGGACTACAGGCGCCCCCCACCACCCTCG CGCCGTTGTCCTGCCTCAGCCGCCTCCCGAGTGACAGGGACTACAGGCGCCCCCCACCACCCTCG T C FBXL12 Ensembl:ENSG00000127452 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs895165195 Functional Loss SNV dbSNP153 33..33 33 - - - 24238 RMVar_ID_24238 Human_SNP_ID_658020217 A-to-I Human chr19 - 9827100 9827100 9827100 TAGTCTCGCTCTGTTGCACAGGCTGGAGTGCAATGGCGCGGTGCCGGCTCACCGCAACCTCCGCC TAGTCTCGCTCTGTTGCACAGGCTGGAGTGCAGTGGCGCGGTGCCGGCTCACCGCAACCTCCGCC T C FBXL12 Ensembl:ENSG00000127452 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1424440738 Functional Loss SNV dbSNP153 33..33 33 - - - 24239 RMVar_ID_24239 Human_SNP_ID_658023842 A-to-I Human chr19 + 9839893 9839893 9839893 ATGGTGGTGCACGCCTGTAGTGTCAGCTACTTAGAAGACTGAGGTGGGAGGATCCTTTGAGCCCA ATGGTGGTGCACGCCTGTAGTGTCAGCTACTTCGAAGACTGAGGTGGGAGGATCCTTTGAGCCCA A C PIN1 Ensembl:ENSG00000127445 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1347331269 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73570,RMVar_hsa_circ_108096,RMVar_hsa_circ_192252 24240 RMVar_ID_24240 Human_SNP_ID_658028000 A-to-I Human chr19 - 9855076 9855076 9855076 GGTTAGTGGTCACTGGACAGCCATTGAGTGATAAGACGTCACTTGAATTCACTGCCCATGGTTAA GGTTAGTGGTCACTGGACAGCCATTGAGTGATGAGACGTCACTTGAATTCACTGCCCATGGTTAA T C OLFM2 Ensembl:ENSG00000105088 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1467901240 Functional Loss SNV dbSNP153 33..33 33 - - - 24241 RMVar_ID_24241 Human_SNP_ID_658036377 A-to-I Human chr19 - 9888335 9888335 9888335 ATTTTTAGTAGAGACGGGGGTTTCACCATGTTAGCCAGGCTGGTCTCGAACTCCCGACCTCAAAT ATTTTTAGTAGAGACGGGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCCGACCTCAAAT T C OLFM2 Ensembl:ENSG00000105088 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs185687426 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97001,RMVar_hsa_circ_192254 24242 RMVar_ID_24242 Human_SNP_ID_658036379 A-to-I Human chr19 - 9888340 9888340 9888340 TTTGTATTTTTAGTAGAGACGGGGGTTTCACCATGTTAGCCAGGCTGGTCTCGAACTCCCGACCT TTTGTATTTTTAGTAGAGACGGGGGTTTCACCGTGTTAGCCAGGCTGGTCTCGAACTCCCGACCT T C OLFM2 Ensembl:ENSG00000105088 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1212436785 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97001,RMVar_hsa_circ_192254 24243 RMVar_ID_24243 Human_SNP_ID_658036380 A-to-I Human chr19 - 9888343 9888343 9888343 ATTTTTGTATTTTTAGTAGAGACGGGGGTTTCACCATGTTAGCCAGGCTGGTCTCGAACTCCCGA ATTTTTGTATTTTTAGTAGAGACGGGGGTTTCGCCATGTTAGCCAGGCTGGTCTCGAACTCCCGA T C OLFM2 Ensembl:ENSG00000105088 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1484374975 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97001,RMVar_hsa_circ_192254 24244 RMVar_ID_24244 Human_SNP_ID_658036428 A-to-I Human chr19 - 9888461 9888461 9888461 GGAGTGTAGTCGCATGATCTCAGCTCACCGCAACCTCCGCCCCCCAGGCTCAAGCGATTCTCCTG GGAGTGTAGTCGCATGATCTCAGCTCACCGCAGCCTCCGCCCCCCAGGCTCAAGCGATTCTCCTG T C OLFM2 Ensembl:ENSG00000105088 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1354507648 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97001,RMVar_hsa_circ_192254 24245 RMVar_ID_24245 Human_SNP_ID_658086652 A-to-I Human chr19 + 10061175 10061175 10061175 TTTTTGTCATCCAGGCTGGACTGCAATGGCACAATCTCAGCTCACTGCAACCTCCACCTCCCAGG TTTTTGTCATCCAGGCTGGACTGCAATGGCACCATCTCAGCTCACTGCAACCTCCACCTCCCAGG A C C3P1 Ensembl:ENSG00000167798 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1432227635 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69951,RMVar_hsa_circ_369064 24246 RMVar_ID_24246 Human_SNP_ID_658086654 A-to-I Human chr19 + 10061181 10061181 10061181 TCATCCAGGCTGGACTGCAATGGCACAATCTCAGCTCACTGCAACCTCCACCTCCCAGGTTCAAG TCATCCAGGCTGGACTGCAATGGCACAATCTCGGCTCACTGCAACCTCCACCTCCCAGGTTCAAG A G C3P1 Ensembl:ENSG00000167798 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1421927574 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69951,RMVar_hsa_circ_369064 24247 RMVar_ID_24247 Human_SNP_ID_658086657 A-to-I Human chr19 + 10061198 10061198 10061198 CAATGGCACAATCTCAGCTCACTGCAACCTCCACCTCCCAGGTTCAAGTGATTCTCCTGCCTCAG CAATGGCACAATCTCAGCTCACTGCAACCTCCGCCTCCCAGGTTCAAGTGATTCTCCTGCCTCAG A G C3P1 Ensembl:ENSG00000167798 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1340495538 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69951,RMVar_hsa_circ_369064 24248 RMVar_ID_24248 Human_SNP_ID_658096966 A-to-I Human chr19 - 10096911 10096911 10096911 TTTTTTTTTTTTGTAGAGACAGGGGTCTCCCCATGTTGCCCAGGCTGGTCTCGAACTCCTGGTCT TTTTTTTTTTTTGTAGAGACAGGGGTCTCCCCGTGTTGCCCAGGCTGGTCTCGAACTCCTGGTCT T C ANGPTL6 Ensembl:ENSG00000130812 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1351242820 Functional Loss SNV dbSNP153 33..33 33 - - - 24249 RMVar_ID_24249 Human_SNP_ID_658096967 A-to-I Human chr19 - 10096911 10096911 10096911 TTTTTTTTTTTTGTAGAGACAGGGGTCTCCCCATGTTGCCCAGGCTGGTCTCGAACTCCTGGTCT TTTTTTTTTTTTGTAGAGACAGGGGTCTCCCCCTGTTGCCCAGGCTGGTCTCGAACTCCTGGTCT T G ANGPTL6 Ensembl:ENSG00000130812 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1351242820 Functional Loss SNV dbSNP153 33..33 33 - - - 24250 RMVar_ID_24250 Human_SNP_ID_658096976 A-to-I Human chr19 - 10096929 10096929 10096929 ACGTCTGTCTAATTTTTTTTTTTTTTTTTTGTAGAGACAGGGGTCTCCCCATGTTGCCCAGGCTG ACGTCTGTCTAATTTTTTTTTTTTTTTTTTGTTGAGACAGGGGTCTCCCCATGTTGCCCAGGCTG T A ANGPTL6 Ensembl:ENSG00000130812 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1186031877 Functional Loss SNV dbSNP153 33..33 33 - - - 24251 RMVar_ID_24251 Human_SNP_ID_658096977 A-to-I Human chr19 - 10096929 10096929 10096929 ACGTCTGTCTAATTTTTTTTTTTTTTTTTTGTAGAGACAGGGGTCTCCCCATGTTGCCCAGGCTG ACGTCTGTCTAATTTTTTTTTTTTTTTTTTGTGGAGACAGGGGTCTCCCCATGTTGCCCAGGCTG T C ANGPTL6 Ensembl:ENSG00000130812 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1186031877 Functional Loss SNV dbSNP153 33..33 33 - - - 24252 RMVar_ID_24252 Human_SNP_ID_658098138 A-to-I Human chr19 - 10101190 10101190 10101190 TTTTATTTTTTTTTGAGACAGAGTCTCGCTCTATTGCCCAGGCTGGAGTGCAGTGGTGCAATCAT TTTTATTTTTTTTTGAGACAGAGTCTCGCTCTGTTGCCCAGGCTGGAGTGCAGTGGTGCAATCAT T C ANGPTL6 Ensembl:ENSG00000130812 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs980034412 Functional Loss SNV dbSNP153 33..33 33 - - - 24253 RMVar_ID_24253 Human_SNP_ID_658101083 A-to-I Human chr19 + 10109101 10109101 10109101 CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGTGCCCGCCACCACACCCCGGCTAATTTT CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTGCAGGTGCCCGCCACCACACCCCGGCTAATTTT A G PPAN,PPAN-P2RY11 Ensembl:ENSG00000130810,Ensembl:ENSG00000243207 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1287947847 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82075,RMVar_hsa_circ_77059,RMVar_hsa_circ_192260,RMVar_hsa_circ_192261 24254 RMVar_ID_24254 Human_SNP_ID_658101176 A-to-I Human chr19 + 10109319 10109319 10109319 TCTCCGTACGTTGGTCTTGAACTCCTGGGCACAAGCAATCCTGCAGCCTCCGCTTCCCGAGTAGC TCTCCGTACGTTGGTCTTGAACTCCTGGGCACGAGCAATCCTGCAGCCTCCGCTTCCCGAGTAGC A G PPAN,PPAN-P2RY11 Ensembl:ENSG00000130810,Ensembl:ENSG00000243207 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs534523515 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13355036 RMVar_hsa_circ_82075,RMVar_hsa_circ_77059,RMVar_hsa_circ_192260,RMVar_hsa_circ_192261 24255 RMVar_ID_24255 Human_SNP_ID_658104172 A-to-I Human chr19 - 10115065 10115065 10115065 TACTCGGTCCGGGACCCTTGGCGACAGAAGACAGCCTCCGAGAGCGCGGGCTCCAAGGGCAATAA TACTCGGTCCGGGACCCTTGGCGACAGAAGACGGCCTCCGAGAGCGCGGGCTCCAAGGGCAATAA T C EIF3G Ensembl:ENSG00000130811 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs775096789 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_511913,Human_RBP_ID_771699,Human_RBP_ID_1553168,Human_RBP_ID_4497513,Human_RBP_ID_5585210,Human_RBP_ID_8475906,Human_RBP_ID_9328567,Human_RBP_ID_13355173,Human_RBP_ID_17655924,Human_RBP_ID_18191930,Human_RBP_ID_18721066,Human_RBP_ID_18994248,Human_RBP_ID_22966140,Human_RBP_ID_24552685,Human_RBP_ID_26474430,Human_RBP_ID_26981184 Human_Splice_Rec_1953286,Human_Splice_Rec_1953294,Human_Splice_Rec_1953300 Human_miRNA_ID_1395757,Human_miRNA_ID_2716249,Human_miRNA_ID_3052234 RMVar_hsa_circ_102942,RMVar_hsa_circ_124534,RMVar_hsa_circ_192266,RMVar_hsa_circ_87997,RMVar_hsa_circ_192267,RMVar_hsa_circ_192265 24256 RMVar_ID_24256 Human_SNP_ID_658113209 A-to-I Human chr19 - 10144356 10144356 10144356 TCACACAGGCTGGAGTGCAGTGGCACAATCTCAGCTCACTGCAACCTCTGCCTCCTGGGTTCAAG TCACACAGGCTGGAGTGCAGTGGCACAATCTCGGCTCACTGCAACCTCTGCCTCCTGGGTTCAAG T C DNMT1 Ensembl:ENSG00000130816 Protein coding exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1202549149 Functional Loss SNV dbSNP153 33..33 33 - - - 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_33091,RMVar_hsa_circ_123671,RMVar_hsa_circ_192282,RMVar_hsa_circ_118627,RMVar_hsa_circ_323366,RMVar_hsa_circ_265839,RMVar_hsa_circ_102895,RMVar_hsa_circ_20258,RMVar_hsa_circ_192287,RMVar_hsa_circ_90160,RMVar_hsa_circ_192285,RMVar_hsa_circ_192286,RMVar_hsa_circ_307539,RMVar_hsa_circ_348475,RMVar_hsa_circ_192288 24257 RMVar_ID_24257 Human_SNP_ID_658113211 A-to-I Human chr19 - 10144361 10144361 10144361 CTCTGTCACACAGGCTGGAGTGCAGTGGCACAATCTCAGCTCACTGCAACCTCTGCCTCCTGGGT CTCTGTCACACAGGCTGGAGTGCAGTGGCACAGTCTCAGCTCACTGCAACCTCTGCCTCCTGGGT T C DNMT1 Ensembl:ENSG00000130816 Protein coding exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs541211091 Functional Loss SNV dbSNP153 33..33 33 - - - 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_33091,RMVar_hsa_circ_123671,RMVar_hsa_circ_192282,RMVar_hsa_circ_118627,RMVar_hsa_circ_323366,RMVar_hsa_circ_265839,RMVar_hsa_circ_102895,RMVar_hsa_circ_20258,RMVar_hsa_circ_192287,RMVar_hsa_circ_90160,RMVar_hsa_circ_192285,RMVar_hsa_circ_192286,RMVar_hsa_circ_307539,RMVar_hsa_circ_348475,RMVar_hsa_circ_192288 24258 RMVar_ID_24258 Human_SNP_ID_658117770 A-to-I Human chr19 - 10160801 10160801 10160801 CTTACTGCAACCTCTACGTCTCGGGTTCAAGCAATTCTTCTGCCTCAGCCTTCTGAGTATCTGAG CTTACTGCAACCTCTACGTCTCGGGTTCAAGCTATTCTTCTGCCTCAGCCTTCTGAGTATCTGAG T A DNMT1 Ensembl:ENSG00000130816 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1288644977 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13356254 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_105547,RMVar_hsa_circ_20992,RMVar_hsa_circ_71818,RMVar_hsa_circ_294589,RMVar_hsa_circ_68450,RMVar_hsa_circ_192293,RMVar_hsa_circ_192294,RMVar_hsa_circ_84273,RMVar_hsa_circ_26817,RMVar_hsa_circ_316491,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_370794,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_192306,RMVar_hsa_circ_53249,RMVar_hsa_circ_47164 24259 RMVar_ID_24259 Human_SNP_ID_658118154 A-to-I Human chr19 - 10162220 10162220 10162220 GCATGAGAATTGCTTGAACCCAGGAGGCGGAGATTGCTGTGAGCTGAGATCGTGCCACTGTACTC GCATGAGAATTGCTTGAACCCAGGAGGCGGAGGTTGCTGTGAGCTGAGATCGTGCCACTGTACTC T C DNMT1 Ensembl:ENSG00000130816 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7253898 Functional Loss SNV dbSNP153 33..33 33 - - - 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_105547,RMVar_hsa_circ_20992,RMVar_hsa_circ_71818,RMVar_hsa_circ_294589,RMVar_hsa_circ_68450,RMVar_hsa_circ_192293,RMVar_hsa_circ_192294,RMVar_hsa_circ_84273,RMVar_hsa_circ_26817,RMVar_hsa_circ_316491,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_370794,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_192306,RMVar_hsa_circ_53249,RMVar_hsa_circ_47164 24260 RMVar_ID_24260 Human_SNP_ID_658118766 A-to-I Human chr19 - 10164325 10164325 10164325 CAGCCTGACCAACATGGTGAAACCCCAGCTCTACTAAAAATACAGAATTAGCTGGGTGTGGTGGC CAGCCTGACCAACATGGTGAAACCCCAGCTCTGCTAAAAATACAGAATTAGCTGGGTGTGGTGGC T C DNMT1 Ensembl:ENSG00000130816 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs994691368 Functional Loss SNV dbSNP153 33..33 33 - - - 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_192316,RMVar_hsa_circ_284314 24261 RMVar_ID_24261 Human_SNP_ID_658118789 A-to-I Human chr19 - 10164415 10164415 10164415 TTGTAAGCCAGGCGCGGTGTCTCACGCCTATAATCCCAGCATTTTGGGACACTGAGGTGGGCGGA TTGTAAGCCAGGCGCGGTGTCTCACGCCTATAGTCCCAGCATTTTGGGACACTGAGGTGGGCGGA T C DNMT1 Ensembl:ENSG00000130816 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs924210907 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13356368,Human_RBP_ID_17567922,Human_RBP_ID_22808851,Human_RBP_ID_22966241 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_192316,RMVar_hsa_circ_284314 24262 RMVar_ID_24262 Human_SNP_ID_658118790 A-to-I Human chr19 - 10164418 10164418 10164418 TTTTTGTAAGCCAGGCGCGGTGTCTCACGCCTATAATCCCAGCATTTTGGGACACTGAGGTGGGC TTTTTGTAAGCCAGGCGCGGTGTCTCACGCCTGTAATCCCAGCATTTTGGGACACTGAGGTGGGC T C DNMT1 Ensembl:ENSG00000130816 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs148665266 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13356369,Human_RBP_ID_17567922,Human_RBP_ID_22808851,Human_RBP_ID_22966241 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_192316,RMVar_hsa_circ_284314 24263 RMVar_ID_24263 Human_SNP_ID_658119038 A-to-I Human chr19 - 10165143 10165142 10165143 CCTCAGCCTCCCAAGTAGCTGGGACTATAGGCAGGCACCACCATGTCCAGCTAATTTTTTTTTTT CCTCAGCCTCCCAAGTAGCTGGGACTATAGGC_GGCACCACCATGTCCAGCTAATTTTTTTTTTT CT C DNMT1 Ensembl:ENSG00000130816 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1555693163 Functional Loss DEL dbSNP153 33..33 33 - - - 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_192316,RMVar_hsa_circ_284314 24264 RMVar_ID_24264 Human_SNP_ID_658119132 A-to-I Human chr19 - 10165531 10165531 10165531 AAAATTAGCCGGGCATGGTGGCATGTGCCTCTAATCCCAGCTACTTGGGAGGCTGAGGTAGGAGA AAAATTAGCCGGGCATGGTGGCATGTGCCTCTCATCCCAGCTACTTGGGAGGCTGAGGTAGGAGA T G DNMT1 Ensembl:ENSG00000130816 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1004760258 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25380456 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_192316,RMVar_hsa_circ_284314 24265 RMVar_ID_24265 Human_SNP_ID_658119641 A-to-I Human chr19 - 10167360 10167360 10167360 AAACCCCGTCTCTAATAAAAATACAAAAAATTAGCTGGGTGTGGTGGTGCATGCCTGTGGTCCCA AAACCCCGTCTCTAATAAAAATACAAAAAATTCGCTGGGTGTGGTGGTGCATGCCTGTGGTCCCA T G DNMT1 Ensembl:ENSG00000130816 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1422722450 Functional Loss SNV dbSNP153 33..33 33 - - - 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_267045,RMVar_hsa_circ_192316,RMVar_hsa_circ_284314,RMVar_hsa_circ_327144,RMVar_hsa_circ_363399,RMVar_hsa_circ_60933 24266 RMVar_ID_24266 Human_SNP_ID_658119650 A-to-I Human chr19 - 10167398 10167398 10167398 GAGGTCAGGAGTTCAAGATCAGCCTGGCCAACATGGTGAAACCCCGTCTCTAATAAAAATACAAA GAGGTCAGGAGTTCAAGATCAGCCTGGCCAACGTGGTGAAACCCCGTCTCTAATAAAAATACAAA T C DNMT1 Ensembl:ENSG00000130816 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs545078817 Functional Loss SNV dbSNP153 33..33 33 - - - 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_267045,RMVar_hsa_circ_192316,RMVar_hsa_circ_284314,RMVar_hsa_circ_327144,RMVar_hsa_circ_363399,RMVar_hsa_circ_60933 24267 RMVar_ID_24267 Human_SNP_ID_658119773 A-to-I Human chr19 - 10167966 10167964 10167966 GGCCTGTACCACCATGCCCAACTAATTTTCGTATTTTTAGTAGAGACAGGGTTTCACCATATTGG GGCCTGTACCACCATGCCCAACTAATTTTCGT__TTTTAGTAGAGACAGGGTTTCACCATATTGG AAT A DNMT1 Ensembl:ENSG00000130816 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1381177424 Functional Loss DEL dbSNP153 33..34 33 - - - 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_267045,RMVar_hsa_circ_192316,RMVar_hsa_circ_284314,RMVar_hsa_circ_327144,RMVar_hsa_circ_363399,RMVar_hsa_circ_60933 24268 RMVar_ID_24268 Human_SNP_ID_658120191 A-to-I Human chr19 - 10169549 10169549 10169549 TATTTATTTACTTATTTATTTTTTGAGACGGAATCTCGCTCTTGTCGCCCAGGCTGGAGTGCAGT TATTTATTTACTTATTTATTTTTTGAGACGGAGTCTCGCTCTTGTCGCCCAGGCTGGAGTGCAGT T C DNMT1 Ensembl:ENSG00000130816 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1353009116 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13356532 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_378899,RMVar_hsa_circ_323045,RMVar_hsa_circ_61383,RMVar_hsa_circ_192310,RMVar_hsa_circ_364236,RMVar_hsa_circ_59709,RMVar_hsa_circ_303974,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_268592,RMVar_hsa_circ_192317 24269 RMVar_ID_24269 Human_SNP_ID_658120212 A-to-I Human chr19 - 10169644 10169644 10169644 CTCCTGCCTCAGCCTCCCGAGTAACTGGGACTACAGGCACCTGCTACCACGCCAGGCTAATTTTT CTCCTGCCTCAGCCTCCCGAGTAACTGGGACTGCAGGCACCTGCTACCACGCCAGGCTAATTTTT T C DNMT1 Ensembl:ENSG00000130816 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1422363956 Functional Loss SNV dbSNP153 33..33 33 - - - 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_378899,RMVar_hsa_circ_323045,RMVar_hsa_circ_61383,RMVar_hsa_circ_192310,RMVar_hsa_circ_364236,RMVar_hsa_circ_59709,RMVar_hsa_circ_303974,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_268592,RMVar_hsa_circ_192317 24270 RMVar_ID_24270 Human_SNP_ID_658122982 A-to-I Human chr19 - 10179755 10179755 10179755 GAACTCCTGACCTCAAGTGGTCCTCCCGCCTTAGCTTCCCAAAGTGCTGGGATTACAGGTGTGAG GAACTCCTGACCTCAAGTGGTCCTCCCGCCTTTGCTTCCCAAAGTGCTGGGATTACAGGTGTGAG T A DNMT1 Ensembl:ENSG00000130816 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs988850027 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13356928,Human_RBP_ID_25380715 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_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 24271 RMVar_ID_24271 Human_SNP_ID_658124149 A-to-I Human chr19 - 10182925 10182925 10182925 ATGGTGACTCATGCCTGTAATCCTAGCACTTCAGGAGACTGAGGCAGGCGGATCACTTGAGGTCA ATGGTGACTCATGCCTGTAATCCTAGCACTTCGGGAGACTGAGGCAGGCGGATCACTTGAGGTCA T C DNMT1 Ensembl:ENSG00000130816 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1223209970 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17568382,Human_RBP_ID_25380775 RMVar_hsa_circ_103673,RMVar_hsa_circ_192275,RMVar_hsa_circ_24852,RMVar_hsa_circ_192311 24272 RMVar_ID_24272 Human_SNP_ID_658124158 A-to-I Human chr19 - 10182961 10182961 10182961 TATATATATACGTGTATATATATATGCATGCCAGACATGGTGACTCATGCCTGTAATCCTAGCAC TATATATATACGTGTATATATATATGCATGCCGGACATGGTGACTCATGCCTGTAATCCTAGCAC T C DNMT1 Ensembl:ENSG00000130816 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1000008042 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17568382 RMVar_hsa_circ_103673,RMVar_hsa_circ_192275,RMVar_hsa_circ_24852,RMVar_hsa_circ_192311 24273 RMVar_ID_24273 Human_SNP_ID_658124409 A-to-I Human chr19 - 10183460 10183460 10183460 TCGCCTTGGCCTCCCAAAGTGCTGGGATTATAAGCGTGAGCCACCATGCCTGGTCTCTGGTACCT TCGCCTTGGCCTCCCAAAGTGCTGGGATTATATGCGTGAGCCACCATGCCTGGTCTCTGGTACCT T A DNMT1 Ensembl:ENSG00000130816 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1280471449 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103673,RMVar_hsa_circ_192275,RMVar_hsa_circ_24852,RMVar_hsa_circ_192311 24274 RMVar_ID_24274 Human_SNP_ID_658124410 A-to-I Human chr19 - 10183463 10183463 10183463 CGCTCGCCTTGGCCTCCCAAAGTGCTGGGATTATAAGCGTGAGCCACCATGCCTGGTCTCTGGTA CGCTCGCCTTGGCCTCCCAAAGTGCTGGGATTGTAAGCGTGAGCCACCATGCCTGGTCTCTGGTA T C DNMT1 Ensembl:ENSG00000130816 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1370271557 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23173376 RMVar_hsa_circ_103673,RMVar_hsa_circ_192275,RMVar_hsa_circ_24852,RMVar_hsa_circ_192311 24275 RMVar_ID_24275 Human_SNP_ID_658124423 A-to-I Human chr19 - 10183502 10183502 10183502 GTTTCCCAGGCTGGTCTGAACGCCTGGGCTCAAGTGATCCGCTCGCCTTGGCCTCCCAAAGTGCT GTTTCCCAGGCTGGTCTGAACGCCTGGGCTCACGTGATCCGCTCGCCTTGGCCTCCCAAAGTGCT T G DNMT1 Ensembl:ENSG00000130816 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1469153539 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13357024 RMVar_hsa_circ_103673,RMVar_hsa_circ_192275,RMVar_hsa_circ_24852,RMVar_hsa_circ_192311 24276 RMVar_ID_24276 Human_SNP_ID_658124430 A-to-I Human chr19 - 10183536 10183536 10183536 TTTTTGTATTTTTGTAGAGATGGAGTTTCGCCATGTTTCCCAGGCTGGTCTGAACGCCTGGGCTC TTTTTGTATTTTTGTAGAGATGGAGTTTCGCCTTGTTTCCCAGGCTGGTCTGAACGCCTGGGCTC T A DNMT1 Ensembl:ENSG00000130816 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1314363546 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13357026 RMVar_hsa_circ_103673,RMVar_hsa_circ_192275,RMVar_hsa_circ_24852,RMVar_hsa_circ_192311 24277 RMVar_ID_24277 Human_SNP_ID_658124487 A-to-I Human chr19 - 10183844 10183844 10183844 TGAGACAGAGTTTCACTCTTGTTGCCCAGGCTAGAGTGCAATGGTGTGACCAGCTCACTGCAACC TGAGACAGAGTTTCACTCTTGTTGCCCAGGCTGGAGTGCAATGGTGTGACCAGCTCACTGCAACC T C DNMT1 Ensembl:ENSG00000130816 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs191139097 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103673,RMVar_hsa_circ_192275,RMVar_hsa_circ_24852,RMVar_hsa_circ_192311 24278 RMVar_ID_24278 Human_SNP_ID_658143782 A-to-I Human chr19 + 10253676 10253676 10253676 AGCCGGACGTCTTAGTGCAAGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCATGAGAATCGCT AGCCGGACGTCTTAGTGCAAGCCTGTAGTCCCGGCTACTCAGGAGGCTGAGGCATGAGAATCGCT A G MRPL4 Ensembl:ENSG00000105364 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs561991805 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116491,RMVar_hsa_circ_98538,RMVar_hsa_circ_192329,RMVar_hsa_circ_192330 24279 RMVar_ID_24279 Human_SNP_ID_658143784 A-to-I Human chr19 + 10253684 10253684 10253684 GTCTTAGTGCAAGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCATGAGAATCGCTTGCACCTG GTCTTAGTGCAAGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCATGAGAATCGCTTGCACCTG A G MRPL4 Ensembl:ENSG00000105364 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1173798696 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116491,RMVar_hsa_circ_98538,RMVar_hsa_circ_192329,RMVar_hsa_circ_192330 24280 RMVar_ID_24280 Human_SNP_ID_658143909 A-to-I Human chr19 + 10254152 10254152 10254152 CTAATTCTCATGCCTCAGCCTCCCGAGTAGCCAGAATGACAGACATGTACCACCGTGCCCAGCTA CTAATTCTCATGCCTCAGCCTCCCGAGTAGCCGGAATGACAGACATGTACCACCGTGCCCAGCTA A G MRPL4 Ensembl:ENSG00000105364 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1046448873 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116491,RMVar_hsa_circ_98538,RMVar_hsa_circ_192329,RMVar_hsa_circ_192330 24281 RMVar_ID_24281 Human_SNP_ID_658149407 A-to-I Human chr19 + 10272743 10272743 10272743 ATGTGCCATCACACCCGGCTAATCACTGTGTTAGCCAGGATGGTCTCGATTTCCTGACCTCATGA ATGTGCCATCACACCCGGCTAATCACTGTGTTGGCCAGGATGGTCTCGATTTCCTGACCTCATGA A G ICAM1 Ensembl:ENSG00000090339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs780512191 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86287,RMVar_hsa_circ_192334 24282 RMVar_ID_24282 Human_SNP_ID_658149831 A-to-I Human chr19 + 10274408 10274408 10274408 ACAATCTTGGCTCACTGTAACCTCCACCTCCCAGGTTCAAGTGATTCTTGTGCCTCAGCCTCCCA ACAATCTTGGCTCACTGTAACCTCCACCTCCCGGGTTCAAGTGATTCTTGTGCCTCAGCCTCCCA A G ICAM1 Ensembl:ENSG00000090339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1355607895 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86287,RMVar_hsa_circ_192334 24283 RMVar_ID_24283 Human_SNP_ID_658150158 A-to-I Human chr19 + 10275610 10275610 10275610 GCAAATTAAGCCAAGTGTGGTGGCTTGTACCTATAATCCCAACTACTCCAGAGGCTGAGGCAGAA GCAAATTAAGCCAAGTGTGGTGGCTTGTACCTGTAATCCCAACTACTCCAGAGGCTGAGGCAGAA A G ICAM1 Ensembl:ENSG00000090339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1431178958 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86287,RMVar_hsa_circ_111775,RMVar_hsa_circ_192334,RMVar_hsa_circ_192335 24284 RMVar_ID_24284 Human_SNP_ID_658150763 A-to-I Human chr19 + 10277543 10277543 10277543 TGGAGTTTTGCTGTGTCCCCAGCCTGGAGTGCAATGGTGTAATCTCAGCTCACTGCAACCTCTCC TGGAGTTTTGCTGTGTCCCCAGCCTGGAGTGCGATGGTGTAATCTCAGCTCACTGCAACCTCTCC A G ICAM1 Ensembl:ENSG00000090339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs574479404 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86287,RMVar_hsa_circ_111775,RMVar_hsa_circ_192334,RMVar_hsa_circ_192335 24285 RMVar_ID_24285 Human_SNP_ID_658151197 A-to-I Human chr19 + 10279362 10279362 10279362 GCCCAGGAGTTCGAGACCAGCCTGGGCAACATAGCGAGACCCTGTCTCTAAGAAAAAATAAAAAA GCCCAGGAGTTCGAGACCAGCCTGGGCAACATGGCGAGACCCTGTCTCTAAGAAAAAATAAAAAA A G ICAM1 Ensembl:ENSG00000090339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs887834368 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86287,RMVar_hsa_circ_111775,RMVar_hsa_circ_192334,RMVar_hsa_circ_192335 24286 RMVar_ID_24286 Human_SNP_ID_658151910 A-to-I Human chr19 + 10281799 10281799 10281799 TCACTCAGTCTAGAGTACAGTGGCGCGATCTCAGTTCACTGCAATCTCTGCCTCCTGGGCTGAAG TCACTCAGTCTAGAGTACAGTGGCGCGATCTCTGTTCACTGCAATCTCTGCCTCCTGGGCTGAAG A T ICAM1 Ensembl:ENSG00000090339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs958364512 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86287,RMVar_hsa_circ_111775,RMVar_hsa_circ_192334,RMVar_hsa_circ_192335 24287 RMVar_ID_24287 Human_SNP_ID_658151930 A-to-I Human chr19 + 10281880 10281880 10281880 AGTAAACCTCAGCCTCTCAAGTAGCTGGGACTACAGGCACACAACACCACGCCTGGCTAATTTTT AGTAAACCTCAGCCTCTCAAGTAGCTGGGACTGCAGGCACACAACACCACGCCTGGCTAATTTTT A G ICAM1 Ensembl:ENSG00000090339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs958347406 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86287,RMVar_hsa_circ_111775,RMVar_hsa_circ_192334,RMVar_hsa_circ_192335 24288 RMVar_ID_24288 Human_SNP_ID_658152224 A-to-I Human chr19 + 10282968 10282968 10282968 CCAGGAGGCAGAGGTTGCAGTGAGCCAAGATCATGCCATCACCCTCCAGCCTGGGCGACAGAAGG CCAGGAGGCAGAGGTTGCAGTGAGCCAAGATCTTGCCATCACCCTCCAGCCTGGGCGACAGAAGG A T ICAM1 Ensembl:ENSG00000090339 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs990029272 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86287,RMVar_hsa_circ_111775,RMVar_hsa_circ_192334,RMVar_hsa_circ_192335 24289 RMVar_ID_24289 Human_SNP_ID_658165607 A-to-I Human chr19 - 10324817 10324817 10324817 CCGAGGAGCCCACCTTTAATGTTAGGTGACCCAGCTGAATGGAGGGTGGGCTTGACAGTGAAGCA CCGAGGAGCCCACCTTTAATGTTAGGTGACCCGGCTGAATGGAGGGTGGGCTTGACAGTGAAGCA T C RAVER1 Ensembl:ENSG00000161847 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs281423 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17567543 GWAS_ID_2323,GWAS_ID_2324,GWAS_ID_2325,GWAS_ID_2326,GWAS_ID_2327,GWAS_ID_2328,GWAS_ID_2329 RMVar_hsa_circ_38589,RMVar_hsa_circ_51169 24290 RMVar_ID_24290 Human_SNP_ID_658165832 A-to-I Human chr19 - 10325679 10325679 10325679 CCTCCCATGTAGCTGGGGAACTACAGGAATGCATCACCATGCCCAGCTGATTTTTAAAATTTTAT CCTCCCATGTAGCTGGGGAACTACAGGAATGCGTCACCATGCCCAGCTGATTTTTAAAATTTTAT T C RAVER1 Ensembl:ENSG00000161847 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs281422 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38589,RMVar_hsa_circ_51169 24291 RMVar_ID_24291 Human_SNP_ID_658165911 A-to-I Human chr19 - 10326011 10326011 10326011 CTTCAGGTGATACACCTGCCTCGGCCTCCCCAAGTGCTGAGATTACAGGTGTGAGCCACTGCGCT CTTCAGGTGATACACCTGCCTCGGCCTCCCCAGGTGCTGAGATTACAGGTGTGAGCCACTGCGCT T C RAVER1 Ensembl:ENSG00000161847 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs188324234 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38589,RMVar_hsa_circ_51169 24292 RMVar_ID_24292 Human_SNP_ID_658167314 A-to-I Human chr19 - 10330978 10330978 10330978 CACACTGCAACCTCTGCCTCCTGGGTGCAAGCAGTTCTCCTACCTCAGCCTCCCGAGTAGCTAGG CACACTGCAACCTCTGCCTCCTGGGTGCAAGCCGTTCTCCTACCTCAGCCTCCCGAGTAGCTAGG T G RAVER1 Ensembl:ENSG00000161847 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1289565801 Functional Loss SNV dbSNP153 33..33 33 - - - 24293 RMVar_ID_24293 Human_SNP_ID_658173127 A-to-I Human chr19 - 10349848 10349848 10349848 AGTGCTTAATAAATATACAATATTGGCCGGGCACGGCAGCTCACGCCTGTAATCCCAGCACTTTG AGTGCTTAATAAATATACAATATTGGCCGGGCGCGGCAGCTCACGCCTGTAATCCCAGCACTTTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs570985320 Functional Loss SNV dbSNP153 33..33 33 - - - 24294 RMVar_ID_24294 Human_SNP_ID_658173582 A-to-I Human chr19 - 10351440 10351440 10351440 ACTTGTATCCCAGGCTGGAGTGCAATGGCACAATCTCGGCTCACTGCAACCTCCGCCTCCCAGGT ACTTGTATCCCAGGCTGGAGTGCAATGGCACAGTCTCGGCTCACTGCAACCTCCGCCTCCCAGGT T C TYK2 Ensembl:ENSG00000105397 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1422819773 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1954528 24295 RMVar_ID_24295 Human_SNP_ID_658173672 A-to-I Human chr19 - 10351801 10351801 10351801 CCGGTAGGCGAAGGTTGCAGTGAGCCGAGATCATGCCACTGCACTCCAGCCTGGGTGAAAGAGCG CCGGTAGGCGAAGGTTGCAGTGAGCCGAGATCGTGCCACTGCACTCCAGCCTGGGTGAAAGAGCG T C TYK2 Ensembl:ENSG00000105397 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs927483881 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9908345,Human_RBP_ID_22978294,Human_RBP_ID_25441744 24296 RMVar_ID_24296 Human_SNP_ID_658173676 A-to-I Human chr19 - 10351822 10351821 10351822 GGCAGGGAGAATTGCTTGAACCCGGTAGGCGAAGGTTGCAGTGAGCCGAGATCATGCCACTGCAC GGCAGGGAGAATTGCTTGAACCCGGTAGGCGA_GGTTGCAGTGAGCCGAGATCATGCCACTGCAC CT C TYK2 Ensembl:ENSG00000105397 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1402239440 Functional Loss DEL dbSNP153 33..33 33 - - - 24297 RMVar_ID_24297 Human_SNP_ID_658173677 A-to-I Human chr19 - 10351822 10351822 10351822 GGCAGGGAGAATTGCTTGAACCCGGTAGGCGAAGGTTGCAGTGAGCCGAGATCATGCCACTGCAC GGCAGGGAGAATTGCTTGAACCCGGTAGGCGAGGGTTGCAGTGAGCCGAGATCATGCCACTGCAC T C TYK2 Ensembl:ENSG00000105397 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1266138825 Functional Loss SNV dbSNP153 33..33 33 - - - 24298 RMVar_ID_24298 Human_SNP_ID_658173704 A-to-I Human chr19 - 10351877 10351877 10351877 AAATTAGCCGGGCGTGGTGGCAGGTGCCTGTAATCCCAGCTACTCAGGCGGCTGAGGCAGGGAGA AAATTAGCCGGGCGTGGTGGCAGGTGCCTGTAGTCCCAGCTACTCAGGCGGCTGAGGCAGGGAGA T C TYK2 Ensembl:ENSG00000105397 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1442715086 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_139712 24299 RMVar_ID_24299 Human_SNP_ID_658173863 A-to-I Human chr19 - 10352352 10352350 10352352 AAGGCATAGGCTGGGCCAGGCGCGGTGGCTCAAGCCTGTAATCCCAGCACTTTGGGAGGCCGAGG AAGGCATAGGCTGGGCCAGGCGCGGTGGCTCA__CCTGTAATCCCAGCACTTTGGGAGGCCGAGG GCT G TYK2 Ensembl:ENSG00000105397 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1472129126 Functional Loss DEL dbSNP153 33..34 33 - - - 24300 RMVar_ID_24300 Human_SNP_ID_658173865 A-to-I Human chr19 - 10352352 10352352 10352352 AAGGCATAGGCTGGGCCAGGCGCGGTGGCTCAAGCCTGTAATCCCAGCACTTTGGGAGGCCGAGG AAGGCATAGGCTGGGCCAGGCGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGG T A TYK2 Ensembl:ENSG00000105397 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs919130116 Functional Loss SNV dbSNP153 33..33 33 - - - 24301 RMVar_ID_24301 Human_SNP_ID_658175910 A-to-I Human chr19 - 10358830 10358830 10358830 TCGAACTTCTGACCTCGTGATCCATCCGCCTCAGCCTCCCAAAGTGCTGGGATTCCAGGCGTGAG TCGAACTTCTGACCTCGTGATCCATCCGCCTCGGCCTCCCAAAGTGCTGGGATTCCAGGCGTGAG T C TYK2 Ensembl:ENSG00000105397 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs924430299 Functional Loss SNV dbSNP153 33..33 33 - - - 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 24302 RMVar_ID_24302 Human_SNP_ID_658176492 A-to-I Human chr19 - 10360891 10360891 10360891 AATCAGGGCCAGGCATGGTGACCTATGCCTGTAGTCCTAGCTACTTGTGAGGCTGGAATGGAAGG AATCAGGGCCAGGCATGGTGACCTATGCCTGTGGTCCTAGCTACTTGTGAGGCTGGAATGGAAGG T C TYK2 Ensembl:ENSG00000105397 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs940705957 Functional Loss SNV dbSNP153 33..33 33 - - - 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_336536 24303 RMVar_ID_24303 Human_SNP_ID_658177572 A-to-I Human chr19 - 10364314 10364314 10364314 TAGAGATGGGGTTTCATCAGATTGGCCAACCTAGTCTTGAACTCCTGACCTCAGGTGATCCACCC TAGAGATGGGGTTTCATCAGATTGGCCAACCTGGTCTTGAACTCCTGACCTCAGGTGATCCACCC T C TYK2 Ensembl:ENSG00000105397 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs991723953 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88271,RMVar_hsa_circ_82488,RMVar_hsa_circ_192345,RMVar_hsa_circ_192348,RMVar_hsa_circ_79351,RMVar_hsa_circ_192347 24304 RMVar_ID_24304 Human_SNP_ID_658179600 A-to-I Human chr19 - 10370736 10370736 10370736 CTCGGCTCACTGCAACCTCTGCCTCCAGGTTCAAGCAATTCTCTTGCCTCAGCCTGCTGAGTAGC CTCGGCTCACTGCAACCTCTGCCTCCAGGTTCGAGCAATTCTCTTGCCTCAGCCTGCTGAGTAGC T C TYK2 Ensembl:ENSG00000105397 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs891514173 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88271,RMVar_hsa_circ_192345 24305 RMVar_ID_24305 Human_SNP_ID_658179812 A-to-I Human chr19 - 10371631 10371630 10371632 TTTACAGTTCATAACTTTTTTTTTTTTGAGACAGAGTTTCGCTCCTGTTGCCCAGGTTGGAGTGC TTTACAGTTCATAACTTTTTTTTTTTTGAGA__GAGTTTCGCTCCTGTTGCCCAGGTTGGAGTGC CTG C TYK2 Ensembl:ENSG00000105397 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1375654123 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_88271,RMVar_hsa_circ_192345 24306 RMVar_ID_24306 Human_SNP_ID_658180501 A-to-I Human chr19 - 10373603 10373603 10373603 TCTCAAGCCAGGCACAGTGGGTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGCAGA TCTCAAGCCAGGCACAGTGGGTCACGCCTGTATTCCCAGCACTTTGGGAGGCTGAGGCGGGCAGA T A TYK2 Ensembl:ENSG00000105397 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1445739823 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88271,RMVar_hsa_circ_192345 24307 RMVar_ID_24307 Human_SNP_ID_658201902 A-to-I Human chr19 + 10449391 10449387 10449391 TTGTTTGTTTGTTTGTTTTGAGATCAAGTCTCACTCTGTCACACAGGCTGGAGTGCAGTAGTGCG TTGTTTGTTTGTTTGTTTTGAGATCAAGT____CTCTGTCACACAGGCTGGAGTGCAGTAGTGCG TCTCA T PDE4A Ensembl:ENSG00000065989 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1309854742 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_31411,RMVar_hsa_circ_22508,RMVar_hsa_circ_340540,RMVar_hsa_circ_84101,RMVar_hsa_circ_192362,RMVar_hsa_circ_70952,RMVar_hsa_circ_192364 24308 RMVar_ID_24308 Human_SNP_ID_658209868 A-to-I Human chr19 - 10476683 10476683 10476683 CAACATGGTGAAACCCCATCTCTACTAAAAATAAAAAAATTAGCCGGGCGTGGTGGTGGGTGCCT CAACATGGTGAAACCCCATCTCTACTAAAAATTAAAAAATTAGCCGGGCGTGGTGGTGGGTGCCT T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1050051883 Functional Loss SNV dbSNP153 33..33 33 - - - 24309 RMVar_ID_24309 Human_SNP_ID_658214016 A-to-I Human chr19 - 10490452 10490452 10490452 AAATTAGCCGGGCGTGGTGGTGGGTGCCTGTTATCCCAGCTACTTGTGAGGCTGAGGCTGAATAA AAATTAGCCGGGCGTGGTGGTGGGTGCCTGTTTTCCCAGCTACTTGTGAGGCTGAGGCTGAATAA T A AC011461.1,KEAP1 Ensembl:ENSG00000267197,Ensembl:ENSG00000079999 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs774725220 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5249060 RMVar_hsa_circ_192369,RMVar_hsa_circ_291691 24310 RMVar_ID_24310 Human_SNP_ID_658214682 A-to-I Human chr19 - 10492857 10492856 10492858 AGATCATGCCACTGCACTCCAGCCTGGGTGACAGAGTGAGACTCTGTCTCAAAAACCAAAGCCAA AGATCATGCCACTGCACTCCAGCCTGGGTGA__GAGTGAGACTCTGTCTCAAAAACCAAAGCCAA CTG C KEAP1 Ensembl:ENSG00000079999 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1568399096 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_87608,RMVar_hsa_circ_192373 24311 RMVar_ID_24311 Human_SNP_ID_658215479 A-to-I Human chr19 - 10495506 10495506 10495506 TTTAGTAGAGACGGGGTTTCACCGTGTTGGCCAGGCTGGTCTCGGACTTCTGACCTCAGGTGATC TTTAGTAGAGACGGGGTTTCACCGTGTTGGCCTGGCTGGTCTCGGACTTCTGACCTCAGGTGATC T A KEAP1 Ensembl:ENSG00000079999 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1212997433 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87608,RMVar_hsa_circ_192373 24312 RMVar_ID_24312 Human_SNP_ID_658215776 A-to-I Human chr19 - 10496567 10496567 10496567 GAACTCCTTACCTCACGTGATCCGCCCACCTCAGCCTCCCAAAGTGTTGGGATTACAGGCTTGAG GAACTCCTTACCTCACGTGATCCGCCCACCTCGGCCTCCCAAAGTGTTGGGATTACAGGCTTGAG T C KEAP1 Ensembl:ENSG00000079999 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1258061697 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87608,RMVar_hsa_circ_192373 24313 RMVar_ID_24313 Human_SNP_ID_658215835 A-to-I Human chr19 - 10496783 10496783 10496783 CCTTTTTTGTTTTTGAGACTGAGTCTGGCTCTATCGCCCAGGCTGAAGTGCAGTGGCAAGATTTC CCTTTTTTGTTTTTGAGACTGAGTCTGGCTCTGTCGCCCAGGCTGAAGTGCAGTGGCAAGATTTC T C KEAP1 Ensembl:ENSG00000079999 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs753780555 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87608,RMVar_hsa_circ_192373 24314 RMVar_ID_24314 Human_SNP_ID_658216051 A-to-I Human chr19 - 10497811 10497811 10497811 TAGCTCACTGTAGCCTCCAACTCTTGGGCTCAAGGAGGCCTCCTATCTCAGCCTCCTGAGTAGCT TAGCTCACTGTAGCCTCCAACTCTTGGGCTCAGGGAGGCCTCCTATCTCAGCCTCCTGAGTAGCT T C KEAP1 Ensembl:ENSG00000079999 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1218381862 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87608,RMVar_hsa_circ_192373 24315 RMVar_ID_24315 Human_SNP_ID_658216110 A-to-I Human chr19 - 10498038 10498038 10498038 AAATTAGCCTGGCATGGTGGCTCATGCTTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAA AAATTAGCCTGGCATGGTGGCTCATGCTTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAA T C KEAP1 Ensembl:ENSG00000079999 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1274148934 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87608,RMVar_hsa_circ_192373 24316 RMVar_ID_24316 Human_SNP_ID_658216111 A-to-I Human chr19 - 10498038 10498038 10498038 AAATTAGCCTGGCATGGTGGCTCATGCTTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAA AAATTAGCCTGGCATGGTGGCTCATGCTTGTACTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAA T G KEAP1 Ensembl:ENSG00000079999 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1274148934 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87608,RMVar_hsa_circ_192373 24317 RMVar_ID_24317 Human_SNP_ID_658216126 A-to-I Human chr19 - 10498103 10498103 10498103 CTGCGGTCGGGAGTTCAAGACCAGCCTGACCAACATGGAGAAACCACGTCTCTATTAAAAATGCA CTGCGGTCGGGAGTTCAAGACCAGCCTGACCAGCATGGAGAAACCACGTCTCTATTAAAAATGCA T C KEAP1 Ensembl:ENSG00000079999 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1401978616 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87608,RMVar_hsa_circ_192373 24318 RMVar_ID_24318 Human_SNP_ID_658217039 A-to-I Human chr19 - 10501518 10501518 10501518 TCACGCCTTTCTCCCGCCTCAGCCTCCCATGTAGCTGGGACTACAGGCGCCCGCCGCCACACCCG TCACGCCTTTCTCCCGCCTCAGCCTCCCATGTTGCTGGGACTACAGGCGCCCGCCGCCACACCCG T A KEAP1 Ensembl:ENSG00000079999 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs953877992 Functional Loss SNV dbSNP153 33..33 33 - - - 24319 RMVar_ID_24319 Human_SNP_ID_658217040 A-to-I Human chr19 - 10501518 10501518 10501518 TCACGCCTTTCTCCCGCCTCAGCCTCCCATGTAGCTGGGACTACAGGCGCCCGCCGCCACACCCG TCACGCCTTTCTCCCGCCTCAGCCTCCCATGTCGCTGGGACTACAGGCGCCCGCCGCCACACCCG T G KEAP1 Ensembl:ENSG00000079999 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs953877992 Functional Loss SNV dbSNP153 33..33 33 - - - 24320 RMVar_ID_24320 Human_SNP_ID_658230544 A-to-I Human chr19 + 10547507 10547505 10547507 GACATAAGGCCAGGTGTGGTGGCACATACTGTAGTCTCAGCTACTTGGGAGGCTGAGGTGGGAGG GACATAAGGCCAGGTGTGGTGGCACATACTG__GTCTCAGCTACTTGGGAGGCTGAGGTGGGAGG GTA G ATG4D Ensembl:ENSG00000130734 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs983434738 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_6717209 RMVar_hsa_circ_16077,RMVar_hsa_circ_73867,RMVar_hsa_circ_122758,RMVar_hsa_circ_192375 24321 RMVar_ID_24321 Human_SNP_ID_658232361 A-to-I Human chr19 - 10553145 10553145 10553145 GGCTGACAACAGGAAGTACCATCATCACTGCCAGAGCTCAAGATCCCACACCCGACATGACATAA GGCTGACAACAGGAAGTACCATCATCACTGCCGGAGCTCAAGATCCCACACCCGACATGACATAA T C KRI1 Ensembl:ENSG00000129347 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350441670 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_55258,Human_RBP_ID_279173,Human_RBP_ID_1879510,Human_RBP_ID_3562324,Human_RBP_ID_4498606,Human_RBP_ID_8476223,Human_RBP_ID_13358374,Human_RBP_ID_17266525,Human_RBP_ID_18721428,Human_RBP_ID_26471978,Human_RBP_ID_27266930,Human_RBP_ID_27462786 24322 RMVar_ID_24322 Human_SNP_ID_658239405 A-to-I Human chr19 - 10573857 10573857 10573857 CAGGAGTTCCAGACCAGCCTTGGCAACACAGCAAAACCCCTTCACTACAAAAAATATAAAAATTA CAGGAGTTCCAGACCAGCCTTGGCAACACAGCGAAACCCCTTCACTACAAAAAATATAAAAATTA T C AP1M2 Ensembl:ENSG00000129354 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1313181116 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127146,RMVar_hsa_circ_192381,RMVar_hsa_circ_117008,RMVar_hsa_circ_192380 24323 RMVar_ID_24323 Human_SNP_ID_658249390 A-to-I Human chr19 + 10608275 10608275 10608275 GAGAGACAGGGTCTTGCTATGTTGCCTTGGCTAGCCTAGAACTCCTGAGTTGAAGGGATCCTCCC GAGAGACAGGGTCTTGCTATGTTGCCTTGGCTTGCCTAGAACTCCTGAGTTGAAGGGATCCTCCC A T SLC44A2 Ensembl:ENSG00000129353 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1568441511 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79148,RMVar_hsa_circ_192386 24324 RMVar_ID_24324 Human_SNP_ID_658249752 A-to-I Human chr19 + 10609480 10609480 10609480 CCTCACCACGTCCAGCTACTTTTTGTATTTTTAGTAGAGACTGGGTTTTGCCATGTTTGTCAGGC CCTCACCACGTCCAGCTACTTTTTGTATTTTTGGTAGAGACTGGGTTTTGCCATGTTTGTCAGGC A G SLC44A2 Ensembl:ENSG00000129353 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1216476042 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79148,RMVar_hsa_circ_192386 24325 RMVar_ID_24325 Human_SNP_ID_658250852 A-to-I Human chr19 + 10613591 10613591 10613591 GACTTTGGCTGGGTGTAGTGGCTCATGCCTGTAGTTCAAGCACTTTGGGAGGCTAAGGCAGGAGG GACTTTGGCTGGGTGTAGTGGCTCATGCCTGTTGTTCAAGCACTTTGGGAGGCTAAGGCAGGAGG A T SLC44A2 Ensembl:ENSG00000129353 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1387560019 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79148,RMVar_hsa_circ_192386 24326 RMVar_ID_24326 Human_SNP_ID_658254393 A-to-I Human chr19 + 10626531 10626531 10626531 CGCCTCCCGGGTTCGAGCAATTCTCCCACCTCAGTCTCCCAAGTAGCTGGGATTACAGGCTTGCA CGCCTCCCGGGTTCGAGCAATTCTCCCACCTCTGTCTCCCAAGTAGCTGGGATTACAGGCTTGCA A T SLC44A2 Ensembl:ENSG00000129353 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs940992497 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1804,RMVar_hsa_circ_78723,RMVar_hsa_circ_79148,RMVar_hsa_circ_192386,RMVar_hsa_circ_307206,RMVar_hsa_circ_347867,RMVar_hsa_circ_192387,RMVar_hsa_circ_376198,RMVar_hsa_circ_319789,RMVar_hsa_circ_14303,RMVar_hsa_circ_192388,RMVar_hsa_circ_192389,RMVar_hsa_circ_192390 24327 RMVar_ID_24327 Human_SNP_ID_658254571 A-to-I Human chr19 + 10627198 10627198 10627198 CAAGAATTAGCTGGGCATGGTGGCGGGCACCTATAATCCCAGCTACTTGGGAGACTGAGGCAGGA CAAGAATTAGCTGGGCATGGTGGCGGGCACCTGTAATCCCAGCTACTTGGGAGACTGAGGCAGGA A G SLC44A2 Ensembl:ENSG00000129353 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1182657788 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1804,RMVar_hsa_circ_78723,RMVar_hsa_circ_79148,RMVar_hsa_circ_192386,RMVar_hsa_circ_307206,RMVar_hsa_circ_347867,RMVar_hsa_circ_192387,RMVar_hsa_circ_376198,RMVar_hsa_circ_319789,RMVar_hsa_circ_14303,RMVar_hsa_circ_192388,RMVar_hsa_circ_192389,RMVar_hsa_circ_192390 24328 RMVar_ID_24328 Human_SNP_ID_658255377 A-to-I Human chr19 + 10629847 10629847 10629847 GCGATCTTGGCTCACTGCAACCTCCGCCACCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTA GCGATCTTGGCTCACTGCAACCTCCGCCACCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTA A G SLC44A2 Ensembl:ENSG00000129353 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs951677925 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1804,RMVar_hsa_circ_78723,RMVar_hsa_circ_79148,RMVar_hsa_circ_192386,RMVar_hsa_circ_347867,RMVar_hsa_circ_192387,RMVar_hsa_circ_376198,RMVar_hsa_circ_319789,RMVar_hsa_circ_14303,RMVar_hsa_circ_75772,RMVar_hsa_circ_192389,RMVar_hsa_circ_192390,RMVar_hsa_circ_16073,RMVar_hsa_circ_192392 24329 RMVar_ID_24329 Human_SNP_ID_658255382 A-to-I Human chr19 + 10629879 10629879 10629879 AGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTAAGTAGCTGGGATTACAGGTGCCCGCCACCACA AGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGTGCCCGCCACCACA A G SLC44A2 Ensembl:ENSG00000129353 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs202170452 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1804,RMVar_hsa_circ_78723,RMVar_hsa_circ_79148,RMVar_hsa_circ_192386,RMVar_hsa_circ_347867,RMVar_hsa_circ_192387,RMVar_hsa_circ_376198,RMVar_hsa_circ_319789,RMVar_hsa_circ_14303,RMVar_hsa_circ_75772,RMVar_hsa_circ_192389,RMVar_hsa_circ_192390,RMVar_hsa_circ_16073,RMVar_hsa_circ_192392 24330 RMVar_ID_24330 Human_SNP_ID_658255383 A-to-I Human chr19 + 10629895 10629895 10629895 CCTGCCTCAGCCTCCTAAGTAGCTGGGATTACAGGTGCCCGCCACCACACCCAGCTAATTTTTTG CCTGCCTCAGCCTCCTAAGTAGCTGGGATTACGGGTGCCCGCCACCACACCCAGCTAATTTTTTG A G SLC44A2 Ensembl:ENSG00000129353 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1275443790 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1804,RMVar_hsa_circ_78723,RMVar_hsa_circ_79148,RMVar_hsa_circ_192386,RMVar_hsa_circ_347867,RMVar_hsa_circ_192387,RMVar_hsa_circ_376198,RMVar_hsa_circ_319789,RMVar_hsa_circ_14303,RMVar_hsa_circ_75772,RMVar_hsa_circ_192389,RMVar_hsa_circ_192390,RMVar_hsa_circ_16073,RMVar_hsa_circ_192392 24331 RMVar_ID_24331 Human_SNP_ID_658256599 A-to-I Human chr19 + 10633369 10633369 10633369 TTGTATTTTTAGTAGAGATGGGGTTTTACCATATTGGCCAGGCTGGTCTCGACTTCCTCGTGATC TTGTATTTTTAGTAGAGATGGGGTTTTACCATCTTGGCCAGGCTGGTCTCGACTTCCTCGTGATC A C SLC44A2 Ensembl:ENSG00000129353 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1225483535 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1850,RMVar_hsa_circ_79148,RMVar_hsa_circ_192386,RMVar_hsa_circ_347867,RMVar_hsa_circ_376198,RMVar_hsa_circ_319789,RMVar_hsa_circ_75772,RMVar_hsa_circ_192389,RMVar_hsa_circ_192390,RMVar_hsa_circ_192392,RMVar_hsa_circ_60818,RMVar_hsa_circ_192396,RMVar_hsa_circ_78359,RMVar_hsa_circ_109377,RMVar_hsa_circ_192397,RMVar_hsa_circ_97561,RMVar_hsa_circ_375359,RMVar_hsa_circ_192399,RMVar_hsa_circ_192400 24332 RMVar_ID_24332 Human_SNP_ID_658256891 A-to-I Human chr19 + 10634370 10634370 10634370 CCTGTAATCCCAGCTGCTCGGGAAGCTGAGGCAGGAGAATCGCTTGAACCCGTGAAGTGGAGGTT CCTGTAATCCCAGCTGCTCGGGAAGCTGAGGCGGGAGAATCGCTTGAACCCGTGAAGTGGAGGTT A G SLC44A2 Ensembl:ENSG00000129353 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1197200169 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1850,RMVar_hsa_circ_79148,RMVar_hsa_circ_192386,RMVar_hsa_circ_347867,RMVar_hsa_circ_376198,RMVar_hsa_circ_319789,RMVar_hsa_circ_75772,RMVar_hsa_circ_192389,RMVar_hsa_circ_192390,RMVar_hsa_circ_192392,RMVar_hsa_circ_60818,RMVar_hsa_circ_192396,RMVar_hsa_circ_78359,RMVar_hsa_circ_109377,RMVar_hsa_circ_192397,RMVar_hsa_circ_97561,RMVar_hsa_circ_375359,RMVar_hsa_circ_192399,RMVar_hsa_circ_192400 24333 RMVar_ID_24333 Human_SNP_ID_658258416 A-to-I Human chr19 + 10639168 10639168 10639168 GTTGGCTGGGCTGGTCTCAAACTCCTGACCTCAAGTGATCCGCCCGCCTCGGGCTCGCAGAGTAC GTTGGCTGGGCTGGTCTCAAACTCCTGACCTCTAGTGATCCGCCCGCCTCGGGCTCGCAGAGTAC A T SLC44A2 Ensembl:ENSG00000129353 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1300438169 Functional Loss SNV dbSNP153 33..33 33 - - - 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_192407 24334 RMVar_ID_24334 Human_SNP_ID_658258842 A-to-I Human chr19 + 10640926 10640926 10640926 GGCTAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAAAATTAGTCAGGTGTGCTGGTACG GGCTAACATGGTGAAACCCCATCTCTACTAAACATACAAAAAAATTAGTCAGGTGTGCTGGTACG A C SLC44A2 Ensembl:ENSG00000129353 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1172243240 Functional Loss SNV dbSNP153 33..33 33 - - - 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_192407 24335 RMVar_ID_24335 Human_SNP_ID_658258962 A-to-I Human chr19 + 10641255 10641255 10641255 TCTCCACAAAAAAATACAAAAATTAGCTGGGTATGCTGGAACATGCCTGTAGTCCCAGCTCCTTG TCTCCACAAAAAAATACAAAAATTAGCTGGGTGTGCTGGAACATGCCTGTAGTCCCAGCTCCTTG A G SLC44A2 Ensembl:ENSG00000129353 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs771532407 Functional Loss SNV dbSNP153 33..33 33 - - - 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_192407 24336 RMVar_ID_24336 Human_SNP_ID_658264343 A-to-I Human chr19 + 10656943 10656943 10656943 CTCCTGCCTCAGCCTCCCGAGTAGCTGGAATTACAGGCATGCTCCACTACACCTAGCTAATTTTG CTCCTGCCTCAGCCTCCCGAGTAGCTGGAATTGCAGGCATGCTCCACTACACCTAGCTAATTTTG A G ILF3 Ensembl:ENSG00000129351 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1398184370 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1291912 24337 RMVar_ID_24337 Human_SNP_ID_658264515 A-to-I Human chr19 + 10657547 10657547 10657547 ATTGGTGGCCGGGTGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGCGG ATTGGTGGCCGGGTGCGGTGGCTCACGCCTGTTATCCCAGCACTTTGGGAGGCTGAGGTGGGCGG A T ILF3 Ensembl:ENSG00000129351 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1007449460 Functional Loss SNV dbSNP153 33..33 33 - - - 24338 RMVar_ID_24338 Human_SNP_ID_658264695 A-to-I Human chr19 + 10658063 10658063 10658063 GGAACCACAGGCACATGTCACCACACCCAGCTAATTTTTTGAATTTTTTGTAGAGACAGGATCTT GGAACCACAGGCACATGTCACCACACCCAGCTGATTTTTTGAATTTTTTGTAGAGACAGGATCTT A G ILF3 Ensembl:ENSG00000129351 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1463894061 Functional Loss SNV dbSNP153 33..33 33 - - - 24339 RMVar_ID_24339 Human_SNP_ID_658264705 A-to-I Human chr19 + 10658088 10658088 10658088 CCCAGCTAATTTTTTGAATTTTTTGTAGAGACAGGATCTTTCCACGTTGCCCAGGCTGGCCTCAG CCCAGCTAATTTTTTGAATTTTTTGTAGAGACGGGATCTTTCCACGTTGCCCAGGCTGGCCTCAG A G ILF3 Ensembl:ENSG00000129351 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1219951743 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6717308,Human_RBP_ID_13358761,Human_RBP_ID_23173504,Human_RBP_ID_25381379 24340 RMVar_ID_24340 Human_SNP_ID_658264706 A-to-I Human chr19 + 10658088 10658088 10658088 CCCAGCTAATTTTTTGAATTTTTTGTAGAGACAGGATCTTTCCACGTTGCCCAGGCTGGCCTCAG CCCAGCTAATTTTTTGAATTTTTTGTAGAGACTGGATCTTTCCACGTTGCCCAGGCTGGCCTCAG A T ILF3 Ensembl:ENSG00000129351 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1219951743 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6717308,Human_RBP_ID_13358761,Human_RBP_ID_23173504,Human_RBP_ID_25381379 24341 RMVar_ID_24341 Human_SNP_ID_658264720 A-to-I Human chr19 + 10658138 10658138 10658138 CCAGGCTGGCCTCAGAACTCTTGGGCTCAAGCAATCTGCCCACCTTGGCCTCCCAAAAAGCTGGA CCAGGCTGGCCTCAGAACTCTTGGGCTCAAGCGATCTGCCCACCTTGGCCTCCCAAAAAGCTGGA A G ILF3 Ensembl:ENSG00000129351 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs892828015 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13358762 24342 RMVar_ID_24342 Human_SNP_ID_658264791 A-to-I Human chr19 + 10658395 10658395 10658395 ATCCTCCTGCAGCCTCTCAAAGTGCTGGGATTACAGATATGAGCCGCCTTGCCCAGTGGCACTAA ATCCTCCTGCAGCCTCTCAAAGTGCTGGGATTGCAGATATGAGCCGCCTTGCCCAGTGGCACTAA A G ILF3 Ensembl:ENSG00000129351 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs899127161 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13358789,Human_RBP_ID_18721476 24343 RMVar_ID_24343 Human_SNP_ID_658264845 A-to-I Human chr19 + 10658584 10658584 10658584 ATAATTTTAAGTGATAGTAAGAAGTTCTGGCCAGGCGCGGTGGCTCAGGCCTGTAATCCCAGAAC ATAATTTTAAGTGATAGTAAGAAGTTCTGGCCTGGCGCGGTGGCTCAGGCCTGTAATCCCAGAAC A T ILF3 Ensembl:ENSG00000129351 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1297711294 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13358800,Human_RBP_ID_25381388 24344 RMVar_ID_24344 Human_SNP_ID_658265059 A-to-I Human chr19 + 10659155 10659155 10659155 TGGAGTGCAGTGGCACGGTCTCGGCTTACTGCAACCTCCGCCTCCTGGGTTCAAGTGTTTCTCTT TGGAGTGCAGTGGCACGGTCTCGGCTTACTGCCACCTCCGCCTCCTGGGTTCAAGTGTTTCTCTT A C ILF3 Ensembl:ENSG00000129351 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1253779517 Functional Loss SNV dbSNP153 33..33 33 - - - 24345 RMVar_ID_24345 Human_SNP_ID_658265114 A-to-I Human chr19 + 10659305 10659305 10659305 TAGAGATGAGGTTTCACCATTTTGCTCGGGCTAGTCTCGAATACCTGACCTCAAGTGATCTGCTG TAGAGATGAGGTTTCACCATTTTGCTCGGGCTGGTCTCGAATACCTGACCTCAAGTGATCTGCTG A G ILF3 Ensembl:ENSG00000129351 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1335583355 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13358828,Human_RBP_ID_23173519,Human_RBP_ID_23309170 24346 RMVar_ID_24346 Human_SNP_ID_658265726 A-to-I Human chr19 + 10661123 10661123 10661123 TTATTTCTGGCTGGGCGCGGTGGTTCACGCCTATAATCCCAGCACTTTGGGAGGCCGAGGCTGGC TTATTTCTGGCTGGGCGCGGTGGTTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCTGGC A G ILF3 Ensembl:ENSG00000129351 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs570945681 Functional Loss SNV dbSNP153 33..33 33 - - - 24347 RMVar_ID_24347 Human_SNP_ID_658265727 A-to-I Human chr19 + 10661125 10661125 10661125 ATTTCTGGCTGGGCGCGGTGGTTCACGCCTATAATCCCAGCACTTTGGGAGGCCGAGGCTGGCGG ATTTCTGGCTGGGCGCGGTGGTTCACGCCTATGATCCCAGCACTTTGGGAGGCCGAGGCTGGCGG A G ILF3 Ensembl:ENSG00000129351 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs953811298 Functional Loss SNV dbSNP153 33..33 33 - - - 24348 RMVar_ID_24348 Human_SNP_ID_658265754 A-to-I Human chr19 + 10661225 10661225 10661225 CAACATGGTGAAATCCCGTCTGTACTAAAAATACAAAAATTAGCCAGGAATGGTGGTCTGTGGCT CAACATGGTGAAATCCCGTCTGTACTAAAAATGCAAAAATTAGCCAGGAATGGTGGTCTGTGGCT A G ILF3 Ensembl:ENSG00000129351 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs61232098 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13358928 24349 RMVar_ID_24349 Human_SNP_ID_658265759 A-to-I Human chr19 + 10661238 10661238 10661238 TCCCGTCTGTACTAAAAATACAAAAATTAGCCAGGAATGGTGGTCTGTGGCTGTAATCCCAGTTA TCCCGTCTGTACTAAAAATACAAAAATTAGCCTGGAATGGTGGTCTGTGGCTGTAATCCCAGTTA A T ILF3 Ensembl:ENSG00000129351 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1409374669 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13358928 24350 RMVar_ID_24350 Human_SNP_ID_658265779 A-to-I Human chr19 + 10661287 10661286 10661288 GCTGTAATCCCAGTTACTCAGTAGAGTGAGGCAGAAGAATTGCTTGAACCCACGAGGCGGAAGTT GCTGTAATCCCAGTTACTCAGTAGAGTGAGGC__AAGAATTGCTTGAACCCACGAGGCGGAAGTT CAG C ILF3 Ensembl:ENSG00000129351 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1263759953 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_13358930 24351 RMVar_ID_24351 Human_SNP_ID_658265780 A-to-I Human chr19 + 10661287 10661287 10661287 GCTGTAATCCCAGTTACTCAGTAGAGTGAGGCAGAAGAATTGCTTGAACCCACGAGGCGGAAGTT GCTGTAATCCCAGTTACTCAGTAGAGTGAGGCGGAAGAATTGCTTGAACCCACGAGGCGGAAGTT A G ILF3 Ensembl:ENSG00000129351 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs58008110 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13358930 24352 RMVar_ID_24352 Human_SNP_ID_658265788 A-to-I Human chr19 + 10661306 10661306 10661306 AGTAGAGTGAGGCAGAAGAATTGCTTGAACCCACGAGGCGGAAGTTGCAGTTGAGCTGAGATCAC AGTAGAGTGAGGCAGAAGAATTGCTTGAACCCGCGAGGCGGAAGTTGCAGTTGAGCTGAGATCAC A G ILF3 Ensembl:ENSG00000129351 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs74180164 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13358932 24353 RMVar_ID_24353 Human_SNP_ID_658265952 A-to-I Human chr19 + 10661711 10661711 10661711 CCACCACACCGGGCTAATTTTGTATTTTTAGTAGAGATGGAGTTTCTCCAAGTTGGTCAGGCCGG CCACCACACCGGGCTAATTTTGTATTTTTAGTGGAGATGGAGTTTCTCCAAGTTGGTCAGGCCGG A G ILF3 Ensembl:ENSG00000129351 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1357687612 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13358945 24354 RMVar_ID_24354 Human_SNP_ID_658265958 A-to-I Human chr19 + 10661728 10661728 10661728 TTTTGTATTTTTAGTAGAGATGGAGTTTCTCCAAGTTGGTCAGGCCGGTCTGGAACTCCCAACCT TTTTGTATTTTTAGTAGAGATGGAGTTTCTCCCAGTTGGTCAGGCCGGTCTGGAACTCCCAACCT A C ILF3 Ensembl:ENSG00000129351 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs938296855 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13358945,Human_RBP_ID_23173535,Human_RBP_ID_25381444 24355 RMVar_ID_24355 Human_SNP_ID_658265959 A-to-I Human chr19 + 10661728 10661728 10661728 TTTTGTATTTTTAGTAGAGATGGAGTTTCTCCAAGTTGGTCAGGCCGGTCTGGAACTCCCAACCT TTTTGTATTTTTAGTAGAGATGGAGTTTCTCCGAGTTGGTCAGGCCGGTCTGGAACTCCCAACCT A G ILF3 Ensembl:ENSG00000129351 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs938296855 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13358945,Human_RBP_ID_23173535,Human_RBP_ID_25381444 24356 RMVar_ID_24356 Human_SNP_ID_658266689 A-to-I Human chr19 + 10664112 10664112 10664112 ACTTAGGCCGGGGGCAGTGGCTCACTGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGCAG ACTTAGGCCGGGGGCAGTGGCTCACTGCCTGTGATCCCAGCACTTTGGGAGGCCGAGGTGGGCAG A G ILF3 Ensembl:ENSG00000129351 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs964009709 Functional Loss SNV dbSNP153 33..33 33 - - - 24357 RMVar_ID_24357 Human_SNP_ID_658266827 A-to-I Human chr19 + 10664498 10664498 10664498 GTCAGGAGTTCGAGACCAGCCTGACAAATGTGATGAAACCCCGTCTCTACTAAAAATACAAAAAA GTCAGGAGTTCGAGACCAGCCTGACAAATGTGGTGAAACCCCGTCTCTACTAAAAATACAAAAAA A G ILF3 Ensembl:ENSG00000129351 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1308624894 Functional Loss SNV dbSNP153 33..33 33 - - - 24358 RMVar_ID_24358 Human_SNP_ID_658266852 A-to-I Human chr19 + 10664562 10664562 10664562 AAAATTAGCCAGGTGTGGTGGTGCATGTCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGACA AAAATTAGCCAGGTGTGGTGGTGCATGTCTGTGATCCCAGCTACTTGGGAGGCTGAGGCAGGACA A G ILF3 Ensembl:ENSG00000129351 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1294887085 Functional Loss SNV dbSNP153 33..33 33 - - - 24359 RMVar_ID_24359 Human_SNP_ID_658267592 A-to-I Human chr19 + 10666836 10666836 10666836 GAACATAGTGAAACCCTGTCCCTACTAAAAATACAAAAATTCGCCGGGTGTGGCGACACACACCT GAACATAGTGAAACCCTGTCCCTACTAAAAATGCAAAAATTCGCCGGGTGTGGCGACACACACCT A G ILF3 Ensembl:ENSG00000129351 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1328546487 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25381517 24360 RMVar_ID_24360 Human_SNP_ID_658267659 A-to-I Human chr19 + 10667028 10667028 10667028 ACAAAAAGTGTTGGCTTTGCATCGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGACTGAACT ACAAAAAGTGTTGGCTTTGCATCGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGACTGAACT A G ILF3 Ensembl:ENSG00000129351 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1236597644 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13359254 24361 RMVar_ID_24361 Human_SNP_ID_658268362 A-to-I Human chr19 + 10669020 10669020 10669020 ACTCTATTTGCCACGCAGGAGTGCAGTGGCGCAATCTCAGCTCACTGCAACCTCTGCCTCCCGGT ACTCTATTTGCCACGCAGGAGTGCAGTGGCGCGATCTCAGCTCACTGCAACCTCTGCCTCCCGGT A G ILF3 Ensembl:ENSG00000129351 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1000966910 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13359347 24362 RMVar_ID_24362 Human_SNP_ID_658268416 A-to-I Human chr19 + 10669168 10669168 10669168 GAGAGATGTGGTTTCTCCATGTTAGCCCAGCTAGTCTCTAACTCCTGACCTCAAGTGATCCACCC GAGAGATGTGGTTTCTCCATGTTAGCCCAGCTGGTCTCTAACTCCTGACCTCAAGTGATCCACCC A G ILF3 Ensembl:ENSG00000129351 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1368777770 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13359352 24363 RMVar_ID_24363 Human_SNP_ID_658283752 A-to-I Human chr19 + 10715007 10715003 10715007 ATGGAAAAAGTAGGCCAGGTGCAGTGGCTCACACCTGTAATCCCAGCTACTCTGGAGGCTGAGGC ATGGAAAAAGTAGGCCAGGTGCAGTGGCACGTGCCTGTAATCCCAGCTACTCTGGAGGCTGAGGC TCACA ACGTG lnc-TIMM29-1 RNACentral:URS00009B4C85 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1568255206 Functional Loss MNV dbSNP153 29..33 33 - - - 24364 RMVar_ID_24364 Human_SNP_ID_658284005 A-to-I Human chr19 + 10715634 10715634 10715634 GGTGGCAGGCGCCTGTAGTCCCAGCTACTTGAAAGGCTGAGGCAGGAGAATCATTTGAACCCGGG GGTGGCAGGCGCCTGTAGTCCCAGCTACTTGACAGGCTGAGGCAGGAGAATCATTTGAACCCGGG A C lnc-TIMM29-1 RNACentral:URS00009B4C85 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1383961027 Functional Loss SNV dbSNP153 33..33 33 - - - 24365 RMVar_ID_24365 Human_SNP_ID_658285952 A-to-I Human chr19 + 10722753 10722753 10722753 GCTCAAGCGATTCTCCTACCTCTCAGCCTCCTAAGTAGCTGGGACTACAGGCACGTGCCACCACG GCTCAAGCGATTCTCCTACCTCTCAGCCTCCTCAGTAGCTGGGACTACAGGCACGTGCCACCACG A C DNM2 Ensembl:ENSG00000079805 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs922007849 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105373,RMVar_hsa_circ_192432 24366 RMVar_ID_24366 Human_SNP_ID_658286266 A-to-I Human chr19 + 10723925 10723925 10723925 ACCAGCCTGGGCAACATAGACCCCGTCTCTACAAAAAATAAAAACATTAGCTGGGCATGGTGACA ACCAGCCTGGGCAACATAGACCCCGTCTCTACTAAAAATAAAAACATTAGCTGGGCATGGTGACA A T DNM2 Ensembl:ENSG00000079805 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985697893 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105373,RMVar_hsa_circ_192432 24367 RMVar_ID_24367 Human_SNP_ID_658286267 A-to-I Human chr19 + 10723932 10723931 10723932 TGGGCAACATAGACCCCGTCTCTACAAAAAATAAAAACATTAGCTGGGCATGGTGACACCTGTAG TGGGCAACATAGACCCCGTCTCTACAAAAAAT_AAAACATTAGCTGGGCATGGTGACACCTGTAG TA T DNM2 Ensembl:ENSG00000079805 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1169092312 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_105373,RMVar_hsa_circ_192432 24368 RMVar_ID_24368 Human_SNP_ID_658286277 A-to-I Human chr19 + 10723973 10723973 10723973 AGCTGGGCATGGTGACACCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCCGGAGGATGGCTTGAG AGCTGGGCATGGTGACACCTGTAGTCCCAGCTGCTCAGGAGGCTGAGGCCGGAGGATGGCTTGAG A G DNM2 Ensembl:ENSG00000079805 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1426680453 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105373,RMVar_hsa_circ_192432 24369 RMVar_ID_24369 Human_SNP_ID_658288020 A-to-I Human chr19 + 10730129 10730129 10730129 CATGCGATCCTTTCACGTTGGCCCCCCAAAGTACTGGGATTGTAGACATGAGCCACCTCTCCCAG CATGCGATCCTTTCACGTTGGCCCCCCAAAGTTCTGGGATTGTAGACATGAGCCACCTCTCCCAG A T DNM2 Ensembl:ENSG00000079805 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1390678683 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17567559 RMVar_hsa_circ_105373,RMVar_hsa_circ_192432 24370 RMVar_ID_24370 Human_SNP_ID_658292562 A-to-I Human chr19 + 10746479 10746479 10746479 GAGTTTCACTCTTATTGCCCAGGCAGGAGTGTAATGGTGTGATCTTGGCTGACTGTAACCTCTGC GAGTTTCACTCTTATTGCCCAGGCAGGAGTGTGATGGTGTGATCTTGGCTGACTGTAACCTCTGC A G DNM2 Ensembl:ENSG00000079805 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs907814462 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105373,RMVar_hsa_circ_192432 24371 RMVar_ID_24371 Human_SNP_ID_658298338 A-to-I Human chr19 + 10767826 10767826 10767826 TACTTGGGAGGCCGAAGTATGAGAATAGCTTGAACCGGGGAGGCAGAGGTTGCAGTGAGCCGAGA TACTTGGGAGGCCGAAGTATGAGAATAGCTTGGACCGGGGAGGCAGAGGTTGCAGTGAGCCGAGA A G DNM2 Ensembl:ENSG00000079805 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1354597044 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36659,RMVar_hsa_circ_318285,RMVar_hsa_circ_371966,RMVar_hsa_circ_328562,RMVar_hsa_circ_109643,RMVar_hsa_circ_192433,RMVar_hsa_circ_192435,RMVar_hsa_circ_192436,RMVar_hsa_circ_192434 24372 RMVar_ID_24372 Human_SNP_ID_658300912 A-to-I Human chr19 + 10777664 10777664 10777664 TCACCCAAGCTATAGTACAGTGGCACAATCTCAGCTCACTGCAACCTCCGCCTCCCAGGTTCAAC TCACCCAAGCTATAGTACAGTGGCACAATCTCGGCTCACTGCAACCTCCGCCTCCCAGGTTCAAC A G DNM2 Ensembl:ENSG00000079805 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs186884513 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_90,Clinvar_Rec_91 RMVar_hsa_circ_27757,RMVar_hsa_circ_36659,RMVar_hsa_circ_318285,RMVar_hsa_circ_109643,RMVar_hsa_circ_192435,RMVar_hsa_circ_192436,RMVar_hsa_circ_274416,RMVar_hsa_circ_307512,RMVar_hsa_circ_368856,RMVar_hsa_circ_29059,RMVar_hsa_circ_124037,RMVar_hsa_circ_192438,RMVar_hsa_circ_26942,RMVar_hsa_circ_192437,RMVar_hsa_circ_192441,RMVar_hsa_circ_192442,RMVar_hsa_circ_125419 24373 RMVar_ID_24373 Human_SNP_ID_658301126 A-to-I Human chr19 + 10778505 10778505 10778505 AAGTCCCTGTCTCTACTAAAGATTAAAAAGTTAGCTGGGCATGGTGGCATACACCTATAGTCCCA AAGTCCCTGTCTCTACTAAAGATTAAAAAGTTGGCTGGGCATGGTGGCATACACCTATAGTCCCA A G DNM2 Ensembl:ENSG00000079805 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1279086201 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27757,RMVar_hsa_circ_36659,RMVar_hsa_circ_318285,RMVar_hsa_circ_109643,RMVar_hsa_circ_192435,RMVar_hsa_circ_192436,RMVar_hsa_circ_274416,RMVar_hsa_circ_307512,RMVar_hsa_circ_368856,RMVar_hsa_circ_29059,RMVar_hsa_circ_124037,RMVar_hsa_circ_192438,RMVar_hsa_circ_26942,RMVar_hsa_circ_192437,RMVar_hsa_circ_192441,RMVar_hsa_circ_192442,RMVar_hsa_circ_125419 24374 RMVar_ID_24374 Human_SNP_ID_658301132 A-to-I Human chr19 + 10778529 10778529 10778529 AAAAAGTTAGCTGGGCATGGTGGCATACACCTATAGTCCCACCTACTTAAGAGGCTGAGGTGGGA AAAAAGTTAGCTGGGCATGGTGGCATACACCTGTAGTCCCACCTACTTAAGAGGCTGAGGTGGGA A G DNM2 Ensembl:ENSG00000079805 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs768309155 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27757,RMVar_hsa_circ_36659,RMVar_hsa_circ_318285,RMVar_hsa_circ_109643,RMVar_hsa_circ_192435,RMVar_hsa_circ_192436,RMVar_hsa_circ_274416,RMVar_hsa_circ_307512,RMVar_hsa_circ_368856,RMVar_hsa_circ_29059,RMVar_hsa_circ_124037,RMVar_hsa_circ_192438,RMVar_hsa_circ_26942,RMVar_hsa_circ_192437,RMVar_hsa_circ_192441,RMVar_hsa_circ_192442,RMVar_hsa_circ_125419 24375 RMVar_ID_24375 Human_SNP_ID_658301976 A-to-I Human chr19 + 10781634 10781634 10781634 GAAACCCCGTCTCTACTAAAAAAACAAAAATTAGCCAGGCGTGGTGACGCACGCCTGTAATCCCA GAAACCCCGTCTCTACTAAAAAAACAAAAATTGGCCAGGCGTGGTGACGCACGCCTGTAATCCCA A G DNM2 Ensembl:ENSG00000079805 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1254298567 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27757,RMVar_hsa_circ_36659,RMVar_hsa_circ_318285,RMVar_hsa_circ_109643,RMVar_hsa_circ_192435,RMVar_hsa_circ_192436,RMVar_hsa_circ_274416,RMVar_hsa_circ_307512,RMVar_hsa_circ_368856,RMVar_hsa_circ_29059,RMVar_hsa_circ_124037,RMVar_hsa_circ_192438,RMVar_hsa_circ_26942,RMVar_hsa_circ_192437,RMVar_hsa_circ_192441,RMVar_hsa_circ_192442,RMVar_hsa_circ_125419 24376 RMVar_ID_24376 Human_SNP_ID_658301993 A-to-I Human chr19 + 10781706 10781706 10781706 AGGAGGTGGAGGTTGCAGTGAGCTGAGGTTGCACCACTGCACTTCAGCCTGGGCAGCAAGAGTGA AGGAGGTGGAGGTTGCAGTGAGCTGAGGTTGCCCCACTGCACTTCAGCCTGGGCAGCAAGAGTGA A C DNM2 Ensembl:ENSG00000079805 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1475079464 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1956445 RMVar_hsa_circ_27757,RMVar_hsa_circ_36659,RMVar_hsa_circ_318285,RMVar_hsa_circ_109643,RMVar_hsa_circ_192435,RMVar_hsa_circ_192436,RMVar_hsa_circ_274416,RMVar_hsa_circ_307512,RMVar_hsa_circ_368856,RMVar_hsa_circ_29059,RMVar_hsa_circ_124037,RMVar_hsa_circ_192438,RMVar_hsa_circ_26942,RMVar_hsa_circ_192437,RMVar_hsa_circ_192441,RMVar_hsa_circ_192442,RMVar_hsa_circ_125419 24377 RMVar_ID_24377 Human_SNP_ID_658305518 A-to-I Human chr19 + 10794577 10794577 10794577 CAGCCTGGGCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTATCCAGGTGTGGTGG CAGCCTGGGCAACATGGTGAAACCCCATCTCTGCTAAAAATACAAAAATTATCCAGGTGTGGTGG A G DNM2 Ensembl:ENSG00000079805 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1480572064 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_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_27079,RMVar_hsa_circ_192443,RMVar_hsa_circ_192444,RMVar_hsa_circ_51476 24378 RMVar_ID_24378 Human_SNP_ID_658306950 A-to-I Human chr19 + 10799627 10799627 10799627 ACGATCTTGACTCACTGCCACCTCCACTTCCCAGGTTCAAGTGATTCTCATGCCTCAGCCTCCGA ACGATCTTGACTCACTGCCACCTCCACTTCCCGGGTTCAAGTGATTCTCATGCCTCAGCCTCCGA A G DNM2 Ensembl:ENSG00000079805 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1259806209 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_318285,RMVar_hsa_circ_109643,RMVar_hsa_circ_192435,RMVar_hsa_circ_192436,RMVar_hsa_circ_368856,RMVar_hsa_circ_10050,RMVar_hsa_circ_124037,RMVar_hsa_circ_26942,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_51476,RMVar_hsa_circ_352475,RMVar_hsa_circ_358374,RMVar_hsa_circ_300165,RMVar_hsa_circ_192446,RMVar_hsa_circ_76541,RMVar_hsa_circ_192448,RMVar_hsa_circ_14402,RMVar_hsa_circ_286239,RMVar_hsa_circ_192449 24379 RMVar_ID_24379 Human_SNP_ID_658306971 A-to-I Human chr19 + 10799734 10799734 10799734 TTTTGTATTTTTAGTAGAGAGAGATTTTCACTATGTTGGCCAGGCTGGTCTTGAACTCCTGACCT TTTTGTATTTTTAGTAGAGAGAGATTTTCACTCTGTTGGCCAGGCTGGTCTTGAACTCCTGACCT A C DNM2 Ensembl:ENSG00000079805 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1396023856 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_318285,RMVar_hsa_circ_109643,RMVar_hsa_circ_192435,RMVar_hsa_circ_192436,RMVar_hsa_circ_368856,RMVar_hsa_circ_10050,RMVar_hsa_circ_124037,RMVar_hsa_circ_26942,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_51476,RMVar_hsa_circ_352475,RMVar_hsa_circ_358374,RMVar_hsa_circ_300165,RMVar_hsa_circ_192446,RMVar_hsa_circ_76541,RMVar_hsa_circ_192448,RMVar_hsa_circ_14402,RMVar_hsa_circ_286239,RMVar_hsa_circ_192449 24380 RMVar_ID_24380 Human_SNP_ID_658308658 A-to-I Human chr19 + 10806549 10806549 10806549 ACGATAGCTCACACCTGTAATTCTAGCATGTTAGGAGGCTGAGGCGGGCGGATTGCCTGAGCTCA ACGATAGCTCACACCTGTAATTCTAGCATGTTGGGAGGCTGAGGCGGGCGGATTGCCTGAGCTCA A G DNM2 Ensembl:ENSG00000079805 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1344927769 Functional Loss SNV dbSNP153 33..33 33 - - - 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 24381 RMVar_ID_24381 Human_SNP_ID_658308811 A-to-I Human chr19 + 10807147 10807147 10807147 TGGGCTGCAGTGCAGTGGCGCAATCTTGGCTCACTGCAACCTCTGCCTCCCAGGTTCAAGCGATT TGGGCTGCAGTGCAGTGGCGCAATCTTGGCTCGCTGCAACCTCTGCCTCCCAGGTTCAAGCGATT A G DNM2 Ensembl:ENSG00000079805 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1198294257 Functional Loss SNV dbSNP153 33..33 33 - - - 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 24382 RMVar_ID_24382 Human_SNP_ID_658308813 A-to-I Human chr19 + 10807152 10807152 10807152 TGCAGTGCAGTGGCGCAATCTTGGCTCACTGCAACCTCTGCCTCCCAGGTTCAAGCGATTCTCCT TGCAGTGCAGTGGCGCAATCTTGGCTCACTGCTACCTCTGCCTCCCAGGTTCAAGCGATTCTCCT A T DNM2 Ensembl:ENSG00000079805 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1011982666 Functional Loss SNV dbSNP153 33..33 33 - - - 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 24383 RMVar_ID_24383 Human_SNP_ID_658308867 A-to-I Human chr19 + 10807357 10807357 10807357 CCACCTCCCGGGTTCAAGCAATTCTCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCGCCCG CCACCTCCCGGGTTCAAGCAATTCTCTGCCTCGGCCTCCTGAGTAGCTGGGATTACAGGCGCCCG A G DNM2 Ensembl:ENSG00000079805 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs964746422 Functional Loss SNV dbSNP153 33..33 33 - - - 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 24384 RMVar_ID_24384 Human_SNP_ID_658308885 A-to-I Human chr19 + 10807401 10807401 10807401 AGCTGGGATTACAGGCGCCCGCCAGCACGCCCAGCTAATTTTTTTGTATTTTTAGTAGAGAGGGG AGCTGGGATTACAGGCGCCCGCCAGCACGCCCGGCTAATTTTTTTGTATTTTTAGTAGAGAGGGG A G DNM2 Ensembl:ENSG00000079805 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1222437142 Functional Loss SNV dbSNP153 33..33 33 - - - 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 24385 RMVar_ID_24385 Human_SNP_ID_658308966 A-to-I Human chr19 + 10807618 10807618 10807618 CCACCAAGGCTGGAGTGCAGTGGCGCGGTCTCAGCTCACCACAACCTCCGCCTCCTAGCTTCGTG CCACCAAGGCTGGAGTGCAGTGGCGCGGTCTCGGCTCACCACAACCTCCGCCTCCTAGCTTCGTG A G DNM2 Ensembl:ENSG00000079805 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs983201733 Functional Loss SNV dbSNP153 33..33 33 - - - 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 24386 RMVar_ID_24386 Human_SNP_ID_658308991 A-to-I Human chr19 + 10807688 10807688 10807688 CTCCTGCCTCAGCCTTCTGAGTAGCGACGATTACAGGAGCCTGCCACCACCCCTGACTAATTTCT CTCCTGCCTCAGCCTTCTGAGTAGCGACGATTGCAGGAGCCTGCCACCACCCCTGACTAATTTCT A G DNM2 Ensembl:ENSG00000079805 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1295759957 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13361787 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 24387 RMVar_ID_24387 Human_SNP_ID_658309071 A-to-I Human chr19 + 10808020 10808020 10808020 AAAAAATTAGCCTGGCATGATGGTGGGTGCCTATAATTCCACCTACTCGGGAGGTTGAGACAGGA AAAAAATTAGCCTGGCATGATGGTGGGTGCCTGTAATTCCACCTACTCGGGAGGTTGAGACAGGA A G DNM2 Ensembl:ENSG00000079805 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1023551512 Functional Loss SNV dbSNP153 33..33 33 - - - 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 24388 RMVar_ID_24388 Human_SNP_ID_658309081 A-to-I Human chr19 + 10808068 10808068 10808068 GGGAGGTTGAGACAGGAGAATCACTTGAACCCAGGAGATGGTGGTTGTGGTGAGCCAGGATCACA GGGAGGTTGAGACAGGAGAATCACTTGAACCCGGGAGATGGTGGTTGTGGTGAGCCAGGATCACA A G DNM2 Ensembl:ENSG00000079805 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1377241637 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17567582 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 24389 RMVar_ID_24389 Human_SNP_ID_658309083 A-to-I Human chr19 + 10808092 10808092 10808092 TTGAACCCAGGAGATGGTGGTTGTGGTGAGCCAGGATCACACCACTGCACTCTGGCCTGGGCGGC TTGAACCCAGGAGATGGTGGTTGTGGTGAGCCGGGATCACACCACTGCACTCTGGCCTGGGCGGC A G DNM2 Ensembl:ENSG00000079805 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs915340983 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17567582,Human_RBP_ID_23309187 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 24390 RMVar_ID_24390 Human_SNP_ID_658312955 A-to-I Human chr19 + 10822289 10822289 10822289 TCAGCTCATTGTAGCCTCCACCTCCCATGCTCAAGTGATCCTCCCGCCTCGGCCTCCCGAGTAGC TCAGCTCATTGTAGCCTCCACCTCCCATGCTCCAGTGATCCTCCCGCCTCGGCCTCCCGAGTAGC A C DNM2 Ensembl:ENSG00000079805 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917308710 Functional Loss SNV dbSNP153 33..33 33 - - - 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_107615,RMVar_hsa_circ_26526,RMVar_hsa_circ_192454,RMVar_hsa_circ_88745,RMVar_hsa_circ_339417 24391 RMVar_ID_24391 Human_SNP_ID_658330393 A-to-I Human chr19 + 10880554 10880554 10880554 TTTTTTTTTTTTTGTAGAGACAGGGTCTCACTATGTTGCTCAGGCGGATGTGGAACTCCTGGGCT TTTTTTTTTTTTTGTAGAGACAGGGTCTCACTGTGTTGCTCAGGCGGATGTGGAACTCCTGGGCT A G CARM1 Ensembl:ENSG00000142453 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1040721038 Functional Loss SNV dbSNP153 33..33 33 - - - 24392 RMVar_ID_24392 Human_SNP_ID_658330413 A-to-I Human chr19 + 10880601 10880601 10880601 ATGTGGAACTCCTGGGCTCAAGCGATTCTCCTACCTTGGCCCCCAAAGTGCTGGGATTACAGGTG ATGTGGAACTCCTGGGCTCAAGCGATTCTCCTCCCTTGGCCCCCAAAGTGCTGGGATTACAGGTG A C CARM1 Ensembl:ENSG00000142453 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs562619460 Functional Loss SNV dbSNP153 33..33 33 - - - 24393 RMVar_ID_24393 Human_SNP_ID_658330414 A-to-I Human chr19 + 10880601 10880601 10880601 ATGTGGAACTCCTGGGCTCAAGCGATTCTCCTACCTTGGCCCCCAAAGTGCTGGGATTACAGGTG ATGTGGAACTCCTGGGCTCAAGCGATTCTCCTGCCTTGGCCCCCAAAGTGCTGGGATTACAGGTG A G CARM1 Ensembl:ENSG00000142453 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs562619460 Functional Loss SNV dbSNP153 33..33 33 - - - 24394 RMVar_ID_24394 Human_SNP_ID_658331473 A-to-I Human chr19 + 10884296 10884285 10884297 CCAGGAGATGGAGGTTGTGGTGACCACAGATCACACAACTGCACTCCAGCCTGGTCAACAAGAGC CCAGGAGATGGAGGTTGTGGTG____________ACAACTGCACTCCAGCCTGGTCAACAAGAGC GACCACAGATCAC G CARM1 Ensembl:ENSG00000142453 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1279467511 Functional Loss DEL dbSNP153 23..34 33 - - - 24395 RMVar_ID_24395 Human_SNP_ID_658331648 A-to-I Human chr19 + 10884870 10884870 10884870 GGGATCATAGACACGTGCCACCACGCCTGCCTAATTTTTGGATTTTTAGTAGAGACGGGGTTTCA GGGATCATAGACACGTGCCACCACGCCTGCCTCATTTTTGGATTTTTAGTAGAGACGGGGTTTCA A C CARM1 Ensembl:ENSG00000142453 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1218455430 Functional Loss SNV dbSNP153 33..33 33 - - - 24396 RMVar_ID_24396 Human_SNP_ID_658340594 A-to-I Human chr19 + 10917262 10917262 10917262 TAATCCCAGCACTTTGGGAGGCCAAGGCGGGCAGATCACGAGGTTAGGAGATTGAGACCAACACG TAATCCCAGCACTTTGGGAGGCCAAGGCGGGCTGATCACGAGGTTAGGAGATTGAGACCAACACG A T CARM1 Ensembl:ENSG00000142453 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1004934874 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10779,RMVar_hsa_circ_347974,RMVar_hsa_circ_80372,RMVar_hsa_circ_192456,RMVar_hsa_circ_192457,RMVar_hsa_circ_192467,RMVar_hsa_circ_123865 24397 RMVar_ID_24397 Human_SNP_ID_658345069 A-to-I Human chr19 + 10930148 10930148 10930148 TGCAAACTGAGGCAAGAGAATCGCTTGAGGCCAGGAGTTTGAGGCCAGCTAGAGTGACATAGCAA TGCAAACTGAGGCAAGAGAATCGCTTGAGGCCGGGAGTTTGAGGCCAGCTAGAGTGACATAGCAA A G TIMM29 Ensembl:ENSG00000142444 Protein coding 3'UTR GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs538038079 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23781438 24398 RMVar_ID_24398 Human_SNP_ID_658345194 A-to-I Human chr19 + 10930534 10930534 10930534 GACCTCAGGTGATCCACCTGCCTCGCATTTCCAAAGTGCTGGGATTATAGGAGTGAACCACCACA GACCTCAGGTGATCCACCTGCCTCGCATTTCCGAAGTGCTGGGATTATAGGAGTGAACCACCACA A G TIMM29 Ensembl:ENSG00000142444 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1217675934 Functional Loss SNV dbSNP153 33..33 33 - - - 24399 RMVar_ID_24399 Human_SNP_ID_658345217 A-to-I Human chr19 + 10930618 10930618 10930618 AAGTAACATTTTTGCCATTCCCAGCTCTTTGGAAGGCTGAGGTAGGAGGATTGCTTGAGATCAGG AAGTAACATTTTTGCCATTCCCAGCTCTTTGGGAGGCTGAGGTAGGAGGATTGCTTGAGATCAGG A G TIMM29 Ensembl:ENSG00000142444 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1263413167 Functional Loss SNV dbSNP153 33..33 33 - - - 24400 RMVar_ID_24400 Human_SNP_ID_658345308 A-to-I Human chr19 + 10930978 10930978 10930978 CCACGATCGTGCCACTGCACTCCATCTTGGACAACAGAGTGAGACTGTCTCAAAAAGTAAAATAA CCACGATCGTGCCACTGCACTCCATCTTGGACCACAGAGTGAGACTGTCTCAAAAAGTAAAATAA A C TIMM29 Ensembl:ENSG00000142444 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1024229382 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13363052 24401 RMVar_ID_24401 Human_SNP_ID_658345309 A-to-I Human chr19 + 10930981 10930981 10930981 CGATCGTGCCACTGCACTCCATCTTGGACAACAGAGTGAGACTGTCTCAAAAAGTAAAATAAGTG CGATCGTGCCACTGCACTCCATCTTGGACAACGGAGTGAGACTGTCTCAAAAAGTAAAATAAGTG A G TIMM29 Ensembl:ENSG00000142444 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1267580193 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13363052 24402 RMVar_ID_24402 Human_SNP_ID_658345397 A-to-I Human chr19 + 10931266 10931266 10931266 CCTGGCTAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTACCGGGGCGTGGTGGCG CCTGGCTAACATGGTGAAACCCCGTCTCTACTGAAAATACAAAAAATTACCGGGGCGTGGTGGCG A G TIMM29 Ensembl:ENSG00000142444 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1449058471 Functional Loss SNV dbSNP153 33..33 33 - - - 24403 RMVar_ID_24403 Human_SNP_ID_658345554 A-to-I Human chr19 + 10931659 10931658 10931660 TGTTTTGATTTTTTTAAGTTTTTTTTTGAGACAGAGTTTCGCTCTTGTTGCCCAGGCTGGAGTGC TGTTTTGATTTTTTTAAGTTTTTTTTTGAGAC__AGTTTCGCTCTTGTTGCCCAGGCTGGAGTGC CAG C TIMM29 Ensembl:ENSG00000142444 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1315634730 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_13363054 24404 RMVar_ID_24404 Human_SNP_ID_658345622 A-to-I Human chr19 + 10931890 10931890 10931890 ACCTCAGGTGATCCGCCTGCCTCAGCCTCCCAAAGTGCTGGGATTGCAGACGTGAGCCACCGTGC ACCTCAGGTGATCCGCCTGCCTCAGCCTCCCAGAGTGCTGGGATTGCAGACGTGAGCCACCGTGC A G TIMM29 Ensembl:ENSG00000142444 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1282123736 Functional Loss SNV dbSNP153 33..33 33 - - - 24405 RMVar_ID_24405 Human_SNP_ID_658345706 A-to-I Human chr19 + 10932233 10932232 10932234 TGTATTTTTGTTGTTGTTGTTGTTGTTGAGACAGAGTCTCACTCTGACACCCAGGCTGGAGTGCA TGTATTTTTGTTGTTGTTGTTGTTGTTGAGAC__AGTCTCACTCTGACACCCAGGCTGGAGTGCA CAG C TIMM29 Ensembl:ENSG00000142444 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1332066504 Functional Loss DEL dbSNP153 33..34 33 - - - Human_Splice_Rec_1956863 24406 RMVar_ID_24406 Human_SNP_ID_658345931 A-to-I Human chr19 + 10933036 10933036 10933036 GGTATGGTACACACCTGTACTACCAACTATTCAGGAGGCTGAGGTGGAAGAATTGCTTGAGCTTG GGTATGGTACACACCTGTACTACCAACTATTCGGGAGGCTGAGGTGGAAGAATTGCTTGAGCTTG A G TIMM29 Ensembl:ENSG00000142444 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs570416399 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1371843,Human_RBP_ID_2555754,Human_RBP_ID_13363068 24407 RMVar_ID_24407 Human_SNP_ID_658345963 A-to-I Human chr19 + 10933187 10933187 10933187 GGCTGGATGCGGTGGCTCACGCATGTGATCCCAGCACTTTGGGAGGCTGAGGTGGGTGGATCACA GGCTGGATGCGGTGGCTCACGCATGTGATCCCGGCACTTTGGGAGGCTGAGGTGGGTGGATCACA A G TIMM29 Ensembl:ENSG00000142444 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1237918836 Functional Loss SNV dbSNP153 33..33 33 - - - 24408 RMVar_ID_24408 Human_SNP_ID_658354750 A-to-I Human chr19 + 10962811 10962811 10962811 GTGATCCACCCACCTCGGCCTCCCAAAGTGCTAGGACTACATGTGTGAGCCACTGCGCCAGGATT GTGATCCACCCACCTCGGCCTCCCAAAGTGCTGGGACTACATGTGTGAGCCACTGCGCCAGGATT A G SMARCA4 Ensembl:ENSG00000127616 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1395165294 Functional Loss SNV dbSNP153 33..33 33 - - - 24409 RMVar_ID_24409 Human_SNP_ID_658355714 A-to-I Human chr19 + 10966258 10966258 10966258 CACCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGACGTGAGCTACCGCGCCCGGCCAGGTTTT CACCTGCCTCAGCCTCCCAAAGTGCTGGGATTGCAGACGTGAGCTACCGCGCCCGGCCAGGTTTT A G SMARCA4 Ensembl:ENSG00000127616 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1458958809 Functional Loss SNV dbSNP153 33..33 33 - - - 24410 RMVar_ID_24410 Human_SNP_ID_658355841 A-to-I Human chr19 + 10966749 10966749 10966749 CTCTACGAAAATACAAAAGAAATTAGCTGGGCATGGTGGTGTGCGCCTGTAGTCCTAGCTACTTG CTCTACGAAAATACAAAAGAAATTAGCTGGGCGTGGTGGTGTGCGCCTGTAGTCCTAGCTACTTG A G SMARCA4 Ensembl:ENSG00000127616 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1044727271 Functional Loss SNV dbSNP153 33..33 33 - - - 24411 RMVar_ID_24411 Human_SNP_ID_658358736 A-to-I Human chr19 + 10976620 10976620 10976620 TCTATAAAGAAATACAAAAATTAGCTGGGCATAGTGGCATGAGCCTGTAGTCCCAGCTACTCGGG TCTATAAAGAAATACAAAAATTAGCTGGGCATGGTGGCATGAGCCTGTAGTCCCAGCTACTCGGG A G SMARCA4 Ensembl:ENSG00000127616 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1274449846 Functional Loss SNV dbSNP153 33..33 33 - - - 24412 RMVar_ID_24412 Human_SNP_ID_658365206 A-to-I Human chr19 + 10997600 10997600 10997600 CACCCGCCTTGGCCTCCCAAAGTGCCAGGATTACAGGCATAAGCCACCACGCCTGGCCTAATTTT CACCCGCCTTGGCCTCCCAAAGTGCCAGGATTGCAGGCATAAGCCACCACGCCTGGCCTAATTTT A G SMARCA4 Ensembl:ENSG00000127616 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1384795484 Functional Loss SNV dbSNP153 33..33 33 - - - 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_192482 24413 RMVar_ID_24413 Human_SNP_ID_658365691 A-to-I Human chr19 + 10999437 10999437 10999437 CCAGTACTTTGGGAGGCCAATATGGGAGGACTACTTGAGCCCAGGAGTTCGAGACCAGTGTGGGC CCAGTACTTTGGGAGGCCAATATGGGAGGACTCCTTGAGCCCAGGAGTTCGAGACCAGTGTGGGC A C SMARCA4 Ensembl:ENSG00000127616 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs927199878 Functional Loss SNV dbSNP153 33..33 33 - - - 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_192482 24414 RMVar_ID_24414 Human_SNP_ID_658365692 A-to-I Human chr19 + 10999437 10999437 10999437 CCAGTACTTTGGGAGGCCAATATGGGAGGACTACTTGAGCCCAGGAGTTCGAGACCAGTGTGGGC CCAGTACTTTGGGAGGCCAATATGGGAGGACTGCTTGAGCCCAGGAGTTCGAGACCAGTGTGGGC A G SMARCA4 Ensembl:ENSG00000127616 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs927199878 Functional Loss SNV dbSNP153 33..33 33 - - - 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_192482 24415 RMVar_ID_24415 Human_SNP_ID_658365931 A-to-I Human chr19 + 11000407 11000407 11000407 AAAAATTAACCAGGCTTGGTGCGCACGCCTGTAGTCCCACCTACTCGAGAGGCTGAGGTAGGGGG AAAAATTAACCAGGCTTGGTGCGCACGCCTGTGGTCCCACCTACTCGAGAGGCTGAGGTAGGGGG A G SMARCA4 Ensembl:ENSG00000127616 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs79351488 Functional Loss SNV dbSNP153 33..33 33 - - - 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_192482 24416 RMVar_ID_24416 Human_SNP_ID_658367597 A-to-I Human chr19 + 11006570 11006570 11006570 GTCAGGAGTTCGAGACCAGCCTGGCCAACATGATGAAACCCCGTCTCTACTAAAAAATACAAAAA GTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAAATACAAAAA A G SMARCA4 Ensembl:ENSG00000127616 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs147318343 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_92 GWAS_ID_2330,GWAS_ID_2331,GWAS_ID_2332,GWAS_ID_2333,GWAS_ID_2334,GWAS_ID_2335,GWAS_ID_2336,GWAS_ID_2337,GWAS_ID_2338,GWAS_ID_2339 RMVar_hsa_circ_2241,RMVar_hsa_circ_39568,RMVar_hsa_circ_51477,RMVar_hsa_circ_332540,RMVar_hsa_circ_7395,RMVar_hsa_circ_5044,RMVar_hsa_circ_75898,RMVar_hsa_circ_192482,RMVar_hsa_circ_21252,RMVar_hsa_circ_114765,RMVar_hsa_circ_192484 24417 RMVar_ID_24417 Human_SNP_ID_658368227 A-to-I Human chr19 + 11008863 11008863 11008863 GGGCGTGGTGGCGTGCACCTGGAGTCCCAGCTACTTGGGAGGCTGAGACAGGAGAATCGCTTGAA GGGCGTGGTGGCGTGCACCTGGAGTCCCAGCTGCTTGGGAGGCTGAGACAGGAGAATCGCTTGAA A G SMARCA4 Ensembl:ENSG00000127616 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs976069730 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39568,RMVar_hsa_circ_51477,RMVar_hsa_circ_332540,RMVar_hsa_circ_7395,RMVar_hsa_circ_5044,RMVar_hsa_circ_75898,RMVar_hsa_circ_192482,RMVar_hsa_circ_21252,RMVar_hsa_circ_114765,RMVar_hsa_circ_307638,RMVar_hsa_circ_192484,RMVar_hsa_circ_288254,RMVar_hsa_circ_192486,RMVar_hsa_circ_192487 24418 RMVar_ID_24418 Human_SNP_ID_658369240 A-to-I Human chr19 + 11012319 11012310 11012319 TTGAACCTGGGAGGCAGAGGTTGCAGTGAGCCAAGATCGGGCCACTGCACTCCAGCTTGGGTGAG TTGAACCTGGGAGGCAGAGGTTGC_________AGATCGGGCCACTGCACTCCAGCTTGGGTGAG CAGTGAGCCA C SMARCA4 Ensembl:ENSG00000127616 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1161734673 Functional Loss DEL dbSNP153 25..33 33 - - - RMVar_hsa_circ_39568,RMVar_hsa_circ_51477,RMVar_hsa_circ_332540,RMVar_hsa_circ_7395,RMVar_hsa_circ_5044,RMVar_hsa_circ_75898,RMVar_hsa_circ_192482,RMVar_hsa_circ_88376,RMVar_hsa_circ_114765,RMVar_hsa_circ_307638,RMVar_hsa_circ_192484,RMVar_hsa_circ_192487,RMVar_hsa_circ_343660,RMVar_hsa_circ_284366,RMVar_hsa_circ_192489,RMVar_hsa_circ_29226,RMVar_hsa_circ_192488 24419 RMVar_ID_24419 Human_SNP_ID_658376241 A-to-I Human chr19 + 11036405 11036405 11036405 CCTCAGCCTCCTGAGTAGTTCAGACTACAGGTACACACCAACACGCCTGGCTAATTTTAAATTTT CCTCAGCCTCCTGAGTAGTTCAGACTACAGGTGCACACCAACACGCCTGGCTAATTTTAAATTTT A G SMARCA4 Ensembl:ENSG00000127616 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1206664303 Functional Loss SNV dbSNP153 33..33 33 - - - 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_14259,RMVar_hsa_circ_325575,RMVar_hsa_circ_82983,RMVar_hsa_circ_192491 24420 RMVar_ID_24420 Human_SNP_ID_658376257 A-to-I Human chr19 + 11036442 11036442 11036442 CCAACACGCCTGGCTAATTTTAAATTTTTTGTAAAGTGGGGGTCTCACTGTGTCACTCAGGCTGG CCAACACGCCTGGCTAATTTTAAATTTTTTGTGAAGTGGGGGTCTCACTGTGTCACTCAGGCTGG A G SMARCA4 Ensembl:ENSG00000127616 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474428060 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13364090 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_14259,RMVar_hsa_circ_325575,RMVar_hsa_circ_82983,RMVar_hsa_circ_192491 24421 RMVar_ID_24421 Human_SNP_ID_658376870 A-to-I Human chr19 + 11038988 11038988 11038988 TGTGCCTGTAATCCCAGCACTTGGAGAAGCCAAAGCGGGGGGATCATTTCAGCTCAGGAGTTTGA TGTGCCTGTAATCCCAGCACTTGGAGAAGCCAGAGCGGGGGGATCATTTCAGCTCAGGAGTTTGA A G SMARCA4 Ensembl:ENSG00000127616 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1269568078 Functional Loss SNV dbSNP153 33..33 33 - - - 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_14259,RMVar_hsa_circ_325575,RMVar_hsa_circ_82983,RMVar_hsa_circ_192491 24422 RMVar_ID_24422 Human_SNP_ID_658377201 A-to-I Human chr19 + 11039960 11039960 11039960 AAAATTAGCTGGACGTGGTGGTGGGCGCCTGTAGTCCCAGCTACTCAGGAGGGTGAGGGAGGAGA AAAATTAGCTGGACGTGGTGGTGGGCGCCTGTGGTCCCAGCTACTCAGGAGGGTGAGGGAGGAGA A G SMARCA4 Ensembl:ENSG00000127616 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1172190297 Functional Loss SNV dbSNP153 33..33 33 - - - 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_14259,RMVar_hsa_circ_325575,RMVar_hsa_circ_82983,RMVar_hsa_circ_192491 24423 RMVar_ID_24423 Human_SNP_ID_658379784 A-to-I Human chr19 + 11048293 11048293 11048293 TCACTCTGTCACCCAGGCTGGAGTGCCATGGCACAATCTCGGCTCCCTGCAACCTCCACCTTCCA TCACTCTGTCACCCAGGCTGGAGTGCCATGGCGCAATCTCGGCTCCCTGCAACCTCCACCTTCCA A G SMARCA4 Ensembl:ENSG00000127616 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs868692552 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75898,RMVar_hsa_circ_192482,RMVar_hsa_circ_88376,RMVar_hsa_circ_192489,RMVar_hsa_circ_8398,RMVar_hsa_circ_192493,RMVar_hsa_circ_276780,RMVar_hsa_circ_11136 24424 RMVar_ID_24424 Human_SNP_ID_658385147 A-to-I Human chr19 + 11065994 11065994 11065994 GTGCCTTAGTCTGGGGGTGTTGGCCCATATCCATAATCCCAGCACTTTGGGAGGCTGAGGCAGGA GTGCCTTAGTCTGGGGGTGTTGGCCCATATCCGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGA A G SMARCA4 Ensembl:ENSG00000127616 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs990601505 Functional Loss SNV dbSNP153 33..33 33 - - - 24425 RMVar_ID_24425 Human_SNP_ID_658393711 A-to-I Human chr19 + 11096144 11096144 11096144 CACCTGTCTCTGCAAAAAATAAATAAAAAGTTAGCTGAGTGTGATGGTGCACCCCTCTAGTCACA CACCTGTCTCTGCAAAAAATAAATAAAAAGTTTGCTGAGTGTGATGGTGCACCCCTCTAGTCACA A T LDLR Ensembl:ENSG00000130164 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1423804181 Functional Loss SNV dbSNP153 33..33 33 - - - 24426 RMVar_ID_24426 Human_SNP_ID_658394016 A-to-I Human chr19 + 11097444 11097444 11097444 GGAGAATCGCTTGAACCTGGGAGGCAGAGGTTACAGTGAGTCAAGATCATACCATTGCACTCCAG GGAGAATCGCTTGAACCTGGGAGGCAGAGGTTGCAGTGAGTCAAGATCATACCATTGCACTCCAG A G LDLR Ensembl:ENSG00000130164 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1427346342 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23310086 24427 RMVar_ID_24427 Human_SNP_ID_658394880 A-to-I Human chr19 + 11100908 11100908 11100908 CCTCAGCCTCCCGAGTAGCTGGGACTACAGGCACCCTCCACCACATCCGGCTAATTTTTTGTATC CCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCCTCCACCACATCCGGCTAATTTTTTGTATC A G LDLR Ensembl:ENSG00000130164 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs753246320 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5611,RMVar_hsa_circ_277209,RMVar_hsa_circ_322490,RMVar_hsa_circ_344045,RMVar_hsa_circ_309511,RMVar_hsa_circ_104770,RMVar_hsa_circ_41213,RMVar_hsa_circ_192499,RMVar_hsa_circ_192500 24428 RMVar_ID_24428 Human_SNP_ID_658395168 A-to-I Human chr19 + 11101899 11101899 11101899 CTTGAGGCCATGAGTTTGAGACCAGCCTGCTCAACATGATGAAACTTCTATCTCTACTAAAAAAA CTTGAGGCCATGAGTTTGAGACCAGCCTGCTCCACATGATGAAACTTCTATCTCTACTAAAAAAA A C LDLR Ensembl:ENSG00000130164 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1303113264 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5611,RMVar_hsa_circ_277209,RMVar_hsa_circ_322490,RMVar_hsa_circ_344045,RMVar_hsa_circ_309511,RMVar_hsa_circ_104770,RMVar_hsa_circ_41213,RMVar_hsa_circ_192499,RMVar_hsa_circ_192500 24429 RMVar_ID_24429 Human_SNP_ID_658395189 A-to-I Human chr19 + 11101964 11101964 11101964 AAAGTGGGATTAGGTCAGGCACGGTGGCTCACACCTGTAATCCCAGCACTTTCAGAGGCCGAGGC AAAGTGGGATTAGGTCAGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTCAGAGGCCGAGGC A G LDLR Ensembl:ENSG00000130164 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs962603426 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5611,RMVar_hsa_circ_277209,RMVar_hsa_circ_322490,RMVar_hsa_circ_344045,RMVar_hsa_circ_309511,RMVar_hsa_circ_104770,RMVar_hsa_circ_41213,RMVar_hsa_circ_192499,RMVar_hsa_circ_192500 24430 RMVar_ID_24430 Human_SNP_ID_658396007 A-to-I Human chr19 + 11104455 11104455 11104455 TAAAATTTCTTTCTTTTTTGAGATGGAGTCTCACTCTGTTTGCCCAGGCTGGAGTTCAGTGGTGC TAAAATTTCTTTCTTTTTTGAGATGGAGTCTCCCTCTGTTTGCCCAGGCTGGAGTTCAGTGGTGC A C LDLR Ensembl:ENSG00000130164 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1007001699 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17567939 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_16496,RMVar_hsa_circ_34618,RMVar_hsa_circ_192500,RMVar_hsa_circ_378050,RMVar_hsa_circ_354925,RMVar_hsa_circ_19308 24431 RMVar_ID_24431 Human_SNP_ID_658396017 A-to-I Human chr19 + 11104494 11104494 11104494 TTGCCCAGGCTGGAGTTCAGTGGTGCAATCTCAGCTCACTGCAACCTCTACCTACTGGGTTCAAG TTGCCCAGGCTGGAGTTCAGTGGTGCAATCTCGGCTCACTGCAACCTCTACCTACTGGGTTCAAG A G LDLR Ensembl:ENSG00000130164 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs995931000 Functional Loss SNV dbSNP153 33..33 33 - - - 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_16496,RMVar_hsa_circ_34618,RMVar_hsa_circ_192500,RMVar_hsa_circ_378050,RMVar_hsa_circ_354925,RMVar_hsa_circ_19308 24432 RMVar_ID_24432 Human_SNP_ID_658396058 A-to-I Human chr19 + 11104658 11104658 11104658 GTTGGCCAAGGTGGTCTTGAACTCCTGACCTCAAGTGATCCTCCCACCTCAGCCTCCCAAAGCGC GTTGGCCAAGGTGGTCTTGAACTCCTGACCTCCAGTGATCCTCCCACCTCAGCCTCCCAAAGCGC A C LDLR Ensembl:ENSG00000130164 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1255581994 Functional Loss SNV dbSNP153 33..33 33 - - - 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_16496,RMVar_hsa_circ_34618,RMVar_hsa_circ_192500,RMVar_hsa_circ_378050,RMVar_hsa_circ_354925,RMVar_hsa_circ_19308 24433 RMVar_ID_24433 Human_SNP_ID_658396075 A-to-I Human chr19 + 11104692 11104692 11104692 GTGATCCTCCCACCTCAGCCTCCCAAAGCGCTAGGATTACGGCCATGAGCCACTGAGGCCGGCTG GTGATCCTCCCACCTCAGCCTCCCAAAGCGCTGGGATTACGGCCATGAGCCACTGAGGCCGGCTG A G LDLR Ensembl:ENSG00000130164 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1472101700 Functional Loss SNV dbSNP153 33..33 33 - - - 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_16496,RMVar_hsa_circ_34618,RMVar_hsa_circ_192500,RMVar_hsa_circ_378050,RMVar_hsa_circ_354925,RMVar_hsa_circ_19308 24434 RMVar_ID_24434 Human_SNP_ID_658398080 A-to-I Human chr19 + 11109910 11109910 11109910 GTAGAGACTGACTGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAAGTGATC GTAGAGACTGACTGGGTTTCACCATGTTGGCCGGGCTGGTCTCGAACTCCTGACCTCAAGTGATC A G LDLR Ensembl:ENSG00000130164 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1214869791 Functional Loss SNV dbSNP153 33..33 33 - - - 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 24435 RMVar_ID_24435 Human_SNP_ID_658400085 A-to-I Human chr19 + 11114864 11114864 11114864 TTGAGACGGAGTCTCGCTCTGTCGCCCAGGCTAGATTGCAGTGGCGTGATCTCGGCTCACTGCAG TTGAGACGGAGTCTCGCTCTGTCGCCCAGGCTGGATTGCAGTGGCGTGATCTCGGCTCACTGCAG A G LDLR Ensembl:ENSG00000130164 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1455352558 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_676,RMVar_hsa_circ_344045,RMVar_hsa_circ_41213,RMVar_hsa_circ_12821,RMVar_hsa_circ_16496,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_23892,RMVar_hsa_circ_51705,RMVar_hsa_circ_321486,RMVar_hsa_circ_62160,RMVar_hsa_circ_48431,RMVar_hsa_circ_89224,RMVar_hsa_circ_192515 24436 RMVar_ID_24436 Human_SNP_ID_658400113 A-to-I Human chr19 + 11114955 11114955 11114955 CTCCTGCCTCAACCTCCCAACTAATTAGGATTACAAGCATGTACCACCATGCCTGACTAATTTTT CTCCTGCCTCAACCTCCCAACTAATTAGGATTGCAAGCATGTACCACCATGCCTGACTAATTTTT A G LDLR Ensembl:ENSG00000130164 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1224164363 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_676,RMVar_hsa_circ_344045,RMVar_hsa_circ_41213,RMVar_hsa_circ_12821,RMVar_hsa_circ_16496,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_23892,RMVar_hsa_circ_51705,RMVar_hsa_circ_321486,RMVar_hsa_circ_62160,RMVar_hsa_circ_48431,RMVar_hsa_circ_89224,RMVar_hsa_circ_192515 24437 RMVar_ID_24437 Human_SNP_ID_658400123 A-to-I Human chr19 + 11115000 11115000 11115000 ACCATGCCTGACTAATTTTTTGTATTTTTAGTAGAGACTGGGTTTCACCATGTTGGCTAGGCTGG ACCATGCCTGACTAATTTTTTGTATTTTTAGTGGAGACTGGGTTTCACCATGTTGGCTAGGCTGG A G LDLR Ensembl:ENSG00000130164 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1253720903 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_676,RMVar_hsa_circ_344045,RMVar_hsa_circ_41213,RMVar_hsa_circ_12821,RMVar_hsa_circ_16496,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_23892,RMVar_hsa_circ_51705,RMVar_hsa_circ_321486,RMVar_hsa_circ_62160,RMVar_hsa_circ_48431,RMVar_hsa_circ_89224,RMVar_hsa_circ_192515 24438 RMVar_ID_24438 Human_SNP_ID_658401621 A-to-I Human chr19 + 11119407 11119407 11119407 GTTGTGGGCCAGGTGTGGTGGTTCATGCCTGTAATCCCAGCACTTTGGGAGGTCAGAGGGAGGTG GTTGTGGGCCAGGTGTGGTGGTTCATGCCTGTGATCCCAGCACTTTGGGAGGTCAGAGGGAGGTG A G LDLR Ensembl:ENSG00000130164 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs963518668 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41213,RMVar_hsa_circ_13639,RMVar_hsa_circ_45258,RMVar_hsa_circ_51705,RMVar_hsa_circ_192519,RMVar_hsa_circ_50951,RMVar_hsa_circ_89224,RMVar_hsa_circ_192515,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_192516,RMVar_hsa_circ_376040,RMVar_hsa_circ_192520 24439 RMVar_ID_24439 Human_SNP_ID_658401718 A-to-I Human chr19 + 11119765 11119765 11119765 GGGAGACCGAGGTAGGTGGATGGCCTGAGGTCAGGAGTTCGAATCCAGCCTGGCCAACATGGTGA GGGAGACCGAGGTAGGTGGATGGCCTGAGGTCGGGAGTTCGAATCCAGCCTGGCCAACATGGTGA A G LDLR Ensembl:ENSG00000130164 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978161190 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41213,RMVar_hsa_circ_13639,RMVar_hsa_circ_45258,RMVar_hsa_circ_51705,RMVar_hsa_circ_192519,RMVar_hsa_circ_50951,RMVar_hsa_circ_89224,RMVar_hsa_circ_192515,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_192516,RMVar_hsa_circ_376040,RMVar_hsa_circ_192520 24440 RMVar_ID_24440 Human_SNP_ID_658403540 A-to-I Human chr19 + 11124255 11124255 11124255 CACCATGCCTGGCTAATTCTTGCATTTTTAGTAGAGATGGGGTTTCACAGTGTTGGCCAGGCTGG CACCATGCCTGGCTAATTCTTGCATTTTTAGTGGAGATGGGGTTTCACAGTGTTGGCCAGGCTGG A G LDLR Ensembl:ENSG00000130164 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs925574630 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45258,RMVar_hsa_circ_51705,RMVar_hsa_circ_50951,RMVar_hsa_circ_347763,RMVar_hsa_circ_76246,RMVar_hsa_circ_192520,RMVar_hsa_circ_299753,RMVar_hsa_circ_336396,RMVar_hsa_circ_192524,RMVar_hsa_circ_286152,RMVar_hsa_circ_335001,RMVar_hsa_circ_192526 24441 RMVar_ID_24441 Human_SNP_ID_658403552 A-to-I Human chr19 + 11124333 11124333 11124333 ACCTCAAGTCATCTGCCTGCCTTGGCCCTGCCAAAGTGCTGGGATTATAGATGTGAGCCACCGCG ACCTCAAGTCATCTGCCTGCCTTGGCCCTGCCGAAGTGCTGGGATTATAGATGTGAGCCACCGCG A G LDLR Ensembl:ENSG00000130164 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs950322711 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13365033,Human_RBP_ID_17568441 RMVar_hsa_circ_45258,RMVar_hsa_circ_51705,RMVar_hsa_circ_50951,RMVar_hsa_circ_347763,RMVar_hsa_circ_76246,RMVar_hsa_circ_192520,RMVar_hsa_circ_299753,RMVar_hsa_circ_336396,RMVar_hsa_circ_192524,RMVar_hsa_circ_286152,RMVar_hsa_circ_335001,RMVar_hsa_circ_192526 24442 RMVar_ID_24442 Human_SNP_ID_658403937 A-to-I Human chr19 + 11125851 11125851 11125851 TTAGAATATTATTGGATTCCTGGGCAGGGCACAGTGGCTCACACCTGTAATCCCAGCACTTTGGG TTAGAATATTATTGGATTCCTGGGCAGGGCACTGTGGCTCACACCTGTAATCCCAGCACTTTGGG A T LDLR Ensembl:ENSG00000130164 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1416897719 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45258,RMVar_hsa_circ_51705,RMVar_hsa_circ_50951,RMVar_hsa_circ_347763,RMVar_hsa_circ_76246,RMVar_hsa_circ_192520,RMVar_hsa_circ_299753,RMVar_hsa_circ_336396,RMVar_hsa_circ_192524,RMVar_hsa_circ_286152,RMVar_hsa_circ_335001,RMVar_hsa_circ_192526 24443 RMVar_ID_24443 Human_SNP_ID_658403939 A-to-I Human chr19 + 11125861 11125861 11125861 ATTGGATTCCTGGGCAGGGCACAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGT ATTGGATTCCTGGGCAGGGCACAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGT A G LDLR Ensembl:ENSG00000130164 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1376768546 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45258,RMVar_hsa_circ_51705,RMVar_hsa_circ_50951,RMVar_hsa_circ_347763,RMVar_hsa_circ_76246,RMVar_hsa_circ_192520,RMVar_hsa_circ_299753,RMVar_hsa_circ_336396,RMVar_hsa_circ_192524,RMVar_hsa_circ_286152,RMVar_hsa_circ_335001,RMVar_hsa_circ_192526 24444 RMVar_ID_24444 Human_SNP_ID_658404317 A-to-I Human chr19 + 11127096 11127096 11127096 GAGTAGCTGGGATTACAGGTGCCCACCGCCACAGCTGGCTAATTTTTGTATTTTTAGTAGAGACA GAGTAGCTGGGATTACAGGTGCCCACCGCCACGGCTGGCTAATTTTTGTATTTTTAGTAGAGACA A G LDLR Ensembl:ENSG00000130164 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2569542 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45258,RMVar_hsa_circ_51705,RMVar_hsa_circ_50951,RMVar_hsa_circ_347763,RMVar_hsa_circ_76246,RMVar_hsa_circ_192520,RMVar_hsa_circ_299753,RMVar_hsa_circ_336396,RMVar_hsa_circ_192524,RMVar_hsa_circ_286152,RMVar_hsa_circ_335001,RMVar_hsa_circ_192526 24445 RMVar_ID_24445 Human_SNP_ID_658404409 A-to-I Human chr19 + 11127432 11127432 11127432 TAATTTTGTATTTTTAGTAGAGACAGGGTTTCACTATGTTGATCATGCTGGTCTCAAACTCCTGA TAATTTTGTATTTTTAGTAGAGACAGGGTTTCGCTATGTTGATCATGCTGGTCTCAAACTCCTGA A G LDLR Ensembl:ENSG00000130164 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1384650083 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45258,RMVar_hsa_circ_51705,RMVar_hsa_circ_50951,RMVar_hsa_circ_347763,RMVar_hsa_circ_76246,RMVar_hsa_circ_192520,RMVar_hsa_circ_299753,RMVar_hsa_circ_336396,RMVar_hsa_circ_192524,RMVar_hsa_circ_286152,RMVar_hsa_circ_335001,RMVar_hsa_circ_192526 24446 RMVar_ID_24446 Human_SNP_ID_658404478 A-to-I Human chr19 + 11127752 11127746 11127752 GAGGCAGGAGGATCTCTTGAGGCCAGGAGTTCAAGACAAGCCTGGGCAACATAGCCAGACCTCTG GAGGCAGGAGGATCTCTTGAGGCCAGG______AGACAAGCCTGGGCAACATAGCCAGACCTCTG GAGTTCA G LDLR Ensembl:ENSG00000130164 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1470365057 Functional Loss DEL dbSNP153 28..33 33 - - - RMVar_hsa_circ_45258,RMVar_hsa_circ_51705,RMVar_hsa_circ_50951,RMVar_hsa_circ_347763,RMVar_hsa_circ_76246,RMVar_hsa_circ_192520,RMVar_hsa_circ_299753,RMVar_hsa_circ_336396,RMVar_hsa_circ_192524,RMVar_hsa_circ_286152,RMVar_hsa_circ_335001,RMVar_hsa_circ_192526 24447 RMVar_ID_24447 Human_SNP_ID_658404516 A-to-I Human chr19 + 11127872 11127872 11127872 GATAACTCACAAATAAGCCCGTGTGGCCTCTCACAGACTTGGGAAGTTCTCCAAGTGTCCAGGGA GATAACTCACAAATAAGCCCGTGTGGCCTCTCGCAGACTTGGGAAGTTCTCCAAGTGTCCAGGGA A G LDLR Ensembl:ENSG00000130164 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2569538 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_93 GWAS_ID_2340,GWAS_ID_2341,GWAS_ID_2342,GWAS_ID_2343,GWAS_ID_2344 RMVar_hsa_circ_45258,RMVar_hsa_circ_51705,RMVar_hsa_circ_50951,RMVar_hsa_circ_347763,RMVar_hsa_circ_76246,RMVar_hsa_circ_192520,RMVar_hsa_circ_299753,RMVar_hsa_circ_336396,RMVar_hsa_circ_192524,RMVar_hsa_circ_286152,RMVar_hsa_circ_335001,RMVar_hsa_circ_192526 24448 RMVar_ID_24448 Human_SNP_ID_658404517 A-to-I Human chr19 + 11127872 11127872 11127872 GATAACTCACAAATAAGCCCGTGTGGCCTCTCACAGACTTGGGAAGTTCTCCAAGTGTCCAGGGA GATAACTCACAAATAAGCCCGTGTGGCCTCTCTCAGACTTGGGAAGTTCTCCAAGTGTCCAGGGA A T LDLR Ensembl:ENSG00000130164 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2569538 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_93 GWAS_ID_2340,GWAS_ID_2341,GWAS_ID_2342,GWAS_ID_2343,GWAS_ID_2344 RMVar_hsa_circ_45258,RMVar_hsa_circ_51705,RMVar_hsa_circ_50951,RMVar_hsa_circ_347763,RMVar_hsa_circ_76246,RMVar_hsa_circ_192520,RMVar_hsa_circ_299753,RMVar_hsa_circ_336396,RMVar_hsa_circ_192524,RMVar_hsa_circ_286152,RMVar_hsa_circ_335001,RMVar_hsa_circ_192526 24449 RMVar_ID_24449 Human_SNP_ID_658404832 A-to-I Human chr19 + 11128916 11128916 11128916 TGGGCAGGTGGCACGTGCCTGTGGTACCAGCTACTTGAGGGCCTGAGGCAGGAGGATCGCTTGAA TGGGCAGGTGGCACGTGCCTGTGGTACCAGCTGCTTGAGGGCCTGAGGCAGGAGGATCGCTTGAA A G LDLR Ensembl:ENSG00000130164 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1407886380 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45258,RMVar_hsa_circ_347763,RMVar_hsa_circ_336396,RMVar_hsa_circ_286152,RMVar_hsa_circ_192526,RMVar_hsa_circ_192527,RMVar_hsa_circ_283955 24450 RMVar_ID_24450 Human_SNP_ID_658405239 A-to-I Human chr19 + 11130083 11130083 11130083 AAAATTAGCCAGGCGTGGGAGTGGGCGCCTGTAATCCCAGCTACTCGGGAGGCCGAGGTAGAAAA AAAATTAGCCAGGCGTGGGAGTGGGCGCCTGTGATCCCAGCTACTCGGGAGGCCGAGGTAGAAAA A G LDLR Ensembl:ENSG00000130164 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1288649893 Functional Loss SNV dbSNP153 33..33 33 - - - 24451 RMVar_ID_24451 Human_SNP_ID_658405386 A-to-I Human chr19 + 11130667 11130667 11130667 CAGGTTGGAGTGCAGTGCTGTGATCTTGGCTCACTGCAACTTCTGCCTCCTGGGTTCAAGCAATT CAGGTTGGAGTGCAGTGCTGTGATCTTGGCTCCCTGCAACTTCTGCCTCCTGGGTTCAAGCAATT A C LDLR Ensembl:ENSG00000130164 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355423988 Functional Loss SNV dbSNP153 33..33 33 - - - 24452 RMVar_ID_24452 Human_SNP_ID_658405396 A-to-I Human chr19 + 11130716 11130716 11130716 CTGGGTTCAAGCAATTCTTATGCCTCAGCCTCAGCCTCCTGAGTAGCTGGGATTACAACACTATG CTGGGTTCAAGCAATTCTTATGCCTCAGCCTCTGCCTCCTGAGTAGCTGGGATTACAACACTATG A T LDLR Ensembl:ENSG00000130164 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1414011989 Functional Loss SNV dbSNP153 33..33 33 - - - 24453 RMVar_ID_24453 Human_SNP_ID_658409436 A-to-I Human chr19 - 11143934 11143934 11143934 GAGGCTGGAGTGCACTGGCATGATCTCGGCTCACTGCAGCCTCAACCTCCTGGGCTCAAGCAAAC GAGGCTGGAGTGCACTGGCATGATCTCGGCTCGCTGCAGCCTCAACCTCCTGGGCTCAAGCAAAC T C SPC24 Ensembl:ENSG00000161888 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1019318360 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23309216 24454 RMVar_ID_24454 Human_SNP_ID_658410057 A-to-I Human chr19 - 11146026 11146024 11146026 AAGGAGGCCAGGTGTGGTGGCTCATGCCTGCAATCCCAGCACTGTAGAAGGCAGAGGCCGGCAGA AAGGAGGCCAGGTGTGGTGGCTCATGCCTGCA__CCCAGCACTGTAGAAGGCAGAGGCCGGCAGA GAT G SPC24 Ensembl:ENSG00000161888 Protein coding intron GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs139936459 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_4500411,Human_RBP_ID_6718528,Human_RBP_ID_13365433,Human_RBP_ID_26472039,Human_RBP_ID_26982272,Human_RBP_ID_27267375,Human_RBP_ID_27463116 24455 RMVar_ID_24455 Human_SNP_ID_658410058 A-to-I Human chr19 - 11146026 11146026 11146026 AAGGAGGCCAGGTGTGGTGGCTCATGCCTGCAATCCCAGCACTGTAGAAGGCAGAGGCCGGCAGA AAGGAGGCCAGGTGTGGTGGCTCATGCCTGCAGTCCCAGCACTGTAGAAGGCAGAGGCCGGCAGA T C SPC24 Ensembl:ENSG00000161888 Protein coding intron GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs777684941 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4500411,Human_RBP_ID_6718528,Human_RBP_ID_13365433,Human_RBP_ID_26472039,Human_RBP_ID_26982272,Human_RBP_ID_27267375,Human_RBP_ID_27463116 24456 RMVar_ID_24456 Human_SNP_ID_658410244 A-to-I Human chr19 - 11146509 11146509 11146509 TGCCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGTCACCGCGCCTGGCCTTTTTTT TGCCCGCCTTGGCCTCCCAAAGTGCTGGGATTCCAGGTGTGAGTCACCGCGCCTGGCCTTTTTTT T G SPC24 Ensembl:ENSG00000161888 Protein coding intron GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831 HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line - 29129909,32596459 RNA-Seq:(High) rs1235638010 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1399500 24457 RMVar_ID_24457 Human_SNP_ID_658410255 A-to-I Human chr19 - 11146522 11146522 11146522 TGAGTTTGTGATCTGCCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGTCACCGCGC TGAGTTTGTGATCTGCCCGCCTTGGCCTCCCAGAGTGCTGGGATTACAGGTGTGAGTCACCGCGC T C SPC24 Ensembl:ENSG00000161888 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1200887615 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13365482 24458 RMVar_ID_24458 Human_SNP_ID_658410256 A-to-I Human chr19 - 11146523 11146523 11146523 CTGAGTTTGTGATCTGCCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGTCACCGCG CTGAGTTTGTGATCTGCCCGCCTTGGCCTCCCCAAGTGCTGGGATTACAGGTGTGAGTCACCGCG T G SPC24 Ensembl:ENSG00000161888 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1393741684 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13365482 24459 RMVar_ID_24459 Human_SNP_ID_658410302 A-to-I Human chr19 - 11146576 11146576 11146576 TATTTTTAGTAGAGACGGGGTTTCACCATGTTAGACAGGATGGTCTCCATCTCCTGAGTTTGTGA TATTTTTAGTAGAGACGGGGTTTCACCATGTTGGACAGGATGGTCTCCATCTCCTGAGTTTGTGA T C SPC24 Ensembl:ENSG00000161888 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs565003342 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26473529 24460 RMVar_ID_24460 Human_SNP_ID_658410309 A-to-I Human chr19 - 11146584 11146584 11146584 ATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTAGACAGGATGGTCTCCATCTCCTGA ATTTTTTGTATTTTTAGTAGAGACGGGGTTTCGCCATGTTAGACAGGATGGTCTCCATCTCCTGA T C SPC24 Ensembl:ENSG00000161888 Protein coding intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1187291995 Functional Loss SNV dbSNP153 33..33 33 - - - 24461 RMVar_ID_24461 Human_SNP_ID_658410341 A-to-I Human chr19 - 11146643 11146643 11146643 CTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCACCTGCCACCATGCGCAGCTAATTTTT CTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTGCAGGCACCTGCCACCATGCGCAGCTAATTTTT T C SPC24 Ensembl:ENSG00000161888 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1286021366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25382758 24462 RMVar_ID_24462 Human_SNP_ID_658410352 A-to-I Human chr19 - 11146678 11146678 11146678 CTGCAAGCTCCGCCTCCTCCCGGGTTCACGCCATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGA CTGCAAGCTCCGCCTCCTCCCGGGTTCACGCCGTTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGA T C SPC24 Ensembl:ENSG00000161888 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1190690925 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6718557,Human_RBP_ID_13365483,Human_RBP_ID_23173788,Human_RBP_ID_26464283,Human_RBP_ID_27463123 24463 RMVar_ID_24463 Human_SNP_ID_658410371 A-to-I Human chr19 - 11146716 11146716 11146716 TCGCCCAGGCTGGAGTGCAGTGGTGCGATCTCAGCTCACTGCAAGCTCCGCCTCCTCCCGGGTTC TCGCCCAGGCTGGAGTGCAGTGGTGCGATCTCTGCTCACTGCAAGCTCCGCCTCCTCCCGGGTTC T A SPC24 Ensembl:ENSG00000161888 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229,31158229 RNA-Seq:(High) rs545951983 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4500438,Human_RBP_ID_6718558,Human_RBP_ID_13365483,Human_RBP_ID_26464284 Clinvar_Rec_94 24464 RMVar_ID_24464 Human_SNP_ID_658410372 A-to-I Human chr19 - 11146716 11146716 11146716 TCGCCCAGGCTGGAGTGCAGTGGTGCGATCTCAGCTCACTGCAAGCTCCGCCTCCTCCCGGGTTC TCGCCCAGGCTGGAGTGCAGTGGTGCGATCTCGGCTCACTGCAAGCTCCGCCTCCTCCCGGGTTC T C SPC24 Ensembl:ENSG00000161888 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229,31158229 RNA-Seq:(High) rs545951983 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4500438,Human_RBP_ID_6718558,Human_RBP_ID_13365483,Human_RBP_ID_26464284 Clinvar_Rec_94 24465 RMVar_ID_24465 Human_SNP_ID_658410373 A-to-I Human chr19 - 11146716 11146716 11146716 TCGCCCAGGCTGGAGTGCAGTGGTGCGATCTCAGCTCACTGCAAGCTCCGCCTCCTCCCGGGTTC TCGCCCAGGCTGGAGTGCAGTGGTGCGATCTCCGCTCACTGCAAGCTCCGCCTCCTCCCGGGTTC T G SPC24 Ensembl:ENSG00000161888 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229,31158229 RNA-Seq:(High) rs545951983 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4500438,Human_RBP_ID_6718558,Human_RBP_ID_13365483,Human_RBP_ID_26464284 Clinvar_Rec_94 24466 RMVar_ID_24466 Human_SNP_ID_658410446 A-to-I Human chr19 - 11146826 11146826 11146826 TCCACCCGCCCGCCTTGGCCTCCCAAAGTGCTAGGATTCCAGGCGTGAGCCATCGTGCCCAGCTA TCCACCCGCCCGCCTTGGCCTCCCAAAGTGCTGGGATTCCAGGCGTGAGCCATCGTGCCCAGCTA T C SPC24 Ensembl:ENSG00000161888 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs150519327 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13365487,Human_RBP_ID_23173790 24467 RMVar_ID_24467 Human_SNP_ID_658410464 A-to-I Human chr19 - 11146901 11146901 11146901 TAATTTTTTGTATTTGGTAGAGATGGAGTTTCACCATGGTGGTCAGGCTGGTCTTGAACTCCTGA TAATTTTTTGTATTTGGTAGAGATGGAGTTTCGCCATGGTGGTCAGGCTGGTCTTGAACTCCTGA T C SPC24 Ensembl:ENSG00000161888 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs537388811 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_512755,Human_RBP_ID_1291989,Human_RBP_ID_6718564,Human_RBP_ID_9084353,Human_RBP_ID_9329779,Human_RBP_ID_13365491,Human_RBP_ID_23173792,Human_RBP_ID_26472042 24468 RMVar_ID_24468 Human_SNP_ID_658410490 A-to-I Human chr19 - 11146958 11146958 11146958 CTCCTGCCTCAGCCTCCAAAGTAGCTGGGATTACAGGCATGCGCCACCACACCCAGCTAATTTTT CTCCTGCCTCAGCCTCCAAAGTAGCTGGGATTCCAGGCATGCGCCACCACACCCAGCTAATTTTT T G SPC24 Ensembl:ENSG00000161888 Protein coding intron GSE38233;GSE99789;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29796672,32596459 RNA-Seq:(High) rs1172158820 Functional Loss SNV dbSNP153 33..33 33 - - - 24469 RMVar_ID_24469 Human_SNP_ID_658410503 A-to-I Human chr19 - 11147041 11147041 11147041 AGTTTCACTCTTGTTGTCCAGTCTGGAGTGCAATGGCACAATCTCAGCTCACAGCAACCTCTGCC AGTTTCACTCTTGTTGTCCAGTCTGGAGTGCAGTGGCACAATCTCAGCTCACAGCAACCTCTGCC T C SPC24 Ensembl:ENSG00000161888 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1443128487 Functional Loss SNV dbSNP153 33..33 33 - - - 24470 RMVar_ID_24470 Human_SNP_ID_658410657 A-to-I Human chr19 - 11147428 11147428 11147428 TAACCACTGGAGGTGGAGGTTGCAATGAGCCGAGATCGCACCACTGTACTCCAGCCTGGCCTACA TAACCACTGGAGGTGGAGGTTGCAATGAGCCGCGATCGCACCACTGTACTCCAGCCTGGCCTACA T G SPC24 Ensembl:ENSG00000161888 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1022755985 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13365524 RMVar_hsa_circ_79112,RMVar_hsa_circ_123153,RMVar_hsa_circ_86595,RMVar_hsa_circ_192529,RMVar_hsa_circ_192531,RMVar_hsa_circ_76473,RMVar_hsa_circ_192530,RMVar_hsa_circ_192528 24471 RMVar_ID_24471 Human_SNP_ID_658411595 A-to-I Human chr19 - 11150485 11150485 11150485 GCCACCAGTAGCCTTTTTTCTTTTTTTTTTTTAAGATGGAGTCTTGCTCTATCGCCCAGACTGGA GCCACCAGTAGCCTTTTTTCTTTTTTTTTTTTTAGATGGAGTCTTGCTCTATCGCCCAGACTGGA T A SPC24 Ensembl:ENSG00000161888 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1459555389 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13365596 RMVar_hsa_circ_86595,RMVar_hsa_circ_192528 24472 RMVar_ID_24472 Human_SNP_ID_658412770 A-to-I Human chr19 - 11154356 11154356 11154356 GTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCTAGGCTGGTCTTAAACTCCCAGCCT GTTTGTATTTTTAGTAGAGATGGGGTTTCACCGTGTTGGCTAGGCTGGTCTTAAACTCCCAGCCT T C SPC24 Ensembl:ENSG00000161888 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs143062905 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86595,RMVar_hsa_circ_192528 24473 RMVar_ID_24473 Human_SNP_ID_658412808 A-to-I Human chr19 - 11154572 11154570 11154572 TGTCCTCCAGGTTCATCCATGTCATAGCCTGTATCAGAATTTCCTTTCATTTTGTGTACTTACTG TGTCCTCCAGGTTCATCCATGTCATAGCCTGT__CAGAATTTCCTTTCATTTTGTGTACTTACTG GAT G SPC24 Ensembl:ENSG00000161888 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs981873965 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_86595,RMVar_hsa_circ_192528 24474 RMVar_ID_24474 Human_SNP_ID_658412809 A-to-I Human chr19 - 11154572 11154572 11154572 TGTCCTCCAGGTTCATCCATGTCATAGCCTGTATCAGAATTTCCTTTCATTTTGTGTACTTACTG TGTCCTCCAGGTTCATCCATGTCATAGCCTGTGTCAGAATTTCCTTTCATTTTGTGTACTTACTG T C SPC24 Ensembl:ENSG00000161888 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10402457 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2345,GWAS_ID_2346,GWAS_ID_2347,GWAS_ID_2348,GWAS_ID_2349,GWAS_ID_2350,GWAS_ID_2351,GWAS_ID_2352 RMVar_hsa_circ_86595,RMVar_hsa_circ_192528 24475 RMVar_ID_24475 Human_SNP_ID_658416658 A-to-I Human chr19 - 11168095 11168095 11168095 TGGAGGCTTAGGCGGGAGAATCACTTGAACCCAGGAGGTGGAGGTTGCAGTGAGCCAGAGATCAT TGGAGGCTTAGGCGGGAGAATCACTTGAACCCGGGAGGTGGAGGTTGCAGTGAGCCAGAGATCAT T C KANK2 Ensembl:ENSG00000197256 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs534587065 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77650,RMVar_hsa_circ_192534 24476 RMVar_ID_24476 Human_SNP_ID_658416914 A-to-I Human chr19 - 11169146 11169146 11169146 TTTAGTAGAGATGGGATTTCACTGTGTTGGCCAGGCTGGTCTTGAACTCCTGAGCTCAAGTGATC TTTAGTAGAGATGGGATTTCACTGTGTTGGCCGGGCTGGTCTTGAACTCCTGAGCTCAAGTGATC T C KANK2 Ensembl:ENSG00000197256 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs918401267 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77650,RMVar_hsa_circ_192534 24477 RMVar_ID_24477 Human_SNP_ID_658420330 A-to-I Human chr19 - 11180044 11180044 11180044 CAGCCTGGGCAATATAGTGAAACCCCATCTCTACAAACATTACAGAAAATTAGCTGGGCACAGTG CAGCCTGGGCAATATAGTGAAACCCCATCTCTGCAAACATTACAGAAAATTAGCTGGGCACAGTG T C KANK2 Ensembl:ENSG00000197256 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1230308462 Functional Loss SNV dbSNP153 33..33 33 - - - 24478 RMVar_ID_24478 Human_SNP_ID_658461290 A-to-I Human chr19 - 11320548 11320548 11320548 CCACTTCAGCCTCCTGAGTTTCTGGAACTACAAGCAAGCACCACCACATCCAGCTGATTGAGTGA CCACTTCAGCCTCCTGAGTTTCTGGAACTACAGGCAAGCACCACCACATCCAGCTGATTGAGTGA T C AC011472.2 Ensembl:ENSG00000267174 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1568297083 Functional Loss SNV dbSNP153 33..33 33 - - - 24479 RMVar_ID_24479 Human_SNP_ID_658477770 A-to-I Human chr19 - 11379568 11379567 11379569 GAGGAGTTTGGAATTTTTTTTTTTTTTGAGACAGAGTCACTCTTGTCGCCCAAGCTGTAGTGCAG GAGGAGTTTGGAATTTTTTTTTTTTTTGAGA__GAGTCACTCTTGTCGCCCAAGCTGTAGTGCAG CTG C EPOR Ensembl:ENSG00000187266 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928009344 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_17568448 24480 RMVar_ID_24480 Human_SNP_ID_658481244 A-to-I Human chr19 - 11390211 11390201 11390211 AACATGCTTTTTTTTTTTTTTTTTTTTGAGACAGAGTCTTGCTTTGTCGCCCAGGCTGGAGTGCA AACATGCTTTTTTTTTTTTTTTTTTTTGAGAC__________TTTGTCGCCCAGGCTGGAGTGCA AGCAAGACTCT A RGL3 Ensembl:ENSG00000205517 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1439065211 Functional Loss DEL dbSNP153 33..42 33 - - - 24481 RMVar_ID_24481 Human_SNP_ID_658482494 A-to-I Human chr19 - 11394933 11394933 11394933 ATGTGCCACCATGCCTAGCTCATTTTTTTGGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGG ATGTGCCACCATGCCTAGCTCATTTTTTTGGTGTTTTTAGTAGAGACGGGGTTTCACCATGTTGG T C RGL3 Ensembl:ENSG00000205517 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1401920250 Functional Loss SNV dbSNP153 33..33 33 - - - 24482 RMVar_ID_24482 Human_SNP_ID_658483172 A-to-I Human chr19 - 11396806 11396806 11396806 AAAATTAGTCGGGTGTGGTGGCACACTCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGA AAAATTAGTCGGGTGTGGTGGCACACTCCTGTGGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGA T C RGL3 Ensembl:ENSG00000205517 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1138134 Functional Loss SNV dbSNP153 33..33 33 - - - 24483 RMVar_ID_24483 Human_SNP_ID_658489475 A-to-I Human chr19 - 11416325 11416325 11416325 AAAGGTAGCTGGGTGTGGTGGCGCATGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGTTGCAGT AAAGGTAGCTGGGTGTGGTGGCGCATGCCTGTTGTCCCAGCTACTCGGGAGGCTGAGGTTGCAGT T A RGL3 Ensembl:ENSG00000205517 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1486187631 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_46114,RMVar_hsa_circ_313692,RMVar_hsa_circ_325593,RMVar_hsa_circ_274391 24484 RMVar_ID_24484 Human_SNP_ID_658497418 A-to-I Human chr19 - 11435634 11435634 11435634 TGTCCAGCAGCCGCGGTTCCTGCTGCAGAAAGAAAGCGGAAATTTCTGGACCCCGTCACTTCCGG TGTCCAGCAGCCGCGGTTCCTGCTGCAGAAAGCAAGCGGAAATTTCTGGACCCCGTCACTTCCGG T G CCDC151 Ensembl:ENSG00000198003 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs150481283 Functional Loss SNV dbSNP153 33..33 33 - - - 24485 RMVar_ID_24485 Human_SNP_ID_658498675 A-to-I Human chr19 + 11438939 11438939 11438939 TTATTTATTTATATTTTTTGAGACAGGGTCTCACTCTGTCGCCCAGGCTGGAGTGCAGTGGCGTG TTATTTATTTATATTTTTTGAGACAGGGTCTCGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCGTG A G PRKCSH Ensembl:ENSG00000130175 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1382634504 Functional Loss SNV dbSNP153 33..33 33 - - - 24486 RMVar_ID_24486 Human_SNP_ID_658498790 A-to-I Human chr19 + 11439315 11439315 11439315 ATAAGACCCGGCTCATGGTGGCTCCTGCCTGTAATCCCAGCATTTTGGGAGGCTGAGGCAGGAAG ATAAGACCCGGCTCATGGTGGCTCCTGCCTGTGATCCCAGCATTTTGGGAGGCTGAGGCAGGAAG A G PRKCSH Ensembl:ENSG00000130175 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs551635444 Functional Loss SNV dbSNP153 33..33 33 - - - 24487 RMVar_ID_24487 Human_SNP_ID_658498966 A-to-I Human chr19 + 11439720 11439720 11439720 TCGGCTCACTCTAACCTCTGCCTCCCGGGTTCAAGCGATTCTTCTGCCTTAGCCTCCTGAGTAGC TCGGCTCACTCTAACCTCTGCCTCCCGGGTTCGAGCGATTCTTCTGCCTTAGCCTCCTGAGTAGC A G PRKCSH Ensembl:ENSG00000130175 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1323760363 Functional Loss SNV dbSNP153 33..33 33 - - - 24488 RMVar_ID_24488 Human_SNP_ID_658498972 A-to-I Human chr19 + 11439738 11439738 11439738 TGCCTCCCGGGTTCAAGCGATTCTTCTGCCTTAGCCTCCTGAGTAGCTGGGACTACAGGCATCCA TGCCTCCCGGGTTCAAGCGATTCTTCTGCCTTTGCCTCCTGAGTAGCTGGGACTACAGGCATCCA A T PRKCSH Ensembl:ENSG00000130175 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1280414417 Functional Loss SNV dbSNP153 33..33 33 - - - 24489 RMVar_ID_24489 Human_SNP_ID_658498997 A-to-I Human chr19 + 11439823 11439823 11439823 TTGTATTTTTAGTAGAGACGGTGTTTCACAATATTGGCCAGGCTGGTCTCGAACTCCTGACCTCA TTGTATTTTTAGTAGAGACGGTGTTTCACAATCTTGGCCAGGCTGGTCTCGAACTCCTGACCTCA A C PRKCSH Ensembl:ENSG00000130175 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs762002499 Functional Loss SNV dbSNP153 33..33 33 - - - 24490 RMVar_ID_24490 Human_SNP_ID_658499047 A-to-I Human chr19 + 11440013 11440013 11440013 AGGCTGAGGCAGGAAGATTGCTTGGGCCTGGGAAGCAGAGGTTGCAGTGAGCTAAAAAGTAAAAA AGGCTGAGGCAGGAAGATTGCTTGGGCCTGGGGAGCAGAGGTTGCAGTGAGCTAAAAAGTAAAAA A G PRKCSH Ensembl:ENSG00000130175 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1449750234 Functional Loss SNV dbSNP153 33..33 33 - - - 24491 RMVar_ID_24491 Human_SNP_ID_658499049 A-to-I Human chr19 + 11440017 11440017 11440017 TGAGGCAGGAAGATTGCTTGGGCCTGGGAAGCAGAGGTTGCAGTGAGCTAAAAAGTAAAAAAAAA TGAGGCAGGAAGATTGCTTGGGCCTGGGAAGCGGAGGTTGCAGTGAGCTAAAAAGTAAAAAAAAA A G PRKCSH Ensembl:ENSG00000130175 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1210140481 Functional Loss SNV dbSNP153 33..33 33 - - - 24492 RMVar_ID_24492 Human_SNP_ID_658499418 A-to-I Human chr19 + 11441257 11441255 11441257 GTCTCCGCACCGCAGAGAGAAGGGCCGTAAGGAGAGAGAGTCCCTGCAGCAGATGGCCGAGGTCA GTCTCCGCACCGCAGAGAGAAGGGCCGTAAG__GAGAGAGTCCCTGCAGCAGATGGCCGAGGTCA GGA G PRKCSH Ensembl:ENSG00000130175 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs779685748 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_771505,Human_RBP_ID_825089,Human_RBP_ID_912374,Human_RBP_ID_3954512,Human_RBP_ID_18470507,Human_RBP_ID_18722085,Human_RBP_ID_22447415,Human_RBP_ID_22533115,Human_RBP_ID_22762757,Human_RBP_ID_26334858,Human_RBP_ID_27463201 Human_Splice_Rec_1960668,Human_Splice_Rec_1960706,Human_Splice_Rec_1960722,Human_Splice_Rec_1960742,Human_Splice_Rec_1960752,Human_Splice_Rec_1960786,Human_Splice_Rec_1960794,Human_Splice_Rec_1960826 RMVar_hsa_circ_192595,RMVar_hsa_circ_346963 24493 RMVar_ID_24493 Human_SNP_ID_658500046 A-to-I Human chr19 + 11443355 11443355 11443355 AGATCACGAGGTCAGGAGATTGAGACCATCTTAGCCAACATGGTGAAACCCATCTCTACTAAAAA AGATCACGAGGTCAGGAGATTGAGACCATCTTGGCCAACATGGTGAAACCCATCTCTACTAAAAA A G PRKCSH Ensembl:ENSG00000130175 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1198957573 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88582,RMVar_hsa_circ_192596 24494 RMVar_ID_24494 Human_SNP_ID_658500050 A-to-I Human chr19 + 11443362 11443362 11443362 GAGGTCAGGAGATTGAGACCATCTTAGCCAACATGGTGAAACCCATCTCTACTAAAAATACAAAA GAGGTCAGGAGATTGAGACCATCTTAGCCAACGTGGTGAAACCCATCTCTACTAAAAATACAAAA A G PRKCSH Ensembl:ENSG00000130175 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1048420360 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88582,RMVar_hsa_circ_192596 24495 RMVar_ID_24495 Human_SNP_ID_658502290 A-to-I Human chr19 + 11449612 11449612 11449612 TGGCCCAGGCTGGAGTGCAGTGATGCGACCTCAGCTGACTGCAACCTCTACCTCCCGGGTTCAAA TGGCCCAGGCTGGAGTGCAGTGATGCGACCTCGGCTGACTGCAACCTCTACCTCCCGGGTTCAAA A G PRKCSH Ensembl:ENSG00000130175 Protein coding intron GSE38233;GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;ASD brains,temporal_cortex;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,30559470,31158229,31158229 RNA-Seq:(High) rs1325861026 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1554168,Human_RBP_ID_1879879,Human_RBP_ID_8476850,Human_RBP_ID_13365995,Human_RBP_ID_23173856,Human_RBP_ID_23309229,Human_RBP_ID_26464339,Human_RBP_ID_27463206 RMVar_hsa_circ_112721,RMVar_hsa_circ_192600 24496 RMVar_ID_24496 Human_SNP_ID_658502363 A-to-I Human chr19 + 11449862 11449862 11449862 CGGCCATCTCCTGCCTTTTTTTTTTTGGATGGAGTTTCACTCTTGTTGCCGAGGCTGGAATGTGG CGGCCATCTCCTGCCTTTTTTTTTTTGGATGGGGTTTCACTCTTGTTGCCGAGGCTGGAATGTGG A G PRKCSH Ensembl:ENSG00000130175 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1162460600 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13366005,Human_RBP_ID_17568939,Human_RBP_ID_22966659,Human_RBP_ID_23173860,Human_RBP_ID_23309230,Human_RBP_ID_23781764,Human_RBP_ID_26464344 RMVar_hsa_circ_112721,RMVar_hsa_circ_192600 24497 RMVar_ID_24497 Human_SNP_ID_658502372 A-to-I Human chr19 + 11449900 11449899 11449900 ACTCTTGTTGCCGAGGCTGGAATGTGGAATGCAATGGCGCGATCTCGGCTCACTGCAACCTCCAC ACTCTTGTTGCCGAGGCTGGAATGTGGAATGC_ATGGCGCGATCTCGGCTCACTGCAACCTCCAC CA C PRKCSH Ensembl:ENSG00000130175 Protein coding intron GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,29796672,31158229,31158229,31158229 RNA-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 24498 RMVar_ID_24498 Human_SNP_ID_658502374 A-to-I Human chr19 + 11449900 11449900 11449900 ACTCTTGTTGCCGAGGCTGGAATGTGGAATGCAATGGCGCGATCTCGGCTCACTGCAACCTCCAC ACTCTTGTTGCCGAGGCTGGAATGTGGAATGCGATGGCGCGATCTCGGCTCACTGCAACCTCCAC A G PRKCSH Ensembl:ENSG00000130175 Protein coding intron GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,29796672,31158229,31158229,31158229 RNA-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 24499 RMVar_ID_24499 Human_SNP_ID_658502403 A-to-I Human chr19 + 11449984 11449984 11449984 CTCCTGCCTCAGCCTCCTGAGTAATTGGGACTACAGGCGCCGCCACCACGCCTGGCTAATTTTTT CTCCTGCCTCAGCCTCCTGAGTAATTGGGACTGCAGGCGCCGCCACCACGCCTGGCTAATTTTTT A G PRKCSH Ensembl:ENSG00000130175 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1200537589 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13366011,Human_RBP_ID_26464347 RMVar_hsa_circ_112721,RMVar_hsa_circ_192600 24500 RMVar_ID_24500 Human_SNP_ID_658502414 A-to-I Human chr19 + 11450020 11450020 11450020 GCGCCGCCACCACGCCTGGCTAATTTTTTTGTATTTTTAGTAGAGATGGGGTTTCCCTGTGTTAA GCGCCGCCACCACGCCTGGCTAATTTTTTTGTGTTTTTAGTAGAGATGGGGTTTCCCTGTGTTAA A G PRKCSH Ensembl:ENSG00000130175 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1440049301 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112721,RMVar_hsa_circ_192600 24501 RMVar_ID_24501 Human_SNP_ID_658502422 A-to-I Human chr19 + 11450055 11450055 11450055 TTTAGTAGAGATGGGGTTTCCCTGTGTTAACCAGGTTGGTCTCGATCTCCTGACCTCGTGATCCG TTTAGTAGAGATGGGGTTTCCCTGTGTTAACCCGGTTGGTCTCGATCTCCTGACCTCGTGATCCG A C PRKCSH Ensembl:ENSG00000130175 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1279620461 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112721,RMVar_hsa_circ_192600 24502 RMVar_ID_24502 Human_SNP_ID_658502501 A-to-I Human chr19 + 11450356 11450356 11450356 AAAATTAGCTGGGTGTGGTGGTAGGTGCCTGTAGTTCCAGCTGCTCAAGAGGCTGAAGCACAAGA AAAATTAGCTGGGTGTGGTGGTAGGTGCCTGTGGTTCCAGCTGCTCAAGAGGCTGAAGCACAAGA A G PRKCSH Ensembl:ENSG00000130175 Protein coding intron GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,29796672,31158229,31158229,31158229 RNA-Seq:(High) rs1361666865 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17567949,Human_RBP_ID_23173867,Human_RBP_ID_26464348 RMVar_hsa_circ_112721,RMVar_hsa_circ_192600 24503 RMVar_ID_24503 Human_SNP_ID_658502511 A-to-I Human chr19 + 11450402 11450402 11450402 AAGAGGCTGAAGCACAAGAATCACTTGAACCCAGGAGGTAGAGGTTGGAGTGAGCCAAGATCATG AAGAGGCTGAAGCACAAGAATCACTTGAACCCGGGAGGTAGAGGTTGGAGTGAGCCAAGATCATG A G PRKCSH Ensembl:ENSG00000130175 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1321591536 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17567949 RMVar_hsa_circ_112721,RMVar_hsa_circ_192600 24504 RMVar_ID_24504 Human_SNP_ID_658502517 A-to-I Human chr19 + 11450426 11450426 11450426 TTGAACCCAGGAGGTAGAGGTTGGAGTGAGCCAAGATCATGCTACTGCACTCTCCAGCCTGGGCT TTGAACCCAGGAGGTAGAGGTTGGAGTGAGCCGAGATCATGCTACTGCACTCTCCAGCCTGGGCT A G PRKCSH Ensembl:ENSG00000130175 Protein coding intron GSE47997;GSE38233;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;cultured B-cells;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 23474544,24183664,29796672,31158229,31158229 RNA-Seq:(High) rs1014752036 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9908650,Human_RBP_ID_17567950,Human_RBP_ID_22978357,Human_RBP_ID_23173868,Human_RBP_ID_23309231,Human_RBP_ID_25441981,Human_RBP_ID_26464349 RMVar_hsa_circ_112721,RMVar_hsa_circ_192600 24505 RMVar_ID_24505 Human_SNP_ID_658502526 A-to-I Human chr19 + 11450459 11450459 11450459 AGATCATGCTACTGCACTCTCCAGCCTGGGCTACAGAGTGAGACTCTCAAAAAAAAAAAATAATA AGATCATGCTACTGCACTCTCCAGCCTGGGCTCCAGAGTGAGACTCTCAAAAAAAAAAAATAATA A C PRKCSH Ensembl:ENSG00000130175 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs776848744 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_138023,Human_RBP_ID_13366016,Human_RBP_ID_17567950,Human_RBP_ID_26472055 RMVar_hsa_circ_112721,RMVar_hsa_circ_192600 24506 RMVar_ID_24506 Human_SNP_ID_658502527 A-to-I Human chr19 + 11450459 11450459 11450459 AGATCATGCTACTGCACTCTCCAGCCTGGGCTACAGAGTGAGACTCTCAAAAAAAAAAAATAATA AGATCATGCTACTGCACTCTCCAGCCTGGGCTGCAGAGTGAGACTCTCAAAAAAAAAAAATAATA A G PRKCSH Ensembl:ENSG00000130175 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs776848744 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_138023,Human_RBP_ID_13366016,Human_RBP_ID_17567950,Human_RBP_ID_26472055 RMVar_hsa_circ_112721,RMVar_hsa_circ_192600 24507 RMVar_ID_24507 Human_SNP_ID_658502569 A-to-I Human chr19 + 11450543 11450543 11450543 AAGGTCTCCAGGCTGGTCAACTCCTGGCCTCAAATGATCCTCCCACCTCAGCCTCCCAAGCAGCC AAGGTCTCCAGGCTGGTCAACTCCTGGCCTCAGATGATCCTCCCACCTCAGCCTCCCAAGCAGCC A G PRKCSH Ensembl:ENSG00000130175 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1287804513 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_138023,Human_RBP_ID_17568450,Human_RBP_ID_23173870,Human_RBP_ID_26464353,Human_RBP_ID_27463208 RMVar_hsa_circ_112721,RMVar_hsa_circ_192600 24508 RMVar_ID_24508 Human_SNP_ID_658502576 A-to-I Human chr19 + 11450568 11450568 11450568 GGCCTCAAATGATCCTCCCACCTCAGCCTCCCAAGCAGCCGGGACTACAGGCAAACATCACCATG GGCCTCAAATGATCCTCCCACCTCAGCCTCCCGAGCAGCCGGGACTACAGGCAAACATCACCATG A G PRKCSH Ensembl:ENSG00000130175 Protein coding intron GSE47997;GSE38233;GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,29129909,32596459 RNA-Seq:(High) rs1165166530 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_138023,Human_RBP_ID_17568450,Human_RBP_ID_27463208 RMVar_hsa_circ_112721,RMVar_hsa_circ_192600 24509 RMVar_ID_24509 Human_SNP_ID_658502579 A-to-I Human chr19 + 11450582 11450582 11450582 CTCCCACCTCAGCCTCCCAAGCAGCCGGGACTACAGGCAAACATCACCATGTCCAGCTGTCCCCA CTCCCACCTCAGCCTCCCAAGCAGCCGGGACTGCAGGCAAACATCACCATGTCCAGCTGTCCCCA A G PRKCSH Ensembl:ENSG00000130175 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs995176160 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_138023,Human_RBP_ID_17568450,Human_RBP_ID_26464354 RMVar_hsa_circ_112721,RMVar_hsa_circ_192600 24510 RMVar_ID_24510 Human_SNP_ID_658508411 A-to-I Human chr19 - 11467930 11467930 11467930 TTAAAATTAACCAGACATGGTGGCATGCGCCTATTGTTCCAGCTACTTGGGAGGCTGAGGTGGGA TTAAAATTAACCAGACATGGTGGCATGCGCCTGTTGTTCCAGCTACTTGGGAGGCTGAGGTGGGA T C ELAVL3,AC008481.3 Ensembl:ENSG00000196361,Ensembl:ENSG00000267477 Protein coding,Protein coding intron,intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs915941944 Functional Loss SNV dbSNP153 33..33 33 - - - 24511 RMVar_ID_24511 Human_SNP_ID_658508694 A-to-I Human chr19 - 11469058 11469058 11469058 AAAAGTAGCCAGGCTTGGAGGCGCATACCTGTAGCCCCAAGTACTGGGGAGGCTGACGTGGGAGG AAAAGTAGCCAGGCTTGGAGGCGCATACCTGTCGCCCCAAGTACTGGGGAGGCTGACGTGGGAGG T G ELAVL3,AC008481.3 Ensembl:ENSG00000196361,Ensembl:ENSG00000267477 Protein coding,Protein coding intron,intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs953866518 Functional Loss SNV dbSNP153 33..33 33 - - - 24512 RMVar_ID_24512 Human_SNP_ID_658508700 A-to-I Human chr19 - 11469080 11469080 11469080 CTACTAAAAATACAAAGAAAAAAAAAGTAGCCAGGCTTGGAGGCGCATACCTGTAGCCCCAAGTA CTACTAAAAATACAAAGAAAAAAAAAGTAGCCGGGCTTGGAGGCGCATACCTGTAGCCCCAAGTA T C ELAVL3,AC008481.3 Ensembl:ENSG00000196361,Ensembl:ENSG00000267477 Protein coding,Protein coding intron,intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1015882834 Functional Loss SNV dbSNP153 33..33 33 - - - 24513 RMVar_ID_24513 Human_SNP_ID_658508922 A-to-I Human chr19 - 11469828 11469828 11469828 GTCTCGAGCTCTTGAGCTCAAGCAATCCGTCCACCTTGGCCTCCCAAAGTGCTGGAATTACAGGC GTCTCGAGCTCTTGAGCTCAAGCAATCCGTCCGCCTTGGCCTCCCAAAGTGCTGGAATTACAGGC T C ELAVL3,AC008481.3 Ensembl:ENSG00000196361,Ensembl:ENSG00000267477 Protein coding,Protein coding intron,intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs577064482 Functional Loss SNV dbSNP153 33..33 33 - - - 24514 RMVar_ID_24514 Human_SNP_ID_658508923 A-to-I Human chr19 - 11469828 11469828 11469828 GTCTCGAGCTCTTGAGCTCAAGCAATCCGTCCACCTTGGCCTCCCAAAGTGCTGGAATTACAGGC GTCTCGAGCTCTTGAGCTCAAGCAATCCGTCCCCCTTGGCCTCCCAAAGTGCTGGAATTACAGGC T G ELAVL3,AC008481.3 Ensembl:ENSG00000196361,Ensembl:ENSG00000267477 Protein coding,Protein coding intron,intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs577064482 Functional Loss SNV dbSNP153 33..33 33 - - - 24515 RMVar_ID_24515 Human_SNP_ID_658516252 A-to-I Human chr19 - 11494507 11494507 11494507 TTTTGTATTTTTAGTAGACACTGGGTTTCACCATGTTGGCCGGCTGGTCTTGAACTCCTGACCTC TTTTGTATTTTTAGTAGACACTGGGTTTCACCGTGTTGGCCGGCTGGTCTTGAACTCCTGACCTC T C ZNF653,AC008481.3 Ensembl:ENSG00000161914,Ensembl:ENSG00000267477 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs371608482 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128196,RMVar_hsa_circ_192610,RMVar_hsa_circ_23942 24516 RMVar_ID_24516 Human_SNP_ID_658519588 A-to-I Human chr19 - 11506061 11506061 11506061 TTTCCTGCTTGGGGCTCTCTTCCCTCATCTCTAGCAGTATGGCATCCCCTCCCCAGGATCTCGGG TTTCCTGCTTGGGGCTCTCTTCCCTCATCTCTGGCAGTATGGCATCCCCTCCCCAGGATCTCGGG T C ECSIT Ensembl:ENSG00000130159 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs929008981 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_140049,Human_RBP_ID_512926,Human_RBP_ID_9329782,Human_RBP_ID_17656769,Human_RBP_ID_21892144,Human_RBP_ID_22064949,Human_RBP_ID_27267502,Human_RBP_ID_27463219 24517 RMVar_ID_24517 Human_SNP_ID_658520200 A-to-I Human chr19 - 11507757 11507757 11507757 TGTTGAGGGCCCCTTCTCCCTGTGGCTCCGCAACAAGTGTGTGTATTACCACATCCTCAGAGCTG TGTTGAGGGCCCCTTCTCCCTGTGGCTCCGCAGCAAGTGTGTGTATTACCACATCCTCAGAGCTG T C ECSIT Ensembl:ENSG00000130159 Protein coding intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1211497782 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_512935 Human_Splice_Rec_1961008,Human_Splice_Rec_1961009,Human_Splice_Rec_1961030,Human_Splice_Rec_1961031,Human_Splice_Rec_1961040,Human_Splice_Rec_1961041,Human_Splice_Rec_1961057,Human_Splice_Rec_1961067,Human_Splice_Rec_1961078,Human_Splice_Rec_1961079,Human_Splice_Rec_1961088 RMVar_hsa_circ_272282,RMVar_hsa_circ_343331,RMVar_hsa_circ_324078,RMVar_hsa_circ_192613 24518 RMVar_ID_24518 Human_SNP_ID_658520831 A-to-I Human chr19 - 11509972 11509972 11509972 CTAGCTACTTGCGAGGGTGAGGCAGGAGAATCACTTGAACCCAGGAGGTGGAGGTTGCAGTGAGC CTAGCTACTTGCGAGGGTGAGGCAGGAGAATCTCTTGAACCCAGGAGGTGGAGGTTGCAGTGAGC T A ECSIT Ensembl:ENSG00000130159 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1163550655 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_343331,RMVar_hsa_circ_324078,RMVar_hsa_circ_192614,RMVar_hsa_circ_113884 24519 RMVar_ID_24519 Human_SNP_ID_658523398 A-to-I Human chr19 - 11519478 11519478 11519478 AAACTATTTTCAAATTAGCTGGGCATGGTGGCACGCGTCTGTAGTCCCAGCTTCTCGACGCTCTG AAACTATTTTCAAATTAGCTGGGCATGGTGGCGCGCGTCTGTAGTCCCAGCTTCTCGACGCTCTG T C ECSIT Ensembl:ENSG00000130159 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs143156088 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_192614,RMVar_hsa_circ_113884 24520 RMVar_ID_24520 Human_SNP_ID_658523648 A-to-I Human chr19 - 11520467 11520467 11520467 ATGCATGAACCTTGAAAACACGTCAGTGGGCCAGGTGCGGTGGCTCACGCCTGTAATCCCAGCAC ATGCATGAACCTTGAAAACACGTCAGTGGGCCGGGTGCGGTGGCTCACGCCTGTAATCCCAGCAC T C ECSIT Ensembl:ENSG00000130159 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1450922995 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_192614,RMVar_hsa_circ_113884 24521 RMVar_ID_24521 Human_SNP_ID_658523649 A-to-I Human chr19 - 11520467 11520467 11520467 ATGCATGAACCTTGAAAACACGTCAGTGGGCCAGGTGCGGTGGCTCACGCCTGTAATCCCAGCAC ATGCATGAACCTTGAAAACACGTCAGTGGGCCCGGTGCGGTGGCTCACGCCTGTAATCCCAGCAC T G ECSIT Ensembl:ENSG00000130159 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1450922995 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_192614,RMVar_hsa_circ_113884 24522 RMVar_ID_24522 Human_SNP_ID_658525007 A-to-I Human chr19 - 11526192 11526192 11526192 TTGGGAGGCCAAGGCAGGTGGATCACAAGGTCAGGAGTTCAAGACCAGTCTGGACAAGATGGTGA TTGGGAGGCCAAGGCAGGTGGATCACAAGGTCGGGAGTTCAAGACCAGTCTGGACAAGATGGTGA T C ECSIT Ensembl:ENSG00000130159 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs557249245 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_192614,RMVar_hsa_circ_113884 24523 RMVar_ID_24523 Human_SNP_ID_658525158 A-to-I Human chr19 - 11526848 11526848 11526848 GGGTGTGGTGGCACACACCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCATGAGAACCAACTTGA GGGTGTGGTGGCACACACCTGTAGTCCCAGCTTCTCGGGAGGCTGAGGCATGAGAACCAACTTGA T A ECSIT Ensembl:ENSG00000130159 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1444506542 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_192614,RMVar_hsa_circ_113884 24524 RMVar_ID_24524 Human_SNP_ID_658525170 A-to-I Human chr19 - 11526899 11526899 11526899 CCTGAGCAACATGATGAAACCCCATCTCTACTAAAATACAAAAAATTAGCTGGGTGTGGTGGCAC CCTGAGCAACATGATGAAACCCCATCTCTACTGAAATACAAAAAATTAGCTGGGTGTGGTGGCAC T C ECSIT Ensembl:ENSG00000130159 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1178429817 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_192614,RMVar_hsa_circ_113884 24525 RMVar_ID_24525 Human_SNP_ID_658525194 A-to-I Human chr19 - 11526999 11526999 11526999 AAAGCTCCCTCTGGCTGGGTGTGGTGGCTCACACCTGTAATCCTAGCACTTTGGGAGGCCAAGAT AAAGCTCCCTCTGGCTGGGTGTGGTGGCTCACGCCTGTAATCCTAGCACTTTGGGAGGCCAAGAT T C ECSIT Ensembl:ENSG00000130159 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs930537093 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_192614,RMVar_hsa_circ_113884 24526 RMVar_ID_24526 Human_SNP_ID_658525259 A-to-I Human chr19 - 11527313 11527313 11527313 TTAGTTGATTTATTTATTTATTTAGCGATGGAATCTCGCTCTGTCGCCCAGACTGGGGTGCAGTG TTAGTTGATTTATTTATTTATTTAGCGATGGAGTCTCGCTCTGTCGCCCAGACTGGGGTGCAGTG T C ECSIT Ensembl:ENSG00000130159 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917690651 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_192614,RMVar_hsa_circ_113884 24527 RMVar_ID_24527 Human_SNP_ID_658525512 A-to-I Human chr19 - 11528444 11528444 11528444 CCCAGGAGTTTCGAGACCAGCCTTGGCAACATAGCAAGACCCTGTTCTCTACAAAAAATTATCTG CCCAGGAGTTTCGAGACCAGCCTTGGCAACATTGCAAGACCCTGTTCTCTACAAAAAATTATCTG T A ECSIT Ensembl:ENSG00000130159 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1018065978 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_192614,RMVar_hsa_circ_113884 24528 RMVar_ID_24528 Human_SNP_ID_658534227 A-to-I Human chr19 - 11558576 11558576 11558576 CAGACTCAAGGCTAATTTTTGTAATTTTGTAGAGATGAAGGGTCTCACTCTGTTTCCCAGGCTGG CAGACTCAAGGCTAATTTTTGTAATTTTGTAGCGATGAAGGGTCTCACTCTGTTTCCCAGGCTGG T G ELOF1 Ensembl:ENSG00000130165 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs936436975 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108045,RMVar_hsa_circ_192624,RMVar_hsa_circ_192625,RMVar_hsa_circ_98555 24529 RMVar_ID_24529 Human_SNP_ID_658534237 A-to-I Human chr19 - 11558631 11558631 11558631 CCTCGACCTCCTGGGCGCAAGCTTCCCACTTCAGCTTGCCGAGTAGCTGGGACTACAGACTCAAG CCTCGACCTCCTGGGCGCAAGCTTCCCACTTCGGCTTGCCGAGTAGCTGGGACTACAGACTCAAG T C ELOF1 Ensembl:ENSG00000130165 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1241209368 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108045,RMVar_hsa_circ_192624,RMVar_hsa_circ_192625,RMVar_hsa_circ_98555 24530 RMVar_ID_24530 Human_SNP_ID_658535525 A-to-I Human chr19 + 11563794 11563794 11563794 AGCTCAAGTGATCCACCCGCTTCTGCCTCCCAAAGTGCTGGGATTACAGGCCTGAGCCACCGCGC AGCTCAAGTGATCCACCCGCTTCTGCCTCCCATAGTGCTGGGATTACAGGCCTGAGCCACCGCGC A T ZNF627 Ensembl:ENSG00000198551 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs890367296 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75777,RMVar_hsa_circ_192627 24531 RMVar_ID_24531 Human_SNP_ID_658543036 A-to-I Human chr19 + 11590413 11590413 11590413 GCACCATCTGCTCACTGTGACCTCGACCTCTCAAGCTCAAGCGATCCTCCTACCTCAGCCTCCCC GCACCATCTGCTCACTGTGACCTCGACCTCTCGAGCTCAAGCGATCCTCCTACCTCAGCCTCCCC A G ZNF627 Ensembl:ENSG00000198551 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1242584082 Functional Loss SNV dbSNP153 33..33 33 - - - 24532 RMVar_ID_24532 Human_SNP_ID_658559814 A-to-I Human chr19 + 11655121 11655121 11655121 TGCTCTTGTTGCCTAGGCTGGAGCGCAATGGCACAATCTTGGCTCAATGCAACCTCCACCTCCTG TGCTCTTGTTGCCTAGGCTGGAGCGCAATGGCTCAATCTTGGCTCAATGCAACCTCCACCTCCTG A T AC008543.1 Ensembl:ENSG00000197332 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs970088626 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36434 24533 RMVar_ID_24533 Human_SNP_ID_658562316 A-to-I Human chr19 + 11665195 11665195 11665195 TATTTTTAGTAGAGACGGGGTTTCACCATGTTAGCCAGGATGGTCTCGATCTCCTGACCTCGTGA TATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGATGGTCTCGATCTCCTGACCTCGTGA A G AC008543.1 Ensembl:ENSG00000197332 lincRNA intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1485952068 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36434 24534 RMVar_ID_24534 Human_SNP_ID_658579306 A-to-I Human chr19 - 11731827 11731827 11731827 TTTTGCATTTTTAGTAGAGGTGGGGTTTCTCCATGTTGGCCAGGCAGGTCTCGAACTCCTGACCT TTTTGCATTTTTAGTAGAGGTGGGGTTTCTCCGTGTTGGCCAGGCAGGTCTCGAACTCCTGACCT T C ZNF823 Ensembl:ENSG00000197933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1416893580 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118333,RMVar_hsa_circ_192632 24535 RMVar_ID_24535 Human_SNP_ID_658579465 A-to-I Human chr19 - 11732303 11732303 11732303 AAAATTAGCTGGGCGTGGTGGCAGTTGCCTGTAGTCCCGGCTGCTCGGGAGGCTGAGGCAGGAGA AAAATTAGCTGGGCGTGGTGGCAGTTGCCTGTCGTCCCGGCTGCTCGGGAGGCTGAGGCAGGAGA T G ZNF823 Ensembl:ENSG00000197933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1282213342 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118333,RMVar_hsa_circ_192632 24536 RMVar_ID_24536 Human_SNP_ID_658597920 A-to-I Human chr19 + 11808134 11808134 11808134 AGCTGGGTGCAGTGGCTCATGCCTGTAACCCCAGCACTTTGGGAGGCCGAGGTGGGCGGATCACG AGCTGGGTGCAGTGGCTCATGCCTGTAACCCCGGCACTTTGGGAGGCCGAGGTGGGCGGATCACG A G ZNF491 Ensembl:ENSG00000177599 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs993520488 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269592 24537 RMVar_ID_24537 Human_SNP_ID_658600385 A-to-I Human chr19 + 11816828 11816828 11816828 AATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGTTCCTGAACTCCTGA AATTTTTGTATTTTTAGTAGAGATGGGGTTTCCCCATGTTGGCCAGGCTGTTCCTGAACTCCTGA A C ZNF440 Ensembl:ENSG00000171295 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1312325861 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120018,RMVar_hsa_circ_192643 24538 RMVar_ID_24538 Human_SNP_ID_658600386 A-to-I Human chr19 + 11816828 11816828 11816828 AATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGTTCCTGAACTCCTGA AATTTTTGTATTTTTAGTAGAGATGGGGTTTCGCCATGTTGGCCAGGCTGTTCCTGAACTCCTGA A G ZNF440 Ensembl:ENSG00000171295 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1312325861 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120018,RMVar_hsa_circ_192643 24539 RMVar_ID_24539 Human_SNP_ID_658600496 A-to-I Human chr19 + 11817345 11817345 11817345 TGGGCCAGCATGATGGCTTAGGCCTGTAATCTAAGCACTTTGGGAGGCCGAGGTGGGAGGATCAC TGGGCCAGCATGATGGCTTAGGCCTGTAATCTGAGCACTTTGGGAGGCCGAGGTGGGAGGATCAC A G ZNF440 Ensembl:ENSG00000171295 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971534734 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120018,RMVar_hsa_circ_192643 24540 RMVar_ID_24540 Human_SNP_ID_658601077 A-to-I Human chr19 + 11819538 11819538 11819538 CTCCTGCCTCAGCCTCCCAAGTATCTGGGATTACAGGTGCGTACCACCACACTTGGCTAATTTTT CTCCTGCCTCAGCCTCCCAAGTATCTGGGATTGCAGGTGCGTACCACCACACTTGGCTAATTTTT A G ZNF440 Ensembl:ENSG00000171295 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs535431132 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120018,RMVar_hsa_circ_192643 24541 RMVar_ID_24541 Human_SNP_ID_658601911 A-to-I Human chr19 + 11822740 11822740 11822740 GTGGTGGTACATGGCTGTAATCCCAGCTACTCAGGAGGCTGAAACAGGAGAATCACGAGAACCTG GTGGTGGTACATGGCTGTAATCCCAGCTACTCGGGAGGCTGAAACAGGAGAATCACGAGAACCTG A G ZNF440 Ensembl:ENSG00000171295 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1332457627 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120018,RMVar_hsa_circ_192643 24542 RMVar_ID_24542 Human_SNP_ID_658602210 A-to-I Human chr19 + 11823919 11823919 11823919 GGGAGTCCAAGGTTGCGGTAAGCCAAGATCACACCACTGCACTCCAGCCTGGGCAACAAGAGTGA GGGAGTCCAAGGTTGCGGTAAGCCAAGATCACGCCACTGCACTCCAGCCTGGGCAACAAGAGTGA A G ZNF440 Ensembl:ENSG00000171295 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs563751791 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120018,RMVar_hsa_circ_192643 24543 RMVar_ID_24543 Human_SNP_ID_658602258 A-to-I Human chr19 + 11824076 11824076 11824076 ATTGTGATGTGTGCCTGTCGTCCCAGCTACTCAGGAGGCTGAGGTAGAAGGATCTGTTGAGCCTA ATTGTGATGTGTGCCTGTCGTCCCAGCTACTCGGGAGGCTGAGGTAGAAGGATCTGTTGAGCCTA A G ZNF440 Ensembl:ENSG00000171295 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335616257 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120018,RMVar_hsa_circ_192643 24544 RMVar_ID_24544 Human_SNP_ID_658603092 A-to-I Human chr19 + 11826838 11826838 11826838 GGTGTATGCTGCCACACATGGCCACTGTTTGTATTATTAGTAGAGACAGAGTTTCACTGTGTTGG GGTGTATGCTGCCACACATGGCCACTGTTTGTGTTATTAGTAGAGACAGAGTTTCACTGTGTTGG A G ZNF440 Ensembl:ENSG00000171295 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1291283068 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13367383 RMVar_hsa_circ_120018,RMVar_hsa_circ_192643 24545 RMVar_ID_24545 Human_SNP_ID_658603778 A-to-I Human chr19 + 11829758 11829758 11829758 AGGAGGCTGAGGCATGAGAATTGCATGAACCCAGGAGTAAGAGGTTGTAGTGAGCCAAGATGGTG AGGAGGCTGAGGCATGAGAATTGCATGAACCCGGGAGTAAGAGGTTGTAGTGAGCCAAGATGGTG A G ZNF440 Ensembl:ENSG00000171295 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1236122659 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120018,RMVar_hsa_circ_192643 24546 RMVar_ID_24546 Human_SNP_ID_658603804 A-to-I Human chr19 + 11829886 11829886 11829886 CTGGGCATGGTGGCTCATGCCTGTAATCCCAGAACTTTGGGAGCCTGAGGCAGGCAGATCACCTG CTGGGCATGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGCCTGAGGCAGGCAGATCACCTG A C ZNF440 Ensembl:ENSG00000171295 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs959575531 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120018,RMVar_hsa_circ_192643 24547 RMVar_ID_24547 Human_SNP_ID_658603839 A-to-I Human chr19 + 11830015 11830015 11830015 ATGGTGGCATATGCCTGTAATCTTAGCTACTCAGGAGGCTGAGGAAGAAGAAGTGCTAGAACCCC ATGGTGGCATATGCCTGTAATCTTAGCTACTCGGGAGGCTGAGGAAGAAGAAGTGCTAGAACCCC A G ZNF440 Ensembl:ENSG00000171295 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs899103437 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120018,RMVar_hsa_circ_192643 24548 RMVar_ID_24548 Human_SNP_ID_658605269 A-to-I Human chr19 + 11834403 11834403 11834403 CCCACCTCGGCCTCCCAAAATGCTGGGATTACAGACATGAACCATCATGCCCAGCTGCAACCCTA CCCACCTCGGCCTCCCAAAATGCTGGGATTACGGACATGAACCATCATGCCCAGCTGCAACCCTA A G ZNF440 Ensembl:ENSG00000171295 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs548862984 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79330,RMVar_hsa_circ_192644 24549 RMVar_ID_24549 Human_SNP_ID_658605377 A-to-I Human chr19 + 11834851 11834851 11834851 CCCAGCACTTTGGGAGGCCGAGGTCAGGAGTTAGAGACCATTCTGACCAATATGATCAAACCCCG CCCAGCACTTTGGGAGGCCGAGGTCAGGAGTTGGAGACCATTCTGACCAATATGATCAAACCCCG A G ZNF440 Ensembl:ENSG00000171295 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1331058741 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79330,RMVar_hsa_circ_192644 24550 RMVar_ID_24550 Human_SNP_ID_658605386 A-to-I Human chr19 + 11834892 11834892 11834892 TCTGACCAATATGATCAAACCCCGTCTCTACTAAAAATACAAAAGTTAGCAGGGCGTGGTGGCAT TCTGACCAATATGATCAAACCCCGTCTCTACTGAAAATACAAAAGTTAGCAGGGCGTGGTGGCAT A G ZNF440 Ensembl:ENSG00000171295 Protein coding 3'UTR GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,31158229,31158229 RNA-Seq:(High) rs903003052 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79330,RMVar_hsa_circ_192644 24551 RMVar_ID_24551 Human_SNP_ID_658605449 A-to-I Human chr19 + 11835108 11835108 11835108 GGCCTTAGGGCCGAGTGCGGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCCGAGGCGGGC GGCCTTAGGGCCGAGTGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGC A G ZNF440 Ensembl:ENSG00000171295 Protein coding 3'UTR GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,31158229,32596459 RNA-Seq:(High) rs938129640 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79330,RMVar_hsa_circ_192644 24552 RMVar_ID_24552 Human_SNP_ID_658605473 A-to-I Human chr19 + 11835182 11835182 11835182 GGTCAGGAAATGGAGACCATCCTGGCCAACACAGTGAAACCCAGTCTCTACTAAAAAATACAAAA GGTCAGGAAATGGAGACCATCCTGGCCAACACCGTGAAACCCAGTCTCTACTAAAAAATACAAAA A C ZNF440 Ensembl:ENSG00000171295 Protein coding 3'UTR GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs888863257 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79330,RMVar_hsa_circ_192644 24553 RMVar_ID_24553 Human_SNP_ID_658605477 A-to-I Human chr19 + 11835199 11835199 11835199 CATCCTGGCCAACACAGTGAAACCCAGTCTCTACTAAAAAATACAAAAAATTAGTGAGGCGTGGT CATCCTGGCCAACACAGTGAAACCCAGTCTCTTCTAAAAAATACAAAAAATTAGTGAGGCGTGGT A T ZNF440 Ensembl:ENSG00000171295 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1227421058 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79330,RMVar_hsa_circ_192644 24554 RMVar_ID_24554 Human_SNP_ID_658625290 A-to-I Human chr19 + 11913450 11913449 11913451 TCACTCTGTCACCCAGGCTGGAGTGCAGTGGCATGATCTCAGGTCGCTGCAACCTCTGCCTCCAG TCACTCTGTCACCCAGGCTGGAGTGCAGTGGC__GATCTCAGGTCGCTGCAACCTCTGCCTCCAG CAT C ZNF69 Ensembl:ENSG00000198429 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1285162376 Functional Loss DEL dbSNP153 33..34 33 - - - Human_Splice_Rec_1961494 24555 RMVar_ID_24555 Human_SNP_ID_658625325 A-to-I Human chr19 + 11913571 11913571 11913571 CCACCACGCCAGGCTAATTTTTTGTATTTTTTAGTAGAGACAGGGTTTCACCATATTGGCCAGGC CCACCACGCCAGGCTAATTTTTTGTATTTTTTGGTAGAGACAGGGTTTCACCATATTGGCCAGGC A G ZNF69 Ensembl:ENSG00000198429 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs958621756 Functional Loss SNV dbSNP153 33..33 33 - - - 24556 RMVar_ID_24556 Human_SNP_ID_658625326 A-to-I Human chr19 + 11913574 11913574 11913574 CCACGCCAGGCTAATTTTTTGTATTTTTTAGTAGAGACAGGGTTTCACCATATTGGCCAGGCTGG CCACGCCAGGCTAATTTTTTGTATTTTTTAGTGGAGACAGGGTTTCACCATATTGGCCAGGCTGG A G ZNF69 Ensembl:ENSG00000198429 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1444161644 Functional Loss SNV dbSNP153 33..33 33 - - - 24557 RMVar_ID_24557 Human_SNP_ID_658625330 A-to-I Human chr19 + 11913580 11913580 11913580 CAGGCTAATTTTTTGTATTTTTTAGTAGAGACAGGGTTTCACCATATTGGCCAGGCTGGTCTTGA CAGGCTAATTTTTTGTATTTTTTAGTAGAGACGGGGTTTCACCATATTGGCCAGGCTGGTCTTGA A G ZNF69 Ensembl:ENSG00000198429 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs867532466 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_141230 24558 RMVar_ID_24558 Human_SNP_ID_658625465 A-to-I Human chr19 + 11914160 11914160 11914160 CAATATGATCAAACCCCGTCTCTACTAAAAATACAAAAATTAGCGGGGTGTGGTGGCATGCTCCT CAATATGATCAAACCCCGTCTCTACTAAAAATGCAAAAATTAGCGGGGTGTGGTGGCATGCTCCT A G ZNF69 Ensembl:ENSG00000198429 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs556974864 Functional Loss SNV dbSNP153 33..33 33 - - - 24559 RMVar_ID_24559 Human_SNP_ID_658628874 A-to-I Human chr19 + 11927286 11927286 11927286 TGATGTGAGAGAATCACTTGAACCCCAGAGGCAGAGGTTGCAGCCCAGCCGAGGATGTACCACTG TGATGTGAGAGAATCACTTGAACCCCAGAGGCGGAGGTTGCAGCCCAGCCGAGGATGTACCACTG A G AC008770.2,ZNF700 Ensembl:ENSG00000267179,Ensembl:ENSG00000196757 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs960910899 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23310093 RMVar_hsa_circ_97726,RMVar_hsa_circ_125943,RMVar_hsa_circ_92767,RMVar_hsa_circ_192645,RMVar_hsa_circ_113611,RMVar_hsa_circ_192647,RMVar_hsa_circ_192648,RMVar_hsa_circ_192646 24560 RMVar_ID_24560 Human_SNP_ID_658629098 A-to-I Human chr19 + 11928046 11928046 11928046 TTGAGACAGTATCTTGCTCTGTGACCCAGCCTAGAGCAGTGGTGCGATGATGGCTTACTGCAGCC TTGAGACAGTATCTTGCTCTGTGACCCAGCCTCGAGCAGTGGTGCGATGATGGCTTACTGCAGCC A C AC008770.2,ZNF700 Ensembl:ENSG00000267179,Ensembl:ENSG00000196757 Protein coding,Protein coding intron,intron GSE38233;GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1019695689 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23782157 RMVar_hsa_circ_97726,RMVar_hsa_circ_125943,RMVar_hsa_circ_92767,RMVar_hsa_circ_192645,RMVar_hsa_circ_113611,RMVar_hsa_circ_192647,RMVar_hsa_circ_192648,RMVar_hsa_circ_192646 24561 RMVar_ID_24561 Human_SNP_ID_658629401 A-to-I Human chr19 + 11929189 11929189 11929189 TACTTTGTTGTTTTTGTTGTTTGTTTTGAGATAGGGTCTCACTCTGTCACCCAGGCTGGAGTGCA TACTTTGTTGTTTTTGTTGTTTGTTTTGAGATGGGGTCTCACTCTGTCACCCAGGCTGGAGTGCA A G AC008770.2,ZNF700 Ensembl:ENSG00000267179,Ensembl:ENSG00000196757 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs748798239 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97726,RMVar_hsa_circ_125943,RMVar_hsa_circ_92767,RMVar_hsa_circ_192645,RMVar_hsa_circ_113611,RMVar_hsa_circ_192647,RMVar_hsa_circ_192648,RMVar_hsa_circ_192646 24562 RMVar_ID_24562 Human_SNP_ID_658629434 A-to-I Human chr19 + 11929338 11929338 11929338 GACATGTGCCACCACACTCAGCTGATTTTTGTATTTTTAGTAAAGACAGGGTTTTACCACACTGG GACATGTGCCACCACACTCAGCTGATTTTTGTGTTTTTAGTAAAGACAGGGTTTTACCACACTGG A G AC008770.2,ZNF700 Ensembl:ENSG00000267179,Ensembl:ENSG00000196757 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1195714636 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13367475 RMVar_hsa_circ_97726,RMVar_hsa_circ_125943,RMVar_hsa_circ_92767,RMVar_hsa_circ_192645,RMVar_hsa_circ_113611,RMVar_hsa_circ_192647,RMVar_hsa_circ_192648,RMVar_hsa_circ_192646 24563 RMVar_ID_24563 Human_SNP_ID_658629748 A-to-I Human chr19 + 11930878 11930878 11930878 AAAATTAGCCAAGCATAGTGGTGCATGGCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTAGCCAAGCATAGTGGTGCATGGCTGTGATCCCAGCTACTCGGGAGGCTGAGGCAGGAGA A G AC008770.2,ZNF700 Ensembl:ENSG00000267179,Ensembl:ENSG00000196757 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs548744190 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97726,RMVar_hsa_circ_125943,RMVar_hsa_circ_92767,RMVar_hsa_circ_192645,RMVar_hsa_circ_113611,RMVar_hsa_circ_192647,RMVar_hsa_circ_192648,RMVar_hsa_circ_192646 24564 RMVar_ID_24564 Human_SNP_ID_658629997 A-to-I Human chr19 + 11931858 11931858 11931858 AAATTAGTGGCCAGGCACGGTGGCTCGCGCCTATAATCCCAACACTTTAGGAGGTCAATGCATGC AAATTAGTGGCCAGGCACGGTGGCTCGCGCCTGTAATCCCAACACTTTAGGAGGTCAATGCATGC A G AC008770.2,ZNF700 Ensembl:ENSG00000267179,Ensembl:ENSG00000196757 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1411285820 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97726,RMVar_hsa_circ_125943,RMVar_hsa_circ_92767,RMVar_hsa_circ_192645,RMVar_hsa_circ_113611,RMVar_hsa_circ_192647,RMVar_hsa_circ_192648,RMVar_hsa_circ_192646 24565 RMVar_ID_24565 Human_SNP_ID_658630089 A-to-I Human chr19 + 11932223 11932223 11932223 AAACTTACCTGGTCATGGTGATGTGCGCCTGTAGACCCAGCTACTCAGGAGACTGAGGTGGAAGG AAACTTACCTGGTCATGGTGATGTGCGCCTGTGGACCCAGCTACTCAGGAGACTGAGGTGGAAGG A G AC008770.2,ZNF700 Ensembl:ENSG00000267179,Ensembl:ENSG00000196757 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1473370080 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17568464 RMVar_hsa_circ_97726,RMVar_hsa_circ_125943,RMVar_hsa_circ_92767,RMVar_hsa_circ_192645,RMVar_hsa_circ_113611,RMVar_hsa_circ_192647,RMVar_hsa_circ_192648,RMVar_hsa_circ_192646 24566 RMVar_ID_24566 Human_SNP_ID_658630093 A-to-I Human chr19 + 11932269 11932269 11932269 AGGAGACTGAGGTGGAAGGATCTGTTGAGCCTAGGAGTTCAAGGCTGCAGTGAGCTATGATTGCA AGGAGACTGAGGTGGAAGGATCTGTTGAGCCTGGGAGTTCAAGGCTGCAGTGAGCTATGATTGCA A G AC008770.2,ZNF700 Ensembl:ENSG00000267179,Ensembl:ENSG00000196757 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1400442575 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97726,RMVar_hsa_circ_125943,RMVar_hsa_circ_92767,RMVar_hsa_circ_192645,RMVar_hsa_circ_113611,RMVar_hsa_circ_192647,RMVar_hsa_circ_192648,RMVar_hsa_circ_192646 24567 RMVar_ID_24567 Human_SNP_ID_658630238 A-to-I Human chr19 + 11932767 11932767 11932767 TCACGCCATTCTCCTGTCTCAGCCTCCCAAGTAGCTGGGACTACAGGCACCCGCCACCCCGTCCG TCACGCCATTCTCCTGTCTCAGCCTCCCAAGTTGCTGGGACTACAGGCACCCGCCACCCCGTCCG A T AC008770.2,ZNF700 Ensembl:ENSG00000267179,Ensembl:ENSG00000196757 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1460763800 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97726,RMVar_hsa_circ_125943,RMVar_hsa_circ_92767,RMVar_hsa_circ_192645,RMVar_hsa_circ_113611,RMVar_hsa_circ_192647,RMVar_hsa_circ_192648,RMVar_hsa_circ_192646 24568 RMVar_ID_24568 Human_SNP_ID_658630321 A-to-I Human chr19 + 11933140 11933140 11933140 AGTTCCCCCTATTTTAAACATCTTGACTGGCCAGGTGCTGTGCCTCATACCTGTAATTCTACCAC AGTTCCCCCTATTTTAAACATCTTGACTGGCCGGGTGCTGTGCCTCATACCTGTAATTCTACCAC A G AC008770.2,ZNF700 Ensembl:ENSG00000267179,Ensembl:ENSG00000196757 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs534473772 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13367523 RMVar_hsa_circ_97726,RMVar_hsa_circ_125943,RMVar_hsa_circ_92767,RMVar_hsa_circ_192645,RMVar_hsa_circ_113611,RMVar_hsa_circ_192647,RMVar_hsa_circ_192648,RMVar_hsa_circ_192646 24569 RMVar_ID_24569 Human_SNP_ID_658630772 A-to-I Human chr19 + 11934947 11934947 11934947 TCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGTGGATCAGGAGGTCAGATCAAGACC TCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGTGGATCAGGAGGTCAGATCAAGACC A G AC008770.2,ZNF700 Ensembl:ENSG00000267179,Ensembl:ENSG00000196757 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs279241 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97726,RMVar_hsa_circ_125943,RMVar_hsa_circ_92767,RMVar_hsa_circ_192645,RMVar_hsa_circ_113611,RMVar_hsa_circ_192647,RMVar_hsa_circ_192648,RMVar_hsa_circ_192646 24570 RMVar_ID_24570 Human_SNP_ID_658630969 A-to-I Human chr19 + 11935336 11935336 11935336 TCGGCTCACTGCAACATCTGCCTCCCAGGTTCAAGTGATTCATCTGCCTCAGCCTCCAGAGTAGG TCGGCTCACTGCAACATCTGCCTCCCAGGTTCCAGTGATTCATCTGCCTCAGCCTCCAGAGTAGG A C AC008770.2,ZNF700 Ensembl:ENSG00000267179,Ensembl:ENSG00000196757 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs868049152 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97726,RMVar_hsa_circ_125943,RMVar_hsa_circ_92767,RMVar_hsa_circ_192645,RMVar_hsa_circ_113611,RMVar_hsa_circ_192647,RMVar_hsa_circ_192648,RMVar_hsa_circ_192646 24571 RMVar_ID_24571 Human_SNP_ID_658630972 A-to-I Human chr19 + 11935341 11935341 11935341 TCACTGCAACATCTGCCTCCCAGGTTCAAGTGATTCATCTGCCTCAGCCTCCAGAGTAGGTGGGA TCACTGCAACATCTGCCTCCCAGGTTCAAGTGTTTCATCTGCCTCAGCCTCCAGAGTAGGTGGGA A T AC008770.2,ZNF700 Ensembl:ENSG00000267179,Ensembl:ENSG00000196757 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs921260698 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17568466 RMVar_hsa_circ_97726,RMVar_hsa_circ_125943,RMVar_hsa_circ_92767,RMVar_hsa_circ_192645,RMVar_hsa_circ_113611,RMVar_hsa_circ_192647,RMVar_hsa_circ_192648,RMVar_hsa_circ_192646 24572 RMVar_ID_24572 Human_SNP_ID_658630986 A-to-I Human chr19 + 11935417 11935417 11935417 CACCACCAGGCCCAACTAATTTTTGTATTTTTAGTTGAGACTGGGTTTCACCATGTTAGGCTGAT CACCACCAGGCCCAACTAATTTTTGTATTTTTCGTTGAGACTGGGTTTCACCATGTTAGGCTGAT A C AC008770.2,ZNF700 Ensembl:ENSG00000267179,Ensembl:ENSG00000196757 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1198185002 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13367577 RMVar_hsa_circ_97726,RMVar_hsa_circ_125943,RMVar_hsa_circ_92767,RMVar_hsa_circ_192645,RMVar_hsa_circ_113611,RMVar_hsa_circ_192647,RMVar_hsa_circ_192648,RMVar_hsa_circ_192646 24573 RMVar_ID_24573 Human_SNP_ID_658631610 A-to-I Human chr19 + 11937628 11937628 11937628 CTCCTGCCTCAGCCTCCCGAGTAACTGAGACTACAGGTGCCTACCACCACGCTTGGCTAATTTTT CTCCTGCCTCAGCCTCCCGAGTAACTGAGACTGCAGGTGCCTACCACCACGCTTGGCTAATTTTT A G AC008770.2,ZNF700 Ensembl:ENSG00000267179,Ensembl:ENSG00000196757 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1476529345 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97726,RMVar_hsa_circ_125943,RMVar_hsa_circ_92767,RMVar_hsa_circ_192645,RMVar_hsa_circ_113611,RMVar_hsa_circ_192647,RMVar_hsa_circ_192648,RMVar_hsa_circ_192646 24574 RMVar_ID_24574 Human_SNP_ID_658632118 A-to-I Human chr19 + 11939626 11939626 11939626 TTGGTACCAGTACCATGCTGTTGCGCCTGGCTAATTTTTGTATTTTTAGTAGAGATGGAGTTCCA TTGGTACCAGTACCATGCTGTTGCGCCTGGCTGATTTTTGTATTTTTAGTAGAGATGGAGTTCCA A G AC008770.2,ZNF700 Ensembl:ENSG00000267179,Ensembl:ENSG00000196757 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1214667763 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13367623 RMVar_hsa_circ_97726,RMVar_hsa_circ_125943,RMVar_hsa_circ_92767,RMVar_hsa_circ_192645,RMVar_hsa_circ_113611,RMVar_hsa_circ_192647,RMVar_hsa_circ_192648,RMVar_hsa_circ_192646 24575 RMVar_ID_24575 Human_SNP_ID_658633958 A-to-I Human chr19 + 11946877 11946877 11946877 TAAAGGTCACTCACGCGTGGTGGTACATGCCTATAATCCCAGCTACTCGGGAGGCTGAGGCAGGA TAAAGGTCACTCACGCGTGGTGGTACATGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGA A G AC008770.3,AC008770.2,ZNF700 Ensembl:ENSG00000267274,Ensembl:ENSG00000267179,Ensembl:ENSG00000196757 lincRNA,Protein coding,Protein coding intron,intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1168008387 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97726,RMVar_hsa_circ_125943,RMVar_hsa_circ_92767,RMVar_hsa_circ_192645,RMVar_hsa_circ_113611,RMVar_hsa_circ_192647,RMVar_hsa_circ_192648,RMVar_hsa_circ_192646 24576 RMVar_ID_24576 Human_SNP_ID_658633961 A-to-I Human chr19 + 11946889 11946889 11946889 ACGCGTGGTGGTACATGCCTATAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAA ACGCGTGGTGGTACATGCCTATAATCCCAGCTGCTCGGGAGGCTGAGGCAGGAGAATCGCTTGAA A G AC008770.3,AC008770.2,ZNF700 Ensembl:ENSG00000267274,Ensembl:ENSG00000267179,Ensembl:ENSG00000196757 lincRNA,Protein coding,Protein coding intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs905401287 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97726,RMVar_hsa_circ_125943,RMVar_hsa_circ_92767,RMVar_hsa_circ_192645,RMVar_hsa_circ_113611,RMVar_hsa_circ_192647,RMVar_hsa_circ_192648,RMVar_hsa_circ_192646 24577 RMVar_ID_24577 Human_SNP_ID_658637016 A-to-I Human chr19 + 11956811 11956811 11956811 TCGGGGCGGAGGCTGCAGTGAGCCAAGATCACACCATTGCACTTCAGATTGGATGACTGAGCAAG TCGGGGCGGAGGCTGCAGTGAGCCAAGATCACGCCATTGCACTTCAGATTGGATGACTGAGCAAG A G AC008770.2 Ensembl:ENSG00000267179 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs943853191 Functional Loss SNV dbSNP153 33..33 33 - - - 24578 RMVar_ID_24578 Human_SNP_ID_658669827 A-to-I Human chr19 + 12078329 12078329 12078329 TTATATTTTTAGTAGAGATGAGGTCTCACCCTATTGGCCACACTGGTCTTGAACTCCTGACCTGA TTATATTTTTAGTAGAGATGAGGTCTCACCCTCTTGGCCACACTGGTCTTGAACTCCTGACCTGA A C AC022415.3,ZNF844 Ensembl:ENSG00000286132,Ensembl:ENSG00000223547 Protein coding,Protein coding intron,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs73514867 Functional Loss SNV dbSNP153 33..33 33 - - - 24579 RMVar_ID_24579 Human_SNP_ID_658669828 A-to-I Human chr19 + 12078329 12078329 12078329 TTATATTTTTAGTAGAGATGAGGTCTCACCCTATTGGCCACACTGGTCTTGAACTCCTGACCTGA TTATATTTTTAGTAGAGATGAGGTCTCACCCTGTTGGCCACACTGGTCTTGAACTCCTGACCTGA A G AC022415.3,ZNF844 Ensembl:ENSG00000286132,Ensembl:ENSG00000223547 Protein coding,Protein coding intron,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs73514867 Functional Loss SNV dbSNP153 33..33 33 - - - 24580 RMVar_ID_24580 Human_SNP_ID_658669829 A-to-I Human chr19 + 12078329 12078329 12078329 TTATATTTTTAGTAGAGATGAGGTCTCACCCTATTGGCCACACTGGTCTTGAACTCCTGACCTGA TTATATTTTTAGTAGAGATGAGGTCTCACCCTTTTGGCCACACTGGTCTTGAACTCCTGACCTGA A T AC022415.3,ZNF844 Ensembl:ENSG00000286132,Ensembl:ENSG00000223547 Protein coding,Protein coding intron,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs73514867 Functional Loss SNV dbSNP153 33..33 33 - - - 24581 RMVar_ID_24581 Human_SNP_ID_658669985 A-to-I Human chr19 + 12079033 12079033 12079033 CACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGCTTCACTATGTTGGCCAGGTTCG CACCACGCCCAGCTAATTTTTGTATTTTTAGTGGAGACGGGGCTTCACTATGTTGGCCAGGTTCG A G AC022415.3,ZNF844 Ensembl:ENSG00000286132,Ensembl:ENSG00000223547 Protein coding,Protein coding intron,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1201953864 Functional Loss SNV dbSNP153 33..33 33 - - - 24582 RMVar_ID_24582 Human_SNP_ID_658670093 A-to-I Human chr19 + 12079515 12079515 12079515 CCCTGTCTCTACCAAAAATACAAAAATTAGCCAGGCATGGTGGCGCGTGCCTGTAGTCCCAGCTA CCCTGTCTCTACCAAAAATACAAAAATTAGCCGGGCATGGTGGCGCGTGCCTGTAGTCCCAGCTA A G AC022415.3,ZNF844 Ensembl:ENSG00000286132,Ensembl:ENSG00000223547 Protein coding,Protein coding intron,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1162524977 Functional Loss SNV dbSNP153 33..33 33 - - - 24583 RMVar_ID_24583 Human_SNP_ID_658670094 A-to-I Human chr19 + 12079515 12079515 12079515 CCCTGTCTCTACCAAAAATACAAAAATTAGCCAGGCATGGTGGCGCGTGCCTGTAGTCCCAGCTA CCCTGTCTCTACCAAAAATACAAAAATTAGCCTGGCATGGTGGCGCGTGCCTGTAGTCCCAGCTA A T AC022415.3,ZNF844 Ensembl:ENSG00000286132,Ensembl:ENSG00000223547 Protein coding,Protein coding intron,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1162524977 Functional Loss SNV dbSNP153 33..33 33 - - - 24584 RMVar_ID_24584 Human_SNP_ID_658670102 A-to-I Human chr19 + 12079537 12079537 12079537 AAAATTAGCCAGGCATGGTGGCGCGTGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGA AAAATTAGCCAGGCATGGTGGCGCGTGCCTGTGGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGA A G AC022415.3,ZNF844 Ensembl:ENSG00000286132,Ensembl:ENSG00000223547 Protein coding,Protein coding intron,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1264218043 Functional Loss SNV dbSNP153 33..33 33 - - - 24585 RMVar_ID_24585 Human_SNP_ID_658670183 A-to-I Human chr19 + 12079895 12079895 12079895 TTGAACCTGGGAGGCGGAGGTTGCAGTGAGCCAAGATCACAGCATTGCACTTCAGCCTGGGCAAC TTGAACCTGGGAGGCGGAGGTTGCAGTGAGCCGAGATCACAGCATTGCACTTCAGCCTGGGCAAC A G AC022415.3,ZNF844 Ensembl:ENSG00000286132,Ensembl:ENSG00000223547 Protein coding,Protein coding intron,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs545092823 Functional Loss SNV dbSNP153 33..33 33 - - - 24586 RMVar_ID_24586 Human_SNP_ID_658670510 A-to-I Human chr19 + 12080887 12080887 12080887 GTGATTCTGGTGTCTCAGCCACCTGAGTAGTCAGGATTACAGGTGCACACCACCACGCATGGCTA GTGATTCTGGTGTCTCAGCCACCTGAGTAGTCGGGATTACAGGTGCACACCACCACGCATGGCTA A G AC022415.3,ZNF844 Ensembl:ENSG00000286132,Ensembl:ENSG00000223547 Protein coding,Protein coding intron,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1367512967 Functional Loss SNV dbSNP153 33..33 33 - - - 24587 RMVar_ID_24587 Human_SNP_ID_658670525 A-to-I Human chr19 + 12080955 12080954 12080955 TTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGAGCAAGCTGGTCTTAAACTCCTGACCT TTTTGTATTTTTAGTAGAGATGGGGTTTCACC_TGTTGAGCAAGCTGGTCTTAAACTCCTGACCT CA C AC022415.3,ZNF844 Ensembl:ENSG00000286132,Ensembl:ENSG00000223547 Protein coding,Protein coding intron,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs771757169 Functional Loss DEL dbSNP153 33..33 33 - - - 24588 RMVar_ID_24588 Human_SNP_ID_658670546 A-to-I Human chr19 + 12081029 12081029 12081029 CGTCTGTCTTGGCCTTTCAAAATGCTGGGATTATAGGCGTGATCCACTGTGCCTGGCCTGGTGTT CGTCTGTCTTGGCCTTTCAAAATGCTGGGATTGTAGGCGTGATCCACTGTGCCTGGCCTGGTGTT A G AC022415.3,ZNF844 Ensembl:ENSG00000286132,Ensembl:ENSG00000223547 Protein coding,Protein coding intron,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1000260636 Functional Loss SNV dbSNP153 33..33 33 - - - 24589 RMVar_ID_24589 Human_SNP_ID_658678794 A-to-I Human chr19 + 12113726 12113726 12113726 AAGAGACACATTCTGTTAATATGCATTCAGTTATCCTAATTCCTTTGAAACACAGAAAAAGAGTA AAGAGACACATTCTGTTAATATGCATTCAGTTTTCCTAATTCCTTTGAAACACAGAAAAAGAGTA A T ZNF788P Ensembl:ENSG00000214189 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs772325694 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103733,RMVar_hsa_circ_192654 24590 RMVar_ID_24590 Human_SNP_ID_658678943 A-to-I Human chr19 + 12114345 12114345 12114345 AAATCACTTGACTTTCCTTTTCTCAGAGTTATAGTTCTCCAGAGATGTCACCAGATGATTCACAT AAATCACTTGACTTTCCTTTTCTCAGAGTTATCGTTCTCCAGAGATGTCACCAGATGATTCACAT A C ZNF788P Ensembl:ENSG00000214189 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1260640850 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103733,RMVar_hsa_circ_192654 24591 RMVar_ID_24591 Human_SNP_ID_658687081 A-to-I Human chr19 - 12144987 12144987 12144987 AGGTTTGGCCGGGTGCAGTGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCCGAGGCAGGCGG AGGTTTGGCCGGGTGCAGTGGCTCATGCCTATCATCCCAGCACTTTGGGAGGCCGAGGCAGGCGG T G ZNF625,ZNF625-ZNF20 Ensembl:ENSG00000257591,Ensembl:ENSG00000213297 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1317568165 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69340,RMVar_hsa_circ_307583,RMVar_hsa_circ_323674 24592 RMVar_ID_24592 Human_SNP_ID_658687082 A-to-I Human chr19 - 12144989 12144989 12144989 CGAGGTTTGGCCGGGTGCAGTGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCCGAGGCAGGC CGAGGTTTGGCCGGGTGCAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGC T C ZNF625,ZNF625-ZNF20 Ensembl:ENSG00000257591,Ensembl:ENSG00000213297 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs201964757 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69340,RMVar_hsa_circ_307583,RMVar_hsa_circ_323674 24593 RMVar_ID_24593 Human_SNP_ID_658695843 A-to-I Human chr19 + 12177420 12177420 12177420 GCTGAAGTGCAGTGGCGCGATCTCGGCTCACTACAACCTCTACCTCCCGGGTCCCAGTTCAAGCA GCTGAAGTGCAGTGGCGCGATCTCGGCTCACTGCAACCTCTACCTCCCGGGTCCCAGTTCAAGCA A G ZNF136 Ensembl:ENSG00000196646 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879697027 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_192657 24594 RMVar_ID_24594 Human_SNP_ID_658699209 A-to-I Human chr19 + 12189965 12189961 12189965 CATTTCTTTCTTTCTTTCTGAAATAGGGTCTCACTCTGTCACTCAGGCTGGAGTGCAGTGGCACG CATTTCTTTCTTTCTTTCTGAAATAGGGT____CTCTGTCACTCAGGCTGGAGTGCAGTGGCACG TCTCA T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs990992934 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_3562926,Human_RBP_ID_20354216 24595 RMVar_ID_24595 Human_SNP_ID_658699616 A-to-I Human chr19 + 12191691 12191691 12191691 TAATCCCAGCATTTTGGGAGGCCAATGCGGGCAGATCACTTGAGGCCAGGAATTGGAGACCAGCC TAATCCCAGCATTTTGGGAGGCCAATGCGGGCGGATCACTTGAGGCCAGGAATTGGAGACCAGCC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913984502 Functional Loss SNV dbSNP153 33..33 33 - - - 24596 RMVar_ID_24596 Human_SNP_ID_658699620 A-to-I Human chr19 + 12191709 12191709 12191709 AGGCCAATGCGGGCAGATCACTTGAGGCCAGGAATTGGAGACCAGCCTGGACAACATAGCAACAC AGGCCAATGCGGGCAGATCACTTGAGGCCAGGTATTGGAGACCAGCCTGGACAACATAGCAACAC A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1007492512 Functional Loss SNV dbSNP153 33..33 33 - - - 24597 RMVar_ID_24597 Human_SNP_ID_658699819 A-to-I Human chr19 + 12192397 12192396 12192398 AGTAATTCTTTTTTTTTTTTCTTTTGTGAGACAGAGTCTTGCTCTGTTGCCCAGGCTGGAGTTCA AGTAATTCTTTTTTTTTTTTCTTTTGTGAGAC__AGTCTTGCTCTGTTGCCCAGGCTGGAGTTCA CAG C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1259056378 Functional Loss DEL dbSNP153 33..34 33 - - - 24598 RMVar_ID_24598 Human_SNP_ID_658699820 A-to-I Human chr19 + 12192397 12192397 12192397 AGTAATTCTTTTTTTTTTTTCTTTTGTGAGACAGAGTCTTGCTCTGTTGCCCAGGCTGGAGTTCA AGTAATTCTTTTTTTTTTTTCTTTTGTGAGACGGAGTCTTGCTCTGTTGCCCAGGCTGGAGTTCA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1237559319 Functional Loss SNV dbSNP153 33..33 33 - - - 24599 RMVar_ID_24599 Human_SNP_ID_658700131 A-to-I Human chr19 + 12193676 12193676 12193676 CCGTCTCAAACAAGAAAAAAAGAAAATGTTCTAGGCCAGGTGCCGTGGCTCATGCCTGTAATCCC CCGTCTCAAACAAGAAAAAAAGAAAATGTTCTGGGCCAGGTGCCGTGGCTCATGCCTGTAATCCC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1465121568 Functional Loss SNV dbSNP153 33..33 33 - - - 24600 RMVar_ID_24600 Human_SNP_ID_658700175 A-to-I Human chr19 + 12193836 12193836 12193836 CAAAAATCAGCCAAGCACAGTGGCGCGCGCCTATAATCCCAGCTACTCTGGAGGCTGAGGCAGAA CAAAAATCAGCCAAGCACAGTGGCGCGCGCCTGTAATCCCAGCTACTCTGGAGGCTGAGGCAGAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs895954816 Functional Loss SNV dbSNP153 33..33 33 - - - 24601 RMVar_ID_24601 Human_SNP_ID_658700181 A-to-I Human chr19 + 12193879 12193879 12193879 TACTCTGGAGGCTGAGGCAGAAGAATCGCTTGAACACCAGAATCGGAGGCTGTAGTGACCCGAGA TACTCTGGAGGCTGAGGCAGAAGAATCGCTTGCACACCAGAATCGGAGGCTGTAGTGACCCGAGA A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs967640968 Functional Loss SNV dbSNP153 33..33 33 - - - 24602 RMVar_ID_24602 Human_SNP_ID_658709159 A-to-I Human chr19 + 12232989 12232989 12232989 ATTGACAGAGCAAGAGCATCGCCATCGTGGACAAGCACCTCATTTTAAAATTCACCTTAATCAAA ATTGACAGAGCAAGAGCATCGCCATCGTGGACGAGCACCTCATTTTAAAATTCACCTTAATCAAA A G AC012618.3 Ensembl:ENSG00000234773 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1184577389 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_192659 24603 RMVar_ID_24603 Human_SNP_ID_658710460 A-to-I Human chr19 + 12238256 12238256 12238256 CTCACCCTATAATCCCAGCACTTTGGGAGGCCAAGGTAGGAGGATCACCTGAGGTCAGGAGTTTG CTCACCCTATAATCCCAGCACTTTGGGAGGCCGAGGTAGGAGGATCACCTGAGGTCAGGAGTTTG A G LOC100289333,LOC100289333:2,lnc-ZNF136-1,LOC100289333:3 RNACentral:URS00008B3D03,RNACentral:URS00008BE702,RNACentral:URS00008B5221,RNACentral:URS00008BE083 lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1369432968 Functional Loss SNV dbSNP153 33..33 33 - - - 24604 RMVar_ID_24604 Human_SNP_ID_658711680 A-to-I Human chr19 + 12242718 12242718 12242718 AAATATGATTTAAAAAATTACCTGGGCATGGTAGTGTGCACCTGTAGTCCCAGCTATTCAGGAGG AAATATGATTTAAAAAATTACCTGGGCATGGTCGTGTGCACCTGTAGTCCCAGCTATTCAGGAGG A C lnc-ZNF136-2,LOC100289333 RNACentral:URS0000D5B7FB,RNACentral:URS00008BE083 lincRNA,lincRNA exon,intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs562932448 Functional Loss SNV dbSNP153 33..33 33 - - - 24605 RMVar_ID_24605 Human_SNP_ID_658711681 A-to-I Human chr19 + 12242718 12242718 12242718 AAATATGATTTAAAAAATTACCTGGGCATGGTAGTGTGCACCTGTAGTCCCAGCTATTCAGGAGG AAATATGATTTAAAAAATTACCTGGGCATGGTGGTGTGCACCTGTAGTCCCAGCTATTCAGGAGG A G lnc-ZNF136-2,LOC100289333 RNACentral:URS0000D5B7FB,RNACentral:URS00008BE083 lincRNA,lincRNA exon,intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs562932448 Functional Loss SNV dbSNP153 33..33 33 - - - 24606 RMVar_ID_24606 Human_SNP_ID_658722177 A-to-I Human chr19 - 12283831 12283831 12283831 TTTTTTAATTTTGTGTAGCCAGAGGGTCTGCCATGTTGCCGGGCTGGTTTCAAATTCCTGGCCTC TTTTTTAATTTTGTGTAGCCAGAGGGTCTGCCGTGTTGCCGGGCTGGTTTCAAATTCCTGGCCTC T C ZNF44 Ensembl:ENSG00000197857 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1381555719 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17567958 24607 RMVar_ID_24607 Human_SNP_ID_658722185 A-to-I Human chr19 - 12283891 12283891 12283891 TCAAACTCCTGGGCTCCCAAGTAGCTGGGACTATAGGCATGTGCCACCACACTTGGCTAATTTTT TCAAACTCCTGGGCTCCCAAGTAGCTGGGACTGTAGGCATGTGCCACCACACTTGGCTAATTTTT T C ZNF44 Ensembl:ENSG00000197857 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs915265613 Functional Loss SNV dbSNP153 33..33 33 - - - 24608 RMVar_ID_24608 Human_SNP_ID_658722839 A-to-I Human chr19 - 12286512 12286512 12286512 TTTCTGCCTCAGCCTCCCGAGCAGCTAGGACTACAGGCACCCGCCACCACGCCCGGCTAATTTTT TTTCTGCCTCAGCCTCCCGAGCAGCTAGGACTGCAGGCACCCGCCACCACGCCCGGCTAATTTTT T C ZNF44 Ensembl:ENSG00000197857 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs944990190 Functional Loss SNV dbSNP153 33..33 33 - - - 24609 RMVar_ID_24609 Human_SNP_ID_658723311 A-to-I Human chr19 - 12288509 12288509 12288509 TCAAACTTCTGACCTCATTATTTGCCTACCTCAGCCTCCCAAAGTGCTGGGATTATAGGTGTGAG TCAAACTTCTGACCTCATTATTTGCCTACCTCGGCCTCCCAAAGTGCTGGGATTATAGGTGTGAG T C ZNF44 Ensembl:ENSG00000197857 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1470904862 Functional Loss SNV dbSNP153 33..33 33 - - - 24610 RMVar_ID_24610 Human_SNP_ID_658723560 A-to-I Human chr19 - 12289256 12289256 12289256 TTGCTCAGACTAGAGTGCAGTGGGGCCATCACAGCTCACTGCAGCCTTGACCTCCCCAGGCTGAG TTGCTCAGACTAGAGTGCAGTGGGGCCATCACGGCTCACTGCAGCCTTGACCTCCCCAGGCTGAG T C ZNF44 Ensembl:ENSG00000197857 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs768730911 Functional Loss SNV dbSNP153 33..33 33 - - - 24611 RMVar_ID_24611 Human_SNP_ID_658779088 A-to-I Human chr19 - 12501933 12501933 12501933 CATAACAACCCTAAACACTGAATTCCCAGGCCAGGCGCAGTGGCTCACACCTGTAATCCCAGCAT CATAACAACCCTAAACACTGAATTCCCAGGCCGGGCGCAGTGGCTCACACCTGTAATCCCAGCAT T C AC008758.1,ZNF709 Ensembl:ENSG00000196826,Ensembl:ENSG00000242852 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973093814 Functional Loss SNV dbSNP153 33..33 33 - - - 24612 RMVar_ID_24612 Human_SNP_ID_658784063 A-to-I Human chr19 - 12520495 12520495 12520495 ACGATCTTGGCTCACTGCAGCCTCCGCCTGTCAGGTTCAAGCAATTCTCCCGCCTCAGCCTCCTG ACGATCTTGGCTCACTGCAGCCTCCGCCTGTCGGGTTCAAGCAATTCTCCCGCCTCAGCCTCCTG T C AC008758.1 Ensembl:ENSG00000196826 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1408238822 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_192689 24613 RMVar_ID_24613 Human_SNP_ID_658788887 A-to-I Human chr19 - 12537522 12537522 12537522 TTTGGTCAGGCTGGTCTCGAACTCCCGACCTCAGGTGATCCGCCCCCCTCGACCTCCCAAAGTGC TTTGGTCAGGCTGGTCTCGAACTCCCGACCTCGGGTGATCCGCCCCCCTCGACCTCCCAAAGTGC T C AC008758.1,AC010422.6,ZNF564 Ensembl:ENSG00000196826,Ensembl:ENSG00000269693,Ensembl:ENSG00000249709 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs905774644 Functional Loss SNV dbSNP153 33..33 33 - - - 24614 RMVar_ID_24614 Human_SNP_ID_658788888 A-to-I Human chr19 - 12537522 12537522 12537522 TTTGGTCAGGCTGGTCTCGAACTCCCGACCTCAGGTGATCCGCCCCCCTCGACCTCCCAAAGTGC TTTGGTCAGGCTGGTCTCGAACTCCCGACCTCCGGTGATCCGCCCCCCTCGACCTCCCAAAGTGC T G AC008758.1,AC010422.6,ZNF564 Ensembl:ENSG00000196826,Ensembl:ENSG00000269693,Ensembl:ENSG00000249709 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs905774644 Functional Loss SNV dbSNP153 33..33 33 - - - 24615 RMVar_ID_24615 Human_SNP_ID_658791795 A-to-I Human chr19 - 12546609 12546609 12546609 CTCCTGCCTCAGCCTCCCGAGTAGCCTGGACTACAGGTGCCCACCACCATTCCTGGCTAATTTTT CTCCTGCCTCAGCCTCCCGAGTAGCCTGGACTGCAGGTGCCCACCACCATTCCTGGCTAATTTTT T C AC008758.1,AC010422.6,ZNF564 Ensembl:ENSG00000196826,Ensembl:ENSG00000269693,Ensembl:ENSG00000249709 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs972576476 Functional Loss SNV dbSNP153 33..33 33 - - - 24616 RMVar_ID_24616 Human_SNP_ID_658791971 A-to-I Human chr19 - 12547330 12547330 12547330 GGCTTTTCTGGTGGAAGTGGCGGCTTACATCTATAATCCCAGCACTTTGGGAGGCCGAAACAGGA GGCTTTTCTGGTGGAAGTGGCGGCTTACATCTCTAATCCCAGCACTTTGGGAGGCCGAAACAGGA T G AC008758.1,AC010422.6,ZNF564 Ensembl:ENSG00000196826,Ensembl:ENSG00000269693,Ensembl:ENSG00000249709 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404384810 Functional Loss SNV dbSNP153 33..33 33 - - - 24617 RMVar_ID_24617 Human_SNP_ID_658792288 A-to-I Human chr19 - 12548488 12548488 12548488 AAAATTGGCCGGGCACGGTGGCTCACGCCTTTAATCCCAGCACTTTGGGAGGCCAAGGTGTGCGG AAAATTGGCCGGGCACGGTGGCTCACGCCTTTCATCCCAGCACTTTGGGAGGCCAAGGTGTGCGG T G AC008758.1,AC010422.6,ZNF564 Ensembl:ENSG00000196826,Ensembl:ENSG00000269693,Ensembl:ENSG00000249709 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1339375544 Functional Loss SNV dbSNP153 33..33 33 - - - 24618 RMVar_ID_24618 Human_SNP_ID_658792929 A-to-I Human chr19 - 12550487 12550487 12550487 CACGACCGGCTACTTTTTGTATTTTTGGTAGAAACTGGGTTTCTCCATGTTGGCCAGGTTGGTCT CACGACCGGCTACTTTTTGTATTTTTGGTAGAGACTGGGTTTCTCCATGTTGGCCAGGTTGGTCT T C AC008758.1,AC010422.6,ZNF564 Ensembl:ENSG00000196826,Ensembl:ENSG00000269693,Ensembl:ENSG00000249709 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs796864689 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13544373 Human_Splice_Rec_1962097 24619 RMVar_ID_24619 Human_SNP_ID_658793978 A-to-I Human chr19 + 12554251 12554251 12554251 CCAGGAGGCAGAGGTTGCAGTGAGCCGAGATCACTACTGCACTGCAGCCTGGCCGACAGAGTGAG CCAGGAGGCAGAGGTTGCAGTGAGCCGAGATCGCTACTGCACTGCAGCCTGGCCGACAGAGTGAG A G RF00017-1304 RNACentral:URS0000990DE9 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1157909852 Functional Loss SNV dbSNP153 33..33 33 - - - 24620 RMVar_ID_24620 Human_SNP_ID_658795677 A-to-I Human chr19 + 12560209 12560209 12560209 GCCCAGAGCGACCCTTCCTGGCCATCCTGGGCAGAACTAAAGTTGCAGACAAGATCCAGCTGATC GCCCAGAGCGACCCTTCCTGGCCATCCTGGGCGGAACTAAAGTTGCAGACAAGATCCAGCTGATC A G PGK1P2 Ensembl:ENSG00000213290 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879209736 Functional Loss SNV dbSNP153 33..33 33 - - - 24621 RMVar_ID_24621 Human_SNP_ID_658799307 A-to-I Human chr19 - 12574842 12574842 12574842 AAGAAGGCTAGGCGTGGTGGTTTACACCTGTAATCACAGCTACTCAGGAGACTGAGGCAGGAGTA AAGAAGGCTAGGCGTGGTGGTTTACACCTGTAGTCACAGCTACTCAGGAGACTGAGGCAGGAGTA T C AC010422.6 Ensembl:ENSG00000269693 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1465014823 Functional Loss SNV dbSNP153 33..33 33 - - - 24622 RMVar_ID_24622 Human_SNP_ID_658807273 A-to-I Human chr19 - 12605429 12605429 12605429 TCTCCCAGGCTGGAGTGCAGTGGCAGGATCATAGCTCATTGCAGCCTTCAACTCTTGGGATCAAG TCTCCCAGGCTGGAGTGCAGTGGCAGGATCATGGCTCATTGCAGCCTTCAACTCTTGGGATCAAG T C ZNF490 Ensembl:ENSG00000188033 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1164380312 Functional Loss SNV dbSNP153 33..33 33 - - - 24623 RMVar_ID_24623 Human_SNP_ID_658810033 A-to-I Human chr19 + 12615218 12615218 12615218 TCGTATTTTCTGTAGAGATGGGGTTTCGCCATATTGCCCAGGCTGGTCTGGAACTCCTGGGCTCG TCGTATTTTCTGTAGAGATGGGGTTTCGCCATGTTGCCCAGGCTGGTCTGGAACTCCTGGGCTCG A G ZNF791 Ensembl:ENSG00000173875 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946935675 Functional Loss SNV dbSNP153 33..33 33 - - - 24624 RMVar_ID_24624 Human_SNP_ID_658814585 A-to-I Human chr19 + 12629799 12629799 12629799 AGCTACTTGGGAGGCTGAGGCAGGAGAATGGCATAAACCCAGGAGGCCGAGCTGACAGTGAGCTG AGCTACTTGGGAGGCTGAGGCAGGAGAATGGCGTAAACCCAGGAGGCCGAGCTGACAGTGAGCTG A G ZNF791 Ensembl:ENSG00000173875 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs562481011 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25383675,Human_RBP_ID_26982765 24625 RMVar_ID_24625 Human_SNP_ID_658814586 A-to-I Human chr19 + 12629801 12629801 12629801 CTACTTGGGAGGCTGAGGCAGGAGAATGGCATAAACCCAGGAGGCCGAGCTGACAGTGAGCTGAG CTACTTGGGAGGCTGAGGCAGGAGAATGGCATGAACCCAGGAGGCCGAGCTGACAGTGAGCTGAG A G ZNF791 Ensembl:ENSG00000173875 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924783935 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26982765 24626 RMVar_ID_24626 Human_SNP_ID_658814588 A-to-I Human chr19 + 12629807 12629807 12629807 GGGAGGCTGAGGCAGGAGAATGGCATAAACCCAGGAGGCCGAGCTGACAGTGAGCTGAGATCCGG GGGAGGCTGAGGCAGGAGAATGGCATAAACCCGGGAGGCCGAGCTGACAGTGAGCTGAGATCCGG A G ZNF791 Ensembl:ENSG00000173875 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1189845218 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4502021,Human_RBP_ID_6720580 24627 RMVar_ID_24627 Human_SNP_ID_658815050 A-to-I Human chr19 + 12631695 12631695 12631695 TGGAGGCTGCAGTGAGCTGAGATTGTGCCACTACACTCCAGCCTGGGCAACAGAGCAAGACTCCA TGGAGGCTGCAGTGAGCTGAGATTGTGCCACTGCACTCCAGCCTGGGCAACAGAGCAAGACTCCA A G ZNF791 Ensembl:ENSG00000173875 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1228680315 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23310098 Human_miRNA_ID_95814 24628 RMVar_ID_24628 Human_SNP_ID_658815302 A-to-I Human chr19 + 12632671 12632671 12632671 GGGCATGTTGGAGGGCACCTGTAATCTCAGCTACTTGGGAGGCTGAGGCAGGAGAAATGCTTGAA GGGCATGTTGGAGGGCACCTGTAATCTCAGCTGCTTGGGAGGCTGAGGCAGGAGAAATGCTTGAA A G ZNF791 Ensembl:ENSG00000173875 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1264695029 Functional Loss SNV dbSNP153 33..33 33 - - - 24629 RMVar_ID_24629 Human_SNP_ID_658815311 A-to-I Human chr19 + 12632714 12632713 12632715 TGAGGCAGGAGAAATGCTTGAACCTGGAAGTCAGAGGTTGCAGTGAGCCAAGATCACACCACTGC TGAGGCAGGAGAAATGCTTGAACCTGGAAGTC__AGGTTGCAGTGAGCCAAGATCACACCACTGC CAG C ZNF791 Ensembl:ENSG00000173875 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1271114950 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_2556262 24630 RMVar_ID_24630 Human_SNP_ID_658815312 A-to-I Human chr19 + 12632714 12632714 12632714 TGAGGCAGGAGAAATGCTTGAACCTGGAAGTCAGAGGTTGCAGTGAGCCAAGATCACACCACTGC TGAGGCAGGAGAAATGCTTGAACCTGGAAGTCGGAGGTTGCAGTGAGCCAAGATCACACCACTGC A G ZNF791 Ensembl:ENSG00000173875 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1236381311 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2556262 24631 RMVar_ID_24631 Human_SNP_ID_658818815 A-to-I Human chr19 - 12645631 12645631 12645631 AAAAAAAAAGTAGGCAGTGCGTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGTC AAAAAAAAAGTAGGCAGTGCGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGTC T C AC010422.3 Ensembl:ENSG00000269242 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1169485645 Functional Loss SNV dbSNP153 33..33 33 - - - 24632 RMVar_ID_24632 Human_SNP_ID_658823433 A-to-I Human chr19 - 12659430 12659430 12659430 GGGCGTGATGGCACTCATCTGTAAGACCAGCTACTCGGCAGGCTGAGGCAGGAGAATCGCTGGAA GGGCGTGATGGCACTCATCTGTAAGACCAGCTGCTCGGCAGGCTGAGGCAGGAGAATCGCTGGAA T C MAN2B1 Ensembl:ENSG00000104774 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs555285695 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109163,RMVar_hsa_circ_192702,RMVar_hsa_circ_95806,RMVar_hsa_circ_106184,RMVar_hsa_circ_192703,RMVar_hsa_circ_192704,RMVar_hsa_circ_33174,RMVar_hsa_circ_376707 24633 RMVar_ID_24633 Human_SNP_ID_658823493 A-to-I Human chr19 - 12659707 12659707 12659707 TCTAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCATGTGCCACCAACCCTG TCTAGTGATTCTCCTGCCTCAGCCTCCCAAGTGGCTGGGACTACAGGCATGTGCCACCAACCCTG T C MAN2B1 Ensembl:ENSG00000104774 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs889361013 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109163,RMVar_hsa_circ_192702,RMVar_hsa_circ_95806,RMVar_hsa_circ_106184,RMVar_hsa_circ_192703,RMVar_hsa_circ_192704,RMVar_hsa_circ_33174,RMVar_hsa_circ_376707 24634 RMVar_ID_24634 Human_SNP_ID_658823630 A-to-I Human chr19 - 12660336 12660336 12660336 CACCACGCCCAGCTAATTTTTGTATTTTTAGTAGACAGGGTTTCACCATGTTGGCCAGGATGGTC CACCACGCCCAGCTAATTTTTGTATTTTTAGTGGACAGGGTTTCACCATGTTGGCCAGGATGGTC T C MAN2B1 Ensembl:ENSG00000104774 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1257878557 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109163,RMVar_hsa_circ_192702,RMVar_hsa_circ_95806,RMVar_hsa_circ_106184,RMVar_hsa_circ_192703,RMVar_hsa_circ_192704,RMVar_hsa_circ_33174,RMVar_hsa_circ_376707 24635 RMVar_ID_24635 Human_SNP_ID_658824083 A-to-I Human chr19 - 12661907 12661907 12661907 CTGGCAGGTGGAGGTTGCAGTGAGCCGAGATCACGTCACTTCACTCTAGCTTGGGCAGCAGAGTG CTGGCAGGTGGAGGTTGCAGTGAGCCGAGATCCCGTCACTTCACTCTAGCTTGGGCAGCAGAGTG T G MAN2B1 Ensembl:ENSG00000104774 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1568306201 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109163,RMVar_hsa_circ_95806,RMVar_hsa_circ_192703,RMVar_hsa_circ_192704,RMVar_hsa_circ_303855 24636 RMVar_ID_24636 Human_SNP_ID_658827200 A-to-I Human chr19 - 12671148 12671148 12671148 AATTTTTGCATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGATCTCAACCTCCTGA AATTTTTGCATTTTTAGTAGAGACGGGGTTTCTCCATGTTGGCCAGGCTGATCTCAACCTCCTGA T A AC010422.8 Ensembl:ENSG00000285589 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs915334012 Functional Loss SNV dbSNP153 33..33 33 - - - 24637 RMVar_ID_24637 Human_SNP_ID_658827247 A-to-I Human chr19 - 12671314 12671314 12671314 ATTTTATCTTTTTTTTTTTGAGATGGAGTCTCACTTTGTCGCCCAGGCTGGAGTGCAGTGGCACA ATTTTATCTTTTTTTTTTTGAGATGGAGTCTCGCTTTGTCGCCCAGGCTGGAGTGCAGTGGCACA T C AC010422.8 Ensembl:ENSG00000285589 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1410146143 Functional Loss SNV dbSNP153 33..33 33 - - - 24638 RMVar_ID_24638 Human_SNP_ID_658827432 A-to-I Human chr19 - 12671924 12671923 12671925 TGGGAGGCCAGGGCAGGTGGATCACGAGGTCAAGAGATGGAGACCCTCCTGGCCAACATGGCGAA TGGGAGGCCAGGGCAGGTGGATCACGAGGTC__GAGATGGAGACCCTCCTGGCCAACATGGCGAA CTT C AC010422.8 Ensembl:ENSG00000285589 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1287963408 Functional Loss DEL dbSNP153 32..33 33 - - - 24639 RMVar_ID_24639 Human_SNP_ID_658828089 A-to-I Human chr19 + 12673684 12673684 12673684 ATGATCCACCCACCTCAGCCTTCCCAAGTGCTAGGATTACAGGCGTAAGCCACCACACCCGGCCC ATGATCCACCCACCTCAGCCTTCCCAAGTGCTGGGATTACAGGCGTAAGCCACCACACCCGGCCC A G WDR83 Ensembl:ENSG00000123154 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs911909897 Functional Loss SNV dbSNP153 33..33 33 - - - 24640 RMVar_ID_24640 Human_SNP_ID_658828146 A-to-I Human chr19 - 12673879 12673879 12673879 CCTGGCCAACATGGTGAAACCCTGTCTCTACTAAAAATACAAAAATTAGCCAGGTATGGTGGTAG CCTGGCCAACATGGTGAAACCCTGTCTCTACTGAAAATACAAAAATTAGCCAGGTATGGTGGTAG T C AC010422.8 Ensembl:ENSG00000285589 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1568315380 Functional Loss SNV dbSNP153 33..33 33 - - - 24641 RMVar_ID_24641 Human_SNP_ID_658829384 A-to-I Human chr19 - 12677366 12677366 12677366 AGAACCACATCCCTGTGTTTAGTCCCGCACTTACAGACGGCTCGCTGGGCGACATGATCTTCTTC AGAACCACATCCCTGTGTTTAGTCCCGCACTTGCAGACGGCTCGCTGGGCGACATGATCTTCTTC T C DHPS,AC010422.8 Ensembl:ENSG00000095059,Ensembl:ENSG00000285589 Protein coding,Protein coding CDS,3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs764549648 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_513316,Human_RBP_ID_4502318,Human_RBP_ID_18722526 Human_Splice_Rec_1962566,Human_Splice_Rec_1962567,Human_Splice_Rec_1962602,Human_Splice_Rec_1962603,Human_Splice_Rec_1962618,Human_Splice_Rec_1962619,Human_Splice_Rec_1962628,Human_Splice_Rec_1962629,Human_Splice_Rec_1962642,Human_Splice_Rec_1962643,Human_Splice_Rec_1962654,Human_Splice_Rec_1962655,Human_Splice_Rec_1962670,Human_Splice_Rec_1962671,Human_Splice_Rec_1962688,Human_Splice_Rec_1962689,Human_Splice_Rec_1962702,Human_Splice_Rec_1962703,Human_Splice_Rec_1962714,Human_Splice_Rec_1962715,Human_Splice_Rec_1962722,Human_Splice_Rec_1962726,Human_Splice_Rec_1962727,Human_Splice_Rec_1962738,Human_Splice_Rec_1962739,Human_Splice_Rec_1962748,Human_Splice_Rec_1962758,Human_Splice_Rec_1962768,Human_Splice_Rec_1962778 RMVar_hsa_circ_91152,RMVar_hsa_circ_10919,RMVar_hsa_circ_126140,RMVar_hsa_circ_332088,RMVar_hsa_circ_192720,RMVar_hsa_circ_329021,RMVar_hsa_circ_192722,RMVar_hsa_circ_192723,RMVar_hsa_circ_279453 24642 RMVar_ID_24642 Human_SNP_ID_658829526 A-to-I Human chr19 - 12677747 12677747 12677747 CCTGTAATCCTAGCTACTCGGGAGGCTGAAGCAGGAGAATCACTGGAACCCAGGAGGCAGAGGTT CCTGTAATCCTAGCTACTCGGGAGGCTGAAGCGGGAGAATCACTGGAACCCAGGAGGCAGAGGTT T C DHPS,AC010422.8 Ensembl:ENSG00000095059,Ensembl:ENSG00000285589 Protein coding,Protein coding intron,intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1425761121 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91152,RMVar_hsa_circ_10919,RMVar_hsa_circ_126140,RMVar_hsa_circ_192720,RMVar_hsa_circ_329021,RMVar_hsa_circ_192722,RMVar_hsa_circ_192723,RMVar_hsa_circ_279453 24643 RMVar_ID_24643 Human_SNP_ID_658829746 A-to-I Human chr19 - 12678461 12678459 12678461 CCAGCCTACTTACTCTTTCTTTTTTACGAGACAGGGTCTCATTCTGTTTCCCAGGCTGGAGTGCA CCAGCCTACTTACTCTTTCTTTTTTACGAGAC__GGTCTCATTCTGTTTCCCAGGCTGGAGTGCA CCT C DHPS,AC010422.8 Ensembl:ENSG00000095059,Ensembl:ENSG00000285589 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474378009 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_91152,RMVar_hsa_circ_10919,RMVar_hsa_circ_126140,RMVar_hsa_circ_192720,RMVar_hsa_circ_329021,RMVar_hsa_circ_192722,RMVar_hsa_circ_192723,RMVar_hsa_circ_279453 24644 RMVar_ID_24644 Human_SNP_ID_658829792 A-to-I Human chr19 - 12678686 12678678 12678687 CAGCTCACTGCACCCTCCACCTCCCAGGTTCAAGTGATTCTCCCGCCTCACCCTCCTGAGTAGCT CAGCTCACTGCACCCTCCACCTCCCAGGTTC_________TCCCGCCTCACCCTCCTGAGTAGCT AGAATCACTT A DHPS,AC010422.8 Ensembl:ENSG00000095059,Ensembl:ENSG00000285589 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs945294279 Functional Loss DEL dbSNP153 32..40 33 - - - RMVar_hsa_circ_91152,RMVar_hsa_circ_10919,RMVar_hsa_circ_126140,RMVar_hsa_circ_192720,RMVar_hsa_circ_329021,RMVar_hsa_circ_192722,RMVar_hsa_circ_192723,RMVar_hsa_circ_279453 24645 RMVar_ID_24645 Human_SNP_ID_658832908 A-to-I Human chr19 - 12686627 12686627 12686627 GTTTTTAACTTTTTGTAGAGATGGTTCTTACTATGTTGCCCAGGCTGGTCTTGAACTCCTGGCCT GTTTTTAACTTTTTGTAGAGATGGTTCTTACTGTGTTGCCCAGGCTGGTCTTGAACTCCTGGCCT T C AC010422.2 Ensembl:ENSG00000268945 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs891706507 Functional Loss SNV dbSNP153 33..33 33 - - - 24646 RMVar_ID_24646 Human_SNP_ID_658833125 A-to-I Human chr19 - 12687379 12687379 12687379 TCACCCATGTTGGAGTGCAGTGGTGCGATCTCAGCTCACTTTCAACCTCCACCTCCCGGGCTCAA TCACCCATGTTGGAGTGCAGTGGTGCGATCTCGGCTCACTTTCAACCTCCACCTCCCGGGCTCAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1300446697 Functional Loss SNV dbSNP153 33..33 33 - - - 24647 RMVar_ID_24647 Human_SNP_ID_658838598 A-to-I Human chr19 - 12704204 12704204 12704204 CCACTATGCCTGGCTAATTTTATTGTATTTTTAGTAAAGACAGGGTTTTGCCATGTTGGCCAGGC CCACTATGCCTGGCTAATTTTATTGTATTTTTGGTAAAGACAGGGTTTTGCCATGTTGGCCAGGC T C TNPO2 Ensembl:ENSG00000105576 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1193689899 Functional Loss SNV dbSNP153 33..33 33 - - - 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_192743 24648 RMVar_ID_24648 Human_SNP_ID_658838601 A-to-I Human chr19 - 12704210 12704210 12704210 CGTGTCCCACTATGCCTGGCTAATTTTATTGTATTTTTAGTAAAGACAGGGTTTTGCCATGTTGG CGTGTCCCACTATGCCTGGCTAATTTTATTGTGTTTTTAGTAAAGACAGGGTTTTGCCATGTTGG T C TNPO2 Ensembl:ENSG00000105576 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1032436350 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25383978 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_192743 24649 RMVar_ID_24649 Human_SNP_ID_658838767 A-to-I Human chr19 - 12704811 12704811 12704811 AGGCATGGTGGTAGGCGCCTGTAATCCCAGCTACTTGGAAGGCTGAGGCAGGAGAATTGCTTGAA AGGCATGGTGGTAGGCGCCTGTAATCCCAGCTGCTTGGAAGGCTGAGGCAGGAGAATTGCTTGAA T C TNPO2 Ensembl:ENSG00000105576 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs935814377 Functional Loss SNV dbSNP153 33..33 33 - - - 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_192743 24650 RMVar_ID_24650 Human_SNP_ID_658838768 A-to-I Human chr19 - 12704811 12704811 12704811 AGGCATGGTGGTAGGCGCCTGTAATCCCAGCTACTTGGAAGGCTGAGGCAGGAGAATTGCTTGAA AGGCATGGTGGTAGGCGCCTGTAATCCCAGCTCCTTGGAAGGCTGAGGCAGGAGAATTGCTTGAA T G TNPO2 Ensembl:ENSG00000105576 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs935814377 Functional Loss SNV dbSNP153 33..33 33 - - - 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_192743 24651 RMVar_ID_24651 Human_SNP_ID_658838771 A-to-I Human chr19 - 12704820 12704820 12704820 AAATTAGCCAGGCATGGTGGTAGGCGCCTGTAATCCCAGCTACTTGGAAGGCTGAGGCAGGAGAA AAATTAGCCAGGCATGGTGGTAGGCGCCTGTAGTCCCAGCTACTTGGAAGGCTGAGGCAGGAGAA T C TNPO2 Ensembl:ENSG00000105576 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1464865543 Functional Loss SNV dbSNP153 33..33 33 - - - 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_192743 24652 RMVar_ID_24652 Human_SNP_ID_658838799 A-to-I Human chr19 - 12704957 12704957 12704957 AATAGAAAATGTGAGGCCAGGTGCTCACGCCTATAATCCAGCACTTTGGGAGGCTGTGGCAGGTG AATAGAAAATGTGAGGCCAGGTGCTCACGCCTGTAATCCAGCACTTTGGGAGGCTGTGGCAGGTG T C TNPO2 Ensembl:ENSG00000105576 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs573374076 Functional Loss SNV dbSNP153 33..33 33 - - - 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_192743 24653 RMVar_ID_24653 Human_SNP_ID_658839764 A-to-I Human chr19 - 12707959 12707959 12707959 AAAATTAGCCACACGTGGTGGCCCACGCCTGTAGTCCCAGCTACTGGGGAGGTTGAGGCAGGAAA AAAATTAGCCACACGTGGTGGCCCACGCCTGTGGTCCCAGCTACTGGGGAGGTTGAGGCAGGAAA T C TNPO2 Ensembl:ENSG00000105576 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1229373374 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105206,RMVar_hsa_circ_89937,RMVar_hsa_circ_126336,RMVar_hsa_circ_27703,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_42944,RMVar_hsa_circ_192744,RMVar_hsa_circ_118183,RMVar_hsa_circ_192741,RMVar_hsa_circ_192742,RMVar_hsa_circ_100778,RMVar_hsa_circ_192743,RMVar_hsa_circ_373724,RMVar_hsa_circ_341201,RMVar_hsa_circ_98766,RMVar_hsa_circ_44442,RMVar_hsa_circ_106191,RMVar_hsa_circ_192748,RMVar_hsa_circ_192749,RMVar_hsa_circ_87391,RMVar_hsa_circ_84552,RMVar_hsa_circ_192750,RMVar_hsa_circ_192751,RMVar_hsa_circ_192754,RMVar_hsa_circ_123805,RMVar_hsa_circ_192756 24654 RMVar_ID_24654 Human_SNP_ID_658839987 A-to-I Human chr19 - 12708824 12708824 12708824 TCTTACTGTCCAGGCTGGAGTGCAATGGCGCAATCTTGACTCACTGCAACCTCTGCCTCCCGAGT TCTTACTGTCCAGGCTGGAGTGCAATGGCGCAGTCTTGACTCACTGCAACCTCTGCCTCCCGAGT T C TNPO2 Ensembl:ENSG00000105576 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs956650366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13371095,Human_RBP_ID_23174054 RMVar_hsa_circ_105206,RMVar_hsa_circ_89937,RMVar_hsa_circ_126336,RMVar_hsa_circ_27703,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_42944,RMVar_hsa_circ_192744,RMVar_hsa_circ_118183,RMVar_hsa_circ_192741,RMVar_hsa_circ_192742,RMVar_hsa_circ_100778,RMVar_hsa_circ_192743,RMVar_hsa_circ_373724,RMVar_hsa_circ_341201,RMVar_hsa_circ_98766,RMVar_hsa_circ_44442,RMVar_hsa_circ_106191,RMVar_hsa_circ_192748,RMVar_hsa_circ_192749,RMVar_hsa_circ_87391,RMVar_hsa_circ_84552,RMVar_hsa_circ_192750,RMVar_hsa_circ_192751,RMVar_hsa_circ_192754,RMVar_hsa_circ_123805,RMVar_hsa_circ_192756 24655 RMVar_ID_24655 Human_SNP_ID_658840026 A-to-I Human chr19 - 12708949 12708949 12708949 CTGCAACAACATTCTGCCTCCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCAGAGTAGCTTGG CTGCAACAACATTCTGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCAGAGTAGCTTGG T C TNPO2 Ensembl:ENSG00000105576 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1325325381 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105206,RMVar_hsa_circ_89937,RMVar_hsa_circ_126336,RMVar_hsa_circ_27703,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_42944,RMVar_hsa_circ_192744,RMVar_hsa_circ_118183,RMVar_hsa_circ_192741,RMVar_hsa_circ_192742,RMVar_hsa_circ_100778,RMVar_hsa_circ_192743,RMVar_hsa_circ_373724,RMVar_hsa_circ_341201,RMVar_hsa_circ_98766,RMVar_hsa_circ_44442,RMVar_hsa_circ_106191,RMVar_hsa_circ_192748,RMVar_hsa_circ_192749,RMVar_hsa_circ_87391,RMVar_hsa_circ_84552,RMVar_hsa_circ_192750,RMVar_hsa_circ_192751,RMVar_hsa_circ_192754,RMVar_hsa_circ_123805,RMVar_hsa_circ_192756 24656 RMVar_ID_24656 Human_SNP_ID_658841248 A-to-I Human chr19 - 12713039 12713039 12713039 TGGGTCAAGAGCTTTCCTGCAGGCTGAGTGCCATGGCTCACGCCTATAATCCTAGCACTTTGGGA TGGGTCAAGAGCTTTCCTGCAGGCTGAGTGCCGTGGCTCACGCCTATAATCCTAGCACTTTGGGA T C TNPO2 Ensembl:ENSG00000105576 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs774839712 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105206,RMVar_hsa_circ_89937,RMVar_hsa_circ_27703,RMVar_hsa_circ_192730,RMVar_hsa_circ_120313,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_81765,RMVar_hsa_circ_42944,RMVar_hsa_circ_192744,RMVar_hsa_circ_118183,RMVar_hsa_circ_192741,RMVar_hsa_circ_192742,RMVar_hsa_circ_100778,RMVar_hsa_circ_192743,RMVar_hsa_circ_341201,RMVar_hsa_circ_98766,RMVar_hsa_circ_192749,RMVar_hsa_circ_87391,RMVar_hsa_circ_192750,RMVar_hsa_circ_192754,RMVar_hsa_circ_123805,RMVar_hsa_circ_112276,RMVar_hsa_circ_118305,RMVar_hsa_circ_192759,RMVar_hsa_circ_192760,RMVar_hsa_circ_124916,RMVar_hsa_circ_109249,RMVar_hsa_circ_192761,RMVar_hsa_circ_192762,RMVar_hsa_circ_192763 24657 RMVar_ID_24657 Human_SNP_ID_658843025 A-to-I Human chr19 - 12719716 12719715 12719716 CGGCTCACTGCAACCTTCACCTGCTGGGTTCAAGCGATTCCCCTGCGTCAGCCTCCCAAGTAGTT CGGCTCACTGCAACCTTCACCTGCTGGGTTCA_GCGATTCCCCTGCGTCAGCCTCCCAAGTAGTT CT C TNPO2 Ensembl:ENSG00000105576 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1175918859 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_8477321,Human_RBP_ID_13371336 RMVar_hsa_circ_27703,RMVar_hsa_circ_99856,RMVar_hsa_circ_192738,RMVar_hsa_circ_111022,RMVar_hsa_circ_81765,RMVar_hsa_circ_192744,RMVar_hsa_circ_118183,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 24658 RMVar_ID_24658 Human_SNP_ID_658843026 A-to-I Human chr19 - 12719716 12719716 12719716 CGGCTCACTGCAACCTTCACCTGCTGGGTTCAAGCGATTCCCCTGCGTCAGCCTCCCAAGTAGTT CGGCTCACTGCAACCTTCACCTGCTGGGTTCAGGCGATTCCCCTGCGTCAGCCTCCCAAGTAGTT T C TNPO2 Ensembl:ENSG00000105576 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs186176243 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8477321,Human_RBP_ID_13371336 RMVar_hsa_circ_27703,RMVar_hsa_circ_99856,RMVar_hsa_circ_192738,RMVar_hsa_circ_111022,RMVar_hsa_circ_81765,RMVar_hsa_circ_192744,RMVar_hsa_circ_118183,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 24659 RMVar_ID_24659 Human_SNP_ID_658843038 A-to-I Human chr19 - 12719752 12719752 12719752 CTCTGTCGCCCAGACTGGAATGCAGAGGCGCAATCTCGGCTCACTGCAACCTTCACCTGCTGGGT CTCTGTCGCCCAGACTGGAATGCAGAGGCGCAGTCTCGGCTCACTGCAACCTTCACCTGCTGGGT T C TNPO2 Ensembl:ENSG00000105576 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs886333705 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25384156 RMVar_hsa_circ_27703,RMVar_hsa_circ_99856,RMVar_hsa_circ_192738,RMVar_hsa_circ_111022,RMVar_hsa_circ_81765,RMVar_hsa_circ_192744,RMVar_hsa_circ_118183,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 24660 RMVar_ID_24660 Human_SNP_ID_658843043 A-to-I Human chr19 - 12719761 12719761 12719761 GGAGTCTTGCTCTGTCGCCCAGACTGGAATGCAGAGGCGCAATCTCGGCTCACTGCAACCTTCAC GGAGTCTTGCTCTGTCGCCCAGACTGGAATGCGGAGGCGCAATCTCGGCTCACTGCAACCTTCAC T C TNPO2 Ensembl:ENSG00000105576 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1056194271 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27703,RMVar_hsa_circ_99856,RMVar_hsa_circ_192738,RMVar_hsa_circ_111022,RMVar_hsa_circ_81765,RMVar_hsa_circ_192744,RMVar_hsa_circ_118183,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 24661 RMVar_ID_24661 Human_SNP_ID_658846743 A-to-I Human chr19 - 12732085 12732085 12732085 AGTCTACTTCTTGTTGCCCAGGCTGGAGTGCAATGGTGCAACCTCGGCTCACTGCAACCTCCTCC AGTCTACTTCTTGTTGCCCAGGCTGGAGTGCAGTGGTGCAACCTCGGCTCACTGCAACCTCCTCC T C TRIR Ensembl:ENSG00000123144 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1034133446 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111334,RMVar_hsa_circ_192775,RMVar_hsa_circ_192778 24662 RMVar_ID_24662 Human_SNP_ID_658846906 A-to-I Human chr19 - 12732652 12732652 12732652 CTGGGAGGTGGAGGTTGCAGTGAGCTGAGATCATGCCACTGCACTCCAGCCTCGACAGTAAGACT CTGGGAGGTGGAGGTTGCAGTGAGCTGAGATCGTGCCACTGCACTCCAGCCTCGACAGTAAGACT T C TRIR Ensembl:ENSG00000123144 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1419997825 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9930038,Human_RBP_ID_13371523 RMVar_hsa_circ_111334,RMVar_hsa_circ_192775,RMVar_hsa_circ_192778 24663 RMVar_ID_24663 Human_SNP_ID_658846998 A-to-I Human chr19 - 12732972 12732964 12732973 TTGAGCCCAGGAGATTCAGGCTGCAGTGAGCCATGATTGCACCACTGCGCTCTAGCCTGGATGAC TTGAGCCCAGGAGATTCAGGCTGCAGTGAGC_________ACCACTGCGCTCTAGCCTGGATGAC TGCAATCATG T TRIR Ensembl:ENSG00000123144 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041874915 Functional Loss DEL dbSNP153 32..40 33 - - - Human_RBP_ID_13371528 RMVar_hsa_circ_111334,RMVar_hsa_circ_192775,RMVar_hsa_circ_192778 24664 RMVar_ID_24664 Human_SNP_ID_658847001 A-to-I Human chr19 - 12732972 12732972 12732972 TTGAGCCCAGGAGATTCAGGCTGCAGTGAGCCATGATTGCACCACTGCGCTCTAGCCTGGATGAC TTGAGCCCAGGAGATTCAGGCTGCAGTGAGCCGTGATTGCACCACTGCGCTCTAGCCTGGATGAC T C TRIR Ensembl:ENSG00000123144 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1482016401 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13371528 RMVar_hsa_circ_111334,RMVar_hsa_circ_192775,RMVar_hsa_circ_192778 24665 RMVar_ID_24665 Human_SNP_ID_658864648 A-to-I Human chr19 + 12791895 12791895 12791895 ACTACAAACTCCTGAAACCGAGCCTGGCGGTCAACCTGGCCGACCCCTACCGGAGTCTCAAAGCG ACTACAAACTCCTGAAACCGAGCCTGGCGGTCGACCTGGCCGACCCCTACCGGAGTCTCAAAGCG A G JUNB Ensembl:ENSG00000171223 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs767015453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27463559 24666 RMVar_ID_24666 Human_SNP_ID_658870586 A-to-I Human chr19 + 12811069 12811069 12811069 GTGATCCTCCTGCCTTGGACTCCCAAATAGCTAGGATTACAGGTGTGAACTACTGTGCCTGGCTG GTGATCCTCCTGCCTTGGACTCCCAAATAGCTGGGATTACAGGTGTGAACTACTGTGCCTGGCTG A G THSD8,RNASEH2A Ensembl:ENSG00000284491,Ensembl:ENSG00000104889 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1324432590 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108452,RMVar_hsa_circ_77476,RMVar_hsa_circ_192795,RMVar_hsa_circ_192796 24667 RMVar_ID_24667 Human_SNP_ID_658871919 A-to-I Human chr19 + 12815658 12815658 12815658 ACAGTCTTAAGTCACTGCAACCCCCACTTCCCAGGTTCAAGCAATTCTCCCACCTCAGCCTCCCG ACAGTCTTAAGTCACTGCAACCCCCACTTCCCGGGTTCAAGCAATTCTCCCACCTCAGCCTCCCG A G RF00017-1304 RNACentral:URS0000990DE9 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1568389575 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17915304 24668 RMVar_ID_24668 Human_SNP_ID_658883752 A-to-I Human chr19 + 12859263 12859262 12859264 CACCATTCATGGGTAATTTTTCTATTTTTAGCAGAGACAGGATTTCGCCATGTTTGCCAGGCTAG CACCATTCATGGGTAATTTTTCTATTTTTAGC__AGACAGGATTTCGCCATGTTTGCCAGGCTAG CAG C MAST1 Ensembl:ENSG00000105613 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1419861568 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_99212,RMVar_hsa_circ_117694,RMVar_hsa_circ_192806,RMVar_hsa_circ_192807,RMVar_hsa_circ_12715 24669 RMVar_ID_24669 Human_SNP_ID_658883754 A-to-I Human chr19 + 12859269 12859269 12859269 TCATGGGTAATTTTTCTATTTTTAGCAGAGACAGGATTTCGCCATGTTTGCCAGGCTAGTCTTGA TCATGGGTAATTTTTCTATTTTTAGCAGAGACGGGATTTCGCCATGTTTGCCAGGCTAGTCTTGA A G MAST1 Ensembl:ENSG00000105613 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs539721351 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99212,RMVar_hsa_circ_117694,RMVar_hsa_circ_192806,RMVar_hsa_circ_192807,RMVar_hsa_circ_12715 24670 RMVar_ID_24670 Human_SNP_ID_658894209 A-to-I Human chr19 - 12894105 12894105 12894105 TTCATCTTGAAGCAGCTGAACACCTCCGAGACACCACGGAAGAGGGCCAACGTCCACTTAGCGCA TTCATCTTGAAGCAGCTGAACACCTCCGAGACGCCACGGAAGAGGGCCAACGTCCACTTAGCGCA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs918232468 Functional Loss SNV dbSNP153 33..33 33 - - - 24671 RMVar_ID_24671 Human_SNP_ID_658894210 A-to-I Human chr19 - 12894107 12894107 12894107 GCTTCATCTTGAAGCAGCTGAACACCTCCGAGACACCACGGAAGAGGGCCAACGTCCACTTAGCG GCTTCATCTTGAAGCAGCTGAACACCTCCGAGGCACCACGGAAGAGGGCCAACGTCCACTTAGCG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1290036718 Functional Loss SNV dbSNP153 33..33 33 - - - 24672 RMVar_ID_24672 Human_SNP_ID_658894214 A-to-I Human chr19 - 12894116 12894116 12894116 AGATGTTCAGCTTCATCTTGAAGCAGCTGAACACCTCCGAGACACCACGGAAGAGGGCCAACGTC AGATGTTCAGCTTCATCTTGAAGCAGCTGAACGCCTCCGAGACACCACGGAAGAGGGCCAACGTC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879191946 Functional Loss SNV dbSNP153 33..33 33 - - - 24673 RMVar_ID_24673 Human_SNP_ID_658894233 A-to-I Human chr19 - 12894205 12894205 12894205 TTCTGTGGCCATACGCTTCTCATAAAAAGTACAAAGTTTGCGTTCATCGTCCACTTCAATGAGTT TTCTGTGGCCATACGCTTCTCATAAAAAGTACGAAGTTTGCGTTCATCGTCCACTTCAATGAGTT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879115966 Functional Loss SNV dbSNP153 33..33 33 - - - 24674 RMVar_ID_24674 Human_SNP_ID_658894236 A-to-I Human chr19 - 12894213 12894213 12894213 ACAGCAACTTCTGTGGCCATACGCTTCTCATAAAAAGTACAAAGTTTGCGTTCATCGTCCACTTC ACAGCAACTTCTGTGGCCATACGCTTCTCATAGAAAGTACAAAGTTTGCGTTCATCGTCCACTTC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879021899 Functional Loss SNV dbSNP153 33..33 33 - - - 24675 RMVar_ID_24675 Human_SNP_ID_658894244 A-to-I Human chr19 - 12894245 12894245 12894245 CGTAACCCTTCCATTCTTCACCCAGAGCGTCAACAGCAACTTCTGTGGCCATACGCTTCTCATAA CGTAACCCTTCCATTCTTCACCCAGAGCGTCAGCAGCAACTTCTGTGGCCATACGCTTCTCATAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878946393 Functional Loss SNV dbSNP153 33..33 33 - - - 24676 RMVar_ID_24676 Human_SNP_ID_658896397 A-to-I Human chr19 + 12900930 12900929 12900930 GGACGGGTGTGGTGGCTCACGCCTGTAATCCTAACACTTTGGGAGGCCGAGGCGGGCGGATCACG GGACGGGTGTGGTGGCTCACGCCTGTAATCCT_ACACTTTGGGAGGCCGAGGCGGGCGGATCACG TA T GCDH Ensembl:ENSG00000105607 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1203540841 Functional Loss DEL dbSNP153 33..33 33 - - - 24677 RMVar_ID_24677 Human_SNP_ID_658896837 A-to-I Human chr19 + 12902691 12902691 12902691 AACAAGTGAGCCGGGCATGATGTTGCATGCCTATAGTCTCAAGCTACTCGAGAGGCTGAGGTGAG AACAAGTGAGCCGGGCATGATGTTGCATGCCTGTAGTCTCAAGCTACTCGAGAGGCTGAGGTGAG A G GCDH Ensembl:ENSG00000105607 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs192579524 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17568469 24678 RMVar_ID_24678 Human_SNP_ID_658897428 A-to-I Human chr19 + 12904783 12904783 12904783 CAGCACTTTGTAGGCCGAGGTGGGCGGATCACAAGGTCAGGAGTTCGAGACCAGCCTGGCAACAT CAGCACTTTGTAGGCCGAGGTGGGCGGATCACTAGGTCAGGAGTTCGAGACCAGCCTGGCAACAT A T GCDH Ensembl:ENSG00000105607 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1304224604 Functional Loss SNV dbSNP153 33..33 33 - - - 24679 RMVar_ID_24679 Human_SNP_ID_658897711 A-to-I Human chr19 + 12905779 12905779 12905779 CCCACCTCAGCCTCCTGAATAGGTGGGACTACAAGCATGTGCTACCATGCACAGCTAATTTTTAA CCCACCTCAGCCTCCTGAATAGGTGGGACTACCAGCATGTGCTACCATGCACAGCTAATTTTTAA A C GCDH Ensembl:ENSG00000105607 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1191356999 Functional Loss SNV dbSNP153 33..33 33 - - - 24680 RMVar_ID_24680 Human_SNP_ID_658903782 A-to-I Human chr19 - 12926696 12926696 12926696 AAAATTAGCTGGGCATAGTAGTGCACGCCTGTAGTTGCAGCTACTCGGGAGGCTGAGGTGAAGGA AAAATTAGCTGGGCATAGTAGTGCACGCCTGTCGTTGCAGCTACTCGGGAGGCTGAGGTGAAGGA T G FARSA Ensembl:ENSG00000179115 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1158061136 Functional Loss SNV dbSNP153 33..33 33 - - - 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 24681 RMVar_ID_24681 Human_SNP_ID_658908353 A-to-I Human chr19 + 12941177 12941177 12941177 GGTAACCCAGTTAGTTAGCTGGGGCTGGGCACAGTGGCTCACCCTTACAATCACGGTACTTTGGG GGTAACCCAGTTAGTTAGCTGGGGCTGGGCACGGTGGCTCACCCTTACAATCACGGTACTTTGGG A G CALR Ensembl:ENSG00000179218 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs73505373 Functional Loss SNV dbSNP153 33..33 33 - - - 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_192844,RMVar_hsa_circ_192845,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_192850 24682 RMVar_ID_24682 Human_SNP_ID_658908403 A-to-I Human chr19 + 12941365 12941364 12941365 TTGCTGAGGCTGGAGTGCAATGGCACGATCTCAGCTCACTGCGCCCTCCGTCTCCTGGTTTCAAG TTGCTGAGGCTGGAGTGCAATGGCACGATCTC_GCTCACTGCGCCCTCCGTCTCCTGGTTTCAAG CA C CALR Ensembl:ENSG00000179218 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1168106883 Functional Loss DEL dbSNP153 33..33 33 - - - 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_192844,RMVar_hsa_circ_192845,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_192850 24683 RMVar_ID_24683 Human_SNP_ID_658908518 A-to-I Human chr19 + 12941719 12941719 12941719 GTTAGCCAGGATGGTCTCCATCTCCTGACCTCATGAACCACCCACCTTGGCCTCCCAAAGTGCTG GTTAGCCAGGATGGTCTCCATCTCCTGACCTCCTGAACCACCCACCTTGGCCTCCCAAAGTGCTG A C CALR Ensembl:ENSG00000179218 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs911581236 Functional Loss SNV dbSNP153 33..33 33 - - - 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_192844,RMVar_hsa_circ_192845,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_192850 24684 RMVar_ID_24684 Human_SNP_ID_658908519 A-to-I Human chr19 + 12941719 12941719 12941719 GTTAGCCAGGATGGTCTCCATCTCCTGACCTCATGAACCACCCACCTTGGCCTCCCAAAGTGCTG GTTAGCCAGGATGGTCTCCATCTCCTGACCTCGTGAACCACCCACCTTGGCCTCCCAAAGTGCTG A G CALR Ensembl:ENSG00000179218 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs911581236 Functional Loss SNV dbSNP153 33..33 33 - - - 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_192844,RMVar_hsa_circ_192845,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_192850 24685 RMVar_ID_24685 Human_SNP_ID_658908623 A-to-I Human chr19 + 12942098 12942098 12942098 AAGTTGGGACTTGGCCGGACACAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGC AAGTTGGGACTTGGCCGGACACAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGC A G CALR Ensembl:ENSG00000179218 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs907718603 Functional Loss SNV dbSNP153 33..33 33 - - - 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_192844,RMVar_hsa_circ_192845,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_192850 24686 RMVar_ID_24686 Human_SNP_ID_658908634 A-to-I Human chr19 + 12942142 12942142 12942142 AGCACTTTGGGAGGCCAAGGCGGGTGGATCACAAGGTCAGGAGATGGAGACCATCCTGGCTAACA AGCACTTTGGGAGGCCAAGGCGGGTGGATCACGAGGTCAGGAGATGGAGACCATCCTGGCTAACA A G CALR Ensembl:ENSG00000179218 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs950069803 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13372413 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_192844,RMVar_hsa_circ_192845,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_192850 24687 RMVar_ID_24687 Human_SNP_ID_658908682 A-to-I Human chr19 + 12942252 12942252 12942252 AGGTGTGGTGGTGGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAAAAGGATGACGTGAA AGGTGTGGTGGTGGGCGCCTGTAGTCCCAGCTCCTCGGGAGGCTGAGGCAAAAGGATGACGTGAA A C CALR Ensembl:ENSG00000179218 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1225853875 Functional Loss SNV dbSNP153 33..33 33 - - - 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_192844,RMVar_hsa_circ_192845,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_192850 24688 RMVar_ID_24688 Human_SNP_ID_658908689 A-to-I Human chr19 + 12942269 12942269 12942269 CCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAAAAGGATGACGTGAACCCGGGAGGCGGAGCTT CCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCGAAAGGATGACGTGAACCCGGGAGGCGGAGCTT A G CALR Ensembl:ENSG00000179218 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1349750327 Functional Loss SNV dbSNP153 33..33 33 - - - 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_192844,RMVar_hsa_circ_192845,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_192850 24689 RMVar_ID_24689 Human_SNP_ID_658908711 A-to-I Human chr19 + 12942328 12942328 12942328 GAGCTTGCAGTGAGCTGAGATCATGCCATTGCACTCCAGCCTGGGTGATAGCGAGACTCTGTCCC GAGCTTGCAGTGAGCTGAGATCATGCCATTGCCCTCCAGCCTGGGTGATAGCGAGACTCTGTCCC A C CALR Ensembl:ENSG00000179218 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs990222898 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23174151 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_192844,RMVar_hsa_circ_192845,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_192850 24690 RMVar_ID_24690 Human_SNP_ID_658908829 A-to-I Human chr19 + 12942688 12942688 12942688 TTGATCTCGGCTCACTGCAGCCTCTGCCTTCCAGGTTCAAGTGATTCTCATGCCTCATCCTCTCG TTGATCTCGGCTCACTGCAGCCTCTGCCTTCCCGGTTCAAGTGATTCTCATGCCTCATCCTCTCG A C CALR Ensembl:ENSG00000179218 Protein coding intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs543081347 Functional Loss SNV dbSNP153 33..33 33 - - - 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_192844,RMVar_hsa_circ_192845,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_192850 24691 RMVar_ID_24691 Human_SNP_ID_658911724 A-to-I Human chr19 + 12950484 12950484 12950484 TGGAGTGCAATGGCGCAATCCCGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGCGATTCTTTT TGGAGTGCAATGGCGCAATCCCGGCTCACTGCGACCTCCGCCTCCCGGGTTCAAGCGATTCTTTT A G RAD23A Ensembl:ENSG00000179262 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs973287035 Functional Loss SNV dbSNP153 33..33 33 - - - 24692 RMVar_ID_24692 Human_SNP_ID_658911769 A-to-I Human chr19 + 12950608 12950608 12950608 TATTTTTAGTAGAGATGGGATTTCACCCTGTTAGCCAGGATGGTCTCAATCTCCTGACCTAATGA TATTTTTAGTAGAGATGGGATTTCACCCTGTTGGCCAGGATGGTCTCAATCTCCTGACCTAATGA A G RAD23A Ensembl:ENSG00000179262 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs932237869 Functional Loss SNV dbSNP153 33..33 33 - - - 24693 RMVar_ID_24693 Human_SNP_ID_658911788 A-to-I Human chr19 + 12950636 12950636 12950636 TGTTAGCCAGGATGGTCTCAATCTCCTGACCTAATGATCTGCCCGCCTTGGCCTCCCAAAGTGCT TGTTAGCCAGGATGGTCTCAATCTCCTGACCTCATGATCTGCCCGCCTTGGCCTCCCAAAGTGCT A C RAD23A Ensembl:ENSG00000179262 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2974753 Functional Loss SNV dbSNP153 33..33 33 - - - 24694 RMVar_ID_24694 Human_SNP_ID_658911789 A-to-I Human chr19 + 12950636 12950636 12950636 TGTTAGCCAGGATGGTCTCAATCTCCTGACCTAATGATCTGCCCGCCTTGGCCTCCCAAAGTGCT TGTTAGCCAGGATGGTCTCAATCTCCTGACCTGATGATCTGCCCGCCTTGGCCTCCCAAAGTGCT A G RAD23A Ensembl:ENSG00000179262 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2974753 Functional Loss SNV dbSNP153 33..33 33 - - - 24695 RMVar_ID_24695 Human_SNP_ID_658911790 A-to-I Human chr19 + 12950636 12950636 12950636 TGTTAGCCAGGATGGTCTCAATCTCCTGACCTAATGATCTGCCCGCCTTGGCCTCCCAAAGTGCT TGTTAGCCAGGATGGTCTCAATCTCCTGACCTTATGATCTGCCCGCCTTGGCCTCCCAAAGTGCT A T RAD23A Ensembl:ENSG00000179262 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2974753 Functional Loss SNV dbSNP153 33..33 33 - - - 24696 RMVar_ID_24696 Human_SNP_ID_658911841 A-to-I Human chr19 + 12950837 12950837 12950837 CCTGTAATCCCAGCACTTTGGGAGGCTAAGGCAGGCAGACCACTTGGTCAGGAGTTTTAGACCAG CCTGTAATCCCAGCACTTTGGGAGGCTAAGGCGGGCAGACCACTTGGTCAGGAGTTTTAGACCAG A G RAD23A Ensembl:ENSG00000179262 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs74181683 Functional Loss SNV dbSNP153 33..33 33 - - - 24697 RMVar_ID_24697 Human_SNP_ID_658911861 A-to-I Human chr19 + 12950917 12950917 12950917 AAAAACTCGTCTCTACTATAAATACAAAAAGTAGCTGAGCATGGCGGCAGGCCACTGTAGTCCCA AAAAACTCGTCTCTACTATAAATACAAAAAGTGGCTGAGCATGGCGGCAGGCCACTGTAGTCCCA A G RAD23A Ensembl:ENSG00000179262 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1348900632 Functional Loss SNV dbSNP153 33..33 33 - - - 24698 RMVar_ID_24698 Human_SNP_ID_658912368 A-to-I Human chr19 + 12952744 12952744 12952744 GTTCATCCAGATGCTGAACGAGCCCCCTGGGGAGCTGGCGGACATCTCAGATGTGGAGGGGGAGG GTTCATCCAGATGCTGAACGAGCCCCCTGGGGGGCTGGCGGACATCTCAGATGTGGAGGGGGAGG A G RAD23A Ensembl:ENSG00000179262 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs771465178 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_513672,Human_RBP_ID_1554919,Human_RBP_ID_6721407,Human_RBP_ID_9293430,Human_RBP_ID_22977670 Human_Splice_Rec_1964434,Human_Splice_Rec_1964466,Human_Splice_Rec_1964492,Human_Splice_Rec_1964522,Human_Splice_Rec_1964542,Human_Splice_Rec_1964548,Human_Splice_Rec_1964549 RMVar_hsa_circ_41260 24699 RMVar_ID_24699 Human_SNP_ID_658955920 A-to-I Human chr19 - 13111985 13111985 13111985 CTCAAAAAGAAAAAAAATAGGCCGGGCGTGGTAGCTCACGCCTGTAATCCCAGCACTTTGGGAAG CTCAAAAAGAAAAAAAATAGGCCGGGCGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAAG T C TRMT1 Ensembl:ENSG00000104907 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1275641252 Functional Loss SNV dbSNP153 33..33 33 - - - 24700 RMVar_ID_24700 Human_SNP_ID_658955963 A-to-I Human chr19 - 13112193 13112148 13112193 CCTGAGGTCAGGACTTTGAGACCAGCTGGCCAACATGGTAAAACCCCATCTCTACTAAAAATACA CCTGAGGTCAGGACTTTGAGACCAGCTGGCCA_________________________________ CCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTTACCATGT C TRMT1 Ensembl:ENSG00000104907 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1384291260 Functional Loss DEL dbSNP153 33..65 33 - - - Human_RBP_ID_22501703 24701 RMVar_ID_24701 Human_SNP_ID_658955969 A-to-I Human chr19 - 13112193 13112193 13112193 CCTGAGGTCAGGACTTTGAGACCAGCTGGCCAACATGGTAAAACCCCATCTCTACTAAAAATACA CCTGAGGTCAGGACTTTGAGACCAGCTGGCCAGCATGGTAAAACCCCATCTCTACTAAAAATACA T C TRMT1 Ensembl:ENSG00000104907 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1408533753 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22501703 24702 RMVar_ID_24702 Human_SNP_ID_658956562 A-to-I Human chr19 - 13114410 13114410 13114410 TGCCCGCCTCGGCCTCCCAAAGTGGTGGGATTATAGGCATGAGCCACTGCACCTGGCTATGCCAG TGCCCGCCTCGGCCTCCCAAAGTGGTGGGATTGTAGGCATGAGCCACTGCACCTGGCTATGCCAG T C TRMT1 Ensembl:ENSG00000104907 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1036965910 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50465,RMVar_hsa_circ_128204,RMVar_hsa_circ_192870 24703 RMVar_ID_24703 Human_SNP_ID_658956615 A-to-I Human chr19 - 13114586 13114586 13114586 GTGATCTTGGCTCACTGCAACCTCCGCCTCCCAGGTTCAAGTGATTCTCCTGCCTTAGCCTCCCG GTGATCTTGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGTGATTCTCCTGCCTTAGCCTCCCG T C TRMT1 Ensembl:ENSG00000104907 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1227228938 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50465,RMVar_hsa_circ_128204,RMVar_hsa_circ_192870 24704 RMVar_ID_24704 Human_SNP_ID_658959548 A-to-I Human chr19 + 13124432 13124432 13124432 CAAAAAAGAAAAAAAAATACTGATGCAAGATGAGGTCTTGCTGTATTGCCCAGGCTGGTCTCAAA CAAAAAAGAAAAAAAAATACTGATGCAAGATGGGGTCTTGCTGTATTGCCCAGGCTGGTCTCAAA A G NACC1 Ensembl:ENSG00000160877 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs902271777 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100302,RMVar_hsa_circ_116017,RMVar_hsa_circ_192873,RMVar_hsa_circ_192874 24705 RMVar_ID_24705 Human_SNP_ID_658960331 A-to-I Human chr19 + 13127240 13127240 13127240 GCTTTGTTGGTCAGACGCAGTGGCTCATGCCTATAATCGCAGGGTTTTGTGAGGCTGTGGCAGGA GCTTTGTTGGTCAGACGCAGTGGCTCATGCCTGTAATCGCAGGGTTTTGTGAGGCTGTGGCAGGA A G NACC1 Ensembl:ENSG00000160877 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1044085300 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13373120 RMVar_hsa_circ_100302,RMVar_hsa_circ_116017,RMVar_hsa_circ_192873,RMVar_hsa_circ_192874 24706 RMVar_ID_24706 Human_SNP_ID_658960733 A-to-I Human chr19 + 13128552 13128552 13128552 TTTGTCCATAGCAGAGCCCTGAGACTGAGCCCAGTCCCCTGGAGGTGAAAACCCTTTCTGGAAGG TTTGTCCATAGCAGAGCCCTGAGACTGAGCCCGGTCCCCTGGAGGTGAAAACCCTTTCTGGAAGG A G NACC1 Ensembl:ENSG00000160877 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs942447833 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6721591,Human_RBP_ID_13373164 RMVar_hsa_circ_100302,RMVar_hsa_circ_116017,RMVar_hsa_circ_192873,RMVar_hsa_circ_192874 24707 RMVar_ID_24707 Human_SNP_ID_658966923 A-to-I Human chr19 - 13149290 13149290 13149290 CTTGTGTCTCAGTCTCCTGAGTAGCTGGGACTACAGGTGCCTGCCACGATACCCGGCTAAGTTTT CTTGTGTCTCAGTCTCCTGAGTAGCTGGGACTGCAGGTGCCTGCCACGATACCCGGCTAAGTTTT T C STX10 Ensembl:ENSG00000104915 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1163956791 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117572,RMVar_hsa_circ_192877 24708 RMVar_ID_24708 Human_SNP_ID_658971026 A-to-I Human chr19 + 13162070 13162070 13162070 CCGGGAGGCGGAGGTTGCAGTGAGCCAAGGTCAAGCCACTTCACTTTAGCCTGGGCGACAGAGCA CCGGGAGGCGGAGGTTGCAGTGAGCCAAGGTCCAGCCACTTCACTTTAGCCTGGGCGACAGAGCA A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1230218817 Functional Loss SNV dbSNP153 33..33 33 - - - 24709 RMVar_ID_24709 Human_SNP_ID_658973293 A-to-I Human chr19 + 13170655 13170655 13170655 TTCTTAGGCCAGGCATGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGTGG TTCTTAGGCCAGGCATGGTGGCTCACGCCTGTGATCCCAGCACTTTGGGAGGCCGAGGCAGGTGG A G HSALNG0124214 RNACentral:URS0000EA9BBD lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs907461106 Functional Loss SNV dbSNP153 33..33 33 - - - 24710 RMVar_ID_24710 Human_SNP_ID_659003473 A-to-I Human chr19 - 13267700 13267700 13267700 GGCCTCAAGCAATCTTCCCAACTCGTCCTCCCAAGGTGCTGGGATTATAGCTGTGAGCCACGGCA GGCCTCAAGCAATCTTCCCAACTCGTCCTCCCGAGGTGCTGGGATTATAGCTGTGAGCCACGGCA T C CACNA1A Ensembl:ENSG00000141837 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1245211566 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100582,RMVar_hsa_circ_265471,RMVar_hsa_circ_192883,RMVar_hsa_circ_45285,RMVar_hsa_circ_106634,RMVar_hsa_circ_192886,RMVar_hsa_circ_321421,RMVar_hsa_circ_37893,RMVar_hsa_circ_15354,RMVar_hsa_circ_267365,RMVar_hsa_circ_11926,RMVar_hsa_circ_39704 24711 RMVar_ID_24711 Human_SNP_ID_659003477 A-to-I Human chr19 - 13267713 13267713 13267713 GTCTCGAACTTCTGGCCTCAAGCAATCTTCCCAACTCGTCCTCCCAAGGTGCTGGGATTATAGCT GTCTCGAACTTCTGGCCTCAAGCAATCTTCCCGACTCGTCCTCCCAAGGTGCTGGGATTATAGCT T C CACNA1A Ensembl:ENSG00000141837 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs989283099 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100582,RMVar_hsa_circ_265471,RMVar_hsa_circ_192883,RMVar_hsa_circ_45285,RMVar_hsa_circ_106634,RMVar_hsa_circ_192886,RMVar_hsa_circ_321421,RMVar_hsa_circ_37893,RMVar_hsa_circ_15354,RMVar_hsa_circ_267365,RMVar_hsa_circ_11926,RMVar_hsa_circ_39704 24712 RMVar_ID_24712 Human_SNP_ID_659123814 A-to-I Human chr19 + 13732713 13732713 13732713 CTCACTGCAACCTCTGCCTTCCCGGTCCAAGCAGCTCTCCTGCCTTAGCCTCCCAGTAGCTGGGA CTCACTGCAACCTCTGCCTTCCCGGTCCAAGCCGCTCTCCTGCCTTAGCCTCCCAGTAGCTGGGA A C CCDC130 Ensembl:ENSG00000104957 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1453118047 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18722955 24713 RMVar_ID_24713 Human_SNP_ID_659124124 A-to-I Human chr19 + 13733959 13733959 13733959 TTGTTTCATTTTATTTTGAGAGGCAGGATCTCACTCTGTCCCCCAGGCTGGAGTACAGTGGTGCA TTGTTTCATTTTATTTTGAGAGGCAGGATCTCGCTCTGTCCCCCAGGCTGGAGTACAGTGGTGCA A G CCDC130 Ensembl:ENSG00000104957 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs767110136 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_513838 24714 RMVar_ID_24714 Human_SNP_ID_659124756 A-to-I Human chr19 + 13736443 13736442 13736444 ACTAAGCCCGGCTAATTTTTGTATTTTTTAGTAGAGACAGTTTTTCTCCATGTTGGCCAGGCTGG ACTAAGCCCGGCTAATTTTTGTATTTTTTAGT__AGACAGTTTTTCTCCATGTTGGCCAGGCTGG TAG T CCDC130 Ensembl:ENSG00000104957 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1434395927 Functional Loss DEL dbSNP153 33..34 33 - - - 24715 RMVar_ID_24715 Human_SNP_ID_659124757 A-to-I Human chr19 + 13736449 13736449 13736449 CCCGGCTAATTTTTGTATTTTTTAGTAGAGACAGTTTTTCTCCATGTTGGCCAGGCTGGTCTTGA CCCGGCTAATTTTTGTATTTTTTAGTAGAGACGGTTTTTCTCCATGTTGGCCAGGCTGGTCTTGA A G CCDC130 Ensembl:ENSG00000104957 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1293535838 Functional Loss SNV dbSNP153 33..33 33 - - - 24716 RMVar_ID_24716 Human_SNP_ID_659128654 A-to-I Human chr19 + 13750344 13750342 13750344 CCGCCTCCCGGTTTGAGCCATTCTCCTGCCTCAGTTTCCCGAGTAGCTGGGATTACAGGCATGCA CCGCCTCCCGGTTTGAGCCATTCTCCTGCCT__GTTTCCCGAGTAGCTGGGATTACAGGCATGCA TCA T CCDC130 Ensembl:ENSG00000104957 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1249453792 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_119527,RMVar_hsa_circ_192913 24717 RMVar_ID_24717 Human_SNP_ID_659128658 A-to-I Human chr19 + 13750356 13750356 13750356 TTGAGCCATTCTCCTGCCTCAGTTTCCCGAGTAGCTGGGATTACAGGCATGCACCATCACACTCG TTGAGCCATTCTCCTGCCTCAGTTTCCCGAGTTGCTGGGATTACAGGCATGCACCATCACACTCG A T CCDC130 Ensembl:ENSG00000104957 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1014651503 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119527,RMVar_hsa_circ_192913 24718 RMVar_ID_24718 Human_SNP_ID_659128741 A-to-I Human chr19 + 13750682 13750682 13750682 AGGAGTTCCAGACTGGCCTGGTCAACACAGTGAAACCCTGTCTCTACTAAAAATACAAAAAAATT AGGAGTTCCAGACTGGCCTGGTCAACACAGTGCAACCCTGTCTCTACTAAAAATACAAAAAAATT A C CCDC130 Ensembl:ENSG00000104957 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1441189689 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119527,RMVar_hsa_circ_192913 24719 RMVar_ID_24719 Human_SNP_ID_659131343 A-to-I Human chr19 + 13759490 13759490 13759490 CATAGACAGAAACAGTAGAAATTTGGCTGGGCACAGTGACTCACGCCTGTAATCCAGCACATTGG CATAGACAGAAACAGTAGAAATTTGGCTGGGCGCAGTGACTCACGCCTGTAATCCAGCACATTGG A G CCDC130 Ensembl:ENSG00000104957 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904312937 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13374051 RMVar_hsa_circ_83736,RMVar_hsa_circ_119527,RMVar_hsa_circ_192913,RMVar_hsa_circ_92602,RMVar_hsa_circ_192915,RMVar_hsa_circ_192919 24720 RMVar_ID_24720 Human_SNP_ID_659131515 A-to-I Human chr19 + 13760012 13760012 13760012 CGGGGTTTCTCCATGTTGGTCAGGCAGGTCTCAAACTCCCATCCTCAGGTTATCTGCCTGCCTCG CGGGGTTTCTCCATGTTGGTCAGGCAGGTCTCGAACTCCCATCCTCAGGTTATCTGCCTGCCTCG A G CCDC130 Ensembl:ENSG00000104957 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490832,GSM3490833,GSM3490834 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 31158229,32596459 RNA-Seq:(High) rs891582556 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83736,RMVar_hsa_circ_119527,RMVar_hsa_circ_192913,RMVar_hsa_circ_92602,RMVar_hsa_circ_192915,RMVar_hsa_circ_192919 24721 RMVar_ID_24721 Human_SNP_ID_659131546 A-to-I Human chr19 + 13760127 13760127 13760127 TTGTGTATTTTTAGTAGAGGCGGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCCAACCT TTGTGTATTTTTAGTAGAGGCGGGGTTTCACCGTGTTGGCCAGGCTGGTCTCGAACTCCCAACCT A G CCDC130 Ensembl:ENSG00000104957 Protein coding intron GSE123020:GSM3490829,GSM3490830,GSM3490831 esophageal squamous carcinoma cells,EC109 cell line - 32596459 RNA-Seq:(High) rs1343641591 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83736,RMVar_hsa_circ_119527,RMVar_hsa_circ_192913,RMVar_hsa_circ_92602,RMVar_hsa_circ_192915,RMVar_hsa_circ_192919 24722 RMVar_ID_24722 Human_SNP_ID_659131669 A-to-I Human chr19 + 13760647 13760647 13760647 ACTGGGTCTCACTCTGTTGCCCAGGCTGGAGTACAGCGGCAAATCATGTCTCACTGCAGCCTCGA ACTGGGTCTCACTCTGTTGCCCAGGCTGGAGTGCAGCGGCAAATCATGTCTCACTGCAGCCTCGA A G CCDC130 Ensembl:ENSG00000104957 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,31158229,32596459 RNA-Seq:(High) rs1013172200 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13374080,Human_RBP_ID_17568948 RMVar_hsa_circ_83736,RMVar_hsa_circ_119527,RMVar_hsa_circ_192913,RMVar_hsa_circ_92602,RMVar_hsa_circ_192915,RMVar_hsa_circ_192919 24723 RMVar_ID_24723 Human_SNP_ID_659131670 A-to-I Human chr19 + 13760647 13760647 13760647 ACTGGGTCTCACTCTGTTGCCCAGGCTGGAGTACAGCGGCAAATCATGTCTCACTGCAGCCTCGA ACTGGGTCTCACTCTGTTGCCCAGGCTGGAGTTCAGCGGCAAATCATGTCTCACTGCAGCCTCGA A T CCDC130 Ensembl:ENSG00000104957 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,31158229,32596459 RNA-Seq:(High) rs1013172200 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13374080,Human_RBP_ID_17568948 RMVar_hsa_circ_83736,RMVar_hsa_circ_119527,RMVar_hsa_circ_192913,RMVar_hsa_circ_92602,RMVar_hsa_circ_192915,RMVar_hsa_circ_192919 24724 RMVar_ID_24724 Human_SNP_ID_659131740 A-to-I Human chr19 + 13760898 13760898 13760898 TCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTCCAGGTTCCCACCACTGTGCATG TCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTGGCTGGGATTCCAGGTTCCCACCACTGTGCATG A G CCDC130 Ensembl:ENSG00000104957 Protein coding intron GSE38233;GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,32596459 RNA-Seq:(High) rs1366447451 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83736,RMVar_hsa_circ_119527,RMVar_hsa_circ_192913,RMVar_hsa_circ_92602,RMVar_hsa_circ_192915,RMVar_hsa_circ_192919 24725 RMVar_ID_24725 Human_SNP_ID_659131746 A-to-I Human chr19 + 13760918 13760918 13760918 AGCCTCCCAAGTAGCTGGGATTCCAGGTTCCCACCACTGTGCATGGCTAATTTTTGTATTTTTAG AGCCTCCCAAGTAGCTGGGATTCCAGGTTCCCGCCACTGTGCATGGCTAATTTTTGTATTTTTAG A G CCDC130 Ensembl:ENSG00000104957 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1326280196 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83736,RMVar_hsa_circ_119527,RMVar_hsa_circ_192913,RMVar_hsa_circ_92602,RMVar_hsa_circ_192915,RMVar_hsa_circ_192919 24726 RMVar_ID_24726 Human_SNP_ID_659131799 A-to-I Human chr19 + 13761118 13761118 13761118 ATGGAACCTCTTGGCTGGGCGCGGTGGCTCACATCTGTAATCCCAGCACTTTGGGAGGCTGAGGC ATGGAACCTCTTGGCTGGGCGCGGTGGCTCACGTCTGTAATCCCAGCACTTTGGGAGGCTGAGGC A G CCDC130 Ensembl:ENSG00000104957 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs572158033 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83736,RMVar_hsa_circ_119527,RMVar_hsa_circ_192913,RMVar_hsa_circ_92602,RMVar_hsa_circ_192915,RMVar_hsa_circ_192919 24727 RMVar_ID_24727 Human_SNP_ID_659131802 A-to-I Human chr19 + 13761130 13761130 13761130 GGCTGGGCGCGGTGGCTCACATCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGCGGATCACG GGCTGGGCGCGGTGGCTCACATCTGTAATCCCGGCACTTTGGGAGGCTGAGGCAGGCGGATCACG A G CCDC130 Ensembl:ENSG00000104957 Protein coding intron GSE38233;GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,32596459 RNA-Seq:(High) rs1423308452 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83736,RMVar_hsa_circ_119527,RMVar_hsa_circ_192913,RMVar_hsa_circ_92602,RMVar_hsa_circ_192915,RMVar_hsa_circ_192919 24728 RMVar_ID_24728 Human_SNP_ID_659131918 A-to-I Human chr19 + 13761619 13761619 13761619 TTTGTGGGATGAGGCCGTGCGTGGTGGCTCACACCTGTAATCCCAGTGCTTTGGGAGGCTCAGGT TTTGTGGGATGAGGCCGTGCGTGGTGGCTCACGCCTGTAATCCCAGTGCTTTGGGAGGCTCAGGT A G CCDC130 Ensembl:ENSG00000104957 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1428086844 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83736,RMVar_hsa_circ_119527,RMVar_hsa_circ_192913,RMVar_hsa_circ_92602,RMVar_hsa_circ_192915,RMVar_hsa_circ_192919 24729 RMVar_ID_24729 Human_SNP_ID_659132042 A-to-I Human chr19 - 13762063 13762063 13762063 AGCCTCCCAAGTATCCAGTACTACAGATGTGCACCACCACGCCCAGCTAATTAAAACATTTATTT AGCCTCCCAAGTATCCAGTACTACAGATGTGCCCCACCACGCCCAGCTAATTAAAACATTTATTT T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1007292949 Functional Loss SNV dbSNP153 33..33 33 - - - 24730 RMVar_ID_24730 Human_SNP_ID_659134930 A-to-I Human chr19 + 13769212 13769212 13769212 TTGAGATGGAGTCTTGCTCTGTCCCTCAGGCTAGAGTGCAGTGGCACGATCTGGGCTCCCTGCAA TTGAGATGGAGTCTTGCTCTGTCCCTCAGGCTGGAGTGCAGTGGCACGATCTGGGCTCCCTGCAA A G MRI1 Ensembl:ENSG00000037757 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1481386282 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 24731 RMVar_ID_24731 Human_SNP_ID_659134934 A-to-I Human chr19 + 13769225 13769225 13769225 TTGCTCTGTCCCTCAGGCTAGAGTGCAGTGGCACGATCTGGGCTCCCTGCAACCTCCACCTCCCG TTGCTCTGTCCCTCAGGCTAGAGTGCAGTGGCGCGATCTGGGCTCCCTGCAACCTCCACCTCCCG A G MRI1 Ensembl:ENSG00000037757 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs755728649 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 24732 RMVar_ID_24732 Human_SNP_ID_659134945 A-to-I Human chr19 + 13769267 13769267 13769267 CTCCCTGCAACCTCCACCTCCCGGGCTCAAGCAGTTCTCCTGCCTCAGCCCCCCAAGTAGCTGGG CTCCCTGCAACCTCCACCTCCCGGGCTCAAGCGGTTCTCCTGCCTCAGCCCCCCAAGTAGCTGGG A G MRI1 Ensembl:ENSG00000037757 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs949006707 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 24733 RMVar_ID_24733 Human_SNP_ID_659134961 A-to-I Human chr19 + 13769303 13769303 13769303 CTCCTGCCTCAGCCCCCCAAGTAGCTGGGACTATAGGTGGGTGCCACCACGCCTGGCTAATTTTT CTCCTGCCTCAGCCCCCCAAGTAGCTGGGACTGTAGGTGGGTGCCACCACGCCTGGCTAATTTTT A G MRI1 Ensembl:ENSG00000037757 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1162740719 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 24734 RMVar_ID_24734 Human_SNP_ID_659135151 A-to-I Human chr19 + 13770001 13770001 13770001 TTTGTTTATTTTCATAGAGATAGGGTCTCGCTATGTTCCCCAGGCTGGTCTCAAACTCCTGGCCT TTTGTTTATTTTCATAGAGATAGGGTCTCGCTGTGTTCCCCAGGCTGGTCTCAAACTCCTGGCCT A G MRI1 Ensembl:ENSG00000037757 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs143186034 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 24735 RMVar_ID_24735 Human_SNP_ID_659135882 A-to-I Human chr19 + 13772557 13772557 13772557 CATTTATAAAATGTGGATAACAGGCCGGGCGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGG CATTTATAAAATGTGGATAACAGGCCGGGCGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGG A G MRI1 Ensembl:ENSG00000037757 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1159584299 Functional Loss SNV dbSNP153 33..33 33 - - - 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 24736 RMVar_ID_24736 Human_SNP_ID_659135884 A-to-I Human chr19 + 13772567 13772567 13772567 ATGTGGATAACAGGCCGGGCGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGC ATGTGGATAACAGGCCGGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGC A G MRI1 Ensembl:ENSG00000037757 Protein coding 3'UTR GSE47997;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,29129909,31158229,31158229,31158229 RNA-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 24737 RMVar_ID_24737 Human_SNP_ID_659135886 A-to-I Human chr19 + 13772573 13772573 13772573 ATAACAGGCCGGGCGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGTGG ATAACAGGCCGGGCGCAGTGGCTCACACCTGTGATCCCAGCACTTTGGGAGGCCGAGGCAGGTGG A G MRI1 Ensembl:ENSG00000037757 Protein coding 3'UTR GSE47997;GSE38233;GSE38233;GSE100210;GSE100210;GSE99789;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;cultured B-cells;cultured B-cells;HepG2 cell line;HepG2 cell line;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,24183664,24183664,29129909,29129909,29796672,29796672,31158229,31158229,31158229,31158229,31158229 RNA-Seq:(High) rs1434154794 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 24738 RMVar_ID_24738 Human_SNP_ID_659135901 A-to-I Human chr19 + 13772617 13772617 13772617 TTGGGAGGCCGAGGCAGGTGGATCACAAGATCAGGAGATTGAGACCATCCTGGCTAACATGGTGA TTGGGAGGCCGAGGCAGGTGGATCACAAGATCGGGAGATTGAGACCATCCTGGCTAACATGGTGA A G MRI1 Ensembl:ENSG00000037757 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,31158229,31158229,31158229 RNA-Seq:(High) rs1342386386 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 24739 RMVar_ID_24739 Human_SNP_ID_659135929 A-to-I Human chr19 + 13772734 13772734 13772734 CCTGCAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATGGCGTGAAACTGGGAGGCAGAGCTT CCTGCAGTCCCAGCTACTTGGGAGGCTGAGGCGGGAGAATGGCGTGAAACTGGGAGGCAGAGCTT A G MRI1 Ensembl:ENSG00000037757 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-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 24740 RMVar_ID_24740 Human_SNP_ID_659135935 A-to-I Human chr19 + 13772760 13772760 13772760 TGAGGCAGGAGAATGGCGTGAAACTGGGAGGCAGAGCTTGCAGTGAGCCGAGATAGCGCCACTGC TGAGGCAGGAGAATGGCGTGAAACTGGGAGGCGGAGCTTGCAGTGAGCCGAGATAGCGCCACTGC A G MRI1 Ensembl:ENSG00000037757 Protein coding 3'UTR GSE38233;GSE100210;GSE107867;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,30559470,31158229 RNA-Seq:(High) rs1398159663 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 24741 RMVar_ID_24741 Human_SNP_ID_659136030 A-to-I Human chr19 + 13773078 13773078 13773078 TTACCCAGGCTGGAATGTAGAGGCGAGATCTCAGCTCACTGAAACCTGTGCCTCCCCGGTTCAAG TTACCCAGGCTGGAATGTAGAGGCGAGATCTCGGCTCACTGAAACCTGTGCCTCCCCGGTTCAAG A G MRI1 Ensembl:ENSG00000037757 Protein coding 3'UTR GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,29796672,31158229,31158229,31158229,32596459 RNA-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 24742 RMVar_ID_24742 Human_SNP_ID_659136050 A-to-I Human chr19 + 13773138 13773138 13773138 TCAAGCGATTCTCCTGCCACAGCCTCCTGAGTAGCTGGGATTACAGGCATGCGCCACCATGCCCA TCAAGCGATTCTCCTGCCACAGCCTCCTGAGTTGCTGGGATTACAGGCATGCGCCACCATGCCCA A T MRI1 Ensembl:ENSG00000037757 Protein coding 3'UTR GSE38233;GSE107867 cultured B-cells;ASD brains,Fragile X samples from NIH NeuroBioBank - 24183664,30559470 RNA-Seq:(High) rs765954125 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 24743 RMVar_ID_24743 Human_SNP_ID_659136064 A-to-I Human chr19 + 13773183 13773183 13773183 GGCATGCGCCACCATGCCCAGCTAATTTTTCTATTTTTAGTAGAGACATGATTTCACCATGTTGG GGCATGCGCCACCATGCCCAGCTAATTTTTCTGTTTTTAGTAGAGACATGATTTCACCATGTTGG A G MRI1 Ensembl:ENSG00000037757 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1462697972 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9909176,Human_RBP_ID_25385035 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 24744 RMVar_ID_24744 Human_SNP_ID_659136065 A-to-I Human chr19 + 13773189 13773189 13773189 CGCCACCATGCCCAGCTAATTTTTCTATTTTTAGTAGAGACATGATTTCACCATGTTGGCCAGGC CGCCACCATGCCCAGCTAATTTTTCTATTTTTGGTAGAGACATGATTTCACCATGTTGGCCAGGC A G MRI1 Ensembl:ENSG00000037757 Protein coding 3'UTR GSE38233;GSE100210;GSE107867;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;ASD brains,frontal_cortex;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,30559470,31158229 RNA-Seq:(High) rs1018690292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4504095,Human_RBP_ID_26464902 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 24745 RMVar_ID_24745 Human_SNP_ID_659136068 A-to-I Human chr19 + 13773209 13773209 13773209 TTTTCTATTTTTAGTAGAGACATGATTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACTC TTTTCTATTTTTAGTAGAGACATGATTTCACCGTGTTGGCCAGGCTGGTCTCGAACTCCTGACTC A G MRI1 Ensembl:ENSG00000037757 Protein coding 3'UTR GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,29796672,31158229 RNA-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 24746 RMVar_ID_24746 Human_SNP_ID_659136083 A-to-I Human chr19 + 13773260 13773260 13773260 CGAACTCCTGACTCAAATGATCCCCCTGCCTCAGCCTCCCAAAGTGCTGGGACTACAGGCATGAG CGAACTCCTGACTCAAATGATCCCCCTGCCTCGGCCTCCCAAAGTGCTGGGACTACAGGCATGAG A G MRI1 Ensembl:ENSG00000037757 Protein coding 3'UTR GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,29796672,31158229,31158229,32596459 RNA-Seq:(High) rs1480774123 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 24747 RMVar_ID_24747 Human_SNP_ID_659136086 A-to-I Human chr19 + 13773268 13773268 13773268 TGACTCAAATGATCCCCCTGCCTCAGCCTCCCAAAGTGCTGGGACTACAGGCATGAGCCACTGTG TGACTCAAATGATCCCCCTGCCTCAGCCTCCCGAAGTGCTGGGACTACAGGCATGAGCCACTGTG A G MRI1 Ensembl:ENSG00000037757 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,31158229,32596459 RNA-Seq:(High) rs1017763059 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 24748 RMVar_ID_24748 Human_SNP_ID_659136105 A-to-I Human chr19 + 13773362 13773361 13773362 TCAAAATTAATGCAAAAATCCATGATGAGGCCAGGCTTGGTGGCTCATGCCTGTAATTCCAGCAC TCAAAATTAATGCAAAAATCCATGATGAGGCC_GGCTTGGTGGCTCATGCCTGTAATTCCAGCAC CA C MRI1 Ensembl:ENSG00000037757 Protein coding 3'UTR GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,29796672,31158229 RNA-Seq:(High) rs1196918944 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_13374359,Human_RBP_ID_23174262,Human_RBP_ID_26464905 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 24749 RMVar_ID_24749 Human_SNP_ID_659136110 A-to-I Human chr19 + 13773384 13773384 13773384 TGATGAGGCCAGGCTTGGTGGCTCATGCCTGTAATTCCAGCACTTTGGGAGGATCCCTTGAGCCC TGATGAGGCCAGGCTTGGTGGCTCATGCCTGTGATTCCAGCACTTTGGGAGGATCCCTTGAGCCC A G MRI1 Ensembl:ENSG00000037757 Protein coding 3'UTR GSE38233;GSE100210;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,29129909,31158229,31158229,31158229,32596459 RNA-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 24750 RMVar_ID_24750 Human_SNP_ID_659136124 A-to-I Human chr19 + 13773445 13773445 13773445 GCCCAGGTGTTTGAGACCAGTTTGGGTAACATAGGAAGAGCTTGTCTCTACAAACAAAAATTTAA GCCCAGGTGTTTGAGACCAGTTTGGGTAACATGGGAAGAGCTTGTCTCTACAAACAAAAATTTAA A G MRI1 Ensembl:ENSG00000037757 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs3179532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17567967,Human_RBP_ID_17915599,Human_RBP_ID_23174265,Human_RBP_ID_26472110 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 24751 RMVar_ID_24751 Human_SNP_ID_659136135 A-to-I Human chr19 + 13773494 13773494 13773494 ACAAACAAAAATTTAAAAACAATGAGCTGGGCATGGAACTCACACCTCTAGCCCCAGCTACTCAG ACAAACAAAAATTTAAAAACAATGAGCTGGGCGTGGAACTCACACCTCTAGCCCCAGCTACTCAG A G MRI1 Ensembl:ENSG00000037757 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444839852 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1554995,Human_RBP_ID_13374362,Human_RBP_ID_17915601,Human_RBP_ID_26464908 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 24752 RMVar_ID_24752 Human_SNP_ID_659136144 A-to-I Human chr19 + 13773521 13773520 13773522 TGGGCATGGAACTCACACCTCTAGCCCCAGCTACTCAGGCTGAAGTGGGAGGATGGCTTGAGCCC TGGGCATGGAACTCACACCTCTAGCCCCAGCT__TCAGGCTGAAGTGGGAGGATGGCTTGAGCCC TAC T MRI1 Ensembl:ENSG00000037757 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900284774 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_513860,Human_RBP_ID_26464908 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 24753 RMVar_ID_24753 Human_SNP_ID_659136145 A-to-I Human chr19 + 13773521 13773521 13773521 TGGGCATGGAACTCACACCTCTAGCCCCAGCTACTCAGGCTGAAGTGGGAGGATGGCTTGAGCCC TGGGCATGGAACTCACACCTCTAGCCCCAGCTCCTCAGGCTGAAGTGGGAGGATGGCTTGAGCCC A C MRI1 Ensembl:ENSG00000037757 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054511975 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_513860,Human_RBP_ID_26464908 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 24754 RMVar_ID_24754 Human_SNP_ID_659136147 A-to-I Human chr19 + 13773525 13773525 13773525 CATGGAACTCACACCTCTAGCCCCAGCTACTCAGGCTGAAGTGGGAGGATGGCTTGAGCCCAGGA CATGGAACTCACACCTCTAGCCCCAGCTACTCCGGCTGAAGTGGGAGGATGGCTTGAGCCCAGGA A C MRI1 Ensembl:ENSG00000037757 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1138208 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_513860,Human_RBP_ID_13374368,Human_RBP_ID_26464908 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 24755 RMVar_ID_24755 Human_SNP_ID_659136148 A-to-I Human chr19 + 13773531 13773531 13773531 ACTCACACCTCTAGCCCCAGCTACTCAGGCTGAAGTGGGAGGATGGCTTGAGCCCAGGAGTTCAA ACTCACACCTCTAGCCCCAGCTACTCAGGCTGTAGTGGGAGGATGGCTTGAGCCCAGGAGTTCAA A T MRI1 Ensembl:ENSG00000037757 Protein coding 3'UTR GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;ASD brains,cerebellum;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,30559470,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs1486644092 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_513860,Human_RBP_ID_13374368,Human_RBP_ID_26464909 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 24756 RMVar_ID_24756 Human_SNP_ID_659136157 A-to-I Human chr19 + 13773562 13773562 13773562 GAAGTGGGAGGATGGCTTGAGCCCAGGAGTTCAAGGATGCAGTGTGCTTTGATTGCACTACTGCA GAAGTGGGAGGATGGCTTGAGCCCAGGAGTTCGAGGATGCAGTGTGCTTTGATTGCACTACTGCA A G MRI1 Ensembl:ENSG00000037757 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1022096919 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_513860,Human_RBP_ID_13374369 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 24757 RMVar_ID_24757 Human_SNP_ID_659136162 A-to-I Human chr19 + 13773594 13773594 13773594 AAGGATGCAGTGTGCTTTGATTGCACTACTGCACTTCACCCTAAGCAACAGAGTGAGACCCCATC AAGGATGCAGTGTGCTTTGATTGCACTACTGCGCTTCACCCTAAGCAACAGAGTGAGACCCCATC A G MRI1 Ensembl:ENSG00000037757 Protein coding 3'UTR GSE47997;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1374307800 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26464910 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 24758 RMVar_ID_24758 Human_SNP_ID_659136165 A-to-I Human chr19 + 13773604 13773604 13773604 TGTGCTTTGATTGCACTACTGCACTTCACCCTAAGCAACAGAGTGAGACCCCATCTCTTTAAAAA TGTGCTTTGATTGCACTACTGCACTTCACCCTGAGCAACAGAGTGAGACCCCATCTCTTTAAAAA A G MRI1 Ensembl:ENSG00000037757 Protein coding 3'UTR GSE47997;GSE38233;GSE38233;GSE100210;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;cultured B-cells;HepG2 cell line;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,24183664,29129909,29129909,31158229,31158229,31158229,31158229,31158229,31158229,32596459,32596459 RNA-Seq:(High) rs1241246013 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26464910 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 24759 RMVar_ID_24759 Human_SNP_ID_659136217 A-to-I Human chr19 + 13773775 13773775 13773775 CGCCTTCTGGGTTCAAGCGACTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGAGCCTG CGCCTTCTGGGTTCAAGCGACTCTCCTGCCTCCGCCTCCCGAGTAGCTGGGATTACAGGAGCCTG A C MRI1 Ensembl:ENSG00000037757 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs557919261 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13374371 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 24760 RMVar_ID_24760 Human_SNP_ID_659136222 A-to-I Human chr19 + 13773797 13773797 13773797 CTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGAGCCTGGCACTATGCCTGGCTAATTTTT CTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTGCAGGAGCCTGGCACTATGCCTGGCTAATTTTT A G MRI1 Ensembl:ENSG00000037757 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1139803 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 24761 RMVar_ID_24761 Human_SNP_ID_659136235 A-to-I Human chr19 + 13773855 13773855 13773855 AATTTTTGTATTTTTATTGGAGACACCATGTTAGTCGTGGCTGGTCTCCAACTCCTGACCTCGGG AATTTTTGTATTTTTATTGGAGACACCATGTTGGTCGTGGCTGGTCTCCAACTCCTGACCTCGGG A G MRI1 Ensembl:ENSG00000037757 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-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 24762 RMVar_ID_24762 Human_SNP_ID_659136239 A-to-I Human chr19 + 13773872 13773872 13773872 TGGAGACACCATGTTAGTCGTGGCTGGTCTCCAACTCCTGACCTCGGGTGATCCGCGCCCCGCGG TGGAGACACCATGTTAGTCGTGGCTGGTCTCCGACTCCTGACCTCGGGTGATCCGCGCCCCGCGG A G MRI1 Ensembl:ENSG00000037757 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1222536608 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13374373,Human_RBP_ID_23174268,Human_RBP_ID_23783393,Human_RBP_ID_26472111 Human_miRNA_ID_135184 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 24763 RMVar_ID_24763 Human_SNP_ID_659136257 A-to-I Human chr19 + 13773925 13773925 13773925 CGCGCCCCGCGGCCTCCGAAAGTGCTGGGATTACAAGCGTGAGCCACCGTGCCCGGCCTAAATAA CGCGCCCCGCGGCCTCCGAAAGTGCTGGGATTGCAAGCGTGAGCCACCGTGCCCGGCCTAAATAA A G MRI1 Ensembl:ENSG00000037757 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-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 24764 RMVar_ID_24764 Human_SNP_ID_659136259 A-to-I Human chr19 + 13773927 13773927 13773927 CGCCCCGCGGCCTCCGAAAGTGCTGGGATTACAAGCGTGAGCCACCGTGCCCGGCCTAAATAAAA CGCCCCGCGGCCTCCGAAAGTGCTGGGATTACCAGCGTGAGCCACCGTGCCCGGCCTAAATAAAA A C MRI1 Ensembl:ENSG00000037757 Protein coding 3'UTR GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-Seq:(High) rs1006510765 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 24765 RMVar_ID_24765 Human_SNP_ID_659137971 A-to-I Human chr19 + 13779092 13779092 13779092 GCAGTCGTCCTGCCTTGGCCTCCCAGAGTGCTAGGATTACAGGTGTGATCCACCATGCCCCACAA GCAGTCGTCCTGCCTTGGCCTCCCAGAGTGCTGGGATTACAGGTGTGATCCACCATGCCCCACAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs754360038 Functional Loss SNV dbSNP153 33..33 33 - - - 24766 RMVar_ID_24766 Human_SNP_ID_659142507 A-to-I Human chr19 - 13794359 13794359 13794359 TCGGCTCACTGCAACCTGCGCCTCCCGGGGTCAAGTGATTCTCCTGCCTCAGCCTCCCGAATAGC TCGGCTCACTGCAACCTGCGCCTCCCGGGGTCGAGTGATTCTCCTGCCTCAGCCTCCCGAATAGC T C lnc-C19orf57-8 RNACentral:URS0000D574CD lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1401658469 Functional Loss SNV dbSNP153 33..33 33 - - - 24767 RMVar_ID_24767 Human_SNP_ID_659144451 A-to-I Human chr19 + 13800405 13800405 13800405 CTCCTGCCTCAGCCTCCCAAGTAGCCGGGACTACAGGCGCCCGCCACCAAGCCCGGCTAATTTTT CTCCTGCCTCAGCCTCCCAAGTAGCCGGGACTCCAGGCGCCCGCCACCAAGCCCGGCTAATTTTT A C ZSWIM4 Ensembl:ENSG00000132003 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs925592500 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38419,RMVar_hsa_circ_72822 24768 RMVar_ID_24768 Human_SNP_ID_659144455 A-to-I Human chr19 + 13800421 13800421 13800421 CCAAGTAGCCGGGACTACAGGCGCCCGCCACCAAGCCCGGCTAATTTTTTGTATTTTTAGTAGAG CCAAGTAGCCGGGACTACAGGCGCCCGCCACCGAGCCCGGCTAATTTTTTGTATTTTTAGTAGAG A G ZSWIM4 Ensembl:ENSG00000132003 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1305690960 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38419,RMVar_hsa_circ_72822 24769 RMVar_ID_24769 Human_SNP_ID_659144665 A-to-I Human chr19 + 13801087 13801087 13801087 ATCGCTTTTGCCCGAGAGGTCGAGCCTGCAGTAAGCTATGATTGCACCACCGTACTCCAGCCTGG ATCGCTTTTGCCCGAGAGGTCGAGCCTGCAGTGAGCTATGATTGCACCACCGTACTCCAGCCTGG A G ZSWIM4 Ensembl:ENSG00000132003 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1261825604 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13374534 RMVar_hsa_circ_38419,RMVar_hsa_circ_72822 24770 RMVar_ID_24770 Human_SNP_ID_659145113 A-to-I Human chr19 + 13802610 13802610 13802610 TCAAAAGAAAAAAAAAAGGGAGATAGGGTCTCACTCTGTTGCCCAGGCTGGAGTGCAGTGGCGCG TCAAAAGAAAAAAAAAAGGGAGATAGGGTCTCGCTCTGTTGCCCAGGCTGGAGTGCAGTGGCGCG A G ZSWIM4 Ensembl:ENSG00000132003 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1265466592 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38419,RMVar_hsa_circ_72822 24771 RMVar_ID_24771 Human_SNP_ID_659145144 A-to-I Human chr19 + 13802744 13802744 13802744 GGTACCACAGGCGCAGGCCACCACACTTGACTAGTTTTTAAGTTTTTTGTAGAGACCTGGTCTCA GGTACCACAGGCGCAGGCCACCACACTTGACTCGTTTTTAAGTTTTTTGTAGAGACCTGGTCTCA A C ZSWIM4 Ensembl:ENSG00000132003 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1429672841 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38419,RMVar_hsa_circ_72822 24772 RMVar_ID_24772 Human_SNP_ID_659145318 A-to-I Human chr19 + 13803524 13803517 13803533 AAGTGTTGGGCTGGGCTCGGTGGCTCGCGCCTATAATCCCAGCACTTTGGGAGGCCGAGGCGGGT AAGTGTTGGGCTGGGCTCGGTGGCTAGCGCCTATAATCCCAACACTTTGGGAGGCCGAGGCGGGT CGCGCCTATAATCCCAG AGCGCCTATAATCCCAA ZSWIM4 Ensembl:ENSG00000132003 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs386807018 Functional Loss MNV dbSNP153 26..42 33 - - - RMVar_hsa_circ_38419,RMVar_hsa_circ_72822 24773 RMVar_ID_24773 Human_SNP_ID_659145630 A-to-I Human chr19 + 13804610 13804610 13804610 CGGAGGTTGCAGTGAGCCCAGGTCGCAGCACTACACTCCAGCCTGGGCCACAGAGCGAGATTTTG CGGAGGTTGCAGTGAGCCCAGGTCGCAGCACTGCACTCCAGCCTGGGCCACAGAGCGAGATTTTG A G ZSWIM4 Ensembl:ENSG00000132003 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs921433629 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38419,RMVar_hsa_circ_72822 24774 RMVar_ID_24774 Human_SNP_ID_659147143 A-to-I Human chr19 + 13809810 13809802 13809810 CCTACATGTTTTGTTTCTTTTTTTCTTTTTTTAGAGACAGGATCTCACTGTGCGCCCAGGCTGAA CCTACATGTTTTGTTTCTTTTTTTC________GAGACAGGATCTCACTGTGCGCCCAGGCTGAA CTTTTTTTA C ZSWIM4 Ensembl:ENSG00000132003 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs920051515 Functional Loss DEL dbSNP153 26..33 33 - - - RMVar_hsa_circ_72822,RMVar_hsa_circ_21621 24775 RMVar_ID_24775 Human_SNP_ID_659147144 A-to-I Human chr19 + 13809810 13809810 13809810 CCTACATGTTTTGTTTCTTTTTTTCTTTTTTTAGAGACAGGATCTCACTGTGCGCCCAGGCTGAA CCTACATGTTTTGTTTCTTTTTTTCTTTTTTTCGAGACAGGATCTCACTGTGCGCCCAGGCTGAA A C ZSWIM4 Ensembl:ENSG00000132003 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs529167596 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72822,RMVar_hsa_circ_21621 24776 RMVar_ID_24776 Human_SNP_ID_659147434 A-to-I Human chr19 + 13810759 13810759 13810759 AGCCTCCCGAGTAGCTGGGACTACAGAGGCCCACCACCACGCCCGGCTAATTTTTTTGTATTTTT AGCCTCCCGAGTAGCTGGGACTACAGAGGCCCGCCACCACGCCCGGCTAATTTTTTTGTATTTTT A G ZSWIM4 Ensembl:ENSG00000132003 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1198388768 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72822,RMVar_hsa_circ_21621 24777 RMVar_ID_24777 Human_SNP_ID_659148856 A-to-I Human chr19 + 13815672 13815672 13815672 TTTTGTGTTTTTAGTAGAGATGGGGTTTCACTATGTTGGCCAGGCTCTTCTCGAACTCCTGACCT TTTTGTGTTTTTAGTAGAGATGGGGTTTCACTGTGTTGGCCAGGCTCTTCTCGAACTCCTGACCT A G ZSWIM4 Ensembl:ENSG00000132003 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1412953068 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72822,RMVar_hsa_circ_45264,RMVar_hsa_circ_21621,RMVar_hsa_circ_53321,RMVar_hsa_circ_353580 24778 RMVar_ID_24778 Human_SNP_ID_659149067 A-to-I Human chr19 + 13816496 13816496 13816496 AAATCCAAAACAAATTAGCCAGGTGTGGTGGCACGTACCTGTATTCCCAGCTACTCAGGACACTG AAATCCAAAACAAATTAGCCAGGTGTGGTGGCGCGTACCTGTATTCCCAGCTACTCAGGACACTG A G ZSWIM4 Ensembl:ENSG00000132003 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs887191796 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17190563 RMVar_hsa_circ_72822,RMVar_hsa_circ_45264,RMVar_hsa_circ_21621,RMVar_hsa_circ_53321,RMVar_hsa_circ_353580 24779 RMVar_ID_24779 Human_SNP_ID_659150512 A-to-I Human chr19 + 13821411 13821411 13821411 AAACAACTTGGGATCCAGCCTGGTACACATCTATGGTCCTAGCTACTTGGGAGGCTGAGGAGGGA AAACAACTTGGGATCCAGCCTGGTACACATCTGTGGTCCTAGCTACTTGGGAGGCTGAGGAGGGA A G ZSWIM4 Ensembl:ENSG00000132003 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1045211312 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72822,RMVar_hsa_circ_45264,RMVar_hsa_circ_353580,RMVar_hsa_circ_28416,RMVar_hsa_circ_56786,RMVar_hsa_circ_45954,RMVar_hsa_circ_345484,RMVar_hsa_circ_333666,RMVar_hsa_circ_192935,RMVar_hsa_circ_192936 24780 RMVar_ID_24780 Human_SNP_ID_659150857 A-to-I Human chr19 + 13822722 13822722 13822722 AAAATTAGGGCCAGGAGCCATGGTTCACGCCTATAATCCCAGTACTTTGGGAGGCCGAGGAGGGC AAAATTAGGGCCAGGAGCCATGGTTCACGCCTGTAATCCCAGTACTTTGGGAGGCCGAGGAGGGC A G ZSWIM4 Ensembl:ENSG00000132003 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs771197441 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72822,RMVar_hsa_circ_45264,RMVar_hsa_circ_353580,RMVar_hsa_circ_28416,RMVar_hsa_circ_56786,RMVar_hsa_circ_45954,RMVar_hsa_circ_345484,RMVar_hsa_circ_333666,RMVar_hsa_circ_192935,RMVar_hsa_circ_192936 24781 RMVar_ID_24781 Human_SNP_ID_659155488 A-to-I Human chr19 - 13838380 13838380 13838380 TTTTTAAACTTGTTTTTGTTTATTTTAGAGATAGGGTCTTGCTCTGTCACTTAGGCTGGAGTTCA TTTTTAAACTTGTTTTTGTTTATTTTAGAGATGGGGTCTTGCTCTGTCACTTAGGCTGGAGTTCA T C AC020916.1 Ensembl:ENSG00000267519 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1274977951 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13544713 24782 RMVar_ID_24782 Human_SNP_ID_659155572 A-to-I Human chr19 - 13838679 13838679 13838679 TGCTAGCCAGGTGTTGGGCTCTTATCAAAAGAAGCTCCACTCACTAAAGACTTAGGGCTGGCTTC TGCTAGCCAGGTGTTGGGCTCTTATCAAAAGAGGCTCCACTCACTAAAGACTTAGGGCTGGCTTC T C AC020916.1 Ensembl:ENSG00000267519 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs173189 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2573482 24783 RMVar_ID_24783 Human_SNP_ID_659155573 A-to-I Human chr19 - 13838679 13838679 13838679 TGCTAGCCAGGTGTTGGGCTCTTATCAAAAGAAGCTCCACTCACTAAAGACTTAGGGCTGGCTTC TGCTAGCCAGGTGTTGGGCTCTTATCAAAAGACGCTCCACTCACTAAAGACTTAGGGCTGGCTTC T G AC020916.1 Ensembl:ENSG00000267519 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs173189 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2573482 24784 RMVar_ID_24784 Human_SNP_ID_659177574 A-to-I Human chr19 + 13914210 13914210 13914210 TTTTTTAATTCTTTGAGACAGGGTCTTACTCCATCACCCAGGCTGGAGTGCAGTGATGTGATCAT TTTTTTAATTCTTTGAGACAGGGTCTTACTCCGTCACCCAGGCTGGAGTGCAGTGATGTGATCAT A G CC2D1A Ensembl:ENSG00000132024 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs895778546 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55614,RMVar_hsa_circ_192942,RMVar_hsa_circ_116955 24785 RMVar_ID_24785 Human_SNP_ID_659177584 A-to-I Human chr19 + 13914248 13914248 13914248 CAGGCTGGAGTGCAGTGATGTGATCATAGCTCAGTGTAGCCTCAACCTCCTGGGCTCAAGGGATC CAGGCTGGAGTGCAGTGATGTGATCATAGCTCGGTGTAGCCTCAACCTCCTGGGCTCAAGGGATC A G CC2D1A Ensembl:ENSG00000132024 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1004468328 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55614,RMVar_hsa_circ_192942,RMVar_hsa_circ_116955 24786 RMVar_ID_24786 Human_SNP_ID_659177700 A-to-I Human chr19 + 13914753 13914753 13914753 TGCCTCCCAGGCTCAAGCAATCCTCCCGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCATATG TGCCTCCCAGGCTCAAGCAATCCTCCCGCCTCGGCCTCCTGAGTAGCTGGGATTACAGGCATATG A G CC2D1A Ensembl:ENSG00000132024 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1050526306 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55614,RMVar_hsa_circ_192942,RMVar_hsa_circ_116955 24787 RMVar_ID_24787 Human_SNP_ID_659177847 A-to-I Human chr19 + 13915429 13915429 13915429 CACCAAGCCCGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGCTGCCCAGGC CACCAAGCCCGGCTAATTTTTGTATTTTTAGTGGAGACGGGGTTTCACCATGTTGCTGCCCAGGC A G CC2D1A Ensembl:ENSG00000132024 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1357230006 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55614,RMVar_hsa_circ_192942,RMVar_hsa_circ_116955 24788 RMVar_ID_24788 Human_SNP_ID_659177855 A-to-I Human chr19 + 13915446 13915446 13915446 TTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGCTGCCCAGGCTGGTCTCGAACTCCTGA TTTTGTATTTTTAGTAGAGACGGGGTTTCACCGTGTTGCTGCCCAGGCTGGTCTCGAACTCCTGA A G CC2D1A Ensembl:ENSG00000132024 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1387981722 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55614,RMVar_hsa_circ_192942,RMVar_hsa_circ_116955 24789 RMVar_ID_24789 Human_SNP_ID_659177875 A-to-I Human chr19 + 13915508 13915507 13915509 TGACCTCAGGTGATCCGCCTGCTCCGCCTCCCAAAGTGCGGGGATTACAGGCGTGAGCCACCACC TGACCTCAGGTGATCCGCCTGCTCCGCCTCCC__AGTGCGGGGATTACAGGCGTGAGCCACCACC CAA C CC2D1A Ensembl:ENSG00000132024 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355605141 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_55614,RMVar_hsa_circ_192942,RMVar_hsa_circ_116955 24790 RMVar_ID_24790 Human_SNP_ID_659177915 A-to-I Human chr19 + 13915697 13915697 13915697 ACATAAAAATTAAGAAATTAGCCGGGTGTGGTAGTGCATGCCTTTAGTCCCAGCTCCTCGAGAAG ACATAAAAATTAAGAAATTAGCCGGGTGTGGTGGTGCATGCCTTTAGTCCCAGCTCCTCGAGAAG A G CC2D1A Ensembl:ENSG00000132024 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1320125410 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55614,RMVar_hsa_circ_192942,RMVar_hsa_circ_116955 24791 RMVar_ID_24791 Human_SNP_ID_659177925 A-to-I Human chr19 + 13915756 13915756 13915756 GAGAAGCTGAGGTGGGAGGTTCGCTTGAGTCCAGGAGTTCAAGGCTGCAGTGAGCCGTGATCGTG GAGAAGCTGAGGTGGGAGGTTCGCTTGAGTCCGGGAGTTCAAGGCTGCAGTGAGCCGTGATCGTG A G CC2D1A Ensembl:ENSG00000132024 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs551135650 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55614,RMVar_hsa_circ_192942,RMVar_hsa_circ_116955 24792 RMVar_ID_24792 Human_SNP_ID_659178243 A-to-I Human chr19 + 13917291 13917291 13917291 CAGGAGTTTGAGACTAGCCTGGACAACATAGTAAGACCCCATCTCTACAAAAAAAAATAAAAAAC CAGGAGTTTGAGACTAGCCTGGACAACATAGTTAGACCCCATCTCTACAAAAAAAAATAAAAAAC A T CC2D1A Ensembl:ENSG00000132024 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1315733721 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55614,RMVar_hsa_circ_192942,RMVar_hsa_circ_116955 24793 RMVar_ID_24793 Human_SNP_ID_659179742 A-to-I Human chr19 + 13922211 13922211 13922211 TTTAGTAGAGATGGGGTTTCACTATGTTGGCCAGGCTGGGCTTGAACTCCTGACCTCAGGCAATC TTTAGTAGAGATGGGGTTTCACTATGTTGGCCGGGCTGGGCTTGAACTCCTGACCTCAGGCAATC A G CC2D1A Ensembl:ENSG00000132024 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs943237324 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107714,RMVar_hsa_circ_192942,RMVar_hsa_circ_116955,RMVar_hsa_circ_101859,RMVar_hsa_circ_192943,RMVar_hsa_circ_298286,RMVar_hsa_circ_192945,RMVar_hsa_circ_192946 24794 RMVar_ID_24794 Human_SNP_ID_659194421 A-to-I Human chr19 - 13968062 13968062 13968062 TTTAGGAGAGATGGGGTTTCACCATCTTGGCTAGGCTGGTCTCGAACTCCTGACCTGAAGTGATC TTTAGGAGAGATGGGGTTTCACCATCTTGGCTGGGCTGGTCTCGAACTCCTGACCTGAAGTGATC T C RFX1 Ensembl:ENSG00000132005 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs932667808 Functional Loss SNV dbSNP153 33..33 33 - - - 24795 RMVar_ID_24795 Human_SNP_ID_659203641 A-to-I Human chr19 - 14001573 14001573 14001573 AATCCAGCCAGACTCAGTGGCTTATGCTTGTAATCCCAGCACTTCGGGAGGCTGAGACATGAGGA AATCCAGCCAGACTCAGTGGCTTATGCTTGTAGTCCCAGCACTTCGGGAGGCTGAGACATGAGGA T C RFX1 Ensembl:ENSG00000132005 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1203433187 Functional Loss SNV dbSNP153 33..33 33 - - - 24796 RMVar_ID_24796 Human_SNP_ID_659204075 A-to-I Human chr19 - 14003137 14003137 14003137 TACTAAAAATACAAAAAGTAGCCGGGCATGGTAGCACATGACTGTAGTAGTCCCAGCTATTTAGG TACTAAAAATACAAAAAGTAGCCGGGCATGGTGGCACATGACTGTAGTAGTCCCAGCTATTTAGG T C RFX1 Ensembl:ENSG00000132005 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256838023 Functional Loss SNV dbSNP153 33..33 33 - - - 24797 RMVar_ID_24797 Human_SNP_ID_659204089 A-to-I Human chr19 - 14003174 14003174 14003174 GGAGACCAGCCTGGCCAACACGGTGAAACCCTATCTCTACTAAAAATACAAAAAGTAGCCGGGCA GGAGACCAGCCTGGCCAACACGGTGAAACCCTGTCTCTACTAAAAATACAAAAAGTAGCCGGGCA T C RFX1 Ensembl:ENSG00000132005 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1192737271 Functional Loss SNV dbSNP153 33..33 33 - - - 24798 RMVar_ID_24798 Human_SNP_ID_659213758 A-to-I Human chr19 + 14036215 14036215 14036215 CAGAGTCTTGCTCTGTTGCCTAGGGTAGTCTCAAACTCCTGAGCTCAAGCGATCCTCCCATCTTG CAGAGTCTTGCTCTGTTGCCTAGGGTAGTCTCGAACTCCTGAGCTCAAGCGATCCTCCCATCTTG A G IL27RA Ensembl:ENSG00000104998 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1473472179 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97630,RMVar_hsa_circ_192959 24799 RMVar_ID_24799 Human_SNP_ID_659214375 A-to-I Human chr19 + 14038272 14038272 14038272 TCAATCGATCCTCCCACCCCAGCCTCTCAAGTAGTTGGAACCACAAGTGCGCGCCACTACCCCTG TCAATCGATCCTCCCACCCCAGCCTCTCAAGTGGTTGGAACCACAAGTGCGCGCCACTACCCCTG A G IL27RA Ensembl:ENSG00000104998 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1043565105 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97630,RMVar_hsa_circ_192959 24800 RMVar_ID_24800 Human_SNP_ID_659223959 A-to-I Human chr19 + 14070488 14070488 14070488 ACGCAGAAAGGAGATTCTATCAGCAGATGAACAGGCCTGTGGCAGGTGCCTCCCGCCAGGAGAAC ACGCAGAAAGGAGATTCTATCAGCAGATGAACGGGCCTGTGGCAGGTGCCTCCCGCCAGGAGAAC A G EEF1DP1 Ensembl:ENSG00000228887 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878874371 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1820640,Human_miRNA_ID_1862179 24801 RMVar_ID_24801 Human_SNP_ID_659223978 A-to-I Human chr19 + 14070540 14070540 14070540 CCGCCAGGAGAACGGCGCCAGCGTGATCCTCCATGACATTGTGAGAGCCAGAGAGAACATCCAGA CCGCCAGGAGAACGGCGCCAGCGTGATCCTCCGTGACATTGTGAGAGCCAGAGAGAACATCCAGA A G EEF1DP1 Ensembl:ENSG00000228887 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879252059 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6796980 Human_miRNA_ID_1829726 24802 RMVar_ID_24802 Human_SNP_ID_659231937 A-to-I Human chr19 - 14092758 14092758 14092758 CCAGGTCTTGCTGGTGTATCCAGGGACAGGGTATGGAAAGAGGGGCTCACGCTTAACTCCAGCCC CCAGGTCTTGCTGGTGTATCCAGGGACAGGGTGTGGAAAGAGGGGCTCACGCTTAACTCCAGCCC T C PRKACA Ensembl:ENSG00000072062 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1286461406 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_514056,Human_RBP_ID_6722205,Human_RBP_ID_8197591,Human_RBP_ID_17266777,Human_RBP_ID_17382176,Human_RBP_ID_17568477,Human_RBP_ID_18723135 Human_Splice_Rec_1968006 24803 RMVar_ID_24803 Human_SNP_ID_659234084 A-to-I Human chr19 - 14099564 14099563 14099564 AAAAAAAGTCAGGTGTGGTGGCACATTCCTGTAGTCCCAGCTCCTGGGGAGGCTGAGGTGGGAAG AAAAAAAGTCAGGTGTGGTGGCACATTCCTGT_GTCCCAGCTCCTGGGGAGGCTGAGGTGGGAAG CT C PRKACA Ensembl:ENSG00000072062 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1384511028 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_26483,RMVar_hsa_circ_321631,RMVar_hsa_circ_350951,RMVar_hsa_circ_192971 24804 RMVar_ID_24804 Human_SNP_ID_659239533 A-to-I Human chr19 - 14120302 14120302 14120302 CCCTAGGAAAGAACAGGCCTTGGGTCTCCCCTAGTCCTGGCCAGAAGGATGATCTCGCTTTTCCT CCCTAGGAAAGAACAGGCCTTGGGTCTCCCCTGGTCCTGGCCAGAAGGATGATCTCGCTTTTCCT T C ASF1B Ensembl:ENSG00000105011 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs559024702 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_514111,Human_RBP_ID_1013279,Human_RBP_ID_1187473,Human_RBP_ID_4504876,Human_RBP_ID_17266792,Human_RBP_ID_17382190,Human_RBP_ID_18723176,Human_RBP_ID_26465041 RMVar_hsa_circ_92962,RMVar_hsa_circ_112658,RMVar_hsa_circ_95845,RMVar_hsa_circ_192976,RMVar_hsa_circ_192977,RMVar_hsa_circ_192975 24805 RMVar_ID_24805 Human_SNP_ID_659242019 A-to-I Human chr19 - 14129426 14129426 14129426 GCAATCTGCCTGCCTCGGCCTCCCAAAGTGCTAGGATTACAGGTGTGAGCTGCCGTGCCCAACCA GCAATCTGCCTGCCTCGGCCTCCCAAAGTGCTTGGATTACAGGTGTGAGCTGCCGTGCCCAACCA T A ASF1B Ensembl:ENSG00000105011 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs948079572 Functional Loss SNV dbSNP153 33..33 33 - - - 24806 RMVar_ID_24806 Human_SNP_ID_659242160 A-to-I Human chr19 - 14129812 14129812 14129812 GAACTTCTGAGCTCAAGCAATCCACCCGCCTCAGCCTCCCAAAGTGCTAGGATTACAGCCATGAT GAACTTCTGAGCTCAAGCAATCCACCCGCCTCGGCCTCCCAAAGTGCTAGGATTACAGCCATGAT T C ASF1B Ensembl:ENSG00000105011 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1184552035 Functional Loss SNV dbSNP153 33..33 33 - - - 24807 RMVar_ID_24807 Human_SNP_ID_659242203 A-to-I Human chr19 - 14129953 14129953 14129953 TCACCCAGGCTGGAGTGCAGAGGCACGATCTCAGTTCACTGCAACCTCAGCCTCCCGAGTAGCTG TCACCCAGGCTGGAGTGCAGAGGCACGATCTCGGTTCACTGCAACCTCAGCCTCCCGAGTAGCTG T C ASF1B Ensembl:ENSG00000105011 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs916059276 Functional Loss SNV dbSNP153 33..33 33 - - - 24808 RMVar_ID_24808 Human_SNP_ID_659242207 A-to-I Human chr19 - 14129961 14129961 14129961 TCACTCTGTCACCCAGGCTGGAGTGCAGAGGCACGATCTCAGTTCACTGCAACCTCAGCCTCCCG TCACTCTGTCACCCAGGCTGGAGTGCAGAGGCGCGATCTCAGTTCACTGCAACCTCAGCCTCCCG T C ASF1B Ensembl:ENSG00000105011 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1315725104 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25385607 24809 RMVar_ID_24809 Human_SNP_ID_659242337 A-to-I Human chr19 - 14130486 14130486 14130486 TTTTTTTTTTTTTAAAGAGATAGGGTGTCACTATGTTGCCCAGACTGGACTTGAACTCCTGGGCT TTTTTTTTTTTTTAAAGAGATAGGGTGTCACTGTGTTGCCCAGACTGGACTTGAACTCCTGGGCT T C ASF1B Ensembl:ENSG00000105011 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973625134 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5131067,Human_RBP_ID_22476527 24810 RMVar_ID_24810 Human_SNP_ID_659242641 A-to-I Human chr19 - 14131325 14131325 14131325 CAAAAATTAGCCAGGCATGGTGGCACGCAGCTATAATCCCAGCTACTCAGGAGGCTGAGGCAGAA CAAAAATTAGCCAGGCATGGTGGCACGCAGCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGAA T C ASF1B Ensembl:ENSG00000105011 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1484727795 Functional Loss SNV dbSNP153 33..33 33 - - - 24811 RMVar_ID_24811 Human_SNP_ID_659243013 A-to-I Human chr19 - 14132718 14132718 14132718 CACCTCTCGAGTTCAAGCGATTCTCCGGCCTCAGTATCCCAAGTAGTTGGGATTACAAGCTTGAG CACCTCTCGAGTTCAAGCGATTCTCCGGCCTCGGTATCCCAAGTAGTTGGGATTACAAGCTTGAG T C ASF1B Ensembl:ENSG00000105011 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006724054 Functional Loss SNV dbSNP153 33..33 33 - - - 24812 RMVar_ID_24812 Human_SNP_ID_659243478 A-to-I Human chr19 - 14134085 14134085 14134085 TTAAAAATGGTTGTGGCCGAGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAG TTAAAAATGGTTGTGGCCGAGCGCGGTGGCTCTCGCCTGTAATCCCAGCACTTTGGGAGGCCGAG T A ASF1B Ensembl:ENSG00000105011 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1452270909 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_139592 24813 RMVar_ID_24813 Human_SNP_ID_659243740 A-to-I Human chr19 - 14135041 14135041 14135041 TTTAGTATTTTTAGTGGAGGCAGCGTTTCACCATGTTAGCCAGGTTGGTCTCGAACTCCTGACCT TTTAGTATTTTTAGTGGAGGCAGCGTTTCACCGTGTTAGCCAGGTTGGTCTCGAACTCCTGACCT T C ASF1B Ensembl:ENSG00000105011 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1423064792 Functional Loss SNV dbSNP153 33..33 33 - - - 24814 RMVar_ID_24814 Human_SNP_ID_659244797 A-to-I Human chr19 + 14138266 14138266 14138266 TACAAAAAATAAAAGAATAAGCCAGGTGTGGTAGTGCATACCTGTAGTGTCTGCTACTCCTGAAG TACAAAAAATAAAAGAATAAGCCAGGTGTGGTGGTGCATACCTGTAGTGTCTGCTACTCCTGAAG A G AC022098.1 Ensembl:ENSG00000267169 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1258447432 Functional Loss SNV dbSNP153 33..33 33 - - - 24815 RMVar_ID_24815 Human_SNP_ID_659249159 A-to-I Human chr19 - 14153911 14153911 14153911 TTTGAGACAGAGTCTCGTTCTGTCCCCAGGCTAGAGTGCAATGGCGCGATCTCGGCTCACTGCAA TTTGAGACAGAGTCTCGTTCTGTCCCCAGGCTGGAGTGCAATGGCGCGATCTCGGCTCACTGCAA T C ADGRL1 Ensembl:ENSG00000072071 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1464963260 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105291,RMVar_hsa_circ_116538,RMVar_hsa_circ_124913,RMVar_hsa_circ_120948,RMVar_hsa_circ_123869,RMVar_hsa_circ_117388,RMVar_hsa_circ_113827,RMVar_hsa_circ_115666,RMVar_hsa_circ_110229,RMVar_hsa_circ_192979,RMVar_hsa_circ_192983,RMVar_hsa_circ_192987,RMVar_hsa_circ_79878,RMVar_hsa_circ_192988,RMVar_hsa_circ_192985,RMVar_hsa_circ_192986,RMVar_hsa_circ_192984,RMVar_hsa_circ_192981,RMVar_hsa_circ_192982,RMVar_hsa_circ_192980 24816 RMVar_ID_24816 Human_SNP_ID_659255230 A-to-I Human chr19 - 14173203 14173203 14173203 TAATCCCAGCACTTTGGGAGGTCGAGACGGGTAGATTGTTTGAACCCAGGAGTTTGAGACCAGCC TAATCCCAGCACTTTGGGAGGTCGAGACGGGTGGATTGTTTGAACCCAGGAGTTTGAGACCAGCC T C ADGRL1 Ensembl:ENSG00000072071 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs563094579 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120948,RMVar_hsa_circ_110229,RMVar_hsa_circ_192979,RMVar_hsa_circ_192980,RMVar_hsa_circ_34163 24817 RMVar_ID_24817 Human_SNP_ID_659260224 A-to-I Human chr19 + 14190031 14190031 14190031 GCTCACTGCAACTTCTCCCTCCCAGTTCAAGCAATTCTCGTGCCTCAGCCTCCTAAGTGGCCGGG GCTCACTGCAACTTCTCCCTCCCAGTTCAAGCTATTCTCGTGCCTCAGCCTCCTAAGTGGCCGGG A T lnc-MISP3-5,lnc-MISP3-5:2,lnc-MISP3-5:3 RNACentral:URS00008B30C6,RNACentral:URS00009B01DA,RNACentral:URS00009BC08F lincRNA,lincRNA,lincRNA exon,intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs944629541 Functional Loss SNV dbSNP153 33..33 33 - - - 24818 RMVar_ID_24818 Human_SNP_ID_659260975 A-to-I Human chr19 + 14192753 14192753 14192753 TCGTATTTTTAGTAGAGACGGGGTTTCGCCATATTGGTCAGGCTGCTCTCGAACTCCCAACCTCA TCGTATTTTTAGTAGAGACGGGGTTTCGCCATGTTGGTCAGGCTGCTCTCGAACTCCCAACCTCA A G lnc-MISP3-5,lnc-MISP3-5:2 RNACentral:URS00008B30C6,RNACentral:URS00009B01DA lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1034522941 Functional Loss SNV dbSNP153 33..33 33 - - - 24819 RMVar_ID_24819 Human_SNP_ID_659260976 A-to-I Human chr19 + 14192753 14192753 14192753 TCGTATTTTTAGTAGAGACGGGGTTTCGCCATATTGGTCAGGCTGCTCTCGAACTCCCAACCTCA TCGTATTTTTAGTAGAGACGGGGTTTCGCCATTTTGGTCAGGCTGCTCTCGAACTCCCAACCTCA A T lnc-MISP3-5,lnc-MISP3-5:2 RNACentral:URS00008B30C6,RNACentral:URS00009B01DA lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1034522941 Functional Loss SNV dbSNP153 33..33 33 - - - 24820 RMVar_ID_24820 Human_SNP_ID_659261928 A-to-I Human chr19 - 14196446 14196446 14196446 CTGGCTAACTTTTTGTATTTTTGGCAGAGACAAGGTTTCACTATGTTCCCCAGGCTGGTCTGGAA CTGGCTAACTTTTTGTATTTTTGGCAGAGACAGGGTTTCACTATGTTCCCCAGGCTGGTCTGGAA T C ADGRL1 Ensembl:ENSG00000072071 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956722389 Functional Loss SNV dbSNP153 33..33 33 - - - 24821 RMVar_ID_24821 Human_SNP_ID_659292646 A-to-I Human chr19 - 14305414 14305414 14305414 GAAACCCCATCTCTACTAAAAATACAAAAATTAGCTGGGTGTGGTGGTGCACCTACAGGCCCAGC GAAACCCCATCTCTACTAAAAATACAAAAATTGGCTGGGTGTGGTGGTGCACCTACAGGCCCAGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1203083093 Functional Loss SNV dbSNP153 33..33 33 - - - 24822 RMVar_ID_24822 Human_SNP_ID_659316199 A-to-I Human chr19 + 14390507 14390506 14390508 CACCATGCCCAGATAATTTTTGTATTTTTAGTAGAGACGGGGTTTTGCCATCTTGGCCAGGCTGG CACCATGCCCAGATAATTTTTGTATTTTTAGT__AGACGGGGTTTTGCCATCTTGGCCAGGCTGG TAG T ADGRE5 Ensembl:ENSG00000123146 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs919238143 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_81043,RMVar_hsa_circ_19864,RMVar_hsa_circ_192998,RMVar_hsa_circ_25743 24823 RMVar_ID_24823 Human_SNP_ID_659318514 A-to-I Human chr19 + 14398396 14398396 14398396 CAGCACTTAAGAACCTGGAGTTGAGGCCGGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTG CAGCACTTAAGAACCTGGAGTTGAGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTG A G ADGRE5 Ensembl:ENSG00000123146 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs949886227 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3051,RMVar_hsa_circ_81043,RMVar_hsa_circ_19864,RMVar_hsa_circ_192998,RMVar_hsa_circ_368847,RMVar_hsa_circ_19498 24824 RMVar_ID_24824 Human_SNP_ID_659319331 A-to-I Human chr19 + 14401077 14401077 14401077 GTCTGGGAGGTGGAGGTTGCAGTGAGCTGATTATGCCACTGCACTCAAGCCTGGGCAACAGACTG GTCTGGGAGGTGGAGGTTGCAGTGAGCTGATTGTGCCACTGCACTCAAGCCTGGGCAACAGACTG A G ADGRE5 Ensembl:ENSG00000123146 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1320708735 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3051,RMVar_hsa_circ_81043,RMVar_hsa_circ_19864,RMVar_hsa_circ_192998,RMVar_hsa_circ_368847,RMVar_hsa_circ_19498 24825 RMVar_ID_24825 Human_SNP_ID_659319989 A-to-I Human chr19 + 14403222 14403222 14403222 GCGCCACCACACCTCGCTGATTTTGTATTTTTAGTAGAGACGGGGTTTCTCCATGTTGGTCAGGT GCGCCACCACACCTCGCTGATTTTGTATTTTTGGTAGAGACGGGGTTTCTCCATGTTGGTCAGGT A G ADGRE5 Ensembl:ENSG00000123146 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1209695252 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3051,RMVar_hsa_circ_81043,RMVar_hsa_circ_19864,RMVar_hsa_circ_192998,RMVar_hsa_circ_19498,RMVar_hsa_circ_192999,RMVar_hsa_circ_352637,RMVar_hsa_circ_125690,RMVar_hsa_circ_281569,RMVar_hsa_circ_193000,RMVar_hsa_circ_193001 24826 RMVar_ID_24826 Human_SNP_ID_659322704 A-to-I Human chr19 - 14411006 14411006 14411006 TGTGAAGCACTTTGTGCTGGACGAGTGTGACAAGATGCTGGAGCAGCTGGGTGAGTCCTCTGCCC TGTGAAGCACTTTGTGCTGGACGAGTGTGACAGGATGCTGGAGCAGCTGGGTGAGTCCTCTGCCC T C DDX39A Ensembl:ENSG00000123136 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs745797080 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_280123,Human_RBP_ID_907427,Human_RBP_ID_1555556,Human_RBP_ID_1880534,Human_RBP_ID_3563676,Human_RBP_ID_3954598,Human_RBP_ID_5585409,Human_RBP_ID_8478220,Human_RBP_ID_9380664,Human_RBP_ID_18994473,Human_RBP_ID_23783906,Human_RBP_ID_26983922 Human_Splice_Rec_1968447,Human_Splice_Rec_1968473,Human_Splice_Rec_1968491,Human_Splice_Rec_1968505,Human_Splice_Rec_1968519,Human_Splice_Rec_1968529,Human_Splice_Rec_1968543,Human_Splice_Rec_1968555,Human_Splice_Rec_1968567,Human_Splice_Rec_1968569,Human_Splice_Rec_1968579 Human_miRNA_ID_2442359 RMVar_hsa_circ_3830,RMVar_hsa_circ_70824,RMVar_hsa_circ_14736,RMVar_hsa_circ_193006,RMVar_hsa_circ_372402,RMVar_hsa_circ_126570,RMVar_hsa_circ_193007 24827 RMVar_ID_24827 Human_SNP_ID_659323376 A-to-I Human chr19 - 14413176 14413176 14413176 GATGTGGAAAACGATCTTTTGGATTACGATGAAGAGGAAGAGCCCCAGGCTCCTCAAGAGAGCAC GATGTGGAAAACGATCTTTTGGATTACGATGAGGAGGAAGAGCCCCAGGCTCCTCAAGAGAGCAC T C DDX39A Ensembl:ENSG00000123136 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs112820981 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_55198,Human_RBP_ID_908493,Human_RBP_ID_1555566,Human_RBP_ID_1880541,Human_RBP_ID_3563679,Human_RBP_ID_13377251,Human_RBP_ID_18412303,Human_RBP_ID_18544488,Human_RBP_ID_22967317,Human_RBP_ID_26983939,Human_RBP_ID_27816197 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 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 24828 RMVar_ID_24828 Human_SNP_ID_659323785 A-to-I Human chr19 - 14414519 14414519 14414519 TGGTGAAACCCTGTCTCTACGAAAACTACAAAAATTAGCTGGGCATGGTGGCAAGCACCTGTAAT TGGTGAAACCCTGTCTCTACGAAAACTACAAACATTAGCTGGGCATGGTGGCAAGCACCTGTAAT T G DDX39A Ensembl:ENSG00000123136 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170268836 Functional Loss SNV dbSNP153 33..33 33 - - - 24829 RMVar_ID_24829 Human_SNP_ID_659323844 A-to-I Human chr19 - 14414738 14414738 14414738 GCTGGTCTCGAACTCCTGACTTCAGGTGACCCACCCGCCTTGGTCTCTCAAAAGTGCTGGGATTA GCTGGTCTCGAACTCCTGACTTCAGGTGACCCGCCCGCCTTGGTCTCTCAAAAGTGCTGGGATTA T C DDX39A Ensembl:ENSG00000123136 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1479714971 Functional Loss SNV dbSNP153 33..33 33 - - - 24830 RMVar_ID_24830 Human_SNP_ID_659323868 A-to-I Human chr19 - 14414853 14414853 14414853 TTAAGCAATTTTTCTGCCTCAGCTTCCCGAGTAGCTGGGATTATAGGCGCCTGCCACCATGCCTG TTAAGCAATTTTTCTGCCTCAGCTTCCCGAGTTGCTGGGATTATAGGCGCCTGCCACCATGCCTG T A DDX39A Ensembl:ENSG00000123136 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1488104662 Functional Loss SNV dbSNP153 33..33 33 - - - 24831 RMVar_ID_24831 Human_SNP_ID_659323873 A-to-I Human chr19 - 14414865 14414865 14414865 CGCCTCCCAGGTTTAAGCAATTTTTCTGCCTCAGCTTCCCGAGTAGCTGGGATTATAGGCGCCTG CGCCTCCCAGGTTTAAGCAATTTTTCTGCCTCCGCTTCCCGAGTAGCTGGGATTATAGGCGCCTG T G DDX39A Ensembl:ENSG00000123136 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1468769483 Functional Loss SNV dbSNP153 33..33 33 - - - 24832 RMVar_ID_24832 Human_SNP_ID_659324054 A-to-I Human chr19 - 14415432 14415432 14415432 ATTAGTGGTGGCGGGCGCATGTAGCTCCTGCTACTAGGGAGGCTGAGGTGGGAAGATCGCTTGAT ATTAGTGGTGGCGGGCGCATGTAGCTCCTGCTTCTAGGGAGGCTGAGGTGGGAAGATCGCTTGAT T A DDX39A Ensembl:ENSG00000123136 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1436079813 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25386149 24833 RMVar_ID_24833 Human_SNP_ID_659324091 A-to-I Human chr19 - 14415564 14415564 14415564 GGCCAGGTGTGGTGGCTCACACCTGTAATCCCAGCACTTTGGAAGGCTGAGGTGGGCGGATCGCC GGCCAGGTGTGGTGGCTCACACCTGTAATCCCCGCACTTTGGAAGGCTGAGGTGGGCGGATCGCC T G DDX39A Ensembl:ENSG00000123136 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1055113776 Functional Loss SNV dbSNP153 33..33 33 - - - 24834 RMVar_ID_24834 Human_SNP_ID_659324181 A-to-I Human chr19 - 14415909 14415909 14415909 GCCACCACACCCGGCACATTTTTGGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGTCAGGC GCCACCACACCCGGCACATTTTTGGTATTTTTGGTAGAGATGGGGTTTCACCATGTTGGTCAGGC T C DDX39A Ensembl:ENSG00000123136 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1007282442 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1968602 24835 RMVar_ID_24835 Human_SNP_ID_659324397 A-to-I Human chr19 - 14416853 14416853 14416853 CGTGGTGAAACACTGTCTCTACTAAAACAAAAATTAGCCAGGCGTGGTGGCATGCACCTGTAGTC CGTGGTGAAACACTGTCTCTACTAAAACAAAACTTAGCCAGGCGTGGTGGCATGCACCTGTAGTC T G DDX39A Ensembl:ENSG00000123136 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs994703230 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9930086,Human_RBP_ID_22967327,Human_RBP_ID_25386167 24836 RMVar_ID_24836 Human_SNP_ID_659324425 A-to-I Human chr19 - 14416955 14416955 14416955 AGGCTGGGCGTGGTGGGTGGCTCATTCCTGTAATCCCAGCACTTTGGGAGGCAGAGGCAGGAGGT AGGCTGGGCGTGGTGGGTGGCTCATTCCTGTACTCCCAGCACTTTGGGAGGCAGAGGCAGGAGGT T G DDX39A Ensembl:ENSG00000123136 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1396324892 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13377322 24837 RMVar_ID_24837 Human_SNP_ID_659324698 A-to-I Human chr19 - 14418006 14418006 14418006 AGCAAGCACATCCGGCTAATTTTTGTATTTGTAGTAGAGACGGGGTTTCACCATGTTGCCCAGGC AGCAAGCACATCCGGCTAATTTTTGTATTTGTGGTAGAGACGGGGTTTCACCATGTTGCCCAGGC T C DDX39A Ensembl:ENSG00000123136 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1413695161 Functional Loss SNV dbSNP153 33..33 33 - - - 24838 RMVar_ID_24838 Human_SNP_ID_659335789 A-to-I Human chr19 + 14457211 14457211 14457211 AGGCCTGGTGGCTCATGCCTGTAATCCCAGATACTTGGGAGGCTGAGGCAGGAGAATATCACTTG AGGCCTGGTGGCTCATGCCTGTAATCCCAGATGCTTGGGAGGCTGAGGCAGGAGAATATCACTTG A G PKN1 Ensembl:ENSG00000123143 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs913233768 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81540,RMVar_hsa_circ_124635,RMVar_hsa_circ_193010,RMVar_hsa_circ_193012,RMVar_hsa_circ_23126 24839 RMVar_ID_24839 Human_SNP_ID_659338078 A-to-I Human chr19 + 14464730 14464730 14464730 ATCAGTTGAACCTGAGAGGCGGAGGTTGCAGTAAGCCAAGATCATACCAATTGCGCTCCAGCCTG ATCAGTTGAACCTGAGAGGCGGAGGTTGCAGTGAGCCAAGATCATACCAATTGCGCTCCAGCCTG A G PKN1 Ensembl:ENSG00000123143 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1480453622 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22967335,Human_RBP_ID_25386248 RMVar_hsa_circ_81540,RMVar_hsa_circ_124635,RMVar_hsa_circ_193010,RMVar_hsa_circ_77320,RMVar_hsa_circ_193012,RMVar_hsa_circ_23126,RMVar_hsa_circ_8816,RMVar_hsa_circ_105484,RMVar_hsa_circ_193017,RMVar_hsa_circ_193018 24840 RMVar_ID_24840 Human_SNP_ID_659344032 A-to-I Human chr19 - 14481398 14481398 14481398 TTTTTGCTAGGACCGAAATCCTAGCTGGGTACAGTGGTGCACACCTATAGTCCCAGCTACTTGGG TTTTTGCTAGGACCGAAATCCTAGCTGGGTACGGTGGTGCACACCTATAGTCCCAGCTACTTGGG T C GIPC1 Ensembl:ENSG00000123159 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1469469086 Functional Loss SNV dbSNP153 33..33 33 - - - 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 24841 RMVar_ID_24841 Human_SNP_ID_659344990 A-to-I Human chr19 - 14484247 14484247 14484247 CATGTAATCCCAGCTTCTTGGGAGGCTGAGACAAGAGAATCGCTTGTACCCGGGAGGCAAGAGAT CATGTAATCCCAGCTTCTTGGGAGGCTGAGACGAGAGAATCGCTTGTACCCGGGAGGCAAGAGAT T C GIPC1 Ensembl:ENSG00000123159 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1369321583 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25386287 RMVar_hsa_circ_80215,RMVar_hsa_circ_193026,RMVar_hsa_circ_88431,RMVar_hsa_circ_193028 24842 RMVar_ID_24842 Human_SNP_ID_659345002 A-to-I Human chr19 - 14484303 14484303 14484303 GGTGAAACCCCATCTCTACCAAAAATGTAGAAATTACCCCGGTGTGGTGGCACAGACATGTAATC GGTGAAACCCCATCTCTACCAAAAATGTAGAAGTTACCCCGGTGTGGTGGCACAGACATGTAATC T C GIPC1 Ensembl:ENSG00000123159 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs932420498 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80215,RMVar_hsa_circ_193026,RMVar_hsa_circ_88431,RMVar_hsa_circ_193028 24843 RMVar_ID_24843 Human_SNP_ID_659346297 A-to-I Human chr19 - 14488215 14488215 14488215 AACTGCTGACCTCATGTGATCCGTCAACCTCAACCTCCCAAAGTGCTGGGATTACAGGCTTGAGC AACTGCTGACCTCATGTGATCCGTCAACCTCAGCCTCCCAAAGTGCTGGGATTACAGGCTTGAGC T C GIPC1 Ensembl:ENSG00000123159 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404714380 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80215,RMVar_hsa_circ_193026,RMVar_hsa_circ_88431,RMVar_hsa_circ_193028 24844 RMVar_ID_24844 Human_SNP_ID_659346299 A-to-I Human chr19 - 14488221 14488221 14488221 GTCTCAAACTGCTGACCTCATGTGATCCGTCAACCTCAACCTCCCAAAGTGCTGGGATTACAGGC GTCTCAAACTGCTGACCTCATGTGATCCGTCATCCTCAACCTCCCAAAGTGCTGGGATTACAGGC T A GIPC1 Ensembl:ENSG00000123159 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs545804870 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80215,RMVar_hsa_circ_193026,RMVar_hsa_circ_88431,RMVar_hsa_circ_193028 24845 RMVar_ID_24845 Human_SNP_ID_659346300 A-to-I Human chr19 - 14488221 14488221 14488221 GTCTCAAACTGCTGACCTCATGTGATCCGTCAACCTCAACCTCCCAAAGTGCTGGGATTACAGGC GTCTCAAACTGCTGACCTCATGTGATCCGTCAGCCTCAACCTCCCAAAGTGCTGGGATTACAGGC T C GIPC1 Ensembl:ENSG00000123159 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs545804870 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80215,RMVar_hsa_circ_193026,RMVar_hsa_circ_88431,RMVar_hsa_circ_193028 24846 RMVar_ID_24846 Human_SNP_ID_659346301 A-to-I Human chr19 - 14488221 14488221 14488221 GTCTCAAACTGCTGACCTCATGTGATCCGTCAACCTCAACCTCCCAAAGTGCTGGGATTACAGGC GTCTCAAACTGCTGACCTCATGTGATCCGTCACCCTCAACCTCCCAAAGTGCTGGGATTACAGGC T G GIPC1 Ensembl:ENSG00000123159 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs545804870 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80215,RMVar_hsa_circ_193026,RMVar_hsa_circ_88431,RMVar_hsa_circ_193028 24847 RMVar_ID_24847 Human_SNP_ID_659346396 A-to-I Human chr19 - 14488549 14488549 14488549 CGGGGTTTCACCATGTTGGTCAGGCTGGCCTCAAACTCCTGACCTCATGATCCGCCTGCCTTGGC CGGGGTTTCACCATGTTGGTCAGGCTGGCCTCGAACTCCTGACCTCATGATCCGCCTGCCTTGGC T C GIPC1 Ensembl:ENSG00000123159 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1356057988 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80215,RMVar_hsa_circ_193026,RMVar_hsa_circ_88431,RMVar_hsa_circ_193028 24848 RMVar_ID_24848 Human_SNP_ID_659346404 A-to-I Human chr19 - 14488569 14488569 14488569 TTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGTCAGGCTGGCCTCAAACTCCTGACCT TTTTGTATTTTTAGTAGAGACGGGGTTTCACCGTGTTGGTCAGGCTGGCCTCAAACTCCTGACCT T C GIPC1 Ensembl:ENSG00000123159 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1291366597 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80215,RMVar_hsa_circ_193026,RMVar_hsa_circ_88431,RMVar_hsa_circ_193028 24849 RMVar_ID_24849 Human_SNP_ID_659346412 A-to-I Human chr19 - 14488595 14488595 14488595 TGCATGCACCACCATACCTGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGG TGCATGCACCACCATACCTGGCTAATTTTTGTGTTTTTAGTAGAGACGGGGTTTCACCATGTTGG T C GIPC1 Ensembl:ENSG00000123159 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1426045563 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80215,RMVar_hsa_circ_193026,RMVar_hsa_circ_88431,RMVar_hsa_circ_193028 24850 RMVar_ID_24850 Human_SNP_ID_659346413 A-to-I Human chr19 - 14488603 14488603 14488603 ATGAGGTTTGCATGCACCACCATACCTGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCAC ATGAGGTTTGCATGCACCACCATACCTGGCTAGTTTTTGTATTTTTAGTAGAGACGGGGTTTCAC T C GIPC1 Ensembl:ENSG00000123159 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs541963259 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80215,RMVar_hsa_circ_193026,RMVar_hsa_circ_88431,RMVar_hsa_circ_193028 24851 RMVar_ID_24851 Human_SNP_ID_659346439 A-to-I Human chr19 - 14488721 14488721 14488721 TCGCCCAGGCTGGAGTGCAATGGCGTGATCTCAGCTCACTGCAACCTCAGCCTCAGGAGTAGCTG TCGCCCAGGCTGGAGTGCAATGGCGTGATCTCGGCTCACTGCAACCTCAGCCTCAGGAGTAGCTG T C GIPC1 Ensembl:ENSG00000123159 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs564230663 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23309297 RMVar_hsa_circ_80215,RMVar_hsa_circ_193026,RMVar_hsa_circ_88431,RMVar_hsa_circ_193028 24852 RMVar_ID_24852 Human_SNP_ID_659346531 A-to-I Human chr19 - 14489050 14489050 14489050 ATGGCTGTGAACACCTGTAGTCTCAGCTATTCAGGAGGTTGAGACAGGAGGATTGCTTGAGCCCA ATGGCTGTGAACACCTGTAGTCTCAGCTATTCGGGAGGTTGAGACAGGAGGATTGCTTGAGCCCA T C GIPC1 Ensembl:ENSG00000123159 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935218785 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9909362,Human_RBP_ID_13377541 RMVar_hsa_circ_80215,RMVar_hsa_circ_193026,RMVar_hsa_circ_88431,RMVar_hsa_circ_193028 24853 RMVar_ID_24853 Human_SNP_ID_659346551 A-to-I Human chr19 - 14489122 14489122 14489122 GCCCAGGAGTTCAGGACCAATCTGGGCAACGTAGTGAGACCCGTCTCTACAAAAAATAAAAATTA GCCCAGGAGTTCAGGACCAATCTGGGCAACGTGGTGAGACCCGTCTCTACAAAAAATAAAAATTA T C GIPC1 Ensembl:ENSG00000123159 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223211248 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80215,RMVar_hsa_circ_193026,RMVar_hsa_circ_88431,RMVar_hsa_circ_193028 24854 RMVar_ID_24854 Human_SNP_ID_659346560 A-to-I Human chr19 - 14489142 14489142 14489142 AAGGCGGGAGGATTGCTTGAGCCCAGGAGTTCAGGACCAATCTGGGCAACGTAGTGAGACCCGTC AAGGCGGGAGGATTGCTTGAGCCCAGGAGTTCGGGACCAATCTGGGCAACGTAGTGAGACCCGTC T C GIPC1 Ensembl:ENSG00000123159 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1402603954 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25386330 RMVar_hsa_circ_80215,RMVar_hsa_circ_193026,RMVar_hsa_circ_88431,RMVar_hsa_circ_193028 24855 RMVar_ID_24855 Human_SNP_ID_659346568 A-to-I Human chr19 - 14489195 14489195 14489195 TAGCAGGCTGGGTGTGGTAGCTCATGCCTATAATCCCAGCACTTTGGAAGGCCAAGGCGGGAGGA TAGCAGGCTGGGTGTGGTAGCTCATGCCTATATTCCCAGCACTTTGGAAGGCCAAGGCGGGAGGA T A GIPC1 Ensembl:ENSG00000123159 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs952347085 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80215,RMVar_hsa_circ_193026,RMVar_hsa_circ_88431,RMVar_hsa_circ_193028 24856 RMVar_ID_24856 Human_SNP_ID_659347065 A-to-I Human chr19 - 14490594 14490594 14490594 CAGCTCACCTCAACCTCTGCCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCTAGTAGCT CAGCTCACCTCAACCTCTGCCTCCCAGGTTCACGCGATTCTCCTGCCTCAGCCTCCCTAGTAGCT T G GIPC1 Ensembl:ENSG00000123159 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1219746462 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80215,RMVar_hsa_circ_193026,RMVar_hsa_circ_88431,RMVar_hsa_circ_193028 24857 RMVar_ID_24857 Human_SNP_ID_659347068 A-to-I Human chr19 - 14490601 14490601 14490601 ACTGTCTCAGCTCACCTCAACCTCTGCCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCT ACTGTCTCAGCTCACCTCAACCTCTGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCT T C GIPC1 Ensembl:ENSG00000123159 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1200304193 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80215,RMVar_hsa_circ_193026,RMVar_hsa_circ_88431,RMVar_hsa_circ_193028 24858 RMVar_ID_24858 Human_SNP_ID_659356807 A-to-I Human chr19 - 14520898 14520898 14520898 GCCTCAAATTCCTGGGCTCAAGCTATCCTCCTACCTTGGTCCACTGAGTAGCTGGGACTACAGGC GCCTCAAATTCCTGGGCTCAAGCTATCCTCCTGCCTTGGTCCACTGAGTAGCTGGGACTACAGGC T C DNAJB1 Ensembl:ENSG00000132002 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs548183114 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95237,RMVar_hsa_circ_88931,RMVar_hsa_circ_193032,RMVar_hsa_circ_193033 24859 RMVar_ID_24859 Human_SNP_ID_659361668 A-to-I Human chr19 + 14537845 14537845 14537845 CTCGGCTCGCTGCACCTCCGCCTCCCGGGTTCAGGCGATTCTCCTGCCTTAGTCTCCCGAGTAGC CTCGGCTCGCTGCACCTCCGCCTCCCGGGTTCGGGCGATTCTCCTGCCTTAGTCTCCCGAGTAGC A G TECR Ensembl:ENSG00000099797 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1323756574 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83303,RMVar_hsa_circ_193034 24860 RMVar_ID_24860 Human_SNP_ID_659364432 A-to-I Human chr19 + 14546434 14546434 14546434 CATGCTGAAACCCCTCTTCTACTAAAAATACAAAAATTAACCAGGTGCAGTGGCACGTGTCTGTA CATGCTGAAACCCCTCTTCTACTAAAAATACAGAAATTAACCAGGTGCAGTGGCACGTGTCTGTA A G TECR Ensembl:ENSG00000099797 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1478145524 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112622,RMVar_hsa_circ_83303,RMVar_hsa_circ_193034,RMVar_hsa_circ_193035 24861 RMVar_ID_24861 Human_SNP_ID_659364434 A-to-I Human chr19 + 14546440 14546440 14546440 GAAACCCCTCTTCTACTAAAAATACAAAAATTAACCAGGTGCAGTGGCACGTGTCTGTAATCCTG GAAACCCCTCTTCTACTAAAAATACAAAAATTGACCAGGTGCAGTGGCACGTGTCTGTAATCCTG A G TECR Ensembl:ENSG00000099797 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1265399725 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112622,RMVar_hsa_circ_83303,RMVar_hsa_circ_193034,RMVar_hsa_circ_193035 24862 RMVar_ID_24862 Human_SNP_ID_659364567 A-to-I Human chr19 + 14546910 14546910 14546910 CAGGGTTTCACTATGTTGGCCAGGCTGGTCTCAAACTCCTGACCTCAAGTGATCTGATCTGCCCG CAGGGTTTCACTATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAAGTGATCTGATCTGCCCG A G TECR Ensembl:ENSG00000099797 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1442702402 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13378174 RMVar_hsa_circ_112622,RMVar_hsa_circ_83303,RMVar_hsa_circ_193034,RMVar_hsa_circ_193035 24863 RMVar_ID_24863 Human_SNP_ID_659365379 A-to-I Human chr19 + 14549667 14549667 14549667 GCTTTTGGCCTCTTTATAAAATACTGTAGGCCAGGCGCAGTGGCTCACGCCTGTAATCCCAGCAC GCTTTTGGCCTCTTTATAAAATACTGTAGGCCGGGCGCAGTGGCTCACGCCTGTAATCCCAGCAC A G TECR Ensembl:ENSG00000099797 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs981166787 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112622,RMVar_hsa_circ_83303,RMVar_hsa_circ_193034,RMVar_hsa_circ_193035 24864 RMVar_ID_24864 Human_SNP_ID_659371539 A-to-I Human chr19 - 14568277 14568277 14568277 ACTTTGGGAGGCCAAGGTGGGTGGATCACCTGAGGTCAGGAGTTCAAGACCAGCCTGACTAACAT ACTTTGGGAGGCCAAGGTGGGTGGATCACCTGCGGTCAGGAGTTCAAGACCAGCCTGACTAACAT T G NDUFB7 Ensembl:ENSG00000099795 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1225832331 Functional Loss SNV dbSNP153 33..33 33 - - - 24865 RMVar_ID_24865 Human_SNP_ID_659371557 A-to-I Human chr19 - 14568334 14568333 14568335 GCAGCAGAGAAAAAGGCTCTCAGGCCGGGCACAGTGGCTCACACCTGTAATCCCAGCACTTTGGG GCAGCAGAGAAAAAGGCTCTCAGGCCGGGCA__GTGGCTCACACCTGTAATCCCAGCACTTTGGG CTG C NDUFB7 Ensembl:ENSG00000099795 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1382955850 Functional Loss DEL dbSNP153 32..33 33 - - - 24866 RMVar_ID_24866 Human_SNP_ID_659371724 A-to-I Human chr19 - 14568958 14568958 14568958 GTTGGCCAGGCTGATCTCGAACTTCTGACCTCAAGTGATCCACCTGCCTCGGCCTCCCAAAGTGC GTTGGCCAGGCTGATCTCGAACTTCTGACCTCTAGTGATCCACCTGCCTCGGCCTCCCAAAGTGC T A NDUFB7 Ensembl:ENSG00000099795 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs906175155 Functional Loss SNV dbSNP153 33..33 33 - - - 24867 RMVar_ID_24867 Human_SNP_ID_659371744 A-to-I Human chr19 - 14569053 14569053 14569053 CTCCCGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGTGCGTGCCACCACACCTGACTCATTTTT CTCCCGCCTCAGCCTCCCGAGTAGCTGGGATTTCAGGTGCGTGCCACCACACCTGACTCATTTTT T A NDUFB7 Ensembl:ENSG00000099795 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs989872900 Functional Loss SNV dbSNP153 33..33 33 - - - 24868 RMVar_ID_24868 Human_SNP_ID_659371988 A-to-I Human chr19 - 14570030 14570030 14570030 AAAATTAGCCAGGTGTGGTGGCGCATGCCTGTAATCCCAGCTGTCTGGGAGGCTGAGGCAGGAGA AAAATTAGCCAGGTGTGGTGGCGCATGCCTGTTATCCCAGCTGTCTGGGAGGCTGAGGCAGGAGA T A NDUFB7 Ensembl:ENSG00000099795 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1371821698 Functional Loss SNV dbSNP153 33..33 33 - - - 24869 RMVar_ID_24869 Human_SNP_ID_659372062 A-to-I Human chr19 - 14570311 14570311 14570311 CCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACCCAGGAGGCAGAGGTT CCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCGGGAGAATCGCTTGAACCCAGGAGGCAGAGGTT T C NDUFB7 Ensembl:ENSG00000099795 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs946620024 Functional Loss SNV dbSNP153 33..33 33 - - - 24870 RMVar_ID_24870 Human_SNP_ID_659372376 A-to-I Human chr19 - 14571475 14571475 14571475 CTCCTGCCTCAGCCTCGCGAGTAGCTGTGATTACAGATGTGTACCACCATGCCCAGCTACTTTTT CTCCTGCCTCAGCCTCGCGAGTAGCTGTGATTGCAGATGTGTACCACCATGCCCAGCTACTTTTT T C NDUFB7 Ensembl:ENSG00000099795 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1275872996 Functional Loss SNV dbSNP153 33..33 33 - - - 24871 RMVar_ID_24871 Human_SNP_ID_659379507 A-to-I Human chr19 + 14596487 14596487 14596487 ACCCCCATCTCTGCAAAAAAATAAAATAAATTAGCTGGGCCTAGTGGCACACATCTATAGACCCA ACCCCCATCTCTGCAAAAAAATAAAATAAATTGGCTGGGCCTAGTGGCACACATCTATAGACCCA A G CLEC17A Ensembl:ENSG00000187912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs928163683 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_193055,RMVar_hsa_circ_375938,RMVar_hsa_circ_193056,RMVar_hsa_circ_373011 24872 RMVar_ID_24872 Human_SNP_ID_659379841 A-to-I Human chr19 + 14597718 14597718 14597718 CCATGATCACACTCAAGAGATCCTCCTGCCTCAGCCTCTTGAGTAGCTGGGACATAGGCGCATGC CCATGATCACACTCAAGAGATCCTCCTGCCTCCGCCTCTTGAGTAGCTGGGACATAGGCGCATGC A C CLEC17A Ensembl:ENSG00000187912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1490030153 Functional Loss SNV dbSNP153 33..33 33 - - - 24873 RMVar_ID_24873 Human_SNP_ID_659379906 A-to-I Human chr19 + 14597921 14597921 14597921 CCTGTGTTTCTGTTTTGTCCAACTGAAGGGCCAGCTACTGAGCTAGCGAGTGTTGAAAAAGGGAA CCTGTGTTTCTGTTTTGTCCAACTGAAGGGCCTGCTACTGAGCTAGCGAGTGTTGAAAAAGGGAA A T CLEC17A Ensembl:ENSG00000187912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1028738205 Functional Loss SNV dbSNP153 33..33 33 - - - 24874 RMVar_ID_24874 Human_SNP_ID_659383577 A-to-I Human chr19 + 14611730 14611730 14611730 TGATGATATAATTCACTTTACTTGCCAGGCACAGTGGCTCACGCCTGTAATCCCAGCACTCTGGG TGATGATATAATTCACTTTACTTGCCAGGCACCGTGGCTCACGCCTGTAATCCCAGCACTCTGGG A C CLEC17A Ensembl:ENSG00000187912 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1041288458 Functional Loss SNV dbSNP153 33..33 33 - - - 24875 RMVar_ID_24875 Human_SNP_ID_659383587 A-to-I Human chr19 + 14611792 14611792 14611792 GGGAGACTGAGGTGGGCTGATCACCTGGGGTCAGGATTTCGAGACCAGCCTGGCCAACATGGTAA GGGAGACTGAGGTGGGCTGATCACCTGGGGTCGGGATTTCGAGACCAGCCTGGCCAACATGGTAA A G CLEC17A Ensembl:ENSG00000187912 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs901140011 Functional Loss SNV dbSNP153 33..33 33 - - - 24876 RMVar_ID_24876 Human_SNP_ID_659408264 A-to-I Human chr19 + 14701306 14701306 14701306 TCACCTAGGCAGGAGTGCACTGGCACGATCATAGCTCCCTGTAGCTTTGAACTTATTAGCTCAAG TCACCTAGGCAGGAGTGCACTGGCACGATCATGGCTCCCTGTAGCTTTGAACTTATTAGCTCAAG A G ZNF333 Ensembl:ENSG00000160961 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1458587125 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87634,RMVar_hsa_circ_193059,RMVar_hsa_circ_320655,RMVar_hsa_circ_193061 24877 RMVar_ID_24877 Human_SNP_ID_659416334 A-to-I Human chr19 - 14734438 14734438 14734438 CTGCTCACTGCAGCCTCGACCTCCCAAGGCCTAAGCAATCCTCCTGCCTCAGTCCCCCTCCAGGT CTGCTCACTGCAGCCTCGACCTCCCAAGGCCTGAGCAATCCTCCTGCCTCAGTCCCCCTCCAGGT T C ADGRE2 Ensembl:ENSG00000127507 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1441266368 Functional Loss SNV dbSNP153 33..33 33 - - - 24878 RMVar_ID_24878 Human_SNP_ID_707335441 A-to-I Human chrX + 286274 286274 286274 TTTAGCAGAGATGGGGTTTCACCATGTTGGTCAAGCTGGTCTCGAACTCCCGACCTCAGGCAATC TTTAGCAGAGATGGGGTTTCACCATGTTGGTCGAGCTGGTCTCGAACTCCCGACCTCAGGCAATC A G PLCXD1 Ensembl:ENSG00000182378 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1290195927 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28257,RMVar_hsa_circ_289750,RMVar_hsa_circ_344677,RMVar_hsa_circ_273785,RMVar_hsa_circ_261159,RMVar_hsa_circ_261160 24879 RMVar_ID_24879 Human_SNP_ID_707341080 A-to-I Human chrX + 299593 299564 299593 CAGCCTGACCAACATGGTGAAATCCCATCTCTACTAAAAATACAAAACTTAGCTGGGTGTGTGGC CAGC_____________________________CTAAAAATACAAAACTTAGCTGGGTGTGTGGC CCTGACCAACATGGTGAAATCCCATCTCTA C PLCXD1 Ensembl:ENSG00000182378 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1170669139 Functional Loss DEL dbSNP153 5..33 33 - - - 24880 RMVar_ID_24880 Human_SNP_ID_707341182 A-to-I Human chrX + 299801 299801 299801 AACAGCCGAGTGTGCAGTGACTCACGCCTGTCATCCCAGCACTTTGGGAGGCGAAGGCGGGTGGA AACAGCCGAGTGTGCAGTGACTCACGCCTGTCTTCCCAGCACTTTGGGAGGCGAAGGCGGGTGGA A T PLCXD1 Ensembl:ENSG00000182378 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1449748779 Functional Loss SNV dbSNP153 33..33 33 - - - 24881 RMVar_ID_24881 Human_SNP_ID_707341236 A-to-I Human chrX + 299946 299946 299946 TGCGTGATGGGCACCTGTAGTGCCAGCTACTCAGGAGGCTGAGGCAGGAGAATGGCGTGAACCCG TGCGTGATGGGCACCTGTAGTGCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCG A G PLCXD1 Ensembl:ENSG00000182378 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1397702189 Functional Loss SNV dbSNP153 33..33 33 - - - 24882 RMVar_ID_24882 Human_SNP_ID_707341645 A-to-I Human chrX + 300592 300592 300592 ATATGTGTATGTGTACATGTATATGTGTTTATACATGTATATGTGTGTATGCGTGTATACGTGTA ATATGTGTATGTGTACATGTATATGTGTTTATGCATGTATATGTGTGTATGCGTGTATACGTGTA A G PLCXD1 Ensembl:ENSG00000182378 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs888211985 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16863268,Human_RBP_ID_17580419,Human_RBP_ID_22777552,Human_RBP_ID_26573691,Human_RBP_ID_26766873 24883 RMVar_ID_24883 Human_SNP_ID_707341702 A-to-I Human chrX + 300658 300657 300659 GTATACATGTATATGTGTGTATGCGTGTATATACACACGTATACATATATACGTGCGTGTGTATG GTATACATGTATATGTGTGTATGCGTGTATAT__ACACGTATACATATATACGTGCGTGTGTATG TAC T PLCXD1 Ensembl:ENSG00000182378 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs777367826 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_26766873,Human_RBP_ID_27792325 24884 RMVar_ID_24884 Human_SNP_ID_707341798 A-to-I Human chrX + 300883 300883 300883 GTGCCACCACACCCGACTAATTTCATATATTTAGTAGAGACGGGGTTTCTCCGCGTTGGTCAGGC GTGCCACCACACCCGACTAATTTCATATATTTGGTAGAGACGGGGTTTCTCCGCGTTGGTCAGGC A G PLCXD1 Ensembl:ENSG00000182378 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs951622923 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8276950,Human_RBP_ID_16961367,Human_RBP_ID_18149035,Human_RBP_ID_18404349,Human_RBP_ID_27792326 24885 RMVar_ID_24885 Human_SNP_ID_707341871 A-to-I Human chrX + 301074 301074 301074 TTTCTGTCACCCAGGCTGGAGGGCAGTGGTACAGTCATAGCTCACTGCAGCCTCAACCTCCTGGG TTTCTGTCACCCAGGCTGGAGGGCAGTGGTACGGTCATAGCTCACTGCAGCCTCAACCTCCTGGG A G PLCXD1 Ensembl:ENSG00000182378 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs989950772 Functional Loss SNV dbSNP153 33..33 33 - - - 24886 RMVar_ID_24886 Human_SNP_ID_707341879 A-to-I Human chrX + 301090 301090 301090 TGGAGGGCAGTGGTACAGTCATAGCTCACTGCAGCCTCAACCTCCTGGGCTCAAGCGATCCTCTC TGGAGGGCAGTGGTACAGTCATAGCTCACTGCCGCCTCAACCTCCTGGGCTCAAGCGATCCTCTC A C PLCXD1 Ensembl:ENSG00000182378 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1195763832 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1398227 24887 RMVar_ID_24887 Human_SNP_ID_707341899 A-to-I Human chrX + 301185 301185 301185 GGGACACACCCCCACTGCTGGCTAATTTTTGTATTTTTGGTAGAGTCAGGGTTTCACCACATGGC GGGACACACCCCCACTGCTGGCTAATTTTTGTGTTTTTGGTAGAGTCAGGGTTTCACCACATGGC A G PLCXD1 Ensembl:ENSG00000182378 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1215688990 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16961368 24888 RMVar_ID_24888 Human_SNP_ID_707341923 A-to-I Human chrX + 301258 301258 301258 GTCTCAAATTCCTGGGCTCCAGTGATCCTCCCACCTTAGCTTCCAGAGTGGCCAGGATCACAGGC GTCTCAAATTCCTGGGCTCCAGTGATCCTCCCGCCTTAGCTTCCAGAGTGGCCAGGATCACAGGC A G PLCXD1 Ensembl:ENSG00000182378 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1482921571 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8716970 24889 RMVar_ID_24889 Human_SNP_ID_707341949 A-to-I Human chrX + 301364 301364 301364 CGTGGTCTGGCTATGTTGTCCAGGGTGGTCTCAAACTCCTGGGCTCAACTGATCCTCCCACCTCA CGTGGTCTGGCTATGTTGTCCAGGGTGGTCTCTAACTCCTGGGCTCAACTGATCCTCCCACCTCA A T PLCXD1 Ensembl:ENSG00000182378 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1047515546 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17580421,Human_RBP_ID_22484901,Human_RBP_ID_24445168 24890 RMVar_ID_24890 Human_SNP_ID_707341957 A-to-I Human chrX + 301412 301412 301412 CTGATCCTCCCACCTCAACCTCTGCCATAGCCAGGACCTCAGGTGTCAGCCACCACACCCACAGC CTGATCCTCCCACCTCAACCTCTGCCATAGCCCGGACCTCAGGTGTCAGCCACCACACCCACAGC A C PLCXD1 Ensembl:ENSG00000182378 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1449666730 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7992599,Human_RBP_ID_17579884,Human_RBP_ID_18918328 24891 RMVar_ID_24891 Human_SNP_ID_707342059 A-to-I Human chrX + 301695 301695 301695 TCGCCCAGGCTGGAGTGCAGTGGCGCAGTCTCAGCTCACTGCAACCTCTGCCTCCCAGGTTCAAG TCGCCCAGGCTGGAGTGCAGTGGCGCAGTCTCGGCTCACTGCAACCTCTGCCTCCCAGGTTCAAG A G PLCXD1 Ensembl:ENSG00000182378 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs181064030 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_188675 24892 RMVar_ID_24892 Human_SNP_ID_707342068 A-to-I Human chrX + 301719 301719 301719 GCAGTCTCAGCTCACTGCAACCTCTGCCTCCCAGGTTCAAGCAATTCTTGTGCCTCAGCCTCCTG GCAGTCTCAGCTCACTGCAACCTCTGCCTCCCGGGTTCAAGCAATTCTTGTGCCTCAGCCTCCTG A G PLCXD1 Ensembl:ENSG00000182378 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1354205977 Functional Loss SNV dbSNP153 33..33 33 - - - 24893 RMVar_ID_24893 Human_SNP_ID_707342072 A-to-I Human chrX + 301729 301729 301729 CTCACTGCAACCTCTGCCTCCCAGGTTCAAGCAATTCTTGTGCCTCAGCCTCCTGAGTAGCTGGG CTCACTGCAACCTCTGCCTCCCAGGTTCAAGCCATTCTTGTGCCTCAGCCTCCTGAGTAGCTGGG A C PLCXD1 Ensembl:ENSG00000182378 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs374073214 Functional Loss SNV dbSNP153 33..33 33 - - - 24894 RMVar_ID_24894 Human_SNP_ID_707342073 A-to-I Human chrX + 301729 301729 301729 CTCACTGCAACCTCTGCCTCCCAGGTTCAAGCAATTCTTGTGCCTCAGCCTCCTGAGTAGCTGGG CTCACTGCAACCTCTGCCTCCCAGGTTCAAGCGATTCTTGTGCCTCAGCCTCCTGAGTAGCTGGG A G PLCXD1 Ensembl:ENSG00000182378 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs374073214 Functional Loss SNV dbSNP153 33..33 33 - - - 24895 RMVar_ID_24895 Human_SNP_ID_707342111 A-to-I Human chrX + 301826 301826 301826 TTTTGTATTTTTAGCAGAGATGGGGTTTCACCATGTTGCCCAGGCTGGTCTTGAACTCCCGACCT TTTTGTATTTTTAGCAGAGATGGGGTTTCACCGTGTTGCCCAGGCTGGTCTTGAACTCCCGACCT A G PLCXD1 Ensembl:ENSG00000182378 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1302743562 Functional Loss SNV dbSNP153 33..33 33 - - - 24896 RMVar_ID_24896 Human_SNP_ID_707342438 A-to-I Human chrX + 302699 302699 302699 GGTTCCAGCAAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTGCAGGCGCCCGCCACCACG GGTTCCAGCAAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTGCAGGCGCCCGCCACCACG A G PLCXD1 Ensembl:ENSG00000182378 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1197760865 Functional Loss SNV dbSNP153 33..33 33 - - - 24897 RMVar_ID_24897 Human_SNP_ID_707342440 A-to-I Human chrX + 302703 302703 302703 CCAGCAAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTGCAGGCGCCCGCCACCACGCCCG CCAGCAAATTCTCCTGCCTCAGCCTCCCAAGTCGCTGGGATTGCAGGCGCCCGCCACCACGCCCG A C PLCXD1 Ensembl:ENSG00000182378 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1243008133 Functional Loss SNV dbSNP153 33..33 33 - - - 24898 RMVar_ID_24898 Human_SNP_ID_707342719 A-to-I Human chrX - 303493 303492 303494 GACCTTGTGATCCGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCACC GACCTTGTGATCCGCCCACCTCGGCCTCCCA__GTGCTGGGATTACAGGCGTGAGCCACCGCACC CTT C - - Other Unknown GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1323596689 Functional Loss DEL dbSNP153 32..33 33 - - - 24899 RMVar_ID_24899 Human_SNP_ID_707342719 A-to-I Human chrX - 303494 303492 303494 TGACCTTGTGATCCGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCAC TGACCTTGTGATCCGCCCACCTCGGCCTCCCA__GTGCTGGGATTACAGGCGTGAGCCACCGCAC CTT C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1323596689 Functional Loss DEL dbSNP153 33..34 33 - - - 24900 RMVar_ID_24900 Human_SNP_ID_707342720 A-to-I Human chrX - 303494 303494 303494 TGACCTTGTGATCCGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCAC TGACCTTGTGATCCGCCCACCTCGGCCTCCCAGAGTGCTGGGATTACAGGCGTGAGCCACCGCAC T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1287735024 Functional Loss SNV dbSNP153 33..33 33 - - - 24901 RMVar_ID_24901 Human_SNP_ID_707342956 A-to-I Human chrX - 304058 304058 304058 ACAGAATCTCGCTCTGTCACCCAGGCTGGAGTACAGTGGTGCGATCTCAGTTCACTGCAACCTCT ACAGAATCTCGCTCTGTCACCCAGGCTGGAGTGCAGTGGTGCGATCTCAGTTCACTGCAACCTCT T C - - Other Unknown GSE38233;GSE112787 cultured B-cells;293 Flip-In T-REx cells,empty vector - 24183664,29967493 RNA-Seq:(High) rs888269564 Functional Loss SNV dbSNP153 33..33 33 - - - 24902 RMVar_ID_24902 Human_SNP_ID_707343176 A-to-I Human chrX - 304516 304516 304516 AAGCAGCTTCAAACCAGACCGTGAGGACGGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTG AAGCAGCTTCAAACCAGACCGTGAGGACGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTG T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs568698160 Functional Loss SNV dbSNP153 33..33 33 - - - 24903 RMVar_ID_24903 Human_SNP_ID_707351782 A-to-I Human chrX + 322605 322605 322605 GGGACGCTGAGGTGGGAGGATCACCTGAGCCCAGGAGGTGGAGGCTGCAGTGAGCTTAGATTGCA GGGACGCTGAGGTGGGAGGATCACCTGAGCCCGGGAGGTGGAGGCTGCAGTGAGCTTAGATTGCA A G LINC00685,LINC00685:2 RNACentral:URS0000D587B7,RNACentral:URS0000E2D9B0 lincRNA,lincRNA intron,exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1215491467 Functional Loss SNV dbSNP153 33..33 33 - - - 24904 RMVar_ID_24904 Human_SNP_ID_707352563 A-to-I Human chrX - 324015 324015 324015 GGCTACACACACGTCCCTGAGCTCACCACCTGAGGACGCCCTCATTCCGTCTCTATGAACAGGGC GGCTACACACACGTCCCTGAGCTCACCACCTGGGGACGCCCTCATTCCGTCTCTATGAACAGGGC T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs867299885 Functional Loss SNV dbSNP153 33..33 33 - - - 24905 RMVar_ID_24905 Human_SNP_ID_707352564 A-to-I Human chrX - 324015 324015 324015 GGCTACACACACGTCCCTGAGCTCACCACCTGAGGACGCCCTCATTCCGTCTCTATGAACAGGGC GGCTACACACACGTCCCTGAGCTCACCACCTGCGGACGCCCTCATTCCGTCTCTATGAACAGGGC T G - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs867299885 Functional Loss SNV dbSNP153 33..33 33 - - - 24906 RMVar_ID_24906 Human_SNP_ID_707358712 A-to-I Human chrX - 334413 334413 334413 CTTCGAGGCGCCCTCACCGCTGGGCGCCGTGGACCTGTACGAGTACGCATGCGGGGACGAGGACC CTTCGAGGCGCCCTCACCGCTGGGCGCCGTGGCCCTGTACGAGTACGCATGCGGGGACGAGGACC T G PPP2R3B Ensembl:ENSG00000167393 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1259331772 Functional Loss SNV dbSNP153 33..33 33 - - - 24907 RMVar_ID_24907 Human_SNP_ID_707763472 A-to-I Human chrX + 1381189 1381189 1381189 GGGAGGCCCAGGCGGGCGGACCACTTGAGGCCAGGAACTGGAGACCAGCCTGGCCAACATGGAGA GGGAGGCCCAGGCGGGCGGACCACTTGAGGCCCGGAACTGGAGACCAGCCTGGCCAACATGGAGA A C IL3RA Ensembl:ENSG00000185291 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs375535967 Functional Loss SNV dbSNP153 33..33 33 - - - 24908 RMVar_ID_24908 Human_SNP_ID_707763670 A-to-I Human chrX + 1381727 1381727 1381727 CCGACACGCCCAGCTAATTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGATGG CCGACACGCCCAGCTAATTTTGTATTTTTAGTGGAGACGGGGTTTCACCATGTTGGCCAGGATGG A G IL3RA Ensembl:ENSG00000185291 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1449761925 Functional Loss SNV dbSNP153 33..33 33 - - - 24909 RMVar_ID_24909 Human_SNP_ID_707764444 A-to-I Human chrX - 1383455 1383455 1383455 AGCCAGGCATGATGGTGCATACCTCTAATCCCAGCTACTCGAGAGGCTGAGGCAGGAGAGTTGCT AGCCAGGCATGATGGTGCATACCTCTAATCCCGGCTACTCGAGAGGCTGAGGCAGGAGAGTTGCT T C RF00017-6698,lnc-SLC25A6-4,RF00017-4643 RNACentral:URS000099749B,RNACentral:URS0000D5A2B8,RNACentral:URS00009A02E8 SRP RNA,lincRNA,SRP RNA intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1382484972 Functional Loss SNV dbSNP153 33..33 33 - - - 24910 RMVar_ID_24910 Human_SNP_ID_707764461 A-to-I Human chrX - 1383524 1383524 1383524 CTGAGGTCGGGAGTTCAGGACCAGCCTGACCAACATGGAGAAGCCCTGTCTCTACTAAAAATAAA CTGAGGTCGGGAGTTCAGGACCAGCCTGACCAGCATGGAGAAGCCCTGTCTCTACTAAAAATAAA T C RF00017-6698,lnc-SLC25A6-4,RF00017-4643 RNACentral:URS000099749B,RNACentral:URS0000D5A2B8,RNACentral:URS00009A02E8 SRP RNA,lincRNA,SRP RNA intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1398632586 Functional Loss SNV dbSNP153 33..33 33 - - - 24911 RMVar_ID_24911 Human_SNP_ID_707764528 A-to-I Human chrX - 1383776 1383776 1383776 CCTCGGCCTCCCAAAGTGCTGGGATGACAGGCATGAGTCACTGTGCCTGGCCAGTCCTGCACAAT CCTCGGCCTCCCAAAGTGCTGGGATGACAGGCCTGAGTCACTGTGCCTGGCCAGTCCTGCACAAT T G RF00017-6698,lnc-SLC25A6-4,RF00017-4643 RNACentral:URS000099749B,RNACentral:URS0000D5A2B8,RNACentral:URS00009A02E8 SRP RNA,lincRNA,SRP RNA intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1489207070 Functional Loss SNV dbSNP153 33..33 33 - - - 24912 RMVar_ID_24912 Human_SNP_ID_707764603 A-to-I Human chrX - 1383988 1383988 1383988 TCACCCAGGCTGGAGTGCTGTGGCGCAATCTCAGCTCACTGCAAGCTCCACCTCCCGGGTTCACG TCACCCAGGCTGGAGTGCTGTGGCGCAATCTCGGCTCACTGCAAGCTCCACCTCCCGGGTTCACG T C RF00017-6698,lnc-SLC25A6-4,RF00017-4643 RNACentral:URS000099749B,RNACentral:URS0000D5A2B8,RNACentral:URS00009A02E8 SRP RNA,lincRNA,SRP RNA intron,intron,intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs748251189 Functional Loss SNV dbSNP153 33..33 33 - - - 24913 RMVar_ID_24913 Human_SNP_ID_707764604 A-to-I Human chrX - 1383988 1383988 1383988 TCACCCAGGCTGGAGTGCTGTGGCGCAATCTCAGCTCACTGCAAGCTCCACCTCCCGGGTTCACG TCACCCAGGCTGGAGTGCTGTGGCGCAATCTCCGCTCACTGCAAGCTCCACCTCCCGGGTTCACG T G RF00017-6698,lnc-SLC25A6-4,RF00017-4643 RNACentral:URS000099749B,RNACentral:URS0000D5A2B8,RNACentral:URS00009A02E8 SRP RNA,lincRNA,SRP RNA intron,intron,intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs748251189 Functional Loss SNV dbSNP153 33..33 33 - - - 24914 RMVar_ID_24914 Human_SNP_ID_707764686 A-to-I Human chrX - 1384165 1384165 1384165 ATGGAGTCTCTTGTCACCCAGGCAGGACTGCAATGGTGTGGTAACGGCTCAACTCTACTTCCATC ATGGAGTCTCTTGTCACCCAGGCAGGACTGCAGTGGTGTGGTAACGGCTCAACTCTACTTCCATC T C RF00017-6698,lnc-SLC25A6-4,RF00017-4643 RNACentral:URS000099749B,RNACentral:URS0000D5A2B8,RNACentral:URS00009A02E8 SRP RNA,lincRNA,SRP RNA intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs369806609 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1712127,Human_RBP_ID_7985784,Human_RBP_ID_18916829 24915 RMVar_ID_24915 Human_SNP_ID_707765070 A-to-I Human chrX - 1385087 1385087 1385087 GGCATGCGCCACCACACCCGGCTGATTTTAGTATTTTTAGTGGAGATGGGGTTTCACCATGTTTA GGCATGCGCCACCACACCCGGCTGATTTTAGTGTTTTTAGTGGAGATGGGGTTTCACCATGTTTA T C RF00017-6698,RF00017-4643 RNACentral:URS000099749B,RNACentral:URS00009A02E8 SRP RNA,SRP RNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1416516092 Functional Loss SNV dbSNP153 33..33 33 - - - 24916 RMVar_ID_24916 Human_SNP_ID_707765106 A-to-I Human chrX - 1385157 1385157 1385157 GTGGTGCAACCTCTGCCTCCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGG GTGGTGCAACCTCTGCCTCCCAGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGG T C RF00017-6698,RF00017-4643 RNACentral:URS000099749B,RNACentral:URS00009A02E8 SRP RNA,SRP RNA intron,intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1422953799 Functional Loss SNV dbSNP153 33..33 33 - - - 24917 RMVar_ID_24917 Human_SNP_ID_707781889 A-to-I Human chrX - 1425521 1425521 1425521 CATGGGGCTCCTGGAGAAGACAGAGCAAGGTGACAGGACCCAGCGGGTTTTGCTCTGAGGATCTT CATGGGGCTCCTGGAGAAGACAGAGCAAGGTGGCAGGACCCAGCGGGTTTTGCTCTGAGGATCTT T C ASMTL Ensembl:ENSG00000169093 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs764981191 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 24918 RMVar_ID_24918 Human_SNP_ID_707782825 A-to-I Human chrX - 1428260 1428260 1428260 GGCTAATTTTTTGTATTTTTTTTAGTAGAGACAGGGTTTCACTGTGTTAGCCAGGATGGCCTCGA GGCTAATTTTTTGTATTTTTTTTAGTAGAGACGGGGTTTCACTGTGTTAGCCAGGATGGCCTCGA T C ASMTL Ensembl:ENSG00000169093 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1267362297 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4744,RMVar_hsa_circ_98632,RMVar_hsa_circ_261185,RMVar_hsa_circ_34978,RMVar_hsa_circ_70387,RMVar_hsa_circ_5630 24919 RMVar_ID_24919 Human_SNP_ID_707783235 A-to-I Human chrX - 1429459 1429459 1429459 ATACATTTAAAGAAAGACAGGCCGGGCACAGTAGCTCAAGCCAAGACGGGAGGATCACTTCATCC ATACATTTAAAGAAAGACAGGCCGGGCACAGTGGCTCAAGCCAAGACGGGAGGATCACTTCATCC T C ASMTL Ensembl:ENSG00000169093 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1329023156 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4744,RMVar_hsa_circ_98632,RMVar_hsa_circ_261185,RMVar_hsa_circ_34978,RMVar_hsa_circ_70387,RMVar_hsa_circ_5630 24920 RMVar_ID_24920 Human_SNP_ID_707783262 A-to-I Human chrX - 1429563 1429562 1429563 GAACTCCTGACCTCAGGTGATCTGCCTGCCTCAGCCTCCCGAAGTGCTGGGAGCCACCGCGCCCA GAACTCCTGACCTCAGGTGATCTGCCTGCCTC_GCCTCCCGAAGTGCTGGGAGCCACCGCGCCCA CT C ASMTL Ensembl:ENSG00000169093 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1385471485 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_4744,RMVar_hsa_circ_98632,RMVar_hsa_circ_261185,RMVar_hsa_circ_34978,RMVar_hsa_circ_70387,RMVar_hsa_circ_5630 24921 RMVar_ID_24921 Human_SNP_ID_707783444 A-to-I Human chrX - 1430179 1430179 1430179 AAATCCCAATCTCTACTAAAAATACAAAAATTAGCCCGGTGTGGTGGCAGGTGCCTGTAATCCCA AAATCCCAATCTCTACTAAAAATACAAAAATTGGCCCGGTGTGGTGGCAGGTGCCTGTAATCCCA T C ASMTL Ensembl:ENSG00000169093 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1275579392 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4744,RMVar_hsa_circ_98632,RMVar_hsa_circ_261185,RMVar_hsa_circ_34978,RMVar_hsa_circ_70387,RMVar_hsa_circ_5630 24922 RMVar_ID_24922 Human_SNP_ID_707889304 A-to-I Human chrX + 1733968 1733967 1733968 TTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGAGCAGTCTGGTCTTGAACTTCTGACCT TTTTGTATTTTTAGTAGAGATGGGGTTTCACC_TGTTGAGCAGTCTGGTCTTGAACTTCTGACCT CA C AL683807.1 Ensembl:ENSG00000223511 lincRNA exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1248151973 Functional Loss DEL dbSNP153 33..33 33 - - - Human_Splice_Rec_2182755 24923 RMVar_ID_24923 Human_SNP_ID_707889305 A-to-I Human chrX + 1733968 1733968 1733968 TTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGAGCAGTCTGGTCTTGAACTTCTGACCT TTTTGTATTTTTAGTAGAGATGGGGTTTCACCGTGTTGAGCAGTCTGGTCTTGAACTTCTGACCT A G AL683807.1 Ensembl:ENSG00000223511 lincRNA exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1285597047 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2182755 24924 RMVar_ID_24924 Human_SNP_ID_707891696 A-to-I Human chrX + 1739864 1739864 1739864 CCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGCATCTGGCCTATTCTTTAAATT CCTCGGCCTCCCAAAGTGCTGGGATTACAGGCCTGAGCCACTGCATCTGGCCTATTCTTTAAATT A C AL683807.1 Ensembl:ENSG00000223511 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1202772462 Functional Loss SNV dbSNP153 33..33 33 - - - 24925 RMVar_ID_24925 Human_SNP_ID_707892664 A-to-I Human chrX + 1742864 1742864 1742864 TCATGCCTGTAATCCTAACACTTTGGGAGGCCAAGGCGGGTAGATCACTTGAGGCCAAGAGTTCG TCATGCCTGTAATCCTAACACTTTGGGAGGCCGAGGCGGGTAGATCACTTGAGGCCAAGAGTTCG A G AL683807.1 Ensembl:ENSG00000223511 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1270425574 Functional Loss SNV dbSNP153 33..33 33 - - - 24926 RMVar_ID_24926 Human_SNP_ID_707899367 A-to-I Human chrX + 1767555 1767549 1767555 TCCATGGCACTGAAGCCTGGATAACACAGTGTAAGACCTCATCTCTAAAAATAAGAAGGAGGCCA TCCATGGCACTGAAGCCTGGATAACAC______AGACCTCATCTCTAAAAATAAGAAGGAGGCCA CAGTGTA C AL683807.2 Ensembl:ENSG00000234622 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1212250325 Functional Loss DEL dbSNP153 28..33 33 - - - 24927 RMVar_ID_24927 Human_SNP_ID_707990591 A-to-I Human chrX - 2261432 2261432 2261432 ATAAGCAGATCACATCCAGAACAACCCCACCCAACAGAAATGACAGCTACTTCCTAGAGACTTTA ATAAGCAGATCACATCCAGAACAACCCCACCCGACAGAAATGACAGCTACTTCCTAGAGACTTTA T C DHRSX Ensembl:ENSG00000169084 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs35731332 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_261193,RMVar_hsa_circ_318035,RMVar_hsa_circ_341978,RMVar_hsa_circ_82687,RMVar_hsa_circ_261191,RMVar_hsa_circ_261192 24928 RMVar_ID_24928 Human_SNP_ID_707990592 A-to-I Human chrX - 2261432 2261432 2261433 ATAAGCAGATCACATCCAGAACAACCCCACCCAACAGAAATGACAGCTACTTCCTAGAGACTTTA ATAAGCAGATCACATCCAGAACAACCCCACCTGACAGAAATGACAGCTACTTCCTAGAGACTTTA TG CA DHRSX Ensembl:ENSG00000169084 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs386823402 Functional Loss MNV dbSNP153 32..33 33 - - - RMVar_hsa_circ_261193,RMVar_hsa_circ_318035,RMVar_hsa_circ_341978,RMVar_hsa_circ_82687,RMVar_hsa_circ_261191,RMVar_hsa_circ_261192 24929 RMVar_ID_24929 Human_SNP_ID_708052177 A-to-I Human chrX - 2487523 2487523 2487523 CGTGTCTACTAAAAATACAAGAAACTAGCCAGATGCGGTGGCACCCGCCTGTAATCCCAGCTACT CGTGTCTACTAAAAATACAAGAAACTAGCCAGGTGCGGTGGCACCCGCCTGTAATCCCAGCTACT T C ZBED1,DHRSX Ensembl:ENSG00000214717,Ensembl:ENSG00000169084 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs5983102 Functional Loss SNV dbSNP153 33..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 24930 RMVar_ID_24930 Human_SNP_ID_708114622 A-to-I Human chrX + 2735947 2735947 2735947 GCTGCTGGCTTGGCACGGTGGTTCACACCTGTAATCCCAGCATTTTGGGAGGCCGAGGTGGGCAG GCTGCTGGCTTGGCACGGTGGTTCACACCTGTCATCCCAGCATTTTGGGAGGCCGAGGTGGGCAG A C CD99 Ensembl:ENSG00000002586 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1465070715 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_372135,RMVar_hsa_circ_261211,RMVar_hsa_circ_261213,RMVar_hsa_circ_115994,RMVar_hsa_circ_261214,RMVar_hsa_circ_316932 24931 RMVar_ID_24931 Human_SNP_ID_708114623 A-to-I Human chrX + 2735947 2735947 2735947 GCTGCTGGCTTGGCACGGTGGTTCACACCTGTAATCCCAGCATTTTGGGAGGCCGAGGTGGGCAG GCTGCTGGCTTGGCACGGTGGTTCACACCTGTGATCCCAGCATTTTGGGAGGCCGAGGTGGGCAG A G CD99 Ensembl:ENSG00000002586 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1465070715 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_372135,RMVar_hsa_circ_261211,RMVar_hsa_circ_261213,RMVar_hsa_circ_115994,RMVar_hsa_circ_261214,RMVar_hsa_circ_316932 24932 RMVar_ID_24932 Human_SNP_ID_708152202 A-to-I Human chrX - 2913306 2913306 2913306 ACCTTAACTCTGATAAGAAACATTTACAATCTATTTTCTCTGAAGCCTGCCACCTAGAGGCTTCA ACCTTAACTCTGATAAGAAACATTTACAATCTGTTTTCTCTGAAGCCTGCCACCTAGAGGCTTCA T C ARSD Ensembl:ENSG00000006756 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs892259730 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126023,RMVar_hsa_circ_261223 24933 RMVar_ID_24933 Human_SNP_ID_708289552 A-to-I Human chrX - 3608064 3608064 3608064 CAGTCTGGGAAACGTGGTGAGACCTCATCTCTACAAAATACAAAAAAATTAGCCGGGCATGGTGG CAGTCTGGGAAACGTGGTGAGACCTCATCTCTTCAAAATACAAAAAAATTAGCCGGGCATGGTGG T A PRKX Ensembl:ENSG00000183943 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1407970589 Functional Loss SNV dbSNP153 33..33 33 - - - 24934 RMVar_ID_24934 Human_SNP_ID_708289773 A-to-I Human chrX - 3609398 3609398 3609398 CCAGCACCTTGGGAGGCCGAGGCGCATGGATCATCTGAGGTCAGGAGTTCGAGACCAGCCTGGCA CCAGCACCTTGGGAGGCCGAGGCGCATGGATCGTCTGAGGTCAGGAGTTCGAGACCAGCCTGGCA T C PRKX Ensembl:ENSG00000183943 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985191147 Functional Loss SNV dbSNP153 33..33 33 - - - 24935 RMVar_ID_24935 Human_SNP_ID_708292559 A-to-I Human chrX - 3623504 3623503 3623505 TCACCCCGGCTGGAGTGCAGTGGCACAATCATAGCTCACTGCAGCCTCGACGTCCTGGGCTCAAA TCACCCCGGCTGGAGTGCAGTGGCACAATCA__GCTCACTGCAGCCTCGACGTCCTGGGCTCAAA CTA C PRKX Ensembl:ENSG00000183943 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs942167201 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_375429,RMVar_hsa_circ_316984,RMVar_hsa_circ_261233,RMVar_hsa_circ_51485,RMVar_hsa_circ_378096 24936 RMVar_ID_24936 Human_SNP_ID_708294763 A-to-I Human chrX - 3635405 3635405 3635405 GTGTTTCAGCAGATGAGTGAGATCATTTTTCCAATGACAGATCTGAATAGTGATGAATTTTCTTC GTGTTTCAGCAGATGAGTGAGATCATTTTTCCGATGACAGATCTGAATAGTGATGAATTTTCTTC T C PRKX Ensembl:ENSG00000183943 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs948423938 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_375429,RMVar_hsa_circ_316984,RMVar_hsa_circ_261233,RMVar_hsa_circ_38760,RMVar_hsa_circ_378096,RMVar_hsa_circ_307747,RMVar_hsa_circ_261236 24937 RMVar_ID_24937 Human_SNP_ID_708298476 A-to-I Human chrX - 3652168 3652168 3652168 GTGATGCGCCCACCTTGGCATCCCAAAGTGCTAGGATTACAGGTGTGAGCCACCGCACCCGGCCC GTGATGCGCCCACCTTGGCATCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCACCCGGCCC T C PRKX Ensembl:ENSG00000183943 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749372253 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_375429,RMVar_hsa_circ_261233,RMVar_hsa_circ_38760 24938 RMVar_ID_24938 Human_SNP_ID_708310262 A-to-I Human chrX - 3709987 3709987 3709987 GGCCGGGAGTTCCAGACCAGCCTGGGCAATATAGTGAGACCCTCATCTCTTAAAAAAAATAGTAG GGCCGGGAGTTCCAGACCAGCCTGGGCAATATGGTGAGACCCTCATCTCTTAAAAAAAATAGTAG T C PRKX Ensembl:ENSG00000183943 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs936580472 Functional Loss SNV dbSNP153 33..33 33 - - - 24939 RMVar_ID_24939 Human_SNP_ID_708330749 A-to-I Human chrX - 3813477 3813477 3813477 GGGCTAATTATTTGTAGAAATGAAGACTTCCTATGGTGCTCAGGCTGGTCTTAAACTCCTGAGCT GGGCTAATTATTTGTAGAAATGAAGACTTCCTGTGGTGCTCAGGCTGGTCTTAAACTCCTGAGCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs963241843 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16879970 24940 RMVar_ID_24940 Human_SNP_ID_708333762 A-to-I Human chrX - 3826679 3826679 3826679 GCTGGAGTACAGTGGCGCAGTCTGAGTTCACTACAGCCTCCACCTCCCAGGTTCAAGAGATTCTC GCTGGAGTACAGTGGCGCAGTCTGAGTTCACTGCAGCCTCCACCTCCCAGGTTCAAGAGATTCTC T C BX890604.2 Ensembl:ENSG00000285756 lincRNA intron GSE123020:GSM3490829,GSM3490830,GSM3490831 esophageal squamous carcinoma cells,EC109 cell line - 32596459 RNA-Seq:(High) rs1422755249 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2183350,Human_Splice_Rec_2183358,Human_Splice_Rec_2183413,Human_Splice_Rec_2183414,Human_Splice_Rec_2183437,Human_Splice_Rec_2183438 RMVar_hsa_circ_32521,RMVar_hsa_circ_261241,RMVar_hsa_circ_261243,RMVar_hsa_circ_76630,RMVar_hsa_circ_118860,RMVar_hsa_circ_261242,RMVar_hsa_circ_261244 24941 RMVar_ID_24941 Human_SNP_ID_708622163 A-to-I Human chrX - 5306863 5306863 5306863 GACCTGATACCACATGATTTGGCTAGAGCAACACTTACGGGTTTGTTGCATCAGCCCAGTGTCCC GACCTGATACCACATGATTTGGCTAGAGCAACGCTTACGGGTTTGTTGCATCAGCCCAGTGTCCC T C AC112656.1 Ensembl:ENSG00000238193 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1447813632 Functional Loss SNV dbSNP153 33..33 33 - - - 24942 RMVar_ID_24942 Human_SNP_ID_708622164 A-to-I Human chrX - 5306865 5306865 5306865 AAGACCTGATACCACATGATTTGGCTAGAGCAACACTTACGGGTTTGTTGCATCAGCCCAGTGTC AAGACCTGATACCACATGATTTGGCTAGAGCAGCACTTACGGGTTTGTTGCATCAGCCCAGTGTC T C AC112656.1 Ensembl:ENSG00000238193 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1379310689 Functional Loss SNV dbSNP153 33..33 33 - - - 24943 RMVar_ID_24943 Human_SNP_ID_708622172 A-to-I Human chrX - 5306887 5306887 5306887 TTGCTGTCAGGCACTTCGTATAAAGACCTGATACCACATGATTTGGCTAGAGCAACACTTACGGG TTGCTGTCAGGCACTTCGTATAAAGACCTGATGCCACATGATTTGGCTAGAGCAACACTTACGGG T C AC112656.1 Ensembl:ENSG00000238193 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285680702 Functional Loss SNV dbSNP153 33..33 33 - - - 24944 RMVar_ID_24944 Human_SNP_ID_708935222 A-to-I Human chrX - 6970120 6970120 6970120 TCTTTGGATCTTCATTCTGAAGCCTCCCGTGTATACACATTGATTTGTGTGTCTTTTCTCCTATT TCTTTGGATCTTCATTCTGAAGCCTCCCGTGTGTACACATTGATTTGTGTGTCTTTTCTCCTATT T C PUDP Ensembl:ENSG00000130021 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1015251009 Functional Loss SNV dbSNP153 33..33 33 - - - 24945 RMVar_ID_24945 Human_SNP_ID_708935354 A-to-I Human chrX - 6970871 6970871 6970871 AATTTTTGTAGTTTTAGTAGAGACGGGGTTTCACTATCAGGCTGGTCTTGAACTCCTAAACTCCC AATTTTTGTAGTTTTAGTAGAGACGGGGTTTCGCTATCAGGCTGGTCTTGAACTCCTAAACTCCC T C PUDP Ensembl:ENSG00000130021 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935899993 Functional Loss SNV dbSNP153 33..33 33 - - - 24946 RMVar_ID_24946 Human_SNP_ID_708969564 A-to-I Human chrX + 7172284 7172284 7172284 GCATCCTTAAGGGACCCAGAATGAAATTGCTCAGGCATGGGGAAATAACATCCATGTGTTCTGGA GCATCCTTAAGGGACCCAGAATGAAATTGCTCCGGCATGGGGAAATAACATCCATGTGTTCTGGA A C STS Ensembl:ENSG00000101846 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1374029798 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48217 24947 RMVar_ID_24947 Human_SNP_ID_708982347 A-to-I Human chrX + 7242541 7242541 7242541 AGGATTGCTTGAGCCCGGGAGGTTGAGGCTGCAGTGAGCCGTGATCACGCCACTGCACTCCAGCC AGGATTGCTTGAGCCCGGGAGGTTGAGGCTGCGGTGAGCCGTGATCACGCCACTGCACTCCAGCC A G STS Ensembl:ENSG00000101846 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs999205165 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_261265,RMVar_hsa_circ_124224,RMVar_hsa_circ_341273 24948 RMVar_ID_24948 Human_SNP_ID_709107135 A-to-I Human chrX + 7971612 7971612 7971612 CAAGAGGTTGCATGACTCCTAAACAGTAATTTATAATCTTAAAGCTACTTTGTTAGTCCTACAAA CAAGAGGTTGCATGACTCCTAAACAGTAATTTGTAATCTTAAAGCTACTTTGTTAGTCCTACAAA A G AC079142.1 Ensembl:ENSG00000285679 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs780870714 Functional Loss SNV dbSNP153 33..33 33 - - - 24949 RMVar_ID_24949 Human_SNP_ID_709107136 A-to-I Human chrX + 7971614 7971614 7971614 AGAGGTTGCATGACTCCTAAACAGTAATTTATAATCTTAAAGCTACTTTGTTAGTCCTACAAAGG AGAGGTTGCATGACTCCTAAACAGTAATTTATGATCTTAAAGCTACTTTGTTAGTCCTACAAAGG A G AC079142.1 Ensembl:ENSG00000285679 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1407714928 Functional Loss SNV dbSNP153 33..33 33 - - - 24950 RMVar_ID_24950 Human_SNP_ID_709107147 A-to-I Human chrX + 7971744 7971744 7971744 TTAAATGAGAAACTAAATTTCTTCCCAAGGTTAGTTCGGCCTATGTCCAGGAATGAACAAGGACA TTAAATGAGAAACTAAATTTCTTCCCAAGGTTGGTTCGGCCTATGTCCAGGAATGAACAAGGACA A G AC079142.1 Ensembl:ENSG00000285679 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1347261975 Functional Loss SNV dbSNP153 33..33 33 - - - 24951 RMVar_ID_24951 Human_SNP_ID_709262973 A-to-I Human chrX - 8856892 8856892 8856892 CAGCAGCATCAGACCTGGCTCGAAAGCATCACAGAGAAAGACAACAATCTGGTTCCTATTGGCAA CAGCAGCATCAGACCTGGCTCGAAAGCATCACGGAGAAAGACAACAATCTGGTTCCTATTGGCAA T C AC003685.2 Ensembl:ENSG00000231619 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1198612139 Functional Loss SNV dbSNP153 33..33 33 - - - 24952 RMVar_ID_24952 Human_SNP_ID_709262974 A-to-I Human chrX - 8856894 8856894 8856894 AACAGCAGCATCAGACCTGGCTCGAAAGCATCACAGAGAAAGACAACAATCTGGTTCCTATTGGC AACAGCAGCATCAGACCTGGCTCGAAAGCATCGCAGAGAAAGACAACAATCTGGTTCCTATTGGC T C AC003685.2 Ensembl:ENSG00000231619 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1482893944 Functional Loss SNV dbSNP153 33..33 33 - - - 24953 RMVar_ID_24953 Human_SNP_ID_709262980 A-to-I Human chrX - 8856912 8856912 8856912 CAGAGCTGCAGCAGCAGGAACAGCAGCATCAGACCTGGCTCGAAAGCATCACAGAGAAAGACAAC CAGAGCTGCAGCAGCAGGAACAGCAGCATCAGGCCTGGCTCGAAAGCATCACAGAGAAAGACAAC T C AC003685.2 Ensembl:ENSG00000231619 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1383548494 Functional Loss SNV dbSNP153 33..33 33 - - - 24954 RMVar_ID_24954 Human_SNP_ID_709311804 A-to-I Human chrX - 9125966 9125966 9125966 TGTATGTTTTTGTAGAAATGGGGCCTCACTATATTGCCTAGGTGGGTCTCAAACTCCTGGGCTCA TGTATGTTTTTGTAGAAATGGGGCCTCACTATGTTGCCTAGGTGGGTCTCAAACTCCTGGGCTCA T C FAM9B Ensembl:ENSG00000177138 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1024146252 Functional Loss SNV dbSNP153 33..33 33 - - - 24955 RMVar_ID_24955 Human_SNP_ID_709386296 A-to-I Human chrX + 9509754 9509754 9509754 GCGATCAGCCCACCTCGGCCTTTCAAAATGCTAGGTTTACAGGTATGAGCCACTGTGCCTGGTCT GCGATCAGCCCACCTCGGCCTTTCAAAATGCTGGGTTTACAGGTATGAGCCACTGTGCCTGGTCT A G TBL1X Ensembl:ENSG00000101849 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006602523 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9222,RMVar_hsa_circ_6753 24956 RMVar_ID_24956 Human_SNP_ID_709393098 A-to-I Human chrX + 9545532 9545532 9545532 GCGCCACTGCACTCCATCCTGGGTGACAAAGCAAAACTCCATCTCAAGAAAAAAAAAAAAATTCA GCGCCACTGCACTCCATCCTGGGTGACAAAGCTAAACTCCATCTCAAGAAAAAAAAAAAAATTCA A T TBL1X Ensembl:ENSG00000101849 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749735253 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9222 24957 RMVar_ID_24957 Human_SNP_ID_709393250 A-to-I Human chrX + 9546331 9546331 9546331 GTCAGGAGATCGAGACCCATCCTGGCTAACACAGTGAAACCCCATTTCTACTAAAAGTACAAAAA GTCAGGAGATCGAGACCCATCCTGGCTAACACGGTGAAACCCCATTTCTACTAAAAGTACAAAAA A G TBL1X Ensembl:ENSG00000101849 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs775424891 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9222 24958 RMVar_ID_24958 Human_SNP_ID_709407883 A-to-I Human chrX + 9622492 9622492 9622492 TTTTTTTTGTTTTTGAAACTAAGTCTCACTCTATCACCCAGGCTGGAGTGCAGTGGTACAATTTC TTTTTTTTGTTTTTGAAACTAAGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGTACAATTTC A G TBL1X Ensembl:ENSG00000101849 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs901436246 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9222 24959 RMVar_ID_24959 Human_SNP_ID_709487053 A-to-I Human chrX + 10019663 10019663 10019663 TTTACGTGTGTGTCTTGCAGGGTTATTTGGGTATTATCCTATAGATGGACTGAGTGTTTGAAACC TTTACGTGTGTGTCTTGCAGGGTTATTTGGGTGTTATCCTATAGATGGACTGAGTGTTTGAAACC A G WWC3 Ensembl:ENSG00000047644 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1307770676 Functional Loss SNV dbSNP153 33..33 33 - - - 24960 RMVar_ID_24960 Human_SNP_ID_709487275 A-to-I Human chrX + 10021051 10021051 10021051 AACATAACTGTTAAAGACAGTGAATCTTTACAAAAGAGGCAAAAGTGTTCTTCCCATATTTTCTG AACATAACTGTTAAAGACAGTGAATCTTTACAGAAGAGGCAAAAGTGTTCTTCCCATATTTTCTG A G WWC3 Ensembl:ENSG00000047644 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs938920453 Functional Loss SNV dbSNP153 33..33 33 - - - 24961 RMVar_ID_24961 Human_SNP_ID_709489955 A-to-I Human chrX + 10036600 10036600 10036600 CCTTCTGTCTTTATGGATTTGCCTATTCATGCAGGAAATCTGAGGAGCGAGATCGATCTCAAGAT CCTTCTGTCTTTATGGATTTGCCTATTCATGCGGGAAATCTGAGGAGCGAGATCGATCTCAAGAT A G WWC3 Ensembl:ENSG00000047644 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893723584 Functional Loss SNV dbSNP153 33..33 33 - - - 24962 RMVar_ID_24962 Human_SNP_ID_709521243 A-to-I Human chrX + 10211155 10211155 10211155 GGGCGTGGTGACACACGCCTGTGGTCCCAGCTACTCGGGAGGCTGAGGCATAAGAATCACTTGAA GGGCGTGGTGACACACGCCTGTGGTCCCAGCTGCTCGGGAGGCTGAGGCATAAGAATCACTTGAA A G CLCN4 Ensembl:ENSG00000073464 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1466794387 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_361498,RMVar_hsa_circ_17658 24963 RMVar_ID_24963 Human_SNP_ID_709566631 A-to-I Human chrX - 10470351 10470351 10470351 TTGGGTTACAGCCCAAATCTGACCCTCTACCTATATTTGTAAATAAAGTTTTATTGGAACCTGGC TTGGGTTACAGCCCAAATCTGACCCTCTACCTGTATTTGTAAATAAAGTTTTATTGGAACCTGGC T C MID1 Ensembl:ENSG00000101871 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1409890033 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1696,RMVar_hsa_circ_353430,RMVar_hsa_circ_261316,RMVar_hsa_circ_359561,RMVar_hsa_circ_363543,RMVar_hsa_circ_324549,RMVar_hsa_circ_261315 24964 RMVar_ID_24964 Human_SNP_ID_709572922 A-to-I Human chrX - 10511459 10511459 10511459 GGATCACTAGAACCCAGAAGAAGTTGGAGATTACAGTGATCTATGATTGTACCACTGGACTCCAG GGATCACTAGAACCCAGAAGAAGTTGGAGATTCCAGTGATCTATGATTGTACCACTGGACTCCAG T G MID1 Ensembl:ENSG00000101871 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1322439690 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_353430,RMVar_hsa_circ_72884,RMVar_hsa_circ_261316,RMVar_hsa_circ_359561,RMVar_hsa_circ_324549,RMVar_hsa_circ_357306,RMVar_hsa_circ_261315,RMVar_hsa_circ_358411,RMVar_hsa_circ_347863,RMVar_hsa_circ_334723,RMVar_hsa_circ_261319,RMVar_hsa_circ_1425 24965 RMVar_ID_24965 Human_SNP_ID_709649742 A-to-I Human chrX - 10972141 10972141 10972141 CTTTGTGGGGCATTAAGACAAGTAGAGCCACAAGAGTCAATTTGTTTTTGCTATTTTGATTTAAG CTTTGTGGGGCATTAAGACAAGTAGAGCCACAGGAGTCAATTTGTTTTTGCTATTTTGATTTAAG T C AC073529.1 Ensembl:ENSG00000234129 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1193873380 Functional Loss SNV dbSNP153 33..33 33 - - - 24966 RMVar_ID_24966 Human_SNP_ID_709649745 A-to-I Human chrX - 10972150 10972150 10972150 TCTCAGTGACTTTGTGGGGCATTAAGACAAGTAGAGCCACAAGAGTCAATTTGTTTTTGCTATTT TCTCAGTGACTTTGTGGGGCATTAAGACAAGTTGAGCCACAAGAGTCAATTTGTTTTTGCTATTT T A AC073529.1 Ensembl:ENSG00000234129 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965317166 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3237453 24967 RMVar_ID_24967 Human_SNP_ID_709725310 A-to-I Human chrX - 11407375 11407375 11407375 TCCATCCTAACTGATTAACAGATAAACAAAATATGGTCAACCATACAAGAGAATATTATTCAATA TCCATCCTAACTGATTAACAGATAAACAAAATGTGGTCAACCATACAAGAGAATATTATTCAATA T C ARHGAP6 Ensembl:ENSG00000047648 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935030480 Functional Loss SNV dbSNP153 33..33 33 - - - 24968 RMVar_ID_24968 Human_SNP_ID_709741574 A-to-I Human chrX - 11501792 11501792 11501792 TAAAGATGATGAGGATGAAGACCTTTATGACTATCCACTCCTACTTAATGAATAGTAAATATATT TAAAGATGATGAGGATGAAGACCTTTATGACTGTCCACTCCTACTTAATGAATAGTAAATATATT T C ARHGAP6 Ensembl:ENSG00000047648 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs748695000 Functional Loss SNV dbSNP153 33..33 33 - - - 24969 RMVar_ID_24969 Human_SNP_ID_710118489 A-to-I Human chrX + 13691539 13691539 13691539 AAAATTAGCCAGGCGTGGTGGCGGATGCCCGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA AAAATTAGCCAGGCGTGGTGGCGGATGCCCGTTATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA A T RAB9A Ensembl:ENSG00000123595 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170746302 Functional Loss SNV dbSNP153 33..33 33 - - - 24970 RMVar_ID_24970 Human_SNP_ID_710161349 A-to-I Human chrX - 13915160 13915160 13915160 GAGCTCAAGTGATCCTGCCACTTCAGCCTCCCAAGTAGCTGGAACTACAGGGGCACACCACCACG GAGCTCAAGTGATCCTGCCACTTCAGCCTCCCGAGTAGCTGGAACTACAGGGGCACACCACCACG T C GPM6B Ensembl:ENSG00000046653 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs901210751 Functional Loss SNV dbSNP153 33..33 33 - - - 24971 RMVar_ID_24971 Human_SNP_ID_710162200 A-to-I Human chrX - 13920101 13920101 13920101 GTGCCACCACGCCTGGCTAGTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCGGGC GTGCCACCACGCCTGGCTAGTTTTGTATTTTTGGTAGAGATGGGGTTTCACCATGTTGGCCGGGC T C GPM6B Ensembl:ENSG00000046653 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1410515732 Functional Loss SNV dbSNP153 33..33 33 - - - 24972 RMVar_ID_24972 Human_SNP_ID_710163203 A-to-I Human chrX - 13925529 13925529 13925529 GAGGATCACTTGGGGCCAGGAGTTTGAGCAACATAGCGAGACCCCATCTCTACCAAAAAAAAAAA GAGGATCACTTGGGGCCAGGAGTTTGAGCAACGTAGCGAGACCCCATCTCTACCAAAAAAAAAAA T C GPM6B Ensembl:ENSG00000046653 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1340462902 Functional Loss SNV dbSNP153 33..33 33 - - - 24973 RMVar_ID_24973 Human_SNP_ID_162458028 A-to-I Human chr3 - 168057294 168057292 168057294 GGGTGTATTATTTCATTTTCATGCTGCTGATAAAGACATACCCAAGACTGGGCAGTTTACAAAAG GGGTGTATTATTTCATTTTCATGCTGCTGATA__GACATACCCAAGACTGGGCAGTTTACAAAAG CTT C GOLIM4 Ensembl:ENSG00000173905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1179647076 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_222514 24974 RMVar_ID_24974 Human_SNP_ID_162458029 A-to-I Human chr3 - 168057294 168057294 168057294 GGGTGTATTATTTCATTTTCATGCTGCTGATAAAGACATACCCAAGACTGGGCAGTTTACAAAAG GGGTGTATTATTTCATTTTCATGCTGCTGATAGAGACATACCCAAGACTGGGCAGTTTACAAAAG T C GOLIM4 Ensembl:ENSG00000173905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1560094958 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_222514 24975 RMVar_ID_24975 Human_SNP_ID_162531982 A-to-I Human chr3 - 168368478 168368478 168368478 AAACTCCTGACCACAAGTGATCCACCCACCTCAGCCTCCCAAAGTGCTGGGACCACAGGCGTAAG AAACTCCTGACCACAAGTGATCCACCCACCTCTGCCTCCCAAAGTGCTGGGACCACAGGCGTAAG T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs770365602 Functional Loss SNV dbSNP153 33..33 33 - - - 24976 RMVar_ID_24976 Human_SNP_ID_162871846 A-to-I Human chr3 + 169778009 169778009 169778009 CTAGCACTTTGGGAGCCCAAGGTGGGAGGATCACTTGAGGCCAGGAGTTCGAGACCAGCCTGGGC CTAGCACTTTGGGAGCCCAAGGTGGGAGGATCGCTTGAGGCCAGGAGTTCGAGACCAGCCTGGGC A G MYNN Ensembl:ENSG00000085274 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs901219659 Functional Loss SNV dbSNP153 33..33 33 - - - 24977 RMVar_ID_24977 Human_SNP_ID_162871847 A-to-I Human chr3 + 169778009 169778009 169778009 CTAGCACTTTGGGAGCCCAAGGTGGGAGGATCACTTGAGGCCAGGAGTTCGAGACCAGCCTGGGC CTAGCACTTTGGGAGCCCAAGGTGGGAGGATCTCTTGAGGCCAGGAGTTCGAGACCAGCCTGGGC A T MYNN Ensembl:ENSG00000085274 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs901219659 Functional Loss SNV dbSNP153 33..33 33 - - - 24978 RMVar_ID_24978 Human_SNP_ID_162921857 A-to-I Human chr3 + 169986865 169986861 169986866 CTCCCACATCAGCCTACTGAGTAGCTGGAACTATAGGCACACTCCACTACACCCCGCTAATTTTT CTCCCACATCAGCCTACTGAGTAGCTGGA_____AGGCACACTCCACTACACCCCGCTAATTTTT AACTAT A SEC62 Ensembl:ENSG00000008952 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1366504247 Functional Loss DEL dbSNP153 30..34 33 - - - RMVar_hsa_circ_282595,RMVar_hsa_circ_91619,RMVar_hsa_circ_222545,RMVar_hsa_circ_222546,RMVar_hsa_circ_274990,RMVar_hsa_circ_93311,RMVar_hsa_circ_222549,RMVar_hsa_circ_222550,RMVar_hsa_circ_323185,RMVar_hsa_circ_222551,RMVar_hsa_circ_336288 24979 RMVar_ID_24979 Human_SNP_ID_162921923 A-to-I Human chr3 + 169987185 169987185 169987185 TCAGTGGCTCACACTTGTAATCCTAACACTTTAGGAGGCCAAGGCAGGGAGATGGCTTGAATCCA TCAGTGGCTCACACTTGTAATCCTAACACTTTGGGAGGCCAAGGCAGGGAGATGGCTTGAATCCA A G SEC62 Ensembl:ENSG00000008952 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs904656884 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_282595,RMVar_hsa_circ_91619,RMVar_hsa_circ_222545,RMVar_hsa_circ_222546,RMVar_hsa_circ_274990,RMVar_hsa_circ_93311,RMVar_hsa_circ_222549,RMVar_hsa_circ_222550,RMVar_hsa_circ_323185,RMVar_hsa_circ_222551,RMVar_hsa_circ_336288 24980 RMVar_ID_24980 Human_SNP_ID_162921933 A-to-I Human chr3 + 169987226 169987225 169987226 AGGCAGGGAGATGGCTTGAATCCAAGGGTTCGAAACCAGCCTAGGCAACATGGCGAAACCTCGTT AGGCAGGGAGATGGCTTGAATCCAAGGGTTCG_AACCAGCCTAGGCAACATGGCGAAACCTCGTT GA G SEC62 Ensembl:ENSG00000008952 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1234950155 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_282595,RMVar_hsa_circ_91619,RMVar_hsa_circ_222545,RMVar_hsa_circ_222546,RMVar_hsa_circ_274990,RMVar_hsa_circ_93311,RMVar_hsa_circ_222549,RMVar_hsa_circ_222550,RMVar_hsa_circ_323185,RMVar_hsa_circ_222551,RMVar_hsa_circ_336288 24981 RMVar_ID_24981 Human_SNP_ID_162921938 A-to-I Human chr3 + 169987236 169987236 169987236 ATGGCTTGAATCCAAGGGTTCGAAACCAGCCTAGGCAACATGGCGAAACCTCGTTTCTACAAAAA ATGGCTTGAATCCAAGGGTTCGAAACCAGCCTGGGCAACATGGCGAAACCTCGTTTCTACAAAAA A G SEC62 Ensembl:ENSG00000008952 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1025031170 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_282595,RMVar_hsa_circ_91619,RMVar_hsa_circ_222545,RMVar_hsa_circ_222546,RMVar_hsa_circ_274990,RMVar_hsa_circ_93311,RMVar_hsa_circ_222549,RMVar_hsa_circ_222550,RMVar_hsa_circ_323185,RMVar_hsa_circ_222551,RMVar_hsa_circ_336288 24982 RMVar_ID_24982 Human_SNP_ID_162921970 A-to-I Human chr3 + 169987368 169987368 169987368 CTAAGCTCAGGAGGTCGAGGCTGTCGTGAGCCAAGATCATGCCACTGTACTGCAGCCTGGGTGAC CTAAGCTCAGGAGGTCGAGGCTGTCGTGAGCCGAGATCATGCCACTGTACTGCAGCCTGGGTGAC A G SEC62 Ensembl:ENSG00000008952 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1559967264 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_282595,RMVar_hsa_circ_91619,RMVar_hsa_circ_222545,RMVar_hsa_circ_222546,RMVar_hsa_circ_274990,RMVar_hsa_circ_93311,RMVar_hsa_circ_222549,RMVar_hsa_circ_222550,RMVar_hsa_circ_323185,RMVar_hsa_circ_222551,RMVar_hsa_circ_336288 24983 RMVar_ID_24983 Human_SNP_ID_162922390 A-to-I Human chr3 + 169989274 169989274 169989274 TTTCATCATGCCTGGCTTTTTGTGGGGGAGATAGGGTATCACTCTGCCCAGGCTAGTCTCGAACT TTTCATCATGCCTGGCTTTTTGTGGGGGAGATGGGGTATCACTCTGCCCAGGCTAGTCTCGAACT A G SEC62 Ensembl:ENSG00000008952 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs921522488 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91619,RMVar_hsa_circ_222546,RMVar_hsa_circ_93311,RMVar_hsa_circ_222550 24984 RMVar_ID_24984 Human_SNP_ID_162922391 A-to-I Human chr3 + 169989274 169989274 169989274 TTTCATCATGCCTGGCTTTTTGTGGGGGAGATAGGGTATCACTCTGCCCAGGCTAGTCTCGAACT TTTCATCATGCCTGGCTTTTTGTGGGGGAGATTGGGTATCACTCTGCCCAGGCTAGTCTCGAACT A T SEC62 Ensembl:ENSG00000008952 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs921522488 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91619,RMVar_hsa_circ_222546,RMVar_hsa_circ_93311,RMVar_hsa_circ_222550 24985 RMVar_ID_24985 Human_SNP_ID_162945863 A-to-I Human chr3 - 170089720 170089720 170089720 TAGAGACGGGGCTTCACCATGTTGGCCAGGCTAGTCTCGAACTCTTGACCTCAAGTGATCCACCT TAGAGACGGGGCTTCACCATGTTGGCCAGGCTGGTCTCGAACTCTTGACCTCAAGTGATCCACCT T C PHC3 Ensembl:ENSG00000173889 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1301860854 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112414,RMVar_hsa_circ_222554 24986 RMVar_ID_24986 Human_SNP_ID_162953957 A-to-I Human chr3 - 170123554 170123554 170123554 GAACTCCTGACCTCCGGTGATCCACCCACCTCAGCCTCCCAGAGTGCTGGATTGCAGGCACGAGC GAACTCCTGACCTCCGGTGATCCACCCACCTCGGCCTCCCAGAGTGCTGGATTGCAGGCACGAGC T C PHC3 Ensembl:ENSG00000173889 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs573801843 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25713270 RMVar_hsa_circ_121381,RMVar_hsa_circ_112414,RMVar_hsa_circ_222554,RMVar_hsa_circ_222556,RMVar_hsa_circ_369993,RMVar_hsa_circ_125405,RMVar_hsa_circ_104786,RMVar_hsa_circ_84926,RMVar_hsa_circ_6537,RMVar_hsa_circ_222569,RMVar_hsa_circ_95793,RMVar_hsa_circ_222562,RMVar_hsa_circ_222564,RMVar_hsa_circ_222563,RMVar_hsa_circ_222560,RMVar_hsa_circ_222561,RMVar_hsa_circ_101805,RMVar_hsa_circ_79283,RMVar_hsa_circ_222567,RMVar_hsa_circ_222568,RMVar_hsa_circ_362889,RMVar_hsa_circ_82255,RMVar_hsa_circ_222570,RMVar_hsa_circ_222577,RMVar_hsa_circ_323156,RMVar_hsa_circ_352667,RMVar_hsa_circ_331892,RMVar_hsa_circ_312950,RMVar_hsa_circ_273803,RMVar_hsa_circ_222578,RMVar_hsa_circ_222575,RMVar_hsa_circ_222576,RMVar_hsa_circ_127197,RMVar_hsa_circ_307195,RMVar_hsa_circ_222581,RMVar_hsa_circ_301876,RMVar_hsa_circ_362739,RMVar_hsa_circ_368710,RMVar_hsa_circ_332746,RMVar_hsa_circ_89040,RMVar_hsa_circ_80345,RMVar_hsa_circ_222582,RMVar_hsa_circ_222584,RMVar_hsa_circ_222585,RMVar_hsa_circ_222583 24987 RMVar_ID_24987 Human_SNP_ID_162953998 A-to-I Human chr3 - 170123710 170123710 170123710 TGGCTCACTGCAACCTCTGCCTCCCAGGTTCAAGTGATGTTCTTGATTCAGCCTCCCAAGTAGCT TGGCTCACTGCAACCTCTGCCTCCCAGGTTCAGGTGATGTTCTTGATTCAGCCTCCCAAGTAGCT T C PHC3 Ensembl:ENSG00000173889 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1325393539 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121381,RMVar_hsa_circ_112414,RMVar_hsa_circ_222554,RMVar_hsa_circ_222556,RMVar_hsa_circ_369993,RMVar_hsa_circ_125405,RMVar_hsa_circ_104786,RMVar_hsa_circ_84926,RMVar_hsa_circ_6537,RMVar_hsa_circ_222569,RMVar_hsa_circ_95793,RMVar_hsa_circ_222562,RMVar_hsa_circ_222564,RMVar_hsa_circ_222563,RMVar_hsa_circ_222560,RMVar_hsa_circ_222561,RMVar_hsa_circ_101805,RMVar_hsa_circ_79283,RMVar_hsa_circ_222567,RMVar_hsa_circ_222568,RMVar_hsa_circ_362889,RMVar_hsa_circ_82255,RMVar_hsa_circ_222570,RMVar_hsa_circ_222577,RMVar_hsa_circ_323156,RMVar_hsa_circ_352667,RMVar_hsa_circ_331892,RMVar_hsa_circ_312950,RMVar_hsa_circ_273803,RMVar_hsa_circ_222578,RMVar_hsa_circ_222575,RMVar_hsa_circ_222576,RMVar_hsa_circ_127197,RMVar_hsa_circ_307195,RMVar_hsa_circ_222581,RMVar_hsa_circ_301876,RMVar_hsa_circ_362739,RMVar_hsa_circ_368710,RMVar_hsa_circ_332746,RMVar_hsa_circ_89040,RMVar_hsa_circ_80345,RMVar_hsa_circ_222582,RMVar_hsa_circ_222584,RMVar_hsa_circ_222585,RMVar_hsa_circ_222583 24988 RMVar_ID_24988 Human_SNP_ID_162954208 A-to-I Human chr3 - 170124507 170124507 170124507 CATTTTAAAATGAGCTGGGTGTGTTAGTGAACACCTGTGGTCCCAGCTACTCAGGAGGCTGAGCT CATTTTAAAATGAGCTGGGTGTGTTAGTGAACGCCTGTGGTCCCAGCTACTCAGGAGGCTGAGCT T C PHC3 Ensembl:ENSG00000173889 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251636460 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121381,RMVar_hsa_circ_112414,RMVar_hsa_circ_222554,RMVar_hsa_circ_222556,RMVar_hsa_circ_369993,RMVar_hsa_circ_125405,RMVar_hsa_circ_104786,RMVar_hsa_circ_84926,RMVar_hsa_circ_6537,RMVar_hsa_circ_222569,RMVar_hsa_circ_95793,RMVar_hsa_circ_222562,RMVar_hsa_circ_222564,RMVar_hsa_circ_222563,RMVar_hsa_circ_222560,RMVar_hsa_circ_222561,RMVar_hsa_circ_101805,RMVar_hsa_circ_79283,RMVar_hsa_circ_222567,RMVar_hsa_circ_222568,RMVar_hsa_circ_362889,RMVar_hsa_circ_82255,RMVar_hsa_circ_222570,RMVar_hsa_circ_222577,RMVar_hsa_circ_323156,RMVar_hsa_circ_352667,RMVar_hsa_circ_331892,RMVar_hsa_circ_312950,RMVar_hsa_circ_273803,RMVar_hsa_circ_222578,RMVar_hsa_circ_222575,RMVar_hsa_circ_222576,RMVar_hsa_circ_127197,RMVar_hsa_circ_307195,RMVar_hsa_circ_222581,RMVar_hsa_circ_301876,RMVar_hsa_circ_362739,RMVar_hsa_circ_368710,RMVar_hsa_circ_332746,RMVar_hsa_circ_89040,RMVar_hsa_circ_80345,RMVar_hsa_circ_222582,RMVar_hsa_circ_222584,RMVar_hsa_circ_222585,RMVar_hsa_circ_222583 24989 RMVar_ID_24989 Human_SNP_ID_162954210 A-to-I Human chr3 - 170124514 170124514 170124514 CAAAAAACATTTTAAAATGAGCTGGGTGTGTTAGTGAACACCTGTGGTCCCAGCTACTCAGGAGG CAAAAAACATTTTAAAATGAGCTGGGTGTGTTGGTGAACACCTGTGGTCCCAGCTACTCAGGAGG T C PHC3 Ensembl:ENSG00000173889 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1212910056 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121381,RMVar_hsa_circ_112414,RMVar_hsa_circ_222554,RMVar_hsa_circ_222556,RMVar_hsa_circ_369993,RMVar_hsa_circ_125405,RMVar_hsa_circ_104786,RMVar_hsa_circ_84926,RMVar_hsa_circ_6537,RMVar_hsa_circ_222569,RMVar_hsa_circ_95793,RMVar_hsa_circ_222562,RMVar_hsa_circ_222564,RMVar_hsa_circ_222563,RMVar_hsa_circ_222560,RMVar_hsa_circ_222561,RMVar_hsa_circ_101805,RMVar_hsa_circ_79283,RMVar_hsa_circ_222567,RMVar_hsa_circ_222568,RMVar_hsa_circ_362889,RMVar_hsa_circ_82255,RMVar_hsa_circ_222570,RMVar_hsa_circ_222577,RMVar_hsa_circ_323156,RMVar_hsa_circ_352667,RMVar_hsa_circ_331892,RMVar_hsa_circ_312950,RMVar_hsa_circ_273803,RMVar_hsa_circ_222578,RMVar_hsa_circ_222575,RMVar_hsa_circ_222576,RMVar_hsa_circ_127197,RMVar_hsa_circ_307195,RMVar_hsa_circ_222581,RMVar_hsa_circ_301876,RMVar_hsa_circ_362739,RMVar_hsa_circ_368710,RMVar_hsa_circ_332746,RMVar_hsa_circ_89040,RMVar_hsa_circ_80345,RMVar_hsa_circ_222582,RMVar_hsa_circ_222584,RMVar_hsa_circ_222585,RMVar_hsa_circ_222583 24990 RMVar_ID_24990 Human_SNP_ID_162954232 A-to-I Human chr3 - 170124646 170124646 170124646 TAACATTTGTGGGGCTAGGTGTGCAGTGGCTCATGCCTATAATCCCAGCACTTTGAGAGGCCAAG TAACATTTGTGGGGCTAGGTGTGCAGTGGCTCGTGCCTATAATCCCAGCACTTTGAGAGGCCAAG T C PHC3 Ensembl:ENSG00000173889 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1389516037 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7154930,Human_RBP_ID_14718988,Human_RBP_ID_23020198,Human_RBP_ID_23983835 RMVar_hsa_circ_121381,RMVar_hsa_circ_112414,RMVar_hsa_circ_222554,RMVar_hsa_circ_222556,RMVar_hsa_circ_369993,RMVar_hsa_circ_125405,RMVar_hsa_circ_104786,RMVar_hsa_circ_84926,RMVar_hsa_circ_6537,RMVar_hsa_circ_222569,RMVar_hsa_circ_95793,RMVar_hsa_circ_222562,RMVar_hsa_circ_222564,RMVar_hsa_circ_222563,RMVar_hsa_circ_222560,RMVar_hsa_circ_222561,RMVar_hsa_circ_101805,RMVar_hsa_circ_79283,RMVar_hsa_circ_222567,RMVar_hsa_circ_222568,RMVar_hsa_circ_362889,RMVar_hsa_circ_82255,RMVar_hsa_circ_222570,RMVar_hsa_circ_222577,RMVar_hsa_circ_323156,RMVar_hsa_circ_352667,RMVar_hsa_circ_331892,RMVar_hsa_circ_312950,RMVar_hsa_circ_273803,RMVar_hsa_circ_222578,RMVar_hsa_circ_222575,RMVar_hsa_circ_222576,RMVar_hsa_circ_127197,RMVar_hsa_circ_307195,RMVar_hsa_circ_222581,RMVar_hsa_circ_301876,RMVar_hsa_circ_362739,RMVar_hsa_circ_368710,RMVar_hsa_circ_332746,RMVar_hsa_circ_89040,RMVar_hsa_circ_80345,RMVar_hsa_circ_222582,RMVar_hsa_circ_222584,RMVar_hsa_circ_222585,RMVar_hsa_circ_222583 24991 RMVar_ID_24991 Human_SNP_ID_162956176 A-to-I Human chr3 - 170131668 170131668 170131668 TACCAAGCCCGGCTAATTTTTGTATTGTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGG TACCAAGCCCGGCTAATTTTTGTATTGTTAGTGGAGATGGGGTTTCACCATGTTGGCCAGGCTGG T C PHC3 Ensembl:ENSG00000173889 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1455306921 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121381,RMVar_hsa_circ_112414,RMVar_hsa_circ_222554,RMVar_hsa_circ_369993,RMVar_hsa_circ_104786,RMVar_hsa_circ_84926,RMVar_hsa_circ_6537,RMVar_hsa_circ_222569,RMVar_hsa_circ_95793,RMVar_hsa_circ_222562,RMVar_hsa_circ_222563,RMVar_hsa_circ_222560,RMVar_hsa_circ_222561,RMVar_hsa_circ_101805,RMVar_hsa_circ_222567,RMVar_hsa_circ_222568,RMVar_hsa_circ_362889,RMVar_hsa_circ_82255,RMVar_hsa_circ_222577,RMVar_hsa_circ_323156,RMVar_hsa_circ_352667,RMVar_hsa_circ_312950,RMVar_hsa_circ_273803,RMVar_hsa_circ_222578,RMVar_hsa_circ_222576,RMVar_hsa_circ_127197,RMVar_hsa_circ_222581,RMVar_hsa_circ_362739,RMVar_hsa_circ_368710,RMVar_hsa_circ_332746,RMVar_hsa_circ_80345,RMVar_hsa_circ_222582,RMVar_hsa_circ_222583,RMVar_hsa_circ_222590,RMVar_hsa_circ_269449,RMVar_hsa_circ_336219,RMVar_hsa_circ_375562,RMVar_hsa_circ_295734,RMVar_hsa_circ_94971,RMVar_hsa_circ_222588,RMVar_hsa_circ_222589,RMVar_hsa_circ_222587 24992 RMVar_ID_24992 Human_SNP_ID_162956204 A-to-I Human chr3 - 170131785 170131785 170131785 TTGCCCAGGCTGGAGTGCAATGGCACGATCCCAGATCACTGCAACTTCCGCCTCCCGAGTTCAAG TTGCCCAGGCTGGAGTGCAATGGCACGATCCCGGATCACTGCAACTTCCGCCTCCCGAGTTCAAG T C PHC3 Ensembl:ENSG00000173889 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs747264712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14719119,Human_RBP_ID_25713346 RMVar_hsa_circ_121381,RMVar_hsa_circ_112414,RMVar_hsa_circ_222554,RMVar_hsa_circ_369993,RMVar_hsa_circ_104786,RMVar_hsa_circ_84926,RMVar_hsa_circ_6537,RMVar_hsa_circ_222569,RMVar_hsa_circ_95793,RMVar_hsa_circ_222562,RMVar_hsa_circ_222563,RMVar_hsa_circ_222560,RMVar_hsa_circ_222561,RMVar_hsa_circ_101805,RMVar_hsa_circ_222567,RMVar_hsa_circ_222568,RMVar_hsa_circ_362889,RMVar_hsa_circ_82255,RMVar_hsa_circ_222577,RMVar_hsa_circ_323156,RMVar_hsa_circ_352667,RMVar_hsa_circ_312950,RMVar_hsa_circ_273803,RMVar_hsa_circ_222578,RMVar_hsa_circ_222576,RMVar_hsa_circ_127197,RMVar_hsa_circ_222581,RMVar_hsa_circ_362739,RMVar_hsa_circ_368710,RMVar_hsa_circ_332746,RMVar_hsa_circ_80345,RMVar_hsa_circ_222582,RMVar_hsa_circ_222583,RMVar_hsa_circ_222590,RMVar_hsa_circ_269449,RMVar_hsa_circ_336219,RMVar_hsa_circ_375562,RMVar_hsa_circ_295734,RMVar_hsa_circ_94971,RMVar_hsa_circ_222588,RMVar_hsa_circ_222589,RMVar_hsa_circ_222587 24993 RMVar_ID_24993 Human_SNP_ID_162959293 A-to-I Human chr3 - 170144083 170144083 170144083 ATCTCAGGTGATCTGCCCGCCTCAGCCTCCCAAAGTGCTGGGATTGCAGGCGTGAGCCACCACGC ATCTCAGGTGATCTGCCCGCCTCAGCCTCCCAGAGTGCTGGGATTGCAGGCGTGAGCCACCACGC T C PHC3 Ensembl:ENSG00000173889 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs918910266 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121381,RMVar_hsa_circ_112414,RMVar_hsa_circ_222554,RMVar_hsa_circ_369993,RMVar_hsa_circ_104786,RMVar_hsa_circ_222569,RMVar_hsa_circ_95793,RMVar_hsa_circ_222562,RMVar_hsa_circ_222560,RMVar_hsa_circ_222561,RMVar_hsa_circ_101805,RMVar_hsa_circ_222567,RMVar_hsa_circ_222568,RMVar_hsa_circ_362889,RMVar_hsa_circ_82255,RMVar_hsa_circ_222577,RMVar_hsa_circ_323156,RMVar_hsa_circ_352667,RMVar_hsa_circ_312950,RMVar_hsa_circ_222578,RMVar_hsa_circ_127197,RMVar_hsa_circ_222581,RMVar_hsa_circ_362739,RMVar_hsa_circ_368710,RMVar_hsa_circ_332746,RMVar_hsa_circ_80345,RMVar_hsa_circ_222592,RMVar_hsa_circ_104473,RMVar_hsa_circ_222582,RMVar_hsa_circ_222583,RMVar_hsa_circ_222590,RMVar_hsa_circ_336219,RMVar_hsa_circ_375562,RMVar_hsa_circ_295734,RMVar_hsa_circ_94971,RMVar_hsa_circ_222588,RMVar_hsa_circ_222589,RMVar_hsa_circ_222587,RMVar_hsa_circ_222596,RMVar_hsa_circ_270479,RMVar_hsa_circ_340200,RMVar_hsa_circ_222591,RMVar_hsa_circ_277745,RMVar_hsa_circ_272013,RMVar_hsa_circ_77849,RMVar_hsa_circ_83670,RMVar_hsa_circ_222597,RMVar_hsa_circ_222594,RMVar_hsa_circ_222595,RMVar_hsa_circ_222593 24994 RMVar_ID_24994 Human_SNP_ID_162959486 A-to-I Human chr3 - 170144865 170144860 170144866 CGGTCTTTACTAAAAATAAAAAAAATTGTTTAAGTGTGGTGCTGCGCTGCTGTAATTCCAGCTTT CGGTCTTTACTAAAAATAAAAAAAATTGTTT______GGTGCTGCGCTGCTGTAATTCCAGCTTT CACACTT C PHC3 Ensembl:ENSG00000173889 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs922643102 Functional Loss DEL dbSNP153 32..37 33 - - - Human_RBP_ID_7155048 RMVar_hsa_circ_121381,RMVar_hsa_circ_112414,RMVar_hsa_circ_222554,RMVar_hsa_circ_369993,RMVar_hsa_circ_104786,RMVar_hsa_circ_222569,RMVar_hsa_circ_95793,RMVar_hsa_circ_222562,RMVar_hsa_circ_222560,RMVar_hsa_circ_222561,RMVar_hsa_circ_101805,RMVar_hsa_circ_222567,RMVar_hsa_circ_222568,RMVar_hsa_circ_362889,RMVar_hsa_circ_82255,RMVar_hsa_circ_222577,RMVar_hsa_circ_323156,RMVar_hsa_circ_352667,RMVar_hsa_circ_312950,RMVar_hsa_circ_222578,RMVar_hsa_circ_127197,RMVar_hsa_circ_222581,RMVar_hsa_circ_362739,RMVar_hsa_circ_368710,RMVar_hsa_circ_332746,RMVar_hsa_circ_80345,RMVar_hsa_circ_222592,RMVar_hsa_circ_104473,RMVar_hsa_circ_222582,RMVar_hsa_circ_222583,RMVar_hsa_circ_222590,RMVar_hsa_circ_336219,RMVar_hsa_circ_375562,RMVar_hsa_circ_295734,RMVar_hsa_circ_94971,RMVar_hsa_circ_222588,RMVar_hsa_circ_222589,RMVar_hsa_circ_222587,RMVar_hsa_circ_222596,RMVar_hsa_circ_270479,RMVar_hsa_circ_340200,RMVar_hsa_circ_222591,RMVar_hsa_circ_277745,RMVar_hsa_circ_272013,RMVar_hsa_circ_77849,RMVar_hsa_circ_83670,RMVar_hsa_circ_222597,RMVar_hsa_circ_222594,RMVar_hsa_circ_222595,RMVar_hsa_circ_222593 24995 RMVar_ID_24995 Human_SNP_ID_162960101 A-to-I Human chr3 - 170146999 170146999 170146999 TCACGCTTGTAATCCCAGCTGCTCGGGAGGCTAATGCAGGAGAATCACTTGAACTCGGAAGGCAG TCACGCTTGTAATCCCAGCTGCTCGGGAGGCTGATGCAGGAGAATCACTTGAACTCGGAAGGCAG T C PHC3 Ensembl:ENSG00000173889 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1223974824 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14719549 RMVar_hsa_circ_121381,RMVar_hsa_circ_112414,RMVar_hsa_circ_222554,RMVar_hsa_circ_369993,RMVar_hsa_circ_104786,RMVar_hsa_circ_222562,RMVar_hsa_circ_222560,RMVar_hsa_circ_222561,RMVar_hsa_circ_101805,RMVar_hsa_circ_222568,RMVar_hsa_circ_362889,RMVar_hsa_circ_352667,RMVar_hsa_circ_312950,RMVar_hsa_circ_222578,RMVar_hsa_circ_127197,RMVar_hsa_circ_222581,RMVar_hsa_circ_368710,RMVar_hsa_circ_332746,RMVar_hsa_circ_80345,RMVar_hsa_circ_222592,RMVar_hsa_circ_104473,RMVar_hsa_circ_222582,RMVar_hsa_circ_222583,RMVar_hsa_circ_222590,RMVar_hsa_circ_336219,RMVar_hsa_circ_375562,RMVar_hsa_circ_94971,RMVar_hsa_circ_222588,RMVar_hsa_circ_222589,RMVar_hsa_circ_222596,RMVar_hsa_circ_270479,RMVar_hsa_circ_340200,RMVar_hsa_circ_222591,RMVar_hsa_circ_277745,RMVar_hsa_circ_77849,RMVar_hsa_circ_83670,RMVar_hsa_circ_222594,RMVar_hsa_circ_222595,RMVar_hsa_circ_222593,RMVar_hsa_circ_222602,RMVar_hsa_circ_116931,RMVar_hsa_circ_288412,RMVar_hsa_circ_303627,RMVar_hsa_circ_283172,RMVar_hsa_circ_124112,RMVar_hsa_circ_222604,RMVar_hsa_circ_86769,RMVar_hsa_circ_222603,RMVar_hsa_circ_222600,RMVar_hsa_circ_222601,RMVar_hsa_circ_222599 24996 RMVar_ID_24996 Human_SNP_ID_162961632 A-to-I Human chr3 - 170152723 170152723 170152723 CTAGGAAATTGGGGCTGCAGTGAGCCATGATCACTCCACTGCACCCCAGCCTGGGTGACAGAGGG CTAGGAAATTGGGGCTGCAGTGAGCCATGATCTCTCCACTGCACCCCAGCCTGGGTGACAGAGGG T A PHC3 Ensembl:ENSG00000173889 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs771599517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10079661,Human_RBP_ID_25768165 RMVar_hsa_circ_369993,RMVar_hsa_circ_104786,RMVar_hsa_circ_222560,RMVar_hsa_circ_222561,RMVar_hsa_circ_352667,RMVar_hsa_circ_368710,RMVar_hsa_circ_80345,RMVar_hsa_circ_222592,RMVar_hsa_circ_222582,RMVar_hsa_circ_222590,RMVar_hsa_circ_375562,RMVar_hsa_circ_94971,RMVar_hsa_circ_222589,RMVar_hsa_circ_270479,RMVar_hsa_circ_340200,RMVar_hsa_circ_77849,RMVar_hsa_circ_83670,RMVar_hsa_circ_222594,RMVar_hsa_circ_222595,RMVar_hsa_circ_222593,RMVar_hsa_circ_222602,RMVar_hsa_circ_116931,RMVar_hsa_circ_303627,RMVar_hsa_circ_283172,RMVar_hsa_circ_124112,RMVar_hsa_circ_86769,RMVar_hsa_circ_222603,RMVar_hsa_circ_222600,RMVar_hsa_circ_222601,RMVar_hsa_circ_222599,RMVar_hsa_circ_222608,RMVar_hsa_circ_303083,RMVar_hsa_circ_337873,RMVar_hsa_circ_222609 24997 RMVar_ID_24997 Human_SNP_ID_162964908 A-to-I Human chr3 - 170165668 170165667 170165669 CTCACTGCAACTTCCACCTCCTGGGTTCAAGCAGTTCTCATGCCTCACCCTCCCAAGTAGCTGGA CTCACTGCAACTTCCACCTCCTGGGTTCAAGTGATTCTCATGCCTCACCCTCCCAAGTAGCTGGA CTG TCA PHC3 Ensembl:ENSG00000173889 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs386668142 Functional Loss MNV dbSNP153 32..34 33 - - - RMVar_hsa_circ_369993,RMVar_hsa_circ_104786,RMVar_hsa_circ_222560,RMVar_hsa_circ_222561,RMVar_hsa_circ_352667,RMVar_hsa_circ_368710,RMVar_hsa_circ_80345,RMVar_hsa_circ_222592,RMVar_hsa_circ_222582,RMVar_hsa_circ_222590,RMVar_hsa_circ_375562,RMVar_hsa_circ_94971,RMVar_hsa_circ_222589,RMVar_hsa_circ_270479,RMVar_hsa_circ_340200,RMVar_hsa_circ_77849,RMVar_hsa_circ_83670,RMVar_hsa_circ_222594,RMVar_hsa_circ_222595,RMVar_hsa_circ_222593,RMVar_hsa_circ_222602,RMVar_hsa_circ_116931,RMVar_hsa_circ_303627,RMVar_hsa_circ_283172,RMVar_hsa_circ_124112,RMVar_hsa_circ_86769,RMVar_hsa_circ_222603,RMVar_hsa_circ_222600,RMVar_hsa_circ_222601,RMVar_hsa_circ_222599,RMVar_hsa_circ_222610,RMVar_hsa_circ_222608,RMVar_hsa_circ_303083,RMVar_hsa_circ_337873,RMVar_hsa_circ_222609 24998 RMVar_ID_24998 Human_SNP_ID_162964910 A-to-I Human chr3 - 170165668 170165668 170165668 CTCACTGCAACTTCCACCTCCTGGGTTCAAGCAGTTCTCATGCCTCACCCTCCCAAGTAGCTGGA CTCACTGCAACTTCCACCTCCTGGGTTCAAGCGGTTCTCATGCCTCACCCTCCCAAGTAGCTGGA T C PHC3 Ensembl:ENSG00000173889 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs570506743 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_369993,RMVar_hsa_circ_104786,RMVar_hsa_circ_222560,RMVar_hsa_circ_222561,RMVar_hsa_circ_352667,RMVar_hsa_circ_368710,RMVar_hsa_circ_80345,RMVar_hsa_circ_222592,RMVar_hsa_circ_222582,RMVar_hsa_circ_222590,RMVar_hsa_circ_375562,RMVar_hsa_circ_94971,RMVar_hsa_circ_222589,RMVar_hsa_circ_270479,RMVar_hsa_circ_340200,RMVar_hsa_circ_77849,RMVar_hsa_circ_83670,RMVar_hsa_circ_222594,RMVar_hsa_circ_222595,RMVar_hsa_circ_222593,RMVar_hsa_circ_222602,RMVar_hsa_circ_116931,RMVar_hsa_circ_303627,RMVar_hsa_circ_283172,RMVar_hsa_circ_124112,RMVar_hsa_circ_86769,RMVar_hsa_circ_222603,RMVar_hsa_circ_222600,RMVar_hsa_circ_222601,RMVar_hsa_circ_222599,RMVar_hsa_circ_222610,RMVar_hsa_circ_222608,RMVar_hsa_circ_303083,RMVar_hsa_circ_337873,RMVar_hsa_circ_222609 24999 RMVar_ID_24999 Human_SNP_ID_162965318 A-to-I Human chr3 - 170167277 170167277 170167277 GGATGTGGTGGCAAGCGCCTGTAGTTCCAGCTACTTAGGAGGCTGAGGTGGGAGGCTTGCTTGAG GGATGTGGTGGCAAGCGCCTGTAGTTCCAGCTGCTTAGGAGGCTGAGGTGGGAGGCTTGCTTGAG T C PHC3 Ensembl:ENSG00000173889 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1053703433 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_369993,RMVar_hsa_circ_104786,RMVar_hsa_circ_222560,RMVar_hsa_circ_222561,RMVar_hsa_circ_352667,RMVar_hsa_circ_368710,RMVar_hsa_circ_80345,RMVar_hsa_circ_222592,RMVar_hsa_circ_222582,RMVar_hsa_circ_222590,RMVar_hsa_circ_375562,RMVar_hsa_circ_94971,RMVar_hsa_circ_222589,RMVar_hsa_circ_270479,RMVar_hsa_circ_340200,RMVar_hsa_circ_77849,RMVar_hsa_circ_83670,RMVar_hsa_circ_222594,RMVar_hsa_circ_222595,RMVar_hsa_circ_222593,RMVar_hsa_circ_222602,RMVar_hsa_circ_116931,RMVar_hsa_circ_303627,RMVar_hsa_circ_283172,RMVar_hsa_circ_124112,RMVar_hsa_circ_86769,RMVar_hsa_circ_222603,RMVar_hsa_circ_222600,RMVar_hsa_circ_222601,RMVar_hsa_circ_222599,RMVar_hsa_circ_222610,RMVar_hsa_circ_222608,RMVar_hsa_circ_303083,RMVar_hsa_circ_337873,RMVar_hsa_circ_222609 25000 RMVar_ID_25000 Human_SNP_ID_162965520 A-to-I Human chr3 - 170168040 170168040 170168040 CTCCTACCTCAGACTGCTGAGTAGCTGGGACTACAGGCGCACACCACTATGCCTGGCTCATTTTT CTCCTACCTCAGACTGCTGAGTAGCTGGGACTGCAGGCGCACACCACTATGCCTGGCTCATTTTT T C PHC3 Ensembl:ENSG00000173889 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs979125590 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_369993,RMVar_hsa_circ_104786,RMVar_hsa_circ_222560,RMVar_hsa_circ_222561,RMVar_hsa_circ_352667,RMVar_hsa_circ_368710,RMVar_hsa_circ_80345,RMVar_hsa_circ_222592,RMVar_hsa_circ_222582,RMVar_hsa_circ_222590,RMVar_hsa_circ_375562,RMVar_hsa_circ_94971,RMVar_hsa_circ_222589,RMVar_hsa_circ_270479,RMVar_hsa_circ_340200,RMVar_hsa_circ_77849,RMVar_hsa_circ_83670,RMVar_hsa_circ_222594,RMVar_hsa_circ_222595,RMVar_hsa_circ_222593,RMVar_hsa_circ_222602,RMVar_hsa_circ_116931,RMVar_hsa_circ_303627,RMVar_hsa_circ_283172,RMVar_hsa_circ_124112,RMVar_hsa_circ_86769,RMVar_hsa_circ_222603,RMVar_hsa_circ_222600,RMVar_hsa_circ_222601,RMVar_hsa_circ_222599,RMVar_hsa_circ_222610,RMVar_hsa_circ_222608,RMVar_hsa_circ_303083,RMVar_hsa_circ_337873,RMVar_hsa_circ_222609 25001 RMVar_ID_25001 Human_SNP_ID_162965527 A-to-I Human chr3 - 170168086 170168086 170168086 ACGATCATAACTCACTACCGCCTCAATCTCCCAGGCTCAAGTGATCCTCCTACCTCAGACTGCTG ACGATCATAACTCACTACCGCCTCAATCTCCCGGGCTCAAGTGATCCTCCTACCTCAGACTGCTG T C PHC3 Ensembl:ENSG00000173889 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs896836154 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_369993,RMVar_hsa_circ_104786,RMVar_hsa_circ_222560,RMVar_hsa_circ_222561,RMVar_hsa_circ_352667,RMVar_hsa_circ_368710,RMVar_hsa_circ_80345,RMVar_hsa_circ_222592,RMVar_hsa_circ_222582,RMVar_hsa_circ_222590,RMVar_hsa_circ_375562,RMVar_hsa_circ_94971,RMVar_hsa_circ_222589,RMVar_hsa_circ_270479,RMVar_hsa_circ_340200,RMVar_hsa_circ_77849,RMVar_hsa_circ_83670,RMVar_hsa_circ_222594,RMVar_hsa_circ_222595,RMVar_hsa_circ_222593,RMVar_hsa_circ_222602,RMVar_hsa_circ_116931,RMVar_hsa_circ_303627,RMVar_hsa_circ_283172,RMVar_hsa_circ_124112,RMVar_hsa_circ_86769,RMVar_hsa_circ_222603,RMVar_hsa_circ_222600,RMVar_hsa_circ_222601,RMVar_hsa_circ_222599,RMVar_hsa_circ_222610,RMVar_hsa_circ_222608,RMVar_hsa_circ_303083,RMVar_hsa_circ_337873,RMVar_hsa_circ_222609 25002 RMVar_ID_25002 Human_SNP_ID_162984333 A-to-I Human chr3 + 170238825 170238825 170238825 TGTTGGCCAGGCTGGTCTTGAACTCTGGCCTCAAGTGATCCACCCGCCTTGGCCTCCCAAAGTGC TGTTGGCCAGGCTGGTCTTGAACTCTGGCCTCGAGTGATCCACCCGCCTTGGCCTCCCAAAGTGC A G PRKCI Ensembl:ENSG00000163558 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1189155540 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104002,RMVar_hsa_circ_362249,RMVar_hsa_circ_363151,RMVar_hsa_circ_353781,RMVar_hsa_circ_222613,RMVar_hsa_circ_44130,RMVar_hsa_circ_52574,RMVar_hsa_circ_222614 25003 RMVar_ID_25003 Human_SNP_ID_162985152 A-to-I Human chr3 + 170242133 170242133 170242133 CTCCGTCTCAAAAAAATTTTTTTTGTAGAGACAGGGTCTTGTTACATTGTTGCCCAGGCTGGTCT CTCCGTCTCAAAAAAATTTTTTTTGTAGAGACGGGGTCTTGTTACATTGTTGCCCAGGCTGGTCT A G PRKCI Ensembl:ENSG00000163558 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971717468 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104002,RMVar_hsa_circ_362249,RMVar_hsa_circ_363151,RMVar_hsa_circ_353781,RMVar_hsa_circ_222613,RMVar_hsa_circ_44130,RMVar_hsa_circ_52574,RMVar_hsa_circ_222614 25004 RMVar_ID_25004 Human_SNP_ID_162985153 A-to-I Human chr3 + 170242133 170242133 170242133 CTCCGTCTCAAAAAAATTTTTTTTGTAGAGACAGGGTCTTGTTACATTGTTGCCCAGGCTGGTCT CTCCGTCTCAAAAAAATTTTTTTTGTAGAGACTGGGTCTTGTTACATTGTTGCCCAGGCTGGTCT A T PRKCI Ensembl:ENSG00000163558 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971717468 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104002,RMVar_hsa_circ_362249,RMVar_hsa_circ_363151,RMVar_hsa_circ_353781,RMVar_hsa_circ_222613,RMVar_hsa_circ_44130,RMVar_hsa_circ_52574,RMVar_hsa_circ_222614 25005 RMVar_ID_25005 Human_SNP_ID_162986552 A-to-I Human chr3 + 170247636 170247636 170247636 CCTGCAATCCCAACTATTTGGGAGGCTGAGGCAGAAGAATCACTTGAACCTGGGAGGTGGAGGTT CCTGCAATCCCAACTATTTGGGAGGCTGAGGCGGAAGAATCACTTGAACCTGGGAGGTGGAGGTT A G PRKCI Ensembl:ENSG00000163558 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs538863728 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104002,RMVar_hsa_circ_362249,RMVar_hsa_circ_363151,RMVar_hsa_circ_353781,RMVar_hsa_circ_222613,RMVar_hsa_circ_44130,RMVar_hsa_circ_52574,RMVar_hsa_circ_222614 25006 RMVar_ID_25006 Human_SNP_ID_162993230 A-to-I Human chr3 + 170273553 170273553 170273553 AAGACAACTGTGGGCTGGGTGCGGTGGTTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGC AAGACAACTGTGGGCTGGGTGCGGTGGTTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGC A G PRKCI Ensembl:ENSG00000163558 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1310801030 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6487,RMVar_hsa_circ_104002,RMVar_hsa_circ_362249,RMVar_hsa_circ_363151,RMVar_hsa_circ_222613,RMVar_hsa_circ_44130,RMVar_hsa_circ_222614,RMVar_hsa_circ_265874,RMVar_hsa_circ_288678,RMVar_hsa_circ_342417,RMVar_hsa_circ_294367,RMVar_hsa_circ_37415,RMVar_hsa_circ_82044,RMVar_hsa_circ_11931,RMVar_hsa_circ_357871,RMVar_hsa_circ_222615,RMVar_hsa_circ_222616,RMVar_hsa_circ_375821,RMVar_hsa_circ_52745,RMVar_hsa_circ_70750,RMVar_hsa_circ_351673,RMVar_hsa_circ_359084,RMVar_hsa_circ_222618,RMVar_hsa_circ_356683,RMVar_hsa_circ_318961,RMVar_hsa_circ_327425,RMVar_hsa_circ_318297,RMVar_hsa_circ_109045,RMVar_hsa_circ_103964,RMVar_hsa_circ_222620,RMVar_hsa_circ_13540,RMVar_hsa_circ_48793,RMVar_hsa_circ_222621,RMVar_hsa_circ_222619 25007 RMVar_ID_25007 Human_SNP_ID_162994125 A-to-I Human chr3 + 170277126 170277126 170277126 AAAAAAAAATTAGGGCGTGGTGGCACACACCTATAATACTAGCTACTTAAGAGGTTGAGGCACGA AAAAAAAAATTAGGGCGTGGTGGCACACACCTGTAATACTAGCTACTTAAGAGGTTGAGGCACGA A G PRKCI Ensembl:ENSG00000163558 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs888904900 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6487,RMVar_hsa_circ_104002,RMVar_hsa_circ_362249,RMVar_hsa_circ_363151,RMVar_hsa_circ_222613,RMVar_hsa_circ_44130,RMVar_hsa_circ_222614,RMVar_hsa_circ_265874,RMVar_hsa_circ_288678,RMVar_hsa_circ_342417,RMVar_hsa_circ_37415,RMVar_hsa_circ_82044,RMVar_hsa_circ_11931,RMVar_hsa_circ_357871,RMVar_hsa_circ_222615,RMVar_hsa_circ_222616,RMVar_hsa_circ_375821,RMVar_hsa_circ_52745,RMVar_hsa_circ_70750,RMVar_hsa_circ_351673,RMVar_hsa_circ_359084,RMVar_hsa_circ_222618,RMVar_hsa_circ_356683,RMVar_hsa_circ_318961,RMVar_hsa_circ_318297,RMVar_hsa_circ_109045,RMVar_hsa_circ_103964,RMVar_hsa_circ_222620,RMVar_hsa_circ_13540,RMVar_hsa_circ_48793,RMVar_hsa_circ_222621,RMVar_hsa_circ_378952,RMVar_hsa_circ_222619 25008 RMVar_ID_25008 Human_SNP_ID_162996992 A-to-I Human chr3 + 170288066 170288066 170288066 AGGAGATTGAGACCATCCTGGCTAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAAAATT AGGAGATTGAGACCATCCTGGCTAACATGGTGGAACCCCGTCTCTACTAAAAATACAAAAAAATT A G PRKCI Ensembl:ENSG00000163558 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1218246725 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104002,RMVar_hsa_circ_222614,RMVar_hsa_circ_265874,RMVar_hsa_circ_342417,RMVar_hsa_circ_37415,RMVar_hsa_circ_17425,RMVar_hsa_circ_82044,RMVar_hsa_circ_11931,RMVar_hsa_circ_357871,RMVar_hsa_circ_351673,RMVar_hsa_circ_359084,RMVar_hsa_circ_356683,RMVar_hsa_circ_109045,RMVar_hsa_circ_103964,RMVar_hsa_circ_222620,RMVar_hsa_circ_222621,RMVar_hsa_circ_12519,RMVar_hsa_circ_322181,RMVar_hsa_circ_222619,RMVar_hsa_circ_342728,RMVar_hsa_circ_222623,RMVar_hsa_circ_99568,RMVar_hsa_circ_315903,RMVar_hsa_circ_222624,RMVar_hsa_circ_374086,RMVar_hsa_circ_343189,RMVar_hsa_circ_303458,RMVar_hsa_circ_222625 25009 RMVar_ID_25009 Human_SNP_ID_162997016 A-to-I Human chr3 + 170288135 170288135 170288135 AGGCGTGGTGGCGGACGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCGAGAA AGGCGTGGTGGCGGACGCCTGTAGTCCCAGCTGCTCGGGAGGCTGAGGCAGGAGAATGGCGAGAA A G PRKCI Ensembl:ENSG00000163558 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1237597994 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104002,RMVar_hsa_circ_222614,RMVar_hsa_circ_265874,RMVar_hsa_circ_342417,RMVar_hsa_circ_37415,RMVar_hsa_circ_17425,RMVar_hsa_circ_82044,RMVar_hsa_circ_11931,RMVar_hsa_circ_357871,RMVar_hsa_circ_351673,RMVar_hsa_circ_359084,RMVar_hsa_circ_356683,RMVar_hsa_circ_109045,RMVar_hsa_circ_103964,RMVar_hsa_circ_222620,RMVar_hsa_circ_222621,RMVar_hsa_circ_12519,RMVar_hsa_circ_322181,RMVar_hsa_circ_222619,RMVar_hsa_circ_342728,RMVar_hsa_circ_222623,RMVar_hsa_circ_99568,RMVar_hsa_circ_315903,RMVar_hsa_circ_222624,RMVar_hsa_circ_374086,RMVar_hsa_circ_343189,RMVar_hsa_circ_303458,RMVar_hsa_circ_222625 25010 RMVar_ID_25010 Human_SNP_ID_163000004 A-to-I Human chr3 + 170299774 170299774 170299774 GAGTCAGGATTCAAACCCAAATCTGACTGACTAAGGCCTGTGCTCTTTCTACCACGCTGCACTGT GAGTCAGGATTCAAACCCAAATCTGACTGACTGAGGCCTGTGCTCTTTCTACCACGCTGCACTGT A G PRKCI Ensembl:ENSG00000163558 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs114394848 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14721059 RMVar_hsa_circ_265874,RMVar_hsa_circ_222623,RMVar_hsa_circ_99568,RMVar_hsa_circ_104406,RMVar_hsa_circ_222628,RMVar_hsa_circ_86370,RMVar_hsa_circ_222634,RMVar_hsa_circ_222635,RMVar_hsa_circ_107264 25011 RMVar_ID_25011 Human_SNP_ID_163000854 A-to-I Human chr3 + 170303772 170303772 170303772 TGATCCCAGTACTTTGGGAGGTTGAGGCGGGCAGATCACTTGAGGTCAGGAGTTTGAGATTGGCC TGATCCCAGTACTTTGGGAGGTTGAGGCGGGCGGATCACTTGAGGTCAGGAGTTTGAGATTGGCC A G PRKCI Ensembl:ENSG00000163558 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991528486 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265874,RMVar_hsa_circ_222623,RMVar_hsa_circ_99568,RMVar_hsa_circ_104406,RMVar_hsa_circ_222628,RMVar_hsa_circ_86370,RMVar_hsa_circ_222634,RMVar_hsa_circ_222635,RMVar_hsa_circ_107264 25012 RMVar_ID_25012 Human_SNP_ID_163016371 A-to-I Human chr3 + 170362628 170362628 170362628 CTTCAGGTCAGGAGTTTGAGACCAGCCTGGCCAACATGGTAAAACCCCATCTCTACTAAAAATAC CTTCAGGTCAGGAGTTTGAGACCAGCCTGGCCGACATGGTAAAACCCCATCTCTACTAAAAATAC A G SKIL Ensembl:ENSG00000136603 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1560206271 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_222637,RMVar_hsa_circ_276490,RMVar_hsa_circ_294380,RMVar_hsa_circ_297385,RMVar_hsa_circ_271475,RMVar_hsa_circ_222639,RMVar_hsa_circ_222638,RMVar_hsa_circ_68507,RMVar_hsa_circ_222641,RMVar_hsa_circ_222636,RMVar_hsa_circ_298504 25013 RMVar_ID_25013 Human_SNP_ID_163017383 A-to-I Human chr3 + 170365953 170365953 170365953 AATTTTTTTATTTTTAGTCCAGACGGGGTTTCACCATGCTGGCCAGGCTGATCTTGAACTCCTGA AATTTTTTTATTTTTAGTCCAGACGGGGTTTCGCCATGCTGGCCAGGCTGATCTTGAACTCCTGA A G SKIL Ensembl:ENSG00000136603 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs937237978 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_222637,RMVar_hsa_circ_276490,RMVar_hsa_circ_294380,RMVar_hsa_circ_297385,RMVar_hsa_circ_271475,RMVar_hsa_circ_222639,RMVar_hsa_circ_222638,RMVar_hsa_circ_68507,RMVar_hsa_circ_222641,RMVar_hsa_circ_222636,RMVar_hsa_circ_298504 25014 RMVar_ID_25014 Human_SNP_ID_163017384 A-to-I Human chr3 + 170365953 170365953 170365953 AATTTTTTTATTTTTAGTCCAGACGGGGTTTCACCATGCTGGCCAGGCTGATCTTGAACTCCTGA AATTTTTTTATTTTTAGTCCAGACGGGGTTTCTCCATGCTGGCCAGGCTGATCTTGAACTCCTGA A T SKIL Ensembl:ENSG00000136603 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs937237978 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_222637,RMVar_hsa_circ_276490,RMVar_hsa_circ_294380,RMVar_hsa_circ_297385,RMVar_hsa_circ_271475,RMVar_hsa_circ_222639,RMVar_hsa_circ_222638,RMVar_hsa_circ_68507,RMVar_hsa_circ_222641,RMVar_hsa_circ_222636,RMVar_hsa_circ_298504 25015 RMVar_ID_25015 Human_SNP_ID_163018508 A-to-I Human chr3 + 170369422 170369422 170369422 TAATCAAGAATTGGGCTAATTTTTTTTTTGATAAGGAGTTTTGCTCTTGTAGCTCAGGCTGGAGT TAATCAAGAATTGGGCTAATTTTTTTTTTGATGAGGAGTTTTGCTCTTGTAGCTCAGGCTGGAGT A G SKIL Ensembl:ENSG00000136603 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917428052 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14721341 RMVar_hsa_circ_222637,RMVar_hsa_circ_276490,RMVar_hsa_circ_294380,RMVar_hsa_circ_297385,RMVar_hsa_circ_271475,RMVar_hsa_circ_222639,RMVar_hsa_circ_222638,RMVar_hsa_circ_68507,RMVar_hsa_circ_222641,RMVar_hsa_circ_222636,RMVar_hsa_circ_298504 25016 RMVar_ID_25016 Human_SNP_ID_163021833 A-to-I Human chr3 + 170380850 170380850 170380850 TTATTGGAAGATGACTCTTGAGACAGGGTCTCACTCTTGCCCAGGATAGAGTGCAGTGGTGCAAT TTATTGGAAGATGACTCTTGAGACAGGGTCTCTCTCTTGCCCAGGATAGAGTGCAGTGGTGCAAT A T SKIL Ensembl:ENSG00000136603 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1473603908 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_222637,RMVar_hsa_circ_276490,RMVar_hsa_circ_294380,RMVar_hsa_circ_297385,RMVar_hsa_circ_271475,RMVar_hsa_circ_222639,RMVar_hsa_circ_222638,RMVar_hsa_circ_68507,RMVar_hsa_circ_222641,RMVar_hsa_circ_222636,RMVar_hsa_circ_298504 25017 RMVar_ID_25017 Human_SNP_ID_163035736 A-to-I Human chr3 + 170435001 170435001 170435001 TGCCACCACACCTGGCTAATTTTTGTATTTTTAGTGGAGACAGGGTTTTGCCATGTTGGCCGGGG TGCCACCACACCTGGCTAATTTTTGTATTTTTGGTGGAGACAGGGTTTTGCCATGTTGGCCGGGG A G CLDN11,AC026316.4 Ensembl:ENSG00000013297,Ensembl:ENSG00000285218 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs533590522 Functional Loss SNV dbSNP153 33..33 33 - - - 25018 RMVar_ID_25018 Human_SNP_ID_163042378 A-to-I Human chr3 - 170463620 170463620 170463620 CCAGATAGTTGAGAGACTGAGGGAGGAGGATCACTTGAGCCCAGGAGTTCAAGGCTGCAGTGAGC CCAGATAGTTGAGAGACTGAGGGAGGAGGATCGCTTGAGCCCAGGAGTTCAAGGCTGCAGTGAGC T C SLC7A14 Ensembl:ENSG00000013293 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs924754920 Functional Loss SNV dbSNP153 33..33 33 - - - 25019 RMVar_ID_25019 Human_SNP_ID_163146353 A-to-I Human chr3 - 170900152 170900152 170900152 TGGCCAGGTTGGTCTCGGACTCCTGACCTCAAATGATCCGCCTGCCTTGGCCTCCCGAAGTGCTA TGGCCAGGTTGGTCTCGGACTCCTGACCTCAAGTGATCCGCCTGCCTTGGCCTCCCGAAGTGCTA T C EIF5A2 Ensembl:ENSG00000163577 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1560010237 Functional Loss SNV dbSNP153 33..33 33 - - - 25020 RMVar_ID_25020 Human_SNP_ID_163328007 A-to-I Human chr3 - 171654083 171654082 171654084 TCGGCCAGGCTAGCTTTGAACTCCTAACCTCAAGTGATCCGCCCACCTCGGCCTCCCAAAGTGCC TCGGCCAGGCTAGCTTTGAACTCCTAACCTC__GTGATCCGCCCACCTCGGCCTCCCAAAGTGCC CTT C PLD1 Ensembl:ENSG00000075651 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1207110183 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_21289,RMVar_hsa_circ_337669,RMVar_hsa_circ_77084,RMVar_hsa_circ_222681,RMVar_hsa_circ_360374,RMVar_hsa_circ_70312,RMVar_hsa_circ_325785,RMVar_hsa_circ_35010,RMVar_hsa_circ_59973,RMVar_hsa_circ_222684,RMVar_hsa_circ_222682,RMVar_hsa_circ_222683,RMVar_hsa_circ_316424,RMVar_hsa_circ_367565,RMVar_hsa_circ_325111,RMVar_hsa_circ_32293,RMVar_hsa_circ_326475,RMVar_hsa_circ_355961,RMVar_hsa_circ_362081,RMVar_hsa_circ_371241,RMVar_hsa_circ_349978,RMVar_hsa_circ_293635,RMVar_hsa_circ_222686,RMVar_hsa_circ_222687,RMVar_hsa_circ_222685 25021 RMVar_ID_25021 Human_SNP_ID_163328013 A-to-I Human chr3 - 171654104 171654104 171654104 TGGAGACGGGGTTTCACCATGTCGGCCAGGCTAGCTTTGAACTCCTAACCTCAAGTGATCCGCCC TGGAGACGGGGTTTCACCATGTCGGCCAGGCTGGCTTTGAACTCCTAACCTCAAGTGATCCGCCC T C PLD1 Ensembl:ENSG00000075651 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1360558494 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21289,RMVar_hsa_circ_337669,RMVar_hsa_circ_77084,RMVar_hsa_circ_222681,RMVar_hsa_circ_360374,RMVar_hsa_circ_70312,RMVar_hsa_circ_325785,RMVar_hsa_circ_35010,RMVar_hsa_circ_59973,RMVar_hsa_circ_222684,RMVar_hsa_circ_222682,RMVar_hsa_circ_222683,RMVar_hsa_circ_316424,RMVar_hsa_circ_367565,RMVar_hsa_circ_325111,RMVar_hsa_circ_32293,RMVar_hsa_circ_326475,RMVar_hsa_circ_355961,RMVar_hsa_circ_362081,RMVar_hsa_circ_371241,RMVar_hsa_circ_349978,RMVar_hsa_circ_293635,RMVar_hsa_circ_222686,RMVar_hsa_circ_222687,RMVar_hsa_circ_222685 25022 RMVar_ID_25022 Human_SNP_ID_163333025 A-to-I Human chr3 - 171676123 171676123 171676123 GTACGTATCATTCAGGCCAGGCACGGTGGCCCACGACTGTAATCCTGGCACTTTGGGAGGCCTAG GTACGTATCATTCAGGCCAGGCACGGTGGCCCGCGACTGTAATCCTGGCACTTTGGGAGGCCTAG T C PLD1 Ensembl:ENSG00000075651 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1365127750 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21289,RMVar_hsa_circ_337669,RMVar_hsa_circ_360374,RMVar_hsa_circ_70312,RMVar_hsa_circ_325785,RMVar_hsa_circ_35010,RMVar_hsa_circ_59973,RMVar_hsa_circ_222684,RMVar_hsa_circ_222682,RMVar_hsa_circ_222683,RMVar_hsa_circ_367565,RMVar_hsa_circ_325111,RMVar_hsa_circ_32293,RMVar_hsa_circ_326475,RMVar_hsa_circ_371241,RMVar_hsa_circ_349978,RMVar_hsa_circ_293635,RMVar_hsa_circ_73606,RMVar_hsa_circ_222686,RMVar_hsa_circ_222687,RMVar_hsa_circ_363153,RMVar_hsa_circ_222685,RMVar_hsa_circ_362347,RMVar_hsa_circ_345277,RMVar_hsa_circ_27571,RMVar_hsa_circ_65709,RMVar_hsa_circ_24312,RMVar_hsa_circ_351350,RMVar_hsa_circ_356694,RMVar_hsa_circ_368461,RMVar_hsa_circ_58780,RMVar_hsa_circ_283353,RMVar_hsa_circ_222690,RMVar_hsa_circ_30988,RMVar_hsa_circ_222689 25023 RMVar_ID_25023 Human_SNP_ID_163423861 A-to-I Human chr3 + 172053752 172053752 172053752 CGAGACTGCGCCATTGCCCTGCACTCCAGCCTAGGTGACAGGGCGAAACTCCGTCTCAAAAAAAA CGAGACTGCGCCATTGCCCTGCACTCCAGCCTGGGTGACAGGGCGAAACTCCGTCTCAAAAAAAA A G FNDC3B Ensembl:ENSG00000075420 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1446306337 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77864,RMVar_hsa_circ_119173,RMVar_hsa_circ_100721,RMVar_hsa_circ_222704,RMVar_hsa_circ_115632,RMVar_hsa_circ_222700,RMVar_hsa_circ_222701,RMVar_hsa_circ_222702,RMVar_hsa_circ_123167,RMVar_hsa_circ_85623,RMVar_hsa_circ_101084,RMVar_hsa_circ_222705,RMVar_hsa_circ_222706,RMVar_hsa_circ_222703 25024 RMVar_ID_25024 Human_SNP_ID_163444854 A-to-I Human chr3 + 172145864 172145848 172145865 AGATGGAGTTTCACTCTTGTTGCCCAGGCTGGAGTGCAATGGTGTGATCTCGGCTCACTGCAACC AGATGGAGTTTCACTCT_________________TGCAATGGTGTGATCTCGGCTCACTGCAACC TTGTTGCCCAGGCTGGAG T FNDC3B Ensembl:ENSG00000075420 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1433687519 Functional Loss DEL dbSNP153 18..34 33 - - - RMVar_hsa_circ_116748,RMVar_hsa_circ_119173,RMVar_hsa_circ_222704,RMVar_hsa_circ_115632,RMVar_hsa_circ_222702,RMVar_hsa_circ_85623,RMVar_hsa_circ_101084,RMVar_hsa_circ_222705,RMVar_hsa_circ_275337,RMVar_hsa_circ_307068,RMVar_hsa_circ_222703,RMVar_hsa_circ_347140,RMVar_hsa_circ_367705,RMVar_hsa_circ_330185,RMVar_hsa_circ_302361,RMVar_hsa_circ_125387,RMVar_hsa_circ_272725,RMVar_hsa_circ_121390,RMVar_hsa_circ_222712,RMVar_hsa_circ_74080,RMVar_hsa_circ_89823,RMVar_hsa_circ_106552,RMVar_hsa_circ_82508,RMVar_hsa_circ_222714,RMVar_hsa_circ_222716,RMVar_hsa_circ_222715,RMVar_hsa_circ_222713,RMVar_hsa_circ_222721,RMVar_hsa_circ_222708,RMVar_hsa_circ_222710,RMVar_hsa_circ_222711,RMVar_hsa_circ_222709,RMVar_hsa_circ_334782,RMVar_hsa_circ_347653,RMVar_hsa_circ_102806,RMVar_hsa_circ_65676,RMVar_hsa_circ_222719,RMVar_hsa_circ_222720 25025 RMVar_ID_25025 Human_SNP_ID_163444858 A-to-I Human chr3 + 172145864 172145864 172145864 AGATGGAGTTTCACTCTTGTTGCCCAGGCTGGAGTGCAATGGTGTGATCTCGGCTCACTGCAACC AGATGGAGTTTCACTCTTGTTGCCCAGGCTGGCGTGCAATGGTGTGATCTCGGCTCACTGCAACC A C FNDC3B Ensembl:ENSG00000075420 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs988608518 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116748,RMVar_hsa_circ_119173,RMVar_hsa_circ_222704,RMVar_hsa_circ_115632,RMVar_hsa_circ_222702,RMVar_hsa_circ_85623,RMVar_hsa_circ_101084,RMVar_hsa_circ_222705,RMVar_hsa_circ_275337,RMVar_hsa_circ_307068,RMVar_hsa_circ_222703,RMVar_hsa_circ_347140,RMVar_hsa_circ_367705,RMVar_hsa_circ_330185,RMVar_hsa_circ_302361,RMVar_hsa_circ_125387,RMVar_hsa_circ_272725,RMVar_hsa_circ_121390,RMVar_hsa_circ_222712,RMVar_hsa_circ_74080,RMVar_hsa_circ_89823,RMVar_hsa_circ_106552,RMVar_hsa_circ_82508,RMVar_hsa_circ_222714,RMVar_hsa_circ_222716,RMVar_hsa_circ_222715,RMVar_hsa_circ_222713,RMVar_hsa_circ_222721,RMVar_hsa_circ_222708,RMVar_hsa_circ_222710,RMVar_hsa_circ_222711,RMVar_hsa_circ_222709,RMVar_hsa_circ_334782,RMVar_hsa_circ_347653,RMVar_hsa_circ_102806,RMVar_hsa_circ_65676,RMVar_hsa_circ_222719,RMVar_hsa_circ_222720 25026 RMVar_ID_25026 Human_SNP_ID_163485138 A-to-I Human chr3 + 172315266 172315266 172315266 GGGCATGACAGTGGGCGCCTATAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATTGCTAGAA GGGCATGACAGTGGGCGCCTATAGTCCCAGCTCCTTGGGAGGCTGAGGCAGGAGAATTGCTAGAA A C FNDC3B Ensembl:ENSG00000075420 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs921583132 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_347140,RMVar_hsa_circ_125387,RMVar_hsa_circ_121390,RMVar_hsa_circ_222712,RMVar_hsa_circ_74080,RMVar_hsa_circ_89823,RMVar_hsa_circ_106552,RMVar_hsa_circ_82508,RMVar_hsa_circ_222713,RMVar_hsa_circ_222708,RMVar_hsa_circ_222710,RMVar_hsa_circ_222711,RMVar_hsa_circ_222709,RMVar_hsa_circ_102806,RMVar_hsa_circ_222719,RMVar_hsa_circ_368020,RMVar_hsa_circ_353385,RMVar_hsa_circ_80685,RMVar_hsa_circ_86500,RMVar_hsa_circ_222729,RMVar_hsa_circ_375230,RMVar_hsa_circ_359698,RMVar_hsa_circ_123781,RMVar_hsa_circ_97276,RMVar_hsa_circ_222740,RMVar_hsa_circ_59032,RMVar_hsa_circ_68173,RMVar_hsa_circ_222742,RMVar_hsa_circ_222743,RMVar_hsa_circ_222744,RMVar_hsa_circ_222741,RMVar_hsa_circ_70224,RMVar_hsa_circ_368611,RMVar_hsa_circ_69990,RMVar_hsa_circ_92831,RMVar_hsa_circ_83778,RMVar_hsa_circ_222749,RMVar_hsa_circ_276538,RMVar_hsa_circ_358999,RMVar_hsa_circ_371004,RMVar_hsa_circ_121851,RMVar_hsa_circ_76753,RMVar_hsa_circ_60788,RMVar_hsa_circ_222752,RMVar_hsa_circ_222753,RMVar_hsa_circ_222754,RMVar_hsa_circ_222751 25027 RMVar_ID_25027 Human_SNP_ID_163485139 A-to-I Human chr3 + 172315266 172315266 172315266 GGGCATGACAGTGGGCGCCTATAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATTGCTAGAA GGGCATGACAGTGGGCGCCTATAGTCCCAGCTGCTTGGGAGGCTGAGGCAGGAGAATTGCTAGAA A G FNDC3B Ensembl:ENSG00000075420 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs921583132 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_347140,RMVar_hsa_circ_125387,RMVar_hsa_circ_121390,RMVar_hsa_circ_222712,RMVar_hsa_circ_74080,RMVar_hsa_circ_89823,RMVar_hsa_circ_106552,RMVar_hsa_circ_82508,RMVar_hsa_circ_222713,RMVar_hsa_circ_222708,RMVar_hsa_circ_222710,RMVar_hsa_circ_222711,RMVar_hsa_circ_222709,RMVar_hsa_circ_102806,RMVar_hsa_circ_222719,RMVar_hsa_circ_368020,RMVar_hsa_circ_353385,RMVar_hsa_circ_80685,RMVar_hsa_circ_86500,RMVar_hsa_circ_222729,RMVar_hsa_circ_375230,RMVar_hsa_circ_359698,RMVar_hsa_circ_123781,RMVar_hsa_circ_97276,RMVar_hsa_circ_222740,RMVar_hsa_circ_59032,RMVar_hsa_circ_68173,RMVar_hsa_circ_222742,RMVar_hsa_circ_222743,RMVar_hsa_circ_222744,RMVar_hsa_circ_222741,RMVar_hsa_circ_70224,RMVar_hsa_circ_368611,RMVar_hsa_circ_69990,RMVar_hsa_circ_92831,RMVar_hsa_circ_83778,RMVar_hsa_circ_222749,RMVar_hsa_circ_276538,RMVar_hsa_circ_358999,RMVar_hsa_circ_371004,RMVar_hsa_circ_121851,RMVar_hsa_circ_76753,RMVar_hsa_circ_60788,RMVar_hsa_circ_222752,RMVar_hsa_circ_222753,RMVar_hsa_circ_222754,RMVar_hsa_circ_222751 25028 RMVar_ID_25028 Human_SNP_ID_163505676 A-to-I Human chr3 + 172400513 172400513 172400513 TGGACATACATTCCAAGCTTTTCAACTCTAGGAGAAAAAGAAAATCATGTTTTCCTGTATTGTAA TGGACATACATTCCAAGCTTTTCAACTCTAGGGGAAAAAGAAAATCATGTTTTCCTGTATTGTAA A G FNDC3B Ensembl:ENSG00000075420 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs906824234 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7157723,Human_RBP_ID_8565378 RMVar_hsa_circ_121390,RMVar_hsa_circ_222708,RMVar_hsa_circ_86500,RMVar_hsa_circ_222729,RMVar_hsa_circ_92957,RMVar_hsa_circ_222759 25029 RMVar_ID_25029 Human_SNP_ID_163580290 A-to-I Human chr3 - 172694032 172694032 172694032 AAAGTTGGCTGGGTGTGGTGGCACGTGCCTATAGTCCTAGCTACTCAGGAGGCTGAGGTGGGAGG AAAGTTGGCTGGGTGTGGTGGCACGTGCCTATGGTCCTAGCTACTCAGGAGGCTGAGGTGGGAGG T C NCEH1 Ensembl:ENSG00000144959 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1311453176 Functional Loss SNV dbSNP153 33..33 33 - - - 25030 RMVar_ID_25030 Human_SNP_ID_163581884 A-to-I Human chr3 - 172700570 172700570 172700570 CTAGGAGGTGAAGGCTGTATGATCACACCACTACACTCTAGCCTGGGTGACAGAGCAAGACCCTG CTAGGAGGTGAAGGCTGTATGATCACACCACTGCACTCTAGCCTGGGTGACAGAGCAAGACCCTG T C NCEH1 Ensembl:ENSG00000144959 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1320843985 Functional Loss SNV dbSNP153 33..33 33 - - - 25031 RMVar_ID_25031 Human_SNP_ID_163604241 A-to-I Human chr3 + 172789376 172789376 172789376 CAGATGTGCACCACCACACCTGGCTAACTTTTATATTTTCTGTAGAGATGGGGTTTTGCCATGTA CAGATGTGCACCACCACACCTGGCTAACTTTTGTATTTTCTGTAGAGATGGGGTTTTGCCATGTA A G ECT2 Ensembl:ENSG00000114346 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569920593 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7010,RMVar_hsa_circ_95318,RMVar_hsa_circ_65827,RMVar_hsa_circ_222768,RMVar_hsa_circ_80247,RMVar_hsa_circ_222775,RMVar_hsa_circ_109629,RMVar_hsa_circ_222776,RMVar_hsa_circ_17895,RMVar_hsa_circ_22090,RMVar_hsa_circ_31099,RMVar_hsa_circ_65802,RMVar_hsa_circ_94374,RMVar_hsa_circ_222783,RMVar_hsa_circ_222784,RMVar_hsa_circ_50077,RMVar_hsa_circ_274783,RMVar_hsa_circ_374526,RMVar_hsa_circ_222786,RMVar_hsa_circ_222787 25032 RMVar_ID_25032 Human_SNP_ID_163607684 A-to-I Human chr3 + 172803944 172803944 172803944 TTCTTATCCCAACATCGCAAGTAGCTGAGACTATAGACACTCGCCACCACACCAGTCTAATTATT TTCTTATCCCAACATCGCAAGTAGCTGAGACTGTAGACACTCGCCACCACACCAGTCTAATTATT A G ECT2 Ensembl:ENSG00000114346 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909386802 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14727439,Human_RBP_ID_20858470 RMVar_hsa_circ_7010,RMVar_hsa_circ_80247,RMVar_hsa_circ_222775,RMVar_hsa_circ_109629,RMVar_hsa_circ_222776,RMVar_hsa_circ_17895,RMVar_hsa_circ_65802,RMVar_hsa_circ_94374,RMVar_hsa_circ_222783,RMVar_hsa_circ_222784,RMVar_hsa_circ_274783,RMVar_hsa_circ_374526,RMVar_hsa_circ_70719,RMVar_hsa_circ_222786,RMVar_hsa_circ_222787,RMVar_hsa_circ_344022,RMVar_hsa_circ_61910 25033 RMVar_ID_25033 Human_SNP_ID_163678052 A-to-I Human chr3 - 173117121 173117121 173117121 CTTGGCAGCAGGACAGTTCAGAACAGCACTTGAGGTATGGGATTAAAGAAAATATAGATTGGTGA CTTGGCAGCAGGACAGTTCAGAACAGCACTTGGGGTATGGGATTAAAGAAAATATAGATTGGTGA T C SPATA16 Ensembl:ENSG00000144962 Protein coding CDS GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs768914085 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_507765 25034 RMVar_ID_25034 Human_SNP_ID_163678054 A-to-I Human chr3 - 173117126 173117126 173117126 TACGCCTTGGCAGCAGGACAGTTCAGAACAGCACTTGAGGTATGGGATTAAAGAAAATATAGATT TACGCCTTGGCAGCAGGACAGTTCAGAACAGCGCTTGAGGTATGGGATTAAAGAAAATATAGATT T C SPATA16 Ensembl:ENSG00000144962 Protein coding CDS GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs912575351 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_507765 25035 RMVar_ID_25035 Human_SNP_ID_163763012 A-to-I Human chr3 + 173484795 173484795 173484795 AGATGGACATACCCTTTGATCTGTTCATTTATATGACTCAAAGGAACAGTGATAGTGATAGAGGA AGATGGACATACCCTTTGATCTGTTCATTTATGTGACTCAAAGGAACAGTGATAGTGATAGAGGA A G NLGN1 Ensembl:ENSG00000169760 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs747330671 Functional Loss SNV dbSNP153 33..33 33 - - - 25036 RMVar_ID_25036 Human_SNP_ID_163850138 A-to-I Human chr3 + 173840443 173840442 173840443 GAATTGCTTAAAAGCATGTAAAAGTGGAGAGTAATCACTGTGAAGTTAGTAGTTTCTATGCTCAC GAATTGCTTAAAAGCATGTAAAAGTGGAGAGT_ATCACTGTGAAGTTAGTAGTTTCTATGCTCAC TA T NLGN1 Ensembl:ENSG00000169760 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1276906640 Functional Loss DEL dbSNP153 33..33 33 - - - 25037 RMVar_ID_25037 Human_SNP_ID_163850146 A-to-I Human chr3 + 173840458 173840456 173840459 ATGTAAAAGTGGAGAGTAATCACTGTGAAGTTAGTAGTTTCTATGCTCACAGTGTGAATTTGTCA ATGTAAAAGTGGAGAGTAATCACTGTGAAGT___TAGTTTCTATGCTCACAGTGTGAATTTGTCA TTAG T NLGN1 Ensembl:ENSG00000169760 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1441359989 Functional Loss DEL dbSNP153 32..34 33 - - - 25038 RMVar_ID_25038 Human_SNP_ID_163850182 A-to-I Human chr3 + 173840607 173840607 173840607 AGTCAAGTTGTAAGGGTAGTAAAACCTGGGTTAAGGCTTCAAACAACATATTTTTATCTTTGACT AGTCAAGTTGTAAGGGTAGTAAAACCTGGGTTGAGGCTTCAAACAACATATTTTTATCTTTGACT A G NLGN1 Ensembl:ENSG00000169760 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1002091424 Functional Loss SNV dbSNP153 33..33 33 - - - 25039 RMVar_ID_25039 Human_SNP_ID_163850247 A-to-I Human chr3 + 173840928 173840928 173840928 CCCTAACCCACACGTTAACATCCTCACAACTTAACTTCAGCTTACCTGTACAACCTCATTTCTTC CCCTAACCCACACGTTAACATCCTCACAACTTGACTTCAGCTTACCTGTACAACCTCATTTCTTC A G NLGN1 Ensembl:ENSG00000169760 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1194482879 Functional Loss SNV dbSNP153 33..33 33 - - - 25040 RMVar_ID_25040 Human_SNP_ID_163859122 A-to-I Human chr3 + 173878065 173878065 173878065 GAGAATTATTTTTTTTTTAATCTTTTTGAGACAGAGTCTCGCTCTGTCACCCAGGCTGGAGTGCA GAGAATTATTTTTTTTTTAATCTTTTTGAGACGGAGTCTCGCTCTGTCACCCAGGCTGGAGTGCA A G NLGN1 Ensembl:ENSG00000169760 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs562921432 Functional Loss SNV dbSNP153 33..33 33 - - - 25041 RMVar_ID_25041 Human_SNP_ID_163859123 A-to-I Human chr3 + 173878065 173878065 173878065 GAGAATTATTTTTTTTTTAATCTTTTTGAGACAGAGTCTCGCTCTGTCACCCAGGCTGGAGTGCA GAGAATTATTTTTTTTTTAATCTTTTTGAGACTGAGTCTCGCTCTGTCACCCAGGCTGGAGTGCA A T NLGN1 Ensembl:ENSG00000169760 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs562921432 Functional Loss SNV dbSNP153 33..33 33 - - - 25042 RMVar_ID_25042 Human_SNP_ID_163863216 A-to-I Human chr3 + 173894276 173894276 173894276 CCAACATCAAACACACTACCTAGCAAAAACCTAGGTCGAACCAATGAAGCACCGTGACTTACCAA CCAACATCAAACACACTACCTAGCAAAAACCTGGGTCGAACCAATGAAGCACCGTGACTTACCAA A G NLGN1 Ensembl:ENSG00000169760 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs766654516 Functional Loss SNV dbSNP153 33..33 33 - - - 25043 RMVar_ID_25043 Human_SNP_ID_163863217 A-to-I Human chr3 + 173894276 173894276 173894276 CCAACATCAAACACACTACCTAGCAAAAACCTAGGTCGAACCAATGAAGCACCGTGACTTACCAA CCAACATCAAACACACTACCTAGCAAAAACCTTGGTCGAACCAATGAAGCACCGTGACTTACCAA A T NLGN1 Ensembl:ENSG00000169760 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs766654516 Functional Loss SNV dbSNP153 33..33 33 - - - 25044 RMVar_ID_25044 Human_SNP_ID_163863706 A-to-I Human chr3 + 173896138 173896138 173896138 CTCCATTGGTTCCACTCAGATTTCTGCTAGGTAGTGTGCTTGATTTTGGCCTCTAGTAGGAATAC CTCCATTGGTTCCACTCAGATTTCTGCTAGGTGGTGTGCTTGATTTTGGCCTCTAGTAGGAATAC A G NLGN1 Ensembl:ENSG00000169760 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs926390847 Functional Loss SNV dbSNP153 33..33 33 - - - 25045 RMVar_ID_25045 Human_SNP_ID_163866081 A-to-I Human chr3 + 173906744 173906744 173906744 CATAGTAGGTGCACCCGTAATTCCAGCTACTCAAGAGGCTGACACAGGAGGATCACTTGAGCCTG CATAGTAGGTGCACCCGTAATTCCAGCTACTCCAGAGGCTGACACAGGAGGATCACTTGAGCCTG A C NLGN1 Ensembl:ENSG00000169760 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1203634305 Functional Loss SNV dbSNP153 33..33 33 - - - 25046 RMVar_ID_25046 Human_SNP_ID_163866082 A-to-I Human chr3 + 173906744 173906744 173906744 CATAGTAGGTGCACCCGTAATTCCAGCTACTCAAGAGGCTGACACAGGAGGATCACTTGAGCCTG CATAGTAGGTGCACCCGTAATTCCAGCTACTCGAGAGGCTGACACAGGAGGATCACTTGAGCCTG A G NLGN1 Ensembl:ENSG00000169760 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1203634305 Functional Loss SNV dbSNP153 33..33 33 - - - 25047 RMVar_ID_25047 Human_SNP_ID_163875849 A-to-I Human chr3 + 173947202 173947202 173947202 TTGCCACCACGCCTGGCTAATTTTGCATTTTTAGTAGAGACAGGGTTTCTCCATGTTGATCAGGC TTGCCACCACGCCTGGCTAATTTTGCATTTTTGGTAGAGACAGGGTTTCTCCATGTTGATCAGGC A G NLGN1 Ensembl:ENSG00000169760 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs562602197 Functional Loss SNV dbSNP153 33..33 33 - - - 25048 RMVar_ID_25048 Human_SNP_ID_163876670 A-to-I Human chr3 + 173951006 173951006 173951006 CTCCTGACTCAGCCTCTCGAATAGGTGGGACTACAGGAGTGCGCCACCATGCCTGGCTAATTTTA CTCCTGACTCAGCCTCTCGAATAGGTGGGACTTCAGGAGTGCGCCACCATGCCTGGCTAATTTTA A T NLGN1 Ensembl:ENSG00000169760 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs956433654 Functional Loss SNV dbSNP153 33..33 33 - - - 25049 RMVar_ID_25049 Human_SNP_ID_163898951 A-to-I Human chr3 + 174045030 174045030 174045030 ATTGTGAGTCAATAAATTACCCATTCTTGGGCAGTCCTTTATAGCAGCATGAGAATGGACTAATA ATTGTGAGTCAATAAATTACCCATTCTTGGGCGGTCCTTTATAGCAGCATGAGAATGGACTAATA A G NLGN1 Ensembl:ENSG00000169760 Protein coding intron GSE107867 ASD brains,frontal_cortex;ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1248723535 Functional Loss SNV dbSNP153 33..33 33 - - - 25050 RMVar_ID_25050 Human_SNP_ID_163933463 A-to-I Human chr3 + 174194203 174194203 174194203 TCTCCTGGCCAGGCGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGACGG TCTCCTGGCCAGGCGCGGTGGCTCACACCTGTGATCCCAGCACTTTGGGAGGCTGAGGCAGACGG A G NLGN1 Ensembl:ENSG00000169760 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1233090794 Functional Loss SNV dbSNP153 33..33 33 - - - 25051 RMVar_ID_25051 Human_SNP_ID_163934723 A-to-I Human chr3 + 174199056 174199056 174199056 TTTAGTAGAGACAGTGTTTCCCTATGTTGACCAGGCTGGTCTCGAACTCCCGACTTCAGGTGATC TTTAGTAGAGACAGTGTTTCCCTATGTTGACCGGGCTGGTCTCGAACTCCCGACTTCAGGTGATC A G NLGN1 Ensembl:ENSG00000169760 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1317571427 Functional Loss SNV dbSNP153 33..33 33 - - - 25052 RMVar_ID_25052 Human_SNP_ID_164097011 A-to-I Human chr3 + 174848950 174848950 174848950 CTAGGCTGTAAACCTGTAGAGCATATTACTATACTGAATATTGCAGGCAATTGGAACACGATGGT CTAGGCTGTAAACCTGTAGAGCATATTACTATGCTGAATATTGCAGGCAATTGGAACACGATGGT A G NAALADL2 Ensembl:ENSG00000177694 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1231131191 Functional Loss SNV dbSNP153 33..33 33 - - - 25053 RMVar_ID_25053 Human_SNP_ID_164198166 A-to-I Human chr3 - 175221198 175221198 175221198 AATACTAAAAAATCTTTTTTTTTTTTTTTTTTAAAACGGAGTCTTGCTCTGTCATCCAGGCTAGA AATACTAAAAAATCTTTTTTTTTTTTTTTTTTTAAACGGAGTCTTGCTCTGTCATCCAGGCTAGA T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs936281668 Functional Loss SNV dbSNP153 33..33 33 - - - 25054 RMVar_ID_25054 Human_SNP_ID_164652799 A-to-I Human chr3 - 177026463 177026463 177026463 TTTTGTTTTTCATTCTTTTAGACAGGTGCTCTAGTTCACAGCTATAGGGGAACAGGTGGAATATT TTTTGTTTTTCATTCTTTTAGACAGGTGCTCTGGTTCACAGCTATAGGGGAACAGGTGGAATATT T C TBL1XR1 Ensembl:ENSG00000177565 Protein coding exon GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs544818049 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_595332,Human_RBP_ID_25715694 Human_Splice_Rec_508082,Human_Splice_Rec_508083,Human_Splice_Rec_508112,Human_Splice_Rec_508113,Human_Splice_Rec_508142,Human_Splice_Rec_508143,Human_Splice_Rec_508167,Human_Splice_Rec_508196,Human_Splice_Rec_508197,Human_Splice_Rec_508224,Human_Splice_Rec_508225,Human_Splice_Rec_508252,Human_Splice_Rec_508253,Human_Splice_Rec_508284,Human_Splice_Rec_508285,Human_Splice_Rec_508290,Human_Splice_Rec_508291,Human_Splice_Rec_508293,Human_Splice_Rec_508296 Human_miRNA_ID_1978601 RMVar_hsa_circ_76742,RMVar_hsa_circ_106698,RMVar_hsa_circ_125534,RMVar_hsa_circ_125601,RMVar_hsa_circ_112456,RMVar_hsa_circ_122616,RMVar_hsa_circ_107994,RMVar_hsa_circ_100512,RMVar_hsa_circ_78503,RMVar_hsa_circ_100854,RMVar_hsa_circ_222820,RMVar_hsa_circ_222822,RMVar_hsa_circ_222824,RMVar_hsa_circ_222825,RMVar_hsa_circ_222823,RMVar_hsa_circ_222821,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_17043,RMVar_hsa_circ_38495,RMVar_hsa_circ_222829,RMVar_hsa_circ_222830,RMVar_hsa_circ_222827 25055 RMVar_ID_25055 Human_SNP_ID_164653526 A-to-I Human chr3 - 177029409 177029409 177029409 TGCCATGTTGCCCAGTCTGGCCTCAACCCCCTAGGCTCAAGGGATCCACTTGCCTCAGCCTTCCA TGCCATGTTGCCCAGTCTGGCCTCAACCCCCTGGGCTCAAGGGATCCACTTGCCTCAGCCTTCCA T C TBL1XR1 Ensembl:ENSG00000177565 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1365507260 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76742,RMVar_hsa_circ_106698,RMVar_hsa_circ_125534,RMVar_hsa_circ_125601,RMVar_hsa_circ_112456,RMVar_hsa_circ_122616,RMVar_hsa_circ_107994,RMVar_hsa_circ_100512,RMVar_hsa_circ_222820,RMVar_hsa_circ_222822,RMVar_hsa_circ_222824,RMVar_hsa_circ_222823,RMVar_hsa_circ_222821,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_17043,RMVar_hsa_circ_38495,RMVar_hsa_circ_222829,RMVar_hsa_circ_222827 25056 RMVar_ID_25056 Human_SNP_ID_164653996 A-to-I Human chr3 - 177030949 177030949 177030949 TGCCACCACACCCGGCTAGTTTTGGTATTTTTAGTAGAGATGGAGTTTCACCATGTTGGCCAGGC TGCCACCACACCCGGCTAGTTTTGGTATTTTTGGTAGAGATGGAGTTTCACCATGTTGGCCAGGC T C TBL1XR1 Ensembl:ENSG00000177565 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs946535623 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14730814 RMVar_hsa_circ_76742,RMVar_hsa_circ_106698,RMVar_hsa_circ_125534,RMVar_hsa_circ_125601,RMVar_hsa_circ_112456,RMVar_hsa_circ_122616,RMVar_hsa_circ_107994,RMVar_hsa_circ_100512,RMVar_hsa_circ_222820,RMVar_hsa_circ_222822,RMVar_hsa_circ_222824,RMVar_hsa_circ_222823,RMVar_hsa_circ_222821,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_17043,RMVar_hsa_circ_38495,RMVar_hsa_circ_222829,RMVar_hsa_circ_222827 25057 RMVar_ID_25057 Human_SNP_ID_164654045 A-to-I Human chr3 - 177031125 177031125 177031125 ATACACCCAGCTAAACTTTATTTTTCATTTTTATTTTTATTTTTTGAGATGAAGTCTCGCTCTTG ATACACCCAGCTAAACTTTATTTTTCATTTTTGTTTTTATTTTTTGAGATGAAGTCTCGCTCTTG T C TBL1XR1 Ensembl:ENSG00000177565 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1343379697 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7160717,Human_RBP_ID_14730816 RMVar_hsa_circ_76742,RMVar_hsa_circ_106698,RMVar_hsa_circ_125534,RMVar_hsa_circ_125601,RMVar_hsa_circ_112456,RMVar_hsa_circ_122616,RMVar_hsa_circ_107994,RMVar_hsa_circ_100512,RMVar_hsa_circ_222820,RMVar_hsa_circ_222822,RMVar_hsa_circ_222824,RMVar_hsa_circ_222823,RMVar_hsa_circ_222821,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_17043,RMVar_hsa_circ_38495,RMVar_hsa_circ_222829,RMVar_hsa_circ_222827 25058 RMVar_ID_25058 Human_SNP_ID_164665491 A-to-I Human chr3 - 177072947 177072947 177072947 CGATTCTCCTGCCCCAACCCCCCAAGTAGCTGAGATTACAGGTGCATGCCACCACACCTGGCTAA CGATTCTCCTGCCCCAACCCCCCAAGTAGCTGTGATTACAGGTGCATGCCACCACACCTGGCTAA T A TBL1XR1 Ensembl:ENSG00000177565 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs995697541 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106698,RMVar_hsa_circ_122616,RMVar_hsa_circ_100512,RMVar_hsa_circ_222818,RMVar_hsa_circ_222819,RMVar_hsa_circ_315475,RMVar_hsa_circ_222817,RMVar_hsa_circ_222827,RMVar_hsa_circ_376182,RMVar_hsa_circ_58371,RMVar_hsa_circ_222836,RMVar_hsa_circ_79318,RMVar_hsa_circ_356813,RMVar_hsa_circ_222839,RMVar_hsa_circ_222842,RMVar_hsa_circ_222841,RMVar_hsa_circ_101123,RMVar_hsa_circ_360591,RMVar_hsa_circ_375656,RMVar_hsa_circ_222846,RMVar_hsa_circ_101071,RMVar_hsa_circ_222848,RMVar_hsa_circ_277273,RMVar_hsa_circ_340510,RMVar_hsa_circ_348661,RMVar_hsa_circ_97020,RMVar_hsa_circ_222849,RMVar_hsa_circ_222851,RMVar_hsa_circ_20708,RMVar_hsa_circ_222850 25059 RMVar_ID_25059 Human_SNP_ID_164676781 A-to-I Human chr3 - 177112855 177112855 177112855 GCGACTCCAGGCACATGGTACCACGCCCGACTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCA GCGACTCCAGGCACATGGTACCACGCCCGACTGATTTTTGTATTTTTAGTAGAGACGGGGTTTCA T C TBL1XR1 Ensembl:ENSG00000177565 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1187439573 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106698,RMVar_hsa_circ_100512,RMVar_hsa_circ_222818,RMVar_hsa_circ_222817,RMVar_hsa_circ_101071,RMVar_hsa_circ_222848,RMVar_hsa_circ_97020,RMVar_hsa_circ_222851,RMVar_hsa_circ_20708,RMVar_hsa_circ_314984,RMVar_hsa_circ_222856,RMVar_hsa_circ_222857 25060 RMVar_ID_25060 Human_SNP_ID_164676807 A-to-I Human chr3 - 177112903 177112903 177112903 CGCCTTTCAGATTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGCGACTCCAGGCACATG CGCCTTTCAGATTCAAGCGATTCTCCTGCCTCGGCCTCCCGAGTAGCTGCGACTCCAGGCACATG T C TBL1XR1 Ensembl:ENSG00000177565 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1560189953 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106698,RMVar_hsa_circ_100512,RMVar_hsa_circ_222818,RMVar_hsa_circ_222817,RMVar_hsa_circ_101071,RMVar_hsa_circ_222848,RMVar_hsa_circ_97020,RMVar_hsa_circ_222851,RMVar_hsa_circ_20708,RMVar_hsa_circ_314984,RMVar_hsa_circ_222856,RMVar_hsa_circ_222857 25061 RMVar_ID_25061 Human_SNP_ID_164682384 A-to-I Human chr3 - 177133225 177133225 177133225 TGGAGTGCAGTGGCGCAATCTTAGCTCACTGCAGCCTCTGCCTCCCAGGTTCAAGCTATTCTTGT TGGAGTGCAGTGGCGCAATCTTAGCTCACTGCGGCCTCTGCCTCCCAGGTTCAAGCTATTCTTGT T C TBL1XR1 Ensembl:ENSG00000177565 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251728669 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106698,RMVar_hsa_circ_100512,RMVar_hsa_circ_222818,RMVar_hsa_circ_222817,RMVar_hsa_circ_101071,RMVar_hsa_circ_222848,RMVar_hsa_circ_97020,RMVar_hsa_circ_222851,RMVar_hsa_circ_222857 25062 RMVar_ID_25062 Human_SNP_ID_164689948 A-to-I Human chr3 - 177158411 177158411 177158411 CAGCCTGGCCAACATGGTGAAACTCCGTGTCTACTAAAAATACAAAAATTAGCTGGGCATAGTGG CAGCCTGGCCAACATGGTGAAACTCCGTGTCTGCTAAAAATACAAAAATTAGCTGGGCATAGTGG T C TBL1XR1 Ensembl:ENSG00000177565 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs368992715 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106698,RMVar_hsa_circ_100512,RMVar_hsa_circ_222818,RMVar_hsa_circ_222817,RMVar_hsa_circ_101071,RMVar_hsa_circ_222848,RMVar_hsa_circ_97020,RMVar_hsa_circ_222851 25063 RMVar_ID_25063 Human_SNP_ID_164690450 A-to-I Human chr3 - 177160216 177160216 177160216 CTACCATGACGTCCTCCCAAAGTGCTGGGATTACAGGACTGAGCCACTGCGCCCTACCAGATACT CTACCATGACGTCCTCCCAAAGTGCTGGGATTTCAGGACTGAGCCACTGCGCCCTACCAGATACT T A TBL1XR1 Ensembl:ENSG00000177565 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1321844983 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14733033 RMVar_hsa_circ_106698,RMVar_hsa_circ_100512,RMVar_hsa_circ_222818,RMVar_hsa_circ_222817,RMVar_hsa_circ_101071,RMVar_hsa_circ_222848,RMVar_hsa_circ_97020,RMVar_hsa_circ_222851 25064 RMVar_ID_25064 Human_SNP_ID_164690468 A-to-I Human chr3 - 177160278 177160278 177160278 AGTAGAGATGGGGTTTCATCGTGGTAGCCAGGATGGCCTAGATCTCCTGACGTCATGATGCACTA AGTAGAGATGGGGTTTCATCGTGGTAGCCAGGGTGGCCTAGATCTCCTGACGTCATGATGCACTA T C TBL1XR1 Ensembl:ENSG00000177565 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs977139208 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14733040 RMVar_hsa_circ_106698,RMVar_hsa_circ_100512,RMVar_hsa_circ_222818,RMVar_hsa_circ_222817,RMVar_hsa_circ_101071,RMVar_hsa_circ_222848,RMVar_hsa_circ_97020,RMVar_hsa_circ_222851 25065 RMVar_ID_25065 Human_SNP_ID_164692086 A-to-I Human chr3 - 177166004 177166004 177166004 CTTCCTGCAACCTCCGCCTCCCAGGCTCAAGCAATCCTCCCACCTCAGCCTCCTGAGTAGGTGGG CTTCCTGCAACCTCCGCCTCCCAGGCTCAAGCTATCCTCCCACCTCAGCCTCCTGAGTAGGTGGG T A TBL1XR1 Ensembl:ENSG00000177565 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1022190743 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106698,RMVar_hsa_circ_100512,RMVar_hsa_circ_222818,RMVar_hsa_circ_222817,RMVar_hsa_circ_101071,RMVar_hsa_circ_222848,RMVar_hsa_circ_97020,RMVar_hsa_circ_222851 25066 RMVar_ID_25066 Human_SNP_ID_164692536 A-to-I Human chr3 - 177167714 177167714 177167714 GTTAGTCAGGCTGGTCTCGAACTCCCAACCTTAGGTGATCCGCCTGCCTTGGCCTCCCAGAGTGC GTTAGTCAGGCTGGTCTCGAACTCCCAACCTTCGGTGATCCGCCTGCCTTGGCCTCCCAGAGTGC T G TBL1XR1 Ensembl:ENSG00000177565 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs558830427 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106698,RMVar_hsa_circ_100512,RMVar_hsa_circ_222818,RMVar_hsa_circ_222817,RMVar_hsa_circ_101071,RMVar_hsa_circ_222848,RMVar_hsa_circ_97020,RMVar_hsa_circ_222851 25067 RMVar_ID_25067 Human_SNP_ID_164692542 A-to-I Human chr3 - 177167743 177167743 177167743 TATTTTTAGTAGAGATGGGGTTTTTCCATGTTAGTCAGGCTGGTCTCGAACTCCCAACCTTAGGT TATTTTTAGTAGAGATGGGGTTTTTCCATGTTGGTCAGGCTGGTCTCGAACTCCCAACCTTAGGT T C TBL1XR1 Ensembl:ENSG00000177565 Protein coding intron GSE38233;GSE107867 cultured B-cells;ASD brains,frontal_cortex - 24183664,30559470 RNA-Seq:(High) rs1381075743 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14992007 RMVar_hsa_circ_106698,RMVar_hsa_circ_100512,RMVar_hsa_circ_222818,RMVar_hsa_circ_222817,RMVar_hsa_circ_101071,RMVar_hsa_circ_222848,RMVar_hsa_circ_97020,RMVar_hsa_circ_222851 25068 RMVar_ID_25068 Human_SNP_ID_164692813 A-to-I Human chr3 - 177168568 177168568 177168568 CCTTTAGAAAACGGTTCATGGCCGGACGTGGTAGCTCACCCCTGTAATCCCAGCACTTTGGGAGG CCTTTAGAAAACGGTTCATGGCCGGACGTGGTGGCTCACCCCTGTAATCCCAGCACTTTGGGAGG T C TBL1XR1 Ensembl:ENSG00000177565 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1173256796 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14733305 RMVar_hsa_circ_106698,RMVar_hsa_circ_100512,RMVar_hsa_circ_222818,RMVar_hsa_circ_222817,RMVar_hsa_circ_101071,RMVar_hsa_circ_222848,RMVar_hsa_circ_97020,RMVar_hsa_circ_222851 25069 RMVar_ID_25069 Human_SNP_ID_164693366 A-to-I Human chr3 - 177170716 177170716 177170716 CCTGTATTCCCAGGTACTTGGTGGGCAGAGGCAGGAAGATTGCTTGAGCTGGGGAAGTGGAGACT CCTGTATTCCCAGGTACTTGGTGGGCAGAGGCGGGAAGATTGCTTGAGCTGGGGAAGTGGAGACT T C TBL1XR1 Ensembl:ENSG00000177565 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs912519384 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14733352 RMVar_hsa_circ_106698,RMVar_hsa_circ_100512,RMVar_hsa_circ_222818,RMVar_hsa_circ_222817,RMVar_hsa_circ_101071,RMVar_hsa_circ_222848,RMVar_hsa_circ_97020,RMVar_hsa_circ_222851 25070 RMVar_ID_25070 Human_SNP_ID_164693372 A-to-I Human chr3 - 177170743 177170743 177170743 AAAACTAGCTGGGCATGGTGGTGCATGCCTGTATTCCCAGGTACTTGGTGGGCAGAGGCAGGAAG AAAACTAGCTGGGCATGGTGGTGCATGCCTGTTTTCCCAGGTACTTGGTGGGCAGAGGCAGGAAG T A TBL1XR1 Ensembl:ENSG00000177565 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs909722814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25716317 RMVar_hsa_circ_106698,RMVar_hsa_circ_100512,RMVar_hsa_circ_222818,RMVar_hsa_circ_222817,RMVar_hsa_circ_101071,RMVar_hsa_circ_222848,RMVar_hsa_circ_97020,RMVar_hsa_circ_222851 25071 RMVar_ID_25071 Human_SNP_ID_164693379 A-to-I Human chr3 - 177170761 177170761 177170761 GTCTCAACAAAAAATACAAAAACTAGCTGGGCATGGTGGTGCATGCCTGTATTCCCAGGTACTTG GTCTCAACAAAAAATACAAAAACTAGCTGGGCGTGGTGGTGCATGCCTGTATTCCCAGGTACTTG T C TBL1XR1 Ensembl:ENSG00000177565 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991429569 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106698,RMVar_hsa_circ_100512,RMVar_hsa_circ_222818,RMVar_hsa_circ_222817,RMVar_hsa_circ_101071,RMVar_hsa_circ_222848,RMVar_hsa_circ_97020,RMVar_hsa_circ_222851 25072 RMVar_ID_25072 Human_SNP_ID_164693407 A-to-I Human chr3 - 177170877 177170877 177170877 CATGATCATTGGCACGGTGGCTCATGCCTGCAATCCCAGCACTTTGGGAGGCTGAGGTGGGTGGA CATGATCATTGGCACGGTGGCTCATGCCTGCAGTCCCAGCACTTTGGGAGGCTGAGGTGGGTGGA T C TBL1XR1 Ensembl:ENSG00000177565 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1056389593 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106698,RMVar_hsa_circ_100512,RMVar_hsa_circ_222818,RMVar_hsa_circ_222817,RMVar_hsa_circ_101071,RMVar_hsa_circ_222848,RMVar_hsa_circ_97020,RMVar_hsa_circ_222851 25073 RMVar_ID_25073 Human_SNP_ID_164696343 A-to-I Human chr3 - 177180155 177180155 177180155 TCAGCTCACTGCAACCCACGCCTCCCGGATTCAGGCAATTCTCCTGCCCCAGCCTCCCAAGTAGC TCAGCTCACTGCAACCCACGCCTCCCGGATTCGGGCAATTCTCCTGCCCCAGCCTCCCAAGTAGC T C TBL1XR1 Ensembl:ENSG00000177565 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1018789571 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14733655 RMVar_hsa_circ_106698,RMVar_hsa_circ_100512,RMVar_hsa_circ_222818,RMVar_hsa_circ_222817,RMVar_hsa_circ_101071,RMVar_hsa_circ_222848,RMVar_hsa_circ_97020,RMVar_hsa_circ_222851 25074 RMVar_ID_25074 Human_SNP_ID_164696605 A-to-I Human chr3 - 177180874 177180864 177180875 TACAAAAAACTAGCAGGGCGTGGTGGCCTGTAATCGTAGCTACTCCAGAGGCTGAGGCAGGAGAA TACAAAAAACTAGCAGGGCGTGGTGGCCTGT___________CTCCAGAGGCTGAGGCAGGAGAA GTAGCTACGATT G TBL1XR1 Ensembl:ENSG00000177565 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1173367552 Functional Loss DEL dbSNP153 32..42 33 - - - Human_RBP_ID_23986217 RMVar_hsa_circ_106698,RMVar_hsa_circ_100512,RMVar_hsa_circ_222818,RMVar_hsa_circ_222817,RMVar_hsa_circ_101071,RMVar_hsa_circ_222848,RMVar_hsa_circ_97020,RMVar_hsa_circ_222851 25075 RMVar_ID_25075 Human_SNP_ID_164696605 A-to-I Human chr3 - 177180875 177180864 177180875 ATACAAAAAACTAGCAGGGCGTGGTGGCCTGTAATCGTAGCTACTCCAGAGGCTGAGGCAGGAGA ATACAAAAAACTAGCAGGGCGTGGTGGCCTGT___________CTCCAGAGGCTGAGGCAGGAGA GTAGCTACGATT G TBL1XR1 Ensembl:ENSG00000177565 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1173367552 Functional Loss DEL dbSNP153 33..43 33 - - - Human_RBP_ID_23986217 RMVar_hsa_circ_106698,RMVar_hsa_circ_100512,RMVar_hsa_circ_222818,RMVar_hsa_circ_222817,RMVar_hsa_circ_101071,RMVar_hsa_circ_222848,RMVar_hsa_circ_97020,RMVar_hsa_circ_222851 25076 RMVar_ID_25076 Human_SNP_ID_164696606 A-to-I Human chr3 - 177180874 177180868 177180874 TACAAAAAACTAGCAGGGCGTGGTGGCCTGTAATCGTAGCTACTCCAGAGGCTGAGGCAGGAGAA TACAAAAAACTAGCAGGGCGTGGTGGCCTGTA______GCTACTCCAGAGGCTGAGGCAGGAGAA CTACGAT C TBL1XR1 Ensembl:ENSG00000177565 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1456025351 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_23986217 RMVar_hsa_circ_106698,RMVar_hsa_circ_100512,RMVar_hsa_circ_222818,RMVar_hsa_circ_222817,RMVar_hsa_circ_101071,RMVar_hsa_circ_222848,RMVar_hsa_circ_97020,RMVar_hsa_circ_222851 25077 RMVar_ID_25077 Human_SNP_ID_164696626 A-to-I Human chr3 - 177180951 177180951 177180951 AGGTGGGTGGATCACCTGAGGTCAGGAGTTCAAGACCAGCCTGACCAACATGGTGAAACCCCCGT AGGTGGGTGGATCACCTGAGGTCAGGAGTTCAGGACCAGCCTGACCAACATGGTGAAACCCCCGT T C TBL1XR1 Ensembl:ENSG00000177565 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs576582553 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106698,RMVar_hsa_circ_100512,RMVar_hsa_circ_222818,RMVar_hsa_circ_222817,RMVar_hsa_circ_101071,RMVar_hsa_circ_222848,RMVar_hsa_circ_97020,RMVar_hsa_circ_222851 25078 RMVar_ID_25078 Human_SNP_ID_164696729 A-to-I Human chr3 - 177181314 177181314 177181314 CACCACACCTGGCTAATTTTTGTATTACTAGTAGAGATGGGGTTTCACCGTGTTGGCCAGGCTGG CACCACACCTGGCTAATTTTTGTATTACTAGTGGAGATGGGGTTTCACCGTGTTGGCCAGGCTGG T C TBL1XR1 Ensembl:ENSG00000177565 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1391795764 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106698,RMVar_hsa_circ_100512,RMVar_hsa_circ_222818,RMVar_hsa_circ_222817,RMVar_hsa_circ_101071,RMVar_hsa_circ_222848,RMVar_hsa_circ_97020,RMVar_hsa_circ_222851 25079 RMVar_ID_25079 Human_SNP_ID_164696785 A-to-I Human chr3 - 177181479 177181479 177181479 GGCTGGCAGAGGCGTTCTTTTTTTTTTTTTTTAAGACGGAGTCTGGCTCTGTCACTCAGGCTGGA GGCTGGCAGAGGCGTTCTTTTTTTTTTTTTTTTAGACGGAGTCTGGCTCTGTCACTCAGGCTGGA T A TBL1XR1 Ensembl:ENSG00000177565 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1394884060 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14733688,Human_RBP_ID_23986218 RMVar_hsa_circ_106698,RMVar_hsa_circ_100512,RMVar_hsa_circ_222818,RMVar_hsa_circ_222817,RMVar_hsa_circ_101071,RMVar_hsa_circ_222848,RMVar_hsa_circ_97020,RMVar_hsa_circ_222851 25080 RMVar_ID_25080 Human_SNP_ID_164697039 A-to-I Human chr3 - 177182292 177182292 177182292 CAGCCCTGAACTCCCCGGGCTCAGGTGGTCCTATCACCTCAGCCTCTTGAGTATCTGGGACTACT CAGCCCTGAACTCCCCGGGCTCAGGTGGTCCTGTCACCTCAGCCTCTTGAGTATCTGGGACTACT T C TBL1XR1 Ensembl:ENSG00000177565 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1997394 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2713010,Human_miRNA_ID_3048988 GWAS_ID_2353,GWAS_ID_2354,GWAS_ID_2355,GWAS_ID_2356,GWAS_ID_2357,GWAS_ID_2358,GWAS_ID_2359,GWAS_ID_2360,GWAS_ID_2361,GWAS_ID_2362,GWAS_ID_2363,GWAS_ID_2364,GWAS_ID_2365,GWAS_ID_2366,GWAS_ID_2367,GWAS_ID_2368,GWAS_ID_2369,GWAS_ID_2370,GWAS_ID_2371,GWAS_ID_2372,GWAS_ID_2373,GWAS_ID_2374,GWAS_ID_2375,GWAS_ID_2376,GWAS_ID_2377,GWAS_ID_2378,GWAS_ID_2379,GWAS_ID_2380,GWAS_ID_2381,GWAS_ID_2382,GWAS_ID_2383,GWAS_ID_2384,GWAS_ID_2385,GWAS_ID_2386,GWAS_ID_2387,GWAS_ID_2388,GWAS_ID_2389,GWAS_ID_2390,GWAS_ID_2391 RMVar_hsa_circ_106698,RMVar_hsa_circ_100512,RMVar_hsa_circ_222818,RMVar_hsa_circ_222817,RMVar_hsa_circ_101071,RMVar_hsa_circ_222848,RMVar_hsa_circ_97020,RMVar_hsa_circ_222851 25081 RMVar_ID_25081 Human_SNP_ID_164698831 A-to-I Human chr3 - 177188025 177188025 177188025 TGTTAGCCTGAACCTGGGAGGTGGAGGTTGCCATGAGCTGAGATCGTGCCACTGTATTCCTGCCT TGTTAGCCTGAACCTGGGAGGTGGAGGTTGCCGTGAGCTGAGATCGTGCCACTGTATTCCTGCCT T C TBL1XR1 Ensembl:ENSG00000177565 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1347452378 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10082618,Human_RBP_ID_14733988,Human_RBP_ID_25716414 RMVar_hsa_circ_106698,RMVar_hsa_circ_100512,RMVar_hsa_circ_222818,RMVar_hsa_circ_222817,RMVar_hsa_circ_101071,RMVar_hsa_circ_222848,RMVar_hsa_circ_97020,RMVar_hsa_circ_222851 25082 RMVar_ID_25082 Human_SNP_ID_164698980 A-to-I Human chr3 - 177188508 177188508 177188508 AGGTTTGCTCTTGTTGCCCAGGCTGGAGTGCAATGGCGCAATTTTGGCTCACTGCACCCTCCACC AGGTTTGCTCTTGTTGCCCAGGCTGGAGTGCAGTGGCGCAATTTTGGCTCACTGCACCCTCCACC T C TBL1XR1 Ensembl:ENSG00000177565 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs527420479 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14733996,Human_RBP_ID_17574164 RMVar_hsa_circ_106698,RMVar_hsa_circ_100512,RMVar_hsa_circ_222818,RMVar_hsa_circ_222817,RMVar_hsa_circ_101071,RMVar_hsa_circ_222848,RMVar_hsa_circ_97020,RMVar_hsa_circ_222851 25083 RMVar_ID_25083 Human_SNP_ID_164700020 A-to-I Human chr3 - 177191620 177191620 177191620 GTCCTTAGAAGTTCAGTTCCTCTATGAGCCTTATCTTATGTTCACTTCCCATTTTTAACCATACT GTCCTTAGAAGTTCAGTTCCTCTATGAGCCTTGTCTTATGTTCACTTCCCATTTTTAACCATACT T C TBL1XR1 Ensembl:ENSG00000177565 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6790639 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10082644,Human_RBP_ID_25716450 GWAS_ID_2392,GWAS_ID_2393,GWAS_ID_2394,GWAS_ID_2395,GWAS_ID_2396,GWAS_ID_2397,GWAS_ID_2398,GWAS_ID_2399,GWAS_ID_2400,GWAS_ID_2401,GWAS_ID_2402,GWAS_ID_2403,GWAS_ID_2404,GWAS_ID_2405,GWAS_ID_2406,GWAS_ID_2407,GWAS_ID_2408,GWAS_ID_2409,GWAS_ID_2410,GWAS_ID_2411,GWAS_ID_2412,GWAS_ID_2413,GWAS_ID_2414,GWAS_ID_2415,GWAS_ID_2416,GWAS_ID_2417,GWAS_ID_2418,GWAS_ID_2419,GWAS_ID_2420,GWAS_ID_2421,GWAS_ID_2422,GWAS_ID_2423,GWAS_ID_2424 RMVar_hsa_circ_106698,RMVar_hsa_circ_100512,RMVar_hsa_circ_222818,RMVar_hsa_circ_222817,RMVar_hsa_circ_101071,RMVar_hsa_circ_222848,RMVar_hsa_circ_97020,RMVar_hsa_circ_222851 25084 RMVar_ID_25084 Human_SNP_ID_164700114 A-to-I Human chr3 - 177191913 177191913 177191913 ATTTCTTGTATCTTTAGTAGAGATGGGGTTTCACCATGTTGGTCAGGCTGGTCTCGAACTCCTGA ATTTCTTGTATCTTTAGTAGAGATGGGGTTTCGCCATGTTGGTCAGGCTGGTCTCGAACTCCTGA T C TBL1XR1 Ensembl:ENSG00000177565 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs897389197 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106698,RMVar_hsa_circ_100512,RMVar_hsa_circ_222818,RMVar_hsa_circ_222817,RMVar_hsa_circ_101071,RMVar_hsa_circ_222848,RMVar_hsa_circ_97020,RMVar_hsa_circ_222851 25085 RMVar_ID_25085 Human_SNP_ID_164700145 A-to-I Human chr3 - 177191998 177191998 177191998 ACCTCTGCCTCCCGGGTTCAAGCGATTCCCCTACCTCAGCCTCCCAAGTAGCTGGGATTACAGGC ACCTCTGCCTCCCGGGTTCAAGCGATTCCCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGC T C TBL1XR1 Ensembl:ENSG00000177565 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1559971987 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25716458 Human_miRNA_ID_1913593,Human_miRNA_ID_1916043,Human_miRNA_ID_1918491,Human_miRNA_ID_1920948,Human_miRNA_ID_1923405,Human_miRNA_ID_1925856,Human_miRNA_ID_1928306,Human_miRNA_ID_1930759,Human_miRNA_ID_2628588,Human_miRNA_ID_2641698,Human_miRNA_ID_2713013,Human_miRNA_ID_3048991,Human_miRNA_ID_3124440 RMVar_hsa_circ_106698,RMVar_hsa_circ_100512,RMVar_hsa_circ_222818,RMVar_hsa_circ_222817,RMVar_hsa_circ_101071,RMVar_hsa_circ_222848,RMVar_hsa_circ_97020,RMVar_hsa_circ_222851 25086 RMVar_ID_25086 Human_SNP_ID_164700148 A-to-I Human chr3 - 177192006 177192006 177192006 TCACTGCAACCTCTGCCTCCCGGGTTCAAGCGATTCCCCTACCTCAGCCTCCCAAGTAGCTGGGA TCACTGCAACCTCTGCCTCCCGGGTTCAAGCGGTTCCCCTACCTCAGCCTCCCAAGTAGCTGGGA T C TBL1XR1 Ensembl:ENSG00000177565 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1370266663 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1913593,Human_miRNA_ID_1916043,Human_miRNA_ID_1918491,Human_miRNA_ID_1920948,Human_miRNA_ID_1923405,Human_miRNA_ID_1925856,Human_miRNA_ID_1928306,Human_miRNA_ID_1930759,Human_miRNA_ID_2628588,Human_miRNA_ID_2641698,Human_miRNA_ID_2713013,Human_miRNA_ID_3048991,Human_miRNA_ID_3124440 RMVar_hsa_circ_106698,RMVar_hsa_circ_100512,RMVar_hsa_circ_222818,RMVar_hsa_circ_222817,RMVar_hsa_circ_101071,RMVar_hsa_circ_222848,RMVar_hsa_circ_97020,RMVar_hsa_circ_222851 25087 RMVar_ID_25087 Human_SNP_ID_164700766 A-to-I Human chr3 - 177193735 177193735 177193735 GTAGATCATCCTTCCAAAAACTTGTGTTTCTAATCAAGTTTATGATCTATAGTTGAGCGTCTGTA GTAGATCATCCTTCCAAAAACTTGTGTTTCTAGTCAAGTTTATGATCTATAGTTGAGCGTCTGTA T C TBL1XR1 Ensembl:ENSG00000177565 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs35072945 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22702190,Human_RBP_ID_23986279 RMVar_hsa_circ_106698,RMVar_hsa_circ_100512,RMVar_hsa_circ_222818,RMVar_hsa_circ_222817,RMVar_hsa_circ_101071,RMVar_hsa_circ_222848,RMVar_hsa_circ_97020,RMVar_hsa_circ_222851 25088 RMVar_ID_25088 Human_SNP_ID_165101142 A-to-I Human chr3 - 178840192 178840192 178840192 CCCGAATGTGAGACATGGAGTCAAAGGAGATTATTTTGGAACTTTAAGATTTAATGACTGCCTGT CCCGAATGTGAGACATGGAGTCAAAGGAGATTGTTTTGGAACTTTAAGATTTAATGACTGCCTGT T C KCNMB2-AS1 Ensembl:ENSG00000237978 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1240104723 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125376,RMVar_hsa_circ_222862 25089 RMVar_ID_25089 Human_SNP_ID_165127665 A-to-I Human chr3 - 178949964 178949964 178949964 TACATCATACTTGATAAATAAATGACTGTATTAGTCCGTTCTCATGCTGCTAATAAAGACGTACC TACATCATACTTGATAAATAAATGACTGTATTTGTCCGTTCTCATGCTGCTAATAAAGACGTACC T A lnc-ZMAT3-5,KCNMB2-AS1 RNACentral:URS00009B168A,RNACentral:URS00009C5640 lincRNA,lincRNA exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs944744422 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1956359,Human_RBP_ID_3697739 25090 RMVar_ID_25090 Human_SNP_ID_165139062 A-to-I Human chr3 - 179001108 179001108 179001108 TTGTAAAAAGGCAGAGGGTCCACTGGTTAACAATTAAGCTGTCTGTGGATGGCAAGGCTAAAAGA TTGTAAAAAGGCAGAGGGTCCACTGGTTAACAGTTAAGCTGTCTGTGGATGGCAAGGCTAAAAGA T C ZMAT3 Ensembl:ENSG00000172667 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs535673425 Functional Loss SNV dbSNP153 33..33 33 - - - 25091 RMVar_ID_25091 Human_SNP_ID_165139077 A-to-I Human chr3 - 179001170 179001170 179001170 CTTCTTCTGGGATGCTGGACTCTTGTCGGGATACAGAAAGCTGTCACACTGGCCCTCTGCCGTTG CTTCTTCTGGGATGCTGGACTCTTGTCGGGATGCAGAAAGCTGTCACACTGGCCCTCTGCCGTTG T C ZMAT3 Ensembl:ENSG00000172667 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs773760886 Functional Loss SNV dbSNP153 33..33 33 - - - 25092 RMVar_ID_25092 Human_SNP_ID_165145535 A-to-I Human chr3 - 179029120 179029120 179029120 AGTTTTGCTCTTGTTGCCCAGGCTGGAGTGCAATGGTGTGCTGGGCTCACTGCAACCTCCGCCTC AGTTTTGCTCTTGTTGCCCAGGCTGGAGTGCAGTGGTGTGCTGGGCTCACTGCAACCTCCGCCTC T C ZMAT3 Ensembl:ENSG00000172667 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs371966171 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82016,RMVar_hsa_circ_103963,RMVar_hsa_circ_222868,RMVar_hsa_circ_107005,RMVar_hsa_circ_222869,RMVar_hsa_circ_222870 25093 RMVar_ID_25093 Human_SNP_ID_165177846 A-to-I Human chr3 + 179160745 179160745 179160745 ATTATATCTTTGTACAACACACAATTTTGTACAGTGTGGTATACAAAAACCACATACATTATACT ATTATATCTTTGTACAACACACAATTTTGTACGGTGTGGTATACAAAAACCACATACATTATACT A G PIK3CA Ensembl:ENSG00000121879 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs143890209 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17573463 25094 RMVar_ID_25094 Human_SNP_ID_165177850 A-to-I Human chr3 + 179160766 179160766 179160766 CAATTTTGTACAGTGTGGTATACAAAAACCACATACATTATACTTTATGGATGACTTGAGATTTT CAATTTTGTACAGTGTGGTATACAAAAACCACGTACATTATACTTTATGGATGACTTGAGATTTT A G PIK3CA Ensembl:ENSG00000121879 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559214528 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17573463 25095 RMVar_ID_25095 Human_SNP_ID_165184205 A-to-I Human chr3 + 179187917 179187917 179187917 CCTCGGCCTCCCAAAATGCTGGGATTATAGGCATGAGCCACCATGCCCGACCCTCATTTAATTCT CCTCGGCCTCCCAAAATGCTGGGATTATAGGCGTGAGCCACCATGCCCGACCCTCATTTAATTCT A G PIK3CA Ensembl:ENSG00000121879 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs767760912 Functional Loss SNV dbSNP153 33..33 33 - - - 25096 RMVar_ID_25096 Human_SNP_ID_165197938 A-to-I Human chr3 - 179249629 179249629 179249629 CTTGCTCTGTCGCCAGGCTGGAGTGCAGTGGCACGATCTTGGCTCACTGCAACCTCTGCCTCCCG CTTGCTCTGTCGCCAGGCTGGAGTGCAGTGGCTCGATCTTGGCTCACTGCAACCTCTGCCTCCCG T A KCNMB3 Ensembl:ENSG00000171121 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1015301278 Functional Loss SNV dbSNP153 33..33 33 - - - 25097 RMVar_ID_25097 Human_SNP_ID_165198549 A-to-I Human chr3 - 179251915 179251915 179251915 GCGTTCGAGACCATTATGGCCAACATGGTGAAACACTGTCTCTACTTAAAATACAAAAATTAGCT GCGTTCGAGACCATTATGGCCAACATGGTGAAGCACTGTCTCTACTTAAAATACAAAAATTAGCT T C KCNMB3 Ensembl:ENSG00000171121 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs769895754 Functional Loss SNV dbSNP153 33..33 33 - - - 25098 RMVar_ID_25098 Human_SNP_ID_165199291 A-to-I Human chr3 - 179255070 179255070 179255070 ACATCCACCTTCTGGGTTCAAGTGATTGTCCCACCTCAGCCTCCCGAGTAGCTGGGATTACAGGT ACATCCACCTTCTGGGTTCAAGTGATTGTCCCCCCTCAGCCTCCCGAGTAGCTGGGATTACAGGT T G KCNMB3 Ensembl:ENSG00000171121 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1039136396 Functional Loss SNV dbSNP153 33..33 33 - - - 25099 RMVar_ID_25099 Human_SNP_ID_165199311 A-to-I Human chr3 - 179255163 179255162 179255163 TTATTATGTATTTATTTATTCATTTTTTTTTGAGATAGAGTCTTGCTCTGTTGCCCAGACTGAAG TTATTATGTATTTATTTATTCATTTTTTTTTG_GATAGAGTCTTGCTCTGTTGCCCAGACTGAAG CT C KCNMB3 Ensembl:ENSG00000171121 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1412128789 Functional Loss DEL dbSNP153 33..33 33 - - - 25100 RMVar_ID_25100 Human_SNP_ID_165199312 A-to-I Human chr3 - 179255163 179255163 179255163 TTATTATGTATTTATTTATTCATTTTTTTTTGAGATAGAGTCTTGCTCTGTTGCCCAGACTGAAG TTATTATGTATTTATTTATTCATTTTTTTTTGTGATAGAGTCTTGCTCTGTTGCCCAGACTGAAG T A KCNMB3 Ensembl:ENSG00000171121 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1286824501 Functional Loss SNV dbSNP153 33..33 33 - - - 25101 RMVar_ID_25101 Human_SNP_ID_165217021 A-to-I Human chr3 + 179325052 179325052 179325052 TCTTTCTTTCTTTCTTTTTTAGACAGAGTTTCACTCCTGTTACCCAGGCTGGAGGACAATGATGT TCTTTCTTTCTTTCTTTTTTAGACAGAGTTTCCCTCCTGTTACCCAGGCTGGAGGACAATGATGT A C ZNF639 Ensembl:ENSG00000121864 Protein coding intron GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs1289418829 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25763383 Human_Splice_Rec_508970,Human_Splice_Rec_508994 25102 RMVar_ID_25102 Human_SNP_ID_165217059 A-to-I Human chr3 + 179325187 179325187 179325187 CAGATTACAGGCATGTGCCACCACGCCCGGCTAATTTTGTATTTTCAGTCGAGACGGGGTTTCCC CAGATTACAGGCATGTGCCACCACGCCCGGCTGATTTTGTATTTTCAGTCGAGACGGGGTTTCCC A G ZNF639 Ensembl:ENSG00000121864 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1216501620 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_784413,Human_RBP_ID_14735790 25103 RMVar_ID_25103 Human_SNP_ID_165217063 A-to-I Human chr3 + 179325201 179325201 179325201 GTGCCACCACGCCCGGCTAATTTTGTATTTTCAGTCGAGACGGGGTTTCCCCATGTTGGTCAGGC GTGCCACCACGCCCGGCTAATTTTGTATTTTCCGTCGAGACGGGGTTTCCCCATGTTGGTCAGGC A C ZNF639 Ensembl:ENSG00000121864 Protein coding intron GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs967697688 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_784413,Human_RBP_ID_4731685,Human_RBP_ID_14735791,Human_RBP_ID_27049297 25104 RMVar_ID_25104 Human_SNP_ID_165217064 A-to-I Human chr3 + 179325201 179325201 179325201 GTGCCACCACGCCCGGCTAATTTTGTATTTTCAGTCGAGACGGGGTTTCCCCATGTTGGTCAGGC GTGCCACCACGCCCGGCTAATTTTGTATTTTCGGTCGAGACGGGGTTTCCCCATGTTGGTCAGGC A G ZNF639 Ensembl:ENSG00000121864 Protein coding intron GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs967697688 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_784413,Human_RBP_ID_4731685,Human_RBP_ID_14735791,Human_RBP_ID_27049297 25105 RMVar_ID_25105 Human_SNP_ID_165217317 A-to-I Human chr3 + 179326149 179326149 179326149 GGTCAGGAGTTCAAGACCAGCCTGGCTAACATAGTAAACCCCCGTCTCTACTAAAAATACAAAAA GGTCAGGAGTTCAAGACCAGCCTGGCTAACATGGTAAACCCCCGTCTCTACTAAAAATACAAAAA A G ZNF639 Ensembl:ENSG00000121864 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1423481757 Functional Loss SNV dbSNP153 33..33 33 - - - 25106 RMVar_ID_25106 Human_SNP_ID_165217459 A-to-I Human chr3 + 179326719 179326719 179326719 CGATGTCAGCTCACTGTAGCCCTCCGCCTCCCAGGTTCAAGCCATTCTCCTGCCTCAGCCTCTTG CGATGTCAGCTCACTGTAGCCCTCCGCCTCCCGGGTTCAAGCCATTCTCCTGCCTCAGCCTCTTG A G ZNF639 Ensembl:ENSG00000121864 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559549908 Functional Loss SNV dbSNP153 33..33 33 - - - 25107 RMVar_ID_25107 Human_SNP_ID_165217460 A-to-I Human chr3 + 179326719 179326719 179326722 CGATGTCAGCTCACTGTAGCCCTCCGCCTCCCAGGTTCAAGCCATTCTCCTGCCTCAGCCTCTTG CGATGTCAGCTCACTGTAGCCCTCCGCCTCCCCAGCTCAAGCCATTCTCCTGCCTCAGCCTCTTG AGGT CAGC ZNF639 Ensembl:ENSG00000121864 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs796992556 Functional Loss MNV dbSNP153 33..36 33 - - - 25108 RMVar_ID_25108 Human_SNP_ID_165223548 A-to-I Human chr3 + 179349675 179349675 179349675 GGACTACAGTGCACGTGCCACCATGCCTGACTAATTTTTGTGTTTTTAGTAGAGACAGGGTTTCA GGACTACAGTGCACGTGCCACCATGCCTGACTGATTTTTGTGTTTTTAGTAGAGACAGGGTTTCA A G MFN1 Ensembl:ENSG00000171109 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs574986607 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_65617,RMVar_hsa_circ_116507,RMVar_hsa_circ_320275,RMVar_hsa_circ_340248,RMVar_hsa_circ_106314,RMVar_hsa_circ_222899,RMVar_hsa_circ_222900 25109 RMVar_ID_25109 Human_SNP_ID_165229206 A-to-I Human chr3 + 179371390 179371390 179371390 AAAAAAAAATCCAGATATGATAGCTCATGACTATAGTCACAGCTACCCCAGAGGCTGAGGTAGAA AAAAAAAAATCCAGATATGATAGCTCATGACTGTAGTCACAGCTACCCCAGAGGCTGAGGTAGAA A G MFN1 Ensembl:ENSG00000171109 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1169904260 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9136415 RMVar_hsa_circ_5521,RMVar_hsa_circ_65617,RMVar_hsa_circ_116507,RMVar_hsa_circ_340248,RMVar_hsa_circ_222900,RMVar_hsa_circ_357426,RMVar_hsa_circ_298787,RMVar_hsa_circ_21158,RMVar_hsa_circ_222903,RMVar_hsa_circ_222901,RMVar_hsa_circ_222902,RMVar_hsa_circ_308903,RMVar_hsa_circ_305877,RMVar_hsa_circ_222904,RMVar_hsa_circ_332119,RMVar_hsa_circ_335915 25110 RMVar_ID_25110 Human_SNP_ID_165229219 A-to-I Human chr3 + 179371458 179371458 179371458 CAAGAAGTTTGAGGCTGTGGTGATGGTGAGCTATGGAGGTACCACTGTGCTCCAACCTGTGTGAC CAAGAAGTTTGAGGCTGTGGTGATGGTGAGCTGTGGAGGTACCACTGTGCTCCAACCTGTGTGAC A G MFN1 Ensembl:ENSG00000171109 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs539661931 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9136416,Human_RBP_ID_14736253 RMVar_hsa_circ_5521,RMVar_hsa_circ_65617,RMVar_hsa_circ_116507,RMVar_hsa_circ_340248,RMVar_hsa_circ_222900,RMVar_hsa_circ_357426,RMVar_hsa_circ_298787,RMVar_hsa_circ_21158,RMVar_hsa_circ_222903,RMVar_hsa_circ_222901,RMVar_hsa_circ_222902,RMVar_hsa_circ_308903,RMVar_hsa_circ_305877,RMVar_hsa_circ_222904,RMVar_hsa_circ_332119,RMVar_hsa_circ_335915,RMVar_hsa_circ_222905 25111 RMVar_ID_25111 Human_SNP_ID_165229731 A-to-I Human chr3 + 179373743 179373743 179373743 TCGCCCAGGCTGGAGTGCAGTGGCGCTATCTCAGCTCACTGCAAGCTCCACCTTCCGGGTTCTCG TCGCCCAGGCTGGAGTGCAGTGGCGCTATCTCGGCTCACTGCAAGCTCCACCTTCCGGGTTCTCG A G MFN1 Ensembl:ENSG00000171109 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs192954179 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5521,RMVar_hsa_circ_65617,RMVar_hsa_circ_116507,RMVar_hsa_circ_340248,RMVar_hsa_circ_222900,RMVar_hsa_circ_357426,RMVar_hsa_circ_298787,RMVar_hsa_circ_21158,RMVar_hsa_circ_222903,RMVar_hsa_circ_222901,RMVar_hsa_circ_222902,RMVar_hsa_circ_308903,RMVar_hsa_circ_305877,RMVar_hsa_circ_332119,RMVar_hsa_circ_335915 25112 RMVar_ID_25112 Human_SNP_ID_165229833 A-to-I Human chr3 + 179374141 179374141 179374141 CCTGGCCAACACTGCAAAACCCTAACTCTACTAAAAATGTAAAAATTAGCCAGGCATAGTGGTGC CCTGGCCAACACTGCAAAACCCTAACTCTACTGAAAATGTAAAAATTAGCCAGGCATAGTGGTGC A G MFN1 Ensembl:ENSG00000171109 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1401096481 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5521,RMVar_hsa_circ_65617,RMVar_hsa_circ_116507,RMVar_hsa_circ_340248,RMVar_hsa_circ_222900,RMVar_hsa_circ_357426,RMVar_hsa_circ_298787,RMVar_hsa_circ_21158,RMVar_hsa_circ_222903,RMVar_hsa_circ_222901,RMVar_hsa_circ_222902,RMVar_hsa_circ_308903,RMVar_hsa_circ_305877,RMVar_hsa_circ_332119,RMVar_hsa_circ_335915 25113 RMVar_ID_25113 Human_SNP_ID_165235007 A-to-I Human chr3 + 179393996 179393996 179393996 CTCCCACATCAGCCTCCTGGGTGGCTGGGACTACAGGCACACGCCACCATGCCTGGCTAGTTTTT CTCCCACATCAGCCTCCTGGGTGGCTGGGACTGCAGGCACACGCCACCATGCCTGGCTAGTTTTT A G MFN1 Ensembl:ENSG00000171109 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1373010618 Functional Loss SNV dbSNP153 33..33 33 - - - 25114 RMVar_ID_25114 Human_SNP_ID_165235025 A-to-I Human chr3 + 179394048 179394048 179394048 CTGGCTAGTTTTTGTAAAGACGAGGTTTCCCCATGTTGTGCAGGCTGGTCTTGAACTCACAGACT CTGGCTAGTTTTTGTAAAGACGAGGTTTCCCCCTGTTGTGCAGGCTGGTCTTGAACTCACAGACT A C MFN1 Ensembl:ENSG00000171109 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335839953 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14736496 25115 RMVar_ID_25115 Human_SNP_ID_165235068 A-to-I Human chr3 - 179394175 179394173 179394175 CCATAGGTCTGGGTTCAGACCCAAGGATCCACACTTTTTATAAGTTTGAAGGTTGATTATAGCTG CCATAGGTCTGGGTTCAGACCCAAGGATCCAC__TTTTTATAAGTTTGAAGGTTGATTATAGCTG AGT A - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1331938291 Functional Loss DEL dbSNP153 33..34 33 - - - 25116 RMVar_ID_25116 Human_SNP_ID_165235069 A-to-I Human chr3 - 179394175 179394175 179394175 CCATAGGTCTGGGTTCAGACCCAAGGATCCACACTTTTTATAAGTTTGAAGGTTGATTATAGCTG CCATAGGTCTGGGTTCAGACCCAAGGATCCACGCTTTTTATAAGTTTGAAGGTTGATTATAGCTG T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs532329233 Functional Loss SNV dbSNP153 33..33 33 - - - 25117 RMVar_ID_25117 Human_SNP_ID_165236217 A-to-I Human chr3 - 179397623 179397623 179397623 ATATCCAAGGTTCCTCCCTAGCTCAAGTTTTTACTTGTGATTACACACACCACATTGAATTCCGT ATATCCAAGGTTCCTCCCTAGCTCAAGTTTTTGCTTGTGATTACACACACCACATTGAATTCCGT T C GNB4 Ensembl:ENSG00000114450 Protein coding 3'UTR GSE100210;GSE112787 HepG2 cell line;293 Flip-In T-REx cells,empty vector - 29129909,29967493 RNA-Seq:(High) rs11539414 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14736521,Human_RBP_ID_26824244 Human_miRNA_ID_2779174 RMVar_hsa_circ_105486,RMVar_hsa_circ_117926,RMVar_hsa_circ_128128,RMVar_hsa_circ_110542,RMVar_hsa_circ_222912,RMVar_hsa_circ_89333,RMVar_hsa_circ_94368,RMVar_hsa_circ_222914,RMVar_hsa_circ_85129,RMVar_hsa_circ_222915,RMVar_hsa_circ_222913,RMVar_hsa_circ_222910,RMVar_hsa_circ_222911,RMVar_hsa_circ_222909 25118 RMVar_ID_25118 Human_SNP_ID_165236248 A-to-I Human chr3 - 179397767 179397767 179397767 GCGCCACTGCACTCCAACCCGAGCGACAGAGCAAGATTCCGTCCCAAAAAGAAAAAGCAGTTTTT GCGCCACTGCACTCCAACCCGAGCGACAGAGCGAGATTCCGTCCCAAAAAGAAAAAGCAGTTTTT T C GNB4 Ensembl:ENSG00000114450 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs11539415 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23188782,Human_RBP_ID_26510643 RMVar_hsa_circ_105486,RMVar_hsa_circ_117926,RMVar_hsa_circ_128128,RMVar_hsa_circ_110542,RMVar_hsa_circ_222912,RMVar_hsa_circ_89333,RMVar_hsa_circ_94368,RMVar_hsa_circ_222914,RMVar_hsa_circ_85129,RMVar_hsa_circ_222915,RMVar_hsa_circ_222913,RMVar_hsa_circ_222910,RMVar_hsa_circ_222911,RMVar_hsa_circ_222909 25119 RMVar_ID_25119 Human_SNP_ID_165236266 A-to-I Human chr3 - 179397829 179397827 179397829 CGTGAGGCTGAGGCAGAGAATTACTTGAACTCAGGAGGTGGAGGTTTTGGTGAGCTGAGATGGCG CGTGAGGCTGAGGCAGAGAATTACTTGAACTC__GAGGTGGAGGTTTTGGTGAGCTGAGATGGCG CCT C GNB4 Ensembl:ENSG00000114450 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1461800178 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_4731803,Human_RBP_ID_18000366,Human_RBP_ID_26505788 RMVar_hsa_circ_105486,RMVar_hsa_circ_117926,RMVar_hsa_circ_128128,RMVar_hsa_circ_110542,RMVar_hsa_circ_222912,RMVar_hsa_circ_89333,RMVar_hsa_circ_94368,RMVar_hsa_circ_222914,RMVar_hsa_circ_85129,RMVar_hsa_circ_222915,RMVar_hsa_circ_222913,RMVar_hsa_circ_222910,RMVar_hsa_circ_222911,RMVar_hsa_circ_222909 25120 RMVar_ID_25120 Human_SNP_ID_165236267 A-to-I Human chr3 - 179397834 179397834 179397834 CTACTCGTGAGGCTGAGGCAGAGAATTACTTGAACTCAGGAGGTGGAGGTTTTGGTGAGCTGAGA CTACTCGTGAGGCTGAGGCAGAGAATTACTTGCACTCAGGAGGTGGAGGTTTTGGTGAGCTGAGA T G GNB4 Ensembl:ENSG00000114450 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978484989 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18000366,Human_RBP_ID_26505788 RMVar_hsa_circ_105486,RMVar_hsa_circ_117926,RMVar_hsa_circ_128128,RMVar_hsa_circ_110542,RMVar_hsa_circ_222912,RMVar_hsa_circ_89333,RMVar_hsa_circ_94368,RMVar_hsa_circ_222914,RMVar_hsa_circ_85129,RMVar_hsa_circ_222915,RMVar_hsa_circ_222913,RMVar_hsa_circ_222910,RMVar_hsa_circ_222911,RMVar_hsa_circ_222909 25121 RMVar_ID_25121 Human_SNP_ID_165236271 A-to-I Human chr3 - 179397839 179397839 179397839 GTCAGCTACTCGTGAGGCTGAGGCAGAGAATTACTTGAACTCAGGAGGTGGAGGTTTTGGTGAGC GTCAGCTACTCGTGAGGCTGAGGCAGAGAATTGCTTGAACTCAGGAGGTGGAGGTTTTGGTGAGC T C GNB4 Ensembl:ENSG00000114450 Protein coding 3'UTR GSE47997;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,29129909,29796672,31158229,31158229,31158229 RNA-Seq:(High) rs1228174751 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18000366,Human_RBP_ID_26505788 RMVar_hsa_circ_105486,RMVar_hsa_circ_117926,RMVar_hsa_circ_128128,RMVar_hsa_circ_110542,RMVar_hsa_circ_222912,RMVar_hsa_circ_89333,RMVar_hsa_circ_94368,RMVar_hsa_circ_222914,RMVar_hsa_circ_85129,RMVar_hsa_circ_222915,RMVar_hsa_circ_222913,RMVar_hsa_circ_222910,RMVar_hsa_circ_222911,RMVar_hsa_circ_222909 25122 RMVar_ID_25122 Human_SNP_ID_165236272 A-to-I Human chr3 - 179397842 179397841 179397842 CCTGTCAGCTACTCGTGAGGCTGAGGCAGAGAATTACTTGAACTCAGGAGGTGGAGGTTTTGGTG CCTGTCAGCTACTCGTGAGGCTGAGGCAGAGA_TTACTTGAACTCAGGAGGTGGAGGTTTTGGTG AT A GNB4 Ensembl:ENSG00000114450 Protein coding 3'UTR GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs147984080 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_18000366,Human_RBP_ID_26505788 RMVar_hsa_circ_105486,RMVar_hsa_circ_117926,RMVar_hsa_circ_128128,RMVar_hsa_circ_110542,RMVar_hsa_circ_222912,RMVar_hsa_circ_89333,RMVar_hsa_circ_94368,RMVar_hsa_circ_222914,RMVar_hsa_circ_85129,RMVar_hsa_circ_222915,RMVar_hsa_circ_222913,RMVar_hsa_circ_222910,RMVar_hsa_circ_222911,RMVar_hsa_circ_222909 25123 RMVar_ID_25123 Human_SNP_ID_165236273 A-to-I Human chr3 - 179397842 179397842 179397842 CCTGTCAGCTACTCGTGAGGCTGAGGCAGAGAATTACTTGAACTCAGGAGGTGGAGGTTTTGGTG CCTGTCAGCTACTCGTGAGGCTGAGGCAGAGAGTTACTTGAACTCAGGAGGTGGAGGTTTTGGTG T C GNB4 Ensembl:ENSG00000114450 Protein coding 3'UTR GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs3180284 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18000366,Human_RBP_ID_26505788 RMVar_hsa_circ_105486,RMVar_hsa_circ_117926,RMVar_hsa_circ_128128,RMVar_hsa_circ_110542,RMVar_hsa_circ_222912,RMVar_hsa_circ_89333,RMVar_hsa_circ_94368,RMVar_hsa_circ_222914,RMVar_hsa_circ_85129,RMVar_hsa_circ_222915,RMVar_hsa_circ_222913,RMVar_hsa_circ_222910,RMVar_hsa_circ_222911,RMVar_hsa_circ_222909 25124 RMVar_ID_25124 Human_SNP_ID_165236274 A-to-I Human chr3 - 179397847 179397847 179397847 GGGCGCCTGTCAGCTACTCGTGAGGCTGAGGCAGAGAATTACTTGAACTCAGGAGGTGGAGGTTT GGGCGCCTGTCAGCTACTCGTGAGGCTGAGGCGGAGAATTACTTGAACTCAGGAGGTGGAGGTTT T C GNB4 Ensembl:ENSG00000114450 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs3180283 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26505788 RMVar_hsa_circ_105486,RMVar_hsa_circ_117926,RMVar_hsa_circ_128128,RMVar_hsa_circ_110542,RMVar_hsa_circ_222912,RMVar_hsa_circ_89333,RMVar_hsa_circ_94368,RMVar_hsa_circ_222914,RMVar_hsa_circ_85129,RMVar_hsa_circ_222915,RMVar_hsa_circ_222913,RMVar_hsa_circ_222910,RMVar_hsa_circ_222911,RMVar_hsa_circ_222909 25125 RMVar_ID_25125 Human_SNP_ID_165236280 A-to-I Human chr3 - 179397868 179397868 179397868 AAATTAGCCGGGCGTGGAGGTGGGCGCCTGTCAGCTACTCGTGAGGCTGAGGCAGAGAATTACTT AAATTAGCCGGGCGTGGAGGTGGGCGCCTGTCGGCTACTCGTGAGGCTGAGGCAGAGAATTACTT T C GNB4 Ensembl:ENSG00000114450 Protein coding 3'UTR GSE100210;GSE107867 HepG2 cell line;ASD brains,temporal_cortex - 29129909,30559470 RNA-Seq:(High) rs1373295202 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26511416 RMVar_hsa_circ_105486,RMVar_hsa_circ_117926,RMVar_hsa_circ_128128,RMVar_hsa_circ_110542,RMVar_hsa_circ_222912,RMVar_hsa_circ_89333,RMVar_hsa_circ_94368,RMVar_hsa_circ_222914,RMVar_hsa_circ_85129,RMVar_hsa_circ_222915,RMVar_hsa_circ_222913,RMVar_hsa_circ_222910,RMVar_hsa_circ_222911,RMVar_hsa_circ_222909 25126 RMVar_ID_25126 Human_SNP_ID_165236293 A-to-I Human chr3 - 179397901 179397901 179397901 GATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCCGGGCGTGGAGGTGGGCGCCTGTC GATGGTGAAACCCCATCTCTACTAAAAATACACAAATTAGCCGGGCGTGGAGGTGGGCGCCTGTC T G GNB4 Ensembl:ENSG00000114450 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs952752388 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105486,RMVar_hsa_circ_117926,RMVar_hsa_circ_128128,RMVar_hsa_circ_110542,RMVar_hsa_circ_222912,RMVar_hsa_circ_89333,RMVar_hsa_circ_94368,RMVar_hsa_circ_222914,RMVar_hsa_circ_85129,RMVar_hsa_circ_222915,RMVar_hsa_circ_222913,RMVar_hsa_circ_222910,RMVar_hsa_circ_222911,RMVar_hsa_circ_222909 25127 RMVar_ID_25127 Human_SNP_ID_165236294 A-to-I Human chr3 - 179397902 179397902 179397902 AGATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCCGGGCGTGGAGGTGGGCGCCTGT AGATGGTGAAACCCCATCTCTACTAAAAATACGAAAATTAGCCGGGCGTGGAGGTGGGCGCCTGT T C GNB4 Ensembl:ENSG00000114450 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1182836692 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105486,RMVar_hsa_circ_117926,RMVar_hsa_circ_128128,RMVar_hsa_circ_110542,RMVar_hsa_circ_222912,RMVar_hsa_circ_89333,RMVar_hsa_circ_94368,RMVar_hsa_circ_222914,RMVar_hsa_circ_85129,RMVar_hsa_circ_222915,RMVar_hsa_circ_222913,RMVar_hsa_circ_222910,RMVar_hsa_circ_222911,RMVar_hsa_circ_222909 25128 RMVar_ID_25128 Human_SNP_ID_165236297 A-to-I Human chr3 - 179397909 179397909 179397909 CTGGCCAAGATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCCGGGCGTGGAGGTGGG CTGGCCAAGATGGTGAAACCCCATCTCTACTACAAATACAAAAATTAGCCGGGCGTGGAGGTGGG T G GNB4 Ensembl:ENSG00000114450 Protein coding 3'UTR GSE47997;GSE99789;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;esophageal squamous carcinoma cells,EC109;ASD brains,frontal_cortex;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 23474544,29796672,30559470,31158229,31158229 RNA-Seq:(High) rs1392658431 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105486,RMVar_hsa_circ_117926,RMVar_hsa_circ_128128,RMVar_hsa_circ_110542,RMVar_hsa_circ_222912,RMVar_hsa_circ_89333,RMVar_hsa_circ_94368,RMVar_hsa_circ_222914,RMVar_hsa_circ_85129,RMVar_hsa_circ_222915,RMVar_hsa_circ_222913,RMVar_hsa_circ_222910,RMVar_hsa_circ_222911,RMVar_hsa_circ_222909 25129 RMVar_ID_25129 Human_SNP_ID_165236298 A-to-I Human chr3 - 179397910 179397910 179397910 CCTGGCCAAGATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCCGGGCGTGGAGGTGG CCTGGCCAAGATGGTGAAACCCCATCTCTACTGAAAATACAAAAATTAGCCGGGCGTGGAGGTGG T C GNB4 Ensembl:ENSG00000114450 Protein coding 3'UTR GSE47997;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,29129909,29796672,31158229,31158229,31158229 RNA-Seq:(High) rs985493465 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105486,RMVar_hsa_circ_117926,RMVar_hsa_circ_128128,RMVar_hsa_circ_110542,RMVar_hsa_circ_222912,RMVar_hsa_circ_89333,RMVar_hsa_circ_94368,RMVar_hsa_circ_222914,RMVar_hsa_circ_85129,RMVar_hsa_circ_222915,RMVar_hsa_circ_222913,RMVar_hsa_circ_222910,RMVar_hsa_circ_222911,RMVar_hsa_circ_222909 25130 RMVar_ID_25130 Human_SNP_ID_165236299 A-to-I Human chr3 - 179397913 179397913 179397913 CAGCCTGGCCAAGATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCCGGGCGTGGAGG CAGCCTGGCCAAGATGGTGAAACCCCATCTCTGCTAAAAATACAAAAATTAGCCGGGCGTGGAGG T C GNB4 Ensembl:ENSG00000114450 Protein coding 3'UTR GSE47997;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,29129909,29796672,31158229,31158229,31158229 RNA-Seq:(High) rs1396653078 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105486,RMVar_hsa_circ_117926,RMVar_hsa_circ_128128,RMVar_hsa_circ_110542,RMVar_hsa_circ_222912,RMVar_hsa_circ_89333,RMVar_hsa_circ_94368,RMVar_hsa_circ_222914,RMVar_hsa_circ_85129,RMVar_hsa_circ_222915,RMVar_hsa_circ_222913,RMVar_hsa_circ_222910,RMVar_hsa_circ_222911,RMVar_hsa_circ_222909 25131 RMVar_ID_25131 Human_SNP_ID_165236304 A-to-I Human chr3 - 179397934 179397934 179397934 ACGAGGTCAGGAGTTCAAGACCAGCCTGGCCAAGATGGTGAAACCCCATCTCTACTAAAAATACA ACGAGGTCAGGAGTTCAAGACCAGCCTGGCCAGGATGGTGAAACCCCATCTCTACTAAAAATACA T C GNB4 Ensembl:ENSG00000114450 Protein coding 3'UTR GSE47997;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829 K562 cells&HepG2 cells;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line - 23474544,29796672,31158229 RNA-Seq:(High) rs1427496211 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105486,RMVar_hsa_circ_117926,RMVar_hsa_circ_128128,RMVar_hsa_circ_110542,RMVar_hsa_circ_222912,RMVar_hsa_circ_89333,RMVar_hsa_circ_94368,RMVar_hsa_circ_222914,RMVar_hsa_circ_85129,RMVar_hsa_circ_222915,RMVar_hsa_circ_222913,RMVar_hsa_circ_222910,RMVar_hsa_circ_222911,RMVar_hsa_circ_222909 25132 RMVar_ID_25132 Human_SNP_ID_165236319 A-to-I Human chr3 - 179398001 179398001 179398001 TTCTTGGCCAGGCATGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGTGGA TTCTTGGCCAGGCATGGTGGCTCACACCTGTAGTCCCAGCACTTTGGGAGGCCGAGGCAGGTGGA T C GNB4 Ensembl:ENSG00000114450 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs12630273 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_154443 RMVar_hsa_circ_105486,RMVar_hsa_circ_117926,RMVar_hsa_circ_128128,RMVar_hsa_circ_110542,RMVar_hsa_circ_222912,RMVar_hsa_circ_89333,RMVar_hsa_circ_94368,RMVar_hsa_circ_222914,RMVar_hsa_circ_85129,RMVar_hsa_circ_222915,RMVar_hsa_circ_222913,RMVar_hsa_circ_222910,RMVar_hsa_circ_222911,RMVar_hsa_circ_222909 25133 RMVar_ID_25133 Human_SNP_ID_165236322 A-to-I Human chr3 - 179398010 179398010 179398010 AGCAAGCAGTTCTTGGCCAGGCATGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAG AGCAAGCAGTTCTTGGCCAGGCATGGTGGCTCCCACCTGTAATCCCAGCACTTTGGGAGGCCGAG T G GNB4 Ensembl:ENSG00000114450 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1356215956 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7162651 RMVar_hsa_circ_105486,RMVar_hsa_circ_117926,RMVar_hsa_circ_128128,RMVar_hsa_circ_110542,RMVar_hsa_circ_222912,RMVar_hsa_circ_89333,RMVar_hsa_circ_94368,RMVar_hsa_circ_222914,RMVar_hsa_circ_85129,RMVar_hsa_circ_222915,RMVar_hsa_circ_222913,RMVar_hsa_circ_222910,RMVar_hsa_circ_222911,RMVar_hsa_circ_222909 25134 RMVar_ID_25134 Human_SNP_ID_165236393 A-to-I Human chr3 - 179398270 179398270 179398270 CCTCAAGTGATCCACCAGCCTCAGCCTCCCAAAGTGCTGGGATTACAGACGTGAGCCACCGTGCC CCTCAAGTGATCCACCAGCCTCAGCCTCCCAAGGTGCTGGGATTACAGACGTGAGCCACCGTGCC T C GNB4 Ensembl:ENSG00000114450 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1318437029 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105486,RMVar_hsa_circ_117926,RMVar_hsa_circ_128128,RMVar_hsa_circ_110542,RMVar_hsa_circ_222912,RMVar_hsa_circ_89333,RMVar_hsa_circ_94368,RMVar_hsa_circ_222914,RMVar_hsa_circ_85129,RMVar_hsa_circ_222915,RMVar_hsa_circ_222913,RMVar_hsa_circ_222910,RMVar_hsa_circ_222911,RMVar_hsa_circ_222909 25135 RMVar_ID_25135 Human_SNP_ID_165236399 A-to-I Human chr3 - 179398289 179398289 179398289 TCTGATCTCGTACTCCTGGCCTCAAGTGATCCACCAGCCTCAGCCTCCCAAAGTGCTGGGATTAC TCTGATCTCGTACTCCTGGCCTCAAGTGATCCCCCAGCCTCAGCCTCCCAAAGTGCTGGGATTAC T G GNB4 Ensembl:ENSG00000114450 Protein coding 3'UTR GSE100210;GSE99789;GSE123020:GSM3490829,GSM3490830,GSM3490831 HepG2 cell line;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109 cell line - 29129909,29796672,32596459 RNA-Seq:(High) rs1358483004 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105486,RMVar_hsa_circ_117926,RMVar_hsa_circ_128128,RMVar_hsa_circ_110542,RMVar_hsa_circ_222912,RMVar_hsa_circ_89333,RMVar_hsa_circ_94368,RMVar_hsa_circ_222914,RMVar_hsa_circ_85129,RMVar_hsa_circ_222915,RMVar_hsa_circ_222913,RMVar_hsa_circ_222910,RMVar_hsa_circ_222911,RMVar_hsa_circ_222909 25136 RMVar_ID_25136 Human_SNP_ID_165236402 A-to-I Human chr3 - 179398297 179398297 179398297 TTGGCCAGTCTGATCTCGTACTCCTGGCCTCAAGTGATCCACCAGCCTCAGCCTCCCAAAGTGCT TTGGCCAGTCTGATCTCGTACTCCTGGCCTCAGGTGATCCACCAGCCTCAGCCTCCCAAAGTGCT T C GNB4 Ensembl:ENSG00000114450 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886443501 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105486,RMVar_hsa_circ_117926,RMVar_hsa_circ_128128,RMVar_hsa_circ_110542,RMVar_hsa_circ_222912,RMVar_hsa_circ_89333,RMVar_hsa_circ_94368,RMVar_hsa_circ_222914,RMVar_hsa_circ_85129,RMVar_hsa_circ_222915,RMVar_hsa_circ_222913,RMVar_hsa_circ_222910,RMVar_hsa_circ_222911,RMVar_hsa_circ_222909 25137 RMVar_ID_25137 Human_SNP_ID_165236405 A-to-I Human chr3 - 179398310 179398310 179398310 GGGTTTCACCATCTTGGCCAGTCTGATCTCGTACTCCTGGCCTCAAGTGATCCACCAGCCTCAGC GGGTTTCACCATCTTGGCCAGTCTGATCTCGTGCTCCTGGCCTCAAGTGATCCACCAGCCTCAGC T C GNB4 Ensembl:ENSG00000114450 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs944774511 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105486,RMVar_hsa_circ_117926,RMVar_hsa_circ_128128,RMVar_hsa_circ_110542,RMVar_hsa_circ_222912,RMVar_hsa_circ_89333,RMVar_hsa_circ_94368,RMVar_hsa_circ_222914,RMVar_hsa_circ_85129,RMVar_hsa_circ_222915,RMVar_hsa_circ_222913,RMVar_hsa_circ_222910,RMVar_hsa_circ_222911,RMVar_hsa_circ_222909 25138 RMVar_ID_25138 Human_SNP_ID_165236415 A-to-I Human chr3 - 179398335 179398335 179398335 AATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATCTTGGCCAGTCTGATCTCGTACTCCTGG AATTTTTGTATTTTTAGTAGAGATGGGGTTTCGCCATCTTGGCCAGTCTGATCTCGTACTCCTGG T C GNB4 Ensembl:ENSG00000114450 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1341188301 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105486,RMVar_hsa_circ_117926,RMVar_hsa_circ_128128,RMVar_hsa_circ_110542,RMVar_hsa_circ_222912,RMVar_hsa_circ_89333,RMVar_hsa_circ_94368,RMVar_hsa_circ_222914,RMVar_hsa_circ_85129,RMVar_hsa_circ_222915,RMVar_hsa_circ_222913,RMVar_hsa_circ_222910,RMVar_hsa_circ_222911,RMVar_hsa_circ_222909 25139 RMVar_ID_25139 Human_SNP_ID_165236417 A-to-I Human chr3 - 179398345 179398345 179398345 ATGCCCGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATCTTGGCCAGTCTGATCTC ATGCCCGGCTAATTTTTGTATTTTTAGTAGAGGTGGGGTTTCACCATCTTGGCCAGTCTGATCTC T C GNB4 Ensembl:ENSG00000114450 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1028229793 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105486,RMVar_hsa_circ_117926,RMVar_hsa_circ_128128,RMVar_hsa_circ_110542,RMVar_hsa_circ_222912,RMVar_hsa_circ_89333,RMVar_hsa_circ_94368,RMVar_hsa_circ_222914,RMVar_hsa_circ_85129,RMVar_hsa_circ_222915,RMVar_hsa_circ_222913,RMVar_hsa_circ_222910,RMVar_hsa_circ_222911,RMVar_hsa_circ_222909 25140 RMVar_ID_25140 Human_SNP_ID_165236434 A-to-I Human chr3 - 179398429 179398429 179398429 GCAACCTCAACCTCTGCCTCCTGGGTTCAAGCAATTCTTGTGCCTCAGCCTCCCAAGTAGCTGGG GCAACCTCAACCTCTGCCTCCTGGGTTCAAGCGATTCTTGTGCCTCAGCCTCCCAAGTAGCTGGG T C GNB4 Ensembl:ENSG00000114450 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1234154660 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105486,RMVar_hsa_circ_117926,RMVar_hsa_circ_128128,RMVar_hsa_circ_110542,RMVar_hsa_circ_222912,RMVar_hsa_circ_89333,RMVar_hsa_circ_94368,RMVar_hsa_circ_222914,RMVar_hsa_circ_85129,RMVar_hsa_circ_222915,RMVar_hsa_circ_222913,RMVar_hsa_circ_222910,RMVar_hsa_circ_222911,RMVar_hsa_circ_222909 25141 RMVar_ID_25141 Human_SNP_ID_165236569 A-to-I Human chr3 - 179398949 179398949 179398949 GTAGTCACAGGCATACAGACCACAGGAATTCTATGGTCTTAACATATTTTAAAATTACATTTATT GTAGTCACAGGCATACAGACCACAGGAATTCTGTGGTCTTAACATATTTTAAAATTACATTTATT T C GNB4 Ensembl:ENSG00000114450 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1163764246 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_595569,Human_RBP_ID_7162661,Human_RBP_ID_9136436,Human_RBP_ID_17518548,Human_RBP_ID_26510645 RMVar_hsa_circ_105486,RMVar_hsa_circ_117926,RMVar_hsa_circ_128128,RMVar_hsa_circ_110542,RMVar_hsa_circ_222912,RMVar_hsa_circ_89333,RMVar_hsa_circ_94368,RMVar_hsa_circ_222914,RMVar_hsa_circ_85129,RMVar_hsa_circ_222915,RMVar_hsa_circ_222913,RMVar_hsa_circ_222910,RMVar_hsa_circ_222911,RMVar_hsa_circ_222909 25142 RMVar_ID_25142 Human_SNP_ID_165236673 A-to-I Human chr3 - 179399324 179399324 179399324 GTGGCACATTCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGATTCGCCTGAACCCGGGA GTGGCACATTCCTGTAATCCCAGCTACTCGGGTGGCTGAGGCAGGAGATTCGCCTGAACCCGGGA T A GNB4 Ensembl:ENSG00000114450 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1205651742 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105486,RMVar_hsa_circ_117926,RMVar_hsa_circ_128128,RMVar_hsa_circ_110542,RMVar_hsa_circ_222912,RMVar_hsa_circ_89333,RMVar_hsa_circ_94368,RMVar_hsa_circ_222914,RMVar_hsa_circ_85129,RMVar_hsa_circ_222915,RMVar_hsa_circ_222913,RMVar_hsa_circ_222910,RMVar_hsa_circ_222911,RMVar_hsa_circ_222909 25143 RMVar_ID_25143 Human_SNP_ID_165236678 A-to-I Human chr3 - 179399331 179399331 179399331 GGGCGTGGTGGCACATTCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGATTCGCCTGAA GGGCGTGGTGGCACATTCCTGTAATCCCAGCTGCTCGGGAGGCTGAGGCAGGAGATTCGCCTGAA T C GNB4 Ensembl:ENSG00000114450 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1189892856 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105486,RMVar_hsa_circ_117926,RMVar_hsa_circ_128128,RMVar_hsa_circ_110542,RMVar_hsa_circ_222912,RMVar_hsa_circ_89333,RMVar_hsa_circ_94368,RMVar_hsa_circ_222914,RMVar_hsa_circ_85129,RMVar_hsa_circ_222915,RMVar_hsa_circ_222913,RMVar_hsa_circ_222910,RMVar_hsa_circ_222911,RMVar_hsa_circ_222909 25144 RMVar_ID_25144 Human_SNP_ID_165236680 A-to-I Human chr3 - 179399340 179399340 179399340 ACATTAGCCGGGCGTGGTGGCACATTCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAT ACATTAGCCGGGCGTGGTGGCACATTCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAT T C GNB4 Ensembl:ENSG00000114450 Protein coding 3'UTR GSE100210;GSE99789;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;esophageal squamous carcinoma cells,EC109;ASD brains,Fragile X samples from NIH NeuroBioBank;Bronchiolar epithelium,BEP2D cell line - 29129909,29796672,30559470,31158229 RNA-Seq:(High) rs1472458895 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105486,RMVar_hsa_circ_117926,RMVar_hsa_circ_128128,RMVar_hsa_circ_110542,RMVar_hsa_circ_222912,RMVar_hsa_circ_89333,RMVar_hsa_circ_94368,RMVar_hsa_circ_222914,RMVar_hsa_circ_85129,RMVar_hsa_circ_222915,RMVar_hsa_circ_222913,RMVar_hsa_circ_222910,RMVar_hsa_circ_222911,RMVar_hsa_circ_222909 25145 RMVar_ID_25145 Human_SNP_ID_165236689 A-to-I Human chr3 - 179399376 179399376 179399376 CAACATGGTGAAACCCCATCTCTTCTAAAAATACAAACATTAGCCGGGCGTGGTGGCACATTCCT CAACATGGTGAAACCCCATCTCTTCTAAAAATCCAAACATTAGCCGGGCGTGGTGGCACATTCCT T G GNB4 Ensembl:ENSG00000114450 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs199714419 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14736533 RMVar_hsa_circ_105486,RMVar_hsa_circ_117926,RMVar_hsa_circ_128128,RMVar_hsa_circ_110542,RMVar_hsa_circ_222912,RMVar_hsa_circ_89333,RMVar_hsa_circ_94368,RMVar_hsa_circ_222914,RMVar_hsa_circ_85129,RMVar_hsa_circ_222915,RMVar_hsa_circ_222913,RMVar_hsa_circ_222910,RMVar_hsa_circ_222911,RMVar_hsa_circ_222909 25146 RMVar_ID_25146 Human_SNP_ID_165236721 A-to-I Human chr3 - 179399484 179399484 179399484 TCTATTAACTTTTTGGCTGGGCAGAGTGGCTTACACCTATAATCCCAGCAATTTGGGAGGCCAAG TCTATTAACTTTTTGGCTGGGCAGAGTGGCTTTCACCTATAATCCCAGCAATTTGGGAGGCCAAG T A GNB4 Ensembl:ENSG00000114450 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1159424294 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8210803,Human_RBP_ID_26510647 Human_miRNA_ID_1359674 RMVar_hsa_circ_105486,RMVar_hsa_circ_117926,RMVar_hsa_circ_128128,RMVar_hsa_circ_110542,RMVar_hsa_circ_222912,RMVar_hsa_circ_89333,RMVar_hsa_circ_94368,RMVar_hsa_circ_222914,RMVar_hsa_circ_85129,RMVar_hsa_circ_222915,RMVar_hsa_circ_222913,RMVar_hsa_circ_222910,RMVar_hsa_circ_222911,RMVar_hsa_circ_222909 25147 RMVar_ID_25147 Human_SNP_ID_165236857 A-to-I Human chr3 - 179400020 179400020 179400020 AAAGGATGTCTAGATGTAAGTGATTCCACTTAAAGCCAAAATAAAAATTCCTAAAGCAGTTCTTA AAAGGATGTCTAGATGTAAGTGATTCCACTTAGAGCCAAAATAAAAATTCCTAAAGCAGTTCTTA T C GNB4 Ensembl:ENSG00000114450 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs915964802 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_595587 RMVar_hsa_circ_105486,RMVar_hsa_circ_117926,RMVar_hsa_circ_128128,RMVar_hsa_circ_110542,RMVar_hsa_circ_222912,RMVar_hsa_circ_89333,RMVar_hsa_circ_94368,RMVar_hsa_circ_222914,RMVar_hsa_circ_85129,RMVar_hsa_circ_222915,RMVar_hsa_circ_222913,RMVar_hsa_circ_222910,RMVar_hsa_circ_222911,RMVar_hsa_circ_222909 25148 RMVar_ID_25148 Human_SNP_ID_165247991 A-to-I Human chr3 - 179445347 179445347 179445347 GCAAGAGGCAGAGGTTGCAGTGAACTATGATCATGCCACTGCACTCCAGCCTGGGTGACAGAGGA GCAAGAGGCAGAGGTTGCAGTGAACTATGATCGTGCCACTGCACTCCAGCCTGGGTGACAGAGGA T C GNB4 Ensembl:ENSG00000114450 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs993367491 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25717070 25149 RMVar_ID_25149 Human_SNP_ID_165280271 A-to-I Human chr3 + 179579641 179579641 179579641 GAGACCCCATCTCTACTAAAAATACAAAAATTAGCTGGGTTTGGTGCTGAGCACCTGTAATCCCA GAGACCCCATCTCTACTAAAAATACAAAAATTGGCTGGGTTTGGTGCTGAGCACCTGTAATCCCA A G ACTL6A Ensembl:ENSG00000136518 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1423418398 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_222928,RMVar_hsa_circ_329671,RMVar_hsa_circ_91423,RMVar_hsa_circ_55659,RMVar_hsa_circ_116499,RMVar_hsa_circ_222931 25150 RMVar_ID_25150 Human_SNP_ID_165282216 A-to-I Human chr3 + 179588199 179588196 179588199 AATTAAGTTTGTGCTTTCCTTGAAATGCACTTATTCTTATTACAAGCATTTTATAATTTTGTATA AATTAAGTTTGTGCTTTCCTTGAAATGCAC___TTCTTATTACAAGCATTTTATAATTTTGTATA CTTA C ACTL6A Ensembl:ENSG00000136518 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1443505135 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_595657,Human_RBP_ID_1032094,Human_RBP_ID_7245780,Human_RBP_ID_17518567,Human_RBP_ID_18335846,Human_RBP_ID_24496921,Human_RBP_ID_27715655 Human_miRNA_ID_2805206,Human_miRNA_ID_2808349,Human_miRNA_ID_2811492 RMVar_hsa_circ_222928,RMVar_hsa_circ_91423,RMVar_hsa_circ_116499,RMVar_hsa_circ_85526,RMVar_hsa_circ_222931,RMVar_hsa_circ_84242,RMVar_hsa_circ_222932,RMVar_hsa_circ_222933 25151 RMVar_ID_25151 Human_SNP_ID_165291628 A-to-I Human chr3 + 179625024 179625024 179625024 GTTGGCCAGGCTGGTCTTGAACTTCTGACCTCAGGTGATTGGCCTGTCTCCACTTCCCAAAGTGC GTTGGCCAGGCTGGTCTTGAACTTCTGACCTCGGGTGATTGGCCTGTCTCCACTTCCCAAAGTGC A G NDUFB5 Ensembl:ENSG00000136521 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893287750 Functional Loss SNV dbSNP153 33..33 33 - - - 25152 RMVar_ID_25152 Human_SNP_ID_93077172 A-to-I Human chr2 + 135067870 135067870 135067870 CTTCCACCTCAGCCTCCTGAGTAGCTGGGACTACAGGTACATGCCACCATGCCCAGCTAATTGGT CTTCCACCTCAGCCTCCTGAGTAGCTGGGACTGCAGGTACATGCCACCATGCCCAGCTAATTGGT A G RAB3GAP1 Ensembl:ENSG00000115839 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs975080752 Functional Loss SNV dbSNP153 33..33 33 - - - 25153 RMVar_ID_25153 Human_SNP_ID_93079063 A-to-I Human chr2 + 135076010 135076010 135076010 TCAGCTCACTGCAGCCTTCGCCTCCTGCGTTGAAGTGATTCTCCTGCCTCAGCCTCCTGAGTAGC TCAGCTCACTGCAGCCTTCGCCTCCTGCGTTGGAGTGATTCTCCTGCCTCAGCCTCCTGAGTAGC A G RAB3GAP1 Ensembl:ENSG00000115839 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1281501495 Functional Loss SNV dbSNP153 33..33 33 - - - 25154 RMVar_ID_25154 Human_SNP_ID_93079285 A-to-I Human chr2 + 135076998 135076998 135076998 CACATTTTAAAATCCATTCCTTGGCCAAGCACAGTGGCTCATGCCTGTAATCCCAGCACTTTGGG CACATTTTAAAATCCATTCCTTGGCCAAGCACGGTGGCTCATGCCTGTAATCCCAGCACTTTGGG A G RAB3GAP1 Ensembl:ENSG00000115839 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1191449542 Functional Loss SNV dbSNP153 33..33 33 - - - 25155 RMVar_ID_25155 Human_SNP_ID_93079321 A-to-I Human chr2 + 135077159 135077159 135077159 AGGCATGGTGGCTCACGCCTGTGGTCCTAGCTACTCGGGAGGCTGAGACAGGAGAATTGCTTGAA AGGCATGGTGGCTCACGCCTGTGGTCCTAGCTCCTCGGGAGGCTGAGACAGGAGAATTGCTTGAA A C RAB3GAP1 Ensembl:ENSG00000115839 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs945684385 Functional Loss SNV dbSNP153 33..33 33 - - - 25156 RMVar_ID_25156 Human_SNP_ID_93079397 A-to-I Human chr2 + 135077436 135077436 135077436 TGTGTAGGCTGGGCATGGTGGCTCATGCCTGTAATCCCAGCATTTTGGGAGGCCCAGGCAGGAAG TGTGTAGGCTGGGCATGGTGGCTCATGCCTGTCATCCCAGCATTTTGGGAGGCCCAGGCAGGAAG A C RAB3GAP1 Ensembl:ENSG00000115839 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1460859829 Functional Loss SNV dbSNP153 33..33 33 - - - 25157 RMVar_ID_25157 Human_SNP_ID_93094641 A-to-I Human chr2 + 135139272 135139272 135139272 AATAAAGTGTACAGATCTTGGCTGGGCATGGTAGCTCATGCCTGTAATCCCAGCACTTTGGGAGG AATAAAGTGTACAGATCTTGGCTGGGCATGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGG A G RAB3GAP1 Ensembl:ENSG00000115839 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947413037 Functional Loss SNV dbSNP153 33..33 33 - - - 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 25158 RMVar_ID_25158 Human_SNP_ID_93094668 A-to-I Human chr2 + 135139378 135139377 135139378 GCCTGAGGAACATGACAAAACCCCGTCTCTACAAAAAATACAGAAATTAGCCGAGCGTGGTGGTG GCCTGAGGAACATGACAAAACCCCGTCTCTAC_AAAAATACAGAAATTAGCCGAGCGTGGTGGTG CA C RAB3GAP1 Ensembl:ENSG00000115839 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1439903381 Functional Loss DEL dbSNP153 33..33 33 - - - 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 25159 RMVar_ID_25159 Human_SNP_ID_93134794 A-to-I Human chr2 - 135313319 135313319 135313319 GTTGGGAGCCTCACTCTGTCACCCTGGCTGGAATGCAGTGGCGTGATCTCGGCTCACTGCAGCCT GTTGGGAGCCTCACTCTGTCACCCTGGCTGGAGTGCAGTGGCGTGATCTCGGCTCACTGCAGCCT T C ZRANB3 Ensembl:ENSG00000121988 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs536154918 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41,RMVar_hsa_circ_203386,RMVar_hsa_circ_92458,RMVar_hsa_circ_51809,RMVar_hsa_circ_68612,RMVar_hsa_circ_74529,RMVar_hsa_circ_59490,RMVar_hsa_circ_304177,RMVar_hsa_circ_341740,RMVar_hsa_circ_15922,RMVar_hsa_circ_203394,RMVar_hsa_circ_266964 25160 RMVar_ID_25160 Human_SNP_ID_93169122 A-to-I Human chr2 - 135449882 135449882 135449882 ATGGTTGTCTTTGCCTATAGTCCCAGGTACTCAGGAGGCTGCAGCAGGAGGATTGCTTGAGTCTG ATGGTTGTCTTTGCCTATAGTCCCAGGTACTCGGGAGGCTGCAGCAGGAGGATTGCTTGAGTCTG T C ZRANB3 Ensembl:ENSG00000121988 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749557799 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569925 RMVar_hsa_circ_51519 25161 RMVar_ID_25161 Human_SNP_ID_93169123 A-to-I Human chr2 - 135449882 135449882 135449882 ATGGTTGTCTTTGCCTATAGTCCCAGGTACTCAGGAGGCTGCAGCAGGAGGATTGCTTGAGTCTG ATGGTTGTCTTTGCCTATAGTCCCAGGTACTCCGGAGGCTGCAGCAGGAGGATTGCTTGAGTCTG T G ZRANB3 Ensembl:ENSG00000121988 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749557799 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569925 RMVar_hsa_circ_51519 25162 RMVar_ID_25162 Human_SNP_ID_93184230 A-to-I Human chr2 + 135510728 135510728 135510728 AGCTCGAGTCTTCTTCTCTTCCACATTCAGACAGACCTCACCTCTGAACATGATGGGCCTGTTGC AGCTCGAGTCTTCTTCTCTTCCACATTCAGACGGACCTCACCTCTGAACATGATGGGCCTGTTGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1237162912 Functional Loss SNV dbSNP153 33..33 33 - - - 25163 RMVar_ID_25163 Human_SNP_ID_93184293 A-to-I Human chr2 - 135510951 135510951 135510951 TGAGGCTGGTGAGCAAGGTGACATTGAACCCCAAAGAGTGGTGAGACACCCTGACAGTCACCAAC TGAGGCTGGTGAGCAAGGTGACATTGAACCCCGAAGAGTGGTGAGACACCCTGACAGTCACCAAC T C G3BP1P1,ZRANB3 Ensembl:ENSG00000235651,Ensembl:ENSG00000121988 Pseudogene,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1276869691 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3641811 Human_miRNA_ID_1836972 RMVar_hsa_circ_203405 25164 RMVar_ID_25164 Human_SNP_ID_93184503 A-to-I Human chr2 + 135511776 135511776 135511776 GACATCACTTTCCTGTGGATTTCTTTCTGTCCATAAACTGCATCTGCTAGCTTTCTATTTGAATC GACATCACTTTCCTGTGGATTTCTTTCTGTCCGTAAACTGCATCTGCTAGCTTTCTATTTGAATC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1487677064 Functional Loss SNV dbSNP153 33..33 33 - - - 25165 RMVar_ID_25165 Human_SNP_ID_93184508 A-to-I Human chr2 + 135511792 135511792 135511792 GGATTTCTTTCTGTCCATAAACTGCATCTGCTAGCTTTCTATTTGAATCCAATCCCCCATGGACA GGATTTCTTTCTGTCCATAAACTGCATCTGCTGGCTTTCTATTTGAATCCAATCCCCCATGGACA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1231298692 Functional Loss SNV dbSNP153 33..33 33 - - - 25166 RMVar_ID_25166 Human_SNP_ID_93188298 A-to-I Human chr2 - 135527476 135527476 135527476 TGGCTCACTGCAACCTCTGCCAACTGGGTTCAAGTGATTCTCCTGTCTCAGCCTCCTGAGTAGCT TGGCTCACTGCAACCTCTGCCAACTGGGTTCAGGTGATTCTCCTGTCTCAGCCTCCTGAGTAGCT T C ZRANB3 Ensembl:ENSG00000121988 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1179154866 Functional Loss SNV dbSNP153 33..33 33 - - - 25167 RMVar_ID_25167 Human_SNP_ID_93188858 A-to-I Human chr2 - 135529788 135529788 135529788 AGTGGCAGACAGGCGCGGTGGCTCAGACCTGTAATCCTAGCACTTTGGGAGGCCGAGGCGGGAGG AGTGGCAGACAGGCGCGGTGGCTCAGACCTGTCATCCTAGCACTTTGGGAGGCCGAGGCGGGAGG T G ZRANB3 Ensembl:ENSG00000121988 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs13028747 Functional Loss SNV dbSNP153 33..33 33 - - - 25168 RMVar_ID_25168 Human_SNP_ID_93190386 A-to-I Human chr2 + 135535378 135535378 135535378 AAAATTAGTAGGGCGTGTTGGCGGGTGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGACA AAAATTAGTAGGGCGTGTTGGCGGGTGCCTGTTGTCCCAGCTACTCGGGAGGCTGAGGCAGGACA A T R3HDM1 Ensembl:ENSG00000048991 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1162498399 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_203406,RMVar_hsa_circ_97196 25169 RMVar_ID_25169 Human_SNP_ID_93192339 A-to-I Human chr2 + 135542787 135542787 135542787 ATGAGACGGCGTCTCACTCTGTAGCCCAGGCTAGAGTGCAGTGCTGCAGTCTTGGCTCACCACAA ATGAGACGGCGTCTCACTCTGTAGCCCAGGCTGGAGTGCAGTGCTGCAGTCTTGGCTCACCACAA A G R3HDM1 Ensembl:ENSG00000048991 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1435177934 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_203406,RMVar_hsa_circ_97196 25170 RMVar_ID_25170 Human_SNP_ID_93206767 A-to-I Human chr2 + 135605824 135605824 135605824 CTCCTGCCTCAGCCTCCCGAGTAGCTAGGACTACAGGCATGCACCCCCACACCCGGCTAATTTTT CTCCTGCCTCAGCCTCCCGAGTAGCTAGGACTGCAGGCATGCACCCCCACACCCGGCTAATTTTT A G R3HDM1 Ensembl:ENSG00000048991 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1162169157 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_203410,RMVar_hsa_circ_203406,RMVar_hsa_circ_97196,RMVar_hsa_circ_309589,RMVar_hsa_circ_313853,RMVar_hsa_circ_318605,RMVar_hsa_circ_333426,RMVar_hsa_circ_311992,RMVar_hsa_circ_285779,RMVar_hsa_circ_293100,RMVar_hsa_circ_285409,RMVar_hsa_circ_23186,RMVar_hsa_circ_50693,RMVar_hsa_circ_271425,RMVar_hsa_circ_49087,RMVar_hsa_circ_203414,RMVar_hsa_circ_203416,RMVar_hsa_circ_203417,RMVar_hsa_circ_203415,RMVar_hsa_circ_203412,RMVar_hsa_circ_203413,RMVar_hsa_circ_203411,RMVar_hsa_circ_203420,RMVar_hsa_circ_203408,RMVar_hsa_circ_203409,RMVar_hsa_circ_336698,RMVar_hsa_circ_338185,RMVar_hsa_circ_203421 25171 RMVar_ID_25171 Human_SNP_ID_93209496 A-to-I Human chr2 + 135618300 135618300 135618300 ATTCTGCCTCAGCCTGCCGAGTAGCTGGAATTATAGGCACCCGCCACCACGCCTGGCTAATTTTT ATTCTGCCTCAGCCTGCCGAGTAGCTGGAATTGTAGGCACCCGCCACCACGCCTGGCTAATTTTT A G R3HDM1 Ensembl:ENSG00000048991 Protein coding intron GSE38233;GSE107867 cultured B-cells;ASD brains,frontal_cortex - 24183664,30559470 RNA-Seq:(High) rs995902213 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_203410,RMVar_hsa_circ_203406,RMVar_hsa_circ_97196,RMVar_hsa_circ_309589,RMVar_hsa_circ_313853,RMVar_hsa_circ_333426,RMVar_hsa_circ_311992,RMVar_hsa_circ_285779,RMVar_hsa_circ_293100,RMVar_hsa_circ_285409,RMVar_hsa_circ_23186,RMVar_hsa_circ_50693,RMVar_hsa_circ_271425,RMVar_hsa_circ_49087,RMVar_hsa_circ_203414,RMVar_hsa_circ_203415,RMVar_hsa_circ_203412,RMVar_hsa_circ_203413,RMVar_hsa_circ_203411,RMVar_hsa_circ_53691,RMVar_hsa_circ_203408,RMVar_hsa_circ_203409,RMVar_hsa_circ_338185,RMVar_hsa_circ_330910,RMVar_hsa_circ_375158,RMVar_hsa_circ_379103,RMVar_hsa_circ_353778,RMVar_hsa_circ_203428,RMVar_hsa_circ_1826,RMVar_hsa_circ_203426,RMVar_hsa_circ_338516,RMVar_hsa_circ_372987,RMVar_hsa_circ_110563,RMVar_hsa_circ_203429,RMVar_hsa_circ_203427 25172 RMVar_ID_25172 Human_SNP_ID_93212247 A-to-I Human chr2 + 135630183 135630183 135630183 CCTGTAGTCCCAGCTAATCGGGAGGCTGAGGCAGGAGAATTGCTTGAACCTGAGAGGCGGAGGTA CCTGTAGTCCCAGCTAATCGGGAGGCTGAGGCGGGAGAATTGCTTGAACCTGAGAGGCGGAGGTA A G R3HDM1 Ensembl:ENSG00000048991 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1340848581 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_131,RMVar_hsa_circ_203410,RMVar_hsa_circ_203406,RMVar_hsa_circ_97196,RMVar_hsa_circ_309589,RMVar_hsa_circ_313853,RMVar_hsa_circ_333426,RMVar_hsa_circ_311992,RMVar_hsa_circ_293100,RMVar_hsa_circ_23186,RMVar_hsa_circ_50693,RMVar_hsa_circ_271425,RMVar_hsa_circ_49087,RMVar_hsa_circ_203412,RMVar_hsa_circ_203413,RMVar_hsa_circ_203411,RMVar_hsa_circ_203408,RMVar_hsa_circ_203409,RMVar_hsa_circ_375158,RMVar_hsa_circ_379103,RMVar_hsa_circ_353778,RMVar_hsa_circ_203428,RMVar_hsa_circ_1826,RMVar_hsa_circ_203426,RMVar_hsa_circ_338516,RMVar_hsa_circ_110563,RMVar_hsa_circ_203429,RMVar_hsa_circ_312080,RMVar_hsa_circ_328939,RMVar_hsa_circ_358334,RMVar_hsa_circ_320654,RMVar_hsa_circ_81201,RMVar_hsa_circ_297511,RMVar_hsa_circ_34570,RMVar_hsa_circ_40475,RMVar_hsa_circ_53785,RMVar_hsa_circ_203431,RMVar_hsa_circ_203432,RMVar_hsa_circ_203430,RMVar_hsa_circ_50419 25173 RMVar_ID_25173 Human_SNP_ID_93215881 A-to-I Human chr2 + 135646586 135646586 135646586 AGAAGTATGATGGGCCTGGCGCGTTGGCTCACACCTGTAATCCCAGCACTTTAGGAGGCCGAGGC AGAAGTATGATGGGCCTGGCGCGTTGGCTCACGCCTGTAATCCCAGCACTTTAGGAGGCCGAGGC A G R3HDM1 Ensembl:ENSG00000048991 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs961277833 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_131,RMVar_hsa_circ_203406,RMVar_hsa_circ_97196,RMVar_hsa_circ_309589,RMVar_hsa_circ_313853,RMVar_hsa_circ_333426,RMVar_hsa_circ_50693,RMVar_hsa_circ_203408,RMVar_hsa_circ_203409,RMVar_hsa_circ_375158,RMVar_hsa_circ_379103,RMVar_hsa_circ_353778,RMVar_hsa_circ_203426,RMVar_hsa_circ_320654,RMVar_hsa_circ_81201,RMVar_hsa_circ_297511,RMVar_hsa_circ_34570,RMVar_hsa_circ_53785,RMVar_hsa_circ_203431,RMVar_hsa_circ_203432,RMVar_hsa_circ_203430,RMVar_hsa_circ_283944,RMVar_hsa_circ_284866,RMVar_hsa_circ_336992,RMVar_hsa_circ_203437,RMVar_hsa_circ_203434,RMVar_hsa_circ_203435,RMVar_hsa_circ_365020,RMVar_hsa_circ_375962,RMVar_hsa_circ_58079,RMVar_hsa_circ_203438,RMVar_hsa_circ_60843,RMVar_hsa_circ_59232,RMVar_hsa_circ_126534,RMVar_hsa_circ_108309,RMVar_hsa_circ_203439,RMVar_hsa_circ_203441,RMVar_hsa_circ_112928,RMVar_hsa_circ_203442,RMVar_hsa_circ_373448,RMVar_hsa_circ_311528,RMVar_hsa_circ_340970,RMVar_hsa_circ_203443,RMVar_hsa_circ_320581,RMVar_hsa_circ_305680,RMVar_hsa_circ_203445,RMVar_hsa_circ_203447,RMVar_hsa_circ_13702,RMVar_hsa_circ_203446,RMVar_hsa_circ_203444 25174 RMVar_ID_25174 Human_SNP_ID_93227495 A-to-I Human chr2 + 135698224 135698224 135698224 CTCTGTCACCCAGGCTGGAGTGCAGTGGTGCGATGTCGGCTCAGTACAAGCTCCGCCTCCCGGGT CTCTGTCACCCAGGCTGGAGTGCAGTGGTGCGCTGTCGGCTCAGTACAAGCTCCGCCTCCCGGGT A C R3HDM1 Ensembl:ENSG00000048991 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1044048661 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_203406,RMVar_hsa_circ_97196,RMVar_hsa_circ_375158,RMVar_hsa_circ_203426,RMVar_hsa_circ_81201,RMVar_hsa_circ_34570,RMVar_hsa_circ_71999,RMVar_hsa_circ_203430,RMVar_hsa_circ_126534,RMVar_hsa_circ_203442,RMVar_hsa_circ_9114,RMVar_hsa_circ_13702,RMVar_hsa_circ_21133,RMVar_hsa_circ_203452,RMVar_hsa_circ_203455,RMVar_hsa_circ_116607,RMVar_hsa_circ_354616,RMVar_hsa_circ_378696,RMVar_hsa_circ_373970,RMVar_hsa_circ_299194,RMVar_hsa_circ_203457,RMVar_hsa_circ_203456,RMVar_hsa_circ_203453,RMVar_hsa_circ_203454,RMVar_hsa_circ_333893,RMVar_hsa_circ_112476,RMVar_hsa_circ_203461,RMVar_hsa_circ_203462 25175 RMVar_ID_25175 Human_SNP_ID_93232385 A-to-I Human chr2 + 135718514 135718514 135718514 GTTTGTTGTTGTTTGTTTTGAGACACTGTCTTATTCCATCGCCCAGGCTGCAGTGCAGTGGTGCA GTTTGTTGTTGTTTGTTTTGAGACACTGTCTTGTTCCATCGCCCAGGCTGCAGTGCAGTGGTGCA A G R3HDM1 Ensembl:ENSG00000048991 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924221201 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81201,RMVar_hsa_circ_203430,RMVar_hsa_circ_116607,RMVar_hsa_circ_354616,RMVar_hsa_circ_203453,RMVar_hsa_circ_203454,RMVar_hsa_circ_112476,RMVar_hsa_circ_126760,RMVar_hsa_circ_203462,RMVar_hsa_circ_310782,RMVar_hsa_circ_203465 25176 RMVar_ID_25176 Human_SNP_ID_93232396 A-to-I Human chr2 + 135718560 135718560 135718560 GCTGCAGTGCAGTGGTGCACTTGTGGCTCGCTACAGCCTTAACCTCCCCGGGCTCAGATGATCCT GCTGCAGTGCAGTGGTGCACTTGTGGCTCGCTGCAGCCTTAACCTCCCCGGGCTCAGATGATCCT A G R3HDM1 Ensembl:ENSG00000048991 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1481122479 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81201,RMVar_hsa_circ_203430,RMVar_hsa_circ_116607,RMVar_hsa_circ_354616,RMVar_hsa_circ_203453,RMVar_hsa_circ_203454,RMVar_hsa_circ_112476,RMVar_hsa_circ_126760,RMVar_hsa_circ_203462,RMVar_hsa_circ_310782,RMVar_hsa_circ_203465 25177 RMVar_ID_25177 Human_SNP_ID_93232712 A-to-I Human chr2 + 135720029 135720029 135720029 CATACGCCTGGCTAATTTTTTGTGTTTTTAGGAGAGACGGGGTTTCACCATGTTGGCCAGGCTGA CATACGCCTGGCTAATTTTTTGTGTTTTTAGGGGAGACGGGGTTTCACCATGTTGGCCAGGCTGA A G R3HDM1 Ensembl:ENSG00000048991 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs557720609 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81201,RMVar_hsa_circ_203430,RMVar_hsa_circ_116607,RMVar_hsa_circ_354616,RMVar_hsa_circ_203453,RMVar_hsa_circ_203454,RMVar_hsa_circ_112476,RMVar_hsa_circ_126760,RMVar_hsa_circ_203462,RMVar_hsa_circ_310782,RMVar_hsa_circ_203465 25178 RMVar_ID_25178 Human_SNP_ID_93232956 A-to-I Human chr2 + 135721363 135721363 135721363 AGGCATGGTAGTTTGTGCTTGTAGTCCCAGCTACTTGTGAGGCTGAGGCAGGAAGATCACTTGAA AGGCATGGTAGTTTGTGCTTGTAGTCCCAGCTGCTTGTGAGGCTGAGGCAGGAAGATCACTTGAA A G R3HDM1 Ensembl:ENSG00000048991 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1033434974 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81201,RMVar_hsa_circ_203430,RMVar_hsa_circ_116607,RMVar_hsa_circ_354616,RMVar_hsa_circ_203453,RMVar_hsa_circ_203454,RMVar_hsa_circ_112476,RMVar_hsa_circ_126760,RMVar_hsa_circ_203462,RMVar_hsa_circ_310782,RMVar_hsa_circ_203465 25179 RMVar_ID_25179 Human_SNP_ID_93233405 A-to-I Human chr2 + 135723565 135723565 135723565 AGGCTGAGGCAGGTGGATTGCCTGAACTCAGGAGTTCGAGACCAGCCTGGCCAATATGGTGAAAC AGGCTGAGGCAGGTGGATTGCCTGAACTCAGGGGTTCGAGACCAGCCTGGCCAATATGGTGAAAC A G R3HDM1 Ensembl:ENSG00000048991 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs990264680 Functional Loss SNV dbSNP153 33..33 33 - - - 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 25180 RMVar_ID_25180 Human_SNP_ID_93242502 A-to-I Human chr2 + 135760167 135760167 135760167 GTCACCCATAAAGTTACACATGGGCCAGGTACAATGGCTCATGCCTGTGATCCCAGTACTTTAGG GTCACCCATAAAGTTACACATGGGCCAGGTACGATGGCTCATGCCTGTGATCCCAGTACTTTAGG A G UBXN4 Ensembl:ENSG00000144224 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1361231804 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569332 RMVar_hsa_circ_286792,RMVar_hsa_circ_324148,RMVar_hsa_circ_358399,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_203471,RMVar_hsa_circ_41961,RMVar_hsa_circ_60143,RMVar_hsa_circ_358321,RMVar_hsa_circ_274740,RMVar_hsa_circ_302406,RMVar_hsa_circ_371040,RMVar_hsa_circ_63064,RMVar_hsa_circ_203477,RMVar_hsa_circ_203478 25181 RMVar_ID_25181 Human_SNP_ID_93242509 A-to-I Human chr2 + 135760197 135760197 135760197 ACAATGGCTCATGCCTGTGATCCCAGTACTTTAGGAGGCCAAGATCAGTTGAGCTCAGGAGTTCG ACAATGGCTCATGCCTGTGATCCCAGTACTTTGGGAGGCCAAGATCAGTTGAGCTCAGGAGTTCG A G UBXN4 Ensembl:ENSG00000144224 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1048328864 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569332 RMVar_hsa_circ_286792,RMVar_hsa_circ_324148,RMVar_hsa_circ_358399,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_203471,RMVar_hsa_circ_41961,RMVar_hsa_circ_60143,RMVar_hsa_circ_358321,RMVar_hsa_circ_274740,RMVar_hsa_circ_302406,RMVar_hsa_circ_371040,RMVar_hsa_circ_63064,RMVar_hsa_circ_203477,RMVar_hsa_circ_203478 25182 RMVar_ID_25182 Human_SNP_ID_93242532 A-to-I Human chr2 + 135760340 135760340 135760340 GTGGCCCCAGCTACTAGGGAGGGTGAAGTAGGAAGATGGCTTGATCCCAGGAGGCGGAGGTTGCA GTGGCCCCAGCTACTAGGGAGGGTGAAGTAGGGAGATGGCTTGATCCCAGGAGGCGGAGGTTGCA A G UBXN4 Ensembl:ENSG00000144224 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs957967420 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569936 RMVar_hsa_circ_286792,RMVar_hsa_circ_324148,RMVar_hsa_circ_358399,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_203471,RMVar_hsa_circ_41961,RMVar_hsa_circ_60143,RMVar_hsa_circ_358321,RMVar_hsa_circ_274740,RMVar_hsa_circ_302406,RMVar_hsa_circ_371040,RMVar_hsa_circ_63064,RMVar_hsa_circ_203477,RMVar_hsa_circ_203478 25183 RMVar_ID_25183 Human_SNP_ID_93245133 A-to-I Human chr2 + 135771306 135771306 135771306 CAAGACTTGCCTGGCCGACATGGTGAAACGCCATCTCTACTAAAAATACAAAAATTAATCGGGTG CAAGACTTGCCTGGCCGACATGGTGAAACGCCGTCTCTACTAAAAATACAAAAATTAATCGGGTG A G UBXN4 Ensembl:ENSG00000144224 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1040886981 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_324148,RMVar_hsa_circ_102610,RMVar_hsa_circ_277775,RMVar_hsa_circ_284026,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_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_327250,RMVar_hsa_circ_55999,RMVar_hsa_circ_120252,RMVar_hsa_circ_203479,RMVar_hsa_circ_109501,RMVar_hsa_circ_203480,RMVar_hsa_circ_203481,RMVar_hsa_circ_203482 25184 RMVar_ID_25184 Human_SNP_ID_93245148 A-to-I Human chr2 + 135771365 135771365 135771365 CGGGTGTGGTGGTGGGCGCCTATAATCCTGCTACTTGGGAGGCTGAGGCAGGAGAATCACTTGAA CGGGTGTGGTGGTGGGCGCCTATAATCCTGCTGCTTGGGAGGCTGAGGCAGGAGAATCACTTGAA A G UBXN4 Ensembl:ENSG00000144224 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1233685024 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_324148,RMVar_hsa_circ_102610,RMVar_hsa_circ_277775,RMVar_hsa_circ_284026,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_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_327250,RMVar_hsa_circ_55999,RMVar_hsa_circ_120252,RMVar_hsa_circ_203479,RMVar_hsa_circ_109501,RMVar_hsa_circ_203480,RMVar_hsa_circ_203481,RMVar_hsa_circ_203482 25185 RMVar_ID_25185 Human_SNP_ID_93245208 A-to-I Human chr2 + 135771626 135771626 135771626 GTCTTGTTGCTCAGGCTAGAGTGCAGTGGCGCAATCTTGGCTCACTGCAACTTCCACCTCCCGAG GTCTTGTTGCTCAGGCTAGAGTGCAGTGGCGCGATCTTGGCTCACTGCAACTTCCACCTCCCGAG A G UBXN4 Ensembl:ENSG00000144224 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs532767423 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_324148,RMVar_hsa_circ_102610,RMVar_hsa_circ_277775,RMVar_hsa_circ_284026,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_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_327250,RMVar_hsa_circ_55999,RMVar_hsa_circ_120252,RMVar_hsa_circ_203479,RMVar_hsa_circ_109501,RMVar_hsa_circ_203480,RMVar_hsa_circ_203481,RMVar_hsa_circ_203482 25186 RMVar_ID_25186 Human_SNP_ID_93245229 A-to-I Human chr2 + 135771692 135771692 135771692 TCAAGCAATTCTCCTGTCCCAGGCTGCCAAGTAGCTGAGGTTACAGGTGCATGCCAACATGCCCA TCAAGCAATTCTCCTGTCCCAGGCTGCCAAGTGGCTGAGGTTACAGGTGCATGCCAACATGCCCA A G UBXN4 Ensembl:ENSG00000144224 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs888728947 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_324148,RMVar_hsa_circ_102610,RMVar_hsa_circ_277775,RMVar_hsa_circ_284026,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_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_327250,RMVar_hsa_circ_55999,RMVar_hsa_circ_120252,RMVar_hsa_circ_203479,RMVar_hsa_circ_109501,RMVar_hsa_circ_203480,RMVar_hsa_circ_203481,RMVar_hsa_circ_203482 25187 RMVar_ID_25187 Human_SNP_ID_93246494 A-to-I Human chr2 + 135776795 135776795 135776795 TTTTGTACTTTTTGTAGAGACAGGGTTTCACCATGTAGCCGGGCTGGTCTTGAACTCCTGGGCTC TTTTGTACTTTTTGTAGAGACAGGGTTTCACCGTGTAGCCGGGCTGGTCTTGAACTCCTGGGCTC A G UBXN4 Ensembl:ENSG00000144224 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903006068 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13622767 RMVar_hsa_circ_324148,RMVar_hsa_circ_102610,RMVar_hsa_circ_203476,RMVar_hsa_circ_65909,RMVar_hsa_circ_203475,RMVar_hsa_circ_371040,RMVar_hsa_circ_107595,RMVar_hsa_circ_68750,RMVar_hsa_circ_203477,RMVar_hsa_circ_327250,RMVar_hsa_circ_55999,RMVar_hsa_circ_203482,RMVar_hsa_circ_290669,RMVar_hsa_circ_203484 25188 RMVar_ID_25188 Human_SNP_ID_93248105 A-to-I Human chr2 + 135783171 135783171 135783171 CCTGCCTCCATCAGCTTCTTATTTAGTATTTCATATGCCCATTAGCCCTATGCTTCAGATGACAC CCTGCCTCCATCAGCTTCTTATTTAGTATTTCGTATGCCCATTAGCCCTATGCTTCAGATGACAC A G UBXN4 Ensembl:ENSG00000144224 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1223116639 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_59417,Human_RBP_ID_6827404,Human_RBP_ID_13622880,Human_RBP_ID_17277933,Human_RBP_ID_17509755,Human_RBP_ID_24486126,Human_RBP_ID_27686963 RMVar_hsa_circ_102610,RMVar_hsa_circ_203476 25189 RMVar_ID_25189 Human_SNP_ID_93281766 A-to-I Human chr2 - 135921170 135921170 135921170 AGTGATGTGAAAGATGAGTCGAACTAGAGTCAAAAAGACTGGACAGGAGGAAAAGGCACTGAGGA AGTGATGTGAAAGATGAGTCGAACTAGAGTCAGAAAGACTGGACAGGAGGAAAAGGCACTGAGGA T C DARS1 Ensembl:ENSG00000115866 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1378061585 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7414,RMVar_hsa_circ_82692,RMVar_hsa_circ_203498,RMVar_hsa_circ_37795,RMVar_hsa_circ_203500,RMVar_hsa_circ_79854,RMVar_hsa_circ_203499,RMVar_hsa_circ_25133,RMVar_hsa_circ_83597,RMVar_hsa_circ_203501,RMVar_hsa_circ_266292,RMVar_hsa_circ_203502,RMVar_hsa_circ_267619,RMVar_hsa_circ_18735,RMVar_hsa_circ_51444,RMVar_hsa_circ_328178,RMVar_hsa_circ_29235,RMVar_hsa_circ_53908,RMVar_hsa_circ_203503 25190 RMVar_ID_25190 Human_SNP_ID_93281773 A-to-I Human chr2 - 135921205 135921205 135921205 TAAGTTTCTGAGCAAGGATGTATTATAGGAATATTAGTGATGTGAAAGATGAGTCGAACTAGAGT TAAGTTTCTGAGCAAGGATGTATTATAGGAATGTTAGTGATGTGAAAGATGAGTCGAACTAGAGT T C DARS1 Ensembl:ENSG00000115866 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1316486964 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7414,RMVar_hsa_circ_82692,RMVar_hsa_circ_203498,RMVar_hsa_circ_37795,RMVar_hsa_circ_203500,RMVar_hsa_circ_79854,RMVar_hsa_circ_203499,RMVar_hsa_circ_25133,RMVar_hsa_circ_83597,RMVar_hsa_circ_203501,RMVar_hsa_circ_266292,RMVar_hsa_circ_203502,RMVar_hsa_circ_267619,RMVar_hsa_circ_18735,RMVar_hsa_circ_51444,RMVar_hsa_circ_328178,RMVar_hsa_circ_29235,RMVar_hsa_circ_53908,RMVar_hsa_circ_203503 25191 RMVar_ID_25191 Human_SNP_ID_93300689 A-to-I Human chr2 + 136003094 136003094 136003094 TTAAAAAAAATTTTTTTTTGAGACAGAGCCTCACTCTGTTGCCCAGGCTGGAGTGCGATGGCACC TTAAAAAAAATTTTTTTTTGAGACAGAGCCTCGCTCTGTTGCCCAGGCTGGAGTGCGATGGCACC A G DARS-AS1 Ensembl:ENSG00000231890 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917137833 Functional Loss SNV dbSNP153 33..33 33 - - - 25192 RMVar_ID_25192 Human_SNP_ID_93851721 A-to-I Human chr2 + 138278940 138278940 138278940 GAGGAGCAAGCTGGACACCACTGTGGGGCTCTAAGAGTCCTGAATTCGTACTGGGTTGGTGAAGA GAGGAGCAAGCTGGACACCACTGTGGGGCTCTGAGAGTCCTGAATTCGTACTGGGTTGGTGAAGA A G RPL15P5 Ensembl:ENSG00000233045 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1465992551 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1885152 25193 RMVar_ID_25193 Human_SNP_ID_93853814 A-to-I Human chr2 + 138288057 138288057 138288057 CTCCCTGATTTTTGTCTTCCACGTCCTGCAGCACTTCTTTATTCTGCTCTTCACCATCACCCTGC CTCCCTGATTTTTGTCTTCCACGTCCTGCAGCGCTTCTTTATTCTGCTCTTCACCATCACCCTGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879017332 Functional Loss SNV dbSNP153 33..33 33 - - - 25194 RMVar_ID_25194 Human_SNP_ID_93853820 A-to-I Human chr2 + 138288080 138288080 138288080 TCCTGCAGCACTTCTTTATTCTGCTCTTCACCATCACCCTGCATATCTGAAGTCCATAGTGTCAG TCCTGCAGCACTTCTTTATTCTGCTCTTCACCGTCACCCTGCATATCTGAAGTCCATAGTGTCAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878969706 Functional Loss SNV dbSNP153 33..33 33 - - - 25195 RMVar_ID_25195 Human_SNP_ID_93853825 A-to-I Human chr2 + 138288092 138288092 138288092 TCTTTATTCTGCTCTTCACCATCACCCTGCATATCTGAAGTCCATAGTGTCAGATTATCACGTAA TCTTTATTCTGCTCTTCACCATCACCCTGCATGTCTGAAGTCCATAGTGTCAGATTATCACGTAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878981250 Functional Loss SNV dbSNP153 33..33 33 - - - 25196 RMVar_ID_25196 Human_SNP_ID_93926141 A-to-I Human chr2 + 138595049 138595049 138595049 TCGCCCAGGCTGGAGTGCAGTGGCGTGATCTCAGCTCACTGCAACCTCTGCTGCCCGGAGTCAAG TCGCCCAGGCTGGAGTGCAGTGGCGTGATCTCTGCTCACTGCAACCTCTGCTGCCCGGAGTCAAG A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs532089645 Functional Loss SNV dbSNP153 33..33 33 - - - 25197 RMVar_ID_25197 Human_SNP_ID_94562349 A-to-I Human chr2 - 141111986 141111986 141111986 GCTGGAGTGCAGTGGCTCGTTCTTGTCTCACTACAAGCTCTGCCTCCCGAGTTCACGCCATTCTC GCTGGAGTGCAGTGGCTCGTTCTTGTCTCACTGCAAGCTCTGCCTCCCGAGTTCACGCCATTCTC T C LRP1B Ensembl:ENSG00000168702 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1055462090 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7347,RMVar_hsa_circ_83201,RMVar_hsa_circ_203551,RMVar_hsa_circ_121478,RMVar_hsa_circ_203553,RMVar_hsa_circ_118491,RMVar_hsa_circ_203571,RMVar_hsa_circ_46118,RMVar_hsa_circ_27103,RMVar_hsa_circ_105959,RMVar_hsa_circ_82511,RMVar_hsa_circ_203601,RMVar_hsa_circ_203606,RMVar_hsa_circ_18654,RMVar_hsa_circ_277903,RMVar_hsa_circ_337854,RMVar_hsa_circ_77134,RMVar_hsa_circ_303590,RMVar_hsa_circ_68307,RMVar_hsa_circ_44305,RMVar_hsa_circ_203611,RMVar_hsa_circ_203616,RMVar_hsa_circ_81775,RMVar_hsa_circ_82773,RMVar_hsa_circ_203619 25198 RMVar_ID_25198 Human_SNP_ID_94626418 A-to-I Human chr2 - 141348783 141348783 141348783 CCAGGTCCCTCCCACAGCACTTGGGAATTCAAAATGACATTTGGCTGGGGACACAACCAAACCAT CCAGGTCCCTCCCACAGCACTTGGGAATTCAATATGACATTTGGCTGGGGACACAACCAAACCAT T A LRP1B Ensembl:ENSG00000168702 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs534531541 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121478,RMVar_hsa_circ_203553,RMVar_hsa_circ_118491,RMVar_hsa_circ_203571,RMVar_hsa_circ_27103,RMVar_hsa_circ_105959,RMVar_hsa_circ_82511,RMVar_hsa_circ_203601,RMVar_hsa_circ_203606,RMVar_hsa_circ_18654,RMVar_hsa_circ_77134,RMVar_hsa_circ_44305,RMVar_hsa_circ_203611,RMVar_hsa_circ_203616,RMVar_hsa_circ_81775,RMVar_hsa_circ_22154,RMVar_hsa_circ_82773,RMVar_hsa_circ_2020,RMVar_hsa_circ_203619 25199 RMVar_ID_25199 Human_SNP_ID_94628271 A-to-I Human chr2 - 141356421 141356421 141356421 TTGACTGTCCATATTTTGAACACTTTTCCTCTATTCAGAAATTACCTGAGTTATCATATTATTGG TTGACTGTCCATATTTTGAACACTTTTCCTCTCTTCAGAAATTACCTGAGTTATCATATTATTGG T G LRP1B Ensembl:ENSG00000168702 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs961529430 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121478,RMVar_hsa_circ_203553,RMVar_hsa_circ_118491,RMVar_hsa_circ_203571,RMVar_hsa_circ_27103,RMVar_hsa_circ_105959,RMVar_hsa_circ_82511,RMVar_hsa_circ_203601,RMVar_hsa_circ_203606,RMVar_hsa_circ_18654,RMVar_hsa_circ_77134,RMVar_hsa_circ_44305,RMVar_hsa_circ_203611,RMVar_hsa_circ_203616,RMVar_hsa_circ_81775,RMVar_hsa_circ_22154,RMVar_hsa_circ_82773,RMVar_hsa_circ_2020,RMVar_hsa_circ_203619 25200 RMVar_ID_25200 Human_SNP_ID_94693153 A-to-I Human chr2 - 141607740 141607740 141607740 TTTTTTATTTTTAGTACGGATGAGGTCTCACTATGTTGTCCAGGCTGATCTCGAACTCCTGAACT TTTTTTATTTTTAGTACGGATGAGGTCTCACTGTGTTGTCCAGGCTGATCTCGAACTCCTGAACT T C LRP1B Ensembl:ENSG00000168702 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1479065610 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9941640,Human_RBP_ID_13625384,Human_RBP_ID_25580933 RMVar_hsa_circ_121478,RMVar_hsa_circ_203553,RMVar_hsa_circ_118491,RMVar_hsa_circ_203571,RMVar_hsa_circ_82511,RMVar_hsa_circ_203606,RMVar_hsa_circ_18654,RMVar_hsa_circ_77134,RMVar_hsa_circ_203611,RMVar_hsa_circ_203616,RMVar_hsa_circ_81775,RMVar_hsa_circ_377585,RMVar_hsa_circ_203629 25201 RMVar_ID_25201 Human_SNP_ID_94714535 A-to-I Human chr2 - 141691797 141691797 141691797 GGATTGTGGAGTGCAGAAGACGTTTAGGTTGAAGATGGAGTTTGGGGAGGAAATAGAAGCCATAT GGATTGTGGAGTGCAGAAGACGTTTAGGTTGACGATGGAGTTTGGGGAGGAAATAGAAGCCATAT T G LRP1B Ensembl:ENSG00000168702 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1406248686 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22982261 RMVar_hsa_circ_121478,RMVar_hsa_circ_203553,RMVar_hsa_circ_118491,RMVar_hsa_circ_203571,RMVar_hsa_circ_82511,RMVar_hsa_circ_203606,RMVar_hsa_circ_18654,RMVar_hsa_circ_77134,RMVar_hsa_circ_203611,RMVar_hsa_circ_203616,RMVar_hsa_circ_81775,RMVar_hsa_circ_377585,RMVar_hsa_circ_203629 25202 RMVar_ID_25202 Human_SNP_ID_94723734 A-to-I Human chr2 - 141729147 141729147 141729147 AAAACAGGTTCCAGCTGAGGCAGTCTTAACACAGCTCCTAATGGCCAGGCTCCCTTTGGCTCACC AAAACAGGTTCCAGCTGAGGCAGTCTTAACACGGCTCCTAATGGCCAGGCTCCCTTTGGCTCACC T C LRP1B Ensembl:ENSG00000168702 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs570560221 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121478,RMVar_hsa_circ_203553,RMVar_hsa_circ_118491,RMVar_hsa_circ_203571,RMVar_hsa_circ_82511,RMVar_hsa_circ_203606,RMVar_hsa_circ_18654,RMVar_hsa_circ_77134,RMVar_hsa_circ_203611,RMVar_hsa_circ_203616,RMVar_hsa_circ_81775,RMVar_hsa_circ_377585,RMVar_hsa_circ_203629 25203 RMVar_ID_25203 Human_SNP_ID_94723750 A-to-I Human chr2 - 141729223 141729223 141729223 TGGCTGATGCCCCCAAGGAAGTCCTGTGGTAAAGCTGTCAGGGGAAGCTGTAGGTAAGCACTTGA TGGCTGATGCCCCCAAGGAAGTCCTGTGGTAAGGCTGTCAGGGGAAGCTGTAGGTAAGCACTTGA T C LRP1B Ensembl:ENSG00000168702 Protein coding intron GSE107867 ASD brains,cerebellum;ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1190806674 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121478,RMVar_hsa_circ_203553,RMVar_hsa_circ_118491,RMVar_hsa_circ_203571,RMVar_hsa_circ_82511,RMVar_hsa_circ_203606,RMVar_hsa_circ_18654,RMVar_hsa_circ_77134,RMVar_hsa_circ_203611,RMVar_hsa_circ_203616,RMVar_hsa_circ_81775,RMVar_hsa_circ_377585,RMVar_hsa_circ_203629 25204 RMVar_ID_25204 Human_SNP_ID_94727505 A-to-I Human chr2 - 141743686 141743686 141743686 CATGAGAAACTCCAAAACCAGAACATTTTATTACGGCTTTAGTGTTGTTGCTTGCTATTGAACAG CATGAGAAACTCCAAAACCAGAACATTTTATTGCGGCTTTAGTGTTGTTGCTTGCTATTGAACAG T C LRP1B Ensembl:ENSG00000168702 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1196702537 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121478,RMVar_hsa_circ_203553,RMVar_hsa_circ_118491,RMVar_hsa_circ_203571,RMVar_hsa_circ_82511,RMVar_hsa_circ_203606,RMVar_hsa_circ_18654,RMVar_hsa_circ_77134,RMVar_hsa_circ_203611,RMVar_hsa_circ_203616,RMVar_hsa_circ_81775,RMVar_hsa_circ_377585,RMVar_hsa_circ_203629 25205 RMVar_ID_25205 Human_SNP_ID_94727506 A-to-I Human chr2 - 141743689 141743689 141743689 AGCCATGAGAAACTCCAAAACCAGAACATTTTATTACGGCTTTAGTGTTGTTGCTTGCTATTGAA AGCCATGAGAAACTCCAAAACCAGAACATTTTCTTACGGCTTTAGTGTTGTTGCTTGCTATTGAA T G LRP1B Ensembl:ENSG00000168702 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1325376609 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121478,RMVar_hsa_circ_203553,RMVar_hsa_circ_118491,RMVar_hsa_circ_203571,RMVar_hsa_circ_82511,RMVar_hsa_circ_203606,RMVar_hsa_circ_18654,RMVar_hsa_circ_77134,RMVar_hsa_circ_203611,RMVar_hsa_circ_203616,RMVar_hsa_circ_81775,RMVar_hsa_circ_377585,RMVar_hsa_circ_203629 25206 RMVar_ID_25206 Human_SNP_ID_94762147 A-to-I Human chr2 - 141882848 141882848 141882848 ACCTCAAGATAAAAAAAACAGAATGTGTGCCTATAACCCCTGCACTTTGAGAGGCTGAGGTGGTA ACCTCAAGATAAAAAAAACAGAATGTGTGCCTGTAACCCCTGCACTTTGAGAGGCTGAGGTGGTA T C LRP1B Ensembl:ENSG00000168702 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs921598903 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77134,RMVar_hsa_circ_203611 25207 RMVar_ID_25207 Human_SNP_ID_94784479 A-to-I Human chr2 - 141970169 141970169 141970169 AAGCCAGATGTCTGATAAATGGTTAATATGCAAAATATGTAAGGATCTCAAACAACACTATAGAA AAGCCAGATGTCTGATAAATGGTTAATATGCACAATATGTAAGGATCTCAAACAACACTATAGAA T G LRP1B Ensembl:ENSG00000168702 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1159873249 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77134,RMVar_hsa_circ_203611,RMVar_hsa_circ_203637 25208 RMVar_ID_25208 Human_SNP_ID_94803280 A-to-I Human chr2 - 142044264 142044264 142044264 TAATCAGTGATTCAGAATTAGAAATTCCAAGTAGAAATTCACCCACGGATAGAAGAATCTAATTC TAATCAGTGATTCAGAATTAGAAATTCCAAGTGGAAATTCACCCACGGATAGAAGAATCTAATTC T C LRP1B Ensembl:ENSG00000168702 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,temporal_cortex - 29129909,30559470 RNA-Seq:(High) rs1387783610 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13628028 RMVar_hsa_circ_77134,RMVar_hsa_circ_203611 25209 RMVar_ID_25209 Human_SNP_ID_94821658 A-to-I Human chr2 - 142116105 142116105 142116105 CACTCCAACCTCCTCCTCCCAGGCTCTTGAGTAGCTGGGACTACAGGCATATGCAACCGCACCCA CACTCCAACCTCCTCCTCCCAGGCTCTTGAGTGGCTGGGACTACAGGCATATGCAACCGCACCCA T C LRP1B Ensembl:ENSG00000168702 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1451523605 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13629339 RMVar_hsa_circ_77134,RMVar_hsa_circ_203611 25210 RMVar_ID_25210 Human_SNP_ID_95043283 A-to-I Human chr2 + 143013019 143013019 143013019 TCTTATTAATTTTTTAGAGACAAAGTCTCACTATGTTGTCCAGGCTGGAGTGTGATGGCTATTCA TCTTATTAATTTTTTAGAGACAAAGTCTCACTGTGTTGTCCAGGCTGGAGTGTGATGGCTATTCA A G KYNU Ensembl:ENSG00000115919 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs967948875 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13629772 RMVar_hsa_circ_203643,RMVar_hsa_circ_84672 25211 RMVar_ID_25211 Human_SNP_ID_95046780 A-to-I Human chr2 + 143028383 143028383 143028383 TCTCCTGCCTCAGCCTCCTGGTAGCTGGGACTACAGGTGTATGCCACCACGCCCGTCTAATTTTT TCTCCTGCCTCAGCCTCCTGGTAGCTGGGACTGCAGGTGTATGCCACCACGCCCGTCTAATTTTT A G KYNU Ensembl:ENSG00000115919 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1441661792 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_203643,RMVar_hsa_circ_84672 25212 RMVar_ID_25212 Human_SNP_ID_95047264 A-to-I Human chr2 + 143030529 143030522 143030529 ACAAGGTCTTGTTCTGTCACCTAGGCCGGAGTACAGTGGTGCGATCAGGCTCAGTTCAGCCTTGA ACAAGGTCTTGTTCTGTCACCTAGGC_______CAGTGGTGCGATCAGGCTCAGTTCAGCCTTGA CCGGAGTA C KYNU Ensembl:ENSG00000115919 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1485170244 Functional Loss DEL dbSNP153 27..33 33 - - - RMVar_hsa_circ_60123,RMVar_hsa_circ_203643,RMVar_hsa_circ_84672,RMVar_hsa_circ_337541,RMVar_hsa_circ_203644 25213 RMVar_ID_25213 Human_SNP_ID_95049642 A-to-I Human chr2 + 143040503 143040503 143040503 TTTTGCTAACTGGCTATCTGGAATACCTGATCAAGCATAACTATGGCAAAGATAAAGCAGCAACC TTTTGCTAACTGGCTATCTGGAATACCTGATCGAGCATAACTATGGCAAAGATAAAGCAGCAACC A G KYNU Ensembl:ENSG00000115919 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1182196513 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_301326,Human_Splice_Rec_301352 RMVar_hsa_circ_60123 25214 RMVar_ID_25214 Human_SNP_ID_95051879 A-to-I Human chr2 + 143048832 143048831 143048832 GCCATCTCATGCCAGTCAGAATGGCAATCATTAAAAAGTCAGGAAACAATAGATGCTGGTGAGGC GCCATCTCATGCCAGTCAGAATGGCAATCATT_AAAAGTCAGGAAACAATAGATGCTGGTGAGGC TA T KYNU Ensembl:ENSG00000115919 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1218627118 Functional Loss DEL dbSNP153 33..33 33 - - - 25215 RMVar_ID_25215 Human_SNP_ID_95273843 A-to-I Human chr2 - 143946911 143946909 143946911 CTGAGCCTGGCTGCTTGTCATAGCTGACACAGAGCCATCTGCCACAAACCTGTGGCGGCTTCAGA CTGAGCCTGGCTGCTTGTCATAGCTGACACAG__CCATCTGCCACAAACCTGTGGCGGCTTCAGA GCT G GTDC1 Ensembl:ENSG00000121964 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215244564 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_203656,RMVar_hsa_circ_203660,RMVar_hsa_circ_203658,RMVar_hsa_circ_203657,RMVar_hsa_circ_203659 25216 RMVar_ID_25216 Human_SNP_ID_96216156 A-to-I Human chr2 + 147848594 147848594 147848594 AAGAAAACCAAATACCACATGTTCCTATAAGTAGGAGCAAAATGATGAGAAAACATGAAAACAAA AAGAAAACCAAATACCACATGTTCCTATAAGTGGGAGCAAAATGATGAGAAAACATGAAAACAAA A G ACVR2A Ensembl:ENSG00000121989 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,cerebellum - 29129909,30559470 RNA-Seq:(High) rs1413006327 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9565,RMVar_hsa_circ_265735,RMVar_hsa_circ_39406,RMVar_hsa_circ_369491,RMVar_hsa_circ_203697 25217 RMVar_ID_25217 Human_SNP_ID_96257481 A-to-I Human chr2 - 148021497 148021465 148021498 GGCCAAGCAGCAGCAGTAGCAGCAGCAGCAGTAGCAGCAGCAGCAGCAACAGCAGCAGCAGCAGC GGCCAAGCAGCAGCAGTAGCAGCAGCAGCAG_________________________________C GCTGCTGCTGCTGCTGTTGCTGCTGCTGCTGCTA G ORC4 Ensembl:ENSG00000115947 Protein coding 5'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1186749233 Functional Loss DEL dbSNP153 32..64 33 - - - Human_Splice_Rec_304261,Human_Splice_Rec_304331 RMVar_hsa_circ_88979,RMVar_hsa_circ_203718 25218 RMVar_ID_25218 Human_SNP_ID_96257486 A-to-I Human chr2 - 148021497 148021471 148021498 GGCCAAGCAGCAGCAGTAGCAGCAGCAGCAGTAGCAGCAGCAGCAGCAACAGCAGCAGCAGCAGC GGCCAAGCAGCAGCAGTAGCAGCAGCAGCAG___________________________CAGCAGC GCTGCTGCTGTTGCTGCTGCTGCTGCTA G ORC4 Ensembl:ENSG00000115947 Protein coding 5'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1373757641 Functional Loss DEL dbSNP153 32..58 33 - - - Human_Splice_Rec_304261,Human_Splice_Rec_304331 RMVar_hsa_circ_88979,RMVar_hsa_circ_203718 25219 RMVar_ID_25219 Human_SNP_ID_96257493 A-to-I Human chr2 - 148021497 148021477 148021498 GGCCAAGCAGCAGCAGTAGCAGCAGCAGCAGTAGCAGCAGCAGCAGCAACAGCAGCAGCAGCAGC GGCCAAGCAGCAGCAGTAGCAGCAGCAGCAG_____________________CAGCAGCAGCAGC GCTGTTGCTGCTGCTGCTGCTA G ORC4 Ensembl:ENSG00000115947 Protein coding 5'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1160900172 Functional Loss DEL dbSNP153 32..52 33 - - - Human_Splice_Rec_304261,Human_Splice_Rec_304331 RMVar_hsa_circ_88979,RMVar_hsa_circ_203718 25220 RMVar_ID_25220 Human_SNP_ID_96257514 A-to-I Human chr2 - 148021497 148021483 148021498 GGCCAAGCAGCAGCAGTAGCAGCAGCAGCAGTAGCAGCAGCAGCAGCAACAGCAGCAGCAGCAGC GGCCAAGCAGCAGCAGTAGCAGCAGCAGCAG_______________CAACAGCAGCAGCAGCAGC GCTGCTGCTGCTGCTA G ORC4 Ensembl:ENSG00000115947 Protein coding 5'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs755361381 Functional Loss DEL dbSNP153 32..46 33 - - - Human_Splice_Rec_304261,Human_Splice_Rec_304331 RMVar_hsa_circ_88979,RMVar_hsa_circ_203718 25221 RMVar_ID_25221 Human_SNP_ID_96257516 A-to-I Human chr2 - 148021512 148021486 148021513 GATGTCTCCAGCCAGGGCCAAGCAGCAGCAGTAGCAGCAGCAGCAGTAGCAGCAGCAGCAGCAAC GATGTCTCCAGCCAGGGCCAAGCAGCAGCAG___________________________CAGCAAC GCTGCTGCTGCTACTGCTGCTGCTGCTA G ORC4 Ensembl:ENSG00000115947 Protein coding 5'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs970689941 Functional Loss DEL dbSNP153 32..58 33 - - - Human_Splice_Rec_304261,Human_Splice_Rec_304331 RMVar_hsa_circ_88979,RMVar_hsa_circ_203718 25222 RMVar_ID_25222 Human_SNP_ID_96257517 A-to-I Human chr2 - 148021497 148021486 148021498 GGCCAAGCAGCAGCAGTAGCAGCAGCAGCAGTAGCAGCAGCAGCAGCAACAGCAGCAGCAGCAGC GGCCAAGCAGCAGCAGTAGCAGCAGCAGCAG____________CAGCAACAGCAGCAGCAGCAGC GCTGCTGCTGCTA G ORC4 Ensembl:ENSG00000115947 Protein coding 5'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1173593818 Functional Loss DEL dbSNP153 32..43 33 - - - Human_Splice_Rec_304261,Human_Splice_Rec_304331 RMVar_hsa_circ_88979,RMVar_hsa_circ_203718 25223 RMVar_ID_25223 Human_SNP_ID_96257523 A-to-I Human chr2 - 148021497 148021492 148021498 GGCCAAGCAGCAGCAGTAGCAGCAGCAGCAGTAGCAGCAGCAGCAGCAACAGCAGCAGCAGCAGC GGCCAAGCAGCAGCAGTAGCAGCAGCAGCAG______CAGCAGCAGCAACAGCAGCAGCAGCAGC GCTGCTA G ORC4 Ensembl:ENSG00000115947 Protein coding 5'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1053396305 Functional Loss DEL dbSNP153 32..37 33 - - - Human_Splice_Rec_304261,Human_Splice_Rec_304331 RMVar_hsa_circ_88979,RMVar_hsa_circ_203718 25224 RMVar_ID_25224 Human_SNP_ID_96257526 A-to-I Human chr2 - 148021497 148021495 148021498 GGCCAAGCAGCAGCAGTAGCAGCAGCAGCAGTAGCAGCAGCAGCAGCAACAGCAGCAGCAGCAGC GGCCAAGCAGCAGCAGTAGCAGCAGCAGCAG___CAGCAGCAGCAGCAACAGCAGCAGCAGCAGC GCTA G ORC4 Ensembl:ENSG00000115947 Protein coding 5'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs889486657 Functional Loss DEL dbSNP153 32..34 33 - - - Human_Splice_Rec_304261,Human_Splice_Rec_304331 RMVar_hsa_circ_88979,RMVar_hsa_circ_203718 25225 RMVar_ID_25225 Human_SNP_ID_96257536 A-to-I Human chr2 - 148021512 148021501 148021513 GATGTCTCCAGCCAGGGCCAAGCAGCAGCAGTAGCAGCAGCAGCAGTAGCAGCAGCAGCAGCAAC GATGTCTCCAGCCAGGGCCAAGCAGCAGCAG____________CAGTAGCAGCAGCAGCAGCAAC GCTGCTGCTGCTA G ORC4 Ensembl:ENSG00000115947 Protein coding 5'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1416304352 Functional Loss DEL dbSNP153 32..43 33 - - - Human_Splice_Rec_304261,Human_Splice_Rec_304331 RMVar_hsa_circ_88979,RMVar_hsa_circ_203718 25226 RMVar_ID_25226 Human_SNP_ID_96261672 A-to-I Human chr2 + 148040223 148040223 148040223 AAAGTAATAACTAAATAAATAACAAATAAGCTAGACATGGTGGCACGAGCCTGTAGTCCCAGAAG AAAGTAATAACTAAATAAATAACAAATAAGCTGGACATGGTGGCACGAGCCTGTAGTCCCAGAAG A G MBD5 Ensembl:ENSG00000204406 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs566363580 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569945 RMVar_hsa_circ_203721,RMVar_hsa_circ_376151,RMVar_hsa_circ_293763 25227 RMVar_ID_25227 Human_SNP_ID_96261888 A-to-I Human chr2 + 148041073 148041073 148041073 TAGCCTCAACCTCCGGGCTTAAGTGATCCTCTAACCTCAGCCTCCTGGGACTAAAGGCTCATGCC TAGCCTCAACCTCCGGGCTTAAGTGATCCTCTCACCTCAGCCTCCTGGGACTAAAGGCTCATGCC A C MBD5 Ensembl:ENSG00000204406 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1479075867 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_203721,RMVar_hsa_circ_376151,RMVar_hsa_circ_293763 25228 RMVar_ID_25228 Human_SNP_ID_96261892 A-to-I Human chr2 + 148041093 148041093 148041093 AAGTGATCCTCTAACCTCAGCCTCCTGGGACTAAAGGCTCATGCCACCATGCCCAGCTTATTTAT AAGTGATCCTCTAACCTCAGCCTCCTGGGACTGAAGGCTCATGCCACCATGCCCAGCTTATTTAT A G MBD5 Ensembl:ENSG00000204406 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs568000410 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_203721,RMVar_hsa_circ_376151,RMVar_hsa_circ_293763 25229 RMVar_ID_25229 Human_SNP_ID_96267818 A-to-I Human chr2 + 148066072 148066072 148066072 CACGGTGGTTTCCACCTGTAATCCCAGCACTTAAGGAGGCAAAGGGAGGAGGATCAAGACAAGCC CACGGTGGTTTCCACCTGTAATCCCAGCACTTCAGGAGGCAAAGGGAGGAGGATCAAGACAAGCC A C MBD5 Ensembl:ENSG00000204406 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs149447747 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_203721,RMVar_hsa_circ_376151,RMVar_hsa_circ_293763,RMVar_hsa_circ_288325 25230 RMVar_ID_25230 Human_SNP_ID_96267853 A-to-I Human chr2 + 148066186 148066186 148066186 AAATGAGCCGAGCATGGTGTTGTGCGCCTGTCATCGCAGCTACTTGGAAGGCTGAGGTGGGAGGA AAATGAGCCGAGCATGGTGTTGTGCGCCTGTCCTCGCAGCTACTTGGAAGGCTGAGGTGGGAGGA A C MBD5 Ensembl:ENSG00000204406 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049947271 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569946,Human_RBP_ID_22598889 RMVar_hsa_circ_203721,RMVar_hsa_circ_376151,RMVar_hsa_circ_293763,RMVar_hsa_circ_288325 25231 RMVar_ID_25231 Human_SNP_ID_96267854 A-to-I Human chr2 + 148066186 148066186 148066186 AAATGAGCCGAGCATGGTGTTGTGCGCCTGTCATCGCAGCTACTTGGAAGGCTGAGGTGGGAGGA AAATGAGCCGAGCATGGTGTTGTGCGCCTGTCTTCGCAGCTACTTGGAAGGCTGAGGTGGGAGGA A T MBD5 Ensembl:ENSG00000204406 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049947271 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569946,Human_RBP_ID_22598889 RMVar_hsa_circ_203721,RMVar_hsa_circ_376151,RMVar_hsa_circ_293763,RMVar_hsa_circ_288325 25232 RMVar_ID_25232 Human_SNP_ID_96267957 A-to-I Human chr2 + 148066556 148066556 148066556 TCACCCAGGCTGGAGTGCAATGGCATAATCTCAGCTCACTGCAACCTCCACCTCCCAGTTTTTCC TCACCCAGGCTGGAGTGCAATGGCATAATCTCGGCTCACTGCAACCTCCACCTCCCAGTTTTTCC A G MBD5 Ensembl:ENSG00000204406 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs897245482 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_203721,RMVar_hsa_circ_376151,RMVar_hsa_circ_293763,RMVar_hsa_circ_288325 25233 RMVar_ID_25233 Human_SNP_ID_96281359 A-to-I Human chr2 + 148127050 148127050 148127050 CCAGGCTGGAGTGCGTGGCGCGATCTCGGCTCACTGCAAGCTCCGCCTCCCGGGTTCGGGCGATT CCAGGCTGGAGTGCGTGGCGCGATCTCGGCTCGCTGCAAGCTCCGCCTCCCGGGTTCGGGCGATT A G MBD5 Ensembl:ENSG00000204406 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1004050341 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_203721,RMVar_hsa_circ_376151,RMVar_hsa_circ_293763,RMVar_hsa_circ_288325 25234 RMVar_ID_25234 Human_SNP_ID_96317368 A-to-I Human chr2 + 148279322 148279322 148279322 TGTGGTGGCATGAGCCTATAGTCCTAGATACTAGGAAGGTCAAGTCGGCAGGATCGTTTAAGCAC TGTGGTGGCATGAGCCTATAGTCCTAGATACTGGGAAGGTCAAGTCGGCAGGATCGTTTAAGCAC A G MBD5 Ensembl:ENSG00000204406 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973573070 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_203725,RMVar_hsa_circ_203721,RMVar_hsa_circ_376151,RMVar_hsa_circ_293763,RMVar_hsa_circ_373535,RMVar_hsa_circ_295945,RMVar_hsa_circ_117348,RMVar_hsa_circ_128170,RMVar_hsa_circ_203726,RMVar_hsa_circ_9723,RMVar_hsa_circ_203724,RMVar_hsa_circ_282371 25235 RMVar_ID_25235 Human_SNP_ID_96405466 A-to-I Human chr2 + 148646999 148646999 148646999 GGGCCTGGTGGTGCGCGCCTGTAATACCAGCTACTCGGGAGGCTGAGGCAGAAGAATTGCTTGAA GGGCCTGGTGGTGCGCGCCTGTAATACCAGCTGCTCGGGAGGCTGAGGCAGAAGAATTGCTTGAA A G EPC2 Ensembl:ENSG00000135999 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1364918921 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_203733,RMVar_hsa_circ_83945,RMVar_hsa_circ_127128,RMVar_hsa_circ_203734 25236 RMVar_ID_25236 Human_SNP_ID_96407420 A-to-I Human chr2 + 148654551 148654551 148654551 GGAGTGGCATGTACCTGTAGTCTCAGCTACTTAGGAGGCTGAAACTGGAGGATTCCTTGAGCCCG GGAGTGGCATGTACCTGTAGTCTCAGCTACTTGGGAGGCTGAAACTGGAGGATTCCTTGAGCCCG A G EPC2 Ensembl:ENSG00000135999 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs961699252 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13634047 RMVar_hsa_circ_203733,RMVar_hsa_circ_83945,RMVar_hsa_circ_127128,RMVar_hsa_circ_203734 25237 RMVar_ID_25237 Human_SNP_ID_96434092 A-to-I Human chr2 + 148760177 148760177 148760177 GAGGAGGGAGGCTGAGGCAGGAGAATCGCTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCTGAGA GAGGAGGGAGGCTGAGGCAGGAGAATCGCTTGCACCTGGGAGGCAGAGGTTGCAGTGAGCTGAGA A C EPC2 Ensembl:ENSG00000135999 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348541683 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108940,RMVar_hsa_circ_203733,RMVar_hsa_circ_83945,RMVar_hsa_circ_127128,RMVar_hsa_circ_203734,RMVar_hsa_circ_203736,RMVar_hsa_circ_375224,RMVar_hsa_circ_71927,RMVar_hsa_circ_40735,RMVar_hsa_circ_349909,RMVar_hsa_circ_299384,RMVar_hsa_circ_203738,RMVar_hsa_circ_203739,RMVar_hsa_circ_64092 25238 RMVar_ID_25238 Human_SNP_ID_96493555 A-to-I Human chr2 + 149015163 149015163 149015163 TGAGCCGAGATTGTGCCACTGCACTCCAGCCTAGGTGACAAAGTGAGAGCCTATCTAAAAAACAT TGAGCCGAGATTGTGCCACTGCACTCCAGCCTGGGTGACAAAGTGAGAGCCTATCTAAAAAACAT A G KIF5C Ensembl:ENSG00000168280 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1018741147 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269500,RMVar_hsa_circ_117946,RMVar_hsa_circ_203767 25239 RMVar_ID_25239 Human_SNP_ID_96494257 A-to-I Human chr2 + 149018600 149018600 149018600 CCTATAATCCCAGCACTTTGGGAGGCCAAGGCAGGAGGATCACTTGAGGCCAGGCGTTTGAAACC CCTATAATCCCAGCACTTTGGGAGGCCAAGGCGGGAGGATCACTTGAGGCCAGGCGTTTGAAACC A G KIF5C Ensembl:ENSG00000168280 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs908153222 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269500,RMVar_hsa_circ_117946,RMVar_hsa_circ_203767 25240 RMVar_ID_25240 Human_SNP_ID_344990752 A-to-I Human chr7 - 150232607 150232607 150232607 GTTGGCTAGGCTGGCCTTGAACTCCTGACCTCAGGTGATCTGCCTGCCTCAGCCTCCCAAAGTGC GTTGGCTAGGCTGGCCTTGAACTCCTGACCTCGGGTGATCTGCCTGCCTCAGCCTCCCAAAGTGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs915419509 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29925,RMVar_hsa_circ_299320,RMVar_hsa_circ_121673,RMVar_hsa_circ_249385 25241 RMVar_ID_25241 Human_SNP_ID_345009939 A-to-I Human chr7 - 150319482 150319482 150319482 TTGTTCTGGGCCAGGCGAGGTGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCCGAGGCAGGC TTGTTCTGGGCCAGGCGAGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGC T C ACTR3C Ensembl:ENSG00000106526 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1472706458 Functional Loss SNV dbSNP153 33..33 33 - - - 25242 RMVar_ID_25242 Human_SNP_ID_345010546 A-to-I Human chr7 - 150322297 150322297 150322297 TTGTGCCAACCTTCTGTCTCATCCTGTGACTTAGAATGCCTAACCTCCTATGAATGCAGCCTCAT TTGTGCCAACCTTCTGTCTCATCCTGTGACTTGGAATGCCTAACCTCCTATGAATGCAGCCTCAT T C ACTR3C Ensembl:ENSG00000106526 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs375054563 Functional Loss SNV dbSNP153 33..33 33 - - - 25243 RMVar_ID_25243 Human_SNP_ID_345017548 A-to-I Human chr7 + 150347853 150347853 150347853 GTGGTAGTCCCAGCTGCTTGGGGGGCTGAGGCAAGAGGATCCCTTGAACCTCAAGGAGGTTGAGG GTGGTAGTCCCAGCTGCTTGGGGGGCTGAGGCGAGAGGATCCCTTGAACCTCAAGGAGGTTGAGG 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 GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031377177 Functional Loss SNV dbSNP153 33..33 33 - - - 25244 RMVar_ID_25244 Human_SNP_ID_345042419 A-to-I Human chr7 + 150442189 150442189 150442189 GCCTTTCTCATTCCATCAAGTATGTGGGTAGCAGGAAGGGGAAACTCTGGGGCCTGAGGGTACCC GCCTTTCTCATTCCATCAAGTATGTGGGTAGCGGGAAGGGGAAACTCTGGGGCCTGAGGGTACCC A G LINC00996 Ensembl:ENSG00000242258 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs12333724 Functional Loss SNV dbSNP153 33..33 33 - - - 25245 RMVar_ID_25245 Human_SNP_ID_345042420 A-to-I Human chr7 + 150442189 150442189 150442189 GCCTTTCTCATTCCATCAAGTATGTGGGTAGCAGGAAGGGGAAACTCTGGGGCCTGAGGGTACCC GCCTTTCTCATTCCATCAAGTATGTGGGTAGCTGGAAGGGGAAACTCTGGGGCCTGAGGGTACCC A T LINC00996 Ensembl:ENSG00000242258 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs12333724 Functional Loss SNV dbSNP153 33..33 33 - - - 25246 RMVar_ID_25246 Human_SNP_ID_345117195 A-to-I Human chr7 + 150721555 150721555 150721555 AGTAAGGGCCGGGCGAGGTGGCTCACGCCTGTAATCCCAACACTTTGGGAGGTCGAGGCAGGTGG AGTAAGGGCCGGGCGAGGTGGCTCACGCCTGTTATCCCAACACTTTGGGAGGTCGAGGCAGGTGG A T GIMAP1,GIMAP1-GIMAP5 Ensembl:ENSG00000213203,Ensembl:ENSG00000281887 Protein coding,Protein coding 3'UTR,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1343273890 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_249403,RMVar_hsa_circ_88155 25247 RMVar_ID_25247 Human_SNP_ID_345124449 A-to-I Human chr7 - 150749954 150749954 150749954 TTGCCCATAGTTTTACCTAGAAATCCAGTTGTAGAATCAAATTGTGAATCCATTACAGCTAATAA TTGCCCATAGTTTTACCTAGAAATCCAGTTGTGGAATCAAATTGTGAATCCATTACAGCTAATAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879214954 Functional Loss SNV dbSNP153 33..33 33 - - - 25248 RMVar_ID_25248 Human_SNP_ID_345199109 A-to-I Human chr7 + 151029606 151029606 151029606 TCGACTGACTGCAACCTCTGCCTCCTGGGTTCAAGCAATTCTCATGCTTCAGCCACCCAAGTAGC TCGACTGACTGCAACCTCTGCCTCCTGGGTTCCAGCAATTCTCATGCTTCAGCCACCCAAGTAGC A C ABCB8 Ensembl:ENSG00000197150 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1300762391 Functional Loss SNV dbSNP153 33..33 33 - - - 25249 RMVar_ID_25249 Human_SNP_ID_345199112 A-to-I Human chr7 + 151029617 151029617 151029617 CAACCTCTGCCTCCTGGGTTCAAGCAATTCTCATGCTTCAGCCACCCAAGTAGCTGGGATTACAG CAACCTCTGCCTCCTGGGTTCAAGCAATTCTCGTGCTTCAGCCACCCAAGTAGCTGGGATTACAG A G ABCB8 Ensembl:ENSG00000197150 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1446361153 Functional Loss SNV dbSNP153 33..33 33 - - - 25250 RMVar_ID_25250 Human_SNP_ID_345199129 A-to-I Human chr7 + 151029706 151029706 151029706 TTGTATTTTTAGTAGAGACGGGGTTTCATCATATTGGTGGGCAGACTGGTCTTCAACTCCTGACC TTGTATTTTTAGTAGAGACGGGGTTTCATCATGTTGGTGGGCAGACTGGTCTTCAACTCCTGACC A G ABCB8 Ensembl:ENSG00000197150 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1265171500 Functional Loss SNV dbSNP153 33..33 33 - - - 25251 RMVar_ID_25251 Human_SNP_ID_345199412 A-to-I Human chr7 + 151030819 151030819 151030819 AAAATTAACCAGGCATGGTGGTGGGCGCCTGTAGTCCCAGCTACTCGAGAGGCTGAGGCAGGAGA AAAATTAACCAGGCATGGTGGTGGGCGCCTGTGGTCCCAGCTACTCGAGAGGCTGAGGCAGGAGA A G ABCB8 Ensembl:ENSG00000197150 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1554443309 Functional Loss SNV dbSNP153 33..33 33 - - - 25252 RMVar_ID_25252 Human_SNP_ID_345199649 A-to-I Human chr7 + 151031650 151031650 151031650 GCCCCTCTGCTATGATCTTTTTTTTTTTTTTCAAGACAGAGTCTTGCTCTGTTGTCCAGGCTGGA GCCCCTCTGCTATGATCTTTTTTTTTTTTTTCTAGACAGAGTCTTGCTCTGTTGTCCAGGCTGGA A T ABCB8 Ensembl:ENSG00000197150 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1445032822 Functional Loss SNV dbSNP153 33..33 33 - - - 25253 RMVar_ID_25253 Human_SNP_ID_345199833 A-to-I Human chr7 + 151032418 151032418 151032418 ACACAGTAGGTTCAAAATGTGTAGAATAGGCCAGGCACGGTGGCTCATACCTGGAATCCCAGCAC ACACAGTAGGTTCAAAATGTGTAGAATAGGCCGGGCACGGTGGCTCATACCTGGAATCCCAGCAC A G ABCB8 Ensembl:ENSG00000197150 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1468182594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16067444 25254 RMVar_ID_25254 Human_SNP_ID_345205186 A-to-I Human chr7 + 151049130 151049130 151049130 CCACCAGACTGCCCTGGATGAGCGAGAAAGCCACCGGCTCATCTTCCCGGCTGTCACCCTGTGCA CCACCAGACTGCCCTGGATGAGCGAGAAAGCCGCCGGCTCATCTTCCCGGCTGTCACCCTGTGCA A G ASIC3 Ensembl:ENSG00000213199 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs759506067 Functional Loss SNV dbSNP153 33..33 33 - - - 25255 RMVar_ID_25255 Human_SNP_ID_345211522 A-to-I Human chr7 + 151068649 151068649 151068649 TCAAGTGATCCTCCTGCCTCAGCCTCCCAAGTAGCTGGAACTACAGGCGCGTGCTACCATGCCTG TCAAGTGATCCTCCTGCCTCAGCCTCCCAAGTTGCTGGAACTACAGGCGCGTGCTACCATGCCTG A T SLC4A2 Ensembl:ENSG00000164889 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1429253427 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91308,RMVar_hsa_circ_100849,RMVar_hsa_circ_249416,RMVar_hsa_circ_108385,RMVar_hsa_circ_249417,RMVar_hsa_circ_249418 25256 RMVar_ID_25256 Human_SNP_ID_345211539 A-to-I Human chr7 + 151068694 151068694 151068694 GGCGCGTGCTACCATGCCTGCCTAATTGTTTTATTTTTAGTAGAGATGGGGTTTCACCATGTTGC GGCGCGTGCTACCATGCCTGCCTAATTGTTTTGTTTTTAGTAGAGATGGGGTTTCACCATGTTGC A G SLC4A2 Ensembl:ENSG00000164889 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs937347901 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91308,RMVar_hsa_circ_100849,RMVar_hsa_circ_249416,RMVar_hsa_circ_108385,RMVar_hsa_circ_249417,RMVar_hsa_circ_249418 25257 RMVar_ID_25257 Human_SNP_ID_345211595 A-to-I Human chr7 + 151068884 151068881 151068884 AGCAGCTGCTGGGCGCGGTGGCTCATGCCTATAATCCCAGCACCTTGGGAGGCTGAGGTGGGTGG AGCAGCTGCTGGGCGCGGTGGCTCATGCCT___ATCCCAGCACCTTGGGAGGCTGAGGTGGGTGG TATA T SLC4A2 Ensembl:ENSG00000164889 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1420011232 Functional Loss DEL dbSNP153 31..33 33 - - - RMVar_hsa_circ_91308,RMVar_hsa_circ_100849,RMVar_hsa_circ_249416,RMVar_hsa_circ_108385,RMVar_hsa_circ_249417,RMVar_hsa_circ_249418 25258 RMVar_ID_25258 Human_SNP_ID_345211596 A-to-I Human chr7 + 151068882 151068882 151068882 GAAGCAGCTGCTGGGCGCGGTGGCTCATGCCTATAATCCCAGCACCTTGGGAGGCTGAGGTGGGT GAAGCAGCTGCTGGGCGCGGTGGCTCATGCCTGTAATCCCAGCACCTTGGGAGGCTGAGGTGGGT A G SLC4A2 Ensembl:ENSG00000164889 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs751382429 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91308,RMVar_hsa_circ_100849,RMVar_hsa_circ_249416,RMVar_hsa_circ_108385,RMVar_hsa_circ_249417,RMVar_hsa_circ_249418 25259 RMVar_ID_25259 Human_SNP_ID_345215554 A-to-I Human chr7 - 151080300 151080300 151080300 GAGAGTGCACGCCGGTGCCGCCTGGGCTCCAGACTGGGCGCGACCACTAACCCGGTTAATGACCT GAGAGTGCACGCCGGTGCCGCCTGGGCTCCAGTCTGGGCGCGACCACTAACCCGGTTAATGACCT T A FASTK Ensembl:ENSG00000164896 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1005794719 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_85496,Human_RBP_ID_253703,Human_RBP_ID_678885,Human_RBP_ID_8149676,Human_RBP_ID_9338082,Human_RBP_ID_9439431,Human_RBP_ID_18504317,Human_RBP_ID_26765105,Human_RBP_ID_26794036 Human_Splice_Rec_938261 RMVar_hsa_circ_76598,RMVar_hsa_circ_249421 25260 RMVar_ID_25260 Human_SNP_ID_345215599 A-to-I Human chr7 - 151080451 151080451 151080451 GAGGAGACTTAGAGAGACGAAGCCACTTGTCCAAGGTCACGCCGCTGGTGAGTGGGAGCGCCCAG GAGGAGACTTAGAGAGACGAAGCCACTTGTCCGAGGTCACGCCGCTGGTGAGTGGGAGCGCCCAG T C FASTK Ensembl:ENSG00000164896 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1393534322 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18504318 Human_Splice_Rec_938409 RMVar_hsa_circ_76598,RMVar_hsa_circ_249421 25261 RMVar_ID_25261 Human_SNP_ID_345215615 A-to-I Human chr7 - 151080489 151080489 151080489 GCCCTGCGAGGTGGGCGCTGCGTTTTCATTTCACGGGTGAGGAGACTTAGAGAGACGAAGCCACT GCCCTGCGAGGTGGGCGCTGCGTTTTCATTTCGCGGGTGAGGAGACTTAGAGAGACGAAGCCACT T C FASTK Ensembl:ENSG00000164896 Protein coding intron GSE100210;GSE107867;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;ASD brains,frontal_cortex - 29129909,30559470,30559470 RNA-Seq:(High) rs1029553089 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1051164,Human_RBP_ID_1683598,Human_RBP_ID_3860864,Human_RBP_ID_3971576,Human_RBP_ID_4961267,Human_RBP_ID_7711887,Human_RBP_ID_16067865,Human_RBP_ID_18095590,Human_RBP_ID_22319376 Human_Splice_Rec_938409 RMVar_hsa_circ_76598,RMVar_hsa_circ_249421 25262 RMVar_ID_25262 Human_SNP_ID_345221712 A-to-I Human chr7 + 151102634 151102634 151102634 AAAAAAAAAAAAAATTTCTTTTTTTTTGAGACAGGGTCTCGCTCTGTGGCTCAGGCTGGAGCGCA AAAAAAAAAAAAAATTTCTTTTTTTTTGAGACGGGGTCTCGCTCTGTGGCTCAGGCTGGAGCGCA A G AGAP3 Ensembl:ENSG00000133612 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1563438410 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3071346,Human_RBP_ID_17577641 RMVar_hsa_circ_249424,RMVar_hsa_circ_105264,RMVar_hsa_circ_109116,RMVar_hsa_circ_249425 25263 RMVar_ID_25263 Human_SNP_ID_345318985 A-to-I Human chr7 - 151466613 151466613 151466613 GCTTCAGGAAGGCCCCAGGTTGGATTCCAGAAACCAGTGAAGATGTGGCCACAGGAGGAGGTGTG GCTTCAGGAAGGCCCCAGGTTGGATTCCAGAAGCCAGTGAAGATGTGGCCACAGGAGGAGGTGTG T C RHEB Ensembl:ENSG00000106615 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs985543580 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_679154,Human_RBP_ID_1683693,Human_RBP_ID_3071625,Human_RBP_ID_24200061 Human_miRNA_ID_2674796,Human_miRNA_ID_2925549 RMVar_hsa_circ_249458,RMVar_hsa_circ_378075 25264 RMVar_ID_25264 Human_SNP_ID_345321953 A-to-I Human chr7 - 151479493 151479493 151479493 TATTTTGAGTGGAGACGGGGTTTCACTGTGTTAGCCAGGATGATATGAATCTCCTGACCTTGTGA TATTTTGAGTGGAGACGGGGTTTCACTGTGTTTGCCAGGATGATATGAATCTCCTGACCTTGTGA T A RHEB Ensembl:ENSG00000106615 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs994737252 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110273,RMVar_hsa_circ_249458,RMVar_hsa_circ_378075,RMVar_hsa_circ_293845,RMVar_hsa_circ_347746,RMVar_hsa_circ_249459,RMVar_hsa_circ_107775,RMVar_hsa_circ_249460,RMVar_hsa_circ_278569,RMVar_hsa_circ_249461,RMVar_hsa_circ_276140,RMVar_hsa_circ_249462,RMVar_hsa_circ_249463 25265 RMVar_ID_25265 Human_SNP_ID_345321954 A-to-I Human chr7 - 151479493 151479493 151479493 TATTTTGAGTGGAGACGGGGTTTCACTGTGTTAGCCAGGATGATATGAATCTCCTGACCTTGTGA TATTTTGAGTGGAGACGGGGTTTCACTGTGTTGGCCAGGATGATATGAATCTCCTGACCTTGTGA T C RHEB Ensembl:ENSG00000106615 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs994737252 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110273,RMVar_hsa_circ_249458,RMVar_hsa_circ_378075,RMVar_hsa_circ_293845,RMVar_hsa_circ_347746,RMVar_hsa_circ_249459,RMVar_hsa_circ_107775,RMVar_hsa_circ_249460,RMVar_hsa_circ_278569,RMVar_hsa_circ_249461,RMVar_hsa_circ_276140,RMVar_hsa_circ_249462,RMVar_hsa_circ_249463 25266 RMVar_ID_25266 Human_SNP_ID_345327414 A-to-I Human chr7 + 151503004 151503000 151503005 TGAAGTCCTCTCCGAAGTGAAATTCATTCAAGAAAAGAAATCAATAGAACGATACTTTGATGAAA TGAAGTCCTCTCCGAAGTGAAATTCATTC_____AAGAAATCAATAGAACGATACTTTGATGAAA CAAGAA C ETF1P2 Ensembl:ENSG00000240132 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1455525790 Functional Loss DEL dbSNP153 30..34 33 - - - 25267 RMVar_ID_25267 Human_SNP_ID_345344921 A-to-I Human chr7 - 151573978 151573978 151573978 GGTCAGGAGTTGGAGACCAGCCTGGCCAACATAGTGAAACCCTGTCTCTACTAAAAATACAAAAA GGTCAGGAGTTGGAGACCAGCCTGGCCAACATGGTGAAACCCTGTCTCTACTAAAAATACAAAAA T C PRKAG2 Ensembl:ENSG00000106617 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs773837054 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_304010,RMVar_hsa_circ_18808,RMVar_hsa_circ_249473,RMVar_hsa_circ_46850,RMVar_hsa_circ_53804,RMVar_hsa_circ_19505 25268 RMVar_ID_25268 Human_SNP_ID_345496838 A-to-I Human chr7 - 152157276 152157260 152157276 TCACCCAGGCCAGATTGCAGTGGTGCAATCTCAGCTCCCTGCAATCTCTGCCTCCCAAATTCAAG TCACCCAGGCCAGATTGCAGTGGTGCAATCTC________________TGCCTCCCAAATTCAAG AGAGATTGCAGGGAGCT A KMT2C Ensembl:ENSG00000055609 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1419213688 Functional Loss DEL dbSNP153 33..48 33 - - - Human_RBP_ID_26084847 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_288027,RMVar_hsa_circ_249500,RMVar_hsa_circ_86552,RMVar_hsa_circ_119772,RMVar_hsa_circ_249501,RMVar_hsa_circ_249502,RMVar_hsa_circ_249504,RMVar_hsa_circ_96423,RMVar_hsa_circ_249506,RMVar_hsa_circ_12060,RMVar_hsa_circ_347002,RMVar_hsa_circ_266149,RMVar_hsa_circ_96153,RMVar_hsa_circ_117278,RMVar_hsa_circ_249507,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 25269 RMVar_ID_25269 Human_SNP_ID_345502106 A-to-I Human chr7 - 152176596 152176596 152176596 CTCTGCCGGCCTCCCCATCCAATCATGTGTCAAGTTTGCCTCCTTTCATAGCACCGCCTGGCCGT CTCTGCCGGCCTCCCCATCCAATCATGTGTCACGTTTGCCTCCTTTCATAGCACCGCCTGGCCGT T G KMT2C Ensembl:ENSG00000055609 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1478208996 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1037293,Human_miRNA_ID_1409459,Human_miRNA_ID_2475158,Human_miRNA_ID_2782425,Human_miRNA_ID_2785393,Human_miRNA_ID_2960944 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 25270 RMVar_ID_25270 Human_SNP_ID_345533346 A-to-I Human chr7 - 152289947 152289941 152289947 TGTCTCCTGGGTTCAAGTGATGCTCATGCCTCAGCCTCCTGAGTAGCTGGGACTATAGGCATGCA TGTCTCCTGGGTTCAAGTGATGCTCATGCCTC______CTGAGTAGCTGGGACTATAGGCATGCA GGAGGCT G KMT2C Ensembl:ENSG00000055609 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1316001205 Functional Loss DEL dbSNP153 33..38 33 - - - RMVar_hsa_circ_117278,RMVar_hsa_circ_249509,RMVar_hsa_circ_91356,RMVar_hsa_circ_249516,RMVar_hsa_circ_81032,RMVar_hsa_circ_249515,RMVar_hsa_circ_107329,RMVar_hsa_circ_249527,RMVar_hsa_circ_53773,RMVar_hsa_circ_104331,RMVar_hsa_circ_249534,RMVar_hsa_circ_119780,RMVar_hsa_circ_115080,RMVar_hsa_circ_249538,RMVar_hsa_circ_249545,RMVar_hsa_circ_74460,RMVar_hsa_circ_35876,RMVar_hsa_circ_14750,RMVar_hsa_circ_74099,RMVar_hsa_circ_98628,RMVar_hsa_circ_363165,RMVar_hsa_circ_249575,RMVar_hsa_circ_337630,RMVar_hsa_circ_340253,RMVar_hsa_circ_327162,RMVar_hsa_circ_249580,RMVar_hsa_circ_298315,RMVar_hsa_circ_102758,RMVar_hsa_circ_249585,RMVar_hsa_circ_249586,RMVar_hsa_circ_10266,RMVar_hsa_circ_120217,RMVar_hsa_circ_48929,RMVar_hsa_circ_249594,RMVar_hsa_circ_249591,RMVar_hsa_circ_249589,RMVar_hsa_circ_333270,RMVar_hsa_circ_354227,RMVar_hsa_circ_270442,RMVar_hsa_circ_101905,RMVar_hsa_circ_370527,RMVar_hsa_circ_303206,RMVar_hsa_circ_249596,RMVar_hsa_circ_89470,RMVar_hsa_circ_249597,RMVar_hsa_circ_249595,RMVar_hsa_circ_96082,RMVar_hsa_circ_301085,RMVar_hsa_circ_85738,RMVar_hsa_circ_249600,RMVar_hsa_circ_249601,RMVar_hsa_circ_249602 25271 RMVar_ID_25271 Human_SNP_ID_345533730 A-to-I Human chr7 - 152290466 152290466 152290466 GTCTCTACTAAAAATACAAAAATCAGCCGGGCATGGTAGCAGGCACCTGCAGTCCCATCTACGGG GTCTCTACTAAAAATACAAAAATCAGCCGGGCGTGGTAGCAGGCACCTGCAGTCCCATCTACGGG T C KMT2C Ensembl:ENSG00000055609 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1032833065 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16075616 RMVar_hsa_circ_117278,RMVar_hsa_circ_249509,RMVar_hsa_circ_91356,RMVar_hsa_circ_249516,RMVar_hsa_circ_81032,RMVar_hsa_circ_249515,RMVar_hsa_circ_107329,RMVar_hsa_circ_249527,RMVar_hsa_circ_53773,RMVar_hsa_circ_104331,RMVar_hsa_circ_249534,RMVar_hsa_circ_119780,RMVar_hsa_circ_115080,RMVar_hsa_circ_249538,RMVar_hsa_circ_249545,RMVar_hsa_circ_74460,RMVar_hsa_circ_35876,RMVar_hsa_circ_14750,RMVar_hsa_circ_74099,RMVar_hsa_circ_98628,RMVar_hsa_circ_363165,RMVar_hsa_circ_249575,RMVar_hsa_circ_337630,RMVar_hsa_circ_340253,RMVar_hsa_circ_327162,RMVar_hsa_circ_249580,RMVar_hsa_circ_298315,RMVar_hsa_circ_102758,RMVar_hsa_circ_249585,RMVar_hsa_circ_249586,RMVar_hsa_circ_10266,RMVar_hsa_circ_120217,RMVar_hsa_circ_48929,RMVar_hsa_circ_249594,RMVar_hsa_circ_249591,RMVar_hsa_circ_249589,RMVar_hsa_circ_333270,RMVar_hsa_circ_354227,RMVar_hsa_circ_270442,RMVar_hsa_circ_101905,RMVar_hsa_circ_370527,RMVar_hsa_circ_303206,RMVar_hsa_circ_249596,RMVar_hsa_circ_89470,RMVar_hsa_circ_249597,RMVar_hsa_circ_249595,RMVar_hsa_circ_96082,RMVar_hsa_circ_301085,RMVar_hsa_circ_85738,RMVar_hsa_circ_249600,RMVar_hsa_circ_249601,RMVar_hsa_circ_249602 25272 RMVar_ID_25272 Human_SNP_ID_345537080 A-to-I Human chr7 - 152302406 152302406 152302406 CAGCCTGGCCAATGTGATGAAACCCCCTCTCTACTAAAAATACAAAAATTAGCTTGGCATGGTGA CAGCCTGGCCAATGTGATGAAACCCCCTCTCTGCTAAAAATACAAAAATTAGCTTGGCATGGTGA T C KMT2C Ensembl:ENSG00000055609 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1048165843 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117278,RMVar_hsa_circ_249509,RMVar_hsa_circ_91356,RMVar_hsa_circ_249516,RMVar_hsa_circ_81032,RMVar_hsa_circ_249515,RMVar_hsa_circ_107329,RMVar_hsa_circ_249527,RMVar_hsa_circ_53773,RMVar_hsa_circ_104331,RMVar_hsa_circ_249534,RMVar_hsa_circ_119780,RMVar_hsa_circ_115080,RMVar_hsa_circ_249538,RMVar_hsa_circ_249545,RMVar_hsa_circ_74460,RMVar_hsa_circ_35876,RMVar_hsa_circ_14750,RMVar_hsa_circ_74099,RMVar_hsa_circ_98628,RMVar_hsa_circ_363165,RMVar_hsa_circ_249575,RMVar_hsa_circ_337630,RMVar_hsa_circ_340253,RMVar_hsa_circ_327162,RMVar_hsa_circ_249580,RMVar_hsa_circ_298315,RMVar_hsa_circ_102758,RMVar_hsa_circ_249585,RMVar_hsa_circ_249586,RMVar_hsa_circ_10266,RMVar_hsa_circ_120217,RMVar_hsa_circ_48929,RMVar_hsa_circ_249594,RMVar_hsa_circ_249591,RMVar_hsa_circ_249589,RMVar_hsa_circ_333270,RMVar_hsa_circ_354227,RMVar_hsa_circ_270442,RMVar_hsa_circ_101905,RMVar_hsa_circ_370527,RMVar_hsa_circ_303206,RMVar_hsa_circ_249596,RMVar_hsa_circ_89470,RMVar_hsa_circ_249597,RMVar_hsa_circ_249595,RMVar_hsa_circ_96082,RMVar_hsa_circ_301085,RMVar_hsa_circ_85738,RMVar_hsa_circ_249600,RMVar_hsa_circ_249601,RMVar_hsa_circ_249602 25273 RMVar_ID_25273 Human_SNP_ID_345539493 A-to-I Human chr7 - 152310823 152310823 152310823 AAAATTCCCGGAGTGTGGTGGCATGTGCCTGTAGTCCCAGCTATTTGGCAAGGCTGAGACAGGAG AAAATTCCCGGAGTGTGGTGGCATGTGCCTGTGGTCCCAGCTATTTGGCAAGGCTGAGACAGGAG T C KMT2C Ensembl:ENSG00000055609 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1394315689 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117278,RMVar_hsa_circ_249509,RMVar_hsa_circ_91356,RMVar_hsa_circ_249516,RMVar_hsa_circ_81032,RMVar_hsa_circ_249515,RMVar_hsa_circ_107329,RMVar_hsa_circ_249527,RMVar_hsa_circ_53773,RMVar_hsa_circ_104331,RMVar_hsa_circ_249534,RMVar_hsa_circ_119780,RMVar_hsa_circ_115080,RMVar_hsa_circ_249538,RMVar_hsa_circ_249545,RMVar_hsa_circ_74460,RMVar_hsa_circ_35876,RMVar_hsa_circ_14750,RMVar_hsa_circ_249604,RMVar_hsa_circ_74099,RMVar_hsa_circ_98628,RMVar_hsa_circ_363165,RMVar_hsa_circ_249575,RMVar_hsa_circ_337630,RMVar_hsa_circ_340253,RMVar_hsa_circ_327162,RMVar_hsa_circ_249580,RMVar_hsa_circ_298315,RMVar_hsa_circ_249586,RMVar_hsa_circ_10266,RMVar_hsa_circ_120217,RMVar_hsa_circ_48929,RMVar_hsa_circ_249594,RMVar_hsa_circ_249591,RMVar_hsa_circ_249589,RMVar_hsa_circ_333270,RMVar_hsa_circ_354227,RMVar_hsa_circ_270442,RMVar_hsa_circ_101905,RMVar_hsa_circ_370527,RMVar_hsa_circ_303206,RMVar_hsa_circ_249596,RMVar_hsa_circ_249595,RMVar_hsa_circ_96082,RMVar_hsa_circ_301085,RMVar_hsa_circ_81482,RMVar_hsa_circ_249601,RMVar_hsa_circ_249602,RMVar_hsa_circ_281075,RMVar_hsa_circ_288969,RMVar_hsa_circ_286663,RMVar_hsa_circ_277395,RMVar_hsa_circ_249606,RMVar_hsa_circ_249608,RMVar_hsa_circ_249609,RMVar_hsa_circ_249607,RMVar_hsa_circ_249605 25274 RMVar_ID_25274 Human_SNP_ID_345554853 A-to-I Human chr7 - 152367948 152367948 152367948 TCTGTTTTTTAAACTGTTGGCATTCCTCTGGTATAAGTGTGTCTGCTTTGGCAATAAGTTGGATG TCTGTTTTTTAAACTGTTGGCATTCCTCTGGTGTAAGTGTGTCTGCTTTGGCAATAAGTTGGATG T C KMT2C Ensembl:ENSG00000055609 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1164629468 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3072940,Human_RBP_ID_16076578,Human_RBP_ID_24439830 RMVar_hsa_circ_249604,RMVar_hsa_circ_101905,RMVar_hsa_circ_249595,RMVar_hsa_circ_81482 25275 RMVar_ID_25275 Human_SNP_ID_345554984 A-to-I Human chr7 + 152368466 152368466 152368466 GAGATGAAGGTCAAATAAAAAGTTCAAAAACTAAAGGACTCTGAAGCTGAGCTCCAGTGGCGCCG GAGATGAAGGTCAAATAAAAAGTTCAAAAACTGAAGGACTCTGAAGCTGAGCTCCAGTGGCGCCG A G SEPTIN7P6 Ensembl:ENSG00000241007 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1472011481 Functional Loss SNV dbSNP153 33..33 33 - - - 25276 RMVar_ID_25276 Human_SNP_ID_345564698 A-to-I Human chr7 - 152405908 152405908 152405908 ATGATCTTGACTCACTGCAACCTCTGCCTCCCAGGTTCAAGCGATTCTCCTCCCTCGGCCTCCCG ATGATCTTGACTCACTGCAACCTCTGCCTCCCTGGTTCAAGCGATTCTCCTCCCTCGGCCTCCCG T A KMT2C Ensembl:ENSG00000055609 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1410722000 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_249604,RMVar_hsa_circ_101905,RMVar_hsa_circ_249595,RMVar_hsa_circ_81482 25277 RMVar_ID_25277 Human_SNP_ID_345565598 A-to-I Human chr7 - 152409137 152409137 152409137 CCAGGTGTGATGGCACATTCTTGTGTGATCCCAGCTAATCGGGAGGCTGAGGTGGAAGGATCAGG CCAGGTGTGATGGCACATTCTTGTGTGATCCCGGCTAATCGGGAGGCTGAGGTGGAAGGATCAGG T C KMT2C Ensembl:ENSG00000055609 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1014915104 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17578008 RMVar_hsa_circ_249604,RMVar_hsa_circ_101905,RMVar_hsa_circ_249595,RMVar_hsa_circ_81482 25278 RMVar_ID_25278 Human_SNP_ID_345565621 A-to-I Human chr7 - 152409206 152409206 152409206 GGTAAGGCGTTCAAGACCAGCCTGGACAACATAGTGAGACCCTGACCCTAAAAAAAATACAAAAA GGTAAGGCGTTCAAGACCAGCCTGGACAACATGGTGAGACCCTGACCCTAAAAAAAATACAAAAA T C KMT2C Ensembl:ENSG00000055609 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1488634311 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16077121 RMVar_hsa_circ_249604,RMVar_hsa_circ_101905,RMVar_hsa_circ_249595,RMVar_hsa_circ_81482 25279 RMVar_ID_25279 Human_SNP_ID_345566034 A-to-I Human chr7 - 152410385 152410385 152410385 TTTTTTGAGACAGGGTCTTCCTCCGTCGCCCAAGCTGGAGTGCGAGGGCGCGATCTTGACTCAGT TTTTTTGAGACAGGGTCTTCCTCCGTCGCCCAGGCTGGAGTGCGAGGGCGCGATCTTGACTCAGT T C KMT2C Ensembl:ENSG00000055609 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404176071 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_249604,RMVar_hsa_circ_101905,RMVar_hsa_circ_249595,RMVar_hsa_circ_81482 25280 RMVar_ID_25280 Human_SNP_ID_345569175 A-to-I Human chr7 - 152419307 152419307 152419307 TCGCTCTGTTGCCCAGGCTGGAGCCCAGTGGCATGATCTCGGCTCACTGCAATCTCCGCCTCCCG TCGCTCTGTTGCCCAGGCTGGAGCCCAGTGGCTTGATCTCGGCTCACTGCAATCTCCGCCTCCCG T A KMT2C Ensembl:ENSG00000055609 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1363000116 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_249604,RMVar_hsa_circ_101905,RMVar_hsa_circ_249595,RMVar_hsa_circ_81482 25281 RMVar_ID_25281 Human_SNP_ID_345569176 A-to-I Human chr7 - 152419307 152419307 152419307 TCGCTCTGTTGCCCAGGCTGGAGCCCAGTGGCATGATCTCGGCTCACTGCAATCTCCGCCTCCCG TCGCTCTGTTGCCCAGGCTGGAGCCCAGTGGCGTGATCTCGGCTCACTGCAATCTCCGCCTCCCG T C KMT2C Ensembl:ENSG00000055609 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1363000116 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_249604,RMVar_hsa_circ_101905,RMVar_hsa_circ_249595,RMVar_hsa_circ_81482 25282 RMVar_ID_25282 Human_SNP_ID_345572174 A-to-I Human chr7 - 152430663 152430663 152430663 GCTGGGTGTGGTGGTAGGCACCTGTAGTCCCAACTACTCTGGAGACTGAGCTGAGAGAAGATTGT GCTGGGTGTGGTGGTAGGCACCTGTAGTCCCAGCTACTCTGGAGACTGAGCTGAGAGAAGATTGT T C KMT2C Ensembl:ENSG00000055609 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1257575965 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_249604,RMVar_hsa_circ_101905,RMVar_hsa_circ_249595,RMVar_hsa_circ_81482 25283 RMVar_ID_25283 Human_SNP_ID_345572185 A-to-I Human chr7 - 152430726 152430726 152430726 TTTAAAAGGAGTTTGAGACCAGCCTGGGCAACAAAGTGAGGCCTTGTCTCTACAAAAAAATTAGC TTTAAAAGGAGTTTGAGACCAGCCTGGGCAACGAAGTGAGGCCTTGTCTCTACAAAAAAATTAGC T C KMT2C Ensembl:ENSG00000055609 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1378160672 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_249604,RMVar_hsa_circ_101905,RMVar_hsa_circ_249595,RMVar_hsa_circ_81482 25284 RMVar_ID_25284 Human_SNP_ID_345572828 A-to-I Human chr7 - 152433104 152433104 152433104 TTGCTCTGTAGCCCAGGCTGTAGTGCAGTGGTATGATCTCGGCTCACCGCAACCTCTGCCTCGTG TTGCTCTGTAGCCCAGGCTGTAGTGCAGTGGTGTGATCTCGGCTCACCGCAACCTCTGCCTCGTG T C KMT2C Ensembl:ENSG00000055609 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1246068719 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16077748,Human_RBP_ID_21463836 RMVar_hsa_circ_249604,RMVar_hsa_circ_101905,RMVar_hsa_circ_249595,RMVar_hsa_circ_81482 25285 RMVar_ID_25285 Human_SNP_ID_345630329 A-to-I Human chr7 - 152641784 152641784 152641784 GGGCATGGTGGTGCATACCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATAACTTGAA GGGCATGGTGGTGCATACCTGTAATCCCAGCTGCTCGGGAGGCTGAGGCAGGAGAATAACTTGAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459589355 Functional Loss SNV dbSNP153 33..33 33 - - - 25286 RMVar_ID_25286 Human_SNP_ID_345630337 A-to-I Human chr7 - 152641833 152641833 152641833 CTGACCAATATGGTGAAACTCCATCTCTAGTAAAAATACAAAATTAGGTGGGCATGGTGGTGCAT CTGACCAATATGGTGAAACTCCATCTCTAGTACAAATACAAAATTAGGTGGGCATGGTGGTGCAT T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs536017624 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23074086 25287 RMVar_ID_25287 Human_SNP_ID_345630595 A-to-I Human chr7 - 152642645 152642645 152642645 CAGAGTCTCGCTCTGACGCCAGGCTGGAGTGCAGTGGCGTGATCTCGGCTCACCGCAACCTCCGC CAGAGTCTCGCTCTGACGCCAGGCTGGAGTGCGGTGGCGTGATCTCGGCTCACCGCAACCTCCGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1014074576 Functional Loss SNV dbSNP153 33..33 33 - - - 25288 RMVar_ID_25288 Human_SNP_ID_345631509 A-to-I Human chr7 - 152645855 152645855 152645855 GGCTGGAGTGCAGTGGCATCATAACTCACTGCAGCCTCGAACTCCTGGGTTCCAGTGAGCCTCCA GGCTGGAGTGCAGTGGCATCATAACTCACTGCGGCCTCGAACTCCTGGGTTCCAGTGAGCCTCCA T C XRCC2 Ensembl:ENSG00000196584 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1310911684 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16077985,Human_RBP_ID_26086354,Human_RBP_ID_27108919 25289 RMVar_ID_25289 Human_SNP_ID_345631529 A-to-I Human chr7 - 152645914 152645914 152645914 TTTTTAAAATACATATTTGCTGTTTTATTTTTAGAGACAAGGTCTCGCTCCGTTGCCCAGGCTGG TTTTTAAAATACATATTTGCTGTTTTATTTTTCGAGACAAGGTCTCGCTCCGTTGCCCAGGCTGG T G XRCC2 Ensembl:ENSG00000196584 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229,31158229 RNA-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 25290 RMVar_ID_25290 Human_SNP_ID_345631769 A-to-I Human chr7 - 152646615 152646615 152646615 AAAATTAGCTGGGCATGGTGGTGCGTGCCTGTAGTGCCAGCTACTCAGGAGGCCGAGGCAGGAGA AAAATTAGCTGGGCATGGTGGTGCGTGCCTGTGGTGCCAGCTACTCAGGAGGCCGAGGCAGGAGA T C XRCC2 Ensembl:ENSG00000196584 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs978623244 Functional Loss SNV dbSNP153 33..33 33 - - - 25291 RMVar_ID_25291 Human_SNP_ID_345632154 A-to-I Human chr7 - 152648241 152648241 152648241 CACCACGCCTGGCTAATTTTTGTATTTTTAATAGAGACGGGGTTTCACCATGTTGGCCAGGCTGG CACCACGCCTGGCTAATTTTTGTATTTTTAATGGAGACGGGGTTTCACCATGTTGGCCAGGCTGG T C XRCC2 Ensembl:ENSG00000196584 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs368068919 Functional Loss SNV dbSNP153 33..33 33 - - - 25292 RMVar_ID_25292 Human_SNP_ID_345632168 A-to-I Human chr7 - 152648285 152648285 152648285 CTTCCACCTCAGCCTCCCAGGTAGCTGGGATTACAGGCACCCACCACCACGCCTGGCTAATTTTT CTTCCACCTCAGCCTCCCAGGTAGCTGGGATTGCAGGCACCCACCACCACGCCTGGCTAATTTTT T C XRCC2 Ensembl:ENSG00000196584 Protein coding 3'UTR GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs1246585181 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24201093,Human_RBP_ID_27108966 Human_miRNA_ID_605394,Human_miRNA_ID_1400721 25293 RMVar_ID_25293 Human_SNP_ID_345632174 A-to-I Human chr7 - 152648299 152648299 152648299 GGGTTCAAGTGATTCTTCCACCTCAGCCTCCCAGGTAGCTGGGATTACAGGCACCCACCACCACG GGGTTCAAGTGATTCTTCCACCTCAGCCTCCCGGGTAGCTGGGATTACAGGCACCCACCACCACG T C XRCC2 Ensembl:ENSG00000196584 Protein coding 3'UTR GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs1280998583 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24201093,Human_RBP_ID_27108966 25294 RMVar_ID_25294 Human_SNP_ID_345633123 A-to-I Human chr7 - 152651684 152651684 152651684 CATGGTGGAACCCAGTCTTTACAAGAAATACAAAAATTAGCCAGGCATGATGACACATGCCTGTA CATGGTGGAACCCAGTCTTTACAAGAAATACAGAAATTAGCCAGGCATGATGACACATGCCTGTA T C XRCC2 Ensembl:ENSG00000196584 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1290760546 Functional Loss SNV dbSNP153 33..33 33 - - - 25295 RMVar_ID_25295 Human_SNP_ID_345633135 A-to-I Human chr7 - 152651732 152651732 152651732 AGGCAGGCAGACCACTTGAGCCCAGGAGTTCAAGACCAGCCTGGGCAACATGGTGGAACCCAGTC AGGCAGGCAGACCACTTGAGCCCAGGAGTTCAGGACCAGCCTGGGCAACATGGTGGAACCCAGTC T C XRCC2 Ensembl:ENSG00000196584 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs950212294 Functional Loss SNV dbSNP153 33..33 33 - - - 25296 RMVar_ID_25296 Human_SNP_ID_345633595 A-to-I Human chr7 - 152653737 152653737 152653737 CTACTTTGGGTTGGGTGTGGTGGTGCATGCCTATAAGTCTAGCACTTTGGGAGGCTGAGGTAGGT CTACTTTGGGTTGGGTGTGGTGGTGCATGCCTGTAAGTCTAGCACTTTGGGAGGCTGAGGTAGGT T C XRCC2 Ensembl:ENSG00000196584 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1346819235 Functional Loss SNV dbSNP153 33..33 33 - - - 25297 RMVar_ID_25297 Human_SNP_ID_345635051 A-to-I Human chr7 - 152660103 152660103 152660103 GCTCTAGGCAACTACTAATCTACTTTCTAACTATGGATTTGCCTTTTCTGGACATTTCATATAAT GCTCTAGGCAACTACTAATCTACTTTCTAACTGTGGATTTGCCTTTTCTGGACATTTCATATAAT T C XRCC2 Ensembl:ENSG00000196584 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1283957180 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8662396,Human_RBP_ID_18095968 25298 RMVar_ID_25298 Human_SNP_ID_345635307 A-to-I Human chr7 - 152661052 152661050 152661053 TCAAGTGATCTTCCCACCTCAGCCTCCTCAGTAGCTGGGATTACAGTGTGTGCCACCATGCCCAG TCAAGTGATCTTCCCACCTCAGCCTCCTCAG___CTGGGATTACAGTGTGTGCCACCATGCCCAG GCTA G XRCC2 Ensembl:ENSG00000196584 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1016577391 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_26086465 25299 RMVar_ID_25299 Human_SNP_ID_345635566 A-to-I Human chr7 - 152662266 152662266 152662266 AACCACCAAGATGATCTGTTTGAAATGCAGATAGGCTGGGCGCGGTGGCTCACGCCTGTAATCCC AACCACCAAGATGATCTGTTTGAAATGCAGATGGGCTGGGCGCGGTGGCTCACGCCTGTAATCCC T C XRCC2 Ensembl:ENSG00000196584 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1296258925 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16078416 25300 RMVar_ID_25300 Human_SNP_ID_345636696 A-to-I Human chr7 - 152666463 152666463 152666463 TCATGCTTGTAATCCCAGCACTTTGGGAGGCTAAGGTGGGAGAACTGCTTGAGTCCAGGAGTTCG TCATGCTTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGAGAACTGCTTGAGTCCAGGAGTTCG T C XRCC2 Ensembl:ENSG00000196584 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1053843527 Functional Loss SNV dbSNP153 33..33 33 - - - 25301 RMVar_ID_25301 Human_SNP_ID_345637758 A-to-I Human chr7 - 152670800 152670800 152670800 GATTACCTGAGTTCGAGACCAGCCTGACCAACATGGCAAAACCCTGTCTCTACTAAAAATACAAA GATTACCTGAGTTCGAGACCAGCCTGACCAACGTGGCAAAACCCTGTCTCTACTAAAAATACAAA T C XRCC2 Ensembl:ENSG00000196584 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1422708086 Functional Loss SNV dbSNP153 33..33 33 - - - 25302 RMVar_ID_25302 Human_SNP_ID_345638318 A-to-I Human chr7 - 152673431 152673431 152673431 GCTGGGTGCAGTGGCTCATGCCCGTAATCCCAACACTTTGGGAGGTTGAGGTGGGCAGATCACCT GCTGGGTGCAGTGGCTCATGCCCGTAATCCCAGCACTTTGGGAGGTTGAGGTGGGCAGATCACCT T C XRCC2 Ensembl:ENSG00000196584 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs900155688 Functional Loss SNV dbSNP153 33..33 33 - - - 25303 RMVar_ID_25303 Human_SNP_ID_345638386 A-to-I Human chr7 - 152673754 152673754 152673754 CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGTGCACGCCACCATGCCCGGCTAATTTAT CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTGCAGGTGCACGCCACCATGCCCGGCTAATTTAT T C XRCC2 Ensembl:ENSG00000196584 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs965859533 Functional Loss SNV dbSNP153 33..33 33 - - - 25304 RMVar_ID_25304 Human_SNP_ID_345666005 A-to-I Human chr7 + 152771043 152771043 152771043 TGGAGTGCAGTGGCTTGATCTCGGCTTACTGCAACCTCTGCCTCCTGGGTTTAAGCCATTCTCCT TGGAGTGCAGTGGCTTGATCTCGGCTTACTGCGACCTCTGCCTCCTGGGTTTAAGCCATTCTCCT A G ACTR3B Ensembl:ENSG00000133627 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417158010 Functional Loss SNV dbSNP153 33..33 33 - - - 25305 RMVar_ID_25305 Human_SNP_ID_345667750 A-to-I Human chr7 + 152778447 152778447 152778447 TAGTATAGAGATGGGGTTTTACCATTTTGCCCAGGGTGGTCTTGAACTCCTGAGCTCAGGTGATC TAGTATAGAGATGGGGTTTTACCATTTTGCCCGGGGTGGTCTTGAACTCCTGAGCTCAGGTGATC A G ACTR3B Ensembl:ENSG00000133627 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1052815033 Functional Loss SNV dbSNP153 33..33 33 - - - 25306 RMVar_ID_25306 Human_SNP_ID_345694171 A-to-I Human chr7 + 152881614 152881614 152881614 CTCCCACTTCAGCCTCCCAAGTAGCTGGGATCACAGATATGTGCCACCACACCCAGCTAAGTTTT CTCCCACTTCAGCCTCCCAAGTAGCTGGGATCGCAGATATGTGCCACCACACCCAGCTAAGTTTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs994497357 Functional Loss SNV dbSNP153 33..33 33 - - - 25307 RMVar_ID_25307 Human_SNP_ID_345957954 A-to-I Human chr7 + 153902947 153902947 153902947 TTTCAACAGGAAGAAGTAAGTGTCTTATTTCTAGCTTGTATTAGTCCTTACAAGCCAGAGCATTC TTTCAACAGGAAGAAGTAAGTGTCTTATTTCTGGCTTGTATTAGTCCTTACAAGCCAGAGCATTC A G DPP6 Ensembl:ENSG00000130226 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs748312686 Functional Loss SNV dbSNP153 33..33 33 - - - 25308 RMVar_ID_25308 Human_SNP_ID_346014729 A-to-I Human chr7 + 154101731 154101731 154101731 GGGCGGATCACCTGAGGTCAGGAGTTGTAGACAAGCCTGGTCAACATGGTGAAACCCCATCTCTA GGGCGGATCACCTGAGGTCAGGAGTTGTAGACGAGCCTGGTCAACATGGTGAAACCCCATCTCTA A G DPP6 Ensembl:ENSG00000130226 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1379325083 Functional Loss SNV dbSNP153 33..33 33 - - - 25309 RMVar_ID_25309 Human_SNP_ID_346034409 A-to-I Human chr7 + 154180256 154180256 154180256 TATAATCTCAGCTACTCGGGAGGCTGAGGCATAAGAATCGCATGAACCCGGGAGGTGGAGGCTGC TATAATCTCAGCTACTCGGGAGGCTGAGGCATGAGAATCGCATGAACCCGGGAGGTGGAGGCTGC A G DPP6 Ensembl:ENSG00000130226 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs544620341 Functional Loss SNV dbSNP153 33..33 33 - - - 25310 RMVar_ID_25310 Human_SNP_ID_346050698 A-to-I Human chr7 + 154243684 154243684 154243684 GGGCATGGTGGCGGGTGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATGATGTGAA GGGCATGGTGGCGGGTGCCTGTAGTCCCAGCTGCTCAGGAGGCTGAGGCAGGAGAATGATGTGAA A G DPP6 Ensembl:ENSG00000130226 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1397921943 Functional Loss SNV dbSNP153 33..33 33 - - - 25311 RMVar_ID_25311 Human_SNP_ID_346061424 A-to-I Human chr7 + 154285439 154285439 154285439 GGCACCCGCCACCACACTTGGCTAATGTTTGCATTATTAGTAGAGACGGGGTTTCACCGTGTTGG GGCACCCGCCACCACACTTGGCTAATGTTTGCCTTATTAGTAGAGACGGGGTTTCACCGTGTTGG A C DPP6 Ensembl:ENSG00000130226 Protein coding intron GSE47997;GSE107867 K562 cells&HepG2 cells;ASD brains,cerebellum - 23474544,30559470 RNA-Seq:(High) rs575175920 Functional Loss SNV dbSNP153 33..33 33 - - - 25312 RMVar_ID_25312 Human_SNP_ID_346061425 A-to-I Human chr7 + 154285439 154285439 154285439 GGCACCCGCCACCACACTTGGCTAATGTTTGCATTATTAGTAGAGACGGGGTTTCACCGTGTTGG GGCACCCGCCACCACACTTGGCTAATGTTTGCGTTATTAGTAGAGACGGGGTTTCACCGTGTTGG A G DPP6 Ensembl:ENSG00000130226 Protein coding intron GSE47997;GSE107867 K562 cells&HepG2 cells;ASD brains,cerebellum - 23474544,30559470 RNA-Seq:(High) rs575175920 Functional Loss SNV dbSNP153 33..33 33 - - - 25313 RMVar_ID_25313 Human_SNP_ID_346085523 A-to-I Human chr7 + 154378805 154378805 154378805 TGGGGAAGCCTCAGGAAACTTACAATCAAGGCAGAAGGCAAAGGAGAACCAGGCAACTTCTTCGC TGGGGAAGCCTCAGGAAACTTACAATCAAGGCGGAAGGCAAAGGAGAACCAGGCAACTTCTTCGC A G DPP6 Ensembl:ENSG00000130226 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs879202695 Functional Loss SNV dbSNP153 33..33 33 - - - 25314 RMVar_ID_25314 Human_SNP_ID_346216257 A-to-I Human chr7 + 154891124 154891124 154891124 GTAGTCATGTGTACCTGTGGTCCCAGCTACACAGGAGGCTGAAGTGGGAGAATCACTTGAGCCCA GTAGTCATGTGTACCTGTGGTCCCAGCTACACGGGAGGCTGAAGTGGGAGAATCACTTGAGCCCA A G DPP6 Ensembl:ENSG00000130226 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs550158294 Functional Loss SNV dbSNP153 33..33 33 - - - 25315 RMVar_ID_25315 Human_SNP_ID_346216682 A-to-I Human chr7 - 154892597 154892597 154892597 AAACTGCCTTCCGCATCCGAGACACACATGCTATGGAACACCCGGCCCCGCCCCGCCCCGCCCCT AAACTGCCTTCCGCATCCGAGACACACATGCTGTGGAACACCCGGCCCCGCCCCGCCCCGCCCCT T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1041888139 Functional Loss SNV dbSNP153 33..33 33 - - - 25316 RMVar_ID_25316 Human_SNP_ID_346237993 A-to-I Human chr7 - 154980535 154980535 154980535 TGACTCACGCCTGTGGTCCTAGCTACTTGGGAAGCTGAGACGGAAGGATTGCTTGAGCCTGGGAG TGACTCACGCCTGTGGTCCTAGCTACTTGGGAGGCTGAGACGGAAGGATTGCTTGAGCCTGGGAG T C PAXIP1 Ensembl:ENSG00000157212 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1484634783 Functional Loss SNV dbSNP153 33..33 33 - - - 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_95345,RMVar_hsa_circ_86230,RMVar_hsa_circ_249652,RMVar_hsa_circ_249653,RMVar_hsa_circ_287023,RMVar_hsa_circ_278003,RMVar_hsa_circ_249655,RMVar_hsa_circ_358546,RMVar_hsa_circ_21758,RMVar_hsa_circ_331292,RMVar_hsa_circ_290565 25317 RMVar_ID_25317 Human_SNP_ID_346244131 A-to-I Human chr7 + 155004339 155004339 155004339 CGCGGTGGCTCACGCCTGTAATCCTATCCTTTAGGAGGCCGAGGTGGGCGGATTGCCTGAGTTCA CGCGGTGGCTCACGCCTGTAATCCTATCCTTTGGGAGGCCGAGGTGGGCGGATTGCCTGAGTTCA A G PAXIP1-AS1 Ensembl:ENSG00000273344 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs11552216 Functional Loss SNV dbSNP153 33..33 33 - - - 25318 RMVar_ID_25318 Human_SNP_ID_346244172 A-to-I Human chr7 + 155004474 155004474 155004474 GTGGCGGCACGCGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATGGCTTGAACTCG GTGGCGGCACGCGCCTGTAGTCCCAGCTACTCCGGAGGCTGAGGCAGGAGAATGGCTTGAACTCG A C PAXIP1-AS1 Ensembl:ENSG00000273344 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs889570493 Functional Loss SNV dbSNP153 33..33 33 - - - 25319 RMVar_ID_25319 Human_SNP_ID_346244197 A-to-I Human chr7 + 155004522 155004522 155004522 AGAATGGCTTGAACTCGGGTGGGGGAGGTTGCAATGAGCCGAGATCGCGCCGCTGCACTCCAGCC AGAATGGCTTGAACTCGGGTGGGGGAGGTTGCCATGAGCCGAGATCGCGCCGCTGCACTCCAGCC A C PAXIP1-AS1 Ensembl:ENSG00000273344 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934041554 Functional Loss SNV dbSNP153 33..33 33 - - - 25320 RMVar_ID_25320 Human_SNP_ID_346244575 A-to-I Human chr7 + 155005945 155005945 155005945 TTTAGTAGAGACAGGTTTTCACTATGTTGGCCAGGCTGGTCTTGAACTCCTGACCTTGTGATCCT TTTAGTAGAGACAGGTTTTCACTATGTTGGCCGGGCTGGTCTTGAACTCCTGACCTTGTGATCCT A G PAXIP1-AS1,PAXIP1-AS1:2,PAXIP1-AS1:3,PAXIP1-AS1:4,PAXIP1-AS1:5,PAXIP1-AS1:6 RNACentral:URS00009BD226,RNACentral:URS0000D582FD,RNACentral:URS0000D5CE21,RNACentral:URS0000D5CDC2,RNACentral:URS00009B34B3,RNACentral:URS00008C3ADC lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,exon,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1241949833 Functional Loss SNV dbSNP153 33..33 33 - - - 25321 RMVar_ID_25321 Human_SNP_ID_346459391 A-to-I Human chr7 + 155780056 155780056 155780056 CAGGTACTATTGTAATGTATTCTGTATTTAATAATTTAATATACTCTAGAAAGTAGACCTCATGC CAGGTACTATTGTAATGTATTCTGTATTTAATGATTTAATATACTCTAGAAAGTAGACCTCATGC A G RBM33 Ensembl:ENSG00000184863 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1159335388 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2038431,Human_RBP_ID_7786727,Human_RBP_ID_9208201,Human_RBP_ID_10342385,Human_RBP_ID_17047707 RMVar_hsa_circ_108904,RMVar_hsa_circ_249684,RMVar_hsa_circ_127344,RMVar_hsa_circ_249685,RMVar_hsa_circ_112913,RMVar_hsa_circ_249696 25322 RMVar_ID_25322 Human_SNP_ID_346712298 A-to-I Human chr7 - 156728972 156728972 156728972 AGCCAGGCATGGTGGCATGTATCTGTAGTCCCAGCTACTTGGGTGGTTGAGATGGGAGGATCACT AGCCAGGCATGGTGGCATGTATCTGTAGTCCCGGCTACTTGGGTGGTTGAGATGGGAGGATCACT T C LMBR1 Ensembl:ENSG00000105983 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1201349143 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6333,RMVar_hsa_circ_51769,RMVar_hsa_circ_369210,RMVar_hsa_circ_32072,RMVar_hsa_circ_19847,RMVar_hsa_circ_279278,RMVar_hsa_circ_321926,RMVar_hsa_circ_249725,RMVar_hsa_circ_371277,RMVar_hsa_circ_378238,RMVar_hsa_circ_123821,RMVar_hsa_circ_249724,RMVar_hsa_circ_337120,RMVar_hsa_circ_286930,RMVar_hsa_circ_310790,RMVar_hsa_circ_285312,RMVar_hsa_circ_276355,RMVar_hsa_circ_36935,RMVar_hsa_circ_249727,RMVar_hsa_circ_249729,RMVar_hsa_circ_249731,RMVar_hsa_circ_249732,RMVar_hsa_circ_249730,RMVar_hsa_circ_249728,RMVar_hsa_circ_75283,RMVar_hsa_circ_249726,RMVar_hsa_circ_293118,RMVar_hsa_circ_53261,RMVar_hsa_circ_249736,RMVar_hsa_circ_249735,RMVar_hsa_circ_363625 25323 RMVar_ID_25323 Human_SNP_ID_346770894 A-to-I Human chr7 + 156957564 156957564 156957564 TTGGGAGGCCGAGGCGGGTGGATCATGAGGTCAGGAGATTGAGACCATCCTGGCTAACATGGTGA TTGGGAGGCCGAGGCGGGTGGATCATGAGGTCGGGAGATTGAGACCATCCTGGCTAACATGGTGA A G NOM1 Ensembl:ENSG00000146909 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs929543659 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102460,RMVar_hsa_circ_249759,RMVar_hsa_circ_17535 25324 RMVar_ID_25324 Human_SNP_ID_346774828 A-to-I Human chr7 + 156970126 156970125 156970126 CCTGGGCAAAACCCTGTCTCTACTAAAAATATAAAAATTAGCCAGGCATGATGGCACATGCTGGT CCTGGGCAAAACCCTGTCTCTACTAAAAATAT_AAAATTAGCCAGGCATGATGGCACATGCTGGT TA T NOM1 Ensembl:ENSG00000146909 Protein coding 3'UTR GSE100210;GSE99789 HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 29129909,29796672 RNA-Seq:(High) rs201149415 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_106494,RMVar_hsa_circ_249760,RMVar_hsa_circ_84383,RMVar_hsa_circ_249767 25325 RMVar_ID_25325 Human_SNP_ID_346774829 A-to-I Human chr7 + 156970126 156970126 156970126 CCTGGGCAAAACCCTGTCTCTACTAAAAATATAAAAATTAGCCAGGCATGATGGCACATGCTGGT CCTGGGCAAAACCCTGTCTCTACTAAAAATATCAAAATTAGCCAGGCATGATGGCACATGCTGGT A C NOM1 Ensembl:ENSG00000146909 Protein coding 3'UTR GSE100210;GSE99789 HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 29129909,29796672 RNA-Seq:(High) rs1439039685 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106494,RMVar_hsa_circ_249760,RMVar_hsa_circ_84383,RMVar_hsa_circ_249767 25326 RMVar_ID_25326 Human_SNP_ID_346774830 A-to-I Human chr7 + 156970126 156970126 156970126 CCTGGGCAAAACCCTGTCTCTACTAAAAATATAAAAATTAGCCAGGCATGATGGCACATGCTGGT CCTGGGCAAAACCCTGTCTCTACTAAAAATATGAAAATTAGCCAGGCATGATGGCACATGCTGGT A G NOM1 Ensembl:ENSG00000146909 Protein coding 3'UTR GSE100210;GSE99789 HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 29129909,29796672 RNA-Seq:(High) rs1439039685 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106494,RMVar_hsa_circ_249760,RMVar_hsa_circ_84383,RMVar_hsa_circ_249767 25327 RMVar_ID_25327 Human_SNP_ID_346775499 A-to-I Human chr7 + 156972691 156972691 156972691 GTCTCTATGAAAAATATAAAAATTAGCTGGGCATGGTGGCAGGCACCTGTAATCCCAGCTACTCG GTCTCTATGAAAAATATAAAAATTAGCTGGGCGTGGTGGCAGGCACCTGTAATCCCAGCTACTCG A G NOM1 Ensembl:ENSG00000146909 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs546854373 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106494,RMVar_hsa_circ_249760,RMVar_hsa_circ_84383,RMVar_hsa_circ_249767 25328 RMVar_ID_25328 Human_SNP_ID_346776465 A-to-I Human chr7 + 156975970 156975970 156975970 CAGGCTGGAGTATAACGGCGCAATTTGGGCTCACTGCAACCTCCATCTCCCTGGTTCAAGTGATT CAGGCTGGAGTATAACGGCGCAATTTGGGCTCGCTGCAACCTCCATCTCCCTGGTTCAAGTGATT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs981709621 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7717452,Human_RBP_ID_16090860 25329 RMVar_ID_25329 Human_SNP_ID_346825902 A-to-I Human chr7 + 157156541 157156541 157156541 GTTGGCTGGGCTGGTCTTGAACTCCTAACCTCAAGTGATCCACTACCCTGGCCTCCAAAACTGCT GTTGGCTGGGCTGGTCTTGAACTCCTAACCTCGAGTGATCCACTACCCTGGCCTCCAAAACTGCT A G UBE3C Ensembl:ENSG00000009335 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs969536655 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26088859 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 25330 RMVar_ID_25330 Human_SNP_ID_346828660 A-to-I Human chr7 + 157166619 157166619 157166619 AAAATTACCCAGGCATGCTGGCGCATGCCTGTAATCCCAGCTCCTCGGGAGCCTGAGGCAGGAGA AAAATTACCCAGGCATGCTGGCGCATGCCTGTCATCCCAGCTCCTCGGGAGCCTGAGGCAGGAGA A C UBE3C Ensembl:ENSG00000009335 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs920495136 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_249776,RMVar_hsa_circ_101933,RMVar_hsa_circ_126971,RMVar_hsa_circ_123177,RMVar_hsa_circ_272647,RMVar_hsa_circ_249768,RMVar_hsa_circ_249770,RMVar_hsa_circ_84720,RMVar_hsa_circ_249771,RMVar_hsa_circ_249769,RMVar_hsa_circ_319946,RMVar_hsa_circ_335159,RMVar_hsa_circ_345337,RMVar_hsa_circ_361270,RMVar_hsa_circ_355800,RMVar_hsa_circ_327051,RMVar_hsa_circ_287621,RMVar_hsa_circ_293199,RMVar_hsa_circ_284740,RMVar_hsa_circ_249780,RMVar_hsa_circ_49063,RMVar_hsa_circ_125127,RMVar_hsa_circ_20640,RMVar_hsa_circ_249781,RMVar_hsa_circ_249778,RMVar_hsa_circ_249779,RMVar_hsa_circ_249777,RMVar_hsa_circ_8783,RMVar_hsa_circ_249774,RMVar_hsa_circ_249775,RMVar_hsa_circ_249773 25331 RMVar_ID_25331 Human_SNP_ID_346842271 A-to-I Human chr7 + 157218182 157218182 157218182 AAAGAAACCATGTCGGCTGGGCGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAG AAAGAAACCATGTCGGCTGGGCGCGGTGGCTCTTGCCTGTAATCCCAGCACTTTGGGAGGCCAAG A T UBE3C Ensembl:ENSG00000009335 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1008728671 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16095036 RMVar_hsa_circ_126971,RMVar_hsa_circ_123177,RMVar_hsa_circ_249768,RMVar_hsa_circ_249769,RMVar_hsa_circ_361270,RMVar_hsa_circ_355800,RMVar_hsa_circ_249780,RMVar_hsa_circ_49063,RMVar_hsa_circ_249781,RMVar_hsa_circ_320562,RMVar_hsa_circ_338265,RMVar_hsa_circ_300471,RMVar_hsa_circ_278566,RMVar_hsa_circ_26678,RMVar_hsa_circ_249783,RMVar_hsa_circ_249782,RMVar_hsa_circ_50243,RMVar_hsa_circ_26805,RMVar_hsa_circ_20493,RMVar_hsa_circ_105488,RMVar_hsa_circ_249792,RMVar_hsa_circ_89058,RMVar_hsa_circ_249793,RMVar_hsa_circ_325837,RMVar_hsa_circ_108888,RMVar_hsa_circ_249796,RMVar_hsa_circ_249795,RMVar_hsa_circ_374912,RMVar_hsa_circ_249804,RMVar_hsa_circ_303297,RMVar_hsa_circ_353404,RMVar_hsa_circ_284174,RMVar_hsa_circ_118739,RMVar_hsa_circ_272453,RMVar_hsa_circ_59731,RMVar_hsa_circ_249805,RMVar_hsa_circ_249807,RMVar_hsa_circ_249808,RMVar_hsa_circ_249806,RMVar_hsa_circ_249814,RMVar_hsa_circ_284164,RMVar_hsa_circ_337456,RMVar_hsa_circ_344286,RMVar_hsa_circ_285680,RMVar_hsa_circ_104792,RMVar_hsa_circ_249812,RMVar_hsa_circ_249813,RMVar_hsa_circ_249811,RMVar_hsa_circ_249818,RMVar_hsa_circ_287717,RMVar_hsa_circ_339355,RMVar_hsa_circ_340979,RMVar_hsa_circ_323490,RMVar_hsa_circ_49121,RMVar_hsa_circ_249819 25332 RMVar_ID_25332 Human_SNP_ID_346845367 A-to-I Human chr7 + 157229822 157229822 157229822 TTTGTAGAGACAGGGTCTTGCTAGTGTTGCCCAGGCTGGTCTTGGACTCCTGGCCTCAGGCAGTC TTTGTAGAGACAGGGTCTTGCTAGTGTTGCCCGGGCTGGTCTTGGACTCCTGGCCTCAGGCAGTC A G UBE3C Ensembl:ENSG00000009335 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1211469860 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16095479 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 25333 RMVar_ID_25333 Human_SNP_ID_346846112 A-to-I Human chr7 + 157232458 157232458 157232458 TCTGCTCACTGCAAACTCCACCTCTCAGGTTCAAGGGATTGTCCTGCATCAGCCTCCTGAACAAC TCTGCTCACTGCAAACTCCACCTCTCAGGTTCGAGGGATTGTCCTGCATCAGCCTCCTGAACAAC A G UBE3C Ensembl:ENSG00000009335 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1334032096 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3075793,Human_RBP_ID_8663131,Human_RBP_ID_16095609,Human_RBP_ID_17577650,Human_RBP_ID_18879427,Human_RBP_ID_22622170 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 25334 RMVar_ID_25334 Human_SNP_ID_346846242 A-to-I Human chr7 + 157232969 157232969 157232969 AGTTCAGTGGTTTTTAATATATTCACTGTGTTATGTGACCATCACCAATATCAAACTTGGAAGCA AGTTCAGTGGTTTTTAATATATTCACTGTGTTGTGTGACCATCACCAATATCAAACTTGGAAGCA A G UBE3C Ensembl:ENSG00000009335 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs991066678 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3075804,Human_RBP_ID_3839294,Human_RBP_ID_21470075 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 25335 RMVar_ID_25335 Human_SNP_ID_346846243 A-to-I Human chr7 + 157232969 157232969 157232969 AGTTCAGTGGTTTTTAATATATTCACTGTGTTATGTGACCATCACCAATATCAAACTTGGAAGCA AGTTCAGTGGTTTTTAATATATTCACTGTGTTTTGTGACCATCACCAATATCAAACTTGGAAGCA A T UBE3C Ensembl:ENSG00000009335 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs991066678 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3075804,Human_RBP_ID_3839294,Human_RBP_ID_21470075 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 25336 RMVar_ID_25336 Human_SNP_ID_346852008 A-to-I Human chr7 + 157254497 157254497 157254497 CCAGCTCACTGAAACCTTTGCCTCCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCGAATAGC CCAGCTCACTGAAACCTTTGCCTCCCGGGTTCGAGCAATTCTCCTGCCTCAGCCTCCCGAATAGC A G UBE3C Ensembl:ENSG00000009335 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs760834841 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49063,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_118739,RMVar_hsa_circ_249805,RMVar_hsa_circ_344286,RMVar_hsa_circ_339355,RMVar_hsa_circ_282679,RMVar_hsa_circ_249824,RMVar_hsa_circ_48156,RMVar_hsa_circ_103582,RMVar_hsa_circ_341147,RMVar_hsa_circ_249829,RMVar_hsa_circ_249832,RMVar_hsa_circ_327399 25337 RMVar_ID_25337 Human_SNP_ID_346852097 A-to-I Human chr7 + 157254820 157254820 157254820 CCCAGCCTTTGGGAGGCCGGGGCAGGTGGATCACTTGAGCTCAGGAGTTTGAAACCAGCCTGGGC CCCAGCCTTTGGGAGGCCGGGGCAGGTGGATCGCTTGAGCTCAGGAGTTTGAAACCAGCCTGGGC A G UBE3C Ensembl:ENSG00000009335 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs974681103 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49063,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_118739,RMVar_hsa_circ_249805,RMVar_hsa_circ_344286,RMVar_hsa_circ_339355,RMVar_hsa_circ_282679,RMVar_hsa_circ_249824,RMVar_hsa_circ_48156,RMVar_hsa_circ_103582,RMVar_hsa_circ_341147,RMVar_hsa_circ_249829,RMVar_hsa_circ_249832,RMVar_hsa_circ_327399 25338 RMVar_ID_25338 Human_SNP_ID_346852098 A-to-I Human chr7 + 157254820 157254820 157254820 CCCAGCCTTTGGGAGGCCGGGGCAGGTGGATCACTTGAGCTCAGGAGTTTGAAACCAGCCTGGGC CCCAGCCTTTGGGAGGCCGGGGCAGGTGGATCTCTTGAGCTCAGGAGTTTGAAACCAGCCTGGGC A T UBE3C Ensembl:ENSG00000009335 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs974681103 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49063,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_118739,RMVar_hsa_circ_249805,RMVar_hsa_circ_344286,RMVar_hsa_circ_339355,RMVar_hsa_circ_282679,RMVar_hsa_circ_249824,RMVar_hsa_circ_48156,RMVar_hsa_circ_103582,RMVar_hsa_circ_341147,RMVar_hsa_circ_249829,RMVar_hsa_circ_249832,RMVar_hsa_circ_327399 25339 RMVar_ID_25339 Human_SNP_ID_346853090 A-to-I Human chr7 + 157258515 157258515 157258515 TACTCTGTCGCCCAGGCTGGAGTGCAGAGGGCAATGGCGTGATTTCCGCTCACTGCAACCTCTGC TACTCTGTCGCCCAGGCTGGAGTGCAGAGGGCTATGGCGTGATTTCCGCTCACTGCAACCTCTGC A T UBE3C Ensembl:ENSG00000009335 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs367947975 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105488,RMVar_hsa_circ_249792,RMVar_hsa_circ_108888,RMVar_hsa_circ_249795,RMVar_hsa_circ_118739,RMVar_hsa_circ_249805,RMVar_hsa_circ_103582,RMVar_hsa_circ_249829 25340 RMVar_ID_25340 Human_SNP_ID_346854546 A-to-I Human chr7 + 157263543 157263543 157263543 AAAATTAGCTAGGTGTGATGATGGGCACATATAGTCCCAGCTACTCGGGAGGTTGAGGCAAGAGA AAAATTAGCTAGGTGTGATGATGGGCACATATGGTCCCAGCTACTCGGGAGGTTGAGGCAAGAGA A G UBE3C Ensembl:ENSG00000009335 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs892096601 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16096823 RMVar_hsa_circ_105488,RMVar_hsa_circ_249792,RMVar_hsa_circ_108888,RMVar_hsa_circ_249795,RMVar_hsa_circ_118739,RMVar_hsa_circ_249805,RMVar_hsa_circ_103582,RMVar_hsa_circ_249829 25341 RMVar_ID_25341 Human_SNP_ID_346854987 A-to-I Human chr7 + 157264751 157264751 157264751 GCACCACTACAGCCGGCTAATTTTTTATTTTTAGTAGAGATGGGGTTTCGCCATGTTGGTCAGGC GCACCACTACAGCCGGCTAATTTTTTATTTTTGGTAGAGATGGGGTTTCGCCATGTTGGTCAGGC A G UBE3C Ensembl:ENSG00000009335 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1563081063 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105488,RMVar_hsa_circ_249792,RMVar_hsa_circ_108888,RMVar_hsa_circ_249795,RMVar_hsa_circ_118739,RMVar_hsa_circ_249805,RMVar_hsa_circ_103582,RMVar_hsa_circ_249829 25342 RMVar_ID_25342 Human_SNP_ID_346855004 A-to-I Human chr7 + 157264806 157264806 157264806 TTGGTCAGGCTGGTCTCAGAAATCCTGACCTCAGGTGATCCACCCGTTGTGGCCTCCCAAAATGC TTGGTCAGGCTGGTCTCAGAAATCCTGACCTCTGGTGATCCACCCGTTGTGGCCTCCCAAAATGC A T UBE3C Ensembl:ENSG00000009335 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs994560972 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26089878 RMVar_hsa_circ_105488,RMVar_hsa_circ_249792,RMVar_hsa_circ_108888,RMVar_hsa_circ_249795,RMVar_hsa_circ_118739,RMVar_hsa_circ_249805,RMVar_hsa_circ_103582,RMVar_hsa_circ_249829 25343 RMVar_ID_25343 Human_SNP_ID_346855687 A-to-I Human chr7 + 157267354 157267353 157267354 TGAGGCAGGAGAATCGCTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCTGAGATGGCGCCATTGC TGAGGCAGGAGAATCGCTTGAACCTGGGAGGC_GAGGTTGCAGTGAGCTGAGATGGCGCCATTGC CA C UBE3C Ensembl:ENSG00000009335 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs559507462 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_105488,RMVar_hsa_circ_249792,RMVar_hsa_circ_108888,RMVar_hsa_circ_249795,RMVar_hsa_circ_118739,RMVar_hsa_circ_249805,RMVar_hsa_circ_103582,RMVar_hsa_circ_249829 25344 RMVar_ID_25344 Human_SNP_ID_347018423 A-to-I Human chr7 - 157800788 157800788 157800788 GCCACCACACCCGGCTGGTTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCGTGTTGGCCAGGA GCCACCACACCCGGCTGGTTTTTTGTATTTTTGGTAGAGACGGGGTTTCACCGTGTTGGCCAGGA T C PTPRN2 Ensembl:ENSG00000155093 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs536962389 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_177358 RMVar_hsa_circ_49649 25345 RMVar_ID_25345 Human_SNP_ID_347273769 A-to-I Human chr7 - 158628549 158628549 158628549 GGAGTGCAATGGTGCGATCTTGGCTCACTGCAACCTCTGCCTCCTGGGTTCATGCAGTCCTCCTG GGAGTGCAATGGTGCGATCTTGGCTCACTGCATCCTCTGCCTCCTGGGTTCATGCAGTCCTCCTG T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs553751886 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16101208 25346 RMVar_ID_25346 Human_SNP_ID_347273770 A-to-I Human chr7 - 158628549 158628549 158628549 GGAGTGCAATGGTGCGATCTTGGCTCACTGCAACCTCTGCCTCCTGGGTTCATGCAGTCCTCCTG GGAGTGCAATGGTGCGATCTTGGCTCACTGCAGCCTCTGCCTCCTGGGTTCATGCAGTCCTCCTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs553751886 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16101208 25347 RMVar_ID_25347 Human_SNP_ID_347276186 A-to-I Human chr7 - 158638106 158638106 158638106 AGAGTCTCCCTCTGTTATGCAGGCTGTAGTGCAGTGGTGCGATCTTGGCTCACTGCAACCTTTGC AGAGTCTCCCTCTGTTATGCAGGCTGTAGTGCGGTGGTGCGATCTTGGCTCACTGCAACCTTTGC T C NCAPG2 Ensembl:ENSG00000146918 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs920512669 Functional Loss SNV dbSNP153 33..33 33 - - - 25348 RMVar_ID_25348 Human_SNP_ID_347276732 A-to-I Human chr7 - 158640481 158640481 158640481 TTGCCTAGGGTGGAACGCAGTGGTGTGATCTCAGTTCACTGCAACCTCTGCCTCCTAAGTTCAAA TTGCCTAGGGTGGAACGCAGTGGTGTGATCTCGGTTCACTGCAACCTCTGCCTCCTAAGTTCAAA T C NCAPG2 Ensembl:ENSG00000146918 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947223928 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3076813,Human_RBP_ID_7719459,Human_RBP_ID_8663474,Human_RBP_ID_16101744,Human_RBP_ID_21471327,Human_RBP_ID_24439324,Human_RBP_ID_26090442 25349 RMVar_ID_25349 Human_SNP_ID_347278148 A-to-I Human chr7 - 158646810 158646810 158646810 TTGACTAGCCTGATCTTGAACTCCTGACCTCAAGCATTCCTCTTGCCTCAGCCTCCCAGAGCGCT TTGACTAGCCTGATCTTGAACTCCTGACCTCAGGCATTCCTCTTGCCTCAGCCTCCCAGAGCGCT T C NCAPG2 Ensembl:ENSG00000146918 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042683913 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16102031,Human_RBP_ID_23315294 RMVar_hsa_circ_15294,RMVar_hsa_circ_363090,RMVar_hsa_circ_266499,RMVar_hsa_circ_44938 25350 RMVar_ID_25350 Human_SNP_ID_347278167 A-to-I Human chr7 - 158646905 158646905 158646905 CCTGCCTCAGTCTCCCAAGTAGCTGGGACTACAGGTATGCACCACCATGCCCAGCTAATTTTAAA CCTGCCTCAGTCTCCCAAGTAGCTGGGACTACGGGTATGCACCACCATGCCCAGCTAATTTTAAA T C NCAPG2 Ensembl:ENSG00000146918 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1436887038 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15294,RMVar_hsa_circ_363090,RMVar_hsa_circ_266499,RMVar_hsa_circ_44938 25351 RMVar_ID_25351 Human_SNP_ID_347288154 A-to-I Human chr7 - 158680004 158680004 158680004 CATTTCCTATTAGGGATCCAAACCTTCATGCTATTGAAATGGATAGTGAAATCCAGAAACAGTTT CATTTCCTATTAGGGATCCAAACCTTCATGCTGTTGAAATGGATAGTGAAATCCAGAAACAGTTT T C NCAPG2 Ensembl:ENSG00000146918 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs749084114 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2039095,Human_RBP_ID_4934081,Human_RBP_ID_19139533 Human_Splice_Rec_943336,Human_Splice_Rec_943337,Human_Splice_Rec_943392,Human_Splice_Rec_943393,Human_Splice_Rec_943450,Human_Splice_Rec_943451,Human_Splice_Rec_943494,Human_Splice_Rec_943495,Human_Splice_Rec_943542,Human_Splice_Rec_943543,Human_Splice_Rec_943594,Human_Splice_Rec_943595 RMVar_hsa_circ_14230,RMVar_hsa_circ_266499,RMVar_hsa_circ_8241,RMVar_hsa_circ_249877,RMVar_hsa_circ_317489,RMVar_hsa_circ_351477,RMVar_hsa_circ_371940,RMVar_hsa_circ_334746,RMVar_hsa_circ_40954,RMVar_hsa_circ_377330,RMVar_hsa_circ_249876,RMVar_hsa_circ_304072,RMVar_hsa_circ_33328,RMVar_hsa_circ_249878 25352 RMVar_ID_25352 Human_SNP_ID_347305320 A-to-I Human chr7 - 158738164 158738164 158738164 GGGATTACAGGCGTGCACTACCTCGTCCGACTAACTTGTATTTTTAGTAGACACGGGGTTTCACC GGGATTACAGGCGTGCACTACCTCGTCCGACTTACTTGTATTTTTAGTAGACACGGGGTTTCACC T A ESYT2 Ensembl:ENSG00000117868 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1343531995 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_249881,RMVar_hsa_circ_104946,RMVar_hsa_circ_114222,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_21699,RMVar_hsa_circ_102537,RMVar_hsa_circ_249880,RMVar_hsa_circ_266906,RMVar_hsa_circ_268736,RMVar_hsa_circ_288367,RMVar_hsa_circ_310916,RMVar_hsa_circ_249885,RMVar_hsa_circ_325077,RMVar_hsa_circ_299803,RMVar_hsa_circ_278055,RMVar_hsa_circ_84320,RMVar_hsa_circ_249887,RMVar_hsa_circ_249888,RMVar_hsa_circ_249886,RMVar_hsa_circ_249889 25353 RMVar_ID_25353 Human_SNP_ID_347305330 A-to-I Human chr7 - 158738203 158738203 158738203 GGTTCAAGCAATTCTCCTGCCTCAGCCACCCGAGTAGGTGGGATTACAGGCGTGCACTACCTCGT GGTTCAAGCAATTCTCCTGCCTCAGCCACCCGCGTAGGTGGGATTACAGGCGTGCACTACCTCGT T G ESYT2 Ensembl:ENSG00000117868 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1401473403 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24204699,Human_RBP_ID_26551864 RMVar_hsa_circ_249881,RMVar_hsa_circ_104946,RMVar_hsa_circ_114222,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_21699,RMVar_hsa_circ_102537,RMVar_hsa_circ_249880,RMVar_hsa_circ_266906,RMVar_hsa_circ_268736,RMVar_hsa_circ_288367,RMVar_hsa_circ_310916,RMVar_hsa_circ_249885,RMVar_hsa_circ_325077,RMVar_hsa_circ_299803,RMVar_hsa_circ_278055,RMVar_hsa_circ_84320,RMVar_hsa_circ_249887,RMVar_hsa_circ_249888,RMVar_hsa_circ_249886,RMVar_hsa_circ_249889 25354 RMVar_ID_25354 Human_SNP_ID_347305552 A-to-I Human chr7 - 158738557 158738557 158738557 CCAGCTACTAGGGAGGCTGATGCAGGAGAATCACTTGAACCCAGGAGGCAGAGGTTGCTGTGAGC CCAGCTACTAGGGAGGCTGATGCAGGAGAATCGCTTGAACCCAGGAGGCAGAGGTTGCTGTGAGC T C ESYT2 Ensembl:ENSG00000117868 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1419000460 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_249881,RMVar_hsa_circ_104946,RMVar_hsa_circ_114222,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_21699,RMVar_hsa_circ_102537,RMVar_hsa_circ_249880,RMVar_hsa_circ_266906,RMVar_hsa_circ_268736,RMVar_hsa_circ_288367,RMVar_hsa_circ_310916,RMVar_hsa_circ_249885,RMVar_hsa_circ_325077,RMVar_hsa_circ_299803,RMVar_hsa_circ_278055,RMVar_hsa_circ_84320,RMVar_hsa_circ_249887,RMVar_hsa_circ_249888,RMVar_hsa_circ_249886,RMVar_hsa_circ_249889 25355 RMVar_ID_25355 Human_SNP_ID_347314838 A-to-I Human chr7 - 158771936 158771936 158771936 TTGTATTTTTTTAGTAGAGATGGGGTTTCGCCATGTTGGCCAGGCTGGTCTTGAACTCCTGAGCT TTGTATTTTTTTAGTAGAGATGGGGTTTCGCCTTGTTGGCCAGGCTGGTCTTGAACTCCTGAGCT T A ESYT2 Ensembl:ENSG00000117868 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1210374672 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71961,RMVar_hsa_circ_249897,RMVar_hsa_circ_17956,RMVar_hsa_circ_20079,RMVar_hsa_circ_249895,RMVar_hsa_circ_78023,RMVar_hsa_circ_249898,RMVar_hsa_circ_321197,RMVar_hsa_circ_18758,RMVar_hsa_circ_58065,RMVar_hsa_circ_249899,RMVar_hsa_circ_299221,RMVar_hsa_circ_71554,RMVar_hsa_circ_37909,RMVar_hsa_circ_249906,RMVar_hsa_circ_354281,RMVar_hsa_circ_285241,RMVar_hsa_circ_273871,RMVar_hsa_circ_276962,RMVar_hsa_circ_126642,RMVar_hsa_circ_249910,RMVar_hsa_circ_249912,RMVar_hsa_circ_249913,RMVar_hsa_circ_249914,RMVar_hsa_circ_249911,RMVar_hsa_circ_371194,RMVar_hsa_circ_27341,RMVar_hsa_circ_35599,RMVar_hsa_circ_54523,RMVar_hsa_circ_249915,RMVar_hsa_circ_295299,RMVar_hsa_circ_363232,RMVar_hsa_circ_249920,RMVar_hsa_circ_249919,RMVar_hsa_circ_368112,RMVar_hsa_circ_371784,RMVar_hsa_circ_378869,RMVar_hsa_circ_267553 25356 RMVar_ID_25356 Human_SNP_ID_347314839 A-to-I Human chr7 - 158771936 158771936 158771936 TTGTATTTTTTTAGTAGAGATGGGGTTTCGCCATGTTGGCCAGGCTGGTCTTGAACTCCTGAGCT TTGTATTTTTTTAGTAGAGATGGGGTTTCGCCGTGTTGGCCAGGCTGGTCTTGAACTCCTGAGCT T C ESYT2 Ensembl:ENSG00000117868 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1210374672 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71961,RMVar_hsa_circ_249897,RMVar_hsa_circ_17956,RMVar_hsa_circ_20079,RMVar_hsa_circ_249895,RMVar_hsa_circ_78023,RMVar_hsa_circ_249898,RMVar_hsa_circ_321197,RMVar_hsa_circ_18758,RMVar_hsa_circ_58065,RMVar_hsa_circ_249899,RMVar_hsa_circ_299221,RMVar_hsa_circ_71554,RMVar_hsa_circ_37909,RMVar_hsa_circ_249906,RMVar_hsa_circ_354281,RMVar_hsa_circ_285241,RMVar_hsa_circ_273871,RMVar_hsa_circ_276962,RMVar_hsa_circ_126642,RMVar_hsa_circ_249910,RMVar_hsa_circ_249912,RMVar_hsa_circ_249913,RMVar_hsa_circ_249914,RMVar_hsa_circ_249911,RMVar_hsa_circ_371194,RMVar_hsa_circ_27341,RMVar_hsa_circ_35599,RMVar_hsa_circ_54523,RMVar_hsa_circ_249915,RMVar_hsa_circ_295299,RMVar_hsa_circ_363232,RMVar_hsa_circ_249920,RMVar_hsa_circ_249919,RMVar_hsa_circ_368112,RMVar_hsa_circ_371784,RMVar_hsa_circ_378869,RMVar_hsa_circ_267553 25357 RMVar_ID_25357 Human_SNP_ID_347314870 A-to-I Human chr7 - 158772040 158772040 158772040 TCAGCTCACTGCAAGCACCACCTCCCAGGTTCAAGCAATTCTCCCTGCCTCAGCCTCCCAAGTAG TCAGCTCACTGCAAGCACCACCTCCCAGGTTCGAGCAATTCTCCCTGCCTCAGCCTCCCAAGTAG T C ESYT2 Ensembl:ENSG00000117868 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1183217410 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71961,RMVar_hsa_circ_249897,RMVar_hsa_circ_17956,RMVar_hsa_circ_20079,RMVar_hsa_circ_249895,RMVar_hsa_circ_78023,RMVar_hsa_circ_249898,RMVar_hsa_circ_321197,RMVar_hsa_circ_18758,RMVar_hsa_circ_58065,RMVar_hsa_circ_249899,RMVar_hsa_circ_299221,RMVar_hsa_circ_71554,RMVar_hsa_circ_37909,RMVar_hsa_circ_249906,RMVar_hsa_circ_354281,RMVar_hsa_circ_285241,RMVar_hsa_circ_273871,RMVar_hsa_circ_276962,RMVar_hsa_circ_126642,RMVar_hsa_circ_249910,RMVar_hsa_circ_249912,RMVar_hsa_circ_249913,RMVar_hsa_circ_249914,RMVar_hsa_circ_249911,RMVar_hsa_circ_371194,RMVar_hsa_circ_27341,RMVar_hsa_circ_35599,RMVar_hsa_circ_54523,RMVar_hsa_circ_249915,RMVar_hsa_circ_295299,RMVar_hsa_circ_363232,RMVar_hsa_circ_249920,RMVar_hsa_circ_249919,RMVar_hsa_circ_368112,RMVar_hsa_circ_371784,RMVar_hsa_circ_378869,RMVar_hsa_circ_267553 25358 RMVar_ID_25358 Human_SNP_ID_347314884 A-to-I Human chr7 - 158772120 158772120 158772120 GGTAAATAAGTAAGTTTCTTTTTTTTTTTTTGAGATGGAATCTCACTCTGTTGCCCAGGCTGGAG GGTAAATAAGTAAGTTTCTTTTTTTTTTTTTGTGATGGAATCTCACTCTGTTGCCCAGGCTGGAG T A ESYT2 Ensembl:ENSG00000117868 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1233616712 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71961,RMVar_hsa_circ_249897,RMVar_hsa_circ_17956,RMVar_hsa_circ_20079,RMVar_hsa_circ_249895,RMVar_hsa_circ_78023,RMVar_hsa_circ_249898,RMVar_hsa_circ_321197,RMVar_hsa_circ_18758,RMVar_hsa_circ_58065,RMVar_hsa_circ_249899,RMVar_hsa_circ_299221,RMVar_hsa_circ_71554,RMVar_hsa_circ_37909,RMVar_hsa_circ_249906,RMVar_hsa_circ_354281,RMVar_hsa_circ_285241,RMVar_hsa_circ_273871,RMVar_hsa_circ_276962,RMVar_hsa_circ_126642,RMVar_hsa_circ_249910,RMVar_hsa_circ_249912,RMVar_hsa_circ_249913,RMVar_hsa_circ_249914,RMVar_hsa_circ_249911,RMVar_hsa_circ_371194,RMVar_hsa_circ_27341,RMVar_hsa_circ_35599,RMVar_hsa_circ_54523,RMVar_hsa_circ_249915,RMVar_hsa_circ_295299,RMVar_hsa_circ_363232,RMVar_hsa_circ_249920,RMVar_hsa_circ_249919,RMVar_hsa_circ_368112,RMVar_hsa_circ_371784,RMVar_hsa_circ_378869,RMVar_hsa_circ_267553 25359 RMVar_ID_25359 Human_SNP_ID_347320582 A-to-I Human chr7 - 158791293 158791293 158791293 CGATGAATGGATAAGCAGAATGTGGCCTGTACACCTTAGAAACACGGGACTCCTGCTCCAGGCCG CGATGAATGGATAAGCAGAATGTGGCCTGTACGCCTTAGAAACACGGGACTCCTGCTCCAGGCCG T C ESYT2 Ensembl:ENSG00000117868 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs844522 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2425,GWAS_ID_2426,GWAS_ID_2427,GWAS_ID_2428,GWAS_ID_2429,GWAS_ID_2430,GWAS_ID_2431,GWAS_ID_2432,GWAS_ID_2433 RMVar_hsa_circ_249897,RMVar_hsa_circ_17956,RMVar_hsa_circ_20079,RMVar_hsa_circ_249895,RMVar_hsa_circ_78023,RMVar_hsa_circ_249898,RMVar_hsa_circ_58065,RMVar_hsa_circ_249899,RMVar_hsa_circ_299221,RMVar_hsa_circ_71554,RMVar_hsa_circ_249906,RMVar_hsa_circ_354281,RMVar_hsa_circ_273871,RMVar_hsa_circ_249913,RMVar_hsa_circ_249914,RMVar_hsa_circ_371194,RMVar_hsa_circ_249921,RMVar_hsa_circ_27341,RMVar_hsa_circ_54523,RMVar_hsa_circ_249915,RMVar_hsa_circ_295299,RMVar_hsa_circ_249920,RMVar_hsa_circ_249919,RMVar_hsa_circ_368112,RMVar_hsa_circ_371784,RMVar_hsa_circ_378869,RMVar_hsa_circ_249923,RMVar_hsa_circ_291852,RMVar_hsa_circ_326599,RMVar_hsa_circ_282781,RMVar_hsa_circ_249922,RMVar_hsa_circ_249925,RMVar_hsa_circ_249927,RMVar_hsa_circ_284055,RMVar_hsa_circ_311640,RMVar_hsa_circ_310687,RMVar_hsa_circ_249926,RMVar_hsa_circ_267630 25360 RMVar_ID_25360 Human_SNP_ID_347321229 A-to-I Human chr7 - 158793447 158793447 158793447 CTAACAGCCTTGATCATTGCCATTCATAAAATATGTTAAATAAGAAGTTAAAGACACTGCAAAAA CTAACAGCCTTGATCATTGCCATTCATAAAATTTGTTAAATAAGAAGTTAAAGACACTGCAAAAA T A ESYT2 Ensembl:ENSG00000117868 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2602552 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2434,GWAS_ID_2435,GWAS_ID_2436,GWAS_ID_2437,GWAS_ID_2438,GWAS_ID_2439,GWAS_ID_2440,GWAS_ID_2441,GWAS_ID_2442 RMVar_hsa_circ_249897,RMVar_hsa_circ_17956,RMVar_hsa_circ_20079,RMVar_hsa_circ_249895,RMVar_hsa_circ_78023,RMVar_hsa_circ_249898,RMVar_hsa_circ_58065,RMVar_hsa_circ_249899,RMVar_hsa_circ_299221,RMVar_hsa_circ_71554,RMVar_hsa_circ_249906,RMVar_hsa_circ_354281,RMVar_hsa_circ_273871,RMVar_hsa_circ_249913,RMVar_hsa_circ_249914,RMVar_hsa_circ_371194,RMVar_hsa_circ_249921,RMVar_hsa_circ_27341,RMVar_hsa_circ_54523,RMVar_hsa_circ_249915,RMVar_hsa_circ_295299,RMVar_hsa_circ_249920,RMVar_hsa_circ_249919,RMVar_hsa_circ_368112,RMVar_hsa_circ_371784,RMVar_hsa_circ_378869,RMVar_hsa_circ_249923,RMVar_hsa_circ_291852,RMVar_hsa_circ_326599,RMVar_hsa_circ_282781,RMVar_hsa_circ_249922,RMVar_hsa_circ_249925,RMVar_hsa_circ_249927,RMVar_hsa_circ_284055,RMVar_hsa_circ_311640,RMVar_hsa_circ_310687,RMVar_hsa_circ_249926,RMVar_hsa_circ_267630 25361 RMVar_ID_25361 Human_SNP_ID_347321230 A-to-I Human chr7 - 158793447 158793447 158793447 CTAACAGCCTTGATCATTGCCATTCATAAAATATGTTAAATAAGAAGTTAAAGACACTGCAAAAA CTAACAGCCTTGATCATTGCCATTCATAAAATGTGTTAAATAAGAAGTTAAAGACACTGCAAAAA T C ESYT2 Ensembl:ENSG00000117868 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2602552 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2434,GWAS_ID_2435,GWAS_ID_2436,GWAS_ID_2437,GWAS_ID_2438,GWAS_ID_2439,GWAS_ID_2440,GWAS_ID_2441,GWAS_ID_2442 RMVar_hsa_circ_249897,RMVar_hsa_circ_17956,RMVar_hsa_circ_20079,RMVar_hsa_circ_249895,RMVar_hsa_circ_78023,RMVar_hsa_circ_249898,RMVar_hsa_circ_58065,RMVar_hsa_circ_249899,RMVar_hsa_circ_299221,RMVar_hsa_circ_71554,RMVar_hsa_circ_249906,RMVar_hsa_circ_354281,RMVar_hsa_circ_273871,RMVar_hsa_circ_249913,RMVar_hsa_circ_249914,RMVar_hsa_circ_371194,RMVar_hsa_circ_249921,RMVar_hsa_circ_27341,RMVar_hsa_circ_54523,RMVar_hsa_circ_249915,RMVar_hsa_circ_295299,RMVar_hsa_circ_249920,RMVar_hsa_circ_249919,RMVar_hsa_circ_368112,RMVar_hsa_circ_371784,RMVar_hsa_circ_378869,RMVar_hsa_circ_249923,RMVar_hsa_circ_291852,RMVar_hsa_circ_326599,RMVar_hsa_circ_282781,RMVar_hsa_circ_249922,RMVar_hsa_circ_249925,RMVar_hsa_circ_249927,RMVar_hsa_circ_284055,RMVar_hsa_circ_311640,RMVar_hsa_circ_310687,RMVar_hsa_circ_249926,RMVar_hsa_circ_267630 25362 RMVar_ID_25362 Human_SNP_ID_347329569 A-to-I Human chr7 - 158823151 158823151 158823151 ATCTGGGACTACAGGCGCACACCGCCACATCCAGCTAATTTCTTTTGTATTATAGTGCAGACAGG ATCTGGGACTACAGGCGCACACCGCCACATCCCGCTAATTTCTTTTGTATTATAGTGCAGACAGG T G ESYT2 Ensembl:ENSG00000117868 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1466665212 Functional Loss SNV dbSNP153 33..33 33 - - - 25363 RMVar_ID_25363 Human_SNP_ID_347329579 A-to-I Human chr7 - 158823173 158823173 158823173 CTCCTGCCTCAGCCTCCCAAGTATCTGGGACTACAGGCGCACACCGCCACATCCAGCTAATTTCT CTCCTGCCTCAGCCTCCCAAGTATCTGGGACTGCAGGCGCACACCGCCACATCCAGCTAATTTCT T C ESYT2 Ensembl:ENSG00000117868 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1321193631 Functional Loss SNV dbSNP153 33..33 33 - - - 25364 RMVar_ID_25364 Human_SNP_ID_347346868 A-to-I Human chr7 + 158882815 158882815 158882815 GGAGAATTGCTTGAACCTGGGAGGAAGAGGTTACGGTGAACTGAGATCGTGCCACTGCACTCCAG GGAGAATTGCTTGAACCTGGGAGGAAGAGGTTGCGGTGAACTGAGATCGTGCCACTGCACTCCAG A G WDR60 Ensembl:ENSG00000126870 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1013264745 Functional Loss SNV dbSNP153 33..33 33 - - - 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_51711,RMVar_hsa_circ_123835,RMVar_hsa_circ_18294,RMVar_hsa_circ_324452,RMVar_hsa_circ_63693,RMVar_hsa_circ_307793,RMVar_hsa_circ_317658,RMVar_hsa_circ_359522,RMVar_hsa_circ_308395,RMVar_hsa_circ_265648,RMVar_hsa_circ_249934,RMVar_hsa_circ_249936,RMVar_hsa_circ_249937,RMVar_hsa_circ_249935 25365 RMVar_ID_25365 Human_SNP_ID_256085060 A-to-I Human chr5 + 150015352 150015352 150015352 ACTCTGTTGCCCATGTTAGAGTGCAGTGGCACAATCATGGCTCACTGCATCCTTGACTTCCTGGG ACTCTGTTGCCCATGTTAGAGTGCAGTGGCACGATCATGGCTCACTGCATCCTTGACTTCCTGGG A G HMGXB3 Ensembl:ENSG00000113716 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1007954938 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_235416,RMVar_hsa_circ_112136,RMVar_hsa_circ_235415,RMVar_hsa_circ_374344,RMVar_hsa_circ_284162,RMVar_hsa_circ_48952,RMVar_hsa_circ_235419,RMVar_hsa_circ_235417,RMVar_hsa_circ_365706,RMVar_hsa_circ_272213,RMVar_hsa_circ_275722,RMVar_hsa_circ_373951,RMVar_hsa_circ_293360,RMVar_hsa_circ_235420,RMVar_hsa_circ_117863,RMVar_hsa_circ_374724,RMVar_hsa_circ_65134,RMVar_hsa_circ_235422,RMVar_hsa_circ_235423 25366 RMVar_ID_25366 Human_SNP_ID_256085262 A-to-I Human chr5 + 150016220 150016220 150016220 CAAAAAATAGTTGGGTGTGGTGGTACACACCTATAGTCCCAGCTACTCAGGGCTGAGGTGGGAGG CAAAAAATAGTTGGGTGTGGTGGTACACACCTGTAGTCCCAGCTACTCAGGGCTGAGGTGGGAGG A G HMGXB3 Ensembl:ENSG00000113716 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs545065399 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_235416,RMVar_hsa_circ_112136,RMVar_hsa_circ_235415,RMVar_hsa_circ_374344,RMVar_hsa_circ_284162,RMVar_hsa_circ_48952,RMVar_hsa_circ_235419,RMVar_hsa_circ_235417,RMVar_hsa_circ_365706,RMVar_hsa_circ_272213,RMVar_hsa_circ_275722,RMVar_hsa_circ_373951,RMVar_hsa_circ_293360,RMVar_hsa_circ_235420,RMVar_hsa_circ_117863,RMVar_hsa_circ_374724,RMVar_hsa_circ_65134,RMVar_hsa_circ_235422,RMVar_hsa_circ_235423 25367 RMVar_ID_25367 Human_SNP_ID_256092579 A-to-I Human chr5 + 150047094 150047094 150047094 TTTTGTATTTTTAGAAGAGATGGGGTTTCACCATATTGGTCAGGCTGGTCTTGAACTTCTGACCT TTTTGTATTTTTAGAAGAGATGGGGTTTCACCGTATTGGTCAGGCTGGTCTTGAACTTCTGACCT A G HMGXB3 Ensembl:ENSG00000113716 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs896571647 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43730,RMVar_hsa_circ_330108,RMVar_hsa_circ_65193,RMVar_hsa_circ_87787,RMVar_hsa_circ_235431,RMVar_hsa_circ_73634 25368 RMVar_ID_25368 Human_SNP_ID_256092580 A-to-I Human chr5 + 150047096 150047096 150047096 TTGTATTTTTAGAAGAGATGGGGTTTCACCATATTGGTCAGGCTGGTCTTGAACTTCTGACCTCA TTGTATTTTTAGAAGAGATGGGGTTTCACCATGTTGGTCAGGCTGGTCTTGAACTTCTGACCTCA A G HMGXB3 Ensembl:ENSG00000113716 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1004420529 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43730,RMVar_hsa_circ_330108,RMVar_hsa_circ_65193,RMVar_hsa_circ_87787,RMVar_hsa_circ_235431,RMVar_hsa_circ_73634 25369 RMVar_ID_25369 Human_SNP_ID_256092581 A-to-I Human chr5 + 150047096 150047096 150047096 TTGTATTTTTAGAAGAGATGGGGTTTCACCATATTGGTCAGGCTGGTCTTGAACTTCTGACCTCA TTGTATTTTTAGAAGAGATGGGGTTTCACCATTTTGGTCAGGCTGGTCTTGAACTTCTGACCTCA A T HMGXB3 Ensembl:ENSG00000113716 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1004420529 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43730,RMVar_hsa_circ_330108,RMVar_hsa_circ_65193,RMVar_hsa_circ_87787,RMVar_hsa_circ_235431,RMVar_hsa_circ_73634 25370 RMVar_ID_25370 Human_SNP_ID_256092595 A-to-I Human chr5 + 150047186 150047186 150047186 AAAGTGCTAGGATTACAGGTGTGAGCCACTGCACCCGGCCCCCAGGGATTATTTTTTTAAGGTGC AAAGTGCTAGGATTACAGGTGTGAGCCACTGCCCCCGGCCCCCAGGGATTATTTTTTTAAGGTGC A C HMGXB3 Ensembl:ENSG00000113716 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs13189638 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43730,RMVar_hsa_circ_330108,RMVar_hsa_circ_65193,RMVar_hsa_circ_87787,RMVar_hsa_circ_235431,RMVar_hsa_circ_73634 25371 RMVar_ID_25371 Human_SNP_ID_256121455 A-to-I Human chr5 - 150152786 150152786 150152786 CTGAGAGAACCACTGCTCTCCTGGCCTCCTGCATTGGAACACTTGGCTGTGAAATTAATCTGCAA CTGAGAGAACCACTGCTCTCCTGGCCTCCTGCGTTGGAACACTTGGCTGTGAAATTAATCTGCAA T C PDGFRB Ensembl:ENSG00000113721 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs188825016 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77460,RMVar_hsa_circ_235440 25372 RMVar_ID_25372 Human_SNP_ID_256132436 A-to-I Human chr5 + 150196172 150196172 150196172 CAGCCCCAGGTTATGATAAAACACTTCCAACTAATTCTGCCCAAGGTCGCCTAGGAGGGGGTTGG CAGCCCCAGGTTATGATAAAACACTTCCAACTGATTCTGCCCAAGGTCGCCTAGGAGGGGGTTGG A G SLC6A7 Ensembl:ENSG00000011083 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1424811140 Functional Loss SNV dbSNP153 33..33 33 - - - 25373 RMVar_ID_25373 Human_SNP_ID_256141194 A-to-I Human chr5 - 150225946 150225946 150225946 GAGGTCAGGAGTTCAAGACCAGTCTGGCCAACATGGTGAAACGCCATCTTTACTAAAAATACAAA GAGGTCAGGAGTTCAAGACCAGTCTGGCCAACGTGGTGAAACGCCATCTTTACTAAAAATACAAA T C CAMK2A Ensembl:ENSG00000070808 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs893687712 Functional Loss SNV dbSNP153 33..33 33 - - - 25374 RMVar_ID_25374 Human_SNP_ID_256250446 A-to-I Human chr5 + 150655782 150655782 150655782 TCAAGCGATCCTCCTGCCTCAGCCCCCGCAGTAGCTGGGACTACAGGCACGCGCCACCGTGCCAC TCAAGCGATCCTCCTGCCTCAGCCCCCGCAGTGGCTGGGACTACAGGCACGCGCCACCGTGCCAC A G SYNPO Ensembl:ENSG00000171992 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs534576469 Functional Loss SNV dbSNP153 33..33 33 - - - 25375 RMVar_ID_25375 Human_SNP_ID_256262918 A-to-I Human chr5 - 150704200 150704200 150704200 TCCTAAATAAGATGGCTATAAGATGAAAAGCTACATGCCTCCCCCATATGTTGCCCAGTAATTCA TCCTAAATAAGATGGCTATAAGATGAAAAGCTTCATGCCTCCCCCATATGTTGCCCAGTAATTCA T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs752024355 Functional Loss SNV dbSNP153 33..33 33 - - - 25376 RMVar_ID_25376 Human_SNP_ID_256262919 A-to-I Human chr5 - 150704200 150704200 150704200 TCCTAAATAAGATGGCTATAAGATGAAAAGCTACATGCCTCCCCCATATGTTGCCCAGTAATTCA TCCTAAATAAGATGGCTATAAGATGAAAAGCTGCATGCCTCCCCCATATGTTGCCCAGTAATTCA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs752024355 Functional Loss SNV dbSNP153 33..33 33 - - - 25377 RMVar_ID_25377 Human_SNP_ID_256265199 A-to-I Human chr5 - 150713506 150713506 150713506 CCTAGGGGCGGGGGTTGCAGTGAACTCAGATCACGCCACTACACTCCAGCCTGGGCAACAGAGCC CCTAGGGGCGGGGGTTGCAGTGAACTCAGATCGCGCCACTACACTCCAGCCTGGGCAACAGAGCC T C DCTN4 Ensembl:ENSG00000132912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs986195601 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118724,RMVar_hsa_circ_125852,RMVar_hsa_circ_93780,RMVar_hsa_circ_105204,RMVar_hsa_circ_90060,RMVar_hsa_circ_235499,RMVar_hsa_circ_84557,RMVar_hsa_circ_88300,RMVar_hsa_circ_235501,RMVar_hsa_circ_235503,RMVar_hsa_circ_235504,RMVar_hsa_circ_235502,RMVar_hsa_circ_235500,RMVar_hsa_circ_235498 25378 RMVar_ID_25378 Human_SNP_ID_256265332 A-to-I Human chr5 - 150713988 150713988 150713988 CTCAGCCTCCTGAGGAGCTTGTATTACAGGCAAGCGCCACCACGCCTGGCCAATTTTTGTATTTT CTCAGCCTCCTGAGGAGCTTGTATTACAGGCAGGCGCCACCACGCCTGGCCAATTTTTGTATTTT T C DCTN4 Ensembl:ENSG00000132912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1244325455 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118724,RMVar_hsa_circ_125852,RMVar_hsa_circ_93780,RMVar_hsa_circ_105204,RMVar_hsa_circ_90060,RMVar_hsa_circ_235499,RMVar_hsa_circ_84557,RMVar_hsa_circ_88300,RMVar_hsa_circ_235501,RMVar_hsa_circ_235503,RMVar_hsa_circ_235504,RMVar_hsa_circ_235502,RMVar_hsa_circ_235500,RMVar_hsa_circ_235498 25379 RMVar_ID_25379 Human_SNP_ID_256265988 A-to-I Human chr5 - 150716750 150716750 150716750 CACGCCCGGCTAATTTTTTGCAGTTTTAGTAGAGACGGGGTTTCACCCTGTTGGCCAGGATGGTC CACGCCCGGCTAATTTTTTGCAGTTTTAGTAGCGACGGGGTTTCACCCTGTTGGCCAGGATGGTC T G DCTN4 Ensembl:ENSG00000132912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs549859374 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5068,RMVar_hsa_circ_125852,RMVar_hsa_circ_93780,RMVar_hsa_circ_105204,RMVar_hsa_circ_90060,RMVar_hsa_circ_235499,RMVar_hsa_circ_84557,RMVar_hsa_circ_88300,RMVar_hsa_circ_235501,RMVar_hsa_circ_235503,RMVar_hsa_circ_235504,RMVar_hsa_circ_235502,RMVar_hsa_circ_235500,RMVar_hsa_circ_265429,RMVar_hsa_circ_332009,RMVar_hsa_circ_375482,RMVar_hsa_circ_10608,RMVar_hsa_circ_235505 25380 RMVar_ID_25380 Human_SNP_ID_256265989 A-to-I Human chr5 - 150716752 150716752 150716752 ACCACGCCCGGCTAATTTTTTGCAGTTTTAGTAGAGACGGGGTTTCACCCTGTTGGCCAGGATGG ACCACGCCCGGCTAATTTTTTGCAGTTTTAGTGGAGACGGGGTTTCACCCTGTTGGCCAGGATGG T C DCTN4 Ensembl:ENSG00000132912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs921460905 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5068,RMVar_hsa_circ_125852,RMVar_hsa_circ_93780,RMVar_hsa_circ_105204,RMVar_hsa_circ_90060,RMVar_hsa_circ_235499,RMVar_hsa_circ_84557,RMVar_hsa_circ_88300,RMVar_hsa_circ_235501,RMVar_hsa_circ_235503,RMVar_hsa_circ_235504,RMVar_hsa_circ_235502,RMVar_hsa_circ_235500,RMVar_hsa_circ_265429,RMVar_hsa_circ_332009,RMVar_hsa_circ_375482,RMVar_hsa_circ_10608,RMVar_hsa_circ_235505 25381 RMVar_ID_25381 Human_SNP_ID_256269012 A-to-I Human chr5 - 150729098 150729098 150729098 TTGAGCCCAGGAGTTTGAGATCAGCCTAGGCAACATAGTGAGACCCTGTCTCTACCAAAAAAAAA TTGAGCCCAGGAGTTTGAGATCAGCCTAGGCAGCATAGTGAGACCCTGTCTCTACCAAAAAAAAA T C DCTN4 Ensembl:ENSG00000132912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1429554902 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5068,RMVar_hsa_circ_125852,RMVar_hsa_circ_93780,RMVar_hsa_circ_105204,RMVar_hsa_circ_90060,RMVar_hsa_circ_84557,RMVar_hsa_circ_235501,RMVar_hsa_circ_235503,RMVar_hsa_circ_235504,RMVar_hsa_circ_235502,RMVar_hsa_circ_235500,RMVar_hsa_circ_265429,RMVar_hsa_circ_375482,RMVar_hsa_circ_235506,RMVar_hsa_circ_368170,RMVar_hsa_circ_337404,RMVar_hsa_circ_235505,RMVar_hsa_circ_306974,RMVar_hsa_circ_367121,RMVar_hsa_circ_375547,RMVar_hsa_circ_271614,RMVar_hsa_circ_282251,RMVar_hsa_circ_235507 25382 RMVar_ID_25382 Human_SNP_ID_256270293 A-to-I Human chr5 - 150734027 150734026 150734027 CCACCATGCCCAGCTAATTTTTGCATTTTTTTATAGAGACAAGGTCTCACTCTGTTGTCCAGGCT CCACCATGCCCAGCTAATTTTTGCATTTTTTT_TAGAGACAAGGTCTCACTCTGTTGTCCAGGCT AT A DCTN4 Ensembl:ENSG00000132912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1426931197 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_15353563 RMVar_hsa_circ_125852,RMVar_hsa_circ_93780,RMVar_hsa_circ_90060,RMVar_hsa_circ_84557,RMVar_hsa_circ_235501,RMVar_hsa_circ_235503,RMVar_hsa_circ_235504,RMVar_hsa_circ_235502,RMVar_hsa_circ_265429,RMVar_hsa_circ_368170,RMVar_hsa_circ_375547,RMVar_hsa_circ_235507,RMVar_hsa_circ_312561,RMVar_hsa_circ_376508,RMVar_hsa_circ_366284 25383 RMVar_ID_25383 Human_SNP_ID_256341022 A-to-I Human chr5 - 151043572 151043572 151043572 TGGGGTTTTGCCATATTCTCCAGGCTGGTCTCAAACTCCTGAACTCAAGCAATTGGCCCACCTTG TGGGGTTTTGCCATATTCTCCAGGCTGGTCTCCAACTCCTGAACTCAAGCAATTGGCCCACCTTG T G TNIP1 Ensembl:ENSG00000145901 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1380624617 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15603,RMVar_hsa_circ_89626,RMVar_hsa_circ_235527 25384 RMVar_ID_25384 Human_SNP_ID_256341033 A-to-I Human chr5 - 151043618 151043618 151043618 GATGCGTGCCACCATGCCCGGCTAAATTTTGTATTTTTTGTAGAGATGGGGTTTTGCCATATTCT GATGCGTGCCACCATGCCCGGCTAAATTTTGTGTTTTTTGTAGAGATGGGGTTTTGCCATATTCT T C TNIP1 Ensembl:ENSG00000145901 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs140312148 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15603,RMVar_hsa_circ_89626,RMVar_hsa_circ_235527 25385 RMVar_ID_25385 Human_SNP_ID_256341179 A-to-I Human chr5 - 151044279 151044279 151044279 CCAGCACTTTGGGAGGCTGATGCAGGAAGATTACTTGCAACCAGGAGTTTGAGACCAGCCTGGGC CCAGCACTTTGGGAGGCTGATGCAGGAAGATTGCTTGCAACCAGGAGTTTGAGACCAGCCTGGGC T C TNIP1 Ensembl:ENSG00000145901 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1338687194 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15603,RMVar_hsa_circ_89626,RMVar_hsa_circ_235527 25386 RMVar_ID_25386 Human_SNP_ID_256341195 A-to-I Human chr5 - 151044321 151044321 151044321 AAAAATTAACTGGGTCAGGCGTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGATGC AAAAATTAACTGGGTCAGGCGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGATGC T C TNIP1 Ensembl:ENSG00000145901 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs538700563 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15603,RMVar_hsa_circ_89626,RMVar_hsa_circ_235527 25387 RMVar_ID_25387 Human_SNP_ID_256341438 A-to-I Human chr5 - 151045227 151045227 151045227 AAAATTAGCGGGCATGGTGGCACATGCCTGTAATCCCACCCACTCAGACTGAGGCAGGGAGAATT AAAATTAGCGGGCATGGTGGCACATGCCTGTATTCCCACCCACTCAGACTGAGGCAGGGAGAATT T A TNIP1 Ensembl:ENSG00000145901 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1186860181 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15603,RMVar_hsa_circ_89626,RMVar_hsa_circ_235527 25388 RMVar_ID_25388 Human_SNP_ID_256343612 A-to-I Human chr5 - 151054509 151054509 151054509 CTGGCCAATTTTTTGGTATTTTTAGTAGAGACAGGGTTTTGCCATGTTGCCCAGACTGGTGTTGA CTGGCCAATTTTTTGGTATTTTTAGTAGAGACGGGGTTTTGCCATGTTGCCCAGACTGGTGTTGA T C TNIP1 Ensembl:ENSG00000145901 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1317381000 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15603,RMVar_hsa_circ_89626,RMVar_hsa_circ_235527,RMVar_hsa_circ_58639,RMVar_hsa_circ_235530,RMVar_hsa_circ_349118,RMVar_hsa_circ_335155,RMVar_hsa_circ_24106,RMVar_hsa_circ_19862,RMVar_hsa_circ_2628 25389 RMVar_ID_25389 Human_SNP_ID_256343626 A-to-I Human chr5 - 151054555 151054555 151054555 CCTCAGTTCCCTGAATAGCTGAGACTACATGCATGCGCCCTTATGCCTGGCCAATTTTTTGGTAT CCTCAGTTCCCTGAATAGCTGAGACTACATGCCTGCGCCCTTATGCCTGGCCAATTTTTTGGTAT T G TNIP1 Ensembl:ENSG00000145901 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1364876586 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15603,RMVar_hsa_circ_89626,RMVar_hsa_circ_235527,RMVar_hsa_circ_58639,RMVar_hsa_circ_235530,RMVar_hsa_circ_349118,RMVar_hsa_circ_335155,RMVar_hsa_circ_24106,RMVar_hsa_circ_19862,RMVar_hsa_circ_2628 25390 RMVar_ID_25390 Human_SNP_ID_256344523 A-to-I Human chr5 - 151058045 151058045 151058045 GTAGTGGTGCACACCTGTAATCCCAGCTCCTCAGGAGCCTGAGGCAGGAGAATCGCTTGAACCCA GTAGTGGTGCACACCTGTAATCCCAGCTCCTCGGGAGCCTGAGGCAGGAGAATCGCTTGAACCCA T C TNIP1 Ensembl:ENSG00000145901 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1348463277 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15603,RMVar_hsa_circ_89626,RMVar_hsa_circ_235527,RMVar_hsa_circ_67248,RMVar_hsa_circ_235530,RMVar_hsa_circ_335155,RMVar_hsa_circ_24106,RMVar_hsa_circ_19862,RMVar_hsa_circ_296475 25391 RMVar_ID_25391 Human_SNP_ID_256355605 A-to-I Human chr5 - 151102617 151102617 151102617 TCACTGCAACGTCCACCTCCTGGGTTTAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGA TCACTGCAACGTCCACCTCCTGGGTTTAAGCAGTTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGA T C ANXA6 Ensembl:ENSG00000197043 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1463569091 Functional Loss SNV dbSNP153 33..33 33 - - - 25392 RMVar_ID_25392 Human_SNP_ID_256357920 A-to-I Human chr5 - 151111645 151111645 151111645 GGTCAAGGTTGCAGTGAGCCGAGATTGTGCCAATGTACTCCAGCCTGGGCAACAGAGCAAGACCC GGTCAAGGTTGCAGTGAGCCGAGATTGTGCCAGTGTACTCCAGCCTGGGCAACAGAGCAAGACCC T C ANXA6 Ensembl:ENSG00000197043 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs550908766 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17307,RMVar_hsa_circ_14800,RMVar_hsa_circ_49486,RMVar_hsa_circ_79861,RMVar_hsa_circ_87688,RMVar_hsa_circ_69720,RMVar_hsa_circ_102842,RMVar_hsa_circ_123405,RMVar_hsa_circ_235533,RMVar_hsa_circ_235534,RMVar_hsa_circ_320895,RMVar_hsa_circ_128126,RMVar_hsa_circ_110844,RMVar_hsa_circ_235538,RMVar_hsa_circ_235540,RMVar_hsa_circ_235539,RMVar_hsa_circ_235537,RMVar_hsa_circ_65293,RMVar_hsa_circ_288331,RMVar_hsa_circ_102581,RMVar_hsa_circ_235541 25393 RMVar_ID_25393 Human_SNP_ID_256358149 A-to-I Human chr5 - 151112644 151112644 151112644 AATTTTTTGGTAGAGTAGGGTTTCTCCACGTTATCCCGGCTGGTCTCAAACTCATAGGCTCAAGT AATTTTTTGGTAGAGTAGGGTTTCTCCACGTTTTCCCGGCTGGTCTCAAACTCATAGGCTCAAGT T A ANXA6 Ensembl:ENSG00000197043 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs867289444 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17307,RMVar_hsa_circ_14800,RMVar_hsa_circ_49486,RMVar_hsa_circ_79861,RMVar_hsa_circ_87688,RMVar_hsa_circ_69720,RMVar_hsa_circ_102842,RMVar_hsa_circ_123405,RMVar_hsa_circ_235533,RMVar_hsa_circ_235534,RMVar_hsa_circ_320895,RMVar_hsa_circ_128126,RMVar_hsa_circ_110844,RMVar_hsa_circ_235538,RMVar_hsa_circ_235540,RMVar_hsa_circ_235539,RMVar_hsa_circ_235537,RMVar_hsa_circ_65293,RMVar_hsa_circ_288331,RMVar_hsa_circ_102581,RMVar_hsa_circ_235541 25394 RMVar_ID_25394 Human_SNP_ID_256358187 A-to-I Human chr5 - 151112737 151112737 151112737 TCACTGCAACCTCCACCTTCTAGGCCCAAGCAATCCTCCCACCTCAGCCCCCCAAGTAGCTGGGA TCACTGCAACCTCCACCTTCTAGGCCCAAGCAGTCCTCCCACCTCAGCCCCCCAAGTAGCTGGGA T C ANXA6 Ensembl:ENSG00000197043 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1265199724 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17307,RMVar_hsa_circ_14800,RMVar_hsa_circ_49486,RMVar_hsa_circ_79861,RMVar_hsa_circ_87688,RMVar_hsa_circ_69720,RMVar_hsa_circ_102842,RMVar_hsa_circ_123405,RMVar_hsa_circ_235533,RMVar_hsa_circ_235534,RMVar_hsa_circ_320895,RMVar_hsa_circ_128126,RMVar_hsa_circ_110844,RMVar_hsa_circ_235538,RMVar_hsa_circ_235540,RMVar_hsa_circ_235539,RMVar_hsa_circ_235537,RMVar_hsa_circ_65293,RMVar_hsa_circ_288331,RMVar_hsa_circ_102581,RMVar_hsa_circ_235541 25395 RMVar_ID_25395 Human_SNP_ID_256359994 A-to-I Human chr5 - 151120028 151120028 151120028 AAAAAATACAAAAATTAGCCAAGCATGGTGGCATGCTTCTGTGGCCCCAGCTACTTGGGAGGCTG AAAAAATACAAAAATTAGCCAAGCATGGTGGCGTGCTTCTGTGGCCCCAGCTACTTGGGAGGCTG T C ANXA6 Ensembl:ENSG00000197043 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1333998347 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14800,RMVar_hsa_circ_79861,RMVar_hsa_circ_87688,RMVar_hsa_circ_123405,RMVar_hsa_circ_235533,RMVar_hsa_circ_235534,RMVar_hsa_circ_128126,RMVar_hsa_circ_110844,RMVar_hsa_circ_235538,RMVar_hsa_circ_235540,RMVar_hsa_circ_235539,RMVar_hsa_circ_288331,RMVar_hsa_circ_102581,RMVar_hsa_circ_235544,RMVar_hsa_circ_98572,RMVar_hsa_circ_235541,RMVar_hsa_circ_371039,RMVar_hsa_circ_127805,RMVar_hsa_circ_114604,RMVar_hsa_circ_117623,RMVar_hsa_circ_114309,RMVar_hsa_circ_235548,RMVar_hsa_circ_79109,RMVar_hsa_circ_79925,RMVar_hsa_circ_235549,RMVar_hsa_circ_235546,RMVar_hsa_circ_235547,RMVar_hsa_circ_235545,RMVar_hsa_circ_235542,RMVar_hsa_circ_235543,RMVar_hsa_circ_76263,RMVar_hsa_circ_235552 25396 RMVar_ID_25396 Human_SNP_ID_256367488 A-to-I Human chr5 - 151149631 151149631 151149631 AATACGAAAATTAGCCAGGTGTGGTGCCGTGCACCTGTAATCCCAGCTACTCAGGAGGCTGAGGC AATACGAAAATTAGCCAGGTGTGGTGCCGTGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGC T C ANXA6 Ensembl:ENSG00000197043 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs892610582 Functional Loss SNV dbSNP153 33..33 33 - - - 25397 RMVar_ID_25397 Human_SNP_ID_256367586 A-to-I Human chr5 - 151149997 151149997 151149997 CACCTGCCTCGGCCTCCTGACTAGCTGGGACTACAGGCACACACCATCACACCTGGCTAATTTTT CACCTGCCTCGGCCTCCTGACTAGCTGGGACTGCAGGCACACACCATCACACCTGGCTAATTTTT T C ANXA6 Ensembl:ENSG00000197043 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs141243524 Functional Loss SNV dbSNP153 33..33 33 - - - 25398 RMVar_ID_25398 Human_SNP_ID_256375113 A-to-I Human chr5 - 151181381 151181381 151181381 ACCCTGTCTCTACTAAAAAAATACAAAAAATTAGCTTGGCGTGGTGGTGGGCGCCTGTAGTCCCA ACCCTGTCTCTACTAAAAAAATACAAAAAATTCGCTTGGCGTGGTGGTGGGCGCCTGTAGTCCCA T G CCDC69 Ensembl:ENSG00000198624 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1347899610 Functional Loss SNV dbSNP153 33..33 33 - - - 25399 RMVar_ID_25399 Human_SNP_ID_256380485 A-to-I Human chr5 - 151203251 151203251 151203251 CTCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCATCGCGCCTGGCCTACATTTCC CTCACCTCGGCCTCCCAAAGTGCTGGGATTACGGGTGTGAGCCATCGCGCCTGGCCTACATTTCC T C CCDC69 Ensembl:ENSG00000198624 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1177708630 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56735,RMVar_hsa_circ_71097,RMVar_hsa_circ_350351 25400 RMVar_ID_25400 Human_SNP_ID_256380807 A-to-I Human chr5 - 151204308 151204308 151204308 TATCCAGGCCAGGTGCGGTGGCTCTTGCCTATAATCCCAGCACTTTGGGAGGCCAAGGTGGATGG TATCCAGGCCAGGTGCGGTGGCTCTTGCCTATGATCCCAGCACTTTGGGAGGCCAAGGTGGATGG T C CCDC69 Ensembl:ENSG00000198624 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs554809845 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56735,RMVar_hsa_circ_71097,RMVar_hsa_circ_350351 25401 RMVar_ID_25401 Human_SNP_ID_256382254 A-to-I Human chr5 - 151210717 151210717 151210717 GTGATCCTCCCGCCTCGGCCTCCTAAAGTGCTAGGATTACAGGTGTGAGCTACCACACCTAGCTG GTGATCCTCCCGCCTCGGCCTCCTAAAGTGCTGGGATTACAGGTGTGAGCTACCACACCTAGCTG T C CCDC69 Ensembl:ENSG00000198624 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs960496262 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_712007 25402 RMVar_ID_25402 Human_SNP_ID_256382507 A-to-I Human chr5 - 151211761 151211761 151211761 TCAGCACTTTGGGAGGCTGAGGTGGGTGGATCACTTGAAGTCAGGAGTTTGAGACCTGCCTGGCC TCAGCACTTTGGGAGGCTGAGGTGGGTGGATCGCTTGAAGTCAGGAGTTTGAGACCTGCCTGGCC T C CCDC69 Ensembl:ENSG00000198624 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs191676856 Functional Loss SNV dbSNP153 33..33 33 - - - 25403 RMVar_ID_25403 Human_SNP_ID_256396097 A-to-I Human chr5 + 151268176 151268174 151268177 TTGATTTCGATTTTTCGCTTTTTTTTTTTTTGAGACAGAATCTCACTTTGTCACCAGGCTGGAGT TTGATTTCGATTTTTCGCTTTTTTTTTTTTT___ACAGAATCTCACTTTGTCACCAGGCTGGAGT TGAG T GM2A Ensembl:ENSG00000196743 Protein coding 3'UTR GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 29129909,30559470 RNA-Seq:(High) rs1278808160 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_8213713,Human_RBP_ID_17575560,Human_RBP_ID_23313883,Human_RBP_ID_26523573 25404 RMVar_ID_25404 Human_SNP_ID_256396101 A-to-I Human chr5 + 151268176 151268176 151268176 TTGATTTCGATTTTTCGCTTTTTTTTTTTTTGAGACAGAATCTCACTTTGTCACCAGGCTGGAGT TTGATTTCGATTTTTCGCTTTTTTTTTTTTTGTGACAGAATCTCACTTTGTCACCAGGCTGGAGT A T GM2A Ensembl:ENSG00000196743 Protein coding 3'UTR GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 29129909,30559470 RNA-Seq:(High) rs1230168921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8213713,Human_RBP_ID_17575560,Human_RBP_ID_23313883,Human_RBP_ID_26523573 25405 RMVar_ID_25405 Human_SNP_ID_256396102 A-to-I Human chr5 + 151268178 151268178 151268178 GATTTCGATTTTTCGCTTTTTTTTTTTTTGAGACAGAATCTCACTTTGTCACCAGGCTGGAGTGC GATTTCGATTTTTCGCTTTTTTTTTTTTTGAGTCAGAATCTCACTTTGTCACCAGGCTGGAGTGC A T GM2A Ensembl:ENSG00000196743 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1288359519 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8213713,Human_RBP_ID_17575560,Human_RBP_ID_23313883,Human_RBP_ID_26523573 25406 RMVar_ID_25406 Human_SNP_ID_256396104 A-to-I Human chr5 + 151268188 151268188 151268188 TTTCGCTTTTTTTTTTTTTGAGACAGAATCTCACTTTGTCACCAGGCTGGAGTGCAGTGGTGCAA TTTCGCTTTTTTTTTTTTTGAGACAGAATCTCGCTTTGTCACCAGGCTGGAGTGCAGTGGTGCAA A G GM2A Ensembl:ENSG00000196743 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1405440586 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8213713,Human_RBP_ID_17575560,Human_RBP_ID_26529446 25407 RMVar_ID_25407 Human_SNP_ID_256396979 A-to-I Human chr5 + 151271961 151271961 151271961 AGCCAGGCGTGGTGGCACGTGCCTGTAATCCCAGCTACTCCGGAGGCTGAGGCAGGAGAATCGCT AGCCAGGCGTGGTGGCACGTGCCTGTAATCCCGGCTACTCCGGAGGCTGAGGCAGGAGAATCGCT A G RF00017-4751 RNACentral:URS000099F4EE SRP RNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs969536093 Functional Loss SNV dbSNP153 33..33 33 - - - 25408 RMVar_ID_25408 Human_SNP_ID_256466536 A-to-I Human chr5 - 151550210 151550210 151550210 GACTAGGGTCAGGCCAGCAAGGCATGCAGGACACAAAATGTAAGGAGGGCTCACTCTCTGGGCCA GACTAGGGTCAGGCCAGCAAGGCATGCAGGACCCAAAATGTAAGGAGGGCTCACTCTCTGGGCCA T G FAT2 Ensembl:ENSG00000086570 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs972620112 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2891,RMVar_hsa_circ_120969,RMVar_hsa_circ_235584,RMVar_hsa_circ_90273,RMVar_hsa_circ_235583 25409 RMVar_ID_25409 Human_SNP_ID_256511274 A-to-I Human chr5 - 151733242 151733242 151733242 CCTGTAATCCCAGCTACTCGGGAGGCTGAGACAGGAGAATCGCTTGAACCCAGGAGACGGAGATT CCTGTAATCCCAGCTACTCGGGAGGCTGAGACGGGAGAATCGCTTGAACCCAGGAGACGGAGATT T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs143463887 Functional Loss SNV dbSNP153 33..33 33 - - - 25410 RMVar_ID_25410 Human_SNP_ID_256514275 A-to-I Human chr5 - 151746810 151746810 151746810 ACAATCACTTGAACCCAGGAGGTGGAGGTTGCAGTGAGCTGAGATCATGCCACTGCACTCCAGCC ACAATCACTTGAACCCAGGAGGTGGAGGTTGCGGTGAGCTGAGATCATGCCACTGCACTCCAGCC T C ATOX1 Ensembl:ENSG00000177556 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1003440503 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69570,RMVar_hsa_circ_114971,RMVar_hsa_circ_235617,RMVar_hsa_circ_89655,RMVar_hsa_circ_235616 25411 RMVar_ID_25411 Human_SNP_ID_256514516 A-to-I Human chr5 - 151747662 151747662 151747662 AAGAATCGCTTGAACCCGGGAGTCAGGCTACAATGAGCTGAGATTGTGCCACTGCACTCCAGCCT AAGAATCGCTTGAACCCGGGAGTCAGGCTACAGTGAGCTGAGATTGTGCCACTGCACTCCAGCCT T C ATOX1 Ensembl:ENSG00000177556 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs928101632 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23313885 RMVar_hsa_circ_69570,RMVar_hsa_circ_114971,RMVar_hsa_circ_235617,RMVar_hsa_circ_89655,RMVar_hsa_circ_235616 25412 RMVar_ID_25412 Human_SNP_ID_256514572 A-to-I Human chr5 - 151747862 151747862 151747862 GAATAGGGCCGGGCACTGTGGCTCACGCCTATAGTCCCAACACTTTGGGAGGCCAATGCAGGTGG GAATAGGGCCGGGCACTGTGGCTCACGCCTATGGTCCCAACACTTTGGGAGGCCAATGCAGGTGG T C ATOX1 Ensembl:ENSG00000177556 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs533273780 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69570,RMVar_hsa_circ_114971,RMVar_hsa_circ_235617,RMVar_hsa_circ_89655,RMVar_hsa_circ_235616 25413 RMVar_ID_25413 Human_SNP_ID_256514573 A-to-I Human chr5 - 151747864 151747864 151747864 AAGAATAGGGCCGGGCACTGTGGCTCACGCCTATAGTCCCAACACTTTGGGAGGCCAATGCAGGT AAGAATAGGGCCGGGCACTGTGGCTCACGCCTGTAGTCCCAACACTTTGGGAGGCCAATGCAGGT T C ATOX1 Ensembl:ENSG00000177556 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1440688439 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69570,RMVar_hsa_circ_114971,RMVar_hsa_circ_235617,RMVar_hsa_circ_89655,RMVar_hsa_circ_235616 25414 RMVar_ID_25414 Human_SNP_ID_256514766 A-to-I Human chr5 - 151748785 151748785 151748785 ATGATCTTGGCTCACTGCAACCTCTGCCTCCCAGGTTCAAGTGATTCTCCTGCCCCAGCCTCCCG ATGATCTTGGCTCACTGCAACCTCTGCCTCCCGGGTTCAAGTGATTCTCCTGCCCCAGCCTCCCG T C ATOX1 Ensembl:ENSG00000177556 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1358357584 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69570,RMVar_hsa_circ_114971,RMVar_hsa_circ_235617,RMVar_hsa_circ_89655,RMVar_hsa_circ_235616 25415 RMVar_ID_25415 Human_SNP_ID_256515293 A-to-I Human chr5 - 151750725 151750725 151750725 GGAAGATCGCTTGAGCCTGGGAGGTTAAGGCCACAGTGAGCCTAGATCGTGCCACTGCACTGCAG GGAAGATCGCTTGAGCCTGGGAGGTTAAGGCCGCAGTGAGCCTAGATCGTGCCACTGCACTGCAG T C ATOX1 Ensembl:ENSG00000177556 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1326522985 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69570,RMVar_hsa_circ_114971,RMVar_hsa_circ_235617,RMVar_hsa_circ_89655,RMVar_hsa_circ_235616 25416 RMVar_ID_25416 Human_SNP_ID_256515306 A-to-I Human chr5 - 151750804 151750804 151750804 TCTACAAAAAATACCAAAAAAATTAGCCAGGCATGGTGTTACATGCCTGTACTCACAGCTAATTT TCTACAAAAAATACCAAAAAAATTAGCCAGGCTTGGTGTTACATGCCTGTACTCACAGCTAATTT T A ATOX1 Ensembl:ENSG00000177556 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs148917612 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69570,RMVar_hsa_circ_114971,RMVar_hsa_circ_235617,RMVar_hsa_circ_89655,RMVar_hsa_circ_235616 25417 RMVar_ID_25417 Human_SNP_ID_256515307 A-to-I Human chr5 - 151750804 151750804 151750804 TCTACAAAAAATACCAAAAAAATTAGCCAGGCATGGTGTTACATGCCTGTACTCACAGCTAATTT TCTACAAAAAATACCAAAAAAATTAGCCAGGCGTGGTGTTACATGCCTGTACTCACAGCTAATTT T C ATOX1 Ensembl:ENSG00000177556 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs148917612 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69570,RMVar_hsa_circ_114971,RMVar_hsa_circ_235617,RMVar_hsa_circ_89655,RMVar_hsa_circ_235616 25418 RMVar_ID_25418 Human_SNP_ID_256515502 A-to-I Human chr5 - 151751584 151751584 151751584 ATAACAGTAAAACTAAAATATATTGAGTACTTAGCACGTGCCAACTACTCTTGTTATTTTCTTAG ATAACAGTAAAACTAAAATATATTGAGTACTTCGCACGTGCCAACTACTCTTGTTATTTTCTTAG T G ATOX1 Ensembl:ENSG00000177556 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1341437328 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69570,RMVar_hsa_circ_114971,RMVar_hsa_circ_235617,RMVar_hsa_circ_89655,RMVar_hsa_circ_235616 25419 RMVar_ID_25419 Human_SNP_ID_256520198 A-to-I Human chr5 - 151769947 151769947 151769947 CCAGGATCTGCTAATTTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGG CCAGGATCTGCTAATTTTTTTGTATTTTTAGTTGAGACGGGGTTTCACCATGTTGGCCAGGCTGG T A ATOX1 Ensembl:ENSG00000177556 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1045866154 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_167956 25420 RMVar_ID_25420 Human_SNP_ID_256520199 A-to-I Human chr5 - 151769947 151769947 151769947 CCAGGATCTGCTAATTTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGG CCAGGATCTGCTAATTTTTTTGTATTTTTAGTGGAGACGGGGTTTCACCATGTTGGCCAGGCTGG T C ATOX1 Ensembl:ENSG00000177556 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1045866154 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_167956 25421 RMVar_ID_25421 Human_SNP_ID_256525785 A-to-I Human chr5 + 151789233 151789233 151789233 GAGAGGCTGAGGTGGGCGGATCACTTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAATATGGCAA GAGAGGCTGAGGTGGGCGGATCACTTGAGGTCGGGAGTTCAAGACCAGCCTGGCCAATATGGCAA A G G3BP1 Ensembl:ENSG00000145907 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs972345690 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25873391 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_34371,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_73757,RMVar_hsa_circ_235631 25422 RMVar_ID_25422 Human_SNP_ID_256529362 A-to-I Human chr5 + 151801834 151801834 151801834 AAGTTTTTTATTTTTTTATTTTTTTTTTTTTGAGACAGTGTCTCTCTCTGCCACCCAGGCTGGAG AAGTTTTTTATTTTTTTATTTTTTTTTTTTTGTGACAGTGTCTCTCTCTGCCACCCAGGCTGGAG A T G3BP1 Ensembl:ENSG00000145907 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs375345219 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15355625 RMVar_hsa_circ_84068,RMVar_hsa_circ_235621,RMVar_hsa_circ_235631,RMVar_hsa_circ_235643,RMVar_hsa_circ_112583 25423 RMVar_ID_25423 Human_SNP_ID_256529423 A-to-I Human chr5 + 151802017 151802017 151802017 TTTTGTATTTTTAGTAGACATGGGGCTTCCCCATGTTAACCAGGCTGATCTCGAACTCCTGACCT TTTTGTATTTTTAGTAGACATGGGGCTTCCCCGTGTTAACCAGGCTGATCTCGAACTCCTGACCT A G G3BP1 Ensembl:ENSG00000145907 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs543034506 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84068,RMVar_hsa_circ_235621,RMVar_hsa_circ_235631,RMVar_hsa_circ_235643,RMVar_hsa_circ_112583 25424 RMVar_ID_25424 Human_SNP_ID_256529632 A-to-I Human chr5 + 151802812 151802812 151802812 AAAATTAGCTGGGTGTGGTGGCGGACGCCTGTAGTCCCAGCTACTCGGGAGACTGAGGCAGGAGA AAAATTAGCTGGGTGTGGTGGCGGACGCCTGTCGTCCCAGCTACTCGGGAGACTGAGGCAGGAGA A C G3BP1 Ensembl:ENSG00000145907 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs555977347 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_165368 RMVar_hsa_circ_84068,RMVar_hsa_circ_235621,RMVar_hsa_circ_235631,RMVar_hsa_circ_235643,RMVar_hsa_circ_112583 25425 RMVar_ID_25425 Human_SNP_ID_257071899 A-to-I Human chr5 - 154000933 154000933 154000933 AAATCCCTTAGCATGGTGCCTGGCATAAAATTAGCACCCAGTAACTAATAACTAATAACTAATAA AAATCCCTTAGCATGGTGCCTGGCATAAAATTGGCACCCAGTAACTAATAACTAATAACTAATAA T C FAM114A2 Ensembl:ENSG00000055147 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs534627191 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27523,RMVar_hsa_circ_266587,RMVar_hsa_circ_329289,RMVar_hsa_circ_268279,RMVar_hsa_circ_40536,RMVar_hsa_circ_235665,RMVar_hsa_circ_281126,RMVar_hsa_circ_235664,RMVar_hsa_circ_6842,RMVar_hsa_circ_318444,RMVar_hsa_circ_355614,RMVar_hsa_circ_63721,RMVar_hsa_circ_83417,RMVar_hsa_circ_235666,RMVar_hsa_circ_235667 25426 RMVar_ID_25426 Human_SNP_ID_257160707 A-to-I Human chr5 + 154389542 154389542 154389542 AGGCAGAGGTTGCAGTGAGCCGAGATCGTGCCACTGCACTCTAATCTGGGCGACAAAGCGAGACT AGGCAGAGGTTGCAGTGAGCCGAGATCGTGCCGCTGCACTCTAATCTGGGCGACAAAGCGAGACT A G GALNT10 Ensembl:ENSG00000164574 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs948810052 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80848,RMVar_hsa_circ_235681,RMVar_hsa_circ_113233,RMVar_hsa_circ_235686,RMVar_hsa_circ_367957,RMVar_hsa_circ_117052,RMVar_hsa_circ_235689,RMVar_hsa_circ_87710,RMVar_hsa_circ_235691,RMVar_hsa_circ_100983,RMVar_hsa_circ_90616,RMVar_hsa_circ_235692,RMVar_hsa_circ_235693 25427 RMVar_ID_25427 Human_SNP_ID_257161617 A-to-I Human chr5 + 154393274 154393274 154393274 TTTTTAATATTTTGTAATGACAGGGTCTCCATATGTTGCCCAGGCTGGTCTCAAACTCCTGGCCT TTTTTAATATTTTGTAATGACAGGGTCTCCATGTGTTGCCCAGGCTGGTCTCAAACTCCTGGCCT A G GALNT10 Ensembl:ENSG00000164574 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1240924977 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_367957,RMVar_hsa_circ_87710,RMVar_hsa_circ_235691,RMVar_hsa_circ_90616,RMVar_hsa_circ_235693 25428 RMVar_ID_25428 Human_SNP_ID_257170762 A-to-I Human chr5 - 154432824 154432824 154432824 TTTGAGACTGGTCTTACTCTGTCACCCAGGCTAGTGTGCAATGGCACAATCATAGCTCACTGCAG TTTGAGACTGGTCTTACTCTGTCACCCAGGCTGGTGTGCAATGGCACAATCATAGCTCACTGCAG T C SAP30L-AS1 Ensembl:ENSG00000245275 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1231867169 Functional Loss SNV dbSNP153 33..33 33 - - - 25429 RMVar_ID_25429 Human_SNP_ID_257246119 A-to-I Human chr5 + 154736276 154736276 154736276 TGCCACCACACCTGGCTAATTTTTGTAGTTTTAGTGGACACGGGGTTTCACTATGTTGGCCAGGC TGCCACCACACCTGGCTAATTTTTGTAGTTTTGGTGGACACGGGGTTTCACTATGTTGGCCAGGC A G LARP1 Ensembl:ENSG00000155506 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1173275042 Functional Loss SNV dbSNP153 33..33 33 - - - 25430 RMVar_ID_25430 Human_SNP_ID_257246899 A-to-I Human chr5 + 154739599 154739599 154739599 TAAATTTTTTTTTGTAGACACAGGGTCTTGCTATGTTGACCAGGCTGATCTCACACTCCTGGCCT TAAATTTTTTTTTGTAGACACAGGGTCTTGCTGTGTTGACCAGGCTGATCTCACACTCCTGGCCT A G LARP1 Ensembl:ENSG00000155506 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965981787 Functional Loss SNV dbSNP153 33..33 33 - - - 25431 RMVar_ID_25431 Human_SNP_ID_257253533 A-to-I Human chr5 + 154765465 154765465 154765465 CAGCCTGCAGTGCAGCAGTGCAATCACGGCTCACTGCAGACTCAACCTCCCAGGCTCAAGTGATC CAGCCTGCAGTGCAGCAGTGCAATCACGGCTCGCTGCAGACTCAACCTCCCAGGCTCAAGTGATC A G LARP1 Ensembl:ENSG00000155506 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs553592276 Functional Loss SNV dbSNP153 33..33 33 - - - 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_117975,RMVar_hsa_circ_235699,RMVar_hsa_circ_235700 25432 RMVar_ID_25432 Human_SNP_ID_257257117 A-to-I Human chr5 + 154779572 154779572 154779572 CTGTTGTTGCCCAGACTGGAGTGCAGTGGCGCAATCTCGGCTCACCGCAACCTCCACCTCCCGGA CTGTTGTTGCCCAGACTGGAGTGCAGTGGCGCCATCTCGGCTCACCGCAACCTCCACCTCCCGGA A C LARP1 Ensembl:ENSG00000155506 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs564513829 Functional Loss SNV dbSNP153 33..33 33 - - - 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_117975,RMVar_hsa_circ_235699,RMVar_hsa_circ_235700 25433 RMVar_ID_25433 Human_SNP_ID_257259350 A-to-I Human chr5 + 154788956 154788956 154788956 AACTTTAGCCAGGCGTAGTGGCTGACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGTAG AACTTTAGCCAGGCGTAGTGGCTGACGCCTGTTATCCCAGCACTTTGGGAGGCTGAGGCAGGTAG A T LARP1 Ensembl:ENSG00000155506 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1340319070 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1941782,Human_miRNA_ID_1944828,Human_miRNA_ID_2085535,Human_miRNA_ID_2115973,Human_miRNA_ID_2199546,Human_miRNA_ID_2202613,Human_miRNA_ID_2315044,Human_miRNA_ID_2318204,Human_miRNA_ID_2321361,Human_miRNA_ID_2324518,Human_miRNA_ID_2327661,Human_miRNA_ID_2518897,Human_miRNA_ID_2522069,Human_miRNA_ID_2773905,Human_miRNA_ID_2815076,Human_miRNA_ID_2821263,Human_miRNA_ID_2827396,Human_miRNA_ID_2830546,Human_miRNA_ID_2834665,Human_miRNA_ID_2840029,Human_miRNA_ID_2845180,Human_miRNA_ID_2848202,Human_miRNA_ID_2862339,Human_miRNA_ID_3112065 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_117975,RMVar_hsa_circ_235699,RMVar_hsa_circ_235700 25434 RMVar_ID_25434 Human_SNP_ID_257265370 A-to-I Human chr5 + 154810551 154810551 154810551 ACTGTGTCACCTAGGCTGGAGTGCAGTGGCGCAATCTCGGCTCACTGCAACCTCCACCTCCCAGG ACTGTGTCACCTAGGCTGGAGTGCAGTGGCGCGATCTCGGCTCACTGCAACCTCCACCTCCCAGG A G LARP1 Ensembl:ENSG00000155506 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1176198650 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_65232,RMVar_hsa_circ_336714,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_235718,RMVar_hsa_circ_364265,RMVar_hsa_circ_119763,RMVar_hsa_circ_235719,RMVar_hsa_circ_22914,RMVar_hsa_circ_66210,RMVar_hsa_circ_235720,RMVar_hsa_circ_330057 25435 RMVar_ID_25435 Human_SNP_ID_257265406 A-to-I Human chr5 + 154810662 154810662 154810662 GGCACCCACCACCACACCTGGCTAATTTTTGTATTTTGGTAGAGATGGGGTTTCACCATGTTGGC GGCACCCACCACCACACCTGGCTAATTTTTGTGTTTTGGTAGAGATGGGGTTTCACCATGTTGGC A G LARP1 Ensembl:ENSG00000155506 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1243296683 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_65232,RMVar_hsa_circ_336714,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_235718,RMVar_hsa_circ_364265,RMVar_hsa_circ_119763,RMVar_hsa_circ_235719,RMVar_hsa_circ_22914,RMVar_hsa_circ_66210,RMVar_hsa_circ_235720,RMVar_hsa_circ_330057 25436 RMVar_ID_25436 Human_SNP_ID_257269912 A-to-I Human chr5 + 154827949 154827949 154827949 ATAGCTCACTGTAACCTCGACCTCCTGGGCTCAAGCAATCCTCCCGTCTCAGCTTCCCAAGTAGC ATAGCTCACTGTAACCTCGACCTCCTGGGCTCTAGCAATCCTCCCGTCTCAGCTTCCCAAGTAGC A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1561653913 Functional Loss SNV dbSNP153 33..33 33 - - - 25437 RMVar_ID_25437 Human_SNP_ID_257269981 A-to-I Human chr5 - 154828262 154828262 154828262 AACCCCACCAAGTGTGGTTGCTCACTACTGTAATCCCAAACTTTGGGAGGCTGAGCCAGAAGAAT AACCCCACCAAGTGTGGTTGCTCACTACTGTAGTCCCAAACTTTGGGAGGCTGAGCCAGAAGAAT T C FAXDC2 Ensembl:ENSG00000170271 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs538858903 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59249,RMVar_hsa_circ_91335,RMVar_hsa_circ_235724,RMVar_hsa_circ_66386,RMVar_hsa_circ_360490 25438 RMVar_ID_25438 Human_SNP_ID_257271971 A-to-I Human chr5 + 154836117 154836117 154836117 CTGGGGTTTTGCCATGTTGGCCAGGCTGGCCTAGAACTCTAAACCTCAAGCAATTCACCTGCCCC CTGGGGTTTTGCCATGTTGGCCAGGCTGGCCTTGAACTCTAAACCTCAAGCAATTCACCTGCCCC A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053054787 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15360072 25439 RMVar_ID_25439 Human_SNP_ID_257274208 A-to-I Human chr5 + 154845497 154845497 154845497 GGAAGTTGGACTGGGCATGGTGTCTCATGCCTATCATCCCAGCACTTTGAGAGGCTGAAGCGGGA GGAAGTTGGACTGGGCATGGTGTCTCATGCCTGTCATCCCAGCACTTTGAGAGGCTGAAGCGGGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1185347122 Functional Loss SNV dbSNP153 33..33 33 - - - 25440 RMVar_ID_25440 Human_SNP_ID_257279628 A-to-I Human chr5 + 154866226 154866226 154866226 CTTTGTCACCCAGGCTAGAGTGCAGTGGTGCTAACATGGCTTACTGCAGCCTCAATCTCCCAGGC CTTTGTCACCCAGGCTAGAGTGCAGTGGTGCTCACATGGCTTACTGCAGCCTCAATCTCCCAGGC A C CNOT8 Ensembl:ENSG00000155508 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1468056706 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_235727,RMVar_hsa_circ_274209,RMVar_hsa_circ_235726,RMVar_hsa_circ_81803,RMVar_hsa_circ_303656,RMVar_hsa_circ_337916,RMVar_hsa_circ_361054,RMVar_hsa_circ_350304,RMVar_hsa_circ_32748,RMVar_hsa_circ_37717,RMVar_hsa_circ_235728,RMVar_hsa_circ_235730 25441 RMVar_ID_25441 Human_SNP_ID_257279639 A-to-I Human chr5 + 154866266 154866266 154866266 TTACTGCAGCCTCAATCTCCCAGGCTTATCTGATCCTCCCACGTCAGCCCCCTAAGTAGCTGGGA TTACTGCAGCCTCAATCTCCCAGGCTTATCTGTTCCTCCCACGTCAGCCCCCTAAGTAGCTGGGA A T CNOT8 Ensembl:ENSG00000155508 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1484220903 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_235727,RMVar_hsa_circ_274209,RMVar_hsa_circ_235726,RMVar_hsa_circ_81803,RMVar_hsa_circ_303656,RMVar_hsa_circ_337916,RMVar_hsa_circ_361054,RMVar_hsa_circ_350304,RMVar_hsa_circ_32748,RMVar_hsa_circ_37717,RMVar_hsa_circ_235728,RMVar_hsa_circ_235730 25442 RMVar_ID_25442 Human_SNP_ID_257287610 A-to-I Human chr5 - 154896311 154896311 154896311 GGTCAGAGATTGGTGTTTTGCCTTCTGGAGCTACTGTCCAGGCATCTGGAGGAAAAGCAGCTTTC GGTCAGAGATTGGTGTTTTGCCTTCTGGAGCTGCTGTCCAGGCATCTGGAGGAAAAGCAGCTTTC T C GEMIN5 Ensembl:ENSG00000082516 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1377174411 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8893852 Human_Splice_Rec_714016 RMVar_hsa_circ_101768,RMVar_hsa_circ_119129,RMVar_hsa_circ_107630,RMVar_hsa_circ_111347,RMVar_hsa_circ_235732,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_289783,RMVar_hsa_circ_235738,RMVar_hsa_circ_235739 25443 RMVar_ID_25443 Human_SNP_ID_257294742 A-to-I Human chr5 - 154922968 154922968 154922968 TTTAAGGCCTGGCACGGTGGCTCACGCCTGTAATCCCAACACTTTGGGAGGCTGAGGCGGGCGGA TTTAAGGCCTGGCACGGTGGCTCACGCCTGTAGTCCCAACACTTTGGGAGGCTGAGGCGGGCGGA T C GEMIN5 Ensembl:ENSG00000082516 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1394525805 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119129,RMVar_hsa_circ_235732,RMVar_hsa_circ_77726,RMVar_hsa_circ_51513,RMVar_hsa_circ_304542,RMVar_hsa_circ_46683,RMVar_hsa_circ_93904,RMVar_hsa_circ_8208,RMVar_hsa_circ_235744,RMVar_hsa_circ_235745,RMVar_hsa_circ_127461,RMVar_hsa_circ_31150,RMVar_hsa_circ_345886,RMVar_hsa_circ_235747,RMVar_hsa_circ_349590,RMVar_hsa_circ_343816,RMVar_hsa_circ_78560,RMVar_hsa_circ_23861,RMVar_hsa_circ_91430,RMVar_hsa_circ_235748,RMVar_hsa_circ_235749,RMVar_hsa_circ_108542,RMVar_hsa_circ_39001,RMVar_hsa_circ_105632,RMVar_hsa_circ_235751,RMVar_hsa_circ_235750,RMVar_hsa_circ_87914,RMVar_hsa_circ_7093,RMVar_hsa_circ_323437,RMVar_hsa_circ_235754,RMVar_hsa_circ_235755,RMVar_hsa_circ_235756,RMVar_hsa_circ_325761,RMVar_hsa_circ_348111,RMVar_hsa_circ_311513,RMVar_hsa_circ_319532,RMVar_hsa_circ_96234,RMVar_hsa_circ_235757,RMVar_hsa_circ_235759,RMVar_hsa_circ_235760,RMVar_hsa_circ_235761,RMVar_hsa_circ_235758,RMVar_hsa_circ_75429,RMVar_hsa_circ_106720,RMVar_hsa_circ_71578,RMVar_hsa_circ_235762 25444 RMVar_ID_25444 Human_SNP_ID_257301030 A-to-I Human chr5 + 154946700 154946700 154946700 GCCAGGTGTGGGGTGCGGTGGTGCGTCCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGA GCCAGGTGTGGGGTGCGGTGGTGCGTCCCTGTGATCCCAGCTACTTGGGAGGCTGAGGCAGGAGA A G MRPL22 Ensembl:ENSG00000082515 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1317861952 Functional Loss SNV dbSNP153 33..33 33 - - - 25445 RMVar_ID_25445 Human_SNP_ID_257556714 A-to-I Human chr5 + 155983374 155983374 155983374 CAGGCTGGAGTGCAGTGGCATGATCTCGGCTCACTGCAACCTCCACCTCCCAGGTTCGAGTGATT CAGGCTGGAGTGCAGTGGCATGATCTCGGCTCGCTGCAACCTCCACCTCCCAGGTTCGAGTGATT A G SGCD Ensembl:ENSG00000170624 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1330722007 Functional Loss SNV dbSNP153 33..33 33 - - - 25446 RMVar_ID_25446 Human_SNP_ID_257844800 A-to-I Human chr5 - 157135458 157135458 157135458 ATATGGGGTATGGGCTGGGTACGGTGGCTCACACTTATAATCCTAGTGCTTTGGGAGGTTGATGT ATATGGGGTATGGGCTGGGTACGGTGGCTCACGCTTATAATCCTAGTGCTTTGGGAGGTTGATGT T C HAVCR2 Ensembl:ENSG00000135077 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1401422591 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7409568 25447 RMVar_ID_25447 Human_SNP_ID_257885081 A-to-I Human chr5 + 157298396 157298396 157298396 CTCTGTCGCTCAGGCTGGAGTGCGGTGACACTATCTCGGCTCACTGCAACTTCAGCCTCCTAGGT CTCTGTCGCTCAGGCTGGAGTGCGGTGACACTGTCTCGGCTCACTGCAACTTCAGCCTCCTAGGT A G CYFIP2 Ensembl:ENSG00000055163 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1045027027 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32668,RMVar_hsa_circ_310703,RMVar_hsa_circ_344306,RMVar_hsa_circ_350543,RMVar_hsa_circ_315149,RMVar_hsa_circ_291613,RMVar_hsa_circ_49501,RMVar_hsa_circ_85272,RMVar_hsa_circ_105418,RMVar_hsa_circ_15000,RMVar_hsa_circ_31847,RMVar_hsa_circ_115477,RMVar_hsa_circ_127813,RMVar_hsa_circ_105680,RMVar_hsa_circ_99611,RMVar_hsa_circ_101456,RMVar_hsa_circ_87019,RMVar_hsa_circ_235798,RMVar_hsa_circ_235802,RMVar_hsa_circ_35447,RMVar_hsa_circ_76709,RMVar_hsa_circ_22225,RMVar_hsa_circ_235803,RMVar_hsa_circ_235800,RMVar_hsa_circ_235801,RMVar_hsa_circ_235799,RMVar_hsa_circ_235796,RMVar_hsa_circ_235797,RMVar_hsa_circ_235795 25448 RMVar_ID_25448 Human_SNP_ID_257887866 A-to-I Human chr5 + 157309800 157309800 157309800 GCGACATGCAGATAGAGCTGGCCAGATACATTAAGACCAGTGCTCACTATGAAGAGAACAAGTCC GCGACATGCAGATAGAGCTGGCCAGATACATTGAGACCAGTGCTCACTATGAAGAGAACAAGTCC A G CYFIP2 Ensembl:ENSG00000055163 Protein coding CDS GSE56152 embryonic stem cells,wild type - 25708366 RNA-Seq:(High) rs3207362 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1648993,Human_RBP_ID_1991157,Human_RBP_ID_18837131,Human_RBP_ID_19124909 Human_Splice_Rec_714462,Human_Splice_Rec_714463,Human_Splice_Rec_714512,Human_Splice_Rec_714513,Human_Splice_Rec_714564,Human_Splice_Rec_714565,Human_Splice_Rec_714622,Human_Splice_Rec_714623,Human_Splice_Rec_714688,Human_Splice_Rec_714689,Human_Splice_Rec_714798,Human_Splice_Rec_714799 RMVar_hsa_circ_1015,RMVar_hsa_circ_32668,RMVar_hsa_circ_310703,RMVar_hsa_circ_344306,RMVar_hsa_circ_49501,RMVar_hsa_circ_85272,RMVar_hsa_circ_31847,RMVar_hsa_circ_115477,RMVar_hsa_circ_105680,RMVar_hsa_circ_99611,RMVar_hsa_circ_101456,RMVar_hsa_circ_87019,RMVar_hsa_circ_235798,RMVar_hsa_circ_76709,RMVar_hsa_circ_22225,RMVar_hsa_circ_235800,RMVar_hsa_circ_235801,RMVar_hsa_circ_235799,RMVar_hsa_circ_235796,RMVar_hsa_circ_235797,RMVar_hsa_circ_235795,RMVar_hsa_circ_348540 25449 RMVar_ID_25449 Human_SNP_ID_257887867 A-to-I Human chr5 + 157309800 157309800 157309800 GCGACATGCAGATAGAGCTGGCCAGATACATTAAGACCAGTGCTCACTATGAAGAGAACAAGTCC GCGACATGCAGATAGAGCTGGCCAGATACATTTAGACCAGTGCTCACTATGAAGAGAACAAGTCC A T CYFIP2 Ensembl:ENSG00000055163 Protein coding CDS GSE56152 embryonic stem cells,wild type - 25708366 RNA-Seq:(High) rs3207362 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1648993,Human_RBP_ID_1991157,Human_RBP_ID_18837131,Human_RBP_ID_19124909 Human_Splice_Rec_714462,Human_Splice_Rec_714463,Human_Splice_Rec_714512,Human_Splice_Rec_714513,Human_Splice_Rec_714564,Human_Splice_Rec_714565,Human_Splice_Rec_714622,Human_Splice_Rec_714623,Human_Splice_Rec_714688,Human_Splice_Rec_714689,Human_Splice_Rec_714798,Human_Splice_Rec_714799 RMVar_hsa_circ_1015,RMVar_hsa_circ_32668,RMVar_hsa_circ_310703,RMVar_hsa_circ_344306,RMVar_hsa_circ_49501,RMVar_hsa_circ_85272,RMVar_hsa_circ_31847,RMVar_hsa_circ_115477,RMVar_hsa_circ_105680,RMVar_hsa_circ_99611,RMVar_hsa_circ_101456,RMVar_hsa_circ_87019,RMVar_hsa_circ_235798,RMVar_hsa_circ_76709,RMVar_hsa_circ_22225,RMVar_hsa_circ_235800,RMVar_hsa_circ_235801,RMVar_hsa_circ_235799,RMVar_hsa_circ_235796,RMVar_hsa_circ_235797,RMVar_hsa_circ_235795,RMVar_hsa_circ_348540 25450 RMVar_ID_25450 Human_SNP_ID_257930835 A-to-I Human chr5 - 157477942 157477942 157477942 TCCTTTCAGCCTTGCTGACTTCTCCCTATAAAAGTAAAGCCTTTTTCTGCCCCAGCTCTGAGACA TCCTTTCAGCCTTGCTGACTTCTCCCTATAAAGGTAAAGCCTTTTTCTGCCCCAGCTCTGAGACA T C ADAM19 Ensembl:ENSG00000135074 Protein coding intron GSE107867;GSE123020:GSM3490832,GSM3490833,GSM3490834 ASD brains,Fragile X samples from UC Davis FXTAS brain repository;esophageal squamous carcinoma cells,KYSE180 cell line - 30559470,32596459 RNA-Seq:(High) rs993202781 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118709,RMVar_hsa_circ_235821,RMVar_hsa_circ_235822,RMVar_hsa_circ_76268 25451 RMVar_ID_25451 Human_SNP_ID_257930839 A-to-I Human chr5 - 157477957 157477957 157477957 CTGCTAGCCATAGATTCCTTTCAGCCTTGCTGACTTCTCCCTATAAAAGTAAAGCCTTTTTCTGC CTGCTAGCCATAGATTCCTTTCAGCCTTGCTGGCTTCTCCCTATAAAAGTAAAGCCTTTTTCTGC T C ADAM19 Ensembl:ENSG00000135074 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1138750 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_235770,Human_miRNA_ID_1371421 RMVar_hsa_circ_118709,RMVar_hsa_circ_235821,RMVar_hsa_circ_235822,RMVar_hsa_circ_76268 25452 RMVar_ID_25452 Human_SNP_ID_257930968 A-to-I Human chr5 - 157478397 157478397 157478397 CGATGGCAAGATCTGCAAGCGTCTCAAAGCCCAGGCAGAAAAGGACTTTTCTTTTATTGGAAGAA CGATGGCAAGATCTGCAAGCGTCTCAAAGCCCGGGCAGAAAAGGACTTTTCTTTTATTGGAAGAA T C ADAM19 Ensembl:ENSG00000135074 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1244990426 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118709,RMVar_hsa_circ_235821,RMVar_hsa_circ_235822,RMVar_hsa_circ_76268 25453 RMVar_ID_25453 Human_SNP_ID_257930969 A-to-I Human chr5 - 157478397 157478397 157478397 CGATGGCAAGATCTGCAAGCGTCTCAAAGCCCAGGCAGAAAAGGACTTTTCTTTTATTGGAAGAA CGATGGCAAGATCTGCAAGCGTCTCAAAGCCCCGGCAGAAAAGGACTTTTCTTTTATTGGAAGAA T G ADAM19 Ensembl:ENSG00000135074 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1244990426 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118709,RMVar_hsa_circ_235821,RMVar_hsa_circ_235822,RMVar_hsa_circ_76268 25454 RMVar_ID_25454 Human_SNP_ID_257995268 A-to-I Human chr5 + 157740753 157740753 157740753 GAGAAACCCCCGTCTCTACTAAAAATACAAAAAATTAGCTGGGCATGGTGGTGCATGCCTGTGAT GAGAAACCCCCGTCTCTACTAAAAATACAAAACATTAGCTGGGCATGGTGGTGCATGCCTGTGAT A C THG1L Ensembl:ENSG00000113272 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1207714670 Functional Loss SNV dbSNP153 33..33 33 - - - 25455 RMVar_ID_25455 Human_SNP_ID_257995276 A-to-I Human chr5 + 157740793 157740793 157740793 GGGCATGGTGGTGCATGCCTGTGATTCCAGCTACTTGGGAGGTTGAGGCAGGAGAATCATTTGAA GGGCATGGTGGTGCATGCCTGTGATTCCAGCTGCTTGGGAGGTTGAGGCAGGAGAATCATTTGAA A G THG1L Ensembl:ENSG00000113272 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs11550595 Functional Loss SNV dbSNP153 33..33 33 - - - 25456 RMVar_ID_25456 Human_SNP_ID_257999918 A-to-I Human chr5 + 157758214 157758214 157758214 TCAGCTCCCTGCAACTTCTGCCTCCCAGGTTCAAGCGATTCTCCTGCCTTAGCCTCCTGAGTAGC TCAGCTCCCTGCAACTTCTGCCTCCCAGGTTCGAGCGATTCTCCTGCCTTAGCCTCCTGAGTAGC A G LSM11 Ensembl:ENSG00000155858 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1470125204 Functional Loss SNV dbSNP153 33..33 33 - - - 25457 RMVar_ID_25457 Human_SNP_ID_257999936 A-to-I Human chr5 + 157758286 157758286 157758286 GCCACCATGGCTGACTCATTTTTTGTATTTTTAGTAGAGAAGGGGTTTTACCGTGTTAGCCAGGC GCCACCATGGCTGACTCATTTTTTGTATTTTTGGTAGAGAAGGGGTTTTACCGTGTTAGCCAGGC A G LSM11 Ensembl:ENSG00000155858 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1029275126 Functional Loss SNV dbSNP153 33..33 33 - - - 25458 RMVar_ID_25458 Human_SNP_ID_257999942 A-to-I Human chr5 + 157758311 157758311 157758311 TATTTTTAGTAGAGAAGGGGTTTTACCGTGTTAGCCAGGCTGGTCTTGAACTCCTGACCTTGGGT TATTTTTAGTAGAGAAGGGGTTTTACCGTGTTGGCCAGGCTGGTCTTGAACTCCTGACCTTGGGT A G LSM11 Ensembl:ENSG00000155858 Protein coding 3'UTR GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 ASD brains,Fragile X samples from NIH NeuroBioBank;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 30559470,31158229,31158229 RNA-Seq:(High) rs1310632628 Functional Loss SNV dbSNP153 33..33 33 - - - 25459 RMVar_ID_25459 Human_SNP_ID_258010391 A-to-I Human chr5 - 157801304 157801304 157801304 CAGGGTTTCTCCATGTTGGCCAGCTTGGTCTCAAACTCCTGACCTCAGGTGATCCACCTGTTTTG CAGGGTTTCTCCATGTTGGCCAGCTTGGTCTCGAACTCCTGACCTCAGGTGATCCACCTGTTTTG T C CLINT1 Ensembl:ENSG00000113282 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1269534117 Functional Loss SNV dbSNP153 33..33 33 - - - 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_349253,RMVar_hsa_circ_235863,RMVar_hsa_circ_123030,RMVar_hsa_circ_235862,RMVar_hsa_circ_127658,RMVar_hsa_circ_346953,RMVar_hsa_circ_235864 25460 RMVar_ID_25460 Human_SNP_ID_258017607 A-to-I Human chr5 - 157830961 157830961 157830961 TGTCTCACTGCAGCCTCAACCTCCCAGGCCCAAGCAGTCTTTCCACCTCAGCCCCACCCTCCACC TGTCTCACTGCAGCCTCAACCTCCCAGGCCCAGGCAGTCTTTCCACCTCAGCCCCACCCTCCACC T C CLINT1 Ensembl:ENSG00000113282 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886218600 Functional Loss SNV dbSNP153 33..33 33 - - - 25461 RMVar_ID_25461 Human_SNP_ID_258020243 A-to-I Human chr5 - 157840880 157840880 157840880 AAGAAAAAAATATATACACTTTTCTCTTTTTTAAAGAGATGGGGTCTCGCTGTGTTGCTCAGGCT AAGAAAAAAATATATACACTTTTCTCTTTTTTCAAGAGATGGGGTCTCGCTGTGTTGCTCAGGCT T G CLINT1 Ensembl:ENSG00000113282 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1162725716 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9173174,Human_RBP_ID_15363669 25462 RMVar_ID_25462 Human_SNP_ID_258022000 A-to-I Human chr5 - 157848235 157848235 157848235 AAAATTAGCCAGGGGTAGTGGCGGGCCCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGAATT AAAATTAGCCAGGGGTAGTGGCGGGCCCCTGTGGTCCCAGCTACTTGGGAGGCTGAGGCAGAATT T C CLINT1 Ensembl:ENSG00000113282 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1357642832 Functional Loss SNV dbSNP153 33..33 33 - - - 25463 RMVar_ID_25463 Human_SNP_ID_258043898 A-to-I Human chr5 - 157931373 157931373 157931373 CGTCATTGCCAAGAGTATTAGCAAGCTTGCCAATGTACCTGCTGGTGGGGCTGTGGCCGTCTCTG CGTCATTGCCAAGAGTATTAGCAAGCTTGCCAGTGTACCTGCTGGTGGGGCTGTGGCCGTCTCTG T C AC008677.2 Ensembl:ENSG00000244331 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879229452 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1833928,Human_miRNA_ID_1841410,Human_miRNA_ID_1862903,Human_miRNA_ID_1908637 25464 RMVar_ID_25464 Human_SNP_ID_258043900 A-to-I Human chr5 - 157931383 157931383 157931383 ACATTGAAGACGTCATTGCCAAGAGTATTAGCAAGCTTGCCAATGTACCTGCTGGTGGGGCTGTG ACATTGAAGACGTCATTGCCAAGAGTATTAGCCAGCTTGCCAATGTACCTGCTGGTGGGGCTGTG T G AC008677.2 Ensembl:ENSG00000244331 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs543310413 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1833928,Human_miRNA_ID_1841410 25465 RMVar_ID_25465 Human_SNP_ID_258043902 A-to-I Human chr5 - 157931386 157931386 157931386 AAAACATTGAAGACGTCATTGCCAAGAGTATTAGCAAGCTTGCCAATGTACCTGCTGGTGGGGCT AAAACATTGAAGACGTCATTGCCAAGAGTATTGGCAAGCTTGCCAATGTACCTGCTGGTGGGGCT T C AC008677.2 Ensembl:ENSG00000244331 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878959725 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1833928 25466 RMVar_ID_25466 Human_SNP_ID_258043904 A-to-I Human chr5 - 157931392 157931392 157931392 ATGGAAAAAACATTGAAGACGTCATTGCCAAGAGTATTAGCAAGCTTGCCAATGTACCTGCTGGT ATGGAAAAAACATTGAAGACGTCATTGCCAAGGGTATTAGCAAGCTTGCCAATGTACCTGCTGGT T C AC008677.2 Ensembl:ENSG00000244331 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878884134 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26827603,Human_RBP_ID_27077189 Human_miRNA_ID_1833928 25467 RMVar_ID_25467 Human_SNP_ID_258043914 A-to-I Human chr5 - 157931420 157931420 157931420 CGGCTCAACAAGGTTATTAGTGAGCTGAATGGAAAAAACATTGAAGACGTCATTGCCAAGAGTAT CGGCTCAACAAGGTTATTAGTGAGCTGAATGGCAAAAACATTGAAGACGTCATTGCCAAGAGTAT T G AC008677.2 Ensembl:ENSG00000244331 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1205993355 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26826790 25468 RMVar_ID_25468 Human_SNP_ID_258058449 A-to-I Human chr5 + 157987074 157987074 157987074 TCCATGAGTGCACATTTCTCCACCACCTCTAGATCAATGCACCAGATGACCAAGTAATTGGCTGT TCCATGAGTGCACATTTCTCCACCACCTCTAGGTCAATGCACCAGATGACCAAGTAATTGGCTGT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878962852 Functional Loss SNV dbSNP153 33..33 33 - - - 25469 RMVar_ID_25469 Human_SNP_ID_258354690 A-to-I Human chr5 - 159187528 159187528 159187528 GGTCAGGCATTCGAGACCAGCCTGGCCAACATAGTGAAACCCCGTATCTACTAAAAATACAAAAA GGTCAGGCATTCGAGACCAGCCTGGCCAACATGGTGAAACCCCGTATCTACTAAAAATACAAAAA T C RNF145 Ensembl:ENSG00000145860 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs553678137 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_235887,RMVar_hsa_circ_128083,RMVar_hsa_circ_55911,RMVar_hsa_circ_39412,RMVar_hsa_circ_316978,RMVar_hsa_circ_329924,RMVar_hsa_circ_337771 25470 RMVar_ID_25470 Human_SNP_ID_258355420 A-to-I Human chr5 - 159190180 159190180 159190180 AAAATTAACTGGGTGTGGTGGCATGCACTTTTAGTCCCAGCTACTTCGGAGGCTGAGGTGGAGGA AAAATTAACTGGGTGTGGTGGCATGCACTTTTGGTCCCAGCTACTTCGGAGGCTGAGGTGGAGGA T C RNF145 Ensembl:ENSG00000145860 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1019365939 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17575336,Human_RBP_ID_25875447 RMVar_hsa_circ_235887,RMVar_hsa_circ_128083,RMVar_hsa_circ_55911,RMVar_hsa_circ_39412,RMVar_hsa_circ_316978,RMVar_hsa_circ_329924,RMVar_hsa_circ_337771 25471 RMVar_ID_25471 Human_SNP_ID_258358653 A-to-I Human chr5 - 159203632 159203621 159203633 AATTTTAGGTCTTCTCCAAGAAAAAAAAAAAGAAAAAAAAAAACAACATGGCTGCAAAGGAGAAA AATTTTAGGTCTTCTCCAAGAAAAAAAAAAA____________CAACATGGCTGCAAAGGAGAAA GTTTTTTTTTTTC G RNF145 Ensembl:ENSG00000145860 Protein coding CDS GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1160934551 Functional Loss DEL dbSNP153 32..43 33 - - - Human_RBP_ID_4852228,Human_RBP_ID_23051390,Human_RBP_ID_25933094 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 25472 RMVar_ID_25472 Human_SNP_ID_258358671 A-to-I Human chr5 - 159203632 159203632 159203632 AATTTTAGGTCTTCTCCAAGAAAAAAAAAAAGAAAAAAAAAAACAACATGGCTGCAAAGGAGAAA AATTTTAGGTCTTCTCCAAGAAAAAAAAAAAGGAAAAAAAAAACAACATGGCTGCAAAGGAGAAA T C RNF145 Ensembl:ENSG00000145860 Protein coding CDS GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs765426233 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4852228,Human_RBP_ID_23051390,Human_RBP_ID_25933094 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 25473 RMVar_ID_25473 Human_SNP_ID_258551856 A-to-I Human chr5 + 160014407 160014407 160014407 GTCACATGGGCCAGGCATAGTGGCTCATTCCTATAATCCCAGCACTTGGGAGGCTGAGGCTGGAG GTCACATGGGCCAGGCATAGTGGCTCATTCCTGTAATCCCAGCACTTGGGAGGCTGAGGCTGGAG A G TTC1 Ensembl:ENSG00000113312 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1419659356 Functional Loss SNV dbSNP153 33..33 33 - - - 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_282804,RMVar_hsa_circ_235900,RMVar_hsa_circ_235902,RMVar_hsa_circ_235903,RMVar_hsa_circ_235901,RMVar_hsa_circ_235899 25474 RMVar_ID_25474 Human_SNP_ID_258552520 A-to-I Human chr5 + 160017240 160017240 160017240 AAAATTCTATCTTAGTGTGTTGGAGCTGCTATAACAAAATACCTTAGACTGGATAACTTATAAAT AAAATTCTATCTTAGTGTGTTGGAGCTGCTATGACAAAATACCTTAGACTGGATAACTTATAAAT A G TTC1 Ensembl:ENSG00000113312 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs955003490 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15365730 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_282804,RMVar_hsa_circ_235900,RMVar_hsa_circ_235902,RMVar_hsa_circ_235903,RMVar_hsa_circ_235901,RMVar_hsa_circ_235899 25475 RMVar_ID_25475 Human_SNP_ID_258569290 A-to-I Human chr5 - 160087176 160087176 160087176 CAAAGTCTCCCTTTGTTGCCCAGGCTGCTATCAAACTCCTGGGCTCAAGTGATCCTCTCGTCTTG CAAAGTCTCCCTTTGTTGCCCAGGCTGCTATCGAACTCCTGGGCTCAAGTGATCCTCTCGTCTTG T C PWWP2A Ensembl:ENSG00000170234 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1050637598 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_235911,RMVar_hsa_circ_235912,RMVar_hsa_circ_235914,RMVar_hsa_circ_309048,RMVar_hsa_circ_333086,RMVar_hsa_circ_235915 25476 RMVar_ID_25476 Human_SNP_ID_258573964 A-to-I Human chr5 - 160105382 160105382 160105382 AGGCGTGTGCCTCCGTGCCCGGCTAATTTTTTATATTTTTATTAGAGACAGGGTTTCACAGGATG AGGCGTGTGCCTCCGTGCCCGGCTAATTTTTTGTATTTTTATTAGAGACAGGGTTTCACAGGATG T C PWWP2A Ensembl:ENSG00000170234 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs918720125 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_167810,Human_RBP_ID_15366944 RMVar_hsa_circ_339732,RMVar_hsa_circ_338854 25477 RMVar_ID_25477 Human_SNP_ID_258574401 A-to-I Human chr5 - 160107102 160107102 160107102 CCGGTTAAGGCCGGTCACGGTGGCTCATGCCTATAAATCCCAGCACTTTGGGAGGCCAAGGTGGG CCGGTTAAGGCCGGTCACGGTGGCTCATGCCTGTAAATCCCAGCACTTTGGGAGGCCAAGGTGGG T C PWWP2A Ensembl:ENSG00000170234 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1030859941 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_339732,RMVar_hsa_circ_338854,RMVar_hsa_circ_367173 25478 RMVar_ID_25478 Human_SNP_ID_258574566 A-to-I Human chr5 - 160107892 160107892 160107892 GGTTCAAACAATTCTTGTGCCTCAGCCTTCCTAGTAGCTGGGATTTCAGGTGCCTGCCACCATAT GGTTCAAACAATTCTTGTGCCTCAGCCTTCCTGGTAGCTGGGATTTCAGGTGCCTGCCACCATAT T C PWWP2A Ensembl:ENSG00000170234 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1223232948 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_339732,RMVar_hsa_circ_338854,RMVar_hsa_circ_367173 25479 RMVar_ID_25479 Human_SNP_ID_258574572 A-to-I Human chr5 - 160107918 160107918 160107918 TGGCTCACTGGAACCTCCGCCTTTCGGGTTCAAACAATTCTTGTGCCTCAGCCTTCCTAGTAGCT TGGCTCACTGGAACCTCCGCCTTTCGGGTTCATACAATTCTTGTGCCTCAGCCTTCCTAGTAGCT T A PWWP2A Ensembl:ENSG00000170234 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946523654 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_339732,RMVar_hsa_circ_338854,RMVar_hsa_circ_367173 25480 RMVar_ID_25480 Human_SNP_ID_258574583 A-to-I Human chr5 - 160107939 160107939 160107939 CAGAGTGCAATGGTGCAATCTTGGCTCACTGGAACCTCCGCCTTTCGGGTTCAAACAATTCTTGT CAGAGTGCAATGGTGCAATCTTGGCTCACTGGCACCTCCGCCTTTCGGGTTCAAACAATTCTTGT T G PWWP2A Ensembl:ENSG00000170234 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1268378244 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_339732,RMVar_hsa_circ_338854,RMVar_hsa_circ_367173 25481 RMVar_ID_25481 Human_SNP_ID_258575368 A-to-I Human chr5 - 160110158 160110157 160110158 AAATTAGCCGGCTGTGGTGGTGTGTGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAAGAAAA AAATTAGCCGGCTGTGGTGGTGTGTGCCTGTA_TCCCAGCTACTCGGGAGGCTGAGGCAAGAAAA AT A PWWP2A Ensembl:ENSG00000170234 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1374979785 Functional Loss DEL dbSNP153 33..33 33 - - - 25482 RMVar_ID_25482 Human_SNP_ID_258575878 A-to-I Human chr5 - 160112040 160112040 160112040 TCACTGCAGCCTCAACCTCCTGGGCTCAAGCAATCCTCCCACATCAGCCTCCCAAATAGCTGCAG TCACTGCAGCCTCAACCTCCTGGGCTCAAGCAGTCCTCCCACATCAGCCTCCCAAATAGCTGCAG T C PWWP2A Ensembl:ENSG00000170234 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1302371869 Functional Loss SNV dbSNP153 33..33 33 - - - 25483 RMVar_ID_25483 Human_SNP_ID_258575976 A-to-I Human chr5 - 160112268 160112268 160112268 TGCAGTGAGCCGAGATCGCACCACTGCACTCTAGCCCGGATGACAGAGAGAGGCTCTTTCTAAAA TGCAGTGAGCCGAGATCGCACCACTGCACTCTGGCCCGGATGACAGAGAGAGGCTCTTTCTAAAA T C PWWP2A Ensembl:ENSG00000170234 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1290259934 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15367136 25484 RMVar_ID_25484 Human_SNP_ID_258576141 A-to-I Human chr5 - 160113011 160113011 160113011 GGGATTACAGGCGCACGCCACCAAGCCTGGCTAATTTTTTTGTATTTTTAGTAGAGACAGTGTTT GGGATTACAGGCGCACGCCACCAAGCCTGGCTGATTTTTTTGTATTTTTAGTAGAGACAGTGTTT T C PWWP2A Ensembl:ENSG00000170234 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs895079497 Functional Loss SNV dbSNP153 33..33 33 - - - 25485 RMVar_ID_25485 Human_SNP_ID_258576654 A-to-I Human chr5 - 160115054 160115054 160115054 CTCTCTGCATCCTCTGCGCCCCACCGGGTTCAAGTGATTCTTCTGCCTCAGCCTCCTGAGTAGCT CTCTCTGCATCCTCTGCGCCCCACCGGGTTCAGGTGATTCTTCTGCCTCAGCCTCCTGAGTAGCT T C PWWP2A Ensembl:ENSG00000170234 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1039340844 Functional Loss SNV dbSNP153 33..33 33 - - - 25486 RMVar_ID_25486 Human_SNP_ID_258576994 A-to-I Human chr5 - 160116124 160116124 160116124 CTTGAGCCCTGGAGGTGGAGGTTACAGTAGCTAAGATCACACAGTCCAGCCTGGGTGACAGAATG CTTGAGCCCTGGAGGTGGAGGTTACAGTAGCTGAGATCACACAGTCCAGCCTGGGTGACAGAATG T C PWWP2A Ensembl:ENSG00000170234 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1190589809 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17575574,Human_RBP_ID_25876045 25487 RMVar_ID_25487 Human_SNP_ID_258648546 A-to-I Human chr5 - 160387121 160387121 160387121 GCATTCTGCCTGCCTTGGCCTCCCAGAGTGCTAGTATTACAGATGTGAGCCACTGCTCCCAGCCA GCATTCTGCCTGCCTTGGCCTCCCAGAGTGCTGGTATTACAGATGTGAGCCACTGCTCCCAGCCA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1464531455 Functional Loss SNV dbSNP153 33..33 33 - - - 25488 RMVar_ID_25488 Human_SNP_ID_258883528 A-to-I Human chr5 - 161293580 161293580 161293580 TACTGAGATGATAATGGTGTCATGGGAAGATTATTCCCACTGGTTTCTAAAAGATTCTCTTGTGA TACTGAGATGATAATGGTGTCATGGGAAGATTTTTCCCACTGGTTTCTAAAAGATTCTCTTGTGA T A GABRB2 Ensembl:ENSG00000145864 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1211531306 Functional Loss SNV dbSNP153 33..33 33 - - - 25489 RMVar_ID_25489 Human_SNP_ID_258912950 A-to-I Human chr5 - 161421152 161421152 161421152 AAAACCCAACACTAGACAGAGCTGAATGCACTAAAGTGCCTAGAAAATAGCAATTAAGCAAATAC AAAACCCAACACTAGACAGAGCTGAATGCACTGAAGTGCCTAGAAAATAGCAATTAAGCAAATAC T C GABRB2 Ensembl:ENSG00000145864 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs887854200 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_31500,RMVar_hsa_circ_235934,RMVar_hsa_circ_297425 25490 RMVar_ID_25490 Human_SNP_ID_258937680 A-to-I Human chr5 - 161523494 161523494 161523494 TGTTGTAATTTCAGATGTAAGAAAAGCAGGAAAGTCAGCAATGAACTAATGTGGCCTGTCAGAGT TGTTGTAATTTCAGATGTAAGAAAAGCAGGAAGGTCAGCAATGAACTAATGTGGCCTGTCAGAGT T C GABRB2 Ensembl:ENSG00000145864 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs933354122 Functional Loss SNV dbSNP153 33..33 33 - - - 25491 RMVar_ID_25491 Human_SNP_ID_258937714 A-to-I Human chr5 - 161523643 161523643 161523643 ATTTCCAAAATTTGTACACTGAAATTATGGCTAGGGTTAAAAACTGAACCAAAGAACAGAGCCAA ATTTCCAAAATTTGTACACTGAAATTATGGCTGGGGTTAAAAACTGAACCAAAGAACAGAGCCAA T C GABRB2 Ensembl:ENSG00000145864 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1230430417 Functional Loss SNV dbSNP153 33..33 33 - - - 25492 RMVar_ID_25492 Human_SNP_ID_258940586 A-to-I Human chr5 - 161536360 161536360 161536360 TGACCACAGACAGCCTTAATTCCAAACAAATTATGCCCACACAATTTTGGGCACAATTTTGGCGA TGACCACAGACAGCCTTAATTCCAAACAAATTTTGCCCACACAATTTTGGGCACAATTTTGGCGA T A GABRB2 Ensembl:ENSG00000145864 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1006601478 Functional Loss SNV dbSNP153 33..33 33 - - - 25493 RMVar_ID_25493 Human_SNP_ID_259437294 A-to-I Human chr5 + 163445553 163445552 163445554 TTGGCTCATTGCAGCCTTGGCAGCCCAGGCTCAAGAGATCCTCCCACCTTAGCTTCCGAAATAGC TTGGCTCATTGCAGCCTTGGCAGCCCAGGCTC__GAGATCCTCCCACCTTAGCTTCCGAAATAGC CAA C CCNG1 Ensembl:ENSG00000113328 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs372156752 Functional Loss DEL dbSNP153 33..34 33 - - - 25494 RMVar_ID_25494 Human_SNP_ID_259437592 A-to-I Human chr5 + 163446909 163446908 163446910 TGGTGGCGCATGCCTGTAGTACCAGTTACTCCAGAGACTGAGGCAGGAGAATTGCTTGAACCTGT TGGTGGCGCATGCCTGTAGTACCAGTTACTCC__AGACTGAGGCAGGAGAATTGCTTGAACCTGT CAG C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934782283 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_15367878 25495 RMVar_ID_25495 Human_SNP_ID_259437595 A-to-I Human chr5 + 163446921 163446921 163446921 CCTGTAGTACCAGTTACTCCAGAGACTGAGGCAGGAGAATTGCTTGAACCTGTGAGGCAGTGAGA CCTGTAGTACCAGTTACTCCAGAGACTGAGGCGGGAGAATTGCTTGAACCTGTGAGGCAGTGAGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs536565627 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15367878 25496 RMVar_ID_25496 Human_SNP_ID_259442533 A-to-I Human chr5 + 163465701 163465701 163465701 GACAGCTGGGGGGCGCACAGTGGTTCACGCCTATAATCCCAGCACTTTGGGAGGCAAGGCAGGTG GACAGCTGGGGGGCGCACAGTGGTTCACGCCTGTAATCCCAGCACTTTGGGAGGCAAGGCAGGTG A G HMMR Ensembl:ENSG00000072571 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1170149288 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_235950,RMVar_hsa_circ_114318,RMVar_hsa_circ_266407 25497 RMVar_ID_25497 Human_SNP_ID_259442574 A-to-I Human chr5 + 163465857 163465857 163465857 GTGGCACGTGCCTGTAGTCCCAGCTACTTGGGAAGCTGAGGCAGGAGAATTGCTTGAACCTGGGA GTGGCACGTGCCTGTAGTCCCAGCTACTTGGGCAGCTGAGGCAGGAGAATTGCTTGAACCTGGGA A C HMMR Ensembl:ENSG00000072571 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1378645003 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_235950,RMVar_hsa_circ_114318,RMVar_hsa_circ_266407 25498 RMVar_ID_25498 Human_SNP_ID_259503501 A-to-I Human chr5 - 163709392 163709392 163709392 AGGAGTATTCCACCAAAGAAGAGAAATATGAAAAGGAGATGAAACTGCTGGAGGAGAAACTGAAG AGGAGTATTCCACCAAAGAAGAGAAATATGAAGAGGAGATGAAACTGCTGGAGGAGAAACTGAAG T C AC116917.1 Ensembl:ENSG00000224012 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs993200466 Functional Loss SNV dbSNP153 33..33 33 - - - 25499 RMVar_ID_25499 Human_SNP_ID_259503513 A-to-I Human chr5 - 163709452 163709452 163709452 AGTTGGAGGAGAAACTTCAAACCATGGACCAGACCGTCAAGTCCCTGATGGCCTCAGAGGAGGAG AGTTGGAGGAGAAACTTCAAACCATGGACCAGGCCGTCAAGTCCCTGATGGCCTCAGAGGAGGAG T C AC116917.1 Ensembl:ENSG00000224012 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1023611595 Functional Loss SNV dbSNP153 33..33 33 - - - 25500 RMVar_ID_25500 Human_SNP_ID_259503524 A-to-I Human chr5 - 163709493 163709493 163709493 AACAAAATTTTGAGCTAAGGTGGCCGAGAGCCAAGCCAGACAGTTGGAGGAGAAACTTCAAACCA AACAAAATTTTGAGCTAAGGTGGCCGAGAGCCGAGCCAGACAGTTGGAGGAGAAACTTCAAACCA T C AC116917.1 Ensembl:ENSG00000224012 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956142607 Functional Loss SNV dbSNP153 33..33 33 - - - 25501 RMVar_ID_25501 Human_SNP_ID_549782046 A-to-I Human chr14 + 30603072 30603072 30603072 AAAATAGGCCGGGCATCGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAAACCTAGGCGGGCGG AAAATAGGCCGGGCATCGTGGCTCACGCCTGTCATCCCAGCACTTTGGGAAACCTAGGCGGGCGG A C G2E3 Ensembl:ENSG00000092140 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1237041763 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17562368 RMVar_hsa_circ_375,RMVar_hsa_circ_50838,RMVar_hsa_circ_42713,RMVar_hsa_circ_17078,RMVar_hsa_circ_78747,RMVar_hsa_circ_298569,RMVar_hsa_circ_165496,RMVar_hsa_circ_331672,RMVar_hsa_circ_22109,RMVar_hsa_circ_27440,RMVar_hsa_circ_351551 25502 RMVar_ID_25502 Human_SNP_ID_549782084 A-to-I Human chr14 + 30603179 30603179 30603179 GAAACCCCGTCTCTATTAAAAATACAAAAATTAGCTGGGCATAGTGTTGTGCATCTGTAGTCCCA GAAACCCCGTCTCTATTAAAAATACAAAAATTGGCTGGGCATAGTGTTGTGCATCTGTAGTCCCA A G G2E3 Ensembl:ENSG00000092140 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1460401690 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_375,RMVar_hsa_circ_50838,RMVar_hsa_circ_42713,RMVar_hsa_circ_17078,RMVar_hsa_circ_78747,RMVar_hsa_circ_298569,RMVar_hsa_circ_165496,RMVar_hsa_circ_331672,RMVar_hsa_circ_22109,RMVar_hsa_circ_27440,RMVar_hsa_circ_351551 25503 RMVar_ID_25503 Human_SNP_ID_549782106 A-to-I Human chr14 + 30603232 30603232 30603232 TCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATTGCTTGAACCCAGGAGGCGGAGGTT TCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCCGGAGAATTGCTTGAACCCAGGAGGCGGAGGTT A C G2E3 Ensembl:ENSG00000092140 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1192666677 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_375,RMVar_hsa_circ_50838,RMVar_hsa_circ_42713,RMVar_hsa_circ_17078,RMVar_hsa_circ_78747,RMVar_hsa_circ_298569,RMVar_hsa_circ_165496,RMVar_hsa_circ_331672,RMVar_hsa_circ_22109,RMVar_hsa_circ_27440,RMVar_hsa_circ_351551 25504 RMVar_ID_25504 Human_SNP_ID_549782115 A-to-I Human chr14 + 30603275 30603275 30603275 TTGAACCCAGGAGGCGGAGGTTGCAGTCAGCCAAGGTCGCGCCACTGTACTCCAGCCTGGTGACA TTGAACCCAGGAGGCGGAGGTTGCAGTCAGCCGAGGTCGCGCCACTGTACTCCAGCCTGGTGACA A G G2E3 Ensembl:ENSG00000092140 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935083379 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_375,RMVar_hsa_circ_50838,RMVar_hsa_circ_42713,RMVar_hsa_circ_17078,RMVar_hsa_circ_78747,RMVar_hsa_circ_298569,RMVar_hsa_circ_165496,RMVar_hsa_circ_331672,RMVar_hsa_circ_22109,RMVar_hsa_circ_27440,RMVar_hsa_circ_351551 25505 RMVar_ID_25505 Human_SNP_ID_549784179 A-to-I Human chr14 + 30611711 30611711 30611711 ATAAGGTCTCAGTCTGTCACCCAGGCTGGAGTACATTGGTGTGATCATAGCTCACTGAACCTCCA ATAAGGTCTCAGTCTGTCACCCAGGCTGGAGTGCATTGGTGTGATCATAGCTCACTGAACCTCCA A G G2E3 Ensembl:ENSG00000092140 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1178513092 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_375,RMVar_hsa_circ_50838,RMVar_hsa_circ_17078,RMVar_hsa_circ_331672,RMVar_hsa_circ_22109,RMVar_hsa_circ_27440,RMVar_hsa_circ_301997,RMVar_hsa_circ_366198 25506 RMVar_ID_25506 Human_SNP_ID_549784197 A-to-I Human chr14 + 30611788 30611788 30611788 AAAATCCTTCTACCTCATCTTCCAGAGTAGCTAGGACTACAGGTGTATACCACCCACACCAGGCC AAAATCCTTCTACCTCATCTTCCAGAGTAGCTGGGACTACAGGTGTATACCACCCACACCAGGCC A G G2E3 Ensembl:ENSG00000092140 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017871709 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_375,RMVar_hsa_circ_50838,RMVar_hsa_circ_17078,RMVar_hsa_circ_331672,RMVar_hsa_circ_22109,RMVar_hsa_circ_27440,RMVar_hsa_circ_301997,RMVar_hsa_circ_366198 25507 RMVar_ID_25507 Human_SNP_ID_549832845 A-to-I Human chr14 + 30821492 30821492 30821492 AAGTGGTGTTTGTCCTGGCTGGATGCTACTCCAGACACAAAGCTGTCATCGTGAAGAACATTGAT AAGTGGTGTTTGTCCTGGCTGGATGCTACTCCGGACACAAAGCTGTCATCGTGAAGAACATTGAT A G AL049830.1 Ensembl:ENSG00000213867 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs774732440 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26432492 Human_miRNA_ID_1887584,Human_miRNA_ID_1897683 25508 RMVar_ID_25508 Human_SNP_ID_549832846 A-to-I Human chr14 + 30821496 30821496 30821496 GGTGTTTGTCCTGGCTGGATGCTACTCCAGACACAAAGCTGTCATCGTGAAGAACATTGATGATG GGTGTTTGTCCTGGCTGGATGCTACTCCAGACGCAAAGCTGTCATCGTGAAGAACATTGATGATG A G AL049830.1 Ensembl:ENSG00000213867 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs112733816 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1492593,Human_RBP_ID_1817639,Human_RBP_ID_4312027,Human_RBP_ID_5175920,Human_RBP_ID_22923116,Human_RBP_ID_26432492,Human_RBP_ID_26923453,Human_RBP_ID_27226115 Human_miRNA_ID_1897683 25509 RMVar_ID_25509 Human_SNP_ID_549855029 A-to-I Human chr14 - 30909618 30909618 30909618 TAAAGATTTGCCAGATGGGGTGTCACATGCCTATAGTCCCAGACACTCGGGAGGCTGAGCTGGGA TAAAGATTTGCCAGATGGGGTGTCACATGCCTGTAGTCCCAGACACTCGGGAGGCTGAGCTGGGA T C STRN3 Ensembl:ENSG00000196792 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982487020 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17562373 RMVar_hsa_circ_6881,RMVar_hsa_circ_269329,RMVar_hsa_circ_165557,RMVar_hsa_circ_54381,RMVar_hsa_circ_280736,RMVar_hsa_circ_359573,RMVar_hsa_circ_372471,RMVar_hsa_circ_306418,RMVar_hsa_circ_274293,RMVar_hsa_circ_165559,RMVar_hsa_circ_165558,RMVar_hsa_circ_165561,RMVar_hsa_circ_337749,RMVar_hsa_circ_165556,RMVar_hsa_circ_377597,RMVar_hsa_circ_315798,RMVar_hsa_circ_80801,RMVar_hsa_circ_165560,RMVar_hsa_circ_364373,RMVar_hsa_circ_64825,RMVar_hsa_circ_165562 25510 RMVar_ID_25510 Human_SNP_ID_549858187 A-to-I Human chr14 - 30922135 30922135 30922135 CCTGTGGTCCCAGCTACTCTGGAGACTGAGGTAGGTGGATTGCCTGAGCCTAAGAGTTCAAGACC CCTGTGGTCCCAGCTACTCTGGAGACTGAGGTGGGTGGATTGCCTGAGCCTAAGAGTTCAAGACC T C STRN3 Ensembl:ENSG00000196792 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1268144718 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6339063,Human_RBP_ID_12311365,Human_RBP_ID_21968963 RMVar_hsa_circ_54381,RMVar_hsa_circ_359573,RMVar_hsa_circ_165559,RMVar_hsa_circ_165561,RMVar_hsa_circ_337749,RMVar_hsa_circ_377597,RMVar_hsa_circ_315798,RMVar_hsa_circ_165560,RMVar_hsa_circ_364373,RMVar_hsa_circ_68997,RMVar_hsa_circ_375836,RMVar_hsa_circ_293862,RMVar_hsa_circ_309216,RMVar_hsa_circ_165563,RMVar_hsa_circ_330311,RMVar_hsa_circ_62803,RMVar_hsa_circ_43621,RMVar_hsa_circ_165564,RMVar_hsa_circ_165565,RMVar_hsa_circ_363115,RMVar_hsa_circ_114945,RMVar_hsa_circ_299679,RMVar_hsa_circ_165566,RMVar_hsa_circ_285390,RMVar_hsa_circ_165568,RMVar_hsa_circ_165569 25511 RMVar_ID_25511 Human_SNP_ID_549863637 A-to-I Human chr14 - 30943478 30943478 30943478 CTCCCACTTCAGCCTCCAGAGTAGCTGGGACTACAGCCACATGCCACCACACCTGGCTGATTCTT CTCCCACTTCAGCCTCCAGAGTAGCTGGGACTCCAGCCACATGCCACCACACCTGGCTGATTCTT T G STRN3 Ensembl:ENSG00000196792 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs938220591 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_359573,RMVar_hsa_circ_165559,RMVar_hsa_circ_165561,RMVar_hsa_circ_315798,RMVar_hsa_circ_364373,RMVar_hsa_circ_293862,RMVar_hsa_circ_309216,RMVar_hsa_circ_330311,RMVar_hsa_circ_165564,RMVar_hsa_circ_165565,RMVar_hsa_circ_363115,RMVar_hsa_circ_285390,RMVar_hsa_circ_31399,RMVar_hsa_circ_165571,RMVar_hsa_circ_165569,RMVar_hsa_circ_272912,RMVar_hsa_circ_165572,RMVar_hsa_circ_302699,RMVar_hsa_circ_277971,RMVar_hsa_circ_373140,RMVar_hsa_circ_300123,RMVar_hsa_circ_165574,RMVar_hsa_circ_165573,RMVar_hsa_circ_16290 25512 RMVar_ID_25512 Human_SNP_ID_549877183 A-to-I Human chr14 - 30993776 30993776 30993776 ACTCAGGAGGCTAAGGCAGGAGAATTGCTTGAACCTGCGAGGCCGAGGTTGCAGTGAGCCGAGAT ACTCAGGAGGCTAAGGCAGGAGAATTGCTTGACCCTGCGAGGCCGAGGTTGCAGTGAGCCGAGAT T G STRN3 Ensembl:ENSG00000196792 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1370046063 Functional Loss SNV dbSNP153 33..33 33 - - - 25513 RMVar_ID_25513 Human_SNP_ID_549877311 A-to-I Human chr14 - 30994263 30994263 30994263 ATTGGGCTGGGTGGCCGTGGCTCATGCCTGTAATCCTAGAACTTTGGGAGGCTGAGGCAGGCAAA ATTGGGCTGGGTGGCCGTGGCTCATGCCTGTAGTCCTAGAACTTTGGGAGGCTGAGGCAGGCAAA T C STRN3 Ensembl:ENSG00000196792 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1488261121 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12312561,Human_RBP_ID_17562390 25514 RMVar_ID_25514 Human_SNP_ID_549881415 A-to-I Human chr14 - 31010020 31010020 31010020 TGGCTCACTGTAGCTTTGTCCTTCTGGGCTCAAGCAATCCTCCTGCCTCAGCCTCCTCAGAAGCA TGGCTCACTGTAGCTTTGTCCTTCTGGGCTCAGGCAATCCTCCTGCCTCAGCCTCCTCAGAAGCA T C STRN3 Ensembl:ENSG00000196792 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs555113893 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12313159 25515 RMVar_ID_25515 Human_SNP_ID_549881630 A-to-I Human chr14 - 31010866 31010866 31010866 CCTGGCTAATTTTTGTATTTTTAGGAAAGACAAGGTTTCGCCATGTCGGCTAGGCTGGTCTCGAA CCTGGCTAATTTTTGTATTTTTAGGAAAGACAGGGTTTCGCCATGTCGGCTAGGCTGGTCTCGAA T C STRN3 Ensembl:ENSG00000196792 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1431808878 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12313182 25516 RMVar_ID_25516 Human_SNP_ID_549882214 A-to-I Human chr14 - 31013146 31013146 31013146 TCCTCCCACCTCAGCCTCCAAAGTTTGGGACTACAGGAACATGCCTCCACACCTGACTAATTTTG TCCTCCCACCTCAGCCTCCAAAGTTTGGGACTTCAGGAACATGCCTCCACACCTGACTAATTTTG T A STRN3 Ensembl:ENSG00000196792 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1219265442 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12313268 25517 RMVar_ID_25517 Human_SNP_ID_549884029 A-to-I Human chr14 - 31019186 31019186 31019186 CTCCCACTTCAGCCTCCCAAATAGCTTGGACTATAGGCACGTGCTACCACGCCTGGCTAATTTTT CTCCCACTTCAGCCTCCCAAATAGCTTGGACTGTAGGCACGTGCTACCACGCCTGGCTAATTTTT T C STRN3 Ensembl:ENSG00000196792 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941112084 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12313464 RMVar_hsa_circ_165581 25518 RMVar_ID_25518 Human_SNP_ID_549893945 A-to-I Human chr14 + 31056428 31056428 31056428 TCGCCCAGGCTGGAGTGCAGTGGCGCGATCTCAGCTCACTGCAACCTCCGCCTCCTGGGTTCGGG TCGCCCAGGCTGGAGTGCAGTGGCGCGATCTCGGCTCACTGCAACCTCCGCCTCCTGGGTTCGGG A G AP4S1 Ensembl:ENSG00000100478 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1183920299 Functional Loss SNV dbSNP153 33..33 33 - - - 25519 RMVar_ID_25519 Human_SNP_ID_549893960 A-to-I Human chr14 + 31056476 31056476 31056476 CGCCTCCTGGGTTCGGGCGATTCTCCTGCCTCAGCCTCCTAAGTAGCTAGGATTACAGGTGTCCG CGCCTCCTGGGTTCGGGCGATTCTCCTGCCTCGGCCTCCTAAGTAGCTAGGATTACAGGTGTCCG A G AP4S1 Ensembl:ENSG00000100478 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042019122 Functional Loss SNV dbSNP153 33..33 33 - - - 25520 RMVar_ID_25520 Human_SNP_ID_549899430 A-to-I Human chr14 + 31077095 31077095 31077095 GGGATTACAGGCATGCGCCACCACGCCTGGCTAATTTTTGTATTATTAGTAGAGACAGGGTTTCT GGGATTACAGGCATGCGCCACCACGCCTGGCTCATTTTTGTATTATTAGTAGAGACAGGGTTTCT A C AP4S1 Ensembl:ENSG00000100478 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946497961 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43849,RMVar_hsa_circ_165582 25521 RMVar_ID_25521 Human_SNP_ID_549901578 A-to-I Human chr14 + 31085650 31085650 31085650 TTTAAAAAGCCAGGCATTGGTGGTGTGTGCCTATAGTCCCAACTACTAGGGAGGCTGAGGTGGGA TTTAAAAAGCCAGGCATTGGTGGTGTGTGCCTGTAGTCCCAACTACTAGGGAGGCTGAGGTGGGA A G AP4S1 Ensembl:ENSG00000100478 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1347865540 Functional Loss SNV dbSNP153 33..33 33 - - - 25522 RMVar_ID_25522 Human_SNP_ID_549901585 A-to-I Human chr14 + 31085688 31085688 31085688 CCAACTACTAGGGAGGCTGAGGTGGGAGGATCACTTGAGCCTGGGGGACTGAGGCTGCAGTGAGC CCAACTACTAGGGAGGCTGAGGTGGGAGGATCCCTTGAGCCTGGGGGACTGAGGCTGCAGTGAGC A C AP4S1 Ensembl:ENSG00000100478 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1192213309 Functional Loss SNV dbSNP153 33..33 33 - - - 25523 RMVar_ID_25523 Human_SNP_ID_549903407 A-to-I Human chr14 + 31093568 31093568 31093568 CACTTCCGGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCGAGCTGGGACTACAGGCATGCACCAC CACTTCCGGGGTTCAAGCGATTCTCCTGCCTCTGCCTCCGAGCTGGGACTACAGGCATGCACCAC A T AP4S1 Ensembl:ENSG00000100478 Protein coding 3'UTR GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1439043228 Functional Loss SNV dbSNP153 33..33 33 - - - 25524 RMVar_ID_25524 Human_SNP_ID_549903424 A-to-I Human chr14 + 31093636 31093635 31093637 ACCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGTCTCAAA ACCTGGCTAATTTTTGTATTTTTAGTAGAGAC__GGTTTCACCATGTTGGCCAGGCTGTCTCAAA CAG C AP4S1 Ensembl:ENSG00000100478 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs781711129 Functional Loss DEL dbSNP153 33..34 33 - - - 25525 RMVar_ID_25525 Human_SNP_ID_549903432 A-to-I Human chr14 + 31093666 31093666 31093666 ACAGGGTTTCACCATGTTGGCCAGGCTGTCTCAAACTCCTGACCTCAGGTGATCTGCCTGCCTCA ACAGGGTTTCACCATGTTGGCCAGGCTGTCTCGAACTCCTGACCTCAGGTGATCTGCCTGCCTCA A G AP4S1 Ensembl:ENSG00000100478 Protein coding 3'UTR GSE47997;GSE107867 K562 cells&HepG2 cells;ASD brains,frontal_cortex - 23474544,30559470 RNA-Seq:(High) rs1352986177 Functional Loss SNV dbSNP153 33..33 33 - - - 25526 RMVar_ID_25526 Human_SNP_ID_549903433 A-to-I Human chr14 + 31093666 31093666 31093666 ACAGGGTTTCACCATGTTGGCCAGGCTGTCTCAAACTCCTGACCTCAGGTGATCTGCCTGCCTCA ACAGGGTTTCACCATGTTGGCCAGGCTGTCTCTAACTCCTGACCTCAGGTGATCTGCCTGCCTCA A T AP4S1 Ensembl:ENSG00000100478 Protein coding 3'UTR GSE47997;GSE107867 K562 cells&HepG2 cells;ASD brains,frontal_cortex - 23474544,30559470 RNA-Seq:(High) rs1352986177 Functional Loss SNV dbSNP153 33..33 33 - - - 25527 RMVar_ID_25527 Human_SNP_ID_549903480 A-to-I Human chr14 + 31093930 31093930 31093930 CCACCTCTGGGTTTAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCTGCGACTACAGGCATGTA CCACCTCTGGGTTTAAGCAATTCTCCTGCCTCCGCCTCCTGAGTAGCTGCGACTACAGGCATGTA A C AP4S1 Ensembl:ENSG00000100478 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1198517108 Functional Loss SNV dbSNP153 33..33 33 - - - 25528 RMVar_ID_25528 Human_SNP_ID_549903593 A-to-I Human chr14 + 31094504 31094501 31094504 TGTAGTCTCAACTACTCGGGAGTCTGAGGCAGAAGATTTCTTGAGCCCAGGAGTTCGAGTCTGCA TGTAGTCTCAACTACTCGGGAGTCTGAGGC___AGATTTCTTGAGCCCAGGAGTTCGAGTCTGCA CAGA C AP4S1 Ensembl:ENSG00000100478 Protein coding 3'UTR GSE100210;GSE107867 HepG2 cell line;ASD brains,frontal_cortex - 29129909,30559470 RNA-Seq:(High) rs754385701 Functional Loss DEL dbSNP153 31..33 33 - - - 25529 RMVar_ID_25529 Human_SNP_ID_549903623 A-to-I Human chr14 + 31094633 31094633 31094633 AAAAAAGTCCGAGTGCGGTGGCTCAGGCCTGTAATCCCAACATTTTGGGGGGCCAAGCCAGGAGG AAAAAAGTCCGAGTGCGGTGGCTCAGGCCTGTGATCCCAACATTTTGGGGGGCCAAGCCAGGAGG A G AP4S1 Ensembl:ENSG00000100478 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs779979366 Functional Loss SNV dbSNP153 33..33 33 - - - 25530 RMVar_ID_25530 Human_SNP_ID_549903682 A-to-I Human chr14 + 31094895 31094895 31094895 AAAGTTAGCCAGGCATGGTGGCAAGCACCTCTAATCTCAGCTACTCAGGAGGCTGAGGCAGTAGA AAAGTTAGCCAGGCATGGTGGCAAGCACCTCTGATCTCAGCTACTCAGGAGGCTGAGGCAGTAGA A G AP4S1 Ensembl:ENSG00000100478 Protein coding 3'UTR GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs545198645 Functional Loss SNV dbSNP153 33..33 33 - - - 25531 RMVar_ID_25531 Human_SNP_ID_549903683 A-to-I Human chr14 + 31094895 31094895 31094895 AAAGTTAGCCAGGCATGGTGGCAAGCACCTCTAATCTCAGCTACTCAGGAGGCTGAGGCAGTAGA AAAGTTAGCCAGGCATGGTGGCAAGCACCTCTTATCTCAGCTACTCAGGAGGCTGAGGCAGTAGA A T AP4S1 Ensembl:ENSG00000100478 Protein coding 3'UTR GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs545198645 Functional Loss SNV dbSNP153 33..33 33 - - - 25532 RMVar_ID_25532 Human_SNP_ID_549903714 A-to-I Human chr14 + 31095073 31095073 31095073 AAAGTTAGCCAGCTGTGGTGGTGAGCACCTGTACTCCTAACTACTCAAGAGGCTGAGATGGGAGA AAAGTTAGCCAGCTGTGGTGGTGAGCACCTGTGCTCCTAACTACTCAAGAGGCTGAGATGGGAGA A G AP4S1 Ensembl:ENSG00000100478 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1201368593 Functional Loss SNV dbSNP153 33..33 33 - - - 25533 RMVar_ID_25533 Human_SNP_ID_549903724 A-to-I Human chr14 + 31095113 31095113 31095113 CTACTCAAGAGGCTGAGATGGGAGAATTGATCAAGCCTAGGAGTTTGAGGCTGCAGTGAACTATG CTACTCAAGAGGCTGAGATGGGAGAATTGATCCAGCCTAGGAGTTTGAGGCTGCAGTGAACTATG A C AP4S1 Ensembl:ENSG00000100478 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1303683343 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6339891 25534 RMVar_ID_25534 Human_SNP_ID_549903725 A-to-I Human chr14 + 31095113 31095113 31095113 CTACTCAAGAGGCTGAGATGGGAGAATTGATCAAGCCTAGGAGTTTGAGGCTGCAGTGAACTATG CTACTCAAGAGGCTGAGATGGGAGAATTGATCGAGCCTAGGAGTTTGAGGCTGCAGTGAACTATG A G AP4S1 Ensembl:ENSG00000100478 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1303683343 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6339891 25535 RMVar_ID_25535 Human_SNP_ID_549903816 A-to-I Human chr14 + 31095491 31095491 31095491 TAGGCTGGAGTGCAGTGGTGTGATCATGCCTCACTACAGCCTGTACCTCCTGGGCTCAGGTGCTC TAGGCTGGAGTGCAGTGGTGTGATCATGCCTCGCTACAGCCTGTACCTCCTGGGCTCAGGTGCTC A G AP4S1 Ensembl:ENSG00000100478 Protein coding 3'UTR GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs1485973478 Functional Loss SNV dbSNP153 33..33 33 - - - 25536 RMVar_ID_25536 Human_SNP_ID_549903839 A-to-I Human chr14 + 31095604 31095604 31095604 TCCACCCAGCTAATTTTTGTATTTTGTTGTAGAGATAGGGTTTCACTATGTTGCCCAGACTGGTC TCCACCCAGCTAATTTTTGTATTTTGTTGTAGGGATAGGGTTTCACTATGTTGCCCAGACTGGTC A G AP4S1 Ensembl:ENSG00000100478 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1416327581 Functional Loss SNV dbSNP153 33..33 33 - - - 25537 RMVar_ID_25537 Human_SNP_ID_549903843 A-to-I Human chr14 + 31095608 31095608 31095608 CCCAGCTAATTTTTGTATTTTGTTGTAGAGATAGGGTTTCACTATGTTGCCCAGACTGGTCTCGA CCCAGCTAATTTTTGTATTTTGTTGTAGAGATGGGGTTTCACTATGTTGCCCAGACTGGTCTCGA A G AP4S1 Ensembl:ENSG00000100478 Protein coding 3'UTR GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;ASD brains,temporal_cortex;Bronchiolar epithelium,BEP2D cell line - 29129909,30559470,31158229 RNA-Seq:(High) rs1180785835 Functional Loss SNV dbSNP153 33..33 33 - - - 25538 RMVar_ID_25538 Human_SNP_ID_549903844 A-to-I Human chr14 + 31095619 31095619 31095619 TTTGTATTTTGTTGTAGAGATAGGGTTTCACTATGTTGCCCAGACTGGTCTCGAATTCCTGCAGT TTTGTATTTTGTTGTAGAGATAGGGTTTCACTGTGTTGCCCAGACTGGTCTCGAATTCCTGCAGT A G AP4S1 Ensembl:ENSG00000100478 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1375283664 Functional Loss SNV dbSNP153 33..33 33 - - - 25539 RMVar_ID_25539 Human_SNP_ID_549903901 A-to-I Human chr14 + 31095828 31095828 31095828 GAATGCAGCCAGGCATGGTGGCTTACGCCTATAATCCCAGCACTTTGGGACGCCAAGGTGGGTAG GAATGCAGCCAGGCATGGTGGCTTACGCCTATGATCCCAGCACTTTGGGACGCCAAGGTGGGTAG A G AP4S1 Ensembl:ENSG00000100478 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1430145895 Functional Loss SNV dbSNP153 33..33 33 - - - 25540 RMVar_ID_25540 Human_SNP_ID_549904410 A-to-I Human chr14 + 31097430 31097430 31097430 TTTTCCTTTAAATATAGAGACGGGGTCTCACTATGTTCCCCAGGCTGGTCTCAAACTCCTGGGCT TTTTCCTTTAAATATAGAGACGGGGTCTCACTGTGTTCCCCAGGCTGGTCTCAAACTCCTGGGCT A G AP4S1 Ensembl:ENSG00000100478 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167354999 Functional Loss SNV dbSNP153 33..33 33 - - - 25541 RMVar_ID_25541 Human_SNP_ID_549904918 A-to-I Human chr14 + 31099523 31099523 31099523 GTGATACACATCTGTAATCCCAGCTACTCCAGAAGCTGTGGTGGCAGGACTGCTTGAACCTAGGA GTGATACACATCTGTAATCCCAGCTACTCCAGTAGCTGTGGTGGCAGGACTGCTTGAACCTAGGA A T AP4S1 Ensembl:ENSG00000100478 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355856481 Functional Loss SNV dbSNP153 33..33 33 - - - 25542 RMVar_ID_25542 Human_SNP_ID_549905418 A-to-I Human chr14 - 31101576 31101576 31101576 GTTTGTCAGGCTGCTGTTGAACTCTTGACCTCAGATGATCCACCCGCCTCAGCCTCCCAAGGTGC GTTTGTCAGGCTGCTGTTGAACTCTTGACCTCGGATGATCCACCCGCCTCAGCCTCCCAAGGTGC T C HECTD1 Ensembl:ENSG00000092148 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965468696 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107177,RMVar_hsa_circ_165588,RMVar_hsa_circ_165587,RMVar_hsa_circ_117514,RMVar_hsa_circ_82327,RMVar_hsa_circ_83025,RMVar_hsa_circ_165591,RMVar_hsa_circ_165592,RMVar_hsa_circ_165590 25543 RMVar_ID_25543 Human_SNP_ID_549909506 A-to-I Human chr14 - 31118047 31118047 31118047 TGAGCCAAGATCACACCACTGCACTCCAGCCTAGGTGACAGAGTGAGACTCTGTCTCGAACAAAA TGAGCCAAGATCACACCACTGCACTCCAGCCTGGGTGACAGAGTGAGACTCTGTCTCGAACAAAA T C HECTD1 Ensembl:ENSG00000092148 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs138534292 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82327,RMVar_hsa_circ_165592,RMVar_hsa_circ_347937,RMVar_hsa_circ_358742,RMVar_hsa_circ_48009,RMVar_hsa_circ_307546,RMVar_hsa_circ_321639,RMVar_hsa_circ_37360,RMVar_hsa_circ_41522,RMVar_hsa_circ_70991,RMVar_hsa_circ_125440,RMVar_hsa_circ_107789,RMVar_hsa_circ_7152,RMVar_hsa_circ_165595,RMVar_hsa_circ_165596,RMVar_hsa_circ_165598,RMVar_hsa_circ_39891,RMVar_hsa_circ_267295,RMVar_hsa_circ_350210,RMVar_hsa_circ_165597,RMVar_hsa_circ_266804,RMVar_hsa_circ_345355,RMVar_hsa_circ_66263,RMVar_hsa_circ_280514,RMVar_hsa_circ_363619,RMVar_hsa_circ_165602,RMVar_hsa_circ_41895,RMVar_hsa_circ_27121,RMVar_hsa_circ_165603,RMVar_hsa_circ_305619,RMVar_hsa_circ_357073,RMVar_hsa_circ_378285,RMVar_hsa_circ_281698,RMVar_hsa_circ_272961,RMVar_hsa_circ_54663,RMVar_hsa_circ_90569,RMVar_hsa_circ_165605,RMVar_hsa_circ_165606,RMVar_hsa_circ_165604,RMVar_hsa_circ_365750,RMVar_hsa_circ_165607,RMVar_hsa_circ_374505,RMVar_hsa_circ_69930,RMVar_hsa_circ_118959,RMVar_hsa_circ_124169,RMVar_hsa_circ_165608,RMVar_hsa_circ_66079,RMVar_hsa_circ_109093,RMVar_hsa_circ_312088,RMVar_hsa_circ_165609,RMVar_hsa_circ_165610,RMVar_hsa_circ_343488,RMVar_hsa_circ_360595,RMVar_hsa_circ_288844,RMVar_hsa_circ_301727,RMVar_hsa_circ_287256,RMVar_hsa_circ_96373,RMVar_hsa_circ_105782,RMVar_hsa_circ_61626,RMVar_hsa_circ_165611,RMVar_hsa_circ_165613,RMVar_hsa_circ_165615,RMVar_hsa_circ_165616,RMVar_hsa_circ_165617,RMVar_hsa_circ_165614,RMVar_hsa_circ_165612 25544 RMVar_ID_25544 Human_SNP_ID_549909522 A-to-I Human chr14 - 31118144 31118144 31118144 AAAATTAGCCAGGCTTGGTGGTGCGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA AAAATTAGCCAGGCTTGGTGGTGCGCGCCTGTGATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA T C HECTD1 Ensembl:ENSG00000092148 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs932184895 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82327,RMVar_hsa_circ_165592,RMVar_hsa_circ_347937,RMVar_hsa_circ_358742,RMVar_hsa_circ_48009,RMVar_hsa_circ_307546,RMVar_hsa_circ_321639,RMVar_hsa_circ_37360,RMVar_hsa_circ_41522,RMVar_hsa_circ_70991,RMVar_hsa_circ_125440,RMVar_hsa_circ_107789,RMVar_hsa_circ_7152,RMVar_hsa_circ_165595,RMVar_hsa_circ_165596,RMVar_hsa_circ_165598,RMVar_hsa_circ_39891,RMVar_hsa_circ_267295,RMVar_hsa_circ_350210,RMVar_hsa_circ_165597,RMVar_hsa_circ_266804,RMVar_hsa_circ_345355,RMVar_hsa_circ_66263,RMVar_hsa_circ_280514,RMVar_hsa_circ_363619,RMVar_hsa_circ_165602,RMVar_hsa_circ_41895,RMVar_hsa_circ_27121,RMVar_hsa_circ_165603,RMVar_hsa_circ_305619,RMVar_hsa_circ_357073,RMVar_hsa_circ_378285,RMVar_hsa_circ_281698,RMVar_hsa_circ_272961,RMVar_hsa_circ_54663,RMVar_hsa_circ_90569,RMVar_hsa_circ_165605,RMVar_hsa_circ_165606,RMVar_hsa_circ_165604,RMVar_hsa_circ_365750,RMVar_hsa_circ_165607,RMVar_hsa_circ_374505,RMVar_hsa_circ_69930,RMVar_hsa_circ_118959,RMVar_hsa_circ_124169,RMVar_hsa_circ_165608,RMVar_hsa_circ_66079,RMVar_hsa_circ_109093,RMVar_hsa_circ_312088,RMVar_hsa_circ_165609,RMVar_hsa_circ_165610,RMVar_hsa_circ_343488,RMVar_hsa_circ_360595,RMVar_hsa_circ_288844,RMVar_hsa_circ_301727,RMVar_hsa_circ_287256,RMVar_hsa_circ_96373,RMVar_hsa_circ_105782,RMVar_hsa_circ_61626,RMVar_hsa_circ_165611,RMVar_hsa_circ_165613,RMVar_hsa_circ_165615,RMVar_hsa_circ_165616,RMVar_hsa_circ_165617,RMVar_hsa_circ_165614,RMVar_hsa_circ_165612 25545 RMVar_ID_25545 Human_SNP_ID_549914672 A-to-I Human chr14 - 31137268 31137268 31137268 AAAGTAGCCGGGCGTGGTGGCACGCACCTGTAATCCCAACTACTCAGGAGGCTGAGGTAGGAGAA AAAGTAGCCGGGCGTGGTGGCACGCACCTGTATTCCCAACTACTCAGGAGGCTGAGGTAGGAGAA T A HECTD1 Ensembl:ENSG00000092148 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1203893173 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48009,RMVar_hsa_circ_307546,RMVar_hsa_circ_33085,RMVar_hsa_circ_70991,RMVar_hsa_circ_7152,RMVar_hsa_circ_165598,RMVar_hsa_circ_267295,RMVar_hsa_circ_345355,RMVar_hsa_circ_27121,RMVar_hsa_circ_165603,RMVar_hsa_circ_305619,RMVar_hsa_circ_357073,RMVar_hsa_circ_378285,RMVar_hsa_circ_165604,RMVar_hsa_circ_374505,RMVar_hsa_circ_165608,RMVar_hsa_circ_312088,RMVar_hsa_circ_96373,RMVar_hsa_circ_105782,RMVar_hsa_circ_266577,RMVar_hsa_circ_165611,RMVar_hsa_circ_165613,RMVar_hsa_circ_165612,RMVar_hsa_circ_279221,RMVar_hsa_circ_165623,RMVar_hsa_circ_321990,RMVar_hsa_circ_346313,RMVar_hsa_circ_356676,RMVar_hsa_circ_373221,RMVar_hsa_circ_362617,RMVar_hsa_circ_371480,RMVar_hsa_circ_333146,RMVar_hsa_circ_337428,RMVar_hsa_circ_293574,RMVar_hsa_circ_306698,RMVar_hsa_circ_275050,RMVar_hsa_circ_277876,RMVar_hsa_circ_270426,RMVar_hsa_circ_102451,RMVar_hsa_circ_103098,RMVar_hsa_circ_49106,RMVar_hsa_circ_4371,RMVar_hsa_circ_165628,RMVar_hsa_circ_165632,RMVar_hsa_circ_165636,RMVar_hsa_circ_165634,RMVar_hsa_circ_165635,RMVar_hsa_circ_165633,RMVar_hsa_circ_165630,RMVar_hsa_circ_165631,RMVar_hsa_circ_165629,RMVar_hsa_circ_85428,RMVar_hsa_circ_165642,RMVar_hsa_circ_165626,RMVar_hsa_circ_165627,RMVar_hsa_circ_124798,RMVar_hsa_circ_369323,RMVar_hsa_circ_311550,RMVar_hsa_circ_311806,RMVar_hsa_circ_8378,RMVar_hsa_circ_46252,RMVar_hsa_circ_165649,RMVar_hsa_circ_165650,RMVar_hsa_circ_165648,RMVar_hsa_circ_165651,RMVar_hsa_circ_103405,RMVar_hsa_circ_335757,RMVar_hsa_circ_338235,RMVar_hsa_circ_315297,RMVar_hsa_circ_165652,RMVar_hsa_circ_165653,RMVar_hsa_circ_363735,RMVar_hsa_circ_378463,RMVar_hsa_circ_15673,RMVar_hsa_circ_165655,RMVar_hsa_circ_71719,RMVar_hsa_circ_122055,RMVar_hsa_circ_301259,RMVar_hsa_circ_325431,RMVar_hsa_circ_85479,RMVar_hsa_circ_32440,RMVar_hsa_circ_165654 25546 RMVar_ID_25546 Human_SNP_ID_549918942 A-to-I Human chr14 - 31153340 31153340 31153340 TTTGAGATGGAGTCTCGCTCTGTCGTGATCTCAGCTCACTGCTAGCTCTGCCTCCCGGATTCAAG TTTGAGATGGAGTCTCGCTCTGTCGTGATCTCGGCTCACTGCTAGCTCTGCCTCCCGGATTCAAG T C HECTD1 Ensembl:ENSG00000092148 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1461538383 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12460287 RMVar_hsa_circ_48009,RMVar_hsa_circ_307546,RMVar_hsa_circ_33085,RMVar_hsa_circ_165598,RMVar_hsa_circ_345355,RMVar_hsa_circ_165603,RMVar_hsa_circ_305619,RMVar_hsa_circ_378285,RMVar_hsa_circ_165604,RMVar_hsa_circ_374505,RMVar_hsa_circ_165608,RMVar_hsa_circ_312088,RMVar_hsa_circ_96373,RMVar_hsa_circ_105782,RMVar_hsa_circ_165611,RMVar_hsa_circ_165613,RMVar_hsa_circ_165612,RMVar_hsa_circ_279221,RMVar_hsa_circ_165623,RMVar_hsa_circ_321990,RMVar_hsa_circ_346313,RMVar_hsa_circ_356676,RMVar_hsa_circ_337428,RMVar_hsa_circ_293574,RMVar_hsa_circ_306698,RMVar_hsa_circ_275050,RMVar_hsa_circ_270426,RMVar_hsa_circ_102451,RMVar_hsa_circ_49106,RMVar_hsa_circ_165628,RMVar_hsa_circ_165632,RMVar_hsa_circ_165630,RMVar_hsa_circ_165631,RMVar_hsa_circ_165629,RMVar_hsa_circ_165642,RMVar_hsa_circ_165626,RMVar_hsa_circ_165627,RMVar_hsa_circ_124798,RMVar_hsa_circ_311550,RMVar_hsa_circ_8378,RMVar_hsa_circ_46252,RMVar_hsa_circ_165650,RMVar_hsa_circ_335757,RMVar_hsa_circ_363735,RMVar_hsa_circ_49041,RMVar_hsa_circ_165655,RMVar_hsa_circ_122055,RMVar_hsa_circ_85479,RMVar_hsa_circ_32440,RMVar_hsa_circ_28848,RMVar_hsa_circ_165654,RMVar_hsa_circ_313312,RMVar_hsa_circ_322100,RMVar_hsa_circ_165657,RMVar_hsa_circ_350623,RMVar_hsa_circ_354436,RMVar_hsa_circ_48081,RMVar_hsa_circ_302193,RMVar_hsa_circ_165660,RMVar_hsa_circ_165661,RMVar_hsa_circ_165659,RMVar_hsa_circ_288681,RMVar_hsa_circ_342444,RMVar_hsa_circ_68139,RMVar_hsa_circ_63730,RMVar_hsa_circ_74149,RMVar_hsa_circ_165663,RMVar_hsa_circ_26957,RMVar_hsa_circ_42810,RMVar_hsa_circ_25347,RMVar_hsa_circ_165664,RMVar_hsa_circ_361326,RMVar_hsa_circ_165662,RMVar_hsa_circ_269392,RMVar_hsa_circ_360324,RMVar_hsa_circ_359867,RMVar_hsa_circ_265865 25547 RMVar_ID_25547 Human_SNP_ID_549920202 A-to-I Human chr14 - 31157754 31157754 31157754 TTTTGTATTTTTAGTAGAGACGGGGTTTCTCCATGTTGGCCAAGCTAGTCTTGAACTCCTGACCT TTTTGTATTTTTAGTAGAGACGGGGTTTCTCCCTGTTGGCCAAGCTAGTCTTGAACTCCTGACCT T G HECTD1 Ensembl:ENSG00000092148 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1196081306 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48009,RMVar_hsa_circ_307546,RMVar_hsa_circ_33085,RMVar_hsa_circ_165598,RMVar_hsa_circ_345355,RMVar_hsa_circ_165603,RMVar_hsa_circ_305619,RMVar_hsa_circ_378285,RMVar_hsa_circ_165604,RMVar_hsa_circ_374505,RMVar_hsa_circ_165608,RMVar_hsa_circ_312088,RMVar_hsa_circ_96373,RMVar_hsa_circ_105782,RMVar_hsa_circ_165611,RMVar_hsa_circ_165613,RMVar_hsa_circ_165612,RMVar_hsa_circ_279221,RMVar_hsa_circ_165623,RMVar_hsa_circ_321990,RMVar_hsa_circ_346313,RMVar_hsa_circ_356676,RMVar_hsa_circ_337428,RMVar_hsa_circ_293574,RMVar_hsa_circ_306698,RMVar_hsa_circ_270426,RMVar_hsa_circ_49106,RMVar_hsa_circ_165628,RMVar_hsa_circ_165630,RMVar_hsa_circ_165629,RMVar_hsa_circ_165626,RMVar_hsa_circ_165627,RMVar_hsa_circ_311550,RMVar_hsa_circ_8378,RMVar_hsa_circ_46252,RMVar_hsa_circ_165650,RMVar_hsa_circ_335757,RMVar_hsa_circ_363735,RMVar_hsa_circ_49041,RMVar_hsa_circ_165655,RMVar_hsa_circ_122055,RMVar_hsa_circ_85479,RMVar_hsa_circ_32440,RMVar_hsa_circ_28848,RMVar_hsa_circ_165654,RMVar_hsa_circ_313312,RMVar_hsa_circ_322100,RMVar_hsa_circ_165657,RMVar_hsa_circ_354436,RMVar_hsa_circ_48081,RMVar_hsa_circ_302193,RMVar_hsa_circ_165660,RMVar_hsa_circ_165661,RMVar_hsa_circ_165659,RMVar_hsa_circ_288681,RMVar_hsa_circ_342444,RMVar_hsa_circ_68139,RMVar_hsa_circ_63730,RMVar_hsa_circ_165663,RMVar_hsa_circ_26957,RMVar_hsa_circ_42810,RMVar_hsa_circ_361326,RMVar_hsa_circ_165662,RMVar_hsa_circ_269392,RMVar_hsa_circ_360324,RMVar_hsa_circ_359867,RMVar_hsa_circ_265865,RMVar_hsa_circ_165668,RMVar_hsa_circ_76899,RMVar_hsa_circ_307757,RMVar_hsa_circ_323419,RMVar_hsa_circ_369009,RMVar_hsa_circ_308514,RMVar_hsa_circ_119359,RMVar_hsa_circ_165670,RMVar_hsa_circ_70459,RMVar_hsa_circ_165671,RMVar_hsa_circ_165669,RMVar_hsa_circ_61550 25548 RMVar_ID_25548 Human_SNP_ID_549920508 A-to-I Human chr14 - 31158857 31158857 31158857 CTGCTGCAACCTCTGCCTCTAGGGTTCAAGCAATTCTTCTGTCTCAGCCTCCTGAGTAGCTGGGA CTGCTGCAACCTCTGCCTCTAGGGTTCAAGCAGTTCTTCTGTCTCAGCCTCCTGAGTAGCTGGGA T C HECTD1 Ensembl:ENSG00000092148 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs932227971 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48009,RMVar_hsa_circ_307546,RMVar_hsa_circ_33085,RMVar_hsa_circ_165598,RMVar_hsa_circ_345355,RMVar_hsa_circ_165603,RMVar_hsa_circ_305619,RMVar_hsa_circ_378285,RMVar_hsa_circ_165604,RMVar_hsa_circ_374505,RMVar_hsa_circ_165608,RMVar_hsa_circ_312088,RMVar_hsa_circ_96373,RMVar_hsa_circ_105782,RMVar_hsa_circ_165611,RMVar_hsa_circ_165613,RMVar_hsa_circ_165612,RMVar_hsa_circ_279221,RMVar_hsa_circ_165623,RMVar_hsa_circ_321990,RMVar_hsa_circ_346313,RMVar_hsa_circ_356676,RMVar_hsa_circ_337428,RMVar_hsa_circ_293574,RMVar_hsa_circ_306698,RMVar_hsa_circ_270426,RMVar_hsa_circ_49106,RMVar_hsa_circ_165628,RMVar_hsa_circ_165630,RMVar_hsa_circ_165629,RMVar_hsa_circ_165626,RMVar_hsa_circ_165627,RMVar_hsa_circ_311550,RMVar_hsa_circ_8378,RMVar_hsa_circ_46252,RMVar_hsa_circ_165650,RMVar_hsa_circ_335757,RMVar_hsa_circ_363735,RMVar_hsa_circ_49041,RMVar_hsa_circ_165655,RMVar_hsa_circ_122055,RMVar_hsa_circ_85479,RMVar_hsa_circ_32440,RMVar_hsa_circ_28848,RMVar_hsa_circ_165654,RMVar_hsa_circ_313312,RMVar_hsa_circ_322100,RMVar_hsa_circ_165657,RMVar_hsa_circ_354436,RMVar_hsa_circ_48081,RMVar_hsa_circ_302193,RMVar_hsa_circ_165660,RMVar_hsa_circ_165661,RMVar_hsa_circ_165659,RMVar_hsa_circ_288681,RMVar_hsa_circ_342444,RMVar_hsa_circ_68139,RMVar_hsa_circ_63730,RMVar_hsa_circ_165663,RMVar_hsa_circ_26957,RMVar_hsa_circ_42810,RMVar_hsa_circ_361326,RMVar_hsa_circ_165662,RMVar_hsa_circ_269392,RMVar_hsa_circ_360324,RMVar_hsa_circ_359867,RMVar_hsa_circ_265865,RMVar_hsa_circ_165668,RMVar_hsa_circ_76899,RMVar_hsa_circ_307757,RMVar_hsa_circ_323419,RMVar_hsa_circ_369009,RMVar_hsa_circ_308514,RMVar_hsa_circ_119359,RMVar_hsa_circ_165670,RMVar_hsa_circ_70459,RMVar_hsa_circ_165671,RMVar_hsa_circ_165669,RMVar_hsa_circ_61550 25549 RMVar_ID_25549 Human_SNP_ID_549920510 A-to-I Human chr14 - 31158861 31158861 31158861 TGGCCTGCTGCAACCTCTGCCTCTAGGGTTCAAGCAATTCTTCTGTCTCAGCCTCCTGAGTAGCT TGGCCTGCTGCAACCTCTGCCTCTAGGGTTCAGGCAATTCTTCTGTCTCAGCCTCCTGAGTAGCT T C HECTD1 Ensembl:ENSG00000092148 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs932530480 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48009,RMVar_hsa_circ_307546,RMVar_hsa_circ_33085,RMVar_hsa_circ_165598,RMVar_hsa_circ_345355,RMVar_hsa_circ_165603,RMVar_hsa_circ_305619,RMVar_hsa_circ_378285,RMVar_hsa_circ_165604,RMVar_hsa_circ_374505,RMVar_hsa_circ_165608,RMVar_hsa_circ_312088,RMVar_hsa_circ_96373,RMVar_hsa_circ_105782,RMVar_hsa_circ_165611,RMVar_hsa_circ_165613,RMVar_hsa_circ_165612,RMVar_hsa_circ_279221,RMVar_hsa_circ_165623,RMVar_hsa_circ_321990,RMVar_hsa_circ_346313,RMVar_hsa_circ_356676,RMVar_hsa_circ_337428,RMVar_hsa_circ_293574,RMVar_hsa_circ_306698,RMVar_hsa_circ_270426,RMVar_hsa_circ_49106,RMVar_hsa_circ_165628,RMVar_hsa_circ_165630,RMVar_hsa_circ_165629,RMVar_hsa_circ_165626,RMVar_hsa_circ_165627,RMVar_hsa_circ_311550,RMVar_hsa_circ_8378,RMVar_hsa_circ_46252,RMVar_hsa_circ_165650,RMVar_hsa_circ_335757,RMVar_hsa_circ_363735,RMVar_hsa_circ_49041,RMVar_hsa_circ_165655,RMVar_hsa_circ_122055,RMVar_hsa_circ_85479,RMVar_hsa_circ_32440,RMVar_hsa_circ_28848,RMVar_hsa_circ_165654,RMVar_hsa_circ_313312,RMVar_hsa_circ_322100,RMVar_hsa_circ_165657,RMVar_hsa_circ_354436,RMVar_hsa_circ_48081,RMVar_hsa_circ_302193,RMVar_hsa_circ_165660,RMVar_hsa_circ_165661,RMVar_hsa_circ_165659,RMVar_hsa_circ_288681,RMVar_hsa_circ_342444,RMVar_hsa_circ_68139,RMVar_hsa_circ_63730,RMVar_hsa_circ_165663,RMVar_hsa_circ_26957,RMVar_hsa_circ_42810,RMVar_hsa_circ_361326,RMVar_hsa_circ_165662,RMVar_hsa_circ_269392,RMVar_hsa_circ_360324,RMVar_hsa_circ_359867,RMVar_hsa_circ_265865,RMVar_hsa_circ_165668,RMVar_hsa_circ_76899,RMVar_hsa_circ_307757,RMVar_hsa_circ_323419,RMVar_hsa_circ_369009,RMVar_hsa_circ_308514,RMVar_hsa_circ_119359,RMVar_hsa_circ_165670,RMVar_hsa_circ_70459,RMVar_hsa_circ_165671,RMVar_hsa_circ_165669,RMVar_hsa_circ_61550 25550 RMVar_ID_25550 Human_SNP_ID_549920671 A-to-I Human chr14 - 31159478 31159478 31159478 AAAATTAGCTGGGTGTGGTGGTGCACACCTGTAATCACAACTACTCTGGAGACTGAGACAGGAGA AAAATTAGCTGGGTGTGGTGGTGCACACCTGTGATCACAACTACTCTGGAGACTGAGACAGGAGA T C HECTD1 Ensembl:ENSG00000092148 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1247210723 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48009,RMVar_hsa_circ_307546,RMVar_hsa_circ_33085,RMVar_hsa_circ_165598,RMVar_hsa_circ_345355,RMVar_hsa_circ_165603,RMVar_hsa_circ_305619,RMVar_hsa_circ_378285,RMVar_hsa_circ_165604,RMVar_hsa_circ_374505,RMVar_hsa_circ_165608,RMVar_hsa_circ_312088,RMVar_hsa_circ_96373,RMVar_hsa_circ_105782,RMVar_hsa_circ_165611,RMVar_hsa_circ_165613,RMVar_hsa_circ_165612,RMVar_hsa_circ_279221,RMVar_hsa_circ_165623,RMVar_hsa_circ_321990,RMVar_hsa_circ_346313,RMVar_hsa_circ_356676,RMVar_hsa_circ_337428,RMVar_hsa_circ_293574,RMVar_hsa_circ_306698,RMVar_hsa_circ_270426,RMVar_hsa_circ_49106,RMVar_hsa_circ_165628,RMVar_hsa_circ_165630,RMVar_hsa_circ_165629,RMVar_hsa_circ_165626,RMVar_hsa_circ_165627,RMVar_hsa_circ_311550,RMVar_hsa_circ_8378,RMVar_hsa_circ_46252,RMVar_hsa_circ_165650,RMVar_hsa_circ_335757,RMVar_hsa_circ_363735,RMVar_hsa_circ_49041,RMVar_hsa_circ_165655,RMVar_hsa_circ_122055,RMVar_hsa_circ_85479,RMVar_hsa_circ_32440,RMVar_hsa_circ_28848,RMVar_hsa_circ_165654,RMVar_hsa_circ_313312,RMVar_hsa_circ_322100,RMVar_hsa_circ_165657,RMVar_hsa_circ_354436,RMVar_hsa_circ_48081,RMVar_hsa_circ_302193,RMVar_hsa_circ_165660,RMVar_hsa_circ_165661,RMVar_hsa_circ_165659,RMVar_hsa_circ_288681,RMVar_hsa_circ_342444,RMVar_hsa_circ_68139,RMVar_hsa_circ_63730,RMVar_hsa_circ_165663,RMVar_hsa_circ_26957,RMVar_hsa_circ_42810,RMVar_hsa_circ_361326,RMVar_hsa_circ_165662,RMVar_hsa_circ_269392,RMVar_hsa_circ_360324,RMVar_hsa_circ_359867,RMVar_hsa_circ_265865,RMVar_hsa_circ_165668,RMVar_hsa_circ_76899,RMVar_hsa_circ_307757,RMVar_hsa_circ_323419,RMVar_hsa_circ_369009,RMVar_hsa_circ_308514,RMVar_hsa_circ_119359,RMVar_hsa_circ_165670,RMVar_hsa_circ_70459,RMVar_hsa_circ_165671,RMVar_hsa_circ_165669,RMVar_hsa_circ_61550 25551 RMVar_ID_25551 Human_SNP_ID_549921166 A-to-I Human chr14 - 31161444 31161444 31161444 CCTCAGCCTCTTGAGTAGCTAGAACTGCAGGCACACACCACCAGGTCCAGCTAATTTTTATTTTT CCTCAGCCTCTTGAGTAGCTAGAACTGCAGGCGCACACCACCAGGTCCAGCTAATTTTTATTTTT T C HECTD1 Ensembl:ENSG00000092148 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs917976247 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48009,RMVar_hsa_circ_307546,RMVar_hsa_circ_33085,RMVar_hsa_circ_165598,RMVar_hsa_circ_345355,RMVar_hsa_circ_165603,RMVar_hsa_circ_305619,RMVar_hsa_circ_378285,RMVar_hsa_circ_165604,RMVar_hsa_circ_374505,RMVar_hsa_circ_165608,RMVar_hsa_circ_312088,RMVar_hsa_circ_96373,RMVar_hsa_circ_105782,RMVar_hsa_circ_165611,RMVar_hsa_circ_165613,RMVar_hsa_circ_165612,RMVar_hsa_circ_279221,RMVar_hsa_circ_165623,RMVar_hsa_circ_321990,RMVar_hsa_circ_346313,RMVar_hsa_circ_356676,RMVar_hsa_circ_337428,RMVar_hsa_circ_293574,RMVar_hsa_circ_306698,RMVar_hsa_circ_270426,RMVar_hsa_circ_49106,RMVar_hsa_circ_165628,RMVar_hsa_circ_165630,RMVar_hsa_circ_165629,RMVar_hsa_circ_165626,RMVar_hsa_circ_165627,RMVar_hsa_circ_311550,RMVar_hsa_circ_8378,RMVar_hsa_circ_46252,RMVar_hsa_circ_165650,RMVar_hsa_circ_335757,RMVar_hsa_circ_363735,RMVar_hsa_circ_49041,RMVar_hsa_circ_165655,RMVar_hsa_circ_122055,RMVar_hsa_circ_85479,RMVar_hsa_circ_32440,RMVar_hsa_circ_28848,RMVar_hsa_circ_165654,RMVar_hsa_circ_313312,RMVar_hsa_circ_322100,RMVar_hsa_circ_165657,RMVar_hsa_circ_354436,RMVar_hsa_circ_48081,RMVar_hsa_circ_302193,RMVar_hsa_circ_165660,RMVar_hsa_circ_165661,RMVar_hsa_circ_165659,RMVar_hsa_circ_288681,RMVar_hsa_circ_342444,RMVar_hsa_circ_68139,RMVar_hsa_circ_63730,RMVar_hsa_circ_165663,RMVar_hsa_circ_26957,RMVar_hsa_circ_42810,RMVar_hsa_circ_361326,RMVar_hsa_circ_165662,RMVar_hsa_circ_269392,RMVar_hsa_circ_360324,RMVar_hsa_circ_359867,RMVar_hsa_circ_265865,RMVar_hsa_circ_165668,RMVar_hsa_circ_76899,RMVar_hsa_circ_307757,RMVar_hsa_circ_323419,RMVar_hsa_circ_369009,RMVar_hsa_circ_308514,RMVar_hsa_circ_119359,RMVar_hsa_circ_165670,RMVar_hsa_circ_70459,RMVar_hsa_circ_165671,RMVar_hsa_circ_165669,RMVar_hsa_circ_61550 25552 RMVar_ID_25552 Human_SNP_ID_549922417 A-to-I Human chr14 - 31166002 31166002 31166002 GTCTCTATGAAAAATAAAAAAATTAGCTGGGTATGGTAGCACTTGGCTGTAGTCCCAGCTACTCG GTCTCTATGAAAAATAAAAAAATTAGCTGGGTGTGGTAGCACTTGGCTGTAGTCCCAGCTACTCG T C HECTD1 Ensembl:ENSG00000092148 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs972166278 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48009,RMVar_hsa_circ_307546,RMVar_hsa_circ_33085,RMVar_hsa_circ_165598,RMVar_hsa_circ_345355,RMVar_hsa_circ_165603,RMVar_hsa_circ_305619,RMVar_hsa_circ_378285,RMVar_hsa_circ_165604,RMVar_hsa_circ_374505,RMVar_hsa_circ_165608,RMVar_hsa_circ_312088,RMVar_hsa_circ_96373,RMVar_hsa_circ_105782,RMVar_hsa_circ_165611,RMVar_hsa_circ_165613,RMVar_hsa_circ_165612,RMVar_hsa_circ_279221,RMVar_hsa_circ_165623,RMVar_hsa_circ_321990,RMVar_hsa_circ_346313,RMVar_hsa_circ_356676,RMVar_hsa_circ_337428,RMVar_hsa_circ_293574,RMVar_hsa_circ_306698,RMVar_hsa_circ_270426,RMVar_hsa_circ_49106,RMVar_hsa_circ_165628,RMVar_hsa_circ_165629,RMVar_hsa_circ_165626,RMVar_hsa_circ_165627,RMVar_hsa_circ_311550,RMVar_hsa_circ_8378,RMVar_hsa_circ_46252,RMVar_hsa_circ_165650,RMVar_hsa_circ_335757,RMVar_hsa_circ_363735,RMVar_hsa_circ_49041,RMVar_hsa_circ_165655,RMVar_hsa_circ_122055,RMVar_hsa_circ_85479,RMVar_hsa_circ_32440,RMVar_hsa_circ_28848,RMVar_hsa_circ_165654,RMVar_hsa_circ_313312,RMVar_hsa_circ_322100,RMVar_hsa_circ_165657,RMVar_hsa_circ_354436,RMVar_hsa_circ_48081,RMVar_hsa_circ_302193,RMVar_hsa_circ_165660,RMVar_hsa_circ_165661,RMVar_hsa_circ_165659,RMVar_hsa_circ_288681,RMVar_hsa_circ_342444,RMVar_hsa_circ_68139,RMVar_hsa_circ_63730,RMVar_hsa_circ_165663,RMVar_hsa_circ_26957,RMVar_hsa_circ_42810,RMVar_hsa_circ_361326,RMVar_hsa_circ_165662,RMVar_hsa_circ_269392,RMVar_hsa_circ_360324,RMVar_hsa_circ_359867,RMVar_hsa_circ_265865,RMVar_hsa_circ_165668,RMVar_hsa_circ_76899,RMVar_hsa_circ_307757,RMVar_hsa_circ_323419,RMVar_hsa_circ_369009,RMVar_hsa_circ_308514,RMVar_hsa_circ_119359,RMVar_hsa_circ_165670,RMVar_hsa_circ_70459,RMVar_hsa_circ_165671,RMVar_hsa_circ_165669,RMVar_hsa_circ_61550 25553 RMVar_ID_25553 Human_SNP_ID_549929972 A-to-I Human chr14 - 31195686 31195686 31195686 GAAACCCCATCTCTACTAAAAATACAAAAATTAGCAGAGGTCTGGTGGCATGCGCCTGTAATCTC GAAACCCCATCTCTACTAAAAATACAAAAATTCGCAGAGGTCTGGTGGCATGCGCCTGTAATCTC T G HECTD1 Ensembl:ENSG00000092148 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404381407 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5947,RMVar_hsa_circ_105782,RMVar_hsa_circ_165611,RMVar_hsa_circ_8378,RMVar_hsa_circ_63730,RMVar_hsa_circ_119359,RMVar_hsa_circ_165671,RMVar_hsa_circ_165676 25554 RMVar_ID_25554 Human_SNP_ID_549930107 A-to-I Human chr14 - 31196181 31196179 31196181 GAAGAAACCCCCTCCCTACTAAAAATAGAAAAATTAGCAGGGTGTGGTGGCACATTCCTGTAATC GAAGAAACCCCCTCCCTACTAAAAATAGAAAA__TAGCAGGGTGTGGTGGCACATTCCTGTAATC AAT A HECTD1 Ensembl:ENSG00000092148 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1295175479 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_5947,RMVar_hsa_circ_105782,RMVar_hsa_circ_165611,RMVar_hsa_circ_8378,RMVar_hsa_circ_63730,RMVar_hsa_circ_119359,RMVar_hsa_circ_165671,RMVar_hsa_circ_165676 25555 RMVar_ID_25555 Human_SNP_ID_549930214 A-to-I Human chr14 - 31196668 31196668 31196668 CTCACTGTAACCTCTGCCTCCCGGGTTCAAGCAATGCTTCTGCCTTAGCCTTCTGAGTAGCTGGG CTCACTGTAACCTCTGCCTCCCGGGTTCAAGCGATGCTTCTGCCTTAGCCTTCTGAGTAGCTGGG T C HECTD1 Ensembl:ENSG00000092148 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1466097919 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5947,RMVar_hsa_circ_105782,RMVar_hsa_circ_165611,RMVar_hsa_circ_8378,RMVar_hsa_circ_63730,RMVar_hsa_circ_119359,RMVar_hsa_circ_165671,RMVar_hsa_circ_165676 25556 RMVar_ID_25556 Human_SNP_ID_549931191 A-to-I Human chr14 - 31200444 31200444 31200444 ACAAGGTCTCACTAGGTTCCCCAGGCTGATCTAGAACTCCTGAGCTTAAGTGATCCTCCCGCCTT ACAAGGTCTCACTAGGTTCCCCAGGCTGATCTGGAACTCCTGAGCTTAAGTGATCCTCCCGCCTT T C HECTD1 Ensembl:ENSG00000092148 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs865810380 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12315067,Human_RBP_ID_25093783 RMVar_hsa_circ_5947,RMVar_hsa_circ_105782,RMVar_hsa_circ_165611,RMVar_hsa_circ_8378,RMVar_hsa_circ_63730,RMVar_hsa_circ_119359,RMVar_hsa_circ_165671,RMVar_hsa_circ_165676 25557 RMVar_ID_25557 Human_SNP_ID_549931192 A-to-I Human chr14 - 31200444 31200444 31200444 ACAAGGTCTCACTAGGTTCCCCAGGCTGATCTAGAACTCCTGAGCTTAAGTGATCCTCCCGCCTT ACAAGGTCTCACTAGGTTCCCCAGGCTGATCTCGAACTCCTGAGCTTAAGTGATCCTCCCGCCTT T G HECTD1 Ensembl:ENSG00000092148 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs865810380 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12315067,Human_RBP_ID_25093783 RMVar_hsa_circ_5947,RMVar_hsa_circ_105782,RMVar_hsa_circ_165611,RMVar_hsa_circ_8378,RMVar_hsa_circ_63730,RMVar_hsa_circ_119359,RMVar_hsa_circ_165671,RMVar_hsa_circ_165676 25558 RMVar_ID_25558 Human_SNP_ID_549960432 A-to-I Human chr14 - 31312841 31312841 31312841 CAGGCTGGAGTGCCATGGTGCAATTTTGGCTCACTGCAACCTCTGCCTCCTGGGCTCAGGCGATC CAGGCTGGAGTGCCATGGTGCAATTTTGGCTCGCTGCAACCTCTGCCTCCTGGGCTCAGGCGATC T C HEATR5A Ensembl:ENSG00000129493 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs943259388 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44428,RMVar_hsa_circ_97381,RMVar_hsa_circ_93048,RMVar_hsa_circ_86159,RMVar_hsa_circ_119850,RMVar_hsa_circ_114924,RMVar_hsa_circ_95747,RMVar_hsa_circ_109949,RMVar_hsa_circ_165678,RMVar_hsa_circ_165680,RMVar_hsa_circ_165681,RMVar_hsa_circ_165679,RMVar_hsa_circ_165683,RMVar_hsa_circ_165684,RMVar_hsa_circ_368289,RMVar_hsa_circ_278379,RMVar_hsa_circ_327225,RMVar_hsa_circ_353324,RMVar_hsa_circ_373391,RMVar_hsa_circ_343730,RMVar_hsa_circ_336399,RMVar_hsa_circ_122985,RMVar_hsa_circ_276791,RMVar_hsa_circ_115772,RMVar_hsa_circ_116723,RMVar_hsa_circ_99941,RMVar_hsa_circ_165686,RMVar_hsa_circ_165690,RMVar_hsa_circ_58866,RMVar_hsa_circ_63980,RMVar_hsa_circ_165692,RMVar_hsa_circ_165693,RMVar_hsa_circ_165691,RMVar_hsa_circ_165688,RMVar_hsa_circ_165689,RMVar_hsa_circ_165687,RMVar_hsa_circ_78668,RMVar_hsa_circ_375049,RMVar_hsa_circ_109287,RMVar_hsa_circ_39964,RMVar_hsa_circ_165696,RMVar_hsa_circ_165698,RMVar_hsa_circ_20391,RMVar_hsa_circ_165697,RMVar_hsa_circ_340966,RMVar_hsa_circ_366255,RMVar_hsa_circ_342812,RMVar_hsa_circ_68445,RMVar_hsa_circ_90560,RMVar_hsa_circ_54292,RMVar_hsa_circ_332474,RMVar_hsa_circ_165701,RMVar_hsa_circ_165702,RMVar_hsa_circ_165703,RMVar_hsa_circ_355329,RMVar_hsa_circ_372873,RMVar_hsa_circ_353830,RMVar_hsa_circ_47548,RMVar_hsa_circ_323505,RMVar_hsa_circ_46913,RMVar_hsa_circ_118407,RMVar_hsa_circ_354951,RMVar_hsa_circ_165705,RMVar_hsa_circ_165706,RMVar_hsa_circ_165707,RMVar_hsa_circ_165704,RMVar_hsa_circ_374498,RMVar_hsa_circ_268993,RMVar_hsa_circ_344767,RMVar_hsa_circ_265432,RMVar_hsa_circ_110425,RMVar_hsa_circ_113365,RMVar_hsa_circ_46289,RMVar_hsa_circ_165709,RMVar_hsa_circ_165711,RMVar_hsa_circ_165713,RMVar_hsa_circ_165714,RMVar_hsa_circ_165712,RMVar_hsa_circ_165710,RMVar_hsa_circ_165708 25559 RMVar_ID_25559 Human_SNP_ID_549960970 A-to-I Human chr14 - 31315090 31315090 31315090 CAGCTCACTGCAGCCTCCACCTCCCAGTTTCAAGTGATTCTCGTGTCTCAACCTCCCAAGTAGCT CAGCTCACTGCAGCCTCCACCTCCCAGTTTCAGGTGATTCTCGTGTCTCAACCTCCCAAGTAGCT T C HEATR5A Ensembl:ENSG00000129493 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs551287001 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44428,RMVar_hsa_circ_97381,RMVar_hsa_circ_93048,RMVar_hsa_circ_86159,RMVar_hsa_circ_119850,RMVar_hsa_circ_114924,RMVar_hsa_circ_95747,RMVar_hsa_circ_109949,RMVar_hsa_circ_165678,RMVar_hsa_circ_165680,RMVar_hsa_circ_165681,RMVar_hsa_circ_165679,RMVar_hsa_circ_165683,RMVar_hsa_circ_165684,RMVar_hsa_circ_368289,RMVar_hsa_circ_278379,RMVar_hsa_circ_327225,RMVar_hsa_circ_353324,RMVar_hsa_circ_373391,RMVar_hsa_circ_343730,RMVar_hsa_circ_336399,RMVar_hsa_circ_122985,RMVar_hsa_circ_276791,RMVar_hsa_circ_115772,RMVar_hsa_circ_116723,RMVar_hsa_circ_99941,RMVar_hsa_circ_165686,RMVar_hsa_circ_165690,RMVar_hsa_circ_58866,RMVar_hsa_circ_63980,RMVar_hsa_circ_165692,RMVar_hsa_circ_165693,RMVar_hsa_circ_165691,RMVar_hsa_circ_165688,RMVar_hsa_circ_165689,RMVar_hsa_circ_165687,RMVar_hsa_circ_78668,RMVar_hsa_circ_375049,RMVar_hsa_circ_109287,RMVar_hsa_circ_39964,RMVar_hsa_circ_165696,RMVar_hsa_circ_165698,RMVar_hsa_circ_20391,RMVar_hsa_circ_165697,RMVar_hsa_circ_340966,RMVar_hsa_circ_366255,RMVar_hsa_circ_342812,RMVar_hsa_circ_68445,RMVar_hsa_circ_90560,RMVar_hsa_circ_54292,RMVar_hsa_circ_7643,RMVar_hsa_circ_332474,RMVar_hsa_circ_165701,RMVar_hsa_circ_165702,RMVar_hsa_circ_165703,RMVar_hsa_circ_355329,RMVar_hsa_circ_372873,RMVar_hsa_circ_353830,RMVar_hsa_circ_47548,RMVar_hsa_circ_323505,RMVar_hsa_circ_46913,RMVar_hsa_circ_118407,RMVar_hsa_circ_354951,RMVar_hsa_circ_165705,RMVar_hsa_circ_165706,RMVar_hsa_circ_165707,RMVar_hsa_circ_165704,RMVar_hsa_circ_374498,RMVar_hsa_circ_268993,RMVar_hsa_circ_344767,RMVar_hsa_circ_265432,RMVar_hsa_circ_110425,RMVar_hsa_circ_113365,RMVar_hsa_circ_46289,RMVar_hsa_circ_113638,RMVar_hsa_circ_165709,RMVar_hsa_circ_165711,RMVar_hsa_circ_165713,RMVar_hsa_circ_165714,RMVar_hsa_circ_165712,RMVar_hsa_circ_165710,RMVar_hsa_circ_339111,RMVar_hsa_circ_370214,RMVar_hsa_circ_165708,RMVar_hsa_circ_376105,RMVar_hsa_circ_353269,RMVar_hsa_circ_286646,RMVar_hsa_circ_54418,RMVar_hsa_circ_94685,RMVar_hsa_circ_50106,RMVar_hsa_circ_165716,RMVar_hsa_circ_165718,RMVar_hsa_circ_165719,RMVar_hsa_circ_165720,RMVar_hsa_circ_165717,RMVar_hsa_circ_165715 25560 RMVar_ID_25560 Human_SNP_ID_549961373 A-to-I Human chr14 - 31316848 31316848 31316848 TCCTTTCTCTATAAAAAAATAAAAAATTAGCCAGATGTGGTGGTATGTGCCTGTGGCCCTGTCTA TCCTTTCTCTATAAAAAAATAAAAAATTAGCCGGATGTGGTGGTATGTGCCTGTGGCCCTGTCTA T C HEATR5A Ensembl:ENSG00000129493 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1000692599 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44428,RMVar_hsa_circ_97381,RMVar_hsa_circ_93048,RMVar_hsa_circ_86159,RMVar_hsa_circ_119850,RMVar_hsa_circ_95747,RMVar_hsa_circ_165680,RMVar_hsa_circ_165681,RMVar_hsa_circ_165679,RMVar_hsa_circ_165684,RMVar_hsa_circ_368289,RMVar_hsa_circ_278379,RMVar_hsa_circ_327225,RMVar_hsa_circ_353324,RMVar_hsa_circ_373391,RMVar_hsa_circ_343730,RMVar_hsa_circ_336399,RMVar_hsa_circ_122985,RMVar_hsa_circ_276791,RMVar_hsa_circ_115772,RMVar_hsa_circ_116723,RMVar_hsa_circ_99941,RMVar_hsa_circ_165686,RMVar_hsa_circ_165690,RMVar_hsa_circ_58866,RMVar_hsa_circ_165692,RMVar_hsa_circ_165693,RMVar_hsa_circ_165691,RMVar_hsa_circ_165688,RMVar_hsa_circ_165689,RMVar_hsa_circ_165687,RMVar_hsa_circ_78668,RMVar_hsa_circ_375049,RMVar_hsa_circ_109287,RMVar_hsa_circ_165696,RMVar_hsa_circ_165698,RMVar_hsa_circ_20391,RMVar_hsa_circ_165697,RMVar_hsa_circ_366255,RMVar_hsa_circ_342812,RMVar_hsa_circ_68445,RMVar_hsa_circ_90560,RMVar_hsa_circ_54292,RMVar_hsa_circ_7643,RMVar_hsa_circ_165702,RMVar_hsa_circ_165703,RMVar_hsa_circ_355329,RMVar_hsa_circ_372873,RMVar_hsa_circ_353830,RMVar_hsa_circ_47548,RMVar_hsa_circ_323505,RMVar_hsa_circ_46913,RMVar_hsa_circ_118407,RMVar_hsa_circ_165705,RMVar_hsa_circ_165706,RMVar_hsa_circ_165704,RMVar_hsa_circ_374498,RMVar_hsa_circ_268993,RMVar_hsa_circ_344767,RMVar_hsa_circ_265432,RMVar_hsa_circ_110425,RMVar_hsa_circ_113365,RMVar_hsa_circ_46289,RMVar_hsa_circ_113638,RMVar_hsa_circ_165709,RMVar_hsa_circ_165711,RMVar_hsa_circ_165713,RMVar_hsa_circ_165714,RMVar_hsa_circ_165712,RMVar_hsa_circ_165710,RMVar_hsa_circ_339111,RMVar_hsa_circ_376105,RMVar_hsa_circ_353269,RMVar_hsa_circ_286646,RMVar_hsa_circ_54418,RMVar_hsa_circ_94685,RMVar_hsa_circ_50106,RMVar_hsa_circ_47081,RMVar_hsa_circ_165716,RMVar_hsa_circ_165718,RMVar_hsa_circ_165719,RMVar_hsa_circ_165717,RMVar_hsa_circ_336134,RMVar_hsa_circ_357854,RMVar_hsa_circ_165715,RMVar_hsa_circ_361029,RMVar_hsa_circ_337444,RMVar_hsa_circ_102824,RMVar_hsa_circ_307917,RMVar_hsa_circ_69700,RMVar_hsa_circ_165721,RMVar_hsa_circ_45136,RMVar_hsa_circ_165722 25561 RMVar_ID_25561 Human_SNP_ID_549961375 A-to-I Human chr14 - 31316852 31316852 31316852 GAGATCCTTTCTCTATAAAAAAATAAAAAATTAGCCAGATGTGGTGGTATGTGCCTGTGGCCCTG GAGATCCTTTCTCTATAAAAAAATAAAAAATTGGCCAGATGTGGTGGTATGTGCCTGTGGCCCTG T C HEATR5A Ensembl:ENSG00000129493 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1438242049 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44428,RMVar_hsa_circ_97381,RMVar_hsa_circ_93048,RMVar_hsa_circ_86159,RMVar_hsa_circ_119850,RMVar_hsa_circ_95747,RMVar_hsa_circ_165680,RMVar_hsa_circ_165681,RMVar_hsa_circ_165679,RMVar_hsa_circ_165684,RMVar_hsa_circ_368289,RMVar_hsa_circ_278379,RMVar_hsa_circ_327225,RMVar_hsa_circ_353324,RMVar_hsa_circ_373391,RMVar_hsa_circ_343730,RMVar_hsa_circ_336399,RMVar_hsa_circ_122985,RMVar_hsa_circ_276791,RMVar_hsa_circ_115772,RMVar_hsa_circ_116723,RMVar_hsa_circ_99941,RMVar_hsa_circ_165686,RMVar_hsa_circ_165690,RMVar_hsa_circ_58866,RMVar_hsa_circ_165692,RMVar_hsa_circ_165693,RMVar_hsa_circ_165691,RMVar_hsa_circ_165688,RMVar_hsa_circ_165689,RMVar_hsa_circ_165687,RMVar_hsa_circ_78668,RMVar_hsa_circ_375049,RMVar_hsa_circ_109287,RMVar_hsa_circ_165696,RMVar_hsa_circ_165698,RMVar_hsa_circ_20391,RMVar_hsa_circ_165697,RMVar_hsa_circ_366255,RMVar_hsa_circ_342812,RMVar_hsa_circ_68445,RMVar_hsa_circ_90560,RMVar_hsa_circ_54292,RMVar_hsa_circ_7643,RMVar_hsa_circ_165702,RMVar_hsa_circ_165703,RMVar_hsa_circ_355329,RMVar_hsa_circ_372873,RMVar_hsa_circ_353830,RMVar_hsa_circ_47548,RMVar_hsa_circ_323505,RMVar_hsa_circ_46913,RMVar_hsa_circ_118407,RMVar_hsa_circ_165705,RMVar_hsa_circ_165706,RMVar_hsa_circ_165704,RMVar_hsa_circ_374498,RMVar_hsa_circ_268993,RMVar_hsa_circ_344767,RMVar_hsa_circ_265432,RMVar_hsa_circ_110425,RMVar_hsa_circ_113365,RMVar_hsa_circ_46289,RMVar_hsa_circ_113638,RMVar_hsa_circ_165709,RMVar_hsa_circ_165711,RMVar_hsa_circ_165713,RMVar_hsa_circ_165714,RMVar_hsa_circ_165712,RMVar_hsa_circ_165710,RMVar_hsa_circ_339111,RMVar_hsa_circ_376105,RMVar_hsa_circ_353269,RMVar_hsa_circ_286646,RMVar_hsa_circ_54418,RMVar_hsa_circ_94685,RMVar_hsa_circ_50106,RMVar_hsa_circ_47081,RMVar_hsa_circ_165716,RMVar_hsa_circ_165718,RMVar_hsa_circ_165719,RMVar_hsa_circ_165717,RMVar_hsa_circ_336134,RMVar_hsa_circ_357854,RMVar_hsa_circ_165715,RMVar_hsa_circ_361029,RMVar_hsa_circ_337444,RMVar_hsa_circ_102824,RMVar_hsa_circ_307917,RMVar_hsa_circ_69700,RMVar_hsa_circ_165721,RMVar_hsa_circ_45136,RMVar_hsa_circ_165722 25562 RMVar_ID_25562 Human_SNP_ID_549967774 A-to-I Human chr14 - 31342204 31342204 31342204 TTTTTTCTTTTTTGTAGAGACAGGGTCTTGCTATGTTACCCAGGCTGGTCTTGAACTTCTGGTCT TTTTTTCTTTTTTGTAGAGACAGGGTCTTGCTGTGTTACCCAGGCTGGTCTTGAACTTCTGGTCT T C AL139353.1,HEATR5A Ensembl:ENSG00000203546,Ensembl:ENSG00000129493 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs567543563 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44428,RMVar_hsa_circ_86159,RMVar_hsa_circ_119850,RMVar_hsa_circ_95747,RMVar_hsa_circ_165680,RMVar_hsa_circ_165681,RMVar_hsa_circ_165679,RMVar_hsa_circ_368289,RMVar_hsa_circ_278379,RMVar_hsa_circ_327225,RMVar_hsa_circ_353324,RMVar_hsa_circ_343730,RMVar_hsa_circ_336399,RMVar_hsa_circ_115772,RMVar_hsa_circ_116723,RMVar_hsa_circ_99941,RMVar_hsa_circ_165686,RMVar_hsa_circ_165688,RMVar_hsa_circ_165689,RMVar_hsa_circ_165687,RMVar_hsa_circ_78668,RMVar_hsa_circ_375049,RMVar_hsa_circ_165698,RMVar_hsa_circ_20391,RMVar_hsa_circ_165697,RMVar_hsa_circ_90560,RMVar_hsa_circ_54292,RMVar_hsa_circ_2808,RMVar_hsa_circ_7643,RMVar_hsa_circ_165702,RMVar_hsa_circ_165703,RMVar_hsa_circ_372873,RMVar_hsa_circ_47548,RMVar_hsa_circ_46913,RMVar_hsa_circ_118407,RMVar_hsa_circ_165704,RMVar_hsa_circ_268993,RMVar_hsa_circ_265432,RMVar_hsa_circ_113365,RMVar_hsa_circ_165713,RMVar_hsa_circ_165714,RMVar_hsa_circ_339111,RMVar_hsa_circ_94685,RMVar_hsa_circ_50106,RMVar_hsa_circ_47081,RMVar_hsa_circ_165716,RMVar_hsa_circ_357854,RMVar_hsa_circ_165715,RMVar_hsa_circ_337444,RMVar_hsa_circ_102824,RMVar_hsa_circ_45136,RMVar_hsa_circ_165722,RMVar_hsa_circ_361267,RMVar_hsa_circ_115661,RMVar_hsa_circ_102772,RMVar_hsa_circ_364060,RMVar_hsa_circ_165724,RMVar_hsa_circ_165725,RMVar_hsa_circ_165723,RMVar_hsa_circ_327937,RMVar_hsa_circ_342074,RMVar_hsa_circ_48124,RMVar_hsa_circ_327498,RMVar_hsa_circ_297360,RMVar_hsa_circ_42893,RMVar_hsa_circ_90831,RMVar_hsa_circ_165731,RMVar_hsa_circ_311548,RMVar_hsa_circ_291412,RMVar_hsa_circ_165730,RMVar_hsa_circ_265515,RMVar_hsa_circ_318504,RMVar_hsa_circ_359348,RMVar_hsa_circ_165732,RMVar_hsa_circ_350701,RMVar_hsa_circ_294406,RMVar_hsa_circ_107730,RMVar_hsa_circ_46516,RMVar_hsa_circ_165734,RMVar_hsa_circ_165736,RMVar_hsa_circ_165738,RMVar_hsa_circ_61180,RMVar_hsa_circ_165737,RMVar_hsa_circ_165735,RMVar_hsa_circ_165733 25563 RMVar_ID_25563 Human_SNP_ID_549967784 A-to-I Human chr14 - 31342239 31342239 31342239 GGACTACAGTAAAGTACCACCACACCTAGCTAATTTTTTTTCTTTTTTGTAGAGACAGGGTCTTG GGACTACAGTAAAGTACCACCACACCTAGCTATTTTTTTTTCTTTTTTGTAGAGACAGGGTCTTG T A AL139353.1,HEATR5A Ensembl:ENSG00000203546,Ensembl:ENSG00000129493 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs932857600 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44428,RMVar_hsa_circ_86159,RMVar_hsa_circ_119850,RMVar_hsa_circ_95747,RMVar_hsa_circ_165680,RMVar_hsa_circ_165681,RMVar_hsa_circ_165679,RMVar_hsa_circ_368289,RMVar_hsa_circ_278379,RMVar_hsa_circ_327225,RMVar_hsa_circ_353324,RMVar_hsa_circ_343730,RMVar_hsa_circ_336399,RMVar_hsa_circ_115772,RMVar_hsa_circ_116723,RMVar_hsa_circ_99941,RMVar_hsa_circ_165686,RMVar_hsa_circ_165688,RMVar_hsa_circ_165689,RMVar_hsa_circ_165687,RMVar_hsa_circ_78668,RMVar_hsa_circ_375049,RMVar_hsa_circ_165698,RMVar_hsa_circ_20391,RMVar_hsa_circ_165697,RMVar_hsa_circ_90560,RMVar_hsa_circ_54292,RMVar_hsa_circ_2808,RMVar_hsa_circ_7643,RMVar_hsa_circ_165702,RMVar_hsa_circ_165703,RMVar_hsa_circ_372873,RMVar_hsa_circ_47548,RMVar_hsa_circ_46913,RMVar_hsa_circ_118407,RMVar_hsa_circ_165704,RMVar_hsa_circ_268993,RMVar_hsa_circ_265432,RMVar_hsa_circ_113365,RMVar_hsa_circ_165713,RMVar_hsa_circ_165714,RMVar_hsa_circ_339111,RMVar_hsa_circ_94685,RMVar_hsa_circ_50106,RMVar_hsa_circ_47081,RMVar_hsa_circ_165716,RMVar_hsa_circ_357854,RMVar_hsa_circ_165715,RMVar_hsa_circ_337444,RMVar_hsa_circ_102824,RMVar_hsa_circ_45136,RMVar_hsa_circ_165722,RMVar_hsa_circ_361267,RMVar_hsa_circ_115661,RMVar_hsa_circ_102772,RMVar_hsa_circ_364060,RMVar_hsa_circ_165724,RMVar_hsa_circ_165725,RMVar_hsa_circ_165723,RMVar_hsa_circ_327937,RMVar_hsa_circ_342074,RMVar_hsa_circ_48124,RMVar_hsa_circ_327498,RMVar_hsa_circ_297360,RMVar_hsa_circ_42893,RMVar_hsa_circ_90831,RMVar_hsa_circ_165731,RMVar_hsa_circ_311548,RMVar_hsa_circ_291412,RMVar_hsa_circ_165730,RMVar_hsa_circ_265515,RMVar_hsa_circ_318504,RMVar_hsa_circ_359348,RMVar_hsa_circ_165732,RMVar_hsa_circ_350701,RMVar_hsa_circ_294406,RMVar_hsa_circ_107730,RMVar_hsa_circ_46516,RMVar_hsa_circ_165734,RMVar_hsa_circ_165736,RMVar_hsa_circ_165738,RMVar_hsa_circ_61180,RMVar_hsa_circ_165737,RMVar_hsa_circ_165735,RMVar_hsa_circ_165733 25564 RMVar_ID_25564 Human_SNP_ID_549967788 A-to-I Human chr14 - 31342266 31342266 31342266 CTCCCCCTTCAGCCTCCGAAGTAGCTCGGACTACAGTAAAGTACCACCACACCTAGCTAATTTTT CTCCCCCTTCAGCCTCCGAAGTAGCTCGGACTGCAGTAAAGTACCACCACACCTAGCTAATTTTT T C AL139353.1,HEATR5A Ensembl:ENSG00000203546,Ensembl:ENSG00000129493 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991890430 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44428,RMVar_hsa_circ_86159,RMVar_hsa_circ_119850,RMVar_hsa_circ_95747,RMVar_hsa_circ_165680,RMVar_hsa_circ_165681,RMVar_hsa_circ_165679,RMVar_hsa_circ_368289,RMVar_hsa_circ_278379,RMVar_hsa_circ_327225,RMVar_hsa_circ_353324,RMVar_hsa_circ_343730,RMVar_hsa_circ_336399,RMVar_hsa_circ_115772,RMVar_hsa_circ_116723,RMVar_hsa_circ_99941,RMVar_hsa_circ_165686,RMVar_hsa_circ_165688,RMVar_hsa_circ_165689,RMVar_hsa_circ_165687,RMVar_hsa_circ_78668,RMVar_hsa_circ_375049,RMVar_hsa_circ_165698,RMVar_hsa_circ_20391,RMVar_hsa_circ_165697,RMVar_hsa_circ_90560,RMVar_hsa_circ_54292,RMVar_hsa_circ_2808,RMVar_hsa_circ_7643,RMVar_hsa_circ_165702,RMVar_hsa_circ_165703,RMVar_hsa_circ_372873,RMVar_hsa_circ_47548,RMVar_hsa_circ_46913,RMVar_hsa_circ_118407,RMVar_hsa_circ_165704,RMVar_hsa_circ_268993,RMVar_hsa_circ_265432,RMVar_hsa_circ_113365,RMVar_hsa_circ_165713,RMVar_hsa_circ_165714,RMVar_hsa_circ_339111,RMVar_hsa_circ_94685,RMVar_hsa_circ_50106,RMVar_hsa_circ_47081,RMVar_hsa_circ_165716,RMVar_hsa_circ_357854,RMVar_hsa_circ_165715,RMVar_hsa_circ_337444,RMVar_hsa_circ_102824,RMVar_hsa_circ_45136,RMVar_hsa_circ_165722,RMVar_hsa_circ_361267,RMVar_hsa_circ_115661,RMVar_hsa_circ_102772,RMVar_hsa_circ_364060,RMVar_hsa_circ_165724,RMVar_hsa_circ_165725,RMVar_hsa_circ_165723,RMVar_hsa_circ_327937,RMVar_hsa_circ_342074,RMVar_hsa_circ_48124,RMVar_hsa_circ_327498,RMVar_hsa_circ_297360,RMVar_hsa_circ_42893,RMVar_hsa_circ_90831,RMVar_hsa_circ_165731,RMVar_hsa_circ_311548,RMVar_hsa_circ_291412,RMVar_hsa_circ_165730,RMVar_hsa_circ_265515,RMVar_hsa_circ_318504,RMVar_hsa_circ_359348,RMVar_hsa_circ_165732,RMVar_hsa_circ_350701,RMVar_hsa_circ_294406,RMVar_hsa_circ_107730,RMVar_hsa_circ_46516,RMVar_hsa_circ_165734,RMVar_hsa_circ_165736,RMVar_hsa_circ_165738,RMVar_hsa_circ_61180,RMVar_hsa_circ_165737,RMVar_hsa_circ_165735,RMVar_hsa_circ_165733 25565 RMVar_ID_25565 Human_SNP_ID_549967791 A-to-I Human chr14 - 31342279 31342279 31342279 GGCTCAAGTGATCCTCCCCCTTCAGCCTCCGAAGTAGCTCGGACTACAGTAAAGTACCACCACAC GGCTCAAGTGATCCTCCCCCTTCAGCCTCCGAGGTAGCTCGGACTACAGTAAAGTACCACCACAC T C AL139353.1,HEATR5A Ensembl:ENSG00000203546,Ensembl:ENSG00000129493 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs77738195 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44428,RMVar_hsa_circ_86159,RMVar_hsa_circ_119850,RMVar_hsa_circ_95747,RMVar_hsa_circ_165680,RMVar_hsa_circ_165681,RMVar_hsa_circ_165679,RMVar_hsa_circ_368289,RMVar_hsa_circ_278379,RMVar_hsa_circ_327225,RMVar_hsa_circ_353324,RMVar_hsa_circ_343730,RMVar_hsa_circ_336399,RMVar_hsa_circ_115772,RMVar_hsa_circ_116723,RMVar_hsa_circ_99941,RMVar_hsa_circ_165686,RMVar_hsa_circ_165688,RMVar_hsa_circ_165689,RMVar_hsa_circ_165687,RMVar_hsa_circ_78668,RMVar_hsa_circ_375049,RMVar_hsa_circ_165698,RMVar_hsa_circ_20391,RMVar_hsa_circ_165697,RMVar_hsa_circ_90560,RMVar_hsa_circ_54292,RMVar_hsa_circ_2808,RMVar_hsa_circ_7643,RMVar_hsa_circ_165702,RMVar_hsa_circ_165703,RMVar_hsa_circ_372873,RMVar_hsa_circ_47548,RMVar_hsa_circ_46913,RMVar_hsa_circ_118407,RMVar_hsa_circ_165704,RMVar_hsa_circ_268993,RMVar_hsa_circ_265432,RMVar_hsa_circ_113365,RMVar_hsa_circ_165713,RMVar_hsa_circ_165714,RMVar_hsa_circ_339111,RMVar_hsa_circ_94685,RMVar_hsa_circ_50106,RMVar_hsa_circ_47081,RMVar_hsa_circ_165716,RMVar_hsa_circ_357854,RMVar_hsa_circ_165715,RMVar_hsa_circ_337444,RMVar_hsa_circ_102824,RMVar_hsa_circ_45136,RMVar_hsa_circ_165722,RMVar_hsa_circ_361267,RMVar_hsa_circ_115661,RMVar_hsa_circ_102772,RMVar_hsa_circ_364060,RMVar_hsa_circ_165724,RMVar_hsa_circ_165725,RMVar_hsa_circ_165723,RMVar_hsa_circ_327937,RMVar_hsa_circ_342074,RMVar_hsa_circ_48124,RMVar_hsa_circ_327498,RMVar_hsa_circ_297360,RMVar_hsa_circ_42893,RMVar_hsa_circ_90831,RMVar_hsa_circ_165731,RMVar_hsa_circ_311548,RMVar_hsa_circ_291412,RMVar_hsa_circ_165730,RMVar_hsa_circ_265515,RMVar_hsa_circ_318504,RMVar_hsa_circ_359348,RMVar_hsa_circ_165732,RMVar_hsa_circ_350701,RMVar_hsa_circ_294406,RMVar_hsa_circ_107730,RMVar_hsa_circ_46516,RMVar_hsa_circ_165734,RMVar_hsa_circ_165736,RMVar_hsa_circ_165738,RMVar_hsa_circ_61180,RMVar_hsa_circ_165737,RMVar_hsa_circ_165735,RMVar_hsa_circ_165733 25566 RMVar_ID_25566 Human_SNP_ID_549967816 A-to-I Human chr14 - 31342362 31342362 31342362 TATTTATTTTAGAGGCACAGTCTCACTTTGTCAGGCTGGAGTGCGGTGGTGCAATCATAGCTCAC TATTTATTTTAGAGGCACAGTCTCACTTTGTCGGGCTGGAGTGCGGTGGTGCAATCATAGCTCAC T C AL139353.1,HEATR5A Ensembl:ENSG00000203546,Ensembl:ENSG00000129493 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1033548055 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44428,RMVar_hsa_circ_86159,RMVar_hsa_circ_119850,RMVar_hsa_circ_95747,RMVar_hsa_circ_165680,RMVar_hsa_circ_165681,RMVar_hsa_circ_165679,RMVar_hsa_circ_368289,RMVar_hsa_circ_278379,RMVar_hsa_circ_327225,RMVar_hsa_circ_353324,RMVar_hsa_circ_343730,RMVar_hsa_circ_336399,RMVar_hsa_circ_115772,RMVar_hsa_circ_116723,RMVar_hsa_circ_99941,RMVar_hsa_circ_165686,RMVar_hsa_circ_165688,RMVar_hsa_circ_165689,RMVar_hsa_circ_165687,RMVar_hsa_circ_78668,RMVar_hsa_circ_375049,RMVar_hsa_circ_165698,RMVar_hsa_circ_20391,RMVar_hsa_circ_165697,RMVar_hsa_circ_90560,RMVar_hsa_circ_54292,RMVar_hsa_circ_2808,RMVar_hsa_circ_7643,RMVar_hsa_circ_165702,RMVar_hsa_circ_165703,RMVar_hsa_circ_372873,RMVar_hsa_circ_47548,RMVar_hsa_circ_46913,RMVar_hsa_circ_118407,RMVar_hsa_circ_165704,RMVar_hsa_circ_268993,RMVar_hsa_circ_265432,RMVar_hsa_circ_113365,RMVar_hsa_circ_165713,RMVar_hsa_circ_165714,RMVar_hsa_circ_339111,RMVar_hsa_circ_94685,RMVar_hsa_circ_50106,RMVar_hsa_circ_47081,RMVar_hsa_circ_165716,RMVar_hsa_circ_357854,RMVar_hsa_circ_165715,RMVar_hsa_circ_337444,RMVar_hsa_circ_102824,RMVar_hsa_circ_45136,RMVar_hsa_circ_165722,RMVar_hsa_circ_361267,RMVar_hsa_circ_115661,RMVar_hsa_circ_102772,RMVar_hsa_circ_364060,RMVar_hsa_circ_165724,RMVar_hsa_circ_165725,RMVar_hsa_circ_165723,RMVar_hsa_circ_327937,RMVar_hsa_circ_342074,RMVar_hsa_circ_48124,RMVar_hsa_circ_327498,RMVar_hsa_circ_297360,RMVar_hsa_circ_42893,RMVar_hsa_circ_90831,RMVar_hsa_circ_165731,RMVar_hsa_circ_311548,RMVar_hsa_circ_291412,RMVar_hsa_circ_165730,RMVar_hsa_circ_265515,RMVar_hsa_circ_318504,RMVar_hsa_circ_359348,RMVar_hsa_circ_165732,RMVar_hsa_circ_350701,RMVar_hsa_circ_294406,RMVar_hsa_circ_107730,RMVar_hsa_circ_46516,RMVar_hsa_circ_165734,RMVar_hsa_circ_165736,RMVar_hsa_circ_165738,RMVar_hsa_circ_61180,RMVar_hsa_circ_165737,RMVar_hsa_circ_165735,RMVar_hsa_circ_165733 25567 RMVar_ID_25567 Human_SNP_ID_549970224 A-to-I Human chr14 - 31351752 31351752 31351752 AAAAATTAGCAGGGTGTGGGTAATGTGTTCCTATACTCCCAGGTACTTTGGTGGCTGAGGCTGGA AAAAATTAGCAGGGTGTGGGTAATGTGTTCCTGTACTCCCAGGTACTTTGGTGGCTGAGGCTGGA T C AL139353.1,HEATR5A Ensembl:ENSG00000203546,Ensembl:ENSG00000129493 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928222709 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_663,RMVar_hsa_circ_44428,RMVar_hsa_circ_86159,RMVar_hsa_circ_119850,RMVar_hsa_circ_95747,RMVar_hsa_circ_165680,RMVar_hsa_circ_165681,RMVar_hsa_circ_165679,RMVar_hsa_circ_278379,RMVar_hsa_circ_343730,RMVar_hsa_circ_336399,RMVar_hsa_circ_115772,RMVar_hsa_circ_116723,RMVar_hsa_circ_99941,RMVar_hsa_circ_165686,RMVar_hsa_circ_165688,RMVar_hsa_circ_165689,RMVar_hsa_circ_165687,RMVar_hsa_circ_78668,RMVar_hsa_circ_165698,RMVar_hsa_circ_90560,RMVar_hsa_circ_2808,RMVar_hsa_circ_165702,RMVar_hsa_circ_165703,RMVar_hsa_circ_118407,RMVar_hsa_circ_268993,RMVar_hsa_circ_265432,RMVar_hsa_circ_165714,RMVar_hsa_circ_339111,RMVar_hsa_circ_94685,RMVar_hsa_circ_165716,RMVar_hsa_circ_357854,RMVar_hsa_circ_165715,RMVar_hsa_circ_102824,RMVar_hsa_circ_165722,RMVar_hsa_circ_102772,RMVar_hsa_circ_165723,RMVar_hsa_circ_327937,RMVar_hsa_circ_48124,RMVar_hsa_circ_42893,RMVar_hsa_circ_90831,RMVar_hsa_circ_165731,RMVar_hsa_circ_311548,RMVar_hsa_circ_265515,RMVar_hsa_circ_318504,RMVar_hsa_circ_165732,RMVar_hsa_circ_350701,RMVar_hsa_circ_107730,RMVar_hsa_circ_165734,RMVar_hsa_circ_165736,RMVar_hsa_circ_61180,RMVar_hsa_circ_165735,RMVar_hsa_circ_165733,RMVar_hsa_circ_101689,RMVar_hsa_circ_286417,RMVar_hsa_circ_357865,RMVar_hsa_circ_371484,RMVar_hsa_circ_111300,RMVar_hsa_circ_42119,RMVar_hsa_circ_15725,RMVar_hsa_circ_106760,RMVar_hsa_circ_68462,RMVar_hsa_circ_165741,RMVar_hsa_circ_165742,RMVar_hsa_circ_165743,RMVar_hsa_circ_165740,RMVar_hsa_circ_373117,RMVar_hsa_circ_86572,RMVar_hsa_circ_165744,RMVar_hsa_circ_165745,RMVar_hsa_circ_295503,RMVar_hsa_circ_363230,RMVar_hsa_circ_364582,RMVar_hsa_circ_120359,RMVar_hsa_circ_23697,RMVar_hsa_circ_165749,RMVar_hsa_circ_165750,RMVar_hsa_circ_165748,RMVar_hsa_circ_294611,RMVar_hsa_circ_295333,RMVar_hsa_circ_122682,RMVar_hsa_circ_88463,RMVar_hsa_circ_165752,RMVar_hsa_circ_165753,RMVar_hsa_circ_303803,RMVar_hsa_circ_165751,RMVar_hsa_circ_266145,RMVar_hsa_circ_165754 25568 RMVar_ID_25568 Human_SNP_ID_549970252 A-to-I Human chr14 - 31351823 31351823 31351823 ATCGCTTGAGCTTAGGAGTTCAAGACCAGCCTAAGCAACATAGTGAGATATCATCTCTTTTAAAA ATCGCTTGAGCTTAGGAGTTCAAGACCAGCCTGAGCAACATAGTGAGATATCATCTCTTTTAAAA T C AL139353.1,HEATR5A Ensembl:ENSG00000203546,Ensembl:ENSG00000129493 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1034773547 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_663,RMVar_hsa_circ_44428,RMVar_hsa_circ_86159,RMVar_hsa_circ_119850,RMVar_hsa_circ_95747,RMVar_hsa_circ_165680,RMVar_hsa_circ_165681,RMVar_hsa_circ_165679,RMVar_hsa_circ_278379,RMVar_hsa_circ_343730,RMVar_hsa_circ_336399,RMVar_hsa_circ_115772,RMVar_hsa_circ_116723,RMVar_hsa_circ_99941,RMVar_hsa_circ_165686,RMVar_hsa_circ_165688,RMVar_hsa_circ_165689,RMVar_hsa_circ_165687,RMVar_hsa_circ_78668,RMVar_hsa_circ_165698,RMVar_hsa_circ_90560,RMVar_hsa_circ_2808,RMVar_hsa_circ_165702,RMVar_hsa_circ_165703,RMVar_hsa_circ_118407,RMVar_hsa_circ_268993,RMVar_hsa_circ_265432,RMVar_hsa_circ_165714,RMVar_hsa_circ_339111,RMVar_hsa_circ_94685,RMVar_hsa_circ_165716,RMVar_hsa_circ_357854,RMVar_hsa_circ_165715,RMVar_hsa_circ_102824,RMVar_hsa_circ_165722,RMVar_hsa_circ_102772,RMVar_hsa_circ_165723,RMVar_hsa_circ_327937,RMVar_hsa_circ_48124,RMVar_hsa_circ_42893,RMVar_hsa_circ_90831,RMVar_hsa_circ_165731,RMVar_hsa_circ_311548,RMVar_hsa_circ_265515,RMVar_hsa_circ_318504,RMVar_hsa_circ_165732,RMVar_hsa_circ_350701,RMVar_hsa_circ_107730,RMVar_hsa_circ_165734,RMVar_hsa_circ_165736,RMVar_hsa_circ_61180,RMVar_hsa_circ_165735,RMVar_hsa_circ_165733,RMVar_hsa_circ_101689,RMVar_hsa_circ_286417,RMVar_hsa_circ_357865,RMVar_hsa_circ_371484,RMVar_hsa_circ_111300,RMVar_hsa_circ_42119,RMVar_hsa_circ_15725,RMVar_hsa_circ_106760,RMVar_hsa_circ_68462,RMVar_hsa_circ_165741,RMVar_hsa_circ_165742,RMVar_hsa_circ_165743,RMVar_hsa_circ_165740,RMVar_hsa_circ_373117,RMVar_hsa_circ_86572,RMVar_hsa_circ_165744,RMVar_hsa_circ_165745,RMVar_hsa_circ_295503,RMVar_hsa_circ_363230,RMVar_hsa_circ_364582,RMVar_hsa_circ_120359,RMVar_hsa_circ_23697,RMVar_hsa_circ_165749,RMVar_hsa_circ_165750,RMVar_hsa_circ_165748,RMVar_hsa_circ_294611,RMVar_hsa_circ_295333,RMVar_hsa_circ_122682,RMVar_hsa_circ_88463,RMVar_hsa_circ_165752,RMVar_hsa_circ_165753,RMVar_hsa_circ_303803,RMVar_hsa_circ_165751,RMVar_hsa_circ_266145,RMVar_hsa_circ_165754 25569 RMVar_ID_25569 Human_SNP_ID_549970634 A-to-I Human chr14 - 31353485 31353485 31353485 GCGATCCTCCTGCCTCTGCCGCCCAAAGTGCTAGAATTACAGGCGTGAGCCACCAGAAAAATTTT GCGATCCTCCTGCCTCTGCCGCCCAAAGTGCTGGAATTACAGGCGTGAGCCACCAGAAAAATTTT T C AL139353.1,HEATR5A Ensembl:ENSG00000203546,Ensembl:ENSG00000129493 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904782651 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12315430 RMVar_hsa_circ_663,RMVar_hsa_circ_44428,RMVar_hsa_circ_86159,RMVar_hsa_circ_119850,RMVar_hsa_circ_95747,RMVar_hsa_circ_165680,RMVar_hsa_circ_165681,RMVar_hsa_circ_165679,RMVar_hsa_circ_278379,RMVar_hsa_circ_343730,RMVar_hsa_circ_336399,RMVar_hsa_circ_115772,RMVar_hsa_circ_116723,RMVar_hsa_circ_99941,RMVar_hsa_circ_165686,RMVar_hsa_circ_165688,RMVar_hsa_circ_165689,RMVar_hsa_circ_165687,RMVar_hsa_circ_78668,RMVar_hsa_circ_165698,RMVar_hsa_circ_90560,RMVar_hsa_circ_2808,RMVar_hsa_circ_165702,RMVar_hsa_circ_165703,RMVar_hsa_circ_118407,RMVar_hsa_circ_268993,RMVar_hsa_circ_265432,RMVar_hsa_circ_165714,RMVar_hsa_circ_339111,RMVar_hsa_circ_94685,RMVar_hsa_circ_165716,RMVar_hsa_circ_357854,RMVar_hsa_circ_165715,RMVar_hsa_circ_102824,RMVar_hsa_circ_165722,RMVar_hsa_circ_102772,RMVar_hsa_circ_165723,RMVar_hsa_circ_327937,RMVar_hsa_circ_48124,RMVar_hsa_circ_42893,RMVar_hsa_circ_90831,RMVar_hsa_circ_165731,RMVar_hsa_circ_311548,RMVar_hsa_circ_265515,RMVar_hsa_circ_318504,RMVar_hsa_circ_165732,RMVar_hsa_circ_350701,RMVar_hsa_circ_107730,RMVar_hsa_circ_165734,RMVar_hsa_circ_165736,RMVar_hsa_circ_61180,RMVar_hsa_circ_165735,RMVar_hsa_circ_165733,RMVar_hsa_circ_101689,RMVar_hsa_circ_286417,RMVar_hsa_circ_357865,RMVar_hsa_circ_371484,RMVar_hsa_circ_111300,RMVar_hsa_circ_42119,RMVar_hsa_circ_15725,RMVar_hsa_circ_106760,RMVar_hsa_circ_68462,RMVar_hsa_circ_165741,RMVar_hsa_circ_165742,RMVar_hsa_circ_165743,RMVar_hsa_circ_165740,RMVar_hsa_circ_373117,RMVar_hsa_circ_86572,RMVar_hsa_circ_165744,RMVar_hsa_circ_165745,RMVar_hsa_circ_295503,RMVar_hsa_circ_363230,RMVar_hsa_circ_364582,RMVar_hsa_circ_120359,RMVar_hsa_circ_23697,RMVar_hsa_circ_165749,RMVar_hsa_circ_165750,RMVar_hsa_circ_165748,RMVar_hsa_circ_294611,RMVar_hsa_circ_295333,RMVar_hsa_circ_122682,RMVar_hsa_circ_88463,RMVar_hsa_circ_165752,RMVar_hsa_circ_165753,RMVar_hsa_circ_303803,RMVar_hsa_circ_165751,RMVar_hsa_circ_266145,RMVar_hsa_circ_165754 25570 RMVar_ID_25570 Human_SNP_ID_549970654 A-to-I Human chr14 - 31353553 31353553 31353553 TTTTTTCTTTTTAGTGGAGATAAGGTCTCACTATGTTGCCTAGGCTGGTCTCGAACTCATGGGCT TTTTTTCTTTTTAGTGGAGATAAGGTCTCACTGTGTTGCCTAGGCTGGTCTCGAACTCATGGGCT T C AL139353.1,HEATR5A Ensembl:ENSG00000203546,Ensembl:ENSG00000129493 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049975840 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_663,RMVar_hsa_circ_44428,RMVar_hsa_circ_86159,RMVar_hsa_circ_119850,RMVar_hsa_circ_95747,RMVar_hsa_circ_165680,RMVar_hsa_circ_165681,RMVar_hsa_circ_165679,RMVar_hsa_circ_278379,RMVar_hsa_circ_343730,RMVar_hsa_circ_336399,RMVar_hsa_circ_115772,RMVar_hsa_circ_116723,RMVar_hsa_circ_99941,RMVar_hsa_circ_165686,RMVar_hsa_circ_165688,RMVar_hsa_circ_165689,RMVar_hsa_circ_165687,RMVar_hsa_circ_78668,RMVar_hsa_circ_165698,RMVar_hsa_circ_90560,RMVar_hsa_circ_2808,RMVar_hsa_circ_165702,RMVar_hsa_circ_165703,RMVar_hsa_circ_118407,RMVar_hsa_circ_268993,RMVar_hsa_circ_265432,RMVar_hsa_circ_165714,RMVar_hsa_circ_339111,RMVar_hsa_circ_94685,RMVar_hsa_circ_165716,RMVar_hsa_circ_357854,RMVar_hsa_circ_165715,RMVar_hsa_circ_102824,RMVar_hsa_circ_165722,RMVar_hsa_circ_102772,RMVar_hsa_circ_165723,RMVar_hsa_circ_327937,RMVar_hsa_circ_48124,RMVar_hsa_circ_42893,RMVar_hsa_circ_90831,RMVar_hsa_circ_165731,RMVar_hsa_circ_311548,RMVar_hsa_circ_265515,RMVar_hsa_circ_318504,RMVar_hsa_circ_165732,RMVar_hsa_circ_350701,RMVar_hsa_circ_107730,RMVar_hsa_circ_165734,RMVar_hsa_circ_165736,RMVar_hsa_circ_61180,RMVar_hsa_circ_165735,RMVar_hsa_circ_165733,RMVar_hsa_circ_101689,RMVar_hsa_circ_286417,RMVar_hsa_circ_357865,RMVar_hsa_circ_371484,RMVar_hsa_circ_111300,RMVar_hsa_circ_42119,RMVar_hsa_circ_15725,RMVar_hsa_circ_106760,RMVar_hsa_circ_68462,RMVar_hsa_circ_165741,RMVar_hsa_circ_165742,RMVar_hsa_circ_165743,RMVar_hsa_circ_165740,RMVar_hsa_circ_373117,RMVar_hsa_circ_86572,RMVar_hsa_circ_165744,RMVar_hsa_circ_165745,RMVar_hsa_circ_295503,RMVar_hsa_circ_363230,RMVar_hsa_circ_364582,RMVar_hsa_circ_120359,RMVar_hsa_circ_23697,RMVar_hsa_circ_165749,RMVar_hsa_circ_165750,RMVar_hsa_circ_165748,RMVar_hsa_circ_294611,RMVar_hsa_circ_295333,RMVar_hsa_circ_122682,RMVar_hsa_circ_88463,RMVar_hsa_circ_165752,RMVar_hsa_circ_165753,RMVar_hsa_circ_303803,RMVar_hsa_circ_165751,RMVar_hsa_circ_266145,RMVar_hsa_circ_165754 25571 RMVar_ID_25571 Human_SNP_ID_549970679 A-to-I Human chr14 - 31353679 31353679 31353679 CAGGCTGGAATGCAGTGGTGCTATTTTGCCTCACTGCAGCTTCAGTCTCCCAAGCTCAAGCAATC CAGGCTGGAATGCAGTGGTGCTATTTTGCCTCGCTGCAGCTTCAGTCTCCCAAGCTCAAGCAATC T C AL139353.1,HEATR5A Ensembl:ENSG00000203546,Ensembl:ENSG00000129493 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs952520690 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_663,RMVar_hsa_circ_44428,RMVar_hsa_circ_86159,RMVar_hsa_circ_119850,RMVar_hsa_circ_95747,RMVar_hsa_circ_165680,RMVar_hsa_circ_165681,RMVar_hsa_circ_165679,RMVar_hsa_circ_278379,RMVar_hsa_circ_343730,RMVar_hsa_circ_336399,RMVar_hsa_circ_115772,RMVar_hsa_circ_116723,RMVar_hsa_circ_99941,RMVar_hsa_circ_165686,RMVar_hsa_circ_165688,RMVar_hsa_circ_165689,RMVar_hsa_circ_165687,RMVar_hsa_circ_78668,RMVar_hsa_circ_165698,RMVar_hsa_circ_90560,RMVar_hsa_circ_2808,RMVar_hsa_circ_165702,RMVar_hsa_circ_165703,RMVar_hsa_circ_118407,RMVar_hsa_circ_268993,RMVar_hsa_circ_265432,RMVar_hsa_circ_165714,RMVar_hsa_circ_339111,RMVar_hsa_circ_94685,RMVar_hsa_circ_165716,RMVar_hsa_circ_357854,RMVar_hsa_circ_165715,RMVar_hsa_circ_102824,RMVar_hsa_circ_165722,RMVar_hsa_circ_102772,RMVar_hsa_circ_165723,RMVar_hsa_circ_327937,RMVar_hsa_circ_48124,RMVar_hsa_circ_42893,RMVar_hsa_circ_90831,RMVar_hsa_circ_165731,RMVar_hsa_circ_311548,RMVar_hsa_circ_265515,RMVar_hsa_circ_318504,RMVar_hsa_circ_165732,RMVar_hsa_circ_350701,RMVar_hsa_circ_107730,RMVar_hsa_circ_165734,RMVar_hsa_circ_165736,RMVar_hsa_circ_61180,RMVar_hsa_circ_165735,RMVar_hsa_circ_165733,RMVar_hsa_circ_101689,RMVar_hsa_circ_286417,RMVar_hsa_circ_357865,RMVar_hsa_circ_371484,RMVar_hsa_circ_111300,RMVar_hsa_circ_42119,RMVar_hsa_circ_15725,RMVar_hsa_circ_106760,RMVar_hsa_circ_68462,RMVar_hsa_circ_165741,RMVar_hsa_circ_165742,RMVar_hsa_circ_165743,RMVar_hsa_circ_165740,RMVar_hsa_circ_373117,RMVar_hsa_circ_86572,RMVar_hsa_circ_165744,RMVar_hsa_circ_165745,RMVar_hsa_circ_295503,RMVar_hsa_circ_363230,RMVar_hsa_circ_364582,RMVar_hsa_circ_120359,RMVar_hsa_circ_23697,RMVar_hsa_circ_165749,RMVar_hsa_circ_165750,RMVar_hsa_circ_165748,RMVar_hsa_circ_294611,RMVar_hsa_circ_295333,RMVar_hsa_circ_122682,RMVar_hsa_circ_88463,RMVar_hsa_circ_165752,RMVar_hsa_circ_165753,RMVar_hsa_circ_303803,RMVar_hsa_circ_165751,RMVar_hsa_circ_266145,RMVar_hsa_circ_165754 25572 RMVar_ID_25572 Human_SNP_ID_549970755 A-to-I Human chr14 - 31353897 31353897 31353897 TACTCAGGAGGCTGAGACACAAGAATGGCATGAACCTGGGAGGCAGAGCTTGCAGTGAGTTGAGA TACTCAGGAGGCTGAGACACAAGAATGGCATGGACCTGGGAGGCAGAGCTTGCAGTGAGTTGAGA T C AL139353.1,HEATR5A Ensembl:ENSG00000203546,Ensembl:ENSG00000129493 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1384050463 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_663,RMVar_hsa_circ_44428,RMVar_hsa_circ_86159,RMVar_hsa_circ_119850,RMVar_hsa_circ_95747,RMVar_hsa_circ_165680,RMVar_hsa_circ_165681,RMVar_hsa_circ_165679,RMVar_hsa_circ_278379,RMVar_hsa_circ_343730,RMVar_hsa_circ_336399,RMVar_hsa_circ_115772,RMVar_hsa_circ_116723,RMVar_hsa_circ_99941,RMVar_hsa_circ_165686,RMVar_hsa_circ_165688,RMVar_hsa_circ_165689,RMVar_hsa_circ_165687,RMVar_hsa_circ_78668,RMVar_hsa_circ_165698,RMVar_hsa_circ_90560,RMVar_hsa_circ_2808,RMVar_hsa_circ_165702,RMVar_hsa_circ_165703,RMVar_hsa_circ_118407,RMVar_hsa_circ_268993,RMVar_hsa_circ_265432,RMVar_hsa_circ_165714,RMVar_hsa_circ_339111,RMVar_hsa_circ_94685,RMVar_hsa_circ_165716,RMVar_hsa_circ_357854,RMVar_hsa_circ_165715,RMVar_hsa_circ_102824,RMVar_hsa_circ_165722,RMVar_hsa_circ_102772,RMVar_hsa_circ_165723,RMVar_hsa_circ_327937,RMVar_hsa_circ_48124,RMVar_hsa_circ_42893,RMVar_hsa_circ_90831,RMVar_hsa_circ_165731,RMVar_hsa_circ_311548,RMVar_hsa_circ_265515,RMVar_hsa_circ_318504,RMVar_hsa_circ_165732,RMVar_hsa_circ_350701,RMVar_hsa_circ_107730,RMVar_hsa_circ_165734,RMVar_hsa_circ_165736,RMVar_hsa_circ_61180,RMVar_hsa_circ_165735,RMVar_hsa_circ_165733,RMVar_hsa_circ_101689,RMVar_hsa_circ_286417,RMVar_hsa_circ_357865,RMVar_hsa_circ_371484,RMVar_hsa_circ_111300,RMVar_hsa_circ_42119,RMVar_hsa_circ_15725,RMVar_hsa_circ_106760,RMVar_hsa_circ_68462,RMVar_hsa_circ_165741,RMVar_hsa_circ_165742,RMVar_hsa_circ_165743,RMVar_hsa_circ_165740,RMVar_hsa_circ_373117,RMVar_hsa_circ_86572,RMVar_hsa_circ_165744,RMVar_hsa_circ_165745,RMVar_hsa_circ_295503,RMVar_hsa_circ_363230,RMVar_hsa_circ_364582,RMVar_hsa_circ_120359,RMVar_hsa_circ_23697,RMVar_hsa_circ_165749,RMVar_hsa_circ_165750,RMVar_hsa_circ_165748,RMVar_hsa_circ_294611,RMVar_hsa_circ_295333,RMVar_hsa_circ_122682,RMVar_hsa_circ_88463,RMVar_hsa_circ_165752,RMVar_hsa_circ_165753,RMVar_hsa_circ_303803,RMVar_hsa_circ_165751,RMVar_hsa_circ_266145,RMVar_hsa_circ_165754 25573 RMVar_ID_25573 Human_SNP_ID_549970764 A-to-I Human chr14 - 31353938 31353938 31353938 AAAAATTAGCCAGGTGTAGTGTGGGCGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGACACAAGA AAAAATTAGCCAGGTGTAGTGTGGGCGCCTGTGGTCCCAGCTACTCAGGAGGCTGAGACACAAGA T C AL139353.1,HEATR5A Ensembl:ENSG00000203546,Ensembl:ENSG00000129493 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1191738116 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_663,RMVar_hsa_circ_44428,RMVar_hsa_circ_86159,RMVar_hsa_circ_119850,RMVar_hsa_circ_95747,RMVar_hsa_circ_165680,RMVar_hsa_circ_165681,RMVar_hsa_circ_165679,RMVar_hsa_circ_278379,RMVar_hsa_circ_343730,RMVar_hsa_circ_336399,RMVar_hsa_circ_115772,RMVar_hsa_circ_116723,RMVar_hsa_circ_99941,RMVar_hsa_circ_165686,RMVar_hsa_circ_165688,RMVar_hsa_circ_165689,RMVar_hsa_circ_165687,RMVar_hsa_circ_78668,RMVar_hsa_circ_165698,RMVar_hsa_circ_90560,RMVar_hsa_circ_2808,RMVar_hsa_circ_165702,RMVar_hsa_circ_165703,RMVar_hsa_circ_118407,RMVar_hsa_circ_268993,RMVar_hsa_circ_265432,RMVar_hsa_circ_165714,RMVar_hsa_circ_339111,RMVar_hsa_circ_94685,RMVar_hsa_circ_165716,RMVar_hsa_circ_357854,RMVar_hsa_circ_165715,RMVar_hsa_circ_102824,RMVar_hsa_circ_165722,RMVar_hsa_circ_102772,RMVar_hsa_circ_165723,RMVar_hsa_circ_327937,RMVar_hsa_circ_48124,RMVar_hsa_circ_42893,RMVar_hsa_circ_90831,RMVar_hsa_circ_165731,RMVar_hsa_circ_311548,RMVar_hsa_circ_265515,RMVar_hsa_circ_318504,RMVar_hsa_circ_165732,RMVar_hsa_circ_350701,RMVar_hsa_circ_107730,RMVar_hsa_circ_165734,RMVar_hsa_circ_165736,RMVar_hsa_circ_61180,RMVar_hsa_circ_165735,RMVar_hsa_circ_165733,RMVar_hsa_circ_101689,RMVar_hsa_circ_286417,RMVar_hsa_circ_357865,RMVar_hsa_circ_371484,RMVar_hsa_circ_111300,RMVar_hsa_circ_42119,RMVar_hsa_circ_15725,RMVar_hsa_circ_106760,RMVar_hsa_circ_68462,RMVar_hsa_circ_165741,RMVar_hsa_circ_165742,RMVar_hsa_circ_165743,RMVar_hsa_circ_165740,RMVar_hsa_circ_373117,RMVar_hsa_circ_86572,RMVar_hsa_circ_165744,RMVar_hsa_circ_165745,RMVar_hsa_circ_295503,RMVar_hsa_circ_363230,RMVar_hsa_circ_364582,RMVar_hsa_circ_120359,RMVar_hsa_circ_23697,RMVar_hsa_circ_165749,RMVar_hsa_circ_165750,RMVar_hsa_circ_165748,RMVar_hsa_circ_294611,RMVar_hsa_circ_295333,RMVar_hsa_circ_122682,RMVar_hsa_circ_88463,RMVar_hsa_circ_165752,RMVar_hsa_circ_165753,RMVar_hsa_circ_303803,RMVar_hsa_circ_165751,RMVar_hsa_circ_266145,RMVar_hsa_circ_165754 25574 RMVar_ID_25574 Human_SNP_ID_549973829 A-to-I Human chr14 - 31366184 31366184 31366184 CCATATCCTCAAACTCGTGGGCTCAAGCGATCATCTGGCCTCAGCCTCCCAAAGTGCTGGAATTA CCATATCCTCAAACTCGTGGGCTCAAGCGATCGTCTGGCCTCAGCCTCCCAAAGTGCTGGAATTA T C AL139353.1,HEATR5A Ensembl:ENSG00000203546,Ensembl:ENSG00000129493 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs993484792 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_663,RMVar_hsa_circ_119850,RMVar_hsa_circ_95747,RMVar_hsa_circ_165680,RMVar_hsa_circ_165681,RMVar_hsa_circ_278379,RMVar_hsa_circ_343730,RMVar_hsa_circ_336399,RMVar_hsa_circ_116723,RMVar_hsa_circ_99941,RMVar_hsa_circ_165686,RMVar_hsa_circ_165688,RMVar_hsa_circ_165687,RMVar_hsa_circ_78668,RMVar_hsa_circ_165698,RMVar_hsa_circ_90560,RMVar_hsa_circ_2808,RMVar_hsa_circ_165702,RMVar_hsa_circ_165703,RMVar_hsa_circ_118407,RMVar_hsa_circ_268993,RMVar_hsa_circ_165714,RMVar_hsa_circ_339111,RMVar_hsa_circ_94685,RMVar_hsa_circ_165716,RMVar_hsa_circ_165715,RMVar_hsa_circ_102824,RMVar_hsa_circ_165722,RMVar_hsa_circ_102772,RMVar_hsa_circ_165723,RMVar_hsa_circ_327937,RMVar_hsa_circ_42893,RMVar_hsa_circ_90831,RMVar_hsa_circ_165731,RMVar_hsa_circ_311548,RMVar_hsa_circ_265515,RMVar_hsa_circ_318504,RMVar_hsa_circ_165732,RMVar_hsa_circ_107730,RMVar_hsa_circ_165734,RMVar_hsa_circ_61180,RMVar_hsa_circ_165735,RMVar_hsa_circ_165733,RMVar_hsa_circ_286417,RMVar_hsa_circ_111300,RMVar_hsa_circ_42119,RMVar_hsa_circ_15725,RMVar_hsa_circ_106760,RMVar_hsa_circ_165742,RMVar_hsa_circ_165743,RMVar_hsa_circ_373117,RMVar_hsa_circ_86572,RMVar_hsa_circ_165744,RMVar_hsa_circ_165745,RMVar_hsa_circ_295503,RMVar_hsa_circ_120359,RMVar_hsa_circ_74712,RMVar_hsa_circ_23697,RMVar_hsa_circ_165749,RMVar_hsa_circ_165750,RMVar_hsa_circ_165748,RMVar_hsa_circ_294611,RMVar_hsa_circ_122682,RMVar_hsa_circ_88463,RMVar_hsa_circ_165752,RMVar_hsa_circ_165753,RMVar_hsa_circ_266145,RMVar_hsa_circ_373676,RMVar_hsa_circ_165754,RMVar_hsa_circ_300520,RMVar_hsa_circ_265529,RMVar_hsa_circ_306306,RMVar_hsa_circ_165756,RMVar_hsa_circ_165755,RMVar_hsa_circ_313334,RMVar_hsa_circ_165759,RMVar_hsa_circ_288238,RMVar_hsa_circ_165758 25575 RMVar_ID_25575 Human_SNP_ID_549973841 A-to-I Human chr14 - 31366228 31366228 31366228 AGTCTGTCGCCCGGGATTGAGTGCAGTGGCGCAGTCATAGCTCACCATATCCTCAAACTCGTGGG AGTCTGTCGCCCGGGATTGAGTGCAGTGGCGCCGTCATAGCTCACCATATCCTCAAACTCGTGGG T G AL139353.1,HEATR5A Ensembl:ENSG00000203546,Ensembl:ENSG00000129493 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1393535291 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_663,RMVar_hsa_circ_119850,RMVar_hsa_circ_95747,RMVar_hsa_circ_165680,RMVar_hsa_circ_165681,RMVar_hsa_circ_278379,RMVar_hsa_circ_343730,RMVar_hsa_circ_336399,RMVar_hsa_circ_116723,RMVar_hsa_circ_99941,RMVar_hsa_circ_165686,RMVar_hsa_circ_165688,RMVar_hsa_circ_165687,RMVar_hsa_circ_78668,RMVar_hsa_circ_165698,RMVar_hsa_circ_90560,RMVar_hsa_circ_2808,RMVar_hsa_circ_165702,RMVar_hsa_circ_165703,RMVar_hsa_circ_118407,RMVar_hsa_circ_268993,RMVar_hsa_circ_165714,RMVar_hsa_circ_339111,RMVar_hsa_circ_94685,RMVar_hsa_circ_165716,RMVar_hsa_circ_165715,RMVar_hsa_circ_102824,RMVar_hsa_circ_165722,RMVar_hsa_circ_102772,RMVar_hsa_circ_165723,RMVar_hsa_circ_327937,RMVar_hsa_circ_42893,RMVar_hsa_circ_90831,RMVar_hsa_circ_165731,RMVar_hsa_circ_311548,RMVar_hsa_circ_265515,RMVar_hsa_circ_318504,RMVar_hsa_circ_165732,RMVar_hsa_circ_107730,RMVar_hsa_circ_165734,RMVar_hsa_circ_61180,RMVar_hsa_circ_165735,RMVar_hsa_circ_165733,RMVar_hsa_circ_286417,RMVar_hsa_circ_111300,RMVar_hsa_circ_42119,RMVar_hsa_circ_15725,RMVar_hsa_circ_106760,RMVar_hsa_circ_165742,RMVar_hsa_circ_165743,RMVar_hsa_circ_373117,RMVar_hsa_circ_86572,RMVar_hsa_circ_165744,RMVar_hsa_circ_165745,RMVar_hsa_circ_295503,RMVar_hsa_circ_120359,RMVar_hsa_circ_74712,RMVar_hsa_circ_23697,RMVar_hsa_circ_165749,RMVar_hsa_circ_165750,RMVar_hsa_circ_165748,RMVar_hsa_circ_294611,RMVar_hsa_circ_122682,RMVar_hsa_circ_88463,RMVar_hsa_circ_165752,RMVar_hsa_circ_165753,RMVar_hsa_circ_266145,RMVar_hsa_circ_373676,RMVar_hsa_circ_165754,RMVar_hsa_circ_300520,RMVar_hsa_circ_265529,RMVar_hsa_circ_306306,RMVar_hsa_circ_165756,RMVar_hsa_circ_165755,RMVar_hsa_circ_313334,RMVar_hsa_circ_165759,RMVar_hsa_circ_288238,RMVar_hsa_circ_165758 25576 RMVar_ID_25576 Human_SNP_ID_549973845 A-to-I Human chr14 - 31366236 31366236 31366236 ACTATTTCAGTCTGTCGCCCGGGATTGAGTGCAGTGGCGCAGTCATAGCTCACCATATCCTCAAA ACTATTTCAGTCTGTCGCCCGGGATTGAGTGCTGTGGCGCAGTCATAGCTCACCATATCCTCAAA T A AL139353.1,HEATR5A Ensembl:ENSG00000203546,Ensembl:ENSG00000129493 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1376957624 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12315516 RMVar_hsa_circ_663,RMVar_hsa_circ_119850,RMVar_hsa_circ_95747,RMVar_hsa_circ_165680,RMVar_hsa_circ_165681,RMVar_hsa_circ_278379,RMVar_hsa_circ_343730,RMVar_hsa_circ_336399,RMVar_hsa_circ_116723,RMVar_hsa_circ_99941,RMVar_hsa_circ_165686,RMVar_hsa_circ_165688,RMVar_hsa_circ_165687,RMVar_hsa_circ_78668,RMVar_hsa_circ_165698,RMVar_hsa_circ_90560,RMVar_hsa_circ_2808,RMVar_hsa_circ_165702,RMVar_hsa_circ_165703,RMVar_hsa_circ_118407,RMVar_hsa_circ_268993,RMVar_hsa_circ_165714,RMVar_hsa_circ_339111,RMVar_hsa_circ_94685,RMVar_hsa_circ_165716,RMVar_hsa_circ_165715,RMVar_hsa_circ_102824,RMVar_hsa_circ_165722,RMVar_hsa_circ_102772,RMVar_hsa_circ_165723,RMVar_hsa_circ_327937,RMVar_hsa_circ_42893,RMVar_hsa_circ_90831,RMVar_hsa_circ_165731,RMVar_hsa_circ_311548,RMVar_hsa_circ_265515,RMVar_hsa_circ_318504,RMVar_hsa_circ_165732,RMVar_hsa_circ_107730,RMVar_hsa_circ_165734,RMVar_hsa_circ_61180,RMVar_hsa_circ_165735,RMVar_hsa_circ_165733,RMVar_hsa_circ_286417,RMVar_hsa_circ_111300,RMVar_hsa_circ_42119,RMVar_hsa_circ_15725,RMVar_hsa_circ_106760,RMVar_hsa_circ_165742,RMVar_hsa_circ_165743,RMVar_hsa_circ_373117,RMVar_hsa_circ_86572,RMVar_hsa_circ_165744,RMVar_hsa_circ_165745,RMVar_hsa_circ_295503,RMVar_hsa_circ_120359,RMVar_hsa_circ_74712,RMVar_hsa_circ_23697,RMVar_hsa_circ_165749,RMVar_hsa_circ_165750,RMVar_hsa_circ_165748,RMVar_hsa_circ_294611,RMVar_hsa_circ_122682,RMVar_hsa_circ_88463,RMVar_hsa_circ_165752,RMVar_hsa_circ_165753,RMVar_hsa_circ_266145,RMVar_hsa_circ_373676,RMVar_hsa_circ_165754,RMVar_hsa_circ_300520,RMVar_hsa_circ_265529,RMVar_hsa_circ_306306,RMVar_hsa_circ_165756,RMVar_hsa_circ_165755,RMVar_hsa_circ_313334,RMVar_hsa_circ_165759,RMVar_hsa_circ_288238,RMVar_hsa_circ_165758 25577 RMVar_ID_25577 Human_SNP_ID_549976815 A-to-I Human chr14 - 31378454 31378454 31378454 ATTAAAGAGATTTATTGGACTAGATCAAGTTTAGCTTCAAGGAGCCAAATTTGGCCTACTACCAA ATTAAAGAGATTTATTGGACTAGATCAAGTTTGGCTTCAAGGAGCCAAATTTGGCCTACTACCAA T C AL139353.1,HEATR5A Ensembl:ENSG00000203546,Ensembl:ENSG00000129493 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404440121 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_663,RMVar_hsa_circ_119850,RMVar_hsa_circ_165681,RMVar_hsa_circ_336399,RMVar_hsa_circ_116723,RMVar_hsa_circ_99941,RMVar_hsa_circ_165686,RMVar_hsa_circ_165687,RMVar_hsa_circ_165703,RMVar_hsa_circ_118407,RMVar_hsa_circ_268993,RMVar_hsa_circ_165714,RMVar_hsa_circ_94685,RMVar_hsa_circ_165715,RMVar_hsa_circ_102772,RMVar_hsa_circ_42893,RMVar_hsa_circ_265515,RMVar_hsa_circ_107730,RMVar_hsa_circ_165734,RMVar_hsa_circ_61180,RMVar_hsa_circ_165733,RMVar_hsa_circ_111300,RMVar_hsa_circ_42119,RMVar_hsa_circ_15725,RMVar_hsa_circ_106760,RMVar_hsa_circ_165743,RMVar_hsa_circ_86572,RMVar_hsa_circ_165744,RMVar_hsa_circ_120359,RMVar_hsa_circ_74712,RMVar_hsa_circ_165749,RMVar_hsa_circ_165750,RMVar_hsa_circ_294611,RMVar_hsa_circ_122682,RMVar_hsa_circ_165752,RMVar_hsa_circ_165753,RMVar_hsa_circ_266145,RMVar_hsa_circ_373676,RMVar_hsa_circ_265529,RMVar_hsa_circ_11220,RMVar_hsa_circ_165755,RMVar_hsa_circ_165759,RMVar_hsa_circ_288238,RMVar_hsa_circ_333168,RMVar_hsa_circ_368142,RMVar_hsa_circ_71774,RMVar_hsa_circ_303460 25578 RMVar_ID_25578 Human_SNP_ID_549977298 A-to-I Human chr14 - 31379863 31379863 31379863 GCCTTGACCTCCTGGGCCCAAGTGATCCTCCTACCTAAGCCTCCCAAGTAGCTGGGACCATAGGC GCCTTGACCTCCTGGGCCCAAGTGATCCTCCTCCCTAAGCCTCCCAAGTAGCTGGGACCATAGGC T G AL139353.1,HEATR5A Ensembl:ENSG00000203546,Ensembl:ENSG00000129493 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1377814954 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_663,RMVar_hsa_circ_119850,RMVar_hsa_circ_165681,RMVar_hsa_circ_336399,RMVar_hsa_circ_116723,RMVar_hsa_circ_99941,RMVar_hsa_circ_165686,RMVar_hsa_circ_165687,RMVar_hsa_circ_165703,RMVar_hsa_circ_118407,RMVar_hsa_circ_268993,RMVar_hsa_circ_165714,RMVar_hsa_circ_94685,RMVar_hsa_circ_165715,RMVar_hsa_circ_102772,RMVar_hsa_circ_42893,RMVar_hsa_circ_265515,RMVar_hsa_circ_107730,RMVar_hsa_circ_165734,RMVar_hsa_circ_61180,RMVar_hsa_circ_165733,RMVar_hsa_circ_111300,RMVar_hsa_circ_42119,RMVar_hsa_circ_15725,RMVar_hsa_circ_106760,RMVar_hsa_circ_165743,RMVar_hsa_circ_86572,RMVar_hsa_circ_165744,RMVar_hsa_circ_120359,RMVar_hsa_circ_74712,RMVar_hsa_circ_165749,RMVar_hsa_circ_165750,RMVar_hsa_circ_294611,RMVar_hsa_circ_122682,RMVar_hsa_circ_165752,RMVar_hsa_circ_165753,RMVar_hsa_circ_266145,RMVar_hsa_circ_373676,RMVar_hsa_circ_265529,RMVar_hsa_circ_11220,RMVar_hsa_circ_165755,RMVar_hsa_circ_165759,RMVar_hsa_circ_288238,RMVar_hsa_circ_333168,RMVar_hsa_circ_368142,RMVar_hsa_circ_71774,RMVar_hsa_circ_303460 25579 RMVar_ID_25579 Human_SNP_ID_549981658 A-to-I Human chr14 - 31397824 31397824 31397824 TGGAAGACCCTGTCTCTACAAAAACATAAATTAGTTGGGGTATGGTGGTGAACACCTGTAGTTCT TGGAAGACCCTGTCTCTACAAAAACATAAATTGGTTGGGGTATGGTGGTGAACACCTGTAGTTCT T C AL139353.1,HEATR5A Ensembl:ENSG00000203546,Ensembl:ENSG00000129493 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1452887236 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119850,RMVar_hsa_circ_165681,RMVar_hsa_circ_99941,RMVar_hsa_circ_165686,RMVar_hsa_circ_111300,RMVar_hsa_circ_21928,RMVar_hsa_circ_106760,RMVar_hsa_circ_165743,RMVar_hsa_circ_86572,RMVar_hsa_circ_165744,RMVar_hsa_circ_165750,RMVar_hsa_circ_373676,RMVar_hsa_circ_165755,RMVar_hsa_circ_55635,RMVar_hsa_circ_33475,RMVar_hsa_circ_43127,RMVar_hsa_circ_61300,RMVar_hsa_circ_360502,RMVar_hsa_circ_374470,RMVar_hsa_circ_321299,RMVar_hsa_circ_165769,RMVar_hsa_circ_26463 25580 RMVar_ID_25580 Human_SNP_ID_549992149 A-to-I Human chr14 - 31440803 31440803 31440803 ATGTTCCCCATCCTGAGACATGGGGTTTCACCATGTTGACCAGGCTGGTCTCGAACTCCGGACCT ATGTTCCCCATCCTGAGACATGGGGTTTCACCGTGTTGACCAGGCTGGTCTCGAACTCCGGACCT T C AL139353.1 Ensembl:ENSG00000203546 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs919689517 Functional Loss SNV dbSNP153 33..33 33 - - - 25581 RMVar_ID_25581 Human_SNP_ID_549993609 A-to-I Human chr14 - 31447255 31447255 31447255 TATAGGGCCAAATGTGGTGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCCGAGGTGGGAGGA TATAGGGCCAAATGTGGTGGCTCATGCCTATAGTCCCAGCACTTTGGGAGGCCGAGGTGGGAGGA T C AL139353.1,DTD2 Ensembl:ENSG00000203546,Ensembl:ENSG00000129480 Protein coding,Protein coding intron,3'UTR GSE47997;GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,29129909,31158229,31158229,32596459 RNA-Seq:(High) rs986694174 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_165771,RMVar_hsa_circ_95776 25582 RMVar_ID_25582 Human_SNP_ID_549993610 A-to-I Human chr14 - 31447258 31447258 31447258 TAATATAGGGCCAAATGTGGTGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCCGAGGTGGGA TAATATAGGGCCAAATGTGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGA T C AL139353.1,DTD2 Ensembl:ENSG00000203546,Ensembl:ENSG00000129480 Protein coding,Protein coding intron,3'UTR GSE47997;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,29129909,29796672,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs912509125 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_165771,RMVar_hsa_circ_95776 25583 RMVar_ID_25583 Human_SNP_ID_549993712 A-to-I Human chr14 - 31447721 31447721 31447721 CACCTCCTGGATTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCGCATG CACCTCCTGGATTCAAGCGATTCTCCTGCCTCTGCCTCCCAAGTAGCTGGGATTACAGGCGCATG T A AL139353.1,DTD2 Ensembl:ENSG00000203546,Ensembl:ENSG00000129480 Protein coding,Protein coding intron,3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,31158229,32596459,32596459 RNA-Seq:(High) rs1165297598 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_165771,RMVar_hsa_circ_95776 25584 RMVar_ID_25584 Human_SNP_ID_550067054 A-to-I Human chr14 + 31746947 31746947 31746947 TAAAAATTAGCCAGATGTGGTGGCTTGTGCCTATAGTTCCAGCTACTTGAGGGGCTGAGGCCAGA TAAAAATTAGCCAGATGTGGTGGCTTGTGCCTGTAGTTCCAGCTACTTGAGGGGCTGAGGCCAGA A G NUBPL Ensembl:ENSG00000151413 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1374906332 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_287054,RMVar_hsa_circ_301487 25585 RMVar_ID_25585 Human_SNP_ID_550079921 A-to-I Human chr14 + 31799268 31799265 31799268 CACAAAAAAATCCTTTTTTATAGTGTACATGTAGTTTCTAGAAAATACTATACATTTGGATGGAA CACAAAAAAATCCTTTTTTATAGTGTACAT___GTTTCTAGAAAATACTATACATTTGGATGGAA TGTA T NUBPL Ensembl:ENSG00000151413 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049758527 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_9763495 RMVar_hsa_circ_275525,RMVar_hsa_circ_165782 25586 RMVar_ID_25586 Human_SNP_ID_550079923 A-to-I Human chr14 + 31799268 31799268 31799268 CACAAAAAAATCCTTTTTTATAGTGTACATGTAGTTTCTAGAAAATACTATACATTTGGATGGAA CACAAAAAAATCCTTTTTTATAGTGTACATGTCGTTTCTAGAAAATACTATACATTTGGATGGAA A C NUBPL Ensembl:ENSG00000151413 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs907014631 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9763495 RMVar_hsa_circ_275525,RMVar_hsa_circ_165782 25587 RMVar_ID_25587 Human_SNP_ID_550079939 A-to-I Human chr14 + 31799320 31799320 31799320 CATTTGGATGGAATATTTACATTCATTATCTTATTTGATCCTTACAAGTCTGTGGAGTTAAGTTC CATTTGGATGGAATATTTACATTCATTATCTTGTTTGATCCTTACAAGTCTGTGGAGTTAAGTTC A G NUBPL Ensembl:ENSG00000151413 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956818515 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_275525,RMVar_hsa_circ_165782 25588 RMVar_ID_25588 Human_SNP_ID_550079940 A-to-I Human chr14 + 31799320 31799320 31799320 CATTTGGATGGAATATTTACATTCATTATCTTATTTGATCCTTACAAGTCTGTGGAGTTAAGTTC CATTTGGATGGAATATTTACATTCATTATCTTTTTTGATCCTTACAAGTCTGTGGAGTTAAGTTC A T NUBPL Ensembl:ENSG00000151413 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956818515 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_275525,RMVar_hsa_circ_165782 25589 RMVar_ID_25589 Human_SNP_ID_550086030 A-to-I Human chr14 + 31819879 31819852 31819880 CAGAGAATTCTTGGCCAGGCGTGGTGGCTCACACCTGTTATCCCAGCACTTTAGGAGGCTGAGGT CAGAGA____________________________CTGTTATCCCAGCACTTTAGGAGGCTGAGGT AATTCTTGGCCAGGCGTGGTGGCTCACAC A NUBPL Ensembl:ENSG00000151413 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404244199 Functional Loss DEL dbSNP153 7..34 33 - - - RMVar_hsa_circ_275525,RMVar_hsa_circ_165782 25590 RMVar_ID_25590 Human_SNP_ID_550086041 A-to-I Human chr14 + 31819879 31819879 31819879 CAGAGAATTCTTGGCCAGGCGTGGTGGCTCACACCTGTTATCCCAGCACTTTAGGAGGCTGAGGT CAGAGAATTCTTGGCCAGGCGTGGTGGCTCACGCCTGTTATCCCAGCACTTTAGGAGGCTGAGGT A G NUBPL Ensembl:ENSG00000151413 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs923854423 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_275525,RMVar_hsa_circ_165782 25591 RMVar_ID_25591 Human_SNP_ID_550087733 A-to-I Human chr14 + 31826321 31826321 31826321 TTTTGTATTTTTAGTAGTTACAGGGTTTCACCATGTTAGCCAGGCTGGTCTTGAACTCCTGACCC TTTTGTATTTTTAGTAGTTACAGGGTTTCACCGTGTTAGCCAGGCTGGTCTTGAACTCCTGACCC A G NUBPL Ensembl:ENSG00000151413 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1346421732 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_275525,RMVar_hsa_circ_165782 25592 RMVar_ID_25592 Human_SNP_ID_550089391 A-to-I Human chr14 + 31833112 31833112 31833112 ATTTGGGGCTGGGCGTGGTGGCTCATGCCTGTAATCCCAGCACTTTGTGAGGCCGAGGCAGGAGT ATTTGGGGCTGGGCGTGGTGGCTCATGCCTGTGATCCCAGCACTTTGTGAGGCCGAGGCAGGAGT A G NUBPL Ensembl:ENSG00000151413 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1180103373 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22553,RMVar_hsa_circ_39206 25593 RMVar_ID_25593 Human_SNP_ID_550154771 A-to-I Human chr14 + 32100279 32100279 32100279 CTGGAGTGCAGTGGTACCATCGAGCTCACTGCAGTCTCAGACCCCTGGGTTCAAGTGATCTTCTC CTGGAGTGCAGTGGTACCATCGAGCTCACTGCGGTCTCAGACCCCTGGGTTCAAGTGATCTTCTC A G ARHGAP5 Ensembl:ENSG00000100852 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1021349427 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6341127 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 25594 RMVar_ID_25594 Human_SNP_ID_550168437 A-to-I Human chr14 + 32153653 32153653 32153653 CACCACCACACCCAGCTAAATTTAGTATTTTTAGTAGAGACAGGGTTTCATCATGTTGGCCAAGA CACCACCACACCCAGCTAAATTTAGTATTTTTGGTAGAGACAGGGTTTCATCATGTTGGCCAAGA A G ARHGAP5 Ensembl:ENSG00000100852 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1248264406 Functional Loss SNV dbSNP153 33..33 33 - - - 25595 RMVar_ID_25595 Human_SNP_ID_550196773 A-to-I Human chr14 - 32268600 32268600 32268600 CTATGTCAGATAAAGAATCACCCAGGCCAGACACAATGGCTCATGCTTGTGATCCCAACACTTTG CTATGTCAGATAAAGAATCACCCAGGCCAGACCCAATGGCTCATGCTTGTGATCCCAACACTTTG T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs983739680 Functional Loss SNV dbSNP153 33..33 33 - - - 25596 RMVar_ID_25596 Human_SNP_ID_550279001 A-to-I Human chr14 + 32614937 32614937 32614937 TCACACCTGTTATCCCAGCACTTTGGGAGGCCAAGGCGGGCAGATCATGAGGTCAAGAGATCGAG TCACACCTGTTATCCCAGCACTTTGGGAGGCCGAGGCGGGCAGATCATGAGGTCAAGAGATCGAG A G AKAP6 Ensembl:ENSG00000151320 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs184837440 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_120341 RMVar_hsa_circ_13522,RMVar_hsa_circ_104182,RMVar_hsa_circ_80361,RMVar_hsa_circ_165811,RMVar_hsa_circ_28366,RMVar_hsa_circ_165814 25597 RMVar_ID_25597 Human_SNP_ID_550279017 A-to-I Human chr14 + 32614973 32614973 32614973 CGGGCAGATCATGAGGTCAAGAGATCGAGACCATCCTGGCCAACATGGTGAAACCCCGTCTCTAC CGGGCAGATCATGAGGTCAAGAGATCGAGACCGTCCTGGCCAACATGGTGAAACCCCGTCTCTAC A G AKAP6 Ensembl:ENSG00000151320 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1275807676 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_120341 RMVar_hsa_circ_13522,RMVar_hsa_circ_104182,RMVar_hsa_circ_80361,RMVar_hsa_circ_165811,RMVar_hsa_circ_28366,RMVar_hsa_circ_165814 25598 RMVar_ID_25598 Human_SNP_ID_550279032 A-to-I Human chr14 + 32615010 32615010 32615010 GGCCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCTGGGCGTGGTGGTGCACA GGCCAACATGGTGAAACCCCGTCTCTACTAAATATACAAAAATTAGCTGGGCGTGGTGGTGCACA A T AKAP6 Ensembl:ENSG00000151320 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1361147834 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_120341 RMVar_hsa_circ_13522,RMVar_hsa_circ_104182,RMVar_hsa_circ_80361,RMVar_hsa_circ_165811,RMVar_hsa_circ_28366,RMVar_hsa_circ_165814 25599 RMVar_ID_25599 Human_SNP_ID_550316614 A-to-I Human chr14 + 32775633 32775633 32775633 TTTTATTTTACTTTTTGTAGAGACATGGTCTCACTATGTTGCCCAGGCTGGTCTCAAATTCTTGG TTTTATTTTACTTTTTGTAGAGACATGGTCTCGCTATGTTGCCCAGGCTGGTCTCAAATTCTTGG A G AKAP6 Ensembl:ENSG00000151320 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1024754229 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36897 25600 RMVar_ID_25600 Human_SNP_ID_550317412 A-to-I Human chr14 + 32778827 32778827 32778827 CCTTGGCCTCCCACAGTGCTGGGATTACAGGCATGAGTCGCCATGCCTAGCTTATAACTCTTTAA CCTTGGCCTCCCACAGTGCTGGGATTACAGGCGTGAGTCGCCATGCCTAGCTTATAACTCTTTAA A G AKAP6 Ensembl:ENSG00000151320 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1404312825 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36897 25601 RMVar_ID_25601 Human_SNP_ID_550359882 A-to-I Human chr14 + 32939500 32939500 32939500 GCCGCGAGCCCGCGGGGACCTCGTCTGGGCGCAGCGCTCGCCCGGGGCCCCGCGCATTGTCCCCG GCCGCGAGCCCGCGGGGACCTCGTCTGGGCGCCGCGCTCGCCCGGGGCCCCGCGCATTGTCCCCG A C NPAS3 Ensembl:ENSG00000151322 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1248499005 Functional Loss SNV dbSNP153 33..33 33 - - - 25602 RMVar_ID_25602 Human_SNP_ID_550730008 A-to-I Human chr14 - 34435251 34435251 34435251 TGGGGATGGCACTATACACAGGATACGTCTTCATGCCCCAGCACATCATGGCGATATTGCACTAC TGGGGATGGCACTATACACAGGATACGTCTTCGTGCCCCAGCACATCATGGCGATATTGCACTAC T C EGLN3,SPTSSA Ensembl:ENSG00000129521,Ensembl:ENSG00000165389 Protein coding,Protein coding intron,CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs17851911 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_444899,Human_RBP_ID_1492954,Human_RBP_ID_17847631,Human_RBP_ID_22439167,Human_RBP_ID_26808019 Human_Splice_Rec_1506064 Human_miRNA_ID_2685115 RMVar_hsa_circ_76087,RMVar_hsa_circ_165852 25603 RMVar_ID_25603 Human_SNP_ID_550730589 A-to-I Human chr14 - 34438021 34438021 34438021 AGGTGGGAGGATTGCTTGTCCCCAGGAGTTCAAGACCAGCCTGAGCAACATAGGGAGACCCCATC AGGTGGGAGGATTGCTTGTCCCCAGGAGTTCACGACCAGCCTGAGCAACATAGGGAGACCCCATC T G EGLN3,SPTSSA Ensembl:ENSG00000129521,Ensembl:ENSG00000165389 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs908955336 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76087,RMVar_hsa_circ_165852 25604 RMVar_ID_25604 Human_SNP_ID_550730609 A-to-I Human chr14 - 34438082 34438082 34438082 AGGGGATTGGCCAGCTCGGCGTGGTGGCTCACACCTGTAATCTCAGCACTTTGGGGGGCTGAGGT AGGGGATTGGCCAGCTCGGCGTGGTGGCTCACTCCTGTAATCTCAGCACTTTGGGGGGCTGAGGT T A EGLN3,SPTSSA Ensembl:ENSG00000129521,Ensembl:ENSG00000165389 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1050313855 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76087,RMVar_hsa_circ_165852 25605 RMVar_ID_25605 Human_SNP_ID_550732413 A-to-I Human chr14 - 34444524 34444524 34444524 TGGTCTTGAACTGTTGACCTCGGGATCCACCCACGTCGGCCTCCCAAAGTGCTGGGATTACAGGT TGGTCTTGAACTGTTGACCTCGGGATCCACCCTCGTCGGCCTCCCAAAGTGCTGGGATTACAGGT T A EGLN3,SPTSSA Ensembl:ENSG00000129521,Ensembl:ENSG00000165389 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs371003220 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12318032,Human_RBP_ID_25094551 RMVar_hsa_circ_76087,RMVar_hsa_circ_165852 25606 RMVar_ID_25606 Human_SNP_ID_550732438 A-to-I Human chr14 - 34444586 34444586 34444586 CACCACGCCCAGCTAATTTTTGTATTTTCAGTAGAGACAGGGTTTCACTATGTTGGCCAGGATGG CACCACGCCCAGCTAATTTTTGTATTTTCAGTGGAGACAGGGTTTCACTATGTTGGCCAGGATGG T C EGLN3,SPTSSA Ensembl:ENSG00000129521,Ensembl:ENSG00000165389 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1312680766 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76087,RMVar_hsa_circ_165852 25607 RMVar_ID_25607 Human_SNP_ID_550732474 A-to-I Human chr14 - 34444750 34444747 34444751 ATGACGACTCTTAGCAATTTTTTTTTTTTTTGAGGCAGAGTCTTGCCCTGTGGCCCAGGCTGGAG ATGACGACTCTTAGCAATTTTTTTTTTTTTT____CAGAGTCTTGCCCTGTGGCCCAGGCTGGAG GCCTC G EGLN3,SPTSSA Ensembl:ENSG00000129521,Ensembl:ENSG00000165389 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1453466064 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_12318039 RMVar_hsa_circ_76087,RMVar_hsa_circ_165852 25608 RMVar_ID_25608 Human_SNP_ID_550733560 A-to-I Human chr14 - 34449273 34449273 34449273 TTCCTGCTTCATCCTCCCGAGTATCTGGGACTACAGGCATATATCACCATGCCTGGCTAATTGTT TTCCTGCTTCATCCTCCCGAGTATCTGGGACTGCAGGCATATATCACCATGCCTGGCTAATTGTT T C EGLN3,SPTSSA Ensembl:ENSG00000129521,Ensembl:ENSG00000165389 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs574083982 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76087,RMVar_hsa_circ_165852 25609 RMVar_ID_25609 Human_SNP_ID_550733569 A-to-I Human chr14 - 34449342 34449342 34449342 CATCCAGGCTAGAGTGCAGTAGTGTTATTTCAACTCACAGCAACCTCTGCTTTCTGGGCTCAAGT CATCCAGGCTAGAGTGCAGTAGTGTTATTTCAGCTCACAGCAACCTCTGCTTTCTGGGCTCAAGT T C EGLN3,SPTSSA Ensembl:ENSG00000129521,Ensembl:ENSG00000165389 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1000847046 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76087,RMVar_hsa_circ_165852 25610 RMVar_ID_25610 Human_SNP_ID_550733677 A-to-I Human chr14 - 34449641 34449641 34449641 AAAATCAGCTGGGCGTGGTGGCACGTGCCTGTAATTCTAGCTACTCGGGAGACTGAGGCAGAAGA AAAATCAGCTGGGCGTGGTGGCACGTGCCTGTGATTCTAGCTACTCGGGAGACTGAGGCAGAAGA T C EGLN3,SPTSSA Ensembl:ENSG00000129521,Ensembl:ENSG00000165389 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910774697 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76087,RMVar_hsa_circ_165852 25611 RMVar_ID_25611 Human_SNP_ID_550733719 A-to-I Human chr14 - 34449778 34449778 34449778 AATGCCTAGGTCGGGTGTGGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGACTGAGGTGGGC AATGCCTAGGTCGGGTGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGACTGAGGTGGGC T C EGLN3,SPTSSA Ensembl:ENSG00000129521,Ensembl:ENSG00000165389 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1276960317 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76087,RMVar_hsa_circ_165852 25612 RMVar_ID_25612 Human_SNP_ID_550734824 A-to-I Human chr14 - 34453921 34453921 34453921 CCTGCCTCAGCTTTCCAAAGTGCTCGGATTACAGGTGTGAACCATCGGACCTGGCCTCTTTTTTT CCTGCCTCAGCTTTCCAAAGTGCTCGGATTACGGGTGTGAACCATCGGACCTGGCCTCTTTTTTT T C EGLN3,SPTSSA Ensembl:ENSG00000129521,Ensembl:ENSG00000165389 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1566426106 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76087,RMVar_hsa_circ_165852 25613 RMVar_ID_25613 Human_SNP_ID_550734839 A-to-I Human chr14 - 34454017 34454017 34454017 CACCACCATGCCTGATTAATTTTTAAATTTTTAGTAGAGACAGGGTCTCACTAGGTTGCCTAGGT CACCACCATGCCTGATTAATTTTTAAATTTTTGGTAGAGACAGGGTCTCACTAGGTTGCCTAGGT T C EGLN3,SPTSSA Ensembl:ENSG00000129521,Ensembl:ENSG00000165389 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1471599325 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12318412 RMVar_hsa_circ_76087,RMVar_hsa_circ_165852 25614 RMVar_ID_25614 Human_SNP_ID_550735019 A-to-I Human chr14 - 34454924 34454924 34454924 TGCCACCACACCCGGCTGATTTTTGTATTTTTAGTAGAGAAGGGGATTTACTATGTTGGCCAGCC TGCCACCACACCCGGCTGATTTTTGTATTTTTGGTAGAGAAGGGGATTTACTATGTTGGCCAGCC T C EGLN3,SPTSSA Ensembl:ENSG00000129521,Ensembl:ENSG00000165389 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1399783663 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12318470 RMVar_hsa_circ_76087,RMVar_hsa_circ_165852 25615 RMVar_ID_25615 Human_SNP_ID_550735303 A-to-I Human chr14 - 34455810 34455810 34455810 CTCATTCCTCAGCCTCCTGAATAGCTAGGATTACAGTTGCACGCCACCATGCCCAGGTAATTTTT CTCATTCCTCAGCCTCCTGAATAGCTAGGATTGCAGTTGCACGCCACCATGCCCAGGTAATTTTT T C EGLN3,SPTSSA Ensembl:ENSG00000129521,Ensembl:ENSG00000165389 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1406709948 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12318501 RMVar_hsa_circ_76087,RMVar_hsa_circ_165852 25616 RMVar_ID_25616 Human_SNP_ID_550735392 A-to-I Human chr14 - 34456133 34456133 34456133 TTTTTTTAGTAGAGACGGGGTTTCACCATGTTAGCCGGATGGTCTCGATCTCCTGACCTCGTGAT TTTTTTTAGTAGAGACGGGGTTTCACCATGTTCGCCGGATGGTCTCGATCTCCTGACCTCGTGAT T G EGLN3,SPTSSA Ensembl:ENSG00000129521,Ensembl:ENSG00000165389 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1007150331 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76087,RMVar_hsa_circ_165852 25617 RMVar_ID_25617 Human_SNP_ID_550735547 A-to-I Human chr14 - 34456777 34456777 34456777 GTTCCGCCTTGCCCTCCCGAGTAGCTGGGACTACAGGTGTGTGCCACCACGCCCGGCTAATTTTT GTTCCGCCTTGCCCTCCCGAGTAGCTGGGACTGCAGGTGTGTGCCACCACGCCCGGCTAATTTTT T C EGLN3,SPTSSA Ensembl:ENSG00000129521,Ensembl:ENSG00000165389 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1281227168 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76087,RMVar_hsa_circ_165852 25618 RMVar_ID_25618 Human_SNP_ID_550735562 A-to-I Human chr14 - 34456836 34456836 34456836 GGAGTGCAGTGGCGCGATCTTGGCTCGCTGCAACCTCTGCCTCCTGGATTCAAGCAATTGTTCCG GGAGTGCAGTGGCGCGATCTTGGCTCGCTGCAGCCTCTGCCTCCTGGATTCAAGCAATTGTTCCG T C EGLN3,SPTSSA Ensembl:ENSG00000129521,Ensembl:ENSG00000165389 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1446589732 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12464767 RMVar_hsa_circ_76087,RMVar_hsa_circ_165852 25619 RMVar_ID_25619 Human_SNP_ID_550735663 A-to-I Human chr14 - 34457135 34457135 34457135 TGTCTCTACTAAAAATAAAAAATTAGTGGGGCATGGTGGCTGGCGCCTGTAGTCCCAGCTACATG TGTCTCTACTAAAAATAAAAAATTAGTGGGGCGTGGTGGCTGGCGCCTGTAGTCCCAGCTACATG T C EGLN3,SPTSSA Ensembl:ENSG00000129521,Ensembl:ENSG00000165389 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1260808910 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76087,RMVar_hsa_circ_165852 25620 RMVar_ID_25620 Human_SNP_ID_550735674 A-to-I Human chr14 - 34457153 34457152 34457153 GCCAGCATGGTGAATTCTTGTCTCTACTAAAAATAAAAAATTAGTGGGGCATGGTGGCTGGCGCC GCCAGCATGGTGAATTCTTGTCTCTACTAAAA_TAAAAAATTAGTGGGGCATGGTGGCTGGCGCC AT A EGLN3,SPTSSA Ensembl:ENSG00000129521,Ensembl:ENSG00000165389 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1566427041 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_76087,RMVar_hsa_circ_165852 25621 RMVar_ID_25621 Human_SNP_ID_550735675 A-to-I Human chr14 - 34457157 34457157 34457157 CTCGGCCAGCATGGTGAATTCTTGTCTCTACTAAAAATAAAAAATTAGTGGGGCATGGTGGCTGG CTCGGCCAGCATGGTGAATTCTTGTCTCTACTGAAAATAAAAAATTAGTGGGGCATGGTGGCTGG T C EGLN3,SPTSSA Ensembl:ENSG00000129521,Ensembl:ENSG00000165389 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1239829845 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76087,RMVar_hsa_circ_165852 25622 RMVar_ID_25622 Human_SNP_ID_550735682 A-to-I Human chr14 - 34457196 34457196 34457196 AGGTGGCTGGATCACCTGAGGTCAAGAGTTCAAGGCCAGCTCGGCCAGCATGGTGAATTCTTGTC AGGTGGCTGGATCACCTGAGGTCAAGAGTTCAGGGCCAGCTCGGCCAGCATGGTGAATTCTTGTC T C EGLN3,SPTSSA Ensembl:ENSG00000129521,Ensembl:ENSG00000165389 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs144994815 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76087,RMVar_hsa_circ_165852 25623 RMVar_ID_25623 Human_SNP_ID_550735683 A-to-I Human chr14 - 34457196 34457196 34457196 AGGTGGCTGGATCACCTGAGGTCAAGAGTTCAAGGCCAGCTCGGCCAGCATGGTGAATTCTTGTC AGGTGGCTGGATCACCTGAGGTCAAGAGTTCACGGCCAGCTCGGCCAGCATGGTGAATTCTTGTC T G EGLN3,SPTSSA Ensembl:ENSG00000129521,Ensembl:ENSG00000165389 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs144994815 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76087,RMVar_hsa_circ_165852 25624 RMVar_ID_25624 Human_SNP_ID_550735840 A-to-I Human chr14 - 34457850 34457850 34457850 CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCCGTGCCACCATGCCCAGCTAAATTTTT CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTGCAGGCCGTGCCACCATGCCCAGCTAAATTTTT T C EGLN3,SPTSSA Ensembl:ENSG00000129521,Ensembl:ENSG00000165389 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1356079988 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76087,RMVar_hsa_circ_165852 25625 RMVar_ID_25625 Human_SNP_ID_550735848 A-to-I Human chr14 - 34457890 34457890 34457890 TCGGTTCACTGCAGCCTCTGCCTCTGGGATTCAGGCGATTCTCCTGCCTCAGCCTCCCAAGTAGC TCGGTTCACTGCAGCCTCTGCCTCTGGGATTCGGGCGATTCTCCTGCCTCAGCCTCCCAAGTAGC T C EGLN3,SPTSSA Ensembl:ENSG00000129521,Ensembl:ENSG00000165389 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991272298 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2411811,Human_RBP_ID_12318576 RMVar_hsa_circ_76087,RMVar_hsa_circ_165852 25626 RMVar_ID_25626 Human_SNP_ID_550735851 A-to-I Human chr14 - 34457910 34457910 34457910 TGGAGTGCAGTGGTGCGATCTCGGTTCACTGCAGCCTCTGCCTCTGGGATTCAGGCGATTCTCCT TGGAGTGCAGTGGTGCGATCTCGGTTCACTGCGGCCTCTGCCTCTGGGATTCAGGCGATTCTCCT T C EGLN3,SPTSSA Ensembl:ENSG00000129521,Ensembl:ENSG00000165389 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs915745301 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2411811,Human_RBP_ID_6342121,Human_RBP_ID_12318577 RMVar_hsa_circ_76087,RMVar_hsa_circ_165852 25627 RMVar_ID_25627 Human_SNP_ID_550735993 A-to-I Human chr14 - 34458335 34458335 34458335 TACTAAAAATGCAAATATTAGCCGGGTGTAGTAGTGTACGCCAGCTACTTTGGTGGCTGAGGCAC TACTAAAAATGCAAATATTAGCCGGGTGTAGTTGTGTACGCCAGCTACTTTGGTGGCTGAGGCAC T A EGLN3,SPTSSA Ensembl:ENSG00000129521,Ensembl:ENSG00000165389 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs887467577 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12318602 RMVar_hsa_circ_76087,RMVar_hsa_circ_165852 25628 RMVar_ID_25628 Human_SNP_ID_550736001 A-to-I Human chr14 - 34458360 34458360 34458360 AGAAAACATGGTGAAACTCAGTCTGTACTAAAAATGCAAATATTAGCCGGGTGTAGTAGTGTACG AGAAAACATGGTGAAACTCAGTCTGTACTAAAGATGCAAATATTAGCCGGGTGTAGTAGTGTACG T C EGLN3,SPTSSA Ensembl:ENSG00000129521,Ensembl:ENSG00000165389 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1162812264 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9764054 RMVar_hsa_circ_76087,RMVar_hsa_circ_165852 25629 RMVar_ID_25629 Human_SNP_ID_550736032 A-to-I Human chr14 - 34458470 34458470 34458470 AAAAAGAAAGTCGATCTTAGGCCTGGCGCGGTAGCTCACACCTGTAATCCCAGCACTCTGGGAGG AAAAAGAAAGTCGATCTTAGGCCTGGCGCGGTTGCTCACACCTGTAATCCCAGCACTCTGGGAGG T A EGLN3,SPTSSA Ensembl:ENSG00000129521,Ensembl:ENSG00000165389 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1266637686 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12318608 RMVar_hsa_circ_76087,RMVar_hsa_circ_165852 25630 RMVar_ID_25630 Human_SNP_ID_550736198 A-to-I Human chr14 - 34458967 34458967 34458967 CCGGGAGGCGGAGGTTGCAGTGAGCCGAGATCACGCCACTGCACTCTAGCCTCAGTGACAGAGTG CCGGGAGGCGGAGGTTGCAGTGAGCCGAGATCGCGCCACTGCACTCTAGCCTCAGTGACAGAGTG T C EGLN3,SPTSSA Ensembl:ENSG00000129521,Ensembl:ENSG00000165389 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs566274684 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9764058,Human_RBP_ID_12318622,Human_RBP_ID_25126128 RMVar_hsa_circ_76087,RMVar_hsa_circ_165852 25631 RMVar_ID_25631 Human_SNP_ID_550736213 A-to-I Human chr14 - 34459010 34459010 34459010 AATCCCACTAGTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGGGAGGCGGAGGTTGCAGTG AATCCCACTAGTCGGGAGGCTGAGGCAGGAGATTCGCTTGAACCCGGGAGGCGGAGGTTGCAGTG T A EGLN3,SPTSSA Ensembl:ENSG00000129521,Ensembl:ENSG00000165389 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1044690895 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76087,RMVar_hsa_circ_165852 25632 RMVar_ID_25632 Human_SNP_ID_550736218 A-to-I Human chr14 - 34459033 34459033 34459033 CGAGTGTGGTGGTGGACGCCTGAAATCCCACTAGTCGGGAGGCTGAGGCAGGAGAATCGCTTGAA CGAGTGTGGTGGTGGACGCCTGAAATCCCACTGGTCGGGAGGCTGAGGCAGGAGAATCGCTTGAA T C EGLN3,SPTSSA Ensembl:ENSG00000129521,Ensembl:ENSG00000165389 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs573598890 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76087,RMVar_hsa_circ_165852 25633 RMVar_ID_25633 Human_SNP_ID_550736376 A-to-I Human chr14 - 34459493 34459493 34459493 TACAGGCATGAGCTACCACGCCTGGCCAGATTAATTTTCTTCTTTTTCTTTTTCTTTTTTTTTTT TACAGGCATGAGCTACCACGCCTGGCCAGATTGATTTTCTTCTTTTTCTTTTTCTTTTTTTTTTT T C EGLN3,SPTSSA Ensembl:ENSG00000129521,Ensembl:ENSG00000165389 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1032083071 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76087,RMVar_hsa_circ_165852 25634 RMVar_ID_25634 Human_SNP_ID_550736441 A-to-I Human chr14 - 34459705 34459705 34459705 GCCATCTTGGCTCACTGCAACCTCCGCCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCAG GCCATCTTGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCAG T C EGLN3,SPTSSA Ensembl:ENSG00000129521,Ensembl:ENSG00000165389 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1479983994 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76087,RMVar_hsa_circ_165852 25635 RMVar_ID_25635 Human_SNP_ID_550736457 A-to-I Human chr14 - 34459742 34459742 34459742 GTGTTTTGTTCTTGTTGCCCGGCTGGAGTGTAATGTCGCCATCTTGGCTCACTGCAACCTCCGCC GTGTTTTGTTCTTGTTGCCCGGCTGGAGTGTAGTGTCGCCATCTTGGCTCACTGCAACCTCCGCC T C EGLN3,SPTSSA Ensembl:ENSG00000129521,Ensembl:ENSG00000165389 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1284674616 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12318630,Human_RBP_ID_23620124 RMVar_hsa_circ_76087,RMVar_hsa_circ_165852 25636 RMVar_ID_25636 Human_SNP_ID_550754160 A-to-I Human chr14 - 34523691 34523691 34523691 AAAAATAAAAAAATAAAAAATTAGCTGAGTATAGTGATGTATGCGTGTAGACCCAGCTACTCGAT AAAAATAAAAAAATAAAAAATTAGCTGAGTATCGTGATGTATGCGTGTAGACCCAGCTACTCGAT T G EAPP Ensembl:ENSG00000129518 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1418141162 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3447303 25637 RMVar_ID_25637 Human_SNP_ID_550754257 A-to-I Human chr14 - 34524099 34524099 34524099 CTGTGAGCTACCACGCCCGGCCTTATTTTTATATTTTTAGTAGAGACAGGGTCACACCATGTTGG CTGTGAGCTACCACGCCCGGCCTTATTTTTATGTTTTTAGTAGAGACAGGGTCACACCATGTTGG T C EAPP Ensembl:ENSG00000129518 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1295730008 Functional Loss SNV dbSNP153 33..33 33 - - - 25638 RMVar_ID_25638 Human_SNP_ID_550754285 A-to-I Human chr14 - 34524198 34524198 34524198 TTTAGTACAGACAGGGTTTCACCATCTTGGCCAGGCTGATCTTGAACTCCTGACCTTGTGATCCA TTTAGTACAGACAGGGTTTCACCATCTTGGCCGGGCTGATCTTGAACTCCTGACCTTGTGATCCA T C EAPP Ensembl:ENSG00000129518 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs914398903 Functional Loss SNV dbSNP153 33..33 33 - - - 25639 RMVar_ID_25639 Human_SNP_ID_550759742 A-to-I Human chr14 + 34548849 34548849 34548849 CTTACTCACTGCAGCCTCGAACTCCTGGGTTCAAGCGGTCCTCCGGCCTCAGCCTTCCTCCTTAG CTTACTCACTGCAGCCTCGAACTCCTGGGTTCCAGCGGTCCTCCGGCCTCAGCCTTCCTCCTTAG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs528797836 Functional Loss SNV dbSNP153 33..33 33 - - - 25640 RMVar_ID_25640 Human_SNP_ID_550759743 A-to-I Human chr14 + 34548849 34548849 34548849 CTTACTCACTGCAGCCTCGAACTCCTGGGTTCAAGCGGTCCTCCGGCCTCAGCCTTCCTCCTTAG CTTACTCACTGCAGCCTCGAACTCCTGGGTTCGAGCGGTCCTCCGGCCTCAGCCTTCCTCCTTAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs528797836 Functional Loss SNV dbSNP153 33..33 33 - - - 25641 RMVar_ID_25641 Human_SNP_ID_550763810 A-to-I Human chr14 - 34566465 34566465 34566465 TCACGCCTGTAATCCCAACACTTTGGGAGGCCAAGACCGGGTGGATTATCTGAGGTCAGGTGTTC TCACGCCTGTAATCCCAACACTTTGGGAGGCCGAGACCGGGTGGATTATCTGAGGTCAGGTGTTC T C SNX6 Ensembl:ENSG00000129515 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1057360474 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91409,RMVar_hsa_circ_95775,RMVar_hsa_circ_116058,RMVar_hsa_circ_120246,RMVar_hsa_circ_104373,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_165859 25642 RMVar_ID_25642 Human_SNP_ID_550763984 A-to-I Human chr14 - 34567084 34567084 34567084 GAGTAGCTAGGACTACAGGTGCGTGCCACCACACCCAGCTAATTTTTGTATTTTTAGTAGAGACA GAGTAGCTAGGACTACAGGTGCGTGCCACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGACA T C SNX6 Ensembl:ENSG00000129515 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs977803394 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91409,RMVar_hsa_circ_95775,RMVar_hsa_circ_116058,RMVar_hsa_circ_120246,RMVar_hsa_circ_104373,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_165859 25643 RMVar_ID_25643 Human_SNP_ID_550764049 A-to-I Human chr14 - 34567252 34567252 34567252 GAAATCCCGTCCTCAAATGATCCTCCTGCCTCAGCCTCCCAAAGTGCTGAGATTACAGACACGAG GAAATCCCGTCCTCAAATGATCCTCCTGCCTCTGCCTCCCAAAGTGCTGAGATTACAGACACGAG T A SNX6 Ensembl:ENSG00000129515 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1241258267 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91409,RMVar_hsa_circ_95775,RMVar_hsa_circ_116058,RMVar_hsa_circ_120246,RMVar_hsa_circ_104373,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_165859 25644 RMVar_ID_25644 Human_SNP_ID_550764085 A-to-I Human chr14 - 34567324 34567324 34567324 TGCCACCACACCTGGGTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGTCAGGC TGCCACCACACCTGGGTAATTTTTGTATTTTTCGTAGAGACAGGGTTTCACCATGTTGGTCAGGC T G SNX6 Ensembl:ENSG00000129515 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs903758802 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91409,RMVar_hsa_circ_95775,RMVar_hsa_circ_116058,RMVar_hsa_circ_120246,RMVar_hsa_circ_104373,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_165859 25645 RMVar_ID_25645 Human_SNP_ID_550764112 A-to-I Human chr14 - 34567404 34567404 34567404 CAGTTCACTGCAACCTCTGCTTCCCGGGTTCAAGCGATTCTCACGCCTCAGCCTCCTTAGTAGCT CAGTTCACTGCAACCTCTGCTTCCCGGGTTCACGCGATTCTCACGCCTCAGCCTCCTTAGTAGCT T G SNX6 Ensembl:ENSG00000129515 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs963659000 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91409,RMVar_hsa_circ_95775,RMVar_hsa_circ_116058,RMVar_hsa_circ_120246,RMVar_hsa_circ_104373,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_165859 25646 RMVar_ID_25646 Human_SNP_ID_550764129 A-to-I Human chr14 - 34567469 34567469 34567469 TGTTTTGTTTTTTTGAGACAGAGTCTGGCGCTATTGCCCAGGCTGGAGTGCAGTGGCAATGATCT TGTTTTGTTTTTTTGAGACAGAGTCTGGCGCTGTTGCCCAGGCTGGAGTGCAGTGGCAATGATCT T C SNX6 Ensembl:ENSG00000129515 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs552776918 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91409,RMVar_hsa_circ_95775,RMVar_hsa_circ_116058,RMVar_hsa_circ_120246,RMVar_hsa_circ_104373,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_165859 25647 RMVar_ID_25647 Human_SNP_ID_550764134 A-to-I Human chr14 - 34567482 34567482 34567482 GGGTTTTTTGTTTTGTTTTGTTTTTTTGAGACAGAGTCTGGCGCTATTGCCCAGGCTGGAGTGCA GGGTTTTTTGTTTTGTTTTGTTTTTTTGAGACGGAGTCTGGCGCTATTGCCCAGGCTGGAGTGCA T C SNX6 Ensembl:ENSG00000129515 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1331470811 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91409,RMVar_hsa_circ_95775,RMVar_hsa_circ_116058,RMVar_hsa_circ_120246,RMVar_hsa_circ_104373,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_165859 25648 RMVar_ID_25648 Human_SNP_ID_550764517 A-to-I Human chr14 + 34568722 34568722 34568722 TAATGCTTCTTGTTGGCAACTGCCACCTGTCCAGCGATTCTGTCCAGATCTCTCTGTCCCTGACG TAATGCTTCTTGTTGGCAACTGCCACCTGTCCGGCGATTCTGTCCAGATCTCTCTGTCCCTGACG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879174074 Functional Loss SNV dbSNP153 33..33 33 - - - 25649 RMVar_ID_25649 Human_SNP_ID_550764557 A-to-I Human chr14 - 34568834 34568834 34568834 CATGCCTGGCCACTTTAGCCGAGGCTCCAAGAATGTGGCCCACCGGGTCCTCCAAGCCCTGGAGG CATGCCTGGCCACTTTAGCCGAGGCTCCAAGATTGTGGCCCACCGGGTCCTCCAAGCCCTGGAGG T A SNX6,RPS19P3 Ensembl:ENSG00000129515,Ensembl:ENSG00000240463 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878919435 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5095658,Human_RBP_ID_17205856 RMVar_hsa_circ_66521,RMVar_hsa_circ_91409,RMVar_hsa_circ_95775,RMVar_hsa_circ_116058,RMVar_hsa_circ_120246,RMVar_hsa_circ_104373,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_323612,RMVar_hsa_circ_165859,RMVar_hsa_circ_328016,RMVar_hsa_circ_328134,RMVar_hsa_circ_297837,RMVar_hsa_circ_80179,RMVar_hsa_circ_5330,RMVar_hsa_circ_165867,RMVar_hsa_circ_165866 25650 RMVar_ID_25650 Human_SNP_ID_550764558 A-to-I Human chr14 - 34568834 34568834 34568834 CATGCCTGGCCACTTTAGCCGAGGCTCCAAGAATGTGGCCCACCGGGTCCTCCAAGCCCTGGAGG CATGCCTGGCCACTTTAGCCGAGGCTCCAAGAGTGTGGCCCACCGGGTCCTCCAAGCCCTGGAGG T C SNX6,RPS19P3 Ensembl:ENSG00000129515,Ensembl:ENSG00000240463 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878919435 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5095658,Human_RBP_ID_17205856 RMVar_hsa_circ_66521,RMVar_hsa_circ_91409,RMVar_hsa_circ_95775,RMVar_hsa_circ_116058,RMVar_hsa_circ_120246,RMVar_hsa_circ_104373,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_323612,RMVar_hsa_circ_165859,RMVar_hsa_circ_328016,RMVar_hsa_circ_328134,RMVar_hsa_circ_297837,RMVar_hsa_circ_80179,RMVar_hsa_circ_5330,RMVar_hsa_circ_165867,RMVar_hsa_circ_165866 25651 RMVar_ID_25651 Human_SNP_ID_550765801 A-to-I Human chr14 - 34573412 34573412 34573412 TGCCACCATGCCTGGATAATTTTTGTATTTTTAGTAGATACGGGGTTTCACCATGTTGGCCAAGC TGCCACCATGCCTGGATAATTTTTGTATTTTTGGTAGATACGGGGTTTCACCATGTTGGCCAAGC T C SNX6 Ensembl:ENSG00000129515 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs749473304 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66521,RMVar_hsa_circ_91409,RMVar_hsa_circ_95775,RMVar_hsa_circ_116058,RMVar_hsa_circ_120246,RMVar_hsa_circ_104373,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_323612,RMVar_hsa_circ_165859,RMVar_hsa_circ_328016,RMVar_hsa_circ_328134,RMVar_hsa_circ_297837,RMVar_hsa_circ_80179,RMVar_hsa_circ_5330,RMVar_hsa_circ_165867,RMVar_hsa_circ_165866 25652 RMVar_ID_25652 Human_SNP_ID_550765932 A-to-I Human chr14 - 34573794 34573794 34573794 TACTAAAAATACAAAAATTAGCCAGGCATGGTAGCAGGCACCTGTAATCACAGCTACTCCAGAGG TACTAAAAATACAAAAATTAGCCAGGCATGGTGGCAGGCACCTGTAATCACAGCTACTCCAGAGG T C SNX6 Ensembl:ENSG00000129515 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs57098707 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66521,RMVar_hsa_circ_91409,RMVar_hsa_circ_95775,RMVar_hsa_circ_116058,RMVar_hsa_circ_120246,RMVar_hsa_circ_104373,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_323612,RMVar_hsa_circ_165859,RMVar_hsa_circ_328016,RMVar_hsa_circ_328134,RMVar_hsa_circ_297837,RMVar_hsa_circ_80179,RMVar_hsa_circ_5330,RMVar_hsa_circ_165867,RMVar_hsa_circ_165866 25653 RMVar_ID_25653 Human_SNP_ID_550766158 A-to-I Human chr14 - 34574550 34574550 34574550 TTCCTTCTGGGTTCAAGCGGTTTTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCTTGTG TTCCTTCTGGGTTCAAGCGGTTTTCCTGCCTCGGCCTCCTGAGTAGCTGGGATTACAGGCTTGTG T C SNX6 Ensembl:ENSG00000129515 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1257378242 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66521,RMVar_hsa_circ_91409,RMVar_hsa_circ_95775,RMVar_hsa_circ_116058,RMVar_hsa_circ_120246,RMVar_hsa_circ_104373,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_323612,RMVar_hsa_circ_165859,RMVar_hsa_circ_328016,RMVar_hsa_circ_328134,RMVar_hsa_circ_297837,RMVar_hsa_circ_80179,RMVar_hsa_circ_5330,RMVar_hsa_circ_165867,RMVar_hsa_circ_165866 25654 RMVar_ID_25654 Human_SNP_ID_550766861 A-to-I Human chr14 - 34576600 34576600 34576600 TACTAAAAATACAAAAGTTAGCCAGGCGTGGCAGTGCATGCCTGTAATTCCAGCTACTCGGGAGG TACTAAAAATACAAAAGTTAGCCAGGCGTGGCGGTGCATGCCTGTAATTCCAGCTACTCGGGAGG T C SNX6 Ensembl:ENSG00000129515 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474889349 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66521,RMVar_hsa_circ_91409,RMVar_hsa_circ_95775,RMVar_hsa_circ_116058,RMVar_hsa_circ_120246,RMVar_hsa_circ_104373,RMVar_hsa_circ_165860,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_328016,RMVar_hsa_circ_328134,RMVar_hsa_circ_297837,RMVar_hsa_circ_80179,RMVar_hsa_circ_3600,RMVar_hsa_circ_321962,RMVar_hsa_circ_5330,RMVar_hsa_circ_165866,RMVar_hsa_circ_338657,RMVar_hsa_circ_351963,RMVar_hsa_circ_323746,RMVar_hsa_circ_297373,RMVar_hsa_circ_301629,RMVar_hsa_circ_99343,RMVar_hsa_circ_165869,RMVar_hsa_circ_165871,RMVar_hsa_circ_165872,RMVar_hsa_circ_165870 25655 RMVar_ID_25655 Human_SNP_ID_550766886 A-to-I Human chr14 - 34576721 34576721 34576721 AGTCTGACTGGGCATGGTGGTTCACACCTGTAATCCCAGCACTTTGGAAGGCTGAGGCAGGAGGA AGTCTGACTGGGCATGGTGGTTCACACCTGTACTCCCAGCACTTTGGAAGGCTGAGGCAGGAGGA T G SNX6 Ensembl:ENSG00000129515 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1210787816 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66521,RMVar_hsa_circ_91409,RMVar_hsa_circ_95775,RMVar_hsa_circ_116058,RMVar_hsa_circ_120246,RMVar_hsa_circ_104373,RMVar_hsa_circ_165860,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_328016,RMVar_hsa_circ_328134,RMVar_hsa_circ_297837,RMVar_hsa_circ_80179,RMVar_hsa_circ_3600,RMVar_hsa_circ_321962,RMVar_hsa_circ_5330,RMVar_hsa_circ_165866,RMVar_hsa_circ_338657,RMVar_hsa_circ_351963,RMVar_hsa_circ_323746,RMVar_hsa_circ_297373,RMVar_hsa_circ_301629,RMVar_hsa_circ_99343,RMVar_hsa_circ_165869,RMVar_hsa_circ_165871,RMVar_hsa_circ_165872,RMVar_hsa_circ_165870 25656 RMVar_ID_25656 Human_SNP_ID_550766964 A-to-I Human chr14 - 34577016 34577016 34577016 AGACAGTCTCTCGCTCTGTCACCCAGGCTGGAATGTAGTGGCTCAATCTTGGCTCACTGCAACCT AGACAGTCTCTCGCTCTGTCACCCAGGCTGGAGTGTAGTGGCTCAATCTTGGCTCACTGCAACCT T C SNX6 Ensembl:ENSG00000129515 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs56297712 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66521,RMVar_hsa_circ_91409,RMVar_hsa_circ_95775,RMVar_hsa_circ_116058,RMVar_hsa_circ_120246,RMVar_hsa_circ_104373,RMVar_hsa_circ_165860,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_328016,RMVar_hsa_circ_328134,RMVar_hsa_circ_297837,RMVar_hsa_circ_80179,RMVar_hsa_circ_3600,RMVar_hsa_circ_321962,RMVar_hsa_circ_5330,RMVar_hsa_circ_165866,RMVar_hsa_circ_338657,RMVar_hsa_circ_351963,RMVar_hsa_circ_323746,RMVar_hsa_circ_297373,RMVar_hsa_circ_301629,RMVar_hsa_circ_99343,RMVar_hsa_circ_165869,RMVar_hsa_circ_165871,RMVar_hsa_circ_165872,RMVar_hsa_circ_165870 25657 RMVar_ID_25657 Human_SNP_ID_550767640 A-to-I Human chr14 - 34579432 34579432 34579432 GGCTAATTTTTGTAGAGAGGGAGTCTCACTACATTGCTCAGGCTGGTCTTGAACTCCTGGCCTCT GGCTAATTTTTGTAGAGAGGGAGTCTCACTACGTTGCTCAGGCTGGTCTTGAACTCCTGGCCTCT T C SNX6 Ensembl:ENSG00000129515 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs555065102 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66521,RMVar_hsa_circ_91409,RMVar_hsa_circ_95775,RMVar_hsa_circ_116058,RMVar_hsa_circ_120246,RMVar_hsa_circ_104373,RMVar_hsa_circ_165860,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_328016,RMVar_hsa_circ_328134,RMVar_hsa_circ_297837,RMVar_hsa_circ_80179,RMVar_hsa_circ_3600,RMVar_hsa_circ_321962,RMVar_hsa_circ_5330,RMVar_hsa_circ_165866,RMVar_hsa_circ_338657,RMVar_hsa_circ_351963,RMVar_hsa_circ_323746,RMVar_hsa_circ_297373,RMVar_hsa_circ_301629,RMVar_hsa_circ_99343,RMVar_hsa_circ_165869,RMVar_hsa_circ_165871,RMVar_hsa_circ_165872,RMVar_hsa_circ_165870 25658 RMVar_ID_25658 Human_SNP_ID_550767655 A-to-I Human chr14 - 34579492 34579492 34579492 AGCATCCTCTTGCCTCAGCCTCCCAAGTAGTTAGGACTACAGATGTGTGTTACCATGCCTGGCTA AGCATCCTCTTGCCTCAGCCTCCCAAGTAGTTTGGACTACAGATGTGTGTTACCATGCCTGGCTA T A SNX6 Ensembl:ENSG00000129515 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1482034856 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66521,RMVar_hsa_circ_91409,RMVar_hsa_circ_95775,RMVar_hsa_circ_116058,RMVar_hsa_circ_120246,RMVar_hsa_circ_104373,RMVar_hsa_circ_165860,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_328016,RMVar_hsa_circ_328134,RMVar_hsa_circ_297837,RMVar_hsa_circ_80179,RMVar_hsa_circ_3600,RMVar_hsa_circ_321962,RMVar_hsa_circ_5330,RMVar_hsa_circ_165866,RMVar_hsa_circ_338657,RMVar_hsa_circ_351963,RMVar_hsa_circ_323746,RMVar_hsa_circ_297373,RMVar_hsa_circ_301629,RMVar_hsa_circ_99343,RMVar_hsa_circ_165869,RMVar_hsa_circ_165871,RMVar_hsa_circ_165872,RMVar_hsa_circ_165870 25659 RMVar_ID_25659 Human_SNP_ID_550767896 A-to-I Human chr14 - 34580440 34580440 34580440 AAAATTAGCCAGGCGTGGTGGCGCACAACTGTAGTCCTAACTACTTGGGAGGCTGAGGCAGGAAG AAAATTAGCCAGGCGTGGTGGCGCACAACTGTTGTCCTAACTACTTGGGAGGCTGAGGCAGGAAG T A SNX6 Ensembl:ENSG00000129515 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1404110685 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66521,RMVar_hsa_circ_91409,RMVar_hsa_circ_95775,RMVar_hsa_circ_116058,RMVar_hsa_circ_120246,RMVar_hsa_circ_104373,RMVar_hsa_circ_165860,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_328016,RMVar_hsa_circ_328134,RMVar_hsa_circ_297837,RMVar_hsa_circ_80179,RMVar_hsa_circ_3600,RMVar_hsa_circ_321962,RMVar_hsa_circ_5330,RMVar_hsa_circ_165866,RMVar_hsa_circ_338657,RMVar_hsa_circ_351963,RMVar_hsa_circ_323746,RMVar_hsa_circ_297373,RMVar_hsa_circ_301629,RMVar_hsa_circ_99343,RMVar_hsa_circ_165869,RMVar_hsa_circ_165871,RMVar_hsa_circ_165872,RMVar_hsa_circ_165870 25660 RMVar_ID_25660 Human_SNP_ID_550767897 A-to-I Human chr14 - 34580440 34580440 34580440 AAAATTAGCCAGGCGTGGTGGCGCACAACTGTAGTCCTAACTACTTGGGAGGCTGAGGCAGGAAG AAAATTAGCCAGGCGTGGTGGCGCACAACTGTCGTCCTAACTACTTGGGAGGCTGAGGCAGGAAG T G SNX6 Ensembl:ENSG00000129515 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1404110685 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66521,RMVar_hsa_circ_91409,RMVar_hsa_circ_95775,RMVar_hsa_circ_116058,RMVar_hsa_circ_120246,RMVar_hsa_circ_104373,RMVar_hsa_circ_165860,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_328016,RMVar_hsa_circ_328134,RMVar_hsa_circ_297837,RMVar_hsa_circ_80179,RMVar_hsa_circ_3600,RMVar_hsa_circ_321962,RMVar_hsa_circ_5330,RMVar_hsa_circ_165866,RMVar_hsa_circ_338657,RMVar_hsa_circ_351963,RMVar_hsa_circ_323746,RMVar_hsa_circ_297373,RMVar_hsa_circ_301629,RMVar_hsa_circ_99343,RMVar_hsa_circ_165869,RMVar_hsa_circ_165871,RMVar_hsa_circ_165872,RMVar_hsa_circ_165870 25661 RMVar_ID_25661 Human_SNP_ID_550768089 A-to-I Human chr14 - 34581222 34581222 34581222 TTGAACCCGGGAGGCCAACGTTGTAGTGAGCCAAGATTGCACCACTGCACTCCAGCCTGGCGAGA TTGAACCCGGGAGGCCAACGTTGTAGTGAGCCGAGATTGCACCACTGCACTCCAGCCTGGCGAGA T C SNX6 Ensembl:ENSG00000129515 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs777126423 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66521,RMVar_hsa_circ_91409,RMVar_hsa_circ_95775,RMVar_hsa_circ_116058,RMVar_hsa_circ_120246,RMVar_hsa_circ_104373,RMVar_hsa_circ_165860,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_328016,RMVar_hsa_circ_328134,RMVar_hsa_circ_297837,RMVar_hsa_circ_80179,RMVar_hsa_circ_3600,RMVar_hsa_circ_321962,RMVar_hsa_circ_5330,RMVar_hsa_circ_165866,RMVar_hsa_circ_338657,RMVar_hsa_circ_351963,RMVar_hsa_circ_323746,RMVar_hsa_circ_297373,RMVar_hsa_circ_301629,RMVar_hsa_circ_99343,RMVar_hsa_circ_165869,RMVar_hsa_circ_165871,RMVar_hsa_circ_165872,RMVar_hsa_circ_165870 25662 RMVar_ID_25662 Human_SNP_ID_550768104 A-to-I Human chr14 - 34581294 34581294 34581294 CAAAAATTAGTTGGGCGTGGTGACGCATGCCTATAGTCCCAGCTACTTGGGAGGCTGAGGCACAA CAAAAATTAGTTGGGCGTGGTGACGCATGCCTTTAGTCCCAGCTACTTGGGAGGCTGAGGCACAA T A SNX6 Ensembl:ENSG00000129515 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs896792443 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66521,RMVar_hsa_circ_91409,RMVar_hsa_circ_95775,RMVar_hsa_circ_116058,RMVar_hsa_circ_120246,RMVar_hsa_circ_104373,RMVar_hsa_circ_165860,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_328016,RMVar_hsa_circ_328134,RMVar_hsa_circ_297837,RMVar_hsa_circ_80179,RMVar_hsa_circ_3600,RMVar_hsa_circ_321962,RMVar_hsa_circ_5330,RMVar_hsa_circ_165866,RMVar_hsa_circ_338657,RMVar_hsa_circ_351963,RMVar_hsa_circ_323746,RMVar_hsa_circ_297373,RMVar_hsa_circ_301629,RMVar_hsa_circ_99343,RMVar_hsa_circ_165869,RMVar_hsa_circ_165871,RMVar_hsa_circ_165872,RMVar_hsa_circ_165870 25663 RMVar_ID_25663 Human_SNP_ID_550768105 A-to-I Human chr14 - 34581294 34581294 34581294 CAAAAATTAGTTGGGCGTGGTGACGCATGCCTATAGTCCCAGCTACTTGGGAGGCTGAGGCACAA CAAAAATTAGTTGGGCGTGGTGACGCATGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCACAA T C SNX6 Ensembl:ENSG00000129515 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs896792443 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66521,RMVar_hsa_circ_91409,RMVar_hsa_circ_95775,RMVar_hsa_circ_116058,RMVar_hsa_circ_120246,RMVar_hsa_circ_104373,RMVar_hsa_circ_165860,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_328016,RMVar_hsa_circ_328134,RMVar_hsa_circ_297837,RMVar_hsa_circ_80179,RMVar_hsa_circ_3600,RMVar_hsa_circ_321962,RMVar_hsa_circ_5330,RMVar_hsa_circ_165866,RMVar_hsa_circ_338657,RMVar_hsa_circ_351963,RMVar_hsa_circ_323746,RMVar_hsa_circ_297373,RMVar_hsa_circ_301629,RMVar_hsa_circ_99343,RMVar_hsa_circ_165869,RMVar_hsa_circ_165871,RMVar_hsa_circ_165872,RMVar_hsa_circ_165870 25664 RMVar_ID_25664 Human_SNP_ID_550768299 A-to-I Human chr14 - 34581914 34581914 34581914 TGAGGCTGGAGAATCGCTTGAACTCGGGAGGCAGAGGTTACAGTGAGCTGAGATTGCGCAGTTGC TGAGGCTGGAGAATCGCTTGAACTCGGGAGGCTGAGGTTACAGTGAGCTGAGATTGCGCAGTTGC T A SNX6 Ensembl:ENSG00000129515 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4258505 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2443,GWAS_ID_2444 RMVar_hsa_circ_66521,RMVar_hsa_circ_91409,RMVar_hsa_circ_95775,RMVar_hsa_circ_116058,RMVar_hsa_circ_120246,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_328016,RMVar_hsa_circ_328134,RMVar_hsa_circ_80179,RMVar_hsa_circ_23383,RMVar_hsa_circ_3600,RMVar_hsa_circ_321962,RMVar_hsa_circ_5330,RMVar_hsa_circ_165866,RMVar_hsa_circ_338657,RMVar_hsa_circ_351963,RMVar_hsa_circ_323746,RMVar_hsa_circ_297373,RMVar_hsa_circ_301629,RMVar_hsa_circ_99343,RMVar_hsa_circ_165869,RMVar_hsa_circ_165871,RMVar_hsa_circ_165872,RMVar_hsa_circ_165870,RMVar_hsa_circ_345051,RMVar_hsa_circ_378348,RMVar_hsa_circ_72881,RMVar_hsa_circ_165873 25665 RMVar_ID_25665 Human_SNP_ID_550768300 A-to-I Human chr14 - 34581914 34581914 34581914 TGAGGCTGGAGAATCGCTTGAACTCGGGAGGCAGAGGTTACAGTGAGCTGAGATTGCGCAGTTGC TGAGGCTGGAGAATCGCTTGAACTCGGGAGGCGGAGGTTACAGTGAGCTGAGATTGCGCAGTTGC T C SNX6 Ensembl:ENSG00000129515 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4258505 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2443,GWAS_ID_2444 RMVar_hsa_circ_66521,RMVar_hsa_circ_91409,RMVar_hsa_circ_95775,RMVar_hsa_circ_116058,RMVar_hsa_circ_120246,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_328016,RMVar_hsa_circ_328134,RMVar_hsa_circ_80179,RMVar_hsa_circ_23383,RMVar_hsa_circ_3600,RMVar_hsa_circ_321962,RMVar_hsa_circ_5330,RMVar_hsa_circ_165866,RMVar_hsa_circ_338657,RMVar_hsa_circ_351963,RMVar_hsa_circ_323746,RMVar_hsa_circ_297373,RMVar_hsa_circ_301629,RMVar_hsa_circ_99343,RMVar_hsa_circ_165869,RMVar_hsa_circ_165871,RMVar_hsa_circ_165872,RMVar_hsa_circ_165870,RMVar_hsa_circ_345051,RMVar_hsa_circ_378348,RMVar_hsa_circ_72881,RMVar_hsa_circ_165873 25666 RMVar_ID_25666 Human_SNP_ID_550768930 A-to-I Human chr14 - 34584126 34584126 34584126 TAAAATGCCACCAGCCGGGCACAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGC TAAAATGCCACCAGCCGGGCACAGTGGCTCACTCCTGTAATCCCAGCACTTTGGGAGGCCAAGGC T A SNX6 Ensembl:ENSG00000129515 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1214571132 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66521,RMVar_hsa_circ_91409,RMVar_hsa_circ_95775,RMVar_hsa_circ_116058,RMVar_hsa_circ_120246,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_328016,RMVar_hsa_circ_328134,RMVar_hsa_circ_80179,RMVar_hsa_circ_23383,RMVar_hsa_circ_3600,RMVar_hsa_circ_321962,RMVar_hsa_circ_5330,RMVar_hsa_circ_165866,RMVar_hsa_circ_338657,RMVar_hsa_circ_351963,RMVar_hsa_circ_323746,RMVar_hsa_circ_297373,RMVar_hsa_circ_301629,RMVar_hsa_circ_99343,RMVar_hsa_circ_165869,RMVar_hsa_circ_165871,RMVar_hsa_circ_165872,RMVar_hsa_circ_165870,RMVar_hsa_circ_345051,RMVar_hsa_circ_378348,RMVar_hsa_circ_72881,RMVar_hsa_circ_165873 25667 RMVar_ID_25667 Human_SNP_ID_550769264 A-to-I Human chr14 - 34585357 34585357 34585357 TGCCACCATGCCTGGCTAATTCTTGTATTTTTAGTAGAGATGGGGTTTCACCATATTGGCCAGGC TGCCACCATGCCTGGCTAATTCTTGTATTTTTGGTAGAGATGGGGTTTCACCATATTGGCCAGGC T C SNX6 Ensembl:ENSG00000129515 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1217271553 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66521,RMVar_hsa_circ_91409,RMVar_hsa_circ_95775,RMVar_hsa_circ_116058,RMVar_hsa_circ_120246,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_328016,RMVar_hsa_circ_328134,RMVar_hsa_circ_80179,RMVar_hsa_circ_23383,RMVar_hsa_circ_3600,RMVar_hsa_circ_321962,RMVar_hsa_circ_5330,RMVar_hsa_circ_165866,RMVar_hsa_circ_338657,RMVar_hsa_circ_351963,RMVar_hsa_circ_323746,RMVar_hsa_circ_297373,RMVar_hsa_circ_301629,RMVar_hsa_circ_99343,RMVar_hsa_circ_165869,RMVar_hsa_circ_165871,RMVar_hsa_circ_165872,RMVar_hsa_circ_165870,RMVar_hsa_circ_345051,RMVar_hsa_circ_378348,RMVar_hsa_circ_72881,RMVar_hsa_circ_165873 25668 RMVar_ID_25668 Human_SNP_ID_550771975 A-to-I Human chr14 - 34595275 34595275 34595275 AAATTAGCCAGGCATGGTGGCACGTGGCTGTAATCCCAGCTACTCGGGAGGCTTTTGAGGCAGGA AAATTAGCCAGGCATGGTGGCACGTGGCTGTAGTCCCAGCTACTCGGGAGGCTTTTGAGGCAGGA T C SNX6 Ensembl:ENSG00000129515 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs952091196 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91409,RMVar_hsa_circ_95775,RMVar_hsa_circ_116058,RMVar_hsa_circ_120246,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_328134,RMVar_hsa_circ_80179,RMVar_hsa_circ_23383,RMVar_hsa_circ_3600,RMVar_hsa_circ_321962,RMVar_hsa_circ_5330,RMVar_hsa_circ_165866,RMVar_hsa_circ_338657,RMVar_hsa_circ_351963,RMVar_hsa_circ_297373,RMVar_hsa_circ_99343,RMVar_hsa_circ_165871,RMVar_hsa_circ_165872,RMVar_hsa_circ_345051,RMVar_hsa_circ_72881,RMVar_hsa_circ_299138,RMVar_hsa_circ_165873,RMVar_hsa_circ_368849,RMVar_hsa_circ_318290,RMVar_hsa_circ_165875,RMVar_hsa_circ_276138,RMVar_hsa_circ_165874,RMVar_hsa_circ_290770,RMVar_hsa_circ_61415,RMVar_hsa_circ_165876 25669 RMVar_ID_25669 Human_SNP_ID_550772854 A-to-I Human chr14 - 34598800 34598800 34598800 AGCACATTGCAGCCTCAAACTCCTGGCGTCAAATGATCCTCCCACCTCAGCCTCCCAAGTAGCTG AGCACATTGCAGCCTCAAACTCCTGGCGTCAATTGATCCTCCCACCTCAGCCTCCCAAGTAGCTG T A SNX6 Ensembl:ENSG00000129515 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1489438498 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91409,RMVar_hsa_circ_95775,RMVar_hsa_circ_116058,RMVar_hsa_circ_120246,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_328134,RMVar_hsa_circ_80179,RMVar_hsa_circ_13050,RMVar_hsa_circ_3600,RMVar_hsa_circ_321962,RMVar_hsa_circ_5330,RMVar_hsa_circ_165866,RMVar_hsa_circ_351963,RMVar_hsa_circ_297373,RMVar_hsa_circ_99343,RMVar_hsa_circ_165871,RMVar_hsa_circ_165872,RMVar_hsa_circ_345051,RMVar_hsa_circ_72881,RMVar_hsa_circ_165873,RMVar_hsa_circ_368849,RMVar_hsa_circ_318290,RMVar_hsa_circ_165875,RMVar_hsa_circ_276138,RMVar_hsa_circ_165874,RMVar_hsa_circ_290770,RMVar_hsa_circ_61415,RMVar_hsa_circ_165876,RMVar_hsa_circ_300499,RMVar_hsa_circ_165878 25670 RMVar_ID_25670 Human_SNP_ID_550772855 A-to-I Human chr14 - 34598800 34598800 34598800 AGCACATTGCAGCCTCAAACTCCTGGCGTCAAATGATCCTCCCACCTCAGCCTCCCAAGTAGCTG AGCACATTGCAGCCTCAAACTCCTGGCGTCAAGTGATCCTCCCACCTCAGCCTCCCAAGTAGCTG T C SNX6 Ensembl:ENSG00000129515 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1489438498 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91409,RMVar_hsa_circ_95775,RMVar_hsa_circ_116058,RMVar_hsa_circ_120246,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_328134,RMVar_hsa_circ_80179,RMVar_hsa_circ_13050,RMVar_hsa_circ_3600,RMVar_hsa_circ_321962,RMVar_hsa_circ_5330,RMVar_hsa_circ_165866,RMVar_hsa_circ_351963,RMVar_hsa_circ_297373,RMVar_hsa_circ_99343,RMVar_hsa_circ_165871,RMVar_hsa_circ_165872,RMVar_hsa_circ_345051,RMVar_hsa_circ_72881,RMVar_hsa_circ_165873,RMVar_hsa_circ_368849,RMVar_hsa_circ_318290,RMVar_hsa_circ_165875,RMVar_hsa_circ_276138,RMVar_hsa_circ_165874,RMVar_hsa_circ_290770,RMVar_hsa_circ_61415,RMVar_hsa_circ_165876,RMVar_hsa_circ_300499,RMVar_hsa_circ_165878 25671 RMVar_ID_25671 Human_SNP_ID_550773215 A-to-I Human chr14 - 34600253 34600253 34600253 GGACGTGGTGGCGCTTGCCTGTAATCCCAGCTACTTGGGAGGCTGAGACATGAGAATCACTTGAA GGACGTGGTGGCGCTTGCCTGTAATCCCAGCTTCTTGGGAGGCTGAGACATGAGAATCACTTGAA T A SNX6 Ensembl:ENSG00000129515 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017185936 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91409,RMVar_hsa_circ_95775,RMVar_hsa_circ_116058,RMVar_hsa_circ_120246,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_328134,RMVar_hsa_circ_80179,RMVar_hsa_circ_13050,RMVar_hsa_circ_3600,RMVar_hsa_circ_321962,RMVar_hsa_circ_5330,RMVar_hsa_circ_165866,RMVar_hsa_circ_351963,RMVar_hsa_circ_297373,RMVar_hsa_circ_99343,RMVar_hsa_circ_165871,RMVar_hsa_circ_165872,RMVar_hsa_circ_345051,RMVar_hsa_circ_72881,RMVar_hsa_circ_165873,RMVar_hsa_circ_368849,RMVar_hsa_circ_318290,RMVar_hsa_circ_165875,RMVar_hsa_circ_276138,RMVar_hsa_circ_165874,RMVar_hsa_circ_290770,RMVar_hsa_circ_61415,RMVar_hsa_circ_165876,RMVar_hsa_circ_300499,RMVar_hsa_circ_165878 25672 RMVar_ID_25672 Human_SNP_ID_550773818 A-to-I Human chr14 - 34602191 34602191 34602191 AAACTCCCAGCCTCAGGTGATCCTCCCACCTTAGCCTCCCAAAGTGCTGGGATTACATGCATGAG AAACTCCCAGCCTCAGGTGATCCTCCCACCTTGGCCTCCCAAAGTGCTGGGATTACATGCATGAG T C SNX6 Ensembl:ENSG00000129515 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1009262679 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91409,RMVar_hsa_circ_95775,RMVar_hsa_circ_116058,RMVar_hsa_circ_120246,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_328134,RMVar_hsa_circ_80179,RMVar_hsa_circ_13050,RMVar_hsa_circ_3600,RMVar_hsa_circ_321962,RMVar_hsa_circ_5330,RMVar_hsa_circ_165866,RMVar_hsa_circ_351963,RMVar_hsa_circ_297373,RMVar_hsa_circ_99343,RMVar_hsa_circ_165871,RMVar_hsa_circ_165872,RMVar_hsa_circ_345051,RMVar_hsa_circ_72881,RMVar_hsa_circ_165873,RMVar_hsa_circ_368849,RMVar_hsa_circ_318290,RMVar_hsa_circ_165875,RMVar_hsa_circ_276138,RMVar_hsa_circ_165874,RMVar_hsa_circ_290770,RMVar_hsa_circ_61415,RMVar_hsa_circ_165876,RMVar_hsa_circ_300499,RMVar_hsa_circ_165878 25673 RMVar_ID_25673 Human_SNP_ID_550773856 A-to-I Human chr14 - 34602340 34602340 34602340 TCACCCACAACCTCTGCCTCCTTGGTTCAAGCAATTCTTCTGCCTCAGACTCTCAAGTAGCTGGG TCACCCACAACCTCTGCCTCCTTGGTTCAAGCCATTCTTCTGCCTCAGACTCTCAAGTAGCTGGG T G SNX6 Ensembl:ENSG00000129515 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1291946419 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91409,RMVar_hsa_circ_95775,RMVar_hsa_circ_116058,RMVar_hsa_circ_120246,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_328134,RMVar_hsa_circ_80179,RMVar_hsa_circ_13050,RMVar_hsa_circ_3600,RMVar_hsa_circ_321962,RMVar_hsa_circ_5330,RMVar_hsa_circ_165866,RMVar_hsa_circ_351963,RMVar_hsa_circ_297373,RMVar_hsa_circ_99343,RMVar_hsa_circ_165871,RMVar_hsa_circ_165872,RMVar_hsa_circ_345051,RMVar_hsa_circ_72881,RMVar_hsa_circ_165873,RMVar_hsa_circ_368849,RMVar_hsa_circ_318290,RMVar_hsa_circ_165875,RMVar_hsa_circ_276138,RMVar_hsa_circ_165874,RMVar_hsa_circ_290770,RMVar_hsa_circ_61415,RMVar_hsa_circ_165876,RMVar_hsa_circ_300499,RMVar_hsa_circ_165878 25674 RMVar_ID_25674 Human_SNP_ID_550775273 A-to-I Human chr14 - 34607064 34607064 34607064 GTTTTAAAACCATGGTTGGGGCTGGGCACGGTAGCTCATGCCTGTAATCCCAGCACTTTGGGAGG GTTTTAAAACCATGGTTGGGGCTGGGCACGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGG T C SNX6 Ensembl:ENSG00000129515 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1328561113 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91409,RMVar_hsa_circ_116058,RMVar_hsa_circ_86040,RMVar_hsa_circ_165864,RMVar_hsa_circ_165865,RMVar_hsa_circ_165863,RMVar_hsa_circ_328134,RMVar_hsa_circ_13050,RMVar_hsa_circ_3600,RMVar_hsa_circ_5330,RMVar_hsa_circ_351963,RMVar_hsa_circ_297373,RMVar_hsa_circ_165872,RMVar_hsa_circ_345051,RMVar_hsa_circ_165873,RMVar_hsa_circ_368849,RMVar_hsa_circ_165875,RMVar_hsa_circ_276138,RMVar_hsa_circ_290770,RMVar_hsa_circ_61415,RMVar_hsa_circ_165876,RMVar_hsa_circ_300499,RMVar_hsa_circ_3496,RMVar_hsa_circ_321478,RMVar_hsa_circ_165878,RMVar_hsa_circ_316933,RMVar_hsa_circ_320844,RMVar_hsa_circ_165879 25675 RMVar_ID_25675 Human_SNP_ID_550776464 A-to-I Human chr14 - 34611311 34611311 34611311 ACATGTGCCCGGCTAATTTTTGTATTTTTTGTAGAGATGGGGTTTTGCCGTGTTGGCCAGGCTAG ACATGTGCCCGGCTAATTTTTGTATTTTTTGTGGAGATGGGGTTTTGCCGTGTTGGCCAGGCTAG T C SNX6 Ensembl:ENSG00000129515 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs573656524 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91409,RMVar_hsa_circ_116058,RMVar_hsa_circ_165864,RMVar_hsa_circ_165865,RMVar_hsa_circ_3600,RMVar_hsa_circ_3496 25676 RMVar_ID_25676 Human_SNP_ID_550776480 A-to-I Human chr14 - 34611376 34611376 34611376 ACCTCTTGGGCTCAAGCCATTCCCCACACCTCAGCCTCCCAAGTAGCTGGGACTACAGGTGTACA ACCTCTTGGGCTCAAGCCATTCCCCACACCTCCGCCTCCCAAGTAGCTGGGACTACAGGTGTACA T G SNX6 Ensembl:ENSG00000129515 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1490667240 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17562440 RMVar_hsa_circ_91409,RMVar_hsa_circ_116058,RMVar_hsa_circ_165864,RMVar_hsa_circ_165865,RMVar_hsa_circ_3600,RMVar_hsa_circ_3496 25677 RMVar_ID_25677 Human_SNP_ID_550776864 A-to-I Human chr14 - 34612562 34612562 34612562 GGGCCTGGTTGTGCATGCCTGTAGTCCTAGCTACTCGGGAGGTTGAGGCAGGAGAATCACTTGAA GGGCCTGGTTGTGCATGCCTGTAGTCCTAGCTGCTCGGGAGGTTGAGGCAGGAGAATCACTTGAA T C SNX6 Ensembl:ENSG00000129515 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs532689728 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91409,RMVar_hsa_circ_116058,RMVar_hsa_circ_165864,RMVar_hsa_circ_165865,RMVar_hsa_circ_3600,RMVar_hsa_circ_3496 25678 RMVar_ID_25678 Human_SNP_ID_550776896 A-to-I Human chr14 - 34612709 34612709 34612709 AATGTCCTGGCTCGGCGTGGTGGCTCACGCCTATAATCCCAACACTTTGGGAGGCTGAGGCAGGT AATGTCCTGGCTCGGCGTGGTGGCTCACGCCTGTAATCCCAACACTTTGGGAGGCTGAGGCAGGT T C SNX6 Ensembl:ENSG00000129515 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264004544 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91409,RMVar_hsa_circ_116058,RMVar_hsa_circ_165864,RMVar_hsa_circ_165865,RMVar_hsa_circ_3600,RMVar_hsa_circ_3496 25679 RMVar_ID_25679 Human_SNP_ID_550777913 A-to-I Human chr14 - 34616508 34616508 34616508 AAAATTAGCTGGGCATGGTGATGTGTGCCTGTAGTCCCAGCTACCTGGAAGGCTGAGATGGAATG AAAATTAGCTGGGCATGGTGATGTGTGCCTGTGGTCCCAGCTACCTGGAAGGCTGAGATGGAATG T C SNX6 Ensembl:ENSG00000129515 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1011342727 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17562441 RMVar_hsa_circ_91409,RMVar_hsa_circ_116058,RMVar_hsa_circ_165864,RMVar_hsa_circ_165865,RMVar_hsa_circ_3600,RMVar_hsa_circ_3496 25680 RMVar_ID_25680 Human_SNP_ID_550779109 A-to-I Human chr14 - 34620928 34620928 34620928 TTTATTTTTTATTTTTTTTTTGAGGGAGTCTCACTTTATCACCCAGGTTGGAGTGCAGTGGCACC TTTATTTTTTATTTTTTTTTTGAGGGAGTCTCGCTTTATCACCCAGGTTGGAGTGCAGTGGCACC T C SNX6 Ensembl:ENSG00000129515 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1239501826 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12460306 RMVar_hsa_circ_91409,RMVar_hsa_circ_116058,RMVar_hsa_circ_165864,RMVar_hsa_circ_165865,RMVar_hsa_circ_3600,RMVar_hsa_circ_3496 25681 RMVar_ID_25681 Human_SNP_ID_550779193 A-to-I Human chr14 - 34621222 34621222 34621222 GTTGAGAGAAGCTGACGCAGTGGCTCATGTCTATAATCCTAGCACTCTGAGAGGCTGAGGCAAGA GTTGAGAGAAGCTGACGCAGTGGCTCATGTCTGTAATCCTAGCACTCTGAGAGGCTGAGGCAAGA T C SNX6 Ensembl:ENSG00000129515 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs755539091 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22711668 RMVar_hsa_circ_91409,RMVar_hsa_circ_116058,RMVar_hsa_circ_165864,RMVar_hsa_circ_165865,RMVar_hsa_circ_3600,RMVar_hsa_circ_3496 25682 RMVar_ID_25682 Human_SNP_ID_550780107 A-to-I Human chr14 - 34624563 34624563 34624563 TTGATCTCTTGACTTCATGATCCACCCTCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG TTGATCTCTTGACTTCATGATCCACCCTCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG T C SNX6 Ensembl:ENSG00000129515 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs71419999 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91409,RMVar_hsa_circ_116058,RMVar_hsa_circ_165864,RMVar_hsa_circ_165865,RMVar_hsa_circ_3600,RMVar_hsa_circ_3496 25683 RMVar_ID_25683 Human_SNP_ID_550780812 A-to-I Human chr14 - 34627118 34627118 34627118 AAACTTAGGCAAGCTTGGTGGTATATACCTGTAGTCCTAGCTATTTGAGAGGCTGAGAGCTTGAG AAACTTAGGCAAGCTTGGTGGTATATACCTGTGGTCCTAGCTATTTGAGAGGCTGAGAGCTTGAG T C SNX6 Ensembl:ENSG00000129515 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1431056709 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12319498,Human_RBP_ID_23160842 RMVar_hsa_circ_91409,RMVar_hsa_circ_116058,RMVar_hsa_circ_165864,RMVar_hsa_circ_165865,RMVar_hsa_circ_3600,RMVar_hsa_circ_3496 25684 RMVar_ID_25684 Human_SNP_ID_550780814 A-to-I Human chr14 - 34627124 34627123 34627125 TTTTTTAAACTTAGGCAAGCTTGGTGGTATATACCTGTAGTCCTAGCTATTTGAGAGGCTGAGAG TTTTTTAAACTTAGGCAAGCTTGGTGGTATA__CCTGTAGTCCTAGCTATTTGAGAGGCTGAGAG GTA G SNX6 Ensembl:ENSG00000129515 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1271943309 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_12319498,Human_RBP_ID_23160842 RMVar_hsa_circ_91409,RMVar_hsa_circ_116058,RMVar_hsa_circ_165864,RMVar_hsa_circ_165865,RMVar_hsa_circ_3600,RMVar_hsa_circ_3496 25685 RMVar_ID_25685 Human_SNP_ID_550803277 A-to-I Human chr14 - 34712722 34712720 34712723 GCCCTTCCAACACAATGAATGAAGGAAATATCATTTATTTAAGCAGCCTATCAGTGATTGCCATT GCCCTTCCAACACAATGAATGAAGGAAATAT___TTATTTAAGCAGCCTATCAGTGATTGCCATT AATG A CFL2 Ensembl:ENSG00000165410 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1266728826 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_445037,Human_RBP_ID_1818281,Human_RBP_ID_6342529,Human_RBP_ID_8181703,Human_RBP_ID_9041230,Human_RBP_ID_17247091,Human_RBP_ID_17478918,Human_RBP_ID_18273040,Human_RBP_ID_24410876,Human_RBP_ID_24471332,Human_RBP_ID_27644257 25686 RMVar_ID_25686 Human_SNP_ID_550815704 A-to-I Human chr14 - 34758377 34758377 34758377 CGGGGTTTCAACATGTTGGTCAGGCTGGTCTCAATCTCCTGACCTTGTGATCTGCCCACCTCGGC CGGGGTTTCAACATGTTGGTCAGGCTGGTCTCGATCTCCTGACCTTGTGATCTGCCCACCTCGGC T C BAZ1A Ensembl:ENSG00000198604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs185609117 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88530,RMVar_hsa_circ_165884,RMVar_hsa_circ_366915,RMVar_hsa_circ_165883,RMVar_hsa_circ_317181 25687 RMVar_ID_25687 Human_SNP_ID_550815705 A-to-I Human chr14 - 34758377 34758377 34758377 CGGGGTTTCAACATGTTGGTCAGGCTGGTCTCAATCTCCTGACCTTGTGATCTGCCCACCTCGGC CGGGGTTTCAACATGTTGGTCAGGCTGGTCTCCATCTCCTGACCTTGTGATCTGCCCACCTCGGC T G BAZ1A Ensembl:ENSG00000198604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs185609117 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88530,RMVar_hsa_circ_165884,RMVar_hsa_circ_366915,RMVar_hsa_circ_165883,RMVar_hsa_circ_317181 25688 RMVar_ID_25688 Human_SNP_ID_550822848 A-to-I Human chr14 - 34787422 34787422 34787422 CCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCGCCCGGCCCCCACTGGTTTTT CCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCCCGGCCCCCACTGGTTTTT T C BAZ1A Ensembl:ENSG00000198604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1041792234 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25094920 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_372304,RMVar_hsa_circ_87745,RMVar_hsa_circ_111427,RMVar_hsa_circ_165891,RMVar_hsa_circ_65146,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_296823,RMVar_hsa_circ_165895,RMVar_hsa_circ_165896,RMVar_hsa_circ_365963,RMVar_hsa_circ_165898,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_273898,RMVar_hsa_circ_52749,RMVar_hsa_circ_111170,RMVar_hsa_circ_165903,RMVar_hsa_circ_165904,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_165905 25689 RMVar_ID_25689 Human_SNP_ID_550823021 A-to-I Human chr14 - 34788117 34788117 34788117 GCTACCTGGGAGGCTGAGGCAGAGAATTGCTTAAACCTGGGAGGCGGAGGTTGCAGTGAGCCAAG GCTACCTGGGAGGCTGAGGCAGAGAATTGCTTGAACCTGGGAGGCGGAGGTTGCAGTGAGCCAAG T C BAZ1A Ensembl:ENSG00000198604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1481273845 Functional Loss SNV dbSNP153 33..33 33 - - - 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_372304,RMVar_hsa_circ_87745,RMVar_hsa_circ_111427,RMVar_hsa_circ_165891,RMVar_hsa_circ_65146,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_296823,RMVar_hsa_circ_165895,RMVar_hsa_circ_165896,RMVar_hsa_circ_365963,RMVar_hsa_circ_165898,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_273898,RMVar_hsa_circ_52749,RMVar_hsa_circ_111170,RMVar_hsa_circ_165903,RMVar_hsa_circ_165904,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_165905 25690 RMVar_ID_25690 Human_SNP_ID_550823115 A-to-I Human chr14 - 34788442 34788442 34788442 AAAACTAGGTGGGCATGGTGGCATGCGCCTGTAGTCCCAGCTACTGGGGAGGCCGAGGTGGGAGG AAAACTAGGTGGGCATGGTGGCATGCGCCTGTTGTCCCAGCTACTGGGGAGGCCGAGGTGGGAGG T A BAZ1A Ensembl:ENSG00000198604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1405499607 Functional Loss SNV dbSNP153 33..33 33 - - - 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_372304,RMVar_hsa_circ_87745,RMVar_hsa_circ_111427,RMVar_hsa_circ_165891,RMVar_hsa_circ_65146,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_296823,RMVar_hsa_circ_165895,RMVar_hsa_circ_165896,RMVar_hsa_circ_365963,RMVar_hsa_circ_165898,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_273898,RMVar_hsa_circ_52749,RMVar_hsa_circ_111170,RMVar_hsa_circ_165903,RMVar_hsa_circ_165904,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_165905 25691 RMVar_ID_25691 Human_SNP_ID_550823545 A-to-I Human chr14 - 34790620 34790620 34790620 GCTGGGTGTGGTGGCTCATGCCTGTAATCCCAACATTTTGGGAGGCTGAGGTGGGCAGATCACTT GCTGGGTGTGGTGGCTCATGCCTGTAATCCCAGCATTTTGGGAGGCTGAGGTGGGCAGATCACTT T C BAZ1A Ensembl:ENSG00000198604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1287612300 Functional Loss SNV dbSNP153 33..33 33 - - - 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_372304,RMVar_hsa_circ_87745,RMVar_hsa_circ_111427,RMVar_hsa_circ_165891,RMVar_hsa_circ_65146,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_296823,RMVar_hsa_circ_165895,RMVar_hsa_circ_165896,RMVar_hsa_circ_365963,RMVar_hsa_circ_165898,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_273898,RMVar_hsa_circ_52749,RMVar_hsa_circ_111170,RMVar_hsa_circ_165903,RMVar_hsa_circ_165904,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_165905 25692 RMVar_ID_25692 Human_SNP_ID_550826187 A-to-I Human chr14 - 34801469 34801469 34801469 CAACATGGCAAAACCCTGTATCTACTAAAAATACAAAAAAAAATTAGCCAGGTGTGGTGGCACAT CAACATGGCAAAACCCTGTATCTACTAAAAATGCAAAAAAAAATTAGCCAGGTGTGGTGGCACAT T C BAZ1A Ensembl:ENSG00000198604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1413929241 Functional Loss SNV dbSNP153 33..33 33 - - - 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_365280,RMVar_hsa_circ_312292,RMVar_hsa_circ_165911,RMVar_hsa_circ_165910,RMVar_hsa_circ_26241,RMVar_hsa_circ_113341,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,RMVar_hsa_circ_165915,RMVar_hsa_circ_368798,RMVar_hsa_circ_371250,RMVar_hsa_circ_65836 25693 RMVar_ID_25693 Human_SNP_ID_550826230 A-to-I Human chr14 - 34801663 34801663 34801663 CTCAAGTATTCTACCCGCCGTGGCTTCCCAAAATGCTAGGATCACAGGCATGAGCCACTGTGCCC CTCAAGTATTCTACCCGCCGTGGCTTCCCAAAGTGCTAGGATCACAGGCATGAGCCACTGTGCCC T C BAZ1A Ensembl:ENSG00000198604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs766117613 Functional Loss SNV dbSNP153 33..33 33 - - - 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_365280,RMVar_hsa_circ_312292,RMVar_hsa_circ_165911,RMVar_hsa_circ_165910,RMVar_hsa_circ_26241,RMVar_hsa_circ_113341,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,RMVar_hsa_circ_165915,RMVar_hsa_circ_368798,RMVar_hsa_circ_371250,RMVar_hsa_circ_65836 25694 RMVar_ID_25694 Human_SNP_ID_550826248 A-to-I Human chr14 - 34801706 34801706 34801706 TGGGGTTTCACCATGTTGGCCAGGCTGCTCTCAAACGCCCGACCTCAAGTATTCTACCCGCCGTG TGGGGTTTCACCATGTTGGCCAGGCTGCTCTCGAACGCCCGACCTCAAGTATTCTACCCGCCGTG T C BAZ1A Ensembl:ENSG00000198604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1174558229 Functional Loss SNV dbSNP153 33..33 33 - - - 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_365280,RMVar_hsa_circ_312292,RMVar_hsa_circ_165911,RMVar_hsa_circ_165910,RMVar_hsa_circ_26241,RMVar_hsa_circ_113341,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,RMVar_hsa_circ_165915,RMVar_hsa_circ_368798,RMVar_hsa_circ_371250,RMVar_hsa_circ_65836 25695 RMVar_ID_25695 Human_SNP_ID_550826254 A-to-I Human chr14 - 34801743 34801743 34801743 CACCACGCCCAGCTAATTTTTGCATTTTTAATAGAGATGGGGTTTCACCATGTTGGCCAGGCTGC CACCACGCCCAGCTAATTTTTGCATTTTTAATGGAGATGGGGTTTCACCATGTTGGCCAGGCTGC T C BAZ1A Ensembl:ENSG00000198604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1007731782 Functional Loss SNV dbSNP153 33..33 33 - - - 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_365280,RMVar_hsa_circ_312292,RMVar_hsa_circ_165911,RMVar_hsa_circ_165910,RMVar_hsa_circ_26241,RMVar_hsa_circ_113341,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,RMVar_hsa_circ_165915,RMVar_hsa_circ_368798,RMVar_hsa_circ_371250,RMVar_hsa_circ_65836 25696 RMVar_ID_25696 Human_SNP_ID_550830289 A-to-I Human chr14 - 34819432 34819432 34819432 AAAGTCTACATACTTATGATTCCAACTATGACATTCTGGAAAAGGCACAGCTATGGAGACAGTAA AAAGTCTACATACTTATGATTCCAACTATGACGTTCTGGAAAAGGCACAGCTATGGAGACAGTAA T C BAZ1A Ensembl:ENSG00000198604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10131094 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8403170 GWAS_ID_2445,GWAS_ID_2446,GWAS_ID_2447,GWAS_ID_2448,GWAS_ID_2449,GWAS_ID_2450,GWAS_ID_2451,GWAS_ID_2452,GWAS_ID_2453,GWAS_ID_2454,GWAS_ID_2455,GWAS_ID_2456,GWAS_ID_2457,GWAS_ID_2458,GWAS_ID_2459,GWAS_ID_2460,GWAS_ID_2461,GWAS_ID_2462,GWAS_ID_2463,GWAS_ID_2464,GWAS_ID_2465,GWAS_ID_2466,GWAS_ID_2467,GWAS_ID_2468,GWAS_ID_2469,GWAS_ID_2470,GWAS_ID_2471,GWAS_ID_2472,GWAS_ID_2473,GWAS_ID_2474,GWAS_ID_2475,GWAS_ID_2476,GWAS_ID_2477,GWAS_ID_2478,GWAS_ID_2479,GWAS_ID_2480,GWAS_ID_2481,GWAS_ID_2482,GWAS_ID_2483,GWAS_ID_2484,GWAS_ID_2485,GWAS_ID_2486,GWAS_ID_2487,GWAS_ID_2488,GWAS_ID_2489,GWAS_ID_2490,GWAS_ID_2491,GWAS_ID_2492,GWAS_ID_2493,GWAS_ID_2494,GWAS_ID_2495,GWAS_ID_2496,GWAS_ID_2497,GWAS_ID_2498,GWAS_ID_2499,GWAS_ID_2500,GWAS_ID_2501,GWAS_ID_2502,GWAS_ID_2503,GWAS_ID_2504,GWAS_ID_2505,GWAS_ID_2506,GWAS_ID_2507,GWAS_ID_2508,GWAS_ID_2509,GWAS_ID_2510,GWAS_ID_2511,GWAS_ID_2512,GWAS_ID_2513,GWAS_ID_2514,GWAS_ID_2515,GWAS_ID_2516,GWAS_ID_2517,GWAS_ID_2518,GWAS_ID_2519,GWAS_ID_2520,GWAS_ID_2521,GWAS_ID_2522,GWAS_ID_2523,GWAS_ID_2524,GWAS_ID_2525,GWAS_ID_2526,GWAS_ID_2527,GWAS_ID_2528,GWAS_ID_2529,GWAS_ID_2530,GWAS_ID_2531,GWAS_ID_2532,GWAS_ID_2533,GWAS_ID_2534,GWAS_ID_2535,GWAS_ID_2536,GWAS_ID_2537,GWAS_ID_2538,GWAS_ID_2539,GWAS_ID_2540 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_303659,RMVar_hsa_circ_111170,RMVar_hsa_circ_165905,RMVar_hsa_circ_165909,RMVar_hsa_circ_264933,RMVar_hsa_circ_365280,RMVar_hsa_circ_165911,RMVar_hsa_circ_165910,RMVar_hsa_circ_113341,RMVar_hsa_circ_332865,RMVar_hsa_circ_69834,RMVar_hsa_circ_165914,RMVar_hsa_circ_165915,RMVar_hsa_circ_371250,RMVar_hsa_circ_374486,RMVar_hsa_circ_165919,RMVar_hsa_circ_165916,RMVar_hsa_circ_314991,RMVar_hsa_circ_315668,RMVar_hsa_circ_165920,RMVar_hsa_circ_165922,RMVar_hsa_circ_340492,RMVar_hsa_circ_343752 25697 RMVar_ID_25697 Human_SNP_ID_550830533 A-to-I Human chr14 - 34820264 34820264 34820264 AAAATCAGCCGGGTATTGTGGTGTGTGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGTGGGAGG AAAATCAGCCGGGTATTGTGGTGTGTGCCTGTGGTCCCAGCTACTCGGGAGGCTGAGGTGGGAGG T C BAZ1A Ensembl:ENSG00000198604 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1244867454 Functional Loss SNV dbSNP153 33..33 33 - - - 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_303659,RMVar_hsa_circ_111170,RMVar_hsa_circ_165905,RMVar_hsa_circ_165909,RMVar_hsa_circ_264933,RMVar_hsa_circ_365280,RMVar_hsa_circ_165911,RMVar_hsa_circ_165910,RMVar_hsa_circ_113341,RMVar_hsa_circ_332865,RMVar_hsa_circ_69834,RMVar_hsa_circ_165914,RMVar_hsa_circ_165915,RMVar_hsa_circ_371250,RMVar_hsa_circ_374486,RMVar_hsa_circ_165919,RMVar_hsa_circ_165916,RMVar_hsa_circ_314991,RMVar_hsa_circ_315668,RMVar_hsa_circ_165920,RMVar_hsa_circ_165922,RMVar_hsa_circ_340492,RMVar_hsa_circ_343752 25698 RMVar_ID_25698 Human_SNP_ID_550840141 A-to-I Human chr14 - 34858395 34858395 34858395 AGTAGTCAATAGTCAATTACAGGCATGTGCCTATAATTCCAGTTACTCAGGAGGCTGAGGCAGAA AGTAGTCAATAGTCAATTACAGGCATGTGCCTGTAATTCCAGTTACTCAGGAGGCTGAGGCAGAA T C BAZ1A Ensembl:ENSG00000198604 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1293553623 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83760,RMVar_hsa_circ_165890,RMVar_hsa_circ_165892,RMVar_hsa_circ_87745,RMVar_hsa_circ_111427,RMVar_hsa_circ_120786,RMVar_hsa_circ_165893,RMVar_hsa_circ_372223,RMVar_hsa_circ_165894,RMVar_hsa_circ_165895,RMVar_hsa_circ_115563,RMVar_hsa_circ_165902,RMVar_hsa_circ_303659,RMVar_hsa_circ_111170,RMVar_hsa_circ_165905,RMVar_hsa_circ_165909,RMVar_hsa_circ_264933,RMVar_hsa_circ_365280,RMVar_hsa_circ_165911,RMVar_hsa_circ_165910,RMVar_hsa_circ_113341,RMVar_hsa_circ_332865,RMVar_hsa_circ_165914,RMVar_hsa_circ_165915,RMVar_hsa_circ_371250,RMVar_hsa_circ_374486,RMVar_hsa_circ_165916,RMVar_hsa_circ_314991,RMVar_hsa_circ_165920,RMVar_hsa_circ_165922,RMVar_hsa_circ_340492,RMVar_hsa_circ_294174,RMVar_hsa_circ_283574,RMVar_hsa_circ_165924 25699 RMVar_ID_25699 Human_SNP_ID_550841051 A-to-I Human chr14 - 34862150 34862150 34862150 TAATTATTCCAGTTTTATACTTGACCAGCCTTACCCATCGTTCGCGCTTACATGAAATTTGTGAT TAATTATTCCAGTTTTATACTTGACCAGCCTTTCCCATCGTTCGCGCTTACATGAAATTTGTGAT T A BAZ1A Ensembl:ENSG00000198604 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs771695338 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8794386,Human_RBP_ID_12320951,Human_RBP_ID_26923841,Human_RBP_ID_27226451,Human_RBP_ID_27808216 RMVar_hsa_circ_83760,RMVar_hsa_circ_165890,RMVar_hsa_circ_165892,RMVar_hsa_circ_87745,RMVar_hsa_circ_111427,RMVar_hsa_circ_120786,RMVar_hsa_circ_165893,RMVar_hsa_circ_372223,RMVar_hsa_circ_165894,RMVar_hsa_circ_165895,RMVar_hsa_circ_115563,RMVar_hsa_circ_165902,RMVar_hsa_circ_303659,RMVar_hsa_circ_111170,RMVar_hsa_circ_165905,RMVar_hsa_circ_165909,RMVar_hsa_circ_264933,RMVar_hsa_circ_365280,RMVar_hsa_circ_165911,RMVar_hsa_circ_165910,RMVar_hsa_circ_113341,RMVar_hsa_circ_332865,RMVar_hsa_circ_165914,RMVar_hsa_circ_165915,RMVar_hsa_circ_371250,RMVar_hsa_circ_374486,RMVar_hsa_circ_165916,RMVar_hsa_circ_314991,RMVar_hsa_circ_165920,RMVar_hsa_circ_165922,RMVar_hsa_circ_340492,RMVar_hsa_circ_294174,RMVar_hsa_circ_283574,RMVar_hsa_circ_165926,RMVar_hsa_circ_165924,RMVar_hsa_circ_115780,RMVar_hsa_circ_273155,RMVar_hsa_circ_165925 25700 RMVar_ID_25700 Human_SNP_ID_550861097 A-to-I Human chr14 + 34940129 34940129 34940129 GTCTGGCAACTATGACGGTGAGTGACTGGTATAAGCAACATTGGAAATATGGAGCATTACCAGAT GTCTGGCAACTATGACGGTGAGTGACTGGTATGAGCAACATTGGAAATATGGAGCATTACCAGAT A G IGBP1P1 Ensembl:ENSG00000226677 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879180402 Functional Loss SNV dbSNP153 33..33 33 - - - 25701 RMVar_ID_25701 Human_SNP_ID_550861105 A-to-I Human chr14 + 34940158 34940158 34940158 TATAAGCAACATTGGAAATATGGAGCATTACCAGATCAGGGAATAGCCAAGGCAACACCAGAGGA TATAAGCAACATTGGAAATATGGAGCATTACCGGATCAGGGAATAGCCAAGGCAACACCAGAGGA A G IGBP1P1 Ensembl:ENSG00000226677 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879031614 Functional Loss SNV dbSNP153 33..33 33 - - - 25702 RMVar_ID_25702 Human_SNP_ID_550863107 A-to-I Human chr14 - 34948556 34948556 34948556 CACCTGCCTTTGCCTCCCAAAATGCTGAGATTACAAGTATGAGGCACCACTCCTGGCTTAATTTT CACCTGCCTTTGCCTCCCAAAATGCTGAGATTGCAAGTATGAGGCACCACTCCTGGCTTAATTTT T C SRP54-AS1 Ensembl:ENSG00000258704 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs988832721 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_165927,RMVar_hsa_circ_165929,RMVar_hsa_circ_24484 25703 RMVar_ID_25703 Human_SNP_ID_550863947 A-to-I Human chr14 - 34951795 34951795 34951795 TAGTAGCTGGGACTACAGGTGTGCGTCACCACACCCAGCTGATTTTTTTGGATTTTTAGTAGAGA TAGTAGCTGGGACTACAGGTGTGCGTCACCACTCCCAGCTGATTTTTTTGGATTTTTAGTAGAGA T A SRP54-AS1 Ensembl:ENSG00000258704 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1489572910 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_165927,RMVar_hsa_circ_165929,RMVar_hsa_circ_24484 25704 RMVar_ID_25704 Human_SNP_ID_550863948 A-to-I Human chr14 - 34951795 34951795 34951795 TAGTAGCTGGGACTACAGGTGTGCGTCACCACACCCAGCTGATTTTTTTGGATTTTTAGTAGAGA TAGTAGCTGGGACTACAGGTGTGCGTCACCACGCCCAGCTGATTTTTTTGGATTTTTAGTAGAGA T C SRP54-AS1 Ensembl:ENSG00000258704 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1489572910 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_165927,RMVar_hsa_circ_165929,RMVar_hsa_circ_24484 25705 RMVar_ID_25705 Human_SNP_ID_550863964 A-to-I Human chr14 - 34951866 34951866 34951866 CAGTAGCGTAATCTTGGCTCACTGTAACCTCAACCTCCCGGGTACAAGCGATTCTCCTGCCTCAG CAGTAGCGTAATCTTGGCTCACTGTAACCTCAGCCTCCCGGGTACAAGCGATTCTCCTGCCTCAG T C SRP54-AS1 Ensembl:ENSG00000258704 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1021790652 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17364107 RMVar_hsa_circ_165927,RMVar_hsa_circ_165929,RMVar_hsa_circ_24484 25706 RMVar_ID_25706 Human_SNP_ID_550863973 A-to-I Human chr14 - 34951894 34951894 34951894 GTCTCCCTCTGTAGCCCATGCTGGAGTGCAGTAGCGTAATCTTGGCTCACTGTAACCTCAACCTC GTCTCCCTCTGTAGCCCATGCTGGAGTGCAGTGGCGTAATCTTGGCTCACTGTAACCTCAACCTC T C SRP54-AS1 Ensembl:ENSG00000258704 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1035345176 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_165927,RMVar_hsa_circ_165929,RMVar_hsa_circ_24484 25707 RMVar_ID_25707 Human_SNP_ID_550864636 A-to-I Human chr14 - 34954548 34954548 34954548 GCGATCTTAGCTCACTGCAACCGCCACATCCCAGGTTCAAGCAATTCTCCCACCTCAGCCTTCCA GCGATCTTAGCTCACTGCAACCGCCACATCCCGGGTTCAAGCAATTCTCCCACCTCAGCCTTCCA T C SRP54-AS1 Ensembl:ENSG00000258704 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1013521153 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_165927,RMVar_hsa_circ_165929,RMVar_hsa_circ_24484 25708 RMVar_ID_25708 Human_SNP_ID_550866494 A-to-I Human chr14 - 34961802 34961802 34961802 AATTAGTCAGGTGTGGTGGCGCCTGCCCTGTAATCCCAGCTACTTGGGAGACAGAAGCAGGAGAA AATTAGTCAGGTGTGGTGGCGCCTGCCCTGTAGTCCCAGCTACTTGGGAGACAGAAGCAGGAGAA T C SRP54-AS1 Ensembl:ENSG00000258704 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs764212830 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_165927,RMVar_hsa_circ_165929,RMVar_hsa_circ_24484,RMVar_hsa_circ_338574 25709 RMVar_ID_25709 Human_SNP_ID_550866531 A-to-I Human chr14 - 34961945 34961945 34961945 ATAAAAACTCTGAGGCTGGCCTGGTGGCTTACACCTGTAATTCCAGCACTTTGGGAGACCAAGGC ATAAAAACTCTGAGGCTGGCCTGGTGGCTTACGCCTGTAATTCCAGCACTTTGGGAGACCAAGGC T C SRP54-AS1 Ensembl:ENSG00000258704 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965769339 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_165927,RMVar_hsa_circ_165929,RMVar_hsa_circ_24484,RMVar_hsa_circ_338574 25710 RMVar_ID_25710 Human_SNP_ID_550866734 A-to-I Human chr14 - 34962637 34962636 34962638 TTGAGATGGAGTGTCACTCTGTCACCCTGACTAGAGTGCAGTGGCACGATCTCGGCTCACTGAAA TTGAGATGGAGTGTCACTCTGTCACCCTGAC__GAGTGCAGTGGCACGATCTCGGCTCACTGAAA CTA C SRP54-AS1 Ensembl:ENSG00000258704 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1456559465 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_165927,RMVar_hsa_circ_165929,RMVar_hsa_circ_24484,RMVar_hsa_circ_338574 25711 RMVar_ID_25711 Human_SNP_ID_550866735 A-to-I Human chr14 - 34962637 34962637 34962637 TTGAGATGGAGTGTCACTCTGTCACCCTGACTAGAGTGCAGTGGCACGATCTCGGCTCACTGAAA TTGAGATGGAGTGTCACTCTGTCACCCTGACTGGAGTGCAGTGGCACGATCTCGGCTCACTGAAA T C SRP54-AS1 Ensembl:ENSG00000258704 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388640736 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_165927,RMVar_hsa_circ_165929,RMVar_hsa_circ_24484,RMVar_hsa_circ_338574 25712 RMVar_ID_25712 Human_SNP_ID_550868163 A-to-I Human chr14 - 34968373 34968373 34968373 TACTTGAGCTGGGCATGGTGGTGTGTACCTGTAGTCCCAGCTACTTGGGAGGCTGAGGTGGAAGG TACTTGAGCTGGGCATGGTGGTGTGTACCTGTGGTCCCAGCTACTTGGGAGGCTGAGGTGGAAGG T C SRP54-AS1 Ensembl:ENSG00000258704 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1400490440 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5246806,Human_RBP_ID_17562883 RMVar_hsa_circ_165927,RMVar_hsa_circ_165929,RMVar_hsa_circ_75343,RMVar_hsa_circ_24484,RMVar_hsa_circ_338574,RMVar_hsa_circ_165932 25713 RMVar_ID_25713 Human_SNP_ID_550868259 A-to-I Human chr14 - 34968811 34968808 34968811 ATTGTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCACCCGCCACCACACCTAGCTAATTTTT ATTGTGCCTCAGCCTCCCAAGTAGCTGGGATT___GGCACCCGCCACCACACCTAGCTAATTTTT CTGT C SRP54-AS1 Ensembl:ENSG00000258704 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1160568097 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_165927,RMVar_hsa_circ_165929,RMVar_hsa_circ_75343,RMVar_hsa_circ_24484,RMVar_hsa_circ_338574,RMVar_hsa_circ_165932 25714 RMVar_ID_25714 Human_SNP_ID_550869449 A-to-I Human chr14 - 34973670 34973670 34973670 TCAGCCTCCCAGGTAGCTGGGACTATAGGCATACACCACCATGCCCAGCTACTTTTTAATTTTTT TCAGCCTCCCAGGTAGCTGGGACTATAGGCATTCACCACCATGCCCAGCTACTTTTTAATTTTTT T A SRP54-AS1 Ensembl:ENSG00000258704 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1469569782 Functional Loss SNV dbSNP153 33..33 33 - - - 25715 RMVar_ID_25715 Human_SNP_ID_550870693 A-to-I Human chr14 - 34978334 34978334 34978334 CTTCAGACAGAGTCTTGCTCTTTGCCCAGGCTAGAGTGCAATGGCACAATCTCGGCTCACTGCAA CTTCAGACAGAGTCTTGCTCTTTGCCCAGGCTGGAGTGCAATGGCACAATCTCGGCTCACTGCAA T C SRP54-AS1 Ensembl:ENSG00000258704 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs780710145 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5246813 25716 RMVar_ID_25716 Human_SNP_ID_550878205 A-to-I Human chr14 + 35003508 35003508 35003508 GCGATCTTCTCTCCTCAGCCTCCAGAGAAGCTAGGACTACAGGCATGCACCACCATGTTTTTTGT GCGATCTTCTCTCCTCAGCCTCCAGAGAAGCTGGGACTACAGGCATGCACCACCATGTTTTTTGT A G SRP54 Ensembl:ENSG00000100883 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1234115796 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6343125 RMVar_hsa_circ_45420,RMVar_hsa_circ_55979,RMVar_hsa_circ_350925,RMVar_hsa_circ_58999,RMVar_hsa_circ_33222,RMVar_hsa_circ_165936,RMVar_hsa_circ_165938,RMVar_hsa_circ_270204,RMVar_hsa_circ_313315,RMVar_hsa_circ_328374,RMVar_hsa_circ_342242,RMVar_hsa_circ_293811,RMVar_hsa_circ_56476,RMVar_hsa_circ_63337,RMVar_hsa_circ_165939,RMVar_hsa_circ_165940,RMVar_hsa_circ_165937 25717 RMVar_ID_25717 Human_SNP_ID_550878606 A-to-I Human chr14 + 35005131 35005131 35005131 AGGCTGGAGGATTACTTGAGGCCAAGAGTTCAAAACCAGTCTGGGCAACATAGCAATACTCCATC AGGCTGGAGGATTACTTGAGGCCAAGAGTTCAGAACCAGTCTGGGCAACATAGCAATACTCCATC A G SRP54 Ensembl:ENSG00000100883 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1410180735 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45420,RMVar_hsa_circ_55979,RMVar_hsa_circ_350925,RMVar_hsa_circ_58999,RMVar_hsa_circ_33222,RMVar_hsa_circ_165936,RMVar_hsa_circ_165938,RMVar_hsa_circ_270204,RMVar_hsa_circ_313315,RMVar_hsa_circ_328374,RMVar_hsa_circ_342242,RMVar_hsa_circ_293811,RMVar_hsa_circ_56476,RMVar_hsa_circ_63337,RMVar_hsa_circ_165939,RMVar_hsa_circ_165940,RMVar_hsa_circ_165937 25718 RMVar_ID_25718 Human_SNP_ID_550878695 A-to-I Human chr14 + 35005514 35005514 35005514 AAACTCCTGGGCTCAAGCAATCTTACTGCCTCAGCCTCCTTGATTAGCTGGGACCACAGGTGCGT AAACTCCTGGGCTCAAGCAATCTTACTGCCTCGGCCTCCTTGATTAGCTGGGACCACAGGTGCGT A G SRP54 Ensembl:ENSG00000100883 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1204258858 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17562241 RMVar_hsa_circ_45420,RMVar_hsa_circ_55979,RMVar_hsa_circ_350925,RMVar_hsa_circ_58999,RMVar_hsa_circ_33222,RMVar_hsa_circ_165936,RMVar_hsa_circ_165938,RMVar_hsa_circ_270204,RMVar_hsa_circ_313315,RMVar_hsa_circ_328374,RMVar_hsa_circ_342242,RMVar_hsa_circ_293811,RMVar_hsa_circ_56476,RMVar_hsa_circ_63337,RMVar_hsa_circ_165939,RMVar_hsa_circ_165940,RMVar_hsa_circ_165937 25719 RMVar_ID_25719 Human_SNP_ID_550878717 A-to-I Human chr14 + 35005596 35005596 35005596 ATTCTTTAAATTAGTAGAGACAAGATCTTGCTATGCTGCCCAAGCTGGTCTCAAACTCCTGGTCT ATTCTTTAAATTAGTAGAGACAAGATCTTGCTGTGCTGCCCAAGCTGGTCTCAAACTCCTGGTCT A G SRP54 Ensembl:ENSG00000100883 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs968302673 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17562457 RMVar_hsa_circ_45420,RMVar_hsa_circ_55979,RMVar_hsa_circ_350925,RMVar_hsa_circ_58999,RMVar_hsa_circ_33222,RMVar_hsa_circ_165936,RMVar_hsa_circ_165938,RMVar_hsa_circ_270204,RMVar_hsa_circ_313315,RMVar_hsa_circ_328374,RMVar_hsa_circ_342242,RMVar_hsa_circ_293811,RMVar_hsa_circ_56476,RMVar_hsa_circ_63337,RMVar_hsa_circ_165939,RMVar_hsa_circ_165940,RMVar_hsa_circ_165937 25720 RMVar_ID_25720 Human_SNP_ID_550879083 A-to-I Human chr14 + 35007050 35007050 35007050 GTCTCTACAAAAAAAAATTTTTTTAGTTAACTAGGTGTGGTGGCGTGTGCCTGTAGTCCCAGTTA GTCTCTACAAAAAAAAATTTTTTTAGTTAACTCGGTGTGGTGGCGTGTGCCTGTAGTCCCAGTTA A C SRP54 Ensembl:ENSG00000100883 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1030923704 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45420,RMVar_hsa_circ_55979,RMVar_hsa_circ_350925,RMVar_hsa_circ_58999,RMVar_hsa_circ_33222,RMVar_hsa_circ_165936,RMVar_hsa_circ_165938,RMVar_hsa_circ_270204,RMVar_hsa_circ_313315,RMVar_hsa_circ_328374,RMVar_hsa_circ_342242,RMVar_hsa_circ_293811,RMVar_hsa_circ_56476,RMVar_hsa_circ_63337,RMVar_hsa_circ_165939,RMVar_hsa_circ_165940,RMVar_hsa_circ_165937 25721 RMVar_ID_25721 Human_SNP_ID_550879084 A-to-I Human chr14 + 35007050 35007050 35007050 GTCTCTACAAAAAAAAATTTTTTTAGTTAACTAGGTGTGGTGGCGTGTGCCTGTAGTCCCAGTTA GTCTCTACAAAAAAAAATTTTTTTAGTTAACTTGGTGTGGTGGCGTGTGCCTGTAGTCCCAGTTA A T SRP54 Ensembl:ENSG00000100883 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1030923704 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45420,RMVar_hsa_circ_55979,RMVar_hsa_circ_350925,RMVar_hsa_circ_58999,RMVar_hsa_circ_33222,RMVar_hsa_circ_165936,RMVar_hsa_circ_165938,RMVar_hsa_circ_270204,RMVar_hsa_circ_313315,RMVar_hsa_circ_328374,RMVar_hsa_circ_342242,RMVar_hsa_circ_293811,RMVar_hsa_circ_56476,RMVar_hsa_circ_63337,RMVar_hsa_circ_165939,RMVar_hsa_circ_165940,RMVar_hsa_circ_165937 25722 RMVar_ID_25722 Human_SNP_ID_550882976 A-to-I Human chr14 + 35021374 35021374 35021374 AAAGCTGGCCAGGTGCGGTGGCTCTCAACTGTAATCCCAGCATTTTGGGAGGCTGAGGTCGGTGG AAAGCTGGCCAGGTGCGGTGGCTCTCAACTGTCATCCCAGCATTTTGGGAGGCTGAGGTCGGTGG A C SRP54 Ensembl:ENSG00000100883 Protein coding intron GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-Seq:(High) rs1204148739 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56476,RMVar_hsa_circ_352565 25723 RMVar_ID_25723 Human_SNP_ID_550883027 A-to-I Human chr14 + 35021620 35021620 35021620 GCACCACTGCACTCCAGCCTGAGGGACAGAGCAACACTCTGTCTCAAAAAAAAAAAAGATTTTGA GCACCACTGCACTCCAGCCTGAGGGACAGAGCGACACTCTGTCTCAAAAAAAAAAAAGATTTTGA A G SRP54 Ensembl:ENSG00000100883 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1298515646 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17562459 RMVar_hsa_circ_56476,RMVar_hsa_circ_352565 25724 RMVar_ID_25724 Human_SNP_ID_550883577 A-to-I Human chr14 + 35023673 35023673 35023673 GGGTGTCGTGGGGTGTACCTGTTATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAA GGGTGTCGTGGGGTGTACCTGTTATCCCAGCTGCTCGGGAGGCTGAGGCAGGAGAATCACTTGAA A G SRP54 Ensembl:ENSG00000100883 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs979380010 Functional Loss SNV dbSNP153 33..33 33 - - - 25725 RMVar_ID_25725 Human_SNP_ID_550883578 A-to-I Human chr14 + 35023673 35023673 35023673 GGGTGTCGTGGGGTGTACCTGTTATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAA GGGTGTCGTGGGGTGTACCTGTTATCCCAGCTTCTCGGGAGGCTGAGGCAGGAGAATCACTTGAA A T SRP54 Ensembl:ENSG00000100883 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs979380010 Functional Loss SNV dbSNP153 33..33 33 - - - 25726 RMVar_ID_25726 Human_SNP_ID_550883753 A-to-I Human chr14 + 35024238 35024238 35024238 TTTAGTAGAGACGGGGTTTCACTATGTTGGCCAGGCTGGTCTTGAACTCCTGACCTCAAATGATG TTTAGTAGAGACGGGGTTTCACTATGTTGGCCGGGCTGGTCTTGAACTCCTGACCTCAAATGATG A G SRP54 Ensembl:ENSG00000100883 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1164743896 Functional Loss SNV dbSNP153 33..33 33 - - - 25727 RMVar_ID_25727 Human_SNP_ID_550883886 A-to-I Human chr14 + 35024752 35024752 35024752 GTTGTCACCATTTTCTTCTTTTTTTGAGACAGAGTCTTGCTCTGTCGCCCAGGCTGGAGTGCACT GTTGTCACCATTTTCTTCTTTTTTTGAGACAGGGTCTTGCTCTGTCGCCCAGGCTGGAGTGCACT A G SRP54 Ensembl:ENSG00000100883 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs536820189 Functional Loss SNV dbSNP153 33..33 33 - - - 25728 RMVar_ID_25728 Human_SNP_ID_550883887 A-to-I Human chr14 + 35024752 35024752 35024752 GTTGTCACCATTTTCTTCTTTTTTTGAGACAGAGTCTTGCTCTGTCGCCCAGGCTGGAGTGCACT GTTGTCACCATTTTCTTCTTTTTTTGAGACAGTGTCTTGCTCTGTCGCCCAGGCTGGAGTGCACT A T SRP54 Ensembl:ENSG00000100883 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs536820189 Functional Loss SNV dbSNP153 33..33 33 - - - 25729 RMVar_ID_25729 Human_SNP_ID_550883903 A-to-I Human chr14 + 35024844 35024844 35024844 CGCCTCCTGGGTTCAAGCTATTCTCCTGCCTCAGTCTCCCGAGTAGCTGGGATTTCAAGCACGTG CGCCTCCTGGGTTCAAGCTATTCTCCTGCCTCGGTCTCCCGAGTAGCTGGGATTTCAAGCACGTG A G SRP54 Ensembl:ENSG00000100883 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1214663984 Functional Loss SNV dbSNP153 33..33 33 - - - 25730 RMVar_ID_25730 Human_SNP_ID_550884240 A-to-I Human chr14 + 35026244 35026243 35026245 TTTTGTTTGTTTGTTTTGTTTTGTTTTGAGACAGGGTCTCGCTGTGTCACCCAGGCTGGGGGCTG TTTTGTTTGTTTGTTTTGTTTTGTTTTGAGAC__GGTCTCGCTGTGTCACCCAGGCTGGGGGCTG CAG C SRP54 Ensembl:ENSG00000100883 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1246927889 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_1084966,Human_RBP_ID_17562460 25731 RMVar_ID_25731 Human_SNP_ID_550884248 A-to-I Human chr14 + 35026289 35026289 35026289 GTCACCCAGGCTGGGGGCTGAAGTGCAATGGCATGATCATGGCTCACTGCAGCCTTGACCTCCCA GTCACCCAGGCTGGGGGCTGAAGTGCAATGGCGTGATCATGGCTCACTGCAGCCTTGACCTCCCA A G SRP54 Ensembl:ENSG00000100883 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1420110023 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17562460 25732 RMVar_ID_25732 Human_SNP_ID_550884270 A-to-I Human chr14 + 35026362 35026362 35026362 CGATCCTCCAATCTGAGGCCCCCAAGTAGCTGAGACTACAGACGCATGCTATCACACTGAGCTAA CGATCCTCCAATCTGAGGCCCCCAAGTAGCTGCGACTACAGACGCATGCTATCACACTGAGCTAA A C SRP54 Ensembl:ENSG00000100883 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,31158229,32596459 RNA-Seq:(High) rs1433925153 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12321838 25733 RMVar_ID_25733 Human_SNP_ID_550884310 A-to-I Human chr14 + 35026472 35026472 35026472 CCCAGGCTGATCTTGAACTCCTGGGCTCAAGTAATCAGCCTACCTTCGCCACCTGAAGTGCTGGG CCCAGGCTGATCTTGAACTCCTGGGCTCAAGTCATCAGCCTACCTTCGCCACCTGAAGTGCTGGG A C SRP54 Ensembl:ENSG00000100883 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs965263620 Functional Loss SNV dbSNP153 33..33 33 - - - 25734 RMVar_ID_25734 Human_SNP_ID_550884313 A-to-I Human chr14 + 35026481 35026481 35026481 ATCTTGAACTCCTGGGCTCAAGTAATCAGCCTACCTTCGCCACCTGAAGTGCTGGGATTACAAAT ATCTTGAACTCCTGGGCTCAAGTAATCAGCCTGCCTTCGCCACCTGAAGTGCTGGGATTACAAAT A G SRP54 Ensembl:ENSG00000100883 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs367818122 Functional Loss SNV dbSNP153 33..33 33 - - - 25735 RMVar_ID_25735 Human_SNP_ID_550884421 A-to-I Human chr14 + 35026938 35026938 35026938 GCACTCCAGCCTGGGTGACAGAGCTAGACTCCATCTCAAAAACAAAACAAAACAAAAAAAACTTC GCACTCCAGCCTGGGTGACAGAGCTAGACTCCGTCTCAAAAACAAAACAAAACAAAAAAAACTTC A G SRP54 Ensembl:ENSG00000100883 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs377251327 Functional Loss SNV dbSNP153 33..33 33 - - - 25736 RMVar_ID_25736 Human_SNP_ID_550884422 A-to-I Human chr14 + 35026938 35026938 35026938 GCACTCCAGCCTGGGTGACAGAGCTAGACTCCATCTCAAAAACAAAACAAAACAAAAAAAACTTC GCACTCCAGCCTGGGTGACAGAGCTAGACTCCTTCTCAAAAACAAAACAAAACAAAAAAAACTTC A T SRP54 Ensembl:ENSG00000100883 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs377251327 Functional Loss SNV dbSNP153 33..33 33 - - - 25737 RMVar_ID_25737 Human_SNP_ID_550884605 A-to-I Human chr14 + 35027502 35027502 35027502 CTGGCTGACCAGGTACGGTGTCTCACACCTGTAATCCCAGCACTCTGGGAGGCTGAGGTGAGTGG CTGGCTGACCAGGTACGGTGTCTCACACCTGTGATCCCAGCACTCTGGGAGGCTGAGGTGAGTGG A G SRP54 Ensembl:ENSG00000100883 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs960156942 Functional Loss SNV dbSNP153 33..33 33 - - - 25738 RMVar_ID_25738 Human_SNP_ID_550890711 A-to-I Human chr14 + 35050027 35050027 35050027 AAAATTCACAGTGTAACTTTTTTTGTTTTTTGAGACAGAATCTCACTCTGTTGCCCAGGCTGAAG AAAATTCACAGTGTAACTTTTTTTGTTTTTTGCGACAGAATCTCACTCTGTTGCCCAGGCTGAAG A C FAM177A1 Ensembl:ENSG00000151327 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs542634600 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_30378,RMVar_hsa_circ_104366,RMVar_hsa_circ_165948,RMVar_hsa_circ_313160 25739 RMVar_ID_25739 Human_SNP_ID_550890767 A-to-I Human chr14 + 35050192 35050192 35050192 CCGCGCCTGGCTAATTTTTGTATTTTTTTAGTAGAGGTGGGATTTCACCATGTTAGCCAGGGTGG CCGCGCCTGGCTAATTTTTGTATTTTTTTAGTGGAGGTGGGATTTCACCATGTTAGCCAGGGTGG A G FAM177A1 Ensembl:ENSG00000151327 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1020310488 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8403217,Human_RBP_ID_9324038,Human_RBP_ID_21886713 RMVar_hsa_circ_30378,RMVar_hsa_circ_104366,RMVar_hsa_circ_165948,RMVar_hsa_circ_313160 25740 RMVar_ID_25740 Human_SNP_ID_550890779 A-to-I Human chr14 + 35050214 35050214 35050214 TTTTTTTAGTAGAGGTGGGATTTCACCATGTTAGCCAGGGTGGTCTCACACCCTTGACCTCAAGT TTTTTTTAGTAGAGGTGGGATTTCACCATGTTGGCCAGGGTGGTCTCACACCCTTGACCTCAAGT A G FAM177A1 Ensembl:ENSG00000151327 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 29129909,30559470 RNA-Seq:(High) rs937496023 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8403217,Human_RBP_ID_9324038,Human_RBP_ID_21886713,Human_RBP_ID_24410881 RMVar_hsa_circ_30378,RMVar_hsa_circ_104366,RMVar_hsa_circ_165948,RMVar_hsa_circ_313160 25741 RMVar_ID_25741 Human_SNP_ID_550892889 A-to-I Human chr14 + 35058839 35058839 35058839 TTGAGGCTGCAGTGAACTGGGATCTCACCACTACATTCCAGTCTAGGTGACAGAGTAAGACCTTG TTGAGGCTGCAGTGAACTGGGATCTCACCACTGCATTCCAGTCTAGGTGACAGAGTAAGACCTTG A G FAM177A1 Ensembl:ENSG00000151327 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs775145073 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17562462 RMVar_hsa_circ_310328,RMVar_hsa_circ_347276,RMVar_hsa_circ_165952 25742 RMVar_ID_25742 Human_SNP_ID_550899258 A-to-I Human chr14 + 35084034 35084034 35084034 GGGCTTAAGCAGTCCTTCCCTGTCAGCCTCCTAAGGATCTGGGACTACAGGCTCACACCACCATG GGGCTTAAGCAGTCCTTCCCTGTCAGCCTCCTTAGGATCTGGGACTACAGGCTCACACCACCATG A T FAM177A1 Ensembl:ENSG00000151327 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167236041 Functional Loss SNV dbSNP153 33..33 33 - - - 25743 RMVar_ID_25743 Human_SNP_ID_550901790 A-to-I Human chr14 - 35092670 35092670 35092670 CTGAGGTTGGGAGTTTTGAGACCAGCCTGACCAACTTGGAGAAACCGCTTCTCTACTAAAAATAC CTGAGGTTGGGAGTTTTGAGACCAGCCTGACCGACTTGGAGAAACCGCTTCTCTACTAAAAATAC T C PPP2R3C Ensembl:ENSG00000092020 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1292982128 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28180,RMVar_hsa_circ_99186,RMVar_hsa_circ_165954,RMVar_hsa_circ_165957,RMVar_hsa_circ_36685,RMVar_hsa_circ_306869,RMVar_hsa_circ_165956,RMVar_hsa_circ_299361,RMVar_hsa_circ_165958,RMVar_hsa_circ_330258,RMVar_hsa_circ_339978,RMVar_hsa_circ_354072,RMVar_hsa_circ_338236,RMVar_hsa_circ_323876,RMVar_hsa_circ_165959,RMVar_hsa_circ_165961,RMVar_hsa_circ_165962,RMVar_hsa_circ_165963,RMVar_hsa_circ_165960 25744 RMVar_ID_25744 Human_SNP_ID_550902220 A-to-I Human chr14 - 35094299 35094299 35094299 GGGCATGGATGGAATGTGCCTGTAGTATAGCTACTCGGGAGGCTGAGGCAGGAGGATTGCTTGAC GGGCATGGATGGAATGTGCCTGTAGTATAGCTCCTCGGGAGGCTGAGGCAGGAGGATTGCTTGAC T G PPP2R3C Ensembl:ENSG00000092020 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1301624166 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28180,RMVar_hsa_circ_99186,RMVar_hsa_circ_165954,RMVar_hsa_circ_165957,RMVar_hsa_circ_36685,RMVar_hsa_circ_306869,RMVar_hsa_circ_165956,RMVar_hsa_circ_299361,RMVar_hsa_circ_165958,RMVar_hsa_circ_330258,RMVar_hsa_circ_339978,RMVar_hsa_circ_354072,RMVar_hsa_circ_338236,RMVar_hsa_circ_323876,RMVar_hsa_circ_165959,RMVar_hsa_circ_165961,RMVar_hsa_circ_165962,RMVar_hsa_circ_165963,RMVar_hsa_circ_165960 25745 RMVar_ID_25745 Human_SNP_ID_550902370 A-to-I Human chr14 - 35094896 35094896 35094896 AGGCTAGAGTGCAGTGGTGTGATCTCCGCTCAATGCAACCTCCACTTCCTAGGTTCAAGTGATTC AGGCTAGAGTGCAGTGGTGTGATCTCCGCTCAGTGCAACCTCCACTTCCTAGGTTCAAGTGATTC T C PPP2R3C Ensembl:ENSG00000092020 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs749861201 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28180,RMVar_hsa_circ_99186,RMVar_hsa_circ_165954,RMVar_hsa_circ_165957,RMVar_hsa_circ_36685,RMVar_hsa_circ_306869,RMVar_hsa_circ_165956,RMVar_hsa_circ_299361,RMVar_hsa_circ_165958,RMVar_hsa_circ_330258,RMVar_hsa_circ_339978,RMVar_hsa_circ_354072,RMVar_hsa_circ_338236,RMVar_hsa_circ_323876,RMVar_hsa_circ_165959,RMVar_hsa_circ_165961,RMVar_hsa_circ_165962,RMVar_hsa_circ_165963,RMVar_hsa_circ_165960 25746 RMVar_ID_25746 Human_SNP_ID_550903053 A-to-I Human chr14 - 35097179 35097179 35097179 TGGAGTTTTGCTCTTGTTCCCTAGGCTGTAGTACAATGGCTTGATCTCAGCTCACTGCAACCTCT TGGAGTTTTGCTCTTGTTCCCTAGGCTGTAGTGCAATGGCTTGATCTCAGCTCACTGCAACCTCT T C PPP2R3C Ensembl:ENSG00000092020 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs553579608 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28180,RMVar_hsa_circ_99186,RMVar_hsa_circ_165954,RMVar_hsa_circ_165957,RMVar_hsa_circ_306869,RMVar_hsa_circ_165956,RMVar_hsa_circ_299361,RMVar_hsa_circ_165958,RMVar_hsa_circ_330258,RMVar_hsa_circ_339978,RMVar_hsa_circ_323876,RMVar_hsa_circ_38570,RMVar_hsa_circ_165961,RMVar_hsa_circ_165962,RMVar_hsa_circ_165963,RMVar_hsa_circ_316521,RMVar_hsa_circ_368616,RMVar_hsa_circ_274248,RMVar_hsa_circ_40987,RMVar_hsa_circ_165964,RMVar_hsa_circ_165965,RMVar_hsa_circ_286437,RMVar_hsa_circ_361349,RMVar_hsa_circ_285986,RMVar_hsa_circ_165968,RMVar_hsa_circ_165969 25747 RMVar_ID_25747 Human_SNP_ID_550908462 A-to-I Human chr14 - 35119541 35119541 35119541 GGCCAGGAGTTTGAGACCAGCCTGGGCAACATAGTGAAACACCGTTTCTACAAAAATAGAAAGTA GGCCAGGAGTTTGAGACCAGCCTGGGCAACATCGTGAAACACCGTTTCTACAAAAATAGAAAGTA T G PPP2R3C Ensembl:ENSG00000092020 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1408239522 Functional Loss SNV dbSNP153 33..33 33 - - - 25748 RMVar_ID_25748 Human_SNP_ID_550910211 A-to-I Human chr14 + 35124916 35124916 35124916 TTGAGACGGAGTTTTGCTCTTGTTGCCAGGCTAGAGTGCAATGGCATGATCTCGGCTCATTGTAA TTGAGACGGAGTTTTGCTCTTGTTGCCAGGCTGGAGTGCAATGGCATGATCTCGGCTCATTGTAA A G AL121594.1,PRORP Ensembl:ENSG00000258790,Ensembl:ENSG00000100890 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs989274385 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49804,RMVar_hsa_circ_354649,RMVar_hsa_circ_359030,RMVar_hsa_circ_53435 25749 RMVar_ID_25749 Human_SNP_ID_550945994 A-to-I Human chr14 + 35273951 35273951 35273951 GCAGAATCAATCCATCTGTCCCTGAGATACTCATGTTGTTTCAAATGCCTCCTCCCATTTCTGGC GCAGAATCAATCCATCTGTCCCTGAGATACTCGTGTTGTTTCAAATGCCTCCTCCCATTTCTGGC A G AL121594.1,PRORP Ensembl:ENSG00000258790,Ensembl:ENSG00000100890 Protein coding,Protein coding 3'UTR,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs765912617 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5112365,Human_RBP_ID_12322807,Human_RBP_ID_18273101 25750 RMVar_ID_25750 Human_SNP_ID_550946120 A-to-I Human chr14 + 35274483 35274483 35274483 CAGCCTAGGCAACATAGTAAGATCTCATTTCTACAAAAAATTTAAAAATTAGCCAGGCATGGTAG CAGCCTAGGCAACATAGTAAGATCTCATTTCTTCAAAAAATTTAAAAATTAGCCAGGCATGGTAG A T AL121594.1,PRORP Ensembl:ENSG00000258790,Ensembl:ENSG00000100890 Protein coding,Protein coding intron,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1261150977 Functional Loss SNV dbSNP153 33..33 33 - - - 25751 RMVar_ID_25751 Human_SNP_ID_550946453 A-to-I Human chr14 + 35276047 35276047 35276047 GATGGGGGAGGAGTCAGGGCATGGTGGCCCACACCTACAGTTCCAGCACTTTGGGAGGCCAAATG GATGGGGGAGGAGTCAGGGCATGGTGGCCCACTCCTACAGTTCCAGCACTTTGGGAGGCCAAATG A T AL121594.1,PRORP Ensembl:ENSG00000258790,Ensembl:ENSG00000100890 Protein coding,Protein coding intron,3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs936336567 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17562478,Human_RBP_ID_17847835 25752 RMVar_ID_25752 Human_SNP_ID_550946456 A-to-I Human chr14 + 35276053 35276053 35276053 GGAGGAGTCAGGGCATGGTGGCCCACACCTACAGTTCCAGCACTTTGGGAGGCCAAATGGGAGAA GGAGGAGTCAGGGCATGGTGGCCCACACCTACGGTTCCAGCACTTTGGGAGGCCAAATGGGAGAA A G AL121594.1,PRORP Ensembl:ENSG00000258790,Ensembl:ENSG00000100890 Protein coding,Protein coding intron,3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1214630933 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17562478,Human_RBP_ID_17847835 25753 RMVar_ID_25753 Human_SNP_ID_550946467 A-to-I Human chr14 + 35276117 35276117 35276117 ATTGCTTGAAGCCAGGAGTTGGAGACCAGCCTAGGCAACACAGGGAGACCCGTGTCGACAAAAAA ATTGCTTGAAGCCAGGAGTTGGAGACCAGCCTGGGCAACACAGGGAGACCCGTGTCGACAAAAAA A G AL121594.1,PRORP Ensembl:ENSG00000258790,Ensembl:ENSG00000100890 Protein coding,Protein coding intron,3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs906032999 Functional Loss SNV dbSNP153 33..33 33 - - - 25754 RMVar_ID_25754 Human_SNP_ID_550946483 A-to-I Human chr14 + 35276252 35276252 35276252 TCACTTGAGCCCCAGAGGTCAAGGCTACAGTGAGCTATGATCATGCTACTACACTCCAGCCTAGG TCACTTGAGCCCCAGAGGTCAAGGCTACAGTGGGCTATGATCATGCTACTACACTCCAGCCTAGG A G AL121594.1,PRORP Ensembl:ENSG00000258790,Ensembl:ENSG00000100890 Protein coding,Protein coding intron,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs962420501 Functional Loss SNV dbSNP153 33..33 33 - - - 25755 RMVar_ID_25755 Human_SNP_ID_550946484 A-to-I Human chr14 + 35276256 35276256 35276256 TTGAGCCCCAGAGGTCAAGGCTACAGTGAGCTATGATCATGCTACTACACTCCAGCCTAGGTGAC TTGAGCCCCAGAGGTCAAGGCTACAGTGAGCTGTGATCATGCTACTACACTCCAGCCTAGGTGAC A G AL121594.1,PRORP Ensembl:ENSG00000258790,Ensembl:ENSG00000100890 Protein coding,Protein coding intron,3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229,31158229 RNA-Seq:(High) rs561882831 Functional Loss SNV dbSNP153 33..33 33 - - - 25756 RMVar_ID_25756 Human_SNP_ID_550946661 A-to-I Human chr14 + 35277081 35277081 35277081 GTCTTGATCTTTTTTCATCTAGGCTGGAGTGCAATGGTTTGATCTCAGTTCACTGCAACCTCTGC GTCTTGATCTTTTTTCATCTAGGCTGGAGTGCCATGGTTTGATCTCAGTTCACTGCAACCTCTGC A C AL121594.1,PRORP Ensembl:ENSG00000258790,Ensembl:ENSG00000100890 Protein coding,Protein coding intron,3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs942215111 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18273106 25757 RMVar_ID_25757 Human_SNP_ID_550946662 A-to-I Human chr14 + 35277081 35277081 35277081 GTCTTGATCTTTTTTCATCTAGGCTGGAGTGCAATGGTTTGATCTCAGTTCACTGCAACCTCTGC GTCTTGATCTTTTTTCATCTAGGCTGGAGTGCGATGGTTTGATCTCAGTTCACTGCAACCTCTGC A G AL121594.1,PRORP Ensembl:ENSG00000258790,Ensembl:ENSG00000100890 Protein coding,Protein coding intron,3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs942215111 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18273106 25758 RMVar_ID_25758 Human_SNP_ID_550946691 A-to-I Human chr14 + 35277209 35277209 35277209 CATGACGCCTGGCTAATTTTTGCATTTTTAGTAGAGACGGGTTTTCACCATGTTGCCCCGGTTGC CATGACGCCTGGCTAATTTTTGCATTTTTAGTGGAGACGGGTTTTCACCATGTTGCCCCGGTTGC A G AL121594.1,PRORP Ensembl:ENSG00000258790,Ensembl:ENSG00000100890 Protein coding,Protein coding intron,3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1335519158 Functional Loss SNV dbSNP153 33..33 33 - - - 25759 RMVar_ID_25759 Human_SNP_ID_550946698 A-to-I Human chr14 + 35277226 35277226 35277226 TTTTGCATTTTTAGTAGAGACGGGTTTTCACCATGTTGCCCCGGTTGCTCTCAAACTCCTGACCT TTTTGCATTTTTAGTAGAGACGGGTTTTCACCGTGTTGCCCCGGTTGCTCTCAAACTCCTGACCT A G AL121594.1,PRORP Ensembl:ENSG00000258790,Ensembl:ENSG00000100890 Protein coding,Protein coding intron,3'UTR GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1408387655 Functional Loss SNV dbSNP153 33..33 33 - - - 25760 RMVar_ID_25760 Human_SNP_ID_550946934 A-to-I Human chr14 + 35278244 35278244 35278244 TTTCCTGGCCGGGTGCAGTGACTCATGTCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGAGG TTTCCTGGCCGGGTGCAGTGACTCATGTCTGTTATCCCAGCACTTTGGGAGGCCGAGGCGGGAGG A T AL121594.1 Ensembl:ENSG00000258790 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs974983626 Functional Loss SNV dbSNP153 33..33 33 - - - 25761 RMVar_ID_25761 Human_SNP_ID_550948614 A-to-I Human chr14 + 35285289 35285289 35285289 GATCGCCTGGGAGGCAGAGGTTGCAGTGAGCCAAGATCGTGCCACTGCACTCTAGCCAGAGTGAC GATCGCCTGGGAGGCAGAGGTTGCAGTGAGCCGAGATCGTGCCACTGCACTCTAGCCAGAGTGAC A G AL121594.1,PSMA6 Ensembl:ENSG00000258790,Ensembl:ENSG00000100902 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1244766893 Functional Loss SNV dbSNP153 33..33 33 - - - 25762 RMVar_ID_25762 Human_SNP_ID_550949604 A-to-I Human chr14 + 35289686 35289686 35289686 ATAACAGAAAGAAAAAAGATACTCAGGAGGCTAAGGCCAAAGGATCCCTTGAGGCCAGGAGTTTG ATAACAGAAAGAAAAAAGATACTCAGGAGGCTGAGGCCAAAGGATCCCTTGAGGCCAGGAGTTTG A G AL121594.1,PSMA6 Ensembl:ENSG00000258790,Ensembl:ENSG00000100902 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1206079031 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17562482 25763 RMVar_ID_25763 Human_SNP_ID_550951176 A-to-I Human chr14 + 35295230 35295230 35295230 TTGTGCTGGCGTGCCTGTAGTCCTACCTCCTCAGGAAGCTGAGGCACAAGAATCGCTTGAACCTA TTGTGCTGGCGTGCCTGTAGTCCTACCTCCTCGGGAAGCTGAGGCACAAGAATCGCTTGAACCTA A G AL121594.1,PSMA6 Ensembl:ENSG00000258790,Ensembl:ENSG00000100902 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs559783564 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90474,RMVar_hsa_circ_165976 25764 RMVar_ID_25764 Human_SNP_ID_550951185 A-to-I Human chr14 + 35295262 35295262 35295262 AGGAAGCTGAGGCACAAGAATCGCTTGAACCTAGGAGGCAGAGGTTGCAGTGAGCCAAGACCGTG AGGAAGCTGAGGCACAAGAATCGCTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCCAAGACCGTG A G AL121594.1,PSMA6 Ensembl:ENSG00000258790,Ensembl:ENSG00000100902 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1346714428 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90474,RMVar_hsa_circ_165976 25765 RMVar_ID_25765 Human_SNP_ID_550953401 A-to-I Human chr14 + 35303992 35303992 35303992 TAAGCTAGAGATAATTTCTTTCTTTTTTTTTTAGACGGAGTCTCGCTCTGTAGCCCAGGCTGGAG TAAGCTAGAGATAATTTCTTTCTTTTTTTTTTTGACGGAGTCTCGCTCTGTAGCCCAGGCTGGAG A T AL121594.1,PSMA6 Ensembl:ENSG00000258790,Ensembl:ENSG00000100902 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335276195 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6343762 RMVar_hsa_circ_90474,RMVar_hsa_circ_165976 25766 RMVar_ID_25766 Human_SNP_ID_550954283 A-to-I Human chr14 + 35307532 35307532 35307532 AAGGCAGGTGGATCACCTGAGGTCAGGAGTTCAAGACTAGCCTGGCCAACACAGCGAAACCCCGT AAGGCAGGTGGATCACCTGAGGTCAGGAGTTCGAGACTAGCCTGGCCAACACAGCGAAACCCCGT A G AL121594.1,PSMA6 Ensembl:ENSG00000258790,Ensembl:ENSG00000100902 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1422219827 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90474,RMVar_hsa_circ_165976 25767 RMVar_ID_25767 Human_SNP_ID_550954312 A-to-I Human chr14 + 35307619 35307619 35307619 AGCCAGATGTGGTGGCACGCGCCTATAATCCCAGCTACTTAGGAGGCTGAGGCAGGAGACTAGCG AGCCAGATGTGGTGGCACGCGCCTATAATCCCGGCTACTTAGGAGGCTGAGGCAGGAGACTAGCG A G AL121594.1,PSMA6 Ensembl:ENSG00000258790,Ensembl:ENSG00000100902 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs552310944 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90474,RMVar_hsa_circ_165976 25768 RMVar_ID_25768 Human_SNP_ID_550954313 A-to-I Human chr14 + 35307623 35307623 35307623 AGATGTGGTGGCACGCGCCTATAATCCCAGCTACTTAGGAGGCTGAGGCAGGAGACTAGCGTTAA AGATGTGGTGGCACGCGCCTATAATCCCAGCTGCTTAGGAGGCTGAGGCAGGAGACTAGCGTTAA A G AL121594.1,PSMA6 Ensembl:ENSG00000258790,Ensembl:ENSG00000100902 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1263743086 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90474,RMVar_hsa_circ_165976 25769 RMVar_ID_25769 Human_SNP_ID_550957149 A-to-I Human chr14 + 35318586 35318586 35318586 AGGTTCATTCATGTTATAAATAACAGGATTTCATTCTTTTTAATAGCTGAATAGTGTTCCTTTGT AGGTTCATTCATGTTATAAATAACAGGATTTCGTTCTTTTTAATAGCTGAATAGTGTTCCTTTGT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs765689364 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_445233,Human_RBP_ID_2412364 25770 RMVar_ID_25770 Human_SNP_ID_551012860 A-to-I Human chr14 - 35543783 35543783 35543783 CAAAAATTAGCTGGGCATGATGGCATGCGCCTATAATCCCAGCTACTCAGGAGGCTGAGGCAGGA CAAAAATTAGCTGGGCATGATGGCATGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGA T C RALGAPA1 Ensembl:ENSG00000174373 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1041332382 Functional Loss SNV dbSNP153 33..33 33 - - - 25771 RMVar_ID_25771 Human_SNP_ID_551013088 A-to-I Human chr14 - 35544960 35544960 35544960 TCACTGCAACCTCCACCTCCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCTCAAGTAGCTGGGA TCACTGCAACCTCCACCTCCCGGGTTCAAGCAGTTCTCCTGCCTCAGCCTCTCAAGTAGCTGGGA T C RALGAPA1 Ensembl:ENSG00000174373 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs753764760 Functional Loss SNV dbSNP153 33..33 33 - - - 25772 RMVar_ID_25772 Human_SNP_ID_551013089 A-to-I Human chr14 - 35544961 35544961 35544961 CTCACTGCAACCTCCACCTCCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCTCAAGTAGCTGGG CTCACTGCAACCTCCACCTCCCGGGTTCAAGCCATTCTCCTGCCTCAGCCTCTCAAGTAGCTGGG T G RALGAPA1 Ensembl:ENSG00000174373 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1347544274 Functional Loss SNV dbSNP153 33..33 33 - - - 25773 RMVar_ID_25773 Human_SNP_ID_551013093 A-to-I Human chr14 - 35544978 35544978 35544978 CAGTGGCGCAATCTTGGCTCACTGCAACCTCCACCTCCCGGGTTCAAGCAATTCTCCTGCCTCAG CAGTGGCGCAATCTTGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGCAATTCTCCTGCCTCAG T C RALGAPA1 Ensembl:ENSG00000174373 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1046268337 Functional Loss SNV dbSNP153 33..33 33 - - - 25774 RMVar_ID_25774 Human_SNP_ID_551063265 A-to-I Human chr14 - 35768070 35768068 35768071 AGACACAATCTCTAAAACATGAAAATAAGGACAGATGTGGTGGCTCATGCCTATAATCCCAGCAC AGACACAATCTCTAAAACATGAAAATAAGGA___ATGTGGTGGCTCATGCCTATAATCCCAGCAC TCTG T RALGAPA1 Ensembl:ENSG00000174373 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs774040109 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_78773,RMVar_hsa_circ_165985,RMVar_hsa_circ_109757,RMVar_hsa_circ_165996,RMVar_hsa_circ_166003,RMVar_hsa_circ_91079,RMVar_hsa_circ_112979,RMVar_hsa_circ_166005,RMVar_hsa_circ_71634,RMVar_hsa_circ_9586,RMVar_hsa_circ_345107,RMVar_hsa_circ_73460,RMVar_hsa_circ_67115,RMVar_hsa_circ_309206,RMVar_hsa_circ_353583,RMVar_hsa_circ_335377,RMVar_hsa_circ_330398,RMVar_hsa_circ_335659,RMVar_hsa_circ_339817 25775 RMVar_ID_25775 Human_SNP_ID_551068914 A-to-I Human chr14 - 35792423 35792423 35792423 AGCTGGCATGGTGGTTCATGCCTATAATCCCAACACTTTGAGAGGCTGAGGCGGGTGGATCGCTT AGCTGGCATGGTGGTTCATGCCTATAATCCCAGCACTTTGAGAGGCTGAGGCGGGTGGATCGCTT T C RALGAPA1 Ensembl:ENSG00000174373 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs987610363 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78773,RMVar_hsa_circ_165985 25776 RMVar_ID_25776 Human_SNP_ID_551069769 A-to-I Human chr14 - 35795772 35795772 35795772 TGGGGTTTTGCTATGTTGCCCAGGCTGGCCTCAAGCTCCTGGTCTCAAGTGATCTGCCCACCTTG TGGGGTTTTGCTATGTTGCCCAGGCTGGCCTCGAGCTCCTGGTCTCAAGTGATCTGCCCACCTTG T C RALGAPA1 Ensembl:ENSG00000174373 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1444679353 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12460345 RMVar_hsa_circ_78773,RMVar_hsa_circ_165985 25777 RMVar_ID_25777 Human_SNP_ID_551082197 A-to-I Human chr14 + 35845825 35845825 35845825 GGAGTGCAGTGGCTGTTCACCAGCGTGATCATAGTGCACTGCAGCCTTGAATTCCTGGCCTCAAG GGAGTGCAGTGGCTGTTCACCAGCGTGATCATGGTGCACTGCAGCCTTGAATTCCTGGCCTCAAG A G BRMS1L Ensembl:ENSG00000100916 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1452404106 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47760 25778 RMVar_ID_25778 Human_SNP_ID_551088640 A-to-I Human chr14 + 35873657 35873638 35873657 AAAATTACCTGGGTGTGGTGGCGCGCACCTGTAGTTCCAGCTACTTGGGAAGCTGAGGCAGGAGA AAAATTACCTGGGT___________________GTTCCAGCTACTTGGGAAGCTGAGGCAGGAGA TGTGGTGGCGCGCACCTGTA T BRMS1L Ensembl:ENSG00000100916 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1566435342 Functional Loss DEL dbSNP153 15..33 33 - - - 25779 RMVar_ID_25779 Human_SNP_ID_551413028 A-to-I Human chr14 + 37219570 37219570 37219570 TTTAATGTTTTGTAGGAACGAGGTCTCACTATATTGCCCAGACTGGTCTCGAACTCCTGGGCTCA TTTAATGTTTTGTAGGAACGAGGTCTCACTATGTTGCCCAGACTGGTCTCGAACTCCTGGGCTCA A G MIPOL1 Ensembl:ENSG00000151338 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1010760612 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1508286,Human_Splice_Rec_1508386 RMVar_hsa_circ_1609,RMVar_hsa_circ_62873,RMVar_hsa_circ_334069,RMVar_hsa_circ_62961,RMVar_hsa_circ_166023,RMVar_hsa_circ_24773,RMVar_hsa_circ_166024,RMVar_hsa_circ_88024,RMVar_hsa_circ_166026,RMVar_hsa_circ_166027,RMVar_hsa_circ_166025 25780 RMVar_ID_25780 Human_SNP_ID_551485094 A-to-I Human chr14 + 37509895 37509895 37509895 ATGTAGGCATTTTTTAAATTAAGAAACTGTAGAAATGCTCTGTTCCTCTTCCCAGCACCCACAGT ATGTAGGCATTTTTTAAATTAAGAAACTGTAGCAATGCTCTGTTCCTCTTCCCAGCACCCACAGT A C MIPOL1 Ensembl:ENSG00000151338 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1477268628 Functional Loss SNV dbSNP153 33..33 33 - - - 25781 RMVar_ID_25781 Human_SNP_ID_551499518 A-to-I Human chr14 + 37571308 37571308 37571308 GTGATCATCCTACCTCTGGCTCCTGAGTAGCTAGGACTACAGGTGTGCACCAGCTTCCTGGCTAA GTGATCATCCTACCTCTGGCTCCTGAGTAGCTCGGACTACAGGTGTGCACCAGCTTCCTGGCTAA A C AL121790.1 Ensembl:ENSG00000258414 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1330530210 Functional Loss SNV dbSNP153 33..33 33 - - - 25782 RMVar_ID_25782 Human_SNP_ID_551864059 A-to-I Human chr14 - 39063832 39063832 39063832 GCCAGCATGCCTGGCTGATTTTTTGTGTTTTTAGTAGAGATGGGGTTTCACCGTGTTAGCCAGGA GCCAGCATGCCTGGCTGATTTTTTGTGTTTTTTGTAGAGATGGGGTTTCACCGTGTTAGCCAGGA T A SEC23A Ensembl:ENSG00000100934 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054845846 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1390,RMVar_hsa_circ_63192,RMVar_hsa_circ_41647,RMVar_hsa_circ_123746,RMVar_hsa_circ_166065,RMVar_hsa_circ_99660,RMVar_hsa_circ_166067,RMVar_hsa_circ_73967,RMVar_hsa_circ_166066,RMVar_hsa_circ_364893,RMVar_hsa_circ_366537,RMVar_hsa_circ_361361,RMVar_hsa_circ_301486,RMVar_hsa_circ_7111,RMVar_hsa_circ_166071,RMVar_hsa_circ_166072,RMVar_hsa_circ_166074,RMVar_hsa_circ_21074,RMVar_hsa_circ_294171,RMVar_hsa_circ_271871,RMVar_hsa_circ_166075,RMVar_hsa_circ_304276,RMVar_hsa_circ_377846,RMVar_hsa_circ_289078,RMVar_hsa_circ_108320,RMVar_hsa_circ_274747,RMVar_hsa_circ_47088,RMVar_hsa_circ_166077,RMVar_hsa_circ_166079,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_292406,RMVar_hsa_circ_294582,RMVar_hsa_circ_166087,RMVar_hsa_circ_166084,RMVar_hsa_circ_166085,RMVar_hsa_circ_166083,RMVar_hsa_circ_166088,RMVar_hsa_circ_36317,RMVar_hsa_circ_354866,RMVar_hsa_circ_357016,RMVar_hsa_circ_117105,RMVar_hsa_circ_166089 25783 RMVar_ID_25783 Human_SNP_ID_551864318 A-to-I Human chr14 - 39064835 39064835 39064835 TGGCTTGCACCTGTAATCCCAGGTACTTGGGAAGCTGAGGCAGGAGGATTGCTTAAGCCCAGGAG TGGCTTGCACCTGTAATCCCAGGTACTTGGGACGCTGAGGCAGGAGGATTGCTTAAGCCCAGGAG T G SEC23A Ensembl:ENSG00000100934 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs923632128 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1390,RMVar_hsa_circ_63192,RMVar_hsa_circ_41647,RMVar_hsa_circ_123746,RMVar_hsa_circ_166065,RMVar_hsa_circ_99660,RMVar_hsa_circ_166067,RMVar_hsa_circ_73967,RMVar_hsa_circ_166066,RMVar_hsa_circ_364893,RMVar_hsa_circ_366537,RMVar_hsa_circ_361361,RMVar_hsa_circ_301486,RMVar_hsa_circ_7111,RMVar_hsa_circ_166071,RMVar_hsa_circ_166072,RMVar_hsa_circ_166074,RMVar_hsa_circ_21074,RMVar_hsa_circ_294171,RMVar_hsa_circ_271871,RMVar_hsa_circ_166075,RMVar_hsa_circ_304276,RMVar_hsa_circ_377846,RMVar_hsa_circ_289078,RMVar_hsa_circ_108320,RMVar_hsa_circ_274747,RMVar_hsa_circ_47088,RMVar_hsa_circ_166077,RMVar_hsa_circ_166079,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_292406,RMVar_hsa_circ_294582,RMVar_hsa_circ_166087,RMVar_hsa_circ_166084,RMVar_hsa_circ_166085,RMVar_hsa_circ_166083,RMVar_hsa_circ_166088,RMVar_hsa_circ_36317,RMVar_hsa_circ_354866,RMVar_hsa_circ_357016,RMVar_hsa_circ_117105,RMVar_hsa_circ_166089 25784 RMVar_ID_25784 Human_SNP_ID_551871694 A-to-I Human chr14 - 39093649 39093649 39093649 TCAGATGATCCTCTCACCTAAGCCTCCTAAGTAACTGGGAGTGCAGGCATGTGCCACCACGCCTG TCAGATGATCCTCTCACCTAAGCCTCCTAAGTGACTGGGAGTGCAGGCATGTGCCACCACGCCTG T C SEC23A Ensembl:ENSG00000100934 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1311409265 Functional Loss SNV dbSNP153 33..33 33 - - - 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_166100,RMVar_hsa_circ_374003,RMVar_hsa_circ_166101,RMVar_hsa_circ_281670 25785 RMVar_ID_25785 Human_SNP_ID_551878340 A-to-I Human chr14 + 39116774 39116773 39116775 TTTGATGGATTGATTGATTGATTGATTGAGACAGGGTCTCGCTTTGTTGCACAGGCCAGAGTACA TTTGATGGATTGATTGATTGATTGATTGAGAC__GGTCTCGCTTTGTTGCACAGGCCAGAGTACA CAG C GEMIN2 Ensembl:ENSG00000092208 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1261037267 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_7435,RMVar_hsa_circ_55847,RMVar_hsa_circ_373520,RMVar_hsa_circ_10770,RMVar_hsa_circ_166104 25786 RMVar_ID_25786 Human_SNP_ID_551880758 A-to-I Human chr14 + 39126369 39126369 39126369 CCTGGCTAATTTTGTTTATTTTTGGTAGAGACAAGGTCTCACTGTGTTGTCCAGGCTGGTCTGGA CCTGGCTAATTTTGTTTATTTTTGGTAGAGACCAGGTCTCACTGTGTTGTCCAGGCTGGTCTGGA A C GEMIN2 Ensembl:ENSG00000092208 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1249921354 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_373520,RMVar_hsa_circ_302105,RMVar_hsa_circ_344522,RMVar_hsa_circ_166104,RMVar_hsa_circ_354848,RMVar_hsa_circ_166107,RMVar_hsa_circ_166108,RMVar_hsa_circ_376376,RMVar_hsa_circ_363116 25787 RMVar_ID_25787 Human_SNP_ID_551881741 A-to-I Human chr14 + 39129674 39129674 39129674 ACCTCAGGTGATCTGCCCGCCTCCACCTCTCAAAGTGTTGGAATTACAGGCGTGAGCCACTGCAC ACCTCAGGTGATCTGCCCGCCTCCACCTCTCACAGTGTTGGAATTACAGGCGTGAGCCACTGCAC A C GEMIN2 Ensembl:ENSG00000092208 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs897239833 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_373520,RMVar_hsa_circ_302105,RMVar_hsa_circ_344522,RMVar_hsa_circ_166104,RMVar_hsa_circ_166107,RMVar_hsa_circ_5800,RMVar_hsa_circ_166108,RMVar_hsa_circ_376376,RMVar_hsa_circ_351189,RMVar_hsa_circ_363116 25788 RMVar_ID_25788 Human_SNP_ID_551882147 A-to-I Human chr14 + 39131190 39131190 39131190 GTGGTGGTACATGCCTGTAATTCCAGGTACTCAGGATGCTGAGACAGGAGAATTGCTTGAACCCG GTGGTGGTACATGCCTGTAATTCCAGGTACTCGGGATGCTGAGACAGGAGAATTGCTTGAACCCG A G GEMIN2 Ensembl:ENSG00000092208 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs372967246 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_373520,RMVar_hsa_circ_302105,RMVar_hsa_circ_344522,RMVar_hsa_circ_166104,RMVar_hsa_circ_166107,RMVar_hsa_circ_5800,RMVar_hsa_circ_166108,RMVar_hsa_circ_376376,RMVar_hsa_circ_351189,RMVar_hsa_circ_363116 25789 RMVar_ID_25789 Human_SNP_ID_551885474 A-to-I Human chr14 - 39143789 39143789 39143789 CTCCGGCCTCAGCCTTCTGAGTAGCTGGGATTACAGGTGCCTACCACCACACCTGGCTAATTGTT CTCCGGCCTCAGCCTTCTGAGTAGCTGGGATTGCAGGTGCCTACCACCACACCTGGCTAATTGTT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1012430802 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_166109 25790 RMVar_ID_25790 Human_SNP_ID_551886411 A-to-I Human chr14 - 39146963 39146963 39146963 CTGGCTCACACCTGTAATCCCAACACTTTGGAAGGCCAGAGTGGGCGGATGACCCGAGATCAGGA CTGGCTCACACCTGTAATCCCAACACTTTGGAGGGCCAGAGTGGGCGGATGACCCGAGATCAGGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1180594589 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_166109 25791 RMVar_ID_25791 Human_SNP_ID_551887314 A-to-I Human chr14 - 39150810 39150810 39150810 TTGACTGGCCGGGTGTGGTGCCTCACACCTGTAAGCTCAGCACTTTGGGAGGCCGAGGTGGGCGT TTGACTGGCCGGGTGTGGTGCCTCACACCTGTTAGCTCAGCACTTTGGGAGGCCGAGGTGGGCGT T A TRAPPC6B Ensembl:ENSG00000182400 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1160422472 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114634,RMVar_hsa_circ_166109,RMVar_hsa_circ_166111,RMVar_hsa_circ_166110 25792 RMVar_ID_25792 Human_SNP_ID_551888095 A-to-I Human chr14 - 39153514 39153514 39153514 GTGATCCTCCCACTTCAGTCACCCAAGGAGGTAGGACTGCAGGTGTGGGCCACCATGCCTGGCTA GTGATCCTCCCACTTCAGTCACCCAAGGAGGTGGGACTGCAGGTGTGGGCCACCATGCCTGGCTA T C TRAPPC6B Ensembl:ENSG00000182400 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1424293431 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6347734,Human_RBP_ID_12329320 RMVar_hsa_circ_166112,RMVar_hsa_circ_114634,RMVar_hsa_circ_166109,RMVar_hsa_circ_166111,RMVar_hsa_circ_166110,RMVar_hsa_circ_166114,RMVar_hsa_circ_320625,RMVar_hsa_circ_321686,RMVar_hsa_circ_298907,RMVar_hsa_circ_166113 25793 RMVar_ID_25793 Human_SNP_ID_551890999 A-to-I Human chr14 - 39164274 39164274 39164274 GTCGGTAAAGCTGGTCTCGAACTCCTGACCTCAGGTAATCCGCCTGCCTCGGCCTCCCAAAATGC GTCGGTAAAGCTGGTCTCGAACTCCTGACCTCGGGTAATCCGCCTGCCTCGGCCTCCCAAAATGC T C TRAPPC6B Ensembl:ENSG00000182400 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1193770724 Functional Loss SNV dbSNP153 33..33 33 - - - 25794 RMVar_ID_25794 Human_SNP_ID_551891142 A-to-I Human chr14 - 39164823 39164823 39164823 TTGTTTGTTGGTTTGTTTTGAGACAGGATCTCACTCTGTTGCCCGGTCTAGAGTGCAGTGGCTAG TTGTTTGTTGGTTTGTTTTGAGACAGGATCTCGCTCTGTTGCCCGGTCTAGAGTGCAGTGGCTAG T C TRAPPC6B Ensembl:ENSG00000182400 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs887098418 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8403763,Human_RBP_ID_12329510,Human_RBP_ID_22473170 25795 RMVar_ID_25795 Human_SNP_ID_551891146 A-to-I Human chr14 - 39164831 39164831 39164831 TTTTTTGTTTGTTTGTTGGTTTGTTTTGAGACAGGATCTCACTCTGTTGCCCGGTCTAGAGTGCA TTTTTTGTTTGTTTGTTGGTTTGTTTTGAGACGGGATCTCACTCTGTTGCCCGGTCTAGAGTGCA T C TRAPPC6B Ensembl:ENSG00000182400 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs914796468 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8403763,Human_RBP_ID_12329510,Human_RBP_ID_22473170 25796 RMVar_ID_25796 Human_SNP_ID_551892094 A-to-I Human chr14 - 39168164 39168164 39168164 TCTCCCAGGCTGGAGTGCAGTGGTGTGATCTCAGCTCACTGCAGCCTCCGCCTCTTGGGTTCAAG TCTCCCAGGCTGGAGTGCAGTGGTGTGATCTCTGCTCACTGCAGCCTCCGCCTCTTGGGTTCAAG T A TRAPPC6B Ensembl:ENSG00000182400 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs774379644 Functional Loss SNV dbSNP153 33..33 33 - - - 25797 RMVar_ID_25797 Human_SNP_ID_551892095 A-to-I Human chr14 - 39168164 39168164 39168164 TCTCCCAGGCTGGAGTGCAGTGGTGTGATCTCAGCTCACTGCAGCCTCCGCCTCTTGGGTTCAAG TCTCCCAGGCTGGAGTGCAGTGGTGTGATCTCGGCTCACTGCAGCCTCCGCCTCTTGGGTTCAAG T C TRAPPC6B Ensembl:ENSG00000182400 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs774379644 Functional Loss SNV dbSNP153 33..33 33 - - - 25798 RMVar_ID_25798 Human_SNP_ID_551895687 A-to-I Human chr14 + 39178864 39178864 39178864 GGTTCAAGTGATTTCTCCTGCTTCGGCCTCCCAAGTAGCTGGGATTATAGGTGCGTGCAACCACG GGTTCAAGTGATTTCTCCTGCTTCGGCCTCCCGAGTAGCTGGGATTATAGGTGCGTGCAACCACG A G PNN Ensembl:ENSG00000100941 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1353900843 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17562525,Human_RBP_ID_18650399 RMVar_hsa_circ_124902,RMVar_hsa_circ_166121,RMVar_hsa_circ_166120,RMVar_hsa_circ_352048 25799 RMVar_ID_25799 Human_SNP_ID_551900361 A-to-I Human chr14 + 39194348 39194348 39194348 CCAGGAGGTGGAGGTTGCAGTGAGCCAAGATCATGCCACTGCACTCCAGCCTGAGCGACAGAGAC CCAGGAGGTGGAGGTTGCAGTGAGCCAAGATCGTGCCACTGCACTCCAGCCTGAGCGACAGAGAC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350007076 Functional Loss SNV dbSNP153 33..33 33 - - - 25800 RMVar_ID_25800 Human_SNP_ID_551921518 A-to-I Human chr14 + 39274529 39274529 39274529 TGGCTCACTGTAGCCTCCTCCCGGGTTCAGGCAATTCTTGTATCTCAGCCTCCCAAGTAGCTGGG TGGCTCACTGTAGCCTCCTCCCGGGTTCAGGCGATTCTTGTATCTCAGCCTCCCAAGTAGCTGGG A G MIA2 Ensembl:ENSG00000150527 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232359505 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17562529 RMVar_hsa_circ_64128,RMVar_hsa_circ_55578 25801 RMVar_ID_25801 Human_SNP_ID_551921640 A-to-I Human chr14 + 39275019 39275019 39275019 ATTGCTTGAACCCAGGAGACGGAGGTTGCAGTAAGCCTACACGGTGCCGCTGTACTCCAGCCTCG ATTGCTTGAACCCAGGAGACGGAGGTTGCAGTGAGCCTACACGGTGCCGCTGTACTCCAGCCTCG A G MIA2 Ensembl:ENSG00000150527 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs538296826 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64128,RMVar_hsa_circ_55578 25802 RMVar_ID_25802 Human_SNP_ID_551921765 A-to-I Human chr14 + 39275388 39275388 39275388 GTCTCAAACTCCTGGCCTCATGTGATCCGCCTACGTTGGCTTCCCAAAGTGCTGGCATGAGCCAC GTCTCAAACTCCTGGCCTCATGTGATCCGCCTGCGTTGGCTTCCCAAAGTGCTGGCATGAGCCAC A G MIA2 Ensembl:ENSG00000150527 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs892831294 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64128,RMVar_hsa_circ_55578 25803 RMVar_ID_25803 Human_SNP_ID_551922284 A-to-I Human chr14 + 39277415 39277415 39277415 GGACATGAGGACACCCGTCTGTGGTCCTGGCTACTCAGGAGGCTGAGGTGGGAGGATTGCCTGAT GGACATGAGGACACCCGTCTGTGGTCCTGGCTGCTCAGGAGGCTGAGGTGGGAGGATTGCCTGAT A G MIA2 Ensembl:ENSG00000150527 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs948989580 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17562531 RMVar_hsa_circ_4344,RMVar_hsa_circ_285306,RMVar_hsa_circ_298198,RMVar_hsa_circ_55578,RMVar_hsa_circ_357639,RMVar_hsa_circ_357844,RMVar_hsa_circ_351998,RMVar_hsa_circ_287283,RMVar_hsa_circ_287827,RMVar_hsa_circ_286680,RMVar_hsa_circ_60983,RMVar_hsa_circ_279700,RMVar_hsa_circ_284519,RMVar_hsa_circ_58306,RMVar_hsa_circ_60297,RMVar_hsa_circ_43322,RMVar_hsa_circ_166126,RMVar_hsa_circ_166128,RMVar_hsa_circ_166129,RMVar_hsa_circ_166130,RMVar_hsa_circ_166127 25804 RMVar_ID_25804 Human_SNP_ID_551922738 A-to-I Human chr14 + 39278158 39278158 39278158 ACCATGCCTGGCTAATTTTTGTATTTTTTTGTAGAGACGGGTTTCACTGTGTTGCTCAGAACTCC ACCATGCCTGGCTAATTTTTGTATTTTTTTGTGGAGACGGGTTTCACTGTGTTGCTCAGAACTCC A G MIA2 Ensembl:ENSG00000150527 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1241489505 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4344,RMVar_hsa_circ_285306,RMVar_hsa_circ_298198,RMVar_hsa_circ_55578,RMVar_hsa_circ_357639,RMVar_hsa_circ_357844,RMVar_hsa_circ_351998,RMVar_hsa_circ_287283,RMVar_hsa_circ_287827,RMVar_hsa_circ_286680,RMVar_hsa_circ_60983,RMVar_hsa_circ_279700,RMVar_hsa_circ_284519,RMVar_hsa_circ_58306,RMVar_hsa_circ_60297,RMVar_hsa_circ_43322,RMVar_hsa_circ_166126,RMVar_hsa_circ_166128,RMVar_hsa_circ_166129,RMVar_hsa_circ_166130,RMVar_hsa_circ_166127 25805 RMVar_ID_25805 Human_SNP_ID_551936293 A-to-I Human chr14 + 39321791 39321789 39321791 GTAATTTTTTTTTTTTTTTGGAGACTGTTTTCACTCTTGTTGCTCAGGCTGGAATGCAGTGGCGC GTAATTTTTTTTTTTTTTTGGAGACTGTTTT__CTCTTGTTGCTCAGGCTGGAATGCAGTGGCGC TCA T MIA2 Ensembl:ENSG00000150527 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1427885170 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_8403849,Human_RBP_ID_12460364 RMVar_hsa_circ_55578,RMVar_hsa_circ_357844,RMVar_hsa_circ_279700,RMVar_hsa_circ_284519,RMVar_hsa_circ_83225,RMVar_hsa_circ_166126,RMVar_hsa_circ_166127,RMVar_hsa_circ_13978,RMVar_hsa_circ_166132,RMVar_hsa_circ_334404,RMVar_hsa_circ_345510,RMVar_hsa_circ_166134,RMVar_hsa_circ_62818,RMVar_hsa_circ_17846,RMVar_hsa_circ_66339,RMVar_hsa_circ_93576,RMVar_hsa_circ_166135,RMVar_hsa_circ_358623,RMVar_hsa_circ_55553,RMVar_hsa_circ_302859,RMVar_hsa_circ_33419,RMVar_hsa_circ_290726,RMVar_hsa_circ_166136,RMVar_hsa_circ_289144,RMVar_hsa_circ_308040,RMVar_hsa_circ_166137,RMVar_hsa_circ_344812,RMVar_hsa_circ_166138,RMVar_hsa_circ_365935,RMVar_hsa_circ_322673,RMVar_hsa_circ_363396 25806 RMVar_ID_25806 Human_SNP_ID_551936322 A-to-I Human chr14 + 39321854 39321854 39321854 GCGATCTCGGCTCACTGCAACCTCTGCCTCCCAGGTAGCTTGGATTCTCCTGCCTCAGCCTCCTG GCGATCTCGGCTCACTGCAACCTCTGCCTCCCGGGTAGCTTGGATTCTCCTGCCTCAGCCTCCTG A G MIA2 Ensembl:ENSG00000150527 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1003112998 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55578,RMVar_hsa_circ_357844,RMVar_hsa_circ_279700,RMVar_hsa_circ_284519,RMVar_hsa_circ_83225,RMVar_hsa_circ_166126,RMVar_hsa_circ_166127,RMVar_hsa_circ_13978,RMVar_hsa_circ_166132,RMVar_hsa_circ_334404,RMVar_hsa_circ_345510,RMVar_hsa_circ_166134,RMVar_hsa_circ_62818,RMVar_hsa_circ_17846,RMVar_hsa_circ_66339,RMVar_hsa_circ_93576,RMVar_hsa_circ_166135,RMVar_hsa_circ_358623,RMVar_hsa_circ_55553,RMVar_hsa_circ_302859,RMVar_hsa_circ_33419,RMVar_hsa_circ_290726,RMVar_hsa_circ_166136,RMVar_hsa_circ_289144,RMVar_hsa_circ_308040,RMVar_hsa_circ_166137,RMVar_hsa_circ_344812,RMVar_hsa_circ_166138,RMVar_hsa_circ_365935,RMVar_hsa_circ_322673,RMVar_hsa_circ_363396 25807 RMVar_ID_25807 Human_SNP_ID_551936360 A-to-I Human chr14 + 39321986 39321986 39321986 TACAAAAGGTTGTTTTGCCACATTGGCTGGCCAGGCTGGTCTCGAACTCCTGACCTTAGGTGATC TACAAAAGGTTGTTTTGCCACATTGGCTGGCCGGGCTGGTCTCGAACTCCTGACCTTAGGTGATC A G MIA2 Ensembl:ENSG00000150527 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1338544243 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12460366 RMVar_hsa_circ_55578,RMVar_hsa_circ_357844,RMVar_hsa_circ_279700,RMVar_hsa_circ_284519,RMVar_hsa_circ_83225,RMVar_hsa_circ_166126,RMVar_hsa_circ_166127,RMVar_hsa_circ_13978,RMVar_hsa_circ_166132,RMVar_hsa_circ_334404,RMVar_hsa_circ_345510,RMVar_hsa_circ_166134,RMVar_hsa_circ_62818,RMVar_hsa_circ_17846,RMVar_hsa_circ_66339,RMVar_hsa_circ_93576,RMVar_hsa_circ_166135,RMVar_hsa_circ_358623,RMVar_hsa_circ_55553,RMVar_hsa_circ_302859,RMVar_hsa_circ_33419,RMVar_hsa_circ_290726,RMVar_hsa_circ_166136,RMVar_hsa_circ_289144,RMVar_hsa_circ_308040,RMVar_hsa_circ_166137,RMVar_hsa_circ_344812,RMVar_hsa_circ_166138,RMVar_hsa_circ_365935,RMVar_hsa_circ_322673,RMVar_hsa_circ_363396 25808 RMVar_ID_25808 Human_SNP_ID_551936918 A-to-I Human chr14 + 39324005 39324005 39324005 GATCCACCAAAGGAGGATGGAGAGTACCTGTTATTTTTCCTTACTTTTATTATCTTTTTAATTTG GATCCACCAAAGGAGGATGGAGAGTACCTGTTGTTTTTCCTTACTTTTATTATCTTTTTAATTTG A G MIA2 Ensembl:ENSG00000150527 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4899219 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6348196 GWAS_ID_2541,GWAS_ID_2542,GWAS_ID_2543,GWAS_ID_2544,GWAS_ID_2545,GWAS_ID_2546,GWAS_ID_2547,GWAS_ID_2548,GWAS_ID_2549 RMVar_hsa_circ_55578,RMVar_hsa_circ_357844,RMVar_hsa_circ_279700,RMVar_hsa_circ_284519,RMVar_hsa_circ_83225,RMVar_hsa_circ_166126,RMVar_hsa_circ_166127,RMVar_hsa_circ_13978,RMVar_hsa_circ_166132,RMVar_hsa_circ_334404,RMVar_hsa_circ_345510,RMVar_hsa_circ_166134,RMVar_hsa_circ_62818,RMVar_hsa_circ_17846,RMVar_hsa_circ_66339,RMVar_hsa_circ_93576,RMVar_hsa_circ_166135,RMVar_hsa_circ_358623,RMVar_hsa_circ_55553,RMVar_hsa_circ_302859,RMVar_hsa_circ_33419,RMVar_hsa_circ_290726,RMVar_hsa_circ_166136,RMVar_hsa_circ_289144,RMVar_hsa_circ_308040,RMVar_hsa_circ_166137,RMVar_hsa_circ_344812,RMVar_hsa_circ_166138,RMVar_hsa_circ_365935,RMVar_hsa_circ_322673,RMVar_hsa_circ_363396 25809 RMVar_ID_25809 Human_SNP_ID_551937090 A-to-I Human chr14 + 39324668 39324668 39324668 TCACTGTGTTGCCCAGGCTGGAGTGCAGTGGCACGATCTCGGTTCACTGCAACCCCTTCCTCTCA TCACTGTGTTGCCCAGGCTGGAGTGCAGTGGCGCGATCTCGGTTCACTGCAACCCCTTCCTCTCA A G MIA2 Ensembl:ENSG00000150527 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1007417139 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55578,RMVar_hsa_circ_357844,RMVar_hsa_circ_279700,RMVar_hsa_circ_284519,RMVar_hsa_circ_83225,RMVar_hsa_circ_166126,RMVar_hsa_circ_166127,RMVar_hsa_circ_13978,RMVar_hsa_circ_166132,RMVar_hsa_circ_334404,RMVar_hsa_circ_345510,RMVar_hsa_circ_166134,RMVar_hsa_circ_62818,RMVar_hsa_circ_17846,RMVar_hsa_circ_66339,RMVar_hsa_circ_93576,RMVar_hsa_circ_166135,RMVar_hsa_circ_358623,RMVar_hsa_circ_55553,RMVar_hsa_circ_302859,RMVar_hsa_circ_33419,RMVar_hsa_circ_290726,RMVar_hsa_circ_166136,RMVar_hsa_circ_289144,RMVar_hsa_circ_308040,RMVar_hsa_circ_166137,RMVar_hsa_circ_344812,RMVar_hsa_circ_166138,RMVar_hsa_circ_365935,RMVar_hsa_circ_322673,RMVar_hsa_circ_363396 25810 RMVar_ID_25810 Human_SNP_ID_551937109 A-to-I Human chr14 + 39324736 39324736 39324736 TCAAATGATTCTTGTTCCTTAGCTTCCCGAGTAGCTGGGATTACAGGCACGTGCCACTGTACCCA TCAAATGATTCTTGTTCCTTAGCTTCCCGAGTTGCTGGGATTACAGGCACGTGCCACTGTACCCA A T MIA2 Ensembl:ENSG00000150527 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs931283639 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55578,RMVar_hsa_circ_357844,RMVar_hsa_circ_279700,RMVar_hsa_circ_284519,RMVar_hsa_circ_83225,RMVar_hsa_circ_166126,RMVar_hsa_circ_166127,RMVar_hsa_circ_13978,RMVar_hsa_circ_166132,RMVar_hsa_circ_334404,RMVar_hsa_circ_345510,RMVar_hsa_circ_166134,RMVar_hsa_circ_62818,RMVar_hsa_circ_17846,RMVar_hsa_circ_66339,RMVar_hsa_circ_93576,RMVar_hsa_circ_166135,RMVar_hsa_circ_358623,RMVar_hsa_circ_55553,RMVar_hsa_circ_302859,RMVar_hsa_circ_33419,RMVar_hsa_circ_290726,RMVar_hsa_circ_166136,RMVar_hsa_circ_289144,RMVar_hsa_circ_308040,RMVar_hsa_circ_166137,RMVar_hsa_circ_344812,RMVar_hsa_circ_166138,RMVar_hsa_circ_365935,RMVar_hsa_circ_322673,RMVar_hsa_circ_363396 25811 RMVar_ID_25811 Human_SNP_ID_551937185 A-to-I Human chr14 + 39324973 39324973 39324973 CACTGGGTGCAGTGGCTTACAACTATAATCCTAGTACTTTGGGAGGTCAAGGTGGTGGGATTGTT CACTGGGTGCAGTGGCTTACAACTATAATCCTGGTACTTTGGGAGGTCAAGGTGGTGGGATTGTT A G MIA2 Ensembl:ENSG00000150527 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1403993501 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17562536 RMVar_hsa_circ_55578,RMVar_hsa_circ_357844,RMVar_hsa_circ_279700,RMVar_hsa_circ_284519,RMVar_hsa_circ_83225,RMVar_hsa_circ_166126,RMVar_hsa_circ_166127,RMVar_hsa_circ_13978,RMVar_hsa_circ_166132,RMVar_hsa_circ_334404,RMVar_hsa_circ_345510,RMVar_hsa_circ_166134,RMVar_hsa_circ_62818,RMVar_hsa_circ_17846,RMVar_hsa_circ_66339,RMVar_hsa_circ_93576,RMVar_hsa_circ_166135,RMVar_hsa_circ_358623,RMVar_hsa_circ_55553,RMVar_hsa_circ_302859,RMVar_hsa_circ_33419,RMVar_hsa_circ_290726,RMVar_hsa_circ_166136,RMVar_hsa_circ_289144,RMVar_hsa_circ_308040,RMVar_hsa_circ_166137,RMVar_hsa_circ_344812,RMVar_hsa_circ_166138,RMVar_hsa_circ_365935,RMVar_hsa_circ_322673,RMVar_hsa_circ_363396 25812 RMVar_ID_25812 Human_SNP_ID_551937210 A-to-I Human chr14 + 39325079 39325078 39325080 ACCCTGTATCTACAAAAAATACAACAATTAACAAAGCGTGGTGGCACATGCCTGTTGTCCCAGCT ACCCTGTATCTACAAAAAATACAACAATTAAC__AGCGTGGTGGCACATGCCTGTTGTCCCAGCT CAA C MIA2 Ensembl:ENSG00000150527 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1299197270 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_17848400 RMVar_hsa_circ_55578,RMVar_hsa_circ_357844,RMVar_hsa_circ_279700,RMVar_hsa_circ_284519,RMVar_hsa_circ_83225,RMVar_hsa_circ_166126,RMVar_hsa_circ_166127,RMVar_hsa_circ_13978,RMVar_hsa_circ_166132,RMVar_hsa_circ_334404,RMVar_hsa_circ_345510,RMVar_hsa_circ_166134,RMVar_hsa_circ_62818,RMVar_hsa_circ_17846,RMVar_hsa_circ_66339,RMVar_hsa_circ_93576,RMVar_hsa_circ_166135,RMVar_hsa_circ_358623,RMVar_hsa_circ_55553,RMVar_hsa_circ_302859,RMVar_hsa_circ_33419,RMVar_hsa_circ_290726,RMVar_hsa_circ_166136,RMVar_hsa_circ_289144,RMVar_hsa_circ_308040,RMVar_hsa_circ_166137,RMVar_hsa_circ_344812,RMVar_hsa_circ_166138,RMVar_hsa_circ_365935,RMVar_hsa_circ_322673,RMVar_hsa_circ_363396 25813 RMVar_ID_25813 Human_SNP_ID_551937210 A-to-I Human chr14 + 39325080 39325078 39325080 CCCTGTATCTACAAAAAATACAACAATTAACAAAGCGTGGTGGCACATGCCTGTTGTCCCAGCTA CCCTGTATCTACAAAAAATACAACAATTAAC__AGCGTGGTGGCACATGCCTGTTGTCCCAGCTA CAA C MIA2 Ensembl:ENSG00000150527 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1299197270 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_17848400 RMVar_hsa_circ_55578,RMVar_hsa_circ_357844,RMVar_hsa_circ_279700,RMVar_hsa_circ_284519,RMVar_hsa_circ_83225,RMVar_hsa_circ_166126,RMVar_hsa_circ_166127,RMVar_hsa_circ_13978,RMVar_hsa_circ_166132,RMVar_hsa_circ_334404,RMVar_hsa_circ_345510,RMVar_hsa_circ_166134,RMVar_hsa_circ_62818,RMVar_hsa_circ_17846,RMVar_hsa_circ_66339,RMVar_hsa_circ_93576,RMVar_hsa_circ_166135,RMVar_hsa_circ_358623,RMVar_hsa_circ_55553,RMVar_hsa_circ_302859,RMVar_hsa_circ_33419,RMVar_hsa_circ_290726,RMVar_hsa_circ_166136,RMVar_hsa_circ_289144,RMVar_hsa_circ_308040,RMVar_hsa_circ_166137,RMVar_hsa_circ_344812,RMVar_hsa_circ_166138,RMVar_hsa_circ_365935,RMVar_hsa_circ_322673,RMVar_hsa_circ_363396 25814 RMVar_ID_25814 Human_SNP_ID_551937211 A-to-I Human chr14 + 39325080 39325080 39325080 CCCTGTATCTACAAAAAATACAACAATTAACAAAGCGTGGTGGCACATGCCTGTTGTCCCAGCTA CCCTGTATCTACAAAAAATACAACAATTAACAGAGCGTGGTGGCACATGCCTGTTGTCCCAGCTA A G MIA2 Ensembl:ENSG00000150527 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1399574234 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17848400 RMVar_hsa_circ_55578,RMVar_hsa_circ_357844,RMVar_hsa_circ_279700,RMVar_hsa_circ_284519,RMVar_hsa_circ_83225,RMVar_hsa_circ_166126,RMVar_hsa_circ_166127,RMVar_hsa_circ_13978,RMVar_hsa_circ_166132,RMVar_hsa_circ_334404,RMVar_hsa_circ_345510,RMVar_hsa_circ_166134,RMVar_hsa_circ_62818,RMVar_hsa_circ_17846,RMVar_hsa_circ_66339,RMVar_hsa_circ_93576,RMVar_hsa_circ_166135,RMVar_hsa_circ_358623,RMVar_hsa_circ_55553,RMVar_hsa_circ_302859,RMVar_hsa_circ_33419,RMVar_hsa_circ_290726,RMVar_hsa_circ_166136,RMVar_hsa_circ_289144,RMVar_hsa_circ_308040,RMVar_hsa_circ_166137,RMVar_hsa_circ_344812,RMVar_hsa_circ_166138,RMVar_hsa_circ_365935,RMVar_hsa_circ_322673,RMVar_hsa_circ_363396 25815 RMVar_ID_25815 Human_SNP_ID_551937223 A-to-I Human chr14 + 39325112 39325112 39325112 AAGCGTGGTGGCACATGCCTGTTGTCCCAGCTACTTGTAAGGCTGAGGTGGGAGAATTGCTTGAG AAGCGTGGTGGCACATGCCTGTTGTCCCAGCTGCTTGTAAGGCTGAGGTGGGAGAATTGCTTGAG A G MIA2 Ensembl:ENSG00000150527 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1238885245 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55578,RMVar_hsa_circ_357844,RMVar_hsa_circ_279700,RMVar_hsa_circ_284519,RMVar_hsa_circ_83225,RMVar_hsa_circ_166126,RMVar_hsa_circ_166127,RMVar_hsa_circ_13978,RMVar_hsa_circ_166132,RMVar_hsa_circ_334404,RMVar_hsa_circ_345510,RMVar_hsa_circ_166134,RMVar_hsa_circ_62818,RMVar_hsa_circ_17846,RMVar_hsa_circ_66339,RMVar_hsa_circ_93576,RMVar_hsa_circ_166135,RMVar_hsa_circ_358623,RMVar_hsa_circ_55553,RMVar_hsa_circ_302859,RMVar_hsa_circ_33419,RMVar_hsa_circ_290726,RMVar_hsa_circ_166136,RMVar_hsa_circ_289144,RMVar_hsa_circ_308040,RMVar_hsa_circ_166137,RMVar_hsa_circ_344812,RMVar_hsa_circ_166138,RMVar_hsa_circ_365935,RMVar_hsa_circ_322673,RMVar_hsa_circ_363396 25816 RMVar_ID_25816 Human_SNP_ID_551937294 A-to-I Human chr14 + 39325292 39325292 39325292 AGAATAATAAGCTTTTGTTTTCTGGACAATATAATTTTGAGAAGACCCCCCTTTTCCCTCTCAAT AGAATAATAAGCTTTTGTTTTCTGGACAATATGATTTTGAGAAGACCCCCCTTTTCCCTCTCAAT A G MIA2 Ensembl:ENSG00000150527 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs12897272 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55578,RMVar_hsa_circ_357844,RMVar_hsa_circ_279700,RMVar_hsa_circ_284519,RMVar_hsa_circ_83225,RMVar_hsa_circ_166126,RMVar_hsa_circ_166127,RMVar_hsa_circ_13978,RMVar_hsa_circ_166132,RMVar_hsa_circ_334404,RMVar_hsa_circ_345510,RMVar_hsa_circ_166134,RMVar_hsa_circ_62818,RMVar_hsa_circ_17846,RMVar_hsa_circ_66339,RMVar_hsa_circ_93576,RMVar_hsa_circ_166135,RMVar_hsa_circ_358623,RMVar_hsa_circ_55553,RMVar_hsa_circ_302859,RMVar_hsa_circ_33419,RMVar_hsa_circ_290726,RMVar_hsa_circ_166136,RMVar_hsa_circ_289144,RMVar_hsa_circ_308040,RMVar_hsa_circ_166137,RMVar_hsa_circ_344812,RMVar_hsa_circ_166138,RMVar_hsa_circ_365935,RMVar_hsa_circ_322673,RMVar_hsa_circ_363396 25817 RMVar_ID_25817 Human_SNP_ID_551937295 A-to-I Human chr14 + 39325292 39325292 39325292 AGAATAATAAGCTTTTGTTTTCTGGACAATATAATTTTGAGAAGACCCCCCTTTTCCCTCTCAAT AGAATAATAAGCTTTTGTTTTCTGGACAATATTATTTTGAGAAGACCCCCCTTTTCCCTCTCAAT A T MIA2 Ensembl:ENSG00000150527 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs12897272 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55578,RMVar_hsa_circ_357844,RMVar_hsa_circ_279700,RMVar_hsa_circ_284519,RMVar_hsa_circ_83225,RMVar_hsa_circ_166126,RMVar_hsa_circ_166127,RMVar_hsa_circ_13978,RMVar_hsa_circ_166132,RMVar_hsa_circ_334404,RMVar_hsa_circ_345510,RMVar_hsa_circ_166134,RMVar_hsa_circ_62818,RMVar_hsa_circ_17846,RMVar_hsa_circ_66339,RMVar_hsa_circ_93576,RMVar_hsa_circ_166135,RMVar_hsa_circ_358623,RMVar_hsa_circ_55553,RMVar_hsa_circ_302859,RMVar_hsa_circ_33419,RMVar_hsa_circ_290726,RMVar_hsa_circ_166136,RMVar_hsa_circ_289144,RMVar_hsa_circ_308040,RMVar_hsa_circ_166137,RMVar_hsa_circ_344812,RMVar_hsa_circ_166138,RMVar_hsa_circ_365935,RMVar_hsa_circ_322673,RMVar_hsa_circ_363396 25818 RMVar_ID_25818 Human_SNP_ID_551937354 A-to-I Human chr14 + 39325429 39325429 39325429 TCGCTCTATCCCCCAGACTGGTGTGCAGTGGCATGATCTTGGCTCACTGCAACCTCCTCCTCCTG TCGCTCTATCCCCCAGACTGGTGTGCAGTGGCGTGATCTTGGCTCACTGCAACCTCCTCCTCCTG A G MIA2 Ensembl:ENSG00000150527 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs964638441 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12460671 RMVar_hsa_circ_55578,RMVar_hsa_circ_357844,RMVar_hsa_circ_279700,RMVar_hsa_circ_284519,RMVar_hsa_circ_83225,RMVar_hsa_circ_166126,RMVar_hsa_circ_166127,RMVar_hsa_circ_13978,RMVar_hsa_circ_166132,RMVar_hsa_circ_334404,RMVar_hsa_circ_345510,RMVar_hsa_circ_166134,RMVar_hsa_circ_62818,RMVar_hsa_circ_17846,RMVar_hsa_circ_66339,RMVar_hsa_circ_93576,RMVar_hsa_circ_166135,RMVar_hsa_circ_358623,RMVar_hsa_circ_55553,RMVar_hsa_circ_302859,RMVar_hsa_circ_33419,RMVar_hsa_circ_290726,RMVar_hsa_circ_166136,RMVar_hsa_circ_289144,RMVar_hsa_circ_308040,RMVar_hsa_circ_166137,RMVar_hsa_circ_344812,RMVar_hsa_circ_166138,RMVar_hsa_circ_365935,RMVar_hsa_circ_322673,RMVar_hsa_circ_363396 25819 RMVar_ID_25819 Human_SNP_ID_551937564 A-to-I Human chr14 + 39325934 39325934 39325934 CAGGGTTTCACCATGTTGGCCAGGCTTGTCTCAAATTCCTGATCTCAGGTGGTCCACCCTCCTCG CAGGGTTTCACCATGTTGGCCAGGCTTGTCTCGAATTCCTGATCTCAGGTGGTCCACCCTCCTCG A G MIA2 Ensembl:ENSG00000150527 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1239820080 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55578,RMVar_hsa_circ_357844,RMVar_hsa_circ_279700,RMVar_hsa_circ_284519,RMVar_hsa_circ_83225,RMVar_hsa_circ_166126,RMVar_hsa_circ_166127,RMVar_hsa_circ_13978,RMVar_hsa_circ_166132,RMVar_hsa_circ_334404,RMVar_hsa_circ_345510,RMVar_hsa_circ_166134,RMVar_hsa_circ_62818,RMVar_hsa_circ_17846,RMVar_hsa_circ_66339,RMVar_hsa_circ_93576,RMVar_hsa_circ_166135,RMVar_hsa_circ_358623,RMVar_hsa_circ_55553,RMVar_hsa_circ_302859,RMVar_hsa_circ_33419,RMVar_hsa_circ_290726,RMVar_hsa_circ_166136,RMVar_hsa_circ_289144,RMVar_hsa_circ_308040,RMVar_hsa_circ_166137,RMVar_hsa_circ_344812,RMVar_hsa_circ_166138,RMVar_hsa_circ_365935,RMVar_hsa_circ_322673,RMVar_hsa_circ_363396 25820 RMVar_ID_25820 Human_SNP_ID_551980188 A-to-I Human chr14 + 39485761 39485761 39485761 GTAGGTTAGATAATCTGTAGTAGCATAGCAGTAGCTAGTTCAGCCTTGGTGAGAGAGAGCCCATA GTAGGTTAGATAATCTGTAGTAGCATAGCAGTCGCTAGTTCAGCCTTGGTGAGAGAGAGCCCATA A C AL049828.1 Ensembl:ENSG00000258526 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1469452689 Functional Loss SNV dbSNP153 33..33 33 - - - 25821 RMVar_ID_25821 Human_SNP_ID_551986140 A-to-I Human chr14 + 39508962 39508962 39508962 AAACATATAAAAAATTGTCAACATCACTAATTATCAGGAAATGCAAATTAAAATTGCATTGTGAT AAACATATAAAAAATTGTCAACATCACTAATTTTCAGGAAATGCAAATTAAAATTGCATTGTGAT A T AL049828.1 Ensembl:ENSG00000258526 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1225046689 Functional Loss SNV dbSNP153 33..33 33 - - - 25822 RMVar_ID_25822 Human_SNP_ID_551989950 A-to-I Human chr14 + 39519751 39519751 39519751 AAAGACAAATAACCCTATTAAAAAGTAGGCAAAAGACATGAACAGATACTTTTCAAAAGAAGGCA AAAGACAAATAACCCTATTAAAAAGTAGGCAAGAGACATGAACAGATACTTTTCAAAAGAAGGCA A G AL049828.1 Ensembl:ENSG00000258526 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1290416537 Functional Loss SNV dbSNP153 33..33 33 - - - 25823 RMVar_ID_25823 Human_SNP_ID_551990441 A-to-I Human chr14 + 39521055 39521055 39521055 TTGATTTCCTTTCTTTTGGATATGTTCCAAGTAGTAGAATTGTTGGATCATATAGTAGTTCTATT TTGATTTCCTTTCTTTTGGATATGTTCCAAGTGGTAGAATTGTTGGATCATATAGTAGTTCTATT A G AL049828.1 Ensembl:ENSG00000258526 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1191532003 Functional Loss SNV dbSNP153 33..33 33 - - - 25824 RMVar_ID_25824 Human_SNP_ID_551997748 A-to-I Human chr14 + 39542291 39542291 39542291 AATACTGCAGTTCTCACTTATAAGAGGGAGTTAAATGATGAGAACTCATGGACATAAAGAGAGGA AATACTGCAGTTCTCACTTATAAGAGGGAGTTCAATGATGAGAACTCATGGACATAAAGAGAGGA A C AL049828.1 Ensembl:ENSG00000258526 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1242326343 Functional Loss SNV dbSNP153 33..33 33 - - - 25825 RMVar_ID_25825 Human_SNP_ID_552538236 A-to-I Human chr14 + 41683988 41683988 41683988 TTATGTGGAACCTCAGAAGACCCAGAATATCCAAAGCTGTCATGAACAGAAAGAATAAAACTGGT TTATGTGGAACCTCAGAAGACCCAGAATATCCGAAGCTGTCATGAACAGAAAGAATAAAACTGGT A G LRFN5 Ensembl:ENSG00000165379 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs182226260 Functional Loss SNV dbSNP153 33..33 33 - - - 25826 RMVar_ID_25826 Human_SNP_ID_552538884 A-to-I Human chr14 + 41686782 41686782 41686782 GATGGATTACATTTAATGATGTGCATATGTTGAAGCAGTCTTGCATCCCAGGGATGAAGCTGACT GATGGATTACATTTAATGATGTGCATATGTTGTAGCAGTCTTGCATCCCAGGGATGAAGCTGACT A T LRFN5 Ensembl:ENSG00000165379 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs926173052 Functional Loss SNV dbSNP153 33..33 33 - - - 25827 RMVar_ID_25827 Human_SNP_ID_553192232 A-to-I Human chr14 - 44120555 44120553 44120555 GGAGATTGCAAATCAACGTCTCACTTCCAAACAGGGGAAGAAGACAAGAAAATTAATGTAGAACT GGAGATTGCAAATCAACGTCTCACTTCCAAAC__GGGAAGAAGACAAGAAAATTAATGTAGAACT CCT C LINC02307,AL109766.1 Ensembl:ENSG00000258969,Ensembl:ENSG00000259137 lincRNA,Pseudogene intron,exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1218524945 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_5563634,Human_RBP_ID_8250652,Human_RBP_ID_17364164,Human_RBP_ID_18528617 25828 RMVar_ID_25828 Human_SNP_ID_553192233 A-to-I Human chr14 - 44120555 44120555 44120555 GGAGATTGCAAATCAACGTCTCACTTCCAAACAGGGGAAGAAGACAAGAAAATTAATGTAGAACT GGAGATTGCAAATCAACGTCTCACTTCCAAACGGGGGAAGAAGACAAGAAAATTAATGTAGAACT T C LINC02307,AL109766.1 Ensembl:ENSG00000258969,Ensembl:ENSG00000259137 lincRNA,Pseudogene intron,exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs879135622 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5563634,Human_RBP_ID_8250652,Human_RBP_ID_17364164,Human_RBP_ID_18528617 25829 RMVar_ID_25829 Human_SNP_ID_553192234 A-to-I Human chr14 - 44120555 44120555 44120555 GGAGATTGCAAATCAACGTCTCACTTCCAAACAGGGGAAGAAGACAAGAAAATTAATGTAGAACT GGAGATTGCAAATCAACGTCTCACTTCCAAACCGGGGAAGAAGACAAGAAAATTAATGTAGAACT T G LINC02307,AL109766.1 Ensembl:ENSG00000258969,Ensembl:ENSG00000259137 lincRNA,Pseudogene intron,exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs879135622 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5563634,Human_RBP_ID_8250652,Human_RBP_ID_17364164,Human_RBP_ID_18528617 25830 RMVar_ID_25830 Human_SNP_ID_553192277 A-to-I Human chr14 + 44120702 44120702 44120702 TCTGCTGCCTCCCAATTGCTAGATCCCAGATCATCATCTGGGGAGGCTGAACACTTCACCCCATG TCTGCTGCCTCCCAATTGCTAGATCCCAGATCGTCATCTGGGGAGGCTGAACACTTCACCCCATG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878921136 Functional Loss SNV dbSNP153 33..33 33 - - - 25831 RMVar_ID_25831 Human_SNP_ID_553192280 A-to-I Human chr14 + 44120705 44120705 44120705 GCTGCCTCCCAATTGCTAGATCCCAGATCATCATCTGGGGAGGCTGAACACTTCACCCCATGCAG GCTGCCTCCCAATTGCTAGATCCCAGATCATCGTCTGGGGAGGCTGAACACTTCACCCCATGCAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878924169 Functional Loss SNV dbSNP153 33..33 33 - - - 25832 RMVar_ID_25832 Human_SNP_ID_553192288 A-to-I Human chr14 + 44120722 44120722 44120722 AGATCCCAGATCATCATCTGGGGAGGCTGAACACTTCACCCCATGCAGGTGAGACTCTCTGGCAG AGATCCCAGATCATCATCTGGGGAGGCTGAACCCTTCACCCCATGCAGGTGAGACTCTCTGGCAG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878962870 Functional Loss SNV dbSNP153 33..33 33 - - - 25833 RMVar_ID_25833 Human_SNP_ID_553192289 A-to-I Human chr14 + 44120722 44120722 44120722 AGATCCCAGATCATCATCTGGGGAGGCTGAACACTTCACCCCATGCAGGTGAGACTCTCTGGCAG AGATCCCAGATCATCATCTGGGGAGGCTGAACGCTTCACCCCATGCAGGTGAGACTCTCTGGCAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878962870 Functional Loss SNV dbSNP153 33..33 33 - - - 25834 RMVar_ID_25834 Human_SNP_ID_553385473 A-to-I Human chr14 - 44861460 44861458 44861461 GCTGGGATGATGGATGTCCATTATAGTGAAGAAGTTTTGCTGGAGTTGCTAGAACAATGTGTGGA GCTGGGATGATGGATGTCCATTATAGTGAAG___TTTTGCTGGAGTTGCTAGAACAATGTGTGGA ACTT A DOCK11P1 Ensembl:ENSG00000259000 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1442594431 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_5563796 25835 RMVar_ID_25835 Human_SNP_ID_553403603 A-to-I Human chr14 - 44923309 44923309 44923309 TTGGCCAGGGTGTTCTGGAACTCCTTGCCTCAAGTCATCCTCCCACCTCGGCCTCTGAAAGTGCT TTGGCCAGGGTGTTCTGGAACTCCTTGCCTCAGGTCATCCTCCCACCTCGGCCTCTGAAAGTGCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1410617156 Functional Loss SNV dbSNP153 33..33 33 - - - 25836 RMVar_ID_25836 Human_SNP_ID_553403639 A-to-I Human chr14 - 44923446 44923446 44923446 CACTCACTGCAGCCTCCATTTCTTGGACTCAAATGATCCTACTGCCTCAGCCTCCTGAGTAGCTG CACTCACTGCAGCCTCCATTTCTTGGACTCAATTGATCCTACTGCCTCAGCCTCCTGAGTAGCTG T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1340099887 Functional Loss SNV dbSNP153 33..33 33 - - - 25837 RMVar_ID_25837 Human_SNP_ID_230263288 A-to-I Human chr5 - 45256870 45256870 45256870 ATTTTGGCTAAAATAAAGCAAGTTCTCAGGCCAGGCGTGGTGGCTCATGCCTGTAATCCTAGCAC ATTTTGGCTAAAATAAAGCAAGTTCTCAGGCCGGGCGTGGTGGCTCATGCCTGTAATCCTAGCAC T C HCN1 Ensembl:ENSG00000164588 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1456089201 Functional Loss SNV dbSNP153 33..33 33 - - - 25838 RMVar_ID_25838 Human_SNP_ID_231290564 A-to-I Human chr5 - 50396446 50396446 50396446 ACCATCTTACATGCTTAAATAACTCCACATTTATTTGTGTTTATTACTCTGTGTTATAAATATAC ACCATCTTACATGCTTAAATAACTCCACATTTTTTTGTGTTTATTACTCTGTGTTATAAATATAC T A EMB Ensembl:ENSG00000170571 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1341652661 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3771549,Human_RBP_ID_7503959,Human_RBP_ID_21172695,Human_RBP_ID_26703362 25839 RMVar_ID_25839 Human_SNP_ID_231410073 A-to-I Human chr5 + 50843874 50843874 50843874 TTTGAAATTAGTCTATACGTTAGACAGTCTATACATGACAAACATGAAGATCTAATATCAAGATT TTTGAAATTAGTCTATACGTTAGACAGTCTATGCATGACAAACATGAAGATCTAATATCAAGATT A G PARP8 Ensembl:ENSG00000151883 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1446547145 Functional Loss SNV dbSNP153 33..33 33 - - - 25840 RMVar_ID_25840 Human_SNP_ID_231941676 A-to-I Human chr5 - 52889230 52889230 52889230 AAGTGTGGTGGTGTGCGCCTGTGGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATTGCTTGAT AAGTGTGGTGGTGTGCGCCTGTGGTCCCAGCTCCTTGGGAGGCTGAGGCAGGAGAATTGCTTGAT T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1185418747 Functional Loss SNV dbSNP153 33..33 33 - - - 25841 RMVar_ID_25841 Human_SNP_ID_231993105 A-to-I Human chr5 - 53098629 53098628 53098630 TACGAAGAGTCATCAACTTGGAAAGGAAACAAAGAGTGCTTTTGGGCATCCAACAGTTAATCACT TACGAAGAGTCATCAACTTGGAAAGGAAACA__GAGTGCTTTTGGGCATCCAACAGTTAATCACT CTT C MOCS2 Ensembl:ENSG00000164172 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs398122797 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_643168 Human_Splice_Rec_650348,Human_Splice_Rec_650358,Human_Splice_Rec_650364,Human_Splice_Rec_650376,Human_Splice_Rec_650388,Human_Splice_Rec_650398,Human_Splice_Rec_650406,Human_Splice_Rec_650416 Clinvar_Rec_95 25842 RMVar_ID_25842 Human_SNP_ID_232113441 A-to-I Human chr5 + 53563541 53563541 53563541 TTTTTTTTTGGAGATGTAGTTTCGCTCTTGTCACCCATTCTAGAGTGCAGTGGCACAATCTCAGT TTTTTTTTTGGAGATGTAGTTTCGCTCTTGTCCCCCATTCTAGAGTGCAGTGGCACAATCTCAGT A C NDUFS4 Ensembl:ENSG00000164258 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559884923 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15457199 RMVar_hsa_circ_231352,RMVar_hsa_circ_80678,RMVar_hsa_circ_90741,RMVar_hsa_circ_231353 25843 RMVar_ID_25843 Human_SNP_ID_232232317 A-to-I Human chr5 - 54032433 54032433 54032433 GTCAGGAGTTTGAGACCAGCCTGGCCAACATGATGAAACCCTGTCTGTGCTAAAAATACAAAAAT GTCAGGAGTTTGAGACCAGCCTGGCCAACATGGTGAAACCCTGTCTGTGCTAAAAATACAAAAAT T C ARL15 Ensembl:ENSG00000185305 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1297486769 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114374,RMVar_hsa_circ_231367,RMVar_hsa_circ_231366 25844 RMVar_ID_25844 Human_SNP_ID_232241200 A-to-I Human chr5 - 54069508 54069508 54069508 CACCCAGGCTGGCGTGATCTGGACTCACTGCAACCTCCACCTCCCAGGTTCAAGTGATTCTCCTG CACCCAGGCTGGCGTGATCTGGACTCACTGCACCCTCCACCTCCCAGGTTCAAGTGATTCTCCTG T G ARL15 Ensembl:ENSG00000185305 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs998617439 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114374,RMVar_hsa_circ_231366 25845 RMVar_ID_25845 Human_SNP_ID_232556280 A-to-I Human chr5 + 55367365 55367365 55367365 AAAATGAGCTGGGCATGGTGGTGGGCTTCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA AAAATGAGCTGGGCATGGTGGTGGGCTTCTGTGGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA A G MTREX Ensembl:ENSG00000039123 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1315079356 Functional Loss SNV dbSNP153 33..33 33 - - - 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_10290,RMVar_hsa_circ_306042,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_297257,RMVar_hsa_circ_231415,RMVar_hsa_circ_231416,RMVar_hsa_circ_231426,RMVar_hsa_circ_27044,RMVar_hsa_circ_286698,RMVar_hsa_circ_126461,RMVar_hsa_circ_121598,RMVar_hsa_circ_231428,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_338978,RMVar_hsa_circ_60619,RMVar_hsa_circ_37695,RMVar_hsa_circ_231440,RMVar_hsa_circ_297755,RMVar_hsa_circ_286436,RMVar_hsa_circ_351013,RMVar_hsa_circ_67412,RMVar_hsa_circ_231441 25846 RMVar_ID_25846 Human_SNP_ID_232565966 A-to-I Human chr5 + 55407947 55407947 55407947 GGCTAATTTCTTTTTTAAGTTTCTGTAGAGATAGGGTCTTGCTATGTTGCCCAGGCTGGTCTTGA GGCTAATTTCTTTTTTAAGTTTCTGTAGAGATGGGGTCTTGCTATGTTGCCCAGGCTGGTCTTGA A G MTREX Ensembl:ENSG00000039123 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049662838 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45085,RMVar_hsa_circ_16682,RMVar_hsa_circ_231413,RMVar_hsa_circ_366330,RMVar_hsa_circ_118109,RMVar_hsa_circ_55082,RMVar_hsa_circ_231435,RMVar_hsa_circ_231443,RMVar_hsa_circ_43340,RMVar_hsa_circ_60619,RMVar_hsa_circ_37695,RMVar_hsa_circ_58113,RMVar_hsa_circ_74885,RMVar_hsa_circ_359398 25847 RMVar_ID_25847 Human_SNP_ID_232586519 A-to-I Human chr5 - 55491673 55491671 55491673 TTGTGTTGTTAGTAGAGACGGGGTTTCATCATATTGGCCAGGCTCGTCTTGAACTCTTCATGTCA TTGTGTTGTTAGTAGAGACGGGGTTTCATCAT__TGGCCAGGCTCGTCTTGAACTCTTCATGTCA AAT A PLPP1 Ensembl:ENSG00000067113 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1278617208 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_85013,RMVar_hsa_circ_231447 25848 RMVar_ID_25848 Human_SNP_ID_232586520 A-to-I Human chr5 - 55491673 55491673 55491673 TTGTGTTGTTAGTAGAGACGGGGTTTCATCATATTGGCCAGGCTCGTCTTGAACTCTTCATGTCA TTGTGTTGTTAGTAGAGACGGGGTTTCATCATGTTGGCCAGGCTCGTCTTGAACTCTTCATGTCA T C PLPP1 Ensembl:ENSG00000067113 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1368680316 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85013,RMVar_hsa_circ_231447 25849 RMVar_ID_25849 Human_SNP_ID_232589425 A-to-I Human chr5 - 55503596 55503596 55503596 TTTGTATTTTTTTTTAGCAGAGATGGGGTTTTACCATGTTGGCCAGTTTGGTCTTGAGCTCCTGA TTTGTATTTTTTTTTAGCAGAGATGGGGTTTTGCCATGTTGGCCAGTTTGGTCTTGAGCTCCTGA T C PLPP1 Ensembl:ENSG00000067113 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474055407 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85013,RMVar_hsa_circ_231447 25850 RMVar_ID_25850 Human_SNP_ID_232589875 A-to-I Human chr5 - 55504951 55504951 55504951 CAAAAATTAGCCGGGTGTGGTGATGTGCACCTATAGTTCAAGCTACTCAGAAGGCTATGGTGGGA CAAAAATTAGCCGGGTGTGGTGATGTGCACCTGTAGTTCAAGCTACTCAGAAGGCTATGGTGGGA T C PLPP1 Ensembl:ENSG00000067113 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1462494238 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85013,RMVar_hsa_circ_231447 25851 RMVar_ID_25851 Human_SNP_ID_232592046 A-to-I Human chr5 - 55513372 55513372 55513372 CCTGTAGTCCCAGATACCCTGGAAGCTGAGGCAGGAGAATCGCTTGAACCCTGGAGGCAGAGGTT CCTGTAGTCCCAGATACCCTGGAAGCTGAGGCGGGAGAATCGCTTGAACCCTGGAGGCAGAGGTT T C PLPP1 Ensembl:ENSG00000067113 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048038893 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85013,RMVar_hsa_circ_231447 25852 RMVar_ID_25852 Human_SNP_ID_232624288 A-to-I Human chr5 - 55646203 55646203 55646203 CCACGCTAATTTTTGTATTTTTAGTAAAGACAAGGTTTCGCCATGTTGGCCAGGCTGGTCTCAAA CCACGCTAATTTTTGTATTTTTAGTAAAGACAGGGTTTCGCCATGTTGGCCAGGCTGGTCTCAAA T C SLC38A9 Ensembl:ENSG00000177058 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1446536575 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34142,RMVar_hsa_circ_231462,RMVar_hsa_circ_8900,RMVar_hsa_circ_52707,RMVar_hsa_circ_276303,RMVar_hsa_circ_15543,RMVar_hsa_circ_311864,RMVar_hsa_circ_324840,RMVar_hsa_circ_309770,RMVar_hsa_circ_10814,RMVar_hsa_circ_43646,RMVar_hsa_circ_231457,RMVar_hsa_circ_231458,RMVar_hsa_circ_62574,RMVar_hsa_circ_21222,RMVar_hsa_circ_34011,RMVar_hsa_circ_14621,RMVar_hsa_circ_279867,RMVar_hsa_circ_310266,RMVar_hsa_circ_341314,RMVar_hsa_circ_231459,RMVar_hsa_circ_366152,RMVar_hsa_circ_310579,RMVar_hsa_circ_289122,RMVar_hsa_circ_301751,RMVar_hsa_circ_280109,RMVar_hsa_circ_6564,RMVar_hsa_circ_15175,RMVar_hsa_circ_231464,RMVar_hsa_circ_231465,RMVar_hsa_circ_231463,RMVar_hsa_circ_231460,RMVar_hsa_circ_231461 25853 RMVar_ID_25853 Human_SNP_ID_232624289 A-to-I Human chr5 - 55646208 55646208 55646208 CACCACCACGCTAATTTTTGTATTTTTAGTAAAGACAAGGTTTCGCCATGTTGGCCAGGCTGGTC CACCACCACGCTAATTTTTGTATTTTTAGTAAGGACAAGGTTTCGCCATGTTGGCCAGGCTGGTC T C SLC38A9 Ensembl:ENSG00000177058 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs960030018 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34142,RMVar_hsa_circ_231462,RMVar_hsa_circ_8900,RMVar_hsa_circ_52707,RMVar_hsa_circ_276303,RMVar_hsa_circ_15543,RMVar_hsa_circ_311864,RMVar_hsa_circ_324840,RMVar_hsa_circ_309770,RMVar_hsa_circ_10814,RMVar_hsa_circ_43646,RMVar_hsa_circ_231457,RMVar_hsa_circ_231458,RMVar_hsa_circ_62574,RMVar_hsa_circ_21222,RMVar_hsa_circ_34011,RMVar_hsa_circ_14621,RMVar_hsa_circ_279867,RMVar_hsa_circ_310266,RMVar_hsa_circ_341314,RMVar_hsa_circ_231459,RMVar_hsa_circ_366152,RMVar_hsa_circ_310579,RMVar_hsa_circ_289122,RMVar_hsa_circ_301751,RMVar_hsa_circ_280109,RMVar_hsa_circ_6564,RMVar_hsa_circ_15175,RMVar_hsa_circ_231464,RMVar_hsa_circ_231465,RMVar_hsa_circ_231463,RMVar_hsa_circ_231460,RMVar_hsa_circ_231461 25854 RMVar_ID_25854 Human_SNP_ID_232624431 A-to-I Human chr5 - 55646871 55646871 55646871 TGGCATGCACCTATAATCCTAGTTACCAGGGAAGCTGAGATAGGAATATCACTTGAGCCCAGAAA TGGCATGCACCTATAATCCTAGTTACCAGGGAGGCTGAGATAGGAATATCACTTGAGCCCAGAAA T C SLC38A9 Ensembl:ENSG00000177058 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417333274 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34142,RMVar_hsa_circ_231462,RMVar_hsa_circ_8900,RMVar_hsa_circ_52707,RMVar_hsa_circ_276303,RMVar_hsa_circ_15543,RMVar_hsa_circ_311864,RMVar_hsa_circ_324840,RMVar_hsa_circ_309770,RMVar_hsa_circ_10814,RMVar_hsa_circ_43646,RMVar_hsa_circ_231457,RMVar_hsa_circ_231458,RMVar_hsa_circ_62574,RMVar_hsa_circ_21222,RMVar_hsa_circ_34011,RMVar_hsa_circ_14621,RMVar_hsa_circ_279867,RMVar_hsa_circ_310266,RMVar_hsa_circ_341314,RMVar_hsa_circ_231459,RMVar_hsa_circ_366152,RMVar_hsa_circ_310579,RMVar_hsa_circ_289122,RMVar_hsa_circ_301751,RMVar_hsa_circ_280109,RMVar_hsa_circ_6564,RMVar_hsa_circ_15175,RMVar_hsa_circ_231464,RMVar_hsa_circ_231465,RMVar_hsa_circ_231463,RMVar_hsa_circ_231460,RMVar_hsa_circ_231461 25855 RMVar_ID_25855 Human_SNP_ID_232633992 A-to-I Human chr5 - 55687809 55687809 55687809 CCTATAGTCCCAGCACTCGGGAGGCTGAGGCCAGAGAATCTCTTGAACCCAAGAGGCGGAGGTTG CCTATAGTCCCAGCACTCGGGAGGCTGAGGCCTGAGAATCTCTTGAACCCAAGAGGCGGAGGTTG T A SLC38A9 Ensembl:ENSG00000177058 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1228409570 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7816,RMVar_hsa_circ_43646,RMVar_hsa_circ_310266,RMVar_hsa_circ_341314,RMVar_hsa_circ_366152,RMVar_hsa_circ_231465,RMVar_hsa_circ_26142,RMVar_hsa_circ_231470,RMVar_hsa_circ_30309,RMVar_hsa_circ_16948,RMVar_hsa_circ_12111,RMVar_hsa_circ_15857,RMVar_hsa_circ_59397,RMVar_hsa_circ_46709,RMVar_hsa_circ_231476,RMVar_hsa_circ_313972,RMVar_hsa_circ_231479 25856 RMVar_ID_25856 Human_SNP_ID_232633999 A-to-I Human chr5 - 55687836 55687836 55687836 AAAATTAGCCGGACATGGTGACACGCACCTATAGTCCCAGCACTCGGGAGGCTGAGGCCAGAGAA AAAATTAGCCGGACATGGTGACACGCACCTATGGTCCCAGCACTCGGGAGGCTGAGGCCAGAGAA T C SLC38A9 Ensembl:ENSG00000177058 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1475954158 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7816,RMVar_hsa_circ_43646,RMVar_hsa_circ_310266,RMVar_hsa_circ_341314,RMVar_hsa_circ_366152,RMVar_hsa_circ_231465,RMVar_hsa_circ_26142,RMVar_hsa_circ_231470,RMVar_hsa_circ_30309,RMVar_hsa_circ_16948,RMVar_hsa_circ_12111,RMVar_hsa_circ_15857,RMVar_hsa_circ_59397,RMVar_hsa_circ_46709,RMVar_hsa_circ_231476,RMVar_hsa_circ_313972,RMVar_hsa_circ_231479 25857 RMVar_ID_25857 Human_SNP_ID_232637139 A-to-I Human chr5 - 55698885 55698885 55698885 TCCAGGTGGCTGGAGTGCAGTGGCGCAATCATAGCTCACTGTAGCCTCCAAATCCTGGGTTTAAG TCCAGGTGGCTGGAGTGCAGTGGCGCAATCATTGCTCACTGTAGCCTCCAAATCCTGGGTTTAAG T A SLC38A9 Ensembl:ENSG00000177058 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs527676645 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43646,RMVar_hsa_circ_341314,RMVar_hsa_circ_366152,RMVar_hsa_circ_26142,RMVar_hsa_circ_30309,RMVar_hsa_circ_16948,RMVar_hsa_circ_59397,RMVar_hsa_circ_46709,RMVar_hsa_circ_231476,RMVar_hsa_circ_313972,RMVar_hsa_circ_109696,RMVar_hsa_circ_291557,RMVar_hsa_circ_367369,RMVar_hsa_circ_231481,RMVar_hsa_circ_231482 25858 RMVar_ID_25858 Human_SNP_ID_232699933 A-to-I Human chr5 - 55961041 55961041 55961041 AAATAGTTTCAAGAGGCTGAGGCAATAGAATCACTTGAACCTGGGAGGCGGAGGTTGCAGTGAGC AAATAGTTTCAAGAGGCTGAGGCAATAGAATCCCTTGAACCTGGGAGGCGGAGGTTGCAGTGAGC T G IL6ST Ensembl:ENSG00000134352 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs540640032 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98956,RMVar_hsa_circ_64552,RMVar_hsa_circ_231485,RMVar_hsa_circ_369180,RMVar_hsa_circ_361365,RMVar_hsa_circ_231488,RMVar_hsa_circ_60420,RMVar_hsa_circ_91721,RMVar_hsa_circ_367460,RMVar_hsa_circ_350729,RMVar_hsa_circ_364699,RMVar_hsa_circ_231491,RMVar_hsa_circ_373570,RMVar_hsa_circ_270540,RMVar_hsa_circ_231493,RMVar_hsa_circ_349891,RMVar_hsa_circ_350378,RMVar_hsa_circ_369181,RMVar_hsa_circ_231495,RMVar_hsa_circ_351797,RMVar_hsa_circ_53250,RMVar_hsa_circ_355117,RMVar_hsa_circ_72918,RMVar_hsa_circ_337035,RMVar_hsa_circ_69819 25859 RMVar_ID_25859 Human_SNP_ID_232736639 A-to-I Human chr5 - 56100160 56100160 56100160 TGAAAATTAACTGTGGGCCACTCGCTGCAGAAATGTAGATGAATATGTATTTTCAACTCTCAAAG TGAAAATTAACTGTGGGCCACTCGCTGCAGAAGTGTAGATGAATATGTATTTTCAACTCTCAAAG T C ANKRD55 Ensembl:ENSG00000164512 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs548463033 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 25860 RMVar_ID_25860 Human_SNP_ID_232751195 A-to-I Human chr5 + 56156028 56156028 56156028 AACCTCAGGGGAAAAGAGGGTTGCACTGTTAGAAACTTCTGCTTTAAAAATGAGAACCAGAGATG AACCTCAGGGGAAAAGAGGGTTGCACTGTTAGCAACTTCTGCTTTAAAAATGAGAACCAGAGATG A C RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs13176226 Functional Loss SNV dbSNP153 33..33 33 - - - 25861 RMVar_ID_25861 Human_SNP_ID_232836582 A-to-I Human chr5 - 56504899 56504899 56504899 CCCATCCGAAAGGATGATGAAGTTCAGGTTGTACGTGGACACTATAAAGGTCAGCAAATTGGCAA CCCATCCGAAAGGATGATGAAGTTCAGGTTGTGCGTGGACACTATAAAGGTCAGCAAATTGGCAA T C RPL26P19 Ensembl:ENSG00000226221 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1482336894 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_284176,Human_RBP_ID_643619,Human_RBP_ID_1041834,Human_RBP_ID_1141498,Human_RBP_ID_1655504,Human_RBP_ID_1996539,Human_RBP_ID_3772670,Human_RBP_ID_7448497,Human_RBP_ID_8617671,Human_RBP_ID_8894353,Human_RBP_ID_9177921,Human_RBP_ID_15464588,Human_RBP_ID_17300646,Human_RBP_ID_17413998,Human_RBP_ID_17532556,Human_RBP_ID_17667916,Human_RBP_ID_18359546,Human_RBP_ID_18538339,Human_RBP_ID_18844061,Human_RBP_ID_24109155,Human_RBP_ID_26531105,Human_RBP_ID_27082682,Human_RBP_ID_27741594 25862 RMVar_ID_25862 Human_SNP_ID_232937767 A-to-I Human chr5 - 56927184 56927184 56927184 TCATGTTGTACATTCCATTGATTTTGGCAAATATATAATGATACATATCCACCAGTACAGTATCA TCATGTTGTACATTCCATTGATTTTGGCAAATGTATAATGATACATATCCACCAGTACAGTATCA T C MIER3 Ensembl:ENSG00000155545 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1044795521 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39620 25863 RMVar_ID_25863 Human_SNP_ID_232937778 A-to-I Human chr5 + 56927229 56927229 56927229 CAATGGAATGTACAACATGAAGAGCGAACCTTAATGTAAACTATGGACTTTAATTAATAATAATG CAATGGAATGTACAACATGAAGAGCGAACCTTCATGTAAACTATGGACTTTAATTAATAATAATG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992636376 Functional Loss SNV dbSNP153 33..33 33 - - - 25864 RMVar_ID_25864 Human_SNP_ID_232937948 A-to-I Human chr5 - 56927985 56927985 56927985 CCTAAATGCATATTATTAAGTGAAGGAAGCCAATCTGAAAAGACTCTATACTGTAGCTTTCCAAA CCTAAATGCATATTATTAAGTGAAGGAAGCCAGTCTGAAAAGACTCTATACTGTAGCTTTCCAAA T C MIER3 Ensembl:ENSG00000155545 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1163478964 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39620 25865 RMVar_ID_25865 Human_SNP_ID_232937949 A-to-I Human chr5 - 56927990 56927990 56927990 GAAATCCTAAATGCATATTATTAAGTGAAGGAAGCCAATCTGAAAAGACTCTATACTGTAGCTTT GAAATCCTAAATGCATATTATTAAGTGAAGGAGGCCAATCTGAAAAGACTCTATACTGTAGCTTT T C MIER3 Ensembl:ENSG00000155545 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202506338 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39620 25866 RMVar_ID_25866 Human_SNP_ID_232937951 A-to-I Human chr5 - 56928000 56928000 56928000 GGAGACATGTGAAATCCTAAATGCATATTATTAAGTGAAGGAAGCCAATCTGAAAAGACTCTATA GGAGACATGTGAAATCCTAAATGCATATTATTGAGTGAAGGAAGCCAATCTGAAAAGACTCTATA T C MIER3 Ensembl:ENSG00000155545 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs557854166 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39620 25867 RMVar_ID_25867 Human_SNP_ID_232937953 A-to-I Human chr5 - 56928003 56928003 56928003 CAAGGAGACATGTGAAATCCTAAATGCATATTATTAAGTGAAGGAAGCCAATCTGAAAAGACTCT CAAGGAGACATGTGAAATCCTAAATGCATATTGTTAAGTGAAGGAAGCCAATCTGAAAAGACTCT T C MIER3 Ensembl:ENSG00000155545 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1300388039 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39620 25868 RMVar_ID_25868 Human_SNP_ID_232942086 A-to-I Human chr5 - 56944963 56944963 56944963 GCTGGGGGCAGTGGCTCAGACATGTAATCTCAACACTTTGGGAGGCTGAAGTGGGATGATCGCTT GCTGGGGGCAGTGGCTCAGACATGTAATCTCAGCACTTTGGGAGGCTGAAGTGGGATGATCGCTT T C MIER3 Ensembl:ENSG00000155545 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928557081 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_231527,RMVar_hsa_circ_231526,RMVar_hsa_circ_362642,RMVar_hsa_circ_329338,RMVar_hsa_circ_87425,RMVar_hsa_circ_266374,RMVar_hsa_circ_331736,RMVar_hsa_circ_231528 25869 RMVar_ID_25869 Human_SNP_ID_233003294 A-to-I Human chr5 + 57183851 57183851 57183851 TGGAGGGCAGTGGTGCCATCACAGTTTGCTGCAGCCTCGACCTCCCAGACACAGGTGATCCTTTC TGGAGGGCAGTGGTGCCATCACAGTTTGCTGCTGCCTCGACCTCCCAGACACAGGTGATCCTTTC A T GPBP1 Ensembl:ENSG00000062194 Protein coding intron GSE38233;GSE100210;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,cerebellum - 24183664,29129909,30559470 RNA-Seq:(High) rs933067796 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15465806 RMVar_hsa_circ_231529,RMVar_hsa_circ_109415 25870 RMVar_ID_25870 Human_SNP_ID_233003308 A-to-I Human chr5 + 57183901 57183901 57183901 ACAGGTGATCCTTTCTTTCACATCAGCCTTCTAAGTAGCTGGGACCACAGGTGAGTGCTGCCATG ACAGGTGATCCTTTCTTTCACATCAGCCTTCTGAGTAGCTGGGACCACAGGTGAGTGCTGCCATG A G GPBP1 Ensembl:ENSG00000062194 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1448004470 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_231529,RMVar_hsa_circ_109415 25871 RMVar_ID_25871 Human_SNP_ID_233004814 A-to-I Human chr5 + 57189046 57189046 57189046 CGAAGTTTCACTCTTGTTGCCTAGGCTGGAGTATAGTGGTGTGATCTTGGCTCACTGCAACCTCT CGAAGTTTCACTCTTGTTGCCTAGGCTGGAGTGTAGTGGTGTGATCTTGGCTCACTGCAACCTCT A G GPBP1 Ensembl:ENSG00000062194 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs377723557 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_231529,RMVar_hsa_circ_109415 25872 RMVar_ID_25872 Human_SNP_ID_233013969 A-to-I Human chr5 + 57220560 57220560 57220560 CTGCTCACTGTAACCTCTGCCCCCCAGGTTCAAACGATTCTCCTGCCTCAGCCTCCTGAGTAGTT CTGCTCACTGTAACCTCTGCCCCCCAGGTTCACACGATTCTCCTGCCTCAGCCTCCTGAGTAGTT A C GPBP1 Ensembl:ENSG00000062194 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1455030270 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81602,RMVar_hsa_circ_231531,RMVar_hsa_circ_231529,RMVar_hsa_circ_109415,RMVar_hsa_circ_274711,RMVar_hsa_circ_341739,RMVar_hsa_circ_370101,RMVar_hsa_circ_376377,RMVar_hsa_circ_267713,RMVar_hsa_circ_31107,RMVar_hsa_circ_75497,RMVar_hsa_circ_231534,RMVar_hsa_circ_231536,RMVar_hsa_circ_231537,RMVar_hsa_circ_231535,RMVar_hsa_circ_231533 25873 RMVar_ID_25873 Human_SNP_ID_233013989 A-to-I Human chr5 + 57220621 57220621 57220621 AGTTGGGATTACAGGTTCCTGCTATCACACCCAGCTGATTTTTGTATTTTTAGTAGAGATGGGGT AGTTGGGATTACAGGTTCCTGCTATCACACCCCGCTGATTTTTGTATTTTTAGTAGAGATGGGGT A C GPBP1 Ensembl:ENSG00000062194 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1014801978 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81602,RMVar_hsa_circ_231531,RMVar_hsa_circ_231529,RMVar_hsa_circ_109415,RMVar_hsa_circ_274711,RMVar_hsa_circ_341739,RMVar_hsa_circ_370101,RMVar_hsa_circ_376377,RMVar_hsa_circ_267713,RMVar_hsa_circ_31107,RMVar_hsa_circ_75497,RMVar_hsa_circ_231534,RMVar_hsa_circ_231536,RMVar_hsa_circ_231537,RMVar_hsa_circ_231535,RMVar_hsa_circ_231533 25874 RMVar_ID_25874 Human_SNP_ID_233013990 A-to-I Human chr5 + 57220621 57220621 57220621 AGTTGGGATTACAGGTTCCTGCTATCACACCCAGCTGATTTTTGTATTTTTAGTAGAGATGGGGT AGTTGGGATTACAGGTTCCTGCTATCACACCCGGCTGATTTTTGTATTTTTAGTAGAGATGGGGT A G GPBP1 Ensembl:ENSG00000062194 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1014801978 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81602,RMVar_hsa_circ_231531,RMVar_hsa_circ_231529,RMVar_hsa_circ_109415,RMVar_hsa_circ_274711,RMVar_hsa_circ_341739,RMVar_hsa_circ_370101,RMVar_hsa_circ_376377,RMVar_hsa_circ_267713,RMVar_hsa_circ_31107,RMVar_hsa_circ_75497,RMVar_hsa_circ_231534,RMVar_hsa_circ_231536,RMVar_hsa_circ_231537,RMVar_hsa_circ_231535,RMVar_hsa_circ_231533 25875 RMVar_ID_25875 Human_SNP_ID_233016890 A-to-I Human chr5 + 57230024 57230024 57230024 GATCTCGGTTCACTGCAACCTCCCCGCCTCCCAGGTTCAAGCGATTCTCTTGCCTCAGCCTCCCG GATCTCGGTTCACTGCAACCTCCCCGCCTCCCGGGTTCAAGCGATTCTCTTGCCTCAGCCTCCCG A G GPBP1 Ensembl:ENSG00000062194 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs188966847 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81602,RMVar_hsa_circ_231531,RMVar_hsa_circ_231529,RMVar_hsa_circ_109415,RMVar_hsa_circ_274711,RMVar_hsa_circ_341739,RMVar_hsa_circ_376377,RMVar_hsa_circ_267713,RMVar_hsa_circ_31107,RMVar_hsa_circ_75497,RMVar_hsa_circ_231534,RMVar_hsa_circ_231536,RMVar_hsa_circ_231537,RMVar_hsa_circ_231535 25876 RMVar_ID_25876 Human_SNP_ID_233019992 A-to-I Human chr5 + 57241506 57241506 57241506 CTAGCACTTTGGGAGGCCGAGGTGGGAAGATCAGTTGAAGCCAAGAGTTTGAGACCAGCCTGGGC CTAGCACTTTGGGAGGCCGAGGTGGGAAGATCTGTTGAAGCCAAGAGTTTGAGACCAGCCTGGGC A T GPBP1 Ensembl:ENSG00000062194 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs897319680 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15467002 RMVar_hsa_circ_5756,RMVar_hsa_circ_81602,RMVar_hsa_circ_231529,RMVar_hsa_circ_109415,RMVar_hsa_circ_341739,RMVar_hsa_circ_267713,RMVar_hsa_circ_75497,RMVar_hsa_circ_231536,RMVar_hsa_circ_231537,RMVar_hsa_circ_351205,RMVar_hsa_circ_73183,RMVar_hsa_circ_62535,RMVar_hsa_circ_308215,RMVar_hsa_circ_363825,RMVar_hsa_circ_339163,RMVar_hsa_circ_274217,RMVar_hsa_circ_231541,RMVar_hsa_circ_231542,RMVar_hsa_circ_231540 25877 RMVar_ID_25877 Human_SNP_ID_233319552 A-to-I Human chr5 - 58454571 58454571 58454571 CTCTTACAAAGATGTAACTGAAAGACTTTTCGAATGGACCCTATGGGACTCCTCTTTTCCACTGT CTCTTACAAAGATGTAACTGAAAGACTTTTCGTATGGACCCTATGGGACTCCTCTTTTCCACTGT T A PLK2 Ensembl:ENSG00000145632 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs547056739 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_312271 RMVar_hsa_circ_123727,RMVar_hsa_circ_231552,RMVar_hsa_circ_121211,RMVar_hsa_circ_231551 25878 RMVar_ID_25878 Human_SNP_ID_233319764 A-to-I Human chr5 - 58455366 58455366 58455366 GCAGAGCTTGGCCAATGCTCAGTTTTCCCAGCAACAGATGCTCCTGAGCAATTTATTAGTCAAGT GCAGAGCTTGGCCAATGCTCAGTTTTCCCAGCGACAGATGCTCCTGAGCAATTTATTAGTCAAGT T C PLK2 Ensembl:ENSG00000145632 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1262967647 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25932476 Human_Splice_Rec_653404,Human_Splice_Rec_653405,Human_Splice_Rec_653438,Human_Splice_Rec_653439,Human_Splice_Rec_653448,Human_Splice_Rec_653449 RMVar_hsa_circ_30401,RMVar_hsa_circ_231552,RMVar_hsa_circ_121211 25879 RMVar_ID_25879 Human_SNP_ID_233448348 A-to-I Human chr5 - 58974094 58974094 58974094 TGCACTGACCTCTACATTTTGTATGATATGTAAAACAGATTTTTTGTAGAGCTTACTTTTATTAT TGCACTGACCTCTACATTTTGTATGATATGTAGAACAGATTTTTTGTAGAGCTTACTTTTATTAT T C PDE4D Ensembl:ENSG00000113448 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs897507155 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1996751,Human_RBP_ID_21088801 RMVar_hsa_circ_231567 25880 RMVar_ID_25880 Human_SNP_ID_233448349 A-to-I Human chr5 - 58974095 58974095 58974095 CTGCACTGACCTCTACATTTTGTATGATATGTAAAACAGATTTTTTGTAGAGCTTACTTTTATTA CTGCACTGACCTCTACATTTTGTATGATATGTGAAACAGATTTTTTGTAGAGCTTACTTTTATTA T C PDE4D Ensembl:ENSG00000113448 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1386209419 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1996751,Human_RBP_ID_21088801 RMVar_hsa_circ_231567 25881 RMVar_ID_25881 Human_SNP_ID_233492488 A-to-I Human chr5 - 59162723 59162723 59162723 ATCCTCCTGTCTACCTGGGACTACAGGCACATAGCACTGCACCACCATACCTGGCTAATTTTTAA ATCCTCCTGTCTACCTGGGACTACAGGCACATCGCACTGCACCACCATACCTGGCTAATTTTTAA T G PDE4D Ensembl:ENSG00000113448 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1188462864 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,RMVar_hsa_circ_335160 25882 RMVar_ID_25882 Human_SNP_ID_233492572 A-to-I Human chr5 - 59162974 59162971 59162975 ATGCCACTGTACTCCAACCTGGGTGACAGAGCAAGACTCTGCCTCGAAGAAAAAAAAAAAATCAA ATGCCACTGTACTCCAACCTGGGTGACAGAG____ACTCTGCCTCGAAGAAAAAAAAAAAATCAA TCTTG T PDE4D Ensembl:ENSG00000113448 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1218549255 Functional Loss DEL dbSNP153 32..35 33 - - - RMVar_hsa_circ_324536,RMVar_hsa_circ_7785,RMVar_hsa_circ_324797,RMVar_hsa_circ_32204,RMVar_hsa_circ_297202,RMVar_hsa_circ_335160 25883 RMVar_ID_25883 Human_SNP_ID_233492574 A-to-I Human chr5 - 59162974 59162974 59162974 ATGCCACTGTACTCCAACCTGGGTGACAGAGCAAGACTCTGCCTCGAAGAAAAAAAAAAAATCAA ATGCCACTGTACTCCAACCTGGGTGACAGAGCCAGACTCTGCCTCGAAGAAAAAAAAAAAATCAA T G PDE4D Ensembl:ENSG00000113448 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1343607773 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,RMVar_hsa_circ_335160 25884 RMVar_ID_25884 Human_SNP_ID_233492753 A-to-I Human chr5 - 59163566 59163566 59163566 GATTTGTACGATAGATTGTTCATTTAAGGACCAGGAGCGGTGGCTCACGCCTGTTATCCAGCATT GATTTGTACGATAGATTGTTCATTTAAGGACCGGGAGCGGTGGCTCACGCCTGTTATCCAGCATT T C PDE4D Ensembl:ENSG00000113448 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 29129909,30559470 RNA-Seq:(High) rs1320923030 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2937828,Human_RBP_ID_25942336 RMVar_hsa_circ_324536,RMVar_hsa_circ_7785,RMVar_hsa_circ_324797,RMVar_hsa_circ_32204,RMVar_hsa_circ_297202,RMVar_hsa_circ_335160 25885 RMVar_ID_25885 Human_SNP_ID_233495087 A-to-I Human chr5 - 59172473 59172473 59172473 CCAGGCTGATCTGGAACTCCTAGGCTCAAGCAATCTGCCCACCTTGGCCTCCCAAAGTGCTGGGA CCAGGCTGATCTGGAACTCCTAGGCTCAAGCAGTCTGCCCACCTTGGCCTCCCAAAGTGCTGGGA T C PDE4D Ensembl:ENSG00000113448 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1224367171 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15470277 RMVar_hsa_circ_324536,RMVar_hsa_circ_330021,RMVar_hsa_circ_7785,RMVar_hsa_circ_324797,RMVar_hsa_circ_32204,RMVar_hsa_circ_297202,RMVar_hsa_circ_335160 25886 RMVar_ID_25886 Human_SNP_ID_233495121 A-to-I Human chr5 - 59172621 59172621 59172621 TCATTGCAACCTCCGCCTCCCAGTCTCCAGCAATCCTCCCACCTCAGCCTCCTGAGTAGCTGGGA TCATTGCAACCTCCGCCTCCCAGTCTCCAGCAGTCCTCCCACCTCAGCCTCCTGAGTAGCTGGGA T C PDE4D Ensembl:ENSG00000113448 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910685115 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_324536,RMVar_hsa_circ_330021,RMVar_hsa_circ_7785,RMVar_hsa_circ_324797,RMVar_hsa_circ_32204,RMVar_hsa_circ_297202,RMVar_hsa_circ_335160 25887 RMVar_ID_25887 Human_SNP_ID_233556129 A-to-I Human chr5 - 59423203 59423203 59423203 GGATGATGAGGCCTGAGGATGAGTAACAACATACTCTGCTGAGAACCACATGAATGAAGCCCTGA GGATGATGAGGCCTGAGGATGAGTAACAACATGCTCTGCTGAGAACCACATGAATGAAGCCCTGA T C PDE4D Ensembl:ENSG00000113448 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1360466888 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25249,RMVar_hsa_circ_7785,RMVar_hsa_circ_26973,RMVar_hsa_circ_231584,RMVar_hsa_circ_231590,RMVar_hsa_circ_231585,RMVar_hsa_circ_231587,RMVar_hsa_circ_231586 25888 RMVar_ID_25888 Human_SNP_ID_233556147 A-to-I Human chr5 - 59423312 59423312 59423312 AAATATGTGATTACAATTGTGAGAACTGCTCAAAAGGAAACAAGGACCCAGTGAGAGTATAAAAA AAATATGTGATTACAATTGTGAGAACTGCTCAGAAGGAAACAAGGACCCAGTGAGAGTATAAAAA T C PDE4D Ensembl:ENSG00000113448 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs529544877 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25249,RMVar_hsa_circ_7785,RMVar_hsa_circ_26973,RMVar_hsa_circ_231584,RMVar_hsa_circ_231590,RMVar_hsa_circ_231585,RMVar_hsa_circ_231587,RMVar_hsa_circ_231586 25889 RMVar_ID_25889 Human_SNP_ID_233586272 A-to-I Human chr5 - 59552095 59552094 59552095 TCTGCTTCAGCCTCTTGAGTAGCTAGGTCTACAGACATCCACCACCACCCCTGGACAGTTTTTCA TCTGCTTCAGCCTCTTGAGTAGCTAGGTCTAC_GACATCCACCACCACCCCTGGACAGTTTTTCA CT C PDE4D Ensembl:ENSG00000113448 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1252037024 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_25249,RMVar_hsa_circ_231594,RMVar_hsa_circ_231595,RMVar_hsa_circ_231598,RMVar_hsa_circ_231597 25890 RMVar_ID_25890 Human_SNP_ID_233586289 A-to-I Human chr5 - 59552183 59552183 59552183 ACTTACTTTCTTACTGTTGTCCAGGCTGGAGTACAATGGCACAATCTCAGCTCACTGCAACCTTC ACTTACTTTCTTACTGTTGTCCAGGCTGGAGTTCAATGGCACAATCTCAGCTCACTGCAACCTTC T A PDE4D Ensembl:ENSG00000113448 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1055926228 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25249,RMVar_hsa_circ_231594,RMVar_hsa_circ_231595,RMVar_hsa_circ_231598,RMVar_hsa_circ_231597 25891 RMVar_ID_25891 Human_SNP_ID_233591031 A-to-I Human chr5 - 59572655 59572655 59572655 TAATATGGTGAAGCCCCGTCTCTACTAAAAATACAAAAAATTAGCTGGGCGTGGTGGCGGGCGCC TAATATGGTGAAGCCCCGTCTCTACTAAAAATGCAAAAAATTAGCTGGGCGTGGTGGCGGGCGCC T C PDE4D Ensembl:ENSG00000113448 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1459484043 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25904197 RMVar_hsa_circ_25249 25892 RMVar_ID_25892 Human_SNP_ID_233610743 A-to-I Human chr5 - 59654081 59654081 59654081 ACACCTCAGCCTCCAGAGTAGCTGGGAATACAAGTGCATGGCACCATGCCTGGCTAATTTTTACA ACACCTCAGCCTCCAGAGTAGCTGGGAATACACGTGCATGGCACCATGCCTGGCTAATTTTTACA T G PDE4D Ensembl:ENSG00000113448 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474443451 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25249 25893 RMVar_ID_25893 Human_SNP_ID_233611359 A-to-I Human chr5 - 59656823 59656823 59656823 ATGAATAATAATTATTTGCTATTGTAATTGCTAAAACTGAAGAGTGTCTCAGAAAGTATAATTTA ATGAATAATAATTATTTGCTATTGTAATTGCTGAAACTGAAGAGTGTCTCAGAAAGTATAATTTA T C PDE4D Ensembl:ENSG00000113448 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1561418007 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15473495 RMVar_hsa_circ_25249 25894 RMVar_ID_25894 Human_SNP_ID_233611376 A-to-I Human chr5 - 59656891 59656891 59656891 AAAGTTAAAGACTTCTTGGAAATGCTATCTCTATAAGGAATATGACCATTTGCTATGTTAATACT AAAGTTAAAGACTTCTTGGAAATGCTATCTCTGTAAGGAATATGACCATTTGCTATGTTAATACT T C PDE4D Ensembl:ENSG00000113448 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1200057474 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2939461 RMVar_hsa_circ_25249 25895 RMVar_ID_25895 Human_SNP_ID_233611379 A-to-I Human chr5 - 59656897 59656897 59656897 AGAAAAAAAGTTAAAGACTTCTTGGAAATGCTATCTCTATAAGGAATATGACCATTTGCTATGTT AGAAAAAAAGTTAAAGACTTCTTGGAAATGCTGTCTCTATAAGGAATATGACCATTTGCTATGTT T C PDE4D Ensembl:ENSG00000113448 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1264792454 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2939461 RMVar_hsa_circ_25249 25896 RMVar_ID_25896 Human_SNP_ID_233611380 A-to-I Human chr5 - 59656897 59656897 59656897 AGAAAAAAAGTTAAAGACTTCTTGGAAATGCTATCTCTATAAGGAATATGACCATTTGCTATGTT AGAAAAAAAGTTAAAGACTTCTTGGAAATGCTCTCTCTATAAGGAATATGACCATTTGCTATGTT T G PDE4D Ensembl:ENSG00000113448 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1264792454 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2939461 RMVar_hsa_circ_25249 25897 RMVar_ID_25897 Human_SNP_ID_233611382 A-to-I Human chr5 - 59656916 59656914 59656916 GAGACTGAAATGACAAATTAGAAAAAAAGTTAAAGACTTCTTGGAAATGCTATCTCTATAAGGAA GAGACTGAAATGACAAATTAGAAAAAAAGTTA__GACTTCTTGGAAATGCTATCTCTATAAGGAA CTT C PDE4D Ensembl:ENSG00000113448 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1040445369 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_26704007 RMVar_hsa_circ_25249 25898 RMVar_ID_25898 Human_SNP_ID_233611389 A-to-I Human chr5 - 59656926 59656926 59656926 TGTTTTCTGAGAGACTGAAATGACAAATTAGAAAAAAAGTTAAAGACTTCTTGGAAATGCTATCT TGTTTTCTGAGAGACTGAAATGACAAATTAGAGAAAAAGTTAAAGACTTCTTGGAAATGCTATCT T C PDE4D Ensembl:ENSG00000113448 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs189525290 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25249 25899 RMVar_ID_25899 Human_SNP_ID_233611729 A-to-I Human chr5 - 59658493 59658493 59658493 CCTGCAGTCCCAGCTACTCCAGAGGCTGAGGCAGGAGAATGGCGTGAACCCAGAAGGCAGAGCTT CCTGCAGTCCCAGCTACTCCAGAGGCTGAGGCTGGAGAATGGCGTGAACCCAGAAGGCAGAGCTT T A PDE4D Ensembl:ENSG00000113448 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886092409 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25249 25900 RMVar_ID_25900 Human_SNP_ID_233611730 A-to-I Human chr5 - 59658493 59658493 59658493 CCTGCAGTCCCAGCTACTCCAGAGGCTGAGGCAGGAGAATGGCGTGAACCCAGAAGGCAGAGCTT CCTGCAGTCCCAGCTACTCCAGAGGCTGAGGCCGGAGAATGGCGTGAACCCAGAAGGCAGAGCTT T G PDE4D Ensembl:ENSG00000113448 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886092409 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25249 25901 RMVar_ID_25901 Human_SNP_ID_233613936 A-to-I Human chr5 - 59668698 59668698 59668698 TCTTCTTCTTTTTTTTCTTGAGGCAGGGTCTCACTCTGGACTCTGTCCAGGCTGGAGTGCAGTGG TCTTCTTCTTTTTTTTCTTGAGGCAGGGTCTCCCTCTGGACTCTGTCCAGGCTGGAGTGCAGTGG T G PDE4D Ensembl:ENSG00000113448 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1028528404 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15473651,Human_RBP_ID_21214405 RMVar_hsa_circ_25249 25902 RMVar_ID_25902 Human_SNP_ID_233629939 A-to-I Human chr5 - 59735915 59735915 59735915 CCTGTAATCCTAGAACTTTGGGAGGCCGAGGCAGATGGATCATTTGAGACGAGGAGTTCAAGATC CCTGTAATCCTAGAACTTTGGGAGGCCGAGGCCGATGGATCATTTGAGACGAGGAGTTCAAGATC T G PDE4D Ensembl:ENSG00000113448 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1299039739 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25249 25903 RMVar_ID_25903 Human_SNP_ID_158140233 A-to-I Human chr3 + 150451893 150451893 150451893 TGAAAAAGAGAAGTAGTTCTCTTATTTTTTTTAGAGACAGATCTGGCTCTGTCACCCAGGCTGGA TGAAAAAGAGAAGTAGTTCTCTTATTTTTTTTGGAGACAGATCTGGCTCTGTCACCCAGGCTGGA A G TSC22D2 Ensembl:ENSG00000196428 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1298662383 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7136445,Human_RBP_ID_10071500,Human_RBP_ID_14669437 25904 RMVar_ID_25904 Human_SNP_ID_158140259 A-to-I Human chr3 + 150451990 150451990 150451990 AGCAGTCTTCCCACACAGCCTCCTGAGTAACTAGGACCGTGGGCTTGCTTTCTTTTCTCTTTTCT AGCAGTCTTCCCACACAGCCTCCTGAGTAACTGGGACCGTGGGCTTGCTTTCTTTTCTCTTTTCT A G TSC22D2 Ensembl:ENSG00000196428 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1470089145 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7136447 25905 RMVar_ID_25905 Human_SNP_ID_158167545 A-to-I Human chr3 - 150571008 150571008 150571008 GGTCTGGAGTTTAGTGGCACGGTCTCGGCTCAATGCAACCTCTGCCTCCCAGGTTCAAACAAGTC GGTCTGGAGTTTAGTGGCACGGTCTCGGCTCAGTGCAACCTCTGCCTCCCAGGTTCAAACAAGTC T C SERP1 Ensembl:ENSG00000120742 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs550530828 Functional Loss SNV dbSNP153 33..33 33 - - - 25906 RMVar_ID_25906 Human_SNP_ID_158167551 A-to-I Human chr3 + 150571029 150571029 150571029 CAGAGGTTGCATTGAGCCGAGACCGTGCCACTAAACTCCAGACCGGGCAACAAGAGTGAAACTCC CAGAGGTTGCATTGAGCCGAGACCGTGCCACTGAACTCCAGACCGGGCAACAAGAGTGAAACTCC A G EIF2A Ensembl:ENSG00000144895 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs898454522 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_354495,RMVar_hsa_circ_341732,RMVar_hsa_circ_378355,RMVar_hsa_circ_340785,RMVar_hsa_circ_222170,RMVar_hsa_circ_16788,RMVar_hsa_circ_300916,RMVar_hsa_circ_222174,RMVar_hsa_circ_361416,RMVar_hsa_circ_335268 25907 RMVar_ID_25907 Human_SNP_ID_158173195 A-to-I Human chr3 - 150594847 150594847 150594847 TTAAAAAAAGTACCAAATAGGCCAGGAGCGGTAGCTCATGCCTGTAATCCCAGCGCTTTGGGATA TTAAAAAAAGTACCAAATAGGCCAGGAGCGGTTGCTCATGCCTGTAATCCCAGCGCTTTGGGATA T A SERP1 Ensembl:ENSG00000120742 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs751966060 Functional Loss SNV dbSNP153 33..33 33 - - - 25908 RMVar_ID_25908 Human_SNP_ID_158174974 A-to-I Human chr3 - 150602654 150602654 150602654 ATCTGTATATATATATTTTTAAACACGGTCTCACTGTCACCCAGGCTGGAGTTCAGTGGCGTGAT ATCTGTATATATATATTTTTAAACACGGTCTCGCTGTCACCCAGGCTGGAGTTCAGTGGCGTGAT T C SERP1 Ensembl:ENSG00000120742 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1231159714 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3691004,Human_RBP_ID_8561937 25909 RMVar_ID_25909 Human_SNP_ID_158178306 A-to-I Human chr3 + 150616780 150616780 150616780 ATTTGAATGTCTACTTTCAAGTAGCTGGGACTACAGGTGCATGCCACCATGCCCAGCTAATTTTT ATTTGAATGTCTACTTTCAAGTAGCTGGGACTGCAGGTGCATGCCACCATGCCCAGCTAATTTTT A G SELENOT Ensembl:ENSG00000198843 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1157094279 Functional Loss SNV dbSNP153 33..33 33 - - - 25910 RMVar_ID_25910 Human_SNP_ID_158202851 A-to-I Human chr3 + 150718904 150718904 150718904 GCTGATGTTGGGAGTTCGAGACCAGTCTGACTAACATGGAGAAACCCCGTCTCTACTAAAAATAC GCTGATGTTGGGAGTTCGAGACCAGTCTGACTCACATGGAGAAACCCCGTCTCTACTAAAAATAC A C ERICH6-AS1 Ensembl:ENSG00000240137 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1408510045 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_222182 25911 RMVar_ID_25911 Human_SNP_ID_158208066 A-to-I Human chr3 - 150741361 150741361 150741361 TTTTGGGTGGATTGCCTAGGAAAGCAAGTCATATGGCCATTGATAGTTCTCATGTAATTAGTTTT TTTTGGGTGGATTGCCTAGGAAAGCAAGTCATGTGGCCATTGATAGTTCTCATGTAATTAGTTTT T C SIAH2 Ensembl:ENSG00000181788 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1254462269 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_592687,Human_RBP_ID_8561986 Human_miRNA_ID_878880,Human_miRNA_ID_2072129,Human_miRNA_ID_2073811,Human_miRNA_ID_2392537,Human_miRNA_ID_3063969 RMVar_hsa_circ_75835,RMVar_hsa_circ_92856,RMVar_hsa_circ_222183,RMVar_hsa_circ_222184 25912 RMVar_ID_25912 Human_SNP_ID_158239147 A-to-I Human chr3 + 150871703 150871703 150871703 AAACCCTGTCTCTACTAAAAATACAGAAAATTAGCTGTGTGTGGTGGCGCGCGCCTGTAATCCCA AAACCCTGTCTCTACTAAAAATACAGAAAATTGGCTGTGTGTGGTGGCGCGCGCCTGTAATCCCA A G CLRN1-AS1,SIAH2-AS1 Ensembl:ENSG00000239265,Ensembl:ENSG00000244265 lincRNA,lincRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1314777682 Functional Loss SNV dbSNP153 33..33 33 - - - 25913 RMVar_ID_25913 Human_SNP_ID_158593454 A-to-I Human chr3 + 152330240 152330240 152330240 GGGTTCAAGCGATCCTTCTGCCTTACTTTCCCAAGTATCTGGGACTACAGATGCACACCACTGCC GGGTTCAAGCGATCCTTCTGCCTTACTTTCCCGAGTATCTGGGACTACAGATGCACACCACTGCC A G MBNL1 Ensembl:ENSG00000152601 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1034863652 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_220,RMVar_hsa_circ_88218,RMVar_hsa_circ_342970,RMVar_hsa_circ_8585,RMVar_hsa_circ_222204 25914 RMVar_ID_25914 Human_SNP_ID_158621252 A-to-I Human chr3 + 152448640 152448640 152448640 GAGACTTACTTAATAAAATTATTTTATTAATTAAATTAATGAGTAGATATATATGTCAAAAATCC GAGACTTACTTAATAAAATTATTTTATTAATTTAATTAATGAGTAGATATATATGTCAAAAATCC A T MBNL1 Ensembl:ENSG00000152601 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs991786380 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88218,RMVar_hsa_circ_57391,RMVar_hsa_circ_222204,RMVar_hsa_circ_349168,RMVar_hsa_circ_11312,RMVar_hsa_circ_105430,RMVar_hsa_circ_222209 25915 RMVar_ID_25915 Human_SNP_ID_159071710 A-to-I Human chr3 - 154284659 154284658 154284660 GGCTATGTCTGCTATTTTTAAGGGAAAAGAAAAGATTGCAGATGCAAGAAGAAAGGAATTGGCAA GGCTATGTCTGCTATTTTTAAGGGAAAAGAA__GATTGCAGATGCAAGAAGAAAGGAATTGGCAA CTT C DHX36 Ensembl:ENSG00000174953 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs746732662 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_282467,Human_RBP_ID_1953057,Human_RBP_ID_3964306,Human_RBP_ID_23978600 Human_Splice_Rec_497386,Human_Splice_Rec_497387,Human_Splice_Rec_497484,Human_Splice_Rec_497485,Human_Splice_Rec_497500,Human_Splice_Rec_497501,Human_Splice_Rec_497542,Human_Splice_Rec_497543,Human_Splice_Rec_497564 RMVar_hsa_circ_45294,RMVar_hsa_circ_103393,RMVar_hsa_circ_222231,RMVar_hsa_circ_60815,RMVar_hsa_circ_32214,RMVar_hsa_circ_112228,RMVar_hsa_circ_222232,RMVar_hsa_circ_222234,RMVar_hsa_circ_222233,RMVar_hsa_circ_44876,RMVar_hsa_circ_222238,RMVar_hsa_circ_286689,RMVar_hsa_circ_23455,RMVar_hsa_circ_51817,RMVar_hsa_circ_330036,RMVar_hsa_circ_222239,RMVar_hsa_circ_337366,RMVar_hsa_circ_300280,RMVar_hsa_circ_125134,RMVar_hsa_circ_271215,RMVar_hsa_circ_72662,RMVar_hsa_circ_222240,RMVar_hsa_circ_222242,RMVar_hsa_circ_222244,RMVar_hsa_circ_222245,RMVar_hsa_circ_222246,RMVar_hsa_circ_222243,RMVar_hsa_circ_222241 25916 RMVar_ID_25916 Human_SNP_ID_159429156 A-to-I Human chr3 - 155761662 155761662 155761662 CACTGCAACCTCTCCCTTCCCAGATTCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGA CACTGCAACCTCTCCCTTCCCAGATTCAAGCAGTTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1008533716 Functional Loss SNV dbSNP153 33..33 33 - - - 25917 RMVar_ID_25917 Human_SNP_ID_159444525 A-to-I Human chr3 - 155821929 155821929 155821929 GTCTCTACTGCAAATACAGAAATTAGCCGGGCATGGTGGTGGGCACCTGTAATCCCAGCTACTTG GTCTCTACTGCAAATACAGAAATTAGCCGGGCGTGGTGGTGGGCACCTGTAATCCCAGCTACTTG T C SLC33A1,AC104472.3 Ensembl:ENSG00000169359,Ensembl:ENSG00000284952 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1207831911 Functional Loss SNV dbSNP153 33..33 33 - - - 25918 RMVar_ID_25918 Human_SNP_ID_159444528 A-to-I Human chr3 - 155821937 155821937 155821937 GAAACCCTGTCTCTACTGCAAATACAGAAATTAGCCGGGCATGGTGGTGGGCACCTGTAATCCCA GAAACCCTGTCTCTACTGCAAATACAGAAATTGGCCGGGCATGGTGGTGGGCACCTGTAATCCCA T C SLC33A1,AC104472.3 Ensembl:ENSG00000169359,Ensembl:ENSG00000284952 Protein coding,Protein coding 3'UTR,intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1327289968 Functional Loss SNV dbSNP153 33..33 33 - - - 25919 RMVar_ID_25919 Human_SNP_ID_159444757 A-to-I Human chr3 - 155822966 155822966 155822966 GCTGGGTGTAGTGGCTCATACCTTTAATCCCAACACTTTGGGATGCCAAGGTAGGAGTATTGCTT GCTGGGTGTAGTGGCTCATACCTTTAATCCCAGCACTTTGGGATGCCAAGGTAGGAGTATTGCTT T C SLC33A1,AC104472.3 Ensembl:ENSG00000169359,Ensembl:ENSG00000284952 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1304638964 Functional Loss SNV dbSNP153 33..33 33 - - - 25920 RMVar_ID_25920 Human_SNP_ID_159444842 A-to-I Human chr3 - 155823413 155823413 155823413 TTCCCGCCTTGGCCTCCTAAAGTGCTGGGATTACAGGCGTGAGCCACCGCTGCTGGCTCTTTTTA TTCCCGCCTTGGCCTCCTAAAGTGCTGGGATTCCAGGCGTGAGCCACCGCTGCTGGCTCTTTTTA T G SLC33A1,AC104472.3 Ensembl:ENSG00000169359,Ensembl:ENSG00000284952 Protein coding,Protein coding 3'UTR,intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1448694337 Functional Loss SNV dbSNP153 33..33 33 - - - 25921 RMVar_ID_25921 Human_SNP_ID_159445184 A-to-I Human chr3 - 155824991 155824991 155824991 CTTCAAGCAGTCGTCCAGCCTTGACCTCTCAAAATGCTGGGATTACAGGTGTAAGCCACCGTGCC CTTCAAGCAGTCGTCCAGCCTTGACCTCTCAATATGCTGGGATTACAGGTGTAAGCCACCGTGCC T A SLC33A1,AC104472.3 Ensembl:ENSG00000169359,Ensembl:ENSG00000284952 Protein coding,Protein coding 3'UTR,intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs948677146 Functional Loss SNV dbSNP153 33..33 33 - - - 25922 RMVar_ID_25922 Human_SNP_ID_159445194 A-to-I Human chr3 - 155825025 155825024 155825026 CGCTATATTTTCCAGGCTAGTCCCAATCTCATAGCTTCAAGCAGTCGTCCAGCCTTGACCTCTCA CGCTATATTTTCCAGGCTAGTCCCAATCTCA__GCTTCAAGCAGTCGTCCAGCCTTGACCTCTCA CTA C SLC33A1,AC104472.3 Ensembl:ENSG00000169359,Ensembl:ENSG00000284952 Protein coding,Protein coding 3'UTR,intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs761686405 Functional Loss DEL dbSNP153 32..33 33 - - - 25923 RMVar_ID_25923 Human_SNP_ID_159448406 A-to-I Human chr3 - 155838107 155838107 155838107 TAGGGACAGGGTTTCTCCATGTTTGTCAGGCTAGTCTCGAACTCCCGACCTCAGGTGATCTGCCC TAGGGACAGGGTTTCTCCATGTTTGTCAGGCTGGTCTCGAACTCCCGACCTCAGGTGATCTGCCC T C SLC33A1,AC104472.3 Ensembl:ENSG00000169359,Ensembl:ENSG00000284952 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs972006215 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_281006,RMVar_hsa_circ_222286,RMVar_hsa_circ_297559,RMVar_hsa_circ_222291,RMVar_hsa_circ_222289,RMVar_hsa_circ_271422,RMVar_hsa_circ_222292,RMVar_hsa_circ_44775 25924 RMVar_ID_25924 Human_SNP_ID_159448407 A-to-I Human chr3 - 155838107 155838107 155838107 TAGGGACAGGGTTTCTCCATGTTTGTCAGGCTAGTCTCGAACTCCCGACCTCAGGTGATCTGCCC TAGGGACAGGGTTTCTCCATGTTTGTCAGGCTCGTCTCGAACTCCCGACCTCAGGTGATCTGCCC T G SLC33A1,AC104472.3 Ensembl:ENSG00000169359,Ensembl:ENSG00000284952 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs972006215 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_281006,RMVar_hsa_circ_222286,RMVar_hsa_circ_297559,RMVar_hsa_circ_222291,RMVar_hsa_circ_222289,RMVar_hsa_circ_271422,RMVar_hsa_circ_222292,RMVar_hsa_circ_44775 25925 RMVar_ID_25925 Human_SNP_ID_159450234 A-to-I Human chr3 - 155844747 155844747 155844747 GATGTTATTTTATACTGGGCGTGGTGGCTCACACCCGTGATCCTGGCTCTTTGGGAGGCCAAGGC GATGTTATTTTATACTGGGCGTGGTGGCTCACCCCCGTGATCCTGGCTCTTTGGGAGGCCAAGGC T G SLC33A1,AC104472.3 Ensembl:ENSG00000169359,Ensembl:ENSG00000284952 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6792780 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_222292 25926 RMVar_ID_25926 Human_SNP_ID_159451083 A-to-I Human chr3 - 155848515 155848515 155848515 ACCATGCCCTGCTAATTTTTTGTATTTTTAGTAGAGACAGGGTTGCACCATGTTAGCCAGGATGG ACCATGCCCTGCTAATTTTTTGTATTTTTAGTGGAGACAGGGTTGCACCATGTTAGCCAGGATGG T C SLC33A1,AC104472.3 Ensembl:ENSG00000169359,Ensembl:ENSG00000284952 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs9826557 Functional Loss SNV dbSNP153 33..33 33 - - - 25927 RMVar_ID_25927 Human_SNP_ID_159451098 A-to-I Human chr3 - 155848570 155848570 155848570 TCACACCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCCACCACCATGCCCT TCACACCATTCTCCTGCCTCAGCCTCCCGAGTGGCTGGGACTACAGGCGCCCACCACCATGCCCT T C SLC33A1,AC104472.3 Ensembl:ENSG00000169359,Ensembl:ENSG00000284952 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs939270940 Functional Loss SNV dbSNP153 33..33 33 - - - 25928 RMVar_ID_25928 Human_SNP_ID_159451130 A-to-I Human chr3 - 155848668 155848668 155848668 TTCTTTTTTTGTTGTTGTTGAGACAGAGTCTCACTTTGTTGCCCAGGCTGGAATGCAGTGGTGCG TTCTTTTTTTGTTGTTGTTGAGACAGAGTCTCGCTTTGTTGCCCAGGCTGGAATGCAGTGGTGCG T C SLC33A1,AC104472.3 Ensembl:ENSG00000169359,Ensembl:ENSG00000284952 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1011832978 Functional Loss SNV dbSNP153 33..33 33 - - - 25929 RMVar_ID_25929 Human_SNP_ID_159451220 A-to-I Human chr3 - 155849081 155849081 155849081 GTGAAACCCCAGCTCTACTAAAAATACAAAAAATTAGCCGGGTGTGGTGGCGCATACCTGTGATC GTGAAACCCCAGCTCTACTAAAAATACAAAAAGTTAGCCGGGTGTGGTGGCGCATACCTGTGATC T C SLC33A1,AC104472.3 Ensembl:ENSG00000169359,Ensembl:ENSG00000284952 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs760105181 Functional Loss SNV dbSNP153 33..33 33 - - - 25930 RMVar_ID_25930 Human_SNP_ID_159451489 A-to-I Human chr3 - 155850182 155850174 155850182 CAACATGGTGAAACCTTGTCTCTTCTAAAAATACAAAAATTAGCCCGGTGTGATGGCATGCACCT CAACATGGTGAAACCTTGTCTCTTCTAAAAAT________TAGCCCGGTGTGATGGCATGCACCT AATTTTTGT A SLC33A1,AC104472.3 Ensembl:ENSG00000169359,Ensembl:ENSG00000284952 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1199200985 Functional Loss DEL dbSNP153 33..40 33 - - - 25931 RMVar_ID_25931 Human_SNP_ID_159451605 A-to-I Human chr3 - 155850754 155850754 155850754 AAATTAGGTGGAAGTGGTGGCATTCACTTGTAATCCCAGCTACTCAGGAGGCTGGGTGGGGAGAA AAATTAGGTGGAAGTGGTGGCATTCACTTGTAGTCCCAGCTACTCAGGAGGCTGGGTGGGGAGAA T C SLC33A1,AC104472.3 Ensembl:ENSG00000169359,Ensembl:ENSG00000284952 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1212073649 Functional Loss SNV dbSNP153 33..33 33 - - - 25932 RMVar_ID_25932 Human_SNP_ID_159459734 A-to-I Human chr3 + 155883171 155883171 155883171 TCAGCTCACTGCAGCTTCTGCCTCCTAGGTTCAAGCCATTCTCATGCCTCAGGCTCCCGAGTAAC TCAGCTCACTGCAGCTTCTGCCTCCTAGGTTCCAGCCATTCTCATGCCTCAGGCTCCCGAGTAAC A C GMPS Ensembl:ENSG00000163655 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs999153990 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109356,RMVar_hsa_circ_222294,RMVar_hsa_circ_222295 25933 RMVar_ID_25933 Human_SNP_ID_159466822 A-to-I Human chr3 + 155913683 155913683 155913683 GCTGGGATTGCAGACATGTGCCACTACGCCCCACTAATTTTTGTGTTTTTAGTAGAGATGTGGTT GCTGGGATTGCAGACATGTGCCACTACGCCCCGCTAATTTTTGTGTTTTTAGTAGAGATGTGGTT A G GMPS Ensembl:ENSG00000163655 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1878213 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2550,GWAS_ID_2551,GWAS_ID_2552,GWAS_ID_2553,GWAS_ID_2554,GWAS_ID_2555,GWAS_ID_2556,GWAS_ID_2557,GWAS_ID_2558,GWAS_ID_2559,GWAS_ID_2560,GWAS_ID_2561,GWAS_ID_2562,GWAS_ID_2563,GWAS_ID_2564,GWAS_ID_2565,GWAS_ID_2566,GWAS_ID_2567,GWAS_ID_2568,GWAS_ID_2569,GWAS_ID_2570,GWAS_ID_2571,GWAS_ID_2572,GWAS_ID_2573,GWAS_ID_2574,GWAS_ID_2575,GWAS_ID_2576,GWAS_ID_2577,GWAS_ID_2578,GWAS_ID_2579,GWAS_ID_2580,GWAS_ID_2581,GWAS_ID_2582,GWAS_ID_2583,GWAS_ID_2584 RMVar_hsa_circ_222301,RMVar_hsa_circ_90348,RMVar_hsa_circ_109356,RMVar_hsa_circ_222294,RMVar_hsa_circ_275274,RMVar_hsa_circ_338627,RMVar_hsa_circ_222296,RMVar_hsa_circ_328670,RMVar_hsa_circ_311283,RMVar_hsa_circ_317214,RMVar_hsa_circ_298340,RMVar_hsa_circ_283583,RMVar_hsa_circ_284589,RMVar_hsa_circ_17557,RMVar_hsa_circ_222297,RMVar_hsa_circ_222299,RMVar_hsa_circ_222300,RMVar_hsa_circ_222298,RMVar_hsa_circ_222307,RMVar_hsa_circ_339630,RMVar_hsa_circ_357138,RMVar_hsa_circ_378672,RMVar_hsa_circ_343023,RMVar_hsa_circ_304419,RMVar_hsa_circ_291478,RMVar_hsa_circ_222308,RMVar_hsa_circ_283772,RMVar_hsa_circ_331312,RMVar_hsa_circ_373218,RMVar_hsa_circ_222319,RMVar_hsa_circ_222315,RMVar_hsa_circ_317044,RMVar_hsa_circ_222310,RMVar_hsa_circ_222311,RMVar_hsa_circ_375108,RMVar_hsa_circ_222309,RMVar_hsa_circ_353808,RMVar_hsa_circ_297558,RMVar_hsa_circ_222316,RMVar_hsa_circ_293737,RMVar_hsa_circ_315248,RMVar_hsa_circ_375572,RMVar_hsa_circ_350088,RMVar_hsa_circ_307249,RMVar_hsa_circ_275066,RMVar_hsa_circ_222321,RMVar_hsa_circ_222322,RMVar_hsa_circ_222320,RMVar_hsa_circ_222317,RMVar_hsa_circ_222318 25934 RMVar_ID_25934 Human_SNP_ID_159466823 A-to-I Human chr3 + 155913683 155913683 155913683 GCTGGGATTGCAGACATGTGCCACTACGCCCCACTAATTTTTGTGTTTTTAGTAGAGATGTGGTT GCTGGGATTGCAGACATGTGCCACTACGCCCCTCTAATTTTTGTGTTTTTAGTAGAGATGTGGTT A T GMPS Ensembl:ENSG00000163655 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1878213 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2550,GWAS_ID_2551,GWAS_ID_2552,GWAS_ID_2553,GWAS_ID_2554,GWAS_ID_2555,GWAS_ID_2556,GWAS_ID_2557,GWAS_ID_2558,GWAS_ID_2559,GWAS_ID_2560,GWAS_ID_2561,GWAS_ID_2562,GWAS_ID_2563,GWAS_ID_2564,GWAS_ID_2565,GWAS_ID_2566,GWAS_ID_2567,GWAS_ID_2568,GWAS_ID_2569,GWAS_ID_2570,GWAS_ID_2571,GWAS_ID_2572,GWAS_ID_2573,GWAS_ID_2574,GWAS_ID_2575,GWAS_ID_2576,GWAS_ID_2577,GWAS_ID_2578,GWAS_ID_2579,GWAS_ID_2580,GWAS_ID_2581,GWAS_ID_2582,GWAS_ID_2583,GWAS_ID_2584 RMVar_hsa_circ_222301,RMVar_hsa_circ_90348,RMVar_hsa_circ_109356,RMVar_hsa_circ_222294,RMVar_hsa_circ_275274,RMVar_hsa_circ_338627,RMVar_hsa_circ_222296,RMVar_hsa_circ_328670,RMVar_hsa_circ_311283,RMVar_hsa_circ_317214,RMVar_hsa_circ_298340,RMVar_hsa_circ_283583,RMVar_hsa_circ_284589,RMVar_hsa_circ_17557,RMVar_hsa_circ_222297,RMVar_hsa_circ_222299,RMVar_hsa_circ_222300,RMVar_hsa_circ_222298,RMVar_hsa_circ_222307,RMVar_hsa_circ_339630,RMVar_hsa_circ_357138,RMVar_hsa_circ_378672,RMVar_hsa_circ_343023,RMVar_hsa_circ_304419,RMVar_hsa_circ_291478,RMVar_hsa_circ_222308,RMVar_hsa_circ_283772,RMVar_hsa_circ_331312,RMVar_hsa_circ_373218,RMVar_hsa_circ_222319,RMVar_hsa_circ_222315,RMVar_hsa_circ_317044,RMVar_hsa_circ_222310,RMVar_hsa_circ_222311,RMVar_hsa_circ_375108,RMVar_hsa_circ_222309,RMVar_hsa_circ_353808,RMVar_hsa_circ_297558,RMVar_hsa_circ_222316,RMVar_hsa_circ_293737,RMVar_hsa_circ_315248,RMVar_hsa_circ_375572,RMVar_hsa_circ_350088,RMVar_hsa_circ_307249,RMVar_hsa_circ_275066,RMVar_hsa_circ_222321,RMVar_hsa_circ_222322,RMVar_hsa_circ_222320,RMVar_hsa_circ_222317,RMVar_hsa_circ_222318 25935 RMVar_ID_25935 Human_SNP_ID_159474082 A-to-I Human chr3 + 155943120 155943120 155943120 GGGCTTGGTGGCGCGCGCCTGTAATCCCAGCTACTCGGAAGGCTGAGGTGTGAGAATCACTTAAA GGGCTTGGTGGCGCGCGCCTGTAATCCCAGCTGCTCGGAAGGCTGAGGTGTGAGAATCACTTAAA A G GMPS Ensembl:ENSG00000163655 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1429935438 Functional Loss SNV dbSNP153 33..33 33 - - - 25936 RMVar_ID_25936 Human_SNP_ID_159474098 A-to-I Human chr3 + 155943172 155943172 155943172 AGAATCACTTAAACCCGGGAGATGGAGGTTGCAGTGAGCAGAGATTGCGCCACTGCACTCCAGCC AGAATCACTTAAACCCGGGAGATGGAGGTTGCCGTGAGCAGAGATTGCGCCACTGCACTCCAGCC A C GMPS Ensembl:ENSG00000163655 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1163426584 Functional Loss SNV dbSNP153 33..33 33 - - - 25937 RMVar_ID_25937 Human_SNP_ID_159485533 A-to-I Human chr3 + 155993031 155993031 155993031 CTCCCACCTCAGCCTCTGGAGTTGCTGGGACCACAGGTGCACGCCACCATGCCTGGCTAATTTTT CTCCCACCTCAGCCTCTGGAGTTGCTGGGACCGCAGGTGCACGCCACCATGCCTGGCTAATTTTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1473487479 Functional Loss SNV dbSNP153 33..33 33 - - - 25938 RMVar_ID_25938 Human_SNP_ID_159608804 A-to-I Human chr3 - 156531140 156531140 156531140 CAATGGATTGTAAGATTCTCTCCAGCACGCTCAGCTGCCCTCAAGTAGAAGCAGAAAACACAGAT CAATGGATTGTAAGATTCTCTCCAGCACGCTCGGCTGCCCTCAAGTAGAAGCAGAAAACACAGAT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1458130944 Functional Loss SNV dbSNP153 33..33 33 - - - 25939 RMVar_ID_25939 Human_SNP_ID_159611198 A-to-I Human chr3 - 156540416 156540416 156540416 TATTTTTAGTAGAGACGGGGTTTCACCCTGTTAGCCAGGATGGTCTCGATCTCCTGACCTCGTGA TATTTTTAGTAGAGACGGGGTTTCACCCTGTTGGCCAGGATGGTCTCGATCTCCTGACCTCGTGA T C SSR3 Ensembl:ENSG00000114850 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1129125 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_154523 Human_miRNA_ID_337489,Human_miRNA_ID_794985 RMVar_hsa_circ_79315,RMVar_hsa_circ_222336 25940 RMVar_ID_25940 Human_SNP_ID_159611208 A-to-I Human chr3 - 156540441 156540441 156540441 CCACCACACCCGGCTAATTTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCCTGTTAGCCAGGA CCACCACACCCGGCTAATTTTTTTGTATTTTTGGTAGAGACGGGGTTTCACCCTGTTAGCCAGGA T C SSR3 Ensembl:ENSG00000114850 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,31158229,31158229 RNA-Seq:(High) rs1340068571 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79315,RMVar_hsa_circ_222336 25941 RMVar_ID_25941 Human_SNP_ID_159611226 A-to-I Human chr3 - 156540484 156540484 156540484 CTCCTGCCTCAGCCTGCCGAGTAGCTGGGACTACAGGCGCCCGCCACCACACCCGGCTAATTTTT CTCCTGCCTCAGCCTGCCGAGTAGCTGGGACTGCAGGCGCCCGCCACCACACCCGGCTAATTTTT T C SSR3 Ensembl:ENSG00000114850 Protein coding 3'UTR GSE47997;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,29796672,31158229,31158229,31158229 RNA-Seq:(High) rs1243145852 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79315,RMVar_hsa_circ_222336 25942 RMVar_ID_25942 Human_SNP_ID_159611227 A-to-I Human chr3 - 156540494 156540494 156540494 TCACGCCATTCTCCTGCCTCAGCCTGCCGAGTAGCTGGGACTACAGGCGCCCGCCACCACACCCG TCACGCCATTCTCCTGCCTCAGCCTGCCGAGTGGCTGGGACTACAGGCGCCCGCCACCACACCCG T C SSR3 Ensembl:ENSG00000114850 Protein coding 3'UTR GSE47997;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,29796672,31158229,31158229,31158229 RNA-Seq:(High) rs1197966013 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79315,RMVar_hsa_circ_222336 25943 RMVar_ID_25943 Human_SNP_ID_159611231 A-to-I Human chr3 - 156540519 156540519 156540519 TCACTGCGAGCTCCGCCTCCCAGGTTCACGCCATTCTCCTGCCTCAGCCTGCCGAGTAGCTGGGA TCACTGCGAGCTCCGCCTCCCAGGTTCACGCCGTTCTCCTGCCTCAGCCTGCCGAGTAGCTGGGA T C SSR3 Ensembl:ENSG00000114850 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE99789;GSE112787;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;293 Flip-In T-REx cells,empty vector;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,29129909,29796672,29967493,31158229,31158229,32596459 RNA-Seq:(High) rs1360832539 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79315,RMVar_hsa_circ_222336 25944 RMVar_ID_25944 Human_SNP_ID_159611238 A-to-I Human chr3 - 156540530 156540530 156540530 TCTATCTTGGCTCACTGCGAGCTCCGCCTCCCAGGTTCACGCCATTCTCCTGCCTCAGCCTGCCG TCTATCTTGGCTCACTGCGAGCTCCGCCTCCCGGGTTCACGCCATTCTCCTGCCTCAGCCTGCCG T C SSR3 Ensembl:ENSG00000114850 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs1445281794 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2723290 RMVar_hsa_circ_79315,RMVar_hsa_circ_222336 25945 RMVar_ID_25945 Human_SNP_ID_159611263 A-to-I Human chr3 - 156540600 156540600 156540600 TATTCTTTTTTTTTTTTTTTTTTTTTTGAGACAGCGTCTCGCTCTGTCACCCAGGCTGGAGTACA TATTCTTTTTTTTTTTTTTTTTTTTTTGAGACGGCGTCTCGCTCTGTCACCCAGGCTGGAGTACA T C SSR3 Ensembl:ENSG00000114850 Protein coding 3'UTR GSE47997;GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,24183664,31158229,31158229,31158229 RNA-Seq:(High) rs1257876483 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79315,RMVar_hsa_circ_222336 25946 RMVar_ID_25946 Human_SNP_ID_159611271 A-to-I Human chr3 - 156540604 156540604 156540604 TTGATATTCTTTTTTTTTTTTTTTTTTTTTTGAGACAGCGTCTCGCTCTGTCACCCAGGCTGGAG TTGATATTCTTTTTTTTTTTTTTTTTTTTTTGTGACAGCGTCTCGCTCTGTCACCCAGGCTGGAG T A SSR3 Ensembl:ENSG00000114850 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1181182654 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79315,RMVar_hsa_circ_222336 25947 RMVar_ID_25947 Human_SNP_ID_159611272 A-to-I Human chr3 - 156540604 156540604 156540604 TTGATATTCTTTTTTTTTTTTTTTTTTTTTTGAGACAGCGTCTCGCTCTGTCACCCAGGCTGGAG TTGATATTCTTTTTTTTTTTTTTTTTTTTTTGGGACAGCGTCTCGCTCTGTCACCCAGGCTGGAG T C SSR3 Ensembl:ENSG00000114850 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1181182654 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79315,RMVar_hsa_circ_222336 25948 RMVar_ID_25948 Human_SNP_ID_159611512 A-to-I Human chr3 - 156541440 156541440 156541440 TACTACTGCCTGGGTGGCAAGGGTGAGACTCCATCTCAAAAAAGAAACAAAAAAACCCAAAAAGT TACTACTGCCTGGGTGGCAAGGGTGAGACTCCGTCTCAAAAAAGAAACAAAAAAACCCAAAAAGT T C SSR3 Ensembl:ENSG00000114850 Protein coding 3'UTR GSE38233;GSE100210;GSE99789;GSE112787;GSE107867;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;293 Flip-In T-REx cells,empty vector;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,29796672,29967493,30559470,32596459 RNA-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 25949 RMVar_ID_25949 Human_SNP_ID_159611527 A-to-I Human chr3 - 156541499 156541499 156541499 TGAAGCAGGAGAACTGCCTGAACCCAGGAGGCAGAGGTTGCGGTGAGTCGAGATCGTGCTACTAC TGAAGCAGGAGAACTGCCTGAACCCAGGAGGCGGAGGTTGCGGTGAGTCGAGATCGTGCTACTAC T C SSR3 Ensembl:ENSG00000114850 Protein coding 3'UTR GSE38233;GSE100210;GSE112787 cultured B-cells;HepG2 cell line;293 Flip-In T-REx cells,empty vector - 24183664,29129909,29967493 RNA-Seq:(High) rs1129107 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26504917 RMVar_hsa_circ_79315,RMVar_hsa_circ_222336 25950 RMVar_ID_25950 Human_SNP_ID_159611528 A-to-I Human chr3 - 156541503 156541503 156541503 AGGCTGAAGCAGGAGAACTGCCTGAACCCAGGAGGCAGAGGTTGCGGTGAGTCGAGATCGTGCTA AGGCTGAAGCAGGAGAACTGCCTGAACCCAGGGGGCAGAGGTTGCGGTGAGTCGAGATCGTGCTA T C SSR3 Ensembl:ENSG00000114850 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1410058110 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26510619 RMVar_hsa_circ_79315,RMVar_hsa_circ_222336 25951 RMVar_ID_25951 Human_SNP_ID_159611529 A-to-I Human chr3 - 156541506 156541506 156541506 GGGAGGCTGAAGCAGGAGAACTGCCTGAACCCAGGAGGCAGAGGTTGCGGTGAGTCGAGATCGTG GGGAGGCTGAAGCAGGAGAACTGCCTGAACCCGGGAGGCAGAGGTTGCGGTGAGTCGAGATCGTG T C SSR3 Ensembl:ENSG00000114850 Protein coding 3'UTR GSE38233;GSE100210;GSE112787 cultured B-cells;HepG2 cell line;293 Flip-In T-REx cells,empty vector - 24183664,29129909,29967493 RNA-Seq:(High) rs1129105 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26510619 RMVar_hsa_circ_79315,RMVar_hsa_circ_222336 25952 RMVar_ID_25952 Human_SNP_ID_159611531 A-to-I Human chr3 - 156541510 156541510 156541510 ACTTGGGAGGCTGAAGCAGGAGAACTGCCTGAACCCAGGAGGCAGAGGTTGCGGTGAGTCGAGAT ACTTGGGAGGCTGAAGCAGGAGAACTGCCTGAGCCCAGGAGGCAGAGGTTGCGGTGAGTCGAGAT T C SSR3 Ensembl:ENSG00000114850 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1129104 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26510619 RMVar_hsa_circ_79315,RMVar_hsa_circ_222336 25953 RMVar_ID_25953 Human_SNP_ID_159611536 A-to-I Human chr3 - 156541528 156541528 156541528 GCGCCTGTAATCTCAGCTACTTGGGAGGCTGAAGCAGGAGAACTGCCTGAACCCAGGAGGCAGAG GCGCCTGTAATCTCAGCTACTTGGGAGGCTGAGGCAGGAGAACTGCCTGAACCCAGGAGGCAGAG T C SSR3 Ensembl:ENSG00000114850 Protein coding 3'UTR GSE38233;GSE112787;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;293 Flip-In T-REx cells,empty vector;Bronchiolar epithelium,BEP2D cell line - 24183664,29967493,31158229 RNA-Seq:(High) rs1201890739 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26510619 RMVar_hsa_circ_79315,RMVar_hsa_circ_222336 25954 RMVar_ID_25954 Human_SNP_ID_159611546 A-to-I Human chr3 - 156541551 156541551 156541551 AAATTAGCCAGGCGTGATGGTGGGCGCCTGTAATCTCAGCTACTTGGGAGGCTGAAGCAGGAGAA AAATTAGCCAGGCGTGATGGTGGGCGCCTGTAGTCTCAGCTACTTGGGAGGCTGAAGCAGGAGAA T C SSR3 Ensembl:ENSG00000114850 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1129099 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26510619 RMVar_hsa_circ_79315,RMVar_hsa_circ_222336 25955 RMVar_ID_25955 Human_SNP_ID_159611547 A-to-I Human chr3 - 156541552 156541552 156541552 AAAATTAGCCAGGCGTGATGGTGGGCGCCTGTAATCTCAGCTACTTGGGAGGCTGAAGCAGGAGA AAAATTAGCCAGGCGTGATGGTGGGCGCCTGTGATCTCAGCTACTTGGGAGGCTGAAGCAGGAGA T C SSR3 Ensembl:ENSG00000114850 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1129097 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26511387 RMVar_hsa_circ_79315,RMVar_hsa_circ_222336 25956 RMVar_ID_25956 Human_SNP_ID_159611557 A-to-I Human chr3 - 156541574 156541574 156541574 CCCCGTCTCTACTAAAAATACCAAAATTAGCCAGGCGTGATGGTGGGCGCCTGTAATCTCAGCTA CCCCGTCTCTACTAAAAATACCAAAATTAGCCGGGCGTGATGGTGGGCGCCTGTAATCTCAGCTA T C SSR3 Ensembl:ENSG00000114850 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1129091 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79315,RMVar_hsa_circ_222336 25957 RMVar_ID_25957 Human_SNP_ID_159611559 A-to-I Human chr3 - 156541578 156541578 156541578 GAAACCCCGTCTCTACTAAAAATACCAAAATTAGCCAGGCGTGATGGTGGGCGCCTGTAATCTCA GAAACCCCGTCTCTACTAAAAATACCAAAATTGGCCAGGCGTGATGGTGGGCGCCTGTAATCTCA T C SSR3 Ensembl:ENSG00000114850 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,31158229,31158229 RNA-Seq:(High) rs1184938873 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79315,RMVar_hsa_circ_222336 25958 RMVar_ID_25958 Human_SNP_ID_159611570 A-to-I Human chr3 - 156541615 156541615 156541615 TTTAAAAAACTTTTCTTGAACTCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATACCAA TTTAAAAAACTTTTCTTGAACTCCTGGCCAACGTGGTGAAACCCCGTCTCTACTAAAAATACCAA T C SSR3 Ensembl:ENSG00000114850 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs918703430 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_154525,Human_RBP_ID_593577,Human_RBP_ID_7143720,Human_RBP_ID_8563050,Human_RBP_ID_14690114,Human_RBP_ID_17997659,Human_RBP_ID_22397636,Human_RBP_ID_23312364,Human_RBP_ID_24496398,Human_RBP_ID_26510620 Human_miRNA_ID_2709613 RMVar_hsa_circ_79315,RMVar_hsa_circ_222336 25959 RMVar_ID_25959 Human_SNP_ID_159611572 A-to-I Human chr3 - 156541617 156541617 156541617 TTTTTAAAAAACTTTTCTTGAACTCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATACC TTTTTAAAAAACTTTTCTTGAACTCCTGGCCAGCATGGTGAAACCCCGTCTCTACTAAAAATACC T C SSR3 Ensembl:ENSG00000114850 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1046619 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_593577,Human_RBP_ID_7143720,Human_RBP_ID_8563050,Human_RBP_ID_14690114,Human_RBP_ID_17997659,Human_RBP_ID_22397636,Human_RBP_ID_23312364,Human_RBP_ID_24496398,Human_RBP_ID_26510620 Human_miRNA_ID_2709613 RMVar_hsa_circ_79315,RMVar_hsa_circ_222336 25960 RMVar_ID_25960 Human_SNP_ID_159611573 A-to-I Human chr3 - 156541618 156541618 156541618 ATTTTTAAAAAACTTTTCTTGAACTCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATAC ATTTTTAAAAAACTTTTCTTGAACTCCTGGCCTACATGGTGAAACCCCGTCTCTACTAAAAATAC T A SSR3 Ensembl:ENSG00000114850 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1046618 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_593577,Human_RBP_ID_7143720,Human_RBP_ID_8563050,Human_RBP_ID_14690114,Human_RBP_ID_17997659,Human_RBP_ID_22397636,Human_RBP_ID_23312364,Human_RBP_ID_24496398,Human_RBP_ID_26510620 Human_miRNA_ID_1348377,Human_miRNA_ID_1811732,Human_miRNA_ID_2709613 RMVar_hsa_circ_79315,RMVar_hsa_circ_222336 25961 RMVar_ID_25961 Human_SNP_ID_159611574 A-to-I Human chr3 - 156541618 156541618 156541618 ATTTTTAAAAAACTTTTCTTGAACTCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATAC ATTTTTAAAAAACTTTTCTTGAACTCCTGGCCGACATGGTGAAACCCCGTCTCTACTAAAAATAC T C SSR3 Ensembl:ENSG00000114850 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1046618 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_593577,Human_RBP_ID_7143720,Human_RBP_ID_8563050,Human_RBP_ID_14690114,Human_RBP_ID_17997659,Human_RBP_ID_22397636,Human_RBP_ID_23312364,Human_RBP_ID_24496398,Human_RBP_ID_26510620 Human_miRNA_ID_1348377,Human_miRNA_ID_1811732,Human_miRNA_ID_2709613 RMVar_hsa_circ_79315,RMVar_hsa_circ_222336 25962 RMVar_ID_25962 Human_SNP_ID_159672668 A-to-I Human chr3 - 156809649 156809649 156809649 ATGCAGAGCTAAAGGCCCTCCTCCAGAGTTCTACAAGTCGAAAAACCCAGAAAAAGAAAACAAAG ATGCAGAGCTAAAGGCCCTCCTCCAGAGTTCTGCAAGTCGAAAAACCCAGAAAAAGAAAACAAAG T C LINC00886,PA2G4P4 Ensembl:ENSG00000240875,Ensembl:ENSG00000230457 lincRNA,Pseudogene intron,exon GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs878940517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3723112,Human_RBP_ID_7237182,Human_RBP_ID_8125012,Human_RBP_ID_17406498 25963 RMVar_ID_25963 Human_SNP_ID_159672669 A-to-I Human chr3 - 156809649 156809649 156809649 ATGCAGAGCTAAAGGCCCTCCTCCAGAGTTCTACAAGTCGAAAAACCCAGAAAAAGAAAACAAAG ATGCAGAGCTAAAGGCCCTCCTCCAGAGTTCTCCAAGTCGAAAAACCCAGAAAAAGAAAACAAAG T G LINC00886,PA2G4P4 Ensembl:ENSG00000240875,Ensembl:ENSG00000230457 lincRNA,Pseudogene intron,exon GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs878940517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3723112,Human_RBP_ID_7237182,Human_RBP_ID_8125012,Human_RBP_ID_17406498 25964 RMVar_ID_25964 Human_SNP_ID_159752483 A-to-I Human chr3 - 157150987 157150987 157150987 CATTAATAAAAGTTCAGCAATTTTTTAACTGAAATAGTTTATCTCTTTTACCTAGTCACAAAAAA CATTAATAAAAGTTCAGCAATTTTTTAACTGAGATAGTTTATCTCTTTTACCTAGTCACAAAAAA T C CCNL1 Ensembl:ENSG00000163660 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs573836210 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14691154,Human_RBP_ID_23019246 RMVar_hsa_circ_12973,RMVar_hsa_circ_222348,RMVar_hsa_circ_110601,RMVar_hsa_circ_332387,RMVar_hsa_circ_52715 25965 RMVar_ID_25965 Human_SNP_ID_159758999 A-to-I Human chr3 + 157176354 157176354 157176354 CCAGAGGGCCTGGGTCTGTGGCTCATGCCTGTAATTCCAGCACTTTGGGAGGCTGAGGCGGAGGA CCAGAGGGCCTGGGTCTGTGGCTCATGCCTGTTATTCCAGCACTTTGGGAGGCTGAGGCGGAGGA A T AC092944.1 Ensembl:ENSG00000243176 lincRNA exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1379556081 Functional Loss SNV dbSNP153 33..33 33 - - - 25966 RMVar_ID_25966 Human_SNP_ID_159764917 A-to-I Human chr3 + 157198000 157198000 157198000 ATACATTCTTTTTTTTTTTTTTTTTTTGAGACAAAGTCTCACTCTGTTGCCCAGGCTGGAGGGCA ATACATTCTTTTTTTTTTTTTTTTTTTGAGACGAAGTCTCACTCTGTTGCCCAGGCTGGAGGGCA A G AC092944.1 Ensembl:ENSG00000243176 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1451534740 Functional Loss SNV dbSNP153 33..33 33 - - - 25967 RMVar_ID_25967 Human_SNP_ID_159983420 A-to-I Human chr3 + 158106013 158106013 158106013 TTCTGGTCAAAAGACTTGGAGACGAACGCCGTAAGTTCTTCCATCGCCGCCGCACGTCAGCCCGG TTCTGGTCAAAAGACTTGGAGACGAACGCCGTTAGTTCTTCCATCGCCGCCGCACGTCAGCCCGG A T RSRC1 Ensembl:ENSG00000174891 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444643706 Functional Loss SNV dbSNP153 33..33 33 - - - 25968 RMVar_ID_25968 Human_SNP_ID_160035097 A-to-I Human chr3 + 158314160 158314160 158314160 TTACCCAGGCTGGAGTGCAGTGGCACGATCTCAGCTCACCGCAATCTCTGCCTCCCTGATTCAAG TTACCCAGGCTGGAGTGCAGTGGCACGATCTCTGCTCACCGCAATCTCTGCCTCCCTGATTCAAG A T RSRC1 Ensembl:ENSG00000174891 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs555957063 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24622,RMVar_hsa_circ_357129,RMVar_hsa_circ_126924,RMVar_hsa_circ_119544,RMVar_hsa_circ_222360,RMVar_hsa_circ_222361,RMVar_hsa_circ_25858 25969 RMVar_ID_25969 Human_SNP_ID_160056460 A-to-I Human chr3 + 158401069 158401069 158401069 CTACCCATAGTATTCAGGTACAGTAACATGCTATACAGCTTTGTAGCCTAGAAACAGTAGGCTAT CTACCCATAGTATTCAGGTACAGTAACATGCTGTACAGCTTTGTAGCCTAGAAACAGTAGGCTAT A G RSRC1 Ensembl:ENSG00000174891 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs575976801 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126924,RMVar_hsa_circ_119544,RMVar_hsa_circ_222360,RMVar_hsa_circ_222361,RMVar_hsa_circ_25858 25970 RMVar_ID_25970 Human_SNP_ID_160066772 A-to-I Human chr3 + 158442868 158442868 158442868 AAGTCAATTTTTCTGTGATCTGTGGGCTGCAAAATGAATGTTCTGTTAGCAGGCGTGAAAACAGC AAGTCAATTTTTCTGTGATCTGTGGGCTGCAATATGAATGTTCTGTTAGCAGGCGTGAAAACAGC A T RSRC1 Ensembl:ENSG00000174891 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs529821581 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126924,RMVar_hsa_circ_119544,RMVar_hsa_circ_222360,RMVar_hsa_circ_222361,RMVar_hsa_circ_25858 25971 RMVar_ID_25971 Human_SNP_ID_160090994 A-to-I Human chr3 + 158544786 158544785 158544786 CAGAATGTGCATGTTAAAGAACATATTTATGGAAAAAAAATTTTTGAAACTTAAATAAATTGGTG CAGAATGTGCATGTTAAAGAACATATTTATGG_AAAAAAATTTTTGAAACTTAAATAAATTGGTG GA G RSRC1 Ensembl:ENSG00000174891 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1383438734 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_14696055 25972 RMVar_ID_25972 Human_SNP_ID_160106756 A-to-I Human chr3 + 158608552 158608549 158608553 TTAAAATGGTTTATAGACTATCATAAACTGATACATACAAATATGATTGTGGGATATAGACATTA TTAAAATGGTTTATAGACTATCATAAACTG____ATACAAATATGATTGTGGGATATAGACATTA GATAC G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1362826948 Functional Loss DEL dbSNP153 31..34 33 - - - 25973 RMVar_ID_25973 Human_SNP_ID_160106758 A-to-I Human chr3 + 158608552 158608552 158608552 TTAAAATGGTTTATAGACTATCATAAACTGATACATACAAATATGATTGTGGGATATAGACATTA TTAAAATGGTTTATAGACTATCATAAACTGATGCATACAAATATGATTGTGGGATATAGACATTA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs550926314 Functional Loss SNV dbSNP153 33..33 33 - - - 25974 RMVar_ID_25974 Human_SNP_ID_160106761 A-to-I Human chr3 + 158608562 158608562 158608562 TTATAGACTATCATAAACTGATACATACAAATATGATTGTGGGATATAGACATTAATAATCCTTT TTATAGACTATCATAAACTGATACATACAAATGTGATTGTGGGATATAGACATTAATAATCCTTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1422755175 Functional Loss SNV dbSNP153 33..33 33 - - - 25975 RMVar_ID_25975 Human_SNP_ID_160123306 A-to-I Human chr3 + 158674220 158674220 158674220 CTCCTGCCTCAGCCTCCCTAGTATCTGGGACTACAGGTGCACTTCACCACACCTGGCTAATTTTT CTCCTGCCTCAGCCTCCCTAGTATCTGGGACTGCAGGTGCACTTCACCACACCTGGCTAATTTTT A G GFM1 Ensembl:ENSG00000168827 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992787738 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_222372,RMVar_hsa_circ_82359,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_363369,RMVar_hsa_circ_354771,RMVar_hsa_circ_222381,RMVar_hsa_circ_222382,RMVar_hsa_circ_360281,RMVar_hsa_circ_222384 25976 RMVar_ID_25976 Human_SNP_ID_160128315 A-to-I Human chr3 + 158695267 158695267 158695267 GGGGTGGCTCACGCCTGTAGCCCCAGCTGCTCAGGAGGCTGAGGCAGGAGGGTCGCTTGAACCCG GGGGTGGCTCACGCCTGTAGCCCCAGCTGCTCGGGAGGCTGAGGCAGGAGGGTCGCTTGAACCCG A G GFM1 Ensembl:ENSG00000168827 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs923892390 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_222378 25977 RMVar_ID_25977 Human_SNP_ID_160128330 A-to-I Human chr3 + 158695313 158695313 158695313 GGAGGGTCGCTTGAACCCGGAAGGCGGAGGCTATAGTGAGCTGAGATGGCACCACTGCACTCCAG GGAGGGTCGCTTGAACCCGGAAGGCGGAGGCTGTAGTGAGCTGAGATGGCACCACTGCACTCCAG A G GFM1 Ensembl:ENSG00000168827 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs553567669 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_593891,Human_RBP_ID_14697010 RMVar_hsa_circ_222378 25978 RMVar_ID_25978 Human_SNP_ID_160265487 A-to-I Human chr3 + 159284711 159284711 159284711 TAGAGATTGGGTTTCATCATGTTGGCCAGGCTAGTCTCGAACTTGTGACCTCAGATGATCTGCTT TAGAGATTGGGTTTCATCATGTTGGCCAGGCTGGTCTCGAACTTGTGACCTCAGATGATCTGCTT A G IQCJ-SCHIP1 Ensembl:ENSG00000283154 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1199993380 Functional Loss SNV dbSNP153 33..33 33 - - - 25979 RMVar_ID_25979 Human_SNP_ID_160306154 A-to-I Human chr3 + 159448812 159448812 159448812 CTAACACACTCATGAACTCATGTGGTGCTCACAACAGCATCGTGAGGTAGTCCAGGAGTGGATGG CTAACACACTCATGAACTCATGTGGTGCTCACGACAGCATCGTGAGGTAGTCCAGGAGTGGATGG A G IQCJ-SCHIP1 Ensembl:ENSG00000283154 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1200357712 Functional Loss SNV dbSNP153 33..33 33 - - - 25980 RMVar_ID_25980 Human_SNP_ID_160312269 A-to-I Human chr3 + 159475278 159475278 159475278 AACAGGAATGAAGTACTGATACATGTTACAATATGGATGAACCTTGAAAATTATGCTGAATGAAA AACAGGAATGAAGTACTGATACATGTTACAATGTGGATGAACCTTGAAAATTATGCTGAATGAAA A G IQCJ-SCHIP1 Ensembl:ENSG00000283154 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1486797200 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_222402 25981 RMVar_ID_25981 Human_SNP_ID_160312383 A-to-I Human chr3 + 159475871 159475871 159475871 GAAACAGGAATTAAGGCAAAAGTTATGGCAGGAGTTGAAGCTTTCATAACAAGGTCTTGGGAAAA GAAACAGGAATTAAGGCAAAAGTTATGGCAGGGGTTGAAGCTTTCATAACAAGGTCTTGGGAAAA A G IQCJ-SCHIP1 Ensembl:ENSG00000283154 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1373787196 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9134601 RMVar_hsa_circ_222402 25982 RMVar_ID_25982 Human_SNP_ID_160341647 A-to-I Human chr3 + 159591499 159591499 159591499 ACATATGCTTATTGCAGCACTATTTACAATAGAAAAGACATGGAAGCAACCCAAATGCCCATCAA ACATATGCTTATTGCAGCACTATTTACAATAGCAAAGACATGGAAGCAACCCAAATGCCCATCAA A C IQCJ-SCHIP1 Ensembl:ENSG00000283154 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs530970102 Functional Loss SNV dbSNP153 33..33 33 - - - 25983 RMVar_ID_25983 Human_SNP_ID_160494972 A-to-I Human chr3 - 160227356 160227356 160227356 TCTTCTCAAATAGTGAAAATAAGATATCCTTCATGTTTTTTATGTCACATATGCTTCCTCGTTTG TCTTCTCAAATAGTGAAAATAAGATATCCTTCGTGTTTTTTATGTCACATATGCTTCCTCGTTTG T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs532718589 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3693774 25984 RMVar_ID_25984 Human_SNP_ID_160505351 A-to-I Human chr3 - 160274545 160274545 160274545 ATTATATACTTCCTGAAGAGCGGAAACATTTCACATTATCTATACATAGTAGGTAGTTAATATTC ATTATATACTTCCTGAAGAGCGGAAACATTTCCCATTATCTATACATAGTAGGTAGTTAATATTC T G IFT80,AC079594.2 Ensembl:ENSG00000068885,Ensembl:ENSG00000248710 Protein coding,Protein coding intron,intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs985898337 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_501292,Human_Splice_Rec_501293 RMVar_hsa_circ_21916,RMVar_hsa_circ_46111,RMVar_hsa_circ_267418,RMVar_hsa_circ_301171,RMVar_hsa_circ_30262,RMVar_hsa_circ_10022,RMVar_hsa_circ_311130,RMVar_hsa_circ_346892,RMVar_hsa_circ_222409,RMVar_hsa_circ_362380,RMVar_hsa_circ_334504,RMVar_hsa_circ_36033,RMVar_hsa_circ_222410 25985 RMVar_ID_25985 Human_SNP_ID_160520830 A-to-I Human chr3 - 160342853 160342853 160342853 CTAGTTTATTTGGTTTGCCACCAGGAGTCACTATGTTGTTCTTTGTTTTATATACATAAGCATAT CTAGTTTATTTGGTTTGCCACCAGGAGTCACTGTGTTGTTCTTTGTTTTATATACATAAGCATAT T C IFT80,AC079594.2 Ensembl:ENSG00000068885,Ensembl:ENSG00000248710 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1278504190 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_213,RMVar_hsa_circ_21916,RMVar_hsa_circ_67794,RMVar_hsa_circ_362380,RMVar_hsa_circ_367255,RMVar_hsa_circ_101625,RMVar_hsa_circ_72310,RMVar_hsa_circ_222413,RMVar_hsa_circ_70744,RMVar_hsa_circ_325672,RMVar_hsa_circ_57658,RMVar_hsa_circ_222417,RMVar_hsa_circ_11066,RMVar_hsa_circ_363009,RMVar_hsa_circ_13283,RMVar_hsa_circ_51303,RMVar_hsa_circ_299970,RMVar_hsa_circ_325393,RMVar_hsa_circ_375357,RMVar_hsa_circ_222418,RMVar_hsa_circ_332416,RMVar_hsa_circ_222419 25986 RMVar_ID_25986 Human_SNP_ID_160537362 A-to-I Human chr3 + 160411916 160411916 160411916 TACACAGTGAGTATGAAATATAACTTTTTTTTAAAGGGTGAAGTTGAACAAATTGCTATGATGAA TACACAGTGAGTATGAAATATAACTTTTTTTTGAAGGGTGAAGTTGAACAAATTGCTATGATGAA A G SMC4 Ensembl:ENSG00000113810 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs377286985 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_69736,Human_RBP_ID_2760820,Human_RBP_ID_25709789 Human_Splice_Rec_501749 RMVar_hsa_circ_31710,RMVar_hsa_circ_62770,RMVar_hsa_circ_18861,RMVar_hsa_circ_14555,RMVar_hsa_circ_357246,RMVar_hsa_circ_357820,RMVar_hsa_circ_222426 25987 RMVar_ID_25987 Human_SNP_ID_160537609 A-to-I Human chr3 + 160412683 160412683 160412683 TGGGAGTTCAAGACCAGCCTGGGCAACATAGCAAGACCCCATCTCTACAAAAAAAGGAATTATGT TGGGAGTTCAAGACCAGCCTGGGCAACATAGCCAGACCCCATCTCTACAAAAAAAGGAATTATGT A C SMC4 Ensembl:ENSG00000113810 Protein coding exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs193278662 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4254,RMVar_hsa_circ_31710,RMVar_hsa_circ_62770,RMVar_hsa_circ_18861,RMVar_hsa_circ_331574,RMVar_hsa_circ_14555,RMVar_hsa_circ_357246,RMVar_hsa_circ_357820,RMVar_hsa_circ_349415,RMVar_hsa_circ_373315,RMVar_hsa_circ_222426,RMVar_hsa_circ_333471,RMVar_hsa_circ_73889,RMVar_hsa_circ_279627,RMVar_hsa_circ_65042,RMVar_hsa_circ_63566,RMVar_hsa_circ_222427,RMVar_hsa_circ_222428,RMVar_hsa_circ_222429,RMVar_hsa_circ_67271,RMVar_hsa_circ_359771 25988 RMVar_ID_25988 Human_SNP_ID_160544241 A-to-I Human chr3 + 160435383 160435383 160435383 GCCTCAGCCTCCCAAAGTGCTGGACTATAGGCATGAGCCACTGCACCCAGCCTGCAGTACTAAGT GCCTCAGCCTCCCAAAGTGCTGGACTATAGGCGTGAGCCACTGCACCCAGCCTGCAGTACTAAGT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs979522409 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14703321 25989 RMVar_ID_25989 Human_SNP_ID_160544242 A-to-I Human chr3 + 160435383 160435383 160435383 GCCTCAGCCTCCCAAAGTGCTGGACTATAGGCATGAGCCACTGCACCCAGCCTGCAGTACTAAGT GCCTCAGCCTCCCAAAGTGCTGGACTATAGGCTTGAGCCACTGCACCCAGCCTGCAGTACTAAGT A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs979522409 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14703321 25990 RMVar_ID_25990 Human_SNP_ID_160560665 A-to-I Human chr3 - 160503864 160503864 160503864 TGCCCTGGCTGAGCTTGAACTCCTGGACTCAAACAATTCTCCCATCTTGGCCTCCCAAAGTGCTG TGCCCTGGCTGAGCTTGAACTCCTGGACTCAAGCAATTCTCCCATCTTGGCCTCCCAAAGTGCTG T C KPNA4 Ensembl:ENSG00000186432 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs746018966 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14703841 RMVar_hsa_circ_101108,RMVar_hsa_circ_222439 25991 RMVar_ID_25991 Human_SNP_ID_160562792 A-to-I Human chr3 - 160512769 160512769 160512769 AGAGTGCAGTGACACGATATCAGCTCACTGCAATCTCTACCTCCCGGGTTTAGGCGATTCTTGCG AGAGTGCAGTGACACGATATCAGCTCACTGCACTCTCTACCTCCCGGGTTTAGGCGATTCTTGCG T G KPNA4 Ensembl:ENSG00000186432 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1007846342 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25710342 RMVar_hsa_circ_340156,RMVar_hsa_circ_73918,RMVar_hsa_circ_222441,RMVar_hsa_circ_108637,RMVar_hsa_circ_337111 25992 RMVar_ID_25992 Human_SNP_ID_160562997 A-to-I Human chr3 - 160513407 160513407 160513407 TTTTTTTAAAAAAGAAATTAGTTTGGTGTGGTAGCATGCGCCTGTGGTTCTAGCTACTTGGGAAG TTTTTTTAAAAAAGAAATTAGTTTGGTGTGGTGGCATGCGCCTGTGGTTCTAGCTACTTGGGAAG T C KPNA4 Ensembl:ENSG00000186432 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs963009486 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_340156,RMVar_hsa_circ_73918,RMVar_hsa_circ_222441,RMVar_hsa_circ_108637,RMVar_hsa_circ_337111 25993 RMVar_ID_25993 Human_SNP_ID_160575884 A-to-I Human chr3 - 160565273 160565273 160565273 GGGAAGGAGTCACCGGCCCGGCCATGGCGGACAACGAGAAACTGGACAACCAACGGCTCAAGAAT GGGAAGGAGTCACCGGCCCGGCCATGGCGGACTACGAGAAACTGGACAACCAACGGCTCAAGAAT T A KPNA4 Ensembl:ENSG00000186432 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs766838806 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_212755,Human_RBP_ID_1621702,Human_RBP_ID_1954576,Human_RBP_ID_2761287,Human_RBP_ID_4757541,Human_RBP_ID_9434949,Human_RBP_ID_14704589,Human_RBP_ID_18954688,Human_RBP_ID_23981726,Human_RBP_ID_27823636 Human_Splice_Rec_501843,Human_Splice_Rec_501883 RMVar_hsa_circ_222447 25994 RMVar_ID_25994 Human_SNP_ID_160745213 A-to-I Human chr3 + 161289193 161289193 161289193 GATTCTCATGCCTCAGCCTCCTGAGTAGCTGGAACTACAGGCACGTGCCACCACACTTGGCTACT GATTCTCATGCCTCAGCCTCCTGAGTAGCTGGTACTACAGGCACGTGCCACCACACTTGGCTACT A T lnc-NMD3-2,lnc-NMD3-2:2 RNACentral:URS00008BEFF1,RNACentral:URS00009B57B6 lincRNA,lincRNA exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256093530 Functional Loss SNV dbSNP153 33..33 33 - - - 25995 RMVar_ID_25995 Human_SNP_ID_160826247 A-to-I Human chr3 + 161627719 161627719 161627719 AATACTATCAGATCTCATGAGACTCAGTCACTATCACAAGAACAGCATGGGAAAACCTGGCCCTA AATACTATCAGATCTCATGAGACTCAGTCACTGTCACAAGAACAGCATGGGAAAACCTGGCCCTA A G AC112770.1 Ensembl:ENSG00000288087 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1329422114 Functional Loss SNV dbSNP153 33..33 33 - - - 25996 RMVar_ID_25996 Human_SNP_ID_686601267 A-to-I Human chr20 + 62124980 62124980 62124980 TCAGCTCATTGCAACTTTGGCTTCCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGC TCAGCTCATTGCAACTTTGGCTTCCCAGGTTCCAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGC A C LSM14B Ensembl:ENSG00000149657 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs961484300 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120149,RMVar_hsa_circ_211150,RMVar_hsa_circ_273625,RMVar_hsa_circ_211148,RMVar_hsa_circ_281693,RMVar_hsa_circ_211151 25997 RMVar_ID_25997 Human_SNP_ID_686602381 A-to-I Human chr20 + 62129116 62129116 62129116 GGTTCATCCCCTGTGCGTGGGCCTCGGACTGCAGTTTCATAGGCATAGCCCCTTGCCAAAGGCTA GGTTCATCCCCTGTGCGTGGGCCTCGGACTGCGGTTTCATAGGCATAGCCCCTTGCCAAAGGCTA A G LSM14B Ensembl:ENSG00000149657 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs564687440 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22601504 RMVar_hsa_circ_123618,RMVar_hsa_circ_120149,RMVar_hsa_circ_211148,RMVar_hsa_circ_281693,RMVar_hsa_circ_211151,RMVar_hsa_circ_211152 25998 RMVar_ID_25998 Human_SNP_ID_686613510 A-to-I Human chr20 + 62162484 62162484 62162484 CCACCACACCTGGCTAATTTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGTCCAGGC CCACCACACCTGGCTAATTTTTTTGTATTTTTGGTAGAGACGGGGTTTCACCATGTTGTCCAGGC A G SS18L1 Ensembl:ENSG00000184402 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1055325734 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21003,RMVar_hsa_circ_334669,RMVar_hsa_circ_211164,RMVar_hsa_circ_211165,RMVar_hsa_circ_336781,RMVar_hsa_circ_377144 25999 RMVar_ID_25999 Human_SNP_ID_686616571 A-to-I Human chr20 + 62170933 62170929 62170933 TTTTTGTTTATGTTTTTTTGAGATGGAGTCTCACTCTATCGCCCAGGCTGGAGTGCAGTGATGCG TTTTTGTTTATGTTTTTTTGAGATGGAGT____CTCTATCGCCCAGGCTGGAGTGCAGTGATGCG TCTCA T SS18L1 Ensembl:ENSG00000184402 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1254919624 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_21003,RMVar_hsa_circ_71034,RMVar_hsa_circ_74428 26000 RMVar_ID_26000 Human_SNP_ID_686622246 A-to-I Human chr20 + 62189184 62189184 62189184 TTTAAAAATTAGGCACAGTGGCACTTACCTGTAGCCCCAGCTACTCAGGAGGCTGAGGCAGGAGG TTTAAAAATTAGGCACAGTGGCACTTACCTGTGGCCCCAGCTACTCAGGAGGCTGAGGCAGGAGG A G MTG2 Ensembl:ENSG00000101181 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017989972 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72877 26001 RMVar_ID_26001 Human_SNP_ID_686622304 A-to-I Human chr20 + 62189409 62189409 62189409 ATAGCTCATAGCAGCTTTGAATTCATGGGCTCAAGTGATTCTCCCACCTCAGCCTCCAAAGTAGC ATAGCTCATAGCAGCTTTGAATTCATGGGCTCGAGTGATTCTCCCACCTCAGCCTCCAAAGTAGC A G MTG2 Ensembl:ENSG00000101181 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs948910898 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72877 26002 RMVar_ID_26002 Human_SNP_ID_686625339 A-to-I Human chr20 + 62199368 62199368 62199368 AGCTTTCTGTTTAAAATGTAGCATTGTTGGCCAGGCGTGGTGGCTCACACCTGTAACCCCAGCAC AGCTTTCTGTTTAAAATGTAGCATTGTTGGCCCGGCGTGGTGGCTCACACCTGTAACCCCAGCAC A C MTG2 Ensembl:ENSG00000101181 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1194364093 Functional Loss SNV dbSNP153 33..33 33 - - - 26003 RMVar_ID_26003 Human_SNP_ID_686625545 A-to-I Human chr20 + 62199979 62199979 62199979 GCCCCACCTTGGTCTCCCAAAGTGTTGGGATTACAGGCGTGAGCTACTGCACCTGGCCCTAATTT GCCCCACCTTGGTCTCCCAAAGTGTTGGGATTGCAGGCGTGAGCTACTGCACCTGGCCCTAATTT A G MTG2 Ensembl:ENSG00000101181 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1452648223 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2100912 26004 RMVar_ID_26004 Human_SNP_ID_686644075 A-to-I Human chr20 + 62262015 62262015 62262015 TCCTCAAGTGATCCACCTGCCTCGGCCTCCCAAAGTATTGTGATTAAAGGTAGGAGCCACCATGC TCCTCAAGTGATCCACCTGCCTCGGCCTCCCAGAGTATTGTGATTAAAGGTAGGAGCCACCATGC A G OSBPL2 Ensembl:ENSG00000130703 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs539758410 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7743,RMVar_hsa_circ_273077,RMVar_hsa_circ_327022,RMVar_hsa_circ_296149,RMVar_hsa_circ_117547,RMVar_hsa_circ_60488,RMVar_hsa_circ_211174,RMVar_hsa_circ_211175,RMVar_hsa_circ_211176,RMVar_hsa_circ_211173,RMVar_hsa_circ_80889,RMVar_hsa_circ_346880,RMVar_hsa_circ_24567,RMVar_hsa_circ_211178 26005 RMVar_ID_26005 Human_SNP_ID_686646704 A-to-I Human chr20 + 62271641 62271641 62271641 GCACAGCTAATTTTTGAATTTTTAGTATAGACAGGGTTTCGCTGTGTTGGCCAGACTGGTCTTGA GCACAGCTAATTTTTGAATTTTTAGTATAGACGGGGTTTCGCTGTGTTGGCCAGACTGGTCTTGA A G OSBPL2 Ensembl:ENSG00000130703 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs951870196 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2101178,Human_Splice_Rec_2101179 RMVar_hsa_circ_327022,RMVar_hsa_circ_296149,RMVar_hsa_circ_117547,RMVar_hsa_circ_60488,RMVar_hsa_circ_211175,RMVar_hsa_circ_211176,RMVar_hsa_circ_80889,RMVar_hsa_circ_346880,RMVar_hsa_circ_211178,RMVar_hsa_circ_91956,RMVar_hsa_circ_332661,RMVar_hsa_circ_211179,RMVar_hsa_circ_211180,RMVar_hsa_circ_57507 26006 RMVar_ID_26006 Human_SNP_ID_686647671 A-to-I Human chr20 + 62275169 62275169 62275169 GTTCAGTTACAGTGACCGTGCCACTGAACTCTAACCTGGACTACAGAGCCAGACCGTGTCTCTTT GTTCAGTTACAGTGACCGTGCCACTGAACTCTCACCTGGACTACAGAGCCAGACCGTGTCTCTTT A C OSBPL2 Ensembl:ENSG00000130703 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1408537712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14162030 RMVar_hsa_circ_117547,RMVar_hsa_circ_211176,RMVar_hsa_circ_80889,RMVar_hsa_circ_211178,RMVar_hsa_circ_91956,RMVar_hsa_circ_211180,RMVar_hsa_circ_57507,RMVar_hsa_circ_88991,RMVar_hsa_circ_283682,RMVar_hsa_circ_211182,RMVar_hsa_circ_211183 26007 RMVar_ID_26007 Human_SNP_ID_686657670 A-to-I Human chr20 + 62308181 62308181 62308181 AATACCCTGACCTCGCCCCAGTTCCAGCAGGTAGAGGCCGGGCCCAGGGTGTCCTCCACTGTGTG AATACCCTGACCTCGCCCCAGTTCCAGCAGGTGGAGGCCGGGCCCAGGGTGTCCTCCACTGTGTG A G ADRM1 Ensembl:ENSG00000130706 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs140234397 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5385553,Human_RBP_ID_19006147,Human_RBP_ID_19106950 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_211199,RMVar_hsa_circ_97223,RMVar_hsa_circ_211200 26008 RMVar_ID_26008 Human_SNP_ID_686674335 A-to-I Human chr20 - 62344068 62344068 62344068 GTGATCTTGGCTCGCTACCACTTGTGCCTCCCAGGTTCAAACGATTCTTCTGCTTCAGTCTACCG GTGATCTTGGCTCGCTACCACTTGTGCCTCCCTGGTTCAAACGATTCTTCTGCTTCAGTCTACCG T A LAMA5 Ensembl:ENSG00000130702 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1217914604 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_104880,RMVar_hsa_circ_211232 26009 RMVar_ID_26009 Human_SNP_ID_686674456 A-to-I Human chr20 - 62344502 62344502 62344502 GTGAGCTGAGAACCACCATCACACTCCAGCCTAGGTGACAGAGCGAGACTCCATCTCAAAAAATA GTGAGCTGAGAACCACCATCACACTCCAGCCTGGGTGACAGAGCGAGACTCCATCTCAAAAAATA T C LAMA5 Ensembl:ENSG00000130702 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs957242459 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_104880,RMVar_hsa_circ_211232 26010 RMVar_ID_26010 Human_SNP_ID_686690686 A-to-I Human chr20 - 62389718 62389718 62389718 GCTGCCTCATCAAAAACACTGAATAACCAAGGACTGCTGAGTTTTTCTTCATGGGGGGTCAGCTG GCTGCCTCATCAAAAACACTGAATAACCAAGGGCTGCTGAGTTTTTCTTCATGGGGGGTCAGCTG T C CABLES2 Ensembl:ENSG00000149679 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs375602715 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27299308 Human_miRNA_ID_1329668 RMVar_hsa_circ_91901,RMVar_hsa_circ_108696,RMVar_hsa_circ_211249,RMVar_hsa_circ_211250 26011 RMVar_ID_26011 Human_SNP_ID_686690860 A-to-I Human chr20 - 62390282 62390282 62390282 ATTCTTGGACTCTTGGACCTCTCTGTTCTTCAAGCATCGTGTCACTGTGAAATCCTAACGCCCCT ATTCTTGGACTCTTGGACCTCTCTGTTCTTCAGGCATCGTGTCACTGTGAAATCCTAACGCCCCT T C CABLES2 Ensembl:ENSG00000149679 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1353617577 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14162577,Human_RBP_ID_17396401,Human_RBP_ID_27023919 Human_miRNA_ID_1997043,Human_miRNA_ID_2229536,Human_miRNA_ID_2286796,Human_miRNA_ID_2289795,Human_miRNA_ID_2505506 RMVar_hsa_circ_91901,RMVar_hsa_circ_108696,RMVar_hsa_circ_211249,RMVar_hsa_circ_211250 26012 RMVar_ID_26012 Human_SNP_ID_686813257 A-to-I Human chr20 + 62800154 62800154 62800154 CAAGCCTCTTTCTGCGCTGACTGTGACATTGGAACGTGGCCTTCCTGTCACCCCCTCCGTGCCAC CAAGCCTCTTTCTGCGCTGACTGTGACATTGGCACGTGGCCTTCCTGTCACCCCCTCCGTGCCAC A C MRGBP Ensembl:ENSG00000101189 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1480383643 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_568263,Human_RBP_ID_5119070,Human_RBP_ID_22081755,Human_RBP_ID_27299402,Human_RBP_ID_27488089 Human_miRNA_ID_2878283 RMVar_hsa_circ_86323,RMVar_hsa_circ_105407,RMVar_hsa_circ_96834,RMVar_hsa_circ_211262,RMVar_hsa_circ_211263,RMVar_hsa_circ_89399,RMVar_hsa_circ_211264,RMVar_hsa_circ_211265 26013 RMVar_ID_26013 Human_SNP_ID_686830136 A-to-I Human chr20 - 62846650 62846650 62846650 GTGCTCCTCCTGCCTCAGCCTCCCGAGTAGCTAGGACCGTAGGCGCCCCTCACCACCGCACCCGT GTGCTCCTCCTGCCTCAGCCTCCCGAGTAGCTTGGACCGTAGGCGCCCCTCACCACCGCACCCGT T A TCFL5 Ensembl:ENSG00000101190 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1449701811 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14162770 RMVar_hsa_circ_98382,RMVar_hsa_circ_211267 26014 RMVar_ID_26014 Human_SNP_ID_686832810 A-to-I Human chr20 - 62855703 62855703 62855703 GGAGTGCAATGGCACGATCTCGGTTCAACGCAACCTTCGCCTCCCAGGTTCAAGCGATTCTCCTG GGAGTGCAATGGCACGATCTCGGTTCAACGCAGCCTTCGCCTCCCAGGTTCAAGCGATTCTCCTG T C TCFL5 Ensembl:ENSG00000101190 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985975730 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121977,RMVar_hsa_circ_98382,RMVar_hsa_circ_211267,RMVar_hsa_circ_299367,RMVar_hsa_circ_211268,RMVar_hsa_circ_336077,RMVar_hsa_circ_301656,RMVar_hsa_circ_295276,RMVar_hsa_circ_211273,RMVar_hsa_circ_211274,RMVar_hsa_circ_211272 26015 RMVar_ID_26015 Human_SNP_ID_686832911 A-to-I Human chr20 - 62856064 62856064 62856064 TGTACCTTTTAGTAGAGATGAGGTTTCACCATATTGGCCAGGTTGGTCTCGAACTCCTGACCTTG TGTACCTTTTAGTAGAGATGAGGTTTCACCATGTTGGCCAGGTTGGTCTCGAACTCCTGACCTTG T C TCFL5 Ensembl:ENSG00000101190 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1331411376 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121977,RMVar_hsa_circ_98382,RMVar_hsa_circ_211267,RMVar_hsa_circ_299367,RMVar_hsa_circ_211268,RMVar_hsa_circ_336077,RMVar_hsa_circ_301656,RMVar_hsa_circ_295276,RMVar_hsa_circ_211273,RMVar_hsa_circ_211274,RMVar_hsa_circ_211272 26016 RMVar_ID_26016 Human_SNP_ID_686832946 A-to-I Human chr20 - 62856206 62856206 62856206 CTTTGTCACCCAGGCTGGAATAGTGCAGTGGCATGATCTCGGCTCACTGCAACCTCCGCCTCCCA CTTTGTCACCCAGGCTGGAATAGTGCAGTGGCGTGATCTCGGCTCACTGCAACCTCCGCCTCCCA T C TCFL5 Ensembl:ENSG00000101190 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1325472937 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121977,RMVar_hsa_circ_98382,RMVar_hsa_circ_211267,RMVar_hsa_circ_299367,RMVar_hsa_circ_211268,RMVar_hsa_circ_336077,RMVar_hsa_circ_301656,RMVar_hsa_circ_295276,RMVar_hsa_circ_211273,RMVar_hsa_circ_211274,RMVar_hsa_circ_211272 26017 RMVar_ID_26017 Human_SNP_ID_686850310 A-to-I Human chr20 - 62908232 62908232 62908232 TCACACCTGTCATCCCAGCACTTTGAGAAGTCAAGATGGGAGGATCACTTGAGGCCAAGAGTTCG TCACACCTGTCATCCCAGCACTTTGAGAAGTCGAGATGGGAGGATCACTTGAGGCCAAGAGTTCG T C DIDO1 Ensembl:ENSG00000101191 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs972799991 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25624745 RMVar_hsa_circ_274006,RMVar_hsa_circ_211277,RMVar_hsa_circ_75370,RMVar_hsa_circ_118515,RMVar_hsa_circ_266950,RMVar_hsa_circ_211281,RMVar_hsa_circ_273824,RMVar_hsa_circ_321346,RMVar_hsa_circ_38315,RMVar_hsa_circ_211282,RMVar_hsa_circ_350168 26018 RMVar_ID_26018 Human_SNP_ID_686852591 A-to-I Human chr20 - 62915643 62915643 62915643 AAAAGAATTTTTTTCAAAAATTAGCTGGGCATAGTGGCACGCATCTGTAGTCCCAGTTGCTCATG AAAAGAATTTTTTTCAAAAATTAGCTGGGCATGGTGGCACGCATCTGTAGTCCCAGTTGCTCATG T C DIDO1 Ensembl:ENSG00000101191 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1395700085 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2693284,Human_RBP_ID_14164001 RMVar_hsa_circ_118515,RMVar_hsa_circ_211281 26019 RMVar_ID_26019 Human_SNP_ID_686857334 A-to-I Human chr20 - 62930057 62930057 62930057 TTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGTCAGGCTGGTCTTGAACTCCTAACCT TTTTGTATTTTTAGTAGAGATGGGGTTTCACCGTGTTGGTCAGGCTGGTCTTGAACTCCTAACCT T C DIDO1 Ensembl:ENSG00000101191 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1389405279 Functional Loss SNV dbSNP153 33..33 33 - - - 26020 RMVar_ID_26020 Human_SNP_ID_686857637 A-to-I Human chr20 - 62931134 62931134 62931134 GAGTTCGAGACCAGCCTGGGCAACATAGTGAAACCCCATCTCTACAAAAAATACAAAAACTAGCC GAGTTCGAGACCAGCCTGGGCAACATAGTGAAGCCCCATCTCTACAAAAAATACAAAAACTAGCC T C DIDO1 Ensembl:ENSG00000101191 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1288155098 Functional Loss SNV dbSNP153 33..33 33 - - - 26021 RMVar_ID_26021 Human_SNP_ID_686857849 A-to-I Human chr20 - 62932150 62932150 62932150 TTGGAATGAAAGAGGCAGGGTGGCTCACACCTACAATCCCAGCACTTTGGGGAGGCTGAGACAGG TTGGAATGAAAGAGGCAGGGTGGCTCACACCTGCAATCCCAGCACTTTGGGGAGGCTGAGACAGG T C DIDO1 Ensembl:ENSG00000101191 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs949704193 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571307 26022 RMVar_ID_26022 Human_SNP_ID_686857873 A-to-I Human chr20 - 62932234 62932233 62932234 CTCTCCTGGGCCTCCCAAAGTGTCAGGATTACAGGCGTGAGCCACCGTGCCTGGCCCTACATTTA CTCTCCTGGGCCTCCCAAAGTGTCAGGATTAC_GGCGTGAGCCACCGTGCCTGGCCCTACATTTA CT C DIDO1 Ensembl:ENSG00000101191 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1485066101 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_17571768 26023 RMVar_ID_26023 Human_SNP_ID_686857879 A-to-I Human chr20 - 62932248 62932248 62932248 GCTCAAGTGATCCTCTCTCCTGGGCCTCCCAAAGTGTCAGGATTACAGGCGTGAGCCACCGTGCC GCTCAAGTGATCCTCTCTCCTGGGCCTCCCAACGTGTCAGGATTACAGGCGTGAGCCACCGTGCC T G DIDO1 Ensembl:ENSG00000101191 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs903761259 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571768 26024 RMVar_ID_26024 Human_SNP_ID_686857893 A-to-I Human chr20 - 62932301 62932301 62932301 TAGAAGTAGAAATAAGAGTTCCTATGTTTCCCAGGCTGGCCTTCAACTCCTGGGCTCAAGTGATC TAGAAGTAGAAATAAGAGTTCCTATGTTTCCCCGGCTGGCCTTCAACTCCTGGGCTCAAGTGATC T G DIDO1 Ensembl:ENSG00000101191 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1396436519 Functional Loss SNV dbSNP153 33..33 33 - - - 26025 RMVar_ID_26025 Human_SNP_ID_686858229 A-to-I Human chr20 - 62933687 62933687 62933687 TTGTTTATTTTTTGTAGAGGAGAGGTCTCACTATGTTGCCCAGGCTGTTCTCAAACTTCTGCGTG TTGTTTATTTTTTGTAGAGGAGAGGTCTCACTGTGTTGCCCAGGCTGTTCTCAAACTTCTGCGTG T C DIDO1 Ensembl:ENSG00000101191 Protein coding intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs535445876 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7019535,Human_RBP_ID_14164657 26026 RMVar_ID_26026 Human_SNP_ID_686858263 A-to-I Human chr20 - 62933826 62933826 62933826 AGGGGAGAGCAGTTTGCCCAGGCTGGAGTGCAATGGTGTGATAATGGCTCACTGCAACCTACACC AGGGGAGAGCAGTTTGCCCAGGCTGGAGTGCAGTGGTGTGATAATGGCTCACTGCAACCTACACC T C DIDO1 Ensembl:ENSG00000101191 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1236829826 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14164666 26027 RMVar_ID_26027 Human_SNP_ID_686937353 A-to-I Human chr20 - 63205637 63205637 63205637 GGGTGTGGTGGTGGGTGTCTGTAATCCCAGCTACTTGGGAGGCTGAGGCATGAGAATCGCTTGAA GGGTGTGGTGGTGGGTGTCTGTAATCCCAGCTTCTTGGGAGGCTGAGGCATGAGAATCGCTTGAA T A YTHDF1 Ensembl:ENSG00000149658 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs752394426 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2087309 RMVar_hsa_circ_10365,RMVar_hsa_circ_113462,RMVar_hsa_circ_211294,RMVar_hsa_circ_112497,RMVar_hsa_circ_109550,RMVar_hsa_circ_211297,RMVar_hsa_circ_211298 26028 RMVar_ID_26028 Human_SNP_ID_686937358 A-to-I Human chr20 - 63205647 63205647 63205647 AAAATTAACCGGGTGTGGTGGTGGGTGTCTGTAATCCCAGCTACTTGGGAGGCTGAGGCATGAGA AAAATTAACCGGGTGTGGTGGTGGGTGTCTGTGATCCCAGCTACTTGGGAGGCTGAGGCATGAGA T C YTHDF1 Ensembl:ENSG00000149658 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1436222419 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2087309 RMVar_hsa_circ_10365,RMVar_hsa_circ_113462,RMVar_hsa_circ_211294,RMVar_hsa_circ_112497,RMVar_hsa_circ_109550,RMVar_hsa_circ_211297,RMVar_hsa_circ_211298 26029 RMVar_ID_26029 Human_SNP_ID_686937770 A-to-I Human chr20 - 63207234 63207234 63207234 TTGATCTCCTGACCTTGTGATCCGTCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAG TTGATCTCCTGACCTTGTGATCCGTCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAG T C YTHDF1 Ensembl:ENSG00000149658 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1398696008 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10365,RMVar_hsa_circ_113462,RMVar_hsa_circ_211294,RMVar_hsa_circ_112497,RMVar_hsa_circ_109550,RMVar_hsa_circ_211297,RMVar_hsa_circ_211298 26030 RMVar_ID_26030 Human_SNP_ID_686937993 A-to-I Human chr20 - 63207808 63207808 63207808 TAGAGACGGGGTTTAACCATATTGATCAGACTAGTCTCGAACTCCTGACCTTGTGATTCACCTGC TAGAGACGGGGTTTAACCATATTGATCAGACTTGTCTCGAACTCCTGACCTTGTGATTCACCTGC T A YTHDF1 Ensembl:ENSG00000149658 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1237566518 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2693485,Human_RBP_ID_14165879,Human_RBP_ID_25624934 RMVar_hsa_circ_10365,RMVar_hsa_circ_113462,RMVar_hsa_circ_211294,RMVar_hsa_circ_112497,RMVar_hsa_circ_109550,RMVar_hsa_circ_211297,RMVar_hsa_circ_211298 26031 RMVar_ID_26031 Human_SNP_ID_687032203 A-to-I Human chr20 - 63490280 63490280 63490280 CGGGCAGATCACGAGGTCAAGAGATCAAGTCCATCCTGGTCAACATGGTGAAACCCCGTCTCTAC CGGGCAGATCACGAGGTCAAGAGATCAAGTCCCTCCTGGTCAACATGGTGAAACCCCGTCTCTAC T G EEF1A2 Ensembl:ENSG00000101210 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1385557073 Functional Loss SNV dbSNP153 33..33 33 - - - 26032 RMVar_ID_26032 Human_SNP_ID_687069283 A-to-I Human chr20 - 63597311 63597311 63597311 AAAAATAAAAAAAAAATTATCTGGATTTGGTGACATATGCCTGTGGTCCCAGCTGCTCGAGAGGC AAAAATAAAAAAAAAATTATCTGGATTTGGTGTCATATGCCTGTGGTCCCAGCTGCTCGAGAGGC T A GMEB2 Ensembl:ENSG00000101216 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs413393 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2585,GWAS_ID_2586,GWAS_ID_2587,GWAS_ID_2588,GWAS_ID_2589 RMVar_hsa_circ_46540,RMVar_hsa_circ_101160,RMVar_hsa_circ_211325,RMVar_hsa_circ_31407 26033 RMVar_ID_26033 Human_SNP_ID_687069284 A-to-I Human chr20 - 63597311 63597311 63597311 AAAAATAAAAAAAAAATTATCTGGATTTGGTGACATATGCCTGTGGTCCCAGCTGCTCGAGAGGC AAAAATAAAAAAAAAATTATCTGGATTTGGTGGCATATGCCTGTGGTCCCAGCTGCTCGAGAGGC T C GMEB2 Ensembl:ENSG00000101216 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs413393 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2585,GWAS_ID_2586,GWAS_ID_2587,GWAS_ID_2588,GWAS_ID_2589 RMVar_hsa_circ_46540,RMVar_hsa_circ_101160,RMVar_hsa_circ_211325,RMVar_hsa_circ_31407 26034 RMVar_ID_26034 Human_SNP_ID_687077787 A-to-I Human chr20 - 63625776 63625776 63625776 CTGGCTAACACGGTGAAACCCTGTCTCTACTAAAAATACAAAAGTTAGCCGGGCGTGGTGGTGTG CTGGCTAACACGGTGAAACCCTGTCTCTACTACAAATACAAAAGTTAGCCGGGCGTGGTGGTGTG T G GMEB2 Ensembl:ENSG00000101216 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1038247167 Functional Loss SNV dbSNP153 33..33 33 - - - 26035 RMVar_ID_26035 Human_SNP_ID_687093734 A-to-I Human chr20 + 63673462 63673461 63673463 AGTGAAATAATTGTTTGTTTGTTTGTTGAGACAGGGTCTCCTTCTGTCGTCCAGGCTGGAGTTCA AGTGAAATAATTGTTTGTTTGTTTGTTGAGAC__GGTCTCCTTCTGTCGTCCAGGCTGGAGTTCA CAG C RTEL1-TNFRSF6B,RTEL1 Ensembl:ENSG00000026036,Ensembl:ENSG00000258366 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1329334654 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_6246,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_282420,RMVar_hsa_circ_211333,RMVar_hsa_circ_348649,RMVar_hsa_circ_317360,RMVar_hsa_circ_43156,RMVar_hsa_circ_211334 26036 RMVar_ID_26036 Human_SNP_ID_687094567 A-to-I Human chr20 + 63676100 63676100 63676100 CTGTTCCCCCACCCCTTTGGAGATGGGGTCTCACTCTGTCACCCAGGCTGGAGAGCGGTGGTGCC CTGTTCCCCCACCCCTTTGGAGATGGGGTCTCTCTCTGTCACCCAGGCTGGAGAGCGGTGGTGCC A T RTEL1-TNFRSF6B,RTEL1 Ensembl:ENSG00000026036,Ensembl:ENSG00000258366 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs539913105 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6246,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 26037 RMVar_ID_26037 Human_SNP_ID_687094745 A-to-I Human chr20 + 63676674 63676674 63676674 ATGCTGGGGGTGGGCCGGGTGTGCTGTCTCACACCTGTCATCCCAGCACTTTGGGAGGCCCAGGC ATGCTGGGGGTGGGCCGGGTGTGCTGTCTCACGCCTGTCATCCCAGCACTTTGGGAGGCCCAGGC A G RTEL1-TNFRSF6B,RTEL1 Ensembl:ENSG00000026036,Ensembl:ENSG00000258366 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1186402529 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6246,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 26038 RMVar_ID_26038 Human_SNP_ID_687109552 A-to-I Human chr20 + 63709526 63709526 63709526 GGTCGTGGTGGCGCGCACCTGTGGTCCTGGCTACTCAGGAGGCTGAGGCAGGAGAATTGGTTGAA GGTCGTGGTGGCGCGCACCTGTGGTCCTGGCTGCTCAGGAGGCTGAGGCAGGAGAATTGGTTGAA A G AL121845.3,ZGPAT Ensembl:ENSG00000273154,Ensembl:ENSG00000197114 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs986083723 Functional Loss SNV dbSNP153 33..33 33 - - - 26039 RMVar_ID_26039 Human_SNP_ID_687110162 A-to-I Human chr20 + 63711171 63711171 63711171 CCCACCTCAGCCTCCCTAATAGCTGATACTACAAGTGTGCACTGCCACGCCCAGCTAATTTTTGT CCCACCTCAGCCTCCCTAATAGCTGATACTACGAGTGTGCACTGCCACGCCCAGCTAATTTTTGT A G AL121845.3,ZGPAT Ensembl:ENSG00000273154,Ensembl:ENSG00000197114 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1441263172 Functional Loss SNV dbSNP153 33..33 33 - - - 26040 RMVar_ID_26040 Human_SNP_ID_687110643 A-to-I Human chr20 + 63712878 63712877 63712879 AGATCATGCCACTGCACTCCAGCCTGGGTAACAGAGGGAGACTCCATCTTAAACAACAACAATAA AGATCATGCCACTGCACTCCAGCCTGGGTAAC__AGGGAGACTCCATCTTAAACAACAACAATAA CAG C AL121845.3,ZGPAT Ensembl:ENSG00000273154,Ensembl:ENSG00000197114 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1012397210 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_22723025 26041 RMVar_ID_26041 Human_SNP_ID_687111053 A-to-I Human chr20 + 63714305 63714305 63714305 AAAATTAGCTGGGTGAGGTGATGTGCACCTGTAGTCCCAGCTACTTGAGAGGGTGAGACATGAGA AAAATTAGCTGGGTGAGGTGATGTGCACCTGTCGTCCCAGCTACTTGAGAGGGTGAGACATGAGA A C AL121845.3,ZGPAT Ensembl:ENSG00000273154,Ensembl:ENSG00000197114 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs956112227 Functional Loss SNV dbSNP153 33..33 33 - - - 26042 RMVar_ID_26042 Human_SNP_ID_687111071 A-to-I Human chr20 + 63714381 63714381 63714381 CTGGGGGGCGGAGGTTGCAGTGAGCCAAGATCATGCCACTCCACTCCAGCCTGGACGACAGAGCA CTGGGGGGCGGAGGTTGCAGTGAGCCAAGATCGTGCCACTCCACTCCAGCCTGGACGACAGAGCA A G AL121845.3,ZGPAT Ensembl:ENSG00000273154,Ensembl:ENSG00000197114 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968321348 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23311717 26043 RMVar_ID_26043 Human_SNP_ID_687111149 A-to-I Human chr20 + 63714660 63714660 63714660 TTTTATCATGAAAGGGTGTTGATTTTTTTTTTAAAGATAGGGTCTTGTTCTGTCACCCAGGCTGG TTTTATCATGAAAGGGTGTTGATTTTTTTTTTGAAGATAGGGTCTTGTTCTGTCACCCAGGCTGG A G AL121845.3,ZGPAT Ensembl:ENSG00000273154,Ensembl:ENSG00000197114 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569735662 Functional Loss SNV dbSNP153 33..33 33 - - - 26044 RMVar_ID_26044 Human_SNP_ID_687111196 A-to-I Human chr20 + 63714833 63714833 63714833 CCCAGCTAATTTTTTAATTTTTCTGTAGAGGTAGGGTCCTGCTTTGCTGCCCAGGCTGGTCTTAA CCCAGCTAATTTTTTAATTTTTCTGTAGAGGTGGGGTCCTGCTTTGCTGCCCAGGCTGGTCTTAA A G AL121845.3,ZGPAT Ensembl:ENSG00000273154,Ensembl:ENSG00000197114 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1449055467 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14167859,Human_RBP_ID_22260927 26045 RMVar_ID_26045 Human_SNP_ID_687111772 A-to-I Human chr20 + 63716785 63716785 63716785 CTCATTGCAACCTCCGACTCCCAGATTCCAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGA CTCATTGCAACCTCCGACTCCCAGATTCCAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGA A G AL121845.3,ZGPAT Ensembl:ENSG00000273154,Ensembl:ENSG00000197114 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs991473464 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14167929 26046 RMVar_ID_26046 Human_SNP_ID_687112750 A-to-I Human chr20 + 63720581 63720581 63720581 TTAAGTGAGTCTCCCACCTTAGTCTCCTGAGTAGCTAGAACTACAAGCATGTGCCACCATGCCTG TTAAGTGAGTCTCCCACCTTAGTCTCCTGAGTGGCTAGAACTACAAGCATGTGCCACCATGCCTG A G AL121845.3,ZGPAT Ensembl:ENSG00000273154,Ensembl:ENSG00000197114 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1172599978 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14168014 26047 RMVar_ID_26047 Human_SNP_ID_687113891 A-to-I Human chr20 + 63724808 63724808 63724808 TGATTTTCCTGCCTCAGCCTCCCAAGTAGCTGAGACTGCAGGCACCTGCCACCACCCCCAGCCAA TGATTTTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTGCAGGCACCTGCCACCACCCCCAGCCAA A G AL121845.3,ZGPAT Ensembl:ENSG00000273154,Ensembl:ENSG00000197114 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1409096453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14168097 26048 RMVar_ID_26048 Human_SNP_ID_687114676 A-to-I Human chr20 + 63727407 63727407 63727407 GGGAGTACAGGCTCATGACACCACGCCTGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCT GGGAGTACAGGCTCATGACACCACGCCTGGCTGATTTTTGTATTTTTAGTAGAGACGGGGTTTCT A G AL121845.3,ZGPAT Ensembl:ENSG00000273154,Ensembl:ENSG00000197114 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs902970887 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25631844 26049 RMVar_ID_26049 Human_SNP_ID_687137630 A-to-I Human chr20 - 63793712 63793712 63793712 GTGAACCGTTGTGAGGTAGCCGCTGCTTCTATAAAATCTTACGTGGAGGTGTGGACCGTTGTGAG GTGAACCGTTGTGAGGTAGCCGCTGCTTCTATGAAATCTTACGTGGAGGTGTGGACCGTTGTGAG T C ZBTB46 Ensembl:ENSG00000130584 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs6062531 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17143372 26050 RMVar_ID_26050 Human_SNP_ID_687137631 A-to-I Human chr20 - 63793714 63793712 63793714 ATGTGAACCGTTGTGAGGTAGCCGCTGCTTCTATAAAATCTTACGTGGAGGTGTGGACCGTTGTG ATGTGAACCGTTGTGAGGTAGCCGCTGCTTCTGTGAAATCTTACGTGGAGGTGTGGACCGTTGTG TAT CAC ZBTB46 Ensembl:ENSG00000130584 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs386816188 Functional Loss MNV dbSNP153 33..35 33 - - - Human_RBP_ID_17143372 26051 RMVar_ID_26051 Human_SNP_ID_687137631 A-to-I Human chr20 - 63793712 63793712 63793714 GTGAACCGTTGTGAGGTAGCCGCTGCTTCTATAAAATCTTACGTGGAGGTGTGGACCGTTGTGAG GTGAACCGTTGTGAGGTAGCCGCTGCTTCTGTGAAATCTTACGTGGAGGTGTGGACCGTTGTGAG TAT CAC ZBTB46 Ensembl:ENSG00000130584 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs386816188 Functional Loss MNV dbSNP153 31..33 33 - - - Human_RBP_ID_17143372 26052 RMVar_ID_26052 Human_SNP_ID_687137632 A-to-I Human chr20 - 63793714 63793714 63793714 ATGTGAACCGTTGTGAGGTAGCCGCTGCTTCTATAAAATCTTACGTGGAGGTGTGGACCGTTGTG ATGTGAACCGTTGTGAGGTAGCCGCTGCTTCTGTAAAATCTTACGTGGAGGTGTGGACCGTTGTG T C ZBTB46 Ensembl:ENSG00000130584 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs6062532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17143372 26053 RMVar_ID_26053 Human_SNP_ID_687162407 A-to-I Human chr20 + 63871243 63871243 63871243 TTTTGTATTTTTAGTAGAGACAGAGTTTCACCATGTTGGCCAGGCTGGTCCCGAACTCCGAGTCT TTTTGTATTTTTAGTAGAGACAGAGTTTCACCGTGTTGGCCAGGCTGGTCCCGAACTCCGAGTCT A G TPD52L2 Ensembl:ENSG00000101150 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968279414 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14168596,Human_RBP_ID_25625413 RMVar_hsa_circ_100901,RMVar_hsa_circ_351807,RMVar_hsa_circ_211345,RMVar_hsa_circ_307759,RMVar_hsa_circ_211346 26054 RMVar_ID_26054 Human_SNP_ID_687162408 A-to-I Human chr20 + 63871243 63871243 63871243 TTTTGTATTTTTAGTAGAGACAGAGTTTCACCATGTTGGCCAGGCTGGTCCCGAACTCCGAGTCT TTTTGTATTTTTAGTAGAGACAGAGTTTCACCTTGTTGGCCAGGCTGGTCCCGAACTCCGAGTCT A T TPD52L2 Ensembl:ENSG00000101150 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968279414 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14168596,Human_RBP_ID_25625413 RMVar_hsa_circ_100901,RMVar_hsa_circ_351807,RMVar_hsa_circ_211345,RMVar_hsa_circ_307759,RMVar_hsa_circ_211346 26055 RMVar_ID_26055 Human_SNP_ID_687164499 A-to-I Human chr20 + 63877350 63877349 63877351 CCCGGCTAATTTTTTGTATTTTTAGTAGAGACAGGGTTTCATGGTGTTAGCCAGGATGGTTTCGA CCCGGCTAATTTTTTGTATTTTTAGTAGAGAC__GGTTTCATGGTGTTAGCCAGGATGGTTTCGA CAG C TPD52L2 Ensembl:ENSG00000101150 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1336402831 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_22593,RMVar_hsa_circ_53232 26056 RMVar_ID_26056 Human_SNP_ID_687165326 A-to-I Human chr20 + 63880629 63880629 63880629 TTTGTATTTTTGGGCTGGGCACGGTGGCTCACACCTGTAATCCCAACACTTTTGGAGGCTGAGGC TTTGTATTTTTGGGCTGGGCACGGTGGCTCACGCCTGTAATCCCAACACTTTTGGAGGCTGAGGC A G TPD52L2 Ensembl:ENSG00000101150 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs73611735 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22593,RMVar_hsa_circ_53232 26057 RMVar_ID_26057 Human_SNP_ID_687165379 A-to-I Human chr20 + 63880823 63880823 63880823 TGAGGCAGGAGAATGGCGTGCACCCGTGAGGCAGAGCTTGCAGTGAGCCGAGATGGTGCTGCTGC TGAGGCAGGAGAATGGCGTGCACCCGTGAGGCGGAGCTTGCAGTGAGCCGAGATGGTGCTGCTGC A G TPD52L2 Ensembl:ENSG00000101150 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs967617577 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25625441 RMVar_hsa_circ_22593,RMVar_hsa_circ_53232 26058 RMVar_ID_26058 Human_SNP_ID_687165517 A-to-I Human chr20 + 63881250 63881250 63881250 GGGCGTGGTGGTGGGTGCCTGTAATCCCAGCTACTTGGGACGCTGAGGCAGGAGAATCTCTTGAA GGGCGTGGTGGTGGGTGCCTGTAATCCCAGCTCCTTGGGACGCTGAGGCAGGAGAATCTCTTGAA A C TPD52L2 Ensembl:ENSG00000101150 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs905414929 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22593,RMVar_hsa_circ_53232 26059 RMVar_ID_26059 Human_SNP_ID_687171144 A-to-I Human chr20 + 63899788 63899788 63899788 TATTTTTAGTAGAGACAGGGTTTCGCGGTGTTAGCCAGGATGGTCTCGATCTCCTGACCTTGTGA TATTTTTAGTAGAGACAGGGTTTCGCGGTGTTCGCCAGGATGGTCTCGATCTCCTGACCTTGTGA A C DNAJC5 Ensembl:ENSG00000101152 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs530787084 Functional Loss SNV dbSNP153 33..33 33 - - - 26060 RMVar_ID_26060 Human_SNP_ID_687171145 A-to-I Human chr20 + 63899788 63899788 63899788 TATTTTTAGTAGAGACAGGGTTTCGCGGTGTTAGCCAGGATGGTCTCGATCTCCTGACCTTGTGA TATTTTTAGTAGAGACAGGGTTTCGCGGTGTTGGCCAGGATGGTCTCGATCTCCTGACCTTGTGA A G DNAJC5 Ensembl:ENSG00000101152 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs530787084 Functional Loss SNV dbSNP153 33..33 33 - - - 26061 RMVar_ID_26061 Human_SNP_ID_687171146 A-to-I Human chr20 + 63899788 63899788 63899788 TATTTTTAGTAGAGACAGGGTTTCGCGGTGTTAGCCAGGATGGTCTCGATCTCCTGACCTTGTGA TATTTTTAGTAGAGACAGGGTTTCGCGGTGTTTGCCAGGATGGTCTCGATCTCCTGACCTTGTGA A T DNAJC5 Ensembl:ENSG00000101152 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs530787084 Functional Loss SNV dbSNP153 33..33 33 - - - 26062 RMVar_ID_26062 Human_SNP_ID_687172369 A-to-I Human chr20 + 63903489 63903489 63903489 GCCACTACGCCCGGCTGATTTTTGTATTTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGA GCCACTACGCCCGGCTGATTTTTGTATTTTTTGGTAGAGACGGGGTTTCACCATGTTGGCCAGGA A G DNAJC5 Ensembl:ENSG00000101152 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs932827725 Functional Loss SNV dbSNP153 33..33 33 - - - 26063 RMVar_ID_26063 Human_SNP_ID_687172403 A-to-I Human chr20 + 63903581 63903581 63903581 TGCGCACCTTGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACTGCGCTCGGCCCATCTCA TGCGCACCTTGGCCTCCCAAAGTGCTGGGATTGCAGGTGTGAGCCACTGCGCTCGGCCCATCTCA A G DNAJC5 Ensembl:ENSG00000101152 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1458675731 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23184986 26064 RMVar_ID_26064 Human_SNP_ID_687172438 A-to-I Human chr20 + 63903672 63903672 63903672 AAATTTTTAAAAAATTAAAAACATTTTTGGCCAGGCTTAGTGGTTTAAGCCTGTAATCCCAGTGC AAATTTTTAAAAAATTAAAAACATTTTTGGCCCGGCTTAGTGGTTTAAGCCTGTAATCCCAGTGC A C DNAJC5 Ensembl:ENSG00000101152 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1051261645 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14173909 26065 RMVar_ID_26065 Human_SNP_ID_687172468 A-to-I Human chr20 + 63903814 63903814 63903814 TCTACTAAAAATACAAAAATTTGGGCAGGTGCAGTGGCTGACACCTGTAACCCCAACACTTTGGG TCTACTAAAAATACAAAAATTTGGGCAGGTGCTGTGGCTGACACCTGTAACCCCAACACTTTGGG A T DNAJC5 Ensembl:ENSG00000101152 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1454548785 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571781 26066 RMVar_ID_26066 Human_SNP_ID_687173220 A-to-I Human chr20 + 63906326 63906326 63906326 CTGGCCAACATGGCGAAACCCCTTCCATCTCTACTAAAAATATGAAAATTAGCCAGGTGTGGTGC CTGGCCAACATGGCGAAACCCCTTCCATCTCTTCTAAAAATATGAAAATTAGCCAGGTGTGGTGC A T DNAJC5 Ensembl:ENSG00000101152 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs773192174 Functional Loss SNV dbSNP153 33..33 33 - - - 26067 RMVar_ID_26067 Human_SNP_ID_687174542 A-to-I Human chr20 + 63910905 63910905 63910905 ATGTTGGCCAGGCTGGTCTATCTCCTGACCTCATGATCCGCCTGCCTTGGCCTCCCAAAGTACTG ATGTTGGCCAGGCTGGTCTATCTCCTGACCTCGTGATCCGCCTGCCTTGGCCTCCCAAAGTACTG A G DNAJC5 Ensembl:ENSG00000101152 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs201499311 Functional Loss SNV dbSNP153 33..33 33 - - - 26068 RMVar_ID_26068 Human_SNP_ID_687174879 A-to-I Human chr20 + 63912121 63912121 63912121 GGCCGGGAGTTTGAGTCCAACCTGGCCAATATAGCAAAACCTCATCTCTGCTAACAATACAAAAA GGCCGGGAGTTTGAGTCCAACCTGGCCAATATGGCAAAACCTCATCTCTGCTAACAATACAAAAA A G DNAJC5 Ensembl:ENSG00000101152 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900456567 Functional Loss SNV dbSNP153 33..33 33 - - - 26069 RMVar_ID_26069 Human_SNP_ID_687178031 A-to-I Human chr20 + 63922031 63922031 63922031 AAACTCTTGATCTCAGGTGATTCAACCACCTCAGCCTCCCAAAGTGCTGGAATTACAGGCGTGAG AAACTCTTGATCTCAGGTGATTCAACCACCTCCGCCTCCCAAAGTGCTGGAATTACAGGCGTGAG A C DNAJC5 Ensembl:ENSG00000101152 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924614456 Functional Loss SNV dbSNP153 33..33 33 - - - 26070 RMVar_ID_26070 Human_SNP_ID_687178110 A-to-I Human chr20 + 63922278 63922278 63922278 GAGGTCAGGAGTTCAAGACTATCCTGGCCAACATGGTGAAGCCCATCTGTACTAAAAATACAAAA GAGGTCAGGAGTTCAAGACTATCCTGGCCAACGTGGTGAAGCCCATCTGTACTAAAAATACAAAA A G DNAJC5 Ensembl:ENSG00000101152 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1193851382 Functional Loss SNV dbSNP153 33..33 33 - - - 26071 RMVar_ID_26071 Human_SNP_ID_687178187 A-to-I Human chr20 + 63922570 63922570 63922570 AAGGCAGGAGGATCACTTGAGCCAAGGAATTCAAGATCAGCCTGAGCAACATAGACCCCGTCTCT AAGGCAGGAGGATCACTTGAGCCAAGGAATTCGAGATCAGCCTGAGCAACATAGACCCCGTCTCT A G DNAJC5 Ensembl:ENSG00000101152 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs137953881 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14170144 26072 RMVar_ID_26072 Human_SNP_ID_687178391 A-to-I Human chr20 + 63923303 63923302 63923303 GTCTCTATAGAAAATTTTAAAGTTAGCTGGGCATGGTGGCACATTCCTGTAGTCTTAGCTGCTTG GTCTCTATAGAAAATTTTAAAGTTAGCTGGGC_TGGTGGCACATTCCTGTAGTCTTAGCTGCTTG CA C DNAJC5 Ensembl:ENSG00000101152 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1016392583 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5132711,Human_RBP_ID_14170155,Human_RBP_ID_22479246 26073 RMVar_ID_26073 Human_SNP_ID_687178397 A-to-I Human chr20 + 63923321 63923321 63923321 AAAGTTAGCTGGGCATGGTGGCACATTCCTGTAGTCTTAGCTGCTTGGGATGCTGAGAAGGGAGG AAAGTTAGCTGGGCATGGTGGCACATTCCTGTGGTCTTAGCTGCTTGGGATGCTGAGAAGGGAGG A G DNAJC5 Ensembl:ENSG00000101152 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs963547106 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5132711,Human_RBP_ID_17571996,Human_RBP_ID_22478953 26074 RMVar_ID_26074 Human_SNP_ID_687178945 A-to-I Human chr20 + 63925212 63925212 63925212 CAGTGTAGAAAACCAATTATAAGAGGCCGGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTA CAGTGTAGAAAACCAATTATAAGAGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTA A G DNAJC5 Ensembl:ENSG00000101152 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1228988043 Functional Loss SNV dbSNP153 33..33 33 - - - 26075 RMVar_ID_26075 Human_SNP_ID_687179034 A-to-I Human chr20 + 63925438 63925438 63925438 CCGGGAGGCAGAGATTGCAGTGAACTGAGGTCACACCACTGCACTCCAGCCTGGGCAAACAGAGC CCGGGAGGCAGAGATTGCAGTGAACTGAGGTCGCACCACTGCACTCCAGCCTGGGCAAACAGAGC A G DNAJC5 Ensembl:ENSG00000101152 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1447343973 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23004567,Human_RBP_ID_25625704 26076 RMVar_ID_26076 Human_SNP_ID_687179050 A-to-I Human chr20 + 63925466 63925465 63925467 GGTCACACCACTGCACTCCAGCCTGGGCAAACAGAGCGAGACTCCACCTCAAAAATAAAAATTAG GGTCACACCACTGCACTCCAGCCTGGGCAAAC__AGCGAGACTCCACCTCAAAAATAAAAATTAG CAG C DNAJC5 Ensembl:ENSG00000101152 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1213648099 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_25625707 26077 RMVar_ID_26077 Human_SNP_ID_687179273 A-to-I Human chr20 + 63926004 63926004 63926004 TGCCTGCCACCACTTCCGGCTAATTTTTTTGTATTTTTATTAGAGATGGGGTTTCACTGTGTTAG TGCCTGCCACCACTTCCGGCTAATTTTTTTGTGTTTTTATTAGAGATGGGGTTTCACTGTGTTAG A G DNAJC5 Ensembl:ENSG00000101152 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037086072 Functional Loss SNV dbSNP153 33..33 33 - - - 26078 RMVar_ID_26078 Human_SNP_ID_687179960 A-to-I Human chr20 + 63928423 63928423 63928423 TTGTACCACGTCCTTGGGTTGGACAAGAACGCAACCTCAGATGACATTAAAAAGTCCTATCGGTA TTGTACCACGTCCTTGGGTTGGACAAGAACGCCACCTCAGATGACATTAAAAAGTCCTATCGGTA A C DNAJC5 Ensembl:ENSG00000101152 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1171411674 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1600880,Human_RBP_ID_1933028,Human_RBP_ID_4660649,Human_RBP_ID_14170301 Human_Splice_Rec_2105264,Human_Splice_Rec_2105265,Human_Splice_Rec_2105272,Human_Splice_Rec_2105273 Human_miRNA_ID_2404635 RMVar_hsa_circ_79675,RMVar_hsa_circ_274642,RMVar_hsa_circ_287776,RMVar_hsa_circ_274501,RMVar_hsa_circ_211350,RMVar_hsa_circ_211351,RMVar_hsa_circ_211352,RMVar_hsa_circ_211349 26079 RMVar_ID_26079 Human_SNP_ID_687202096 A-to-I Human chr20 + 63994616 63994616 63994616 AGCCTTGGGGAGAACCTGTCTTTACAAAAAATAAAAACTTAGCCAGGCATGGTGGCCCACGCTTG AGCCTTGGGGAGAACCTGTCTTTACAAAAAATGAAAACTTAGCCAGGCATGGTGGCCCACGCTTG A G PRPF6 Ensembl:ENSG00000101161 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs989282019 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123569,RMVar_hsa_circ_269558,RMVar_hsa_circ_74273,RMVar_hsa_circ_211371,RMVar_hsa_circ_77707,RMVar_hsa_circ_120096,RMVar_hsa_circ_211372,RMVar_hsa_circ_211373,RMVar_hsa_circ_351826 26080 RMVar_ID_26080 Human_SNP_ID_687202599 A-to-I Human chr20 + 63996245 63996245 63996245 CCTGTAATCCCAGCTACTTGGGAGGCTAAGGCAGGAGAATTGCTTGAACCCGGGCGTTGGAGGTT CCTGTAATCCCAGCTACTTGGGAGGCTAAGGCCGGAGAATTGCTTGAACCCGGGCGTTGGAGGTT A C PRPF6 Ensembl:ENSG00000101161 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1435827926 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45960,RMVar_hsa_circ_123569,RMVar_hsa_circ_269558,RMVar_hsa_circ_211371,RMVar_hsa_circ_77707,RMVar_hsa_circ_120096,RMVar_hsa_circ_211372,RMVar_hsa_circ_211373,RMVar_hsa_circ_88388,RMVar_hsa_circ_351826,RMVar_hsa_circ_211374,RMVar_hsa_circ_211375 26081 RMVar_ID_26081 Human_SNP_ID_687279349 A-to-I Human chr20 + 64260946 64260946 64260946 AAACTCCTGGGCGCCAGCTCTCCACCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAG AAACTCCTGGGCGCCAGCTCTCCACCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAG A G PCMTD2 Ensembl:ENSG00000203880 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1294996266 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_211406,RMVar_hsa_circ_115537,RMVar_hsa_circ_211407,RMVar_hsa_circ_69792 26082 RMVar_ID_26082 Human_SNP_ID_479039659 A-to-I Human chr11 + 100337209 100337209 100337209 GACACAGATGACACCAGCAGTGAAAACACTGTAGTTCCTCCAGAAACATATGTGAAAGTGGCAGG GACACAGATGACACCAGCAGTGAAAACACTGTGGTTCCTCCAGAAACATATGTGAAAGTGGCAGG A G RPA2P3,CNTN5 Ensembl:ENSG00000255547,Ensembl:ENSG00000149972 Pseudogene,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878874454 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1827262,Human_miRNA_ID_1887559,Human_miRNA_ID_1909039 RMVar_hsa_circ_23698 26083 RMVar_ID_26083 Human_SNP_ID_479138140 A-to-I Human chr11 + 100698091 100698091 100698091 AAATTAATTATTTGTAGAGATAGGATCTTGCTATGCTTCCTTGGCTTGTCTCCAACTTCTAGCCT AAATTAATTATTTGTAGAGATAGGATCTTGCTCTGCTTCCTTGGCTTGTCTCCAACTTCTAGCCT A C ARHGAP42 Ensembl:ENSG00000165895 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs921991654 Functional Loss SNV dbSNP153 33..33 33 - - - 26084 RMVar_ID_26084 Human_SNP_ID_479138141 A-to-I Human chr11 + 100698091 100698091 100698091 AAATTAATTATTTGTAGAGATAGGATCTTGCTATGCTTCCTTGGCTTGTCTCCAACTTCTAGCCT AAATTAATTATTTGTAGAGATAGGATCTTGCTGTGCTTCCTTGGCTTGTCTCCAACTTCTAGCCT A G ARHGAP42 Ensembl:ENSG00000165895 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs921991654 Functional Loss SNV dbSNP153 33..33 33 - - - 26085 RMVar_ID_26085 Human_SNP_ID_479140922 A-to-I Human chr11 + 100709059 100709054 100709059 TGCTACCTGAGACAGCTCTTTTTGTTTTTTTGAGATGGAGTCTCACCCTGTCACCCAGGGTGGAG TGCTACCTGAGACAGCTCTTTTTGTTTT_____GATGGAGTCTCACCCTGTCACCCAGGGTGGAG TTTTGA T ARHGAP42 Ensembl:ENSG00000165895 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1321556812 Functional Loss DEL dbSNP153 29..33 33 - - - 26086 RMVar_ID_26086 Human_SNP_ID_479140927 A-to-I Human chr11 + 100709059 100709059 100709059 TGCTACCTGAGACAGCTCTTTTTGTTTTTTTGAGATGGAGTCTCACCCTGTCACCCAGGGTGGAG TGCTACCTGAGACAGCTCTTTTTGTTTTTTTGTGATGGAGTCTCACCCTGTCACCCAGGGTGGAG A T ARHGAP42 Ensembl:ENSG00000165895 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs537226984 Functional Loss SNV dbSNP153 33..33 33 - - - 26087 RMVar_ID_26087 Human_SNP_ID_479161693 A-to-I Human chr11 - 100793961 100793961 100793961 TTCCCACCTCAGCCTCCCAAGTACCTAAGACTACAGGCGTGTACCACACCTGGCTAATTTTGTTT TTCCCACCTCAGCCTCCCAAGTACCTAAGACTGCAGGCGTGTACCACACCTGGCTAATTTTGTTT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs942884249 Functional Loss SNV dbSNP153 33..33 33 - - - 26088 RMVar_ID_26088 Human_SNP_ID_479202892 A-to-I Human chr11 + 100960959 100960959 100960959 TAGGACTCTACCGAATAGGAGGAGTGAACTCCAAAGTTCAAAAACTCATGAATACCACATTTTGT TAGGACTCTACCGAATAGGAGGAGTGAACTCCCAAGTTCAAAAACTCATGAATACCACATTTTGT A C ARHGAP42 Ensembl:ENSG00000165895 Protein coding CDS GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1400738460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1290712,Human_Splice_Rec_1290713,Human_Splice_Rec_1290756,Human_Splice_Rec_1290757,Human_Splice_Rec_1290818,Human_Splice_Rec_1290819 RMVar_hsa_circ_34627,RMVar_hsa_circ_352589,RMVar_hsa_circ_11529,RMVar_hsa_circ_19555,RMVar_hsa_circ_315247,RMVar_hsa_circ_124540,RMVar_hsa_circ_11262,RMVar_hsa_circ_152643 26089 RMVar_ID_26089 Human_SNP_ID_479304132 A-to-I Human chr11 - 101357013 101357013 101357013 ATGTATTTTAGTCCATTCTCACATCTCTATAAAGAACTACCTGAGACTGGGTACTTTATAAAGAA ATGTATTTTAGTCCATTCTCACATCTCTATAAGGAACTACCTGAGACTGGGTACTTTATAAAGAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1391593716 Functional Loss SNV dbSNP153 33..33 33 - - - 26090 RMVar_ID_26090 Human_SNP_ID_479304133 A-to-I Human chr11 - 101357015 101357015 101357015 ACATGTATTTTAGTCCATTCTCACATCTCTATAAAGAACTACCTGAGACTGGGTACTTTATAAAG ACATGTATTTTAGTCCATTCTCACATCTCTATGAAGAACTACCTGAGACTGGGTACTTTATAAAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917499693 Functional Loss SNV dbSNP153 33..33 33 - - - 26091 RMVar_ID_26091 Human_SNP_ID_479304134 A-to-I Human chr11 - 101357017 101357017 101357017 TTACATGTATTTTAGTCCATTCTCACATCTCTATAAAGAACTACCTGAGACTGGGTACTTTATAA TTACATGTATTTTAGTCCATTCTCACATCTCTGTAAAGAACTACCTGAGACTGGGTACTTTATAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs141817709 Functional Loss SNV dbSNP153 33..33 33 - - - 26092 RMVar_ID_26092 Human_SNP_ID_479304135 A-to-I Human chr11 - 101357017 101357017 101357017 TTACATGTATTTTAGTCCATTCTCACATCTCTATAAAGAACTACCTGAGACTGGGTACTTTATAA TTACATGTATTTTAGTCCATTCTCACATCTCTCTAAAGAACTACCTGAGACTGGGTACTTTATAA T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs141817709 Functional Loss SNV dbSNP153 33..33 33 - - - 26093 RMVar_ID_26093 Human_SNP_ID_479304139 A-to-I Human chr11 - 101357036 101357036 101357036 TATTACAGCTTTAATCTCATTACATGTATTTTAGTCCATTCTCACATCTCTATAAAGAACTACCT TATTACAGCTTTAATCTCATTACATGTATTTTTGTCCATTCTCACATCTCTATAAAGAACTACCT T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1333988007 Functional Loss SNV dbSNP153 33..33 33 - - - 26094 RMVar_ID_26094 Human_SNP_ID_479306807 A-to-I Human chr11 - 101367069 101367069 101367069 CATAACTACATGGAAACTGAAAAAACTGCTCTAAATGACTACTGGGTAAATAACAAAATGAAGGC CATAACTACATGGAAACTGAAAAAACTGCTCTGAATGACTACTGGGTAAATAACAAAATGAAGGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1440494909 Functional Loss SNV dbSNP153 33..33 33 - - - 26095 RMVar_ID_26095 Human_SNP_ID_479306814 A-to-I Human chr11 - 101367080 101367080 101367080 ACTCAAAACCACATAACTACATGGAAACTGAAAAAACTGCTCTAAATGACTACTGGGTAAATAAC ACTCAAAACCACATAACTACATGGAAACTGAACAAACTGCTCTAAATGACTACTGGGTAAATAAC T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1456369333 Functional Loss SNV dbSNP153 33..33 33 - - - 26096 RMVar_ID_26096 Human_SNP_ID_479430892 A-to-I Human chr11 + 101840920 101840920 101840920 GAAGCATCATGTTGGCTCCCTATCTGATGGCTATTTCTTTGGAATTGGAATGCATAAATGGGACT GAAGCATCATGTTGGCTCCCTATCTGATGGCTGTTTCTTTGGAATTGGAATGCATAAATGGGACT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1426580971 Functional Loss SNV dbSNP153 33..33 33 - - - 26097 RMVar_ID_26097 Human_SNP_ID_479430897 A-to-I Human chr11 + 101840944 101840944 101840944 TGATGGCTATTTCTTTGGAATTGGAATGCATAAATGGGACTGATATACAGAGCAGCTGGAGTAAC TGATGGCTATTTCTTTGGAATTGGAATGCATACATGGGACTGATATACAGAGCAGCTGGAGTAAC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs567386990 Functional Loss SNV dbSNP153 33..33 33 - - - 26098 RMVar_ID_26098 Human_SNP_ID_479431087 A-to-I Human chr11 + 101841595 101841594 101841596 CTCCAACTGCTCTGTATATCAATCCCACTTATACATTCCAATTCCAAAGAAACAGCCATCAGATA CTCCAACTGCTCTGTATATCAATCCCACTTAT__ATTCCAATTCCAAAGAAACAGCCATCAGATA TAC T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1480693758 Functional Loss DEL dbSNP153 33..34 33 - - - 26099 RMVar_ID_26099 Human_SNP_ID_479439938 A-to-I Human chr11 + 101872524 101872524 101872524 TTAGGAATTGGATCCTGAGGGTCTTTTTTAGCAATTGAACCGGACTAACTGCCACTACTAGTGCA TTAGGAATTGGATCCTGAGGGTCTTTTTTAGCGATTGAACCGGACTAACTGCCACTACTAGTGCA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1213547755 Functional Loss SNV dbSNP153 33..33 33 - - - 26100 RMVar_ID_26100 Human_SNP_ID_479469388 A-to-I Human chr11 + 101993984 101993984 101993984 GGCCAGGCATGGTGGCTCATGCCTGTAATCCCAGGACTTTGGGAGGCCGAGGCTGGCTGGTCACC GGCCAGGCATGGTGGCTCATGCCTGTAATCCCTGGACTTTGGGAGGCCGAGGCTGGCTGGTCACC A T CEP126 Ensembl:ENSG00000110318 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs986963945 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_152655,RMVar_hsa_circ_152653,RMVar_hsa_circ_152654,RMVar_hsa_circ_152656,RMVar_hsa_circ_152657 26101 RMVar_ID_26101 Human_SNP_ID_479501803 A-to-I Human chr11 + 102121937 102121937 102121937 CTCCCACCTGAGCCTCCTGAGTAGCTGGGACTACAGGCATCCACCACCATGCCTGGCTAATTTTT CTCCCACCTGAGCCTCCTGAGTAGCTGGGACTGCAGGCATCCACCACCATGCCTGGCTAATTTTT A G YAP1 Ensembl:ENSG00000137693 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1361691159 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72538,RMVar_hsa_circ_326089,RMVar_hsa_circ_337147,RMVar_hsa_circ_282326 26102 RMVar_ID_26102 Human_SNP_ID_479515455 A-to-I Human chr11 + 102174498 102174498 102174498 GGGAGGCTGAGACAGGAGAATCGCTTGAACCCAGGAGGCAGAAGTTGCAGTGAGCTGAGATTGTG GGGAGGCTGAGACAGGAGAATCGCTTGAACCCCGGAGGCAGAAGTTGCAGTGAGCTGAGATTGTG A C YAP1 Ensembl:ENSG00000137693 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1421619675 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72538,RMVar_hsa_circ_337147,RMVar_hsa_circ_282326,RMVar_hsa_circ_274282,RMVar_hsa_circ_367842,RMVar_hsa_circ_335706,RMVar_hsa_circ_45651 26103 RMVar_ID_26103 Human_SNP_ID_479515981 A-to-I Human chr11 + 102176484 102176484 102176484 ATAGAGTAGAATTGGGTCAGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCAATG ATAGAGTAGAATTGGGTCAGGCACGGTGGCTCCCGCCTGTAATCCCAGCACTTTGGGAGGCAATG A C YAP1 Ensembl:ENSG00000137693 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432275456 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5168740,Human_RBP_ID_11503105 RMVar_hsa_circ_72538,RMVar_hsa_circ_337147,RMVar_hsa_circ_282326,RMVar_hsa_circ_274282,RMVar_hsa_circ_367842,RMVar_hsa_circ_335706,RMVar_hsa_circ_45651 26104 RMVar_ID_26104 Human_SNP_ID_479516989 A-to-I Human chr11 + 102180071 102180071 102180071 CGCATCCGTCGTCCAGGCTGGAGTGCAATGGCACAATCTTGGCTCACTGCAACCTCCAACTCCCG CGCATCCGTCGTCCAGGCTGGAGTGCAATGGCGCAATCTTGGCTCACTGCAACCTCCAACTCCCG A G YAP1 Ensembl:ENSG00000137693 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1460271897 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24863407 RMVar_hsa_circ_72538,RMVar_hsa_circ_337147,RMVar_hsa_circ_282326,RMVar_hsa_circ_274282,RMVar_hsa_circ_367842,RMVar_hsa_circ_335706,RMVar_hsa_circ_45651 26105 RMVar_ID_26105 Human_SNP_ID_479517023 A-to-I Human chr11 + 102180183 102180183 102180183 AGGTGTGCGCCACCACACCCGGCTAATTTTGTAGTTTTAGTAGAGATGGGGTTTCACCATGTCAC AGGTGTGCGCCACCACACCCGGCTAATTTTGTGGTTTTAGTAGAGATGGGGTTTCACCATGTCAC A G YAP1 Ensembl:ENSG00000137693 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1267654155 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72538,RMVar_hsa_circ_337147,RMVar_hsa_circ_282326,RMVar_hsa_circ_274282,RMVar_hsa_circ_367842,RMVar_hsa_circ_335706,RMVar_hsa_circ_45651 26106 RMVar_ID_26106 Human_SNP_ID_479517281 A-to-I Human chr11 + 102180878 102180878 102180878 ATGGCCAGTAGTAATTCTCGGTCGGGCATGGTAGCTCGCACCTGTAATCCCACCACTTTGGGAGG ATGGCCAGTAGTAATTCTCGGTCGGGCATGGTGGCTCGCACCTGTAATCCCACCACTTTGGGAGG A G YAP1 Ensembl:ENSG00000137693 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1470243215 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17560723 RMVar_hsa_circ_72538,RMVar_hsa_circ_337147,RMVar_hsa_circ_282326,RMVar_hsa_circ_274282,RMVar_hsa_circ_367842,RMVar_hsa_circ_335706,RMVar_hsa_circ_45651 26107 RMVar_ID_26107 Human_SNP_ID_479517312 A-to-I Human chr11 + 102180965 102180962 102180965 GCTCAGGATTTCGAGACCAGCCTGGGCAACATAATGAGACCCCATCTCTACAGAAAAATTTAAAA GCTCAGGATTTCGAGACCAGCCTGGGCAAC___ATGAGACCCCATCTCTACAGAAAAATTTAAAA CATA C YAP1 Ensembl:ENSG00000137693 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1008231758 Functional Loss DEL dbSNP153 31..33 33 - - - RMVar_hsa_circ_72538,RMVar_hsa_circ_337147,RMVar_hsa_circ_282326,RMVar_hsa_circ_274282,RMVar_hsa_circ_367842,RMVar_hsa_circ_335706,RMVar_hsa_circ_45651 26108 RMVar_ID_26108 Human_SNP_ID_479517341 A-to-I Human chr11 + 102181072 102181072 102181072 CAGGAAGCTGAGGCAGGAGGTCACTTGAGCCCAGGAGTCCAAGGCTGCAGTGAGCCGGGATTGCA CAGGAAGCTGAGGCAGGAGGTCACTTGAGCCCGGGAGTCCAAGGCTGCAGTGAGCCGGGATTGCA A G YAP1 Ensembl:ENSG00000137693 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs905125756 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17560724 RMVar_hsa_circ_72538,RMVar_hsa_circ_337147,RMVar_hsa_circ_282326,RMVar_hsa_circ_274282,RMVar_hsa_circ_367842,RMVar_hsa_circ_335706,RMVar_hsa_circ_45651 26109 RMVar_ID_26109 Human_SNP_ID_479517342 A-to-I Human chr11 + 102181072 102181072 102181072 CAGGAAGCTGAGGCAGGAGGTCACTTGAGCCCAGGAGTCCAAGGCTGCAGTGAGCCGGGATTGCA CAGGAAGCTGAGGCAGGAGGTCACTTGAGCCCTGGAGTCCAAGGCTGCAGTGAGCCGGGATTGCA A T YAP1 Ensembl:ENSG00000137693 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs905125756 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17560724 RMVar_hsa_circ_72538,RMVar_hsa_circ_337147,RMVar_hsa_circ_282326,RMVar_hsa_circ_274282,RMVar_hsa_circ_367842,RMVar_hsa_circ_335706,RMVar_hsa_circ_45651 26110 RMVar_ID_26110 Human_SNP_ID_479517683 A-to-I Human chr11 + 102182027 102182027 102182027 TATTTTTAGTAGAGACGGGGTTTCACCATGTTAGTCAGGCTGGCCTCAAACTCCTGACCTCGTGA TATTTTTAGTAGAGACGGGGTTTCACCATGTTTGTCAGGCTGGCCTCAAACTCCTGACCTCGTGA A T YAP1 Ensembl:ENSG00000137693 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1229432941 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22709891 RMVar_hsa_circ_72538,RMVar_hsa_circ_337147,RMVar_hsa_circ_282326,RMVar_hsa_circ_274282,RMVar_hsa_circ_367842,RMVar_hsa_circ_335706,RMVar_hsa_circ_45651 26111 RMVar_ID_26111 Human_SNP_ID_479517703 A-to-I Human chr11 + 102182071 102182071 102182071 CTCAAACTCCTGACCTCGTGATCCCCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG CTCAAACTCCTGACCTCGTGATCCCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG A G YAP1 Ensembl:ENSG00000137693 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs537701699 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22709891 RMVar_hsa_circ_72538,RMVar_hsa_circ_337147,RMVar_hsa_circ_282326,RMVar_hsa_circ_274282,RMVar_hsa_circ_367842,RMVar_hsa_circ_335706,RMVar_hsa_circ_45651 26112 RMVar_ID_26112 Human_SNP_ID_479520444 A-to-I Human chr11 + 102191711 102191711 102191711 ATTGTTTCTTTCTTTTTTGGAGAGAGGGTCTCACTCTCATCGCCCAGGCTAGAGTGCAGCATGGC ATTGTTTCTTTCTTTTTTGGAGAGAGGGTCTCGCTCTCATCGCCCAGGCTAGAGTGCAGCATGGC A G YAP1 Ensembl:ENSG00000137693 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1565251069 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_337147,RMVar_hsa_circ_282326,RMVar_hsa_circ_274282,RMVar_hsa_circ_367842,RMVar_hsa_circ_335706,RMVar_hsa_circ_152661,RMVar_hsa_circ_278954,RMVar_hsa_circ_300042,RMVar_hsa_circ_339348,RMVar_hsa_circ_296627,RMVar_hsa_circ_43277,RMVar_hsa_circ_152660 26113 RMVar_ID_26113 Human_SNP_ID_479526076 A-to-I Human chr11 + 102213913 102213913 102213913 CTGCCTGGCCAATATGGTGAAAGTCCATCTCTACTAAAAACGGAAAAATTAGCTGGGCTTGGTGG CTGCCTGGCCAATATGGTGAAAGTCCATCTCTCCTAAAAACGGAAAAATTAGCTGGGCTTGGTGG A C YAP1 Ensembl:ENSG00000137693 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1225269896 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 26114 RMVar_ID_26114 Human_SNP_ID_479526083 A-to-I Human chr11 + 102213951 102213951 102213951 AACGGAAAAATTAGCTGGGCTTGGTGGCATGCACCTGTAGTCCCAGCTACTCAGGAGGCTGAGGT AACGGAAAAATTAGCTGGGCTTGGTGGCATGCCCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGT A C YAP1 Ensembl:ENSG00000137693 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1409259020 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 26115 RMVar_ID_26115 Human_SNP_ID_479526431 A-to-I Human chr11 + 102215530 102215530 102215530 TGGAGTTTCACTCATCACCCAGGCTGGAGTGCAATGGCACGATCTCGGCTCACTGCAACCTCCTC TGGAGTTTCACTCATCACCCAGGCTGGAGTGCGATGGCACGATCTCGGCTCACTGCAACCTCCTC A G YAP1 Ensembl:ENSG00000137693 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1412210572 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 26116 RMVar_ID_26116 Human_SNP_ID_479531823 A-to-I Human chr11 + 102236322 102236322 102236322 TGGGGTTTCACCATGTTGTCCAGGCTGGTCTCAAACTCCTGAGCTCAAGTAATCAATCTGCCCAC TGGGGTTTCACCATGTTGTCCAGGCTGGTCTCGAACTCCTGAGCTCAAGTAATCAATCTGCCCAC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1452918001 Functional Loss SNV dbSNP153 33..33 33 - - - 26117 RMVar_ID_26117 Human_SNP_ID_479554312 A-to-I Human chr11 + 102326870 102326870 102326870 AGCTGGGATTACAGGTGCACGCTAGCATGCCCAGCTAATTTTTGTATTTTTGTAGAGACAGGGTT AGCTGGGATTACAGGTGCACGCTAGCATGCCCGGCTAATTTTTGTATTTTTGTAGAGACAGGGTT A G BIRC3 Ensembl:ENSG00000023445 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1176368855 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_152669,RMVar_hsa_circ_122058 26118 RMVar_ID_26118 Human_SNP_ID_479555565 A-to-I Human chr11 + 102331676 102331676 102331676 GACAATTATTAATTTTTTTTTGAGACAGTCTTACTCTGTCACCCATGCTGGAGTGCAGTGGCATG GACAATTATTAATTTTTTTTTGAGACAGTCTTCCTCTGTCACCCATGCTGGAGTGCAGTGGCATG A C BIRC3 Ensembl:ENSG00000023445 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1057162718 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75948,RMVar_hsa_circ_68032,RMVar_hsa_circ_152670 26119 RMVar_ID_26119 Human_SNP_ID_479555607 A-to-I Human chr11 + 102331861 102331861 102331861 AGGGATTTCTCCATGTTGGCCACACTGGTCTCAAACTCCTGACCTCAAGTGATCCGCCCGCCTCG AGGGATTTCTCCATGTTGGCCACACTGGTCTCTAACTCCTGACCTCAAGTGATCCGCCCGCCTCG A T BIRC3 Ensembl:ENSG00000023445 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs529903663 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75948,RMVar_hsa_circ_68032,RMVar_hsa_circ_152670 26120 RMVar_ID_26120 Human_SNP_ID_479556022 A-to-I Human chr11 + 102333666 102333666 102333666 TACTCAGGAGGCTCAGGTACAAAAATAGCTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCTGAGA TACTCAGGAGGCTCAGGTACAAAAATAGCTTGGACCTGGGAGGCAGAGGTTGCAGTGAGCTGAGA A G BIRC3 Ensembl:ENSG00000023445 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1399964319 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75948,RMVar_hsa_circ_68032,RMVar_hsa_circ_152670 26121 RMVar_ID_26121 Human_SNP_ID_479556135 A-to-I Human chr11 + 102334155 102334155 102334155 AATTACAAAAATAAATCTTAGATTGAAAAACTAGTATACTTCAACACCAAGTTTGTATTTTTATT AATTACAAAAATAAATCTTAGATTGAAAAACTGGTATACTTCAACACCAAGTTTGTATTTTTATT A G BIRC3 Ensembl:ENSG00000023445 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1421953102 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75948,RMVar_hsa_circ_68032,RMVar_hsa_circ_152670 26122 RMVar_ID_26122 Human_SNP_ID_479556140 A-to-I Human chr11 + 102334185 102334185 102334185 CTAGTATACTTCAACACCAAGTTTGTATTTTTATTTTCTAATATATCCCTACTTTGCTAATAGAA CTAGTATACTTCAACACCAAGTTTGTATTTTTGTTTTCTAATATATCCCTACTTTGCTAATAGAA A G BIRC3 Ensembl:ENSG00000023445 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs964297358 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75948,RMVar_hsa_circ_68032,RMVar_hsa_circ_152670 26123 RMVar_ID_26123 Human_SNP_ID_479748333 A-to-I Human chr11 - 103064345 103064345 103064345 CAATCAAAGTATCGTGTTATGAACAAAGATCAATGGTACAATGTATTAGAATTCAGCAGAACAGT CAATCAAAGTATCGTGTTATGAACAAAGATCAGTGGTACAATGTATTAGAATTCAGCAGAACAGT T C DCUN1D5 Ensembl:ENSG00000137692 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs370307520 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1453538,Human_RBP_ID_1774628,Human_RBP_ID_11505513,Human_RBP_ID_18246840,Human_RBP_ID_18602047,Human_RBP_ID_27613855 Human_Splice_Rec_1291994,Human_Splice_Rec_1291995,Human_Splice_Rec_1292018,Human_Splice_Rec_1292019,Human_Splice_Rec_1292026,Human_Splice_Rec_1292027,Human_Splice_Rec_1292040,Human_Splice_Rec_1292041,Human_Splice_Rec_1292052,Human_Splice_Rec_1292053,Human_Splice_Rec_1292062,Human_Splice_Rec_1292063,Human_Splice_Rec_1292074 Human_miRNA_ID_1129615,Human_miRNA_ID_1772843 RMVar_hsa_circ_9395,RMVar_hsa_circ_152688,RMVar_hsa_circ_22207 26124 RMVar_ID_26124 Human_SNP_ID_479750608 A-to-I Human chr11 - 103073890 103073890 103073890 TTTCTATTTTTTAGTAGTGACAGGATTTCACCATGTTGGCCAGGCTGGTCTCAAAATCCTGACCT TTTCTATTTTTTAGTAGTGACAGGATTTCACCGTGTTGGCCAGGCTGGTCTCAAAATCCTGACCT T C DCUN1D5 Ensembl:ENSG00000137692 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1036226071 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22207,RMVar_hsa_circ_110914,RMVar_hsa_circ_288675,RMVar_hsa_circ_114493,RMVar_hsa_circ_152690,RMVar_hsa_circ_152691,RMVar_hsa_circ_152689 26125 RMVar_ID_26125 Human_SNP_ID_480380771 A-to-I Human chr11 + 105628633 105628633 105628633 TTGTAAGTTTCCTGTGTCTCCCCAGCCATGTGAAACTGTAGTCAATTAAACCTCTTTCCTTTGTA TTGTAAGTTTCCTGTGTCTCCCCAGCCATGTGCAACTGTAGTCAATTAAACCTCTTTCCTTTGTA A C GRIA4 Ensembl:ENSG00000152578 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1378499422 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47670 26126 RMVar_ID_26126 Human_SNP_ID_480384578 A-to-I Human chr11 + 105643798 105643797 105643798 TGGAGTGCAGTGACATCATCTCTGCTCAGTGCAACCTCTGCCTCCCAGGTTGAAGCGATTCTCCT TGGAGTGCAGTGACATCATCTCTGCTCAGTGC_ACCTCTGCCTCCCAGGTTGAAGCGATTCTCCT CA C GRIA4 Ensembl:ENSG00000152578 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs757637120 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_47670 26127 RMVar_ID_26127 Human_SNP_ID_480385580 A-to-I Human chr11 + 105647726 105647726 105647726 CAGAAAACCAAATACTGCACACTCTCACTTATAAGCGGGAGCTCAATGATGAGAGCACATGGACA CAGAAAACCAAATACTGCACACTCTCACTTATGAGCGGGAGCTCAATGATGAGAGCACATGGACA A G GRIA4 Ensembl:ENSG00000152578 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1050002089 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47670 26128 RMVar_ID_26128 Human_SNP_ID_480397815 A-to-I Human chr11 + 105697343 105697343 105697343 AAAGCCTAAATGCATGTACAAGTGTATATGCCAAATTTGCCTACAACTTTAGGACTCTCAGGATT AAAGCCTAAATGCATGTACAAGTGTATATGCCCAATTTGCCTACAACTTTAGGACTCTCAGGATT A C GRIA4 Ensembl:ENSG00000152578 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs989026879 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47670 26129 RMVar_ID_26129 Human_SNP_ID_480480732 A-to-I Human chr11 - 106058690 106058690 106058690 GCTGGGCACGGTGGCTCACGCCTGTAATCCCAACACCCTAAGAGGCCAAGGCGGGCGGATCACCT GCTGGGCACGGTGGCTCACGCCTGTAATCCCAGCACCCTAAGAGGCCAAGGCGGGCGGATCACCT T C KBTBD3 Ensembl:ENSG00000182359 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913487197 Functional Loss SNV dbSNP153 33..33 33 - - - 26130 RMVar_ID_26130 Human_SNP_ID_480481512 A-to-I Human chr11 - 106061737 106061737 106061737 AGAAAAACTATAAGGAATTAGCTCATGTGATTATGGAGGCTGAGAAGACCCAAGATTTGTAGTCA AGAAAAACTATAAGGAATTAGCTCATGTGATTGTGGAGGCTGAGAAGACCCAAGATTTGTAGTCA T C KBTBD3 Ensembl:ENSG00000182359 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1205655096 Functional Loss SNV dbSNP153 33..33 33 - - - 26131 RMVar_ID_26131 Human_SNP_ID_480782447 A-to-I Human chr11 - 107291446 107291446 107291446 GTATTGGTATAAAAAAAGAGACAAATAGACTAATGAAACAGAATAGAGAACCGGGGAATAAATCC GTATTGGTATAAAAAAAGAGACAAATAGACTATTGAAACAGAATAGAGAACCGGGGAATAAATCC T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs943124501 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2247699,Human_RBP_ID_11510048 26132 RMVar_ID_26132 Human_SNP_ID_480782448 A-to-I Human chr11 - 107291446 107291446 107291446 GTATTGGTATAAAAAAAGAGACAAATAGACTAATGAAACAGAATAGAGAACCGGGGAATAAATCC GTATTGGTATAAAAAAAGAGACAAATAGACTAGTGAAACAGAATAGAGAACCGGGGAATAAATCC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs943124501 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2247699,Human_RBP_ID_11510048 26133 RMVar_ID_26133 Human_SNP_ID_480785104 A-to-I Human chr11 - 107300938 107300938 107300938 TGCTCACTGCAGCGTCAACCTTCTGGGCTCAAACGATCCTCCGTTCTTAGCCTCCCAAGTAGCTG TGCTCACTGCAGCGTCAACCTTCTGGGCTCAATCGATCCTCCGTTCTTAGCCTCCCAAGTAGCTG T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs759850182 Functional Loss SNV dbSNP153 33..33 33 - - - 26134 RMVar_ID_26134 Human_SNP_ID_480785105 A-to-I Human chr11 - 107300938 107300938 107300938 TGCTCACTGCAGCGTCAACCTTCTGGGCTCAAACGATCCTCCGTTCTTAGCCTCCCAAGTAGCTG TGCTCACTGCAGCGTCAACCTTCTGGGCTCAAGCGATCCTCCGTTCTTAGCCTCCCAAGTAGCTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs759850182 Functional Loss SNV dbSNP153 33..33 33 - - - 26135 RMVar_ID_26135 Human_SNP_ID_480786637 A-to-I Human chr11 - 107307204 107307204 107307204 CCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGTGCACACCACCATACCCAGCTAATTTTTTA CCTGCCTCAGCCTCCTGAGTAGCTGGGACTACGGGTGCACACCACCATACCCAGCTAATTTTTTA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1446498760 Functional Loss SNV dbSNP153 33..33 33 - - - 26136 RMVar_ID_26136 Human_SNP_ID_480913712 A-to-I Human chr11 - 107831500 107831500 107831500 GTCTTGTTGGTTGGGTGTGGTGGTGCACGTCTATAATCCCAGTGCTTTGGGAGGTCTAGGCATGA GTCTTGTTGGTTGGGTGTGGTGGTGCACGTCTGTAATCCCAGTGCTTTGGGAGGTCTAGGCATGA T C SLC35F2 Ensembl:ENSG00000110660 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978091866 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1886,RMVar_hsa_circ_152809,RMVar_hsa_circ_333002,RMVar_hsa_circ_152818 26137 RMVar_ID_26137 Human_SNP_ID_480964336 A-to-I Human chr11 + 108027683 108027683 108027683 CGCCCGCCTCAGCCTCCCAGTGTTGGGATTACAAGCATGAACTATTGCGCCTGGCTCCTCGTTTC CGCCCGCCTCAGCCTCCCAGTGTTGGGATTACCAGCATGAACTATTGCGCCTGGCTCCTCGTTTC A C CUL5 Ensembl:ENSG00000166266 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991407324 Functional Loss SNV dbSNP153 33..33 33 - - - 26138 RMVar_ID_26138 Human_SNP_ID_480964337 A-to-I Human chr11 + 108027683 108027683 108027683 CGCCCGCCTCAGCCTCCCAGTGTTGGGATTACAAGCATGAACTATTGCGCCTGGCTCCTCGTTTC CGCCCGCCTCAGCCTCCCAGTGTTGGGATTACGAGCATGAACTATTGCGCCTGGCTCCTCGTTTC A G CUL5 Ensembl:ENSG00000166266 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991407324 Functional Loss SNV dbSNP153 33..33 33 - - - 26139 RMVar_ID_26139 Human_SNP_ID_480971849 A-to-I Human chr11 + 108057302 108057302 108057302 CTCCCACCTCGACCTCCCAGAGTGCTAGGATTACAGGCACGAGCCACGGCACTTGGCAGTAACGG CTCCCACCTCGACCTCCCAGAGTGCTAGGATTCCAGGCACGAGCCACGGCACTTGGCAGTAACGG A C CUL5 Ensembl:ENSG00000166266 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs995168947 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33769,RMVar_hsa_circ_298184,RMVar_hsa_circ_326927,RMVar_hsa_circ_317351,RMVar_hsa_circ_18486,RMVar_hsa_circ_334417,RMVar_hsa_circ_349084,RMVar_hsa_circ_373159,RMVar_hsa_circ_316121,RMVar_hsa_circ_278592,RMVar_hsa_circ_21799,RMVar_hsa_circ_152823,RMVar_hsa_circ_152825,RMVar_hsa_circ_152826,RMVar_hsa_circ_152827,RMVar_hsa_circ_152824,RMVar_hsa_circ_152830,RMVar_hsa_circ_35432,RMVar_hsa_circ_274033,RMVar_hsa_circ_317849,RMVar_hsa_circ_335485,RMVar_hsa_circ_271262,RMVar_hsa_circ_152832,RMVar_hsa_circ_152833,RMVar_hsa_circ_152831,RMVar_hsa_circ_152828,RMVar_hsa_circ_152829,RMVar_hsa_circ_325339,RMVar_hsa_circ_333692,RMVar_hsa_circ_334745,RMVar_hsa_circ_312086,RMVar_hsa_circ_291185,RMVar_hsa_circ_309912,RMVar_hsa_circ_93465,RMVar_hsa_circ_33750,RMVar_hsa_circ_152836,RMVar_hsa_circ_152838,RMVar_hsa_circ_152840,RMVar_hsa_circ_44439,RMVar_hsa_circ_152841,RMVar_hsa_circ_152839,RMVar_hsa_circ_152837,RMVar_hsa_circ_36598,RMVar_hsa_circ_40990,RMVar_hsa_circ_60796 26140 RMVar_ID_26140 Human_SNP_ID_480972194 A-to-I Human chr11 + 108058509 108058509 108058509 TGACTTCGTGATCTGCCCGCGGCGGCCTCCCAAAGTGCTGGGATTACAGACGTGAGCCACTGCAC TGACTTCGTGATCTGCCCGCGGCGGCCTCCCAGAGTGCTGGGATTACAGACGTGAGCCACTGCAC A G CUL5 Ensembl:ENSG00000166266 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs553102070 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33769,RMVar_hsa_circ_298184,RMVar_hsa_circ_326927,RMVar_hsa_circ_317351,RMVar_hsa_circ_18486,RMVar_hsa_circ_334417,RMVar_hsa_circ_349084,RMVar_hsa_circ_373159,RMVar_hsa_circ_316121,RMVar_hsa_circ_278592,RMVar_hsa_circ_21799,RMVar_hsa_circ_152823,RMVar_hsa_circ_152825,RMVar_hsa_circ_152826,RMVar_hsa_circ_152827,RMVar_hsa_circ_152824,RMVar_hsa_circ_152830,RMVar_hsa_circ_35432,RMVar_hsa_circ_274033,RMVar_hsa_circ_317849,RMVar_hsa_circ_335485,RMVar_hsa_circ_271262,RMVar_hsa_circ_152832,RMVar_hsa_circ_152833,RMVar_hsa_circ_152831,RMVar_hsa_circ_152828,RMVar_hsa_circ_152829,RMVar_hsa_circ_325339,RMVar_hsa_circ_333692,RMVar_hsa_circ_334745,RMVar_hsa_circ_312086,RMVar_hsa_circ_291185,RMVar_hsa_circ_309912,RMVar_hsa_circ_93465,RMVar_hsa_circ_33750,RMVar_hsa_circ_152836,RMVar_hsa_circ_152838,RMVar_hsa_circ_152840,RMVar_hsa_circ_44439,RMVar_hsa_circ_152841,RMVar_hsa_circ_152839,RMVar_hsa_circ_152837,RMVar_hsa_circ_36598,RMVar_hsa_circ_40990,RMVar_hsa_circ_60796 26141 RMVar_ID_26141 Human_SNP_ID_480975772 A-to-I Human chr11 + 108071949 108071949 108071949 CTATGATCCCAGCACTTTGAGAGACCAAGGCGAGAGGATTGTGTGAGCCCCGAAGTTTGAGACCA CTATGATCCCAGCACTTTGAGAGACCAAGGCGGGAGGATTGTGTGAGCCCCGAAGTTTGAGACCA A G CUL5 Ensembl:ENSG00000166266 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1268708897 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11512886 RMVar_hsa_circ_33769,RMVar_hsa_circ_298184,RMVar_hsa_circ_326927,RMVar_hsa_circ_317351,RMVar_hsa_circ_18486,RMVar_hsa_circ_334417,RMVar_hsa_circ_349084,RMVar_hsa_circ_316121,RMVar_hsa_circ_278592,RMVar_hsa_circ_21799,RMVar_hsa_circ_152825,RMVar_hsa_circ_152826,RMVar_hsa_circ_152827,RMVar_hsa_circ_152830,RMVar_hsa_circ_35432,RMVar_hsa_circ_274033,RMVar_hsa_circ_317849,RMVar_hsa_circ_335485,RMVar_hsa_circ_271262,RMVar_hsa_circ_152831,RMVar_hsa_circ_152828,RMVar_hsa_circ_152829,RMVar_hsa_circ_325339,RMVar_hsa_circ_333692,RMVar_hsa_circ_334745,RMVar_hsa_circ_312086,RMVar_hsa_circ_291185,RMVar_hsa_circ_309912,RMVar_hsa_circ_93465,RMVar_hsa_circ_33750,RMVar_hsa_circ_152836,RMVar_hsa_circ_152838,RMVar_hsa_circ_152840,RMVar_hsa_circ_44439,RMVar_hsa_circ_152841,RMVar_hsa_circ_152839,RMVar_hsa_circ_152837,RMVar_hsa_circ_36598,RMVar_hsa_circ_423,RMVar_hsa_circ_152843,RMVar_hsa_circ_40990,RMVar_hsa_circ_60796,RMVar_hsa_circ_152844,RMVar_hsa_circ_279941,RMVar_hsa_circ_298685,RMVar_hsa_circ_338567,RMVar_hsa_circ_291013,RMVar_hsa_circ_97512,RMVar_hsa_circ_152846,RMVar_hsa_circ_152848,RMVar_hsa_circ_152849,RMVar_hsa_circ_152847,RMVar_hsa_circ_152845 26142 RMVar_ID_26142 Human_SNP_ID_480977709 A-to-I Human chr11 + 108079127 108079127 108079127 TATTAATTTTAATTTATTTATTTATTCGAGACAGGGTCTCACTCTGTCACCCAGGCTGGAGTGCA TATTAATTTTAATTTATTTATTTATTCGAGACGGGGTCTCACTCTGTCACCCAGGCTGGAGTGCA A G CUL5 Ensembl:ENSG00000166266 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1443661648 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16880,RMVar_hsa_circ_33769,RMVar_hsa_circ_298184,RMVar_hsa_circ_18486,RMVar_hsa_circ_334417,RMVar_hsa_circ_349084,RMVar_hsa_circ_152827,RMVar_hsa_circ_35432,RMVar_hsa_circ_317849,RMVar_hsa_circ_152828,RMVar_hsa_circ_152829,RMVar_hsa_circ_333692,RMVar_hsa_circ_312086,RMVar_hsa_circ_291185,RMVar_hsa_circ_93465,RMVar_hsa_circ_152840,RMVar_hsa_circ_44439,RMVar_hsa_circ_152841,RMVar_hsa_circ_152839,RMVar_hsa_circ_36598,RMVar_hsa_circ_40990,RMVar_hsa_circ_60796,RMVar_hsa_circ_338567,RMVar_hsa_circ_291013,RMVar_hsa_circ_97512,RMVar_hsa_circ_152848,RMVar_hsa_circ_152849,RMVar_hsa_circ_152847,RMVar_hsa_circ_341472,RMVar_hsa_circ_57643,RMVar_hsa_circ_316851,RMVar_hsa_circ_152850,RMVar_hsa_circ_152851,RMVar_hsa_circ_351238,RMVar_hsa_circ_265154 26143 RMVar_ID_26143 Human_SNP_ID_480977712 A-to-I Human chr11 + 108079135 108079135 108079135 TTAATTTATTTATTTATTCGAGACAGGGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGTACG TTAATTTATTTATTTATTCGAGACAGGGTCTCCCTCTGTCACCCAGGCTGGAGTGCAGTGGTACG A C CUL5 Ensembl:ENSG00000166266 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1469965918 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16880,RMVar_hsa_circ_33769,RMVar_hsa_circ_298184,RMVar_hsa_circ_18486,RMVar_hsa_circ_334417,RMVar_hsa_circ_349084,RMVar_hsa_circ_152827,RMVar_hsa_circ_35432,RMVar_hsa_circ_317849,RMVar_hsa_circ_152828,RMVar_hsa_circ_152829,RMVar_hsa_circ_333692,RMVar_hsa_circ_312086,RMVar_hsa_circ_291185,RMVar_hsa_circ_93465,RMVar_hsa_circ_152840,RMVar_hsa_circ_44439,RMVar_hsa_circ_152841,RMVar_hsa_circ_152839,RMVar_hsa_circ_36598,RMVar_hsa_circ_40990,RMVar_hsa_circ_60796,RMVar_hsa_circ_338567,RMVar_hsa_circ_291013,RMVar_hsa_circ_97512,RMVar_hsa_circ_152848,RMVar_hsa_circ_152849,RMVar_hsa_circ_152847,RMVar_hsa_circ_341472,RMVar_hsa_circ_57643,RMVar_hsa_circ_316851,RMVar_hsa_circ_152850,RMVar_hsa_circ_152851,RMVar_hsa_circ_351238,RMVar_hsa_circ_265154 26144 RMVar_ID_26144 Human_SNP_ID_480978291 A-to-I Human chr11 + 108081168 108081168 108081168 AAATTAGCCAGGCGTGGTGGCTCATGCCTGTGATCCCAGCTACTTGGGAGGCTGAGACAGGAGAA AAATTAGCCAGGCGTGGTGGCTCATGCCTGTGGTCCCAGCTACTTGGGAGGCTGAGACAGGAGAA A G CUL5 Ensembl:ENSG00000166266 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1288479513 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16880,RMVar_hsa_circ_33769,RMVar_hsa_circ_298184,RMVar_hsa_circ_18486,RMVar_hsa_circ_334417,RMVar_hsa_circ_349084,RMVar_hsa_circ_152827,RMVar_hsa_circ_35432,RMVar_hsa_circ_317849,RMVar_hsa_circ_152828,RMVar_hsa_circ_152829,RMVar_hsa_circ_333692,RMVar_hsa_circ_312086,RMVar_hsa_circ_291185,RMVar_hsa_circ_93465,RMVar_hsa_circ_152840,RMVar_hsa_circ_44439,RMVar_hsa_circ_152841,RMVar_hsa_circ_152839,RMVar_hsa_circ_36598,RMVar_hsa_circ_40990,RMVar_hsa_circ_60796,RMVar_hsa_circ_338567,RMVar_hsa_circ_291013,RMVar_hsa_circ_97512,RMVar_hsa_circ_152848,RMVar_hsa_circ_152849,RMVar_hsa_circ_152847,RMVar_hsa_circ_341472,RMVar_hsa_circ_57643,RMVar_hsa_circ_316851,RMVar_hsa_circ_152850,RMVar_hsa_circ_152851,RMVar_hsa_circ_351238,RMVar_hsa_circ_265154 26145 RMVar_ID_26145 Human_SNP_ID_480978636 A-to-I Human chr11 + 108082420 108082420 108082420 CTCCCACCTCAGCCACCTGAGTAGCTAGGACCACAGGTTCAGGCCACCACACCTGGCTATATTAT CTCCCACCTCAGCCACCTGAGTAGCTAGGACCGCAGGTTCAGGCCACCACACCTGGCTATATTAT A G CUL5 Ensembl:ENSG00000166266 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1290698204 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16880,RMVar_hsa_circ_33769,RMVar_hsa_circ_298184,RMVar_hsa_circ_18486,RMVar_hsa_circ_334417,RMVar_hsa_circ_349084,RMVar_hsa_circ_152827,RMVar_hsa_circ_35432,RMVar_hsa_circ_317849,RMVar_hsa_circ_152828,RMVar_hsa_circ_152829,RMVar_hsa_circ_333692,RMVar_hsa_circ_312086,RMVar_hsa_circ_291185,RMVar_hsa_circ_93465,RMVar_hsa_circ_152840,RMVar_hsa_circ_44439,RMVar_hsa_circ_152841,RMVar_hsa_circ_152839,RMVar_hsa_circ_36598,RMVar_hsa_circ_40990,RMVar_hsa_circ_60796,RMVar_hsa_circ_338567,RMVar_hsa_circ_291013,RMVar_hsa_circ_97512,RMVar_hsa_circ_152848,RMVar_hsa_circ_152849,RMVar_hsa_circ_152847,RMVar_hsa_circ_341472,RMVar_hsa_circ_57643,RMVar_hsa_circ_316851,RMVar_hsa_circ_152850,RMVar_hsa_circ_152851,RMVar_hsa_circ_351238,RMVar_hsa_circ_265154 26146 RMVar_ID_26146 Human_SNP_ID_480980981 A-to-I Human chr11 + 108091435 108091435 108091435 AAACAAGGCTAGGCATGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGAGGGCAG AAACAAGGCTAGGCATGGTGGCTCACACCTGTGATCCCAGCACTTTGGGAGGCTGAGGAGGGCAG A G CUL5 Ensembl:ENSG00000166266 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs891744190 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33769,RMVar_hsa_circ_18486,RMVar_hsa_circ_334417,RMVar_hsa_circ_152827,RMVar_hsa_circ_35432,RMVar_hsa_circ_152828,RMVar_hsa_circ_312086,RMVar_hsa_circ_291185,RMVar_hsa_circ_93465,RMVar_hsa_circ_152840,RMVar_hsa_circ_44439,RMVar_hsa_circ_152841,RMVar_hsa_circ_36598,RMVar_hsa_circ_40990,RMVar_hsa_circ_60796,RMVar_hsa_circ_338567,RMVar_hsa_circ_97512,RMVar_hsa_circ_152848,RMVar_hsa_circ_152849,RMVar_hsa_circ_341472,RMVar_hsa_circ_108111,RMVar_hsa_circ_152851,RMVar_hsa_circ_265154,RMVar_hsa_circ_275286,RMVar_hsa_circ_301864,RMVar_hsa_circ_152853,RMVar_hsa_circ_152854,RMVar_hsa_circ_152855 26147 RMVar_ID_26147 Human_SNP_ID_480982154 A-to-I Human chr11 + 108096059 108096059 108096059 TAGAGGTTGCAGTGAGCCAAGATTGCGCCACTACACTCCAGCCCAGGCAACAGAGTGAGAACTCC TAGAGGTTGCAGTGAGCCAAGATTGCGCCACTGCACTCCAGCCCAGGCAACAGAGTGAGAACTCC A G CUL5 Ensembl:ENSG00000166266 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs558615893 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33769,RMVar_hsa_circ_334417,RMVar_hsa_circ_152827,RMVar_hsa_circ_35432,RMVar_hsa_circ_152828,RMVar_hsa_circ_312086,RMVar_hsa_circ_93465,RMVar_hsa_circ_152840,RMVar_hsa_circ_152841,RMVar_hsa_circ_40990,RMVar_hsa_circ_338567,RMVar_hsa_circ_152849,RMVar_hsa_circ_31863,RMVar_hsa_circ_108111,RMVar_hsa_circ_152851,RMVar_hsa_circ_265154,RMVar_hsa_circ_275286,RMVar_hsa_circ_152854,RMVar_hsa_circ_152856,RMVar_hsa_circ_306126,RMVar_hsa_circ_152855,RMVar_hsa_circ_152857,RMVar_hsa_circ_64267 26148 RMVar_ID_26148 Human_SNP_ID_480982363 A-to-I Human chr11 + 108096630 108096630 108096630 CTCTTGTCGCTCAGGCTGGAGTGCAATGGCGCAATCTCAGCTCACTGCAACCTCCGCCTCCAGGG CTCTTGTCGCTCAGGCTGGAGTGCAATGGCGCCATCTCAGCTCACTGCAACCTCCGCCTCCAGGG A C CUL5 Ensembl:ENSG00000166266 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1301237270 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33769,RMVar_hsa_circ_334417,RMVar_hsa_circ_152827,RMVar_hsa_circ_35432,RMVar_hsa_circ_152828,RMVar_hsa_circ_312086,RMVar_hsa_circ_93465,RMVar_hsa_circ_152840,RMVar_hsa_circ_152841,RMVar_hsa_circ_40990,RMVar_hsa_circ_338567,RMVar_hsa_circ_152849,RMVar_hsa_circ_31863,RMVar_hsa_circ_108111,RMVar_hsa_circ_152851,RMVar_hsa_circ_265154,RMVar_hsa_circ_275286,RMVar_hsa_circ_152854,RMVar_hsa_circ_152856,RMVar_hsa_circ_306126,RMVar_hsa_circ_152855,RMVar_hsa_circ_152857,RMVar_hsa_circ_64267 26149 RMVar_ID_26149 Human_SNP_ID_480982378 A-to-I Human chr11 + 108096671 108096671 108096671 TCACTGCAACCTCCGCCTCCAGGGTTTAAGCGATTCTCCTACCTCAGCCTCCCAAGTAGCTGGAA TCACTGCAACCTCCGCCTCCAGGGTTTAAGCGTTTCTCCTACCTCAGCCTCCCAAGTAGCTGGAA A T CUL5 Ensembl:ENSG00000166266 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs574989514 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33769,RMVar_hsa_circ_334417,RMVar_hsa_circ_152827,RMVar_hsa_circ_35432,RMVar_hsa_circ_152828,RMVar_hsa_circ_312086,RMVar_hsa_circ_93465,RMVar_hsa_circ_152840,RMVar_hsa_circ_152841,RMVar_hsa_circ_40990,RMVar_hsa_circ_338567,RMVar_hsa_circ_152849,RMVar_hsa_circ_31863,RMVar_hsa_circ_108111,RMVar_hsa_circ_152851,RMVar_hsa_circ_265154,RMVar_hsa_circ_275286,RMVar_hsa_circ_152854,RMVar_hsa_circ_152856,RMVar_hsa_circ_306126,RMVar_hsa_circ_152855,RMVar_hsa_circ_152857,RMVar_hsa_circ_64267 26150 RMVar_ID_26150 Human_SNP_ID_480982380 A-to-I Human chr11 + 108096679 108096679 108096679 ACCTCCGCCTCCAGGGTTTAAGCGATTCTCCTACCTCAGCCTCCCAAGTAGCTGGAATTACAGGC ACCTCCGCCTCCAGGGTTTAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGAATTACAGGC A G CUL5 Ensembl:ENSG00000166266 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs535821291 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24865574 RMVar_hsa_circ_33769,RMVar_hsa_circ_334417,RMVar_hsa_circ_152827,RMVar_hsa_circ_35432,RMVar_hsa_circ_152828,RMVar_hsa_circ_312086,RMVar_hsa_circ_93465,RMVar_hsa_circ_152840,RMVar_hsa_circ_152841,RMVar_hsa_circ_40990,RMVar_hsa_circ_338567,RMVar_hsa_circ_152849,RMVar_hsa_circ_31863,RMVar_hsa_circ_108111,RMVar_hsa_circ_152851,RMVar_hsa_circ_265154,RMVar_hsa_circ_275286,RMVar_hsa_circ_152854,RMVar_hsa_circ_152856,RMVar_hsa_circ_306126,RMVar_hsa_circ_152855,RMVar_hsa_circ_152857,RMVar_hsa_circ_64267 26151 RMVar_ID_26151 Human_SNP_ID_480982406 A-to-I Human chr11 + 108096766 108096766 108096766 TTTTATATTTTTAGTGGAGACGGGGTTTCACCATGTTGGTCAGGCTAGTCTCAAACTCCTGACCT TTTTATATTTTTAGTGGAGACGGGGTTTCACCGTGTTGGTCAGGCTAGTCTCAAACTCCTGACCT A G CUL5 Ensembl:ENSG00000166266 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs557094112 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33769,RMVar_hsa_circ_334417,RMVar_hsa_circ_152827,RMVar_hsa_circ_35432,RMVar_hsa_circ_152828,RMVar_hsa_circ_312086,RMVar_hsa_circ_93465,RMVar_hsa_circ_152840,RMVar_hsa_circ_152841,RMVar_hsa_circ_40990,RMVar_hsa_circ_338567,RMVar_hsa_circ_152849,RMVar_hsa_circ_31863,RMVar_hsa_circ_108111,RMVar_hsa_circ_152851,RMVar_hsa_circ_265154,RMVar_hsa_circ_275286,RMVar_hsa_circ_152854,RMVar_hsa_circ_152856,RMVar_hsa_circ_306126,RMVar_hsa_circ_152855,RMVar_hsa_circ_152857,RMVar_hsa_circ_64267 26152 RMVar_ID_26152 Human_SNP_ID_480982408 A-to-I Human chr11 + 108096780 108096780 108096780 TGGAGACGGGGTTTCACCATGTTGGTCAGGCTAGTCTCAAACTCCTGACCTCAGGTAATTTGCCC TGGAGACGGGGTTTCACCATGTTGGTCAGGCTGGTCTCAAACTCCTGACCTCAGGTAATTTGCCC A G CUL5 Ensembl:ENSG00000166266 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1260965780 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33769,RMVar_hsa_circ_334417,RMVar_hsa_circ_152827,RMVar_hsa_circ_35432,RMVar_hsa_circ_152828,RMVar_hsa_circ_312086,RMVar_hsa_circ_93465,RMVar_hsa_circ_152840,RMVar_hsa_circ_152841,RMVar_hsa_circ_40990,RMVar_hsa_circ_338567,RMVar_hsa_circ_152849,RMVar_hsa_circ_31863,RMVar_hsa_circ_108111,RMVar_hsa_circ_152851,RMVar_hsa_circ_265154,RMVar_hsa_circ_275286,RMVar_hsa_circ_152854,RMVar_hsa_circ_152856,RMVar_hsa_circ_306126,RMVar_hsa_circ_152855,RMVar_hsa_circ_152857,RMVar_hsa_circ_64267 26153 RMVar_ID_26153 Human_SNP_ID_480982413 A-to-I Human chr11 + 108096786 108096786 108096786 CGGGGTTTCACCATGTTGGTCAGGCTAGTCTCAAACTCCTGACCTCAGGTAATTTGCCCGCCTCG CGGGGTTTCACCATGTTGGTCAGGCTAGTCTCGAACTCCTGACCTCAGGTAATTTGCCCGCCTCG A G CUL5 Ensembl:ENSG00000166266 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1199136601 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33769,RMVar_hsa_circ_334417,RMVar_hsa_circ_152827,RMVar_hsa_circ_35432,RMVar_hsa_circ_152828,RMVar_hsa_circ_312086,RMVar_hsa_circ_93465,RMVar_hsa_circ_152840,RMVar_hsa_circ_152841,RMVar_hsa_circ_40990,RMVar_hsa_circ_338567,RMVar_hsa_circ_152849,RMVar_hsa_circ_31863,RMVar_hsa_circ_108111,RMVar_hsa_circ_152851,RMVar_hsa_circ_265154,RMVar_hsa_circ_275286,RMVar_hsa_circ_152854,RMVar_hsa_circ_152856,RMVar_hsa_circ_306126,RMVar_hsa_circ_152855,RMVar_hsa_circ_152857,RMVar_hsa_circ_64267 26154 RMVar_ID_26154 Human_SNP_ID_480982526 A-to-I Human chr11 + 108097181 108097181 108097181 CTGGGACTACAGGTGCATGCCCCACGCTGGCTAATTTTTGTATTTTCAGTAGAGACGGGGTTTTG CTGGGACTACAGGTGCATGCCCCACGCTGGCTGATTTTTGTATTTTCAGTAGAGACGGGGTTTTG A G CUL5 Ensembl:ENSG00000166266 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs995673622 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33769,RMVar_hsa_circ_334417,RMVar_hsa_circ_152827,RMVar_hsa_circ_35432,RMVar_hsa_circ_152828,RMVar_hsa_circ_312086,RMVar_hsa_circ_93465,RMVar_hsa_circ_152840,RMVar_hsa_circ_152841,RMVar_hsa_circ_40990,RMVar_hsa_circ_338567,RMVar_hsa_circ_152849,RMVar_hsa_circ_31863,RMVar_hsa_circ_108111,RMVar_hsa_circ_152851,RMVar_hsa_circ_265154,RMVar_hsa_circ_275286,RMVar_hsa_circ_152854,RMVar_hsa_circ_152856,RMVar_hsa_circ_306126,RMVar_hsa_circ_152855,RMVar_hsa_circ_152857,RMVar_hsa_circ_64267 26155 RMVar_ID_26155 Human_SNP_ID_480982542 A-to-I Human chr11 + 108097236 108097236 108097236 CGGGGTTTTGCCGTGTTGCCCAGGCTGGTTTCAGACTCCTGAGCTCAAGTAATCTGCCTGCCTCA CGGGGTTTTGCCGTGTTGCCCAGGCTGGTTTCTGACTCCTGAGCTCAAGTAATCTGCCTGCCTCA A T CUL5 Ensembl:ENSG00000166266 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1302778652 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33769,RMVar_hsa_circ_334417,RMVar_hsa_circ_152827,RMVar_hsa_circ_35432,RMVar_hsa_circ_152828,RMVar_hsa_circ_312086,RMVar_hsa_circ_93465,RMVar_hsa_circ_152840,RMVar_hsa_circ_152841,RMVar_hsa_circ_40990,RMVar_hsa_circ_338567,RMVar_hsa_circ_152849,RMVar_hsa_circ_31863,RMVar_hsa_circ_108111,RMVar_hsa_circ_152851,RMVar_hsa_circ_265154,RMVar_hsa_circ_275286,RMVar_hsa_circ_152854,RMVar_hsa_circ_152856,RMVar_hsa_circ_306126,RMVar_hsa_circ_152855,RMVar_hsa_circ_152857,RMVar_hsa_circ_64267 26156 RMVar_ID_26156 Human_SNP_ID_480982548 A-to-I Human chr11 + 108097254 108097254 108097254 CCCAGGCTGGTTTCAGACTCCTGAGCTCAAGTAATCTGCCTGCCTCAGCTTCCCAAAGTGCTGGA CCCAGGCTGGTTTCAGACTCCTGAGCTCAAGTTATCTGCCTGCCTCAGCTTCCCAAAGTGCTGGA A T CUL5 Ensembl:ENSG00000166266 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1565270673 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33769,RMVar_hsa_circ_334417,RMVar_hsa_circ_152827,RMVar_hsa_circ_35432,RMVar_hsa_circ_152828,RMVar_hsa_circ_312086,RMVar_hsa_circ_93465,RMVar_hsa_circ_152840,RMVar_hsa_circ_152841,RMVar_hsa_circ_40990,RMVar_hsa_circ_338567,RMVar_hsa_circ_152849,RMVar_hsa_circ_31863,RMVar_hsa_circ_108111,RMVar_hsa_circ_152851,RMVar_hsa_circ_265154,RMVar_hsa_circ_275286,RMVar_hsa_circ_152854,RMVar_hsa_circ_152856,RMVar_hsa_circ_306126,RMVar_hsa_circ_152855,RMVar_hsa_circ_152857,RMVar_hsa_circ_64267 26157 RMVar_ID_26157 Human_SNP_ID_480999766 A-to-I Human chr11 - 108161973 108161973 108161973 TTCTGACAAAAGTATTGCCACAGATCTTGGGAAAAAATCAGAAGAAACCACAGTTCCCTTCCCAG TTCTGACAAAAGTATTGCCACAGATCTTGGGAGAAAATCAGAAGAAACCACAGTTCCCTTCCCAG T C NPAT Ensembl:ENSG00000149308 Protein coding CDS GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs758593922 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27614220 Human_Splice_Rec_1294700,Human_Splice_Rec_1294708,Human_Splice_Rec_1294710 RMVar_hsa_circ_21118,RMVar_hsa_circ_152873,RMVar_hsa_circ_79904,RMVar_hsa_circ_90354,RMVar_hsa_circ_152874,RMVar_hsa_circ_152875,RMVar_hsa_circ_152877,RMVar_hsa_circ_152878,RMVar_hsa_circ_152876,RMVar_hsa_circ_106452,RMVar_hsa_circ_152879 26158 RMVar_ID_26158 Human_SNP_ID_481000848 A-to-I Human chr11 - 108166058 108166058 108166058 GAGAAGACTTTGGGCACAATGGCTCCACTCCTATAATTCCAGCACTTTGGGAGGCCAAGACAGGT GAGAAGACTTTGGGCACAATGGCTCCACTCCTGTAATTCCAGCACTTTGGGAGGCCAAGACAGGT T C NPAT Ensembl:ENSG00000149308 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1276582399 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_152873,RMVar_hsa_circ_79904,RMVar_hsa_circ_90354,RMVar_hsa_circ_152874,RMVar_hsa_circ_152877,RMVar_hsa_circ_152878,RMVar_hsa_circ_152876,RMVar_hsa_circ_106452,RMVar_hsa_circ_267023,RMVar_hsa_circ_152879 26159 RMVar_ID_26159 Human_SNP_ID_481003870 A-to-I Human chr11 - 108177435 108177435 108177435 ATTATTCACGCTGAGTACAGTGGCCCACATCTATAATCCCAGTGCTCTGGGAGGCTGAGGCAAGA ATTATTCACGCTGAGTACAGTGGCCCACATCTGTAATCCCAGTGCTCTGGGAGGCTGAGGCAAGA T C NPAT Ensembl:ENSG00000149308 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs139576405 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9626706,Human_RBP_ID_11514619 RMVar_hsa_circ_90354,RMVar_hsa_circ_152874,RMVar_hsa_circ_152878,RMVar_hsa_circ_24929,RMVar_hsa_circ_27190,RMVar_hsa_circ_269452,RMVar_hsa_circ_124885,RMVar_hsa_circ_152883,RMVar_hsa_circ_319318,RMVar_hsa_circ_312774,RMVar_hsa_circ_71581,RMVar_hsa_circ_152888,RMVar_hsa_circ_6956,RMVar_hsa_circ_152887,RMVar_hsa_circ_276486,RMVar_hsa_circ_352000,RMVar_hsa_circ_354167,RMVar_hsa_circ_315893,RMVar_hsa_circ_152890,RMVar_hsa_circ_152891,RMVar_hsa_circ_333792 26160 RMVar_ID_26160 Human_SNP_ID_481003871 A-to-I Human chr11 - 108177439 108177439 108177439 TCATATTATTCACGCTGAGTACAGTGGCCCACATCTATAATCCCAGTGCTCTGGGAGGCTGAGGC TCATATTATTCACGCTGAGTACAGTGGCCCACGTCTATAATCCCAGTGCTCTGGGAGGCTGAGGC T C NPAT Ensembl:ENSG00000149308 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1228577808 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11514619 RMVar_hsa_circ_90354,RMVar_hsa_circ_152874,RMVar_hsa_circ_152878,RMVar_hsa_circ_24929,RMVar_hsa_circ_27190,RMVar_hsa_circ_269452,RMVar_hsa_circ_124885,RMVar_hsa_circ_152883,RMVar_hsa_circ_319318,RMVar_hsa_circ_312774,RMVar_hsa_circ_71581,RMVar_hsa_circ_152888,RMVar_hsa_circ_6956,RMVar_hsa_circ_152887,RMVar_hsa_circ_276486,RMVar_hsa_circ_352000,RMVar_hsa_circ_354167,RMVar_hsa_circ_315893,RMVar_hsa_circ_152890,RMVar_hsa_circ_152891,RMVar_hsa_circ_333792 26161 RMVar_ID_26161 Human_SNP_ID_481004483 A-to-I Human chr11 - 108180097 108180097 108180097 ATCTAGAACTCCTGGGCTCAAGTGATCTCCCCACTTCAGCCTCTCAAAGTGCTAGGACTATAGGT ATCTAGAACTCCTGGGCTCAAGTGATCTCCCCGCTTCAGCCTCTCAAAGTGCTAGGACTATAGGT T C NPAT Ensembl:ENSG00000149308 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1442080781 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90354,RMVar_hsa_circ_152874,RMVar_hsa_circ_152878,RMVar_hsa_circ_24929,RMVar_hsa_circ_27190,RMVar_hsa_circ_269452,RMVar_hsa_circ_124885,RMVar_hsa_circ_152883,RMVar_hsa_circ_319318,RMVar_hsa_circ_312774,RMVar_hsa_circ_71581,RMVar_hsa_circ_152888,RMVar_hsa_circ_6956,RMVar_hsa_circ_152887,RMVar_hsa_circ_276486,RMVar_hsa_circ_352000,RMVar_hsa_circ_354167,RMVar_hsa_circ_315893,RMVar_hsa_circ_152890,RMVar_hsa_circ_152891,RMVar_hsa_circ_333792 26162 RMVar_ID_26162 Human_SNP_ID_481004530 A-to-I Human chr11 - 108180281 108180281 108180281 GCTGCATGCCCAGGCTGGAGTGATGTGGTGCAATCTTGGCTCACTGCAGCCTGAACCTCTTTGAG GCTGCATGCCCAGGCTGGAGTGATGTGGTGCAGTCTTGGCTCACTGCAGCCTGAACCTCTTTGAG T C NPAT Ensembl:ENSG00000149308 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs761557985 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90354,RMVar_hsa_circ_152874,RMVar_hsa_circ_152878,RMVar_hsa_circ_24929,RMVar_hsa_circ_27190,RMVar_hsa_circ_269452,RMVar_hsa_circ_124885,RMVar_hsa_circ_152883,RMVar_hsa_circ_319318,RMVar_hsa_circ_312774,RMVar_hsa_circ_71581,RMVar_hsa_circ_152888,RMVar_hsa_circ_6956,RMVar_hsa_circ_152887,RMVar_hsa_circ_276486,RMVar_hsa_circ_352000,RMVar_hsa_circ_354167,RMVar_hsa_circ_315893,RMVar_hsa_circ_152890,RMVar_hsa_circ_152891,RMVar_hsa_circ_333792 26163 RMVar_ID_26163 Human_SNP_ID_481004802 A-to-I Human chr11 - 108181443 108181435 108181443 TTGTTTTTTTTGAGACAGAGTCTCGCTCTGTCACCCTGGCTGGAATGCAGTGGTGTGATCTCAGC TTGTTTTTTTTGAGACAGAGTCTCGCTCTGTC________TGGAATGCAGTGGTGTGATCTCAGC AGCCAGGGT A NPAT Ensembl:ENSG00000149308 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1018762684 Functional Loss DEL dbSNP153 33..40 33 - - - Human_RBP_ID_11514676,Human_RBP_ID_22570145 RMVar_hsa_circ_90354,RMVar_hsa_circ_152874,RMVar_hsa_circ_152878,RMVar_hsa_circ_24929,RMVar_hsa_circ_27190,RMVar_hsa_circ_269452,RMVar_hsa_circ_124885,RMVar_hsa_circ_152883,RMVar_hsa_circ_319318,RMVar_hsa_circ_312774,RMVar_hsa_circ_71581,RMVar_hsa_circ_152888,RMVar_hsa_circ_6956,RMVar_hsa_circ_152887,RMVar_hsa_circ_276486,RMVar_hsa_circ_352000,RMVar_hsa_circ_354167,RMVar_hsa_circ_315893,RMVar_hsa_circ_152890,RMVar_hsa_circ_152891,RMVar_hsa_circ_333792 26164 RMVar_ID_26164 Human_SNP_ID_481005350 A-to-I Human chr11 - 108183702 108183702 108183702 CAACTCCTGAGTTCAAACGATTCTCCTGCCTCAGCTTCCCAAGTAGCTGGGATTATAGGCATGCA CAACTCCTGAGTTCAAACGATTCTCCTGCCTCGGCTTCCCAAGTAGCTGGGATTATAGGCATGCA T C NPAT Ensembl:ENSG00000149308 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1250067950 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24865884 RMVar_hsa_circ_90354,RMVar_hsa_circ_152874,RMVar_hsa_circ_152878,RMVar_hsa_circ_24929,RMVar_hsa_circ_27190,RMVar_hsa_circ_269452,RMVar_hsa_circ_124885,RMVar_hsa_circ_152883,RMVar_hsa_circ_319318,RMVar_hsa_circ_312774,RMVar_hsa_circ_71581,RMVar_hsa_circ_152888,RMVar_hsa_circ_6956,RMVar_hsa_circ_152887,RMVar_hsa_circ_276486,RMVar_hsa_circ_352000,RMVar_hsa_circ_354167,RMVar_hsa_circ_315893,RMVar_hsa_circ_152890,RMVar_hsa_circ_152891,RMVar_hsa_circ_333792 26165 RMVar_ID_26165 Human_SNP_ID_481005369 A-to-I Human chr11 - 108183773 108183773 108183773 TTTTGTTTTTTGAGGTGGTGTCTCGCTGTGTCACCCAGGCTGGAGTGCAGTGGCACGATCTTGGC TTTTGTTTTTTGAGGTGGTGTCTCGCTGTGTCGCCCAGGCTGGAGTGCAGTGGCACGATCTTGGC T C NPAT Ensembl:ENSG00000149308 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1893812 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2590,GWAS_ID_2591,GWAS_ID_2592,GWAS_ID_2593,GWAS_ID_2594,GWAS_ID_2595,GWAS_ID_2596,GWAS_ID_2597,GWAS_ID_2598,GWAS_ID_2599,GWAS_ID_2600,GWAS_ID_2601,GWAS_ID_2602,GWAS_ID_2603,GWAS_ID_2604,GWAS_ID_2605,GWAS_ID_2606,GWAS_ID_2607,GWAS_ID_2608,GWAS_ID_2609,GWAS_ID_2610,GWAS_ID_2611,GWAS_ID_2612 RMVar_hsa_circ_90354,RMVar_hsa_circ_152874,RMVar_hsa_circ_152878,RMVar_hsa_circ_24929,RMVar_hsa_circ_27190,RMVar_hsa_circ_269452,RMVar_hsa_circ_124885,RMVar_hsa_circ_152883,RMVar_hsa_circ_319318,RMVar_hsa_circ_312774,RMVar_hsa_circ_71581,RMVar_hsa_circ_152888,RMVar_hsa_circ_6956,RMVar_hsa_circ_152887,RMVar_hsa_circ_276486,RMVar_hsa_circ_352000,RMVar_hsa_circ_354167,RMVar_hsa_circ_315893,RMVar_hsa_circ_152890,RMVar_hsa_circ_152891,RMVar_hsa_circ_333792 26166 RMVar_ID_26166 Human_SNP_ID_481005607 A-to-I Human chr11 - 108184566 108184566 108184566 GGATCGCACCACTGCTCTCCAGCCTGGGTGACAGAGCAAGACCCTGTCTCAAAAAAATAAGAAAA GGATCGCACCACTGCTCTCCAGCCTGGGTGACGGAGCAAGACCCTGTCTCAAAAAAATAAGAAAA T C NPAT Ensembl:ENSG00000149308 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1034268175 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90354,RMVar_hsa_circ_152874,RMVar_hsa_circ_152878,RMVar_hsa_circ_24929,RMVar_hsa_circ_27190,RMVar_hsa_circ_269452,RMVar_hsa_circ_124885,RMVar_hsa_circ_152883,RMVar_hsa_circ_319318,RMVar_hsa_circ_312774,RMVar_hsa_circ_71581,RMVar_hsa_circ_152888,RMVar_hsa_circ_6956,RMVar_hsa_circ_152887,RMVar_hsa_circ_276486,RMVar_hsa_circ_352000,RMVar_hsa_circ_354167,RMVar_hsa_circ_315893,RMVar_hsa_circ_152890,RMVar_hsa_circ_152891,RMVar_hsa_circ_333792 26167 RMVar_ID_26167 Human_SNP_ID_481011160 A-to-I Human chr11 - 108205421 108205421 108205421 TCTCTATTAAAAATTTTTTCATTTAATTAGCCAGGCATAGTTGTGAGTTCCTGTCATCCCAGCTA TCTCTATTAAAAATTTTTTCATTTAATTAGCCGGGCATAGTTGTGAGTTCCTGTCATCCCAGCTA T C NPAT Ensembl:ENSG00000149308 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1229159785 Functional Loss SNV dbSNP153 33..33 33 - - - 26168 RMVar_ID_26168 Human_SNP_ID_481013565 A-to-I Human chr11 - 108213980 108213980 108213980 GGTTGGCTGAAGTGGGAGGATCACTTCAGCCCAGGAGTTCAAGGTTATAGTGAGCTATGATTGAG GGTTGGCTGAAGTGGGAGGATCACTTCAGCCCCGGAGTTCAAGGTTATAGTGAGCTATGATTGAG T G NPAT Ensembl:ENSG00000149308 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1428171338 Functional Loss SNV dbSNP153 33..33 33 - - - 26169 RMVar_ID_26169 Human_SNP_ID_481018352 A-to-I Human chr11 + 108231525 108231525 108231525 CGAGACCAGCCTGGCCAATATAGCGAAACCCCATCTCTACTAAAAGTACAAAAAATAGCTGGGTG CGAGACCAGCCTGGCCAATATAGCGAAACCCCGTCTCTACTAAAAGTACAAAAAATAGCTGGGTG A G ATM Ensembl:ENSG00000149311 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1404077047 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6801,RMVar_hsa_circ_90159,RMVar_hsa_circ_152901,RMVar_hsa_circ_106305,RMVar_hsa_circ_356691,RMVar_hsa_circ_55016,RMVar_hsa_circ_73598,RMVar_hsa_circ_270547,RMVar_hsa_circ_299267,RMVar_hsa_circ_312549,RMVar_hsa_circ_332985,RMVar_hsa_circ_152902,RMVar_hsa_circ_330255,RMVar_hsa_circ_299791,RMVar_hsa_circ_296222,RMVar_hsa_circ_278926,RMVar_hsa_circ_280158,RMVar_hsa_circ_276431,RMVar_hsa_circ_113339,RMVar_hsa_circ_116643,RMVar_hsa_circ_121942,RMVar_hsa_circ_115337,RMVar_hsa_circ_108066,RMVar_hsa_circ_91728,RMVar_hsa_circ_43362,RMVar_hsa_circ_51406,RMVar_hsa_circ_60403,RMVar_hsa_circ_44771,RMVar_hsa_circ_34991,RMVar_hsa_circ_35781,RMVar_hsa_circ_32037,RMVar_hsa_circ_57476,RMVar_hsa_circ_152908,RMVar_hsa_circ_152912,RMVar_hsa_circ_152914,RMVar_hsa_circ_152916,RMVar_hsa_circ_152915,RMVar_hsa_circ_152913,RMVar_hsa_circ_152910,RMVar_hsa_circ_152911,RMVar_hsa_circ_152909,RMVar_hsa_circ_152904,RMVar_hsa_circ_152906,RMVar_hsa_circ_152907,RMVar_hsa_circ_152905,RMVar_hsa_circ_63348,RMVar_hsa_circ_364167,RMVar_hsa_circ_152903,RMVar_hsa_circ_351034,RMVar_hsa_circ_288989,RMVar_hsa_circ_59359,RMVar_hsa_circ_105798,RMVar_hsa_circ_152921 26170 RMVar_ID_26170 Human_SNP_ID_481040473 A-to-I Human chr11 + 108305433 108305433 108305433 GAAACCCCGTCCCTACTAAAAATACAAAAATTAGCCGGGCATGGTGGCAGGCGCCTATAATTGCA GAAACCCCGTCCCTACTAAAAATACAAAAATTGGCCGGGCATGGTGGCAGGCGCCTATAATTGCA A G ATM Ensembl:ENSG00000149311 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1028251767 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6801,RMVar_hsa_circ_299267,RMVar_hsa_circ_280158,RMVar_hsa_circ_113339,RMVar_hsa_circ_116643,RMVar_hsa_circ_115337,RMVar_hsa_circ_35781,RMVar_hsa_circ_152904,RMVar_hsa_circ_152905,RMVar_hsa_circ_152903,RMVar_hsa_circ_7225,RMVar_hsa_circ_41294,RMVar_hsa_circ_106877,RMVar_hsa_circ_152940,RMVar_hsa_circ_123221,RMVar_hsa_circ_7748,RMVar_hsa_circ_152950,RMVar_hsa_circ_32076,RMVar_hsa_circ_31637,RMVar_hsa_circ_49737,RMVar_hsa_circ_339703,RMVar_hsa_circ_107462,RMVar_hsa_circ_152954,RMVar_hsa_circ_89180,RMVar_hsa_circ_119781,RMVar_hsa_circ_50318,RMVar_hsa_circ_67517,RMVar_hsa_circ_152956,RMVar_hsa_circ_152957,RMVar_hsa_circ_344580,RMVar_hsa_circ_50841,RMVar_hsa_circ_152965,RMVar_hsa_circ_88369,RMVar_hsa_circ_152961,RMVar_hsa_circ_15980,RMVar_hsa_circ_125610,RMVar_hsa_circ_75498,RMVar_hsa_circ_152966,RMVar_hsa_circ_152968,RMVar_hsa_circ_55975,RMVar_hsa_circ_347105,RMVar_hsa_circ_366809,RMVar_hsa_circ_368220,RMVar_hsa_circ_377267,RMVar_hsa_circ_352673,RMVar_hsa_circ_312896,RMVar_hsa_circ_285836,RMVar_hsa_circ_152970,RMVar_hsa_circ_152971,RMVar_hsa_circ_152969,RMVar_hsa_circ_339493,RMVar_hsa_circ_356426,RMVar_hsa_circ_362672,RMVar_hsa_circ_349462,RMVar_hsa_circ_296600,RMVar_hsa_circ_276757,RMVar_hsa_circ_38509,RMVar_hsa_circ_322755,RMVar_hsa_circ_152973,RMVar_hsa_circ_152974,RMVar_hsa_circ_152975,RMVar_hsa_circ_368854,RMVar_hsa_circ_339858,RMVar_hsa_circ_302450,RMVar_hsa_circ_275497,RMVar_hsa_circ_152976,RMVar_hsa_circ_152978,RMVar_hsa_circ_152979,RMVar_hsa_circ_152977,RMVar_hsa_circ_70054 26171 RMVar_ID_26171 Human_SNP_ID_481040485 A-to-I Human chr11 + 108305457 108305457 108305457 CAAAAATTAGCCGGGCATGGTGGCAGGCGCCTATAATTGCAGCTACTTGGGAGGCTGAGGCAGGA CAAAAATTAGCCGGGCATGGTGGCAGGCGCCTGTAATTGCAGCTACTTGGGAGGCTGAGGCAGGA A G ATM Ensembl:ENSG00000149311 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs532558935 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6801,RMVar_hsa_circ_299267,RMVar_hsa_circ_280158,RMVar_hsa_circ_113339,RMVar_hsa_circ_116643,RMVar_hsa_circ_115337,RMVar_hsa_circ_35781,RMVar_hsa_circ_152904,RMVar_hsa_circ_152905,RMVar_hsa_circ_152903,RMVar_hsa_circ_7225,RMVar_hsa_circ_41294,RMVar_hsa_circ_106877,RMVar_hsa_circ_152940,RMVar_hsa_circ_123221,RMVar_hsa_circ_7748,RMVar_hsa_circ_152950,RMVar_hsa_circ_32076,RMVar_hsa_circ_31637,RMVar_hsa_circ_49737,RMVar_hsa_circ_339703,RMVar_hsa_circ_107462,RMVar_hsa_circ_152954,RMVar_hsa_circ_89180,RMVar_hsa_circ_119781,RMVar_hsa_circ_50318,RMVar_hsa_circ_67517,RMVar_hsa_circ_152956,RMVar_hsa_circ_152957,RMVar_hsa_circ_344580,RMVar_hsa_circ_50841,RMVar_hsa_circ_152965,RMVar_hsa_circ_88369,RMVar_hsa_circ_152961,RMVar_hsa_circ_15980,RMVar_hsa_circ_125610,RMVar_hsa_circ_75498,RMVar_hsa_circ_152966,RMVar_hsa_circ_152968,RMVar_hsa_circ_55975,RMVar_hsa_circ_347105,RMVar_hsa_circ_366809,RMVar_hsa_circ_368220,RMVar_hsa_circ_377267,RMVar_hsa_circ_352673,RMVar_hsa_circ_312896,RMVar_hsa_circ_285836,RMVar_hsa_circ_152970,RMVar_hsa_circ_152971,RMVar_hsa_circ_152969,RMVar_hsa_circ_339493,RMVar_hsa_circ_356426,RMVar_hsa_circ_362672,RMVar_hsa_circ_349462,RMVar_hsa_circ_296600,RMVar_hsa_circ_276757,RMVar_hsa_circ_38509,RMVar_hsa_circ_322755,RMVar_hsa_circ_152973,RMVar_hsa_circ_152974,RMVar_hsa_circ_152975,RMVar_hsa_circ_368854,RMVar_hsa_circ_339858,RMVar_hsa_circ_302450,RMVar_hsa_circ_275497,RMVar_hsa_circ_152976,RMVar_hsa_circ_152978,RMVar_hsa_circ_152979,RMVar_hsa_circ_152977,RMVar_hsa_circ_70054 26172 RMVar_ID_26172 Human_SNP_ID_481057157 A-to-I Human chr11 + 108365786 108365786 108365786 CTGTAATCCCAGCACTTTGGGAGGCCGAGGTGAGCGGATCACAAGGTCAGGAGTTCGAGACCAGC CTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGCGGATCACAAGGTCAGGAGTTCGAGACCAGC A G ATM Ensembl:ENSG00000149311 Protein coding 3'UTR GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs929413948 Functional Loss SNV dbSNP153 33..33 33 - - - 26173 RMVar_ID_26173 Human_SNP_ID_481057162 A-to-I Human chr11 + 108365796 108365796 108365796 AGCACTTTGGGAGGCCGAGGTGAGCGGATCACAAGGTCAGGAGTTCGAGACCAGCCTGGCCAAGA AGCACTTTGGGAGGCCGAGGTGAGCGGATCACGAGGTCAGGAGTTCGAGACCAGCCTGGCCAAGA A G ATM Ensembl:ENSG00000149311 Protein coding 3'UTR GSE47997;GSE38233;GSE38233;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;cultured B-cells;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,24183664,32596459 RNA-Seq:(High) rs867513306 Functional Loss SNV dbSNP153 33..33 33 - - - 26174 RMVar_ID_26174 Human_SNP_ID_481057189 A-to-I Human chr11 + 108365935 108365935 108365935 CCTGTAATCCCAGCTACTCGAGAGGCTGAGGCAGGAGAATCTCTTGAACCTGGGAGGTGAAGGTT CCTGTAATCCCAGCTACTCGAGAGGCTGAGGCTGGAGAATCTCTTGAACCTGGGAGGTGAAGGTT A T ATM Ensembl:ENSG00000149311 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1216620155 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11516526 26175 RMVar_ID_26175 Human_SNP_ID_481057466 A-to-I Human chr11 + 108367129 108367129 108367129 CCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGTGTGCCAACACGCCCGGCTAATTTTTTG CCTGCCTCAGCCTCCCGAGTAGCTGGGACTACGGGCGTGTGCCAACACGCCCGGCTAATTTTTTG A G ATM Ensembl:ENSG00000149311 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1393415054 Functional Loss SNV dbSNP153 33..33 33 - - - 26176 RMVar_ID_26176 Human_SNP_ID_481057506 A-to-I Human chr11 + 108367248 108367248 108367248 TGACCTCGTGATCCACCCTCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCGC TGACCTCGTGATCCACCCTCCTCGGCCTCCCATAGTGCTGGGATTACAGGTGTGAGCCACCGCGC A T ATM Ensembl:ENSG00000149311 Protein coding 3'UTR GSE38233;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29796672,31158229,32596459 RNA-Seq:(High) rs886161195 Functional Loss SNV dbSNP153 33..33 33 - - - 26177 RMVar_ID_26177 Human_SNP_ID_481075952 A-to-I Human chr11 - 108437621 108437621 108437621 ACTGCAACCTCTGCCTCTGCCTCCCGGATTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCT ACTGCAACCTCTGCCTCTGCCTCCCGGATTCAGGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCT T C C11orf65 Ensembl:ENSG00000166323 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs891935981 Functional Loss SNV dbSNP153 33..33 33 - - - 26178 RMVar_ID_26178 Human_SNP_ID_481099494 A-to-I Human chr11 - 108526198 108526198 108526198 AAGAGAGAGGCTGGGAAGAGTGGTTCATGCCTATAATCTCAACACTTTGGGAGGCCAAGGTGGGA AAGAGAGAGGCTGGGAAGAGTGGTTCATGCCTGTAATCTCAACACTTTGGGAGGCCAAGGTGGGA T C EXPH5 Ensembl:ENSG00000110723 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs189242915 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265894,RMVar_hsa_circ_365186 26179 RMVar_ID_26179 Human_SNP_ID_481108729 A-to-I Human chr11 - 108564062 108564062 108564062 TTGGCCAGGCTGACCTCGAACTCCTGACCTCAAGTGATCCGTCCGCCTCAGCCTCCCAAAGTTCT TTGGCCAGGCTGACCTCGAACTCCTGACCTCACGTGATCCGTCCGCCTCAGCCTCCCAAAGTTCT T G EXPH5 Ensembl:ENSG00000110723 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs930707044 Functional Loss SNV dbSNP153 33..33 33 - - - 26180 RMVar_ID_26180 Human_SNP_ID_481108970 A-to-I Human chr11 - 108565094 108565094 108565094 TGACACCAGCCTGGCCAACATGATGAAACCCCATCTCTACTAAAAATACAAAAATTAGCCAGGCG TGACACCAGCCTGGCCAACATGATGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCCAGGCG T C EXPH5 Ensembl:ENSG00000110723 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1168444633 Functional Loss SNV dbSNP153 33..33 33 - - - 26181 RMVar_ID_26181 Human_SNP_ID_481149097 A-to-I Human chr11 + 108728608 108728608 108728608 ATGATTGTGGCTCACTGTACCCCCAAACTCCCAGGCCCAAGCGATTCTTCTGCCCTAGCCTCCTG ATGATTGTGGCTCACTGTACCCCCAAACTCCCGGGCCCAAGCGATTCTTCTGCCCTAGCCTCCTG A G DDX10 Ensembl:ENSG00000178105 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264320901 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11517674 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 26182 RMVar_ID_26182 Human_SNP_ID_481154751 A-to-I Human chr11 + 108751835 108751835 108751835 TTTAAGTCGACTGTATAACTGTCTTTCAGTCTAAATCACACCTGCTTATTTAGTACTAAGTAAGC TTTAAGTCGACTGTATAACTGTCTTTCAGTCTGAATCACACCTGCTTATTTAGTACTAAGTAAGC A G DDX10 Ensembl:ENSG00000178105 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1164095082 Functional Loss SNV dbSNP153 33..33 33 - - - 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 26183 RMVar_ID_26183 Human_SNP_ID_663057899 A-to-I Human chr19 + 30012406 30012406 30012406 CTAGTGAAAGCAGTGCTGCTGAATTTGATGATAGGCGGGGAGTTTTGAGGAGTATCAGCTGCGAA CTAGTGAAAGCAGTGCTGCTGAATTTGATGATGGGCGGGGAGTTTTGAGGAGTATCAGCTGCGAA A G URI1 Ensembl:ENSG00000105176 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1043876 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1882951,Human_RBP_ID_8831507,Human_RBP_ID_9380875,Human_RBP_ID_13421762,Human_RBP_ID_17919542,Human_RBP_ID_18727053,Human_RBP_ID_22071931,Human_RBP_ID_23790455,Human_RBP_ID_24545587,Human_RBP_ID_26334898,Human_RBP_ID_27815349 Human_miRNA_ID_240633,Human_miRNA_ID_1732109,Human_miRNA_ID_2033206,Human_miRNA_ID_2888146 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_3099,RMVar_hsa_circ_67468,RMVar_hsa_circ_278882,RMVar_hsa_circ_193827,RMVar_hsa_circ_193828,RMVar_hsa_circ_59159,RMVar_hsa_circ_333992 26184 RMVar_ID_26184 Human_SNP_ID_663058716 A-to-I Human chr19 + 30015559 30015559 30015559 CTCTTGTAGGTTTTGCGGCTAGTTGGCTATTCAAGAAACCTCGCCCCTCTGAATGTCATACTGTA CTCTTGTAGGTTTTGCGGCTAGTTGGCTATTCTAGAAACCTCGCCCCTCTGAATGTCATACTGTA A T URI1 Ensembl:ENSG00000105176 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1482959904 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_518775,Human_RBP_ID_1014387,Human_RBP_ID_1239793,Human_RBP_ID_1558961,Human_RBP_ID_1882985,Human_RBP_ID_3567079,Human_RBP_ID_4565405,Human_RBP_ID_8482489,Human_RBP_ID_8831525,Human_RBP_ID_13421887,Human_RBP_ID_17498653,Human_RBP_ID_17919574,Human_RBP_ID_23790502 Human_Splice_Rec_1987856 Human_miRNA_ID_1689801 RMVar_hsa_circ_193825,RMVar_hsa_circ_193826 26185 RMVar_ID_26185 Human_SNP_ID_663065671 A-to-I Human chr19 + 30041308 30041308 30041308 AGGGTGGTGCATTCCTGCAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAACCAG AGGGTGGTGCATTCCTGCAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCTTGAACCAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs933089941 Functional Loss SNV dbSNP153 33..33 33 - - - 26186 RMVar_ID_26186 Human_SNP_ID_663693555 A-to-I Human chr19 + 32427215 32427215 32427215 CTGGGTCTTGCCATGTTGCCTAGGCTGGTCTTAAAGTCCTGGGCTTAAGTAATCCACCTACCTCG CTGGGTCTTGCCATGTTGCCTAGGCTGGTCTTGAAGTCCTGGGCTTAAGTAATCCACCTACCTCG A G DPY19L3 Ensembl:ENSG00000178904 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs565023316 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22940,RMVar_hsa_circ_117874,RMVar_hsa_circ_193851,RMVar_hsa_circ_121877,RMVar_hsa_circ_193855,RMVar_hsa_circ_113426,RMVar_hsa_circ_193852,RMVar_hsa_circ_116334,RMVar_hsa_circ_193856 26187 RMVar_ID_26187 Human_SNP_ID_663700904 A-to-I Human chr19 + 32455194 32455194 32455194 GTTTCCTAGGCTGGCCTTGAACACCTGGTCTCAGATGGCCCTCCCACCTTAGCCTCCCAAGTTGC GTTTCCTAGGCTGGCCTTGAACACCTGGTCTCCGATGGCCCTCCCACCTTAGCCTCCCAAGTTGC A C DPY19L3 Ensembl:ENSG00000178904 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1208095405 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22940,RMVar_hsa_circ_319059,RMVar_hsa_circ_330176,RMVar_hsa_circ_193858,RMVar_hsa_circ_5484,RMVar_hsa_circ_193859,RMVar_hsa_circ_9825,RMVar_hsa_circ_341401,RMVar_hsa_circ_362564,RMVar_hsa_circ_56188 26188 RMVar_ID_26188 Human_SNP_ID_663734527 A-to-I Human chr19 + 32583781 32583781 32583781 CACAGGAGCTTGAGCTGATCATAGCTGCAGTGAGCTGTGATTGCACCACTGTACTCCAGCATGAA CACAGGAGCTTGAGCTGATCATAGCTGCAGTGTGCTGTGATTGCACCACTGTACTCCAGCATGAA A T PDCD5 Ensembl:ENSG00000105185 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1444988206 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1559350,Human_RBP_ID_17568025 RMVar_hsa_circ_76035,RMVar_hsa_circ_97698,RMVar_hsa_circ_193864,RMVar_hsa_circ_193866 26189 RMVar_ID_26189 Human_SNP_ID_663734569 A-to-I Human chr19 + 32583971 32583971 32583971 CTCCTGCCTCTGCCTCCCAAGTAGCTGGGATTACAGGCACCCGCCACCATGCCCGGCTAATTTTT CTCCTGCCTCTGCCTCCCAAGTAGCTGGGATTGCAGGCACCCGCCACCATGCCCGGCTAATTTTT A G PDCD5 Ensembl:ENSG00000105185 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1416547208 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76035,RMVar_hsa_circ_97698,RMVar_hsa_circ_193864,RMVar_hsa_circ_193866 26190 RMVar_ID_26190 Human_SNP_ID_663750739 A-to-I Human chr19 - 32640889 32640889 32640889 GTTTCAAAAACAAACAAACAAAAAAAAGAGACAGGGTCTCACTCTGTCACCCAGGCTGGGTGCAT GTTTCAAAAACAAACAAACAAAAAAAAGAGACGGGGTCTCACTCTGTCACCCAGGCTGGGTGCAT T C ANKRD27 Ensembl:ENSG00000105186 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1022032341 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126745,RMVar_hsa_circ_78380,RMVar_hsa_circ_193874,RMVar_hsa_circ_193875,RMVar_hsa_circ_326869,RMVar_hsa_circ_50075,RMVar_hsa_circ_305450,RMVar_hsa_circ_86158,RMVar_hsa_circ_78409,RMVar_hsa_circ_193886,RMVar_hsa_circ_193887,RMVar_hsa_circ_372620,RMVar_hsa_circ_295695,RMVar_hsa_circ_193894,RMVar_hsa_circ_193895,RMVar_hsa_circ_285723,RMVar_hsa_circ_11015,RMVar_hsa_circ_91625,RMVar_hsa_circ_334357,RMVar_hsa_circ_104569,RMVar_hsa_circ_193906,RMVar_hsa_circ_325481,RMVar_hsa_circ_289199,RMVar_hsa_circ_295130,RMVar_hsa_circ_108993,RMVar_hsa_circ_1108,RMVar_hsa_circ_113531,RMVar_hsa_circ_193910,RMVar_hsa_circ_193912,RMVar_hsa_circ_193913,RMVar_hsa_circ_193911,RMVar_hsa_circ_47617,RMVar_hsa_circ_126103,RMVar_hsa_circ_14059,RMVar_hsa_circ_66275,RMVar_hsa_circ_282076,RMVar_hsa_circ_14031,RMVar_hsa_circ_193918,RMVar_hsa_circ_193919,RMVar_hsa_circ_316605,RMVar_hsa_circ_273399,RMVar_hsa_circ_100968,RMVar_hsa_circ_121903,RMVar_hsa_circ_193922,RMVar_hsa_circ_193923,RMVar_hsa_circ_193921,RMVar_hsa_circ_48534,RMVar_hsa_circ_193925,RMVar_hsa_circ_69867,RMVar_hsa_circ_41633,RMVar_hsa_circ_9762,RMVar_hsa_circ_193927,RMVar_hsa_circ_193928,RMVar_hsa_circ_48066,RMVar_hsa_circ_375478 26191 RMVar_ID_26191 Human_SNP_ID_663752091 A-to-I Human chr19 - 32645329 32645329 32645329 TGGCTCACTGCAGCCTCCAGCTCCCGGGTTCAAGCGATTCTCCTGTCTCAGCCTCCTGAGTAGCG TGGCTCACTGCAGCCTCCAGCTCCCGGGTTCAGGCGATTCTCCTGTCTCAGCCTCCTGAGTAGCG T C ANKRD27 Ensembl:ENSG00000105186 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs572359144 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78380,RMVar_hsa_circ_193875,RMVar_hsa_circ_372620,RMVar_hsa_circ_193895,RMVar_hsa_circ_91625,RMVar_hsa_circ_1108,RMVar_hsa_circ_113531,RMVar_hsa_circ_193910,RMVar_hsa_circ_66275,RMVar_hsa_circ_193919,RMVar_hsa_circ_316605,RMVar_hsa_circ_48534,RMVar_hsa_circ_2448,RMVar_hsa_circ_23999,RMVar_hsa_circ_9762,RMVar_hsa_circ_193927,RMVar_hsa_circ_193928,RMVar_hsa_circ_48066,RMVar_hsa_circ_375478,RMVar_hsa_circ_14092,RMVar_hsa_circ_299335,RMVar_hsa_circ_105519,RMVar_hsa_circ_107403,RMVar_hsa_circ_193933,RMVar_hsa_circ_193932,RMVar_hsa_circ_193937,RMVar_hsa_circ_193939,RMVar_hsa_circ_306393,RMVar_hsa_circ_308597,RMVar_hsa_circ_294720,RMVar_hsa_circ_193938 26192 RMVar_ID_26192 Human_SNP_ID_663752853 A-to-I Human chr19 - 32648252 32648248 32648252 TACATTTTTTTTTTCTTTTGAGGCGGAGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTAGCTTG TACATTTTTTTTTTCTTTTGAGGCGGAGTCTC____TGTCACCCAGGCTGGAGTGCAGTAGCTTG AGAGT A ANKRD27 Ensembl:ENSG00000105186 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs539410588 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_78380,RMVar_hsa_circ_193875,RMVar_hsa_circ_91625,RMVar_hsa_circ_1108,RMVar_hsa_circ_113531,RMVar_hsa_circ_193910,RMVar_hsa_circ_193919,RMVar_hsa_circ_316605,RMVar_hsa_circ_48534,RMVar_hsa_circ_2448,RMVar_hsa_circ_193927,RMVar_hsa_circ_193928,RMVar_hsa_circ_375478,RMVar_hsa_circ_14092,RMVar_hsa_circ_105519,RMVar_hsa_circ_107403,RMVar_hsa_circ_193933,RMVar_hsa_circ_193932,RMVar_hsa_circ_193939,RMVar_hsa_circ_306393,RMVar_hsa_circ_308597,RMVar_hsa_circ_193938,RMVar_hsa_circ_193940,RMVar_hsa_circ_346588 26193 RMVar_ID_26193 Human_SNP_ID_663764658 A-to-I Human chr19 - 32690120 32690120 32690120 TTACTGCAATATCTGCCTCTCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCTGGAGTAGCTGGGA TTACTGCAATATCTGCCTCTCGGGTTCAAGCAGTTCTCCTGCCTCAGCCTCTGGAGTAGCTGGGA T C AC008736.1 Ensembl:ENSG00000267475 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1275960162 Functional Loss SNV dbSNP153 33..33 33 - - - 26194 RMVar_ID_26194 Human_SNP_ID_663764659 A-to-I Human chr19 - 32690124 32690124 32690124 CGGCTTACTGCAATATCTGCCTCTCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCTGGAGTAGCT CGGCTTACTGCAATATCTGCCTCTCGGGTTCAGGCAATTCTCCTGCCTCAGCCTCTGGAGTAGCT T C AC008736.1 Ensembl:ENSG00000267475 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1284151442 Functional Loss SNV dbSNP153 33..33 33 - - - 26195 RMVar_ID_26195 Human_SNP_ID_663768274 A-to-I Human chr19 + 32700711 32700711 32700711 TTCAGCCTCCCAAAGTCTTGGGGATTATTGGCATAAGCTACTGTGCCTGGCCAGTTTCAGTCTTT TTCAGCCTCCCAAAGTCTTGGGGATTATTGGCGTAAGCTACTGTGCCTGGCCAGTTTCAGTCTTT A G NUDT19 Ensembl:ENSG00000213965 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs972119911 Functional Loss SNV dbSNP153 33..33 33 - - - 26196 RMVar_ID_26196 Human_SNP_ID_663768440 A-to-I Human chr19 + 32701305 32701305 32701305 TTGGCTCACTGAAACCTCTGCCTCCCAGGTTCAAGCGATTCTCCTTCCTCAGTCTCCCAAGCAGC TTGGCTCACTGAAACCTCTGCCTCCCAGGTTCGAGCGATTCTCCTTCCTCAGTCTCCCAAGCAGC A G NUDT19 Ensembl:ENSG00000213965 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1468765117 Functional Loss SNV dbSNP153 33..33 33 - - - 26197 RMVar_ID_26197 Human_SNP_ID_663769313 A-to-I Human chr19 + 32705008 32705008 32705008 AGGCACCTGTAATCCCAGCTACTTGGGGGGCCAAGGCAGAAGAATCGGTTGAACCTGGGAGGCAG AGGCACCTGTAATCCCAGCTACTTGGGGGGCCGAGGCAGAAGAATCGGTTGAACCTGGGAGGCAG A G NUDT19 Ensembl:ENSG00000213965 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1448563936 Functional Loss SNV dbSNP153 33..33 33 - - - 26198 RMVar_ID_26198 Human_SNP_ID_663814803 A-to-I Human chr19 - 32877671 32877671 32877671 CTCCTGCCTAGGCCTCCCAAAGTGTTGGGATTATAGGTATGAGCCACCGCGCCTGGTCTGGGAAG CTCCTGCCTAGGCCTCCCAAAGTGTTGGGATTGTAGGTATGAGCCACCGCGCCTGGTCTGGGAAG T C CEP89 Ensembl:ENSG00000121289 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956560937 Functional Loss SNV dbSNP153 33..33 33 - - - 26199 RMVar_ID_26199 Human_SNP_ID_663814932 A-to-I Human chr19 - 32878223 32878223 32878223 TTGTTTGTTTTGAGACAGGGTCTCACTCTGTTACCCAGGCTGGAATGCAGTGGTGCAATCACCAC TTGTTTGTTTTGAGACAGGGTCTCACTCTGTTGCCCAGGCTGGAATGCAGTGGTGCAATCACCAC T C CEP89 Ensembl:ENSG00000121289 Protein coding exon GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1432389357 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26473914 26200 RMVar_ID_26200 Human_SNP_ID_663837477 A-to-I Human chr19 - 32970564 32970564 32970564 TAAACCCGAGAGGCAGAGGTTGCAGTGAGCCAAGATTGTGCCACTGCACTCCAGCCTGGGCGACA TAAACCCGAGAGGCAGAGGTTGCAGTGAGCCAGGATTGTGCCACTGCACTCCAGCCTGGGCGACA T C CEP89 Ensembl:ENSG00000121289 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-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 26201 RMVar_ID_26201 Human_SNP_ID_663837691 A-to-I Human chr19 - 32971575 32971575 32971575 ATAGCTCACTGCATCCTCGAACTCCTGGGCTCAAGCGATCTTCCCACCCCAGCCTCCCGAGGAGC ATAGCTCACTGCATCCTCGAACTCCTGGGCTCCAGCGATCTTCCCACCCCAGCCTCCCGAGGAGC T G CEP89 Ensembl:ENSG00000121289 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs927659307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_519147,Human_RBP_ID_13427279 Human_Splice_Rec_1989728,Human_Splice_Rec_1989730 Human_miRNA_ID_2686197 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 26202 RMVar_ID_26202 Human_SNP_ID_663866231 A-to-I Human chr19 + 33083655 33083655 33083655 TAGGTCAAGCAATCCATCTGCCTTCACCTCCCAAAGTGTTGGAATTACAGGCGTGAGCCATTGCA TAGGTCAAGCAATCCATCTGCCTTCACCTCCCGAAGTGTTGGAATTACAGGCGTGAGCCATTGCA A G GPATCH1 Ensembl:ENSG00000076650 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982852978 Functional Loss SNV dbSNP153 33..33 33 - - - 26203 RMVar_ID_26203 Human_SNP_ID_663878104 A-to-I Human chr19 + 33131167 33131167 33131167 AAATACAAAAAAATTAGCCAGGTCTGGTGAGCATACACCTGTAATCCCAGCTGTGTGGGAGGCTG AAATACAAAAAAATTAGCCAGGTCTGGTGAGCGTACACCTGTAATCCCAGCTGTGTGGGAGGCTG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs549868685 Functional Loss SNV dbSNP153 33..33 33 - - - 26204 RMVar_ID_26204 Human_SNP_ID_663888508 A-to-I Human chr19 - 33170276 33170276 33170276 CTACTCGGGAGGCTAAGGCGGGAGGATCGCCTAAGCCCGGGAGGTTCAGGCTGCAGTGAGCTGAG CTACTCGGGAGGCTAAGGCGGGAGGATCGCCTGAGCCCGGGAGGTTCAGGCTGCAGTGAGCTGAG T C HSALNG0125414 RNACentral:URS0000EA4FA0 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1056930172 Functional Loss SNV dbSNP153 33..33 33 - - - 26205 RMVar_ID_26205 Human_SNP_ID_663888526 A-to-I Human chr19 - 33170315 33170314 33170315 AATTAGCCAGGCATGATCGCGGGCACCTTGTAATCCCAGCTACTCGGGAGGCTAAGGCGGGAGGA AATTAGCCAGGCATGATCGCGGGCACCTTGTA_TCCCAGCTACTCGGGAGGCTAAGGCGGGAGGA AT A HSALNG0125414 RNACentral:URS0000EA4FA0 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1291981005 Functional Loss DEL dbSNP153 33..33 33 - - - 26206 RMVar_ID_26206 Human_SNP_ID_663888533 A-to-I Human chr19 - 33170350 33170350 33170350 CATGGGAAAACCCCGCCTCCGCTAAAAATACAAAAAATTAGCCAGGCATGATCGCGGGCACCTTG CATGGGAAAACCCCGCCTCCGCTAAAAATACAGAAAATTAGCCAGGCATGATCGCGGGCACCTTG T C HSALNG0125414 RNACentral:URS0000EA4FA0 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1293849695 Functional Loss SNV dbSNP153 33..33 33 - - - 26207 RMVar_ID_26207 Human_SNP_ID_663889796 A-to-I Human chr19 - 33175123 33175123 33175123 TCAAGCAATTCTCCTGCCTCAGCCACCCGAGTAGCTGGGATTACAGGCGTGCACCACCACATCCT TCAAGCAATTCTCCTGCCTCAGCCACCCGAGTGGCTGGGATTACAGGCGTGCACCACCACATCCT T C HSALNG0125414 RNACentral:URS0000EA4FA0 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749943099 Functional Loss SNV dbSNP153 33..33 33 - - - 26208 RMVar_ID_26208 Human_SNP_ID_663966014 A-to-I Human chr19 - 33457260 33457260 33457260 TGCCCAGCTAATTTTTTATTTTTCGTAGAGATAGAGTTTTGCCTTGTTGCCCAGGCTGGTCTAGA TGCCCAGCTAATTTTTTATTTTTCGTAGAGATGGAGTTTTGCCTTGTTGCCCAGGCTGGTCTAGA T C PEPD Ensembl:ENSG00000124299 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1366617490 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114883,RMVar_hsa_circ_194022 26209 RMVar_ID_26209 Human_SNP_ID_664141297 A-to-I Human chr19 + 34135622 34135622 34135622 AATGGCCAGACTGGGCTTGAACTCCCGACCTCAAGTGATTCACCCTCCTCGGCCTCCGTAAGTGC AATGGCCAGACTGGGCTTGAACTCCCGACCTCGAGTGATTCACCCTCCTCGGCCTCCGTAAGTGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1269975162 Functional Loss SNV dbSNP153 33..33 33 - - - 26210 RMVar_ID_26210 Human_SNP_ID_664154305 A-to-I Human chr19 + 34188150 34188150 34188150 CTCTACAAAAAATACAAAAATTAGCCAGGTGTAGTGTGTGTGCCTGTAGTTCTAGCTACTCAAGA CTCTACAAAAAATACAAAAATTAGCCAGGTGTGGTGTGTGTGCCTGTAGTTCTAGCTACTCAAGA A G LSM14A Ensembl:ENSG00000257103 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs931626566 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_194031,RMVar_hsa_circ_103512,RMVar_hsa_circ_194032 26211 RMVar_ID_26211 Human_SNP_ID_664155410 A-to-I Human chr19 + 34192513 34192513 34192513 ATGCCCAGCTAATGATTTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATTTTGTTGAGGCCGG ATGCCCAGCTAATGATTTTTTGTATTTTTAGTGGAGATGGGGTTTCACCATTTTGTTGAGGCCGG A G LSM14A Ensembl:ENSG00000257103 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1361382965 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_194031,RMVar_hsa_circ_103512,RMVar_hsa_circ_194032 26212 RMVar_ID_26212 Human_SNP_ID_664157012 A-to-I Human chr19 + 34198522 34198522 34198522 CCTGTAATCCCGGCTACTAGGGAGGCTGAGGTAGGAGAATCGCTTGAACCTGTGAGGCAGAGGTT CCTGTAATCCCGGCTACTAGGGAGGCTGAGGTGGGAGAATCGCTTGAACCTGTGAGGCAGAGGTT A G LSM14A Ensembl:ENSG00000257103 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs560144424 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3091,RMVar_hsa_circ_194031,RMVar_hsa_circ_103512,RMVar_hsa_circ_289198,RMVar_hsa_circ_194032,RMVar_hsa_circ_309294,RMVar_hsa_circ_273443,RMVar_hsa_circ_22434,RMVar_hsa_circ_21740,RMVar_hsa_circ_194040,RMVar_hsa_circ_194035,RMVar_hsa_circ_194037,RMVar_hsa_circ_194036,RMVar_hsa_circ_194033,RMVar_hsa_circ_194034,RMVar_hsa_circ_277968,RMVar_hsa_circ_295725,RMVar_hsa_circ_361145,RMVar_hsa_circ_194041 26213 RMVar_ID_26213 Human_SNP_ID_664157133 A-to-I Human chr19 + 34198944 34198944 34198944 AGGAGGCGGAGCTTGCGGTGAGCCAAGATCGTACCACTGCACTCCAGCCTGGGCGACAGAGTGAG AGGAGGCGGAGCTTGCGGTGAGCCAAGATCGTGCCACTGCACTCCAGCCTGGGCGACAGAGTGAG A G LSM14A Ensembl:ENSG00000257103 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1367406384 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3091,RMVar_hsa_circ_194031,RMVar_hsa_circ_103512,RMVar_hsa_circ_289198,RMVar_hsa_circ_194032,RMVar_hsa_circ_309294,RMVar_hsa_circ_273443,RMVar_hsa_circ_22434,RMVar_hsa_circ_21740,RMVar_hsa_circ_194040,RMVar_hsa_circ_194035,RMVar_hsa_circ_194037,RMVar_hsa_circ_194036,RMVar_hsa_circ_194033,RMVar_hsa_circ_194034,RMVar_hsa_circ_277968,RMVar_hsa_circ_295725,RMVar_hsa_circ_361145,RMVar_hsa_circ_194041 26214 RMVar_ID_26214 Human_SNP_ID_664157197 A-to-I Human chr19 + 34199168 34199168 34199168 ATTTATTTTGAGATAAGATCTGGCTCTCACCCAGGCTGGAGTGCAGTGGCACGATCCCGGCTCAT ATTTATTTTGAGATAAGATCTGGCTCTCACCCGGGCTGGAGTGCAGTGGCACGATCCCGGCTCAT A G LSM14A Ensembl:ENSG00000257103 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1052530495 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6742894,Human_RBP_ID_13429316 RMVar_hsa_circ_3091,RMVar_hsa_circ_194031,RMVar_hsa_circ_103512,RMVar_hsa_circ_289198,RMVar_hsa_circ_194032,RMVar_hsa_circ_309294,RMVar_hsa_circ_273443,RMVar_hsa_circ_22434,RMVar_hsa_circ_21740,RMVar_hsa_circ_194040,RMVar_hsa_circ_194035,RMVar_hsa_circ_194037,RMVar_hsa_circ_194036,RMVar_hsa_circ_194033,RMVar_hsa_circ_194034,RMVar_hsa_circ_277968,RMVar_hsa_circ_295725,RMVar_hsa_circ_361145,RMVar_hsa_circ_194041 26215 RMVar_ID_26215 Human_SNP_ID_664157217 A-to-I Human chr19 + 34199242 34199242 34199242 CGCCTCCCAGGCTCAAGCCATCCTCCCACCTCAACCTCCCGAGTAGCTGGGATTATAGGCATGCA CGCCTCCCAGGCTCAAGCCATCCTCCCACCTCCACCTCCCGAGTAGCTGGGATTATAGGCATGCA A C LSM14A Ensembl:ENSG00000257103 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1327065209 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3091,RMVar_hsa_circ_194031,RMVar_hsa_circ_103512,RMVar_hsa_circ_289198,RMVar_hsa_circ_194032,RMVar_hsa_circ_309294,RMVar_hsa_circ_273443,RMVar_hsa_circ_22434,RMVar_hsa_circ_21740,RMVar_hsa_circ_194040,RMVar_hsa_circ_194035,RMVar_hsa_circ_194037,RMVar_hsa_circ_194036,RMVar_hsa_circ_194033,RMVar_hsa_circ_194034,RMVar_hsa_circ_277968,RMVar_hsa_circ_295725,RMVar_hsa_circ_361145,RMVar_hsa_circ_194041 26216 RMVar_ID_26216 Human_SNP_ID_664157233 A-to-I Human chr19 + 34199270 34199270 34199270 CCTCAACCTCCCGAGTAGCTGGGATTATAGGCATGCACCACCACTCCCGGCTAGATTTTTCTTTT CCTCAACCTCCCGAGTAGCTGGGATTATAGGCGTGCACCACCACTCCCGGCTAGATTTTTCTTTT A G LSM14A Ensembl:ENSG00000257103 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1023031590 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6742896 RMVar_hsa_circ_3091,RMVar_hsa_circ_194031,RMVar_hsa_circ_103512,RMVar_hsa_circ_289198,RMVar_hsa_circ_194032,RMVar_hsa_circ_309294,RMVar_hsa_circ_273443,RMVar_hsa_circ_22434,RMVar_hsa_circ_21740,RMVar_hsa_circ_194040,RMVar_hsa_circ_194035,RMVar_hsa_circ_194037,RMVar_hsa_circ_194036,RMVar_hsa_circ_194033,RMVar_hsa_circ_194034,RMVar_hsa_circ_277968,RMVar_hsa_circ_295725,RMVar_hsa_circ_361145,RMVar_hsa_circ_194041 26217 RMVar_ID_26217 Human_SNP_ID_664157246 A-to-I Human chr19 + 34199305 34199305 34199305 CACCACCACTCCCGGCTAGATTTTTCTTTTGTATTTTTTGTGGAGACAGGGTTTCCCCATATTTT CACCACCACTCCCGGCTAGATTTTTCTTTTGTGTTTTTTGTGGAGACAGGGTTTCCCCATATTTT A G LSM14A Ensembl:ENSG00000257103 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs374622726 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6742896,Human_RBP_ID_9915144,Human_RBP_ID_23175877 RMVar_hsa_circ_3091,RMVar_hsa_circ_194031,RMVar_hsa_circ_103512,RMVar_hsa_circ_289198,RMVar_hsa_circ_194032,RMVar_hsa_circ_309294,RMVar_hsa_circ_273443,RMVar_hsa_circ_22434,RMVar_hsa_circ_21740,RMVar_hsa_circ_194040,RMVar_hsa_circ_194035,RMVar_hsa_circ_194037,RMVar_hsa_circ_194036,RMVar_hsa_circ_194033,RMVar_hsa_circ_194034,RMVar_hsa_circ_277968,RMVar_hsa_circ_295725,RMVar_hsa_circ_361145,RMVar_hsa_circ_194041 26218 RMVar_ID_26218 Human_SNP_ID_664157251 A-to-I Human chr19 + 34199331 34199331 34199331 TTTTGTATTTTTTGTGGAGACAGGGTTTCCCCATATTTTCCAGGCTGGTCTCAAACTTGTGACCT TTTTGTATTTTTTGTGGAGACAGGGTTTCCCCGTATTTTCCAGGCTGGTCTCAAACTTGTGACCT A G LSM14A Ensembl:ENSG00000257103 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs561581978 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8255960,Human_RBP_ID_13429317,Human_RBP_ID_25401394 RMVar_hsa_circ_3091,RMVar_hsa_circ_194031,RMVar_hsa_circ_103512,RMVar_hsa_circ_289198,RMVar_hsa_circ_194032,RMVar_hsa_circ_309294,RMVar_hsa_circ_273443,RMVar_hsa_circ_22434,RMVar_hsa_circ_21740,RMVar_hsa_circ_194040,RMVar_hsa_circ_194035,RMVar_hsa_circ_194037,RMVar_hsa_circ_194036,RMVar_hsa_circ_194033,RMVar_hsa_circ_194034,RMVar_hsa_circ_277968,RMVar_hsa_circ_295725,RMVar_hsa_circ_361145,RMVar_hsa_circ_194041 26219 RMVar_ID_26219 Human_SNP_ID_664157252 A-to-I Human chr19 + 34199333 34199333 34199333 TTGTATTTTTTGTGGAGACAGGGTTTCCCCATATTTTCCAGGCTGGTCTCAAACTTGTGACCTTG TTGTATTTTTTGTGGAGACAGGGTTTCCCCATGTTTTCCAGGCTGGTCTCAAACTTGTGACCTTG A G LSM14A Ensembl:ENSG00000257103 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1307183401 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8255960,Human_RBP_ID_13429317,Human_RBP_ID_25401395 RMVar_hsa_circ_3091,RMVar_hsa_circ_194031,RMVar_hsa_circ_103512,RMVar_hsa_circ_289198,RMVar_hsa_circ_194032,RMVar_hsa_circ_309294,RMVar_hsa_circ_273443,RMVar_hsa_circ_22434,RMVar_hsa_circ_21740,RMVar_hsa_circ_194040,RMVar_hsa_circ_194035,RMVar_hsa_circ_194037,RMVar_hsa_circ_194036,RMVar_hsa_circ_194033,RMVar_hsa_circ_194034,RMVar_hsa_circ_277968,RMVar_hsa_circ_295725,RMVar_hsa_circ_361145,RMVar_hsa_circ_194041 26220 RMVar_ID_26220 Human_SNP_ID_664157270 A-to-I Human chr19 + 34199405 34199405 34199405 CGCCCATCTTGGCCTCCAAAAGTGTTGGGATTACAGGTGTGAGCCACTGCACCCAGCCAGGTGTT CGCCCATCTTGGCCTCCAAAAGTGTTGGGATTGCAGGTGTGAGCCACTGCACCCAGCCAGGTGTT A G LSM14A Ensembl:ENSG00000257103 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1435908437 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23175880 RMVar_hsa_circ_3091,RMVar_hsa_circ_194031,RMVar_hsa_circ_103512,RMVar_hsa_circ_289198,RMVar_hsa_circ_194032,RMVar_hsa_circ_309294,RMVar_hsa_circ_273443,RMVar_hsa_circ_22434,RMVar_hsa_circ_21740,RMVar_hsa_circ_194040,RMVar_hsa_circ_194035,RMVar_hsa_circ_194037,RMVar_hsa_circ_194036,RMVar_hsa_circ_194033,RMVar_hsa_circ_194034,RMVar_hsa_circ_277968,RMVar_hsa_circ_295725,RMVar_hsa_circ_361145,RMVar_hsa_circ_194041 26221 RMVar_ID_26221 Human_SNP_ID_664161722 A-to-I Human chr19 + 34216529 34216529 34216529 TTACCCAGGCTGTAGTGCAGTGGTGTGATCTCAGCTCACGGCAGCCTCCGCCTCCCGGGTTCAAG TTACCCAGGCTGTAGTGCAGTGGTGTGATCTCTGCTCACGGCAGCCTCCGCCTCCCGGGTTCAAG A T LSM14A Ensembl:ENSG00000257103 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1338747902 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3091,RMVar_hsa_circ_309294,RMVar_hsa_circ_21740,RMVar_hsa_circ_194035,RMVar_hsa_circ_194033,RMVar_hsa_circ_194034,RMVar_hsa_circ_295725,RMVar_hsa_circ_194041,RMVar_hsa_circ_194044,RMVar_hsa_circ_358759,RMVar_hsa_circ_282258,RMVar_hsa_circ_194043,RMVar_hsa_circ_194047,RMVar_hsa_circ_321552,RMVar_hsa_circ_363461,RMVar_hsa_circ_341575,RMVar_hsa_circ_194048 26222 RMVar_ID_26222 Human_SNP_ID_664161734 A-to-I Human chr19 + 34216563 34216563 34216563 CTCACGGCAGCCTCCGCCTCCCGGGTTCAAGTAATTCTCCTGCCTCAGCCTCCCTAGTAGCTGGG CTCACGGCAGCCTCCGCCTCCCGGGTTCAAGTCATTCTCCTGCCTCAGCCTCCCTAGTAGCTGGG A C LSM14A Ensembl:ENSG00000257103 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1255997895 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3091,RMVar_hsa_circ_309294,RMVar_hsa_circ_21740,RMVar_hsa_circ_194035,RMVar_hsa_circ_194033,RMVar_hsa_circ_194034,RMVar_hsa_circ_295725,RMVar_hsa_circ_194041,RMVar_hsa_circ_194044,RMVar_hsa_circ_358759,RMVar_hsa_circ_282258,RMVar_hsa_circ_194043,RMVar_hsa_circ_194047,RMVar_hsa_circ_321552,RMVar_hsa_circ_363461,RMVar_hsa_circ_341575,RMVar_hsa_circ_194048 26223 RMVar_ID_26223 Human_SNP_ID_664161758 A-to-I Human chr19 + 34216694 34216694 34216694 GTTGGCCAGGCTGGCCTCAAACTCCTGACCTTATTTTCCACCCACCTCAGCCTCCCGAAGTATTG GTTGGCCAGGCTGGCCTCAAACTCCTGACCTTGTTTTCCACCCACCTCAGCCTCCCGAAGTATTG A G LSM14A Ensembl:ENSG00000257103 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1490620125 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8255961 RMVar_hsa_circ_3091,RMVar_hsa_circ_309294,RMVar_hsa_circ_21740,RMVar_hsa_circ_194035,RMVar_hsa_circ_194033,RMVar_hsa_circ_194034,RMVar_hsa_circ_295725,RMVar_hsa_circ_194041,RMVar_hsa_circ_194044,RMVar_hsa_circ_358759,RMVar_hsa_circ_282258,RMVar_hsa_circ_194043,RMVar_hsa_circ_194047,RMVar_hsa_circ_321552,RMVar_hsa_circ_363461,RMVar_hsa_circ_341575,RMVar_hsa_circ_194048 26224 RMVar_ID_26224 Human_SNP_ID_664161771 A-to-I Human chr19 + 34216723 34216723 34216723 CTTATTTTCCACCCACCTCAGCCTCCCGAAGTATTGGGATTATAGGCGTGAGCCACCGCACCCAG CTTATTTTCCACCCACCTCAGCCTCCCGAAGTGTTGGGATTATAGGCGTGAGCCACCGCACCCAG A G LSM14A Ensembl:ENSG00000257103 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1454067256 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3091,RMVar_hsa_circ_309294,RMVar_hsa_circ_21740,RMVar_hsa_circ_194035,RMVar_hsa_circ_194033,RMVar_hsa_circ_194034,RMVar_hsa_circ_295725,RMVar_hsa_circ_194041,RMVar_hsa_circ_194044,RMVar_hsa_circ_358759,RMVar_hsa_circ_282258,RMVar_hsa_circ_194043,RMVar_hsa_circ_194047,RMVar_hsa_circ_321552,RMVar_hsa_circ_363461,RMVar_hsa_circ_341575,RMVar_hsa_circ_194048 26225 RMVar_ID_26225 Human_SNP_ID_664161775 A-to-I Human chr19 + 34216732 34216732 34216732 CACCCACCTCAGCCTCCCGAAGTATTGGGATTATAGGCGTGAGCCACCGCACCCAGCCAGGCAGT CACCCACCTCAGCCTCCCGAAGTATTGGGATTGTAGGCGTGAGCCACCGCACCCAGCCAGGCAGT A G LSM14A Ensembl:ENSG00000257103 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1003962142 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3091,RMVar_hsa_circ_309294,RMVar_hsa_circ_21740,RMVar_hsa_circ_194035,RMVar_hsa_circ_194033,RMVar_hsa_circ_194034,RMVar_hsa_circ_295725,RMVar_hsa_circ_194041,RMVar_hsa_circ_194044,RMVar_hsa_circ_358759,RMVar_hsa_circ_282258,RMVar_hsa_circ_194043,RMVar_hsa_circ_194047,RMVar_hsa_circ_321552,RMVar_hsa_circ_363461,RMVar_hsa_circ_341575,RMVar_hsa_circ_194048 26226 RMVar_ID_26226 Human_SNP_ID_664161835 A-to-I Human chr19 + 34216984 34216984 34216984 ACGTTTCCTCATTAAAATTAAGCCCAGAGGCCAGGCACGGTGGCTCACACCTGTAATCTCAGCAC ACGTTTCCTCATTAAAATTAAGCCCAGAGGCCGGGCACGGTGGCTCACACCTGTAATCTCAGCAC A G LSM14A Ensembl:ENSG00000257103 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1447573711 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3091,RMVar_hsa_circ_309294,RMVar_hsa_circ_21740,RMVar_hsa_circ_194035,RMVar_hsa_circ_194033,RMVar_hsa_circ_194034,RMVar_hsa_circ_295725,RMVar_hsa_circ_194041,RMVar_hsa_circ_194044,RMVar_hsa_circ_358759,RMVar_hsa_circ_282258,RMVar_hsa_circ_194043,RMVar_hsa_circ_194047,RMVar_hsa_circ_321552,RMVar_hsa_circ_363461,RMVar_hsa_circ_341575,RMVar_hsa_circ_194048 26227 RMVar_ID_26227 Human_SNP_ID_664161881 A-to-I Human chr19 + 34217094 34217094 34217094 TCAGCCTGGCCATACGGTGAAACCCTGTCTCTACTAAAAATAGAAAAATTAGCTGGGTGTGGTGG TCAGCCTGGCCATACGGTGAAACCCTGTCTCTGCTAAAAATAGAAAAATTAGCTGGGTGTGGTGG A G LSM14A Ensembl:ENSG00000257103 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs892131337 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3091,RMVar_hsa_circ_309294,RMVar_hsa_circ_21740,RMVar_hsa_circ_194035,RMVar_hsa_circ_194033,RMVar_hsa_circ_194034,RMVar_hsa_circ_295725,RMVar_hsa_circ_194041,RMVar_hsa_circ_194044,RMVar_hsa_circ_358759,RMVar_hsa_circ_282258,RMVar_hsa_circ_194043,RMVar_hsa_circ_194047,RMVar_hsa_circ_321552,RMVar_hsa_circ_363461,RMVar_hsa_circ_341575,RMVar_hsa_circ_194048 26228 RMVar_ID_26228 Human_SNP_ID_664161891 A-to-I Human chr19 + 34217138 34217138 34217138 AAAATTAGCTGGGTGTGGTGGCACACGCCTGTAGTCCCAGCTGCTCGGGAGGCTGAGGCAGGAGA AAAATTAGCTGGGTGTGGTGGCACACGCCTGTCGTCCCAGCTGCTCGGGAGGCTGAGGCAGGAGA A C LSM14A Ensembl:ENSG00000257103 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1021951808 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3091,RMVar_hsa_circ_309294,RMVar_hsa_circ_21740,RMVar_hsa_circ_194035,RMVar_hsa_circ_194033,RMVar_hsa_circ_194034,RMVar_hsa_circ_295725,RMVar_hsa_circ_194041,RMVar_hsa_circ_194044,RMVar_hsa_circ_358759,RMVar_hsa_circ_282258,RMVar_hsa_circ_194043,RMVar_hsa_circ_194047,RMVar_hsa_circ_321552,RMVar_hsa_circ_363461,RMVar_hsa_circ_341575,RMVar_hsa_circ_194048 26229 RMVar_ID_26229 Human_SNP_ID_664162134 A-to-I Human chr19 + 34217699 34217699 34217699 ACCCAGGCTGGAGTGCAGTGGGGCACGATCTCAGCTCACTGCAACCTCCACCGCCCGGGTTCATG ACCCAGGCTGGAGTGCAGTGGGGCACGATCTCGGCTCACTGCAACCTCCACCGCCCGGGTTCATG A G LSM14A Ensembl:ENSG00000257103 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1461480434 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13429922 RMVar_hsa_circ_3091,RMVar_hsa_circ_309294,RMVar_hsa_circ_21740,RMVar_hsa_circ_194035,RMVar_hsa_circ_194033,RMVar_hsa_circ_194034,RMVar_hsa_circ_295725,RMVar_hsa_circ_194041,RMVar_hsa_circ_194044,RMVar_hsa_circ_358759,RMVar_hsa_circ_282258,RMVar_hsa_circ_194043,RMVar_hsa_circ_194047,RMVar_hsa_circ_321552,RMVar_hsa_circ_363461,RMVar_hsa_circ_341575,RMVar_hsa_circ_194048 26230 RMVar_ID_26230 Human_SNP_ID_664162135 A-to-I Human chr19 + 34217699 34217699 34217699 ACCCAGGCTGGAGTGCAGTGGGGCACGATCTCAGCTCACTGCAACCTCCACCGCCCGGGTTCATG ACCCAGGCTGGAGTGCAGTGGGGCACGATCTCTGCTCACTGCAACCTCCACCGCCCGGGTTCATG A T LSM14A Ensembl:ENSG00000257103 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1461480434 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13429922 RMVar_hsa_circ_3091,RMVar_hsa_circ_309294,RMVar_hsa_circ_21740,RMVar_hsa_circ_194035,RMVar_hsa_circ_194033,RMVar_hsa_circ_194034,RMVar_hsa_circ_295725,RMVar_hsa_circ_194041,RMVar_hsa_circ_194044,RMVar_hsa_circ_358759,RMVar_hsa_circ_282258,RMVar_hsa_circ_194043,RMVar_hsa_circ_194047,RMVar_hsa_circ_321552,RMVar_hsa_circ_363461,RMVar_hsa_circ_341575,RMVar_hsa_circ_194048 26231 RMVar_ID_26231 Human_SNP_ID_664163795 A-to-I Human chr19 + 34224201 34224201 34224201 AAACATAAAAAAAATTAGCCGGGCGTGGTGGCACACACCTGTAATCCCAGCTACTCGGGAGGCTG AAACATAAAAAAAATTAGCCGGGCGTGGTGGCGCACACCTGTAATCCCAGCTACTCGGGAGGCTG A G LSM14A Ensembl:ENSG00000257103 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1386317300 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_141467 RMVar_hsa_circ_194033 26232 RMVar_ID_26232 Human_SNP_ID_664163797 A-to-I Human chr19 + 34224205 34224205 34224205 ATAAAAAAAATTAGCCGGGCGTGGTGGCACACACCTGTAATCCCAGCTACTCGGGAGGCTGAGGC ATAAAAAAAATTAGCCGGGCGTGGTGGCACACCCCTGTAATCCCAGCTACTCGGGAGGCTGAGGC A C LSM14A Ensembl:ENSG00000257103 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1265233012 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_141467 RMVar_hsa_circ_194033 26233 RMVar_ID_26233 Human_SNP_ID_664164181 A-to-I Human chr19 + 34225968 34225968 34225968 CCTGTAGTCCCAGCTACTCAGGAGGCTAAGGCAGGAGGATCAGTTGAACCTGGGAGGTCAAGGCT CCTGTAGTCCCAGCTACTCAGGAGGCTAAGGCCGGAGGATCAGTTGAACCTGGGAGGTCAAGGCT A C LSM14A Ensembl:ENSG00000257103 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs763196256 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13430240 RMVar_hsa_circ_194033 26234 RMVar_ID_26234 Human_SNP_ID_664173107 A-to-I Human chr19 + 34258675 34258675 34258675 AGCCGGACATGGCGATGGGCGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGTAGGAGAATGGTG AGCCGGACATGGCGATGGGCGCCTGTAGTCCCGGCTACTCAGGAGGCTGAGGTAGGAGAATGGTG A G KIAA0355 Ensembl:ENSG00000166398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1346605767 Functional Loss SNV dbSNP153 33..33 33 - - - 26235 RMVar_ID_26235 Human_SNP_ID_664174479 A-to-I Human chr19 + 34263721 34263721 34263721 GTTGGCCAGGTTGGTCTCGAACTCCTGACCTCAAGTGATCCATCCACCTCGGCCTCCCAAAGTGC GTTGGCCAGGTTGGTCTCGAACTCCTGACCTCGAGTGATCCATCCACCTCGGCCTCCCAAAGTGC A G KIAA0355 Ensembl:ENSG00000166398 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1389556710 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21892682 26236 RMVar_ID_26236 Human_SNP_ID_664184438 A-to-I Human chr19 + 34302522 34302522 34302522 CACCATCTTGGCCAGGCCGGTCTCGAACTCCTAACCTCAAGTGATCCACCTGCCTCAGCGTCCCA CACCATCTTGGCCAGGCCGGTCTCGAACTCCTGACCTCAAGTGATCCACCTGCCTCAGCGTCCCA A G KIAA0355 Ensembl:ENSG00000166398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1478397893 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_366010 26237 RMVar_ID_26237 Human_SNP_ID_664195772 A-to-I Human chr19 + 34347441 34347441 34347441 TAGAGATGAGGTTTTGCCGTGTTGGCCAGGCTAGTCTCGAACTTCTGGGCTCAAGCGATCTGCCC TAGAGATGAGGTTTTGCCGTGTTGGCCAGGCTGGTCTCGAACTTCTGGGCTCAAGCGATCTGCCC A G KIAA0355 Ensembl:ENSG00000166398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1182412451 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10129,RMVar_hsa_circ_194063,RMVar_hsa_circ_116805,RMVar_hsa_circ_267226 26238 RMVar_ID_26238 Human_SNP_ID_664196407 A-to-I Human chr19 + 34349974 34349974 34349974 CCAGCTACTCGGGAGGCTGAGGTGGGAGGATCACTTGAGCCTGGGAAGTTGAGGCTACAGTGAGC CCAGCTACTCGGGAGGCTGAGGTGGGAGGATCCCTTGAGCCTGGGAAGTTGAGGCTACAGTGAGC A C KIAA0355 Ensembl:ENSG00000166398 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1485854835 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35828,RMVar_hsa_circ_112029,RMVar_hsa_circ_194066,RMVar_hsa_circ_194067 26239 RMVar_ID_26239 Human_SNP_ID_664201911 A-to-I Human chr19 + 34369113 34369111 34369113 CTCTCTCGCCCAGAGTGGACTGCAGTCGTGCTATCTCAGCTCACTGCAACTTCCGCCTCCTGGAT CTCTCTCGCCCAGAGTGGACTGCAGTCGTGC__TCTCAGCTCACTGCAACTTCCGCCTCCTGGAT CTA C GPI Ensembl:ENSG00000105220 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1469880153 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_25402338 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_98226,RMVar_hsa_circ_78645,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 26240 RMVar_ID_26240 Human_SNP_ID_664201939 A-to-I Human chr19 + 34369232 34369232 34369232 CACCCTGCTCAGCTAATTTTTGTATTTTTAGTAGAGACGGGATTTCACCATGTTGGCCAGGCTGG CACCCTGCTCAGCTAATTTTTGTATTTTTAGTGGAGACGGGATTTCACCATGTTGGCCAGGCTGG A G GPI Ensembl:ENSG00000105220 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1484562815 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_194082,RMVar_hsa_circ_194083 26241 RMVar_ID_26241 Human_SNP_ID_664201957 A-to-I Human chr19 + 34369283 34369283 34369283 GTTGGCCAGGCTGGTCTCAAACCCCTGACCTCAGGTGATCTGCCTGCCTCACCTGGGATTACAGG GTTGGCCAGGCTGGTCTCAAACCCCTGACCTCGGGTGATCTGCCTGCCTCACCTGGGATTACAGG A G GPI Ensembl:ENSG00000105220 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910291725 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_194082,RMVar_hsa_circ_194083 26242 RMVar_ID_26242 Human_SNP_ID_664202021 A-to-I Human chr19 + 34369496 34369496 34369496 TGAGAGGCCGGGGTGGGTGGATCACTTGAGGTAAGGAGTTCGAGACCAGCCTGGCCATCATGGTG TGAGAGGCCGGGGTGGGTGGATCACTTGAGGTCAGGAGTTCGAGACCAGCCTGGCCATCATGGTG A C GPI Ensembl:ENSG00000105220 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1239887488 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_194082,RMVar_hsa_circ_194083 26243 RMVar_ID_26243 Human_SNP_ID_664202029 A-to-I Human chr19 + 34369529 34369529 34369529 AGGAGTTCGAGACCAGCCTGGCCATCATGGTGAAACCCCATCTCCACTAAAAATACAAAAATTAG AGGAGTTCGAGACCAGCCTGGCCATCATGGTGCAACCCCATCTCCACTAAAAATACAAAAATTAG A C GPI Ensembl:ENSG00000105220 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs555687325 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_194082,RMVar_hsa_circ_194083 26244 RMVar_ID_26244 Human_SNP_ID_664202032 A-to-I Human chr19 + 34369536 34369536 34369536 CGAGACCAGCCTGGCCATCATGGTGAAACCCCATCTCCACTAAAAATACAAAAATTAGCCAGTTT CGAGACCAGCCTGGCCATCATGGTGAAACCCCGTCTCCACTAAAAATACAAAAATTAGCCAGTTT A G GPI Ensembl:ENSG00000105220 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1379605274 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_194082,RMVar_hsa_circ_194083 26245 RMVar_ID_26245 Human_SNP_ID_664202741 A-to-I Human chr19 + 34372205 34372205 34372205 CACCCACCTTGGCCTCCCAGAGTCCTGGGATTACAGGCATGAGCCACCACACCCAGCCAAGACTT CACCCACCTTGGCCTCCCAGAGTCCTGGGATTGCAGGCATGAGCCACCACACCCAGCCAAGACTT A G GPI Ensembl:ENSG00000105220 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005516769 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_194082,RMVar_hsa_circ_194083 26246 RMVar_ID_26246 Human_SNP_ID_664202815 A-to-I Human chr19 + 34372519 34372519 34372519 TAAAAATTAGCCAGCTGTGGTGGTGTGTACCTATAGTCCTGGCTGCTTAGGAGGCTGAGGCGGGA TAAAAATTAGCCAGCTGTGGTGGTGTGTACCTGTAGTCCTGGCTGCTTAGGAGGCTGAGGCGGGA A G GPI Ensembl:ENSG00000105220 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1249228241 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13431574,Human_RBP_ID_17567661,Human_RBP_ID_25444190 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_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_194082,RMVar_hsa_circ_194083 26247 RMVar_ID_26247 Human_SNP_ID_664202960 A-to-I Human chr19 + 34373125 34373125 34373125 AAATAATTTATAGTCTGGGTGCTGTGGCTCACACCTGTAGTCCTAGCACTTTGGGAGGCCGAGGT AAATAATTTATAGTCTGGGTGCTGTGGCTCACGCCTGTAGTCCTAGCACTTTGGGAGGCCGAGGT A G GPI Ensembl:ENSG00000105220 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1162960912 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17567664 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_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_194082,RMVar_hsa_circ_194083 26248 RMVar_ID_26248 Human_SNP_ID_664202991 A-to-I Human chr19 + 34373266 34373266 34373266 ACAAAATTAGCCAGGAGTAGTGGCAGGCGCCCATAATTCCAGCTACTCAGGAGACTGAGGCAGCA ACAAAATTAGCCAGGAGTAGTGGCAGGCGCCCCTAATTCCAGCTACTCAGGAGACTGAGGCAGCA A C GPI Ensembl:ENSG00000105220 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1000311793 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_194082,RMVar_hsa_circ_194083 26249 RMVar_ID_26249 Human_SNP_ID_664202992 A-to-I Human chr19 + 34373266 34373266 34373266 ACAAAATTAGCCAGGAGTAGTGGCAGGCGCCCATAATTCCAGCTACTCAGGAGACTGAGGCAGCA ACAAAATTAGCCAGGAGTAGTGGCAGGCGCCCGTAATTCCAGCTACTCAGGAGACTGAGGCAGCA A G GPI Ensembl:ENSG00000105220 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1000311793 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_194082,RMVar_hsa_circ_194083 26250 RMVar_ID_26250 Human_SNP_ID_664202996 A-to-I Human chr19 + 34373282 34373282 34373282 GTAGTGGCAGGCGCCCATAATTCCAGCTACTCAGGAGACTGAGGCAGCAGTATCATTTGAACCCA GTAGTGGCAGGCGCCCATAATTCCAGCTACTCGGGAGACTGAGGCAGCAGTATCATTTGAACCCA A G GPI Ensembl:ENSG00000105220 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1158684543 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_194082,RMVar_hsa_circ_194083 26251 RMVar_ID_26251 Human_SNP_ID_664203472 A-to-I Human chr19 + 34375191 34375191 34375191 TTAAGACGGAGTCTTGCTCTGTCGCCCAGGCTAGAGTGCAATGGCGTGATCTCCACTCACTGCAA TTAAGACGGAGTCTTGCTCTGTCGCCCAGGCTGGAGTGCAATGGCGTGATCTCCACTCACTGCAA A G GPI Ensembl:ENSG00000105220 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs568378814 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_194082,RMVar_hsa_circ_194083 26252 RMVar_ID_26252 Human_SNP_ID_664203515 A-to-I Human chr19 + 34375350 34375350 34375350 TTTTTTTTTTTTAGCAGAGACGGGGTTTCACCATGTTGACTAGGCTGGTCTCGAACTCCTGACCT TTTTTTTTTTTTAGCAGAGACGGGGTTTCACCGTGTTGACTAGGCTGGTCTCGAACTCCTGACCT A G GPI Ensembl:ENSG00000105220 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1042184514 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13431638,Human_RBP_ID_17568029 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_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_194082,RMVar_hsa_circ_194083 26253 RMVar_ID_26253 Human_SNP_ID_664203999 A-to-I Human chr19 + 34377234 34377234 34377234 TGAGGCAGGAGAATGACGTGAACCTGGGAGGCAGAGATTGCAGGGAGCCGAGATCATGCCACTGC TGAGGCAGGAGAATGACGTGAACCTGGGAGGCGGAGATTGCAGGGAGCCGAGATCATGCCACTGC A G GPI Ensembl:ENSG00000105220 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1162431324 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_194082,RMVar_hsa_circ_194083 26254 RMVar_ID_26254 Human_SNP_ID_664204314 A-to-I Human chr19 + 34377822 34377822 34377822 TCTGGTATGTCTCCAACATTGATGGAACTCACATTGCCAAAACCCTGGCCCAGCTGAACCCCGAG TCTGGTATGTCTCCAACATTGATGGAACTCACGTTGCCAAAACCCTGGCCCAGCTGAACCCCGAG A G GPI Ensembl:ENSG00000105220 Protein coding CDS GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs367675230 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_4566118,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_18728327,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 26255 RMVar_ID_26255 Human_SNP_ID_664206365 A-to-I Human chr19 + 34385374 34385374 34385374 TTTGTCTCAAACAAAAAACAAAAAAAAAAAAAAAAGAAAAAAGATGGGTGGGTAGAAGTTCTTCT TTTGTCTCAAACAAAAAACAAAAAAAAAAAAAGAAGAAAAAAGATGGGTGGGTAGAAGTTCTTCT A G GPI Ensembl:ENSG00000105220 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs915912099 Functional Loss SNV dbSNP153 33..33 33 - - - 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 26256 RMVar_ID_26256 Human_SNP_ID_664207997 A-to-I Human chr19 - 34391579 34391579 34391579 ACCAGGGACACATCCTACCTGCTCAGACATGGACAGACCCGGATTCTCATACCAGGGCCAGATCC ACCAGGGACACATCCTACCTGCTCAGACATGGTCAGACCCGGATTCTCATACCAGGGCCAGATCC T A 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 GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs796266238 Functional Loss SNV dbSNP153 33..33 33 - - - 26257 RMVar_ID_26257 Human_SNP_ID_664207998 A-to-I Human chr19 - 34391579 34391579 34391579 ACCAGGGACACATCCTACCTGCTCAGACATGGACAGACCCGGATTCTCATACCAGGGCCAGATCC ACCAGGGACACATCCTACCTGCTCAGACATGGGCAGACCCGGATTCTCATACCAGGGCCAGATCC 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 GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs796266238 Functional Loss SNV dbSNP153 33..33 33 - - - 26258 RMVar_ID_26258 Human_SNP_ID_664208302 A-to-I Human chr19 + 34392045 34392045 34392045 AAGGATCTGGGTCTTTCAATGTCTGAGAAGGTAGGATCTGGTACAGGTGTGAGGATCTGGGTCTG AAGGATCTGGGTCTTTCAATGTCTGAGAAGGTGGGATCTGGTACAGGTGTGAGGATCTGGGTCTG A G GPI Ensembl:ENSG00000105220 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1426433207 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7655,Human_RBP_ID_53173,Human_RBP_ID_823621,Human_RBP_ID_2563512,Human_RBP_ID_4519464,Human_RBP_ID_5238760,Human_RBP_ID_8100579,Human_RBP_ID_8832305,Human_RBP_ID_9086636,Human_RBP_ID_9915961,Human_RBP_ID_13432293,Human_RBP_ID_17131298,Human_RBP_ID_22447655,Human_RBP_ID_22502327,Human_RBP_ID_22977466,Human_RBP_ID_23279037,Human_RBP_ID_23792777,Human_RBP_ID_24374527,Human_RBP_ID_26783750,Human_RBP_ID_27677268,Human_RBP_ID_27839504 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 26259 RMVar_ID_26259 Human_SNP_ID_664208678 A-to-I Human chr19 + 34392583 34392580 34392583 TGGCCCTGGTATGAGGATCTGGGTCTGTCAGTATCTGAGGAGGTAGGATCTCATACAGGTATGAG TGGCCCTGGTATGAGGATCTGGGTCTGTCCATGTCTGAGGAGGTAGGATCTCATACAGGTATGAG AGTA CATG GPI Ensembl:ENSG00000105220 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1568346319 Functional Loss MNV dbSNP153 30..33 33 - - - Human_RBP_ID_7657,Human_RBP_ID_823624,Human_RBP_ID_1293396,Human_RBP_ID_5239348,Human_RBP_ID_8102937,Human_RBP_ID_9086656,Human_RBP_ID_9915975,Human_RBP_ID_13432347,Human_RBP_ID_17131315,Human_RBP_ID_21978568,Human_RBP_ID_22591717,Human_RBP_ID_22719200,Human_RBP_ID_22969955,Human_RBP_ID_23279218,Human_RBP_ID_24374532,Human_RBP_ID_26783752,Human_RBP_ID_27839909 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 26260 RMVar_ID_26260 Human_SNP_ID_664208681 A-to-I Human chr19 + 34392583 34392583 34392583 TGGCCCTGGTATGAGGATCTGGGTCTGTCAGTATCTGAGGAGGTAGGATCTCATACAGGTATGAG TGGCCCTGGTATGAGGATCTGGGTCTGTCAGTGTCTGAGGAGGTAGGATCTCATACAGGTATGAG A G GPI Ensembl:ENSG00000105220 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs796272912 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7657,Human_RBP_ID_823624,Human_RBP_ID_1293396,Human_RBP_ID_5239348,Human_RBP_ID_8102937,Human_RBP_ID_9086656,Human_RBP_ID_9915975,Human_RBP_ID_13432347,Human_RBP_ID_17131315,Human_RBP_ID_21978568,Human_RBP_ID_22591717,Human_RBP_ID_22719200,Human_RBP_ID_22969955,Human_RBP_ID_23279218,Human_RBP_ID_24374532,Human_RBP_ID_26783752,Human_RBP_ID_27839909 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 26261 RMVar_ID_26261 Human_SNP_ID_664208695 A-to-I Human chr19 + 34392603 34392603 34392603 GGGTCTGTCAGTATCTGAGGAGGTAGGATCTCATACAGGTATGAGGATCTGGGTTTTTCAATGTC GGGTCTGTCAGTATCTGAGGAGGTAGGATCTCGTACAGGTATGAGGATCTGGGTTTTTCAATGTC A G GPI Ensembl:ENSG00000105220 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs796133578 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1293396,Human_RBP_ID_13432347,Human_RBP_ID_17131315,Human_RBP_ID_18728392,Human_RBP_ID_22591717,Human_RBP_ID_27677279 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 26262 RMVar_ID_26262 Human_SNP_ID_664211136 A-to-I Human chr19 + 34401574 34401574 34401574 CCAGACTAGACTGGTCTTGAATTCCAGGGCTCAAGAGATCTCCCACCTCAGCCTCCCACAGTGCT CCAGACTAGACTGGTCTTGAATTCCAGGGCTCGAGAGATCTCCCACCTCAGCCTCCCACAGTGCT A G AC092073.1,GPI Ensembl:ENSG00000266953,Ensembl:ENSG00000105220 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs542064772 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1884067,Human_RBP_ID_4519594,Human_RBP_ID_6744571,Human_RBP_ID_8483816,Human_RBP_ID_9086684,Human_RBP_ID_13432620,Human_RBP_ID_17267958,Human_RBP_ID_18303549,Human_RBP_ID_23176134,Human_RBP_ID_26467290 Human_miRNA_ID_2866576,Human_miRNA_ID_2866577 RMVar_hsa_circ_79762,RMVar_hsa_circ_77174,RMVar_hsa_circ_194078,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_94933,RMVar_hsa_circ_104537,RMVar_hsa_circ_194102,RMVar_hsa_circ_194103,RMVar_hsa_circ_194104 26263 RMVar_ID_26263 Human_SNP_ID_664211138 A-to-I Human chr19 + 34401586 34401586 34401586 GGTCTTGAATTCCAGGGCTCAAGAGATCTCCCACCTCAGCCTCCCACAGTGCTGGGATTACAGGC GGTCTTGAATTCCAGGGCTCAAGAGATCTCCCCCCTCAGCCTCCCACAGTGCTGGGATTACAGGC A C AC092073.1,GPI Ensembl:ENSG00000266953,Ensembl:ENSG00000105220 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1011417284 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6744571,Human_RBP_ID_13432620,Human_RBP_ID_17267958,Human_RBP_ID_18303549,Human_RBP_ID_26467290 Human_miRNA_ID_2716328,Human_miRNA_ID_2716329,Human_miRNA_ID_3052313,Human_miRNA_ID_3052314 RMVar_hsa_circ_79762,RMVar_hsa_circ_77174,RMVar_hsa_circ_194078,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_94933,RMVar_hsa_circ_104537,RMVar_hsa_circ_194102,RMVar_hsa_circ_194103,RMVar_hsa_circ_194104 26264 RMVar_ID_26264 Human_SNP_ID_664219061 A-to-I Human chr19 + 34429960 34429960 34429960 TTGAGACAGGGTCTGGCCCTGTCACCCTGGCTAGAGTGCAGTGGCCCGATCTCGGCTCACTGCAA TTGAGACAGGGTCTGGCCCTGTCACCCTGGCTGGAGTGCAGTGGCCCGATCTCGGCTCACTGCAA A G UBA2 Ensembl:ENSG00000126261 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1293519801 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93128,RMVar_hsa_circ_103646,RMVar_hsa_circ_194109,RMVar_hsa_circ_194110 26265 RMVar_ID_26265 Human_SNP_ID_664220087 A-to-I Human chr19 + 34433683 34433683 34433683 TGAAAAGCTCTCAAAAAGTGTGACTGTGGCTCAGCACAGTGGCTCACGCCTGTAATCCCAGCACT TGAAAAGCTCTCAAAAAGTGTGACTGTGGCTCCGCACAGTGGCTCACGCCTGTAATCCCAGCACT A C UBA2 Ensembl:ENSG00000126261 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs8109261 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2613,GWAS_ID_2614,GWAS_ID_2615,GWAS_ID_2616,GWAS_ID_2617,GWAS_ID_2618,GWAS_ID_2619,GWAS_ID_2620,GWAS_ID_2621,GWAS_ID_2622,GWAS_ID_2623,GWAS_ID_2624 RMVar_hsa_circ_93128,RMVar_hsa_circ_54140,RMVar_hsa_circ_125569,RMVar_hsa_circ_194114,RMVar_hsa_circ_279072,RMVar_hsa_circ_353894,RMVar_hsa_circ_69805,RMVar_hsa_circ_194110,RMVar_hsa_circ_363447,RMVar_hsa_circ_291250,RMVar_hsa_circ_312685,RMVar_hsa_circ_276563,RMVar_hsa_circ_276657,RMVar_hsa_circ_275866,RMVar_hsa_circ_21381,RMVar_hsa_circ_194115,RMVar_hsa_circ_285792,RMVar_hsa_circ_310937,RMVar_hsa_circ_194112,RMVar_hsa_circ_194113,RMVar_hsa_circ_194111,RMVar_hsa_circ_356926,RMVar_hsa_circ_290880,RMVar_hsa_circ_288581,RMVar_hsa_circ_281045,RMVar_hsa_circ_285276,RMVar_hsa_circ_273262,RMVar_hsa_circ_194121,RMVar_hsa_circ_194125,RMVar_hsa_circ_119372,RMVar_hsa_circ_194126,RMVar_hsa_circ_194123,RMVar_hsa_circ_194124,RMVar_hsa_circ_194122,RMVar_hsa_circ_300968,RMVar_hsa_circ_194119,RMVar_hsa_circ_194120,RMVar_hsa_circ_313831,RMVar_hsa_circ_346878,RMVar_hsa_circ_368008,RMVar_hsa_circ_315612,RMVar_hsa_circ_301892,RMVar_hsa_circ_270348,RMVar_hsa_circ_288271,RMVar_hsa_circ_104307,RMVar_hsa_circ_194130,RMVar_hsa_circ_194132,RMVar_hsa_circ_194133,RMVar_hsa_circ_194131,RMVar_hsa_circ_194129 26266 RMVar_ID_26266 Human_SNP_ID_664220088 A-to-I Human chr19 + 34433683 34433683 34433683 TGAAAAGCTCTCAAAAAGTGTGACTGTGGCTCAGCACAGTGGCTCACGCCTGTAATCCCAGCACT TGAAAAGCTCTCAAAAAGTGTGACTGTGGCTCGGCACAGTGGCTCACGCCTGTAATCCCAGCACT A G UBA2 Ensembl:ENSG00000126261 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs8109261 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2613,GWAS_ID_2614,GWAS_ID_2615,GWAS_ID_2616,GWAS_ID_2617,GWAS_ID_2618,GWAS_ID_2619,GWAS_ID_2620,GWAS_ID_2621,GWAS_ID_2622,GWAS_ID_2623,GWAS_ID_2624 RMVar_hsa_circ_93128,RMVar_hsa_circ_54140,RMVar_hsa_circ_125569,RMVar_hsa_circ_194114,RMVar_hsa_circ_279072,RMVar_hsa_circ_353894,RMVar_hsa_circ_69805,RMVar_hsa_circ_194110,RMVar_hsa_circ_363447,RMVar_hsa_circ_291250,RMVar_hsa_circ_312685,RMVar_hsa_circ_276563,RMVar_hsa_circ_276657,RMVar_hsa_circ_275866,RMVar_hsa_circ_21381,RMVar_hsa_circ_194115,RMVar_hsa_circ_285792,RMVar_hsa_circ_310937,RMVar_hsa_circ_194112,RMVar_hsa_circ_194113,RMVar_hsa_circ_194111,RMVar_hsa_circ_356926,RMVar_hsa_circ_290880,RMVar_hsa_circ_288581,RMVar_hsa_circ_281045,RMVar_hsa_circ_285276,RMVar_hsa_circ_273262,RMVar_hsa_circ_194121,RMVar_hsa_circ_194125,RMVar_hsa_circ_119372,RMVar_hsa_circ_194126,RMVar_hsa_circ_194123,RMVar_hsa_circ_194124,RMVar_hsa_circ_194122,RMVar_hsa_circ_300968,RMVar_hsa_circ_194119,RMVar_hsa_circ_194120,RMVar_hsa_circ_313831,RMVar_hsa_circ_346878,RMVar_hsa_circ_368008,RMVar_hsa_circ_315612,RMVar_hsa_circ_301892,RMVar_hsa_circ_270348,RMVar_hsa_circ_288271,RMVar_hsa_circ_104307,RMVar_hsa_circ_194130,RMVar_hsa_circ_194132,RMVar_hsa_circ_194133,RMVar_hsa_circ_194131,RMVar_hsa_circ_194129 26267 RMVar_ID_26267 Human_SNP_ID_664220089 A-to-I Human chr19 + 34433683 34433683 34433683 TGAAAAGCTCTCAAAAAGTGTGACTGTGGCTCAGCACAGTGGCTCACGCCTGTAATCCCAGCACT TGAAAAGCTCTCAAAAAGTGTGACTGTGGCTCTGCACAGTGGCTCACGCCTGTAATCCCAGCACT A T UBA2 Ensembl:ENSG00000126261 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs8109261 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2613,GWAS_ID_2614,GWAS_ID_2615,GWAS_ID_2616,GWAS_ID_2617,GWAS_ID_2618,GWAS_ID_2619,GWAS_ID_2620,GWAS_ID_2621,GWAS_ID_2622,GWAS_ID_2623,GWAS_ID_2624 RMVar_hsa_circ_93128,RMVar_hsa_circ_54140,RMVar_hsa_circ_125569,RMVar_hsa_circ_194114,RMVar_hsa_circ_279072,RMVar_hsa_circ_353894,RMVar_hsa_circ_69805,RMVar_hsa_circ_194110,RMVar_hsa_circ_363447,RMVar_hsa_circ_291250,RMVar_hsa_circ_312685,RMVar_hsa_circ_276563,RMVar_hsa_circ_276657,RMVar_hsa_circ_275866,RMVar_hsa_circ_21381,RMVar_hsa_circ_194115,RMVar_hsa_circ_285792,RMVar_hsa_circ_310937,RMVar_hsa_circ_194112,RMVar_hsa_circ_194113,RMVar_hsa_circ_194111,RMVar_hsa_circ_356926,RMVar_hsa_circ_290880,RMVar_hsa_circ_288581,RMVar_hsa_circ_281045,RMVar_hsa_circ_285276,RMVar_hsa_circ_273262,RMVar_hsa_circ_194121,RMVar_hsa_circ_194125,RMVar_hsa_circ_119372,RMVar_hsa_circ_194126,RMVar_hsa_circ_194123,RMVar_hsa_circ_194124,RMVar_hsa_circ_194122,RMVar_hsa_circ_300968,RMVar_hsa_circ_194119,RMVar_hsa_circ_194120,RMVar_hsa_circ_313831,RMVar_hsa_circ_346878,RMVar_hsa_circ_368008,RMVar_hsa_circ_315612,RMVar_hsa_circ_301892,RMVar_hsa_circ_270348,RMVar_hsa_circ_288271,RMVar_hsa_circ_104307,RMVar_hsa_circ_194130,RMVar_hsa_circ_194132,RMVar_hsa_circ_194133,RMVar_hsa_circ_194131,RMVar_hsa_circ_194129 26268 RMVar_ID_26268 Human_SNP_ID_664220094 A-to-I Human chr19 + 34433719 34433719 34433719 CAGTGGCTCACGCCTGTAATCCCAGCACTTTGAGAGACCAAGGCAGGAGGATCACTTGAGGTCAG CAGTGGCTCACGCCTGTAATCCCAGCACTTTGCGAGACCAAGGCAGGAGGATCACTTGAGGTCAG A C UBA2 Ensembl:ENSG00000126261 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs192374884 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93128,RMVar_hsa_circ_54140,RMVar_hsa_circ_125569,RMVar_hsa_circ_194114,RMVar_hsa_circ_279072,RMVar_hsa_circ_353894,RMVar_hsa_circ_69805,RMVar_hsa_circ_194110,RMVar_hsa_circ_363447,RMVar_hsa_circ_291250,RMVar_hsa_circ_312685,RMVar_hsa_circ_276563,RMVar_hsa_circ_276657,RMVar_hsa_circ_275866,RMVar_hsa_circ_21381,RMVar_hsa_circ_194115,RMVar_hsa_circ_285792,RMVar_hsa_circ_310937,RMVar_hsa_circ_194112,RMVar_hsa_circ_194113,RMVar_hsa_circ_194111,RMVar_hsa_circ_356926,RMVar_hsa_circ_290880,RMVar_hsa_circ_288581,RMVar_hsa_circ_281045,RMVar_hsa_circ_285276,RMVar_hsa_circ_273262,RMVar_hsa_circ_194121,RMVar_hsa_circ_194125,RMVar_hsa_circ_119372,RMVar_hsa_circ_194126,RMVar_hsa_circ_194123,RMVar_hsa_circ_194124,RMVar_hsa_circ_194122,RMVar_hsa_circ_300968,RMVar_hsa_circ_194119,RMVar_hsa_circ_194120,RMVar_hsa_circ_313831,RMVar_hsa_circ_346878,RMVar_hsa_circ_368008,RMVar_hsa_circ_315612,RMVar_hsa_circ_301892,RMVar_hsa_circ_270348,RMVar_hsa_circ_288271,RMVar_hsa_circ_104307,RMVar_hsa_circ_194130,RMVar_hsa_circ_194132,RMVar_hsa_circ_194133,RMVar_hsa_circ_194131,RMVar_hsa_circ_194129 26269 RMVar_ID_26269 Human_SNP_ID_664220096 A-to-I Human chr19 + 34433726 34433726 34433726 TCACGCCTGTAATCCCAGCACTTTGAGAGACCAAGGCAGGAGGATCACTTGAGGTCAGGAGTTCG TCACGCCTGTAATCCCAGCACTTTGAGAGACCGAGGCAGGAGGATCACTTGAGGTCAGGAGTTCG A G UBA2 Ensembl:ENSG00000126261 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs952646110 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93128,RMVar_hsa_circ_54140,RMVar_hsa_circ_125569,RMVar_hsa_circ_194114,RMVar_hsa_circ_279072,RMVar_hsa_circ_353894,RMVar_hsa_circ_69805,RMVar_hsa_circ_194110,RMVar_hsa_circ_363447,RMVar_hsa_circ_291250,RMVar_hsa_circ_312685,RMVar_hsa_circ_276563,RMVar_hsa_circ_276657,RMVar_hsa_circ_275866,RMVar_hsa_circ_21381,RMVar_hsa_circ_194115,RMVar_hsa_circ_285792,RMVar_hsa_circ_310937,RMVar_hsa_circ_194112,RMVar_hsa_circ_194113,RMVar_hsa_circ_194111,RMVar_hsa_circ_356926,RMVar_hsa_circ_290880,RMVar_hsa_circ_288581,RMVar_hsa_circ_281045,RMVar_hsa_circ_285276,RMVar_hsa_circ_273262,RMVar_hsa_circ_194121,RMVar_hsa_circ_194125,RMVar_hsa_circ_119372,RMVar_hsa_circ_194126,RMVar_hsa_circ_194123,RMVar_hsa_circ_194124,RMVar_hsa_circ_194122,RMVar_hsa_circ_300968,RMVar_hsa_circ_194119,RMVar_hsa_circ_194120,RMVar_hsa_circ_313831,RMVar_hsa_circ_346878,RMVar_hsa_circ_368008,RMVar_hsa_circ_315612,RMVar_hsa_circ_301892,RMVar_hsa_circ_270348,RMVar_hsa_circ_288271,RMVar_hsa_circ_104307,RMVar_hsa_circ_194130,RMVar_hsa_circ_194132,RMVar_hsa_circ_194133,RMVar_hsa_circ_194131,RMVar_hsa_circ_194129 26270 RMVar_ID_26270 Human_SNP_ID_664220098 A-to-I Human chr19 + 34433731 34433731 34433731 CCTGTAATCCCAGCACTTTGAGAGACCAAGGCAGGAGGATCACTTGAGGTCAGGAGTTCGAGACC CCTGTAATCCCAGCACTTTGAGAGACCAAGGCTGGAGGATCACTTGAGGTCAGGAGTTCGAGACC A T UBA2 Ensembl:ENSG00000126261 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1478935166 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93128,RMVar_hsa_circ_54140,RMVar_hsa_circ_125569,RMVar_hsa_circ_194114,RMVar_hsa_circ_279072,RMVar_hsa_circ_353894,RMVar_hsa_circ_69805,RMVar_hsa_circ_194110,RMVar_hsa_circ_363447,RMVar_hsa_circ_291250,RMVar_hsa_circ_312685,RMVar_hsa_circ_276563,RMVar_hsa_circ_276657,RMVar_hsa_circ_275866,RMVar_hsa_circ_21381,RMVar_hsa_circ_194115,RMVar_hsa_circ_285792,RMVar_hsa_circ_310937,RMVar_hsa_circ_194112,RMVar_hsa_circ_194113,RMVar_hsa_circ_194111,RMVar_hsa_circ_356926,RMVar_hsa_circ_290880,RMVar_hsa_circ_288581,RMVar_hsa_circ_281045,RMVar_hsa_circ_285276,RMVar_hsa_circ_273262,RMVar_hsa_circ_194121,RMVar_hsa_circ_194125,RMVar_hsa_circ_119372,RMVar_hsa_circ_194126,RMVar_hsa_circ_194123,RMVar_hsa_circ_194124,RMVar_hsa_circ_194122,RMVar_hsa_circ_300968,RMVar_hsa_circ_194119,RMVar_hsa_circ_194120,RMVar_hsa_circ_313831,RMVar_hsa_circ_346878,RMVar_hsa_circ_368008,RMVar_hsa_circ_315612,RMVar_hsa_circ_301892,RMVar_hsa_circ_270348,RMVar_hsa_circ_288271,RMVar_hsa_circ_104307,RMVar_hsa_circ_194130,RMVar_hsa_circ_194132,RMVar_hsa_circ_194133,RMVar_hsa_circ_194131,RMVar_hsa_circ_194129 26271 RMVar_ID_26271 Human_SNP_ID_664220101 A-to-I Human chr19 + 34433740 34433740 34433740 CCAGCACTTTGAGAGACCAAGGCAGGAGGATCACTTGAGGTCAGGAGTTCGAGACCAACCTAGTC CCAGCACTTTGAGAGACCAAGGCAGGAGGATCGCTTGAGGTCAGGAGTTCGAGACCAACCTAGTC A G UBA2 Ensembl:ENSG00000126261 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs910917324 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25402963 RMVar_hsa_circ_93128,RMVar_hsa_circ_54140,RMVar_hsa_circ_125569,RMVar_hsa_circ_194114,RMVar_hsa_circ_279072,RMVar_hsa_circ_353894,RMVar_hsa_circ_69805,RMVar_hsa_circ_194110,RMVar_hsa_circ_363447,RMVar_hsa_circ_291250,RMVar_hsa_circ_312685,RMVar_hsa_circ_276563,RMVar_hsa_circ_276657,RMVar_hsa_circ_275866,RMVar_hsa_circ_21381,RMVar_hsa_circ_194115,RMVar_hsa_circ_285792,RMVar_hsa_circ_310937,RMVar_hsa_circ_194112,RMVar_hsa_circ_194113,RMVar_hsa_circ_194111,RMVar_hsa_circ_356926,RMVar_hsa_circ_290880,RMVar_hsa_circ_288581,RMVar_hsa_circ_281045,RMVar_hsa_circ_285276,RMVar_hsa_circ_273262,RMVar_hsa_circ_194121,RMVar_hsa_circ_194125,RMVar_hsa_circ_119372,RMVar_hsa_circ_194126,RMVar_hsa_circ_194123,RMVar_hsa_circ_194124,RMVar_hsa_circ_194122,RMVar_hsa_circ_300968,RMVar_hsa_circ_194119,RMVar_hsa_circ_194120,RMVar_hsa_circ_313831,RMVar_hsa_circ_346878,RMVar_hsa_circ_368008,RMVar_hsa_circ_315612,RMVar_hsa_circ_301892,RMVar_hsa_circ_270348,RMVar_hsa_circ_288271,RMVar_hsa_circ_104307,RMVar_hsa_circ_194130,RMVar_hsa_circ_194132,RMVar_hsa_circ_194133,RMVar_hsa_circ_194131,RMVar_hsa_circ_194129 26272 RMVar_ID_26272 Human_SNP_ID_664220110 A-to-I Human chr19 + 34433769 34433769 34433769 ATCACTTGAGGTCAGGAGTTCGAGACCAACCTAGTCAACATGGTGAAACCGTCTCTACCAAAAAA ATCACTTGAGGTCAGGAGTTCGAGACCAACCTGGTCAACATGGTGAAACCGTCTCTACCAAAAAA A G UBA2 Ensembl:ENSG00000126261 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1308958690 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93128,RMVar_hsa_circ_54140,RMVar_hsa_circ_125569,RMVar_hsa_circ_194114,RMVar_hsa_circ_279072,RMVar_hsa_circ_353894,RMVar_hsa_circ_69805,RMVar_hsa_circ_194110,RMVar_hsa_circ_363447,RMVar_hsa_circ_291250,RMVar_hsa_circ_312685,RMVar_hsa_circ_276563,RMVar_hsa_circ_276657,RMVar_hsa_circ_275866,RMVar_hsa_circ_21381,RMVar_hsa_circ_194115,RMVar_hsa_circ_285792,RMVar_hsa_circ_310937,RMVar_hsa_circ_194112,RMVar_hsa_circ_194113,RMVar_hsa_circ_194111,RMVar_hsa_circ_356926,RMVar_hsa_circ_290880,RMVar_hsa_circ_288581,RMVar_hsa_circ_281045,RMVar_hsa_circ_285276,RMVar_hsa_circ_273262,RMVar_hsa_circ_194121,RMVar_hsa_circ_194125,RMVar_hsa_circ_119372,RMVar_hsa_circ_194126,RMVar_hsa_circ_194123,RMVar_hsa_circ_194124,RMVar_hsa_circ_194122,RMVar_hsa_circ_300968,RMVar_hsa_circ_194119,RMVar_hsa_circ_194120,RMVar_hsa_circ_313831,RMVar_hsa_circ_346878,RMVar_hsa_circ_368008,RMVar_hsa_circ_315612,RMVar_hsa_circ_301892,RMVar_hsa_circ_270348,RMVar_hsa_circ_288271,RMVar_hsa_circ_104307,RMVar_hsa_circ_194130,RMVar_hsa_circ_194132,RMVar_hsa_circ_194133,RMVar_hsa_circ_194131,RMVar_hsa_circ_194129 26273 RMVar_ID_26273 Human_SNP_ID_664220126 A-to-I Human chr19 + 34433806 34433806 34433806 ACATGGTGAAACCGTCTCTACCAAAAAACACAAAAATTAGCCGGTGTGGTGGCATGTGCCTGTAG ACATGGTGAAACCGTCTCTACCAAAAAACACAGAAATTAGCCGGTGTGGTGGCATGTGCCTGTAG A G UBA2 Ensembl:ENSG00000126261 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs904783948 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93128,RMVar_hsa_circ_54140,RMVar_hsa_circ_125569,RMVar_hsa_circ_194114,RMVar_hsa_circ_279072,RMVar_hsa_circ_353894,RMVar_hsa_circ_69805,RMVar_hsa_circ_194110,RMVar_hsa_circ_363447,RMVar_hsa_circ_291250,RMVar_hsa_circ_312685,RMVar_hsa_circ_276563,RMVar_hsa_circ_276657,RMVar_hsa_circ_275866,RMVar_hsa_circ_21381,RMVar_hsa_circ_194115,RMVar_hsa_circ_285792,RMVar_hsa_circ_310937,RMVar_hsa_circ_194112,RMVar_hsa_circ_194113,RMVar_hsa_circ_194111,RMVar_hsa_circ_356926,RMVar_hsa_circ_290880,RMVar_hsa_circ_288581,RMVar_hsa_circ_281045,RMVar_hsa_circ_285276,RMVar_hsa_circ_273262,RMVar_hsa_circ_194121,RMVar_hsa_circ_194125,RMVar_hsa_circ_119372,RMVar_hsa_circ_194126,RMVar_hsa_circ_194123,RMVar_hsa_circ_194124,RMVar_hsa_circ_194122,RMVar_hsa_circ_300968,RMVar_hsa_circ_194119,RMVar_hsa_circ_194120,RMVar_hsa_circ_313831,RMVar_hsa_circ_346878,RMVar_hsa_circ_368008,RMVar_hsa_circ_315612,RMVar_hsa_circ_301892,RMVar_hsa_circ_270348,RMVar_hsa_circ_288271,RMVar_hsa_circ_104307,RMVar_hsa_circ_194130,RMVar_hsa_circ_194132,RMVar_hsa_circ_194133,RMVar_hsa_circ_194131,RMVar_hsa_circ_194129 26274 RMVar_ID_26274 Human_SNP_ID_664221323 A-to-I Human chr19 + 34437961 34437961 34437961 CCTGTAATCCCAGCTCTTTGGGAGCCTGAGGCAGGAGAATTGCTTGAACCTGGGAGGCGGAGATT CCTGTAATCCCAGCTCTTTGGGAGCCTGAGGCGGGAGAATTGCTTGAACCTGGGAGGCGGAGATT A G UBA2 Ensembl:ENSG00000126261 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1431350326 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25444310 RMVar_hsa_circ_93128,RMVar_hsa_circ_54140,RMVar_hsa_circ_125569,RMVar_hsa_circ_194114,RMVar_hsa_circ_279072,RMVar_hsa_circ_353894,RMVar_hsa_circ_194110,RMVar_hsa_circ_363447,RMVar_hsa_circ_291250,RMVar_hsa_circ_312685,RMVar_hsa_circ_276657,RMVar_hsa_circ_275866,RMVar_hsa_circ_21381,RMVar_hsa_circ_285792,RMVar_hsa_circ_310937,RMVar_hsa_circ_194112,RMVar_hsa_circ_194113,RMVar_hsa_circ_194111,RMVar_hsa_circ_356926,RMVar_hsa_circ_290880,RMVar_hsa_circ_288581,RMVar_hsa_circ_281045,RMVar_hsa_circ_273262,RMVar_hsa_circ_194121,RMVar_hsa_circ_194125,RMVar_hsa_circ_119372,RMVar_hsa_circ_194123,RMVar_hsa_circ_194124,RMVar_hsa_circ_194122,RMVar_hsa_circ_300968,RMVar_hsa_circ_194119,RMVar_hsa_circ_194120,RMVar_hsa_circ_346878,RMVar_hsa_circ_368008,RMVar_hsa_circ_315612,RMVar_hsa_circ_301892,RMVar_hsa_circ_270348,RMVar_hsa_circ_288271,RMVar_hsa_circ_104307,RMVar_hsa_circ_28673,RMVar_hsa_circ_274934,RMVar_hsa_circ_194130,RMVar_hsa_circ_194132,RMVar_hsa_circ_194133,RMVar_hsa_circ_194131,RMVar_hsa_circ_300327,RMVar_hsa_circ_194129,RMVar_hsa_circ_320255,RMVar_hsa_circ_279648,RMVar_hsa_circ_96875,RMVar_hsa_circ_271877,RMVar_hsa_circ_76037,RMVar_hsa_circ_194136,RMVar_hsa_circ_194138,RMVar_hsa_circ_194139,RMVar_hsa_circ_194140,RMVar_hsa_circ_194137,RMVar_hsa_circ_194134,RMVar_hsa_circ_194135 26275 RMVar_ID_26275 Human_SNP_ID_664221324 A-to-I Human chr19 + 34437964 34437964 34437964 GTAATCCCAGCTCTTTGGGAGCCTGAGGCAGGAGAATTGCTTGAACCTGGGAGGCGGAGATTGCA GTAATCCCAGCTCTTTGGGAGCCTGAGGCAGGTGAATTGCTTGAACCTGGGAGGCGGAGATTGCA A T UBA2 Ensembl:ENSG00000126261 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1019599779 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25403055 RMVar_hsa_circ_93128,RMVar_hsa_circ_54140,RMVar_hsa_circ_125569,RMVar_hsa_circ_194114,RMVar_hsa_circ_279072,RMVar_hsa_circ_353894,RMVar_hsa_circ_194110,RMVar_hsa_circ_363447,RMVar_hsa_circ_291250,RMVar_hsa_circ_312685,RMVar_hsa_circ_276657,RMVar_hsa_circ_275866,RMVar_hsa_circ_21381,RMVar_hsa_circ_285792,RMVar_hsa_circ_310937,RMVar_hsa_circ_194112,RMVar_hsa_circ_194113,RMVar_hsa_circ_194111,RMVar_hsa_circ_356926,RMVar_hsa_circ_290880,RMVar_hsa_circ_288581,RMVar_hsa_circ_281045,RMVar_hsa_circ_273262,RMVar_hsa_circ_194121,RMVar_hsa_circ_194125,RMVar_hsa_circ_119372,RMVar_hsa_circ_194123,RMVar_hsa_circ_194124,RMVar_hsa_circ_194122,RMVar_hsa_circ_300968,RMVar_hsa_circ_194119,RMVar_hsa_circ_194120,RMVar_hsa_circ_346878,RMVar_hsa_circ_368008,RMVar_hsa_circ_315612,RMVar_hsa_circ_301892,RMVar_hsa_circ_270348,RMVar_hsa_circ_288271,RMVar_hsa_circ_104307,RMVar_hsa_circ_28673,RMVar_hsa_circ_274934,RMVar_hsa_circ_194130,RMVar_hsa_circ_194132,RMVar_hsa_circ_194133,RMVar_hsa_circ_194131,RMVar_hsa_circ_300327,RMVar_hsa_circ_194129,RMVar_hsa_circ_320255,RMVar_hsa_circ_279648,RMVar_hsa_circ_96875,RMVar_hsa_circ_271877,RMVar_hsa_circ_76037,RMVar_hsa_circ_194136,RMVar_hsa_circ_194138,RMVar_hsa_circ_194139,RMVar_hsa_circ_194140,RMVar_hsa_circ_194137,RMVar_hsa_circ_194134,RMVar_hsa_circ_194135 26276 RMVar_ID_26276 Human_SNP_ID_664221607 A-to-I Human chr19 + 34439032 34439032 34439032 GGAGTTTGAGACCAGCGTGGCCAGCATGGTGAAACACATCTCTACTAAAAATACAAAAATTAGTT GGAGTTTGAGACCAGCGTGGCCAGCATGGTGAGACACATCTCTACTAAAAATACAAAAATTAGTT A G UBA2 Ensembl:ENSG00000126261 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs928627298 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54140,RMVar_hsa_circ_125569,RMVar_hsa_circ_353894,RMVar_hsa_circ_363447,RMVar_hsa_circ_291250,RMVar_hsa_circ_312685,RMVar_hsa_circ_276657,RMVar_hsa_circ_275866,RMVar_hsa_circ_21381,RMVar_hsa_circ_310937,RMVar_hsa_circ_194112,RMVar_hsa_circ_194113,RMVar_hsa_circ_194111,RMVar_hsa_circ_356926,RMVar_hsa_circ_290880,RMVar_hsa_circ_288581,RMVar_hsa_circ_281045,RMVar_hsa_circ_273262,RMVar_hsa_circ_194121,RMVar_hsa_circ_119372,RMVar_hsa_circ_194123,RMVar_hsa_circ_194124,RMVar_hsa_circ_194122,RMVar_hsa_circ_300968,RMVar_hsa_circ_194119,RMVar_hsa_circ_194120,RMVar_hsa_circ_346878,RMVar_hsa_circ_368008,RMVar_hsa_circ_315612,RMVar_hsa_circ_301892,RMVar_hsa_circ_288271,RMVar_hsa_circ_104307,RMVar_hsa_circ_120108,RMVar_hsa_circ_28673,RMVar_hsa_circ_274934,RMVar_hsa_circ_194130,RMVar_hsa_circ_194132,RMVar_hsa_circ_194133,RMVar_hsa_circ_194131,RMVar_hsa_circ_300327,RMVar_hsa_circ_320255,RMVar_hsa_circ_279648,RMVar_hsa_circ_96875,RMVar_hsa_circ_76037,RMVar_hsa_circ_194136,RMVar_hsa_circ_194138,RMVar_hsa_circ_194139,RMVar_hsa_circ_194137,RMVar_hsa_circ_317552,RMVar_hsa_circ_194134,RMVar_hsa_circ_194135,RMVar_hsa_circ_372722,RMVar_hsa_circ_376106,RMVar_hsa_circ_325763,RMVar_hsa_circ_274439,RMVar_hsa_circ_283324,RMVar_hsa_circ_194143,RMVar_hsa_circ_194147,RMVar_hsa_circ_76308,RMVar_hsa_circ_77704,RMVar_hsa_circ_194148,RMVar_hsa_circ_194145,RMVar_hsa_circ_194146,RMVar_hsa_circ_194144,RMVar_hsa_circ_194141,RMVar_hsa_circ_194142 26277 RMVar_ID_26277 Human_SNP_ID_664222080 A-to-I Human chr19 + 34440731 34440731 34440731 GGTGGATCACCTGAGGTCAGGAGTTCAAGACCAACTTGGCCAATATGGCGAAATCCTGTCTCTAT GGTGGATCACCTGAGGTCAGGAGTTCAAGACCGACTTGGCCAATATGGCGAAATCCTGTCTCTAT A G UBA2 Ensembl:ENSG00000126261 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1039814431 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9916196,Human_RBP_ID_22970052 RMVar_hsa_circ_54140,RMVar_hsa_circ_125569,RMVar_hsa_circ_353894,RMVar_hsa_circ_363447,RMVar_hsa_circ_291250,RMVar_hsa_circ_312685,RMVar_hsa_circ_276657,RMVar_hsa_circ_275866,RMVar_hsa_circ_21381,RMVar_hsa_circ_310937,RMVar_hsa_circ_194112,RMVar_hsa_circ_194113,RMVar_hsa_circ_194111,RMVar_hsa_circ_356926,RMVar_hsa_circ_290880,RMVar_hsa_circ_288581,RMVar_hsa_circ_281045,RMVar_hsa_circ_273262,RMVar_hsa_circ_194121,RMVar_hsa_circ_119372,RMVar_hsa_circ_194123,RMVar_hsa_circ_194124,RMVar_hsa_circ_194122,RMVar_hsa_circ_300968,RMVar_hsa_circ_194119,RMVar_hsa_circ_194120,RMVar_hsa_circ_346878,RMVar_hsa_circ_368008,RMVar_hsa_circ_315612,RMVar_hsa_circ_301892,RMVar_hsa_circ_288271,RMVar_hsa_circ_104307,RMVar_hsa_circ_120108,RMVar_hsa_circ_28673,RMVar_hsa_circ_274934,RMVar_hsa_circ_194130,RMVar_hsa_circ_194132,RMVar_hsa_circ_194133,RMVar_hsa_circ_194131,RMVar_hsa_circ_300327,RMVar_hsa_circ_320255,RMVar_hsa_circ_279648,RMVar_hsa_circ_96875,RMVar_hsa_circ_76037,RMVar_hsa_circ_194136,RMVar_hsa_circ_194138,RMVar_hsa_circ_194139,RMVar_hsa_circ_194137,RMVar_hsa_circ_317552,RMVar_hsa_circ_194134,RMVar_hsa_circ_194135,RMVar_hsa_circ_372722,RMVar_hsa_circ_376106,RMVar_hsa_circ_325763,RMVar_hsa_circ_274439,RMVar_hsa_circ_283324,RMVar_hsa_circ_194143,RMVar_hsa_circ_194147,RMVar_hsa_circ_76308,RMVar_hsa_circ_77704,RMVar_hsa_circ_194148,RMVar_hsa_circ_194145,RMVar_hsa_circ_194146,RMVar_hsa_circ_194144,RMVar_hsa_circ_194141,RMVar_hsa_circ_194142 26278 RMVar_ID_26278 Human_SNP_ID_664222107 A-to-I Human chr19 + 34440803 34440803 34440803 ACAAAATTAGCCGGACATGGTGGTGGGCGCCTATAATCCCAGCTACTTGGGAGGCTGAGGCAGGA ACAAAATTAGCCGGACATGGTGGTGGGCGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGA A G UBA2 Ensembl:ENSG00000126261 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs902638719 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54140,RMVar_hsa_circ_125569,RMVar_hsa_circ_353894,RMVar_hsa_circ_363447,RMVar_hsa_circ_291250,RMVar_hsa_circ_312685,RMVar_hsa_circ_276657,RMVar_hsa_circ_275866,RMVar_hsa_circ_21381,RMVar_hsa_circ_310937,RMVar_hsa_circ_194112,RMVar_hsa_circ_194113,RMVar_hsa_circ_194111,RMVar_hsa_circ_356926,RMVar_hsa_circ_290880,RMVar_hsa_circ_288581,RMVar_hsa_circ_281045,RMVar_hsa_circ_273262,RMVar_hsa_circ_194121,RMVar_hsa_circ_119372,RMVar_hsa_circ_194123,RMVar_hsa_circ_194124,RMVar_hsa_circ_194122,RMVar_hsa_circ_300968,RMVar_hsa_circ_194119,RMVar_hsa_circ_194120,RMVar_hsa_circ_346878,RMVar_hsa_circ_368008,RMVar_hsa_circ_315612,RMVar_hsa_circ_301892,RMVar_hsa_circ_288271,RMVar_hsa_circ_104307,RMVar_hsa_circ_120108,RMVar_hsa_circ_28673,RMVar_hsa_circ_274934,RMVar_hsa_circ_194130,RMVar_hsa_circ_194132,RMVar_hsa_circ_194133,RMVar_hsa_circ_194131,RMVar_hsa_circ_300327,RMVar_hsa_circ_320255,RMVar_hsa_circ_279648,RMVar_hsa_circ_96875,RMVar_hsa_circ_76037,RMVar_hsa_circ_194136,RMVar_hsa_circ_194138,RMVar_hsa_circ_194139,RMVar_hsa_circ_194137,RMVar_hsa_circ_317552,RMVar_hsa_circ_194134,RMVar_hsa_circ_194135,RMVar_hsa_circ_372722,RMVar_hsa_circ_376106,RMVar_hsa_circ_325763,RMVar_hsa_circ_274439,RMVar_hsa_circ_283324,RMVar_hsa_circ_194143,RMVar_hsa_circ_194147,RMVar_hsa_circ_76308,RMVar_hsa_circ_77704,RMVar_hsa_circ_194148,RMVar_hsa_circ_194145,RMVar_hsa_circ_194146,RMVar_hsa_circ_194144,RMVar_hsa_circ_194141,RMVar_hsa_circ_194142 26279 RMVar_ID_26279 Human_SNP_ID_664222264 A-to-I Human chr19 + 34441334 34441334 34441334 AAAATTAGCCGGATGTGGTGGTGGGTGCCTGTAGTCCCAGCTGCTCAGGAGGCTGAGGCAGGAGA AAAATTAGCCGGATGTGGTGGTGGGTGCCTGTGGTCCCAGCTGCTCAGGAGGCTGAGGCAGGAGA A G UBA2 Ensembl:ENSG00000126261 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1158667095 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54140,RMVar_hsa_circ_125569,RMVar_hsa_circ_353894,RMVar_hsa_circ_363447,RMVar_hsa_circ_291250,RMVar_hsa_circ_312685,RMVar_hsa_circ_276657,RMVar_hsa_circ_275866,RMVar_hsa_circ_21381,RMVar_hsa_circ_310937,RMVar_hsa_circ_194112,RMVar_hsa_circ_194113,RMVar_hsa_circ_194111,RMVar_hsa_circ_356926,RMVar_hsa_circ_290880,RMVar_hsa_circ_288581,RMVar_hsa_circ_281045,RMVar_hsa_circ_273262,RMVar_hsa_circ_194121,RMVar_hsa_circ_119372,RMVar_hsa_circ_194123,RMVar_hsa_circ_194124,RMVar_hsa_circ_194122,RMVar_hsa_circ_300968,RMVar_hsa_circ_194119,RMVar_hsa_circ_194120,RMVar_hsa_circ_346878,RMVar_hsa_circ_368008,RMVar_hsa_circ_315612,RMVar_hsa_circ_301892,RMVar_hsa_circ_288271,RMVar_hsa_circ_104307,RMVar_hsa_circ_120108,RMVar_hsa_circ_28673,RMVar_hsa_circ_274934,RMVar_hsa_circ_194130,RMVar_hsa_circ_194132,RMVar_hsa_circ_194133,RMVar_hsa_circ_194131,RMVar_hsa_circ_300327,RMVar_hsa_circ_320255,RMVar_hsa_circ_279648,RMVar_hsa_circ_96875,RMVar_hsa_circ_76037,RMVar_hsa_circ_194136,RMVar_hsa_circ_194138,RMVar_hsa_circ_194139,RMVar_hsa_circ_194137,RMVar_hsa_circ_317552,RMVar_hsa_circ_194134,RMVar_hsa_circ_194135,RMVar_hsa_circ_372722,RMVar_hsa_circ_376106,RMVar_hsa_circ_325763,RMVar_hsa_circ_274439,RMVar_hsa_circ_283324,RMVar_hsa_circ_194143,RMVar_hsa_circ_194147,RMVar_hsa_circ_76308,RMVar_hsa_circ_77704,RMVar_hsa_circ_194148,RMVar_hsa_circ_194145,RMVar_hsa_circ_194146,RMVar_hsa_circ_194144,RMVar_hsa_circ_194141,RMVar_hsa_circ_194142 26280 RMVar_ID_26280 Human_SNP_ID_664222395 A-to-I Human chr19 + 34441800 34441800 34441800 AAAATTAGTGGGGTGTGGTGGCACACGCCTGTAGTCCCACCTACTCGGGAGGCTGAGCCATGAGA AAAATTAGTGGGGTGTGGTGGCACACGCCTGTGGTCCCACCTACTCGGGAGGCTGAGCCATGAGA A G UBA2 Ensembl:ENSG00000126261 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1344778999 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13433357 RMVar_hsa_circ_54140,RMVar_hsa_circ_125569,RMVar_hsa_circ_353894,RMVar_hsa_circ_363447,RMVar_hsa_circ_291250,RMVar_hsa_circ_312685,RMVar_hsa_circ_276657,RMVar_hsa_circ_275866,RMVar_hsa_circ_21381,RMVar_hsa_circ_310937,RMVar_hsa_circ_194112,RMVar_hsa_circ_194113,RMVar_hsa_circ_194111,RMVar_hsa_circ_356926,RMVar_hsa_circ_290880,RMVar_hsa_circ_288581,RMVar_hsa_circ_281045,RMVar_hsa_circ_273262,RMVar_hsa_circ_194121,RMVar_hsa_circ_119372,RMVar_hsa_circ_194123,RMVar_hsa_circ_194124,RMVar_hsa_circ_194122,RMVar_hsa_circ_300968,RMVar_hsa_circ_194119,RMVar_hsa_circ_194120,RMVar_hsa_circ_346878,RMVar_hsa_circ_368008,RMVar_hsa_circ_315612,RMVar_hsa_circ_301892,RMVar_hsa_circ_288271,RMVar_hsa_circ_104307,RMVar_hsa_circ_120108,RMVar_hsa_circ_28673,RMVar_hsa_circ_274934,RMVar_hsa_circ_194130,RMVar_hsa_circ_194132,RMVar_hsa_circ_194133,RMVar_hsa_circ_194131,RMVar_hsa_circ_300327,RMVar_hsa_circ_320255,RMVar_hsa_circ_279648,RMVar_hsa_circ_96875,RMVar_hsa_circ_76037,RMVar_hsa_circ_194136,RMVar_hsa_circ_194138,RMVar_hsa_circ_194139,RMVar_hsa_circ_194137,RMVar_hsa_circ_317552,RMVar_hsa_circ_194134,RMVar_hsa_circ_194135,RMVar_hsa_circ_372722,RMVar_hsa_circ_376106,RMVar_hsa_circ_325763,RMVar_hsa_circ_274439,RMVar_hsa_circ_283324,RMVar_hsa_circ_194143,RMVar_hsa_circ_194147,RMVar_hsa_circ_76308,RMVar_hsa_circ_77704,RMVar_hsa_circ_194148,RMVar_hsa_circ_194145,RMVar_hsa_circ_194146,RMVar_hsa_circ_194144,RMVar_hsa_circ_194141,RMVar_hsa_circ_194142 26281 RMVar_ID_26281 Human_SNP_ID_664222920 A-to-I Human chr19 + 34443714 34443714 34443714 TGCCTGCCTCAGCCTCCCAAAATGTTGGGATTAAAGGTGTGAGCCACTGCGCCCAGCCAGTTGTT TGCCTGCCTCAGCCTCCCAAAATGTTGGGATTGAAGGTGTGAGCCACTGCGCCCAGCCAGTTGTT A G UBA2 Ensembl:ENSG00000126261 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1487530572 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23176212,Human_RBP_ID_25403182 RMVar_hsa_circ_54140,RMVar_hsa_circ_125569,RMVar_hsa_circ_353894,RMVar_hsa_circ_363447,RMVar_hsa_circ_291250,RMVar_hsa_circ_312685,RMVar_hsa_circ_276657,RMVar_hsa_circ_275866,RMVar_hsa_circ_21381,RMVar_hsa_circ_310937,RMVar_hsa_circ_194112,RMVar_hsa_circ_194113,RMVar_hsa_circ_194111,RMVar_hsa_circ_356926,RMVar_hsa_circ_290880,RMVar_hsa_circ_288581,RMVar_hsa_circ_281045,RMVar_hsa_circ_273262,RMVar_hsa_circ_194121,RMVar_hsa_circ_119372,RMVar_hsa_circ_194123,RMVar_hsa_circ_194124,RMVar_hsa_circ_194122,RMVar_hsa_circ_300968,RMVar_hsa_circ_194119,RMVar_hsa_circ_194120,RMVar_hsa_circ_346878,RMVar_hsa_circ_368008,RMVar_hsa_circ_315612,RMVar_hsa_circ_301892,RMVar_hsa_circ_288271,RMVar_hsa_circ_104307,RMVar_hsa_circ_120108,RMVar_hsa_circ_28673,RMVar_hsa_circ_274934,RMVar_hsa_circ_194130,RMVar_hsa_circ_194132,RMVar_hsa_circ_194133,RMVar_hsa_circ_194131,RMVar_hsa_circ_300327,RMVar_hsa_circ_320255,RMVar_hsa_circ_279648,RMVar_hsa_circ_96875,RMVar_hsa_circ_76037,RMVar_hsa_circ_194136,RMVar_hsa_circ_194138,RMVar_hsa_circ_194139,RMVar_hsa_circ_194137,RMVar_hsa_circ_317552,RMVar_hsa_circ_194134,RMVar_hsa_circ_194135,RMVar_hsa_circ_372722,RMVar_hsa_circ_376106,RMVar_hsa_circ_325763,RMVar_hsa_circ_274439,RMVar_hsa_circ_283324,RMVar_hsa_circ_194143,RMVar_hsa_circ_194147,RMVar_hsa_circ_76308,RMVar_hsa_circ_77704,RMVar_hsa_circ_194148,RMVar_hsa_circ_194145,RMVar_hsa_circ_194146,RMVar_hsa_circ_194144,RMVar_hsa_circ_194141,RMVar_hsa_circ_194142 26282 RMVar_ID_26282 Human_SNP_ID_664223105 A-to-I Human chr19 + 34444137 34444137 34444137 TGGAGTACAATGGTATAATCTCGGCTCACTGCAACCTCCGCCTTCTGGGTTCAAATGATTCTCCT TGGAGTACAATGGTATAATCTCGGCTCACTGCGACCTCCGCCTTCTGGGTTCAAATGATTCTCCT A G UBA2 Ensembl:ENSG00000126261 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1435378979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6745015 RMVar_hsa_circ_9877,RMVar_hsa_circ_54140,RMVar_hsa_circ_125569,RMVar_hsa_circ_353894,RMVar_hsa_circ_291250,RMVar_hsa_circ_312685,RMVar_hsa_circ_276657,RMVar_hsa_circ_275866,RMVar_hsa_circ_21381,RMVar_hsa_circ_310937,RMVar_hsa_circ_194112,RMVar_hsa_circ_194113,RMVar_hsa_circ_194111,RMVar_hsa_circ_356926,RMVar_hsa_circ_288581,RMVar_hsa_circ_281045,RMVar_hsa_circ_273262,RMVar_hsa_circ_194121,RMVar_hsa_circ_119372,RMVar_hsa_circ_194123,RMVar_hsa_circ_194122,RMVar_hsa_circ_194119,RMVar_hsa_circ_194120,RMVar_hsa_circ_346878,RMVar_hsa_circ_368008,RMVar_hsa_circ_315612,RMVar_hsa_circ_301892,RMVar_hsa_circ_288271,RMVar_hsa_circ_104307,RMVar_hsa_circ_120108,RMVar_hsa_circ_28673,RMVar_hsa_circ_274934,RMVar_hsa_circ_194132,RMVar_hsa_circ_194133,RMVar_hsa_circ_194131,RMVar_hsa_circ_320255,RMVar_hsa_circ_279648,RMVar_hsa_circ_96875,RMVar_hsa_circ_76037,RMVar_hsa_circ_194136,RMVar_hsa_circ_194138,RMVar_hsa_circ_194137,RMVar_hsa_circ_317552,RMVar_hsa_circ_194134,RMVar_hsa_circ_194135,RMVar_hsa_circ_372722,RMVar_hsa_circ_376106,RMVar_hsa_circ_325763,RMVar_hsa_circ_274439,RMVar_hsa_circ_194143,RMVar_hsa_circ_194147,RMVar_hsa_circ_76308,RMVar_hsa_circ_77704,RMVar_hsa_circ_194145,RMVar_hsa_circ_194146,RMVar_hsa_circ_194144,RMVar_hsa_circ_194141,RMVar_hsa_circ_194142,RMVar_hsa_circ_278940,RMVar_hsa_circ_321941,RMVar_hsa_circ_368603,RMVar_hsa_circ_302325,RMVar_hsa_circ_105142,RMVar_hsa_circ_194150,RMVar_hsa_circ_194152,RMVar_hsa_circ_194153,RMVar_hsa_circ_194154,RMVar_hsa_circ_194151 26283 RMVar_ID_26283 Human_SNP_ID_664223276 A-to-I Human chr19 + 34444746 34444746 34444746 GGAAGATGGCTTGAGCCCAAGAGGTAGAAGCTACAGTGAGCCGAGATCTTAACACTGCACTCCAG GGAAGATGGCTTGAGCCCAAGAGGTAGAAGCTGCAGTGAGCCGAGATCTTAACACTGCACTCCAG A G UBA2 Ensembl:ENSG00000126261 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1033012425 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6745021,Human_RBP_ID_8255970,Human_RBP_ID_13433423 RMVar_hsa_circ_9877,RMVar_hsa_circ_54140,RMVar_hsa_circ_125569,RMVar_hsa_circ_353894,RMVar_hsa_circ_291250,RMVar_hsa_circ_312685,RMVar_hsa_circ_276657,RMVar_hsa_circ_275866,RMVar_hsa_circ_21381,RMVar_hsa_circ_310937,RMVar_hsa_circ_194112,RMVar_hsa_circ_194113,RMVar_hsa_circ_194111,RMVar_hsa_circ_356926,RMVar_hsa_circ_288581,RMVar_hsa_circ_281045,RMVar_hsa_circ_273262,RMVar_hsa_circ_194121,RMVar_hsa_circ_119372,RMVar_hsa_circ_194123,RMVar_hsa_circ_194122,RMVar_hsa_circ_194119,RMVar_hsa_circ_194120,RMVar_hsa_circ_346878,RMVar_hsa_circ_368008,RMVar_hsa_circ_315612,RMVar_hsa_circ_301892,RMVar_hsa_circ_288271,RMVar_hsa_circ_104307,RMVar_hsa_circ_120108,RMVar_hsa_circ_28673,RMVar_hsa_circ_274934,RMVar_hsa_circ_194132,RMVar_hsa_circ_194133,RMVar_hsa_circ_194131,RMVar_hsa_circ_320255,RMVar_hsa_circ_279648,RMVar_hsa_circ_96875,RMVar_hsa_circ_76037,RMVar_hsa_circ_194136,RMVar_hsa_circ_194138,RMVar_hsa_circ_194137,RMVar_hsa_circ_317552,RMVar_hsa_circ_194134,RMVar_hsa_circ_194135,RMVar_hsa_circ_372722,RMVar_hsa_circ_376106,RMVar_hsa_circ_325763,RMVar_hsa_circ_274439,RMVar_hsa_circ_194143,RMVar_hsa_circ_194147,RMVar_hsa_circ_76308,RMVar_hsa_circ_77704,RMVar_hsa_circ_194145,RMVar_hsa_circ_194146,RMVar_hsa_circ_194144,RMVar_hsa_circ_194141,RMVar_hsa_circ_194142,RMVar_hsa_circ_278940,RMVar_hsa_circ_321941,RMVar_hsa_circ_368603,RMVar_hsa_circ_302325,RMVar_hsa_circ_105142,RMVar_hsa_circ_194150,RMVar_hsa_circ_194152,RMVar_hsa_circ_194153,RMVar_hsa_circ_194154,RMVar_hsa_circ_194151 26284 RMVar_ID_26284 Human_SNP_ID_664226650 A-to-I Human chr19 + 34456627 34456627 34456627 TCACCCAGGCTAGAGTGCAGTGGCGCGATCTCAGCTCACTGCAACCTCCACCTCCCAAGTAGAAG TCACCCAGGCTAGAGTGCAGTGGCGCGATCTCTGCTCACTGCAACCTCCACCTCCCAAGTAGAAG A T UBA2 Ensembl:ENSG00000126261 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982553988 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9877,RMVar_hsa_circ_353894,RMVar_hsa_circ_276657,RMVar_hsa_circ_275866,RMVar_hsa_circ_194112,RMVar_hsa_circ_194111,RMVar_hsa_circ_288581,RMVar_hsa_circ_281045,RMVar_hsa_circ_273262,RMVar_hsa_circ_194121,RMVar_hsa_circ_119372,RMVar_hsa_circ_194119,RMVar_hsa_circ_194120,RMVar_hsa_circ_315612,RMVar_hsa_circ_301892,RMVar_hsa_circ_288271,RMVar_hsa_circ_104307,RMVar_hsa_circ_120108,RMVar_hsa_circ_28673,RMVar_hsa_circ_274934,RMVar_hsa_circ_194132,RMVar_hsa_circ_194133,RMVar_hsa_circ_320255,RMVar_hsa_circ_96875,RMVar_hsa_circ_194136,RMVar_hsa_circ_194134,RMVar_hsa_circ_194135,RMVar_hsa_circ_376106,RMVar_hsa_circ_325763,RMVar_hsa_circ_194143,RMVar_hsa_circ_76308,RMVar_hsa_circ_194141,RMVar_hsa_circ_194142,RMVar_hsa_circ_368603,RMVar_hsa_circ_302325,RMVar_hsa_circ_119260,RMVar_hsa_circ_194153,RMVar_hsa_circ_194154,RMVar_hsa_circ_194156,RMVar_hsa_circ_296012,RMVar_hsa_circ_287494,RMVar_hsa_circ_194157,RMVar_hsa_circ_284270,RMVar_hsa_circ_297766,RMVar_hsa_circ_277644,RMVar_hsa_circ_285296,RMVar_hsa_circ_194158,RMVar_hsa_circ_194160,RMVar_hsa_circ_194161,RMVar_hsa_circ_194159,RMVar_hsa_circ_290446,RMVar_hsa_circ_287433,RMVar_hsa_circ_194164,RMVar_hsa_circ_194165,RMVar_hsa_circ_194163,RMVar_hsa_circ_103420,RMVar_hsa_circ_194169,RMVar_hsa_circ_276432,RMVar_hsa_circ_309064,RMVar_hsa_circ_353971,RMVar_hsa_circ_127508,RMVar_hsa_circ_194167,RMVar_hsa_circ_194168,RMVar_hsa_circ_194166,RMVar_hsa_circ_194170 26285 RMVar_ID_26285 Human_SNP_ID_664230702 A-to-I Human chr19 + 34471436 34471436 34471436 ACTTTGAGAGGCTGAGGCAGGAGGATCGTTTGAGCCCAGGAGTTTGAGACCAGCCTGAGCAACAT ACTTTGAGAGGCTGAGGCAGGAGGATCGTTTGGGCCCAGGAGTTTGAGACCAGCCTGAGCAACAT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946553915 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_194179 26286 RMVar_ID_26286 Human_SNP_ID_664238280 A-to-I Human chr19 + 34497043 34497041 34497044 CACCACCACACCCGGCTAGTTTTTGTGTTTTTAGTAGTGACAGGGTTTCACCATGTTGGCTGGGC CACCACCACACCCGGCTAGTTTTTGTGTTTT___TAGTGACAGGGTTTCACCATGTTGGCTGGGC TTAG T WTIP Ensembl:ENSG00000142279 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1480740183 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_125764,RMVar_hsa_circ_194182 26287 RMVar_ID_26287 Human_SNP_ID_664272897 A-to-I Human chr19 - 34633025 34633025 34633025 ACCAGGCAGGGCAGAGTAAGCAGCTTGTGATTAGCTAGTTTGCATAATTTCAGCAGGCTTTGGCC ACCAGGCAGGGCAGAGTAAGCAGCTTGTGATTGGCTAGTTTGCATAATTTCAGCAGGCTTTGGCC T C SCGB2B2 Ensembl:ENSG00000205209 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs961684569 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118266,RMVar_hsa_circ_194186 26288 RMVar_ID_26288 Human_SNP_ID_664299622 A-to-I Human chr19 + 34742584 34742584 34742584 ACACATCAGAAGATTAATGGTAGAACAACCTGAAGGATTTAGGAGTTATGTGTAAATCTTTGCAG ACACATCAGAAGATTAATGGTAGAACAACCTGGAGGATTTAGGAGTTATGTGTAAATCTTTGCAG A G ZNF181 Ensembl:ENSG00000197841 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1257048003 Functional Loss SNV dbSNP153 33..33 33 - - - 26289 RMVar_ID_26289 Human_SNP_ID_664406768 A-to-I Human chr19 + 35160405 35160405 35160405 GAGTTTTGCTCTTGTTGCCCAGGTCGCTGTGCAATGGTGCAATCTCGGCTCACCACAACCTCTGC GAGTTTTGCTCTTGTTGCCCAGGTCGCTGTGCGATGGTGCAATCTCGGCTCACCACAACCTCTGC A G FXYD5 Ensembl:ENSG00000089327 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs995684731 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122291,RMVar_hsa_circ_194216 26290 RMVar_ID_26290 Human_SNP_ID_664429634 A-to-I Human chr19 + 35252874 35252874 35252874 ATGTCTACAAAAATTTTAAAAATTTAAAAATTAGCTGGGCATGGTGGCATGTGCCTGTGGTCCCG ATGTCTACAAAAATTTTAAAAATTTAAAAATTCGCTGGGCATGGTGGCATGTGCCTGTGGTCCCG A C LSR Ensembl:ENSG00000105699 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1480830982 Functional Loss SNV dbSNP153 33..33 33 - - - 26291 RMVar_ID_26291 Human_SNP_ID_664432547 A-to-I Human chr19 + 35263473 35263473 35263473 AAACTCCCGGGTTCAAGCAGTCCTCCCGCCTCAGCCTCTGGAGCAGCTGGGACTGTAGGCACACA AAACTCCCGGGTTCAAGCAGTCCTCCCGCCTCGGCCTCTGGAGCAGCTGGGACTGTAGGCACACA A G AC002128.1,LSR Ensembl:ENSG00000268947,Ensembl:ENSG00000105699 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1276181468 Functional Loss SNV dbSNP153 33..33 33 - - - 26292 RMVar_ID_26292 Human_SNP_ID_664436915 A-to-I Human chr19 + 35274695 35274695 35274695 CCTGGTGGTACATGCCTGTAACAGTCCCAGCTACTTGGGAACCTGTGGTGGGAAGATGGCTTGAG CCTGGTGGTACATGCCTGTAACAGTCCCAGCTGCTTGGGAACCTGTGGTGGGAAGATGGCTTGAG A G USF2 Ensembl:ENSG00000105698 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1197841449 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13435813 RMVar_hsa_circ_27947,RMVar_hsa_circ_98702,RMVar_hsa_circ_194227 26293 RMVar_ID_26293 Human_SNP_ID_664445929 A-to-I Human chr19 + 35305848 35305848 35305848 GTGATGGCGCACACCTGCAGTTCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAGCCCG GTGATGGCGCACACCTGCAGTTCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAGCCCG A G MAG Ensembl:ENSG00000105695 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs573037612 Functional Loss SNV dbSNP153 33..33 33 - - - 26294 RMVar_ID_26294 Human_SNP_ID_664445931 A-to-I Human chr19 + 35305861 35305861 35305861 CCTGCAGTTCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAGCCCGGGGGGTGGAGGTT CCTGCAGTTCCAGCTACTCAGGAGGCTGAGGCGGGAGAATCGCTTGAGCCCGGGGGGTGGAGGTT A G MAG Ensembl:ENSG00000105695 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559112878 Functional Loss SNV dbSNP153 33..33 33 - - - 26295 RMVar_ID_26295 Human_SNP_ID_664445935 A-to-I Human chr19 + 35305875 35305875 35305875 TACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAGCCCGGGGGGTGGAGGTTGCAGTGAGCTGAGA TACTCAGGAGGCTGAGGCAGGAGAATCGCTTGGGCCCGGGGGGTGGAGGTTGCAGTGAGCTGAGA A G MAG Ensembl:ENSG00000105695 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985971716 Functional Loss SNV dbSNP153 33..33 33 - - - 26296 RMVar_ID_26296 Human_SNP_ID_664452114 A-to-I Human chr19 + 35330213 35330213 35330213 AACAAATCAGACGGGTGTGGTGGCACATGCCTATAGTCCCAGCTACTCAGGAGGCTGAGGCAGGA AACAAATCAGACGGGTGTGGTGGCACATGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGA A G CD22 Ensembl:ENSG00000012124 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041439477 Functional Loss SNV dbSNP153 33..33 33 - - - 26297 RMVar_ID_26297 Human_SNP_ID_664452267 A-to-I Human chr19 + 35330945 35330945 35330945 CATTTTTAGTTTATTTTTTATCTTTTTGAGACAGGGTCTTGCCCTGTCGCCCAGGCTGGAGTGCA CATTTTTAGTTTATTTTTTATCTTTTTGAGACCGGGTCTTGCCCTGTCGCCCAGGCTGGAGTGCA A C CD22,U62631.1 Ensembl:ENSG00000012124,Ensembl:ENSG00000269553 Protein coding,lincRNA intron,exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs567487210 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6800527 26298 RMVar_ID_26298 Human_SNP_ID_664452281 A-to-I Human chr19 + 35330983 35330983 35330983 TTGCCCTGTCGCCCAGGCTGGAGTGCAGTTGCATGATCTCGGCTCATTCCAACTTCTACTTCCCG TTGCCCTGTCGCCCAGGCTGGAGTGCAGTTGCGTGATCTCGGCTCATTCCAACTTCTACTTCCCG A G CD22,U62631.1 Ensembl:ENSG00000012124,Ensembl:ENSG00000269553 Protein coding,lincRNA intron,exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs373569928 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1993493 26299 RMVar_ID_26299 Human_SNP_ID_664452289 A-to-I Human chr19 + 35331008 35331008 35331008 CAGTTGCATGATCTCGGCTCATTCCAACTTCTACTTCCCGGGTTCAAGCAATTCTCCTGCCTCAG CAGTTGCATGATCTCGGCTCATTCCAACTTCTGCTTCCCGGGTTCAAGCAATTCTCCTGCCTCAG A G CD22,U62631.1 Ensembl:ENSG00000012124,Ensembl:ENSG00000269553 Protein coding,lincRNA intron,exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1445077907 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1993493 26300 RMVar_ID_26300 Human_SNP_ID_664452315 A-to-I Human chr19 + 35331087 35331087 35331087 GGGATTACAGGTGTACGCCACCACGCCTGGCTAATTTTTTGCATTTTGAGTAAAGATGGGGTTTT GGGATTACAGGTGTACGCCACCACGCCTGGCTGATTTTTTGCATTTTGAGTAAAGATGGGGTTTT A G CD22,U62631.1 Ensembl:ENSG00000012124,Ensembl:ENSG00000269553 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1270741192 Functional Loss SNV dbSNP153 33..33 33 - - - 26301 RMVar_ID_26301 Human_SNP_ID_664452454 A-to-I Human chr19 + 35331754 35331754 35331754 GCCTTTACCCAGCTACTTGGGGGGCTGAGGCCAGAGAAACGCTTGAGCCTGGGAAGCAGAGGTTG GCCTTTACCCAGCTACTTGGGGGGCTGAGGCCGGAGAAACGCTTGAGCCTGGGAAGCAGAGGTTG A G CD22,U62631.1 Ensembl:ENSG00000012124,Ensembl:ENSG00000269553 Protein coding,lincRNA intron,exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs865779051 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1993494 26302 RMVar_ID_26302 Human_SNP_ID_664452458 A-to-I Human chr19 + 35331779 35331779 35331779 TGAGGCCAGAGAAACGCTTGAGCCTGGGAAGCAGAGGTTGCAGTGAGCGGAGATCACACCACTGC TGAGGCCAGAGAAACGCTTGAGCCTGGGAAGCTGAGGTTGCAGTGAGCGGAGATCACACCACTGC A T CD22,U62631.1 Ensembl:ENSG00000012124,Ensembl:ENSG00000269553 Protein coding,lincRNA intron,exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1050437230 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1993494 26303 RMVar_ID_26303 Human_SNP_ID_664452903 A-to-I Human chr19 + 35333279 35333279 35333279 AGCACCGCATTCCTTTAGTGGGGTGGGTCTGCATGTAACCAGCCTCAGCTCTCCCCCAGGCTGGA AGCACCGCATTCCTTTAGTGGGGTGGGTCTGCGTGTAACCAGCCTCAGCTCTCCCCCAGGCTGGA A G CD22 Ensembl:ENSG00000012124 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1472508062 Functional Loss SNV dbSNP153 33..33 33 - - - 26304 RMVar_ID_26304 Human_SNP_ID_664452937 A-to-I Human chr19 + 35333411 35333411 35333411 CCCTATAGAGGAAACTGGGTGTGGAACGGAGTAACCACACTCCCTAGGGCAGAGGCCCCAGACCT CCCTATAGAGGAAACTGGGTGTGGAACGGAGTGACCACACTCCCTAGGGCAGAGGCCCCAGACCT A G CD22 Ensembl:ENSG00000012124 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1446629933 Functional Loss SNV dbSNP153 33..33 33 - - - 26305 RMVar_ID_26305 Human_SNP_ID_664453187 A-to-I Human chr19 + 35334516 35334516 35334516 CATCAAACACAGGTGTGGGGGGCCCCTGCCACAGGGAGTGTGGTCACTCCGTTCCACACCGTTTC CATCAAACACAGGTGTGGGGGGCCCCTGCCACGGGGAGTGTGGTCACTCCGTTCCACACCGTTTC A G CD22 Ensembl:ENSG00000012124 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1050957069 Functional Loss SNV dbSNP153 33..33 33 - - - 26306 RMVar_ID_26306 Human_SNP_ID_664453211 A-to-I Human chr19 + 35334629 35334629 35334629 CTTCAGACCCCGCTGTCTGAAGGAGGTGGTCCAGCCTTGGGGAGAGCTGAGGCTGGGTGCACACA CTTCAGACCCCGCTGTCTGAAGGAGGTGGTCCGGCCTTGGGGAGAGCTGAGGCTGGGTGCACACA A G CD22 Ensembl:ENSG00000012124 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs545646812 Functional Loss SNV dbSNP153 33..33 33 - - - 26307 RMVar_ID_26307 Human_SNP_ID_664455699 A-to-I Human chr19 + 35342335 35342335 35342335 GGGACTATAGACATGCACCACCACATCCGGCTAATTTTTACATTTTTGTAGAGATGGGGTCTTAC GGGACTATAGACATGCACCACCACATCCGGCTTATTTTTACATTTTTGTAGAGATGGGGTCTTAC A T CD22 Ensembl:ENSG00000012124 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1276825053 Functional Loss SNV dbSNP153 33..33 33 - - - 26308 RMVar_ID_26308 Human_SNP_ID_664475081 A-to-I Human chr19 + 35413378 35413368 35413378 CATCAACCTCAGCCTCTCAAAGTGCTAGAATTACAGGTTTGAGCCACCGCGCCTGGCCTAAGGAT CATCAACCTCAGCCTCTCAAAGT__________CAGGTTTGAGCCACCGCGCCTGGCCTAAGGAT TGCTAGAATTA T LINC01531 Ensembl:ENSG00000205786 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1568512208 Functional Loss DEL dbSNP153 24..33 33 - - - 26309 RMVar_ID_26309 Human_SNP_ID_664475084 A-to-I Human chr19 + 35413378 35413369 35413378 CATCAACCTCAGCCTCTCAAAGTGCTAGAATTACAGGTTTGAGCCACCGCGCCTGGCCTAAGGAT CATCAACCTCAGCCTCTCAAAGTG_________CAGGTTTGAGCCACCGCGCCTGGCCTAAGGAT GCTAGAATTA G LINC01531 Ensembl:ENSG00000205786 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs769432446 Functional Loss DEL dbSNP153 25..33 33 - - - 26310 RMVar_ID_26310 Human_SNP_ID_664475086 A-to-I Human chr19 + 35413378 35413378 35413378 CATCAACCTCAGCCTCTCAAAGTGCTAGAATTACAGGTTTGAGCCACCGCGCCTGGCCTAAGGAT CATCAACCTCAGCCTCTCAAAGTGCTAGAATTGCAGGTTTGAGCCACCGCGCCTGGCCTAAGGAT A G LINC01531 Ensembl:ENSG00000205786 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904564492 Functional Loss SNV dbSNP153 33..33 33 - - - 26311 RMVar_ID_26311 Human_SNP_ID_664499467 A-to-I Human chr19 - 35506822 35506822 35506822 TTTAGTAGAGATGGGGTTTCACTATGTTGGCCAGGCTGTTTTCAAACTCCTGACCTCAGGTGATC TTTAGTAGAGATGGGGTTTCACTATGTTGGCCGGGCTGTTTTCAAACTCCTGACCTCAGGTGATC T C DMKN Ensembl:ENSG00000161249 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1427646497 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110986,RMVar_hsa_circ_194230,RMVar_hsa_circ_377738 26312 RMVar_ID_26312 Human_SNP_ID_664500370 A-to-I Human chr19 - 35510325 35510325 35510325 CTGGAATCTGATTGGGGTTCCAACAAATCTGTAACACCGCTGGGAACGACTGGGTCCCCTTTAGG CTGGAATCTGATTGGGGTTCCAACAAATCTGTGACACCGCTGGGAACGACTGGGTCCCCTTTAGG T C DMKN Ensembl:ENSG00000161249 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1230626661 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1560983,Human_RBP_ID_8484320,Human_RBP_ID_18729020,Human_RBP_ID_22546773,Human_RBP_ID_22970494,Human_RBP_ID_25444571 26313 RMVar_ID_26313 Human_SNP_ID_664518922 A-to-I Human chr19 + 35575675 35575675 35575675 CAGCAGGACGGTGGCCATGGAAGTCAGAATCCACTAAGGAGTGTGTAACAACTCACCTGCCGAAT CAGCAGGACGGTGGCCATGGAAGTCAGAATCCGCTAAGGAGTGTGTAACAACTCACCTGCCGAAT A G AD000090.1 Ensembl:ENSG00000283907 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs79755095 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_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 26314 RMVar_ID_26314 Human_SNP_ID_664518939 A-to-I Human chr19 + 35575740 35575740 35575740 CAACTAGCCCTGAAAATGGATGGCACTGGAGCATCAGGCCCATACCCGGCCATCGCCAGCAGTCA CAACTAGCCCTGAAAATGGATGGCACTGGAGCGTCAGGCCCATACCCGGCCATCGCCAGCAGTCA A G AD000090.1 Ensembl:ENSG00000283907 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs62109966 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_270101,Human_RBP_ID_1064019,Human_RBP_ID_4521098,Human_RBP_ID_5190631,Human_RBP_ID_5443005,Human_RBP_ID_5468659,Human_RBP_ID_5499419,Human_RBP_ID_6803196,Human_RBP_ID_8096729,Human_RBP_ID_8255988,Human_RBP_ID_8840581,Human_RBP_ID_9086863,Human_RBP_ID_9258621,Human_RBP_ID_9291857,Human_RBP_ID_13548737,Human_RBP_ID_17011164,Human_RBP_ID_17063375,Human_RBP_ID_17268045,Human_RBP_ID_17695346,Human_RBP_ID_17936269,Human_RBP_ID_18200692,Human_RBP_ID_18208633,Human_RBP_ID_18441102,Human_RBP_ID_18514858,Human_RBP_ID_20380048,Human_RBP_ID_21929851,Human_RBP_ID_22233974,Human_RBP_ID_22422486,Human_RBP_ID_22502420,Human_RBP_ID_22810494,Human_RBP_ID_23176346,Human_RBP_ID_23279576,Human_RBP_ID_23309543,Human_RBP_ID_23793567,Human_RBP_ID_26467462,Human_RBP_ID_26652666,Human_RBP_ID_26749474,Human_RBP_ID_26988693,Human_RBP_ID_27157562,Human_RBP_ID_27280890,Human_RBP_ID_27473449,Human_RBP_ID_27562410,Human_RBP_ID_27677532 26315 RMVar_ID_26315 Human_SNP_ID_664518941 A-to-I Human chr19 + 35575743 35575743 35575743 CTAGCCCTGAAAATGGATGGCACTGGAGCATCAGGCCCATACCCGGCCATCGCCAGCAGTCAATG CTAGCCCTGAAAATGGATGGCACTGGAGCATCGGGCCCATACCCGGCCATCGCCAGCAGTCAATG A G AD000090.1 Ensembl:ENSG00000283907 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs62109967 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_270101,Human_RBP_ID_1064019,Human_RBP_ID_4521098,Human_RBP_ID_5190632,Human_RBP_ID_5443005,Human_RBP_ID_5468659,Human_RBP_ID_5499419,Human_RBP_ID_6803196,Human_RBP_ID_8096729,Human_RBP_ID_8255988,Human_RBP_ID_8840581,Human_RBP_ID_9086863,Human_RBP_ID_9258621,Human_RBP_ID_9291857,Human_RBP_ID_13548737,Human_RBP_ID_17011164,Human_RBP_ID_17063375,Human_RBP_ID_17268045,Human_RBP_ID_17695346,Human_RBP_ID_17936269,Human_RBP_ID_18200692,Human_RBP_ID_18208633,Human_RBP_ID_18441102,Human_RBP_ID_18514858,Human_RBP_ID_20380048,Human_RBP_ID_21929851,Human_RBP_ID_22233974,Human_RBP_ID_22422486,Human_RBP_ID_22502420,Human_RBP_ID_22810494,Human_RBP_ID_23176346,Human_RBP_ID_23279576,Human_RBP_ID_23309543,Human_RBP_ID_23793567,Human_RBP_ID_26474837,Human_RBP_ID_26652666,Human_RBP_ID_26749474,Human_RBP_ID_26988693,Human_RBP_ID_27157562,Human_RBP_ID_27280890,Human_RBP_ID_27473449,Human_RBP_ID_27562410,Human_RBP_ID_27677532 26316 RMVar_ID_26316 Human_SNP_ID_664518948 A-to-I Human chr19 + 35575759 35575759 35575759 ATGGCACTGGAGCATCAGGCCCATACCCGGCCATCGCCAGCAGTCAATGGAATGTGAGTGCCTTA ATGGCACTGGAGCATCAGGCCCATACCCGGCCGTCGCCAGCAGTCAATGGAATGTGAGTGCCTTA A G AD000090.1 Ensembl:ENSG00000283907 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs79083609 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_270008,Human_RBP_ID_1064019,Human_RBP_ID_5194225,Human_RBP_ID_8103461,Human_RBP_ID_26467463 26317 RMVar_ID_26317 Human_SNP_ID_664518952 A-to-I Human chr19 + 35575765 35575765 35575765 CTGGAGCATCAGGCCCATACCCGGCCATCGCCAGCAGTCAATGGAATGTGAGTGCCTTAGAGGTC CTGGAGCATCAGGCCCATACCCGGCCATCGCCGGCAGTCAATGGAATGTGAGTGCCTTAGAGGTC A G AD000090.1 Ensembl:ENSG00000283907 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs79382536 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_270008,Human_RBP_ID_1064019,Human_RBP_ID_5194225,Human_RBP_ID_8103461,Human_RBP_ID_26467463 26318 RMVar_ID_26318 Human_SNP_ID_664528976 A-to-I Human chr19 + 35616171 35616171 35616171 AAACCCCGTCCCTACTAAAAAATACAAAAATTAGTCGAGTGTGGTGGCACGTGCCTGTAGTCCCA AAACCCCGTCCCTACTAAAAAATACAAAAATTTGTCGAGTGTGGTGGCACGTGCCTGTAGTCCCA A T HAUS5 Ensembl:ENSG00000249115 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1391040410 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92706,RMVar_hsa_circ_95661,RMVar_hsa_circ_194245,RMVar_hsa_circ_194246 26319 RMVar_ID_26319 Human_SNP_ID_664538579 A-to-I Human chr19 + 35650238 35650238 35650238 GTTGGCCAGGCTGGTCTTGAACTCCTGACCTCAGGTGATCCACCCCCCTGGCCTCCCAAAGTGCT GTTGGCCAGGCTGGTCTTGAACTCCTGACCTCGGGTGATCCACCCCCCTGGCCTCCCAAAGTGCT A G COX6B1 Ensembl:ENSG00000126267 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928576365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13436625 RMVar_hsa_circ_125126,RMVar_hsa_circ_194257 26320 RMVar_ID_26320 Human_SNP_ID_664573012 A-to-I Human chr19 + 35762447 35762447 35762447 ACAGAATTAGAAGATCAGGAGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGT ACAGAATTAGAAGATCAGGAGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGT A G PROSER3 Ensembl:ENSG00000167595 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1448291928 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13437073 Human_Splice_Rec_1996107 RMVar_hsa_circ_101237,RMVar_hsa_circ_371688,RMVar_hsa_circ_123286,RMVar_hsa_circ_194284,RMVar_hsa_circ_194285,RMVar_hsa_circ_194286 26321 RMVar_ID_26321 Human_SNP_ID_664573071 A-to-I Human chr19 + 35762681 35762681 35762681 CTAGGAGTTCAAGGCTGCTGTGAGCTATGATCATGCCACTGCACTCCAGCCTGGGCAGTAGAGCA CTAGGAGTTCAAGGCTGCTGTGAGCTATGATCGTGCCACTGCACTCCAGCCTGGGCAGTAGAGCA A G PROSER3 Ensembl:ENSG00000167595 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1365485277 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22979000 RMVar_hsa_circ_101237,RMVar_hsa_circ_371688,RMVar_hsa_circ_123286,RMVar_hsa_circ_194284,RMVar_hsa_circ_194285,RMVar_hsa_circ_194286 26322 RMVar_ID_26322 Human_SNP_ID_664573108 A-to-I Human chr19 + 35762778 35762778 35762778 AAAAAAGCCTGGGCACCGTGGCTCATGCCTATAATCCCAGCACTTTGGTAGGCTGAGGCAGGCAG AAAAAAGCCTGGGCACCGTGGCTCATGCCTATGATCCCAGCACTTTGGTAGGCTGAGGCAGGCAG A G PROSER3 Ensembl:ENSG00000167595 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1212510647 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101237,RMVar_hsa_circ_371688,RMVar_hsa_circ_123286,RMVar_hsa_circ_194284,RMVar_hsa_circ_194285,RMVar_hsa_circ_194286 26323 RMVar_ID_26323 Human_SNP_ID_664573148 A-to-I Human chr19 + 35762986 35762986 35762986 CCCGGGAGACGGAGGTTGCAGTGAGCCAAGATAGCGCCAGCGCACTCCAGCCTGGCGACAGCAAG CCCGGGAGACGGAGGTTGCAGTGAGCCAAGATGGCGCCAGCGCACTCCAGCCTGGCGACAGCAAG A G PROSER3 Ensembl:ENSG00000167595 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs922374152 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9917078,Human_RBP_ID_13437077,Human_RBP_ID_22970718,Human_RBP_ID_25444638 RMVar_hsa_circ_101237,RMVar_hsa_circ_371688,RMVar_hsa_circ_123286,RMVar_hsa_circ_194284,RMVar_hsa_circ_194285,RMVar_hsa_circ_194286 26324 RMVar_ID_26324 Human_SNP_ID_664573458 A-to-I Human chr19 + 35763948 35763948 35763948 TACCTGGGACTACAGCATGCGCCACCATGCCCAGCTAATTTTTTGGTTTTTTTGTAGAGATGGGA TACCTGGGACTACAGCATGCGCCACCATGCCCGGCTAATTTTTTGGTTTTTTTGTAGAGATGGGA A G PROSER3 Ensembl:ENSG00000167595 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1568411064 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23176378 RMVar_hsa_circ_371688,RMVar_hsa_circ_123286,RMVar_hsa_circ_194285,RMVar_hsa_circ_194286 26325 RMVar_ID_26325 Human_SNP_ID_664575456 A-to-I Human chr19 + 35770107 35770107 35770107 TTGTATTTTTAGTAGAGACGGGGTTTCACCATATTGGCCAGGCTGGTCTCAAACTCATGACCTCG TTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTCATGACCTCG A G PROSER3 Ensembl:ENSG00000167595 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs911471640 Functional Loss SNV dbSNP153 33..33 33 - - - 26326 RMVar_ID_26326 Human_SNP_ID_664575474 A-to-I Human chr19 + 35770164 35770164 35770164 TGACCTCGTGATCCTCCTGCCTCAGCCTCCCAAAGCGCTGGGATTACAGGCATGAGCCATCATGC TGACCTCGTGATCCTCCTGCCTCAGCCTCCCATAGCGCTGGGATTACAGGCATGAGCCATCATGC A T PROSER3 Ensembl:ENSG00000167595 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042817873 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23176400 26327 RMVar_ID_26327 Human_SNP_ID_664575511 A-to-I Human chr19 + 35770306 35770306 35770306 GTGTCCCACCCACCTCAGCCTCCCAAAGTGCTAGGATTACAGATGTGAGCCACCGCACCTGGCCT GTGTCCCACCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGATGTGAGCCACCGCACCTGGCCT A G PROSER3 Ensembl:ENSG00000167595 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229,31158229 RNA-Seq:(High) rs944071687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23176403 26328 RMVar_ID_26328 Human_SNP_ID_664575577 A-to-I Human chr19 + 35770604 35770604 35770604 TGCAGTTAGAAAAGATGATTTCTCAGCTGGGCATGGTGGCTCACGCCTGTAATCCCAGCACTTTG TGCAGTTAGAAAAGATGATTTCTCAGCTGGGCGTGGTGGCTCACGCCTGTAATCCCAGCACTTTG A G PROSER3 Ensembl:ENSG00000167595 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1266595959 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17383232 26329 RMVar_ID_26329 Human_SNP_ID_664575584 A-to-I Human chr19 + 35770653 35770653 35770653 TAATCCCAGCACTTTGGGAGGCTCAGGTGGGCAGATTACTTGAGGTCAGGGGTTCAAGACCAGCC TAATCCCAGCACTTTGGGAGGCTCAGGTGGGCGGATTACTTGAGGTCAGGGGTTCAAGACCAGCC A G PROSER3 Ensembl:ENSG00000167595 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1324132593 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13437261 26330 RMVar_ID_26330 Human_SNP_ID_664575586 A-to-I Human chr19 + 35770663 35770663 35770663 ACTTTGGGAGGCTCAGGTGGGCAGATTACTTGAGGTCAGGGGTTCAAGACCAGCCTGGCCAACAT ACTTTGGGAGGCTCAGGTGGGCAGATTACTTGTGGTCAGGGGTTCAAGACCAGCCTGGCCAACAT A T PROSER3 Ensembl:ENSG00000167595 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs554028729 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13437261 26331 RMVar_ID_26331 Human_SNP_ID_664575601 A-to-I Human chr19 + 35770719 35770719 35770719 GGCCAACATGGTGAAATGTCTCTACTAAAAATACAAAAATTGGCCAGGCATTGGTGGTGGGTGCC GGCCAACATGGTGAAATGTCTCTACTAAAAATCCAAAAATTGGCCAGGCATTGGTGGTGGGTGCC A C PROSER3 Ensembl:ENSG00000167595 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs990702448 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25405606 26332 RMVar_ID_26332 Human_SNP_ID_664575602 A-to-I Human chr19 + 35770719 35770719 35770719 GGCCAACATGGTGAAATGTCTCTACTAAAAATACAAAAATTGGCCAGGCATTGGTGGTGGGTGCC GGCCAACATGGTGAAATGTCTCTACTAAAAATGCAAAAATTGGCCAGGCATTGGTGGTGGGTGCC A G PROSER3 Ensembl:ENSG00000167595 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs990702448 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25405606 26333 RMVar_ID_26333 Human_SNP_ID_664575620 A-to-I Human chr19 + 35770801 35770801 35770801 AGGAGGCTGAGGCAAGAGAATTGCTTGAACTCAGAAGGCAGAGGTTGCAGTGGAAAAAAAAAAAA AGGAGGCTGAGGCAAGAGAATTGCTTGAACTCGGAAGGCAGAGGTTGCAGTGGAAAAAAAAAAAA A G PROSER3 Ensembl:ENSG00000167595 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs548454803 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6747066,Human_RBP_ID_25405608 26334 RMVar_ID_26334 Human_SNP_ID_664611435 A-to-I Human chr19 - 35891755 35891755 35891755 TCAAGCTATTCCTGTGTCTCAGCCTCCCAAGTAGCTGGGATTATAGGCATGTGCCACCACGCCTG TCAAGCTATTCCTGTGTCTCAGCCTCCCAAGTGGCTGGGATTATAGGCATGTGCCACCACGCCTG T C NFKBID Ensembl:ENSG00000167604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1169795148 Functional Loss SNV dbSNP153 33..33 33 - - - 26335 RMVar_ID_26335 Human_SNP_ID_664611437 A-to-I Human chr19 - 35891767 35891767 35891767 TGCCTCCCGGGTTCAAGCTATTCCTGTGTCTCAGCCTCCCAAGTAGCTGGGATTATAGGCATGTG TGCCTCCCGGGTTCAAGCTATTCCTGTGTCTCGGCCTCCCAAGTAGCTGGGATTATAGGCATGTG T C NFKBID Ensembl:ENSG00000167604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs557676732 Functional Loss SNV dbSNP153 33..33 33 - - - 26336 RMVar_ID_26336 Human_SNP_ID_664611454 A-to-I Human chr19 - 35891828 35891828 35891828 GAGTCTCACTCTGTTGCCCAGGCTGGATTGCAATGGTGTGATTTTGGCTCACTGCAACCTCTGCC GAGTCTCACTCTGTTGCCCAGGCTGGATTGCAGTGGTGTGATTTTGGCTCACTGCAACCTCTGCC T C NFKBID Ensembl:ENSG00000167604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1308967667 Functional Loss SNV dbSNP153 33..33 33 - - - 26337 RMVar_ID_26337 Human_SNP_ID_664611455 A-to-I Human chr19 - 35891828 35891828 35891828 GAGTCTCACTCTGTTGCCCAGGCTGGATTGCAATGGTGTGATTTTGGCTCACTGCAACCTCTGCC GAGTCTCACTCTGTTGCCCAGGCTGGATTGCACTGGTGTGATTTTGGCTCACTGCAACCTCTGCC T G NFKBID Ensembl:ENSG00000167604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1308967667 Functional Loss SNV dbSNP153 33..33 33 - - - 26338 RMVar_ID_26338 Human_SNP_ID_664611551 A-to-I Human chr19 - 35892198 35892198 35892198 AAAATACAAAAATTAGCTGGGCTTGATGGCACATGCCTGTGGTCCCAGGTACTCAGGAGGCTGAG AAAATACAAAAATTAGCTGGGCTTGATGGCACGTGCCTGTGGTCCCAGGTACTCAGGAGGCTGAG T C NFKBID Ensembl:ENSG00000167604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1253570741 Functional Loss SNV dbSNP153 33..33 33 - - - 26339 RMVar_ID_26339 Human_SNP_ID_664611576 A-to-I Human chr19 - 35892279 35892279 35892279 GGGAGGCTCAGGTGGGCGGACTGCTCGAGCTCAGGAATTCGAGACCAACCTGGGCAACATAGGGA GGGAGGCTCAGGTGGGCGGACTGCTCGAGCTCCGGAATTCGAGACCAACCTGGGCAACATAGGGA T G NFKBID Ensembl:ENSG00000167604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1256032619 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5443018 26340 RMVar_ID_26340 Human_SNP_ID_664611617 A-to-I Human chr19 - 35892450 35892450 35892450 AACCTCCCAGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTATAGGCATGTG AACCTCCCAGGTTCAAGTGATTCTCCTGCCTCTGCCTCCCGAGTAGCTGGGACTATAGGCATGTG T A NFKBID Ensembl:ENSG00000167604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1025525660 Functional Loss SNV dbSNP153 33..33 33 - - - 26341 RMVar_ID_26341 Human_SNP_ID_664611626 A-to-I Human chr19 - 35892506 35892506 35892506 GGAGTCTCGCTCTGTCGCCCAGGTTGGAGTGCAGTGGCACAGTCTTGGTTCACTGCAACCTCCCA GGAGTCTCGCTCTGTCGCCCAGGTTGGAGTGCCGTGGCACAGTCTTGGTTCACTGCAACCTCCCA T G NFKBID Ensembl:ENSG00000167604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs138110997 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_96 26342 RMVar_ID_26342 Human_SNP_ID_664613618 A-to-I Human chr19 + 35899405 35899405 35899405 TGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATATAAAAATTAGCCGGGCGTGGTGGCAGGC TGGCCAACATGGTGAAACCCCGTCTCTACTAAGAATATAAAAATTAGCCGGGCGTGGTGGCAGGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1273418131 Functional Loss SNV dbSNP153 33..33 33 - - - 26343 RMVar_ID_26343 Human_SNP_ID_664627115 A-to-I Human chr19 + 35948202 35948202 35948202 GGCATGTGCCACCACACCCAGCTAATTTTTGTATTTTTGTAGAGATGGGGGTCTCACTGTGTTCC GGCATGTGCCACCACACCCAGCTAATTTTTGTGTTTTTGTAGAGATGGGGGTCTCACTGTGTTCC A G AF038458.3 Ensembl:ENSG00000267786 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1305465883 Functional Loss SNV dbSNP153 33..33 33 - - - 26344 RMVar_ID_26344 Human_SNP_ID_664630233 A-to-I Human chr19 + 35960485 35960485 35960485 AATTTTTGTATTTTTACTAGAGACTGGGTATCAGCATGTTGGCCAGGCTGGTCTTGAGCTCCTGA AATTTTTGTATTTTTACTAGAGACTGGGTATCGGCATGTTGGCCAGGCTGGTCTTGAGCTCCTGA A G LOC105372383 RNACentral:URS0000A76FDF lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1353672851 Functional Loss SNV dbSNP153 33..33 33 - - - 26345 RMVar_ID_26345 Human_SNP_ID_664646086 A-to-I Human chr19 + 36020345 36020345 36020345 TAAATTTAGTCCGGGCGCGGTGGCTCACACCTATAATCCTAGCACTCTGGGAGGCCGAGGTGGGA TAAATTTAGTCCGGGCGCGGTGGCTCACACCTGTAATCCTAGCACTCTGGGAGGCCGAGGTGGGA A G AC002116.2 Ensembl:ENSG00000267698 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs550350105 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3588934,Human_RBP_ID_25405837 26346 RMVar_ID_26346 Human_SNP_ID_664646244 A-to-I Human chr19 + 36021098 36021098 36021098 TGGAGTATCCCTATGTTGCCCAGGTTAGTTTCAAACTCCTGGCCTCAAGCGATCCTCCCCATCTT TGGAGTATCCCTATGTTGCCCAGGTTAGTTTCTAACTCCTGGCCTCAAGCGATCCTCCCCATCTT A T AC002116.2 Ensembl:ENSG00000267698 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs951902274 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5248708 26347 RMVar_ID_26347 Human_SNP_ID_664646498 A-to-I Human chr19 + 36022252 36022252 36022252 ACAGTGCCTGGCACACACAAAGAGCATTTAGTATGCGCTGGACTCTGTTCTAATGGCCTTACGCA ACAGTGCCTGGCACACACAAAGAGCATTTAGTGTGCGCTGGACTCTGTTCTAATGGCCTTACGCA A G AC002116.2 Ensembl:ENSG00000267698 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749335900 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13437699 26348 RMVar_ID_26348 Human_SNP_ID_664652194 A-to-I Human chr19 + 36043111 36043111 36043111 CCACTGCACCTGGCTATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGG CCACTGCACCTGGCTATTTTTGTATTTTTAGTGGAGATGGGGTTTCACCATGTTGGCCAGGCTGG A G AC002116.2 Ensembl:ENSG00000267698 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1329361280 Functional Loss SNV dbSNP153 33..33 33 - - - 26349 RMVar_ID_26349 Human_SNP_ID_664652549 A-to-I Human chr19 + 36044690 36044690 36044690 TTAAAATTTCTTTTTGTAGAGACAGAGGTCTCACTATGTTGTCCAGACTGGTCTTGAACTCCTGG TTAAAATTTCTTTTTGTAGAGACAGAGGTCTCGCTATGTTGTCCAGACTGGTCTTGAACTCCTGG A G AC002116.2 Ensembl:ENSG00000267698 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1392397992 Functional Loss SNV dbSNP153 33..33 33 - - - 26350 RMVar_ID_26350 Human_SNP_ID_664657226 A-to-I Human chr19 + 36062155 36062154 36062155 TTTTAGTGGAGACGGGGTTCATCATGTTGCCCAAGGTGGTCTTGAACTCCTGAGCTTAGACAGTC TTTTAGTGGAGACGGGGTTCATCATGTTGCCC_AGGTGGTCTTGAACTCCTGAGCTTAGACAGTC CA C WDR62 Ensembl:ENSG00000075702 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1424775895 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_13438037 RMVar_hsa_circ_76663,RMVar_hsa_circ_94904,RMVar_hsa_circ_194315,RMVar_hsa_circ_78063,RMVar_hsa_circ_194314,RMVar_hsa_circ_82432,RMVar_hsa_circ_194316,RMVar_hsa_circ_341567,RMVar_hsa_circ_194317,RMVar_hsa_circ_194318 26351 RMVar_ID_26351 Human_SNP_ID_664661254 A-to-I Human chr19 + 36075164 36075163 36075164 TCAAGTGATTCTCCTGCCTCGGCCTCTCAGGTAGCTGGGATTCCAGGCATGCGCCACCACGCCTT TCAAGTGATTCTCCTGCCTCGGCCTCTCAGGT_GCTGGGATTCCAGGCATGCGCCACCACGCCTT TA T WDR62 Ensembl:ENSG00000075702 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1177366718 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_76663,RMVar_hsa_circ_94904,RMVar_hsa_circ_194315,RMVar_hsa_circ_78063,RMVar_hsa_circ_194314,RMVar_hsa_circ_95975,RMVar_hsa_circ_82432,RMVar_hsa_circ_194316,RMVar_hsa_circ_194318,RMVar_hsa_circ_87630,RMVar_hsa_circ_194323,RMVar_hsa_circ_118547,RMVar_hsa_circ_104178,RMVar_hsa_circ_120943,RMVar_hsa_circ_194324,RMVar_hsa_circ_194325,RMVar_hsa_circ_375874,RMVar_hsa_circ_194328,RMVar_hsa_circ_100446,RMVar_hsa_circ_194330,RMVar_hsa_circ_194331,RMVar_hsa_circ_194329 26352 RMVar_ID_26352 Human_SNP_ID_664673717 A-to-I Human chr19 + 36116863 36116863 36116863 GGCTGGTCTGGAACTCCTGACCTCAAGTGATCAGCTCACCTTGGCCTACTAAAGTGCTGGGATTA GGCTGGTCTGGAACTCCTGACCTCAAGTGATCGGCTCACCTTGGCCTACTAAAGTGCTGGGATTA A G TBCB Ensembl:ENSG00000105254 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs957285545 Functional Loss SNV dbSNP153 33..33 33 - - - 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 26353 RMVar_ID_26353 Human_SNP_ID_664674440 A-to-I Human chr19 + 36119610 36119610 36119610 CTTCGCTCCAGATAAAAACCAAAGTCTAGGCCAGGTGCGGTGGATCGTGCCTGTAATCCCACCCA CTTCGCTCCAGATAAAAACCAAAGTCTAGGCCGGGTGCGGTGGATCGTGCCTGTAATCCCACCCA A G TBCB Ensembl:ENSG00000105254 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973439077 Functional Loss SNV dbSNP153 33..33 33 - - - 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 26354 RMVar_ID_26354 Human_SNP_ID_664674474 A-to-I Human chr19 + 36119770 36119770 36119770 CAAAAATTAGCCGGGTGTGGTGGTGTGTGCCTATAGTTTCAGCTGCCCGGGAGGCTGAGGCAGGA CAAAAATTAGCCGGGTGTGGTGGTGTGTGCCTGTAGTTTCAGCTGCCCGGGAGGCTGAGGCAGGA A G TBCB Ensembl:ENSG00000105254 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1034787616 Functional Loss SNV dbSNP153 33..33 33 - - - 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 26355 RMVar_ID_26355 Human_SNP_ID_664674476 A-to-I Human chr19 + 36119772 36119772 36119772 AAAATTAGCCGGGTGTGGTGGTGTGTGCCTATAGTTTCAGCTGCCCGGGAGGCTGAGGCAGGAGA AAAATTAGCCGGGTGTGGTGGTGTGTGCCTATGGTTTCAGCTGCCCGGGAGGCTGAGGCAGGAGA A G TBCB Ensembl:ENSG00000105254 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1330997276 Functional Loss SNV dbSNP153 33..33 33 - - - 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 26356 RMVar_ID_26356 Human_SNP_ID_664675758 A-to-I Human chr19 + 36123464 36123464 36123464 TTGTGGTTTTTTTTGTAGGATGGGATTTCGCCATGTGGCCCAGGCTGGTCTCAAACTCTTCCCGC TTGTGGTTTTTTTTGTAGGATGGGATTTCGCCGTGTGGCCCAGGCTGGTCTCAAACTCTTCCCGC A G TBCB Ensembl:ENSG00000105254 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs369595160 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 26357 RMVar_ID_26357 Human_SNP_ID_664681710 A-to-I Human chr19 + 36145304 36145304 36145304 TTGGCTCACTGCTAACTCCACCTCCTAGGTTCAAGCAGTTCTCCTCCCTCAGCCTCCTGAATAGC TTGGCTCACTGCTAACTCCACCTCCTAGGTTCGAGCAGTTCTCCTCCCTCAGCCTCCTGAATAGC A G CAPNS1 Ensembl:ENSG00000126247 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1022265550 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 26358 RMVar_ID_26358 Human_SNP_ID_664700728 A-to-I Human chr19 - 36213253 36213253 36213253 TGAGCCGTGTTTGAACCACTGCATTCCAGTCTAGGTGACAGAGCGAGACCCTGTCTCAAAAAAAT TGAGCCGTGTTTGAACCACTGCATTCCAGTCTCGGTGACAGAGCGAGACCCTGTCTCAAAAAAAT T G ZNF565 Ensembl:ENSG00000196357 Protein coding intron GSE100210;GSE105773 HepG2 cell line;Glioblastoma cells,U87MG - 29129909,29724793 RNA-Seq:(High) rs1398255343 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1998201 26359 RMVar_ID_26359 Human_SNP_ID_664701881 A-to-I Human chr19 + 36217111 36217111 36217111 TTGAGATGGAGTCTCTCTCTCTTGCCCAGTCTAGAGTGCAGTGGCCCAATCTCTGCTCCCTGCAA TTGAGATGGAGTCTCTCTCTCTTGCCCAGTCTGGAGTGCAGTGGCCCAATCTCTGCTCCCTGCAA A G ZNF146 Ensembl:ENSG00000167635 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1240725680 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13439052 26360 RMVar_ID_26360 Human_SNP_ID_664701912 A-to-I Human chr19 + 36217243 36217243 36217243 CCACCACACCCGGCTACTTTTTTTGTATTTTTAGTAGAGACAGGGTTTTACCATGTTGGCCAGGC CCACCACACCCGGCTACTTTTTTTGTATTTTTGGTAGAGACAGGGTTTTACCATGTTGGCCAGGC A G ZNF146 Ensembl:ENSG00000167635 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1217016875 Functional Loss SNV dbSNP153 33..33 33 - - - 26361 RMVar_ID_26361 Human_SNP_ID_664701928 A-to-I Human chr19 + 36217297 36217296 36217297 GTTGGCCAGGCTGGTCTTGAACTCTTGACCTCAAGTGATCGGCCCGCCTCGGCTTCCCAAAGTGC GTTGGCCAGGCTGGTCTTGAACTCTTGACCTC_AGTGATCGGCCCGCCTCGGCTTCCCAAAGTGC CA C ZNF146 Ensembl:ENSG00000167635 Protein coding intron GSE38233;GSE100210;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,frontal_cortex - 24183664,29129909,30559470 RNA-Seq:(High) rs1167751920 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_6747870,Human_RBP_ID_13439054 26362 RMVar_ID_26362 Human_SNP_ID_664702003 A-to-I Human chr19 + 36217656 36217656 36217656 TTTATAATCCCAGCACTTTGGGAGGCCAACGCAGGCGGATCACCTGAGGTCAGGAGTTTGAGACC TTTATAATCCCAGCACTTTGGGAGGCCAACGCGGGCGGATCACCTGAGGTCAGGAGTTTGAGACC A G ZNF146 Ensembl:ENSG00000167635 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs959970586 Functional Loss SNV dbSNP153 33..33 33 - - - 26363 RMVar_ID_26363 Human_SNP_ID_664702961 A-to-I Human chr19 + 36221053 36221053 36221053 TTTTGTATTTCTAGTAGAGACAGCGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACTT TTTTGTATTTCTAGTAGAGACAGCGTTTCACCGTGTTGGCCAGGCTGGTCTCGAACTCCTGACTT A G ZNF146 Ensembl:ENSG00000167635 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs989477378 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13439240,Human_RBP_ID_25406770 RMVar_hsa_circ_348160 26364 RMVar_ID_26364 Human_SNP_ID_664702963 A-to-I Human chr19 + 36221062 36221062 36221062 TCTAGTAGAGACAGCGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACTTCCTACTCGT TCTAGTAGAGACAGCGTTTCACCATGTTGGCCTGGCTGGTCTCGAACTCCTGACTTCCTACTCGT A T ZNF146 Ensembl:ENSG00000167635 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1182749925 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8484856,Human_RBP_ID_13439241,Human_RBP_ID_18729775 RMVar_hsa_circ_348160 26365 RMVar_ID_26365 Human_SNP_ID_664703878 A-to-I Human chr19 + 36223872 36223872 36223872 CGCTAATTTAAAAAAAAAAAAATTGTAGAGATAAGATCTCCCTGTGTTGCCCAGGCTGGTCTCAA CGCTAATTTAAAAAAAAAAAAATTGTAGAGATGAGATCTCCCTGTGTTGCCCAGGCTGGTCTCAA A G ZNF146 Ensembl:ENSG00000167635 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1161421571 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13439368 RMVar_hsa_circ_348160 26366 RMVar_ID_26366 Human_SNP_ID_664704752 A-to-I Human chr19 + 36227667 36227667 36227667 ATCTTGAACTCCTGGGCTCAAGTCATCCTCCCACCTCAGCCTCTTAAGTAGCTGAGACTACAGGC ATCTTGAACTCCTGGGCTCAAGTCATCCTCCCGCCTCAGCCTCTTAAGTAGCTGAGACTACAGGC A G ZNF146 Ensembl:ENSG00000167635 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1418877634 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_348160 26367 RMVar_ID_26367 Human_SNP_ID_664705842 A-to-I Human chr19 + 36232080 36232080 36232080 CAAAAACTAGCTGGGCGTGGTGATGCACACCTATCGTCCCAGCTACTCGGGAGGCTGAGGCAGGA CAAAAACTAGCTGGGCGTGGTGATGCACACCTGTCGTCCCAGCTACTCGGGAGGCTGAGGCAGGA A G ZNF146 Ensembl:ENSG00000167635 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1347923198 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25407082 26368 RMVar_ID_26368 Human_SNP_ID_664706040 A-to-I Human chr19 + 36232774 36232774 36232774 GGGATTATAGGAGCATGCCACCACATCCAGCTAATTTTTTGTATTTTTAGTAGAGACGAGGTTTC GGGATTATAGGAGCATGCCACCACATCCAGCTGATTTTTTGTATTTTTAGTAGAGACGAGGTTTC A G ZNF146 Ensembl:ENSG00000167635 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs535142929 Functional Loss SNV dbSNP153 33..33 33 - - - 26369 RMVar_ID_26369 Human_SNP_ID_664706168 A-to-I Human chr19 + 36233295 36233293 36233295 CAGCTACTTGGGAGGTTGAGGCTTCAAGAATCACTTGAAGCCAGGAGGCCGAGGTTGCAGTGAGT CAGCTACTTGGGAGGTTGAGGCTTCAAGAAT__CTTGAAGCCAGGAGGCCGAGGTTGCAGTGAGT TCA T ZNF146 Ensembl:ENSG00000167635 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1410544328 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_6748436,Human_RBP_ID_17568042 26370 RMVar_ID_26370 Human_SNP_ID_664726731 A-to-I Human chr19 - 36319873 36319873 36319873 CCCGGTAGGCAGAGCTTGCAGTGAGCCGAGATAGCGCCACTGCACTCCAGCCTGGGCGACAGAGG CCCGGTAGGCAGAGCTTGCAGTGAGCCGAGATTGCGCCACTGCACTCCAGCCTGGGCGACAGAGG T A LINC00665 Ensembl:ENSG00000232677 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs569602584 Functional Loss SNV dbSNP153 33..33 33 - - - 26371 RMVar_ID_26371 Human_SNP_ID_664726732 A-to-I Human chr19 - 36319873 36319873 36319873 CCCGGTAGGCAGAGCTTGCAGTGAGCCGAGATAGCGCCACTGCACTCCAGCCTGGGCGACAGAGG CCCGGTAGGCAGAGCTTGCAGTGAGCCGAGATCGCGCCACTGCACTCCAGCCTGGGCGACAGAGG T G LINC00665 Ensembl:ENSG00000232677 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs569602584 Functional Loss SNV dbSNP153 33..33 33 - - - 26372 RMVar_ID_26372 Human_SNP_ID_664726761 A-to-I Human chr19 - 36319958 36319958 36319958 AAAAATACAAAAAATTAGCTGGGCGTGGTGGCAGGCGCCTGTAGTCCCAGCTACTCGAGAGGCTG AAAAATACAAAAAATTAGCTGGGCGTGGTGGCGGGCGCCTGTAGTCCCAGCTACTCGAGAGGCTG T C LINC00665 Ensembl:ENSG00000232677 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs573320133 Functional Loss SNV dbSNP153 33..33 33 - - - 26373 RMVar_ID_26373 Human_SNP_ID_664726772 A-to-I Human chr19 - 36319986 36319986 36319986 GCCAACATGGTGAAACCCCCTCTCTACTAAAAATACAAAAAATTAGCTGGGCGTGGTGGCAGGCG GCCAACATGGTGAAACCCCCTCTCTACTAAAACTACAAAAAATTAGCTGGGCGTGGTGGCAGGCG T G LINC00665 Ensembl:ENSG00000232677 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1206007488 Functional Loss SNV dbSNP153 33..33 33 - - - 26374 RMVar_ID_26374 Human_SNP_ID_664726793 A-to-I Human chr19 - 36320088 36320088 36320088 AAGTGAAAAAGAGGCCAGCTGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGAAGGCTGAGGT AAGTGAAAAAGAGGCCAGCTGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGAAGGCTGAGGT T C LINC00665 Ensembl:ENSG00000232677 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1271061905 Functional Loss SNV dbSNP153 33..33 33 - - - 26375 RMVar_ID_26375 Human_SNP_ID_664726798 A-to-I Human chr19 - 36320098 36320098 36320098 CACTTTAGAAAAGTGAAAAAGAGGCCAGCTGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGA CACTTTAGAAAAGTGAAAAAGAGGCCAGCTGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGA T C LINC00665 Ensembl:ENSG00000232677 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs999922728 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20382230 26376 RMVar_ID_26376 Human_SNP_ID_664726908 A-to-I Human chr19 - 36320497 36320497 36320497 CCTTGGCCTCTCAAAGTGCTGGGATTACAGGCATGAGCCACCGCACCTGGCTGTTTTTTCATTTC CCTTGGCCTCTCAAAGTGCTGGGATTACAGGCCTGAGCCACCGCACCTGGCTGTTTTTTCATTTC T G LINC00665 Ensembl:ENSG00000232677 lincRNA intron GSE123020:GSM3490829,GSM3490830,GSM3490831 esophageal squamous carcinoma cells,EC109 cell line - 32596459 RNA-Seq:(High) rs551197025 Functional Loss SNV dbSNP153 33..33 33 - - - 26377 RMVar_ID_26377 Human_SNP_ID_664726944 A-to-I Human chr19 - 36320676 36320676 36320676 CCCTGCAAGAATCTGCCTCCCAGATTCACGCCATTTTCCCACCTCAGCCCCTGGAGTAGCTGGAA CCCTGCAAGAATCTGCCTCCCAGATTCACGCCGTTTTCCCACCTCAGCCCCTGGAGTAGCTGGAA T C LINC00665 Ensembl:ENSG00000232677 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1416801864 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5249032 Human_Splice_Rec_1998362,Human_Splice_Rec_1998372 26378 RMVar_ID_26378 Human_SNP_ID_664731375 A-to-I Human chr19 - 36338037 36338036 36338038 AGATCGTGCCACTGCACTCCAGCCTGGGTGACAGAGTGAGACCCTGTCTCAAAAAAAAAATTTGT AGATCGTGCCACTGCACTCCAGCCTGGGTGA__GAGTGAGACCCTGTCTCAAAAAAAAAATTTGT CTG C ZFP14 Ensembl:ENSG00000142065 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1478325465 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_194410,RMVar_hsa_circ_101147 26379 RMVar_ID_26379 Human_SNP_ID_664731398 A-to-I Human chr19 - 36338129 36338128 36338130 AAATTTAGCCAGGCATGGTGGCACACACCTGTAGTCCCAGGCTGAGGTGGGAGGATCACTTGAAC AAATTTAGCCAGGCATGGTGGCACACACCTG__GTCCCAGGCTGAGGTGGGAGGATCACTTGAAC CTA C ZFP14 Ensembl:ENSG00000142065 Protein coding 3'UTR GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1227840518 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_194410,RMVar_hsa_circ_101147 26380 RMVar_ID_26380 Human_SNP_ID_664731413 A-to-I Human chr19 - 36338203 36338203 36338203 GTGGATCACTTGAGGCCAGGAGTTTGAGACCAACCTGGTTAACATGGTGAAACCCTGTCTGTACT GTGGATCACTTGAGGCCAGGAGTTTGAGACCAGCCTGGTTAACATGGTGAAACCCTGTCTGTACT T C ZFP14 Ensembl:ENSG00000142065 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1245170774 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_194410,RMVar_hsa_circ_101147 26381 RMVar_ID_26381 Human_SNP_ID_664757911 A-to-I Human chr19 - 36445657 36445657 36445657 ATGCCACTACGCCTGGAAAATTTTGTATTTTTAGTAGAGACGGCATTTTTCCATGTTGGTCAGGC ATGCCACTACGCCTGGAAAATTTTGTATTTTTGGTAGAGACGGCATTTTTCCATGTTGGTCAGGC T C ZNF566 Ensembl:ENSG00000186017 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs191807139 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13440709 RMVar_hsa_circ_194413 26382 RMVar_ID_26382 Human_SNP_ID_664758086 A-to-I Human chr19 - 36446393 36446393 36446393 GTGGCATGTGCCTGTAGTCCCAGCTGCTCGGAAGGCTGAGGCAGGAGAATCGCTTGAACCCGGGA GTGGCATGTGCCTGTAGTCCCAGCTGCTCGGAGGGCTGAGGCAGGAGAATCGCTTGAACCCGGGA T C ZNF566 Ensembl:ENSG00000186017 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs937984224 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_194413 26383 RMVar_ID_26383 Human_SNP_ID_664758102 A-to-I Human chr19 - 36446471 36446471 36446471 GAGGCCAAGGCAGGGGGCAGCCTGGCCAATATAGTGAAACCCCATCTCTACTAAAAATACAAAAA GAGGCCAAGGCAGGGGGCAGCCTGGCCAATATGGTGAAACCCCATCTCTACTAAAAATACAAAAA T C ZNF566 Ensembl:ENSG00000186017 Protein coding intron GSE47997;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 K562 cells&HepG2 cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 23474544,29129909,31158229 RNA-Seq:(High) rs914248711 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25407637 RMVar_hsa_circ_194413 26384 RMVar_ID_26384 Human_SNP_ID_664758110 A-to-I Human chr19 - 36446518 36446518 36446518 AAAGGGGCTGGGCACAGTGGCTTACGCCTGTAATCCCAGTGCTTTGGGAGGCCAAGGCAGGGGGC AAAGGGGCTGGGCACAGTGGCTTACGCCTGTAGTCCCAGTGCTTTGGGAGGCCAAGGCAGGGGGC T C ZNF566 Ensembl:ENSG00000186017 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1253869833 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_194413 26385 RMVar_ID_26385 Human_SNP_ID_664762014 A-to-I Human chr19 - 36462835 36462835 36462835 CTCCTACCTCAGCCTCTCGAGTAGCTTGGATTACAGGCACCCCCCACCACGCCTGGCTAATTTTT CTCCTACCTCAGCCTCTCGAGTAGCTTGGATTGCAGGCACCCCCCACCACGCCTGGCTAATTTTT T C ZNF566 Ensembl:ENSG00000186017 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs901820894 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8485177 26386 RMVar_ID_26386 Human_SNP_ID_664762515 A-to-I Human chr19 - 36464692 36464692 36464692 ACGGCTCACTGCAGCTTCTACCTCCTAGGCTCAGGTGATCCTCCCACCTCAGCCTCCCAGGACTG ACGGCTCACTGCAGCTTCTACCTCCTAGGCTCCGGTGATCCTCCCACCTCAGCCTCCCAGGACTG T G ZNF566 Ensembl:ENSG00000186017 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170894127 Functional Loss SNV dbSNP153 33..33 33 - - - 26387 RMVar_ID_26387 Human_SNP_ID_664762516 A-to-I Human chr19 - 36464698 36464698 36464698 ACAATCACGGCTCACTGCAGCTTCTACCTCCTAGGCTCAGGTGATCCTCCCACCTCAGCCTCCCA ACAATCACGGCTCACTGCAGCTTCTACCTCCTTGGCTCAGGTGATCCTCCCACCTCAGCCTCCCA T A ZNF566 Ensembl:ENSG00000186017 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs541905807 Functional Loss SNV dbSNP153 33..33 33 - - - 26388 RMVar_ID_26388 Human_SNP_ID_664775975 A-to-I Human chr19 - 36516489 36516489 36516489 AAATCCTGGGCCTAAGCAATCTGCCCACCTCAATCTCCTCAGTAGCTAGGACTACAGGCACCATG AAATCCTGGGCCTAAGCAATCTGCCCACCTCAGTCTCCTCAGTAGCTAGGACTACAGGCACCATG T C ZNF260 Ensembl:ENSG00000254004 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1043784021 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_194417,RMVar_hsa_circ_121682 26389 RMVar_ID_26389 Human_SNP_ID_664775976 A-to-I Human chr19 - 36516489 36516489 36516489 AAATCCTGGGCCTAAGCAATCTGCCCACCTCAATCTCCTCAGTAGCTAGGACTACAGGCACCATG AAATCCTGGGCCTAAGCAATCTGCCCACCTCACTCTCCTCAGTAGCTAGGACTACAGGCACCATG T G ZNF260 Ensembl:ENSG00000254004 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1043784021 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_194417,RMVar_hsa_circ_121682 26390 RMVar_ID_26390 Human_SNP_ID_664775979 A-to-I Human chr19 - 36516495 36516495 36516495 GCCCTGAAATCCTGGGCCTAAGCAATCTGCCCACCTCAATCTCCTCAGTAGCTAGGACTACAGGC GCCCTGAAATCCTGGGCCTAAGCAATCTGCCCGCCTCAATCTCCTCAGTAGCTAGGACTACAGGC T C ZNF260 Ensembl:ENSG00000254004 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs912898149 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_194417,RMVar_hsa_circ_121682 26391 RMVar_ID_26391 Human_SNP_ID_664776191 A-to-I Human chr19 - 36517300 36517300 36517300 GCCTCGAACTCCTGGGCTCAAGCGATCCTCCTACTTCAACCTCCCAAGTAACTAAGACTACAGGT GCCTCGAACTCCTGGGCTCAAGCGATCCTCCTGCTTCAACCTCCCAAGTAACTAAGACTACAGGT T C ZNF260 Ensembl:ENSG00000254004 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1274097756 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1998520,Human_Splice_Rec_1998521 RMVar_hsa_circ_194417,RMVar_hsa_circ_121682 26392 RMVar_ID_26392 Human_SNP_ID_664776192 A-to-I Human chr19 - 36517300 36517300 36517300 GCCTCGAACTCCTGGGCTCAAGCGATCCTCCTACTTCAACCTCCCAAGTAACTAAGACTACAGGT GCCTCGAACTCCTGGGCTCAAGCGATCCTCCTCCTTCAACCTCCCAAGTAACTAAGACTACAGGT T G ZNF260 Ensembl:ENSG00000254004 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1274097756 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1998520,Human_Splice_Rec_1998521 RMVar_hsa_circ_194417,RMVar_hsa_circ_121682 26393 RMVar_ID_26393 Human_SNP_ID_664777851 A-to-I Human chr19 - 36524314 36524314 36524314 AAAATTAGCCAGGTGTGGTGGCGGGCGCCTGTAGTTCCAGCTACTCAGGAGGCTGAGGTGGGAGA AAAATTAGCCAGGTGTGGTGGCGGGCGCCTGTGGTTCCAGCTACTCAGGAGGCTGAGGTGGGAGA T C ZNF260 Ensembl:ENSG00000254004 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs918696309 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_194417,RMVar_hsa_circ_121682 26394 RMVar_ID_26394 Human_SNP_ID_664783207 A-to-I Human chr19 - 36546087 36546081 36546087 TATACTATATATGCCCACACATGCACTACATAACACACTATATATATATATATATATACACACAC TATACTATATATGCCCACACATGCACTACATA______TATATATATATATATATATACACACAC AGTGTGT A ZNF529 Ensembl:ENSG00000186020 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1262588784 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_6750254,Human_RBP_ID_8256017,Human_RBP_ID_17383447,Human_RBP_ID_17499365,Human_RBP_ID_18304108,Human_RBP_ID_27678123 26395 RMVar_ID_26395 Human_SNP_ID_664783226 A-to-I Human chr19 - 36546133 36546133 36546133 TATACTATATGTGTGTATATAGTGTGTGATGTATATGTGTGTGATGTATACTATATATGCCCACA TATACTATATGTGTGTATATAGTGTGTGATGTGTATGTGTGTGATGTATACTATATATGCCCACA T C ZNF529 Ensembl:ENSG00000186020 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs995940847 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3569525,Human_RBP_ID_6750255,Human_RBP_ID_8485279,Human_RBP_ID_18304109,Human_RBP_ID_22502550,Human_RBP_ID_27678123 26396 RMVar_ID_26396 Human_SNP_ID_664783283 A-to-I Human chr19 - 36546272 36546272 36546272 CCCCCAAAAAAACACATACATAGGAACTGGTTATATTCCACCATAACACACACACACACACACAC CCCCCAAAAAAACACATACATAGGAACTGGTTGTATTCCACCATAACACACACACACACACACAC T C ZNF529 Ensembl:ENSG00000186020 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs938249771 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6750258 Human_miRNA_ID_152011,Human_miRNA_ID_1211981 26397 RMVar_ID_26397 Human_SNP_ID_664790482 A-to-I Human chr19 + 36577162 36577161 36577163 TTGTATTTTAGGTGGAGACAAGGTTTCGCCACATTGACTGGGCTGGTCTGGAACTCCTGAGCTCA TTGTATTTTAGGTGGAGACAAGGTTTCGCCAC__TGACTGGGCTGGTCTGGAACTCCTGAGCTCA CAT C ZNF529-AS1 Ensembl:ENSG00000233527 lincRNA intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs754881794 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_4523512 Human_Splice_Rec_1998598,Human_Splice_Rec_1998604 26398 RMVar_ID_26398 Human_SNP_ID_664790483 A-to-I Human chr19 + 36577162 36577162 36577162 TTGTATTTTAGGTGGAGACAAGGTTTCGCCACATTGACTGGGCTGGTCTGGAACTCCTGAGCTCA TTGTATTTTAGGTGGAGACAAGGTTTCGCCACGTTGACTGGGCTGGTCTGGAACTCCTGAGCTCA A G ZNF529-AS1 Ensembl:ENSG00000233527 lincRNA intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1046168798 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4523512 Human_Splice_Rec_1998598,Human_Splice_Rec_1998604 26399 RMVar_ID_26399 Human_SNP_ID_664790510 A-to-I Human chr19 + 36577228 36577228 36577228 GCAACCGGCCCTCCTTGACCTCCCAAAGTGCTAGGATTACAGGTGTGAACCACCGTGCCCGGCCC GCAACCGGCCCTCCTTGACCTCCCAAAGTGCTGGGATTACAGGTGTGAACCACCGTGCCCGGCCC A G ZNF529-AS1 Ensembl:ENSG00000233527 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1221051480 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1998598,Human_Splice_Rec_1998599,Human_Splice_Rec_1998604,Human_Splice_Rec_1998619 26400 RMVar_ID_26400 Human_SNP_ID_664791436 A-to-I Human chr19 + 36581000 36581000 36581000 AAACTTGGGCATCTGTAGGTTTTGGTATCCACAAGGTGTCCTGGAACCAGTCCCCTGTGGATAGC AAACTTGGGCATCTGTAGGTTTTGGTATCCACCAGGTGTCCTGGAACCAGTCCCCTGTGGATAGC A C ZNF529-AS1 Ensembl:ENSG00000233527 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1057329921 Functional Loss SNV dbSNP153 33..33 33 - - - 26401 RMVar_ID_26401 Human_SNP_ID_664791437 A-to-I Human chr19 + 36581000 36581000 36581000 AAACTTGGGCATCTGTAGGTTTTGGTATCCACAAGGTGTCCTGGAACCAGTCCCCTGTGGATAGC AAACTTGGGCATCTGTAGGTTTTGGTATCCACGAGGTGTCCTGGAACCAGTCCCCTGTGGATAGC A G ZNF529-AS1 Ensembl:ENSG00000233527 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1057329921 Functional Loss SNV dbSNP153 33..33 33 - - - 26402 RMVar_ID_26402 Human_SNP_ID_664804710 A-to-I Human chr19 - 36639435 36639435 36639435 GAATTCACACTGGTGAGAAACCTTATGAATGTAAAGAATGTGGGAAGGCCTTTAGACAGCGATCA GAATTCACACTGGTGAGAAACCTTATGAATGTGAAGAATGTGGGAAGGCCTTTAGACAGCGATCA T C ZNF461 Ensembl:ENSG00000197808 Protein coding CDS GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs376344953 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1885559 Human_miRNA_ID_109635,Human_miRNA_ID_837158 26403 RMVar_ID_26403 Human_SNP_ID_664804713 A-to-I Human chr19 - 36639443 36639443 36639443 ACATCAAAGAATTCACACTGGTGAGAAACCTTATGAATGTAAAGAATGTGGGAAGGCCTTTAGAC ACATCAAAGAATTCACACTGGTGAGAAACCTTGTGAATGTAAAGAATGTGGGAAGGCCTTTAGAC T C ZNF461 Ensembl:ENSG00000197808 Protein coding CDS GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1295837634 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_109635,Human_miRNA_ID_837158 26404 RMVar_ID_26404 Human_SNP_ID_664828971 A-to-I Human chr19 - 36745511 36745511 36745511 ACCATGCCCGACTAATTTTTGTATTATTTAGTAGAGACGGGGTTTCTCCATGTTGGTCAGGCTGG ACCATGCCCGACTAATTTTTGTATTATTTAGTGGAGACGGGGTTTCTCCATGTTGGTCAGGCTGG T C ZNF850 Ensembl:ENSG00000267041 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1226609671 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267417 26405 RMVar_ID_26405 Human_SNP_ID_664828981 A-to-I Human chr19 - 36745556 36745556 36745556 CTCTTGACTCAGCCTCCTGAGTAACTGGGATTACAGGCATGCTCCACCATGCCCGACTAATTTTT CTCTTGACTCAGCCTCCTGAGTAACTGGGATTGCAGGCATGCTCCACCATGCCCGACTAATTTTT T C ZNF850 Ensembl:ENSG00000267041 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1259301122 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267417 26406 RMVar_ID_26406 Human_SNP_ID_664828995 A-to-I Human chr19 - 36745615 36745615 36745615 GGAGTGCAATGGCACGATCTTGGCTCACTGCAACCTCCGCCTCCCAGGTTCAAGCGATTCTCTTG GGAGTGCAATGGCACGATCTTGGCTCACTGCAGCCTCCGCCTCCCAGGTTCAAGCGATTCTCTTG T C ZNF850 Ensembl:ENSG00000267041 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1408687998 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267417 26407 RMVar_ID_26407 Human_SNP_ID_664828996 A-to-I Human chr19 - 36745616 36745616 36745616 TGGAGTGCAATGGCACGATCTTGGCTCACTGCAACCTCCGCCTCCCAGGTTCAAGCGATTCTCTT TGGAGTGCAATGGCACGATCTTGGCTCACTGCGACCTCCGCCTCCCAGGTTCAAGCGATTCTCTT T C ZNF850 Ensembl:ENSG00000267041 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1418396827 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267417 26408 RMVar_ID_26408 Human_SNP_ID_664829176 A-to-I Human chr19 - 36746515 36746515 36746515 TGAAACCCCATCTCTACTAAAAATACAAAATCAGCCAGACATGGTGGCATATGCCTGTAATCCCA TGAAACCCCATCTCTACTAAAAATACAAAATCCGCCAGACATGGTGGCATATGCCTGTAATCCCA T G ZNF850 Ensembl:ENSG00000267041 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1448527715 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267417 26409 RMVar_ID_26409 Human_SNP_ID_664829180 A-to-I Human chr19 - 36746528 36746528 36746528 CTGGCCAACATGTTGAAACCCCATCTCTACTAAAAATACAAAATCAGCCAGACATGGTGGCATAT CTGGCCAACATGTTGAAACCCCATCTCTACTAGAAATACAAAATCAGCCAGACATGGTGGCATAT T C ZNF850 Ensembl:ENSG00000267041 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1242974608 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267417 26410 RMVar_ID_26410 Human_SNP_ID_664829186 A-to-I Human chr19 - 36746553 36746553 36746553 CTGAGGTTAAGAGTTCAAGACCAGCCTGGCCAACATGTTGAAACCCCATCTCTACTAAAAATACA CTGAGGTTAAGAGTTCAAGACCAGCCTGGCCAGCATGTTGAAACCCCATCTCTACTAAAAATACA T C ZNF850 Ensembl:ENSG00000267041 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1420139630 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267417 26411 RMVar_ID_26411 Human_SNP_ID_664829187 A-to-I Human chr19 - 36746554 36746554 36746554 CCTGAGGTTAAGAGTTCAAGACCAGCCTGGCCAACATGTTGAAACCCCATCTCTACTAAAAATAC CCTGAGGTTAAGAGTTCAAGACCAGCCTGGCCGACATGTTGAAACCCCATCTCTACTAAAAATAC T C ZNF850 Ensembl:ENSG00000267041 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs943381908 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267417 26412 RMVar_ID_26412 Human_SNP_ID_664842723 A-to-I Human chr19 + 36802501 36802501 36802501 CTCTGTTGCCCAGGCTGGTGTGTAGTGATCTCAGCTCACTGCAAGCTCCACCTTCCGGGTTCACA CTCTGTTGCCCAGGCTGGTGTGTAGTGATCTCTGCTCACTGCAAGCTCCACCTTCCGGGTTCACA A T ZNF790-AS1 Ensembl:ENSG00000267254 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1396748662 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6752270 Human_Splice_Rec_1998854,Human_Splice_Rec_1998860 26413 RMVar_ID_26413 Human_SNP_ID_664843805 A-to-I Human chr19 + 36806848 36806848 36806848 CATCCTGGCTAACACGGTGAAACCTCGTCTCTACTAAAAAAAATACAAAAAATTAGCCGGGCATG CATCCTGGCTAACACGGTGAAACCTCGTCTCTGCTAAAAAAAATACAAAAAATTAGCCGGGCATG A G ZNF790-AS1 Ensembl:ENSG00000267254 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1263816928 Functional Loss SNV dbSNP153 33..33 33 - - - 26414 RMVar_ID_26414 Human_SNP_ID_664843818 A-to-I Human chr19 + 36806894 36806894 36806894 AAAAAATTAGCCGGGCATGGTGGCAGGTGCCTATAGTCCCAGCTACTCGGAGGCTGAGGCAGGAG AAAAAATTAGCCGGGCATGGTGGCAGGTGCCTGTAGTCCCAGCTACTCGGAGGCTGAGGCAGGAG A G ZNF790-AS1 Ensembl:ENSG00000267254 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs78193269 Functional Loss SNV dbSNP153 33..33 33 - - - 26415 RMVar_ID_26415 Human_SNP_ID_664843822 A-to-I Human chr19 + 36806906 36806906 36806906 GGGCATGGTGGCAGGTGCCTATAGTCCCAGCTACTCGGAGGCTGAGGCAGGAGAATGGCGTGAAC GGGCATGGTGGCAGGTGCCTATAGTCCCAGCTCCTCGGAGGCTGAGGCAGGAGAATGGCGTGAAC A C ZNF790-AS1 Ensembl:ENSG00000267254 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs886860045 Functional Loss SNV dbSNP153 33..33 33 - - - 26416 RMVar_ID_26416 Human_SNP_ID_664845810 A-to-I Human chr19 - 36816412 36816412 36816412 GTGGTGGCACATGCCTCTGGTCCCAGCTACTCAGGAGGCTGAGGTGAGAGGACTGCTTGGGCCCA GTGGTGGCACATGCCTCTGGTCCCAGCTACTCCGGAGGCTGAGGTGAGAGGACTGCTTGGGCCCA T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1009180366 Functional Loss SNV dbSNP153 33..33 33 - - - 26417 RMVar_ID_26417 Human_SNP_ID_664863342 A-to-I Human chr19 - 36888901 36888901 36888901 TGGGCATGGTGGCAGGCACTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATTACTTGAA TGGGCATGGTGGCAGGCACTGTAGTCCCAGCTCCTTGGGAGGCTGAGGCAGGAGAATTACTTGAA T G ZNF829 Ensembl:ENSG00000185869 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1215302018 Functional Loss SNV dbSNP153 33..33 33 - - - 26418 RMVar_ID_26418 Human_SNP_ID_664934249 A-to-I Human chr19 - 37190319 37190319 37190319 ATCACTTGAACCCGGGAGGTGGAGGTTGCAGTAAGCCAAGATCGCGCCACTGCACTCCAGCCTGG ATCACTTGAACCCGGGAGGTGGAGGTTGCAGTGAGCCAAGATCGCGCCACTGCACTCCAGCCTGG T C ZNF585B,AC012309.1 Ensembl:ENSG00000245680,Ensembl:ENSG00000267360 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs556742348 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_138925 RMVar_hsa_circ_8577,RMVar_hsa_circ_109459,RMVar_hsa_circ_194461,RMVar_hsa_circ_313615,RMVar_hsa_circ_194464,RMVar_hsa_circ_76346,RMVar_hsa_circ_194465,RMVar_hsa_circ_336922,RMVar_hsa_circ_277750,RMVar_hsa_circ_194467,RMVar_hsa_circ_194466,RMVar_hsa_circ_371501 26419 RMVar_ID_26419 Human_SNP_ID_664934264 A-to-I Human chr19 - 37190370 37190370 37190370 GTGGTGGCACGTGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCCG GTGGTGGCACGTGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCCG T C ZNF585B,AC012309.1 Ensembl:ENSG00000245680,Ensembl:ENSG00000267360 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs910550154 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_138925 RMVar_hsa_circ_8577,RMVar_hsa_circ_109459,RMVar_hsa_circ_194461,RMVar_hsa_circ_313615,RMVar_hsa_circ_194464,RMVar_hsa_circ_76346,RMVar_hsa_circ_194465,RMVar_hsa_circ_336922,RMVar_hsa_circ_277750,RMVar_hsa_circ_194467,RMVar_hsa_circ_194466,RMVar_hsa_circ_371501 26420 RMVar_ID_26420 Human_SNP_ID_664934265 A-to-I Human chr19 - 37190370 37190370 37190370 GTGGTGGCACGTGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCCG GTGGTGGCACGTGCCTGTAATCCCAGCTACTCCGGAGGCTGAGGCAGGAGAATCACTTGAACCCG T G ZNF585B,AC012309.1 Ensembl:ENSG00000245680,Ensembl:ENSG00000267360 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs910550154 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_138925 RMVar_hsa_circ_8577,RMVar_hsa_circ_109459,RMVar_hsa_circ_194461,RMVar_hsa_circ_313615,RMVar_hsa_circ_194464,RMVar_hsa_circ_76346,RMVar_hsa_circ_194465,RMVar_hsa_circ_336922,RMVar_hsa_circ_277750,RMVar_hsa_circ_194467,RMVar_hsa_circ_194466,RMVar_hsa_circ_371501 26421 RMVar_ID_26421 Human_SNP_ID_664948107 A-to-I Human chr19 + 37245104 37245104 37245104 CACAAGGTCTGAAGATTAAGGCCATCCTGGCTAACAGTGAAACCCCGTCTCTACTTAGCTGGGCG CACAAGGTCTGAAGATTAAGGCCATCCTGGCTCACAGTGAAACCCCGTCTCTACTTAGCTGGGCG A C ZNF383 Ensembl:ENSG00000188283 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs972561812 Functional Loss SNV dbSNP153 33..33 33 - - - 26422 RMVar_ID_26422 Human_SNP_ID_664948314 A-to-I Human chr19 + 37245716 37245716 37245716 AGGCTGGTCTTGAACTCTTGACCTTGTGATCCACCCACCTCGGCCTCCCAAAGTTCGGGGATTAC AGGCTGGTCTTGAACTCTTGACCTTGTGATCCTCCCACCTCGGCCTCCCAAAGTTCGGGGATTAC A T ZNF383 Ensembl:ENSG00000188283 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1451215544 Functional Loss SNV dbSNP153 33..33 33 - - - 26423 RMVar_ID_26423 Human_SNP_ID_664968757 A-to-I Human chr19 + 37324876 37324876 37324876 TGCTCACTGCAAGCTCTGCCTTCCGGGTTCACACCATTCTCCCACCTCAGCCCCTGGAGTAGTTG TGCTCACTGCAAGCTCTGCCTTCCGGGTTCACGCCATTCTCCCACCTCAGCCCCTGGAGTAGTTG A G ZNF875 Ensembl:ENSG00000181666 Protein coding 5'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973741572 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17923264,Human_RBP_ID_18730922,Human_RBP_ID_25410843 Human_Splice_Rec_1999578,Human_Splice_Rec_1999579,Human_Splice_Rec_1999598,Human_Splice_Rec_1999599,Human_Splice_Rec_1999626,Human_Splice_Rec_1999627,Human_Splice_Rec_1999664 RMVar_hsa_circ_21292,RMVar_hsa_circ_39455 26424 RMVar_ID_26424 Human_SNP_ID_664968758 A-to-I Human chr19 + 37324876 37324876 37324876 TGCTCACTGCAAGCTCTGCCTTCCGGGTTCACACCATTCTCCCACCTCAGCCCCTGGAGTAGTTG TGCTCACTGCAAGCTCTGCCTTCCGGGTTCACTCCATTCTCCCACCTCAGCCCCTGGAGTAGTTG A T ZNF875 Ensembl:ENSG00000181666 Protein coding 5'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973741572 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17923264,Human_RBP_ID_18730922,Human_RBP_ID_25410843 Human_Splice_Rec_1999578,Human_Splice_Rec_1999579,Human_Splice_Rec_1999598,Human_Splice_Rec_1999599,Human_Splice_Rec_1999626,Human_Splice_Rec_1999627,Human_Splice_Rec_1999664 RMVar_hsa_circ_21292,RMVar_hsa_circ_39455 26425 RMVar_ID_26425 Human_SNP_ID_664968760 A-to-I Human chr19 + 37324887 37324887 37324887 AGCTCTGCCTTCCGGGTTCACACCATTCTCCCACCTCAGCCCCTGGAGTAGTTGGGACTACAGGC AGCTCTGCCTTCCGGGTTCACACCATTCTCCCCCCTCAGCCCCTGGAGTAGTTGGGACTACAGGC A C ZNF875 Ensembl:ENSG00000181666 Protein coding 5'UTR GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank;Bronchiolar epithelium,BEP2D cell line - 29129909,30559470,31158229 RNA-Seq:(High) rs1268907232 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13444873,Human_RBP_ID_17923264,Human_RBP_ID_18730922,Human_RBP_ID_25410845 Human_Splice_Rec_1999578,Human_Splice_Rec_1999579,Human_Splice_Rec_1999598,Human_Splice_Rec_1999599,Human_Splice_Rec_1999626,Human_Splice_Rec_1999627,Human_Splice_Rec_1999664 RMVar_hsa_circ_21292,RMVar_hsa_circ_39455 26426 RMVar_ID_26426 Human_SNP_ID_664968763 A-to-I Human chr19 + 37324914 37324914 37324914 CTCCCACCTCAGCCCCTGGAGTAGTTGGGACTACAGGCTCATGCTACCACACCTGGTTAATTTTG CTCCCACCTCAGCCCCTGGAGTAGTTGGGACTGCAGGCTCATGCTACCACACCTGGTTAATTTTG A G ZNF875 Ensembl:ENSG00000181666 Protein coding 5'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs926833932 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6755204,Human_RBP_ID_13444873 Human_Splice_Rec_1999579,Human_Splice_Rec_1999599,Human_Splice_Rec_1999627 RMVar_hsa_circ_21292,RMVar_hsa_circ_39455 26427 RMVar_ID_26427 Human_SNP_ID_664968780 A-to-I Human chr19 + 37324963 37324963 37324963 CACCTGGTTAATTTTGTTTTTGTGTTTTTAGTAGAAACGGGGTTTCACCGTGTTGGCCAGGATGG CACCTGGTTAATTTTGTTTTTGTGTTTTTAGTGGAAACGGGGTTTCACCGTGTTGGCCAGGATGG A G ZNF875 Ensembl:ENSG00000181666 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs918064673 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21292 26428 RMVar_ID_26428 Human_SNP_ID_664968781 A-to-I Human chr19 + 37324963 37324963 37324963 CACCTGGTTAATTTTGTTTTTGTGTTTTTAGTAGAAACGGGGTTTCACCGTGTTGGCCAGGATGG CACCTGGTTAATTTTGTTTTTGTGTTTTTAGTTGAAACGGGGTTTCACCGTGTTGGCCAGGATGG A T ZNF875 Ensembl:ENSG00000181666 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs918064673 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21292 26429 RMVar_ID_26429 Human_SNP_ID_664968802 A-to-I Human chr19 + 37325030 37325030 37325030 TGGATCTCCTGACCTCGTGATCTGCCCACCTCAGCCTCTCAAAGTGCTGGGATTACAGGCCTGAG TGGATCTCCTGACCTCGTGATCTGCCCACCTCCGCCTCTCAAAGTGCTGGGATTACAGGCCTGAG A C ZNF875 Ensembl:ENSG00000181666 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1429563790 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21292 26430 RMVar_ID_26430 Human_SNP_ID_664968806 A-to-I Human chr19 + 37325039 37325039 37325039 TGACCTCGTGATCTGCCCACCTCAGCCTCTCAAAGTGCTGGGATTACAGGCCTGAGCCACTGTGC TGACCTCGTGATCTGCCCACCTCAGCCTCTCAGAGTGCTGGGATTACAGGCCTGAGCCACTGTGC A G ZNF875 Ensembl:ENSG00000181666 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs1029615660 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21292 26431 RMVar_ID_26431 Human_SNP_ID_664969264 A-to-I Human chr19 + 37326902 37326902 37326902 TTTGGCTAGCCTGGTCTTGAACTCTTGACCTCAAGTGATCTGCCCGCCTCAGCCTCCCAAAGTGC TTTGGCTAGCCTGGTCTTGAACTCTTGACCTCGAGTGATCTGCCCGCCTCAGCCTCCCAAAGTGC A G ZNF875 Ensembl:ENSG00000181666 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs768138739 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21292 26432 RMVar_ID_26432 Human_SNP_ID_664969594 A-to-I Human chr19 + 37328080 37328080 37328080 CCTGACCAACACGGAGAAACCCCATCTTTACTAAAAATACAAATTAGCTGGGTGTGGTGGTGCAT CCTGACCAACACGGAGAAACCCCATCTTTACTGAAAATACAAATTAGCTGGGTGTGGTGGTGCAT A G ZNF875 Ensembl:ENSG00000181666 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348970272 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26467759 RMVar_hsa_circ_21292 26433 RMVar_ID_26433 Human_SNP_ID_664969618 A-to-I Human chr19 + 37328188 37328188 37328188 CTTGAACTGGGAGGTGGAGCCTGCAGTAAGCCAAGATCGCACCATTGCACTCCAGCCTGGTTAAC CTTGAACTGGGAGGTGGAGCCTGCAGTAAGCCCAGATCGCACCATTGCACTCCAGCCTGGTTAAC A C ZNF875 Ensembl:ENSG00000181666 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs942713322 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17568045,Human_RBP_ID_26467761 RMVar_hsa_circ_21292 26434 RMVar_ID_26434 Human_SNP_ID_664972211 A-to-I Human chr19 + 37337474 37337474 37337474 GGACTTAAGGGGAAGCGTTCTTCTTTTTTTTGAAACGGATTCTCGGTCTGTCTTCCGGGCTGGTG GGACTTAAGGGGAAGCGTTCTTCTTTTTTTTGGAACGGATTCTCGGTCTGTCTTCCGGGCTGGTG A G ZNF875,AC016590.2 Ensembl:ENSG00000181666,Ensembl:ENSG00000267682 Protein coding,lincRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1182612995 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5248858,Human_RBP_ID_13445176,Human_RBP_ID_20385818,Human_RBP_ID_23177169 Human_miRNA_ID_3212581 RMVar_hsa_circ_21292,RMVar_hsa_circ_304734 26435 RMVar_ID_26435 Human_SNP_ID_664972230 A-to-I Human chr19 + 37337514 37337514 37337514 TCTCGGTCTGTCTTCCGGGCTGGTGCGATCTCAGCTCACTGCACCCTCTGCCTCCCAGGTTCAAA TCTCGGTCTGTCTTCCGGGCTGGTGCGATCTCGGCTCACTGCACCCTCTGCCTCCCAGGTTCAAA A G ZNF875,AC016590.2 Ensembl:ENSG00000181666,Ensembl:ENSG00000267682 Protein coding,lincRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1203415799 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5193126,Human_RBP_ID_5248858,Human_RBP_ID_8200092,Human_RBP_ID_13445179 Human_Splice_Rec_1999791 Human_miRNA_ID_3165796 RMVar_hsa_circ_21292,RMVar_hsa_circ_304734 26436 RMVar_ID_26436 Human_SNP_ID_664972239 A-to-I Human chr19 + 37337544 37337544 37337544 TCAGCTCACTGCACCCTCTGCCTCCCAGGTTCAAACGATTCTCCTGTCCCAGCCTCCCGAGTAGC TCAGCTCACTGCACCCTCTGCCTCCCAGGTTCGAACGATTCTCCTGTCCCAGCCTCCCGAGTAGC A G ZNF875,AC016590.2 Ensembl:ENSG00000181666,Ensembl:ENSG00000267682 Protein coding,lincRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355432970 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5248858 Human_Splice_Rec_1999791 RMVar_hsa_circ_21292,RMVar_hsa_circ_304734 26437 RMVar_ID_26437 Human_SNP_ID_664973655 A-to-I Human chr19 + 37343056 37343056 37343056 CCAACTTAGTGGCCTAAAGAACATAGCGGCTTAGGCCTGGTACAGTGGCTCTCACCTGTAATCCC CCAACTTAGTGGCCTAAAGAACATAGCGGCTTCGGCCTGGTACAGTGGCTCTCACCTGTAATCCC A C ZNF875 Ensembl:ENSG00000181666 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs113686052 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13445425 RMVar_hsa_circ_21292,RMVar_hsa_circ_304734 26438 RMVar_ID_26438 Human_SNP_ID_664973656 A-to-I Human chr19 + 37343056 37343056 37343056 CCAACTTAGTGGCCTAAAGAACATAGCGGCTTAGGCCTGGTACAGTGGCTCTCACCTGTAATCCC CCAACTTAGTGGCCTAAAGAACATAGCGGCTTTGGCCTGGTACAGTGGCTCTCACCTGTAATCCC A T ZNF875 Ensembl:ENSG00000181666 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs113686052 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13445425 RMVar_hsa_circ_21292,RMVar_hsa_circ_304734 26439 RMVar_ID_26439 Human_SNP_ID_664978334 A-to-I Human chr19 + 37361715 37361715 37361715 GGAGGCTTAGGCTGACCTGAGGTCAGGAGTTCAAGACCAGCCTGGCAAACACGGTAAAACTCTGT GGAGGCTTAGGCTGACCTGAGGTCAGGAGTTCGAGACCAGCCTGGCAAACACGGTAAAACTCTGT A G ZNF875 Ensembl:ENSG00000181666 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1250892987 Functional Loss SNV dbSNP153 33..33 33 - - - 26440 RMVar_ID_26440 Human_SNP_ID_664978342 A-to-I Human chr19 + 37361755 37361755 37361755 CCTGGCAAACACGGTAAAACTCTGTCTCTACTAAAAATACAAAAATTAGCTGGGCGTAGTCTTGG CCTGGCAAACACGGTAAAACTCTGTCTCTACTGAAAATACAAAAATTAGCTGGGCGTAGTCTTGG A G ZNF875 Ensembl:ENSG00000181666 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs776935010 Functional Loss SNV dbSNP153 33..33 33 - - - 26441 RMVar_ID_26441 Human_SNP_ID_664985779 A-to-I Human chr19 + 37390231 37390231 37390231 TTGTATTTTTAGTAGAGACGGGGTTTCACCACATTGGTCAGGCTGATCTCGAACTCCTGACTTTA TTGTATTTTTAGTAGAGACGGGGTTTCACCACGTTGGTCAGGCTGATCTCGAACTCCTGACTTTA A G ZNF527 Ensembl:ENSG00000189164 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1401191626 Functional Loss SNV dbSNP153 33..33 33 - - - 26442 RMVar_ID_26442 Human_SNP_ID_664985794 A-to-I Human chr19 + 37390290 37390290 37390290 ACTTTAGGTGATCCACACGCCTCAGACTCCCAAAGTGCTGGGATTATGGGCGTGAGCCACCGCGC ACTTTAGGTGATCCACACGCCTCAGACTCCCAGAGTGCTGGGATTATGGGCGTGAGCCACCGCGC A G ZNF527 Ensembl:ENSG00000189164 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1016449540 Functional Loss SNV dbSNP153 33..33 33 - - - 26443 RMVar_ID_26443 Human_SNP_ID_664985797 A-to-I Human chr19 + 37390303 37390303 37390303 CACACGCCTCAGACTCCCAAAGTGCTGGGATTATGGGCGTGAGCCACCGCGCCTGGCCACATCTG CACACGCCTCAGACTCCCAAAGTGCTGGGATTGTGGGCGTGAGCCACCGCGCCTGGCCACATCTG A G ZNF527 Ensembl:ENSG00000189164 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs980284033 Functional Loss SNV dbSNP153 33..33 33 - - - 26444 RMVar_ID_26444 Human_SNP_ID_664986326 A-to-I Human chr19 + 37392413 37392412 37392414 TTTTTATTTTATTTATTTATTTTTTTTGAGACAGGGTCTCACTCTGTTATCCAGGCTGGAATGCG TTTTTATTTTATTTATTTATTTTTTTTGAGAC__GGTCTCACTCTGTTATCCAGGCTGGAATGCG CAG C ZNF527 Ensembl:ENSG00000189164 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1225833715 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_6756173 26445 RMVar_ID_26445 Human_SNP_ID_664986329 A-to-I Human chr19 + 37392421 37392421 37392421 TTATTTATTTATTTTTTTTGAGACAGGGTCTCACTCTGTTATCCAGGCTGGAATGCGGTGACACA TTATTTATTTATTTTTTTTGAGACAGGGTCTCGCTCTGTTATCCAGGCTGGAATGCGGTGACACA A G ZNF527 Ensembl:ENSG00000189164 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs932781534 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1999848 26446 RMVar_ID_26446 Human_SNP_ID_664986330 A-to-I Human chr19 + 37392421 37392421 37392421 TTATTTATTTATTTTTTTTGAGACAGGGTCTCACTCTGTTATCCAGGCTGGAATGCGGTGACACA TTATTTATTTATTTTTTTTGAGACAGGGTCTCTCTCTGTTATCCAGGCTGGAATGCGGTGACACA A T ZNF527 Ensembl:ENSG00000189164 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs932781534 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1999848 26447 RMVar_ID_26447 Human_SNP_ID_665019698 A-to-I Human chr19 + 37538114 37538114 37538114 TTTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGGTCTCGATCTCCTGA TTTTTTTGTATTTTTAGTAGAGACGGGGTTTCCCCGTGTTAGCCAGGATGGTCTCGATCTCCTGA A C ZNF793 Ensembl:ENSG00000188227 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1366052947 Functional Loss SNV dbSNP153 33..33 33 - - - 26448 RMVar_ID_26448 Human_SNP_ID_665019711 A-to-I Human chr19 + 37538122 37538122 37538122 TATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGGTCTCGATCTCCTGACCTTGTGA TATTTTTAGTAGAGACGGGGTTTCACCGTGTTGGCCAGGATGGTCTCGATCTCCTGACCTTGTGA A G ZNF793 Ensembl:ENSG00000188227 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs372744419 Functional Loss SNV dbSNP153 33..33 33 - - - 26449 RMVar_ID_26449 Human_SNP_ID_665019712 A-to-I Human chr19 + 37538122 37538122 37538122 TATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGGTCTCGATCTCCTGACCTTGTGA TATTTTTAGTAGAGACGGGGTTTCACCGTGTTTGCCAGGATGGTCTCGATCTCCTGACCTTGTGA A T ZNF793 Ensembl:ENSG00000188227 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs372744419 Functional Loss SNV dbSNP153 33..33 33 - - - 26450 RMVar_ID_26450 Human_SNP_ID_665019941 A-to-I Human chr19 + 37538581 37538581 37538581 CCCCGCCCTTGGCCTCCCAAAGTGTTGGGATTACAGGCATGAGCCAACGCGCCCAACCGACAGTG CCCCGCCCTTGGCCTCCCAAAGTGTTGGGATTTCAGGCATGAGCCAACGCGCCCAACCGACAGTG A T ZNF793 Ensembl:ENSG00000188227 Protein coding 3'UTR GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1045458343 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1399595 26451 RMVar_ID_26451 Human_SNP_ID_665020293 A-to-I Human chr19 + 37540119 37540119 37540119 GAAACCCCATCTCTACTAAAAATACAAAAATTAGCCGGGTGTGGTGGCACACACCTGTAGTCCCA GAAACCCCATCTCTACTAAAAATACAAAAATTGGCCGGGTGTGGTGGCACACACCTGTAGTCCCA A G ZNF793 Ensembl:ENSG00000188227 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1406077941 Functional Loss SNV dbSNP153 33..33 33 - - - 26452 RMVar_ID_26452 Human_SNP_ID_665035267 A-to-I Human chr19 + 37603063 37603063 37603063 GAGTTTTGCTCTTGTTGCCTAGGCTGCAGTGCAATGGCATGATCTCGGCTCACTGCAACCTCCAC GAGTTTTGCTCTTGTTGCCTAGGCTGCAGTGCGATGGCATGATCTCGGCTCACTGCAACCTCCAC A G ZNF540 Ensembl:ENSG00000171817 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs989075169 Functional Loss SNV dbSNP153 33..33 33 - - - 26453 RMVar_ID_26453 Human_SNP_ID_665042594 A-to-I Human chr19 - 37632978 37632978 37632978 TTAGTAGAGATGGGGTTTCACCATGTTGGCCAAGCTGGTCTCAACTCCTGACCTCAGGTGATCCA TTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTCAACTCCTGACCTCAGGTGATCCA T C ZFP30 Ensembl:ENSG00000120784 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1568375826 Functional Loss SNV dbSNP153 33..33 33 - - - 26454 RMVar_ID_26454 Human_SNP_ID_665042634 A-to-I Human chr19 - 37633108 37633108 37633108 GGCGTGCAGTGGCACAGTCTCGGCTCACTGCAAGCTCTGCCTCCCGGGTTCAAGCCATTCTCCTC GGCGTGCAGTGGCACAGTCTCGGCTCACTGCAGGCTCTGCCTCCCGGGTTCAAGCCATTCTCCTC T C ZFP30 Ensembl:ENSG00000120784 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348115391 Functional Loss SNV dbSNP153 33..33 33 - - - 26455 RMVar_ID_26455 Human_SNP_ID_665042741 A-to-I Human chr19 - 37633446 37633446 37633446 GGGCAGCTGAGACAGGAGAATCACTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCCGAGATCACG GGGCAGCTGAGACAGGAGAATCACTTGAACCCCGGAGGCAGAGGTTGCAGTGAGCCGAGATCACG T G ZFP30 Ensembl:ENSG00000120784 Protein coding intron GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs1230892738 Functional Loss SNV dbSNP153 33..33 33 - - - 26456 RMVar_ID_26456 Human_SNP_ID_665042770 A-to-I Human chr19 - 37633547 37633547 37633547 GAGTTCGAGACCAGCCTGACCATCATGGTGAAACCTCATCTCCACTAAAAATACAAAAATTAGCC GAGTTCGAGACCAGCCTGACCATCATGGTGAAGCCTCATCTCCACTAAAAATACAAAAATTAGCC T C ZFP30 Ensembl:ENSG00000120784 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1008532570 Functional Loss SNV dbSNP153 33..33 33 - - - 26457 RMVar_ID_26457 Human_SNP_ID_665057254 A-to-I Human chr19 - 37693544 37693544 37693544 AATGGGGGCAAGATGGTTTACATCTCAAACGCACAAGTGTTGGACAACTGGAGTCAGTCTCCATG AATGGGGGCAAGATGGTTTACATCTCAAACGCGCAAGTGTTGGACAACTGGAGTCAGTCTCCATG T C SELENOKP1,AC093227.2 Ensembl:ENSG00000267319,Ensembl:ENSG00000267552 Pseudogene,Protein coding exon,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1263432217 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6797476 RMVar_hsa_circ_9422 26458 RMVar_ID_26458 Human_SNP_ID_665057256 A-to-I Human chr19 - 37693550 37693550 37693550 GCAGGGAATGGGGGCAAGATGGTTTACATCTCAAACGCACAAGTGTTGGACAACTGGAGTCAGTC GCAGGGAATGGGGGCAAGATGGTTTACATCTCGAACGCACAAGTGTTGGACAACTGGAGTCAGTC T C SELENOKP1,AC093227.2 Ensembl:ENSG00000267319,Ensembl:ENSG00000267552 Pseudogene,Protein coding exon,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs878964240 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6797476 RMVar_hsa_circ_9422 26459 RMVar_ID_26459 Human_SNP_ID_665059881 A-to-I Human chr19 - 37703235 37703235 37703235 TTATTTAAATTTACCTGTTGGTGGGGTGTGGTAGCTCACGCCTGTAATCTCATCACTCTGGGAGG TTATTTAAATTTACCTGTTGGTGGGGTGTGGTGGCTCACGCCTGTAATCTCATCACTCTGGGAGG T C AC093227.2,ZNF607 Ensembl:ENSG00000267552,Ensembl:ENSG00000198182 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941914286 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9422,RMVar_hsa_circ_297028,RMVar_hsa_circ_194503 26460 RMVar_ID_26460 Human_SNP_ID_665059882 A-to-I Human chr19 - 37703235 37703235 37703235 TTATTTAAATTTACCTGTTGGTGGGGTGTGGTAGCTCACGCCTGTAATCTCATCACTCTGGGAGG TTATTTAAATTTACCTGTTGGTGGGGTGTGGTCGCTCACGCCTGTAATCTCATCACTCTGGGAGG T G AC093227.2,ZNF607 Ensembl:ENSG00000267552,Ensembl:ENSG00000198182 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941914286 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9422,RMVar_hsa_circ_297028,RMVar_hsa_circ_194503 26461 RMVar_ID_26461 Human_SNP_ID_665060603 A-to-I Human chr19 - 37706188 37706188 37706188 TCTCTTCTCCTCTCTTTTCCATCTTTCGAGATAGAGTCTTGCTCTGTTGCCCAGGCTGGAGAAAA TCTCTTCTCCTCTCTTTTCCATCTTTCGAGATGGAGTCTTGCTCTGTTGCCCAGGCTGGAGAAAA T C AC093227.2,ZNF607 Ensembl:ENSG00000267552,Ensembl:ENSG00000198182 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs919763699 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18946791,Human_RBP_ID_20387098 RMVar_hsa_circ_9422,RMVar_hsa_circ_297028,RMVar_hsa_circ_194503 26462 RMVar_ID_26462 Human_SNP_ID_665060985 A-to-I Human chr19 - 37707642 37707642 37707642 TGAGGTGATCCACCACAGTAGCTGGGACCACAAGTGCATACCACCACACCTGGCTAATTTTTTTT TGAGGTGATCCACCACAGTAGCTGGGACCACAGGTGCATACCACCACACCTGGCTAATTTTTTTT T C AC093227.2,ZNF607 Ensembl:ENSG00000267552,Ensembl:ENSG00000198182 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1359650348 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9422,RMVar_hsa_circ_33291,RMVar_hsa_circ_297028,RMVar_hsa_circ_194503 26463 RMVar_ID_26463 Human_SNP_ID_665062978 A-to-I Human chr19 - 37715424 37715424 37715424 TTTTGTATTTTTAGTAGAGATGGGGTTTTACCATGTTGGTCAGGCTGGTCTTGAACTCAGATGAT TTTTGTATTTTTAGTAGAGATGGGGTTTTACCTTGTTGGTCAGGCTGGTCTTGAACTCAGATGAT T A AC093227.2,ZNF607 Ensembl:ENSG00000267552,Ensembl:ENSG00000198182 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1024007409 Functional Loss SNV dbSNP153 33..33 33 - - - 26464 RMVar_ID_26464 Human_SNP_ID_665062979 A-to-I Human chr19 - 37715424 37715424 37715424 TTTTGTATTTTTAGTAGAGATGGGGTTTTACCATGTTGGTCAGGCTGGTCTTGAACTCAGATGAT TTTTGTATTTTTAGTAGAGATGGGGTTTTACCGTGTTGGTCAGGCTGGTCTTGAACTCAGATGAT T C AC093227.2,ZNF607 Ensembl:ENSG00000267552,Ensembl:ENSG00000198182 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1024007409 Functional Loss SNV dbSNP153 33..33 33 - - - 26465 RMVar_ID_26465 Human_SNP_ID_665063031 A-to-I Human chr19 - 37715591 37715591 37715591 TCATCTTTTTTTTTTTTTTTAGATGGAGTTTCATTCTGTGGCCCAGGCTGGAGTGCAATGGCATG TCATCTTTTTTTTTTTTTTTAGATGGAGTTTCGTTCTGTGGCCCAGGCTGGAGTGCAATGGCATG T C AC093227.2,ZNF607 Ensembl:ENSG00000267552,Ensembl:ENSG00000198182 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1171390824 Functional Loss SNV dbSNP153 33..33 33 - - - 26466 RMVar_ID_26466 Human_SNP_ID_665067075 A-to-I Human chr19 - 37733757 37733757 37733757 TACTCGGAGGGCTGAGACACGAGAATCACTTGAACCCAGGAGGCGGAGGTTGCAGTGGGCCGAGA TACTCGGAGGGCTGAGACACGAGAATCACTTGTACCCAGGAGGCGGAGGTTGCAGTGGGCCGAGA T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1363164591 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13447001 26467 RMVar_ID_26467 Human_SNP_ID_665067077 A-to-I Human chr19 - 37733762 37733762 37733762 CCAGCTACTCGGAGGGCTGAGACACGAGAATCACTTGAACCCAGGAGGCGGAGGTTGCAGTGGGC CCAGCTACTCGGAGGGCTGAGACACGAGAATCGCTTGAACCCAGGAGGCGGAGGTTGCAGTGGGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1272285531 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13447001,Human_RBP_ID_25412190 26468 RMVar_ID_26468 Human_SNP_ID_665077662 A-to-I Human chr19 - 37777677 37777677 37777677 GGAGTGCAGTGGCGCAGTCTCGGTTCACTGCAACCTCTGCCTCCTGAGTTCAAGCAATTCCCCTG GGAGTGCAGTGGCGCAGTCTCGGTTCACTGCACCCTCTGCCTCCTGAGTTCAAGCAATTCCCCTG T G ZNF573 Ensembl:ENSG00000189144 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1046605735 Functional Loss SNV dbSNP153 33..33 33 - - - 26469 RMVar_ID_26469 Human_SNP_ID_665081081 A-to-I Human chr19 - 37791734 37791734 37791734 GCTGTTCCTCCTAACCGAATCCTGCCATGAACACAGCAGACACCGACTTCAGAATCAGGGTTCAC GCTGTTCCTCCTAACCGAATCCTGCCATGAACGCAGCAGACACCGACTTCAGAATCAGGGTTCAC T C ZNF573 Ensembl:ENSG00000189144 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1191459897 Functional Loss SNV dbSNP153 33..33 33 - - - 26470 RMVar_ID_26470 Human_SNP_ID_665081083 A-to-I Human chr19 - 37791740 37791740 37791740 TGCTGTGCTGTTCCTCCTAACCGAATCCTGCCATGAACACAGCAGACACCGACTTCAGAATCAGG TGCTGTGCTGTTCCTCCTAACCGAATCCTGCCGTGAACACAGCAGACACCGACTTCAGAATCAGG T C ZNF573 Ensembl:ENSG00000189144 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs984391227 Functional Loss SNV dbSNP153 33..33 33 - - - 26471 RMVar_ID_26471 Human_SNP_ID_665081121 A-to-I Human chr19 + 37791866 37791866 37791866 CCTTGAACTATTGGAGGAAAAAAAAAAAAAACAGAACTGGCCCAGAAAGCAAGGAAGGAGATTGC CCTTGAACTATTGGAGGAAAAAAAAAAAAAACGGAACTGGCCCAGAAAGCAAGGAAGGAGATTGC A G AC016582.2 Ensembl:ENSG00000267422 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1433956530 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5586181 Human_miRNA_ID_1877418,Human_miRNA_ID_1879030 26472 RMVar_ID_26472 Human_SNP_ID_665081283 A-to-I Human chr19 + 37792613 37792613 37792613 TATCCATCTCAGATACCAGCAACTCCCCCATCATATGAATCTGTAGATGACATTAATGCTGATAA TATCCATCTCAGATACCAGCAACTCCCCCATCGTATGAATCTGTAGATGACATTAATGCTGATAA A G AC016582.2 Ensembl:ENSG00000267422 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879202738 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23796028 26473 RMVar_ID_26473 Human_SNP_ID_665110027 A-to-I Human chr19 + 37912684 37912684 37912684 CACCCAGCTAATTTTTAAATTTTTGTAGAGATAGGGTCTCACACTATGTTGCCTAGACTGGTCTC CACCCAGCTAATTTTTAAATTTTTGTAGAGATGGGGTCTCACACTATGTTGCCTAGACTGGTCTC A G SIPA1L3 Ensembl:ENSG00000105738 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs918990752 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13447263 RMVar_hsa_circ_89034,RMVar_hsa_circ_194517 26474 RMVar_ID_26474 Human_SNP_ID_665110212 A-to-I Human chr19 + 37913489 37913489 37913489 ACAATCTCAGCTCACTGCAACCACTGCCTCCCAAGTTCAAGCCCATCTCCTGCCTCAGGCTCCTG ACAATCTCAGCTCACTGCAACCACTGCCTCCCGAGTTCAAGCCCATCTCCTGCCTCAGGCTCCTG A G SIPA1L3 Ensembl:ENSG00000105738 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1358056900 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89034,RMVar_hsa_circ_194517 26475 RMVar_ID_26475 Human_SNP_ID_665110228 A-to-I Human chr19 + 37913579 37913579 37913579 CACTATGCCCTGCTGATTTTTGTATTTTTAGTAGAGGAGGGGTTTTGCCATGTTAGCCAGGCTGG CACTATGCCCTGCTGATTTTTGTATTTTTAGTGGAGGAGGGGTTTTGCCATGTTAGCCAGGCTGG A G SIPA1L3 Ensembl:ENSG00000105738 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1231436606 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89034,RMVar_hsa_circ_194517 26476 RMVar_ID_26476 Human_SNP_ID_665110739 A-to-I Human chr19 + 37915634 37915611 37915635 CAACTCCTCACCTCAAGTGATCCGACGGCCTCAGCCTCCCAAAGTGTTGAGATTACAGATGTGAG CAACTCCTCA________________________CCTCCCAAAGTGTTGAGATTACAGATGTGAG ACCTCAAGTGATCCGACGGCCTCAG A SIPA1L3 Ensembl:ENSG00000105738 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167996103 Functional Loss DEL dbSNP153 11..34 33 - - - RMVar_hsa_circ_89034,RMVar_hsa_circ_194517 26477 RMVar_ID_26477 Human_SNP_ID_665110855 A-to-I Human chr19 + 37916156 37916156 37916156 TCAAATGACTGTCCTGCCTTAGCCTCCACAGTAGCTGGGATTACAGGCGCCCACCACCACACCCG TCAAATGACTGTCCTGCCTTAGCCTCCACAGTCGCTGGGATTACAGGCGCCCACCACCACACCCG A C SIPA1L3 Ensembl:ENSG00000105738 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1321010427 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89034,RMVar_hsa_circ_194517 26478 RMVar_ID_26478 Human_SNP_ID_665110917 A-to-I Human chr19 + 37916373 37916373 37916373 AATTTTTAAATTAGCCAGGCTTGGTGATGTGCACCTATAATCCCAGCTACTCAGGAGGCTGAGGT AATTTTTAAATTAGCCAGGCTTGGTGATGTGCTCCTATAATCCCAGCTACTCAGGAGGCTGAGGT A T SIPA1L3 Ensembl:ENSG00000105738 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1269753296 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89034,RMVar_hsa_circ_194517 26479 RMVar_ID_26479 Human_SNP_ID_665110920 A-to-I Human chr19 + 37916377 37916377 37916377 TTTAAATTAGCCAGGCTTGGTGATGTGCACCTATAATCCCAGCTACTCAGGAGGCTGAGGTGAGA TTTAAATTAGCCAGGCTTGGTGATGTGCACCTCTAATCCCAGCTACTCAGGAGGCTGAGGTGAGA A C SIPA1L3 Ensembl:ENSG00000105738 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1265176439 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89034,RMVar_hsa_circ_194517 26480 RMVar_ID_26480 Human_SNP_ID_665111032 A-to-I Human chr19 + 37916799 37916799 37916799 CTAGCCAACATGGTGAAATCCCATCTCTACTTAAAATACAAAAATTAGCTGAGTCTGGTGGCATG CTAGCCAACATGGTGAAATCCCATCTCTACTTGAAATACAAAAATTAGCTGAGTCTGGTGGCATG A G SIPA1L3 Ensembl:ENSG00000105738 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1230729569 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89034,RMVar_hsa_circ_194517 26481 RMVar_ID_26481 Human_SNP_ID_665112187 A-to-I Human chr19 + 37921726 37921726 37921726 GGGCTCAAGTGATCCTCCCACCTCAGCCTCCCAAGTAGCTGGGACCACAGGCATACGCCACCACG GGGCTCAAGTGATCCTCCCACCTCAGCCTCCCGAGTAGCTGGGACCACAGGCATACGCCACCACG A G SIPA1L3 Ensembl:ENSG00000105738 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1320262559 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89034,RMVar_hsa_circ_194517 26482 RMVar_ID_26482 Human_SNP_ID_665112203 A-to-I Human chr19 + 37921803 37921803 37921803 TTTTTTTATTTTTGTGGAAACAGGTTCTTGCTATGTTGTCGTGGCTGGTCTCGAACTCCTGGCCT TTTTTTTATTTTTGTGGAAACAGGTTCTTGCTGTGTTGTCGTGGCTGGTCTCGAACTCCTGGCCT A G SIPA1L3 Ensembl:ENSG00000105738 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs943691506 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13447339 RMVar_hsa_circ_89034,RMVar_hsa_circ_194517 26483 RMVar_ID_26483 Human_SNP_ID_665121362 A-to-I Human chr19 + 37957811 37957811 37957811 CACAGCTCACTGCAGCCTCGACTTCTGAGCTCAAGTGATCCTCTCACCTTAGCTTCTGGAGTAGC CACAGCTCACTGCAGCCTCGACTTCTGAGCTCTAGTGATCCTCTCACCTTAGCTTCTGGAGTAGC A T SIPA1L3 Ensembl:ENSG00000105738 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1359386389 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89034,RMVar_hsa_circ_194517 26484 RMVar_ID_26484 Human_SNP_ID_665128227 A-to-I Human chr19 + 37985443 37985443 37985443 CCAGCTACCGGGGAGGCTGAGACAGGAGGATCACTTGAAGCCAGGAGTTCAAAACCAGCCTAGAC CCAGCTACCGGGGAGGCTGAGACAGGAGGATCGCTTGAAGCCAGGAGTTCAAAACCAGCCTAGAC A G SIPA1L3 Ensembl:ENSG00000105738 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1418129737 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89034,RMVar_hsa_circ_194517 26485 RMVar_ID_26485 Human_SNP_ID_665156312 A-to-I Human chr19 + 38097832 38097832 38097832 TGCCCACCTCGGCCTCTCAAAGTGCTGGGATTACAGGTGTGAGCCACTGTGTCTGGCCTGTATAC TGCCCACCTCGGCCTCTCAAAGTGCTGGGATTGCAGGTGTGAGCCACTGTGTCTGGCCTGTATAC A G SIPA1L3 Ensembl:ENSG00000105738 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1238792983 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89034,RMVar_hsa_circ_194517,RMVar_hsa_circ_111884,RMVar_hsa_circ_328565,RMVar_hsa_circ_288005,RMVar_hsa_circ_83396,RMVar_hsa_circ_100903,RMVar_hsa_circ_79593,RMVar_hsa_circ_27117,RMVar_hsa_circ_194519,RMVar_hsa_circ_194521,RMVar_hsa_circ_194522,RMVar_hsa_circ_194520,RMVar_hsa_circ_50172,RMVar_hsa_circ_373900,RMVar_hsa_circ_194523 26486 RMVar_ID_26486 Human_SNP_ID_665157605 A-to-I Human chr19 + 38102378 38102378 38102378 ATTATTATTTTTTATAGAGACAAGGTCTTGCTATGTTACCCAGACTGGTCTCAAACACAAGGCCT ATTATTATTTTTTATAGAGACAAGGTCTTGCTGTGTTACCCAGACTGGTCTCAAACACAAGGCCT A G SIPA1L3 Ensembl:ENSG00000105738 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs572428501 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16910,RMVar_hsa_circ_89034,RMVar_hsa_circ_194517,RMVar_hsa_circ_111884,RMVar_hsa_circ_328565,RMVar_hsa_circ_83396,RMVar_hsa_circ_100903,RMVar_hsa_circ_79593,RMVar_hsa_circ_27117,RMVar_hsa_circ_194519,RMVar_hsa_circ_194521,RMVar_hsa_circ_194522,RMVar_hsa_circ_194520,RMVar_hsa_circ_373900,RMVar_hsa_circ_78151,RMVar_hsa_circ_194523,RMVar_hsa_circ_371875,RMVar_hsa_circ_105140,RMVar_hsa_circ_56687,RMVar_hsa_circ_79932,RMVar_hsa_circ_194525,RMVar_hsa_circ_194526,RMVar_hsa_circ_194527,RMVar_hsa_circ_194528 26487 RMVar_ID_26487 Human_SNP_ID_665158187 A-to-I Human chr19 + 38104593 38104593 38104593 AGTATTGGTTTTTTTGTTTTTTTGTTTTTTTGAGACAGTCTCGCTCTGTCACCCAGGCTGGAGTG AGTATTGGTTTTTTTGTTTTTTTGTTTTTTTGCGACAGTCTCGCTCTGTCACCCAGGCTGGAGTG A C SIPA1L3 Ensembl:ENSG00000105738 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs890662894 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16910,RMVar_hsa_circ_89034,RMVar_hsa_circ_194517,RMVar_hsa_circ_111884,RMVar_hsa_circ_328565,RMVar_hsa_circ_83396,RMVar_hsa_circ_100903,RMVar_hsa_circ_79593,RMVar_hsa_circ_27117,RMVar_hsa_circ_194519,RMVar_hsa_circ_194521,RMVar_hsa_circ_194522,RMVar_hsa_circ_194520,RMVar_hsa_circ_373900,RMVar_hsa_circ_78151,RMVar_hsa_circ_194523,RMVar_hsa_circ_371875,RMVar_hsa_circ_105140,RMVar_hsa_circ_56687,RMVar_hsa_circ_79932,RMVar_hsa_circ_194525,RMVar_hsa_circ_194526,RMVar_hsa_circ_194527,RMVar_hsa_circ_194528 26488 RMVar_ID_26488 Human_SNP_ID_665158199 A-to-I Human chr19 + 38104630 38104630 38104630 GTCTCGCTCTGTCACCCAGGCTGGAGTGCATTAGAACGATCTTGGCTCACTGCAACCTTCACCTC GTCTCGCTCTGTCACCCAGGCTGGAGTGCATTGGAACGATCTTGGCTCACTGCAACCTTCACCTC A G SIPA1L3 Ensembl:ENSG00000105738 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs968239887 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16910,RMVar_hsa_circ_89034,RMVar_hsa_circ_194517,RMVar_hsa_circ_111884,RMVar_hsa_circ_328565,RMVar_hsa_circ_83396,RMVar_hsa_circ_100903,RMVar_hsa_circ_79593,RMVar_hsa_circ_27117,RMVar_hsa_circ_194519,RMVar_hsa_circ_194521,RMVar_hsa_circ_194522,RMVar_hsa_circ_194520,RMVar_hsa_circ_373900,RMVar_hsa_circ_78151,RMVar_hsa_circ_194523,RMVar_hsa_circ_371875,RMVar_hsa_circ_105140,RMVar_hsa_circ_56687,RMVar_hsa_circ_79932,RMVar_hsa_circ_194525,RMVar_hsa_circ_194526,RMVar_hsa_circ_194527,RMVar_hsa_circ_194528 26489 RMVar_ID_26489 Human_SNP_ID_665161775 A-to-I Human chr19 + 38118314 38118314 38118314 AGGCGTGGTGGTGGGCGCCTGTAATCCCAGCTACTGGGGAGGCAGAGACAGGAGAATCGCCTGAA AGGCGTGGTGGTGGGCGCCTGTAATCCCAGCTCCTGGGGAGGCAGAGACAGGAGAATCGCCTGAA A C SIPA1L3 Ensembl:ENSG00000105738 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1249599147 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89034,RMVar_hsa_circ_194517,RMVar_hsa_circ_111884,RMVar_hsa_circ_83396,RMVar_hsa_circ_100903,RMVar_hsa_circ_79593,RMVar_hsa_circ_27117,RMVar_hsa_circ_194519,RMVar_hsa_circ_194521,RMVar_hsa_circ_194522,RMVar_hsa_circ_194520,RMVar_hsa_circ_78151,RMVar_hsa_circ_105140,RMVar_hsa_circ_56687,RMVar_hsa_circ_39807,RMVar_hsa_circ_194526,RMVar_hsa_circ_194527,RMVar_hsa_circ_295386,RMVar_hsa_circ_362752,RMVar_hsa_circ_47214,RMVar_hsa_circ_5608,RMVar_hsa_circ_30752,RMVar_hsa_circ_98955,RMVar_hsa_circ_194529,RMVar_hsa_circ_370045,RMVar_hsa_circ_30815,RMVar_hsa_circ_194530,RMVar_hsa_circ_194531 26490 RMVar_ID_26490 Human_SNP_ID_665161956 A-to-I Human chr19 + 38118939 38118939 38118939 GAAACTGGCCGCGTGTGGTGGCTCACAGCTGTAATCCCAACACTTTGGGAAGCCCAGGAGGTAGG GAAACTGGCCGCGTGTGGTGGCTCACAGCTGTTATCCCAACACTTTGGGAAGCCCAGGAGGTAGG A T SIPA1L3 Ensembl:ENSG00000105738 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1229970692 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89034,RMVar_hsa_circ_194517,RMVar_hsa_circ_111884,RMVar_hsa_circ_83396,RMVar_hsa_circ_100903,RMVar_hsa_circ_79593,RMVar_hsa_circ_27117,RMVar_hsa_circ_194519,RMVar_hsa_circ_194521,RMVar_hsa_circ_194522,RMVar_hsa_circ_194520,RMVar_hsa_circ_78151,RMVar_hsa_circ_105140,RMVar_hsa_circ_56687,RMVar_hsa_circ_39807,RMVar_hsa_circ_194526,RMVar_hsa_circ_194527,RMVar_hsa_circ_295386,RMVar_hsa_circ_362752,RMVar_hsa_circ_47214,RMVar_hsa_circ_5608,RMVar_hsa_circ_30752,RMVar_hsa_circ_98955,RMVar_hsa_circ_194529,RMVar_hsa_circ_370045,RMVar_hsa_circ_30815,RMVar_hsa_circ_194530,RMVar_hsa_circ_194531 26491 RMVar_ID_26491 Human_SNP_ID_665164385 A-to-I Human chr19 + 38126716 38126716 38126716 GCACCACCATGCCCAGCTAATTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGCCCAGGC GCACCACCATGCCCAGCTAATTTTGTATTTTTGGTAGAGACGGGGTTTCACCATGTTGCCCAGGC A G SIPA1L3 Ensembl:ENSG00000105738 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1479604992 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89034,RMVar_hsa_circ_194517,RMVar_hsa_circ_83396,RMVar_hsa_circ_100903,RMVar_hsa_circ_79593,RMVar_hsa_circ_27117,RMVar_hsa_circ_194519,RMVar_hsa_circ_194521,RMVar_hsa_circ_194520,RMVar_hsa_circ_78151,RMVar_hsa_circ_105140,RMVar_hsa_circ_194533,RMVar_hsa_circ_39807,RMVar_hsa_circ_194526,RMVar_hsa_circ_194527,RMVar_hsa_circ_362752,RMVar_hsa_circ_47214,RMVar_hsa_circ_5608,RMVar_hsa_circ_30752,RMVar_hsa_circ_98955,RMVar_hsa_circ_30815,RMVar_hsa_circ_104164,RMVar_hsa_circ_194531,RMVar_hsa_circ_328751,RMVar_hsa_circ_349157,RMVar_hsa_circ_120894,RMVar_hsa_circ_194535,RMVar_hsa_circ_87100,RMVar_hsa_circ_194534,RMVar_hsa_circ_194532 26492 RMVar_ID_26492 Human_SNP_ID_665164472 A-to-I Human chr19 + 38127041 38127041 38127041 ATGGAGAAACCCCGTCTCTACTAAAAATACAAAATTAGCTGGGTGTGGTGGCGCATGCCTGTGAT ATGGAGAAACCCCGTCTCTACTAAAAATACAATATTAGCTGGGTGTGGTGGCGCATGCCTGTGAT A T SIPA1L3 Ensembl:ENSG00000105738 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1488546965 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89034,RMVar_hsa_circ_194517,RMVar_hsa_circ_83396,RMVar_hsa_circ_100903,RMVar_hsa_circ_79593,RMVar_hsa_circ_27117,RMVar_hsa_circ_194519,RMVar_hsa_circ_194521,RMVar_hsa_circ_194520,RMVar_hsa_circ_78151,RMVar_hsa_circ_105140,RMVar_hsa_circ_194533,RMVar_hsa_circ_39807,RMVar_hsa_circ_194526,RMVar_hsa_circ_194527,RMVar_hsa_circ_362752,RMVar_hsa_circ_47214,RMVar_hsa_circ_5608,RMVar_hsa_circ_30752,RMVar_hsa_circ_98955,RMVar_hsa_circ_30815,RMVar_hsa_circ_104164,RMVar_hsa_circ_194531,RMVar_hsa_circ_328751,RMVar_hsa_circ_349157,RMVar_hsa_circ_120894,RMVar_hsa_circ_194535,RMVar_hsa_circ_87100,RMVar_hsa_circ_194534,RMVar_hsa_circ_194532 26493 RMVar_ID_26493 Human_SNP_ID_665165890 A-to-I Human chr19 + 38131973 38131973 38131973 TTCGTAGTGTCAACTATCTAGACTGGGTTCACACCTGTAATCGTAACACTCTGGGAGGCTGAGGT TTCGTAGTGTCAACTATCTAGACTGGGTTCACTCCTGTAATCGTAACACTCTGGGAGGCTGAGGT A T SIPA1L3 Ensembl:ENSG00000105738 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1423209212 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89034,RMVar_hsa_circ_194517,RMVar_hsa_circ_100903,RMVar_hsa_circ_79593,RMVar_hsa_circ_194519,RMVar_hsa_circ_194520,RMVar_hsa_circ_78151,RMVar_hsa_circ_105140,RMVar_hsa_circ_194533,RMVar_hsa_circ_39807,RMVar_hsa_circ_194526,RMVar_hsa_circ_194527,RMVar_hsa_circ_47214,RMVar_hsa_circ_5608,RMVar_hsa_circ_30752,RMVar_hsa_circ_98955,RMVar_hsa_circ_30815,RMVar_hsa_circ_104164,RMVar_hsa_circ_194531,RMVar_hsa_circ_349157,RMVar_hsa_circ_120894,RMVar_hsa_circ_87100,RMVar_hsa_circ_194534,RMVar_hsa_circ_17616,RMVar_hsa_circ_311657,RMVar_hsa_circ_194532,RMVar_hsa_circ_292039,RMVar_hsa_circ_194537,RMVar_hsa_circ_194538 26494 RMVar_ID_26494 Human_SNP_ID_665166113 A-to-I Human chr19 + 38132711 38132711 38132711 GCTCTGTCACCCAGGCTGGAGTGCAGTGGCGCAATCTTGGCTCACTGCAACCTCCGCCTCCTGGG GCTCTGTCACCCAGGCTGGAGTGCAGTGGCGCTATCTTGGCTCACTGCAACCTCCGCCTCCTGGG A T SIPA1L3 Ensembl:ENSG00000105738 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1478705822 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89034,RMVar_hsa_circ_194517,RMVar_hsa_circ_100903,RMVar_hsa_circ_79593,RMVar_hsa_circ_194519,RMVar_hsa_circ_194520,RMVar_hsa_circ_78151,RMVar_hsa_circ_105140,RMVar_hsa_circ_194533,RMVar_hsa_circ_39807,RMVar_hsa_circ_194526,RMVar_hsa_circ_194527,RMVar_hsa_circ_47214,RMVar_hsa_circ_5608,RMVar_hsa_circ_30752,RMVar_hsa_circ_98955,RMVar_hsa_circ_30815,RMVar_hsa_circ_104164,RMVar_hsa_circ_194531,RMVar_hsa_circ_349157,RMVar_hsa_circ_120894,RMVar_hsa_circ_87100,RMVar_hsa_circ_194534,RMVar_hsa_circ_17616,RMVar_hsa_circ_311657,RMVar_hsa_circ_194532,RMVar_hsa_circ_292039,RMVar_hsa_circ_194537,RMVar_hsa_circ_194538 26495 RMVar_ID_26495 Human_SNP_ID_665166129 A-to-I Human chr19 + 38132765 38132765 38132765 CGCCTCCTGGGTTCCAGCGATTCTCCTGTGTCAGCCTCCTGAGTAGCTGGGATTACAGGCATGTA CGCCTCCTGGGTTCCAGCGATTCTCCTGTGTCGGCCTCCTGAGTAGCTGGGATTACAGGCATGTA A G SIPA1L3 Ensembl:ENSG00000105738 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1013427684 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89034,RMVar_hsa_circ_194517,RMVar_hsa_circ_100903,RMVar_hsa_circ_79593,RMVar_hsa_circ_194519,RMVar_hsa_circ_194520,RMVar_hsa_circ_78151,RMVar_hsa_circ_105140,RMVar_hsa_circ_194533,RMVar_hsa_circ_39807,RMVar_hsa_circ_194526,RMVar_hsa_circ_194527,RMVar_hsa_circ_47214,RMVar_hsa_circ_5608,RMVar_hsa_circ_30752,RMVar_hsa_circ_98955,RMVar_hsa_circ_30815,RMVar_hsa_circ_104164,RMVar_hsa_circ_194531,RMVar_hsa_circ_349157,RMVar_hsa_circ_120894,RMVar_hsa_circ_87100,RMVar_hsa_circ_194534,RMVar_hsa_circ_17616,RMVar_hsa_circ_311657,RMVar_hsa_circ_194532,RMVar_hsa_circ_292039,RMVar_hsa_circ_194537,RMVar_hsa_circ_194538 26496 RMVar_ID_26496 Human_SNP_ID_665166146 A-to-I Human chr19 + 38132831 38132831 38132831 CACCACACCTGGCTAAATTTCATATTTTTAGTAGAGCTGGGGTTTCACCATGTTGGCCAGGCTGG CACCACACCTGGCTAAATTTCATATTTTTAGTGGAGCTGGGGTTTCACCATGTTGGCCAGGCTGG A G SIPA1L3 Ensembl:ENSG00000105738 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs766610205 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89034,RMVar_hsa_circ_194517,RMVar_hsa_circ_100903,RMVar_hsa_circ_79593,RMVar_hsa_circ_194519,RMVar_hsa_circ_194520,RMVar_hsa_circ_78151,RMVar_hsa_circ_105140,RMVar_hsa_circ_194533,RMVar_hsa_circ_39807,RMVar_hsa_circ_194526,RMVar_hsa_circ_194527,RMVar_hsa_circ_47214,RMVar_hsa_circ_5608,RMVar_hsa_circ_30752,RMVar_hsa_circ_98955,RMVar_hsa_circ_30815,RMVar_hsa_circ_104164,RMVar_hsa_circ_194531,RMVar_hsa_circ_349157,RMVar_hsa_circ_120894,RMVar_hsa_circ_87100,RMVar_hsa_circ_194534,RMVar_hsa_circ_17616,RMVar_hsa_circ_311657,RMVar_hsa_circ_194532,RMVar_hsa_circ_292039,RMVar_hsa_circ_194537,RMVar_hsa_circ_194538 26497 RMVar_ID_26497 Human_SNP_ID_665166593 A-to-I Human chr19 + 38134622 38134622 38134622 CCAGCTATTCAGGAGGCTGAGGCAGAAGAATCACTTGAACCCAGGAGGCAGAGTTTGCAGTGAGC CCAGCTATTCAGGAGGCTGAGGCAGAAGAATCGCTTGAACCCAGGAGGCAGAGTTTGCAGTGAGC A G SIPA1L3 Ensembl:ENSG00000105738 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1468123123 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89034,RMVar_hsa_circ_194517,RMVar_hsa_circ_100903,RMVar_hsa_circ_79593,RMVar_hsa_circ_194519,RMVar_hsa_circ_194520,RMVar_hsa_circ_78151,RMVar_hsa_circ_105140,RMVar_hsa_circ_194533,RMVar_hsa_circ_39807,RMVar_hsa_circ_194526,RMVar_hsa_circ_194527,RMVar_hsa_circ_47214,RMVar_hsa_circ_5608,RMVar_hsa_circ_30752,RMVar_hsa_circ_98955,RMVar_hsa_circ_30815,RMVar_hsa_circ_104164,RMVar_hsa_circ_194531,RMVar_hsa_circ_349157,RMVar_hsa_circ_120894,RMVar_hsa_circ_87100,RMVar_hsa_circ_194534,RMVar_hsa_circ_17616,RMVar_hsa_circ_311657,RMVar_hsa_circ_194532,RMVar_hsa_circ_292039,RMVar_hsa_circ_194537,RMVar_hsa_circ_194538 26498 RMVar_ID_26498 Human_SNP_ID_665167072 A-to-I Human chr19 + 38136346 38136346 38136346 AATTCAAGGGCCAGACGCAGTGGCTCACACCTATAATCCCAGCACTTTGGGAGGCCGAGGGAGGC AATTCAAGGGCCAGACGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGGAGGC A G SIPA1L3 Ensembl:ENSG00000105738 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs912350524 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89034,RMVar_hsa_circ_194517,RMVar_hsa_circ_100903,RMVar_hsa_circ_79593,RMVar_hsa_circ_194519,RMVar_hsa_circ_194520,RMVar_hsa_circ_78151,RMVar_hsa_circ_105140,RMVar_hsa_circ_194533,RMVar_hsa_circ_39807,RMVar_hsa_circ_194526,RMVar_hsa_circ_194527,RMVar_hsa_circ_47214,RMVar_hsa_circ_5608,RMVar_hsa_circ_30752,RMVar_hsa_circ_98955,RMVar_hsa_circ_30815,RMVar_hsa_circ_104164,RMVar_hsa_circ_194531,RMVar_hsa_circ_349157,RMVar_hsa_circ_120894,RMVar_hsa_circ_87100,RMVar_hsa_circ_194534,RMVar_hsa_circ_17616,RMVar_hsa_circ_311657,RMVar_hsa_circ_194532,RMVar_hsa_circ_292039,RMVar_hsa_circ_194537,RMVar_hsa_circ_194538 26499 RMVar_ID_26499 Human_SNP_ID_665167113 A-to-I Human chr19 + 38136493 38136493 38136493 GGGCATGGTGGCAGGCGCCTGTAATCCCAGCTACTCAAGAGGCTGAGGCAGGAGAATCACTTGAA GGGCATGGTGGCAGGCGCCTGTAATCCCAGCTGCTCAAGAGGCTGAGGCAGGAGAATCACTTGAA A G SIPA1L3 Ensembl:ENSG00000105738 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1002277606 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89034,RMVar_hsa_circ_194517,RMVar_hsa_circ_100903,RMVar_hsa_circ_79593,RMVar_hsa_circ_194519,RMVar_hsa_circ_194520,RMVar_hsa_circ_78151,RMVar_hsa_circ_105140,RMVar_hsa_circ_194533,RMVar_hsa_circ_39807,RMVar_hsa_circ_194526,RMVar_hsa_circ_194527,RMVar_hsa_circ_47214,RMVar_hsa_circ_5608,RMVar_hsa_circ_30752,RMVar_hsa_circ_98955,RMVar_hsa_circ_30815,RMVar_hsa_circ_104164,RMVar_hsa_circ_194531,RMVar_hsa_circ_349157,RMVar_hsa_circ_120894,RMVar_hsa_circ_87100,RMVar_hsa_circ_194534,RMVar_hsa_circ_17616,RMVar_hsa_circ_311657,RMVar_hsa_circ_194532,RMVar_hsa_circ_292039,RMVar_hsa_circ_194537,RMVar_hsa_circ_194538 26500 RMVar_ID_26500 Human_SNP_ID_665167305 A-to-I Human chr19 + 38137288 38137288 38137288 TCAGCTCACTGCAACCTCCGCTTCCCAGGTTCAAGCGATCCTCCTGCCTCAACCCCCCTAGTAGC TCAGCTCACTGCAACCTCCGCTTCCCAGGTTCGAGCGATCCTCCTGCCTCAACCCCCCTAGTAGC A G SIPA1L3 Ensembl:ENSG00000105738 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1396739766 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89034,RMVar_hsa_circ_194517,RMVar_hsa_circ_100903,RMVar_hsa_circ_79593,RMVar_hsa_circ_194519,RMVar_hsa_circ_194520,RMVar_hsa_circ_78151,RMVar_hsa_circ_105140,RMVar_hsa_circ_194533,RMVar_hsa_circ_39807,RMVar_hsa_circ_194526,RMVar_hsa_circ_194527,RMVar_hsa_circ_47214,RMVar_hsa_circ_5608,RMVar_hsa_circ_30752,RMVar_hsa_circ_98955,RMVar_hsa_circ_30815,RMVar_hsa_circ_104164,RMVar_hsa_circ_194531,RMVar_hsa_circ_349157,RMVar_hsa_circ_120894,RMVar_hsa_circ_87100,RMVar_hsa_circ_194534,RMVar_hsa_circ_17616,RMVar_hsa_circ_311657,RMVar_hsa_circ_194532,RMVar_hsa_circ_292039,RMVar_hsa_circ_194537,RMVar_hsa_circ_194538 26501 RMVar_ID_26501 Human_SNP_ID_665170336 A-to-I Human chr19 + 38149300 38149300 38149300 GCGTGTGCCTGTCTTCCCTTGGGAGGCTGAGGAAAGAGAATATCGCTTGAACCCTGGAAGTGGAA GCGTGTGCCTGTCTTCCCTTGGGAGGCTGAGGCAAGAGAATATCGCTTGAACCCTGGAAGTGGAA A C SIPA1L3 Ensembl:ENSG00000105738 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs8109695 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89034,RMVar_hsa_circ_194517,RMVar_hsa_circ_100903,RMVar_hsa_circ_194519,RMVar_hsa_circ_78151,RMVar_hsa_circ_105140,RMVar_hsa_circ_194533,RMVar_hsa_circ_39807,RMVar_hsa_circ_194526,RMVar_hsa_circ_194527,RMVar_hsa_circ_5608,RMVar_hsa_circ_30752,RMVar_hsa_circ_98955,RMVar_hsa_circ_104164,RMVar_hsa_circ_194531,RMVar_hsa_circ_120894,RMVar_hsa_circ_87100,RMVar_hsa_circ_194534,RMVar_hsa_circ_112006,RMVar_hsa_circ_122128,RMVar_hsa_circ_17616,RMVar_hsa_circ_311657,RMVar_hsa_circ_194532,RMVar_hsa_circ_194538,RMVar_hsa_circ_333358,RMVar_hsa_circ_353707,RMVar_hsa_circ_362881,RMVar_hsa_circ_194541,RMVar_hsa_circ_194542,RMVar_hsa_circ_194540,RMVar_hsa_circ_122454,RMVar_hsa_circ_87871,RMVar_hsa_circ_106617,RMVar_hsa_circ_194544,RMVar_hsa_circ_194546,RMVar_hsa_circ_194545,RMVar_hsa_circ_194543 26502 RMVar_ID_26502 Human_SNP_ID_665170337 A-to-I Human chr19 + 38149300 38149300 38149300 GCGTGTGCCTGTCTTCCCTTGGGAGGCTGAGGAAAGAGAATATCGCTTGAACCCTGGAAGTGGAA GCGTGTGCCTGTCTTCCCTTGGGAGGCTGAGGGAAGAGAATATCGCTTGAACCCTGGAAGTGGAA A G SIPA1L3 Ensembl:ENSG00000105738 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs8109695 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89034,RMVar_hsa_circ_194517,RMVar_hsa_circ_100903,RMVar_hsa_circ_194519,RMVar_hsa_circ_78151,RMVar_hsa_circ_105140,RMVar_hsa_circ_194533,RMVar_hsa_circ_39807,RMVar_hsa_circ_194526,RMVar_hsa_circ_194527,RMVar_hsa_circ_5608,RMVar_hsa_circ_30752,RMVar_hsa_circ_98955,RMVar_hsa_circ_104164,RMVar_hsa_circ_194531,RMVar_hsa_circ_120894,RMVar_hsa_circ_87100,RMVar_hsa_circ_194534,RMVar_hsa_circ_112006,RMVar_hsa_circ_122128,RMVar_hsa_circ_17616,RMVar_hsa_circ_311657,RMVar_hsa_circ_194532,RMVar_hsa_circ_194538,RMVar_hsa_circ_333358,RMVar_hsa_circ_353707,RMVar_hsa_circ_362881,RMVar_hsa_circ_194541,RMVar_hsa_circ_194542,RMVar_hsa_circ_194540,RMVar_hsa_circ_122454,RMVar_hsa_circ_87871,RMVar_hsa_circ_106617,RMVar_hsa_circ_194544,RMVar_hsa_circ_194546,RMVar_hsa_circ_194545,RMVar_hsa_circ_194543 26503 RMVar_ID_26503 Human_SNP_ID_665170867 A-to-I Human chr19 + 38151601 38151598 38151601 CAACCTCAGACAGGGAGAAGACCTTCTACCACAACCGGCTGTGATCCAAGGAGGACTGGACGTTA CAACCTCAGACAGGGAGAAGACCTTCTACC___ACCGGCTGTGATCCAAGGAGGACTGGACGTTA CACA C SIPA1L3 Ensembl:ENSG00000105738 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1045480040 Functional Loss DEL dbSNP153 31..33 33 - - - RMVar_hsa_circ_89034,RMVar_hsa_circ_194517,RMVar_hsa_circ_100903,RMVar_hsa_circ_194519,RMVar_hsa_circ_78151,RMVar_hsa_circ_105140,RMVar_hsa_circ_194533,RMVar_hsa_circ_39807,RMVar_hsa_circ_194526,RMVar_hsa_circ_194527,RMVar_hsa_circ_5608,RMVar_hsa_circ_30752,RMVar_hsa_circ_98955,RMVar_hsa_circ_104164,RMVar_hsa_circ_194531,RMVar_hsa_circ_120894,RMVar_hsa_circ_87100,RMVar_hsa_circ_194534,RMVar_hsa_circ_112006,RMVar_hsa_circ_122128,RMVar_hsa_circ_17616,RMVar_hsa_circ_311657,RMVar_hsa_circ_194532,RMVar_hsa_circ_194538,RMVar_hsa_circ_333358,RMVar_hsa_circ_353707,RMVar_hsa_circ_362881,RMVar_hsa_circ_194541,RMVar_hsa_circ_194542,RMVar_hsa_circ_194540,RMVar_hsa_circ_122454,RMVar_hsa_circ_87871,RMVar_hsa_circ_106617,RMVar_hsa_circ_194544,RMVar_hsa_circ_194546,RMVar_hsa_circ_194545,RMVar_hsa_circ_194543 26504 RMVar_ID_26504 Human_SNP_ID_665170870 A-to-I Human chr19 + 38151601 38151601 38151601 CAACCTCAGACAGGGAGAAGACCTTCTACCACAACCGGCTGTGATCCAAGGAGGACTGGACGTTA CAACCTCAGACAGGGAGAAGACCTTCTACCACGACCGGCTGTGATCCAAGGAGGACTGGACGTTA A G SIPA1L3 Ensembl:ENSG00000105738 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs332845 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2625 RMVar_hsa_circ_89034,RMVar_hsa_circ_194517,RMVar_hsa_circ_100903,RMVar_hsa_circ_194519,RMVar_hsa_circ_78151,RMVar_hsa_circ_105140,RMVar_hsa_circ_194533,RMVar_hsa_circ_39807,RMVar_hsa_circ_194526,RMVar_hsa_circ_194527,RMVar_hsa_circ_5608,RMVar_hsa_circ_30752,RMVar_hsa_circ_98955,RMVar_hsa_circ_104164,RMVar_hsa_circ_194531,RMVar_hsa_circ_120894,RMVar_hsa_circ_87100,RMVar_hsa_circ_194534,RMVar_hsa_circ_112006,RMVar_hsa_circ_122128,RMVar_hsa_circ_17616,RMVar_hsa_circ_311657,RMVar_hsa_circ_194532,RMVar_hsa_circ_194538,RMVar_hsa_circ_333358,RMVar_hsa_circ_353707,RMVar_hsa_circ_362881,RMVar_hsa_circ_194541,RMVar_hsa_circ_194542,RMVar_hsa_circ_194540,RMVar_hsa_circ_122454,RMVar_hsa_circ_87871,RMVar_hsa_circ_106617,RMVar_hsa_circ_194544,RMVar_hsa_circ_194546,RMVar_hsa_circ_194545,RMVar_hsa_circ_194543 26505 RMVar_ID_26505 Human_SNP_ID_665170871 A-to-I Human chr19 + 38151601 38151601 38151601 CAACCTCAGACAGGGAGAAGACCTTCTACCACAACCGGCTGTGATCCAAGGAGGACTGGACGTTA CAACCTCAGACAGGGAGAAGACCTTCTACCACTACCGGCTGTGATCCAAGGAGGACTGGACGTTA A T SIPA1L3 Ensembl:ENSG00000105738 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs332845 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2625 RMVar_hsa_circ_89034,RMVar_hsa_circ_194517,RMVar_hsa_circ_100903,RMVar_hsa_circ_194519,RMVar_hsa_circ_78151,RMVar_hsa_circ_105140,RMVar_hsa_circ_194533,RMVar_hsa_circ_39807,RMVar_hsa_circ_194526,RMVar_hsa_circ_194527,RMVar_hsa_circ_5608,RMVar_hsa_circ_30752,RMVar_hsa_circ_98955,RMVar_hsa_circ_104164,RMVar_hsa_circ_194531,RMVar_hsa_circ_120894,RMVar_hsa_circ_87100,RMVar_hsa_circ_194534,RMVar_hsa_circ_112006,RMVar_hsa_circ_122128,RMVar_hsa_circ_17616,RMVar_hsa_circ_311657,RMVar_hsa_circ_194532,RMVar_hsa_circ_194538,RMVar_hsa_circ_333358,RMVar_hsa_circ_353707,RMVar_hsa_circ_362881,RMVar_hsa_circ_194541,RMVar_hsa_circ_194542,RMVar_hsa_circ_194540,RMVar_hsa_circ_122454,RMVar_hsa_circ_87871,RMVar_hsa_circ_106617,RMVar_hsa_circ_194544,RMVar_hsa_circ_194546,RMVar_hsa_circ_194545,RMVar_hsa_circ_194543 26506 RMVar_ID_26506 Human_SNP_ID_665175150 A-to-I Human chr19 + 38167599 38167599 38167599 CTGTTTGTTTTTTAGAAACAGGGTCCTGCTCTATTGCCCAGGCTGGGGTGCAGTAGTACGACCAT CTGTTTGTTTTTTAGAAACAGGGTCCTGCTCTGTTGCCCAGGCTGGGGTGCAGTAGTACGACCAT A G SIPA1L3 Ensembl:ENSG00000105738 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs553341716 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_98955,RMVar_hsa_circ_194531,RMVar_hsa_circ_87100,RMVar_hsa_circ_112006,RMVar_hsa_circ_122128,RMVar_hsa_circ_194532,RMVar_hsa_circ_353707,RMVar_hsa_circ_194541,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 26507 RMVar_ID_26507 Human_SNP_ID_665175199 A-to-I Human chr19 + 38167773 38167773 38167773 TGTTAGTAGAGAAGGGGTCTCACTGTGTTGCCAAGGTTGGTCTCGAACTCCTGGGCTCAAGCGAT TGTTAGTAGAGAAGGGGTCTCACTGTGTTGCCCAGGTTGGTCTCGAACTCCTGGGCTCAAGCGAT A C SIPA1L3 Ensembl:ENSG00000105738 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1011515957 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_98955,RMVar_hsa_circ_194531,RMVar_hsa_circ_87100,RMVar_hsa_circ_112006,RMVar_hsa_circ_122128,RMVar_hsa_circ_194532,RMVar_hsa_circ_353707,RMVar_hsa_circ_194541,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 26508 RMVar_ID_26508 Human_SNP_ID_665177614 A-to-I Human chr19 + 38177395 38177395 38177395 AAAAAAAAAAAAAAATTCTAGTTTATTTTGCCAGGCGCAGTGACTCATGCCTGTAATCCCAGCTC AAAAAAAAAAAAAAATTCTAGTTTATTTTGCCGGGCGCAGTGACTCATGCCTGTAATCCCAGCTC A G SIPA1L3 Ensembl:ENSG00000105738 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1353420503 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_98955,RMVar_hsa_circ_194531,RMVar_hsa_circ_87100,RMVar_hsa_circ_112006,RMVar_hsa_circ_122128,RMVar_hsa_circ_194532,RMVar_hsa_circ_353707,RMVar_hsa_circ_194541,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 26509 RMVar_ID_26509 Human_SNP_ID_665208133 A-to-I Human chr19 + 38286636 38286636 38286636 CTCCGTCTCTACTCAAAATACAAAAAAAAATTAGCCGGGCCTGGTGGCGGGCGCCTGTGGTCCCA CTCCGTCTCTACTCAAAATACAAAAAAAAATTGGCCGGGCCTGGTGGCGGGCGCCTGTGGTCCCA A G SPINT2 Ensembl:ENSG00000167642 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348559151 Functional Loss SNV dbSNP153 33..33 33 - - - 26510 RMVar_ID_26510 Human_SNP_ID_665214249 A-to-I Human chr19 - 38307725 38307725 38307725 TGCAGGTTCTCCCCAGACCTCCTGGGGCTGCAAGCGAGCTCAGCCCTGGCCTGGCTGACCCTGGA TGCAGGTTCTCCCCAGACCTCCTGGGGCTGCAGGCGAGCTCAGCCCTGGCCTGGCTGACCCTGGA T C YIF1B Ensembl:ENSG00000167645 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs778660385 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4525697,Human_RBP_ID_17386808,Human_RBP_ID_22446670,Human_RBP_ID_22763367 Human_Splice_Rec_2001092,Human_Splice_Rec_2001106,Human_Splice_Rec_2001120,Human_Splice_Rec_2001134,Human_Splice_Rec_2001142,Human_Splice_Rec_2001150,Human_Splice_Rec_2001164,Human_Splice_Rec_2001178,Human_Splice_Rec_2001196,Human_Splice_Rec_2001204,Human_Splice_Rec_2001222,Human_Splice_Rec_2001232 RMVar_hsa_circ_30418,RMVar_hsa_circ_120770,RMVar_hsa_circ_38767,RMVar_hsa_circ_194555,RMVar_hsa_circ_46522 26511 RMVar_ID_26511 Human_SNP_ID_665220676 A-to-I Human chr19 + 38331442 38331442 38331442 GGTCAGGAGATCAAGACCATCCTGGCTAACACAGTGAAACCCGTCTCTACTAAAAATACAAAAAA GGTCAGGAGATCAAGACCATCCTGGCTAACACGGTGAAACCCGTCTCTACTAAAAATACAAAAAA A G KCNK6 Ensembl:ENSG00000099337 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1170025642 Functional Loss SNV dbSNP153 33..33 33 - - - 26512 RMVar_ID_26512 Human_SNP_ID_665222687 A-to-I Human chr19 + 38338422 38338422 38338422 CGCCCGCCTCGGCCTCCTAGAGTGCTGGGATTACAGGCGTGAGCCACCTCACCCGGCCTTGTTCC CGCCCGCCTCGGCCTCCTAGAGTGCTGGGATTGCAGGCGTGAGCCACCTCACCCGGCCTTGTTCC A G CATSPERG Ensembl:ENSG00000099338 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs550396016 Functional Loss SNV dbSNP153 33..33 33 - - - 26513 RMVar_ID_26513 Human_SNP_ID_665222761 A-to-I Human chr19 + 38338794 38338794 38338794 AAATGCTAAGGCAGGATCATCATAATGAGCCTAGGAGGTTGAGGCTGCAGGGAACTGTGATCATG AAATGCTAAGGCAGGATCATCATAATGAGCCTGGGAGGTTGAGGCTGCAGGGAACTGTGATCATG A G CATSPERG Ensembl:ENSG00000099338 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1034163720 Functional Loss SNV dbSNP153 33..33 33 - - - 26514 RMVar_ID_26514 Human_SNP_ID_665222762 A-to-I Human chr19 + 38338794 38338794 38338794 AAATGCTAAGGCAGGATCATCATAATGAGCCTAGGAGGTTGAGGCTGCAGGGAACTGTGATCATG AAATGCTAAGGCAGGATCATCATAATGAGCCTTGGAGGTTGAGGCTGCAGGGAACTGTGATCATG A T CATSPERG Ensembl:ENSG00000099338 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1034163720 Functional Loss SNV dbSNP153 33..33 33 - - - 26515 RMVar_ID_26515 Human_SNP_ID_665225294 A-to-I Human chr19 + 38347890 38347890 38347890 TTGAACCTGGGAGGCGGAAGTTGCAGTGAGCCAAGATCGTACCACTGTACTCCAGCCTGGGCGAT TTGAACCTGGGAGGCGGAAGTTGCAGTGAGCCGAGATCGTACCACTGTACTCCAGCCTGGGCGAT A G CATSPERG Ensembl:ENSG00000099338 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1195649066 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25413167 26516 RMVar_ID_26516 Human_SNP_ID_665225411 A-to-I Human chr19 + 38348395 38348395 38348395 GTTGCCCAGACTGGTCTTAAACTCCTGCCCTTAAGCAATCCTCCCATCTAGGCCTCCTAAAGTGC GTTGCCCAGACTGGTCTTAAACTCCTGCCCTTTAGCAATCCTCCCATCTAGGCCTCCTAAAGTGC A T CATSPERG Ensembl:ENSG00000099338 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1389867717 Functional Loss SNV dbSNP153 33..33 33 - - - 26517 RMVar_ID_26517 Human_SNP_ID_665234248 A-to-I Human chr19 + 38377723 38377723 38377723 TGGATCTCGGTGCACTGCAACCTCCGCCTCCCAGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCT TGGATCTCGGTGCACTGCAACCTCCGCCTCCCGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCT A G PSMD8 Ensembl:ENSG00000099341 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1359560208 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_194558,RMVar_hsa_circ_105002,RMVar_hsa_circ_327461,RMVar_hsa_circ_194559 26518 RMVar_ID_26518 Human_SNP_ID_665234345 A-to-I Human chr19 + 38378133 38378132 38378134 CCTGAAATCCCAGCACTTTGGGAGGCTGAGACAGGAGGATCACTTGAGCCCAAGATTTCCAGACC CCTGAAATCCCAGCACTTTGGGAGGCTGAGAC__GAGGATCACTTGAGCCCAAGATTTCCAGACC CAG C PSMD8 Ensembl:ENSG00000099341 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1203501238 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_194558,RMVar_hsa_circ_105002,RMVar_hsa_circ_327461,RMVar_hsa_circ_194559 26519 RMVar_ID_26519 Human_SNP_ID_665234528 A-to-I Human chr19 + 38378894 38378894 38378894 AGAATCGCTTGAACCCGGCAAGCGGAGGTTGCAGTGAGCCAAGAACGCACCATTGCACTCCAGCC AGAATCGCTTGAACCCGGCAAGCGGAGGTTGCGGTGAGCCAAGAACGCACCATTGCACTCCAGCC A G PSMD8 Ensembl:ENSG00000099341 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs927121826 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_194558,RMVar_hsa_circ_105002,RMVar_hsa_circ_327461,RMVar_hsa_circ_194559 26520 RMVar_ID_26520 Human_SNP_ID_665241118 A-to-I Human chr19 + 38400190 38400190 38400190 TTTGGCCAGGCTGGTCTCGAATTCCTGACCTCAAGTGATCCACCTGCCTTGGTCTCCCAAGTGAT TTTGGCCAGGCTGGTCTCGAATTCCTGACCTCCAGTGATCCACCTGCCTTGGTCTCCCAAGTGAT A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs999971524 Functional Loss SNV dbSNP153 33..33 33 - - - 26521 RMVar_ID_26521 Human_SNP_ID_665242837 A-to-I Human chr19 + 38406123 38406123 38406123 GTGATCTGCCTGTCTTGGCCTCCCAAAGTGCTAGGATTACAGGCATGAGCCACTGCACCCAGCCT GTGATCTGCCTGTCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGCACCCAGCCT A G FAM98C Ensembl:ENSG00000130244 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1016904712 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_375366,RMVar_hsa_circ_4905,RMVar_hsa_circ_194564,RMVar_hsa_circ_194565,RMVar_hsa_circ_78379 26522 RMVar_ID_26522 Human_SNP_ID_665242839 A-to-I Human chr19 + 38406129 38406129 38406129 TGCCTGTCTTGGCCTCCCAAAGTGCTAGGATTACAGGCATGAGCCACTGCACCCAGCCTTTTTTT TGCCTGTCTTGGCCTCCCAAAGTGCTAGGATTGCAGGCATGAGCCACTGCACCCAGCCTTTTTTT A G FAM98C Ensembl:ENSG00000130244 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1184267270 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_375366,RMVar_hsa_circ_4905,RMVar_hsa_circ_194564,RMVar_hsa_circ_194565,RMVar_hsa_circ_78379 26523 RMVar_ID_26523 Human_SNP_ID_665242951 A-to-I Human chr19 + 38406547 38406547 38406547 CCTGTTATCCCAGCACTTTGGGAGGCCAAGGCAAGAGGATCACTTGAGCTCAGAAGTTTGAGACC CCTGTTATCCCAGCACTTTGGGAGGCCAAGGCGAGAGGATCACTTGAGCTCAGAAGTTTGAGACC A G FAM98C Ensembl:ENSG00000130244 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1007487252 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_375366,RMVar_hsa_circ_4905,RMVar_hsa_circ_194564,RMVar_hsa_circ_194565,RMVar_hsa_circ_78379 26524 RMVar_ID_26524 Human_SNP_ID_665242980 A-to-I Human chr19 + 38406678 38406678 38406678 TGGTGGCGCATGCTTGTCCATCTCAGTTACTCAGGAGGCTAAGGTAGGAGGATCACTTGAGCCCA TGGTGGCGCATGCTTGTCCATCTCAGTTACTCGGGAGGCTAAGGTAGGAGGATCACTTGAGCCCA A G FAM98C Ensembl:ENSG00000130244 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs569544972 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_375366,RMVar_hsa_circ_4905,RMVar_hsa_circ_194564,RMVar_hsa_circ_194565,RMVar_hsa_circ_78379 26525 RMVar_ID_26525 Human_SNP_ID_665243244 A-to-I Human chr19 + 38407568 38407568 38407568 AATTTTTGTATCTTTAGTAGTGACGGGGTTTCACCATATTGGTCAGGCTGGTCTTGAACTCCTGA AATTTTTGTATCTTTAGTAGTGACGGGGTTTCGCCATATTGGTCAGGCTGGTCTTGAACTCCTGA A G FAM98C Ensembl:ENSG00000130244 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs957355013 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114987,RMVar_hsa_circ_194566 26526 RMVar_ID_26526 Human_SNP_ID_665243476 A-to-I Human chr19 + 38408381 38408381 38408381 AGAGATCGAGACCATCCTGGCTAACACGGTGAAACCCTGTCTCTACTAAAAATATAAAAAATTAG AGAGATCGAGACCATCCTGGCTAACACGGTGATACCCTGTCTCTACTAAAAATATAAAAAATTAG A T FAM98C Ensembl:ENSG00000130244 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs982451983 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114987,RMVar_hsa_circ_194566 26527 RMVar_ID_26527 Human_SNP_ID_665296704 A-to-I Human chr19 - 38589217 38589217 38589217 CTCACTGCAACCTCCTCCTCCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGG CTCACTGCAACCTCCTCCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGG T C MAP4K1 Ensembl:ENSG00000104814 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1460487376 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_137430 Human_Splice_Rec_2003030,Human_Splice_Rec_2003031 RMVar_hsa_circ_110942,RMVar_hsa_circ_127237,RMVar_hsa_circ_119332,RMVar_hsa_circ_122070,RMVar_hsa_circ_113157,RMVar_hsa_circ_194594,RMVar_hsa_circ_194598,RMVar_hsa_circ_83164,RMVar_hsa_circ_108197,RMVar_hsa_circ_194600,RMVar_hsa_circ_76391,RMVar_hsa_circ_194599,RMVar_hsa_circ_194596,RMVar_hsa_circ_194597,RMVar_hsa_circ_194595,RMVar_hsa_circ_99244,RMVar_hsa_circ_194593,RMVar_hsa_circ_194601 26528 RMVar_ID_26528 Human_SNP_ID_665296705 A-to-I Human chr19 - 38589217 38589217 38589217 CTCACTGCAACCTCCTCCTCCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGG CTCACTGCAACCTCCTCCTCCCAGGTTCAAGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGG T G MAP4K1 Ensembl:ENSG00000104814 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1460487376 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_137430 Human_Splice_Rec_2003030,Human_Splice_Rec_2003031 RMVar_hsa_circ_110942,RMVar_hsa_circ_127237,RMVar_hsa_circ_119332,RMVar_hsa_circ_122070,RMVar_hsa_circ_113157,RMVar_hsa_circ_194594,RMVar_hsa_circ_194598,RMVar_hsa_circ_83164,RMVar_hsa_circ_108197,RMVar_hsa_circ_194600,RMVar_hsa_circ_76391,RMVar_hsa_circ_194599,RMVar_hsa_circ_194596,RMVar_hsa_circ_194597,RMVar_hsa_circ_194595,RMVar_hsa_circ_99244,RMVar_hsa_circ_194593,RMVar_hsa_circ_194601 26529 RMVar_ID_26529 Human_SNP_ID_665296708 A-to-I Human chr19 - 38589227 38589227 38589227 ACGATCTCGCCTCACTGCAACCTCCTCCTCCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCG ACGATCTCGCCTCACTGCAACCTCCTCCTCCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCG T C MAP4K1 Ensembl:ENSG00000104814 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1392759708 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2003030,Human_Splice_Rec_2003031 RMVar_hsa_circ_110942,RMVar_hsa_circ_127237,RMVar_hsa_circ_119332,RMVar_hsa_circ_122070,RMVar_hsa_circ_113157,RMVar_hsa_circ_194594,RMVar_hsa_circ_194598,RMVar_hsa_circ_83164,RMVar_hsa_circ_108197,RMVar_hsa_circ_194600,RMVar_hsa_circ_76391,RMVar_hsa_circ_194599,RMVar_hsa_circ_194596,RMVar_hsa_circ_194597,RMVar_hsa_circ_194595,RMVar_hsa_circ_99244,RMVar_hsa_circ_194593,RMVar_hsa_circ_194601 26530 RMVar_ID_26530 Human_SNP_ID_665296723 A-to-I Human chr19 - 38589259 38589259 38589259 TCACTCTGTCCCCCAGGCTGGAGTGCAGTGGCACGATCTCGCCTCACTGCAACCTCCTCCTCCCA TCACTCTGTCCCCCAGGCTGGAGTGCAGTGGCGCGATCTCGCCTCACTGCAACCTCCTCCTCCCA T C MAP4K1 Ensembl:ENSG00000104814 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1205443820 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2003030,Human_Splice_Rec_2003031 RMVar_hsa_circ_110942,RMVar_hsa_circ_127237,RMVar_hsa_circ_119332,RMVar_hsa_circ_122070,RMVar_hsa_circ_113157,RMVar_hsa_circ_194594,RMVar_hsa_circ_194598,RMVar_hsa_circ_83164,RMVar_hsa_circ_108197,RMVar_hsa_circ_194600,RMVar_hsa_circ_76391,RMVar_hsa_circ_194599,RMVar_hsa_circ_194596,RMVar_hsa_circ_194597,RMVar_hsa_circ_194595,RMVar_hsa_circ_99244,RMVar_hsa_circ_194593,RMVar_hsa_circ_194601 26531 RMVar_ID_26531 Human_SNP_ID_665296883 A-to-I Human chr19 - 38589812 38589811 38589813 TTACTTAGCCTGGTCTGGAACTCCTGGACTCAAGAGATTCACCTGTGTAGGCTTCCCAAAGTGCT TTACTTAGCCTGGTCTGGAACTCCTGGACTC__GAGATTCACCTGTGTAGGCTTCCCAAAGTGCT CTT C MAP4K1 Ensembl:ENSG00000104814 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1282919479 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_110942,RMVar_hsa_circ_127237,RMVar_hsa_circ_119332,RMVar_hsa_circ_122070,RMVar_hsa_circ_113157,RMVar_hsa_circ_194594,RMVar_hsa_circ_194598,RMVar_hsa_circ_83164,RMVar_hsa_circ_108197,RMVar_hsa_circ_194600,RMVar_hsa_circ_76391,RMVar_hsa_circ_194599,RMVar_hsa_circ_194596,RMVar_hsa_circ_194597,RMVar_hsa_circ_194595,RMVar_hsa_circ_194593 26532 RMVar_ID_26532 Human_SNP_ID_665297872 A-to-I Human chr19 - 38592383 38592383 38592383 TTTAGTAGAGACGGGGTTTCGCCTTGTTAGCCAGGCTGGTCTCAAACTACTGACCTCAGGTGATC TTTAGTAGAGACGGGGTTTCGCCTTGTTAGCCTGGCTGGTCTCAAACTACTGACCTCAGGTGATC T A MAP4K1 Ensembl:ENSG00000104814 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1025266755 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110942,RMVar_hsa_circ_127237,RMVar_hsa_circ_119332,RMVar_hsa_circ_122070,RMVar_hsa_circ_113157,RMVar_hsa_circ_194594,RMVar_hsa_circ_194598,RMVar_hsa_circ_83164,RMVar_hsa_circ_108197,RMVar_hsa_circ_194600,RMVar_hsa_circ_76391,RMVar_hsa_circ_194599,RMVar_hsa_circ_194596,RMVar_hsa_circ_194597,RMVar_hsa_circ_194595,RMVar_hsa_circ_194593 26533 RMVar_ID_26533 Human_SNP_ID_665297874 A-to-I Human chr19 - 38592387 38592387 38592387 TATTTTTAGTAGAGACGGGGTTTCGCCTTGTTAGCCAGGCTGGTCTCAAACTACTGACCTCAGGT TATTTTTAGTAGAGACGGGGTTTCGCCTTGTTCGCCAGGCTGGTCTCAAACTACTGACCTCAGGT T G MAP4K1 Ensembl:ENSG00000104814 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs755650236 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110942,RMVar_hsa_circ_127237,RMVar_hsa_circ_119332,RMVar_hsa_circ_122070,RMVar_hsa_circ_113157,RMVar_hsa_circ_194594,RMVar_hsa_circ_194598,RMVar_hsa_circ_83164,RMVar_hsa_circ_108197,RMVar_hsa_circ_194600,RMVar_hsa_circ_76391,RMVar_hsa_circ_194599,RMVar_hsa_circ_194596,RMVar_hsa_circ_194597,RMVar_hsa_circ_194595,RMVar_hsa_circ_194593 26534 RMVar_ID_26534 Human_SNP_ID_665299713 A-to-I Human chr19 - 38598904 38598904 38598904 GGTTCAAGCGATTCTCCTGCCTCACCCTCCCAAGTAGCTGGGATTACAGGCACCTGCCACCACAC GGTTCAAGCGATTCTCCTGCCTCACCCTCCCAGGTAGCTGGGATTACAGGCACCTGCCACCACAC T C MAP4K1 Ensembl:ENSG00000104814 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1159263005 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75539,RMVar_hsa_circ_110942,RMVar_hsa_circ_127237,RMVar_hsa_circ_119332,RMVar_hsa_circ_122070,RMVar_hsa_circ_194594,RMVar_hsa_circ_194598,RMVar_hsa_circ_83164,RMVar_hsa_circ_108197,RMVar_hsa_circ_194596,RMVar_hsa_circ_194597,RMVar_hsa_circ_194595,RMVar_hsa_circ_194593,RMVar_hsa_circ_123536,RMVar_hsa_circ_99781,RMVar_hsa_circ_194602,RMVar_hsa_circ_194603,RMVar_hsa_circ_101880,RMVar_hsa_circ_194604,RMVar_hsa_circ_94292,RMVar_hsa_circ_194605,RMVar_hsa_circ_194606 26535 RMVar_ID_26535 Human_SNP_ID_665300597 A-to-I Human chr19 - 38602051 38602051 38602051 ACTGACAGCTGGGAGTGGTGCCTCACGCCTGTAATCTCAGCACTTTGGGAGGCTGAGGCAGGTGA ACTGACAGCTGGGAGTGGTGCCTCACGCCTGTTATCTCAGCACTTTGGGAGGCTGAGGCAGGTGA T A MAP4K1 Ensembl:ENSG00000104814 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1221812995 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110942,RMVar_hsa_circ_127237,RMVar_hsa_circ_119332,RMVar_hsa_circ_122070,RMVar_hsa_circ_194594,RMVar_hsa_circ_83164,RMVar_hsa_circ_194596,RMVar_hsa_circ_194597,RMVar_hsa_circ_194595,RMVar_hsa_circ_194593,RMVar_hsa_circ_111900,RMVar_hsa_circ_94292,RMVar_hsa_circ_194606,RMVar_hsa_circ_376145,RMVar_hsa_circ_194608,RMVar_hsa_circ_110693,RMVar_hsa_circ_194609,RMVar_hsa_circ_194607 26536 RMVar_ID_26536 Human_SNP_ID_665303408 A-to-I Human chr19 - 38609246 38609246 38609246 CCTGTAGTCCAAGCTACTTGGGAGGCTGAGGTAGGAGGATTGCCTGAACCTGGGAGGTGGAGGTT CCTGTAGTCCAAGCTACTTGGGAGGCTGAGGTGGGAGGATTGCCTGAACCTGGGAGGTGGAGGTT T C MAP4K1 Ensembl:ENSG00000104814 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1408564722 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127237,RMVar_hsa_circ_119332,RMVar_hsa_circ_122070,RMVar_hsa_circ_194594,RMVar_hsa_circ_83164,RMVar_hsa_circ_194596,RMVar_hsa_circ_194595,RMVar_hsa_circ_194593,RMVar_hsa_circ_94292,RMVar_hsa_circ_194606,RMVar_hsa_circ_110693,RMVar_hsa_circ_94392,RMVar_hsa_circ_194607,RMVar_hsa_circ_194612 26537 RMVar_ID_26537 Human_SNP_ID_665304860 A-to-I Human chr19 - 38614664 38614664 38614664 CACCCACCTTGGCCTCCCAAAGTGCTGGGATTATAGGCATGAGCCACTGCGCCAGGCCTATTGGC CACCCACCTTGGCCTCCCAAAGTGCTGGGATTGTAGGCATGAGCCACTGCGCCAGGCCTATTGGC T C MAP4K1 Ensembl:ENSG00000104814 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1371539625 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25413317 RMVar_hsa_circ_127237,RMVar_hsa_circ_194594,RMVar_hsa_circ_83164,RMVar_hsa_circ_194593,RMVar_hsa_circ_119627,RMVar_hsa_circ_194617 26538 RMVar_ID_26538 Human_SNP_ID_665308060 A-to-I Human chr19 + 38626382 38626382 38626382 CGTTGATCAGAAGTCCTCCAGTGGCTGGGTGTAGTGACTCACCCCCGTGATTCCAGTACTTGTGG CGTTGATCAGAAGTCCTCCAGTGGCTGGGTGTGGTGACTCACCCCCGTGATTCCAGTACTTGTGG A G EIF3K Ensembl:ENSG00000178982 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985356319 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13448684 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 26539 RMVar_ID_26539 Human_SNP_ID_665308166 A-to-I Human chr19 + 38626860 38626860 38626860 ATGGAGTCTCACGCCATTGCCTAGGCTGTAGTACAGTGGCACGATCTTGGCTCACTGCAACCTCT ATGGAGTCTCACGCCATTGCCTAGGCTGTAGTGCAGTGGCACGATCTTGGCTCACTGCAACCTCT A G EIF3K Ensembl:ENSG00000178982 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1382752601 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13448704 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 26540 RMVar_ID_26540 Human_SNP_ID_665308587 A-to-I Human chr19 + 38628654 38628654 38628654 CGAGACCAGCCTGACCAACGTGGAGAAACCCCATCTCTACTAAAAATACAAAGTTGGCCGGGCGT CGAGACCAGCCTGACCAACGTGGAGAAACCCCGTCTCTACTAAAAATACAAAGTTGGCCGGGCGT A G EIF3K Ensembl:ENSG00000178982 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1172462798 Functional Loss SNV dbSNP153 33..33 33 - - - 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 26541 RMVar_ID_26541 Human_SNP_ID_665308590 A-to-I Human chr19 + 38628663 38628663 38628663 CCTGACCAACGTGGAGAAACCCCATCTCTACTAAAAATACAAAGTTGGCCGGGCGTGGTGGCGCA CCTGACCAACGTGGAGAAACCCCATCTCTACTGAAAATACAAAGTTGGCCGGGCGTGGTGGCGCA A G EIF3K Ensembl:ENSG00000178982 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978851864 Functional Loss SNV dbSNP153 33..33 33 - - - 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 26542 RMVar_ID_26542 Human_SNP_ID_665308592 A-to-I Human chr19 + 38628671 38628671 38628671 ACGTGGAGAAACCCCATCTCTACTAAAAATACAAAGTTGGCCGGGCGTGGTGGCGCATGCCTGTA ACGTGGAGAAACCCCATCTCTACTAAAAATACCAAGTTGGCCGGGCGTGGTGGCGCATGCCTGTA A C EIF3K Ensembl:ENSG00000178982 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1385198645 Functional Loss SNV dbSNP153 33..33 33 - - - 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 26543 RMVar_ID_26543 Human_SNP_ID_665308824 A-to-I Human chr19 + 38629412 38629412 38629412 GACCTCCCAGGCTCAAGTGATCCCCGCACTTCAGCCTCCTGAGTAGCTGGGACTAACAGGCCCAC GACCTCCCAGGCTCAAGTGATCCCCGCACTTCGGCCTCCTGAGTAGCTGGGACTAACAGGCCCAC A G EIF3K Ensembl:ENSG00000178982 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946167684 Functional Loss SNV dbSNP153 33..33 33 - - - 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 26544 RMVar_ID_26544 Human_SNP_ID_665309006 A-to-I Human chr19 + 38630209 38630209 38630209 GGAGTATGGCTCTGTCGCCCAGGCTAGAGTGCAGTGATATGATCTTGGCTCGCTGCAACCTCTGC GGAGTATGGCTCTGTCGCCCAGGCTAGAGTGCCGTGATATGATCTTGGCTCGCTGCAACCTCTGC A C EIF3K Ensembl:ENSG00000178982 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs977709292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_521150 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 26545 RMVar_ID_26545 Human_SNP_ID_665309007 A-to-I Human chr19 + 38630209 38630209 38630209 GGAGTATGGCTCTGTCGCCCAGGCTAGAGTGCAGTGATATGATCTTGGCTCGCTGCAACCTCTGC GGAGTATGGCTCTGTCGCCCAGGCTAGAGTGCGGTGATATGATCTTGGCTCGCTGCAACCTCTGC A G EIF3K Ensembl:ENSG00000178982 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs977709292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_521150 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 26546 RMVar_ID_26546 Human_SNP_ID_665309010 A-to-I Human chr19 + 38630215 38630215 38630215 TGGCTCTGTCGCCCAGGCTAGAGTGCAGTGATATGATCTTGGCTCGCTGCAACCTCTGCCTCCCA TGGCTCTGTCGCCCAGGCTAGAGTGCAGTGATGTGATCTTGGCTCGCTGCAACCTCTGCCTCCCA A G EIF3K Ensembl:ENSG00000178982 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1032070091 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17924016 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 26547 RMVar_ID_26547 Human_SNP_ID_665309022 A-to-I Human chr19 + 38630247 38630247 38630247 ATGATCTTGGCTCGCTGCAACCTCTGCCTCCCAGGTTCAAGTGATTCTTCTGCCTCATCTTCCCA ATGATCTTGGCTCGCTGCAACCTCTGCCTCCCGGGTTCAAGTGATTCTTCTGCCTCATCTTCCCA A G EIF3K Ensembl:ENSG00000178982 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs921482477 Functional Loss SNV dbSNP153 33..33 33 - - - 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 26548 RMVar_ID_26548 Human_SNP_ID_665309210 A-to-I Human chr19 + 38630700 38630700 38630700 TTGTTGTTTTTTGTTTTGTTTTGTTTTGAGACAGAGCCTCCCTCTGTCGCCCAGTCTGGAATGCA TTGTTGTTTTTTGTTTTGTTTTGTTTTGAGACGGAGCCTCCCTCTGTCGCCCAGTCTGGAATGCA A G EIF3K Ensembl:ENSG00000178982 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1221082962 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2564934,Human_RBP_ID_13448839,Human_RBP_ID_23177570 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 26549 RMVar_ID_26549 Human_SNP_ID_665309281 A-to-I Human chr19 + 38631000 38631000 38631000 GCCTGGCTGATTTCTTTATTTTTAGTAGAGACAGGGTTTCACCCTGTTGGCCAGGGTAGTCTCGA GCCTGGCTGATTTCTTTATTTTTAGTAGAGACGGGGTTTCACCCTGTTGGCCAGGGTAGTCTCGA A G EIF3K Ensembl:ENSG00000178982 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1449035027 Functional Loss SNV dbSNP153 33..33 33 - - - 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 26550 RMVar_ID_26550 Human_SNP_ID_665309292 A-to-I Human chr19 + 38631025 38631025 38631025 TAGAGACAGGGTTTCACCCTGTTGGCCAGGGTAGTCTCGAACTCCTGACCTCAAGTGATCCACCC TAGAGACAGGGTTTCACCCTGTTGGCCAGGGTCGTCTCGAACTCCTGACCTCAAGTGATCCACCC A C EIF3K Ensembl:ENSG00000178982 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs538323347 Functional Loss SNV dbSNP153 33..33 33 - - - 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 26551 RMVar_ID_26551 Human_SNP_ID_665309293 A-to-I Human chr19 + 38631025 38631025 38631025 TAGAGACAGGGTTTCACCCTGTTGGCCAGGGTAGTCTCGAACTCCTGACCTCAAGTGATCCACCC TAGAGACAGGGTTTCACCCTGTTGGCCAGGGTGGTCTCGAACTCCTGACCTCAAGTGATCCACCC A G EIF3K Ensembl:ENSG00000178982 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs538323347 Functional Loss SNV dbSNP153 33..33 33 - - - 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 26552 RMVar_ID_26552 Human_SNP_ID_665309311 A-to-I Human chr19 + 38631071 38631071 38631071 GACCTCAAGTGATCCACCCACCTCAGCCTCCCAAAGTGCTGGGATTATAGGTGTGAGCCACCACA GACCTCAAGTGATCCACCCACCTCAGCCTCCCGAAGTGCTGGGATTATAGGTGTGAGCCACCACA A G EIF3K Ensembl:ENSG00000178982 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs991843009 Functional Loss SNV dbSNP153 33..33 33 - - - 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 26553 RMVar_ID_26553 Human_SNP_ID_665309665 A-to-I Human chr19 + 38632166 38632166 38632166 GGCTGGGAGTGGTGGCTCACCCCTGTAATCCCAACGCTTTGAGAGGCCAGCGTGGGCAGATCACT GGCTGGGAGTGGTGGCTCACCCCTGTAATCCCGACGCTTTGAGAGGCCAGCGTGGGCAGATCACT A G EIF3K Ensembl:ENSG00000178982 Protein coding intron GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,29796672,31158229 RNA-Seq:(High) rs1333330146 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8839315 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 26554 RMVar_ID_26554 Human_SNP_ID_665309676 A-to-I Human chr19 + 38632191 38632191 38632191 TAATCCCAACGCTTTGAGAGGCCAGCGTGGGCAGATCACTTGAGCCCAGGAGTTTGAGATCAGCC TAATCCCAACGCTTTGAGAGGCCAGCGTGGGCGGATCACTTGAGCCCAGGAGTTTGAGATCAGCC A G EIF3K Ensembl:ENSG00000178982 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1136574 Functional Loss SNV dbSNP153 33..33 33 - - - 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 26555 RMVar_ID_26555 Human_SNP_ID_665310163 A-to-I Human chr19 + 38633763 38633763 38633763 ATACCAGTGAGGGAGGCAGATCACGTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGGGA ATACCAGTGAGGGAGGCAGATCACGTGAGGTCGGGAGTTCGAGACCAGCCTGGCCAACATGGGGA A G EIF3K Ensembl:ENSG00000178982 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs926480537 Functional Loss SNV dbSNP153 33..33 33 - - - 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_194632,RMVar_hsa_circ_92925,RMVar_hsa_circ_194633 26556 RMVar_ID_26556 Human_SNP_ID_665310196 A-to-I Human chr19 + 38633862 38633862 38633862 GGACGTGTTGGCATGTGCCTGTAATCCCAGCTATTCGGGAGGCTGAGGCAGGAGAACCGCTTGAG GGACGTGTTGGCATGTGCCTGTAATCCCAGCTGTTCGGGAGGCTGAGGCAGGAGAACCGCTTGAG A G EIF3K Ensembl:ENSG00000178982 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1284646561 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25413474 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_194632,RMVar_hsa_circ_92925,RMVar_hsa_circ_194633 26557 RMVar_ID_26557 Human_SNP_ID_665310224 A-to-I Human chr19 + 38633964 38633964 38633964 ACTGCATTCCACTCTGGGCACTTTTAGTAGAGAAGGAGTTTGACCATGTTGGCCAGGCTGGTCTT ACTGCATTCCACTCTGGGCACTTTTAGTAGAGGAGGAGTTTGACCATGTTGGCCAGGCTGGTCTT A G EIF3K Ensembl:ENSG00000178982 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1454909876 Functional Loss SNV dbSNP153 33..33 33 - - - 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_194632,RMVar_hsa_circ_92925,RMVar_hsa_circ_194633 26558 RMVar_ID_26558 Human_SNP_ID_665310313 A-to-I Human chr19 + 38634236 38634236 38634236 CTCCTGCCTCAGCCTTCCAAATAGCTGAGACTATAGGCCTCTGCCACCTCGCCCAGCTAATTTTT CTCCTGCCTCAGCCTTCCAAATAGCTGAGACTGTAGGCCTCTGCCACCTCGCCCAGCTAATTTTT A G EIF3K Ensembl:ENSG00000178982 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1245474315 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25413482 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_194632,RMVar_hsa_circ_92925,RMVar_hsa_circ_194633 26559 RMVar_ID_26559 Human_SNP_ID_665310941 A-to-I Human chr19 + 38636410 38636410 38636410 GAGGCTGAGGCAGGAGAATCACTTGAACCCGGAAGGTGGAGGTTGCAGTGAGCCAAGATCGCTCC GAGGCTGAGGCAGGAGAATCACTTGAACCCGGCAGGTGGAGGTTGCAGTGAGCCAAGATCGCTCC A C EIF3K Ensembl:ENSG00000178982 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs915634410 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115504,RMVar_hsa_circ_87615,RMVar_hsa_circ_194620,RMVar_hsa_circ_81561,RMVar_hsa_circ_194621,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 26560 RMVar_ID_26560 Human_SNP_ID_665315086 A-to-I Human chr19 + 38650872 38650872 38650872 ATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGAATACGGGCATGCGCCACCACGCCTGGCTTTTT ATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGGATACGGGCATGCGCCACCACGCCTGGCTTTTT A G ACTN4 Ensembl:ENSG00000130402 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1244475169 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_194638,RMVar_hsa_circ_113008,RMVar_hsa_circ_77110,RMVar_hsa_circ_194637 26561 RMVar_ID_26561 Human_SNP_ID_665318123 A-to-I Human chr19 + 38663094 38663094 38663094 ACCACGCCTAGCTAGTTTTTTGTATTTTTAGTAGAGACGGGGTTTCATCATGTTGGCCGGGCTGG ACCACGCCTAGCTAGTTTTTTGTATTTTTAGTGGAGACGGGGTTTCATCATGTTGGCCGGGCTGG A G ACTN4 Ensembl:ENSG00000130402 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1313970995 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_194638,RMVar_hsa_circ_113008,RMVar_hsa_circ_77110,RMVar_hsa_circ_194637 26562 RMVar_ID_26562 Human_SNP_ID_665363539 A-to-I Human chr19 - 38816471 38816471 38816471 TGCCGATGTAGGAACACTGCAGCGCCTGCCCAAGGTCATCGGGAACCAGAGGTGGGTGCAGGGGG TGCCGATGTAGGAACACTGCAGCGCCTGCCCAGGGTCATCGGGAACCAGAGGTGGGTGCAGGGGG T C ECH1 Ensembl:ENSG00000104823 Protein coding CDS GSE100210;GSE112787 HepG2 cell line;293 Flip-In T-REx cells,empty vector - 29129909,29967493 RNA-Seq:(High) rs902757090 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_521207,Human_RBP_ID_825570,Human_RBP_ID_913569,Human_RBP_ID_8833587,Human_RBP_ID_22070171,Human_RBP_ID_22446715 Human_Splice_Rec_2003850,Human_Splice_Rec_2003851,Human_Splice_Rec_2003860,Human_Splice_Rec_2003861,Human_Splice_Rec_2003876,Human_Splice_Rec_2003877,Human_Splice_Rec_2003890,Human_Splice_Rec_2003891,Human_Splice_Rec_2003904 RMVar_hsa_circ_75882,RMVar_hsa_circ_116023,RMVar_hsa_circ_84905,RMVar_hsa_circ_194668,RMVar_hsa_circ_81979,RMVar_hsa_circ_194666,RMVar_hsa_circ_194667,RMVar_hsa_circ_194673 26563 RMVar_ID_26563 Human_SNP_ID_665366939 A-to-I Human chr19 - 38828324 38828324 38828324 GAGAGCCTGAGGCAGGAGAATCGCTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCCTACATCACG GAGAGCCTGAGGCAGGAGAATCGCTTGAACCCGGGAGGCAGAGGTTGCAGTGAGCCTACATCACG T C AC008982.1,ECH1 Ensembl:ENSG00000268083,Ensembl:ENSG00000104823 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1300987376 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75882,RMVar_hsa_circ_194673 26564 RMVar_ID_26564 Human_SNP_ID_665366961 A-to-I Human chr19 - 38828399 38828399 38828399 GGTGAAACCCCGTCTGTACTAAAAATACAAAAATTTTCCCGGCGTGGTGGTGCATGCCTGTAATC GGTGAAACCCCGTCTGTACTAAAAATACAAAATTTTTCCCGGCGTGGTGGTGCATGCCTGTAATC T A AC008982.1,ECH1 Ensembl:ENSG00000268083,Ensembl:ENSG00000104823 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs545687941 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75882,RMVar_hsa_circ_194673 26565 RMVar_ID_26565 Human_SNP_ID_665366973 A-to-I Human chr19 - 38828433 38828433 38828433 GAGGTCAGGAGTTCAAGACTAGCCTGGCCAACATGGTGAAACCCCGTCTGTACTAAAAATACAAA GAGGTCAGGAGTTCAAGACTAGCCTGGCCAACGTGGTGAAACCCCGTCTGTACTAAAAATACAAA T C AC008982.1,ECH1 Ensembl:ENSG00000268083,Ensembl:ENSG00000104823 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs772940818 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75882,RMVar_hsa_circ_194673 26566 RMVar_ID_26566 Human_SNP_ID_665367286 A-to-I Human chr19 - 38829575 38829575 38829575 CTGACCTCGTGATCTGCCCGCCTCGGCCTCCAAAAGTGCTGAGATTACAGGCGTGAGCTACCACG CTGACCTCGTGATCTGCCCGCCTCGGCCTCCATAAGTGCTGAGATTACAGGCGTGAGCTACCACG T A AC008982.1,ECH1 Ensembl:ENSG00000268083,Ensembl:ENSG00000104823 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417891092 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75882,RMVar_hsa_circ_194673 26567 RMVar_ID_26567 Human_SNP_ID_665367287 A-to-I Human chr19 - 38829575 38829575 38829575 CTGACCTCGTGATCTGCCCGCCTCGGCCTCCAAAAGTGCTGAGATTACAGGCGTGAGCTACCACG CTGACCTCGTGATCTGCCCGCCTCGGCCTCCAGAAGTGCTGAGATTACAGGCGTGAGCTACCACG T C AC008982.1,ECH1 Ensembl:ENSG00000268083,Ensembl:ENSG00000104823 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417891092 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75882,RMVar_hsa_circ_194673 26568 RMVar_ID_26568 Human_SNP_ID_665367374 A-to-I Human chr19 - 38829904 38829904 38829904 TCATCCACCCACCTAGGGCCTCCCAAAGTGCTAGGATGATAGGCGTGAGCCACCGTGCCCAGCTA TCATCCACCCACCTAGGGCCTCCCAAAGTGCTGGGATGATAGGCGTGAGCCACCGTGCCCAGCTA T C AC008982.1,ECH1 Ensembl:ENSG00000268083,Ensembl:ENSG00000104823 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1159382524 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75882,RMVar_hsa_circ_194673 26569 RMVar_ID_26569 Human_SNP_ID_665369806 A-to-I Human chr19 - 38837293 38837272 38837293 CAGGCCAGGGATGTCCTTCCTGCCCTTGAGATAGGACCCCGGGATCTTCGCACTGTTGGTGACAC CAGGCCAGGGATGTCCTTCCTGCCCTTGAGAT_____________________TGTTGGTGACAC AGTGCGAAGATCCCGGGGTCCT A AC008982.1,HNRNPL Ensembl:ENSG00000268083,Ensembl:ENSG00000104824 Protein coding,Protein coding intron,intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1422730044 Functional Loss DEL dbSNP153 33..53 33 - - - Human_RBP_ID_1564202,Human_RBP_ID_1887102,Human_RBP_ID_13450537,Human_RBP_ID_19090083,Human_RBP_ID_22359365,Human_RBP_ID_22476617,Human_RBP_ID_22810667,Human_RBP_ID_23257527 RMVar_hsa_circ_83470,RMVar_hsa_circ_119371,RMVar_hsa_circ_194674,RMVar_hsa_circ_194675 26570 RMVar_ID_26570 Human_SNP_ID_665372495 A-to-I Human chr19 - 38844997 38844997 38844997 ATTTATTTAAAAGGGGATATGGGGCCGGGCACAGTGGCTCATGCCTGCAATCCCAGCACTTTCGG ATTTATTTAAAAGGGGATATGGGGCCGGGCACGGTGGCTCATGCCTGCAATCCCAGCACTTTCGG T C HNRNPL,AC008982.2 Ensembl:ENSG00000104824,Ensembl:ENSG00000269688 Protein coding,lincRNA intron,intron GSE38233;GSE99789 cultured B-cells;esophageal squamous carcinoma cells,EC109 - 24183664,29796672 RNA-Seq:(High) rs1457486300 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1575463,Human_RBP_ID_4560524,Human_RBP_ID_5193910,Human_RBP_ID_6760167,Human_RBP_ID_17568051,Human_RBP_ID_23177655 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 26571 RMVar_ID_26571 Human_SNP_ID_665372496 A-to-I Human chr19 - 38844997 38844997 38844997 ATTTATTTAAAAGGGGATATGGGGCCGGGCACAGTGGCTCATGCCTGCAATCCCAGCACTTTCGG ATTTATTTAAAAGGGGATATGGGGCCGGGCACCGTGGCTCATGCCTGCAATCCCAGCACTTTCGG T G HNRNPL,AC008982.2 Ensembl:ENSG00000104824,Ensembl:ENSG00000269688 Protein coding,lincRNA intron,intron GSE38233;GSE99789 cultured B-cells;esophageal squamous carcinoma cells,EC109 - 24183664,29796672 RNA-Seq:(High) rs1457486300 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1575463,Human_RBP_ID_4560524,Human_RBP_ID_5193910,Human_RBP_ID_6760167,Human_RBP_ID_17568051,Human_RBP_ID_23177655 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 26572 RMVar_ID_26572 Human_SNP_ID_665372550 A-to-I Human chr19 - 38845162 38845162 38845162 CAGGCAATCCACTTGCCTCAGCCTCCCAGATTACAGGTGTGAGCCACCGCGCCTGGCTAGGAATT CAGGCAATCCACTTGCCTCAGCCTCCCAGATTCCAGGTGTGAGCCACCGCGCCTGGCTAGGAATT T G HNRNPL,AC008982.2 Ensembl:ENSG00000104824,Ensembl:ENSG00000269688 Protein coding,lincRNA intron,intron GSE38233;GSE100210;GSE99789 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 24183664,29129909,29796672 RNA-Seq:(High) rs994639617 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5249054 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 26573 RMVar_ID_26573 Human_SNP_ID_665372604 A-to-I Human chr19 - 38845289 38845289 38845289 TCAGCTCACTGCAACCTCTGCCTCCTGGGTTCAAGCAATTCTCCTGCCTCAGCCTTCCTAGTAGG TCAGCTCACTGCAACCTCTGCCTCCTGGGTTCGAGCAATTCTCCTGCCTCAGCCTTCCTAGTAGG T C HNRNPL,AC008982.2 Ensembl:ENSG00000104824,Ensembl:ENSG00000269688 Protein coding,lincRNA intron,exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1174548876 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2004149 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 26574 RMVar_ID_26574 Human_SNP_ID_665380469 A-to-I Human chr19 - 38868411 38868411 38868411 CCAGGCTGGTCTCAAACTCCTAACCTCAAGCAATCTGCCCACGTCGGCCTCCCAAAGTGCTGAGA CCAGGCTGGTCTCAAACTCCTAACCTCAAGCAGTCTGCCCACGTCGGCCTCCCAAAGTGCTGAGA T C RINL Ensembl:ENSG00000187994 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1301534070 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26472469 26575 RMVar_ID_26575 Human_SNP_ID_665381958 A-to-I Human chr19 - 38873053 38873049 38873053 TTCTTTTTCTTTTTTCTTTTAGACAGAGTCTCACTCTGTCGCTCAGGCGGAGTGCAGTGGCCCAA TTCTTTTTCTTTTTTCTTTTAGACAGAGTCTC____TGTCGCTCAGGCGGAGTGCAGTGGCCCAA AGAGT A RINL Ensembl:ENSG00000187994 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs894060030 Functional Loss DEL dbSNP153 33..36 33 - - - 26576 RMVar_ID_26576 Human_SNP_ID_665382795 A-to-I Human chr19 - 38876162 38876162 38876162 CTAGCTACTCATGAGGCTGAGGTGGGAGGATCATTTGAGCTCAGGAGGTCAAGGCGGCAGTGAGC CTAGCTACTCATGAGGCTGAGGTGGGAGGATCTTTTGAGCTCAGGAGGTCAAGGCGGCAGTGAGC T A RINL Ensembl:ENSG00000187994 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs987870916 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_194687,RMVar_hsa_circ_102904 26577 RMVar_ID_26577 Human_SNP_ID_665386372 A-to-I Human chr19 - 38889108 38889108 38889108 TACTTCATGCGCCTGCTGAAGGACAAGGGGCTACTCCTGCGCTGCTACACGCAGGTAGGCGGATG TACTTCATGCGCCTGCTGAAGGACAAGGGGCTGCTCCTGCGCTGCTACACGCAGGTAGGCGGATG T C SIRT2 Ensembl:ENSG00000068903 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1226048396 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_914718,Human_RBP_ID_3954982,Human_RBP_ID_26337863,Human_RBP_ID_26815839 Human_Splice_Rec_2004250,Human_Splice_Rec_2004251,Human_Splice_Rec_2004265,Human_Splice_Rec_2004278,Human_Splice_Rec_2004279,Human_Splice_Rec_2004306,Human_Splice_Rec_2004307,Human_Splice_Rec_2004336,Human_Splice_Rec_2004337,Human_Splice_Rec_2004364,Human_Splice_Rec_2004365,Human_Splice_Rec_2004400,Human_Splice_Rec_2004401,Human_Splice_Rec_2004422,Human_Splice_Rec_2004423,Human_Splice_Rec_2004442,Human_Splice_Rec_2004443,Human_Splice_Rec_2004460,Human_Splice_Rec_2004461,Human_Splice_Rec_2004472 RMVar_hsa_circ_51586,RMVar_hsa_circ_334297,RMVar_hsa_circ_194694 26578 RMVar_ID_26578 Human_SNP_ID_665387425 A-to-I Human chr19 - 38892666 38892666 38892666 AGGAGGCTGAGAAGGGAGGATTGTTTGAGCCCAGGAATTGGAGGCTGCAGTGAGCTATGATGGCA AGGAGGCTGAGAAGGGAGGATTGTTTGAGCCCGGGAATTGGAGGCTGCAGTGAGCTATGATGGCA T C SIRT2 Ensembl:ENSG00000068903 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs970400517 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51586 26579 RMVar_ID_26579 Human_SNP_ID_665387426 A-to-I Human chr19 - 38892666 38892666 38892666 AGGAGGCTGAGAAGGGAGGATTGTTTGAGCCCAGGAATTGGAGGCTGCAGTGAGCTATGATGGCA AGGAGGCTGAGAAGGGAGGATTGTTTGAGCCCCGGAATTGGAGGCTGCAGTGAGCTATGATGGCA T G SIRT2 Ensembl:ENSG00000068903 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs970400517 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51586 26580 RMVar_ID_26580 Human_SNP_ID_665388269 A-to-I Human chr19 - 38895765 38895765 38895765 CTCAGCCTTTCTCTCTCTTTTTAAATAGAGACAGAGTCTCACTGTGTTGCCCAGGCTGGTCTTGA CTCAGCCTTTCTCTCTCTTTTTAAATAGAGACGGAGTCTCACTGTGTTGCCCAGGCTGGTCTTGA T C SIRT2 Ensembl:ENSG00000068903 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935197058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25414223 26581 RMVar_ID_26581 Human_SNP_ID_665391798 A-to-I Human chr19 + 38908343 38908343 38908343 CAGGCAGATCACGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGCAAGACCCTGTCTCTAC CAGGCAGATCACGAGGTCAGGAGTTCGAGACCGGCCTGGCCAACATGGCAAGACCCTGTCTCTAC A G NFKBIB Ensembl:ENSG00000104825 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs544582105 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90770,RMVar_hsa_circ_194695 26582 RMVar_ID_26582 Human_SNP_ID_665393567 A-to-I Human chr19 - 38913686 38913686 38913686 TCACTGCAACCTCTGAGAGATTCTTTTGCCTCAGCCTCCCGCATAGCTGGGATTACAGGGAGGTG TCACTGCAACCTCTGAGAGATTCTTTTGCCTCGGCCTCCCGCATAGCTGGGATTACAGGGAGGTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs970014122 Functional Loss SNV dbSNP153 33..33 33 - - - 26583 RMVar_ID_26583 Human_SNP_ID_665397667 A-to-I Human chr19 - 38925213 38925213 38925213 TGCCCCCTGGGTTCAAGTGATTCTTCTGCCTCAGCCTCCCCAGTAGCTGGGATTACAGACATGCG TGCCCCCTGGGTTCAAGTGATTCTTCTGCCTCGGCCTCCCCAGTAGCTGGGATTACAGACATGCG T C SARS2,AC011455.2 Ensembl:ENSG00000104835,Ensembl:ENSG00000269547 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs566990075 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_349501,RMVar_hsa_circ_194701,RMVar_hsa_circ_106956,RMVar_hsa_circ_194702 26584 RMVar_ID_26584 Human_SNP_ID_665397873 A-to-I Human chr19 - 38926091 38926091 38926091 ACTTGAACAGGCTGGCACGGTGGCTCACGCCTATAATCCCAGCTACTCGGGAGGCCTAGGTTGGT ACTTGAACAGGCTGGCACGGTGGCTCACGCCTGTAATCCCAGCTACTCGGGAGGCCTAGGTTGGT T C SARS2,AC011455.2 Ensembl:ENSG00000104835,Ensembl:ENSG00000269547 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1457987210 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13451276,Human_RBP_ID_25445818 RMVar_hsa_circ_349501,RMVar_hsa_circ_194701,RMVar_hsa_circ_106956,RMVar_hsa_circ_194702 26585 RMVar_ID_26585 Human_SNP_ID_665447731 A-to-I Human chr19 + 39111334 39111334 39111334 ATGGTGGTGTGTGCCTGTAGTCCCAGCTGCTCAGGAGGCTGAGGCGGGAGGATGGCTTGAGCCCA ATGGTGGTGTGTGCCTGTAGTCCCAGCTGCTCGGGAGGCTGAGGCGGGAGGATGGCTTGAGCCCA A G ACP7 Ensembl:ENSG00000183760 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1011950128 Functional Loss SNV dbSNP153 33..33 33 - - - 26586 RMVar_ID_26586 Human_SNP_ID_665525766 A-to-I Human chr19 + 39395019 39395019 39395019 GGGACTACAGGCATGCACTGCCATGCCTGGCTAATTTTTGTATTTTTTGTAGAGACGGGGTTTTG GGGACTACAGGCATGCACTGCCATGCCTGGCTGATTTTTGTATTTTTTGTAGAGACGGGGTTTTG A G MED29 Ensembl:ENSG00000063322 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037822373 Functional Loss SNV dbSNP153 33..33 33 - - - 26587 RMVar_ID_26587 Human_SNP_ID_665535968 A-to-I Human chr19 + 39427564 39427563 39427565 CCAGGCCATAGTGGTCTTGGACTCCTGACCTCAGGTGATCCGCCCACCTCGGCCTCCCAAAGTGT CCAGGCCATAGTGGTCTTGGACTCCTGACCTC__GTGATCCGCCCACCTCGGCCTCCCAAAGTGT CAG C PLEKHG2 Ensembl:ENSG00000090924 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1312776150 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_88824,RMVar_hsa_circ_194740 26588 RMVar_ID_26588 Human_SNP_ID_665535972 A-to-I Human chr19 + 39427577 39427577 39427577 GTCTTGGACTCCTGACCTCAGGTGATCCGCCCACCTCGGCCTCCCAAAGTGTTGGGTTTACAGGC GTCTTGGACTCCTGACCTCAGGTGATCCGCCCGCCTCGGCCTCCCAAAGTGTTGGGTTTACAGGC A G PLEKHG2 Ensembl:ENSG00000090924 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1239424704 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88824,RMVar_hsa_circ_194740 26589 RMVar_ID_26589 Human_SNP_ID_665536063 A-to-I Human chr19 + 39427974 39427974 39427974 CCTGTAATCCCAACACTTCGTGAGGCCAAGGCAGGTGGATCACTTGAAGTGAGGAGTTCGAGACC CCTGTAATCCCAACACTTCGTGAGGCCAAGGCGGGTGGATCACTTGAAGTGAGGAGTTCGAGACC A G PLEKHG2 Ensembl:ENSG00000090924 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1256154241 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88824,RMVar_hsa_circ_194740 26590 RMVar_ID_26590 Human_SNP_ID_665536086 A-to-I Human chr19 + 39428052 39428052 39428052 CAACATGGTGAAATCCCGTCTTTACTAAAAATACAAAAAATTAGCTGGGCGTGGTGGTGGGTGCC CAACATGGTGAAATCCCGTCTTTACTAAAAATTCAAAAAATTAGCTGGGCGTGGTGGTGGGTGCC A T PLEKHG2 Ensembl:ENSG00000090924 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs545224016 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88824,RMVar_hsa_circ_194740 26591 RMVar_ID_26591 Human_SNP_ID_665536087 A-to-I Human chr19 + 39428054 39428053 39428054 ACATGGTGAAATCCCGTCTTTACTAAAAATACAAAAAATTAGCTGGGCGTGGTGGTGGGTGCCGG ACATGGTGAAATCCCGTCTTTACTAAAAATAC_AAAAATTAGCTGGGCGTGGTGGTGGGTGCCGG CA C PLEKHG2 Ensembl:ENSG00000090924 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1236861639 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_88824,RMVar_hsa_circ_194740 26592 RMVar_ID_26592 Human_SNP_ID_665536088 A-to-I Human chr19 + 39428054 39428054 39428054 ACATGGTGAAATCCCGTCTTTACTAAAAATACAAAAAATTAGCTGGGCGTGGTGGTGGGTGCCGG ACATGGTGAAATCCCGTCTTTACTAAAAATACCAAAAATTAGCTGGGCGTGGTGGTGGGTGCCGG A C PLEKHG2 Ensembl:ENSG00000090924 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1462412787 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88824,RMVar_hsa_circ_194740 26593 RMVar_ID_26593 Human_SNP_ID_665536105 A-to-I Human chr19 + 39428102 39428102 39428102 GTGGTGGTGGGTGCCGGTAATCCTAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCTG GTGGTGGTGGGTGCCGGTAATCCTAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCTG A G PLEKHG2 Ensembl:ENSG00000090924 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs993989607 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88824,RMVar_hsa_circ_194740 26594 RMVar_ID_26594 Human_SNP_ID_665536106 A-to-I Human chr19 + 39428102 39428102 39428102 GTGGTGGTGGGTGCCGGTAATCCTAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCTG GTGGTGGTGGGTGCCGGTAATCCTAGCTACTCTGGAGGCTGAGGCAGGAGAATCACTTGAACCTG A T PLEKHG2 Ensembl:ENSG00000090924 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs993989607 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88824,RMVar_hsa_circ_194740 26595 RMVar_ID_26595 Human_SNP_ID_665536125 A-to-I Human chr19 + 39428172 39428172 39428172 TGGAGGTTGCAGTGAACCGAGATTGCGCCACTAGACTCCAGCCTGGGAGACGAGCAAAACTGTCT TGGAGGTTGCAGTGAACCGAGATTGCGCCACTGGACTCCAGCCTGGGAGACGAGCAAAACTGTCT A G PLEKHG2 Ensembl:ENSG00000090924 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs531250798 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25415848 RMVar_hsa_circ_88824,RMVar_hsa_circ_194740 26596 RMVar_ID_26596 Human_SNP_ID_665544273 A-to-I Human chr19 + 39454375 39454371 39454375 TGTTGTTGTCGTTGTTTTTTTTTTTTTTTTTGAGACGGAGTCTCGCTCAGGCTGGAGTGCAGTGG TGTTGTTGTCGTTGTTTTTTTTTTTTTTT____GACGGAGTCTCGCTCAGGCTGGAGTGCAGTGG TTTGA T SUPT5H Ensembl:ENSG00000196235 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1490871049 Functional Loss DEL dbSNP153 30..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 26597 RMVar_ID_26597 Human_SNP_ID_665544276 A-to-I Human chr19 + 39454375 39454372 39454375 TGTTGTTGTCGTTGTTTTTTTTTTTTTTTTTGAGACGGAGTCTCGCTCAGGCTGGAGTGCAGTGG TGTTGTTGTCGTTGTTTTTTTTTTTTTTTT___GACGGAGTCTCGCTCAGGCTGGAGTGCAGTGG TTGA T SUPT5H Ensembl:ENSG00000196235 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1197343509 Functional Loss DEL dbSNP153 31..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 26598 RMVar_ID_26598 Human_SNP_ID_665546569 A-to-I Human chr19 + 39462084 39462084 39462084 CATCCGCCACCATGCCCGGCTGATTTTTTTGTATTTTTAATAGAGACGGGGTTTCACCATGTTGG CATCCGCCACCATGCCCGGCTGATTTTTTTGTGTTTTTAATAGAGACGGGGTTTCACCATGTTGG A G SUPT5H Ensembl:ENSG00000196235 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1180901486 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21687,RMVar_hsa_circ_194759,RMVar_hsa_circ_85628,RMVar_hsa_circ_106071,RMVar_hsa_circ_377662,RMVar_hsa_circ_194761,RMVar_hsa_circ_115416,RMVar_hsa_circ_194763 26599 RMVar_ID_26599 Human_SNP_ID_665554891 A-to-I Human chr19 + 39490395 39490395 39490395 AAGAACTTGGGAATATTTTTTTTTTTTTTTTGAGACAGGGTCTCACTGTTGCCCAGGCTGGAGTG AAGAACTTGGGAATATTTTTTTTTTTTTTTTGGGACAGGGTCTCACTGTTGCCCAGGCTGGAGTG A G TIMM50 Ensembl:ENSG00000105197 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs537437016 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5650148,Human_RBP_ID_6762005,Human_RBP_ID_17569026,Human_RBP_ID_22370915,Human_RBP_ID_23178076,Human_RBP_ID_26468230 RMVar_hsa_circ_104877,RMVar_hsa_circ_194777 26600 RMVar_ID_26600 Human_SNP_ID_665554907 A-to-I Human chr19 + 39490450 39490450 39490450 GGCTGGAGTGCATTGATGTGATCTTAGCTTACAACAGCCTTGACCTCCCGGCTCAAGTGATCTCC GGCTGGAGTGCATTGATGTGATCTTAGCTTACGACAGCCTTGACCTCCCGGCTCAAGTGATCTCC A G TIMM50 Ensembl:ENSG00000105197 Protein coding 3'UTR GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,29796672,31158229,31158229,32596459 RNA-Seq:(High) rs958598716 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4528038,Human_RBP_ID_5650148,Human_RBP_ID_17569026,Human_RBP_ID_22371158,Human_RBP_ID_23178078,Human_RBP_ID_26468232 RMVar_hsa_circ_104877,RMVar_hsa_circ_194777 26601 RMVar_ID_26601 Human_SNP_ID_665554953 A-to-I Human chr19 + 39490624 39490624 39490624 GGTGCCCAAGCTGGTCTCAAACTCCTAGTCTTAAGCAATCTTCCTGCTTTGGCCTCCCAAAGCGC GGTGCCCAAGCTGGTCTCAAACTCCTAGTCTTGAGCAATCTTCCTGCTTTGGCCTCCCAAAGCGC A G TIMM50 Ensembl:ENSG00000105197 Protein coding 3'UTR GSE47997;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 23474544,31158229,31158229 RNA-Seq:(High) rs1168582721 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4528043,Human_RBP_ID_22371159,Human_RBP_ID_26468238 RMVar_hsa_circ_104877,RMVar_hsa_circ_194777 26602 RMVar_ID_26602 Human_SNP_ID_665554961 A-to-I Human chr19 + 39490658 39490658 39490658 GCAATCTTCCTGCTTTGGCCTCCCAAAGCGCTAGGATTCCAGGTGTGAGCTACTGTGCCCAGCTA GCAATCTTCCTGCTTTGGCCTCCCAAAGCGCTGGGATTCCAGGTGTGAGCTACTGTGCCCAGCTA A G TIMM50 Ensembl:ENSG00000105197 Protein coding 3'UTR GSE47997;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs562415814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26468239 RMVar_hsa_circ_104877,RMVar_hsa_circ_194777 26603 RMVar_ID_26603 Human_SNP_ID_665554973 A-to-I Human chr19 + 39490720 39490720 39490720 CTAAAATAGGGATTTTTATATTAAATCTCCCTATTTTAAAATGTTGGCTCCTAGCGGGGCGCAGT CTAAAATAGGGATTTTTATATTAAATCTCCCTGTTTTAAAATGTTGGCTCCTAGCGGGGCGCAGT A G TIMM50 Ensembl:ENSG00000105197 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1047703330 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17924663,Human_RBP_ID_23178085,Human_RBP_ID_26468241 RMVar_hsa_circ_104877,RMVar_hsa_circ_194777 26604 RMVar_ID_26604 Human_SNP_ID_665555216 A-to-I Human chr19 + 39491537 39491537 39491537 TGACTGAGAAACTGAATTTTTAATTTTGTTTGAGACTGGGCACAGTGGCTCACGCCTGTAATCCT TGACTGAGAAACTGAATTTTTAATTTTGTTTGCGACTGGGCACAGTGGCTCACGCCTGTAATCCT A C TIMM50 Ensembl:ENSG00000105197 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1384999144 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_521799,Human_RBP_ID_1887592,Human_RBP_ID_6762019,Human_RBP_ID_13454129,Human_RBP_ID_17567680,Human_RBP_ID_17924666,Human_RBP_ID_18305116,Human_RBP_ID_22371160,Human_RBP_ID_22972648,Human_RBP_ID_23178096,Human_RBP_ID_26468247 26605 RMVar_ID_26605 Human_SNP_ID_665555258 A-to-I Human chr19 + 39491689 39491689 39491689 AAAAAAAACAAAGTAACGAGCCCAGCGAGGTTATGCATACCTGTAGTCCCAGCTACGTGAGAGGC AAAAAAAACAAAGTAACGAGCCCAGCGAGGTTGTGCATACCTGTAGTCCCAGCTACGTGAGAGGC A G TIMM50 Ensembl:ENSG00000105197 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs112700531 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4528058,Human_RBP_ID_22371161,Human_RBP_ID_26468251 26606 RMVar_ID_26606 Human_SNP_ID_665555280 A-to-I Human chr19 + 39491769 39491766 39491769 CCCTTGAGCCAAGGAGGTCGTGCGTGGCTGTGATGATCTGTGATCGTGCCGCTAAATTCTAGCCT CCCTTGAGCCAAGGAGGTCGTGCGTGGCTG___TGATCTGTGATCGTGCCGCTAAATTCTAGCCT GTGA G TIMM50 Ensembl:ENSG00000105197 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1433940017 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_279643,Human_RBP_ID_8487359,Human_RBP_ID_13454136,Human_RBP_ID_26468252 26607 RMVar_ID_26607 Human_SNP_ID_665555281 A-to-I Human chr19 + 39491769 39491769 39491769 CCCTTGAGCCAAGGAGGTCGTGCGTGGCTGTGATGATCTGTGATCGTGCCGCTAAATTCTAGCCT CCCTTGAGCCAAGGAGGTCGTGCGTGGCTGTGGTGATCTGTGATCGTGCCGCTAAATTCTAGCCT A G TIMM50 Ensembl:ENSG00000105197 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1003404486 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_279643,Human_RBP_ID_8487359,Human_RBP_ID_13454136,Human_RBP_ID_26468252 26608 RMVar_ID_26608 Human_SNP_ID_665555291 A-to-I Human chr19 + 39491790 39491790 39491790 GCGTGGCTGTGATGATCTGTGATCGTGCCGCTAAATTCTAGCCTGGGCAACAGAGCGAGACCCTG GCGTGGCTGTGATGATCTGTGATCGTGCCGCTGAATTCTAGCCTGGGCAACAGAGCGAGACCCTG A G TIMM50 Ensembl:ENSG00000105197 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1288863521 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9921719,Human_RBP_ID_22979320,Human_RBP_ID_25446144,Human_RBP_ID_26468252 26609 RMVar_ID_26609 Human_SNP_ID_665555359 A-to-I Human chr19 + 39491871 39491871 39491871 AAAAAAAAAAAAACCTTAAGATTTTTTTTTGGAGTCAGGGTCTCGCTGTGTCGCCCAGGCTGGAG AAAAAAAAAAAAACCTTAAGATTTTTTTTTGGGGTCAGGGTCTCGCTGTGTCGCCCAGGCTGGAG A G TIMM50 Ensembl:ENSG00000105197 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049306872 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23178104,Human_RBP_ID_26474971 26610 RMVar_ID_26610 Human_SNP_ID_665555386 A-to-I Human chr19 + 39491979 39491979 39491979 GCTCAAACAATCTTCCTGCCTTGGCCTCCCCAAATGCTGAGATTATAGGAGTGAGCCACTCTGCC GCTCAAACAATCTTCCTGCCTTGGCCTCCCCACATGCTGAGATTATAGGAGTGAGCCACTCTGCC A C TIMM50 Ensembl:ENSG00000105197 Protein coding 3'UTR GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,29796672,31158229,31158229 RNA-Seq:(High) rs1403987140 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6804553,Human_RBP_ID_13454141,Human_RBP_ID_18732570,Human_RBP_ID_26473996,Human_RBP_ID_27468098 26611 RMVar_ID_26611 Human_SNP_ID_665555389 A-to-I Human chr19 + 39491991 39491991 39491991 TTCCTGCCTTGGCCTCCCCAAATGCTGAGATTATAGGAGTGAGCCACTCTGCCCAACTACTTTTA TTCCTGCCTTGGCCTCCCCAAATGCTGAGATTGTAGGAGTGAGCCACTCTGCCCAACTACTTTTA A G TIMM50 Ensembl:ENSG00000105197 Protein coding 3'UTR GSE38233;GSE100210;GSE99789 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 24183664,29129909,29796672 RNA-Seq:(High) rs1333385133 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6804553,Human_RBP_ID_13454141,Human_RBP_ID_17695705,Human_RBP_ID_18514929,Human_RBP_ID_18732570,Human_RBP_ID_26468257,Human_RBP_ID_27468098 26612 RMVar_ID_26612 Human_SNP_ID_665555629 A-to-I Human chr19 + 39492724 39492724 39492724 CCCTGTCTCTACTAAAAAAATACAAATAAATTAGCTGGGCATGGTGGTGGGTGCCTGTAATCCCA CCCTGTCTCTACTAAAAAAATACAAATAAATTGGCTGGGCATGGTGGTGGGTGCCTGTAATCCCA A G TIMM50 Ensembl:ENSG00000105197 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs889469673 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17924675 26613 RMVar_ID_26613 Human_SNP_ID_665555673 A-to-I Human chr19 + 39492853 39492852 39492854 AGATCACACCATTGCACTCCAGCCTGGGCGACAGAGTAAGGCTCTGTCTCCAAAAAAAAAAAAAA AGATCACACCATTGCACTCCAGCCTGGGCGAC__AGTAAGGCTCTGTCTCCAAAAAAAAAAAAAA CAG C TIMM50 Ensembl:ENSG00000105197 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1283711284 Functional Loss DEL dbSNP153 33..34 33 - - - 26614 RMVar_ID_26614 Human_SNP_ID_665555675 A-to-I Human chr19 + 39492858 39492858 39492858 ACACCATTGCACTCCAGCCTGGGCGACAGAGTAAGGCTCTGTCTCCAAAAAAAAAAAAAAAAAAA ACACCATTGCACTCCAGCCTGGGCGACAGAGTGAGGCTCTGTCTCCAAAAAAAAAAAAAAAAAAA A G TIMM50 Ensembl:ENSG00000105197 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1312797600 Functional Loss SNV dbSNP153 33..33 33 - - - 26615 RMVar_ID_26615 Human_SNP_ID_665555804 A-to-I Human chr19 + 39492894 39492893 39492894 CTCTGTCTCCAAAAAAAAAAAAAAAAAAAAACAAAAAAAAAACCAGTTTGACTTTATCTCCCTCG CTCTGTCTCCAAAAAAAAAAAAAAAAAAAAAC_AAAAAAAAACCAGTTTGACTTTATCTCCCTCG CA C TIMM50 Ensembl:ENSG00000105197 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1159452213 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_521807,Human_RBP_ID_23178122 26616 RMVar_ID_26616 Human_SNP_ID_665555807 A-to-I Human chr19 + 39492894 39492894 39492894 CTCTGTCTCCAAAAAAAAAAAAAAAAAAAAACAAAAAAAAAACCAGTTTGACTTTATCTCCCTCG CTCTGTCTCCAAAAAAAAAAAAAAAAAAAAACCAAAAAAAAACCAGTTTGACTTTATCTCCCTCG A C TIMM50 Ensembl:ENSG00000105197 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1408489384 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_521807,Human_RBP_ID_23178122 26617 RMVar_ID_26617 Human_SNP_ID_665555808 A-to-I Human chr19 + 39492895 39492895 39492895 TCTGTCTCCAAAAAAAAAAAAAAAAAAAAACAAAAAAAAAACCAGTTTGACTTTATCTCCCTCGC TCTGTCTCCAAAAAAAAAAAAAAAAAAAAACACAAAAAAAACCAGTTTGACTTTATCTCCCTCGC A C TIMM50 Ensembl:ENSG00000105197 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1365251890 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_521807,Human_RBP_ID_23178122 26618 RMVar_ID_26618 Human_SNP_ID_665555809 A-to-I Human chr19 + 39492896 39492896 39492896 CTGTCTCCAAAAAAAAAAAAAAAAAAAAACAAAAAAAAAACCAGTTTGACTTTATCTCCCTCGCC CTGTCTCCAAAAAAAAAAAAAAAAAAAAACAAGAAAAAAACCAGTTTGACTTTATCTCCCTCGCC A G TIMM50 Ensembl:ENSG00000105197 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1191348066 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_521807,Human_RBP_ID_23178122 26619 RMVar_ID_26619 Human_SNP_ID_665555810 A-to-I Human chr19 + 39492897 39492897 39492897 TGTCTCCAAAAAAAAAAAAAAAAAAAAACAAAAAAAAAACCAGTTTGACTTTATCTCCCTCGCCC TGTCTCCAAAAAAAAAAAAAAAAAAAAACAAACAAAAAACCAGTTTGACTTTATCTCCCTCGCCC A C TIMM50 Ensembl:ENSG00000105197 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1157586691 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_521807,Human_RBP_ID_23178122 26620 RMVar_ID_26620 Human_SNP_ID_665555811 A-to-I Human chr19 + 39492897 39492897 39492897 TGTCTCCAAAAAAAAAAAAAAAAAAAAACAAAAAAAAAACCAGTTTGACTTTATCTCCCTCGCCC TGTCTCCAAAAAAAAAAAAAAAAAAAAACAAAGAAAAAACCAGTTTGACTTTATCTCCCTCGCCC A G TIMM50 Ensembl:ENSG00000105197 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1157586691 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_521807,Human_RBP_ID_23178122 26621 RMVar_ID_26621 Human_SNP_ID_665555812 A-to-I Human chr19 + 39492898 39492898 39492898 GTCTCCAAAAAAAAAAAAAAAAAAAAACAAAAAAAAAACCAGTTTGACTTTATCTCCCTCGCCCT GTCTCCAAAAAAAAAAAAAAAAAAAAACAAAACAAAAACCAGTTTGACTTTATCTCCCTCGCCCT A C TIMM50 Ensembl:ENSG00000105197 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941290315 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_521807,Human_RBP_ID_23178122 26622 RMVar_ID_26622 Human_SNP_ID_665555949 A-to-I Human chr19 + 39493324 39493324 39493324 CAGGCTGGAGTGCAGTGGGGCGATCTCGGCTCACTGCACCCTGCACCTCCTGGGTTCAAGTGATT CAGGCTGGAGTGCAGTGGGGCGATCTCGGCTCCCTGCACCCTGCACCTCCTGGGTTCAAGTGATT A C TIMM50 Ensembl:ENSG00000105197 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1189780843 Functional Loss SNV dbSNP153 33..33 33 - - - 26623 RMVar_ID_26623 Human_SNP_ID_665555950 A-to-I Human chr19 + 39493324 39493324 39493324 CAGGCTGGAGTGCAGTGGGGCGATCTCGGCTCACTGCACCCTGCACCTCCTGGGTTCAAGTGATT CAGGCTGGAGTGCAGTGGGGCGATCTCGGCTCGCTGCACCCTGCACCTCCTGGGTTCAAGTGATT A G TIMM50 Ensembl:ENSG00000105197 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1189780843 Functional Loss SNV dbSNP153 33..33 33 - - - 26624 RMVar_ID_26624 Human_SNP_ID_665555957 A-to-I Human chr19 + 39493349 39493349 39493349 TCGGCTCACTGCACCCTGCACCTCCTGGGTTCAAGTGATTCTCCTGCCTCAGGCTCCCAAGTAGC TCGGCTCACTGCACCCTGCACCTCCTGGGTTCTAGTGATTCTCCTGCCTCAGGCTCCCAAGTAGC A T TIMM50 Ensembl:ENSG00000105197 Protein coding 3'UTR GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 29129909,30559470 RNA-Seq:(High) rs935014488 Functional Loss SNV dbSNP153 33..33 33 - - - 26625 RMVar_ID_26625 Human_SNP_ID_665668475 A-to-I Human chr19 - 39910175 39910175 39910175 TGTAGATATGATATTTATTTATTTTTGAGATAAGGTATTATCCTGTCACCGAGGCTGGAGTCCAG TGTAGATATGATATTTATTTATTTTTGAGATAGGGTATTATCCTGTCACCGAGGCTGGAGTCCAG T C FCGBP Ensembl:ENSG00000275395 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934622838 Functional Loss SNV dbSNP153 33..33 33 - - - 26626 RMVar_ID_26626 Human_SNP_ID_665691608 A-to-I Human chr19 + 40003311 40003311 40003311 TGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGTGCCCAGCTTAAAATT TGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTGCAGGCGTGAGCCACCGTGCCCAGCTTAAAATT A G ZNF546 Ensembl:ENSG00000187187 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1190651715 Functional Loss SNV dbSNP153 33..33 33 - - - 26627 RMVar_ID_26627 Human_SNP_ID_665691731 A-to-I Human chr19 + 40003937 40003937 40003937 GGGAGCCTGAGGCAGGAGAATCACTTGAACCTAGGAGGCGGAGTCTACAGTGAGCTGAGATTGTG GGGAGCCTGAGGCAGGAGAATCACTTGAACCTGGGAGGCGGAGTCTACAGTGAGCTGAGATTGTG A G ZNF546 Ensembl:ENSG00000187187 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1458582906 Functional Loss SNV dbSNP153 33..33 33 - - - 26628 RMVar_ID_26628 Human_SNP_ID_665696385 A-to-I Human chr19 - 40024300 40024300 40024300 TCAGAGACAGCAACAGAATAGAAATCAGCATCAGAATCTCAGTGGTGCAGGAGATAGAGGAAGTC TCAGAGACAGCAACAGAATAGAAATCAGCATCGGAATCTCAGTGGTGCAGGAGATAGAGGAAGTC T C AC007842.1 Ensembl:ENSG00000269069 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1265667603 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5586260,Human_RBP_ID_18532918 26629 RMVar_ID_26629 Human_SNP_ID_665696492 A-to-I Human chr19 - 40024867 40024867 40024867 CCAGCTTTACCCAACAGAGCCTGTGCAGTCCTATTCCATAGACTTTCCTCCGCCTGAAACCAGCA CCAGCTTTACCCAACAGAGCCTGTGCAGTCCTGTTCCATAGACTTTCCTCCGCCTGAAACCAGCA T C AC007842.1 Ensembl:ENSG00000269069 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs780188067 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5099118,Human_RBP_ID_5586263 26630 RMVar_ID_26630 Human_SNP_ID_665698103 A-to-I Human chr19 - 40032497 40032497 40032497 AGCCAGGATGGTCTCGATCTCCTGACCTCGTGATCCACCCGCCTTGGCCTCCCAAAGTGCTGGGA AGCCAGGATGGTCTCGATCTCCTGACCTCGTGTTCCACCCGCCTTGGCCTCCCAAAGTGCTGGGA T A ZNF780B Ensembl:ENSG00000128000 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1423964720 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114747,RMVar_hsa_circ_194813,RMVar_hsa_circ_194812,RMVar_hsa_circ_194814 26631 RMVar_ID_26631 Human_SNP_ID_665707920 A-to-I Human chr19 - 40075202 40075202 40075202 ACCTTGTTCAACATCAGAGTATTCATGCTGGTATAAAACCATATGAATGTAAGGAGTGTGGGAAA ACCTTGTTCAACATCAGAGTATTCATGCTGGTGTAAAACCATATGAATGTAAGGAGTGTGGGAAA T C ZNF780A,AC005614.2 Ensembl:ENSG00000197782,Ensembl:ENSG00000269749 Protein coding,lincRNA CDS,intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1429728684 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1388631,Human_miRNA_ID_2120876,Human_miRNA_ID_2124092,Human_miRNA_ID_2127313,Human_miRNA_ID_2130531,Human_miRNA_ID_2924096 RMVar_hsa_circ_95105,RMVar_hsa_circ_100241,RMVar_hsa_circ_194819,RMVar_hsa_circ_372750,RMVar_hsa_circ_194820,RMVar_hsa_circ_97248,RMVar_hsa_circ_194823,RMVar_hsa_circ_78041,RMVar_hsa_circ_83137,RMVar_hsa_circ_194824,RMVar_hsa_circ_194825,RMVar_hsa_circ_194821,RMVar_hsa_circ_194822 26632 RMVar_ID_26632 Human_SNP_ID_665738567 A-to-I Human chr19 + 40199713 40199713 40199713 AGCCATGAGGAGCCATGTCTGAATAGAGTGGTAGCTCACACCTATAATCCCAGTACTTTGGGAGG AGCCATGAGGAGCCATGTCTGAATAGAGTGGTGGCTCACACCTATAATCCCAGTACTTTGGGAGG A G MAP3K10 Ensembl:ENSG00000130758 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1392469336 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117982,RMVar_hsa_circ_194829 26633 RMVar_ID_26633 Human_SNP_ID_665739437 A-to-I Human chr19 + 40203294 40203294 40203294 CCAAGAGGCGGAGGTTGCAGGGAGCCGAGATCATGCCACTGCACTCCAGCCTGGGTGACAGAGAC CCAAGAGGCGGAGGTTGCAGGGAGCCGAGATCGTGCCACTGCACTCCAGCCTGGGTGACAGAGAC A G MAP3K10 Ensembl:ENSG00000130758 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs780504158 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117982,RMVar_hsa_circ_194829 26634 RMVar_ID_26634 Human_SNP_ID_665740592 A-to-I Human chr19 + 40207913 40207913 40207913 GTAAATTTTCATTAAAAATTTTTTTTTTTCTGAGATGGGGTCTTGCTATATTGCCCAGGGTGGTC GTAAATTTTCATTAAAAATTTTTTTTTTTCTGGGATGGGGTCTTGCTATATTGCCCAGGGTGGTC A G MAP3K10 Ensembl:ENSG00000130758 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1329553103 Functional Loss SNV dbSNP153 33..33 33 - - - 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 26635 RMVar_ID_26635 Human_SNP_ID_665747959 A-to-I Human chr19 - 40231655 40231655 40231655 GGCGCTGGCCGGATGGAACACCTCCCCCAGCAAGGGACCAGGGACCAGAGCCCTGGCCTGCCCTG GGCGCTGGCCGGATGGAACACCTCCCCCAGCAGGGGACCAGGGACCAGAGCCCTGGCCTGCCCTG T C AKT2 Ensembl:ENSG00000105221 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1210243851 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8487853 26636 RMVar_ID_26636 Human_SNP_ID_665759913 A-to-I Human chr19 - 40275891 40275891 40275891 TCTCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCGCCTACCACCACGCCTGGCTAATTTTT TCTCTGCCTCAGCCTCCCGAGTAGCTGGGATTGCAGGCGCCTACCACCACGCCTGGCTAATTTTT T C AKT2 Ensembl:ENSG00000105221 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs187527820 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77340,RMVar_hsa_circ_194841,RMVar_hsa_circ_23550 26637 RMVar_ID_26637 Human_SNP_ID_665760197 A-to-I Human chr19 - 40276824 40276824 40276824 TCAGTAGAGATGGGAGTCTCCCTATTTTGCTCAGGCTGATCTTGAACTTTTGGGCTCCAGTGATC TCAGTAGAGATGGGAGTCTCCCTATTTTGCTCGGGCTGATCTTGAACTTTTGGGCTCCAGTGATC T C AKT2 Ensembl:ENSG00000105221 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs906429278 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77340,RMVar_hsa_circ_194841,RMVar_hsa_circ_23550 26638 RMVar_ID_26638 Human_SNP_ID_665760213 A-to-I Human chr19 - 40276901 40276901 40276901 CTCCCACCTCAGCCTTCTGAGTAGCTGGGACTACAGGCATGCACCATCATACCTGGCTAATTTTT CTCCCACCTCAGCCTTCTGAGTAGCTGGGACTGCAGGCATGCACCATCATACCTGGCTAATTTTT T C AKT2 Ensembl:ENSG00000105221 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1365036335 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77340,RMVar_hsa_circ_194841,RMVar_hsa_circ_23550 26639 RMVar_ID_26639 Human_SNP_ID_665762017 A-to-I Human chr19 - 40284063 40284063 40284063 CAATGGGCTGCTTTTCAACTTCATCCACTCCTACCTTCCCAGAGAAGCAGCAGGAGTTCACTCGT CAATGGGCTGCTTTTCAACTTCATCCACTCCTGCCTTCCCAGAGAAGCAGCAGGAGTTCACTCGT T C AKT2 Ensembl:ENSG00000105221 Protein coding intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1242028643 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4529505,Human_RBP_ID_5499596,Human_RBP_ID_6764404,Human_RBP_ID_8097499,Human_RBP_ID_8487951,Human_RBP_ID_9088057,Human_RBP_ID_17269313,Human_RBP_ID_17925376,Human_RBP_ID_23278465 26640 RMVar_ID_26640 Human_SNP_ID_665766746 A-to-I Human chr19 - 40302404 40302404 40302404 CAAAAAAATTAGACATGTTCGTGCATGCCTGTAGTCCCAACTACTCAGGAGGCTGACCTCAGAAG CAAAAAAATTAGACATGTTCGTGCATGCCTGTTGTCCCAACTACTCAGGAGGCTGACCTCAGAAG T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs963398828 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1565775,Human_RBP_ID_13458022 26641 RMVar_ID_26641 Human_SNP_ID_665766747 A-to-I Human chr19 - 40302404 40302404 40302404 CAAAAAAATTAGACATGTTCGTGCATGCCTGTAGTCCCAACTACTCAGGAGGCTGACCTCAGAAG CAAAAAAATTAGACATGTTCGTGCATGCCTGTGGTCCCAACTACTCAGGAGGCTGACCTCAGAAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs963398828 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1565775,Human_RBP_ID_13458022 26642 RMVar_ID_26642 Human_SNP_ID_665768225 A-to-I Human chr19 - 40308293 40308293 40308293 AAATTAGCCGGGTGTGGTGACACGCGCCTGTAATCCCAGCTACTCTGGAGGCTGAGGCAGGACAA AAATTAGCCGGGTGTGGTGACACGCGCCTGTAGTCCCAGCTACTCTGGAGGCTGAGGCAGGACAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs927099072 Functional Loss SNV dbSNP153 33..33 33 - - - 26643 RMVar_ID_26643 Human_SNP_ID_665769202 A-to-I Human chr19 - 40312291 40312291 40312291 CGACCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCATGCCCAGCCCTGTATG CGACCGCCTCGGCCTCCCAAAGTGCTGGGATTGCAGGCGTGAGCCACCATGCCCAGCCCTGTATG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941986878 Functional Loss SNV dbSNP153 33..33 33 - - - 26644 RMVar_ID_26644 Human_SNP_ID_665769644 A-to-I Human chr19 - 40314243 40314243 40314243 TTGTATTTTTAATAGAGATGGGGTTTCATCATATTGTTCAGGCTGGTCTTGAACTTCTGACCTCA TTGTATTTTTAATAGAGATGGGGTTTCATCATGTTGTTCAGGCTGGTCTTGAACTTCTGACCTCA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs930254317 Functional Loss SNV dbSNP153 33..33 33 - - - 26645 RMVar_ID_26645 Human_SNP_ID_665769957 A-to-I Human chr19 - 40315693 40315693 40315693 TCACTGTAGCCTGCGTCTGCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTGAGTGGCTGGGA TCACTGTAGCCTGCGTCTGCCGGGTTCAAGCATTTCTCCTGCCTCAGCCTCCTGAGTGGCTGGGA T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs908398697 Functional Loss SNV dbSNP153 33..33 33 - - - 26646 RMVar_ID_26646 Human_SNP_ID_665769958 A-to-I Human chr19 - 40315693 40315693 40315693 TCACTGTAGCCTGCGTCTGCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTGAGTGGCTGGGA TCACTGTAGCCTGCGTCTGCCGGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCTGAGTGGCTGGGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs908398697 Functional Loss SNV dbSNP153 33..33 33 - - - 26647 RMVar_ID_26647 Human_SNP_ID_665770565 A-to-I Human chr19 - 40318121 40318121 40318121 CACCGGCCTCCCAAAGTGCTGGGATTACAGACATGAGCCACTGCACCCAGCCACCTGGGCTGCCT CACCGGCCTCCCAAAGTGCTGGGATTACAGACGTGAGCCACTGCACCCAGCCACCTGGGCTGCCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1471616207 Functional Loss SNV dbSNP153 33..33 33 - - - 26648 RMVar_ID_26648 Human_SNP_ID_665770792 A-to-I Human chr19 - 40319183 40319183 40319183 TCACTGAAACCTCCACCTCCAGGGTTCCAGCTATTCTCCTGCCTCAGCCTCCCTGGTAGCTGGGA TCACTGAAACCTCCACCTCCAGGGTTCCAGCTGTTCTCCTGCCTCAGCCTCCCTGGTAGCTGGGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1014253095 Functional Loss SNV dbSNP153 33..33 33 - - - 26649 RMVar_ID_26649 Human_SNP_ID_665770808 A-to-I Human chr19 - 40319231 40319231 40319231 AGTTTTGCTCTTGTTGCCCAGGCTGGAGGACAATGTCATGATCTTGGCTCACTGAAACCTCCACC AGTTTTGCTCTTGTTGCCCAGGCTGGAGGACAGTGTCATGATCTTGGCTCACTGAAACCTCCACC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs563388717 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9922442 26650 RMVar_ID_26650 Human_SNP_ID_665770913 A-to-I Human chr19 - 40319675 40319675 40319675 AAATTAGCCGGGTGTGGTGACAGGTGCCTGTAATCCCGGCTACTTAGGAGGCTGAGGCAGGAGGA AAATTAGCCGGGTGTGGTGACAGGTGCCTGTAGTCCCGGCTACTTAGGAGGCTGAGGCAGGAGGA T C C19orf47 Ensembl:ENSG00000160392 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1020892833 Functional Loss SNV dbSNP153 33..33 33 - - - 26651 RMVar_ID_26651 Human_SNP_ID_665773544 A-to-I Human chr19 - 40329376 40329376 40329376 TCAGCCTCCTGAGTATCTGGGACTACAGGCACATGCCACCATGCCTGGCTGATTTTTTGTATTTT TCAGCCTCCTGAGTATCTGGGACTACAGGCACGTGCCACCATGCCTGGCTGATTTTTTGTATTTT T C C19orf47 Ensembl:ENSG00000160392 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7248338 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2626,GWAS_ID_2627,GWAS_ID_2628,GWAS_ID_2629,GWAS_ID_2630,GWAS_ID_2631,GWAS_ID_2632,GWAS_ID_2633,GWAS_ID_2634,GWAS_ID_2635,GWAS_ID_2636,GWAS_ID_2637,GWAS_ID_2638,GWAS_ID_2639,GWAS_ID_2640,GWAS_ID_2641,GWAS_ID_2642,GWAS_ID_2643,GWAS_ID_2644,GWAS_ID_2645,GWAS_ID_2646,GWAS_ID_2647,GWAS_ID_2648,GWAS_ID_2649,GWAS_ID_2650,GWAS_ID_2651,GWAS_ID_2652,GWAS_ID_2653,GWAS_ID_2654,GWAS_ID_2655,GWAS_ID_2656,GWAS_ID_2657,GWAS_ID_2658,GWAS_ID_2659,GWAS_ID_2660,GWAS_ID_2661,GWAS_ID_2662,GWAS_ID_2663,GWAS_ID_2664,GWAS_ID_2665,GWAS_ID_2666,GWAS_ID_2667,GWAS_ID_2668,GWAS_ID_2669,GWAS_ID_2670,GWAS_ID_2671,GWAS_ID_2672,GWAS_ID_2673,GWAS_ID_2674,GWAS_ID_2675,GWAS_ID_2676,GWAS_ID_2677,GWAS_ID_2678,GWAS_ID_2679,GWAS_ID_2680,GWAS_ID_2681,GWAS_ID_2682,GWAS_ID_2683,GWAS_ID_2684,GWAS_ID_2685,GWAS_ID_2686,GWAS_ID_2687,GWAS_ID_2688,GWAS_ID_2689,GWAS_ID_2690,GWAS_ID_2691,GWAS_ID_2692,GWAS_ID_2693,GWAS_ID_2694,GWAS_ID_2695,GWAS_ID_2696,GWAS_ID_2697,GWAS_ID_2698,GWAS_ID_2699,GWAS_ID_2700,GWAS_ID_2701,GWAS_ID_2702,GWAS_ID_2703,GWAS_ID_2704,GWAS_ID_2705,GWAS_ID_2706,GWAS_ID_2707,GWAS_ID_2708,GWAS_ID_2709,GWAS_ID_2710,GWAS_ID_2711,GWAS_ID_2712,GWAS_ID_2713,GWAS_ID_2714,GWAS_ID_2715,GWAS_ID_2716,GWAS_ID_2717,GWAS_ID_2718,GWAS_ID_2719,GWAS_ID_2720,GWAS_ID_2721,GWAS_ID_2722,GWAS_ID_2723,GWAS_ID_2724,GWAS_ID_2725,GWAS_ID_2726,GWAS_ID_2727,GWAS_ID_2728,GWAS_ID_2729,GWAS_ID_2730,GWAS_ID_2731,GWAS_ID_2732,GWAS_ID_2733,GWAS_ID_2734,GWAS_ID_2735,GWAS_ID_2736,GWAS_ID_2737,GWAS_ID_2738,GWAS_ID_2739,GWAS_ID_2740,GWAS_ID_2741,GWAS_ID_2742,GWAS_ID_2743,GWAS_ID_2744,GWAS_ID_2745,GWAS_ID_2746,GWAS_ID_2747,GWAS_ID_2748,GWAS_ID_2749,GWAS_ID_2750,GWAS_ID_2751,GWAS_ID_2752,GWAS_ID_2753,GWAS_ID_2754,GWAS_ID_2755,GWAS_ID_2756,GWAS_ID_2757,GWAS_ID_2758,GWAS_ID_2759,GWAS_ID_2760,GWAS_ID_2761,GWAS_ID_2762 RMVar_hsa_circ_15991,RMVar_hsa_circ_49324,RMVar_hsa_circ_6369 26652 RMVar_ID_26652 Human_SNP_ID_665777440 A-to-I Human chr19 - 40343907 40343907 40343907 CCTGTGGTCCCAGCTGCTCGGGAGGCTGAGGCAGGAGAACCGCTTGAACCCAGGAGGCGAAGGTT CCTGTGGTCCCAGCTGCTCGGGAGGCTGAGGCTGGAGAACCGCTTGAACCCAGGAGGCGAAGGTT T A C19orf47 Ensembl:ENSG00000160392 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1051093553 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_140359 26653 RMVar_ID_26653 Human_SNP_ID_665777441 A-to-I Human chr19 - 40343907 40343907 40343907 CCTGTGGTCCCAGCTGCTCGGGAGGCTGAGGCAGGAGAACCGCTTGAACCCAGGAGGCGAAGGTT CCTGTGGTCCCAGCTGCTCGGGAGGCTGAGGCGGGAGAACCGCTTGAACCCAGGAGGCGAAGGTT T C C19orf47 Ensembl:ENSG00000160392 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1051093553 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_140359 26654 RMVar_ID_26654 Human_SNP_ID_665779481 A-to-I Human chr19 + 40350651 40350651 40350651 CTAAAATCTGAGCAACTCGGGAGGCTGAGGTGAGAGGATTGCTTGAACCCAGGAGGCGGAGGCTG CTAAAATCTGAGCAACTCGGGAGGCTGAGGTGTGAGGATTGCTTGAACCCAGGAGGCGGAGGCTG A T PLD3 Ensembl:ENSG00000105223 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1316906503 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266679 26655 RMVar_ID_26655 Human_SNP_ID_665779654 A-to-I Human chr19 + 40351408 40351408 40351408 TCTACTAAAATTACAAAAAATTAGGCAGGCATAGTGGCAGACACCTGTAATCCCAGCTATTCAGG TCTACTAAAATTACAAAAAATTAGGCAGGCATGGTGGCAGACACCTGTAATCCCAGCTATTCAGG A G PLD3 Ensembl:ENSG00000105223 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1209685788 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266679 26656 RMVar_ID_26656 Human_SNP_ID_665779979 A-to-I Human chr19 + 40352707 40352707 40352707 CTTTGAGGCCAGGCACAGTGGCTTATGCCTGTAATCCCAGCACTTTGAGAGGTTGAGGTAGGCAG CTTTGAGGCCAGGCACAGTGGCTTATGCCTGTGATCCCAGCACTTTGAGAGGTTGAGGTAGGCAG A G PLD3 Ensembl:ENSG00000105223 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1407789589 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17568596 RMVar_hsa_circ_266679 26657 RMVar_ID_26657 Human_SNP_ID_665780096 A-to-I Human chr19 + 40353269 40353269 40353269 CTGGCCAATATGGTGAAACACTGTCTTTACAAAAAATACAAAAATTAGCCAGGTGTGGTGGCGGG CTGGCCAATATGGTGAAACACTGTCTTTACAACAAATACAAAAATTAGCCAGGTGTGGTGGCGGG A C PLD3 Ensembl:ENSG00000105223 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs939735464 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266679 26658 RMVar_ID_26658 Human_SNP_ID_665780098 A-to-I Human chr19 + 40353274 40353274 40353274 CAATATGGTGAAACACTGTCTTTACAAAAAATACAAAAATTAGCCAGGTGTGGTGGCGGGCACCT CAATATGGTGAAACACTGTCTTTACAAAAAATGCAAAAATTAGCCAGGTGTGGTGGCGGGCACCT A G PLD3 Ensembl:ENSG00000105223 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1443981183 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23309649,Human_RBP_ID_25417869 RMVar_hsa_circ_266679 26659 RMVar_ID_26659 Human_SNP_ID_665780110 A-to-I Human chr19 + 40353323 40353323 40353323 GTGGTGGCGGGCACCTGTCATCCCACCTACTCAGGAGGTTGAGACATGAGAATCACTTGAACCTG GTGGTGGCGGGCACCTGTCATCCCACCTACTCGGGAGGTTGAGACATGAGAATCACTTGAACCTG A G PLD3 Ensembl:ENSG00000105223 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1406389255 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266679 26660 RMVar_ID_26660 Human_SNP_ID_665780291 A-to-I Human chr19 + 40354011 40354011 40354011 AAGCTCCCAGGCTCAAGCCATCCTCTTGCTTCAGCCTCCCACGTAGCTAGGGCTACAGGCGCATA AAGCTCCCAGGCTCAAGCCATCCTCTTGCTTCGGCCTCCCACGTAGCTAGGGCTACAGGCGCATA A G PLD3 Ensembl:ENSG00000105223 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1229189744 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266679 26661 RMVar_ID_26661 Human_SNP_ID_665780420 A-to-I Human chr19 + 40354406 40354406 40354406 GGCTTTTTATTTTTCTGTAGAGACAAGATCTCACTTTGTTGCCCAGGCTGCCCAGGTCTCAAACT GGCTTTTTATTTTTCTGTAGAGACAAGATCTCGCTTTGTTGCCCAGGCTGCCCAGGTCTCAAACT A G PLD3 Ensembl:ENSG00000105223 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs538769237 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13458590,Human_RBP_ID_23178385 RMVar_hsa_circ_266679 26662 RMVar_ID_26662 Human_SNP_ID_665780712 A-to-I Human chr19 + 40355493 40355484 40355493 CGCCACCAGGGCCTGGCTGATTTTGTATTTTTAGTAGAGACGGGTTTCTCCATGTTGGCCAGGCT CGCCACCAGGGCCTGGCTGATTTT_________GTAGAGACGGGTTTCTCCATGTTGGCCAGGCT TGTATTTTTA T PLD3 Ensembl:ENSG00000105223 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1368799090 Functional Loss DEL dbSNP153 25..33 33 - - - RMVar_hsa_circ_266679 26663 RMVar_ID_26663 Human_SNP_ID_665782412 A-to-I Human chr19 + 40362973 40362973 40362973 TTCTTGTAGAGACTGGGCCTTGCTATGTTGCCAAGGCTAGTCTGGAACTCCTGGGCTCAAGCAGT TTCTTGTAGAGACTGGGCCTTGCTATGTTGCCCAGGCTAGTCTGGAACTCCTGGGCTCAAGCAGT A C PLD3 Ensembl:ENSG00000105223 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1321988685 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13458780 RMVar_hsa_circ_266679 26664 RMVar_ID_26664 Human_SNP_ID_665782413 A-to-I Human chr19 + 40362973 40362973 40362973 TTCTTGTAGAGACTGGGCCTTGCTATGTTGCCAAGGCTAGTCTGGAACTCCTGGGCTCAAGCAGT TTCTTGTAGAGACTGGGCCTTGCTATGTTGCCGAGGCTAGTCTGGAACTCCTGGGCTCAAGCAGT A G PLD3 Ensembl:ENSG00000105223 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1321988685 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13458780 RMVar_hsa_circ_266679 26665 RMVar_ID_26665 Human_SNP_ID_665782755 A-to-I Human chr19 + 40364243 40364243 40364243 GGTCGTGGTGGCAGGCGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAA GGTCGTGGTGGCAGGCGCCTGTAATCCCAGCTGCTCGGGAGGCTGAGGCAGGAGAATCGCTTGAA A G PLD3 Ensembl:ENSG00000105223 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1402630646 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266679 26666 RMVar_ID_26666 Human_SNP_ID_665794019 A-to-I Human chr19 - 40400115 40400115 40400115 AGCTGGGTGTGGTGGTGCATGCCTGTGGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGGGTCGCT AGCTGGGTGTGGTGGTGCATGCCTGTGGTCCCTGCTACTCAGGAGGCTGAGGCAGGAGGGTCGCT T A PRX Ensembl:ENSG00000105227 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs576121617 Functional Loss SNV dbSNP153 33..33 33 - - - 26667 RMVar_ID_26667 Human_SNP_ID_665808924 A-to-I Human chr19 - 40452630 40452630 40452630 GAACTCCTAACCTCAGGCGATCTGGCCTCCTCAGTCTCCCAAAGTGCTGGGATTACAGGGGTTAG GAACTCCTAACCTCAGGCGATCTGGCCTCCTCGGTCTCCCAAAGTGCTGGGATTACAGGGGTTAG T C BLVRB Ensembl:ENSG00000090013 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs562306626 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_194862,RMVar_hsa_circ_126796,RMVar_hsa_circ_345649 26668 RMVar_ID_26668 Human_SNP_ID_665809262 A-to-I Human chr19 - 40453978 40453978 40453978 AAACTATTTATTTATTTCTTTTTGTTGAGACAAGGTCTTGCTCTGTTGTCCAGGCTGGAGTGCAG AAACTATTTATTTATTTCTTTTTGTTGAGACAGGGTCTTGCTCTGTTGTCCAGGCTGGAGTGCAG T C BLVRB Ensembl:ENSG00000090013 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs911785500 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_194862,RMVar_hsa_circ_126796,RMVar_hsa_circ_345649 26669 RMVar_ID_26669 Human_SNP_ID_665809282 A-to-I Human chr19 - 40454076 40454076 40454076 CCATCTAATTTTTAAAATTTTTTTGTTGCGACAGAGTCTGGCTTTGTTGCCCAGGCTGGTCTCTG CCATCTAATTTTTAAAATTTTTTTGTTGCGACGGAGTCTGGCTTTGTTGCCCAGGCTGGTCTCTG T C BLVRB Ensembl:ENSG00000090013 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1237057466 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_194862,RMVar_hsa_circ_126796,RMVar_hsa_circ_345649 26670 RMVar_ID_26670 Human_SNP_ID_665810050 A-to-I Human chr19 - 40457427 40457427 40457427 TAGAGACAGGGTTTCGCCATGTTGGCCAGGCTAGTCTCGAACTCCTGACCTCAAGTGTGTTTCAT TAGAGACAGGGTTTCGCCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAAGTGTGTTTCAT T C BLVRB Ensembl:ENSG00000090013 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1314213119 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_194862,RMVar_hsa_circ_126796,RMVar_hsa_circ_345649 26671 RMVar_ID_26671 Human_SNP_ID_665810629 A-to-I Human chr19 - 40459194 40459194 40459194 TTCCCAAGTACTTGGGATTACAGGTATGTGCCACCATGCCTGGCTAATTTTGTATTTTTAGTGGC TTCCCAAGTACTTGGGATTACAGGTATGTGCCGCCATGCCTGGCTAATTTTGTATTTTTAGTGGC T C BLVRB Ensembl:ENSG00000090013 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs527409957 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_194862,RMVar_hsa_circ_126796 26672 RMVar_ID_26672 Human_SNP_ID_665811546 A-to-I Human chr19 - 40462419 40462419 40462419 AAAAAATTCGCCGGGTGTTGTGGTGCACACCTATAATCCCAGCTACTCTGGAGGCTGAGGTGGGA AAAAAATTCGCCGGGTGTTGTGGTGCACACCTGTAATCCCAGCTACTCTGGAGGCTGAGGTGGGA T C BLVRB Ensembl:ENSG00000090013 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1374911516 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_194862,RMVar_hsa_circ_126796 26673 RMVar_ID_26673 Human_SNP_ID_665824830 A-to-I Human chr19 - 40512979 40512979 40512979 AGGTGCACGGTGTCTGCTCCCGGGCCGACGGCACCGCCGGCCGCAACCAGCTCCTCGCCACACCG AGGTGCACGGTGTCTGCTCCCGGGCCGACGGCGCCGCCGGCCGCAACCAGCTCCTCGCCACACCG T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs563121072 Functional Loss SNV dbSNP153 33..33 33 - - - 26674 RMVar_ID_26674 Human_SNP_ID_665830908 A-to-I Human chr19 + 40536479 40536479 40536479 CAGGTGATTCACCCGCCTTGGCCTCCCAAAGTACTAGGATTACAGGTGTGAGCCACTGTGCCCGG CAGGTGATTCACCCGCCTTGGCCTCCCAAAGTGCTAGGATTACAGGTGTGAGCCACTGTGCCCGG A G SPTBN4 Ensembl:ENSG00000160460 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1258597625 Functional Loss SNV dbSNP153 33..33 33 - - - 26675 RMVar_ID_26675 Human_SNP_ID_665832564 A-to-I Human chr19 + 40543189 40543189 40543189 AATGGGGAGAGTGGCCGGGCACAGTGGCTCACACCTGTAATCCCACACTTTAGGAGGCCAAGATG AATGGGGAGAGTGGCCGGGCACAGTGGCTCACGCCTGTAATCCCACACTTTAGGAGGCCAAGATG A G SPTBN4 Ensembl:ENSG00000160460 Protein coding intron GSE107867 ASD brains,cerebellum;ASD brains,Fragile X samples from NIH NeuroBioBank;ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs902473661 Functional Loss SNV dbSNP153 33..33 33 - - - 26676 RMVar_ID_26676 Human_SNP_ID_665836401 A-to-I Human chr19 + 40557833 40557833 40557833 CCAGCTACTTGGGAGGCTGAGGCAGGAGAATCACTTGAACCCGGGAGGAGGAGGTTGCAGTGAGC CCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGGGAGGAGGAGGTTGCAGTGAGC A G SPTBN4 Ensembl:ENSG00000160460 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs996747955 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_194871 26677 RMVar_ID_26677 Human_SNP_ID_665867918 A-to-I Human chr19 + 40667079 40667079 40667079 TTTGGGGTGGGCACTGGTGTGGGGCCCAGGAGAGCCCCTAAGCAAGTGTCCCCCCTCCATCCTGT TTTGGGGTGGGCACTGGTGTGGGGCCCAGGAGGGCCCCTAAGCAAGTGTCCCCCCTCCATCCTGT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs373596094 Functional Loss SNV dbSNP153 33..33 33 - - - 26678 RMVar_ID_26678 Human_SNP_ID_665878619 A-to-I Human chr19 - 40705830 40705824 40705830 AACCTCCAGGGCTCAAGCAATCCTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCACATG AACCTCCAGGGCTCAAGCAATCCTCCTGCCTC______CTGAGTAGCTGGGACTACAGGCACATG GGAGGCT G COQ8B Ensembl:ENSG00000123815 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1568441264 Functional Loss DEL dbSNP153 33..38 33 - - - RMVar_hsa_circ_194908,RMVar_hsa_circ_84628,RMVar_hsa_circ_330581 26679 RMVar_ID_26679 Human_SNP_ID_665879002 A-to-I Human chr19 - 40707518 40707518 40707518 TGAACCGGGGAGGCGGAGGTTGCAGTGAACCAAGATCATGCCATTGTACTCCAGCCTTGGAGACA TGAACCGGGGAGGCGGAGGTTGCAGTGAACCACGATCATGCCATTGTACTCCAGCCTTGGAGACA T G COQ8B Ensembl:ENSG00000123815 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1300922067 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_194908,RMVar_hsa_circ_84628,RMVar_hsa_circ_330581 26680 RMVar_ID_26680 Human_SNP_ID_665883678 A-to-I Human chr19 + 40724854 40724854 40724854 ACCTGTAGTCCCAGCTACTCGGAGGGTGAGGCAGGAGGATCACTTGAACCTCGGAGGCAGAGGTT ACCTGTAGTCCCAGCTACTCGGAGGGTGAGGCGGGAGGATCACTTGAACCTCGGAGGCAGAGGTT A G ITPKC Ensembl:ENSG00000086544 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1475303646 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121327,RMVar_hsa_circ_194911 26681 RMVar_ID_26681 Human_SNP_ID_665891777 A-to-I Human chr19 + 40753265 40753265 40753265 CAGTCCCAGCTACTCGGGAGGCTGAGCAGGAGAATCACTTGAACCCTGGGAAGCAGAGGTCGCAG CAGTCCCAGCTACTCGGGAGGCTGAGCAGGAGGATCACTTGAACCCTGGGAAGCAGAGGTCGCAG A G SNRPA Ensembl:ENSG00000077312 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1043004055 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91364,RMVar_hsa_circ_194923 26682 RMVar_ID_26682 Human_SNP_ID_665892029 A-to-I Human chr19 + 40753818 40753818 40753818 AATCTTATTTTATTTATTTATTTATTTTTGAGACGGAGTCTTCCTCTGTCGCCCAGGCTGGAGTG AATCTTATTTTATTTATTTATTTATTTTTGAGGCGGAGTCTTCCTCTGTCGCCCAGGCTGGAGTG A G SNRPA Ensembl:ENSG00000077312 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1434592412 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91364,RMVar_hsa_circ_194923 26683 RMVar_ID_26683 Human_SNP_ID_665892095 A-to-I Human chr19 + 40753999 40753999 40753999 AATTTTTTGTATATTTAGTAGAGAAGGGGTTTAACCATGTTAGCCAGGATGGTGTTGATTTCCTG AATTTTTTGTATATTTAGTAGAGAAGGGGTTTCACCATGTTAGCCAGGATGGTGTTGATTTCCTG A C SNRPA Ensembl:ENSG00000077312 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1188897855 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91364,RMVar_hsa_circ_194923 26684 RMVar_ID_26684 Human_SNP_ID_665892096 A-to-I Human chr19 + 40753999 40753999 40753999 AATTTTTTGTATATTTAGTAGAGAAGGGGTTTAACCATGTTAGCCAGGATGGTGTTGATTTCCTG AATTTTTTGTATATTTAGTAGAGAAGGGGTTTTACCATGTTAGCCAGGATGGTGTTGATTTCCTG A T SNRPA Ensembl:ENSG00000077312 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1188897855 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91364,RMVar_hsa_circ_194923 26685 RMVar_ID_26685 Human_SNP_ID_665892100 A-to-I Human chr19 + 40754008 40754008 40754008 TATATTTAGTAGAGAAGGGGTTTAACCATGTTAGCCAGGATGGTGTTGATTTCCTGACCTCGTGA TATATTTAGTAGAGAAGGGGTTTAACCATGTTGGCCAGGATGGTGTTGATTTCCTGACCTCGTGA A G SNRPA Ensembl:ENSG00000077312 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1333316624 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91364,RMVar_hsa_circ_194923 26686 RMVar_ID_26686 Human_SNP_ID_665892236 A-to-I Human chr19 + 40754343 40754343 40754343 TATGCTGGTCTCGAACTCCTGAACTGTGATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTAC TATGCTGGTCTCGAACTCCTGAACTGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTAC A G SNRPA Ensembl:ENSG00000077312 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277198866 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13459793 RMVar_hsa_circ_91364,RMVar_hsa_circ_194923 26687 RMVar_ID_26687 Human_SNP_ID_665892575 A-to-I Human chr19 + 40755541 40755541 40755541 TGACCACAAGGCATGCACCACTATGCCTGGCTAATTTTTGTATCTTTTGTAGAGACAGGGTTTCA TGACCACAAGGCATGCACCACTATGCCTGGCTGATTTTTGTATCTTTTGTAGAGACAGGGTTTCA A G SNRPA Ensembl:ENSG00000077312 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs958215441 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91364,RMVar_hsa_circ_194923 26688 RMVar_ID_26688 Human_SNP_ID_665892583 A-to-I Human chr19 + 40755578 40755578 40755578 TTGTATCTTTTGTAGAGACAGGGTTTCACCCTATTGCCCAGACTGGTCTTGAACTCTTGAGTGCA TTGTATCTTTTGTAGAGACAGGGTTTCACCCTGTTGCCCAGACTGGTCTTGAACTCTTGAGTGCA A G SNRPA Ensembl:ENSG00000077312 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs750132048 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13459828 RMVar_hsa_circ_91364,RMVar_hsa_circ_194923 26689 RMVar_ID_26689 Human_SNP_ID_665893194 A-to-I Human chr19 + 40757847 40757847 40757847 ACCTGTAGTCCCAGCTACTCCTGTGGCTGAGGAAGGAGAATTGCTTGAACCCGGGAGGCAGAGAT ACCTGTAGTCCCAGCTACTCCTGTGGCTGAGGCAGGAGAATTGCTTGAACCCGGGAGGCAGAGAT A C SNRPA Ensembl:ENSG00000077312 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs949382923 Functional Loss SNV dbSNP153 33..33 33 - - - 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 26690 RMVar_ID_26690 Human_SNP_ID_665895498 A-to-I Human chr19 + 40766256 40766256 40766256 GAAAGGGAGATTGGGCAGGGTGGCTCACGCCTATAATCCCAGCACCTTGGGAGGCCGAGGTGGGC GAAAGGGAGATTGGGCAGGGTGGCTCACGCCTGTAATCCCAGCACCTTGGGAGGCCGAGGTGGGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1466851962 Functional Loss SNV dbSNP153 33..33 33 - - - 26691 RMVar_ID_26691 Human_SNP_ID_665895499 A-to-I Human chr19 + 40766258 40766257 40766259 AAGGGAGATTGGGCAGGGTGGCTCACGCCTATAATCCCAGCACCTTGGGAGGCCGAGGTGGGCAG AAGGGAGATTGGGCAGGGTGGCTCACGCCTAT__TCCCAGCACCTTGGGAGGCCGAGGTGGGCAG TAA T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1568486727 Functional Loss DEL dbSNP153 33..34 33 - - - 26692 RMVar_ID_26692 Human_SNP_ID_665898265 A-to-I Human chr19 + 40776287 40776287 40776287 GACCTCATGATCTGCCCGCCTTGGCCTCCCGGAGTGCTGGGATTACAGGTGTGAGCCACTGCCCC GACCTCATGATCTGCCCGCCTTGGCCTCCCGGGGTGCTGGGATTACAGGTGTGAGCCACTGCCCC A G MIA,MIA-RAB4B Ensembl:ENSG00000261857,Ensembl:ENSG00000268975 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928000569 Functional Loss SNV dbSNP153 33..33 33 - - - 26693 RMVar_ID_26693 Human_SNP_ID_665899397 A-to-I Human chr19 - 40780333 40780333 40780333 AAGGGGCAGTACAGGGAGAGAGGAGACAGCTCAGAGGATCCCCCATCCTCCAAGGCCCTCTCAGT AAGGGGCAGTACAGGGAGAGAGGAGACAGCTCGGAGGATCCCCCATCCTCCAAGGCCCTCTCAGT T C AC008537.4 Ensembl:ENSG00000282951 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs572474490 Functional Loss SNV dbSNP153 33..33 33 - - - 26694 RMVar_ID_26694 Human_SNP_ID_665899522 A-to-I Human chr19 - 40780674 40780674 40780674 GCCCCTACCTCTTTTTCTTCCACCATCTCTTTATCTCTCCAGTACTCCCTCTCTCCTTGGATATA GCCCCTACCTCTTTTTCTTCCACCATCTCTTTGTCTCTCCAGTACTCCCTCTCTCCTTGGATATA T C AC008537.4 Ensembl:ENSG00000282951 lincRNA intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs535051038 Functional Loss SNV dbSNP153 33..33 33 - - - 26695 RMVar_ID_26695 Human_SNP_ID_665899523 A-to-I Human chr19 - 40780674 40780674 40780674 GCCCCTACCTCTTTTTCTTCCACCATCTCTTTATCTCTCCAGTACTCCCTCTCTCCTTGGATATA GCCCCTACCTCTTTTTCTTCCACCATCTCTTTCTCTCTCCAGTACTCCCTCTCTCCTTGGATATA T G AC008537.4 Ensembl:ENSG00000282951 lincRNA intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs535051038 Functional Loss SNV dbSNP153 33..33 33 - - - 26696 RMVar_ID_26696 Human_SNP_ID_665912881 A-to-I Human chr19 + 40825780 40825780 40825780 GTATGTATGTGTTGTAGAGACTGGGTCTTACTATATTGTCCAGGCTGGTCTCGAACTCCTGGACT GTATGTATGTGTTGTAGAGACTGGGTCTTACTCTATTGTCCAGGCTGGTCTCGAACTCCTGGACT A C AC008537.1 Ensembl:ENSG00000268797 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs890438927 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5650199 26697 RMVar_ID_26697 Human_SNP_ID_665913338 A-to-I Human chr19 + 40827561 40827561 40827561 TCGCTCCGTCGCCCATGCTGGAGTGCGGTGGCACGATCTCAGTTCACTGCAACGTCTGCCTCCCA TCGCTCCGTCGCCCATGCTGGAGTGCGGTGGCGCGATCTCAGTTCACTGCAACGTCTGCCTCCCA A G AC008537.1 Ensembl:ENSG00000268797 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982985441 Functional Loss SNV dbSNP153 33..33 33 - - - 26698 RMVar_ID_26698 Human_SNP_ID_665913414 A-to-I Human chr19 + 40827856 40827856 40827856 GTCGCCCAGGCCGGTTTCGAATTCCTGAGCTCAAGTGATCCACCACCTTGGCCTCCCAAAGTGCT GTCGCCCAGGCCGGTTTCGAATTCCTGAGCTCCAGTGATCCACCACCTTGGCCTCCCAAAGTGCT A C AC008537.1 Ensembl:ENSG00000268797 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965412575 Functional Loss SNV dbSNP153 33..33 33 - - - 26699 RMVar_ID_26699 Human_SNP_ID_665913583 A-to-I Human chr19 + 40828582 40828582 40828582 AGAATGAGTTGAATGTGGTGGCACATGCCTGTAATCCCAGCTACTTGAGAAGCTAAGGCGGGAGA AGAATGAGTTGAATGTGGTGGCACATGCCTGTTATCCCAGCTACTTGAGAAGCTAAGGCGGGAGA A T AC008537.1 Ensembl:ENSG00000268797 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223817241 Functional Loss SNV dbSNP153 33..33 33 - - - 26700 RMVar_ID_26700 Human_SNP_ID_665913587 A-to-I Human chr19 + 40828604 40828604 40828604 ACATGCCTGTAATCCCAGCTACTTGAGAAGCTAAGGCGGGAGAATCAGTTGAGCTCAGGAGGTCA ACATGCCTGTAATCCCAGCTACTTGAGAAGCTGAGGCGGGAGAATCAGTTGAGCTCAGGAGGTCA A G AC008537.1 Ensembl:ENSG00000268797 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1479770829 Functional Loss SNV dbSNP153 33..33 33 - - - 26701 RMVar_ID_26701 Human_SNP_ID_665913818 A-to-I Human chr19 + 40829649 40829649 40829649 CTACTATGCCTGGCTAATTTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGACAGGC CTACTATGCCTGGCTAATTTTTTTGTATTTTTCGTAGAGACGGGGTTTCACCATGTTGGACAGGC A C AC008537.1 Ensembl:ENSG00000268797 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1050228326 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13460584,Human_RBP_ID_25419120 26702 RMVar_ID_26702 Human_SNP_ID_665913955 A-to-I Human chr19 + 40830271 40830271 40830271 AATTTTTTTTCTTTTTCTTTTAAGACCGTCTCACTCTGTCTTTCAGGCTGCAGTGCAGTAGGGCA AATTTTTTTTCTTTTTCTTTTAAGACCGTCTCGCTCTGTCTTTCAGGCTGCAGTGCAGTAGGGCA A G AC008537.1 Ensembl:ENSG00000268797 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs778302448 Functional Loss SNV dbSNP153 33..33 33 - - - 26703 RMVar_ID_26703 Human_SNP_ID_665913960 A-to-I Human chr19 + 40830298 40830298 40830298 GTCTCACTCTGTCTTTCAGGCTGCAGTGCAGTAGGGCAATCTTGGCTCACTGCGACCTCTGCCTC GTCTCACTCTGTCTTTCAGGCTGCAGTGCAGTGGGGCAATCTTGGCTCACTGCGACCTCTGCCTC A G AC008537.1 Ensembl:ENSG00000268797 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1272599119 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18733587 26704 RMVar_ID_26704 Human_SNP_ID_665914100 A-to-I Human chr19 + 40830941 40830941 40830941 CCTCCACTTTGTAAAAAGTCCCTCCATTGGCCAGGCGCGGCGGCTCACACCTGTAATCCCAGCAC CCTCCACTTTGTAAAAAGTCCCTCCATTGGCCGGGCGCGGCGGCTCACACCTGTAATCCCAGCAC A G AC008537.1 Ensembl:ENSG00000268797 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917090511 Functional Loss SNV dbSNP153 33..33 33 - - - 26705 RMVar_ID_26705 Human_SNP_ID_665914106 A-to-I Human chr19 + 40830957 40830957 40830957 AGTCCCTCCATTGGCCAGGCGCGGCGGCTCACACCTGTAATCCCAGCACTTTTGGAGGCCGAGGC AGTCCCTCCATTGGCCAGGCGCGGCGGCTCACGCCTGTAATCCCAGCACTTTTGGAGGCCGAGGC A G AC008537.1 Ensembl:ENSG00000268797 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1363800953 Functional Loss SNV dbSNP153 33..33 33 - - - 26706 RMVar_ID_26706 Human_SNP_ID_665915173 A-to-I Human chr19 + 40835264 40835264 40835264 TTGAACCTGGGAGGCGGAGGTTGCAGTGATCCATGATCCGGCCATTGCGCTCCAGCCTGGGTGAC TTGAACCTGGGAGGCGGAGGTTGCAGTGATCCGTGATCCGGCCATTGCGCTCCAGCCTGGGTGAC A G AC008537.1 Ensembl:ENSG00000268797 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984822492 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23178534,Human_RBP_ID_25419163 26707 RMVar_ID_26707 Human_SNP_ID_665915419 A-to-I Human chr19 + 40836316 40836316 40836316 GTTGGCCAGGCTGGTTTTGAACTCCTGACCTCAAGTGATCCACTCGCTTTGGCTTCACAAAGTGC GTTGGCCAGGCTGGTTTTGAACTCCTGACCTCCAGTGATCCACTCGCTTTGGCTTCACAAAGTGC A C AC008537.1 Ensembl:ENSG00000268797 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1448714340 Functional Loss SNV dbSNP153 33..33 33 - - - 26708 RMVar_ID_26708 Human_SNP_ID_665921672 A-to-I Human chr19 + 40855825 40855825 40855825 GGGACTATAGACGTGCACCACCATGCTGGGCTAATGTTTGTATTTTTAGTAGAGACAGGGTTTCA GGGACTATAGACGTGCACCACCATGCTGGGCTGATGTTTGTATTTTTAGTAGAGACAGGGTTTCA A G AC008537.1 Ensembl:ENSG00000268797 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs548784652 Functional Loss SNV dbSNP153 33..33 33 - - - 26709 RMVar_ID_26709 Human_SNP_ID_666009848 A-to-I Human chr19 - 41169760 41169760 41169760 ATTTTCGGCCGGTCGCGGTGGCTCATGCCTGTAATCCCAGCACCTTGGGAGGCCGAGGCGGGCGG ATTTTCGGCCGGTCGCGGTGGCTCATGCCTGTGATCCCAGCACCTTGGGAGGCCGAGGCGGGCGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006360626 Functional Loss SNV dbSNP153 33..33 33 - - - 26710 RMVar_ID_26710 Human_SNP_ID_666031723 A-to-I Human chr19 + 41246690 41246685 41246691 TGAGCTGAGATTATGCTACTGCACTCTAGCCTAGGCAACAGAGCGAGACTCGGTTTCAAAAAAAA TGAGCTGAGATTATGCTACTGCACTCTA______GCAACAGAGCGAGACTCGGTTTCAAAAAAAA AGCCTAG A AXL Ensembl:ENSG00000167601 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs200421249 Functional Loss DEL dbSNP153 29..34 33 - - - RMVar_hsa_circ_92315,RMVar_hsa_circ_82455,RMVar_hsa_circ_105188,RMVar_hsa_circ_194947,RMVar_hsa_circ_116275,RMVar_hsa_circ_27652,RMVar_hsa_circ_194949,RMVar_hsa_circ_126510,RMVar_hsa_circ_27272,RMVar_hsa_circ_194951,RMVar_hsa_circ_194950,RMVar_hsa_circ_116732,RMVar_hsa_circ_119243,RMVar_hsa_circ_194955,RMVar_hsa_circ_95173,RMVar_hsa_circ_50754,RMVar_hsa_circ_126089,RMVar_hsa_circ_194958,RMVar_hsa_circ_194959,RMVar_hsa_circ_103530,RMVar_hsa_circ_97203,RMVar_hsa_circ_194961,RMVar_hsa_circ_194960,RMVar_hsa_circ_88471,RMVar_hsa_circ_194964,RMVar_hsa_circ_194967,RMVar_hsa_circ_75546,RMVar_hsa_circ_194966,RMVar_hsa_circ_120828,RMVar_hsa_circ_78357,RMVar_hsa_circ_125058,RMVar_hsa_circ_194968,RMVar_hsa_circ_194969,RMVar_hsa_circ_194970,RMVar_hsa_circ_88940,RMVar_hsa_circ_369860,RMVar_hsa_circ_97084,RMVar_hsa_circ_194972,RMVar_hsa_circ_194973,RMVar_hsa_circ_347494,RMVar_hsa_circ_194971,RMVar_hsa_circ_319487,RMVar_hsa_circ_194975,RMVar_hsa_circ_194976,RMVar_hsa_circ_194974 26711 RMVar_ID_26711 Human_SNP_ID_666031885 A-to-I Human chr19 + 41247366 41247366 41247366 AGAAACCCCGTCTCTACTAAAAATACAAAATTAGCTGGGCGTAGTGGCACATGCCTGTACTTGGG AGAAACCCCGTCTCTACTAAAAATACAAAATTTGCTGGGCGTAGTGGCACATGCCTGTACTTGGG A T AXL Ensembl:ENSG00000167601 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs189028699 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92315,RMVar_hsa_circ_82455,RMVar_hsa_circ_105188,RMVar_hsa_circ_194947,RMVar_hsa_circ_116275,RMVar_hsa_circ_27652,RMVar_hsa_circ_194949,RMVar_hsa_circ_126510,RMVar_hsa_circ_27272,RMVar_hsa_circ_194951,RMVar_hsa_circ_194950,RMVar_hsa_circ_116732,RMVar_hsa_circ_119243,RMVar_hsa_circ_194955,RMVar_hsa_circ_95173,RMVar_hsa_circ_50754,RMVar_hsa_circ_126089,RMVar_hsa_circ_194958,RMVar_hsa_circ_194959,RMVar_hsa_circ_103530,RMVar_hsa_circ_97203,RMVar_hsa_circ_194961,RMVar_hsa_circ_194960,RMVar_hsa_circ_88471,RMVar_hsa_circ_194964,RMVar_hsa_circ_194967,RMVar_hsa_circ_75546,RMVar_hsa_circ_194966,RMVar_hsa_circ_120828,RMVar_hsa_circ_78357,RMVar_hsa_circ_125058,RMVar_hsa_circ_194968,RMVar_hsa_circ_194969,RMVar_hsa_circ_194970,RMVar_hsa_circ_88940,RMVar_hsa_circ_369860,RMVar_hsa_circ_97084,RMVar_hsa_circ_194972,RMVar_hsa_circ_194973,RMVar_hsa_circ_347494,RMVar_hsa_circ_194971,RMVar_hsa_circ_319487,RMVar_hsa_circ_194975,RMVar_hsa_circ_194976,RMVar_hsa_circ_194974 26712 RMVar_ID_26712 Human_SNP_ID_666037031 A-to-I Human chr19 + 41266493 41266493 41266493 CTTTTTTTTAAATACAGATGGGGGGTCTCGCTATGTTGCCCAGGGTGGTCTTGAACTCCTGGGTT CTTTTTTTTAAATACAGATGGGGGGTCTCGCTGTGTTGCCCAGGGTGGTCTTGAACTCCTGGGTT A G HNRNPUL1 Ensembl:ENSG00000105323 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1348403611 Functional Loss SNV dbSNP153 33..33 33 - - - 26713 RMVar_ID_26713 Human_SNP_ID_666048882 A-to-I Human chr19 - 41312865 41312865 41312865 TGAGGTAGGAGAATTGTTTGAACTCCGGAGGCAGAGGTTGCAGTGAACCGAGATCACGTACTCCA TGAGGTAGGAGAATTGTTTGAACTCCGGAGGCTGAGGTTGCAGTGAACCGAGATCACGTACTCCA T A TGFB1 Ensembl:ENSG00000105329 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1262260025 Functional Loss SNV dbSNP153 33..33 33 - - - 26714 RMVar_ID_26714 Human_SNP_ID_666049108 A-to-I Human chr19 + 41313723 41313722 41313724 GCTTTCCTGTTTTCTTTCCATTTTTTTGAGACAGAGTCTTCACTCTGTCACCCAGGCTGGAGTGC GCTTTCCTGTTTTCTTTCCATTTTTTTGAGAC__AGTCTTCACTCTGTCACCCAGGCTGGAGTGC CAG C CCDC97 Ensembl:ENSG00000142039 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1380337687 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_1190138 26715 RMVar_ID_26715 Human_SNP_ID_666049561 A-to-I Human chr19 + 41315425 41315425 41315425 GGTCAGGAGTTGGAGACCAGCCTAGCCAACATAGCGAAACCCTGTCTCTACTAAAAATACAAAAA GGTCAGGAGTTGGAGACCAGCCTAGCCAACATGGCGAAACCCTGTCTCTACTAAAAATACAAAAA A G CCDC97 Ensembl:ENSG00000142039 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1205086791 Functional Loss SNV dbSNP153 33..33 33 - - - 26716 RMVar_ID_26716 Human_SNP_ID_666055088 A-to-I Human chr19 - 41334293 41334293 41334293 TGGCTCACTGCAACCTCTGCTTCTTGGGTTCAAGCAGATTCTTGTGCCTCAGCCTCCTGAGTAGC TGGCTCACTGCAACCTCTGCTTCTTGGGTTCAGGCAGATTCTTGTGCCTCAGCCTCCTGAGTAGC T C TGFB1 Ensembl:ENSG00000105329 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs543982131 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_195011,RMVar_hsa_circ_105511,RMVar_hsa_circ_195012,RMVar_hsa_circ_374029 26717 RMVar_ID_26717 Human_SNP_ID_666055185 A-to-I Human chr19 - 41334656 41334656 41334656 CTCCTGCCTCAGACTCCCCAGTAGCTGGGATTACAGGTGCCCGCCACCAGGTCCAGCTAATTTTT CTCCTGCCTCAGACTCCCCAGTAGCTGGGATTGCAGGTGCCCGCCACCAGGTCCAGCTAATTTTT T C TGFB1 Ensembl:ENSG00000105329 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1487122341 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_195011,RMVar_hsa_circ_105511,RMVar_hsa_circ_195012,RMVar_hsa_circ_374029 26718 RMVar_ID_26718 Human_SNP_ID_666056093 A-to-I Human chr19 - 41338382 41338382 41338382 TCAAGCAATTCTCCTGCTTCAGCCTCCTGAGTAGTTGGGATTATAGGCACCTGCCACCATGCCCG TCAAGCAATTCTCCTGCTTCAGCCTCCTGAGTCGTTGGGATTATAGGCACCTGCCACCATGCCCG T G TGFB1 Ensembl:ENSG00000105329 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1235020187 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_195011,RMVar_hsa_circ_105511,RMVar_hsa_circ_195012,RMVar_hsa_circ_374029 26719 RMVar_ID_26719 Human_SNP_ID_666056151 A-to-I Human chr19 - 41338588 41338588 41338588 GCAATCCGCCCACCTCAGCCTCCCAAAGTGCTAGGATTACAGGCATGAGCCACTGCTCCCGGCCG GCAATCCGCCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGCTCCCGGCCG T C TGFB1 Ensembl:ENSG00000105329 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1302635052 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_195011,RMVar_hsa_circ_105511,RMVar_hsa_circ_195012,RMVar_hsa_circ_374029 26720 RMVar_ID_26720 Human_SNP_ID_666056200 A-to-I Human chr19 - 41338756 41338756 41338756 CGGCTCACTGCAGCTTCTGCCTCCCGGGTTCAAGTGATTCTCTTGCTTCAGCCTCCCGAGTAGCT CGGCTCACTGCAGCTTCTGCCTCCCGGGTTCAGGTGATTCTCTTGCTTCAGCCTCCCGAGTAGCT T C TGFB1 Ensembl:ENSG00000105329 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs890729495 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_195011,RMVar_hsa_circ_105511,RMVar_hsa_circ_195012,RMVar_hsa_circ_374029 26721 RMVar_ID_26721 Human_SNP_ID_666056356 A-to-I Human chr19 - 41339361 41339361 41339361 TAATCCCAGCACTTTGGGAGGCCAAGGCAGGCAGATCGCTTGAGCTTAGGAGTTCAAGACCAGCT TAATCCCAGCACTTTGGGAGGCCAAGGCAGGCGGATCGCTTGAGCTTAGGAGTTCAAGACCAGCT T C TGFB1 Ensembl:ENSG00000105329 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1232082993 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_195011,RMVar_hsa_circ_105511,RMVar_hsa_circ_195012,RMVar_hsa_circ_374029 26722 RMVar_ID_26722 Human_SNP_ID_666056367 A-to-I Human chr19 - 41339391 41339391 41339391 CTGAAGGCCAGGTGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGCAGA CTGAAGGCCAGGTGCGGTGGCTCATGCCTGTAGTCCCAGCACTTTGGGAGGCCAAGGCAGGCAGA T C TGFB1 Ensembl:ENSG00000105329 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs569381861 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_195011,RMVar_hsa_circ_105511,RMVar_hsa_circ_195012,RMVar_hsa_circ_374029 26723 RMVar_ID_26723 Human_SNP_ID_666056970 A-to-I Human chr19 - 41341351 41341351 41341351 ACGATTCTCCTGTCTCAGCCTCCCGAGTAGCTAGGACTACAGGCACGTGCCACCACGCCCAGCTA ACGATTCTCCTGTCTCAGCCTCCCGAGTAGCTGGGACTACAGGCACGTGCCACCACGCCCAGCTA T C TGFB1 Ensembl:ENSG00000105329 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1270591364 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_195011,RMVar_hsa_circ_105511,RMVar_hsa_circ_195012,RMVar_hsa_circ_374029 26724 RMVar_ID_26724 Human_SNP_ID_666057086 A-to-I Human chr19 - 41341691 41341691 41341691 AACCAGGAGTCTTGTGCCAGGTGCGGTGGCTCACGCCTGTAATCCCAACACTTTGGGAGGCTGAG AACCAGGAGTCTTGTGCCAGGTGCGGTGGCTCGCGCCTGTAATCCCAACACTTTGGGAGGCTGAG T C TGFB1 Ensembl:ENSG00000105329 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs993715728 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_195011,RMVar_hsa_circ_105511,RMVar_hsa_circ_195012,RMVar_hsa_circ_374029 26725 RMVar_ID_26725 Human_SNP_ID_666058526 A-to-I Human chr19 - 41346998 41346998 41346998 ATATAGGCCAGGCGTGGTGGCTCATGCCTGCAATCCCAGCACTTTGGGAGGCCAGGGTGGGTGGA ATATAGGCCAGGCGTGGTGGCTCATGCCTGCACTCCCAGCACTTTGGGAGGCCAGGGTGGGTGGA T G TGFB1 Ensembl:ENSG00000105329 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs527779840 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122732,RMVar_hsa_circ_312712,RMVar_hsa_circ_195011,RMVar_hsa_circ_105511,RMVar_hsa_circ_195012,RMVar_hsa_circ_374029,RMVar_hsa_circ_195015,RMVar_hsa_circ_195017,RMVar_hsa_circ_302286,RMVar_hsa_circ_195019 26726 RMVar_ID_26726 Human_SNP_ID_666058726 A-to-I Human chr19 - 41347789 41347789 41347789 GAGTCTTGCTCTGTCGCCCAGGCTGGAGTACAATGGGGTGATCTCGGCTCACTGCAACCTCCGCC GAGTCTTGCTCTGTCGCCCAGGCTGGAGTACAGTGGGGTGATCTCGGCTCACTGCAACCTCCGCC T C TGFB1 Ensembl:ENSG00000105329 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs867447277 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122732,RMVar_hsa_circ_312712,RMVar_hsa_circ_195011,RMVar_hsa_circ_105511,RMVar_hsa_circ_195012,RMVar_hsa_circ_374029,RMVar_hsa_circ_195015,RMVar_hsa_circ_195017,RMVar_hsa_circ_302286,RMVar_hsa_circ_195019 26727 RMVar_ID_26727 Human_SNP_ID_666064291 A-to-I Human chr19 + 41367613 41367613 41367613 AGATCGTGCCATTGCACTCCATCCTGGGGGACAAGAGTGAGACAAAGTCTCAAAAACAAAACAAA AGATCGTGCCATTGCACTCCATCCTGGGGGACGAGAGTGAGACAAAGTCTCAAAAACAAAACAAA A G TMEM91,AC011462.1 Ensembl:ENSG00000142046,Ensembl:ENSG00000255730 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1253507209 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17567701,Human_RBP_ID_23178591 26728 RMVar_ID_26728 Human_SNP_ID_666064315 A-to-I Human chr19 + 41367695 41367695 41367695 TTGCTCTGTTACCCAGGCTGGAGTGCAGTGGCACAATCACAGCTCACTGCAGCCTCGAACGCCCA TTGCTCTGTTACCCAGGCTGGAGTGCAGTGGCGCAATCACAGCTCACTGCAGCCTCGAACGCCCA A G TMEM91,AC011462.1 Ensembl:ENSG00000142046,Ensembl:ENSG00000255730 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs916693992 Functional Loss SNV dbSNP153 33..33 33 - - - 26729 RMVar_ID_26729 Human_SNP_ID_666064747 A-to-I Human chr19 + 41369448 41369447 41369448 AGGATGCCTTGAGTGCAGGAAGTCCAGGCTGCAGTGAGCTATGATGGCACCCTGCACTCCAGCCT AGGATGCCTTGAGTGCAGGAAGTCCAGGCTGC_GTGAGCTATGATGGCACCCTGCACTCCAGCCT CA C TMEM91,AC011462.1 Ensembl:ENSG00000142046,Ensembl:ENSG00000255730 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1481196950 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_13462281,Human_RBP_ID_17569032,Human_RBP_ID_20395749 26730 RMVar_ID_26730 Human_SNP_ID_666064748 A-to-I Human chr19 + 41369448 41369448 41369448 AGGATGCCTTGAGTGCAGGAAGTCCAGGCTGCAGTGAGCTATGATGGCACCCTGCACTCCAGCCT AGGATGCCTTGAGTGCAGGAAGTCCAGGCTGCCGTGAGCTATGATGGCACCCTGCACTCCAGCCT A C TMEM91,AC011462.1 Ensembl:ENSG00000142046,Ensembl:ENSG00000255730 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1426834217 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13462281,Human_RBP_ID_17569032,Human_RBP_ID_20395749 26731 RMVar_ID_26731 Human_SNP_ID_666065129 A-to-I Human chr19 + 41370713 41370713 41370713 AAGCGTGAGCCACCGTGCCTGGCCACCTATTTATTTTTTTGAGAGGAAGTCTCATTGTGTTGCCT AAGCGTGAGCCACCGTGCCTGGCCACCTATTTGTTTTTTTGAGAGGAAGTCTCATTGTGTTGCCT A G TMEM91,AC011462.1 Ensembl:ENSG00000142046,Ensembl:ENSG00000255730 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1359499005 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13462289 26732 RMVar_ID_26732 Human_SNP_ID_666065130 A-to-I Human chr19 + 41370713 41370713 41370713 AAGCGTGAGCCACCGTGCCTGGCCACCTATTTATTTTTTTGAGAGGAAGTCTCATTGTGTTGCCT AAGCGTGAGCCACCGTGCCTGGCCACCTATTTTTTTTTTTGAGAGGAAGTCTCATTGTGTTGCCT A T TMEM91,AC011462.1 Ensembl:ENSG00000142046,Ensembl:ENSG00000255730 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1359499005 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13462289 26733 RMVar_ID_26733 Human_SNP_ID_666065801 A-to-I Human chr19 + 41372970 41372970 41372970 TGTTTTTGTTTTTGTTTTTGAGACTGGGTTTCACTTTGTTGCCCAGGCTGGACTGCAGTGGCACA TGTTTTTGTTTTTGTTTTTGAGACTGGGTTTCCCTTTGTTGCCCAGGCTGGACTGCAGTGGCACA A C TMEM91,AC011462.1 Ensembl:ENSG00000142046,Ensembl:ENSG00000255730 Protein coding,Protein coding intron,intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1399965038 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569035 26734 RMVar_ID_26734 Human_SNP_ID_666065850 A-to-I Human chr19 + 41373201 41373201 41373201 GGTTTAAGTAATCCTCCCACCTTGGCCTCCCAAAGTGCTGGGATTACAGGCTTGAGCCACCGTAC GGTTTAAGTAATCCTCCCACCTTGGCCTCCCAGAGTGCTGGGATTACAGGCTTGAGCCACCGTAC A G TMEM91,AC011462.1 Ensembl:ENSG00000142046,Ensembl:ENSG00000255730 Protein coding,Protein coding intron,intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1435753872 Functional Loss SNV dbSNP153 33..33 33 - - - 26735 RMVar_ID_26735 Human_SNP_ID_666070788 A-to-I Human chr19 - 41391120 41391120 41391120 CCTCGAGTGATCAGTCCACCTTGGCCTCCCAAAGTGCTGGGGTTACAGGCATGAGCTACTGTGCC CCTCGAGTGATCAGTCCACCTTGGCCTCCCAACGTGCTGGGGTTACAGGCATGAGCTACTGTGCC T G EXOSC5 Ensembl:ENSG00000077348 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903599865 Functional Loss SNV dbSNP153 33..33 33 - - - 26736 RMVar_ID_26736 Human_SNP_ID_666070826 A-to-I Human chr19 - 41391311 41391311 41391311 CCAGGCTGGATGCAGTGGTGCAATGTCAGCTTACTGCAACCTCTACCTCCCGGGCTCAAGCGATT CCAGGCTGGATGCAGTGGTGCAATGTCAGCTTCCTGCAACCTCTACCTCCCGGGCTCAAGCGATT T G EXOSC5 Ensembl:ENSG00000077348 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1009676193 Functional Loss SNV dbSNP153 33..33 33 - - - 26737 RMVar_ID_26737 Human_SNP_ID_666070828 A-to-I Human chr19 - 41391316 41391316 41391316 GTCACCCAGGCTGGATGCAGTGGTGCAATGTCAGCTTACTGCAACCTCTACCTCCCGGGCTCAAG GTCACCCAGGCTGGATGCAGTGGTGCAATGTCGGCTTACTGCAACCTCTACCTCCCGGGCTCAAG T C EXOSC5 Ensembl:ENSG00000077348 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs545921908 Functional Loss SNV dbSNP153 33..33 33 - - - 26738 RMVar_ID_26738 Human_SNP_ID_666070831 A-to-I Human chr19 - 41391321 41391321 41391321 ACTCTGTCACCCAGGCTGGATGCAGTGGTGCAATGTCAGCTTACTGCAACCTCTACCTCCCGGGC ACTCTGTCACCCAGGCTGGATGCAGTGGTGCAGTGTCAGCTTACTGCAACCTCTACCTCCCGGGC T C EXOSC5 Ensembl:ENSG00000077348 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1275009354 Functional Loss SNV dbSNP153 33..33 33 - - - 26739 RMVar_ID_26739 Human_SNP_ID_666070832 A-to-I Human chr19 - 41391322 41391322 41391322 CACTCTGTCACCCAGGCTGGATGCAGTGGTGCAATGTCAGCTTACTGCAACCTCTACCTCCCGGG CACTCTGTCACCCAGGCTGGATGCAGTGGTGCGATGTCAGCTTACTGCAACCTCTACCTCCCGGG T C EXOSC5 Ensembl:ENSG00000077348 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1307578612 Functional Loss SNV dbSNP153 33..33 33 - - - 26740 RMVar_ID_26740 Human_SNP_ID_666070836 A-to-I Human chr19 - 41391353 41391352 41391353 GGTTTTTTTGTTTGTTTTTGAGACAGGCTCTCACTCTGTCACCCAGGCTGGATGCAGTGGTGCAA GGTTTTTTTGTTTGTTTTTGAGACAGGCTCTC_CTCTGTCACCCAGGCTGGATGCAGTGGTGCAA GT G EXOSC5 Ensembl:ENSG00000077348 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1352137357 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_13462545 26741 RMVar_ID_26741 Human_SNP_ID_666077542 A-to-I Human chr19 + 41416798 41416798 41416798 AAAATTAGCCAGGCGTGGTGGTGCACACCTGTAGTCCCAGCTACTCAGGAAGCTGAGTGGGAGGA AAAATTAGCCAGGCGTGGTGGTGCACACCTGTGGTCCCAGCTACTCAGGAAGCTGAGTGGGAGGA A G BCKDHA,AC011462.1 Ensembl:ENSG00000248098,Ensembl:ENSG00000255730 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1336420055 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97634,RMVar_hsa_circ_119890,RMVar_hsa_circ_195027,RMVar_hsa_circ_195025,RMVar_hsa_circ_195026,RMVar_hsa_circ_127513,RMVar_hsa_circ_195029,RMVar_hsa_circ_330724,RMVar_hsa_circ_378800,RMVar_hsa_circ_195030,RMVar_hsa_circ_113602,RMVar_hsa_circ_195032,RMVar_hsa_circ_91877,RMVar_hsa_circ_195031 26742 RMVar_ID_26742 Human_SNP_ID_666083353 A-to-I Human chr19 - 41435177 41435176 41435178 GCCCAGGAGTTCAAGACCAGCCTCGGCAACATAGTGAAACCTCGTCTCTACCAAAATACAAAATT GCCCAGGAGTTCAAGACCAGCCTCGGCAACA__GTGAAACCTCGTCTCTACCAAAATACAAAATT CTA C DMAC2 Ensembl:ENSG00000105341 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1478633276 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_114588,RMVar_hsa_circ_120294,RMVar_hsa_circ_104392,RMVar_hsa_circ_195040,RMVar_hsa_circ_195041,RMVar_hsa_circ_195042 26743 RMVar_ID_26743 Human_SNP_ID_666088723 A-to-I Human chr19 - 41455285 41455285 41455285 CAGGAGTTCAAGACCAGCCTAGGCAACATGATAAAACCCTGTCTCTACTAAAAATACAAAATTAG CAGGAGTTCAAGACCAGCCTAGGCAACATGATGAAACCCTGTCTCTACTAAAAATACAAAATTAG T C PCAT19 Ensembl:ENSG00000267107 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1053238566 Functional Loss SNV dbSNP153 33..33 33 - - - 26744 RMVar_ID_26744 Human_SNP_ID_666194049 A-to-I Human chr19 + 41863157 41863157 41863157 CTCCTGCCCCACCCTCCTAAGTAGCTGGGACTACAGGTGCCTATCAGTCACCATGCCTAGCTAAT CTCCTGCCCCACCCTCCTAAGTAGCTGGGACTGCAGGTGCCTATCAGTCACCATGCCTAGCTAAT A G RPS19 Ensembl:ENSG00000105372 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232524454 Functional Loss SNV dbSNP153 33..33 33 - - - 26745 RMVar_ID_26745 Human_SNP_ID_666194060 A-to-I Human chr19 + 41863203 41863203 41863203 GTCACCATGCCTAGCTAATTTTTTTTATTTGTAGAGATGGAGTCTCACTATGTTGAACTCCCAAG GTCACCATGCCTAGCTAATTTTTTTTATTTGTGGAGATGGAGTCTCACTATGTTGAACTCCCAAG A G RPS19 Ensembl:ENSG00000105372 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs995161524 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9922882,Human_RBP_ID_13462898,Human_RBP_ID_22973475,Human_RBP_ID_26990667 26746 RMVar_ID_26746 Human_SNP_ID_666194327 A-to-I Human chr19 + 41864026 41864026 41864026 CACCACGCCCAGCTAATTTTTCTATTTTTAGTAGAGACGGGTTTTCACCATGTTGGCTGGGATGC CACCACGCCCAGCTAATTTTTCTATTTTTAGTGGAGACGGGTTTTCACCATGTTGGCTGGGATGC A G RPS19 Ensembl:ENSG00000105372 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs782268657 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13462958 26747 RMVar_ID_26747 Human_SNP_ID_666194677 A-to-I Human chr19 + 41865231 41865231 41865231 TCTACTAAAAATAAAAATTAGCCAGGCGTGGTAGCAGGCGCCTGTAGTCCCAGCTACTGGGGAGG TCTACTAAAAATAAAAATTAGCCAGGCGTGGTGGCAGGCGCCTGTAGTCCCAGCTACTGGGGAGG A G RPS19 Ensembl:ENSG00000105372 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1434115585 Functional Loss SNV dbSNP153 33..33 33 - - - 26748 RMVar_ID_26748 Human_SNP_ID_666194826 A-to-I Human chr19 + 41865687 41865687 41865687 CAAGATAACAGAGGCCCGGCGCGGTGGCTCACACCTGTAATCCCAGCACTTTCGGAGGCCGAGGC CAAGATAACAGAGGCCCGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTCGGAGGCCGAGGC A G RPS19 Ensembl:ENSG00000105372 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs977430654 Functional Loss SNV dbSNP153 33..33 33 - - - 26749 RMVar_ID_26749 Human_SNP_ID_666194904 A-to-I Human chr19 + 41865828 41865828 41865828 AAAATTAGCCGGGCGTGGTGGCGGGCGCCTGTAGTCCCAGTTACTGTAGAGGCTGAGGCAGGAGA AAAATTAGCCGGGCGTGGTGGCGGGCGCCTGTCGTCCCAGTTACTGTAGAGGCTGAGGCAGGAGA A C RPS19 Ensembl:ENSG00000105372 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1290903746 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13463031 26750 RMVar_ID_26750 Human_SNP_ID_666195422 A-to-I Human chr19 + 41867327 41867326 41867328 TATATCCTATGTAGATGTTTTACTTTTGAGACAGAGTCTCACTCTGTCACCCAGTCTGGAGTGCA TATATCCTATGTAGATGTTTTACTTTTGAGAC__AGTCTCACTCTGTCACCCAGTCTGGAGTGCA CAG C RPS19 Ensembl:ENSG00000105372 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560370791 Functional Loss DEL dbSNP153 33..34 33 - - - 26751 RMVar_ID_26751 Human_SNP_ID_666195423 A-to-I Human chr19 + 41867327 41867327 41867327 TATATCCTATGTAGATGTTTTACTTTTGAGACAGAGTCTCACTCTGTCACCCAGTCTGGAGTGCA TATATCCTATGTAGATGTTTTACTTTTGAGACGGAGTCTCACTCTGTCACCCAGTCTGGAGTGCA A G RPS19 Ensembl:ENSG00000105372 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1038324512 Functional Loss SNV dbSNP153 33..33 33 - - - 26752 RMVar_ID_26752 Human_SNP_ID_666195473 A-to-I Human chr19 + 41867512 41867512 41867512 TCTTGTAATTTCAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTCCTGACCT TCTTGTAATTTCAGTAGAGATGGGGTTTCACCGTGTTGGCCAGGCTGGTCTCAAACTCCTGACCT A G RPS19 Ensembl:ENSG00000105372 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1157854480 Functional Loss SNV dbSNP153 33..33 33 - - - 26753 RMVar_ID_26753 Human_SNP_ID_666195515 A-to-I Human chr19 + 41867684 41867684 41867684 ATTAATACAGGCCAGACATGGCACATACTTATAGTCCCAGCTACTTAGGAGGCTGAGGCAAGAGG ATTAATACAGGCCAGACATGGCACATACTTATTGTCCCAGCTACTTAGGAGGCTGAGGCAAGAGG A T RPS19 Ensembl:ENSG00000105372 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355238680 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23178680 26754 RMVar_ID_26754 Human_SNP_ID_666195537 A-to-I Human chr19 + 41867762 41867762 41867762 AGGAGTTCGAGGCTGCAGTGAGCTATGATCACACCACAGCACCCCAGCCTGGGTGACAGAATGAG AGGAGTTCGAGGCTGCAGTGAGCTATGATCACCCCACAGCACCCCAGCCTGGGTGACAGAATGAG A C RPS19 Ensembl:ENSG00000105372 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1238387171 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9922920 26755 RMVar_ID_26755 Human_SNP_ID_666196269 A-to-I Human chr19 + 41870028 41870028 41870028 ACTTTGGGATGCCGAGGCAGGCGAATTATCTGAGGTCAGGAGTTCAAGACCATTCTGACCAACAT ACTTTGGGATGCCGAGGCAGGCGAATTATCTGCGGTCAGGAGTTCAAGACCATTCTGACCAACAT A C RPS19 Ensembl:ENSG00000105372 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs879996076 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13463158 26756 RMVar_ID_26756 Human_SNP_ID_666196270 A-to-I Human chr19 + 41870028 41870028 41870028 ACTTTGGGATGCCGAGGCAGGCGAATTATCTGAGGTCAGGAGTTCAAGACCATTCTGACCAACAT ACTTTGGGATGCCGAGGCAGGCGAATTATCTGTGGTCAGGAGTTCAAGACCATTCTGACCAACAT A T RPS19 Ensembl:ENSG00000105372 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs879996076 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13463158 26757 RMVar_ID_26757 Human_SNP_ID_666196621 A-to-I Human chr19 + 41871002 41871002 41871002 CTCCTATCTCAGCTTCCCGAGTAGCTGGGACTACAGGCACACACCACCACACCTGGCTAGTTTTT CTCCTATCTCAGCTTCCCGAGTAGCTGGGACTGCAGGCACACACCACCACACCTGGCTAGTTTTT A G RPS19 Ensembl:ENSG00000105372 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs551981708 Functional Loss SNV dbSNP153 33..33 33 - - - 26758 RMVar_ID_26758 Human_SNP_ID_666196629 A-to-I Human chr19 + 41871035 41871035 41871035 CAGGCACACACCACCACACCTGGCTAGTTTTTATATTTTTAGTAGAGACAGGGTTTCACCATATT CAGGCACACACCACCACACCTGGCTAGTTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATATT A G RPS19 Ensembl:ENSG00000105372 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1465449347 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25420039 26759 RMVar_ID_26759 Human_SNP_ID_666196654 A-to-I Human chr19 + 41871106 41871106 41871106 GCTGGTCTCGAACTCTTGACCTCAGGTGATCCACCTGCCTCGGCCTTCCAGAGTGCTGGGATTAA GCTGGTCTCGAACTCTTGACCTCAGGTGATCCGCCTGCCTCGGCCTTCCAGAGTGCTGGGATTAA A G RPS19 Ensembl:ENSG00000105372 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1455424691 Functional Loss SNV dbSNP153 33..33 33 - - - 26760 RMVar_ID_26760 Human_SNP_ID_666196781 A-to-I Human chr19 + 41871472 41871472 41871472 AGTCTCTTGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCCATCTCAGCTCACTGCAATCTCCGC AGTCTCTTGCTCTGTCGCCCAGGCTGGAGTGCCGTGGCGCCATCTCAGCTCACTGCAATCTCCGC A C RPS19 Ensembl:ENSG00000105372 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1354053108 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2573285,Human_RBP_ID_3572544,Human_RBP_ID_8488653,Human_RBP_ID_8839374 Human_miRNA_ID_301788,Human_miRNA_ID_620183,Human_miRNA_ID_1388722 26761 RMVar_ID_26761 Human_SNP_ID_666196787 A-to-I Human chr19 + 41871486 41871486 41871486 TCGCCCAGGCTGGAGTGCAGTGGCGCCATCTCAGCTCACTGCAATCTCCGCCTTCTGGGTTCAAA TCGCCCAGGCTGGAGTGCAGTGGCGCCATCTCGGCTCACTGCAATCTCCGCCTTCTGGGTTCAAA A G RPS19 Ensembl:ENSG00000105372 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1555842025 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2566429,Human_RBP_ID_3583681,Human_RBP_ID_8488654,Human_RBP_ID_8839374 Human_miRNA_ID_301788,Human_miRNA_ID_867190 26762 RMVar_ID_26762 Human_SNP_ID_666196797 A-to-I Human chr19 + 41871516 41871516 41871516 TCAGCTCACTGCAATCTCCGCCTTCTGGGTTCAAATGATTCTCCTGCCTCAGCCTCCCAAAGTGC TCAGCTCACTGCAATCTCCGCCTTCTGGGTTCGAATGATTCTCCTGCCTCAGCCTCCCAAAGTGC A G RPS19 Ensembl:ENSG00000105372 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1555842035 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2566429,Human_RBP_ID_8488654 26763 RMVar_ID_26763 Human_SNP_ID_666196803 A-to-I Human chr19 + 41871534 41871534 41871534 CGCCTTCTGGGTTCAAATGATTCTCCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAAGTGTGAG CGCCTTCTGGGTTCAAATGATTCTCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAAGTGTGAG A G RPS19 Ensembl:ENSG00000105372 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1389850601 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569041 26764 RMVar_ID_26764 Human_SNP_ID_666196807 A-to-I Human chr19 + 41871556 41871556 41871556 CTCCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAAGTGTGAGCCACTGTGCCTGGTCTGGTTTG CTCCTGCCTCAGCCTCCCAAAGTGCTGGGATTGCAAGTGTGAGCCACTGTGCCTGGTCTGGTTTG A G RPS19 Ensembl:ENSG00000105372 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1450304500 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2566430,Human_RBP_ID_3583682,Human_RBP_ID_17569041,Human_RBP_ID_23178696,Human_RBP_ID_26474032 26765 RMVar_ID_26765 Human_SNP_ID_666196845 A-to-I Human chr19 + 41871704 41871704 41871704 GCTGTTTACCCGGCAGCCAGTCGGGCCTTCCCAGGTCAAACAGTTCCCATCTGGGTTTGGAGGAA GCTGTTTACCCGGCAGCCAGTCGGGCCTTCCCCGGTCAAACAGTTCCCATCTGGGTTTGGAGGAA A C RPS19 Ensembl:ENSG00000105372 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs782787923 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_522608,Human_RBP_ID_17925944 26766 RMVar_ID_26766 Human_SNP_ID_666197158 A-to-I Human chr19 + 41872620 41872620 41872620 CGTAAGGCGTAAGAGTTTAAGAAGTATCGGCCAGGCACAGTGGCTCACACCTGTAATCTCAACAC CGTAAGGCGTAAGAGTTTAAGAAGTATCGGCCGGGCACAGTGGCTCACACCTGTAATCTCAACAC A G RPS19 Ensembl:ENSG00000105372 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1555842258 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13463225,Human_RBP_ID_26474035 26767 RMVar_ID_26767 Human_SNP_ID_666197159 A-to-I Human chr19 + 41872626 41872626 41872626 GCGTAAGAGTTTAAGAAGTATCGGCCAGGCACAGTGGCTCACACCTGTAATCTCAACACTTTGGG GCGTAAGAGTTTAAGAAGTATCGGCCAGGCACGGTGGCTCACACCTGTAATCTCAACACTTTGGG A G RPS19 Ensembl:ENSG00000105372 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs3207020 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13463225,Human_RBP_ID_26474035 26768 RMVar_ID_26768 Human_SNP_ID_666197164 A-to-I Human chr19 + 41872634 41872634 41872634 GTTTAAGAAGTATCGGCCAGGCACAGTGGCTCACACCTGTAATCTCAACACTTTGGGAGGCCGAG GTTTAAGAAGTATCGGCCAGGCACAGTGGCTCGCACCTGTAATCTCAACACTTTGGGAGGCCGAG A G RPS19 Ensembl:ENSG00000105372 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs3170195 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13463225,Human_RBP_ID_26474035 26769 RMVar_ID_26769 Human_SNP_ID_666197165 A-to-I Human chr19 + 41872642 41872642 41872642 AGTATCGGCCAGGCACAGTGGCTCACACCTGTAATCTCAACACTTTGGGAGGCCGAGACGGGCTG AGTATCGGCCAGGCACAGTGGCTCACACCTGTGATCTCAACACTTTGGGAGGCCGAGACGGGCTG A G RPS19 Ensembl:ENSG00000105372 Protein coding 3'UTR GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-Seq:(High) rs3180172 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2566437,Human_RBP_ID_26474035 26770 RMVar_ID_26770 Human_SNP_ID_666197207 A-to-I Human chr19 + 41872774 41872774 41872774 AAAATTAGTTGGGCATGGTGGCGCGCACCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGAAGA AAAATTAGTTGGGCATGGTGGCGCGCACCTGTGATCCCAGCTACTCAGGAGGCTGAGGCAGAAGA A G RPS19 Ensembl:ENSG00000105372 Protein coding 3'UTR GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-Seq:(High) rs1555842289 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2566438,Human_RBP_ID_26468576 26771 RMVar_ID_26771 Human_SNP_ID_666202038 A-to-I Human chr19 + 41890659 41890658 41890659 AAAATTAGCCAGGCACAGTGGTACACACCTGTAATTCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTAGCCAGGCACAGTGGTACACACCTGT_ATTCCAGCTACTCGGGAGGCTGAGGCAGGAGA TA T ARHGEF1 Ensembl:ENSG00000076928 Protein coding exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1240053434 Functional Loss DEL dbSNP153 33..33 33 - - - 26772 RMVar_ID_26772 Human_SNP_ID_666205526 A-to-I Human chr19 + 41900916 41900916 41900916 AGGTTCAAGCGATTGTCCTGCCTCAGCCTCCCAAGTAGCTGGAACTACAGGTGCCCACCACCACT AGGTTCAAGCGATTGTCCTGCCTCAGCCTCCCGAGTAGCTGGAACTACAGGTGCCCACCACCACT A G ARHGEF1 Ensembl:ENSG00000076928 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1270221596 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2012620,Human_Splice_Rec_2012621 26773 RMVar_ID_26773 Human_SNP_ID_666226944 A-to-I Human chr19 - 41975223 41975223 41975223 CATGGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTAGCCGGGCATTGTGGCGGTTGCCTGT CATGGTGAAACCCCGTCTCTACTAAAAATACAGAAAATTAGCCGGGCATTGTGGCGGTTGCCTGT T C AC010616.1,ATP1A3 Ensembl:ENSG00000285505,Ensembl:ENSG00000105409 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1555860692 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_195053,RMVar_hsa_circ_85073 26774 RMVar_ID_26774 Human_SNP_ID_666226950 A-to-I Human chr19 - 41975257 41975257 41975257 CATGAGGTCAGAAGATCGAGACCATCCTGGCTAACATGGTGAAACCCCGTCTCTACTAAAAATAC CATGAGGTCAGAAGATCGAGACCATCCTGGCTGACATGGTGAAACCCCGTCTCTACTAAAAATAC T C AC010616.1,ATP1A3 Ensembl:ENSG00000285505,Ensembl:ENSG00000105409 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1301440106 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_195053,RMVar_hsa_circ_85073 26775 RMVar_ID_26775 Human_SNP_ID_666252083 A-to-I Human chr19 - 42074976 42074976 42074976 GGGAGGCTGAGGCTCGAGATTTGATTGCACCCAGGAGGCCGAGGTTGCAGTGAGCCGAGATCACG GGGAGGCTGAGGCTCGAGATTTGATTGCACCCGGGAGGCCGAGGTTGCAGTGAGCCGAGATCACG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs994720752 Functional Loss SNV dbSNP153 33..33 33 - - - 26776 RMVar_ID_26776 Human_SNP_ID_666258742 A-to-I Human chr19 - 42097398 42097398 42097398 GAGGTCGGGAGTTCGAGACCAGCCTGACCAACATGAAGAAACCCCATCTCTACTAAAAATACAAA GAGGTCGGGAGTTCGAGACCAGCCTGACCAACGTGAAGAAACCCCATCTCTACTAAAAATACAAA T C POU2F2 Ensembl:ENSG00000028277 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1475142884 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37619,RMVar_hsa_circ_41276,RMVar_hsa_circ_319485,RMVar_hsa_circ_195068 26777 RMVar_ID_26777 Human_SNP_ID_666258761 A-to-I Human chr19 - 42097464 42097464 42097464 AGGCAGGGCGCAGTGGTCACCCCTGTAATCCCAGCACTTTGGGAGGCCAAAGCGGGTGGATCACC AGGCAGGGCGCAGTGGTCACCCCTGTAATCCCGGCACTTTGGGAGGCCAAAGCGGGTGGATCACC T C POU2F2 Ensembl:ENSG00000028277 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1402673955 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37619,RMVar_hsa_circ_41276,RMVar_hsa_circ_319485,RMVar_hsa_circ_195068 26778 RMVar_ID_26778 Human_SNP_ID_666258928 A-to-I Human chr19 - 42098301 42098295 42098302 TCAAGCGATTCTCCTACCTCAGCCTCCCAAGTAGCTGGGATTACAAGCATGCGCCACCACACCCA TCAAGCGATTCTCCTACCTCAGCCTCCCAAG_______GATTACAAGCATGCGCCACCACACCCA CCCAGCTA C POU2F2 Ensembl:ENSG00000028277 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs772883812 Functional Loss DEL dbSNP153 32..38 33 - - - RMVar_hsa_circ_37619,RMVar_hsa_circ_41276,RMVar_hsa_circ_319485,RMVar_hsa_circ_195068 26779 RMVar_ID_26779 Human_SNP_ID_666285305 A-to-I Human chr19 - 42210876 42210876 42210876 TAGTAGAGACAGGGTTTCAACCATGTTGGTCAAACTGGTCTCGAACTCCTGATCTCAAGTGATCC TAGTAGAGACAGGGTTTCAACCATGTTGGTCAGACTGGTCTCGAACTCCTGATCTCAAGTGATCC T C DEDD2 Ensembl:ENSG00000160570 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1439648904 Functional Loss SNV dbSNP153 33..33 33 - - - 26780 RMVar_ID_26780 Human_SNP_ID_666285904 A-to-I Human chr19 - 42212871 42212871 42212871 GTTATAGCCATGTTTGGTGGCTCATGCCTGTAATCTTAGTGCTTTGTGTGGCTGAGGCAGGAGGA GTTATAGCCATGTTTGGTGGCTCATGCCTGTATTCTTAGTGCTTTGTGTGGCTGAGGCAGGAGGA T A DEDD2 Ensembl:ENSG00000160570 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1568451572 Functional Loss SNV dbSNP153 33..33 33 - - - 26781 RMVar_ID_26781 Human_SNP_ID_666290482 A-to-I Human chr19 + 42228698 42228698 42228698 ACTGCACCCAGCTAATTTTTGTATTTTAGTAGAGACAGGGTTTTGCCACGTTGACCAGGCTGGTC ACTGCACCCAGCTAATTTTTGTATTTTAGTAGTGACAGGGTTTTGCCACGTTGACCAGGCTGGTC A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs939516274 Functional Loss SNV dbSNP153 33..33 33 - - - 26782 RMVar_ID_26782 Human_SNP_ID_666291149 A-to-I Human chr19 + 42231285 42231285 42231285 AGGAGGCTGAGGCAGGAGAATCACTTGAACCCAGGAGGCAGAAGTTGGAGTGAGCCGGGATTGTG AGGAGGCTGAGGCAGGAGAATCACTTGAACCCGGGAGGCAGAAGTTGGAGTGAGCCGGGATTGTG A G - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1245879224 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8488753 26783 RMVar_ID_26783 Human_SNP_ID_666312055 A-to-I Human chr19 - 42298145 42298145 42298145 TTGCCCAGGCTGGAGTGCGGTGGCATGATCTCAGCTCACTGCAACTTCTGCTTCCAGGGCTCAAG TTGCCCAGGCTGGAGTGCGGTGGCATGATCTCGGCTCACTGCAACTTCTGCTTCCAGGGCTCAAG T C PAFAH1B3 Ensembl:ENSG00000079462 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs998955412 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_195093,RMVar_hsa_circ_119464,RMVar_hsa_circ_195095 26784 RMVar_ID_26784 Human_SNP_ID_666312056 A-to-I Human chr19 - 42298145 42298145 42298145 TTGCCCAGGCTGGAGTGCGGTGGCATGATCTCAGCTCACTGCAACTTCTGCTTCCAGGGCTCAAG TTGCCCAGGCTGGAGTGCGGTGGCATGATCTCCGCTCACTGCAACTTCTGCTTCCAGGGCTCAAG T G PAFAH1B3 Ensembl:ENSG00000079462 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs998955412 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_195093,RMVar_hsa_circ_119464,RMVar_hsa_circ_195095 26785 RMVar_ID_26785 Human_SNP_ID_666312132 A-to-I Human chr19 - 42298482 42298480 42298482 TATCTTTTATTTATTTATTTATTTTGGGACAGAGTCTTGCTCTGTTGCCAGGCCAGAGTGCAGTG TATCTTTTATTTATTTATTTATTTTGGGACAG__TCTTGCTCTGTTGCCAGGCCAGAGTGCAGTG ACT A PAFAH1B3 Ensembl:ENSG00000079462 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1329523689 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_195093,RMVar_hsa_circ_119464,RMVar_hsa_circ_195095 26786 RMVar_ID_26786 Human_SNP_ID_666325585 A-to-I Human chr19 + 42347457 42347457 42347457 TTCCCACCTTAGCCTCCCAAGTAGCTGGGATTACAAACATGCACCACCATGCCTGGCTGTTTTTT TTCCCACCTTAGCCTCCCAAGTAGCTGGGATTGCAAACATGCACCACCATGCCTGGCTGTTTTTT A G MEGF8 Ensembl:ENSG00000105429 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1425236819 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3602,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_335618,RMVar_hsa_circ_92724,RMVar_hsa_circ_195111,RMVar_hsa_circ_116337,RMVar_hsa_circ_195112,RMVar_hsa_circ_195113 26787 RMVar_ID_26787 Human_SNP_ID_666333051 A-to-I Human chr19 + 42371887 42371887 42371887 GGAGGATCACTTGAGCCCGGGGGTTCAAGACCAGCCTGGGCCATATAGTGCAACCCCATCTCTGA GGAGGATCACTTGAGCCCGGGGGTTCAAGACCTGCCTGGGCCATATAGTGCAACCCCATCTCTGA A T MEGF8 Ensembl:ENSG00000105429 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1489852026 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122934,RMVar_hsa_circ_195114 26788 RMVar_ID_26788 Human_SNP_ID_666348816 A-to-I Human chr19 + 42429896 42429896 42429896 AGTCGGCACCTTTAAGAAATCTGGCCGGGCATAGTGGCTTGTGCCTATAATCTCAGCACTTTGGG AGTCGGCACCTTTAAGAAATCTGGCCGGGCATGGTGGCTTGTGCCTATAATCTCAGCACTTTGGG A G LIPE-AS1 Ensembl:ENSG00000213904 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1420454988 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5249181 26789 RMVar_ID_26789 Human_SNP_ID_666348820 A-to-I Human chr19 + 42429910 42429910 42429910 AGAAATCTGGCCGGGCATAGTGGCTTGTGCCTATAATCTCAGCACTTTGGGAGGCCGAGGTGGGC AGAAATCTGGCCGGGCATAGTGGCTTGTGCCTGTAATCTCAGCACTTTGGGAGGCCGAGGTGGGC A G LIPE-AS1 Ensembl:ENSG00000213904 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs932717711 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5249181 26790 RMVar_ID_26790 Human_SNP_ID_666354270 A-to-I Human chr19 + 42453155 42453126 42453156 AAAATTAGCTGGGTGTGGTGGTGTGTGCCTGTAGTCCCAGCTACTTTGGAGGTTGAGGTGTGAGG AAAA______________________________TCCCAGCTACTTTGGAGGTTGAGGTGTGAGG ATTAGCTGGGTGTGGTGGTGTGTGCCTGTAG A LIPE-AS1 Ensembl:ENSG00000213904 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1248721861 Functional Loss DEL dbSNP153 5..34 33 - - - Human_RBP_ID_3589285 26791 RMVar_ID_26791 Human_SNP_ID_666363485 A-to-I Human chr19 + 42492405 42492405 42492405 TGAATAACAGTTCAGTTAAGACAGCCAGGGCCAGGCGTGGTGGCTTATGCCTGTAATCCCAGCAC TGAATAACAGTTCAGTTAAGACAGCCAGGGCCCGGCGTGGTGGCTTATGCCTGTAATCCCAGCAC A C LIPE-AS1 Ensembl:ENSG00000213904 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049676424 Functional Loss SNV dbSNP153 33..33 33 - - - 26792 RMVar_ID_26792 Human_SNP_ID_666363514 A-to-I Human chr19 + 42492529 42492529 42492529 ACATGGTGAAACCCAGTCTCTAATAAAAAAATACAAAATTAGCTGGACATGATGGCGGGTGCCTG ACATGGTGAAACCCAGTCTCTAATAAAAAAATGCAAAATTAGCTGGACATGATGGCGGGTGCCTG A G LIPE-AS1 Ensembl:ENSG00000213904 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1450664101 Functional Loss SNV dbSNP153 33..33 33 - - - 26793 RMVar_ID_26793 Human_SNP_ID_666680632 A-to-I Human chr19 - 43490381 43490381 43490381 AATTTTTGTATTCTTTGTAGACATGGGGTCTCACTATATTGCCCCAGTCTGGTCTCAAATTCCTG AATTTTTGTATTCTTTGTAGACATGGGGTCTCGCTATATTGCCCCAGTCTGGTCTCAAATTCCTG T C PHLDB3 Ensembl:ENSG00000176531 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs954098340 Functional Loss SNV dbSNP153 33..33 33 - - - 26794 RMVar_ID_26794 Human_SNP_ID_666681388 A-to-I Human chr19 - 43493379 43493379 43493379 CTCTTGTTTTAGCCTCCCAAATTGCTGGGATTACAGGCATGAGCCACCGCGCATGGGTCCAATTT CTCTTGTTTTAGCCTCCCAAATTGCTGGGATTGCAGGCATGAGCCACCGCGCATGGGTCCAATTT T C PHLDB3 Ensembl:ENSG00000176531 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs756999166 Functional Loss SNV dbSNP153 33..33 33 - - - 26795 RMVar_ID_26795 Human_SNP_ID_666682327 A-to-I Human chr19 - 43496529 43496529 43496529 CTCCCACCTTGGCCTTTCAAGATGCTGGGATTACAGACATGAGCCACCGTGCCTCGCCACAGCCA CTCCCACCTTGGCCTTTCAAGATGCTGGGATTGCAGACATGAGCCACCGTGCCTCGCCACAGCCA T C PHLDB3 Ensembl:ENSG00000176531 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1284309338 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25420905 RMVar_hsa_circ_361383 26796 RMVar_ID_26796 Human_SNP_ID_666692525 A-to-I Human chr19 - 43532324 43532324 43532324 TGAGCCCAGGATTTCCAAACTAGACGGGGGCTAGGCACGGTGGCTCACGCCTGTAATCCCAGCAC TGAGCCCAGGATTTCCAAACTAGACGGGGGCTGGGCACGGTGGCTCACGCCTGTAATCCCAGCAC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1252993064 Functional Loss SNV dbSNP153 33..33 33 - - - 26797 RMVar_ID_26797 Human_SNP_ID_666703832 A-to-I Human chr19 - 43573681 43573681 43573681 TTTTTTAGAGATGGGGTTTCCACCATGTTGCCAGGCTGGTCTCAAACTCCTGGGCTCAAGCGTTC TTTTTTAGAGATGGGGTTTCCACCATGTTGCCGGGCTGGTCTCAAACTCCTGGGCTCAAGCGTTC T C L34079.1,XRCC1 Ensembl:ENSG00000268361,Ensembl:ENSG00000073050 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1405961099 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87636,RMVar_hsa_circ_195157,RMVar_hsa_circ_195163,RMVar_hsa_circ_346124 26798 RMVar_ID_26798 Human_SNP_ID_666703835 A-to-I Human chr19 - 43573689 43573689 43573689 TTTTGTATTTTTTTAGAGATGGGGTTTCCACCATGTTGCCAGGCTGGTCTCAAACTCCTGGGCTC TTTTGTATTTTTTTAGAGATGGGGTTTCCACCGTGTTGCCAGGCTGGTCTCAAACTCCTGGGCTC T C L34079.1,XRCC1 Ensembl:ENSG00000268361,Ensembl:ENSG00000073050 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1166721407 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_137230,Human_RBP_ID_6767799,Human_RBP_ID_25446691 RMVar_hsa_circ_87636,RMVar_hsa_circ_195157,RMVar_hsa_circ_195163,RMVar_hsa_circ_346124 26799 RMVar_ID_26799 Human_SNP_ID_666703855 A-to-I Human chr19 - 43573775 43573775 43573775 TACCTCCTGGGCTCAAGCGATCCTCCCACCTCAGCCTCCTGAGTAGCTGGGACTGCAGGTGTGCA TACCTCCTGGGCTCAAGCGATCCTCCCACCTCGGCCTCCTGAGTAGCTGGGACTGCAGGTGTGCA T C L34079.1,XRCC1 Ensembl:ENSG00000268361,Ensembl:ENSG00000073050 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1326902888 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_137230 RMVar_hsa_circ_87636,RMVar_hsa_circ_195157,RMVar_hsa_circ_195163,RMVar_hsa_circ_346124 26800 RMVar_ID_26800 Human_SNP_ID_666707630 A-to-I Human chr19 - 43588675 43588675 43588675 TCACTCCATCACCCAGGCTGGAGTGCAGTGGCACGATCTCGCCTCACTGCAACCTCCGCCTCCCA TCACTCCATCACCCAGGCTGGAGTGCAGTGGCGCGATCTCGCCTCACTGCAACCTCCGCCTCCCA T C IRGQ,L34079.1 Ensembl:ENSG00000167378,Ensembl:ENSG00000268361 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1469030502 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13467040 26801 RMVar_ID_26801 Human_SNP_ID_666708241 A-to-I Human chr19 - 43591597 43591597 43591597 GCGATCGACCCGCTCCGGCCTCCCAAAGTGCTAGGATTACAGGCGTGAGCCACCGCCCCTGGCCA GCGATCGACCCGCTCCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCCCCTGGCCA T C IRGQ,L34079.1 Ensembl:ENSG00000167378,Ensembl:ENSG00000268361 Protein coding,Protein coding 3'UTR,intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1297819992 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_241764 26802 RMVar_ID_26802 Human_SNP_ID_666713450 A-to-I Human chr19 + 43609619 43609619 43609619 AAATTTAGCCAAGTGTGGGGTGGTGGGTGCCTATAGTCCCAGCTACTCAGGACTCTGAGGCAGGA AAATTTAGCCAAGTGTGGGGTGGTGGGTGCCTGTAGTCCCAGCTACTCAGGACTCTGAGGCAGGA A G SRRM5 Ensembl:ENSG00000226763 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1159557851 Functional Loss SNV dbSNP153 33..33 33 - - - 26803 RMVar_ID_26803 Human_SNP_ID_666723924 A-to-I Human chr19 - 43649027 43649027 43649027 TGAACCACATTGATGTCTCCTGCTGTACTAAAAGTGGCTGTAACCACCCAGACCTGGATGTCCAG TGAACCACATTGATGTCTCCTGCTGTACTAAAGGTGGCTGTAACCACCCAGACCTGGATGTCCAG T C PLAUR Ensembl:ENSG00000011422 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1408626941 Functional Loss SNV dbSNP153 33..33 33 - - - 26804 RMVar_ID_26804 Human_SNP_ID_666725266 A-to-I Human chr19 - 43654002 43654002 43654002 CCCCTGCCTCAGCCTCCCGAGTGGCTGGGACTACAGGCACCCACCACCATGCCTGGCTAATTTTT CCCCTGCCTCAGCCTCCCGAGTGGCTGGGACTGCAGGCACCCACCACCATGCCTGGCTAATTTTT T C PLAUR Ensembl:ENSG00000011422 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs994769749 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_195171,RMVar_hsa_circ_321581,RMVar_hsa_circ_327308,RMVar_hsa_circ_332226,RMVar_hsa_circ_195169,RMVar_hsa_circ_195170 26805 RMVar_ID_26805 Human_SNP_ID_666725393 A-to-I Human chr19 - 43654502 43654502 43654502 TTGAACTCCTGGGCTTGGCCTCCCAAAGTGTTAGGATTACAGGCATGAGCCACCATGCACCACCA TTGAACTCCTGGGCTTGGCCTCCCAAAGTGTTGGGATTACAGGCATGAGCCACCATGCACCACCA T C PLAUR Ensembl:ENSG00000011422 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1045779191 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_195171,RMVar_hsa_circ_321581,RMVar_hsa_circ_327308,RMVar_hsa_circ_332226,RMVar_hsa_circ_195169,RMVar_hsa_circ_195170 26806 RMVar_ID_26806 Human_SNP_ID_666727260 A-to-I Human chr19 - 43661465 43661465 43661465 TTGAACCCGGGAGGTAGAGGTTACAGTGAGCCAAGATCACACGACTGCACTCCAGCCTGGGCGAC TTGAACCCGGGAGGTAGAGGTTACAGTGAGCCCAGATCACACGACTGCACTCCAGCCTGGGCGAC T G PLAUR Ensembl:ENSG00000011422 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1264306708 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 26807 RMVar_ID_26807 Human_SNP_ID_666727261 A-to-I Human chr19 - 43661469 43661469 43661469 TTGCTTGAACCCGGGAGGTAGAGGTTACAGTGAGCCAAGATCACACGACTGCACTCCAGCCTGGG TTGCTTGAACCCGGGAGGTAGAGGTTACAGTGGGCCAAGATCACACGACTGCACTCCAGCCTGGG T C PLAUR Ensembl:ENSG00000011422 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1225362747 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 26808 RMVar_ID_26808 Human_SNP_ID_666727272 A-to-I Human chr19 - 43661545 43661545 43661545 TAAAAATACAAAAGTTAGCCAGGCGTGGTGGCACATGCCTGTGGTCCCAGCTACTTGGGTGGCTG TAAAAATACAAAAGTTAGCCAGGCGTGGTGGCCCATGCCTGTGGTCCCAGCTACTTGGGTGGCTG T G PLAUR Ensembl:ENSG00000011422 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1427377040 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 26809 RMVar_ID_26809 Human_SNP_ID_666749771 A-to-I Human chr19 - 43747069 43747069 43747069 TCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGTAGGAGAATCACCTAAGCCCAGGAGTTCA TCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGTAGGAGAATCACCTAAGCCCAGGAGTTCA T C SMG9 Ensembl:ENSG00000105771 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1353237831 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118945,RMVar_hsa_circ_98178,RMVar_hsa_circ_195182,RMVar_hsa_circ_195181,RMVar_hsa_circ_195190,RMVar_hsa_circ_83060,RMVar_hsa_circ_195191,RMVar_hsa_circ_292336,RMVar_hsa_circ_308652,RMVar_hsa_circ_195192 26810 RMVar_ID_26810 Human_SNP_ID_666774055 A-to-I Human chr19 + 43843179 43843179 43843179 CCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCTGAGCATGGTGGCAC CCTGGCCAACATGGTGAAACCCCATCTCTACTGAAAATACAAAAATTAGCTGAGCATGGTGGCAC A G ZNF283 Ensembl:ENSG00000167637 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1199575287 Functional Loss SNV dbSNP153 33..33 33 - - - 26811 RMVar_ID_26811 Human_SNP_ID_666774057 A-to-I Human chr19 + 43843188 43843188 43843188 CATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCTGAGCATGGTGGCACGCGCCTGTA CATGGTGAAACCCCATCTCTACTAAAAATACACAAATTAGCTGAGCATGGTGGCACGCGCCTGTA A C ZNF283 Ensembl:ENSG00000167637 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1332810751 Functional Loss SNV dbSNP153 33..33 33 - - - 26812 RMVar_ID_26812 Human_SNP_ID_666774061 A-to-I Human chr19 + 43843194 43843194 43843194 GAAACCCCATCTCTACTAAAAATACAAAAATTAGCTGAGCATGGTGGCACGCGCCTGTAGTCCCA GAAACCCCATCTCTACTAAAAATACAAAAATTTGCTGAGCATGGTGGCACGCGCCTGTAGTCCCA A T ZNF283 Ensembl:ENSG00000167637 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1000165739 Functional Loss SNV dbSNP153 33..33 33 - - - 26813 RMVar_ID_26813 Human_SNP_ID_666775770 A-to-I Human chr19 + 43850539 43850539 43850539 TCGGCTCACTGCAACCTGCACCTCTCGGGTTCAAGTGATTCTCGTGCCTCAGCCTCCCAAGTAGC TCGGCTCACTGCAACCTGCACCTCTCGGGTTCGAGTGATTCTCGTGCCTCAGCCTCCCAAGTAGC A G ZNF283 Ensembl:ENSG00000167637 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1012653958 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_195198 26814 RMVar_ID_26814 Human_SNP_ID_666803677 A-to-I Human chr19 + 43974915 43974915 43974915 GATGTGGTGGTGCATGCCTATAATCCCCAGCTACTTGGGAGGCTGAGGCATGAGAATTGGTTGAA GATGTGGTGGTGCATGCCTATAATCCCCAGCTGCTTGGGAGGCTGAGGCATGAGAATTGGTTGAA A G ZNF155 Ensembl:ENSG00000204920 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1250919816 Functional Loss SNV dbSNP153 33..33 33 - - - 26815 RMVar_ID_26815 Human_SNP_ID_666809217 A-to-I Human chr19 + 43998032 43998032 43998032 GTAAATCATCACTTCAGCTCCTGATTGGTCCCAGGCCAAGCTGAATAGCCCTTAGGAATAATCAC GTAAATCATCACTTCAGCTCCTGATTGGTCCCGGGCCAAGCTGAATAGCCCTTAGGAATAATCAC A G ZNF155 Ensembl:ENSG00000204920 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs377503 Functional Loss SNV dbSNP153 33..33 33 - - - 26816 RMVar_ID_26816 Human_SNP_ID_666822559 A-to-I Human chr19 + 44055334 44055334 44055334 TCTCTTGTCACCTGGCTAATTTTTGTAGTATTAGTGGAGATGGGGTTTCATCATGTTGGCCAGGC TCTCTTGTCACCTGGCTAATTTTTGTAGTATTGGTGGAGATGGGGTTTCATCATGTTGGCCAGGC A G ZNF223,AC067968.1 Ensembl:ENSG00000178386,Ensembl:ENSG00000267022 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968916087 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_340284 26817 RMVar_ID_26817 Human_SNP_ID_666826794 A-to-I Human chr19 + 44073618 44073618 44073618 CAGGCTGGAGTGCAGTGGCACGATCTCGGCTCACTGCTAACTCCGCCTCCCAGGTTCACGCCATT CAGGCTGGAGTGCAGTGGCACGATCTCGGCTCGCTGCTAACTCCGCCTCCCAGGTTCACGCCATT A G ZNF284,AC067968.1 Ensembl:ENSG00000186026,Ensembl:ENSG00000267022 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs543996088 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_340284,RMVar_hsa_circ_195208,RMVar_hsa_circ_113001,RMVar_hsa_circ_302331,RMVar_hsa_circ_50651 26818 RMVar_ID_26818 Human_SNP_ID_666837305 A-to-I Human chr19 + 44115917 44115917 44115917 GGAGACTTGTTCTGTCGCCAAGGCTGGAGTGCAGTGGCCTGATTTTGGCTCATTGCAACCTCCAC GGAGACTTGTTCTGTCGCCAAGGCTGGAGTGCCGTGGCCTGATTTTGGCTCATTGCAACCTCCAC A C ZNF225 Ensembl:ENSG00000256294 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs936055908 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8489555 26819 RMVar_ID_26819 Human_SNP_ID_666840381 A-to-I Human chr19 + 44130437 44130437 44130437 AGGAAAATACAGGGCTGGGCGCAGTGGCTTACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGA AGGAAAATACAGGGCTGGGCGCAGTGGCTTACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGA A G ZNF225 Ensembl:ENSG00000256294 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1334866630 Functional Loss SNV dbSNP153 33..33 33 - - - 26820 RMVar_ID_26820 Human_SNP_ID_666847450 A-to-I Human chr19 + 44159241 44159241 44159241 GCTCTGTCACCGAGGCTGGAGTGCAGTGGCATAATCATGGCTCACTGCAGCCTCGTCCTCCCAGG GCTCTGTCACCGAGGCTGGAGTGCAGTGGCATGATCATGGCTCACTGCAGCCTCGTCCTCCCAGG A G ZNF234 Ensembl:ENSG00000263002 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs139201306 Functional Loss SNV dbSNP153 33..33 33 - - - 26821 RMVar_ID_26821 Human_SNP_ID_666847468 A-to-I Human chr19 + 44159322 44159322 44159322 ATCTCTCCCTCTGAGTAGCTGGGACCACGGGCACGTGCCACCACACCCAGCTAATTTTTGTATGT ATCTCTCCCTCTGAGTAGCTGGGACCACGGGCGCGTGCCACCACACCCAGCTAATTTTTGTATGT A G ZNF234 Ensembl:ENSG00000263002 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1319291786 Functional Loss SNV dbSNP153 33..33 33 - - - 26822 RMVar_ID_26822 Human_SNP_ID_666847478 A-to-I Human chr19 + 44159365 44159365 44159365 CACCCAGCTAATTTTTGTATGTTTGGTAGAGAAAGGGTTTCACCACATTGCCCAGGCTGGTCTTG CACCCAGCTAATTTTTGTATGTTTGGTAGAGAGAGGGTTTCACCACATTGCCCAGGCTGGTCTTG A G ZNF234 Ensembl:ENSG00000263002 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1052943533 Functional Loss SNV dbSNP153 33..33 33 - - - 26823 RMVar_ID_26823 Human_SNP_ID_666847597 A-to-I Human chr19 + 44159885 44159885 44159885 GTGAAACCCCATCTCTACTAAATACAAAAATTAGCTGGGCATGGTGGCAGGCGCCTGTAATCCCA GTGAAACCCCATCTCTACTAAATACAAAAATTCGCTGGGCATGGTGGCAGGCGCCTGTAATCCCA A C ZNF234 Ensembl:ENSG00000263002 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1159049938 Functional Loss SNV dbSNP153 33..33 33 - - - 26824 RMVar_ID_26824 Human_SNP_ID_666847639 A-to-I Human chr19 + 44160014 44160013 44160015 AGACTGCGCCATTGCACTCCAGCTTGGGTGACAGAGCAAGACTCCGTCTCAAAAAAAAAAAAAAA AGACTGCGCCATTGCACTCCAGCTTGGGTGAC__AGCAAGACTCCGTCTCAAAAAAAAAAAAAAA CAG C ZNF234 Ensembl:ENSG00000263002 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs954338714 Functional Loss DEL dbSNP153 33..34 33 - - - 26825 RMVar_ID_26825 Human_SNP_ID_666848085 A-to-I Human chr19 + 44162050 44162050 44162050 AGGCATGGTGGCAGGTGCCTGTAATCCCAGCTACTTGGGAGACTGAGGCAGGAGAATCACTTGAA AGGCATGGTGGCAGGTGCCTGTAATCCCAGCTGCTTGGGAGACTGAGGCAGGAGAATCACTTGAA A G - - Other Unknown GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1417930012 Functional Loss SNV dbSNP153 33..33 33 - - - 26826 RMVar_ID_26826 Human_SNP_ID_666849822 A-to-I Human chr19 + 44169197 44169196 44169198 TGTCCAGCTAATTTTTGTCTTTTAGTAAAGACAGGGTTTCATCTTGTTGGCCAGGCTTGTCTTCA TGTCCAGCTAATTTTTGTCTTTTAGTAAAGAC__GGTTTCATCTTGTTGGCCAGGCTTGTCTTCA CAG C ZNF226 Ensembl:ENSG00000167380 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1568563814 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_43224 26827 RMVar_ID_26827 Human_SNP_ID_666849823 A-to-I Human chr19 + 44169197 44169197 44169197 TGTCCAGCTAATTTTTGTCTTTTAGTAAAGACAGGGTTTCATCTTGTTGGCCAGGCTTGTCTTCA TGTCCAGCTAATTTTTGTCTTTTAGTAAAGACGGGGTTTCATCTTGTTGGCCAGGCTTGTCTTCA A G ZNF226 Ensembl:ENSG00000167380 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1302045657 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43224 26828 RMVar_ID_26828 Human_SNP_ID_666850733 A-to-I Human chr19 + 44172858 44172858 44172858 TTCATTTTCAACTTGTGATTTGGCATTTTCACAGGGCATCCACCCTTCAAACAAGATGTATCACC TTCATTTTCAACTTGTGATTTGGCATTTTCACGGGGCATCCACCCTTCAAACAAGATGTATCACC A G ZNF226 Ensembl:ENSG00000167380 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs954993986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9381092 Human_Splice_Rec_2016681,Human_Splice_Rec_2016701,Human_Splice_Rec_2016729,Human_Splice_Rec_2016747,Human_Splice_Rec_2016759,Human_Splice_Rec_2016769,Human_Splice_Rec_2016779,Human_Splice_Rec_2016819,Human_Splice_Rec_2016831,Human_Splice_Rec_2016841,Human_Splice_Rec_2016851 RMVar_hsa_circ_20511,RMVar_hsa_circ_43224,RMVar_hsa_circ_195213,RMVar_hsa_circ_327006 26829 RMVar_ID_26829 Human_SNP_ID_666864322 A-to-I Human chr19 + 44228120 44228120 44228120 GGGCATGGTAGTAGACGCCTGTAATCCCACCTACTTGGGAGGCTAAGGCAGGAGAATCTCTTGAA GGGCATGGTAGTAGACGCCTGTAATCCCACCTTCTTGGGAGGCTAAGGCAGGAGAATCTCTTGAA A T ZNF227 Ensembl:ENSG00000131115 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs984057063 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_297172,RMVar_hsa_circ_34837,RMVar_hsa_circ_318518 26830 RMVar_ID_26830 Human_SNP_ID_666864323 A-to-I Human chr19 + 44228137 44228137 44228137 CCTGTAATCCCACCTACTTGGGAGGCTAAGGCAGGAGAATCTCTTGAACCCGGGAGGCGGAGGTT CCTGTAATCCCACCTACTTGGGAGGCTAAGGCGGGAGAATCTCTTGAACCCGGGAGGCGGAGGTT A G ZNF227 Ensembl:ENSG00000131115 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1433314990 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_297172,RMVar_hsa_circ_34837,RMVar_hsa_circ_318518 26831 RMVar_ID_26831 Human_SNP_ID_666864412 A-to-I Human chr19 - 44228477 44228477 44228477 GATCGAGCAGTCGCAGTTCCTCCCTGGAGAAGACCACAGCCACATCCTTGAATGTCACAGCCTCC GATCGAGCAGTCGCAGTTCCTCCCTGGAGAAGCCCACAGCCACATCCTTGAATGTCACAGCCTCC T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs745662964 Functional Loss SNV dbSNP153 33..33 33 - - - 26832 RMVar_ID_26832 Human_SNP_ID_666867364 A-to-I Human chr19 + 44238495 44238495 44238495 TTTTGTAGAGATGGGCTCTCGCTATGTTGTCTAAGCTGGTATCGAACTCTTGGGCTTAAGTGATC TTTTGTAGAGATGGGCTCTCGCTATGTTGTCTTAGCTGGTATCGAACTCTTGGGCTTAAGTGATC A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1019662055 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8097873 26833 RMVar_ID_26833 Human_SNP_ID_666872899 A-to-I Human chr19 - 44261320 44261320 44261320 GGGCTCAAGCGATCCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACCACAGGTGTGTGGCTAATTT GGGCTCAAGCGATCCTCCTGCCTCAGCCTCCCTAGTAGCTGGGACCACAGGTGTGTGGCTAATTT T A ZNF235 Ensembl:ENSG00000159917 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs772786134 Functional Loss SNV dbSNP153 33..33 33 - - - 26834 RMVar_ID_26834 Human_SNP_ID_666872902 A-to-I Human chr19 - 44261328 44261328 44261328 TGCCTCCTGGGCTCAAGCGATCCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACCACAGGTGTGTG TGCCTCCTGGGCTCAAGCGATCCTCCTGCCTCGGCCTCCCAAGTAGCTGGGACCACAGGTGTGTG T C ZNF235 Ensembl:ENSG00000159917 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264990087 Functional Loss SNV dbSNP153 33..33 33 - - - 26835 RMVar_ID_26835 Human_SNP_ID_666874565 A-to-I Human chr19 + 44267642 44267642 44267642 GAGCTCAAGCAATCCTCCCACTTCAGCCTCCCAAAGTGTTAGGATTACAGGCATGAGCCACTGTG GAGCTCAAGCAATCCTCCCACTTCAGCCTCCCGAAGTGTTAGGATTACAGGCATGAGCCACTGTG A G ZNF233 Ensembl:ENSG00000159915 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs942966204 Functional Loss SNV dbSNP153 33..33 33 - - - 26836 RMVar_ID_26836 Human_SNP_ID_666876328 A-to-I Human chr19 - 44274334 44274334 44274334 CACACATCACATTTGTAGGGATTCTCTCCAGTATGGACTTGCTGATGGTCTTGGAGATGCGAACT CACACATCACATTTGTAGGGATTCTCTCCAGTGTGGACTTGCTGATGGTCTTGGAGATGCGAACT T C ZNF235 Ensembl:ENSG00000159917 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs769781632 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4535490 26837 RMVar_ID_26837 Human_SNP_ID_666880120 A-to-I Human chr19 - 44289091 44289091 44289091 ATGCTGGCAAATCAAGAGACACATTGCGAGCAAATTAGCCAGAAGTCAAGACTCCATGATAAATA ATGCTGGCAAATCAAGAGACACATTGCGAGCATATTAGCCAGAAGTCAAGACTCCATGATAAATA T A ZNF235 Ensembl:ENSG00000159917 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs774059403 Functional Loss SNV dbSNP153 33..33 33 - - - 26838 RMVar_ID_26838 Human_SNP_ID_666882004 A-to-I Human chr19 - 44298032 44298032 44298032 TCACTGCAGTCTCCACCTCCTGTGCTCAAGCAATCCTCCCACCTCAGCCTTCTGAGTAGCTGGAA TCACTGCAGTCTCCACCTCCTGTGCTCAAGCAGTCCTCCCACCTCAGCCTTCTGAGTAGCTGGAA T C ZNF235 Ensembl:ENSG00000159917 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1026335778 Functional Loss SNV dbSNP153 33..33 33 - - - 26839 RMVar_ID_26839 Human_SNP_ID_666882008 A-to-I Human chr19 - 44298037 44298037 44298037 TCGGCTCACTGCAGTCTCCACCTCCTGTGCTCAAGCAATCCTCCCACCTCAGCCTTCTGAGTAGC TCGGCTCACTGCAGTCTCCACCTCCTGTGCTCGAGCAATCCTCCCACCTCAGCCTTCTGAGTAGC T C ZNF235 Ensembl:ENSG00000159917 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs562681440 Functional Loss SNV dbSNP153 33..33 33 - - - 26840 RMVar_ID_26840 Human_SNP_ID_666928480 A-to-I Human chr19 - 44476851 44476849 44476851 GCTCTCAGCTTGTTGCACATCAAAGAACTCACACTGGAGAGAAACCGTATGAATGTAGTGAATGT GCTCTCAGCTTGTTGCACATCAAAGAACTCAC__TGGAGAGAAACCGTATGAATGTAGTGAATGT AGT A ZNF180 Ensembl:ENSG00000167384 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs779989307 Functional Loss DEL dbSNP153 33..34 33 - - - Human_miRNA_ID_505408,Human_miRNA_ID_512616,Human_miRNA_ID_1541195,Human_miRNA_ID_1594711 26841 RMVar_ID_26841 Human_SNP_ID_666933634 A-to-I Human chr19 - 44496497 44496497 44496497 GGCTTATATTTTTTGTGTGTGTGTATTTTAAAAATTTTTTGTAGAAACGATATCTCACTATGTTT GGCTTATATTTTTTGTGTGTGTGTATTTTAAACATTTTTTGTAGAAACGATATCTCACTATGTTT T G ZNF180 Ensembl:ENSG00000167384 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1211849506 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1889980,Human_RBP_ID_3573642,Human_RBP_ID_13471909 26842 RMVar_ID_26842 Human_SNP_ID_666933636 A-to-I Human chr19 - 44496500 44496500 44496500 CCTGGCTTATATTTTTTGTGTGTGTGTATTTTAAAAATTTTTTGTAGAAACGATATCTCACTATG CCTGGCTTATATTTTTTGTGTGTGTGTATTTTTAAAATTTTTTGTAGAAACGATATCTCACTATG T A ZNF180 Ensembl:ENSG00000167384 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1035222881 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1889980,Human_RBP_ID_3573643,Human_RBP_ID_13471909 26843 RMVar_ID_26843 Human_SNP_ID_666974817 A-to-I Human chr19 + 44652629 44652629 44652629 TGGTCTCAAACTCCTGACCTCGTGATCCACCCACCTTGGCCTCCCAAATTGCTGGGATTACAGAC TGGTCTCAAACTCCTGACCTCGTGATCCACCCGCCTTGGCCTCCCAAATTGCTGGGATTACAGAC A G PVR Ensembl:ENSG00000073008 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs908698118 Functional Loss SNV dbSNP153 33..33 33 - - - 26844 RMVar_ID_26844 Human_SNP_ID_666975737 A-to-I Human chr19 + 44655901 44655901 44655901 TTTTTTTTTTTTTTTTTTTGAGGCAGGGCCTCACTCTGTTGCTCAGGCTGTAGTGCCGTGGCACA TTTTTTTTTTTTTTTTTTTGAGGCAGGGCCTCGCTCTGTTGCTCAGGCTGTAGTGCCGTGGCACA A G PVR Ensembl:ENSG00000073008 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1450063013 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13472207 RMVar_hsa_circ_3719 26845 RMVar_ID_26845 Human_SNP_ID_666977382 A-to-I Human chr19 + 44662389 44662379 44662389 GTCATCCTCCCACCTCAGCCTCCTGAGTAGCTATGACTACAGGTATGTGCCACCACGTCTGGCTA GTCATCCTCCCACCTCAGCCTCC__________TGACTACAGGTATGTGCCACCACGTCTGGCTA CTGAGTAGCTA C PVR,CEACAM19 Ensembl:ENSG00000073008,Ensembl:ENSG00000186567 Protein coding,Protein coding 3'UTR,5'UTR GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1314240247 Functional Loss DEL dbSNP153 24..33 33 - - - Human_RBP_ID_1294952 Human_Splice_Rec_2017489,Human_Splice_Rec_2017495,Human_Splice_Rec_2017503,Human_Splice_Rec_2017511,Human_Splice_Rec_2017515 Human_miRNA_ID_1136158,Human_miRNA_ID_1136159,Human_miRNA_ID_1138672,Human_miRNA_ID_1138673 26846 RMVar_ID_26846 Human_SNP_ID_666977386 A-to-I Human chr19 + 44662395 44662395 44662395 CTCCCACCTCAGCCTCCTGAGTAGCTATGACTACAGGTATGTGCCACCACGTCTGGCTAATCTTT CTCCCACCTCAGCCTCCTGAGTAGCTATGACTGCAGGTATGTGCCACCACGTCTGGCTAATCTTT A G PVR,CEACAM19 Ensembl:ENSG00000073008,Ensembl:ENSG00000186567 Protein coding,Protein coding 3'UTR,5'UTR GSE100210;GSE107867;GSE123020:GSM3490829,GSM3490830,GSM3490831 HepG2 cell line;ASD brains,frontal_cortex;esophageal squamous carcinoma cells,EC109 cell line - 29129909,30559470,32596459 RNA-Seq:(High) rs966360958 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2017489,Human_Splice_Rec_2017495,Human_Splice_Rec_2017503,Human_Splice_Rec_2017511,Human_Splice_Rec_2017515 26847 RMVar_ID_26847 Human_SNP_ID_666977685 A-to-I Human chr19 + 44663810 44663810 44663810 GACGGTGTCTCCTGTCACCCAGGCTGGAGTGCAATGGCACGATCATAGCTCATTGCAGCCTCTAA GACGGTGTCTCCTGTCACCCAGGCTGGAGTGCCATGGCACGATCATAGCTCATTGCAGCCTCTAA A C PVR,CEACAM19 Ensembl:ENSG00000073008,Ensembl:ENSG00000186567 Protein coding,Protein coding 3'UTR,intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1295480632 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6772838 26848 RMVar_ID_26848 Human_SNP_ID_666977690 A-to-I Human chr19 + 44663822 44663822 44663822 TGTCACCCAGGCTGGAGTGCAATGGCACGATCATAGCTCATTGCAGCCTCTAACTCCGGGGCTCA TGTCACCCAGGCTGGAGTGCAATGGCACGATCGTAGCTCATTGCAGCCTCTAACTCCGGGGCTCA A G PVR,CEACAM19 Ensembl:ENSG00000073008,Ensembl:ENSG00000186567 Protein coding,Protein coding 3'UTR,intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1422128487 Functional Loss SNV dbSNP153 33..33 33 - - - 26849 RMVar_ID_26849 Human_SNP_ID_666977702 A-to-I Human chr19 + 44663880 44663880 44663880 GGGCTCAAGCAATCCTCCCACCTCAGCCTACCAAGTAGCTGTGACCACAGCTGCCCCTCACCATG GGGCTCAAGCAATCCTCCCACCTCAGCCTACCGAGTAGCTGTGACCACAGCTGCCCCTCACCATG A G PVR,CEACAM19 Ensembl:ENSG00000073008,Ensembl:ENSG00000186567 Protein coding,Protein coding 3'UTR,intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs557010676 Functional Loss SNV dbSNP153 33..33 33 - - - 26850 RMVar_ID_26850 Human_SNP_ID_666977854 A-to-I Human chr19 + 44664481 44664481 44664481 GTGCTCCTCCTGCCTTGGCCTCCCAAAGCGCTAGGATTACAGATGTGAGCCACCGCGCCCACCCT GTGCTCCTCCTGCCTTGGCCTCCCAAAGCGCTCGGATTACAGATGTGAGCCACCGCGCCCACCCT A C AC243964.4,PVR,CEACAM19 Ensembl:ENSG00000279095,Ensembl:ENSG00000073008,Ensembl:ENSG00000186567 Other,Protein coding,Protein coding exon,3'UTR,intron GSE47997;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,29129909,31158229,31158229,32596459,32596459 RNA-Seq:(High) rs953239862 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_240917 26851 RMVar_ID_26851 Human_SNP_ID_666978088 A-to-I Human chr19 + 44665383 44665383 44665383 TACAAAAAATTACGGGCTGGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGCA TACAAAAAATTACGGGCTGGGCGCAGTGGCTCCCGCCTGTAATCCCAGCACTTTGGGAGGCTGCA A C AC243964.4,PVR,CEACAM19 Ensembl:ENSG00000279095,Ensembl:ENSG00000073008,Ensembl:ENSG00000186567 Other,Protein coding,Protein coding exon,3'UTR,intron GSE47997;GSE126723:GSM3611827,GSM3611828,GSM3611829 K562 cells&HepG2 cells;Bronchiolar epithelium,BEP2D cell line - 23474544,31158229 RNA-Seq:(High) rs993319559 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_3146646,Human_miRNA_ID_3156817,Human_miRNA_ID_3161616,Human_miRNA_ID_3161851,Human_miRNA_ID_3168168,Human_miRNA_ID_3168387,Human_miRNA_ID_3168827,Human_miRNA_ID_3180440,Human_miRNA_ID_3180658,Human_miRNA_ID_3195486,Human_miRNA_ID_3198284,Human_miRNA_ID_3199158,Human_miRNA_ID_3215948 26852 RMVar_ID_26852 Human_SNP_ID_666978137 A-to-I Human chr19 + 44665554 44665554 44665554 TACTCAGAAGGCTGAGGTGGGAGAATCCCTTGAACCCGGGAAGTGGAGGCTGGAGTAAACCATGA TACTCAGAAGGCTGAGGTGGGAGAATCCCTTGTACCCGGGAAGTGGAGGCTGGAGTAAACCATGA A T AC243964.4,PVR,CEACAM19 Ensembl:ENSG00000279095,Ensembl:ENSG00000073008,Ensembl:ENSG00000186567 Other,Protein coding,Protein coding exon,3'UTR,intron GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,29796672,31158229,31158229 RNA-Seq:(High) rs997171949 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5261927 26853 RMVar_ID_26853 Human_SNP_ID_666978140 A-to-I Human chr19 + 44665578 44665578 44665578 ATCCCTTGAACCCGGGAAGTGGAGGCTGGAGTAAACCATGATCGAGTTACTGCACTCCAGCCTGG ATCCCTTGAACCCGGGAAGTGGAGGCTGGAGTGAACCATGATCGAGTTACTGCACTCCAGCCTGG A G AC243964.4,PVR,CEACAM19 Ensembl:ENSG00000279095,Ensembl:ENSG00000073008,Ensembl:ENSG00000186567 Other,Protein coding,Protein coding exon,3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs868847709 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23309727,Human_RBP_ID_25447124 26854 RMVar_ID_26854 Human_SNP_ID_666978141 A-to-I Human chr19 + 44665578 44665578 44665578 ATCCCTTGAACCCGGGAAGTGGAGGCTGGAGTAAACCATGATCGAGTTACTGCACTCCAGCCTGG ATCCCTTGAACCCGGGAAGTGGAGGCTGGAGTTAACCATGATCGAGTTACTGCACTCCAGCCTGG A T AC243964.4,PVR,CEACAM19 Ensembl:ENSG00000279095,Ensembl:ENSG00000073008,Ensembl:ENSG00000186567 Other,Protein coding,Protein coding exon,3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs868847709 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23309727,Human_RBP_ID_25447124 26855 RMVar_ID_26855 Human_SNP_ID_666978142 A-to-I Human chr19 + 44665583 44665583 44665583 TTGAACCCGGGAAGTGGAGGCTGGAGTAAACCATGATCGAGTTACTGCACTCCAGCCTGGGTGAC TTGAACCCGGGAAGTGGAGGCTGGAGTAAACCGTGATCGAGTTACTGCACTCCAGCCTGGGTGAC A G AC243964.4,PVR,CEACAM19 Ensembl:ENSG00000279095,Ensembl:ENSG00000073008,Ensembl:ENSG00000186567 Other,Protein coding,Protein coding exon,3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1226881953 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23309727,Human_RBP_ID_25447124 26856 RMVar_ID_26856 Human_SNP_ID_666978398 A-to-I Human chr19 + 44666547 44666547 44666547 CAAAAATAAGCCGGGCGTGGTGGCGTGCGCCTATAGTCCCAGCTACTCGGGAGGCTGAGGCAAGA CAAAAATAAGCCGGGCGTGGTGGCGTGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAAGA A G CEACAM19 Ensembl:ENSG00000186567 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs543178404 Functional Loss SNV dbSNP153 33..33 33 - - - 26857 RMVar_ID_26857 Human_SNP_ID_666980153 A-to-I Human chr19 + 44670417 44670417 44670417 CACTCTGGGGCTGGGTGCAGTGGCTCATGCCTATACTCCTAGTACTTTGGGAGGCCGAGGCAGGA CACTCTGGGGCTGGGTGCAGTGGCTCATGCCTGTACTCCTAGTACTTTGGGAGGCCGAGGCAGGA A G CEACAM19 Ensembl:ENSG00000186567 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1296988342 Functional Loss SNV dbSNP153 33..33 33 - - - 26858 RMVar_ID_26858 Human_SNP_ID_667000536 A-to-I Human chr19 + 44744685 44744685 44744685 CTCAATTCAAAACAAAGTAGGACAAGGAAGCCAGATGCGGTGGCTCACGCCTGTAATCCCAGCAC CTCAATTCAAAACAAAGTAGGACAAGGAAGCCTGATGCGGTGGCTCACGCCTGTAATCCCAGCAC A T lnc-BCL3-1,lnc-BCL3-1:2 RNACentral:URS00008B5DE3,RNACentral:URS00008BAA26 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1010101956 Functional Loss SNV dbSNP153 33..33 33 - - - 26859 RMVar_ID_26859 Human_SNP_ID_667002098 A-to-I Human chr19 + 44750398 44750398 44750398 TCGGCTCACTGCAACCTCCGCCTCCCAAGTTCAGGGGATTCTTGTGCCTCAGCCTCCCGAGTAGC TCGGCTCACTGCAACCTCCGCCTCCCAAGTTCTGGGGATTCTTGTGCCTCAGCCTCCCGAGTAGC A T BCL3 Ensembl:ENSG00000069399 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1429092977 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84901,RMVar_hsa_circ_195226 26860 RMVar_ID_26860 Human_SNP_ID_667002637 A-to-I Human chr19 + 44752416 44752416 44752416 TGTAGAAACACAGCAGTCTTGCTATGTTGCCCAGACTGGTCTCAAACTCCTGGGCTTAAGTGATC TGTAGAAACACAGCAGTCTTGCTATGTTGCCCTGACTGGTCTCAAACTCCTGGGCTTAAGTGATC A T BCL3 Ensembl:ENSG00000069399 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1307725393 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84901,RMVar_hsa_circ_126736,RMVar_hsa_circ_195226,RMVar_hsa_circ_195228,RMVar_hsa_circ_106781,RMVar_hsa_circ_195227 26861 RMVar_ID_26861 Human_SNP_ID_667032792 A-to-I Human chr19 + 44859688 44859688 44859688 TCTACTAAAAATTCAAAAATCAGCCGGACCGTAGTGGCTCGCACCTGTAATCCCAGCTACTCAGG TCTACTAAAAATTCAAAAATCAGCCGGACCGTGGTGGCTCGCACCTGTAATCCCAGCTACTCAGG A G NECTIN2 Ensembl:ENSG00000130202 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1241435529 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122951,RMVar_hsa_circ_195240 26862 RMVar_ID_26862 Human_SNP_ID_667032933 A-to-I Human chr19 + 44860296 44860296 44860296 CCCGTAATCCGAACACTTTGGGAGGCCGAGGCAGGTGGATCGCTTGAGCTCAGGAGCCTAAGCAA CCCGTAATCCGAACACTTTGGGAGGCCGAGGCGGGTGGATCGCTTGAGCTCAGGAGCCTAAGCAA A G NECTIN2 Ensembl:ENSG00000130202 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1341516055 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122951,RMVar_hsa_circ_195240 26863 RMVar_ID_26863 Human_SNP_ID_667033040 A-to-I Human chr19 + 44860754 44860754 44860754 CGCCTCCTGGGTTCAAGTGAACACGTCCGGCTAATTTTTATATTTTTAGTAGAGACAGGGTATTT CGCCTCCTGGGTTCAAGTGAACACGTCCGGCTCATTTTTATATTTTTAGTAGAGACAGGGTATTT A C NECTIN2 Ensembl:ENSG00000130202 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1431520287 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122951,RMVar_hsa_circ_195240 26864 RMVar_ID_26864 Human_SNP_ID_667033044 A-to-I Human chr19 + 44860778 44860777 44860779 GTCCGGCTAATTTTTATATTTTTAGTAGAGACAGGGTATTTCACCGTGTTGGCCAGGCTGGTCTC GTCCGGCTAATTTTTATATTTTTAGTAGAGAC__GGTATTTCACCGTGTTGGCCAGGCTGGTCTC CAG C NECTIN2 Ensembl:ENSG00000130202 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1308613863 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_122951,RMVar_hsa_circ_195240 26865 RMVar_ID_26865 Human_SNP_ID_667039557 A-to-I Human chr19 + 44884223 44884223 44884223 TCACTCTGTCCCTCAGGCTAGAGTTCAGTGGTATAATCTGAGCTCACTGCAACCTTCGCCTCCTG TCACTCTGTCCCTCAGGCTAGAGTTCAGTGGTGTAATCTGAGCTCACTGCAACCTTCGCCTCCTG A G NECTIN2 Ensembl:ENSG00000130202 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs907562036 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122951,RMVar_hsa_circ_195240,RMVar_hsa_circ_118252,RMVar_hsa_circ_195243,RMVar_hsa_circ_326410,RMVar_hsa_circ_118992,RMVar_hsa_circ_195248 26866 RMVar_ID_26866 Human_SNP_ID_667043039 A-to-I Human chr19 + 44895747 44895747 44895747 TTTTGTATTTTTAGTAGAGACAGGTTTTCGCCATGTCGGCCAGGCTGATCTCGAACTTCTTACCT TTTTGTATTTTTAGTAGAGACAGGTTTTCGCCCTGTCGGCCAGGCTGATCTCGAACTTCTTACCT A C TOMM40 Ensembl:ENSG00000130204 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs911714209 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13472613 RMVar_hsa_circ_53813 26867 RMVar_ID_26867 Human_SNP_ID_667043040 A-to-I Human chr19 + 44895747 44895747 44895747 TTTTGTATTTTTAGTAGAGACAGGTTTTCGCCATGTCGGCCAGGCTGATCTCGAACTTCTTACCT TTTTGTATTTTTAGTAGAGACAGGTTTTCGCCGTGTCGGCCAGGCTGATCTCGAACTTCTTACCT A G TOMM40 Ensembl:ENSG00000130204 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs911714209 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13472613 RMVar_hsa_circ_53813 26868 RMVar_ID_26868 Human_SNP_ID_667043365 A-to-I Human chr19 + 44896873 44896873 44896873 GATCGGGAGTTCAAGATCAGCCTGGGCAACATAGCAATACCCTGTCTCTACAAAAAAAATTAGAA GATCGGGAGTTCAAGATCAGCCTGGGCAACATCGCAATACCCTGTCTCTACAAAAAAAATTAGAA A C TOMM40 Ensembl:ENSG00000130204 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs745666164 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_53813 26869 RMVar_ID_26869 Human_SNP_ID_667043592 A-to-I Human chr19 + 44897706 44897706 44897706 TGAGGCAGGAGAGTCACTTGAACCCGGGAGGCAGAGGTTGCAGTGAGCCGAGATGACGCCTTTGC TGAGGCAGGAGAGTCACTTGAACCCGGGAGGCGGAGGTTGCAGTGAGCCGAGATGACGCCTTTGC A G TOMM40 Ensembl:ENSG00000130204 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1358435385 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_53813 26870 RMVar_ID_26870 Human_SNP_ID_667044795 A-to-I Human chr19 + 44901434 44901434 44901434 TGTGCTGCCACCCTGTGGGCCTCCACATTACCAGGGAACACTTGTTAAAAGGTAGGTGGGGCCGG TGTGCTGCCACCCTGTGGGCCTCCACATTACCGGGGAACACTTGTTAAAAGGTAGGTGGGGCCGG A G TOMM40 Ensembl:ENSG00000130204 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs405697 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26759711 Human_Splice_Rec_2017915 GWAS_ID_2763,GWAS_ID_2764,GWAS_ID_2765,GWAS_ID_2766,GWAS_ID_2767,GWAS_ID_2768,GWAS_ID_2769,GWAS_ID_2770 26871 RMVar_ID_26871 Human_SNP_ID_667044796 A-to-I Human chr19 + 44901434 44901434 44901434 TGTGCTGCCACCCTGTGGGCCTCCACATTACCAGGGAACACTTGTTAAAAGGTAGGTGGGGCCGG TGTGCTGCCACCCTGTGGGCCTCCACATTACCTGGGAACACTTGTTAAAAGGTAGGTGGGGCCGG A T TOMM40 Ensembl:ENSG00000130204 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs405697 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26759711 Human_Splice_Rec_2017915 GWAS_ID_2763,GWAS_ID_2764,GWAS_ID_2765,GWAS_ID_2766,GWAS_ID_2767,GWAS_ID_2768,GWAS_ID_2769,GWAS_ID_2770 26872 RMVar_ID_26872 Human_SNP_ID_667044850 A-to-I Human chr19 + 44901617 44901617 44901617 ACAAAATTAGCCGGGTGTGGTTGCGGGTGCCTATAGTCCCAACTACTGAGGCTGAGGCGGGAAAA ACAAAATTAGCCGGGTGTGGTTGCGGGTGCCTGTAGTCCCAACTACTGAGGCTGAGGCGGGAAAA A G TOMM40 Ensembl:ENSG00000130204 Protein coding intron GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs1402055048 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22974377 26873 RMVar_ID_26873 Human_SNP_ID_667045074 A-to-I Human chr19 + 44902404 44902404 44902404 TTTTTGATAGTTTTGGGAGACATGGGGGTTTCACCATGTTGCCCAGGCTGGTCTCGAACTCCTGG TTTTTGATAGTTTTGGGAGACATGGGGGTTTCGCCATGTTGCCCAGGCTGGTCTCGAACTCCTGG A G TOMM40 Ensembl:ENSG00000130204 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1295058625 Functional Loss SNV dbSNP153 33..33 33 - - - 26874 RMVar_ID_26874 Human_SNP_ID_667045085 A-to-I Human chr19 + 44902470 44902470 44902470 CTCAAGCCTTGGCCTCCCAAAGTGCTGGGATTATAGGTGTGAGCCACCACACCCAGCCAGGGTAG CTCAAGCCTTGGCCTCCCAAAGTGCTGGGATTTTAGGTGTGAGCCACCACACCCAGCCAGGGTAG A T TOMM40 Ensembl:ENSG00000130204 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs528866966 Functional Loss SNV dbSNP153 33..33 33 - - - 26875 RMVar_ID_26875 Human_SNP_ID_667054246 A-to-I Human chr19 + 44931283 44931283 44931283 CGGGCGGATCACAAGGTCAGGAGATTGAGCCCATCCTGGCTAACACGGTGAAACCCCGTCTCTAC CGGGCGGATCACAAGGTCAGGAGATTGAGCCCGTCCTGGCTAACACGGTGAAACCCCGTCTCTAC A G APOC1P1 Ensembl:ENSG00000214855 Pseudogene exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1348651129 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9929786,Human_RBP_ID_17387658 26876 RMVar_ID_26876 Human_SNP_ID_667054269 A-to-I Human chr19 + 44931350 44931350 44931350 AAAATACAAAAAAAATAGCCAAGCGTGGTGGCAGGCGCCTGTAGTCCCAGCTATTCGGGAGGCTG AAAATACAAAAAAAATAGCCAAGCGTGGTGGCGGGCGCCTGTAGTCCCAGCTATTCGGGAGGCTG A G APOC1P1 Ensembl:ENSG00000214855 Pseudogene exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1285021797 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9929786 26877 RMVar_ID_26877 Human_SNP_ID_667054276 A-to-I Human chr19 + 44931360 44931360 44931360 AAAAATAGCCAAGCGTGGTGGCAGGCGCCTGTAGTCCCAGCTATTCGGGAGGCTGAGGCAGGAGA AAAAATAGCCAAGCGTGGTGGCAGGCGCCTGTCGTCCCAGCTATTCGGGAGGCTGAGGCAGGAGA A C APOC1P1 Ensembl:ENSG00000214855 Pseudogene exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1171886481 Functional Loss SNV dbSNP153 33..33 33 - - - 26878 RMVar_ID_26878 Human_SNP_ID_667060174 A-to-I Human chr19 - 44950560 44950560 44950560 ATCGCTTGAGCCCAGGAATTGGAGACTAGCCTAGGCAACTTGACGAAACCCCGTCTCTACTAAAA ATCGCTTGAGCCCAGGAATTGGAGACTAGCCTCGGCAACTTGACGAAACCCCGTCTCTACTAAAA T G AC011481.1 Ensembl:ENSG00000267114 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1214423684 Functional Loss SNV dbSNP153 33..33 33 - - - 26879 RMVar_ID_26879 Human_SNP_ID_667068349 A-to-I Human chr19 + 44979073 44979073 44979073 ACTATCTCAGCTCACCACAATTTCCACCTCCCAAGTTCAAGCGATTCTCCCACCTTAGCCTCCAA ACTATCTCAGCTCACCACAATTTCCACCTCCCGAGTTCAAGCGATTCTCCCACCTTAGCCTCCAA A G CLPTM1 Ensembl:ENSG00000104853 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs945353807 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7756,RMVar_hsa_circ_59809 26880 RMVar_ID_26880 Human_SNP_ID_667069700 A-to-I Human chr19 + 44984262 44984262 44984262 CATCACCGAGCCTGTGCAGGCGCCCCATGTGTATTCAAACAGGCCCTGCCCCTACCCGCATTTCC CATCACCGAGCCTGTGCAGGCGCCCCATGTGTGTTCAAACAGGCCCTGCCCCTACCCGCATTTCC A G CLPTM1 Ensembl:ENSG00000104853 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs204473 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7756,RMVar_hsa_circ_59809 26881 RMVar_ID_26881 Human_SNP_ID_667069860 A-to-I Human chr19 + 44984861 44984861 44984861 GGCACCCGCCACCACATCCGGCTGATTTTTGTATTTTTATTAGAGACGGGGGGTTTCACCATGCT GGCACCCGCCACCACATCCGGCTGATTTTTGTGTTTTTATTAGAGACGGGGGGTTTCACCATGCT A G CLPTM1 Ensembl:ENSG00000104853 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1342905458 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7756,RMVar_hsa_circ_59809 26882 RMVar_ID_26882 Human_SNP_ID_111269639 A-to-I Human chr2 + 210008373 210008373 210008373 GCTGGAGTGCAGTGGCGTGATCTCAGCTCACTACAGTCTCCACCTCCTGGGTACAAGCGATCTTC GCTGGAGTGCAGTGGCGTGATCTCAGCTCACTGCAGTCTCCACCTCCTGGGTACAAGCGATCTTC A G RPE Ensembl:ENSG00000197713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1206890076 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9101818 RMVar_hsa_circ_3137,RMVar_hsa_circ_102112,RMVar_hsa_circ_206525 26883 RMVar_ID_26883 Human_SNP_ID_111274895 A-to-I Human chr2 - 210028299 210028299 210028299 TGAAGGAATGGGAAGGTGGAGAAGGTATTTACATAGGGATACGACAACAAAGGCACAGGACAAGT TGAAGGAATGGGAAGGTGGAGAAGGTATTTACGTAGGGATACGACAACAAAGGCACAGGACAAGT T C KANSL1L Ensembl:ENSG00000144445 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs866110772 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_68902,RMVar_hsa_circ_264810 26884 RMVar_ID_26884 Human_SNP_ID_111285142 A-to-I Human chr2 - 210071112 210071112 210071112 ACTCTGTTGCCCAGGCTGGAGTGCACTGGCACAATCTCAGCTCACTGCAACCTCCGCCTCCCGGG ACTCTGTTGCCCAGGCTGGAGTGCACTGGCACGATCTCAGCTCACTGCAACCTCCGCCTCCCGGG T C KANSL1L Ensembl:ENSG00000144445 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1177187373 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22159,RMVar_hsa_circ_68902,RMVar_hsa_circ_97517,RMVar_hsa_circ_206535,RMVar_hsa_circ_294960,RMVar_hsa_circ_308450,RMVar_hsa_circ_292926,RMVar_hsa_circ_206537,RMVar_hsa_circ_206538,RMVar_hsa_circ_319295 26885 RMVar_ID_26885 Human_SNP_ID_111298882 A-to-I Human chr2 - 210131848 210131848 210131848 TACTAAAAATACAATTAACTGGGTGTGGTGGTACATGCCTGTAATCCCAGCTACTCAGGAGGCTG TACTAAAAATACAATTAACTGGGTGTGGTGGTGCATGCCTGTAATCCCAGCTACTCAGGAGGCTG T C KANSL1L Ensembl:ENSG00000144445 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs184762257 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22159,RMVar_hsa_circ_206546,RMVar_hsa_circ_335925,RMVar_hsa_circ_206540,RMVar_hsa_circ_206548,RMVar_hsa_circ_292408,RMVar_hsa_circ_206547,RMVar_hsa_circ_206550,RMVar_hsa_circ_286510,RMVar_hsa_circ_206551,RMVar_hsa_circ_206549,RMVar_hsa_circ_283446 26886 RMVar_ID_26886 Human_SNP_ID_111303270 A-to-I Human chr2 - 210150540 210150540 210150540 GACCTCAGGTAATCTGCTGACCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCA GACCTCAGGTAATCTGCTGACCTTGGCCTCCCCAAGTGCTGGGATTACAGGCATGAGCCACCGCA T G KANSL1L Ensembl:ENSG00000144445 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs957978319 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22159,RMVar_hsa_circ_206546,RMVar_hsa_circ_335925,RMVar_hsa_circ_206540,RMVar_hsa_circ_206548,RMVar_hsa_circ_292408,RMVar_hsa_circ_206547,RMVar_hsa_circ_206550,RMVar_hsa_circ_286510,RMVar_hsa_circ_206551,RMVar_hsa_circ_206549,RMVar_hsa_circ_283446 26887 RMVar_ID_26887 Human_SNP_ID_111303308 A-to-I Human chr2 - 210150670 210150670 210150670 TCAAGCGATTCTCCTGCTTCAGCCTCCCAAGTAGCTGGGATTACAGGTGTGCACCACCACGCCCA TCAAGCGATTCTCCTGCTTCAGCCTCCCAAGTGGCTGGGATTACAGGTGTGCACCACCACGCCCA T C KANSL1L Ensembl:ENSG00000144445 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1038312680 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22159,RMVar_hsa_circ_206546,RMVar_hsa_circ_335925,RMVar_hsa_circ_206540,RMVar_hsa_circ_206548,RMVar_hsa_circ_292408,RMVar_hsa_circ_206547,RMVar_hsa_circ_206550,RMVar_hsa_circ_286510,RMVar_hsa_circ_206551,RMVar_hsa_circ_206549,RMVar_hsa_circ_283446 26888 RMVar_ID_26888 Human_SNP_ID_111303440 A-to-I Human chr2 - 210151108 210151108 210151108 GGGAGGCTAAGGCAGGAGAATTGCTTGAACCCAGGAGGTGGAGGTTGCAGTGAGCCCGTATCACC GGGAGGCTAAGGCAGGAGAATTGCTTGAACCCGGGAGGTGGAGGTTGCAGTGAGCCCGTATCACC T C KANSL1L Ensembl:ENSG00000144445 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1312025879 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22159,RMVar_hsa_circ_206546,RMVar_hsa_circ_335925,RMVar_hsa_circ_206540,RMVar_hsa_circ_206548,RMVar_hsa_circ_292408,RMVar_hsa_circ_206547,RMVar_hsa_circ_206550,RMVar_hsa_circ_286510,RMVar_hsa_circ_206551,RMVar_hsa_circ_206549,RMVar_hsa_circ_283446 26889 RMVar_ID_26889 Human_SNP_ID_111303956 A-to-I Human chr2 - 210153174 210153174 210153174 AATTTTTGTATTTTTCGTAGAGGCAAGGTTTCACCATGTTGGTCAGGCTGGTCTCGAACTCCTGA AATTTTTGTATTTTTCGTAGAGGCAAGGTTTCGCCATGTTGGTCAGGCTGGTCTCGAACTCCTGA T C KANSL1L Ensembl:ENSG00000144445 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs922952326 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_143968 RMVar_hsa_circ_22159,RMVar_hsa_circ_206546,RMVar_hsa_circ_335925,RMVar_hsa_circ_206540,RMVar_hsa_circ_206548,RMVar_hsa_circ_292408,RMVar_hsa_circ_206547,RMVar_hsa_circ_206550,RMVar_hsa_circ_286510,RMVar_hsa_circ_206551,RMVar_hsa_circ_206549,RMVar_hsa_circ_283446 26890 RMVar_ID_26890 Human_SNP_ID_111383601 A-to-I Human chr2 - 210475424 210475424 210475424 GGGAGGCTGAGGCGGGAGAATTGCTGGAGCCTAGGAGATTCGAGGCTGTAGTGAGCTATGATTGC GGGAGGCTGAGGCGGGAGAATTGCTGGAGCCTGGGAGATTCGAGGCTGTAGTGAGCTATGATTGC T C LANCL1 Ensembl:ENSG00000115365 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1468369042 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120643,RMVar_hsa_circ_206559,RMVar_hsa_circ_206561,RMVar_hsa_circ_344554,RMVar_hsa_circ_340868,RMVar_hsa_circ_206563,RMVar_hsa_circ_372109,RMVar_hsa_circ_206564 26891 RMVar_ID_26891 Human_SNP_ID_111383602 A-to-I Human chr2 - 210475424 210475424 210475424 GGGAGGCTGAGGCGGGAGAATTGCTGGAGCCTAGGAGATTCGAGGCTGTAGTGAGCTATGATTGC GGGAGGCTGAGGCGGGAGAATTGCTGGAGCCTCGGAGATTCGAGGCTGTAGTGAGCTATGATTGC T G LANCL1 Ensembl:ENSG00000115365 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1468369042 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120643,RMVar_hsa_circ_206559,RMVar_hsa_circ_206561,RMVar_hsa_circ_344554,RMVar_hsa_circ_340868,RMVar_hsa_circ_206563,RMVar_hsa_circ_372109,RMVar_hsa_circ_206564 26892 RMVar_ID_26892 Human_SNP_ID_111883123 A-to-I Human chr2 - 212397338 212397338 212397338 CTCTTGAGTAGCTGGGACTGCAGGAGCGTGCCACCATGCCTGGCTGTTTTGTATTTTTTGTAGAG CTCTTGAGTAGCTGGGACTGCAGGAGCGTGCCGCCATGCCTGGCTGTTTTGTATTTTTTGTAGAG T C ERBB4 Ensembl:ENSG00000178568 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs915283317 Functional Loss SNV dbSNP153 33..33 33 - - - 26893 RMVar_ID_26893 Human_SNP_ID_111885120 A-to-I Human chr2 - 212404988 212404987 212404988 ATATACCAAGGAATATTATGCAGCCATAAAAAAGAATGAGATCATGTATTTTGTGGGGACATGGA ATATACCAAGGAATATTATGCAGCCATAAAAA_GAATGAGATCATGTATTTTGTGGGGACATGGA CT C ERBB4 Ensembl:ENSG00000178568 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1464489923 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_22988447 26894 RMVar_ID_26894 Human_SNP_ID_112345242 A-to-I Human chr2 + 214280783 214280783 214280783 CCTGGGCGTCTTCTCATAGACTAGATTCTCTCATATAGCAGCATGAGCTTTCTTATACATCTCCT CCTGGGCGTCTTCTCATAGACTAGATTCTCTCCTATAGCAGCATGAGCTTTCTTATACATCTCCT A C SPAG16 Ensembl:ENSG00000144451 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs954026288 Functional Loss SNV dbSNP153 33..33 33 - - - 26895 RMVar_ID_26895 Human_SNP_ID_112603020 A-to-I Human chr2 + 215312889 215312889 215312889 GGGAGGCCGAGGTGGGCTGATCACTTACGGTCAAGAGTTCGAGACCAGCCTGGCCAACATGGTGA GGGAGGCCGAGGTGGGCTGATCACTTACGGTCGAGAGTTCGAGACCAGCCTGGCCAACATGGTGA A G ATIC Ensembl:ENSG00000138363 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1017125162 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25586108 RMVar_hsa_circ_12568,RMVar_hsa_circ_302872,RMVar_hsa_circ_316542,RMVar_hsa_circ_341411,RMVar_hsa_circ_347151,RMVar_hsa_circ_324815,RMVar_hsa_circ_310177,RMVar_hsa_circ_291045,RMVar_hsa_circ_291534,RMVar_hsa_circ_277267,RMVar_hsa_circ_206690,RMVar_hsa_circ_206692,RMVar_hsa_circ_206693,RMVar_hsa_circ_206694,RMVar_hsa_circ_206691,RMVar_hsa_circ_206688,RMVar_hsa_circ_206689 26896 RMVar_ID_26896 Human_SNP_ID_112603730 A-to-I Human chr2 + 215315496 215315496 215315496 CTTCCACCTCAGCCTCCTGAGTATCTGGGACTACAGCTGCACACCAGCATGCCCAACTAATTTTT CTTCCACCTCAGCCTCCTGAGTATCTGGGACTGCAGCTGCACACCAGCATGCCCAACTAATTTTT A G ATIC Ensembl:ENSG00000138363 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1161983796 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12568,RMVar_hsa_circ_302872,RMVar_hsa_circ_316542,RMVar_hsa_circ_341411,RMVar_hsa_circ_347151,RMVar_hsa_circ_324815,RMVar_hsa_circ_310177,RMVar_hsa_circ_291045,RMVar_hsa_circ_291534,RMVar_hsa_circ_277267,RMVar_hsa_circ_206690,RMVar_hsa_circ_206692,RMVar_hsa_circ_206693,RMVar_hsa_circ_206694,RMVar_hsa_circ_206691,RMVar_hsa_circ_206688,RMVar_hsa_circ_206689 26897 RMVar_ID_26897 Human_SNP_ID_112603779 A-to-I Human chr2 + 215315767 215315767 215315767 GAGGTCAGGAGTTTGAGCCCAGCCTGGCCAACATGGTGCAACTCCATCTCTGCTAAAAATACAAA GAGGTCAGGAGTTTGAGCCCAGCCTGGCCAACGTGGTGCAACTCCATCTCTGCTAAAAATACAAA A G ATIC Ensembl:ENSG00000138363 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1235972961 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12568,RMVar_hsa_circ_302872,RMVar_hsa_circ_316542,RMVar_hsa_circ_341411,RMVar_hsa_circ_347151,RMVar_hsa_circ_324815,RMVar_hsa_circ_310177,RMVar_hsa_circ_291045,RMVar_hsa_circ_291534,RMVar_hsa_circ_277267,RMVar_hsa_circ_206690,RMVar_hsa_circ_206692,RMVar_hsa_circ_206693,RMVar_hsa_circ_206694,RMVar_hsa_circ_206691,RMVar_hsa_circ_206688,RMVar_hsa_circ_206689 26898 RMVar_ID_26898 Human_SNP_ID_112604301 A-to-I Human chr2 + 215317625 215317625 215317625 CTCCTGCCTCAGCCTCCCCAGTAGCTGGGATTACAGGTGCCCGCCATCACGCTCGGCTAATTTTT CTCCTGCCTCAGCCTCCCCAGTAGCTGGGATTGCAGGTGCCCGCCATCACGCTCGGCTAATTTTT A G ATIC Ensembl:ENSG00000138363 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs376541399 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12568,RMVar_hsa_circ_302872,RMVar_hsa_circ_316542,RMVar_hsa_circ_341411,RMVar_hsa_circ_347151,RMVar_hsa_circ_324815,RMVar_hsa_circ_310177,RMVar_hsa_circ_291045,RMVar_hsa_circ_291534,RMVar_hsa_circ_277267,RMVar_hsa_circ_206690,RMVar_hsa_circ_206692,RMVar_hsa_circ_206693,RMVar_hsa_circ_206694,RMVar_hsa_circ_206691,RMVar_hsa_circ_206688,RMVar_hsa_circ_206689 26899 RMVar_ID_26899 Human_SNP_ID_112604680 A-to-I Human chr2 + 215318980 215318980 215318980 CTCGCTGCAGCCTCTGTCTGCTTCCCAGGCTCAAGCAGTTCTCCCACCTCAGCCTCCCAAGTAGC CTCGCTGCAGCCTCTGTCTGCTTCCCAGGCTCGAGCAGTTCTCCCACCTCAGCCTCCCAAGTAGC A G ATIC Ensembl:ENSG00000138363 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs529074078 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_302872,RMVar_hsa_circ_316542,RMVar_hsa_circ_341411,RMVar_hsa_circ_347151,RMVar_hsa_circ_324815,RMVar_hsa_circ_310177,RMVar_hsa_circ_291045,RMVar_hsa_circ_291534,RMVar_hsa_circ_277267,RMVar_hsa_circ_206690,RMVar_hsa_circ_206692,RMVar_hsa_circ_206693,RMVar_hsa_circ_206694,RMVar_hsa_circ_206691,RMVar_hsa_circ_206698,RMVar_hsa_circ_206688,RMVar_hsa_circ_206689,RMVar_hsa_circ_288676,RMVar_hsa_circ_365970,RMVar_hsa_circ_372796,RMVar_hsa_circ_94556,RMVar_hsa_circ_206696,RMVar_hsa_circ_206697,RMVar_hsa_circ_206695 26900 RMVar_ID_26900 Human_SNP_ID_112604682 A-to-I Human chr2 + 215318984 215318984 215318984 CTGCAGCCTCTGTCTGCTTCCCAGGCTCAAGCAGTTCTCCCACCTCAGCCTCCCAAGTAGCTGGG CTGCAGCCTCTGTCTGCTTCCCAGGCTCAAGCGGTTCTCCCACCTCAGCCTCCCAAGTAGCTGGG A G ATIC Ensembl:ENSG00000138363 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs60917883 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2771,GWAS_ID_2772 RMVar_hsa_circ_302872,RMVar_hsa_circ_316542,RMVar_hsa_circ_341411,RMVar_hsa_circ_347151,RMVar_hsa_circ_324815,RMVar_hsa_circ_310177,RMVar_hsa_circ_291045,RMVar_hsa_circ_291534,RMVar_hsa_circ_277267,RMVar_hsa_circ_206690,RMVar_hsa_circ_206692,RMVar_hsa_circ_206693,RMVar_hsa_circ_206694,RMVar_hsa_circ_206691,RMVar_hsa_circ_206698,RMVar_hsa_circ_206688,RMVar_hsa_circ_206689,RMVar_hsa_circ_288676,RMVar_hsa_circ_365970,RMVar_hsa_circ_372796,RMVar_hsa_circ_94556,RMVar_hsa_circ_206696,RMVar_hsa_circ_206697,RMVar_hsa_circ_206695 26901 RMVar_ID_26901 Human_SNP_ID_112609056 A-to-I Human chr2 + 215334258 215334258 215334258 CTCTGTTGCCCAGGCTGGAGTGCAGTGGCGCCATCTCAGCTCACTGCAACCTCCACCTCCTGGGT CTCTGTTGCCCAGGCTGGAGTGCAGTGGCGCCGTCTCAGCTCACTGCAACCTCCACCTCCTGGGT A G ATIC Ensembl:ENSG00000138363 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1304352684 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_341411,RMVar_hsa_circ_310177,RMVar_hsa_circ_291045,RMVar_hsa_circ_277267,RMVar_hsa_circ_206690,RMVar_hsa_circ_206691,RMVar_hsa_circ_206698,RMVar_hsa_circ_206688,RMVar_hsa_circ_206689,RMVar_hsa_circ_372796,RMVar_hsa_circ_48635,RMVar_hsa_circ_20216,RMVar_hsa_circ_345571,RMVar_hsa_circ_330270,RMVar_hsa_circ_206702,RMVar_hsa_circ_341820,RMVar_hsa_circ_29414,RMVar_hsa_circ_94858,RMVar_hsa_circ_311718,RMVar_hsa_circ_349382,RMVar_hsa_circ_339018,RMVar_hsa_circ_206704,RMVar_hsa_circ_206706,RMVar_hsa_circ_206705,RMVar_hsa_circ_347041,RMVar_hsa_circ_206710,RMVar_hsa_circ_63389 26902 RMVar_ID_26902 Human_SNP_ID_112609071 A-to-I Human chr2 + 215334298 215334298 215334298 TCACTGCAACCTCCACCTCCTGGGTTCAAGCGATTCTCCTGCCTCAGCGTCCTGAGTAGCTGGGA TCACTGCAACCTCCACCTCCTGGGTTCAAGCGGTTCTCCTGCCTCAGCGTCCTGAGTAGCTGGGA A G ATIC Ensembl:ENSG00000138363 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs931146193 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_341411,RMVar_hsa_circ_310177,RMVar_hsa_circ_291045,RMVar_hsa_circ_277267,RMVar_hsa_circ_206690,RMVar_hsa_circ_206691,RMVar_hsa_circ_206698,RMVar_hsa_circ_206688,RMVar_hsa_circ_206689,RMVar_hsa_circ_372796,RMVar_hsa_circ_48635,RMVar_hsa_circ_20216,RMVar_hsa_circ_345571,RMVar_hsa_circ_330270,RMVar_hsa_circ_206702,RMVar_hsa_circ_341820,RMVar_hsa_circ_29414,RMVar_hsa_circ_94858,RMVar_hsa_circ_311718,RMVar_hsa_circ_349382,RMVar_hsa_circ_339018,RMVar_hsa_circ_206704,RMVar_hsa_circ_206706,RMVar_hsa_circ_206705,RMVar_hsa_circ_347041,RMVar_hsa_circ_206710,RMVar_hsa_circ_63389 26903 RMVar_ID_26903 Human_SNP_ID_112609094 A-to-I Human chr2 + 215334359 215334359 215334359 GGGATTACAGGTGCGTGCCACCACACCTGGCTAATTTTTTTGTATTTTTAGTAGAGACATGGTTT GGGATTACAGGTGCGTGCCACCACACCTGGCTGATTTTTTTGTATTTTTAGTAGAGACATGGTTT A G ATIC Ensembl:ENSG00000138363 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1284082015 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_341411,RMVar_hsa_circ_310177,RMVar_hsa_circ_291045,RMVar_hsa_circ_277267,RMVar_hsa_circ_206690,RMVar_hsa_circ_206691,RMVar_hsa_circ_206698,RMVar_hsa_circ_206688,RMVar_hsa_circ_206689,RMVar_hsa_circ_372796,RMVar_hsa_circ_48635,RMVar_hsa_circ_20216,RMVar_hsa_circ_345571,RMVar_hsa_circ_330270,RMVar_hsa_circ_206702,RMVar_hsa_circ_341820,RMVar_hsa_circ_29414,RMVar_hsa_circ_94858,RMVar_hsa_circ_311718,RMVar_hsa_circ_349382,RMVar_hsa_circ_339018,RMVar_hsa_circ_206704,RMVar_hsa_circ_206706,RMVar_hsa_circ_206705,RMVar_hsa_circ_347041,RMVar_hsa_circ_206710,RMVar_hsa_circ_63389 26904 RMVar_ID_26904 Human_SNP_ID_112609108 A-to-I Human chr2 + 215334396 215334396 215334396 TTTTGTATTTTTAGTAGAGACATGGTTTCACCATGTTGGCCAGGCTGGTCTTGAGCTCCTGACCT TTTTGTATTTTTAGTAGAGACATGGTTTCACCGTGTTGGCCAGGCTGGTCTTGAGCTCCTGACCT A G ATIC Ensembl:ENSG00000138363 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1426637534 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_341411,RMVar_hsa_circ_310177,RMVar_hsa_circ_291045,RMVar_hsa_circ_277267,RMVar_hsa_circ_206690,RMVar_hsa_circ_206691,RMVar_hsa_circ_206698,RMVar_hsa_circ_206688,RMVar_hsa_circ_206689,RMVar_hsa_circ_372796,RMVar_hsa_circ_48635,RMVar_hsa_circ_20216,RMVar_hsa_circ_345571,RMVar_hsa_circ_330270,RMVar_hsa_circ_206702,RMVar_hsa_circ_341820,RMVar_hsa_circ_29414,RMVar_hsa_circ_94858,RMVar_hsa_circ_311718,RMVar_hsa_circ_349382,RMVar_hsa_circ_339018,RMVar_hsa_circ_206704,RMVar_hsa_circ_206706,RMVar_hsa_circ_206705,RMVar_hsa_circ_347041,RMVar_hsa_circ_206710,RMVar_hsa_circ_63389 26905 RMVar_ID_26905 Human_SNP_ID_112610347 A-to-I Human chr2 + 215339171 215339171 215339171 TGTATAAATGGGATCATGTCTTCCATAATCTGACTCCTGTAACTTGGCTTTTTTCCATGTGCTAG TGTATAAATGGGATCATGTCTTCCATAATCTGGCTCCTGTAACTTGGCTTTTTTCCATGTGCTAG A G ATIC Ensembl:ENSG00000138363 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1568872 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_291045,RMVar_hsa_circ_277267,RMVar_hsa_circ_206698,RMVar_hsa_circ_206688,RMVar_hsa_circ_206689,RMVar_hsa_circ_372796,RMVar_hsa_circ_29414,RMVar_hsa_circ_94858,RMVar_hsa_circ_339018,RMVar_hsa_circ_206704,RMVar_hsa_circ_206705,RMVar_hsa_circ_63389,RMVar_hsa_circ_206711,RMVar_hsa_circ_358458,RMVar_hsa_circ_5222,RMVar_hsa_circ_307537,RMVar_hsa_circ_58808 26906 RMVar_ID_26906 Human_SNP_ID_112613362 A-to-I Human chr2 + 215349978 215349978 215349978 GAGGACATGGCACAAGTCACTGTGTACAGGCCACACTTAAGGACTGGGAGTTATACCCATCTTAA GAGGACATGGCACAAGTCACTGTGTACAGGCCGCACTTAAGGACTGGGAGTTATACCCATCTTAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs960802286 Functional Loss SNV dbSNP153 33..33 33 - - - 26907 RMVar_ID_26907 Human_SNP_ID_112619277 A-to-I Human chr2 - 215371786 215371786 215371786 CTTCATGGCCGGGTGTGATGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGTGG CTTCATGGCCGGGTGTGATGGCTCACGCCTGTTATCCCAGCACTTTGGGAGGCCGAGGCAGGTGG T A FN1 Ensembl:ENSG00000115414 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1188377362 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16018,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_365157 26908 RMVar_ID_26908 Human_SNP_ID_112620645 A-to-I Human chr2 - 215376615 215376615 215376615 TGACAGATGCTACTGAGACCACCATCACCATTAGCTGGAGAACCAAGACTGAGACGATCACTGGC TGACAGATGCTACTGAGACCACCATCACCATTGGCTGGAGAACCAAGACTGAGACGATCACTGGC T C FN1 Ensembl:ENSG00000115414 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1258010093 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_142068,Human_RBP_ID_921712,Human_RBP_ID_26820409 Human_Splice_Rec_355092,Human_Splice_Rec_355184,Human_Splice_Rec_355274,Human_Splice_Rec_355364,Human_Splice_Rec_355452,Human_Splice_Rec_355540,Human_Splice_Rec_355574,Human_Splice_Rec_355664,Human_Splice_Rec_355752,Human_Splice_Rec_355842,Human_Splice_Rec_355930,Human_Splice_Rec_355970,Human_Splice_Rec_356026 Human_miRNA_ID_1541899,Human_miRNA_ID_1595300 RMVar_hsa_circ_3650,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_63624,RMVar_hsa_circ_79478,RMVar_hsa_circ_55828,RMVar_hsa_circ_325049,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_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_206726,RMVar_hsa_circ_206724,RMVar_hsa_circ_380,RMVar_hsa_circ_120836,RMVar_hsa_circ_93135,RMVar_hsa_circ_121202,RMVar_hsa_circ_123710,RMVar_hsa_circ_99058,RMVar_hsa_circ_206728,RMVar_hsa_circ_206730,RMVar_hsa_circ_206731,RMVar_hsa_circ_206729,RMVar_hsa_circ_123745,RMVar_hsa_circ_82975,RMVar_hsa_circ_113512,RMVar_hsa_circ_54402,RMVar_hsa_circ_206733,RMVar_hsa_circ_206734,RMVar_hsa_circ_206735,RMVar_hsa_circ_206732 26909 RMVar_ID_26909 Human_SNP_ID_112758710 A-to-I Human chr2 - 215943683 215943683 215943683 GCGCGTGCCACCACACCTGGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTAG GCGCGTGCCACCACACCTGGCTAATTTTTTGTGTTTTTAGTAGAGACGGGGTTTCACCATGTTAG T C MREG Ensembl:ENSG00000118242 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1359888441 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93943,RMVar_hsa_circ_206796 26910 RMVar_ID_26910 Human_SNP_ID_112758723 A-to-I Human chr2 - 215943758 215943758 215943758 CGGCTCACTGCAACCTCCGCCTTCCGGTTTCAAGTGATTCCCCTGCCTCAGCCTCTGGAGTAGCT CGGCTCACTGCAACCTCCGCCTTCCGGTTTCAGGTGATTCCCCTGCCTCAGCCTCTGGAGTAGCT T C MREG Ensembl:ENSG00000118242 Protein coding 3'UTR GSE38233;GSE100210;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,cerebellum - 24183664,29129909,30559470 RNA-Seq:(High) rs1488245566 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93943,RMVar_hsa_circ_206796 26911 RMVar_ID_26911 Human_SNP_ID_112758734 A-to-I Human chr2 - 215943803 215943803 215943803 GGACTCTCGCTCTGTCGCCCAGGCTGGAGTACAGTGGTGCGATCTCGGCTCACTGCAACCTCCGC GGACTCTCGCTCTGTCGCCCAGGCTGGAGTACGGTGGTGCGATCTCGGCTCACTGCAACCTCCGC T C MREG Ensembl:ENSG00000118242 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs559703685 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93943,RMVar_hsa_circ_206796 26912 RMVar_ID_26912 Human_SNP_ID_112782188 A-to-I Human chr2 - 216038862 216038862 216038862 CCAGCACTTTGGGAGGCCGAGGTAGGCGGGTCAGTTGAGGTCAGGAGTTCAAGACCAGGCTGGCC CCAGCACTTTGGGAGGCCGAGGTAGGCGGGTCTGTTGAGGTCAGGAGTTCAAGACCAGGCTGGCC T A PECR Ensembl:ENSG00000115425 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1250991224 Functional Loss SNV dbSNP153 33..33 33 - - - 26913 RMVar_ID_26913 Human_SNP_ID_112782610 A-to-I Human chr2 - 216040526 216040526 216040526 TCAGGGGCTGGGCACCATGGCTCACACCTGTAATCTCAGCACTTTGGGAGGCAAAGGTGGGCCAA TCAGGGGCTGGGCACCATGGCTCACACCTGTAGTCTCAGCACTTTGGGAGGCAAAGGTGGGCCAA T C PECR Ensembl:ENSG00000115425 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs548363883 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17570173 RMVar_hsa_circ_206797,RMVar_hsa_circ_275754,RMVar_hsa_circ_285303,RMVar_hsa_circ_358707,RMVar_hsa_circ_311057,RMVar_hsa_circ_278163,RMVar_hsa_circ_206799,RMVar_hsa_circ_206800,RMVar_hsa_circ_206798 26914 RMVar_ID_26914 Human_SNP_ID_112782667 A-to-I Human chr2 - 216040795 216040795 216040795 ATGATTTCGGCTCACTGCAATCTCTGCCTCCCAGGTTCAAGCAATTCTCCTGCCTCAGGATCCAG ATGATTTCGGCTCACTGCAATCTCTGCCTCCCGGGTTCAAGCAATTCTCCTGCCTCAGGATCCAG T C PECR Ensembl:ENSG00000115425 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1401142366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18754371 RMVar_hsa_circ_206797,RMVar_hsa_circ_275754,RMVar_hsa_circ_285303,RMVar_hsa_circ_358707,RMVar_hsa_circ_311057,RMVar_hsa_circ_278163,RMVar_hsa_circ_206799,RMVar_hsa_circ_206800,RMVar_hsa_circ_206798 26915 RMVar_ID_26915 Human_SNP_ID_112800413 A-to-I Human chr2 + 216109524 216109524 216109524 GACTGGGGATCCGGAGAGGGTGGTTCGGAAGCAGGAATCGTGGGATCGCGGTCAAGACAAAGAAT GACTGGGGATCCGGAGAGGGTGGTTCGGAAGCGGGAATCGTGGGATCGCGGTCAAGACAAAGAAT A G XRCC5 Ensembl:ENSG00000079246 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1362840488 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1068014,Human_RBP_ID_5378106,Human_RBP_ID_13766075,Human_RBP_ID_19098653,Human_RBP_ID_20617445,Human_RBP_ID_22360160,Human_RBP_ID_23852502,Human_RBP_ID_25513351 26916 RMVar_ID_26916 Human_SNP_ID_112825864 A-to-I Human chr2 + 216208974 216208974 216208974 GGCGAAACCCCATCTCTACTAAAAATACAAAAAATTAGCCGGGTGTGGTGGTGGGCGCCTGTAAT GGCGAAACCCCATCTCTACTAAAAATACAAAAGATTAGCCGGGTGTGGTGGTGGGCGCCTGTAAT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1290589427 Functional Loss SNV dbSNP153 33..33 33 - - - 26917 RMVar_ID_26917 Human_SNP_ID_112825865 A-to-I Human chr2 + 216208978 216208978 216208978 AAACCCCATCTCTACTAAAAATACAAAAAATTAGCCGGGTGTGGTGGTGGGCGCCTGTAATACCC AAACCCCATCTCTACTAAAAATACAAAAAATTTGCCGGGTGTGGTGGTGGGCGCCTGTAATACCC A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs373099991 Functional Loss SNV dbSNP153 33..33 33 - - - 26918 RMVar_ID_26918 Human_SNP_ID_112826874 A-to-I Human chr2 - 216213341 216213341 216213341 TTACAATGACCTGTAATTCCATTTTGATTAAAAGCTTTGAGCCTTTGAACATCTTTGACAAATGT TTACAATGACCTGTAATTCCATTTTGATTAAAGGCTTTGAGCCTTTGAACATCTTTGACAAATGT T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1305317386 Functional Loss SNV dbSNP153 33..33 33 - - - 26919 RMVar_ID_26919 Human_SNP_ID_112890428 A-to-I Human chr2 + 216472190 216472190 216472190 CAGCCTGGACAACATGGCGGAACCCCATCTCTACTAAGAATACAAAAATTAGCTGGGCATAGTGG CAGCCTGGACAACATGGCGGAACCCCATCTCTGCTAAGAATACAAAAATTAGCTGGGCATAGTGG A G SMARCAL1 Ensembl:ENSG00000138375 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs934976695 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_362545,RMVar_hsa_circ_275564,RMVar_hsa_circ_324724,RMVar_hsa_circ_206856,RMVar_hsa_circ_206858,RMVar_hsa_circ_300829,RMVar_hsa_circ_206857 26920 RMVar_ID_26920 Human_SNP_ID_112891054 A-to-I Human chr2 + 216474716 216474716 216474716 GGGCGGAGGTTGCCGTGAGCCAAGATCGTGCCACTGCACTCCAGCCTGAGTGACAAGAGTGAAAC GGGCGGAGGTTGCCGTGAGCCAAGATCGTGCCGCTGCACTCCAGCCTGAGTGACAAGAGTGAAAC A G SMARCAL1 Ensembl:ENSG00000138375 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941063626 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_362545,RMVar_hsa_circ_275564,RMVar_hsa_circ_324724,RMVar_hsa_circ_206856,RMVar_hsa_circ_206858,RMVar_hsa_circ_300829,RMVar_hsa_circ_206857 26921 RMVar_ID_26921 Human_SNP_ID_112891055 A-to-I Human chr2 + 216474716 216474716 216474716 GGGCGGAGGTTGCCGTGAGCCAAGATCGTGCCACTGCACTCCAGCCTGAGTGACAAGAGTGAAAC GGGCGGAGGTTGCCGTGAGCCAAGATCGTGCCTCTGCACTCCAGCCTGAGTGACAAGAGTGAAAC A T SMARCAL1 Ensembl:ENSG00000138375 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941063626 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_362545,RMVar_hsa_circ_275564,RMVar_hsa_circ_324724,RMVar_hsa_circ_206856,RMVar_hsa_circ_206858,RMVar_hsa_circ_300829,RMVar_hsa_circ_206857 26922 RMVar_ID_26922 Human_SNP_ID_112893163 A-to-I Human chr2 - 216483825 216483825 216483825 CTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCATGCACCACCATACCAGACTAATTTTG CTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTGCAGGCATGCACCACCATACCAGACTAATTTTG T C AC098820.4,AC098820.2 Ensembl:ENSG00000241520,Ensembl:ENSG00000232485 lincRNA,lincRNA exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1211214670 Functional Loss SNV dbSNP153 33..33 33 - - - 26923 RMVar_ID_26923 Human_SNP_ID_112897691 A-to-I Human chr2 + 216501811 216501811 216501811 CCAGTCTTGGCCCACTTCAACCTCCACTTCTTAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTG CCAGTCTTGGCCCACTTCAACCTCCACTTCTTCGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTG A C RPL37A Ensembl:ENSG00000197756 Protein coding 3'UTR GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line - 24183664,31158229 RNA-Seq:(High) rs1188685150 Functional Loss SNV dbSNP153 33..33 33 - - - 26924 RMVar_ID_26924 Human_SNP_ID_112897701 A-to-I Human chr2 + 216501857 216501857 216501857 CTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCACGCACCACCATACCTGGCTAATTTTT CTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTGCAGGCACGCACCACCATACCTGGCTAATTTTT A G RPL37A Ensembl:ENSG00000197756 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1344705061 Functional Loss SNV dbSNP153 33..33 33 - - - 26925 RMVar_ID_26925 Human_SNP_ID_112897711 A-to-I Human chr2 + 216501875 216501875 216501875 GAGTAGCTGGGATTACAGGCACGCACCACCATACCTGGCTAATTTTTGTATTTTGAGTAGAGATG GAGTAGCTGGGATTACAGGCACGCACCACCATGCCTGGCTAATTTTTGTATTTTGAGTAGAGATG A G RPL37A Ensembl:ENSG00000197756 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs765538226 Functional Loss SNV dbSNP153 33..33 33 - - - 26926 RMVar_ID_26926 Human_SNP_ID_112897715 A-to-I Human chr2 + 216501883 216501883 216501883 GGGATTACAGGCACGCACCACCATACCTGGCTAATTTTTGTATTTTGAGTAGAGATGGAGTTTTC GGGATTACAGGCACGCACCACCATACCTGGCTGATTTTTGTATTTTGAGTAGAGATGGAGTTTTC A G RPL37A Ensembl:ENSG00000197756 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1559145772 Functional Loss SNV dbSNP153 33..33 33 - - - 26927 RMVar_ID_26927 Human_SNP_ID_112897716 A-to-I Human chr2 + 216501903 216501903 216501903 CCATACCTGGCTAATTTTTGTATTTTGAGTAGAGATGGAGTTTTCACCACATTGGCCAGGCTGTT CCATACCTGGCTAATTTTTGTATTTTGAGTAGTGATGGAGTTTTCACCACATTGGCCAGGCTGTT A T RPL37A Ensembl:ENSG00000197756 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1421632391 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_544068,Human_RBP_ID_2623185 26928 RMVar_ID_26928 Human_SNP_ID_112897743 A-to-I Human chr2 + 216501999 216501997 216501999 TGGCCTTCCAGAGTGCTGGGATTACAGGTGTGAGCCACCACGCCCAGCCTTGCATTTAATATTTT TGGCCTTCCAGAGTGCTGGGATTACAGGTGT__GCCACCACGCCCAGCCTTGCATTTAATATTTT TGA T RPL37A Ensembl:ENSG00000197756 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1425796234 Functional Loss DEL dbSNP153 32..33 33 - - - 26929 RMVar_ID_26929 Human_SNP_ID_112897756 A-to-I Human chr2 + 216502035 216502032 216502035 ACCACGCCCAGCCTTGCATTTAATATTTTTATAATGTGTCTAGGCTGGGTGCGGTGACTCACGCC ACCACGCCCAGCCTTGCATTTAATATTTTT___ATGTGTCTAGGCTGGGTGCGGTGACTCACGCC TATA T RPL37A Ensembl:ENSG00000197756 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs371446015 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_544069 26930 RMVar_ID_26930 Human_SNP_ID_112897757 A-to-I Human chr2 + 216502035 216502035 216502035 ACCACGCCCAGCCTTGCATTTAATATTTTTATAATGTGTCTAGGCTGGGTGCGGTGACTCACGCC ACCACGCCCAGCCTTGCATTTAATATTTTTATTATGTGTCTAGGCTGGGTGCGGTGACTCACGCC A T RPL37A Ensembl:ENSG00000197756 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs923591254 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_544069 26931 RMVar_ID_26931 Human_SNP_ID_112897778 A-to-I Human chr2 + 216502098 216502098 216502098 CCTGAAATCCCAGCACTTTGGGTGGCTGAGGCAGGTGGATTACTTGAGGCCAGGAGATTGAGACC CCTGAAATCCCAGCACTTTGGGTGGCTGAGGCGGGTGGATTACTTGAGGCCAGGAGATTGAGACC A G RPL37A Ensembl:ENSG00000197756 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1178943126 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4595926,Human_RBP_ID_8512211,Human_RBP_ID_17570179 26932 RMVar_ID_26932 Human_SNP_ID_112897779 A-to-I Human chr2 + 216502098 216502098 216502098 CCTGAAATCCCAGCACTTTGGGTGGCTGAGGCAGGTGGATTACTTGAGGCCAGGAGATTGAGACC CCTGAAATCCCAGCACTTTGGGTGGCTGAGGCTGGTGGATTACTTGAGGCCAGGAGATTGAGACC A T RPL37A Ensembl:ENSG00000197756 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1178943126 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4595926,Human_RBP_ID_8512211,Human_RBP_ID_17570179 26933 RMVar_ID_26933 Human_SNP_ID_112897787 A-to-I Human chr2 + 216502143 216502142 216502144 GAGGCCAGGAGATTGAGACCAGTGTGGCCAACATAGCAAAAACCCGTCTCGACGAAAAATACAAA GAGGCCAGGAGATTGAGACCAGTGTGGCCAAC__AGCAAAAACCCGTCTCGACGAAAAATACAAA CAT C RPL37A Ensembl:ENSG00000197756 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1241210233 Functional Loss DEL dbSNP153 33..34 33 - - - 26934 RMVar_ID_26934 Human_SNP_ID_112897788 A-to-I Human chr2 + 216502143 216502143 216502143 GAGGCCAGGAGATTGAGACCAGTGTGGCCAACATAGCAAAAACCCGTCTCGACGAAAAATACAAA GAGGCCAGGAGATTGAGACCAGTGTGGCCAACGTAGCAAAAACCCGTCTCGACGAAAAATACAAA A G RPL37A Ensembl:ENSG00000197756 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1047117133 Functional Loss SNV dbSNP153 33..33 33 - - - 26935 RMVar_ID_26935 Human_SNP_ID_112897803 A-to-I Human chr2 - 216502170 216502170 216502170 GGCATGTGCCACCATACCAAGCTATTTTTTGTATTTTTCGTCGAGACGGGTTTTTGCTATGTTGG GGCATGTGCCACCATACCAAGCTATTTTTTGTGTTTTTCGTCGAGACGGGTTTTTGCTATGTTGG T C - - Other Unknown GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1247936234 Functional Loss SNV dbSNP153 33..33 33 - - - 26936 RMVar_ID_26936 Human_SNP_ID_112897804 A-to-I Human chr2 + 216502171 216502171 216502171 CAACATAGCAAAAACCCGTCTCGACGAAAAATACAAAAAATAGCTTGGTATGGTGGCACATGCCT CAACATAGCAAAAACCCGTCTCGACGAAAAATGCAAAAAATAGCTTGGTATGGTGGCACATGCCT A G RPL37A Ensembl:ENSG00000197756 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs555735838 Functional Loss SNV dbSNP153 33..33 33 - - - 26937 RMVar_ID_26937 Human_SNP_ID_112897806 A-to-I Human chr2 + 216502173 216502173 216502173 ACATAGCAAAAACCCGTCTCGACGAAAAATACAAAAAATAGCTTGGTATGGTGGCACATGCCTGT ACATAGCAAAAACCCGTCTCGACGAAAAATACCAAAAATAGCTTGGTATGGTGGCACATGCCTGT A C RPL37A Ensembl:ENSG00000197756 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229,31158229 RNA-Seq:(High) rs577356493 Functional Loss SNV dbSNP153 33..33 33 - - - 26938 RMVar_ID_26938 Human_SNP_ID_112897807 A-to-I Human chr2 + 216502173 216502173 216502173 ACATAGCAAAAACCCGTCTCGACGAAAAATACAAAAAATAGCTTGGTATGGTGGCACATGCCTGT ACATAGCAAAAACCCGTCTCGACGAAAAATACGAAAAATAGCTTGGTATGGTGGCACATGCCTGT A G RPL37A Ensembl:ENSG00000197756 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229,31158229 RNA-Seq:(High) rs577356493 Functional Loss SNV dbSNP153 33..33 33 - - - 26939 RMVar_ID_26939 Human_SNP_ID_112897808 A-to-I Human chr2 + 216502173 216502173 216502173 ACATAGCAAAAACCCGTCTCGACGAAAAATACAAAAAATAGCTTGGTATGGTGGCACATGCCTGT ACATAGCAAAAACCCGTCTCGACGAAAAATACTAAAAATAGCTTGGTATGGTGGCACATGCCTGT A T RPL37A Ensembl:ENSG00000197756 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229,31158229 RNA-Seq:(High) rs577356493 Functional Loss SNV dbSNP153 33..33 33 - - - 26940 RMVar_ID_26940 Human_SNP_ID_112897810 A-to-I Human chr2 + 216502180 216502180 216502180 AAAAACCCGTCTCGACGAAAAATACAAAAAATAGCTTGGTATGGTGGCACATGCCTGTAATCCCA AAAAACCCGTCTCGACGAAAAATACAAAAAATTGCTTGGTATGGTGGCACATGCCTGTAATCCCA A T RPL37A Ensembl:ENSG00000197756 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1218559702 Functional Loss SNV dbSNP153 33..33 33 - - - 26941 RMVar_ID_26941 Human_SNP_ID_112897813 A-to-I Human chr2 + 216502188 216502188 216502188 GTCTCGACGAAAAATACAAAAAATAGCTTGGTATGGTGGCACATGCCTGTAATCCCAGCTACTTT GTCTCGACGAAAAATACAAAAAATAGCTTGGTGTGGTGGCACATGCCTGTAATCCCAGCTACTTT A G RPL37A Ensembl:ENSG00000197756 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs144312540 Functional Loss SNV dbSNP153 33..33 33 - - - 26942 RMVar_ID_26942 Human_SNP_ID_112897814 A-to-I Human chr2 + 216502198 216502191 216502198 AAAATACAAAAAATAGCTTGGTATGGTGGCACATGCCTGTAATCCCAGCTACTTTGGAGGCTCAG AAAATACAAAAAATAGCTTGGTATGG_______TGCCTGTAATCCCAGCTACTTTGGAGGCTCAG GTGGCACA G RPL37A Ensembl:ENSG00000197756 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs201453908 Functional Loss DEL dbSNP153 27..33 33 - - - 26943 RMVar_ID_26943 Human_SNP_ID_112897817 A-to-I Human chr2 + 216502198 216502198 216502198 AAAATACAAAAAATAGCTTGGTATGGTGGCACATGCCTGTAATCCCAGCTACTTTGGAGGCTCAG AAAATACAAAAAATAGCTTGGTATGGTGGCACGTGCCTGTAATCCCAGCTACTTTGGAGGCTCAG A G RPL37A Ensembl:ENSG00000197756 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs1167086042 Functional Loss SNV dbSNP153 33..33 33 - - - 26944 RMVar_ID_26944 Human_SNP_ID_112897831 A-to-I Human chr2 + 216502235 216502235 216502235 TGTAATCCCAGCTACTTTGGAGGCTCAGGCACAAGAATCACTTGAACCTACGAGGCGGAGGTTGC TGTAATCCCAGCTACTTTGGAGGCTCAGGCACGAGAATCACTTGAACCTACGAGGCGGAGGTTGC A G RPL37A Ensembl:ENSG00000197756 Protein coding 3'UTR GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-Seq:(High) rs1006217128 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23310617,Human_RBP_ID_27477557 26945 RMVar_ID_26945 Human_SNP_ID_112898264 A-to-I Human chr2 + 216503534 216503534 216503534 CTCGTGCCTCAGCCTCCGAAGTAGCTGGGATTACAGGCTTATGCCACAAAGCTCAGCTAGTTTTT CTCGTGCCTCAGCCTCCGAAGTAGCTGGGATTGCAGGCTTATGCCACAAAGCTCAGCTAGTTTTT A G RPL37A Ensembl:ENSG00000197756 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1470390933 Functional Loss SNV dbSNP153 33..33 33 - - - 26946 RMVar_ID_26946 Human_SNP_ID_112898291 A-to-I Human chr2 + 216503602 216503602 216503602 TTTTTTATTTTTAGTAGAGATGGGCTTTCGCCATGTTGACCAGGCTGGTCTCAAACTCCCAGGCT TTTTTTATTTTTAGTAGAGATGGGCTTTCGCCGTGTTGACCAGGCTGGTCTCAAACTCCCAGGCT A G RPL37A Ensembl:ENSG00000197756 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1052881466 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13770179 26947 RMVar_ID_26947 Human_SNP_ID_112898995 A-to-I Human chr2 + 216505872 216505872 216505872 TTGAGTTAGGGTCTGGCTCTGTCGTCCAGGCTAGAGTGCAGTGGTGTGGTCTCAGCTCACTGCAA TTGAGTTAGGGTCTGGCTCTGTCGTCCAGGCTGGAGTGCAGTGGTGTGGTCTCAGCTCACTGCAA A G RPL37A Ensembl:ENSG00000197756 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1161305084 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13770306 26948 RMVar_ID_26948 Human_SNP_ID_112904659 A-to-I Human chr2 + 216528505 216528505 216528505 TGAACTTCCTGGCATCCAGAACTATAAGGAATAAATTTATGTTGTTTAAGTCACCCAGTCTTTGG TGAACTTCCTGGCATCCAGAACTATAAGGAATGAATTTATGTTGTTTAAGTCACCCAGTCTTTGG A G RPL37A Ensembl:ENSG00000197756 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1460008919 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3615893,Human_RBP_ID_13771293 26949 RMVar_ID_26949 Human_SNP_ID_112923853 A-to-I Human chr2 - 216610480 216610480 216610480 TGTGAGTCCCTCTGGGAACCCAACATGGATCCAGAACACCCGTTTGAAACCATCTCCCCAGCCAT TGTGAGTCCCTCTGGGAACCCAACATGGATCCGGAACACCCGTTTGAAACCATCTCCCCAGCCAT T C PSMB3P2 Ensembl:ENSG00000235444 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1347054045 Functional Loss SNV dbSNP153 33..33 33 - - - 26950 RMVar_ID_26950 Human_SNP_ID_112923857 A-to-I Human chr2 - 216610495 216610495 216610495 CAAATGTACGGAATGTGTGAGTCCCTCTGGGAACCCAACATGGATCCAGAACACCCGTTTGAAAC CAAATGTACGGAATGTGTGAGTCCCTCTGGGAGCCCAACATGGATCCAGAACACCCGTTTGAAAC T C PSMB3P2 Ensembl:ENSG00000235444 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1289977514 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26479706 26951 RMVar_ID_26951 Human_SNP_ID_112923961 A-to-I Human chr2 - 216610929 216610929 216610929 TCATGTCTATTATGTCCTATAACGGAGGAGCCATCATGGCCATGAAGGGGAAGAACCGTGTGGCC TCATGTCTATTATGTCCTATAACGGAGGAGCCGTCATGGCCATGAAGGGGAAGAACCGTGTGGCC T C PSMB3P2 Ensembl:ENSG00000235444 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1351516850 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1839059,Human_miRNA_ID_1855166 26952 RMVar_ID_26952 Human_SNP_ID_113326847 A-to-I Human chr2 + 218226249 218226249 218226249 GGGAGGCAGGAGTTGCTGTGAGCTGAGATCACACCACTGCACTCCAGCCTGGGCGATACAGTGAG GGGAGGCAGGAGTTGCTGTGAGCTGAGATCACGCCACTGCACTCCAGCCTGGGCGATACAGTGAG A G ARPC2 Ensembl:ENSG00000163466 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs186856859 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25586282 RMVar_hsa_circ_54730,RMVar_hsa_circ_306182,RMVar_hsa_circ_28944,RMVar_hsa_circ_50413 26953 RMVar_ID_26953 Human_SNP_ID_113327192 A-to-I Human chr2 + 218227455 218227455 218227455 ATATTTGTTTTGTTTTTTTGAGACTGAGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGCGTT ATATTTGTTTTGTTTTTTTGAGACTGAGTCTCGCTCTGTCACCCAGGCTGGAGTGCAGTGGCGTT A G ARPC2 Ensembl:ENSG00000163466 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs897916251 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54730,RMVar_hsa_circ_306182,RMVar_hsa_circ_28944,RMVar_hsa_circ_50413 26954 RMVar_ID_26954 Human_SNP_ID_113327212 A-to-I Human chr2 + 218227526 218227526 218227526 CTGCTCACTGCCGCCTCCACCTCCCCGAGTTCAAGCGATTCTCCTGCCTCCGCCTCTCAAGTAGC CTGCTCACTGCCGCCTCCACCTCCCCGAGTTCCAGCGATTCTCCTGCCTCCGCCTCTCAAGTAGC A C ARPC2 Ensembl:ENSG00000163466 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs867687348 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54730,RMVar_hsa_circ_306182,RMVar_hsa_circ_28944,RMVar_hsa_circ_50413 26955 RMVar_ID_26955 Human_SNP_ID_113327501 A-to-I Human chr2 + 218228555 218228555 218228555 AGCTTTGTAATTTTAAGAAAGAGCAAAGAAACAAGTGCTCAGCAATTCTATCCCAGTGTTTCTGC AGCTTTGTAATTTTAAGAAAGAGCAAAGAAACGAGTGCTCAGCAATTCTATCCCAGTGTTTCTGC A G ARPC2 Ensembl:ENSG00000163466 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2063711 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54730,RMVar_hsa_circ_306182,RMVar_hsa_circ_28944,RMVar_hsa_circ_50413 26956 RMVar_ID_26956 Human_SNP_ID_113328420 A-to-I Human chr2 + 218232114 218232114 218232114 AATATAAAAATTAGCTTGGTGTGGTGGTGGACACCTGTAATCCCAGCTACTAGGGAGGCTGAGGC AATATAAAAATTAGCTTGGTGTGGTGGTGGACGCCTGTAATCCCAGCTACTAGGGAGGCTGAGGC A G ARPC2 Ensembl:ENSG00000163466 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs922146398 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25296,RMVar_hsa_circ_306182,RMVar_hsa_circ_28944,RMVar_hsa_circ_50413,RMVar_hsa_circ_295956,RMVar_hsa_circ_318119,RMVar_hsa_circ_371792,RMVar_hsa_circ_47512,RMVar_hsa_circ_206889 26957 RMVar_ID_26957 Human_SNP_ID_113328895 A-to-I Human chr2 + 218233907 218233907 218233907 AGATTCTCGGCCAGGCATAGTGGCTCATGCCTATAATCCCAGCACTTTGGGAGGACGAGGCGGGT AGATTCTCGGCCAGGCATAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGACGAGGCGGGT A G ARPC2 Ensembl:ENSG00000163466 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459800441 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25296,RMVar_hsa_circ_306182,RMVar_hsa_circ_28944,RMVar_hsa_circ_50413,RMVar_hsa_circ_295956,RMVar_hsa_circ_318119,RMVar_hsa_circ_371792,RMVar_hsa_circ_47512,RMVar_hsa_circ_206889 26958 RMVar_ID_26958 Human_SNP_ID_113329219 A-to-I Human chr2 + 218235216 218235216 218235216 CTATTTTTTCAGACAGTCTCATTCTGTTGCCCAGGCTGGAATGCAGTGGTACAGTCATAGCTCAC CTATTTTTTCAGACAGTCTCATTCTGTTGCCCGGGCTGGAATGCAGTGGTACAGTCATAGCTCAC A G ARPC2 Ensembl:ENSG00000163466 Protein coding exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1231035303 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_357886 RMVar_hsa_circ_306182,RMVar_hsa_circ_28944,RMVar_hsa_circ_50413,RMVar_hsa_circ_295956,RMVar_hsa_circ_318119,RMVar_hsa_circ_47512,RMVar_hsa_circ_206891,RMVar_hsa_circ_332187,RMVar_hsa_circ_364844,RMVar_hsa_circ_311817,RMVar_hsa_circ_206890 26959 RMVar_ID_26959 Human_SNP_ID_113329223 A-to-I Human chr2 + 218235228 218235228 218235228 ACAGTCTCATTCTGTTGCCCAGGCTGGAATGCAGTGGTACAGTCATAGCTCACTGCAGCCTCCTC ACAGTCTCATTCTGTTGCCCAGGCTGGAATGCGGTGGTACAGTCATAGCTCACTGCAGCCTCCTC A G ARPC2 Ensembl:ENSG00000163466 Protein coding exon GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs139498093 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_357886 RMVar_hsa_circ_306182,RMVar_hsa_circ_28944,RMVar_hsa_circ_50413,RMVar_hsa_circ_295956,RMVar_hsa_circ_318119,RMVar_hsa_circ_47512,RMVar_hsa_circ_206891,RMVar_hsa_circ_332187,RMVar_hsa_circ_364844,RMVar_hsa_circ_311817,RMVar_hsa_circ_206890 26960 RMVar_ID_26960 Human_SNP_ID_113329228 A-to-I Human chr2 + 218235275 218235275 218235275 GCTCACTGCAGCCTCCTCCAAATCTTGGGCTCAAGCAATCCTCCCGCTTTAGCCTCTCCGGTAGC GCTCACTGCAGCCTCCTCCAAATCTTGGGCTCGAGCAATCCTCCCGCTTTAGCCTCTCCGGTAGC A G ARPC2 Ensembl:ENSG00000163466 Protein coding exon GSE47997;GSE100210;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611827,GSM3611828,GSM3611829 K562 cells&HepG2 cells;HepG2 cell line;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BEP2D cell line - 23474544,29129909,29129909,31158229,31158229 RNA-Seq:(High) rs938622006 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_357886 RMVar_hsa_circ_306182,RMVar_hsa_circ_28944,RMVar_hsa_circ_50413,RMVar_hsa_circ_295956,RMVar_hsa_circ_318119,RMVar_hsa_circ_47512,RMVar_hsa_circ_206891,RMVar_hsa_circ_332187,RMVar_hsa_circ_364844,RMVar_hsa_circ_311817,RMVar_hsa_circ_206890 26961 RMVar_ID_26961 Human_SNP_ID_113329229 A-to-I Human chr2 + 218235279 218235279 218235279 ACTGCAGCCTCCTCCAAATCTTGGGCTCAAGCAATCCTCCCGCTTTAGCCTCTCCGGTAGCTGGG ACTGCAGCCTCCTCCAAATCTTGGGCTCAAGCTATCCTCCCGCTTTAGCCTCTCCGGTAGCTGGG A T ARPC2 Ensembl:ENSG00000163466 Protein coding exon GSE47997;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,29129909,31158229,32596459 RNA-Seq:(High) rs1348247299 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_357886 RMVar_hsa_circ_306182,RMVar_hsa_circ_28944,RMVar_hsa_circ_50413,RMVar_hsa_circ_295956,RMVar_hsa_circ_318119,RMVar_hsa_circ_47512,RMVar_hsa_circ_206891,RMVar_hsa_circ_332187,RMVar_hsa_circ_364844,RMVar_hsa_circ_311817,RMVar_hsa_circ_206890 26962 RMVar_ID_26962 Human_SNP_ID_113329368 A-to-I Human chr2 + 218235861 218235861 218235861 TGTAATCCCAGCACTTTGGGGAGGCCAAGGTGAGTGAATTGCTTGAGCTCAGAAGTTCAGGACCA TGTAATCCCAGCACTTTGGGGAGGCCAAGGTGGGTGAATTGCTTGAGCTCAGAAGTTCAGGACCA A G ARPC2 Ensembl:ENSG00000163466 Protein coding intron GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs1390613986 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_306182,RMVar_hsa_circ_28944,RMVar_hsa_circ_50413,RMVar_hsa_circ_295956,RMVar_hsa_circ_318119,RMVar_hsa_circ_47512,RMVar_hsa_circ_206891,RMVar_hsa_circ_332187,RMVar_hsa_circ_364844,RMVar_hsa_circ_311817,RMVar_hsa_circ_206890 26963 RMVar_ID_26963 Human_SNP_ID_113329382 A-to-I Human chr2 + 218235934 218235934 218235934 AGCATAATGAGATACCTGTCTCTATAAAAAATACAGAAATTAGCCAGGCATGGTGGCAGCCACCT AGCATAATGAGATACCTGTCTCTATAAAAAATGCAGAAATTAGCCAGGCATGGTGGCAGCCACCT A G ARPC2 Ensembl:ENSG00000163466 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1003936533 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25514267 RMVar_hsa_circ_306182,RMVar_hsa_circ_28944,RMVar_hsa_circ_50413,RMVar_hsa_circ_295956,RMVar_hsa_circ_318119,RMVar_hsa_circ_47512,RMVar_hsa_circ_206891,RMVar_hsa_circ_332187,RMVar_hsa_circ_364844,RMVar_hsa_circ_311817,RMVar_hsa_circ_206890 26964 RMVar_ID_26964 Human_SNP_ID_113329385 A-to-I Human chr2 + 218235969 218235969 218235969 GAAATTAGCCAGGCATGGTGGCAGCCACCTGTAATACCAGGTACTCAGGTGGCTGAAGCACGAGA GAAATTAGCCAGGCATGGTGGCAGCCACCTGTGATACCAGGTACTCAGGTGGCTGAAGCACGAGA A G ARPC2 Ensembl:ENSG00000163466 Protein coding intron GSE38233;GSE100210;GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,29129909,32596459 RNA-Seq:(High) rs1292378848 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_306182,RMVar_hsa_circ_28944,RMVar_hsa_circ_50413,RMVar_hsa_circ_295956,RMVar_hsa_circ_318119,RMVar_hsa_circ_47512,RMVar_hsa_circ_206891,RMVar_hsa_circ_332187,RMVar_hsa_circ_364844,RMVar_hsa_circ_311817,RMVar_hsa_circ_206890 26965 RMVar_ID_26965 Human_SNP_ID_113329389 A-to-I Human chr2 + 218235983 218235983 218235983 ATGGTGGCAGCCACCTGTAATACCAGGTACTCAGGTGGCTGAAGCACGAGAATCGCTTGAACCCA ATGGTGGCAGCCACCTGTAATACCAGGTACTCGGGTGGCTGAAGCACGAGAATCGCTTGAACCCA A G ARPC2 Ensembl:ENSG00000163466 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1138153 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_306182,RMVar_hsa_circ_28944,RMVar_hsa_circ_50413,RMVar_hsa_circ_295956,RMVar_hsa_circ_318119,RMVar_hsa_circ_47512,RMVar_hsa_circ_206891,RMVar_hsa_circ_332187,RMVar_hsa_circ_364844,RMVar_hsa_circ_311817,RMVar_hsa_circ_206890 26966 RMVar_ID_26966 Human_SNP_ID_113329400 A-to-I Human chr2 + 218236031 218236031 218236031 AGAATCGCTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCTGAGATTGCGCCACTGCCCTCTAGCC AGAATCGCTTGAACCCAGGAGGCAGAGGTTGCGGTGAGCTGAGATTGCGCCACTGCCCTCTAGCC A G ARPC2 Ensembl:ENSG00000163466 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs968647481 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_306182,RMVar_hsa_circ_28944,RMVar_hsa_circ_50413,RMVar_hsa_circ_295956,RMVar_hsa_circ_318119,RMVar_hsa_circ_47512,RMVar_hsa_circ_206891,RMVar_hsa_circ_332187,RMVar_hsa_circ_364844,RMVar_hsa_circ_311817,RMVar_hsa_circ_206890 26967 RMVar_ID_26967 Human_SNP_ID_113329488 A-to-I Human chr2 + 218236404 218236404 218236404 CCAAAATAGAATGATGATTGATATTATTTAATACTGGAGTGCCTCTCCAGTATTAAATAAAATGT CCAAAATAGAATGATGATTGATATTATTTAATGCTGGAGTGCCTCTCCAGTATTAAATAAAATGT A G ARPC2 Ensembl:ENSG00000163466 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs915703378 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6887905 Human_Splice_Rec_357988 RMVar_hsa_circ_306182,RMVar_hsa_circ_28944,RMVar_hsa_circ_50413,RMVar_hsa_circ_295956,RMVar_hsa_circ_318119,RMVar_hsa_circ_47512,RMVar_hsa_circ_206891,RMVar_hsa_circ_332187,RMVar_hsa_circ_364844,RMVar_hsa_circ_311817,RMVar_hsa_circ_206890 26968 RMVar_ID_26968 Human_SNP_ID_113329527 A-to-I Human chr2 + 218236549 218236549 218236549 GCGCGGTGGCTTATGCCTGTAATCCCAGCACTATCGGAGGCCAGGGCGGGCGGATCACCTGCATT GCGCGGTGGCTTATGCCTGTAATCCCAGCACTGTCGGAGGCCAGGGCGGGCGGATCACCTGCATT A G ARPC2 Ensembl:ENSG00000163466 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1247711972 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25514275 RMVar_hsa_circ_306182,RMVar_hsa_circ_28944,RMVar_hsa_circ_50413,RMVar_hsa_circ_295956,RMVar_hsa_circ_318119,RMVar_hsa_circ_47512,RMVar_hsa_circ_206891,RMVar_hsa_circ_332187,RMVar_hsa_circ_364844,RMVar_hsa_circ_311817,RMVar_hsa_circ_206890 26969 RMVar_ID_26969 Human_SNP_ID_113329549 A-to-I Human chr2 + 218236628 218236628 218236628 CAGCATGACCAACATGGAGAAACCCCGTCTCTACTAAAAGTACAAAATTAGCCAGGCCTGGTGGC CAGCATGACCAACATGGAGAAACCCCGTCTCTGCTAAAAGTACAAAATTAGCCAGGCCTGGTGGC A G ARPC2 Ensembl:ENSG00000163466 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1329708755 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_306182,RMVar_hsa_circ_28944,RMVar_hsa_circ_50413,RMVar_hsa_circ_295956,RMVar_hsa_circ_318119,RMVar_hsa_circ_47512,RMVar_hsa_circ_206891,RMVar_hsa_circ_332187,RMVar_hsa_circ_364844,RMVar_hsa_circ_311817,RMVar_hsa_circ_206890 26970 RMVar_ID_26970 Human_SNP_ID_113329551 A-to-I Human chr2 + 218236631 218236631 218236631 CATGACCAACATGGAGAAACCCCGTCTCTACTAAAAGTACAAAATTAGCCAGGCCTGGTGGCGCA CATGACCAACATGGAGAAACCCCGTCTCTACTGAAAGTACAAAATTAGCCAGGCCTGGTGGCGCA A G ARPC2 Ensembl:ENSG00000163466 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs778132724 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_306182,RMVar_hsa_circ_28944,RMVar_hsa_circ_50413,RMVar_hsa_circ_295956,RMVar_hsa_circ_318119,RMVar_hsa_circ_47512,RMVar_hsa_circ_206891,RMVar_hsa_circ_332187,RMVar_hsa_circ_364844,RMVar_hsa_circ_311817,RMVar_hsa_circ_206890 26971 RMVar_ID_26971 Human_SNP_ID_113329749 A-to-I Human chr2 + 218237361 218237361 218237361 ACCTGGGACCACAGGCGTGTACCACCACACCCAGCTAATTTTGTATTTTTATTAGAGACGGGGTT ACCTGGGACCACAGGCGTGTACCACCACACCCGGCTAATTTTGTATTTTTATTAGAGACGGGGTT A G ARPC2 Ensembl:ENSG00000163466 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs996009953 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_306182,RMVar_hsa_circ_28944,RMVar_hsa_circ_50413,RMVar_hsa_circ_295956,RMVar_hsa_circ_318119,RMVar_hsa_circ_47512,RMVar_hsa_circ_206891,RMVar_hsa_circ_332187,RMVar_hsa_circ_364844,RMVar_hsa_circ_311817,RMVar_hsa_circ_206890 26972 RMVar_ID_26972 Human_SNP_ID_113329846 A-to-I Human chr2 + 218237666 218237666 218237666 TCAGCTCGCTGTAACCTCCACCTCCTGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGC TCAGCTCGCTGTAACCTCCACCTCCTGGGTTCGAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGC A G ARPC2 Ensembl:ENSG00000163466 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs992212048 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_306182,RMVar_hsa_circ_28944,RMVar_hsa_circ_50413,RMVar_hsa_circ_295956,RMVar_hsa_circ_318119,RMVar_hsa_circ_47512,RMVar_hsa_circ_206891,RMVar_hsa_circ_332187,RMVar_hsa_circ_364844,RMVar_hsa_circ_311817,RMVar_hsa_circ_206890 26973 RMVar_ID_26973 Human_SNP_ID_113329847 A-to-I Human chr2 + 218237670 218237670 218237670 CTCGCTGTAACCTCCACCTCCTGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGCTAGG CTCGCTGTAACCTCCACCTCCTGGGTTCAAGCTATTCTCCTGCCTCAGCCTCCCAAGTAGCTAGG A T ARPC2 Ensembl:ENSG00000163466 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1399660559 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_306182,RMVar_hsa_circ_28944,RMVar_hsa_circ_50413,RMVar_hsa_circ_295956,RMVar_hsa_circ_318119,RMVar_hsa_circ_47512,RMVar_hsa_circ_206891,RMVar_hsa_circ_332187,RMVar_hsa_circ_364844,RMVar_hsa_circ_311817,RMVar_hsa_circ_206890 26974 RMVar_ID_26974 Human_SNP_ID_113330421 A-to-I Human chr2 + 218239776 218239776 218239776 CCACCACACCCAGCTAATTTTGTATTTTTAGTAGAGACGGGGTTTCTCCATGTTGGTCAGGCTGG CCACCACACCCAGCTAATTTTGTATTTTTAGTGGAGACGGGGTTTCTCCATGTTGGTCAGGCTGG A G ARPC2 Ensembl:ENSG00000163466 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1421525186 Functional Loss SNV dbSNP153 33..33 33 - - - 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 26975 RMVar_ID_26975 Human_SNP_ID_113330443 A-to-I Human chr2 + 218239865 218239865 218239865 TGCCCATCTCGGCCTCCCAAAGTGCTGGTATTACAGGCATGAGCCACCATGCCCAGCCTTGACGT TGCCCATCTCGGCCTCCCAAAGTGCTGGTATTGCAGGCATGAGCCACCATGCCCAGCCTTGACGT A G ARPC2 Ensembl:ENSG00000163466 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1467318903 Functional Loss SNV dbSNP153 33..33 33 - - - 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 26976 RMVar_ID_26976 Human_SNP_ID_113332073 A-to-I Human chr2 + 218246729 218246729 218246729 ACAGTGGCTCACACCTGTAATCCCAGCACTTTAAGAGGCCAAGGCGAGCAGATCACTTGAGGTCA ACAGTGGCTCACACCTGTAATCCCAGCACTTTCAGAGGCCAAGGCGAGCAGATCACTTGAGGTCA A C ARPC2 Ensembl:ENSG00000163466 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1187149625 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50413,RMVar_hsa_circ_47512,RMVar_hsa_circ_206892,RMVar_hsa_circ_206891,RMVar_hsa_circ_364844,RMVar_hsa_circ_337918,RMVar_hsa_circ_21239,RMVar_hsa_circ_206897,RMVar_hsa_circ_102665,RMVar_hsa_circ_206896,RMVar_hsa_circ_106380,RMVar_hsa_circ_374102,RMVar_hsa_circ_206895,RMVar_hsa_circ_308565,RMVar_hsa_circ_206898,RMVar_hsa_circ_206899 26977 RMVar_ID_26977 Human_SNP_ID_113332130 A-to-I Human chr2 + 218246897 218246897 218246897 CTACTCGGGCAAGCGAGGCATGGCAATTGCTTAAACCCAGAAAGTGGAGGTTGCAGCAAGCCGAG CTACTCGGGCAAGCGAGGCATGGCAATTGCTTGAACCCAGAAAGTGGAGGTTGCAGCAAGCCGAG A G ARPC2 Ensembl:ENSG00000163466 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1163235013 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50413,RMVar_hsa_circ_47512,RMVar_hsa_circ_206892,RMVar_hsa_circ_206891,RMVar_hsa_circ_364844,RMVar_hsa_circ_337918,RMVar_hsa_circ_21239,RMVar_hsa_circ_206897,RMVar_hsa_circ_102665,RMVar_hsa_circ_206896,RMVar_hsa_circ_106380,RMVar_hsa_circ_374102,RMVar_hsa_circ_206895,RMVar_hsa_circ_308565,RMVar_hsa_circ_206898,RMVar_hsa_circ_206899 26978 RMVar_ID_26978 Human_SNP_ID_113332391 A-to-I Human chr2 + 218247887 218247887 218247887 ATGGCGTGAACCTGGGAGGCGGAGCTTGCAATAGGCCAAGATCACGCGACTGCACTCCAGCCTGG ATGGCGTGAACCTGGGAGGCGGAGCTTGCAATGGGCCAAGATCACGCGACTGCACTCCAGCCTGG A G ARPC2 Ensembl:ENSG00000163466 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1212965619 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13772306,Human_RBP_ID_25514357 RMVar_hsa_circ_50413,RMVar_hsa_circ_47512,RMVar_hsa_circ_206892,RMVar_hsa_circ_206891,RMVar_hsa_circ_364844,RMVar_hsa_circ_337918,RMVar_hsa_circ_21239,RMVar_hsa_circ_206897,RMVar_hsa_circ_102665,RMVar_hsa_circ_206896,RMVar_hsa_circ_106380,RMVar_hsa_circ_374102,RMVar_hsa_circ_206895,RMVar_hsa_circ_308565,RMVar_hsa_circ_206898,RMVar_hsa_circ_206899 26979 RMVar_ID_26979 Human_SNP_ID_113333288 A-to-I Human chr2 + 218251036 218251036 218251036 TTTTTGTATTTTAGTAGAGATGGGGTTTCACCATGTTGCCCAGGCTGGTCTAGAACTCGTGAGCT TTTTTGTATTTTAGTAGAGATGGGGTTTCACCGTGTTGCCCAGGCTGGTCTAGAACTCGTGAGCT A G ARPC2 Ensembl:ENSG00000163466 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1364389519 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102665,RMVar_hsa_circ_206896,RMVar_hsa_circ_106380,RMVar_hsa_circ_206898,RMVar_hsa_circ_206899 26980 RMVar_ID_26980 Human_SNP_ID_113333453 A-to-I Human chr2 + 218251619 218251619 218251619 GGGACCACAGGCATGCACCATCACAGCTGGCTAATTTTTGTATTTTTGTAGAGACGGGATTTCAC GGGACCACAGGCATGCACCATCACAGCTGGCTGATTTTTGTATTTTTGTAGAGACGGGATTTCAC A G ARPC2 Ensembl:ENSG00000163466 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1559484959 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102665,RMVar_hsa_circ_206896,RMVar_hsa_circ_106380,RMVar_hsa_circ_206898,RMVar_hsa_circ_206899 26981 RMVar_ID_26981 Human_SNP_ID_113333559 A-to-I Human chr2 + 218252076 218252076 218252076 AGAAACCCCATCTCTACTAAAAATACAGAATTAGCTAGGCATGGTAGTGCATGCCTGTAATCCCA AGAAACCCCATCTCTACTAAAAATACAGAATTCGCTAGGCATGGTAGTGCATGCCTGTAATCCCA A C ARPC2 Ensembl:ENSG00000163466 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1442688846 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102665,RMVar_hsa_circ_206896,RMVar_hsa_circ_106380,RMVar_hsa_circ_206898,RMVar_hsa_circ_206899 26982 RMVar_ID_26982 Human_SNP_ID_113333648 A-to-I Human chr2 + 218252434 218252434 218252434 GAGAGGATGTGCTTGCTGCCTCTCCAGAACCTAGTCTCCATCCTGGTGTCTACATTTTCCCCTTT GAGAGGATGTGCTTGCTGCCTCTCCAGAACCTGGTCTCCATCCTGGTGTCTACATTTTCCCCTTT A G ARPC2 Ensembl:ENSG00000163466 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs907981 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102665,RMVar_hsa_circ_206896,RMVar_hsa_circ_106380,RMVar_hsa_circ_206898,RMVar_hsa_circ_206899 26983 RMVar_ID_26983 Human_SNP_ID_113361781 A-to-I Human chr2 + 218359742 218359742 218359742 GTGCACTGTTTTTGAACTTTATATTGCATCATAACACGACTGCTATTCTTCAGCTTCACTGTGTA GTGCACTGTTTTTGAACTTTATATTGCATCATGACACGACTGCTATTCTTCAGCTTCACTGTGTA A G CATIP Ensembl:ENSG00000158428 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs144311907 Functional Loss SNV dbSNP153 33..33 33 - - - 26984 RMVar_ID_26984 Human_SNP_ID_113373421 A-to-I Human chr2 + 218398897 218398897 218398897 CTTGCAGCGAGAAGACAGGGACCTCCGTTCCCAAGTGCCCAGCACTGCGCCACAGGCCGGGTGGA CTTGCAGCGAGAAGACAGGGACCTCCGTTCCCGAGTGCCCAGCACTGCGCCACAGGCCGGGTGGA A G CTDSP1 Ensembl:ENSG00000144579 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs999907381 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9331278 26985 RMVar_ID_26985 Human_SNP_ID_113399031 A-to-I Human chr2 - 218493006 218493006 218493006 TGAATATGAGGGAAAAAAATTTTTTTTTTTTTAAGACAGAGTCTTGCTCTGTCACCCAGGCTGGA TGAATATGAGGGAAAAAAATTTTTTTTTTTTTGAGACAGAGTCTTGCTCTGTCACCCAGGCTGGA T C USP37 Ensembl:ENSG00000135913 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1026629649 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25514539 RMVar_hsa_circ_879,RMVar_hsa_circ_72545,RMVar_hsa_circ_109995,RMVar_hsa_circ_104950,RMVar_hsa_circ_206933,RMVar_hsa_circ_80152,RMVar_hsa_circ_206934,RMVar_hsa_circ_206932,RMVar_hsa_circ_106207,RMVar_hsa_circ_268323,RMVar_hsa_circ_93006,RMVar_hsa_circ_206938,RMVar_hsa_circ_24764,RMVar_hsa_circ_311363,RMVar_hsa_circ_206939,RMVar_hsa_circ_359894,RMVar_hsa_circ_206940,RMVar_hsa_circ_359442,RMVar_hsa_circ_586,RMVar_hsa_circ_60414,RMVar_hsa_circ_12241,RMVar_hsa_circ_358567,RMVar_hsa_circ_371824,RMVar_hsa_circ_274891,RMVar_hsa_circ_15303,RMVar_hsa_circ_40773,RMVar_hsa_circ_308324,RMVar_hsa_circ_206948,RMVar_hsa_circ_353180,RMVar_hsa_circ_34886,RMVar_hsa_circ_206950,RMVar_hsa_circ_266541,RMVar_hsa_circ_371770,RMVar_hsa_circ_43151,RMVar_hsa_circ_28284,RMVar_hsa_circ_206953,RMVar_hsa_circ_206954,RMVar_hsa_circ_206955,RMVar_hsa_circ_276442,RMVar_hsa_circ_299678,RMVar_hsa_circ_350978,RMVar_hsa_circ_40011,RMVar_hsa_circ_206956 26986 RMVar_ID_26986 Human_SNP_ID_113399945 A-to-I Human chr2 - 218496786 218496786 218496786 AAATTAGCCAGGCGTGATGTCGCATGTCTGTAATCCCAGCTACTTGGGAGGCTGATGCAGGATAA AAATTAGCCAGGCGTGATGTCGCATGTCTGTAGTCCCAGCTACTTGGGAGGCTGATGCAGGATAA T C USP37 Ensembl:ENSG00000135913 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1305725045 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_879,RMVar_hsa_circ_72545,RMVar_hsa_circ_109995,RMVar_hsa_circ_104950,RMVar_hsa_circ_206933,RMVar_hsa_circ_80152,RMVar_hsa_circ_206934,RMVar_hsa_circ_206932,RMVar_hsa_circ_106207,RMVar_hsa_circ_268323,RMVar_hsa_circ_93006,RMVar_hsa_circ_206938,RMVar_hsa_circ_24764,RMVar_hsa_circ_206939,RMVar_hsa_circ_359894,RMVar_hsa_circ_586,RMVar_hsa_circ_60414,RMVar_hsa_circ_12241,RMVar_hsa_circ_371824,RMVar_hsa_circ_274891,RMVar_hsa_circ_15303,RMVar_hsa_circ_40773,RMVar_hsa_circ_206948,RMVar_hsa_circ_34886,RMVar_hsa_circ_266541,RMVar_hsa_circ_371770,RMVar_hsa_circ_43151,RMVar_hsa_circ_28284,RMVar_hsa_circ_206953,RMVar_hsa_circ_206954,RMVar_hsa_circ_206955,RMVar_hsa_circ_299678,RMVar_hsa_circ_350978,RMVar_hsa_circ_40011,RMVar_hsa_circ_23734,RMVar_hsa_circ_290044,RMVar_hsa_circ_368219,RMVar_hsa_circ_357240,RMVar_hsa_circ_47380,RMVar_hsa_circ_206957 26987 RMVar_ID_26987 Human_SNP_ID_113400839 A-to-I Human chr2 - 218500600 218500600 218500600 AGGCTGAGGCAGGTGAATCACTTGAGGTCAGGAGTTCGAGAGCAGCCTGGCCAACATGGGGAAAC AGGCTGAGGCAGGTGAATCACTTGAGGTCAGGGGTTCGAGAGCAGCCTGGCCAACATGGGGAAAC T C USP37 Ensembl:ENSG00000135913 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1193700905 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_879,RMVar_hsa_circ_72545,RMVar_hsa_circ_104950,RMVar_hsa_circ_206933,RMVar_hsa_circ_80152,RMVar_hsa_circ_206934,RMVar_hsa_circ_106207,RMVar_hsa_circ_268323,RMVar_hsa_circ_93006,RMVar_hsa_circ_206938,RMVar_hsa_circ_206939,RMVar_hsa_circ_359894,RMVar_hsa_circ_60414,RMVar_hsa_circ_12241,RMVar_hsa_circ_371824,RMVar_hsa_circ_274891,RMVar_hsa_circ_15303,RMVar_hsa_circ_40773,RMVar_hsa_circ_206948,RMVar_hsa_circ_34886,RMVar_hsa_circ_266541,RMVar_hsa_circ_371770,RMVar_hsa_circ_27333,RMVar_hsa_circ_28284,RMVar_hsa_circ_206954,RMVar_hsa_circ_206955,RMVar_hsa_circ_350978,RMVar_hsa_circ_40011,RMVar_hsa_circ_23734,RMVar_hsa_circ_368219,RMVar_hsa_circ_357240,RMVar_hsa_circ_47380,RMVar_hsa_circ_280371,RMVar_hsa_circ_378790,RMVar_hsa_circ_49796,RMVar_hsa_circ_206961,RMVar_hsa_circ_206959,RMVar_hsa_circ_206960,RMVar_hsa_circ_265120 26988 RMVar_ID_26988 Human_SNP_ID_113406943 A-to-I Human chr2 - 218526408 218526408 218526408 CAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAAAATTAGCTGGGCGTGGTGGCAGGTGC CAACATGGTGAAACCCCATCTCTACTAAAAATGCAAAAAAATTAGCTGGGCGTGGTGGCAGGTGC T C USP37 Ensembl:ENSG00000135913 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs757442746 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104950,RMVar_hsa_circ_206933,RMVar_hsa_circ_80152,RMVar_hsa_circ_206934,RMVar_hsa_circ_106207,RMVar_hsa_circ_268323,RMVar_hsa_circ_206938,RMVar_hsa_circ_359894,RMVar_hsa_circ_60414,RMVar_hsa_circ_12241,RMVar_hsa_circ_274891,RMVar_hsa_circ_15303,RMVar_hsa_circ_40773,RMVar_hsa_circ_34886,RMVar_hsa_circ_266541,RMVar_hsa_circ_371770,RMVar_hsa_circ_27333,RMVar_hsa_circ_28284,RMVar_hsa_circ_206954,RMVar_hsa_circ_206955,RMVar_hsa_circ_350978,RMVar_hsa_circ_40011,RMVar_hsa_circ_23734,RMVar_hsa_circ_357240,RMVar_hsa_circ_47380,RMVar_hsa_circ_280371,RMVar_hsa_circ_378790,RMVar_hsa_circ_49796,RMVar_hsa_circ_206962,RMVar_hsa_circ_206959,RMVar_hsa_circ_206960,RMVar_hsa_circ_265120,RMVar_hsa_circ_297632,RMVar_hsa_circ_325551,RMVar_hsa_circ_359207,RMVar_hsa_circ_303996,RMVar_hsa_circ_206964,RMVar_hsa_circ_206965,RMVar_hsa_circ_206963 26989 RMVar_ID_26989 Human_SNP_ID_113407393 A-to-I Human chr2 - 218528155 218528155 218528155 CTGTATCGCCCAGGCTGGAGGACAGTAGGGCAATCTCGGCTGACTGCAACCTCTGCCTTCTGGGT CTGTATCGCCCAGGCTGGAGGACAGTAGGGCAGTCTCGGCTGACTGCAACCTCTGCCTTCTGGGT T C USP37 Ensembl:ENSG00000135913 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs867404104 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17570183 RMVar_hsa_circ_104950,RMVar_hsa_circ_206933,RMVar_hsa_circ_80152,RMVar_hsa_circ_206934,RMVar_hsa_circ_106207,RMVar_hsa_circ_268323,RMVar_hsa_circ_206938,RMVar_hsa_circ_359894,RMVar_hsa_circ_60414,RMVar_hsa_circ_12241,RMVar_hsa_circ_274891,RMVar_hsa_circ_15303,RMVar_hsa_circ_40773,RMVar_hsa_circ_34886,RMVar_hsa_circ_266541,RMVar_hsa_circ_371770,RMVar_hsa_circ_27333,RMVar_hsa_circ_28284,RMVar_hsa_circ_206954,RMVar_hsa_circ_206955,RMVar_hsa_circ_350978,RMVar_hsa_circ_40011,RMVar_hsa_circ_23734,RMVar_hsa_circ_357240,RMVar_hsa_circ_47380,RMVar_hsa_circ_280371,RMVar_hsa_circ_378790,RMVar_hsa_circ_49796,RMVar_hsa_circ_206962,RMVar_hsa_circ_206959,RMVar_hsa_circ_206960,RMVar_hsa_circ_265120,RMVar_hsa_circ_297632,RMVar_hsa_circ_325551,RMVar_hsa_circ_359207,RMVar_hsa_circ_303996,RMVar_hsa_circ_206964,RMVar_hsa_circ_206965,RMVar_hsa_circ_206963 26990 RMVar_ID_26990 Human_SNP_ID_113407814 A-to-I Human chr2 - 218529545 218529545 218529545 ACGATCCTCCCACCTCAGCCTTCCAAAGTGCTAGGGTTATAAGTGTTGAACCACTGCTCCTGCTC ACGATCCTCCCACCTCAGCCTTCCAAAGTGCTGGGGTTATAAGTGTTGAACCACTGCTCCTGCTC T C USP37 Ensembl:ENSG00000135913 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1019624813 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104950,RMVar_hsa_circ_206933,RMVar_hsa_circ_80152,RMVar_hsa_circ_206934,RMVar_hsa_circ_106207,RMVar_hsa_circ_268323,RMVar_hsa_circ_206938,RMVar_hsa_circ_359894,RMVar_hsa_circ_60414,RMVar_hsa_circ_12241,RMVar_hsa_circ_274891,RMVar_hsa_circ_15303,RMVar_hsa_circ_40773,RMVar_hsa_circ_34886,RMVar_hsa_circ_266541,RMVar_hsa_circ_371770,RMVar_hsa_circ_27333,RMVar_hsa_circ_28284,RMVar_hsa_circ_206954,RMVar_hsa_circ_206955,RMVar_hsa_circ_350978,RMVar_hsa_circ_40011,RMVar_hsa_circ_23734,RMVar_hsa_circ_357240,RMVar_hsa_circ_47380,RMVar_hsa_circ_280371,RMVar_hsa_circ_378790,RMVar_hsa_circ_49796,RMVar_hsa_circ_206962,RMVar_hsa_circ_206959,RMVar_hsa_circ_206960,RMVar_hsa_circ_265120,RMVar_hsa_circ_297632,RMVar_hsa_circ_325551,RMVar_hsa_circ_359207,RMVar_hsa_circ_303996,RMVar_hsa_circ_206964,RMVar_hsa_circ_206965,RMVar_hsa_circ_206963 26991 RMVar_ID_26991 Human_SNP_ID_113417968 A-to-I Human chr2 + 218571294 218571294 218571294 AAATGAGAATGTAAGCCGGGTGGTGTGTGCCCATAGTCCCAGCTACTTGGGAGGCTAAGGAGGGA AAATGAGAATGTAAGCCGGGTGGTGTGTGCCCGTAGTCCCAGCTACTTGGGAGGCTAAGGAGGGA A G CNOT9 Ensembl:ENSG00000144580 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1182224350 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25514721 RMVar_hsa_circ_89564,RMVar_hsa_circ_123323,RMVar_hsa_circ_206983,RMVar_hsa_circ_206984 26992 RMVar_ID_26992 Human_SNP_ID_113418038 A-to-I Human chr2 + 218571594 218571593 218571595 GCTTTTGTGATTCTTTTTTTTTTTTTTGAGATAGAGTTTTGCTCTTGTTGCCCAGGCTGGTGTGC GCTTTTGTGATTCTTTTTTTTTTTTTTGAGAT__AGTTTTGCTCTTGTTGCCCAGGCTGGTGTGC TAG T CNOT9 Ensembl:ENSG00000144580 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1374434096 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_89564,RMVar_hsa_circ_123323,RMVar_hsa_circ_206983,RMVar_hsa_circ_206984 26993 RMVar_ID_26993 Human_SNP_ID_113418431 A-to-I Human chr2 + 218573064 218573064 218573064 ATTCTGGGCCGGGCATGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGTGG ATTCTGGGCCGGGCATGGTGGCTCATGCCTGTGATCCCAGCACTTTGGGAGGCTGAGGCAGGTGG A G CNOT9 Ensembl:ENSG00000144580 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs760989450 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89564,RMVar_hsa_circ_123323,RMVar_hsa_circ_206983,RMVar_hsa_circ_206984 26994 RMVar_ID_26994 Human_SNP_ID_113418459 A-to-I Human chr2 + 218573197 218573197 218573197 AAAATTAGCCTGGCGTCATGGCATGCGCTTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGACA AAAATTAGCCTGGCGTCATGGCATGCGCTTGTGATCCCAGCTACTTGGGAGGCTGAGGCAGGACA A G CNOT9 Ensembl:ENSG00000144580 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs972200459 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17570186 RMVar_hsa_circ_89564,RMVar_hsa_circ_123323,RMVar_hsa_circ_206983,RMVar_hsa_circ_206984 26995 RMVar_ID_26995 Human_SNP_ID_113418674 A-to-I Human chr2 + 218574025 218574025 218574025 AGGATCTCGCTTTGTTACCCAGGCTGGAGTGCAGTGGTGTGATCTTGGCTCACCGCAACCTCGAC AGGATCTCGCTTTGTTACCCAGGCTGGAGTGCGGTGGTGTGATCTTGGCTCACCGCAACCTCGAC A G CNOT9 Ensembl:ENSG00000144580 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1212143186 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_359252,Human_Splice_Rec_359280 RMVar_hsa_circ_89564,RMVar_hsa_circ_123323,RMVar_hsa_circ_206983,RMVar_hsa_circ_206984 26996 RMVar_ID_26996 Human_SNP_ID_113418694 A-to-I Human chr2 + 218574069 218574069 218574069 TTGGCTCACCGCAACCTCGACCTTCTGGGTTCAGTCGATTCTCCCACCTCAGCCTCTTGAGTAGC TTGGCTCACCGCAACCTCGACCTTCTGGGTTCGGTCGATTCTCCCACCTCAGCCTCTTGAGTAGC A G CNOT9 Ensembl:ENSG00000144580 Protein coding intron GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831 ASD brains,frontal_cortex;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line - 30559470,31158229,32596459 RNA-Seq:(High) rs1299645406 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_359252,Human_Splice_Rec_359280 RMVar_hsa_circ_89564,RMVar_hsa_circ_123323,RMVar_hsa_circ_206983,RMVar_hsa_circ_206984 26997 RMVar_ID_26997 Human_SNP_ID_113418749 A-to-I Human chr2 + 218574199 218574199 218574199 ACTGTGTTGAAACTCCTGACCTCAAGTGATCCACCAGCCTCAGCCTCCCAAAGTGCTGGGATTAC ACTGTGTTGAAACTCCTGACCTCAAGTGATCCGCCAGCCTCAGCCTCCCAAAGTGCTGGGATTAC A G CNOT9 Ensembl:ENSG00000144580 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1420202685 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_359253 RMVar_hsa_circ_89564,RMVar_hsa_circ_123323,RMVar_hsa_circ_206983,RMVar_hsa_circ_206984 26998 RMVar_ID_26998 Human_SNP_ID_113419069 A-to-I Human chr2 + 218575568 218575568 218575568 GGGACTACAGGTGCCTGCCACCACACCTGGCTAATTTTTTTGTAGTTTTAGTAGAGATGGGATTT GGGACTACAGGTGCCTGCCACCACACCTGGCTGATTTTTTTGTAGTTTTAGTAGAGATGGGATTT A G CNOT9 Ensembl:ENSG00000144580 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs146364919 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89564,RMVar_hsa_circ_123323,RMVar_hsa_circ_206983,RMVar_hsa_circ_206984 26999 RMVar_ID_26999 Human_SNP_ID_113420487 A-to-I Human chr2 + 218581352 218581352 218581352 CACCATGCCTGGCTTTTTTTTTTTTAATTTTTAGTAGATACGGAGTTTCACCATGTTGGTCAGGC CACCATGCCTGGCTTTTTTTTTTTTAATTTTTGGTAGATACGGAGTTTCACCATGTTGGTCAGGC A G CNOT9 Ensembl:ENSG00000144580 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1278257630 Functional Loss SNV dbSNP153 33..33 33 - - - 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_301127,RMVar_hsa_circ_93825,RMVar_hsa_circ_289426,RMVar_hsa_circ_206986,RMVar_hsa_circ_206987,RMVar_hsa_circ_206985 27000 RMVar_ID_27000 Human_SNP_ID_113420495 A-to-I Human chr2 + 218581372 218581372 218581372 TTTTTAATTTTTAGTAGATACGGAGTTTCACCATGTTGGTCAGGCTGATCTTGAACTCCTGACCT TTTTTAATTTTTAGTAGATACGGAGTTTCACCCTGTTGGTCAGGCTGATCTTGAACTCCTGACCT A C CNOT9 Ensembl:ENSG00000144580 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs923875005 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17570187 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_301127,RMVar_hsa_circ_93825,RMVar_hsa_circ_289426,RMVar_hsa_circ_206986,RMVar_hsa_circ_206987,RMVar_hsa_circ_206985 27001 RMVar_ID_27001 Human_SNP_ID_113420496 A-to-I Human chr2 + 218581372 218581372 218581372 TTTTTAATTTTTAGTAGATACGGAGTTTCACCATGTTGGTCAGGCTGATCTTGAACTCCTGACCT TTTTTAATTTTTAGTAGATACGGAGTTTCACCGTGTTGGTCAGGCTGATCTTGAACTCCTGACCT A G CNOT9 Ensembl:ENSG00000144580 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs923875005 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17570187 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_301127,RMVar_hsa_circ_93825,RMVar_hsa_circ_289426,RMVar_hsa_circ_206986,RMVar_hsa_circ_206987,RMVar_hsa_circ_206985 27002 RMVar_ID_27002 Human_SNP_ID_113430613 A-to-I Human chr2 + 218620385 218620385 218620385 AAAATTAGCTGGGCGTGGCGACATGTATCTGCAATCCCAGCTACTCAGGAGGCTGAGGCACGAGA AAAATTAGCTGGGCGTGGCGACATGTATCTGCCATCCCAGCTACTCAGGAGGCTGAGGCACGAGA A C PLCD4 Ensembl:ENSG00000115556 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474135654 Functional Loss SNV dbSNP153 33..33 33 - - - 27003 RMVar_ID_27003 Human_SNP_ID_113434225 A-to-I Human chr2 - 218635018 218635018 218635018 TTCAGACTGGTCTCAAACTCCTGGGCTCAAGCAGTCCTCCTGCCTTGGCCTCCAAAGCGCTGGGA TTCAGACTGGTCTCAAACTCCTGGGCTCAAGCGGTCCTCCTGCCTTGGCCTCCAAAGCGCTGGGA T C lnc-ZNF142-5 RNACentral:URS0000D6DC48 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1377849569 Functional Loss SNV dbSNP153 33..33 33 - - - 27004 RMVar_ID_27004 Human_SNP_ID_113434263 A-to-I Human chr2 + 218635161 218635161 218635161 TGGCACATGACTATAGATAGTCCTGGCTACTCAGGAGGCTAAGGCTGGAGGGTCACTTTAGCCCA TGGCACATGACTATAGATAGTCCTGGCTACTCCGGAGGCTAAGGCTGGAGGGTCACTTTAGCCCA A C PLCD4 Ensembl:ENSG00000115556 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1410057767 Functional Loss SNV dbSNP153 33..33 33 - - - 27005 RMVar_ID_27005 Human_SNP_ID_113434264 A-to-I Human chr2 + 218635161 218635161 218635161 TGGCACATGACTATAGATAGTCCTGGCTACTCAGGAGGCTAAGGCTGGAGGGTCACTTTAGCCCA TGGCACATGACTATAGATAGTCCTGGCTACTCGGGAGGCTAAGGCTGGAGGGTCACTTTAGCCCA A G PLCD4 Ensembl:ENSG00000115556 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1410057767 Functional Loss SNV dbSNP153 33..33 33 - - - 27006 RMVar_ID_27006 Human_SNP_ID_113434283 A-to-I Human chr2 - 218635252 218635252 218635252 CCACTTTTTTTTTTTCAAAGAGACACGATCATACTCTTGACCAAGCTGGAATGCAGTGGGGCAGT CCACTTTTTTTTTTTCAAAGAGACACGATCATTCTCTTGACCAAGCTGGAATGCAGTGGGGCAGT T A lnc-ZNF142-5 RNACentral:URS0000D6DC48 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs371880210 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18314797 27007 RMVar_ID_27007 Human_SNP_ID_113434285 A-to-I Human chr2 - 218635257 218635257 218635257 AGCAGCCACTTTTTTTTTTTCAAAGAGACACGATCATACTCTTGACCAAGCTGGAATGCAGTGGG AGCAGCCACTTTTTTTTTTTCAAAGAGACACGGTCATACTCTTGACCAAGCTGGAATGCAGTGGG T C lnc-ZNF142-5 RNACentral:URS0000D6DC48 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1195147738 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18314797 27008 RMVar_ID_27008 Human_SNP_ID_113434315 A-to-I Human chr2 - 218635431 218635431 218635431 GGAAGGCTCAGATGGGAGAATCACTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCCAAGATCATG GGAAGGCTCAGATGGGAGAATCACTTGAACCCGGGAGGCGGAGGTTGCAGTGAGCCAAGATCATG T C lnc-ZNF142-5 RNACentral:URS0000D6DC48 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910895325 Functional Loss SNV dbSNP153 33..33 33 - - - 27009 RMVar_ID_27009 Human_SNP_ID_113439331 A-to-I Human chr2 - 218652365 218652365 218652365 ATTAAAAGATTCACCTACATTTTCTACTAGTAACTAACTCCTATGAGTCTTGTTCCATCTGATTC ATTAAAAGATTCACCTACATTTTCTACTAGTATCTAACTCCTATGAGTCTTGTTCCATCTGATTC T A ZNF142 Ensembl:ENSG00000115568 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4674323 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108325,RMVar_hsa_circ_87582,RMVar_hsa_circ_206999,RMVar_hsa_circ_116211,RMVar_hsa_circ_207001,RMVar_hsa_circ_207003,RMVar_hsa_circ_207005,RMVar_hsa_circ_374083,RMVar_hsa_circ_26259 27010 RMVar_ID_27010 Human_SNP_ID_113439332 A-to-I Human chr2 - 218652365 218652365 218652365 ATTAAAAGATTCACCTACATTTTCTACTAGTAACTAACTCCTATGAGTCTTGTTCCATCTGATTC ATTAAAAGATTCACCTACATTTTCTACTAGTAGCTAACTCCTATGAGTCTTGTTCCATCTGATTC T C ZNF142 Ensembl:ENSG00000115568 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4674323 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108325,RMVar_hsa_circ_87582,RMVar_hsa_circ_206999,RMVar_hsa_circ_116211,RMVar_hsa_circ_207001,RMVar_hsa_circ_207003,RMVar_hsa_circ_207005,RMVar_hsa_circ_374083,RMVar_hsa_circ_26259 27011 RMVar_ID_27011 Human_SNP_ID_113439473 A-to-I Human chr2 - 218653029 218653029 218653029 TGATCCTCCTGTCTCAGCCTCCCAAAGTGCCAAGATTACAGGCGTGAGCCACTGCACCTGGCCCT TGATCCTCCTGTCTCAGCCTCCCAAAGTGCCAGGATTACAGGCGTGAGCCACTGCACCTGGCCCT T C ZNF142 Ensembl:ENSG00000115568 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1435052019 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13775396 RMVar_hsa_circ_108325,RMVar_hsa_circ_87582,RMVar_hsa_circ_206999,RMVar_hsa_circ_116211,RMVar_hsa_circ_207001,RMVar_hsa_circ_207003,RMVar_hsa_circ_207005,RMVar_hsa_circ_374083,RMVar_hsa_circ_26259 27012 RMVar_ID_27012 Human_SNP_ID_113439474 A-to-I Human chr2 - 218653030 218653030 218653030 ATGATCCTCCTGTCTCAGCCTCCCAAAGTGCCAAGATTACAGGCGTGAGCCACTGCACCTGGCCC ATGATCCTCCTGTCTCAGCCTCCCAAAGTGCCGAGATTACAGGCGTGAGCCACTGCACCTGGCCC T C ZNF142 Ensembl:ENSG00000115568 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1368848729 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13775397,Human_RBP_ID_25514968 RMVar_hsa_circ_108325,RMVar_hsa_circ_87582,RMVar_hsa_circ_206999,RMVar_hsa_circ_116211,RMVar_hsa_circ_207001,RMVar_hsa_circ_207003,RMVar_hsa_circ_207005,RMVar_hsa_circ_374083,RMVar_hsa_circ_26259 27013 RMVar_ID_27013 Human_SNP_ID_113439695 A-to-I Human chr2 - 218653913 218653913 218653913 AGCAGGTCAAGGCTGCAGTGAGCTGTGATCACACCACCACTGCACTGCAGCCTGGGTGACAGAGA AGCAGGTCAAGGCTGCAGTGAGCTGTGATCACGCCACCACTGCACTGCAGCCTGGGTGACAGAGA T C ZNF142 Ensembl:ENSG00000115568 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1247894419 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25514979 RMVar_hsa_circ_108325,RMVar_hsa_circ_87582,RMVar_hsa_circ_206999,RMVar_hsa_circ_116211,RMVar_hsa_circ_207001,RMVar_hsa_circ_207003,RMVar_hsa_circ_207005,RMVar_hsa_circ_374083,RMVar_hsa_circ_26259 27014 RMVar_ID_27014 Human_SNP_ID_113439697 A-to-I Human chr2 - 218653945 218653945 218653945 AGGAGGCTGAGGTGGGAGAATCACTTGAGCCCAGCAGGTCAAGGCTGCAGTGAGCTGTGATCACA AGGAGGCTGAGGTGGGAGAATCACTTGAGCCCGGCAGGTCAAGGCTGCAGTGAGCTGTGATCACA T C ZNF142 Ensembl:ENSG00000115568 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1490065941 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108325,RMVar_hsa_circ_87582,RMVar_hsa_circ_206999,RMVar_hsa_circ_116211,RMVar_hsa_circ_207001,RMVar_hsa_circ_207003,RMVar_hsa_circ_207005,RMVar_hsa_circ_374083,RMVar_hsa_circ_26259 27015 RMVar_ID_27015 Human_SNP_ID_113439715 A-to-I Human chr2 - 218654037 218654037 218654037 TATTTTTAGAATGGGCAACATAGGGAGACCCCATCTCTACAAAAAAATTTAAAATTAGCCAGGAA TATTTTTAGAATGGGCAACATAGGGAGACCCCGTCTCTACAAAAAAATTTAAAATTAGCCAGGAA T C ZNF142 Ensembl:ENSG00000115568 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1352738238 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13775404,Human_RBP_ID_22989650 RMVar_hsa_circ_108325,RMVar_hsa_circ_87582,RMVar_hsa_circ_206999,RMVar_hsa_circ_116211,RMVar_hsa_circ_207001,RMVar_hsa_circ_207003,RMVar_hsa_circ_207005,RMVar_hsa_circ_374083,RMVar_hsa_circ_26259 27016 RMVar_ID_27016 Human_SNP_ID_113439807 A-to-I Human chr2 - 218654434 218654434 218654434 TGAACCCGAGAGGCGGAGGTTGCAGTGAGCCAAGATCGCACCACTGAACCCTAGCCTGGACAACA TGAACCCGAGAGGCGGAGGTTGCAGTGAGCCAGGATCGCACCACTGAACCCTAGCCTGGACAACA T C ZNF142 Ensembl:ENSG00000115568 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264426796 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108325,RMVar_hsa_circ_87582,RMVar_hsa_circ_206999,RMVar_hsa_circ_116211,RMVar_hsa_circ_207001,RMVar_hsa_circ_207003,RMVar_hsa_circ_207005,RMVar_hsa_circ_374083,RMVar_hsa_circ_26259 27017 RMVar_ID_27017 Human_SNP_ID_113439850 A-to-I Human chr2 - 218654640 218654640 218654640 AGAGATGTGGCTGGGCATGGTGGCTCATGCCTATAATCCTAGCACTTTGGGAGGCCGAGACAGGC AGAGATGTGGCTGGGCATGGTGGCTCATGCCTGTAATCCTAGCACTTTGGGAGGCCGAGACAGGC T C ZNF142 Ensembl:ENSG00000115568 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs560916894 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108325,RMVar_hsa_circ_87582,RMVar_hsa_circ_206999,RMVar_hsa_circ_116211,RMVar_hsa_circ_207001,RMVar_hsa_circ_207003,RMVar_hsa_circ_207005,RMVar_hsa_circ_374083,RMVar_hsa_circ_26259 27018 RMVar_ID_27018 Human_SNP_ID_113439903 A-to-I Human chr2 - 218654840 218654840 218654840 GCTCAAGCAATCTTCCCACCTCGGCCTCCTAAAGTTTTGGGATTACAGACATGAGCCATCGCACC GCTCAAGCAATCTTCCCACCTCGGCCTCCTAAGGTTTTGGGATTACAGACATGAGCCATCGCACC T C ZNF142 Ensembl:ENSG00000115568 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350445585 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108325,RMVar_hsa_circ_87582,RMVar_hsa_circ_206999,RMVar_hsa_circ_116211,RMVar_hsa_circ_207001,RMVar_hsa_circ_207003,RMVar_hsa_circ_207005,RMVar_hsa_circ_374083,RMVar_hsa_circ_26259 27019 RMVar_ID_27019 Human_SNP_ID_113439917 A-to-I Human chr2 - 218654888 218654888 218654888 TAGAAACGAGGTCTCACCTTGTTGCCCAGGCTAGTCTTGAACTCCTGGGCTCAAGCAATCTTCCC TAGAAACGAGGTCTCACCTTGTTGCCCAGGCTGGTCTTGAACTCCTGGGCTCAAGCAATCTTCCC T C ZNF142 Ensembl:ENSG00000115568 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1304887261 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13775427 RMVar_hsa_circ_108325,RMVar_hsa_circ_87582,RMVar_hsa_circ_206999,RMVar_hsa_circ_116211,RMVar_hsa_circ_207001,RMVar_hsa_circ_207003,RMVar_hsa_circ_207005,RMVar_hsa_circ_374083,RMVar_hsa_circ_26259 27020 RMVar_ID_27020 Human_SNP_ID_113439919 A-to-I Human chr2 - 218654893 218654893 218654893 TTTGGTAGAAACGAGGTCTCACCTTGTTGCCCAGGCTAGTCTTGAACTCCTGGGCTCAAGCAATC TTTGGTAGAAACGAGGTCTCACCTTGTTGCCCGGGCTAGTCTTGAACTCCTGGGCTCAAGCAATC T C ZNF142 Ensembl:ENSG00000115568 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1165177569 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13775427 RMVar_hsa_circ_108325,RMVar_hsa_circ_87582,RMVar_hsa_circ_206999,RMVar_hsa_circ_116211,RMVar_hsa_circ_207001,RMVar_hsa_circ_207003,RMVar_hsa_circ_207005,RMVar_hsa_circ_374083,RMVar_hsa_circ_26259 27021 RMVar_ID_27021 Human_SNP_ID_113439922 A-to-I Human chr2 - 218654915 218654915 218654915 CTCAGCTAGTTTTTAAATTTTCTTTGGTAGAAACGAGGTCTCACCTTGTTGCCCAGGCTAGTCTT CTCAGCTAGTTTTTAAATTTTCTTTGGTAGAATCGAGGTCTCACCTTGTTGCCCAGGCTAGTCTT T A ZNF142 Ensembl:ENSG00000115568 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs988699187 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13775428 RMVar_hsa_circ_108325,RMVar_hsa_circ_87582,RMVar_hsa_circ_206999,RMVar_hsa_circ_116211,RMVar_hsa_circ_207001,RMVar_hsa_circ_207003,RMVar_hsa_circ_207005,RMVar_hsa_circ_374083,RMVar_hsa_circ_26259 27022 RMVar_ID_27022 Human_SNP_ID_113439941 A-to-I Human chr2 - 218655002 218655002 218655002 TCACTGCAGCCTTGACCTCCTGGGCTTAAGCAATCCTCTTGCCTCAGCTTCCCATGTAGCTGGGG TCACTGCAGCCTTGACCTCCTGGGCTTAAGCAGTCCTCTTGCCTCAGCTTCCCATGTAGCTGGGG T C ZNF142 Ensembl:ENSG00000115568 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1271756075 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108325,RMVar_hsa_circ_87582,RMVar_hsa_circ_206999,RMVar_hsa_circ_116211,RMVar_hsa_circ_207001,RMVar_hsa_circ_207003,RMVar_hsa_circ_207005,RMVar_hsa_circ_374083,RMVar_hsa_circ_26259 27023 RMVar_ID_27023 Human_SNP_ID_113439953 A-to-I Human chr2 - 218655058 218655058 218655058 TTGAGACAGGGTCTTGCTCTGCCACCCAGGCTAGAGTGCAGTGGCACAGTTACGGCTCACTGCAG TTGAGACAGGGTCTTGCTCTGCCACCCAGGCTGGAGTGCAGTGGCACAGTTACGGCTCACTGCAG T C ZNF142 Ensembl:ENSG00000115568 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1270551197 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13775429 RMVar_hsa_circ_108325,RMVar_hsa_circ_87582,RMVar_hsa_circ_206999,RMVar_hsa_circ_116211,RMVar_hsa_circ_207001,RMVar_hsa_circ_207003,RMVar_hsa_circ_207005,RMVar_hsa_circ_374083,RMVar_hsa_circ_26259 27024 RMVar_ID_27024 Human_SNP_ID_113440079 A-to-I Human chr2 - 218655628 218655628 218655628 AGTTGAGGCCTGGTACAGTGGCATGCACCTGTAGTCTCAGCTACTTGGGAGGCTGAGGCAGGAAG AGTTGAGGCCTGGTACAGTGGCATGCACCTGTTGTCTCAGCTACTTGGGAGGCTGAGGCAGGAAG T A ZNF142 Ensembl:ENSG00000115568 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1250857037 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13775439,Human_RBP_ID_25514987 RMVar_hsa_circ_108325,RMVar_hsa_circ_87582,RMVar_hsa_circ_206999,RMVar_hsa_circ_116211,RMVar_hsa_circ_207001,RMVar_hsa_circ_207003,RMVar_hsa_circ_207005,RMVar_hsa_circ_374083,RMVar_hsa_circ_26259 27025 RMVar_ID_27025 Human_SNP_ID_113462403 A-to-I Human chr2 + 218742173 218742173 218742173 TTTTGTAGAGTTGTGGGGGAAGGTCTCATTATATTACCCAGGCTTGTCTTGAACTCTGGCCTCAA TTTTGTAGAGTTGTGGGGGAAGGTCTCATTATGTTACCCAGGCTTGTCTTGAACTCTGGCCTCAA A G TTLL4 Ensembl:ENSG00000135912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1370214974 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13776066,Human_RBP_ID_17570190 RMVar_hsa_circ_57527,RMVar_hsa_circ_8390,RMVar_hsa_circ_119251,RMVar_hsa_circ_28390,RMVar_hsa_circ_207033,RMVar_hsa_circ_91961,RMVar_hsa_circ_207034 27026 RMVar_ID_27026 Human_SNP_ID_113462406 A-to-I Human chr2 + 218742208 218742208 218742208 ACCCAGGCTTGTCTTGAACTCTGGCCTCAAGTAATCCTCTTGCTTTAGCCTCCCAAAGCACTGAG ACCCAGGCTTGTCTTGAACTCTGGCCTCAAGTGATCCTCTTGCTTTAGCCTCCCAAAGCACTGAG A G TTLL4 Ensembl:ENSG00000135912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs7595901 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17570190 RMVar_hsa_circ_57527,RMVar_hsa_circ_8390,RMVar_hsa_circ_119251,RMVar_hsa_circ_28390,RMVar_hsa_circ_207033,RMVar_hsa_circ_91961,RMVar_hsa_circ_207034 27027 RMVar_ID_27027 Human_SNP_ID_113474803 A-to-I Human chr2 + 218793853 218793853 218793853 CTCATGCCTCAGACTCCCAAGTAGCTGGGATTATAGGTATGCGCCACCATGCTTGGCTAATTTTT CTCATGCCTCAGACTCCCAAGTAGCTGGGATTGTAGGTATGCGCCACCATGCTTGGCTAATTTTT A G CYP27A1 Ensembl:ENSG00000135929 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285804479 Functional Loss SNV dbSNP153 33..33 33 - - - 27028 RMVar_ID_27028 Human_SNP_ID_113565980 A-to-I Human chr2 - 219157596 219157596 219157596 TCTCCTTCGCCCATTGTTGAAGGACGCTGCTCACCCTAGCGAAGCTACCTTCTCCTGTGATTGTG TCTCCTTCGCCCATTGTTGAAGGACGCTGCTCGCCCTAGCGAAGCTACCTTCTCCTGTGATTGTG T C AC068946.1,NHEJ1 Ensembl:ENSG00000280537,Ensembl:ENSG00000187736 Protein coding,Protein coding exon,CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1056296 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9385513 Human_Splice_Rec_360890,Human_Splice_Rec_360904,Human_Splice_Rec_360918,Human_Splice_Rec_360964,Human_Splice_Rec_361000,Human_Splice_Rec_361034 RMVar_hsa_circ_11917,RMVar_hsa_circ_49776,RMVar_hsa_circ_51823,RMVar_hsa_circ_207048,RMVar_hsa_circ_338853,RMVar_hsa_circ_122918,RMVar_hsa_circ_207049 27029 RMVar_ID_27029 Human_SNP_ID_113587697 A-to-I Human chr2 - 219226327 219226327 219226327 TGAAAAGAACCCAAGCCTTGGTTGGGCACGGCAGCTCACACCTGTAATCCCAGCACTTTAGGAGG TGAAAAGAACCCAAGCCTTGGTTGGGCACGGCGGCTCACACCTGTAATCCCAGCACTTTAGGAGG T C ATG9A Ensembl:ENSG00000198925 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1234955989 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126248,RMVar_hsa_circ_207087 27030 RMVar_ID_27030 Human_SNP_ID_113628514 A-to-I Human chr2 - 219371947 219371947 219371947 AACTATAGTGACAGCAGACCAGTGGTTGCTTGAATGTCAAGGATTGAGAGAGAGTTTGGTTGCAA AACTATAGTGACAGCAGACCAGTGGTTGCTTGGATGTCAAGGATTGAGAGAGAGTTTGGTTGCAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946202829 Functional Loss SNV dbSNP153 33..33 33 - - - 27031 RMVar_ID_27031 Human_SNP_ID_113628519 A-to-I Human chr2 - 219371975 219371975 219371975 TGGGATAAATTCTAGAAAATGCCAGCTGAACTATAGTGACAGCAGACCAGTGGTTGCTTGAATGT TGGGATAAATTCTAGAAAATGCCAGCTGAACTGTAGTGACAGCAGACCAGTGGTTGCTTGAATGT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs922341429 Functional Loss SNV dbSNP153 33..33 33 - - - 27032 RMVar_ID_27032 Human_SNP_ID_113683512 A-to-I Human chr2 - 219567290 219567290 219567290 CGGACATGGCCGTAGTCCCCACGTGGTGTTCCACGGTTCTGCTCACCTTGGTGAGTTGGTCCTGC CGGACATGGCCGTAGTCCCCACGTGGTGTTCCGCGGTTCTGCTCACCTTGGTGAGTTGGTCCTGC T C OBSL1 Ensembl:ENSG00000124006 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs374540973 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_921262,Human_RBP_ID_1911393,Human_RBP_ID_8845905,Human_RBP_ID_9295563,Human_RBP_ID_19000794,Human_RBP_ID_19102897,Human_RBP_ID_22450903 Human_Splice_Rec_364009,Human_Splice_Rec_364059,Human_Splice_Rec_364089,Human_Splice_Rec_364127,Human_Splice_Rec_364171,Human_Splice_Rec_364187 Human_miRNA_ID_2696764,Human_miRNA_ID_2696765 RMVar_hsa_circ_108853,RMVar_hsa_circ_86492,RMVar_hsa_circ_121295,RMVar_hsa_circ_207130,RMVar_hsa_circ_207134,RMVar_hsa_circ_207133,RMVar_hsa_circ_373329,RMVar_hsa_circ_207135,RMVar_hsa_circ_38649,RMVar_hsa_circ_207137,RMVar_hsa_circ_78133,RMVar_hsa_circ_327713,RMVar_hsa_circ_207136,RMVar_hsa_circ_307839,RMVar_hsa_circ_116258,RMVar_hsa_circ_207139,RMVar_hsa_circ_110435,RMVar_hsa_circ_207140,RMVar_hsa_circ_207141 27033 RMVar_ID_27033 Human_SNP_ID_113683521 A-to-I Human chr2 - 219567309 219567309 219567309 TCCGCATCTGCACAGTCAGCGGACATGGCCGTAGTCCCCACGTGGTGTTCCACGGTTCTGCTCAC TCCGCATCTGCACAGTCAGCGGACATGGCCGTGGTCCCCACGTGGTGTTCCACGGTTCTGCTCAC T C OBSL1 Ensembl:ENSG00000124006 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1419299067 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1022056,Human_RBP_ID_1911393,Human_RBP_ID_4597608,Human_RBP_ID_8845906 Human_Splice_Rec_364009,Human_Splice_Rec_364059,Human_Splice_Rec_364089,Human_Splice_Rec_364127,Human_Splice_Rec_364171,Human_Splice_Rec_364187 Human_miRNA_ID_2724919,Human_miRNA_ID_2724920 RMVar_hsa_circ_108853,RMVar_hsa_circ_86492,RMVar_hsa_circ_121295,RMVar_hsa_circ_207130,RMVar_hsa_circ_207134,RMVar_hsa_circ_207133,RMVar_hsa_circ_373329,RMVar_hsa_circ_207135,RMVar_hsa_circ_38649,RMVar_hsa_circ_207137,RMVar_hsa_circ_78133,RMVar_hsa_circ_327713,RMVar_hsa_circ_207136,RMVar_hsa_circ_307839,RMVar_hsa_circ_116258,RMVar_hsa_circ_207139,RMVar_hsa_circ_110435,RMVar_hsa_circ_207140,RMVar_hsa_circ_207141 27034 RMVar_ID_27034 Human_SNP_ID_113692552 A-to-I Human chr2 - 219599213 219599213 219599213 ATGGTGGTGCACACCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTCGTCCCA ATGGTGGTGCACACCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTCGTCCCA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1430228147 Functional Loss SNV dbSNP153 33..33 33 - - - 27035 RMVar_ID_27035 Human_SNP_ID_113848489 A-to-I Human chr2 + 220234438 220234438 220234438 AAAATTAGCTGGGTGTGGTGGCACGTGCTGGTAGTCCCAGCTACTCAGGAGGCCGAGGCACGAGA AAAATTAGCTGGGTGTGGTGGCACGTGCTGGTGGTCCCAGCTACTCAGGAGGCCGAGGCACGAGA A G AC019211.1 Ensembl:ENSG00000239498 lincRNA intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1353345972 Functional Loss SNV dbSNP153 33..33 33 - - - 27036 RMVar_ID_27036 Human_SNP_ID_114274773 A-to-I Human chr2 + 221962580 221962580 221962580 AGGTGGGGAAGACTTTGACCAGGCCTTGCTACAGCACATTGTGAAGGAGTTCAAGAGAGAGACGG AGGTGGGGAAGACTTTGACCAGGCCTTGCTACGGCACATTGTGAAGGAGTTCAAGAGAGAGACGG A G HSPA9P1 Ensembl:ENSG00000226666 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs558594963 Functional Loss SNV dbSNP153 33..33 33 - - - 27037 RMVar_ID_27037 Human_SNP_ID_114422094 A-to-I Human chr2 + 222559603 222559603 222559603 CCTGCCTGAGCCAACTGAGTAGCTGGGACTGTAAGCATAGACCACCATGTGCCCAGCTAATTTTT CCTGCCTGAGCCAACTGAGTAGCTGGGACTGTGAGCATAGACCACCATGTGCCCAGCTAATTTTT A G SGPP2 Ensembl:ENSG00000163082 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs957320623 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8512736 27038 RMVar_ID_27038 Human_SNP_ID_114423971 A-to-I Human chr2 - 222566729 222566729 222566729 TCCCTAATCTACCTGTATCCATGAGCGCAGATAGGAGTGAAGCCTCCTAGGCTTCCAGTCTGCAG TCCCTAATCTACCTGTATCCATGAGCGCAGATTGGAGTGAAGCCTCCTAGGCTTCCAGTCTGCAG T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1559183501 Functional Loss SNV dbSNP153 33..33 33 - - - 27039 RMVar_ID_27039 Human_SNP_ID_114497705 A-to-I Human chr2 + 222874299 222874299 222874299 CGTCTGCCTCGGTCTCCCAAGGTGCTGGGATTACAGGCGTGGGCCACTGTGCCCGGCCTTGTACT CGTCTGCCTCGGTCTCCCAAGGTGCTGGGATTGCAGGCGTGGGCCACTGTGCCCGGCCTTGTACT A G ACSL3 Ensembl:ENSG00000123983 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1415018130 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17570192 27040 RMVar_ID_27040 Human_SNP_ID_114497743 A-to-I Human chr2 + 222874433 222874433 222874433 AATTTCTTGGCTGGGCACAGTGGCTAACGTCTATAATCCCAGGACTTCGGGAGGCTGAGGAGGAA AATTTCTTGGCTGGGCACAGTGGCTAACGTCTGTAATCCCAGGACTTCGGGAGGCTGAGGAGGAA A G ACSL3 Ensembl:ENSG00000123983 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1207702569 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17570193 27041 RMVar_ID_27041 Human_SNP_ID_114713102 A-to-I Human chr2 - 223751664 223751664 223751664 AAAAAAAAAAACTATTGTAGACAAAGTGTCTCACTATGTTGCCCAGGCTGGTCTCAAACTTCTGG AAAAAAAAAAACTATTGTAGACAAAGTGTCTCGCTATGTTGCCCAGGCTGGTCTCAAACTTCTGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs764566495 Functional Loss SNV dbSNP153 33..33 33 - - - 27042 RMVar_ID_27042 Human_SNP_ID_114713141 A-to-I Human chr2 - 223751808 223751808 223751808 ATCTCACTCTGTCACCCAGGCTGGAGTGCAGTAGCACGATAGCAGCGCACTGCAACCTGGACCTC ATCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGCACGATAGCAGCGCACTGCAACCTGGACCTC T C AP1S3 Ensembl:ENSG00000152056 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1281635195 Functional Loss SNV dbSNP153 33..33 33 - - - 27043 RMVar_ID_27043 Human_SNP_ID_114713419 A-to-I Human chr2 - 223752845 223752845 223752845 CCCAGAGGCAGAGATTGCAGTGAGCCGAGATCATGCCATTGCACTCTAGCCTAGGCAACAAGAGC CCCAGAGGCAGAGATTGCAGTGAGCCGAGATCGTGCCATTGCACTCTAGCCTAGGCAACAAGAGC T C AP1S3 Ensembl:ENSG00000152056 Protein coding CDS GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs555805533 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_365228 27044 RMVar_ID_27044 Human_SNP_ID_114713718 A-to-I Human chr2 - 223753994 223753994 223753994 GGCTCAAGCGATCCTCCCACCTTGGCCTCCCAAAGTATTGGGACTACAGGCATAAGCCACCATGC GGCTCAAGCGATCCTCCCACCTTGGCCTCCCACAGTATTGGGACTACAGGCATAAGCCACCATGC T G AP1S3 Ensembl:ENSG00000152056 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1424182100 Functional Loss SNV dbSNP153 33..33 33 - - - 27045 RMVar_ID_27045 Human_SNP_ID_114713724 A-to-I Human chr2 - 223754033 223754033 223754033 GCGTTCTCCCTGAGTTCCCAGGCTGATCTCGAACTCCTGGGCTCAAGCGATCCTCCCACCTTGGC GCGTTCTCCCTGAGTTCCCAGGCTGATCTCGAGCTCCTGGGCTCAAGCGATCCTCCCACCTTGGC T C AP1S3 Ensembl:ENSG00000152056 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs868430712 Functional Loss SNV dbSNP153 33..33 33 - - - 27046 RMVar_ID_27046 Human_SNP_ID_114713754 A-to-I Human chr2 - 223754127 223754127 223754127 CTCACCACAGCCTCCCAAATAGCTGAGACTACAGGAATGCACTGCCATGCCTGGCTAATTTTTAA CTCACCACAGCCTCCCAAATAGCTGAGACTACGGGAATGCACTGCCATGCCTGGCTAATTTTTAA T C AP1S3 Ensembl:ENSG00000152056 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs770149904 Functional Loss SNV dbSNP153 33..33 33 - - - 27047 RMVar_ID_27047 Human_SNP_ID_114713756 A-to-I Human chr2 - 223754143 223754143 223754143 GGTCTTAAGGGATCCTCTCACCACAGCCTCCCAAATAGCTGAGACTACAGGAATGCACTGCCATG GGTCTTAAGGGATCCTCTCACCACAGCCTCCCGAATAGCTGAGACTACAGGAATGCACTGCCATG T C AP1S3 Ensembl:ENSG00000152056 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs142787380 Functional Loss SNV dbSNP153 33..33 33 - - - 27048 RMVar_ID_27048 Human_SNP_ID_114713903 A-to-I Human chr2 - 223754761 223754761 223754761 GGGATTACAGGTATGCGCCACGTGCCTGGCTAATTTTTGTGTTTTTGGTAGAGACGGGGTTTCAC GGGATTACAGGTATGCGCCACGTGCCTGGCTACTTTTTGTGTTTTTGGTAGAGACGGGGTTTCAC T G AP1S3 Ensembl:ENSG00000152056 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs963450423 Functional Loss SNV dbSNP153 33..33 33 - - - 27049 RMVar_ID_27049 Human_SNP_ID_114714115 A-to-I Human chr2 - 223755659 223755659 223755659 AAGTGTGGTGGCACATGCTTGTAGTGCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAA AAGTGTGGTGGCACATGCTTGTAGTGCCAGCTGCTCAGGAGGCTGAGGCAGGAGAATCGCTTGAA T C AP1S3 Ensembl:ENSG00000152056 Protein coding intron GSE38233;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;Bronchiolar epithelium,BERP35T4 cell line - 24183664,31158229 RNA-Seq:(High) rs1460215694 Functional Loss SNV dbSNP153 33..33 33 - - - 27050 RMVar_ID_27050 Human_SNP_ID_114714121 A-to-I Human chr2 - 223755679 223755679 223755679 TAAAAATTCAAAAATTAGCCAAGTGTGGTGGCACATGCTTGTAGTGCCAGCTACTCAGGAGGCTG TAAAAATTCAAAAATTAGCCAAGTGTGGTGGCTCATGCTTGTAGTGCCAGCTACTCAGGAGGCTG T A AP1S3 Ensembl:ENSG00000152056 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs12151747 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2773,GWAS_ID_2774,GWAS_ID_2775 27051 RMVar_ID_27051 Human_SNP_ID_114714122 A-to-I Human chr2 - 223755679 223755679 223755679 TAAAAATTCAAAAATTAGCCAAGTGTGGTGGCACATGCTTGTAGTGCCAGCTACTCAGGAGGCTG TAAAAATTCAAAAATTAGCCAAGTGTGGTGGCGCATGCTTGTAGTGCCAGCTACTCAGGAGGCTG T C AP1S3 Ensembl:ENSG00000152056 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs12151747 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2773,GWAS_ID_2774,GWAS_ID_2775 27052 RMVar_ID_27052 Human_SNP_ID_114714132 A-to-I Human chr2 - 223755706 223755706 223755706 GCCAACATGGTGAAACCCTGTCTCTACTAAAAATTCAAAAATTAGCCAAGTGTGGTGGCACATGC GCCAACATGGTGAAACCCTGTCTCTACTAAAAGTTCAAAAATTAGCCAAGTGTGGTGGCACATGC T C AP1S3 Ensembl:ENSG00000152056 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs987122832 Functional Loss SNV dbSNP153 33..33 33 - - - 27053 RMVar_ID_27053 Human_SNP_ID_114714133 A-to-I Human chr2 - 223755706 223755706 223755706 GCCAACATGGTGAAACCCTGTCTCTACTAAAAATTCAAAAATTAGCCAAGTGTGGTGGCACATGC GCCAACATGGTGAAACCCTGTCTCTACTAAAACTTCAAAAATTAGCCAAGTGTGGTGGCACATGC T G AP1S3 Ensembl:ENSG00000152056 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs987122832 Functional Loss SNV dbSNP153 33..33 33 - - - 27054 RMVar_ID_27054 Human_SNP_ID_114714223 A-to-I Human chr2 - 223756076 223756076 223756076 CCTTGGCCTTCCAAAGTGCTGGAATTACAGGCATGAGCCGCTGCACCCGGCCAAATTCTTTATTT CCTTGGCCTTCCAAAGTGCTGGAATTACAGGCGTGAGCCGCTGCACCCGGCCAAATTCTTTATTT T C AP1S3 Ensembl:ENSG00000152056 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1043761159 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23182291 27055 RMVar_ID_27055 Human_SNP_ID_114714248 A-to-I Human chr2 - 223756155 223756155 223756155 TTTTGTATTTTTGGTAGAGTTGGGATTTCTCCATGTTGGTCAGGCTGGTCTTGAACGCCGACCTC TTTTGTATTTTTGGTAGAGTTGGGATTTCTCCGTGTTGGTCAGGCTGGTCTTGAACGCCGACCTC T C AP1S3 Ensembl:ENSG00000152056 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs377247304 Functional Loss SNV dbSNP153 33..33 33 - - - 27056 RMVar_ID_27056 Human_SNP_ID_114714281 A-to-I Human chr2 - 223756254 223756254 223756254 CAGGTCACTGCAGCCTCCGTCTCCTGGGTTCAAACGATTCTCCTGCCTCAGCCTCCCGAGTAGCT CAGGTCACTGCAGCCTCCGTCTCCTGGGTTCAGACGATTCTCCTGCCTCAGCCTCCCGAGTAGCT T C AP1S3 Ensembl:ENSG00000152056 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs976554248 Functional Loss SNV dbSNP153 33..33 33 - - - 27057 RMVar_ID_27057 Human_SNP_ID_114714288 A-to-I Human chr2 - 223756290 223756290 223756290 TCTTGTCACCCAGGCCAGAGTGCAATGGTGTGATCTCAGGTCACTGCAGCCTCCGTCTCCTGGGT TCTTGTCACCCAGGCCAGAGTGCAATGGTGTGTTCTCAGGTCACTGCAGCCTCCGTCTCCTGGGT T A AP1S3 Ensembl:ENSG00000152056 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1167839401 Functional Loss SNV dbSNP153 33..33 33 - - - 27058 RMVar_ID_27058 Human_SNP_ID_114714533 A-to-I Human chr2 - 223757057 223757057 223757057 TGAACCCAGGAGGCAGAGGTTGCAGTGAGCCAAGGTCATACCAGTGCACTCCAGGCGGGTGACAG TGAACCCAGGAGGCAGAGGTTGCAGTGAGCCAGGGTCATACCAGTGCACTCCAGGCGGGTGACAG T C AP1S3 Ensembl:ENSG00000152056 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042637141 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13781638 Human_miRNA_ID_468663,Human_miRNA_ID_606815 27059 RMVar_ID_27059 Human_SNP_ID_114714535 A-to-I Human chr2 - 223757066 223757066 223757066 GGAATGGCTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCCAAGGTCATACCAGTGCACTCCAGGC GGAATGGCTTGAACCCAGGAGGCAGAGGTTGCGGTGAGCCAAGGTCATACCAGTGCACTCCAGGC T C AP1S3 Ensembl:ENSG00000152056 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1319451625 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13781638 Human_miRNA_ID_620418 27060 RMVar_ID_27060 Human_SNP_ID_114714542 A-to-I Human chr2 - 223757086 223757086 223757086 ACTCAGGGGGCTGAGGCAGGGGAATGGCTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCCAAGGT ACTCAGGGGGCTGAGGCAGGGGAATGGCTTGAGCCCAGGAGGCAGAGGTTGCAGTGAGCCAAGGT T C AP1S3 Ensembl:ENSG00000152056 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs751627365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_254627,Human_miRNA_ID_1462779 27061 RMVar_ID_27061 Human_SNP_ID_114714548 A-to-I Human chr2 - 223757114 223757112 223757114 ATGGTGGCAGGTGCCTGTAATCCCAGCTACTCAGGGGGCTGAGGCAGGGGAATGGCTTGAACCCA ATGGTGGCAGGTGCCTGTAATCCCAGCTACTC__GGGGCTGAGGCAGGGGAATGGCTTGAACCCA CCT C AP1S3 Ensembl:ENSG00000152056 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 31158229,32596459,32596459 RNA-Seq:(High) rs1365920567 Functional Loss DEL dbSNP153 33..34 33 - - - Human_miRNA_ID_120666,Human_miRNA_ID_124481,Human_miRNA_ID_960435 27062 RMVar_ID_27062 Human_SNP_ID_114714549 A-to-I Human chr2 - 223757114 223757114 223757114 ATGGTGGCAGGTGCCTGTAATCCCAGCTACTCAGGGGGCTGAGGCAGGGGAATGGCTTGAACCCA ATGGTGGCAGGTGCCTGTAATCCCAGCTACTCCGGGGGCTGAGGCAGGGGAATGGCTTGAACCCA T G AP1S3 Ensembl:ENSG00000152056 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 31158229,32596459,32596459 RNA-Seq:(High) rs965373162 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_120666,Human_miRNA_ID_124481,Human_miRNA_ID_960435 27063 RMVar_ID_27063 Human_SNP_ID_114718007 A-to-I Human chr2 - 223771323 223771323 223771323 TATTTTGTTTCTTTTTCCCGAGACAGAGTCTTACTCCGTTGCCCAGGTTGGGGTGCAGTGGTGCA TATTTTGTTTCTTTTTCCCGAGACAGAGTCTTGCTCCGTTGCCCAGGTTGGGGTGCAGTGGTGCA T C AP1S3,AC093884.1 Ensembl:ENSG00000152056,Ensembl:ENSG00000286239 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1046907334 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_207231,RMVar_hsa_circ_304271,RMVar_hsa_circ_37331 27064 RMVar_ID_27064 Human_SNP_ID_114719482 A-to-I Human chr2 - 223777735 223777735 223777735 GTTCAGATTATTCTCTCCCGTGGTCACAGGACAAGCAGTTTTGTTGACTGGAAGGAGCTAAAACT GTTCAGATTATTCTCTCCCGTGGTCACAGGACGAGCAGTTTTGTTGACTGGAAGGAGCTAAAACT T C AP1S3,AC093884.1 Ensembl:ENSG00000152056,Ensembl:ENSG00000286239 Protein coding,Protein coding CDS,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1454932351 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1911631,Human_RBP_ID_9103323,Human_RBP_ID_13781719 Human_Splice_Rec_365223,Human_Splice_Rec_365231,Human_Splice_Rec_365239,Human_Splice_Rec_365249,Human_Splice_Rec_365255,Human_Splice_Rec_365259,Human_Splice_Rec_365265,Human_Splice_Rec_365271,Human_Splice_Rec_365303 Human_miRNA_ID_2031506,Human_miRNA_ID_2254166,Human_miRNA_ID_2761248,Human_miRNA_ID_2886444 RMVar_hsa_circ_207231,RMVar_hsa_circ_304271,RMVar_hsa_circ_282482,RMVar_hsa_circ_37331,RMVar_hsa_circ_207232 27065 RMVar_ID_27065 Human_SNP_ID_114733379 A-to-I Human chr2 - 223834559 223834554 223834559 TTTGAGACAAGGCTTGTTCTATCACCCAGAGTAGAGTGCAGTAGCATGAACATGGCTTACTGCAG TTTGAGACAAGGCTTGTTCTATCACCCAGAGT_____GCAGTAGCATGAACATGGCTTACTGCAG CACTCT C AP1S3,AC093884.1 Ensembl:ENSG00000152056,Ensembl:ENSG00000286239 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1303649149 Functional Loss DEL dbSNP153 33..37 33 - - - Human_RBP_ID_23854848 27066 RMVar_ID_27066 Human_SNP_ID_114737622 A-to-I Human chr2 - 223853069 223853069 223853069 AACACTCCTGGCTAATTTTTGTATTTTTTGGTAGAGACAGGGTTTCACCATGTTGGGCTGGGCAG AACACTCCTGGCTAATTTTTGTATTTTTTGGTGGAGACAGGGTTTCACCATGTTGGGCTGGGCAG T C AC093884.1 Ensembl:ENSG00000286239 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334390981 Functional Loss SNV dbSNP153 33..33 33 - - - 27067 RMVar_ID_27067 Human_SNP_ID_114764861 A-to-I Human chr2 + 223963322 223963322 223963322 AAAGCTAGCCGAGTATGGTGGTGTGCACCTGTAGTCTCAGCTGCTGAAGAGGCTGAGCTAGGAGG AAAGCTAGCCGAGTATGGTGGTGTGCACCTGTGGTCTCAGCTGCTGAAGAGGCTGAGCTAGGAGG A G MRPL44 Ensembl:ENSG00000135900 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1227214207 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81622,RMVar_hsa_circ_207262 27068 RMVar_ID_27068 Human_SNP_ID_114898093 A-to-I Human chr2 - 224509282 224509282 224509282 TCTGGCTGGGGAGGTCAAGGCTGCAGTGAACCAAGATGATGCCACTGCACTCCAGCCTGGGCTAC TCTGGCTGGGGAGGTCAAGGCTGCAGTGAACCTAGATGATGCCACTGCACTCCAGCCTGGGCTAC T A CUL3 Ensembl:ENSG00000036257 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs935100064 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_296757,RMVar_hsa_circ_9930,RMVar_hsa_circ_104162,RMVar_hsa_circ_207272,RMVar_hsa_circ_15877,RMVar_hsa_circ_207274,RMVar_hsa_circ_207275,RMVar_hsa_circ_363017,RMVar_hsa_circ_281427,RMVar_hsa_circ_207279,RMVar_hsa_circ_207280,RMVar_hsa_circ_207281,RMVar_hsa_circ_370496,RMVar_hsa_circ_37243,RMVar_hsa_circ_64439,RMVar_hsa_circ_372038,RMVar_hsa_circ_286916,RMVar_hsa_circ_338843,RMVar_hsa_circ_207282 27069 RMVar_ID_27069 Human_SNP_ID_114898113 A-to-I Human chr2 - 224509399 224509399 224509399 CAACCTGGGCAAATTGGTGAAACCCTGTCTCTATGAAAAATACAAAAATTAGCTGGGCATGATGG CAACCTGGGCAAATTGGTGAAACCCTGTCTCTGTGAAAAATACAAAAATTAGCTGGGCATGATGG T C CUL3 Ensembl:ENSG00000036257 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1379113366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25517246 RMVar_hsa_circ_296757,RMVar_hsa_circ_9930,RMVar_hsa_circ_104162,RMVar_hsa_circ_207272,RMVar_hsa_circ_15877,RMVar_hsa_circ_207274,RMVar_hsa_circ_207275,RMVar_hsa_circ_363017,RMVar_hsa_circ_281427,RMVar_hsa_circ_207279,RMVar_hsa_circ_207280,RMVar_hsa_circ_207281,RMVar_hsa_circ_370496,RMVar_hsa_circ_37243,RMVar_hsa_circ_64439,RMVar_hsa_circ_372038,RMVar_hsa_circ_286916,RMVar_hsa_circ_338843,RMVar_hsa_circ_207282 27070 RMVar_ID_27070 Human_SNP_ID_114901304 A-to-I Human chr2 - 224521559 224521559 224521559 GGGCATGGTGGCACATACCTGTAATCCCAGCTACTAGCGGGGCTGAGGCAGGAGGATCACTTGAA GGGCATGGTGGCACATACCTGTAATCCCAGCTGCTAGCGGGGCTGAGGCAGGAGGATCACTTGAA T C CUL3 Ensembl:ENSG00000036257 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1273080427 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_296757,RMVar_hsa_circ_207274,RMVar_hsa_circ_363017,RMVar_hsa_circ_207280,RMVar_hsa_circ_207281,RMVar_hsa_circ_370496,RMVar_hsa_circ_37243,RMVar_hsa_circ_64439,RMVar_hsa_circ_372038,RMVar_hsa_circ_207282,RMVar_hsa_circ_349331,RMVar_hsa_circ_63605,RMVar_hsa_circ_52371 27071 RMVar_ID_27071 Human_SNP_ID_114903802 A-to-I Human chr2 - 224530750 224530750 224530750 GGTGCATGCCACCACACCTGGCTAATTTTTGTATTTTTGGTAGAGATGGGGTTTCGCCATGTTGG GGTGCATGCCACCACACCTGGCTAATTTTTGTGTTTTTGGTAGAGATGGGGTTTCGCCATGTTGG T C CUL3 Ensembl:ENSG00000036257 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs573199767 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25517380 RMVar_hsa_circ_296757,RMVar_hsa_circ_207274,RMVar_hsa_circ_363017,RMVar_hsa_circ_207280,RMVar_hsa_circ_207281,RMVar_hsa_circ_370496,RMVar_hsa_circ_37243,RMVar_hsa_circ_64439,RMVar_hsa_circ_372038,RMVar_hsa_circ_207282,RMVar_hsa_circ_349331,RMVar_hsa_circ_63605,RMVar_hsa_circ_52371,RMVar_hsa_circ_207285,RMVar_hsa_circ_207286 27072 RMVar_ID_27072 Human_SNP_ID_114916992 A-to-I Human chr2 - 224581247 224581247 224581247 GGGATTACAGGCGTGTGCCACCACGCCTGGCTAGTTTCTGTCTTTTTAGTAGAGATGGGGTTTCA GGGATTACAGGCGTGTGCCACCACGCCTGGCTGGTTTCTGTCTTTTTAGTAGAGATGGGGTTTCA T C CUL3 Ensembl:ENSG00000036257 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251967537 Functional Loss SNV dbSNP153 33..33 33 - - - 27073 RMVar_ID_27073 Human_SNP_ID_114917274 A-to-I Human chr2 - 224582129 224582129 224582129 AAATCCCATCTCTACTTAAAATACAAAAAATTAGCGGGGCGTGGTGGCGGATGCCTGTAAACCTA AAATCCCATCTCTACTTAAAATACAAAAAATTCGCGGGGCGTGGTGGCGGATGCCTGTAAACCTA T G CUL3 Ensembl:ENSG00000036257 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1384612538 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17570201,Human_RBP_ID_25517569 27074 RMVar_ID_27074 Human_SNP_ID_114973616 A-to-I Human chr2 - 224813433 224813433 224813433 TCAACACTTTGGGAGGCCGAGGCAGGCAGATCACTTGAGGCCAGGAGTTCGACATCACCCTGGCC TCAACACTTTGGGAGGCCGAGGCAGGCAGATCGCTTGAGGCCAGGAGTTCGACATCACCCTGGCC T C DOCK10 Ensembl:ENSG00000135905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1200594758 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266363,RMVar_hsa_circ_269753,RMVar_hsa_circ_67559,RMVar_hsa_circ_267329,RMVar_hsa_circ_113188,RMVar_hsa_circ_207292 27075 RMVar_ID_27075 Human_SNP_ID_114985265 A-to-I Human chr2 - 224864352 224864351 224864352 GTGCATGCCACCACGCCCAGCTAATTTTTTGTATTTTATAGTAGAGATGGGGTTTCACCATGTTG GTGCATGCCACCACGCCCAGCTAATTTTTTGT_TTTTATAGTAGAGATGGGGTTTCACCATGTTG AT A DOCK10 Ensembl:ENSG00000135905 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1359555466 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_266634,RMVar_hsa_circ_49937,RMVar_hsa_circ_85239,RMVar_hsa_circ_207299,RMVar_hsa_circ_19668,RMVar_hsa_circ_59172,RMVar_hsa_circ_66677,RMVar_hsa_circ_357900,RMVar_hsa_circ_4821,RMVar_hsa_circ_305694 27076 RMVar_ID_27076 Human_SNP_ID_114997828 A-to-I Human chr2 - 224916539 224916537 224916539 GTGGATGTCTTTTTTTTTTTTTTTTTTTTTTGAGGGAGGGTGTCACTCTGTCACCCAGGCTGGAG GTGGATGTCTTTTTTTTTTTTTTTTTTTTTTG__GGAGGGTGTCACTCTGTCACCCAGGCTGGAG CCT C DOCK10 Ensembl:ENSG00000135905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1559751758 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_49937,RMVar_hsa_circ_69828,RMVar_hsa_circ_353199 27077 RMVar_ID_27077 Human_SNP_ID_599399990 A-to-I Human chr16 - 30013852 30013852 30013852 ACTTAGCCAAGTGTGGGGCGTGCGCCCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAA ACTTAGCCAAGTGTGGGGCGTGCGCCCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAA T C DOC2A Ensembl:ENSG00000149927 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042203090 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 27078 RMVar_ID_27078 Human_SNP_ID_599414881 A-to-I Human chr16 + 30068492 30068489 30068493 CTAAAGAAGAGGAAAGAGGGGCACGCCCAGCTACCTAGGAGGCTGAGGCGGGAGGATCACTTGAG CTAAAGAAGAGGAAAGAGGGGCACGCCCAG____CTAGGAGGCTGAGGCGGGAGGATCACTTGAG GCTAC G ALDOA,AC093512.2 Ensembl:ENSG00000149925,Ensembl:ENSG00000285043 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973328473 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_5355763,Human_RBP_ID_22651928,Human_RBP_ID_26779230 RMVar_hsa_circ_105537,RMVar_hsa_circ_85201,RMVar_hsa_circ_80629,RMVar_hsa_circ_88608,RMVar_hsa_circ_177809,RMVar_hsa_circ_123478,RMVar_hsa_circ_177811,RMVar_hsa_circ_177813,RMVar_hsa_circ_102202,RMVar_hsa_circ_177812,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_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 27079 RMVar_ID_27079 Human_SNP_ID_599416282 A-to-I Human chr16 + 30072148 30072148 30072148 AATGGTGAGCCGAGATTGTGCCACTGCACTCCAGCCTAGGCAACAGAGCCAGACTCCGTCCCAAA AATGGTGAGCCGAGATTGTGCCACTGCACTCCCGCCTAGGCAACAGAGCCAGACTCCGTCCCAAA A C ALDOA Ensembl:ENSG00000149925 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1481264765 Functional Loss SNV dbSNP153 33..33 33 - - - 27080 RMVar_ID_27080 Human_SNP_ID_599417117 A-to-I Human chr16 + 30074795 30074795 30074795 AGGCGGAGCTTGCAGTGAGCCGAGATGGCGCCACTGGACTGCAGCCTGGGCGACAGAGCGAGAGA AGGCGGAGCTTGCAGTGAGCCGAGATGGCGCCGCTGGACTGCAGCCTGGGCGACAGAGCGAGAGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1321179399 Functional Loss SNV dbSNP153 33..33 33 - - - 27081 RMVar_ID_27081 Human_SNP_ID_599418813 A-to-I Human chr16 + 30080576 30080576 30080588 TCGCCCAGGCTGGAGTGCAGTGGCGCGATCTTAGCTCACTGCAGCCCCCACCTCCCAGGTTCAAG TCGCCCAGGCTGGAGTGCAGTGGCGCGATCTTTGCTCACTGCAAACCCCACCTCCCAGGTTCAAG AGCTCACTGCAGC TGCTCACTGCAAA PPP4C Ensembl:ENSG00000149923 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs71391266 Functional Loss MNV dbSNP153 33..45 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 27082 RMVar_ID_27082 Human_SNP_ID_599418874 A-to-I Human chr16 + 30080781 30080781 30080781 CCCACCCTGGCATCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCACCTGGCCAAGAGCGCA CCCACCCTGGCATCCCAAAGTGCTGGGATTACGGGCATGAGCCACCGCACCTGGCCAAGAGCGCA A G PPP4C Ensembl:ENSG00000149923 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs370973785 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 27083 RMVar_ID_27083 Human_SNP_ID_599454255 A-to-I Human chr16 - 30238551 30238551 30238551 CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCGCCCGCCACTACGCCCGGCTAATTTTT CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTGCAGGCGCCCGCCACTACGCCCGGCTAATTTTT T C NPIPB13 Ensembl:ENSG00000198064 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1221835214 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 27084 RMVar_ID_27084 Human_SNP_ID_599454604 A-to-I Human chr16 - 30244234 30244234 30244234 TGACCTCGTGATCTGCCCACCGCGGCCTCCCAAAGTGCTGGGACTTTAGGTGTGAGCCGCTGCAC TGACCTCGTGATCTGCCCACCGCGGCCTCCCATAGTGCTGGGACTTTAGGTGTGAGCCGCTGCAC T A NPIPB13 Ensembl:ENSG00000198064 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1457030723 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 27085 RMVar_ID_27085 Human_SNP_ID_599454605 A-to-I Human chr16 - 30244234 30244234 30244234 TGACCTCGTGATCTGCCCACCGCGGCCTCCCAAAGTGCTGGGACTTTAGGTGTGAGCCGCTGCAC TGACCTCGTGATCTGCCCACCGCGGCCTCCCACAGTGCTGGGACTTTAGGTGTGAGCCGCTGCAC T G NPIPB13 Ensembl:ENSG00000198064 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1457030723 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232 27086 RMVar_ID_27086 Human_SNP_ID_599459657 A-to-I Human chr16 - 30283262 30283244 30283263 CAGCCTGGGCTACAGAACCAGACTCTGTCTCAAAAGAAAAAAAAAAAAAAGAAAGAAAGAAACAA CAGCCTGGGCTACAGAACCAGACTCTGTCTC___________________GAAAGAAAGAAACAA CTTTTTTTTTTTTTTCTTTT C SMG1P5 Ensembl:ENSG00000183604 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1241622353 Functional Loss DEL dbSNP153 32..50 33 - - - RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232,RMVar_hsa_circ_70636,RMVar_hsa_circ_110297,RMVar_hsa_circ_177862,RMVar_hsa_circ_328446 27087 RMVar_ID_27087 Human_SNP_ID_599459676 A-to-I Human chr16 - 30283262 30283259 30283263 CAGCCTGGGCTACAGAACCAGACTCTGTCTCAAAAGAAAAAAAAAAAAAAGAAAGAAAGAAACAA CAGCCTGGGCTACAGAACCAGACTCTGTCTC____GAAAAAAAAAAAAAAGAAAGAAAGAAACAA CTTTT C SMG1P5 Ensembl:ENSG00000183604 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1447257149 Functional Loss DEL dbSNP153 32..35 33 - - - RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232,RMVar_hsa_circ_70636,RMVar_hsa_circ_110297,RMVar_hsa_circ_177862,RMVar_hsa_circ_328446 27088 RMVar_ID_27088 Human_SNP_ID_599459699 A-to-I Human chr16 - 30283338 30283338 30283338 TGGAGGCTGAGGTAGGAGAATTGCTTGAACCCAGGAAGTGGAGGTTGCAGTGAGCTGAGATCACA TGGAGGCTGAGGTAGGAGAATTGCTTGAACCCGGGAAGTGGAGGTTGCAGTGAGCTGAGATCACA T C SMG1P5 Ensembl:ENSG00000183604 Pseudogene intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1227557422 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17373264,Human_RBP_ID_17564102 RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232,RMVar_hsa_circ_70636,RMVar_hsa_circ_110297,RMVar_hsa_circ_177862,RMVar_hsa_circ_328446 27089 RMVar_ID_27089 Human_SNP_ID_599459865 A-to-I Human chr16 - 30283921 30283921 30283921 TGTTGTCACCTGGGCTGGAGTGCAGTGGTGCAATCTCGGCTCACTGCCACCTCTGCCTCCCGGGT TGTTGTCACCTGGGCTGGAGTGCAGTGGTGCAGTCTCGGCTCACTGCCACCTCTGCCTCCCGGGT T C SMG1P5 Ensembl:ENSG00000183604 Pseudogene intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1300347216 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17372293 RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232,RMVar_hsa_circ_70636,RMVar_hsa_circ_110297,RMVar_hsa_circ_177862,RMVar_hsa_circ_328446 27090 RMVar_ID_27090 Human_SNP_ID_599459866 A-to-I Human chr16 - 30283922 30283922 30283922 CTGTTGTCACCTGGGCTGGAGTGCAGTGGTGCAATCTCGGCTCACTGCCACCTCTGCCTCCCGGG CTGTTGTCACCTGGGCTGGAGTGCAGTGGTGCGATCTCGGCTCACTGCCACCTCTGCCTCCCGGG T C SMG1P5 Ensembl:ENSG00000183604 Pseudogene intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1230860457 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17372293 RMVar_hsa_circ_120916,RMVar_hsa_circ_177716,RMVar_hsa_circ_177732,RMVar_hsa_circ_92232,RMVar_hsa_circ_70636,RMVar_hsa_circ_110297,RMVar_hsa_circ_177862,RMVar_hsa_circ_328446 27091 RMVar_ID_27091 Human_SNP_ID_599483599 A-to-I Human chr16 - 30380434 30380434 30380434 AGCCAGGTGTGGTGGTGTGCACTTGTAGTCCCAGTTACTCAGGAGGCTGAGATGGGAGGATCACC AGCCAGGTGTGGTGGTGTGCACTTGTAGTCCCGGTTACTCAGGAGGCTGAGATGGGAGGATCACC T C SEPTIN1 Ensembl:ENSG00000180096 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs186083819 Functional Loss SNV dbSNP153 33..33 33 - - - 27092 RMVar_ID_27092 Human_SNP_ID_599485666 A-to-I Human chr16 + 30387612 30387612 30387612 GACAGAGTTTTCCTCGTCACCCAGGCTGGAGTACAATGGCGCGATCTCGGCTCACTGCAACCTCT GACAGAGTTTTCCTCGTCACCCAGGCTGGAGTGCAATGGCGCGATCTCGGCTCACTGCAACCTCT A G ZNF48 Ensembl:ENSG00000180035 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417794202 Functional Loss SNV dbSNP153 33..33 33 - - - 27093 RMVar_ID_27093 Human_SNP_ID_599496834 A-to-I Human chr16 - 30427889 30427889 30427889 TCAAACGATCCTCCCACCTCAGCCTTCGGAGTAGCTGGGTCTACAGGCGTGCGCCACCACCAAGC TCAAACGATCCTCCCACCTCAGCCTTCGGAGTTGCTGGGTCTACAGGCGTGCGCCACCACCAAGC T A DCTPP1 Ensembl:ENSG00000179958 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1278659914 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80015,RMVar_hsa_circ_122935,RMVar_hsa_circ_177879,RMVar_hsa_circ_177880 27094 RMVar_ID_27094 Human_SNP_ID_599509213 A-to-I Human chr16 + 30475899 30475899 30475899 TCAGCCTCCCAATTAGCTGGGACTATAGGCGCATGCTACCATGCCCAGCTAATTTTTATATTTTT TCAGCCTCCCAATTAGCTGGGACTATAGGCGCCTGCTACCATGCCCAGCTAATTTTTATATTTTT A C ITGAL Ensembl:ENSG00000005844 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1341086282 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86007,RMVar_hsa_circ_98934,RMVar_hsa_circ_177881,RMVar_hsa_circ_369439,RMVar_hsa_circ_177882,RMVar_hsa_circ_75607,RMVar_hsa_circ_107545,RMVar_hsa_circ_177883,RMVar_hsa_circ_177884,RMVar_hsa_circ_177885 27095 RMVar_ID_27095 Human_SNP_ID_599509214 A-to-I Human chr16 + 30475899 30475899 30475899 TCAGCCTCCCAATTAGCTGGGACTATAGGCGCATGCTACCATGCCCAGCTAATTTTTATATTTTT TCAGCCTCCCAATTAGCTGGGACTATAGGCGCGTGCTACCATGCCCAGCTAATTTTTATATTTTT A G ITGAL Ensembl:ENSG00000005844 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1341086282 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86007,RMVar_hsa_circ_98934,RMVar_hsa_circ_177881,RMVar_hsa_circ_369439,RMVar_hsa_circ_177882,RMVar_hsa_circ_75607,RMVar_hsa_circ_107545,RMVar_hsa_circ_177883,RMVar_hsa_circ_177884,RMVar_hsa_circ_177885 27096 RMVar_ID_27096 Human_SNP_ID_599511684 A-to-I Human chr16 + 30485651 30485651 30485651 GGCTCAGGTGATCCTCCCACGTAGCTGGGACTACAGGTGTGTGATACCACACCTGGCTAATTTTT GGCTCAGGTGATCCTCCCACGTAGCTGGGACTGCAGGTGTGTGATACCACACCTGGCTAATTTTT A G ITGAL Ensembl:ENSG00000005844 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1292065802 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86007,RMVar_hsa_circ_98934,RMVar_hsa_circ_177881,RMVar_hsa_circ_369439,RMVar_hsa_circ_177882,RMVar_hsa_circ_17761,RMVar_hsa_circ_87381,RMVar_hsa_circ_107545,RMVar_hsa_circ_177883,RMVar_hsa_circ_177885,RMVar_hsa_circ_127884,RMVar_hsa_circ_177889,RMVar_hsa_circ_177887,RMVar_hsa_circ_177888,RMVar_hsa_circ_92051,RMVar_hsa_circ_59739,RMVar_hsa_circ_350310,RMVar_hsa_circ_355696,RMVar_hsa_circ_18399,RMVar_hsa_circ_81430,RMVar_hsa_circ_2195,RMVar_hsa_circ_177891 27097 RMVar_ID_27097 Human_SNP_ID_599511744 A-to-I Human chr16 + 30485802 30485802 30485802 GCAATCTGCCCACCTCGGCCTCCTAAAGTGCTAGGATTACAGGCGTGAGCCACTGCACCCGGCCC GCAATCTGCCCACCTCGGCCTCCTAAAGTGCTGGGATTACAGGCGTGAGCCACTGCACCCGGCCC A G ITGAL Ensembl:ENSG00000005844 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs543243610 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86007,RMVar_hsa_circ_98934,RMVar_hsa_circ_177881,RMVar_hsa_circ_369439,RMVar_hsa_circ_177882,RMVar_hsa_circ_17761,RMVar_hsa_circ_87381,RMVar_hsa_circ_107545,RMVar_hsa_circ_177883,RMVar_hsa_circ_177885,RMVar_hsa_circ_127884,RMVar_hsa_circ_177889,RMVar_hsa_circ_177887,RMVar_hsa_circ_177888,RMVar_hsa_circ_92051,RMVar_hsa_circ_59739,RMVar_hsa_circ_350310,RMVar_hsa_circ_355696,RMVar_hsa_circ_18399,RMVar_hsa_circ_81430,RMVar_hsa_circ_2195,RMVar_hsa_circ_177891 27098 RMVar_ID_27098 Human_SNP_ID_599512692 A-to-I Human chr16 + 30489789 30489789 30489789 GAAACCCTGTCTCTACTAAAAATACAAAAGTTAGCCAGGCATGGTGGCGCATGCCTGTAGTCCCA GAAACCCTGTCTCTACTAAAAATACAAAAGTTCGCCAGGCATGGTGGCGCATGCCTGTAGTCCCA A C ITGAL Ensembl:ENSG00000005844 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1209612456 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86007,RMVar_hsa_circ_98934,RMVar_hsa_circ_177881,RMVar_hsa_circ_369439,RMVar_hsa_circ_177882,RMVar_hsa_circ_17761,RMVar_hsa_circ_87381,RMVar_hsa_circ_107545,RMVar_hsa_circ_177883,RMVar_hsa_circ_177885,RMVar_hsa_circ_177888,RMVar_hsa_circ_59739,RMVar_hsa_circ_355696,RMVar_hsa_circ_18399,RMVar_hsa_circ_55760,RMVar_hsa_circ_81430,RMVar_hsa_circ_2195,RMVar_hsa_circ_177891,RMVar_hsa_circ_112392,RMVar_hsa_circ_101347,RMVar_hsa_circ_177892,RMVar_hsa_circ_177893 27099 RMVar_ID_27099 Human_SNP_ID_599513681 A-to-I Human chr16 + 30493402 30493402 30493402 CCCAGGTTCACATTCTCCTGTCTCAGCCTCCCAAGTAGCTGGGACTACAGGCGCCTACCACCACG CCCAGGTTCACATTCTCCTGTCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCTACCACCACG A G ITGAL Ensembl:ENSG00000005844 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1484469021 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86007,RMVar_hsa_circ_98934,RMVar_hsa_circ_177881,RMVar_hsa_circ_369439,RMVar_hsa_circ_177882,RMVar_hsa_circ_17761,RMVar_hsa_circ_87381,RMVar_hsa_circ_107545,RMVar_hsa_circ_177883,RMVar_hsa_circ_177885,RMVar_hsa_circ_177888,RMVar_hsa_circ_59739,RMVar_hsa_circ_355696,RMVar_hsa_circ_18399,RMVar_hsa_circ_55760,RMVar_hsa_circ_81430,RMVar_hsa_circ_2195,RMVar_hsa_circ_177891,RMVar_hsa_circ_112392,RMVar_hsa_circ_101347,RMVar_hsa_circ_177892,RMVar_hsa_circ_177893 27100 RMVar_ID_27100 Human_SNP_ID_599516139 A-to-I Human chr16 + 30501798 30501798 30501798 ACGGTGGCTCATGCCAGCACTTTGAGAGGCTGAAGTAGGTGGATTGCTTGAGCTTAGGAGTTCAA ACGGTGGCTCATGCCAGCACTTTGAGAGGCTGCAGTAGGTGGATTGCTTGAGCTTAGGAGTTCAA A C ITGAL Ensembl:ENSG00000005844 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1484664112 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86007,RMVar_hsa_circ_177882,RMVar_hsa_circ_17761,RMVar_hsa_circ_87381,RMVar_hsa_circ_177888,RMVar_hsa_circ_18399,RMVar_hsa_circ_2386,RMVar_hsa_circ_81430,RMVar_hsa_circ_177891,RMVar_hsa_circ_73435,RMVar_hsa_circ_74334 27101 RMVar_ID_27101 Human_SNP_ID_599524195 A-to-I Human chr16 - 30530829 30530829 30530829 CTGGTCAGGACAACACCTGCCCAAGGAGAGCAAGGGCCTGTGACCTCTGCTGGCCTGTGCGCCCT CTGGTCAGGACAACACCTGCCCAAGGAGAGCAGGGGCCTGTGACCTCTGCTGGCCTGTGCGCCCT T C AC002310.4,ZNF747 Ensembl:ENSG00000261459,Ensembl:ENSG00000169955 Protein coding,Protein coding intron,3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1052527580 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12718643 27102 RMVar_ID_27102 Human_SNP_ID_599526173 A-to-I Human chr16 + 30536934 30536934 30536934 CACCATTCCCAGCTAATTTTTGTATTTTTAGTAGACACAGTGTTTCTCCATGTTGGTCAGGCTGG CACCATTCCCAGCTAATTTTTGTATTTTTAGTGGACACAGTGTTTCTCCATGTTGGTCAGGCTGG A G AC002310.1 Ensembl:ENSG00000235560 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1295230630 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12718736,Human_RBP_ID_26943062 Human_miRNA_ID_3153368,Human_miRNA_ID_3160724,Human_miRNA_ID_3216011 27103 RMVar_ID_27103 Human_SNP_ID_599530430 A-to-I Human chr16 - 30554361 30554361 30554361 AGTTCAAGCAATTCTCCTTCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCACCCACCACCTCCA AGTTCAAGCAATTCTCCTTCCTCAGCCTCCCAGGTAGCTGGGACTACAGGCACCCACCACCTCCA T C ZNF764 Ensembl:ENSG00000169951 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1181763664 Functional Loss SNV dbSNP153 33..33 33 - - - 27104 RMVar_ID_27104 Human_SNP_ID_599530431 A-to-I Human chr16 - 30554362 30554362 30554362 GAGTTCAAGCAATTCTCCTTCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCACCCACCACCTCC GAGTTCAAGCAATTCTCCTTCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCACCCACCACCTCC T C ZNF764 Ensembl:ENSG00000169951 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1388075073 Functional Loss SNV dbSNP153 33..33 33 - - - 27105 RMVar_ID_27105 Human_SNP_ID_599535340 A-to-I Human chr16 - 30570769 30570761 30570769 CAGCCTGGGTGACAGAGTGAGACTCCGTCTCAAAAATAAATAAATAAATAAATAAATAAATAAAT CAGCCTGGGTGACAGAGTGAGACTCCGTCTCA________TAAATAAATAAATAAATAAATAAAT ATTTATTTT A ZNF688 Ensembl:ENSG00000229809 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs200429164 Functional Loss DEL dbSNP153 33..40 33 - - - 27106 RMVar_ID_27106 Human_SNP_ID_599535344 A-to-I Human chr16 - 30570769 30570769 30570769 CAGCCTGGGTGACAGAGTGAGACTCCGTCTCAAAAATAAATAAATAAATAAATAAATAAATAAAT CAGCCTGGGTGACAGAGTGAGACTCCGTCTCATAAATAAATAAATAAATAAATAAATAAATAAAT T A ZNF688 Ensembl:ENSG00000229809 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1269008384 Functional Loss SNV dbSNP153 33..33 33 - - - 27107 RMVar_ID_27107 Human_SNP_ID_599537232 A-to-I Human chr16 + 30578114 30578114 30578114 TAATCCTACCACTTTGGGAGGCTCAGATAGACAGATCACTTGAGCCCATGAGTTCAAGACCAGCC TAATCCTACCACTTTGGGAGGCTCAGATAGACCGATCACTTGAGCCCATGAGTTCAAGACCAGCC A C AC002310.2 Ensembl:ENSG00000239791 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1443877000 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5247397 27108 RMVar_ID_27108 Human_SNP_ID_599537409 A-to-I Human chr16 + 30578894 30578894 30578894 CTCAGACTGAAGTGGCGCCATCATAGCTCACTATAGCCTCAAACTCCTGGGCTCAAGCTATCCTC CTCAGACTGAAGTGGCGCCATCATAGCTCACTGTAGCCTCAAACTCCTGGGCTCAAGCTATCCTC A G AC002310.2 Ensembl:ENSG00000239791 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251262669 Functional Loss SNV dbSNP153 33..33 33 - - - 27109 RMVar_ID_27109 Human_SNP_ID_599537566 A-to-I Human chr16 - 30579659 30579659 30579659 AATGGGAACTGGTGCCGGGCACGGTGGCTCACACCTGTGATCCCAGCACTGTGGGAGGCTGAGGC AATGGGAACTGGTGCCGGGCACGGTGGCTCACGCCTGTGATCCCAGCACTGTGGGAGGCTGAGGC T C ZNF785 Ensembl:ENSG00000197162 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1409458916 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1738142 27110 RMVar_ID_27110 Human_SNP_ID_599537737 A-to-I Human chr16 - 30580284 30580284 30580284 TCTTGGGAGGCTGAGGCAGAAGAATGGCTTGAACCCAGGAGGTGGAGGTTGCAGTGAGCCAACAT TCTTGGGAGGCTGAGGCAGAAGAATGGCTTGAGCCCAGGAGGTGGAGGTTGCAGTGAGCCAACAT T C ZNF785 Ensembl:ENSG00000197162 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1398389867 Functional Loss SNV dbSNP153 33..33 33 - - - 27111 RMVar_ID_27111 Human_SNP_ID_599537939 A-to-I Human chr16 - 30580995 30580994 30580996 CATGCCTGGCTAATTGCATTTTTACTAGAGACAGGTTTCACCATGTTGGCCAGGCTGGTCTCCAA CATGCCTGGCTAATTGCATTTTTACTAGAGA__GGTTTCACCATGTTGGCCAGGCTGGTCTCCAA CTG C ZNF785 Ensembl:ENSG00000197162 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1285982906 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_12719083 27112 RMVar_ID_27112 Human_SNP_ID_599537940 A-to-I Human chr16 - 30580995 30580995 30580995 CATGCCTGGCTAATTGCATTTTTACTAGAGACAGGTTTCACCATGTTGGCCAGGCTGGTCTCCAA CATGCCTGGCTAATTGCATTTTTACTAGAGACGGGTTTCACCATGTTGGCCAGGCTGGTCTCCAA T C ZNF785 Ensembl:ENSG00000197162 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs918940344 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12719083 27113 RMVar_ID_27113 Human_SNP_ID_599537962 A-to-I Human chr16 - 30581088 30581088 30581088 ATGATCTTGGCTCACTGCAACCTCCGCCTCCTAGGTTCAAGCGATTCTCCTGCCCCAGCCTCTTG ATGATCTTGGCTCACTGCAACCTCCGCCTCCTGGGTTCAAGCGATTCTCCTGCCCCAGCCTCTTG T C ZNF785 Ensembl:ENSG00000197162 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs113917399 Functional Loss SNV dbSNP153 33..33 33 - - - 27114 RMVar_ID_27114 Human_SNP_ID_599538186 A-to-I Human chr16 - 30581903 30581903 30581903 TTTTGTGCTGTTAGTAGAGACGGGGTTCCACCATCTTGGCCAGGCTGGTCTTGAATTCCTGACCT TTTTGTGCTGTTAGTAGAGACGGGGTTCCACCTTCTTGGCCAGGCTGGTCTTGAATTCCTGACCT T A ZNF785 Ensembl:ENSG00000197162 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1008659063 Functional Loss SNV dbSNP153 33..33 33 - - - 27115 RMVar_ID_27115 Human_SNP_ID_599538192 A-to-I Human chr16 - 30581923 30581923 30581923 CGCCACCAGGCCCAGCTAATTTTTGTGCTGTTAGTAGAGACGGGGTTCCACCATCTTGGCCAGGC CGCCACCAGGCCCAGCTAATTTTTGTGCTGTTGGTAGAGACGGGGTTCCACCATCTTGGCCAGGC T C ZNF785 Ensembl:ENSG00000197162 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017799623 Functional Loss SNV dbSNP153 33..33 33 - - - 27116 RMVar_ID_27116 Human_SNP_ID_599539819 A-to-I Human chr16 + 30587269 30587269 30587269 CTACTAAAACAGAAAAATTAGCCAGGTGTGGTAGTGCACCCCTGTAATTCCAGCTACTTGGGGGG CTACTAAAACAGAAAAATTAGCCAGGTGTGGTGGTGCACCCCTGTAATTCCAGCTACTTGGGGGG A G AC093249.2 Ensembl:ENSG00000260167 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1333315985 Functional Loss SNV dbSNP153 33..33 33 - - - 27117 RMVar_ID_27117 Human_SNP_ID_599539823 A-to-I Human chr16 + 30587282 30587282 30587282 AAAATTAGCCAGGTGTGGTAGTGCACCCCTGTAATTCCAGCTACTTGGGGGGCTGAGGCATGAGA AAAATTAGCCAGGTGTGGTAGTGCACCCCTGTGATTCCAGCTACTTGGGGGGCTGAGGCATGAGA A G AC093249.2 Ensembl:ENSG00000260167 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1233062883 Functional Loss SNV dbSNP153 33..33 33 - - - 27118 RMVar_ID_27118 Human_SNP_ID_599540319 A-to-I Human chr16 + 30589412 30589412 30589412 CCTGTGTCACCCAGACTGGAGTGCAGCAGTGCAATCTCAGGTCACTGCAACCTCCACCTCCTGGG CCTGTGTCACCCAGACTGGAGTGCAGCAGTGCGATCTCAGGTCACTGCAACCTCCACCTCCTGGG A G AC093249.2 Ensembl:ENSG00000260167 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1453311553 Functional Loss SNV dbSNP153 33..33 33 - - - 27119 RMVar_ID_27119 Human_SNP_ID_599544904 A-to-I Human chr16 - 30607875 30607875 30607875 TCACTGTAACCTCTTGCTCCCGGTTTCAAGCAATTCTCCTGTCTCAGCCTCTGGAGTAGGTGGGA TCACTGTAACCTCTTGCTCCCGGTTTCAAGCACTTCTCCTGTCTCAGCCTCTGGAGTAGGTGGGA T G ZNF689 Ensembl:ENSG00000156853 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1377705393 Functional Loss SNV dbSNP153 33..33 33 - - - 27120 RMVar_ID_27120 Human_SNP_ID_599545012 A-to-I Human chr16 - 30608357 30608357 30608357 GGAGAATTGCTTGATCCTGGGAGGTGGAAGTTACAGTGAGCCGAGATCATGCCAGTGTACTCCAG GGAGAATTGCTTGATCCTGGGAGGTGGAAGTTGCAGTGAGCCGAGATCATGCCAGTGTACTCCAG T C ZNF689 Ensembl:ENSG00000156853 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1467308229 Functional Loss SNV dbSNP153 33..33 33 - - - 27121 RMVar_ID_27121 Human_SNP_ID_599545038 A-to-I Human chr16 - 30608483 30608483 30608483 GAGGTCCGGAGTTCAAGACCAGCCTGACCAACATCGTGAAACCCCGTCTCTACTAAAAAAATACA GAGGTCCGGAGTTCAAGACCAGCCTGACCAACGTCGTGAAACCCCGTCTCTACTAAAAAAATACA T C ZNF689 Ensembl:ENSG00000156853 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1413585951 Functional Loss SNV dbSNP153 33..33 33 - - - 27122 RMVar_ID_27122 Human_SNP_ID_599581862 A-to-I Human chr16 + 30730946 30730946 30730946 TGCCTCGGCCTTCCAAAGTGCTGGGATTACACACGTGAGCCATTGCACCCAGCCTTAAGGGACCA TGCCTCGGCCTTCCAAAGTGCTGGGATTACACGCGTGAGCCATTGCACCCAGCCTTAAGGGACCA A G AC106886.6,SRCAP Ensembl:ENSG00000282034,Ensembl:ENSG00000080603 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs9934046 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12873656 GWAS_ID_2776,GWAS_ID_2777 RMVar_hsa_circ_269023,RMVar_hsa_circ_101421,RMVar_hsa_circ_104376,RMVar_hsa_circ_177924,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_177947,RMVar_hsa_circ_42150,RMVar_hsa_circ_273386,RMVar_hsa_circ_314412,RMVar_hsa_circ_360349,RMVar_hsa_circ_302438,RMVar_hsa_circ_177957 27123 RMVar_ID_27123 Human_SNP_ID_599582360 A-to-I Human chr16 + 30733016 30733016 30733016 CGCCATCACGCCCAGCTAATTTTTGTGTTTTTAGTAGAGACAGGGTCTCATCATGTTGGCCAGGC CGCCATCACGCCCAGCTAATTTTTGTGTTTTTGGTAGAGACAGGGTCTCATCATGTTGGCCAGGC A G AC106886.6,SRCAP Ensembl:ENSG00000282034,Ensembl:ENSG00000080603 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1370245849 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269023,RMVar_hsa_circ_101421,RMVar_hsa_circ_104376,RMVar_hsa_circ_177924,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_177947,RMVar_hsa_circ_42150,RMVar_hsa_circ_273386,RMVar_hsa_circ_314412,RMVar_hsa_circ_360349,RMVar_hsa_circ_302438,RMVar_hsa_circ_177957 27124 RMVar_ID_27124 Human_SNP_ID_599589334 A-to-I Human chr16 + 30754349 30754349 30754349 CACTACGCCTGGCTCATTTTTGTATTTTTAGTAGAGATGGAATTTCACAATGTTGGCCAGGCTGG CACTACGCCTGGCTCATTTTTGTATTTTTAGTGGAGATGGAATTTCACAATGTTGGCCAGGCTGG A G PHKG2 Ensembl:ENSG00000156873 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1328539636 Functional Loss SNV dbSNP153 33..33 33 - - - 27125 RMVar_ID_27125 Human_SNP_ID_599595171 A-to-I Human chr16 + 30770805 30770805 30770805 TCGGTCTCAGTTCACTGCAACCTCCGCCTCCCAGGTTCAAGCGATTCTTCTGCCTTAGTGTCCCG TCGGTCTCAGTTCACTGCAACCTCCGCCTCCCTGGTTCAAGCGATTCTTCTGCCTTAGTGTCCCG A T RNF40 Ensembl:ENSG00000103549 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1457737574 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266434,RMVar_hsa_circ_98224,RMVar_hsa_circ_177970 27126 RMVar_ID_27126 Human_SNP_ID_599595206 A-to-I Human chr16 + 30770970 30770969 30770970 CTGACATCGTGATTTGCCCGCCTTGGCCTCCCAAAGTGTTGGGATTACAAGTGTGAGCCACTGTG CTGACATCGTGATTTGCCCGCCTTGGCCTCCTGAAGTGTTGGGATTACAAGTGTGAGCCACTGTG CA TG RNF40 Ensembl:ENSG00000103549 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs386790274 Functional Loss MNV dbSNP153 32..33 33 - - - RMVar_hsa_circ_266434,RMVar_hsa_circ_98224,RMVar_hsa_circ_177970 27127 RMVar_ID_27127 Human_SNP_ID_599595207 A-to-I Human chr16 + 30770970 30770970 30770970 CTGACATCGTGATTTGCCCGCCTTGGCCTCCCAAAGTGTTGGGATTACAAGTGTGAGCCACTGTG CTGACATCGTGATTTGCCCGCCTTGGCCTCCCGAAGTGTTGGGATTACAAGTGTGAGCCACTGTG A G RNF40 Ensembl:ENSG00000103549 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs8056105 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266434,RMVar_hsa_circ_98224,RMVar_hsa_circ_177970 27128 RMVar_ID_27128 Human_SNP_ID_599619464 A-to-I Human chr16 - 30866819 30866819 30866819 GAACTCTTGGCCTTATATAATCCTCCCACCTCAGCTTCCCAAAGTGCTGGCATTACAGGCATGAG GAACTCTTGGCCTTATATAATCCTCCCACCTCGGCTTCCCAAAGTGCTGGCATTACAGGCATGAG T C BCL7C Ensembl:ENSG00000099385 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1322951453 Functional Loss SNV dbSNP153 33..33 33 - - - 27129 RMVar_ID_27129 Human_SNP_ID_599620118 A-to-I Human chr16 - 30869410 30869410 30869410 ACTAGAGCTTAGGAGTTCGAGGCCAGCAACATAGTGAGAACTCATCTCTACAAAAAGTAAAAAAA ACTAGAGCTTAGGAGTTCGAGGCCAGCAACATGGTGAGAACTCATCTCTACAAAAAGTAAAAAAA T C BCL7C Ensembl:ENSG00000099385 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1246364922 Functional Loss SNV dbSNP153 33..33 33 - - - 27130 RMVar_ID_27130 Human_SNP_ID_599632043 A-to-I Human chr16 - 30917429 30917429 30917429 AGGCTGGTGTGAAGTGGTGCAGTCATAGTTCAATGCAGCCTCGACCTCCTGGGCTCAAGTGATCT AGGCTGGTGTGAAGTGGTGCAGTCATAGTTCAGTGCAGCCTCGACCTCCTGGGCTCAAGTGATCT T C FBXL19-AS1,FBXL19-AS1:2 RNACentral:URS0000D5770D,RNACentral:URS0000D5C8FD lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1220159766 Functional Loss SNV dbSNP153 33..33 33 - - - 27131 RMVar_ID_27131 Human_SNP_ID_599633040 A-to-I Human chr16 - 30920027 30920027 30920027 AAAATTAGCCAGGTGTAGTGGTGTGCACCTGTAGTCCCAGCTCTTCAGGAGGCTGAGAAAAGAGA AAAATTAGCCAGGTGTAGTGGTGTGCACCTGTGGTCCCAGCTCTTCAGGAGGCTGAGAAAAGAGA T C FBXL19-AS1 Ensembl:ENSG00000260852 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1435526636 Functional Loss SNV dbSNP153 33..33 33 - - - 27132 RMVar_ID_27132 Human_SNP_ID_599633118 A-to-I Human chr16 - 30920340 30920340 30920340 TGTAGTCCCAGCTACTTAGGAGGCTGAGGGGCAAGGATTGCTTGAGGCTGAGAGATTGAGCCTGC TGTAGTCCCAGCTACTTAGGAGGCTGAGGGGCCAGGATTGCTTGAGGCTGAGAGATTGAGCCTGC T G FBXL19-AS1 Ensembl:ENSG00000260852 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1007738783 Functional Loss SNV dbSNP153 33..33 33 - - - 27133 RMVar_ID_27133 Human_SNP_ID_599633322 A-to-I Human chr16 - 30921343 30921343 30921343 TTGCCCAGGCTGGTCTCGAACTCCTGGCCACAAGTGTGCCTCCCGCCTTGGCCTCCCTAAGTGTT TTGCCCAGGCTGGTCTCGAACTCCTGGCCACACGTGTGCCTCCCGCCTTGGCCTCCCTAAGTGTT T G FBXL19-AS1 Ensembl:ENSG00000260852 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs916994944 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17564107,Human_RBP_ID_23307522 Human_miRNA_ID_3177933,Human_miRNA_ID_3206787 27134 RMVar_ID_27134 Human_SNP_ID_599633372 A-to-I Human chr16 - 30921518 30921518 30921518 TCACTTGGGTTGGAGTGCAGTTGCAGGATCATAGTTTGCTGCAGCCTCGACCTCCTGGGCTTAAG TCACTTGGGTTGGAGTGCAGTTGCAGGATCATCGTTTGCTGCAGCCTCGACCTCCTGGGCTTAAG T G FBXL19-AS1 Ensembl:ENSG00000260852 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1380897653 Functional Loss SNV dbSNP153 33..33 33 - - - 27135 RMVar_ID_27135 Human_SNP_ID_599637056 A-to-I Human chr16 + 30933503 30933503 30933503 AGAGGGTCTCTCTCTGTTGCCCAGGCTGGAGTACAGTGGTGCAGTCATAGCTCATTGCAGCTTCA AGAGGGTCTCTCTCTGTTGCCCAGGCTGGAGTTCAGTGGTGCAGTCATAGCTCATTGCAGCTTCA A T FBXL19 Ensembl:ENSG00000099364 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1304323964 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5070,RMVar_hsa_circ_101190,RMVar_hsa_circ_177980 27136 RMVar_ID_27136 Human_SNP_ID_599637169 A-to-I Human chr16 + 30933898 30933898 30933898 CCTCAGCCTCCCGAGTAGCTGGGATTACAGACATGCGCCACTATGCCTGGCTAATTTTGTATTTT CCTCAGCCTCCCGAGTAGCTGGGATTACAGACGTGCGCCACTATGCCTGGCTAATTTTGTATTTT A G FBXL19 Ensembl:ENSG00000099364 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs938652007 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5070,RMVar_hsa_circ_101190,RMVar_hsa_circ_177980 27137 RMVar_ID_27137 Human_SNP_ID_599637249 A-to-I Human chr16 + 30934197 30934197 30934197 CAGCCTCGCCAACATGGTGAGACCCTGTCTCTACTAGAAATACAAAAAATTTAGCCAGGCATGGT CAGCCTCGCCAACATGGTGAGACCCTGTCTCTGCTAGAAATACAAAAAATTTAGCCAGGCATGGT A G FBXL19 Ensembl:ENSG00000099364 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1265215595 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5070,RMVar_hsa_circ_101190,RMVar_hsa_circ_177980 27138 RMVar_ID_27138 Human_SNP_ID_599638635 A-to-I Human chr16 + 30939553 30939553 30939553 CTCCTGCCTCAGCCTCCCGAGTATCTGGGACTACAGGCGCCCTCCACCACGCCCAGCTAATTTTT CTCCTGCCTCAGCCTCCCGAGTATCTGGGACTGCAGGCGCCCTCCACCACGCCCAGCTAATTTTT A G FBXL19 Ensembl:ENSG00000099364 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1271924667 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5070,RMVar_hsa_circ_101190,RMVar_hsa_circ_177980 27139 RMVar_ID_27139 Human_SNP_ID_599639661 A-to-I Human chr16 + 30943777 30943777 30943777 TGCCCACCTCTGCCTTCCAAAGTGTTGGGATTATAGGCGTGAGCCACCACACCTGGCCAAAAGAA TGCCCACCTCTGCCTTCCAAAGTGTTGGGATTGTAGGCGTGAGCCACCACACCTGGCCAAAAGAA A G FBXL19 Ensembl:ENSG00000099364 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1319595186 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19149 27140 RMVar_ID_27140 Human_SNP_ID_599639662 A-to-I Human chr16 + 30943777 30943777 30943777 TGCCCACCTCTGCCTTCCAAAGTGTTGGGATTATAGGCGTGAGCCACCACACCTGGCCAAAAGAA TGCCCACCTCTGCCTTCCAAAGTGTTGGGATTTTAGGCGTGAGCCACCACACCTGGCCAAAAGAA A T FBXL19 Ensembl:ENSG00000099364 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1319595186 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19149 27141 RMVar_ID_27141 Human_SNP_ID_599642230 A-to-I Human chr16 + 30952946 30952946 30952946 CTTTGGCCTCCCAAAGTGCTGGGATTATAGGCATGAACCGCCGCGCCCGGCCATCCAGCCCTCTT CTTTGGCCTCCCAAAGTGCTGGGATTATAGGCCTGAACCGCCGCGCCCGGCCATCCAGCCCTCTT A C AC135048.1,ORAI3 Ensembl:ENSG00000261487,Ensembl:ENSG00000175938 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1401530030 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12722850 RMVar_hsa_circ_82084,RMVar_hsa_circ_177982 27142 RMVar_ID_27142 Human_SNP_ID_599667757 A-to-I Human chr16 + 31040719 31040719 31040719 CATAAGCGTTTAGGCAGGGTGTGGTGGCTCGCACCAGTAATCCCAGCACTTTGGGAGGCCCAGGC CATAAGCGTTTAGGCAGGGTGTGGTGGCTCGCGCCAGTAATCCCAGCACTTTGGGAGGCCCAGGC A G STX4 Ensembl:ENSG00000103496 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1448885196 Functional Loss SNV dbSNP153 33..33 33 - - - 27143 RMVar_ID_27143 Human_SNP_ID_599667889 A-to-I Human chr16 + 31041265 31041265 31041265 ACTATCTCAGCTCACTGCAAGCTCCGTCTCCCAGGTTCACGCCATTCTCCTGCCTCAGCCTCCCG ACTATCTCAGCTCACTGCAAGCTCCGTCTCCCGGGTTCACGCCATTCTCCTGCCTCAGCCTCCCG A G STX4 Ensembl:ENSG00000103496 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1169919202 Functional Loss SNV dbSNP153 33..33 33 - - - 27144 RMVar_ID_27144 Human_SNP_ID_599671162 A-to-I Human chr16 - 31054494 31054492 31054495 AATTCTTATTCTTGTGCCTCAGCCTCCCGAGTAGCCGGGACTGCAGGCATGCACCACCACACCTG AATTCTTATTCTTGTGCCTCAGCCTCCCGAG___CCGGGACTGCAGGCATGCACCACCACACCTG GCTA G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1328197719 Functional Loss DEL dbSNP153 32..34 33 - - - 27145 RMVar_ID_27145 Human_SNP_ID_599673843 A-to-I Human chr16 - 31063412 31063412 31063412 ATGACATGTTTCTAGGCTGGGCACAATAGCTCACGCCTATAATTCCAGCACTTTGGGAGGCTGAG ATGACATGTTTCTAGGCTGGGCACAATAGCTCGCGCCTATAATTCCAGCACTTTGGGAGGCTGAG T C ZNF668 Ensembl:ENSG00000167394 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1213251746 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99732,RMVar_hsa_circ_178002 27146 RMVar_ID_27146 Human_SNP_ID_599682837 A-to-I Human chr16 - 31091022 31091022 31091022 CTAGAAGGCCCTAGATGTGGGGCTTCTAGATTACCCCCTCCTCCTGCCATACCCGCACATGACAA CTAGAAGGCCCTAGATGTGGGGCTTCTAGATTCCCCCCTCCTCCTGCCATACCCGCACATGACAA T G VKORC1,AC135050.2 Ensembl:ENSG00000167397,Ensembl:ENSG00000255439 Protein coding,Protein coding 3'UTR,intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs941300305 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_473308,Human_RBP_ID_17488255,Human_RBP_ID_17653014,Human_RBP_ID_20116508,Human_RBP_ID_22497803 RMVar_hsa_circ_78397,RMVar_hsa_circ_101354,RMVar_hsa_circ_178005,RMVar_hsa_circ_339746,RMVar_hsa_circ_119903,RMVar_hsa_circ_105709,RMVar_hsa_circ_80636,RMVar_hsa_circ_178006,RMVar_hsa_circ_178008,RMVar_hsa_circ_178009,RMVar_hsa_circ_178007 27147 RMVar_ID_27147 Human_SNP_ID_599683318 A-to-I Human chr16 - 31092813 31092813 31092813 CCCAGGCTGGTCTCAAGCAATCTGTCTGCCTCAGCCTCCCAAAGTGCTGGGGGGATTACAGGCGT CCCAGGCTGGTCTCAAGCAATCTGTCTGCCTCGGCCTCCCAAAGTGCTGGGGGGATTACAGGCGT T C VKORC1,AC135050.2 Ensembl:ENSG00000167397,Ensembl:ENSG00000255439 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1349483563 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1704956,Human_Splice_Rec_1704957 Human_miRNA_ID_2715658,Human_miRNA_ID_3051640 RMVar_hsa_circ_78397,RMVar_hsa_circ_105709,RMVar_hsa_circ_80636,RMVar_hsa_circ_178008,RMVar_hsa_circ_178009,RMVar_hsa_circ_178007 27148 RMVar_ID_27148 Human_SNP_ID_599691762 A-to-I Human chr16 + 31121220 31121220 31121220 TCGGCTCACTGTAAACTCCGCCACCTGGGTTCAAGCAATTTTCCTGTCTCAGCCTCCCAAGTAGC TCGGCTCACTGTAAACTCCGCCACCTGGGTTCGAGCAATTTTCCTGTCTCAGCCTCCCAAGTAGC A G KAT8 Ensembl:ENSG00000103510 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs902209607 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6509095,Human_RBP_ID_12723966,Human_RBP_ID_23687338,Human_RBP_ID_27442161 RMVar_hsa_circ_54419,RMVar_hsa_circ_282795,RMVar_hsa_circ_178015 27149 RMVar_ID_27149 Human_SNP_ID_599691770 A-to-I Human chr16 + 31121260 31121260 31121260 TTCCTGTCTCAGCCTCCCAAGTAGCTAGGACTACAGGTACCTGCCACCACGCCCGGATAATTTTT TTCCTGTCTCAGCCTCCCAAGTAGCTAGGACTGCAGGTACCTGCCACCACGCCCGGATAATTTTT A G KAT8 Ensembl:ENSG00000103510 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs916970579 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12723969,Human_RBP_ID_23687340 RMVar_hsa_circ_54419,RMVar_hsa_circ_282795,RMVar_hsa_circ_178015 27150 RMVar_ID_27150 Human_SNP_ID_599691896 A-to-I Human chr16 + 31121664 31121664 31121664 GAACTCCTGGGCTCAAATGTTCTTCCTGCCTTAGCCTTCTAAGTAGCTGGGACTACAGGAGTGCA GAACTCCTGGGCTCAAATGTTCTTCCTGCCTTGGCCTTCTAAGTAGCTGGGACTACAGGAGTGCA A G KAT8 Ensembl:ENSG00000103510 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1333147301 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3494433,Human_RBP_ID_12723987 RMVar_hsa_circ_54419,RMVar_hsa_circ_282795,RMVar_hsa_circ_178015 27151 RMVar_ID_27151 Human_SNP_ID_599691897 A-to-I Human chr16 + 31121664 31121664 31121664 GAACTCCTGGGCTCAAATGTTCTTCCTGCCTTAGCCTTCTAAGTAGCTGGGACTACAGGAGTGCA GAACTCCTGGGCTCAAATGTTCTTCCTGCCTTTGCCTTCTAAGTAGCTGGGACTACAGGAGTGCA A T KAT8 Ensembl:ENSG00000103510 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1333147301 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3494433,Human_RBP_ID_12723987 RMVar_hsa_circ_54419,RMVar_hsa_circ_282795,RMVar_hsa_circ_178015 27152 RMVar_ID_27152 Human_SNP_ID_599691927 A-to-I Human chr16 + 31121772 31121772 31121772 ATTGTACATATTATTGTTATTTTTTTTTTTTGAGACAGCGTCTTACTCTATCGTCTAGGCTGAGT ATTGTACATATTATTGTTATTTTTTTTTTTTGTGACAGCGTCTTACTCTATCGTCTAGGCTGAGT A T KAT8 Ensembl:ENSG00000103510 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1353893245 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9825082,Human_RBP_ID_12723999,Human_RBP_ID_23307526 RMVar_hsa_circ_54419,RMVar_hsa_circ_282795,RMVar_hsa_circ_178015 27153 RMVar_ID_27153 Human_SNP_ID_599692118 A-to-I Human chr16 + 31122518 31122518 31122518 CTATTGTAATGGAAATGTTCTATAGCTGTACTATCTAGTACCGTAGCCACTAGCCACATGTAGCT CTATTGTAATGGAAATGTTCTATAGCTGTACTGTCTAGTACCGTAGCCACTAGCCACATGTAGCT A G AC135050.6,KAT8 Ensembl:ENSG00000278133,Ensembl:ENSG00000103510 lincRNA,Protein coding exon,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1137606 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3494434,Human_RBP_ID_12724041,Human_RBP_ID_18285379,Human_RBP_ID_26440968 Human_miRNA_ID_3166752 RMVar_hsa_circ_54419,RMVar_hsa_circ_282795,RMVar_hsa_circ_178015 27154 RMVar_ID_27154 Human_SNP_ID_599692145 A-to-I Human chr16 + 31122646 31122646 31122646 TTACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGTGGATCACCAGGTCAGAAGATCGAG TTACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGTGGATCACCAGGTCAGAAGATCGAG A G AC135050.6,KAT8 Ensembl:ENSG00000278133,Ensembl:ENSG00000103510 lincRNA,Protein coding intron,intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1334455399 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54419,RMVar_hsa_circ_282795,RMVar_hsa_circ_178015 27155 RMVar_ID_27155 Human_SNP_ID_599692167 A-to-I Human chr16 + 31122691 31122691 31122691 CACCAGGTCAGAAGATCGAGACCATCCCGGCTAACATGGTGAAACCCCATCTCTACTGAAAAATA CACCAGGTCAGAAGATCGAGACCATCCCGGCTGACATGGTGAAACCCCATCTCTACTGAAAAATA A G AC135050.6,KAT8 Ensembl:ENSG00000278133,Ensembl:ENSG00000103510 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1054402689 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54419,RMVar_hsa_circ_282795,RMVar_hsa_circ_178015 27156 RMVar_ID_27156 Human_SNP_ID_599692168 A-to-I Human chr16 + 31122694 31122694 31122694 CAGGTCAGAAGATCGAGACCATCCCGGCTAACATGGTGAAACCCCATCTCTACTGAAAAATACAA CAGGTCAGAAGATCGAGACCATCCCGGCTAACGTGGTGAAACCCCATCTCTACTGAAAAATACAA A G AC135050.6,KAT8 Ensembl:ENSG00000278133,Ensembl:ENSG00000103510 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs981941446 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12724047 RMVar_hsa_circ_54419,RMVar_hsa_circ_282795,RMVar_hsa_circ_178015 27157 RMVar_ID_27157 Human_SNP_ID_599692198 A-to-I Human chr16 + 31122766 31122766 31122766 AGCCGGGCGTGGTGGCGTGCACCTGTAGTCCCAGCTACTCGGGAGGCTGAGGTAGGAGAATGGCG AGCCGGGCGTGGTGGCGTGCACCTGTAGTCCCGGCTACTCGGGAGGCTGAGGTAGGAGAATGGCG A G AC135050.6,KAT8 Ensembl:ENSG00000278133,Ensembl:ENSG00000103510 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1346338817 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54419,RMVar_hsa_circ_282795,RMVar_hsa_circ_178015 27158 RMVar_ID_27158 Human_SNP_ID_599692328 A-to-I Human chr16 + 31123240 31123239 31123241 TTAAAAAAATTTTATTTTTATTTTTTCGAGACAGAGTCTCACTCTGTTAACCAGGCTGGAGTGCA TTAAAAAAATTTTATTTTTATTTTTTCGAGAC__AGTCTCACTCTGTTAACCAGGCTGGAGTGCA CAG C AC135050.6,KAT8 Ensembl:ENSG00000278133,Ensembl:ENSG00000103510 lincRNA,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1426370888 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_54419,RMVar_hsa_circ_282795,RMVar_hsa_circ_178015 27159 RMVar_ID_27159 Human_SNP_ID_599692329 A-to-I Human chr16 + 31123248 31123244 31123248 ATTTTATTTTTATTTTTTCGAGACAGAGTCTCACTCTGTTAACCAGGCTGGAGTGCAGTGGTGCG ATTTTATTTTTATTTTTTCGAGACAGAGT____CTCTGTTAACCAGGCTGGAGTGCAGTGGTGCG TCTCA T AC135050.6,KAT8 Ensembl:ENSG00000278133,Ensembl:ENSG00000103510 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1258609158 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_54419,RMVar_hsa_circ_282795,RMVar_hsa_circ_178015 27160 RMVar_ID_27160 Human_SNP_ID_599692348 A-to-I Human chr16 + 31123310 31123310 31123310 GCGATCTCAGCTCACTGCAACCTCCGCCTCCCAGATTCAAGTGAGTTTCCTGCCGCAGCCTCCCA GCGATCTCAGCTCACTGCAACCTCCGCCTCCCGGATTCAAGTGAGTTTCCTGCCGCAGCCTCCCA A G AC135050.6,KAT8 Ensembl:ENSG00000278133,Ensembl:ENSG00000103510 lincRNA,Protein coding intron,intron GSE38233;GSE100210;GSE99789 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 24183664,29129909,29796672 RNA-Seq:(High) rs1454445183 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54419,RMVar_hsa_circ_282795,RMVar_hsa_circ_178015 27161 RMVar_ID_27161 Human_SNP_ID_599692351 A-to-I Human chr16 + 31123316 31123316 31123316 TCAGCTCACTGCAACCTCCGCCTCCCAGATTCAAGTGAGTTTCCTGCCGCAGCCTCCCAAGTAGC TCAGCTCACTGCAACCTCCGCCTCCCAGATTCTAGTGAGTTTCCTGCCGCAGCCTCCCAAGTAGC A T AC135050.6,KAT8 Ensembl:ENSG00000278133,Ensembl:ENSG00000103510 lincRNA,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1372176043 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54419,RMVar_hsa_circ_282795,RMVar_hsa_circ_178015 27162 RMVar_ID_27162 Human_SNP_ID_599692363 A-to-I Human chr16 + 31123356 31123356 31123356 TTCCTGCCGCAGCCTCCCAAGTAGCTGGGACTACAGGCACGCACCATCATGCCTGGCTAATTTTT TTCCTGCCGCAGCCTCCCAAGTAGCTGGGACTGCAGGCACGCACCATCATGCCTGGCTAATTTTT A G AC135050.6,KAT8 Ensembl:ENSG00000278133,Ensembl:ENSG00000103510 lincRNA,Protein coding intron,intron GSE38233;GSE99789;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29796672,32596459 RNA-Seq:(High) rs1450407117 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54419,RMVar_hsa_circ_282795,RMVar_hsa_circ_178015 27163 RMVar_ID_27163 Human_SNP_ID_599692366 A-to-I Human chr16 + 31123362 31123362 31123362 CCGCAGCCTCCCAAGTAGCTGGGACTACAGGCACGCACCATCATGCCTGGCTAATTTTTGTATTT CCGCAGCCTCCCAAGTAGCTGGGACTACAGGCGCGCACCATCATGCCTGGCTAATTTTTGTATTT A G AC135050.6,KAT8 Ensembl:ENSG00000278133,Ensembl:ENSG00000103510 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs34059030 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54419,RMVar_hsa_circ_282795,RMVar_hsa_circ_178015 27164 RMVar_ID_27164 Human_SNP_ID_599692377 A-to-I Human chr16 + 31123391 31123391 31123391 GGCACGCACCATCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGATAGGGTTTCACTATGTTTG GGCACGCACCATCATGCCTGGCTAATTTTTGTGTTTTTAGTAGAGATAGGGTTTCACTATGTTTG A G AC135050.6,KAT8 Ensembl:ENSG00000278133,Ensembl:ENSG00000103510 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs182907498 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5247698 RMVar_hsa_circ_54419,RMVar_hsa_circ_282795,RMVar_hsa_circ_178015 27165 RMVar_ID_27165 Human_SNP_ID_599692414 A-to-I Human chr16 + 31123528 31123528 31123528 ACCGTGCCCAGCCAAAATTTTCATTTTTTGAGACAGAGTCTCACTCTGTCACCTAGGCGGGAGTA ACCGTGCCCAGCCAAAATTTTCATTTTTTGAGGCAGAGTCTCACTCTGTCACCTAGGCGGGAGTA A G AC135050.6,KAT8 Ensembl:ENSG00000278133,Ensembl:ENSG00000103510 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1332474532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5247599,Human_RBP_ID_12724062,Human_RBP_ID_17564111,Human_RBP_ID_23164036 RMVar_hsa_circ_54419,RMVar_hsa_circ_282795,RMVar_hsa_circ_178015 27166 RMVar_ID_27166 Human_SNP_ID_599692417 A-to-I Human chr16 + 31123538 31123534 31123538 GCCAAAATTTTCATTTTTTGAGACAGAGTCTCACTCTGTCACCTAGGCGGGAGTACAGTGGCGAG GCCAAAATTTTCATTTTTTGAGACAGAGT____CTCTGTCACCTAGGCGGGAGTACAGTGGCGAG TCTCA T AC135050.6,KAT8 Ensembl:ENSG00000278133,Ensembl:ENSG00000103510 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1327756213 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_5247599,Human_RBP_ID_17564111,Human_RBP_ID_23164036 RMVar_hsa_circ_54419,RMVar_hsa_circ_282795,RMVar_hsa_circ_178015 27167 RMVar_ID_27167 Human_SNP_ID_599692439 A-to-I Human chr16 + 31123641 31123638 31123642 CAATTTTTGTGCCTCAGCCTCCCAAGTATCTGAGATTACAGGCGTGTGCCACCACACCCAGCTAT CAATTTTTGTGCCTCAGCCTCCCAAGTATC____ATTACAGGCGTGTGCCACCACACCCAGCTAT CTGAG C AC135050.6,KAT8 Ensembl:ENSG00000278133,Ensembl:ENSG00000103510 lincRNA,Protein coding intron,intron GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs1272317872 Functional Loss DEL dbSNP153 31..34 33 - - - RMVar_hsa_circ_54419,RMVar_hsa_circ_282795,RMVar_hsa_circ_178015 27168 RMVar_ID_27168 Human_SNP_ID_599692470 A-to-I Human chr16 + 31123773 31123773 31123773 GCCTCAAGTGGTCCTCCCACCTCGGCCTCTCAAAGTGCTGGGATTACAGGCGTGAGCCACCACGT GCCTCAAGTGGTCCTCCCACCTCGGCCTCTCAGAGTGCTGGGATTACAGGCGTGAGCCACCACGT A G AC135050.6,KAT8 Ensembl:ENSG00000278133,Ensembl:ENSG00000103510 lincRNA,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1142000 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17564673,Human_RBP_ID_26446065 RMVar_hsa_circ_54419,RMVar_hsa_circ_282795,RMVar_hsa_circ_178015 27169 RMVar_ID_27169 Human_SNP_ID_599709672 A-to-I Human chr16 + 31182742 31182742 31182742 TTGCTTTTCTTTTTCTTGTTTTTTGGAGACGGAGTCTGGTCCTGTTGCCCAGGCTGGAGTGCAGT TTGCTTTTCTTTTTCTTGTTTTTTGGAGACGGCGTCTGGTCCTGTTGCCCAGGCTGGAGTGCAGT A C FUS Ensembl:ENSG00000089280 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs780643155 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_234604,Human_RBP_ID_4366690,Human_RBP_ID_6509173,Human_RBP_ID_12724309,Human_RBP_ID_22473832,Human_RBP_ID_25244089 RMVar_hsa_circ_10497 27170 RMVar_ID_27170 Human_SNP_ID_599714067 A-to-I Human chr16 + 31193772 31193764 31193772 CTCCCACCTCAGCCTCCCAAGTAGCTGGGACTACAGGTGCTTCCTCGCTACCACACCTGGGTAAT CTCCCACCTCAGCCTCCCAAGTAGC________CAGGTGCTTCCTCGCTACCACACCTGGGTAAT CTGGGACTA C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1189835613 Functional Loss DEL dbSNP153 26..33 33 - - - Human_RBP_ID_6509462 27171 RMVar_ID_27171 Human_SNP_ID_599714069 A-to-I Human chr16 + 31193772 31193766 31193773 CTCCCACCTCAGCCTCCCAAGTAGCTGGGACTACAGGTGCTTCCTCGCTACCACACCTGGGTAAT CTCCCACCTCAGCCTCCCAAGTAGCTG_______AGGTGCTTCCTCGCTACCACACCTGGGTAAT GGGACTAC G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1185107113 Functional Loss DEL dbSNP153 28..34 33 - - - Human_RBP_ID_6509462 27172 RMVar_ID_27172 Human_SNP_ID_599714070 A-to-I Human chr16 + 31193772 31193772 31193772 CTCCCACCTCAGCCTCCCAAGTAGCTGGGACTACAGGTGCTTCCTCGCTACCACACCTGGGTAAT CTCCCACCTCAGCCTCCCAAGTAGCTGGGACTGCAGGTGCTTCCTCGCTACCACACCTGGGTAAT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs774276688 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6509462 27173 RMVar_ID_27173 Human_SNP_ID_599714396 A-to-I Human chr16 + 31194401 31194401 31194401 ACCTCTGCCTCCCACCCGCAAGCTATCTGCCCACCTCAGCCTCTGGAGTAGCTGGGACGGGACTA ACCTCTGCCTCCCACCCGCAAGCTATCTGCCCGCCTCAGCCTCTGGAGTAGCTGGGACGGGACTA A G - - Other Unknown GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1426992975 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6509492,Human_RBP_ID_12724980 27174 RMVar_ID_27174 Human_SNP_ID_599719568 A-to-I Human chr16 + 31210626 31210626 31210626 GGGAGGTCGAGGCTGTAGTGAGCTATGATTATAACATTGCACTCCAGCCTGGGCGACACAGTGAG GGGAGGTCGAGGCTGTAGTGAGCTATGATTATGACATTGCACTCCAGCCTGGGCGACACAGTGAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1194099315 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12725646 27175 RMVar_ID_27175 Human_SNP_ID_599760485 A-to-I Human chr16 + 31362609 31362609 31362609 TGGGGGCCTTTGTGCTGAGGCCTGGGCCCCTCAGGTTACTCCACCGAGCTGGCCCTCTGGAAAGG TGGGGGCCTTTGTGCTGAGGCCTGGGCCCCTCCGGTTACTCCACCGAGCTGGCCCTCTGGAAAGG A C ITGAX Ensembl:ENSG00000140678 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1177322731 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58513,RMVar_hsa_circ_178038,RMVar_hsa_circ_83022,RMVar_hsa_circ_93352,RMVar_hsa_circ_178039,RMVar_hsa_circ_178040,RMVar_hsa_circ_313180 27176 RMVar_ID_27176 Human_SNP_ID_599771152 A-to-I Human chr16 - 31402671 31402671 31402671 TTGAGCCTGGGAGATCAAGTCTGCAGTGAGCTATGATTGCACCCCCACACTGCAGCCTGGATGAC TTGAGCCTGGGAGATCAAGTCTGCAGTGAGCTGTGATTGCACCCCCACACTGCAGCCTGGATGAC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs967034616 Functional Loss SNV dbSNP153 33..33 33 - - - 27177 RMVar_ID_27177 Human_SNP_ID_599784348 A-to-I Human chr16 - 31451228 31451228 31451228 CCAGGATGGTCCTGAACTCCTGGGCTCAAGCAATCCTCCCACCTCAGTCTCCCAAAGTGCTGGGA CCAGGATGGTCCTGAACTCCTGGGCTCAAGCAGTCCTCCCACCTCAGTCTCCCAAAGTGCTGGGA T C AC026471.4 Ensembl:ENSG00000261474 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs765974849 Functional Loss SNV dbSNP153 33..33 33 - - - 27178 RMVar_ID_27178 Human_SNP_ID_599784379 A-to-I Human chr16 - 31451324 31451324 31451324 TCAGCCTCCCAAGTAGCTGGGACTACAGGCATATGCCACCACACCCAGCTAATTTTTAATTTTTT TCAGCCTCCCAAGTAGCTGGGACTACAGGCATGTGCCACCACACCCAGCTAATTTTTAATTTTTT T C AC026471.4 Ensembl:ENSG00000261474 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs998580229 Functional Loss SNV dbSNP153 33..33 33 - - - 27179 RMVar_ID_27179 Human_SNP_ID_599784400 A-to-I Human chr16 - 31451397 31451397 31451397 CAGGCTGGGGTGCAGTGGTGCGACCACAGCCCACTGCAGCCTCGACTTCCTGGGCTCAGGTGATC CAGGCTGGGGTGCAGTGGTGCGACCACAGCCCGCTGCAGCCTCGACTTCCTGGGCTCAGGTGATC T C AC026471.4 Ensembl:ENSG00000261474 lincRNA intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs972179308 Functional Loss SNV dbSNP153 33..33 33 - - - 27180 RMVar_ID_27180 Human_SNP_ID_599784406 A-to-I Human chr16 - 31451428 31451428 31451428 TGGTTTTTTGAGATAGGGTCTCTCCCTCACCCAGGCTGGGGTGCAGTGGTGCGACCACAGCCCAC TGGTTTTTTGAGATAGGGTCTCTCCCTCACCCGGGCTGGGGTGCAGTGGTGCGACCACAGCCCAC T C AC026471.4 Ensembl:ENSG00000261474 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs986570206 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6509897 27181 RMVar_ID_27181 Human_SNP_ID_599784861 A-to-I Human chr16 - 31453227 31453202 31453227 GCTTTGGGAGGCCGAGGTGGGCAGATCACCTGAGGTCAGGAGTTCGAGACCAGGCTGCCCAACGT GCTTTGGGAGGCCGAGGTGGGCAGATCACCTG_________________________CCCAACGT GCAGCCTGGTCTCGAACTCCTGACCT G AC026471.4 Ensembl:ENSG00000261474 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1378671858 Functional Loss DEL dbSNP153 33..57 33 - - - 27182 RMVar_ID_27182 Human_SNP_ID_599784871 A-to-I Human chr16 - 31453222 31453222 31453222 GGGAGGCCGAGGTGGGCAGATCACCTGAGGTCAGGAGTTCGAGACCAGGCTGCCCAACGTGGTGA GGGAGGCCGAGGTGGGCAGATCACCTGAGGTCGGGAGTTCGAGACCAGGCTGCCCAACGTGGTGA T C AC026471.4 Ensembl:ENSG00000261474 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1255019418 Functional Loss SNV dbSNP153 33..33 33 - - - 27183 RMVar_ID_27183 Human_SNP_ID_599785174 A-to-I Human chr16 - 31454201 31454200 31454201 AAGAGGCTGAGGCAAGAGAATGGCATGAACCCAGGAGGCAGAGCTTGCAGTGGGCGGAGATCCTG AAGAGGCTGAGGCAAGAGAATGGCATGAACCC_GGAGGCAGAGCTTGCAGTGGGCGGAGATCCTG CT C - - Other Unknown GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs906192357 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_6509937,Human_RBP_ID_12726340 27184 RMVar_ID_27184 Human_SNP_ID_599785176 A-to-I Human chr16 - 31454205 31454205 31454205 ACTCAAGAGGCTGAGGCAAGAGAATGGCATGAACCCAGGAGGCAGAGCTTGCAGTGGGCGGAGAT ACTCAAGAGGCTGAGGCAAGAGAATGGCATGACCCCAGGAGGCAGAGCTTGCAGTGGGCGGAGAT T G - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs937875499 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6509937,Human_RBP_ID_12726340,Human_RBP_ID_25207712 27185 RMVar_ID_27185 Human_SNP_ID_599785358 A-to-I Human chr16 - 31454764 31454764 31454764 GGGCTCAAGTGATCCTCCCACCTTAACCTCCCAAGGAGCTGGGACTACAGGCATACACCACCACA GGGCTCAAGTGATCCTCCCACCTTAACCTCCCGAGGAGCTGGGACTACAGGCATACACCACCACA T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1334444992 Functional Loss SNV dbSNP153 33..33 33 - - - 27186 RMVar_ID_27186 Human_SNP_ID_599785421 A-to-I Human chr16 - 31454973 31454973 31454973 TTTTGTTGCCCAGGCTGGTCTCTGAAACTTCCAGGCTCAAGCAATCCCCCTGCCTCAGCCTCCCA TTTTGTTGCCCAGGCTGGTCTCTGAAACTTCCGGGCTCAAGCAATCCCCCTGCCTCAGCCTCCCA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049791539 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12726356,Human_RBP_ID_23164070,Human_RBP_ID_23687763 27187 RMVar_ID_27187 Human_SNP_ID_599786239 A-to-I Human chr16 - 31457600 31457600 31457600 AAAAATGCTAGGCGTGTTGGCTCTCGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAC AAAAATGCTAGGCGTGTTGGCTCTCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAC T C AC026471.1 Ensembl:ENSG00000260267 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991949985 Functional Loss SNV dbSNP153 33..33 33 - - - 27188 RMVar_ID_27188 Human_SNP_ID_599816276 A-to-I Human chr16 - 31568628 31568628 31568628 TCATCGAAATCCAACTTACCGCCCAAGGTACCATAGCAGGGGACCTCCTCGCCCACGACCTGCCC TCATCGAAATCCAACTTACCGCCCAAGGTACCGTAGCAGGGGACCTCCTCGCCCACGACCTGCCC T C YBX3P1 Ensembl:ENSG00000261614 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879008997 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5573403,Human_RBP_ID_6550223,Human_RBP_ID_22389033 Human_miRNA_ID_1829951 27189 RMVar_ID_27189 Human_SNP_ID_599816375 A-to-I Human chr16 - 31568945 31568945 31568945 CCGTTACAGACGTGGCTACTATGGAAGGCGCCATGGCCCTCCCCGGGATTACGCTGGGAGGAGGA CCGTTACAGACGTGGCTACTATGGAAGGCGCCTTGGCCCTCCCCGGGATTACGCTGGGAGGAGGA T A YBX3P1 Ensembl:ENSG00000261614 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968989121 Functional Loss SNV dbSNP153 33..33 33 - - - 27190 RMVar_ID_27190 Human_SNP_ID_599816376 A-to-I Human chr16 - 31568945 31568945 31568945 CCGTTACAGACGTGGCTACTATGGAAGGCGCCATGGCCCTCCCCGGGATTACGCTGGGAGGAGGA CCGTTACAGACGTGGCTACTATGGAAGGCGCCGTGGCCCTCCCCGGGATTACGCTGGGAGGAGGA T C YBX3P1 Ensembl:ENSG00000261614 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968989121 Functional Loss SNV dbSNP153 33..33 33 - - - 27191 RMVar_ID_27191 Human_SNP_ID_599816473 A-to-I Human chr16 - 31569164 31569164 31569164 ATGGATATGGATTTATAAATCGAAATGACACCAAAGAAGATCTATTTATACATCAGACTGCCATC ATGGATATGGATTTATAAATCGAAATGACACCGAAGAAGATCTATTTATACATCAGACTGCCATC T C YBX3P1 Ensembl:ENSG00000261614 Pseudogene exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1319562105 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1841915,Human_RBP_ID_4399885,Human_RBP_ID_5096648,Human_RBP_ID_5573405,Human_RBP_ID_17373180,Human_RBP_ID_18285421,Human_RBP_ID_18678575,Human_RBP_ID_22939073,Human_RBP_ID_26441010 Human_miRNA_ID_1852329,Human_miRNA_ID_1854401,Human_miRNA_ID_1911484 27192 RMVar_ID_27192 Human_SNP_ID_599870918 A-to-I Human chr16 + 31806327 31806327 31806327 ATACACACTGGATCATATAAGAGCCCTGGGTCATTTACAAGAAGTTCCACATGAGGGCCCAATGT ATACACACTGGATCATATAAGAGCCCTGGGTCGTTTACAAGAAGTTCCACATGAGGGCCCAATGT A G AC002519.2 Ensembl:ENSG00000261457 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs986212850 Functional Loss SNV dbSNP153 33..33 33 - - - 27193 RMVar_ID_27193 Human_SNP_ID_599870919 A-to-I Human chr16 + 31806333 31806333 31806333 ACTGGATCATATAAGAGCCCTGGGTCATTTACAAGAAGTTCCACATGAGGGCCCAATGTATGATC ACTGGATCATATAAGAGCCCTGGGTCATTTACGAGAAGTTCCACATGAGGGCCCAATGTATGATC A G AC002519.2 Ensembl:ENSG00000261457 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1451752698 Functional Loss SNV dbSNP153 33..33 33 - - - 27194 RMVar_ID_27194 Human_SNP_ID_599870929 A-to-I Human chr16 + 31806360 31806360 31806360 TTTACAAGAAGTTCCACATGAGGGCCCAATGTATGATCTATTACGGTCAGATCCAGATGATCGTG TTTACAAGAAGTTCCACATGAGGGCCCAATGTGTGATCTATTACGGTCAGATCCAGATGATCGTG A G AC002519.2 Ensembl:ENSG00000261457 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1191085795 Functional Loss SNV dbSNP153 33..33 33 - - - 27195 RMVar_ID_27195 Human_SNP_ID_599870932 A-to-I Human chr16 + 31806367 31806367 31806367 GAAGTTCCACATGAGGGCCCAATGTATGATCTATTACGGTCAGATCCAGATGATCGTGGTGGATG GAAGTTCCACATGAGGGCCCAATGTATGATCTGTTACGGTCAGATCCAGATGATCGTGGTGGATG A G AC002519.2 Ensembl:ENSG00000261457 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1249114105 Functional Loss SNV dbSNP153 33..33 33 - - - 27196 RMVar_ID_27196 Human_SNP_ID_600419439 A-to-I Human chr16 - 34093265 34093265 34093265 ATCATCGAATGGAAATGAATGGAATCATCATCAAATGGAAATGAATGGAATCATTGAATGGAATC ATCATCGAATGGAAATGAATGGAATCATCATCGAATGGAAATGAATGGAATCATTGAATGGAATC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs149614278 Functional Loss SNV dbSNP153 33..33 33 - - - 27197 RMVar_ID_27197 Human_SNP_ID_600419452 A-to-I Human chr16 - 34093290 34093290 34093290 TCATCGAATGAAATCGAATGGAATCATCATCGAATGGAAATGAATGGAATCATCATCAAATGGAA TCATCGAATGAAATCGAATGGAATCATCATCGGATGGAAATGAATGGAATCATCATCAAATGGAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs182587073 Functional Loss SNV dbSNP153 33..33 33 - - - 27198 RMVar_ID_27198 Human_SNP_ID_600419459 A-to-I Human chr16 - 34093297 34093297 34093297 AATGGAATCATCGAATGAAATCGAATGGAATCATCATCGAATGGAAATGAATGGAATCATCATCA AATGGAATCATCGAATGAAATCGAATGGAATCGTCATCGAATGGAAATGAATGGAATCATCATCA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1206757274 Functional Loss SNV dbSNP153 33..33 33 - - - 27199 RMVar_ID_27199 Human_SNP_ID_718722172 A-to-I Human chrX - 63504367 63504367 63504367 AAATTAGCCGGGTGTGGTGGCACGTGCCTGTAATCCCAGCTATGTGGGGGTCTGAGGCAGGAGAA AAATTAGCCGGGTGTGGTGGCACGTGCCTGTAGTCCCAGCTATGTGGGGGTCTGAGGCAGGAGAA T C LINC01278 Ensembl:ENSG00000235437 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1490149468 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98838,RMVar_hsa_circ_262693 27200 RMVar_ID_27200 Human_SNP_ID_718732969 A-to-I Human chrX - 63545895 63545895 63545895 TAACATTGACTCTGTAAATTGGTTAGGACACTATGGCCATTTTGACAATATTGATTATTCCTTTC TAACATTGACTCTGTAAATTGGTTAGGACACTGTGGCCATTTTGACAATATTGATTATTCCTTTC T C LINC01278 Ensembl:ENSG00000235437 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1556195401 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98838,RMVar_hsa_circ_262693 27201 RMVar_ID_27201 Human_SNP_ID_718735801 A-to-I Human chrX - 63558199 63558199 63558199 TTCTTCTGCTTTTTTTGAAATGTACAATAAATAGTTGTTAACTATTAGTGGCCCTATTGTACTAC TTCTTCTGCTTTTTTTGAAATGTACAATAAATGGTTGTTAACTATTAGTGGCCCTATTGTACTAC T C LINC01278 Ensembl:ENSG00000235437 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1315972447 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8720952 RMVar_hsa_circ_98838,RMVar_hsa_circ_262693 27202 RMVar_ID_27202 Human_SNP_ID_718775161 A-to-I Human chrX - 63749329 63749329 63749329 TACTTGGGAGGCTGAGGCAGGAGAGTCACTTGAACCCAGGAGGCGGAGGATGCAGTGAGCCGAGA TACTTGGGAGGCTGAGGCAGGAGAGTCACTTGGACCCAGGAGGCGGAGGATGCAGTGAGCCGAGA T C ARHGEF9 Ensembl:ENSG00000131089 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs188185859 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_536,RMVar_hsa_circ_106322,RMVar_hsa_circ_262696,RMVar_hsa_circ_13386,RMVar_hsa_circ_262712,RMVar_hsa_circ_43951 27203 RMVar_ID_27203 Human_SNP_ID_719295772 A-to-I Human chrX + 65727912 65727912 65727912 TTCTCCACCTGGCTGAAACTCAATAAGAAGGTAACTGCTTATTCCTCTGTTGGATTTAGAATTCT TTCTCCACCTGGCTGAAACTCAATAAGAAGGTGACTGCTTATTCCTCTGTTGGATTTAGAATTCT A G MSN Ensembl:ENSG00000147065 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs977193697 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2213111,Human_Splice_Rec_2213133 RMVar_hsa_circ_40509,RMVar_hsa_circ_104004,RMVar_hsa_circ_128107,RMVar_hsa_circ_370597,RMVar_hsa_circ_112857,RMVar_hsa_circ_107842,RMVar_hsa_circ_262753,RMVar_hsa_circ_262757,RMVar_hsa_circ_91745,RMVar_hsa_circ_262758,RMVar_hsa_circ_262755,RMVar_hsa_circ_262756,RMVar_hsa_circ_262754,RMVar_hsa_circ_124391,RMVar_hsa_circ_51167,RMVar_hsa_circ_262762 27204 RMVar_ID_27204 Human_SNP_ID_719499952 A-to-I Human chrX + 66497804 66497803 66497804 AGTCAGTGCCGGAGGACCTCAGCAGCCATGTCAAAGCCCCATAGTGAAGCCAAGACTGCTTTCAT AGTCAGTGCCGGAGGACCTCAGCAGCCATGTC_AAGCCCCATAGTGAAGCCAAGACTGCTTTCAT CA C PKMP2 Ensembl:ENSG00000235892 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1320224687 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5108137,Human_RBP_ID_8277385,Human_RBP_ID_18543619 27205 RMVar_ID_27205 Human_SNP_ID_719928183 A-to-I Human chrX - 68070574 68070574 68070574 AGACATGTGAGCACTACGGGTGGTGCCAGTTTAGAGCTCCTGGACAGTAAAGTCCTTCCTGGGGT AGACATGTGAGCACTACGGGTGGTGCCAGTTTGGAGCTCCTGGACAGTAAAGTCCTTCCTGGGGT T C AL158201.1,OPHN1 Ensembl:ENSG00000228328,Ensembl:ENSG00000079482 Pseudogene,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879228606 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89329,RMVar_hsa_circ_262797,RMVar_hsa_circ_125754,RMVar_hsa_circ_262799,RMVar_hsa_circ_378257,RMVar_hsa_circ_262800,RMVar_hsa_circ_343911,RMVar_hsa_circ_293079,RMVar_hsa_circ_294332,RMVar_hsa_circ_345613,RMVar_hsa_circ_289141,RMVar_hsa_circ_262805,RMVar_hsa_circ_36151,RMVar_hsa_circ_39994,RMVar_hsa_circ_262806,RMVar_hsa_circ_262807,RMVar_hsa_circ_262804 27206 RMVar_ID_27206 Human_SNP_ID_719928191 A-to-I Human chrX - 68070604 68070604 68070604 TGTGCCAAATGGAACACAGAGGATAAAATCAGACATGTGAGCACTACGGGTGGTGCCAGTTTAGA TGTGCCAAATGGAACACAGAGGATAAAATCAGCCATGTGAGCACTACGGGTGGTGCCAGTTTAGA T G AL158201.1,OPHN1 Ensembl:ENSG00000228328,Ensembl:ENSG00000079482 Pseudogene,Protein coding exon,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs879182516 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89329,RMVar_hsa_circ_262797,RMVar_hsa_circ_125754,RMVar_hsa_circ_262799,RMVar_hsa_circ_378257,RMVar_hsa_circ_262800,RMVar_hsa_circ_343911,RMVar_hsa_circ_293079,RMVar_hsa_circ_294332,RMVar_hsa_circ_345613,RMVar_hsa_circ_289141,RMVar_hsa_circ_262805,RMVar_hsa_circ_36151,RMVar_hsa_circ_39994,RMVar_hsa_circ_262806,RMVar_hsa_circ_262807,RMVar_hsa_circ_262804 27207 RMVar_ID_27207 Human_SNP_ID_719928192 A-to-I Human chrX - 68070609 68070609 68070609 CTTGCTGTGCCAAATGGAACACAGAGGATAAAATCAGACATGTGAGCACTACGGGTGGTGCCAGT CTTGCTGTGCCAAATGGAACACAGAGGATAAAGTCAGACATGTGAGCACTACGGGTGGTGCCAGT T C AL158201.1,OPHN1 Ensembl:ENSG00000228328,Ensembl:ENSG00000079482 Pseudogene,Protein coding exon,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs879104289 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89329,RMVar_hsa_circ_262797,RMVar_hsa_circ_125754,RMVar_hsa_circ_262799,RMVar_hsa_circ_378257,RMVar_hsa_circ_262800,RMVar_hsa_circ_343911,RMVar_hsa_circ_293079,RMVar_hsa_circ_294332,RMVar_hsa_circ_345613,RMVar_hsa_circ_289141,RMVar_hsa_circ_262805,RMVar_hsa_circ_36151,RMVar_hsa_circ_39994,RMVar_hsa_circ_262806,RMVar_hsa_circ_262807,RMVar_hsa_circ_262804 27208 RMVar_ID_27208 Human_SNP_ID_719928199 A-to-I Human chrX - 68070651 68070651 68070651 CTAGGGGCTGCATTACCATCATAGGTGGTGGAAACACTGCCACTTGCTGTGCCAAATGGAACACA CTAGGGGCTGCATTACCATCATAGGTGGTGGAGACACTGCCACTTGCTGTGCCAAATGGAACACA T C AL158201.1,OPHN1 Ensembl:ENSG00000228328,Ensembl:ENSG00000079482 Pseudogene,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879164909 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22413407 Human_miRNA_ID_1860718,Human_miRNA_ID_1861162,Human_miRNA_ID_1875221,Human_miRNA_ID_1875501 RMVar_hsa_circ_89329,RMVar_hsa_circ_262797,RMVar_hsa_circ_125754,RMVar_hsa_circ_262799,RMVar_hsa_circ_378257,RMVar_hsa_circ_262800,RMVar_hsa_circ_343911,RMVar_hsa_circ_293079,RMVar_hsa_circ_294332,RMVar_hsa_circ_345613,RMVar_hsa_circ_289141,RMVar_hsa_circ_262805,RMVar_hsa_circ_36151,RMVar_hsa_circ_39994,RMVar_hsa_circ_262806,RMVar_hsa_circ_262807,RMVar_hsa_circ_262804 27209 RMVar_ID_27209 Human_SNP_ID_719951175 A-to-I Human chrX - 68208219 68208219 68208219 GGATGTGGTGATGCTTGCCTGTAATCCTAGCTACTTGGGAGGCTGAGGCAGGGGAATGACTTGAA GGATGTGGTGATGCTTGCCTGTAATCCTAGCTGCTTGGGAGGCTGAGGCAGGGGAATGACTTGAA T C OPHN1 Ensembl:ENSG00000079482 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749876892 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26286243 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 27210 RMVar_ID_27210 Human_SNP_ID_719975033 A-to-I Human chrX - 68339743 68339743 68339743 TAAAAATTAGCTGGGCACGGTGGCACATGCCTATAATTCCAGCTACCTGGGAGGCTGAAGCACGA TAAAAATTAGCTGGGCACGGTGGCACATGCCTGTAATTCCAGCTACCTGGGAGGCTGAAGCACGA T C OPHN1 Ensembl:ENSG00000079482 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs993515502 Functional Loss SNV dbSNP153 33..33 33 - - - 27211 RMVar_ID_27211 Human_SNP_ID_720005684 A-to-I Human chrX + 68513590 68513590 68513590 CAGAAATTAAAAATTGATTTTATTTTATTTTTATTTTCATTTTTTTTTGAGACAGAGTCTCACTC CAGAAATTAAAAATTGATTTTATTTTATTTTTTTTTTCATTTTTTTTTGAGACAGAGTCTCACTC A T YIPF6 Ensembl:ENSG00000181704 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1220833772 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7754,RMVar_hsa_circ_273032,RMVar_hsa_circ_262834,RMVar_hsa_circ_314302,RMVar_hsa_circ_262833,RMVar_hsa_circ_283997 27212 RMVar_ID_27212 Human_SNP_ID_720005708 A-to-I Human chrX + 68513717 68513717 68513717 TCAAGTAATTTTCATGCCTCAGCCTCCTGAGTAGCTGGGATTAAAGGCGCCCACCACCATGCCCA TCAAGTAATTTTCATGCCTCAGCCTCCTGAGTTGCTGGGATTAAAGGCGCCCACCACCATGCCCA A T YIPF6 Ensembl:ENSG00000181704 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017485395 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7754,RMVar_hsa_circ_273032,RMVar_hsa_circ_262834,RMVar_hsa_circ_314302,RMVar_hsa_circ_262833,RMVar_hsa_circ_283997 27213 RMVar_ID_27213 Human_SNP_ID_720005719 A-to-I Human chrX + 68513786 68513786 68513786 ATTTTTTTGTATTTTTAGTAGAGACGGATTTCACCAGGTTGGCCAGGCTGGTTTCCAACTCCCGA ATTTTTTTGTATTTTTAGTAGAGACGGATTTCGCCAGGTTGGCCAGGCTGGTTTCCAACTCCCGA A G YIPF6 Ensembl:ENSG00000181704 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1468298828 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7754,RMVar_hsa_circ_273032,RMVar_hsa_circ_262834,RMVar_hsa_circ_314302,RMVar_hsa_circ_262833,RMVar_hsa_circ_283997 27214 RMVar_ID_27214 Human_SNP_ID_720005882 A-to-I Human chrX + 68514609 68514609 68514609 TTTTTGTGTTGTTAGTAGAGACGGGTTTTGCCATGTTGGCCAGGCTGGTCTCGAACTGCTGACCT TTTTTGTGTTGTTAGTAGAGACGGGTTTTGCCGTGTTGGCCAGGCTGGTCTCGAACTGCTGACCT A G YIPF6 Ensembl:ENSG00000181704 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs914032764 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7754,RMVar_hsa_circ_273032,RMVar_hsa_circ_262834,RMVar_hsa_circ_314302,RMVar_hsa_circ_262833,RMVar_hsa_circ_283997 27215 RMVar_ID_27215 Human_SNP_ID_720149591 A-to-I Human chrX + 69287970 69287970 69287970 GTGGTGGTGCATGCCTGTGGTCCCAGCTGCTCAGGAGGCTGAGGTGGGAGGATCACCTGGGCCCA GTGGTGGTGCATGCCTGTGGTCCCAGCTGCTCGGGAGGCTGAGGTGGGAGGATCACCTGGGCCCA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1296708706 Functional Loss SNV dbSNP153 33..33 33 - - - 27216 RMVar_ID_27216 Human_SNP_ID_720245856 A-to-I Human chrX + 69810042 69810042 69810042 CCAGCACTTTGGGGGGCTGAGGTGGGCGGATCACGAGGTCAGGAGTTCGAGACCAGCCTGACCAA CCAGCACTTTGGGGGGCTGAGGTGGGCGGATCGCGAGGTCAGGAGTTCGAGACCAGCCTGACCAA A G EDA Ensembl:ENSG00000158813 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs777234782 Functional Loss SNV dbSNP153 33..33 33 - - - 27217 RMVar_ID_27217 Human_SNP_ID_720301361 A-to-I Human chrX + 70142077 70142077 70142077 AGAGTAGGCCAGGTGTGGTGGCTCATTCCTGCAATCCCAGCACTTTGGGAGGACAAGGCGGGCAG AGAGTAGGCCAGGTGTGGTGGCTCATTCCTGCCATCCCAGCACTTTGGGAGGACAAGGCGGGCAG A C IGBP1 Ensembl:ENSG00000089289 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs766189492 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77551,RMVar_hsa_circ_262844 27218 RMVar_ID_27218 Human_SNP_ID_720301741 A-to-I Human chrX + 70143928 70143928 70143928 AAAGATGATGAGCAGGCTGGGCGCGGTGGCTCACGCCTGGAACGCACTTTGAGAGGCTAAGGCAG AAAGATGATGAGCAGGCTGGGCGCGGTGGCTCCCGCCTGGAACGCACTTTGAGAGGCTAAGGCAG A C IGBP1 Ensembl:ENSG00000089289 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs758759333 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77551,RMVar_hsa_circ_262844 27219 RMVar_ID_27219 Human_SNP_ID_720429035 A-to-I Human chrX + 70857601 70857601 70857601 GATATGTCATATATCTCAAAATGGTTCAAGTGAGTGTACCAGTGATGGCAATAAGAAAAATGATA GATATGTCATATATCTCAAAATGGTTCAAGTGGGTGTACCAGTGATGGCAATAAGAAAAATGATA A G - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1191033548 Functional Loss SNV dbSNP153 33..33 33 - - - 27220 RMVar_ID_27220 Human_SNP_ID_720463389 A-to-I Human chrX - 71047074 71047074 71047074 TTGTCCAGACTGGTCTTGAACTCCTGGGCTCTAGTGATCCTCTCACCTCAGCCTCCTGAAGTCTT TTGTCCAGACTGGTCTTGAACTCCTGGGCTCTGGTGATCCTCTCACCTCAGCCTCCTGAAGTCTT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs781770611 Functional Loss SNV dbSNP153 33..33 33 - - - 27221 RMVar_ID_27221 Human_SNP_ID_720503735 A-to-I Human chrX + 71258158 71258158 71258158 CCACCACACCAGCTAATTTTTGTATTTTTTTTAGTACAGATGGGTTCCACCATGTTGGCTATGGT CCACCACACCAGCTAATTTTTGTATTTTTTTTGGTACAGATGGGTTCCACCATGTTGGCTATGGT A G RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1261166186 Functional Loss SNV dbSNP153 33..33 33 - - - 27222 RMVar_ID_27222 Human_SNP_ID_720509997 A-to-I Human chrX + 71292432 71292432 71292432 TTTGGCCAGGCTGGTCTCGAGCTCCTGACCTCAGGAGATCCACCCACCTTGGCCTCCCAAAGTAT TTTGGCCAGGCTGGTCTCGAGCTCCTGACCTCGGGAGATCCACCCACCTTGGCCTCCCAAAGTAT A G NONO Ensembl:ENSG00000147140 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1222935159 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118976,RMVar_hsa_circ_318066,RMVar_hsa_circ_262912 27223 RMVar_ID_27223 Human_SNP_ID_720510621 A-to-I Human chrX + 71295551 71295551 71295551 ATGGTGGCTCATGCCTGTAATACCAACACTTCAGGAGGCTGAGGCGGGTGAATCACGAGGTCCTG ATGGTGGCTCATGCCTGTAATACCAACACTTCGGGAGGCTGAGGCGGGTGAATCACGAGGTCCTG A G NONO Ensembl:ENSG00000147140 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928976876 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118976,RMVar_hsa_circ_125489,RMVar_hsa_circ_262912,RMVar_hsa_circ_114603,RMVar_hsa_circ_262913,RMVar_hsa_circ_262914 27224 RMVar_ID_27224 Human_SNP_ID_720514673 A-to-I Human chrX - 71315220 71315220 71315220 TGATAAATCCAAGTGTTATGAATGTGGGGAAAATGGACACTTAAGTTATGCCTGTCCGAAAAATA TGATAAATCCAAGTGTTATGAATGTGGGGAAAGTGGACACTTAAGTTATGCCTGTCCGAAAAATA T C AL590762.3 Ensembl:ENSG00000224208 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270542992 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8277285,Human_RBP_ID_17718656 27225 RMVar_ID_27225 Human_SNP_ID_720516845 A-to-I Human chrX + 71327340 71327340 71327340 AATCCCCATCTGTACTAAAAATACAAAAAATTAGCTGGACGTGGTGGTGAGTGCCTGTAGTTTCA AATCCCCATCTGTACTAAAAATACAAAAAATTGGCTGGACGTGGTGGTGAGTGCCTGTAGTTTCA A G RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1307253072 Functional Loss SNV dbSNP153 33..33 33 - - - 27226 RMVar_ID_27226 Human_SNP_ID_720525183 A-to-I Human chrX + 71370416 71370416 71370416 TCACCAGGGCTGGAGTGCAGTGGTGTGATCTCAGCTCACTGCAACTTCCACCTACCGGGTTCAAG TCACCAGGGCTGGAGTGCAGTGGTGTGATCTCGGCTCACTGCAACTTCCACCTACCGGGTTCAAG A G TAF1 Ensembl:ENSG00000147133 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1462117891 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64295,RMVar_hsa_circ_351429,RMVar_hsa_circ_355603,RMVar_hsa_circ_352418,RMVar_hsa_circ_85953,RMVar_hsa_circ_329396,RMVar_hsa_circ_69803,RMVar_hsa_circ_53445,RMVar_hsa_circ_63682,RMVar_hsa_circ_45492,RMVar_hsa_circ_262927,RMVar_hsa_circ_274652,RMVar_hsa_circ_262925,RMVar_hsa_circ_262926,RMVar_hsa_circ_302512,RMVar_hsa_circ_325172,RMVar_hsa_circ_363913,RMVar_hsa_circ_279834,RMVar_hsa_circ_75437,RMVar_hsa_circ_104665,RMVar_hsa_circ_262929,RMVar_hsa_circ_262930,RMVar_hsa_circ_262928 27227 RMVar_ID_27227 Human_SNP_ID_720530369 A-to-I Human chrX + 71396896 71396896 71396896 CTCTACAAAAATTTAGCTGGGTGTGGTGGTACACGCCTGTAGTCCCAGCTACTCAGAAGGCTGAG CTCTACAAAAATTTAGCTGGGTGTGGTGGTACCCGCCTGTAGTCCCAGCTACTCAGAAGGCTGAG A C TAF1 Ensembl:ENSG00000147133 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs556254718 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64295,RMVar_hsa_circ_351429,RMVar_hsa_circ_355603,RMVar_hsa_circ_352418,RMVar_hsa_circ_329396,RMVar_hsa_circ_45492,RMVar_hsa_circ_262926,RMVar_hsa_circ_302512,RMVar_hsa_circ_325172,RMVar_hsa_circ_75437,RMVar_hsa_circ_104665,RMVar_hsa_circ_262929,RMVar_hsa_circ_262930,RMVar_hsa_circ_62329,RMVar_hsa_circ_19464,RMVar_hsa_circ_374581,RMVar_hsa_circ_337595,RMVar_hsa_circ_295602,RMVar_hsa_circ_116322,RMVar_hsa_circ_56397,RMVar_hsa_circ_262934,RMVar_hsa_circ_262935,RMVar_hsa_circ_48654,RMVar_hsa_circ_360105,RMVar_hsa_circ_366135,RMVar_hsa_circ_33065,RMVar_hsa_circ_48829,RMVar_hsa_circ_29000,RMVar_hsa_circ_21188,RMVar_hsa_circ_90821,RMVar_hsa_circ_262938,RMVar_hsa_circ_350953,RMVar_hsa_circ_67237 27228 RMVar_ID_27228 Human_SNP_ID_720530511 A-to-I Human chrX + 71397593 71397593 71397593 CAACCTCCATCTCTCAGGTTCAAGTGATTCTCATGCCTCAACTTCCAGAGTAGCTGGGATTACAG CAACCTCCATCTCTCAGGTTCAAGTGATTCTCCTGCCTCAACTTCCAGAGTAGCTGGGATTACAG A C TAF1 Ensembl:ENSG00000147133 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs5980760 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2778 RMVar_hsa_circ_64295,RMVar_hsa_circ_351429,RMVar_hsa_circ_355603,RMVar_hsa_circ_352418,RMVar_hsa_circ_329396,RMVar_hsa_circ_45492,RMVar_hsa_circ_262926,RMVar_hsa_circ_302512,RMVar_hsa_circ_325172,RMVar_hsa_circ_75437,RMVar_hsa_circ_104665,RMVar_hsa_circ_262929,RMVar_hsa_circ_262930,RMVar_hsa_circ_62329,RMVar_hsa_circ_19464,RMVar_hsa_circ_374581,RMVar_hsa_circ_337595,RMVar_hsa_circ_295602,RMVar_hsa_circ_116322,RMVar_hsa_circ_56397,RMVar_hsa_circ_262934,RMVar_hsa_circ_262935,RMVar_hsa_circ_48654,RMVar_hsa_circ_360105,RMVar_hsa_circ_366135,RMVar_hsa_circ_48829,RMVar_hsa_circ_29000,RMVar_hsa_circ_21188,RMVar_hsa_circ_90821,RMVar_hsa_circ_262938,RMVar_hsa_circ_350953,RMVar_hsa_circ_67237,RMVar_hsa_circ_282933,RMVar_hsa_circ_321330,RMVar_hsa_circ_324027,RMVar_hsa_circ_355198,RMVar_hsa_circ_296888,RMVar_hsa_circ_32131,RMVar_hsa_circ_70132,RMVar_hsa_circ_262939,RMVar_hsa_circ_262940 27229 RMVar_ID_27229 Human_SNP_ID_720530512 A-to-I Human chrX + 71397593 71397593 71397593 CAACCTCCATCTCTCAGGTTCAAGTGATTCTCATGCCTCAACTTCCAGAGTAGCTGGGATTACAG CAACCTCCATCTCTCAGGTTCAAGTGATTCTCGTGCCTCAACTTCCAGAGTAGCTGGGATTACAG A G TAF1 Ensembl:ENSG00000147133 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs5980760 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2778 RMVar_hsa_circ_64295,RMVar_hsa_circ_351429,RMVar_hsa_circ_355603,RMVar_hsa_circ_352418,RMVar_hsa_circ_329396,RMVar_hsa_circ_45492,RMVar_hsa_circ_262926,RMVar_hsa_circ_302512,RMVar_hsa_circ_325172,RMVar_hsa_circ_75437,RMVar_hsa_circ_104665,RMVar_hsa_circ_262929,RMVar_hsa_circ_262930,RMVar_hsa_circ_62329,RMVar_hsa_circ_19464,RMVar_hsa_circ_374581,RMVar_hsa_circ_337595,RMVar_hsa_circ_295602,RMVar_hsa_circ_116322,RMVar_hsa_circ_56397,RMVar_hsa_circ_262934,RMVar_hsa_circ_262935,RMVar_hsa_circ_48654,RMVar_hsa_circ_360105,RMVar_hsa_circ_366135,RMVar_hsa_circ_48829,RMVar_hsa_circ_29000,RMVar_hsa_circ_21188,RMVar_hsa_circ_90821,RMVar_hsa_circ_262938,RMVar_hsa_circ_350953,RMVar_hsa_circ_67237,RMVar_hsa_circ_282933,RMVar_hsa_circ_321330,RMVar_hsa_circ_324027,RMVar_hsa_circ_355198,RMVar_hsa_circ_296888,RMVar_hsa_circ_32131,RMVar_hsa_circ_70132,RMVar_hsa_circ_262939,RMVar_hsa_circ_262940 27230 RMVar_ID_27230 Human_SNP_ID_720530513 A-to-I Human chrX + 71397593 71397593 71397593 CAACCTCCATCTCTCAGGTTCAAGTGATTCTCATGCCTCAACTTCCAGAGTAGCTGGGATTACAG CAACCTCCATCTCTCAGGTTCAAGTGATTCTCTTGCCTCAACTTCCAGAGTAGCTGGGATTACAG A T TAF1 Ensembl:ENSG00000147133 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs5980760 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2778 RMVar_hsa_circ_64295,RMVar_hsa_circ_351429,RMVar_hsa_circ_355603,RMVar_hsa_circ_352418,RMVar_hsa_circ_329396,RMVar_hsa_circ_45492,RMVar_hsa_circ_262926,RMVar_hsa_circ_302512,RMVar_hsa_circ_325172,RMVar_hsa_circ_75437,RMVar_hsa_circ_104665,RMVar_hsa_circ_262929,RMVar_hsa_circ_262930,RMVar_hsa_circ_62329,RMVar_hsa_circ_19464,RMVar_hsa_circ_374581,RMVar_hsa_circ_337595,RMVar_hsa_circ_295602,RMVar_hsa_circ_116322,RMVar_hsa_circ_56397,RMVar_hsa_circ_262934,RMVar_hsa_circ_262935,RMVar_hsa_circ_48654,RMVar_hsa_circ_360105,RMVar_hsa_circ_366135,RMVar_hsa_circ_48829,RMVar_hsa_circ_29000,RMVar_hsa_circ_21188,RMVar_hsa_circ_90821,RMVar_hsa_circ_262938,RMVar_hsa_circ_350953,RMVar_hsa_circ_67237,RMVar_hsa_circ_282933,RMVar_hsa_circ_321330,RMVar_hsa_circ_324027,RMVar_hsa_circ_355198,RMVar_hsa_circ_296888,RMVar_hsa_circ_32131,RMVar_hsa_circ_70132,RMVar_hsa_circ_262939,RMVar_hsa_circ_262940 27231 RMVar_ID_27231 Human_SNP_ID_720530528 A-to-I Human chrX + 71397683 71397683 71397683 TTTTGTATTTTTGGTAGAGATGGGGTTTTGCCATGTTGACCAGGCTGGTGTTGAACTCCTGGGCT TTTTGTATTTTTGGTAGAGATGGGGTTTTGCCGTGTTGACCAGGCTGGTGTTGAACTCCTGGGCT A G TAF1 Ensembl:ENSG00000147133 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1270577572 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64295,RMVar_hsa_circ_351429,RMVar_hsa_circ_355603,RMVar_hsa_circ_352418,RMVar_hsa_circ_329396,RMVar_hsa_circ_45492,RMVar_hsa_circ_262926,RMVar_hsa_circ_302512,RMVar_hsa_circ_325172,RMVar_hsa_circ_75437,RMVar_hsa_circ_104665,RMVar_hsa_circ_262929,RMVar_hsa_circ_262930,RMVar_hsa_circ_62329,RMVar_hsa_circ_19464,RMVar_hsa_circ_374581,RMVar_hsa_circ_337595,RMVar_hsa_circ_295602,RMVar_hsa_circ_116322,RMVar_hsa_circ_56397,RMVar_hsa_circ_262934,RMVar_hsa_circ_262935,RMVar_hsa_circ_48654,RMVar_hsa_circ_360105,RMVar_hsa_circ_366135,RMVar_hsa_circ_48829,RMVar_hsa_circ_29000,RMVar_hsa_circ_21188,RMVar_hsa_circ_90821,RMVar_hsa_circ_262938,RMVar_hsa_circ_350953,RMVar_hsa_circ_67237,RMVar_hsa_circ_282933,RMVar_hsa_circ_321330,RMVar_hsa_circ_324027,RMVar_hsa_circ_355198,RMVar_hsa_circ_296888,RMVar_hsa_circ_32131,RMVar_hsa_circ_70132,RMVar_hsa_circ_262939,RMVar_hsa_circ_262940 27232 RMVar_ID_27232 Human_SNP_ID_720532663 A-to-I Human chrX + 71408416 71408416 71408416 CTTGGCTCACTGCAACCTCCGCCTCTCGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGC CTTGGCTCACTGCAACCTCCGCCTCTCGGTTCCAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGC A C TAF1 Ensembl:ENSG00000147133 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1173946033 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64295,RMVar_hsa_circ_355603,RMVar_hsa_circ_329396,RMVar_hsa_circ_302512,RMVar_hsa_circ_75437,RMVar_hsa_circ_104665,RMVar_hsa_circ_262929,RMVar_hsa_circ_262930,RMVar_hsa_circ_62329,RMVar_hsa_circ_374581,RMVar_hsa_circ_337595,RMVar_hsa_circ_295602,RMVar_hsa_circ_262935,RMVar_hsa_circ_29000,RMVar_hsa_circ_21188,RMVar_hsa_circ_90821,RMVar_hsa_circ_262938,RMVar_hsa_circ_67237,RMVar_hsa_circ_282933,RMVar_hsa_circ_32131,RMVar_hsa_circ_36045,RMVar_hsa_circ_5407,RMVar_hsa_circ_8206,RMVar_hsa_circ_14702 27233 RMVar_ID_27233 Human_SNP_ID_720532682 A-to-I Human chrX + 71408558 71408558 71408558 AGGCTTGTCTCTAACTCCTGACTTCGTCATCCACCCGCCTCAGCCTCCCAGGATTACAGGTGTGA AGGCTTGTCTCTAACTCCTGACTTCGTCATCCCCCCGCCTCAGCCTCCCAGGATTACAGGTGTGA A C TAF1 Ensembl:ENSG00000147133 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991648823 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17579929 RMVar_hsa_circ_64295,RMVar_hsa_circ_355603,RMVar_hsa_circ_329396,RMVar_hsa_circ_302512,RMVar_hsa_circ_75437,RMVar_hsa_circ_104665,RMVar_hsa_circ_262929,RMVar_hsa_circ_262930,RMVar_hsa_circ_62329,RMVar_hsa_circ_374581,RMVar_hsa_circ_337595,RMVar_hsa_circ_295602,RMVar_hsa_circ_262935,RMVar_hsa_circ_29000,RMVar_hsa_circ_21188,RMVar_hsa_circ_90821,RMVar_hsa_circ_262938,RMVar_hsa_circ_67237,RMVar_hsa_circ_282933,RMVar_hsa_circ_32131,RMVar_hsa_circ_36045,RMVar_hsa_circ_5407,RMVar_hsa_circ_8206,RMVar_hsa_circ_14702 27234 RMVar_ID_27234 Human_SNP_ID_720533250 A-to-I Human chrX + 71411107 71411107 71411107 ACCCGGCTGATTTTCTCTTTTGAAGCAGTCTCACTCTGTCACCCAGGCTGGAGGAGTGTGGTGGT ACCCGGCTGATTTTCTCTTTTGAAGCAGTCTCGCTCTGTCACCCAGGCTGGAGGAGTGTGGTGGT A G TAF1 Ensembl:ENSG00000147133 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956758127 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64295,RMVar_hsa_circ_355603,RMVar_hsa_circ_329396,RMVar_hsa_circ_302512,RMVar_hsa_circ_75437,RMVar_hsa_circ_104665,RMVar_hsa_circ_262929,RMVar_hsa_circ_262930,RMVar_hsa_circ_62329,RMVar_hsa_circ_374581,RMVar_hsa_circ_337595,RMVar_hsa_circ_295602,RMVar_hsa_circ_262935,RMVar_hsa_circ_29000,RMVar_hsa_circ_21188,RMVar_hsa_circ_90821,RMVar_hsa_circ_262938,RMVar_hsa_circ_67237,RMVar_hsa_circ_282933,RMVar_hsa_circ_32131,RMVar_hsa_circ_36045,RMVar_hsa_circ_5407,RMVar_hsa_circ_8206,RMVar_hsa_circ_14702 27235 RMVar_ID_27235 Human_SNP_ID_720534285 A-to-I Human chrX + 71417598 71417598 71417598 ATTGCCCAGGCTGGTCTCGAACTCCTGGGCTCAAGCGATCTGTCCACCTCAGCATCCCAAAGTGC ATTGCCCAGGCTGGTCTCGAACTCCTGGGCTCGAGCGATCTGTCCACCTCAGCATCCCAAAGTGC A G TAF1 Ensembl:ENSG00000147133 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1322626880 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_257440 RMVar_hsa_circ_64295,RMVar_hsa_circ_355603,RMVar_hsa_circ_329396,RMVar_hsa_circ_302512,RMVar_hsa_circ_75437,RMVar_hsa_circ_104665,RMVar_hsa_circ_262929,RMVar_hsa_circ_262930,RMVar_hsa_circ_62329,RMVar_hsa_circ_374581,RMVar_hsa_circ_337595,RMVar_hsa_circ_295602,RMVar_hsa_circ_262935,RMVar_hsa_circ_29000,RMVar_hsa_circ_21188,RMVar_hsa_circ_90821,RMVar_hsa_circ_262938,RMVar_hsa_circ_67237,RMVar_hsa_circ_282933,RMVar_hsa_circ_32131,RMVar_hsa_circ_36045,RMVar_hsa_circ_5407,RMVar_hsa_circ_8206,RMVar_hsa_circ_14702 27236 RMVar_ID_27236 Human_SNP_ID_720534834 A-to-I Human chrX + 71420259 71420259 71420259 ATCTGTTGTGCTGATTCCTGGTCTGTTGGTTCATTTTGGGATCACCTTGATTTGCCTTCCTCTAA ATCTGTTGTGCTGATTCCTGGTCTGTTGGTTCGTTTTGGGATCACCTTGATTTGCCTTCCTCTAA A G TAF1 Ensembl:ENSG00000147133 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879039537 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16921660 RMVar_hsa_circ_64295,RMVar_hsa_circ_355603,RMVar_hsa_circ_329396,RMVar_hsa_circ_302512,RMVar_hsa_circ_75437,RMVar_hsa_circ_104665,RMVar_hsa_circ_262929,RMVar_hsa_circ_262930,RMVar_hsa_circ_62329,RMVar_hsa_circ_374581,RMVar_hsa_circ_337595,RMVar_hsa_circ_295602,RMVar_hsa_circ_262935,RMVar_hsa_circ_29000,RMVar_hsa_circ_21188,RMVar_hsa_circ_90821,RMVar_hsa_circ_262938,RMVar_hsa_circ_67237,RMVar_hsa_circ_282933,RMVar_hsa_circ_32131,RMVar_hsa_circ_36045,RMVar_hsa_circ_5407,RMVar_hsa_circ_8206,RMVar_hsa_circ_14702 27237 RMVar_ID_27237 Human_SNP_ID_720534908 A-to-I Human chrX - 71420666 71420666 71420666 AGCCATGACTGGTCGAGGGTGACCCGGAAGACAGCGCCATTGAGGATCCGGAGCTGGAAGCTATC AGCCATGACTGGTCGAGGGTGACCCGGAAGACGGCGCCATTGAGGATCCGGAGCTGGAAGCTATC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878914997 Functional Loss SNV dbSNP153 33..33 33 - - - 27238 RMVar_ID_27238 Human_SNP_ID_720536271 A-to-I Human chrX + 71427752 71427752 71427752 CCTTAGGTCGGCAGTTTGAGATCAGCCTGGCCAAGATGGTGAAATCCCATCTTTCCTAAAAATAC CCTTAGGTCGGCAGTTTGAGATCAGCCTGGCCGAGATGGTGAAATCCCATCTTTCCTAAAAATAC A G TAF1 Ensembl:ENSG00000147133 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs950646642 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_329396,RMVar_hsa_circ_104665,RMVar_hsa_circ_262930,RMVar_hsa_circ_62329,RMVar_hsa_circ_374581,RMVar_hsa_circ_337595,RMVar_hsa_circ_262935,RMVar_hsa_circ_39147,RMVar_hsa_circ_37337,RMVar_hsa_circ_337587,RMVar_hsa_circ_73544,RMVar_hsa_circ_42500 27239 RMVar_ID_27239 Human_SNP_ID_720560921 A-to-I Human chrX + 71565694 71565694 71565694 CAAACTTTTTCTTAAAGGGCCAGATGGTAAATATTTTCAGTTTTGTGGTCCATGCTGTTTCACGT CAAACTTTTTCTTAAAGGGCCAGATGGTAAATGTTTTCAGTTTTGTGGTCCATGCTGTTTCACGT A G OGT Ensembl:ENSG00000147162 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1176638191 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2461,RMVar_hsa_circ_33519,RMVar_hsa_circ_74642,RMVar_hsa_circ_273976,RMVar_hsa_circ_368795,RMVar_hsa_circ_115894,RMVar_hsa_circ_262957,RMVar_hsa_circ_367763,RMVar_hsa_circ_262960,RMVar_hsa_circ_40580,RMVar_hsa_circ_121458,RMVar_hsa_circ_262961,RMVar_hsa_circ_100456,RMVar_hsa_circ_262965,RMVar_hsa_circ_375929,RMVar_hsa_circ_262967 27240 RMVar_ID_27240 Human_SNP_ID_720657908 A-to-I Human chrX + 72188363 72188363 72188363 TGCACTGCATATGGCTTTAGCTACTTTTTTTTATTTTTTTTTTTGAGACGGAGTTTCACTCTTGT TGCACTGCATATGGCTTTAGCTACTTTTTTTTGTTTTTTTTTTTGAGACGGAGTTTCACTCTTGT A G PIN4 Ensembl:ENSG00000102309 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs766592433 Functional Loss SNV dbSNP153 33..33 33 - - - 27241 RMVar_ID_27241 Human_SNP_ID_720657909 A-to-I Human chrX + 72188363 72188363 72188363 TGCACTGCATATGGCTTTAGCTACTTTTTTTTATTTTTTTTTTTGAGACGGAGTTTCACTCTTGT TGCACTGCATATGGCTTTAGCTACTTTTTTTTTTTTTTTTTTTTGAGACGGAGTTTCACTCTTGT A T PIN4 Ensembl:ENSG00000102309 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs766592433 Functional Loss SNV dbSNP153 33..33 33 - - - 27242 RMVar_ID_27242 Human_SNP_ID_720683487 A-to-I Human chrX - 72336841 72336841 72336841 GGAGGCTGAGGTGGGAGGATCACTTGAGCCCAAGAAGTCAAGACTGAAGTGAGCTGTGATCACAC GGAGGCTGAGGTGGGAGGATCACTTGAGCCCATGAAGTCAAGACTGAAGTGAGCTGTGATCACAC T A HDAC8,AL133500.1 Ensembl:ENSG00000147099,Ensembl:ENSG00000285547 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1365312377 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124992,RMVar_hsa_circ_262992,RMVar_hsa_circ_108842,RMVar_hsa_circ_262991 27243 RMVar_ID_27243 Human_SNP_ID_720685831 A-to-I Human chrX - 72351191 72351191 72351191 AGAGGCTGAGGCAGGAGGATCCCTTGAGCCCAAGAGGTTGAGGCTGCAGTGAGCCATGCCCACAC AGAGGCTGAGGCAGGAGGATCCCTTGAGCCCAGGAGGTTGAGGCTGCAGTGAGCCATGCCCACAC T C HDAC8,AL133500.1 Ensembl:ENSG00000147099,Ensembl:ENSG00000285547 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1421916739 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124992,RMVar_hsa_circ_262992,RMVar_hsa_circ_108842,RMVar_hsa_circ_262991 27244 RMVar_ID_27244 Human_SNP_ID_720717021 A-to-I Human chrX - 72552227 72552227 72552227 GAACTCCTGGCCTCAGGTGATCCTCCCACCTCAGCTTCCCAGAGTGCTAGGATTATAGGCGTGAG GAACTCCTGGCCTCAGGTGATCCTCCCACCTCGGCTTCCCAGAGTGCTAGGATTATAGGCGTGAG T C HDAC8,AL133500.1 Ensembl:ENSG00000147099,Ensembl:ENSG00000285547 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388829021 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78337,RMVar_hsa_circ_262992,RMVar_hsa_circ_108842,RMVar_hsa_circ_262999,RMVar_hsa_circ_61241,RMVar_hsa_circ_266524 27245 RMVar_ID_27245 Human_SNP_ID_720739254 A-to-I Human chrX - 72683187 72683187 72683187 GCAATTCACCCTCCTAGGCCTCTCAAAGTGCTAGGATTACAGGCATGAGCCACCACACCTGGCCT GCAATTCACCCTCCTAGGCCTCTCAAAGTGCTGGGATTACAGGCATGAGCCACCACACCTGGCCT T C PHKA1 Ensembl:ENSG00000067177 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1455969951 Functional Loss SNV dbSNP153 33..33 33 - - - 27246 RMVar_ID_27246 Human_SNP_ID_720816970 A-to-I Human chrX - 73223244 73223244 73223244 TCTCTCCTTGGCAAGCTTCTGTTTCTTTCTTCATTCTCGAAGCCTGTTCTTGAAGTTGGGGTCAC TCTCTCCTTGGCAAGCTTCTGTTTCTTTCTTCGTTCTCGAAGCCTGTTCTTGAAGTTGGGGTCAC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879047307 Functional Loss SNV dbSNP153 33..33 33 - - - 27247 RMVar_ID_27247 Human_SNP_ID_720975583 A-to-I Human chrX + 73947058 73947058 73947058 TGACTGCAACCTCCACCTCCTGGATTCAAGCTATTCTCCTGCCTCAGCCTGCCGAGTAGCTGGGA TGACTGCAACCTCCACCTCCTGGATTCAAGCTGTTCTCCTGCCTCAGCCTGCCGAGTAGCTGGGA A G JPX Ensembl:ENSG00000225470 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs11542569 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5107600,Human_RBP_ID_26291334 Human_Splice_Rec_2219259,Human_Splice_Rec_2219311,Human_Splice_Rec_2219342,Human_Splice_Rec_2219345,Human_Splice_Rec_2219373,Human_Splice_Rec_2219407,Human_Splice_Rec_2219423,Human_Splice_Rec_2219445,Human_Splice_Rec_2219480,Human_Splice_Rec_2219488,Human_Splice_Rec_2219512,Human_Splice_Rec_2219568,Human_Splice_Rec_2219678,Human_Splice_Rec_2219724,Human_Splice_Rec_2219811 RMVar_hsa_circ_82018,RMVar_hsa_circ_96572,RMVar_hsa_circ_99285,RMVar_hsa_circ_263030,RMVar_hsa_circ_263031,RMVar_hsa_circ_102420,RMVar_hsa_circ_263032,RMVar_hsa_circ_263033 27248 RMVar_ID_27248 Human_SNP_ID_720975586 A-to-I Human chrX + 73947071 73947071 73947071 CACCTCCTGGATTCAAGCTATTCTCCTGCCTCAGCCTGCCGAGTAGCTGGGATTACAGGCATGTG CACCTCCTGGATTCAAGCTATTCTCCTGCCTCGGCCTGCCGAGTAGCTGGGATTACAGGCATGTG A G JPX Ensembl:ENSG00000225470 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11542576 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5107600 Human_Splice_Rec_2219259,Human_Splice_Rec_2219311,Human_Splice_Rec_2219342,Human_Splice_Rec_2219345,Human_Splice_Rec_2219373,Human_Splice_Rec_2219407,Human_Splice_Rec_2219423,Human_Splice_Rec_2219445,Human_Splice_Rec_2219480,Human_Splice_Rec_2219488,Human_Splice_Rec_2219512,Human_Splice_Rec_2219568,Human_Splice_Rec_2219678,Human_Splice_Rec_2219724,Human_Splice_Rec_2219811 RMVar_hsa_circ_82018,RMVar_hsa_circ_96572,RMVar_hsa_circ_99285,RMVar_hsa_circ_263030,RMVar_hsa_circ_263031,RMVar_hsa_circ_102420,RMVar_hsa_circ_263032,RMVar_hsa_circ_263033 27249 RMVar_ID_27249 Human_SNP_ID_720975602 A-to-I Human chrX + 73947127 73947127 73947127 AGGCATGTGCCACCGCACCCAGCTAATTTTGTATTTTTTAGTAGAGATGGGGTTTCTCCATGTTG AGGCATGTGCCACCGCACCCAGCTAATTTTGTGTTTTTTAGTAGAGATGGGGTTTCTCCATGTTG A G JPX Ensembl:ENSG00000225470 lincRNA intron GSE100210;GSE99789 HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 29129909,29796672 RNA-Seq:(High) rs11542572 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8277973 RMVar_hsa_circ_82018,RMVar_hsa_circ_96572,RMVar_hsa_circ_99285,RMVar_hsa_circ_263030,RMVar_hsa_circ_263031,RMVar_hsa_circ_102420,RMVar_hsa_circ_263032,RMVar_hsa_circ_263033 27250 RMVar_ID_27250 Human_SNP_ID_720975604 A-to-I Human chrX + 73947137 73947137 73947137 CACCGCACCCAGCTAATTTTGTATTTTTTAGTAGAGATGGGGTTTCTCCATGTTGGTCAGGCTGG CACCGCACCCAGCTAATTTTGTATTTTTTAGTGGAGATGGGGTTTCTCCATGTTGGTCAGGCTGG A G JPX Ensembl:ENSG00000225470 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs11542570 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8033707,Human_RBP_ID_8277973 RMVar_hsa_circ_82018,RMVar_hsa_circ_96572,RMVar_hsa_circ_99285,RMVar_hsa_circ_263030,RMVar_hsa_circ_263031,RMVar_hsa_circ_102420,RMVar_hsa_circ_263032,RMVar_hsa_circ_263033 27251 RMVar_ID_27251 Human_SNP_ID_720976419 A-to-I Human chrX + 73951374 73951374 73951374 TGACCTCGTGATCCGCCCTCCTCGGCCTCGCAAAGTGCTGGGATTATAGTCGTTAGCCACCGCAC TGACCTCGTGATCCGCCCTCCTCGGCCTCGCAGAGTGCTGGGATTATAGTCGTTAGCCACCGCAC A G JPX Ensembl:ENSG00000225470 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978399867 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5252138 RMVar_hsa_circ_82018,RMVar_hsa_circ_99285,RMVar_hsa_circ_263031,RMVar_hsa_circ_263033 27252 RMVar_ID_27252 Human_SNP_ID_720976568 A-to-I Human chrX + 73952252 73952252 73952252 CAGCATGGCCAACATGGCAAAACCCCATTTCTACTAGAAATACAAAAAATTAGCCAGGCGTGGTG CAGCATGGCCAACATGGCAAAACCCCATTTCTGCTAGAAATACAAAAAATTAGCCAGGCGTGGTG A G JPX Ensembl:ENSG00000225470 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs767002518 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82018,RMVar_hsa_circ_99285,RMVar_hsa_circ_263031,RMVar_hsa_circ_263033 27253 RMVar_ID_27253 Human_SNP_ID_720976570 A-to-I Human chrX + 73952265 73952265 73952265 ATGGCAAAACCCCATTTCTACTAGAAATACAAAAAATTAGCCAGGCGTGGTGGCACACACCTGTA ATGGCAAAACCCCATTTCTACTAGAAATACAAGAAATTAGCCAGGCGTGGTGGCACACACCTGTA A G JPX Ensembl:ENSG00000225470 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1389633598 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82018,RMVar_hsa_circ_99285,RMVar_hsa_circ_263031,RMVar_hsa_circ_263033 27254 RMVar_ID_27254 Human_SNP_ID_720976574 A-to-I Human chrX + 73952287 73952285 73952287 AGAAATACAAAAAATTAGCCAGGCGTGGTGGCACACACCTGTAGTCCCAGATACTCGAGAGGCTG AGAAATACAAAAAATTAGCCAGGCGTGGTGG__CACACCTGTAGTCCCAGATACTCGAGAGGCTG GCA G JPX Ensembl:ENSG00000225470 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1425614301 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_8277978,Human_RBP_ID_26307689 RMVar_hsa_circ_82018,RMVar_hsa_circ_99285,RMVar_hsa_circ_263031,RMVar_hsa_circ_263033 27255 RMVar_ID_27255 Human_SNP_ID_720976960 A-to-I Human chrX + 73954106 73954106 73954106 CCTTAGCCTCCCAAAGTGCTGGGATTACAGGTATGAGCCACTGCGCCCGGAATGAATCACATTTC CCTTAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACTGCGCCCGGAATGAATCACATTTC A G JPX Ensembl:ENSG00000225470 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs766986103 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5252149,Human_RBP_ID_5272566,Human_RBP_ID_8277982,Human_RBP_ID_16932752,Human_RBP_ID_23204356 RMVar_hsa_circ_82018,RMVar_hsa_circ_99285,RMVar_hsa_circ_263031,RMVar_hsa_circ_263033 27256 RMVar_ID_27256 Human_SNP_ID_720977175 A-to-I Human chrX + 73955425 73955425 73955425 CTTTGGGAGGCAGAGGTGGGCTGATCACCTGGAGGTCAGGAGTTTGAGACCAGCCTGACCAACGT CTTTGGGAGGCAGAGGTGGGCTGATCACCTGGGGGTCAGGAGTTTGAGACCAGCCTGACCAACGT A G JPX Ensembl:ENSG00000225470 lincRNA intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1419674769 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10471148,Human_RBP_ID_23109600,Human_RBP_ID_26307705 RMVar_hsa_circ_82018,RMVar_hsa_circ_99285,RMVar_hsa_circ_263031,RMVar_hsa_circ_263033 27257 RMVar_ID_27257 Human_SNP_ID_720977177 A-to-I Human chrX + 73955430 73955430 73955430 GGAGGCAGAGGTGGGCTGATCACCTGGAGGTCAGGAGTTTGAGACCAGCCTGACCAACGTGAAGA GGAGGCAGAGGTGGGCTGATCACCTGGAGGTCGGGAGTTTGAGACCAGCCTGACCAACGTGAAGA A G JPX Ensembl:ENSG00000225470 lincRNA intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1022985877 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10471148,Human_RBP_ID_23109600,Human_RBP_ID_26307705 RMVar_hsa_circ_82018,RMVar_hsa_circ_99285,RMVar_hsa_circ_263031,RMVar_hsa_circ_263033 27258 RMVar_ID_27258 Human_SNP_ID_720977211 A-to-I Human chrX + 73955582 73955582 73955582 GGATCATGAGGTCAGGAGATCAAGACCATCCTAGCTAAGATGAGGAAACCCCGTCTTTACTAAAA GGATCATGAGGTCAGGAGATCAAGACCATCCTGGCTAAGATGAGGAAACCCCGTCTTTACTAAAA A G JPX Ensembl:ENSG00000225470 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350937232 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5252567 RMVar_hsa_circ_82018,RMVar_hsa_circ_99285,RMVar_hsa_circ_263031,RMVar_hsa_circ_263033 27259 RMVar_ID_27259 Human_SNP_ID_720977267 A-to-I Human chrX + 73955840 73955840 73955840 CCTGTAATCTCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCTTGAACCTGGGAAGCGGATGTT CCTGTAATCTCAGCTACTCGGGAGGCTGAGGCGGGAGAATTGCTTGAACCTGGGAAGCGGATGTT A G JPX Ensembl:ENSG00000225470 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs758658449 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26291585 RMVar_hsa_circ_82018,RMVar_hsa_circ_99285,RMVar_hsa_circ_263031,RMVar_hsa_circ_263033 27260 RMVar_ID_27260 Human_SNP_ID_720977386 A-to-I Human chrX + 73956488 73956482 73956488 GCTAATTTTTGTTTTAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCGCG GCTAATTTTTGTTTTAGTGATTCTCCT______GCCTCCCGAGTAGCTGGGACTACAGGCGCGCG TGCCTCA T JPX Ensembl:ENSG00000225470 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1443022978 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_16932833,Human_RBP_ID_26291596 RMVar_hsa_circ_82018,RMVar_hsa_circ_99285,RMVar_hsa_circ_263031,RMVar_hsa_circ_263033 27261 RMVar_ID_27261 Human_SNP_ID_720979873 A-to-I Human chrX + 73968871 73968871 73968871 GTAGCTGGGATTACAGGCATGCGCCACGACGCAAGAAAATCACTTGAACACAGGAGGTGGAAGTT GTAGCTGGGATTACAGGCATGCGCCACGACGCGAGAAAATCACTTGAACACAGGAGGTGGAAGTT A G JPX Ensembl:ENSG00000225470 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1282933809 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3932098,Human_RBP_ID_8277137,Human_RBP_ID_18522096 RMVar_hsa_circ_82018,RMVar_hsa_circ_99285,RMVar_hsa_circ_263031,RMVar_hsa_circ_263033 27262 RMVar_ID_27262 Human_SNP_ID_720982079 A-to-I Human chrX + 73980536 73980536 73980536 TCGCCCAGGCTGGAGTGCAGTGGCATGATCTCAGCTTACTGCAAGCTCCGCCTCTCGGGTTCACG TCGCCCAGGCTGGAGTGCAGTGGCATGATCTCGGCTTACTGCAAGCTCCGCCTCTCGGGTTCACG A G JPX Ensembl:ENSG00000225470 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1347845594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8032198 RMVar_hsa_circ_82018,RMVar_hsa_circ_99285,RMVar_hsa_circ_263031,RMVar_hsa_circ_263033 27263 RMVar_ID_27263 Human_SNP_ID_720984005 A-to-I Human chrX + 73990366 73990364 73990366 CTGGCCAACATGGCGAAACCCGGTCTCTACTAAAAATACAAAAGTTAGCTGAGTGTGGTGGTGGG CTGGCCAACATGGCGAAACCCGGTCTCTACT__AAATACAAAAGTTAGCTGAGTGTGGTGGTGGG TAA T JPX Ensembl:ENSG00000225470 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1266822251 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_8277141 RMVar_hsa_circ_82018,RMVar_hsa_circ_99285,RMVar_hsa_circ_263031,RMVar_hsa_circ_263033 27264 RMVar_ID_27264 Human_SNP_ID_720984007 A-to-I Human chrX + 73990371 73990371 73990371 CAACATGGCGAAACCCGGTCTCTACTAAAAATACAAAAGTTAGCTGAGTGTGGTGGTGGGCGCCT CAACATGGCGAAACCCGGTCTCTACTAAAAATGCAAAAGTTAGCTGAGTGTGGTGGTGGGCGCCT A G JPX Ensembl:ENSG00000225470 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1021548006 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8277141 RMVar_hsa_circ_82018,RMVar_hsa_circ_99285,RMVar_hsa_circ_263031,RMVar_hsa_circ_263033 27265 RMVar_ID_27265 Human_SNP_ID_720984115 A-to-I Human chrX + 73990949 73990949 73990949 TTACTGCAACCTCCGCTTCCTGGGTTCAAGCTATTCTGCATGCCTCAGCCTCCCGAGTAGCTGGT TTACTGCAACCTCCGCTTCCTGGGTTCAAGCTGTTCTGCATGCCTCAGCCTCCCGAGTAGCTGGT A G JPX Ensembl:ENSG00000225470 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1426910586 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8021700,Human_RBP_ID_10471815,Human_RBP_ID_24352490 RMVar_hsa_circ_82018,RMVar_hsa_circ_99285,RMVar_hsa_circ_263031,RMVar_hsa_circ_263033 27266 RMVar_ID_27266 Human_SNP_ID_720984264 A-to-I Human chrX + 73991944 73991944 73991944 GCTCACTGTAACCTCTGCCTACTGGTTCAAGCAGTTCTGGTGCCTGAGCCTCCCAAGTAGCTGGG GCTCACTGTAACCTCTGCCTACTGGTTCAAGCGGTTCTGGTGCCTGAGCCTCCCAAGTAGCTGGG A G JPX Ensembl:ENSG00000225470 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1398362611 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_739174,Human_RBP_ID_16934427,Human_RBP_ID_26308052 RMVar_hsa_circ_82018,RMVar_hsa_circ_99285,RMVar_hsa_circ_263031,RMVar_hsa_circ_263033 27267 RMVar_ID_27267 Human_SNP_ID_720984266 A-to-I Human chrX + 73991970 73991970 73991970 TCAAGCAGTTCTGGTGCCTGAGCCTCCCAAGTAGCTGGGATTACAGGCATGTGCCACCACTAGCC TCAAGCAGTTCTGGTGCCTGAGCCTCCCAAGTGGCTGGGATTACAGGCATGTGCCACCACTAGCC A G JPX Ensembl:ENSG00000225470 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913358451 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82018,RMVar_hsa_circ_99285,RMVar_hsa_circ_263031,RMVar_hsa_circ_263033 27268 RMVar_ID_27268 Human_SNP_ID_720984268 A-to-I Human chrX + 73991982 73991982 73991982 GGTGCCTGAGCCTCCCAAGTAGCTGGGATTACAGGCATGTGCCACCACTAGCCCCAGCTAATTTT GGTGCCTGAGCCTCCCAAGTAGCTGGGATTACGGGCATGTGCCACCACTAGCCCCAGCTAATTTT A G JPX Ensembl:ENSG00000225470 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946104945 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82018,RMVar_hsa_circ_99285,RMVar_hsa_circ_263031,RMVar_hsa_circ_263033 27269 RMVar_ID_27269 Human_SNP_ID_720984275 A-to-I Human chrX + 73992009 73992009 73992009 ATTACAGGCATGTGCCACCACTAGCCCCAGCTAATTTTTAAATTTTTAGTAGAGATGGATTTCTT ATTACAGGCATGTGCCACCACTAGCCCCAGCTGATTTTTAAATTTTTAGTAGAGATGGATTTCTT A G JPX Ensembl:ENSG00000225470 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1343608186 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10480299,Human_RBP_ID_23105756,Human_RBP_ID_26292936 RMVar_hsa_circ_82018,RMVar_hsa_circ_99285,RMVar_hsa_circ_263031,RMVar_hsa_circ_263033 27270 RMVar_ID_27270 Human_SNP_ID_720984276 A-to-I Human chrX + 73992024 73992022 73992025 CACCACTAGCCCCAGCTAATTTTTAAATTTTTAGTAGAGATGGATTTCTTCATGTTGGCCAGGCT CACCACTAGCCCCAGCTAATTTTTAAATTTT___TAGAGATGGATTTCTTCATGTTGGCCAGGCT TTAG T JPX Ensembl:ENSG00000225470 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1213813928 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_10480299,Human_RBP_ID_23105756,Human_RBP_ID_26292936 RMVar_hsa_circ_82018,RMVar_hsa_circ_99285,RMVar_hsa_circ_263031,RMVar_hsa_circ_263033 27271 RMVar_ID_27271 Human_SNP_ID_720984277 A-to-I Human chrX + 73992027 73992027 73992027 CACTAGCCCCAGCTAATTTTTAAATTTTTAGTAGAGATGGATTTCTTCATGTTGGCCAGGCTGGT CACTAGCCCCAGCTAATTTTTAAATTTTTAGTTGAGATGGATTTCTTCATGTTGGCCAGGCTGGT A T JPX Ensembl:ENSG00000225470 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202594828 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82018,RMVar_hsa_circ_99285,RMVar_hsa_circ_263031,RMVar_hsa_circ_263033 27272 RMVar_ID_27272 Human_SNP_ID_720985115 A-to-I Human chrX + 73997067 73997067 73997067 TTTTAGTAGAAAAGGGGTTTCACCTTTTGGCCAGGCTGATCTCGAACTTCTGACCTCAAGCAATC TTTTAGTAGAAAAGGGGTTTCACCTTTTGGCCGGGCTGATCTCGAACTTCTGACCTCAAGCAATC A G JPX Ensembl:ENSG00000225470 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1161333325 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8034465,Human_RBP_ID_16934614,Human_RBP_ID_18924649 Human_Splice_Rec_2219494,Human_Splice_Rec_2219495,Human_Splice_Rec_2219582,Human_Splice_Rec_2219583,Human_Splice_Rec_2219616,Human_Splice_Rec_2219617,Human_Splice_Rec_2219626,Human_Splice_Rec_2219627 RMVar_hsa_circ_82018,RMVar_hsa_circ_263033,RMVar_hsa_circ_85062,RMVar_hsa_circ_263034 27273 RMVar_ID_27273 Human_SNP_ID_720985555 A-to-I Human chrX + 73999082 73999082 73999082 AAGCATGCACCACCACGCCCGTCTAATTTTGTATTTTCACTAGAGACGGGGTTTCTCCATGTTGG AAGCATGCACCACCACGCCCGTCTAATTTTGTGTTTTCACTAGAGACGGGGTTTCTCCATGTTGG A G JPX Ensembl:ENSG00000225470 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1569213533 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5073168,Human_RBP_ID_16934689 RMVar_hsa_circ_65518,RMVar_hsa_circ_82018,RMVar_hsa_circ_263033,RMVar_hsa_circ_85062,RMVar_hsa_circ_263034 27274 RMVar_ID_27274 Human_SNP_ID_720985824 A-to-I Human chrX + 74000608 74000608 74000608 GGGAGGCCGAGGCAGGCACATCACCTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGCAC GGGAGGCCGAGGCAGGCACATCACCTGAGGTCGGGAGTTCGAGACCAGCCTGGCCAACATGGCAC A G JPX Ensembl:ENSG00000225470 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956098749 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10480345,Human_RBP_ID_23105853,Human_RBP_ID_26308094 RMVar_hsa_circ_85062,RMVar_hsa_circ_263034 27275 RMVar_ID_27275 Human_SNP_ID_720987530 A-to-I Human chrX + 74008929 74008929 74008929 GTAATCCCAGCTACTCGGGAGTCTGAGGCAGTAGAATCACTTGAACCCAGGAGGTGGAGGTTGCA GTAATCCCAGCTACTCGGGAGTCTGAGGCAGTGGAATCACTTGAACCCAGGAGGTGGAGGTTGCA A G JPX Ensembl:ENSG00000225470 lincRNA exon GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1253651489 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85062,RMVar_hsa_circ_263034 27276 RMVar_ID_27276 Human_SNP_ID_720987532 A-to-I Human chrX + 74008935 74008935 74008935 CCAGCTACTCGGGAGTCTGAGGCAGTAGAATCACTTGAACCCAGGAGGTGGAGGTTGCAGTGAGC CCAGCTACTCGGGAGTCTGAGGCAGTAGAATCGCTTGAACCCAGGAGGTGGAGGTTGCAGTGAGC A G JPX Ensembl:ENSG00000225470 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs960625505 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85062,RMVar_hsa_circ_263034 27277 RMVar_ID_27277 Human_SNP_ID_720987534 A-to-I Human chrX + 74008945 74008945 74008945 GGGAGTCTGAGGCAGTAGAATCACTTGAACCCAGGAGGTGGAGGTTGCAGTGAGCGGAGATTGTG GGGAGTCTGAGGCAGTAGAATCACTTGAACCCGGGAGGTGGAGGTTGCAGTGAGCGGAGATTGTG A G JPX Ensembl:ENSG00000225470 lincRNA exon GSE107867 ASD brains,frontal_cortex;ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs993335763 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26293278 RMVar_hsa_circ_85062,RMVar_hsa_circ_263034 27278 RMVar_ID_27278 Human_SNP_ID_720987892 A-to-I Human chrX + 74010574 74010574 74010574 GTCAGGCTGGTCTCGAATTCCCGACCTCAGGTAATCTGCTCGCCTCTGCCTCCCAAAGTACTGGG GTCAGGCTGGTCTCGAATTCCCGACCTCAGGTGATCTGCTCGCCTCTGCCTCCCAAAGTACTGGG A G JPX Ensembl:ENSG00000225470 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1195287921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16934948,Human_RBP_ID_23204565,Human_RBP_ID_26293299,Human_RBP_ID_27553477 Human_Splice_Rec_2219247 RMVar_hsa_circ_85062,RMVar_hsa_circ_263034 27279 RMVar_ID_27279 Human_SNP_ID_721022644 A-to-I Human chrX - 74197083 74197083 74197083 TATATATTGGTGCAGCCATTATGGAAGACAGTATGGAGGTTCCTAAGTAAATTAAAAATAGAACT TATATATTGGTGCAGCCATTATGGAAGACAGTTTGGAGGTTCCTAAGTAAATTAAAAATAGAACT T A FTX Ensembl:ENSG00000230590 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1427898643 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3264386,Human_RBP_ID_9248899,Human_RBP_ID_10472168,Human_RBP_ID_23105974 27280 RMVar_ID_27280 Human_SNP_ID_721022646 A-to-I Human chrX - 74197090 74197090 74197090 AATGTATTATATATTGGTGCAGCCATTATGGAAGACAGTATGGAGGTTCCTAAGTAAATTAAAAA AATGTATTATATATTGGTGCAGCCATTATGGAGGACAGTATGGAGGTTCCTAAGTAAATTAAAAA T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs1477910383 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9248900 27281 RMVar_ID_27281 Human_SNP_ID_721022654 A-to-I Human chrX - 74197128 74197128 74197128 GTGTGGAGAAGAGGGAGCACTTGTACACTGTTAGTGGGAATGTATTATATATTGGTGCAGCCATT GTGTGGAGAAGAGGGAGCACTTGTACACTGTTGGTGGGAATGTATTATATATTGGTGCAGCCATT T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1199869759 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5272604,Human_RBP_ID_18407382,Human_RBP_ID_24352677 27282 RMVar_ID_27282 Human_SNP_ID_721022656 A-to-I Human chrX - 74197134 74197134 74197134 GTGAGGGTGTGGAGAAGAGGGAGCACTTGTACACTGTTAGTGGGAATGTATTATATATTGGTGCA GTGAGGGTGTGGAGAAGAGGGAGCACTTGTACGCTGTTAGTGGGAATGTATTATATATTGGTGCA T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1360741459 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3931437,Human_RBP_ID_18407382,Human_RBP_ID_24352677 27283 RMVar_ID_27283 Human_SNP_ID_721022659 A-to-I Human chrX - 74197151 74197151 74197151 AGAGCTAACAAGTGTTGGTGAGGGTGTGGAGAAGAGGGAGCACTTGTACACTGTTAGTGGGAATG AGAGCTAACAAGTGTTGGTGAGGGTGTGGAGAGGAGGGAGCACTTGTACACTGTTAGTGGGAATG T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1275706497 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8022226,Human_RBP_ID_16935464 27284 RMVar_ID_27284 Human_SNP_ID_721022664 A-to-I Human chrX - 74197174 74197172 74197174 GGATAGCTATTATCAAAAAGACAAGAGCTAACAAGTGTTGGTGAGGGTGTGGAGAAGAGGGAGCA GGATAGCTATTATCAAAAAGACAAGAGCTAAC__GTGTTGGTGAGGGTGTGGAGAAGAGGGAGCA CTT C FTX Ensembl:ENSG00000230590 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1400486074 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_8022226 27285 RMVar_ID_27285 Human_SNP_ID_721022665 A-to-I Human chrX - 74197174 74197174 74197174 GGATAGCTATTATCAAAAAGACAAGAGCTAACAAGTGTTGGTGAGGGTGTGGAGAAGAGGGAGCA GGATAGCTATTATCAAAAAGACAAGAGCTAACGAGTGTTGGTGAGGGTGTGGAGAAGAGGGAGCA T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1173322471 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8022226 27286 RMVar_ID_27286 Human_SNP_ID_721022671 A-to-I Human chrX - 74197202 74197202 74197202 ACTTTGAGATACCACCTCATACATGTTAGGATAGCTATTATCAAAAAGACAAGAGCTAACAAGTG ACTTTGAGATACCACCTCATACATGTTAGGATGGCTATTATCAAAAAGACAAGAGCTAACAAGTG T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,31158229,31158229,32596459 RNA-Seq:(High) rs1238183274 Functional Loss SNV dbSNP153 33..33 33 - - - 27287 RMVar_ID_27287 Human_SNP_ID_721022673 A-to-I Human chrX - 74197214 74197214 74197214 CAAATCAAAACTACTTTGAGATACCACCTCATACATGTTAGGATAGCTATTATCAAAAAGACAAG CAAATCAAAACTACTTTGAGATACCACCTCATGCATGTTAGGATAGCTATTATCAAAAAGACAAG T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1440670881 Functional Loss SNV dbSNP153 33..33 33 - - - 27288 RMVar_ID_27288 Human_SNP_ID_721022674 A-to-I Human chrX - 74197224 74197224 74197224 CAGGAAAATGCAAATCAAAACTACTTTGAGATACCACCTCATACATGTTAGGATAGCTATTATCA CAGGAAAATGCAAATCAAAACTACTTTGAGATGCCACCTCATACATGTTAGGATAGCTATTATCA T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1286608267 Functional Loss SNV dbSNP153 33..33 33 - - - 27289 RMVar_ID_27289 Human_SNP_ID_721022677 A-to-I Human chrX - 74197239 74197239 74197239 AATATCACCAGTCATCAGGAAAATGCAAATCAAAACTACTTTGAGATACCACCTCATACATGTTA AATATCACCAGTCATCAGGAAAATGCAAATCAGAACTACTTTGAGATACCACCTCATACATGTTA T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1255767857 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3273302 27290 RMVar_ID_27290 Human_SNP_ID_721022688 A-to-I Human chrX - 74197270 74197270 74197270 AAATGACCAACAGGTATATGAAATGGTGCTCAATATCACCAGTCATCAGGAAAATGCAAATCAAA AAATGACCAACAGGTATATGAAATGGTGCTCAGTATCACCAGTCATCAGGAAAATGCAAATCAAA T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1399745508 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3264388,Human_RBP_ID_17580072 27291 RMVar_ID_27291 Human_SNP_ID_721022694 A-to-I Human chrX - 74197312 74197312 74197312 TGGGGAAAGGACTTGAATAGACATTTCTTCAAAGATGACAGAAAATGACCAACAGGTATATGAAA TGGGGAAAGGACTTGAATAGACATTTCTTCAAGGATGACAGAAAATGACCAACAGGTATATGAAA T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1168778379 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3264390,Human_RBP_ID_17580073 27292 RMVar_ID_27292 Human_SNP_ID_721022720 A-to-I Human chrX - 74197444 74197444 74197444 ATGAAAAGGCAATGTACAGATAAGGAGAAAATATTTGCAAACCATATATCAGGCAAGGTTTTAAT ATGAAAAGGCAATGTACAGATAAGGAGAAAATGTTTGCAAACCATATATCAGGCAAGGTTTTAAT T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1329780973 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3264395,Human_RBP_ID_3931783,Human_RBP_ID_5108202,Human_RBP_ID_8277803 27293 RMVar_ID_27293 Human_SNP_ID_721023083 A-to-I Human chrX - 74199982 74199982 74199982 GATTTTGGCTATTCTTTCAGGTGCATAGTGGCATCTTATTGTTGTTTTAATTTGCAATTCCCTGA GATTTTGGCTATTCTTTCAGGTGCATAGTGGCGTCTTATTGTTGTTTTAATTTGCAATTCCCTGA T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1000360090 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3264461,Human_RBP_ID_3931786,Human_RBP_ID_8278329,Human_RBP_ID_10472198,Human_RBP_ID_26293447 27294 RMVar_ID_27294 Human_SNP_ID_721023302 A-to-I Human chrX - 74201300 74201300 74201300 TCTGATGGTATGGTCCTGACACCCTTGTAGAAATTCAATTGAAGATATATGTATGAGTTTACTTC TCTGATGGTATGGTCCTGACACCCTTGTAGAAGTTCAATTGAAGATATATGTATGAGTTTACTTC T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1004784902 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1718802,Human_RBP_ID_2078184,Human_RBP_ID_3264493,Human_RBP_ID_16935593,Human_RBP_ID_17580074,Human_RBP_ID_18924755,Human_RBP_ID_26308129 Human_miRNA_ID_3201487 27295 RMVar_ID_27295 Human_SNP_ID_721023415 A-to-I Human chrX - 74201942 74201942 74201942 CAACTTTTTGAAGAACTTCCCAACTGTTCTCCATGGTGGCTGTGCCATTGTATATTCCTACCAGC CAACTTTTTGAAGAACTTCCCAACTGTTCTCCTTGGTGGCTGTGCCATTGTATATTCCTACCAGC T A FTX Ensembl:ENSG00000230590 lincRNA intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs776019823 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3273316,Human_RBP_ID_8022266,Human_RBP_ID_9248923,Human_RBP_ID_16935610,Human_RBP_ID_17580077 27296 RMVar_ID_27296 Human_SNP_ID_721023416 A-to-I Human chrX - 74201942 74201942 74201942 CAACTTTTTGAAGAACTTCCCAACTGTTCTCCATGGTGGCTGTGCCATTGTATATTCCTACCAGC CAACTTTTTGAAGAACTTCCCAACTGTTCTCCGTGGTGGCTGTGCCATTGTATATTCCTACCAGC T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs776019823 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3273316,Human_RBP_ID_8022266,Human_RBP_ID_9248923,Human_RBP_ID_16935610,Human_RBP_ID_17580077 27297 RMVar_ID_27297 Human_SNP_ID_721023439 A-to-I Human chrX - 74202087 74202087 74202087 TGATTGGTTGTTTCTACTTTTTTTTAGCTATTATGAATAATATTGCTGTGAACATTTGTGTACAA TGATTGGTTGTTTCTACTTTTTTTTAGCTATTTTGAATAATATTGCTGTGAACATTTGTGTACAA T A FTX Ensembl:ENSG00000230590 lincRNA intron GSE100210;GSE107867;GSE107867 HepG2 cell line;ASD brains,cerebellum;ASD brains,frontal_cortex - 29129909,30559470,30559470 RNA-Seq:(High) rs1409703352 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3264511,Human_RBP_ID_3928279,Human_RBP_ID_8039408,Human_RBP_ID_10472221,Human_RBP_ID_18407394,Human_RBP_ID_26745952 Human_miRNA_ID_3183944,Human_miRNA_ID_3189698,Human_miRNA_ID_3208152 27298 RMVar_ID_27298 Human_SNP_ID_721024562 A-to-I Human chrX - 74208530 74208524 74208530 CAGGGTTTTGCCATGTTGCCCAAGCTGGTCTCAAACTCCTGGGCTCAAGAGATCCACCCACCTAG CAGGGTTTTGCCATGTTGCCCAAGCTGGTCTC______CTGGGCTCAAGAGATCCACCCACCTAG GGAGTTT G FTX Ensembl:ENSG00000230590 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1458134314 Functional Loss DEL dbSNP153 33..38 33 - - - 27299 RMVar_ID_27299 Human_SNP_ID_721024636 A-to-I Human chrX - 74208928 74208928 74208928 CCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGGATCCCTTGAACTCGGTGGCAGAGGTAC CCTGTAATCCCAGCTACTTGGGAGGCTGAGGCTGGAGGATCCCTTGAACTCGGTGGCAGAGGTAC T A FTX Ensembl:ENSG00000230590 lincRNA intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1028263058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8022327,Human_RBP_ID_16935865 27300 RMVar_ID_27300 Human_SNP_ID_721025425 A-to-I Human chrX - 74214377 74214377 74214377 GGGACTATAAGCACATGGCACCACACCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCA GGGACTATAAGCACATGGCACCACACCCAGCTTATTTTTGTATTTTTAGTAGAGATGGGGTTTCA T A FTX Ensembl:ENSG00000230590 lincRNA intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1189391976 Functional Loss SNV dbSNP153 33..33 33 - - - 27301 RMVar_ID_27301 Human_SNP_ID_721025460 A-to-I Human chrX - 74214531 74214531 74214531 TGTTTCAAATACATTCCTTCTTTGTGGCGGGGAGATGGAGTCTTGCTCTGTCGCCCAAGCTGGAG TGTTTCAAATACATTCCTTCTTTGTGGCGGGGGGATGGAGTCTTGCTCTGTCGCCCAAGCTGGAG T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs921676336 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16936109 27302 RMVar_ID_27302 Human_SNP_ID_721025840 A-to-I Human chrX - 74216853 74216853 74216853 AGGAGGCTGAGGCAGGAGAATCACTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCCGAGATCCCA AGGAGGCTGAGGCAGGAGAATCACTTGAACCCGGGAGGCGGAGGTTGCAGTGAGCCGAGATCCCA T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs899530956 Functional Loss SNV dbSNP153 33..33 33 - - - 27303 RMVar_ID_27303 Human_SNP_ID_721025841 A-to-I Human chrX - 74216853 74216853 74216853 AGGAGGCTGAGGCAGGAGAATCACTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCCGAGATCCCA AGGAGGCTGAGGCAGGAGAATCACTTGAACCCCGGAGGCGGAGGTTGCAGTGAGCCGAGATCCCA T G FTX Ensembl:ENSG00000230590 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs899530956 Functional Loss SNV dbSNP153 33..33 33 - - - 27304 RMVar_ID_27304 Human_SNP_ID_721026702 A-to-I Human chrX - 74222547 74222547 74222547 TTCCTTCCTTTCTGCATCTGGCTGTGTTGGCCAGGTTGGTCTTGAACTCCTGGGCTCAAGCAGTC TTCCTTCCTTTCTGCATCTGGCTGTGTTGGCCCGGTTGGTCTTGAACTCCTGGGCTCAAGCAGTC T G FTX Ensembl:ENSG00000230590 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1450316493 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1120967,Human_RBP_ID_21862797,Human_RBP_ID_26301483 27305 RMVar_ID_27305 Human_SNP_ID_721027058 A-to-I Human chrX - 74223788 74223788 74223788 CAGCCTGGCTAACATGGTGAAACACTGTCTCTACGAAAAGTACAAAAATTAGCCAGTCGGGGTGG CAGCCTGGCTAACATGGTGAAACACTGTCTCTCCGAAAAGTACAAAAATTAGCCAGTCGGGGTGG T G FTX Ensembl:ENSG00000230590 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs929326392 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16936616,Human_RBP_ID_26293889 27306 RMVar_ID_27306 Human_SNP_ID_721027261 A-to-I Human chrX - 74225019 74225019 74225019 CCAGGCTGGTCTTGAACTCTTGGGCTCAAGTAATCTGCTCACCTCAGCCTGCCAGTTTATCCTTT CCAGGCTGGTCTTGAACTCTTGGGCTCAAGTATTCTGCTCACCTCAGCCTGCCAGTTTATCCTTT T A FTX Ensembl:ENSG00000230590 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs368176618 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5252521,Human_RBP_ID_17580079,Human_RBP_ID_18924824,Human_RBP_ID_26308252 27307 RMVar_ID_27307 Human_SNP_ID_721027283 A-to-I Human chrX - 74225136 74225136 74225136 TCAAGCAATCCTCCCACATCAGCCTTCCGAGTAGCTGGGACTATAGGTGTATGCCACCACGCCCA TCAAGCAATCCTCCCACATCAGCCTTCCGAGTGGCTGGGACTATAGGTGTATGCCACCACGCCCA T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1026512355 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9249131,Human_RBP_ID_26293951 27308 RMVar_ID_27308 Human_SNP_ID_721027294 A-to-I Human chrX - 74225191 74225191 74225191 CAGGCTGGAGTGCAGTGGCACAATCGCAGCTCACTGCGTCCTCCACCTCCCAGGCTCAAGCAATC CAGGCTGGAGTGCAGTGGCACAATCGCAGCTCTCTGCGTCCTCCACCTCCCAGGCTCAAGCAATC T A FTX Ensembl:ENSG00000230590 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1453321592 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16936696,Human_RBP_ID_26293956 27309 RMVar_ID_27309 Human_SNP_ID_721027296 A-to-I Human chrX - 74225196 74225196 74225196 TTGCCCAGGCTGGAGTGCAGTGGCACAATCGCAGCTCACTGCGTCCTCCACCTCCCAGGCTCAAG TTGCCCAGGCTGGAGTGCAGTGGCACAATCGCTGCTCACTGCGTCCTCCACCTCCCAGGCTCAAG T A FTX Ensembl:ENSG00000230590 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264877742 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16936696,Human_RBP_ID_26293956 27310 RMVar_ID_27310 Human_SNP_ID_721027358 A-to-I Human chrX - 74225527 74225526 74225528 CCCGGGAGATGATGGCTGTGGTGAGCCGAGATAGCGCCGCTGCACTCCAGCCTGGGCGGCTGAGT CCCGGGAGATGATGGCTGTGGTGAGCCGAGA__GCGCCGCTGCACTCCAGCCTGGGCGGCTGAGT CTA C FTX Ensembl:ENSG00000230590 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1244016141 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_16936720,Human_RBP_ID_18154533,Human_RBP_ID_26308260 27311 RMVar_ID_27311 Human_SNP_ID_721030162 A-to-I Human chrX - 74243566 74243566 74243566 TGAGGTTGAGAGTTCGAGACCAGCCTGGGCCAACATGGTGAAACCCCGTCTCTACTTAAAAAAAA TGAGGTTGAGAGTTCGAGACCAGCCTGGGCCATCATGGTGAAACCCCGTCTCTACTTAAAAAAAA T A FTX Ensembl:ENSG00000230590 lincRNA intron GSE100210;GSE107867 HepG2 cell line;ASD brains,frontal_cortex - 29129909,30559470 RNA-Seq:(High) rs1488064929 Functional Loss SNV dbSNP153 33..33 33 - - - 27312 RMVar_ID_27312 Human_SNP_ID_721030246 A-to-I Human chrX - 74243987 74243987 74243987 CAGGCTGGAGTGCAGTGTCGTGATCTTGGCTCACTGCGGCCTCTGTCTCCTGGGTTCAAGCAATT CAGGCTGGAGTGCAGTGTCGTGATCTTGGCTCGCTGCGGCCTCTGTCTCCTGGGTTCAAGCAATT T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277827191 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5252526,Human_RBP_ID_16937827,Human_RBP_ID_18924861,Human_RBP_ID_26797336 27313 RMVar_ID_27313 Human_SNP_ID_721030254 A-to-I Human chrX - 74244006 74244006 74244006 AGGGTTTCGCTCTGTCACCCAGGCTGGAGTGCAGTGTCGTGATCTTGGCTCACTGCGGCCTCTGT AGGGTTTCGCTCTGTCACCCAGGCTGGAGTGCGGTGTCGTGATCTTGGCTCACTGCGGCCTCTGT T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1238097889 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24353012,Human_RBP_ID_26797336 27314 RMVar_ID_27314 Human_SNP_ID_721033072 A-to-I Human chrX - 74260716 74260716 74260716 ATCACAGGCCGATCTCAAACTAGGCTGGTCTCAAACTCCTGGGCTAAAACAGATCACCCGCCTGA ATCACAGGCCGATCTCAAACTAGGCTGGTCTCCAACTCCTGGGCTAAAACAGATCACCCGCCTGA T G FTX Ensembl:ENSG00000230590 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1018136783 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3931855,Human_RBP_ID_8031394,Human_RBP_ID_8278075,Human_RBP_ID_16938801,Human_RBP_ID_22843293 27315 RMVar_ID_27315 Human_SNP_ID_721033101 A-to-I Human chrX - 74260871 74260871 74260871 TGCAGTGGCATGATCATGGCTCACTATCCTCAACTTTTCAGTCTCAAGTAATTCTCCCACCTCAG TGCAGTGGCATGATCATGGCTCACTATCCTCAGCTTTTCAGTCTCAAGTAATTCTCCCACCTCAG T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1484455496 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3265819,Human_RBP_ID_8032767,Human_RBP_ID_16938818,Human_RBP_ID_17060758,Human_RBP_ID_18154583,Human_RBP_ID_24353145 27316 RMVar_ID_27316 Human_SNP_ID_721033103 A-to-I Human chrX - 74260888 74260888 74260888 TATCACTCAGGCTGGAGTGCAGTGGCATGATCATGGCTCACTATCCTCAACTTTTCAGTCTCAAG TATCACTCAGGCTGGAGTGCAGTGGCATGATCTTGGCTCACTATCCTCAACTTTTCAGTCTCAAG T A FTX Ensembl:ENSG00000230590 lincRNA intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs939643743 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16938823,Human_RBP_ID_18154583,Human_RBP_ID_23317714 27317 RMVar_ID_27317 Human_SNP_ID_721033218 A-to-I Human chrX - 74261720 74261720 74261720 GCTGGAGTGCAGTGGCAAGATCTCGGCTCATTACAAACCCTGCCTCTCAGGTTCAAGCTATTCTC GCTGGAGTGCAGTGGCAAGATCTCGGCTCATTGCAAACCCTGCCTCTCAGGTTCAAGCTATTCTC T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1213987011 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10473208,Human_RBP_ID_26294920 27318 RMVar_ID_27318 Human_SNP_ID_721033224 A-to-I Human chrX - 74261766 74261761 74261767 TTATTACTTTTATTTTTTTGAGACAGAGTCTCAGTCTGTCACCCAGGCTGGAGTGCAGTGGCAAG TTATTACTTTTATTTTTTTGAGACAGAGTCT______GTCACCCAGGCTGGAGTGCAGTGGCAAG CAGACTG C FTX Ensembl:ENSG00000230590 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs747947294 Functional Loss DEL dbSNP153 32..37 33 - - - Human_RBP_ID_8023335,Human_RBP_ID_16938879 27319 RMVar_ID_27319 Human_SNP_ID_721033667 A-to-I Human chrX - 74264449 74264449 74264449 TTTGTATTTTTGTATAGATGGGAGGTTTCACCATGTTGGCCAGGCTGGTCAAGTGATCCGCCTGC TTTGTATTTTTGTATAGATGGGAGGTTTCACCGTGTTGGCCAGGCTGGTCAAGTGATCCGCCTGC T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1199535373 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16939059,Human_RBP_ID_17580084 27320 RMVar_ID_27320 Human_SNP_ID_721033852 A-to-I Human chrX - 74265537 74265537 74265537 CTAGCTGCATGCAGCTGGAATGGAGTGGCACAATCTTGGCTCACTGCAACCTCTGCCTCCCGGGT CTAGCTGCATGCAGCTGGAATGGAGTGGCACAGTCTTGGCTCACTGCAACCTCTGCCTCCCGGGT T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1370319854 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8023403,Human_RBP_ID_16939116 27321 RMVar_ID_27321 Human_SNP_ID_721033976 A-to-I Human chrX - 74266004 74266004 74266004 GTACCTGTAGTCCCAGGCTGACGTAGGAGGATAGCTCGAGCCTGGGAGGTGGAGGTTGCAGTGAA GTACCTGTAGTCCCAGGCTGACGTAGGAGGATGGCTCGAGCCTGGGAGGTGGAGGTTGCAGTGAA T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE100210;GSE107867 HepG2 cell line;ASD brains,frontal_cortex - 29129909,30559470 RNA-Seq:(High) rs1441296040 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3931490,Human_RBP_ID_8023411,Human_RBP_ID_16939146,Human_RBP_ID_17580085 27322 RMVar_ID_27322 Human_SNP_ID_721033993 A-to-I Human chrX - 74266093 74266093 74266093 GCCCAAGAGTTTGAGACCAGCCTGGGCAACATAGTAAGACCCTGCCTGTACTAAAAATTTTAAAA GCCCAAGAGTTTGAGACCAGCCTGGGCAACATGGTAAGACCCTGCCTGTACTAAAAATTTTAAAA T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1276870841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23204658 27323 RMVar_ID_27323 Human_SNP_ID_721034005 A-to-I Human chrX - 74266120 74266120 74266120 GGAGGTCAAGGTGGGTGGATCACTTGAGCCCAAGAGTTTGAGACCAGCCTGGGCAACATAGTAAG GGAGGTCAAGGTGGGTGGATCACTTGAGCCCAGGAGTTTGAGACCAGCCTGGGCAACATAGTAAG T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1426828217 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16939153,Human_RBP_ID_17580087,Human_RBP_ID_26295026 27324 RMVar_ID_27324 Human_SNP_ID_721034016 A-to-I Human chrX - 74266153 74266153 74266153 GCGGTGGTTCCTACCTATAATCCCAGCACTTCAGGAGGTCAAGGTGGGTGGATCACTTGAGCCCA GCGGTGGTTCCTACCTATAATCCCAGCACTTCGGGAGGTCAAGGTGGGTGGATCACTTGAGCCCA T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1427989839 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16939155,Human_RBP_ID_17580087 27325 RMVar_ID_27325 Human_SNP_ID_721034067 A-to-I Human chrX - 74266285 74266285 74266285 AGGCGGGAGGATCGTTTGAGCTCAGCAGTTCAAGACCAGCCTGGGCATCATAGTGAGACCCTGTC AGGCGGGAGGATCGTTTGAGCTCAGCAGTTCACGACCAGCCTGGGCATCATAGTGAGACCCTGTC T G FTX Ensembl:ENSG00000230590 lincRNA intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs927481136 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16939157,Human_RBP_ID_23204659,Human_RBP_ID_26295037 27326 RMVar_ID_27326 Human_SNP_ID_721034519 A-to-I Human chrX - 74268896 74268896 74268896 TTCTCCTGCCTCAACCTCGAATACCTGGGATTACAGGCACCAGCCACCATGCCTGGCTAATTTTT TTCTCCTGCCTCAACCTCGAATACCTGGGATTGCAGGCACCAGCCACCATGCCTGGCTAATTTTT T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1219892652 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16939323 27327 RMVar_ID_27327 Human_SNP_ID_721035447 A-to-I Human chrX - 74274796 74274796 74274796 CCATTCAGAGTTATTTGATTCACAGTGTGTATAATATAATAAAAATAATACAGCTGTATTTGAGT CCATTCAGAGTTATTTGATTCACAGTGTGTATTATATAATAAAAATAATACAGCTGTATTTGAGT T A FTX Ensembl:ENSG00000230590 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs174162 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1719079,Human_RBP_ID_2078583,Human_RBP_ID_3266069,Human_RBP_ID_3928627,Human_RBP_ID_9249535,Human_RBP_ID_10473468,Human_RBP_ID_21997846,Human_RBP_ID_26295331 GWAS_ID_2779,GWAS_ID_2780,GWAS_ID_2781,GWAS_ID_2782,GWAS_ID_2783,GWAS_ID_2784 RMVar_hsa_circ_335579,RMVar_hsa_circ_342788 27328 RMVar_ID_27328 Human_SNP_ID_721035448 A-to-I Human chrX - 74274796 74274796 74274796 CCATTCAGAGTTATTTGATTCACAGTGTGTATAATATAATAAAAATAATACAGCTGTATTTGAGT CCATTCAGAGTTATTTGATTCACAGTGTGTATGATATAATAAAAATAATACAGCTGTATTTGAGT T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs174162 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1719079,Human_RBP_ID_2078583,Human_RBP_ID_3266069,Human_RBP_ID_3928627,Human_RBP_ID_9249535,Human_RBP_ID_10473468,Human_RBP_ID_21997846,Human_RBP_ID_26295331 GWAS_ID_2779,GWAS_ID_2780,GWAS_ID_2781,GWAS_ID_2782,GWAS_ID_2783,GWAS_ID_2784 RMVar_hsa_circ_335579,RMVar_hsa_circ_342788 27329 RMVar_ID_27329 Human_SNP_ID_721035491 A-to-I Human chrX - 74275058 74275058 74275058 TCCATTAAGGGACACTATGGCACGGGTTGGCAAACTTTTTCTGTAAAGGGCTAGGTAGTCTCTCT TCCATTAAGGGACACTATGGCACGGGTTGGCAGACTTTTTCTGTAAAGGGCTAGGTAGTCTCTCT T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1323495110 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3266074,Human_RBP_ID_3931875,Human_RBP_ID_5252511,Human_RBP_ID_8023567,Human_RBP_ID_16939686,Human_RBP_ID_21877138,Human_RBP_ID_24528033 RMVar_hsa_circ_335579,RMVar_hsa_circ_342788 27330 RMVar_ID_27330 Human_SNP_ID_721035540 A-to-I Human chrX - 74275355 74275355 74275355 TGAGATCTCATCTCTGCCAAAAAATAAAAATTAGCTGGGTGTGGTGGTGCATGGCTGTAGTCTCA TGAGATCTCATCTCTGCCAAAAAATAAAAATTCGCTGGGTGTGGTGGTGCATGGCTGTAGTCTCA T G FTX Ensembl:ENSG00000230590 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1332351186 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3932081,Human_RBP_ID_8278356,Human_RBP_ID_16939710,Human_RBP_ID_23106301 RMVar_hsa_circ_335579,RMVar_hsa_circ_342788 27331 RMVar_ID_27331 Human_SNP_ID_721035546 A-to-I Human chrX - 74275389 74275389 74275389 GCACAGGAGTTTGAGATCAGTCTGGGCAACGTAGTGAGATCTCATCTCTGCCAAAAAATAAAAAT GCACAGGAGTTTGAGATCAGTCTGGGCAACGTGGTGAGATCTCATCTCTGCCAAAAAATAAAAAT T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1425163445 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3932081,Human_RBP_ID_8023572,Human_RBP_ID_8278356,Human_RBP_ID_9249541,Human_RBP_ID_16939712,Human_RBP_ID_17580094,Human_RBP_ID_18154600,Human_RBP_ID_18924937,Human_RBP_ID_26295338 RMVar_hsa_circ_335579,RMVar_hsa_circ_342788 27332 RMVar_ID_27332 Human_SNP_ID_721035555 A-to-I Human chrX - 74275454 74275454 74275454 TGGTGGCTCGTGCCTGTAATCCCAACACTTTGAGAGGCTGAGGTGGGAGGATCGCTTGAGCTTGA TGGTGGCTCGTGCCTGTAATCCCAACACTTTGGGAGGCTGAGGTGGGAGGATCGCTTGAGCTTGA T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1049086372 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8023572,Human_RBP_ID_16939716 RMVar_hsa_circ_335579,RMVar_hsa_circ_342788 27333 RMVar_ID_27333 Human_SNP_ID_721035557 A-to-I Human chrX - 74275462 74275462 74275462 GTCGGATGTGGTGGCTCGTGCCTGTAATCCCAACACTTTGAGAGGCTGAGGTGGGAGGATCGCTT GTCGGATGTGGTGGCTCGTGCCTGTAATCCCAGCACTTTGAGAGGCTGAGGTGGGAGGATCGCTT T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE47997;GSE38233;GSE107867 K562 cells&HepG2 cells;cultured B-cells;ASD brains,Fragile X samples from NIH NeuroBioBank - 23474544,24183664,30559470 RNA-Seq:(High) rs1399043113 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8031418 RMVar_hsa_circ_335579,RMVar_hsa_circ_342788 27334 RMVar_ID_27334 Human_SNP_ID_721035645 A-to-I Human chrX - 74275970 74275970 74275970 CCTCGGCCTCCCAAAGTGGTGGGATTACAAGCATGAGCCACTGTGCCCTCCCTACAGGTTTTAAA CCTCGGCCTCCCAAAGTGGTGGGATTACAAGCGTGAGCCACTGTGCCCTCCCTACAGGTTTTAAA T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1280023987 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26295359 RMVar_hsa_circ_335579,RMVar_hsa_circ_342788 27335 RMVar_ID_27335 Human_SNP_ID_721035661 A-to-I Human chrX - 74276048 74276048 74276048 TTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTCACTGGGCTGGTCTCGAACTCCTGACCT TTTTGTATTTTTAGTAGAGACGGGGTTTCACCGTGTTCACTGGGCTGGTCTCGAACTCCTGACCT T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs753158109 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16939763 RMVar_hsa_circ_335579,RMVar_hsa_circ_342788 27336 RMVar_ID_27336 Human_SNP_ID_721035668 A-to-I Human chrX - 74276083 74276083 74276083 GGACTACAGGCGACCGCCATTACACTCAGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCA GGACTACAGGCGACCGCCATTACACTCAGCTAGTTTTTTGTATTTTTAGTAGAGACGGGGTTTCA T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1400397252 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_335579,RMVar_hsa_circ_342788 27337 RMVar_ID_27337 Human_SNP_ID_721035669 A-to-I Human chrX - 74276084 74276084 74276084 GGGACTACAGGCGACCGCCATTACACTCAGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTC GGGACTACAGGCGACCGCCATTACACTCAGCTGATTTTTTGTATTTTTAGTAGAGACGGGGTTTC T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs772210944 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_335579,RMVar_hsa_circ_342788 27338 RMVar_ID_27338 Human_SNP_ID_721035732 A-to-I Human chrX - 74276432 74276432 74276432 CTTGAGCCTGGGAGCTGAGATCGTGCCATTACACTCCAGTCTGGGTGACAGAGGGAAACTCTGTT CTTGAGCCTGGGAGCTGAGATCGTGCCATTACGCTCCAGTCTGGGTGACAGAGGGAAACTCTGTT T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1362617700 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3931501,Human_RBP_ID_16954946,Human_RBP_ID_26295368 RMVar_hsa_circ_335579,RMVar_hsa_circ_342788 27339 RMVar_ID_27339 Human_SNP_ID_721035738 A-to-I Human chrX - 74276468 74276468 74276468 ATTGCAGCTACTCAGGAGGCTGAAGTAGGAGAATCACTTGAGCCTGGGAGCTGAGATCGTGCCAT ATTGCAGCTACTCAGGAGGCTGAAGTAGGAGAGTCACTTGAGCCTGGGAGCTGAGATCGTGCCAT T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1174214121 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3931501 RMVar_hsa_circ_335579,RMVar_hsa_circ_342788 27340 RMVar_ID_27340 Human_SNP_ID_721035739 A-to-I Human chrX - 74276474 74276474 74276474 CCTGTAATTGCAGCTACTCAGGAGGCTGAAGTAGGAGAATCACTTGAGCCTGGGAGCTGAGATCG CCTGTAATTGCAGCTACTCAGGAGGCTGAAGTGGGAGAATCACTTGAGCCTGGGAGCTGAGATCG T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1478341900 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3931501,Human_RBP_ID_26295371 RMVar_hsa_circ_335579,RMVar_hsa_circ_342788 27341 RMVar_ID_27341 Human_SNP_ID_721035751 A-to-I Human chrX - 74276561 74276561 74276561 GTCAGGAGTTCGAGAGCAGCCTGGCCAACGTGATGAAACCCTGTCTCTACTAAAAATACAAAAAT GTCAGGAGTTCGAGAGCAGCCTGGCCAACGTGTTGAAACCCTGTCTCTACTAAAAATACAAAAAT T A FTX Ensembl:ENSG00000230590 lincRNA intron GSE47997;GSE38233;GSE100210;GSE107867 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;ASD brains,cerebellum - 23474544,24183664,29129909,30559470 RNA-Seq:(High) rs1222003902 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_335579,RMVar_hsa_circ_342788 27342 RMVar_ID_27342 Human_SNP_ID_721035834 A-to-I Human chrX - 74277106 74277106 74277106 TTTGTATTTTTTTGTAGAGACGGGGTTTTCCCATGTTGCCCAGGCTGGTCTCAAACTTCTGGACT TTTGTATTTTTTTGTAGAGACGGGGTTTTCCCGTGTTGCCCAGGCTGGTCTCAAACTTCTGGACT T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs989302736 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3931877,Human_RBP_ID_16967511 RMVar_hsa_circ_335579,RMVar_hsa_circ_342788 27343 RMVar_ID_27343 Human_SNP_ID_721035841 A-to-I Human chrX - 74277133 74277133 74277133 GCAAGCGCCACCATGCCCAGCTAATTTTTTGTATTTTTTTGTAGAGACGGGGTTTTCCCATGTTG GCAAGCGCCACCATGCCCAGCTAATTTTTTGTGTTTTTTTGTAGAGACGGGGTTTTCCCATGTTG T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs982228328 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_335579,RMVar_hsa_circ_342788 27344 RMVar_ID_27344 Human_SNP_ID_721035848 A-to-I Human chrX - 74277166 74277166 74277166 TCACCTCAACTTCCCGAGTAGTTGGGACTGCAAGCAAGCGCCACCATGCCCAGCTAATTTTTTGT TCACCTCAACTTCCCGAGTAGTTGGGACTGCAGGCAAGCGCCACCATGCCCAGCTAATTTTTTGT T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE38233;GSE100210;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 24183664,29129909,30559470 RNA-Seq:(High) rs916195191 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16939809 RMVar_hsa_circ_335579,RMVar_hsa_circ_342788 27345 RMVar_ID_27345 Human_SNP_ID_721035958 A-to-I Human chrX - 74277817 74277817 74277817 CTCCCTCCTCAGCCTCCCAAGTAGCTAGGACTACAGGATGCACCACCGTGCCCATTGTTTCTATA CTCCCTCCTCAGCCTCCCAAGTAGCTAGGACTGCAGGATGCACCACCGTGCCCATTGTTTCTATA T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs974068794 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8023606 RMVar_hsa_circ_335579,RMVar_hsa_circ_342788 27346 RMVar_ID_27346 Human_SNP_ID_721035960 A-to-I Human chrX - 74277823 74277823 74277823 ATAATCCTCCCTCCTCAGCCTCCCAAGTAGCTAGGACTACAGGATGCACCACCGTGCCCATTGTT ATAATCCTCCCTCCTCAGCCTCCCAAGTAGCTGGGACTACAGGATGCACCACCGTGCCCATTGTT T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1259402095 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8023606 RMVar_hsa_circ_335579,RMVar_hsa_circ_342788 27347 RMVar_ID_27347 Human_SNP_ID_721035961 A-to-I Human chrX - 74277830 74277830 74277830 GACTCAAATAATCCTCCCTCCTCAGCCTCCCAAGTAGCTAGGACTACAGGATGCACCACCGTGCC GACTCAAATAATCCTCCCTCCTCAGCCTCCCAGGTAGCTAGGACTACAGGATGCACCACCGTGCC T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs919956423 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_335579,RMVar_hsa_circ_342788 27348 RMVar_ID_27348 Human_SNP_ID_721035972 A-to-I Human chrX - 74277920 74277920 74277920 TGTTTCTTGTTTTTGAGACAGGGTCTTGCTCTATCTCCCAGGCTGGAGTGCAATGGTGCGATCAC TGTTTCTTGTTTTTGAGACAGGGTCTTGCTCTGTCTCCCAGGCTGGAGTGCAATGGTGCGATCAC T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs950981244 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16939862,Human_RBP_ID_23106311,Human_RBP_ID_26308617 RMVar_hsa_circ_335579,RMVar_hsa_circ_342788 27349 RMVar_ID_27349 Human_SNP_ID_721036095 A-to-I Human chrX - 74278481 74278479 74278481 AGGCGTGATAGCAGGCGCCTGTAGTTCCAGCTATGGGAGGCTGAGGCAGGAGAATCAGATGAACC AGGCGTGATAGCAGGCGCCTGTAGTTCCAGCT__GGGAGGCTGAGGCAGGAGAATCAGATGAACC CAT C FTX Ensembl:ENSG00000230590 lincRNA intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs999257431 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_8023620,Human_RBP_ID_17580095 RMVar_hsa_circ_335579,RMVar_hsa_circ_342788 27350 RMVar_ID_27350 Human_SNP_ID_721036096 A-to-I Human chrX - 74278481 74278481 74278481 AGGCGTGATAGCAGGCGCCTGTAGTTCCAGCTATGGGAGGCTGAGGCAGGAGAATCAGATGAACC AGGCGTGATAGCAGGCGCCTGTAGTTCCAGCTGTGGGAGGCTGAGGCAGGAGAATCAGATGAACC T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1200399457 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8023620,Human_RBP_ID_17580095 RMVar_hsa_circ_335579,RMVar_hsa_circ_342788 27351 RMVar_ID_27351 Human_SNP_ID_721036138 A-to-I Human chrX - 74278720 74278720 74278720 ACCTTGGGAGGCCGAGATGGGAGGATTGTGTGAGCCCAGGAGTTTGAGACCAGCCTGGGTAACAT ACCTTGGGAGGCCGAGATGGGAGGATTGTGTGGGCCCAGGAGTTTGAGACCAGCCTGGGTAACAT T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1454120859 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16939896,Human_RBP_ID_23317717 Human_miRNA_ID_3152372,Human_miRNA_ID_3176509,Human_miRNA_ID_3181681,Human_miRNA_ID_3182566,Human_miRNA_ID_3210224 RMVar_hsa_circ_335579,RMVar_hsa_circ_342788 27352 RMVar_ID_27352 Human_SNP_ID_721036148 A-to-I Human chrX - 74278765 74278765 74278765 CCCTTCTTCTCTGGGCAGGTGTGGTGGCTCCTACATTATCCCAGCACCTTGGGAGGCCGAGATGG CCCTTCTTCTCTGGGCAGGTGTGGTGGCTCCTGCATTATCCCAGCACCTTGGGAGGCCGAGATGG T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs174155 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8034525,Human_RBP_ID_16939900,Human_RBP_ID_21863801,Human_RBP_ID_22349828,Human_RBP_ID_23317718 Human_miRNA_ID_3158268,Human_miRNA_ID_3158359,Human_miRNA_ID_3190255,Human_miRNA_ID_3190902 GWAS_ID_2785,GWAS_ID_2786,GWAS_ID_2787,GWAS_ID_2788,GWAS_ID_2789,GWAS_ID_2790 RMVar_hsa_circ_335579,RMVar_hsa_circ_342788 27353 RMVar_ID_27353 Human_SNP_ID_721036219 A-to-I Human chrX - 74279189 74279189 74279189 CCAGACTGGTCTTGAACTCTTGGGCTCAAGCAATTCTTCCACCTCCGCCTCCCAAAGTGTTAGGA CCAGACTGGTCTTGAACTCTTGGGCTCAAGCATTTCTTCCACCTCCGCCTCCCAAAGTGTTAGGA T A FTX Ensembl:ENSG00000230590 lincRNA intron GSE100210;GSE107867 HepG2 cell line;ASD brains,temporal_cortex - 29129909,30559470 RNA-Seq:(High) rs1318861226 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3266095,Human_RBP_ID_3931503,Human_RBP_ID_5107832,Human_RBP_ID_5252348,Human_RBP_ID_8023631,Human_RBP_ID_10473545,Human_RBP_ID_16939935,Human_RBP_ID_26295436 RMVar_hsa_circ_335579,RMVar_hsa_circ_342788 27354 RMVar_ID_27354 Human_SNP_ID_721036612 A-to-I Human chrX - 74281727 74281727 74281727 TTGGGAGAGGCTCAAATCAGCATCCTGCACCTAGTTATCAAACCATTGTGAAGTCTTGGTAAGTG TTGGGAGAGGCTCAAATCAGCATCCTGCACCTGGTTATCAAACCATTGTGAAGTCTTGGTAAGTG T C FTX Ensembl:ENSG00000230590 lincRNA exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs174151 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5638408,Human_RBP_ID_9410044,Human_RBP_ID_19026815 Human_Splice_Rec_2218634,Human_Splice_Rec_2218644,Human_Splice_Rec_2218652,Human_Splice_Rec_2218671,Human_Splice_Rec_2218683,Human_Splice_Rec_2218699,Human_Splice_Rec_2218709,Human_Splice_Rec_2218722,Human_Splice_Rec_2218740,Human_Splice_Rec_2218748,Human_Splice_Rec_2218758,Human_Splice_Rec_2218768,Human_Splice_Rec_2218778,Human_Splice_Rec_2218786,Human_Splice_Rec_2218799,Human_Splice_Rec_2218808,Human_Splice_Rec_2218818,Human_Splice_Rec_2218826,Human_Splice_Rec_2218836,Human_Splice_Rec_2218846,Human_Splice_Rec_2218854,Human_Splice_Rec_2218868,Human_Splice_Rec_2218880,Human_Splice_Rec_2218892,Human_Splice_Rec_2218907,Human_Splice_Rec_2218925,Human_Splice_Rec_2218935,Human_Splice_Rec_2218945,Human_Splice_Rec_2218953,Human_Splice_Rec_2218963,Human_Splice_Rec_2218972,Human_Splice_Rec_2218982,Human_Splice_Rec_2218994,Human_Splice_Rec_2219004,Human_Splice_Rec_2219014,Human_Splice_Rec_2219024,Human_Splice_Rec_2219034,Human_Splice_Rec_2219044,Human_Splice_Rec_2219054,Human_Splice_Rec_2219062,Human_Splice_Rec_2219074,Human_Splice_Rec_2219084,Human_Splice_Rec_2219094,Human_Splice_Rec_2219103,Human_Splice_Rec_2219113,Human_Splice_Rec_2219123,Human_Splice_Rec_2219131,Human_Splice_Rec_2219145,Human_Splice_Rec_2219157,Human_Splice_Rec_2219165,Human_Splice_Rec_2219172,Human_Splice_Rec_2219180,Human_Splice_Rec_2219186,Human_Splice_Rec_2219192,Human_Splice_Rec_2219198,Human_Splice_Rec_2219206,Human_Splice_Rec_2219214,Human_Splice_Rec_2219219,Human_Splice_Rec_2219227 GWAS_ID_2791,GWAS_ID_2792,GWAS_ID_2793,GWAS_ID_2794,GWAS_ID_2795,GWAS_ID_2796 RMVar_hsa_circ_83953,RMVar_hsa_circ_342788,RMVar_hsa_circ_263043 27355 RMVar_ID_27355 Human_SNP_ID_721053063 A-to-I Human chrX - 74376200 74376200 74376200 AAGAGAATGAAGGAGGCTAAAGAGAAGCGCCAAGAACAAATTGCAAAGAGACACAGACTTTCTTC AAGAGAATGAAGGAGGCTAAAGAGAAGCGCCAGGAACAAATTGCAAAGAGACACAGACTTTCTTC T C AC004386.1 Ensembl:ENSG00000213269 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1407555222 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3266163,Human_RBP_ID_5073407,Human_RBP_ID_17443181,Human_RBP_ID_23106333,Human_RBP_ID_26575282,Human_RBP_ID_27151707 Human_miRNA_ID_1876050 27356 RMVar_ID_27356 Human_SNP_ID_721053066 A-to-I Human chrX - 74376212 74376212 74376212 AAACTTTTGGCCAAGAGAATGAAGGAGGCTAAAGAGAAGCGCCAAGAACAAATTGCAAAGAGACA AAACTTTTGGCCAAGAGAATGAAGGAGGCTAAGGAGAAGCGCCAAGAACAAATTGCAAAGAGACA T C AC004386.1 Ensembl:ENSG00000213269 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879214462 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5073408,Human_RBP_ID_17443181,Human_RBP_ID_26575283 Human_miRNA_ID_1912461 27357 RMVar_ID_27357 Human_SNP_ID_721089621 A-to-I Human chrX - 74580960 74580960 74580960 CTCCTTCCCTTAAAAAAAATTATATTTTTTTGAGACAGAGTCTCACTCTTGCCCAGGCTGGCATG CTCCTTCCCTTAAAAAAAATTATATTTTTTTGGGACAGAGTCTCACTCTTGCCCAGGCTGGCATG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs960268926 Functional Loss SNV dbSNP153 33..33 33 - - - 27358 RMVar_ID_27358 Human_SNP_ID_721090083 A-to-I Human chrX - 74583207 74583207 74583207 AGATTGATAATTCAGAACTTCTTCATATGCTCAAGTCTCCAGAGTCACTCCATTCTAAGGTTGAT AGATTGATAATTCAGAACTTCTTCATATGCTCGAGTCTCCAGAGTCACTCCATTCTAAGGTTGAT T C RLIM,PABPC1P3 Ensembl:ENSG00000131263,Ensembl:ENSG00000230673 Protein coding,Pseudogene 3'UTR,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879068026 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1886799,Human_miRNA_ID_1887661 27359 RMVar_ID_27359 Human_SNP_ID_498434553 A-to-I Human chr12 + 40726320 40726320 40726320 ATAAAAAGGATGTATTAGTTCATTCTCACACTACTATGAAGAAGTACCACACACTGGGTAATTTA ATAAAAAGGATGTATTAGTTCATTCTCACACTGCTATGAAGAAGTACCACACACTGGGTAATTTA A G CNTN1 Ensembl:ENSG00000018236 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1243577087 Functional Loss SNV dbSNP153 33..33 33 - - - 27360 RMVar_ID_27360 Human_SNP_ID_498440701 A-to-I Human chr12 + 40753658 40753658 40753658 TAACTGCTCCCATGATTCAGTTACCTCCCAATAGGTCCCTCCTATAACACGTGGGGATTATGGGA TAACTGCTCCCATGATTCAGTTACCTCCCAATGGGTCCCTCCTATAACACGTGGGGATTATGGGA A G CNTN1 Ensembl:ENSG00000018236 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1020252121 Functional Loss SNV dbSNP153 33..33 33 - - - 27361 RMVar_ID_27361 Human_SNP_ID_498441150 A-to-I Human chr12 + 40755479 40755479 40755479 GTCACATGATAATCCTAGTACTTTGGGAGGCTAAGGTGGGAGGATTGCTTGGGGCCGGGAGTTTG GTCACATGATAATCCTAGTACTTTGGGAGGCTGAGGTGGGAGGATTGCTTGGGGCCGGGAGTTTG A G CNTN1 Ensembl:ENSG00000018236 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1171427483 Functional Loss SNV dbSNP153 33..33 33 - - - 27362 RMVar_ID_27362 Human_SNP_ID_498456510 A-to-I Human chr12 + 40820081 40820081 40820081 GCTTATTATGTTTTTATAAGAAGCATGGCACTAGCAGCTGCATCTGGTAAAGGCCTCAGAATACT GCTTATTATGTTTTTATAAGAAGCATGGCACTGGCAGCTGCATCTGGTAAAGGCCTCAGAATACT A G CNTN1 Ensembl:ENSG00000018236 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs983795102 Functional Loss SNV dbSNP153 33..33 33 - - - 27363 RMVar_ID_27363 Human_SNP_ID_498773531 A-to-I Human chr12 - 42083956 42083956 42083956 TTTTTTTTTTAGTGGATCCCAGTTTGTGAGCTAGGACCTGTGGAAATACAAGTATCTTCCTTTTT TTTTTTTTTTAGTGGATCCCAGTTTGTGAGCTGGGACCTGTGGAAATACAAGTATCTTCCTTTTT T C GXYLT1 Ensembl:ENSG00000151233 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1338923625 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_418890,Human_RBP_ID_1268987,Human_RBP_ID_6179350,Human_RBP_ID_8780889,Human_RBP_ID_11931274,Human_RBP_ID_17684313,Human_RBP_ID_17818183 27364 RMVar_ID_27364 Human_SNP_ID_498774298 A-to-I Human chr12 - 42085672 42085672 42085672 AAAATCATCTTCTAGTTGGTTTGTTAGAATCAACAGAATATAAGTCACATGATGATTTCGTTTTT AAAATCATCTTCTAGTTGGTTTGTTAGAATCAGCAGAATATAAGTCACATGATGATTTCGTTTTT T C GXYLT1 Ensembl:ENSG00000151233 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1184072047 Functional Loss SNV dbSNP153 33..33 33 - - - 27365 RMVar_ID_27365 Human_SNP_ID_498784521 A-to-I Human chr12 - 42121444 42121444 42121444 TTGTGTGTGTGGATACTGGGTCTCGCTGTGTTACCCAGGTTGGTCTCAAACTCTGGGCCTCAAGC TTGTGTGTGTGGATACTGGGTCTCGCTGTGTTGCCCAGGTTGGTCTCAAACTCTGGGCCTCAAGC T C GXYLT1 Ensembl:ENSG00000151233 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs990062339 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_300486,RMVar_hsa_circ_155925,RMVar_hsa_circ_19755,RMVar_hsa_circ_155926,RMVar_hsa_circ_339721,RMVar_hsa_circ_155929,RMVar_hsa_circ_314421 27366 RMVar_ID_27366 Human_SNP_ID_498787747 A-to-I Human chr12 - 42134415 42134415 42134415 TCCTAGATACTTGGGGACTGAGGCAGGACGATAGCTTGAGCCCAGGAGATTGAGGCTGTAGTGAG TCCTAGATACTTGGGGACTGAGGCAGGACGATGGCTTGAGCCCAGGAGATTGAGGCTGTAGTGAG T C GXYLT1 Ensembl:ENSG00000151233 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs534176750 Functional Loss SNV dbSNP153 33..33 33 - - - 27367 RMVar_ID_27367 Human_SNP_ID_498801359 A-to-I Human chr12 - 42190243 42190243 42190243 GCTTCCCAGGCTCAAGAGATCATCCTTCCTCAACTTCCAAAGTATCTAGGACTACAGGCTCATGC GCTTCCCAGGCTCAAGAGATCATCCTTCCTCAGCTTCCAAAGTATCTAGGACTACAGGCTCATGC T C YAF2 Ensembl:ENSG00000015153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1308945190 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26611980 RMVar_hsa_circ_21111,RMVar_hsa_circ_155931,RMVar_hsa_circ_295616 27368 RMVar_ID_27368 Human_SNP_ID_498801718 A-to-I Human chr12 - 42191858 42191858 42191858 CTTGAACACTCCTGACCTCAAATGATCCTCCTACCTCAGCCTCCCAAACTGCTGGGATTACAGGC CTTGAACACTCCTGACCTCAAATGATCCTCCTGCCTCAGCCTCCCAAACTGCTGGGATTACAGGC T C YAF2 Ensembl:ENSG00000015153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404808065 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21111,RMVar_hsa_circ_155931,RMVar_hsa_circ_295616 27369 RMVar_ID_27369 Human_SNP_ID_498806092 A-to-I Human chr12 - 42210077 42210077 42210077 ATACATTTAGTTGGCCGGGCTTGCTGACTCACACTTGTAATCCCAGTACTTTTGGAGGCCAAGGC ATACATTTAGTTGGCCGGGCTTGCTGACTCACGCTTGTAATCCCAGTACTTTTGGAGGCCAAGGC T C YAF2 Ensembl:ENSG00000015153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs368459059 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11932166 RMVar_hsa_circ_21111,RMVar_hsa_circ_155932,RMVar_hsa_circ_155931,RMVar_hsa_circ_295616,RMVar_hsa_circ_306018,RMVar_hsa_circ_354678,RMVar_hsa_circ_155933 27370 RMVar_ID_27370 Human_SNP_ID_498808981 A-to-I Human chr12 - 42222463 42222463 42222463 TATGGCTGGTGAGGAAGATGGTCCGCTAGTCAAATAATTAATGTTAGAGCCTAGATTGAAACCTG TATGGCTGGTGAGGAAGATGGTCCGCTAGTCAGATAATTAATGTTAGAGCCTAGATTGAAACCTG T C YAF2 Ensembl:ENSG00000015153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1460620683 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24967442 27371 RMVar_ID_27371 Human_SNP_ID_498809005 A-to-I Human chr12 - 42222528 42222528 42222528 AGTGCTTTACTGTGTTCAGAGTGCTTTCCTATATATCCTTCTATTTGCTCATCAAACCGCCCCTA AGTGCTTTACTGTGTTCAGAGTGCTTTCCTATGTATCCTTCTATTTGCTCATCAAACCGCCCCTA T C YAF2 Ensembl:ENSG00000015153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1426519903 Functional Loss SNV dbSNP153 33..33 33 - - - 27372 RMVar_ID_27372 Human_SNP_ID_498809182 A-to-I Human chr12 - 42223178 42223178 42223178 ATAAGCAAAGAAACCTTTCACCCAACTATGATAGTTTTATAAACCTCTTTCAAACAACTCGGGTG ATAAGCAAAGAAACCTTTCACCCAACTATGATGGTTTTATAAACCTCTTTCAAACAACTCGGGTG T C YAF2 Ensembl:ENSG00000015153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1345627330 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11932371 27373 RMVar_ID_27373 Human_SNP_ID_498810047 A-to-I Human chr12 - 42226419 42226419 42226419 GGGCCAAAGCAATCCTCTCACCTTGGCCTCCAAAATGTTGGGATTACAGGCATGAACCACTGCAC GGGCCAAAGCAATCCTCTCACCTTGGCCTCCATAATGTTGGGATTACAGGCATGAACCACTGCAC T A YAF2 Ensembl:ENSG00000015153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs528341505 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17561367 27374 RMVar_ID_27374 Human_SNP_ID_498810048 A-to-I Human chr12 - 42226419 42226419 42226419 GGGCCAAAGCAATCCTCTCACCTTGGCCTCCAAAATGTTGGGATTACAGGCATGAACCACTGCAC GGGCCAAAGCAATCCTCTCACCTTGGCCTCCAGAATGTTGGGATTACAGGCATGAACCACTGCAC T C YAF2 Ensembl:ENSG00000015153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs528341505 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17561367 27375 RMVar_ID_27375 Human_SNP_ID_498812510 A-to-I Human chr12 - 42234088 42234088 42234088 CGGCTCACTGCAACCTCCACCTCCCAGGTTCAAGCAATTCTCATGCCTCAGCCTCTGTGGTAGCT CGGCTCACTGCAACCTCCACCTCCCAGGTTCAGGCAATTCTCATGCCTCAGCCTCTGTGGTAGCT T C YAF2 Ensembl:ENSG00000015153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs914404581 Functional Loss SNV dbSNP153 33..33 33 - - - 27376 RMVar_ID_27376 Human_SNP_ID_498842714 A-to-I Human chr12 + 42352619 42352619 42352619 TTCAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGACATCAAGTGGGA TTCAGTAGAGACAGGGTTTCACCATGTTGGCCGGGCTGGTCTTGAACTCCTGACATCAAGTGGGA A G PPHLN1 Ensembl:ENSG00000134283 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1333935657 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23157447 RMVar_hsa_circ_8748,RMVar_hsa_circ_155943,RMVar_hsa_circ_93526,RMVar_hsa_circ_97762,RMVar_hsa_circ_155944,RMVar_hsa_circ_346863,RMVar_hsa_circ_355560,RMVar_hsa_circ_109108,RMVar_hsa_circ_274665,RMVar_hsa_circ_303749,RMVar_hsa_circ_271102,RMVar_hsa_circ_36527,RMVar_hsa_circ_155948,RMVar_hsa_circ_155949,RMVar_hsa_circ_155950,RMVar_hsa_circ_155947 27377 RMVar_ID_27377 Human_SNP_ID_498844477 A-to-I Human chr12 + 42359997 42359997 42359997 AGGCATGGTGGCAAACACCTGTAGTCCCAGCTACTCGGGAGGCTGAAGCAGGAGAATCACTTGAA AGGCATGGTGGCAAACACCTGTAGTCCCAGCTGCTCGGGAGGCTGAAGCAGGAGAATCACTTGAA A G PPHLN1 Ensembl:ENSG00000134283 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1488612331 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8748,RMVar_hsa_circ_155943,RMVar_hsa_circ_93526,RMVar_hsa_circ_97762,RMVar_hsa_circ_155944,RMVar_hsa_circ_346863,RMVar_hsa_circ_355560,RMVar_hsa_circ_109108,RMVar_hsa_circ_274665,RMVar_hsa_circ_271102,RMVar_hsa_circ_36527,RMVar_hsa_circ_301317,RMVar_hsa_circ_155948,RMVar_hsa_circ_155949,RMVar_hsa_circ_155950,RMVar_hsa_circ_319569,RMVar_hsa_circ_311443,RMVar_hsa_circ_155952,RMVar_hsa_circ_282377,RMVar_hsa_circ_155951 27378 RMVar_ID_27378 Human_SNP_ID_498844486 A-to-I Human chr12 + 42360033 42360033 42360033 GGGAGGCTGAAGCAGGAGAATCACTTGAACTCAGGAGATGGAGGCTGCAGTGAGCTGAGTTCACC GGGAGGCTGAAGCAGGAGAATCACTTGAACTCGGGAGATGGAGGCTGCAGTGAGCTGAGTTCACC A G PPHLN1 Ensembl:ENSG00000134283 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1338909871 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11933228 RMVar_hsa_circ_8748,RMVar_hsa_circ_155943,RMVar_hsa_circ_93526,RMVar_hsa_circ_97762,RMVar_hsa_circ_155944,RMVar_hsa_circ_346863,RMVar_hsa_circ_355560,RMVar_hsa_circ_109108,RMVar_hsa_circ_274665,RMVar_hsa_circ_271102,RMVar_hsa_circ_36527,RMVar_hsa_circ_301317,RMVar_hsa_circ_155948,RMVar_hsa_circ_155949,RMVar_hsa_circ_155950,RMVar_hsa_circ_319569,RMVar_hsa_circ_311443,RMVar_hsa_circ_155952,RMVar_hsa_circ_282377,RMVar_hsa_circ_155951 27379 RMVar_ID_27379 Human_SNP_ID_498844729 A-to-I Human chr12 + 42360634 42360634 42360634 TCCCCTGCCTCAGCCTCCAAGTAGCTGGGACTACAGGCGTGTGCCACCACCGCTGGCTAATTTTT TCCCCTGCCTCAGCCTCCAAGTAGCTGGGACTGCAGGCGTGTGCCACCACCGCTGGCTAATTTTT A G PPHLN1 Ensembl:ENSG00000134283 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909525395 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8748,RMVar_hsa_circ_155943,RMVar_hsa_circ_93526,RMVar_hsa_circ_97762,RMVar_hsa_circ_155944,RMVar_hsa_circ_346863,RMVar_hsa_circ_355560,RMVar_hsa_circ_109108,RMVar_hsa_circ_274665,RMVar_hsa_circ_271102,RMVar_hsa_circ_36527,RMVar_hsa_circ_301317,RMVar_hsa_circ_155948,RMVar_hsa_circ_155949,RMVar_hsa_circ_155950,RMVar_hsa_circ_319569,RMVar_hsa_circ_311443,RMVar_hsa_circ_155952,RMVar_hsa_circ_282377,RMVar_hsa_circ_155951 27380 RMVar_ID_27380 Human_SNP_ID_498844743 A-to-I Human chr12 + 42360660 42360660 42360660 GGGACTACAGGCGTGTGCCACCACCGCTGGCTAATTTTTGTATTTTTAGTAGAGACGAGGTTTCA GGGACTACAGGCGTGTGCCACCACCGCTGGCTTATTTTTGTATTTTTAGTAGAGACGAGGTTTCA A T PPHLN1 Ensembl:ENSG00000134283 Protein coding intron GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831 HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line - 29129909,32596459 RNA-Seq:(High) rs1447663243 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8748,RMVar_hsa_circ_155943,RMVar_hsa_circ_93526,RMVar_hsa_circ_97762,RMVar_hsa_circ_155944,RMVar_hsa_circ_346863,RMVar_hsa_circ_355560,RMVar_hsa_circ_109108,RMVar_hsa_circ_274665,RMVar_hsa_circ_271102,RMVar_hsa_circ_36527,RMVar_hsa_circ_301317,RMVar_hsa_circ_155948,RMVar_hsa_circ_155949,RMVar_hsa_circ_155950,RMVar_hsa_circ_319569,RMVar_hsa_circ_311443,RMVar_hsa_circ_155952,RMVar_hsa_circ_282377,RMVar_hsa_circ_155951 27381 RMVar_ID_27381 Human_SNP_ID_498844757 A-to-I Human chr12 + 42360723 42360723 42360723 CATTATGTTGGCCAGGCTGCTCTTGAACTCCTAACCTCGTGATCTGCCCACCTTGGCCTCCCAAA CATTATGTTGGCCAGGCTGCTCTTGAACTCCTGACCTCGTGATCTGCCCACCTTGGCCTCCCAAA A G PPHLN1 Ensembl:ENSG00000134283 Protein coding intron GSE100210;GSE99789;GSE123020:GSM3490829,GSM3490830,GSM3490831 HepG2 cell line;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109 cell line - 29129909,29796672,32596459 RNA-Seq:(High) rs923445977 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8748,RMVar_hsa_circ_155943,RMVar_hsa_circ_93526,RMVar_hsa_circ_97762,RMVar_hsa_circ_155944,RMVar_hsa_circ_346863,RMVar_hsa_circ_355560,RMVar_hsa_circ_109108,RMVar_hsa_circ_274665,RMVar_hsa_circ_271102,RMVar_hsa_circ_36527,RMVar_hsa_circ_301317,RMVar_hsa_circ_155948,RMVar_hsa_circ_155949,RMVar_hsa_circ_155950,RMVar_hsa_circ_319569,RMVar_hsa_circ_311443,RMVar_hsa_circ_155952,RMVar_hsa_circ_282377,RMVar_hsa_circ_155951 27382 RMVar_ID_27382 Human_SNP_ID_498855050 A-to-I Human chr12 + 42401878 42401878 42401878 TGTTGTTTGTTTATTTGTTTGTTTTTTGAGACAGGGTCTTACTCTGTCGCCCATGCTGGAGTGCA TGTTGTTTGTTTATTTGTTTGTTTTTTGAGACGGGGTCTTACTCTGTCGCCCATGCTGGAGTGCA A G PPHLN1 Ensembl:ENSG00000134283 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1165276783 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24967889 RMVar_hsa_circ_109108,RMVar_hsa_circ_155950 27383 RMVar_ID_27383 Human_SNP_ID_498862634 A-to-I Human chr12 + 42432333 42432333 42432333 AATCTGTTATGGCTGCTCATTAATCTGTAGGCATTCCATTCTTAGCTGTTCTACTTCCTTTAGAT AATCTGTTATGGCTGCTCATTAATCTGTAGGCGTTCCATTCTTAGCTGTTCTACTTCCTTTAGAT A G PPHLN1 Ensembl:ENSG00000134283 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1419350739 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18625904 RMVar_hsa_circ_109108,RMVar_hsa_circ_155950 27384 RMVar_ID_27384 Human_SNP_ID_498862640 A-to-I Human chr12 + 42432366 42432366 42432366 TTCCATTCTTAGCTGTTCTACTTCCTTTAGATAAGCAATATGGTACTCTAAAAGAACTTGCACAT TTCCATTCTTAGCTGTTCTACTTCCTTTAGATGAGCAATATGGTACTCTAAAAGAACTTGCACAT A G PPHLN1 Ensembl:ENSG00000134283 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965440725 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109108,RMVar_hsa_circ_155950 27385 RMVar_ID_27385 Human_SNP_ID_498862645 A-to-I Human chr12 + 42432383 42432383 42432383 CTACTTCCTTTAGATAAGCAATATGGTACTCTAAAAGAACTTGCACATTTCCAATGGTTTCTTTA CTACTTCCTTTAGATAAGCAATATGGTACTCTGAAAGAACTTGCACATTTCCAATGGTTTCTTTA A G PPHLN1 Ensembl:ENSG00000134283 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs185315011 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11934683 RMVar_hsa_circ_109108,RMVar_hsa_circ_155950 27386 RMVar_ID_27386 Human_SNP_ID_498862655 A-to-I Human chr12 - 42432438 42432438 42432438 GTGAAAATAAACTACCCAGAGAAGACAGTATGATTCCATTTGTATTTGTTGGCACTAAAGAAACC GTGAAAATAAACTACCCAGAGAAGACAGTATGGTTCCATTTGTATTTGTTGGCACTAAAGAAACC T C AC079601.3 Ensembl:ENSG00000257376 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1367547445 Functional Loss SNV dbSNP153 33..33 33 - - - 27387 RMVar_ID_27387 Human_SNP_ID_498862658 A-to-I Human chr12 - 42432444 42432444 42432444 GGGACAGTGAAAATAAACTACCCAGAGAAGACAGTATGATTCCATTTGTATTTGTTGGCACTAAA GGGACAGTGAAAATAAACTACCCAGAGAAGACGGTATGATTCCATTTGTATTTGTTGGCACTAAA T C AC079601.3 Ensembl:ENSG00000257376 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1446261355 Functional Loss SNV dbSNP153 33..33 33 - - - 27388 RMVar_ID_27388 Human_SNP_ID_498862688 A-to-I Human chr12 - 42432558 42432558 42432558 TGGAGGATTTTATTCAGGTTTCTAAGAATCTCACTGGAAAAGTAATTGGAAAAAATGGCAAAGTT TGGAGGATTTTATTCAGGTTTCTAAGAATCTCGCTGGAAAAGTAATTGGAAAAAATGGCAAAGTT T C AC079601.3 Ensembl:ENSG00000257376 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1374735687 Functional Loss SNV dbSNP153 33..33 33 - - - 27389 RMVar_ID_27389 Human_SNP_ID_498862691 A-to-I Human chr12 - 42432566 42432566 42432566 GGAATTTGTGGAGGATTTTATTCAGGTTTCTAAGAATCTCACTGGAAAAGTAATTGGAAAAAATG GGAATTTGTGGAGGATTTTATTCAGGTTTCTAGGAATCTCACTGGAAAAGTAATTGGAAAAAATG T C AC079601.3 Ensembl:ENSG00000257376 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs531918527 Functional Loss SNV dbSNP153 33..33 33 - - - 27390 RMVar_ID_27390 Human_SNP_ID_498862693 A-to-I Human chr12 + 42432570 42432570 42432570 TTTTCCAATTACTTTTCCAGTGAGATTCTTAGAAACCTGAATAAAATCCTCCACAAATTCCAAGA TTTTCCAATTACTTTTCCAGTGAGATTCTTAGGAACCTGAATAAAATCCTCCACAAATTCCAAGA A G PPHLN1 Ensembl:ENSG00000134283 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs549890660 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3404614,Human_RBP_ID_8375017 RMVar_hsa_circ_109108,RMVar_hsa_circ_155950 27391 RMVar_ID_27391 Human_SNP_ID_499191296 A-to-I Human chr12 + 43787879 43787879 43787879 AAGAGTTCAAGACCGGCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAG AAGAGTTCAAGACCGGCCTGGCCAACATGGTGGAACCCCGTCTCTACTAAAAATACAAAAATTAG A G IRAK4 Ensembl:ENSG00000198001 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs974243476 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_117077 27392 RMVar_ID_27392 Human_SNP_ID_499191312 A-to-I Human chr12 + 43787942 43787942 43787942 AGACGAGCGTGGTGGTGGACACCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGACTAGCT AGACGAGCGTGGTGGTGGACACCTGTAGTCCCGGCTACTTGGGAGGCTGAGGCAGGAGACTAGCT A G IRAK4 Ensembl:ENSG00000198001 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167046982 Functional Loss SNV dbSNP153 33..33 33 - - - 27393 RMVar_ID_27393 Human_SNP_ID_499191316 A-to-I Human chr12 + 43787998 43787998 43787998 AGACTAGCTGGAACCAGGGAGGTAGAGGTTGCAGTGAGCTGAGATCGTGCCACTGCACTCCAGCC AGACTAGCTGGAACCAGGGAGGTAGAGGTTGCGGTGAGCTGAGATCGTGCCACTGCACTCCAGCC A G IRAK4 Ensembl:ENSG00000198001 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1457063703 Functional Loss SNV dbSNP153 33..33 33 - - - 27394 RMVar_ID_27394 Human_SNP_ID_499191319 A-to-I Human chr12 + 43788009 43788009 43788009 AACCAGGGAGGTAGAGGTTGCAGTGAGCTGAGATCGTGCCACTGCACTCCAGCCTGGGTGACAGA AACCAGGGAGGTAGAGGTTGCAGTGAGCTGAGGTCGTGCCACTGCACTCCAGCCTGGGTGACAGA A G IRAK4 Ensembl:ENSG00000198001 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs933500132 Functional Loss SNV dbSNP153 33..33 33 - - - 27395 RMVar_ID_27395 Human_SNP_ID_499229534 A-to-I Human chr12 + 43945557 43945557 43945557 GTTGGTTCGTCTGGTCTCGAATTCCTGACCTCAGGTGATCCACCCGCTTTGGCCTCCCAAAGTGC GTTGGTTCGTCTGGTCTCGAATTCCTGACCTCGGGTGATCCACCCGCTTTGGCCTCCCAAAGTGC A G TMEM117 Ensembl:ENSG00000139173 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170595093 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50125 27396 RMVar_ID_27396 Human_SNP_ID_499230472 A-to-I Human chr12 + 43949597 43949597 43949597 ACTTCTGAGATCTTGTCGGGAAGCTGCTGATCACCAAGAGTTTGCTATCTGTTGGGAGACTGCCT ACTTCTGAGATCTTGTCGGGAAGCTGCTGATCGCCAAGAGTTTGCTATCTGTTGGGAGACTGCCT A G TMEM117 Ensembl:ENSG00000139173 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1441489084 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50125 27397 RMVar_ID_27397 Human_SNP_ID_499230693 A-to-I Human chr12 + 43950671 43950671 43950671 AGCAAATTCCTGGTGATCAGCAGCTTCCCGATAAGCTCTCAGAAGTTGGGCTAGTGGGCTCAAGC AGCAAATTCCTGGTGATCAGCAGCTTCCCGATCAGCTCTCAGAAGTTGGGCTAGTGGGCTCAAGC A C TMEM117 Ensembl:ENSG00000139173 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs865829976 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50125 27398 RMVar_ID_27398 Human_SNP_ID_499230696 A-to-I Human chr12 + 43950679 43950679 43950679 CCTGGTGATCAGCAGCTTCCCGATAAGCTCTCAGAAGTTGGGCTAGTGGGCTCAAGCATGTGCAC CCTGGTGATCAGCAGCTTCCCGATAAGCTCTCCGAAGTTGGGCTAGTGGGCTCAAGCATGTGCAC A C TMEM117 Ensembl:ENSG00000139173 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1220977789 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50125 27399 RMVar_ID_27399 Human_SNP_ID_499234573 A-to-I Human chr12 + 43967196 43967196 43967196 TCACCCAGTTTGGAATGCGATGGCGCAGTCACAGCTCACTACAGCCTTGACCTCCTGCTCAAATG TCACCCAGTTTGGAATGCGATGGCGCAGTCACGGCTCACTACAGCCTTGACCTCCTGCTCAAATG A G TMEM117 Ensembl:ENSG00000139173 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs894702500 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50125 27400 RMVar_ID_27400 Human_SNP_ID_499314620 A-to-I Human chr12 + 44308826 44308826 44308826 TATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGTCAGGATGGTCTCGATCTCCTGACGTCGTGA TATTTTTAGTAGAGACGGGGTTTCACCGTGTTGGTCAGGATGGTCTCGATCTCCTGACGTCGTGA A G TMEM117 Ensembl:ENSG00000139173 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1443517497 Functional Loss SNV dbSNP153 33..33 33 - - - 27401 RMVar_ID_27401 Human_SNP_ID_499526972 A-to-I Human chr12 + 45174536 45174536 45174536 ATACTGTTCCCCGGGGATTATCAGGTCCATGCATGTATTATCTACAGAATGAACTTCAATTTCAC ATACTGTTCCCCGGGGATTATCAGGTCCATGCGTGTATTATCTACAGAATGAACTTCAATTTCAC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913431289 Functional Loss SNV dbSNP153 33..33 33 - - - 27402 RMVar_ID_27402 Human_SNP_ID_499545821 A-to-I Human chr12 + 45250612 45250612 45250612 TGTTGTTGAGGGGTCGTCTTGCTGTGTTGCCTAGGCTGGTCTCAAATTTCTGACCTCAAGTGATC TGTTGTTGAGGGGTCGTCTTGCTGTGTTGCCTGGGCTGGTCTCAAATTTCTGACCTCAAGTGATC A G ANO6 Ensembl:ENSG00000177119 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1195200951 Functional Loss SNV dbSNP153 33..33 33 - - - 27403 RMVar_ID_27403 Human_SNP_ID_499557342 A-to-I Human chr12 + 45300230 45300230 45300230 TTGAGACAGAATCTTGCTCTGTCACCCAGGCTAGAGTGCAGCTGCATGATCACAGTCACTGTAGC TTGAGACAGAATCTTGCTCTGTCACCCAGGCTGGAGTGCAGCTGCATGATCACAGTCACTGTAGC A G ANO6 Ensembl:ENSG00000177119 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1196704344 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26579,RMVar_hsa_circ_5563 27404 RMVar_ID_27404 Human_SNP_ID_499663194 A-to-I Human chr12 + 45752655 45752655 45752655 GCAGTCCTTCTGCCTCACTCTCCTGAGTAGCTAGGACTCAGACTCATACCACCACACCCAGCTGA GCAGTCCTTCTGCCTCACTCTCCTGAGTAGCTGGGACTCAGACTCATACCACCACACCCAGCTGA A G ARID2 Ensembl:ENSG00000189079 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1441858667 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114716,RMVar_hsa_circ_33444,RMVar_hsa_circ_156046 27405 RMVar_ID_27405 Human_SNP_ID_499663483 A-to-I Human chr12 + 45753777 45753777 45753777 CACCATGCCTGGCTAATTTTTGTATTTTTTGTAGAGACGAGGTCTCCCTGTGTTGCTCAGGCTGG CACCATGCCTGGCTAATTTTTGTATTTTTTGTGGAGACGAGGTCTCCCTGTGTTGCTCAGGCTGG A G ARID2 Ensembl:ENSG00000189079 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1395571497 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11939042 RMVar_hsa_circ_114716,RMVar_hsa_circ_33444,RMVar_hsa_circ_156046 27406 RMVar_ID_27406 Human_SNP_ID_499663982 A-to-I Human chr12 + 45756005 45756005 45756005 TCGGCTCACTGCAACCTCTGCCTCCCAGGTTCAAGCGATTTTCGTGCCTCAGCCTCCGGAGTAGC TCGGCTCACTGCAACCTCTGCCTCCCAGGTTCGAGCGATTTTCGTGCCTCAGCCTCCGGAGTAGC A G ARID2 Ensembl:ENSG00000189079 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1248782445 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1358308 RMVar_hsa_circ_114716,RMVar_hsa_circ_33444,RMVar_hsa_circ_156046 27407 RMVar_ID_27407 Human_SNP_ID_499668657 A-to-I Human chr12 + 45776692 45776692 45776692 AAAATCGAGGCTGGGCATGGTGGATCATGCCTATAATCCCAGCACTTTGGGAGGCCAAGGCGGAC AAAATCGAGGCTGGGCATGGTGGATCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGAC A G ARID2 Ensembl:ENSG00000189079 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1377682283 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114716,RMVar_hsa_circ_33444,RMVar_hsa_circ_156046 27408 RMVar_ID_27408 Human_SNP_ID_499672477 A-to-I Human chr12 + 45793206 45793206 45793206 CCTATAATCCCAGTTACTTGGGAGGCTGAGACAAGAGAACCGCTTGAACCCCGGAAGCAGAGGTT CCTATAATCCCAGTTACTTGGGAGGCTGAGACGAGAGAACCGCTTGAACCCCGGAAGCAGAGGTT A G ARID2 Ensembl:ENSG00000189079 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs938916338 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11939560 RMVar_hsa_circ_114716,RMVar_hsa_circ_33444,RMVar_hsa_circ_156046 27409 RMVar_ID_27409 Human_SNP_ID_499680337 A-to-I Human chr12 + 45826469 45826469 45826469 TTTGAGACAGTCTTACTCTTATCACCCAGGCTAGAGTCCAGTGGTGCCATTGTAGTTCATTGCAA TTTGAGACAGTCTTACTCTTATCACCCAGGCTGGAGTCCAGTGGTGCCATTGTAGTTCATTGCAA A G ARID2 Ensembl:ENSG00000189079 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs938055264 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_303407,RMVar_hsa_circ_321681,RMVar_hsa_circ_363903,RMVar_hsa_circ_68847,RMVar_hsa_circ_156052,RMVar_hsa_circ_156053,RMVar_hsa_circ_126501 27410 RMVar_ID_27410 Human_SNP_ID_499684464 A-to-I Human chr12 + 45844167 45844167 45844167 TCAATCGATCCCCCTACCTCAGGCTCCTGAGTAGTTGGTACTACAAGTACATGCCACCAAGTCTG TCAATCGATCCCCCTACCTCAGGCTCCTGAGTCGTTGGTACTACAAGTACATGCCACCAAGTCTG A C ARID2 Ensembl:ENSG00000189079 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1565619043 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10458,RMVar_hsa_circ_11427,RMVar_hsa_circ_303407,RMVar_hsa_circ_363903,RMVar_hsa_circ_68847,RMVar_hsa_circ_293483,RMVar_hsa_circ_327759,RMVar_hsa_circ_312092,RMVar_hsa_circ_69412,RMVar_hsa_circ_88125,RMVar_hsa_circ_156056,RMVar_hsa_circ_156057,RMVar_hsa_circ_156058,RMVar_hsa_circ_108547,RMVar_hsa_circ_65605,RMVar_hsa_circ_59883,RMVar_hsa_circ_156059,RMVar_hsa_circ_156060,RMVar_hsa_circ_69773,RMVar_hsa_circ_156062,RMVar_hsa_circ_127224 27411 RMVar_ID_27411 Human_SNP_ID_499687983 A-to-I Human chr12 + 45857839 45857839 45857839 TGGAGTGCAGTGGCACACTCTTGGCTCACTGCAACCTCTGCCTCTTGGGCTTAAGCAATCCTCCT TGGAGTGCAGTGGCACACTCTTGGCTCACTGCTACCTCTGCCTCTTGGGCTTAAGCAATCCTCCT A T ARID2 Ensembl:ENSG00000189079 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs747024114 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10458,RMVar_hsa_circ_303407,RMVar_hsa_circ_363903,RMVar_hsa_circ_293483,RMVar_hsa_circ_312092,RMVar_hsa_circ_88125,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_156063 27412 RMVar_ID_27412 Human_SNP_ID_499698060 A-to-I Human chr12 + 45900084 45900083 45900085 TCTTTCTCTTTTTTATTTTTATTTTTTGAGACAGAGTCTCGCTCTGTCACCCAGACTGGAGTTCC TCTTTCTCTTTTTTATTTTTATTTTTTGAGAC__AGTCTCGCTCTGTCACCCAGACTGGAGTTCC CAG C ARID2 Ensembl:ENSG00000189079 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs531998378 Functional Loss DEL dbSNP153 33..34 33 - - - 27413 RMVar_ID_27413 Human_SNP_ID_499699462 A-to-I Human chr12 - 45905762 45905762 45905762 AGAAAACTTTAGAACCTACCAATAATGCTTCTAGGACACCACAGAATGTATTTCCAGTGGCTGCA AGAAAACTTTAGAACCTACCAATAATGCTTCTGGGACACCACAGAATGTATTTCCAGTGGCTGCA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs768404155 Functional Loss SNV dbSNP153 33..33 33 - - - 27414 RMVar_ID_27414 Human_SNP_ID_499707042 A-to-I Human chr12 - 45936306 45936306 45936306 GAAACCCCATCTCTACTAAAAATACCAAAATTAGCCGGGCGTGGTGGTGTGCGCCTGTAGTCCCA GAAACCCCATCTCTACTAAAAATACCAAAATTGGCCGGGCGTGGTGGTGTGCGCCTGTAGTCCCA T C SCAF11 Ensembl:ENSG00000139218 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1172845621 Functional Loss SNV dbSNP153 33..33 33 - - - 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 27415 RMVar_ID_27415 Human_SNP_ID_499711146 A-to-I Human chr12 - 45954654 45954654 45954654 AAGTGGAAGAATTGCTTGAGCCCCAGGAGTTCAAGCCTGCAGTAAGCTGTGATCAGGTGACTGCA AAGTGGAAGAATTGCTTGAGCCCCAGGAGTTCGAGCCTGCAGTAAGCTGTGATCAGGTGACTGCA T C SCAF11 Ensembl:ENSG00000139218 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1435394000 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24970931 RMVar_hsa_circ_57537,RMVar_hsa_circ_156078,RMVar_hsa_circ_59832,RMVar_hsa_circ_336950,RMVar_hsa_circ_357848,RMVar_hsa_circ_156082,RMVar_hsa_circ_354258,RMVar_hsa_circ_63793 27416 RMVar_ID_27416 Human_SNP_ID_499711358 A-to-I Human chr12 - 45955209 45955209 45955209 GAGGTTGCAGTGAGCCGTGATGCCGCTGCACTACAGCCTGGGCAAGAGGGTGAGACCCTGTTTAA GAGGTTGCAGTGAGCCGTGATGCCGCTGCACTGCAGCCTGGGCAAGAGGGTGAGACCCTGTTTAA T C SCAF11 Ensembl:ENSG00000139218 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1372165862 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24970940 RMVar_hsa_circ_57537,RMVar_hsa_circ_156078,RMVar_hsa_circ_59832,RMVar_hsa_circ_336950,RMVar_hsa_circ_357848,RMVar_hsa_circ_156082,RMVar_hsa_circ_354258,RMVar_hsa_circ_63793,RMVar_hsa_circ_156084,RMVar_hsa_circ_109068 27417 RMVar_ID_27417 Human_SNP_ID_499717714 A-to-I Human chr12 - 45980764 45980764 45980764 TTTGCACTAAAAGGGCATGAGAGTCACTCACTAAATAGAGCTAATTTAAGAGAATGGAACATAGA TTTGCACTAAAAGGGCATGAGAGTCACTCACTCAATAGAGCTAATTTAAGAGAATGGAACATAGA T G SCAF11 Ensembl:ENSG00000139218 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs972396192 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11941907 27418 RMVar_ID_27418 Human_SNP_ID_499769419 A-to-I Human chr12 - 46185606 46185606 46185606 GCCCTGCCCACCACAGAAAAGGATGCTGCTGCATAGCTTCTCCAATGTACCAGTCATTGAGGCCA GCCCTGCCCACCACAGAAAAGGATGCTGCTGCTTAGCTTCTCCAATGTACCAGTCATTGAGGCCA T A SLC38A1 Ensembl:ENSG00000111371 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs533005485 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4222281,Human_RBP_ID_17684424,Human_RBP_ID_22383132,Human_RBP_ID_26415813 Human_miRNA_ID_204040 RMVar_hsa_circ_156085,RMVar_hsa_circ_105387 27419 RMVar_ID_27419 Human_SNP_ID_499790589 A-to-I Human chr12 + 46273127 46273127 46273127 CCACGCTCCTGCCTCGGCCTCCCAAAAATACTAGGATTACAGGCCTGAACCACCATACCTGACCC CCACGCTCCTGCCTCGGCCTCCCAAAAATACTGGGATTACAGGCCTGAACCACCATACCTGACCC A G lnc-ARID2-8 RNACentral:URS00008BCCFF lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048934712 Functional Loss SNV dbSNP153 33..33 33 - - - 27420 RMVar_ID_27420 Human_SNP_ID_499790592 A-to-I Human chr12 + 46273135 46273135 46273135 CTGCCTCGGCCTCCCAAAAATACTAGGATTACAGGCCTGAACCACCATACCTGACCCGAGATGCT CTGCCTCGGCCTCCCAAAAATACTAGGATTACGGGCCTGAACCACCATACCTGACCCGAGATGCT A G lnc-ARID2-8 RNACentral:URS00008BCCFF lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1204380936 Functional Loss SNV dbSNP153 33..33 33 - - - 27421 RMVar_ID_27421 Human_SNP_ID_499818083 A-to-I Human chr12 - 46370665 46370665 46370665 ACTTGCCCAAAGCTGGTTTTCTCCATTTAATTATTGTTATATGTTTGGTTATCGTTTTCCCTCTA ACTTGCCCAAAGCTGGTTTTCTCCATTTAATTGTTGTTATATGTTTGGTTATCGTTTTCCCTCTA T C SLC38A2 Ensembl:ENSG00000134294 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1040925071 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1471916,Human_RBP_ID_1795387,Human_RBP_ID_2338470,Human_RBP_ID_3406140,Human_RBP_ID_5347241,Human_RBP_ID_6187256,Human_RBP_ID_17599740,Human_RBP_ID_22647356,Human_RBP_ID_24407133,Human_RBP_ID_24466353,Human_RBP_ID_24971925,Human_RBP_ID_26416087 RMVar_hsa_circ_96200,RMVar_hsa_circ_112311,RMVar_hsa_circ_156119,RMVar_hsa_circ_156120,RMVar_hsa_circ_3487,RMVar_hsa_circ_63504,RMVar_hsa_circ_61378,RMVar_hsa_circ_63530,RMVar_hsa_circ_354904,RMVar_hsa_circ_33645,RMVar_hsa_circ_305036 27422 RMVar_ID_27422 Human_SNP_ID_500023757 A-to-I Human chr12 + 47217250 47217250 47217250 TGATGAAACCCTGTCTCTAAAAAAAACTATAAAAATTAGCCAGGCATGGTGGCACAGGCCTGTAG TGATGAAACCCTGTCTCTAAAAAAAACTATAACAATTAGCCAGGCATGGTGGCACAGGCCTGTAG A C PCED1B Ensembl:ENSG00000179715 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs948883642 Functional Loss SNV dbSNP153 33..33 33 - - - 27423 RMVar_ID_27423 Human_SNP_ID_500024141 A-to-I Human chr12 + 47217702 47217702 47217702 AAGTTCAAGCAATTCTTGTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCACGCGACACCACT AAGTTCAAGCAATTCTTGTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCACGCGACACCACT A G PCED1B Ensembl:ENSG00000179715 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs970712960 Functional Loss SNV dbSNP153 33..33 33 - - - 27424 RMVar_ID_27424 Human_SNP_ID_500127144 A-to-I Human chr12 - 47614840 47614840 47614840 TGGAATTTATAACTAAAAGGGAAGGAGAAAGCAAATATTTGGAAAATTCTCAGCCTGGTCATGTA TGGAATTTATAACTAAAAGGGAAGGAGAAAGCCAATATTTGGAAAATTCTCAGCCTGGTCATGTA T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1340577329 Functional Loss SNV dbSNP153 33..33 33 - - - 27425 RMVar_ID_27425 Human_SNP_ID_500127170 A-to-I Human chr12 - 47615017 47615017 47615017 CATTGAACTTGGCTGAATTATGGTCATGTCCTAGAACTTTATGGAAGGCAGAACTTAAGAGTGAT CATTGAACTTGGCTGAATTATGGTCATGTCCTGGAACTTTATGGAAGGCAGAACTTAAGAGTGAT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991249295 Functional Loss SNV dbSNP153 33..33 33 - - - 27426 RMVar_ID_27426 Human_SNP_ID_500151288 A-to-I Human chr12 - 47704820 47704820 47704820 TTAGTAGAGATGGGGATCTCGAAGTGTTGCCCAGGCTGATCTAGGAACTCCTGAGCCCAAGCTAT TTAGTAGAGATGGGGATCTCGAAGTGTTGCCCGGGCTGATCTAGGAACTCCTGAGCCCAAGCTAT T C RPAP3 Ensembl:ENSG00000005175 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs930797388 Functional Loss SNV dbSNP153 33..33 33 - - - 27427 RMVar_ID_27427 Human_SNP_ID_500151306 A-to-I Human chr12 - 47704891 47704891 47704891 CTCCCACCTCAGCCTCCTGAGTAGCTGGAACTATAGGCACCCTCCACCACGCCTGGCTAATTTTT CTCCCACCTCAGCCTCCTGAGTAGCTGGAACTGTAGGCACCCTCCACCACGCCTGGCTAATTTTT T C RPAP3 Ensembl:ENSG00000005175 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1033494163 Functional Loss SNV dbSNP153 33..33 33 - - - 27428 RMVar_ID_27428 Human_SNP_ID_500177873 A-to-I Human chr12 - 47806589 47806589 47806589 CGCCTCCTGGGTTCAAGCGATTCTTGTGCCTCAGCCTCCCAAGTAGCTGGACTACATGCTCCCCG CGCCTCCTGGGTTCAAGCGATTCTTGTGCCTCGGCCTCCCAAGTAGCTGGACTACATGCTCCCCG T C HDAC7 Ensembl:ENSG00000061273 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs988574083 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_156148,RMVar_hsa_circ_121539 27429 RMVar_ID_27429 Human_SNP_ID_500186082 A-to-I Human chr12 - 47840268 47840268 47840268 GCTCTGTCACCCAGGCTGGAGTGCAGTGGCACAATCTCGGCTCACTGCAACCTCTGCCTCCCAGT GCTCTGTCACCCAGGCTGGAGTGCAGTGGCACGATCTCGGCTCACTGCAACCTCTGCCTCCCAGT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1254126310 Functional Loss SNV dbSNP153 33..33 33 - - - 27430 RMVar_ID_27430 Human_SNP_ID_500245194 A-to-I Human chr12 - 48074988 48074988 48074988 TGACTGGGCTGGTTTTGAACTTCTAGCCTCAAATGATCCTCCCCGCTTGTCCTCCCAAAGTGCTG TGACTGGGCTGGTTTTGAACTTCTAGCCTCAAGTGATCCTCCCCGCTTGTCCTCCCAAAGTGCTG T C SENP1 Ensembl:ENSG00000079387 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285550205 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7621,RMVar_hsa_circ_30087,RMVar_hsa_circ_301389,RMVar_hsa_circ_352520,RMVar_hsa_circ_53685,RMVar_hsa_circ_283609,RMVar_hsa_circ_156164,RMVar_hsa_circ_16080,RMVar_hsa_circ_156163,RMVar_hsa_circ_120714,RMVar_hsa_circ_156166,RMVar_hsa_circ_156165,RMVar_hsa_circ_308554,RMVar_hsa_circ_62168,RMVar_hsa_circ_366315,RMVar_hsa_circ_290786,RMVar_hsa_circ_156168,RMVar_hsa_circ_37478,RMVar_hsa_circ_118331,RMVar_hsa_circ_156170 27431 RMVar_ID_27431 Human_SNP_ID_500248531 A-to-I Human chr12 - 48088057 48088057 48088057 ACAGAGTGACCTCGTCTCAGAAAAAAAAAAAAAGATAGTCACAGAGAACTTTATGCTAGTTATTC ACAGAGTGACCTCGTCTCAGAAAAAAAAAAAAGGATAGTCACAGAGAACTTTATGCTAGTTATTC T C SENP1 Ensembl:ENSG00000079387 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1397029398 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25023458 RMVar_hsa_circ_30087,RMVar_hsa_circ_301389,RMVar_hsa_circ_352520,RMVar_hsa_circ_53685,RMVar_hsa_circ_283609,RMVar_hsa_circ_156164,RMVar_hsa_circ_16080,RMVar_hsa_circ_156163,RMVar_hsa_circ_120714,RMVar_hsa_circ_156166,RMVar_hsa_circ_156165,RMVar_hsa_circ_308554,RMVar_hsa_circ_62168,RMVar_hsa_circ_366315,RMVar_hsa_circ_290786,RMVar_hsa_circ_156168,RMVar_hsa_circ_37478,RMVar_hsa_circ_125042,RMVar_hsa_circ_118331,RMVar_hsa_circ_299846,RMVar_hsa_circ_361697,RMVar_hsa_circ_156170,RMVar_hsa_circ_319902,RMVar_hsa_circ_286150,RMVar_hsa_circ_156172,RMVar_hsa_circ_156174,RMVar_hsa_circ_12195,RMVar_hsa_circ_156173,RMVar_hsa_circ_156171 27432 RMVar_ID_27432 Human_SNP_ID_500260392 A-to-I Human chr12 + 48136028 48136028 48136028 CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCGCCTGGACCACGCCCGGCTAATATTTT CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTGCAGGCGCCTGGACCACGCCCGGCTAATATTTT A G PFKM Ensembl:ENSG00000152556 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1159543748 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6188758,Human_RBP_ID_11950143,Human_RBP_ID_17819864 RMVar_hsa_circ_60413,RMVar_hsa_circ_31436 27433 RMVar_ID_27433 Human_SNP_ID_500265307 A-to-I Human chr12 - 48155836 48155836 48155836 GGGAGGCTGAGGTTGCAGTGAGCTGAGATCGCACCACTGCACTCCAGCCTAGATGACAGAGTGAG GGGAGGCTGAGGTTGCAGTGAGCTGAGATCGCGCCACTGCACTCCAGCCTAGATGACAGAGTGAG T C ASB8 Ensembl:ENSG00000177981 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1162567251 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86553,RMVar_hsa_circ_156182 27434 RMVar_ID_27434 Human_SNP_ID_500310652 A-to-I Human chr12 - 48346828 48346796 48346828 TTTTGTGTTTTTAGTAGAGACAAGGTTTTGCCACGTTGGCCAGGCTGGTCTTGAACTGCTGACGT TTTTGTGTTTTTAGTAGAGACAAGGTTTTGCC________________________________T ACGTCAGCAGTTCAAGACCAGCCTGGCCAACGT A ZNF641 Ensembl:ENSG00000167528 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1353043994 Functional Loss DEL dbSNP153 33..64 33 - - - 27435 RMVar_ID_27435 Human_SNP_ID_500310662 A-to-I Human chr12 - 48346839 48346839 48346839 ACCTAGCTAATTTTTGTGTTTTTAGTAGAGACAAGGTTTTGCCACGTTGGCCAGGCTGGTCTTGA ACCTAGCTAATTTTTGTGTTTTTAGTAGAGACGAGGTTTTGCCACGTTGGCCAGGCTGGTCTTGA T C ZNF641 Ensembl:ENSG00000167528 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913658780 Functional Loss SNV dbSNP153 33..33 33 - - - 27436 RMVar_ID_27436 Human_SNP_ID_500310663 A-to-I Human chr12 - 48346839 48346839 48346839 ACCTAGCTAATTTTTGTGTTTTTAGTAGAGACAAGGTTTTGCCACGTTGGCCAGGCTGGTCTTGA ACCTAGCTAATTTTTGTGTTTTTAGTAGAGACCAGGTTTTGCCACGTTGGCCAGGCTGGTCTTGA T G ZNF641 Ensembl:ENSG00000167528 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913658780 Functional Loss SNV dbSNP153 33..33 33 - - - 27437 RMVar_ID_27437 Human_SNP_ID_500330559 A-to-I Human chr12 - 48426622 48426622 48426622 TTCAATGCTATTCTTATCAAACTACCAATGACATTTTTTATAGAACTAGAAACAACAATTTTAAA TTCAATGCTATTCTTATCAAACTACCAATGACGTTTTTTATAGAACTAGAAACAACAATTTTAAA T C lnc-BBS5-6 RNACentral:URS0000E2127A lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs751675207 Functional Loss SNV dbSNP153 33..33 33 - - - 27438 RMVar_ID_27438 Human_SNP_ID_500376733 A-to-I Human chr12 + 48604993 48604993 48604993 CTTCCACCTTAGCCTCCCAAGTAGCTGGGACTACGGGTGCACACCACCATGCCCAGCCAATTTTT CTTCCACCTTAGCCTCCCAAGTAGCTGGGACTGCGGGTGCACACCACCATGCCCAGCCAATTTTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs959952039 Functional Loss SNV dbSNP153 33..33 33 - - - 27439 RMVar_ID_27439 Human_SNP_ID_500389189 A-to-I Human chr12 - 48656493 48656493 48656493 CTGAGGTGGGCCAATCACTGGTCGGGAGATCAAGGCCATCCTGGCTAACATGGTGAAACCCTGTC CTGAGGTGGGCCAATCACTGGTCGGGAGATCAGGGCCATCCTGGCTAACATGGTGAAACCCTGTC T C KANSL2 Ensembl:ENSG00000139620 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs550138725 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79268,RMVar_hsa_circ_156186 27440 RMVar_ID_27440 Human_SNP_ID_500389426 A-to-I Human chr12 - 48657262 48657262 48657262 TGCCAAGACGCCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGC TGCCAAGACGCCTGGCTAATTTTTGTATTTTTGGTAGAGATGGGGTTTCACCATGTTGGCCAGGC T C KANSL2 Ensembl:ENSG00000139620 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs533491600 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24972835 RMVar_hsa_circ_79268,RMVar_hsa_circ_156186 27441 RMVar_ID_27441 Human_SNP_ID_500389452 A-to-I Human chr12 - 48657338 48657338 48657338 TCACTGCAACCTCTGCCTCCTGGGTTCAAGCAATTCTCCTGCCTCAGTGTCCTGAGTAGCTGGGA TCACTGCAACCTCTGCCTCCTGGGTTCAAGCAGTTCTCCTGCCTCAGTGTCCTGAGTAGCTGGGA T C KANSL2 Ensembl:ENSG00000139620 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs993445687 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79268,RMVar_hsa_circ_156186 27442 RMVar_ID_27442 Human_SNP_ID_500389453 A-to-I Human chr12 - 48657338 48657338 48657338 TCACTGCAACCTCTGCCTCCTGGGTTCAAGCAATTCTCCTGCCTCAGTGTCCTGAGTAGCTGGGA TCACTGCAACCTCTGCCTCCTGGGTTCAAGCACTTCTCCTGCCTCAGTGTCCTGAGTAGCTGGGA T G KANSL2 Ensembl:ENSG00000139620 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs993445687 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79268,RMVar_hsa_circ_156186 27443 RMVar_ID_27443 Human_SNP_ID_500389584 A-to-I Human chr12 - 48657810 48657810 48657810 GAGTTCTAGACTAGCCTGGCCAACATGGTGAAACTCCGTCTCTACCAAAAATACAACAATTAGCT GAGTTCTAGACTAGCCTGGCCAACATGGTGAAGCTCCGTCTCTACCAAAAATACAACAATTAGCT T C KANSL2 Ensembl:ENSG00000139620 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1056036509 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79268,RMVar_hsa_circ_156186 27444 RMVar_ID_27444 Human_SNP_ID_500389639 A-to-I Human chr12 - 48658014 48658014 48658014 GTTGGCCAGGCTGGTCTCAAGCTCCTGGCCTCAAGTGTTTCGCCCACCTTGGCCTCCCAAAGTGC GTTGGCCAGGCTGGTCTCAAGCTCCTGGCCTCGAGTGTTTCGCCCACCTTGGCCTCCCAAAGTGC T C KANSL2 Ensembl:ENSG00000139620 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs534392961 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79268,RMVar_hsa_circ_156186 27445 RMVar_ID_27445 Human_SNP_ID_500389640 A-to-I Human chr12 - 48658014 48658014 48658014 GTTGGCCAGGCTGGTCTCAAGCTCCTGGCCTCAAGTGTTTCGCCCACCTTGGCCTCCCAAAGTGC GTTGGCCAGGCTGGTCTCAAGCTCCTGGCCTCCAGTGTTTCGCCCACCTTGGCCTCCCAAAGTGC T G KANSL2 Ensembl:ENSG00000139620 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs534392961 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79268,RMVar_hsa_circ_156186 27446 RMVar_ID_27446 Human_SNP_ID_500389646 A-to-I Human chr12 - 48658059 48658059 48658059 GCTTGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTCAA GCTTGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGGTCTCAA T C KANSL2 Ensembl:ENSG00000139620 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1221151845 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79268,RMVar_hsa_circ_156186 27447 RMVar_ID_27447 Human_SNP_ID_500389653 A-to-I Human chr12 - 48658068 48658068 48658068 CCCCACTGTGCTTGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGC CCCCACTGTGCTTGGCTAATTTTTGTATTTTTTGTAGAGACAGGGTTTCACCATGTTGGCCAGGC T A KANSL2 Ensembl:ENSG00000139620 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1392523030 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79268,RMVar_hsa_circ_156186 27448 RMVar_ID_27448 Human_SNP_ID_500389670 A-to-I Human chr12 - 48658131 48658131 48658131 TGCCTCCTGGGTTCAAGCGATTCTCCGGTCTAAGCCTTCCGAGTAGTTGGGATTACAGGTGCGCC TGCCTCCTGGGTTCAAGCGATTCTCCGGTCTACGCCTTCCGAGTAGTTGGGATTACAGGTGCGCC T G KANSL2 Ensembl:ENSG00000139620 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs769628645 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79268,RMVar_hsa_circ_156186 27449 RMVar_ID_27449 Human_SNP_ID_500389776 A-to-I Human chr12 - 48658593 48658592 48658593 GCCACCATGTCTGGCTAATTTTTGTATTTTTTAGTAGAGATGGGGTTTCGCCATGTTGGCCAGGC GCCACCATGTCTGGCTAATTTTTGTATTTTTT_GTAGAGATGGGGTTTCGCCATGTTGGCCAGGC CT C KANSL2 Ensembl:ENSG00000139620 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1272932774 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_79268,RMVar_hsa_circ_156186 27450 RMVar_ID_27450 Human_SNP_ID_500389803 A-to-I Human chr12 - 48658694 48658694 48658694 GGAGTGCAGTGGCACGATCTCGGCTCACTGCAACCTTCACCATCTGGGTTCAAGCAATTCTCCTG GGAGTGCAGTGGCACGATCTCGGCTCACTGCAGCCTTCACCATCTGGGTTCAAGCAATTCTCCTG T C KANSL2 Ensembl:ENSG00000139620 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1164205631 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11951077 Human_Splice_Rec_1362429 RMVar_hsa_circ_79268,RMVar_hsa_circ_156186 27451 RMVar_ID_27451 Human_SNP_ID_500391195 A-to-I Human chr12 - 48664090 48664090 48664090 GCCAATATGGTGAAACCCCATCTCTACTAAATATACAAAAATTAGCCAGGCGTGGTGATGGGCAC GCCAATATGGTGAAACCCCATCTCTACTAAATTTACAAAAATTAGCCAGGCGTGGTGATGGGCAC T A KANSL2 Ensembl:ENSG00000139620 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1011992248 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117877,RMVar_hsa_circ_79268,RMVar_hsa_circ_156186,RMVar_hsa_circ_372714,RMVar_hsa_circ_371677,RMVar_hsa_circ_3561,RMVar_hsa_circ_156189,RMVar_hsa_circ_156191,RMVar_hsa_circ_110727,RMVar_hsa_circ_156190,RMVar_hsa_circ_293796,RMVar_hsa_circ_156188,RMVar_hsa_circ_274441,RMVar_hsa_circ_156193,RMVar_hsa_circ_156194 27452 RMVar_ID_27452 Human_SNP_ID_500391196 A-to-I Human chr12 - 48664090 48664090 48664090 GCCAATATGGTGAAACCCCATCTCTACTAAATATACAAAAATTAGCCAGGCGTGGTGATGGGCAC GCCAATATGGTGAAACCCCATCTCTACTAAATCTACAAAAATTAGCCAGGCGTGGTGATGGGCAC T G KANSL2 Ensembl:ENSG00000139620 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1011992248 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117877,RMVar_hsa_circ_79268,RMVar_hsa_circ_156186,RMVar_hsa_circ_372714,RMVar_hsa_circ_371677,RMVar_hsa_circ_3561,RMVar_hsa_circ_156189,RMVar_hsa_circ_156191,RMVar_hsa_circ_110727,RMVar_hsa_circ_156190,RMVar_hsa_circ_293796,RMVar_hsa_circ_156188,RMVar_hsa_circ_274441,RMVar_hsa_circ_156193,RMVar_hsa_circ_156194 27453 RMVar_ID_27453 Human_SNP_ID_500391632 A-to-I Human chr12 - 48665526 48665526 48665526 AGAATCTGACTCTGTCACCCAGGCTGGAGTGCAGTACCGTGATCTCAGCTTGCTGCATCCTCCAC AGAATCTGACTCTGTCACCCAGGCTGGAGTGCGGTACCGTGATCTCAGCTTGCTGCATCCTCCAC T C KANSL2 Ensembl:ENSG00000139620 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264891911 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11951283 RMVar_hsa_circ_117877,RMVar_hsa_circ_79268,RMVar_hsa_circ_156186,RMVar_hsa_circ_372714,RMVar_hsa_circ_371677,RMVar_hsa_circ_3561,RMVar_hsa_circ_156189,RMVar_hsa_circ_156191,RMVar_hsa_circ_110727,RMVar_hsa_circ_156190,RMVar_hsa_circ_293796,RMVar_hsa_circ_156188,RMVar_hsa_circ_274441,RMVar_hsa_circ_156193,RMVar_hsa_circ_156194 27454 RMVar_ID_27454 Human_SNP_ID_500391641 A-to-I Human chr12 - 48665555 48665555 48665555 TTATTTTCTTTATTTGTTTTTTTTGAGACAGAATCTGACTCTGTCACCCAGGCTGGAGTGCAGTA TTATTTTCTTTATTTGTTTTTTTTGAGACAGAGTCTGACTCTGTCACCCAGGCTGGAGTGCAGTA T C KANSL2 Ensembl:ENSG00000139620 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs75369053 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11951284 RMVar_hsa_circ_117877,RMVar_hsa_circ_79268,RMVar_hsa_circ_156186,RMVar_hsa_circ_372714,RMVar_hsa_circ_371677,RMVar_hsa_circ_3561,RMVar_hsa_circ_156189,RMVar_hsa_circ_156191,RMVar_hsa_circ_110727,RMVar_hsa_circ_156190,RMVar_hsa_circ_293796,RMVar_hsa_circ_156188,RMVar_hsa_circ_274441,RMVar_hsa_circ_156193,RMVar_hsa_circ_156194 27455 RMVar_ID_27455 Human_SNP_ID_500391783 A-to-I Human chr12 - 48666130 48666130 48666130 GATGGCTTACTGCCGTGATCTGCTGGGCTTAAACGATCTTCCCACCTCAGCCACCAGAGTAGCTG GATGGCTTACTGCCGTGATCTGCTGGGCTTAAGCGATCTTCCCACCTCAGCCACCAGAGTAGCTG T C KANSL2 Ensembl:ENSG00000139620 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1239540210 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6189235,Human_RBP_ID_11951316 RMVar_hsa_circ_117877,RMVar_hsa_circ_79268,RMVar_hsa_circ_156186,RMVar_hsa_circ_372714,RMVar_hsa_circ_371677,RMVar_hsa_circ_3561,RMVar_hsa_circ_156189,RMVar_hsa_circ_156191,RMVar_hsa_circ_110727,RMVar_hsa_circ_156190,RMVar_hsa_circ_293796,RMVar_hsa_circ_156188,RMVar_hsa_circ_274441,RMVar_hsa_circ_156193,RMVar_hsa_circ_156194 27456 RMVar_ID_27456 Human_SNP_ID_500391910 A-to-I Human chr12 - 48666530 48666530 48666530 TGCCACCACGCCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGT TGCCACCACGCCTGGCTAATTTTTGTATTTTTTGTAGAGATGGGGTTTCACCATGTTGGCCAGGT T A KANSL2 Ensembl:ENSG00000139620 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1401408040 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117877,RMVar_hsa_circ_79268,RMVar_hsa_circ_156186,RMVar_hsa_circ_372714,RMVar_hsa_circ_371677,RMVar_hsa_circ_3561,RMVar_hsa_circ_156189,RMVar_hsa_circ_156191,RMVar_hsa_circ_110727,RMVar_hsa_circ_156190,RMVar_hsa_circ_293796,RMVar_hsa_circ_156188,RMVar_hsa_circ_274441,RMVar_hsa_circ_156193,RMVar_hsa_circ_156194 27457 RMVar_ID_27457 Human_SNP_ID_500391977 A-to-I Human chr12 - 48666782 48666782 48666782 CAGCCTTAACTCCTGGGTCAAGCAATTCTCCTACCTCAGCCTTCTGAATAGCTGGGACTATGTAT CAGCCTTAACTCCTGGGTCAAGCAATTCTCCTGCCTCAGCCTTCTGAATAGCTGGGACTATGTAT T C KANSL2 Ensembl:ENSG00000139620 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs552318938 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117877,RMVar_hsa_circ_79268,RMVar_hsa_circ_156186,RMVar_hsa_circ_372714,RMVar_hsa_circ_371677,RMVar_hsa_circ_3561,RMVar_hsa_circ_156189,RMVar_hsa_circ_156191,RMVar_hsa_circ_110727,RMVar_hsa_circ_156190,RMVar_hsa_circ_293796,RMVar_hsa_circ_156188,RMVar_hsa_circ_274441,RMVar_hsa_circ_156193,RMVar_hsa_circ_156194 27458 RMVar_ID_27458 Human_SNP_ID_500391978 A-to-I Human chr12 - 48666782 48666782 48666782 CAGCCTTAACTCCTGGGTCAAGCAATTCTCCTACCTCAGCCTTCTGAATAGCTGGGACTATGTAT CAGCCTTAACTCCTGGGTCAAGCAATTCTCCTCCCTCAGCCTTCTGAATAGCTGGGACTATGTAT T G KANSL2 Ensembl:ENSG00000139620 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs552318938 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117877,RMVar_hsa_circ_79268,RMVar_hsa_circ_156186,RMVar_hsa_circ_372714,RMVar_hsa_circ_371677,RMVar_hsa_circ_3561,RMVar_hsa_circ_156189,RMVar_hsa_circ_156191,RMVar_hsa_circ_110727,RMVar_hsa_circ_156190,RMVar_hsa_circ_293796,RMVar_hsa_circ_156188,RMVar_hsa_circ_274441,RMVar_hsa_circ_156193,RMVar_hsa_circ_156194 27459 RMVar_ID_27459 Human_SNP_ID_500392027 A-to-I Human chr12 - 48666998 48666998 48666998 GTTTGTATTATTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAGCTCCTGACCT GTTTGTATTATTAGTAGAGATGGGGTTTCACCGTGTTGGCCAGGCTGGTCTCGAGCTCCTGACCT T C KANSL2 Ensembl:ENSG00000139620 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs915056420 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117877,RMVar_hsa_circ_79268,RMVar_hsa_circ_156186,RMVar_hsa_circ_372714,RMVar_hsa_circ_371677,RMVar_hsa_circ_3561,RMVar_hsa_circ_156189,RMVar_hsa_circ_156191,RMVar_hsa_circ_110727,RMVar_hsa_circ_156190,RMVar_hsa_circ_293796,RMVar_hsa_circ_156188,RMVar_hsa_circ_274441,RMVar_hsa_circ_156193,RMVar_hsa_circ_156194 27460 RMVar_ID_27460 Human_SNP_ID_500392065 A-to-I Human chr12 - 48667145 48667145 48667145 AGTTTTGCTCTAGTCTCCCAGGCTGGAGTGCAATGGCGTGATCTCGGCTCACTGCAACCTCCACC AGTTTTGCTCTAGTCTCCCAGGCTGGAGTGCAGTGGCGTGATCTCGGCTCACTGCAACCTCCACC T C KANSL2 Ensembl:ENSG00000139620 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs559732235 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12081985 RMVar_hsa_circ_117877,RMVar_hsa_circ_79268,RMVar_hsa_circ_156186,RMVar_hsa_circ_372714,RMVar_hsa_circ_371677,RMVar_hsa_circ_3561,RMVar_hsa_circ_156189,RMVar_hsa_circ_156191,RMVar_hsa_circ_110727,RMVar_hsa_circ_156190,RMVar_hsa_circ_293796,RMVar_hsa_circ_156188,RMVar_hsa_circ_274441,RMVar_hsa_circ_156193,RMVar_hsa_circ_156194 27461 RMVar_ID_27461 Human_SNP_ID_500394101 A-to-I Human chr12 - 48673726 48673726 48673726 CCAGGCTGGTCTTGAACTCCCAGGCTCAAGCAATCTGCCTGCCTCGGCCTCCCAAAGTGCTGGGA CCAGGCTGGTCTTGAACTCCCAGGCTCAAGCAGTCTGCCTGCCTCGGCCTCCCAAAGTGCTGGGA T C KANSL2 Ensembl:ENSG00000139620 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs142766130 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79268,RMVar_hsa_circ_156186,RMVar_hsa_circ_3561,RMVar_hsa_circ_110727,RMVar_hsa_circ_293796,RMVar_hsa_circ_156188,RMVar_hsa_circ_156194,RMVar_hsa_circ_327267,RMVar_hsa_circ_156197,RMVar_hsa_circ_156198,RMVar_hsa_circ_273268 27462 RMVar_ID_27462 Human_SNP_ID_500400326 A-to-I Human chr12 - 48696504 48696504 48696504 CTCAGGATAATAGGTAATAAATATTGACTTCTAGGCTTGAATACTGGCCCAGAAGTCAATGTTTT CTCAGGATAATAGGTAATAAATATTGACTTCTTGGCTTGAATACTGGCCCAGAAGTCAATGTTTT T A CCNT1 Ensembl:ENSG00000129315 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1325561774 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1166890,Human_RBP_ID_6189590,Human_RBP_ID_9017576,Human_RBP_ID_11952004 RMVar_hsa_circ_16284,RMVar_hsa_circ_95179,RMVar_hsa_circ_156201,RMVar_hsa_circ_49020,RMVar_hsa_circ_373149,RMVar_hsa_circ_156203 27463 RMVar_ID_27463 Human_SNP_ID_500400418 A-to-I Human chr12 - 48696918 48696918 48696918 TGAGGCACGAGAATTGCTTGAACCCAGGAGGCAGAGGGTGCTGTGAGCCGAGATTGCCCCACTGC TGAGGCACGAGAATTGCTTGAACCCAGGAGGCGGAGGGTGCTGTGAGCCGAGATTGCCCCACTGC T C CCNT1 Ensembl:ENSG00000129315 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1476224420 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16284,RMVar_hsa_circ_95179,RMVar_hsa_circ_156201,RMVar_hsa_circ_49020,RMVar_hsa_circ_373149,RMVar_hsa_circ_156203 27464 RMVar_ID_27464 Human_SNP_ID_500400432 A-to-I Human chr12 - 48696971 48696971 48696971 AAAATTGGCAGGGCAAGGTGGCACATGCATGTAGTACCAGCTACTCGGGAGGCTGAGGCACGAGA AAAATTGGCAGGGCAAGGTGGCACATGCATGTGGTACCAGCTACTCGGGAGGCTGAGGCACGAGA T C CCNT1 Ensembl:ENSG00000129315 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1433094360 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11952034 RMVar_hsa_circ_16284,RMVar_hsa_circ_95179,RMVar_hsa_circ_156201,RMVar_hsa_circ_49020,RMVar_hsa_circ_373149,RMVar_hsa_circ_156203 27465 RMVar_ID_27465 Human_SNP_ID_500400519 A-to-I Human chr12 - 48697317 48697317 48697317 TGGGGTTTCGCTATGTTGACTAGGCTGGTCTCAAACTCCTGGCCTCAAGTGATCCGCCTGCCTTG TGGGGTTTCGCTATGTTGACTAGGCTGGTCTCCAACTCCTGGCCTCAAGTGATCCGCCTGCCTTG T G CCNT1 Ensembl:ENSG00000129315 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1156889194 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16284,RMVar_hsa_circ_95179,RMVar_hsa_circ_156201,RMVar_hsa_circ_49020,RMVar_hsa_circ_373149,RMVar_hsa_circ_156203 27466 RMVar_ID_27466 Human_SNP_ID_500402228 A-to-I Human chr12 - 48703005 48703005 48703005 GTGATCATTTCACCTCAGCCTCCCAAGTTGCTAGGACTATAGCTGCGTGCCACCACTCCCAGTTA GTGATCATTTCACCTCAGCCTCCCAAGTTGCTGGGACTATAGCTGCGTGCCACCACTCCCAGTTA T C CCNT1 Ensembl:ENSG00000129315 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs375933564 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11952203 RMVar_hsa_circ_16284,RMVar_hsa_circ_6879,RMVar_hsa_circ_30204,RMVar_hsa_circ_156207,RMVar_hsa_circ_80875,RMVar_hsa_circ_156208 27467 RMVar_ID_27467 Human_SNP_ID_500423937 A-to-I Human chr12 - 48783859 48783859 48783859 AGGCTGGTCTTGAACTCCTGACCTTGTGATCTACCTGCCAGGGCCTTCCAAAGTGCTGGGATTAC AGGCTGGTCTTGAACTCCTGACCTTGTGATCTGCCTGCCAGGGCCTTCCAAAGTGCTGGGATTAC T C ADCY6 Ensembl:ENSG00000174233 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1259643537 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115446,RMVar_hsa_circ_78936,RMVar_hsa_circ_156219,RMVar_hsa_circ_156220 27468 RMVar_ID_27468 Human_SNP_ID_500423938 A-to-I Human chr12 - 48783859 48783859 48783859 AGGCTGGTCTTGAACTCCTGACCTTGTGATCTACCTGCCAGGGCCTTCCAAAGTGCTGGGATTAC AGGCTGGTCTTGAACTCCTGACCTTGTGATCTCCCTGCCAGGGCCTTCCAAAGTGCTGGGATTAC T G ADCY6 Ensembl:ENSG00000174233 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1259643537 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115446,RMVar_hsa_circ_78936,RMVar_hsa_circ_156219,RMVar_hsa_circ_156220 27469 RMVar_ID_27469 Human_SNP_ID_500438046 A-to-I Human chr12 - 48839040 48839040 48839040 TGAAAACCCATCTCTATAAAATTTTAAAAATTAGCCATCTGTGGTAGCATGCGCCTGTAGTCCCA TGAAAACCCATCTCTATAAAATTTTAAAAATTGGCCATCTGTGGTAGCATGCGCCTGTAGTCCCA T C DDX23 Ensembl:ENSG00000174243 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1049757923 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_156227,RMVar_hsa_circ_96672,RMVar_hsa_circ_60951 27470 RMVar_ID_27470 Human_SNP_ID_500438432 A-to-I Human chr12 - 48840408 48840408 48840408 TCTTAGCCTCCCAAAGTGCTGGGATTATAGGCATGAGACACCGCGCCTGGCCTAGGGGAAATATT TCTTAGCCTCCCAAAGTGCTGGGATTATAGGCGTGAGACACCGCGCCTGGCCTAGGGGAAATATT T C DDX23 Ensembl:ENSG00000174243 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1325060405 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_156227,RMVar_hsa_circ_96672,RMVar_hsa_circ_69018 27471 RMVar_ID_27471 Human_SNP_ID_500439916 A-to-I Human chr12 - 48844482 48844482 48844482 TTGAGGTGAGGAGTTTGAGAGCAGCCTGGCCAACATGGCAAAACCCCGTCTCTACTAAAAATACA TTGAGGTGAGGAGTTTGAGAGCAGCCTGGCCAGCATGGCAAAACCCCGTCTCTACTAAAAATACA T C DDX23 Ensembl:ENSG00000174243 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1402898290 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_156227,RMVar_hsa_circ_96672,RMVar_hsa_circ_69018,RMVar_hsa_circ_361039 27472 RMVar_ID_27472 Human_SNP_ID_500458887 A-to-I Human chr12 - 48919392 48919392 48919392 GGAGTTTGACCCAGCCTGGGCAACATGGCGAAACCCCATCTCTACAAAAAATACAAAAGTTAGCT GGAGTTTGACCCAGCCTGGGCAACATGGCGAAGCCCCATCTCTACAAAAAATACAAAAGTTAGCT T C AC073610.2 Ensembl:ENSG00000272822 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs888799411 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24973377 27473 RMVar_ID_27473 Human_SNP_ID_500458907 A-to-I Human chr12 - 48919487 48919487 48919487 AATTAATTAAAATGTAAGGGGGAGCTCAACGCAGTGGCTCATGCCTGTAATCCCAGCATTTTAGA AATTAATTAAAATGTAAGGGGGAGCTCAACGCTGTGGCTCATGCCTGTAATCCCAGCATTTTAGA T A AC073610.2 Ensembl:ENSG00000272822 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1208944319 Functional Loss SNV dbSNP153 33..33 33 - - - 27474 RMVar_ID_27474 Human_SNP_ID_500458964 A-to-I Human chr12 - 48919614 48919614 48919614 ACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAACTGGGGAGGTAAAGGTTGCAGCGAGCCAAGAT ACTCAGGAGGCTGAGGCAGGAGAATTGCTTGACCTGGGGAGGTAAAGGTTGCAGCGAGCCAAGAT T G AC073610.2 Ensembl:ENSG00000272822 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1282424503 Functional Loss SNV dbSNP153 33..33 33 - - - 27475 RMVar_ID_27475 Human_SNP_ID_500459015 A-to-I Human chr12 - 48919788 48919787 48919788 ATGTAGACCAGACGCGGTGGCTCACGCCTGTAATCCCAGCACTTGAGAAGCCAAAGTGGGTGGAT ATGTAGACCAGACGCGGTGGCTCACGCCTGTA_TCCCAGCACTTGAGAAGCCAAAGTGGGTGGAT AT A AC073610.2 Ensembl:ENSG00000272822 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs986025524 Functional Loss DEL dbSNP153 33..33 33 - - - 27476 RMVar_ID_27476 Human_SNP_ID_500461233 A-to-I Human chr12 - 48926650 48926650 48926650 TGTCTTTACTAAAAATTCAAAATCAGCTGGGCATGGTGGCGCATGCCTGTAGTCCCAGCTACTCG TGTCTTTACTAAAAATTCAAAATCAGCTGGGCGTGGTGGCGCATGCCTGTAGTCCCAGCTACTCG T C AC073610.2 Ensembl:ENSG00000272822 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1233810711 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17820134,Human_RBP_ID_27422102 27477 RMVar_ID_27477 Human_SNP_ID_500461314 A-to-I Human chr12 - 48926950 48926950 48926950 CAAAAATTAGCCAGGCGTGGTGGTGGGTGCCTATAATCCCAGCTACTCGGGAGGCTGAGAGAAAA CAAAAATTAGCCAGGCGTGGTGGTGGGTGCCTGTAATCCCAGCTACTCGGGAGGCTGAGAGAAAA T C AC073610.2 Ensembl:ENSG00000272822 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1229869947 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24973474 27478 RMVar_ID_27478 Human_SNP_ID_500461947 A-to-I Human chr12 - 48929398 48929398 48929398 TGTCACCTAGGCTGGAGTGCAGTGGCGTGATCATGGCTTACTGCAGCCTTGACCTCCTGGACGCA TGTCACCTAGGCTGGAGTGCAGTGGCGTGATCTTGGCTTACTGCAGCCTTGACCTCCTGGACGCA T A AC073610.2 Ensembl:ENSG00000272822 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs915075916 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24973525 27479 RMVar_ID_27479 Human_SNP_ID_500461958 A-to-I Human chr12 - 48929442 48929442 48929442 GAGGCTAGGGATCAGGGGCTTATTATTTTTTGAGACAAGGTCTCTGTCACCTAGGCTGGAGTGCA GAGGCTAGGGATCAGGGGCTTATTATTTTTTGCGACAAGGTCTCTGTCACCTAGGCTGGAGTGCA T G AC073610.2 Ensembl:ENSG00000272822 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 29129909,30559470 RNA-Seq:(High) rs1173916159 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6189888,Human_RBP_ID_9714003,Human_RBP_ID_17820142,Human_RBP_ID_18260805,Human_RBP_ID_22912203 27480 RMVar_ID_27480 Human_SNP_ID_500462292 A-to-I Human chr12 - 48930940 48930940 48930940 TAATTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGGGTCTCGATATCCTGACCTCGTG TAATTTTAGTAGAGACGGGGTTTCACCGTGTTGGCCAGGATGGGTCTCGATATCCTGACCTCGTG T C AC073610.2 Ensembl:ENSG00000272822 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1452591160 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24973537 27481 RMVar_ID_27481 Human_SNP_ID_500462301 A-to-I Human chr12 - 48930965 48930965 48930965 GCCACCACGCCTGGCTAATTTTTTGTAATTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGA GCCACCACGCCTGGCTAATTTTTTGTAATTTTGGTAGAGACGGGGTTTCACCGTGTTAGCCAGGA T C AC073610.2 Ensembl:ENSG00000272822 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs769325586 Functional Loss SNV dbSNP153 33..33 33 - - - 27482 RMVar_ID_27482 Human_SNP_ID_500462600 A-to-I Human chr12 - 48931955 48931955 48931955 CCTGTGGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGGATTGCTTGAGCCTGAGAGATTGAGGCT CCTGTGGTCCCAGCTACTCAGGAGGCTGAGGCTGGAGGATTGCTTGAGCCTGAGAGATTGAGGCT T A AC073610.2 Ensembl:ENSG00000272822 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 29129909,30559470 RNA-Seq:(High) rs757701030 Functional Loss SNV dbSNP153 33..33 33 - - - 27483 RMVar_ID_27483 Human_SNP_ID_500462601 A-to-I Human chr12 - 48931968 48931968 48931968 ATGGTGGCACGTGCCTGTGGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGGATTGCTTGAGCCTG ATGGTGGCACGTGCCTGTGGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGGATTGCTTGAGCCTG T C AC073610.2 Ensembl:ENSG00000272822 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1310761414 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24973549 27484 RMVar_ID_27484 Human_SNP_ID_500462618 A-to-I Human chr12 - 48932066 48932066 48932066 GCTCAAGCAGTCCTCCCACCCCAGCCTCCCAAAGTGCTGGATTTACAGGCATGAGCCATTGTGCC GCTCAAGCAGTCCTCCCACCCCAGCCTCCCAAGGTGCTGGATTTACAGGCATGAGCCATTGTGCC T C AC073610.2 Ensembl:ENSG00000272822 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1328164831 Functional Loss SNV dbSNP153 33..33 33 - - - 27485 RMVar_ID_27485 Human_SNP_ID_500463272 A-to-I Human chr12 - 48933539 48933539 48933539 TGCCACCATGCCCAGCTGATTTTTCTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGC TGCCACCATGCCCAGCTGATTTTTCTATTTTTGGTAGAGATGGGGTTTCACCATGTTGGCCAGGC T C AC073610.2 Ensembl:ENSG00000272822 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041544547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9687125 27486 RMVar_ID_27486 Human_SNP_ID_500463273 A-to-I Human chr12 - 48933539 48933539 48933539 TGCCACCATGCCCAGCTGATTTTTCTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGC TGCCACCATGCCCAGCTGATTTTTCTATTTTTCGTAGAGATGGGGTTTCACCATGTTGGCCAGGC T G AC073610.2 Ensembl:ENSG00000272822 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041544547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9687125 27487 RMVar_ID_27487 Human_SNP_ID_500463278 A-to-I Human chr12 - 48933580 48933580 48933580 TCTCCTGCCTCAGCCTCCGAGTAGCTGGGACTACAGGTATGTGCCACCATGCCCAGCTGATTTTT TCTCCTGCCTCAGCCTCCGAGTAGCTGGGACTGCAGGTATGTGCCACCATGCCCAGCTGATTTTT T C AC073610.2 Ensembl:ENSG00000272822 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1208923885 Functional Loss SNV dbSNP153 33..33 33 - - - 27488 RMVar_ID_27488 Human_SNP_ID_500463561 A-to-I Human chr12 - 48934847 48934847 48934847 CCACCACACCCGGCTAATTTTGTATTTTTAGTAGAGATGGGTTTCTCCATGTTAGTGAGACTGGT CCACCACACCCGGCTAATTTTGTATTTTTAGTGGAGATGGGTTTCTCCATGTTAGTGAGACTGGT T C AC073610.2 Ensembl:ENSG00000272822 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs762493028 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11953294 27489 RMVar_ID_27489 Human_SNP_ID_500463599 A-to-I Human chr12 - 48934972 48934972 48934972 TCTTGTTGCCCAGGCTGGAGGGCAATGGCACGATATCGGCTCACCACAGCCTCTCCTCCTGGGCT TCTTGTTGCCCAGGCTGGAGGGCAATGGCACGGTATCGGCTCACCACAGCCTCTCCTCCTGGGCT T C AC073610.2 Ensembl:ENSG00000272822 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1180749868 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11953296,Human_RBP_ID_22904395 27490 RMVar_ID_27490 Human_SNP_ID_500463604 A-to-I Human chr12 - 48934980 48934980 48934980 GAATTTGGTCTTGTTGCCCAGGCTGGAGGGCAATGGCACGATATCGGCTCACCACAGCCTCTCCT GAATTTGGTCTTGTTGCCCAGGCTGGAGGGCAGTGGCACGATATCGGCTCACCACAGCCTCTCCT T C AC073610.2 Ensembl:ENSG00000272822 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1323394153 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11953296,Human_RBP_ID_19828137,Human_RBP_ID_23561467 27491 RMVar_ID_27491 Human_SNP_ID_500464293 A-to-I Human chr12 - 48937705 48937705 48937705 GCTGACCTTAGTATCAACCCCCCTCTTCTCCAACTCTTGTTTTCTAGTCCAGGATATGCTAAAGG GCTGACCTTAGTATCAACCCCCCTCTTCTCCAGCTCTTGTTTTCTAGTCCAGGATATGCTAAAGG T C ARF3,AC073610.2 Ensembl:ENSG00000134287,Ensembl:ENSG00000272822 Protein coding,Protein coding 3'UTR,intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs551841915 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_992470,Human_RBP_ID_11953465,Human_RBP_ID_17471515,Human_RBP_ID_17820209,Human_RBP_ID_19773910,Human_RBP_ID_23561553,Human_RBP_ID_26906768 Human_miRNA_ID_1161788,Human_miRNA_ID_2542033,Human_miRNA_ID_2545753,Human_miRNA_ID_2556751,Human_miRNA_ID_2558634,Human_miRNA_ID_2589052 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 27492 RMVar_ID_27492 Human_SNP_ID_500501256 A-to-I Human chr12 - 49068551 49068550 49068551 CACGCCTGTAATCCCAGCTACAAAGGAGACTGAGGTAGGAGAATCGCTTGAACCCAGGAGGCAAA CACGCCTGTAATCCCAGCTACAAAGGAGACTG_GGTAGGAGAATCGCTTGAACCCAGGAGGCAAA CT C RHEBL1 Ensembl:ENSG00000167550 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1023036600 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_127854,RMVar_hsa_circ_156283 27493 RMVar_ID_27493 Human_SNP_ID_500511177 A-to-I Human chr12 - 49106222 49106222 49106222 TAATAGTTTGAGCATATAAAGAGGAACTTGTGATGGGAGAGATCTAGGGAGGAGTAAAGAAGTAT TAATAGTTTGAGCATATAAAGAGGAACTTGTGGTGGGAGAGATCTAGGGAGGAGTAAAGAAGTAT T C LMBR1L Ensembl:ENSG00000139636 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs746967562 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28682,RMVar_hsa_circ_96022,RMVar_hsa_circ_156288,RMVar_hsa_circ_299915,RMVar_hsa_circ_156291,RMVar_hsa_circ_156293,RMVar_hsa_circ_3959,RMVar_hsa_circ_364739,RMVar_hsa_circ_156294,RMVar_hsa_circ_374989 27494 RMVar_ID_27494 Human_SNP_ID_500519727 A-to-I Human chr12 + 49135654 49135654 49135654 CAGGCATGTGCCACGACACCTGGCTATTTTTTATATTTTTAGCAGAGAGGGGGTTTTGCCGTGTT CAGGCATGTGCCACGACACCTGGCTATTTTTTGTATTTTTAGCAGAGAGGGGGTTTTGCCGTGTT A G AC011603.3 Ensembl:ENSG00000258017 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560437886 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5246399 27495 RMVar_ID_27495 Human_SNP_ID_500521261 A-to-I Human chr12 + 49141153 49141153 49141153 GGGAGACAGTGGTTGCAGTGACCTGAGATCGCACCACTGCACTCCAGCCTGGGCGGCTAAGCGAG GGGAGACAGTGGTTGCAGTGACCTGAGATCGCTCCACTGCACTCCAGCCTGGGCGGCTAAGCGAG A T AC011603.3 Ensembl:ENSG00000258017 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1194917620 Functional Loss SNV dbSNP153 33..33 33 - - - 27496 RMVar_ID_27496 Human_SNP_ID_500521514 A-to-I Human chr12 + 49142201 49142201 49142201 GCGATCCTCTCACCTCAGCCTCCTGAGTAGCTAGGACCACAAGTGTATGCCACCACACCCTGCTA GCGATCCTCTCACCTCAGCCTCCTGAGTAGCTGGGACCACAAGTGTATGCCACCACACCCTGCTA A G AC011603.3 Ensembl:ENSG00000258017 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909133385 Functional Loss SNV dbSNP153 33..33 33 - - - 27497 RMVar_ID_27497 Human_SNP_ID_500527366 A-to-I Human chr12 + 49164127 49164126 49164127 CTGACCTTATGATCCCCCTGCCACAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCACG CTGACCTTATGATCCCCCTGCCACAGCCTCCC_AAGTGCTGGGATTACAGGCGTGAGCCACCACG CA C AC011603.3 Ensembl:ENSG00000258017 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031894515 Functional Loss DEL dbSNP153 33..33 33 - - - 27498 RMVar_ID_27498 Human_SNP_ID_500527587 A-to-I Human chr12 + 49165207 49165207 49165207 ACAACATGCTTCTTTTGGGGGACGGGGGAGATAGGGTCTTGCTCTGTTGCCCAGGCTTAAGTGCA ACAACATGCTTCTTTTGGGGGACGGGGGAGATGGGGTCTTGCTCTGTTGCCCAGGCTTAAGTGCA A G AC011603.3 Ensembl:ENSG00000258017 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928153349 Functional Loss SNV dbSNP153 33..33 33 - - - 27499 RMVar_ID_27499 Human_SNP_ID_500550683 A-to-I Human chr12 - 49261000 49261000 49261000 GCCAGGTGAGGTGGCTCATTTCTGTAATCTCAACACTTTGGGAGGCCAGGGTGGGCAGATTGCTT GCCAGGTGAGGTGGCTCATTTCTGTAATCTCAGCACTTTGGGAGGCCAGGGTGGGCAGATTGCTT T C AC010173.1 Ensembl:ENSG00000258101 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1228770767 Functional Loss SNV dbSNP153 33..33 33 - - - 27500 RMVar_ID_27500 Human_SNP_ID_500552607 A-to-I Human chr12 + 49267538 49267538 49267538 AAAATAAGGCAGGCATGGTGGTGGGCACCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAAA AAAATAAGGCAGGCATGGTGGTGGGCACCTGTGATCCCAGCTACTTGGGAGGCTGAGGCAGGAAA A G TUBA1C Ensembl:ENSG00000167553 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs538744990 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118502,RMVar_hsa_circ_48699,RMVar_hsa_circ_96118,RMVar_hsa_circ_156314,RMVar_hsa_circ_156315 27501 RMVar_ID_27501 Human_SNP_ID_500552894 A-to-I Human chr12 + 49268425 49268424 49268426 TCTACCATAATTTTTTTTTTTTTTGTATTTTTAATAGAGACAGTTTCACCATGTTGGCCAGGCTG TCTACCATAATTTTTTTTTTTTTTGTATTTTT__TAGAGACAGTTTCACCATGTTGGCCAGGCTG TAA T TUBA1C Ensembl:ENSG00000167553 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1368123038 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_11954920 RMVar_hsa_circ_118502,RMVar_hsa_circ_48699,RMVar_hsa_circ_96118,RMVar_hsa_circ_156314,RMVar_hsa_circ_156315 27502 RMVar_ID_27502 Human_SNP_ID_500552895 A-to-I Human chr12 + 49268425 49268425 49268425 TCTACCATAATTTTTTTTTTTTTTGTATTTTTAATAGAGACAGTTTCACCATGTTGGCCAGGCTG TCTACCATAATTTTTTTTTTTTTTGTATTTTTTATAGAGACAGTTTCACCATGTTGGCCAGGCTG A T TUBA1C Ensembl:ENSG00000167553 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1472937144 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11954920 RMVar_hsa_circ_118502,RMVar_hsa_circ_48699,RMVar_hsa_circ_96118,RMVar_hsa_circ_156314,RMVar_hsa_circ_156315 27503 RMVar_ID_27503 Human_SNP_ID_500552898 A-to-I Human chr12 + 49268428 49268427 49268429 ACCATAATTTTTTTTTTTTTTGTATTTTTAATAGAGACAGTTTCACCATGTTGGCCAGGCTGATT ACCATAATTTTTTTTTTTTTTGTATTTTTAAT__AGACAGTTTCACCATGTTGGCCAGGCTGATT TAG T TUBA1C Ensembl:ENSG00000167553 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1284776487 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_11954920 RMVar_hsa_circ_118502,RMVar_hsa_circ_48699,RMVar_hsa_circ_96118,RMVar_hsa_circ_156314,RMVar_hsa_circ_156315 27504 RMVar_ID_27504 Human_SNP_ID_500553081 A-to-I Human chr12 + 49269199 49269199 49269199 CTCCTCCCTCAGCCTCCCAAGTAGCTGGGACTACAGGTGTGCGCCATCATGCCTGGCTAATTTTT CTCCTCCCTCAGCCTCCCAAGTAGCTGGGACTGCAGGTGTGCGCCATCATGCCTGGCTAATTTTT A G TUBA1C Ensembl:ENSG00000167553 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs980355030 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118502,RMVar_hsa_circ_48699,RMVar_hsa_circ_96118,RMVar_hsa_circ_156314,RMVar_hsa_circ_156315 27505 RMVar_ID_27505 Human_SNP_ID_500553324 A-to-I Human chr12 - 49269876 49269871 49269876 AGTTATTGGCAGCATCTTCCTTGCCTGTGATGAGTTGCTCAGGGTGGAAGAGCTGGCGGTAAGTG AGTTATTGGCAGCATCTTCCTTGCCTGTGATG_____CTCAGGGTGGAAGAGCTGGCGGTAAGTG GCAACT G AC125611.3 Ensembl:ENSG00000258232 lincRNA intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1315056556 Functional Loss DEL dbSNP153 33..37 33 - - - 27506 RMVar_ID_27506 Human_SNP_ID_500554128 A-to-I Human chr12 + 49272831 49272831 49272831 CGCCATGGTAAATACATGGCTTGCTGCCTGTTATACCGTGGTGACGTGGTTCCCAAAGATGTCAA CGCCATGGTAAATACATGGCTTGCTGCCTGTTGTACCGTGGTGACGTGGTTCCCAAAGATGTCAA A G TUBA1C Ensembl:ENSG00000167553 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs538625739 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_420863,Human_RBP_ID_992579,Human_RBP_ID_1166986,Human_RBP_ID_1357667,Human_RBP_ID_1472650,Human_RBP_ID_1796057,Human_RBP_ID_2339963,Human_RBP_ID_4225275,Human_RBP_ID_6190726,Human_RBP_ID_8377171,Human_RBP_ID_8782349,Human_RBP_ID_9017686,Human_RBP_ID_9255238,Human_RBP_ID_9278088,Human_RBP_ID_17650641,Human_RBP_ID_17668954,Human_RBP_ID_22037822,Human_RBP_ID_22174390,Human_RBP_ID_22435842,Human_RBP_ID_22755892,Human_RBP_ID_23125600,Human_RBP_ID_23561892,Human_RBP_ID_26768247,Human_RBP_ID_26907130,Human_RBP_ID_27214942,Human_RBP_ID_27629915 Human_miRNA_ID_497410,Human_miRNA_ID_2171892 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 27507 RMVar_ID_27507 Human_SNP_ID_500554140 A-to-I Human chr12 + 49272884 49272884 49272884 CAAAGATGTCAATGCTGCCATTGCCACCATCAAAACCAAGCGTACCATCCAGTTTGTGGATTGGT CAAAGATGTCAATGCTGCCATTGCCACCATCACAACCAAGCGTACCATCCAGTTTGTGGATTGGT A C TUBA1C Ensembl:ENSG00000167553 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1266935758 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2339965,Human_RBP_ID_5139602,Human_RBP_ID_8377173,Human_RBP_ID_22755893,Human_RBP_ID_26612835 Human_miRNA_ID_88037,Human_miRNA_ID_1957197 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 27508 RMVar_ID_27508 Human_SNP_ID_500554144 A-to-I Human chr12 - 49272894 49272894 49272894 CCAGTGGGGCACCAATCCACAAACTGGATGGTACGCTTGGTTTTGATGGTGGCAATGGCAGCATT CCAGTGGGGCACCAATCCACAAACTGGATGGTGCGCTTGGTTTTGATGGTGGCAATGGCAGCATT T C AC125611.3 Ensembl:ENSG00000258232 lincRNA exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs537291300 Functional Loss SNV dbSNP153 33..33 33 - - - 27509 RMVar_ID_27509 Human_SNP_ID_500554153 A-to-I Human chr12 - 49272942 49272939 49272943 CCGCCAGGCACCACAGTGGGAGGCTGGTAATTAATGCCAACCTTGAAGCCAGTGGGGCACCAATC CCGCCAGGCACCACAGTGGGAGGCTGGTAAT____GCCAACCTTGAAGCCAGTGGGGCACCAATC CATTA C AC125611.3 Ensembl:ENSG00000258232 lincRNA exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs759403410 Functional Loss DEL dbSNP153 32..35 33 - - - 27510 RMVar_ID_27510 Human_SNP_ID_500554154 A-to-I Human chr12 - 49272942 49272942 49272942 CCGCCAGGCACCACAGTGGGAGGCTGGTAATTAATGCCAACCTTGAAGCCAGTGGGGCACCAATC CCGCCAGGCACCACAGTGGGAGGCTGGTAATTGATGCCAACCTTGAAGCCAGTGGGGCACCAATC T C AC125611.3 Ensembl:ENSG00000258232 lincRNA exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs771134260 Functional Loss SNV dbSNP153 33..33 33 - - - 27511 RMVar_ID_27511 Human_SNP_ID_500554176 A-to-I Human chr12 - 49273026 49273026 49273026 TTGTGGTCCAGGCGAGCCCAGGCCTCGGCAACAGCTGTGGTATTGCTCAGCATGCACACAGCTCT TTGTGGTCCAGGCGAGCCCAGGCCTCGGCAACTGCTGTGGTATTGCTCAGCATGCACACAGCTCT T A AC125611.3 Ensembl:ENSG00000258232 lincRNA exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs779858377 Functional Loss SNV dbSNP153 33..33 33 - - - 27512 RMVar_ID_27512 Human_SNP_ID_500554177 A-to-I Human chr12 - 49273026 49273026 49273026 TTGTGGTCCAGGCGAGCCCAGGCCTCGGCAACAGCTGTGGTATTGCTCAGCATGCACACAGCTCT TTGTGGTCCAGGCGAGCCCAGGCCTCGGCAACGGCTGTGGTATTGCTCAGCATGCACACAGCTCT T C AC125611.3 Ensembl:ENSG00000258232 lincRNA exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs779858377 Functional Loss SNV dbSNP153 33..33 33 - - - 27513 RMVar_ID_27513 Human_SNP_ID_500568185 A-to-I Human chr12 + 49324601 49324601 49324601 TGTCTTATGTAACATTCTATGAACATTTGGTGACCAGGTGTGGTGGCTCACGCCTGTAATTCCAA TGTCTTATGTAACATTCTATGAACATTTGGTGGCCAGGTGTGGTGGCTCACGCCTGTAATTCCAA A G TROAP Ensembl:ENSG00000135451 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs535800817 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8377222,Human_RBP_ID_11955075 RMVar_hsa_circ_21287 27514 RMVar_ID_27514 Human_SNP_ID_500568362 A-to-I Human chr12 + 49325116 49325116 49325116 TTTGTTTTTGTTTTTTGTAGAGATGGGGTTTTACCATGTTGGCCAGGCTGGTCTCAAACTCCTGA TTTGTTTTTGTTTTTTGTAGAGATGGGGTTTTGCCATGTTGGCCAGGCTGGTCTCAAACTCCTGA A G TROAP Ensembl:ENSG00000135451 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1197698050 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11955105 RMVar_hsa_circ_21287 27515 RMVar_ID_27515 Human_SNP_ID_500568391 A-to-I Human chr12 + 49325256 49325256 49325256 TTGTATTTTTTTAGTGGAGACAGGGTTTTGCTATGTTGGCCGGGTTGGTCTCAAACTCCTGACCA TTGTATTTTTTTAGTGGAGACAGGGTTTTGCTCTGTTGGCCGGGTTGGTCTCAAACTCCTGACCA A C TROAP Ensembl:ENSG00000135451 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1013663248 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21287 27516 RMVar_ID_27516 Human_SNP_ID_500568392 A-to-I Human chr12 + 49325256 49325256 49325256 TTGTATTTTTTTAGTGGAGACAGGGTTTTGCTATGTTGGCCGGGTTGGTCTCAAACTCCTGACCA TTGTATTTTTTTAGTGGAGACAGGGTTTTGCTGTGTTGGCCGGGTTGGTCTCAAACTCCTGACCA A G TROAP Ensembl:ENSG00000135451 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1013663248 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21287 27517 RMVar_ID_27517 Human_SNP_ID_500568409 A-to-I Human chr12 + 49325336 49325336 49325336 CCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGCACCCAGCCATCTATTTCTTAA CCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCACCCAGCCATCTATTTCTTAA A G TROAP Ensembl:ENSG00000135451 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1352332134 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21287 27518 RMVar_ID_27518 Human_SNP_ID_500576513 A-to-I Human chr12 + 49353375 49353375 49353375 ATATCATTTTTAAAGTGGAATTATGACCAGGCATGGTGCCTCTTGCCTATAATCCTAGCACTTTG ATATCATTTTTAAAGTGGAATTATGACCAGGCGTGGTGCCTCTTGCCTATAATCCTAGCACTTTG A G DNAJC22 Ensembl:ENSG00000178401 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs937520303 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_420946 27519 RMVar_ID_27519 Human_SNP_ID_500576516 A-to-I Human chr12 + 49353391 49353389 49353391 GGAATTATGACCAGGCATGGTGCCTCTTGCCTATAATCCTAGCACTTTGGCAAGCCAAGGCAGGA GGAATTATGACCAGGCATGGTGCCTCTTGCC__TAATCCTAGCACTTTGGCAAGCCAAGGCAGGA CTA C DNAJC22 Ensembl:ENSG00000178401 Protein coding 3'UTR GSE100210;GSE99789;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,29796672,31158229,31158229 RNA-Seq:(High) rs1296138481 Functional Loss DEL dbSNP153 32..33 33 - - - 27520 RMVar_ID_27520 Human_SNP_ID_500576517 A-to-I Human chr12 + 49353393 49353390 49353394 AATTATGACCAGGCATGGTGCCTCTTGCCTATAATCCTAGCACTTTGGCAAGCCAAGGCAGGAAG AATTATGACCAGGCATGGTGCCTCTTGCCT____TCCTAGCACTTTGGCAAGCCAAGGCAGGAAG TATAA T DNAJC22 Ensembl:ENSG00000178401 Protein coding 3'UTR GSE100210;GSE99789;GSE99789;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,29796672,29796672,31158229,31158229,31158229 RNA-Seq:(High) rs1207982260 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_11955220 27521 RMVar_ID_27521 Human_SNP_ID_500576518 A-to-I Human chr12 + 49353391 49353391 49353391 GGAATTATGACCAGGCATGGTGCCTCTTGCCTATAATCCTAGCACTTTGGCAAGCCAAGGCAGGA GGAATTATGACCAGGCATGGTGCCTCTTGCCTGTAATCCTAGCACTTTGGCAAGCCAAGGCAGGA A G DNAJC22 Ensembl:ENSG00000178401 Protein coding 3'UTR GSE100210;GSE99789;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,29796672,31158229,31158229 RNA-Seq:(High) rs1135757 Functional Loss SNV dbSNP153 33..33 33 - - - 27522 RMVar_ID_27522 Human_SNP_ID_500576559 A-to-I Human chr12 + 49353572 49353572 49353572 GGAGGCTGAGATTGGGAGGATCACTTGAACCCAAAAGGTGGAGGCTGCAGTGAGCTGAGATCGTA GGAGGCTGAGATTGGGAGGATCACTTGAACCCGAAAGGTGGAGGCTGCAGTGAGCTGAGATCGTA A G DNAJC22 Ensembl:ENSG00000178401 Protein coding 3'UTR GSE100210;GSE99789;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BERP35T4 cell line - 29129909,29796672,31158229 RNA-Seq:(High) rs1240060945 Functional Loss SNV dbSNP153 33..33 33 - - - 27523 RMVar_ID_27523 Human_SNP_ID_500581451 A-to-I Human chr12 + 49374027 49374027 49374027 AGGATTGCTTGAGCCCAAGAGTTTGAGATTGTAGTGAGCTATGATCATGTCACTGCACTCCAACC AGGATTGCTTGAGCCCAAGAGTTTGAGATTGTCGTGAGCTATGATCATGTCACTGCACTCCAACC A C SPATS2 Ensembl:ENSG00000123352 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs748359290 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67313,RMVar_hsa_circ_110999,RMVar_hsa_circ_363495,RMVar_hsa_circ_108787,RMVar_hsa_circ_156328,RMVar_hsa_circ_156329,RMVar_hsa_circ_156327 27524 RMVar_ID_27524 Human_SNP_ID_500581483 A-to-I Human chr12 + 49374150 49374150 49374150 TGTTATTATTTTTTAATTTTTATTTTTTTTGGAAACAGGGTTTTGCTCTGTCACCCAGGCTGGAG TGTTATTATTTTTTAATTTTTATTTTTTTTGGTAACAGGGTTTTGCTCTGTCACCCAGGCTGGAG A T SPATS2 Ensembl:ENSG00000123352 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1250188919 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11955356 RMVar_hsa_circ_67313,RMVar_hsa_circ_110999,RMVar_hsa_circ_363495,RMVar_hsa_circ_108787,RMVar_hsa_circ_156328,RMVar_hsa_circ_156329,RMVar_hsa_circ_156327 27525 RMVar_ID_27525 Human_SNP_ID_500581509 A-to-I Human chr12 + 49374262 49374262 49374262 CAGGTGATTCTGTCACCTCAGCCTCAGTAGCTAGGACTGCAGGCACACACCATGGCAGTCAGCTA CAGGTGATTCTGTCACCTCAGCCTCAGTAGCTCGGACTGCAGGCACACACCATGGCAGTCAGCTA A C SPATS2 Ensembl:ENSG00000123352 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs575273153 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17561092 RMVar_hsa_circ_67313,RMVar_hsa_circ_110999,RMVar_hsa_circ_363495,RMVar_hsa_circ_108787,RMVar_hsa_circ_156328,RMVar_hsa_circ_156329,RMVar_hsa_circ_156327 27526 RMVar_ID_27526 Human_SNP_ID_500581510 A-to-I Human chr12 + 49374262 49374262 49374262 CAGGTGATTCTGTCACCTCAGCCTCAGTAGCTAGGACTGCAGGCACACACCATGGCAGTCAGCTA CAGGTGATTCTGTCACCTCAGCCTCAGTAGCTGGGACTGCAGGCACACACCATGGCAGTCAGCTA A G SPATS2 Ensembl:ENSG00000123352 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs575273153 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17561092 RMVar_hsa_circ_67313,RMVar_hsa_circ_110999,RMVar_hsa_circ_363495,RMVar_hsa_circ_108787,RMVar_hsa_circ_156328,RMVar_hsa_circ_156329,RMVar_hsa_circ_156327 27527 RMVar_ID_27527 Human_SNP_ID_500581525 A-to-I Human chr12 + 49374312 49374312 49374312 CATGGCAGTCAGCTAGTTTTAAAATTTTTTGTAGAGACAGGGTCTTGCTTTGTTGCCCAGGCTGG CATGGCAGTCAGCTAGTTTTAAAATTTTTTGTGGAGACAGGGTCTTGCTTTGTTGCCCAGGCTGG A G SPATS2 Ensembl:ENSG00000123352 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1347303046 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67313,RMVar_hsa_circ_110999,RMVar_hsa_circ_363495,RMVar_hsa_circ_108787,RMVar_hsa_circ_156328,RMVar_hsa_circ_156329,RMVar_hsa_circ_156327 27528 RMVar_ID_27528 Human_SNP_ID_500582503 A-to-I Human chr12 + 49378059 49378059 49378059 CAATGGCACGATCTTGGCTCACTGCCACCTCCAGCTCCAGGGTTCAAGCGATTCCCCTGCCTCAG CAATGGCACGATCTTGGCTCACTGCCACCTCCGGCTCCAGGGTTCAAGCGATTCCCCTGCCTCAG A G SPATS2 Ensembl:ENSG00000123352 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1394790475 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67313,RMVar_hsa_circ_110999,RMVar_hsa_circ_363495,RMVar_hsa_circ_108787,RMVar_hsa_circ_156328,RMVar_hsa_circ_156329,RMVar_hsa_circ_156327 27529 RMVar_ID_27529 Human_SNP_ID_500584910 A-to-I Human chr12 + 49387578 49387578 49387578 AGAATCTCTTGAAGCTGGGAGGTTGAGGTTGCAGTGAGCTGAGATCACGCCACTGCACACTCCAG AGAATCTCTTGAAGCTGGGAGGTTGAGGTTGCGGTGAGCTGAGATCACGCCACTGCACACTCCAG A G SPATS2 Ensembl:ENSG00000123352 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1305167073 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24974415 RMVar_hsa_circ_67313,RMVar_hsa_circ_110999,RMVar_hsa_circ_108787,RMVar_hsa_circ_78709,RMVar_hsa_circ_156328,RMVar_hsa_circ_156327,RMVar_hsa_circ_156330 27530 RMVar_ID_27530 Human_SNP_ID_500585220 A-to-I Human chr12 + 49388824 49388824 49388824 TCAAGTGATCCTCCCTCTTCAGCCTCATAAGTAGCTGGTACTGTAGGCACAAGTCCCCATGCCCA TCAAGTGATCCTCCCTCTTCAGCCTCATAAGTGGCTGGTACTGTAGGCACAAGTCCCCATGCCCA A G SPATS2 Ensembl:ENSG00000123352 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1483547296 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11955654 RMVar_hsa_circ_67313,RMVar_hsa_circ_110999,RMVar_hsa_circ_108787,RMVar_hsa_circ_78709,RMVar_hsa_circ_156328,RMVar_hsa_circ_156327,RMVar_hsa_circ_156330 27531 RMVar_ID_27531 Human_SNP_ID_500586575 A-to-I Human chr12 + 49394979 49394979 49394979 CCTGTAATCCCAGCTACTCAGGAGACTGAGGCAGGAGAATCCCTTGAACCCAGGAGGCGGAGGTT CCTGTAATCCCAGCTACTCAGGAGACTGAGGCCGGAGAATCCCTTGAACCCAGGAGGCGGAGGTT A C SPATS2 Ensembl:ENSG00000123352 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251995312 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67313,RMVar_hsa_circ_110999,RMVar_hsa_circ_108787,RMVar_hsa_circ_78709,RMVar_hsa_circ_156328,RMVar_hsa_circ_156327,RMVar_hsa_circ_156330 27532 RMVar_ID_27532 Human_SNP_ID_500586741 A-to-I Human chr12 + 49395655 49395655 49395655 ACCATGTTGATTAGGCTGGTCTTGAACTCCTGACCGCAGGTGATCCACCCGCCTCAGCCTCCCAA ACCATGTTGATTAGGCTGGTCTTGAACTCCTGGCCGCAGGTGATCCACCCGCCTCAGCCTCCCAA A G SPATS2 Ensembl:ENSG00000123352 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1165062281 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67313,RMVar_hsa_circ_110999,RMVar_hsa_circ_108787,RMVar_hsa_circ_78709,RMVar_hsa_circ_156328,RMVar_hsa_circ_156327,RMVar_hsa_circ_156330 27533 RMVar_ID_27533 Human_SNP_ID_500589261 A-to-I Human chr12 + 49406300 49406300 49406300 TTCTAGTTTTTGTAAACTTTTTTTTTTTTTTTAAAGACAGGGTCTCTTGCTCTGTTACCTAGGCT TTCTAGTTTTTGTAAACTTTTTTTTTTTTTTTTAAGACAGGGTCTCTTGCTCTGTTACCTAGGCT A T SPATS2 Ensembl:ENSG00000123352 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1219888780 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11955909,Human_RBP_ID_17561095 Human_miRNA_ID_1950701,Human_miRNA_ID_1951988,Human_miRNA_ID_2444148 RMVar_hsa_circ_67313,RMVar_hsa_circ_110999,RMVar_hsa_circ_108787,RMVar_hsa_circ_78709,RMVar_hsa_circ_156328,RMVar_hsa_circ_156327,RMVar_hsa_circ_156330 27534 RMVar_ID_27534 Human_SNP_ID_500593198 A-to-I Human chr12 + 49423274 49423274 49423274 CCTGCCTCAGCCTCCCGAGTAGCCAGGACTACAGGCACGCACCACCACACCAGATAATTTTTGTA CCTGCCTCAGCCTCCCGAGTAGCCAGGACTACGGGCACGCACCACCACACCAGATAATTTTTGTA A G SPATS2 Ensembl:ENSG00000123352 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs962105750 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67313,RMVar_hsa_circ_110999,RMVar_hsa_circ_108787,RMVar_hsa_circ_78709,RMVar_hsa_circ_156328,RMVar_hsa_circ_156327,RMVar_hsa_circ_156330 27535 RMVar_ID_27535 Human_SNP_ID_500595049 A-to-I Human chr12 + 49430914 49430914 49430914 TAGTGATGGAGTTTCACCATGTTGGCCGGGCTAATCTCGAACTCCTGACCTCAAATGATCCACCC TAGTGATGGAGTTTCACCATGTTGGCCGGGCTGATCTCGAACTCCTGACCTCAAATGATCCACCC A G SPATS2 Ensembl:ENSG00000123352 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1265431942 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67313,RMVar_hsa_circ_110999,RMVar_hsa_circ_108787,RMVar_hsa_circ_78709,RMVar_hsa_circ_156328,RMVar_hsa_circ_156327,RMVar_hsa_circ_156330 27536 RMVar_ID_27536 Human_SNP_ID_500601041 A-to-I Human chr12 + 49453738 49453736 49453739 AGCAGGCTAAGACAGAAGAATCGCTTGAGCCCAGGAGTTTGAGGTTGCAGTGAGCTATGATCGTG AGCAGGCTAAGACAGAAGAATCGCTTGAGCC___GAGTTTGAGGTTGCAGTGAGCTATGATCGTG CCAG C SPATS2 Ensembl:ENSG00000123352 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs763336409 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_67313,RMVar_hsa_circ_110999,RMVar_hsa_circ_108787,RMVar_hsa_circ_78709,RMVar_hsa_circ_156328,RMVar_hsa_circ_156327,RMVar_hsa_circ_354297,RMVar_hsa_circ_156330 27537 RMVar_ID_27537 Human_SNP_ID_500601042 A-to-I Human chr12 + 49453738 49453738 49453738 AGCAGGCTAAGACAGAAGAATCGCTTGAGCCCAGGAGTTTGAGGTTGCAGTGAGCTATGATCGTG AGCAGGCTAAGACAGAAGAATCGCTTGAGCCCGGGAGTTTGAGGTTGCAGTGAGCTATGATCGTG A G SPATS2 Ensembl:ENSG00000123352 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1340571909 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67313,RMVar_hsa_circ_110999,RMVar_hsa_circ_108787,RMVar_hsa_circ_78709,RMVar_hsa_circ_156328,RMVar_hsa_circ_156327,RMVar_hsa_circ_354297,RMVar_hsa_circ_156330 27538 RMVar_ID_27538 Human_SNP_ID_500604936 A-to-I Human chr12 + 49468660 49468660 49468660 CATCATGCCTGGCTAATTTTTGTATTTTTTGTAGAGATGTGGTTTCACCATGTTACCCAGGCTGG CATCATGCCTGGCTAATTTTTGTATTTTTTGTGGAGATGTGGTTTCACCATGTTACCCAGGCTGG A G SPATS2 Ensembl:ENSG00000123352 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs919079488 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12082354,Human_RBP_ID_19825372 RMVar_hsa_circ_67313,RMVar_hsa_circ_108787,RMVar_hsa_circ_156335,RMVar_hsa_circ_308868,RMVar_hsa_circ_78709,RMVar_hsa_circ_156327,RMVar_hsa_circ_156330,RMVar_hsa_circ_358360,RMVar_hsa_circ_359914,RMVar_hsa_circ_311656,RMVar_hsa_circ_305229,RMVar_hsa_circ_306642,RMVar_hsa_circ_156333,RMVar_hsa_circ_156334,RMVar_hsa_circ_156332 27539 RMVar_ID_27539 Human_SNP_ID_500604942 A-to-I Human chr12 + 49468682 49468682 49468682 TATTTTTTGTAGAGATGTGGTTTCACCATGTTACCCAGGCTGGCCTCGAACTCCTTGGCTCACAT TATTTTTTGTAGAGATGTGGTTTCACCATGTTGCCCAGGCTGGCCTCGAACTCCTTGGCTCACAT A G SPATS2 Ensembl:ENSG00000123352 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs879443919 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6191093,Human_RBP_ID_11956553,Human_RBP_ID_19825372 RMVar_hsa_circ_67313,RMVar_hsa_circ_108787,RMVar_hsa_circ_156335,RMVar_hsa_circ_308868,RMVar_hsa_circ_78709,RMVar_hsa_circ_156327,RMVar_hsa_circ_156330,RMVar_hsa_circ_358360,RMVar_hsa_circ_359914,RMVar_hsa_circ_311656,RMVar_hsa_circ_305229,RMVar_hsa_circ_306642,RMVar_hsa_circ_156333,RMVar_hsa_circ_156334,RMVar_hsa_circ_156332 27540 RMVar_ID_27540 Human_SNP_ID_500605346 A-to-I Human chr12 + 49470173 49470173 49470173 CCTGTCTCAGCCTCCCTAGTAGCTGGGATTACAGACGTCCACCACCACGCCCAGCTAATTTTTGT CCTGTCTCAGCCTCCCTAGTAGCTGGGATTACCGACGTCCACCACCACGCCCAGCTAATTTTTGT A C SPATS2 Ensembl:ENSG00000123352 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs538770180 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67313,RMVar_hsa_circ_108787,RMVar_hsa_circ_156335,RMVar_hsa_circ_308868,RMVar_hsa_circ_78709,RMVar_hsa_circ_156327,RMVar_hsa_circ_156330,RMVar_hsa_circ_358360,RMVar_hsa_circ_359914,RMVar_hsa_circ_311656,RMVar_hsa_circ_305229,RMVar_hsa_circ_306642,RMVar_hsa_circ_156333,RMVar_hsa_circ_156334,RMVar_hsa_circ_156332 27541 RMVar_ID_27541 Human_SNP_ID_500605357 A-to-I Human chr12 + 49470212 49470212 49470212 CACCACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGTTTTCATCATGTTGGCCAGGC CACCACCACGCCCAGCTAATTTTTGTATTTTTGGTAGAGACGGGTTTTCATCATGTTGGCCAGGC A G SPATS2 Ensembl:ENSG00000123352 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1272638426 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67313,RMVar_hsa_circ_108787,RMVar_hsa_circ_156335,RMVar_hsa_circ_308868,RMVar_hsa_circ_78709,RMVar_hsa_circ_156327,RMVar_hsa_circ_156330,RMVar_hsa_circ_358360,RMVar_hsa_circ_359914,RMVar_hsa_circ_311656,RMVar_hsa_circ_305229,RMVar_hsa_circ_306642,RMVar_hsa_circ_156333,RMVar_hsa_circ_156334,RMVar_hsa_circ_156332 27542 RMVar_ID_27542 Human_SNP_ID_500605575 A-to-I Human chr12 + 49471375 49471375 49471375 TATTATTATCTTTTGAGACAGAGCCTTGCTCCATCAACCAGGCTGAAATGCAGTGGCACAGTCAG TATTATTATCTTTTGAGACAGAGCCTTGCTCCGTCAACCAGGCTGAAATGCAGTGGCACAGTCAG A G SPATS2 Ensembl:ENSG00000123352 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs928772968 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67313,RMVar_hsa_circ_108787,RMVar_hsa_circ_156335,RMVar_hsa_circ_308868,RMVar_hsa_circ_78709,RMVar_hsa_circ_156327,RMVar_hsa_circ_156330,RMVar_hsa_circ_358360,RMVar_hsa_circ_359914,RMVar_hsa_circ_311656,RMVar_hsa_circ_305229,RMVar_hsa_circ_306642,RMVar_hsa_circ_156333,RMVar_hsa_circ_156334,RMVar_hsa_circ_156332 27543 RMVar_ID_27543 Human_SNP_ID_500605588 A-to-I Human chr12 + 49471441 49471441 49471441 TCACTGCAGCCTCAAACATTTGAGCTCAAGCGATCATCCTGCCTTAGCCTCTTGAGTAGCTGAGA TCACTGCAGCCTCAAACATTTGAGCTCAAGCGTTCATCCTGCCTTAGCCTCTTGAGTAGCTGAGA A T SPATS2 Ensembl:ENSG00000123352 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs999437762 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67313,RMVar_hsa_circ_108787,RMVar_hsa_circ_156335,RMVar_hsa_circ_308868,RMVar_hsa_circ_78709,RMVar_hsa_circ_156327,RMVar_hsa_circ_156330,RMVar_hsa_circ_358360,RMVar_hsa_circ_359914,RMVar_hsa_circ_311656,RMVar_hsa_circ_305229,RMVar_hsa_circ_306642,RMVar_hsa_circ_156333,RMVar_hsa_circ_156334,RMVar_hsa_circ_156332 27544 RMVar_ID_27544 Human_SNP_ID_500605604 A-to-I Human chr12 + 49471513 49471513 49471513 AAAGCACCTTGCTAATTTTTTAAAAAATTTTTATAGAGACAGGATCTCACTGTGTTGCCTAAGCA AAAGCACCTTGCTAATTTTTTAAAAAATTTTTGTAGAGACAGGATCTCACTGTGTTGCCTAAGCA A G SPATS2 Ensembl:ENSG00000123352 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs142869251 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67313,RMVar_hsa_circ_108787,RMVar_hsa_circ_156335,RMVar_hsa_circ_308868,RMVar_hsa_circ_78709,RMVar_hsa_circ_156327,RMVar_hsa_circ_156330,RMVar_hsa_circ_358360,RMVar_hsa_circ_359914,RMVar_hsa_circ_311656,RMVar_hsa_circ_305229,RMVar_hsa_circ_306642,RMVar_hsa_circ_156333,RMVar_hsa_circ_156334,RMVar_hsa_circ_156332 27545 RMVar_ID_27545 Human_SNP_ID_500605605 A-to-I Human chr12 + 49471513 49471513 49471513 AAAGCACCTTGCTAATTTTTTAAAAAATTTTTATAGAGACAGGATCTCACTGTGTTGCCTAAGCA AAAGCACCTTGCTAATTTTTTAAAAAATTTTTTTAGAGACAGGATCTCACTGTGTTGCCTAAGCA A T SPATS2 Ensembl:ENSG00000123352 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs142869251 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67313,RMVar_hsa_circ_108787,RMVar_hsa_circ_156335,RMVar_hsa_circ_308868,RMVar_hsa_circ_78709,RMVar_hsa_circ_156327,RMVar_hsa_circ_156330,RMVar_hsa_circ_358360,RMVar_hsa_circ_359914,RMVar_hsa_circ_311656,RMVar_hsa_circ_305229,RMVar_hsa_circ_306642,RMVar_hsa_circ_156333,RMVar_hsa_circ_156334,RMVar_hsa_circ_156332 27546 RMVar_ID_27546 Human_SNP_ID_500605609 A-to-I Human chr12 + 49471549 49471549 49471549 AGACAGGATCTCACTGTGTTGCCTAAGCAGGTATCAAGTTTTAGGTTTCAAGTGATCTTCCTGGC AGACAGGATCTCACTGTGTTGCCTAAGCAGGTGTCAAGTTTTAGGTTTCAAGTGATCTTCCTGGC A G SPATS2 Ensembl:ENSG00000123352 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs886748269 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67313,RMVar_hsa_circ_108787,RMVar_hsa_circ_156335,RMVar_hsa_circ_308868,RMVar_hsa_circ_78709,RMVar_hsa_circ_156327,RMVar_hsa_circ_156330,RMVar_hsa_circ_358360,RMVar_hsa_circ_359914,RMVar_hsa_circ_311656,RMVar_hsa_circ_305229,RMVar_hsa_circ_306642,RMVar_hsa_circ_156333,RMVar_hsa_circ_156334,RMVar_hsa_circ_156332 27547 RMVar_ID_27547 Human_SNP_ID_500606041 A-to-I Human chr12 + 49473341 49473340 49473341 GGGAGGCTGAGACAGTAGAATCACTTGAGCCCAAGAGGTGGAGGTTGCAGTGAGCTGAGATCACA GGGAGGCTGAGACAGTAGAATCACTTGAGCCC_AGAGGTGGAGGTTGCAGTGAGCTGAGATCACA CA C SPATS2 Ensembl:ENSG00000123352 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1349847386 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_24974619 RMVar_hsa_circ_67313,RMVar_hsa_circ_108787,RMVar_hsa_circ_156335,RMVar_hsa_circ_308868,RMVar_hsa_circ_78709,RMVar_hsa_circ_156327,RMVar_hsa_circ_156330,RMVar_hsa_circ_358360,RMVar_hsa_circ_359914,RMVar_hsa_circ_311656,RMVar_hsa_circ_305229,RMVar_hsa_circ_306642,RMVar_hsa_circ_156333,RMVar_hsa_circ_156334,RMVar_hsa_circ_156332 27548 RMVar_ID_27548 Human_SNP_ID_500607792 A-to-I Human chr12 + 49481567 49481567 49481567 TCAGCTCACTGCAACCTCTGCCTCCCGGGTTCAAGCAATTCTCCTGCTTCAGCCTCCCCAGTAGC TCAGCTCACTGCAACCTCTGCCTCCCGGGTTCGAGCAATTCTCCTGCTTCAGCCTCCCCAGTAGC A G SPATS2 Ensembl:ENSG00000123352 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1370210078 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67313,RMVar_hsa_circ_108787,RMVar_hsa_circ_156335,RMVar_hsa_circ_308868,RMVar_hsa_circ_78709,RMVar_hsa_circ_156327,RMVar_hsa_circ_156330,RMVar_hsa_circ_358360,RMVar_hsa_circ_359914,RMVar_hsa_circ_311656,RMVar_hsa_circ_305229,RMVar_hsa_circ_306642,RMVar_hsa_circ_156333,RMVar_hsa_circ_156334,RMVar_hsa_circ_156332 27549 RMVar_ID_27549 Human_SNP_ID_500607799 A-to-I Human chr12 + 49481607 49481607 49481607 CTCCTGCTTCAGCCTCCCCAGTAGCTGGAATTACAGGTGCCTGCCACCATGCCTGGCTAATTTTT CTCCTGCTTCAGCCTCCCCAGTAGCTGGAATTGCAGGTGCCTGCCACCATGCCTGGCTAATTTTT A G SPATS2 Ensembl:ENSG00000123352 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1215050824 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67313,RMVar_hsa_circ_108787,RMVar_hsa_circ_156335,RMVar_hsa_circ_308868,RMVar_hsa_circ_78709,RMVar_hsa_circ_156327,RMVar_hsa_circ_156330,RMVar_hsa_circ_358360,RMVar_hsa_circ_359914,RMVar_hsa_circ_311656,RMVar_hsa_circ_305229,RMVar_hsa_circ_306642,RMVar_hsa_circ_156333,RMVar_hsa_circ_156334,RMVar_hsa_circ_156332 27550 RMVar_ID_27550 Human_SNP_ID_500608110 A-to-I Human chr12 + 49483063 49483063 49483063 CACCTGCCTTGGCCTCCCAAAATGTTCGGATTATAGGCGTGAACCACCACACCCAGCCTTTCCTT CACCTGCCTTGGCCTCCCAAAATGTTCGGATTCTAGGCGTGAACCACCACACCCAGCCTTTCCTT A C SPATS2 Ensembl:ENSG00000123352 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1311586442 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11956836 RMVar_hsa_circ_67313,RMVar_hsa_circ_108787,RMVar_hsa_circ_156335,RMVar_hsa_circ_308868,RMVar_hsa_circ_78709,RMVar_hsa_circ_156327,RMVar_hsa_circ_156330,RMVar_hsa_circ_358360,RMVar_hsa_circ_359914,RMVar_hsa_circ_311656,RMVar_hsa_circ_305229,RMVar_hsa_circ_306642,RMVar_hsa_circ_156333,RMVar_hsa_circ_156334,RMVar_hsa_circ_156332 27551 RMVar_ID_27551 Human_SNP_ID_500609373 A-to-I Human chr12 + 49488228 49488228 49488228 CACTGTGCCCAACTAATTTTTGTATTTTCAGTAGAGACGGCGTTTTTCCATGTTGGTCAGGCTGG CACTGTGCCCAACTAATTTTTGTATTTTCAGTGGAGACGGCGTTTTTCCATGTTGGTCAGGCTGG A G SPATS2 Ensembl:ENSG00000123352 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1034196858 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11956900 RMVar_hsa_circ_67313,RMVar_hsa_circ_108787,RMVar_hsa_circ_156335,RMVar_hsa_circ_308868,RMVar_hsa_circ_78709,RMVar_hsa_circ_156327,RMVar_hsa_circ_156330,RMVar_hsa_circ_358360,RMVar_hsa_circ_359914,RMVar_hsa_circ_311656,RMVar_hsa_circ_306642,RMVar_hsa_circ_156333,RMVar_hsa_circ_156334,RMVar_hsa_circ_156332,RMVar_hsa_circ_156336,RMVar_hsa_circ_303235,RMVar_hsa_circ_318499,RMVar_hsa_circ_310507 27552 RMVar_ID_27552 Human_SNP_ID_500609961 A-to-I Human chr12 + 49490987 49490987 49490987 AACATGGTGAAGTCCCGTCTCTACTAAAAAATAGAAAAAATTAGCCAGGTGTGGTGGCACGTGCC AACATGGTGAAGTCCCGTCTCTACTAAAAAATGGAAAAAATTAGCCAGGTGTGGTGGCACGTGCC A G SPATS2 Ensembl:ENSG00000123352 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs556398098 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108787,RMVar_hsa_circ_156335,RMVar_hsa_circ_308868,RMVar_hsa_circ_156327,RMVar_hsa_circ_358360,RMVar_hsa_circ_311656,RMVar_hsa_circ_156334,RMVar_hsa_circ_33086,RMVar_hsa_circ_156336,RMVar_hsa_circ_303235,RMVar_hsa_circ_307964,RMVar_hsa_circ_156338 27553 RMVar_ID_27553 Human_SNP_ID_500610305 A-to-I Human chr12 + 49492405 49492405 49492405 ACTGCGCCTGGCTAATATTTGTATTTTTTAGTAGAGACAGGGTTTCACCATGTTGGCTAGGCTGG ACTGCGCCTGGCTAATATTTGTATTTTTTAGTTGAGACAGGGTTTCACCATGTTGGCTAGGCTGG A T SPATS2 Ensembl:ENSG00000123352 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1343098629 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108787,RMVar_hsa_circ_156335,RMVar_hsa_circ_308868,RMVar_hsa_circ_156327,RMVar_hsa_circ_358360,RMVar_hsa_circ_311656,RMVar_hsa_circ_156334,RMVar_hsa_circ_33086,RMVar_hsa_circ_156336,RMVar_hsa_circ_303235,RMVar_hsa_circ_307964,RMVar_hsa_circ_156338 27554 RMVar_ID_27554 Human_SNP_ID_500610331 A-to-I Human chr12 + 49492456 49492456 49492456 GTTGGCTAGGCTGGTGTCGAACGCCTGACCCCAAGTGATCTGCGCACCTTGGCCTCCCAAAGTGC GTTGGCTAGGCTGGTGTCGAACGCCTGACCCCGAGTGATCTGCGCACCTTGGCCTCCCAAAGTGC A G SPATS2 Ensembl:ENSG00000123352 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913753500 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108787,RMVar_hsa_circ_156335,RMVar_hsa_circ_308868,RMVar_hsa_circ_156327,RMVar_hsa_circ_358360,RMVar_hsa_circ_311656,RMVar_hsa_circ_156334,RMVar_hsa_circ_33086,RMVar_hsa_circ_156336,RMVar_hsa_circ_303235,RMVar_hsa_circ_307964,RMVar_hsa_circ_156338 27555 RMVar_ID_27555 Human_SNP_ID_500610422 A-to-I Human chr12 + 49492925 49492925 49492925 TGAGACCAGCCTGGCCAACATGGTGAAACCCTATCTCTACTAAAAATACAAAAAAATTAGCTGGG TGAGACCAGCCTGGCCAACATGGTGAAACCCTGTCTCTACTAAAAATACAAAAAAATTAGCTGGG A G SPATS2 Ensembl:ENSG00000123352 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1332241140 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108787,RMVar_hsa_circ_156335,RMVar_hsa_circ_308868,RMVar_hsa_circ_156327,RMVar_hsa_circ_358360,RMVar_hsa_circ_311656,RMVar_hsa_circ_156334,RMVar_hsa_circ_33086,RMVar_hsa_circ_156336,RMVar_hsa_circ_303235,RMVar_hsa_circ_307964,RMVar_hsa_circ_156338 27556 RMVar_ID_27556 Human_SNP_ID_500613052 A-to-I Human chr12 + 49503188 49503188 49503188 CTTGGCCAACATGGTGAAACCCCATCTCTACTAAACATTCAAAAATTAGCCGGGCGTGGTGGCGT CTTGGCCAACATGGTGAAACCCCATCTCTACTGAACATTCAAAAATTAGCCGGGCGTGGTGGCGT A G SPATS2 Ensembl:ENSG00000123352 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs372950421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11957127 RMVar_hsa_circ_33086,RMVar_hsa_circ_349686,RMVar_hsa_circ_44098,RMVar_hsa_circ_156340,RMVar_hsa_circ_156341,RMVar_hsa_circ_31328,RMVar_hsa_circ_306561,RMVar_hsa_circ_156343 27557 RMVar_ID_27557 Human_SNP_ID_500614237 A-to-I Human chr12 + 49508233 49508233 49508233 CATAATTCCAGTTTCTTTTTTTTTTTAGACTGAGTCTCGTTCTGTCTCCCAGGCCAGAATGTAGT CATAATTCCAGTTTCTTTTTTTTTTTAGACTGGGTCTCGTTCTGTCTCCCAGGCCAGAATGTAGT A G SPATS2 Ensembl:ENSG00000123352 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1344420147 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9687640,Human_RBP_ID_11957203,Human_RBP_ID_23306279 RMVar_hsa_circ_33086,RMVar_hsa_circ_349686,RMVar_hsa_circ_44098,RMVar_hsa_circ_156340,RMVar_hsa_circ_156341,RMVar_hsa_circ_31328,RMVar_hsa_circ_306561,RMVar_hsa_circ_156343 27558 RMVar_ID_27558 Human_SNP_ID_500614331 A-to-I Human chr12 + 49508669 49508669 49508669 GTTACCCAGTCTGGTCTTGACCTCCTGGGCTCAAGTGATCCTCCTGCCTCGACTTCCCCAAGTGC GTTACCCAGTCTGGTCTTGACCTCCTGGGCTCCAGTGATCCTCCTGCCTCGACTTCCCCAAGTGC A C SPATS2 Ensembl:ENSG00000123352 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1386176277 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33086,RMVar_hsa_circ_349686,RMVar_hsa_circ_44098,RMVar_hsa_circ_156340,RMVar_hsa_circ_156341,RMVar_hsa_circ_31328,RMVar_hsa_circ_306561,RMVar_hsa_circ_156343 27559 RMVar_ID_27559 Human_SNP_ID_500614342 A-to-I Human chr12 + 49508715 49508715 49508715 CCTCGACTTCCCCAAGTGCTGGGATAGCAGGCATGAGCCACAGTGCCTGGCCCTGGCTCAGCCTT CCTCGACTTCCCCAAGTGCTGGGATAGCAGGCGTGAGCCACAGTGCCTGGCCCTGGCTCAGCCTT A G SPATS2 Ensembl:ENSG00000123352 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1036009795 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25023714 RMVar_hsa_circ_33086,RMVar_hsa_circ_349686,RMVar_hsa_circ_44098,RMVar_hsa_circ_156340,RMVar_hsa_circ_156341,RMVar_hsa_circ_31328,RMVar_hsa_circ_306561,RMVar_hsa_circ_156343 27560 RMVar_ID_27560 Human_SNP_ID_500614393 A-to-I Human chr12 + 49508984 49508984 49508984 TACTTGGGAGGCTGAGACAGGAAAATTGCTTGAACCGGGGACGCAAAGGTTGCAGTGAGCCGAGA TACTTGGGAGGCTGAGACAGGAAAATTGCTTGCACCGGGGACGCAAAGGTTGCAGTGAGCCGAGA A C SPATS2 Ensembl:ENSG00000123352 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs764108383 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33086,RMVar_hsa_circ_349686,RMVar_hsa_circ_44098,RMVar_hsa_circ_156340,RMVar_hsa_circ_156341,RMVar_hsa_circ_31328,RMVar_hsa_circ_306561,RMVar_hsa_circ_156343 27561 RMVar_ID_27561 Human_SNP_ID_500614544 A-to-I Human chr12 + 49509449 49509449 49509449 ATTACAGGCGCACGCCACATTTTTGTACTTCTAGTAGAGACAGGGTTTCATCATATTGGCCAGGC ATTACAGGCGCACGCCACATTTTTGTACTTCTGGTAGAGACAGGGTTTCATCATATTGGCCAGGC A G SPATS2 Ensembl:ENSG00000123352 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1278005763 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33086,RMVar_hsa_circ_349686,RMVar_hsa_circ_44098,RMVar_hsa_circ_156340,RMVar_hsa_circ_156341,RMVar_hsa_circ_31328,RMVar_hsa_circ_306561,RMVar_hsa_circ_156343 27562 RMVar_ID_27562 Human_SNP_ID_500614546 A-to-I Human chr12 + 49509452 49509452 49509452 ACAGGCGCACGCCACATTTTTGTACTTCTAGTAGAGACAGGGTTTCATCATATTGGCCAGGCATC ACAGGCGCACGCCACATTTTTGTACTTCTAGTGGAGACAGGGTTTCATCATATTGGCCAGGCATC A G SPATS2 Ensembl:ENSG00000123352 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1341169306 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33086,RMVar_hsa_circ_349686,RMVar_hsa_circ_44098,RMVar_hsa_circ_156340,RMVar_hsa_circ_156341,RMVar_hsa_circ_31328,RMVar_hsa_circ_306561,RMVar_hsa_circ_156343 27563 RMVar_ID_27563 Human_SNP_ID_500614802 A-to-I Human chr12 + 49510425 49510425 49510425 TCTCTACAAAAAATGTAAAAAATTAGCTGGGCATGGTAGCTCGTGCCTGTAGTCCCAGCTACTTA TCTCTACAAAAAATGTAAAAAATTAGCTGGGCGTGGTAGCTCGTGCCTGTAGTCCCAGCTACTTA A G SPATS2 Ensembl:ENSG00000123352 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs916675172 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33086,RMVar_hsa_circ_349686,RMVar_hsa_circ_44098,RMVar_hsa_circ_156340,RMVar_hsa_circ_156341,RMVar_hsa_circ_31328,RMVar_hsa_circ_306561,RMVar_hsa_circ_156343 27564 RMVar_ID_27564 Human_SNP_ID_500622354 A-to-I Human chr12 + 49540182 49540182 49540182 CATCCCCCGTGGGGCTTCCCAGCTCTCTGCCTAGGTCCTCCTTGGTCTCCGGTTCCTGATAGGGG CATCCCCCGTGGGGCTTCCCAGCTCTCTGCCTGGGTCCTCCTTGGTCTCCGGTTCCTGATAGGGG A G KCNH3 Ensembl:ENSG00000135519 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1287500388 Functional Loss SNV dbSNP153 33..33 33 - - - 27565 RMVar_ID_27565 Human_SNP_ID_500629657 A-to-I Human chr12 - 49565530 49565529 49565530 GGGGAGTGAACCCTCCTCCAGTGAGAAGAAGAAGGTGAGGAATTGGGAGACTTAGGGGATGGGAG GGGGAGTGAACCCTCCTCCAGTGAGAAGAAGA_GGTGAGGAATTGGGAGACTTAGGGGATGGGAG CT C MCRS1 Ensembl:ENSG00000187778 Protein coding 5'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs763871870 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_9344503 Human_Splice_Rec_1365101,Human_Splice_Rec_1365129,Human_Splice_Rec_1365153,Human_Splice_Rec_1365179,Human_Splice_Rec_1365209,Human_Splice_Rec_1365259,Human_Splice_Rec_1365287,Human_Splice_Rec_1365307,Human_Splice_Rec_1365319,Human_Splice_Rec_1365329 RMVar_hsa_circ_120368,RMVar_hsa_circ_156351,RMVar_hsa_circ_156352,RMVar_hsa_circ_117931 27566 RMVar_ID_27566 Human_SNP_ID_500631494 A-to-I Human chr12 + 49572766 49572766 49572766 TAGGCTCTGACCAGACCTGGGAGCTCACGCCTATAATCCCAGCATGGTGGGAGGCCGAGGCGGGC TAGGCTCTGACCAGACCTGGGAGCTCACGCCTGTAATCCCAGCATGGTGGGAGGCCGAGGCGGGC A G PRPF40B Ensembl:ENSG00000110844 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1420133761 Functional Loss SNV dbSNP153 33..33 33 - - - 27567 RMVar_ID_27567 Human_SNP_ID_500632815 A-to-I Human chr12 + 49579081 49579081 49579081 GAGTGCAATGATCTCGGCTCACTTGAATCTCCACTTCCCAAATTCAAGCGATTCTCCTGCCTCAG GAGTGCAATGATCTCGGCTCACTTGAATCTCCGCTTCCCAAATTCAAGCGATTCTCCTGCCTCAG A G PRPF40B Ensembl:ENSG00000110844 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs536617658 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11957764 27568 RMVar_ID_27568 Human_SNP_ID_500636609 A-to-I Human chr12 + 49595326 49595324 49595327 GAAGATGCAAAAAAAGAGGGACCATATGACATAGTAGTTCTACCAGGAGGTAATCTGGGTGCACA GAAGATGCAAAAAAAGAGGGACCATATGACA___TAGTTCTACCAGGAGGTAATCTGGGTGCACA ATAG A PRPF40B,AC020612.1 Ensembl:ENSG00000110844,Ensembl:ENSG00000257243 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs371561985 Functional Loss DEL dbSNP153 32..34 33 - - - 27569 RMVar_ID_27569 Human_SNP_ID_500636610 A-to-I Human chr12 + 49595324 49595324 49595324 TTGAAGATGCAAAAAAAGAGGGACCATATGACATAGTAGTTCTACCAGGAGGTAATCTGGGTGCA TTGAAGATGCAAAAAAAGAGGGACCATATGACGTAGTAGTTCTACCAGGAGGTAATCTGGGTGCA A G PRPF40B,AC020612.1 Ensembl:ENSG00000110844,Ensembl:ENSG00000257243 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs950289391 Functional Loss SNV dbSNP153 33..33 33 - - - 27570 RMVar_ID_27570 Human_SNP_ID_500636611 A-to-I Human chr12 + 49595326 49595326 49595326 GAAGATGCAAAAAAAGAGGGACCATATGACATAGTAGTTCTACCAGGAGGTAATCTGGGTGCACA GAAGATGCAAAAAAAGAGGGACCATATGACATGGTAGTTCTACCAGGAGGTAATCTGGGTGCACA A G PRPF40B,AC020612.1 Ensembl:ENSG00000110844,Ensembl:ENSG00000257243 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903468212 Functional Loss SNV dbSNP153 33..33 33 - - - 27571 RMVar_ID_27571 Human_SNP_ID_500636612 A-to-I Human chr12 + 49595329 49595329 49595329 GATGCAAAAAAAGAGGGACCATATGACATAGTAGTTCTACCAGGAGGTAATCTGGGTGCACAGAA GATGCAAAAAAAGAGGGACCATATGACATAGTGGTTCTACCAGGAGGTAATCTGGGTGCACAGAA A G PRPF40B,AC020612.1 Ensembl:ENSG00000110844,Ensembl:ENSG00000257243 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs999125423 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17581815 27572 RMVar_ID_27572 Human_SNP_ID_500675141 A-to-I Human chr12 - 49753027 49753027 49753027 TGGACATAGGCCCCTGCAGCCGCCACAAACATACAAAGGGCAAAACTTGCATAGACCTTCTTCAG TGGACATAGGCCCCTGCAGCCGCCACAAACATCCAAAGGGCAAAACTTGCATAGACCTTCTTCAG T G - - Other Unknown GSE56152 embryonic stem cells,wild type - 25708366 RNA-Seq:(High) rs751487929 Functional Loss SNV dbSNP153 33..33 33 - - - 27573 RMVar_ID_27573 Human_SNP_ID_500677505 A-to-I Human chr12 + 49760717 49760717 49760717 CTCCACCACGTCCAGCTAATTTCTGTAATTTTAGTAGAACGAGGTTTTGCCACGTTGCCCCGTGA CTCCACCACGTCCAGCTAATTTCTGTAATTTTTGTAGAACGAGGTTTTGCCACGTTGCCCCGTGA A T TMBIM6 Ensembl:ENSG00000139644 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1030065680 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6191707,Human_RBP_ID_11958828 RMVar_hsa_circ_123454,RMVar_hsa_circ_156369,RMVar_hsa_circ_156372,RMVar_hsa_circ_125329 27574 RMVar_ID_27574 Human_SNP_ID_500683750 A-to-I Human chr12 - 49785088 49785088 49785088 GGAGGATCCCTTGAGCCCAGAAGTTTGAGGCTACAGCAAGCTATTTTCCTACCACTGCACTCCAG GGAGGATCCCTTGAGCCCAGAAGTTTGAGGCTGCAGCAAGCTATTTTCCTACCACTGCACTCCAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs936866969 Functional Loss SNV dbSNP153 33..33 33 - - - 27575 RMVar_ID_27575 Human_SNP_ID_500683794 A-to-I Human chr12 - 49785297 49785297 49785297 TAAGATAAATTCCTATATTCTCCAGGTATAGTAGCTCATGCCAGTAATTTTAGCACTTTGAAAGG TAAGATAAATTCCTATATTCTCCAGGTATAGTGGCTCATGCCAGTAATTTTAGCACTTTGAAAGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs752800858 Functional Loss SNV dbSNP153 33..33 33 - - - 27576 RMVar_ID_27576 Human_SNP_ID_515537662 A-to-I Human chr12 + 110013677 110013677 110013677 CCTGTAGTCTGAGCTACTTGGGAGGCTGAGGTAGGATGATCGCTTGAACCCAGAAGGTTGAGGCT CCTGTAGTCTGAGCTACTTGGGAGGCTGAGGTGGGATGATCGCTTGAACCCAGAAGGTTGAGGCT A G ANKRD13A Ensembl:ENSG00000076513 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1045074713 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7541,RMVar_hsa_circ_48664,RMVar_hsa_circ_273070,RMVar_hsa_circ_358120,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_159762,RMVar_hsa_circ_159763 27577 RMVar_ID_27577 Human_SNP_ID_515573997 A-to-I Human chr12 + 110168060 110168060 110168060 TTTGTTTTGTTTTGTAGAGATGTGGTCTCACTATGTTTCCCAGGCTGGTCTTAAACTCCCGGCCT TTTGTTTTGTTTTGTAGAGATGTGGTCTCACTGTGTTTCCCAGGCTGGTCTTAAACTCCCGGCCT A G IFT81 Ensembl:ENSG00000122970 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs969228356 Functional Loss SNV 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_159798,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_159811,RMVar_hsa_circ_26653,RMVar_hsa_circ_265767,RMVar_hsa_circ_323000 27578 RMVar_ID_27578 Human_SNP_ID_515578994 A-to-I Human chr12 + 110188238 110188238 110188238 CCGGGAATCCCAGCTGCTCGGGAGGCTGAGGCAGGAGAATGGCATGAACCTGGGAGGCGGAGGTT CCGGGAATCCCAGCTGCTCGGGAGGCTGAGGCGGGAGAATGGCATGAACCTGGGAGGCGGAGGTT A G IFT81 Ensembl:ENSG00000122970 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1323268518 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_159793,RMVar_hsa_circ_326158,RMVar_hsa_circ_339487,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_334095,RMVar_hsa_circ_342917,RMVar_hsa_circ_324233,RMVar_hsa_circ_14206,RMVar_hsa_circ_15104,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_159812,RMVar_hsa_circ_56318,RMVar_hsa_circ_26653,RMVar_hsa_circ_265767,RMVar_hsa_circ_323000,RMVar_hsa_circ_307516,RMVar_hsa_circ_365303,RMVar_hsa_circ_267615,RMVar_hsa_circ_28358 27579 RMVar_ID_27579 Human_SNP_ID_515593735 A-to-I Human chr12 + 110255335 110255335 110255335 TTTTTGAGACAATGTCTCGCTCTGCCCAGGCTAAAGTGCAGTGGTGCAGTCACGGCTCACTGCAG TTTTTGAGACAATGTCTCGCTCTGCCCAGGCTCAAGTGCAGTGGTGCAGTCACGGCTCACTGCAG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs537823414 Functional Loss SNV dbSNP153 33..33 33 - - - 27580 RMVar_ID_27580 Human_SNP_ID_515593736 A-to-I Human chr12 + 110255335 110255335 110255335 TTTTTGAGACAATGTCTCGCTCTGCCCAGGCTAAAGTGCAGTGGTGCAGTCACGGCTCACTGCAG TTTTTGAGACAATGTCTCGCTCTGCCCAGGCTGAAGTGCAGTGGTGCAGTCACGGCTCACTGCAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs537823414 Functional Loss SNV dbSNP153 33..33 33 - - - 27581 RMVar_ID_27581 Human_SNP_ID_515598686 A-to-I Human chr12 + 110277023 110277023 110277023 CGGGGCTTCACCATGTTGGCCAGGCTGGTCTCAAACTCCTGACCTCATGTGGTCCACCCGCTTGG CGGGGCTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCATGTGGTCCACCCGCTTGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025763630 Functional Loss SNV dbSNP153 33..33 33 - - - 27582 RMVar_ID_27582 Human_SNP_ID_515601645 A-to-I Human chr12 + 110287868 110287868 110287868 CAGCTCCTGGCCTTAGGTGATCCGCCTGCCTCAGCTTCCCAAAGTGCTGGGATTACAGACATGAG CAGCTCCTGGCCTTAGGTGATCCGCCTGCCTCGGCTTCCCAAAGTGCTGGGATTACAGACATGAG A G ATP2A2 Ensembl:ENSG00000174437 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1379053372 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75481,RMVar_hsa_circ_268494 27583 RMVar_ID_27583 Human_SNP_ID_515601833 A-to-I Human chr12 + 110288484 110288483 110288484 TGGAGTGCAATGGCGCGATCTCGGCTCGCTGTAACCTCTGCCTCCCGGGGTCAAGCGATTCTCCT TGGAGTGCAATGGCGCGATCTCGGCTCGCTGT_ACCTCTGCCTCCCGGGGTCAAGCGATTCTCCT TA T ATP2A2 Ensembl:ENSG00000174437 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs539883631 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_11802959 RMVar_hsa_circ_75481,RMVar_hsa_circ_268494 27584 RMVar_ID_27584 Human_SNP_ID_515601834 A-to-I Human chr12 + 110288484 110288484 110288484 TGGAGTGCAATGGCGCGATCTCGGCTCGCTGTAACCTCTGCCTCCCGGGGTCAAGCGATTCTCCT TGGAGTGCAATGGCGCGATCTCGGCTCGCTGTGACCTCTGCCTCCCGGGGTCAAGCGATTCTCCT A G ATP2A2 Ensembl:ENSG00000174437 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs567531571 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11802959 RMVar_hsa_circ_75481,RMVar_hsa_circ_268494 27585 RMVar_ID_27585 Human_SNP_ID_515603012 A-to-I Human chr12 + 110292666 110292666 110292666 ATTCTTCGCCAAGTGTGGTGGCACCAGCCTGTAGTCTCAGCTACTCAGGAGGCTGAGGTGGGAGG ATTCTTCGCCAAGTGTGGTGGCACCAGCCTGTGGTCTCAGCTACTCAGGAGGCTGAGGTGGGAGG A G ATP2A2 Ensembl:ENSG00000174437 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs995428620 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11803109 RMVar_hsa_circ_75481,RMVar_hsa_circ_159818,RMVar_hsa_circ_159820,RMVar_hsa_circ_284093,RMVar_hsa_circ_339397,RMVar_hsa_circ_268494,RMVar_hsa_circ_325179,RMVar_hsa_circ_101430,RMVar_hsa_circ_159819 27586 RMVar_ID_27586 Human_SNP_ID_515603630 A-to-I Human chr12 + 110294205 110294205 110294205 AGCTGGGATTACAGGTGCCCACCACCACGCCCAGCTAATTTTTTGTACTTTTAATAGAGACGGGG AGCTGGGATTACAGGTGCCCACCACCACGCCCGGCTAATTTTTTGTACTTTTAATAGAGACGGGG A G ATP2A2 Ensembl:ENSG00000174437 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1404523915 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75481,RMVar_hsa_circ_159818,RMVar_hsa_circ_159820,RMVar_hsa_circ_284093,RMVar_hsa_circ_339397,RMVar_hsa_circ_268494,RMVar_hsa_circ_325179,RMVar_hsa_circ_101430,RMVar_hsa_circ_159819 27587 RMVar_ID_27587 Human_SNP_ID_515603695 A-to-I Human chr12 + 110294450 110294450 110294450 GGGAAGCTGAGGCGGGTGGATCAGTTAAGGTCAGGAGGTCGAGACCAGCCTGGCCAACATGGCAA GGGAAGCTGAGGCGGGTGGATCAGTTAAGGTCGGGAGGTCGAGACCAGCCTGGCCAACATGGCAA A G ATP2A2 Ensembl:ENSG00000174437 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1330472298 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75481,RMVar_hsa_circ_159818,RMVar_hsa_circ_159820,RMVar_hsa_circ_284093,RMVar_hsa_circ_339397,RMVar_hsa_circ_268494,RMVar_hsa_circ_325179,RMVar_hsa_circ_101430,RMVar_hsa_circ_159819 27588 RMVar_ID_27588 Human_SNP_ID_515604402 A-to-I Human chr12 + 110297228 110297228 110297228 TTGGGATGCCGAGGCAGGCAGATCACGAGGTCAAGAGATTGAGACCACCCTGGCCAACATGAAAC TTGGGATGCCGAGGCAGGCAGATCACGAGGTCGAGAGATTGAGACCACCCTGGCCAACATGAAAC A G ATP2A2 Ensembl:ENSG00000174437 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1230093878 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11803234 RMVar_hsa_circ_159820,RMVar_hsa_circ_339397,RMVar_hsa_circ_268494,RMVar_hsa_circ_325179,RMVar_hsa_circ_101430,RMVar_hsa_circ_159819,RMVar_hsa_circ_16970,RMVar_hsa_circ_267949,RMVar_hsa_circ_333293,RMVar_hsa_circ_346675,RMVar_hsa_circ_70757,RMVar_hsa_circ_159821 27589 RMVar_ID_27589 Human_SNP_ID_515604420 A-to-I Human chr12 + 110297288 110297288 110297288 GAAACCTCATCTCTACTAAAAATGCAAAAATTAGCCGGGCATGATGGTGTGTGCCTGTAGTCCCA GAAACCTCATCTCTACTAAAAATGCAAAAATTGGCCGGGCATGATGGTGTGTGCCTGTAGTCCCA A G ATP2A2 Ensembl:ENSG00000174437 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs977202196 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_159820,RMVar_hsa_circ_339397,RMVar_hsa_circ_268494,RMVar_hsa_circ_325179,RMVar_hsa_circ_101430,RMVar_hsa_circ_159819,RMVar_hsa_circ_16970,RMVar_hsa_circ_267949,RMVar_hsa_circ_333293,RMVar_hsa_circ_346675,RMVar_hsa_circ_70757,RMVar_hsa_circ_159821 27590 RMVar_ID_27590 Human_SNP_ID_515608469 A-to-I Human chr12 + 110312058 110312058 110312058 AAAATTTGCTGGGCATGTTGACGTGCTCCTGTAGTCCCTGCTTCTCGGGAGGCTGAGGTGGGAGG AAAATTTGCTGGGCATGTTGACGTGCTCCTGTGGTCCCTGCTTCTCGGGAGGCTGAGGTGGGAGG A G ATP2A2 Ensembl:ENSG00000174437 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1412503766 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11803810,Human_RBP_ID_24365991 RMVar_hsa_circ_159820,RMVar_hsa_circ_339397,RMVar_hsa_circ_268494,RMVar_hsa_circ_325179,RMVar_hsa_circ_101430,RMVar_hsa_circ_159819,RMVar_hsa_circ_16970,RMVar_hsa_circ_267949,RMVar_hsa_circ_333293,RMVar_hsa_circ_346675,RMVar_hsa_circ_70757,RMVar_hsa_circ_159821 27591 RMVar_ID_27591 Human_SNP_ID_515608892 A-to-I Human chr12 + 110313535 110313535 110313535 TGGGGTTTCACCATGTTAGCCAGGCTGGTCTCAAACTCCTGACCTCAAGTGCTTCATCTGCCTTG TGGGGTTTCACCATGTTAGCCAGGCTGGTCTCGAACTCCTGACCTCAAGTGCTTCATCTGCCTTG A G ATP2A2 Ensembl:ENSG00000174437 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs926928554 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_159820,RMVar_hsa_circ_339397,RMVar_hsa_circ_268494,RMVar_hsa_circ_325179,RMVar_hsa_circ_101430,RMVar_hsa_circ_159819,RMVar_hsa_circ_16970,RMVar_hsa_circ_267949,RMVar_hsa_circ_333293,RMVar_hsa_circ_346675,RMVar_hsa_circ_70757,RMVar_hsa_circ_159821 27592 RMVar_ID_27592 Human_SNP_ID_515611301 A-to-I Human chr12 + 110323382 110323382 110323382 AATTTTTGTATTTTTATTAGAGATGGGGTTTTACCTTGTTGGTCAGGCTGGTCTTGAACTCCTGA AATTTTTGTATTTTTATTAGAGATGGGGTTTTTCCTTGTTGGTCAGGCTGGTCTTGAACTCCTGA A T ATP2A2 Ensembl:ENSG00000174437 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1386342413 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15765,RMVar_hsa_circ_159820,RMVar_hsa_circ_339397,RMVar_hsa_circ_268494,RMVar_hsa_circ_101430,RMVar_hsa_circ_16970,RMVar_hsa_circ_267949,RMVar_hsa_circ_346675,RMVar_hsa_circ_70757,RMVar_hsa_circ_322827,RMVar_hsa_circ_159821,RMVar_hsa_circ_362077,RMVar_hsa_circ_57837,RMVar_hsa_circ_159822 27593 RMVar_ID_27593 Human_SNP_ID_515611738 A-to-I Human chr12 + 110325014 110325014 110325014 AATTGTATTTTTAGTAGAGATAGGGTTTTGCCATGTTGTCCAGGCTGGTCTTGACCTCCTGACCT AATTGTATTTTTAGTAGAGATAGGGTTTTGCCGTGTTGTCCAGGCTGGTCTTGACCTCCTGACCT A G ATP2A2 Ensembl:ENSG00000174437 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs915384325 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11804080,Human_RBP_ID_17561502 RMVar_hsa_circ_15765,RMVar_hsa_circ_159820,RMVar_hsa_circ_339397,RMVar_hsa_circ_268494,RMVar_hsa_circ_101430,RMVar_hsa_circ_16970,RMVar_hsa_circ_267949,RMVar_hsa_circ_346675,RMVar_hsa_circ_70757,RMVar_hsa_circ_322827,RMVar_hsa_circ_159821,RMVar_hsa_circ_362077,RMVar_hsa_circ_57837,RMVar_hsa_circ_159822 27594 RMVar_ID_27594 Human_SNP_ID_515611758 A-to-I Human chr12 + 110325095 110325095 110325095 TCAAACCCCCAAAGTGCTGGGATTACAGACATAAGTCATCACACCCAGCCTATAATAAAAAACTT TCAAACCCCCAAAGTGCTGGGATTACAGACATGAGTCATCACACCCAGCCTATAATAAAAAACTT A G ATP2A2 Ensembl:ENSG00000174437 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1055093150 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15765,RMVar_hsa_circ_159820,RMVar_hsa_circ_339397,RMVar_hsa_circ_268494,RMVar_hsa_circ_101430,RMVar_hsa_circ_16970,RMVar_hsa_circ_267949,RMVar_hsa_circ_346675,RMVar_hsa_circ_70757,RMVar_hsa_circ_322827,RMVar_hsa_circ_159821,RMVar_hsa_circ_362077,RMVar_hsa_circ_57837,RMVar_hsa_circ_159822 27595 RMVar_ID_27595 Human_SNP_ID_515611831 A-to-I Human chr12 + 110325370 110325370 110325370 TTTAAATTGAAATCAGCTGGGCATGGTGTCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAG TTTAAATTGAAATCAGCTGGGCATGGTGTCTCGTGCCTGTAATCCCAGCACTTTGGGAGGCCGAG A G ATP2A2 Ensembl:ENSG00000174437 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1403302038 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15765,RMVar_hsa_circ_159820,RMVar_hsa_circ_339397,RMVar_hsa_circ_268494,RMVar_hsa_circ_101430,RMVar_hsa_circ_16970,RMVar_hsa_circ_267949,RMVar_hsa_circ_346675,RMVar_hsa_circ_70757,RMVar_hsa_circ_322827,RMVar_hsa_circ_159821,RMVar_hsa_circ_362077,RMVar_hsa_circ_57837,RMVar_hsa_circ_159822 27596 RMVar_ID_27596 Human_SNP_ID_515611857 A-to-I Human chr12 + 110325419 110325419 110325419 ACTTTGGGAGGCCGAGGTGGGGGGATCACCTCAGGTCAGGAGTTTGAGACCAGCCTTGGCCAACA ACTTTGGGAGGCCGAGGTGGGGGGATCACCTCGGGTCAGGAGTTTGAGACCAGCCTTGGCCAACA A G ATP2A2 Ensembl:ENSG00000174437 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1261105429 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15765,RMVar_hsa_circ_159820,RMVar_hsa_circ_339397,RMVar_hsa_circ_268494,RMVar_hsa_circ_101430,RMVar_hsa_circ_16970,RMVar_hsa_circ_267949,RMVar_hsa_circ_346675,RMVar_hsa_circ_70757,RMVar_hsa_circ_322827,RMVar_hsa_circ_159821,RMVar_hsa_circ_362077,RMVar_hsa_circ_57837,RMVar_hsa_circ_159822 27597 RMVar_ID_27597 Human_SNP_ID_515611866 A-to-I Human chr12 + 110325451 110325451 110325451 AGGTCAGGAGTTTGAGACCAGCCTTGGCCAACATAGCAAAACCTGTCTCTACTAAAAATACAAAA AGGTCAGGAGTTTGAGACCAGCCTTGGCCAACGTAGCAAAACCTGTCTCTACTAAAAATACAAAA A G ATP2A2 Ensembl:ENSG00000174437 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs991251432 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15765,RMVar_hsa_circ_159820,RMVar_hsa_circ_339397,RMVar_hsa_circ_268494,RMVar_hsa_circ_101430,RMVar_hsa_circ_16970,RMVar_hsa_circ_267949,RMVar_hsa_circ_346675,RMVar_hsa_circ_70757,RMVar_hsa_circ_322827,RMVar_hsa_circ_159821,RMVar_hsa_circ_362077,RMVar_hsa_circ_57837,RMVar_hsa_circ_159822 27598 RMVar_ID_27598 Human_SNP_ID_515612632 A-to-I Human chr12 + 110328740 110328740 110328740 AGTGCATGCCACCATGCCCCACTAGTTTTTTTATTTTTTTTTGTAGAGGCAGGTTCTCACTATGT AGTGCATGCCACCATGCCCCACTAGTTTTTTTTTTTTTTTTTGTAGAGGCAGGTTCTCACTATGT A T ATP2A2 Ensembl:ENSG00000174437 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1173223626 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15765,RMVar_hsa_circ_159820,RMVar_hsa_circ_268494,RMVar_hsa_circ_101430,RMVar_hsa_circ_16970,RMVar_hsa_circ_267949,RMVar_hsa_circ_70757,RMVar_hsa_circ_159821,RMVar_hsa_circ_362077,RMVar_hsa_circ_57837,RMVar_hsa_circ_70026,RMVar_hsa_circ_277340,RMVar_hsa_circ_320646,RMVar_hsa_circ_373164,RMVar_hsa_circ_83406,RMVar_hsa_circ_159825,RMVar_hsa_circ_159826,RMVar_hsa_circ_159827,RMVar_hsa_circ_159824,RMVar_hsa_circ_30081 27599 RMVar_ID_27599 Human_SNP_ID_515612649 A-to-I Human chr12 + 110328802 110328802 110328802 TGTCACCAGGCTGGTCTTGAATTCCTGGGCTCAAGTGATCCTCCTGCCTTGGCCTCCCAAAGAGC TGTCACCAGGCTGGTCTTGAATTCCTGGGCTCGAGTGATCCTCCTGCCTTGGCCTCCCAAAGAGC A G ATP2A2 Ensembl:ENSG00000174437 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs956437650 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15765,RMVar_hsa_circ_159820,RMVar_hsa_circ_268494,RMVar_hsa_circ_101430,RMVar_hsa_circ_16970,RMVar_hsa_circ_267949,RMVar_hsa_circ_70757,RMVar_hsa_circ_159821,RMVar_hsa_circ_362077,RMVar_hsa_circ_57837,RMVar_hsa_circ_70026,RMVar_hsa_circ_277340,RMVar_hsa_circ_320646,RMVar_hsa_circ_373164,RMVar_hsa_circ_83406,RMVar_hsa_circ_159825,RMVar_hsa_circ_159826,RMVar_hsa_circ_159827,RMVar_hsa_circ_159824,RMVar_hsa_circ_30081 27600 RMVar_ID_27600 Human_SNP_ID_515612796 A-to-I Human chr12 + 110329494 110329494 110329494 GCTGTAGTGCAATGGCCCGATCTCAGCTCACTACAACCTCCGCCTTCTGGGTTCAAGCAATTCTC GCTGTAGTGCAATGGCCCGATCTCAGCTCACTGCAACCTCCGCCTTCTGGGTTCAAGCAATTCTC A G ATP2A2 Ensembl:ENSG00000174437 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1045490956 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15765,RMVar_hsa_circ_159820,RMVar_hsa_circ_268494,RMVar_hsa_circ_101430,RMVar_hsa_circ_16970,RMVar_hsa_circ_267949,RMVar_hsa_circ_70757,RMVar_hsa_circ_159821,RMVar_hsa_circ_362077,RMVar_hsa_circ_57837,RMVar_hsa_circ_70026,RMVar_hsa_circ_277340,RMVar_hsa_circ_320646,RMVar_hsa_circ_373164,RMVar_hsa_circ_83406,RMVar_hsa_circ_159825,RMVar_hsa_circ_159826,RMVar_hsa_circ_159827,RMVar_hsa_circ_159824,RMVar_hsa_circ_30081 27601 RMVar_ID_27601 Human_SNP_ID_515613158 A-to-I Human chr12 + 110331082 110331082 110331082 CCTGACTAACATGGTGAAACCTCGTCTCTACTAATATTACAAAAATTAGCTGGGCATGTTGGCAG CCTGACTAACATGGTGAAACCTCGTCTCTACTGATATTACAAAAATTAGCTGGGCATGTTGGCAG A G ATP2A2 Ensembl:ENSG00000174437 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs908968765 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15765,RMVar_hsa_circ_159820,RMVar_hsa_circ_268494,RMVar_hsa_circ_101430,RMVar_hsa_circ_16970,RMVar_hsa_circ_267949,RMVar_hsa_circ_70757,RMVar_hsa_circ_159821,RMVar_hsa_circ_362077,RMVar_hsa_circ_57837,RMVar_hsa_circ_70026,RMVar_hsa_circ_277340,RMVar_hsa_circ_320646,RMVar_hsa_circ_373164,RMVar_hsa_circ_83406,RMVar_hsa_circ_159825,RMVar_hsa_circ_159826,RMVar_hsa_circ_159827,RMVar_hsa_circ_159824,RMVar_hsa_circ_30081 27602 RMVar_ID_27602 Human_SNP_ID_515613183 A-to-I Human chr12 + 110331154 110331154 110331154 TAATTTCTTTGGGAGGCTGAGGCAGGAGAATCACTTGAACCCGGGAGGCGGAGGTTGCAGTGAGC TAATTTCTTTGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGGGAGGCGGAGGTTGCAGTGAGC A G ATP2A2 Ensembl:ENSG00000174437 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1416859468 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23305581 RMVar_hsa_circ_15765,RMVar_hsa_circ_159820,RMVar_hsa_circ_268494,RMVar_hsa_circ_101430,RMVar_hsa_circ_16970,RMVar_hsa_circ_267949,RMVar_hsa_circ_70757,RMVar_hsa_circ_159821,RMVar_hsa_circ_362077,RMVar_hsa_circ_57837,RMVar_hsa_circ_70026,RMVar_hsa_circ_277340,RMVar_hsa_circ_320646,RMVar_hsa_circ_373164,RMVar_hsa_circ_83406,RMVar_hsa_circ_159825,RMVar_hsa_circ_159826,RMVar_hsa_circ_159827,RMVar_hsa_circ_159824,RMVar_hsa_circ_30081 27603 RMVar_ID_27603 Human_SNP_ID_515613265 A-to-I Human chr12 + 110331481 110331481 110331481 TCTCCCTCAACCTCCTGAGTAGCTGGGATTACAGGTGCCCACCACCACGCCCGGCTAATTTGTTA TCTCCCTCAACCTCCTGAGTAGCTGGGATTACGGGTGCCCACCACCACGCCCGGCTAATTTGTTA A G ATP2A2 Ensembl:ENSG00000174437 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1331939483 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15765,RMVar_hsa_circ_159820,RMVar_hsa_circ_268494,RMVar_hsa_circ_101430,RMVar_hsa_circ_16970,RMVar_hsa_circ_267949,RMVar_hsa_circ_70757,RMVar_hsa_circ_159821,RMVar_hsa_circ_362077,RMVar_hsa_circ_57837,RMVar_hsa_circ_70026,RMVar_hsa_circ_277340,RMVar_hsa_circ_320646,RMVar_hsa_circ_373164,RMVar_hsa_circ_83406,RMVar_hsa_circ_159825,RMVar_hsa_circ_159826,RMVar_hsa_circ_159827,RMVar_hsa_circ_159824,RMVar_hsa_circ_30081 27604 RMVar_ID_27604 Human_SNP_ID_515618467 A-to-I Human chr12 + 110350881 110350881 110350881 TGCAGACAGCTATTTCGCACTGTATTAAATGTAACTTATTTAATGAAATCAGAAGCAGTAGACAG TGCAGACAGCTATTTCGCACTGTATTAAATGTGACTTATTTAATGAAATCAGAAGCAGTAGACAG A G ATP2A2 Ensembl:ENSG00000174437 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1226487844 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1463847,Human_RBP_ID_1786324,Human_RBP_ID_5554576,Human_RBP_ID_6129670,Human_RBP_ID_9010757,Human_RBP_ID_17467958,Human_RBP_ID_17600690,Human_RBP_ID_18255014,Human_RBP_ID_18617261,Human_RBP_ID_27622614 RMVar_hsa_circ_159820,RMVar_hsa_circ_101430,RMVar_hsa_circ_267949,RMVar_hsa_circ_100996,RMVar_hsa_circ_159835 27605 RMVar_ID_27605 Human_SNP_ID_515625878 A-to-I Human chr12 - 110378298 110378298 110378298 CCTGAGGTCAGGAGTTCGAGAGCAGCCTGACCAACATGGAGAAACCCCGTCTCTACTAAAAATAC CCTGAGGTCAGGAGTTCGAGAGCAGCCTGACCGACATGGAGAAACCCCGTCTCTACTAAAAATAC T C ANAPC7 Ensembl:ENSG00000196510 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs996117380 Functional Loss SNV dbSNP153 33..33 33 - - - 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 27606 RMVar_ID_27606 Human_SNP_ID_515626070 A-to-I Human chr12 - 110378991 110378991 110378991 AGCCAGGCATGGTGGTGCACGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATTGCT AGCCAGGCATGGTGGTGCACGCCTGTAGTCCCGGCTACTTGGGAGGCTGAGGCAGGAGAATTGCT T C ANAPC7 Ensembl:ENSG00000196510 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs962402447 Functional Loss SNV dbSNP153 33..33 33 - - - 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 27607 RMVar_ID_27607 Human_SNP_ID_515626095 A-to-I Human chr12 - 110379065 110379065 110379065 CTGACGTCAGGAGTTCGAGACCAGCCTAGCCAACATGGTGAACTACCATCTCTACTAAAAATAGA CTGACGTCAGGAGTTCGAGACCAGCCTAGCCAGCATGGTGAACTACCATCTCTACTAAAAATAGA T C ANAPC7 Ensembl:ENSG00000196510 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1248962436 Functional Loss SNV dbSNP153 33..33 33 - - - 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 27608 RMVar_ID_27608 Human_SNP_ID_515626096 A-to-I Human chr12 - 110379070 110379070 110379070 AACACCTGACGTCAGGAGTTCGAGACCAGCCTAGCCAACATGGTGAACTACCATCTCTACTAAAA AACACCTGACGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAACTACCATCTCTACTAAAA T C ANAPC7 Ensembl:ENSG00000196510 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1566260466 Functional Loss SNV dbSNP153 33..33 33 - - - 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 27609 RMVar_ID_27609 Human_SNP_ID_515626377 A-to-I Human chr12 - 110380299 110380299 110380299 TCACCCAGGCTGGAGTGCAGTGGTGCAATCTCAGCTCACTGCAACCTCCACTTGCCGGGTTTAAG TCACCCAGGCTGGAGTGCAGTGGTGCAATCTCGGCTCACTGCAACCTCCACTTGCCGGGTTTAAG T C ANAPC7 Ensembl:ENSG00000196510 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs201440638 Functional Loss SNV dbSNP153 33..33 33 - - - 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 27610 RMVar_ID_27610 Human_SNP_ID_515626387 A-to-I Human chr12 - 110380337 110380333 110380337 ATTTTTTTTATTTTTATTTGAGATAGAGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGTGCA ATTTTTTTTATTTTTATTTGAGATAGAGTCTC____TGTCACCCAGGCTGGAGTGCAGTGGTGCA AGAGT A ANAPC7 Ensembl:ENSG00000196510 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1226139005 Functional Loss DEL dbSNP153 33..36 33 - - - 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 27611 RMVar_ID_27611 Human_SNP_ID_515626391 A-to-I Human chr12 - 110380337 110380337 110380337 ATTTTTTTTATTTTTATTTGAGATAGAGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGTGCA ATTTTTTTTATTTTTATTTGAGATAGAGTCTCGCTCTGTCACCCAGGCTGGAGTGCAGTGGTGCA T C ANAPC7 Ensembl:ENSG00000196510 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1351029693 Functional Loss SNV dbSNP153 33..33 33 - - - 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 27612 RMVar_ID_27612 Human_SNP_ID_515626562 A-to-I Human chr12 - 110380822 110380822 110380822 GCCATTCTCCTGCCTCAGCCTCCCCAGTAGCTAGGATTACACCTGGCTAATTTTTTGTATTTTTA GCCATTCTCCTGCCTCAGCCTCCCCAGTAGCTGGGATTACACCTGGCTAATTTTTTGTATTTTTA T C ANAPC7 Ensembl:ENSG00000196510 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1397592879 Functional Loss SNV dbSNP153 33..33 33 - - - 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 27613 RMVar_ID_27613 Human_SNP_ID_515626570 A-to-I Human chr12 - 110380856 110380856 110380856 TCGGCTCACTGCAGGCTCCACCTCCCGGGTTAATGCCATTCTCCTGCCTCAGCCTCCCCAGTAGC TCGGCTCACTGCAGGCTCCACCTCCCGGGTTAGTGCCATTCTCCTGCCTCAGCCTCCCCAGTAGC T C ANAPC7 Ensembl:ENSG00000196510 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1424548340 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11805272,Human_RBP_ID_25018407 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 27614 RMVar_ID_27614 Human_SNP_ID_515626571 A-to-I Human chr12 - 110380857 110380857 110380857 CTCGGCTCACTGCAGGCTCCACCTCCCGGGTTAATGCCATTCTCCTGCCTCAGCCTCCCCAGTAG CTCGGCTCACTGCAGGCTCCACCTCCCGGGTTCATGCCATTCTCCTGCCTCAGCCTCCCCAGTAG T G ANAPC7 Ensembl:ENSG00000196510 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1191779171 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11805272,Human_RBP_ID_25018407 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 27615 RMVar_ID_27615 Human_SNP_ID_515626740 A-to-I Human chr12 - 110381405 110381405 110381405 TTGAACCTGGGAGGCGGAGGTTGCAGTGAGCCAAGATTGCGCCACTGCACTCCAGCCTGGCGACA TTGAACCTGGGAGGCGGAGGTTGCAGTGAGCCGAGATTGCGCCACTGCACTCCAGCCTGGCGACA T C ANAPC7 Ensembl:ENSG00000196510 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs969854922 Functional Loss SNV dbSNP153 33..33 33 - - - 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 27616 RMVar_ID_27616 Human_SNP_ID_515626756 A-to-I Human chr12 - 110381469 110381469 110381469 AGCTGGGCATGGTGGCTCACACCTGTAGTCCCAGCTACTTGGGAGGCTGAAGCAGGATAATCACT AGCTGGGCATGGTGGCTCACACCTGTAGTCCCGGCTACTTGGGAGGCTGAAGCAGGATAATCACT T C ANAPC7 Ensembl:ENSG00000196510 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1449720879 Functional Loss SNV dbSNP153 33..33 33 - - - 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 27617 RMVar_ID_27617 Human_SNP_ID_515628548 A-to-I Human chr12 - 110386985 110386985 110386985 GCTCAAGTGATTCTCCCACGTGGGCCTCCCAAAGTGCTGGGATTATAGACGTGAGCCACCATGCC GCTCAAGTGATTCTCCCACGTGGGCCTCCCAAGGTGCTGGGATTATAGACGTGAGCCACCATGCC T C ANAPC7 Ensembl:ENSG00000196510 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1024594190 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11805604 RMVar_hsa_circ_159849,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_159843,RMVar_hsa_circ_159848,RMVar_hsa_circ_341416,RMVar_hsa_circ_159841,RMVar_hsa_circ_271397,RMVar_hsa_circ_348929,RMVar_hsa_circ_308898 27618 RMVar_ID_27618 Human_SNP_ID_515629813 A-to-I Human chr12 - 110390369 110390369 110390369 TACTGTTGTGTTTAAAATCTACTAATTTTGCCAGACACGGTGGCTCACGCCTGTAATCCCAGCAC TACTGTTGTGTTTAAAATCTACTAATTTTGCCGGACACGGTGGCTCACGCCTGTAATCCCAGCAC T C AC144548.1,ANAPC7 Ensembl:ENSG00000258210,Ensembl:ENSG00000196510 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1029206702 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_159849,RMVar_hsa_circ_97652,RMVar_hsa_circ_159836,RMVar_hsa_circ_348195,RMVar_hsa_circ_32018,RMVar_hsa_circ_159839,RMVar_hsa_circ_282619,RMVar_hsa_circ_313132,RMVar_hsa_circ_159848,RMVar_hsa_circ_159841,RMVar_hsa_circ_271397,RMVar_hsa_circ_348929,RMVar_hsa_circ_308898,RMVar_hsa_circ_159851,RMVar_hsa_circ_283503,RMVar_hsa_circ_298432,RMVar_hsa_circ_159852,RMVar_hsa_circ_159854,RMVar_hsa_circ_370457,RMVar_hsa_circ_290931,RMVar_hsa_circ_159853 27619 RMVar_ID_27619 Human_SNP_ID_515631584 A-to-I Human chr12 - 110396649 110396649 110396649 AAAATTAGCTGGGTGTGGTGCCATGTGCCTGTAATCTCAGCTACTCGGGAGGCTGAGGAAGGAGA AAAATTAGCTGGGTGTGGTGCCATGTGCCTGTGATCTCAGCTACTCGGGAGGCTGAGGAAGGAGA T C AC144548.1,ANAPC7 Ensembl:ENSG00000258210,Ensembl:ENSG00000196510 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1482951419 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18617356 RMVar_hsa_circ_98968,RMVar_hsa_circ_159857 27620 RMVar_ID_27620 Human_SNP_ID_515631743 A-to-I Human chr12 - 110397117 110397117 110397117 TCGGCTCACTACAGGCCTCCTGGGTTCATGCCAGTCTCCTGCTTCAGCCTCCCAAGTAGCTGGGA TCGGCTCACTACAGGCCTCCTGGGTTCATGCCTGTCTCCTGCTTCAGCCTCCCAAGTAGCTGGGA T A AC144548.1,ANAPC7 Ensembl:ENSG00000258210,Ensembl:ENSG00000196510 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1349135271 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11806017 RMVar_hsa_circ_98968,RMVar_hsa_circ_159857 27621 RMVar_ID_27621 Human_SNP_ID_515631834 A-to-I Human chr12 - 110397472 110397472 110397472 CTCGGCTTACTATAACCTCCACCTCCTAGGTTAAAGCAATTCTCCTGCCTCAGCTTCCCGAGTAG CTCGGCTTACTATAACCTCCACCTCCTAGGTTGAAGCAATTCTCCTGCCTCAGCTTCCCGAGTAG T C AC144548.1,ANAPC7 Ensembl:ENSG00000258210,Ensembl:ENSG00000196510 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031280778 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11806039 RMVar_hsa_circ_98968,RMVar_hsa_circ_159857 27622 RMVar_ID_27622 Human_SNP_ID_515631841 A-to-I Human chr12 - 110397493 110397493 110397493 GTGCGAGTGCAGTGGCGCGATCTCGGCTTACTATAACCTCCACCTCCTAGGTTAAAGCAATTCTC GTGCGAGTGCAGTGGCGCGATCTCGGCTTACTGTAACCTCCACCTCCTAGGTTAAAGCAATTCTC T C AC144548.1,ANAPC7 Ensembl:ENSG00000258210,Ensembl:ENSG00000196510 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs550860567 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6130071,Human_RBP_ID_11806040 RMVar_hsa_circ_98968,RMVar_hsa_circ_159857 27623 RMVar_ID_27623 Human_SNP_ID_515632021 A-to-I Human chr12 - 110398049 110398049 110398049 TAGAGACGGGGTTTCACCTTATTGGCCAGGCTAGTCTCAAACTCCCAACCTTCAGTGATCTGCCT TAGAGACGGGGTTTCACCTTATTGGCCAGGCTTGTCTCAAACTCCCAACCTTCAGTGATCTGCCT T A AC144548.1,ANAPC7 Ensembl:ENSG00000258210,Ensembl:ENSG00000196510 lincRNA,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1176309626 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11806067,Human_RBP_ID_19716483 RMVar_hsa_circ_98968,RMVar_hsa_circ_159857 27624 RMVar_ID_27624 Human_SNP_ID_515632190 A-to-I Human chr12 - 110398796 110398796 110398796 GGATTACAGGCATGTGCCACCACGCCAGGCTAATTTTGTATTTTTAGTAGAGACAGGGTTTCTCC GGATTACAGGCATGTGCCACCACGCCAGGCTAGTTTTGTATTTTTAGTAGAGACAGGGTTTCTCC T C AC144548.1,ANAPC7 Ensembl:ENSG00000258210,Ensembl:ENSG00000196510 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs932163476 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11806123,Human_RBP_ID_24927976 RMVar_hsa_circ_98968,RMVar_hsa_circ_159857 27625 RMVar_ID_27625 Human_SNP_ID_515632292 A-to-I Human chr12 - 110399222 110399222 110399222 AGGTCAGGAGTTTGAGACCAGCGATGGCCAACATGGCGAAACCCCGTCTCTACCAAAAATACAAA AGGTCAGGAGTTTGAGACCAGCGATGGCCAACGTGGCGAAACCCCGTCTCTACCAAAAATACAAA T C AC144548.1,ANAPC7 Ensembl:ENSG00000258210,Ensembl:ENSG00000196510 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1382318862 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98968,RMVar_hsa_circ_159857 27626 RMVar_ID_27626 Human_SNP_ID_515632350 A-to-I Human chr12 - 110399403 110399403 110399403 AGACTCTAGGCTCAAGCAGTCTTCCCACCTCAACCTCCCAAAGTGTTGGGATTACAGGTGTGAGC AGACTCTAGGCTCAAGCAGTCTTCCCACCTCAGCCTCCCAAAGTGTTGGGATTACAGGTGTGAGC T C AC144548.1,ANAPC7 Ensembl:ENSG00000258210,Ensembl:ENSG00000196510 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1357729699 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5246482,Human_RBP_ID_11806150,Human_RBP_ID_17561266 RMVar_hsa_circ_98968,RMVar_hsa_circ_159857 27627 RMVar_ID_27627 Human_SNP_ID_515632437 A-to-I Human chr12 - 110399768 110399768 110399768 TTTTTTGTCTGAGACAGAGTCTCTCTCTCGTCACCCAGGCTGGAGTGCAGTGGTGGGATCTTGGC TTTTTTGTCTGAGACAGAGTCTCTCTCTCGTCGCCCAGGCTGGAGTGCAGTGGTGGGATCTTGGC T C AC144548.1,ANAPC7 Ensembl:ENSG00000258210,Ensembl:ENSG00000196510 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1280274489 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11806172,Human_RBP_ID_22898111,Human_RBP_ID_24927999 RMVar_hsa_circ_98968,RMVar_hsa_circ_159857 27628 RMVar_ID_27628 Human_SNP_ID_515632537 A-to-I Human chr12 - 110400028 110400028 110400028 GGAGTGCAGTGGCGTGATCTCGGCTCACTGCAACCTCCGCCTGCTGGGTTCAAGCAGTTCTCCCT GGAGTGCAGTGGCGTGATCTCGGCTCACTGCAGCCTCCGCCTGCTGGGTTCAAGCAGTTCTCCCT T C AC144548.1,ANAPC7 Ensembl:ENSG00000258210,Ensembl:ENSG00000196510 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444926431 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11806186 RMVar_hsa_circ_98968,RMVar_hsa_circ_159857 27629 RMVar_ID_27629 Human_SNP_ID_515633247 A-to-I Human chr12 - 110402427 110402427 110402427 TACTCGGGAGGCTGAGGCAGAAGAATAACGTGAACCCGGGAGGCGGAGCTTGCAGTGAGCCGAAG TACTCGGGAGGCTGAGGCAGAAGAATAACGTGTACCCGGGAGGCGGAGCTTGCAGTGAGCCGAAG T A AC144548.1,ANAPC7 Ensembl:ENSG00000258210,Ensembl:ENSG00000196510 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1431571011 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11806355 RMVar_hsa_circ_98968,RMVar_hsa_circ_159857 27630 RMVar_ID_27630 Human_SNP_ID_515633259 A-to-I Human chr12 - 110402468 110402468 110402468 AAATTTAGCCAGGCGTGGTGGCGGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGAAGA AAATTTAGCCAGGCGTGGTGGCGGGCGCCTGTGGTCCCAGCTACTCGGGAGGCTGAGGCAGAAGA T C AC144548.1,ANAPC7 Ensembl:ENSG00000258210,Ensembl:ENSG00000196510 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs925600750 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98968,RMVar_hsa_circ_159857 27631 RMVar_ID_27631 Human_SNP_ID_515642982 A-to-I Human chr12 - 110437403 110437403 110437403 AGATTGTGCCACTGCACTCCAGCCTGGGCAACAGAGCAAGACTCCGTCTCAAAAAAAAAAAGCAG AGATTGTGCCACTGCACTCCAGCCTGGGCAACGGAGCAAGACTCCGTCTCAAAAAAAAAAAGCAG T C AC144548.1,ARPC3 Ensembl:ENSG00000258210,Ensembl:ENSG00000111229 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1481083212 Functional Loss SNV dbSNP153 33..33 33 - - - 27632 RMVar_ID_27632 Human_SNP_ID_515643379 A-to-I Human chr12 - 110438893 110438893 110438893 CGCAGTGCCTCTGCCCGTAATTTGGGAGGCCAAGGCGGGCGGATCACCTGAGGTCGGGAGCTTGA CGCAGTGCCTCTGCCCGTAATTTGGGAGGCCAGGGCGGGCGGATCACCTGAGGTCGGGAGCTTGA T C AC144548.1,ARPC3 Ensembl:ENSG00000258210,Ensembl:ENSG00000111229 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs758722206 Functional Loss SNV dbSNP153 33..33 33 - - - 27633 RMVar_ID_27633 Human_SNP_ID_515643445 A-to-I Human chr12 - 110439123 110439123 110439123 AAATTAGCCAGGTGTAGTAGTGCATGCCTGTAATCCCAGCTACTCGGGAGGCTGAAGCACAAGAA AAATTAGCCAGGTGTAGTAGTGCATGCCTGTAGTCCCAGCTACTCGGGAGGCTGAAGCACAAGAA T C AC144548.1,ARPC3 Ensembl:ENSG00000258210,Ensembl:ENSG00000111229 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1057213148 Functional Loss SNV dbSNP153 33..33 33 - - - 27634 RMVar_ID_27634 Human_SNP_ID_515643452 A-to-I Human chr12 - 110439140 110439140 110439140 CTCTACCAAAAATACAAAAATTAGCCAGGTGTAGTAGTGCATGCCTGTAATCCCAGCTACTCGGG CTCTACCAAAAATACAAAAATTAGCCAGGTGTTGTAGTGCATGCCTGTAATCCCAGCTACTCGGG T A AC144548.1,ARPC3 Ensembl:ENSG00000258210,Ensembl:ENSG00000111229 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs553187950 Functional Loss SNV dbSNP153 33..33 33 - - - 27635 RMVar_ID_27635 Human_SNP_ID_515643468 A-to-I Human chr12 - 110439189 110439188 110439189 ATGATGCCAGGAGTTTGAGACCAGCCTGGCCAACAAAGCGAAACCCCATCTCTACCAAAAATACA ATGATGCCAGGAGTTTGAGACCAGCCTGGCCA_CAAAGCGAAACCCCATCTCTACCAAAAATACA GT G AC144548.1,ARPC3 Ensembl:ENSG00000258210,Ensembl:ENSG00000111229 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1265008518 Functional Loss DEL dbSNP153 33..33 33 - - - 27636 RMVar_ID_27636 Human_SNP_ID_515643483 A-to-I Human chr12 - 110439257 110439257 110439257 GAAAAATTAGTGCATGGTGGCTCACGCCTGTAATCCCAACACTTGGGAGGCTGAGGCGGGTGGAT GAAAAATTAGTGCATGGTGGCTCACGCCTGTAGTCCCAACACTTGGGAGGCTGAGGCGGGTGGAT T C AC144548.1,ARPC3 Ensembl:ENSG00000258210,Ensembl:ENSG00000111229 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1169214589 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5246548 27637 RMVar_ID_27637 Human_SNP_ID_515643578 A-to-I Human chr12 - 110439653 110439653 110439653 ATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACAATGTTAGGCAGGATGGTGTCTCGATCTCCT ATTTTTTGTATTTTTAGTAGAGACGGGGTTTCCCAATGTTAGGCAGGATGGTGTCTCGATCTCCT T G AC144548.1,ARPC3 Ensembl:ENSG00000258210,Ensembl:ENSG00000111229 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946041130 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5246554,Human_RBP_ID_24928128 27638 RMVar_ID_27638 Human_SNP_ID_515643596 A-to-I Human chr12 - 110439712 110439712 110439712 CTCCTGCCTCAGCCTCCCAGGTAGCTGGAACTACAGGCATGCACCACCACACCTGGCTAATTTTT CTCCTGCCTCAGCCTCCCAGGTAGCTGGAACTGCAGGCATGCACCACCACACCTGGCTAATTTTT T C AC144548.1,ARPC3 Ensembl:ENSG00000258210,Ensembl:ENSG00000111229 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs998382334 Functional Loss SNV dbSNP153 33..33 33 - - - 27639 RMVar_ID_27639 Human_SNP_ID_515643955 A-to-I Human chr12 - 110440983 110440983 110440983 AAAAATATAGCTGAGCATGGTGGCAGGTGCCTATAGCCCCAGCTACTTGGGAGGCTGAGGCAGGA AAAAATATAGCTGAGCATGGTGGCAGGTGCCTGTAGCCCCAGCTACTTGGGAGGCTGAGGCAGGA T C AC144548.1,ARPC3 Ensembl:ENSG00000258210,Ensembl:ENSG00000111229 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs566537530 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_357216 27640 RMVar_ID_27640 Human_SNP_ID_515644248 A-to-I Human chr12 - 110442026 110442026 110442026 CTAAAAAAAACTTTTTTTTTTTTTTTGGAGACAGAGTTTTGATCTCGTTGCCCAGGCTGGAGTGC CTAAAAAAAACTTTTTTTTTTTTTTTGGAGACGGAGTTTTGATCTCGTTGCCCAGGCTGGAGTGC T C AC144548.1,ARPC3 Ensembl:ENSG00000258210,Ensembl:ENSG00000111229 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10774601 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_357216 27641 RMVar_ID_27641 Human_SNP_ID_515644382 A-to-I Human chr12 - 110442521 110442521 110442521 TCACTGCAACCTCTGCCTCCTGGGTTCAAGCAATTCTCCTGCCTCAGCCCCCTGAGTAGCTGGGA TCACTGCAACCTCTGCCTCCTGGGTTCAAGCAGTTCTCCTGCCTCAGCCCCCTGAGTAGCTGGGA T C AC144548.1,ARPC3 Ensembl:ENSG00000258210,Ensembl:ENSG00000111229 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs952735508 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_357216 27642 RMVar_ID_27642 Human_SNP_ID_515644898 A-to-I Human chr12 - 110444564 110444564 110444564 AGAAAATCACAAGGCTGGGTGCGGTGGCTCACACTTGTAATCCCAGCACTTTGGAAGGCCAAGGC AGAAAATCACAAGGCTGGGTGCGGTGGCTCACTCTTGTAATCCCAGCACTTTGGAAGGCCAAGGC T A AC144548.1,ARPC3 Ensembl:ENSG00000258210,Ensembl:ENSG00000111229 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1211687292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3421384 RMVar_hsa_circ_357216 27643 RMVar_ID_27643 Human_SNP_ID_515645804 A-to-I Human chr12 - 110448079 110448076 110448079 GCCCAGGAGTTTGAGACCAACCTGGGCAACATAATGAGACCCTGCCTCTACAAAAATAAAAATAA GCCCAGGAGTTTGAGACCAACCTGGGCAACAT___GAGACCCTGCCTCTACAAAAATAAAAATAA CATT C ARPC3 Ensembl:ENSG00000111229 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs374662336 Functional Loss DEL dbSNP153 33..35 33 - - - 27644 RMVar_ID_27644 Human_SNP_ID_515646210 A-to-I Human chr12 - 110449502 110449502 110449502 GCTGGAGTGCAGTGAGGCGATCTCGGCTCACTACAACTTCCACCACCCTGGTTCAAGCAATTCTC GCTGGAGTGCAGTGAGGCGATCTCGGCTCACTGCAACTTCCACCACCCTGGTTCAAGCAATTCTC T C ARPC3 Ensembl:ENSG00000111229 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs527494347 Functional Loss SNV dbSNP153 33..33 33 - - - 27645 RMVar_ID_27645 Human_SNP_ID_515649018 A-to-I Human chr12 + 110460982 110460982 110460982 CAAGACTCCATCTCACTTTCCAACTTGGACCCAGCAGAATGGCTCCTGCAAAGAAGGGTGGCGAG CAAGACTCCATCTCACTTTCCAACTTGGACCCCGCAGAATGGCTCCTGCAAAGAAGGGTGGCGAG A C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs546708107 Functional Loss SNV dbSNP153 33..33 33 - - - 27646 RMVar_ID_27646 Human_SNP_ID_515649019 A-to-I Human chr12 + 110460982 110460982 110460982 CAAGACTCCATCTCACTTTCCAACTTGGACCCAGCAGAATGGCTCCTGCAAAGAAGGGTGGCGAG CAAGACTCCATCTCACTTTCCAACTTGGACCCGGCAGAATGGCTCCTGCAAAGAAGGGTGGCGAG A G - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs546708107 Functional Loss SNV dbSNP153 33..33 33 - - - 27647 RMVar_ID_27647 Human_SNP_ID_515649020 A-to-I Human chr12 + 110460982 110460982 110460982 CAAGACTCCATCTCACTTTCCAACTTGGACCCAGCAGAATGGCTCCTGCAAAGAAGGGTGGCGAG CAAGACTCCATCTCACTTTCCAACTTGGACCCTGCAGAATGGCTCCTGCAAAGAAGGGTGGCGAG A T - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs546708107 Functional Loss SNV dbSNP153 33..33 33 - - - 27648 RMVar_ID_27648 Human_SNP_ID_515649060 A-to-I Human chr12 + 110461118 110461118 110461118 CTATGGAGTGGGCTTCAAGAAGCGTGCCCCTCAGGCACTCAAAGAGATTCAGAAATTTGCCATGA CTATGGAGTGGGCTTCAAGAAGCGTGCCCCTCGGGCACTCAAAGAGATTCAGAAATTTGCCATGA A G RPL31P49 Ensembl:ENSG00000241680 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878920872 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1842503,Human_miRNA_ID_1855032,Human_miRNA_ID_1871477 27649 RMVar_ID_27649 Human_SNP_ID_515651326 A-to-I Human chr12 + 110469690 110469690 110469690 TGCCACCACGCCCGGCTAATTTTTGTATTTTTAGTAGAGAGGTGGTTTCACCATGTTGGCTAGGC TGCCACCACGCCCGGCTAATTTTTGTATTTTTGGTAGAGAGGTGGTTTCACCATGTTGGCTAGGC A G FAM216A Ensembl:ENSG00000204856 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs958948564 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11806808 RMVar_hsa_circ_159862,RMVar_hsa_circ_106783 27650 RMVar_ID_27650 Human_SNP_ID_515651327 A-to-I Human chr12 + 110469693 110469693 110469693 CACCACGCCCGGCTAATTTTTGTATTTTTAGTAGAGAGGTGGTTTCACCATGTTGGCTAGGCTTG CACCACGCCCGGCTAATTTTTGTATTTTTAGTGGAGAGGTGGTTTCACCATGTTGGCTAGGCTTG A G FAM216A Ensembl:ENSG00000204856 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991624658 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11806808 RMVar_hsa_circ_159862,RMVar_hsa_circ_106783 27651 RMVar_ID_27651 Human_SNP_ID_515651892 A-to-I Human chr12 + 110471976 110471976 110471976 TCTTTCGGCATGGCGTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGCGA TCTTTCGGCATGGCGTGGTGGCTCACACCTGTGATCCCAGCACTTTGGGAGGCTGAGGCGGGCGA A G FAM216A Ensembl:ENSG00000204856 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1267804249 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_159862,RMVar_hsa_circ_106783 27652 RMVar_ID_27652 Human_SNP_ID_515652023 A-to-I Human chr12 + 110472508 110472508 110472508 TTGAGCCCAGGATTTTGAGGCTGCGGTGGGCTATGATCACGACACTGCACTCTAGCCTGGGTGAA TTGAGCCCAGGATTTTGAGGCTGCGGTGGGCTGTGATCACGACACTGCACTCTAGCCTGGGTGAA A G FAM216A Ensembl:ENSG00000204856 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1328538819 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11806866 RMVar_hsa_circ_159862,RMVar_hsa_circ_106783 27653 RMVar_ID_27653 Human_SNP_ID_515654205 A-to-I Human chr12 + 110481444 110481444 110481444 TCAGCTCACTGCAACCTCTGCCTGCCAGGTTCAAGTGATTCTTCTGCCTCAGCCTCCCAAGTAGC TCAGCTCACTGCAACCTCTGCCTGCCAGGTTCGAGTGATTCTTCTGCCTCAGCCTCCCAAGTAGC A G FAM216A Ensembl:ENSG00000204856 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1191838956 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_159863,RMVar_hsa_circ_159862,RMVar_hsa_circ_106783,RMVar_hsa_circ_329080,RMVar_hsa_circ_344126,RMVar_hsa_circ_116293 27654 RMVar_ID_27654 Human_SNP_ID_515657305 A-to-I Human chr12 - 110493557 110493557 110493557 AGGAGTTTGAAACCAGCCTGGCCAACATGGTGAGACTCCGTCTCTACTAAAAATACAAAAAAATT AGGAGTTTGAAACCAGCCTGGCCAACATGGTGGGACTCCGTCTCTACTAAAAATACAAAAAAATT T C VPS29 Ensembl:ENSG00000111237 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs924119740 Functional Loss SNV dbSNP153 33..33 33 - - - 27655 RMVar_ID_27655 Human_SNP_ID_515657642 A-to-I Human chr12 - 110494941 110494941 110494941 CCTAGGTGGGTGGATCATGAGGTCAAGAGATCAAGACCATCCTGGCTGATACGGTGAAACCCCAT CCTAGGTGGGTGGATCATGAGGTCAAGAGATCGAGACCATCCTGGCTGATACGGTGAAACCCCAT T C VPS29 Ensembl:ENSG00000111237 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1181449186 Functional Loss SNV dbSNP153 33..33 33 - - - 27656 RMVar_ID_27656 Human_SNP_ID_515657787 A-to-I Human chr12 - 110495596 110495596 110495596 TTCAACCGATTCTCCTGCCTAACCTCCCAAGTAGCTGAGACTACAGGCACACACCATCACATCCA TTCAACCGATTCTCCTGCCTAACCTCCCAAGTTGCTGAGACTACAGGCACACACCATCACATCCA T A VPS29 Ensembl:ENSG00000111237 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs910332149 Functional Loss SNV dbSNP153 33..33 33 - - - 27657 RMVar_ID_27657 Human_SNP_ID_515658242 A-to-I Human chr12 - 110497463 110497463 110497463 CCTGTAATCCTAGCACTTTGGGAGGCGGAGGCAGGTGGATCACCTGAGGTCAGGAGTTCCAGACC CCTGTAATCCTAGCACTTTGGGAGGCGGAGGCGGGTGGATCACCTGAGGTCAGGAGTTCCAGACC T C VPS29 Ensembl:ENSG00000111237 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs184629901 Functional Loss SNV dbSNP153 33..33 33 - - - 27658 RMVar_ID_27658 Human_SNP_ID_515658285 A-to-I Human chr12 - 110497661 110497661 110497661 GTCTCGAACTCCTGACCTCAAGTATTCTGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGT GTCTCGAACTCCTGACCTCAAGTATTCTGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGT T C VPS29 Ensembl:ENSG00000111237 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1565862373 Functional Loss SNV dbSNP153 33..33 33 - - - 27659 RMVar_ID_27659 Human_SNP_ID_515658310 A-to-I Human chr12 - 110497773 110497773 110497773 CTGCCTCAACCTCCCAAGTTGGCTGGGATTACAGGCGCCTGCCACCGTGCCCAGCTAACTTTTGT CTGCCTCAACCTCCCAAGTTGGCTGGGATTACGGGCGCCTGCCACCGTGCCCAGCTAACTTTTGT T C VPS29 Ensembl:ENSG00000111237 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973224929 Functional Loss SNV dbSNP153 33..33 33 - - - 27660 RMVar_ID_27660 Human_SNP_ID_515658338 A-to-I Human chr12 - 110497904 110497904 110497904 TTTTTTGTTTGTTTGTTTTGAGACAGAGTCTCACTCTGCTGCCCAGGCTGGAGTGCCAGTGGCAT TTTTTTGTTTGTTTGTTTTGAGACAGAGTCTCCCTCTGCTGCCCAGGCTGGAGTGCCAGTGGCAT T G VPS29 Ensembl:ENSG00000111237 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900040951 Functional Loss SNV dbSNP153 33..33 33 - - - 27661 RMVar_ID_27661 Human_SNP_ID_515658372 A-to-I Human chr12 - 110497993 110497993 110497993 CACTCCAGCCTGGGCGACGAGAGCAAAATTCCATCTCAAAAAAAAAAAAAAAAAATCGATTCTGT CACTCCAGCCTGGGCGACGAGAGCAAAATTCCGTCTCAAAAAAAAAAAAAAAAAATCGATTCTGT T C VPS29 Ensembl:ENSG00000111237 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1461780122 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23155658,Human_RBP_ID_25018544 27662 RMVar_ID_27662 Human_SNP_ID_515669138 A-to-I Human chr12 - 110541556 110541556 110541556 AGCTGGGATTACAGGCGTGTGCCACCACGCCCAGCTAATTTTTTGTATTTTTGGTAGAAACGGGT AGCTGGGATTACAGGCGTGTGCCACCACGCCCGGCTAATTTTTTGTATTTTTGGTAGAAACGGGT T C PPTC7 Ensembl:ENSG00000196850 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1237609508 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45249,RMVar_hsa_circ_159877,RMVar_hsa_circ_159876,RMVar_hsa_circ_360322,RMVar_hsa_circ_159878,RMVar_hsa_circ_26501,RMVar_hsa_circ_338395 27663 RMVar_ID_27663 Human_SNP_ID_515669851 A-to-I Human chr12 - 110544181 110544181 110544181 AGTAAAAGTAACTTTTACCGGTAAAAGTCTAAATATTCTTCCAATTATGGTCACCAGTCTAAATC AGTAAAAGTAACTTTTACCGGTAAAAGTCTAATTATTCTTCCAATTATGGTCACCAGTCTAAATC T A PPTC7 Ensembl:ENSG00000196850 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041303637 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45249,RMVar_hsa_circ_159877,RMVar_hsa_circ_159876,RMVar_hsa_circ_360322,RMVar_hsa_circ_159878,RMVar_hsa_circ_26501,RMVar_hsa_circ_338395 27664 RMVar_ID_27664 Human_SNP_ID_515670109 A-to-I Human chr12 - 110545257 110545257 110545257 GAAACCCCATCTCTACTAAAAATGCAAAAATTAGCTGGGCGTGATGGCGGGCGCCTGTAGTCCCA GAAACCCCATCTCTACTAAAAATGCAAAAATTGGCTGGGCGTGATGGCGGGCGCCTGTAGTCCCA T C PPTC7 Ensembl:ENSG00000196850 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs551856926 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45249,RMVar_hsa_circ_159877,RMVar_hsa_circ_159876,RMVar_hsa_circ_360322,RMVar_hsa_circ_159878,RMVar_hsa_circ_26501,RMVar_hsa_circ_338395 27665 RMVar_ID_27665 Human_SNP_ID_515672183 A-to-I Human chr12 - 110553937 110553937 110553937 GAATCACTTGAACCTGGGAGGCAGAGGTTGCCATGAGCTGAGATCACGCCACTGTACTCCAGCAG GAATCACTTGAACCTGGGAGGCAGAGGTTGCCTTGAGCTGAGATCACGCCACTGTACTCCAGCAG T A PPTC7 Ensembl:ENSG00000196850 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1395691921 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98314,RMVar_hsa_circ_125433,RMVar_hsa_circ_159880,RMVar_hsa_circ_159881 27666 RMVar_ID_27666 Human_SNP_ID_515672184 A-to-I Human chr12 - 110553937 110553937 110553937 GAATCACTTGAACCTGGGAGGCAGAGGTTGCCATGAGCTGAGATCACGCCACTGTACTCCAGCAG GAATCACTTGAACCTGGGAGGCAGAGGTTGCCGTGAGCTGAGATCACGCCACTGTACTCCAGCAG T C PPTC7 Ensembl:ENSG00000196850 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1395691921 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98314,RMVar_hsa_circ_125433,RMVar_hsa_circ_159880,RMVar_hsa_circ_159881 27667 RMVar_ID_27667 Human_SNP_ID_515673404 A-to-I Human chr12 - 110559302 110559302 110559302 GTAGAAACCAGGCATGGTGATTTGTGCTTGTAATCCCAGCACTTTGGGAGACTGAGGCAGGAGGA GTAGAAACCAGGCATGGTGATTTGTGCTTGTAGTCCCAGCACTTTGGGAGACTGAGGCAGGAGGA T C PPTC7 Ensembl:ENSG00000196850 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1293317412 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98314,RMVar_hsa_circ_125433,RMVar_hsa_circ_159880,RMVar_hsa_circ_159881 27668 RMVar_ID_27668 Human_SNP_ID_515673676 A-to-I Human chr12 - 110560278 110560278 110560278 TCCCACCCTCAGCCTCCTGTTTAGCTGGAACTACAGGTGTGTGCCACCATCCCTGGCTGATTTTT TCCCACCCTCAGCCTCCTGTTTAGCTGGAACTGCAGGTGTGTGCCACCATCCCTGGCTGATTTTT T C PPTC7 Ensembl:ENSG00000196850 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs371396728 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98314,RMVar_hsa_circ_125433,RMVar_hsa_circ_159880,RMVar_hsa_circ_159881 27669 RMVar_ID_27669 Human_SNP_ID_515674297 A-to-I Human chr12 - 110562605 110562605 110562605 TATTTTTAGTAGAGATGAAGTTTCACCATGTTAGCCAGGCTGGTCTCAAACTCCTGACCTCAAGT TATTTTTAGTAGAGATGAAGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTCCTGACCTCAAGT T C PPTC7 Ensembl:ENSG00000196850 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1159455153 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98314,RMVar_hsa_circ_125433,RMVar_hsa_circ_159880,RMVar_hsa_circ_159881 27670 RMVar_ID_27670 Human_SNP_ID_515679185 A-to-I Human chr12 - 110580931 110580931 110580931 ACTGACCAATATGGTGAAACCCAGTCTTTACTAAAAATACAAAAATTAGCCGGGCGTGATGGCGC ACTGACCAATATGGTGAAACCCAGTCTTTACTGAAAATACAAAAATTAGCCGGGCGTGATGGCGC T C PPTC7 Ensembl:ENSG00000196850 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs767302729 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98314,RMVar_hsa_circ_125433,RMVar_hsa_circ_159880,RMVar_hsa_circ_159881 27671 RMVar_ID_27671 Human_SNP_ID_515679186 A-to-I Human chr12 - 110580931 110580931 110580931 ACTGACCAATATGGTGAAACCCAGTCTTTACTAAAAATACAAAAATTAGCCGGGCGTGATGGCGC ACTGACCAATATGGTGAAACCCAGTCTTTACTCAAAATACAAAAATTAGCCGGGCGTGATGGCGC T G PPTC7 Ensembl:ENSG00000196850 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs767302729 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98314,RMVar_hsa_circ_125433,RMVar_hsa_circ_159880,RMVar_hsa_circ_159881 27672 RMVar_ID_27672 Human_SNP_ID_515687403 A-to-I Human chr12 + 110615089 110615089 110615089 CAACTCGGGTGGATTGCTTGAGGTAGGAGTTCAAGATCAGTCTGGTCAAAATGGCGAAACCCAGT CAACTCGGGTGGATTGCTTGAGGTAGGAGTTCGAGATCAGTCTGGTCAAAATGGCGAAACCCAGT A G TCTN1 Ensembl:ENSG00000204852 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1303389863 Functional Loss SNV dbSNP153 33..33 33 - - - 27673 RMVar_ID_27673 Human_SNP_ID_515694054 A-to-I Human chr12 + 110643772 110643772 110643772 TCAGGCTCACTGCAGCCTTGGCCTACAGGCTCAAGCAATCCTCCTGCTTCAGCCTCCTAATAGCT TCAGGCTCACTGCAGCCTTGGCCTACAGGCTCCAGCAATCCTCCTGCTTCAGCCTCCTAATAGCT A C TCTN1 Ensembl:ENSG00000204852 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1437999338 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98052,RMVar_hsa_circ_159885 27674 RMVar_ID_27674 Human_SNP_ID_515694069 A-to-I Human chr12 + 110643844 110643844 110643844 CATGCGGGTACCATCACACCTGGCTAATTTTTAAAATTTTGGTAGAGACAGGGTCTCCCTTTGTT CATGCGGGTACCATCACACCTGGCTAATTTTTTAAATTTTGGTAGAGACAGGGTCTCCCTTTGTT A T TCTN1 Ensembl:ENSG00000204852 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs12305298 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98052,RMVar_hsa_circ_159885 27675 RMVar_ID_27675 Human_SNP_ID_515694081 A-to-I Human chr12 + 110643881 110643881 110643881 TTTGGTAGAGACAGGGTCTCCCTTTGTTTCCCAGGCTGGTCTCGAACTCCTGGGCTCAAGTGCTC TTTGGTAGAGACAGGGTCTCCCTTTGTTTCCCGGGCTGGTCTCGAACTCCTGGGCTCAAGTGCTC A G TCTN1 Ensembl:ENSG00000204852 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs757045070 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98052,RMVar_hsa_circ_159885 27676 RMVar_ID_27676 Human_SNP_ID_515694212 A-to-I Human chr12 + 110644593 110644593 110644593 CCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCTGGGAGGCGGTGGTTGCAGTGAGC CCAGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACCTGGGAGGCGGTGGTTGCAGTGAGC A G TCTN1 Ensembl:ENSG00000204852 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1566007385 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98052,RMVar_hsa_circ_159885 27677 RMVar_ID_27677 Human_SNP_ID_515696953 A-to-I Human chr12 - 110655797 110655797 110655797 GGGAGGCTGAAGTGGGAGAATTGCTTGAACTCAGGAGGCAGAGGTTGCAGTGAGGCGAGATCATG GGGAGGCTGAAGTGGGAGAATTGCTTGAACTCGGGAGGCAGAGGTTGCAGTGAGGCGAGATCATG T C HVCN1 Ensembl:ENSG00000122986 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1029124180 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116883,RMVar_hsa_circ_159894,RMVar_hsa_circ_159895 27678 RMVar_ID_27678 Human_SNP_ID_515699668 A-to-I Human chr12 - 110667466 110667466 110667466 GTGATCGCACACTACAGTCCAGCCTGGGTGACAGAGCGAGACCCTATCTCAAAAAAGGGAATTAT GTGATCGCACACTACAGTCCAGCCTGGGTGACCGAGCGAGACCCTATCTCAAAAAAGGGAATTAT T G HVCN1 Ensembl:ENSG00000122986 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs963574845 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116883,RMVar_hsa_circ_159895,RMVar_hsa_circ_367375 27679 RMVar_ID_27679 Human_SNP_ID_515699696 A-to-I Human chr12 - 110667578 110667578 110667578 AAAAATACAAAAAATTAGCTGAGCGTGATGGTATGTGCCTATAGTTCCAGCTACTCAGGAGGCTT AAAAATACAAAAAATTAGCTGAGCGTGATGGTGTGTGCCTATAGTTCCAGCTACTCAGGAGGCTT T C HVCN1 Ensembl:ENSG00000122986 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs977508300 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116883,RMVar_hsa_circ_159895,RMVar_hsa_circ_367375 27680 RMVar_ID_27680 Human_SNP_ID_515699857 A-to-I Human chr12 - 110668380 110668380 110668380 ATGCCTCAGCCTCCCAAGTAGCTGGGATTACAAGTGCCCACCACCACGCCTGGCTATTTTTTTGT ATGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGTGCCCACCACCACGCCTGGCTATTTTTTTGT T C HVCN1 Ensembl:ENSG00000122986 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7955616 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116883,RMVar_hsa_circ_159895,RMVar_hsa_circ_367375 27681 RMVar_ID_27681 Human_SNP_ID_515699859 A-to-I Human chr12 - 110668383 110668383 110668383 TTCATGCCTCAGCCTCCCAAGTAGCTGGGATTACAAGTGCCCACCACCACGCCTGGCTATTTTTT TTCATGCCTCAGCCTCCCAAGTAGCTGGGATTTCAAGTGCCCACCACCACGCCTGGCTATTTTTT T A HVCN1 Ensembl:ENSG00000122986 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1193738011 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116883,RMVar_hsa_circ_159895,RMVar_hsa_circ_367375 27682 RMVar_ID_27682 Human_SNP_ID_515699879 A-to-I Human chr12 - 110668497 110668497 110668497 TTTTGGGGTTTTTTGTTTTGTTTTCTTGAGACAGTCTCACTCTGTCACCCAGGCTGGAGTGCAGT TTTTGGGGTTTTTTGTTTTGTTTTCTTGAGACTGTCTCACTCTGTCACCCAGGCTGGAGTGCAGT T A HVCN1 Ensembl:ENSG00000122986 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs879217068 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116883,RMVar_hsa_circ_159895,RMVar_hsa_circ_367375 27683 RMVar_ID_27683 Human_SNP_ID_515702795 A-to-I Human chr12 - 110682055 110682055 110682055 TGAACTTGGGAGGCAGAGGTTGCAGTGAGCCAAGATCGCACCATTGCACTCCATCCTGGGTGACA TGAACTTGGGAGGCAGAGGTTGCAGTGAGCCAGGATCGCACCATTGCACTCCATCCTGGGTGACA T C HVCN1 Ensembl:ENSG00000122986 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1041799360 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116883,RMVar_hsa_circ_159895,RMVar_hsa_circ_367375 27684 RMVar_ID_27684 Human_SNP_ID_515702807 A-to-I Human chr12 - 110682112 110682112 110682112 ATCCTGACACACACCTCTAATCCCAGCTGCTTAGGAGGATAAGGCAGGAGAATCGCTTGAACTTG ATCCTGACACACACCTCTAATCCCAGCTGCTTGGGAGGATAAGGCAGGAGAATCGCTTGAACTTG T C HVCN1 Ensembl:ENSG00000122986 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1000332917 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116883,RMVar_hsa_circ_159895,RMVar_hsa_circ_367375 27685 RMVar_ID_27685 Human_SNP_ID_515710098 A-to-I Human chr12 - 110712557 110712557 110712557 TGGCTCAGTGCAACCTCCGCTTCCCGGATTCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTACCT TGGCTCAGTGCAACCTCCGCTTCCCGGATTCAGGTGATTCTCCTGCCTCAGCCTCCCGAGTACCT T C lnc-HVCN1-2 RNACentral:URS00008BF997 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1169036635 Functional Loss SNV dbSNP153 33..33 33 - - - 27686 RMVar_ID_27686 Human_SNP_ID_515711454 A-to-I Human chr12 - 110717518 110717518 110717518 ATGGTGATGGGCGCATGTAGTCCCAGTTACTCAGGAGCCTGAGGCAGGAGAATGGCGTGAACCTG ATGGTGATGGGCGCATGTAGTCCCAGTTACTCGGGAGCCTGAGGCAGGAGAATGGCGTGAACCTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1304024171 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11808232 27687 RMVar_ID_27687 Human_SNP_ID_515713915 A-to-I Human chr12 - 110727062 110727062 110727062 GTGGTGGTGCACACCTGTAGTCGCGGACACTCAGGAGATTGAGGCAGGAAAATCACTGGAACCTG GTGGTGGTGCACACCTGTAGTCGCGGACACTCGGGAGATTGAGGCAGGAAAATCACTGGAACCTG T C PPP1CC Ensembl:ENSG00000186298 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1361904871 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11808488 RMVar_hsa_circ_109554,RMVar_hsa_circ_113906,RMVar_hsa_circ_82370,RMVar_hsa_circ_159900,RMVar_hsa_circ_159902,RMVar_hsa_circ_159901,RMVar_hsa_circ_366726,RMVar_hsa_circ_88206,RMVar_hsa_circ_159905,RMVar_hsa_circ_159903,RMVar_hsa_circ_318389 27688 RMVar_ID_27688 Human_SNP_ID_515889914 A-to-I Human chr12 - 111461401 111461401 111461401 CAATGGTGTGATGTCGGTTCACTGCAACCTCCACCTCCCGGGTTCAAGCTATTCTCCTTCCCCAC CAATGGTGTGATGTCGGTTCACTGCAACCTCCGCCTCCCGGGTTCAAGCTATTCTCCTTCCCCAC T C ATXN2 Ensembl:ENSG00000204842 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1378518723 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73316,RMVar_hsa_circ_95149,RMVar_hsa_circ_266965,RMVar_hsa_circ_127347,RMVar_hsa_circ_159939,RMVar_hsa_circ_355663,RMVar_hsa_circ_104595,RMVar_hsa_circ_106949,RMVar_hsa_circ_88500,RMVar_hsa_circ_159941,RMVar_hsa_circ_159943,RMVar_hsa_circ_159944,RMVar_hsa_circ_159942,RMVar_hsa_circ_159945,RMVar_hsa_circ_374827,RMVar_hsa_circ_159940,RMVar_hsa_circ_358772 27689 RMVar_ID_27689 Human_SNP_ID_515889915 A-to-I Human chr12 - 111461407 111461407 111461407 GGAGTGCAATGGTGTGATGTCGGTTCACTGCAACCTCCACCTCCCGGGTTCAAGCTATTCTCCTT GGAGTGCAATGGTGTGATGTCGGTTCACTGCATCCTCCACCTCCCGGGTTCAAGCTATTCTCCTT T A ATXN2 Ensembl:ENSG00000204842 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1406333256 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11811684 RMVar_hsa_circ_73316,RMVar_hsa_circ_95149,RMVar_hsa_circ_266965,RMVar_hsa_circ_127347,RMVar_hsa_circ_159939,RMVar_hsa_circ_355663,RMVar_hsa_circ_104595,RMVar_hsa_circ_106949,RMVar_hsa_circ_88500,RMVar_hsa_circ_159941,RMVar_hsa_circ_159943,RMVar_hsa_circ_159944,RMVar_hsa_circ_159942,RMVar_hsa_circ_159945,RMVar_hsa_circ_374827,RMVar_hsa_circ_159940,RMVar_hsa_circ_358772 27690 RMVar_ID_27690 Human_SNP_ID_515891030 A-to-I Human chr12 - 111465515 111465515 111465515 TGTCTGCCTAGGCCTCCCAAAGTGCTGGGATTACAGATGTGAGCCACCACGCCCAGCCTCACATC TGTCTGCCTAGGCCTCCCAAAGTGCTGGGATTGCAGATGTGAGCCACCACGCCCAGCCTCACATC T C ATXN2 Ensembl:ENSG00000204842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs563448896 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24929456 RMVar_hsa_circ_127332,RMVar_hsa_circ_95149,RMVar_hsa_circ_127347,RMVar_hsa_circ_159939,RMVar_hsa_circ_355663,RMVar_hsa_circ_104595,RMVar_hsa_circ_106949,RMVar_hsa_circ_88500,RMVar_hsa_circ_159941,RMVar_hsa_circ_159943,RMVar_hsa_circ_159944,RMVar_hsa_circ_159942,RMVar_hsa_circ_159940,RMVar_hsa_circ_358772,RMVar_hsa_circ_321842,RMVar_hsa_circ_70282,RMVar_hsa_circ_71324,RMVar_hsa_circ_159946 27691 RMVar_ID_27691 Human_SNP_ID_515891103 A-to-I Human chr12 - 111465738 111465738 111465738 TTTGAGGTAGTCTCACTCTGTCACCCATTCTGAAGTGCAGCGGTGCGATCTCAGCTCACTGCAAC TTTGAGGTAGTCTCACTCTGTCACCCATTCTGGAGTGCAGCGGTGCGATCTCAGCTCACTGCAAC T C ATXN2 Ensembl:ENSG00000204842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1378149432 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6132100,Human_RBP_ID_23155688 RMVar_hsa_circ_127332,RMVar_hsa_circ_95149,RMVar_hsa_circ_127347,RMVar_hsa_circ_159939,RMVar_hsa_circ_355663,RMVar_hsa_circ_104595,RMVar_hsa_circ_106949,RMVar_hsa_circ_88500,RMVar_hsa_circ_159941,RMVar_hsa_circ_159943,RMVar_hsa_circ_159944,RMVar_hsa_circ_159942,RMVar_hsa_circ_159940,RMVar_hsa_circ_358772,RMVar_hsa_circ_321842,RMVar_hsa_circ_70282,RMVar_hsa_circ_71324,RMVar_hsa_circ_159946 27692 RMVar_ID_27692 Human_SNP_ID_515891933 A-to-I Human chr12 - 111468786 111468786 111468786 TGAGGCAACAGAATTGCTTGAACCCGGGAGGCAGAGGTTGCAGTGAGCCGAGATCGCGCCACTAC TGAGGCAACAGAATTGCTTGAACCCGGGAGGCGGAGGTTGCAGTGAGCCGAGATCGCGCCACTAC T C ATXN2 Ensembl:ENSG00000204842 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1309406435 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127332,RMVar_hsa_circ_95149,RMVar_hsa_circ_127347,RMVar_hsa_circ_159939,RMVar_hsa_circ_355663,RMVar_hsa_circ_104595,RMVar_hsa_circ_106949,RMVar_hsa_circ_88500,RMVar_hsa_circ_159941,RMVar_hsa_circ_159943,RMVar_hsa_circ_159944,RMVar_hsa_circ_159942,RMVar_hsa_circ_159940,RMVar_hsa_circ_358772,RMVar_hsa_circ_321842,RMVar_hsa_circ_70282,RMVar_hsa_circ_71324,RMVar_hsa_circ_159946 27693 RMVar_ID_27693 Human_SNP_ID_515892985 A-to-I Human chr12 - 111473055 111473055 111473055 TTGCCCAGGCTGGTGTCGAACTCCTGAGCTCAAGCAGTCTGCCTGTGTCAGCCTCACAAAGTGGT TTGCCCAGGCTGGTGTCGAACTCCTGAGCTCAGGCAGTCTGCCTGTGTCAGCCTCACAAAGTGGT T C ATXN2 Ensembl:ENSG00000204842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs927366094 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63893,RMVar_hsa_circ_127332,RMVar_hsa_circ_95149,RMVar_hsa_circ_127347,RMVar_hsa_circ_159939,RMVar_hsa_circ_104595,RMVar_hsa_circ_106949,RMVar_hsa_circ_88500,RMVar_hsa_circ_159941,RMVar_hsa_circ_159943,RMVar_hsa_circ_159944,RMVar_hsa_circ_159942,RMVar_hsa_circ_112342,RMVar_hsa_circ_346982,RMVar_hsa_circ_70282,RMVar_hsa_circ_71324,RMVar_hsa_circ_369472,RMVar_hsa_circ_159946,RMVar_hsa_circ_369910,RMVar_hsa_circ_348253,RMVar_hsa_circ_329294,RMVar_hsa_circ_287456,RMVar_hsa_circ_159948,RMVar_hsa_circ_159950,RMVar_hsa_circ_36744,RMVar_hsa_circ_159951,RMVar_hsa_circ_159949,RMVar_hsa_circ_159947 27694 RMVar_ID_27694 Human_SNP_ID_515893341 A-to-I Human chr12 - 111474521 111474521 111474521 AGCTCACTGCTGCTGCGAATTCCTGGTCTCAAAGGATCCTCCCTCCTCAGCCTCTCAAGTAACTG AGCTCACTGCTGCTGCGAATTCCTGGTCTCAAGGGATCCTCCCTCCTCAGCCTCTCAAGTAACTG T C ATXN2 Ensembl:ENSG00000204842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1461644059 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63893,RMVar_hsa_circ_127332,RMVar_hsa_circ_95149,RMVar_hsa_circ_127347,RMVar_hsa_circ_159939,RMVar_hsa_circ_104595,RMVar_hsa_circ_106949,RMVar_hsa_circ_88500,RMVar_hsa_circ_159941,RMVar_hsa_circ_159943,RMVar_hsa_circ_159944,RMVar_hsa_circ_159942,RMVar_hsa_circ_112342,RMVar_hsa_circ_346982,RMVar_hsa_circ_70282,RMVar_hsa_circ_71324,RMVar_hsa_circ_369472,RMVar_hsa_circ_159946,RMVar_hsa_circ_369910,RMVar_hsa_circ_348253,RMVar_hsa_circ_329294,RMVar_hsa_circ_287456,RMVar_hsa_circ_159948,RMVar_hsa_circ_159950,RMVar_hsa_circ_36744,RMVar_hsa_circ_159951,RMVar_hsa_circ_159949,RMVar_hsa_circ_159947 27695 RMVar_ID_27695 Human_SNP_ID_515898243 A-to-I Human chr12 - 111493856 111493856 111493856 TGGAAGGCAAAGGTGGGGCGAATCACAAGGTTAGGAGTTCGAGACCAGCCTGACCAACGTGGTGA TGGAAGGCAAAGGTGGGGCGAATCACAAGGTTGGGAGTTCGAGACCAGCCTGACCAACGTGGTGA T C ATXN2 Ensembl:ENSG00000204842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335021186 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23527,RMVar_hsa_circ_127332,RMVar_hsa_circ_106949,RMVar_hsa_circ_159944,RMVar_hsa_circ_112342,RMVar_hsa_circ_346982,RMVar_hsa_circ_71324,RMVar_hsa_circ_369472,RMVar_hsa_circ_159946,RMVar_hsa_circ_287456,RMVar_hsa_circ_159948,RMVar_hsa_circ_159949,RMVar_hsa_circ_159947,RMVar_hsa_circ_69228,RMVar_hsa_circ_324608,RMVar_hsa_circ_367516,RMVar_hsa_circ_289901,RMVar_hsa_circ_35923,RMVar_hsa_circ_42990,RMVar_hsa_circ_159956,RMVar_hsa_circ_285995,RMVar_hsa_circ_358393,RMVar_hsa_circ_373818,RMVar_hsa_circ_378187,RMVar_hsa_circ_371084,RMVar_hsa_circ_331285,RMVar_hsa_circ_105452,RMVar_hsa_circ_264967,RMVar_hsa_circ_95165,RMVar_hsa_circ_159958,RMVar_hsa_circ_159962,RMVar_hsa_circ_79660,RMVar_hsa_circ_159963,RMVar_hsa_circ_159960,RMVar_hsa_circ_159961,RMVar_hsa_circ_159959,RMVar_hsa_circ_159957,RMVar_hsa_circ_351079,RMVar_hsa_circ_58327,RMVar_hsa_circ_347569,RMVar_hsa_circ_159970 27696 RMVar_ID_27696 Human_SNP_ID_515910738 A-to-I Human chr12 - 111544071 111544071 111544071 AAATTAATTTTTTTTCTTTTTTTTAAAGAAACAGGGTCATGCTCTGTCACTCAGGCTGGAATGCA AAATTAATTTTTTTTCTTTTTTTTAAAGAAACGGGGTCATGCTCTGTCACTCAGGCTGGAATGCA T C ATXN2 Ensembl:ENSG00000204842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1321053109 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11813160 RMVar_hsa_circ_23527,RMVar_hsa_circ_106949,RMVar_hsa_circ_159944,RMVar_hsa_circ_369472,RMVar_hsa_circ_159947,RMVar_hsa_circ_324608,RMVar_hsa_circ_35923,RMVar_hsa_circ_378187,RMVar_hsa_circ_264967,RMVar_hsa_circ_79660,RMVar_hsa_circ_159957,RMVar_hsa_circ_20030,RMVar_hsa_circ_57216,RMVar_hsa_circ_302926,RMVar_hsa_circ_325318,RMVar_hsa_circ_159976,RMVar_hsa_circ_112869,RMVar_hsa_circ_159978,RMVar_hsa_circ_159977,RMVar_hsa_circ_271823,RMVar_hsa_circ_105608,RMVar_hsa_circ_159984,RMVar_hsa_circ_159985,RMVar_hsa_circ_159986,RMVar_hsa_circ_12154,RMVar_hsa_circ_56014,RMVar_hsa_circ_361924,RMVar_hsa_circ_348698,RMVar_hsa_circ_40069,RMVar_hsa_circ_66727,RMVar_hsa_circ_159988,RMVar_hsa_circ_299732,RMVar_hsa_circ_53715,RMVar_hsa_circ_293747,RMVar_hsa_circ_282991,RMVar_hsa_circ_159990,RMVar_hsa_circ_159991 27697 RMVar_ID_27697 Human_SNP_ID_515914272 A-to-I Human chr12 - 111558775 111558775 111558775 AATTATTTTTTGAGACAGGGTTTTGCTCTGTCACCAATGCTGGAGTGCAGTGGCATAATCACAGC AATTATTTTTTGAGACAGGGTTTTGCTCTGTCGCCAATGCTGGAGTGCAGTGGCATAATCACAGC T C ATXN2 Ensembl:ENSG00000204842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978610162 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_159986,RMVar_hsa_circ_124044,RMVar_hsa_circ_159993,RMVar_hsa_circ_159992 27698 RMVar_ID_27698 Human_SNP_ID_515918595 A-to-I Human chr12 - 111574642 111574642 111574642 AAGGGAGGAGGGTCGCTTGAGCTCAGGAATTCAAGATCAGCCTAGGCAACATAGTGAGGCCCCAT AAGGGAGGAGGGTCGCTTGAGCTCAGGAATTCCAGATCAGCCTAGGCAACATAGTGAGGCCCCAT T G ATXN2 Ensembl:ENSG00000204842 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1020751979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17561272,Human_RBP_ID_25018738 RMVar_hsa_circ_124044,RMVar_hsa_circ_159992 27699 RMVar_ID_27699 Human_SNP_ID_515919174 A-to-I Human chr12 - 111576608 111576608 111576608 TGTGCGTGGCTCATCTACAGTCTCAGTGACTCAGAAGGCTGAGGCAGGAGAATCTCTTGAACCCG TGTGCGTGGCTCATCTACAGTCTCAGTGACTCGGAAGGCTGAGGCAGGAGAATCTCTTGAACCCG T C ATXN2 Ensembl:ENSG00000204842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1395083333 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124044,RMVar_hsa_circ_159992 27700 RMVar_ID_27700 Human_SNP_ID_515919175 A-to-I Human chr12 - 111576608 111576608 111576608 TGTGCGTGGCTCATCTACAGTCTCAGTGACTCAGAAGGCTGAGGCAGGAGAATCTCTTGAACCCG TGTGCGTGGCTCATCTACAGTCTCAGTGACTCCGAAGGCTGAGGCAGGAGAATCTCTTGAACCCG T G ATXN2 Ensembl:ENSG00000204842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1395083333 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124044,RMVar_hsa_circ_159992 27701 RMVar_ID_27701 Human_SNP_ID_515919851 A-to-I Human chr12 - 111578938 111578938 111578938 GACCTCCTGGGCTCAAGTGATCCTCCTGCCTCAGCCTCCTGGCTGGGACCACAGGCATGTACCAC GACCTCCTGGGCTCAAGTGATCCTCCTGCCTCGGCCTCCTGGCTGGGACCACAGGCATGTACCAC T C ATXN2 Ensembl:ENSG00000204842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913056764 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2304666,Human_RBP_ID_11814204 RMVar_hsa_circ_124044,RMVar_hsa_circ_159992 27702 RMVar_ID_27702 Human_SNP_ID_515920275 A-to-I Human chr12 - 111580497 111580497 111580497 TCTTTTTTTTTTTTTTCTTTTTTGGAGACAGAATCTTCCTCTGTTGCTCAGGGTGGAGTGTAGTG TCTTTTTTTTTTTTTTCTTTTTTGGAGACAGACTCTTCCTCTGTTGCTCAGGGTGGAGTGTAGTG T G ATXN2 Ensembl:ENSG00000204842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1418233040 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2304674,Human_RBP_ID_6132754,Human_RBP_ID_18935675 RMVar_hsa_circ_124044,RMVar_hsa_circ_159992 27703 RMVar_ID_27703 Human_SNP_ID_515920776 A-to-I Human chr12 - 111582116 111582116 111582116 TTACCCGGGCTGGTTTTGAACTTCTGCCCTCAAGTACTCCTCTTGCCTTGGCCTCCCAAAGTATT TTACCCGGGCTGGTTTTGAACTTCTGCCCTCAGGTACTCCTCTTGCCTTGGCCTCCCAAAGTATT T C ATXN2 Ensembl:ENSG00000204842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1225745704 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11814334 RMVar_hsa_circ_124044,RMVar_hsa_circ_159992 27704 RMVar_ID_27704 Human_SNP_ID_515920900 A-to-I Human chr12 - 111582513 111582513 111582513 GCCTTTAACTCCTGGGTTCAAGTGATCCTCCCACCTCAGCCTCCTGAGTAGCTGGGACCACAGGC GCCTTTAACTCCTGGGTTCAAGTGATCCTCCCGCCTCAGCCTCCTGAGTAGCTGGGACCACAGGC T C ATXN2 Ensembl:ENSG00000204842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215014655 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124044,RMVar_hsa_circ_159992 27705 RMVar_ID_27705 Human_SNP_ID_515921842 A-to-I Human chr12 - 111585474 111585474 111585474 GAATCTTGTTCTGTTGCCCAGGCTGGAGTGCAATGGTACAATCTTGGCCCACTGCAACCTCTGCC GAATCTTGTTCTGTTGCCCAGGCTGGAGTGCAGTGGTACAATCTTGGCCCACTGCAACCTCTGCC T C ATXN2 Ensembl:ENSG00000204842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1033792343 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11814457 RMVar_hsa_circ_124044,RMVar_hsa_circ_159992 27706 RMVar_ID_27706 Human_SNP_ID_515921862 A-to-I Human chr12 - 111585548 111585548 111585548 CGCCTGCTTCAGCCTCCCAAAGTGCCGGGACCACAGGCGTGAGCCACCGCACCTGGCTTTTTTTT CGCCTGCTTCAGCCTCCCAAAGTGCCGGGACCGCAGGCGTGAGCCACCGCACCTGGCTTTTTTTT T C ATXN2 Ensembl:ENSG00000204842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs966740330 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24930387 RMVar_hsa_circ_124044,RMVar_hsa_circ_159992 27707 RMVar_ID_27707 Human_SNP_ID_515922034 A-to-I Human chr12 - 111585995 111585995 111585995 CTACTTGGGAGGCTGAGGCAGGTGGTTCACTTAAGTCTGGATGTCGAGGTGAGCCATGATTGCAC CTACTTGGGAGGCTGAGGCAGGTGGTTCACTTGAGTCTGGATGTCGAGGTGAGCCATGATTGCAC T C ATXN2 Ensembl:ENSG00000204842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs912383551 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11814480,Human_RBP_ID_17561278 RMVar_hsa_circ_124044,RMVar_hsa_circ_159992 27708 RMVar_ID_27708 Human_SNP_ID_515937211 A-to-I Human chr12 - 111643487 111643487 111643487 AGCTCCACTGTTTATTTTTGGTGACTTCGTACATCATTATGAACCGCAATTAAGGAGGAGGCTTA AGCTCCACTGTTTATTTTTGGTGACTTCGTACGTCATTATGAACCGCAATTAAGGAGGAGGCTTA T C BRAP Ensembl:ENSG00000089234 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6416335 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2797,GWAS_ID_2798 RMVar_hsa_circ_88385,RMVar_hsa_circ_159997 27709 RMVar_ID_27709 Human_SNP_ID_515941892 A-to-I Human chr12 - 111661788 111661788 111661788 AGAATCATTTGAACCTGGGTGGCAGAGGCTGCAGTGAGCTGAGATCGCGCCACTGCACTCTAGCC AGAATCATTTGAACCTGGGTGGCAGAGGCTGCGGTGAGCTGAGATCGCGCCACTGCACTCTAGCC T C BRAP Ensembl:ENSG00000089234 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1301069391 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44170,RMVar_hsa_circ_88385,RMVar_hsa_circ_298392,RMVar_hsa_circ_159997,RMVar_hsa_circ_336533,RMVar_hsa_circ_360733,RMVar_hsa_circ_70565,RMVar_hsa_circ_160001,RMVar_hsa_circ_282740,RMVar_hsa_circ_54046,RMVar_hsa_circ_126381,RMVar_hsa_circ_160002,RMVar_hsa_circ_273842,RMVar_hsa_circ_290110,RMVar_hsa_circ_310817,RMVar_hsa_circ_160006,RMVar_hsa_circ_160007,RMVar_hsa_circ_160008,RMVar_hsa_circ_94855,RMVar_hsa_circ_105112,RMVar_hsa_circ_160009,RMVar_hsa_circ_265321,RMVar_hsa_circ_160010 27710 RMVar_ID_27710 Human_SNP_ID_515941902 A-to-I Human chr12 - 111661849 111661849 111661849 AAATTAGCTGGGCATGGGGGTGCATGCCTACAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAA AAATTAGCTGGGCATGGGGGTGCATGCCTACAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAA T C BRAP Ensembl:ENSG00000089234 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042259648 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44170,RMVar_hsa_circ_88385,RMVar_hsa_circ_298392,RMVar_hsa_circ_159997,RMVar_hsa_circ_336533,RMVar_hsa_circ_360733,RMVar_hsa_circ_70565,RMVar_hsa_circ_160001,RMVar_hsa_circ_282740,RMVar_hsa_circ_54046,RMVar_hsa_circ_126381,RMVar_hsa_circ_160002,RMVar_hsa_circ_273842,RMVar_hsa_circ_290110,RMVar_hsa_circ_310817,RMVar_hsa_circ_160006,RMVar_hsa_circ_160007,RMVar_hsa_circ_160008,RMVar_hsa_circ_94855,RMVar_hsa_circ_105112,RMVar_hsa_circ_160009,RMVar_hsa_circ_265321,RMVar_hsa_circ_160010 27711 RMVar_ID_27711 Human_SNP_ID_515944283 A-to-I Human chr12 - 111671783 111671783 111671783 TACTCAGGACCCTGAAGCAGGAAGATCACCTGAGTCGGGGGAGGTCCAGGCTATAGTGAGCCGTG TACTCAGGACCCTGAAGCAGGAAGATCACCTGCGTCGGGGGAGGTCCAGGCTATAGTGAGCCGTG T G BRAP Ensembl:ENSG00000089234 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs566276147 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44170,RMVar_hsa_circ_88385,RMVar_hsa_circ_298392,RMVar_hsa_circ_159997,RMVar_hsa_circ_360733,RMVar_hsa_circ_70565,RMVar_hsa_circ_160001,RMVar_hsa_circ_282740,RMVar_hsa_circ_54046,RMVar_hsa_circ_126381,RMVar_hsa_circ_160002,RMVar_hsa_circ_273842,RMVar_hsa_circ_290110,RMVar_hsa_circ_160006,RMVar_hsa_circ_160007,RMVar_hsa_circ_160008,RMVar_hsa_circ_105112,RMVar_hsa_circ_160009,RMVar_hsa_circ_265321,RMVar_hsa_circ_160012,RMVar_hsa_circ_318185,RMVar_hsa_circ_332217,RMVar_hsa_circ_284737,RMVar_hsa_circ_160011 27712 RMVar_ID_27712 Human_SNP_ID_515944370 A-to-I Human chr12 - 111672084 111672084 111672084 TGCTAGCCTCAGCCTCCTGGGTAGCTGGGACTACAAGTGTGTACCACCACGCCTGGCTAATTTTT TGCTAGCCTCAGCCTCCTGGGTAGCTGGGACTGCAAGTGTGTACCACCACGCCTGGCTAATTTTT T C BRAP Ensembl:ENSG00000089234 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs530793477 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44170,RMVar_hsa_circ_88385,RMVar_hsa_circ_298392,RMVar_hsa_circ_159997,RMVar_hsa_circ_360733,RMVar_hsa_circ_70565,RMVar_hsa_circ_160001,RMVar_hsa_circ_282740,RMVar_hsa_circ_54046,RMVar_hsa_circ_126381,RMVar_hsa_circ_160002,RMVar_hsa_circ_273842,RMVar_hsa_circ_290110,RMVar_hsa_circ_160006,RMVar_hsa_circ_160007,RMVar_hsa_circ_160008,RMVar_hsa_circ_105112,RMVar_hsa_circ_160009,RMVar_hsa_circ_265321,RMVar_hsa_circ_160012,RMVar_hsa_circ_318185,RMVar_hsa_circ_332217,RMVar_hsa_circ_284737,RMVar_hsa_circ_160011 27713 RMVar_ID_27713 Human_SNP_ID_515948392 A-to-I Human chr12 + 111686670 111686670 111686670 CCCGGGAGGCGGAGGTTGCAGTGAGTCGAGATAGTGCTAGTGCACTCCCGCCTGGGCAACAAGAG CCCGGGAGGCGGAGGTTGCAGTGAGTCGAGATGGTGCTAGTGCACTCCCGCCTGGGCAACAAGAG A G ACAD10 Ensembl:ENSG00000111271 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs796396321 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87833,RMVar_hsa_circ_160020 27714 RMVar_ID_27714 Human_SNP_ID_515949121 A-to-I Human chr12 + 111689576 111689576 111689576 TTTCTGTGTTTTTAGTAGAGACGGGGCTTCACAATGTTGACCAGGTTGGTCTCGAACTCTCGACC TTTCTGTGTTTTTAGTAGAGACGGGGCTTCACGATGTTGACCAGGTTGGTCTCGAACTCTCGACC A G ACAD10 Ensembl:ENSG00000111271 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1441802598 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87833,RMVar_hsa_circ_160020 27715 RMVar_ID_27715 Human_SNP_ID_515949366 A-to-I Human chr12 + 111690523 111690523 111690523 TTTTTTAGTCCTAGCTGGGCGCCGTGACTCACACCTGTAATTCCAGCACTTTGGGAGGCTGAGGT TTTTTTAGTCCTAGCTGGGCGCCGTGACTCACGCCTGTAATTCCAGCACTTTGGGAGGCTGAGGT A G ACAD10 Ensembl:ENSG00000111271 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs771494113 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1425620,Human_Splice_Rec_1425621 RMVar_hsa_circ_87833,RMVar_hsa_circ_160020 27716 RMVar_ID_27716 Human_SNP_ID_515951482 A-to-I Human chr12 + 111698928 111698928 111698928 TTGAAACGGAATTTTACTCTGCCACTCAGGCTAAAGTGCAGTGGAGTGACCTCGGCTCACTGCAA TTGAAACGGAATTTTACTCTGCCACTCAGGCTGAAGTGCAGTGGAGTGACCTCGGCTCACTGCAA A G ACAD10 Ensembl:ENSG00000111271 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1267546083 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14163,RMVar_hsa_circ_87833,RMVar_hsa_circ_290146,RMVar_hsa_circ_296193,RMVar_hsa_circ_317305,RMVar_hsa_circ_160020,RMVar_hsa_circ_319884,RMVar_hsa_circ_308726,RMVar_hsa_circ_47982,RMVar_hsa_circ_55381,RMVar_hsa_circ_26611,RMVar_hsa_circ_160022,RMVar_hsa_circ_160023 27717 RMVar_ID_27717 Human_SNP_ID_515956570 A-to-I Human chr12 + 111718982 111718982 111718982 CAAAAGTAAGCCAAGTGTGGTGGTGCACACCTATAGTCCCAGCCAATCTCGAGGCTGAGGCAGGA CAAAAGTAAGCCAAGTGTGGTGGTGCACACCTGTAGTCCCAGCCAATCTCGAGGCTGAGGCAGGA A G ACAD10 Ensembl:ENSG00000111271 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs571658586 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15642,RMVar_hsa_circ_87833,RMVar_hsa_circ_296193,RMVar_hsa_circ_317305,RMVar_hsa_circ_160020,RMVar_hsa_circ_319884,RMVar_hsa_circ_308726,RMVar_hsa_circ_55381,RMVar_hsa_circ_67355,RMVar_hsa_circ_52958,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_28348,RMVar_hsa_circ_304780,RMVar_hsa_circ_313083,RMVar_hsa_circ_304077,RMVar_hsa_circ_160027,RMVar_hsa_circ_160028 27718 RMVar_ID_27718 Human_SNP_ID_515958580 A-to-I Human chr12 + 111725252 111725252 111725252 GACATTGACCGGGCATAGTGGCTCACTCCTGTAATCCCAGCACTTAAGGAGGCTGAGGCAGGTAG GACATTGACCGGGCATAGTGGCTCACTCCTGTCATCCCAGCACTTAAGGAGGCTGAGGCAGGTAG A C ACAD10 Ensembl:ENSG00000111271 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs930191021 Functional Loss SNV dbSNP153 33..33 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 27719 RMVar_ID_27719 Human_SNP_ID_515960621 A-to-I Human chr12 + 111733215 111733215 111733215 CCAACTCCTGGGCTCAGTGATGCTCCCACCTTAGCCTCCTGAGTAGCTGGGACTACAGGCGTGCA CCAACTCCTGGGCTCAGTGATGCTCCCACCTTCGCCTCCTGAGTAGCTGGGACTACAGGCGTGCA A C ACAD10 Ensembl:ENSG00000111271 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1245780874 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87833,RMVar_hsa_circ_296193,RMVar_hsa_circ_160020,RMVar_hsa_circ_308726,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_88262,RMVar_hsa_circ_160027,RMVar_hsa_circ_340070,RMVar_hsa_circ_160030,RMVar_hsa_circ_160035,RMVar_hsa_circ_160033,RMVar_hsa_circ_335017,RMVar_hsa_circ_336003,RMVar_hsa_circ_160032,RMVar_hsa_circ_121488,RMVar_hsa_circ_273225,RMVar_hsa_circ_160034 27720 RMVar_ID_27720 Human_SNP_ID_515964025 A-to-I Human chr12 + 111746527 111746527 111746527 CTCCTGCCTCAGCTTCCCAAGTAGCTGGGACTACAGGCATGTGCCACCACACCTGGCTAATTTTT CTCCTGCCTCAGCTTCCCAAGTAGCTGGGACTGCAGGCATGTGCCACCACACCTGGCTAATTTTT A G ACAD10 Ensembl:ENSG00000111271 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1192666193 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44534,RMVar_hsa_circ_70361,RMVar_hsa_circ_90316,RMVar_hsa_circ_160038 27721 RMVar_ID_27721 Human_SNP_ID_515964089 A-to-I Human chr12 + 111746814 111746814 111746814 CTTGAGGCCAGGAGTTCGACACCAGCGTGTGCAACATAGAACTCTGTATGTACAAAAAAATAAAA CTTGAGGCCAGGAGTTCGACACCAGCGTGTGCCACATAGAACTCTGTATGTACAAAAAAATAAAA A C ACAD10 Ensembl:ENSG00000111271 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs377345645 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17560921 RMVar_hsa_circ_44534,RMVar_hsa_circ_70361,RMVar_hsa_circ_90316,RMVar_hsa_circ_160038 27722 RMVar_ID_27722 Human_SNP_ID_515964104 A-to-I Human chr12 + 111746877 111746877 111746877 AAAATTAATCGGGTGTGATGGTGCATACCTGTAGTCTCAGCTGCTTGGGAAGCTGAGGCATGGGA AAAATTAATCGGGTGTGATGGTGCATACCTGTGGTCTCAGCTGCTTGGGAAGCTGAGGCATGGGA A G ACAD10 Ensembl:ENSG00000111271 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs776574825 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44534,RMVar_hsa_circ_70361,RMVar_hsa_circ_90316,RMVar_hsa_circ_160038 27723 RMVar_ID_27723 Human_SNP_ID_515965170 A-to-I Human chr12 + 111750452 111750452 111750452 AAAAAGAAAAAGTTTTAAGTGCCAGGCATGGTAGCATGTGTCTCTAGTCCCAGCTACTCAGGAGG AAAAAGAAAAAGTTTTAAGTGCCAGGCATGGTCGCATGTGTCTCTAGTCCCAGCTACTCAGGAGG A C ACAD10 Ensembl:ENSG00000111271 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1463552251 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44534,RMVar_hsa_circ_118560,RMVar_hsa_circ_90316,RMVar_hsa_circ_160038,RMVar_hsa_circ_160039 27724 RMVar_ID_27724 Human_SNP_ID_515965784 A-to-I Human chr12 + 111753001 111753001 111753001 CCCTGTCTCTACAAAAAATTGGAAAGTTAGCTAGATGTGGTGGTTCTTGCCTGTGGTCCCAGCTA CCCTGTCTCTACAAAAAATTGGAAAGTTAGCTGGATGTGGTGGTTCTTGCCTGTGGTCCCAGCTA A G ACAD10 Ensembl:ENSG00000111271 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs888638621 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44534,RMVar_hsa_circ_118560,RMVar_hsa_circ_90316,RMVar_hsa_circ_160038,RMVar_hsa_circ_160039 27725 RMVar_ID_27725 Human_SNP_ID_515999188 A-to-I Human chr12 + 111891233 111891233 111891233 CTCCCACCCCAGCCTCCCAAGGAACTGGGACTACAGGCACGTACCACCATGCCCAGCTAATTTTT CTCCCACCCCAGCCTCCCAAGGAACTGGGACTGCAGGCACGTACCACCATGCCCAGCTAATTTTT A G MAPKAPK5 Ensembl:ENSG00000089022 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs952810075 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_160065 27726 RMVar_ID_27726 Human_SNP_ID_515999893 A-to-I Human chr12 + 111894104 111894104 111894104 TGCTCTTATCACCCAGGGTGGAGTGCAGTGGCACGATCTCGGCTCACTGCAACCTCTGTCTCCCA TGCTCTTATCACCCAGGGTGGAGTGCAGTGGCGCGATCTCGGCTCACTGCAACCTCTGTCTCCCA A G MAPKAPK5 Ensembl:ENSG00000089022 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs997270834 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11816857,Human_RBP_ID_17809462 27727 RMVar_ID_27727 Human_SNP_ID_516000395 A-to-I Human chr12 + 111895776 111895776 111895776 TGGTCTCAAACTCCTGACCTCGTGATCCGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGC TGGTCTCAAACTCCTGACCTCGTGATCCGCCCCCCTCGGCCTCCCAAAGTGCTGGGATTACAGGC A C MAPKAPK5 Ensembl:ENSG00000089022 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1275416284 Functional Loss SNV dbSNP153 33..33 33 - - - 27728 RMVar_ID_27728 Human_SNP_ID_516009480 A-to-I Human chr12 - 111933058 111933058 111933058 TTTTGTATTTTTAATAGAGACAGGGTTTCGCCATGTTGGCCAGGCTGGTCTCAACCTCCTGACCT TTTTGTATTTTTAATAGAGACAGGGTTTCGCCGTGTTGGCCAGGCTGGTCTCAACCTCCTGACCT T C TMEM116 Ensembl:ENSG00000198270 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs756737911 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_160067,RMVar_hsa_circ_160068,RMVar_hsa_circ_160072,RMVar_hsa_circ_100434,RMVar_hsa_circ_160069,RMVar_hsa_circ_160070,RMVar_hsa_circ_288508,RMVar_hsa_circ_293964,RMVar_hsa_circ_299054,RMVar_hsa_circ_266501,RMVar_hsa_circ_160074,RMVar_hsa_circ_160075,RMVar_hsa_circ_160073,RMVar_hsa_circ_160071 27729 RMVar_ID_27729 Human_SNP_ID_516009839 A-to-I Human chr12 - 111934576 111934576 111934576 TTTTTGTATTTTTAGTAGACACAGGTTTCACCATGCTGGTCAGGCTGTCTTGAACTCCTGACCTC TTTTTGTATTTTTAGTAGACACAGGTTTCACCTTGCTGGTCAGGCTGTCTTGAACTCCTGACCTC T A TMEM116 Ensembl:ENSG00000198270 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs532857202 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_160068,RMVar_hsa_circ_160072,RMVar_hsa_circ_100434,RMVar_hsa_circ_160069,RMVar_hsa_circ_160070,RMVar_hsa_circ_288508,RMVar_hsa_circ_293964,RMVar_hsa_circ_299054,RMVar_hsa_circ_266501,RMVar_hsa_circ_160074,RMVar_hsa_circ_160075,RMVar_hsa_circ_160073,RMVar_hsa_circ_160077,RMVar_hsa_circ_160079,RMVar_hsa_circ_289584,RMVar_hsa_circ_160071,RMVar_hsa_circ_296398,RMVar_hsa_circ_276015,RMVar_hsa_circ_160078,RMVar_hsa_circ_160076 27730 RMVar_ID_27730 Human_SNP_ID_516009876 A-to-I Human chr12 - 111934718 111934718 111934718 GTGTCTCGGTCTGTTGCCCAGGCTGGAGTGCAATGGCGCATCTCAGCTCACTACAACCTCTGCCT GTGTCTCGGTCTGTTGCCCAGGCTGGAGTGCAGTGGCGCATCTCAGCTCACTACAACCTCTGCCT T C TMEM116 Ensembl:ENSG00000198270 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049423464 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_160068,RMVar_hsa_circ_160072,RMVar_hsa_circ_100434,RMVar_hsa_circ_160069,RMVar_hsa_circ_160070,RMVar_hsa_circ_288508,RMVar_hsa_circ_293964,RMVar_hsa_circ_299054,RMVar_hsa_circ_266501,RMVar_hsa_circ_160074,RMVar_hsa_circ_160075,RMVar_hsa_circ_160073,RMVar_hsa_circ_160077,RMVar_hsa_circ_160079,RMVar_hsa_circ_289584,RMVar_hsa_circ_160071,RMVar_hsa_circ_296398,RMVar_hsa_circ_276015,RMVar_hsa_circ_160078,RMVar_hsa_circ_160076 27731 RMVar_ID_27731 Human_SNP_ID_516010131 A-to-I Human chr12 - 111935844 111935844 111935844 TTGAGGCCAGGAATTCGAAACTAGTCTGGCCAACATGGCTAAACCCCGTCTCTACTAAAAATACA TTGAGGCCAGGAATTCGAAACTAGTCTGGCCAGCATGGCTAAACCCCGTCTCTACTAAAAATACA T C TMEM116 Ensembl:ENSG00000198270 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs970693700 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_160068,RMVar_hsa_circ_160072,RMVar_hsa_circ_100434,RMVar_hsa_circ_160069,RMVar_hsa_circ_160070,RMVar_hsa_circ_288508,RMVar_hsa_circ_293964,RMVar_hsa_circ_299054,RMVar_hsa_circ_266501,RMVar_hsa_circ_160074,RMVar_hsa_circ_160075,RMVar_hsa_circ_160073,RMVar_hsa_circ_160077,RMVar_hsa_circ_160079,RMVar_hsa_circ_289584,RMVar_hsa_circ_160071,RMVar_hsa_circ_296398,RMVar_hsa_circ_276015,RMVar_hsa_circ_160078,RMVar_hsa_circ_160076 27732 RMVar_ID_27732 Human_SNP_ID_516023310 A-to-I Human chr12 - 111993800 111993800 111993800 AATCATCAGGGTGAGAAACAATTGCACAAAACACTCCAGGTATGTAACCTGCTACAAATGTTACA AATCATCAGGGTGAGAAACAATTGCACAAAACGCTCCAGGTATGTAACCTGCTACAAATGTTACA T C TMEM116 Ensembl:ENSG00000198270 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs534370328 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100434,RMVar_hsa_circ_266501,RMVar_hsa_circ_160071,RMVar_hsa_circ_331154,RMVar_hsa_circ_353788,RMVar_hsa_circ_31087,RMVar_hsa_circ_324713,RMVar_hsa_circ_377882 27733 RMVar_ID_27733 Human_SNP_ID_516023311 A-to-I Human chr12 - 111993800 111993800 111993800 AATCATCAGGGTGAGAAACAATTGCACAAAACACTCCAGGTATGTAACCTGCTACAAATGTTACA AATCATCAGGGTGAGAAACAATTGCACAAAACCCTCCAGGTATGTAACCTGCTACAAATGTTACA T G TMEM116 Ensembl:ENSG00000198270 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs534370328 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100434,RMVar_hsa_circ_266501,RMVar_hsa_circ_160071,RMVar_hsa_circ_331154,RMVar_hsa_circ_353788,RMVar_hsa_circ_31087,RMVar_hsa_circ_324713,RMVar_hsa_circ_377882 27734 RMVar_ID_27734 Human_SNP_ID_516023343 A-to-I Human chr12 - 111993926 111993923 111993927 GTGCAGTCAGAGTACCAGTCATAATGATACAGACAAACATTCCCTTCCATACACCTTTAAATCCA GTGCAGTCAGAGTACCAGTCATAATGATACA____AACATTCCCTTCCATACACCTTTAAATCCA TTGTC T TMEM116 Ensembl:ENSG00000198270 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1445385612 Functional Loss DEL dbSNP153 32..35 33 - - - RMVar_hsa_circ_100434,RMVar_hsa_circ_266501,RMVar_hsa_circ_160071,RMVar_hsa_circ_331154,RMVar_hsa_circ_353788,RMVar_hsa_circ_31087,RMVar_hsa_circ_324713,RMVar_hsa_circ_377882 27735 RMVar_ID_27735 Human_SNP_ID_516023344 A-to-I Human chr12 - 111993926 111993926 111993926 GTGCAGTCAGAGTACCAGTCATAATGATACAGACAAACATTCCCTTCCATACACCTTTAAATCCA GTGCAGTCAGAGTACCAGTCATAATGATACAGGCAAACATTCCCTTCCATACACCTTTAAATCCA T C TMEM116 Ensembl:ENSG00000198270 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879231952 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100434,RMVar_hsa_circ_266501,RMVar_hsa_circ_160071,RMVar_hsa_circ_331154,RMVar_hsa_circ_353788,RMVar_hsa_circ_31087,RMVar_hsa_circ_324713,RMVar_hsa_circ_377882 27736 RMVar_ID_27736 Human_SNP_ID_516023346 A-to-I Human chr12 - 111993928 111993928 111993928 TAGTGCAGTCAGAGTACCAGTCATAATGATACAGACAAACATTCCCTTCCATACACCTTTAAATC TAGTGCAGTCAGAGTACCAGTCATAATGATACGGACAAACATTCCCTTCCATACACCTTTAAATC T C TMEM116 Ensembl:ENSG00000198270 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs902369200 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100434,RMVar_hsa_circ_266501,RMVar_hsa_circ_160071,RMVar_hsa_circ_331154,RMVar_hsa_circ_353788,RMVar_hsa_circ_31087,RMVar_hsa_circ_324713,RMVar_hsa_circ_377882 27737 RMVar_ID_27737 Human_SNP_ID_516023350 A-to-I Human chr12 - 111993936 111993936 111993936 AACTACTGTAGTGCAGTCAGAGTACCAGTCATAATGATACAGACAAACATTCCCTTCCATACACC AACTACTGTAGTGCAGTCAGAGTACCAGTCATGATGATACAGACAAACATTCCCTTCCATACACC T C TMEM116 Ensembl:ENSG00000198270 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879001902 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100434,RMVar_hsa_circ_266501,RMVar_hsa_circ_160071,RMVar_hsa_circ_331154,RMVar_hsa_circ_353788,RMVar_hsa_circ_31087,RMVar_hsa_circ_324713,RMVar_hsa_circ_377882 27738 RMVar_ID_27738 Human_SNP_ID_516028822 A-to-I Human chr12 + 112016744 112016744 112016744 AACCCTGTCTCTACTAAAAATACAAAAAAATTAGCCGGACGTGGTGGCGGGCACCTGTAGTCCCA AACCCTGTCTCTACTAAAAATACAAAAAAATTCGCCGGACGTGGTGGCGGGCACCTGTAGTCCCA A C ERP29 Ensembl:ENSG00000089248 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs756706309 Functional Loss SNV dbSNP153 33..33 33 - - - 27739 RMVar_ID_27739 Human_SNP_ID_516029166 A-to-I Human chr12 + 112018243 112018243 112018243 TCATAGCTCACTATAACCTCTAACTCCTAGGCACAAGTGATTTTCCACCTCAGCCTCCTGAGTAG TCATAGCTCACTATAACCTCTAACTCCTAGGCGCAAGTGATTTTCCACCTCAGCCTCCTGAGTAG A G ERP29 Ensembl:ENSG00000089248 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs776106468 Functional Loss SNV dbSNP153 33..33 33 - - - 27740 RMVar_ID_27740 Human_SNP_ID_516029167 A-to-I Human chr12 + 112018243 112018243 112018243 TCATAGCTCACTATAACCTCTAACTCCTAGGCACAAGTGATTTTCCACCTCAGCCTCCTGAGTAG TCATAGCTCACTATAACCTCTAACTCCTAGGCTCAAGTGATTTTCCACCTCAGCCTCCTGAGTAG A T ERP29 Ensembl:ENSG00000089248 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs776106468 Functional Loss SNV dbSNP153 33..33 33 - - - 27741 RMVar_ID_27741 Human_SNP_ID_516029207 A-to-I Human chr12 + 112018398 112018397 112018399 AGCCTCACGTGATCCTCCCACTTCAGCCCCGCAAAGTGTTGAGATTACAGGTGTGAGCCACCATG AGCCTCACGTGATCCTCCCACTTCAGCCCCGC__AGTGTTGAGATTACAGGTGTGAGCCACCATG CAA C ERP29 Ensembl:ENSG00000089248 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1216809525 Functional Loss DEL dbSNP153 33..34 33 - - - 27742 RMVar_ID_27742 Human_SNP_ID_516029207 A-to-I Human chr12 + 112018399 112018397 112018399 GCCTCACGTGATCCTCCCACTTCAGCCCCGCAAAGTGTTGAGATTACAGGTGTGAGCCACCATGC GCCTCACGTGATCCTCCCACTTCAGCCCCGC__AGTGTTGAGATTACAGGTGTGAGCCACCATGC CAA C ERP29 Ensembl:ENSG00000089248 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1216809525 Functional Loss DEL dbSNP153 32..33 33 - - - 27743 RMVar_ID_27743 Human_SNP_ID_516033347 A-to-I Human chr12 - 112035777 112035777 112035777 GCTACTCAGGAGGCTGAAGCAGGAGGATCACCAGAGCCTGGGAAATTGAGGCTGCCGTGAGCTGT GCTACTCAGGAGGCTGAAGCAGGAGGATCACCGGAGCCTGGGAAATTGAGGCTGCCGTGAGCTGT T C NAA25 Ensembl:ENSG00000111300 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1204862299 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11817885 RMVar_hsa_circ_64741,RMVar_hsa_circ_72139,RMVar_hsa_circ_354048,RMVar_hsa_circ_378810,RMVar_hsa_circ_299492,RMVar_hsa_circ_65557,RMVar_hsa_circ_70220,RMVar_hsa_circ_65058,RMVar_hsa_circ_160089,RMVar_hsa_circ_20845 27744 RMVar_ID_27744 Human_SNP_ID_516033551 A-to-I Human chr12 - 112036788 112036788 112036788 TGCCCAGGCTGGAGTGCAATGGCGCAATCACTACAACCTCCACTTTCCAGTTTCAAGCGATTCTC TGCCCAGGCTGGAGTGCAATGGCGCAATCACTGCAACCTCCACTTTCCAGTTTCAAGCGATTCTC T C NAA25 Ensembl:ENSG00000111300 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs866453439 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17809569 RMVar_hsa_circ_64741,RMVar_hsa_circ_72139,RMVar_hsa_circ_354048,RMVar_hsa_circ_378810,RMVar_hsa_circ_299492,RMVar_hsa_circ_65557,RMVar_hsa_circ_70220,RMVar_hsa_circ_65058,RMVar_hsa_circ_160089,RMVar_hsa_circ_20845 27745 RMVar_ID_27745 Human_SNP_ID_516033929 A-to-I Human chr12 - 112038103 112038103 112038103 AGACTGAGGTATGAGAATTGCTTGAACCCGAGAGGCAGAGGTTGCAGTGAGCCAAGATAGCACCA AGACTGAGGTATGAGAATTGCTTGAACCCGAGTGGCAGAGGTTGCAGTGAGCCAAGATAGCACCA T A NAA25 Ensembl:ENSG00000111300 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1488692403 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64741,RMVar_hsa_circ_72139,RMVar_hsa_circ_354048,RMVar_hsa_circ_378810,RMVar_hsa_circ_299492,RMVar_hsa_circ_65557,RMVar_hsa_circ_70220,RMVar_hsa_circ_65058,RMVar_hsa_circ_160089,RMVar_hsa_circ_20845 27746 RMVar_ID_27746 Human_SNP_ID_516040000 A-to-I Human chr12 - 112064395 112064395 112064395 AAAACCCCGTGTCTACTAAAAATACAAAAATTAGCCAGGTGTGGTGGTGCATGCCTGTACTGTAG AAAACCCCGTGTCTACTAAAAATACAAAAATTGGCCAGGTGTGGTGGTGCATGCCTGTACTGTAG T C NAA25 Ensembl:ENSG00000111300 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs774797931 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24931761 RMVar_hsa_circ_64741,RMVar_hsa_circ_65557,RMVar_hsa_circ_36254,RMVar_hsa_circ_61015,RMVar_hsa_circ_44174,RMVar_hsa_circ_160095,RMVar_hsa_circ_62757,RMVar_hsa_circ_36025,RMVar_hsa_circ_337661,RMVar_hsa_circ_30457,RMVar_hsa_circ_160100,RMVar_hsa_circ_160099,RMVar_hsa_circ_110973,RMVar_hsa_circ_348874,RMVar_hsa_circ_349132,RMVar_hsa_circ_356087,RMVar_hsa_circ_347978,RMVar_hsa_circ_287779,RMVar_hsa_circ_160101,RMVar_hsa_circ_160102,RMVar_hsa_circ_160103 27747 RMVar_ID_27747 Human_SNP_ID_516040143 A-to-I Human chr12 - 112065028 112065028 112065028 TTATTTTTTTATTTTATTTTATTTTTTGAGACAAGTTTCGCTCTTCTTGCCCAGGCTAGAGTGCA TTATTTTTTTATTTTATTTTATTTTTTGAGACGAGTTTCGCTCTTCTTGCCCAGGCTAGAGTGCA T C NAA25 Ensembl:ENSG00000111300 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs757982650 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6134285,Human_RBP_ID_11818961,Human_RBP_ID_24931775 RMVar_hsa_circ_64741,RMVar_hsa_circ_65557,RMVar_hsa_circ_36254,RMVar_hsa_circ_61015,RMVar_hsa_circ_44174,RMVar_hsa_circ_160095,RMVar_hsa_circ_62757,RMVar_hsa_circ_36025,RMVar_hsa_circ_337661,RMVar_hsa_circ_30457,RMVar_hsa_circ_160100,RMVar_hsa_circ_160099,RMVar_hsa_circ_110973,RMVar_hsa_circ_348874,RMVar_hsa_circ_349132,RMVar_hsa_circ_356087,RMVar_hsa_circ_347978,RMVar_hsa_circ_287779,RMVar_hsa_circ_160101,RMVar_hsa_circ_160102,RMVar_hsa_circ_160103 27748 RMVar_ID_27748 Human_SNP_ID_516041140 A-to-I Human chr12 - 112069341 112069341 112069341 TGCTGCCACGCCCAGCTAATTTTTGTACTTTTAGTAGAGATGGGGTTTCACCATGTTGCCAGGCT TGCTGCCACGCCCAGCTAATTTTTGTACTTTTGGTAGAGATGGGGTTTCACCATGTTGCCAGGCT T C NAA25 Ensembl:ENSG00000111300 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1018075512 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64741,RMVar_hsa_circ_65557,RMVar_hsa_circ_36254,RMVar_hsa_circ_44174,RMVar_hsa_circ_160095,RMVar_hsa_circ_36025,RMVar_hsa_circ_337661,RMVar_hsa_circ_30457,RMVar_hsa_circ_160100,RMVar_hsa_circ_160099,RMVar_hsa_circ_110973,RMVar_hsa_circ_348874,RMVar_hsa_circ_349132,RMVar_hsa_circ_356087,RMVar_hsa_circ_347978,RMVar_hsa_circ_287779,RMVar_hsa_circ_33582,RMVar_hsa_circ_310728,RMVar_hsa_circ_160101,RMVar_hsa_circ_160102,RMVar_hsa_circ_160103,RMVar_hsa_circ_329429,RMVar_hsa_circ_349312,RMVar_hsa_circ_311570,RMVar_hsa_circ_291689,RMVar_hsa_circ_292238,RMVar_hsa_circ_52056,RMVar_hsa_circ_160104,RMVar_hsa_circ_160106,RMVar_hsa_circ_160107,RMVar_hsa_circ_160108,RMVar_hsa_circ_160105 27749 RMVar_ID_27749 Human_SNP_ID_516041312 A-to-I Human chr12 - 112069925 112069925 112069925 TGGGGTTTTGCCATGTTGCCCAGGCTGGTCTCAAACTCCTGGACTCAAGTGATCTCCCTACCTTG TGGGGTTTTGCCATGTTGCCCAGGCTGGTCTCGAACTCCTGGACTCAAGTGATCTCCCTACCTTG T C NAA25 Ensembl:ENSG00000111300 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs907697779 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64741,RMVar_hsa_circ_65557,RMVar_hsa_circ_36254,RMVar_hsa_circ_44174,RMVar_hsa_circ_160095,RMVar_hsa_circ_36025,RMVar_hsa_circ_337661,RMVar_hsa_circ_30457,RMVar_hsa_circ_160100,RMVar_hsa_circ_160099,RMVar_hsa_circ_110973,RMVar_hsa_circ_348874,RMVar_hsa_circ_349132,RMVar_hsa_circ_356087,RMVar_hsa_circ_347978,RMVar_hsa_circ_287779,RMVar_hsa_circ_33582,RMVar_hsa_circ_310728,RMVar_hsa_circ_160101,RMVar_hsa_circ_160102,RMVar_hsa_circ_160103,RMVar_hsa_circ_329429,RMVar_hsa_circ_349312,RMVar_hsa_circ_311570,RMVar_hsa_circ_291689,RMVar_hsa_circ_292238,RMVar_hsa_circ_52056,RMVar_hsa_circ_160104,RMVar_hsa_circ_160106,RMVar_hsa_circ_160107,RMVar_hsa_circ_160108,RMVar_hsa_circ_160105 27750 RMVar_ID_27750 Human_SNP_ID_516041536 A-to-I Human chr12 - 112070875 112070875 112070875 AGGCATGGTGGCACACGCCTGTAGTTACAGCTACTTGGGAGGCTGAGGCAGGAGAATTGCTTGAA AGGCATGGTGGCACACGCCTGTAGTTACAGCTCCTTGGGAGGCTGAGGCAGGAGAATTGCTTGAA T G NAA25 Ensembl:ENSG00000111300 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1482824030 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64741,RMVar_hsa_circ_65557,RMVar_hsa_circ_36254,RMVar_hsa_circ_44174,RMVar_hsa_circ_160095,RMVar_hsa_circ_36025,RMVar_hsa_circ_337661,RMVar_hsa_circ_30457,RMVar_hsa_circ_160100,RMVar_hsa_circ_160099,RMVar_hsa_circ_110973,RMVar_hsa_circ_348874,RMVar_hsa_circ_349132,RMVar_hsa_circ_356087,RMVar_hsa_circ_347978,RMVar_hsa_circ_287779,RMVar_hsa_circ_33582,RMVar_hsa_circ_310728,RMVar_hsa_circ_160101,RMVar_hsa_circ_160102,RMVar_hsa_circ_160103,RMVar_hsa_circ_329429,RMVar_hsa_circ_349312,RMVar_hsa_circ_311570,RMVar_hsa_circ_291689,RMVar_hsa_circ_292238,RMVar_hsa_circ_52056,RMVar_hsa_circ_160104,RMVar_hsa_circ_160106,RMVar_hsa_circ_160107,RMVar_hsa_circ_160108,RMVar_hsa_circ_160105 27751 RMVar_ID_27751 Human_SNP_ID_516042936 A-to-I Human chr12 - 112076169 112076169 112076169 TAAGAAAATGTGACATTTAGGCCGGGCCCGGTAGCTCACAGCTGTAATCCCAGCACTCTGGGAGG TAAGAAAATGTGACATTTAGGCCGGGCCCGGTTGCTCACAGCTGTAATCCCAGCACTCTGGGAGG T A NAA25 Ensembl:ENSG00000111300 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs745818496 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6134339,Human_RBP_ID_11819231 RMVar_hsa_circ_65557,RMVar_hsa_circ_36254,RMVar_hsa_circ_21155,RMVar_hsa_circ_44174,RMVar_hsa_circ_160095,RMVar_hsa_circ_337661,RMVar_hsa_circ_30457,RMVar_hsa_circ_160100,RMVar_hsa_circ_160099,RMVar_hsa_circ_110973,RMVar_hsa_circ_349132,RMVar_hsa_circ_356087,RMVar_hsa_circ_33582,RMVar_hsa_circ_160101,RMVar_hsa_circ_160102,RMVar_hsa_circ_349312,RMVar_hsa_circ_311570,RMVar_hsa_circ_291689,RMVar_hsa_circ_292238,RMVar_hsa_circ_160106,RMVar_hsa_circ_160107,RMVar_hsa_circ_160108,RMVar_hsa_circ_279910,RMVar_hsa_circ_303571,RMVar_hsa_circ_345808,RMVar_hsa_circ_160116,RMVar_hsa_circ_65664,RMVar_hsa_circ_160109,RMVar_hsa_circ_160110,RMVar_hsa_circ_307306,RMVar_hsa_circ_160112,RMVar_hsa_circ_288706,RMVar_hsa_circ_311545,RMVar_hsa_circ_342243,RMVar_hsa_circ_291036,RMVar_hsa_circ_160114,RMVar_hsa_circ_160115 27752 RMVar_ID_27752 Human_SNP_ID_516043735 A-to-I Human chr12 - 112079561 112079561 112079561 TAACCTTAGTTTTTTTTTTTTTCTGTTGTCCAAGCTGGAGTGCAGTGGCATGACCTCAGCTTACT TAACCTTAGTTTTTTTTTTTTTCTGTTGTCCATGCTGGAGTGCAGTGGCATGACCTCAGCTTACT T A NAA25 Ensembl:ENSG00000111300 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs377426523 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36254,RMVar_hsa_circ_21155,RMVar_hsa_circ_44174,RMVar_hsa_circ_160095,RMVar_hsa_circ_30457,RMVar_hsa_circ_349132,RMVar_hsa_circ_33582,RMVar_hsa_circ_160101,RMVar_hsa_circ_349312,RMVar_hsa_circ_311570,RMVar_hsa_circ_291689,RMVar_hsa_circ_160107,RMVar_hsa_circ_160108,RMVar_hsa_circ_279910,RMVar_hsa_circ_345808,RMVar_hsa_circ_160116,RMVar_hsa_circ_65664,RMVar_hsa_circ_160110,RMVar_hsa_circ_311545,RMVar_hsa_circ_342243,RMVar_hsa_circ_291036,RMVar_hsa_circ_74981,RMVar_hsa_circ_160115,RMVar_hsa_circ_367315,RMVar_hsa_circ_367571,RMVar_hsa_circ_160117,RMVar_hsa_circ_353607 27753 RMVar_ID_27753 Human_SNP_ID_516046318 A-to-I Human chr12 - 112089827 112089827 112089827 CACCATCCCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGTTTCACCATGTTGGCCGGGCTGGT CACCATCCCCAGCTAATTTTTGTATTTTTAGTTGAGACGGGTTTCACCATGTTGGCCGGGCTGGT T A NAA25 Ensembl:ENSG00000111300 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs934413873 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_349132,RMVar_hsa_circ_33582,RMVar_hsa_circ_291689,RMVar_hsa_circ_279910,RMVar_hsa_circ_160120,RMVar_hsa_circ_160116,RMVar_hsa_circ_160110,RMVar_hsa_circ_311545,RMVar_hsa_circ_367571,RMVar_hsa_circ_160119,RMVar_hsa_circ_353607,RMVar_hsa_circ_325205,RMVar_hsa_circ_326270 27754 RMVar_ID_27754 Human_SNP_ID_516046326 A-to-I Human chr12 - 112089865 112089865 112089865 CCTCGGCTTCCCAGGTAGCTGGGATTACAGGCATGCACCACCATCCCCAGCTAATTTTTGTATTT CCTCGGCTTCCCAGGTAGCTGGGATTACAGGCGTGCACCACCATCCCCAGCTAATTTTTGTATTT T C NAA25 Ensembl:ENSG00000111300 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1417943695 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_349132,RMVar_hsa_circ_33582,RMVar_hsa_circ_291689,RMVar_hsa_circ_279910,RMVar_hsa_circ_160120,RMVar_hsa_circ_160116,RMVar_hsa_circ_160110,RMVar_hsa_circ_311545,RMVar_hsa_circ_367571,RMVar_hsa_circ_160119,RMVar_hsa_circ_353607,RMVar_hsa_circ_325205,RMVar_hsa_circ_326270 27755 RMVar_ID_27755 Human_SNP_ID_516048876 A-to-I Human chr12 - 112100273 112100273 112100273 CCTGTAGTCCCAGCTGCTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCTGGGAGGCAGAGGTT CCTGTAGTCCCAGCTGCTCAGGAGGCTGAGGCGGGAGAATCACTTGAACCTGGGAGGCAGAGGTT T C NAA25 Ensembl:ENSG00000111300 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1366551070 Functional Loss SNV dbSNP153 33..33 33 - - - 27756 RMVar_ID_27756 Human_SNP_ID_516048889 A-to-I Human chr12 - 112100329 112100328 112100329 GTGAAACCCTGTCTCTACTAAAATACAAAAAAATTAGCCAGGCCTGGTGGTACGAGCCTGTAGTC GTGAAACCCTGTCTCTACTAAAATACAAAAAA_TTAGCCAGGCCTGGTGGTACGAGCCTGTAGTC AT A NAA25 Ensembl:ENSG00000111300 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1488739865 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_115613 27757 RMVar_ID_27757 Human_SNP_ID_516048890 A-to-I Human chr12 - 112100329 112100329 112100329 GTGAAACCCTGTCTCTACTAAAATACAAAAAAATTAGCCAGGCCTGGTGGTACGAGCCTGTAGTC GTGAAACCCTGTCTCTACTAAAATACAAAAAAGTTAGCCAGGCCTGGTGGTACGAGCCTGTAGTC T C NAA25 Ensembl:ENSG00000111300 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs541738707 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_115613 27758 RMVar_ID_27758 Human_SNP_ID_516049028 A-to-I Human chr12 - 112100752 112100752 112100752 CTCCGGGCGTGATGGCGGGCGCCTGTAGTCCCAGCTACTCCGGAGGCTGAGGTAGGAGAATGGCG CTCCGGGCGTGATGGCGGGCGCCTGTAGTCCCGGCTACTCCGGAGGCTGAGGTAGGAGAATGGCG T C NAA25 Ensembl:ENSG00000111300 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1426966851 Functional Loss SNV dbSNP153 33..33 33 - - - 27759 RMVar_ID_27759 Human_SNP_ID_516049247 A-to-I Human chr12 - 112101743 112101743 112101743 TTTTTTTGATAGATTTTTTAAGATGCAGTCTCACTCTGTCACCTGGGCTGGAGTGCAATGGCGTG TTTTTTTGATAGATTTTTTAAGATGCAGTCTCGCTCTGTCACCTGGGCTGGAGTGCAATGGCGTG T C NAA25 Ensembl:ENSG00000111300 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1196837493 Functional Loss SNV dbSNP153 33..33 33 - - - 27760 RMVar_ID_27760 Human_SNP_ID_516049533 A-to-I Human chr12 - 112102838 112102838 112102838 TAAAAATATACGAAAAATTAGCCGGGTGTGGTAGTGTGCATCTGTAATCCCAGCTATTCAGAAGG TAAAAATATACGAAAAATTAGCCGGGTGTGGTGGTGTGCATCTGTAATCCCAGCTATTCAGAAGG T C NAA25 Ensembl:ENSG00000111300 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1229761153 Functional Loss SNV dbSNP153 33..33 33 - - - 27761 RMVar_ID_27761 Human_SNP_ID_516050412 A-to-I Human chr12 - 112106722 112106722 112106722 CTAAAACTCCTGAGCTCAAGCAGTCCTGCCTCAGCCTCCCAGAGTGCTGGGATTACAGGTGTGAG CTAAAACTCCTGAGCTCAAGCAGTCCTGCCTCGGCCTCCCAGAGTGCTGGGATTACAGGTGTGAG T C NAA25 Ensembl:ENSG00000111300 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs928400105 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11820275 27762 RMVar_ID_27762 Human_SNP_ID_516050421 A-to-I Human chr12 - 112106762 112106762 112106762 TATTGTAGAGAATGGGTTTCGTCATGTTGCCCAGTCTAGTCTAAAACTCCTGAGCTCAAGCAGTC TATTGTAGAGAATGGGTTTCGTCATGTTGCCCGGTCTAGTCTAAAACTCCTGAGCTCAAGCAGTC T C NAA25 Ensembl:ENSG00000111300 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs573571264 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11820276 27763 RMVar_ID_27763 Human_SNP_ID_516057367 A-to-I Human chr12 + 112136517 112136517 112136517 GTTGGCCAGGGTGATCTTGAACTCCTGACCTCAGGTGATCCACCCACCTTGGCCCCTCAAGGTGC GTTGGCCAGGGTGATCTTGAACTCCTGACCTCTGGTGATCCACCCACCTTGGCCCCTCAAGGTGC A T TRAFD1 Ensembl:ENSG00000135148 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1208653197 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_160123,RMVar_hsa_circ_312915,RMVar_hsa_circ_321263,RMVar_hsa_circ_70337,RMVar_hsa_circ_86434,RMVar_hsa_circ_160124,RMVar_hsa_circ_160125,RMVar_hsa_circ_92130,RMVar_hsa_circ_160127,RMVar_hsa_circ_160128,RMVar_hsa_circ_76049 27764 RMVar_ID_27764 Human_SNP_ID_516057416 A-to-I Human chr12 + 112136807 112136807 112136807 TAGAGTTGGGGTCTTGTTATGTTGCCCAGGCTAGTCTCGAACTCTTGGCCTCAAGTGATCCTCCC TAGAGTTGGGGTCTTGTTATGTTGCCCAGGCTGGTCTCGAACTCTTGGCCTCAAGTGATCCTCCC A G TRAFD1 Ensembl:ENSG00000135148 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1388701339 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_160123,RMVar_hsa_circ_312915,RMVar_hsa_circ_321263,RMVar_hsa_circ_70337,RMVar_hsa_circ_86434,RMVar_hsa_circ_160124,RMVar_hsa_circ_160125,RMVar_hsa_circ_92130,RMVar_hsa_circ_160127,RMVar_hsa_circ_160128,RMVar_hsa_circ_76049 27765 RMVar_ID_27765 Human_SNP_ID_516059693 A-to-I Human chr12 + 112146345 112146345 112146345 GCCCATGAGTTTAAGGCCAGCCTGGGCAACATAGTGAGACCCCAGCTCTACCAAAAAAAAAGGGG GCCCATGAGTTTAAGGCCAGCCTGGGCAACATGGTGAGACCCCAGCTCTACCAAAAAAAAAGGGG A G TRAFD1 Ensembl:ENSG00000135148 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1323676107 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26662,RMVar_hsa_circ_75980,RMVar_hsa_circ_70337,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_46113,RMVar_hsa_circ_345990,RMVar_hsa_circ_345534 27766 RMVar_ID_27766 Human_SNP_ID_516060755 A-to-I Human chr12 + 112150823 112150823 112150823 GGGCTCAAGTGTTCCTCCCAGCTCGGCCTCCCAAAGTGTTGGGATTACAGGTGTGAGCCATCACA GGGCTCAAGTGTTCCTCCCAGCTCGGCCTCCCGAAGTGTTGGGATTACAGGTGTGAGCCATCACA A G TRAFD1 Ensembl:ENSG00000135148 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs927334858 Functional Loss SNV dbSNP153 33..33 33 - - - 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 27767 RMVar_ID_27767 Human_SNP_ID_516060904 A-to-I Human chr12 + 112151492 112151492 112151492 TTGGCTCACTGCAGTCTTCACCTCCTGGGTTTAAGTGATTCTCCTGGTCTCAGCCTCCTGAGTAG TTGGCTCACTGCAGTCTTCACCTCCTGGGTTTCAGTGATTCTCCTGGTCTCAGCCTCCTGAGTAG A C TRAFD1 Ensembl:ENSG00000135148 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1034932229 Functional Loss SNV dbSNP153 33..33 33 - - - 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 27768 RMVar_ID_27768 Human_SNP_ID_516060913 A-to-I Human chr12 + 112151533 112151531 112151533 TCCTGGTCTCAGCCTCCTGAGTAGCTGAGACTATAGCTGTGTGCCACCTCACCTGGCTAATTTTG TCCTGGTCTCAGCCTCCTGAGTAGCTGAGAC__TAGCTGTGTGCCACCTCACCTGGCTAATTTTG CTA C TRAFD1 Ensembl:ENSG00000135148 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs567288656 Functional Loss DEL dbSNP153 32..33 33 - - - 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 27769 RMVar_ID_27769 Human_SNP_ID_516070897 A-to-I Human chr12 - 112189892 112189892 112189892 AAAATTGGCCGGGCATGGTGGTGCATGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGG AAAATTGGCCGGGCATGGTGGTGCATGCCTGTGGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGG T C HECTD4 Ensembl:ENSG00000173064 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1198770433 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76071,RMVar_hsa_circ_266793,RMVar_hsa_circ_269340,RMVar_hsa_circ_92283,RMVar_hsa_circ_265564,RMVar_hsa_circ_86521,RMVar_hsa_circ_59231,RMVar_hsa_circ_96738,RMVar_hsa_circ_160134,RMVar_hsa_circ_160135,RMVar_hsa_circ_160133,RMVar_hsa_circ_86374,RMVar_hsa_circ_160136,RMVar_hsa_circ_160137,RMVar_hsa_circ_266836,RMVar_hsa_circ_16871,RMVar_hsa_circ_160139,RMVar_hsa_circ_120037,RMVar_hsa_circ_56551,RMVar_hsa_circ_17528,RMVar_hsa_circ_78078,RMVar_hsa_circ_90046,RMVar_hsa_circ_110981,RMVar_hsa_circ_269059,RMVar_hsa_circ_269436,RMVar_hsa_circ_120958,RMVar_hsa_circ_99564,RMVar_hsa_circ_104560,RMVar_hsa_circ_99507,RMVar_hsa_circ_82647,RMVar_hsa_circ_88433,RMVar_hsa_circ_79943,RMVar_hsa_circ_98741,RMVar_hsa_circ_160146,RMVar_hsa_circ_160148,RMVar_hsa_circ_160150,RMVar_hsa_circ_160152,RMVar_hsa_circ_160151,RMVar_hsa_circ_160149,RMVar_hsa_circ_160147,RMVar_hsa_circ_160144,RMVar_hsa_circ_160145,RMVar_hsa_circ_160143,RMVar_hsa_circ_92094,RMVar_hsa_circ_160155,RMVar_hsa_circ_81719,RMVar_hsa_circ_160154,RMVar_hsa_circ_12700,RMVar_hsa_circ_160156 27770 RMVar_ID_27770 Human_SNP_ID_516074503 A-to-I Human chr12 - 112205781 112205781 112205781 TGAGACCAGCCTAGGCAACATGGTGAACCCCCATCTCTACTAAAAATACAAAAATATTAGCCGAG TGAGACCAGCCTAGGCAACATGGTGAACCCCCGTCTCTACTAAAAATACAAAAATATTAGCCGAG T C HECTD4 Ensembl:ENSG00000173064 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs538599375 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76071,RMVar_hsa_circ_266793,RMVar_hsa_circ_269340,RMVar_hsa_circ_92283,RMVar_hsa_circ_265564,RMVar_hsa_circ_86521,RMVar_hsa_circ_96738,RMVar_hsa_circ_160134,RMVar_hsa_circ_160135,RMVar_hsa_circ_160133,RMVar_hsa_circ_86374,RMVar_hsa_circ_160136,RMVar_hsa_circ_160137,RMVar_hsa_circ_266836,RMVar_hsa_circ_16871,RMVar_hsa_circ_160139,RMVar_hsa_circ_120037,RMVar_hsa_circ_56551,RMVar_hsa_circ_17528,RMVar_hsa_circ_78078,RMVar_hsa_circ_90046,RMVar_hsa_circ_110981,RMVar_hsa_circ_269059,RMVar_hsa_circ_269436,RMVar_hsa_circ_120958,RMVar_hsa_circ_99564,RMVar_hsa_circ_104560,RMVar_hsa_circ_99507,RMVar_hsa_circ_82647,RMVar_hsa_circ_88433,RMVar_hsa_circ_79943,RMVar_hsa_circ_98741,RMVar_hsa_circ_160146,RMVar_hsa_circ_160148,RMVar_hsa_circ_160150,RMVar_hsa_circ_160152,RMVar_hsa_circ_160151,RMVar_hsa_circ_160149,RMVar_hsa_circ_160147,RMVar_hsa_circ_160144,RMVar_hsa_circ_160145,RMVar_hsa_circ_160143,RMVar_hsa_circ_92094,RMVar_hsa_circ_160155,RMVar_hsa_circ_81719,RMVar_hsa_circ_160154,RMVar_hsa_circ_160156,RMVar_hsa_circ_5824,RMVar_hsa_circ_22381,RMVar_hsa_circ_358670,RMVar_hsa_circ_84481,RMVar_hsa_circ_160158,RMVar_hsa_circ_23033,RMVar_hsa_circ_347738,RMVar_hsa_circ_32340,RMVar_hsa_circ_12086,RMVar_hsa_circ_160161,RMVar_hsa_circ_91992,RMVar_hsa_circ_331663,RMVar_hsa_circ_340174,RMVar_hsa_circ_326154,RMVar_hsa_circ_272179,RMVar_hsa_circ_160163,RMVar_hsa_circ_160164,RMVar_hsa_circ_160162,RMVar_hsa_circ_160167,RMVar_hsa_circ_84639,RMVar_hsa_circ_309283,RMVar_hsa_circ_330623,RMVar_hsa_circ_372646,RMVar_hsa_circ_119357,RMVar_hsa_circ_160169,RMVar_hsa_circ_52073,RMVar_hsa_circ_160170,RMVar_hsa_circ_160168,RMVar_hsa_circ_160166 27771 RMVar_ID_27771 Human_SNP_ID_516074504 A-to-I Human chr12 - 112205781 112205781 112205781 TGAGACCAGCCTAGGCAACATGGTGAACCCCCATCTCTACTAAAAATACAAAAATATTAGCCGAG TGAGACCAGCCTAGGCAACATGGTGAACCCCCCTCTCTACTAAAAATACAAAAATATTAGCCGAG T G HECTD4 Ensembl:ENSG00000173064 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs538599375 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76071,RMVar_hsa_circ_266793,RMVar_hsa_circ_269340,RMVar_hsa_circ_92283,RMVar_hsa_circ_265564,RMVar_hsa_circ_86521,RMVar_hsa_circ_96738,RMVar_hsa_circ_160134,RMVar_hsa_circ_160135,RMVar_hsa_circ_160133,RMVar_hsa_circ_86374,RMVar_hsa_circ_160136,RMVar_hsa_circ_160137,RMVar_hsa_circ_266836,RMVar_hsa_circ_16871,RMVar_hsa_circ_160139,RMVar_hsa_circ_120037,RMVar_hsa_circ_56551,RMVar_hsa_circ_17528,RMVar_hsa_circ_78078,RMVar_hsa_circ_90046,RMVar_hsa_circ_110981,RMVar_hsa_circ_269059,RMVar_hsa_circ_269436,RMVar_hsa_circ_120958,RMVar_hsa_circ_99564,RMVar_hsa_circ_104560,RMVar_hsa_circ_99507,RMVar_hsa_circ_82647,RMVar_hsa_circ_88433,RMVar_hsa_circ_79943,RMVar_hsa_circ_98741,RMVar_hsa_circ_160146,RMVar_hsa_circ_160148,RMVar_hsa_circ_160150,RMVar_hsa_circ_160152,RMVar_hsa_circ_160151,RMVar_hsa_circ_160149,RMVar_hsa_circ_160147,RMVar_hsa_circ_160144,RMVar_hsa_circ_160145,RMVar_hsa_circ_160143,RMVar_hsa_circ_92094,RMVar_hsa_circ_160155,RMVar_hsa_circ_81719,RMVar_hsa_circ_160154,RMVar_hsa_circ_160156,RMVar_hsa_circ_5824,RMVar_hsa_circ_22381,RMVar_hsa_circ_358670,RMVar_hsa_circ_84481,RMVar_hsa_circ_160158,RMVar_hsa_circ_23033,RMVar_hsa_circ_347738,RMVar_hsa_circ_32340,RMVar_hsa_circ_12086,RMVar_hsa_circ_160161,RMVar_hsa_circ_91992,RMVar_hsa_circ_331663,RMVar_hsa_circ_340174,RMVar_hsa_circ_326154,RMVar_hsa_circ_272179,RMVar_hsa_circ_160163,RMVar_hsa_circ_160164,RMVar_hsa_circ_160162,RMVar_hsa_circ_160167,RMVar_hsa_circ_84639,RMVar_hsa_circ_309283,RMVar_hsa_circ_330623,RMVar_hsa_circ_372646,RMVar_hsa_circ_119357,RMVar_hsa_circ_160169,RMVar_hsa_circ_52073,RMVar_hsa_circ_160170,RMVar_hsa_circ_160168,RMVar_hsa_circ_160166 27772 RMVar_ID_27772 Human_SNP_ID_516074515 A-to-I Human chr12 - 112205840 112205840 112205840 CCTGTAATCTCAGCACTTTGGAAGGCCAAGGCAGGCGGATCACTTGAGGTCAGGAGTTTTGAGAC CCTGTAATCTCAGCACTTTGGAAGGCCAAGGCGGGCGGATCACTTGAGGTCAGGAGTTTTGAGAC T C HECTD4 Ensembl:ENSG00000173064 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1025152446 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76071,RMVar_hsa_circ_266793,RMVar_hsa_circ_269340,RMVar_hsa_circ_92283,RMVar_hsa_circ_265564,RMVar_hsa_circ_86521,RMVar_hsa_circ_96738,RMVar_hsa_circ_160134,RMVar_hsa_circ_160135,RMVar_hsa_circ_160133,RMVar_hsa_circ_86374,RMVar_hsa_circ_160136,RMVar_hsa_circ_160137,RMVar_hsa_circ_266836,RMVar_hsa_circ_16871,RMVar_hsa_circ_160139,RMVar_hsa_circ_120037,RMVar_hsa_circ_56551,RMVar_hsa_circ_17528,RMVar_hsa_circ_78078,RMVar_hsa_circ_90046,RMVar_hsa_circ_110981,RMVar_hsa_circ_269059,RMVar_hsa_circ_269436,RMVar_hsa_circ_120958,RMVar_hsa_circ_99564,RMVar_hsa_circ_104560,RMVar_hsa_circ_99507,RMVar_hsa_circ_82647,RMVar_hsa_circ_88433,RMVar_hsa_circ_79943,RMVar_hsa_circ_98741,RMVar_hsa_circ_160146,RMVar_hsa_circ_160148,RMVar_hsa_circ_160150,RMVar_hsa_circ_160152,RMVar_hsa_circ_160151,RMVar_hsa_circ_160149,RMVar_hsa_circ_160147,RMVar_hsa_circ_160144,RMVar_hsa_circ_160145,RMVar_hsa_circ_160143,RMVar_hsa_circ_92094,RMVar_hsa_circ_160155,RMVar_hsa_circ_81719,RMVar_hsa_circ_160154,RMVar_hsa_circ_160156,RMVar_hsa_circ_5824,RMVar_hsa_circ_22381,RMVar_hsa_circ_358670,RMVar_hsa_circ_84481,RMVar_hsa_circ_160158,RMVar_hsa_circ_23033,RMVar_hsa_circ_347738,RMVar_hsa_circ_32340,RMVar_hsa_circ_12086,RMVar_hsa_circ_160161,RMVar_hsa_circ_91992,RMVar_hsa_circ_331663,RMVar_hsa_circ_340174,RMVar_hsa_circ_326154,RMVar_hsa_circ_272179,RMVar_hsa_circ_160163,RMVar_hsa_circ_160164,RMVar_hsa_circ_160162,RMVar_hsa_circ_160167,RMVar_hsa_circ_84639,RMVar_hsa_circ_309283,RMVar_hsa_circ_330623,RMVar_hsa_circ_372646,RMVar_hsa_circ_119357,RMVar_hsa_circ_160169,RMVar_hsa_circ_52073,RMVar_hsa_circ_160170,RMVar_hsa_circ_160168,RMVar_hsa_circ_160166 27773 RMVar_ID_27773 Human_SNP_ID_516074626 A-to-I Human chr12 - 112206373 112206373 112206373 CTCCTGCTTCAGCTTCCCGAGTACCTGGGACTACAGGCACTCACTACCAAGCCTGGCTAATTTTT CTCCTGCTTCAGCTTCCCGAGTACCTGGGACTGCAGGCACTCACTACCAAGCCTGGCTAATTTTT T C HECTD4 Ensembl:ENSG00000173064 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs563612474 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76071,RMVar_hsa_circ_266793,RMVar_hsa_circ_269340,RMVar_hsa_circ_92283,RMVar_hsa_circ_265564,RMVar_hsa_circ_86521,RMVar_hsa_circ_96738,RMVar_hsa_circ_160134,RMVar_hsa_circ_160135,RMVar_hsa_circ_160133,RMVar_hsa_circ_86374,RMVar_hsa_circ_160136,RMVar_hsa_circ_160137,RMVar_hsa_circ_266836,RMVar_hsa_circ_16871,RMVar_hsa_circ_160139,RMVar_hsa_circ_120037,RMVar_hsa_circ_56551,RMVar_hsa_circ_17528,RMVar_hsa_circ_78078,RMVar_hsa_circ_90046,RMVar_hsa_circ_110981,RMVar_hsa_circ_269059,RMVar_hsa_circ_269436,RMVar_hsa_circ_120958,RMVar_hsa_circ_99564,RMVar_hsa_circ_104560,RMVar_hsa_circ_99507,RMVar_hsa_circ_82647,RMVar_hsa_circ_88433,RMVar_hsa_circ_79943,RMVar_hsa_circ_98741,RMVar_hsa_circ_160146,RMVar_hsa_circ_160148,RMVar_hsa_circ_160150,RMVar_hsa_circ_160152,RMVar_hsa_circ_160151,RMVar_hsa_circ_160149,RMVar_hsa_circ_160147,RMVar_hsa_circ_160144,RMVar_hsa_circ_160145,RMVar_hsa_circ_160143,RMVar_hsa_circ_92094,RMVar_hsa_circ_160155,RMVar_hsa_circ_81719,RMVar_hsa_circ_160154,RMVar_hsa_circ_160156,RMVar_hsa_circ_5824,RMVar_hsa_circ_22381,RMVar_hsa_circ_358670,RMVar_hsa_circ_84481,RMVar_hsa_circ_160158,RMVar_hsa_circ_23033,RMVar_hsa_circ_347738,RMVar_hsa_circ_32340,RMVar_hsa_circ_12086,RMVar_hsa_circ_160161,RMVar_hsa_circ_91992,RMVar_hsa_circ_331663,RMVar_hsa_circ_340174,RMVar_hsa_circ_326154,RMVar_hsa_circ_272179,RMVar_hsa_circ_160163,RMVar_hsa_circ_160164,RMVar_hsa_circ_160162,RMVar_hsa_circ_160167,RMVar_hsa_circ_84639,RMVar_hsa_circ_309283,RMVar_hsa_circ_330623,RMVar_hsa_circ_372646,RMVar_hsa_circ_119357,RMVar_hsa_circ_160169,RMVar_hsa_circ_52073,RMVar_hsa_circ_160170,RMVar_hsa_circ_160168,RMVar_hsa_circ_160166 27774 RMVar_ID_27774 Human_SNP_ID_516078023 A-to-I Human chr12 - 112220562 112220562 112220562 GAACTTCTGGCCTCAAGTGATCCGTCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAG GAACTTCTGGCCTCAAGTGATCCGTCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAG T C HECTD4 Ensembl:ENSG00000173064 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs759801480 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76071,RMVar_hsa_circ_92283,RMVar_hsa_circ_86521,RMVar_hsa_circ_96738,RMVar_hsa_circ_160134,RMVar_hsa_circ_160135,RMVar_hsa_circ_160133,RMVar_hsa_circ_86374,RMVar_hsa_circ_160136,RMVar_hsa_circ_160137,RMVar_hsa_circ_160139,RMVar_hsa_circ_120037,RMVar_hsa_circ_56551,RMVar_hsa_circ_17528,RMVar_hsa_circ_78078,RMVar_hsa_circ_110981,RMVar_hsa_circ_269059,RMVar_hsa_circ_269436,RMVar_hsa_circ_120958,RMVar_hsa_circ_99564,RMVar_hsa_circ_104560,RMVar_hsa_circ_99507,RMVar_hsa_circ_82647,RMVar_hsa_circ_88433,RMVar_hsa_circ_98741,RMVar_hsa_circ_160146,RMVar_hsa_circ_160148,RMVar_hsa_circ_160150,RMVar_hsa_circ_160149,RMVar_hsa_circ_160147,RMVar_hsa_circ_160144,RMVar_hsa_circ_160145,RMVar_hsa_circ_160143,RMVar_hsa_circ_92094,RMVar_hsa_circ_160155,RMVar_hsa_circ_81719,RMVar_hsa_circ_160154,RMVar_hsa_circ_160156,RMVar_hsa_circ_22381,RMVar_hsa_circ_84481,RMVar_hsa_circ_160158,RMVar_hsa_circ_23033,RMVar_hsa_circ_347738,RMVar_hsa_circ_12086,RMVar_hsa_circ_160161,RMVar_hsa_circ_91992,RMVar_hsa_circ_326154,RMVar_hsa_circ_272179,RMVar_hsa_circ_160162,RMVar_hsa_circ_160167,RMVar_hsa_circ_84639,RMVar_hsa_circ_309283,RMVar_hsa_circ_330623,RMVar_hsa_circ_119357,RMVar_hsa_circ_160169,RMVar_hsa_circ_160170,RMVar_hsa_circ_160168,RMVar_hsa_circ_114242,RMVar_hsa_circ_344036,RMVar_hsa_circ_18248,RMVar_hsa_circ_123644,RMVar_hsa_circ_306661,RMVar_hsa_circ_160171,RMVar_hsa_circ_160177,RMVar_hsa_circ_339207,RMVar_hsa_circ_313462,RMVar_hsa_circ_116076,RMVar_hsa_circ_85907,RMVar_hsa_circ_80308,RMVar_hsa_circ_160178,RMVar_hsa_circ_160180,RMVar_hsa_circ_160181,RMVar_hsa_circ_160179,RMVar_hsa_circ_40416,RMVar_hsa_circ_269460,RMVar_hsa_circ_160184,RMVar_hsa_circ_288211,RMVar_hsa_circ_52366,RMVar_hsa_circ_160185 27775 RMVar_ID_27775 Human_SNP_ID_516078034 A-to-I Human chr12 - 112220631 112220631 112220631 CACCATGCCTGGCTAATTTTTGTATTTTTTGTAGACATGGTGGTTTGCTGTGTTGGCCAGGCTGG CACCATGCCTGGCTAATTTTTGTATTTTTTGTGGACATGGTGGTTTGCTGTGTTGGCCAGGCTGG T C HECTD4 Ensembl:ENSG00000173064 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334632294 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11821064 RMVar_hsa_circ_76071,RMVar_hsa_circ_92283,RMVar_hsa_circ_86521,RMVar_hsa_circ_96738,RMVar_hsa_circ_160134,RMVar_hsa_circ_160135,RMVar_hsa_circ_160133,RMVar_hsa_circ_86374,RMVar_hsa_circ_160136,RMVar_hsa_circ_160137,RMVar_hsa_circ_160139,RMVar_hsa_circ_120037,RMVar_hsa_circ_56551,RMVar_hsa_circ_17528,RMVar_hsa_circ_78078,RMVar_hsa_circ_110981,RMVar_hsa_circ_269059,RMVar_hsa_circ_269436,RMVar_hsa_circ_120958,RMVar_hsa_circ_99564,RMVar_hsa_circ_104560,RMVar_hsa_circ_99507,RMVar_hsa_circ_82647,RMVar_hsa_circ_88433,RMVar_hsa_circ_98741,RMVar_hsa_circ_160146,RMVar_hsa_circ_160148,RMVar_hsa_circ_160150,RMVar_hsa_circ_160149,RMVar_hsa_circ_160147,RMVar_hsa_circ_160144,RMVar_hsa_circ_160145,RMVar_hsa_circ_160143,RMVar_hsa_circ_92094,RMVar_hsa_circ_160155,RMVar_hsa_circ_81719,RMVar_hsa_circ_160154,RMVar_hsa_circ_160156,RMVar_hsa_circ_22381,RMVar_hsa_circ_84481,RMVar_hsa_circ_160158,RMVar_hsa_circ_23033,RMVar_hsa_circ_347738,RMVar_hsa_circ_12086,RMVar_hsa_circ_160161,RMVar_hsa_circ_91992,RMVar_hsa_circ_326154,RMVar_hsa_circ_272179,RMVar_hsa_circ_160162,RMVar_hsa_circ_160167,RMVar_hsa_circ_84639,RMVar_hsa_circ_309283,RMVar_hsa_circ_330623,RMVar_hsa_circ_119357,RMVar_hsa_circ_160169,RMVar_hsa_circ_160170,RMVar_hsa_circ_160168,RMVar_hsa_circ_114242,RMVar_hsa_circ_344036,RMVar_hsa_circ_18248,RMVar_hsa_circ_123644,RMVar_hsa_circ_306661,RMVar_hsa_circ_160171,RMVar_hsa_circ_160177,RMVar_hsa_circ_339207,RMVar_hsa_circ_313462,RMVar_hsa_circ_116076,RMVar_hsa_circ_85907,RMVar_hsa_circ_80308,RMVar_hsa_circ_160178,RMVar_hsa_circ_160180,RMVar_hsa_circ_160181,RMVar_hsa_circ_160179,RMVar_hsa_circ_40416,RMVar_hsa_circ_269460,RMVar_hsa_circ_160184,RMVar_hsa_circ_288211,RMVar_hsa_circ_52366,RMVar_hsa_circ_160185 27776 RMVar_ID_27776 Human_SNP_ID_516078058 A-to-I Human chr12 - 112220735 112220735 112220735 TGGAATGCAGTGGCATGATGTCAGCTCACTGCAACCTCTGCCTCCTGGGTTCAAGCGATTATCAT TGGAATGCAGTGGCATGATGTCAGCTCACTGCTACCTCTGCCTCCTGGGTTCAAGCGATTATCAT T A HECTD4 Ensembl:ENSG00000173064 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1162271669 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76071,RMVar_hsa_circ_92283,RMVar_hsa_circ_86521,RMVar_hsa_circ_96738,RMVar_hsa_circ_160134,RMVar_hsa_circ_160135,RMVar_hsa_circ_160133,RMVar_hsa_circ_86374,RMVar_hsa_circ_160136,RMVar_hsa_circ_160137,RMVar_hsa_circ_160139,RMVar_hsa_circ_120037,RMVar_hsa_circ_56551,RMVar_hsa_circ_17528,RMVar_hsa_circ_78078,RMVar_hsa_circ_110981,RMVar_hsa_circ_269059,RMVar_hsa_circ_269436,RMVar_hsa_circ_120958,RMVar_hsa_circ_99564,RMVar_hsa_circ_104560,RMVar_hsa_circ_99507,RMVar_hsa_circ_82647,RMVar_hsa_circ_88433,RMVar_hsa_circ_98741,RMVar_hsa_circ_160146,RMVar_hsa_circ_160148,RMVar_hsa_circ_160150,RMVar_hsa_circ_160149,RMVar_hsa_circ_160147,RMVar_hsa_circ_160144,RMVar_hsa_circ_160145,RMVar_hsa_circ_160143,RMVar_hsa_circ_92094,RMVar_hsa_circ_160155,RMVar_hsa_circ_81719,RMVar_hsa_circ_160154,RMVar_hsa_circ_160156,RMVar_hsa_circ_22381,RMVar_hsa_circ_84481,RMVar_hsa_circ_160158,RMVar_hsa_circ_23033,RMVar_hsa_circ_347738,RMVar_hsa_circ_12086,RMVar_hsa_circ_160161,RMVar_hsa_circ_91992,RMVar_hsa_circ_326154,RMVar_hsa_circ_272179,RMVar_hsa_circ_160162,RMVar_hsa_circ_160167,RMVar_hsa_circ_84639,RMVar_hsa_circ_309283,RMVar_hsa_circ_330623,RMVar_hsa_circ_119357,RMVar_hsa_circ_160169,RMVar_hsa_circ_160170,RMVar_hsa_circ_160168,RMVar_hsa_circ_114242,RMVar_hsa_circ_344036,RMVar_hsa_circ_18248,RMVar_hsa_circ_123644,RMVar_hsa_circ_306661,RMVar_hsa_circ_160171,RMVar_hsa_circ_160177,RMVar_hsa_circ_339207,RMVar_hsa_circ_313462,RMVar_hsa_circ_116076,RMVar_hsa_circ_85907,RMVar_hsa_circ_80308,RMVar_hsa_circ_160178,RMVar_hsa_circ_160180,RMVar_hsa_circ_160181,RMVar_hsa_circ_160179,RMVar_hsa_circ_40416,RMVar_hsa_circ_269460,RMVar_hsa_circ_160184,RMVar_hsa_circ_288211,RMVar_hsa_circ_52366,RMVar_hsa_circ_160185 27777 RMVar_ID_27777 Human_SNP_ID_516078068 A-to-I Human chr12 - 112220783 112220783 112220783 TCTCTTGTTTATTTATTTAGAGACAGAGTCTCACTCTGTCACCCAGGCTGGAATGCAGTGGCATG TCTCTTGTTTATTTATTTAGAGACAGAGTCTCTCTCTGTCACCCAGGCTGGAATGCAGTGGCATG T A HECTD4 Ensembl:ENSG00000173064 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1566077388 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76071,RMVar_hsa_circ_92283,RMVar_hsa_circ_86521,RMVar_hsa_circ_96738,RMVar_hsa_circ_160134,RMVar_hsa_circ_160135,RMVar_hsa_circ_160133,RMVar_hsa_circ_86374,RMVar_hsa_circ_160136,RMVar_hsa_circ_160137,RMVar_hsa_circ_160139,RMVar_hsa_circ_120037,RMVar_hsa_circ_56551,RMVar_hsa_circ_17528,RMVar_hsa_circ_78078,RMVar_hsa_circ_110981,RMVar_hsa_circ_269059,RMVar_hsa_circ_269436,RMVar_hsa_circ_120958,RMVar_hsa_circ_99564,RMVar_hsa_circ_104560,RMVar_hsa_circ_99507,RMVar_hsa_circ_82647,RMVar_hsa_circ_88433,RMVar_hsa_circ_98741,RMVar_hsa_circ_160146,RMVar_hsa_circ_160148,RMVar_hsa_circ_160150,RMVar_hsa_circ_160149,RMVar_hsa_circ_160147,RMVar_hsa_circ_160144,RMVar_hsa_circ_160145,RMVar_hsa_circ_160143,RMVar_hsa_circ_92094,RMVar_hsa_circ_160155,RMVar_hsa_circ_81719,RMVar_hsa_circ_160154,RMVar_hsa_circ_160156,RMVar_hsa_circ_22381,RMVar_hsa_circ_84481,RMVar_hsa_circ_160158,RMVar_hsa_circ_23033,RMVar_hsa_circ_347738,RMVar_hsa_circ_12086,RMVar_hsa_circ_160161,RMVar_hsa_circ_91992,RMVar_hsa_circ_326154,RMVar_hsa_circ_272179,RMVar_hsa_circ_160162,RMVar_hsa_circ_160167,RMVar_hsa_circ_84639,RMVar_hsa_circ_309283,RMVar_hsa_circ_330623,RMVar_hsa_circ_119357,RMVar_hsa_circ_160169,RMVar_hsa_circ_160170,RMVar_hsa_circ_160168,RMVar_hsa_circ_114242,RMVar_hsa_circ_344036,RMVar_hsa_circ_18248,RMVar_hsa_circ_123644,RMVar_hsa_circ_306661,RMVar_hsa_circ_160171,RMVar_hsa_circ_160177,RMVar_hsa_circ_339207,RMVar_hsa_circ_313462,RMVar_hsa_circ_116076,RMVar_hsa_circ_85907,RMVar_hsa_circ_80308,RMVar_hsa_circ_160178,RMVar_hsa_circ_160180,RMVar_hsa_circ_160181,RMVar_hsa_circ_160179,RMVar_hsa_circ_40416,RMVar_hsa_circ_269460,RMVar_hsa_circ_160184,RMVar_hsa_circ_288211,RMVar_hsa_circ_52366,RMVar_hsa_circ_160185 27778 RMVar_ID_27778 Human_SNP_ID_516078424 A-to-I Human chr12 - 112222123 112222123 112222123 AGGTCAGGAGTTCAAGACTGCCTGGCCAAGATAGTGAAACCCCGTCTCTACTAAAAATACAAAAA AGGTCAGGAGTTCAAGACTGCCTGGCCAAGATGGTGAAACCCCGTCTCTACTAAAAATACAAAAA T C HECTD4 Ensembl:ENSG00000173064 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1470084119 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76071,RMVar_hsa_circ_92283,RMVar_hsa_circ_86521,RMVar_hsa_circ_96738,RMVar_hsa_circ_160134,RMVar_hsa_circ_160135,RMVar_hsa_circ_160133,RMVar_hsa_circ_86374,RMVar_hsa_circ_160136,RMVar_hsa_circ_160137,RMVar_hsa_circ_160139,RMVar_hsa_circ_120037,RMVar_hsa_circ_56551,RMVar_hsa_circ_17528,RMVar_hsa_circ_78078,RMVar_hsa_circ_110981,RMVar_hsa_circ_269059,RMVar_hsa_circ_269436,RMVar_hsa_circ_120958,RMVar_hsa_circ_99564,RMVar_hsa_circ_104560,RMVar_hsa_circ_99507,RMVar_hsa_circ_82647,RMVar_hsa_circ_88433,RMVar_hsa_circ_98741,RMVar_hsa_circ_160146,RMVar_hsa_circ_160148,RMVar_hsa_circ_160150,RMVar_hsa_circ_160149,RMVar_hsa_circ_160147,RMVar_hsa_circ_160144,RMVar_hsa_circ_160145,RMVar_hsa_circ_160143,RMVar_hsa_circ_92094,RMVar_hsa_circ_160155,RMVar_hsa_circ_81719,RMVar_hsa_circ_160154,RMVar_hsa_circ_160156,RMVar_hsa_circ_22381,RMVar_hsa_circ_84481,RMVar_hsa_circ_160158,RMVar_hsa_circ_23033,RMVar_hsa_circ_347738,RMVar_hsa_circ_12086,RMVar_hsa_circ_160161,RMVar_hsa_circ_91992,RMVar_hsa_circ_326154,RMVar_hsa_circ_272179,RMVar_hsa_circ_160162,RMVar_hsa_circ_160167,RMVar_hsa_circ_84639,RMVar_hsa_circ_309283,RMVar_hsa_circ_330623,RMVar_hsa_circ_119357,RMVar_hsa_circ_160169,RMVar_hsa_circ_160170,RMVar_hsa_circ_160168,RMVar_hsa_circ_114242,RMVar_hsa_circ_344036,RMVar_hsa_circ_18248,RMVar_hsa_circ_123644,RMVar_hsa_circ_306661,RMVar_hsa_circ_160171,RMVar_hsa_circ_160177,RMVar_hsa_circ_339207,RMVar_hsa_circ_313462,RMVar_hsa_circ_116076,RMVar_hsa_circ_85907,RMVar_hsa_circ_80308,RMVar_hsa_circ_160178,RMVar_hsa_circ_160180,RMVar_hsa_circ_160181,RMVar_hsa_circ_160179,RMVar_hsa_circ_40416,RMVar_hsa_circ_269460,RMVar_hsa_circ_160184,RMVar_hsa_circ_288211,RMVar_hsa_circ_52366,RMVar_hsa_circ_160185 27779 RMVar_ID_27779 Human_SNP_ID_516078552 A-to-I Human chr12 - 112222661 112222661 112222661 CCCGGCTAATTTTTTGTTTGTTTTTAAAAGACAGAGTCTCACTCTGTTGCCCAGGCTGGAGTGCG CCCGGCTAATTTTTTGTTTGTTTTTAAAAGACGGAGTCTCACTCTGTTGCCCAGGCTGGAGTGCG T C HECTD4 Ensembl:ENSG00000173064 Protein coding intron GSE38233;GSE107867 cultured B-cells;ASD brains,Fragile X samples from NIH NeuroBioBank - 24183664,30559470 RNA-Seq:(High) rs1235291677 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76071,RMVar_hsa_circ_92283,RMVar_hsa_circ_86521,RMVar_hsa_circ_96738,RMVar_hsa_circ_160134,RMVar_hsa_circ_160135,RMVar_hsa_circ_160133,RMVar_hsa_circ_86374,RMVar_hsa_circ_160136,RMVar_hsa_circ_160137,RMVar_hsa_circ_160139,RMVar_hsa_circ_120037,RMVar_hsa_circ_56551,RMVar_hsa_circ_17528,RMVar_hsa_circ_78078,RMVar_hsa_circ_110981,RMVar_hsa_circ_269059,RMVar_hsa_circ_269436,RMVar_hsa_circ_120958,RMVar_hsa_circ_99564,RMVar_hsa_circ_104560,RMVar_hsa_circ_99507,RMVar_hsa_circ_82647,RMVar_hsa_circ_88433,RMVar_hsa_circ_98741,RMVar_hsa_circ_160146,RMVar_hsa_circ_160148,RMVar_hsa_circ_160150,RMVar_hsa_circ_160149,RMVar_hsa_circ_160147,RMVar_hsa_circ_160144,RMVar_hsa_circ_160145,RMVar_hsa_circ_160143,RMVar_hsa_circ_92094,RMVar_hsa_circ_160155,RMVar_hsa_circ_81719,RMVar_hsa_circ_160154,RMVar_hsa_circ_160156,RMVar_hsa_circ_22381,RMVar_hsa_circ_84481,RMVar_hsa_circ_160158,RMVar_hsa_circ_23033,RMVar_hsa_circ_347738,RMVar_hsa_circ_12086,RMVar_hsa_circ_160161,RMVar_hsa_circ_91992,RMVar_hsa_circ_326154,RMVar_hsa_circ_272179,RMVar_hsa_circ_160162,RMVar_hsa_circ_160167,RMVar_hsa_circ_84639,RMVar_hsa_circ_309283,RMVar_hsa_circ_330623,RMVar_hsa_circ_119357,RMVar_hsa_circ_160169,RMVar_hsa_circ_160170,RMVar_hsa_circ_160168,RMVar_hsa_circ_114242,RMVar_hsa_circ_344036,RMVar_hsa_circ_18248,RMVar_hsa_circ_123644,RMVar_hsa_circ_306661,RMVar_hsa_circ_160171,RMVar_hsa_circ_160177,RMVar_hsa_circ_339207,RMVar_hsa_circ_313462,RMVar_hsa_circ_116076,RMVar_hsa_circ_85907,RMVar_hsa_circ_80308,RMVar_hsa_circ_160178,RMVar_hsa_circ_160180,RMVar_hsa_circ_160181,RMVar_hsa_circ_160179,RMVar_hsa_circ_40416,RMVar_hsa_circ_269460,RMVar_hsa_circ_160184,RMVar_hsa_circ_288211,RMVar_hsa_circ_52366,RMVar_hsa_circ_160185 27780 RMVar_ID_27780 Human_SNP_ID_516084322 A-to-I Human chr12 - 112248709 112248709 112248709 GAGCATGGCAGCATGCACCTGTAGTCTCAGCTACCTGGGAGGCTGAGGCAGGAGGATCCCTTGAG GAGCATGGCAGCATGCACCTGTAGTCTCAGCTCCCTGGGAGGCTGAGGCAGGAGGATCCCTTGAG T G HECTD4 Ensembl:ENSG00000173064 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs527943586 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92283,RMVar_hsa_circ_96738,RMVar_hsa_circ_160133,RMVar_hsa_circ_160136,RMVar_hsa_circ_99564,RMVar_hsa_circ_104560,RMVar_hsa_circ_99507,RMVar_hsa_circ_82647,RMVar_hsa_circ_160146,RMVar_hsa_circ_160144,RMVar_hsa_circ_160145,RMVar_hsa_circ_160143,RMVar_hsa_circ_92094,RMVar_hsa_circ_160155,RMVar_hsa_circ_81719,RMVar_hsa_circ_160156,RMVar_hsa_circ_160161,RMVar_hsa_circ_91992,RMVar_hsa_circ_3298,RMVar_hsa_circ_123644,RMVar_hsa_circ_160177,RMVar_hsa_circ_116076,RMVar_hsa_circ_160178,RMVar_hsa_circ_52366,RMVar_hsa_circ_6979,RMVar_hsa_circ_5032,RMVar_hsa_circ_124338,RMVar_hsa_circ_100885,RMVar_hsa_circ_160190,RMVar_hsa_circ_160191,RMVar_hsa_circ_337983,RMVar_hsa_circ_123014,RMVar_hsa_circ_16384,RMVar_hsa_circ_160192,RMVar_hsa_circ_160194,RMVar_hsa_circ_160193,RMVar_hsa_circ_102732,RMVar_hsa_circ_160199,RMVar_hsa_circ_351375,RMVar_hsa_circ_327801,RMVar_hsa_circ_121752,RMVar_hsa_circ_92637,RMVar_hsa_circ_108722,RMVar_hsa_circ_160205,RMVar_hsa_circ_160206,RMVar_hsa_circ_160204,RMVar_hsa_circ_356097,RMVar_hsa_circ_114486,RMVar_hsa_circ_160208,RMVar_hsa_circ_91982,RMVar_hsa_circ_160210,RMVar_hsa_circ_160209,RMVar_hsa_circ_160213,RMVar_hsa_circ_288616,RMVar_hsa_circ_160214,RMVar_hsa_circ_160215,RMVar_hsa_circ_110740 27781 RMVar_ID_27781 Human_SNP_ID_516088595 A-to-I Human chr12 - 112268110 112268110 112268110 TCAATTAAAAAAGAAAAGAGGCTGAGTGTGTTAGCTCATGCCTGTAATCCCCAGCACTTTGAGGG TCAATTAAAAAAGAAAAGAGGCTGAGTGTGTTTGCTCATGCCTGTAATCCCCAGCACTTTGAGGG T A HECTD4 Ensembl:ENSG00000173064 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs939359192 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24933011 RMVar_hsa_circ_92283,RMVar_hsa_circ_96738,RMVar_hsa_circ_160133,RMVar_hsa_circ_160136,RMVar_hsa_circ_99564,RMVar_hsa_circ_104560,RMVar_hsa_circ_82647,RMVar_hsa_circ_160144,RMVar_hsa_circ_160145,RMVar_hsa_circ_160143,RMVar_hsa_circ_92094,RMVar_hsa_circ_160156,RMVar_hsa_circ_160161,RMVar_hsa_circ_91992,RMVar_hsa_circ_3298,RMVar_hsa_circ_102732,RMVar_hsa_circ_160199,RMVar_hsa_circ_92637,RMVar_hsa_circ_160206,RMVar_hsa_circ_114486,RMVar_hsa_circ_160208,RMVar_hsa_circ_11102,RMVar_hsa_circ_3614,RMVar_hsa_circ_160215,RMVar_hsa_circ_110740,RMVar_hsa_circ_160216,RMVar_hsa_circ_18170,RMVar_hsa_circ_160217,RMVar_hsa_circ_5421,RMVar_hsa_circ_266808,RMVar_hsa_circ_369326,RMVar_hsa_circ_160222,RMVar_hsa_circ_1205,RMVar_hsa_circ_66882,RMVar_hsa_circ_25778,RMVar_hsa_circ_13763,RMVar_hsa_circ_125121,RMVar_hsa_circ_335564,RMVar_hsa_circ_40873,RMVar_hsa_circ_24897,RMVar_hsa_circ_160224,RMVar_hsa_circ_47851,RMVar_hsa_circ_281492,RMVar_hsa_circ_343751,RMVar_hsa_circ_98406,RMVar_hsa_circ_18891,RMVar_hsa_circ_160225,RMVar_hsa_circ_160227,RMVar_hsa_circ_160226,RMVar_hsa_circ_62987,RMVar_hsa_circ_301698,RMVar_hsa_circ_279524,RMVar_hsa_circ_289791,RMVar_hsa_circ_44401,RMVar_hsa_circ_160230,RMVar_hsa_circ_160231 27782 RMVar_ID_27782 Human_SNP_ID_516088596 A-to-I Human chr12 - 112268110 112268110 112268110 TCAATTAAAAAAGAAAAGAGGCTGAGTGTGTTAGCTCATGCCTGTAATCCCCAGCACTTTGAGGG TCAATTAAAAAAGAAAAGAGGCTGAGTGTGTTGGCTCATGCCTGTAATCCCCAGCACTTTGAGGG T C HECTD4 Ensembl:ENSG00000173064 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs939359192 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24933011 RMVar_hsa_circ_92283,RMVar_hsa_circ_96738,RMVar_hsa_circ_160133,RMVar_hsa_circ_160136,RMVar_hsa_circ_99564,RMVar_hsa_circ_104560,RMVar_hsa_circ_82647,RMVar_hsa_circ_160144,RMVar_hsa_circ_160145,RMVar_hsa_circ_160143,RMVar_hsa_circ_92094,RMVar_hsa_circ_160156,RMVar_hsa_circ_160161,RMVar_hsa_circ_91992,RMVar_hsa_circ_3298,RMVar_hsa_circ_102732,RMVar_hsa_circ_160199,RMVar_hsa_circ_92637,RMVar_hsa_circ_160206,RMVar_hsa_circ_114486,RMVar_hsa_circ_160208,RMVar_hsa_circ_11102,RMVar_hsa_circ_3614,RMVar_hsa_circ_160215,RMVar_hsa_circ_110740,RMVar_hsa_circ_160216,RMVar_hsa_circ_18170,RMVar_hsa_circ_160217,RMVar_hsa_circ_5421,RMVar_hsa_circ_266808,RMVar_hsa_circ_369326,RMVar_hsa_circ_160222,RMVar_hsa_circ_1205,RMVar_hsa_circ_66882,RMVar_hsa_circ_25778,RMVar_hsa_circ_13763,RMVar_hsa_circ_125121,RMVar_hsa_circ_335564,RMVar_hsa_circ_40873,RMVar_hsa_circ_24897,RMVar_hsa_circ_160224,RMVar_hsa_circ_47851,RMVar_hsa_circ_281492,RMVar_hsa_circ_343751,RMVar_hsa_circ_98406,RMVar_hsa_circ_18891,RMVar_hsa_circ_160225,RMVar_hsa_circ_160227,RMVar_hsa_circ_160226,RMVar_hsa_circ_62987,RMVar_hsa_circ_301698,RMVar_hsa_circ_279524,RMVar_hsa_circ_289791,RMVar_hsa_circ_44401,RMVar_hsa_circ_160230,RMVar_hsa_circ_160231 27783 RMVar_ID_27783 Human_SNP_ID_516093152 A-to-I Human chr12 - 112289168 112289168 112289168 TTGAGCCCTGAAGGTCAAGGCTGCAGTGAGCCATGATCGTGCCACTGCACTCCAGCTTGGGTGAT TTGAGCCCTGAAGGTCAAGGCTGCAGTGAGCCGTGATCGTGCCACTGCACTCCAGCTTGGGTGAT T C HECTD4 Ensembl:ENSG00000173064 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1433295042 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24933081 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 27784 RMVar_ID_27784 Human_SNP_ID_516093161 A-to-I Human chr12 - 112289224 112289224 112289224 GTGGTGGTTCACACCTGTAGTCTCAGCTAGTAAGTAGCATGAGGTGGGAGGATCGCTTGAGCCCT GTGGTGGTTCACACCTGTAGTCTCAGCTAGTAGGTAGCATGAGGTGGGAGGATCGCTTGAGCCCT T C HECTD4 Ensembl:ENSG00000173064 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1489357696 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 27785 RMVar_ID_27785 Human_SNP_ID_516096050 A-to-I Human chr12 - 112300799 112300799 112300799 GCCAAGAAGTTCAAGACCAGCCTGAGCAACATAGTGGGATGCCACCTCTACAAAAATTTTTTTTA GCCAAGAAGTTCAAGACCAGCCTGAGCAACATCGTGGGATGCCACCTCTACAAAAATTTTTTTTA T G HECTD4 Ensembl:ENSG00000173064 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1030957551 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 27786 RMVar_ID_27786 Human_SNP_ID_516096698 A-to-I Human chr12 - 112303678 112303678 112303678 CCCAGCTAATTTTTGTGTTTTTTTGTAGAGACAGGGTTTCACCATGTTGCTTGGGCTGGCTTCGA CCCAGCTAATTTTTGTGTTTTTTTGTAGAGACTGGGTTTCACCATGTTGCTTGGGCTGGCTTCGA T A HECTD4 Ensembl:ENSG00000173064 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1453889745 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 27787 RMVar_ID_27787 Human_SNP_ID_516096699 A-to-I Human chr12 - 112303678 112303678 112303678 CCCAGCTAATTTTTGTGTTTTTTTGTAGAGACAGGGTTTCACCATGTTGCTTGGGCTGGCTTCGA CCCAGCTAATTTTTGTGTTTTTTTGTAGAGACGGGGTTTCACCATGTTGCTTGGGCTGGCTTCGA T C HECTD4 Ensembl:ENSG00000173064 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1453889745 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 27788 RMVar_ID_27788 Human_SNP_ID_516120675 A-to-I Human chr12 - 112405858 112405858 112405858 GACACCAGGAAGGTGAGATCTTCGACACAGAAAAAGAGGTAAGTTTCTACTTGTCATCTCCTGTG GACACCAGGAAGGTGAGATCTTCGACACAGAAGAAGAGGTAAGTTTCTACTTGTCATCTCCTGTG T C RPL6 Ensembl:ENSG00000089009 Protein coding exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs16942044 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_228515,Human_RBP_ID_753034,Human_RBP_ID_809707,Human_RBP_ID_876152,Human_RBP_ID_19059213,Human_RBP_ID_26322032 Human_Splice_Rec_1426999,Human_Splice_Rec_1427011 GWAS_ID_2799 RMVar_hsa_circ_64786,RMVar_hsa_circ_160251,RMVar_hsa_circ_104272,RMVar_hsa_circ_63484 27789 RMVar_ID_27789 Human_SNP_ID_516121240 A-to-I Human chr12 - 112407839 112407839 112407839 CCTGTAGTCCCAGCTGCTCTGGAGGCTGAGGCAGAAGAATCGCTTGAACCCGGGAGGCAGAGATT CCTGTAGTCCCAGCTGCTCTGGAGGCTGAGGCGGAAGAATCGCTTGAACCCGGGAGGCAGAGATT T C RPL6 Ensembl:ENSG00000089009 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1461211813 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24933464 RMVar_hsa_circ_94095,RMVar_hsa_circ_63484,RMVar_hsa_circ_160252 27790 RMVar_ID_27790 Human_SNP_ID_516126194 A-to-I Human chr12 + 112426987 112426987 112426987 TAGATAATGGCCGGGCGTGGTGGCTCACACCTATAATACCAGTACTTTGAGGGGCCGAGGCTGGC TAGATAATGGCCGGGCGTGGTGGCTCACACCTGTAATACCAGTACTTTGAGGGGCCGAGGCTGGC A G PTPN11 Ensembl:ENSG00000179295 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1254695867 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23539213,Human_RBP_ID_24933556 27791 RMVar_ID_27791 Human_SNP_ID_516134263 A-to-I Human chr12 + 112460748 112460748 112460748 CCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCAGAAGGTGGCAGTT CCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCGGGAGAATCGCTTGAACCCAGAAGGTGGCAGTT A G PTPN11 Ensembl:ENSG00000179295 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs948612588 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35502,RMVar_hsa_circ_358541,RMVar_hsa_circ_372737,RMVar_hsa_circ_329113,RMVar_hsa_circ_42422,RMVar_hsa_circ_36074,RMVar_hsa_circ_98846,RMVar_hsa_circ_160256,RMVar_hsa_circ_96056,RMVar_hsa_circ_82666,RMVar_hsa_circ_92056,RMVar_hsa_circ_80289,RMVar_hsa_circ_84249,RMVar_hsa_circ_160259,RMVar_hsa_circ_160261,RMVar_hsa_circ_160260,RMVar_hsa_circ_160257,RMVar_hsa_circ_160258,RMVar_hsa_circ_160266,RMVar_hsa_circ_123466,RMVar_hsa_circ_360119,RMVar_hsa_circ_333016,RMVar_hsa_circ_10648,RMVar_hsa_circ_40641,RMVar_hsa_circ_160267,RMVar_hsa_circ_367966 27792 RMVar_ID_27792 Human_SNP_ID_516140674 A-to-I Human chr12 + 112490452 112490452 112490452 CCTCAGCCTCCCAAGTAGCTGGGACTATAGGCATGCGCCACCACACCTAGCTAATTTTCGCATTT CCTCAGCCTCCCAAGTAGCTGGGACTATAGGCGTGCGCCACCACACCTAGCTAATTTTCGCATTT A G PTPN11 Ensembl:ENSG00000179295 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1025335890 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80289,RMVar_hsa_circ_160257,RMVar_hsa_circ_160266,RMVar_hsa_circ_123466,RMVar_hsa_circ_10648,RMVar_hsa_circ_318461 27793 RMVar_ID_27793 Human_SNP_ID_516141649 A-to-I Human chr12 + 112494829 112494829 112494829 TTATGATGGTTCGACTTATGATTTTTGATTTTATGATGGTTTGAGAGCAATACATCCATTCTGTT TTATGATGGTTCGACTTATGATTTTTGATTTTGTGATGGTTTGAGAGCAATACATCCATTCTGTT A G PTPN11 Ensembl:ENSG00000179295 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs746678128 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80289,RMVar_hsa_circ_160257,RMVar_hsa_circ_160266,RMVar_hsa_circ_123466,RMVar_hsa_circ_10648,RMVar_hsa_circ_318461 27794 RMVar_ID_27794 Human_SNP_ID_516141650 A-to-I Human chr12 + 112494829 112494829 112494829 TTATGATGGTTCGACTTATGATTTTTGATTTTATGATGGTTTGAGAGCAATACATCCATTCTGTT TTATGATGGTTCGACTTATGATTTTTGATTTTTTGATGGTTTGAGAGCAATACATCCATTCTGTT A T PTPN11 Ensembl:ENSG00000179295 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs746678128 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80289,RMVar_hsa_circ_160257,RMVar_hsa_circ_160266,RMVar_hsa_circ_123466,RMVar_hsa_circ_10648,RMVar_hsa_circ_318461 27795 RMVar_ID_27795 Human_SNP_ID_516141670 A-to-I Human chr12 + 112494912 112494912 112494912 ACTTTATTTTAAAATAGGGATTGTGAGATGATATTGCCCACGTGTAGGCTAATGTAAGTGTTCTG ACTTTATTTTAAAATAGGGATTGTGAGATGATGTTGCCCACGTGTAGGCTAATGTAAGTGTTCTG A G PTPN11 Ensembl:ENSG00000179295 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs374893695 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80289,RMVar_hsa_circ_160257,RMVar_hsa_circ_160266,RMVar_hsa_circ_123466,RMVar_hsa_circ_10648,RMVar_hsa_circ_318461 27796 RMVar_ID_27796 Human_SNP_ID_516141824 A-to-I Human chr12 + 112495702 112495702 112495702 GTCAAAAATGCATTTAATGCATCTAAACTACTAAACATCACAGCTTAGCCTAGCCTGCCTTGAAC GTCAAAAATGCATTTAATGCATCTAAACTACTGAACATCACAGCTTAGCCTAGCCTGCCTTGAAC A G PTPN11 Ensembl:ENSG00000179295 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs553914683 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80289,RMVar_hsa_circ_160257,RMVar_hsa_circ_160266,RMVar_hsa_circ_123466,RMVar_hsa_circ_10648,RMVar_hsa_circ_318461 27797 RMVar_ID_27797 Human_SNP_ID_516142265 A-to-I Human chr12 + 112498038 112498038 112498038 AGCTGGGCATGGTGGCTCACACCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCATGAGAATCGCT AGCTGGGCATGGTGGCTCACACCTGTAGTCCCGGCTACTTGGGAGGCTGAGGCATGAGAATCGCT A G PTPN11 Ensembl:ENSG00000179295 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs946154750 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80289,RMVar_hsa_circ_160257,RMVar_hsa_circ_160266,RMVar_hsa_circ_123466,RMVar_hsa_circ_10648,RMVar_hsa_circ_318461 27798 RMVar_ID_27798 Human_SNP_ID_516142613 A-to-I Human chr12 + 112499768 112499768 112499768 GGCCAAGAGTTTGAGACCAGTCTGGGCAACATAATGAGACCCCCTCTCTACAAAAAATAAAAAAA GGCCAAGAGTTTGAGACCAGTCTGGGCAACATGATGAGACCCCCTCTCTACAAAAAATAAAAAAA A G PTPN11 Ensembl:ENSG00000179295 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1411237625 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80289,RMVar_hsa_circ_160257,RMVar_hsa_circ_160266,RMVar_hsa_circ_123466,RMVar_hsa_circ_10648,RMVar_hsa_circ_318461 27799 RMVar_ID_27799 Human_SNP_ID_516142614 A-to-I Human chr12 + 112499768 112499768 112499768 GGCCAAGAGTTTGAGACCAGTCTGGGCAACATAATGAGACCCCCTCTCTACAAAAAATAAAAAAA GGCCAAGAGTTTGAGACCAGTCTGGGCAACATTATGAGACCCCCTCTCTACAAAAAATAAAAAAA A T PTPN11 Ensembl:ENSG00000179295 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1411237625 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80289,RMVar_hsa_circ_160257,RMVar_hsa_circ_160266,RMVar_hsa_circ_123466,RMVar_hsa_circ_10648,RMVar_hsa_circ_318461 27800 RMVar_ID_27800 Human_SNP_ID_516142716 A-to-I Human chr12 + 112500182 112500182 112500182 AGAGAATTGCTTGAACCTGGGAGGCAGAGGCTACAGTGAGCCGAGATCACACCACTGCACTCCAG AGAGAATTGCTTGAACCTGGGAGGCAGAGGCTGCAGTGAGCCGAGATCACACCACTGCACTCCAG A G PTPN11 Ensembl:ENSG00000179295 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7953069 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80289,RMVar_hsa_circ_160257,RMVar_hsa_circ_160266,RMVar_hsa_circ_123466,RMVar_hsa_circ_10648,RMVar_hsa_circ_318461 27801 RMVar_ID_27801 Human_SNP_ID_516142829 A-to-I Human chr12 + 112500666 112500666 112500666 CAGGCTGCAGTGCAGTGGCCTGATCTTGGCTCACTGCAACCTCCACCTCCCAGGTTCAAGCGATT CAGGCTGCAGTGCAGTGGCCTGATCTTGGCTCGCTGCAACCTCCACCTCCCAGGTTCAAGCGATT A G PTPN11 Ensembl:ENSG00000179295 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1315423838 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80289,RMVar_hsa_circ_160257,RMVar_hsa_circ_160266,RMVar_hsa_circ_123466,RMVar_hsa_circ_10648,RMVar_hsa_circ_318461 27802 RMVar_ID_27802 Human_SNP_ID_516142978 A-to-I Human chr12 + 112501514 112501514 112501514 GGGCATGGTGGTGGGCACCTGTAATCCCAGCTACTCAGGAGGCTGAGGCATGAAAATCGCTTGAA GGGCATGGTGGTGGGCACCTGTAATCCCAGCTCCTCAGGAGGCTGAGGCATGAAAATCGCTTGAA A C PTPN11 Ensembl:ENSG00000179295 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1566192009 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80289,RMVar_hsa_circ_160257,RMVar_hsa_circ_160266,RMVar_hsa_circ_123466,RMVar_hsa_circ_10648,RMVar_hsa_circ_318461 27803 RMVar_ID_27803 Human_SNP_ID_516245594 A-to-I Human chr12 + 112942433 112942433 112942433 GTAATCAAGCTTAGAAGTGTGTCTAGTGGGCCAGGCGCAGTGGCTCATGCCTGTAATCCCAGCTT GTAATCAAGCTTAGAAGTGTGTCTAGTGGGCCTGGCGCAGTGGCTCATGCCTGTAATCCCAGCTT A T OAS3 Ensembl:ENSG00000111331 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1356680924 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90179,RMVar_hsa_circ_79891,RMVar_hsa_circ_160279,RMVar_hsa_circ_160280 27804 RMVar_ID_27804 Human_SNP_ID_516245618 A-to-I Human chr12 + 112942525 112942525 112942525 GCCCAGGAGTTCAAGATCAGCCTTGGCAAAATAGCAAGATCTAGTCTCTACAAATAATAATAATT GCCCAGGAGTTCAAGATCAGCCTTGGCAAAATGGCAAGATCTAGTCTCTACAAATAATAATAATT A G OAS3 Ensembl:ENSG00000111331 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1137462 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90179,RMVar_hsa_circ_79891,RMVar_hsa_circ_160279,RMVar_hsa_circ_160280 27805 RMVar_ID_27805 Human_SNP_ID_516245739 A-to-I Human chr12 + 112943039 112943039 112943039 GGCTCACTGCAACCTCCGTCCTGGGTTCAAGCAATCCTCCCACCTCAGCCTCCCGAGTAGCTGGG GGCTCACTGCAACCTCCGTCCTGGGTTCAAGCCATCCTCCCACCTCAGCCTCCCGAGTAGCTGGG A C OAS3 Ensembl:ENSG00000111331 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs950009910 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90179,RMVar_hsa_circ_79891,RMVar_hsa_circ_160279,RMVar_hsa_circ_160280 27806 RMVar_ID_27806 Human_SNP_ID_516245740 A-to-I Human chr12 + 112943039 112943039 112943039 GGCTCACTGCAACCTCCGTCCTGGGTTCAAGCAATCCTCCCACCTCAGCCTCCCGAGTAGCTGGG GGCTCACTGCAACCTCCGTCCTGGGTTCAAGCGATCCTCCCACCTCAGCCTCCCGAGTAGCTGGG A G OAS3 Ensembl:ENSG00000111331 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs950009910 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90179,RMVar_hsa_circ_79891,RMVar_hsa_circ_160279,RMVar_hsa_circ_160280 27807 RMVar_ID_27807 Human_SNP_ID_516245795 A-to-I Human chr12 + 112943327 112943327 112943327 ACTTGACATGTTTTATCTCATCAATTCTTCACAACAAACTTATGAGGTCTGTACTGTTTCAGCTT ACTTGACATGTTTTATCTCATCAATTCTTCACGACAAACTTATGAGGTCTGTACTGTTTCAGCTT A G OAS3 Ensembl:ENSG00000111331 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs915792848 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90179,RMVar_hsa_circ_79891,RMVar_hsa_circ_160279,RMVar_hsa_circ_160280 27808 RMVar_ID_27808 Human_SNP_ID_516302257 A-to-I Human chr12 - 113165894 113165894 113165894 CCTGGCCCGCGTTGCTGATAACGCCCAGCAGCAGTATGTGCGCTCACGCCCGGCGCCCTCGCCTG CCTGGCCCGCGTTGCTGATAACGCCCAGCAGCGGTATGTGCGCTCACGCCCGGCGCCCTCGCCTG T C DDX54 Ensembl:ENSG00000123064 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs766916048 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4202336 Human_Splice_Rec_1428183,Human_Splice_Rec_1428221,Human_Splice_Rec_1428239 RMVar_hsa_circ_105766,RMVar_hsa_circ_373685,RMVar_hsa_circ_115891,RMVar_hsa_circ_111144,RMVar_hsa_circ_160306,RMVar_hsa_circ_160307,RMVar_hsa_circ_160308,RMVar_hsa_circ_160310,RMVar_hsa_circ_47947 27809 RMVar_ID_27809 Human_SNP_ID_516305612 A-to-I Human chr12 - 113178595 113178595 113178595 GAGGTTGCAGTGAGCCGAGATGGCATTACTGCACTCCAACATGGGCGACAGCGCGAGACTCCAAT GAGGTTGCAGTGAGCCGAGATGGCATTACTGCGCTCCAACATGGGCGACAGCGCGAGACTCCAAT T C DDX54 Ensembl:ENSG00000123064 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1324963656 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2127,RMVar_hsa_circ_373685,RMVar_hsa_circ_111144,RMVar_hsa_circ_160307,RMVar_hsa_circ_160308,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_160315,RMVar_hsa_circ_160316,RMVar_hsa_circ_160317,RMVar_hsa_circ_100572 27810 RMVar_ID_27810 Human_SNP_ID_516305613 A-to-I Human chr12 - 113178595 113178595 113178595 GAGGTTGCAGTGAGCCGAGATGGCATTACTGCACTCCAACATGGGCGACAGCGCGAGACTCCAAT GAGGTTGCAGTGAGCCGAGATGGCATTACTGCCCTCCAACATGGGCGACAGCGCGAGACTCCAAT T G DDX54 Ensembl:ENSG00000123064 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1324963656 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2127,RMVar_hsa_circ_373685,RMVar_hsa_circ_111144,RMVar_hsa_circ_160307,RMVar_hsa_circ_160308,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_160315,RMVar_hsa_circ_160316,RMVar_hsa_circ_160317,RMVar_hsa_circ_100572 27811 RMVar_ID_27811 Human_SNP_ID_516305639 A-to-I Human chr12 - 113178742 113178742 113178742 GGTCAGGAGTTTGAGACCAGCCTGACCAACATAGCAGAACCCTGTCTCTACTAAAAATACAAAAA GGTCAGGAGTTTGAGACCAGCCTGACCAACATGGCAGAACCCTGTCTCTACTAAAAATACAAAAA T C DDX54 Ensembl:ENSG00000123064 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1247622773 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2127,RMVar_hsa_circ_373685,RMVar_hsa_circ_111144,RMVar_hsa_circ_160307,RMVar_hsa_circ_160308,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_160315,RMVar_hsa_circ_160316,RMVar_hsa_circ_160317,RMVar_hsa_circ_100572 27812 RMVar_ID_27812 Human_SNP_ID_516318369 A-to-I Human chr12 + 113228373 113228373 113228373 CCCCACCTTTAATCACAGCACTTTGGGAGGCCAAGGCAGGAAGATCACTTGAGCCCAGTGACTTT CCCCACCTTTAATCACAGCACTTTGGGAGGCCGAGGCAGGAAGATCACTTGAGCCCAGTGACTTT A G TPCN1 Ensembl:ENSG00000186815 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1356623779 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47588,RMVar_hsa_circ_272643,RMVar_hsa_circ_160321 27813 RMVar_ID_27813 Human_SNP_ID_516330948 A-to-I Human chr12 + 113281000 113281000 113281000 TTCACATTCAGGCCTACAGCAATTTTAAGATTAAGAATCTAGATGTGTAAGACTGATTTCATCAA TTCACATTCAGGCCTACAGCAATTTTAAGATTGAGAATCTAGATGTGTAAGACTGATTTCATCAA A G TPCN1 Ensembl:ENSG00000186815 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs923013429 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11827919 RMVar_hsa_circ_86814,RMVar_hsa_circ_84130,RMVar_hsa_circ_116531,RMVar_hsa_circ_91686,RMVar_hsa_circ_160330,RMVar_hsa_circ_160331,RMVar_hsa_circ_160332,RMVar_hsa_circ_111472,RMVar_hsa_circ_30367,RMVar_hsa_circ_160334,RMVar_hsa_circ_160337,RMVar_hsa_circ_160333,RMVar_hsa_circ_335839,RMVar_hsa_circ_86234,RMVar_hsa_circ_160341,RMVar_hsa_circ_106688,RMVar_hsa_circ_160344,RMVar_hsa_circ_91768,RMVar_hsa_circ_160347,RMVar_hsa_circ_160346,RMVar_hsa_circ_375162,RMVar_hsa_circ_160348,RMVar_hsa_circ_123699 27814 RMVar_ID_27814 Human_SNP_ID_516330975 A-to-I Human chr12 + 113281069 113281069 113281069 ACACGTCTAGATTCTCAATCCTTTTTTTTTTGAGACAGAGTCTCATTCTGTCGCCCAGGCTAGCG ACACGTCTAGATTCTCAATCCTTTTTTTTTTGGGACAGAGTCTCATTCTGTCGCCCAGGCTAGCG A G TPCN1 Ensembl:ENSG00000186815 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1429405812 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11827920 RMVar_hsa_circ_86814,RMVar_hsa_circ_84130,RMVar_hsa_circ_116531,RMVar_hsa_circ_91686,RMVar_hsa_circ_160330,RMVar_hsa_circ_160331,RMVar_hsa_circ_160332,RMVar_hsa_circ_111472,RMVar_hsa_circ_30367,RMVar_hsa_circ_160334,RMVar_hsa_circ_160337,RMVar_hsa_circ_160333,RMVar_hsa_circ_335839,RMVar_hsa_circ_86234,RMVar_hsa_circ_160341,RMVar_hsa_circ_106688,RMVar_hsa_circ_160344,RMVar_hsa_circ_91768,RMVar_hsa_circ_160347,RMVar_hsa_circ_160346,RMVar_hsa_circ_375162,RMVar_hsa_circ_160348,RMVar_hsa_circ_123699 27815 RMVar_ID_27815 Human_SNP_ID_516331001 A-to-I Human chr12 + 113281170 113281170 113281170 CTAAGTGATTCTCCTGTCTCACTCACCTGAGTAGCTGGGATTACAGGTGTGTGCCACCACGCCCA CTAAGTGATTCTCCTGTCTCACTCACCTGAGTGGCTGGGATTACAGGTGTGTGCCACCACGCCCA A G TPCN1 Ensembl:ENSG00000186815 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1009428932 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86814,RMVar_hsa_circ_84130,RMVar_hsa_circ_116531,RMVar_hsa_circ_91686,RMVar_hsa_circ_160330,RMVar_hsa_circ_160331,RMVar_hsa_circ_160332,RMVar_hsa_circ_111472,RMVar_hsa_circ_30367,RMVar_hsa_circ_160334,RMVar_hsa_circ_160337,RMVar_hsa_circ_160333,RMVar_hsa_circ_335839,RMVar_hsa_circ_86234,RMVar_hsa_circ_160341,RMVar_hsa_circ_106688,RMVar_hsa_circ_160344,RMVar_hsa_circ_91768,RMVar_hsa_circ_160347,RMVar_hsa_circ_160346,RMVar_hsa_circ_375162,RMVar_hsa_circ_160348,RMVar_hsa_circ_123699 27816 RMVar_ID_27816 Human_SNP_ID_516331103 A-to-I Human chr12 + 113281704 113281704 113281704 GGGACCACAGGTGCATGCCACCACACCTGGCTAATTTTTTAATTTTTTGTAGAGACGGGGTAGCC GGGACCACAGGTGCATGCCACCACACCTGGCTGATTTTTTAATTTTTTGTAGAGACGGGGTAGCC A G TPCN1 Ensembl:ENSG00000186815 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs962850152 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11827924 RMVar_hsa_circ_86814,RMVar_hsa_circ_84130,RMVar_hsa_circ_116531,RMVar_hsa_circ_91686,RMVar_hsa_circ_160330,RMVar_hsa_circ_160331,RMVar_hsa_circ_160332,RMVar_hsa_circ_111472,RMVar_hsa_circ_30367,RMVar_hsa_circ_160334,RMVar_hsa_circ_160337,RMVar_hsa_circ_160333,RMVar_hsa_circ_335839,RMVar_hsa_circ_86234,RMVar_hsa_circ_160341,RMVar_hsa_circ_106688,RMVar_hsa_circ_160344,RMVar_hsa_circ_91768,RMVar_hsa_circ_160347,RMVar_hsa_circ_160346,RMVar_hsa_circ_375162,RMVar_hsa_circ_160348,RMVar_hsa_circ_123699 27817 RMVar_ID_27817 Human_SNP_ID_516331305 A-to-I Human chr12 + 113282361 113282361 113282361 TTGATCCACCTGCCTCGGCCTCCCAAAGTGCTAGGATTACAGGCATGAGCCACCGCATCCGGCCT TTGATCCACCTGCCTCGGCCTCCCAAAGTGCTCGGATTACAGGCATGAGCCACCGCATCCGGCCT A C TPCN1 Ensembl:ENSG00000186815 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1033825306 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86814,RMVar_hsa_circ_84130,RMVar_hsa_circ_116531,RMVar_hsa_circ_91686,RMVar_hsa_circ_160330,RMVar_hsa_circ_160331,RMVar_hsa_circ_160332,RMVar_hsa_circ_111472,RMVar_hsa_circ_30367,RMVar_hsa_circ_160334,RMVar_hsa_circ_160337,RMVar_hsa_circ_160333,RMVar_hsa_circ_335839,RMVar_hsa_circ_86234,RMVar_hsa_circ_160341,RMVar_hsa_circ_106688,RMVar_hsa_circ_160344,RMVar_hsa_circ_91768,RMVar_hsa_circ_160347,RMVar_hsa_circ_160346,RMVar_hsa_circ_375162,RMVar_hsa_circ_160348,RMVar_hsa_circ_123699 27818 RMVar_ID_27818 Human_SNP_ID_516331363 A-to-I Human chr12 + 113282566 113282566 113282566 GAGCCCAAGAGTTTGAGACCAGCCTGGGCAACATAGTGAGACCCCTGTCTCTACAAAAAAAAAAA GAGCCCAAGAGTTTGAGACCAGCCTGGGCAACGTAGTGAGACCCCTGTCTCTACAAAAAAAAAAA A G TPCN1 Ensembl:ENSG00000186815 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1488751890 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86814,RMVar_hsa_circ_84130,RMVar_hsa_circ_116531,RMVar_hsa_circ_91686,RMVar_hsa_circ_160330,RMVar_hsa_circ_160331,RMVar_hsa_circ_160332,RMVar_hsa_circ_111472,RMVar_hsa_circ_30367,RMVar_hsa_circ_160334,RMVar_hsa_circ_160337,RMVar_hsa_circ_160333,RMVar_hsa_circ_335839,RMVar_hsa_circ_86234,RMVar_hsa_circ_160341,RMVar_hsa_circ_106688,RMVar_hsa_circ_160344,RMVar_hsa_circ_91768,RMVar_hsa_circ_160347,RMVar_hsa_circ_160346,RMVar_hsa_circ_375162,RMVar_hsa_circ_160348,RMVar_hsa_circ_123699 27819 RMVar_ID_27819 Human_SNP_ID_516331435 A-to-I Human chr12 + 113282830 113282830 113282830 AATTAGGCCTGGGCATGGTGGCTTATGCCTGTAATCCCAACACTTTGGGAGGCCGAGGCGGGCAG AATTAGGCCTGGGCATGGTGGCTTATGCCTGTCATCCCAACACTTTGGGAGGCCGAGGCGGGCAG A C TPCN1 Ensembl:ENSG00000186815 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1319874340 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86814,RMVar_hsa_circ_84130,RMVar_hsa_circ_116531,RMVar_hsa_circ_91686,RMVar_hsa_circ_160330,RMVar_hsa_circ_160331,RMVar_hsa_circ_160332,RMVar_hsa_circ_111472,RMVar_hsa_circ_30367,RMVar_hsa_circ_160334,RMVar_hsa_circ_160337,RMVar_hsa_circ_160333,RMVar_hsa_circ_335839,RMVar_hsa_circ_86234,RMVar_hsa_circ_160341,RMVar_hsa_circ_106688,RMVar_hsa_circ_160344,RMVar_hsa_circ_91768,RMVar_hsa_circ_160347,RMVar_hsa_circ_160346,RMVar_hsa_circ_375162,RMVar_hsa_circ_160348,RMVar_hsa_circ_123699 27820 RMVar_ID_27820 Human_SNP_ID_516331461 A-to-I Human chr12 + 113282915 113282915 113282915 CGAGACCAGCCTGAGCAATGTGGTGAAACCCCATCTCTACCAAAAATAGAAAAAATTAGCCATGC CGAGACCAGCCTGAGCAATGTGGTGAAACCCCGTCTCTACCAAAAATAGAAAAAATTAGCCATGC A G TPCN1 Ensembl:ENSG00000186815 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1014394018 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86814,RMVar_hsa_circ_84130,RMVar_hsa_circ_116531,RMVar_hsa_circ_91686,RMVar_hsa_circ_160330,RMVar_hsa_circ_160331,RMVar_hsa_circ_160332,RMVar_hsa_circ_111472,RMVar_hsa_circ_30367,RMVar_hsa_circ_160334,RMVar_hsa_circ_160337,RMVar_hsa_circ_160333,RMVar_hsa_circ_335839,RMVar_hsa_circ_86234,RMVar_hsa_circ_160341,RMVar_hsa_circ_106688,RMVar_hsa_circ_160344,RMVar_hsa_circ_91768,RMVar_hsa_circ_160347,RMVar_hsa_circ_160346,RMVar_hsa_circ_375162,RMVar_hsa_circ_160348,RMVar_hsa_circ_123699 27821 RMVar_ID_27821 Human_SNP_ID_516331476 A-to-I Human chr12 + 113282997 113282997 113282997 TACTTGGGAGGCTGAGGCAGGAGGATCACTTGATCCTGAGAGGCAGAGGTTGCAGTGAGTTGTGA TACTTGGGAGGCTGAGGCAGGAGGATCACTTGTTCCTGAGAGGCAGAGGTTGCAGTGAGTTGTGA A T TPCN1 Ensembl:ENSG00000186815 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs748811151 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86814,RMVar_hsa_circ_84130,RMVar_hsa_circ_116531,RMVar_hsa_circ_91686,RMVar_hsa_circ_160330,RMVar_hsa_circ_160331,RMVar_hsa_circ_160332,RMVar_hsa_circ_111472,RMVar_hsa_circ_30367,RMVar_hsa_circ_160334,RMVar_hsa_circ_160337,RMVar_hsa_circ_160333,RMVar_hsa_circ_335839,RMVar_hsa_circ_86234,RMVar_hsa_circ_160341,RMVar_hsa_circ_106688,RMVar_hsa_circ_160344,RMVar_hsa_circ_91768,RMVar_hsa_circ_160347,RMVar_hsa_circ_160346,RMVar_hsa_circ_375162,RMVar_hsa_circ_160348,RMVar_hsa_circ_123699 27822 RMVar_ID_27822 Human_SNP_ID_516344281 A-to-I Human chr12 - 113331349 113331349 113331349 ACAGTCTCACTCTATACCCAGGCTGGAGTGCAATGGCACGATCTCAGCTCACTGCAACCTCCACC ACAGTCTCACTCTATACCCAGGCTGGAGTGCAGTGGCACGATCTCAGCTCACTGCAACCTCCACC T C SLC8B1 Ensembl:ENSG00000089060 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1161621210 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86598,RMVar_hsa_circ_87996,RMVar_hsa_circ_77738,RMVar_hsa_circ_160360,RMVar_hsa_circ_120051,RMVar_hsa_circ_160362,RMVar_hsa_circ_160363,RMVar_hsa_circ_160365 27823 RMVar_ID_27823 Human_SNP_ID_516344283 A-to-I Human chr12 - 113331373 113331373 113331373 TTTTTTTTTTTTTTTTTTTCGAGAACAGTCTCACTCTATACCCAGGCTGGAGTGCAATGGCACGA TTTTTTTTTTTTTTTTTTTCGAGAACAGTCTCGCTCTATACCCAGGCTGGAGTGCAATGGCACGA T C SLC8B1 Ensembl:ENSG00000089060 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1421070179 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86598,RMVar_hsa_circ_87996,RMVar_hsa_circ_77738,RMVar_hsa_circ_160360,RMVar_hsa_circ_120051,RMVar_hsa_circ_160362,RMVar_hsa_circ_160363,RMVar_hsa_circ_160365 27824 RMVar_ID_27824 Human_SNP_ID_516344501 A-to-I Human chr12 - 113332332 113332332 113332332 GTGAGGTGGATGTTGCAGTGAGCCAGGATTGTACCACTGCACTCCAGCCTGGGCGGCGAAGCAAG GTGAGGTGGATGTTGCAGTGAGCCAGGATTGTTCCACTGCACTCCAGCCTGGGCGGCGAAGCAAG T A SLC8B1 Ensembl:ENSG00000089060 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs760132598 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86598,RMVar_hsa_circ_87996,RMVar_hsa_circ_77738,RMVar_hsa_circ_160360,RMVar_hsa_circ_120051,RMVar_hsa_circ_160362,RMVar_hsa_circ_160363,RMVar_hsa_circ_160365 27825 RMVar_ID_27825 Human_SNP_ID_516352428 A-to-I Human chr12 + 113363331 113363331 113363331 GGTGGTGCGTGCCTGTAGTTCCAGCTACTCAGAAGCTGAGACGGGAGGACTGCTTGAGTCCAGGT GGTGGTGCGTGCCTGTAGTTCCAGCTACTCAGGAGCTGAGACGGGAGGACTGCTTGAGTCCAGGT A G PLBD2 Ensembl:ENSG00000151176 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1177556608 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81123,RMVar_hsa_circ_123354,RMVar_hsa_circ_160368,RMVar_hsa_circ_160369 27826 RMVar_ID_27826 Human_SNP_ID_516355740 A-to-I Human chr12 + 113376742 113376742 113376742 GGGAATTCGAAGCAGGAGGATTGCTTGAGCCCAGGAGGTTGAGGCTGCAGTGAACAGTGATCACG GGGAATTCGAAGCAGGAGGATTGCTTGAGCCCGGGAGGTTGAGGCTGCAGTGAACAGTGATCACG A G PLBD2 Ensembl:ENSG00000151176 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903503995 Functional Loss SNV dbSNP153 33..33 33 - - - 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_160377 27827 RMVar_ID_27827 Human_SNP_ID_516359370 A-to-I Human chr12 + 113390111 113390111 113390111 ATGAGATCAGACAGGGAGGGATCCTTTTTTGTATTGGTCTGTATACCACAGCATGGCTTACGAAG ATGAGATCAGACAGGGAGGGATCCTTTTTTGTGTTGGTCTGTATACCACAGCATGGCTTACGAAG A G PLBD2 Ensembl:ENSG00000151176 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs112693280 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_194948,Human_RBP_ID_259918,Human_RBP_ID_2306594,Human_RBP_ID_6137122,Human_RBP_ID_11828182,Human_RBP_ID_17242995,Human_RBP_ID_17560926,Human_RBP_ID_17650482,Human_RBP_ID_22369787,Human_RBP_ID_22436710,Human_RBP_ID_24529983,Human_RBP_ID_24934362,Human_RBP_ID_26412187,Human_RBP_ID_26806117 27828 RMVar_ID_27828 Human_SNP_ID_516359371 A-to-I Human chr12 + 113390111 113390111 113390111 ATGAGATCAGACAGGGAGGGATCCTTTTTTGTATTGGTCTGTATACCACAGCATGGCTTACGAAG ATGAGATCAGACAGGGAGGGATCCTTTTTTGTTTTGGTCTGTATACCACAGCATGGCTTACGAAG A T PLBD2 Ensembl:ENSG00000151176 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs112693280 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_194948,Human_RBP_ID_259918,Human_RBP_ID_2306594,Human_RBP_ID_6137122,Human_RBP_ID_11828182,Human_RBP_ID_17242995,Human_RBP_ID_17560926,Human_RBP_ID_17650482,Human_RBP_ID_22369787,Human_RBP_ID_22436710,Human_RBP_ID_24529983,Human_RBP_ID_24934362,Human_RBP_ID_26412187,Human_RBP_ID_26806117 27829 RMVar_ID_27829 Human_SNP_ID_516359627 A-to-I Human chr12 + 113391134 113391134 113391134 ACCACCAAGACCTTCCTAAGCCATATTGTGGTATACAGACAGATACAAAAAAAAAGGCTCTCTCC ACCACCAAGACCTTCCTAAGCCATATTGTGGTGTACAGACAGATACAAAAAAAAAGGCTCTCTCC A G PLBD2 Ensembl:ENSG00000151176 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs746466699 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_194494,Human_RBP_ID_259933,Human_RBP_ID_1267185,Human_RBP_ID_3418483,Human_RBP_ID_17075372,Human_RBP_ID_17561286,Human_RBP_ID_22369790,Human_RBP_ID_24530000,Human_RBP_ID_26421671,Human_RBP_ID_26755648,Human_RBP_ID_26807139,Human_RBP_ID_27418657 27830 RMVar_ID_27830 Human_SNP_ID_516359633 A-to-I Human chr12 + 113391148 113391147 113391148 CCTAAGCCATATTGTGGTATACAGACAGATACAAAAAAAAAGGCTCTCTCCCTGTCTGATCTCAT CCTAAGCCATATTGTGGTATACAGACAGATAC_AAAAAAAAGGCTCTCTCCCTGTCTGATCTCAT CA C PLBD2 Ensembl:ENSG00000151176 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs201259647 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_194985,Human_RBP_ID_259934,Human_RBP_ID_2306617,Human_RBP_ID_17075372,Human_RBP_ID_17561286,Human_RBP_ID_22369790,Human_RBP_ID_24530000,Human_RBP_ID_26412228,Human_RBP_ID_26755649 27831 RMVar_ID_27831 Human_SNP_ID_516360940 A-to-I Human chr12 - 113396053 113396053 113396053 CTCTTGTTGCCCAAGCTGGAGTGCAATGGTACAATCTCAGCTCACCGCAACCTCTGCCTCCCAAG CTCTTGTTGCCCAAGCTGGAGTGCAATGGTACGATCTCAGCTCACCGCAACCTCTGCCTCCCAAG T C SDS Ensembl:ENSG00000135094 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1331575677 Functional Loss SNV dbSNP153 33..33 33 - - - 27832 RMVar_ID_27832 Human_SNP_ID_516368730 A-to-I Human chr12 + 113425846 113425846 113425846 CCCGTCTCTACAAAAAATACAAAAAATTAATCAGGCGTGGTGACGTGTGCCTGTGGTCCCAGTTA CCCGTCTCTACAAAAAATACAAAAAATTAATCTGGCGTGGTGACGTGTGCCTGTGGTCCCAGTTA A T SDSL Ensembl:ENSG00000139410 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs531848476 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_160385,RMVar_hsa_circ_101937 27833 RMVar_ID_27833 Human_SNP_ID_516469508 A-to-I Human chr12 - 113810103 113810103 113810103 CAGTCTTGCTCCCTCACCCACGCTGGAGTGCAATGGCACGATCTCGGCTCGCTGAAACCTCTGCC CAGTCTTGCTCCCTCACCCACGCTGGAGTGCAGTGGCACGATCTCGGCTCGCTGAAACCTCTGCC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1214478350 Functional Loss SNV dbSNP153 33..33 33 - - - 27834 RMVar_ID_27834 Human_SNP_ID_516470225 A-to-I Human chr12 - 113813095 113813092 113813095 GCTGCCTCGGCACATGTGCTGAGTAAAACTTTATTGACAAGACCAGGCAACAGTAGCAGGAAAAA GCTGCCTCGGCACATGTGCTGAGTAAAACTTT___GACAAGACCAGGCAACAGTAGCAGGAAAAA CAAT C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1326538872 Functional Loss DEL dbSNP153 33..35 33 - - - 27835 RMVar_ID_27835 Human_SNP_ID_516470323 A-to-I Human chr12 - 113813454 113813452 113813454 GTAGTAAAGAAGCGACGTGAATGATCAAAATCAGGGGTTGGCAAACCATGGCCCTCTTTTTTTTT GTAGTAAAGAAGCGACGTGAATGATCAAAATC__GGGTTGGCAAACCATGGCCCTCTTTTTTTTT CCT C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs139857182 Functional Loss DEL dbSNP153 33..34 33 - - - 27836 RMVar_ID_27836 Human_SNP_ID_516470544 A-to-I Human chr12 - 113814408 113814408 113814408 GGCTCACTGCAGCCCCTGCCTCTCTGGGTTCAAGCAGTCCTCCCACTTCATCCTCCCAAGTAGCT GGCTCACTGCAGCCCCTGCCTCTCTGGGTTCACGCAGTCCTCCCACTTCATCCTCCCAAGTAGCT T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1394912526 Functional Loss SNV dbSNP153 33..33 33 - - - 27837 RMVar_ID_27837 Human_SNP_ID_516471552 A-to-I Human chr12 - 113818049 113818049 113818049 TAATTTTGTATTTTTCATAGAGACTGGGTTTCACCATGTAGACCAGGCTGGTCTCGAATTCCTGA TAATTTTGTATTTTTCATAGAGACTGGGTTTCCCCATGTAGACCAGGCTGGTCTCGAATTCCTGA T G RBM19 Ensembl:ENSG00000122965 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1416797872 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11828348 RMVar_hsa_circ_116265,RMVar_hsa_circ_160388 27838 RMVar_ID_27838 Human_SNP_ID_516507636 A-to-I Human chr12 - 113959361 113959361 113959361 TACAGAGTTCCAGGAGTTTCTGTCAGTTCATCAGAGGCGGGCGCAGGCAGCCACTTGGGCGAATG TACAGAGTTCCAGGAGTTTCTGTCAGTTCATCGGAGGCGGGCGCAGGCAGCCACTTGGGCGAATG T C RBM19 Ensembl:ENSG00000122965 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1244833343 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_34432,Human_RBP_ID_873890,Human_RBP_ID_3943558,Human_RBP_ID_5462347,Human_RBP_ID_5521771,Human_RBP_ID_9365623,Human_RBP_ID_18469246,Human_RBP_ID_18976243,Human_RBP_ID_26321021,Human_RBP_ID_26768421,Human_RBP_ID_27806043 Human_Splice_Rec_1429224,Human_Splice_Rec_1429272,Human_Splice_Rec_1429320 RMVar_hsa_circ_18309,RMVar_hsa_circ_106154,RMVar_hsa_circ_116265,RMVar_hsa_circ_160388,RMVar_hsa_circ_87612,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_328365 27839 RMVar_ID_27839 Human_SNP_ID_516672476 A-to-I Human chr12 - 114588420 114588420 114588420 TCAAGTTGCCTCTTTTTGCTACTTCATGCAATAGATTGTCAATGGATTCTGCCTGCTCGGCCACA TCAAGTTGCCTCTTTTTGCTACTTCATGCAATGGATTGTCAATGGATTCTGCCTGCTCGGCCACA T C HSALNG0094220 RNACentral:URS0000EA1A7F lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878875562 Functional Loss SNV dbSNP153 33..33 33 - - - 27840 RMVar_ID_27840 Human_SNP_ID_516672478 A-to-I Human chr12 - 114588432 114588432 114588432 CTCGCAACCAACTCAAGTTGCCTCTTTTTGCTACTTCATGCAATAGATTGTCAATGGATTCTGCC CTCGCAACCAACTCAAGTTGCCTCTTTTTGCTGCTTCATGCAATAGATTGTCAATGGATTCTGCC T C HSALNG0094220 RNACentral:URS0000EA1A7F lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879204202 Functional Loss SNV dbSNP153 33..33 33 - - - 27841 RMVar_ID_27841 Human_SNP_ID_516672483 A-to-I Human chr12 - 114588454 114588454 114588454 CCCACTCGGTTGTCCAAACACTCTCGCAACCAACTCAAGTTGCCTCTTTTTGCTACTTCATGCAA CCCACTCGGTTGTCCAAACACTCTCGCAACCAGCTCAAGTTGCCTCTTTTTGCTACTTCATGCAA T C HSALNG0094220 RNACentral:URS0000EA1A7F lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1156385213 Functional Loss SNV dbSNP153 33..33 33 - - - 27842 RMVar_ID_27842 Human_SNP_ID_516724170 A-to-I Human chr12 + 114775234 114775234 114775234 TTAAGTCCTGACCAGTCTTGGTGGCCATGTCTATACTCCCAGCACTTTGGGAGGCCGAGGCAGAA TTAAGTCCTGACCAGTCTTGGTGGCCATGTCTGTACTCCCAGCACTTTGGGAGGCCGAGGCAGAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs866429768 Functional Loss SNV dbSNP153 33..33 33 - - - 27843 RMVar_ID_27843 Human_SNP_ID_517039727 A-to-I Human chr12 - 116062293 116062293 116062293 AAAATATTAGCTGGTCTTGGTGATTCATGCCTATGGTCCCAGCTACTCTGTAGGTTGAGGTGGAA AAAATATTAGCTGGTCTTGGTGATTCATGCCTGTGGTCCCAGCTACTCTGTAGGTTGAGGTGGAA T C MED13L Ensembl:ENSG00000123066 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1473963033 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125519,RMVar_hsa_circ_91405,RMVar_hsa_circ_160412,RMVar_hsa_circ_370183,RMVar_hsa_circ_124702,RMVar_hsa_circ_160416,RMVar_hsa_circ_160417,RMVar_hsa_circ_160418,RMVar_hsa_circ_83482,RMVar_hsa_circ_116037,RMVar_hsa_circ_101133,RMVar_hsa_circ_160421,RMVar_hsa_circ_160422,RMVar_hsa_circ_117846,RMVar_hsa_circ_160425,RMVar_hsa_circ_160426,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_127121,RMVar_hsa_circ_160432,RMVar_hsa_circ_160434,RMVar_hsa_circ_78417,RMVar_hsa_circ_371921,RMVar_hsa_circ_160438,RMVar_hsa_circ_91541,RMVar_hsa_circ_160440,RMVar_hsa_circ_119277,RMVar_hsa_circ_99379,RMVar_hsa_circ_160442,RMVar_hsa_circ_160444,RMVar_hsa_circ_108776,RMVar_hsa_circ_160443,RMVar_hsa_circ_100853,RMVar_hsa_circ_63403,RMVar_hsa_circ_43844,RMVar_hsa_circ_97562,RMVar_hsa_circ_160446,RMVar_hsa_circ_112235,RMVar_hsa_circ_128059,RMVar_hsa_circ_160447,RMVar_hsa_circ_160449,RMVar_hsa_circ_105008,RMVar_hsa_circ_160448,RMVar_hsa_circ_160452,RMVar_hsa_circ_76796,RMVar_hsa_circ_160451 27844 RMVar_ID_27844 Human_SNP_ID_517042693 A-to-I Human chr12 - 116074381 116074377 116074381 AGTTTTTTGTTGTTGTTTTGAGGCAGAGTCTCACTCTGTCGCCCAGGCTAGAGTGCAGTGGCAAG AGTTTTTTGTTGTTGTTTTGAGGCAGAGTCTC____TGTCGCCCAGGCTAGAGTGCAGTGGCAAG AGAGT A MED13L Ensembl:ENSG00000123066 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1379170809 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_125519,RMVar_hsa_circ_91405,RMVar_hsa_circ_160412,RMVar_hsa_circ_370183,RMVar_hsa_circ_124702,RMVar_hsa_circ_160416,RMVar_hsa_circ_160417,RMVar_hsa_circ_160418,RMVar_hsa_circ_83482,RMVar_hsa_circ_116037,RMVar_hsa_circ_101133,RMVar_hsa_circ_160421,RMVar_hsa_circ_160422,RMVar_hsa_circ_117846,RMVar_hsa_circ_160425,RMVar_hsa_circ_160426,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_127121,RMVar_hsa_circ_160432,RMVar_hsa_circ_160434,RMVar_hsa_circ_78417,RMVar_hsa_circ_371921,RMVar_hsa_circ_160438,RMVar_hsa_circ_91541,RMVar_hsa_circ_160440,RMVar_hsa_circ_119277,RMVar_hsa_circ_99379,RMVar_hsa_circ_160442,RMVar_hsa_circ_160444,RMVar_hsa_circ_108776,RMVar_hsa_circ_160443,RMVar_hsa_circ_100853,RMVar_hsa_circ_63403,RMVar_hsa_circ_43844,RMVar_hsa_circ_97562,RMVar_hsa_circ_160446,RMVar_hsa_circ_112235,RMVar_hsa_circ_128059,RMVar_hsa_circ_160447,RMVar_hsa_circ_160449,RMVar_hsa_circ_105008,RMVar_hsa_circ_160448,RMVar_hsa_circ_160452,RMVar_hsa_circ_76796,RMVar_hsa_circ_160451 27845 RMVar_ID_27845 Human_SNP_ID_517049799 A-to-I Human chr12 - 116102850 116102850 116102850 AGGCGTGGTGGGGCGCGTCTGTAATCCCGGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAA AGGCGTGGTGGGGCGCGTCTGTAATCCCGGCTGCTCAGGAGGCTGAGGCAGGAGAATCGCTTGAA T C MED13L Ensembl:ENSG00000123066 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232565637 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125519,RMVar_hsa_circ_91405,RMVar_hsa_circ_160412,RMVar_hsa_circ_370183,RMVar_hsa_circ_160417,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_119199,RMVar_hsa_circ_160431,RMVar_hsa_circ_127121,RMVar_hsa_circ_160432,RMVar_hsa_circ_160434,RMVar_hsa_circ_78417,RMVar_hsa_circ_371921,RMVar_hsa_circ_160438,RMVar_hsa_circ_91541,RMVar_hsa_circ_160440,RMVar_hsa_circ_119277,RMVar_hsa_circ_99379,RMVar_hsa_circ_160442,RMVar_hsa_circ_160443,RMVar_hsa_circ_100853,RMVar_hsa_circ_63403,RMVar_hsa_circ_97562,RMVar_hsa_circ_160446,RMVar_hsa_circ_112235,RMVar_hsa_circ_128059,RMVar_hsa_circ_160447,RMVar_hsa_circ_160449,RMVar_hsa_circ_105008,RMVar_hsa_circ_160448,RMVar_hsa_circ_160452,RMVar_hsa_circ_76796,RMVar_hsa_circ_160451,RMVar_hsa_circ_273208,RMVar_hsa_circ_286545,RMVar_hsa_circ_119391,RMVar_hsa_circ_160454,RMVar_hsa_circ_160455,RMVar_hsa_circ_160453 27846 RMVar_ID_27846 Human_SNP_ID_517063234 A-to-I Human chr12 - 116155340 116155340 116155340 TGGCTCACTGCAGTCTGGAACCTCTGGGCTCAAGCAATCCTCCCACCTCAGTTTCCCAAGTAGCT TGGCTCACTGCAGTCTGGAACCTCTGGGCTCAGGCAATCCTCCCACCTCAGTTTCCCAAGTAGCT T C MED13L Ensembl:ENSG00000123066 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909345956 Functional Loss SNV dbSNP153 33..33 33 - - - 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 27847 RMVar_ID_27847 Human_SNP_ID_517066747 A-to-I Human chr12 - 116169965 116169965 116169965 CTGCTCAGACAGGAGTGCAGTGGCGTGATCGTAGCCCACCGCAGCTTTGAACTACTGGGCTCAAG CTGCTCAGACAGGAGTGCAGTGGCGTGATCGTGGCCCACCGCAGCTTTGAACTACTGGGCTCAAG T C MED13L Ensembl:ENSG00000123066 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs773128516 Functional Loss SNV dbSNP153 33..33 33 - - - 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 27848 RMVar_ID_27848 Human_SNP_ID_517072325 A-to-I Human chr12 - 116192943 116192943 116192943 TATTTTTAATAGAGACGCGGTTTCACCGTGTTAGCCAGGATGGTCTTGATTTCCTGACCTGGTGA TATTTTTAATAGAGACGCGGTTTCACCGTGTTGGCCAGGATGGTCTTGATTTCCTGACCTGGTGA T C MED13L Ensembl:ENSG00000123066 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1419761571 Functional Loss SNV dbSNP153 33..33 33 - - - 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 27849 RMVar_ID_27849 Human_SNP_ID_517075781 A-to-I Human chr12 - 116207273 116207273 116207273 GAAAAAGCAAGGAACGGTGGCTCACATGTGTAATCCCAGCATTTTGGGAGGGTGAGGCAGGAGAA GAAAAAGCAAGGAACGGTGGCTCACATGTGTATTCCCAGCATTTTGGGAGGGTGAGGCAGGAGAA T A MED13L Ensembl:ENSG00000123066 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1345605256 Functional Loss SNV dbSNP153 33..33 33 - - - 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_99152,RMVar_hsa_circ_160454,RMVar_hsa_circ_160455,RMVar_hsa_circ_352987,RMVar_hsa_circ_160456 27850 RMVar_ID_27850 Human_SNP_ID_517078853 A-to-I Human chr12 - 116220436 116220436 116220436 CCTCGGCCTCCCAAAGTGTTGGGATTATAGGCATGAGTCACCACGTCCGGCCCTATGTTCTCTTT CCTCGGCCTCCCAAAGTGTTGGGATTATAGGCCTGAGTCACCACGTCCGGCCCTATGTTCTCTTT T G MED13L Ensembl:ENSG00000123066 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1206597370 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23156009,Human_RBP_ID_25019399 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_99152,RMVar_hsa_circ_160454,RMVar_hsa_circ_160455,RMVar_hsa_circ_352987,RMVar_hsa_circ_160456 27851 RMVar_ID_27851 Human_SNP_ID_517078880 A-to-I Human chr12 - 116220536 116220536 116220536 CACCACCATGCCTGGCAAATTTTTGTATTTTTAGTAGAGATGGGGTTTCGCCATAATGGCCAGGC CACCACCATGCCTGGCAAATTTTTGTATTTTTGGTAGAGATGGGGTTTCGCCATAATGGCCAGGC T C MED13L Ensembl:ENSG00000123066 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1461403367 Functional Loss SNV dbSNP153 33..33 33 - - - 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_99152,RMVar_hsa_circ_160454,RMVar_hsa_circ_160455,RMVar_hsa_circ_352987,RMVar_hsa_circ_160456 27852 RMVar_ID_27852 Human_SNP_ID_517081746 A-to-I Human chr12 - 116232904 116232904 116232904 TTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGTTGATCTCAAACTCCCAACCT TTTTGTATTTTTAGTAGAGATGGGGTTTCACCGTGTTGGCCAGGTTGATCTCAAACTCCCAACCT T C MED13L Ensembl:ENSG00000123066 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs963198973 Functional Loss SNV dbSNP153 33..33 33 - - - 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_115620,RMVar_hsa_circ_99152,RMVar_hsa_circ_160454,RMVar_hsa_circ_160455,RMVar_hsa_circ_352987,RMVar_hsa_circ_120502,RMVar_hsa_circ_125679,RMVar_hsa_circ_160456,RMVar_hsa_circ_160457,RMVar_hsa_circ_160458,RMVar_hsa_circ_118594,RMVar_hsa_circ_160460,RMVar_hsa_circ_106063,RMVar_hsa_circ_160461,RMVar_hsa_circ_160459 27853 RMVar_ID_27853 Human_SNP_ID_517082201 A-to-I Human chr12 - 116234826 116234826 116234826 AAACCCTGTGTTTACAAAAAATAAAAAAAAAAAATTAGCCAGGTGTGGTGACGTGCACCTGTAAT AAACCCTGTGTTTACAAAAAATAAAAAAAAAATATTAGCCAGGTGTGGTGACGTGCACCTGTAAT T A MED13L Ensembl:ENSG00000123066 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1200314136 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9666002 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_115620,RMVar_hsa_circ_99152,RMVar_hsa_circ_160454,RMVar_hsa_circ_160455,RMVar_hsa_circ_352987,RMVar_hsa_circ_120502,RMVar_hsa_circ_125679,RMVar_hsa_circ_160456,RMVar_hsa_circ_160457,RMVar_hsa_circ_160458,RMVar_hsa_circ_118594,RMVar_hsa_circ_160460,RMVar_hsa_circ_106063,RMVar_hsa_circ_160461,RMVar_hsa_circ_160459 27854 RMVar_ID_27854 Human_SNP_ID_517082202 A-to-I Human chr12 - 116234832 116234832 116234832 ATGGTGAAACCCTGTGTTTACAAAAAATAAAAAAAAAAAATTAGCCAGGTGTGGTGACGTGCACC ATGGTGAAACCCTGTGTTTACAAAAAATAAAAGAAAAAAATTAGCCAGGTGTGGTGACGTGCACC T C MED13L Ensembl:ENSG00000123066 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1381542572 Functional Loss SNV dbSNP153 33..33 33 - - - 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_115620,RMVar_hsa_circ_99152,RMVar_hsa_circ_160454,RMVar_hsa_circ_160455,RMVar_hsa_circ_352987,RMVar_hsa_circ_120502,RMVar_hsa_circ_125679,RMVar_hsa_circ_160456,RMVar_hsa_circ_160457,RMVar_hsa_circ_160458,RMVar_hsa_circ_118594,RMVar_hsa_circ_160460,RMVar_hsa_circ_106063,RMVar_hsa_circ_160461,RMVar_hsa_circ_160459 27855 RMVar_ID_27855 Human_SNP_ID_517203380 A-to-I Human chr12 - 116711378 116711378 116711378 GGCGCCCGCCACCGTGCCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCGTGTTAG GGCGCCCGCCACCGTGCCCAGCTAATTTTTGTGTTTTTAGTAGAGACGGGGTTTCACCGTGTTAG T C C12orf49 Ensembl:ENSG00000111412 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs532886248 Functional Loss SNV dbSNP153 33..33 33 - - - 27856 RMVar_ID_27856 Human_SNP_ID_517204130 A-to-I Human chr12 - 116714577 116714577 116714577 GTTGGCCAGGCTGGTCACGGACTCCTGACCTCAGATGATCTGCCCGCCTGAGCCTCCGAAAGTGC GTTGGCCAGGCTGGTCACGGACTCCTGACCTCGGATGATCTGCCCGCCTGAGCCTCCGAAAGTGC T C C12orf49 Ensembl:ENSG00000111412 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049260489 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_411517,Human_RBP_ID_6139383,Human_RBP_ID_11833726 27857 RMVar_ID_27857 Human_SNP_ID_517204138 A-to-I Human chr12 - 116714628 116714628 116714628 ACCACACCCAGCTAAGTTTTTGTACTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGG ACCACACCCAGCTAAGTTTTTGTACTTTTAGTGGAGACGGGGTTTCACCATGTTGGCCAGGCTGG T C C12orf49 Ensembl:ENSG00000111412 Protein coding 3'UTR GSE38233;GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;ASD brains,cerebellum;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,30559470,31158229 RNA-Seq:(High) rs865849908 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4203128 27858 RMVar_ID_27858 Human_SNP_ID_517225771 A-to-I Human chr12 + 116802005 116802005 116802005 CACCATGCCCAGCTAATTTTTGTATTTGTAGCAGAGATGGAGTTTCGCCATGTTGGCCAGGCTGG CACCATGCCCAGCTAATTTTTGTATTTGTAGCGGAGATGGAGTTTCGCCATGTTGGCCAGGCTGG A G RNFT2 Ensembl:ENSG00000135119 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1156529516 Functional Loss SNV dbSNP153 33..33 33 - - - 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 27859 RMVar_ID_27859 Human_SNP_ID_517236067 A-to-I Human chr12 + 116843407 116843407 116843407 CGAGCTACTCAGGAGGCTGAGGTGGGAGGATCACTCGAGCCCCAAAAGGTCGAGGCTGCAGTGAG CGAGCTACTCAGGAGGCTGAGGTGGGAGGATCGCTCGAGCCCCAAAAGGTCGAGGCTGCAGTGAG A G RNFT2 Ensembl:ENSG00000135119 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1344292555 Functional Loss SNV dbSNP153 33..33 33 - - - 27860 RMVar_ID_27860 Human_SNP_ID_517238345 A-to-I Human chr12 + 116851524 116851523 116851524 ATTTTGGGAGGCTGAAGCAGGCGGGTCACCTGAGGTCAAGAGTTCAAGACTAGCCTGGCCAACAT ATTTTGGGAGGCTGAAGCAGGCGGGTCACCTG_GGTCAAGAGTTCAAGACTAGCCTGGCCAACAT GA G RNFT2 Ensembl:ENSG00000135119 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1250271059 Functional Loss DEL dbSNP153 33..33 33 - - - 27861 RMVar_ID_27861 Human_SNP_ID_517238403 A-to-I Human chr12 + 116851686 116851686 116851686 CTGCTTGAACTCGGGAGGTGAAAGTTGCAGTGAGCCGAGATTGCACCACAGCACTCCAACCTGGG CTGCTTGAACTCGGGAGGTGAAAGTTGCAGTGGGCCGAGATTGCACCACAGCACTCCAACCTGGG A G RNFT2 Ensembl:ENSG00000135119 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1383857126 Functional Loss SNV dbSNP153 33..33 33 - - - 27862 RMVar_ID_27862 Human_SNP_ID_517238409 A-to-I Human chr12 + 116851703 116851703 116851703 GTGAAAGTTGCAGTGAGCCGAGATTGCACCACAGCACTCCAACCTGGGTGACAGAGTGAGTGAGA GTGAAAGTTGCAGTGAGCCGAGATTGCACCACCGCACTCCAACCTGGGTGACAGAGTGAGTGAGA A C RNFT2 Ensembl:ENSG00000135119 Protein coding 3'UTR GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1197282976 Functional Loss SNV dbSNP153 33..33 33 - - - 27863 RMVar_ID_27863 Human_SNP_ID_517238410 A-to-I Human chr12 + 116851703 116851703 116851703 GTGAAAGTTGCAGTGAGCCGAGATTGCACCACAGCACTCCAACCTGGGTGACAGAGTGAGTGAGA GTGAAAGTTGCAGTGAGCCGAGATTGCACCACGGCACTCCAACCTGGGTGACAGAGTGAGTGAGA A G RNFT2 Ensembl:ENSG00000135119 Protein coding 3'UTR GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1197282976 Functional Loss SNV dbSNP153 33..33 33 - - - 27864 RMVar_ID_27864 Human_SNP_ID_517238411 A-to-I Human chr12 + 116851703 116851703 116851703 GTGAAAGTTGCAGTGAGCCGAGATTGCACCACAGCACTCCAACCTGGGTGACAGAGTGAGTGAGA GTGAAAGTTGCAGTGAGCCGAGATTGCACCACTGCACTCCAACCTGGGTGACAGAGTGAGTGAGA A T RNFT2 Ensembl:ENSG00000135119 Protein coding 3'UTR GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1197282976 Functional Loss SNV dbSNP153 33..33 33 - - - 27865 RMVar_ID_27865 Human_SNP_ID_517280793 A-to-I Human chr12 + 117029749 117029749 117029749 CTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCGTCCGCTACCACAACTGGCTAATTTTT CTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTGCAGGCGTCCGCTACCACAACTGGCTAATTTTT A G FBXW8 Ensembl:ENSG00000174989 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490832,GSM3490833,GSM3490834 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 31158229,32596459 RNA-Seq:(High) rs1179814708 Functional Loss SNV dbSNP153 33..33 33 - - - 27866 RMVar_ID_27866 Human_SNP_ID_517280801 A-to-I Human chr12 + 117029782 117029782 117029782 CAGGCGTCCGCTACCACAACTGGCTAATTTTTACATTTTTAGTAGAGACGGGGGATATTGCTATG CAGGCGTCCGCTACCACAACTGGCTAATTTTTGCATTTTTAGTAGAGACGGGGGATATTGCTATG A G FBXW8 Ensembl:ENSG00000174989 Protein coding 3'UTR GSE47997;GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,29129909,32596459 RNA-Seq:(High) rs1310649794 Functional Loss SNV dbSNP153 33..33 33 - - - 27867 RMVar_ID_27867 Human_SNP_ID_517280813 A-to-I Human chr12 + 117029847 117029847 117029847 TTGGCCAGGCTGGTCTCAAACTTCTGACCTCAAATGATTGCCTGCCTCAGCCTCCCAAAGTGCTG TTGGCCAGGCTGGTCTCAAACTTCTGACCTCAGATGATTGCCTGCCTCAGCCTCCCAAAGTGCTG A G FBXW8 Ensembl:ENSG00000174989 Protein coding 3'UTR GSE47997;GSE99789 K562 cells&HepG2 cells;esophageal squamous carcinoma cells,EC109 - 23474544,29796672 RNA-Seq:(High) rs1185528398 Functional Loss SNV dbSNP153 33..33 33 - - - 27868 RMVar_ID_27868 Human_SNP_ID_517281267 A-to-I Human chr12 + 117031504 117031504 117031504 GGGAGACCGAGGCAGGCGTATCACCTGAGGTCAGGAGCTCAAGACCAGCCTGGCCAACATGGCAA GGGAGACCGAGGCAGGCGTATCACCTGAGGTCTGGAGCTCAAGACCAGCCTGGCCAACATGGCAA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1163401140 Functional Loss SNV dbSNP153 33..33 33 - - - 27869 RMVar_ID_27869 Human_SNP_ID_517281295 A-to-I Human chr12 + 117031603 117031603 117031603 AGGCCTGGTGGCGTGTGCCTGTAATCACAACTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGCA AGGCCTGGTGGCGTGTGCCTGTAATCACAACTGCTCGGGAGGCTGAGGCAGGAGAATCGCTTGCA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978253147 Functional Loss SNV dbSNP153 33..33 33 - - - 27870 RMVar_ID_27870 Human_SNP_ID_517281308 A-to-I Human chr12 + 117031655 117031655 117031655 AGAATCGCTTGCAGCCAAGAGGCAGAGGTTGCAGTGAGCTGAGATCGCACCACTGCACTCCAGCC AGAATCGCTTGCAGCCAAGAGGCAGAGGTTGCGGTGAGCTGAGATCGCACCACTGCACTCCAGCC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1282125482 Functional Loss SNV dbSNP153 33..33 33 - - - 27871 RMVar_ID_27871 Human_SNP_ID_517320481 A-to-I Human chr12 - 117180763 117180763 117180763 AAAATTAGCTTGGTGTGGTGATGCAGCCTGTAATCCCAGCTATTTGGGAGGCTGAGGCAGGAGAC AAAATTAGCTTGGTGTGGTGATGCAGCCTGTAGTCCCAGCTATTTGGGAGGCTGAGGCAGGAGAC T C FBXO21 Ensembl:ENSG00000135108 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1566007410 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8366786 RMVar_hsa_circ_107764,RMVar_hsa_circ_160517,RMVar_hsa_circ_74996,RMVar_hsa_circ_294161,RMVar_hsa_circ_71151,RMVar_hsa_circ_349902 27872 RMVar_ID_27872 Human_SNP_ID_517321004 A-to-I Human chr12 - 117182408 117182407 117182408 CATGGCTCACTGTAACCTTGAATCCTGTGTTCAGGGGATCCTCTGGCCTCAGCCTCCTGAGTAGC CATGGCTCACTGTAACCTTGAATCCTGTGTTC_GGGGATCCTCTGGCCTCAGCCTCCTGAGTAGC CT C FBXO21 Ensembl:ENSG00000135108 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1330974903 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_107764,RMVar_hsa_circ_160517,RMVar_hsa_circ_74996,RMVar_hsa_circ_294161,RMVar_hsa_circ_71151,RMVar_hsa_circ_349902 27873 RMVar_ID_27873 Human_SNP_ID_517321005 A-to-I Human chr12 - 117182408 117182408 117182408 CATGGCTCACTGTAACCTTGAATCCTGTGTTCAGGGGATCCTCTGGCCTCAGCCTCCTGAGTAGC CATGGCTCACTGTAACCTTGAATCCTGTGTTCTGGGGATCCTCTGGCCTCAGCCTCCTGAGTAGC T A FBXO21 Ensembl:ENSG00000135108 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1445016852 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107764,RMVar_hsa_circ_160517,RMVar_hsa_circ_74996,RMVar_hsa_circ_294161,RMVar_hsa_circ_71151,RMVar_hsa_circ_349902 27874 RMVar_ID_27874 Human_SNP_ID_517321006 A-to-I Human chr12 - 117182408 117182408 117182408 CATGGCTCACTGTAACCTTGAATCCTGTGTTCAGGGGATCCTCTGGCCTCAGCCTCCTGAGTAGC CATGGCTCACTGTAACCTTGAATCCTGTGTTCCGGGGATCCTCTGGCCTCAGCCTCCTGAGTAGC T G FBXO21 Ensembl:ENSG00000135108 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1445016852 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107764,RMVar_hsa_circ_160517,RMVar_hsa_circ_74996,RMVar_hsa_circ_294161,RMVar_hsa_circ_71151,RMVar_hsa_circ_349902 27875 RMVar_ID_27875 Human_SNP_ID_517321209 A-to-I Human chr12 - 117183010 117183010 117183010 TAGCTCACTGCAGACTCAAACCCCTGGGCTCAAGTGACCCTCCTGCCTCAGCCTCCCGAGTAGTT TAGCTCACTGCAGACTCAAACCCCTGGGCTCAGGTGACCCTCCTGCCTCAGCCTCCCGAGTAGTT T C FBXO21 Ensembl:ENSG00000135108 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs902389047 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107764,RMVar_hsa_circ_160517,RMVar_hsa_circ_74996,RMVar_hsa_circ_294161,RMVar_hsa_circ_71151,RMVar_hsa_circ_349902 27876 RMVar_ID_27876 Human_SNP_ID_517328322 A-to-I Human chr12 - 117208783 117208783 117208783 AGGAGGCAGAGGCTGCAGTGAGCCGAGATGGCACCACTGCACTCCAGCTTGTTGACAGAATGAGA AGGAGGCAGAGGCTGCAGTGAGCCGAGATGGCGCCACTGCACTCCAGCTTGTTGACAGAATGAGA T C NOS1 Ensembl:ENSG00000089250 Protein coding 3'UTR GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1204331298 Functional Loss SNV dbSNP153 33..33 33 - - - 27877 RMVar_ID_27877 Human_SNP_ID_517527760 A-to-I Human chr12 + 118024645 118024645 118024645 GTTTTGCCATGTTGGCCAAACCTCCTGACCTCAAGTGATCCTCCCGCCTCAGCCTCCCAAAGTGC GTTTTGCCATGTTGGCCAAACCTCCTGACCTCGAGTGATCCTCCCGCCTCAGCCTCCCAAAGTGC A G RFC5 Ensembl:ENSG00000111445 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs968630692 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_160533,RMVar_hsa_circ_120416,RMVar_hsa_circ_320245,RMVar_hsa_circ_160534,RMVar_hsa_circ_125799,RMVar_hsa_circ_280046,RMVar_hsa_circ_344602,RMVar_hsa_circ_297662,RMVar_hsa_circ_160535,RMVar_hsa_circ_160536,RMVar_hsa_circ_104474,RMVar_hsa_circ_114278,RMVar_hsa_circ_160540,RMVar_hsa_circ_160541 27878 RMVar_ID_27878 Human_SNP_ID_517531204 A-to-I Human chr12 + 118038729 118038729 118038729 TGGAGTCTTGCTCTTGCTCTGTCTCCCAGACTAGAATACAGTGGCGCGATCTCAGCTCACTGCAA TGGAGTCTTGCTCTTGCTCTGTCTCCCAGACTGGAATACAGTGGCGCGATCTCAGCTCACTGCAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs927786976 Functional Loss SNV dbSNP153 33..33 33 - - - 27879 RMVar_ID_27879 Human_SNP_ID_517531230 A-to-I Human chr12 + 118038864 118038859 118038864 CACTGCGCCCAGCTCATTTTTGTACTTTTAGTAGAGACAGGGTTTCACCATATTGGCCAGGCTGG CACTGCGCCCAGCTCATTTTTGTACTTT_____GAGACAGGGTTTCACCATATTGGCCAGGCTGG TTAGTA T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1313703420 Functional Loss DEL dbSNP153 29..33 33 - - - 27880 RMVar_ID_27880 Human_SNP_ID_517531525 A-to-I Human chr12 + 118040112 118040112 118040112 GGAGGATCACTGGAGCCCAGGAGGCAGAGGCTACAATAAGCCGAGATCGCAGCATTGCACTCCAG GGAGGATCACTGGAGCCCAGGAGGCAGAGGCTGCAATAAGCCGAGATCGCAGCATTGCACTCCAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs949712965 Functional Loss SNV dbSNP153 33..33 33 - - - 27881 RMVar_ID_27881 Human_SNP_ID_517531710 A-to-I Human chr12 - 118040830 118040830 118040830 TTGGCCAGGCTGGTCTCAAACTCCTGACCTCAAGTGATCTGCCTACCTGGGCTTCCTAAAGTGCT TTGGCCAGGCTGGTCTCAAACTCCTGACCTCAGGTGATCTGCCTACCTGGGCTTCCTAAAGTGCT T C WSB2 Ensembl:ENSG00000176871 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1287130204 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43489,RMVar_hsa_circ_14306,RMVar_hsa_circ_314695,RMVar_hsa_circ_160546,RMVar_hsa_circ_305785,RMVar_hsa_circ_160549,RMVar_hsa_circ_160551,RMVar_hsa_circ_106798,RMVar_hsa_circ_377956,RMVar_hsa_circ_160550 27882 RMVar_ID_27882 Human_SNP_ID_517531731 A-to-I Human chr12 - 118040941 118040941 118040941 AGGTTCAAGTCATTCTTGTGTCTCAGCCTCCCAAGTAGCTGGGACTACAGGCGTAAGCCACCATA AGGTTCAAGTCATTCTTGTGTCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGTAAGCCACCATA T C WSB2 Ensembl:ENSG00000176871 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1476344670 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43489,RMVar_hsa_circ_14306,RMVar_hsa_circ_314695,RMVar_hsa_circ_160546,RMVar_hsa_circ_305785,RMVar_hsa_circ_160549,RMVar_hsa_circ_160551,RMVar_hsa_circ_106798,RMVar_hsa_circ_377956,RMVar_hsa_circ_160550 27883 RMVar_ID_27883 Human_SNP_ID_517535459 A-to-I Human chr12 - 118056644 118056644 118056644 TGCCTGCCTCGGCCTCCCAAAGTGTTGGGATTACAAGCATGAGCTACCATGCCTGGCCAGCTTTA TGCCTGCCTCGGCCTCCCAAAGTGTTGGGATTGCAAGCATGAGCTACCATGCCTGGCCAGCTTTA T C WSB2 Ensembl:ENSG00000176871 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202575320 Functional Loss SNV dbSNP153 33..33 33 - - - 27884 RMVar_ID_27884 Human_SNP_ID_517536335 A-to-I Human chr12 - 118060245 118060245 118060245 GGATATACCTCAAGCCAGCCCAGATGAACATAAAATCTCAGTGGGAAAGGTGTGTCTCTTATGCA GGATATACCTCAAGCCAGCCCAGATGAACATATAATCTCAGTGGGAAAGGTGTGTCTCTTATGCA T A WSB2 Ensembl:ENSG00000176871 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1479106051 Functional Loss SNV dbSNP153 33..33 33 - - - 27885 RMVar_ID_27885 Human_SNP_ID_517538913 A-to-I Human chr12 - 118069112 118069112 118069112 GCACTCTAGCCTGGGCAACAGCGCAAGACTCTATCCCGAAAAAGAAAAAAAAAAGAAATGTATAG GCACTCTAGCCTGGGCAACAGCGCAAGACTCTGTCCCGAAAAAGAAAAAAAAAAGAAATGTATAG T C VSIG10 Ensembl:ENSG00000176834 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1205192031 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 27886 RMVar_ID_27886 Human_SNP_ID_517538938 A-to-I Human chr12 - 118069218 118069218 118069218 AGATGTGGTGGCGCATGCCTGTAGTCCCAGCTACTTGGGTGGCTGAGGCAGGAGAATTGCTTGCA AGATGTGGTGGCGCATGCCTGTAGTCCCAGCTGCTTGGGTGGCTGAGGCAGGAGAATTGCTTGCA T C VSIG10 Ensembl:ENSG00000176834 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1390176120 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 27887 RMVar_ID_27887 Human_SNP_ID_517538939 A-to-I Human chr12 - 118069218 118069218 118069218 AGATGTGGTGGCGCATGCCTGTAGTCCCAGCTACTTGGGTGGCTGAGGCAGGAGAATTGCTTGCA AGATGTGGTGGCGCATGCCTGTAGTCCCAGCTCCTTGGGTGGCTGAGGCAGGAGAATTGCTTGCA T G VSIG10 Ensembl:ENSG00000176834 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1390176120 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 27888 RMVar_ID_27888 Human_SNP_ID_517539260 A-to-I Human chr12 - 118070331 118070331 118070331 GTTGCCCAGGCTAGTCTCAAACTCCTGGCCTCAAGTGGTCTGCCCGCCTCGGCCTCCCAAAGTGC GTTGCCCAGGCTAGTCTCAAACTCCTGGCCTCGAGTGGTCTGCCCGCCTCGGCCTCCCAAAGTGC T C VSIG10 Ensembl:ENSG00000176834 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1250032386 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 27889 RMVar_ID_27889 Human_SNP_ID_517551272 A-to-I Human chr12 - 118114434 118114434 118114434 TGAACCTGGGAAGCGGAGATTGCAGTAAGCCAAGATTGAGCCACTGCACTCCAGCCTGGGCTACG TGAACCTGGGAAGCGGAGATTGCAGTAAGCCAGGATTGAGCCACTGCACTCCAGCCTGGGCTACG T C VSIG10 Ensembl:ENSG00000176834 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1158057315 Functional Loss SNV dbSNP153 33..33 33 - - - 27890 RMVar_ID_27890 Human_SNP_ID_517551273 A-to-I Human chr12 - 118114435 118114435 118114435 TTGAACCTGGGAAGCGGAGATTGCAGTAAGCCAAGATTGAGCCACTGCACTCCAGCCTGGGCTAC TTGAACCTGGGAAGCGGAGATTGCAGTAAGCCGAGATTGAGCCACTGCACTCCAGCCTGGGCTAC T C VSIG10 Ensembl:ENSG00000176834 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1440337071 Functional Loss SNV dbSNP153 33..33 33 - - - 27891 RMVar_ID_27891 Human_SNP_ID_517551518 A-to-I Human chr12 - 118115633 118115633 118115633 GTGCCATCATGCCCGGCTAATTTTATATTTTTAGTAGAGACAGGGTTTCTCCATGTTGGTCAGGC GTGCCATCATGCCCGGCTAATTTTATATTTTTCGTAGAGACAGGGTTTCTCCATGTTGGTCAGGC T G VSIG10 Ensembl:ENSG00000176834 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1341539666 Functional Loss SNV dbSNP153 33..33 33 - - - 27892 RMVar_ID_27892 Human_SNP_ID_517551740 A-to-I Human chr12 - 118116603 118116603 118116603 TGGAGTGCCACAGCGCGATCTCTGCTCACTACAACCTCCATCTCCCAGGCTCAAGCACTCCTCCC TGGAGTGCCACAGCGCGATCTCTGCTCACTACTACCTCCATCTCCCAGGCTCAAGCACTCCTCCC T A VSIG10 Ensembl:ENSG00000176834 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs922030164 Functional Loss SNV dbSNP153 33..33 33 - - - 27893 RMVar_ID_27893 Human_SNP_ID_517551741 A-to-I Human chr12 - 118116605 118116605 118116605 GCTGGAGTGCCACAGCGCGATCTCTGCTCACTACAACCTCCATCTCCCAGGCTCAAGCACTCCTC GCTGGAGTGCCACAGCGCGATCTCTGCTCACTGCAACCTCCATCTCCCAGGCTCAAGCACTCCTC T C VSIG10 Ensembl:ENSG00000176834 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1566188449 Functional Loss SNV dbSNP153 33..33 33 - - - 27894 RMVar_ID_27894 Human_SNP_ID_517551758 A-to-I Human chr12 - 118116663 118116663 118116663 CCATTCTATCTTTTTTATTTTTTATTTTTTTGAGACAGGGTCTCGCTCTGTCACTCAGGCTGGAG CCATTCTATCTTTTTTATTTTTTATTTTTTTGTGACAGGGTCTCGCTCTGTCACTCAGGCTGGAG T A VSIG10 Ensembl:ENSG00000176834 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1281687367 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6140433,Human_RBP_ID_11836455,Human_RBP_ID_26412396 27895 RMVar_ID_27895 Human_SNP_ID_517551795 A-to-I Human chr12 - 118116815 118116815 118116815 ACTCTGGAGGCTGAGGCACGAAAATTGCTTGAACCCAGGAGGTGGAGGTTGCATTGAACCAAGAT ACTCTGGAGGCTGAGGCACGAAAATTGCTTGATCCCAGGAGGTGGAGGTTGCATTGAACCAAGAT T A VSIG10 Ensembl:ENSG00000176834 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs765315523 Functional Loss SNV dbSNP153 33..33 33 - - - 27896 RMVar_ID_27896 Human_SNP_ID_517551932 A-to-I Human chr12 - 118117462 118117462 118117462 AGGCCTCACCATATTGGCCAGGCTGTTCTCGAACTCCGGACCTTAGGTGATCTGCCTGCCTCAGC AGGCCTCACCATATTGGCCAGGCTGTTCTCGATCTCCGGACCTTAGGTGATCTGCCTGCCTCAGC T A VSIG10 Ensembl:ENSG00000176834 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913524541 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11836458 27897 RMVar_ID_27897 Human_SNP_ID_517551933 A-to-I Human chr12 - 118117462 118117462 118117462 AGGCCTCACCATATTGGCCAGGCTGTTCTCGAACTCCGGACCTTAGGTGATCTGCCTGCCTCAGC AGGCCTCACCATATTGGCCAGGCTGTTCTCGAGCTCCGGACCTTAGGTGATCTGCCTGCCTCAGC T C VSIG10 Ensembl:ENSG00000176834 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913524541 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11836458 27898 RMVar_ID_27898 Human_SNP_ID_517551937 A-to-I Human chr12 - 118117484 118117484 118117484 TTTTGTATTTTTAGTAGAGACGAGGCCTCACCATATTGGCCAGGCTGTTCTCGAACTCCGGACCT TTTTGTATTTTTAGTAGAGACGAGGCCTCACCGTATTGGCCAGGCTGTTCTCGAACTCCGGACCT T C VSIG10 Ensembl:ENSG00000176834 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1486878161 Functional Loss SNV dbSNP153 33..33 33 - - - 27899 RMVar_ID_27899 Human_SNP_ID_517551938 A-to-I Human chr12 - 118117487 118117487 118117487 AATTTTTGTATTTTTAGTAGAGACGAGGCCTCACCATATTGGCCAGGCTGTTCTCGAACTCCGGA AATTTTTGTATTTTTAGTAGAGACGAGGCCTCGCCATATTGGCCAGGCTGTTCTCGAACTCCGGA T C VSIG10 Ensembl:ENSG00000176834 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs868076777 Functional Loss SNV dbSNP153 33..33 33 - - - 27900 RMVar_ID_27900 Human_SNP_ID_517551967 A-to-I Human chr12 - 118117583 118117583 118117583 GGCTCACTGCAACCTCTGCCTCCCGGGTTAAAACGATTCTCCTGCCTCAGCGTCCCAAGTAGCTG GGCTCACTGCAACCTCTGCCTCCCGGGTTAAAGCGATTCTCCTGCCTCAGCGTCCCAAGTAGCTG T C VSIG10 Ensembl:ENSG00000176834 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1172945241 Functional Loss SNV dbSNP153 33..33 33 - - - 27901 RMVar_ID_27901 Human_SNP_ID_517557367 A-to-I Human chr12 + 118137494 118137494 118137494 GATCGATCGATTGAGCGCTGGAGGTTGAGGCTACAGTGAGCCTTGATAGCGTCACTACACTCCGG GATCGATCGATTGAGCGCTGGAGGTTGAGGCTGCAGTGAGCCTTGATAGCGTCACTACACTCCGG A G PEBP1 Ensembl:ENSG00000089220 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1318326964 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17561295 RMVar_hsa_circ_121207,RMVar_hsa_circ_160564 27902 RMVar_ID_27902 Human_SNP_ID_517557375 A-to-I Human chr12 + 118137518 118137518 118137518 TTGAGGCTACAGTGAGCCTTGATAGCGTCACTACACTCCGGCCTGAGTGACAGAAGGAGACCTGG TTGAGGCTACAGTGAGCCTTGATAGCGTCACTGCACTCCGGCCTGAGTGACAGAAGGAGACCTGG A G PEBP1 Ensembl:ENSG00000089220 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1190164188 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17561295 RMVar_hsa_circ_121207,RMVar_hsa_circ_160564 27903 RMVar_ID_27903 Human_SNP_ID_517558198 A-to-I Human chr12 + 118140720 118140718 118140721 GCCACCATGCCTGGCTAATTTTATGCATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGA GCCACCATGCCTGGCTAATTTTATGCATTTT___TAGAGACGGGGTTTCACCGTGTTAGCCAGGA TTAG T PEBP1 Ensembl:ENSG00000089220 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1043781094 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_110913,RMVar_hsa_circ_160565 27904 RMVar_ID_27904 Human_SNP_ID_517558364 A-to-I Human chr12 + 118141278 118141278 118141278 AGCTGGGATGACAGGCGCCCACCACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGTCAAGGT AGCTGGGATGACAGGCGCCCACCACCACGCCCCGCTAATTTTTGTATTTTTAGTAGAGTCAAGGT A C PEBP1 Ensembl:ENSG00000089220 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1007527131 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110913,RMVar_hsa_circ_160565 27905 RMVar_ID_27905 Human_SNP_ID_517558365 A-to-I Human chr12 + 118141278 118141278 118141278 AGCTGGGATGACAGGCGCCCACCACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGTCAAGGT AGCTGGGATGACAGGCGCCCACCACCACGCCCGGCTAATTTTTGTATTTTTAGTAGAGTCAAGGT A G PEBP1 Ensembl:ENSG00000089220 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1007527131 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110913,RMVar_hsa_circ_160565 27906 RMVar_ID_27906 Human_SNP_ID_517558560 A-to-I Human chr12 + 118141993 118141991 118141994 ATTATCCAGTCTTTTTGTTTAAACTTCTGTGTATTATTCTAGGACTATTTAGCTTTGAAAAGAAA ATTATCCAGTCTTTTTGTTTAAACTTCTGTG___TATTCTAGGACTATTTAGCTTTGAAAAGAAA GTAT G PEBP1 Ensembl:ENSG00000089220 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs910933840 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_110913,RMVar_hsa_circ_160565 27907 RMVar_ID_27907 Human_SNP_ID_517558565 A-to-I Human chr12 + 118142020 118142020 118142020 TGTGTATTATTCTAGGACTATTTAGCTTTGAAAAGAAATTTGGGCACATGCTACACCAGGATGAA TGTGTATTATTCTAGGACTATTTAGCTTTGAAGAGAAATTTGGGCACATGCTACACCAGGATGAA A G PEBP1 Ensembl:ENSG00000089220 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1319301968 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110913,RMVar_hsa_circ_160565 27908 RMVar_ID_27908 Human_SNP_ID_517558957 A-to-I Human chr12 + 118143344 118143344 118143344 GGAATTGTACAGTATTTGTCTTGCGACTGGCTAATTTCACTAATGTAATGTTCTCAAGGTTCTCT GGAATTGTACAGTATTTGTCTTGCGACTGGCTCATTTCACTAATGTAATGTTCTCAAGGTTCTCT A C PEBP1 Ensembl:ENSG00000089220 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1432709435 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110913,RMVar_hsa_circ_160565 27909 RMVar_ID_27909 Human_SNP_ID_517561995 A-to-I Human chr12 - 118154577 118154575 118154578 AAATTAGCTGGGCCTGGTGGCACTTACCTGTAATCTCAGCTACTCGGGAGGATGAGGCAGGAGAA AAATTAGCTGGGCCTGGTGGCACTTACCTGT___CTCAGCTACTCGGGAGGATGAGGCAGGAGAA GATT G TAOK3 Ensembl:ENSG00000135090 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs533731258 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_24615,RMVar_hsa_circ_117399,RMVar_hsa_circ_160572,RMVar_hsa_circ_160573 27910 RMVar_ID_27910 Human_SNP_ID_517577199 A-to-I Human chr12 - 118219283 118219283 118219283 ACGCCACTGCACTCCAGCCTGGGCAACAGAGCAAGACCCCGACACACACACACATACACAAAAAG ACGCCACTGCACTCCAGCCTGGGCAACAGAGCGAGACCCCGACACACACACACATACACAAAAAG T C TAOK3 Ensembl:ENSG00000135090 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1053373745 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8836,RMVar_hsa_circ_78651,RMVar_hsa_circ_73600,RMVar_hsa_circ_123604,RMVar_hsa_circ_160579,RMVar_hsa_circ_27687,RMVar_hsa_circ_72578,RMVar_hsa_circ_160585,RMVar_hsa_circ_93279,RMVar_hsa_circ_160588,RMVar_hsa_circ_160589,RMVar_hsa_circ_25405 27911 RMVar_ID_27911 Human_SNP_ID_517584541 A-to-I Human chr12 - 118249834 118249834 118249834 CACTTTTAAAATTTTTATTTATTCATTTATTTAGAGACAGGGTCTCTCACTCTGTCACCCAAGCT CACTTTTAAAATTTTTATTTATTCATTTATTTTGAGACAGGGTCTCTCACTCTGTCACCCAAGCT T A TAOK3 Ensembl:ENSG00000135090 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs772702791 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6140566 RMVar_hsa_circ_78651,RMVar_hsa_circ_73600,RMVar_hsa_circ_160579,RMVar_hsa_circ_72578,RMVar_hsa_circ_160589,RMVar_hsa_circ_61777,RMVar_hsa_circ_321109,RMVar_hsa_circ_358043,RMVar_hsa_circ_337137,RMVar_hsa_circ_160596,RMVar_hsa_circ_160599,RMVar_hsa_circ_356584,RMVar_hsa_circ_358811,RMVar_hsa_circ_290373 27912 RMVar_ID_27912 Human_SNP_ID_517594651 A-to-I Human chr12 - 118293971 118293971 118293972 CCCTCTTGTTGCCTAGGCTGGAGTGCAATGGCATGATCTCGGCTCACCGCAACCTCTGCCTCCCG CCCTCTTGTTGCCTAGGCTGGAGTGCAATGGTGTGATCTCGGCTCACCGCAACCTCTGCCTCCCG TG CA TAOK3 Ensembl:ENSG00000135090 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs71450270 Functional Loss MNV dbSNP153 32..33 33 - - - RMVar_hsa_circ_350697 27913 RMVar_ID_27913 Human_SNP_ID_517594652 A-to-I Human chr12 - 118293971 118293971 118293971 CCCTCTTGTTGCCTAGGCTGGAGTGCAATGGCATGATCTCGGCTCACCGCAACCTCTGCCTCCCG CCCTCTTGTTGCCTAGGCTGGAGTGCAATGGCGTGATCTCGGCTCACCGCAACCTCTGCCTCCCG T C TAOK3 Ensembl:ENSG00000135090 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1382379730 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_350697 27914 RMVar_ID_27914 Human_SNP_ID_517598129 A-to-I Human chr12 - 118310129 118310129 118310129 CAGGTGCACGCCACTATGCCCAGCTAATTTTTATATTTTATTGTAGAAATTGGGTTTTGCCATGT CAGGTGCACGCCACTATGCCCAGCTAATTTTTGTATTTTATTGTAGAAATTGGGTTTTGCCATGT T C TAOK3 Ensembl:ENSG00000135090 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432138258 Functional Loss SNV dbSNP153 33..33 33 - - - 27915 RMVar_ID_27915 Human_SNP_ID_517599587 A-to-I Human chr12 - 118317051 118317051 118317051 GCCATGTTGGCCAGGCTGGTCTCGAACTCCTGAGCTCAAGCAATCCACCCACCTTGGCCTCCCAA GCCATGTTGGCCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAATCCACCCACCTTGGCCTCCCAA T C TAOK3 Ensembl:ENSG00000135090 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025915287 Functional Loss SNV dbSNP153 33..33 33 - - - 27916 RMVar_ID_27916 Human_SNP_ID_517611052 A-to-I Human chr12 - 118367027 118367027 118367027 TTTCGAGACAGCCTTACTCTGTCGCCCAGGCTAGACTTCAGTGGTGCCATCTCGGCTTACTGCAA TTTCGAGACAGCCTTACTCTGTCGCCCAGGCTGGACTTCAGTGGTGCCATCTCGGCTTACTGCAA T C TAOK3 Ensembl:ENSG00000135090 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1381035197 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_755659,Human_RBP_ID_11836933 27917 RMVar_ID_27917 Human_SNP_ID_517611474 A-to-I Human chr12 - 118368637 118368637 118368637 CACACCCGGCTAATGTTTGTATTTTTATTAGAAGCGGTTTTTCACCACGGTGGCCAGGCTGATCT CACACCCGGCTAATGTTTGTATTTTTATTAGAGGCGGTTTTTCACCACGGTGGCCAGGCTGATCT T C TAOK3 Ensembl:ENSG00000135090 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1566184329 Functional Loss SNV dbSNP153 33..33 33 - - - 27918 RMVar_ID_27918 Human_SNP_ID_517617019 A-to-I Human chr12 + 118389581 118389581 118389581 TCACCCAGGCTGTAGTACAGTGGCACAATCTCAGCTTACTGCAACCTCTGCCGCTCAGGTTCAAG TCACCCAGGCTGTAGTACAGTGGCACAATCTCGGCTTACTGCAACCTCTGCCGCTCAGGTTCAAG A G SUDS3 Ensembl:ENSG00000111707 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1183981175 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_355701,RMVar_hsa_circ_362083,RMVar_hsa_circ_298484,RMVar_hsa_circ_344831,RMVar_hsa_circ_355725 27919 RMVar_ID_27919 Human_SNP_ID_517927828 A-to-I Human chr12 - 119696951 119696951 119696951 GCAGTTAAATAAATTAAAGTACAGCCCTGGGAAGGAATGTTGTGCAGGCATCTGGGGAAAAGAAT GCAGTTAAATAAATTAAAGTACAGCCCTGGGACGGAATGTTGTGCAGGCATCTGGGGAAAAGAAT T G CIT Ensembl:ENSG00000122966 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs570582257 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113903,RMVar_hsa_circ_160609 27920 RMVar_ID_27920 Human_SNP_ID_517927833 A-to-I Human chr12 - 119696963 119696963 119696963 ATTGATAAAGAAGCAGTTAAATAAATTAAAGTACAGCCCTGGGAAGGAATGTTGTGCAGGCATCT ATTGATAAAGAAGCAGTTAAATAAATTAAAGTGCAGCCCTGGGAAGGAATGTTGTGCAGGCATCT T C CIT Ensembl:ENSG00000122966 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934512903 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24937293 RMVar_hsa_circ_113903,RMVar_hsa_circ_160609 27921 RMVar_ID_27921 Human_SNP_ID_517954941 A-to-I Human chr12 - 119811068 119811068 119811068 CACCTGCTTTGGCCTCCTAAAATGCTGGGATTACAAGTGTTAGCCACCAGGCCCGGTCTTGAACT CACCTGCTTTGGCCTCCTAAAATGCTGGGATTGCAAGTGTTAGCCACCAGGCCCGGTCTTGAACT T C CIT Ensembl:ENSG00000122966 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006009367 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26447,RMVar_hsa_circ_16497,RMVar_hsa_circ_18128,RMVar_hsa_circ_42262,RMVar_hsa_circ_160631,RMVar_hsa_circ_123049,RMVar_hsa_circ_327345,RMVar_hsa_circ_293385,RMVar_hsa_circ_160632,RMVar_hsa_circ_160633 27922 RMVar_ID_27922 Human_SNP_ID_517954943 A-to-I Human chr12 - 119811079 119811079 119811079 CTGAAGTGATCCACCTGCTTTGGCCTCCTAAAATGCTGGGATTACAAGTGTTAGCCACCAGGCCC CTGAAGTGATCCACCTGCTTTGGCCTCCTAAAGTGCTGGGATTACAAGTGTTAGCCACCAGGCCC T C CIT Ensembl:ENSG00000122966 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1038449595 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26447,RMVar_hsa_circ_16497,RMVar_hsa_circ_18128,RMVar_hsa_circ_42262,RMVar_hsa_circ_160631,RMVar_hsa_circ_123049,RMVar_hsa_circ_327345,RMVar_hsa_circ_293385,RMVar_hsa_circ_160632,RMVar_hsa_circ_160633 27923 RMVar_ID_27923 Human_SNP_ID_518000820 A-to-I Human chr12 + 119993224 119993224 119993224 TGACCTCGTGATCCGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGCGC TGACCTCGTGATCCGCCTGCCTCGGCCTCCCAGAGTGCTGGGATTACAGGCATGAGCCACTGCGC A G BICDL1 Ensembl:ENSG00000135127 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs191231481 Functional Loss SNV dbSNP153 33..33 33 - - - 27924 RMVar_ID_27924 Human_SNP_ID_713121272 A-to-I Human chrX + 30699477 30699477 30699477 AACCCCGCCTCCTGAGTTCAAGTGATTCTTCCACCTCAGCCTCCTGAGTAGCTGGGATTACAGGT AACCCCGCCTCCTGAGTTCAAGTGATTCTTCCCCCTCAGCCTCCTGAGTAGCTGGGATTACAGGT A C AC112496.1,GK Ensembl:ENSG00000241886,Ensembl:ENSG00000198814 lincRNA,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1179834264 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_152,RMVar_hsa_circ_65363 27925 RMVar_ID_27925 Human_SNP_ID_713146747 A-to-I Human chrX - 30834836 30834836 30834836 CTTGAGGCCAGGAGTTTGAGACCAGCCTGGGCAACATAGCGAGAGACCCTGTCTCTACAAAAAAT CTTGAGGCCAGGAGTTTGAGACCAGCCTGGGCGACATAGCGAGAGACCCTGTCTCTACAAAAAAT T C TAB3 Ensembl:ENSG00000157625 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs910340676 Functional Loss SNV dbSNP153 33..33 33 - - - 27926 RMVar_ID_27926 Human_SNP_ID_713146751 A-to-I Human chrX - 30834904 30834904 30834904 AAATCCACCAGACACAGTGGCTCCTGCCTGTAATACCAACACTTTGGGAGGCTGAGGTGGGAGGA AAATCCACCAGACACAGTGGCTCCTGCCTGTAGTACCAACACTTTGGGAGGCTGAGGTGGGAGGA T C TAB3 Ensembl:ENSG00000157625 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1269613513 Functional Loss SNV dbSNP153 33..33 33 - - - 27927 RMVar_ID_27927 Human_SNP_ID_713147030 A-to-I Human chrX - 30836586 30836586 30836586 CTGCTGCCTTGGCCTCCCAAAGTGCTGCGATTACAGGCATAAGTCACTGTTCCTGGTCTGAAAGA CTGCTGCCTTGGCCTCCCAAAGTGCTGCGATTGCAGGCATAAGTCACTGTTCCTGGTCTGAAAGA T C TAB3 Ensembl:ENSG00000157625 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1375366809 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26273631 27928 RMVar_ID_27928 Human_SNP_ID_713147043 A-to-I Human chrX - 30836660 30836660 30836660 TTGTGTATTTTTTGTGGAGACAGGGTTTCGCCATGTTGCCCGGGCTGGTCTCAAACTCCTGGGCT TTGTGTATTTTTTGTGGAGACAGGGTTTCGCCGTGTTGCCCGGGCTGGTCTCAAACTCCTGGGCT T C TAB3 Ensembl:ENSG00000157625 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256694900 Functional Loss SNV dbSNP153 33..33 33 - - - 27929 RMVar_ID_27929 Human_SNP_ID_713147078 A-to-I Human chrX - 30836791 30836791 30836791 TCGCCCAGGCTGGAGTGCAGTGGCATGATCATAGCTCATTGCAGCCTCGACCTCCCAGGCTCAAG TCGCCCAGGCTGGAGTGCAGTGGCATGATCATGGCTCATTGCAGCCTCGACCTCCCAGGCTCAAG T C TAB3 Ensembl:ENSG00000157625 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1380267064 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2193947 27930 RMVar_ID_27930 Human_SNP_ID_713220634 A-to-I Human chrX - 31250999 31250999 31250999 TAGCTCACTGCAAACTCTGCCTCCCGGGTTCAAGCGATTTTCCTGCCTCAGCCTCCCGAGTAGCT TAGCTCACTGCAAACTCTGCCTCCCGGGTTCAGGCGATTTTCCTGCCTCAGCCTCCCGAGTAGCT T C DMD Ensembl:ENSG00000198947 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1351692207 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9219,RMVar_hsa_circ_62994,RMVar_hsa_circ_39106,RMVar_hsa_circ_369243,RMVar_hsa_circ_22794,RMVar_hsa_circ_36561,RMVar_hsa_circ_62868 27931 RMVar_ID_27931 Human_SNP_ID_713332515 A-to-I Human chrX - 31863176 31863176 31863176 ACCACGCCCGGCTAATTTTGTGTATTTTTAGTAGAGGCGGGGTTTCACCATGTTAGCCAGGATGG ACCACGCCCGGCTAATTTTGTGTATTTTTAGTGGAGGCGGGGTTTCACCATGTTAGCCAGGATGG T C DMD Ensembl:ENSG00000198947 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1399250480 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_666,RMVar_hsa_circ_22794,RMVar_hsa_circ_36561,RMVar_hsa_circ_62868,RMVar_hsa_circ_358301,RMVar_hsa_circ_353188,RMVar_hsa_circ_348511,RMVar_hsa_circ_27377,RMVar_hsa_circ_21984,RMVar_hsa_circ_357119,RMVar_hsa_circ_358734,RMVar_hsa_circ_368185,RMVar_hsa_circ_366280,RMVar_hsa_circ_42455,RMVar_hsa_circ_367044,RMVar_hsa_circ_18485,RMVar_hsa_circ_352197,RMVar_hsa_circ_351386,RMVar_hsa_circ_281744,RMVar_hsa_circ_52844,RMVar_hsa_circ_361811,RMVar_hsa_circ_323455,RMVar_hsa_circ_329501,RMVar_hsa_circ_296203,RMVar_hsa_circ_351027,RMVar_hsa_circ_351483,RMVar_hsa_circ_358956,RMVar_hsa_circ_302449,RMVar_hsa_circ_62057,RMVar_hsa_circ_290013,RMVar_hsa_circ_352437,RMVar_hsa_circ_73562,RMVar_hsa_circ_32201,RMVar_hsa_circ_351117,RMVar_hsa_circ_261920,RMVar_hsa_circ_343741 27932 RMVar_ID_27932 Human_SNP_ID_713332531 A-to-I Human chrX - 31863221 31863221 31863221 CTCCTGCGTCATCCTCCCGAGCAGCTGGGACTACAGGCGCCCGCCACCACGCCCGGCTAATTTTG CTCCTGCGTCATCCTCCCGAGCAGCTGGGACTGCAGGCGCCCGCCACCACGCCCGGCTAATTTTG T C DMD Ensembl:ENSG00000198947 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1323033759 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_666,RMVar_hsa_circ_22794,RMVar_hsa_circ_36561,RMVar_hsa_circ_62868,RMVar_hsa_circ_358301,RMVar_hsa_circ_353188,RMVar_hsa_circ_348511,RMVar_hsa_circ_27377,RMVar_hsa_circ_21984,RMVar_hsa_circ_357119,RMVar_hsa_circ_358734,RMVar_hsa_circ_368185,RMVar_hsa_circ_366280,RMVar_hsa_circ_42455,RMVar_hsa_circ_367044,RMVar_hsa_circ_18485,RMVar_hsa_circ_352197,RMVar_hsa_circ_351386,RMVar_hsa_circ_281744,RMVar_hsa_circ_52844,RMVar_hsa_circ_361811,RMVar_hsa_circ_323455,RMVar_hsa_circ_329501,RMVar_hsa_circ_296203,RMVar_hsa_circ_351027,RMVar_hsa_circ_351483,RMVar_hsa_circ_358956,RMVar_hsa_circ_302449,RMVar_hsa_circ_62057,RMVar_hsa_circ_290013,RMVar_hsa_circ_352437,RMVar_hsa_circ_73562,RMVar_hsa_circ_32201,RMVar_hsa_circ_351117,RMVar_hsa_circ_261920,RMVar_hsa_circ_343741 27933 RMVar_ID_27933 Human_SNP_ID_714522591 A-to-I Human chrX + 38479774 38479774 38479774 ACACACTGATCCTGCCAGAAAATTTCAAAGACAATAGATCAAAAAAGAAAGGTTTGGTAAAAAAA ACACACTGATCCTGCCAGAAAATTTCAAAGACGATAGATCAAAAAAGAAAGGTTTGGTAAAAAAA A G AF241726.1,AF241726.2 Ensembl:ENSG00000232370,Ensembl:ENSG00000250349 Pseudogene,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1339754438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18543518 27934 RMVar_ID_27934 Human_SNP_ID_714746450 A-to-I Human chrX - 39788155 39788155 39788155 TCAGCCGCATCTTCTTTTGCATCGTCAGCCAAACCACATCCCTGAGACACCATGGGGAAGGTGAA TCAGCCGCATCTTCTTTTGCATCGTCAGCCAAGCCACATCCCTGAGACACCATGGGGAAGGTGAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs760512065 Functional Loss SNV dbSNP153 33..33 33 - - - 27935 RMVar_ID_27935 Human_SNP_ID_714746451 A-to-I Human chrX - 39788157 39788157 39788157 AGTCAGCCGCATCTTCTTTTGCATCGTCAGCCAAACCACATCCCTGAGACACCATGGGGAAGGTG AGTCAGCCGCATCTTCTTTTGCATCGTCAGCCGAACCACATCCCTGAGACACCATGGGGAAGGTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs763992138 Functional Loss SNV dbSNP153 33..33 33 - - - 27936 RMVar_ID_27936 Human_SNP_ID_714746455 A-to-I Human chrX - 39788167 39788167 39788167 CCTGTTCTACAGTCAGCCGCATCTTCTTTTGCATCGTCAGCCAAACCACATCCCTGAGACACCAT CCTGTTCTACAGTCAGCCGCATCTTCTTTTGCGTCGTCAGCCAAACCACATCCCTGAGACACCAT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs766590874 Functional Loss SNV dbSNP153 33..33 33 - - - 27937 RMVar_ID_27937 Human_SNP_ID_714895365 A-to-I Human chrX + 40602995 40602995 40602995 TTACTCTGTCACCCAGACTGGAGTGCAGTGGCACAATCTCAACTCACTGCAGCCTCCACCTCCCA TTACTCTGTCACCCAGACTGGAGTGCAGTGGCTCAATCTCAACTCACTGCAGCCTCCACCTCCCA A T ATP6AP2 Ensembl:ENSG00000182220 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1266036580 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76843,RMVar_hsa_circ_110825,RMVar_hsa_circ_261995,RMVar_hsa_circ_114411,RMVar_hsa_circ_261996,RMVar_hsa_circ_261997,RMVar_hsa_circ_261998,RMVar_hsa_circ_94884 27938 RMVar_ID_27938 Human_SNP_ID_714902988 A-to-I Human chrX - 40640818 40640818 40640818 CTCCTGCCTTAGCTTCCCAAGTAGCTGGGATTACAGGCGCGTGCCACCACGCCTGGCTGGTTTTT CTCCTGCCTTAGCTTCCCAAGTAGCTGGGATTCCAGGCGCGTGCCACCACGCCTGGCTGGTTTTT T G CXorf38 Ensembl:ENSG00000185753 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs931784215 Functional Loss SNV dbSNP153 33..33 33 - - - 27939 RMVar_ID_27939 Human_SNP_ID_714914067 A-to-I Human chrX - 40709372 40709372 40709372 ATCAGAAGCTCCAAGAACTGAAGGCCATTCTTAGAGGCTTCAATGCCAATGAAAACTGTAGGTTC ATCAGAAGCTCCAAGAACTGAAGGCCATTCTTGGAGGCTTCAATGCCAATGAAAACTGTAGGTTC T C MED14 Ensembl:ENSG00000180182 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1329703963 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3976375 Human_Splice_Rec_2197167,Human_Splice_Rec_2197168 RMVar_hsa_circ_109033,RMVar_hsa_circ_262007,RMVar_hsa_circ_89277,RMVar_hsa_circ_104921,RMVar_hsa_circ_262013,RMVar_hsa_circ_262014,RMVar_hsa_circ_334437,RMVar_hsa_circ_50107,RMVar_hsa_circ_349202,RMVar_hsa_circ_368121,RMVar_hsa_circ_262016 27940 RMVar_ID_27940 Human_SNP_ID_714982534 A-to-I Human chrX + 41101318 41101318 41101318 TTTAGAGAAGCCAGCCAGGCACGGTGGCTCACACCTGTAATTTCAGCACTTTGGGAGGCTTAGGC TTTAGAGAAGCCAGCCAGGCACGGTGGCTCACGCCTGTAATTTCAGCACTTTGGGAGGCTTAGGC A G USP9X Ensembl:ENSG00000124486 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs898102794 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_262025,RMVar_hsa_circ_79754 27941 RMVar_ID_27941 Human_SNP_ID_714982806 A-to-I Human chrX + 41102578 41102578 41102578 CCAGGAGGTGGAGGTTGCAGTGAGTTGAGATCACGCCGCTGGACTCAAGTCTGGGCGACAGAACG CCAGGAGGTGGAGGTTGCAGTGAGTTGAGATCGCGCCGCTGGACTCAAGTCTGGGCGACAGAACG A G USP9X Ensembl:ENSG00000124486 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs960140250 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_262025,RMVar_hsa_circ_79754 27942 RMVar_ID_27942 Human_SNP_ID_714985086 A-to-I Human chrX + 41115100 41115100 41115100 AAAATTAGCCCGGCATTGTGGCACCTGCCTGTAGTCCCAGCTGCTTGGGAGGCTAAGGCAGGAGA AAAATTAGCCCGGCATTGTGGCACCTGCCTGTGGTCCCAGCTGCTTGGGAGGCTAAGGCAGGAGA A G USP9X Ensembl:ENSG00000124486 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs764485382 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_262025,RMVar_hsa_circ_79754 27943 RMVar_ID_27943 Human_SNP_ID_714991953 A-to-I Human chrX + 41151830 41151830 41151830 TGGCGAAACCCCGTCTCTACTGAAAATACAAAAATTAGCCGGGCGTGGTGGCATGCGCCTGTAGT TGGCGAAACCCCGTCTCTACTGAAAATACAAATATTAGCCGGGCGTGGTGGCATGCGCCTGTAGT A T USP9X Ensembl:ENSG00000124486 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs988138330 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_186538,Human_RBP_ID_26275575 RMVar_hsa_circ_270,RMVar_hsa_circ_303204,RMVar_hsa_circ_262025,RMVar_hsa_circ_79754,RMVar_hsa_circ_351557,RMVar_hsa_circ_309268,RMVar_hsa_circ_108335,RMVar_hsa_circ_100863,RMVar_hsa_circ_3212,RMVar_hsa_circ_262026,RMVar_hsa_circ_262028,RMVar_hsa_circ_262029,RMVar_hsa_circ_262027,RMVar_hsa_circ_328854,RMVar_hsa_circ_32339,RMVar_hsa_circ_83083,RMVar_hsa_circ_262043,RMVar_hsa_circ_374068,RMVar_hsa_circ_17416,RMVar_hsa_circ_262048,RMVar_hsa_circ_52167,RMVar_hsa_circ_19972,RMVar_hsa_circ_101464,RMVar_hsa_circ_126978,RMVar_hsa_circ_262050,RMVar_hsa_circ_93087,RMVar_hsa_circ_262052,RMVar_hsa_circ_2216,RMVar_hsa_circ_262053,RMVar_hsa_circ_309396,RMVar_hsa_circ_324868,RMVar_hsa_circ_262051,RMVar_hsa_circ_305050,RMVar_hsa_circ_65747,RMVar_hsa_circ_127136,RMVar_hsa_circ_262057,RMVar_hsa_circ_262059,RMVar_hsa_circ_262058,RMVar_hsa_circ_90733,RMVar_hsa_circ_92022,RMVar_hsa_circ_44851,RMVar_hsa_circ_49524,RMVar_hsa_circ_25932,RMVar_hsa_circ_8384,RMVar_hsa_circ_20355,RMVar_hsa_circ_262060,RMVar_hsa_circ_262062,RMVar_hsa_circ_262064,RMVar_hsa_circ_262063,RMVar_hsa_circ_262061,RMVar_hsa_circ_88531,RMVar_hsa_circ_365510,RMVar_hsa_circ_262066,RMVar_hsa_circ_1087,RMVar_hsa_circ_262067,RMVar_hsa_circ_104656,RMVar_hsa_circ_262068 27944 RMVar_ID_27944 Human_SNP_ID_714999495 A-to-I Human chrX + 41193542 41193542 41193542 AAAAATAAGCCGGGTATGGTGAACATGCCTGTAGTCCCAACTACTCAGGAGGCTAAAGTGGGCAG AAAAATAAGCCGGGTATGGTGAACATGCCTGTGGTCCCAACTACTCAGGAGGCTAAAGTGGGCAG A G USP9X Ensembl:ENSG00000124486 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs753515546 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_270,RMVar_hsa_circ_108335,RMVar_hsa_circ_262026,RMVar_hsa_circ_83083,RMVar_hsa_circ_262043,RMVar_hsa_circ_19972,RMVar_hsa_circ_126978,RMVar_hsa_circ_262051,RMVar_hsa_circ_92022,RMVar_hsa_circ_25932,RMVar_hsa_circ_13260,RMVar_hsa_circ_8384,RMVar_hsa_circ_262060,RMVar_hsa_circ_104656,RMVar_hsa_circ_117496,RMVar_hsa_circ_126498,RMVar_hsa_circ_262068,RMVar_hsa_circ_104080,RMVar_hsa_circ_262072,RMVar_hsa_circ_262073,RMVar_hsa_circ_340852,RMVar_hsa_circ_262074,RMVar_hsa_circ_352939,RMVar_hsa_circ_32979,RMVar_hsa_circ_35250,RMVar_hsa_circ_262080,RMVar_hsa_circ_262084,RMVar_hsa_circ_330850,RMVar_hsa_circ_361473,RMVar_hsa_circ_366735,RMVar_hsa_circ_327049,RMVar_hsa_circ_73338,RMVar_hsa_circ_40695,RMVar_hsa_circ_43261,RMVar_hsa_circ_25611,RMVar_hsa_circ_262086,RMVar_hsa_circ_262087,RMVar_hsa_circ_262085,RMVar_hsa_circ_87841,RMVar_hsa_circ_262083,RMVar_hsa_circ_116006,RMVar_hsa_circ_262092,RMVar_hsa_circ_262094,RMVar_hsa_circ_54106,RMVar_hsa_circ_96543,RMVar_hsa_circ_35450,RMVar_hsa_circ_262095,RMVar_hsa_circ_361463,RMVar_hsa_circ_104462,RMVar_hsa_circ_19673,RMVar_hsa_circ_31705,RMVar_hsa_circ_18250,RMVar_hsa_circ_262098,RMVar_hsa_circ_94308,RMVar_hsa_circ_262099 27945 RMVar_ID_27945 Human_SNP_ID_715001417 A-to-I Human chrX + 41203972 41203972 41203972 CACCCACCTTGGCCTCCCAAAGTGCTGGGATTATAGGCATGAGCCACCATATGCGGCCAAATTTT CACCCACCTTGGCCTCCCAAAGTGCTGGGATTGTAGGCATGAGCCACCATATGCGGCCAAATTTT A G USP9X Ensembl:ENSG00000124486 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388881969 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_270,RMVar_hsa_circ_108335,RMVar_hsa_circ_262026,RMVar_hsa_circ_126978,RMVar_hsa_circ_262051,RMVar_hsa_circ_92022,RMVar_hsa_circ_25932,RMVar_hsa_circ_262060,RMVar_hsa_circ_104656,RMVar_hsa_circ_117496,RMVar_hsa_circ_126498,RMVar_hsa_circ_262068,RMVar_hsa_circ_104080,RMVar_hsa_circ_262072,RMVar_hsa_circ_262073,RMVar_hsa_circ_340852,RMVar_hsa_circ_262074,RMVar_hsa_circ_32979,RMVar_hsa_circ_35250,RMVar_hsa_circ_262084,RMVar_hsa_circ_330850,RMVar_hsa_circ_361473,RMVar_hsa_circ_366735,RMVar_hsa_circ_327049,RMVar_hsa_circ_40695,RMVar_hsa_circ_262086,RMVar_hsa_circ_262085,RMVar_hsa_circ_87841,RMVar_hsa_circ_262083,RMVar_hsa_circ_116006,RMVar_hsa_circ_262092,RMVar_hsa_circ_262094,RMVar_hsa_circ_54106,RMVar_hsa_circ_96543,RMVar_hsa_circ_262095,RMVar_hsa_circ_361463,RMVar_hsa_circ_104462,RMVar_hsa_circ_31705,RMVar_hsa_circ_18250,RMVar_hsa_circ_262098,RMVar_hsa_circ_94308,RMVar_hsa_circ_91237,RMVar_hsa_circ_123062,RMVar_hsa_circ_262099,RMVar_hsa_circ_320680,RMVar_hsa_circ_118439,RMVar_hsa_circ_80797,RMVar_hsa_circ_86446,RMVar_hsa_circ_75963,RMVar_hsa_circ_262103,RMVar_hsa_circ_262105,RMVar_hsa_circ_262104,RMVar_hsa_circ_262101,RMVar_hsa_circ_262102,RMVar_hsa_circ_262100,RMVar_hsa_circ_333759,RMVar_hsa_circ_21673,RMVar_hsa_circ_31795,RMVar_hsa_circ_361359,RMVar_hsa_circ_50345,RMVar_hsa_circ_351902,RMVar_hsa_circ_13418 27946 RMVar_ID_27946 Human_SNP_ID_715016896 A-to-I Human chrX - 41283197 41283197 41283197 AGCGATCCTCCCAAAGTGCTGGGATTCCAGGCATGAGCCATCGCACCTGGCCAGTAGAGCTCTTC AGCGATCCTCCCAAAGTGCTGGGATTCCAGGCGTGAGCCATCGCACCTGGCCAGTAGAGCTCTTC T C lnc-CASK-8,lnc-CASK-8:2,lnc-CASK-8:3,lnc-CASK-8:4 RNACentral:URS0000D5ADD9,RNACentral:URS0000D58911,RNACentral:URS0000D58B56,RNACentral:URS0000D5CA6E lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1020951563 Functional Loss SNV dbSNP153 33..33 33 - - - 27947 RMVar_ID_27947 Human_SNP_ID_715112689 A-to-I Human chrX - 41826588 41826588 41826588 ATGGACCTGTAGTCCCAGCTACTCAGGAGGCTAAGGTGTGAGAATTGCTTGAACCCAGGAGGCAG ATGGACCTGTAGTCCCAGCTACTCAGGAGGCTGAGGTGTGAGAATTGCTTGAACCCAGGAGGCAG T C CASK Ensembl:ENSG00000147044 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1174387684 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_262161,RMVar_hsa_circ_372506,RMVar_hsa_circ_74132 27948 RMVar_ID_27948 Human_SNP_ID_715115680 A-to-I Human chrX - 41843909 41843909 41843909 TGTCTACCAACTGATGAATTTATAAACTAAATATGGTATATCCATACAATGGAATGATTTTTTCA TGTCTACCAACTGATGAATTTATAAACTAAATGTGGTATATCCATACAATGGAATGATTTTTTCA T C CASK Ensembl:ENSG00000147044 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1047875975 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_262161,RMVar_hsa_circ_372506,RMVar_hsa_circ_74132 27949 RMVar_ID_27949 Human_SNP_ID_715483676 A-to-I Human chrX + 44030428 44030428 44030428 TCGTCTTCAGTTAGTGGCAAGACTTGCAGAGGATACAGGTTTGCAGATTCCACCAGCAGCACAGC TCGTCTTCAGTTAGTGGCAAGACTTGCAGAGGGTACAGGTTTGCAGATTCCACCAGCAGCACAGC A G AL034370.1 Ensembl:ENSG00000214019 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879037187 Functional Loss SNV dbSNP153 33..33 33 - - - 27950 RMVar_ID_27950 Human_SNP_ID_715483691 A-to-I Human chrX - 44030510 44030510 44030510 GAAAGTCTTGTTTGCAAATCCATAACAAAAGAAAATTCTGCCACAGCACCAAATGCCAAAGAGCC GAAAGTCTTGTTTGCAAATCCATAACAAAAGAGAATTCTGCCACAGCACCAAATGCCAAAGAGCC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878960481 Functional Loss SNV dbSNP153 33..33 33 - - - 27951 RMVar_ID_27951 Human_SNP_ID_715633498 A-to-I Human chrX + 44871901 44871901 44871901 GTTTATAAACAGAATCTTGTCCTTATATGTCTATCAATTTTTTCCTATCCCTGTTATAAGACATA GTTTATAAACAGAATCTTGTCCTTATATGTCTGTCAATTTTTTCCTATCCCTGTTATAAGACATA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1373451893 Functional Loss SNV dbSNP153 33..33 33 - - - 27952 RMVar_ID_27952 Human_SNP_ID_715634602 A-to-I Human chrX + 44876901 44876877 44876901 ACACACGTGTACATATACATATATACACACGTATACATATACGTATACACACATATACATATACG ACACACGTG________________________TACATATACGTATACACACATATACATATACG GTACATATACATATATACACACGTA G KDM6A Ensembl:ENSG00000147050 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1245505317 Functional Loss DEL dbSNP153 10..33 33 - - - Human_RBP_ID_27793484 RMVar_hsa_circ_35166 27953 RMVar_ID_27953 Human_SNP_ID_715634610 A-to-I Human chrX + 44876893 44876892 44876894 ACATATATACACACGTGTACATATACATATATACACACGTATACATATACGTATACACACATATA ACATATATACACACGTGTACATATACATATAT__ACACGTATACATATACGTATACACACATATA TAC T KDM6A Ensembl:ENSG00000147050 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs199584511 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_27793484 RMVar_hsa_circ_35166 27954 RMVar_ID_27954 Human_SNP_ID_715634690 A-to-I Human chrX + 44877029 44877024 44877030 GTATATACACACGTATACGTGTATACATATATACATGTATATACATACGTATGTATATGCGTATA GTATATACACACGTATACGTGTATACAT______ATGTATATACATACGTATGTATATGCGTATA TATATAC T KDM6A Ensembl:ENSG00000147050 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1472551765 Functional Loss DEL dbSNP153 29..34 33 - - - Human_RBP_ID_17580050 RMVar_hsa_circ_35166 27955 RMVar_ID_27955 Human_SNP_ID_715634691 A-to-I Human chrX + 44877029 44877029 44877029 GTATATACACACGTATACGTGTATACATATATACATGTATATACATACGTATGTATATGCGTATA GTATATACACACGTATACGTGTATACATATATGCATGTATATACATACGTATGTATATGCGTATA A G KDM6A Ensembl:ENSG00000147050 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs891278566 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17580050 RMVar_hsa_circ_35166 27956 RMVar_ID_27956 Human_SNP_ID_715634695 A-to-I Human chrX + 44877039 44877039 44877039 ACGTATACGTGTATACATATATACATGTATATACATACGTATGTATATGCGTATACACATATATG ACGTATACGTGTATACATATATACATGTATATGCATACGTATGTATATGCGTATACACATATATG A G KDM6A Ensembl:ENSG00000147050 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs904733278 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17580050 RMVar_hsa_circ_35166 27957 RMVar_ID_27957 Human_SNP_ID_715634697 A-to-I Human chrX + 44877047 44877044 44877048 GTGTATACATATATACATGTATATACATACGTATGTATATGCGTATACACATATATGTATATATA GTGTATACATATATACATGTATATACATAC____GTATATGCGTATACACATATATGTATATATA CGTAT C KDM6A Ensembl:ENSG00000147050 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs753092811 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_17580050 RMVar_hsa_circ_35166 27958 RMVar_ID_27958 Human_SNP_ID_715634701 A-to-I Human chrX + 44877047 44877047 44877047 GTGTATACATATATACATGTATATACATACGTATGTATATGCGTATACACATATATGTATATATA GTGTATACATATATACATGTATATACATACGTGTGTATATGCGTATACACATATATGTATATATA A G KDM6A Ensembl:ENSG00000147050 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1211919671 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17580050 RMVar_hsa_circ_35166 27959 RMVar_ID_27959 Human_SNP_ID_715636585 A-to-I Human chrX + 44887062 44887062 44887062 GTTCAGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGTGCATGCCACCACTCCTGGTTTTTGTAT GTTCAGCCTCAGCCTCCCGAGTAGCTGGGACTGCAGGTGCATGCCACCACTCCTGGTTTTTGTAT A G KDM6A Ensembl:ENSG00000147050 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1182071867 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35166 27960 RMVar_ID_27960 Human_SNP_ID_715638621 A-to-I Human chrX + 44897592 44897591 44897593 GTGCATCTTGTTCCTTTTTTCTTTTAAGAGACAGGGTCGTGATCAGTCATCCAGACTGGAGTGCA GTGCATCTTGTTCCTTTTTTCTTTTAAGAGAC__GGTCGTGATCAGTCATCCAGACTGGAGTGCA CAG C KDM6A Ensembl:ENSG00000147050 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1201893568 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_8003304,Human_RBP_ID_16889613,Human_RBP_ID_17178335 RMVar_hsa_circ_35166 27961 RMVar_ID_27961 Human_SNP_ID_715638622 A-to-I Human chrX + 44897592 44897592 44897592 GTGCATCTTGTTCCTTTTTTCTTTTAAGAGACAGGGTCGTGATCAGTCATCCAGACTGGAGTGCA GTGCATCTTGTTCCTTTTTTCTTTTAAGAGACTGGGTCGTGATCAGTCATCCAGACTGGAGTGCA A T KDM6A Ensembl:ENSG00000147050 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1036619793 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8003304,Human_RBP_ID_16889613,Human_RBP_ID_17178335 RMVar_hsa_circ_35166 27962 RMVar_ID_27962 Human_SNP_ID_715641483 A-to-I Human chrX + 44912270 44912270 44912270 CCACCATGCCCAGTCAGTTTTTTTGTATTTTTAGTAGAGACGGGTTTCTCCATGTTGGTCAGGCT CCACCATGCCCAGTCAGTTTTTTTGTATTTTTGGTAGAGACGGGTTTCTCCATGTTGGTCAGGCT A G KDM6A Ensembl:ENSG00000147050 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs748840621 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35166 27963 RMVar_ID_27963 Human_SNP_ID_732588930 A-to-I Human chrX + 135434674 135434674 135434674 GGAGGCGGTGCAGGATGGTACACGGGTGCGCCAGGAGCTTGAGCGCAGCCATAAACAGCTAGAGC GGAGGCGGTGCAGGATGGTACACGGGTGCGCCCGGAGCTTGAGCGCAGCCATAAACAGCTAGAGC A C CROCCP1 Ensembl:ENSG00000225769 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1250164385 Functional Loss SNV dbSNP153 33..33 33 - - - 27964 RMVar_ID_27964 Human_SNP_ID_732707036 A-to-I Human chrX - 136217857 136217857 136217857 TAGAGATAGGGTTTTACCATGTTCACCAGGCTAGTCTCGAAATCCTGGCCTCAAGAGATCCACCC TAGAGATAGGGTTTTACCATGTTCACCAGGCTGGTCTCGAAATCCTGGCCTCAAGAGATCCACCC T C MAP7D3 Ensembl:ENSG00000129680 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs1452558781 Functional Loss SNV dbSNP153 33..33 33 - - - 27965 RMVar_ID_27965 Human_SNP_ID_732707041 A-to-I Human chrX - 136217891 136217891 136217891 GCCACCACACCTGGCTAATTTTTTTGTATTTTAGTAGAGATAGGGTTTTACCATGTTCACCAGGC GCCACCACACCTGGCTAATTTTTTTGTATTTTCGTAGAGATAGGGTTTTACCATGTTCACCAGGC T G MAP7D3 Ensembl:ENSG00000129680 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941560867 Functional Loss SNV dbSNP153 33..33 33 - - - 27966 RMVar_ID_27966 Human_SNP_ID_732707046 A-to-I Human chrX - 136217933 136217933 136217933 CTCCTGTCTCAGCCTCCCCAGTAGCTGGGATTACAGGCATGTGCCACCACACCTGGCTAATTTTT CTCCTGTCTCAGCCTCCCCAGTAGCTGGGATTTCAGGCATGTGCCACCACACCTGGCTAATTTTT T A MAP7D3 Ensembl:ENSG00000129680 Protein coding intron GSE38233;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;Bronchiolar epithelium,BERP35T4 cell line - 24183664,31158229 RNA-Seq:(High) rs1420043121 Functional Loss SNV dbSNP153 33..33 33 - - - 27967 RMVar_ID_27967 Human_SNP_ID_732720884 A-to-I Human chrX - 136296354 136296354 136296354 CAAAGGCAGACATCTGGTCCCTGGGCATAACAACTATTTAACTTGCAAAAGGAGAACCACCTTAT CAAAGGCAGACATCTGGTCCCTGGGCATAACAGCTATTTAACTTGCAAAAGGAGAACCACCTTAT T C STK24P1 Ensembl:ENSG00000230079 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1280308231 Functional Loss SNV dbSNP153 33..33 33 - - - 27968 RMVar_ID_27968 Human_SNP_ID_732760143 A-to-I Human chrX + 136510973 136510973 136510973 CAAGGCATTTTTCAGAGCACCCCAGCACATCTAAAATGAATGCTCAAGAAACTGCAACTGGAATG CAAGGCATTTTTCAGAGCACCCCAGCACATCTCAAATGAATGCTCAAGAAACTGCAACTGGAATG A C HTATSF1 Ensembl:ENSG00000102241 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs927676233 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_94773,Human_RBP_ID_5517288,Human_RBP_ID_7980713,Human_RBP_ID_17553110 27969 RMVar_ID_27969 Human_SNP_ID_732815571 A-to-I Human chrX - 136842100 136842100 136842100 AGGATTGCTCGAGCCCAGGAGGTTAAGGCTGCAGTGAGCTATGATCACACCCACTGTACGTCAGT AGGATTGCTCGAGCCCAGGAGGTTAAGGCTGCGGTGAGCTATGATCACACCCACTGTACGTCAGT T C AL683813.2 Ensembl:ENSG00000232611 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1014702011 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16830636 RMVar_hsa_circ_264020 27970 RMVar_ID_27970 Human_SNP_ID_732815572 A-to-I Human chrX - 136842116 136842116 136842116 GGGAGGCTGAGGCAAGAGGATTGCTCGAGCCCAGGAGGTTAAGGCTGCAGTGAGCTATGATCACA GGGAGGCTGAGGCAAGAGGATTGCTCGAGCCCGGGAGGTTAAGGCTGCAGTGAGCTATGATCACA T C AL683813.2 Ensembl:ENSG00000232611 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs3180319 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_264020 27971 RMVar_ID_27971 Human_SNP_ID_732815573 A-to-I Human chrX - 136842116 136842116 136842116 GGGAGGCTGAGGCAAGAGGATTGCTCGAGCCCAGGAGGTTAAGGCTGCAGTGAGCTATGATCACA GGGAGGCTGAGGCAAGAGGATTGCTCGAGCCCCGGAGGTTAAGGCTGCAGTGAGCTATGATCACA T G AL683813.2 Ensembl:ENSG00000232611 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs3180319 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_264020 27972 RMVar_ID_27972 Human_SNP_ID_732815729 A-to-I Human chrX - 136842867 136842867 136842867 GGTTCAAGCGATTCTCCTGTCTCAGCCTCCCAAGTAGCTCTGATTACAGGCATGCGCCACCACGC GGTTCAAGCGATTCTCCTGTCTCAGCCTCCCAGGTAGCTCTGATTACAGGCATGCGCCACCACGC T C AL683813.2 Ensembl:ENSG00000232611 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1273430107 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_264020 27973 RMVar_ID_27973 Human_SNP_ID_732817460 A-to-I Human chrX - 136851088 136851088 136851088 TCTCAGCACTTTGGGAGGATAGCTTGAGGCCTAGGCAACATAGTGAGACCCTGTTTCTATGAAAA TCTCAGCACTTTGGGAGGATAGCTTGAGGCCTGGGCAACATAGTGAGACCCTGTTTCTATGAAAA T C RBMX Ensembl:ENSG00000147274 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1418111953 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16830895 RMVar_hsa_circ_264021 27974 RMVar_ID_27974 Human_SNP_ID_732820518 A-to-I Human chrX - 136863745 136863744 136863746 ATTACTGTAGGGTGTTTTTTTTTTTTAGACACAGTTTTGCTCTTGTCACCCCAGGCTGGAGTGCA ATTACTGTAGGGTGTTTTTTTTTTTTAGACA__GTTTTGCTCTTGTCACCCCAGGCTGGAGTGCA CTG C RBMX Ensembl:ENSG00000147274 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1190482555 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_16831281,Human_RBP_ID_26261022 RMVar_hsa_circ_264021 27975 RMVar_ID_27975 Human_SNP_ID_732832053 A-to-I Human chrX + 136914860 136914860 136914860 GTTGCTCAGGCTGGAGTGCAGTGGCGTGATCTAGCACACTCGAAATCTCCACCACCCAGGTTCAA GTTGCTCAGGCTGGAGTGCAGTGGCGTGATCTGGCACACTCGAAATCTCCACCACCCAGGTTCAA A G AL390879.1 Ensembl:ENSG00000234062 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1466931751 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_264028 27976 RMVar_ID_27976 Human_SNP_ID_732835294 A-to-I Human chrX + 136929485 136929485 136929485 GTGATCCTCCCACCTCAGCCTCCCGAACAGCTAGGACCACGGGCACGCACTACCATGCCCAGCTA GTGATCCTCCCACCTCAGCCTCCCGAACAGCTGGGACCACGGGCACGCACTACCATGCCCAGCTA A G AL390879.1 Ensembl:ENSG00000234062 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1030850670 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_264028 27977 RMVar_ID_27977 Human_SNP_ID_732847079 A-to-I Human chrX + 136990881 136990881 136990881 GTGATCTGCCCACGTTGGCTTCCCAAAGTGCTAGGATTATAGGCATGAGCTACTGCACCCAGGAA GTGATCTGCCCACGTTGGCTTCCCAAAGTGCTGGGATTATAGGCATGAGCTACTGCACCCAGGAA A G AL390879.1 Ensembl:ENSG00000234062 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1471979556 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16832616 27978 RMVar_ID_27978 Human_SNP_ID_733173268 A-to-I Human chrX - 138857681 138857681 138857681 AACTTGAGTTCATTTTGTTATGTGGTGACCACAGTTCTGGATGACGCCCCCCCTGGCACACAGGA AACTTGAGTTCATTTTGTTATGTGGTGACCACCGTTCTGGATGACGCCCCCCCTGGCACACAGGA T G FGF13 Ensembl:ENSG00000129682 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1450482725 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_52778 27979 RMVar_ID_27979 Human_SNP_ID_733348548 A-to-I Human chrX - 139873624 139873624 139873624 TGGCTCGCTGCAGCCTCTGCCTCCCAGGTTCAAGCAATTCTCTGCCTCAGCCTCTTAAGTAGCTG TGGCTCGCTGCAGCCTCTGCCTCCCAGGTTCAGGCAATTCTCTGCCTCAGCCTCTTAAGTAGCTG T C ATP11C Ensembl:ENSG00000101974 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1412561947 Functional Loss SNV dbSNP153 33..33 33 - - - 27980 RMVar_ID_27980 Human_SNP_ID_733351166 A-to-I Human chrX - 139888948 139888948 139888948 TAAAAATTATCTGTGTGTGGCGGTGTGTGCCTATAGTCCCAGCTACTCGGAGGCGGAGGCATGAG TAAAAATTATCTGTGTGTGGCGGTGTGTGCCTGTAGTCCCAGCTACTCGGAGGCGGAGGCATGAG T C ATP11C Ensembl:ENSG00000101974 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1201432032 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26262369 27981 RMVar_ID_27981 Human_SNP_ID_733497071 A-to-I Human chrX - 140723963 140723963 140723963 GTGTATGGAATGTGTGTGTGTATGGAATGGGTAACTGTGCATGTGTATGGAATGTGTGTGTATGG GTGTATGGAATGTGTGTGTGTATGGAATGGGTGACTGTGCATGTGTATGGAATGTGTGTGTATGG T C lnc-CDR1-1,lnc-CDR1-1:2,lnc-CDR1-3 RNACentral:URS00008B1FC3,RNACentral:URS00008BCC8C,RNACentral:URS00008B60B1 lincRNA,lincRNA,lincRNA intron,intron,intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs889086177 Functional Loss SNV dbSNP153 33..33 33 - - - 27982 RMVar_ID_27982 Human_SNP_ID_733497072 A-to-I Human chrX - 140723963 140723963 140723963 GTGTATGGAATGTGTGTGTGTATGGAATGGGTAACTGTGCATGTGTATGGAATGTGTGTGTATGG GTGTATGGAATGTGTGTGTGTATGGAATGGGTCACTGTGCATGTGTATGGAATGTGTGTGTATGG T G lnc-CDR1-1,lnc-CDR1-1:2,lnc-CDR1-3 RNACentral:URS00008B1FC3,RNACentral:URS00008BCC8C,RNACentral:URS00008B60B1 lincRNA,lincRNA,lincRNA intron,intron,intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs889086177 Functional Loss SNV dbSNP153 33..33 33 - - - 27983 RMVar_ID_27983 Human_SNP_ID_733734344 A-to-I Human chrX + 142040131 142040131 142040131 TTCATAGCAGTGTGAAAATGGACTAATATAGTAAACTGGTAGCAGATAGTGGAGTACTGCTGTAA TTCATAGCAGTGTGAAAATGGACTAATATAGTGAACTGGTAGCAGATAGTGGAGTACTGCTGTAA A G AL031073.2 Ensembl:ENSG00000288098 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1326699239 Functional Loss SNV dbSNP153 33..33 33 - - - 27984 RMVar_ID_27984 Human_SNP_ID_733734345 A-to-I Human chrX + 142040139 142040139 142040139 AGTGTGAAAATGGACTAATATAGTAAACTGGTAGCAGATAGTGGAGTACTGCTGTAAAAATTCCT AGTGTGAAAATGGACTAATATAGTAAACTGGTGGCAGATAGTGGAGTACTGCTGTAAAAATTCCT A G AL031073.2 Ensembl:ENSG00000288098 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1405966724 Functional Loss SNV dbSNP153 33..33 33 - - - 27985 RMVar_ID_27985 Human_SNP_ID_733734580 A-to-I Human chrX + 142041543 142041543 142041543 TCCATTTCCCAATAAGTTCCTCTTCTCCATCTAAGACCACCTGAACCTGGACTTCAATGTCCATA TCCATTTCCCAATAAGTTCCTCTTCTCCATCTGAGACCACCTGAACCTGGACTTCAATGTCCATA A G AL031073.2 Ensembl:ENSG00000288098 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1254582644 Functional Loss SNV dbSNP153 33..33 33 - - - 27986 RMVar_ID_27986 Human_SNP_ID_733735638 A-to-I Human chrX + 142047613 142047612 142047613 AATTAACCTCAATAGCAATTCTATTAACTGTTATACAGATCTTATTTAAATTTCACCAATTGCAC AATTAACCTCAATAGCAATTCTATTAACTGTT_TACAGATCTTATTTAAATTTCACCAATTGCAC TA T AL031073.2 Ensembl:ENSG00000288098 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1188632801 Functional Loss DEL dbSNP153 33..33 33 - - - 27987 RMVar_ID_27987 Human_SNP_ID_733777925 A-to-I Human chrX + 142265405 142265405 142265405 AACTTCTCGTTCTGTTCTGTTTCACTCTGATTACTGGTGCATGCAGCCCCTGCCACATGCCCCCT AACTTCTCGTTCTGTTCTGTTTCACTCTGATTGCTGGTGCATGCAGCCCCTGCCACATGCCCCCT A G AL031073.2 Ensembl:ENSG00000288098 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251718209 Functional Loss SNV dbSNP153 33..33 33 - - - 27988 RMVar_ID_27988 Human_SNP_ID_733782590 A-to-I Human chrX + 142288598 142288598 142288598 TATGAAAATGTAAATTAAAGCCACAATGAGATAGCACTTCAGATCCGCTAGGATGGTTAATATTT TATGAAAATGTAAATTAAAGCCACAATGAGATGGCACTTCAGATCCGCTAGGATGGTTAATATTT A G AL031073.2 Ensembl:ENSG00000288098 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1018929016 Functional Loss SNV dbSNP153 33..33 33 - - - 27989 RMVar_ID_27989 Human_SNP_ID_735184220 A-to-I Human chrX + 149948528 149948528 149948528 TAGAAGGCCCTTTCTAGCTCAGGACACATTTGATGCTGTGACTGTTTGGGAATTCAGTCCTGACC TAGAAGGCCCTTTCTAGCTCAGGACACATTTGGTGCTGTGACTGTTTGGGAATTCAGTCCTGACC A G LINC00894 Ensembl:ENSG00000235703 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1557378244 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8277780 RMVar_hsa_circ_281824,RMVar_hsa_circ_306110,RMVar_hsa_circ_42591,RMVar_hsa_circ_341677,RMVar_hsa_circ_70674 27990 RMVar_ID_27990 Human_SNP_ID_735184226 A-to-I Human chrX + 149948566 149948566 149948566 TGACTGTTTGGGAATTCAGTCCTGACCAATTTAAGAGGTTGTGTTTCTTAGCTGTCTCTGGCTCC TGACTGTTTGGGAATTCAGTCCTGACCAATTTGAGAGGTTGTGTTTCTTAGCTGTCTCTGGCTCC A G LINC00894 Ensembl:ENSG00000235703 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1402960871 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_281824,RMVar_hsa_circ_306110,RMVar_hsa_circ_42591,RMVar_hsa_circ_341677,RMVar_hsa_circ_70674 27991 RMVar_ID_27991 Human_SNP_ID_735184444 A-to-I Human chrX + 149949826 149949826 149949826 GAATTAAACTGCGCAAACCAGGAGCCAGAGACAGCTAAGAAACACAACCTCTTAAATTGGTCGGG GAATTAAACTGCGCAAACCAGGAGCCAGAGACCGCTAAGAAACACAACCTCTTAAATTGGTCGGG A C LINC00894 Ensembl:ENSG00000235703 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1294030290 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_281824,RMVar_hsa_circ_306110,RMVar_hsa_circ_42591,RMVar_hsa_circ_341677,RMVar_hsa_circ_70674 27992 RMVar_ID_27992 Human_SNP_ID_51847190 A-to-I Human chr1 + 225397077 225397077 225397077 TTGCCCAGGCTGGAGTGCAGTGGCGTGATCTCAGCTCACTGCAACCTCCGCCTCCTGGGTTCACG TTGCCCAGGCTGGAGTGCAGTGGCGTGATCTCGGCTCACTGCAACCTCCGCCTCCTGGGTTCACG A G DNAH14 Ensembl:ENSG00000185842 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs937528534 Functional Loss SNV dbSNP153 33..33 33 - - - 27993 RMVar_ID_27993 Human_SNP_ID_51847244 A-to-I Human chr1 + 225397237 225397237 225397237 CTGACCTCGTGATCCGCCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCG CTGACCTCGTGATCCGCCCGCCTCAGCCTCCCGAAGTGCTGGGATTACAGGCGTGAGCCACTGCG A G DNAH14 Ensembl:ENSG00000185842 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1267110124 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_102966 27994 RMVar_ID_27994 Human_SNP_ID_51847429 A-to-I Human chr1 + 225397996 225397996 225397996 TGGAACCCAGGCGGTGGAGGTTGCAGTGAGCCAAGATCATGCCACTGCACTCCAGCCTAGGCAAC TGGAACCCAGGCGGTGGAGGTTGCAGTGAGCCGAGATCATGCCACTGCACTCCAGCCTAGGCAAC A G DNAH14 Ensembl:ENSG00000185842 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1251301782 Functional Loss SNV dbSNP153 33..33 33 - - - 27995 RMVar_ID_27995 Human_SNP_ID_51853904 A-to-I Human chr1 - 225423954 225423954 225423954 CGACAGCACCTCCCAGCTTTACACTGTGAAGTATAAAGATGGAACAGAGCTTGAATTGAAAGAGA CGACAGCACCTCCCAGCTTTACACTGTGAAGTGTAAAGATGGAACAGAGCTTGAATTGAAAGAGA T C LBR Ensembl:ENSG00000143815 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1320764205 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1422115,Human_RBP_ID_1738268,Human_RBP_ID_4027705,Human_RBP_ID_5766532,Human_RBP_ID_9491756,Human_RBP_ID_22855889,Human_RBP_ID_26854561,Human_RBP_ID_27176487 Human_Splice_Rec_192453,Human_Splice_Rec_192479,Human_Splice_Rec_192505,Human_Splice_Rec_192541 RMVar_hsa_circ_118468,RMVar_hsa_circ_140023,RMVar_hsa_circ_127091,RMVar_hsa_circ_140034,RMVar_hsa_circ_87052,RMVar_hsa_circ_140035,RMVar_hsa_circ_352875 27996 RMVar_ID_27996 Human_SNP_ID_51858495 A-to-I Human chr1 - 225442799 225442799 225442799 TTGCCCAGGCTGGAGTGCAGTGGCGTGATCTCAGCTCACTGCAACATCTGCCTCCCGGGTTCACA TTGCCCAGGCTGGAGTGCAGTGGCGTGATCTCGGCTCACTGCAACATCTGCCTCCCGGGTTCACA T C LINC02765 RNACentral:URS0000D5CE19 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1456524506 Functional Loss SNV dbSNP153 33..33 33 - - - 27997 RMVar_ID_27997 Human_SNP_ID_51870610 A-to-I Human chr1 - 225492210 225492210 225492210 ATGGTGGTGCACACCTGTAATCCCAGCTACTCAGGAGACTGAAGCGGGAGGATCACCTGAGCCCA ATGGTGGTGCACACCTGTAATCCCAGCTACTCGGGAGACTGAAGCGGGAGGATCACCTGAGCCCA T C ENAH Ensembl:ENSG00000154380 Protein coding 3'UTR GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs905096174 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_140038,RMVar_hsa_circ_78634,RMVar_hsa_circ_112222,RMVar_hsa_circ_140039 27998 RMVar_ID_27998 Human_SNP_ID_51871854 A-to-I Human chr1 - 225497655 225497651 225497655 TTATGAGCTGTAAGAAGAAAATGGAGACAAACAGAAGGAGGGAAAAACCAACCTACTCTGAAAGC TTATGAGCTGTAAGAAGAAAATGGAGACAAAC____GGAGGGAAAAACCAACCTACTCTGAAAGC CTTCT C ENAH Ensembl:ENSG00000154380 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1407843614 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_1738313,Human_RBP_ID_9357571,Human_RBP_ID_18564424,Human_RBP_ID_22782350,Human_RBP_ID_26854615,Human_RBP_ID_27176551 RMVar_hsa_circ_140038,RMVar_hsa_circ_78634,RMVar_hsa_circ_112222,RMVar_hsa_circ_140039 27999 RMVar_ID_27999 Human_SNP_ID_51898851 A-to-I Human chr1 - 225609767 225609767 225609767 CCCAGATACTCAGGAGGCTGGGCATGAGAACCACTTGAACCTGAGAGGTGGATGTTGCAGTGAGC CCCAGATACTCAGGAGGCTGGGCATGAGAACCGCTTGAACCTGAGAGGTGGATGTTGCAGTGAGC T C ENAH Ensembl:ENSG00000154380 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1245227314 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10805934 RMVar_hsa_circ_140038,RMVar_hsa_circ_78634,RMVar_hsa_circ_94840,RMVar_hsa_circ_140044 28000 RMVar_ID_28000 Human_SNP_ID_51902911 A-to-I Human chr1 - 225625577 225625577 225625577 TGGAGGTTGGGGTGAGCTGAGATCATGTCATTACACTGCAGCCTGGGCAACAAGAGCGAAATTCC TGGAGGTTGGGGTGAGCTGAGATCATGTCATTGCACTGCAGCCTGGGCAACAAGAGCGAAATTCC T C ENAH Ensembl:ENSG00000154380 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs547839440 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_140038,RMVar_hsa_circ_78634,RMVar_hsa_circ_94840,RMVar_hsa_circ_140044 28001 RMVar_ID_28001 Human_SNP_ID_51902923 A-to-I Human chr1 - 225625654 225625654 225625654 ACAATTAGCCGGGCACGTTGGCACATGCCTGTAATCCTAGCTAGTTGGGAGGCTGAGAATCGCTT ACAATTAGCCGGGCACGTTGGCACATGCCTGTGATCCTAGCTAGTTGGGAGGCTGAGAATCGCTT T C ENAH Ensembl:ENSG00000154380 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1402390613 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_140038,RMVar_hsa_circ_78634,RMVar_hsa_circ_94840,RMVar_hsa_circ_140044 28002 RMVar_ID_28002 Human_SNP_ID_51905712 A-to-I Human chr1 - 225637866 225637866 225637866 CAGGCTGAAATGCAGTGGCGCGATCATAGCTCACTGCAACCTGGAACTCCTGGGCTCAAGCCATC CAGGCTGAAATGCAGTGGCGCGATCATAGCTCGCTGCAACCTGGAACTCCTGGGCTCAAGCCATC T C ENAH Ensembl:ENSG00000154380 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs960957601 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_97980 RMVar_hsa_circ_140038,RMVar_hsa_circ_78634,RMVar_hsa_circ_94840,RMVar_hsa_circ_140044 28003 RMVar_ID_28003 Human_SNP_ID_51905808 A-to-I Human chr1 - 225638297 225638297 225638297 AATATTAGCTGGGTGTGGTGGTGCACACCTGTAGTCCTAGCTATACTCAGGAGATTGAGGTAGGA AATATTAGCTGGGTGTGGTGGTGCACACCTGTGGTCCTAGCTATACTCAGGAGATTGAGGTAGGA T C ENAH Ensembl:ENSG00000154380 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs960924794 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2126946,Human_RBP_ID_10806820 RMVar_hsa_circ_140038,RMVar_hsa_circ_78634,RMVar_hsa_circ_94840,RMVar_hsa_circ_140044 28004 RMVar_ID_28004 Human_SNP_ID_51906485 A-to-I Human chr1 - 225641047 225641047 225641047 CATCCTGGCTAACACGGTGAAACCCTGTCTCTACTAAAAATACAAAAAATTAGTCAGGCGTGGTG CATCCTGGCTAACACGGTGAAACCCTGTCTCTGCTAAAAATACAAAAAATTAGTCAGGCGTGGTG T C ENAH Ensembl:ENSG00000154380 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1186811672 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_140038,RMVar_hsa_circ_78634,RMVar_hsa_circ_94840,RMVar_hsa_circ_140044 28005 RMVar_ID_28005 Human_SNP_ID_51941788 A-to-I Human chr1 + 225784663 225784663 225784663 GGAGATCGAGACCATCCTGGCTAACACGGTGAAACCCCATCTCTACTAAAAATACAAAAAAATTA GGAGATCGAGACCATCCTGGCTAACACGGTGACACCCCATCTCTACTAAAAATACAAAAAAATTA A C SRP9 Ensembl:ENSG00000143742 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1438415842 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35495,RMVar_hsa_circ_100395,RMVar_hsa_circ_140051 28006 RMVar_ID_28006 Human_SNP_ID_51941933 A-to-I Human chr1 + 225785210 225785210 225785210 CTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGCCGTGCACCACCACGCCCAACTAATTTTT CTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTGCAGCCGTGCACCACCACGCCCAACTAATTTTT A G SRP9 Ensembl:ENSG00000143742 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs951080308 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35495,RMVar_hsa_circ_100395,RMVar_hsa_circ_140051 28007 RMVar_ID_28007 Human_SNP_ID_51941972 A-to-I Human chr1 + 225785279 225785279 225785279 TTTTTTTTTTTAGTAGAGACGGGGTTTTCACCATGTTGACCAGGATGGTCTCCATCTCTTTACCT TTTTTTTTTTTAGTAGAGACGGGGTTTTCACCGTGTTGACCAGGATGGTCTCCATCTCTTTACCT A G SRP9 Ensembl:ENSG00000143742 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1318907812 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35495,RMVar_hsa_circ_100395,RMVar_hsa_circ_140051 28008 RMVar_ID_28008 Human_SNP_ID_51942448 A-to-I Human chr1 + 225786860 225786860 225786860 GATTGGTTGGTTGATTGCTTTTTTTTTTTTTTAGAGACAGTGTCTTGCTCTATTGCTCAGGCTGC GATTGGTTGGTTGATTGCTTTTTTTTTTTTTTGGAGACAGTGTCTTGCTCTATTGCTCAGGCTGC A G SRP9 Ensembl:ENSG00000143742 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1456377906 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5767816,Human_RBP_ID_10807868 RMVar_hsa_circ_35495,RMVar_hsa_circ_100395,RMVar_hsa_circ_140051,RMVar_hsa_circ_84583 28009 RMVar_ID_28009 Human_SNP_ID_51942449 A-to-I Human chr1 + 225786860 225786860 225786860 GATTGGTTGGTTGATTGCTTTTTTTTTTTTTTAGAGACAGTGTCTTGCTCTATTGCTCAGGCTGC GATTGGTTGGTTGATTGCTTTTTTTTTTTTTTTGAGACAGTGTCTTGCTCTATTGCTCAGGCTGC A T SRP9 Ensembl:ENSG00000143742 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1456377906 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_5767816,Human_RBP_ID_10807868 RMVar_hsa_circ_35495,RMVar_hsa_circ_100395,RMVar_hsa_circ_140051,RMVar_hsa_circ_84583 28010 RMVar_ID_28010 Human_SNP_ID_51942457 A-to-I Human chr1 + 225786879 225786877 225786879 TTTTTTTTTTTTTAGAGACAGTGTCTTGCTCTATTGCTCAGGCTGCAGTGCAGTGGCATGATCAT TTTTTTTTTTTTTAGAGACAGTGTCTTGCTC__TTGCTCAGGCTGCAGTGCAGTGGCATGATCAT CTA C SRP9 Ensembl:ENSG00000143742 Protein coding CDS GSE38233;GSE56152;GSE100210 cultured B-cells;embryonic stem cells,wild type;HepG2 cell line - 24183664,25708366,29129909 RNA-Seq:(High) rs1559006386 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_10807870,Human_RBP_ID_17557432,Human_RBP_ID_23368629 Human_Splice_Rec_192742,Human_Splice_Rec_192758,Human_Splice_Rec_192764,Human_Splice_Rec_192776 Human_miRNA_ID_2577930,Human_miRNA_ID_2676647 RMVar_hsa_circ_35495,RMVar_hsa_circ_100395,RMVar_hsa_circ_140051,RMVar_hsa_circ_140054,RMVar_hsa_circ_84583 28011 RMVar_ID_28011 Human_SNP_ID_51942458 A-to-I Human chr1 + 225786879 225786879 225786879 TTTTTTTTTTTTTAGAGACAGTGTCTTGCTCTATTGCTCAGGCTGCAGTGCAGTGGCATGATCAT TTTTTTTTTTTTTAGAGACAGTGTCTTGCTCTGTTGCTCAGGCTGCAGTGCAGTGGCATGATCAT A G SRP9 Ensembl:ENSG00000143742 Protein coding CDS GSE38233;GSE56152;GSE100210 cultured B-cells;embryonic stem cells,wild type;HepG2 cell line - 24183664,25708366,29129909 RNA-Seq:(High) rs1161553517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10807870,Human_RBP_ID_17557432,Human_RBP_ID_23368629 Human_Splice_Rec_192742,Human_Splice_Rec_192758,Human_Splice_Rec_192764,Human_Splice_Rec_192776 Human_miRNA_ID_2577930,Human_miRNA_ID_2676647 RMVar_hsa_circ_35495,RMVar_hsa_circ_100395,RMVar_hsa_circ_140051,RMVar_hsa_circ_140054,RMVar_hsa_circ_84583 28012 RMVar_ID_28012 Human_SNP_ID_51942459 A-to-I Human chr1 + 225786879 225786879 225786879 TTTTTTTTTTTTTAGAGACAGTGTCTTGCTCTATTGCTCAGGCTGCAGTGCAGTGGCATGATCAT TTTTTTTTTTTTTAGAGACAGTGTCTTGCTCTTTTGCTCAGGCTGCAGTGCAGTGGCATGATCAT A T SRP9 Ensembl:ENSG00000143742 Protein coding CDS GSE38233;GSE56152;GSE100210 cultured B-cells;embryonic stem cells,wild type;HepG2 cell line - 24183664,25708366,29129909 RNA-Seq:(High) rs1161553517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10807870,Human_RBP_ID_17557432,Human_RBP_ID_23368629 Human_Splice_Rec_192742,Human_Splice_Rec_192758,Human_Splice_Rec_192764,Human_Splice_Rec_192776 Human_miRNA_ID_2577930,Human_miRNA_ID_2676647 RMVar_hsa_circ_35495,RMVar_hsa_circ_100395,RMVar_hsa_circ_140051,RMVar_hsa_circ_140054,RMVar_hsa_circ_84583 28013 RMVar_ID_28013 Human_SNP_ID_51942467 A-to-I Human chr1 + 225786898 225786898 225786898 AGTGTCTTGCTCTATTGCTCAGGCTGCAGTGCAGTGGCATGATCATAGCTCACTGCATCCTCGAC AGTGTCTTGCTCTATTGCTCAGGCTGCAGTGCGGTGGCATGATCATAGCTCACTGCATCCTCGAC A G SRP9 Ensembl:ENSG00000143742 Protein coding CDS GSE56152;GSE100210 embryonic stem cells,wild type;HepG2 cell line - 25708366,29129909 RNA-Seq:(High) rs753429237 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557432,Human_RBP_ID_23368629 Human_Splice_Rec_192742,Human_Splice_Rec_192758,Human_Splice_Rec_192759,Human_Splice_Rec_192764,Human_Splice_Rec_192765,Human_Splice_Rec_192776 RMVar_hsa_circ_35495,RMVar_hsa_circ_100395,RMVar_hsa_circ_140051,RMVar_hsa_circ_140054,RMVar_hsa_circ_84583 28014 RMVar_ID_28014 Human_SNP_ID_51942469 A-to-I Human chr1 + 225786912 225786912 225786912 TTGCTCAGGCTGCAGTGCAGTGGCATGATCATAGCTCACTGCATCCTCGACCTCCTGGGCTCAAG TTGCTCAGGCTGCAGTGCAGTGGCATGATCATGGCTCACTGCATCCTCGACCTCCTGGGCTCAAG A G SRP9 Ensembl:ENSG00000143742 Protein coding CDS GSE56152;GSE100210 embryonic stem cells,wild type;HepG2 cell line - 25708366,29129909 RNA-Seq:(High) rs1130901 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4027995,Human_RBP_ID_17557432 Human_Splice_Rec_192742,Human_Splice_Rec_192758,Human_Splice_Rec_192759,Human_Splice_Rec_192764,Human_Splice_Rec_192765,Human_Splice_Rec_192776 Human_miRNA_ID_2465610 RMVar_hsa_circ_35495,RMVar_hsa_circ_100395,RMVar_hsa_circ_140051,RMVar_hsa_circ_140054,RMVar_hsa_circ_84583 28015 RMVar_ID_28015 Human_SNP_ID_51942499 A-to-I Human chr1 + 225786975 225786975 225786975 AGCGGTCCTCTTGCTTCAGCCTCCTGAATAGCAGAGACTACAGGTGTGCACCACCACACTCAGCT AGCGGTCCTCTTGCTTCAGCCTCCTGAATAGCTGAGACTACAGGTGTGCACCACCACACTCAGCT A T SRP9 Ensembl:ENSG00000143742 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1173564787 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_222314,Human_RBP_ID_5767818,Human_RBP_ID_17557433,Human_RBP_ID_24647309 Human_Splice_Rec_192759,Human_Splice_Rec_192765 RMVar_hsa_circ_35495,RMVar_hsa_circ_100395,RMVar_hsa_circ_140051,RMVar_hsa_circ_140054,RMVar_hsa_circ_84583 28016 RMVar_ID_28016 Human_SNP_ID_51942589 A-to-I Human chr1 + 225787315 225787315 225787315 CCAGCATTTTGGGAGGCTGAGGTGGGCGGATCATGAGGTCAGGAGTTCGAGACCAGCCTGACCAA CCAGCATTTTGGGAGGCTGAGGTGGGCGGATCGTGAGGTCAGGAGTTCGAGACCAGCCTGACCAA A G SRP9 Ensembl:ENSG00000143742 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1224563502 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_140054,RMVar_hsa_circ_84583 28017 RMVar_ID_28017 Human_SNP_ID_51942616 A-to-I Human chr1 + 225787407 225787407 225787407 ATACAAATATTAGCATGGTGGTGGGTGCCTGTAATCTCAGCTACTTGGGAGGCTGAGGCAGGAGA ATACAAATATTAGCATGGTGGTGGGTGCCTGTGATCTCAGCTACTTGGGAGGCTGAGGCAGGAGA A G SRP9 Ensembl:ENSG00000143742 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229,31158229 RNA-Seq:(High) rs954669341 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_140054,RMVar_hsa_circ_84583 28018 RMVar_ID_28018 Human_SNP_ID_51942805 A-to-I Human chr1 + 225788198 225788198 225788198 AGAATTTGGTTTGATTTAAAAGTAATATCTTCAAGCCTGGGCAACATGGAGAAACCCCGTCTCTA AGAATTTGGTTTGATTTAAAAGTAATATCTTCCAGCCTGGGCAACATGGAGAAACCCCGTCTCTA A C SRP9 Ensembl:ENSG00000143742 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1314755526 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2127076,Human_RBP_ID_5767837,Human_RBP_ID_10807925,Human_RBP_ID_22856050,Human_RBP_ID_26376197 RMVar_hsa_circ_140054,RMVar_hsa_circ_84583 28019 RMVar_ID_28019 Human_SNP_ID_51942809 A-to-I Human chr1 + 225788211 225788211 225788211 ATTTAAAAGTAATATCTTCAAGCCTGGGCAACATGGAGAAACCCCGTCTCTACTAAAAATAGAAA ATTTAAAAGTAATATCTTCAAGCCTGGGCAACTTGGAGAAACCCCGTCTCTACTAAAAATAGAAA A T SRP9 Ensembl:ENSG00000143742 Protein coding intron GSE38233;GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,32596459 RNA-Seq:(High) rs1364158923 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5767837,Human_RBP_ID_26389152 RMVar_hsa_circ_140054,RMVar_hsa_circ_84583 28020 RMVar_ID_28020 Human_SNP_ID_51942835 A-to-I Human chr1 + 225788313 225788313 225788313 GCTACTCAGGAAGCTGAGGATCGCTTGAGCCCAGGACGCAGGTTGCAGTGAGCTGAGATTGCACC GCTACTCAGGAAGCTGAGGATCGCTTGAGCCCGGGACGCAGGTTGCAGTGAGCTGAGATTGCACC A G SRP9 Ensembl:ENSG00000143742 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs897456724 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_343619,Human_RBP_ID_1253313,Human_RBP_ID_5767839,Human_RBP_ID_10807926,Human_RBP_ID_26386932 RMVar_hsa_circ_140054,RMVar_hsa_circ_84583 28021 RMVar_ID_28021 Human_SNP_ID_51942837 A-to-I Human chr1 + 225788327 225788327 225788327 TGAGGATCGCTTGAGCCCAGGACGCAGGTTGCAGTGAGCTGAGATTGCACCACTACACCCCCAAC TGAGGATCGCTTGAGCCCAGGACGCAGGTTGCCGTGAGCTGAGATTGCACCACTACACCCCCAAC A C SRP9 Ensembl:ENSG00000143742 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs573068399 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_343619,Human_RBP_ID_1253313,Human_RBP_ID_5767839,Human_RBP_ID_10807928,Human_RBP_ID_26386932 RMVar_hsa_circ_140054,RMVar_hsa_circ_84583 28022 RMVar_ID_28022 Human_SNP_ID_51942840 A-to-I Human chr1 + 225788349 225788349 225788349 CGCAGGTTGCAGTGAGCTGAGATTGCACCACTACACCCCCAACCTGGGCCACAGAGTGAGACACT CGCAGGTTGCAGTGAGCTGAGATTGCACCACTGCACCCCCAACCTGGGCCACAGAGTGAGACACT A G SRP9 Ensembl:ENSG00000143742 Protein coding intron GSE100210;GSE99789;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,29796672,31158229,31158229 RNA-Seq:(High) rs1304974062 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5767843,Human_RBP_ID_9492869,Human_RBP_ID_23147254,Human_RBP_ID_24759266,Human_RBP_ID_26376198 RMVar_hsa_circ_140054,RMVar_hsa_circ_84583 28023 RMVar_ID_28023 Human_SNP_ID_51942885 A-to-I Human chr1 + 225788472 225788464 225788472 GGAATCTCACTCTGTCGCCCAGGCTGGAGTGCAGTGGCATGATCTTGGCTCACTGCAGCCCTCAC GGAATCTCACTCTGTCGCCCAGGCT________GTGGCATGATCTTGGCTCACTGCAGCCCTCAC TGGAGTGCA T SRP9 Ensembl:ENSG00000143742 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,31158229,32596459 RNA-Seq:(High) rs1265210242 Functional Loss DEL dbSNP153 26..33 33 - - - RMVar_hsa_circ_140054,RMVar_hsa_circ_84583 28024 RMVar_ID_28024 Human_SNP_ID_51942888 A-to-I Human chr1 + 225788472 225788472 225788472 GGAATCTCACTCTGTCGCCCAGGCTGGAGTGCAGTGGCATGATCTTGGCTCACTGCAGCCCTCAC GGAATCTCACTCTGTCGCCCAGGCTGGAGTGCCGTGGCATGATCTTGGCTCACTGCAGCCCTCAC A C SRP9 Ensembl:ENSG00000143742 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,31158229,32596459 RNA-Seq:(High) rs1289588897 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_140054,RMVar_hsa_circ_84583 28025 RMVar_ID_28025 Human_SNP_ID_51942893 A-to-I Human chr1 + 225788496 225788496 225788496 TGGAGTGCAGTGGCATGATCTTGGCTCACTGCAGCCCTCACTCCTGGGTTCAAGCGATTCTCCTG TGGAGTGCAGTGGCATGATCTTGGCTCACTGCGGCCCTCACTCCTGGGTTCAAGCGATTCTCCTG A G SRP9 Ensembl:ENSG00000143742 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,31158229,32596459 RNA-Seq:(High) rs936196989 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5767847 RMVar_hsa_circ_140054,RMVar_hsa_circ_84583 28026 RMVar_ID_28026 Human_SNP_ID_51942903 A-to-I Human chr1 + 225788533 225788533 225788533 TCACTCCTGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTAAGTAGCTGGGATTACAGGCACACG TCACTCCTGGGTTCAAGCGATTCTCCTGCCTCGGCCTCCTAAGTAGCTGGGATTACAGGCACACG A G SRP9 Ensembl:ENSG00000143742 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs548401730 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_140054,RMVar_hsa_circ_84583 28027 RMVar_ID_28027 Human_SNP_ID_51959992 A-to-I Human chr1 - 225851455 225851455 225851455 TGAGGTAGGAGAATCACTTGAACTCAGGAGGCAGAGGTTGCAGTGAGCCAAGATTGCACCAGTGC TGAGGTAGGAGAATCACTTGAACTCAGGAGGCGGAGGTTGCAGTGAGCCAAGATTGCACCAGTGC T C TMEM63A Ensembl:ENSG00000196187 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1048688101 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58675,RMVar_hsa_circ_121882,RMVar_hsa_circ_140059 28028 RMVar_ID_28028 Human_SNP_ID_51963162 A-to-I Human chr1 - 225863132 225863132 225863132 GGAGGATTGATTGAGCCCAGAAGGTTGAGGCTACAGTGAGCCATGATTGTGCCACTGTACAGCAG GGAGGATTGATTGAGCCCAGAAGGTTGAGGCTTCAGTGAGCCATGATTGTGCCACTGTACAGCAG T A TMEM63A Ensembl:ENSG00000196187 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs360082 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2800,GWAS_ID_2801,GWAS_ID_2802,GWAS_ID_2803,GWAS_ID_2804 RMVar_hsa_circ_55460,RMVar_hsa_circ_23341,RMVar_hsa_circ_77294,RMVar_hsa_circ_33471,RMVar_hsa_circ_349997,RMVar_hsa_circ_80737,RMVar_hsa_circ_140060,RMVar_hsa_circ_140061 28029 RMVar_ID_28029 Human_SNP_ID_51963163 A-to-I Human chr1 - 225863132 225863132 225863132 GGAGGATTGATTGAGCCCAGAAGGTTGAGGCTACAGTGAGCCATGATTGTGCCACTGTACAGCAG GGAGGATTGATTGAGCCCAGAAGGTTGAGGCTGCAGTGAGCCATGATTGTGCCACTGTACAGCAG T C TMEM63A Ensembl:ENSG00000196187 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs360082 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2800,GWAS_ID_2801,GWAS_ID_2802,GWAS_ID_2803,GWAS_ID_2804 RMVar_hsa_circ_55460,RMVar_hsa_circ_23341,RMVar_hsa_circ_77294,RMVar_hsa_circ_33471,RMVar_hsa_circ_349997,RMVar_hsa_circ_80737,RMVar_hsa_circ_140060,RMVar_hsa_circ_140061 28030 RMVar_ID_28030 Human_SNP_ID_51963164 A-to-I Human chr1 - 225863137 225863137 225863137 AGGTGGGAGGATTGATTGAGCCCAGAAGGTTGAGGCTACAGTGAGCCATGATTGTGCCACTGTAC AGGTGGGAGGATTGATTGAGCCCAGAAGGTTGGGGCTACAGTGAGCCATGATTGTGCCACTGTAC T C TMEM63A Ensembl:ENSG00000196187 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs977939722 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55460,RMVar_hsa_circ_23341,RMVar_hsa_circ_77294,RMVar_hsa_circ_33471,RMVar_hsa_circ_349997,RMVar_hsa_circ_80737,RMVar_hsa_circ_140060,RMVar_hsa_circ_140061 28031 RMVar_ID_28031 Human_SNP_ID_51963166 A-to-I Human chr1 - 225863146 225863146 225863146 AGGAGGCTGAGGTGGGAGGATTGATTGAGCCCAGAAGGTTGAGGCTACAGTGAGCCATGATTGTG AGGAGGCTGAGGTGGGAGGATTGATTGAGCCCCGAAGGTTGAGGCTACAGTGAGCCATGATTGTG T G TMEM63A Ensembl:ENSG00000196187 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1347720821 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55460,RMVar_hsa_circ_23341,RMVar_hsa_circ_77294,RMVar_hsa_circ_33471,RMVar_hsa_circ_349997,RMVar_hsa_circ_80737,RMVar_hsa_circ_140060,RMVar_hsa_circ_140061 28032 RMVar_ID_28032 Human_SNP_ID_51963189 A-to-I Human chr1 - 225863246 225863246 225863246 GGCCAGAAGTTCGAAATCAGCCTGGGCAACATAGCGAGACCCCGTCTCTACAAAAAATAAAAATC GGCCAGAAGTTCGAAATCAGCCTGGGCAACATTGCGAGACCCCGTCTCTACAAAAAATAAAAATC T A TMEM63A Ensembl:ENSG00000196187 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs888663225 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_98982 RMVar_hsa_circ_55460,RMVar_hsa_circ_23341,RMVar_hsa_circ_77294,RMVar_hsa_circ_33471,RMVar_hsa_circ_349997,RMVar_hsa_circ_80737,RMVar_hsa_circ_140060,RMVar_hsa_circ_140061 28033 RMVar_ID_28033 Human_SNP_ID_51963205 A-to-I Human chr1 - 225863322 225863322 225863322 AAAAGGCTAGCGGGGTGCAGTGACTCACGCCTACAATCCCAGCACTTTGGGAGGGTGAGACAGGA AAAAGGCTAGCGGGGTGCAGTGACTCACGCCTGCAATCCCAGCACTTTGGGAGGGTGAGACAGGA T C TMEM63A Ensembl:ENSG00000196187 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs960341853 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_825,Human_RBP_ID_98982,Human_RBP_ID_24647490 RMVar_hsa_circ_55460,RMVar_hsa_circ_23341,RMVar_hsa_circ_77294,RMVar_hsa_circ_33471,RMVar_hsa_circ_349997,RMVar_hsa_circ_80737,RMVar_hsa_circ_140060,RMVar_hsa_circ_140061 28034 RMVar_ID_28034 Human_SNP_ID_51963621 A-to-I Human chr1 - 225865012 225865012 225865012 GACTTAAGGCATCTTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTGCAGACACATGGCACCACAC GACTTAAGGCATCTTCCTGCCTCAGCCTCCCAGGTAGCTGGGACTGCAGACACATGGCACCACAC T C TMEM63A Ensembl:ENSG00000196187 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs774638417 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55460,RMVar_hsa_circ_23341,RMVar_hsa_circ_77294,RMVar_hsa_circ_33471,RMVar_hsa_circ_349997,RMVar_hsa_circ_80737,RMVar_hsa_circ_140060,RMVar_hsa_circ_140061 28035 RMVar_ID_28035 Human_SNP_ID_51964827 A-to-I Human chr1 - 225869731 225869731 225869731 TTGAAACCGGAAGGCGGAGGTCGCAGTGAGCCAAGATCACCCCACTGCAACTCCAGCCTGAGTGA TTGAAACCGGAAGGCGGAGGTCGCAGTGAGCCGAGATCACCCCACTGCAACTCCAGCCTGAGTGA T C TMEM63A Ensembl:ENSG00000196187 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs967470770 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55460,RMVar_hsa_circ_77294,RMVar_hsa_circ_33471,RMVar_hsa_circ_104024,RMVar_hsa_circ_140061,RMVar_hsa_circ_120656,RMVar_hsa_circ_94798,RMVar_hsa_circ_140062,RMVar_hsa_circ_140063,RMVar_hsa_circ_140064,RMVar_hsa_circ_140066,RMVar_hsa_circ_98200 28036 RMVar_ID_28036 Human_SNP_ID_51993824 A-to-I Human chr1 - 225979515 225979515 225979515 TTTCAGTCATTAAAAAGTACAAAGAATTAGCCAGGTGTGGTTGTGCGTGCCTATAGTTCCAGCTA TTTCAGTCATTAAAAAGTACAAAGAATTAGCCGGGTGTGGTTGTGCGTGCCTATAGTTCCAGCTA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1344395313 Functional Loss SNV dbSNP153 33..33 33 - - - 28037 RMVar_ID_28037 Human_SNP_ID_51995987 A-to-I Human chr1 - 225988159 225988159 225988159 AACAACTGCAGATCCCGGTGACTGACTCTGGGAGGCATATTTTAGAAGACTCATGTGCTGAGCTG AACAACTGCAGATCCCGGTGACTGACTCTGGGCGGCATATTTTAGAAGACTCATGTGCTGAGCTG T G SDE2 Ensembl:ENSG00000143751 Protein coding CDS GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs746943280 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_975391,Human_RBP_ID_1422404,Human_RBP_ID_5768481,Human_RBP_ID_8744113,Human_RBP_ID_10810013,Human_RBP_ID_17676753,Human_RBP_ID_17740906,Human_RBP_ID_18225225,Human_RBP_ID_24541372,Human_RBP_ID_27588466 Human_miRNA_ID_2946714 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 28038 RMVar_ID_28038 Human_SNP_ID_51997885 A-to-I Human chr1 - 225995008 225995008 225995008 ACACTGCCTTGTTTTGTCGCCCAGGCTGGAGTACAGTGGTACGATCACGGCTCACTGCAGCTTTG ACACTGCCTTGTTTTGTCGCCCAGGCTGGAGTGCAGTGGTACGATCACGGCTCACTGCAGCTTTG T C SDE2 Ensembl:ENSG00000143751 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs747277093 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19288133 RMVar_hsa_circ_45926,RMVar_hsa_circ_109300,RMVar_hsa_circ_140078,RMVar_hsa_circ_70142 28039 RMVar_ID_28039 Human_SNP_ID_51998517 A-to-I Human chr1 - 225997697 225997697 225997697 GCCAGGCGTGGTGGCTCACGCCTGTAATTCCAACACTTAGGGAGGTCGAGGCGGGCAGATCACCT GCCAGGCGTGGTGGCTCACGCCTGTAATTCCAGCACTTAGGGAGGTCGAGGCGGGCAGATCACCT T C SDE2 Ensembl:ENSG00000143751 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs928166497 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109300,RMVar_hsa_circ_140078 28040 RMVar_ID_28040 Human_SNP_ID_51998528 A-to-I Human chr1 - 225997726 225997726 225997726 AATTTTTAAATCGGAAGCAAGAAATATAGGCCAGGCGTGGTGGCTCACGCCTGTAATTCCAACAC AATTTTTAAATCGGAAGCAAGAAATATAGGCCGGGCGTGGTGGCTCACGCCTGTAATTCCAACAC T C SDE2 Ensembl:ENSG00000143751 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1003916931 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109300,RMVar_hsa_circ_140078 28041 RMVar_ID_28041 Human_SNP_ID_51998579 A-to-I Human chr1 - 225997887 225997887 225997887 ACCTCGGGTGATCCGCCCACCTCAGCCTCACAAAGTGCTGGGATTACAGGCTTGAGCCACTCCTC ACCTCGGGTGATCCGCCCACCTCAGCCTCACAGAGTGCTGGGATTACAGGCTTGAGCCACTCCTC T C SDE2 Ensembl:ENSG00000143751 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs538918670 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109300,RMVar_hsa_circ_140078 28042 RMVar_ID_28042 Human_SNP_ID_52002245 A-to-I Human chr1 - 226012474 226012474 226012474 TTTGAGACGGCTGTCGCCCAGGCTGGAGTGCAATGGCGCGATCTCGGCTCATTGCAAACTCCGCC TTTGAGACGGCTGTCGCCCAGGCTGGAGTGCAGTGGCGCGATCTCGGCTCATTGCAAACTCCGCC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1341946701 Functional Loss SNV dbSNP153 33..33 33 - - - 28043 RMVar_ID_28043 Human_SNP_ID_52013166 A-to-I Human chr1 - 226057272 226057271 226057273 TTTTCCATTACTATTTTTTCTTTTTTTGAGACAGAGTCTCACTCTGTCGCCGAGGCTGGAGTGCA TTTTCCATTACTATTTTTTCTTTTTTTGAGA__GAGTCTCACTCTGTCGCCGAGGCTGGAGTGCA CTG C AL512343.2 Ensembl:ENSG00000272562 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1491249205 Functional Loss DEL dbSNP153 32..33 33 - - - 28044 RMVar_ID_28044 Human_SNP_ID_52013252 A-to-I Human chr1 - 226057610 226057610 226057610 AAATAAGCTGGGCATGATGGCGGTTGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAA AAATAAGCTGGGCATGATGGCGGTTGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAA T C AL512343.2 Ensembl:ENSG00000272562 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1383134558 Functional Loss SNV dbSNP153 33..33 33 - - - 28045 RMVar_ID_28045 Human_SNP_ID_52013328 A-to-I Human chr1 - 226057846 226057846 226057846 ACCAGTTCTGGCTAATTTTGTGTTATTAGTAGAGACCGGGTTTCTCCATGTTGGTCAGGCTGGCC ACCAGTTCTGGCTAATTTTGTGTTATTAGTAGTGACCGGGTTTCTCCATGTTGGTCAGGCTGGCC T A AL512343.2 Ensembl:ENSG00000272562 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1216424735 Functional Loss SNV dbSNP153 33..33 33 - - - 28046 RMVar_ID_28046 Human_SNP_ID_52013454 A-to-I Human chr1 - 226058299 226058299 226058299 AGGCATGGTCGTGGGCACTTGTAATCCCAGCTACTTGGGAGGCCTGAGGCAGGAGAATCACTTGA AGGCATGGTCGTGGGCACTTGTAATCCCAGCTGCTTGGGAGGCCTGAGGCAGGAGAATCACTTGA T C AL512343.2 Ensembl:ENSG00000272562 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054510630 Functional Loss SNV dbSNP153 33..33 33 - - - 28047 RMVar_ID_28047 Human_SNP_ID_52013455 A-to-I Human chr1 - 226058299 226058299 226058299 AGGCATGGTCGTGGGCACTTGTAATCCCAGCTACTTGGGAGGCCTGAGGCAGGAGAATCACTTGA AGGCATGGTCGTGGGCACTTGTAATCCCAGCTCCTTGGGAGGCCTGAGGCAGGAGAATCACTTGA T G AL512343.2 Ensembl:ENSG00000272562 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054510630 Functional Loss SNV dbSNP153 33..33 33 - - - 28048 RMVar_ID_28048 Human_SNP_ID_52013459 A-to-I Human chr1 - 226058309 226058309 226058309 AAAATTAGCCAGGCATGGTCGTGGGCACTTGTAATCCCAGCTACTTGGGAGGCCTGAGGCAGGAG AAAATTAGCCAGGCATGGTCGTGGGCACTTGTTATCCCAGCTACTTGGGAGGCCTGAGGCAGGAG T A AL512343.2 Ensembl:ENSG00000272562 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1333446083 Functional Loss SNV dbSNP153 33..33 33 - - - 28049 RMVar_ID_28049 Human_SNP_ID_52016341 A-to-I Human chr1 + 226067619 226067619 226067619 AAAAAATTAGCTTGGCGTGGTGGCAGGCGCCTATAATCCCAGCTACTAGGGAGGCTGAGGCAGGA AAAAAATTAGCTTGGCGTGGTGGCAGGCGCCTGTAATCCCAGCTACTAGGGAGGCTGAGGCAGGA A G H3-3A Ensembl:ENSG00000163041 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1305403185 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77982,RMVar_hsa_circ_140083 28050 RMVar_ID_28050 Human_SNP_ID_52016732 A-to-I Human chr1 + 226069110 226069110 226069110 ACTCTGTCACCTAGGCTGGAGTGCAGTGGTGCAATCTCGGCTTACTGCAGCCTCCGCCTCCCGGG ACTCTGTCACCTAGGCTGGAGTGCAGTGGTGCTATCTCGGCTTACTGCAGCCTCCGCCTCCCGGG A T H3-3A Ensembl:ENSG00000163041 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1220274490 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77982,RMVar_hsa_circ_140083 28051 RMVar_ID_28051 Human_SNP_ID_52016795 A-to-I Human chr1 + 226069261 226069261 226069261 TAGAGACAAGGTTTCTCCGTGTTGGTCAGTCTAGTCTCAAGCTCCTGACCTCGGGTGATCTGCCT TAGAGACAAGGTTTCTCCGTGTTGGTCAGTCTCGTCTCAAGCTCCTGACCTCGGGTGATCTGCCT A C H3-3A Ensembl:ENSG00000163041 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs550928131 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77982,RMVar_hsa_circ_140083 28052 RMVar_ID_28052 Human_SNP_ID_52016908 A-to-I Human chr1 + 226069670 226069670 226069670 CCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAATTAGCTGGACGTGATGGTGCA CCTGGCCAACATGGTGAAACCCCATCTCTACTGAAAATACAAAATTAGCTGGACGTGATGGTGCA A G H3-3A Ensembl:ENSG00000163041 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs111242638 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77982,RMVar_hsa_circ_140083 28053 RMVar_ID_28053 Human_SNP_ID_52016924 A-to-I Human chr1 + 226069716 226069716 226069716 AGCTGGACGTGATGGTGCATGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCC AGCTGGACGTGATGGTGCATGCCTGTAATCCCTGCTACTCGGGAGGCTGAGGCAGGAGAATTGCC A T H3-3A Ensembl:ENSG00000163041 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs763534050 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77982,RMVar_hsa_circ_140083 28054 RMVar_ID_28054 Human_SNP_ID_52020529 A-to-I Human chr1 + 226081660 226081660 226081660 GCCTGTAATCCCAGCACTGTGGAGGGCGAAGCAGGCGGATTGCTTGAGCCCAGGAGTTCCAGAAC GCCTGTAATCCCAGCACTGTGGAGGGCGAAGCCGGCGGATTGCTTGAGCCCAGGAGTTCCAGAAC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs555159760 Functional Loss SNV dbSNP153 33..33 33 - - - 28055 RMVar_ID_28055 Human_SNP_ID_52035449 A-to-I Human chr1 - 226140284 226140284 226140284 CCATGCCGGGCTAATTTTTTGTATTTTTTAGTAGAGACGAGGTTTCACCATGTTGGCCAGGCTGG CCATGCCGGGCTAATTTTTTGTATTTTTTAGTGGAGACGAGGTTTCACCATGTTGGCCAGGCTGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1317653238 Functional Loss SNV dbSNP153 33..33 33 - - - 28056 RMVar_ID_28056 Human_SNP_ID_52035534 A-to-I Human chr1 - 226140542 226140542 226140542 CCACACTTTGGGTTTTTGGTCTCGAACTCCTGACCTCAAGTGATCTGCCCGCTTCAGCCTCCCAA CCACACTTTGGGTTTTTGGTCTCGAACTCCTGGCCTCAAGTGATCTGCCCGCTTCAGCCTCCCAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1045694423 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10810681 28057 RMVar_ID_28057 Human_SNP_ID_52035799 A-to-I Human chr1 - 226141617 226141617 226141617 GGGAGGCTGAGGCACAAGAATCGCTTGAACTCAGGAGGCGGATGTTGCAGTGAGATGAGATCGTG GGGAGGCTGAGGCACAAGAATCGCTTGAACTCGGGAGGCGGATGTTGCAGTGAGATGAGATCGTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs990120738 Functional Loss SNV dbSNP153 33..33 33 - - - 28058 RMVar_ID_28058 Human_SNP_ID_52035912 A-to-I Human chr1 - 226142064 226142064 226142064 CGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCACCCGGCCCGGAGAA CGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTGCAGGCGTGAGCCACTGCACCCGGCCCGGAGAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1425463619 Functional Loss SNV dbSNP153 33..33 33 - - - 28059 RMVar_ID_28059 Human_SNP_ID_52043670 A-to-I Human chr1 - 226171726 226171726 226171726 CCAGCCTGGCCAACCCAACATGGTGAAACCCCATCTCTGTGAAAAATACAAAAATTAGCCAGGCA CCAGCCTGGCCAACCCAACATGGTGAAACCCCGTCTCTGTGAAAAATACAAAAATTAGCCAGGCA T C ACBD3 Ensembl:ENSG00000182827 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1457545884 Functional Loss SNV dbSNP153 33..33 33 - - - 28060 RMVar_ID_28060 Human_SNP_ID_52044003 A-to-I Human chr1 - 226172904 226172904 226172904 TCACCCAGGCTGGAGTTCGGTGGTGCTTTCACAGTCTATTGGAGCCTCGACCTTCAGGCTCAAGC TCACCCAGGCTGGAGTTCGGTGGTGCTTTCACGGTCTATTGGAGCCTCGACCTTCAGGCTCAAGC T C ACBD3 Ensembl:ENSG00000182827 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1398871242 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17556797 28061 RMVar_ID_28061 Human_SNP_ID_52045550 A-to-I Human chr1 - 226178386 226178386 226178386 TTTTGTACTTTTAGTAGAGACGGGGTTTTACCATGTTAGCCAGGATGGTCTCGAACTCCTGACCT TTTTGTACTTTTAGTAGAGACGGGGTTTTACCGTGTTAGCCAGGATGGTCTCGAACTCCTGACCT T C ACBD3 Ensembl:ENSG00000182827 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1337748142 Functional Loss SNV dbSNP153 33..33 33 - - - 28062 RMVar_ID_28062 Human_SNP_ID_52061758 A-to-I Human chr1 - 226244026 226244026 226244026 AGTAAAAATACAAAACTTAGCCCGGCGCAGGTAGCCTGCACCTGTAATCCCAGCTATTCGGGAGG AGTAAAAATACAAAACTTAGCCCGGCGCAGGTGGCCTGCACCTGTAATCCCAGCTATTCGGGAGG T C LIN9 Ensembl:ENSG00000183814 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs571495540 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54467,RMVar_hsa_circ_71420,RMVar_hsa_circ_140090,RMVar_hsa_circ_113761,RMVar_hsa_circ_372244,RMVar_hsa_circ_71487,RMVar_hsa_circ_362820,RMVar_hsa_circ_140091,RMVar_hsa_circ_346177,RMVar_hsa_circ_140092,RMVar_hsa_circ_140093 28063 RMVar_ID_28063 Human_SNP_ID_52071111 A-to-I Human chr1 - 226283048 226283048 226283048 ACAAGACCAAGGTGGGAGGATCACTTGAACCCAGGACTTGAGACTGCAGTGAGCTGTGATTGCCC ACAAGACCAAGGTGGGAGGATCACTTGAACCCGGGACTTGAGACTGCAGTGAGCTGTGATTGCCC T C LIN9 Ensembl:ENSG00000183814 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1431133147 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5769382,Human_RBP_ID_8300491,Human_RBP_ID_10812553 RMVar_hsa_circ_1289,RMVar_hsa_circ_54467,RMVar_hsa_circ_76917,RMVar_hsa_circ_362820,RMVar_hsa_circ_140093,RMVar_hsa_circ_310195,RMVar_hsa_circ_31564,RMVar_hsa_circ_140095,RMVar_hsa_circ_311010,RMVar_hsa_circ_140094,RMVar_hsa_circ_270180,RMVar_hsa_circ_140096,RMVar_hsa_circ_95872,RMVar_hsa_circ_294413,RMVar_hsa_circ_268424,RMVar_hsa_circ_140099,RMVar_hsa_circ_140100,RMVar_hsa_circ_51172,RMVar_hsa_circ_285975 28064 RMVar_ID_28064 Human_SNP_ID_52075274 A-to-I Human chr1 - 226300079 226300079 226300079 ACAAAATTATCCGGGAGTGGTGGCAGGTGCCTATAATCCCAGCTACTTGAGAGGCTGAGGCAGGA ACAAAATTATCCGGGAGTGGTGGCAGGTGCCTGTAATCCCAGCTACTTGAGAGGCTGAGGCAGGA T C LIN9 Ensembl:ENSG00000183814 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1288149137 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76917,RMVar_hsa_circ_140095,RMVar_hsa_circ_311010,RMVar_hsa_circ_95872,RMVar_hsa_circ_140099,RMVar_hsa_circ_11026,RMVar_hsa_circ_140101,RMVar_hsa_circ_311447 28065 RMVar_ID_28065 Human_SNP_ID_52148267 A-to-I Human chr1 + 226604201 226604201 226604201 ATTTTCCCCGCTTGGGCTGGGGGCGGCTGCTGAGGGGGTGAAGAAGAGATAGCAATTTATGTCGC ATTTTCCCCGCTTGGGCTGGGGGCGGCTGCTGCGGGGGTGAAGAAGAGATAGCAATTTATGTCGC A C STUM Ensembl:ENSG00000203685 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs891499654 Functional Loss SNV dbSNP153 33..33 33 - - - 28066 RMVar_ID_28066 Human_SNP_ID_52218101 A-to-I Human chr1 + 226888148 226888148 226888148 CTTCACTGATGCTGCTGTTCCTCTTCACCTATATCTACCTTGGGTAAGTGACAGATAAGCAGCAG CTTCACTGATGCTGCTGTTCCTCTTCACCTATGTCTACCTTGGGTAAGTGACAGATAAGCAGCAG A G PSEN2 Ensembl:ENSG00000143801 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1401090704 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17741135 Human_Splice_Rec_193424,Human_Splice_Rec_193425,Human_Splice_Rec_193448,Human_Splice_Rec_193449,Human_Splice_Rec_193466,Human_Splice_Rec_193467,Human_Splice_Rec_193484,Human_Splice_Rec_193485,Human_Splice_Rec_193504,Human_Splice_Rec_193505,Human_Splice_Rec_193520,Human_Splice_Rec_193521 RMVar_hsa_circ_5885,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_127596,RMVar_hsa_circ_140115,RMVar_hsa_circ_284714,RMVar_hsa_circ_107246,RMVar_hsa_circ_117527,RMVar_hsa_circ_140116,RMVar_hsa_circ_140117,RMVar_hsa_circ_140118,RMVar_hsa_circ_272297,RMVar_hsa_circ_140120,RMVar_hsa_circ_140121 28067 RMVar_ID_28067 Human_SNP_ID_52228634 A-to-I Human chr1 + 226932770 226932770 226932770 AAAAAAATTAAAATAAAATAGTCGAGTATGGTAGTGCTTGCCTGTAGTCCCAGCTATTCAGGAGG AAAAAAATTAAAATAAAATAGTCGAGTATGGTGGTGCTTGCCTGTAGTCCCAGCTATTCAGGAGG A G COQ8A Ensembl:ENSG00000163050 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs774019153 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22236,RMVar_hsa_circ_99597,RMVar_hsa_circ_140122,RMVar_hsa_circ_140123 28068 RMVar_ID_28068 Human_SNP_ID_52251681 A-to-I Human chr1 - 227015048 227015048 227015048 GGGAGGCTAAGGTGGGAGGGTTACTTGAGCCCAGGAGTTTGAGGCTGCGGGGAGCTATGATTGCC GGGAGGCTAAGGTGGGAGGGTTACTTGAGCCCGGGAGTTTGAGGCTGCGGGGAGCTATGATTGCC T C CDC42BPA Ensembl:ENSG00000143776 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,cerebellum - 29129909,30559470 RNA-Seq:(High) rs984176671 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24649147 RMVar_hsa_circ_140132,RMVar_hsa_circ_122149,RMVar_hsa_circ_140127,RMVar_hsa_circ_78754,RMVar_hsa_circ_267374,RMVar_hsa_circ_140126,RMVar_hsa_circ_331541,RMVar_hsa_circ_375412,RMVar_hsa_circ_140129,RMVar_hsa_circ_279905,RMVar_hsa_circ_140130,RMVar_hsa_circ_299315,RMVar_hsa_circ_299714,RMVar_hsa_circ_343223,RMVar_hsa_circ_281936,RMVar_hsa_circ_15430,RMVar_hsa_circ_116457,RMVar_hsa_circ_140134,RMVar_hsa_circ_140135,RMVar_hsa_circ_140133 28069 RMVar_ID_28069 Human_SNP_ID_52251684 A-to-I Human chr1 - 227015071 227015071 227015071 TGTGCCTGTAGTCCTGGTTACTCGGGAGGCTAAGGTGGGAGGGTTACTTGAGCCCAGGAGTTTGA TGTGCCTGTAGTCCTGGTTACTCGGGAGGCTAGGGTGGGAGGGTTACTTGAGCCCAGGAGTTTGA T C CDC42BPA Ensembl:ENSG00000143776 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1002904635 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_140132,RMVar_hsa_circ_122149,RMVar_hsa_circ_140127,RMVar_hsa_circ_78754,RMVar_hsa_circ_267374,RMVar_hsa_circ_140126,RMVar_hsa_circ_331541,RMVar_hsa_circ_375412,RMVar_hsa_circ_140129,RMVar_hsa_circ_279905,RMVar_hsa_circ_140130,RMVar_hsa_circ_299315,RMVar_hsa_circ_299714,RMVar_hsa_circ_343223,RMVar_hsa_circ_281936,RMVar_hsa_circ_15430,RMVar_hsa_circ_116457,RMVar_hsa_circ_140134,RMVar_hsa_circ_140135,RMVar_hsa_circ_140133 28070 RMVar_ID_28070 Human_SNP_ID_52254558 A-to-I Human chr1 - 227026913 227026913 227026913 AGTGGTTGCATGCCTGTTGTCCCAACTACCCAAGAGGCTGAGGTAGGAGGATCACTTGAGCTATG AGTGGTTGCATGCCTGTTGTCCCAACTACCCAGGAGGCTGAGGTAGGAGGATCACTTGAGCTATG T C CDC42BPA Ensembl:ENSG00000143776 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1330096090 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557439 RMVar_hsa_circ_140127,RMVar_hsa_circ_78754,RMVar_hsa_circ_267374,RMVar_hsa_circ_140126,RMVar_hsa_circ_375412,RMVar_hsa_circ_140129,RMVar_hsa_circ_279905,RMVar_hsa_circ_281936,RMVar_hsa_circ_15430,RMVar_hsa_circ_116457,RMVar_hsa_circ_140134,RMVar_hsa_circ_140135,RMVar_hsa_circ_140133,RMVar_hsa_circ_18464,RMVar_hsa_circ_16441,RMVar_hsa_circ_324571,RMVar_hsa_circ_347050,RMVar_hsa_circ_320182,RMVar_hsa_circ_294952,RMVar_hsa_circ_314708,RMVar_hsa_circ_293389,RMVar_hsa_circ_140138,RMVar_hsa_circ_140140,RMVar_hsa_circ_140141,RMVar_hsa_circ_140139,RMVar_hsa_circ_299199,RMVar_hsa_circ_140137,RMVar_hsa_circ_366440,RMVar_hsa_circ_351419,RMVar_hsa_circ_286726,RMVar_hsa_circ_265613,RMVar_hsa_circ_284780,RMVar_hsa_circ_140145,RMVar_hsa_circ_140146,RMVar_hsa_circ_140144,RMVar_hsa_circ_307363,RMVar_hsa_circ_312160,RMVar_hsa_circ_52461,RMVar_hsa_circ_56068,RMVar_hsa_circ_140147,RMVar_hsa_circ_140148 28071 RMVar_ID_28071 Human_SNP_ID_52254561 A-to-I Human chr1 - 227026921 227026921 227026921 CCAGGTGTAGTGGTTGCATGCCTGTTGTCCCAACTACCCAAGAGGCTGAGGTAGGAGGATCACTT CCAGGTGTAGTGGTTGCATGCCTGTTGTCCCAGCTACCCAAGAGGCTGAGGTAGGAGGATCACTT T C CDC42BPA Ensembl:ENSG00000143776 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924766461 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557439 RMVar_hsa_circ_140127,RMVar_hsa_circ_78754,RMVar_hsa_circ_267374,RMVar_hsa_circ_140126,RMVar_hsa_circ_375412,RMVar_hsa_circ_140129,RMVar_hsa_circ_279905,RMVar_hsa_circ_281936,RMVar_hsa_circ_15430,RMVar_hsa_circ_116457,RMVar_hsa_circ_140134,RMVar_hsa_circ_140135,RMVar_hsa_circ_140133,RMVar_hsa_circ_18464,RMVar_hsa_circ_16441,RMVar_hsa_circ_324571,RMVar_hsa_circ_347050,RMVar_hsa_circ_320182,RMVar_hsa_circ_294952,RMVar_hsa_circ_314708,RMVar_hsa_circ_293389,RMVar_hsa_circ_140138,RMVar_hsa_circ_140140,RMVar_hsa_circ_140141,RMVar_hsa_circ_140139,RMVar_hsa_circ_299199,RMVar_hsa_circ_140137,RMVar_hsa_circ_366440,RMVar_hsa_circ_351419,RMVar_hsa_circ_286726,RMVar_hsa_circ_265613,RMVar_hsa_circ_284780,RMVar_hsa_circ_140145,RMVar_hsa_circ_140146,RMVar_hsa_circ_140144,RMVar_hsa_circ_307363,RMVar_hsa_circ_312160,RMVar_hsa_circ_52461,RMVar_hsa_circ_56068,RMVar_hsa_circ_140147,RMVar_hsa_circ_140148 28072 RMVar_ID_28072 Human_SNP_ID_52264917 A-to-I Human chr1 - 227069076 227069076 227069076 TAGTGACCAAAATAGACAAAGTCCTTCCCACTAGAACTTACATTCCAGTGGGAAGAATTAGAAGC TAGTGACCAAAATAGACAAAGTCCTTCCCACTGGAACTTACATTCCAGTGGGAAGAATTAGAAGC T C CDC42BPA Ensembl:ENSG00000143776 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs902466613 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_140127,RMVar_hsa_circ_16441,RMVar_hsa_circ_347050,RMVar_hsa_circ_320182,RMVar_hsa_circ_265613,RMVar_hsa_circ_331557,RMVar_hsa_circ_140149,RMVar_hsa_circ_54494,RMVar_hsa_circ_66125,RMVar_hsa_circ_21458,RMVar_hsa_circ_737,RMVar_hsa_circ_17182,RMVar_hsa_circ_140154,RMVar_hsa_circ_85232,RMVar_hsa_circ_73106,RMVar_hsa_circ_333420,RMVar_hsa_circ_103805,RMVar_hsa_circ_140155,RMVar_hsa_circ_32315,RMVar_hsa_circ_288433,RMVar_hsa_circ_140153,RMVar_hsa_circ_283424,RMVar_hsa_circ_19872,RMVar_hsa_circ_75158,RMVar_hsa_circ_140158,RMVar_hsa_circ_345011,RMVar_hsa_circ_27826,RMVar_hsa_circ_71962,RMVar_hsa_circ_3240,RMVar_hsa_circ_140163,RMVar_hsa_circ_118595,RMVar_hsa_circ_102704,RMVar_hsa_circ_140162 28073 RMVar_ID_28073 Human_SNP_ID_52292568 A-to-I Human chr1 - 227178598 227178598 227178598 GTAGCTACCCAGGAGGCTGAGTCAGGAGAATCACTTGAATCCGGGAGGTAGAGGTTGTGGTGAGC GTAGCTACCCAGGAGGCTGAGTCAGGAGAATCCCTTGAATCCGGGAGGTAGAGGTTGTGGTGAGC T G CDC42BPA Ensembl:ENSG00000143776 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1339678880 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19872,RMVar_hsa_circ_309958,RMVar_hsa_circ_361451,RMVar_hsa_circ_64114,RMVar_hsa_circ_72536,RMVar_hsa_circ_327294,RMVar_hsa_circ_322965,RMVar_hsa_circ_7627,RMVar_hsa_circ_140175,RMVar_hsa_circ_19132,RMVar_hsa_circ_315276,RMVar_hsa_circ_140183,RMVar_hsa_circ_319514,RMVar_hsa_circ_357960,RMVar_hsa_circ_363161,RMVar_hsa_circ_325902,RMVar_hsa_circ_140184,RMVar_hsa_circ_140187,RMVar_hsa_circ_45124,RMVar_hsa_circ_95309,RMVar_hsa_circ_291766,RMVar_hsa_circ_140186,RMVar_hsa_circ_284598,RMVar_hsa_circ_140189,RMVar_hsa_circ_140190,RMVar_hsa_circ_140188 28074 RMVar_ID_28074 Human_SNP_ID_52297875 A-to-I Human chr1 - 227198886 227198883 227198886 AAAATTAGCCGGGCGTGGTGGTGGGCACCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTAGCCGGGCGTGGTGGTGGGCACCTGT___CCCAGCTACTCGGGAGGCTGAGGCAGGAGA GACT G CDC42BPA Ensembl:ENSG00000143776 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1435819833 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_19872,RMVar_hsa_circ_309958,RMVar_hsa_circ_361451,RMVar_hsa_circ_64114,RMVar_hsa_circ_72536,RMVar_hsa_circ_327294,RMVar_hsa_circ_322965,RMVar_hsa_circ_7627,RMVar_hsa_circ_140175,RMVar_hsa_circ_19132,RMVar_hsa_circ_315276,RMVar_hsa_circ_140183,RMVar_hsa_circ_319514,RMVar_hsa_circ_357960,RMVar_hsa_circ_325902,RMVar_hsa_circ_140184,RMVar_hsa_circ_140187,RMVar_hsa_circ_45124,RMVar_hsa_circ_95309,RMVar_hsa_circ_291766,RMVar_hsa_circ_140186,RMVar_hsa_circ_284598,RMVar_hsa_circ_140189,RMVar_hsa_circ_140190,RMVar_hsa_circ_140188,RMVar_hsa_circ_140191,RMVar_hsa_circ_140193,RMVar_hsa_circ_140195,RMVar_hsa_circ_273569,RMVar_hsa_circ_281509,RMVar_hsa_circ_273179,RMVar_hsa_circ_140194,RMVar_hsa_circ_140192 28075 RMVar_ID_28075 Human_SNP_ID_52297876 A-to-I Human chr1 - 227198886 227198886 227198886 AAAATTAGCCGGGCGTGGTGGTGGGCACCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTAGCCGGGCGTGGTGGTGGGCACCTGTTGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA T A CDC42BPA Ensembl:ENSG00000143776 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs969198261 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19872,RMVar_hsa_circ_309958,RMVar_hsa_circ_361451,RMVar_hsa_circ_64114,RMVar_hsa_circ_72536,RMVar_hsa_circ_327294,RMVar_hsa_circ_322965,RMVar_hsa_circ_7627,RMVar_hsa_circ_140175,RMVar_hsa_circ_19132,RMVar_hsa_circ_315276,RMVar_hsa_circ_140183,RMVar_hsa_circ_319514,RMVar_hsa_circ_357960,RMVar_hsa_circ_325902,RMVar_hsa_circ_140184,RMVar_hsa_circ_140187,RMVar_hsa_circ_45124,RMVar_hsa_circ_95309,RMVar_hsa_circ_291766,RMVar_hsa_circ_140186,RMVar_hsa_circ_284598,RMVar_hsa_circ_140189,RMVar_hsa_circ_140190,RMVar_hsa_circ_140188,RMVar_hsa_circ_140191,RMVar_hsa_circ_140193,RMVar_hsa_circ_140195,RMVar_hsa_circ_273569,RMVar_hsa_circ_281509,RMVar_hsa_circ_273179,RMVar_hsa_circ_140194,RMVar_hsa_circ_140192 28076 RMVar_ID_28076 Human_SNP_ID_52314509 A-to-I Human chr1 - 227263644 227263644 227263644 CTGGGAGGCGGAGACTGCAGTGAGCCAAGATCATGCCATTACACTGCAGCCTGGGTGCAGAGCGA CTGGGAGGCGGAGACTGCAGTGAGCCAAGATCGTGCCATTACACTGCAGCCTGGGTGCAGAGCGA T C CDC42BPA Ensembl:ENSG00000143776 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1194823826 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_140199 28077 RMVar_ID_28077 Human_SNP_ID_52326152 A-to-I Human chr1 - 227308333 227308333 227308333 GCTAATTTTTTTCTTGTATTTTAGTAGACACAAGGTTTCACCATGTTGCCCAGGTTCATCTTGAA GCTAATTTTTTTCTTGTATTTTAGTAGACACAGGGTTTCACCATGTTGCCCAGGTTCATCTTGAA T C CDC42BPA Ensembl:ENSG00000143776 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928481095 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_140199 28078 RMVar_ID_28078 Human_SNP_ID_52326849 A-to-I Human chr1 - 227310851 227310851 227310851 GCGTCTCTACTAAAAATTCAAAAAAAAAAATTAGCCGGGCGCGGTGACGGGTGCCTGTAGTCCCA GCGTCTCTACTAAAAATTCAAAAAAAAAAATTCGCCGGGCGCGGTGACGGGTGCCTGTAGTCCCA T G CDC42BPA Ensembl:ENSG00000143776 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1228321165 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_99823 RMVar_hsa_circ_140199 28079 RMVar_ID_28079 Human_SNP_ID_52326989 A-to-I Human chr1 - 227311299 227311299 227311299 ATAATTGTTATGAGAGACCATCATGGCTCACTACAGCCTCAACCTCCTGGGCTCAGGATCCTCCT ATAATTGTTATGAGAGACCATCATGGCTCACTGCAGCCTCAACCTCCTGGGCTCAGGATCCTCCT T C CDC42BPA Ensembl:ENSG00000143776 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1443904024 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_140199 28080 RMVar_ID_28080 Human_SNP_ID_52351731 A-to-I Human chr1 - 227411175 227411175 227411175 TCATCATCTCCCCTAGAAGCTAAAAATAAGGCAATCTGGAAAGAATTCACAGGAAGATAGTGAGG TCATCATCTCCCCTAGAAGCTAAAAATAAGGCGATCTGGAAAGAATTCACAGGAAGATAGTGAGG T C NUCKS1P1 Ensembl:ENSG00000232864 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1438143150 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4090204,Human_RBP_ID_8241431,Human_RBP_ID_17456763,Human_RBP_ID_26390519 28081 RMVar_ID_28081 Human_SNP_ID_52440397 A-to-I Human chr1 + 227782133 227782133 227782133 CAGCCTCCCACAGTGCTGAGATTACAGGCGTGAGCCACTGCACCCAGCACTCTGATGTTATTTTT CAGCCTCCCACAGTGCTGAGATTACAGGCGTGGGCCACTGCACCCAGCACTCTGATGTTATTTTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1370664676 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5773037,Human_RBP_ID_10822300 28082 RMVar_ID_28082 Human_SNP_ID_52533346 A-to-I Human chr1 + 228146643 228146643 228146643 CCCAGCAGTCTCGTATCTCCATCAGTGAGGACAGTGTGAGAAATGGTGTCTGGCTCAGGCACTTG CCCAGCAGTCTCGTATCTCCATCAGTGAGGACGGTGTGAGAAATGGTGTCTGGCTCAGGCACTTG A G GUK1 Ensembl:ENSG00000143774 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1264661427 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10823691,Human_RBP_ID_17071674,Human_RBP_ID_18565456,Human_RBP_ID_27554992 RMVar_hsa_circ_3447,RMVar_hsa_circ_84116,RMVar_hsa_circ_140220 28083 RMVar_ID_28083 Human_SNP_ID_52542411 A-to-I Human chr1 - 228175930 228175930 228175930 ACAACTCCCAAAGCCCGAGCCCCAGCCTGCAGACCCTGGACACCACCCCGCTTCCAGGCACAGGG ACAACTCCCAAAGCCCGAGCCCCAGCCTGCAGGCCCTGGACACCACCCCGCTTCCAGGCACAGGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1021989018 Functional Loss SNV dbSNP153 33..33 33 - - - 28084 RMVar_ID_28084 Human_SNP_ID_52542858 A-to-I Human chr1 + 228177553 228177553 228177553 GCTCTGTTGGCCAGGCTGGAGCTCAGTGGCACAATCTCTGCTCACTGCAACCTCTGCCTCCCAGG GCTCTGTTGGCCAGGCTGGAGCTCAGTGGCACCATCTCTGCTCACTGCAACCTCTGCCTCCCAGG A C IBA57 Ensembl:ENSG00000181873 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1158499086 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10823962 28085 RMVar_ID_28085 Human_SNP_ID_52542873 A-to-I Human chr1 + 228177607 228177607 228177607 TGCCTCCCAGGTTCCAGTGATTTTCCTGCCTCAGCCTCCTGGGTAGCTGGGACTACAGGCACATG TGCCTCCCAGGTTCCAGTGATTTTCCTGCCTCGGCCTCCTGGGTAGCTGGGACTACAGGCACATG A G IBA57 Ensembl:ENSG00000181873 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1008122441 Functional Loss SNV dbSNP153 33..33 33 - - - 28086 RMVar_ID_28086 Human_SNP_ID_52543060 A-to-I Human chr1 + 228178434 228178434 228178434 TCAAGACTCTGTCTCTTAAAAAAAAAAAAATTAGCCAGGCATGGTGGTCCACACCTGTGGTCCCA TCAAGACTCTGTCTCTTAAAAAAAAAAAAATTTGCCAGGCATGGTGGTCCACACCTGTGGTCCCA A T IBA57 Ensembl:ENSG00000181873 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1036825012 Functional Loss SNV dbSNP153 33..33 33 - - - 28087 RMVar_ID_28087 Human_SNP_ID_52543659 A-to-I Human chr1 + 228180746 228180746 228180746 ACAGCTCACTACAGCCTCAACCTTCTGGGCTCAGATGATTCTCCTGCCTCAGCCTCCTGAGTAGC ACAGCTCACTACAGCCTCAACCTTCTGGGCTCCGATGATTCTCCTGCCTCAGCCTCCTGAGTAGC A C IBA57 Ensembl:ENSG00000181873 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1411542093 Functional Loss SNV dbSNP153 33..33 33 - - - 28088 RMVar_ID_28088 Human_SNP_ID_52543660 A-to-I Human chr1 + 228180748 228180748 228180748 AGCTCACTACAGCCTCAACCTTCTGGGCTCAGATGATTCTCCTGCCTCAGCCTCCTGAGTAGCAG AGCTCACTACAGCCTCAACCTTCTGGGCTCAGGTGATTCTCCTGCCTCAGCCTCCTGAGTAGCAG A G IBA57 Ensembl:ENSG00000181873 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1030175084 Functional Loss SNV dbSNP153 33..33 33 - - - 28089 RMVar_ID_28089 Human_SNP_ID_52543668 A-to-I Human chr1 + 228180788 228180788 228180788 CCTGCCTCAGCCTCCTGAGTAGCAGGAACTACAGGTGTGAGTCATCACACTCAGCTAATTTTTTT CCTGCCTCAGCCTCCTGAGTAGCAGGAACTACCGGTGTGAGTCATCACACTCAGCTAATTTTTTT A C IBA57 Ensembl:ENSG00000181873 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1320218035 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5773713 28090 RMVar_ID_28090 Human_SNP_ID_52543700 A-to-I Human chr1 + 228180911 228180911 228180911 GAATTTCTGGGCTCAGGTGATCTTCCCACCTCAGCCTCCTGAGTAGCTGGGACCACAGGTGCATG GAATTTCTGGGCTCAGGTGATCTTCCCACCTCCGCCTCCTGAGTAGCTGGGACCACAGGTGCATG A C IBA57 Ensembl:ENSG00000181873 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1295047892 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1393865 28091 RMVar_ID_28091 Human_SNP_ID_52565541 A-to-I Human chr1 + 228265927 228265927 228265927 AAAAAACAATTAAAAAATTAGCTGGGTGTTGTAGTGGGTGCCTGTAAGTCCTAGCTACTTGGGAG AAAAAACAATTAAAAAATTAGCTGGGTGTTGTTGTGGGTGCCTGTAAGTCCTAGCTACTTGGGAG A T OBSCN Ensembl:ENSG00000154358 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs543206794 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_363380,RMVar_hsa_circ_31451,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_140226,RMVar_hsa_circ_140227 28092 RMVar_ID_28092 Human_SNP_ID_52565798 A-to-I Human chr1 + 228267059 228267059 228267059 CTCCTGACTTGATGAGAATACAGGCGTGCACCACCATGCCTAGCTAATTTTTTAAGGAATTTTTT CTCCTGACTTGATGAGAATACAGGCGTGCACCGCCATGCCTAGCTAATTTTTTAAGGAATTTTTT A G OBSCN Ensembl:ENSG00000154358 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1333747568 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_363380,RMVar_hsa_circ_31451,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_140226,RMVar_hsa_circ_140227 28093 RMVar_ID_28093 Human_SNP_ID_52594197 A-to-I Human chr1 + 228358671 228358671 228358671 GTTGTGTGTTACTCAGCACGTTCTGCTTCCCTACGTGTTAACTCAGTTTGCTCTCAGTGCTCAGC GTTGTGTGTTACTCAGCACGTTCTGCTTCCCTGCGTGTTAACTCAGTTTGCTCTCAGTGCTCAGC A G OBSCN Ensembl:ENSG00000154358 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978653587 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267772,RMVar_hsa_circ_324283 28094 RMVar_ID_28094 Human_SNP_ID_52610683 A-to-I Human chr1 + 228412719 228412719 228412719 TTGAGTCCAGGAATTTGAGGCTGCAGTGAGCTATGATTGCATCACTGTGCTCCAGCCTGGGCCAC TTGAGTCCAGGAATTTGAGGCTGCAGTGAGCTCTGATTGCATCACTGTGCTCCAGCCTGGGCCAC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984631511 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24650696 28095 RMVar_ID_28095 Human_SNP_ID_52610684 A-to-I Human chr1 + 228412719 228412719 228412719 TTGAGTCCAGGAATTTGAGGCTGCAGTGAGCTATGATTGCATCACTGTGCTCCAGCCTGGGCCAC TTGAGTCCAGGAATTTGAGGCTGCAGTGAGCTGTGATTGCATCACTGTGCTCCAGCCTGGGCCAC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984631511 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24650696 28096 RMVar_ID_28096 Human_SNP_ID_52630136 A-to-I Human chr1 - 228486353 228486353 228486353 GGCGCCTGCCACGACGCCCGGCTAATTTTTGTATTTTTAGTACAGACGGGGTTTCACCATGTTGG GGCGCCTGCCACGACGCCCGGCTAATTTTTGTGTTTTTAGTACAGACGGGGTTTCACCATGTTGG T C AL139288.2 Ensembl:ENSG00000279306 Other exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1194030008 Functional Loss SNV dbSNP153 33..33 33 - - - 28097 RMVar_ID_28097 Human_SNP_ID_52631651 A-to-I Human chr1 + 228491208 228491208 228491208 GGCTAGGAGTTCGAGACCAGCCTGGGTAACATAGTGAGACCACCATCTGTACAAAAATTAATAAA GGCTAGGAGTTCGAGACCAGCCTGGGTAACATGGTGAGACCACCATCTGTACAAAAATTAATAAA A G RNF187 Ensembl:ENSG00000168159 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1236737486 Functional Loss SNV dbSNP153 33..33 33 - - - 28098 RMVar_ID_28098 Human_SNP_ID_52801885 A-to-I Human chr1 - 229264408 229264408 229264408 GGCCAGAAGACTCAGCAAGTCTGCTTTATTCTAGCCGCTCTGGTAGCCGATTAGATGGGGCCCAC GGCCAGAAGACTCAGCAAGTCTGCTTTATTCTGGCCGCTCTGGTAGCCGATTAGATGGGGCCCAC T C AL162595.1 Ensembl:ENSG00000177788 lincRNA intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1400832139 Functional Loss SNV dbSNP153 33..33 33 - - - 28099 RMVar_ID_28099 Human_SNP_ID_52802037 A-to-I Human chr1 - 229264986 229264983 229264986 AGGCATGGTGGCGCGCACATGTAGTCTCATCTACTCAGGAGGCCGAGGCAGGAGAATCGCTGGAA AGGCATGGTGGCGCGCACATGTAGTCTCATCT___CAGGAGGCCGAGGCAGGAGAATCGCTGGAA GAGT G AL162595.1 Ensembl:ENSG00000177788 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1242045954 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_8242032 28100 RMVar_ID_28100 Human_SNP_ID_52802703 A-to-I Human chr1 - 229267893 229267893 229267893 AGATGTAGTCTTGCTTTGTTGCACAGGCTGGAATGCAGTGGCGTGATCTCAGCTCACTATGACCT AGATGTAGTCTTGCTTTGTTGCACAGGCTGGAGTGCAGTGGCGTGATCTCAGCTCACTATGACCT T C AL162595.1 Ensembl:ENSG00000177788 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1294504703 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3335150 28101 RMVar_ID_28101 Human_SNP_ID_52802707 A-to-I Human chr1 - 229267925 229267925 229267925 ATACGTATGTATTTATTTTATTTTATTTTTTGAGATGTAGTCTTGCTTTGTTGCACAGGCTGGAA ATACGTATGTATTTATTTTATTTTATTTTTTGTGATGTAGTCTTGCTTTGTTGCACAGGCTGGAA T A AL162595.1 Ensembl:ENSG00000177788 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1367237486 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5774461 28102 RMVar_ID_28102 Human_SNP_ID_52804077 A-to-I Human chr1 + 229273484 229273484 229273484 AAATGAGGCCAGAGGTGATGGCTCACGCCTGTAATCCCAGCACTTTGGAAGGCCGAGTTGGGCGG AAATGAGGCCAGAGGTGATGGCTCACGCCTGTGATCCCAGCACTTTGGAAGGCCGAGTTGGGCGG A G RAB4A Ensembl:ENSG00000168118 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1245568498 Functional Loss SNV dbSNP153 33..33 33 - - - 28103 RMVar_ID_28103 Human_SNP_ID_52809212 A-to-I Human chr1 + 229295060 229295060 229295060 TCGCTCACCGTCACCTCAAATTCCTGGGATCAAACAGTCCTTCTGTCTCAGCCTCCTGAGTAGCT TCGCTCACCGTCACCTCAAATTCCTGGGATCAGACAGTCCTTCTGTCTCAGCCTCCTGAGTAGCT A G RAB4A Ensembl:ENSG00000168118 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1316398756 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_140254,RMVar_hsa_circ_358081,RMVar_hsa_circ_140255,RMVar_hsa_circ_140256 28104 RMVar_ID_28104 Human_SNP_ID_52850349 A-to-I Human chr1 - 229451155 229451155 229451155 TTCTCAAGGAATCTGCCTGCCTCGGCCTCCCAAAGAGCTGGGATTATAGACATGAGCCACTGTGC TTCTCAAGGAATCTGCCTGCCTCGGCCTCCCAGAGAGCTGGGATTATAGACATGAGCCACTGTGC T C NUP133 Ensembl:ENSG00000069248 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1394212220 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4030834,Human_RBP_ID_17557441 RMVar_hsa_circ_21411,RMVar_hsa_circ_81578,RMVar_hsa_circ_91523,RMVar_hsa_circ_95693,RMVar_hsa_circ_24928,RMVar_hsa_circ_323393,RMVar_hsa_circ_140259,RMVar_hsa_circ_140260,RMVar_hsa_circ_140261,RMVar_hsa_circ_345106,RMVar_hsa_circ_328469,RMVar_hsa_circ_306068,RMVar_hsa_circ_48105,RMVar_hsa_circ_140268,RMVar_hsa_circ_140265,RMVar_hsa_circ_140266,RMVar_hsa_circ_363633,RMVar_hsa_circ_291230,RMVar_hsa_circ_118325,RMVar_hsa_circ_140267,RMVar_hsa_circ_306351,RMVar_hsa_circ_73674,RMVar_hsa_circ_140269,RMVar_hsa_circ_140270 28105 RMVar_ID_28105 Human_SNP_ID_52853242 A-to-I Human chr1 - 229463367 229463367 229463367 TATGTCGCGTTTCTTTGTAAATTTTGTCCAGTAGCGAGATCACAGTTCACGACAGCCTCAACCTC TATGTCGCGTTTCTTTGTAAATTTTGTCCAGTTGCGAGATCACAGTTCACGACAGCCTCAACCTC T A NUP133 Ensembl:ENSG00000069248 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947898295 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_345164 RMVar_hsa_circ_35089,RMVar_hsa_circ_81578,RMVar_hsa_circ_91523,RMVar_hsa_circ_95693,RMVar_hsa_circ_24928,RMVar_hsa_circ_323393,RMVar_hsa_circ_140259,RMVar_hsa_circ_140260,RMVar_hsa_circ_140261,RMVar_hsa_circ_306068,RMVar_hsa_circ_48105,RMVar_hsa_circ_140268,RMVar_hsa_circ_140266,RMVar_hsa_circ_291230,RMVar_hsa_circ_118325,RMVar_hsa_circ_306351,RMVar_hsa_circ_73674,RMVar_hsa_circ_140269,RMVar_hsa_circ_140270,RMVar_hsa_circ_325677,RMVar_hsa_circ_54080,RMVar_hsa_circ_110361,RMVar_hsa_circ_292340,RMVar_hsa_circ_367218,RMVar_hsa_circ_140272,RMVar_hsa_circ_331935,RMVar_hsa_circ_297026,RMVar_hsa_circ_280823,RMVar_hsa_circ_44670,RMVar_hsa_circ_66606,RMVar_hsa_circ_39969,RMVar_hsa_circ_26722,RMVar_hsa_circ_140273,RMVar_hsa_circ_140275,RMVar_hsa_circ_140277,RMVar_hsa_circ_140276,RMVar_hsa_circ_140274,RMVar_hsa_circ_285651,RMVar_hsa_circ_294555,RMVar_hsa_circ_362050,RMVar_hsa_circ_298679,RMVar_hsa_circ_292588,RMVar_hsa_circ_36094,RMVar_hsa_circ_140280,RMVar_hsa_circ_140281,RMVar_hsa_circ_140282 28106 RMVar_ID_28106 Human_SNP_ID_52853603 A-to-I Human chr1 - 229464696 229464696 229464696 ATGTTTCTCAGCTTAAGTCTGTGGATAAATCCAGTAATCGGGAAAGATATGACAATCTGGAGATG ATGTTTCTCAGCTTAAGTCTGTGGATAAATCCGGTAATCGGGAAAGATATGACAATCTGGAGATG T C NUP133 Ensembl:ENSG00000069248 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs755831030 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_1739478,Human_RBP_ID_8744778,Human_RBP_ID_9268039,Human_RBP_ID_9359933,Human_RBP_ID_26856104,Human_RBP_ID_27589229 Human_Splice_Rec_197277 RMVar_hsa_circ_35089,RMVar_hsa_circ_81578,RMVar_hsa_circ_91523,RMVar_hsa_circ_95693,RMVar_hsa_circ_24928,RMVar_hsa_circ_323393,RMVar_hsa_circ_140259,RMVar_hsa_circ_140260,RMVar_hsa_circ_140261,RMVar_hsa_circ_306068,RMVar_hsa_circ_48105,RMVar_hsa_circ_140268,RMVar_hsa_circ_140266,RMVar_hsa_circ_291230,RMVar_hsa_circ_118325,RMVar_hsa_circ_306351,RMVar_hsa_circ_73674,RMVar_hsa_circ_140269,RMVar_hsa_circ_140270,RMVar_hsa_circ_325677,RMVar_hsa_circ_54080,RMVar_hsa_circ_110361,RMVar_hsa_circ_292340,RMVar_hsa_circ_367218,RMVar_hsa_circ_140272,RMVar_hsa_circ_331935,RMVar_hsa_circ_297026,RMVar_hsa_circ_44670,RMVar_hsa_circ_66606,RMVar_hsa_circ_39969,RMVar_hsa_circ_99295,RMVar_hsa_circ_26722,RMVar_hsa_circ_140273,RMVar_hsa_circ_140275,RMVar_hsa_circ_140276,RMVar_hsa_circ_140274,RMVar_hsa_circ_285651,RMVar_hsa_circ_362050,RMVar_hsa_circ_298679,RMVar_hsa_circ_292588,RMVar_hsa_circ_36094,RMVar_hsa_circ_352201,RMVar_hsa_circ_140281,RMVar_hsa_circ_140282,RMVar_hsa_circ_366436,RMVar_hsa_circ_376218,RMVar_hsa_circ_290344,RMVar_hsa_circ_316061,RMVar_hsa_circ_125731,RMVar_hsa_circ_103300,RMVar_hsa_circ_114214,RMVar_hsa_circ_100760,RMVar_hsa_circ_77689,RMVar_hsa_circ_140284,RMVar_hsa_circ_140288,RMVar_hsa_circ_140290,RMVar_hsa_circ_97505,RMVar_hsa_circ_140291,RMVar_hsa_circ_140289,RMVar_hsa_circ_140286,RMVar_hsa_circ_140287,RMVar_hsa_circ_140285,RMVar_hsa_circ_94892,RMVar_hsa_circ_140283,RMVar_hsa_circ_352806,RMVar_hsa_circ_374880,RMVar_hsa_circ_291264,RMVar_hsa_circ_91370,RMVar_hsa_circ_140295,RMVar_hsa_circ_140297,RMVar_hsa_circ_22321,RMVar_hsa_circ_140298,RMVar_hsa_circ_140296,RMVar_hsa_circ_140294 28107 RMVar_ID_28107 Human_SNP_ID_52859902 A-to-I Human chr1 - 229489771 229489771 229489771 CCCCTTCCAGGTTCAAGTGGTTCTCCTGCCTCAGCCTCCCGAGTGGCTGGGACTGTAGGCATGTG CCCCTTCCAGGTTCAAGTGGTTCTCCTGCCTCGGCCTCCCGAGTGGCTGGGACTGTAGGCATGTG T C NUP133 Ensembl:ENSG00000069248 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs897334658 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_648,RMVar_hsa_circ_91523,RMVar_hsa_circ_95693,RMVar_hsa_circ_24928,RMVar_hsa_circ_140259,RMVar_hsa_circ_140260,RMVar_hsa_circ_73674,RMVar_hsa_circ_44670,RMVar_hsa_circ_99295,RMVar_hsa_circ_352201,RMVar_hsa_circ_366436,RMVar_hsa_circ_125731,RMVar_hsa_circ_103300,RMVar_hsa_circ_77689,RMVar_hsa_circ_140284,RMVar_hsa_circ_140285,RMVar_hsa_circ_140283,RMVar_hsa_circ_374880,RMVar_hsa_circ_91370,RMVar_hsa_circ_140297,RMVar_hsa_circ_22321,RMVar_hsa_circ_140298,RMVar_hsa_circ_140296,RMVar_hsa_circ_306511,RMVar_hsa_circ_140301,RMVar_hsa_circ_12226,RMVar_hsa_circ_321461,RMVar_hsa_circ_122999,RMVar_hsa_circ_140306,RMVar_hsa_circ_288594,RMVar_hsa_circ_346650,RMVar_hsa_circ_335368,RMVar_hsa_circ_59230,RMVar_hsa_circ_140307,RMVar_hsa_circ_140308,RMVar_hsa_circ_272070,RMVar_hsa_circ_376854,RMVar_hsa_circ_377731,RMVar_hsa_circ_140309,RMVar_hsa_circ_377203,RMVar_hsa_circ_267005,RMVar_hsa_circ_140314,RMVar_hsa_circ_140311,RMVar_hsa_circ_140312,RMVar_hsa_circ_140313 28108 RMVar_ID_28108 Human_SNP_ID_52875773 A-to-I Human chr1 - 229552793 229552793 229552793 TCTCTGTGTTCGAGATTCCTCTCTGAAAAACGAGGATAAGATGAGGGTGAAAGGGAGGATTTAAG TCTCTGTGTTCGAGATTCCTCTCTGAAAAACGTGGATAAGATGAGGGTGAAAGGGAGGATTTAAG T A ABCB10 Ensembl:ENSG00000135776 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1275098178 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557442 28109 RMVar_ID_28109 Human_SNP_ID_52880304 A-to-I Human chr1 + 229570161 229570161 229570161 GGGGCATGCTACCACGCCCGGCTAATTTTTGTATTTTTAGTAGAGATGAGGGTTCACCATATTGG GGGGCATGCTACCACGCCCGGCTAATTTTTGTGTTTTTAGTAGAGATGAGGGTTCACCATATTGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs898672435 Functional Loss SNV dbSNP153 33..33 33 - - - 28110 RMVar_ID_28110 Human_SNP_ID_53011540 A-to-I Human chr1 + 230094025 230094025 230094025 GTTTCGTCCACCTGTGTGTGTGTGTTTGAGATAGGGTCTCGCTCTGTTGCCCAGGCTGGAATGCA GTTTCGTCCACCTGTGTGTGTGTGTTTGAGATGGGGTCTCGCTCTGTTGCCCAGGCTGGAATGCA A G GALNT2 Ensembl:ENSG00000143641 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1183898547 Functional Loss SNV dbSNP153 33..33 33 - - - 28111 RMVar_ID_28111 Human_SNP_ID_53020830 A-to-I Human chr1 - 230130473 230130473 230130473 CCTTGAAGCACCTCATCCAACAGTGGGGGTAAACACCAGGCTCCCAAACCCTTCACAACCGGCTG CCTTGAAGCACCTCATCCAACAGTGGGGGTAAGCACCAGGCTCCCAAACCCTTCACAACCGGCTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs532563552 Functional Loss SNV dbSNP153 33..33 33 - - - 28112 RMVar_ID_28112 Human_SNP_ID_53045112 A-to-I Human chr1 + 230228232 230228232 230228232 ATCCAGTATTGTAGAAATATTAATTTCCTTCAAATTAACTCATAAATTCAGTGCAGTGTCATGCA ATCCAGTATTGTAGAAATATTAATTTCCTTCACATTAACTCATAAATTCAGTGCAGTGTCATGCA A C GALNT2 Ensembl:ENSG00000143641 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs773286177 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55429,RMVar_hsa_circ_361088,RMVar_hsa_circ_340437,RMVar_hsa_circ_72993,RMVar_hsa_circ_140351 28113 RMVar_ID_28113 Human_SNP_ID_53045113 A-to-I Human chr1 + 230228232 230228232 230228232 ATCCAGTATTGTAGAAATATTAATTTCCTTCAAATTAACTCATAAATTCAGTGCAGTGTCATGCA ATCCAGTATTGTAGAAATATTAATTTCCTTCAGATTAACTCATAAATTCAGTGCAGTGTCATGCA A G GALNT2 Ensembl:ENSG00000143641 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs773286177 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55429,RMVar_hsa_circ_361088,RMVar_hsa_circ_340437,RMVar_hsa_circ_72993,RMVar_hsa_circ_140351 28114 RMVar_ID_28114 Human_SNP_ID_53079652 A-to-I Human chr1 - 230357118 230357118 230357118 AGGCGTTCCTGGGCTACATGATCTCCACCAGCATCTCCCACTGCGAGTCCGTCCTCAGCATCTGG AGGCGTTCCTGGGCTACATGATCTCCACCAGCGTCTCCCACTGCGAGTCCGTCCTCAGCATCTGG T C PGBD5 Ensembl:ENSG00000177614 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1042307412 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_62248,RMVar_hsa_circ_343534,RMVar_hsa_circ_284937,RMVar_hsa_circ_343558,RMVar_hsa_circ_140373 28115 RMVar_ID_28115 Human_SNP_ID_53229951 A-to-I Human chr1 - 230968477 230968477 230968477 ATCCTGCCTTCTTAGTTTAATGCTAAGAAGAAAGGGAATAAATGAACTAGATGCTGAACTTGAGC ATCCTGCCTTCTTAGTTTAATGCTAAGAAGAAGGGGAATAAATGAACTAGATGCTGAACTTGAGC T C TTC13 Ensembl:ENSG00000143643 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1258608724 Functional Loss SNV dbSNP153 33..33 33 - - - 28116 RMVar_ID_28116 Human_SNP_ID_53233063 A-to-I Human chr1 + 230980537 230980537 230980537 TTTTGTATTTTTAGTAGAGACCAGGTTTCACCATGTTGACCAGGCTGGTCTTGAACTGACCTCAA TTTTGTATTTTTAGTAGAGACCAGGTTTCACCGTGTTGACCAGGCTGGTCTTGAACTGACCTCAA A G ARV1 Ensembl:ENSG00000173409 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1326710550 Functional Loss SNV dbSNP153 33..33 33 - - - 28117 RMVar_ID_28117 Human_SNP_ID_53236216 A-to-I Human chr1 + 230993279 230993278 230993279 TGCCTGGCTAATTTAAAAAAAAAAATTTATGTAAAGGCAGTATCTTACTCTGTTGTCCAGGTTGG TGCCTGGCTAATTTAAAAAAAAAAATTTATGT_AAGGCAGTATCTTACTCTGTTGTCCAGGTTGG TA T ARV1 Ensembl:ENSG00000173409 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1193859718 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_1528,RMVar_hsa_circ_328564 28118 RMVar_ID_28118 Human_SNP_ID_53236217 A-to-I Human chr1 + 230993280 230993280 230993280 GCCTGGCTAATTTAAAAAAAAAAATTTATGTAAAGGCAGTATCTTACTCTGTTGTCCAGGTTGGT GCCTGGCTAATTTAAAAAAAAAAATTTATGTAGAGGCAGTATCTTACTCTGTTGTCCAGGTTGGT A G ARV1 Ensembl:ENSG00000173409 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1343453792 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1528,RMVar_hsa_circ_328564 28119 RMVar_ID_28119 Human_SNP_ID_53236218 A-to-I Human chr1 + 230993293 230993293 230993293 AAAAAAAAAAATTTATGTAAAGGCAGTATCTTACTCTGTTGTCCAGGTTGGTCTTGAACTCCTGG AAAAAAAAAAATTTATGTAAAGGCAGTATCTTCCTCTGTTGTCCAGGTTGGTCTTGAACTCCTGG A C ARV1 Ensembl:ENSG00000173409 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs770492187 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1528,RMVar_hsa_circ_328564 28120 RMVar_ID_28120 Human_SNP_ID_53242650 A-to-I Human chr1 - 231019575 231019574 231019576 ACCTGCTGGGGATTCATAATGAGAATATAACAAGAGGATCTCGGTGAAAGGCCTTAGTGGGTGTT ACCTGCTGGGGATTCATAATGAGAATATAAC__GAGGATCTCGGTGAAAGGCCTTAGTGGGTGTT CTT C FAM89A Ensembl:ENSG00000182118 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1293984253 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_345639,Human_RBP_ID_975977,Human_RBP_ID_4032052,Human_RBP_ID_5777109,Human_RBP_ID_10835328,Human_RBP_ID_17676965,Human_RBP_ID_17742665,Human_RBP_ID_18225995,Human_RBP_ID_27177874,Human_RBP_ID_27589487 28121 RMVar_ID_28121 Human_SNP_ID_53321544 A-to-I Human chr1 - 231330652 231330652 231330652 CTGTATCGCCCAGGCTGGAGTGCGATGGTGCTATCATGCCTCATTGTAGCCTCAACCTCCCTGGC CTGTATCGCCCAGGCTGGAGTGCGATGGTGCTGTCATGCCTCATTGTAGCCTCAACCTCCCTGGC T C lnc-EXOC8-1 RNACentral:URS00008BEC00 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs899928529 Functional Loss SNV dbSNP153 33..33 33 - - - 28122 RMVar_ID_28122 Human_SNP_ID_53321636 A-to-I Human chr1 - 231330954 231330954 231330954 AGACCCCCGTCTTTACAAAAAATAGAAAAATTAGCCGGGCGTGGTGGCGCACACCTGTAAGTCCC AGACCCCCGTCTTTACAAAAAATAGAAAAATTTGCCGGGCGTGGTGGCGCACACCTGTAAGTCCC T A lnc-EXOC8-1 RNACentral:URS00008BEC00 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs757823475 Functional Loss SNV dbSNP153 33..33 33 - - - 28123 RMVar_ID_28123 Human_SNP_ID_53321659 A-to-I Human chr1 - 231331041 231331039 231331042 CAAGTCTGTAATCCCAACACTTTGGCAGGCTAAGGAGAGTGGATTGCTTAAGCCCAGGAGTTCGA CAAGTCTGTAATCCCAACACTTTGGCAGGCT___GAGAGTGGATTGCTTAAGCCCAGGAGTTCGA CCTT C lnc-EXOC8-1 RNACentral:URS00008BEC00 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1284909263 Functional Loss DEL dbSNP153 32..34 33 - - - 28124 RMVar_ID_28124 Human_SNP_ID_53325961 A-to-I Human chr1 + 231346685 231346685 231346685 AAAGTTTTGTCTGGGTGCAGTGGCTGACGCCTATAATCCCAGCACTTTGGGAGGCTGAGGCGGGC AAAGTTTTGTCTGGGTGCAGTGGCTGACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGC A G SPRTN Ensembl:ENSG00000010072 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1291520952 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91860,RMVar_hsa_circ_140439 28125 RMVar_ID_28125 Human_SNP_ID_53343915 A-to-I Human chr1 - 231416641 231416641 231416641 TATTTTAGGCTGGGCTTTAGTGGCTCACGCCTATAATCCCAGCATTTTGAGGGGCTGAGGCAGGA TATTTTAGGCTGGGCTTTAGTGGCTCACGCCTGTAATCCCAGCATTTTGAGGGGCTGAGGCAGGA T C EGLN1,AL445524.2 Ensembl:ENSG00000135766,Ensembl:ENSG00000287856 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1440152116 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114195,RMVar_hsa_circ_140445 28126 RMVar_ID_28126 Human_SNP_ID_53379089 A-to-I Human chr1 + 231566864 231566864 231566864 TGTATTACATCAGTGAATTTTTTTATTTTTTTAGACTTAGTCTCTCTCTATTGCCCAGACTGGAG TGTATTACATCAGTGAATTTTTTTATTTTTTTTGACTTAGTCTCTCTCTATTGCCCAGACTGGAG A T TSNAX-DISC1 Ensembl:ENSG00000270106 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs753787195 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3302093,Human_RBP_ID_10839187 RMVar_hsa_circ_104896,RMVar_hsa_circ_121400,RMVar_hsa_circ_140447,RMVar_hsa_circ_140448,RMVar_hsa_circ_361903 28127 RMVar_ID_28127 Human_SNP_ID_53601246 A-to-I Human chr1 - 232490038 232490038 232490038 ATTAGGATGTGACGTGATCAGAGCTGTATTTTAGGAAGATTATTCTGGTAGAAGGGAATTGTACA ATTAGGATGTGACGTGATCAGAGCTGTATTTTGGGAAGATTATTCTGGTAGAAGGGAATTGTACA T C SIPA1L2 Ensembl:ENSG00000116991 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1332461534 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5779228 RMVar_hsa_circ_62918,RMVar_hsa_circ_323348,RMVar_hsa_circ_41667,RMVar_hsa_circ_93197,RMVar_hsa_circ_140476,RMVar_hsa_circ_140477,RMVar_hsa_circ_110252,RMVar_hsa_circ_342218,RMVar_hsa_circ_352773,RMVar_hsa_circ_365472 28128 RMVar_ID_28128 Human_SNP_ID_53695627 A-to-I Human chr1 - 232868629 232868629 232868629 CTCCTGCCTCAGCCTCCTGAGTAGCTAGGACTACAGGCGTGCGCCAGCTAATTTTTGTATTTTTA CTCCTGCCTCAGCCTCCTGAGTAGCTAGGACTGCAGGCGTGCGCCAGCTAATTTTTGTATTTTTA T C lnc-PCNX2-8 RNACentral:URS0000D5B477 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1286134570 Functional Loss SNV dbSNP153 33..33 33 - - - 28129 RMVar_ID_28129 Human_SNP_ID_53717651 A-to-I Human chr1 + 232960116 232960116 232960116 ACATGCCCGTGTCCCAGGTACTCAGGAGGCTGAAGCAGGAGAATCGCTTGAACCCAGGAAGCAGA ACATGCCCGTGTCCCAGGTACTCAGGAGGCTGGAGCAGGAGAATCGCTTGAACCCAGGAAGCAGA A G NTPCR Ensembl:ENSG00000135778 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1160111245 Functional Loss SNV dbSNP153 33..33 33 - - - 28130 RMVar_ID_28130 Human_SNP_ID_53746648 A-to-I Human chr1 - 233086305 233086305 233086305 TAAATTTAAATAGCCACCTGTGATGGGAGGCTACCATATTGGAAAGCACAGATATAGACCCTTCT TAAATTTAAATAGCCACCTGTGATGGGAGGCTGCCATATTGGAAAGCACAGATATAGACCCTTCT T C PCNX2 Ensembl:ENSG00000135749 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1208023753 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2219,RMVar_hsa_circ_75934,RMVar_hsa_circ_80113,RMVar_hsa_circ_85264,RMVar_hsa_circ_140487,RMVar_hsa_circ_370343,RMVar_hsa_circ_117173,RMVar_hsa_circ_140490,RMVar_hsa_circ_140491,RMVar_hsa_circ_91439,RMVar_hsa_circ_113594,RMVar_hsa_circ_140493,RMVar_hsa_circ_140495,RMVar_hsa_circ_81895,RMVar_hsa_circ_140494,RMVar_hsa_circ_140492,RMVar_hsa_circ_324199,RMVar_hsa_circ_378777,RMVar_hsa_circ_140496,RMVar_hsa_circ_140502,RMVar_hsa_circ_96071,RMVar_hsa_circ_97696,RMVar_hsa_circ_76957,RMVar_hsa_circ_105697,RMVar_hsa_circ_140504,RMVar_hsa_circ_140505,RMVar_hsa_circ_140503,RMVar_hsa_circ_267179,RMVar_hsa_circ_26396,RMVar_hsa_circ_140508,RMVar_hsa_circ_12377,RMVar_hsa_circ_321569,RMVar_hsa_circ_365762,RMVar_hsa_circ_374338,RMVar_hsa_circ_374339,RMVar_hsa_circ_321736,RMVar_hsa_circ_301125,RMVar_hsa_circ_275025,RMVar_hsa_circ_52052,RMVar_hsa_circ_59902,RMVar_hsa_circ_24513,RMVar_hsa_circ_140518,RMVar_hsa_circ_140511,RMVar_hsa_circ_140513,RMVar_hsa_circ_140514,RMVar_hsa_circ_140512,RMVar_hsa_circ_119558,RMVar_hsa_circ_140510,RMVar_hsa_circ_76435,RMVar_hsa_circ_140517 28131 RMVar_ID_28131 Human_SNP_ID_53780025 A-to-I Human chr1 - 233227234 233227234 233227234 GTCTGGTATGATCGACTGACCTTGCTGGCATTACTTGATCGGTAAGCCACTGAGCATGCACACAC GTCTGGTATGATCGACTGACCTTGCTGGCATTGCTTGATCGGTAAGCCACTGAGCATGCACACAC T C PCNX2 Ensembl:ENSG00000135749 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1230405319 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_199321,Human_Splice_Rec_199551,Human_Splice_Rec_199569,Human_Splice_Rec_199575 Human_miRNA_ID_2009267,Human_miRNA_ID_2009268,Human_miRNA_ID_2281003,Human_miRNA_ID_2281004,Human_miRNA_ID_2282567,Human_miRNA_ID_2282568,Human_miRNA_ID_2630613,Human_miRNA_ID_2630614 RMVar_hsa_circ_2219,RMVar_hsa_circ_80113,RMVar_hsa_circ_140491,RMVar_hsa_circ_91439,RMVar_hsa_circ_140495,RMVar_hsa_circ_81895,RMVar_hsa_circ_140494,RMVar_hsa_circ_96071,RMVar_hsa_circ_105697,RMVar_hsa_circ_140503,RMVar_hsa_circ_140508,RMVar_hsa_circ_321736,RMVar_hsa_circ_59902,RMVar_hsa_circ_24513,RMVar_hsa_circ_79160,RMVar_hsa_circ_289734,RMVar_hsa_circ_329870,RMVar_hsa_circ_82991,RMVar_hsa_circ_34120,RMVar_hsa_circ_140519,RMVar_hsa_circ_140520,RMVar_hsa_circ_116689,RMVar_hsa_circ_140529,RMVar_hsa_circ_140530,RMVar_hsa_circ_312075,RMVar_hsa_circ_353934,RMVar_hsa_circ_292224,RMVar_hsa_circ_300009,RMVar_hsa_circ_91869,RMVar_hsa_circ_302044,RMVar_hsa_circ_140535,RMVar_hsa_circ_317864,RMVar_hsa_circ_334152,RMVar_hsa_circ_353143,RMVar_hsa_circ_140546,RMVar_hsa_circ_140547,RMVar_hsa_circ_140545,RMVar_hsa_circ_50122,RMVar_hsa_circ_6436,RMVar_hsa_circ_140559,RMVar_hsa_circ_282141,RMVar_hsa_circ_335597,RMVar_hsa_circ_12358,RMVar_hsa_circ_277552,RMVar_hsa_circ_140549,RMVar_hsa_circ_140548,RMVar_hsa_circ_270668,RMVar_hsa_circ_301694,RMVar_hsa_circ_370236,RMVar_hsa_circ_301856,RMVar_hsa_circ_90234,RMVar_hsa_circ_79200,RMVar_hsa_circ_140560,RMVar_hsa_circ_140555,RMVar_hsa_circ_140557,RMVar_hsa_circ_140558,RMVar_hsa_circ_140556,RMVar_hsa_circ_115276,RMVar_hsa_circ_140554,RMVar_hsa_circ_359794,RMVar_hsa_circ_281798,RMVar_hsa_circ_335560,RMVar_hsa_circ_140567,RMVar_hsa_circ_369426,RMVar_hsa_circ_274228,RMVar_hsa_circ_99525,RMVar_hsa_circ_110396,RMVar_hsa_circ_140569,RMVar_hsa_circ_140570,RMVar_hsa_circ_140571,RMVar_hsa_circ_307577,RMVar_hsa_circ_370535,RMVar_hsa_circ_280463,RMVar_hsa_circ_140575,RMVar_hsa_circ_88340,RMVar_hsa_circ_104532,RMVar_hsa_circ_140577,RMVar_hsa_circ_140578,RMVar_hsa_circ_140576,RMVar_hsa_circ_140573,RMVar_hsa_circ_140574,RMVar_hsa_circ_342183,RMVar_hsa_circ_371058,RMVar_hsa_circ_109360,RMVar_hsa_circ_140587,RMVar_hsa_circ_140580,RMVar_hsa_circ_140582,RMVar_hsa_circ_140583,RMVar_hsa_circ_140581,RMVar_hsa_circ_286424,RMVar_hsa_circ_346605,RMVar_hsa_circ_348940,RMVar_hsa_circ_316241,RMVar_hsa_circ_119803,RMVar_hsa_circ_140585,RMVar_hsa_circ_140586,RMVar_hsa_circ_140584 28132 RMVar_ID_28132 Human_SNP_ID_53784848 A-to-I Human chr1 - 233247924 233247924 233247924 TTGGTCTTAAGAGTTCTAGAAAAGGGCTGGGCATGGTGGCTCACACCTGCAATCTCAGCACTTTT TTGGTCTTAAGAGTTCTAGAAAAGGGCTGGGCCTGGTGGCTCACACCTGCAATCTCAGCACTTTT T G PCNX2 Ensembl:ENSG00000135749 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs898849201 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80113,RMVar_hsa_circ_140491,RMVar_hsa_circ_91439,RMVar_hsa_circ_140495,RMVar_hsa_circ_96071,RMVar_hsa_circ_105697,RMVar_hsa_circ_140503,RMVar_hsa_circ_140508,RMVar_hsa_circ_59902,RMVar_hsa_circ_24513,RMVar_hsa_circ_82991,RMVar_hsa_circ_34120,RMVar_hsa_circ_140519,RMVar_hsa_circ_353934,RMVar_hsa_circ_300009,RMVar_hsa_circ_91869,RMVar_hsa_circ_334152,RMVar_hsa_circ_353143,RMVar_hsa_circ_140547,RMVar_hsa_circ_6436,RMVar_hsa_circ_335597,RMVar_hsa_circ_370236,RMVar_hsa_circ_301856,RMVar_hsa_circ_90234,RMVar_hsa_circ_79200,RMVar_hsa_circ_140555,RMVar_hsa_circ_140557,RMVar_hsa_circ_140556,RMVar_hsa_circ_140554,RMVar_hsa_circ_335560,RMVar_hsa_circ_369426,RMVar_hsa_circ_99525,RMVar_hsa_circ_110396,RMVar_hsa_circ_140571,RMVar_hsa_circ_370535,RMVar_hsa_circ_140575,RMVar_hsa_circ_88340,RMVar_hsa_circ_104532,RMVar_hsa_circ_140576,RMVar_hsa_circ_140573,RMVar_hsa_circ_140574,RMVar_hsa_circ_371058,RMVar_hsa_circ_140587,RMVar_hsa_circ_140582,RMVar_hsa_circ_140583,RMVar_hsa_circ_346605,RMVar_hsa_circ_348940,RMVar_hsa_circ_316241,RMVar_hsa_circ_140586,RMVar_hsa_circ_374493,RMVar_hsa_circ_377076,RMVar_hsa_circ_343564,RMVar_hsa_circ_140589,RMVar_hsa_circ_140591,RMVar_hsa_circ_140590 28133 RMVar_ID_28133 Human_SNP_ID_53875989 A-to-I Human chr1 + 233616823 233616823 233616823 ATTATCATAGGTGCCCTGGCCATGAATCTTATAATGGGTGAGAAATCTTTTCTTCCCTACAAGGG ATTATCATAGGTGCCCTGGCCATGAATCTTATGATGGGTGAGAAATCTTTTCTTCCCTACAAGGG A G KCNK1 Ensembl:ENSG00000135750 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1249819150 Functional Loss SNV dbSNP153 33..33 33 - - - 28134 RMVar_ID_28134 Human_SNP_ID_53876121 A-to-I Human chr1 + 233617439 233617439 233617439 TTGTAGGAAAGAAAAGATTTCTCACCCATCATAAGGTTCATGGCCGGGGAACTTATAATAAAATG TTGTAGGAAAGAAAAGATTTCTCACCCATCATGAGGTTCATGGCCGGGGAACTTATAATAAAATG A G KCNK1 Ensembl:ENSG00000135750 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs114525498 Functional Loss SNV dbSNP153 33..33 33 - - - 28135 RMVar_ID_28135 Human_SNP_ID_53876215 A-to-I Human chr1 + 233617819 233617819 233617819 AAAATTAGCCCGGAGTGATGGCGTGTGCCTGTAGTCCCAGCTACCTAGAAGGCTGAGGCATTGAG AAAATTAGCCCGGAGTGATGGCGTGTGCCTGTCGTCCCAGCTACCTAGAAGGCTGAGGCATTGAG A C KCNK1 Ensembl:ENSG00000135750 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs143991053 Functional Loss SNV dbSNP153 33..33 33 - - - 28136 RMVar_ID_28136 Human_SNP_ID_53876216 A-to-I Human chr1 + 233617819 233617819 233617819 AAAATTAGCCCGGAGTGATGGCGTGTGCCTGTAGTCCCAGCTACCTAGAAGGCTGAGGCATTGAG AAAATTAGCCCGGAGTGATGGCGTGTGCCTGTGGTCCCAGCTACCTAGAAGGCTGAGGCATTGAG A G KCNK1 Ensembl:ENSG00000135750 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs143991053 Functional Loss SNV dbSNP153 33..33 33 - - - 28137 RMVar_ID_28137 Human_SNP_ID_53884465 A-to-I Human chr1 + 233651926 233651926 233651926 TCACATGAGGTTGTATAAACCCTCTTATTCCTATTCTCATGGAATTGGGAACAGGAAGACAAGGG TCACATGAGGTTGTATAAACCCTCTTATTCCTCTTCTCATGGAATTGGGAACAGGAAGACAAGGG A C KCNK1 Ensembl:ENSG00000135750 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1336957496 Functional Loss SNV dbSNP153 33..33 33 - - - 28138 RMVar_ID_28138 Human_SNP_ID_53888752 A-to-I Human chr1 + 233669619 233669619 233669619 CCTGTAATCATAGTACTTTGGGAGACGAAGGCAGGCAGATCACTAAGGCCAGGAGTTCGAGACCA CCTGTAATCATAGTACTTTGGGAGACGAAGGCGGGCAGATCACTAAGGCCAGGAGTTCGAGACCA A G KCNK1 Ensembl:ENSG00000135750 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs765463431 Functional Loss SNV dbSNP153 33..33 33 - - - 28139 RMVar_ID_28139 Human_SNP_ID_54045473 A-to-I Human chr1 + 234325678 234325678 234325678 AAAATCTGAGCCAGGTGTAGTGGCTCACACCCATAATCCCAGCACTTTGGGAGGTGGAGGCAGGA AAAATCTGAGCCAGGTGTAGTGGCTCACACCCGTAATCCCAGCACTTTGGGAGGTGGAGGCAGGA A G - - Other Unknown GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1230290953 Functional Loss SNV dbSNP153 33..33 33 - - - 28140 RMVar_ID_28140 Human_SNP_ID_54054025 A-to-I Human chr1 + 234360272 234360272 234360272 CCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCCTTTGAACCCGGTGGGTGGAGGTT CCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCTGGAGAATCCTTTGAACCCGGTGGGTGGAGGTT A T AL355472.2 Ensembl:ENSG00000236358 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs911031309 Functional Loss SNV dbSNP153 33..33 33 - - - 28141 RMVar_ID_28141 Human_SNP_ID_54054688 A-to-I Human chr1 + 234363179 234363179 234363179 GGAGATCGAGACCATTTTGGCCAACATGTTGAAACTCCGTGTCTACTAAAATACAAAATAAAAAT GGAGATCGAGACCATTTTGGCCAACATGTTGATACTCCGTGTCTACTAAAATACAAAATAAAAAT A T AL355472.2 Ensembl:ENSG00000236358 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs918631947 Functional Loss SNV dbSNP153 33..33 33 - - - 28142 RMVar_ID_28142 Human_SNP_ID_54054714 A-to-I Human chr1 + 234363275 234363275 234363275 CTAGCTACTTGGGAGACTGAGGCTGGGGAATCACCTGAACTCCGGAGGTGGAGGTTGCAGTGAGC CTAGCTACTTGGGAGACTGAGGCTGGGGAATCGCCTGAACTCCGGAGGTGGAGGTTGCAGTGAGC A G AL355472.2 Ensembl:ENSG00000236358 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1236633527 Functional Loss SNV dbSNP153 33..33 33 - - - 28143 RMVar_ID_28143 Human_SNP_ID_54055808 A-to-I Human chr1 + 234366979 234366979 234366979 GCTGGGCAGGAGAATGACTTGAACCCGGGAGGAAGAGGTTGCAGTGAGCTGAGATCGGGCCACTG GCTGGGCAGGAGAATGACTTGAACCCGGGAGGCAGAGGTTGCAGTGAGCTGAGATCGGGCCACTG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560632596 Functional Loss SNV dbSNP153 33..33 33 - - - 28144 RMVar_ID_28144 Human_SNP_ID_54058796 A-to-I Human chr1 + 234377368 234377368 234377368 AGGCTGGTCTTGAACTCCTGACCTCTTGTTCCACCCGCCTCAGCCTCCCAAAGTGCTGGGATTAC AGGCTGGTCTTGAACTCCTGACCTCTTGTTCCCCCCGCCTCAGCCTCCCAAAGTGCTGGGATTAC A C COA6 Ensembl:ENSG00000168275 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs979153774 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99846,RMVar_hsa_circ_140609 28145 RMVar_ID_28145 Human_SNP_ID_54059221 A-to-I Human chr1 + 234379114 234379114 234379114 GTTGCCCAGGCTGGTCTTGAACTCCTGGACTCAAGCGATCTGCCCATCTCAGCCTCCCAAAGAGC GTTGCCCAGGCTGGTCTTGAACTCCTGGACTCCAGCGATCTGCCCATCTCAGCCTCCCAAAGAGC A C COA6 Ensembl:ENSG00000168275 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978167781 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99846,RMVar_hsa_circ_140609 28146 RMVar_ID_28146 Human_SNP_ID_54062662 A-to-I Human chr1 - 234392505 234392494 234392505 CTAATTGATTATCTGCAGCAGAAGAAAACAGAAGGTTATACCATCATTGGAGTGGAACAAACTGC CTAATTGATTATCTGCAGCAGAAGAAAACAGA___________TCATTGGAGTGGAACAAACTGC ATGGTATAACCT A TARBP1 Ensembl:ENSG00000059588 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1173805054 Functional Loss DEL dbSNP153 33..43 33 - - - Human_RBP_ID_346436,Human_RBP_ID_1740599,Human_RBP_ID_18566969 Human_Splice_Rec_199766,Human_Splice_Rec_199767,Human_Splice_Rec_199778,Human_Splice_Rec_199779,Human_Splice_Rec_199792,Human_Splice_Rec_199793,Human_Splice_Rec_199800,Human_Splice_Rec_199801,Human_Splice_Rec_199803 RMVar_hsa_circ_83641,RMVar_hsa_circ_54777,RMVar_hsa_circ_140610,RMVar_hsa_circ_266104 28147 RMVar_ID_28147 Human_SNP_ID_54062665 A-to-I Human chr1 - 234392505 234392499 234392505 CTAATTGATTATCTGCAGCAGAAGAAAACAGAAGGTTATACCATCATTGGAGTGGAACAAACTGC CTAATTGATTATCTGCAGCAGAAGAAAACAGA______TACCATCATTGGAGTGGAACAAACTGC ATAACCT A TARBP1 Ensembl:ENSG00000059588 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs758207258 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_346436,Human_RBP_ID_1740599,Human_RBP_ID_18566969 Human_Splice_Rec_199766,Human_Splice_Rec_199767,Human_Splice_Rec_199778,Human_Splice_Rec_199779,Human_Splice_Rec_199792,Human_Splice_Rec_199793,Human_Splice_Rec_199800,Human_Splice_Rec_199801,Human_Splice_Rec_199803 RMVar_hsa_circ_83641,RMVar_hsa_circ_54777,RMVar_hsa_circ_140610,RMVar_hsa_circ_266104 28148 RMVar_ID_28148 Human_SNP_ID_54062667 A-to-I Human chr1 - 234392505 234392505 234392505 CTAATTGATTATCTGCAGCAGAAGAAAACAGAAGGTTATACCATCATTGGAGTGGAACAAACTGC CTAATTGATTATCTGCAGCAGAAGAAAACAGAGGGTTATACCATCATTGGAGTGGAACAAACTGC T C TARBP1 Ensembl:ENSG00000059588 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs148238545 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_346436,Human_RBP_ID_1740599,Human_RBP_ID_18566969 Human_Splice_Rec_199766,Human_Splice_Rec_199767,Human_Splice_Rec_199778,Human_Splice_Rec_199779,Human_Splice_Rec_199792,Human_Splice_Rec_199793,Human_Splice_Rec_199800,Human_Splice_Rec_199801,Human_Splice_Rec_199803 RMVar_hsa_circ_83641,RMVar_hsa_circ_54777,RMVar_hsa_circ_140610,RMVar_hsa_circ_266104 28149 RMVar_ID_28149 Human_SNP_ID_54067210 A-to-I Human chr1 - 234408265 234408265 234408265 TAGGTCAGATCTCTTTCCCCACCTCAGTTACAATTTTGCAAAGGCGGTTTCAGAATCAGAGCACG TAGGTCAGATCTCTTTCCCCACCTCAGTTACAGTTTTGCAAAGGCGGTTTCAGAATCAGAGCACG T C TARBP1 Ensembl:ENSG00000059588 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1028585083 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9560370,Human_RBP_ID_10845688,Human_RBP_ID_24657028 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 28150 RMVar_ID_28150 Human_SNP_ID_54139018 A-to-I Human chr1 - 234689010 234689010 234689010 TCTGCCTCAGCCTCCGAAGTAGCTAGGCTTACAGACACGTGCCACCACACCCTGCCAATTTTTGT TCTGCCTCAGCCTCCGAAGTAGCTAGGCTTACGGACACGTGCCACCACACCCTGCCAATTTTTGT T C AL160408.3 Ensembl:ENSG00000230628 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1235821736 Functional Loss SNV dbSNP153 33..33 33 - - - 28151 RMVar_ID_28151 Human_SNP_ID_54242975 A-to-I Human chr1 - 235105639 235105639 235105639 GCATGTGCCACCATGTACAAATACATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGG GCATGTGCCACCATGTACAAATACATTTTTGTGTTTTTAGTAGAGACAGGGTTTCACCATGTTGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs989785908 Functional Loss SNV dbSNP153 33..33 33 - - - 28152 RMVar_ID_28152 Human_SNP_ID_54243363 A-to-I Human chr1 - 235106904 235106904 235106904 GCATTCATAAAGGTTTTTGTTTTGTTTTTTTGAGACAGTCTGCTCTGTCGCCCAGGCTGGAGTGC GCATTCATAAAGGTTTTTGTTTTGTTTTTTTGGGACAGTCTGCTCTGTCGCCCAGGCTGGAGTGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs558838295 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2133649,Human_RBP_ID_5782601,Human_RBP_ID_8303161,Human_RBP_ID_10848282 28153 RMVar_ID_28153 Human_SNP_ID_54245299 A-to-I Human chr1 - 235114962 235114962 235114962 GGGAGGTTGAGGTGGGAGGATTGCTTGAGCCCAGGAGGTTGAGGCTGCAGTCAGCCAAGATTGTA GGGAGGTTGAGGTGGGAGGATTGCTTGAGCCCGGGAGGTTGAGGCTGCAGTCAGCCAAGATTGTA T C TOMM20 Ensembl:ENSG00000173726 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559001861 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97201,RMVar_hsa_circ_126493,RMVar_hsa_circ_140668,RMVar_hsa_circ_307952,RMVar_hsa_circ_140667 28154 RMVar_ID_28154 Human_SNP_ID_54245313 A-to-I Human chr1 - 235115010 235115010 235115010 GCAAAATTAGCCCGGTGTGGTGGTGCACACCTATGGTCCTAGCTACTTGGGAGGTTGAGGTGGGA GCAAAATTAGCCCGGTGTGGTGGTGCACACCTGTGGTCCTAGCTACTTGGGAGGTTGAGGTGGGA T C TOMM20 Ensembl:ENSG00000173726 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs761862511 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97201,RMVar_hsa_circ_126493,RMVar_hsa_circ_140668,RMVar_hsa_circ_307952,RMVar_hsa_circ_140667 28155 RMVar_ID_28155 Human_SNP_ID_54247146 A-to-I Human chr1 - 235120945 235120945 235120945 TGCCCGCCTTGGACTCCCAATGTGCTGGGATTACAGGCATGAGCCACCGCACCCAGCTACTGAAG TGCCCGCCTTGGACTCCCAATGTGCTGGGATTCCAGGCATGAGCCACCGCACCCAGCTACTGAAG T G TOMM20 Ensembl:ENSG00000173726 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1475217875 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126493,RMVar_hsa_circ_307952,RMVar_hsa_circ_140667 28156 RMVar_ID_28156 Human_SNP_ID_54247717 A-to-I Human chr1 - 235123399 235123399 235123399 CTCACTGCAACCTCCGCCTCCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGG CTCACTGCAACCTCCGCCTCCCGGGTTCAAGCCATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGG T G TOMM20 Ensembl:ENSG00000173726 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1351899699 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126493,RMVar_hsa_circ_140667 28157 RMVar_ID_28157 Human_SNP_ID_54247742 A-to-I Human chr1 - 235123479 235123478 235123480 GTCTACAGGTAGGGAGACCTCTTTTTTGAGACAGAGTGTCGCTCTGTTGCCCAGGCTGAAGTGCA GTCTACAGGTAGGGAGACCTCTTTTTTGAGA__GAGTGTCGCTCTGTTGCCCAGGCTGAAGTGCA CTG C TOMM20 Ensembl:ENSG00000173726 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs954568769 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_5782937,Human_RBP_ID_10849046,Human_RBP_ID_19307864 RMVar_hsa_circ_126493,RMVar_hsa_circ_140667 28158 RMVar_ID_28158 Human_SNP_ID_54247905 A-to-I Human chr1 - 235124225 235124225 235124225 CTCTTGCTACAGCCTCTCGAGTAGCTAGGACTACAGGCGCCTGCCACCATACCTGGCTAATTTTT CTCTTGCTACAGCCTCTCGAGTAGCTAGGACTGCAGGCGCCTGCCACCATACCTGGCTAATTTTT T C TOMM20 Ensembl:ENSG00000173726 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs577963981 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10849104 RMVar_hsa_circ_126493,RMVar_hsa_circ_140667 28159 RMVar_ID_28159 Human_SNP_ID_54248140 A-to-I Human chr1 - 235125249 235125249 235125249 GATGACGCTGCTGCACTCCCGCCTGGGCGACAAAGCGAGACTCCGTCTCAAAAAGAAAAAAAATA GATGACGCTGCTGCACTCCCGCCTGGGCGACAGAGCGAGACTCCGTCTCAAAAAGAAAAAAAATA T C TOMM20 Ensembl:ENSG00000173726 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs920246792 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126493,RMVar_hsa_circ_140667 28160 RMVar_ID_28160 Human_SNP_ID_54248154 A-to-I Human chr1 - 235125293 235125293 235125293 GGAGAATGGCGTGAACTCGGGAGGCGGAGCTTACAGTGAGCCGAGATGACGCTGCTGCACTCCCG GGAGAATGGCGTGAACTCGGGAGGCGGAGCTTGCAGTGAGCCGAGATGACGCTGCTGCACTCCCG T C TOMM20 Ensembl:ENSG00000173726 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs893996565 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9499724,Human_RBP_ID_24760428 RMVar_hsa_circ_126493,RMVar_hsa_circ_140667 28161 RMVar_ID_28161 Human_SNP_ID_54248525 A-to-I Human chr1 - 235126349 235126349 235126349 AGGTGGGCGGATCACCTCATGTCAGGAGTTCAAGCAGCCTGGCCAGCATGGTGAAACCCCCACTC AGGTGGGCGGATCACCTCATGTCAGGAGTTCAGGCAGCCTGGCCAGCATGGTGAAACCCCCACTC T C TOMM20 Ensembl:ENSG00000173726 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350894219 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126493,RMVar_hsa_circ_140667 28162 RMVar_ID_28162 Human_SNP_ID_54248540 A-to-I Human chr1 - 235126404 235126404 235126404 ATTGAGGCTGGGTGTGGTGGCTCAACGCTAGTAATCTCAGCACTTTGGGAGGCCGAGGTGGGCGG ATTGAGGCTGGGTGTGGTGGCTCAACGCTAGTTATCTCAGCACTTTGGGAGGCCGAGGTGGGCGG T A TOMM20 Ensembl:ENSG00000173726 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs999952824 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22487407,Human_RBP_ID_23147575 RMVar_hsa_circ_126493,RMVar_hsa_circ_140667 28163 RMVar_ID_28163 Human_SNP_ID_54249012 A-to-I Human chr1 - 235128010 235128010 235128010 GTCACCACGCCCGGTGATTTTTTGTGTTTAGTAGAGACGGGGTTTCACCGTGTTGGTCAGGCTAG GTCACCACGCCCGGTGATTTTTTGTGTTTAGTGGAGACGGGGTTTCACCGTGTTGGTCAGGCTAG T C TOMM20 Ensembl:ENSG00000173726 Protein coding intron GSE107867 ASD brains,frontal_cortex;ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs931278276 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1740855,Human_RBP_ID_8303262,Human_RBP_ID_10849255 RMVar_hsa_circ_126493,RMVar_hsa_circ_140667 28164 RMVar_ID_28164 Human_SNP_ID_54249034 A-to-I Human chr1 - 235128092 235128092 235128092 TCGGCTCACTGCAACCTCCGCCTCCCGAGTTCAAGCGCTTCTCCTGCCTCAGTCTCCCCAGTAGC TCGGCTCACTGCAACCTCCGCCTCCCGAGTTCTAGCGCTTCTCCTGCCTCAGTCTCCCCAGTAGC T A TOMM20 Ensembl:ENSG00000173726 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs944291867 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8965333,Human_RBP_ID_10849255 RMVar_hsa_circ_126493,RMVar_hsa_circ_140667 28165 RMVar_ID_28165 Human_SNP_ID_54250670 A-to-I Human chr1 - 235133091 235133091 235133091 GTGATCTATCCGCCTTGGCCTCCCAGAGTGCTAGGATTATAGGTGTGAGCTACCCCGCCTGGCCT GTGATCTATCCGCCTTGGCCTCCCAGAGTGCTGGGATTATAGGTGTGAGCTACCCCGCCTGGCCT T C ARID4B,RBM34 Ensembl:ENSG00000054267,Ensembl:ENSG00000188739 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1184699320 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111668,RMVar_hsa_circ_140672,RMVar_hsa_circ_78458,RMVar_hsa_circ_140671 28166 RMVar_ID_28166 Human_SNP_ID_54250688 A-to-I Human chr1 - 235133169 235133169 235133169 TCTGGCTAATTCTTGTATTTTTTTGTAGAGACAGGATTCACCATGTTTCTCAGGCTGGTCTCCAA TCTGGCTAATTCTTGTATTTTTTTGTAGAGACGGGATTCACCATGTTTCTCAGGCTGGTCTCCAA T C ARID4B,RBM34 Ensembl:ENSG00000054267,Ensembl:ENSG00000188739 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1370042857 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111668,RMVar_hsa_circ_140672,RMVar_hsa_circ_78458,RMVar_hsa_circ_140671 28167 RMVar_ID_28167 Human_SNP_ID_54250716 A-to-I Human chr1 - 235133279 235133279 235133279 TGGAGTGCTTTGGCACGATCTCAGCTCACTGCAGCCTCTGCCTCCCAGGCTCTAGCGATCCTCCC TGGAGTGCTTTGGCACGATCTCAGCTCACTGCGGCCTCTGCCTCCCAGGCTCTAGCGATCCTCCC T C ARID4B,RBM34 Ensembl:ENSG00000054267,Ensembl:ENSG00000188739 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs972531363 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111668,RMVar_hsa_circ_140672,RMVar_hsa_circ_78458,RMVar_hsa_circ_140671 28168 RMVar_ID_28168 Human_SNP_ID_54250717 A-to-I Human chr1 - 235133279 235133279 235133279 TGGAGTGCTTTGGCACGATCTCAGCTCACTGCAGCCTCTGCCTCCCAGGCTCTAGCGATCCTCCC TGGAGTGCTTTGGCACGATCTCAGCTCACTGCCGCCTCTGCCTCCCAGGCTCTAGCGATCCTCCC T G ARID4B,RBM34 Ensembl:ENSG00000054267,Ensembl:ENSG00000188739 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs972531363 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111668,RMVar_hsa_circ_140672,RMVar_hsa_circ_78458,RMVar_hsa_circ_140671 28169 RMVar_ID_28169 Human_SNP_ID_54253201 A-to-I Human chr1 - 235142344 235142344 235142344 AACATGGGAGTTAGAGGTTGCAGTGAGCCGAGATCATGCCATTGCACTCCAGCCTGGACTGCAAG AACATGGGAGTTAGAGGTTGCAGTGAGCCGAGTTCATGCCATTGCACTCCAGCCTGGACTGCAAG T A ARID4B,RBM34 Ensembl:ENSG00000054267,Ensembl:ENSG00000188739 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1378026452 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111668,RMVar_hsa_circ_140674,RMVar_hsa_circ_65839,RMVar_hsa_circ_140672,RMVar_hsa_circ_304133,RMVar_hsa_circ_45021,RMVar_hsa_circ_140675,RMVar_hsa_circ_287600,RMVar_hsa_circ_140676 28170 RMVar_ID_28170 Human_SNP_ID_54253335 A-to-I Human chr1 - 235142876 235142876 235142876 GTCACCAGGCTGGAGTGCAGTGGTGCGATCCCAGCTCACTGCAACCTCCGCCTCCCGGGTTCAAC GTCACCAGGCTGGAGTGCAGTGGTGCGATCCCGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAC T C ARID4B,RBM34 Ensembl:ENSG00000054267,Ensembl:ENSG00000188739 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs890633749 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111668,RMVar_hsa_circ_140674,RMVar_hsa_circ_65839,RMVar_hsa_circ_140672,RMVar_hsa_circ_304133,RMVar_hsa_circ_45021,RMVar_hsa_circ_140675,RMVar_hsa_circ_287600,RMVar_hsa_circ_140676 28171 RMVar_ID_28171 Human_SNP_ID_54254088 A-to-I Human chr1 - 235145906 235145906 235145906 AGGCACGTGTCTGTAGTCCCAGCTACTTGGGAAGCTGACGTGAGATGATCACTTGAGCCCAGGAG AGGCACGTGTCTGTAGTCCCAGCTACTTGGGAGGCTGACGTGAGATGATCACTTGAGCCCAGGAG T C ARID4B,RBM34 Ensembl:ENSG00000054267,Ensembl:ENSG00000188739 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs940176239 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10849679 RMVar_hsa_circ_111668,RMVar_hsa_circ_140674,RMVar_hsa_circ_65839,RMVar_hsa_circ_140672,RMVar_hsa_circ_304133,RMVar_hsa_circ_45021,RMVar_hsa_circ_140675,RMVar_hsa_circ_287600,RMVar_hsa_circ_140676 28172 RMVar_ID_28172 Human_SNP_ID_54254367 A-to-I Human chr1 - 235147009 235147009 235147009 TCAGGCTGGTCTTGAACCCCGGGCTTCAAGCAATCCTTCTGCCTCAGCCTTCTAAAGCAGTGGGA TCAGGCTGGTCTTGAACCCCGGGCTTCAAGCAGTCCTTCTGCCTCAGCCTTCTAAAGCAGTGGGA T C ARID4B,RBM34 Ensembl:ENSG00000054267,Ensembl:ENSG00000188739 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs528207070 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11202259 RMVar_hsa_circ_111668,RMVar_hsa_circ_140674,RMVar_hsa_circ_65839,RMVar_hsa_circ_140672,RMVar_hsa_circ_304133,RMVar_hsa_circ_45021,RMVar_hsa_circ_140675,RMVar_hsa_circ_287600,RMVar_hsa_circ_140676 28173 RMVar_ID_28173 Human_SNP_ID_54255272 A-to-I Human chr1 - 235150253 235150253 235150253 CTGGCCAACATGGCAAAACTACGTTTCTACTAAAAATACGAAAACTAGCTGGGCATGGTGGCGGG CTGGCCAACATGGCAAAACTACGTTTCTACTAGAAATACGAAAACTAGCTGGGCATGGTGGCGGG T C ARID4B,RBM34 Ensembl:ENSG00000054267,Ensembl:ENSG00000188739 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs925883096 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24658199 RMVar_hsa_circ_55137,RMVar_hsa_circ_111668,RMVar_hsa_circ_65839,RMVar_hsa_circ_140672,RMVar_hsa_circ_304133,RMVar_hsa_circ_140675,RMVar_hsa_circ_287600,RMVar_hsa_circ_140676,RMVar_hsa_circ_295578,RMVar_hsa_circ_140677,RMVar_hsa_circ_140678 28174 RMVar_ID_28174 Human_SNP_ID_54255663 A-to-I Human chr1 - 235151798 235151798 235151798 AAACTCGTGACCTCAGGTGATTCGCCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG AAACTCGTGACCTCAGGTGATTCGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG T C ARID4B,RBM34 Ensembl:ENSG00000054267,Ensembl:ENSG00000188739 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1203270256 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11202280 RMVar_hsa_circ_55137,RMVar_hsa_circ_111668,RMVar_hsa_circ_65839,RMVar_hsa_circ_140672,RMVar_hsa_circ_304133,RMVar_hsa_circ_140675,RMVar_hsa_circ_287600,RMVar_hsa_circ_140676,RMVar_hsa_circ_295578,RMVar_hsa_circ_140677,RMVar_hsa_circ_140678 28175 RMVar_ID_28175 Human_SNP_ID_54255682 A-to-I Human chr1 - 235151853 235151853 235151853 AATTTTTGTATTTTTAGTCCGGACAGGGTTTCACCATGTTATCCAGACTGGTCTCAAACTCGTGA AATTTTTGTATTTTTAGTCCGGACAGGGTTTCGCCATGTTATCCAGACTGGTCTCAAACTCGTGA T C ARID4B,RBM34 Ensembl:ENSG00000054267,Ensembl:ENSG00000188739 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1300835226 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1424853,Human_RBP_ID_10849882 RMVar_hsa_circ_55137,RMVar_hsa_circ_111668,RMVar_hsa_circ_65839,RMVar_hsa_circ_140672,RMVar_hsa_circ_304133,RMVar_hsa_circ_140675,RMVar_hsa_circ_287600,RMVar_hsa_circ_140676,RMVar_hsa_circ_295578,RMVar_hsa_circ_140677,RMVar_hsa_circ_140678 28176 RMVar_ID_28176 Human_SNP_ID_54256177 A-to-I Human chr1 - 235153493 235153493 235153493 TTGAACCCAGGAGGGGGAGGTTGCAGAAGCCAAGATCGTGCCACCGCACTCCAGCCTGGGTGACA TTGAACCCAGGAGGGGGAGGTTGCAGAAGCCAGGATCGTGCCACCGCACTCCAGCCTGGGTGACA T C ARID4B,RBM34 Ensembl:ENSG00000054267,Ensembl:ENSG00000188739 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs561584610 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55137,RMVar_hsa_circ_111668,RMVar_hsa_circ_140672,RMVar_hsa_circ_304133,RMVar_hsa_circ_140675,RMVar_hsa_circ_287600,RMVar_hsa_circ_140676,RMVar_hsa_circ_295578,RMVar_hsa_circ_278108,RMVar_hsa_circ_140678,RMVar_hsa_circ_267527,RMVar_hsa_circ_140679 28177 RMVar_ID_28177 Human_SNP_ID_54256191 A-to-I Human chr1 - 235153562 235153562 235153562 AAATTAGCTGGGTGTGGTGACACATGCCTGTAATCCCAGCTACTTTGAAGGCTAAGGCAGGAGAA AAATTAGCTGGGTGTGGTGACACATGCCTGTACTCCCAGCTACTTTGAAGGCTAAGGCAGGAGAA T G ARID4B,RBM34 Ensembl:ENSG00000054267,Ensembl:ENSG00000188739 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs144690863 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55137,RMVar_hsa_circ_111668,RMVar_hsa_circ_140672,RMVar_hsa_circ_304133,RMVar_hsa_circ_140675,RMVar_hsa_circ_287600,RMVar_hsa_circ_140676,RMVar_hsa_circ_295578,RMVar_hsa_circ_278108,RMVar_hsa_circ_140678,RMVar_hsa_circ_267527,RMVar_hsa_circ_140679 28178 RMVar_ID_28178 Human_SNP_ID_54256331 A-to-I Human chr1 - 235154057 235154057 235154057 TATTTTTAGTAGAGACGGGGTTTCACTGTGCTAGCCAGGATGGTCTCGATTTCCTGACCTTGTGA TATTTTTAGTAGAGACGGGGTTTCACTGTGCTGGCCAGGATGGTCTCGATTTCCTGACCTTGTGA T C ARID4B,RBM34 Ensembl:ENSG00000054267,Ensembl:ENSG00000188739 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs947842966 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24658257 RMVar_hsa_circ_55137,RMVar_hsa_circ_111668,RMVar_hsa_circ_140672,RMVar_hsa_circ_304133,RMVar_hsa_circ_140675,RMVar_hsa_circ_287600,RMVar_hsa_circ_140676,RMVar_hsa_circ_295578,RMVar_hsa_circ_278108,RMVar_hsa_circ_140678,RMVar_hsa_circ_267527,RMVar_hsa_circ_140679 28179 RMVar_ID_28179 Human_SNP_ID_54259774 A-to-I Human chr1 - 235164498 235164498 235164498 TAGTCAGGATGGTCTCGATCTCCTGACCTCGTAATCTGCCCGCCTTGACCTCACAAAGTGTTGGG TAGTCAGGATGGTCTCGATCTCCTGACCTCGTGATCTGCCCGCCTTGACCTCACAAAGTGTTGGG T C ARID4B Ensembl:ENSG00000054267 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1188569075 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111668,RMVar_hsa_circ_140672 28180 RMVar_ID_28180 Human_SNP_ID_54261913 A-to-I Human chr1 - 235172422 235172422 235172422 AGGCATGCACCACCAAGCCCGGCTAATTTTGTATTTTTTAGGTAGAGACAGGGTTTCGCCATGTC AGGCATGCACCACCAAGCCCGGCTAATTTTGTGTTTTTTAGGTAGAGACAGGGTTTCGCCATGTC T C ARID4B Ensembl:ENSG00000054267 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1478462631 Functional Loss SNV dbSNP153 33..33 33 - - - 28181 RMVar_ID_28181 Human_SNP_ID_54269391 A-to-I Human chr1 - 235200127 235200127 235200127 TTTGTTAGAGACGGAGTTTCACCACGTTGGCCAGGCTGGTCTCGAACTCCTGGCCTCGGGTGATC TTTGTTAGAGACGGAGTTTCACCACGTTGGCCGGGCTGGTCTCGAACTCCTGGCCTCGGGTGATC T C ARID4B Ensembl:ENSG00000054267 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1383691731 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10850590 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_74498,RMVar_hsa_circ_140689,RMVar_hsa_circ_355731 28182 RMVar_ID_28182 Human_SNP_ID_54269885 A-to-I Human chr1 - 235201846 235201846 235201846 AGAGTCTTGCTCTGTTTCCCAGGTTGGAGTGCAGTAGTGCAGTCTTGGCTCACTGCAACCTCTGC AGAGTCTTGCTCTGTTTCCCAGGTTGGAGTGCCGTAGTGCAGTCTTGGCTCACTGCAACCTCTGC T G ARID4B Ensembl:ENSG00000054267 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1403378467 Functional Loss SNV dbSNP153 33..33 33 - - - 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_74498,RMVar_hsa_circ_140689,RMVar_hsa_circ_355731 28183 RMVar_ID_28183 Human_SNP_ID_54272371 A-to-I Human chr1 - 235211641 235211641 235211641 CCAGGAATTCGAGGCTGCAGTGAACTATGATCATGCCACTGTACTCCAGCCTGAGTGCCAGAATG CCAGGAATTCGAGGCTGCAGTGAACTATGATCGTGCCACTGTACTCCAGCCTGAGTGCCAGAATG T C ARID4B Ensembl:ENSG00000054267 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs972550802 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2133863,Human_RBP_ID_10850826,Human_RBP_ID_24658739 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_74498,RMVar_hsa_circ_140689,RMVar_hsa_circ_355731 28184 RMVar_ID_28184 Human_SNP_ID_54277818 A-to-I Human chr1 - 235231554 235231554 235231554 TGAGCCTGGGAGGTAGAGGTTGTGGTGAGCCAAGATTGTGCCACTGCACTCCAGTCTGGATGACA TGAGCCTGGGAGGTAGAGGTTGTGGTGAGCCAGGATTGTGCCACTGCACTCCAGTCTGGATGACA T C ARID4B Ensembl:ENSG00000054267 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs950053794 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4746,RMVar_hsa_circ_108942,RMVar_hsa_circ_66367,RMVar_hsa_circ_109816,RMVar_hsa_circ_40130,RMVar_hsa_circ_140680,RMVar_hsa_circ_140687,RMVar_hsa_circ_368977,RMVar_hsa_circ_306475,RMVar_hsa_circ_285230,RMVar_hsa_circ_140691,RMVar_hsa_circ_140692,RMVar_hsa_circ_333461,RMVar_hsa_circ_366396,RMVar_hsa_circ_321483,RMVar_hsa_circ_75348,RMVar_hsa_circ_140698,RMVar_hsa_circ_6081,RMVar_hsa_circ_140694,RMVar_hsa_circ_54508,RMVar_hsa_circ_21959,RMVar_hsa_circ_5878,RMVar_hsa_circ_363550,RMVar_hsa_circ_365969,RMVar_hsa_circ_334710,RMVar_hsa_circ_67344,RMVar_hsa_circ_274930,RMVar_hsa_circ_140699,RMVar_hsa_circ_54614 28185 RMVar_ID_28185 Human_SNP_ID_54277837 A-to-I Human chr1 - 235231624 235231624 235231624 AATTAGCCGGGTGGTAGTGGCATGTGCCTGTAATCCCAGCTACTCGGGAGGTTGAGGCAGAAGAA AATTAGCCGGGTGGTAGTGGCATGTGCCTGTAGTCCCAGCTACTCGGGAGGTTGAGGCAGAAGAA T C ARID4B Ensembl:ENSG00000054267 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1031162121 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4746,RMVar_hsa_circ_108942,RMVar_hsa_circ_66367,RMVar_hsa_circ_109816,RMVar_hsa_circ_40130,RMVar_hsa_circ_140680,RMVar_hsa_circ_140687,RMVar_hsa_circ_368977,RMVar_hsa_circ_306475,RMVar_hsa_circ_285230,RMVar_hsa_circ_140691,RMVar_hsa_circ_140692,RMVar_hsa_circ_333461,RMVar_hsa_circ_366396,RMVar_hsa_circ_321483,RMVar_hsa_circ_75348,RMVar_hsa_circ_140698,RMVar_hsa_circ_6081,RMVar_hsa_circ_140694,RMVar_hsa_circ_54508,RMVar_hsa_circ_21959,RMVar_hsa_circ_5878,RMVar_hsa_circ_363550,RMVar_hsa_circ_365969,RMVar_hsa_circ_334710,RMVar_hsa_circ_67344,RMVar_hsa_circ_274930,RMVar_hsa_circ_140699,RMVar_hsa_circ_54614 28186 RMVar_ID_28186 Human_SNP_ID_54277869 A-to-I Human chr1 - 235231763 235231763 235231763 TCGTTTTTGGCCGGGTGTGGTGGCTCATGCCTATAATCCCAGTACTTTGGGAGACTGAGGTGGGT TCGTTTTTGGCCGGGTGTGGTGGCTCATGCCTGTAATCCCAGTACTTTGGGAGACTGAGGTGGGT T C ARID4B Ensembl:ENSG00000054267 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs923378976 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4746,RMVar_hsa_circ_108942,RMVar_hsa_circ_66367,RMVar_hsa_circ_109816,RMVar_hsa_circ_40130,RMVar_hsa_circ_140680,RMVar_hsa_circ_140687,RMVar_hsa_circ_368977,RMVar_hsa_circ_306475,RMVar_hsa_circ_285230,RMVar_hsa_circ_140691,RMVar_hsa_circ_140692,RMVar_hsa_circ_333461,RMVar_hsa_circ_366396,RMVar_hsa_circ_321483,RMVar_hsa_circ_75348,RMVar_hsa_circ_140698,RMVar_hsa_circ_6081,RMVar_hsa_circ_140694,RMVar_hsa_circ_54508,RMVar_hsa_circ_21959,RMVar_hsa_circ_5878,RMVar_hsa_circ_363550,RMVar_hsa_circ_365969,RMVar_hsa_circ_334710,RMVar_hsa_circ_67344,RMVar_hsa_circ_274930,RMVar_hsa_circ_140699,RMVar_hsa_circ_54614 28187 RMVar_ID_28187 Human_SNP_ID_54290034 A-to-I Human chr1 - 235277785 235277785 235277785 CTTATGGTCCTAAGTGAATAGTTGGAATAGATATCCTCAGCAACTAATAGAATCTCCATTTAGTG CTTATGGTCCTAAGTGAATAGTTGGAATAGATGTCCTCAGCAACTAATAGAATCTCCATTTAGTG T C ARID4B Ensembl:ENSG00000054267 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs376230141 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10852169 28188 RMVar_ID_28188 Human_SNP_ID_54294671 A-to-I Human chr1 - 235296733 235296722 235296733 AATTATGGCTGGGTGAGGTGGCTCACTCCTGTAACCTAAGCACTCTGGGAGGCTGAGGTGGGCGG AATTATGGCTGGGTGAGGTGGCTCACTCCTGT___________TCTGGGAGGCTGAGGTGGGCGG AGTGCTTAGGTT A ARID4B Ensembl:ENSG00000054267 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1303658336 Functional Loss DEL dbSNP153 33..43 33 - - - 28189 RMVar_ID_28189 Human_SNP_ID_54295377 A-to-I Human chr1 - 235299036 235299036 235299036 TTGTCTAGGCTGGCTTGGAACTCCTGGGTTCAAGCCATCCTCTTGCCTCTGCCTCCCGAGTAGCT TTGTCTAGGCTGGCTTGGAACTCCTGGGTTCAGGCCATCCTCTTGCCTCTGCCTCCCGAGTAGCT T C ARID4B Ensembl:ENSG00000054267 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1248377003 Functional Loss SNV dbSNP153 33..33 33 - - - 28190 RMVar_ID_28190 Human_SNP_ID_54300052 A-to-I Human chr1 - 235315322 235315322 235315322 GGGCTCAAGTGATCTTCCTACCTCAGTCACCCAAGTAGCTGAGACTACAAATAATGCACACCACC GGGCTCAAGTGATCTTCCTACCTCAGTCACCCCAGTAGCTGAGACTACAAATAATGCACACCACC T G ARID4B Ensembl:ENSG00000054267 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1339429292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10853025 28191 RMVar_ID_28191 Human_SNP_ID_54302099 A-to-I Human chr1 - 235323202 235323202 235323202 AACCCCGTCTCTACTAAAAGTATAAAAAAATTAGCTGGGCATGGTGGCGCATGCCTGTATTCCCA AACCCCGTCTCTACTAAAAGTATAAAAAAATTGGCTGGGCATGGTGGCGCATGCCTGTATTCCCA T C ARID4B Ensembl:ENSG00000054267 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1164264964 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10853318 28192 RMVar_ID_28192 Human_SNP_ID_54330153 A-to-I Human chr1 + 235426677 235426673 235426677 TTAATTTATTTTTAGTTTTTTGAGACAGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGCGCA TTAATTTATTTTTAGTTTTTTGAGACAGT____CTCTGTCACCCAGGCTGGAGTGCAGTGGCGCA TCTCA T TBCE,TBCE:2 Ensembl:ENSG00000284770,Ensembl:ENSG00000285053 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1266005301 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_267894,RMVar_hsa_circ_50620,RMVar_hsa_circ_140716,RMVar_hsa_circ_25310,RMVar_hsa_circ_21744,RMVar_hsa_circ_337248,RMVar_hsa_circ_340405,RMVar_hsa_circ_314843,RMVar_hsa_circ_58291,RMVar_hsa_circ_70967,RMVar_hsa_circ_331478,RMVar_hsa_circ_345347,RMVar_hsa_circ_140713,RMVar_hsa_circ_339013,RMVar_hsa_circ_299005,RMVar_hsa_circ_39819,RMVar_hsa_circ_15289,RMVar_hsa_circ_292972,RMVar_hsa_circ_140714,RMVar_hsa_circ_140715,RMVar_hsa_circ_319435,RMVar_hsa_circ_350466,RMVar_hsa_circ_317266,RMVar_hsa_circ_274188,RMVar_hsa_circ_281680,RMVar_hsa_circ_29401,RMVar_hsa_circ_140718,RMVar_hsa_circ_140720,RMVar_hsa_circ_140721,RMVar_hsa_circ_140719,RMVar_hsa_circ_140717 28193 RMVar_ID_28193 Human_SNP_ID_54332230 A-to-I Human chr1 + 235434562 235434562 235434562 GTTTCTTTTTTTTCTTTTTCTTTTTTTGAGACAGAGTCTCACTCTGTCGCCCAGGCTGGAGTGCA GTTTCTTTTTTTTCTTTTTCTTTTTTTGAGACGGAGTCTCACTCTGTCGCCCAGGCTGGAGTGCA A G TBCE,TBCE:2 Ensembl:ENSG00000284770,Ensembl:ENSG00000285053 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs887035285 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267894,RMVar_hsa_circ_25310,RMVar_hsa_circ_21744,RMVar_hsa_circ_314843,RMVar_hsa_circ_58291,RMVar_hsa_circ_70967,RMVar_hsa_circ_331478,RMVar_hsa_circ_39819,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_140726,RMVar_hsa_circ_11762,RMVar_hsa_circ_69609,RMVar_hsa_circ_342463,RMVar_hsa_circ_357469,RMVar_hsa_circ_342105,RMVar_hsa_circ_73946,RMVar_hsa_circ_140724,RMVar_hsa_circ_321393,RMVar_hsa_circ_11683,RMVar_hsa_circ_288563,RMVar_hsa_circ_336145,RMVar_hsa_circ_279972,RMVar_hsa_circ_140727,RMVar_hsa_circ_140728 28194 RMVar_ID_28194 Human_SNP_ID_54335378 A-to-I Human chr1 + 235445365 235445365 235445365 AACAGAAAAGTAATAGCCAGGCATGGTGGCTCACACCTGTAATCCTAGCACTTTGGGAGGCCAAG AACAGAAAAGTAATAGCCAGGCATGGTGGCTCGCACCTGTAATCCTAGCACTTTGGGAGGCCAAG A G TBCE,TBCE:2 Ensembl:ENSG00000284770,Ensembl:ENSG00000285053 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1455272293 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29401,RMVar_hsa_circ_11683,RMVar_hsa_circ_140732,RMVar_hsa_circ_324615,RMVar_hsa_circ_140731,RMVar_hsa_circ_351592,RMVar_hsa_circ_51362 28195 RMVar_ID_28195 Human_SNP_ID_54343112 A-to-I Human chr1 - 235474813 235474813 235474813 TAGCATTATGGACGCTTACATCCTTAGACAGAATTTCACTCCTGTTGCCCAGGCTGGAGTGCAAT TAGCATTATGGACGCTTACATCCTTAGACAGAGTTTCACTCCTGTTGCCCAGGCTGGAGTGCAAT T C B3GALNT2 Ensembl:ENSG00000162885 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1214121559 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2742,RMVar_hsa_circ_352347,RMVar_hsa_circ_282932,RMVar_hsa_circ_357673,RMVar_hsa_circ_305534,RMVar_hsa_circ_302189,RMVar_hsa_circ_27570,RMVar_hsa_circ_7916,RMVar_hsa_circ_58422,RMVar_hsa_circ_297446,RMVar_hsa_circ_312925,RMVar_hsa_circ_271849,RMVar_hsa_circ_270881,RMVar_hsa_circ_300980 28196 RMVar_ID_28196 Human_SNP_ID_54344232 A-to-I Human chr1 - 235478315 235478315 235478315 CGGGCTCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGTGGATCACAAGG CGGGCTCAGTGGCTCACACCTGTAATCCCAGCCCTTTGGGAGGCCAAGGCGGGTGGATCACAAGG T G B3GALNT2 Ensembl:ENSG00000162885 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1304044347 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2742,RMVar_hsa_circ_352347,RMVar_hsa_circ_282932,RMVar_hsa_circ_357673,RMVar_hsa_circ_305534,RMVar_hsa_circ_302189,RMVar_hsa_circ_27570,RMVar_hsa_circ_7916,RMVar_hsa_circ_58422,RMVar_hsa_circ_297446,RMVar_hsa_circ_312925,RMVar_hsa_circ_271849,RMVar_hsa_circ_270881,RMVar_hsa_circ_300980 28197 RMVar_ID_28197 Human_SNP_ID_54344235 A-to-I Human chr1 - 235478323 235478323 235478323 GTTCAGGTCGGGCTCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGTGGA GTTCAGGTCGGGCTCAGTGGCTCACACCTGTAGTCCCAGCACTTTGGGAGGCCAAGGCGGGTGGA T C B3GALNT2 Ensembl:ENSG00000162885 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1158237699 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2742,RMVar_hsa_circ_352347,RMVar_hsa_circ_282932,RMVar_hsa_circ_357673,RMVar_hsa_circ_305534,RMVar_hsa_circ_302189,RMVar_hsa_circ_27570,RMVar_hsa_circ_7916,RMVar_hsa_circ_58422,RMVar_hsa_circ_297446,RMVar_hsa_circ_312925,RMVar_hsa_circ_271849,RMVar_hsa_circ_270881,RMVar_hsa_circ_300980 28198 RMVar_ID_28198 Human_SNP_ID_54346156 A-to-I Human chr1 - 235486004 235486004 235486004 TCACTGCAGCCTCTTCCTCCCAGGCTCAAGCAATTCTCGTGCCTCAGCCTCCCAAGTAGGTGGGA TCACTGCAGCCTCTTCCTCCCAGGCTCAAGCAGTTCTCGTGCCTCAGCCTCCCAAGTAGGTGGGA T C B3GALNT2 Ensembl:ENSG00000162885 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs763575059 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_352347,RMVar_hsa_circ_357673,RMVar_hsa_circ_27570,RMVar_hsa_circ_297446,RMVar_hsa_circ_312925,RMVar_hsa_circ_270881,RMVar_hsa_circ_281456,RMVar_hsa_circ_288386,RMVar_hsa_circ_320504 28199 RMVar_ID_28199 Human_SNP_ID_54392546 A-to-I Human chr1 - 235664918 235664918 235664918 GTGGTGGCGTGCACCTGTTGTCCCAGCAACTTAGAAGGCTGAGGCAGAAGAATCTCTTGAATTCA GTGGTGGCGTGCACCTGTTGTCCCAGCAACTTGGAAGGCTGAGGCAGAAGAATCTCTTGAATTCA T C LYST Ensembl:ENSG00000143669 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1360614526 Functional Loss SNV dbSNP153 33..33 33 - - - 28200 RMVar_ID_28200 Human_SNP_ID_54411676 A-to-I Human chr1 - 235750153 235750153 235750153 GTAGAAACAGATTCTTTATCAGTTCTAGCATTAGTGCTCAGCTTCCTGCATGCCAAAACATGATT GTAGAAACAGATTCTTTATCAGTTCTAGCATTGGTGCTCAGCTTCCTGCATGCCAAAACATGATT T C LYST Ensembl:ENSG00000143669 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs550617542 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15432,RMVar_hsa_circ_352206,RMVar_hsa_circ_4398,RMVar_hsa_circ_73903,RMVar_hsa_circ_72057,RMVar_hsa_circ_90554,RMVar_hsa_circ_140751,RMVar_hsa_circ_267360,RMVar_hsa_circ_89370,RMVar_hsa_circ_58840,RMVar_hsa_circ_140753,RMVar_hsa_circ_53886,RMVar_hsa_circ_348969,RMVar_hsa_circ_336182,RMVar_hsa_circ_363137,RMVar_hsa_circ_26167,RMVar_hsa_circ_35707,RMVar_hsa_circ_18617,RMVar_hsa_circ_25998,RMVar_hsa_circ_112826,RMVar_hsa_circ_140754 28201 RMVar_ID_28201 Human_SNP_ID_54411678 A-to-I Human chr1 - 235750159 235750159 235750159 TCCTGAGTAGAAACAGATTCTTTATCAGTTCTAGCATTAGTGCTCAGCTTCCTGCATGCCAAAAC TCCTGAGTAGAAACAGATTCTTTATCAGTTCTGGCATTAGTGCTCAGCTTCCTGCATGCCAAAAC T C LYST Ensembl:ENSG00000143669 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1269299595 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15432,RMVar_hsa_circ_352206,RMVar_hsa_circ_4398,RMVar_hsa_circ_73903,RMVar_hsa_circ_72057,RMVar_hsa_circ_90554,RMVar_hsa_circ_140751,RMVar_hsa_circ_267360,RMVar_hsa_circ_89370,RMVar_hsa_circ_58840,RMVar_hsa_circ_140753,RMVar_hsa_circ_53886,RMVar_hsa_circ_348969,RMVar_hsa_circ_336182,RMVar_hsa_circ_363137,RMVar_hsa_circ_26167,RMVar_hsa_circ_35707,RMVar_hsa_circ_18617,RMVar_hsa_circ_25998,RMVar_hsa_circ_112826,RMVar_hsa_circ_140754 28202 RMVar_ID_28202 Human_SNP_ID_54428674 A-to-I Human chr1 - 235821350 235821350 235821350 CCTCTGCAACCTCTGCCTCCCAGGCGCAAGCAATCCTCCCACCTCAGCCTCCCAAATAGCTGTGA CCTCTGCAACCTCTGCCTCCCAGGCGCAAGCAGTCCTCCCACCTCAGCCTCCCAAATAGCTGTGA T C LYST Ensembl:ENSG00000143669 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs570639590 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_352206,RMVar_hsa_circ_72057,RMVar_hsa_circ_18617,RMVar_hsa_circ_14527,RMVar_hsa_circ_347117,RMVar_hsa_circ_140781,RMVar_hsa_circ_351682 28203 RMVar_ID_28203 Human_SNP_ID_54437569 A-to-I Human chr1 - 235861767 235861767 235861767 GTCTCCGAAGCCAGGAGCCATGGCTTGTGCCTATAGTCCCAGTTACTTGGAAGACTGAGGTGGGA GTCTCCGAAGCCAGGAGCCATGGCTTGTGCCTGTAGTCCCAGTTACTTGGAAGACTGAGGTGGGA T C LYST Ensembl:ENSG00000143669 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1201431208 Functional Loss SNV dbSNP153 33..33 33 - - - 28204 RMVar_ID_28204 Human_SNP_ID_54437755 A-to-I Human chr1 - 235862579 235862579 235862579 GTTGCCCAGGCTGGTCTCGAACTGCTGACCTCAAGTGATCTGCCCATCTTGGCCTCCCAAAGTGC GTTGCCCAGGCTGGTCTCGAACTGCTGACCTCGAGTGATCTGCCCATCTTGGCCTCCCAAAGTGC T C LYST Ensembl:ENSG00000143669 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs931721009 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10856882 28205 RMVar_ID_28205 Human_SNP_ID_54541100 A-to-I Human chr1 - 236264381 236264381 236264381 AAGTTGTCTGGGCATGGTGGCTTCTGCCTGTAATCCCGGCACGCTGGGAGGCTGAGGCAAGTGGA AAGTTGTCTGGGCATGGTGGCTTCTGCCTGTAGTCCCGGCACGCTGGGAGGCTGAGGCAAGTGGA T C ERO1B Ensembl:ENSG00000086619 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1413995281 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_308315,RMVar_hsa_circ_140829,RMVar_hsa_circ_349732 28206 RMVar_ID_28206 Human_SNP_ID_54542074 A-to-I Human chr1 - 236268412 236268412 236268412 TTTTTTAGACAGGGTCTCGCTCTGTCGCCCAGACTGGAGTGCAGTGGCTCCATCTCAGTTCACTG TTTTTTAGACAGGGTCTCGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCTCCATCTCAGTTCACTG T C ERO1B Ensembl:ENSG00000086619 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1254440426 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_308315,RMVar_hsa_circ_140829,RMVar_hsa_circ_349732,RMVar_hsa_circ_140830 28207 RMVar_ID_28207 Human_SNP_ID_54543598 A-to-I Human chr1 - 236274263 236274263 236274263 TGATGAGGATATGGGCTGGCACAGTGGCTCACACCTGCAATCCCAGCACTTTGAGAGGCTGAGGC TGATGAGGATATGGGCTGGCACAGTGGCTCACGCCTGCAATCCCAGCACTTTGAGAGGCTGAGGC T C ERO1B Ensembl:ENSG00000086619 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1046164191 Functional Loss SNV dbSNP153 33..33 33 - - - 28208 RMVar_ID_28208 Human_SNP_ID_54615588 A-to-I Human chr1 - 236552033 236552033 236552033 AAACTAAAGGAGAATTATATTGTCTTGCTACCAGAATCCATTCCTTTCTTAGCAGAGTTGATGGA AAACTAAAGGAGAATTATATTGTCTTGCTACCGGAATCCATTCCTTTCTTAGCAGAGTTGATGGA T C HEATR1 Ensembl:ENSG00000119285 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs755234337 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1741672,Human_RBP_ID_5332387,Human_RBP_ID_17764503,Human_RBP_ID_18226982 Human_Splice_Rec_203338,Human_Splice_Rec_203339,Human_Splice_Rec_203424,Human_Splice_Rec_203425 RMVar_hsa_circ_109794,RMVar_hsa_circ_123102,RMVar_hsa_circ_119846,RMVar_hsa_circ_140841,RMVar_hsa_circ_140842,RMVar_hsa_circ_140840 28209 RMVar_ID_28209 Human_SNP_ID_54708657 A-to-I Human chr1 + 236912595 236912595 236912595 CTGGAGTGCAGTGGCGCGATCTTGGCTCACTGAAAGCTCTGCCTCCCGAGTTCACACCATTCTCC CTGGAGTGCAGTGGCGCGATCTTGGCTCACTGCAAGCTCTGCCTCCCGAGTTCACACCATTCTCC A C MTR Ensembl:ENSG00000116984 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1314971323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10864423 RMVar_hsa_circ_140927 28210 RMVar_ID_28210 Human_SNP_ID_54725639 A-to-I Human chr1 + 236981365 236981365 236981365 AGCAATGGCCAAGATCAAAGCTCGAGATCTTCACGGGAAGAAGAAGGAGGAGCTGCGGAAACAGC AGCAATGGCCAAGATCAAAGCTCGAGATCTTCGCGGGAAGAAGAAGGAGGAGCTGCGGAAACAGC A G RPL35P1 Ensembl:ENSG00000237991 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878989383 Functional Loss SNV dbSNP153 33..33 33 - - - 28211 RMVar_ID_28211 Human_SNP_ID_54755526 A-to-I Human chr1 + 237103803 237103802 237103804 GTTGGCCAGGCTGGTCTCGAACTCCTGACTTCAGGTGGTCCACCCGCCTCGGCCTCCCAAAGTGT GTTGGCCAGGCTGGTCTCGAACTCCTGACTTC__GTGGTCCACCCGCCTCGGCCTCCCAAAGTGT CAG C RYR2 Ensembl:ENSG00000198626 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs553014724 Functional Loss DEL dbSNP153 33..34 33 - - - 28212 RMVar_ID_28212 Human_SNP_ID_54814827 A-to-I Human chr1 + 237342248 237342248 237342248 ATAGCTCTCTGCAGCCTCCAATGCTGGGTCTCAAGGGATCTTCCTGCCTCCTGAGTAGCCAGGAC ATAGCTCTCTGCAGCCTCCAATGCTGGGTCTCCAGGGATCTTCCTGCCTCCTGAGTAGCCAGGAC A C RYR2 Ensembl:ENSG00000198626 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1273105372 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_46916,RMVar_hsa_circ_96860,RMVar_hsa_circ_1211,RMVar_hsa_circ_31733,RMVar_hsa_circ_140932 28213 RMVar_ID_28213 Human_SNP_ID_54814890 A-to-I Human chr1 + 237342414 237342402 237342415 GACCTTAAGTGATCCTCCCACCTTAACCTCCCAAAATGTTGGGATTACAGGTGTGAGCCACCTCA GACCTTAAGTGATCCTCCCAC_____________AATGTTGGGATTACAGGTGTGAGCCACCTCA CCTTAACCTCCCAA C RYR2 Ensembl:ENSG00000198626 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1403379562 Functional Loss DEL dbSNP153 22..34 33 - - - RMVar_hsa_circ_46916,RMVar_hsa_circ_96860,RMVar_hsa_circ_1211,RMVar_hsa_circ_31733,RMVar_hsa_circ_140932 28214 RMVar_ID_28214 Human_SNP_ID_54853560 A-to-I Human chr1 + 237496387 237496387 237496387 CTATGATTGCACTACTGCGCTTCAGCCTAGGCAACAGAGCAAGACTCTGTCTCAATAAAATTAAA CTATGATTGCACTACTGCGCTTCAGCCTAGGCGACAGAGCAAGACTCTGTCTCAATAAAATTAAA A G RYR2 Ensembl:ENSG00000198626 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1003890876 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_274,RMVar_hsa_circ_986,RMVar_hsa_circ_336938,RMVar_hsa_circ_354501,RMVar_hsa_circ_349399,RMVar_hsa_circ_322929,RMVar_hsa_circ_304178,RMVar_hsa_circ_107018,RMVar_hsa_circ_140939,RMVar_hsa_circ_33727,RMVar_hsa_circ_81557,RMVar_hsa_circ_140940,RMVar_hsa_circ_104095,RMVar_hsa_circ_332200,RMVar_hsa_circ_118098,RMVar_hsa_circ_8904,RMVar_hsa_circ_28916,RMVar_hsa_circ_83732,RMVar_hsa_circ_140953,RMVar_hsa_circ_140954,RMVar_hsa_circ_113557,RMVar_hsa_circ_140956,RMVar_hsa_circ_68295,RMVar_hsa_circ_140955,RMVar_hsa_circ_62240,RMVar_hsa_circ_4786,RMVar_hsa_circ_23140,RMVar_hsa_circ_43252,RMVar_hsa_circ_19696,RMVar_hsa_circ_42108,RMVar_hsa_circ_4415,RMVar_hsa_circ_140964,RMVar_hsa_circ_36019 28215 RMVar_ID_28215 Human_SNP_ID_55276131 A-to-I Human chr1 + 239177564 239177564 239177564 AACGCCGTCTCTACTAAAAATACAAAAAAATTAGCCGGGCGTGGTGGCGGGCGCCTGTGGTCCCG AACGCCGTCTCTACTAAAAATACAAAAAAATTGGCCGGGCGTGGTGGCGGGCGCCTGTGGTCCCG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1026691007 Functional Loss SNV dbSNP153 33..33 33 - - - 28216 RMVar_ID_28216 Human_SNP_ID_107809817 A-to-I Human chr2 + 195664973 195664973 195664973 GGGAAGCCGGGGTGGGAGGATTACTTAAGGCCAAGAGTTTGAGACCATCCTGGGCAACATAGGGA GGGAAGCCGGGGTGGGAGGATTACTTAAGGCCGAGAGTTTGAGACCATCCTGGGCAACATAGGGA A G SLC39A10 Ensembl:ENSG00000196950 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs915173853 Functional Loss SNV dbSNP153 33..33 33 - - - 28217 RMVar_ID_28217 Human_SNP_ID_107809848 A-to-I Human chr2 + 195665068 195665068 195665068 GTGTGAGGTCGGGCACGGTGGCTCACGCCTGTAATCCCAGCGCTTTGGGAGGCTGAGGGGGGCTG GTGTGAGGTCGGGCACGGTGGCTCACGCCTGTGATCCCAGCGCTTTGGGAGGCTGAGGGGGGCTG A G SLC39A10 Ensembl:ENSG00000196950 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs983504021 Functional Loss SNV dbSNP153 33..33 33 - - - 28218 RMVar_ID_28218 Human_SNP_ID_107810227 A-to-I Human chr2 + 195666722 195666722 195666722 GGGCTCAAGCCATATGCCTGCTTTGGTCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACTGCA GGGCTCAAGCCATATGCCTGCTTTGGTCTCCCGAAGTGCTGGGATTACAGGTGTGAGCCACTGCA A G SLC39A10 Ensembl:ENSG00000196950 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459207743 Functional Loss SNV dbSNP153 33..33 33 - - - 28219 RMVar_ID_28219 Human_SNP_ID_107929705 A-to-I Human chr2 - 196141547 196141547 196141547 TCAAGGGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCATGTGCCATCACACCTG TCAAGGGATTCTCCTGCCTCAGCCTCCTGAGTCGCTGGGATTACAGGCATGTGCCATCACACCTG T G STK17B Ensembl:ENSG00000081320 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs967481540 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101517,RMVar_hsa_circ_205498,RMVar_hsa_circ_76515,RMVar_hsa_circ_324363,RMVar_hsa_circ_205497,RMVar_hsa_circ_300675,RMVar_hsa_circ_75962,RMVar_hsa_circ_205500,RMVar_hsa_circ_352004,RMVar_hsa_circ_205501 28220 RMVar_ID_28220 Human_SNP_ID_107930914 A-to-I Human chr2 - 196146364 196146364 196146364 AAGTAGCTGAGATTATAGGCACCTGCCATCACACCCAGCTAATTTTTGTGTTTTTAGTAGAGATG AAGTAGCTGAGATTATAGGCACCTGCCATCACGCCCAGCTAATTTTTGTGTTTTTAGTAGAGATG T C STK17B Ensembl:ENSG00000081320 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs560488823 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_324363,RMVar_hsa_circ_72580 28221 RMVar_ID_28221 Human_SNP_ID_107930919 A-to-I Human chr2 - 196146382 196146382 196146382 CTCCTGCCTCAGCTTCCCAAGTAGCTGAGATTATAGGCACCTGCCATCACACCCAGCTAATTTTT CTCCTGCCTCAGCTTCCCAAGTAGCTGAGATTGTAGGCACCTGCCATCACACCCAGCTAATTTTT T C STK17B Ensembl:ENSG00000081320 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs544563600 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_324363,RMVar_hsa_circ_72580 28222 RMVar_ID_28222 Human_SNP_ID_107930934 A-to-I Human chr2 - 196146447 196146447 196146447 CAGGCTGGAATGCAGTGGTGCCATCTCGGCTCACTGCAACCTTTGCCTCCCAGGTTCAAGTGATT CAGGCTGGAATGCAGTGGTGCCATCTCGGCTCTCTGCAACCTTTGCCTCCCAGGTTCAAGTGATT T A STK17B Ensembl:ENSG00000081320 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1469488541 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_324363,RMVar_hsa_circ_72580 28223 RMVar_ID_28223 Human_SNP_ID_107930944 A-to-I Human chr2 - 196146470 196146470 196146470 GGACGGAGTCTTGCTCTGTAGCTCAGGCTGGAATGCAGTGGTGCCATCTCGGCTCACTGCAACCT GGACGGAGTCTTGCTCTGTAGCTCAGGCTGGAGTGCAGTGGTGCCATCTCGGCTCACTGCAACCT T C STK17B Ensembl:ENSG00000081320 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1482737455 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_324363,RMVar_hsa_circ_72580 28224 RMVar_ID_28224 Human_SNP_ID_107930946 A-to-I Human chr2 - 196146483 196146483 196146483 TTCTTTTTTTTGGGGACGGAGTCTTGCTCTGTAGCTCAGGCTGGAATGCAGTGGTGCCATCTCGG TTCTTTTTTTTGGGGACGGAGTCTTGCTCTGTGGCTCAGGCTGGAATGCAGTGGTGCCATCTCGG T C STK17B Ensembl:ENSG00000081320 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs995789241 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_324363,RMVar_hsa_circ_72580 28225 RMVar_ID_28225 Human_SNP_ID_107934009 A-to-I Human chr2 - 196158863 196158863 196158863 GGGATTACAGGCATGTGCCACCAAGCCCGGCTAATTTTTTGTATTTTTAGTAGAGACGGGATTTC GGGATTACAGGCATGTGCCACCAAGCCCGGCTTATTTTTTGTATTTTTAGTAGAGACGGGATTTC T A STK17B Ensembl:ENSG00000081320 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1042169924 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_324363,RMVar_hsa_circ_343275,RMVar_hsa_circ_205502 28226 RMVar_ID_28226 Human_SNP_ID_107934023 A-to-I Human chr2 - 196158928 196158928 196158928 CAGCTCACTGCAACCTCCGTCTGCCGAGTTCAAGTGATTCTCCTGCCTCAGCTTCCTGAGTAGCT CAGCTCACTGCAACCTCCGTCTGCCGAGTTCAGGTGATTCTCCTGCCTCAGCTTCCTGAGTAGCT T C STK17B Ensembl:ENSG00000081320 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs559241781 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_324363,RMVar_hsa_circ_343275,RMVar_hsa_circ_205502 28227 RMVar_ID_28227 Human_SNP_ID_107935007 A-to-I Human chr2 - 196162768 196162768 196162768 CTGCCACCTCAGCCTCCTAAGTAGCTGGGACTACAGGCACACACCACCACACTGGGCTGGTTTTT CTGCCACCTCAGCCTCCTAAGTAGCTGGGACTGCAGGCACACACCACCACACTGGGCTGGTTTTT T C STK17B Ensembl:ENSG00000081320 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1478567546 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_324363,RMVar_hsa_circ_343275,RMVar_hsa_circ_205502 28228 RMVar_ID_28228 Human_SNP_ID_107956627 A-to-I Human chr2 - 196255942 196255934 196255942 CAGCCTCCTGAGTAGCTGGGAGTACAGGTGCAAGCCACCACGCCCGGCTAATTTTTTGTATTTTA CAGCCTCCTGAGTAGCTGGGAGTACAGGTGCA________CGCCCGGCTAATTTTTTGTATTTTA GTGGTGGCT G HECW2 Ensembl:ENSG00000138411 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1457801074 Functional Loss DEL dbSNP153 33..40 33 - - - RMVar_hsa_circ_60092,RMVar_hsa_circ_350780,RMVar_hsa_circ_205504,RMVar_hsa_circ_377170,RMVar_hsa_circ_205503,RMVar_hsa_circ_34070,RMVar_hsa_circ_316873,RMVar_hsa_circ_119117,RMVar_hsa_circ_205507,RMVar_hsa_circ_205508,RMVar_hsa_circ_347161,RMVar_hsa_circ_301827,RMVar_hsa_circ_86913,RMVar_hsa_circ_52525,RMVar_hsa_circ_205510,RMVar_hsa_circ_54878,RMVar_hsa_circ_205511,RMVar_hsa_circ_205509,RMVar_hsa_circ_67130,RMVar_hsa_circ_315695,RMVar_hsa_circ_339075,RMVar_hsa_circ_205514,RMVar_hsa_circ_205515 28229 RMVar_ID_28229 Human_SNP_ID_107956631 A-to-I Human chr2 - 196255938 196255938 196255938 CTCCTGAGTAGCTGGGAGTACAGGTGCAAGCCACCACGCCCGGCTAATTTTTTGTATTTTAATAG CTCCTGAGTAGCTGGGAGTACAGGTGCAAGCCGCCACGCCCGGCTAATTTTTTGTATTTTAATAG T C HECW2 Ensembl:ENSG00000138411 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1387961636 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60092,RMVar_hsa_circ_350780,RMVar_hsa_circ_205504,RMVar_hsa_circ_377170,RMVar_hsa_circ_205503,RMVar_hsa_circ_34070,RMVar_hsa_circ_316873,RMVar_hsa_circ_119117,RMVar_hsa_circ_205507,RMVar_hsa_circ_205508,RMVar_hsa_circ_347161,RMVar_hsa_circ_301827,RMVar_hsa_circ_86913,RMVar_hsa_circ_52525,RMVar_hsa_circ_205510,RMVar_hsa_circ_54878,RMVar_hsa_circ_205511,RMVar_hsa_circ_205509,RMVar_hsa_circ_67130,RMVar_hsa_circ_315695,RMVar_hsa_circ_339075,RMVar_hsa_circ_205514,RMVar_hsa_circ_205515 28230 RMVar_ID_28230 Human_SNP_ID_107956634 A-to-I Human chr2 - 196255943 196255943 196255943 TCAGCCTCCTGAGTAGCTGGGAGTACAGGTGCAAGCCACCACGCCCGGCTAATTTTTTGTATTTT TCAGCCTCCTGAGTAGCTGGGAGTACAGGTGCGAGCCACCACGCCCGGCTAATTTTTTGTATTTT T C HECW2 Ensembl:ENSG00000138411 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs929445538 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60092,RMVar_hsa_circ_350780,RMVar_hsa_circ_205504,RMVar_hsa_circ_377170,RMVar_hsa_circ_205503,RMVar_hsa_circ_34070,RMVar_hsa_circ_316873,RMVar_hsa_circ_119117,RMVar_hsa_circ_205507,RMVar_hsa_circ_205508,RMVar_hsa_circ_347161,RMVar_hsa_circ_301827,RMVar_hsa_circ_86913,RMVar_hsa_circ_52525,RMVar_hsa_circ_205510,RMVar_hsa_circ_54878,RMVar_hsa_circ_205511,RMVar_hsa_circ_205509,RMVar_hsa_circ_67130,RMVar_hsa_circ_315695,RMVar_hsa_circ_339075,RMVar_hsa_circ_205514,RMVar_hsa_circ_205515 28231 RMVar_ID_28231 Human_SNP_ID_107978350 A-to-I Human chr2 - 196347355 196347355 196347355 ATTTTGTATTTTGAAAAATACAAAAATTAGCCAGGCGTGGTGGCTTACACCTGTAATCCTAGCAT ATTTTGTATTTTGAAAAATACAAAAATTAGCCGGGCGTGGTGGCTTACACCTGTAATCCTAGCAT T C HECW2 Ensembl:ENSG00000138411 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1010626565 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60092,RMVar_hsa_circ_355505,RMVar_hsa_circ_113053,RMVar_hsa_circ_205519,RMVar_hsa_circ_205520,RMVar_hsa_circ_74892,RMVar_hsa_circ_102072,RMVar_hsa_circ_267664,RMVar_hsa_circ_107501,RMVar_hsa_circ_288643,RMVar_hsa_circ_205534,RMVar_hsa_circ_205535,RMVar_hsa_circ_323517,RMVar_hsa_circ_367404 28232 RMVar_ID_28232 Human_SNP_ID_108029725 A-to-I Human chr2 - 196571609 196571609 196571609 GCAACCTCCGCTTCCCATGCCTTTCGTGCCTCAGCCTCCTGAGTAGGTGGGATTACAGGTAACTG GCAACCTCCGCTTCCCATGCCTTTCGTGCCTCGGCCTCCTGAGTAGGTGGGATTACAGGTAACTG T C HECW2 Ensembl:ENSG00000138411 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1249184079 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102072,RMVar_hsa_circ_205534 28233 RMVar_ID_28233 Human_SNP_ID_108102041 A-to-I Human chr2 - 196879159 196879159 196879159 TGAAGCAGGAGAATCATTTGAACCCAGGAGGTAGAGGTTGTAGTATGCTATGATTATGCCTGTGA TGAAGCAGGAGAATCATTTGAACCCAGGAGGTGGAGGTTGTAGTATGCTATGATTATGCCTGTGA T C PGAP1 Ensembl:ENSG00000197121 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1250421742 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13725797 RMVar_hsa_circ_118184,RMVar_hsa_circ_337271,RMVar_hsa_circ_205558,RMVar_hsa_circ_205559,RMVar_hsa_circ_12499,RMVar_hsa_circ_31032,RMVar_hsa_circ_205563,RMVar_hsa_circ_342338,RMVar_hsa_circ_111362,RMVar_hsa_circ_320362,RMVar_hsa_circ_344413,RMVar_hsa_circ_205564,RMVar_hsa_circ_328036,RMVar_hsa_circ_301546,RMVar_hsa_circ_46395,RMVar_hsa_circ_65391,RMVar_hsa_circ_20724,RMVar_hsa_circ_18400,RMVar_hsa_circ_205565,RMVar_hsa_circ_205566,RMVar_hsa_circ_205567,RMVar_hsa_circ_323718,RMVar_hsa_circ_335354,RMVar_hsa_circ_329403,RMVar_hsa_circ_51069,RMVar_hsa_circ_9896,RMVar_hsa_circ_35973,RMVar_hsa_circ_336253,RMVar_hsa_circ_205569,RMVar_hsa_circ_29818,RMVar_hsa_circ_364443,RMVar_hsa_circ_205572,RMVar_hsa_circ_36510,RMVar_hsa_circ_276606,RMVar_hsa_circ_285625,RMVar_hsa_circ_339176,RMVar_hsa_circ_50228,RMVar_hsa_circ_205573,RMVar_hsa_circ_205571 28234 RMVar_ID_28234 Human_SNP_ID_108188576 A-to-I Human chr2 - 197262707 197262707 197262707 TAGAGACAGGGTTTCACCATATTGGGCAGATTAGTCTTGAACTCCTGGCCTCAAGTGATCCACCC TAGAGACAGGGTTTCACCATATTGGGCAGATTCGTCTTGAACTCCTGGCCTCAAGTGATCCACCC T G ANKRD44-IT1,ANKRD44 Ensembl:ENSG00000236977,Ensembl:ENSG00000065413 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215062798 Functional Loss SNV dbSNP153 33..33 33 - - - 28235 RMVar_ID_28235 Human_SNP_ID_108191411 A-to-I Human chr2 - 197274980 197274980 197274980 CTCCTACCACAGCCTCCCAAGTAGCTGGGACTACAGGTGCATGCCACCACACCTGGCTAATTTTT CTCCTACCACAGCCTCCCAAGTAGCTGGGACTGCAGGTGCATGCCACCACACCTGGCTAATTTTT T C ANKRD44-IT1,ANKRD44 Ensembl:ENSG00000236977,Ensembl:ENSG00000065413 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs996417489 Functional Loss SNV dbSNP153 33..33 33 - - - 28236 RMVar_ID_28236 Human_SNP_ID_108219277 A-to-I Human chr2 - 197393581 197393581 197393581 AGGCGTGGTGGCACACACCTGTAATTCCAGCTACTCAGGAGGCTGAGGCAGGCGAATTGCTTGAA AGGCGTGGTGGCACACACCTGTAATTCCAGCTGCTCAGGAGGCTGAGGCAGGCGAATTGCTTGAA T C SF3B1 Ensembl:ENSG00000115524 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs896579006 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87864,RMVar_hsa_circ_101657,RMVar_hsa_circ_127043,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_77845,RMVar_hsa_circ_85385,RMVar_hsa_circ_75591,RMVar_hsa_circ_205645,RMVar_hsa_circ_205646,RMVar_hsa_circ_205644,RMVar_hsa_circ_205641,RMVar_hsa_circ_205642,RMVar_hsa_circ_205640,RMVar_hsa_circ_205637,RMVar_hsa_circ_205638,RMVar_hsa_circ_205636 28237 RMVar_ID_28237 Human_SNP_ID_108219603 A-to-I Human chr2 - 197394842 197394842 197394842 GGAGTGCAGTGGCATGATCTCGGCATACTGCAACCTCTGCCTCCCAGGTTCAAGTGATTCTTCTG GGAGTGCAGTGGCATGATCTCGGCATACTGCAGCCTCTGCCTCCCAGGTTCAAGTGATTCTTCTG T C SF3B1 Ensembl:ENSG00000115524 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1210828750 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13726251 RMVar_hsa_circ_87864,RMVar_hsa_circ_101657,RMVar_hsa_circ_127043,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_77845,RMVar_hsa_circ_85385,RMVar_hsa_circ_75591,RMVar_hsa_circ_205645,RMVar_hsa_circ_205646,RMVar_hsa_circ_205644,RMVar_hsa_circ_205641,RMVar_hsa_circ_205642,RMVar_hsa_circ_205640,RMVar_hsa_circ_205637,RMVar_hsa_circ_205638,RMVar_hsa_circ_205636 28238 RMVar_ID_28238 Human_SNP_ID_108219607 A-to-I Human chr2 - 197394861 197394861 197394861 TTGCTGTGTCACCCAGTCTGGAGTGCAGTGGCATGATCTCGGCATACTGCAACCTCTGCCTCCCA TTGCTGTGTCACCCAGTCTGGAGTGCAGTGGCGTGATCTCGGCATACTGCAACCTCTGCCTCCCA T C SF3B1 Ensembl:ENSG00000115524 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs776474213 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87864,RMVar_hsa_circ_101657,RMVar_hsa_circ_127043,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_77845,RMVar_hsa_circ_85385,RMVar_hsa_circ_75591,RMVar_hsa_circ_205645,RMVar_hsa_circ_205646,RMVar_hsa_circ_205644,RMVar_hsa_circ_205641,RMVar_hsa_circ_205642,RMVar_hsa_circ_205640,RMVar_hsa_circ_205637,RMVar_hsa_circ_205638,RMVar_hsa_circ_205636 28239 RMVar_ID_28239 Human_SNP_ID_108223716 A-to-I Human chr2 - 197411625 197411625 197411625 CTCTGTCGCTCAGCCTGGAGTGCAGTGGTGCTATCTCGGCTCACTGCAAACTCTGCCTCCCGGGT CTCTGTCGCTCAGCCTGGAGTGCAGTGGTGCTGTCTCGGCTCACTGCAAACTCTGCCTCCCGGGT T C SF3B1 Ensembl:ENSG00000115524 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991586571 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10010,RMVar_hsa_circ_120089,RMVar_hsa_circ_205649,RMVar_hsa_circ_79158,RMVar_hsa_circ_205656,RMVar_hsa_circ_205657,RMVar_hsa_circ_98855,RMVar_hsa_circ_112496,RMVar_hsa_circ_205659,RMVar_hsa_circ_113648,RMVar_hsa_circ_357883,RMVar_hsa_circ_205663,RMVar_hsa_circ_205662,RMVar_hsa_circ_205664,RMVar_hsa_circ_205665,RMVar_hsa_circ_74879,RMVar_hsa_circ_116708,RMVar_hsa_circ_365688 28240 RMVar_ID_28240 Human_SNP_ID_108224043 A-to-I Human chr2 - 197412728 197412728 197412728 CACCCGCCTTGGCCTCCCAAGGTGCTGGGATTACACGTGTGAGCCACTGCGCCTGGCATGAGAGC CACCCGCCTTGGCCTCCCAAGGTGCTGGGATTCCACGTGTGAGCCACTGCGCCTGGCATGAGAGC T G SF3B1 Ensembl:ENSG00000115524 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1402203354 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17570102,Human_RBP_ID_25496405 RMVar_hsa_circ_10010,RMVar_hsa_circ_120089,RMVar_hsa_circ_205649,RMVar_hsa_circ_79158,RMVar_hsa_circ_205656,RMVar_hsa_circ_205657,RMVar_hsa_circ_98855,RMVar_hsa_circ_112496,RMVar_hsa_circ_205659,RMVar_hsa_circ_113648,RMVar_hsa_circ_357883,RMVar_hsa_circ_205663,RMVar_hsa_circ_205662,RMVar_hsa_circ_205664,RMVar_hsa_circ_205665,RMVar_hsa_circ_74879,RMVar_hsa_circ_116708,RMVar_hsa_circ_365688 28241 RMVar_ID_28241 Human_SNP_ID_108224207 A-to-I Human chr2 - 197413289 197413289 197413289 TCAAGTGACTCTTGTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCATGTGCCATCACGCCCA TCAAGTGACTCTTGTGCCTCAGCCTCCCAAGTGGCTGGGATTACAGGCATGTGCCATCACGCCCA T C SF3B1 Ensembl:ENSG00000115524 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1240639458 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10010,RMVar_hsa_circ_120089,RMVar_hsa_circ_205649,RMVar_hsa_circ_79158,RMVar_hsa_circ_205656,RMVar_hsa_circ_205657,RMVar_hsa_circ_98855,RMVar_hsa_circ_112496,RMVar_hsa_circ_205659,RMVar_hsa_circ_113648,RMVar_hsa_circ_357883,RMVar_hsa_circ_205663,RMVar_hsa_circ_205662,RMVar_hsa_circ_205664,RMVar_hsa_circ_205665,RMVar_hsa_circ_74879,RMVar_hsa_circ_116708,RMVar_hsa_circ_365688 28242 RMVar_ID_28242 Human_SNP_ID_108224208 A-to-I Human chr2 - 197413289 197413289 197413289 TCAAGTGACTCTTGTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCATGTGCCATCACGCCCA TCAAGTGACTCTTGTGCCTCAGCCTCCCAAGTCGCTGGGATTACAGGCATGTGCCATCACGCCCA T G SF3B1 Ensembl:ENSG00000115524 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1240639458 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10010,RMVar_hsa_circ_120089,RMVar_hsa_circ_205649,RMVar_hsa_circ_79158,RMVar_hsa_circ_205656,RMVar_hsa_circ_205657,RMVar_hsa_circ_98855,RMVar_hsa_circ_112496,RMVar_hsa_circ_205659,RMVar_hsa_circ_113648,RMVar_hsa_circ_357883,RMVar_hsa_circ_205663,RMVar_hsa_circ_205662,RMVar_hsa_circ_205664,RMVar_hsa_circ_205665,RMVar_hsa_circ_74879,RMVar_hsa_circ_116708,RMVar_hsa_circ_365688 28243 RMVar_ID_28243 Human_SNP_ID_108224375 A-to-I Human chr2 - 197413912 197413911 197413912 ATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCACTTGAACCCGGGAGGTGGAGGTTGCAGTG ATCCCAGCTACTTGGGAGGCTGAGGCAGGAGA_TCACTTGAACCCGGGAGGTGGAGGTTGCAGTG AT A SF3B1 Ensembl:ENSG00000115524 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1455139984 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_10010,RMVar_hsa_circ_120089,RMVar_hsa_circ_205649,RMVar_hsa_circ_79158,RMVar_hsa_circ_205656,RMVar_hsa_circ_205657,RMVar_hsa_circ_98855,RMVar_hsa_circ_112496,RMVar_hsa_circ_205659,RMVar_hsa_circ_113648,RMVar_hsa_circ_357883,RMVar_hsa_circ_205663,RMVar_hsa_circ_205662,RMVar_hsa_circ_205664,RMVar_hsa_circ_205665,RMVar_hsa_circ_74879,RMVar_hsa_circ_116708,RMVar_hsa_circ_365688 28244 RMVar_ID_28244 Human_SNP_ID_108224377 A-to-I Human chr2 - 197413918 197413918 197413918 CCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCACTTGAACCCGGGAGGTGGAGGTT CCTGTAATCCCAGCTACTTGGGAGGCTGAGGCTGGAGAATCACTTGAACCCGGGAGGTGGAGGTT T A SF3B1 Ensembl:ENSG00000115524 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs546840432 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10010,RMVar_hsa_circ_120089,RMVar_hsa_circ_205649,RMVar_hsa_circ_79158,RMVar_hsa_circ_205656,RMVar_hsa_circ_205657,RMVar_hsa_circ_98855,RMVar_hsa_circ_112496,RMVar_hsa_circ_205659,RMVar_hsa_circ_113648,RMVar_hsa_circ_357883,RMVar_hsa_circ_205663,RMVar_hsa_circ_205662,RMVar_hsa_circ_205664,RMVar_hsa_circ_205665,RMVar_hsa_circ_74879,RMVar_hsa_circ_116708,RMVar_hsa_circ_365688 28245 RMVar_ID_28245 Human_SNP_ID_108224397 A-to-I Human chr2 - 197413983 197413983 197413983 GCCAACATGGTGAAAACCCCGACTCTAGTTAAAATACAAAAATTAGCCCGGCATGTTGGCGGGCA GCCAACATGGTGAAAACCCCGACTCTAGTTAAGATACAAAAATTAGCCCGGCATGTTGGCGGGCA T C SF3B1 Ensembl:ENSG00000115524 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1466447752 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10010,RMVar_hsa_circ_120089,RMVar_hsa_circ_205649,RMVar_hsa_circ_79158,RMVar_hsa_circ_205656,RMVar_hsa_circ_205657,RMVar_hsa_circ_98855,RMVar_hsa_circ_112496,RMVar_hsa_circ_205659,RMVar_hsa_circ_113648,RMVar_hsa_circ_357883,RMVar_hsa_circ_205663,RMVar_hsa_circ_205662,RMVar_hsa_circ_205664,RMVar_hsa_circ_205665,RMVar_hsa_circ_74879,RMVar_hsa_circ_116708,RMVar_hsa_circ_365688 28246 RMVar_ID_28246 Human_SNP_ID_108224594 A-to-I Human chr2 - 197414802 197414802 197414802 ACGGGTCTCACCATGTTGTCCAGGCTGATCTCAAACTCCTGGGCTTAAGCAGTCCATCTGCCTCA ACGGGTCTCACCATGTTGTCCAGGCTGATCTCGAACTCCTGGGCTTAAGCAGTCCATCTGCCTCA T C SF3B1 Ensembl:ENSG00000115524 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1319797939 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10010,RMVar_hsa_circ_120089,RMVar_hsa_circ_205649,RMVar_hsa_circ_79158,RMVar_hsa_circ_205656,RMVar_hsa_circ_205657,RMVar_hsa_circ_98855,RMVar_hsa_circ_112496,RMVar_hsa_circ_205659,RMVar_hsa_circ_113648,RMVar_hsa_circ_357883,RMVar_hsa_circ_205663,RMVar_hsa_circ_205662,RMVar_hsa_circ_205664,RMVar_hsa_circ_205665,RMVar_hsa_circ_74879,RMVar_hsa_circ_116708,RMVar_hsa_circ_365688 28247 RMVar_ID_28247 Human_SNP_ID_108224614 A-to-I Human chr2 - 197414882 197414882 197414882 TTCCCACCTCAACCCCCCAAGTAGATGGGACTATAGACACGTACCACCATGCCTGGCTAGTTTTT TTCCCACCTCAACCCCCCAAGTAGATGGGACTGTAGACACGTACCACCATGCCTGGCTAGTTTTT T C SF3B1 Ensembl:ENSG00000115524 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs957849493 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10010,RMVar_hsa_circ_120089,RMVar_hsa_circ_205649,RMVar_hsa_circ_79158,RMVar_hsa_circ_205656,RMVar_hsa_circ_205657,RMVar_hsa_circ_98855,RMVar_hsa_circ_112496,RMVar_hsa_circ_205659,RMVar_hsa_circ_113648,RMVar_hsa_circ_357883,RMVar_hsa_circ_205663,RMVar_hsa_circ_205662,RMVar_hsa_circ_205664,RMVar_hsa_circ_205665,RMVar_hsa_circ_74879,RMVar_hsa_circ_116708,RMVar_hsa_circ_365688 28248 RMVar_ID_28248 Human_SNP_ID_108224748 A-to-I Human chr2 - 197415358 197415358 197415358 GTACCAGCTACTTGGGAGGCTGAGACAGGAGAATCACTTGAACCTGGGAGGTGGAGGTTGTAGTG GTACCAGCTACTTGGGAGGCTGAGACAGGAGAGTCACTTGAACCTGGGAGGTGGAGGTTGTAGTG T C SF3B1 Ensembl:ENSG00000115524 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1009239965 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10010,RMVar_hsa_circ_120089,RMVar_hsa_circ_205649,RMVar_hsa_circ_79158,RMVar_hsa_circ_205656,RMVar_hsa_circ_205657,RMVar_hsa_circ_98855,RMVar_hsa_circ_112496,RMVar_hsa_circ_205659,RMVar_hsa_circ_113648,RMVar_hsa_circ_357883,RMVar_hsa_circ_205663,RMVar_hsa_circ_205662,RMVar_hsa_circ_205664,RMVar_hsa_circ_205665,RMVar_hsa_circ_74879,RMVar_hsa_circ_116708,RMVar_hsa_circ_365688 28249 RMVar_ID_28249 Human_SNP_ID_108228823 A-to-I Human chr2 - 197430852 197430852 197430852 AACATACAGAAAAGTAGAGAGCGGCTGGCGCTATACTCCAGCCTGGGCAACAGAGCAGGACTCTG AACATACAGAAAAGTAGAGAGCGGCTGGCGCTGTACTCCAGCCTGGGCAACAGAGCAGGACTCTG T C SF3B1 Ensembl:ENSG00000115524 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334428278 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_205657,RMVar_hsa_circ_98855 28250 RMVar_ID_28250 Human_SNP_ID_108228966 A-to-I Human chr2 - 197431210 197431210 197431210 GGGAGGCTGTTGCAGGAGAATCGCTTGAACCCAGGAGGCGAAGGTTGCAGTGAGCTGAGATCACG GGGAGGCTGTTGCAGGAGAATCGCTTGAACCCGGGAGGCGAAGGTTGCAGTGAGCTGAGATCACG T C SF3B1 Ensembl:ENSG00000115524 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1181550805 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_205657,RMVar_hsa_circ_98855 28251 RMVar_ID_28251 Human_SNP_ID_108240712 A-to-I Human chr2 + 197474635 197474634 197474635 TTGAACCCGGGAGGCGGAGGTTGCAGTTAGCCAAGATCGCCCTGCTGCACTCCAGCCTGGGCAAC TTGAACCCGGGAGGCGGAGGTTGCAGTTAGCC_AGATCGCCCTGCTGCACTCCAGCCTGGGCAAC CA C COQ10B Ensembl:ENSG00000115520 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs557701685 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_4591142 Human_miRNA_ID_2219940,Human_miRNA_ID_2482980,Human_miRNA_ID_3071355 RMVar_hsa_circ_78629,RMVar_hsa_circ_205674 28252 RMVar_ID_28252 Human_SNP_ID_108244097 A-to-I Human chr2 - 197487903 197487903 197487903 TCCTCAGAAGTTGGTTATGATGCTATGGCTGGAGATTTTGTGAATATGGTGGAAAAAGGAATCAT TCCTCAGAAGTTGGTTATGATGCTATGGCTGGGGATTTTGTGAATATGGTGGAAAAAGGAATCAT T C HSPD1 Ensembl:ENSG00000144381 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs773147194 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_280565,Human_RBP_ID_541411,Human_RBP_ID_1581810,Human_RBP_ID_1906744,Human_RBP_ID_3609727,Human_RBP_ID_5588904,Human_RBP_ID_6869168,Human_RBP_ID_8508466,Human_RBP_ID_8844569,Human_RBP_ID_9100332,Human_RBP_ID_13727326,Human_RBP_ID_17947161,Human_RBP_ID_18313167,Human_RBP_ID_18752140,Human_RBP_ID_21893934,Human_RBP_ID_22450047,Human_RBP_ID_22986773,Human_RBP_ID_23132575,Human_RBP_ID_23211799,Human_RBP_ID_23845894,Human_RBP_ID_26770422,Human_RBP_ID_27005274,Human_RBP_ID_27158381,Human_RBP_ID_27285219,Human_RBP_ID_27476572,Human_RBP_ID_27690728 Human_Splice_Rec_342321,Human_Splice_Rec_342341 Human_miRNA_ID_2972498,Human_miRNA_ID_2972499,Human_miRNA_ID_3005684,Human_miRNA_ID_3005685 RMVar_hsa_circ_90282,RMVar_hsa_circ_117452,RMVar_hsa_circ_126104,RMVar_hsa_circ_122650,RMVar_hsa_circ_98051,RMVar_hsa_circ_115375,RMVar_hsa_circ_92396,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_205680,RMVar_hsa_circ_205681,RMVar_hsa_circ_205679,RMVar_hsa_circ_357545,RMVar_hsa_circ_363144,RMVar_hsa_circ_366810,RMVar_hsa_circ_362939,RMVar_hsa_circ_57034 28253 RMVar_ID_28253 Human_SNP_ID_108244841 A-to-I Human chr2 - 197490646 197490646 197490646 TTTGTTATTTTCAGTAGAGACAGGGTTTCACCATCTTGGCCAGGCTGGTCTCGAACTCCTGACCT TTTGTTATTTTCAGTAGAGACAGGGTTTCACCGTCTTGGCCAGGCTGGTCTCGAACTCCTGACCT T C HSPD1 Ensembl:ENSG00000144381 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs542995536 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13727416 RMVar_hsa_circ_117452,RMVar_hsa_circ_122650,RMVar_hsa_circ_98051,RMVar_hsa_circ_115375,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_126781,RMVar_hsa_circ_357545,RMVar_hsa_circ_363144,RMVar_hsa_circ_362939,RMVar_hsa_circ_57034,RMVar_hsa_circ_81849,RMVar_hsa_circ_43808,RMVar_hsa_circ_14988,RMVar_hsa_circ_205687,RMVar_hsa_circ_205688,RMVar_hsa_circ_122492,RMVar_hsa_circ_373414,RMVar_hsa_circ_205690,RMVar_hsa_circ_205691,RMVar_hsa_circ_372815,RMVar_hsa_circ_205693 28254 RMVar_ID_28254 Human_SNP_ID_108245187 A-to-I Human chr2 - 197492001 197491997 197492001 ACACTTGCACAAGCACACTTGGCTGATCTTTTAATTTTTTTGTAGAGACGAGGTCTCAATATGTT ACACTTGCACAAGCACACTTGGCTGATCTTTT____TTTTTGTAGAGACGAGGTCTCAATATGTT AAATT A HSPD1 Ensembl:ENSG00000144381 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1034777258 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_13727487,Human_RBP_ID_17570104 RMVar_hsa_circ_117452,RMVar_hsa_circ_122650,RMVar_hsa_circ_98051,RMVar_hsa_circ_115375,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_126781,RMVar_hsa_circ_357545,RMVar_hsa_circ_363144,RMVar_hsa_circ_362939,RMVar_hsa_circ_57034,RMVar_hsa_circ_81849,RMVar_hsa_circ_43808,RMVar_hsa_circ_14988,RMVar_hsa_circ_205687,RMVar_hsa_circ_205688,RMVar_hsa_circ_122492,RMVar_hsa_circ_373414,RMVar_hsa_circ_205690,RMVar_hsa_circ_205691,RMVar_hsa_circ_372815,RMVar_hsa_circ_205693 28255 RMVar_ID_28255 Human_SNP_ID_108245206 A-to-I Human chr2 - 197492070 197492070 197492070 TCACTGCAGCCTTGAACTCTTGGGGTCAAGCAATCCTCCTGCCTCAGCCTCCCAAGTAGCTGGGA TCACTGCAGCCTTGAACTCTTGGGGTCAAGCAGTCCTCCTGCCTCAGCCTCCCAAGTAGCTGGGA T C HSPD1 Ensembl:ENSG00000144381 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs975135925 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117452,RMVar_hsa_circ_122650,RMVar_hsa_circ_98051,RMVar_hsa_circ_115375,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_126781,RMVar_hsa_circ_357545,RMVar_hsa_circ_363144,RMVar_hsa_circ_362939,RMVar_hsa_circ_57034,RMVar_hsa_circ_81849,RMVar_hsa_circ_43808,RMVar_hsa_circ_14988,RMVar_hsa_circ_205687,RMVar_hsa_circ_205688,RMVar_hsa_circ_122492,RMVar_hsa_circ_373414,RMVar_hsa_circ_205690,RMVar_hsa_circ_205691,RMVar_hsa_circ_372815,RMVar_hsa_circ_205693 28256 RMVar_ID_28256 Human_SNP_ID_108245298 A-to-I Human chr2 - 197492389 197492389 197492389 GATCAGGAGTTCCAGACCAGCCTGGCCAACATAGTGAAACCCCGTCTCTACTAAAAATATAAAAA GATCAGGAGTTCCAGACCAGCCTGGCCAACATCGTGAAACCCCGTCTCTACTAAAAATATAAAAA T G HSPD1 Ensembl:ENSG00000144381 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1266761635 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25496703 RMVar_hsa_circ_117452,RMVar_hsa_circ_122650,RMVar_hsa_circ_98051,RMVar_hsa_circ_115375,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_126781,RMVar_hsa_circ_357545,RMVar_hsa_circ_363144,RMVar_hsa_circ_362939,RMVar_hsa_circ_57034,RMVar_hsa_circ_81849,RMVar_hsa_circ_43808,RMVar_hsa_circ_14988,RMVar_hsa_circ_205687,RMVar_hsa_circ_205688,RMVar_hsa_circ_122492,RMVar_hsa_circ_373414,RMVar_hsa_circ_205690,RMVar_hsa_circ_205691,RMVar_hsa_circ_372815,RMVar_hsa_circ_205693 28257 RMVar_ID_28257 Human_SNP_ID_108246478 A-to-I Human chr2 - 197496854 197496854 197496854 CCAGGCTGGACTGCACTGGAACTCCTGGGCTCAAGCAATCCTCCTGCCTCAGCCTCCAAGTAGCT CCAGGCTGGACTGCACTGGAACTCCTGGGCTCGAGCAATCCTCCTGCCTCAGCCTCCAAGTAGCT T C HSPD1 Ensembl:ENSG00000144381 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1356749754 Functional Loss SNV dbSNP153 33..33 33 - - - 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 28258 RMVar_ID_28258 Human_SNP_ID_108246495 A-to-I Human chr2 - 197496908 197496908 197496908 TATTTTACTTAGTTGGTTTCTTTTGTTTTTAGAGACAGGGTCTTGCTCTGTAGCCCAGGCTGGAC TATTTTACTTAGTTGGTTTCTTTTGTTTTTAGGGACAGGGTCTTGCTCTGTAGCCCAGGCTGGAC T C HSPD1 Ensembl:ENSG00000144381 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1002897884 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6869250,Human_RBP_ID_8508517,Human_RBP_ID_13727746,Human_RBP_ID_24487548 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 28259 RMVar_ID_28259 Human_SNP_ID_108246496 A-to-I Human chr2 - 197496910 197496910 197496910 GATATTTTACTTAGTTGGTTTCTTTTGTTTTTAGAGACAGGGTCTTGCTCTGTAGCCCAGGCTGG GATATTTTACTTAGTTGGTTTCTTTTGTTTTTTGAGACAGGGTCTTGCTCTGTAGCCCAGGCTGG T A HSPD1 Ensembl:ENSG00000144381 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941730777 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6869250,Human_RBP_ID_8508517,Human_RBP_ID_13727746,Human_RBP_ID_22986838,Human_RBP_ID_24487548 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 28260 RMVar_ID_28260 Human_SNP_ID_108246497 A-to-I Human chr2 - 197496910 197496910 197496910 GATATTTTACTTAGTTGGTTTCTTTTGTTTTTAGAGACAGGGTCTTGCTCTGTAGCCCAGGCTGG GATATTTTACTTAGTTGGTTTCTTTTGTTTTTGGAGACAGGGTCTTGCTCTGTAGCCCAGGCTGG T C HSPD1 Ensembl:ENSG00000144381 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941730777 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6869250,Human_RBP_ID_8508517,Human_RBP_ID_13727746,Human_RBP_ID_22986838,Human_RBP_ID_24487548 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 28261 RMVar_ID_28261 Human_SNP_ID_108252961 A-to-I Human chr2 + 197519105 197519105 197519105 TTTAGTAGAGATGGGGTTTCAGCGTGTTAGCCAGGTTGGTCTCGAACTCCTGACCTCAAGTGATC TTTAGTAGAGATGGGGTTTCAGCGTGTTAGCCGGGTTGGTCTCGAACTCCTGACCTCAAGTGATC A G MOB4,HSPE1-MOB4 Ensembl:ENSG00000115540,Ensembl:ENSG00000270757 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1275833612 Functional Loss SNV dbSNP153 33..33 33 - - - 28262 RMVar_ID_28262 Human_SNP_ID_108253277 A-to-I Human chr2 + 197520375 197520375 197520375 GTTAGCCAGGATGGTCTCGATCTGCTGACCTCATGATCCGCCTGCCTCGGCCTCCCAAAGTGCTG GTTAGCCAGGATGGTCTCGATCTGCTGACCTCGTGATCCGCCTGCCTCGGCCTCCCAAAGTGCTG A G MOB4,HSPE1-MOB4 Ensembl:ENSG00000115540,Ensembl:ENSG00000270757 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs541286328 Functional Loss SNV dbSNP153 33..33 33 - - - 28263 RMVar_ID_28263 Human_SNP_ID_108258671 A-to-I Human chr2 + 197541073 197541073 197541073 CAGGCATGCGCTATCATGCCGGGCTAATTTTTATATTTTTAGTAGAGATGGGGTTTTGCTATATT CAGGCATGCGCTATCATGCCGGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTTGCTATATT A G MOB4,HSPE1-MOB4 Ensembl:ENSG00000115540,Ensembl:ENSG00000270757 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1559322641 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54656,RMVar_hsa_circ_54725,RMVar_hsa_circ_51695,RMVar_hsa_circ_350050,RMVar_hsa_circ_301741,RMVar_hsa_circ_205702 28264 RMVar_ID_28264 Human_SNP_ID_108259314 A-to-I Human chr2 + 197543762 197543761 197543763 TAGACTTTTTTCTTTTCTTTTCTTTTTGAGACAGAGTCTTGCTCTTTTGCCCAGGCTGGAGTTCA TAGACTTTTTTCTTTTCTTTTCTTTTTGAGAC__AGTCTTGCTCTTTTGCCCAGGCTGGAGTTCA CAG C MOB4,HSPE1-MOB4 Ensembl:ENSG00000115540,Ensembl:ENSG00000270757 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1464081148 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_54656,RMVar_hsa_circ_54725,RMVar_hsa_circ_51695,RMVar_hsa_circ_350050,RMVar_hsa_circ_301741,RMVar_hsa_circ_205702 28265 RMVar_ID_28265 Human_SNP_ID_108261942 A-to-I Human chr2 + 197554796 197554796 197554796 TAAAAATACAAAAACTAGCTGGGTGTGGTGATACGCACTTATAAACCCAGCTACTTGGGAGGCTG TAAAAATACAAAAACTAGCTGGGTGTGGTGATGCGCACTTATAAACCCAGCTACTTGGGAGGCTG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909527348 Functional Loss SNV dbSNP153 33..33 33 - - - 28266 RMVar_ID_28266 Human_SNP_ID_108262100 A-to-I Human chr2 + 197555276 197555276 197555276 TCAAGCGATTCTCCTGCCTCAGCCTTCCAAGTAGTTGGGACTACAGGCCTGCACCACCGCACCAT TCAAGCGATTCTCCTGCCTCAGCCTTCCAAGTGGTTGGGACTACAGGCCTGCACCACCGCACCAT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1306717212 Functional Loss SNV dbSNP153 33..33 33 - - - 28267 RMVar_ID_28267 Human_SNP_ID_108289370 A-to-I Human chr2 - 197664690 197664690 197664690 ACCTTGACCTCCCAGGCTCAAGTGATCCTCCCACCTCAGCCTCCCAAGTAGCCGGGACCACAACC ACCTTGACCTCCCAGGCTCAAGTGATCCTCCCGCCTCAGCCTCCCAAGTAGCCGGGACCACAACC T C RFTN2 Ensembl:ENSG00000162944 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1001224760 Functional Loss SNV dbSNP153 33..33 33 - - - 28268 RMVar_ID_28268 Human_SNP_ID_108303158 A-to-I Human chr2 + 197717427 197717427 197717427 ATAAAAAATAAATAAAAATAACTGCAGAACTCAGGCCTGTAATCCCAGCACTTTGGGAGGCTGAG ATAAAAAATAAATAAAAATAACTGCAGAACTCGGGCCTGTAATCCCAGCACTTTGGGAGGCTGAG A G AC011997.1 Ensembl:ENSG00000222017 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs780728842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13729444 28269 RMVar_ID_28269 Human_SNP_ID_108797746 A-to-I Human chr2 - 199803004 199803000 199803004 TTTCTTTTTATTTTTAATAGGGATGAATTCTCACTCTGTTGCCCAGGCTGGTCTTGAATTCCTGA TTTCTTTTTATTTTTAATAGGGATGAATTCTC____TGTTGCCCAGGCTGGTCTTGAATTCCTGA AGAGT A FTCDNL1 Ensembl:ENSG00000226124 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1052611122 Functional Loss DEL dbSNP153 33..36 33 - - - 28270 RMVar_ID_28270 Human_SNP_ID_108822828 A-to-I Human chr2 + 199913622 199913622 199913622 CTCAAAATAATTGACTGGTTTAGTTGACTGCTAATAAAAACTGGAGAAAAAAAAAGAGAATAAAG CTCAAAATAATTGACTGGTTTAGTTGACTGCTGATAAAAACTGGAGAAAAAAAAAGAGAATAAAG A G C2orf69 Ensembl:ENSG00000178074 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1182594206 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_205772,RMVar_hsa_circ_92382 28271 RMVar_ID_28271 Human_SNP_ID_108825065 A-to-I Human chr2 + 199923081 199923081 199923081 GGCAAGCTCCCACCTCAGGGCGTTTTGCAGTTACAGTTCCTTCTGCCTGAAATACCCACGTGGTT GGCAAGCTCCCACCTCAGGGCGTTTTGCAGTTGCAGTTCCTTCTGCCTGAAATACCCACGTGGTT A G C2orf69 Ensembl:ENSG00000178074 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs281760 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2805,GWAS_ID_2806,GWAS_ID_2807,GWAS_ID_2808,GWAS_ID_2809,GWAS_ID_2810,GWAS_ID_2811,GWAS_ID_2812,GWAS_ID_2813,GWAS_ID_2814,GWAS_ID_2815,GWAS_ID_2816,GWAS_ID_2817,GWAS_ID_2818,GWAS_ID_2819,GWAS_ID_2820,GWAS_ID_2821,GWAS_ID_2822,GWAS_ID_2823,GWAS_ID_2824,GWAS_ID_2825,GWAS_ID_2826,GWAS_ID_2827,GWAS_ID_2828,GWAS_ID_2829,GWAS_ID_2830,GWAS_ID_2831,GWAS_ID_2832,GWAS_ID_2833,GWAS_ID_2834,GWAS_ID_2835,GWAS_ID_2836,GWAS_ID_2837,GWAS_ID_2838,GWAS_ID_2839,GWAS_ID_2840,GWAS_ID_2841,GWAS_ID_2842,GWAS_ID_2843,GWAS_ID_2844,GWAS_ID_2845,GWAS_ID_2846,GWAS_ID_2847,GWAS_ID_2848,GWAS_ID_2849,GWAS_ID_2850,GWAS_ID_2851,GWAS_ID_2852,GWAS_ID_2853,GWAS_ID_2854,GWAS_ID_2855,GWAS_ID_2856,GWAS_ID_2857,GWAS_ID_2858,GWAS_ID_2859 RMVar_hsa_circ_205772,RMVar_hsa_circ_92382 28272 RMVar_ID_28272 Human_SNP_ID_108828433 A-to-I Human chr2 - 199937412 199937412 199937412 GTAATCCGCCCACCTCGACCTCCCAAAGTACTAGGATTACAGGCATGAGCCACCATGCCTGGCCT GTAATCCGCCCACCTCGACCTCCCAAAGTACTGGGATTACAGGCATGAGCCACCATGCCTGGCCT T C TYW5 Ensembl:ENSG00000162971 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1315887630 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27853,RMVar_hsa_circ_205775,RMVar_hsa_circ_287172 28273 RMVar_ID_28273 Human_SNP_ID_108835100 A-to-I Human chr2 + 199965587 199965587 199965587 CCACGTGCTTGGGAGACTGAGATGGGAGGATCACCTGAGCCTGGAGAGGTTGAGGCTGCACTGAG CCACGTGCTTGGGAGACTGAGATGGGAGGATCGCCTGAGCCTGGAGAGGTTGAGGCTGCACTGAG A G MAIP1 Ensembl:ENSG00000162972 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs922249886 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8508851 28274 RMVar_ID_28274 Human_SNP_ID_108836515 A-to-I Human chr2 + 199972955 199972955 199972955 CATACTCACTGCAGCCTTGAACCCCTGTGCTCAAATGATCTTTCCACCTCAGCCTTCCAAAGTGC CATACTCACTGCAGCCTTGAACCCCTGTGCTCCAATGATCTTTCCACCTCAGCCTTCCAAAGTGC A C MAIP1 Ensembl:ENSG00000162972 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1241953128 Functional Loss SNV dbSNP153 33..33 33 - - - 28275 RMVar_ID_28275 Human_SNP_ID_108930155 A-to-I Human chr2 + 200388451 200388451 200388451 AAAATTAGCTGAGTGTGGTGGTGCATACCTGCAGTTCCACCTACTTGGGAGGCTGAGGTGGCAGG AAAATTAGCTGAGTGTGGTGGTGCATACCTGCGGTTCCACCTACTTGGGAGGCTGAGGTGGCAGG A G SPATS2L Ensembl:ENSG00000196141 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs933478393 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59766,RMVar_hsa_circ_294151,RMVar_hsa_circ_365709,RMVar_hsa_circ_349935,RMVar_hsa_circ_358282,RMVar_hsa_circ_303260,RMVar_hsa_circ_107019,RMVar_hsa_circ_278481,RMVar_hsa_circ_69317,RMVar_hsa_circ_53312,RMVar_hsa_circ_205783,RMVar_hsa_circ_205784,RMVar_hsa_circ_316842,RMVar_hsa_circ_368632,RMVar_hsa_circ_72072 28276 RMVar_ID_28276 Human_SNP_ID_108930175 A-to-I Human chr2 + 200388527 200388527 200388527 TGAGGAGATGGAGGCTGCAGTGAACTGCGATCACGCCACTGCATTCCAGCCTGGGCAACAGGTAG TGAGGAGATGGAGGCTGCAGTGAACTGCGATCGCGCCACTGCATTCCAGCCTGGGCAACAGGTAG A G SPATS2L Ensembl:ENSG00000196141 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs762403701 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59766,RMVar_hsa_circ_294151,RMVar_hsa_circ_365709,RMVar_hsa_circ_349935,RMVar_hsa_circ_358282,RMVar_hsa_circ_303260,RMVar_hsa_circ_107019,RMVar_hsa_circ_278481,RMVar_hsa_circ_69317,RMVar_hsa_circ_53312,RMVar_hsa_circ_205783,RMVar_hsa_circ_205784,RMVar_hsa_circ_316842,RMVar_hsa_circ_368632,RMVar_hsa_circ_72072 28277 RMVar_ID_28277 Human_SNP_ID_108946485 A-to-I Human chr2 + 200464747 200464747 200464747 GCAATCCTCCTGCCTCAGCCTCCGAAAGTGCTAAGATAACATGTGTGAGCCACTGCGCCTGGCAA GCAATCCTCCTGCCTCAGCCTCCGAAAGTGCTGAGATAACATGTGTGAGCCACTGCGCCTGGCAA A G SPATS2L Ensembl:ENSG00000196141 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1185254443 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59766,RMVar_hsa_circ_107541,RMVar_hsa_circ_6883,RMVar_hsa_circ_205787,RMVar_hsa_circ_205791,RMVar_hsa_circ_41486 28278 RMVar_ID_28278 Human_SNP_ID_108965099 A-to-I Human chr2 + 200544471 200544471 200544471 TCTTGGCTAATTTTTGTATTTTTAATAGGGACAGGATTTTACCATGTTGGCCAGGCTGATCTCCA TCTTGGCTAATTTTTGTATTTTTAATAGGGACTGGATTTTACCATGTTGGCCAGGCTGATCTCCA A T SGO2 Ensembl:ENSG00000163535 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1394745224 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64566,RMVar_hsa_circ_46524 28279 RMVar_ID_28279 Human_SNP_ID_109029777 A-to-I Human chr2 + 200819207 200819207 200819207 TGAGCTCAGTTTAAGACGTGCCTGGGCAACATAGTGAGACCTCATCTCTACTAAAAATCACAAAA TGAGCTCAGTTTAAGACGTGCCTGGGCAACATGGTGAGACCTCATCTCTACTAAAAATCACAAAA A G BZW1 Ensembl:ENSG00000082153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs993805092 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13417,RMVar_hsa_circ_21993,RMVar_hsa_circ_115973,RMVar_hsa_circ_84153,RMVar_hsa_circ_205813,RMVar_hsa_circ_360355,RMVar_hsa_circ_362921,RMVar_hsa_circ_205814,RMVar_hsa_circ_205815 28280 RMVar_ID_28280 Human_SNP_ID_109039904 A-to-I Human chr2 - 200855397 200855397 200855397 AGGATGGTCTTGATCTCCTGCCCTCGTGTTCCACCTGCCTCAGCCTCCCAAAGGGCTGGGATTAT AGGATGGTCTTGATCTCCTGCCCTCGTGTTCCGCCTGCCTCAGCCTCCCAAAGGGCTGGGATTAT T C CLK1 Ensembl:ENSG00000013441 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs907814933 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_984,RMVar_hsa_circ_31004,RMVar_hsa_circ_101138,RMVar_hsa_circ_323670,RMVar_hsa_circ_274777,RMVar_hsa_circ_205819,RMVar_hsa_circ_205820,RMVar_hsa_circ_205818,RMVar_hsa_circ_205821,RMVar_hsa_circ_49580,RMVar_hsa_circ_307682 28281 RMVar_ID_28281 Human_SNP_ID_109040114 A-to-I Human chr2 - 200855962 200855962 200855962 CTCTGTCGCCCAGGCTGGAGTGCAGTGGTGCAATCTTGGCTCACTGCAACTTCTGCCTCCTGGGT CTCTGTCGCCCAGGCTGGAGTGCAGTGGTGCAGTCTTGGCTCACTGCAACTTCTGCCTCCTGGGT T C CLK1 Ensembl:ENSG00000013441 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1020805820 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_984,RMVar_hsa_circ_31004,RMVar_hsa_circ_101138,RMVar_hsa_circ_323670,RMVar_hsa_circ_274777,RMVar_hsa_circ_205819,RMVar_hsa_circ_205820,RMVar_hsa_circ_205818,RMVar_hsa_circ_205821,RMVar_hsa_circ_49580,RMVar_hsa_circ_307682 28282 RMVar_ID_28282 Human_SNP_ID_109045596 A-to-I Human chr2 - 200874868 200874868 200874868 TAAAAATTATCCAGGTGTGGTGGCTCACACCTATGGTCCCAGCTACTTGGGAGGCTGAAGTGAGA TAAAAATTATCCAGGTGTGGTGGCTCACACCTGTGGTCCCAGCTACTTGGGAGGCTGAAGTGAGA T C PPIL3 Ensembl:ENSG00000240344 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs944471832 Functional Loss SNV dbSNP153 33..33 33 - - - 28283 RMVar_ID_28283 Human_SNP_ID_109045599 A-to-I Human chr2 - 200874888 200874888 200874888 CCCGTCTCTACAAAAAAATTTAAAAATTATCCAGGTGTGGTGGCTCACACCTATGGTCCCAGCTA CCCGTCTCTACAAAAAAATTTAAAAATTATCCTGGTGTGGTGGCTCACACCTATGGTCCCAGCTA T A PPIL3 Ensembl:ENSG00000240344 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991771130 Functional Loss SNV dbSNP153 33..33 33 - - - 28284 RMVar_ID_28284 Human_SNP_ID_109046719 A-to-I Human chr2 - 200879296 200879294 200879297 GCTAACACAGTGAAACCCCGTCTCTGCCAAAAAATACAAAAAATTAGCCAGGTGTGGTGGTGGGT GCTAACACAGTGAAACCCCGTCTCTGCCAAA___TACAAAAAATTAGCCAGGTGTGGTGGTGGGT ATTT A PPIL3 Ensembl:ENSG00000240344 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs573535875 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_17340,RMVar_hsa_circ_315000,RMVar_hsa_circ_282766,RMVar_hsa_circ_6316,RMVar_hsa_circ_205829,RMVar_hsa_circ_205830 28285 RMVar_ID_28285 Human_SNP_ID_109046994 A-to-I Human chr2 - 200880538 200880538 200880538 TCCACAAAAAAATACAAATATTAGCCTGTTATAGTGGCGTGTGCCTGTAGTCCCAGCTACTCAAG TCCACAAAAAAATACAAATATTAGCCTGTTATGGTGGCGTGTGCCTGTAGTCCCAGCTACTCAAG T C PPIL3 Ensembl:ENSG00000240344 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1220591695 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17340,RMVar_hsa_circ_315000,RMVar_hsa_circ_282766,RMVar_hsa_circ_6316,RMVar_hsa_circ_205829,RMVar_hsa_circ_205830 28286 RMVar_ID_28286 Human_SNP_ID_109047503 A-to-I Human chr2 - 200882823 200882823 200882823 CGATCTCGGCTCACTGCAACCTCCGCCTCCCAAGTTCACGCCATTCTCCTCCCTCAGCCTCCAGA CGATCTCGGCTCACTGCAACCTCCGCCTCCCAGGTTCACGCCATTCTCCTCCCTCAGCCTCCAGA T C PPIL3 Ensembl:ENSG00000240344 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1006506701 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17340,RMVar_hsa_circ_282766,RMVar_hsa_circ_108546,RMVar_hsa_circ_205830,RMVar_hsa_circ_205832 28287 RMVar_ID_28287 Human_SNP_ID_109047684 A-to-I Human chr2 - 200883501 200883501 200883501 GATCTTCCTGCCTCCCAAAGTGCTGAGATTACAGGTGTGAGCTGCTGTGCCTGGCCTAAAATTAA GATCTTCCTGCCTCCCAAAGTGCTGAGATTACGGGTGTGAGCTGCTGTGCCTGGCCTAAAATTAA T C PPIL3 Ensembl:ENSG00000240344 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs527662186 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22596925 RMVar_hsa_circ_17340,RMVar_hsa_circ_282766,RMVar_hsa_circ_108546,RMVar_hsa_circ_205830,RMVar_hsa_circ_205832 28288 RMVar_ID_28288 Human_SNP_ID_109047690 A-to-I Human chr2 - 200883536 200883536 200883536 TTGCCCAGGCTGGTCTTGAACTCCTGGACTCAAGTGATCTTCCTGCCTCCCAAAGTGCTGAGATT TTGCCCAGGCTGGTCTTGAACTCCTGGACTCAGGTGATCTTCCTGCCTCCCAAAGTGCTGAGATT T C PPIL3 Ensembl:ENSG00000240344 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1254657187 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17340,RMVar_hsa_circ_282766,RMVar_hsa_circ_108546,RMVar_hsa_circ_205830,RMVar_hsa_circ_205832 28289 RMVar_ID_28289 Human_SNP_ID_109047693 A-to-I Human chr2 - 200883571 200883571 200883571 TTTTTTTTTAAAGATAGAGATGAGGTCTTACTATGTTGCCCAGGCTGGTCTTGAACTCCTGGACT TTTTTTTTTAAAGATAGAGATGAGGTCTTACTCTGTTGCCCAGGCTGGTCTTGAACTCCTGGACT T G PPIL3 Ensembl:ENSG00000240344 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs893431875 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17340,RMVar_hsa_circ_282766,RMVar_hsa_circ_108546,RMVar_hsa_circ_205830,RMVar_hsa_circ_205832 28290 RMVar_ID_28290 Human_SNP_ID_109047796 A-to-I Human chr2 - 200884027 200884027 200884027 TTATTTATGGCTGGGCATGGTGGCTCACATCTATAATTCCAGCACTTTGGGAGGCTAAGGTGAGC TTATTTATGGCTGGGCATGGTGGCTCACATCTGTAATTCCAGCACTTTGGGAGGCTAAGGTGAGC T C PPIL3 Ensembl:ENSG00000240344 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1483476706 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17340,RMVar_hsa_circ_282766,RMVar_hsa_circ_108546,RMVar_hsa_circ_205830,RMVar_hsa_circ_205832 28291 RMVar_ID_28291 Human_SNP_ID_109047799 A-to-I Human chr2 - 200884031 200884031 200884031 GCAATTATTTATGGCTGGGCATGGTGGCTCACATCTATAATTCCAGCACTTTGGGAGGCTAAGGT GCAATTATTTATGGCTGGGCATGGTGGCTCACGTCTATAATTCCAGCACTTTGGGAGGCTAAGGT T C PPIL3 Ensembl:ENSG00000240344 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1208005259 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17340,RMVar_hsa_circ_282766,RMVar_hsa_circ_108546,RMVar_hsa_circ_205830,RMVar_hsa_circ_205832 28292 RMVar_ID_28292 Human_SNP_ID_109047880 A-to-I Human chr2 - 200884280 200884280 200884280 CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTATAGGCGCCAGCCACCATGCCCAGCTAATTTTG CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTGTAGGCGCCAGCCACCATGCCCAGCTAATTTTG T C PPIL3 Ensembl:ENSG00000240344 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs927692237 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17340,RMVar_hsa_circ_282766,RMVar_hsa_circ_108546,RMVar_hsa_circ_205830,RMVar_hsa_circ_205832 28293 RMVar_ID_28293 Human_SNP_ID_109048040 A-to-I Human chr2 - 200884881 200884881 200884881 TTATATTTTTTTAGTAGAGACGGGGTTTCACCATGTTGACCAGGCTGGTCTCAAACTTCTGACCT TTATATTTTTTTAGTAGAGACGGGGTTTCACCGTGTTGACCAGGCTGGTCTCAAACTTCTGACCT T C PPIL3 Ensembl:ENSG00000240344 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335441543 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17340,RMVar_hsa_circ_282766,RMVar_hsa_circ_108546,RMVar_hsa_circ_205830,RMVar_hsa_circ_205832 28294 RMVar_ID_28294 Human_SNP_ID_109048157 A-to-I Human chr2 - 200885258 200885258 200885258 CAAGCAAGTCTTCTGCCTCAGCCTCCCGAGTAAGTGGGATTACAGGCGTGCGCCACCATGCCTGG CAAGCAAGTCTTCTGCCTCAGCCTCCCGAGTACGTGGGATTACAGGCGTGCGCCACCATGCCTGG T G PPIL3 Ensembl:ENSG00000240344 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1460529346 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_344614 RMVar_hsa_circ_17340,RMVar_hsa_circ_282766,RMVar_hsa_circ_108546,RMVar_hsa_circ_205830,RMVar_hsa_circ_205832 28295 RMVar_ID_28295 Human_SNP_ID_109048188 A-to-I Human chr2 - 200885335 200885335 200885335 ATGGAGTCTCGCTGTGTCCCCCAGGCTGGAGTACAATGGCGCGATCTCGGCTCACTGCAACCTCC ATGGAGTCTCGCTGTGTCCCCCAGGCTGGAGTGCAATGGCGCGATCTCGGCTCACTGCAACCTCC T C PPIL3 Ensembl:ENSG00000240344 Protein coding intron GSE38233;GSE56152 cultured B-cells;embryonic stem cells,wild type - 24183664,25708366 RNA-Seq:(High) rs1435207324 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_344572,Human_Splice_Rec_344573,Human_Splice_Rec_344614,Human_Splice_Rec_344615,Human_Splice_Rec_344626,Human_Splice_Rec_344627,Human_Splice_Rec_344674,Human_Splice_Rec_344675,Human_Splice_Rec_344682,Human_Splice_Rec_344688 RMVar_hsa_circ_17340,RMVar_hsa_circ_282766,RMVar_hsa_circ_108546,RMVar_hsa_circ_205830,RMVar_hsa_circ_205832 28296 RMVar_ID_28296 Human_SNP_ID_109049572 A-to-I Human chr2 + 200890148 200890148 200890148 TGGAGGCCGAGGCAGGTGGATCACTTGAGCGCAGGAGTTTGAGACCAGCCTGGGCAACATGGCGA TGGAGGCCGAGGCAGGTGGATCACTTGAGCGCGGGAGTTTGAGACCAGCCTGGGCAACATGGCGA A G NIF3L1 Ensembl:ENSG00000196290 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs981637993 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25498668 28297 RMVar_ID_28297 Human_SNP_ID_109049576 A-to-I Human chr2 + 200890193 200890193 200890193 CAGCCTGGGCAACATGGCGAATCCCCATCTCTACTAAAAATACAAAAATTAGCCAGGTGTGGTGT CAGCCTGGGCAACATGGCGAATCCCCATCTCTGCTAAAAATACAAAAATTAGCCAGGTGTGGTGT A G NIF3L1 Ensembl:ENSG00000196290 Protein coding intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs907235820 Functional Loss SNV dbSNP153 33..33 33 - - - 28298 RMVar_ID_28298 Human_SNP_ID_109049589 A-to-I Human chr2 + 200890237 200890237 200890237 AAAATTAGCCAGGTGTGGTGTTTAGCGCCTGTAGTCCCAGCTGCTCAGGAGGCTGAGGTGGGAGG AAAATTAGCCAGGTGTGGTGTTTAGCGCCTGTGGTCCCAGCTGCTCAGGAGGCTGAGGTGGGAGG A G NIF3L1 Ensembl:ENSG00000196290 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1260956019 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23847136 28299 RMVar_ID_28299 Human_SNP_ID_109049597 A-to-I Human chr2 + 200890284 200890284 200890284 GGAGGCTGAGGTGGGAGGATCTGCTTGAGCTCAGGAAGTCGAGGCTGCAGTGAGCTGAGATCACG GGAGGCTGAGGTGGGAGGATCTGCTTGAGCTCTGGAAGTCGAGGCTGCAGTGAGCTGAGATCACG A T NIF3L1 Ensembl:ENSG00000196290 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1490669784 Functional Loss SNV dbSNP153 33..33 33 - - - 28300 RMVar_ID_28300 Human_SNP_ID_109049833 A-to-I Human chr2 + 200891215 200891215 200891215 TTGACTTTGTGATCCTCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGCCCCGCCACATT TTGACTTTGTGATCCTCCCGCCTCGGCCTCCCGAAGTGCTGGGATTACAGGCGCCCCGCCACATT A G NIF3L1 Ensembl:ENSG00000196290 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285048872 Functional Loss SNV dbSNP153 33..33 33 - - - 28301 RMVar_ID_28301 Human_SNP_ID_109054177 A-to-I Human chr2 - 200909512 200909512 200909512 TTTAGCAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAATTCCTGACCTCAAGTGATC TTTAGCAGAGATGGGGTTTCACCATGTTGGCCTGGCTGGTCTCGAATTCCTGACCTCAAGTGATC T A ORC2 Ensembl:ENSG00000115942 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs924062166 Functional Loss SNV dbSNP153 33..33 33 - - - 28302 RMVar_ID_28302 Human_SNP_ID_109054179 A-to-I Human chr2 - 200909521 200909521 200909521 TTTTGAATTTTTAGCAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAATTCCTGACCT TTTTGAATTTTTAGCAGAGATGGGGTTTCACCGTGTTGGCCAGGCTGGTCTCGAATTCCTGACCT T C ORC2 Ensembl:ENSG00000115942 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs1322159844 Functional Loss SNV dbSNP153 33..33 33 - - - 28303 RMVar_ID_28303 Human_SNP_ID_109054185 A-to-I Human chr2 - 200909538 200909538 200909538 CACCACGCCTGGCTAGTTTTTGAATTTTTAGCAGAGATGGGGTTTCACCATGTTGGCCAGGCTGG CACCACGCCTGGCTAGTTTTTGAATTTTTAGCGGAGATGGGGTTTCACCATGTTGGCCAGGCTGG T C ORC2 Ensembl:ENSG00000115942 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1459233990 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25498741 28304 RMVar_ID_28304 Human_SNP_ID_109054205 A-to-I Human chr2 - 200909618 200909618 200909618 AAGCTTACAGCAGCCTCCACCTCCTGGGTTCAAGTGATTCTTGTGCCTCAGCCTCCTGAGCTGGG AAGCTTACAGCAGCCTCCACCTCCTGGGTTCAGGTGATTCTTGTGCCTCAGCCTCCTGAGCTGGG T C ORC2 Ensembl:ENSG00000115942 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1325545675 Functional Loss SNV dbSNP153 33..33 33 - - - 28305 RMVar_ID_28305 Human_SNP_ID_109054206 A-to-I Human chr2 - 200909619 200909619 200909619 TAAGCTTACAGCAGCCTCCACCTCCTGGGTTCAAGTGATTCTTGTGCCTCAGCCTCCTGAGCTGG TAAGCTTACAGCAGCCTCCACCTCCTGGGTTCGAGTGATTCTTGTGCCTCAGCCTCCTGAGCTGG T C ORC2 Ensembl:ENSG00000115942 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs180899938 Functional Loss SNV dbSNP153 33..33 33 - - - 28306 RMVar_ID_28306 Human_SNP_ID_109054207 A-to-I Human chr2 - 200909619 200909619 200909619 TAAGCTTACAGCAGCCTCCACCTCCTGGGTTCAAGTGATTCTTGTGCCTCAGCCTCCTGAGCTGG TAAGCTTACAGCAGCCTCCACCTCCTGGGTTCCAGTGATTCTTGTGCCTCAGCCTCCTGAGCTGG T G ORC2 Ensembl:ENSG00000115942 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs180899938 Functional Loss SNV dbSNP153 33..33 33 - - - 28307 RMVar_ID_28307 Human_SNP_ID_109054291 A-to-I Human chr2 - 200909902 200909902 200909902 AAAAAATCATCCGGGCATGGTGGCCCATGCCTATAGTCCTAGCTGCTGTGGAGGCTGAGGCAGGA AAAAAATCATCCGGGCATGGTGGCCCATGCCTGTAGTCCTAGCTGCTGTGGAGGCTGAGGCAGGA T C ORC2 Ensembl:ENSG00000115942 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1230781563 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17698033 28308 RMVar_ID_28308 Human_SNP_ID_109054294 A-to-I Human chr2 - 200909918 200909918 200909918 TCTCTACAAAAAATTTAAAAAATCATCCGGGCATGGTGGCCCATGCCTATAGTCCTAGCTGCTGT TCTCTACAAAAAATTTAAAAAATCATCCGGGCCTGGTGGCCCATGCCTATAGTCCTAGCTGCTGT T G ORC2 Ensembl:ENSG00000115942 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1181179606 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17698033 28309 RMVar_ID_28309 Human_SNP_ID_109054308 A-to-I Human chr2 - 200909982 200909982 200909982 AAGGCAGGAGGATCTCTGGAGCCCAGGAGTTTAAGAACAGCCTGGGCAACATAGTGAGACCTTGT AAGGCAGGAGGATCTCTGGAGCCCAGGAGTTTGAGAACAGCCTGGGCAACATAGTGAGACCTTGT T C ORC2 Ensembl:ENSG00000115942 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs374210531 Functional Loss SNV dbSNP153 33..33 33 - - - 28310 RMVar_ID_28310 Human_SNP_ID_109055375 A-to-I Human chr2 - 200914657 200914657 200914657 TTTGCACCTCAGCCTCCCGAGTAGCTGAGACCATAGGCGCATACCAGTATGCCTGGCTAATTTTT TTTGCACCTCAGCCTCCCGAGTAGCTGAGACCGTAGGCGCATACCAGTATGCCTGGCTAATTTTT T C ORC2 Ensembl:ENSG00000115942 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1227073815 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88415,RMVar_hsa_circ_70109,RMVar_hsa_circ_296317,RMVar_hsa_circ_349372,RMVar_hsa_circ_268470,RMVar_hsa_circ_34864,RMVar_hsa_circ_88925,RMVar_hsa_circ_205836,RMVar_hsa_circ_205837,RMVar_hsa_circ_205838 28311 RMVar_ID_28311 Human_SNP_ID_109055678 A-to-I Human chr2 - 200915818 200915816 200915818 GTGGTGGTGTCCACCTGTAATCGCAACTACTCAGGAGTCTGAGGCATGAAAATCGCTTGAACCTG GTGGTGGTGTCCACCTGTAATCGCAACTACTC__GAGTCTGAGGCATGAAAATCGCTTGAACCTG CCT C ORC2 Ensembl:ENSG00000115942 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1310817383 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_1907371,Human_RBP_ID_13736131 RMVar_hsa_circ_88415,RMVar_hsa_circ_70109,RMVar_hsa_circ_296317,RMVar_hsa_circ_349372,RMVar_hsa_circ_268470,RMVar_hsa_circ_34864,RMVar_hsa_circ_88925,RMVar_hsa_circ_205836,RMVar_hsa_circ_205837,RMVar_hsa_circ_205838 28312 RMVar_ID_28312 Human_SNP_ID_109056253 A-to-I Human chr2 - 200918284 200918284 200918284 AATACCCTGGCTCAAAATACAAACATCTCAATACAACAGAATGATAAATCAGTGAGCAGAGTTGA AATACCCTGGCTCAAAATACAAACATCTCAATTCAACAGAATGATAAATCAGTGAGCAGAGTTGA T A ORC2 Ensembl:ENSG00000115942 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1912331 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2860,GWAS_ID_2861 RMVar_hsa_circ_88415,RMVar_hsa_circ_70109,RMVar_hsa_circ_296317,RMVar_hsa_circ_349372,RMVar_hsa_circ_268470,RMVar_hsa_circ_34864,RMVar_hsa_circ_88925,RMVar_hsa_circ_205836,RMVar_hsa_circ_205837,RMVar_hsa_circ_205838 28313 RMVar_ID_28313 Human_SNP_ID_109056254 A-to-I Human chr2 - 200918284 200918284 200918284 AATACCCTGGCTCAAAATACAAACATCTCAATACAACAGAATGATAAATCAGTGAGCAGAGTTGA AATACCCTGGCTCAAAATACAAACATCTCAATGCAACAGAATGATAAATCAGTGAGCAGAGTTGA T C ORC2 Ensembl:ENSG00000115942 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1912331 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2860,GWAS_ID_2861 RMVar_hsa_circ_88415,RMVar_hsa_circ_70109,RMVar_hsa_circ_296317,RMVar_hsa_circ_349372,RMVar_hsa_circ_268470,RMVar_hsa_circ_34864,RMVar_hsa_circ_88925,RMVar_hsa_circ_205836,RMVar_hsa_circ_205837,RMVar_hsa_circ_205838 28314 RMVar_ID_28314 Human_SNP_ID_109058456 A-to-I Human chr2 - 200928347 200928347 200928347 GAATAAATATTTATTTATTTATTTAAGATGGAATCTTACTCTGTTGCCCAGGCTGGAATGTAGTG GAATAAATATTTATTTATTTATTTAAGATGGAGTCTTACTCTGTTGCCCAGGCTGGAATGTAGTG T C ORC2 Ensembl:ENSG00000115942 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1329616497 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_205840,RMVar_hsa_circ_70109,RMVar_hsa_circ_296317,RMVar_hsa_circ_349372,RMVar_hsa_circ_268470,RMVar_hsa_circ_88925,RMVar_hsa_circ_205836,RMVar_hsa_circ_297081,RMVar_hsa_circ_205838,RMVar_hsa_circ_372574,RMVar_hsa_circ_375146,RMVar_hsa_circ_369093,RMVar_hsa_circ_16713,RMVar_hsa_circ_46803,RMVar_hsa_circ_205842,RMVar_hsa_circ_205841,RMVar_hsa_circ_205845,RMVar_hsa_circ_331027,RMVar_hsa_circ_359605,RMVar_hsa_circ_205839,RMVar_hsa_circ_361803,RMVar_hsa_circ_353783,RMVar_hsa_circ_329435,RMVar_hsa_circ_295020,RMVar_hsa_circ_298578,RMVar_hsa_circ_205846,RMVar_hsa_circ_72876,RMVar_hsa_circ_205844 28315 RMVar_ID_28315 Human_SNP_ID_109062241 A-to-I Human chr2 - 200945384 200945384 200945384 CCTGGCTAATTTTTCTATTCTTTTGTAGAGACAGGGTTTCTTCATGTTGCCCAGTCTGGTCTCGA CCTGGCTAATTTTTCTATTCTTTTGTAGAGACGGGGTTTCTTCATGTTGCCCAGTCTGGTCTCGA T C ORC2 Ensembl:ENSG00000115942 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs370658693 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_205840,RMVar_hsa_circ_349372,RMVar_hsa_circ_88925,RMVar_hsa_circ_205838,RMVar_hsa_circ_372574,RMVar_hsa_circ_369093,RMVar_hsa_circ_16713,RMVar_hsa_circ_46803,RMVar_hsa_circ_29307,RMVar_hsa_circ_205839,RMVar_hsa_circ_361803,RMVar_hsa_circ_353783,RMVar_hsa_circ_315007,RMVar_hsa_circ_72876,RMVar_hsa_circ_338147,RMVar_hsa_circ_68354,RMVar_hsa_circ_205849,RMVar_hsa_circ_205850,RMVar_hsa_circ_357938,RMVar_hsa_circ_326401,RMVar_hsa_circ_205856,RMVar_hsa_circ_22887,RMVar_hsa_circ_62352,RMVar_hsa_circ_205854,RMVar_hsa_circ_317578,RMVar_hsa_circ_322130,RMVar_hsa_circ_292812,RMVar_hsa_circ_363527 28316 RMVar_ID_28316 Human_SNP_ID_109069457 A-to-I Human chr2 - 200977594 200977594 200977594 CACCCACCTGGCCTCCCAGAAGTGCTAGGATTACAGACATAACTACCACACCTGGCCTGAAGATT CACCCACCTGGCCTCCCAGAAGTGCTAGGATTGCAGACATAACTACCACACCTGGCCTGAAGATT T C FAM126B Ensembl:ENSG00000155744 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1264511358 Functional Loss SNV dbSNP153 33..33 33 - - - 28317 RMVar_ID_28317 Human_SNP_ID_109069477 A-to-I Human chr2 - 200977678 200977678 200977678 CCTGGCTAATTTTTGTATTTTTAGTAGAGACGAGGTTTTGCCATGTTGCCCAGGCTGGTCTCGAA CCTGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTTGCCATGTTGCCCAGGCTGGTCTCGAA T C FAM126B Ensembl:ENSG00000155744 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1341340617 Functional Loss SNV dbSNP153 33..33 33 - - - 28318 RMVar_ID_28318 Human_SNP_ID_109069480 A-to-I Human chr2 - 200977685 200977685 200977685 CACCACACCTGGCTAATTTTTGTATTTTTAGTAGAGACGAGGTTTTGCCATGTTGCCCAGGCTGG CACCACACCTGGCTAATTTTTGTATTTTTAGTGGAGACGAGGTTTTGCCATGTTGCCCAGGCTGG T C FAM126B Ensembl:ENSG00000155744 Protein coding 3'UTR GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1382502160 Functional Loss SNV dbSNP153 33..33 33 - - - 28319 RMVar_ID_28319 Human_SNP_ID_109069503 A-to-I Human chr2 - 200977783 200977783 200977783 CAGTGGCACTATCACGGCTCACTGCAGCCTCAACCTCCCTGGGCTCAGGTGATCTTCCCACCTCA CAGTGGCACTATCACGGCTCACTGCAGCCTCAGCCTCCCTGGGCTCAGGTGATCTTCCCACCTCA T C FAM126B Ensembl:ENSG00000155744 Protein coding 3'UTR GSE100210;GSE107867 HepG2 cell line;ASD brains,cerebellum - 29129909,30559470 RNA-Seq:(High) rs916792159 Functional Loss SNV dbSNP153 33..33 33 - - - 28320 RMVar_ID_28320 Human_SNP_ID_109070940 A-to-I Human chr2 - 200984178 200984178 200984178 AAAATTAGCCAAGCATGGTGGCAGATGCCTGTAGTCCCAGCTGCTTAAGAGGCTGAGGTGGGAGG AAAATTAGCCAAGCATGGTGGCAGATGCCTGTGGTCCCAGCTGCTTAAGAGGCTGAGGTGGGAGG T C FAM126B Ensembl:ENSG00000155744 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1468922160 Functional Loss SNV dbSNP153 33..33 33 - - - 28321 RMVar_ID_28321 Human_SNP_ID_109073153 A-to-I Human chr2 - 200994783 200994783 200994783 TTGTCCAGGCTGGTCTTGAACTCCTGGCCTCAAGTGATCTTCCTACCTTGGTCTCCCAGAGTACT TTGTCCAGGCTGGTCTTGAACTCCTGGCCTCACGTGATCTTCCTACCTTGGTCTCCCAGAGTACT T G FAM126B Ensembl:ENSG00000155744 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs887549472 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22681,RMVar_hsa_circ_266309,RMVar_hsa_circ_342207,RMVar_hsa_circ_324559,RMVar_hsa_circ_266188,RMVar_hsa_circ_26728,RMVar_hsa_circ_50991,RMVar_hsa_circ_289864,RMVar_hsa_circ_336646,RMVar_hsa_circ_341601,RMVar_hsa_circ_71860,RMVar_hsa_circ_205859,RMVar_hsa_circ_205860,RMVar_hsa_circ_61759 28322 RMVar_ID_28322 Human_SNP_ID_109073507 A-to-I Human chr2 - 200996445 200996445 200996445 TTTTTTTTTTTTAAAAGAGACCAGGTTTCACAATGTTGCACAGGCAGGTCACAAACTCCTGGGAT TTTTTTTTTTTTAAAAGAGACCAGGTTTCACAGTGTTGCACAGGCAGGTCACAAACTCCTGGGAT T C FAM126B Ensembl:ENSG00000155744 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1001031229 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22681,RMVar_hsa_circ_266309,RMVar_hsa_circ_342207,RMVar_hsa_circ_324559,RMVar_hsa_circ_266188,RMVar_hsa_circ_26728,RMVar_hsa_circ_50991,RMVar_hsa_circ_289864,RMVar_hsa_circ_336646,RMVar_hsa_circ_341601,RMVar_hsa_circ_71860,RMVar_hsa_circ_205859,RMVar_hsa_circ_205860,RMVar_hsa_circ_61759 28323 RMVar_ID_28323 Human_SNP_ID_109073536 A-to-I Human chr2 - 200996603 200996603 200996603 TGGACAGACCTAGGCTTAAATCTTGTTCTGTCACCCAGACTGGAGTGCAGTGGTGCCATATTGGC TGGACAGACCTAGGCTTAAATCTTGTTCTGTCGCCCAGACTGGAGTGCAGTGGTGCCATATTGGC T C FAM126B Ensembl:ENSG00000155744 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1244103243 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22681,RMVar_hsa_circ_266309,RMVar_hsa_circ_342207,RMVar_hsa_circ_324559,RMVar_hsa_circ_266188,RMVar_hsa_circ_26728,RMVar_hsa_circ_50991,RMVar_hsa_circ_289864,RMVar_hsa_circ_336646,RMVar_hsa_circ_341601,RMVar_hsa_circ_71860,RMVar_hsa_circ_205859,RMVar_hsa_circ_205860,RMVar_hsa_circ_61759 28324 RMVar_ID_28324 Human_SNP_ID_109075053 A-to-I Human chr2 - 201003203 201003203 201003203 TAAAAAATAGCTGAGTGTGGTGATACATGCCTATGGTCCTAGGTACTCTGGAGGCCGAGGCTGGA TAAAAAATAGCTGAGTGTGGTGATACATGCCTGTGGTCCTAGGTACTCTGGAGGCCGAGGCTGGA T C FAM126B Ensembl:ENSG00000155744 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs997358858 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13737418 RMVar_hsa_circ_22681,RMVar_hsa_circ_266309,RMVar_hsa_circ_342207,RMVar_hsa_circ_324559,RMVar_hsa_circ_26728,RMVar_hsa_circ_10126,RMVar_hsa_circ_50991,RMVar_hsa_circ_289864,RMVar_hsa_circ_336646,RMVar_hsa_circ_71860,RMVar_hsa_circ_205859,RMVar_hsa_circ_205860,RMVar_hsa_circ_339190,RMVar_hsa_circ_61759,RMVar_hsa_circ_363773,RMVar_hsa_circ_284295,RMVar_hsa_circ_205861 28325 RMVar_ID_28325 Human_SNP_ID_109076554 A-to-I Human chr2 - 201009584 201009584 201009584 GTGGTAGTGGGTACCTGTAATGCCAGCTACTCAGGTGTCTGAGGCACAGGAATCACTCAAACCCA GTGGTAGTGGGTACCTGTAATGCCAGCTACTCGGGTGTCTGAGGCACAGGAATCACTCAAACCCA T C FAM126B Ensembl:ENSG00000155744 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1365969613 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_205863,RMVar_hsa_circ_22681,RMVar_hsa_circ_266309,RMVar_hsa_circ_342207,RMVar_hsa_circ_324559,RMVar_hsa_circ_10126,RMVar_hsa_circ_50991,RMVar_hsa_circ_289864,RMVar_hsa_circ_336646,RMVar_hsa_circ_71860,RMVar_hsa_circ_205859,RMVar_hsa_circ_205860,RMVar_hsa_circ_339190,RMVar_hsa_circ_61759,RMVar_hsa_circ_363773,RMVar_hsa_circ_284295,RMVar_hsa_circ_294531,RMVar_hsa_circ_313376,RMVar_hsa_circ_205861,RMVar_hsa_circ_328625,RMVar_hsa_circ_297510,RMVar_hsa_circ_46301,RMVar_hsa_circ_283908,RMVar_hsa_circ_205865,RMVar_hsa_circ_205866,RMVar_hsa_circ_205864,RMVar_hsa_circ_205862 28326 RMVar_ID_28326 Human_SNP_ID_109076632 A-to-I Human chr2 - 201009914 201009914 201009914 TATTTTTAGTGCAGATGGGGTTTCACTGTGTTAGCCAGGATGGTCTTGATATCCTGACCTCTTGA TATTTTTAGTGCAGATGGGGTTTCACTGTGTTGGCCAGGATGGTCTTGATATCCTGACCTCTTGA T C FAM126B Ensembl:ENSG00000155744 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs960098219 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_205863,RMVar_hsa_circ_22681,RMVar_hsa_circ_266309,RMVar_hsa_circ_342207,RMVar_hsa_circ_324559,RMVar_hsa_circ_10126,RMVar_hsa_circ_50991,RMVar_hsa_circ_289864,RMVar_hsa_circ_336646,RMVar_hsa_circ_71860,RMVar_hsa_circ_205859,RMVar_hsa_circ_205860,RMVar_hsa_circ_339190,RMVar_hsa_circ_61759,RMVar_hsa_circ_363773,RMVar_hsa_circ_284295,RMVar_hsa_circ_294531,RMVar_hsa_circ_313376,RMVar_hsa_circ_205861,RMVar_hsa_circ_328625,RMVar_hsa_circ_297510,RMVar_hsa_circ_46301,RMVar_hsa_circ_283908,RMVar_hsa_circ_205865,RMVar_hsa_circ_205866,RMVar_hsa_circ_205864,RMVar_hsa_circ_205862 28327 RMVar_ID_28327 Human_SNP_ID_109076662 A-to-I Human chr2 - 201009982 201009982 201009982 CTCCTGTCTCAGCCTTCCGAGTAGCTGGGACTACAGGTGCATGCCACCACGCCCGGCTAATTTTT CTCCTGTCTCAGCCTTCCGAGTAGCTGGGACTGCAGGTGCATGCCACCACGCCCGGCTAATTTTT T C FAM126B Ensembl:ENSG00000155744 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1298158268 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_205863,RMVar_hsa_circ_22681,RMVar_hsa_circ_266309,RMVar_hsa_circ_342207,RMVar_hsa_circ_324559,RMVar_hsa_circ_10126,RMVar_hsa_circ_50991,RMVar_hsa_circ_289864,RMVar_hsa_circ_336646,RMVar_hsa_circ_71860,RMVar_hsa_circ_205859,RMVar_hsa_circ_205860,RMVar_hsa_circ_339190,RMVar_hsa_circ_61759,RMVar_hsa_circ_363773,RMVar_hsa_circ_284295,RMVar_hsa_circ_294531,RMVar_hsa_circ_313376,RMVar_hsa_circ_205861,RMVar_hsa_circ_328625,RMVar_hsa_circ_297510,RMVar_hsa_circ_46301,RMVar_hsa_circ_283908,RMVar_hsa_circ_205865,RMVar_hsa_circ_205866,RMVar_hsa_circ_205864,RMVar_hsa_circ_205862 28328 RMVar_ID_28328 Human_SNP_ID_109079972 A-to-I Human chr2 - 201025082 201025082 201025082 TTGAGACAGAGTCTCACTCTGTTGCCTAGGCTAGAGTGCAGTGGTGTGAACATGGCTCAGTGCAG TTGAGACAGAGTCTCACTCTGTTGCCTAGGCTGGAGTGCAGTGGTGTGAACATGGCTCAGTGCAG T C FAM126B Ensembl:ENSG00000155744 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1160578725 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_342207,RMVar_hsa_circ_10126,RMVar_hsa_circ_71860,RMVar_hsa_circ_313376,RMVar_hsa_circ_37633,RMVar_hsa_circ_205862,RMVar_hsa_circ_308516,RMVar_hsa_circ_205870,RMVar_hsa_circ_369095,RMVar_hsa_circ_340774,RMVar_hsa_circ_205873 28329 RMVar_ID_28329 Human_SNP_ID_109081395 A-to-I Human chr2 - 201030707 201030707 201030707 GGGTGTGGTGGTGCACTCCTGGAATCCCAGCTACTTGGGAGGCCGAGGCAGGAGAATCACTTGAA GGGTGTGGTGGTGCACTCCTGGAATCCCAGCTGCTTGGGAGGCCGAGGCAGGAGAATCACTTGAA T C FAM126B Ensembl:ENSG00000155744 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1057021944 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_342207,RMVar_hsa_circ_10126,RMVar_hsa_circ_71860,RMVar_hsa_circ_313376,RMVar_hsa_circ_37633,RMVar_hsa_circ_205862,RMVar_hsa_circ_308516,RMVar_hsa_circ_205870,RMVar_hsa_circ_369095,RMVar_hsa_circ_340774,RMVar_hsa_circ_205873 28330 RMVar_ID_28330 Human_SNP_ID_109086462 A-to-I Human chr2 - 201049989 201049989 201049989 ATAATTTAGGAATGTAGTTTTAGGCCAGGTGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGC ATAATTTAGGAATGTAGTTTTAGGCCAGGTGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGC T C FAM126B Ensembl:ENSG00000155744 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1481313164 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13737781 RMVar_hsa_circ_37633,RMVar_hsa_circ_342800,RMVar_hsa_circ_205874 28331 RMVar_ID_28331 Human_SNP_ID_109087223 A-to-I Human chr2 - 201053157 201053156 201053158 GATTGCGCCATTGTGCTCCAGCCTGGTTGACAAGAGCGAAATTCCGTCTCAAAAAAAAAAAAATT GATTGCGCCATTGTGCTCCAGCCTGGTTGAC__GAGCGAAATTCCGTCTCAAAAAAAAAAAAATT CTT C FAM126B Ensembl:ENSG00000155744 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1160931834 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_37633,RMVar_hsa_circ_342800,RMVar_hsa_circ_205874 28332 RMVar_ID_28332 Human_SNP_ID_109091967 A-to-I Human chr2 + 201073519 201073519 201073519 GGCTGGGCACGGTGGCTCACGCCTGTAATCCCAACACTTTGGGTGGCCGAGGCAGGCGGATAATG GGCTGGGCACGGTGGCTCACGCCTGTAATCCCGACACTTTGGGTGGCCGAGGCAGGCGGATAATG A G NDUFB3 Ensembl:ENSG00000119013 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1167079880 Functional Loss SNV dbSNP153 33..33 33 - - - 28333 RMVar_ID_28333 Human_SNP_ID_109094597 A-to-I Human chr2 + 201084167 201084167 201084167 AAAAAATTAGCTGGATGTGGTGGTGTGCGCCTATAATCCCAGCTACTGGGGAGGCTGAGGCAGGA AAAAAATTAGCTGGATGTGGTGGTGTGCGCCTGTAATCCCAGCTACTGGGGAGGCTGAGGCAGGA A G NDUFB3 Ensembl:ENSG00000119013 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs903018486 Functional Loss SNV dbSNP153 33..33 33 - - - 28334 RMVar_ID_28334 Human_SNP_ID_109095787 A-to-I Human chr2 - 201089283 201089283 201089283 CAGGTCACTCTAGCCTCGACCTCCTGGGCCCAAGCAATCCTCCTGCCTCAGCTTCCTGAGTAGCT CAGGTCACTCTAGCCTCGACCTCCTGGGCCCAGGCAATCCTCCTGCCTCAGCTTCCTGAGTAGCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs896686387 Functional Loss SNV dbSNP153 33..33 33 - - - 28335 RMVar_ID_28335 Human_SNP_ID_109098767 A-to-I Human chr2 - 201100813 201100813 201100813 CTCACTGTAGCCTCGATCTCCTAGACTCAAGCAGTCCTCCTACCTCAGCTTCCTAAGTAGCTAGT CTCACTGTAGCCTCGATCTCCTAGACTCAAGCGGTCCTCCTACCTCAGCTTCCTAAGTAGCTAGT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935525896 Functional Loss SNV dbSNP153 33..33 33 - - - 28336 RMVar_ID_28336 Human_SNP_ID_109101537 A-to-I Human chr2 - 201113915 201113915 201113915 GCCTCAAGTGATCTTCCTGCCTAGGTCTTCCAAAGCACTGGGATTACAGGCATGACCACTGCTGC GCCTCAAGTGATCTTCCTGCCTAGGTCTTCCAGAGCACTGGGATTACAGGCATGACCACTGCTGC T C lnc-FAM126B-1,lnc-FAM126B-1:2 RNACentral:URS00008BC19C,RNACentral:URS00009AE1E0 lincRNA,lincRNA exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1258480722 Functional Loss SNV dbSNP153 33..33 33 - - - 28337 RMVar_ID_28337 Human_SNP_ID_109101842 A-to-I Human chr2 - 201114548 201114546 201114548 TCCAAGTTTGGTTTTTTGTTTGTTTTTGAGACAGGGTCTCACTCCAGGCTGGAGTGCAGTGACCC TCCAAGTTTGGTTTTTTGTTTGTTTTTGAGAC__GGTCTCACTCCAGGCTGGAGTGCAGTGACCC CCT C lnc-FAM126B-1,lnc-FAM126B-1:2 RNACentral:URS00008BC19C,RNACentral:URS00009AE1E0 lincRNA,lincRNA exon,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1320503908 Functional Loss DEL dbSNP153 33..34 33 - - - 28338 RMVar_ID_28338 Human_SNP_ID_109111443 A-to-I Human chr2 + 201155946 201155946 201155946 CATGTCTGGCTAACTTTGTTTTTTATAGAGACAGGGTCTTTTGCTGTATTTCCCAGGGCGGTCTT CATGTCTGGCTAACTTTGTTTTTTATAGAGACGGGGTCTTTTGCTGTATTTCCCAGGGCGGTCTT A G CFLAR Ensembl:ENSG00000003402 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1395042231 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58496,RMVar_hsa_circ_70596,RMVar_hsa_circ_205880,RMVar_hsa_circ_114505,RMVar_hsa_circ_205881,RMVar_hsa_circ_124592,RMVar_hsa_circ_319174,RMVar_hsa_circ_365058,RMVar_hsa_circ_205885 28339 RMVar_ID_28339 Human_SNP_ID_109113454 A-to-I Human chr2 + 201164010 201164010 201164010 CCAAAAGGCTGGGCGTAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGAGGGCAG CCAAAAGGCTGGGCGTAGTGGCTCACACCTGTGATCCCAGCACTTTGGGAGGCCAAGGAGGGCAG A G CFLAR Ensembl:ENSG00000003402 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1138209 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25499461 RMVar_hsa_circ_58496 28340 RMVar_ID_28340 Human_SNP_ID_109113461 A-to-I Human chr2 + 201164032 201164032 201164032 TCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGAGGGCAGATCACTTCAGGTCAGGAGTTCG TCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGAGGGCAGATCACTTCAGGTCAGGAGTTCG A G CFLAR Ensembl:ENSG00000003402 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs3201947 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58496 28341 RMVar_ID_28341 Human_SNP_ID_109113475 A-to-I Human chr2 + 201164087 201164087 201164087 CAGGAGTTCGAGACCAGCCTGGCCAACATGGTAAACGCTGTCCCTAGTAAAAATACAAAAATTAG CAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAACGCTGTCCCTAGTAAAAATACAAAAATTAG A G CFLAR Ensembl:ENSG00000003402 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1142190 Functional Loss SNV dbSNP153 33..33 33 - - - 28342 RMVar_ID_28342 Human_SNP_ID_109113482 A-to-I Human chr2 + 201164104 201164104 201164104 CCTGGCCAACATGGTAAACGCTGTCCCTAGTAAAAATACAAAAATTAGCTGGGTGTGGGTGTGGG CCTGGCCAACATGGTAAACGCTGTCCCTAGTAGAAATACAAAAATTAGCTGGGTGTGGGTGTGGG A G CFLAR Ensembl:ENSG00000003402 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1138250 Functional Loss SNV dbSNP153 33..33 33 - - - 28343 RMVar_ID_28343 Human_SNP_ID_109113483 A-to-I Human chr2 + 201164109 201164109 201164109 CCAACATGGTAAACGCTGTCCCTAGTAAAAATACAAAAATTAGCTGGGTGTGGGTGTGGGTACCT CCAACATGGTAAACGCTGTCCCTAGTAAAAATGCAAAAATTAGCTGGGTGTGGGTGTGGGTACCT A G CFLAR Ensembl:ENSG00000003402 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1138251 Functional Loss SNV dbSNP153 33..33 33 - - - 28344 RMVar_ID_28344 Human_SNP_ID_109113484 A-to-I Human chr2 + 201164111 201164111 201164111 AACATGGTAAACGCTGTCCCTAGTAAAAATACAAAAATTAGCTGGGTGTGGGTGTGGGTACCTGT AACATGGTAAACGCTGTCCCTAGTAAAAATACCAAAATTAGCTGGGTGTGGGTGTGGGTACCTGT A C CFLAR Ensembl:ENSG00000003402 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs2540451 Functional Loss SNV dbSNP153 33..33 33 - - - 28345 RMVar_ID_28345 Human_SNP_ID_109113491 A-to-I Human chr2 + 201164138 201164138 201164138 AATACAAAAATTAGCTGGGTGTGGGTGTGGGTACCTGTATTCCCAGTTACTTGGGAGGCTGAGGT AATACAAAAATTAGCTGGGTGTGGGTGTGGGTGCCTGTATTCCCAGTTACTTGGGAGGCTGAGGT A G CFLAR Ensembl:ENSG00000003402 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1142191 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9047 28346 RMVar_ID_28346 Human_SNP_ID_109113494 A-to-I Human chr2 + 201164144 201164144 201164144 AAAATTAGCTGGGTGTGGGTGTGGGTACCTGTATTCCCAGTTACTTGGGAGGCTGAGGTGGGAGG AAAATTAGCTGGGTGTGGGTGTGGGTACCTGTGTTCCCAGTTACTTGGGAGGCTGAGGTGGGAGG A G CFLAR Ensembl:ENSG00000003402 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1138258 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9048 28347 RMVar_ID_28347 Human_SNP_ID_109113496 A-to-I Human chr2 + 201164154 201164154 201164154 GGGTGTGGGTGTGGGTACCTGTATTCCCAGTTACTTGGGAGGCTGAGGTGGGAGGATCTTTTGAA GGGTGTGGGTGTGGGTACCTGTATTCCCAGTTGCTTGGGAGGCTGAGGTGGGAGGATCTTTTGAA A G CFLAR Ensembl:ENSG00000003402 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1142195 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9048 28348 RMVar_ID_28348 Human_SNP_ID_109113786 A-to-I Human chr2 + 201165410 201165410 201165410 CTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCTCCTGCCACCACACCCGGCTAATTTTT CTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTGCAGGCTCCTGCCACCACACCCGGCTAATTTTT A G CFLAR Ensembl:ENSG00000003402 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1349394974 Functional Loss SNV dbSNP153 33..33 33 - - - 28349 RMVar_ID_28349 Human_SNP_ID_109113793 A-to-I Human chr2 + 201165451 201165451 201165451 TGCCACCACACCCGGCTAATTTTTGTATTTTTAGTGGAGACAGGGTTTCCACCATGTTGGCCAGC TGCCACCACACCCGGCTAATTTTTGTATTTTTGGTGGAGACAGGGTTTCCACCATGTTGGCCAGC A G CFLAR Ensembl:ENSG00000003402 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1414193326 Functional Loss SNV dbSNP153 33..33 33 - - - 28350 RMVar_ID_28350 Human_SNP_ID_109113800 A-to-I Human chr2 + 201165481 201165481 201165481 TTAGTGGAGACAGGGTTTCCACCATGTTGGCCAGCGTGGTCTTGAACTCCTGACCTCAGGTGATT TTAGTGGAGACAGGGTTTCCACCATGTTGGCCGGCGTGGTCTTGAACTCCTGACCTCAGGTGATT A G CFLAR Ensembl:ENSG00000003402 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs906741208 Functional Loss SNV dbSNP153 33..33 33 - - - 28351 RMVar_ID_28351 Human_SNP_ID_109113811 A-to-I Human chr2 + 201165515 201165515 201165515 CGTGGTCTTGAACTCCTGACCTCAGGTGATTCACCAGCCTCGGCCTCCCAAAGTGCTGGGATTAC CGTGGTCTTGAACTCCTGACCTCAGGTGATTCGCCAGCCTCGGCCTCCCAAAGTGCTGGGATTAC A G CFLAR Ensembl:ENSG00000003402 Protein coding 3'UTR GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1301961617 Functional Loss SNV dbSNP153 33..33 33 - - - 28352 RMVar_ID_28352 Human_SNP_ID_109113821 A-to-I Human chr2 + 201165546 201165546 201165546 CACCAGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACTGCACCTGGCCTATTATT CACCAGCCTCGGCCTCCCAAAGTGCTGGGATTGCAGGTGTGAGCCACTGCACCTGGCCTATTATT A G CFLAR Ensembl:ENSG00000003402 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1181550194 Functional Loss SNV dbSNP153 33..33 33 - - - 28353 RMVar_ID_28353 Human_SNP_ID_109114352 A-to-I Human chr2 + 201166842 201166842 201166842 TACGAAAACCAGTCAGGCGTGGCGGCGCCCGCAATGGCAGGCACGCGGCAGGCCGAGGCGGGAGA TACGAAAACCAGTCAGGCGTGGCGGCGCCCGCGATGGCAGGCACGCGGCAGGCCGAGGCGGGAGA A G CFLAR Ensembl:ENSG00000003402 Protein coding 3'UTR GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 29129909,30559470 RNA-Seq:(High) rs904923599 Functional Loss SNV dbSNP153 33..33 33 - - - 28354 RMVar_ID_28354 Human_SNP_ID_109114353 A-to-I Human chr2 + 201166842 201166842 201166842 TACGAAAACCAGTCAGGCGTGGCGGCGCCCGCAATGGCAGGCACGCGGCAGGCCGAGGCGGGAGA TACGAAAACCAGTCAGGCGTGGCGGCGCCCGCTATGGCAGGCACGCGGCAGGCCGAGGCGGGAGA A T CFLAR Ensembl:ENSG00000003402 Protein coding 3'UTR GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 29129909,30559470 RNA-Seq:(High) rs904923599 Functional Loss SNV dbSNP153 33..33 33 - - - 28355 RMVar_ID_28355 Human_SNP_ID_109114750 A-to-I Human chr2 + 201168079 201168078 201168079 TCCTGGCTAACATGTAAAACCCCGTCTCTACTAAAAATACAAAAAATTAGCCAGGCGTTGTGGCG TCCTGGCTAACATGTAAAACCCCGTCTCTACT_AAAATACAAAAAATTAGCCAGGCGTTGTGGCG TA T CFLAR Ensembl:ENSG00000003402 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1299869417 Functional Loss DEL dbSNP153 33..33 33 - - - 28356 RMVar_ID_28356 Human_SNP_ID_109116619 A-to-I Human chr2 + 201175894 201175894 201175894 GGGAGGCTGAGGCAGGTGGATTACTTGAGGTCAGTAGTTCGAGACCAGCCTGGCCATCATGATGA GGGAGGCTGAGGCAGGTGGATTACTTGAGGTCGGTAGTTCGAGACCAGCCTGGCCATCATGATGA A G CFLAR Ensembl:ENSG00000003402 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs541365312 Functional Loss SNV dbSNP153 33..33 33 - - - 28357 RMVar_ID_28357 Human_SNP_ID_109124071 A-to-I Human chr2 + 201206696 201206696 201206696 GTTGCCCAGGCTTGTCCTGAACTCTCAGGCTCAAGGAATTCTCCTGCCTCAGCCACCCAAGTACC GTTGCCCAGGCTTGTCCTGAACTCTCAGGCTCGAGGAATTCTCCTGCCTCAGCCACCCAAGTACC A G CASP10 Ensembl:ENSG00000003400 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1363212680 Functional Loss SNV dbSNP153 33..33 33 - - - 28358 RMVar_ID_28358 Human_SNP_ID_109127047 A-to-I Human chr2 + 201219149 201219149 201219149 AAAATTAGCCAGGTGTGGCGGCGAGCACCTGTAATCCCAGCTACTCGGGAGGCTGAGACAGGAGA AAAATTAGCCAGGTGTGGCGGCGAGCACCTGTTATCCCAGCTACTCGGGAGGCTGAGACAGGAGA A T CASP10 Ensembl:ENSG00000003400 Protein coding 3'UTR GSE47997;GSE38233;GSE38233;GSE100210;GSE100210 K562 cells&HepG2 cells;cultured B-cells;cultured B-cells;HepG2 cell line;HepG2 cell line - 23474544,24183664,24183664,29129909,29129909 RNA-Seq:(High) rs781583519 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26478944 28359 RMVar_ID_28359 Human_SNP_ID_109127049 A-to-I Human chr2 + 201219155 201219155 201219155 AGCCAGGTGTGGCGGCGAGCACCTGTAATCCCAGCTACTCGGGAGGCTGAGACAGGAGAATCTCT AGCCAGGTGTGGCGGCGAGCACCTGTAATCCCGGCTACTCGGGAGGCTGAGACAGGAGAATCTCT A G CASP10 Ensembl:ENSG00000003400 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1448017413 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26478944 28360 RMVar_ID_28360 Human_SNP_ID_109127057 A-to-I Human chr2 + 201219190 201219190 201219190 TACTCGGGAGGCTGAGACAGGAGAATCTCTTGAATCCAGGAGGCAGAGGCTGTGGTGAGCCAAGA TACTCGGGAGGCTGAGACAGGAGAATCTCTTGGATCCAGGAGGCAGAGGCTGTGGTGAGCCAAGA A G CASP10 Ensembl:ENSG00000003400 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1260511649 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26487565 28361 RMVar_ID_28361 Human_SNP_ID_109140837 A-to-I Human chr2 - 201278735 201278735 201278735 CTGAGGTCAGGAGTTCAAGAACAGCCTGACCAACATGGTGAAACCCCATCTCTACTAAATACAAT CTGAGGTCAGGAGTTCAAGAACAGCCTGACCAGCATGGTGAAACCCCATCTCTACTAAATACAAT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474594955 Functional Loss SNV dbSNP153 33..33 33 - - - 28362 RMVar_ID_28362 Human_SNP_ID_109143176 A-to-I Human chr2 + 201286639 201286639 201286639 GTTTGTTTTGTTTTGTTTTGTTTTTTTGAGACAGAATCTCGCTCTGTCGCCCAGGCTGGAGTGCA GTTTGTTTTGTTTTGTTTTGTTTTTTTGAGACGGAATCTCGCTCTGTCGCCCAGGCTGGAGTGCA A G CASP8 Ensembl:ENSG00000064012 Protein coding 3'UTR GSE38233;GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,32596459,32596459 RNA-Seq:(High) rs1472140233 Functional Loss SNV dbSNP153 33..33 33 - - - 28363 RMVar_ID_28363 Human_SNP_ID_109143344 A-to-I Human chr2 + 201287300 201287300 201287300 CATGTCTATAATCCCAGCACTTTGGGAGGTTGAGGTGGGAGGATTGCTTGAACCCAAGAGGTCAA CATGTCTATAATCCCAGCACTTTGGGAGGTTGGGGTGGGAGGATTGCTTGAACCCAAGAGGTCAA A G CASP8 Ensembl:ENSG00000064012 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs11551927 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26487570 28364 RMVar_ID_28364 Human_SNP_ID_109143354 A-to-I Human chr2 + 201287355 201287355 201287355 AAGAGGTCAAGGCTGCAGTGAGCCATGTTCACACCGCTGCACTCAAGCTTGGGTGACAGAACAAG AAGAGGTCAAGGCTGCAGTGAGCCATGTTCACGCCGCTGCACTCAAGCTTGGGTGACAGAACAAG A G CASP8 Ensembl:ENSG00000064012 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1006983924 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26478953 28365 RMVar_ID_28365 Human_SNP_ID_109143367 A-to-I Human chr2 + 201287385 201287385 201287385 ACACCGCTGCACTCAAGCTTGGGTGACAGAACAAGACCCCGTCTCAAAAAAAATTTTTTTTTTAA ACACCGCTGCACTCAAGCTTGGGTGACAGAACGAGACCCCGTCTCAAAAAAAATTTTTTTTTTAA A G CASP8 Ensembl:ENSG00000064012 Protein coding 3'UTR GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-Seq:(High) rs1045501 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26487571 Human_miRNA_ID_474595,Human_miRNA_ID_1133399,Human_miRNA_ID_1265486 28366 RMVar_ID_28366 Human_SNP_ID_109167767 A-to-I Human chr2 - 201395382 201395382 201395382 CTGAAGAATTGTCAGGGAAGAGTGATGAGCTGATTCGATACCAAGAAGAGCTTTCCTCTCTTTTG CTGAAGAATTGTCAGGGAAGAGTGATGAGCTGGTTCGATACCAAGAAGAGCTTTCCTCTCTTTTG T C TRAK2 Ensembl:ENSG00000115993 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs17857239 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1582233,Human_RBP_ID_1907537,Human_RBP_ID_18752673,Human_RBP_ID_19002819 Human_Splice_Rec_345926,Human_Splice_Rec_345927,Human_Splice_Rec_345956 RMVar_hsa_circ_4751,RMVar_hsa_circ_17914,RMVar_hsa_circ_94151,RMVar_hsa_circ_115027,RMVar_hsa_circ_124257,RMVar_hsa_circ_110821,RMVar_hsa_circ_205894,RMVar_hsa_circ_205895,RMVar_hsa_circ_205896,RMVar_hsa_circ_205897,RMVar_hsa_circ_205898,RMVar_hsa_circ_205901,RMVar_hsa_circ_60909,RMVar_hsa_circ_19003,RMVar_hsa_circ_347894,RMVar_hsa_circ_6282,RMVar_hsa_circ_41999,RMVar_hsa_circ_1769,RMVar_hsa_circ_205903 28367 RMVar_ID_28367 Human_SNP_ID_109171390 A-to-I Human chr2 + 201412454 201412454 201412454 AGGTATATTTATAAGTGAACTAGATCCTAAATAACTCAACTGATCCAACTGCCTACTGAAACTCT AGGTATATTTATAAGTGAACTAGATCCTAAATCACTCAACTGATCCAACTGCCTACTGAAACTCT A C STRADB Ensembl:ENSG00000082146 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs527788528 Functional Loss SNV dbSNP153 33..33 33 - - - 28368 RMVar_ID_28368 Human_SNP_ID_109179869 A-to-I Human chr2 - 201450882 201450882 201450882 ATTGATTTTGAGCCAGATGCCACATATCTTGAAAAAGAAAAACGGCTGACTTTAGTTTGAAGCGT ATTGATTTTGAGCCAGATGCCACATATCTTGAGAAAGAAAAACGGCTGACTTTAGTTTGAAGCGT T C TRAK2 Ensembl:ENSG00000115993 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs151230212 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94151,RMVar_hsa_circ_205896 28369 RMVar_ID_28369 Human_SNP_ID_109187964 A-to-I Human chr2 - 201487611 201487611 201487611 TGCGGCCAAAAAAAATTAAAAGAGGATATTGAAAAATGTTCGCTCATTTGTGATATTATAAAACA TGCGGCCAAAAAAAATTAAAAGAGGATATTGAGAAATGTTCGCTCATTTGTGATATTATAAAACA T C C2CD6 Ensembl:ENSG00000155754 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs754205386 Functional Loss SNV dbSNP153 33..33 33 - - - 28370 RMVar_ID_28370 Human_SNP_ID_109225268 A-to-I Human chr2 - 201648907 201648907 201648907 AGCACAAGCCACCATGCCTGGTTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCGCCATGTTTG AGCACAAGCCACCATGCCTGGTTAATTTTTGTGTTTTTAGTAGAGACAGGGTTTCGCCATGTTTG T C MPP4 Ensembl:ENSG00000082126 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1480670775 Functional Loss SNV dbSNP153 33..33 33 - - - 28371 RMVar_ID_28371 Human_SNP_ID_109225284 A-to-I Human chr2 - 201648982 201648982 201648982 TCCGCTCACTGCAACCTCCGCTTCCCGGGTTCAAGCAATTCTCGTGCCTCAGCCTCCCGAGTAGC TCCGCTCACTGCAACCTCCGCTTCCCGGGTTCGAGCAATTCTCGTGCCTCAGCCTCCCGAGTAGC T C MPP4 Ensembl:ENSG00000082126 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1037131940 Functional Loss SNV dbSNP153 33..33 33 - - - 28372 RMVar_ID_28372 Human_SNP_ID_109255695 A-to-I Human chr2 - 201775223 201775223 201775223 AAAAAGGAAGTGTTAATGGCTACATGAAATCTATGGTAATTTTGTATCCAAGTCACTCAATGTCT AAAAAGGAAGTGTTAATGGCTACATGAAATCTGTGGTAATTTTGTATCCAAGTCACTCAATGTCT T C ALS2 Ensembl:ENSG00000003393 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1295193510 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_205931,RMVar_hsa_circ_111652 28373 RMVar_ID_28373 Human_SNP_ID_109256113 A-to-I Human chr2 - 201777157 201777155 201777158 CTCTGGAAGTATAGGGGAGCAAGTTGTATAATAAGGCCCTCAAAGGAATTTGGACATGTTGTGAC CTCTGGAAGTATAGGGGAGCAAGTTGTATAA___GGCCCTCAAAGGAATTTGGACATGTTGTGAC CTTA C ALS2 Ensembl:ENSG00000003393 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1224961117 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_205931,RMVar_hsa_circ_111652 28374 RMVar_ID_28374 Human_SNP_ID_109357239 A-to-I Human chr2 - 202207765 202207765 202207765 TGCTGAGGTTGCAGTGAGCTGAGGTTGAGCCCAGGAGGCTGAGGTTGCAGTGAGCTGAGATTGTG TGCTGAGGTTGCAGTGAGCTGAGGTTGAGCCCCGGAGGCTGAGGTTGCAGTGAGCTGAGATTGTG T G SUMO1 Ensembl:ENSG00000116030 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1436796352 Functional Loss SNV dbSNP153 33..33 33 - - - 28375 RMVar_ID_28375 Human_SNP_ID_109357307 A-to-I Human chr2 - 202207981 202207981 202207981 TTTTTGGTCAGGCACAGTGGCCCACGCCTGCAATCCTAGCACTTTGGGAGGCTGAGGCGGGCTGG TTTTTGGTCAGGCACAGTGGCCCACGCCTGCAGTCCTAGCACTTTGGGAGGCTGAGGCGGGCTGG T C SUMO1 Ensembl:ENSG00000116030 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1248073772 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_347258 28376 RMVar_ID_28376 Human_SNP_ID_109358307 A-to-I Human chr2 - 202212060 202212060 202212060 ACCTCCTGGACTCAAGTGATTCCCAATGCCTCAGTCTCCCGAGTAGCTGGGATTACAGGCACCTG ACCTCCTGGACTCAAGTGATTCCCAATGCCTCCGTCTCCCGAGTAGCTGGGATTACAGGCACCTG T G SUMO1 Ensembl:ENSG00000116030 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1365771474 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13740055,Human_RBP_ID_25500015 RMVar_hsa_circ_51554,RMVar_hsa_circ_330911,RMVar_hsa_circ_48805 28377 RMVar_ID_28377 Human_SNP_ID_109361238 A-to-I Human chr2 - 202223440 202223440 202223440 GTGGTGGCACGCACCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAATCTG GTGGTGGCACGCACCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCTTGAATCTG T C SUMO1 Ensembl:ENSG00000116030 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1260037008 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48805 28378 RMVar_ID_28378 Human_SNP_ID_109361239 A-to-I Human chr2 - 202223448 202223447 202223448 AGCTGGGCGTGGTGGCACGCACCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATTGCT AGCTGGGCGTGGTGGCACGCACCTGTAATCCC_GCTACTCAGGAGGCTGAGGCAGGAGAATTGCT CT C SUMO1 Ensembl:ENSG00000116030 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1290529893 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_48805 28379 RMVar_ID_28379 Human_SNP_ID_109361242 A-to-I Human chr2 - 202223448 202223448 202223448 AGCTGGGCGTGGTGGCACGCACCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATTGCT AGCTGGGCGTGGTGGCACGCACCTGTAATCCCGGCTACTCAGGAGGCTGAGGCAGGAGAATTGCT T C SUMO1 Ensembl:ENSG00000116030 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1451628574 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48805 28380 RMVar_ID_28380 Human_SNP_ID_109361439 A-to-I Human chr2 - 202224130 202224130 202224130 GGGATTACAGGTGCCCGCCACTACGCCCGACTAACTTTTGTATTTTTAGTAGAGATGGGGTTTCA GGGATTACAGGTGCCCGCCACTACGCCCGACTGACTTTTGTATTTTTAGTAGAGATGGGGTTTCA T C SUMO1 Ensembl:ENSG00000116030 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1178566083 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48805 28381 RMVar_ID_28381 Human_SNP_ID_109361619 A-to-I Human chr2 - 202224728 202224728 202224728 ATAGAATTGTCATGGCTTATGCCTGTAATTCCAGCACTTTGGGAGGCTGAGATGGGAGGATTGCT ATAGAATTGTCATGGCTTATGCCTGTAATTCCGGCACTTTGGGAGGCTGAGATGGGAGGATTGCT T C SUMO1 Ensembl:ENSG00000116030 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs930394934 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48805 28382 RMVar_ID_28382 Human_SNP_ID_109364809 A-to-I Human chr2 - 202237317 202237317 202237317 CACTCACTGCACCCTCCCGCCTCCTGGGTTCAAGCAATTTTCGGGCCTCAGCCTCCCGAGTAGCT CACTCACTGCACCCTCCCGCCTCCTGGGTTCAGGCAATTTTCGGGCCTCAGCCTCCCGAGTAGCT T C SUMO1 Ensembl:ENSG00000116030 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749400873 Functional Loss SNV dbSNP153 33..33 33 - - - 28383 RMVar_ID_28383 Human_SNP_ID_109371808 A-to-I Human chr2 - 202263799 202263799 202263799 TTAAATTGCAACCTGCTGGGAGAATTGCTTGAACCCAGGAGGCGGAGGGTGCAGTGAGCCGAGGT TTAAATTGCAACCTGCTGGGAGAATTGCTTGACCCCAGGAGGCGGAGGGTGCAGTGAGCCGAGGT T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1486632684 Functional Loss SNV dbSNP153 33..33 33 - - - 28384 RMVar_ID_28384 Human_SNP_ID_109373348 A-to-I Human chr2 + 202268869 202268869 202268869 ACCTCAGGTGATCTGCCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCAC ACCTCAGGTGATCTGCCCGCCTCAGCCTCCCATAGTGCTGGGATTACAGGCGTGAGCCACTGCAC A T NOP58 Ensembl:ENSG00000055044 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs969206326 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93800,RMVar_hsa_circ_115742,RMVar_hsa_circ_205959,RMVar_hsa_circ_84262,RMVar_hsa_circ_205960,RMVar_hsa_circ_205958 28385 RMVar_ID_28385 Human_SNP_ID_109373552 A-to-I Human chr2 + 202269682 202269682 202269682 GACAATCAGTTGAACCTAGGAGCAGAGGTTGCAATGAGCTGCGGTCGCGCCACTGCAGTGCAGCC GACAATCAGTTGAACCTAGGAGCAGAGGTTGCCATGAGCTGCGGTCGCGCCACTGCAGTGCAGCC A C NOP58 Ensembl:ENSG00000055044 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1232995994 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4592605 RMVar_hsa_circ_93800,RMVar_hsa_circ_115742,RMVar_hsa_circ_205959,RMVar_hsa_circ_84262,RMVar_hsa_circ_205960,RMVar_hsa_circ_205958 28386 RMVar_ID_28386 Human_SNP_ID_109373981 A-to-I Human chr2 + 202271446 202271438 202271447 AAAATTAGCCAGGCATGGCAGCATGTGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGA AAAATTAGCCAGGCATGGCAGCATG_________TCCCAGCTACTTGGGAGGCTGAGGCAGGAGA GTGCCTGTAA G NOP58 Ensembl:ENSG00000055044 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1157950991 Functional Loss DEL dbSNP153 26..34 33 - - - RMVar_hsa_circ_93800,RMVar_hsa_circ_115742,RMVar_hsa_circ_205959,RMVar_hsa_circ_84262,RMVar_hsa_circ_205960,RMVar_hsa_circ_205958 28387 RMVar_ID_28387 Human_SNP_ID_109373985 A-to-I Human chr2 + 202271446 202271446 202271446 AAAATTAGCCAGGCATGGCAGCATGTGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGA AAAATTAGCCAGGCATGGCAGCATGTGCCTGTGATCCCAGCTACTTGGGAGGCTGAGGCAGGAGA A G NOP58 Ensembl:ENSG00000055044 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1242611118 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93800,RMVar_hsa_circ_115742,RMVar_hsa_circ_205959,RMVar_hsa_circ_84262,RMVar_hsa_circ_205960,RMVar_hsa_circ_205958 28388 RMVar_ID_28388 Human_SNP_ID_109374919 A-to-I Human chr2 + 202274655 202274655 202274655 GCAGTGGTGCACACCTGTAATCCCAGCTACTCAGGAGGCCGAGGCACTAGAATCTCATAAACCCA GCAGTGGTGCACACCTGTAATCCCAGCTACTCGGGAGGCCGAGGCACTAGAATCTCATAAACCCA A G NOP58 Ensembl:ENSG00000055044 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1205828047 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13740884 RMVar_hsa_circ_93800,RMVar_hsa_circ_115742,RMVar_hsa_circ_205959,RMVar_hsa_circ_84262,RMVar_hsa_circ_205960,RMVar_hsa_circ_205958 28389 RMVar_ID_28389 Human_SNP_ID_109375476 A-to-I Human chr2 + 202276686 202276686 202276686 ATATAGGAAAACCCCATCTCTACCAAAAACAAAAATTAGCTGGGTGTGGTGGTGCACACCTATAG ATATAGGAAAACCCCATCTCTACCAAAAACAACAATTAGCTGGGTGTGGTGGTGCACACCTATAG A C NOP58 Ensembl:ENSG00000055044 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1230401978 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17948016 RMVar_hsa_circ_14037,RMVar_hsa_circ_93800,RMVar_hsa_circ_115742,RMVar_hsa_circ_43257,RMVar_hsa_circ_205959,RMVar_hsa_circ_84262,RMVar_hsa_circ_205960,RMVar_hsa_circ_205958,RMVar_hsa_circ_375399,RMVar_hsa_circ_22997,RMVar_hsa_circ_205961 28390 RMVar_ID_28390 Human_SNP_ID_109376281 A-to-I Human chr2 + 202279642 202279642 202279642 CATGGTGAAACCTCGTCTCTACTGAAATTACAAAAATTAGCCGGGTGTGGTGGCACACACCTTAG CATGGTGAAACCTCGTCTCTACTGAAATTACACAAATTAGCCGGGTGTGGTGGCACACACCTTAG A C NOP58 Ensembl:ENSG00000055044 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs538828432 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13741068 RMVar_hsa_circ_14037,RMVar_hsa_circ_115742,RMVar_hsa_circ_43257,RMVar_hsa_circ_205959,RMVar_hsa_circ_84262,RMVar_hsa_circ_205960,RMVar_hsa_circ_19358,RMVar_hsa_circ_63084,RMVar_hsa_circ_331064,RMVar_hsa_circ_324431,RMVar_hsa_circ_291473,RMVar_hsa_circ_205962 28391 RMVar_ID_28391 Human_SNP_ID_109376282 A-to-I Human chr2 + 202279642 202279642 202279642 CATGGTGAAACCTCGTCTCTACTGAAATTACAAAAATTAGCCGGGTGTGGTGGCACACACCTTAG CATGGTGAAACCTCGTCTCTACTGAAATTACAGAAATTAGCCGGGTGTGGTGGCACACACCTTAG A G NOP58 Ensembl:ENSG00000055044 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs538828432 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13741068 RMVar_hsa_circ_14037,RMVar_hsa_circ_115742,RMVar_hsa_circ_43257,RMVar_hsa_circ_205959,RMVar_hsa_circ_84262,RMVar_hsa_circ_205960,RMVar_hsa_circ_19358,RMVar_hsa_circ_63084,RMVar_hsa_circ_331064,RMVar_hsa_circ_324431,RMVar_hsa_circ_291473,RMVar_hsa_circ_205962 28392 RMVar_ID_28392 Human_SNP_ID_109376293 A-to-I Human chr2 + 202279673 202279673 202279673 AAAAATTAGCCGGGTGTGGTGGCACACACCTTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAAATTAGCCGGGTGTGGTGGCACACACCTTGGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA A G NOP58 Ensembl:ENSG00000055044 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1240716080 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14037,RMVar_hsa_circ_115742,RMVar_hsa_circ_43257,RMVar_hsa_circ_205959,RMVar_hsa_circ_84262,RMVar_hsa_circ_205960,RMVar_hsa_circ_19358,RMVar_hsa_circ_63084,RMVar_hsa_circ_331064,RMVar_hsa_circ_324431,RMVar_hsa_circ_291473,RMVar_hsa_circ_205962 28393 RMVar_ID_28393 Human_SNP_ID_109376528 A-to-I Human chr2 + 202280606 202280606 202280606 CACCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAAGCATGAGCCACCGTGCCTGGCCATCATTT CACCCGCCTTGGCCTCCCAAAGTGCTGGGATTGCAAGCATGAGCCACCGTGCCTGGCCATCATTT A G NOP58 Ensembl:ENSG00000055044 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1559261852 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14037,RMVar_hsa_circ_115742,RMVar_hsa_circ_43257,RMVar_hsa_circ_205959,RMVar_hsa_circ_84262,RMVar_hsa_circ_205960,RMVar_hsa_circ_19358,RMVar_hsa_circ_63084,RMVar_hsa_circ_331064,RMVar_hsa_circ_324431,RMVar_hsa_circ_291473,RMVar_hsa_circ_205962 28394 RMVar_ID_28394 Human_SNP_ID_109376733 A-to-I Human chr2 + 202281292 202281292 202281292 AGGATTACAGGCGTGAGCCACCAGGGCCAGCTAATTTTTGTATTTTTAGTAGAGTGTTTCGTCAT AGGATTACAGGCGTGAGCCACCAGGGCCAGCTGATTTTTGTATTTTTAGTAGAGTGTTTCGTCAT A G NOP58 Ensembl:ENSG00000055044 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1425988673 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13741154 RMVar_hsa_circ_14037,RMVar_hsa_circ_115742,RMVar_hsa_circ_43257,RMVar_hsa_circ_205959,RMVar_hsa_circ_84262,RMVar_hsa_circ_205960,RMVar_hsa_circ_19358,RMVar_hsa_circ_63084,RMVar_hsa_circ_331064,RMVar_hsa_circ_324431,RMVar_hsa_circ_291473,RMVar_hsa_circ_205962 28395 RMVar_ID_28395 Human_SNP_ID_109376737 A-to-I Human chr2 + 202281310 202281309 202281311 CACCAGGGCCAGCTAATTTTTGTATTTTTAGTAGAGTGTTTCGTCATGTTAGCCAGGCTGGTCTC CACCAGGGCCAGCTAATTTTTGTATTTTTAGT__AGTGTTTCGTCATGTTAGCCAGGCTGGTCTC TAG T NOP58 Ensembl:ENSG00000055044 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1033749689 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_2614851,Human_RBP_ID_13741154,Human_RBP_ID_23182049 RMVar_hsa_circ_14037,RMVar_hsa_circ_115742,RMVar_hsa_circ_43257,RMVar_hsa_circ_205959,RMVar_hsa_circ_84262,RMVar_hsa_circ_205960,RMVar_hsa_circ_19358,RMVar_hsa_circ_63084,RMVar_hsa_circ_331064,RMVar_hsa_circ_324431,RMVar_hsa_circ_291473,RMVar_hsa_circ_205962 28396 RMVar_ID_28396 Human_SNP_ID_109377036 A-to-I Human chr2 - 202282474 202282474 202282474 CTAGCAGGCATGACCAAAAATATCGTGACTTTACCTTTATGACCCCTCCTAGTTTAGCATCAGCT CTAGCAGGCATGACCAAAAATATCGTGACTTTTCCTTTATGACCCCTCCTAGTTTAGCATCAGCT T A - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1397731568 Functional Loss SNV dbSNP153 33..33 33 - - - 28397 RMVar_ID_28397 Human_SNP_ID_109377304 A-to-I Human chr2 + 202283460 202283460 202283460 CCACGCCCAACCTGTAATTTTTTTTTTTTTTTAAGACGGAGTCTCACTCTGTCGCTAGGCTGAAG CCACGCCCAACCTGTAATTTTTTTTTTTTTTTTAGACGGAGTCTCACTCTGTCGCTAGGCTGAAG A T NOP58 Ensembl:ENSG00000055044 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1358509703 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23182050 RMVar_hsa_circ_14037,RMVar_hsa_circ_115742,RMVar_hsa_circ_43257,RMVar_hsa_circ_205959,RMVar_hsa_circ_84262,RMVar_hsa_circ_205960,RMVar_hsa_circ_51138,RMVar_hsa_circ_63084,RMVar_hsa_circ_331064,RMVar_hsa_circ_324431,RMVar_hsa_circ_125140,RMVar_hsa_circ_308746,RMVar_hsa_circ_334218,RMVar_hsa_circ_335529,RMVar_hsa_circ_277679,RMVar_hsa_circ_69947,RMVar_hsa_circ_205964,RMVar_hsa_circ_205965,RMVar_hsa_circ_205963 28398 RMVar_ID_28398 Human_SNP_ID_109377493 A-to-I Human chr2 + 202284126 202284125 202284127 CAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAATTAGCTGGGCATGGTGGCTCATGCCTG CAACATGGTGAAACCCCGTCTCTACTAAAAAT__AAAATTAGCTGGGCATGGTGGCTCATGCCTG TAC T NOP58 Ensembl:ENSG00000055044 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1302218151 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_14037,RMVar_hsa_circ_115742,RMVar_hsa_circ_43257,RMVar_hsa_circ_205959,RMVar_hsa_circ_84262,RMVar_hsa_circ_205960,RMVar_hsa_circ_51138,RMVar_hsa_circ_63084,RMVar_hsa_circ_331064,RMVar_hsa_circ_324431,RMVar_hsa_circ_125140,RMVar_hsa_circ_308746,RMVar_hsa_circ_334218,RMVar_hsa_circ_335529,RMVar_hsa_circ_277679,RMVar_hsa_circ_69947,RMVar_hsa_circ_205964,RMVar_hsa_circ_205965,RMVar_hsa_circ_205963 28399 RMVar_ID_28399 Human_SNP_ID_109377494 A-to-I Human chr2 + 202284126 202284126 202284126 CAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAATTAGCTGGGCATGGTGGCTCATGCCTG CAACATGGTGAAACCCCGTCTCTACTAAAAATGCAAAATTAGCTGGGCATGGTGGCTCATGCCTG A G NOP58 Ensembl:ENSG00000055044 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs931809724 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14037,RMVar_hsa_circ_115742,RMVar_hsa_circ_43257,RMVar_hsa_circ_205959,RMVar_hsa_circ_84262,RMVar_hsa_circ_205960,RMVar_hsa_circ_51138,RMVar_hsa_circ_63084,RMVar_hsa_circ_331064,RMVar_hsa_circ_324431,RMVar_hsa_circ_125140,RMVar_hsa_circ_308746,RMVar_hsa_circ_334218,RMVar_hsa_circ_335529,RMVar_hsa_circ_277679,RMVar_hsa_circ_69947,RMVar_hsa_circ_205964,RMVar_hsa_circ_205965,RMVar_hsa_circ_205963 28400 RMVar_ID_28400 Human_SNP_ID_109377810 A-to-I Human chr2 + 202285242 202285242 202285242 TTTTGTATTTTTAGTAGAGACGGGCTTTCACCATGTTGGCCTGGCTGATCTTGAACTCCTGACCT TTTTGTATTTTTAGTAGAGACGGGCTTTCACCGTGTTGGCCTGGCTGATCTTGAACTCCTGACCT A G NOP58 Ensembl:ENSG00000055044 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1331200212 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8509458,Human_RBP_ID_13741276,Human_RBP_ID_25500360 RMVar_hsa_circ_14037,RMVar_hsa_circ_115742,RMVar_hsa_circ_205960,RMVar_hsa_circ_51138,RMVar_hsa_circ_63084,RMVar_hsa_circ_331064,RMVar_hsa_circ_125140,RMVar_hsa_circ_334218,RMVar_hsa_circ_335529,RMVar_hsa_circ_277679,RMVar_hsa_circ_69947,RMVar_hsa_circ_276632,RMVar_hsa_circ_205964,RMVar_hsa_circ_205965,RMVar_hsa_circ_355556,RMVar_hsa_circ_205966 28401 RMVar_ID_28401 Human_SNP_ID_109377888 A-to-I Human chr2 + 202285423 202285423 202285423 CAGGCTGGGGTGCAGTGGTGCGATCTTGGCTCACTGCAACCTGGACATCCTGGACTCAAACAATG CAGGCTGGGGTGCAGTGGTGCGATCTTGGCTCGCTGCAACCTGGACATCCTGGACTCAAACAATG A G NOP58 Ensembl:ENSG00000055044 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs993386912 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2614874,Human_RBP_ID_6874175,Human_RBP_ID_8509459,Human_RBP_ID_13741282 RMVar_hsa_circ_14037,RMVar_hsa_circ_115742,RMVar_hsa_circ_205960,RMVar_hsa_circ_51138,RMVar_hsa_circ_63084,RMVar_hsa_circ_331064,RMVar_hsa_circ_125140,RMVar_hsa_circ_334218,RMVar_hsa_circ_335529,RMVar_hsa_circ_277679,RMVar_hsa_circ_69947,RMVar_hsa_circ_276632,RMVar_hsa_circ_205964,RMVar_hsa_circ_205965,RMVar_hsa_circ_355556,RMVar_hsa_circ_205966 28402 RMVar_ID_28402 Human_SNP_ID_109377927 A-to-I Human chr2 + 202285593 202285593 202285593 GAACTCCCAGGCTCAAGTGATCCACTTGCCTTAGCCTCCCAAAGTGCCGCGACTGCAGGGGTGAG GAACTCCCAGGCTCAAGTGATCCACTTGCCTTCGCCTCCCAAAGTGCCGCGACTGCAGGGGTGAG A C NOP58 Ensembl:ENSG00000055044 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,temporal_cortex - 29129909,30559470 RNA-Seq:(High) rs1346173652 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13741299,Human_RBP_ID_23848087 RMVar_hsa_circ_14037,RMVar_hsa_circ_115742,RMVar_hsa_circ_205960,RMVar_hsa_circ_51138,RMVar_hsa_circ_63084,RMVar_hsa_circ_331064,RMVar_hsa_circ_125140,RMVar_hsa_circ_334218,RMVar_hsa_circ_335529,RMVar_hsa_circ_277679,RMVar_hsa_circ_69947,RMVar_hsa_circ_276632,RMVar_hsa_circ_205964,RMVar_hsa_circ_205965,RMVar_hsa_circ_355556,RMVar_hsa_circ_205966 28403 RMVar_ID_28403 Human_SNP_ID_109378013 A-to-I Human chr2 + 202285939 202285939 202285939 ACTACAGGCTGGGCACGGTGGCTCACGCCTGTAATCCCAACACTTTGGGAGGCCAAGGCAGGCAG ACTACAGGCTGGGCACGGTGGCTCACGCCTGTCATCCCAACACTTTGGGAGGCCAAGGCAGGCAG A C NOP58 Ensembl:ENSG00000055044 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1026251533 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14037,RMVar_hsa_circ_115742,RMVar_hsa_circ_205960,RMVar_hsa_circ_51138,RMVar_hsa_circ_63084,RMVar_hsa_circ_331064,RMVar_hsa_circ_125140,RMVar_hsa_circ_334218,RMVar_hsa_circ_335529,RMVar_hsa_circ_277679,RMVar_hsa_circ_69947,RMVar_hsa_circ_276632,RMVar_hsa_circ_205964,RMVar_hsa_circ_205965,RMVar_hsa_circ_355556,RMVar_hsa_circ_205966 28404 RMVar_ID_28404 Human_SNP_ID_109378017 A-to-I Human chr2 + 202285945 202285945 202285945 GGCTGGGCACGGTGGCTCACGCCTGTAATCCCAACACTTTGGGAGGCCAAGGCAGGCAGATCACA GGCTGGGCACGGTGGCTCACGCCTGTAATCCCGACACTTTGGGAGGCCAAGGCAGGCAGATCACA A G NOP58 Ensembl:ENSG00000055044 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1559263383 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14037,RMVar_hsa_circ_115742,RMVar_hsa_circ_205960,RMVar_hsa_circ_51138,RMVar_hsa_circ_63084,RMVar_hsa_circ_331064,RMVar_hsa_circ_125140,RMVar_hsa_circ_334218,RMVar_hsa_circ_335529,RMVar_hsa_circ_277679,RMVar_hsa_circ_69947,RMVar_hsa_circ_276632,RMVar_hsa_circ_205964,RMVar_hsa_circ_205965,RMVar_hsa_circ_355556,RMVar_hsa_circ_205966 28405 RMVar_ID_28405 Human_SNP_ID_109378090 A-to-I Human chr2 + 202286170 202286170 202286170 CTCCACTGCAGTCCAGCCTGGGTGACAGAGTGAGACTCCATCTCAAAAAAAAAAAAAAAAAAGGG CTCCACTGCAGTCCAGCCTGGGTGACAGAGTGCGACTCCATCTCAAAAAAAAAAAAAAAAAAGGG A C NOP58 Ensembl:ENSG00000055044 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1321740193 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14037,RMVar_hsa_circ_115742,RMVar_hsa_circ_205960,RMVar_hsa_circ_51138,RMVar_hsa_circ_63084,RMVar_hsa_circ_331064,RMVar_hsa_circ_125140,RMVar_hsa_circ_334218,RMVar_hsa_circ_335529,RMVar_hsa_circ_277679,RMVar_hsa_circ_69947,RMVar_hsa_circ_276632,RMVar_hsa_circ_205964,RMVar_hsa_circ_205965,RMVar_hsa_circ_355556,RMVar_hsa_circ_205966 28406 RMVar_ID_28406 Human_SNP_ID_109378160 A-to-I Human chr2 + 202286321 202286321 202286321 GGTCAGGAGATCGAGACCATCCTGGTTAACACAGTGAAACCCCGTCTCTACTAAAAATACAAAAA GGTCAGGAGATCGAGACCATCCTGGTTAACACGGTGAAACCCCGTCTCTACTAAAAATACAAAAA A G NOP58 Ensembl:ENSG00000055044 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1195650694 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14037,RMVar_hsa_circ_115742,RMVar_hsa_circ_205960,RMVar_hsa_circ_51138,RMVar_hsa_circ_63084,RMVar_hsa_circ_331064,RMVar_hsa_circ_125140,RMVar_hsa_circ_334218,RMVar_hsa_circ_335529,RMVar_hsa_circ_277679,RMVar_hsa_circ_69947,RMVar_hsa_circ_276632,RMVar_hsa_circ_205964,RMVar_hsa_circ_205965,RMVar_hsa_circ_355556,RMVar_hsa_circ_205966 28407 RMVar_ID_28407 Human_SNP_ID_109378421 A-to-I Human chr2 + 202287243 202287243 202287243 GGCGTGCCCCACCATGCCTGGCTAATTTTTATATTTTTAGTAGAGACAGGGTTTCGCCATGTTGG GGCGTGCCCCACCATGCCTGGCTAATTTTTATGTTTTTAGTAGAGACAGGGTTTCGCCATGTTGG A G NOP58 Ensembl:ENSG00000055044 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs187028385 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14037,RMVar_hsa_circ_115742,RMVar_hsa_circ_205960,RMVar_hsa_circ_51138,RMVar_hsa_circ_63084,RMVar_hsa_circ_331064,RMVar_hsa_circ_125140,RMVar_hsa_circ_334218,RMVar_hsa_circ_335529,RMVar_hsa_circ_277679,RMVar_hsa_circ_69947,RMVar_hsa_circ_276632,RMVar_hsa_circ_205964,RMVar_hsa_circ_205965,RMVar_hsa_circ_355556,RMVar_hsa_circ_205966 28408 RMVar_ID_28408 Human_SNP_ID_109378630 A-to-I Human chr2 + 202287927 202287927 202287927 GAGGTCAGGAGTTCAAGACCAGCTTGGCCAACATGACAAAACTCTGTCTTTACTAAAAATACAAA GAGGTCAGGAGTTCAAGACCAGCTTGGCCAACGTGACAAAACTCTGTCTTTACTAAAAATACAAA A G NOP58 Ensembl:ENSG00000055044 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1031952876 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1582310 RMVar_hsa_circ_115742,RMVar_hsa_circ_205960,RMVar_hsa_circ_30972,RMVar_hsa_circ_51138,RMVar_hsa_circ_63084,RMVar_hsa_circ_331064,RMVar_hsa_circ_125140,RMVar_hsa_circ_334218,RMVar_hsa_circ_335529,RMVar_hsa_circ_69947,RMVar_hsa_circ_205965,RMVar_hsa_circ_355556,RMVar_hsa_circ_80453,RMVar_hsa_circ_358962,RMVar_hsa_circ_341238,RMVar_hsa_circ_60159,RMVar_hsa_circ_205967 28409 RMVar_ID_28409 Human_SNP_ID_109378631 A-to-I Human chr2 + 202287932 202287932 202287932 CAGGAGTTCAAGACCAGCTTGGCCAACATGACAAAACTCTGTCTTTACTAAAAATACAAAAAAAA CAGGAGTTCAAGACCAGCTTGGCCAACATGACCAAACTCTGTCTTTACTAAAAATACAAAAAAAA A C NOP58 Ensembl:ENSG00000055044 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1236811799 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1582310 RMVar_hsa_circ_115742,RMVar_hsa_circ_205960,RMVar_hsa_circ_30972,RMVar_hsa_circ_51138,RMVar_hsa_circ_63084,RMVar_hsa_circ_331064,RMVar_hsa_circ_125140,RMVar_hsa_circ_334218,RMVar_hsa_circ_335529,RMVar_hsa_circ_69947,RMVar_hsa_circ_205965,RMVar_hsa_circ_355556,RMVar_hsa_circ_80453,RMVar_hsa_circ_358962,RMVar_hsa_circ_341238,RMVar_hsa_circ_60159,RMVar_hsa_circ_205967 28410 RMVar_ID_28410 Human_SNP_ID_109379213 A-to-I Human chr2 + 202290130 202290130 202290130 GGTGTGCACCACCATGCCTGGCTAATTTTTGTATTTTTAATAGAGATGGGGTTTCACCATGTTGG GGTGTGCACCACCATGCCTGGCTAATTTTTGTGTTTTTAATAGAGATGGGGTTTCACCATGTTGG A G NOP58 Ensembl:ENSG00000055044 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1252126132 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115742,RMVar_hsa_circ_205960,RMVar_hsa_circ_30972,RMVar_hsa_circ_51138,RMVar_hsa_circ_63084,RMVar_hsa_circ_331064,RMVar_hsa_circ_125140,RMVar_hsa_circ_334218,RMVar_hsa_circ_335529,RMVar_hsa_circ_69947,RMVar_hsa_circ_205965,RMVar_hsa_circ_355556,RMVar_hsa_circ_80453,RMVar_hsa_circ_358962,RMVar_hsa_circ_341238,RMVar_hsa_circ_60159,RMVar_hsa_circ_205967 28411 RMVar_ID_28411 Human_SNP_ID_109379214 A-to-I Human chr2 + 202290136 202290136 202290136 CACCACCATGCCTGGCTAATTTTTGTATTTTTAATAGAGATGGGGTTTCACCATGTTGGCCAGGC CACCACCATGCCTGGCTAATTTTTGTATTTTTGATAGAGATGGGGTTTCACCATGTTGGCCAGGC A G NOP58 Ensembl:ENSG00000055044 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1373593516 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25500460 RMVar_hsa_circ_115742,RMVar_hsa_circ_205960,RMVar_hsa_circ_30972,RMVar_hsa_circ_51138,RMVar_hsa_circ_63084,RMVar_hsa_circ_331064,RMVar_hsa_circ_125140,RMVar_hsa_circ_334218,RMVar_hsa_circ_335529,RMVar_hsa_circ_69947,RMVar_hsa_circ_205965,RMVar_hsa_circ_355556,RMVar_hsa_circ_80453,RMVar_hsa_circ_358962,RMVar_hsa_circ_341238,RMVar_hsa_circ_60159,RMVar_hsa_circ_205967 28412 RMVar_ID_28412 Human_SNP_ID_109379647 A-to-I Human chr2 + 202291686 202291686 202291686 AAAATTAGCTGCGCGTGGTGGCGTACACCTGTAATCCCAGCTACTCGGGAGGCTGAGACAGGAGA AAAATTAGCTGCGCGTGGTGGCGTACACCTGTGATCCCAGCTACTCGGGAGGCTGAGACAGGAGA A G NOP58 Ensembl:ENSG00000055044 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1414787745 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115742,RMVar_hsa_circ_205960,RMVar_hsa_circ_30972,RMVar_hsa_circ_51138,RMVar_hsa_circ_63084,RMVar_hsa_circ_331064,RMVar_hsa_circ_125140,RMVar_hsa_circ_335529,RMVar_hsa_circ_69947,RMVar_hsa_circ_205965,RMVar_hsa_circ_358962,RMVar_hsa_circ_341238,RMVar_hsa_circ_99407,RMVar_hsa_circ_311734,RMVar_hsa_circ_317220,RMVar_hsa_circ_282013,RMVar_hsa_circ_299669,RMVar_hsa_circ_102304,RMVar_hsa_circ_205970,RMVar_hsa_circ_205972,RMVar_hsa_circ_205973,RMVar_hsa_circ_205971,RMVar_hsa_circ_205969,RMVar_hsa_circ_42710,RMVar_hsa_circ_55603 28413 RMVar_ID_28413 Human_SNP_ID_109380360 A-to-I Human chr2 + 202293746 202293746 202293746 GCATGTGCTGCCACCATGCCTGGCTAATTTTTATATTTTTAGTTGAGACAGGGTTTTTGCCATGT GCATGTGCTGCCACCATGCCTGGCTAATTTTTGTATTTTTAGTTGAGACAGGGTTTTTGCCATGT A G NOP58 Ensembl:ENSG00000055044 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs573141017 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13741588 RMVar_hsa_circ_115742,RMVar_hsa_circ_205960,RMVar_hsa_circ_51138,RMVar_hsa_circ_63084,RMVar_hsa_circ_331064,RMVar_hsa_circ_125140,RMVar_hsa_circ_69947,RMVar_hsa_circ_205965,RMVar_hsa_circ_358962,RMVar_hsa_circ_341238,RMVar_hsa_circ_99407,RMVar_hsa_circ_311734,RMVar_hsa_circ_282013,RMVar_hsa_circ_299669,RMVar_hsa_circ_102304,RMVar_hsa_circ_205970,RMVar_hsa_circ_205972,RMVar_hsa_circ_205973,RMVar_hsa_circ_205971,RMVar_hsa_circ_42710,RMVar_hsa_circ_55603,RMVar_hsa_circ_12947,RMVar_hsa_circ_296759,RMVar_hsa_circ_368523 28414 RMVar_ID_28414 Human_SNP_ID_109380656 A-to-I Human chr2 + 202294820 202294820 202294820 CCCCATCTCTACTAAAAATACAAAAAAAAATTAGCTGGGTGTAGTGGTGGGTGCCTGTAATCCCA CCCCATCTCTACTAAAAATACAAAAAAAAATTGGCTGGGTGTAGTGGTGGGTGCCTGTAATCCCA A G NOP58 Ensembl:ENSG00000055044 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs556671020 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115742,RMVar_hsa_circ_205960,RMVar_hsa_circ_51138,RMVar_hsa_circ_63084,RMVar_hsa_circ_331064,RMVar_hsa_circ_125140,RMVar_hsa_circ_69947,RMVar_hsa_circ_205965,RMVar_hsa_circ_358962,RMVar_hsa_circ_341238,RMVar_hsa_circ_99407,RMVar_hsa_circ_311734,RMVar_hsa_circ_282013,RMVar_hsa_circ_299669,RMVar_hsa_circ_102304,RMVar_hsa_circ_205970,RMVar_hsa_circ_205972,RMVar_hsa_circ_205973,RMVar_hsa_circ_205971,RMVar_hsa_circ_42710,RMVar_hsa_circ_55603,RMVar_hsa_circ_12947,RMVar_hsa_circ_296759,RMVar_hsa_circ_368523 28415 RMVar_ID_28415 Human_SNP_ID_109406648 A-to-I Human chr2 + 202393524 202393524 202393524 CGCCATGTTGCCCAGGCTGGTGTCAAACTCCTAGGCACAAGCGATCCTCCTGACTCAGCCTCCCA CGCCATGTTGCCCAGGCTGGTGTCAAACTCCTGGGCACAAGCGATCCTCCTGACTCAGCCTCCCA A G BMPR2 Ensembl:ENSG00000204217 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs961739403 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_205980,RMVar_hsa_circ_108219 28416 RMVar_ID_28416 Human_SNP_ID_109407649 A-to-I Human chr2 + 202397391 202397391 202397391 TAATATCTCCTTGAACCTTTAGAACTTGATCTATAGTCTCACTTAAGTAGATTACAGTAATAAGA TAATATCTCCTTGAACCTTTAGAACTTGATCTGTAGTCTCACTTAAGTAGATTACAGTAATAAGA A G BMPR2 Ensembl:ENSG00000204217 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1469982577 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_205980,RMVar_hsa_circ_108219 28417 RMVar_ID_28417 Human_SNP_ID_109410565 A-to-I Human chr2 + 202409218 202409218 202409218 AATACAAAAATTAATCAGGTGTGGTGGTGCACACCTGTAATCACAGCTATTTGGGTGGCTATGGC AATACAAAAATTAATCAGGTGTGGTGGTGCACGCCTGTAATCACAGCTATTTGGGTGGCTATGGC A G BMPR2 Ensembl:ENSG00000204217 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1258666275 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_205980,RMVar_hsa_circ_108219 28418 RMVar_ID_28418 Human_SNP_ID_109411704 A-to-I Human chr2 + 202413898 202413898 202413898 TGTTGCCTAGGCGGTGTGGAATTCCTGAGCTCAAGTGATCTGCCCACCTTAGCCTCCCAAAGTGC TGTTGCCTAGGCGGTGTGGAATTCCTGAGCTCGAGTGATCTGCCCACCTTAGCCTCCCAAAGTGC A G BMPR2 Ensembl:ENSG00000204217 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs933366237 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25500959 RMVar_hsa_circ_205980,RMVar_hsa_circ_108219 28419 RMVar_ID_28419 Human_SNP_ID_109414613 A-to-I Human chr2 + 202425128 202425128 202425128 CTACAGGCACATGCCACCATATTGGTCAGGCTAGTCTCGAACTCTTGACCTCAGGTGATCCACCT CTACAGGCACATGCCACCATATTGGTCAGGCTGGTCTCGAACTCTTGACCTCAGGTGATCCACCT A G BMPR2 Ensembl:ENSG00000204217 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs768055894 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_205980,RMVar_hsa_circ_108219 28420 RMVar_ID_28420 Human_SNP_ID_109415106 A-to-I Human chr2 + 202427253 202427253 202427253 GGTGATGTGTGCCTGGTACTTCCCAGCTACTCAGGAAGCTGAGGTGAGAGGATTGCTTAGGCCCG GGTGATGTGTGCCTGGTACTTCCCAGCTACTCGGGAAGCTGAGGTGAGAGGATTGCTTAGGCCCG A G BMPR2 Ensembl:ENSG00000204217 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs376362142 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_205980,RMVar_hsa_circ_108219 28421 RMVar_ID_28421 Human_SNP_ID_109415481 A-to-I Human chr2 + 202428616 202428616 202428616 TTTTGGTAGAGATGGGTCCTCGCTGTGTTGCCAGACTGGTCCTGAACTCCTGGGCTGAAGCGATC TTTTGGTAGAGATGGGTCCTCGCTGTGTTGCCGGACTGGTCCTGAACTCCTGGGCTGAAGCGATC A G BMPR2 Ensembl:ENSG00000204217 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1226085022 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13742569 RMVar_hsa_circ_205980,RMVar_hsa_circ_108219 28422 RMVar_ID_28422 Human_SNP_ID_109418099 A-to-I Human chr2 + 202439318 202439318 202439318 ACAATTGATTTTTATATATTGATGTATTCTGCAATGTTGTTGAACTTTTATTAGCTCTAGTAATT ACAATTGATTTTTATATATTGATGTATTCTGCGATGTTGTTGAACTTTTATTAGCTCTAGTAATT A G BMPR2 Ensembl:ENSG00000204217 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1287894583 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_205980,RMVar_hsa_circ_108219 28423 RMVar_ID_28423 Human_SNP_ID_109425510 A-to-I Human chr2 + 202467893 202467893 202467893 CAGCCTGGTGAAATCCCGTCTCTGCCAAAAGTAAAAAATTAGCCGGGCGTAGTGGTAGGCGCCTG CAGCCTGGTGAAATCCCGTCTCTGCCAAAAGTGAAAAATTAGCCGGGCGTAGTGGTAGGCGCCTG A G BMPR2 Ensembl:ENSG00000204217 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1232665270 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22599395 RMVar_hsa_circ_205990,RMVar_hsa_circ_321869,RMVar_hsa_circ_205980,RMVar_hsa_circ_108219,RMVar_hsa_circ_340116,RMVar_hsa_circ_365715,RMVar_hsa_circ_328616,RMVar_hsa_circ_103037,RMVar_hsa_circ_286067,RMVar_hsa_circ_305828,RMVar_hsa_circ_205984,RMVar_hsa_circ_205986,RMVar_hsa_circ_205988,RMVar_hsa_circ_205989,RMVar_hsa_circ_205987,RMVar_hsa_circ_205985,RMVar_hsa_circ_205994,RMVar_hsa_circ_313242,RMVar_hsa_circ_324449,RMVar_hsa_circ_371917,RMVar_hsa_circ_323643,RMVar_hsa_circ_303544,RMVar_hsa_circ_45353,RMVar_hsa_circ_112650,RMVar_hsa_circ_205996,RMVar_hsa_circ_205995,RMVar_hsa_circ_205992,RMVar_hsa_circ_205993,RMVar_hsa_circ_205991 28424 RMVar_ID_28424 Human_SNP_ID_109425511 A-to-I Human chr2 + 202467901 202467901 202467901 TGAAATCCCGTCTCTGCCAAAAGTAAAAAATTAGCCGGGCGTAGTGGTAGGCGCCTGTAATCCCG TGAAATCCCGTCTCTGCCAAAAGTAAAAAATTCGCCGGGCGTAGTGGTAGGCGCCTGTAATCCCG A C BMPR2 Ensembl:ENSG00000204217 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs71425943 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22599395,Human_RBP_ID_25501119 RMVar_hsa_circ_205990,RMVar_hsa_circ_321869,RMVar_hsa_circ_205980,RMVar_hsa_circ_108219,RMVar_hsa_circ_340116,RMVar_hsa_circ_365715,RMVar_hsa_circ_328616,RMVar_hsa_circ_103037,RMVar_hsa_circ_286067,RMVar_hsa_circ_305828,RMVar_hsa_circ_205984,RMVar_hsa_circ_205986,RMVar_hsa_circ_205988,RMVar_hsa_circ_205989,RMVar_hsa_circ_205987,RMVar_hsa_circ_205985,RMVar_hsa_circ_205994,RMVar_hsa_circ_313242,RMVar_hsa_circ_324449,RMVar_hsa_circ_371917,RMVar_hsa_circ_323643,RMVar_hsa_circ_303544,RMVar_hsa_circ_45353,RMVar_hsa_circ_112650,RMVar_hsa_circ_205996,RMVar_hsa_circ_205995,RMVar_hsa_circ_205992,RMVar_hsa_circ_205993,RMVar_hsa_circ_205991 28425 RMVar_ID_28425 Human_SNP_ID_109425512 A-to-I Human chr2 + 202467901 202467901 202467901 TGAAATCCCGTCTCTGCCAAAAGTAAAAAATTAGCCGGGCGTAGTGGTAGGCGCCTGTAATCCCG TGAAATCCCGTCTCTGCCAAAAGTAAAAAATTTGCCGGGCGTAGTGGTAGGCGCCTGTAATCCCG A T BMPR2 Ensembl:ENSG00000204217 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs71425943 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22599395,Human_RBP_ID_25501119 RMVar_hsa_circ_205990,RMVar_hsa_circ_321869,RMVar_hsa_circ_205980,RMVar_hsa_circ_108219,RMVar_hsa_circ_340116,RMVar_hsa_circ_365715,RMVar_hsa_circ_328616,RMVar_hsa_circ_103037,RMVar_hsa_circ_286067,RMVar_hsa_circ_305828,RMVar_hsa_circ_205984,RMVar_hsa_circ_205986,RMVar_hsa_circ_205988,RMVar_hsa_circ_205989,RMVar_hsa_circ_205987,RMVar_hsa_circ_205985,RMVar_hsa_circ_205994,RMVar_hsa_circ_313242,RMVar_hsa_circ_324449,RMVar_hsa_circ_371917,RMVar_hsa_circ_323643,RMVar_hsa_circ_303544,RMVar_hsa_circ_45353,RMVar_hsa_circ_112650,RMVar_hsa_circ_205996,RMVar_hsa_circ_205995,RMVar_hsa_circ_205992,RMVar_hsa_circ_205993,RMVar_hsa_circ_205991 28426 RMVar_ID_28426 Human_SNP_ID_109425526 A-to-I Human chr2 + 202467927 202467927 202467927 AAAATTAGCCGGGCGTAGTGGTAGGCGCCTGTAATCCCGCTACTCAGGAGGCTGAGACAGGAGAA AAAATTAGCCGGGCGTAGTGGTAGGCGCCTGTGATCCCGCTACTCAGGAGGCTGAGACAGGAGAA A G BMPR2 Ensembl:ENSG00000204217 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1024395724 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_205990,RMVar_hsa_circ_321869,RMVar_hsa_circ_205980,RMVar_hsa_circ_108219,RMVar_hsa_circ_340116,RMVar_hsa_circ_365715,RMVar_hsa_circ_328616,RMVar_hsa_circ_103037,RMVar_hsa_circ_286067,RMVar_hsa_circ_305828,RMVar_hsa_circ_205984,RMVar_hsa_circ_205986,RMVar_hsa_circ_205988,RMVar_hsa_circ_205989,RMVar_hsa_circ_205987,RMVar_hsa_circ_205985,RMVar_hsa_circ_205994,RMVar_hsa_circ_313242,RMVar_hsa_circ_324449,RMVar_hsa_circ_371917,RMVar_hsa_circ_323643,RMVar_hsa_circ_303544,RMVar_hsa_circ_45353,RMVar_hsa_circ_112650,RMVar_hsa_circ_205996,RMVar_hsa_circ_205995,RMVar_hsa_circ_205992,RMVar_hsa_circ_205993,RMVar_hsa_circ_205991 28427 RMVar_ID_28427 Human_SNP_ID_109425626 A-to-I Human chr2 + 202468403 202468403 202468403 GGGAGGCTGAGGTTGGAGATTTGCTTGAGCCTAGGAAGTTGAAGCTGCAGCTATTGTGCCACTGC GGGAGGCTGAGGTTGGAGATTTGCTTGAGCCTTGGAAGTTGAAGCTGCAGCTATTGTGCCACTGC A T BMPR2 Ensembl:ENSG00000204217 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs892411248 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_205990,RMVar_hsa_circ_321869,RMVar_hsa_circ_205980,RMVar_hsa_circ_108219,RMVar_hsa_circ_340116,RMVar_hsa_circ_365715,RMVar_hsa_circ_328616,RMVar_hsa_circ_103037,RMVar_hsa_circ_286067,RMVar_hsa_circ_305828,RMVar_hsa_circ_205984,RMVar_hsa_circ_205986,RMVar_hsa_circ_205988,RMVar_hsa_circ_205989,RMVar_hsa_circ_205987,RMVar_hsa_circ_205985,RMVar_hsa_circ_205994,RMVar_hsa_circ_313242,RMVar_hsa_circ_324449,RMVar_hsa_circ_371917,RMVar_hsa_circ_323643,RMVar_hsa_circ_303544,RMVar_hsa_circ_45353,RMVar_hsa_circ_112650,RMVar_hsa_circ_205996,RMVar_hsa_circ_205995,RMVar_hsa_circ_205992,RMVar_hsa_circ_205993,RMVar_hsa_circ_205991 28428 RMVar_ID_28428 Human_SNP_ID_109426071 A-to-I Human chr2 + 202470072 202470072 202470072 TAGGATTAAGAAAATAAGTTGAGGCTGGGTGCAGGGGCTCATACCTGTAATCCCAGCACTTTGGG TAGGATTAAGAAAATAAGTTGAGGCTGGGTGCGGGGGCTCATACCTGTAATCCCAGCACTTTGGG A G BMPR2 Ensembl:ENSG00000204217 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1448411373 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_205990,RMVar_hsa_circ_321869,RMVar_hsa_circ_205980,RMVar_hsa_circ_108219,RMVar_hsa_circ_340116,RMVar_hsa_circ_365715,RMVar_hsa_circ_328616,RMVar_hsa_circ_103037,RMVar_hsa_circ_286067,RMVar_hsa_circ_305828,RMVar_hsa_circ_205984,RMVar_hsa_circ_205986,RMVar_hsa_circ_205988,RMVar_hsa_circ_205989,RMVar_hsa_circ_205987,RMVar_hsa_circ_205985,RMVar_hsa_circ_205994,RMVar_hsa_circ_313242,RMVar_hsa_circ_324449,RMVar_hsa_circ_371917,RMVar_hsa_circ_323643,RMVar_hsa_circ_303544,RMVar_hsa_circ_45353,RMVar_hsa_circ_112650,RMVar_hsa_circ_205996,RMVar_hsa_circ_205995,RMVar_hsa_circ_205992,RMVar_hsa_circ_205993,RMVar_hsa_circ_205991 28429 RMVar_ID_28429 Human_SNP_ID_109426331 A-to-I Human chr2 + 202470974 202470974 202470974 CCAGCTACTTGAGAGGCTGAGGTGGGAGGATCACTTGAACTTGGGAAGTCAAGGCTGCATTGAGC CCAGCTACTTGAGAGGCTGAGGTGGGAGGATCCCTTGAACTTGGGAAGTCAAGGCTGCATTGAGC A C BMPR2 Ensembl:ENSG00000204217 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs752359977 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_205990,RMVar_hsa_circ_321869,RMVar_hsa_circ_205980,RMVar_hsa_circ_108219,RMVar_hsa_circ_340116,RMVar_hsa_circ_365715,RMVar_hsa_circ_328616,RMVar_hsa_circ_103037,RMVar_hsa_circ_286067,RMVar_hsa_circ_305828,RMVar_hsa_circ_205984,RMVar_hsa_circ_205986,RMVar_hsa_circ_205988,RMVar_hsa_circ_205989,RMVar_hsa_circ_205987,RMVar_hsa_circ_205985,RMVar_hsa_circ_205994,RMVar_hsa_circ_313242,RMVar_hsa_circ_324449,RMVar_hsa_circ_371917,RMVar_hsa_circ_323643,RMVar_hsa_circ_303544,RMVar_hsa_circ_45353,RMVar_hsa_circ_112650,RMVar_hsa_circ_205996,RMVar_hsa_circ_205995,RMVar_hsa_circ_205992,RMVar_hsa_circ_205993,RMVar_hsa_circ_205991 28430 RMVar_ID_28430 Human_SNP_ID_109443253 A-to-I Human chr2 + 202537001 202537001 202537001 CTCACTGCAGCACTGAACTCTTGGGCTCAAGCAGTCCTCCTGCTCAGCCTCCTGAGTAGCTAGGA CTCACTGCAGCACTGAACTCTTGGGCTCAAGCGGTCCTCCTGCTCAGCCTCCTGAGTAGCTAGGA A G BMPR2 Ensembl:ENSG00000204217 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017950864 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_205990,RMVar_hsa_circ_205980,RMVar_hsa_circ_108219,RMVar_hsa_circ_340116,RMVar_hsa_circ_365715,RMVar_hsa_circ_103037,RMVar_hsa_circ_205988,RMVar_hsa_circ_205989,RMVar_hsa_circ_205987,RMVar_hsa_circ_45353,RMVar_hsa_circ_112650,RMVar_hsa_circ_206000,RMVar_hsa_circ_334207,RMVar_hsa_circ_327919,RMVar_hsa_circ_114496,RMVar_hsa_circ_206001,RMVar_hsa_circ_121208,RMVar_hsa_circ_205999,RMVar_hsa_circ_268125,RMVar_hsa_circ_24642,RMVar_hsa_circ_75928,RMVar_hsa_circ_206011,RMVar_hsa_circ_206010,RMVar_hsa_circ_127174,RMVar_hsa_circ_265461,RMVar_hsa_circ_206013,RMVar_hsa_circ_323149,RMVar_hsa_circ_325441,RMVar_hsa_circ_87126,RMVar_hsa_circ_206016,RMVar_hsa_circ_206017,RMVar_hsa_circ_44916,RMVar_hsa_circ_206018,RMVar_hsa_circ_317506,RMVar_hsa_circ_339941,RMVar_hsa_circ_311985,RMVar_hsa_circ_92035,RMVar_hsa_circ_206019,RMVar_hsa_circ_206020 28431 RMVar_ID_28431 Human_SNP_ID_109443270 A-to-I Human chr2 + 202537062 202537062 202537062 AGGACTACAGGTGCATGCCACCACGCCCGGCTAGTATTTTATTTTTTGTCGAGACAGTGTTTTGC AGGACTACAGGTGCATGCCACCACGCCCGGCTGGTATTTTATTTTTTGTCGAGACAGTGTTTTGC A G BMPR2 Ensembl:ENSG00000204217 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs556951848 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_205990,RMVar_hsa_circ_205980,RMVar_hsa_circ_108219,RMVar_hsa_circ_340116,RMVar_hsa_circ_365715,RMVar_hsa_circ_103037,RMVar_hsa_circ_205988,RMVar_hsa_circ_205989,RMVar_hsa_circ_205987,RMVar_hsa_circ_45353,RMVar_hsa_circ_112650,RMVar_hsa_circ_206000,RMVar_hsa_circ_334207,RMVar_hsa_circ_327919,RMVar_hsa_circ_114496,RMVar_hsa_circ_206001,RMVar_hsa_circ_121208,RMVar_hsa_circ_205999,RMVar_hsa_circ_268125,RMVar_hsa_circ_24642,RMVar_hsa_circ_75928,RMVar_hsa_circ_206011,RMVar_hsa_circ_206010,RMVar_hsa_circ_127174,RMVar_hsa_circ_265461,RMVar_hsa_circ_206013,RMVar_hsa_circ_323149,RMVar_hsa_circ_325441,RMVar_hsa_circ_87126,RMVar_hsa_circ_206016,RMVar_hsa_circ_206017,RMVar_hsa_circ_44916,RMVar_hsa_circ_206018,RMVar_hsa_circ_317506,RMVar_hsa_circ_339941,RMVar_hsa_circ_311985,RMVar_hsa_circ_92035,RMVar_hsa_circ_206019,RMVar_hsa_circ_206020 28432 RMVar_ID_28432 Human_SNP_ID_109447059 A-to-I Human chr2 + 202552192 202552192 202552192 TTATATTTTTAGTAGAGATGGGGTTTCACCATATTGGCCAAACTGGTCTCAAACTCCTAACCTCA TTATATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAAACTGGTCTCAAACTCCTAACCTCA A G BMPR2 Ensembl:ENSG00000204217 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs111481730 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_205990,RMVar_hsa_circ_205980,RMVar_hsa_circ_108219,RMVar_hsa_circ_365715,RMVar_hsa_circ_103037,RMVar_hsa_circ_205988,RMVar_hsa_circ_205989,RMVar_hsa_circ_45353,RMVar_hsa_circ_112650,RMVar_hsa_circ_206000,RMVar_hsa_circ_334207,RMVar_hsa_circ_114496,RMVar_hsa_circ_121208,RMVar_hsa_circ_205999,RMVar_hsa_circ_268125,RMVar_hsa_circ_75928,RMVar_hsa_circ_206011,RMVar_hsa_circ_206010,RMVar_hsa_circ_127174,RMVar_hsa_circ_265461,RMVar_hsa_circ_206013,RMVar_hsa_circ_325441,RMVar_hsa_circ_87126,RMVar_hsa_circ_206017,RMVar_hsa_circ_206018,RMVar_hsa_circ_317506,RMVar_hsa_circ_311985,RMVar_hsa_circ_92035,RMVar_hsa_circ_206020,RMVar_hsa_circ_63767 28433 RMVar_ID_28433 Human_SNP_ID_109504591 A-to-I Human chr2 - 202785030 202785030 202785030 TATTTTTAGTAGAGACAGGGTTTCACTATGCTACCCAGGATGGTCTCGATCTCCTGACCTCATGA TATTTTTAGTAGAGACAGGGTTTCACTATGCTGCCCAGGATGGTCTCGATCTCCTGACCTCATGA T C ICA1L Ensembl:ENSG00000163596 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027939385 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_206036,RMVar_hsa_circ_265170,RMVar_hsa_circ_268555,RMVar_hsa_circ_206037,RMVar_hsa_circ_206035 28434 RMVar_ID_28434 Human_SNP_ID_109525340 A-to-I Human chr2 - 202874017 202874017 202874017 GGATTACAGGTGCACGCCACCACATGGGGCTAATTTTTGAATTTTTAGTAGAAACAGGGTTTCAC GGATTACAGGTGCACGCCACCACATGGGGCTACTTTTTGAATTTTTAGTAGAAACAGGGTTTCAC T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1013712406 Functional Loss SNV dbSNP153 33..33 33 - - - 28435 RMVar_ID_28435 Human_SNP_ID_109525959 A-to-I Human chr2 - 202876735 202876735 202876735 GAGACAGTCTTGCTGTGTTGCCCAGGCTGGTTATGAACTCTTGGCCTCAGGCAGTCCTCATGCCT GAGACAGTCTTGCTGTGTTGCCCAGGCTGGTTGTGAACTCTTGGCCTCAGGCAGTCCTCATGCCT T C WDR12 Ensembl:ENSG00000138442 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1241393607 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6874983,Human_RBP_ID_9964199,Human_RBP_ID_13743029 28436 RMVar_ID_28436 Human_SNP_ID_109525999 A-to-I Human chr2 - 202876925 202876925 202876925 CTAGTTTTTATTTTTGTTCATTTTTTAGAGACAGGGTCTCACTATGTTGCCCAAGCTAGAGTGCA CTAGTTTTTATTTTTGTTCATTTTTTAGAGACCGGGTCTCACTATGTTGCCCAAGCTAGAGTGCA T G WDR12 Ensembl:ENSG00000138442 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1317389887 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6874986 28437 RMVar_ID_28437 Human_SNP_ID_109526141 A-to-I Human chr2 - 202877418 202877418 202877418 GTCTTGAACTCCTGGGCTCAAGCTGTCTGCCCACCTGGACCTCCCAAAGTGCTGAGATTACAGGC GTCTTGAACTCCTGGGCTCAAGCTGTCTGCCCGCCTGGACCTCCCAAAGTGCTGAGATTACAGGC T C WDR12 Ensembl:ENSG00000138442 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs3177584 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13743051,Human_RBP_ID_25501517 28438 RMVar_ID_28438 Human_SNP_ID_109526148 A-to-I Human chr2 - 202877465 202877465 202877465 TATTACTTTTTTTGTAGAGAGAGGGTTTCGCCATGTAGCCCATGCTGGTCTTGAACTCCTGGGCT TATTACTTTTTTTGTAGAGAGAGGGTTTCGCCGTGTAGCCCATGCTGGTCTTGAACTCCTGGGCT T C WDR12 Ensembl:ENSG00000138442 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1452074142 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6874994,Human_RBP_ID_13743054 28439 RMVar_ID_28439 Human_SNP_ID_109526596 A-to-I Human chr2 - 202879483 202879483 202879483 CCAGGAGGTGGAGGTTGCAGTGAGCTGAGATCATACCACTGTGCTCCAGCCTGGGCAGCAGAGCC CCAGGAGGTGGAGGTTGCAGTGAGCTGAGATCGTACCACTGTGCTCCAGCCTGGGCAGCAGAGCC T C WDR12 Ensembl:ENSG00000138442 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1289262521 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2615472,Human_RBP_ID_4592942,Human_RBP_ID_10004496 28440 RMVar_ID_28440 Human_SNP_ID_109526652 A-to-I Human chr2 - 202879678 202879678 202879678 CTTGTAATCCCAGCATTTTGGGTGGCCAAGGCAGGCGGCTCACCTGAGGTCAGGGGTTCGAGACC CTTGTAATCCCAGCATTTTGGGTGGCCAAGGCGGGCGGCTCACCTGAGGTCAGGGGTTCGAGACC T C WDR12 Ensembl:ENSG00000138442 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs555936806 Functional Loss SNV dbSNP153 33..33 33 - - - 28441 RMVar_ID_28441 Human_SNP_ID_109526668 A-to-I Human chr2 - 202879759 202879759 202879759 CCAGCCTGGGTGACAGTGCAAGACTCTGTCTCAACAACAACGATAACAAAATATTGATTCGGCAG CCAGCCTGGGTGACAGTGCAAGACTCTGTCTCCACAACAACGATAACAAAATATTGATTCGGCAG T G WDR12 Ensembl:ENSG00000138442 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs985097122 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6875013 28442 RMVar_ID_28442 Human_SNP_ID_109526670 A-to-I Human chr2 - 202879777 202879777 202879777 AGATTGTGCCACTGCACTCCAGCCTGGGTGACAGTGCAAGACTCTGTCTCAACAACAACGATAAC AGATTGTGCCACTGCACTCCAGCCTGGGTGACTGTGCAAGACTCTGTCTCAACAACAACGATAAC T A WDR12 Ensembl:ENSG00000138442 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs750999633 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6875013 28443 RMVar_ID_28443 Human_SNP_ID_109526671 A-to-I Human chr2 - 202879777 202879777 202879777 AGATTGTGCCACTGCACTCCAGCCTGGGTGACAGTGCAAGACTCTGTCTCAACAACAACGATAAC AGATTGTGCCACTGCACTCCAGCCTGGGTGACGGTGCAAGACTCTGTCTCAACAACAACGATAAC T C WDR12 Ensembl:ENSG00000138442 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs750999633 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6875013 28444 RMVar_ID_28444 Human_SNP_ID_109526685 A-to-I Human chr2 - 202879858 202879858 202879858 GACCGCCTGTAATCCCAACTACTTGGGAGGCTAAGGCAGGAGAATTGCTTGAACCCGGGAGGCAG GACCGCCTGTAATCCCAACTACTTGGGAGGCTGAGGCAGGAGAATTGCTTGAACCCGGGAGGCAG T C WDR12 Ensembl:ENSG00000138442 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1559157142 Functional Loss SNV dbSNP153 33..33 33 - - - 28445 RMVar_ID_28445 Human_SNP_ID_109526792 A-to-I Human chr2 - 202880365 202880365 202880365 TTTTGTATTTTTAGTAGAGACGGGGTTTTGCCATGTTGGCCAGGCTGGTCTTGAACTCCTGACCT TTTTGTATTTTTAGTAGAGACGGGGTTTTGCCCTGTTGGCCAGGCTGGTCTTGAACTCCTGACCT T G WDR12 Ensembl:ENSG00000138442 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1393997385 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17570142 28446 RMVar_ID_28446 Human_SNP_ID_109528271 A-to-I Human chr2 - 202886024 202886024 202886024 CAGTGGCCCACTGCAGGAGTGGGCCTGGCTGGAGTGCAGTGGCGTGATGGTAGCTCACTGTAGCC CAGTGGCCCACTGCAGGAGTGGGCCTGGCTGGTGTGCAGTGGCGTGATGGTAGCTCACTGTAGCC T A WDR12 Ensembl:ENSG00000138442 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs898990200 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6875035,Human_RBP_ID_21894870 RMVar_hsa_circ_53102,RMVar_hsa_circ_206062,RMVar_hsa_circ_81516,RMVar_hsa_circ_74793,RMVar_hsa_circ_58248,RMVar_hsa_circ_31362,RMVar_hsa_circ_71001,RMVar_hsa_circ_334317,RMVar_hsa_circ_313561,RMVar_hsa_circ_206064,RMVar_hsa_circ_359019,RMVar_hsa_circ_285476,RMVar_hsa_circ_206065 28447 RMVar_ID_28447 Human_SNP_ID_109528272 A-to-I Human chr2 - 202886024 202886024 202886024 CAGTGGCCCACTGCAGGAGTGGGCCTGGCTGGAGTGCAGTGGCGTGATGGTAGCTCACTGTAGCC CAGTGGCCCACTGCAGGAGTGGGCCTGGCTGGGGTGCAGTGGCGTGATGGTAGCTCACTGTAGCC T C WDR12 Ensembl:ENSG00000138442 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs898990200 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6875035,Human_RBP_ID_21894870 RMVar_hsa_circ_53102,RMVar_hsa_circ_206062,RMVar_hsa_circ_81516,RMVar_hsa_circ_74793,RMVar_hsa_circ_58248,RMVar_hsa_circ_31362,RMVar_hsa_circ_71001,RMVar_hsa_circ_334317,RMVar_hsa_circ_313561,RMVar_hsa_circ_206064,RMVar_hsa_circ_359019,RMVar_hsa_circ_285476,RMVar_hsa_circ_206065 28448 RMVar_ID_28448 Human_SNP_ID_109561699 A-to-I Human chr2 + 203027853 203027853 203027853 CCTATTTCACCCTTCCAAGCAGCTAGGACTACAAGTGTGTGCCACCACACCTGGCTATTTTCTGA CCTATTTCACCCTTCCAAGCAGCTAGGACTACGAGTGTGTGCCACCACACCTGGCTATTTTCTGA A G NBEAL1 Ensembl:ENSG00000144426 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs936925144 Functional Loss SNV dbSNP153 33..33 33 - - - 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,RMVar_hsa_circ_206104,RMVar_hsa_circ_46687,RMVar_hsa_circ_111341,RMVar_hsa_circ_361618,RMVar_hsa_circ_206105 28449 RMVar_ID_28449 Human_SNP_ID_109562711 A-to-I Human chr2 + 203032396 203032396 203032396 GAAGATAAGAACAGCTGGGCACGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGC GAAGATAAGAACAGCTGGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGC A G NBEAL1 Ensembl:ENSG00000144426 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965571757 Functional Loss SNV dbSNP153 33..33 33 - - - 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,RMVar_hsa_circ_206104,RMVar_hsa_circ_46687,RMVar_hsa_circ_111341,RMVar_hsa_circ_361618,RMVar_hsa_circ_206105 28450 RMVar_ID_28450 Human_SNP_ID_109568619 A-to-I Human chr2 + 203058260 203058260 203058260 CACTATGTTGCCCAGACTGGTCTTGAATTCCTAGGCTCAAGTAATCCTCCCGCCTTAGCCTCCCA CACTATGTTGCCCAGACTGGTCTTGAATTCCTGGGCTCAAGTAATCCTCCCGCCTTAGCCTCCCA A G NBEAL1 Ensembl:ENSG00000144426 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900304074 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22987352 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,RMVar_hsa_circ_46687,RMVar_hsa_circ_111341,RMVar_hsa_circ_206105,RMVar_hsa_circ_333436,RMVar_hsa_circ_361593,RMVar_hsa_circ_310697,RMVar_hsa_circ_97033,RMVar_hsa_circ_11727,RMVar_hsa_circ_39698,RMVar_hsa_circ_54883,RMVar_hsa_circ_206108,RMVar_hsa_circ_206109,RMVar_hsa_circ_206107,RMVar_hsa_circ_206110,RMVar_hsa_circ_40958,RMVar_hsa_circ_104377,RMVar_hsa_circ_124661,RMVar_hsa_circ_286587,RMVar_hsa_circ_305718,RMVar_hsa_circ_319688,RMVar_hsa_circ_287236,RMVar_hsa_circ_120209,RMVar_hsa_circ_62522,RMVar_hsa_circ_206113,RMVar_hsa_circ_5335,RMVar_hsa_circ_9626,RMVar_hsa_circ_206115,RMVar_hsa_circ_206117,RMVar_hsa_circ_206118,RMVar_hsa_circ_206116,RMVar_hsa_circ_206114,RMVar_hsa_circ_115690,RMVar_hsa_circ_362776,RMVar_hsa_circ_352308,RMVar_hsa_circ_78980,RMVar_hsa_circ_206120,RMVar_hsa_circ_51416,RMVar_hsa_circ_206121,RMVar_hsa_circ_206119 28451 RMVar_ID_28451 Human_SNP_ID_109576958 A-to-I Human chr2 + 203095872 203095872 203095872 CCTGCTCACTGCAACCTCCACCTCCCGGGTTCAGGTGATTCTCCTGCCTCAGCCTCCCAAGTAGC CCTGCTCACTGCAACCTCCACCTCCCGGGTTCGGGTGATTCTCCTGCCTCAGCCTCCCAAGTAGC A G NBEAL1 Ensembl:ENSG00000144426 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs905107876 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104425,RMVar_hsa_circ_79681,RMVar_hsa_circ_83224,RMVar_hsa_circ_206102,RMVar_hsa_circ_206103,RMVar_hsa_circ_206101,RMVar_hsa_circ_111341,RMVar_hsa_circ_206105,RMVar_hsa_circ_97033,RMVar_hsa_circ_11727,RMVar_hsa_circ_39698,RMVar_hsa_circ_54883,RMVar_hsa_circ_206109,RMVar_hsa_circ_206110,RMVar_hsa_circ_104377,RMVar_hsa_circ_124661,RMVar_hsa_circ_305718,RMVar_hsa_circ_120209,RMVar_hsa_circ_62522,RMVar_hsa_circ_5335,RMVar_hsa_circ_9626,RMVar_hsa_circ_206117,RMVar_hsa_circ_206118,RMVar_hsa_circ_206116,RMVar_hsa_circ_115690,RMVar_hsa_circ_78980,RMVar_hsa_circ_6303,RMVar_hsa_circ_54727,RMVar_hsa_circ_316885,RMVar_hsa_circ_206120,RMVar_hsa_circ_51416,RMVar_hsa_circ_206121,RMVar_hsa_circ_206122,RMVar_hsa_circ_83477,RMVar_hsa_circ_10860,RMVar_hsa_circ_80575,RMVar_hsa_circ_206126,RMVar_hsa_circ_125717,RMVar_hsa_circ_206127,RMVar_hsa_circ_206128 28452 RMVar_ID_28452 Human_SNP_ID_109582066 A-to-I Human chr2 + 203117759 203117759 203117759 GTTGGAGTGTAGTGGTGGGATCATGGCCTACTATGGTCTTGAACTCCTGAGCTTAAGTAGTCCTC GTTGGAGTGTAGTGGTGGGATCATGGCCTACTGTGGTCTTGAACTCCTGAGCTTAAGTAGTCCTC A G NBEAL1 Ensembl:ENSG00000144426 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1373697006 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3397,RMVar_hsa_circ_104425,RMVar_hsa_circ_79681,RMVar_hsa_circ_83224,RMVar_hsa_circ_206102,RMVar_hsa_circ_206103,RMVar_hsa_circ_206101,RMVar_hsa_circ_11727,RMVar_hsa_circ_54883,RMVar_hsa_circ_206110,RMVar_hsa_circ_104377,RMVar_hsa_circ_124661,RMVar_hsa_circ_5335,RMVar_hsa_circ_9626,RMVar_hsa_circ_206118,RMVar_hsa_circ_115690,RMVar_hsa_circ_78980,RMVar_hsa_circ_54727,RMVar_hsa_circ_206120,RMVar_hsa_circ_51416,RMVar_hsa_circ_206121,RMVar_hsa_circ_47774,RMVar_hsa_circ_80575,RMVar_hsa_circ_206128,RMVar_hsa_circ_364407,RMVar_hsa_circ_21150,RMVar_hsa_circ_31562,RMVar_hsa_circ_10409,RMVar_hsa_circ_73313,RMVar_hsa_circ_294598,RMVar_hsa_circ_342918,RMVar_hsa_circ_354382,RMVar_hsa_circ_369656,RMVar_hsa_circ_378947,RMVar_hsa_circ_366441,RMVar_hsa_circ_351875,RMVar_hsa_circ_351934,RMVar_hsa_circ_343763,RMVar_hsa_circ_330115,RMVar_hsa_circ_332324,RMVar_hsa_circ_94708,RMVar_hsa_circ_84293,RMVar_hsa_circ_206133,RMVar_hsa_circ_206135,RMVar_hsa_circ_51465,RMVar_hsa_circ_206134,RMVar_hsa_circ_206131,RMVar_hsa_circ_206132,RMVar_hsa_circ_326021,RMVar_hsa_circ_206130,RMVar_hsa_circ_206138,RMVar_hsa_circ_206141,RMVar_hsa_circ_331071,RMVar_hsa_circ_343440,RMVar_hsa_circ_206142 28453 RMVar_ID_28453 Human_SNP_ID_109582068 A-to-I Human chr2 + 203117781 203117781 203117781 ATGGCCTACTATGGTCTTGAACTCCTGAGCTTAAGTAGTCCTCCCACCTTCAGTCTCCGGAGTAG ATGGCCTACTATGGTCTTGAACTCCTGAGCTTGAGTAGTCCTCCCACCTTCAGTCTCCGGAGTAG A G NBEAL1 Ensembl:ENSG00000144426 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs745494207 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3397,RMVar_hsa_circ_104425,RMVar_hsa_circ_79681,RMVar_hsa_circ_83224,RMVar_hsa_circ_206102,RMVar_hsa_circ_206103,RMVar_hsa_circ_206101,RMVar_hsa_circ_11727,RMVar_hsa_circ_54883,RMVar_hsa_circ_206110,RMVar_hsa_circ_104377,RMVar_hsa_circ_124661,RMVar_hsa_circ_5335,RMVar_hsa_circ_9626,RMVar_hsa_circ_206118,RMVar_hsa_circ_115690,RMVar_hsa_circ_78980,RMVar_hsa_circ_54727,RMVar_hsa_circ_206120,RMVar_hsa_circ_51416,RMVar_hsa_circ_206121,RMVar_hsa_circ_47774,RMVar_hsa_circ_80575,RMVar_hsa_circ_206128,RMVar_hsa_circ_364407,RMVar_hsa_circ_21150,RMVar_hsa_circ_31562,RMVar_hsa_circ_10409,RMVar_hsa_circ_73313,RMVar_hsa_circ_294598,RMVar_hsa_circ_342918,RMVar_hsa_circ_354382,RMVar_hsa_circ_369656,RMVar_hsa_circ_378947,RMVar_hsa_circ_366441,RMVar_hsa_circ_351875,RMVar_hsa_circ_351934,RMVar_hsa_circ_343763,RMVar_hsa_circ_330115,RMVar_hsa_circ_332324,RMVar_hsa_circ_94708,RMVar_hsa_circ_84293,RMVar_hsa_circ_206133,RMVar_hsa_circ_206135,RMVar_hsa_circ_51465,RMVar_hsa_circ_206134,RMVar_hsa_circ_206131,RMVar_hsa_circ_206132,RMVar_hsa_circ_326021,RMVar_hsa_circ_206130,RMVar_hsa_circ_206138,RMVar_hsa_circ_206141,RMVar_hsa_circ_331071,RMVar_hsa_circ_343440,RMVar_hsa_circ_206142 28454 RMVar_ID_28454 Human_SNP_ID_109582070 A-to-I Human chr2 + 203117785 203117785 203117785 CCTACTATGGTCTTGAACTCCTGAGCTTAAGTAGTCCTCCCACCTTCAGTCTCCGGAGTAGCTAG CCTACTATGGTCTTGAACTCCTGAGCTTAAGTGGTCCTCCCACCTTCAGTCTCCGGAGTAGCTAG A G NBEAL1 Ensembl:ENSG00000144426 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1449856534 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3397,RMVar_hsa_circ_104425,RMVar_hsa_circ_79681,RMVar_hsa_circ_83224,RMVar_hsa_circ_206102,RMVar_hsa_circ_206103,RMVar_hsa_circ_206101,RMVar_hsa_circ_11727,RMVar_hsa_circ_54883,RMVar_hsa_circ_206110,RMVar_hsa_circ_104377,RMVar_hsa_circ_124661,RMVar_hsa_circ_5335,RMVar_hsa_circ_9626,RMVar_hsa_circ_206118,RMVar_hsa_circ_115690,RMVar_hsa_circ_78980,RMVar_hsa_circ_54727,RMVar_hsa_circ_206120,RMVar_hsa_circ_51416,RMVar_hsa_circ_206121,RMVar_hsa_circ_47774,RMVar_hsa_circ_80575,RMVar_hsa_circ_206128,RMVar_hsa_circ_364407,RMVar_hsa_circ_21150,RMVar_hsa_circ_31562,RMVar_hsa_circ_10409,RMVar_hsa_circ_73313,RMVar_hsa_circ_294598,RMVar_hsa_circ_342918,RMVar_hsa_circ_354382,RMVar_hsa_circ_369656,RMVar_hsa_circ_378947,RMVar_hsa_circ_366441,RMVar_hsa_circ_351875,RMVar_hsa_circ_351934,RMVar_hsa_circ_343763,RMVar_hsa_circ_330115,RMVar_hsa_circ_332324,RMVar_hsa_circ_94708,RMVar_hsa_circ_84293,RMVar_hsa_circ_206133,RMVar_hsa_circ_206135,RMVar_hsa_circ_51465,RMVar_hsa_circ_206134,RMVar_hsa_circ_206131,RMVar_hsa_circ_206132,RMVar_hsa_circ_326021,RMVar_hsa_circ_206130,RMVar_hsa_circ_206138,RMVar_hsa_circ_206141,RMVar_hsa_circ_331071,RMVar_hsa_circ_343440,RMVar_hsa_circ_206142 28455 RMVar_ID_28455 Human_SNP_ID_109582072 A-to-I Human chr2 + 203117794 203117794 203117794 GTCTTGAACTCCTGAGCTTAAGTAGTCCTCCCACCTTCAGTCTCCGGAGTAGCTAGGACTACAGG GTCTTGAACTCCTGAGCTTAAGTAGTCCTCCCGCCTTCAGTCTCCGGAGTAGCTAGGACTACAGG A G NBEAL1 Ensembl:ENSG00000144426 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs888630383 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3397,RMVar_hsa_circ_104425,RMVar_hsa_circ_79681,RMVar_hsa_circ_83224,RMVar_hsa_circ_206102,RMVar_hsa_circ_206103,RMVar_hsa_circ_206101,RMVar_hsa_circ_11727,RMVar_hsa_circ_54883,RMVar_hsa_circ_206110,RMVar_hsa_circ_104377,RMVar_hsa_circ_124661,RMVar_hsa_circ_5335,RMVar_hsa_circ_9626,RMVar_hsa_circ_206118,RMVar_hsa_circ_115690,RMVar_hsa_circ_78980,RMVar_hsa_circ_54727,RMVar_hsa_circ_206120,RMVar_hsa_circ_51416,RMVar_hsa_circ_206121,RMVar_hsa_circ_47774,RMVar_hsa_circ_80575,RMVar_hsa_circ_206128,RMVar_hsa_circ_364407,RMVar_hsa_circ_21150,RMVar_hsa_circ_31562,RMVar_hsa_circ_10409,RMVar_hsa_circ_73313,RMVar_hsa_circ_294598,RMVar_hsa_circ_342918,RMVar_hsa_circ_354382,RMVar_hsa_circ_369656,RMVar_hsa_circ_378947,RMVar_hsa_circ_366441,RMVar_hsa_circ_351875,RMVar_hsa_circ_351934,RMVar_hsa_circ_343763,RMVar_hsa_circ_330115,RMVar_hsa_circ_332324,RMVar_hsa_circ_94708,RMVar_hsa_circ_84293,RMVar_hsa_circ_206133,RMVar_hsa_circ_206135,RMVar_hsa_circ_51465,RMVar_hsa_circ_206134,RMVar_hsa_circ_206131,RMVar_hsa_circ_206132,RMVar_hsa_circ_326021,RMVar_hsa_circ_206130,RMVar_hsa_circ_206138,RMVar_hsa_circ_206141,RMVar_hsa_circ_331071,RMVar_hsa_circ_343440,RMVar_hsa_circ_206142 28456 RMVar_ID_28456 Human_SNP_ID_109611801 A-to-I Human chr2 + 203240045 203240045 203240045 TTGAACCTGGGAGGCGGAGCTTGCAGTGAGCCAAGATCGCACCACTGCACTGCAGCCTGGCGACA TTGAACCTGGGAGGCGGAGCTTGCAGTGAGCCGAGATCGCACCACTGCACTGCAGCCTGGCGACA A G CYP20A1 Ensembl:ENSG00000119004 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978991172 Functional Loss SNV dbSNP153 33..33 33 - - - 28457 RMVar_ID_28457 Human_SNP_ID_109612345 A-to-I Human chr2 + 203242514 203242514 203242514 GAAACTGATGATGTAAGAAGCTTATGGCCAGCACGGTGACTCAAGCCTATAATCCCAGCACTTCG GAAACTGATGATGTAAGAAGCTTATGGCCAGCGCGGTGACTCAAGCCTATAATCCCAGCACTTCG A G CYP20A1 Ensembl:ENSG00000119004 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1436749482 Functional Loss SNV dbSNP153 33..33 33 - - - 28458 RMVar_ID_28458 Human_SNP_ID_109616863 A-to-I Human chr2 + 203259791 203259791 203259791 TGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGAAGAATCGCTTGAACCTGGCTAATTTTTGTATT TGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAACCTGGCTAATTTTTGTATT A G RN7SL670P,CYP20A1 Ensembl:ENSG00000264041,Ensembl:ENSG00000119004 Other,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs371559509 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_149,RMVar_hsa_circ_63848,RMVar_hsa_circ_329379,RMVar_hsa_circ_342953,RMVar_hsa_circ_339158,RMVar_hsa_circ_301536,RMVar_hsa_circ_67078,RMVar_hsa_circ_206195,RMVar_hsa_circ_364805,RMVar_hsa_circ_74386,RMVar_hsa_circ_16446,RMVar_hsa_circ_43642,RMVar_hsa_circ_343130,RMVar_hsa_circ_8771,RMVar_hsa_circ_206198,RMVar_hsa_circ_206200,RMVar_hsa_circ_206202,RMVar_hsa_circ_206203,RMVar_hsa_circ_206201,RMVar_hsa_circ_206199 28459 RMVar_ID_28459 Human_SNP_ID_109622174 A-to-I Human chr2 + 203281245 203281245 203281245 GAAGTATTAGGGGACCAGGCAAGGTGGCTCACAGCTATAATGCCAGCACTCTGGGAGGCCGAGGT GAAGTATTAGGGGACCAGGCAAGGTGGCTCACGGCTATAATGCCAGCACTCTGGGAGGCCGAGGT A G CYP20A1 Ensembl:ENSG00000119004 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs567863007 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_339158,RMVar_hsa_circ_364805,RMVar_hsa_circ_16446,RMVar_hsa_circ_43642,RMVar_hsa_circ_206198,RMVar_hsa_circ_206200,RMVar_hsa_circ_206199,RMVar_hsa_circ_334825,RMVar_hsa_circ_12258,RMVar_hsa_circ_206205,RMVar_hsa_circ_305981,RMVar_hsa_circ_363510,RMVar_hsa_circ_61493,RMVar_hsa_circ_206208,RMVar_hsa_circ_206209,RMVar_hsa_circ_206211,RMVar_hsa_circ_305767,RMVar_hsa_circ_334384,RMVar_hsa_circ_65386,RMVar_hsa_circ_330867 28460 RMVar_ID_28460 Human_SNP_ID_109622175 A-to-I Human chr2 + 203281249 203281249 203281249 TATTAGGGGACCAGGCAAGGTGGCTCACAGCTATAATGCCAGCACTCTGGGAGGCCGAGGTGGAT TATTAGGGGACCAGGCAAGGTGGCTCACAGCTGTAATGCCAGCACTCTGGGAGGCCGAGGTGGAT A G CYP20A1 Ensembl:ENSG00000119004 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs999713182 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_339158,RMVar_hsa_circ_364805,RMVar_hsa_circ_16446,RMVar_hsa_circ_43642,RMVar_hsa_circ_206198,RMVar_hsa_circ_206200,RMVar_hsa_circ_206199,RMVar_hsa_circ_334825,RMVar_hsa_circ_12258,RMVar_hsa_circ_206205,RMVar_hsa_circ_305981,RMVar_hsa_circ_363510,RMVar_hsa_circ_61493,RMVar_hsa_circ_206208,RMVar_hsa_circ_206209,RMVar_hsa_circ_206211,RMVar_hsa_circ_305767,RMVar_hsa_circ_334384,RMVar_hsa_circ_65386,RMVar_hsa_circ_330867 28461 RMVar_ID_28461 Human_SNP_ID_109623099 A-to-I Human chr2 + 203284960 203284960 203284960 TAGAGATGGGGTTTTGCCATGTTGCCCAGACTAGTCTTGAACTCCTGAGCCTACGCAATCCCCCA TAGAGATGGGGTTTTGCCATGTTGCCCAGACTGGTCTTGAACTCCTGAGCCTACGCAATCCCCCA A G CYP20A1 Ensembl:ENSG00000119004 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913431855 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_339158,RMVar_hsa_circ_364805,RMVar_hsa_circ_16446,RMVar_hsa_circ_43642,RMVar_hsa_circ_206198,RMVar_hsa_circ_206200,RMVar_hsa_circ_206199,RMVar_hsa_circ_334825,RMVar_hsa_circ_12258,RMVar_hsa_circ_206205,RMVar_hsa_circ_305981,RMVar_hsa_circ_363510,RMVar_hsa_circ_61493,RMVar_hsa_circ_206208,RMVar_hsa_circ_206209,RMVar_hsa_circ_206211,RMVar_hsa_circ_305767,RMVar_hsa_circ_334384,RMVar_hsa_circ_65386,RMVar_hsa_circ_330867 28462 RMVar_ID_28462 Human_SNP_ID_109625958 A-to-I Human chr2 + 203296061 203296061 203296061 GAGGCAGGAGGATCACTTGAGCCTAGGAGTTCAAGATCAGCCTGGGCAACCTAGGGAGAACCTGT GAGGCAGGAGGATCACTTGAGCCTAGGAGTTCGAGATCAGCCTGGGCAACCTAGGGAGAACCTGT A G CYP20A1 Ensembl:ENSG00000119004 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048458757 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_339158,RMVar_hsa_circ_61493,RMVar_hsa_circ_206213,RMVar_hsa_circ_331420,RMVar_hsa_circ_206214 28463 RMVar_ID_28463 Human_SNP_ID_109626304 A-to-I Human chr2 + 203297320 203297320 203297320 GCTGGGCGCGGTGGCTCACACCTGTAATCCCTACACTTTGGGAGGCTGAGGCAGGTGGATCACCT GCTGGGCGCGGTGGCTCACACCTGTAATCCCTGCACTTTGGGAGGCTGAGGCAGGTGGATCACCT A G CYP20A1 Ensembl:ENSG00000119004 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1044159568 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_206214 28464 RMVar_ID_28464 Human_SNP_ID_109626719 A-to-I Human chr2 + 203298718 203298718 203298718 TGAAACTCATTCTCAAAAAAAAAAAAAAAAGGAGGTGGGGAGAGCTATTTCAAGAATATTTTAAG TGAAACTCATTCTCAAAAAAAAAAAAAAAAGGGGGTGGGGAGAGCTATTTCAAGAATATTTTAAG A G CYP20A1 Ensembl:ENSG00000119004 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1012320869 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_206214 28465 RMVar_ID_28465 Human_SNP_ID_109626735 A-to-I Human chr2 + 203298785 203298785 203298785 GGCTGGGCACGGTAGCTCATGCCTGTTATCCTAACACTTTGGGAAGCCGACATGGGCAGATCACG GGCTGGGCACGGTAGCTCATGCCTGTTATCCTGACACTTTGGGAAGCCGACATGGGCAGATCACG A G CYP20A1 Ensembl:ENSG00000119004 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1049650552 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_206214 28466 RMVar_ID_28466 Human_SNP_ID_109626748 A-to-I Human chr2 + 203298847 203298847 203298847 ACGAGGTCAAGAGATTTGAGACCATCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATAC ACGAGGTCAAGAGATTTGAGACCATCCTGGCCGACATGGTGAAACCCCATCTCTACTAAAAATAC A G CYP20A1 Ensembl:ENSG00000119004 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1431418260 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_206214 28467 RMVar_ID_28467 Human_SNP_ID_109626782 A-to-I Human chr2 + 203298976 203298976 203298976 AGAATCGCTTGAACCTGGGAGGCGGAGGTTGCAGTGAGCTGATGTTGTGCTAGTGCACTCCAGCC AGAATCGCTTGAACCTGGGAGGCGGAGGTTGCGGTGAGCTGATGTTGTGCTAGTGCACTCCAGCC A G CYP20A1 Ensembl:ENSG00000119004 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs888622990 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_206214 28468 RMVar_ID_28468 Human_SNP_ID_109626866 A-to-I Human chr2 + 203299338 203299338 203299338 AATATACTCTGGTAGACTGAGGCGGGAGGATCACTTGAGCCCAGGAGTTGGAGGCTTCAGTGAGC AATATACTCTGGTAGACTGAGGCGGGAGGATCCCTTGAGCCCAGGAGTTGGAGGCTTCAGTGAGC A C CYP20A1 Ensembl:ENSG00000119004 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1470720879 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13744063 RMVar_hsa_circ_206214 28469 RMVar_ID_28469 Human_SNP_ID_109627443 A-to-I Human chr2 + 203301326 203301326 203301326 TTGACCAAGCTGGAGTGCATTGGCATGATCACAGCTTACTGTAGCCTCCACCTCCTGGGCTCCAG TTGACCAAGCTGGAGTGCATTGGCATGATCACGGCTTACTGTAGCCTCCACCTCCTGGGCTCCAG A G CYP20A1 Ensembl:ENSG00000119004 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1454112855 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6875509 28470 RMVar_ID_28470 Human_SNP_ID_109627628 A-to-I Human chr2 + 203302025 203302025 203302025 TCGGCTCACTGCAACCTCTGCTTCCCAGGTTCAAGTGATCCTCCCGCCTCAGCCTCCCAAGTAGC TCGGCTCACTGCAACCTCTGCTTCCCAGGTTCGAGTGATCCTCCCGCCTCAGCCTCCCAAGTAGC A G CYP20A1 Ensembl:ENSG00000119004 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs574264928 Functional Loss SNV dbSNP153 33..33 33 - - - 28471 RMVar_ID_28471 Human_SNP_ID_109627634 A-to-I Human chr2 + 203302043 203302043 203302043 TGCTTCCCAGGTTCAAGTGATCCTCCCGCCTCAGCCTCCCAAGTAGCTGGGATTGCAAACATGTG TGCTTCCCAGGTTCAAGTGATCCTCCCGCCTCGGCCTCCCAAGTAGCTGGGATTGCAAACATGTG A G CYP20A1 Ensembl:ENSG00000119004 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1014698778 Functional Loss SNV dbSNP153 33..33 33 - - - 28472 RMVar_ID_28472 Human_SNP_ID_109627656 A-to-I Human chr2 + 203302187 203302187 203302187 AACCTCAAGTAGTCTGCCCACCTTGACCTCCCAAAGTGCTGGGATTACAGGCATGGGGCACCATG AACCTCAAGTAGTCTGCCCACCTTGACCTCCCGAAGTGCTGGGATTACAGGCATGGGGCACCATG A G CYP20A1 Ensembl:ENSG00000119004 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1460474722 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17570148 28473 RMVar_ID_28473 Human_SNP_ID_109627657 A-to-I Human chr2 + 203302188 203302188 203302188 ACCTCAAGTAGTCTGCCCACCTTGACCTCCCAAAGTGCTGGGATTACAGGCATGGGGCACCATGC ACCTCAAGTAGTCTGCCCACCTTGACCTCCCAGAGTGCTGGGATTACAGGCATGGGGCACCATGC A G CYP20A1 Ensembl:ENSG00000119004 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1424647476 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17570148 28474 RMVar_ID_28474 Human_SNP_ID_109627680 A-to-I Human chr2 + 203302297 203302297 203302297 TCATGCCTATAACTCAAGCACTTTGGGAGTTCAAGGCGGCCAGATTGCTTGAGCTTTTAGAAGTT TCATGCCTATAACTCAAGCACTTTGGGAGTTCCAGGCGGCCAGATTGCTTGAGCTTTTAGAAGTT A C CYP20A1 Ensembl:ENSG00000119004 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1303828922 Functional Loss SNV dbSNP153 33..33 33 - - - 28475 RMVar_ID_28475 Human_SNP_ID_109627854 A-to-I Human chr2 + 203303002 203302998 203303002 CATGAGCCACCGCGCTCGGTCCCTTTCTTTTTATTTATTTATTTATTTTGAGATGGAGTCTCGCT CATGAGCCACCGCGCTCGGTCCCTTTCTT____TTTATTTATTTATTTTGAGATGGAGTCTCGCT TTTTA T CYP20A1 Ensembl:ENSG00000119004 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1045283312 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_6875520 28476 RMVar_ID_28476 Human_SNP_ID_109627862 A-to-I Human chr2 + 203303040 203303040 203303040 TTATTTATTTTGAGATGGAGTCTCGCTGTGTCACCCAGGCTGGAGTGTGGTGGCACGATCTTGGC TTATTTATTTTGAGATGGAGTCTCGCTGTGTCCCCCAGGCTGGAGTGTGGTGGCACGATCTTGGC A C CYP20A1 Ensembl:ENSG00000119004 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1277905720 Functional Loss SNV dbSNP153 33..33 33 - - - 28477 RMVar_ID_28477 Human_SNP_ID_109627899 A-to-I Human chr2 + 203303202 203303202 203303202 TTTGTATTTTTTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTAA TTTGTATTTTTTTTTAGTAGAGACAGGGTTTCGCCATGTTGGCCAGGCTGGTCTTGAACTCCTAA A G CYP20A1 Ensembl:ENSG00000119004 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1229050996 Functional Loss SNV dbSNP153 33..33 33 - - - 28478 RMVar_ID_28478 Human_SNP_ID_109628119 A-to-I Human chr2 + 203304018 203304018 203304018 AAAGTGGGCGTATAACTTGAGGTCAGGAGTTCAAGAACAGCCTGGCCAACATGGGGAAACCGCAT AAAGTGGGCGTATAACTTGAGGTCAGGAGTTCGAGAACAGCCTGGCCAACATGGGGAAACCGCAT A G CYP20A1 Ensembl:ENSG00000119004 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs190100188 Functional Loss SNV dbSNP153 33..33 33 - - - 28479 RMVar_ID_28479 Human_SNP_ID_109628223 A-to-I Human chr2 + 203304379 203304379 203304379 GCCTCCATGCCCAGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTAGCCAGGA GCCTCCATGCCCAGCTAATTTTTTGTATTTTTGGTAGAGACGGGGTTTCACCATGTTAGCCAGGA A G CYP20A1 Ensembl:ENSG00000119004 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1388187848 Functional Loss SNV dbSNP153 33..33 33 - - - 28480 RMVar_ID_28480 Human_SNP_ID_109628240 A-to-I Human chr2 + 203304457 203304457 203304457 CTGACCTTGTGATCTGTCCACCGCGGCTTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACAGCG CTGACCTTGTGATCTGTCCACCGCGGCTTCCCCAAGTGCTGGGATTACAGGTGTGAGCCACAGCG A C CYP20A1 Ensembl:ENSG00000119004 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs368306008 Functional Loss SNV dbSNP153 33..33 33 - - - 28481 RMVar_ID_28481 Human_SNP_ID_109628306 A-to-I Human chr2 + 203304771 203304771 203304771 TAGCCTAGGCAACATGGCGAAACTGCATCTCTACAAAAAATACAAAAATTAGCCAGGTGTGCTGG TAGCCTAGGCAACATGGCGAAACTGCATCTCTTCAAAAAATACAAAAATTAGCCAGGTGTGCTGG A T CYP20A1 Ensembl:ENSG00000119004 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs571298555 Functional Loss SNV dbSNP153 33..33 33 - - - 28482 RMVar_ID_28482 Human_SNP_ID_109628330 A-to-I Human chr2 + 203304881 203304881 203304881 TTGCTTGAGCCCAGGAGGTAGAGGTTGCAGTGAGCCATGATCATGCCACTGCACTCCAGCCTAGG TTGCTTGAGCCCAGGAGGTAGAGGTTGCAGTGGGCCATGATCATGCCACTGCACTCCAGCCTAGG A G CYP20A1 Ensembl:ENSG00000119004 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1465373592 Functional Loss SNV dbSNP153 33..33 33 - - - 28483 RMVar_ID_28483 Human_SNP_ID_109628331 A-to-I Human chr2 + 203304885 203304885 203304885 TTGAGCCCAGGAGGTAGAGGTTGCAGTGAGCCATGATCATGCCACTGCACTCCAGCCTAGGTGAC TTGAGCCCAGGAGGTAGAGGTTGCAGTGAGCCGTGATCATGCCACTGCACTCCAGCCTAGGTGAC A G CYP20A1 Ensembl:ENSG00000119004 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1406368037 Functional Loss SNV dbSNP153 33..33 33 - - - 28484 RMVar_ID_28484 Human_SNP_ID_109628441 A-to-I Human chr2 + 203305264 203305264 203305264 CCCTCTGTCACCAGGCTGGAGTGCAGTGGTGCAATCTCAGCTCACTGCAACCTCCCCCTCTCAGG CCCTCTGTCACCAGGCTGGAGTGCAGTGGTGCGATCTCAGCTCACTGCAACCTCCCCCTCTCAGG A G CYP20A1 Ensembl:ENSG00000119004 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1179347653 Functional Loss SNV dbSNP153 33..33 33 - - - 28485 RMVar_ID_28485 Human_SNP_ID_109628444 A-to-I Human chr2 + 203305275 203305275 203305275 CAGGCTGGAGTGCAGTGGTGCAATCTCAGCTCACTGCAACCTCCCCCTCTCAGGTTCAAGTAATT CAGGCTGGAGTGCAGTGGTGCAATCTCAGCTCGCTGCAACCTCCCCCTCTCAGGTTCAAGTAATT A G CYP20A1 Ensembl:ENSG00000119004 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs994430166 Functional Loss SNV dbSNP153 33..33 33 - - - 28486 RMVar_ID_28486 Human_SNP_ID_109628450 A-to-I Human chr2 + 203305304 203305304 203305304 CTCACTGCAACCTCCCCCTCTCAGGTTCAAGTAATTCTCCTGCCTCAGCCTGCCGAGTAGCTGGG CTCACTGCAACCTCCCCCTCTCAGGTTCAAGTGATTCTCCTGCCTCAGCCTGCCGAGTAGCTGGG A G CYP20A1 Ensembl:ENSG00000119004 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1264447563 Functional Loss SNV dbSNP153 33..33 33 - - - 28487 RMVar_ID_28487 Human_SNP_ID_109628493 A-to-I Human chr2 + 203305438 203305438 203305438 TTGCCAGGATGGTCTCGATCTCTTGTGCTCATAATCTACCTACCTCGGCCTCCCAAAGTGCTCGG TTGCCAGGATGGTCTCGATCTCTTGTGCTCATGATCTACCTACCTCGGCCTCCCAAAGTGCTCGG A G CYP20A1 Ensembl:ENSG00000119004 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1018569655 Functional Loss SNV dbSNP153 33..33 33 - - - 28488 RMVar_ID_28488 Human_SNP_ID_109628494 A-to-I Human chr2 + 203305443 203305443 203305443 AGGATGGTCTCGATCTCTTGTGCTCATAATCTACCTACCTCGGCCTCCCAAAGTGCTCGGATTAC AGGATGGTCTCGATCTCTTGTGCTCATAATCTGCCTACCTCGGCCTCCCAAAGTGCTCGGATTAC A G CYP20A1 Ensembl:ENSG00000119004 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs943790061 Functional Loss SNV dbSNP153 33..33 33 - - - 28489 RMVar_ID_28489 Human_SNP_ID_109628495 A-to-I Human chr2 + 203305443 203305443 203305443 AGGATGGTCTCGATCTCTTGTGCTCATAATCTACCTACCTCGGCCTCCCAAAGTGCTCGGATTAC AGGATGGTCTCGATCTCTTGTGCTCATAATCTTCCTACCTCGGCCTCCCAAAGTGCTCGGATTAC A T CYP20A1 Ensembl:ENSG00000119004 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs943790061 Functional Loss SNV dbSNP153 33..33 33 - - - 28490 RMVar_ID_28490 Human_SNP_ID_109628497 A-to-I Human chr2 + 203305447 203305447 203305447 TGGTCTCGATCTCTTGTGCTCATAATCTACCTACCTCGGCCTCCCAAAGTGCTCGGATTACAGAC TGGTCTCGATCTCTTGTGCTCATAATCTACCTCCCTCGGCCTCCCAAAGTGCTCGGATTACAGAC A C CYP20A1 Ensembl:ENSG00000119004 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1264385012 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2139,Human_miRNA_ID_5814,Human_miRNA_ID_9431,Human_miRNA_ID_12968,Human_miRNA_ID_16563,Human_miRNA_ID_20212,Human_miRNA_ID_23852,Human_miRNA_ID_27518 28491 RMVar_ID_28491 Human_SNP_ID_109628503 A-to-I Human chr2 + 203305460 203305459 203305460 TTGTGCTCATAATCTACCTACCTCGGCCTCCCAAAGTGCTCGGATTACAGACGTGAGCCACTGCG TTGTGCTCATAATCTACCTACCTCGGCCTCCC_AAGTGCTCGGATTACAGACGTGAGCCACTGCG CA C CYP20A1 Ensembl:ENSG00000119004 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1268474061 Functional Loss DEL dbSNP153 33..33 33 - - - 28492 RMVar_ID_28492 Human_SNP_ID_109638707 A-to-I Human chr2 + 203345618 203345618 203345618 TTTAGTAGAGATGGGGTTTCACCGTCTTGGCCAGTCTGGTCTCGAACTCCTGACTTCAGGTGATC TTTAGTAGAGATGGGGTTTCACCGTCTTGGCCGGTCTGGTCTCGAACTCCTGACTTCAGGTGATC A G ABI2 Ensembl:ENSG00000138443 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256498890 Functional Loss SNV dbSNP153 33..33 33 - - - 28493 RMVar_ID_28493 Human_SNP_ID_109674608 A-to-I Human chr2 - 203484447 203484447 203484447 TTTTTGGTTGTCCATCAAGGGCGTGTGCTACTACTGGCATCTAGTGGGTAGAGGCCAGAGGTGCT TTTTTGGTTGTCCATCAAGGGCGTGTGCTACTGCTGGCATCTAGTGGGTAGAGGCCAGAGGTGCT T C RAPH1 Ensembl:ENSG00000173166 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1014245807 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_359533,RMVar_hsa_circ_356930,RMVar_hsa_circ_206244,RMVar_hsa_circ_374986,RMVar_hsa_circ_45168,RMVar_hsa_circ_32085,RMVar_hsa_circ_206249,RMVar_hsa_circ_206251,RMVar_hsa_circ_104374,RMVar_hsa_circ_341667,RMVar_hsa_circ_343999,RMVar_hsa_circ_206252 28494 RMVar_ID_28494 Human_SNP_ID_109674937 A-to-I Human chr2 - 203485847 203485847 203485847 TTGGGCTAGATAGTTTTGTGAGTGGCTGTCCCATGCACTGTAGGATGTTTAGCAGCATCCCTGGC TTGGGCTAGATAGTTTTGTGAGTGGCTGTCCCGTGCACTGTAGGATGTTTAGCAGCATCCCTGGC T C RAPH1 Ensembl:ENSG00000173166 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1046345553 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13746456 RMVar_hsa_circ_359533,RMVar_hsa_circ_356930,RMVar_hsa_circ_206244,RMVar_hsa_circ_374986,RMVar_hsa_circ_45168,RMVar_hsa_circ_32085,RMVar_hsa_circ_206249,RMVar_hsa_circ_206251,RMVar_hsa_circ_104374,RMVar_hsa_circ_341667,RMVar_hsa_circ_343999,RMVar_hsa_circ_206252 28495 RMVar_ID_28495 Human_SNP_ID_110291287 A-to-I Human chr2 - 206007659 206007659 206007659 CACCACCATGCCCAGCTAATTTTTGTATTCTTAGTAGAGACAAGGTTTTGCCATGTTGACCAGGC CACCACCATGCCCAGCTAATTTTTGTATTCTTCGTAGAGACAAGGTTTTGCCATGTTGACCAGGC T G INO80D Ensembl:ENSG00000114933 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1422400463 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101389,RMVar_hsa_circ_117133,RMVar_hsa_circ_111361,RMVar_hsa_circ_206285,RMVar_hsa_circ_206287,RMVar_hsa_circ_87821,RMVar_hsa_circ_206288,RMVar_hsa_circ_206286,RMVar_hsa_circ_346157 28496 RMVar_ID_28496 Human_SNP_ID_110293899 A-to-I Human chr2 - 206018419 206018419 206018419 ACCATTGGCCAGGTGCAGTGGCTTATGCCTATAATCTCAACGCTTTGGGAGGCTGAGGCGGCTAG ACCATTGGCCAGGTGCAGTGGCTTATGCCTATCATCTCAACGCTTTGGGAGGCTGAGGCGGCTAG T G INO80D Ensembl:ENSG00000114933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1386403923 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79177,RMVar_hsa_circ_101389,RMVar_hsa_circ_117133,RMVar_hsa_circ_111361,RMVar_hsa_circ_206285,RMVar_hsa_circ_206287,RMVar_hsa_circ_87821,RMVar_hsa_circ_206288,RMVar_hsa_circ_206286,RMVar_hsa_circ_122216,RMVar_hsa_circ_206290,RMVar_hsa_circ_206291 28497 RMVar_ID_28497 Human_SNP_ID_110305793 A-to-I Human chr2 - 206068854 206068854 206068854 TCTACAAAAAATACAGAAAATTAGCACTGTGTAGTGGTATGTGCCTTTAGTCGCAGCTACTCAGG TCTACAAAAAATACAGAAAATTAGCACTGTGTGGTGGTATGTGCCTTTAGTCGCAGCTACTCAGG T C INO80D Ensembl:ENSG00000114933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs999121228 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79177,RMVar_hsa_circ_101389,RMVar_hsa_circ_206288,RMVar_hsa_circ_206291,RMVar_hsa_circ_206292 28498 RMVar_ID_28498 Human_SNP_ID_110305937 A-to-I Human chr2 - 206069495 206069495 206069495 GTGATCCACTCGCCTTGGCCTCCCAGAGTGCTAGGATTACAGGCATGAGCCACCACACTTGGCCA GTGATCCACTCGCCTTGGCCTCCCAGAGTGCTGGGATTACAGGCATGAGCCACCACACTTGGCCA T C INO80D Ensembl:ENSG00000114933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910720191 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79177,RMVar_hsa_circ_101389,RMVar_hsa_circ_206288,RMVar_hsa_circ_206291,RMVar_hsa_circ_206292 28499 RMVar_ID_28499 Human_SNP_ID_110306330 A-to-I Human chr2 - 206071096 206071096 206071096 AAATTACCTGAGCATGGTGGCATGCACCTGTAATCCCCGCTACTCAGGAGGCTGAGACAGGAGAA AAATTACCTGAGCATGGTGGCATGCACCTGTAGTCCCCGCTACTCAGGAGGCTGAGACAGGAGAA T C INO80D Ensembl:ENSG00000114933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs531970246 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79177,RMVar_hsa_circ_101389,RMVar_hsa_circ_206288,RMVar_hsa_circ_206291,RMVar_hsa_circ_206292 28500 RMVar_ID_28500 Human_SNP_ID_110307461 A-to-I Human chr2 - 206075869 206075869 206075869 ATTTGTATTTTGTAGAGACTGGGTTTCACCATATTGGCCGGGCTGGTCTCGAACTCCTGACCTCA ATTTGTATTTTGTAGAGACTGGGTTTCACCATTTTGGCCGGGCTGGTCTCGAACTCCTGACCTCA T A INO80D Ensembl:ENSG00000114933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1341479800 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79177,RMVar_hsa_circ_101389,RMVar_hsa_circ_206288,RMVar_hsa_circ_206291,RMVar_hsa_circ_206292 28501 RMVar_ID_28501 Human_SNP_ID_110307469 A-to-I Human chr2 - 206075901 206075901 206075901 ATTACAGGTGTGCACCACCAAGCCCAGCTAATATTTGTATTTTGTAGAGACTGGGTTTCACCATA ATTACAGGTGTGCACCACCAAGCCCAGCTAATTTTTGTATTTTGTAGAGACTGGGTTTCACCATA T A INO80D Ensembl:ENSG00000114933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs567883827 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79177,RMVar_hsa_circ_101389,RMVar_hsa_circ_206288,RMVar_hsa_circ_206291,RMVar_hsa_circ_206292 28502 RMVar_ID_28502 Human_SNP_ID_110307490 A-to-I Human chr2 - 206076005 206076005 206076005 CTCTATTGCCCAGGCTGGAGTGCAGTGGTGCTATCTTGGCTTACTGCAACCTCCACCTCCCGGGT CTCTATTGCCCAGGCTGGAGTGCAGTGGTGCTGTCTTGGCTTACTGCAACCTCCACCTCCCGGGT T C INO80D Ensembl:ENSG00000114933 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1164921423 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79177,RMVar_hsa_circ_101389,RMVar_hsa_circ_206288,RMVar_hsa_circ_206291,RMVar_hsa_circ_206292 28503 RMVar_ID_28503 Human_SNP_ID_110307544 A-to-I Human chr2 - 206076139 206076139 206076139 CCCAGCCTGGTGTTGAACTCCTGGGCTCAAGTAATCCTTCTGCCGTGGCCTCCCAACCTTCTGGT CCCAGCCTGGTGTTGAACTCCTGGGCTCAAGTGATCCTTCTGCCGTGGCCTCCCAACCTTCTGGT T C INO80D Ensembl:ENSG00000114933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1020352530 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13752278 RMVar_hsa_circ_79177,RMVar_hsa_circ_101389,RMVar_hsa_circ_206288,RMVar_hsa_circ_206291,RMVar_hsa_circ_206292 28504 RMVar_ID_28504 Human_SNP_ID_110308146 A-to-I Human chr2 - 206078561 206078561 206078561 AAACAAAGGGGCTCAAGTGATCCTTCTGCCTCAGCCTGCCATAGTGTTGGAATTACAGGTGTGAG AAACAAAGGGGCTCAAGTGATCCTTCTGCCTCCGCCTGCCATAGTGTTGGAATTACAGGTGTGAG T G INO80D Ensembl:ENSG00000114933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1331936670 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79177,RMVar_hsa_circ_101389,RMVar_hsa_circ_206288,RMVar_hsa_circ_206291,RMVar_hsa_circ_206292 28505 RMVar_ID_28505 Human_SNP_ID_110308304 A-to-I Human chr2 - 206079197 206079197 206079197 GTGGTAGTGCATTTTTGTAGTCCCAGCTACTCAGGAGGCTGAGGTGAGAGGATCGCTTGAACTCA GTGGTAGTGCATTTTTGTAGTCCCAGCTACTCGGGAGGCTGAGGTGAGAGGATCGCTTGAACTCA T C INO80D Ensembl:ENSG00000114933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1210628120 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17570152 RMVar_hsa_circ_79177,RMVar_hsa_circ_101389,RMVar_hsa_circ_206288,RMVar_hsa_circ_206291,RMVar_hsa_circ_206292 28506 RMVar_ID_28506 Human_SNP_ID_110317842 A-to-I Human chr2 - 206116703 206116703 206116703 TTTAAAAATATTTTATAGAGACAGGTCTCACTATGTTGCCCAGGCTCGTCTTGAACCCCTGGGCC TTTAAAAATATTTTATAGAGACAGGTCTCACTGTGTTGCCCAGGCTCGTCTTGAACCCCTGGGCC T C NDUFS1 Ensembl:ENSG00000023228 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1194839767 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4629734 28507 RMVar_ID_28507 Human_SNP_ID_110317847 A-to-I Human chr2 - 206116721 206116721 206116721 CACCGCGCCCAGCTAATTTTTAAAAATATTTTATAGAGACAGGTCTCACTATGTTGCCCAGGCTC CACCGCGCCCAGCTAATTTTTAAAAATATTTTGTAGAGACAGGTCTCACTATGTTGCCCAGGCTC T C NDUFS1 Ensembl:ENSG00000023228 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs963968143 Functional Loss SNV dbSNP153 33..33 33 - - - 28508 RMVar_ID_28508 Human_SNP_ID_110317862 A-to-I Human chr2 - 206116763 206116763 206116763 CCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTAAGCCACCGCGCCCAGCTAATTTTTAA CCCACCTCGGCCTCCCAAAGTGCTGGGATTACCGGCGTAAGCCACCGCGCCCAGCTAATTTTTAA T G NDUFS1 Ensembl:ENSG00000023228 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1170005439 Functional Loss SNV dbSNP153 33..33 33 - - - 28509 RMVar_ID_28509 Human_SNP_ID_110317863 A-to-I Human chr2 - 206116765 206116765 206116765 TGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTAAGCCACCGCGCCCAGCTAATTTTT TGCCCACCTCGGCCTCCCAAAGTGCTGGGATTTCAGGCGTAAGCCACCGCGCCCAGCTAATTTTT T A NDUFS1 Ensembl:ENSG00000023228 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1447149182 Functional Loss SNV dbSNP153 33..33 33 - - - 28510 RMVar_ID_28510 Human_SNP_ID_110317914 A-to-I Human chr2 - 206116967 206116967 206116967 TCGCCCAGGCTGAAGTGCAGTGGCACAATCTCAGCTCACTGCAACCTCCACCTCCCGGGTTCAGT TCGCCCAGGCTGAAGTGCAGTGGCACAATCTCGGCTCACTGCAACCTCCACCTCCCGGGTTCAGT T C NDUFS1 Ensembl:ENSG00000023228 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1413930918 Functional Loss SNV dbSNP153 33..33 33 - - - 28511 RMVar_ID_28511 Human_SNP_ID_110317915 A-to-I Human chr2 - 206116972 206116972 206116972 GTTTGTCGCCCAGGCTGAAGTGCAGTGGCACAATCTCAGCTCACTGCAACCTCCACCTCCCGGGT GTTTGTCGCCCAGGCTGAAGTGCAGTGGCACAGTCTCAGCTCACTGCAACCTCCACCTCCCGGGT T C NDUFS1 Ensembl:ENSG00000023228 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1032214592 Functional Loss SNV dbSNP153 33..33 33 - - - 28512 RMVar_ID_28512 Human_SNP_ID_110317921 A-to-I Human chr2 - 206116986 206116986 206116986 GAGACGGAGTCTCAGTTTGTCGCCCAGGCTGAAGTGCAGTGGCACAATCTCAGCTCACTGCAACC GAGACGGAGTCTCAGTTTGTCGCCCAGGCTGAGGTGCAGTGGCACAATCTCAGCTCACTGCAACC T C NDUFS1 Ensembl:ENSG00000023228 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs546623722 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17570153 28513 RMVar_ID_28513 Human_SNP_ID_110317941 A-to-I Human chr2 - 206117035 206117035 206117035 TGTGAGCCACCATGCCCCACTAATTTTTATTTATTTATTTTTTTTTTCTGAGACGGAGTCTCAGT TGTGAGCCACCATGCCCCACTAATTTTTATTTTTTTATTTTTTTTTTCTGAGACGGAGTCTCAGT T A NDUFS1 Ensembl:ENSG00000023228 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1265421455 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6878867 28514 RMVar_ID_28514 Human_SNP_ID_110317950 A-to-I Human chr2 - 206117094 206117094 206117094 AACCTCCCTGGATCAAGCAATCCTCCTGCCTCAGCCTCCTGAACAGCTGGAACTACAGGTGTGAG AACCTCCCTGGATCAAGCAATCCTCCTGCCTCGGCCTCCTGAACAGCTGGAACTACAGGTGTGAG T C NDUFS1 Ensembl:ENSG00000023228 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1309910627 Functional Loss SNV dbSNP153 33..33 33 - - - 28515 RMVar_ID_28515 Human_SNP_ID_110317972 A-to-I Human chr2 - 206117172 206117172 206117172 TTGATTGATTGACTGATTGAGGCAACTCTGTCACCCAGGCTGGGGTTCAGTGGCATGATCACAGT TTGATTGATTGACTGATTGAGGCAACTCTGTCCCCCAGGCTGGGGTTCAGTGGCATGATCACAGT T G NDUFS1 Ensembl:ENSG00000023228 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1257362656 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6878872,Human_RBP_ID_13752720 28516 RMVar_ID_28516 Human_SNP_ID_110318272 A-to-I Human chr2 - 206118369 206118369 206118369 CACCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGTACCCGGCCCCTAATA CACCTGCCTCAGCCTCCCAAAGTGCTGGGATTGCAGGCATGAGCCACTGTACCCGGCCCCTAATA T C NDUFS1 Ensembl:ENSG00000023228 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1028524466 Functional Loss SNV dbSNP153 33..33 33 - - - 28517 RMVar_ID_28517 Human_SNP_ID_110318314 A-to-I Human chr2 - 206118504 206118504 206118504 CTCCCACTTCAGTCTCCCAAGTGGCTGGGACTACAGGCACACGCCACCACACCTGGCTAATTTTT CTCCCACTTCAGTCTCCCAAGTGGCTGGGACTGCAGGCACACGCCACCACACCTGGCTAATTTTT T C NDUFS1 Ensembl:ENSG00000023228 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs576402711 Functional Loss SNV dbSNP153 33..33 33 - - - 28518 RMVar_ID_28518 Human_SNP_ID_110318457 A-to-I Human chr2 - 206119068 206119068 206119068 TCTTTGTTTTATCTTAGATTGAGTCTCACTGTATTGCCAGTCTGGAGTGCAGTGGCGCAATCTCA TCTTTGTTTTATCTTAGATTGAGTCTCACTGTGTTGCCAGTCTGGAGTGCAGTGGCGCAATCTCA T C NDUFS1 Ensembl:ENSG00000023228 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs570363135 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13752762,Human_RBP_ID_23182166,Human_RBP_ID_23850154 28519 RMVar_ID_28519 Human_SNP_ID_110318550 A-to-I Human chr2 - 206119439 206119439 206119439 CACCGTTGCACTCCAGCCTGGGTGACAGAGTGAGACTCTGTCTGAAAAAAAGTAAAAATTAAAAA CACCGTTGCACTCCAGCCTGGGTGACAGAGTGCGACTCTGTCTGAAAAAAAGTAAAAATTAAAAA T G NDUFS1 Ensembl:ENSG00000023228 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs772229851 Functional Loss SNV dbSNP153 33..33 33 - - - 28520 RMVar_ID_28520 Human_SNP_ID_110318622 A-to-I Human chr2 - 206119706 206119706 206119706 AATACATTAATTAAAAATATACTTGGCCTGGCACAGTAGCTCAAGCCTGTAATCCCAGCACTTTG AATACATTAATTAAAAATATACTTGGCCTGGCGCAGTAGCTCAAGCCTGTAATCCCAGCACTTTG T C NDUFS1 Ensembl:ENSG00000023228 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs989929336 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13752773,Human_RBP_ID_17948813 28521 RMVar_ID_28521 Human_SNP_ID_110319053 A-to-I Human chr2 - 206121511 206121511 206121511 AGTCAAGGCGGAGGTCGCGGTAAGCCGAGATCACACCATTGCACTGCAGCCTGGGTGAAGAAACA AGTCAAGGCGGAGGTCGCGGTAAGCCGAGATCGCACCATTGCACTGCAGCCTGGGTGAAGAAACA T C NDUFS1 Ensembl:ENSG00000023228 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1378328260 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26479240 28522 RMVar_ID_28522 Human_SNP_ID_110319073 A-to-I Human chr2 - 206121560 206121560 206121560 TAATCCCAGCTACTGGGGAGGCTGAAGCAGGAAAATCGCTTGAACTGAGAGTCAAGGCGGAGGTC TAATCCCAGCTACTGGGGAGGCTGAAGCAGGAGAATCGCTTGAACTGAGAGTCAAGGCGGAGGTC T C NDUFS1 Ensembl:ENSG00000023228 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1281539780 Functional Loss SNV dbSNP153 33..33 33 - - - 28523 RMVar_ID_28523 Human_SNP_ID_110319082 A-to-I Human chr2 - 206121609 206121609 206121609 GTCTCTACTAAAAATACAAAAATTAGCCAGGCATGGTGGCACATGGCTGTAATCCCAGCTACTGG GTCTCTACTAAAAATACAAAAATTAGCCAGGCCTGGTGGCACATGGCTGTAATCCCAGCTACTGG T G NDUFS1 Ensembl:ENSG00000023228 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1358248692 Functional Loss SNV dbSNP153 33..33 33 - - - 28524 RMVar_ID_28524 Human_SNP_ID_110319098 A-to-I Human chr2 - 206121680 206121680 206121680 TGGCAGGCTGAGGCGGGCAGATCATTGAGGTCAGGAGTTTGAGACCAGCCTGGCCAACGTGGTGA TGGCAGGCTGAGGCGGGCAGATCATTGAGGTCGGGAGTTTGAGACCAGCCTGGCCAACGTGGTGA T C NDUFS1 Ensembl:ENSG00000023228 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs374600835 Functional Loss SNV dbSNP153 33..33 33 - - - 28525 RMVar_ID_28525 Human_SNP_ID_110319110 A-to-I Human chr2 - 206121725 206121725 206121725 TGTCTGGACCGGGCGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGCAGGCTGAGGCGGGCAG TGTCTGGACCGGGCGCGGTGGCTCACACCTGTGATCCCAGCACTTTGGCAGGCTGAGGCGGGCAG T C NDUFS1 Ensembl:ENSG00000023228 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs545366328 Functional Loss SNV dbSNP153 33..33 33 - - - 28526 RMVar_ID_28526 Human_SNP_ID_110319112 A-to-I Human chr2 - 206121731 206121731 206121731 ATACCTTGTCTGGACCGGGCGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGCAGGCTGAGGC ATACCTTGTCTGGACCGGGCGCGGTGGCTCACCCCTGTAATCCCAGCACTTTGGCAGGCTGAGGC T G NDUFS1 Ensembl:ENSG00000023228 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1332106022 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13752815 28527 RMVar_ID_28527 Human_SNP_ID_110319222 A-to-I Human chr2 - 206122202 206122202 206122202 GGGGGTTCAAGGCAGGAAGATCAGTTGAGGCCAGGAGTTCAAGACCAGCCTGGACTGCATAGCAA GGGGGTTCAAGGCAGGAAGATCAGTTGAGGCCGGGAGTTCAAGACCAGCCTGGACTGCATAGCAA T C NDUFS1 Ensembl:ENSG00000023228 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1140904 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26479246 28528 RMVar_ID_28528 Human_SNP_ID_110319224 A-to-I Human chr2 - 206122207 206122207 206122207 ATTTTGGGGGTTCAAGGCAGGAAGATCAGTTGAGGCCAGGAGTTCAAGACCAGCCTGGACTGCAT ATTTTGGGGGTTCAAGGCAGGAAGATCAGTTGGGGCCAGGAGTTCAAGACCAGCCTGGACTGCAT T C NDUFS1 Ensembl:ENSG00000023228 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1140903 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26479246 28529 RMVar_ID_28529 Human_SNP_ID_110319226 A-to-I Human chr2 - 206122212 206122212 206122212 CCAGCATTTTGGGGGTTCAAGGCAGGAAGATCAGTTGAGGCCAGGAGTTCAAGACCAGCCTGGAC CCAGCATTTTGGGGGTTCAAGGCAGGAAGATCGGTTGAGGCCAGGAGTTCAAGACCAGCCTGGAC T C NDUFS1 Ensembl:ENSG00000023228 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1132859 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23182174,Human_RBP_ID_26479246 28530 RMVar_ID_28530 Human_SNP_ID_110319227 A-to-I Human chr2 - 206122212 206122212 206122212 CCAGCATTTTGGGGGTTCAAGGCAGGAAGATCAGTTGAGGCCAGGAGTTCAAGACCAGCCTGGAC CCAGCATTTTGGGGGTTCAAGGCAGGAAGATCCGTTGAGGCCAGGAGTTCAAGACCAGCCTGGAC T G NDUFS1 Ensembl:ENSG00000023228 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1132859 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23182174,Human_RBP_ID_26479246 28531 RMVar_ID_28531 Human_SNP_ID_110319230 A-to-I Human chr2 - 206122217 206122217 206122217 TAAGCCCAGCATTTTGGGGGTTCAAGGCAGGAAGATCAGTTGAGGCCAGGAGTTCAAGACCAGCC TAAGCCCAGCATTTTGGGGGTTCAAGGCAGGAGGATCAGTTGAGGCCAGGAGTTCAAGACCAGCC T C NDUFS1 Ensembl:ENSG00000023228 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1132858 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4593854,Human_RBP_ID_26479247 28532 RMVar_ID_28532 Human_SNP_ID_110319232 A-to-I Human chr2 - 206122221 206122221 206122221 CCTGTAAGCCCAGCATTTTGGGGGTTCAAGGCAGGAAGATCAGTTGAGGCCAGGAGTTCAAGACC CCTGTAAGCCCAGCATTTTGGGGGTTCAAGGCGGGAAGATCAGTTGAGGCCAGGAGTTCAAGACC T C NDUFS1 Ensembl:ENSG00000023228 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1132857 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26479247 28533 RMVar_ID_28533 Human_SNP_ID_110319233 A-to-I Human chr2 - 206122225 206122225 206122225 CACACCTGTAAGCCCAGCATTTTGGGGGTTCAAGGCAGGAAGATCAGTTGAGGCCAGGAGTTCAA CACACCTGTAAGCCCAGCATTTTGGGGGTTCAGGGCAGGAAGATCAGTTGAGGCCAGGAGTTCAA T C NDUFS1 Ensembl:ENSG00000023228 Protein coding 3'UTR GSE100210;GSE107867 HepG2 cell line;ASD brains,temporal_cortex - 29129909,30559470 RNA-Seq:(High) rs1440330107 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26479247 28534 RMVar_ID_28534 Human_SNP_ID_110319242 A-to-I Human chr2 - 206122247 206122247 206122247 AAAAACAGCAGGTGCAGTGGCTCACACCTGTAAGCCCAGCATTTTGGGGGTTCAAGGCAGGAAGA AAAAACAGCAGGTGCAGTGGCTCACACCTGTACGCCCAGCATTTTGGGGGTTCAAGGCAGGAAGA T G NDUFS1 Ensembl:ENSG00000023228 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs191367370 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26486802 28535 RMVar_ID_28535 Human_SNP_ID_110319243 A-to-I Human chr2 - 206122248 206122248 206122248 TAAAAACAGCAGGTGCAGTGGCTCACACCTGTAAGCCCAGCATTTTGGGGGTTCAAGGCAGGAAG TAAAAACAGCAGGTGCAGTGGCTCACACCTGTGAGCCCAGCATTTTGGGGGTTCAAGGCAGGAAG T C NDUFS1 Ensembl:ENSG00000023228 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1132856 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26486802 28536 RMVar_ID_28536 Human_SNP_ID_110319246 A-to-I Human chr2 - 206122264 206122264 206122264 TATGTTACAATATCTTTAAAAACAGCAGGTGCAGTGGCTCACACCTGTAAGCCCAGCATTTTGGG TATGTTACAATATCTTTAAAAACAGCAGGTGCGGTGGCTCACACCTGTAAGCCCAGCATTTTGGG T C NDUFS1 Ensembl:ENSG00000023228 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1053518 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6878903,Human_RBP_ID_17948821,Human_RBP_ID_26486802 28537 RMVar_ID_28537 Human_SNP_ID_110319276 A-to-I Human chr2 - 206122385 206122385 206122385 ACCTCAGGTGATCTACCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGC ACCTCAGGTGATCTACCTGCCTTGGCCTCCCACAGTGCTGGGATTACAGGCGTGAGCCACCGCGC T G NDUFS1 Ensembl:ENSG00000023228 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs186220792 Functional Loss SNV dbSNP153 33..33 33 - - - 28538 RMVar_ID_28538 Human_SNP_ID_110319300 A-to-I Human chr2 - 206122472 206122472 206122472 AGCGCACGCCACCACACCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCAATTTGG AGCGCACGCCACCACACCTGGCTAATTTTTGTGTTTTTAGTAGAGACAGGGTTTCACCAATTTGG T C NDUFS1 Ensembl:ENSG00000023228 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1421330883 Functional Loss SNV dbSNP153 33..33 33 - - - 28539 RMVar_ID_28539 Human_SNP_ID_110319302 A-to-I Human chr2 - 206122480 206122480 206122480 GGATTACAAGCGCACGCCACCACACCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCAC GGATTACAAGCGCACGCCACCACACCTGGCTAGTTTTTGTATTTTTAGTAGAGACAGGGTTTCAC T C NDUFS1 Ensembl:ENSG00000023228 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs910952639 Functional Loss SNV dbSNP153 33..33 33 - - - 28540 RMVar_ID_28540 Human_SNP_ID_110319304 A-to-I Human chr2 - 206122481 206122481 206122481 GGGATTACAAGCGCACGCCACCACACCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCA GGGATTACAAGCGCACGCCACCACACCTGGCTGATTTTTGTATTTTTAGTAGAGACAGGGTTTCA T C NDUFS1 Ensembl:ENSG00000023228 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1468513798 Functional Loss SNV dbSNP153 33..33 33 - - - 28541 RMVar_ID_28541 Human_SNP_ID_110319325 A-to-I Human chr2 - 206122546 206122546 206122546 TGGCTCACTGCAATCACCACCTCCCTGATTCAAGCGATTCTCCTGCCTCAGCCTCCCCGGTAGCT TGGCTCACTGCAATCACCACCTCCCTGATTCAGGCGATTCTCCTGCCTCAGCCTCCCCGGTAGCT T C NDUFS1 Ensembl:ENSG00000023228 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1022592921 Functional Loss SNV dbSNP153 33..33 33 - - - 28542 RMVar_ID_28542 Human_SNP_ID_110319462 A-to-I Human chr2 - 206122914 206122914 206122914 TCTGGGCAACATGGTGAAACCCCATCTCTACAAAAAATACAAAAATTAGCTGGGTGTGGTGGTGT TCTGGGCAACATGGTGAAACCCCATCTCTACAGAAAATACAAAAATTAGCTGGGTGTGGTGGTGT T C NDUFS1 Ensembl:ENSG00000023228 Protein coding 3'UTR GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1223060247 Functional Loss SNV dbSNP153 33..33 33 - - - 28543 RMVar_ID_28543 Human_SNP_ID_110322687 A-to-I Human chr2 - 206134822 206134822 206134822 CAGGCATACACCACCATGCCCAGCTAATTTTTATATTTTTTTGTATAGATGGGGCTCATTGTGAT CAGGCATACACCACCATGCCCAGCTAATTTTTGTATTTTTTTGTATAGATGGGGCTCATTGTGAT T C NDUFS1 Ensembl:ENSG00000023228 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs187922451 Functional Loss SNV dbSNP153 33..33 33 - - - 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_70745,RMVar_hsa_circ_325297,RMVar_hsa_circ_342117,RMVar_hsa_circ_378796,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_206316 28544 RMVar_ID_28544 Human_SNP_ID_110322692 A-to-I Human chr2 - 206134865 206134865 206134865 TTAAGCAGTCCTCCCACCTAAGCCTCCCCTGTAGCTGGGTCTGCAGGCATACACCACCATGCCCA TTAAGCAGTCCTCCCACCTAAGCCTCCCCTGTTGCTGGGTCTGCAGGCATACACCACCATGCCCA T A NDUFS1 Ensembl:ENSG00000023228 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs891674712 Functional Loss SNV dbSNP153 33..33 33 - - - 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_70745,RMVar_hsa_circ_325297,RMVar_hsa_circ_342117,RMVar_hsa_circ_378796,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_206316 28545 RMVar_ID_28545 Human_SNP_ID_110322707 A-to-I Human chr2 - 206134938 206134938 206134938 AGGTCTCACTATGTTGCCCAGGCTGCAGTGCAATGGCAGAATTGTAGCTGACTGTAGCCTCAAAC AGGTCTCACTATGTTGCCCAGGCTGCAGTGCAGTGGCAGAATTGTAGCTGACTGTAGCCTCAAAC T C NDUFS1 Ensembl:ENSG00000023228 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs12464101 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17570985 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_70745,RMVar_hsa_circ_325297,RMVar_hsa_circ_342117,RMVar_hsa_circ_378796,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_206316 28546 RMVar_ID_28546 Human_SNP_ID_110322878 A-to-I Human chr2 - 206135588 206135588 206135588 CGGCTCACTGCAACCTCAGTCTGCCAGGTTCAAGCGATTCTTGCCTCAGCCTCCCGAGTACCTGG CGGCTCACTGCAACCTCAGTCTGCCAGGTTCAGGCGATTCTTGCCTCAGCCTCCCGAGTACCTGG T C NDUFS1 Ensembl:ENSG00000023228 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1190335407 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13753011 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_70745,RMVar_hsa_circ_325297,RMVar_hsa_circ_342117,RMVar_hsa_circ_378796,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_206316 28547 RMVar_ID_28547 Human_SNP_ID_110323051 A-to-I Human chr2 - 206136188 206136188 206136188 ATACAAAAATTAGCCGGTTGTAGTGGCCTGTAATCCCAGCTACTTGAGAGGCTGGGGCAAGAGAA ATACAAAAATTAGCCGGTTGTAGTGGCCTGTAGTCCCAGCTACTTGAGAGGCTGGGGCAAGAGAA T C NDUFS1 Ensembl:ENSG00000023228 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs568937264 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13753017 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_70745,RMVar_hsa_circ_325297,RMVar_hsa_circ_342117,RMVar_hsa_circ_378796,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_206316 28548 RMVar_ID_28548 Human_SNP_ID_110328654 A-to-I Human chr2 - 206155555 206155555 206155555 AAATTTGCCGGGCATGTTGATGGGCGCCTGTAATCCCAACTACTCGGGAGGCTGAGAATTGCTTG AAATTTGCCGGGCATGTTGATGGGCGCCTGTAGTCCCAACTACTCGGGAGGCTGAGAATTGCTTG T C NDUFS1 Ensembl:ENSG00000023228 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs543958357 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267152,RMVar_hsa_circ_206339,RMVar_hsa_circ_109458 28549 RMVar_ID_28549 Human_SNP_ID_110328920 A-to-I Human chr2 - 206156431 206156431 206156431 AGCTGGGACCACAGGCGCATGCCACCACACCCAGCTAATTTTTTTTTTTTTTTGGTAGAGATGGG AGCTGGGACCACAGGCGCATGCCACCACACCCGGCTAATTTTTTTTTTTTTTTGGTAGAGATGGG T C NDUFS1 Ensembl:ENSG00000023228 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs369283755 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267152,RMVar_hsa_circ_206339,RMVar_hsa_circ_109458 28550 RMVar_ID_28550 Human_SNP_ID_110349226 A-to-I Human chr2 - 206236664 206236664 206236664 GAAAAGGAGCTGTTGAGAATAGCACAAATCCTAAAGGAACCCAAAGTGGCTGCTTCTATTTTGAA GAAAAGGAGCTGTTGAGAATAGCACAAATCCTGAAGGAACCCAAAGTGGCTGCTTCTATTTTGAA T C ATP5POP1 Ensembl:ENSG00000159186 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878862991 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1900899 28551 RMVar_ID_28551 Human_SNP_ID_110349227 A-to-I Human chr2 - 206236678 206236678 206236678 AGCTGGAGCAAGTAGAAAAGGAGCTGTTGAGAATAGCACAAATCCTAAAGGAACCCAAAGTGGCT AGCTGGAGCAAGTAGAAAAGGAGCTGTTGAGAGTAGCACAAATCCTAAAGGAACCCAAAGTGGCT T C ATP5POP1 Ensembl:ENSG00000159186 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879187571 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4594011 Human_miRNA_ID_1900899 28552 RMVar_ID_28552 Human_SNP_ID_110427240 A-to-I Human chr2 + 206553305 206553305 206553305 AAAAAATTAAAAAATTAGCCGGAGGTGGTGACATTTACCTGTAATCTCAGCTACTTGGGAGGCTG AAAAAATTAAAAAATTAGCCGGAGGTGGTGACGTTTACCTGTAATCTCAGCTACTTGGGAGGCTG A G ADAM23 Ensembl:ENSG00000114948 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1227734109 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25505185 RMVar_hsa_circ_3402,RMVar_hsa_circ_355924,RMVar_hsa_circ_361799,RMVar_hsa_circ_58284,RMVar_hsa_circ_71740,RMVar_hsa_circ_58963,RMVar_hsa_circ_282888,RMVar_hsa_circ_5866,RMVar_hsa_circ_41056,RMVar_hsa_circ_33384,RMVar_hsa_circ_123358,RMVar_hsa_circ_366199,RMVar_hsa_circ_73723,RMVar_hsa_circ_206360,RMVar_hsa_circ_206358,RMVar_hsa_circ_206359,RMVar_hsa_circ_80853 28553 RMVar_ID_28553 Human_SNP_ID_110434400 A-to-I Human chr2 + 206583435 206583435 206583435 GAGATAGTGCCACTGCACTCTGGCCTGGGCGAAAGAGCGAGACTCCGTCTCAAAAAAAAAAAAAA GAGATAGTGCCACTGCACTCTGGCCTGGGCGACAGAGCGAGACTCCGTCTCAAAAAAAAAAAAAA A C ADAM23 Ensembl:ENSG00000114948 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404572572 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58963,RMVar_hsa_circ_282888,RMVar_hsa_circ_9541,RMVar_hsa_circ_33384,RMVar_hsa_circ_73723,RMVar_hsa_circ_206360,RMVar_hsa_circ_80853,RMVar_hsa_circ_311463,RMVar_hsa_circ_294206,RMVar_hsa_circ_8644,RMVar_hsa_circ_206363,RMVar_hsa_circ_206364,RMVar_hsa_circ_378910,RMVar_hsa_circ_27097,RMVar_hsa_circ_24741,RMVar_hsa_circ_206367,RMVar_hsa_circ_206368,RMVar_hsa_circ_330575,RMVar_hsa_circ_41335,RMVar_hsa_circ_117924,RMVar_hsa_circ_206370,RMVar_hsa_circ_114311,RMVar_hsa_circ_206371,RMVar_hsa_circ_206372 28554 RMVar_ID_28554 Human_SNP_ID_110438875 A-to-I Human chr2 + 206601651 206601650 206601651 AAAAAATTAGCCAGTTGTGGTGGCATGTGCCCATAGTCCCAGCTACTTGGGAGGCTGAAGTGGGA AAAAAATTAGCCAGTTGTGGTGGCATGTGCCC_TAGTCCCAGCTACTTGGGAGGCTGAAGTGGGA CA C ADAM23 Ensembl:ENSG00000114948 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1238708610 Functional Loss DEL dbSNP153 33..33 33 - - - 28555 RMVar_ID_28555 Human_SNP_ID_110561387 A-to-I Human chr2 - 207105602 207105602 207105602 CTACCCTTCTTCAGGGCTTTCTGGCACAGCAAATAGGATGGACTGTGATGGAAGAAGGGTGGGGT CTACCCTTCTTCAGGGCTTTCTGGCACAGCAAGTAGGATGGACTGTGATGGAAGAAGGGTGGGGT T C KLF7 Ensembl:ENSG00000118263 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334948623 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_206387,RMVar_hsa_circ_302534,RMVar_hsa_circ_379046,RMVar_hsa_circ_206388 28556 RMVar_ID_28556 Human_SNP_ID_110561714 A-to-I Human chr2 - 207107010 207107010 207107010 CCTTACAAGGTAGGTGGTGATTTTCCCATCTTAGGCATGAGAACGTGGAAGCCTAGAAGATCCCA CCTTACAAGGTAGGTGGTGATTTTCCCATCTTTGGCATGAGAACGTGGAAGCCTAGAAGATCCCA T A KLF7 Ensembl:ENSG00000118263 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs866078478 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_206387,RMVar_hsa_circ_302534,RMVar_hsa_circ_379046,RMVar_hsa_circ_206388 28557 RMVar_ID_28557 Human_SNP_ID_110561715 A-to-I Human chr2 - 207107010 207107010 207107010 CCTTACAAGGTAGGTGGTGATTTTCCCATCTTAGGCATGAGAACGTGGAAGCCTAGAAGATCCCA CCTTACAAGGTAGGTGGTGATTTTCCCATCTTGGGCATGAGAACGTGGAAGCCTAGAAGATCCCA T C KLF7 Ensembl:ENSG00000118263 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs866078478 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_206387,RMVar_hsa_circ_302534,RMVar_hsa_circ_379046,RMVar_hsa_circ_206388 28558 RMVar_ID_28558 Human_SNP_ID_110637225 A-to-I Human chr2 - 207445902 207445902 207445902 TTTATAGAAACTCTAGAAAAACCCAGGGAAATATGCCTACTCCACAATTGTATATACTGTTTTAA TTTATAGAAACTCTAGAAAAACCCAGGGAAATTTGCCTACTCCACAATTGTATATACTGTTTTAA T A AC009226.1 Ensembl:ENSG00000223725 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs966701522 Functional Loss SNV dbSNP153 33..33 33 - - - 28559 RMVar_ID_28559 Human_SNP_ID_110651963 A-to-I Human chr2 - 207507576 207507576 207507576 CGTCCCCTGGGTTCAAGCGACTGTCATGTCTCAGCCTCTCGAGTAGCTGGGATTACAGGCACCCG CGTCCCCTGGGTTCAAGCGACTGTCATGTCTCGGCCTCTCGAGTAGCTGGGATTACAGGCACCCG T C AC009226.1 Ensembl:ENSG00000223725 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs758812589 Functional Loss SNV dbSNP153 33..33 33 - - - 28560 RMVar_ID_28560 Human_SNP_ID_110658722 A-to-I Human chr2 + 207535845 207535845 207535845 TATTTATTTTTATTTATTTATTTTTTTGAGGCAAGGTTTGGCTCTATCACCCAGGCTGGAGTGCA TATTTATTTTTATTTATTTATTTTTTTGAGGCGAGGTTTGGCTCTATCACCCAGGCTGGAGTGCA A G CREB1 Ensembl:ENSG00000118260 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1344403795 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13754785,Human_RBP_ID_22477881 RMVar_hsa_circ_206392,RMVar_hsa_circ_76849 28561 RMVar_ID_28561 Human_SNP_ID_110670918 A-to-I Human chr2 + 207584538 207584538 207584538 AGATTCTCGTGCCTCAGCCTCCCTGAGTAGTCAGGATTACAGGCACCTGCCACCACGTCTGATTT AGATTCTCGTGCCTCAGCCTCCCTGAGTAGTCGGGATTACAGGCACCTGCCACCACGTCTGATTT A G CREB1 Ensembl:ENSG00000118260 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1387069709 Functional Loss SNV dbSNP153 33..33 33 - - - 28562 RMVar_ID_28562 Human_SNP_ID_110675941 A-to-I Human chr2 - 207604861 207604858 207604862 AACATGTTACAATGGATCAACCTCAACAACACATTAAAGCTAGACGAAAGAAGTAATACACAGTG AACATGTTACAATGGATCAACCTCAACAACA____AAAGCTAGACGAAAGAAGTAATACACAGTG TAATG T METTL21A Ensembl:ENSG00000144401 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1328261530 Functional Loss DEL dbSNP153 32..35 33 - - - 28563 RMVar_ID_28563 Human_SNP_ID_110675942 A-to-I Human chr2 - 207604861 207604861 207604861 AACATGTTACAATGGATCAACCTCAACAACACATTAAAGCTAGACGAAAGAAGTAATACACAGTG AACATGTTACAATGGATCAACCTCAACAACACGTTAAAGCTAGACGAAAGAAGTAATACACAGTG T C METTL21A Ensembl:ENSG00000144401 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2551930 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_2862,GWAS_ID_2863,GWAS_ID_2864,GWAS_ID_2865,GWAS_ID_2866,GWAS_ID_2867,GWAS_ID_2868,GWAS_ID_2869,GWAS_ID_2870,GWAS_ID_2871,GWAS_ID_2872,GWAS_ID_2873,GWAS_ID_2874,GWAS_ID_2875,GWAS_ID_2876,GWAS_ID_2877,GWAS_ID_2878,GWAS_ID_2879,GWAS_ID_2880,GWAS_ID_2881,GWAS_ID_2882,GWAS_ID_2883,GWAS_ID_2884,GWAS_ID_2885,GWAS_ID_2886,GWAS_ID_2887,GWAS_ID_2888,GWAS_ID_2889,GWAS_ID_2890,GWAS_ID_2891,GWAS_ID_2892,GWAS_ID_2893,GWAS_ID_2894,GWAS_ID_2895,GWAS_ID_2896,GWAS_ID_2897,GWAS_ID_2898,GWAS_ID_2899,GWAS_ID_2900,GWAS_ID_2901,GWAS_ID_2902,GWAS_ID_2903,GWAS_ID_2904,GWAS_ID_2905,GWAS_ID_2906,GWAS_ID_2907,GWAS_ID_2908,GWAS_ID_2909,GWAS_ID_2910,GWAS_ID_2911,GWAS_ID_2912,GWAS_ID_2913,GWAS_ID_2914,GWAS_ID_2915,GWAS_ID_2916,GWAS_ID_2917,GWAS_ID_2918,GWAS_ID_2919,GWAS_ID_2920,GWAS_ID_2921,GWAS_ID_2922,GWAS_ID_2923,GWAS_ID_2924,GWAS_ID_2925,GWAS_ID_2926,GWAS_ID_2927,GWAS_ID_2928,GWAS_ID_2929,GWAS_ID_2930,GWAS_ID_2931,GWAS_ID_2932,GWAS_ID_2933,GWAS_ID_2934,GWAS_ID_2935,GWAS_ID_2936,GWAS_ID_2937,GWAS_ID_2938,GWAS_ID_2939,GWAS_ID_2940,GWAS_ID_2941,GWAS_ID_2942,GWAS_ID_2943,GWAS_ID_2944,GWAS_ID_2945,GWAS_ID_2946,GWAS_ID_2947,GWAS_ID_2948,GWAS_ID_2949,GWAS_ID_2950,GWAS_ID_2951,GWAS_ID_2952,GWAS_ID_2953,GWAS_ID_2954,GWAS_ID_2955,GWAS_ID_2956,GWAS_ID_2957,GWAS_ID_2958,GWAS_ID_2959,GWAS_ID_2960,GWAS_ID_2961,GWAS_ID_2962,GWAS_ID_2963,GWAS_ID_2964,GWAS_ID_2965,GWAS_ID_2966,GWAS_ID_2967,GWAS_ID_2968,GWAS_ID_2969,GWAS_ID_2970,GWAS_ID_2971,GWAS_ID_2972,GWAS_ID_2973,GWAS_ID_2974,GWAS_ID_2975,GWAS_ID_2976,GWAS_ID_2977,GWAS_ID_2978,GWAS_ID_2979,GWAS_ID_2980,GWAS_ID_2981,GWAS_ID_2982,GWAS_ID_2983,GWAS_ID_2984,GWAS_ID_2985,GWAS_ID_2986,GWAS_ID_2987,GWAS_ID_2988,GWAS_ID_2989,GWAS_ID_2990,GWAS_ID_2991,GWAS_ID_2992,GWAS_ID_2993,GWAS_ID_2994,GWAS_ID_2995,GWAS_ID_2996,GWAS_ID_2997,GWAS_ID_2998,GWAS_ID_2999,GWAS_ID_3000,GWAS_ID_3001,GWAS_ID_3002,GWAS_ID_3003,GWAS_ID_3004,GWAS_ID_3005,GWAS_ID_3006,GWAS_ID_3007,GWAS_ID_3008,GWAS_ID_3009,GWAS_ID_3010,GWAS_ID_3011,GWAS_ID_3012,GWAS_ID_3013,GWAS_ID_3014,GWAS_ID_3015,GWAS_ID_3016,GWAS_ID_3017,GWAS_ID_3018,GWAS_ID_3019,GWAS_ID_3020,GWAS_ID_3021,GWAS_ID_3022,GWAS_ID_3023,GWAS_ID_3024,GWAS_ID_3025,GWAS_ID_3026,GWAS_ID_3027,GWAS_ID_3028,GWAS_ID_3029,GWAS_ID_3030,GWAS_ID_3031,GWAS_ID_3032,GWAS_ID_3033,GWAS_ID_3034,GWAS_ID_3035,GWAS_ID_3036,GWAS_ID_3037,GWAS_ID_3038,GWAS_ID_3039,GWAS_ID_3040,GWAS_ID_3041,GWAS_ID_3042 28564 RMVar_ID_28564 Human_SNP_ID_110676492 A-to-I Human chr2 - 207607202 207607202 207607202 TGTATTTTTAGTAGAGATGGGGTTTTAATTATATTGGCCAGGCTGGTCTTGAACTCTTGACCTCG TGTATTTTTAGTAGAGATGGGGTTTTAATTATGTTGGCCAGGCTGGTCTTGAACTCTTGACCTCG T C METTL21A Ensembl:ENSG00000144401 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1235706575 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6880189 28565 RMVar_ID_28565 Human_SNP_ID_110676867 A-to-I Human chr2 - 207608864 207608864 207608864 TGGAGTGCGGGGCACGATCTCAGCTCACTGCAAGCTCCGCCTCCCGTATTCACGCCATTCTCCTG TGGAGTGCGGGGCACGATCTCAGCTCACTGCAGGCTCCGCCTCCCGTATTCACGCCATTCTCCTG T C METTL21A Ensembl:ENSG00000144401 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1482075110 Functional Loss SNV dbSNP153 33..33 33 - - - 28566 RMVar_ID_28566 Human_SNP_ID_110677477 A-to-I Human chr2 - 207612238 207612238 207612238 AAAATTAGCCGGGCGTGGTGTCAGGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA AAAATTAGCCGGGCGTGGTGTCAGGCGCCTGTTATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA T A METTL21A Ensembl:ENSG00000144401 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1373450258 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103976,RMVar_hsa_circ_206408 28567 RMVar_ID_28567 Human_SNP_ID_110677536 A-to-I Human chr2 - 207612456 207612456 207612456 TGCCTTAATTTCAGGTATATATATATATATAAATAAAGGAATTAAGTAAAAATAAAATTTCAGTT TGCCTTAATTTCAGGTATATATATATATATAATTAAAGGAATTAAGTAAAAATAAAATTTCAGTT T A METTL21A Ensembl:ENSG00000144401 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs2252982 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_3043,GWAS_ID_3044,GWAS_ID_3045,GWAS_ID_3046,GWAS_ID_3047,GWAS_ID_3048,GWAS_ID_3049,GWAS_ID_3050,GWAS_ID_3051,GWAS_ID_3052,GWAS_ID_3053,GWAS_ID_3054,GWAS_ID_3055,GWAS_ID_3056,GWAS_ID_3057,GWAS_ID_3058,GWAS_ID_3059,GWAS_ID_3060,GWAS_ID_3061,GWAS_ID_3062,GWAS_ID_3063,GWAS_ID_3064,GWAS_ID_3065,GWAS_ID_3066,GWAS_ID_3067,GWAS_ID_3068,GWAS_ID_3069,GWAS_ID_3070,GWAS_ID_3071,GWAS_ID_3072,GWAS_ID_3073,GWAS_ID_3074,GWAS_ID_3075,GWAS_ID_3076,GWAS_ID_3077,GWAS_ID_3078,GWAS_ID_3079,GWAS_ID_3080,GWAS_ID_3081,GWAS_ID_3082,GWAS_ID_3083,GWAS_ID_3084,GWAS_ID_3085,GWAS_ID_3086,GWAS_ID_3087,GWAS_ID_3088,GWAS_ID_3089,GWAS_ID_3090,GWAS_ID_3091,GWAS_ID_3092,GWAS_ID_3093,GWAS_ID_3094,GWAS_ID_3095,GWAS_ID_3096,GWAS_ID_3097,GWAS_ID_3098,GWAS_ID_3099,GWAS_ID_3100,GWAS_ID_3101,GWAS_ID_3102,GWAS_ID_3103,GWAS_ID_3104,GWAS_ID_3105,GWAS_ID_3106,GWAS_ID_3107,GWAS_ID_3108,GWAS_ID_3109,GWAS_ID_3110,GWAS_ID_3111,GWAS_ID_3112,GWAS_ID_3113,GWAS_ID_3114,GWAS_ID_3115,GWAS_ID_3116,GWAS_ID_3117,GWAS_ID_3118,GWAS_ID_3119,GWAS_ID_3120,GWAS_ID_3121,GWAS_ID_3122,GWAS_ID_3123,GWAS_ID_3124,GWAS_ID_3125,GWAS_ID_3126,GWAS_ID_3127,GWAS_ID_3128,GWAS_ID_3129,GWAS_ID_3130,GWAS_ID_3131,GWAS_ID_3132,GWAS_ID_3133,GWAS_ID_3134,GWAS_ID_3135,GWAS_ID_3136,GWAS_ID_3137,GWAS_ID_3138,GWAS_ID_3139,GWAS_ID_3140,GWAS_ID_3141,GWAS_ID_3142,GWAS_ID_3143,GWAS_ID_3144,GWAS_ID_3145,GWAS_ID_3146,GWAS_ID_3147,GWAS_ID_3148,GWAS_ID_3149,GWAS_ID_3150,GWAS_ID_3151,GWAS_ID_3152,GWAS_ID_3153,GWAS_ID_3154,GWAS_ID_3155,GWAS_ID_3156,GWAS_ID_3157,GWAS_ID_3158,GWAS_ID_3159,GWAS_ID_3160,GWAS_ID_3161,GWAS_ID_3162,GWAS_ID_3163,GWAS_ID_3164,GWAS_ID_3165,GWAS_ID_3166,GWAS_ID_3167,GWAS_ID_3168,GWAS_ID_3169,GWAS_ID_3170,GWAS_ID_3171,GWAS_ID_3172,GWAS_ID_3173,GWAS_ID_3174,GWAS_ID_3175,GWAS_ID_3176,GWAS_ID_3177,GWAS_ID_3178,GWAS_ID_3179,GWAS_ID_3180,GWAS_ID_3181,GWAS_ID_3182,GWAS_ID_3183,GWAS_ID_3184,GWAS_ID_3185,GWAS_ID_3186,GWAS_ID_3187,GWAS_ID_3188,GWAS_ID_3189,GWAS_ID_3190,GWAS_ID_3191,GWAS_ID_3192,GWAS_ID_3193,GWAS_ID_3194,GWAS_ID_3195,GWAS_ID_3196,GWAS_ID_3197,GWAS_ID_3198,GWAS_ID_3199,GWAS_ID_3200,GWAS_ID_3201,GWAS_ID_3202,GWAS_ID_3203,GWAS_ID_3204,GWAS_ID_3205,GWAS_ID_3206,GWAS_ID_3207,GWAS_ID_3208,GWAS_ID_3209,GWAS_ID_3210,GWAS_ID_3211,GWAS_ID_3212,GWAS_ID_3213,GWAS_ID_3214,GWAS_ID_3215,GWAS_ID_3216,GWAS_ID_3217,GWAS_ID_3218,GWAS_ID_3219,GWAS_ID_3220,GWAS_ID_3221,GWAS_ID_3222,GWAS_ID_3223 RMVar_hsa_circ_103976,RMVar_hsa_circ_206408 28568 RMVar_ID_28568 Human_SNP_ID_110677537 A-to-I Human chr2 - 207612456 207612456 207612456 TGCCTTAATTTCAGGTATATATATATATATAAATAAAGGAATTAAGTAAAAATAAAATTTCAGTT TGCCTTAATTTCAGGTATATATATATATATAAGTAAAGGAATTAAGTAAAAATAAAATTTCAGTT T C METTL21A Ensembl:ENSG00000144401 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs2252982 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_3043,GWAS_ID_3044,GWAS_ID_3045,GWAS_ID_3046,GWAS_ID_3047,GWAS_ID_3048,GWAS_ID_3049,GWAS_ID_3050,GWAS_ID_3051,GWAS_ID_3052,GWAS_ID_3053,GWAS_ID_3054,GWAS_ID_3055,GWAS_ID_3056,GWAS_ID_3057,GWAS_ID_3058,GWAS_ID_3059,GWAS_ID_3060,GWAS_ID_3061,GWAS_ID_3062,GWAS_ID_3063,GWAS_ID_3064,GWAS_ID_3065,GWAS_ID_3066,GWAS_ID_3067,GWAS_ID_3068,GWAS_ID_3069,GWAS_ID_3070,GWAS_ID_3071,GWAS_ID_3072,GWAS_ID_3073,GWAS_ID_3074,GWAS_ID_3075,GWAS_ID_3076,GWAS_ID_3077,GWAS_ID_3078,GWAS_ID_3079,GWAS_ID_3080,GWAS_ID_3081,GWAS_ID_3082,GWAS_ID_3083,GWAS_ID_3084,GWAS_ID_3085,GWAS_ID_3086,GWAS_ID_3087,GWAS_ID_3088,GWAS_ID_3089,GWAS_ID_3090,GWAS_ID_3091,GWAS_ID_3092,GWAS_ID_3093,GWAS_ID_3094,GWAS_ID_3095,GWAS_ID_3096,GWAS_ID_3097,GWAS_ID_3098,GWAS_ID_3099,GWAS_ID_3100,GWAS_ID_3101,GWAS_ID_3102,GWAS_ID_3103,GWAS_ID_3104,GWAS_ID_3105,GWAS_ID_3106,GWAS_ID_3107,GWAS_ID_3108,GWAS_ID_3109,GWAS_ID_3110,GWAS_ID_3111,GWAS_ID_3112,GWAS_ID_3113,GWAS_ID_3114,GWAS_ID_3115,GWAS_ID_3116,GWAS_ID_3117,GWAS_ID_3118,GWAS_ID_3119,GWAS_ID_3120,GWAS_ID_3121,GWAS_ID_3122,GWAS_ID_3123,GWAS_ID_3124,GWAS_ID_3125,GWAS_ID_3126,GWAS_ID_3127,GWAS_ID_3128,GWAS_ID_3129,GWAS_ID_3130,GWAS_ID_3131,GWAS_ID_3132,GWAS_ID_3133,GWAS_ID_3134,GWAS_ID_3135,GWAS_ID_3136,GWAS_ID_3137,GWAS_ID_3138,GWAS_ID_3139,GWAS_ID_3140,GWAS_ID_3141,GWAS_ID_3142,GWAS_ID_3143,GWAS_ID_3144,GWAS_ID_3145,GWAS_ID_3146,GWAS_ID_3147,GWAS_ID_3148,GWAS_ID_3149,GWAS_ID_3150,GWAS_ID_3151,GWAS_ID_3152,GWAS_ID_3153,GWAS_ID_3154,GWAS_ID_3155,GWAS_ID_3156,GWAS_ID_3157,GWAS_ID_3158,GWAS_ID_3159,GWAS_ID_3160,GWAS_ID_3161,GWAS_ID_3162,GWAS_ID_3163,GWAS_ID_3164,GWAS_ID_3165,GWAS_ID_3166,GWAS_ID_3167,GWAS_ID_3168,GWAS_ID_3169,GWAS_ID_3170,GWAS_ID_3171,GWAS_ID_3172,GWAS_ID_3173,GWAS_ID_3174,GWAS_ID_3175,GWAS_ID_3176,GWAS_ID_3177,GWAS_ID_3178,GWAS_ID_3179,GWAS_ID_3180,GWAS_ID_3181,GWAS_ID_3182,GWAS_ID_3183,GWAS_ID_3184,GWAS_ID_3185,GWAS_ID_3186,GWAS_ID_3187,GWAS_ID_3188,GWAS_ID_3189,GWAS_ID_3190,GWAS_ID_3191,GWAS_ID_3192,GWAS_ID_3193,GWAS_ID_3194,GWAS_ID_3195,GWAS_ID_3196,GWAS_ID_3197,GWAS_ID_3198,GWAS_ID_3199,GWAS_ID_3200,GWAS_ID_3201,GWAS_ID_3202,GWAS_ID_3203,GWAS_ID_3204,GWAS_ID_3205,GWAS_ID_3206,GWAS_ID_3207,GWAS_ID_3208,GWAS_ID_3209,GWAS_ID_3210,GWAS_ID_3211,GWAS_ID_3212,GWAS_ID_3213,GWAS_ID_3214,GWAS_ID_3215,GWAS_ID_3216,GWAS_ID_3217,GWAS_ID_3218,GWAS_ID_3219,GWAS_ID_3220,GWAS_ID_3221,GWAS_ID_3222,GWAS_ID_3223 RMVar_hsa_circ_103976,RMVar_hsa_circ_206408 28569 RMVar_ID_28569 Human_SNP_ID_110678031 A-to-I Human chr2 - 207614524 207614524 207614524 TAAGTTGGCTGCTTCATAACAGCCTAAGGAGAAGTGGACTGGGATTTCTTAGTAGCCAATTTATT TAAGTTGGCTGCTTCATAACAGCCTAAGGAGAGGTGGACTGGGATTTCTTAGTAGCCAATTTATT T C METTL21A Ensembl:ENSG00000144401 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900631978 Functional Loss SNV dbSNP153 33..33 33 - - - 28570 RMVar_ID_28570 Human_SNP_ID_110678034 A-to-I Human chr2 - 207614538 207614538 207614538 ATACGTAAAACATGTAAGTTGGCTGCTTCATAACAGCCTAAGGAGAAGTGGACTGGGATTTCTTA ATACGTAAAACATGTAAGTTGGCTGCTTCATATCAGCCTAAGGAGAAGTGGACTGGGATTTCTTA T A METTL21A Ensembl:ENSG00000144401 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1397857324 Functional Loss SNV dbSNP153 33..33 33 - - - 28571 RMVar_ID_28571 Human_SNP_ID_110714874 A-to-I Human chr2 + 207754767 207754767 207754767 TCAAGCCATCCTCTAGCCTCAGCCACACAAGTAGCTGGGACTACAAGTGCAACTGGCACCTGTCT TCAAGCCATCCTCTAGCCTCAGCCACACAAGTGGCTGGGACTACAAGTGCAACTGGCACCTGTCT A G CCNYL1 Ensembl:ENSG00000163249 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE107867 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;ASD brains,temporal_cortex - 23474544,24183664,29129909,30559470 RNA-Seq:(High) rs1413986919 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_206420,RMVar_hsa_circ_99464 28572 RMVar_ID_28572 Human_SNP_ID_110714885 A-to-I Human chr2 + 207754807 207754807 207754807 CTACAAGTGCAACTGGCACCTGTCTCCTGAATATTAAGCTTTTAATTTTTTGTTTCGGTCACTCT CTACAAGTGCAACTGGCACCTGTCTCCTGAATGTTAAGCTTTTAATTTTTTGTTTCGGTCACTCT A G MIR4775,CCNYL1 Ensembl:ENSG00000284079,Ensembl:ENSG00000163249 miRNA,Protein coding exon,3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1187453694 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2764834 RMVar_hsa_circ_206420,RMVar_hsa_circ_99464 28573 RMVar_ID_28573 Human_SNP_ID_110714902 A-to-I Human chr2 - 207754881 207754881 207754881 CCACACCCAGCTTCATTTTGCAAATTTTGAATATAAAGCTTTTAATTTTTTGTTTCAGTCAATGT CCACACCCAGCTTCATTTTGCAAATTTTGAATGTAAAGCTTTTAATTTTTTGTTTCAGTCAATGT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs779269630 Functional Loss SNV dbSNP153 33..33 33 - - - 28574 RMVar_ID_28574 Human_SNP_ID_110714936 A-to-I Human chr2 + 207755025 207755025 207755025 GTACCATGATGGTGCCTATAGGAATAGCTACTACACTCCAACCTGGACAACGTTATCAAGACCCC GTACCATGATGGTGCCTATAGGAATAGCTACTGCACTCCAACCTGGACAACGTTATCAAGACCCC A G CCNYL1 Ensembl:ENSG00000163249 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line - 23474544,24183664,29129909,29796672,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs1180841782 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_206420,RMVar_hsa_circ_99464 28575 RMVar_ID_28575 Human_SNP_ID_110715004 A-to-I Human chr2 + 207755259 207755259 207755259 AAAAATAGTTGGATATGGTGGCATGTGTCTGTAGTCCCAGCCACTCTGGAGGCTAAGGTGGGAGG AAAAATAGTTGGATATGGTGGCATGTGTCTGTGGTCCCAGCCACTCTGGAGGCTAAGGTGGGAGG A G CCNYL1 Ensembl:ENSG00000163249 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1354991586 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4594513,Human_RBP_ID_26487582 RMVar_hsa_circ_206420,RMVar_hsa_circ_99464 28576 RMVar_ID_28576 Human_SNP_ID_110715028 A-to-I Human chr2 + 207755350 207755350 207755350 TGCAGTGGGCCATGATCATGTCACTGCTCTCCAACCTGGGCGACATCCAGACCCTGTCTCAAAGA TGCAGTGGGCCATGATCATGTCACTGCTCTCCGACCTGGGCGACATCCAGACCCTGTCTCAAAGA A G CCNYL1 Ensembl:ENSG00000163249 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs937801574 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_206420,RMVar_hsa_circ_99464 28577 RMVar_ID_28577 Human_SNP_ID_110715045 A-to-I Human chr2 + 207755419 207755419 207755419 AGCAGAAGAAAAATGTTCAGACAAGGTTTTGTAAAGGTTTGTAGCATTTATATTTCTACAAGTAT AGCAGAAGAAAAATGTTCAGACAAGGTTTTGTGAAGGTTTGTAGCATTTATATTTCTACAAGTAT A G CCNYL1 Ensembl:ENSG00000163249 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1043068 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6880313,Human_RBP_ID_18314148,Human_RBP_ID_27691939 RMVar_hsa_circ_206420,RMVar_hsa_circ_99464 28578 RMVar_ID_28578 Human_SNP_ID_110716142 A-to-I Human chr2 - 207759613 207759613 207759613 TTTCGCTCTTGCCTCAGCCTCTTGCGTAGCTGAGATTACAGGCACGTGCCACCATGTCAGGCTAA TTTCGCTCTTGCCTCAGCCTCTTGCGTAGCTGGGATTACAGGCACGTGCCACCATGTCAGGCTAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1211480973 Functional Loss SNV dbSNP153 33..33 33 - - - 28579 RMVar_ID_28579 Human_SNP_ID_110772082 A-to-I Human chr2 - 207999596 207999596 207999596 TTCTTCTTTTAAAATCTGTTTTTTTAGGGACAAGGTCTTGTTGTCTCCCAGGCTGGAATATGATG TTCTTCTTTTAAAATCTGTTTTTTTAGGGACAGGGTCTTGTTGTCTCCCAGGCTGGAATATGATG T C PLEKHM3 Ensembl:ENSG00000178385 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1435766236 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71363,RMVar_hsa_circ_360030 28580 RMVar_ID_28580 Human_SNP_ID_110833937 A-to-I Human chr2 - 208237915 208237913 208237915 GTTTTTCTTTTTTTTTCTTTTTATTGAGACAGAGTCTCGCTTTGCCCAGGCTGGAGTGCAGTGGC GTTTTTCTTTTTTTTTCTTTTTATTGAGACAG__TCTCGCTTTGCCCAGGCTGGAGTGCAGTGGC ACT A IDH1 Ensembl:ENSG00000138413 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1409794206 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_17570989 RMVar_hsa_circ_128027,RMVar_hsa_circ_206434,RMVar_hsa_circ_104037,RMVar_hsa_circ_206433 28581 RMVar_ID_28581 Human_SNP_ID_110851101 A-to-I Human chr2 + 208308732 208308723 208308733 TAGTAGTTGGTTTTTTTTTTTTTTTGAGACGAAATTTTGCTCTTATTGTCCAGGCTGGAGTGCAA TAGTAGTTGGTTTTTTTTTTTTTT__________TTTTGCTCTTATTGTCCAGGCTGGAGTGCAA TTGAGACGAAA T PIKFYVE Ensembl:ENSG00000115020 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1326570297 Functional Loss DEL dbSNP153 25..34 33 - - - Human_RBP_ID_23851016 RMVar_hsa_circ_17777,RMVar_hsa_circ_366094,RMVar_hsa_circ_82083,RMVar_hsa_circ_30594,RMVar_hsa_circ_340955,RMVar_hsa_circ_115147,RMVar_hsa_circ_29753,RMVar_hsa_circ_206447,RMVar_hsa_circ_18092,RMVar_hsa_circ_206448,RMVar_hsa_circ_88827,RMVar_hsa_circ_93502,RMVar_hsa_circ_50472,RMVar_hsa_circ_206454,RMVar_hsa_circ_206455,RMVar_hsa_circ_59158,RMVar_hsa_circ_340130,RMVar_hsa_circ_375653,RMVar_hsa_circ_46782,RMVar_hsa_circ_206458,RMVar_hsa_circ_80683,RMVar_hsa_circ_206457,RMVar_hsa_circ_60422 28582 RMVar_ID_28582 Human_SNP_ID_110851108 A-to-I Human chr2 + 208308732 208308732 208308732 TAGTAGTTGGTTTTTTTTTTTTTTTGAGACGAAATTTTGCTCTTATTGTCCAGGCTGGAGTGCAA TAGTAGTTGGTTTTTTTTTTTTTTTGAGACGATATTTTGCTCTTATTGTCCAGGCTGGAGTGCAA A T PIKFYVE Ensembl:ENSG00000115020 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1470324841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23851016 RMVar_hsa_circ_17777,RMVar_hsa_circ_366094,RMVar_hsa_circ_82083,RMVar_hsa_circ_30594,RMVar_hsa_circ_340955,RMVar_hsa_circ_115147,RMVar_hsa_circ_29753,RMVar_hsa_circ_206447,RMVar_hsa_circ_18092,RMVar_hsa_circ_206448,RMVar_hsa_circ_88827,RMVar_hsa_circ_93502,RMVar_hsa_circ_50472,RMVar_hsa_circ_206454,RMVar_hsa_circ_206455,RMVar_hsa_circ_59158,RMVar_hsa_circ_340130,RMVar_hsa_circ_375653,RMVar_hsa_circ_46782,RMVar_hsa_circ_206458,RMVar_hsa_circ_80683,RMVar_hsa_circ_206457,RMVar_hsa_circ_60422 28583 RMVar_ID_28583 Human_SNP_ID_110854542 A-to-I Human chr2 + 208322111 208322111 208322111 TAACCATACTAAAACAACTTAGGGATGGGCATAGTGGCTGACACTTGTGATTACACTTTTGGAGC TAACCATACTAAAACAACTTAGGGATGGGCATGGTGGCTGACACTTGTGATTACACTTTTGGAGC A G PIKFYVE Ensembl:ENSG00000115020 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1211636122 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13757166 RMVar_hsa_circ_17777,RMVar_hsa_circ_82083,RMVar_hsa_circ_30594,RMVar_hsa_circ_115147,RMVar_hsa_circ_206447,RMVar_hsa_circ_206448,RMVar_hsa_circ_88827,RMVar_hsa_circ_93502,RMVar_hsa_circ_206454,RMVar_hsa_circ_206455,RMVar_hsa_circ_59158,RMVar_hsa_circ_340130,RMVar_hsa_circ_375653,RMVar_hsa_circ_32169,RMVar_hsa_circ_206457,RMVar_hsa_circ_60422,RMVar_hsa_circ_361533,RMVar_hsa_circ_378611,RMVar_hsa_circ_330367,RMVar_hsa_circ_206460,RMVar_hsa_circ_206459,RMVar_hsa_circ_70333,RMVar_hsa_circ_33543,RMVar_hsa_circ_357026 28584 RMVar_ID_28584 Human_SNP_ID_111071312 A-to-I Human chr2 + 209178890 209178888 209178890 AAGGAAGCTAAGCGGTTCTTCAGTAAATCCTCAGTTACCTCAGCAGCTGCATTAAGTGCATTGGC AAGGAAGCTAAGCGGTTCTTCAGTAAATCCT__GTTACCTCAGCAGCTGCATTAAGTGCATTGGC TCA T MEAF6P1 Ensembl:ENSG00000240286 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs966764333 Functional Loss DEL dbSNP153 32..33 33 - - - Human_miRNA_ID_1823572,Human_miRNA_ID_1884620 28585 RMVar_ID_28585 Human_SNP_ID_111071313 A-to-I Human chr2 + 209178890 209178890 209178890 AAGGAAGCTAAGCGGTTCTTCAGTAAATCCTCAGTTACCTCAGCAGCTGCATTAAGTGCATTGGC AAGGAAGCTAAGCGGTTCTTCAGTAAATCCTCGGTTACCTCAGCAGCTGCATTAAGTGCATTGGC A G MEAF6P1 Ensembl:ENSG00000240286 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1272151174 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1823572,Human_miRNA_ID_1884620 28586 RMVar_ID_28586 Human_SNP_ID_111071738 A-to-I Human chr2 + 209180513 209180513 209180513 GCCCTGGCCAACTCGGGAGGCATAAAGAAACTAGTGAACATAACCAAAGGCAGGGGCGACAGATC GCCCTGGCCAACTCGGGAGGCATAAAGAAACTGGTGAACATAACCAAAGGCAGGGGCGACAGATC A G PKP4P1,MEAF6P1 Ensembl:ENSG00000229670,Ensembl:ENSG00000240286 Pseudogene,Pseudogene exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404213805 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6961871 28587 RMVar_ID_28587 Human_SNP_ID_111071751 A-to-I Human chr2 + 209180558 209180558 209180558 AAAGGCAGGGGCGACAGATCATCTCTGAAAGTAGTGAAGGCAGTAGCCCAGGTCTTGAATACATT AAAGGCAGGGGCGACAGATCATCTCTGAAAGTGGTGAAGGCAGTAGCCCAGGTCTTGAATACATT A G PKP4P1,MEAF6P1 Ensembl:ENSG00000229670,Ensembl:ENSG00000240286 Pseudogene,Pseudogene exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1306614702 Functional Loss SNV dbSNP153 33..33 33 - - - 28588 RMVar_ID_28588 Human_SNP_ID_111071830 A-to-I Human chr2 + 209180812 209180812 209180812 ATATTCCTCACCAGCAAGAGAACTAAATAGACAGCTACAGCATCAACAGCTGTATTATAGTCAAG ATATTCCTCACCAGCAAGAGAACTAAATAGACGGCTACAGCATCAACAGCTGTATTATAGTCAAG A G PKP4P1,MEAF6P1 Ensembl:ENSG00000229670,Ensembl:ENSG00000240286 Pseudogene,Pseudogene exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1431219311 Functional Loss SNV dbSNP153 33..33 33 - - - 28589 RMVar_ID_28589 Human_SNP_ID_111071837 A-to-I Human chr2 + 209180847 209180847 209180847 TACAGCATCAACAGCTGTATTATAGTCAAGATAACTCCAACAAAATAACTTTGATTCATACAGAT TACAGCATCAACAGCTGTATTATAGTCAAGATGACTCCAACAAAATAACTTTGATTCATACAGAT A G PKP4P1,MEAF6P1 Ensembl:ENSG00000229670,Ensembl:ENSG00000240286 Pseudogene,Pseudogene exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1478534723 Functional Loss SNV dbSNP153 33..33 33 - - - 28590 RMVar_ID_28590 Human_SNP_ID_484066725 A-to-I Human chr11 + 120344167 120344167 120344167 ACATGCCTGTAATCCCAGCTACTCGGGAGGCTAAGACAGGAGAATCACTTGAACCCGGGAGGCGG ACATGCCTGTAATCCCAGCTACTCGGGAGGCTGAGACAGGAGAATCACTTGAACCCGGGAGGCGG A G ARHGEF12 Ensembl:ENSG00000196914 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1342980725 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_153570,RMVar_hsa_circ_119761 28591 RMVar_ID_28591 Human_SNP_ID_484070852 A-to-I Human chr11 + 120359431 120359431 120359431 TTTTTATTTATTTATTTATTTTTGGTAGAGATAGGGTTTTGCCATGTTGCCTAGGCTGGCCTCAA TTTTTATTTATTTATTTATTTTTGGTAGAGATGGGGTTTTGCCATGTTGCCTAGGCTGGCCTCAA A G ARHGEF12 Ensembl:ENSG00000196914 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs897740355 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_153570,RMVar_hsa_circ_119761 28592 RMVar_ID_28592 Human_SNP_ID_484072041 A-to-I Human chr11 + 120364926 120364926 120364926 CTGTAGCCTCAGCCTCTCAAGTAGCTGATACTACAGGCACACACCACCATGCTCAGCTAATTTTT CTGTAGCCTCAGCCTCTCAAGTAGCTGATACTGCAGGCACACACCACCATGCTCAGCTAATTTTT A G ARHGEF12 Ensembl:ENSG00000196914 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1243222456 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_153570,RMVar_hsa_circ_119761 28593 RMVar_ID_28593 Human_SNP_ID_484078744 A-to-I Human chr11 + 120394936 120394936 120394936 AAACATCAGCCGGCATTGTGGCGCGAACCTGTAATCCCAGCTACCTGGGAGGCTGAGGGATGAGA AAACATCAGCCGGCATTGTGGCGCGAACCTGTCATCCCAGCTACCTGGGAGGCTGAGGGATGAGA A C ARHGEF12 Ensembl:ENSG00000196914 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232672180 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_153570,RMVar_hsa_circ_119761 28594 RMVar_ID_28594 Human_SNP_ID_484078745 A-to-I Human chr11 + 120394936 120394936 120394936 AAACATCAGCCGGCATTGTGGCGCGAACCTGTAATCCCAGCTACCTGGGAGGCTGAGGGATGAGA AAACATCAGCCGGCATTGTGGCGCGAACCTGTGATCCCAGCTACCTGGGAGGCTGAGGGATGAGA A G ARHGEF12 Ensembl:ENSG00000196914 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232672180 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_153570,RMVar_hsa_circ_119761 28595 RMVar_ID_28595 Human_SNP_ID_484102153 A-to-I Human chr11 + 120493939 120493937 120493939 GGCTGAAATAATCCTGCCTCTGTCTCCCAAGTAGCTGGGAATACAGGCACGTGCCACCATGCCTG GGCTGAAATAATCCTGCCTCTGTCTCCCAAG__GCTGGGAATACAGGCACGTGCCACCATGCCTG GTA G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1376403728 Functional Loss DEL dbSNP153 32..33 33 - - - 28596 RMVar_ID_28596 Human_SNP_ID_484251519 A-to-I Human chr11 + 121121917 121121916 121121917 CACAGAACAATGGATAAGTGTTCAGCACTCTTACTAGCTGACCTTCCCTATAATATGGCTCTTCT CACAGAACAATGGATAAGTGTTCAGCACTCTT_CTAGCTGACCTTCCCTATAATATGGCTCTTCT TA T TECTA Ensembl:ENSG00000109927 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1219822179 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_327101,RMVar_hsa_circ_337245 28597 RMVar_ID_28597 Human_SNP_ID_484251521 A-to-I Human chr11 + 121121920 121121920 121121920 AGAACAATGGATAAGTGTTCAGCACTCTTACTAGCTGACCTTCCCTATAATATGGCTCTTCTCTC AGAACAATGGATAAGTGTTCAGCACTCTTACTGGCTGACCTTCCCTATAATATGGCTCTTCTCTC A G TECTA Ensembl:ENSG00000109927 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1268625214 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_327101,RMVar_hsa_circ_337245 28598 RMVar_ID_28598 Human_SNP_ID_484298217 A-to-I Human chr11 + 121312270 121312266 121312271 CAGGCTTTTGGTATGGGAAGAAAAATACTTATAAATACTTGTTTTAATATTTGCTTTATTAAAAT CAGGCTTTTGGTATGGGAAGAAAAATACT_____ATACTTGTTTTAATATTTGCTTTATTAAAAT TTATAA T SC5D Ensembl:ENSG00000109929 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1336787742 Functional Loss DEL dbSNP153 30..34 33 - - - Human_RBP_ID_18248349,Human_RBP_ID_27615491 28599 RMVar_ID_28599 Human_SNP_ID_484298220 A-to-I Human chr11 + 121312270 121312270 121312270 CAGGCTTTTGGTATGGGAAGAAAAATACTTATAAATACTTGTTTTAATATTTGCTTTATTAAAAT CAGGCTTTTGGTATGGGAAGAAAAATACTTATGAATACTTGTTTTAATATTTGCTTTATTAAAAT A G SC5D Ensembl:ENSG00000109929 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs755671934 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18248349,Human_RBP_ID_27615491 28600 RMVar_ID_28600 Human_SNP_ID_484523615 A-to-I Human chr11 - 122247909 122247909 122247909 ATCAAAATTCTTTGCACCTGGCTGGACGTGGTAGCTCACGCCTGTAATGCCACCACTTTGGGAGG ATCAAAATTCTTTGCACCTGGCTGGACGTGGTCGCTCACGCCTGTAATGCCACCACTTTGGGAGG T G MIR100HG Ensembl:ENSG00000255248 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1475654601 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_288329,RMVar_hsa_circ_363961,RMVar_hsa_circ_308149,RMVar_hsa_circ_360573 28601 RMVar_ID_28601 Human_SNP_ID_484610237 A-to-I Human chr11 - 122613980 122613980 122613980 AAGCTGGAGTCAAGATTGCAGGGACTAATGCCAAGGTCTTGCCTGCCCAGTGGGAATTTCAAATT AAGCTGGAGTCAAGATTGCAGGGACTAATGCCGAGGTCTTGCCTGCCCAGTGGGAATTTCAAATT T C GLULP3 Ensembl:ENSG00000254572 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1022121342 Functional Loss SNV dbSNP153 33..33 33 - - - 28602 RMVar_ID_28602 Human_SNP_ID_484624233 A-to-I Human chr11 + 122671316 122671316 122671316 GGGAGGATGAGGCAGGCAGATTGCTTAAGGCCAGGAGTTCAAGACTAGCCTAGGCAACATGGCAA GGGAGGATGAGGCAGGCAGATTGCTTAAGGCCGGGAGTTCAAGACTAGCCTAGGCAACATGGCAA A G UBASH3B Ensembl:ENSG00000154127 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1389213307 Functional Loss SNV dbSNP153 33..33 33 - - - 28603 RMVar_ID_28603 Human_SNP_ID_484636629 A-to-I Human chr11 + 122721194 122721194 122721194 TTGAACCCGGTGGTGGAGGTTTGCAGTGAGCCAAGATCGCGGCACTGCACTCCAGTCTGGGCAAC TTGAACCCGGTGGTGGAGGTTTGCAGTGAGCCGAGATCGCGGCACTGCACTCCAGTCTGGGCAAC A G UBASH3B Ensembl:ENSG00000154127 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs557430514 Functional Loss SNV dbSNP153 33..33 33 - - - 28604 RMVar_ID_28604 Human_SNP_ID_484709494 A-to-I Human chr11 - 123018184 123018184 123018184 TCAGGCCCATCTTCTACTCCTTGGCTAACTTTAGCAACTTTAGTTTTCTCCTCTACAAACTCATG TCAGGCCCATCTTCTACTCCTTGGCTAACTTTGGCAACTTTAGTTTTCTCCTCTACAAACTCATG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879082202 Functional Loss SNV dbSNP153 33..33 33 - - - 28605 RMVar_ID_28605 Human_SNP_ID_484725309 A-to-I Human chr11 - 123071554 123071554 123071554 ACACCCAGCTAATTTTTGGAGTTCTGATAGAGACAGGGTTTCTCCATGTTGGCCAGGCTTGTCTC ACACCCAGCTAATTTTTGGAGTTCTGATAGAGGCAGGGTTTCTCCATGTTGGCCAGGCTTGTCTC T C CLMP Ensembl:ENSG00000166250 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1229789092 Functional Loss SNV dbSNP153 33..33 33 - - - 28606 RMVar_ID_28606 Human_SNP_ID_484725484 A-to-I Human chr11 - 123072338 123072338 123072338 TGCCATTGCACTCCAGCCTGGGTGACAAAGCAAGACTCCATCTCAAAAAAAAAAAAAAATCAAGG TGCCATTGCACTCCAGCCTGGGTGACAAAGCAGGACTCCATCTCAAAAAAAAAAAAAAATCAAGG T C CLMP Ensembl:ENSG00000166250 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs150388532 Functional Loss SNV dbSNP153 33..33 33 - - - 28607 RMVar_ID_28607 Human_SNP_ID_484725485 A-to-I Human chr11 - 123072338 123072338 123072338 TGCCATTGCACTCCAGCCTGGGTGACAAAGCAAGACTCCATCTCAAAAAAAAAAAAAAATCAAGG TGCCATTGCACTCCAGCCTGGGTGACAAAGCACGACTCCATCTCAAAAAAAAAAAAAAATCAAGG T G CLMP Ensembl:ENSG00000166250 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs150388532 Functional Loss SNV dbSNP153 33..33 33 - - - 28608 RMVar_ID_28608 Human_SNP_ID_484725495 A-to-I Human chr11 - 123072376 123072376 123072376 AAAATCCAGCAGGTGGAGGTTGCAGTGAGCCAAGATTATGCCATTGCACTCCAGCCTGGGTGACA AAAATCCAGCAGGTGGAGGTTGCAGTGAGCCATGATTATGCCATTGCACTCCAGCCTGGGTGACA T A CLMP Ensembl:ENSG00000166250 Protein coding 3'UTR GSE47997;GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831 K562 cells&HepG2 cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line - 23474544,29129909,32596459 RNA-Seq:(High) rs562335495 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11549386 28609 RMVar_ID_28609 Human_SNP_ID_484727285 A-to-I Human chr11 - 123078917 123078917 123078917 AAAACTTGCCGGGCACGGTGACTCACGCCTATAATCCCAGCACTTTGGGAGGCCGAGGCAGGTGG AAAACTTGCCGGGCACGGTGACTCACGCCTATGATCCCAGCACTTTGGGAGGCCGAGGCAGGTGG T C CLMP Ensembl:ENSG00000166250 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941416305 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18586 28610 RMVar_ID_28610 Human_SNP_ID_484744420 A-to-I Human chr11 - 123144480 123144480 123144480 GTAATGCCAGCTACTCAGGAAGCTGAGACAGGAGAATCGCTTGAACCCAGGAGGCGGAGGTTGCA GTAATGCCAGCTACTCAGGAAGCTGAGACAGGCGAATCGCTTGAACCCAGGAGGCGGAGGTTGCA T G CLMP Ensembl:ENSG00000166250 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs533589109 Functional Loss SNV dbSNP153 33..33 33 - - - 28611 RMVar_ID_28611 Human_SNP_ID_484751822 A-to-I Human chr11 - 123173890 123173890 123173890 TCTTGTAGAGATGAGATTTCACCATATTGCCCAGGCTGGTCTCGAACTCCTGAGCTCAAGCGATC TCTTGTAGAGATGAGATTTCACCATATTGCCCCGGCTGGTCTCGAACTCCTGAGCTCAAGCGATC T G CLMP Ensembl:ENSG00000166250 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1403559266 Functional Loss SNV dbSNP153 33..33 33 - - - 28612 RMVar_ID_28612 Human_SNP_ID_484751825 A-to-I Human chr11 - 123173897 123173897 123173897 TTGGATTTCTTGTAGAGATGAGATTTCACCATATTGCCCAGGCTGGTCTCGAACTCCTGAGCTCA TTGGATTTCTTGTAGAGATGAGATTTCACCATGTTGCCCAGGCTGGTCTCGAACTCCTGAGCTCA T C CLMP Ensembl:ENSG00000166250 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223416439 Functional Loss SNV dbSNP153 33..33 33 - - - 28613 RMVar_ID_28613 Human_SNP_ID_484751826 A-to-I Human chr11 - 123173899 123173899 123173899 TTTTGGATTTCTTGTAGAGATGAGATTTCACCATATTGCCCAGGCTGGTCTCGAACTCCTGAGCT TTTTGGATTTCTTGTAGAGATGAGATTTCACCGTATTGCCCAGGCTGGTCTCGAACTCCTGAGCT T C CLMP Ensembl:ENSG00000166250 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1469107528 Functional Loss SNV dbSNP153 33..33 33 - - - 28614 RMVar_ID_28614 Human_SNP_ID_484833013 A-to-I Human chr11 + 123500156 123500156 123500156 TAGCCTGGCCAACGTGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCTGGGCGTGGTTG TAGCCTGGCCAACGTGGTGAAACCCCGTCTCTGCTAAAAATACAAAAATTAGCTGGGCGTGGTTG A G GRAMD1B Ensembl:ENSG00000023171 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs929267349 Functional Loss SNV dbSNP153 33..33 33 - - - 28615 RMVar_ID_28615 Human_SNP_ID_484848737 A-to-I Human chr11 + 123565065 123565065 123565065 TCATATTTTATTTTATTTTGAGAAAGGATCTCACTCTGTTGACTAGGCTGAAGTGTAGTGGTGTG TCATATTTTATTTTATTTTGAGAAAGGATCTCCCTCTGTTGACTAGGCTGAAGTGTAGTGGTGTG A C GRAMD1B Ensembl:ENSG00000023171 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs552371264 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77125,RMVar_hsa_circ_153797 28616 RMVar_ID_28616 Human_SNP_ID_484848738 A-to-I Human chr11 + 123565065 123565065 123565065 TCATATTTTATTTTATTTTGAGAAAGGATCTCACTCTGTTGACTAGGCTGAAGTGTAGTGGTGTG TCATATTTTATTTTATTTTGAGAAAGGATCTCGCTCTGTTGACTAGGCTGAAGTGTAGTGGTGTG A G GRAMD1B Ensembl:ENSG00000023171 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs552371264 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77125,RMVar_hsa_circ_153797 28617 RMVar_ID_28617 Human_SNP_ID_484857396 A-to-I Human chr11 - 123598448 123598448 123598448 GCCCAAATCTATGAATACGTAGAGATTCTCGGAGAACAGCGACATCTCACTCATGAAAATGTACA GCCCAAATCTATGAATACGTAGAGATTCTCGGGGAACAGCGACATCTCACTCATGAAAATGTACA T C SF3A3P2 Ensembl:ENSG00000254449 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1242304376 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8246773,Human_RBP_ID_17351050,Human_RBP_ID_18526082,Human_RBP_ID_26410339 28618 RMVar_ID_28618 Human_SNP_ID_484857532 A-to-I Human chr11 - 123599054 123599054 123599054 GAGGCACAAAACTCGGTGGAGTTCACAGATGAAGAGGGATATGGTCGTTACCTCGATCTCCATGA GAGGCACAAAACTCGGTGGAGTTCACAGATGAGGAGGGATATGGTCGTTACCTCGATCTCCATGA T C SF3A3P2 Ensembl:ENSG00000254449 Pseudogene exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs879010397 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18526187 28619 RMVar_ID_28619 Human_SNP_ID_484862133 A-to-I Human chr11 + 123617242 123617242 123617242 TTCTCACTCTGTTGCCCAGGCTGGAATGCAGTAGCATGATCTCAGCTCACTCTAACTTCCCCTTC TTCTCACTCTGTTGCCCAGGCTGGAATGCAGTTGCATGATCTCAGCTCACTCTAACTTCCCCTTC A T GRAMD1B Ensembl:ENSG00000023171 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1242842930 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14139,RMVar_hsa_circ_6932,RMVar_hsa_circ_303637 28620 RMVar_ID_28620 Human_SNP_ID_485138814 A-to-I Human chr11 - 124757239 124757239 124757239 TTTTGTAGAGACTGTGTTTCACCGTATTGCCCAGGCTGGTCTTGAACTCTTGGACTCAAGCAATC TTTTGTAGAGACTGTGTTTCACCGTATTGCCCTGGCTGGTCTTGAACTCTTGGACTCAAGCAATC T A ESAM Ensembl:ENSG00000149564 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs868175902 Functional Loss SNV dbSNP153 33..33 33 - - - 28621 RMVar_ID_28621 Human_SNP_ID_485138979 A-to-I Human chr11 - 124757835 124757835 124757835 AAATTAGTCGGACATGGTGGCACCCGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAAGAGAA AAATTAGTCGGACATGGTGGCACCCGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAAGAGAA T C ESAM Ensembl:ENSG00000149564 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1302545564 Functional Loss SNV dbSNP153 33..33 33 - - - 28622 RMVar_ID_28622 Human_SNP_ID_485303053 A-to-I Human chr11 + 125416192 125416192 125416192 GGGCGTGGTGGCGGGCGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATGGCGTGAA GGGCGTGGTGGCGGGCGCCTGTAGTCCCAGCTGCTTGGGAGGCTGAGGCAGGAGAATGGCGTGAA A G PKNOX2 Ensembl:ENSG00000165495 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs550007905 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_111529 28623 RMVar_ID_28623 Human_SNP_ID_485341519 A-to-I Human chr11 + 125579450 125579450 125579450 CACTTTGGGAGGCCGAGGTGGGCGGATCACCTAAGGTCAGGCATTTGAGACCAGCCTGGCCAACA CACTTTGGGAGGCCGAGGTGGGCGGATCACCTTAGGTCAGGCATTTGAGACCAGCCTGGCCAACA A T EI24 Ensembl:ENSG00000149547 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1484466591 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_308730,RMVar_hsa_circ_4281,RMVar_hsa_circ_347640,RMVar_hsa_circ_28318,RMVar_hsa_circ_279928,RMVar_hsa_circ_153856 28624 RMVar_ID_28624 Human_SNP_ID_485346396 A-to-I Human chr11 + 125598065 125598065 125598065 AAAACCCCATCTCTACTAAAAATACAAAAATTAGCTGGGCATGGTGGCATGTGCCCGTAATCCCA AAAACCCCATCTCTACTAAAAATACAAAAATTGGCTGGGCATGGTGGCATGTGCCCGTAATCCCA A G STT3A Ensembl:ENSG00000134910 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs879351830 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7023,RMVar_hsa_circ_314750,RMVar_hsa_circ_331445,RMVar_hsa_circ_374872,RMVar_hsa_circ_126799,RMVar_hsa_circ_59067,RMVar_hsa_circ_49708,RMVar_hsa_circ_86425,RMVar_hsa_circ_153859,RMVar_hsa_circ_153861,RMVar_hsa_circ_153862,RMVar_hsa_circ_153860,RMVar_hsa_circ_374600,RMVar_hsa_circ_309493,RMVar_hsa_circ_72189,RMVar_hsa_circ_153864,RMVar_hsa_circ_20816,RMVar_hsa_circ_153865,RMVar_hsa_circ_153863 28625 RMVar_ID_28625 Human_SNP_ID_485350394 A-to-I Human chr11 + 125615074 125615074 125615074 AAGGCGGGCGGATCACTTGAGGTCAGGAGTTCATGACCAGCCTGGGCAACATAGTGAAACCTTGT AAGGCGGGCGGATCACTTGAGGTCAGGAGTTCTTGACCAGCCTGGGCAACATAGTGAAACCTTGT A T STT3A Ensembl:ENSG00000134910 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1310547916 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_374872,RMVar_hsa_circ_153862,RMVar_hsa_circ_20816,RMVar_hsa_circ_153866,RMVar_hsa_circ_79993,RMVar_hsa_circ_88712,RMVar_hsa_circ_153872,RMVar_hsa_circ_315208,RMVar_hsa_circ_83565,RMVar_hsa_circ_95222,RMVar_hsa_circ_153879,RMVar_hsa_circ_153880,RMVar_hsa_circ_115884,RMVar_hsa_circ_123820,RMVar_hsa_circ_153884,RMVar_hsa_circ_153885,RMVar_hsa_circ_12465,RMVar_hsa_circ_366662,RMVar_hsa_circ_109089,RMVar_hsa_circ_1235,RMVar_hsa_circ_153889,RMVar_hsa_circ_119699,RMVar_hsa_circ_153890,RMVar_hsa_circ_153891 28626 RMVar_ID_28626 Human_SNP_ID_485350758 A-to-I Human chr11 + 125616817 125616817 125616817 TTCCCACCTCAGCCTCCTGAGTAGCTGGGACTACAGGCACACACCACCATGCCCGGCCAATTTTT TTCCCACCTCAGCCTCCTGAGTAGCTGGGACTGCAGGCACACACCACCATGCCCGGCCAATTTTT A G STT3A Ensembl:ENSG00000134910 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs964807874 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_374872,RMVar_hsa_circ_153862,RMVar_hsa_circ_20816,RMVar_hsa_circ_153866,RMVar_hsa_circ_79993,RMVar_hsa_circ_88712,RMVar_hsa_circ_153872,RMVar_hsa_circ_315208,RMVar_hsa_circ_83565,RMVar_hsa_circ_95222,RMVar_hsa_circ_153879,RMVar_hsa_circ_153880,RMVar_hsa_circ_115884,RMVar_hsa_circ_123820,RMVar_hsa_circ_153884,RMVar_hsa_circ_153885,RMVar_hsa_circ_12465,RMVar_hsa_circ_366662,RMVar_hsa_circ_109089,RMVar_hsa_circ_1235,RMVar_hsa_circ_153889,RMVar_hsa_circ_119699,RMVar_hsa_circ_153890,RMVar_hsa_circ_153891 28627 RMVar_ID_28627 Human_SNP_ID_485357374 A-to-I Human chr11 - 125643850 125643850 125643850 GGAGAGAAGTCCAAATTGGATTGAATGTGCTTAGAAAATCCACTGGGAGACTCTGACACACCACC GGAGAGAAGTCCAAATTGGATTGAATGTGCTTTGAAAATCCACTGGGAGACTCTGACACACCACC T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1024169258 Functional Loss SNV dbSNP153 33..33 33 - - - 28628 RMVar_ID_28628 Human_SNP_ID_485366600 A-to-I Human chr11 + 125683180 125683180 125683180 AGTCGGGCATGGTGGCGGGCACCTGCAATTCCAGCTACTTGGGAGGCGAAGGCAGGAGAATCGCT AGTCGGGCATGGTGGCGGGCACCTGCAATTCCGGCTACTTGGGAGGCGAAGGCAGGAGAATCGCT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946742644 Functional Loss SNV dbSNP153 33..33 33 - - - 28629 RMVar_ID_28629 Human_SNP_ID_485463130 A-to-I Human chr11 - 126067522 126067522 126067522 ATCAAGTTCAGATTGTCAGTGTCTGCCATGTTATAAGAACTCCAAATATCGGCAGCTAGTATGGG ATCAAGTTCAGATTGTCAGTGTCTGCCATGTTTTAAGAACTCCAAATATCGGCAGCTAGTATGGG T A - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs112433340 Functional Loss SNV dbSNP153 33..33 33 - - - 28630 RMVar_ID_28630 Human_SNP_ID_485463131 A-to-I Human chr11 - 126067522 126067522 126067522 ATCAAGTTCAGATTGTCAGTGTCTGCCATGTTATAAGAACTCCAAATATCGGCAGCTAGTATGGG ATCAAGTTCAGATTGTCAGTGTCTGCCATGTTGTAAGAACTCCAAATATCGGCAGCTAGTATGGG T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs112433340 Functional Loss SNV dbSNP153 33..33 33 - - - 28631 RMVar_ID_28631 Human_SNP_ID_485463268 A-to-I Human chr11 + 126068139 126068139 126068139 GAAAGATACTAAAGTGAAGCTCTCAGATGCTGACCAGCCTATGAATTTTGTCTTAGAATTTCACT GAAAGATACTAAAGTGAAGCTCTCAGATGCTGGCCAGCCTATGAATTTTGTCTTAGAATTTCACT A G NAP1L1P1 Ensembl:ENSG00000254759 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs907826603 Functional Loss SNV dbSNP153 33..33 33 - - - 28632 RMVar_ID_28632 Human_SNP_ID_485492139 A-to-I Human chr11 - 126182547 126182547 126182547 AGGAGGCTAAGGTGGGAGGATTGCTTGAGCCCAGGAGGCTGAGGCTGCAGTGAGCCATGATCACC AGGAGGCTAAGGTGGGAGGATTGCTTGAGCCCGGGAGGCTGAGGCTGCAGTGAGCCATGATCACC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs556430198 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_153933 28633 RMVar_ID_28633 Human_SNP_ID_485492180 A-to-I Human chr11 - 126182658 126182658 126182658 TGGCATCCAGGAATTAGAGATCATTCTGGGCAACACAGTGAGACTCTATCTCTACAAAAAACAAA TGGCATCCAGGAATTAGAGATCATTCTGGGCAGCACAGTGAGACTCTATCTCTACAAAAAACAAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1303085560 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11553846 RMVar_hsa_circ_153933 28634 RMVar_ID_28634 Human_SNP_ID_485498756 A-to-I Human chr11 - 126207776 126207776 126207776 GGAGGGCAGTGGCACAATCTTGGCTCACTGCAACCTCCTCCCTGGTTCAAGTGGTTCTCATGTTT GGAGGGCAGTGGCACAATCTTGGCTCACTGCAGCCTCCTCCCTGGTTCAAGTGGTTCTCATGTTT T C RPUSD4 Ensembl:ENSG00000165526 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1013100826 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66073,RMVar_hsa_circ_104908,RMVar_hsa_circ_153938 28635 RMVar_ID_28635 Human_SNP_ID_485498759 A-to-I Human chr11 - 126207782 126207782 126207782 CAGGCTGGAGGGCAGTGGCACAATCTTGGCTCACTGCAACCTCCTCCCTGGTTCAAGTGGTTCTC CAGGCTGGAGGGCAGTGGCACAATCTTGGCTCGCTGCAACCTCCTCCCTGGTTCAAGTGGTTCTC T C RPUSD4 Ensembl:ENSG00000165526 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1436844664 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66073,RMVar_hsa_circ_104908,RMVar_hsa_circ_153938 28636 RMVar_ID_28636 Human_SNP_ID_485499173 A-to-I Human chr11 - 126209217 126209217 126209217 AGAGGCAGAGGTGGGAGGATCACTTTAGGCCAAGAGTCGGAGAACAGCCTGGGCAACATAGTGAC AGAGGCAGAGGTGGGAGGATCACTTTAGGCCAGGAGTCGGAGAACAGCCTGGGCAACATAGTGAC T C RPUSD4 Ensembl:ENSG00000165526 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs549189247 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11554490 RMVar_hsa_circ_66073,RMVar_hsa_circ_104908,RMVar_hsa_circ_153938 28637 RMVar_ID_28637 Human_SNP_ID_485499174 A-to-I Human chr11 - 126209217 126209217 126209217 AGAGGCAGAGGTGGGAGGATCACTTTAGGCCAAGAGTCGGAGAACAGCCTGGGCAACATAGTGAC AGAGGCAGAGGTGGGAGGATCACTTTAGGCCACGAGTCGGAGAACAGCCTGGGCAACATAGTGAC T G RPUSD4 Ensembl:ENSG00000165526 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs549189247 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11554490 RMVar_hsa_circ_66073,RMVar_hsa_circ_104908,RMVar_hsa_circ_153938 28638 RMVar_ID_28638 Human_SNP_ID_485515605 A-to-I Human chr11 + 126272025 126272025 126272025 GCTCTGTCACCCAGGCTGGAGTGCAATGGCACAATCTCAGCTCACTGCAACCTCCACCTCCCAGG GCTCTGTCACCCAGGCTGGAGTGCAATGGCACCATCTCAGCTCACTGCAACCTCCACCTCCCAGG A C FOXRED1 Ensembl:ENSG00000110074 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1015836997 Functional Loss SNV dbSNP153 33..33 33 - - - 28639 RMVar_ID_28639 Human_SNP_ID_485515619 A-to-I Human chr11 + 126272091 126272091 126272091 TCAAGTGATTATCCCACCTCCGCCCCCTGAGTAGCTGAGATTACAGGGACACACCCTGATGCCCA TCAAGTGATTATCCCACCTCCGCCCCCTGAGTTGCTGAGATTACAGGGACACACCCTGATGCCCA A T FOXRED1 Ensembl:ENSG00000110074 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs561952699 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11555065 28640 RMVar_ID_28640 Human_SNP_ID_485515620 A-to-I Human chr11 + 126272096 126272096 126272096 TGATTATCCCACCTCCGCCCCCTGAGTAGCTGAGATTACAGGGACACACCCTGATGCCCAGCTAT TGATTATCCCACCTCCGCCCCCTGAGTAGCTGCGATTACAGGGACACACCCTGATGCCCAGCTAT A C FOXRED1 Ensembl:ENSG00000110074 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs980516848 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11555065 28641 RMVar_ID_28641 Human_SNP_ID_485515628 A-to-I Human chr11 + 126272127 126272127 126272127 GAGATTACAGGGACACACCCTGATGCCCAGCTATTTTTTGTATTTTTAGTAGAGATGAGGTTTCA GAGATTACAGGGACACACCCTGATGCCCAGCTGTTTTTTGTATTTTTAGTAGAGATGAGGTTTCA A G FOXRED1 Ensembl:ENSG00000110074 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1565352450 Functional Loss SNV dbSNP153 33..33 33 - - - 28642 RMVar_ID_28642 Human_SNP_ID_485519172 A-to-I Human chr11 + 126284236 126284236 126284236 TTGCATTTTCAGTAGCGACGGGGTTTCGCCATATTGGCCAGGGTGGTCTCGAACTCCTGAACTCA TTGCATTTTCAGTAGCGACGGGGTTTCGCCATCTTGGCCAGGGTGGTCTCGAACTCCTGAACTCA A C TIRAP Ensembl:ENSG00000150455 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs932893422 Functional Loss SNV dbSNP153 33..33 33 - - - 28643 RMVar_ID_28643 Human_SNP_ID_485519174 A-to-I Human chr11 + 126284243 126284243 126284243 TTCAGTAGCGACGGGGTTTCGCCATATTGGCCAGGGTGGTCTCGAACTCCTGAACTCAGGTGATC TTCAGTAGCGACGGGGTTTCGCCATATTGGCCTGGGTGGTCTCGAACTCCTGAACTCAGGTGATC A T TIRAP Ensembl:ENSG00000150455 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355497641 Functional Loss SNV dbSNP153 33..33 33 - - - 28644 RMVar_ID_28644 Human_SNP_ID_485521948 A-to-I Human chr11 + 126294840 126294840 126294840 CTATTTTGCCAGGCGCCATGGCTCACACCTGTAATCTCAGCACTTTGGGAGGCCGAGGCAGGTGG CTATTTTGCCAGGCGCCATGGCTCACACCTGTTATCTCAGCACTTTGGGAGGCCGAGGCAGGTGG A T TIRAP Ensembl:ENSG00000150455 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1178971291 Functional Loss SNV dbSNP153 33..33 33 - - - 28645 RMVar_ID_28645 Human_SNP_ID_485521985 A-to-I Human chr11 + 126294947 126294947 126294947 GTGAAACCCTGTCTCTACTAAAAAAACAAAAAAAATCAGCTGGGTGTGGTGGCGGGGGCCTGTAG GTGAAACCCTGTCTCTACTAAAAAAACAAAAACAATCAGCTGGGTGTGGTGGCGGGGGCCTGTAG A C TIRAP Ensembl:ENSG00000150455 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs948048456 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6053920 28646 RMVar_ID_28646 Human_SNP_ID_485521986 A-to-I Human chr11 + 126294947 126294947 126294947 GTGAAACCCTGTCTCTACTAAAAAAACAAAAAAAATCAGCTGGGTGTGGTGGCGGGGGCCTGTAG GTGAAACCCTGTCTCTACTAAAAAAACAAAAAGAATCAGCTGGGTGTGGTGGCGGGGGCCTGTAG A G TIRAP Ensembl:ENSG00000150455 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs948048456 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6053920 28647 RMVar_ID_28647 Human_SNP_ID_485522094 A-to-I Human chr11 + 126295346 126295346 126295346 GGGAGGCAGAAGTTGCAGTGAGCCGATATTGCACCACCGCACTCCAGCCTGGGTGACAGAGTGAG GGGAGGCAGAAGTTGCAGTGAGCCGATATTGCCCCACCGCACTCCAGCCTGGGTGACAGAGTGAG A C TIRAP Ensembl:ENSG00000150455 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1461105314 Functional Loss SNV dbSNP153 33..33 33 - - - 28648 RMVar_ID_28648 Human_SNP_ID_485522217 A-to-I Human chr11 + 126295897 126295897 126295897 GCCTCTGAACTTTTTTGTACATTTTCACAAGCAAGATTTTCTAGGATTTAGCCTAGAAAATCCTG GCCTCTGAACTTTTTTGTACATTTTCACAAGCGAGATTTTCTAGGATTTAGCCTAGAAAATCCTG A G TIRAP Ensembl:ENSG00000150455 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1032915750 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6053923,Human_RBP_ID_17791930 28649 RMVar_ID_28649 Human_SNP_ID_485522421 A-to-I Human chr11 + 126296817 126296817 126296817 GGGATTACAGGCATGCACCACCACACCCGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCA GGGATTACAGGCATGCACCACCACACCCGGCTCATTTTTGTATTTTTAGTAGAGATGGGGTTTCA A C TIRAP Ensembl:ENSG00000150455 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs972372174 Functional Loss SNV dbSNP153 33..33 33 - - - 28650 RMVar_ID_28650 Human_SNP_ID_485522425 A-to-I Human chr11 + 126296832 126296832 126296832 CACCACCACACCCGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATATTGGCCAGGC CACCACCACACCCGGCTAATTTTTGTATTTTTGGTAGAGATGGGGTTTCACCATATTGGCCAGGC A G TIRAP Ensembl:ENSG00000150455 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1024456720 Functional Loss SNV dbSNP153 33..33 33 - - - 28651 RMVar_ID_28651 Human_SNP_ID_485522427 A-to-I Human chr11 + 126296835 126296835 126296835 CACCACACCCGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATATTGGCCAGGCTAG CACCACACCCGGCTAATTTTTGTATTTTTAGTGGAGATGGGGTTTCACCATATTGGCCAGGCTAG A G TIRAP Ensembl:ENSG00000150455 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1460878822 Functional Loss SNV dbSNP153 33..33 33 - - - 28652 RMVar_ID_28652 Human_SNP_ID_485522447 A-to-I Human chr11 + 126296913 126296913 126296913 ACTTCAGGTGATCCACCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAAGCACCACGC ACTTCAGGTGATCCACCTGCCTCGGCCTCCCAGAGTGCTGGGATTACAGGCGTGAAGCACCACGC A G TIRAP Ensembl:ENSG00000150455 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs537425009 Functional Loss SNV dbSNP153 33..33 33 - - - 28653 RMVar_ID_28653 Human_SNP_ID_485522645 A-to-I Human chr11 + 126297856 126297856 126297856 TCGACCTCCTGGGCCCAAGCAATGATTCTCCTATCTCAGCCCTCTGAGTAGCTGGGACCACAGGC TCGACCTCCTGGGCCCAAGCAATGATTCTCCTGTCTCAGCCCTCTGAGTAGCTGGGACCACAGGC A G TIRAP Ensembl:ENSG00000150455 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1337885079 Functional Loss SNV dbSNP153 33..33 33 - - - 28654 RMVar_ID_28654 Human_SNP_ID_485522779 A-to-I Human chr11 + 126298406 126298404 126298407 GTGCGTGTCACCACACCCAGATAATTTTTTGTATTTTTAGTAGCGATAGGGTTTCACCGTGTTAG GTGCGTGTCACCACACCCAGATAATTTTTTG___TTTTAGTAGCGATAGGGTTTCACCGTGTTAG GTAT G TIRAP Ensembl:ENSG00000150455 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1256460522 Functional Loss DEL dbSNP153 32..34 33 - - - 28655 RMVar_ID_28655 Human_SNP_ID_485522834 A-to-I Human chr11 + 126298656 126298656 126298656 ATTCTGGTTTTTTTGAGACGGAGTCTTGCCCTATTGCCCAGGCCGGAGTGCAGTGGGATTACACG ATTCTGGTTTTTTTGAGACGGAGTCTTGCCCTTTTGCCCAGGCCGGAGTGCAGTGGGATTACACG A T TIRAP Ensembl:ENSG00000150455 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs998936177 Functional Loss SNV dbSNP153 33..33 33 - - - 28656 RMVar_ID_28656 Human_SNP_ID_485534950 A-to-I Human chr11 + 126346624 126346624 126346624 GCATCATGCTGCCAGAGGGGCTGGTGTTTGCCACTTTGTCAGAGTAGGGCTGTGGATTTTGTGCC GCATCATGCTGCCAGAGGGGCTGGTGTTTGCCGCTTTGTCAGAGTAGGGCTGTGGATTTTGTGCC A G DCPS Ensembl:ENSG00000110063 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1422855932 Functional Loss SNV dbSNP153 33..33 33 - - - 28657 RMVar_ID_28657 Human_SNP_ID_485534962 A-to-I Human chr11 + 126346706 126346706 126346706 AGGGATGGCAGGATGGCAGGCTCCTAAGTGACAGCAGGGGGGAAGCTTGAGGCACAGTGGGTGGT AGGGATGGCAGGATGGCAGGCTCCTAAGTGACTGCAGGGGGGAAGCTTGAGGCACAGTGGGTGGT A T DCPS Ensembl:ENSG00000110063 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs186922208 Functional Loss SNV dbSNP153 33..33 33 - - - 28658 RMVar_ID_28658 Human_SNP_ID_485535052 A-to-I Human chr11 + 126346967 126346967 126346967 GAAAAATTAGCCAGGTGTGGTGGTGGGCTCCTATAATCCCACCTACTTGGGAGGCTGAAGCAGGA GAAAAATTAGCCAGGTGTGGTGGTGGGCTCCTGTAATCCCACCTACTTGGGAGGCTGAAGCAGGA A G DCPS Ensembl:ENSG00000110063 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1333911056 Functional Loss SNV dbSNP153 33..33 33 - - - 28659 RMVar_ID_28659 Human_SNP_ID_485535661 A-to-I Human chr11 + 126349096 126349096 126349096 GCCTCCTGGATCTCACGCAGGGGATGGAGAGTAAGGACCAGCCCCTCTACCTCATGCTTTCTTCC GCCTCCTGGATCTCACGCAGGGGATGGAGAGTGAGGACCAGCCCCTCTACCTCATGCTTTCTTCC A G DCPS Ensembl:ENSG00000110063 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1268491032 Functional Loss SNV dbSNP153 33..33 33 - - - 28660 RMVar_ID_28660 Human_SNP_ID_485535664 A-to-I Human chr11 + 126349112 126349112 126349112 GCAGGGGATGGAGAGTAAGGACCAGCCCCTCTACCTCATGCTTTCTTCCTGCTATCTCGTAAGAG GCAGGGGATGGAGAGTAAGGACCAGCCCCTCTGCCTCATGCTTTCTTCCTGCTATCTCGTAAGAG A G DCPS Ensembl:ENSG00000110063 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs531934504 Functional Loss SNV dbSNP153 33..33 33 - - - 28661 RMVar_ID_28661 Human_SNP_ID_485537005 A-to-I Human chr11 - 126354349 126354349 126354349 CAGGCTGGAGTGCACTGGCGTGATCTTGGCTCACTGCAACCTCTGCCTCCCGGGTTCAAGTGATT CAGGCTGGAGTGCACTGGCGTGATCTTGGCTCGCTGCAACCTCTGCCTCCCGGGTTCAAGTGATT T C GSEC Ensembl:ENSG00000280832 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs866973994 Functional Loss SNV dbSNP153 33..33 33 - - - 28662 RMVar_ID_28662 Human_SNP_ID_485537006 A-to-I Human chr11 - 126354349 126354349 126354349 CAGGCTGGAGTGCACTGGCGTGATCTTGGCTCACTGCAACCTCTGCCTCCCGGGTTCAAGTGATT CAGGCTGGAGTGCACTGGCGTGATCTTGGCTCCCTGCAACCTCTGCCTCCCGGGTTCAAGTGATT T G GSEC Ensembl:ENSG00000280832 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs866973994 Functional Loss SNV dbSNP153 33..33 33 - - - 28663 RMVar_ID_28663 Human_SNP_ID_485685314 A-to-I Human chr11 - 126941396 126941396 126941396 ACTCATCTCTGTATACTTCTAATTGCTTCCCAAGTGATTCTGATTATTAGCAGACTTGCAGCCAC ACTCATCTCTGTATACTTCTAATTGCTTCCCAGGTGATTCTGATTATTAGCAGACTTGCAGCCAC T C KIRREL3 Ensembl:ENSG00000149571 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs962790879 Functional Loss SNV dbSNP153 33..33 33 - - - 28664 RMVar_ID_28664 Human_SNP_ID_485936598 A-to-I Human chr11 - 127941471 127941471 127941471 GGCATATGAAGTGCTGTCGGATGCTAAGAAACAGGACATCTATGACAAATATGGCAAAGAAGGAT GGCATATGAAGTGCTGTCGGATGCTAAGAAACGGGACATCTATGACAAATATGGCAAAGAAGGAT T C AP001000.1 Ensembl:ENSG00000254612 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs571669348 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4152788,Human_RBP_ID_26402165 Human_miRNA_ID_1866718,Human_miRNA_ID_1866998 28665 RMVar_ID_28665 Human_SNP_ID_486303445 A-to-I Human chr11 + 129419880 129419880 129419880 TCGGCTCACTGCAGCCTCCGCCTCCCGGGTTCAAGCGATTCTCATGCCTCGGCCTCCCAAGTAGC TCGGCTCACTGCAGCCTCCGCCTCCCGGGTTCCAGCGATTCTCATGCCTCGGCCTCCCAAGTAGC A C BARX2 Ensembl:ENSG00000043039 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1487143440 Functional Loss SNV dbSNP153 33..33 33 - - - 28666 RMVar_ID_28666 Human_SNP_ID_486418535 A-to-I Human chr11 - 129876801 129876801 129876801 TGTGGTGGGGCCAGTGAAGGGCGTGTTTGACAAGGAGACCTCGCTCAACAAGGCTCGGGAGCACT TGTGGTGGGGCCAGTGAAGGGCGTGTTTGACAGGGAGACCTCGCTCAACAAGGCTCGGGAGCACT T C NFRKB Ensembl:ENSG00000170322 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1019968033 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_227012,Human_RBP_ID_18975167 Human_Splice_Rec_1316774,Human_Splice_Rec_1316775,Human_Splice_Rec_1316822,Human_Splice_Rec_1316823,Human_Splice_Rec_1316874,Human_Splice_Rec_1316875,Human_Splice_Rec_1316924,Human_Splice_Rec_1316925 RMVar_hsa_circ_8236,RMVar_hsa_circ_85437,RMVar_hsa_circ_154015,RMVar_hsa_circ_105574,RMVar_hsa_circ_154016,RMVar_hsa_circ_334159 28667 RMVar_ID_28667 Human_SNP_ID_486425517 A-to-I Human chr11 - 129901336 129901336 129901336 TTTAACTCTTGCTGACATGTTCAGTGTATTTTATTACTTTTAATGCTGTCTTAAAATGAACATTC TTTAACTCTTGCTGACATGTTCAGTGTATTTTGTTACTTTTAATGCTGTCTTAAAATGAACATTC T C PRDM10 Ensembl:ENSG00000170325 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1161917788 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_850534,Human_miRNA_ID_2374110 RMVar_hsa_circ_109588,RMVar_hsa_circ_154020 28668 RMVar_ID_28668 Human_SNP_ID_486445185 A-to-I Human chr11 - 129982899 129982899 129982899 TGGAGTGCAGTGGTGCCATCTCAGCTCACTGCAACTTCTGCCTGTGAGGCACAAGTGATCCTCCC TGGAGTGCAGTGGTGCCATCTCAGCTCACTGCGACTTCTGCCTGTGAGGCACAAGTGATCCTCCC T C PRDM10 Ensembl:ENSG00000170325 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1467299979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17560743 28669 RMVar_ID_28669 Human_SNP_ID_486448988 A-to-I Human chr11 - 129997288 129997288 129997288 TTTTGTAGAGACAGAGTCTTGCCACGTTGCCCAGGCTGGTCTGGAACTCCTGTGGCTCAAGCGAT TTTTGTAGAGACAGAGTCTTGCCACGTTGCCCGGGCTGGTCTGGAACTCCTGTGGCTCAAGCGAT T C PRDM10 Ensembl:ENSG00000170325 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1262055482 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_752400,Human_RBP_ID_11561337 28670 RMVar_ID_28670 Human_SNP_ID_476418348 A-to-I Human chr11 - 90212894 90212894 90212894 TGAGAGGCCAGGCACTGTGGCTCAAGCCCATAATCCAGCACTTTGAGAAGCCTAGGAGGGAGGAT TGAGAGGCCAGGCACTGTGGCTCAAGCCCATATTCCAGCACTTTGAGAAGCCTAGGAGGGAGGAT T A CHORDC1 Ensembl:ENSG00000110172 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs997674363 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5027,RMVar_hsa_circ_351983,RMVar_hsa_circ_48504,RMVar_hsa_circ_152405,RMVar_hsa_circ_78665,RMVar_hsa_circ_367916,RMVar_hsa_circ_68418 28671 RMVar_ID_28671 Human_SNP_ID_476436481 A-to-I Human chr11 + 90282615 90282615 90282615 TCTTAGCTTGTTGGGGACGGTAACCGGGACCCAGTGTCTGCTCCTGTCACCTTCGCCTCCTAATC TCTTAGCTTGTTGGGGACGGTAACCGGGACCCGGTGTCTGCTCCTGTCACCTTCGCCTCCTAATC A G DISC1FP1,TUBAP2 Ensembl:ENSG00000261645,Ensembl:ENSG00000214391 lincRNA,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878893494 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8361185,Human_RBP_ID_27208141 Human_miRNA_ID_1893441 28672 RMVar_ID_28672 Human_SNP_ID_476436485 A-to-I Human chr11 + 90282631 90282631 90282631 ACGGTAACCGGGACCCAGTGTCTGCTCCTGTCACCTTCGCCTCCTAATCCCTAGCCACTATGCGT ACGGTAACCGGGACCCAGTGTCTGCTCCTGTCGCCTTCGCCTCCTAATCCCTAGCCACTATGCGT A G DISC1FP1,TUBAP2 Ensembl:ENSG00000261645,Ensembl:ENSG00000214391 lincRNA,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879104709 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4185329,Human_RBP_ID_8361185,Human_RBP_ID_26407803,Human_RBP_ID_27208141 Human_miRNA_ID_1893441 28673 RMVar_ID_28673 Human_SNP_ID_476436563 A-to-I Human chr11 - 90282825 90282825 90282825 ACAAACACAGCCCGGGGCACATGCTTGCCAGCACCCGTCTCACTGAAGGTGTTGAAGGAGTCATC ACAAACACAGCCCGGGGCACATGCTTGCCAGCGCCCGTCTCACTGAAGGTGTTGAAGGAGTCATC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878992686 Functional Loss SNV dbSNP153 33..33 33 - - - 28674 RMVar_ID_28674 Human_SNP_ID_476436568 A-to-I Human chr11 - 90282837 90282837 90282837 GGTTCCAAGTCTACAAACACAGCCCGGGGCACATGCTTGCCAGCACCCGTCTCACTGAAGGTGTT GGTTCCAAGTCTACAAACACAGCCCGGGGCACGTGCTTGCCAGCACCCGTCTCACTGAAGGTGTT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878985568 Functional Loss SNV dbSNP153 33..33 33 - - - 28675 RMVar_ID_28675 Human_SNP_ID_476436584 A-to-I Human chr11 - 90282872 90282872 90282872 GGTAGGTGCCAGTGCAAACTTCATCAATGACCATGGGTTCCAAGTCTACAAACACAGCCCGGGGC GGTAGGTGCCAGTGCAAACTTCATCAATGACCGTGGGTTCCAAGTCTACAAACACAGCCCGGGGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879245602 Functional Loss SNV dbSNP153 33..33 33 - - - 28676 RMVar_ID_28676 Human_SNP_ID_476436618 A-to-I Human chr11 - 90283005 90283005 90283005 TGGTTAGCCAGCTTGCGAATTCGGTCCAACACAAGGTCAATGATCTCCTTGCCAATGGTGTAGTG TGGTTAGCCAGCTTGCGAATTCGGTCCAACACGAGGTCAATGATCTCCTTGCCAATGGTGTAGTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878865124 Functional Loss SNV dbSNP153 33..33 33 - - - 28677 RMVar_ID_28677 Human_SNP_ID_476436630 A-to-I Human chr11 - 90283032 90283032 90283032 ACCAAGAAGCCCTGAAAACCAGTGCACTGGTTAGCCAGCTTGCGAATTCGGTCCAACACAAGGTC ACCAAGAAGCCCTGAAAACCAGTGCACTGGTTGGCCAGCTTGCGAATTCGGTCCAACACAAGGTC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs979344870 Functional Loss SNV dbSNP153 33..33 33 - - - 28678 RMVar_ID_28678 Human_SNP_ID_476436633 A-to-I Human chr11 - 90283044 90283044 90283044 AAGCTGTGGAAAACCAAGAAGCCCTGAAAACCAGTGCACTGGTTAGCCAGCTTGCGAATTCGGTC AAGCTGTGGAAAACCAAGAAGCCCTGAAAACCGGTGCACTGGTTAGCCAGCTTGCGAATTCGGTC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879176955 Functional Loss SNV dbSNP153 33..33 33 - - - 28679 RMVar_ID_28679 Human_SNP_ID_476436634 A-to-I Human chr11 - 90283044 90283044 90283044 AAGCTGTGGAAAACCAAGAAGCCCTGAAAACCAGTGCACTGGTTAGCCAGCTTGCGAATTCGGTC AAGCTGTGGAAAACCAAGAAGCCCTGAAAACCCGTGCACTGGTTAGCCAGCTTGCGAATTCGGTC T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879176955 Functional Loss SNV dbSNP153 33..33 33 - - - 28680 RMVar_ID_28680 Human_SNP_ID_476436635 A-to-I Human chr11 - 90283048 90283048 90283048 ACCAAAGCTGTGGAAAACCAAGAAGCCCTGAAAACCAGTGCACTGGTTAGCCAGCTTGCGAATTC ACCAAAGCTGTGGAAAACCAAGAAGCCCTGAAGACCAGTGCACTGGTTAGCCAGCTTGCGAATTC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879097595 Functional Loss SNV dbSNP153 33..33 33 - - - 28681 RMVar_ID_28681 Human_SNP_ID_476436636 A-to-I Human chr11 - 90283050 90283050 90283050 CCACCAAAGCTGTGGAAAACCAAGAAGCCCTGAAAACCAGTGCACTGGTTAGCCAGCTTGCGAAT CCACCAAAGCTGTGGAAAACCAAGAAGCCCTGGAAACCAGTGCACTGGTTAGCCAGCTTGCGAAT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1267790143 Functional Loss SNV dbSNP153 33..33 33 - - - 28682 RMVar_ID_28682 Human_SNP_ID_476660767 A-to-I Human chr11 - 91114787 91114787 91114787 AAGAAATTCAGTGGGAGACAAGGTTATTTCATAAAGATGGAGAATATTGGGTTTATGATGAACCA AAGAAATTCAGTGGGAGACAAGGTTATTTCATGAAGATGGAGAATATTGGGTTTATGATGAACCA T C OSBPL9P2 Ensembl:ENSG00000254677 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs983286775 Functional Loss SNV dbSNP153 33..33 33 - - - 28683 RMVar_ID_28683 Human_SNP_ID_476660981 A-to-I Human chr11 - 91115478 91115478 91115478 ATACTGAAGAGAACACAAAACTAGTTTCAGAAAGACCAGTTCCCTGGGTTTCCAAAAATACTGTA ATACTGAAGAGAACACAAAACTAGTTTCAGAAGGACCAGTTCCCTGGGTTTCCAAAAATACTGTA T C OSBPL9P2 Ensembl:ENSG00000254677 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1374333411 Functional Loss SNV dbSNP153 33..33 33 - - - 28684 RMVar_ID_28684 Human_SNP_ID_476660984 A-to-I Human chr11 - 91115493 91115493 91115493 GGACACTACCAAATGATACTGAAGAGAACACAAAACTAGTTTCAGAAAGACCAGTTCCCTGGGTT GGACACTACCAAATGATACTGAAGAGAACACAGAACTAGTTTCAGAAAGACCAGTTCCCTGGGTT T C OSBPL9P2 Ensembl:ENSG00000254677 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1333717953 Functional Loss SNV dbSNP153 33..33 33 - - - 28685 RMVar_ID_28685 Human_SNP_ID_476661130 A-to-I Human chr11 + 91116017 91116017 91116017 ATTAAAGTCTTTTGATGACAAGCTTCAAAACTACAAAGAAGATGAACAGAGAAAGAAAATGGAAA ATTAAAGTCTTTTGATGACAAGCTTCAAAACTGCAAAGAAGATGAACAGAGAAAGAAAATGGAAA A G OSBPL9P3 Ensembl:ENSG00000255070 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1392461697 Functional Loss SNV dbSNP153 33..33 33 - - - 28686 RMVar_ID_28686 Human_SNP_ID_477272852 A-to-I Human chr11 - 93535582 93535582 93535582 AAAGCCCTCCACAGTACCTTTCTTTGGAATGGATTTGGTTCGACTGTCATACTTCTTCAAGGTGA AAAGCCCTCCACAGTACCTTTCTTTGGAATGGGTTTGGTTCGACTGTCATACTTCTTCAAGGTGA T C SMCO4 Ensembl:ENSG00000166002 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs537300637 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23527276 RMVar_hsa_circ_92554,RMVar_hsa_circ_152452 28687 RMVar_ID_28687 Human_SNP_ID_477309426 A-to-I Human chr11 + 93685593 93685593 93685593 AGGTTACTGTGTTTTGACTTTGGCATAAGCTTAGCAGAAGATGGTTTCAGGGCTGACTTGCCTTC AGGTTACTGTGTTTTGACTTTGGCATAAGCTTGGCAGAAGATGGTTTCAGGGCTGACTTGCCTTC A G CEP295 Ensembl:ENSG00000166004 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10765632 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12356,RMVar_hsa_circ_89988,RMVar_hsa_circ_50583,RMVar_hsa_circ_65090,RMVar_hsa_circ_16993,RMVar_hsa_circ_13550,RMVar_hsa_circ_68340,RMVar_hsa_circ_82422,RMVar_hsa_circ_70876,RMVar_hsa_circ_152454,RMVar_hsa_circ_265436,RMVar_hsa_circ_370800,RMVar_hsa_circ_110503,RMVar_hsa_circ_79022,RMVar_hsa_circ_152456,RMVar_hsa_circ_47727,RMVar_hsa_circ_65537,RMVar_hsa_circ_152457,RMVar_hsa_circ_152458,RMVar_hsa_circ_70799,RMVar_hsa_circ_152459,RMVar_hsa_circ_152455,RMVar_hsa_circ_273869,RMVar_hsa_circ_366984,RMVar_hsa_circ_376081,RMVar_hsa_circ_152460,RMVar_hsa_circ_66169,RMVar_hsa_circ_152461 28688 RMVar_ID_28688 Human_SNP_ID_477318790 A-to-I Human chr11 + 93722301 93722301 93722301 TGGGCAACGTGGTAGAACCCTATCTCTACAAAAAAATACAAAAGTTAGCCAGGTGTGGTGGTAAG TGGGCAACGTGGTAGAACCCTATCTCTACAAAGAAATACAAAAGTTAGCCAGGTGTGGTGGTAAG A G CEP295 Ensembl:ENSG00000166004 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs977304211 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_65090,RMVar_hsa_circ_13550,RMVar_hsa_circ_82422,RMVar_hsa_circ_70876,RMVar_hsa_circ_265436,RMVar_hsa_circ_79022,RMVar_hsa_circ_152456,RMVar_hsa_circ_65537,RMVar_hsa_circ_152455,RMVar_hsa_circ_312395,RMVar_hsa_circ_76807,RMVar_hsa_circ_152464,RMVar_hsa_circ_335063,RMVar_hsa_circ_41859,RMVar_hsa_circ_28710,RMVar_hsa_circ_63657,RMVar_hsa_circ_318534,RMVar_hsa_circ_65629,RMVar_hsa_circ_354384,RMVar_hsa_circ_332464,RMVar_hsa_circ_276351,RMVar_hsa_circ_152470,RMVar_hsa_circ_11804,RMVar_hsa_circ_152471 28689 RMVar_ID_28689 Human_SNP_ID_477318792 A-to-I Human chr11 + 93722308 93722307 93722309 CGTGGTAGAACCCTATCTCTACAAAAAAATACAAAAGTTAGCCAGGTGTGGTGGTAAGTGCCTGT CGTGGTAGAACCCTATCTCTACAAAAAAATAC__AAGTTAGCCAGGTGTGGTGGTAAGTGCCTGT CAA C CEP295 Ensembl:ENSG00000166004 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1387510229 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_65090,RMVar_hsa_circ_13550,RMVar_hsa_circ_82422,RMVar_hsa_circ_70876,RMVar_hsa_circ_265436,RMVar_hsa_circ_79022,RMVar_hsa_circ_152456,RMVar_hsa_circ_65537,RMVar_hsa_circ_152455,RMVar_hsa_circ_312395,RMVar_hsa_circ_76807,RMVar_hsa_circ_152464,RMVar_hsa_circ_335063,RMVar_hsa_circ_41859,RMVar_hsa_circ_28710,RMVar_hsa_circ_63657,RMVar_hsa_circ_318534,RMVar_hsa_circ_65629,RMVar_hsa_circ_354384,RMVar_hsa_circ_332464,RMVar_hsa_circ_276351,RMVar_hsa_circ_152470,RMVar_hsa_circ_11804,RMVar_hsa_circ_152471 28690 RMVar_ID_28690 Human_SNP_ID_477321178 A-to-I Human chr11 - 93730326 93730324 93730327 TTCCTCGAATAACAATTTATTGACTTTAAATAATTTTGTCTAATGCTACATATACACAATTAAAA TTCCTCGAATAACAATTTATTGACTTTAAAT___TTTGTCTAATGCTACATATACACAATTAAAA AATT A TAF1D Ensembl:ENSG00000166012 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1419560553 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_406339,Human_RBP_ID_1461316,Human_RBP_ID_1783820,Human_RBP_ID_2291888,Human_RBP_ID_3382805,Human_RBP_ID_8361507,Human_RBP_ID_9364227,Human_RBP_ID_18614592,Human_RBP_ID_24404622,Human_RBP_ID_24462726,Human_RBP_ID_26898936,Human_RBP_ID_27557488 28691 RMVar_ID_28691 Human_SNP_ID_477322371 A-to-I Human chr11 - 93733750 93733750 93733750 TGGAGGCTAAGGCAGGAGAAACACTTGAGCCCAGCGGTTTGAGGCTACAGTGAGATGTGATCCTG TGGAGGCTAAGGCAGGAGAAACACTTGAGCCCGGCGGTTTGAGGCTACAGTGAGATGTGATCCTG T C TAF1D,MIR1304 Ensembl:ENSG00000166012,Ensembl:ENSG00000284458 Protein coding,miRNA intron,exon GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs370314043 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8247400,Human_RBP_ID_10482385,Human_RBP_ID_18510853,Human_RBP_ID_18526299,Human_RBP_ID_19055707,Human_RBP_ID_23113250 Human_miRNA_ID_2517141,Human_miRNA_ID_2554086,Human_miRNA_ID_3135441,Human_miRNA_ID_3135966 RMVar_hsa_circ_18352,RMVar_hsa_circ_328217,RMVar_hsa_circ_335162,RMVar_hsa_circ_10167,RMVar_hsa_circ_13604,RMVar_hsa_circ_12644,RMVar_hsa_circ_45263,RMVar_hsa_circ_152484,RMVar_hsa_circ_100091,RMVar_hsa_circ_370278,RMVar_hsa_circ_152483,RMVar_hsa_circ_361191 28692 RMVar_ID_28692 Human_SNP_ID_477322690 A-to-I Human chr11 - 93734902 93734902 93734902 AAAATTAGCTGGGTACTGGGGCATGTGCCTGTAGTTGGAGTTACTCAGAAAGGGGGGAGGCTGAG AAAATTAGCTGGGTACTGGGGCATGTGCCTGTTGTTGGAGTTACTCAGAAAGGGGGGAGGCTGAG T A TAF1D Ensembl:ENSG00000166012 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1031173562 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_406389,Human_RBP_ID_1461372,Human_RBP_ID_2292010,Human_RBP_ID_6105884,Human_RBP_ID_8361565,Human_RBP_ID_11749875,Human_RBP_ID_18614632 RMVar_hsa_circ_18352,RMVar_hsa_circ_328217,RMVar_hsa_circ_10167,RMVar_hsa_circ_13604,RMVar_hsa_circ_12644,RMVar_hsa_circ_45263,RMVar_hsa_circ_152484,RMVar_hsa_circ_100091,RMVar_hsa_circ_370278,RMVar_hsa_circ_152483,RMVar_hsa_circ_361191,RMVar_hsa_circ_24842,RMVar_hsa_circ_45946 28693 RMVar_ID_28693 Human_SNP_ID_477322697 A-to-I Human chr11 - 93734920 93734920 93734920 CATCTCCACAAAAATTTAAAAATTAGCTGGGTACTGGGGCATGTGCCTGTAGTTGGAGTTACTCA CATCTCCACAAAAATTTAAAAATTAGCTGGGTGCTGGGGCATGTGCCTGTAGTTGGAGTTACTCA T C TAF1D Ensembl:ENSG00000166012 Protein coding intron GSE38233;GSE100210;GSE112787 cultured B-cells;HepG2 cell line;293 Flip-In T-REx cells,empty vector - 24183664,29129909,29967493 RNA-Seq:(High) rs1467733370 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6105884,Human_RBP_ID_11749875,Human_RBP_ID_17803436,Human_RBP_ID_27416976 RMVar_hsa_circ_18352,RMVar_hsa_circ_328217,RMVar_hsa_circ_10167,RMVar_hsa_circ_13604,RMVar_hsa_circ_12644,RMVar_hsa_circ_45263,RMVar_hsa_circ_152484,RMVar_hsa_circ_100091,RMVar_hsa_circ_370278,RMVar_hsa_circ_152483,RMVar_hsa_circ_361191,RMVar_hsa_circ_24842,RMVar_hsa_circ_45946 28694 RMVar_ID_28694 Human_SNP_ID_477322698 A-to-I Human chr11 - 93734920 93734920 93734920 CATCTCCACAAAAATTTAAAAATTAGCTGGGTACTGGGGCATGTGCCTGTAGTTGGAGTTACTCA CATCTCCACAAAAATTTAAAAATTAGCTGGGTCCTGGGGCATGTGCCTGTAGTTGGAGTTACTCA T G TAF1D Ensembl:ENSG00000166012 Protein coding intron GSE38233;GSE100210;GSE112787 cultured B-cells;HepG2 cell line;293 Flip-In T-REx cells,empty vector - 24183664,29129909,29967493 RNA-Seq:(High) rs1467733370 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6105884,Human_RBP_ID_11749875,Human_RBP_ID_17803436,Human_RBP_ID_27416976 RMVar_hsa_circ_18352,RMVar_hsa_circ_328217,RMVar_hsa_circ_10167,RMVar_hsa_circ_13604,RMVar_hsa_circ_12644,RMVar_hsa_circ_45263,RMVar_hsa_circ_152484,RMVar_hsa_circ_100091,RMVar_hsa_circ_370278,RMVar_hsa_circ_152483,RMVar_hsa_circ_361191,RMVar_hsa_circ_24842,RMVar_hsa_circ_45946 28695 RMVar_ID_28695 Human_SNP_ID_477322700 A-to-I Human chr11 - 93734928 93734928 93734928 AAGAAACACATCTCCACAAAAATTTAAAAATTAGCTGGGTACTGGGGCATGTGCCTGTAGTTGGA AAGAAACACATCTCCACAAAAATTTAAAAATTGGCTGGGTACTGGGGCATGTGCCTGTAGTTGGA T C TAF1D Ensembl:ENSG00000166012 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1063080 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6105884,Human_RBP_ID_8062771,Human_RBP_ID_11749875,Human_RBP_ID_17803436,Human_RBP_ID_27416976 RMVar_hsa_circ_18352,RMVar_hsa_circ_328217,RMVar_hsa_circ_10167,RMVar_hsa_circ_13604,RMVar_hsa_circ_12644,RMVar_hsa_circ_45263,RMVar_hsa_circ_152484,RMVar_hsa_circ_100091,RMVar_hsa_circ_370278,RMVar_hsa_circ_152483,RMVar_hsa_circ_361191,RMVar_hsa_circ_24842,RMVar_hsa_circ_45946 28696 RMVar_ID_28696 Human_SNP_ID_477322705 A-to-I Human chr11 - 93734940 93734940 93734940 AGGCAAGAAAGTAAGAAACACATCTCCACAAAAATTTAAAAATTAGCTGGGTACTGGGGCATGTG AGGCAAGAAAGTAAGAAACACATCTCCACAAAGATTTAAAAATTAGCTGGGTACTGGGGCATGTG T C TAF1D Ensembl:ENSG00000166012 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049265813 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6105888,Human_RBP_ID_8062771,Human_RBP_ID_11749875,Human_RBP_ID_17803437,Human_RBP_ID_22894639,Human_RBP_ID_27416976 RMVar_hsa_circ_18352,RMVar_hsa_circ_328217,RMVar_hsa_circ_10167,RMVar_hsa_circ_13604,RMVar_hsa_circ_12644,RMVar_hsa_circ_45263,RMVar_hsa_circ_152484,RMVar_hsa_circ_100091,RMVar_hsa_circ_370278,RMVar_hsa_circ_152483,RMVar_hsa_circ_361191,RMVar_hsa_circ_24842,RMVar_hsa_circ_45946 28697 RMVar_ID_28697 Human_SNP_ID_477322706 A-to-I Human chr11 - 93734940 93734940 93734940 AGGCAAGAAAGTAAGAAACACATCTCCACAAAAATTTAAAAATTAGCTGGGTACTGGGGCATGTG AGGCAAGAAAGTAAGAAACACATCTCCACAAACATTTAAAAATTAGCTGGGTACTGGGGCATGTG T G TAF1D Ensembl:ENSG00000166012 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049265813 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6105888,Human_RBP_ID_8062771,Human_RBP_ID_11749875,Human_RBP_ID_17803437,Human_RBP_ID_22894639,Human_RBP_ID_27416976 RMVar_hsa_circ_18352,RMVar_hsa_circ_328217,RMVar_hsa_circ_10167,RMVar_hsa_circ_13604,RMVar_hsa_circ_12644,RMVar_hsa_circ_45263,RMVar_hsa_circ_152484,RMVar_hsa_circ_100091,RMVar_hsa_circ_370278,RMVar_hsa_circ_152483,RMVar_hsa_circ_361191,RMVar_hsa_circ_24842,RMVar_hsa_circ_45946 28698 RMVar_ID_28698 Human_SNP_ID_477322718 A-to-I Human chr11 - 93735014 93735014 93735014 TGCAATGGGTCAAGCCTGCAATCCCCACACCAAGGTGGGAGTATTGCTTGAAACCAGGAGTTCAA TGCAATGGGTCAAGCCTGCAATCCCCACACCAGGGTGGGAGTATTGCTTGAAACCAGGAGTTCAA T C TAF1D Ensembl:ENSG00000166012 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1210238509 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_226858,Human_RBP_ID_11749889,Human_RBP_ID_23155274,Human_RBP_ID_24909267 Human_Splice_Rec_1287887,Human_Splice_Rec_1287977 RMVar_hsa_circ_18352,RMVar_hsa_circ_328217,RMVar_hsa_circ_10167,RMVar_hsa_circ_13604,RMVar_hsa_circ_12644,RMVar_hsa_circ_45263,RMVar_hsa_circ_152484,RMVar_hsa_circ_100091,RMVar_hsa_circ_370278,RMVar_hsa_circ_152483,RMVar_hsa_circ_361191,RMVar_hsa_circ_24842,RMVar_hsa_circ_45946 28699 RMVar_ID_28699 Human_SNP_ID_477322733 A-to-I Human chr11 - 93735049 93735049 93735049 GTATTGATAGCCATAAAGGTTGGTTCCAGGCCAGGTGCAATGGGTCAAGCCTGCAATCCCCACAC GTATTGATAGCCATAAAGGTTGGTTCCAGGCCCGGTGCAATGGGTCAAGCCTGCAATCCCCACAC T G TAF1D Ensembl:ENSG00000166012 Protein coding intron GSE38233;GSE100210;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 24183664,29129909,30559470 RNA-Seq:(High) rs1010220517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_750066,Human_RBP_ID_808713,Human_RBP_ID_6117459,Human_RBP_ID_17560129,Human_RBP_ID_17803438,Human_RBP_ID_23527478 Human_Splice_Rec_1287887,Human_Splice_Rec_1287977 RMVar_hsa_circ_18352,RMVar_hsa_circ_328217,RMVar_hsa_circ_10167,RMVar_hsa_circ_13604,RMVar_hsa_circ_12644,RMVar_hsa_circ_45263,RMVar_hsa_circ_152484,RMVar_hsa_circ_100091,RMVar_hsa_circ_370278,RMVar_hsa_circ_152483,RMVar_hsa_circ_361191,RMVar_hsa_circ_24842,RMVar_hsa_circ_45946 28700 RMVar_ID_28700 Human_SNP_ID_477322891 A-to-I Human chr11 - 93735426 93735426 93735426 CGCCTGCCTTGGCCTCCCAAAATGCTGGGATTATAGGTGTGAGCCATGGCACCTGGCCTAATACT CGCCTGCCTTGGCCTCCCAAAATGCTGGGATTGTAGGTGTGAGCCATGGCACCTGGCCTAATACT T C TAF1D Ensembl:ENSG00000166012 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs377242290 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9652443,Human_RBP_ID_17560130,Human_RBP_ID_18614634,Human_RBP_ID_27416978 RMVar_hsa_circ_18352,RMVar_hsa_circ_328217,RMVar_hsa_circ_10167,RMVar_hsa_circ_13604,RMVar_hsa_circ_12644,RMVar_hsa_circ_45263,RMVar_hsa_circ_152484,RMVar_hsa_circ_100091,RMVar_hsa_circ_370278,RMVar_hsa_circ_152483,RMVar_hsa_circ_361191,RMVar_hsa_circ_24842,RMVar_hsa_circ_45946 28701 RMVar_ID_28701 Human_SNP_ID_477322901 A-to-I Human chr11 - 93735478 93735478 93735478 TTAGTAGAGACAGGCTTTCACCATGGTCTCGAACTCCTGACCTCAGGCGATCCGCCTGCCTTGGC TTAGTAGAGACAGGCTTTCACCATGGTCTCGATCTCCTGACCTCAGGCGATCCGCCTGCCTTGGC T A TAF1D Ensembl:ENSG00000166012 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs749850424 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_406393,Human_RBP_ID_8361568,Human_RBP_ID_11749918,Human_RBP_ID_17560131,Human_RBP_ID_27416979 RMVar_hsa_circ_18352,RMVar_hsa_circ_328217,RMVar_hsa_circ_10167,RMVar_hsa_circ_13604,RMVar_hsa_circ_12644,RMVar_hsa_circ_45263,RMVar_hsa_circ_152484,RMVar_hsa_circ_100091,RMVar_hsa_circ_370278,RMVar_hsa_circ_152483,RMVar_hsa_circ_361191,RMVar_hsa_circ_24842,RMVar_hsa_circ_45946 28702 RMVar_ID_28702 Human_SNP_ID_477322931 A-to-I Human chr11 - 93735559 93735559 93735559 GGTTCAAGCGATTCTGCCTCAGCCTCCTTAGTAGCTGGGATTACAGGCGTTAGCCAGCACACCCA GGTTCAAGCGATTCTGCCTCAGCCTCCTTAGTCGCTGGGATTACAGGCGTTAGCCAGCACACCCA T G TAF1D Ensembl:ENSG00000166012 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs560521048 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1461377,Human_RBP_ID_1783877,Human_RBP_ID_8361569,Human_RBP_ID_18614635,Human_RBP_ID_22894646 RMVar_hsa_circ_18352,RMVar_hsa_circ_328217,RMVar_hsa_circ_10167,RMVar_hsa_circ_13604,RMVar_hsa_circ_12644,RMVar_hsa_circ_45263,RMVar_hsa_circ_152484,RMVar_hsa_circ_100091,RMVar_hsa_circ_370278,RMVar_hsa_circ_152483,RMVar_hsa_circ_361191,RMVar_hsa_circ_24842,RMVar_hsa_circ_45946 28703 RMVar_ID_28703 Human_SNP_ID_477322934 A-to-I Human chr11 - 93735571 93735571 93735571 CTCCATCTCCCGGGTTCAAGCGATTCTGCCTCAGCCTCCTTAGTAGCTGGGATTACAGGCGTTAG CTCCATCTCCCGGGTTCAAGCGATTCTGCCTCGGCCTCCTTAGTAGCTGGGATTACAGGCGTTAG T C TAF1D Ensembl:ENSG00000166012 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1340483072 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1461377,Human_RBP_ID_1783877,Human_RBP_ID_8361569,Human_RBP_ID_18614635,Human_RBP_ID_22894646 RMVar_hsa_circ_18352,RMVar_hsa_circ_328217,RMVar_hsa_circ_10167,RMVar_hsa_circ_13604,RMVar_hsa_circ_12644,RMVar_hsa_circ_45263,RMVar_hsa_circ_152484,RMVar_hsa_circ_100091,RMVar_hsa_circ_370278,RMVar_hsa_circ_152483,RMVar_hsa_circ_361191,RMVar_hsa_circ_24842,RMVar_hsa_circ_45946 28704 RMVar_ID_28704 Human_SNP_ID_477322950 A-to-I Human chr11 - 93735630 93735630 93735630 GAGTCTCGATCTGTCACCCAGGCTGTAGTGCAATGGCCGCAGTCTTGGCTTACTGCAACCTCCAT GAGTCTCGATCTGTCACCCAGGCTGTAGTGCAGTGGCCGCAGTCTTGGCTTACTGCAACCTCCAT T C TAF1D Ensembl:ENSG00000166012 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs887873551 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_807620,Human_RBP_ID_11749926,Human_RBP_ID_26898989 RMVar_hsa_circ_18352,RMVar_hsa_circ_328217,RMVar_hsa_circ_10167,RMVar_hsa_circ_13604,RMVar_hsa_circ_12644,RMVar_hsa_circ_45263,RMVar_hsa_circ_152484,RMVar_hsa_circ_100091,RMVar_hsa_circ_370278,RMVar_hsa_circ_152483,RMVar_hsa_circ_361191,RMVar_hsa_circ_24842,RMVar_hsa_circ_45946 28705 RMVar_ID_28705 Human_SNP_ID_477322962 A-to-I Human chr11 - 93735663 93735660 93735664 TTAGAGTATCTTTAATACTATTTTTTTTAGACAGAGTCTCGATCTGTCACCCAGGCTGTAGTGCA TTAGAGTATCTTTAATACTATTTTTTTTAGA____GTCTCGATCTGTCACCCAGGCTGTAGTGCA CTCTG C TAF1D Ensembl:ENSG00000166012 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1187155267 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_8361570,Human_RBP_ID_11749926,Human_RBP_ID_24462770 RMVar_hsa_circ_18352,RMVar_hsa_circ_328217,RMVar_hsa_circ_10167,RMVar_hsa_circ_13604,RMVar_hsa_circ_12644,RMVar_hsa_circ_45263,RMVar_hsa_circ_152484,RMVar_hsa_circ_100091,RMVar_hsa_circ_370278,RMVar_hsa_circ_152483,RMVar_hsa_circ_361191,RMVar_hsa_circ_24842,RMVar_hsa_circ_45946 28706 RMVar_ID_28706 Human_SNP_ID_477325396 A-to-I Human chr11 + 93743070 93743070 93743070 GCCCAGGCTGGAGTGCAGTGTGGCCCGATCTCAGCTCACTGCAACCCCCACCTCCCGGGCTCAAG GCCCAGGCTGGAGTGCAGTGTGGCCCGATCTCGGCTCACTGCAACCCCCACCTCCCGGGCTCAAG A G AP001273.2,C11orf54 Ensembl:ENSG00000284057,Ensembl:ENSG00000182919 Protein coding,Protein coding intron,intron GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490829,GSM3490830,GSM3490831 HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,EC109 cell line - 29129909,29796672,31158229,31158229,32596459 RNA-Seq:(High) rs941202424 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8361612,Human_RBP_ID_24913457 28707 RMVar_ID_28707 Human_SNP_ID_477329703 A-to-I Human chr11 + 93759779 93759777 93759780 AGAATTTTCTTCCTGCCCCTTGAACTCTGATGAAGAAGTGAATAAATGGTTGCATTTTTATGAAA AGAATTTTCTTCCTGCCCCTTGAACTCTGAT___GAAGTGAATAAATGGTTGCATTTTTATGAAA TGAA T AP001273.2,C11orf54 Ensembl:ENSG00000284057,Ensembl:ENSG00000182919 Protein coding,Protein coding CDS,CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1281819921 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_11750408,Human_RBP_ID_22435601,Human_RBP_ID_23527568 Human_Splice_Rec_1288046,Human_Splice_Rec_1288047,Human_Splice_Rec_1288060,Human_Splice_Rec_1288061,Human_Splice_Rec_1288074,Human_Splice_Rec_1288075,Human_Splice_Rec_1288092,Human_Splice_Rec_1288093,Human_Splice_Rec_1288120,Human_Splice_Rec_1288121,Human_Splice_Rec_1288136,Human_Splice_Rec_1288137,Human_Splice_Rec_1288150,Human_Splice_Rec_1288170,Human_Splice_Rec_1288202,Human_Splice_Rec_1288203,Human_Splice_Rec_1288216,Human_Splice_Rec_1288217 RMVar_hsa_circ_152492,RMVar_hsa_circ_280233,RMVar_hsa_circ_58230,RMVar_hsa_circ_152488,RMVar_hsa_circ_152489,RMVar_hsa_circ_152491,RMVar_hsa_circ_301552,RMVar_hsa_circ_308285,RMVar_hsa_circ_152496,RMVar_hsa_circ_152494,RMVar_hsa_circ_152495,RMVar_hsa_circ_275159,RMVar_hsa_circ_284791 28708 RMVar_ID_28708 Human_SNP_ID_477331597 A-to-I Human chr11 + 93767809 93767809 93767809 TTACCCAGGCTAGAGTGCAATGGCATGATCTCAGCTCACTGCAACCTCTGCCTCCCAGGCTCAAA TTACCCAGGCTAGAGTGCAATGGCATGATCTCCGCTCACTGCAACCTCTGCCTCCCAGGCTCAAA A C AP001273.2 Ensembl:ENSG00000284057 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251571484 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58230 28709 RMVar_ID_28709 Human_SNP_ID_477336501 A-to-I Human chr11 + 93786597 93786597 93786597 CAAAACGATTCTCCCACTTCAGCTTCCCTAGTATGTGGGACTGTAGGCGTGCGGCACCATGCCTG CAAAACGATTCTCCCACTTCAGCTTCCCTAGTGTGTGGGACTGTAGGCGTGCGGCACCATGCCTG A G AP001273.2,MED17 Ensembl:ENSG00000284057,Ensembl:ENSG00000042429 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs755314811 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11750476 RMVar_hsa_circ_58230 28710 RMVar_ID_28710 Human_SNP_ID_477336658 A-to-I Human chr11 + 93787158 93787158 93787158 CACTGGGGCCGGGCGCAGTGGCTCACGTCTGTAATCCCAGCACTTTCGGAGGCCGGGGCAGGCAG CACTGGGGCCGGGCGCAGTGGCTCACGTCTGTGATCCCAGCACTTTCGGAGGCCGGGGCAGGCAG A G AP001273.2,MED17 Ensembl:ENSG00000284057,Ensembl:ENSG00000042429 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs751743462 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58230 28711 RMVar_ID_28711 Human_SNP_ID_477336659 A-to-I Human chr11 + 93787158 93787158 93787158 CACTGGGGCCGGGCGCAGTGGCTCACGTCTGTAATCCCAGCACTTTCGGAGGCCGGGGCAGGCAG CACTGGGGCCGGGCGCAGTGGCTCACGTCTGTTATCCCAGCACTTTCGGAGGCCGGGGCAGGCAG A T AP001273.2,MED17 Ensembl:ENSG00000284057,Ensembl:ENSG00000042429 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs751743462 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58230 28712 RMVar_ID_28712 Human_SNP_ID_477337857 A-to-I Human chr11 + 93791443 93791443 93791443 AAAACTGAACATGGCGGGGTGCAGTGGCTCACACCTGTAATCCTAGCACTTTGGGAGGCTGAGGT AAAACTGAACATGGCGGGGTGCAGTGGCTCACGCCTGTAATCCTAGCACTTTGGGAGGCTGAGGT A G AP001273.2,MED17 Ensembl:ENSG00000284057,Ensembl:ENSG00000042429 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1437983118 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58230,RMVar_hsa_circ_17392,RMVar_hsa_circ_152500,RMVar_hsa_circ_290623,RMVar_hsa_circ_298137,RMVar_hsa_circ_329494,RMVar_hsa_circ_341892,RMVar_hsa_circ_279685,RMVar_hsa_circ_152501,RMVar_hsa_circ_337344,RMVar_hsa_circ_152498,RMVar_hsa_circ_152499,RMVar_hsa_circ_365230,RMVar_hsa_circ_152497,RMVar_hsa_circ_340298,RMVar_hsa_circ_281649,RMVar_hsa_circ_328573,RMVar_hsa_circ_281083,RMVar_hsa_circ_152504,RMVar_hsa_circ_13509,RMVar_hsa_circ_152505,RMVar_hsa_circ_152503 28713 RMVar_ID_28713 Human_SNP_ID_477341893 A-to-I Human chr11 + 93806040 93806040 93806040 AGTTTTGCTCTGTCGCCAGATCGGAGTGCAGTAGTGTGATCTTGGCTCACTGCAACCTCTGCCTC AGTTTTGCTCTGTCGCCAGATCGGAGTGCAGTGGTGTGATCTTGGCTCACTGCAACCTCTGCCTC A G AP001273.2,MED17 Ensembl:ENSG00000284057,Ensembl:ENSG00000042429 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs529130025 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23527617 RMVar_hsa_circ_4932,RMVar_hsa_circ_365230,RMVar_hsa_circ_152497,RMVar_hsa_circ_13509,RMVar_hsa_circ_296689,RMVar_hsa_circ_152508,RMVar_hsa_circ_295657,RMVar_hsa_circ_152511,RMVar_hsa_circ_39908 28714 RMVar_ID_28714 Human_SNP_ID_477341906 A-to-I Human chr11 + 93806118 93806118 93806118 ATTCTGCCTCAGCCTCCCAAATAGCTGGGACTACAGATGTGTGCCACCACGCCCACCTAATTTTT ATTCTGCCTCAGCCTCCCAAATAGCTGGGACTGCAGATGTGTGCCACCACGCCCACCTAATTTTT A G AP001273.2,MED17 Ensembl:ENSG00000284057,Ensembl:ENSG00000042429 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1245971304 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4932,RMVar_hsa_circ_365230,RMVar_hsa_circ_152497,RMVar_hsa_circ_13509,RMVar_hsa_circ_296689,RMVar_hsa_circ_152508,RMVar_hsa_circ_295657,RMVar_hsa_circ_152511,RMVar_hsa_circ_39908 28715 RMVar_ID_28715 Human_SNP_ID_477500860 A-to-I Human chr11 - 94417114 94417114 94417114 AGATTAGCTGGGCATGGTGGTGTGTGCCTGTAATCTTAGCTACTCAGGAGGCTGAGGCAGGAGAA AGATTAGCTGGGCATGGTGGTGTGTGCCTGTAGTCTTAGCTACTCAGGAGGCTGAGGCAGGAGAA T C MRE11 Ensembl:ENSG00000020922 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1411957762 Functional Loss SNV dbSNP153 33..33 33 - - - 28716 RMVar_ID_28716 Human_SNP_ID_477500861 A-to-I Human chr11 - 94417115 94417115 94417115 AAGATTAGCTGGGCATGGTGGTGTGTGCCTGTAATCTTAGCTACTCAGGAGGCTGAGGCAGGAGA AAGATTAGCTGGGCATGGTGGTGTGTGCCTGTGATCTTAGCTACTCAGGAGGCTGAGGCAGGAGA T C MRE11 Ensembl:ENSG00000020922 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1391216185 Functional Loss SNV dbSNP153 33..33 33 - - - 28717 RMVar_ID_28717 Human_SNP_ID_477500869 A-to-I Human chr11 - 94417133 94417133 94417133 TCTCTACTAAAAATACAAAAGATTAGCTGGGCATGGTGGTGTGTGCCTGTAATCTTAGCTACTCA TCTCTACTAAAAATACAAAAGATTAGCTGGGCGTGGTGGTGTGTGCCTGTAATCTTAGCTACTCA T C MRE11 Ensembl:ENSG00000020922 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs778842426 Functional Loss SNV dbSNP153 33..33 33 - - - 28718 RMVar_ID_28718 Human_SNP_ID_477500870 A-to-I Human chr11 - 94417133 94417133 94417133 TCTCTACTAAAAATACAAAAGATTAGCTGGGCATGGTGGTGTGTGCCTGTAATCTTAGCTACTCA TCTCTACTAAAAATACAAAAGATTAGCTGGGCCTGGTGGTGTGTGCCTGTAATCTTAGCTACTCA T G MRE11 Ensembl:ENSG00000020922 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs778842426 Functional Loss SNV dbSNP153 33..33 33 - - - 28719 RMVar_ID_28719 Human_SNP_ID_477500899 A-to-I Human chr11 - 94417249 94417249 94417249 CAATGGGCTGGGTGCAGTGGCTCATGCCTTTAATCCCAGCACTTTGGGAGGCCGAGGAGGGGGTT CAATGGGCTGGGTGCAGTGGCTCATGCCTTTAGTCCCAGCACTTTGGGAGGCCGAGGAGGGGGTT T C MRE11 Ensembl:ENSG00000020922 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1133564 Functional Loss SNV dbSNP153 33..33 33 - - - 28720 RMVar_ID_28720 Human_SNP_ID_477821298 A-to-I Human chr11 - 95770397 95770397 95770397 AATATTTATGTACAATGTAATTTGTAAATTTAAAGCAAATCTGAAAAAAATTAAATGATCTTTTT AATATTTATGTACAATGTAATTTGTAAATTTATAGCAAATCTGAAAAAAATTAAATGATCTTTTT T A FAM76B Ensembl:ENSG00000077458 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs867015771 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1461726,Human_RBP_ID_1784321 RMVar_hsa_circ_105762,RMVar_hsa_circ_152576 28721 RMVar_ID_28721 Human_SNP_ID_477845759 A-to-I Human chr11 - 95859550 95859550 95859550 TGCATTTAAAGAATGTCGGTAGATAAGAACATAGGAAAAGTCTACAATACCAATTTTTCCCCACC TGCATTTAAAGAATGTCGGTAGATAAGAACATGGGAAAAGTCTACAATACCAATTTTTCCCCACC T C MTMR2 Ensembl:ENSG00000087053 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355872536 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_152589,RMVar_hsa_circ_92720,RMVar_hsa_circ_90492,RMVar_hsa_circ_266630,RMVar_hsa_circ_49882,RMVar_hsa_circ_53657,RMVar_hsa_circ_101748,RMVar_hsa_circ_84825,RMVar_hsa_circ_152598,RMVar_hsa_circ_152599,RMVar_hsa_circ_152597,RMVar_hsa_circ_324655,RMVar_hsa_circ_363270,RMVar_hsa_circ_54072,RMVar_hsa_circ_33640,RMVar_hsa_circ_152601,RMVar_hsa_circ_50933,RMVar_hsa_circ_21439 28722 RMVar_ID_28722 Human_SNP_ID_477936176 A-to-I Human chr11 - 96233548 96233548 96233548 TAAAAATTAGCTGGATGTGGTGGTGTACACCTATTGTCCTAGCTACTAAGGTGGCTGAGGCAGGA TAAAAATTAGCTGGATGTGGTGGTGTACACCTGTTGTCCTAGCTACTAAGGTGGCTGAGGCAGGA T C MAML2 Ensembl:ENSG00000184384 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1294279690 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101444,RMVar_hsa_circ_152610 28723 RMVar_ID_28723 Human_SNP_ID_222653543 A-to-I Human chr5 - 15451702 15451702 15451702 GATGGAGCTGCTGATTCACACTGAGTACTTGCACTCTGGGGGTGTGATGATCTTGATCTTCATGG GATGGAGCTGCTGATTCACACTGAGTACTTGCTCTCTGGGGGTGTGATGATCTTGATCTTCATGG T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1178287126 Functional Loss SNV dbSNP153 33..33 33 - - - 28724 RMVar_ID_28724 Human_SNP_ID_222895210 A-to-I Human chr5 - 16474667 16474663 16474667 AAATTTCAAACAAGAAAAAAAAAAAAAAAAGGAAAAGAAAAAAATTGAACTGTAAGCTTTAATGA AAATTTCAAACAAGAAAAAAAAAAAAAAAAGG____GAAAAAAATTGAACTGTAAGCTTTAATGA CTTTT C RETREG1 Ensembl:ENSG00000154153 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1160450515 Functional Loss DEL dbSNP153 33..36 33 - - - Human_Splice_Rec_636829 28725 RMVar_ID_28725 Human_SNP_ID_222925928 A-to-I Human chr5 - 16607552 16607552 16607552 TGGAGTGCAGTGGTGTGATCTTGGCTCACTGCAGTCTCCGCCTCCTGGGTTCAAGCGATTCTCCT TGGAGTGCAGTGGTGTGATCTTGGCTCACTGCGGTCTCCGCCTCCTGGGTTCAAGCGATTCTCCT T C RETREG1 Ensembl:ENSG00000154153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs892218343 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_167436 28726 RMVar_ID_28726 Human_SNP_ID_222941798 A-to-I Human chr5 - 16662595 16662595 16662595 AGTTTCAGCCAGGCATGCTGGCTCACGCCTGTAATCCCAGCATGTTGGAAGGCCGAGGCAAGAGG AGTTTCAGCCAGGCATGCTGGCTCACGCCTGTCATCCCAGCATGTTGGAAGGCCGAGGCAAGAGG T G MYO10 Ensembl:ENSG00000145555 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1036257477 Functional Loss SNV dbSNP153 33..33 33 - - - 28727 RMVar_ID_28727 Human_SNP_ID_222942170 A-to-I Human chr5 - 16663591 16663591 16663591 AGCAGTCCTCCACCTCAGCCTCCCAAAGTGCTAGGATGACAGGTGTGAGCCACTGTGCCCCACCA AGCAGTCCTCCACCTCAGCCTCCCAAAGTGCTGGGATGACAGGTGTGAGCCACTGTGCCCCACCA T C MYO10 Ensembl:ENSG00000145555 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1134506 Functional Loss SNV dbSNP153 33..33 33 - - - 28728 RMVar_ID_28728 Human_SNP_ID_222942598 A-to-I Human chr5 - 16665037 16665037 16665037 CACCACGCCTGGCTAGGTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGG CACCACGCCTGGCTAGGTTTTGTATTTTTAGTGGAGATGGGGTTTCACCATGTTGGCCAGGCTGG T C MYO10 Ensembl:ENSG00000145555 Protein coding 3'UTR GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs1489002364 Functional Loss SNV dbSNP153 33..33 33 - - - 28729 RMVar_ID_28729 Human_SNP_ID_222952157 A-to-I Human chr5 - 16698188 16698188 16698188 AGGCTAATTTTTTATAGAGATGGAATCTCACTATGTTGCCCAGGCTGGTCTCCAACTCTTGGCCT AGGCTAATTTTTTATAGAGATGGAATCTCACTGTGTTGCCCAGGCTGGTCTCCAACTCTTGGCCT T C MYO10 Ensembl:ENSG00000145555 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1169564943 Functional Loss SNV dbSNP153 33..33 33 - - - 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_230503,RMVar_hsa_circ_230505,RMVar_hsa_circ_230506,RMVar_hsa_circ_230504,RMVar_hsa_circ_78639,RMVar_hsa_circ_230509,RMVar_hsa_circ_11821,RMVar_hsa_circ_74659 28730 RMVar_ID_28730 Human_SNP_ID_222952172 A-to-I Human chr5 - 16698247 16698247 16698247 GCCATCTTCCTGCCGCAGCCTTCATAGGAGCTAGGACTGCAGGCGCACACCATCATGCCAGGCTA GCCATCTTCCTGCCGCAGCCTTCATAGGAGCTGGGACTGCAGGCGCACACCATCATGCCAGGCTA T C MYO10 Ensembl:ENSG00000145555 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1438821247 Functional Loss SNV dbSNP153 33..33 33 - - - 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_230503,RMVar_hsa_circ_230505,RMVar_hsa_circ_230506,RMVar_hsa_circ_230504,RMVar_hsa_circ_78639,RMVar_hsa_circ_230509,RMVar_hsa_circ_11821,RMVar_hsa_circ_74659 28731 RMVar_ID_28731 Human_SNP_ID_222958808 A-to-I Human chr5 - 16720631 16720631 16720631 ACACGGTGAAATCCCGTCTTTACTAAAAATACAAAAAATTAGCCGGGTGTGGTGGCACGTGCCTA ACACGGTGAAATCCCGTCTTTACTAAAAATACGAAAAATTAGCCGGGTGTGGTGGCACGTGCCTA T C MYO10 Ensembl:ENSG00000145555 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1430220405 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_16909,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_78236,RMVar_hsa_circ_19541,RMVar_hsa_circ_44006,RMVar_hsa_circ_322544,RMVar_hsa_circ_99032,RMVar_hsa_circ_230511,RMVar_hsa_circ_230513,RMVar_hsa_circ_230512,RMVar_hsa_circ_100350,RMVar_hsa_circ_230515 28732 RMVar_ID_28732 Human_SNP_ID_222964473 A-to-I Human chr5 - 16743386 16743386 16743386 CACTCACCTCGGCCTCCCAAAGTGCTGGGATTACAGACGTAAGCCACCGTGTCCAGCTGAGAATG CACTCACCTCGGCCTCCCAAAGTGCTGGGATTGCAGACGTAAGCCACCGTGTCCAGCTGAGAATG T C MYO10 Ensembl:ENSG00000145555 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1004255141 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_16909,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_78236,RMVar_hsa_circ_19541,RMVar_hsa_circ_44006,RMVar_hsa_circ_322544,RMVar_hsa_circ_99032,RMVar_hsa_circ_230511,RMVar_hsa_circ_230513,RMVar_hsa_circ_230512,RMVar_hsa_circ_100350,RMVar_hsa_circ_230515 28733 RMVar_ID_28733 Human_SNP_ID_222965542 A-to-I Human chr5 - 16747755 16747755 16747755 GCCACCCCGCACGGCTAATTTTTTGTATTTTTAGTAGAGACGGGGGTTTCTCTGTGTTAGCCAGA GCCACCCCGCACGGCTAATTTTTTGTATTTTTGGTAGAGACGGGGGTTTCTCTGTGTTAGCCAGA T C MYO10 Ensembl:ENSG00000145555 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs539040024 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_16909,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_78236,RMVar_hsa_circ_19541,RMVar_hsa_circ_44006,RMVar_hsa_circ_322544,RMVar_hsa_circ_99032,RMVar_hsa_circ_230511,RMVar_hsa_circ_230513,RMVar_hsa_circ_230512,RMVar_hsa_circ_100350,RMVar_hsa_circ_230515 28734 RMVar_ID_28734 Human_SNP_ID_222984700 A-to-I Human chr5 - 16816710 16816710 16816710 CCTGGCCAACATGGTGAATCCCCGTCTCTACTAAAAATACAAAAATTAGCTGGGCGTGGTGGCGT CCTGGCCAACATGGTGAATCCCCGTCTCTACTGAAAATACAAAAATTAGCTGGGCGTGGTGGCGT T C MYO10 Ensembl:ENSG00000145555 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs576693187 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 28735 RMVar_ID_28735 Human_SNP_ID_222995460 A-to-I Human chr5 - 16854994 16854994 16854994 GAGTCTCACTGTTGTCGTCTGGGCTGAGTGCAATGGCGCAATCTCGGCTCACTGCAACCTCCGCC GAGTCTCACTGTTGTCGTCTGGGCTGAGTGCAGTGGCGCAATCTCGGCTCACTGCAACCTCCGCC T C MYO10 Ensembl:ENSG00000145555 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1014703759 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15371466 RMVar_hsa_circ_119010,RMVar_hsa_circ_230538,RMVar_hsa_circ_328441,RMVar_hsa_circ_230542,RMVar_hsa_circ_338452 28736 RMVar_ID_28736 Human_SNP_ID_223077066 A-to-I Human chr5 - 17141766 17141766 17141766 ATAGTGAAACCCCATCTCTACTAAAAATACAAAAAATTATCCAGATGTGGTGGTGTATGACTTAC ATAGTGAAACCCCATCTCTACTAAAAATACAATAAATTATCCAGATGTGGTGGTGTATGACTTAC T A BASP1-AS1 Ensembl:ENSG00000215196 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1231085402 Functional Loss SNV dbSNP153 33..33 33 - - - 28737 RMVar_ID_28737 Human_SNP_ID_223081922 A-to-I Human chr5 - 17160777 17160777 17160777 GCCCAGAAGCTCAAGGCCAGCCTAGGCAACATAGTGAGATCCTATCTCTACAAAAAATGAAATTA GCCCAGAAGCTCAAGGCCAGCCTAGGCAACATCGTGAGATCCTATCTCTACAAAAAATGAAATTA T G BASP1-AS1 Ensembl:ENSG00000215196 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1409791811 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_230546,RMVar_hsa_circ_230545 28738 RMVar_ID_28738 Human_SNP_ID_223084158 A-to-I Human chr5 - 17170178 17170178 17170178 GGCATTCACCACCATGCCCAGCTAATTTCTGTATTTTCAGTAGAGACGGGGTTTCACTATGTTGG GGCATTCACCACCATGCCCAGCTAATTTCTGTGTTTTCAGTAGAGACGGGGTTTCACTATGTTGG T C BASP1-AS1 Ensembl:ENSG00000215196 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1000555336 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8269523 RMVar_hsa_circ_230546 28739 RMVar_ID_28739 Human_SNP_ID_223084998 A-to-I Human chr5 - 17173580 17173580 17173580 ACAACCATTAAGATATAGAGCAGGTGACTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGT ACAACCATTAAGATATAGAGCAGGTGACTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGT T C BASP1-AS1 Ensembl:ENSG00000215196 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs902064986 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_230546 28740 RMVar_ID_28740 Human_SNP_ID_223085111 A-to-I Human chr5 - 17174166 17174166 17174166 CCTCGGCCTCCCAAAGTGCTAGGATTACAGGCATGAGCCACCATGCCTGGGCCAACAGCTCTCTT CCTCGGCCTCCCAAAGTGCTAGGATTACAGGCGTGAGCCACCATGCCTGGGCCAACAGCTCTCTT T C BASP1-AS1 Ensembl:ENSG00000215196 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560527282 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_230546 28741 RMVar_ID_28741 Human_SNP_ID_223085112 A-to-I Human chr5 - 17174166 17174166 17174166 CCTCGGCCTCCCAAAGTGCTAGGATTACAGGCATGAGCCACCATGCCTGGGCCAACAGCTCTCTT CCTCGGCCTCCCAAAGTGCTAGGATTACAGGCCTGAGCCACCATGCCTGGGCCAACAGCTCTCTT T G BASP1-AS1 Ensembl:ENSG00000215196 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560527282 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_230546 28742 RMVar_ID_28742 Human_SNP_ID_223089673 A-to-I Human chr5 - 17193317 17193317 17193317 GAGCTGAGGCGGGCGGATCACCTGAGGTCAGGAGTTCGAGACCAGCCTGGTCAACTTGGTAAAAC GAGCTGAGGCGGGCGGATCACCTGAGGTCAGGGGTTCGAGACCAGCCTGGTCAACTTGGTAAAAC T C BASP1-AS1 Ensembl:ENSG00000215196 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1392381252 Functional Loss SNV dbSNP153 33..33 33 - - - 28743 RMVar_ID_28743 Human_SNP_ID_223092138 A-to-I Human chr5 - 17203379 17203379 17203379 GCTCTGCCGCCAGGCTGGACTGAAGTGGCGCAATCTCGGCTCACTGAAACCTCTGCCTCCTGGGT GCTCTGCCGCCAGGCTGGACTGAAGTGGCGCAGTCTCGGCTCACTGAAACCTCTGCCTCCTGGGT T C BASP1-AS1 Ensembl:ENSG00000215196 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1488117883 Functional Loss SNV dbSNP153 33..33 33 - - - 28744 RMVar_ID_28744 Human_SNP_ID_223100589 A-to-I Human chr5 + 17237808 17237808 17237808 AATTTTTGAATTTTTAGTAGAGACAGTGTTTCACCATGTTGGCCAGGCTTGTCTTGAATTCCTCA AATTTTTGAATTTTTAGTAGAGACAGTGTTTCGCCATGTTGGCCAGGCTTGTCTTGAATTCCTCA A G BASP1 Ensembl:ENSG00000176788 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1242452787 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15382321 28745 RMVar_ID_28745 Human_SNP_ID_223100601 A-to-I Human chr5 + 17237854 17237854 17237854 GCTTGTCTTGAATTCCTCACCTCAAGTGATCCACCCACGTCGGCCTCCCAAAGTGCTGGGATTAC GCTTGTCTTGAATTCCTCACCTCAAGTGATCCCCCCACGTCGGCCTCCCAAAGTGCTGGGATTAC A C BASP1 Ensembl:ENSG00000176788 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1373076087 Functional Loss SNV dbSNP153 33..33 33 - - - 28746 RMVar_ID_28746 Human_SNP_ID_223101186 A-to-I Human chr5 + 17240375 17240375 17240375 TGGCCAACATGGTGAAATCCTGTCTCTACTGAAAAATACAAAAATTAGCTGGGCGTGGTGGCGGG TGGCCAACATGGTGAAATCCTGTCTCTACTGAGAAATACAAAAATTAGCTGGGCGTGGTGGCGGG A G BASP1 Ensembl:ENSG00000176788 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1459958229 Functional Loss SNV dbSNP153 33..33 33 - - - 28747 RMVar_ID_28747 Human_SNP_ID_223101188 A-to-I Human chr5 + 17240389 17240389 17240389 AAATCCTGTCTCTACTGAAAAATACAAAAATTAGCTGGGCGTGGTGGCGGGCACCTGTGATTGCA AAATCCTGTCTCTACTGAAAAATACAAAAATTTGCTGGGCGTGGTGGCGGGCACCTGTGATTGCA A T BASP1 Ensembl:ENSG00000176788 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs912555273 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15382405 28748 RMVar_ID_28748 Human_SNP_ID_223102235 A-to-I Human chr5 + 17244871 17244871 17244871 GCGCCACCATGCCCAGCTAATTTTGTAGTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGC GCGCCACCATGCCCAGCTAATTTTGTAGTTTTGGTAGAGATGGGGTTTCACCATGTTGGCCAGGC A G BASP1 Ensembl:ENSG00000176788 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1320683645 Functional Loss SNV dbSNP153 33..33 33 - - - 28749 RMVar_ID_28749 Human_SNP_ID_223102322 A-to-I Human chr5 + 17245265 17245265 17245265 TGGAGGTTGCCGTGAGCTGAGCTCACACCATTACACTCTAGCCTGGGCAACAGAGTGAAAGTGAG TGGAGGTTGCCGTGAGCTGAGCTCACACCATTGCACTCTAGCCTGGGCAACAGAGTGAAAGTGAG A G BASP1 Ensembl:ENSG00000176788 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1335172690 Functional Loss SNV dbSNP153 33..33 33 - - - 28750 RMVar_ID_28750 Human_SNP_ID_223470273 A-to-I Human chr5 - 18736841 18736841 18736841 GTCTCTACCAAAAATACAAAAATTAGCCGGACATGTTGACTCGCTCCTGTAATCCCAGCTACTTA GTCTCTACCAAAAATACAAAAATTAGCCGGACGTGTTGACTCGCTCCTGTAATCCCAGCTACTTA T C LINC02100 Ensembl:ENSG00000248693 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1445880566 Functional Loss SNV dbSNP153 33..33 33 - - - 28751 RMVar_ID_28751 Human_SNP_ID_223708198 A-to-I Human chr5 - 19696666 19696666 19696666 TTTTTGGCTGGGTGCGGTGGCTCACGCTTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGAGGA TTTTTGGCTGGGTGCGGTGGCTCACGCTTGTAGTCCCAGCACTTTGGGAGGCCGAGGCGGGAGGA T C CDH18 Ensembl:ENSG00000145526 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs776114639 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20677,RMVar_hsa_circ_22171,RMVar_hsa_circ_22668,RMVar_hsa_circ_12854,RMVar_hsa_circ_23481,RMVar_hsa_circ_20964 28752 RMVar_ID_28752 Human_SNP_ID_223713142 A-to-I Human chr5 - 19715942 19715942 19715942 GTAGTAGTGCATGCCTGTAATCCCAGCTACTCAGGATGCTGAGCCAGAGAGAATCGCTTGAACCC GTAGTAGTGCATGCCTGTAATCCCAGCTACTCCGGATGCTGAGCCAGAGAGAATCGCTTGAACCC T G CDH18 Ensembl:ENSG00000145526 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1382202234 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20677,RMVar_hsa_circ_22171,RMVar_hsa_circ_22668,RMVar_hsa_circ_12854,RMVar_hsa_circ_23481,RMVar_hsa_circ_20964 28753 RMVar_ID_28753 Human_SNP_ID_223748853 A-to-I Human chr5 - 19858291 19858291 19858291 GAAGGCTGTGAAACCTGTATCCCCAACTCATTATCTTAACCCAGACATTTCTTTCTATTGATTCC GAAGGCTGTGAAACCTGTATCCCCAACTCATTGTCTTAACCCAGACATTTCTTTCTATTGATTCC T C CDH18 Ensembl:ENSG00000145526 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1335783374 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20677,RMVar_hsa_circ_22171,RMVar_hsa_circ_10857,RMVar_hsa_circ_332392 28754 RMVar_ID_28754 Human_SNP_ID_223774096 A-to-I Human chr5 - 19962602 19962602 19962602 CCAGCCAACTTTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAAGCTGGTTTCAT CCAGCCAACTTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAAGCTGGTTTCAT T C CDH18 Ensembl:ENSG00000145526 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1407720794 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20677,RMVar_hsa_circ_22171,RMVar_hsa_circ_10857,RMVar_hsa_circ_332392 28755 RMVar_ID_28755 Human_SNP_ID_223774413 A-to-I Human chr5 - 19963818 19963818 19963818 TTCTCCCTCCATCATGATTGTTAAGTTTCTTGAGGCATCCCCAGCCATGCAGAACTGTGAGTCGA TTCTCCCTCCATCATGATTGTTAAGTTTCTTGGGGCATCCCCAGCCATGCAGAACTGTGAGTCGA T C CDH18 Ensembl:ENSG00000145526 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs967679033 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20677,RMVar_hsa_circ_22171,RMVar_hsa_circ_10857,RMVar_hsa_circ_332392 28756 RMVar_ID_28756 Human_SNP_ID_223832406 A-to-I Human chr5 - 20199772 20199772 20199772 AGCATGGGAGAAACCACCCCCATGATTCAATTACCTCCTATTGGGTTCTTCCCATGACATGTAAG AGCATGGGAGAAACCACCCCCATGATTCAATTTCCTCCTATTGGGTTCTTCCCATGACATGTAAG T A CDH18 Ensembl:ENSG00000145526 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1255155868 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47574 28757 RMVar_ID_28757 Human_SNP_ID_223832407 A-to-I Human chr5 - 20199772 20199772 20199772 AGCATGGGAGAAACCACCCCCATGATTCAATTACCTCCTATTGGGTTCTTCCCATGACATGTAAG AGCATGGGAGAAACCACCCCCATGATTCAATTGCCTCCTATTGGGTTCTTCCCATGACATGTAAG T C CDH18 Ensembl:ENSG00000145526 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1255155868 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47574 28758 RMVar_ID_28758 Human_SNP_ID_223832467 A-to-I Human chr5 - 20199970 20199970 20199970 AGGAAAGAGTTTTACTTGATTCACAGTTGCATATGGCCGGGGAGGCCTCAGGAAATCGAGAATCA AGGAAAGAGTTTTACTTGATTCACAGTTGCATGTGGCCGGGGAGGCCTCAGGAAATCGAGAATCA T C CDH18 Ensembl:ENSG00000145526 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1023773424 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47574 28759 RMVar_ID_28759 Human_SNP_ID_223886721 A-to-I Human chr5 - 20415201 20415201 20415201 TTTGTATTTTAGTAGAGACAGGGTTTCACCATATTGCCCAGGCTGGCCTCAAACTCCTGAGCTCA TTTGTATTTTAGTAGAGACAGGGTTTCACCATGTTGCCCAGGCTGGCCTCAAACTCCTGAGCTCA T C CDH18 Ensembl:ENSG00000145526 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs929876408 Functional Loss SNV dbSNP153 33..33 33 - - - 28760 RMVar_ID_28760 Human_SNP_ID_223906401 A-to-I Human chr5 - 20493166 20493166 20493166 TTTTGTATTTTTAGTAGAGAAGGGACATCACCATGTTGGCCAGGCTGGTCACAAACTCCTAACCT TTTTGTATTTTTAGTAGAGAAGGGACATCACCGTGTTGGCCAGGCTGGTCACAAACTCCTAACCT T C CDH18 Ensembl:ENSG00000145526 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs557462635 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_230563 28761 RMVar_ID_28761 Human_SNP_ID_223906402 A-to-I Human chr5 - 20493166 20493166 20493166 TTTTGTATTTTTAGTAGAGAAGGGACATCACCATGTTGGCCAGGCTGGTCACAAACTCCTAACCT TTTTGTATTTTTAGTAGAGAAGGGACATCACCCTGTTGGCCAGGCTGGTCACAAACTCCTAACCT T G CDH18 Ensembl:ENSG00000145526 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs557462635 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_230563 28762 RMVar_ID_28762 Human_SNP_ID_223906410 A-to-I Human chr5 - 20493202 20493202 20493202 TGGAACTACAGGCAAGTGTCACCATGCTGGCTAGTTTTTTGTATTTTTAGTAGAGAAGGGACATC TGGAACTACAGGCAAGTGTCACCATGCTGGCTGGTTTTTTGTATTTTTAGTAGAGAAGGGACATC T C CDH18 Ensembl:ENSG00000145526 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1329592365 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_230563 28763 RMVar_ID_28763 Human_SNP_ID_223906415 A-to-I Human chr5 - 20493220 20493220 20493220 CTCAGCCTCCTGAGTAGCTGGAACTACAGGCAAGTGTCACCATGCTGGCTAGTTTTTTGTATTTT CTCAGCCTCCTGAGTAGCTGGAACTACAGGCATGTGTCACCATGCTGGCTAGTTTTTTGTATTTT T A CDH18 Ensembl:ENSG00000145526 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1437232615 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_230563 28764 RMVar_ID_28764 Human_SNP_ID_223910942 A-to-I Human chr5 - 20509678 20509678 20509678 ATGATGGCTCATGCCTGTAATCCCAGCACTTTAGGAGGCCAAGGCGGGCGGATCACAAGGTCAGG ATGATGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGCGGATCACAAGGTCAGG T C CDH18 Ensembl:ENSG00000145526 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1474089837 Functional Loss SNV dbSNP153 33..33 33 - - - 28765 RMVar_ID_28765 Human_SNP_ID_223922164 A-to-I Human chr5 - 20552883 20552883 20552883 GTGCATGATGGAGCACGCCTGTAGTCTCGGCTACTCAGGAGGCTGAGACAGGAGAATTGCTTGAA GTGCATGATGGAGCACGCCTGTAGTCTCGGCTGCTCAGGAGGCTGAGACAGGAGAATTGCTTGAA T C CDH18 Ensembl:ENSG00000145526 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1207813551 Functional Loss SNV dbSNP153 33..33 33 - - - 28766 RMVar_ID_28766 Human_SNP_ID_223922167 A-to-I Human chr5 - 20552893 20552893 20552893 AAAATTAGCCGTGCATGATGGAGCACGCCTGTAGTCTCGGCTACTCAGGAGGCTGAGACAGGAGA AAAATTAGCCGTGCATGATGGAGCACGCCTGTCGTCTCGGCTACTCAGGAGGCTGAGACAGGAGA T G CDH18 Ensembl:ENSG00000145526 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1296293721 Functional Loss SNV dbSNP153 33..33 33 - - - 28767 RMVar_ID_28767 Human_SNP_ID_224142931 A-to-I Human chr5 + 21462724 21462724 21462724 TCAAGCAATTTTCCTGCCTCAGCCCCCCAAGTAGCTGGGACGACAGGTGTATGCCACCACGCCCA TCAAGCAATTTTCCTGCCTCAGCCCCCCAAGTTGCTGGGACGACAGGTGTATGCCACCACGCCCA A T GUSBP1 Ensembl:ENSG00000183666 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1402979857 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17415910 RMVar_hsa_circ_46242,RMVar_hsa_circ_119679,RMVar_hsa_circ_230566,RMVar_hsa_circ_91454,RMVar_hsa_circ_230565 28768 RMVar_ID_28768 Human_SNP_ID_224143376 A-to-I Human chr5 + 21464397 21464397 21464397 GAGGCTGAGATGAGAGGGTCACTTGAGCCCAGAGGTTGAGGCTGCAGTGAGCTATGATCATGCCA GAGGCTGAGATGAGAGGGTCACTTGAGCCCAGTGGTTGAGGCTGCAGTGAGCTATGATCATGCCA A T GUSBP1 Ensembl:ENSG00000183666 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1175228323 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_46242,RMVar_hsa_circ_119679,RMVar_hsa_circ_230566,RMVar_hsa_circ_91454,RMVar_hsa_circ_230565 28769 RMVar_ID_28769 Human_SNP_ID_224143759 A-to-I Human chr5 + 21465883 21465883 21465883 CCTGGCCAACGTGATGAAACCCTGTCTCTACTAAAGATACAAAAATTAACCCGGTGTGGGTGGCG CCTGGCCAACGTGATGAAACCCTGTCTCTACTGAAGATACAAAAATTAACCCGGTGTGGGTGGCG A G GUSBP1 Ensembl:ENSG00000183666 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1214122965 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_46242,RMVar_hsa_circ_119679,RMVar_hsa_circ_230566,RMVar_hsa_circ_91454,RMVar_hsa_circ_230565 28770 RMVar_ID_28770 Human_SNP_ID_224144133 A-to-I Human chr5 + 21467250 21467250 21467250 GCGTGCACCACCATGCCCGGATAATTTGTTGTATTTCTAGTAGAGACGGGGTTTCACCATGCTGG GCGTGCACCACCATGCCCGGATAATTTGTTGTTTTTCTAGTAGAGACGGGGTTTCACCATGCTGG A T GUSBP1 Ensembl:ENSG00000183666 Pseudogene intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1297967998 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15555570 RMVar_hsa_circ_46242,RMVar_hsa_circ_119679,RMVar_hsa_circ_230566,RMVar_hsa_circ_91454,RMVar_hsa_circ_230565 28771 RMVar_ID_28771 Human_SNP_ID_224146281 A-to-I Human chr5 + 21473355 21473355 21473355 AGGTGTCCTTTTCTCTCCCCATGATACTTCACAGTTCAACCCAATGGAAATGGATTGAAAGAGTG AGGTGTCCTTTTCTCTCCCCATGATACTTCACGGTTCAACCCAATGGAAATGGATTGAAAGAGTG A G GUSBP1 Ensembl:ENSG00000183666 Pseudogene intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs894890429 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_46242,RMVar_hsa_circ_119679,RMVar_hsa_circ_230566,RMVar_hsa_circ_91454,RMVar_hsa_circ_230565 28772 RMVar_ID_28772 Human_SNP_ID_224151652 A-to-I Human chr5 + 21491319 21491319 21491319 CTCCCTAAGCCCTGGTCTCTCTTGCCTCCTGCAGGGCTGGTGAATTACCAGATCTCCGTCAAGTG CTCCCTAAGCCCTGGTCTCTCTTGCCTCCTGCCGGGCTGGTGAATTACCAGATCTCCGTCAAGTG A C GUSBP1 Ensembl:ENSG00000183666 Pseudogene intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1201505486 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5611509 RMVar_hsa_circ_46242,RMVar_hsa_circ_119679,RMVar_hsa_circ_230566,RMVar_hsa_circ_91454,RMVar_hsa_circ_230565,RMVar_hsa_circ_304021,RMVar_hsa_circ_312411,RMVar_hsa_circ_376720,RMVar_hsa_circ_294943 28773 RMVar_ID_28773 Human_SNP_ID_224165380 A-to-I Human chr5 + 21539502 21539498 21539502 ACATTATGCTATGTAAATAAGCCAGGAACAGAAAGACATACTGCCTGATCTCACTTACACGTGGA ACATTATGCTATGTAAATAAGCCAGGAAC____AGACATACTGCCTGATCTCACTTACACGTGGA CAGAA C GUSBP1 Ensembl:ENSG00000183666 Pseudogene intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1299927234 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_18518805 28774 RMVar_ID_28774 Human_SNP_ID_224165380 A-to-I Human chr5 + 21539501 21539498 21539502 GACATTATGCTATGTAAATAAGCCAGGAACAGAAAGACATACTGCCTGATCTCACTTACACGTGG GACATTATGCTATGTAAATAAGCCAGGAAC____AGACATACTGCCTGATCTCACTTACACGTGG CAGAA C GUSBP1 Ensembl:ENSG00000183666 Pseudogene intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1299927234 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_18518805 28775 RMVar_ID_28775 Human_SNP_ID_224253919 A-to-I Human chr5 - 21883795 21883795 21883795 CAACATCACTTGTCCCACCAAACTTCAGCACAACTACTCCATCTGAAAGTTTTGCCAGCCATTCA CAACATCACTTGTCCCACCAAACTTCAGCACAGCTACTCCATCTGAAAGTTTTGCCAGCCATTCA T C CDH12 Ensembl:ENSG00000154162 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1397783864 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3898,RMVar_hsa_circ_334499 28776 RMVar_ID_28776 Human_SNP_ID_224348067 A-to-I Human chr5 - 22270855 22270855 22270855 CCTGGCCAACATGGTGAAACCCTATCTGTACTAAATACACAAAAAATTAGCTGGGCTTCGTAGTA CCTGGCCAACATGGTGAAACCCTATCTGTACTGAATACACAAAAAATTAGCTGGGCTTCGTAGTA T C CDH12 Ensembl:ENSG00000154162 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1008534725 Functional Loss SNV dbSNP153 33..33 33 - - - 28777 RMVar_ID_28777 Human_SNP_ID_224478694 A-to-I Human chr5 - 22779635 22779635 22779635 TCAGATCTCATGAGAACTCACTCACTATCACAAGACCGGCATGGGGAAACTGCCTCCATGATCCA TCAGATCTCATGAGAACTCACTCACTATCACAGGACCGGCATGGGGAAACTGCCTCCATGATCCA T C CDH12 Ensembl:ENSG00000154162 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs552156488 Functional Loss SNV dbSNP153 33..33 33 - - - 28778 RMVar_ID_28778 Human_SNP_ID_224951414 A-to-I Human chr5 - 24569891 24569891 24569891 GGCGTCGTGGCACGCGCCTGTCGTCCCATGCAACTCGGGAGGCTGAGACAGCAGAATTTCTTGAA GGCGTCGTGGCACGCGCCTGTCGTCCCATGCATCTCGGGAGGCTGAGACAGCAGAATTTCTTGAA T A CDH10 Ensembl:ENSG00000040731 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs767946035 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86715,RMVar_hsa_circ_230590,RMVar_hsa_circ_26524,RMVar_hsa_circ_28397,RMVar_hsa_circ_230593,RMVar_hsa_circ_323022,RMVar_hsa_circ_230594 28779 RMVar_ID_28779 Human_SNP_ID_225298111 A-to-I Human chr5 - 25910227 25910227 25910227 TTGAAAGAAATGCTCCTGATTTCACTCCAAGGAAAGCCTATCTTGGGAGTTAGTCTGTCATGCTG TTGAAAGAAATGCTCCTGATTTCACTCCAAGGGAAGCCTATCTTGGGAGTTAGTCTGTCATGCTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1169825342 Functional Loss SNV dbSNP153 33..33 33 - - - 28780 RMVar_ID_28780 Human_SNP_ID_225298113 A-to-I Human chr5 - 25910230 25910230 25910230 TCATTGAAAGAAATGCTCCTGATTTCACTCCAAGGAAAGCCTATCTTGGGAGTTAGTCTGTCATG TCATTGAAAGAAATGCTCCTGATTTCACTCCAGGGAAAGCCTATCTTGGGAGTTAGTCTGTCATG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs942831160 Functional Loss SNV dbSNP153 33..33 33 - - - 28781 RMVar_ID_28781 Human_SNP_ID_225298310 A-to-I Human chr5 + 25910828 25910828 25910828 AACTGGCCCGACAGAAGAAAGAGAGTGAGGCTATGGAGTGGCAGCAGAAGGCCCAGATGGTACAG AACTGGCCCGACAGAAGAAAGAGAGTGAGGCTGTGGAGTGGCAGCAGAAGGCCCAGATGGTACAG A G MSNP1 Ensembl:ENSG00000251593 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs964252428 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26525741 28782 RMVar_ID_28782 Human_SNP_ID_225593406 A-to-I Human chr5 - 26974181 26974181 26974181 CTGAAGTGCAGTGGCGCAATCTCATCTCTGCAACCACTGTCTCCCAGGTTCAAGCGATTCTCTAG CTGAAGTGCAGTGGCGCAATCTCATCTCTGCAGCCACTGTCTCCCAGGTTCAAGCGATTCTCTAG T C CDH9 Ensembl:ENSG00000113100 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1320847142 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33276,RMVar_hsa_circ_60448 28783 RMVar_ID_28783 Human_SNP_ID_297648313 A-to-I Human chr6 - 135027893 135027893 135027893 GAGTGTGGTGGCACGCATCTTTGATCCCAGCTACTTGGGAGGCTGAGGTGGGAAGATTGCTTGAG GAGTGTGGTGGCACGCATCTTTGATCCCAGCTGCTTGGGAGGCTGAGGTGGGAAGATTGCTTGAG T C HBS1L Ensembl:ENSG00000112339 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924560312 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1393579 RMVar_hsa_circ_2717,RMVar_hsa_circ_268962 28784 RMVar_ID_28784 Human_SNP_ID_297650031 A-to-I Human chr6 - 135035338 135035338 135035338 TCAAGTGATTCTCCTGACTCAGCCTCCTGAGTAGCTGGGACTACAGGTGCATGTCACCACGCCCA TCAAGTGATTCTCCTGACTCAGCCTCCTGAGTGGCTGGGACTACAGGTGCATGTCACCACGCCCA T C HBS1L Ensembl:ENSG00000112339 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1234897641 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2717,RMVar_hsa_circ_268962 28785 RMVar_ID_28785 Human_SNP_ID_297692150 A-to-I Human chr6 + 135208655 135208655 135208655 CTTCTGCCTTGACCTCCCAAAGTGCTGGGATTACAGGCAGGAGCCACCCTGCCCAGCCTGAAGTA CTTCTGCCTTGACCTCCCAAAGTGCTGGGATTGCAGGCAGGAGCCACCCTGCCCAGCCTGAAGTA A G MYB Ensembl:ENSG00000118513 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs537729823 Functional Loss SNV dbSNP153 33..33 33 - - - 28786 RMVar_ID_28786 Human_SNP_ID_297714202 A-to-I Human chr6 - 135304762 135304762 135304762 GATCAGGATGGTCTTCACTTTTTGGAGATGGAATCTCGCTCTGTCTCACAGGTTGGAGTGCCGTG GATCAGGATGGTCTTCACTTTTTGGAGATGGAGTCTCGCTCTGTCTCACAGGTTGGAGTGCCGTG T C AHI1 Ensembl:ENSG00000135541 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1441931001 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 28787 RMVar_ID_28787 Human_SNP_ID_297715505 A-to-I Human chr6 - 135311067 135311067 135311067 AAACTCCTAGCCTCAAGTGATCTGCGCGCCTCAGCCTCCCAAAGTGCTGCGATGACAAGTGTGAG AAACTCCTAGCCTCAAGTGATCTGCGCGCCTCTGCCTCCCAAAGTGCTGCGATGACAAGTGTGAG T A AHI1 Ensembl:ENSG00000135541 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1346100211 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15655047 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 28788 RMVar_ID_28788 Human_SNP_ID_297715535 A-to-I Human chr6 - 135311180 135311180 135311180 CTCCTGCCTCAGTCTCCCGAGTGGCTTGGACTACAGATGTGGGCCACCATGCCCTGCTAATGTTT CTCCTGCCTCAGTCTCCCGAGTGGCTTGGACTGCAGATGTGGGCCACCATGCCCTGCTAATGTTT T C AHI1 Ensembl:ENSG00000135541 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1040201002 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18854683 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 28789 RMVar_ID_28789 Human_SNP_ID_297715549 A-to-I Human chr6 - 135311249 135311249 135311249 CACCCAGGTTGGAGTGCAGTGATGGGATCCCAACTCACTGCAACCTCTGCCTTCCCAGTTCAAGT CACCCAGGTTGGAGTGCAGTGATGGGATCCCAGCTCACTGCAACCTCTGCCTTCCCAGTTCAAGT T C AHI1 Ensembl:ENSG00000135541 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs531737097 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 28790 RMVar_ID_28790 Human_SNP_ID_297719125 A-to-I Human chr6 - 135326698 135326698 135326698 AAATTGGCTGAGCATGGTGGCGGGTGCCTGTAATCCCAGCTACTCAGGAGGCCAAGGCAGGAGAA AAATTGGCTGAGCATGGTGGCGGGTGCCTGTAGTCCCAGCTACTCAGGAGGCCAAGGCAGGAGAA T C AHI1 Ensembl:ENSG00000135541 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1316967498 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38246,RMVar_hsa_circ_58003,RMVar_hsa_circ_291676,RMVar_hsa_circ_330785,RMVar_hsa_circ_339594,RMVar_hsa_circ_327263,RMVar_hsa_circ_72687,RMVar_hsa_circ_70681,RMVar_hsa_circ_11419,RMVar_hsa_circ_299373,RMVar_hsa_circ_241634,RMVar_hsa_circ_335844,RMVar_hsa_circ_340014,RMVar_hsa_circ_95389,RMVar_hsa_circ_270586,RMVar_hsa_circ_64241,RMVar_hsa_circ_241635,RMVar_hsa_circ_241637,RMVar_hsa_circ_241636,RMVar_hsa_circ_241639,RMVar_hsa_circ_285958 28791 RMVar_ID_28791 Human_SNP_ID_297734091 A-to-I Human chr6 - 135386858 135386858 135386858 GGGAGGCCGAGGTGGGCCAATCAGCTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGATGA GGGAGGCCGAGGTGGGCCAATCAGCTGAGGTCTGGAGTTCAAGACCAGCCTGGCCAACATGATGA T A AHI1 Ensembl:ENSG00000135541 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs535736617 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 28792 RMVar_ID_28792 Human_SNP_ID_297734092 A-to-I Human chr6 - 135386858 135386858 135386858 GGGAGGCCGAGGTGGGCCAATCAGCTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGATGA GGGAGGCCGAGGTGGGCCAATCAGCTGAGGTCGGGAGTTCAAGACCAGCCTGGCCAACATGATGA T C AHI1 Ensembl:ENSG00000135541 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs535736617 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 28793 RMVar_ID_28793 Human_SNP_ID_297738801 A-to-I Human chr6 - 135406133 135406133 135406133 GTGAGGTCTTACCTAGGTTGCAGAATGCTTTTAGGTATTGCTGTGGCAGCAACATGCAGTCAAGT GTGAGGTCTTACCTAGGTTGCAGAATGCTTTTTGGTATTGCTGTGGCAGCAACATGCAGTCAAGT T A AHI1 Ensembl:ENSG00000135541 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1206972067 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1056,RMVar_hsa_circ_38246,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_335844,RMVar_hsa_circ_95389,RMVar_hsa_circ_270586,RMVar_hsa_circ_64241,RMVar_hsa_circ_265840,RMVar_hsa_circ_241635,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_241644,RMVar_hsa_circ_241642,RMVar_hsa_circ_318450,RMVar_hsa_circ_241649,RMVar_hsa_circ_241640,RMVar_hsa_circ_104679,RMVar_hsa_circ_241650,RMVar_hsa_circ_330346,RMVar_hsa_circ_359317,RMVar_hsa_circ_373891,RMVar_hsa_circ_327762,RMVar_hsa_circ_51360,RMVar_hsa_circ_309864,RMVar_hsa_circ_306936,RMVar_hsa_circ_34289,RMVar_hsa_circ_39963,RMVar_hsa_circ_7523,RMVar_hsa_circ_50614,RMVar_hsa_circ_241651,RMVar_hsa_circ_241653,RMVar_hsa_circ_241652,RMVar_hsa_circ_96524,RMVar_hsa_circ_268221,RMVar_hsa_circ_1190,RMVar_hsa_circ_2366,RMVar_hsa_circ_241655 28794 RMVar_ID_28794 Human_SNP_ID_297738958 A-to-I Human chr6 - 135406940 135406940 135406940 GAGAGCGTTGGTAAATCTCATTCTAAGTTTTCAGATCCAGAAATTTGATTTTATCAGTGCATCCA GAGAGCGTTGGTAAATCTCATTCTAAGTTTTCGGATCCAGAAATTTGATTTTATCAGTGCATCCA T C AHI1 Ensembl:ENSG00000135541 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924332380 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1056,RMVar_hsa_circ_38246,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_335844,RMVar_hsa_circ_95389,RMVar_hsa_circ_270586,RMVar_hsa_circ_64241,RMVar_hsa_circ_265840,RMVar_hsa_circ_241635,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_241644,RMVar_hsa_circ_241642,RMVar_hsa_circ_318450,RMVar_hsa_circ_241649,RMVar_hsa_circ_241640,RMVar_hsa_circ_104679,RMVar_hsa_circ_241650,RMVar_hsa_circ_330346,RMVar_hsa_circ_359317,RMVar_hsa_circ_373891,RMVar_hsa_circ_327762,RMVar_hsa_circ_51360,RMVar_hsa_circ_309864,RMVar_hsa_circ_306936,RMVar_hsa_circ_34289,RMVar_hsa_circ_39963,RMVar_hsa_circ_7523,RMVar_hsa_circ_50614,RMVar_hsa_circ_241651,RMVar_hsa_circ_241653,RMVar_hsa_circ_241652,RMVar_hsa_circ_96524,RMVar_hsa_circ_268221,RMVar_hsa_circ_1190,RMVar_hsa_circ_2366,RMVar_hsa_circ_241655 28795 RMVar_ID_28795 Human_SNP_ID_297759757 A-to-I Human chr6 - 135493120 135493120 135493120 GTGGCGCACACCTGTAATCCCAGCCACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCTGGGA GTGGCGCACACCTGTAATCCCAGCCACTCGGGGGGCTGAGGCAGGAGAATCGCTTGAACCTGGGA T C AHI1 Ensembl:ENSG00000135541 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs566686429 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_169976 RMVar_hsa_circ_1056,RMVar_hsa_circ_72687,RMVar_hsa_circ_7344,RMVar_hsa_circ_318450,RMVar_hsa_circ_29745,RMVar_hsa_circ_8034,RMVar_hsa_circ_47144,RMVar_hsa_circ_86620,RMVar_hsa_circ_241671,RMVar_hsa_circ_241675,RMVar_hsa_circ_241674,RMVar_hsa_circ_320544,RMVar_hsa_circ_307493,RMVar_hsa_circ_331674 28796 RMVar_ID_28796 Human_SNP_ID_297759758 A-to-I Human chr6 - 135493120 135493120 135493120 GTGGCGCACACCTGTAATCCCAGCCACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCTGGGA GTGGCGCACACCTGTAATCCCAGCCACTCGGGCGGCTGAGGCAGGAGAATCGCTTGAACCTGGGA T G AHI1 Ensembl:ENSG00000135541 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs566686429 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_169976 RMVar_hsa_circ_1056,RMVar_hsa_circ_72687,RMVar_hsa_circ_7344,RMVar_hsa_circ_318450,RMVar_hsa_circ_29745,RMVar_hsa_circ_8034,RMVar_hsa_circ_47144,RMVar_hsa_circ_86620,RMVar_hsa_circ_241671,RMVar_hsa_circ_241675,RMVar_hsa_circ_241674,RMVar_hsa_circ_320544,RMVar_hsa_circ_307493,RMVar_hsa_circ_331674 28797 RMVar_ID_28797 Human_SNP_ID_297759762 A-to-I Human chr6 - 135493131 135493131 135493131 AGCTGGGTGTGGTGGCGCACACCTGTAATCCCAGCCACTCGGGAGGCTGAGGCAGGAGAATCGCT AGCTGGGTGTGGTGGCGCACACCTGTAATCCCGGCCACTCGGGAGGCTGAGGCAGGAGAATCGCT T C AHI1 Ensembl:ENSG00000135541 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs962056900 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_169976 RMVar_hsa_circ_1056,RMVar_hsa_circ_72687,RMVar_hsa_circ_7344,RMVar_hsa_circ_318450,RMVar_hsa_circ_29745,RMVar_hsa_circ_8034,RMVar_hsa_circ_47144,RMVar_hsa_circ_86620,RMVar_hsa_circ_241671,RMVar_hsa_circ_241675,RMVar_hsa_circ_241674,RMVar_hsa_circ_320544,RMVar_hsa_circ_307493,RMVar_hsa_circ_331674 28798 RMVar_ID_28798 Human_SNP_ID_297759774 A-to-I Human chr6 - 135493192 135493192 135493192 GAGTTCAAGACCAGCCTGGCCAACATGATGAAACCCTGTCTCTACTAAAAATACAAAAATTAGCT GAGTTCAAGACCAGCCTGGCCAACATGATGAAGCCCTGTCTCTACTAAAAATACAAAAATTAGCT T C AHI1 Ensembl:ENSG00000135541 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs915793793 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1056,RMVar_hsa_circ_72687,RMVar_hsa_circ_7344,RMVar_hsa_circ_318450,RMVar_hsa_circ_29745,RMVar_hsa_circ_8034,RMVar_hsa_circ_47144,RMVar_hsa_circ_86620,RMVar_hsa_circ_241671,RMVar_hsa_circ_241675,RMVar_hsa_circ_241674,RMVar_hsa_circ_320544,RMVar_hsa_circ_307493,RMVar_hsa_circ_331674 28799 RMVar_ID_28799 Human_SNP_ID_297759919 A-to-I Human chr6 - 135493795 135493795 135493795 CAAGTGATCCACCCGCCTTATCCTTCCCAAGTATTGGGATTACAGACATGAGCCACGGCGCCCAG CAAGTGATCCACCCGCCTTATCCTTCCCAAGTGTTGGGATTACAGACATGAGCCACGGCGCCCAG T C AHI1 Ensembl:ENSG00000135541 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893405086 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25966364 RMVar_hsa_circ_1056,RMVar_hsa_circ_72687,RMVar_hsa_circ_7344,RMVar_hsa_circ_318450,RMVar_hsa_circ_29745,RMVar_hsa_circ_8034,RMVar_hsa_circ_47144,RMVar_hsa_circ_86620,RMVar_hsa_circ_241671,RMVar_hsa_circ_241675,RMVar_hsa_circ_241674,RMVar_hsa_circ_320544,RMVar_hsa_circ_307493,RMVar_hsa_circ_331674 28800 RMVar_ID_28800 Human_SNP_ID_297759956 A-to-I Human chr6 - 135493943 135493943 135493943 CACATTTCAGGTTCAAGCGATTTTCCTGCCTCAGCCTCCCCAGTAGCTGGGATTACAGGCACCCA CACATTTCAGGTTCAAGCGATTTTCCTGCCTCGGCCTCCCCAGTAGCTGGGATTACAGGCACCCA T C AHI1 Ensembl:ENSG00000135541 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,cerebellum - 29129909,30559470 RNA-Seq:(High) rs546696396 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1056,RMVar_hsa_circ_72687,RMVar_hsa_circ_7344,RMVar_hsa_circ_318450,RMVar_hsa_circ_29745,RMVar_hsa_circ_8034,RMVar_hsa_circ_47144,RMVar_hsa_circ_86620,RMVar_hsa_circ_241671,RMVar_hsa_circ_241675,RMVar_hsa_circ_241674,RMVar_hsa_circ_320544,RMVar_hsa_circ_307493,RMVar_hsa_circ_331674 28801 RMVar_ID_28801 Human_SNP_ID_297759959 A-to-I Human chr6 - 135493961 135493961 135493961 TTGGCTCCCTGCAACCTCCACATTTCAGGTTCAAGCGATTTTCCTGCCTCAGCCTCCCCAGTAGC TTGGCTCCCTGCAACCTCCACATTTCAGGTTCCAGCGATTTTCCTGCCTCAGCCTCCCCAGTAGC T G AHI1 Ensembl:ENSG00000135541 Protein coding intron GSE47997;GSE100210;GSE107867 K562 cells&HepG2 cells;HepG2 cell line;ASD brains,cerebellum - 23474544,29129909,30559470 RNA-Seq:(High) rs1354264679 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1056,RMVar_hsa_circ_72687,RMVar_hsa_circ_7344,RMVar_hsa_circ_318450,RMVar_hsa_circ_29745,RMVar_hsa_circ_8034,RMVar_hsa_circ_47144,RMVar_hsa_circ_86620,RMVar_hsa_circ_241671,RMVar_hsa_circ_241675,RMVar_hsa_circ_241674,RMVar_hsa_circ_320544,RMVar_hsa_circ_307493,RMVar_hsa_circ_331674 28802 RMVar_ID_28802 Human_SNP_ID_297759964 A-to-I Human chr6 - 135493980 135493980 135493980 GGAGCGCACTGGTGCAGTCTTGGCTCCCTGCAACCTCCACATTTCAGGTTCAAGCGATTTTCCTG GGAGCGCACTGGTGCAGTCTTGGCTCCCTGCAGCCTCCACATTTCAGGTTCAAGCGATTTTCCTG T C AHI1 Ensembl:ENSG00000135541 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs928985299 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1056,RMVar_hsa_circ_72687,RMVar_hsa_circ_7344,RMVar_hsa_circ_318450,RMVar_hsa_circ_29745,RMVar_hsa_circ_8034,RMVar_hsa_circ_47144,RMVar_hsa_circ_86620,RMVar_hsa_circ_241671,RMVar_hsa_circ_241675,RMVar_hsa_circ_241674,RMVar_hsa_circ_320544,RMVar_hsa_circ_307493,RMVar_hsa_circ_331674 28803 RMVar_ID_28803 Human_SNP_ID_297964763 A-to-I Human chr6 - 136339160 136339160 136339160 CCTGGGTGACAAGAGTGAAACTCCATCTCAAAAAAAAAAAACTTTTGCGTTTAGTTTGAGATACT CCTGGGTGACAAGAGTGAAACTCCATCTCAAAGAAAAAAAACTTTTGCGTTTAGTTTGAGATACT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs977796118 Functional Loss SNV dbSNP153 33..33 33 - - - 28804 RMVar_ID_28804 Human_SNP_ID_297965371 A-to-I Human chr6 - 136341415 136341415 136341415 TGATGGGGCTGGGTTCCGTGGCTTACACTGTAATCCGAGCACTTTGAGAGGCCAAGGCAGGAGGA TGATGGGGCTGGGTTCCGTGGCTTACACTGTAGTCCGAGCACTTTGAGAGGCCAAGGCAGGAGGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334653077 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8632251,Human_RBP_ID_15659034 28805 RMVar_ID_28805 Human_SNP_ID_297970871 A-to-I Human chr6 - 136365791 136365791 136365791 GCCCTCACTAAAGGGCAGAGCACCTTTAGTGAAGGTAGAAGAAGCCACAGTTGAAGAGCGGACAC GCCCTCACTAAAGGGCAGAGCACCTTTAGTGATGGTAGAAGAAGCCACAGTTGAAGAGCGGACAC T A MAP7 Ensembl:ENSG00000135525 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs763486220 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_816331,Human_Splice_Rec_816365,Human_Splice_Rec_816395,Human_Splice_Rec_816427,Human_Splice_Rec_816461,Human_Splice_Rec_816497,Human_Splice_Rec_816531,Human_Splice_Rec_816563,Human_Splice_Rec_816591 RMVar_hsa_circ_59035,RMVar_hsa_circ_269019,RMVar_hsa_circ_366845,RMVar_hsa_circ_266974,RMVar_hsa_circ_71377,RMVar_hsa_circ_75044,RMVar_hsa_circ_265139,RMVar_hsa_circ_45100 28806 RMVar_ID_28806 Human_SNP_ID_297989552 A-to-I Human chr6 - 136448707 136448707 136448707 GGAGTCCTTTATAAGAATTCATAGGCATTGCTAGGCACGGTGGCCACGCCTGTAATCCCAGCACT GGAGTCCTTTATAAGAATTCATAGGCATTGCTGGGCACGGTGGCCACGCCTGTAATCCCAGCACT T C MAP7 Ensembl:ENSG00000135525 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1282860264 Functional Loss SNV dbSNP153 33..33 33 - - - 28807 RMVar_ID_28807 Human_SNP_ID_298003515 A-to-I Human chr6 - 136509683 136509683 136509683 TGGTGGTGCATGTATGTATTCCCAGCTAACTCAGAAGGCTGAGGTGAAAGGATTGCTTGAGTCTG TGGTGGTGCATGTATGTATTCCCAGCTAACTCTGAAGGCTGAGGTGAAAGGATTGCTTGAGTCTG T A MAP7 Ensembl:ENSG00000135525 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs371750497 Functional Loss SNV dbSNP153 33..33 33 - - - 28808 RMVar_ID_28808 Human_SNP_ID_298010945 A-to-I Human chr6 - 136543601 136543601 136543601 TTGCCCAGGCTGGAGTGCAATGGCACAATCTCAGCTCACAGGAACCTCCTCCGCCTCCTGGGTTC TTGCCCAGGCTGGAGTGCAATGGCACAATCTCGGCTCACAGGAACCTCCTCCGCCTCCTGGGTTC T C MAP7 Ensembl:ENSG00000135525 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs972258526 Functional Loss SNV dbSNP153 33..33 33 - - - 28809 RMVar_ID_28809 Human_SNP_ID_298011037 A-to-I Human chr6 - 136544033 136544033 136544033 TCTGTAATCCGAACTACACAGGAGGCTGAGGCAGGAGAATTGTTTGAACCTGGGAGACGGAGGGT TCTGTAATCCGAACTACACAGGAGGCTGAGGCGGGAGAATTGTTTGAACCTGGGAGACGGAGGGT T C MAP7 Ensembl:ENSG00000135525 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1463458203 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2978611 28810 RMVar_ID_28810 Human_SNP_ID_298031869 A-to-I Human chr6 - 136634834 136634834 136634834 AGTCAGGTGTGGTGGCTCATGCCTGTAATCCCAGCACATTGGGATGCTGAGGTGAGTGGATCACT AGTCAGGTGTGGTGGCTCATGCCTGTAATCCCGGCACATTGGGATGCTGAGGTGAGTGGATCACT T C MAP3K5 Ensembl:ENSG00000197442 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1047420005 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8182,RMVar_hsa_circ_87272,RMVar_hsa_circ_241710,RMVar_hsa_circ_126061,RMVar_hsa_circ_241711,RMVar_hsa_circ_66632,RMVar_hsa_circ_371758,RMVar_hsa_circ_267793,RMVar_hsa_circ_241716,RMVar_hsa_circ_4763,RMVar_hsa_circ_102899,RMVar_hsa_circ_38131,RMVar_hsa_circ_104208,RMVar_hsa_circ_241719,RMVar_hsa_circ_321104,RMVar_hsa_circ_241721,RMVar_hsa_circ_47510,RMVar_hsa_circ_39793,RMVar_hsa_circ_313431,RMVar_hsa_circ_67118,RMVar_hsa_circ_241722,RMVar_hsa_circ_121711,RMVar_hsa_circ_241724,RMVar_hsa_circ_241727,RMVar_hsa_circ_327672,RMVar_hsa_circ_82073,RMVar_hsa_circ_265852,RMVar_hsa_circ_241725,RMVar_hsa_circ_377769,RMVar_hsa_circ_70722,RMVar_hsa_circ_277617,RMVar_hsa_circ_32055,RMVar_hsa_circ_241726 28811 RMVar_ID_28811 Human_SNP_ID_298031874 A-to-I Human chr6 - 136634862 136634862 136634862 AAAAAGAGAAGAAAAGAAATTATTCTGAAGTCAGGTGTGGTGGCTCATGCCTGTAATCCCAGCAC AAAAAGAGAAGAAAAGAAATTATTCTGAAGTCGGGTGTGGTGGCTCATGCCTGTAATCCCAGCAC T C MAP3K5 Ensembl:ENSG00000197442 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1367639770 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8182,RMVar_hsa_circ_87272,RMVar_hsa_circ_241710,RMVar_hsa_circ_126061,RMVar_hsa_circ_241711,RMVar_hsa_circ_66632,RMVar_hsa_circ_371758,RMVar_hsa_circ_267793,RMVar_hsa_circ_241716,RMVar_hsa_circ_4763,RMVar_hsa_circ_102899,RMVar_hsa_circ_38131,RMVar_hsa_circ_104208,RMVar_hsa_circ_241719,RMVar_hsa_circ_321104,RMVar_hsa_circ_241721,RMVar_hsa_circ_47510,RMVar_hsa_circ_39793,RMVar_hsa_circ_313431,RMVar_hsa_circ_67118,RMVar_hsa_circ_241722,RMVar_hsa_circ_121711,RMVar_hsa_circ_241724,RMVar_hsa_circ_241727,RMVar_hsa_circ_327672,RMVar_hsa_circ_82073,RMVar_hsa_circ_265852,RMVar_hsa_circ_241725,RMVar_hsa_circ_377769,RMVar_hsa_circ_70722,RMVar_hsa_circ_277617,RMVar_hsa_circ_32055,RMVar_hsa_circ_241726 28812 RMVar_ID_28812 Human_SNP_ID_298067781 A-to-I Human chr6 - 136789827 136789827 136789827 AAAATTAGCCAGGCATGGTGGTGCACACCTGTAGTCCTAGCTACTCAGGAGGCTGAGGCAGGATA AAAATTAGCCAGGCATGGTGGTGCACACCTGTTGTCCTAGCTACTCAGGAGGCTGAGGCAGGATA T A MAP3K5 Ensembl:ENSG00000197442 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1465671529 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25968479 RMVar_hsa_circ_126949,RMVar_hsa_circ_241748,RMVar_hsa_circ_241753,RMVar_hsa_circ_76299 28813 RMVar_ID_28813 Human_SNP_ID_298170579 A-to-I Human chr6 - 137216831 137216831 137216831 GTCACTTTTGTGAAGCCTTTCCTGACTCCCCTAGAAGAGACAAGCACCCCGGCCTTGCTTTTCAT GTCACTTTTGTGAAGCCTTTCCTGACTCCCCTGGAAGAGACAAGCACCCCGGCCTTGCTTTTCAT T C IFNGR1 Ensembl:ENSG00000027697 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1460094454 Functional Loss SNV dbSNP153 33..33 33 - - - 28814 RMVar_ID_28814 Human_SNP_ID_298475808 A-to-I Human chr6 - 138443609 138443609 138443609 TTGCTTAGACTGGTCTTGAACGCCTGAGTTCAAGTGATCCACCCACCTCAACTCTCCAATGTGCT TTGCTTAGACTGGTCTTGAACGCCTGAGTTCAGGTGATCCACCCACCTCAACTCTCCAATGTGCT T C NHSL1 Ensembl:ENSG00000135540 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1410875430 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_241796,RMVar_hsa_circ_53662,RMVar_hsa_circ_241798,RMVar_hsa_circ_298090,RMVar_hsa_circ_304313,RMVar_hsa_circ_291571,RMVar_hsa_circ_241797 28815 RMVar_ID_28815 Human_SNP_ID_298476395 A-to-I Human chr6 - 138446175 138446175 138446175 AAATTAGCAGGGCGTGGTGGCACGTGCGTGTAATCCCAGCTACTCTGGAGTCTGAGGCAGGAGAA AAATTAGCAGGGCGTGGTGGCACGTGCGTGTAGTCCCAGCTACTCTGGAGTCTGAGGCAGGAGAA T C NHSL1 Ensembl:ENSG00000135540 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1562278779 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_241796,RMVar_hsa_circ_53662,RMVar_hsa_circ_241798,RMVar_hsa_circ_298090,RMVar_hsa_circ_304313,RMVar_hsa_circ_291571,RMVar_hsa_circ_241797 28816 RMVar_ID_28816 Human_SNP_ID_298480977 A-to-I Human chr6 - 138464925 138464925 138464925 GTGGATCACCTGAGGCCAGGAGTTTGAGACCAACCTGGACAACATGGTGAAACCCTGTCTCTACT GTGGATCACCTGAGGCCAGGAGTTTGAGACCAGCCTGGACAACATGGTGAAACCCTGTCTCTACT T C NHSL1 Ensembl:ENSG00000135540 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs144352533 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_241798,RMVar_hsa_circ_298090,RMVar_hsa_circ_304313,RMVar_hsa_circ_241797,RMVar_hsa_circ_241801,RMVar_hsa_circ_302787,RMVar_hsa_circ_298089,RMVar_hsa_circ_241800 28817 RMVar_ID_28817 Human_SNP_ID_298480981 A-to-I Human chr6 - 138464940 138464939 138464940 GGGAGGCTGAGGTGGGTGGATCACCTGAGGCCAGGAGTTTGAGACCAACCTGGACAACATGGTGA GGGAGGCTGAGGTGGGTGGATCACCTGAGGCC_GGAGTTTGAGACCAACCTGGACAACATGGTGA CT C NHSL1 Ensembl:ENSG00000135540 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1443927239 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_241798,RMVar_hsa_circ_298090,RMVar_hsa_circ_304313,RMVar_hsa_circ_241797,RMVar_hsa_circ_241801,RMVar_hsa_circ_302787,RMVar_hsa_circ_298089,RMVar_hsa_circ_241800 28818 RMVar_ID_28818 Human_SNP_ID_298524159 A-to-I Human chr6 + 138650369 138650369 138650369 GGGGAGTAACGGGGGAGCCCAGCCTGCAGCCCACAGTTGTTCACAGCCATGAGGTCGCCGACTAG GGGGAGTAACGGGGGAGCCCAGCCTGCAGCCCGCAGTTGTTCACAGCCATGAGGTCGCCGACTAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs888909254 Functional Loss SNV dbSNP153 33..33 33 - - - 28819 RMVar_ID_28819 Human_SNP_ID_298533081 A-to-I Human chr6 - 138688060 138688060 138688060 GTAATCTCAGCTACTTGGGAGGCTGAGGCATGAGAATGACTTGAACCCAGGAGGTGGATATTGTA GTAATCTCAGCTACTTGGGAGGCTGAGGCATGCGAATGACTTGAACCCAGGAGGTGGATATTGTA T G NHSL1 Ensembl:ENSG00000135540 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs925147536 Functional Loss SNV dbSNP153 33..33 33 - - - 28820 RMVar_ID_28820 Human_SNP_ID_298533100 A-to-I Human chr6 - 138688134 138688134 138688134 CAGCCTGGCCAACATGGCGAAACTCTGTCTCTACTAAAAATACAAAAATTAGCTGGGCATAGGGG CAGCCTGGCCAACATGGCGAAACTCTGTCTCTTCTAAAAATACAAAAATTAGCTGGGCATAGGGG T A NHSL1 Ensembl:ENSG00000135540 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1286097158 Functional Loss SNV dbSNP153 33..33 33 - - - 28821 RMVar_ID_28821 Human_SNP_ID_298545610 A-to-I Human chr6 - 138738878 138738878 138738878 TAGAGACAGAATTTCACCATGTTGACCAGACCAGTCTCGAACTCCTCACATCAAATGATCCTCCT TAGAGACAGAATTTCACCATGTTGACCAGACCGGTCTCGAACTCCTCACATCAAATGATCCTCCT T C CCDC28A-AS1 Ensembl:ENSG00000279968 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs930484864 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15664420 28822 RMVar_ID_28822 Human_SNP_ID_298548384 A-to-I Human chr6 - 138750172 138750172 138750172 GCCTCCCTGATTTAAGCGATTCTCCTGCTTCAACCTCCCGAGTAGCTGGGACGACAGGCGCGCAC GCCTCCCTGATTTAAGCGATTCTCCTGCTTCAGCCTCCCGAGTAGCTGGGACGACAGGCGCGCAC T C CCDC28A-AS1 Ensembl:ENSG00000279968 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1324810976 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_Splice_Rec_817346,Human_Splice_Rec_817347,Human_Splice_Rec_817356 28823 RMVar_ID_28823 Human_SNP_ID_298548385 A-to-I Human chr6 - 138750172 138750172 138750172 GCCTCCCTGATTTAAGCGATTCTCCTGCTTCAACCTCCCGAGTAGCTGGGACGACAGGCGCGCAC GCCTCCCTGATTTAAGCGATTCTCCTGCTTCACCCTCCCGAGTAGCTGGGACGACAGGCGCGCAC T G CCDC28A-AS1 Ensembl:ENSG00000279968 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) - Functional Loss SNV HGVD 33..33 33 - - - Human_Splice_Rec_817346,Human_Splice_Rec_817347,Human_Splice_Rec_817356 28824 RMVar_ID_28824 Human_SNP_ID_298557963 A-to-I Human chr6 + 138790254 138790254 138790254 CTCACTGCAACCTGCTTCTCTGGGGTTCAAGCAATTCTCCTGCCTTAGCCTCCTGAGTAGCTGGG CTCACTGCAACCTGCTTCTCTGGGGTTCAAGCGATTCTCCTGCCTTAGCCTCCTGAGTAGCTGGG A G CCDC28A Ensembl:ENSG00000024862 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs904415974 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94584,RMVar_hsa_circ_110779,RMVar_hsa_circ_241810,RMVar_hsa_circ_241811,RMVar_hsa_circ_241812 28825 RMVar_ID_28825 Human_SNP_ID_298588847 A-to-I Human chr6 - 138914714 138914714 138914714 GAGTTGTTGCCCATCCTCCTGCAGTGCCTCCAAGACCACAGCCCTCACAGGTAATTCTCCAAGGT GAGTTGTTGCCCATCCTCCTGCAGTGCCTCCACGACCACAGCCCTCACAGGTAATTCTCCAAGGT T G REPS1 Ensembl:ENSG00000135597 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1419437713 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_251571,Human_RBP_ID_9402665,Human_RBP_ID_19132063 Human_Splice_Rec_817510,Human_Splice_Rec_817511,Human_Splice_Rec_817542,Human_Splice_Rec_817543,Human_Splice_Rec_817578,Human_Splice_Rec_817579,Human_Splice_Rec_817614,Human_Splice_Rec_817615,Human_Splice_Rec_817644,Human_Splice_Rec_817645,Human_Splice_Rec_817680,Human_Splice_Rec_817681,Human_Splice_Rec_817692,Human_Splice_Rec_817693,Human_Splice_Rec_817724,Human_Splice_Rec_817725,Human_Splice_Rec_817762,Human_Splice_Rec_817763,Human_Splice_Rec_817798,Human_Splice_Rec_817799,Human_Splice_Rec_817811,Human_Splice_Rec_817819,Human_Splice_Rec_817830,Human_Splice_Rec_817831 RMVar_hsa_circ_4997,RMVar_hsa_circ_118933,RMVar_hsa_circ_241814,RMVar_hsa_circ_241815,RMVar_hsa_circ_283983,RMVar_hsa_circ_297201,RMVar_hsa_circ_330396,RMVar_hsa_circ_377424,RMVar_hsa_circ_294269,RMVar_hsa_circ_241819,RMVar_hsa_circ_241821,RMVar_hsa_circ_241822,RMVar_hsa_circ_241820,RMVar_hsa_circ_355471,RMVar_hsa_circ_127910,RMVar_hsa_circ_241826,RMVar_hsa_circ_111231,RMVar_hsa_circ_7673,RMVar_hsa_circ_241827,RMVar_hsa_circ_297745,RMVar_hsa_circ_241824,RMVar_hsa_circ_241825,RMVar_hsa_circ_352198,RMVar_hsa_circ_241829,RMVar_hsa_circ_241830,RMVar_hsa_circ_241828,RMVar_hsa_circ_241831,RMVar_hsa_circ_342406 28826 RMVar_ID_28826 Human_SNP_ID_298590526 A-to-I Human chr6 - 138921496 138921496 138921496 TAAGTCATGGGCTATGCCCAGATCGTTTTTATATTTTTTGAAGAGACAGGGTTTCACTATGTTGC TAAGTCATGGGCTATGCCCAGATCGTTTTTATGTTTTTTGAAGAGACAGGGTTTCACTATGTTGC T C REPS1 Ensembl:ENSG00000135597 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs990394991 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118933,RMVar_hsa_circ_294269,RMVar_hsa_circ_241822,RMVar_hsa_circ_127910,RMVar_hsa_circ_241826,RMVar_hsa_circ_111231,RMVar_hsa_circ_7673,RMVar_hsa_circ_241827,RMVar_hsa_circ_297745,RMVar_hsa_circ_241825,RMVar_hsa_circ_241829,RMVar_hsa_circ_241828,RMVar_hsa_circ_9683,RMVar_hsa_circ_3536,RMVar_hsa_circ_75801,RMVar_hsa_circ_8198,RMVar_hsa_circ_241832,RMVar_hsa_circ_359280,RMVar_hsa_circ_368474,RMVar_hsa_circ_346549,RMVar_hsa_circ_7320,RMVar_hsa_circ_241836,RMVar_hsa_circ_241837,RMVar_hsa_circ_241835,RMVar_hsa_circ_15455 28827 RMVar_ID_28827 Human_SNP_ID_298590528 A-to-I Human chr6 - 138921498 138921498 138921498 TATAAGTCATGGGCTATGCCCAGATCGTTTTTATATTTTTTGAAGAGACAGGGTTTCACTATGTT TATAAGTCATGGGCTATGCCCAGATCGTTTTTTTATTTTTTGAAGAGACAGGGTTTCACTATGTT T A REPS1 Ensembl:ENSG00000135597 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913481590 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118933,RMVar_hsa_circ_294269,RMVar_hsa_circ_241822,RMVar_hsa_circ_127910,RMVar_hsa_circ_241826,RMVar_hsa_circ_111231,RMVar_hsa_circ_7673,RMVar_hsa_circ_241827,RMVar_hsa_circ_297745,RMVar_hsa_circ_241825,RMVar_hsa_circ_241829,RMVar_hsa_circ_241828,RMVar_hsa_circ_9683,RMVar_hsa_circ_3536,RMVar_hsa_circ_75801,RMVar_hsa_circ_8198,RMVar_hsa_circ_241832,RMVar_hsa_circ_359280,RMVar_hsa_circ_368474,RMVar_hsa_circ_346549,RMVar_hsa_circ_7320,RMVar_hsa_circ_241836,RMVar_hsa_circ_241837,RMVar_hsa_circ_241835,RMVar_hsa_circ_15455 28828 RMVar_ID_28828 Human_SNP_ID_298590529 A-to-I Human chr6 - 138921498 138921498 138921498 TATAAGTCATGGGCTATGCCCAGATCGTTTTTATATTTTTTGAAGAGACAGGGTTTCACTATGTT TATAAGTCATGGGCTATGCCCAGATCGTTTTTGTATTTTTTGAAGAGACAGGGTTTCACTATGTT T C REPS1 Ensembl:ENSG00000135597 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913481590 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118933,RMVar_hsa_circ_294269,RMVar_hsa_circ_241822,RMVar_hsa_circ_127910,RMVar_hsa_circ_241826,RMVar_hsa_circ_111231,RMVar_hsa_circ_7673,RMVar_hsa_circ_241827,RMVar_hsa_circ_297745,RMVar_hsa_circ_241825,RMVar_hsa_circ_241829,RMVar_hsa_circ_241828,RMVar_hsa_circ_9683,RMVar_hsa_circ_3536,RMVar_hsa_circ_75801,RMVar_hsa_circ_8198,RMVar_hsa_circ_241832,RMVar_hsa_circ_359280,RMVar_hsa_circ_368474,RMVar_hsa_circ_346549,RMVar_hsa_circ_7320,RMVar_hsa_circ_241836,RMVar_hsa_circ_241837,RMVar_hsa_circ_241835,RMVar_hsa_circ_15455 28829 RMVar_ID_28829 Human_SNP_ID_298595919 A-to-I Human chr6 - 138943565 138943565 138943565 AACACTGTTTTAATATTTCAGGATCTGCAGCTAAAGAGTTTTTTACAAAATCAAAACTTCCTATT AACACTGTTTTAATATTTCAGGATCTGCAGCTCAAGAGTTTTTTACAAAATCAAAACTTCCTATT T G REPS1 Ensembl:ENSG00000135597 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs748201305 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_817494,Human_Splice_Rec_817495,Human_Splice_Rec_817564,Human_Splice_Rec_817565,Human_Splice_Rec_817600,Human_Splice_Rec_817601,Human_Splice_Rec_817714,Human_Splice_Rec_817715,Human_Splice_Rec_817746,Human_Splice_Rec_817747,Human_Splice_Rec_817784,Human_Splice_Rec_817785,Human_Splice_Rec_817836,Human_Splice_Rec_817837,Human_Splice_Rec_817850,Human_Splice_Rec_817851 RMVar_hsa_circ_118933,RMVar_hsa_circ_241826,RMVar_hsa_circ_111231,RMVar_hsa_circ_241827,RMVar_hsa_circ_75801,RMVar_hsa_circ_8198,RMVar_hsa_circ_241832,RMVar_hsa_circ_359280,RMVar_hsa_circ_346549,RMVar_hsa_circ_7320,RMVar_hsa_circ_241836,RMVar_hsa_circ_241837,RMVar_hsa_circ_121144,RMVar_hsa_circ_270769,RMVar_hsa_circ_35437,RMVar_hsa_circ_273351,RMVar_hsa_circ_366607,RMVar_hsa_circ_273075,RMVar_hsa_circ_241840,RMVar_hsa_circ_241841,RMVar_hsa_circ_303581,RMVar_hsa_circ_241839,RMVar_hsa_circ_270376,RMVar_hsa_circ_241843,RMVar_hsa_circ_22218,RMVar_hsa_circ_241844,RMVar_hsa_circ_241842 28830 RMVar_ID_28830 Human_SNP_ID_298602211 A-to-I Human chr6 - 138969561 138969561 138969561 AGCCTTGCTGGGTACGGTGGCTCATGGCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGATGGA AGCCTTGCTGGGTACGGTGGCTCATGGCTGTATTCCCAGCACTTTGGGAGGCCGAGGCAGATGGA T A REPS1 Ensembl:ENSG00000135597 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs568612710 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118933,RMVar_hsa_circ_241827 28831 RMVar_ID_28831 Human_SNP_ID_299062202 A-to-I Human chr6 - 140865669 140865669 140865669 CCACCACGCTTGGCTAATTTTGTAGTTTTAGTAGAGATGGGGTTTCTCCATGTTGGTCAGGCTGG CCACCACGCTTGGCTAATTTTGTAGTTTTAGTGGAGATGGGGTTTCTCCATGTTGGTCAGGCTGG T C AL035446.2 Ensembl:ENSG00000285875 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1291292806 Functional Loss SNV dbSNP153 33..33 33 - - - 28832 RMVar_ID_28832 Human_SNP_ID_299358639 A-to-I Human chr6 - 142062753 142062753 142062753 TCTGGGGCATCACCAACAACTTCAAATTCAACATCCTTTCCTAGGTCTTCACTATGAAGGATGTT TCTGGGGCATCACCAACAACTTCAAATTCAACTTCCTTTCCTAGGTCTTCACTATGAAGGATGTT T A NMBR Ensembl:ENSG00000135577 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs879047586 Functional Loss SNV dbSNP153 33..33 33 - - - 28833 RMVar_ID_28833 Human_SNP_ID_299358640 A-to-I Human chr6 - 142062753 142062753 142062753 TCTGGGGCATCACCAACAACTTCAAATTCAACATCCTTTCCTAGGTCTTCACTATGAAGGATGTT TCTGGGGCATCACCAACAACTTCAAATTCAACGTCCTTTCCTAGGTCTTCACTATGAAGGATGTT T C NMBR Ensembl:ENSG00000135577 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs879047586 Functional Loss SNV dbSNP153 33..33 33 - - - 28834 RMVar_ID_28834 Human_SNP_ID_299385779 A-to-I Human chr6 + 142170373 142170373 142170373 TCCAGAAACATGATCAAGTCCTTCTATACTGCAAGTCTTTTGATAGATGTCATAACAGTATTTGG TCCAGAAACATGATCAAGTCCTTCTATACTGCCAGTCTTTTGATAGATGTCATAACAGTATTTGG A C VTA1 Ensembl:ENSG00000009844 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749410880 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_950091,Human_RBP_ID_2010057,Human_RBP_ID_9401190,Human_RBP_ID_22462891,Human_RBP_ID_26354445,Human_RBP_ID_27088705,Human_RBP_ID_27828971 Human_Splice_Rec_818306,Human_Splice_Rec_818307,Human_Splice_Rec_818318,Human_Splice_Rec_818319,Human_Splice_Rec_818328,Human_Splice_Rec_818329,Human_Splice_Rec_818342,Human_Splice_Rec_818343,Human_Splice_Rec_818351 Human_miRNA_ID_1247717,Human_miRNA_ID_2721646 RMVar_hsa_circ_95929,RMVar_hsa_circ_241858,RMVar_hsa_circ_277777,RMVar_hsa_circ_336745,RMVar_hsa_circ_359524,RMVar_hsa_circ_277550,RMVar_hsa_circ_241856,RMVar_hsa_circ_241857,RMVar_hsa_circ_241855,RMVar_hsa_circ_85478,RMVar_hsa_circ_241859,RMVar_hsa_circ_241860 28835 RMVar_ID_28835 Human_SNP_ID_299532711 A-to-I Human chr6 - 142757039 142757039 142757039 AAATGCAGATTGTGTTAAGTGTATGTGCATATATATGTATGCACACATATACACATATGTACAAA AAATGCAGATTGTGTTAAGTGTATGTGCATATGTATGTATGCACACATATACACATATGTACAAA T C HIVEP2 Ensembl:ENSG00000010818 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs925390720 Functional Loss SNV dbSNP153 33..33 33 - - - 28836 RMVar_ID_28836 Human_SNP_ID_299532712 A-to-I Human chr6 - 142757041 142757041 142757041 TCAAATGCAGATTGTGTTAAGTGTATGTGCATATATATGTATGCACACATATACACATATGTACA TCAAATGCAGATTGTGTTAAGTGTATGTGCATTTATATGTATGCACACATATACACATATGTACA T A HIVEP2 Ensembl:ENSG00000010818 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs946206651 Functional Loss SNV dbSNP153 33..33 33 - - - 28837 RMVar_ID_28837 Human_SNP_ID_299537856 A-to-I Human chr6 - 142776629 142776629 142776629 TACTTGGGAGCCTGAGGTGGGAGGATCGCCTGAGCTCAGGGAGGTCGAGGCTGCAGTGAGCAGTG TACTTGGGAGCCTGAGGTGGGAGGATCGCCTGTGCTCAGGGAGGTCGAGGCTGCAGTGAGCAGTG T A HIVEP2 Ensembl:ENSG00000010818 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1168462511 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57422,RMVar_hsa_circ_44275,RMVar_hsa_circ_351917,RMVar_hsa_circ_241880,RMVar_hsa_circ_334083 28838 RMVar_ID_28838 Human_SNP_ID_299573845 A-to-I Human chr6 - 142935366 142935366 142935366 TTTTGCACTTTTTGTGGAGACAGGGTTTTGCCATGTTGCCCAGGCTGATCTCCAACTCCTAGGCT TTTTGCACTTTTTGTGGAGACAGGGTTTTGCCGTGTTGCCCAGGCTGATCTCCAACTCCTAGGCT T C HIVEP2 Ensembl:ENSG00000010818 Protein coding intron GSE107867 ASD brains,cerebellum;ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1045763107 Functional Loss SNV dbSNP153 33..33 33 - - - 28839 RMVar_ID_28839 Human_SNP_ID_299573976 A-to-I Human chr6 - 142936055 142936055 142936055 CAGGCTGGAGTGCAGTGGCGCGATCACGGTTCACTGCAACCTCGACCTCCTGGGCTCAAATGATC CAGGCTGGAGTGCAGTGGCGCGATCACGGTTCGCTGCAACCTCGACCTCCTGGGCTCAAATGATC T C HIVEP2 Ensembl:ENSG00000010818 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1321821179 Functional Loss SNV dbSNP153 33..33 33 - - - 28840 RMVar_ID_28840 Human_SNP_ID_299574068 A-to-I Human chr6 - 142936357 142936357 142936357 TGAAACCCCATCTCTACTAAAATTCAAAAATTAGCCTGGTGTGGTGGCACGTGCCTGTAGTCCCA TGAAACCCCATCTCTACTAAAATTCAAAAATTTGCCTGGTGTGGTGGCACGTGCCTGTAGTCCCA T A HIVEP2 Ensembl:ENSG00000010818 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432137793 Functional Loss SNV dbSNP153 33..33 33 - - - 28841 RMVar_ID_28841 Human_SNP_ID_299616142 A-to-I Human chr6 + 143113509 143113509 143113509 CCTGTAGTCCCAGCTACTTGGTAGGCTGAGGCAGGTGAATCGCTTGAACTCAGGAGGCGGAGGTT CCTGTAGTCCCAGCTACTTGGTAGGCTGAGGCGGGTGAATCGCTTGAACTCAGGAGGCGGAGGTT A G AIG1 Ensembl:ENSG00000146416 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs770861057 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_376715 28842 RMVar_ID_28842 Human_SNP_ID_299694240 A-to-I Human chr6 - 143450034 143450034 143450034 TAAAGGGGGCTTTCAACAGAATGCTGTGTGCTAGCGAGCTTCTTAACTGGGAAAAAAAGTTTGTT TAAAGGGGGCTTTCAACAGAATGCTGTGTGCTGGCGAGCTTCTTAACTGGGAAAAAAAGTTTGTT T C ADAT2 Ensembl:ENSG00000189007 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1179449293 Functional Loss SNV dbSNP153 33..33 33 - - - 28843 RMVar_ID_28843 Human_SNP_ID_299708443 A-to-I Human chr6 + 143513012 143513012 143513012 CTTTTCTTTTTTAGTAGAGACAGGGTTTCACCATGTTGGACAAGCTGGTCTCAAACTCTTGACCT CTTTTCTTTTTTAGTAGAGACAGGGTTTCACCGTGTTGGACAAGCTGGTCTCAAACTCTTGACCT A G HSALNG0054037 RNACentral:URS0000EBD54B lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs566961460 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_241906 28844 RMVar_ID_28844 Human_SNP_ID_299869483 A-to-I Human chr6 + 144200850 144200850 144200850 CACCAATGAGCGAGTCATCAATGTTACCTTCTATCCTACTGACCATCTTCCCCTCCACCTCCAGG CACCAATGAGCGAGTCATCAATGTTACCTTCTGTCCTACTGACCATCTTCCCCTCCACCTCCAGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1462580470 Functional Loss SNV dbSNP153 33..33 33 - - - 28845 RMVar_ID_28845 Human_SNP_ID_299869493 A-to-I Human chr6 + 144200895 144200895 144200895 TCTTCCCCTCCACCTCCAGGTACAGCCCGTCCATGATCTCCCAGATCTTGTAGATGTCGGAAAAC TCTTCCCCTCCACCTCCAGGTACAGCCCGTCCGTGATCTCCCAGATCTTGTAGATGTCGGAAAAC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs748237014 Functional Loss SNV dbSNP153 33..33 33 - - - 28846 RMVar_ID_28846 Human_SNP_ID_299869494 A-to-I Human chr6 + 144200895 144200895 144200895 TCTTCCCCTCCACCTCCAGGTACAGCCCGTCCATGATCTCCCAGATCTTGTAGATGTCGGAAAAC TCTTCCCCTCCACCTCCAGGTACAGCCCGTCCTTGATCTCCCAGATCTTGTAGATGTCGGAAAAC A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs748237014 Functional Loss SNV dbSNP153 33..33 33 - - - 28847 RMVar_ID_28847 Human_SNP_ID_299869498 A-to-I Human chr6 + 144200905 144200905 144200905 CACCTCCAGGTACAGCCCGTCCATGATCTCCCAGATCTTGTAGATGTCGGAAAACATCTCATCGT CACCTCCAGGTACAGCCCGTCCATGATCTCCCGGATCTTGTAGATGTCGGAAAACATCTCATCGT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs567622531 Functional Loss SNV dbSNP153 33..33 33 - - - 28848 RMVar_ID_28848 Human_SNP_ID_299869499 A-to-I Human chr6 + 144200905 144200905 144200905 CACCTCCAGGTACAGCCCGTCCATGATCTCCCAGATCTTGTAGATGTCGGAAAACATCTCATCGT CACCTCCAGGTACAGCCCGTCCATGATCTCCCTGATCTTGTAGATGTCGGAAAACATCTCATCGT A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs567622531 Functional Loss SNV dbSNP153 33..33 33 - - - 28849 RMVar_ID_28849 Human_SNP_ID_299994967 A-to-I Human chr6 + 144732787 144732787 144732787 CAGGCTGGAGTGTAGTGGTGAAATCACGGCCCACTGCACATCAACGTCCCAGGATCAAGTGATCA CAGGCTGGAGTGTAGTGGTGAAATCACGGCCCGCTGCACATCAACGTCCCAGGATCAAGTGATCA A G UTRN Ensembl:ENSG00000152818 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917391699 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113273,RMVar_hsa_circ_266103,RMVar_hsa_circ_241927,RMVar_hsa_circ_122016,RMVar_hsa_circ_241933,RMVar_hsa_circ_102797,RMVar_hsa_circ_241937,RMVar_hsa_circ_107311,RMVar_hsa_circ_241950,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_101489,RMVar_hsa_circ_111050,RMVar_hsa_circ_107129,RMVar_hsa_circ_88162,RMVar_hsa_circ_241964,RMVar_hsa_circ_8868,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_108582,RMVar_hsa_circ_241975,RMVar_hsa_circ_95859,RMVar_hsa_circ_241977,RMVar_hsa_circ_125753,RMVar_hsa_circ_63968,RMVar_hsa_circ_241979,RMVar_hsa_circ_81705,RMVar_hsa_circ_100668,RMVar_hsa_circ_241980,RMVar_hsa_circ_241983,RMVar_hsa_circ_77748,RMVar_hsa_circ_241984,RMVar_hsa_circ_87648,RMVar_hsa_circ_74391,RMVar_hsa_circ_28940,RMVar_hsa_circ_241988,RMVar_hsa_circ_90589,RMVar_hsa_circ_73724,RMVar_hsa_circ_70114,RMVar_hsa_circ_80350,RMVar_hsa_circ_241989,RMVar_hsa_circ_109685,RMVar_hsa_circ_241995,RMVar_hsa_circ_241996,RMVar_hsa_circ_96163,RMVar_hsa_circ_126152,RMVar_hsa_circ_101294,RMVar_hsa_circ_241997,RMVar_hsa_circ_241998,RMVar_hsa_circ_241999,RMVar_hsa_circ_72791,RMVar_hsa_circ_66800,RMVar_hsa_circ_363469,RMVar_hsa_circ_364091,RMVar_hsa_circ_362351,RMVar_hsa_circ_55580,RMVar_hsa_circ_53931,RMVar_hsa_circ_242004,RMVar_hsa_circ_61465,RMVar_hsa_circ_315085,RMVar_hsa_circ_354778,RMVar_hsa_circ_373894,RMVar_hsa_circ_352102,RMVar_hsa_circ_69818,RMVar_hsa_circ_242006,RMVar_hsa_circ_42432,RMVar_hsa_circ_242005 28850 RMVar_ID_28850 Human_SNP_ID_300248686 A-to-I Human chr6 - 145787779 145787779 145787779 TAGCAGTCAACTTCTAGCTCAATGGAATTGTTATGTCTCCTGGTAGAAACATTTATCCCTCTGGA TAGCAGTCAACTTCTAGCTCAATGGAATTGTTGTGTCTCCTGGTAGAAACATTTATCCCTCTGGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs921279421 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_242034 28851 RMVar_ID_28851 Human_SNP_ID_300248731 A-to-I Human chr6 - 145787944 145787944 145787944 CCCCCCCTAGGGATATCTTGTATTCCAGACATACTCGTCCTTACCTCTATTGTAGAATAGCAGTC CCCCCCCTAGGGATATCTTGTATTCCAGACATGCTCGTCCTTACCTCTATTGTAGAATAGCAGTC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1024706832 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_242034 28852 RMVar_ID_28852 Human_SNP_ID_300248763 A-to-I Human chr6 - 145788063 145788063 145788063 CCTGATGGAGTAACCCAAATGTCTATTCCTGTAGGATCTCAGCAATTTGCAGCCCTGCCTGGATT CCTGATGGAGTAACCCAAATGTCTATTCCTGTGGGATCTCAGCAATTTGCAGCCCTGCCTGGATT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1022919036 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_242034 28853 RMVar_ID_28853 Human_SNP_ID_300341853 A-to-I Human chr6 + 146180041 146180041 146180041 TATGGTGGTGTGCACCTGTGGCCCCAGCTACTAGGGAAGCTGAGGAGATTTGCTTGAACCTGGGA TATGGTGGTGTGCACCTGTGGCCCCAGCTACTGGGGAAGCTGAGGAGATTTGCTTGAACCTGGGA A G GRM1 Ensembl:ENSG00000152822 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1194902453 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_31044,RMVar_hsa_circ_267261,RMVar_hsa_circ_341254 28854 RMVar_ID_28854 Human_SNP_ID_300596376 A-to-I Human chr6 + 147247684 147247684 147247684 TTTCCTTGTCAGAATTTCTCCTACAATTCTGCATCTTTTGTTTCAATATTGTGATTAATTTTGTC TTTCCTTGTCAGAATTTCTCCTACAATTCTGCGTCTTTTGTTTCAATATTGTGATTAATTTTGTC A G STXBP5 Ensembl:ENSG00000164506 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs957220760 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3925,RMVar_hsa_circ_109277,RMVar_hsa_circ_283606,RMVar_hsa_circ_374354,RMVar_hsa_circ_304411,RMVar_hsa_circ_280408,RMVar_hsa_circ_281932,RMVar_hsa_circ_271544,RMVar_hsa_circ_242075,RMVar_hsa_circ_242077,RMVar_hsa_circ_242078,RMVar_hsa_circ_242079,RMVar_hsa_circ_242076,RMVar_hsa_circ_242074,RMVar_hsa_circ_41558,RMVar_hsa_circ_346405,RMVar_hsa_circ_278779,RMVar_hsa_circ_9435,RMVar_hsa_circ_31217,RMVar_hsa_circ_292115,RMVar_hsa_circ_242080,RMVar_hsa_circ_375328,RMVar_hsa_circ_283740,RMVar_hsa_circ_38937,RMVar_hsa_circ_242084,RMVar_hsa_circ_242085,RMVar_hsa_circ_242086 28855 RMVar_ID_28855 Human_SNP_ID_300614535 A-to-I Human chr6 + 147323521 147323521 147323521 TCAGGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTGCAGGTGCTCACCACCACACCCG TCAGGCGATTCTCCTGCCTCAGCCTCCCGAGTTGCTGGGATTGCAGGTGCTCACCACCACACCCG A T STXBP5 Ensembl:ENSG00000164506 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1319338818 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109277,RMVar_hsa_circ_304411,RMVar_hsa_circ_281932,RMVar_hsa_circ_242078,RMVar_hsa_circ_242079,RMVar_hsa_circ_9435,RMVar_hsa_circ_38937,RMVar_hsa_circ_297788,RMVar_hsa_circ_242086,RMVar_hsa_circ_370668,RMVar_hsa_circ_330798,RMVar_hsa_circ_242088,RMVar_hsa_circ_9901,RMVar_hsa_circ_242089,RMVar_hsa_circ_376337,RMVar_hsa_circ_242087,RMVar_hsa_circ_378666,RMVar_hsa_circ_57846,RMVar_hsa_circ_3875,RMVar_hsa_circ_242102,RMVar_hsa_circ_242100,RMVar_hsa_circ_242101,RMVar_hsa_circ_340359,RMVar_hsa_circ_297473,RMVar_hsa_circ_126011,RMVar_hsa_circ_107739,RMVar_hsa_circ_242104,RMVar_hsa_circ_242103,RMVar_hsa_circ_14404,RMVar_hsa_circ_372751,RMVar_hsa_circ_242112,RMVar_hsa_circ_313320,RMVar_hsa_circ_347639,RMVar_hsa_circ_23253,RMVar_hsa_circ_106640,RMVar_hsa_circ_242115,RMVar_hsa_circ_242116,RMVar_hsa_circ_242117,RMVar_hsa_circ_242114,RMVar_hsa_circ_242118,RMVar_hsa_circ_45607,RMVar_hsa_circ_344186,RMVar_hsa_circ_242120,RMVar_hsa_circ_242121,RMVar_hsa_circ_69615,RMVar_hsa_circ_82972,RMVar_hsa_circ_100319,RMVar_hsa_circ_372986,RMVar_hsa_circ_242122,RMVar_hsa_circ_242123,RMVar_hsa_circ_242124,RMVar_hsa_circ_319593,RMVar_hsa_circ_325519,RMVar_hsa_circ_44121,RMVar_hsa_circ_4725,RMVar_hsa_circ_242125,RMVar_hsa_circ_242126,RMVar_hsa_circ_323400,RMVar_hsa_circ_62581 28856 RMVar_ID_28856 Human_SNP_ID_300671361 A-to-I Human chr6 + 147565478 147565478 147565478 TGTGTTTGGATGCTGGTAGTTTTTTTTTTTTTAGACAGAGTCTCGCTCTGTCACCCAGGCTGGAG TGTGTTTGGATGCTGGTAGTTTTTTTTTTTTTGGACAGAGTCTCGCTCTGTCACCCAGGCTGGAG A G SAMD5 Ensembl:ENSG00000203727 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1371551891 Functional Loss SNV dbSNP153 33..33 33 - - - 28857 RMVar_ID_28857 Human_SNP_ID_300671362 A-to-I Human chr6 + 147565478 147565478 147565478 TGTGTTTGGATGCTGGTAGTTTTTTTTTTTTTAGACAGAGTCTCGCTCTGTCACCCAGGCTGGAG TGTGTTTGGATGCTGGTAGTTTTTTTTTTTTTTGACAGAGTCTCGCTCTGTCACCCAGGCTGGAG A T SAMD5 Ensembl:ENSG00000203727 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1371551891 Functional Loss SNV dbSNP153 33..33 33 - - - 28858 RMVar_ID_28858 Human_SNP_ID_300672201 A-to-I Human chr6 + 147569146 147569146 147569146 CAGCTACTAAGGCAGGAGAATGGCTTGAACCCAGGAGGTGGAGGTCGCAGTGAGCTGAGATCGCG CAGCTACTAAGGCAGGAGAATGGCTTGAACCCCGGAGGTGGAGGTCGCAGTGAGCTGAGATCGCG A C SAMD5 Ensembl:ENSG00000203727 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,31158229,32596459 RNA-Seq:(High) rs1266820752 Functional Loss SNV dbSNP153 33..33 33 - - - 28859 RMVar_ID_28859 Human_SNP_ID_300672202 A-to-I Human chr6 + 147569149 147569149 147569149 CTACTAAGGCAGGAGAATGGCTTGAACCCAGGAGGTGGAGGTCGCAGTGAGCTGAGATCGCGCCA CTACTAAGGCAGGAGAATGGCTTGAACCCAGGGGGTGGAGGTCGCAGTGAGCTGAGATCGCGCCA A G SAMD5 Ensembl:ENSG00000203727 Protein coding 3'UTR GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1225450376 Functional Loss SNV dbSNP153 33..33 33 - - - 28860 RMVar_ID_28860 Human_SNP_ID_300857737 A-to-I Human chr6 - 148343106 148343106 148343106 GCGGGCTCGGGCTCCGGCTCGGGCTCGGGCTCAGGCTCCGGCCCCGGGCCAGCTGCTCCCGCGTC GCGGGCTCGGGCTCCGGCTCGGGCTCGGGCTCGGGCTCCGGCCCCGGGCCAGCTGCTCCCGCGTC T C - - Other Unknown GSE107867 ASD brains,cerebellum;ASD brains,frontal_cortex;ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1290001689 Functional Loss SNV dbSNP153 33..33 33 - - - 28861 RMVar_ID_28861 Human_SNP_ID_300857738 A-to-I Human chr6 - 148343106 148343106 148343106 GCGGGCTCGGGCTCCGGCTCGGGCTCGGGCTCAGGCTCCGGCCCCGGGCCAGCTGCTCCCGCGTC GCGGGCTCGGGCTCCGGCTCGGGCTCGGGCTCCGGCTCCGGCCCCGGGCCAGCTGCTCCCGCGTC T G - - Other Unknown GSE107867 ASD brains,cerebellum;ASD brains,frontal_cortex;ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1290001689 Functional Loss SNV dbSNP153 33..33 33 - - - 28862 RMVar_ID_28862 Human_SNP_ID_300896514 A-to-I Human chr6 + 148491504 148491504 148491504 GTTGACCAGGTTGGTCTCGAACCTCTGACCTCAGGTGATTCACCCGCCTCGGCCTACCAAAGTAC GTTGACCAGGTTGGTCTCGAACCTCTGACCTCCGGTGATTCACCCGCCTCGGCCTACCAAAGTAC A C SASH1 Ensembl:ENSG00000111961 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1294439184 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113911,RMVar_hsa_circ_116836,RMVar_hsa_circ_109493,RMVar_hsa_circ_242150,RMVar_hsa_circ_242152,RMVar_hsa_circ_242151,RMVar_hsa_circ_55894 28863 RMVar_ID_28863 Human_SNP_ID_300901408 A-to-I Human chr6 + 148512164 148512164 148512164 CCTCAGCCTCCTGAGTAGCTGGGACTACAGGCACCCGCCACCACGCCCAGCTAATTTTTTGTATT CCTCAGCCTCCTGAGTAGCTGGGACTACAGGCGCCCGCCACCACGCCCAGCTAATTTTTTGTATT A G SASH1 Ensembl:ENSG00000111961 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs974012474 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113911,RMVar_hsa_circ_116836,RMVar_hsa_circ_109493,RMVar_hsa_circ_242150,RMVar_hsa_circ_242152,RMVar_hsa_circ_242151,RMVar_hsa_circ_55894 28864 RMVar_ID_28864 Human_SNP_ID_301125676 A-to-I Human chr6 - 149448125 149448125 149448125 GCCACCACATCTGGCTAACTTTTTGTATTTTTAGTAGAGATGGGGTTTCACCGTGTTAGCCAGGA GCCACCACATCTGGCTAACTTTTTGTATTTTTGGTAGAGATGGGGTTTCACCGTGTTAGCCAGGA T C ZC3H12D Ensembl:ENSG00000178199 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs905638683 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98660,RMVar_hsa_circ_242183 28865 RMVar_ID_28865 Human_SNP_ID_301125679 A-to-I Human chr6 - 149448141 149448137 149448141 GGGACTACAGGCGCCCGCCACCACATCTGGCTAACTTTTTGTATTTTTAGTAGAGATGGGGTTTC GGGACTACAGGCGCCCGCCACCACATCTGGCT____TTTTGTATTTTTAGTAGAGATGGGGTTTC AAGTT A ZC3H12D Ensembl:ENSG00000178199 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1247013982 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_98660,RMVar_hsa_circ_242183 28866 RMVar_ID_28866 Human_SNP_ID_301125786 A-to-I Human chr6 - 149448502 149448502 149448502 TCTGTCATCTGTCACCCAGGCTGGAGTGCAGTAGTGCAATCAGGGCTCACTGCAGCTTTGACTTC TCTGTCATCTGTCACCCAGGCTGGAGTGCAGTGGTGCAATCAGGGCTCACTGCAGCTTTGACTTC T C ZC3H12D Ensembl:ENSG00000178199 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1469425640 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_821905 RMVar_hsa_circ_98660,RMVar_hsa_circ_242183 28867 RMVar_ID_28867 Human_SNP_ID_301126011 A-to-I Human chr6 - 149449438 149449438 149449438 GCGAGACTCCGTCTTAAAAAAAAAAAAAAGACAGAGTCTCACTCTGTCACTCTGTCTGGAGTATA GCGAGACTCCGTCTTAAAAAAAAAAAAAAGACGGAGTCTCACTCTGTCACTCTGTCTGGAGTATA T C ZC3H12D Ensembl:ENSG00000178199 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1186294382 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98660,RMVar_hsa_circ_242183 28868 RMVar_ID_28868 Human_SNP_ID_301126041 A-to-I Human chr6 - 149449540 149449540 149449540 CCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCTGGGAGGCGGAGGTTGCAGTGAGT CCAGCTACTCAGGAGGCTGAGGCAGGAGAATCTCTTGAACCTGGGAGGCGGAGGTTGCAGTGAGT T A ZC3H12D Ensembl:ENSG00000178199 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs805027 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98660,RMVar_hsa_circ_242183 28869 RMVar_ID_28869 Human_SNP_ID_301126042 A-to-I Human chr6 - 149449540 149449540 149449540 CCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCTGGGAGGCGGAGGTTGCAGTGAGT CCAGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACCTGGGAGGCGGAGGTTGCAGTGAGT T C ZC3H12D Ensembl:ENSG00000178199 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs805027 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98660,RMVar_hsa_circ_242183 28870 RMVar_ID_28870 Human_SNP_ID_301126052 A-to-I Human chr6 - 149449576 149449576 149449576 AAATTTAGCCAGGCATGGTGGCATACACCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGA AAATTTAGCCAGGCATGGTGGCATACACCTGTGGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGA T C ZC3H12D Ensembl:ENSG00000178199 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs967430477 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98660,RMVar_hsa_circ_242183 28871 RMVar_ID_28871 Human_SNP_ID_301139170 A-to-I Human chr6 - 149502007 149502007 149502007 TGAGGCCGGAGGATCCCTTGAGGCCAGGAGTTAGAGGCTGCAGTGCACTGCGATTGTGCCTGTGA TGAGGCCGGAGGATCCCTTGAGGCCAGGAGTTGGAGGCTGCAGTGCACTGCGATTGTGCCTGTGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs574156443 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21276142,Human_RBP_ID_26532954 28872 RMVar_ID_28872 Human_SNP_ID_301139334 A-to-I Human chr6 - 149502680 149502680 149502680 GGAGTGCAGTGGCGCAATCTCAGCTTACTGCAACCTCCACCTCCTGGGTTCAAGCGATTCTACTG GGAGTGCAGTGGCGCAATCTCAGCTTACTGCAGCCTCCACCTCCTGGGTTCAAGCGATTCTACTG T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1455419428 Functional Loss SNV dbSNP153 33..33 33 - - - 28873 RMVar_ID_28873 Human_SNP_ID_301157932 A-to-I Human chr6 + 149578341 149578341 149578341 GGTCAGGAGTTAGCAAGACCAGCCCGGCCAATATGGTGAAACCCTATCTCTGCTAAAAATACAAA GGTCAGGAGTTAGCAAGACCAGCCCGGCCAATGTGGTGAAACCCTATCTCTGCTAAAAATACAAA A G GINM1 Ensembl:ENSG00000055211 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1203741689 Functional Loss SNV dbSNP153 33..33 33 - - - 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 28874 RMVar_ID_28874 Human_SNP_ID_301160872 A-to-I Human chr6 + 149591088 149591088 149591088 AGGCCAATGCGGGCGGATCACGAGGTCAGATCAAGACCATCCTGCCAACATGGTGAAACCCTGTC AGGCCAATGCGGGCGGATCACGAGGTCAGATCGAGACCATCCTGCCAACATGGTGAAACCCTGTC A G GINM1 Ensembl:ENSG00000055211 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1137089 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23068334 Human_miRNA_ID_1266187 RMVar_hsa_circ_242204 28875 RMVar_ID_28875 Human_SNP_ID_301160880 A-to-I Human chr6 + 149591102 149591102 149591102 GGATCACGAGGTCAGATCAAGACCATCCTGCCAACATGGTGAAACCCTGTCTCTACTAAAAAAAA GGATCACGAGGTCAGATCAAGACCATCCTGCCGACATGGTGAAACCCTGTCTCTACTAAAAAAAA A G GINM1 Ensembl:ENSG00000055211 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs112257475 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23068334 Human_miRNA_ID_141082,Human_miRNA_ID_418132 RMVar_hsa_circ_242204 28876 RMVar_ID_28876 Human_SNP_ID_301160884 A-to-I Human chr6 + 149591112 149591112 149591112 GTCAGATCAAGACCATCCTGCCAACATGGTGAAACCCTGTCTCTACTAAAAAAAATAAAAAAATT GTCAGATCAAGACCATCCTGCCAACATGGTGAGACCCTGTCTCTACTAAAAAAAATAAAAAAATT A G GINM1 Ensembl:ENSG00000055211 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs562899312 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_242204 28877 RMVar_ID_28877 Human_SNP_ID_301160890 A-to-I Human chr6 + 149591128 149591126 149591129 CCTGCCAACATGGTGAAACCCTGTCTCTACTAAAAAAAATAAAAAAATTAGCTGGGTGTGGCGGT CCTGCCAACATGGTGAAACCCTGTCTCTACT___AAAAATAAAAAAATTAGCTGGGTGTGGCGGT TAAA T GINM1 Ensembl:ENSG00000055211 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs369150777 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_242204 28878 RMVar_ID_28878 Human_SNP_ID_301160901 A-to-I Human chr6 + 149591137 149591137 149591137 ATGGTGAAACCCTGTCTCTACTAAAAAAAATAAAAAAATTAGCTGGGTGTGGCGGTGCACGCCTG ATGGTGAAACCCTGTCTCTACTAAAAAAAATATAAAAATTAGCTGGGTGTGGCGGTGCACGCCTG A T GINM1 Ensembl:ENSG00000055211 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1430137848 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_242204 28879 RMVar_ID_28879 Human_SNP_ID_301160917 A-to-I Human chr6 + 149591171 149591171 149591171 AAAATTAGCTGGGTGTGGCGGTGCACGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA AAAATTAGCTGGGTGTGGCGGTGCACGCCTGTGGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA A G GINM1 Ensembl:ENSG00000055211 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs1283319059 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_242204 28880 RMVar_ID_28880 Human_SNP_ID_301161459 A-to-I Human chr6 + 149593009 149593008 149593010 CACCCACCTAGACCTCCCAAAATGCTGGAATTACAGGCGTGAGCCACCATGCCCGGCCATGGTTG CACCCACCTAGACCTCCCAAAATGCTGGAATT__AGGCGTGAGCCACCATGCCCGGCCATGGTTG TAC T RPS18P9 Ensembl:ENSG00000220848 Pseudogene exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1211071099 Functional Loss DEL dbSNP153 33..34 33 - - - 28881 RMVar_ID_28881 Human_SNP_ID_301161460 A-to-I Human chr6 + 149593009 149593009 149593009 CACCCACCTAGACCTCCCAAAATGCTGGAATTACAGGCGTGAGCCACCATGCCCGGCCATGGTTG CACCCACCTAGACCTCCCAAAATGCTGGAATTGCAGGCGTGAGCCACCATGCCCGGCCATGGTTG A G RPS18P9 Ensembl:ENSG00000220848 Pseudogene exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs887334727 Functional Loss SNV dbSNP153 33..33 33 - - - 28882 RMVar_ID_28882 Human_SNP_ID_301161769 A-to-I Human chr6 - 149594369 149594369 149594369 TTGTTGTCCAGACCATTGGCTAGGACCTGGCTATATTTTCCATCCTTTACATCCTTCTGTCTGTT TTGTTGTCCAGACCATTGGCTAGGACCTGGCTGTATTTTCCATCCTTTACATCCTTCTGTCTGTT T C - - Other Unknown GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs989068653 Functional Loss SNV dbSNP153 33..33 33 - - - 28883 RMVar_ID_28883 Human_SNP_ID_301163376 A-to-I Human chr6 - 149600538 149600538 149600538 GCCTTCACCTCCTAGCCTCAAGCGATCCTCCCACCTTAGCCTCCTGAGTAGCTGGGACTACACAA GCCTTCACCTCCTAGCCTCAAGCGATCCTCCCGCCTTAGCCTCCTGAGTAGCTGGGACTACACAA T C KATNA1 Ensembl:ENSG00000186625 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1183437494 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_317264,RMVar_hsa_circ_338751,RMVar_hsa_circ_45518,RMVar_hsa_circ_35220,RMVar_hsa_circ_39207 28884 RMVar_ID_28884 Human_SNP_ID_301178378 A-to-I Human chr6 - 149662844 149662844 149662844 CTTCTGCTTCAACCTCCTGAGTAGCTAGGACTACAGATGCATGCCACCATACCTGGCTAATTTTT CTTCTGCTTCAACCTCCTGAGTAGCTAGGACTGCAGATGCATGCCACCATACCTGGCTAATTTTT T C LATS1 Ensembl:ENSG00000131023 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs565616587 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95226,RMVar_hsa_circ_125035,RMVar_hsa_circ_242220,RMVar_hsa_circ_90724,RMVar_hsa_circ_242221,RMVar_hsa_circ_242219 28885 RMVar_ID_28885 Human_SNP_ID_301178384 A-to-I Human chr6 - 149662865 149662865 149662865 AACTCCTGGGCTCCAGGAATCCTTCTGCTTCAACCTCCTGAGTAGCTAGGACTACAGATGCATGC AACTCCTGGGCTCCAGGAATCCTTCTGCTTCAGCCTCCTGAGTAGCTAGGACTACAGATGCATGC T C LATS1 Ensembl:ENSG00000131023 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs538677691 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95226,RMVar_hsa_circ_125035,RMVar_hsa_circ_242220,RMVar_hsa_circ_90724,RMVar_hsa_circ_242221,RMVar_hsa_circ_242219 28886 RMVar_ID_28886 Human_SNP_ID_301179145 A-to-I Human chr6 - 149666026 149666026 149666026 GCGACTGTCCTGCCTCAGCCTCCCAGGTAGCTAGGACTACAGGCGTGTGCTACCATGCCCAGCTA GCGACTGTCCTGCCTCAGCCTCCCAGGTAGCTGGGACTACAGGCGTGTGCTACCATGCCCAGCTA T C LATS1 Ensembl:ENSG00000131023 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1296096942 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15682752 RMVar_hsa_circ_95226,RMVar_hsa_circ_125035,RMVar_hsa_circ_242220,RMVar_hsa_circ_90724,RMVar_hsa_circ_242221,RMVar_hsa_circ_242219 28887 RMVar_ID_28887 Human_SNP_ID_301179290 A-to-I Human chr6 - 149666496 149666496 149666496 GTTCCGCCTCAGCCTCCCAGGTAGCTGGGACTACAGTTGCTCGCCACCACACCCGGGTAATTTTT GTTCCGCCTCAGCCTCCCAGGTAGCTGGGACTGCAGTTGCTCGCCACCACACCCGGGTAATTTTT T C LATS1 Ensembl:ENSG00000131023 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1376420868 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15682766 RMVar_hsa_circ_95226,RMVar_hsa_circ_125035,RMVar_hsa_circ_242220,RMVar_hsa_circ_90724,RMVar_hsa_circ_242221,RMVar_hsa_circ_242219 28888 RMVar_ID_28888 Human_SNP_ID_301179821 A-to-I Human chr6 - 149668534 149668534 149668534 CTACTCCAGACACAAGAGGATCACTTGAGCCCAGGAGTTTGAGGCTGTAGTGAGCTATAATCATA CTACTCCAGACACAAGAGGATCACTTGAGCCCGGGAGTTTGAGGCTGTAGTGAGCTATAATCATA T C LATS1 Ensembl:ENSG00000131023 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1293151721 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95226,RMVar_hsa_circ_125035,RMVar_hsa_circ_242220,RMVar_hsa_circ_90724,RMVar_hsa_circ_242221,RMVar_hsa_circ_242219 28889 RMVar_ID_28889 Human_SNP_ID_301179876 A-to-I Human chr6 - 149668717 149668717 149668717 TGACAGGCTGAATGCAGTGGCTTATGCCTGCAATCCCAGCACTTTGGGAGGCTGACGCAAGAGGA TGACAGGCTGAATGCAGTGGCTTATGCCTGCATTCCCAGCACTTTGGGAGGCTGACGCAAGAGGA T A LATS1 Ensembl:ENSG00000131023 Protein coding intron GSE38233;GSE107867 cultured B-cells;ASD brains,cerebellum - 24183664,30559470 RNA-Seq:(High) rs538042367 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22619334 RMVar_hsa_circ_95226,RMVar_hsa_circ_125035,RMVar_hsa_circ_242220,RMVar_hsa_circ_90724,RMVar_hsa_circ_242221,RMVar_hsa_circ_242219 28890 RMVar_ID_28890 Human_SNP_ID_301179877 A-to-I Human chr6 - 149668717 149668717 149668717 TGACAGGCTGAATGCAGTGGCTTATGCCTGCAATCCCAGCACTTTGGGAGGCTGACGCAAGAGGA TGACAGGCTGAATGCAGTGGCTTATGCCTGCAGTCCCAGCACTTTGGGAGGCTGACGCAAGAGGA T C LATS1 Ensembl:ENSG00000131023 Protein coding intron GSE38233;GSE107867 cultured B-cells;ASD brains,cerebellum - 24183664,30559470 RNA-Seq:(High) rs538042367 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22619334 RMVar_hsa_circ_95226,RMVar_hsa_circ_125035,RMVar_hsa_circ_242220,RMVar_hsa_circ_90724,RMVar_hsa_circ_242221,RMVar_hsa_circ_242219 28891 RMVar_ID_28891 Human_SNP_ID_301179878 A-to-I Human chr6 - 149668717 149668717 149668717 TGACAGGCTGAATGCAGTGGCTTATGCCTGCAATCCCAGCACTTTGGGAGGCTGACGCAAGAGGA TGACAGGCTGAATGCAGTGGCTTATGCCTGCACTCCCAGCACTTTGGGAGGCTGACGCAAGAGGA T G LATS1 Ensembl:ENSG00000131023 Protein coding intron GSE38233;GSE107867 cultured B-cells;ASD brains,cerebellum - 24183664,30559470 RNA-Seq:(High) rs538042367 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22619334 RMVar_hsa_circ_95226,RMVar_hsa_circ_125035,RMVar_hsa_circ_242220,RMVar_hsa_circ_90724,RMVar_hsa_circ_242221,RMVar_hsa_circ_242219 28892 RMVar_ID_28892 Human_SNP_ID_301180068 A-to-I Human chr6 - 149669497 149669497 149669497 CGTTGGCCTCCCAAAATGTTGGGATTGCAAGCATGAGCCTGCACCTGGCTTGTAGTTATTTTATA CGTTGGCCTCCCAAAATGTTGGGATTGCAAGCCTGAGCCTGCACCTGGCTTGTAGTTATTTTATA T G LATS1 Ensembl:ENSG00000131023 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1346272654 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17576503 RMVar_hsa_circ_95226,RMVar_hsa_circ_125035,RMVar_hsa_circ_242220,RMVar_hsa_circ_90724,RMVar_hsa_circ_242221,RMVar_hsa_circ_242219 28893 RMVar_ID_28893 Human_SNP_ID_301180105 A-to-I Human chr6 - 149669652 149669652 149669652 CGGGTTCAAGATTCTCCCGTGTCATCCTCCCAAGTAGCCTGGATTACAGGCACATGCCATCACGC CGGGTTCAAGATTCTCCCGTGTCATCCTCCCAGGTAGCCTGGATTACAGGCACATGCCATCACGC T C LATS1 Ensembl:ENSG00000131023 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984020716 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95226,RMVar_hsa_circ_125035,RMVar_hsa_circ_242220,RMVar_hsa_circ_90724,RMVar_hsa_circ_242221,RMVar_hsa_circ_242219 28894 RMVar_ID_28894 Human_SNP_ID_301180109 A-to-I Human chr6 - 149669676 149669676 149669676 CAGCTCACTGCAACCTCTGCCTCCCGGGTTCAAGATTCTCCCGTGTCATCCTCCCAAGTAGCCTG CAGCTCACTGCAACCTCTGCCTCCCGGGTTCAGGATTCTCCCGTGTCATCCTCCCAAGTAGCCTG T C LATS1 Ensembl:ENSG00000131023 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913605574 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95226,RMVar_hsa_circ_125035,RMVar_hsa_circ_242220,RMVar_hsa_circ_90724,RMVar_hsa_circ_242221,RMVar_hsa_circ_242219 28895 RMVar_ID_28895 Human_SNP_ID_301180117 A-to-I Human chr6 - 149669707 149669707 149669707 TCGCCCACGCTGGAGTGCAGGGTCGTGATCTCAGCTCACTGCAACCTCTGCCTCCCGGGTTCAAG TCGCCCACGCTGGAGTGCAGGGTCGTGATCTCGGCTCACTGCAACCTCTGCCTCCCGGGTTCAAG T C LATS1 Ensembl:ENSG00000131023 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1451618540 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95226,RMVar_hsa_circ_125035,RMVar_hsa_circ_242220,RMVar_hsa_circ_90724,RMVar_hsa_circ_242221,RMVar_hsa_circ_242219 28896 RMVar_ID_28896 Human_SNP_ID_301180184 A-to-I Human chr6 - 149670009 149670009 149670009 CTCCCCAACACCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACTGTGTTGGCCAGGC CTCCCCAACACCTGGCTAATTTTTGTATTTTTTGTAGAGACAGGGTTTCACTGTGTTGGCCAGGC T A LATS1 Ensembl:ENSG00000131023 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1321443456 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95226,RMVar_hsa_circ_125035,RMVar_hsa_circ_242220,RMVar_hsa_circ_90724,RMVar_hsa_circ_242221,RMVar_hsa_circ_242219 28897 RMVar_ID_28897 Human_SNP_ID_301180672 A-to-I Human chr6 - 149671996 149671996 149671996 TAATCCCAGCTACTCGGGAGGTGGAGACAGGAAAATAGCTTGAATCTGGGAGGAGGAGGTTGCAG TAATCCCAGCTACTCGGGAGGTGGAGACAGGAGAATAGCTTGAATCTGGGAGGAGGAGGTTGCAG T C LATS1 Ensembl:ENSG00000131023 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1051796511 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95226,RMVar_hsa_circ_125035,RMVar_hsa_circ_242220,RMVar_hsa_circ_90724,RMVar_hsa_circ_242221,RMVar_hsa_circ_242219 28898 RMVar_ID_28898 Human_SNP_ID_301180762 A-to-I Human chr6 - 149672294 149672294 149672294 GAGGGAGGAGAATCACTTGAACCTGGGAGGTAAAGATTGCAGTGAGCTAAGATTGTGCCACTGCA GAGGGAGGAGAATCACTTGAACCTGGGAGGTACAGATTGCAGTGAGCTAAGATTGTGCCACTGCA T G LATS1 Ensembl:ENSG00000131023 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941867972 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95226,RMVar_hsa_circ_125035,RMVar_hsa_circ_242220,RMVar_hsa_circ_90724,RMVar_hsa_circ_242221,RMVar_hsa_circ_242219 28899 RMVar_ID_28899 Human_SNP_ID_301180773 A-to-I Human chr6 - 149672351 149672351 149672351 AAAAAATTAGCCAGGCATGATGGCAGGCACCTATAAACTCCAGCTACTCAGGAGGCTGAGGGAGG AAAAAATTAGCCAGGCATGATGGCAGGCACCTGTAAACTCCAGCTACTCAGGAGGCTGAGGGAGG T C LATS1 Ensembl:ENSG00000131023 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1038168070 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25974091 RMVar_hsa_circ_95226,RMVar_hsa_circ_125035,RMVar_hsa_circ_242220,RMVar_hsa_circ_90724,RMVar_hsa_circ_242221,RMVar_hsa_circ_242219 28900 RMVar_ID_28900 Human_SNP_ID_301180862 A-to-I Human chr6 - 149672780 149672780 149672780 GCCACCATCCCAGTTAATTTTGTATTTTTAGTAAAGACTGGGTTTTACCATGTTGGTCAGGCTGG GCCACCATCCCAGTTAATTTTGTATTTTTAGTGAAGACTGGGTTTTACCATGTTGGTCAGGCTGG T C LATS1 Ensembl:ENSG00000131023 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs894066679 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95226,RMVar_hsa_circ_125035,RMVar_hsa_circ_242220,RMVar_hsa_circ_90724,RMVar_hsa_circ_242221,RMVar_hsa_circ_242219 28901 RMVar_ID_28901 Human_SNP_ID_301181448 A-to-I Human chr6 - 149675051 149675051 149675051 CATCATACCCAGCTAGTTTTTGTATTTTTAGTAGAGACGAGGTTTCACCGTGTTGGCCAGGATGG CATCATACCCAGCTAGTTTTTGTATTTTTAGTGGAGACGAGGTTTCACCGTGTTGGCCAGGATGG T C LATS1 Ensembl:ENSG00000131023 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1285113155 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95226,RMVar_hsa_circ_125035,RMVar_hsa_circ_242220,RMVar_hsa_circ_90724,RMVar_hsa_circ_242221,RMVar_hsa_circ_242219 28902 RMVar_ID_28902 Human_SNP_ID_301181469 A-to-I Human chr6 - 149675154 149675154 149675154 AGAGTGCAGTGGCGTGATCTCAGTTCACTACAACTTCTGCCTCCTGGGTTCAAGCAATTCTCGTG AGAGTGCAGTGGCGTGATCTCAGTTCACTACAGCTTCTGCCTCCTGGGTTCAAGCAATTCTCGTG T C LATS1 Ensembl:ENSG00000131023 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1291055667 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95226,RMVar_hsa_circ_125035,RMVar_hsa_circ_242220,RMVar_hsa_circ_90724,RMVar_hsa_circ_242221,RMVar_hsa_circ_242219 28903 RMVar_ID_28903 Human_SNP_ID_301181471 A-to-I Human chr6 - 149675157 149675157 149675157 GCTAGAGTGCAGTGGCGTGATCTCAGTTCACTACAACTTCTGCCTCCTGGGTTCAAGCAATTCTC GCTAGAGTGCAGTGGCGTGATCTCAGTTCACTGCAACTTCTGCCTCCTGGGTTCAAGCAATTCTC T C LATS1 Ensembl:ENSG00000131023 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1458838398 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95226,RMVar_hsa_circ_125035,RMVar_hsa_circ_242220,RMVar_hsa_circ_90724,RMVar_hsa_circ_242221,RMVar_hsa_circ_242219 28904 RMVar_ID_28904 Human_SNP_ID_301183212 A-to-I Human chr6 - 149681990 149681990 149681990 CTCCTGCCTCAGCCTCCCCACTAGCTGGGACTACAAGCGCCCGTCAGCACGCTGAGCTAATTTTT CTCCTGCCTCAGCCTCCCCACTAGCTGGGACTGCAAGCGCCCGTCAGCACGCTGAGCTAATTTTT T C LATS1 Ensembl:ENSG00000131023 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1176021174 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_758,RMVar_hsa_circ_125035,RMVar_hsa_circ_358281,RMVar_hsa_circ_242220,RMVar_hsa_circ_90724,RMVar_hsa_circ_242219,RMVar_hsa_circ_369401,RMVar_hsa_circ_270272,RMVar_hsa_circ_242228,RMVar_hsa_circ_242229,RMVar_hsa_circ_377140,RMVar_hsa_circ_10749,RMVar_hsa_circ_67196,RMVar_hsa_circ_265777 28905 RMVar_ID_28905 Human_SNP_ID_301186279 A-to-I Human chr6 - 149693447 149693447 149693447 TGCCACCGTGCCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATCTTGGCCATGC TGCCACCGTGCCCAGCTAATTTTTGTATTTTTTGTAGAGATGGGGTTTCACCATCTTGGCCATGC T A LATS1 Ensembl:ENSG00000131023 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs956057428 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_758,RMVar_hsa_circ_125035,RMVar_hsa_circ_358281,RMVar_hsa_circ_242219,RMVar_hsa_circ_270272,RMVar_hsa_circ_242229,RMVar_hsa_circ_10749,RMVar_hsa_circ_67196,RMVar_hsa_circ_265777,RMVar_hsa_circ_70017,RMVar_hsa_circ_310413 28906 RMVar_ID_28906 Human_SNP_ID_301186794 A-to-I Human chr6 - 149695590 149695590 149695590 TTGCTGCAACATCCACCTCCCAGGTTCAAACAATTCTCATGTCTCAGCCTCCTGAGTAGCTGGAA TTGCTGCAACATCCACCTCCCAGGTTCAAACAGTTCTCATGTCTCAGCCTCCTGAGTAGCTGGAA T C LATS1 Ensembl:ENSG00000131023 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs936777666 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_758,RMVar_hsa_circ_125035,RMVar_hsa_circ_358281,RMVar_hsa_circ_242219,RMVar_hsa_circ_7169,RMVar_hsa_circ_10749,RMVar_hsa_circ_67196,RMVar_hsa_circ_70017,RMVar_hsa_circ_283040,RMVar_hsa_circ_242232 28907 RMVar_ID_28907 Human_SNP_ID_301191709 A-to-I Human chr6 - 149715306 149715306 149715306 CCAGCACTTTGGGAGGCCAAGGAGGGCGGATTACCTGAGGTCTGGAGTTCGAGACCAGCCTGGCC CCAGCACTTTGGGAGGCCAAGGAGGGCGGATTGCCTGAGGTCTGGAGTTCGAGACCAGCCTGGCC T C LATS1 Ensembl:ENSG00000131023 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1029917482 Functional Loss SNV dbSNP153 33..33 33 - - - 28908 RMVar_ID_28908 Human_SNP_ID_301193201 A-to-I Human chr6 - 149720821 149720821 149720821 TTACCCAGGCTGGTCTTGAACTCTTGGGCCCAAGTGATCCTCCTGCCTCAGCCTCCAGAAGTACT TTACCCAGGCTGGTCTTGAACTCTTGGGCCCAGGTGATCCTCCTGCCTCAGCCTCCAGAAGTACT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1046998160 Functional Loss SNV dbSNP153 33..33 33 - - - 28909 RMVar_ID_28909 Human_SNP_ID_301194240 A-to-I Human chr6 - 149724612 149724612 149724612 GCCACTTCACTCCAGCCTGGGCAAAAGAGCAAAACGCCATCTCAAAAAATATACATATATAAGGA GCCACTTCACTCCAGCCTGGGCAAAAGAGCAAGACGCCATCTCAAAAAATATACATATATAAGGA T C NUP43 Ensembl:ENSG00000120253 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-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 28910 RMVar_ID_28910 Human_SNP_ID_301194241 A-to-I Human chr6 - 149724613 149724613 149724613 TGCCACTTCACTCCAGCCTGGGCAAAAGAGCAAAACGCCATCTCAAAAAATATACATATATAAGG TGCCACTTCACTCCAGCCTGGGCAAAAGAGCAGAACGCCATCTCAAAAAATATACATATATAAGG T C NUP43 Ensembl:ENSG00000120253 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048113 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 28911 RMVar_ID_28911 Human_SNP_ID_301194243 A-to-I Human chr6 - 149724619 149724619 149724619 AGATCGTGCCACTTCACTCCAGCCTGGGCAAAAGAGCAAAACGCCATCTCAAAAAATATACATAT AGATCGTGCCACTTCACTCCAGCCTGGGCAAAGGAGCAAAACGCCATCTCAAAAAATATACATAT T C NUP43 Ensembl:ENSG00000120253 Protein coding 3'UTR GSE100210;GSE112787 HepG2 cell line;293 Flip-In T-REx cells,empty vector - 29129909,29967493 RNA-Seq:(High) rs1129806 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 28912 RMVar_ID_28912 Human_SNP_ID_301194250 A-to-I Human chr6 - 149724651 149724651 149724651 CAAACCCGGGAGGCAGAGGTTGCAGTGACCCAAGATCGTGCCACTTCACTCCAGCCTGGGCAAAA CAAACCCGGGAGGCAGAGGTTGCAGTGACCCAGGATCGTGCCACTTCACTCCAGCCTGGGCAAAA T C NUP43 Ensembl:ENSG00000120253 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs767511255 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 28913 RMVar_ID_28913 Human_SNP_ID_301194287 A-to-I Human chr6 - 149724771 149724771 149724771 CAGCCTGGCCAACATGGCGAAACCCCGTCTCCACTAAAAATGCAAAAAAAAAATTAACCGGGCGT CAGCCTGGCCAACATGGCGAAACCCCGTCTCCTCTAAAAATGCAAAAAAAAAATTAACCGGGCGT T A NUP43 Ensembl:ENSG00000120253 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1278582030 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25974327 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 28914 RMVar_ID_28914 Human_SNP_ID_301194291 A-to-I Human chr6 - 149724782 149724782 149724782 GAGTTCGAGATCAGCCTGGCCAACATGGCGAAACCCCGTCTCCACTAAAAATGCAAAAAAAAAAT GAGTTCGAGATCAGCCTGGCCAACATGGCGAAGCCCCGTCTCCACTAAAAATGCAAAAAAAAAAT T C NUP43 Ensembl:ENSG00000120253 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,24183664,29129909,31158229,31158229 RNA-Seq:(High) rs1294252589 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25974327 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 28915 RMVar_ID_28915 Human_SNP_ID_301194294 A-to-I Human chr6 - 149724792 149724792 149724792 CTGAGGTCAAGAGTTCGAGATCAGCCTGGCCAACATGGCGAAACCCCGTCTCCACTAAAAATGCA CTGAGGTCAAGAGTTCGAGATCAGCCTGGCCAGCATGGCGAAACCCCGTCTCCACTAAAAATGCA T C NUP43 Ensembl:ENSG00000120253 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-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 28916 RMVar_ID_28916 Human_SNP_ID_301194301 A-to-I Human chr6 - 149724815 149724815 149724815 GGAGGCCGAGGTGGGTGAAGCACCTGAGGTCAAGAGTTCGAGATCAGCCTGGCCAACATGGCGAA GGAGGCCGAGGTGGGTGAAGCACCTGAGGTCAGGAGTTCGAGATCAGCCTGGCCAACATGGCGAA T C NUP43 Ensembl:ENSG00000120253 Protein coding 3'UTR GSE38233;GSE100210;GSE112787;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;293 Flip-In T-REx cells,empty vector;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,29967493,31158229,31158229,32596459 RNA-Seq:(High) rs1474764756 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 28917 RMVar_ID_28917 Human_SNP_ID_301194312 A-to-I Human chr6 - 149724861 149724860 149724862 ATGGTGGCCAGGCATGGTGGCTCACGCCTGTAATGCTAGCACTTTGGGAGGCCGAGGTGGGTGAA ATGGTGGCCAGGCATGGTGGCTCACGCCTGT__TGCTAGCACTTTGGGAGGCCGAGGTGGGTGAA ATT A NUP43 Ensembl:ENSG00000120253 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1028599110 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_8215787,Human_RBP_ID_17576505,Human_RBP_ID_26533020 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 28918 RMVar_ID_28918 Human_SNP_ID_301194312 A-to-I Human chr6 - 149724862 149724860 149724862 TATGGTGGCCAGGCATGGTGGCTCACGCCTGTAATGCTAGCACTTTGGGAGGCCGAGGTGGGTGA TATGGTGGCCAGGCATGGTGGCTCACGCCTGT__TGCTAGCACTTTGGGAGGCCGAGGTGGGTGA ATT A NUP43 Ensembl:ENSG00000120253 Protein coding 3'UTR GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,29796672,31158229,31158229,31158229 RNA-Seq:(High) rs1028599110 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_8215787,Human_RBP_ID_17576505,Human_RBP_ID_26533020 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 28919 RMVar_ID_28919 Human_SNP_ID_301194313 A-to-I Human chr6 - 149724862 149724862 149724862 TATGGTGGCCAGGCATGGTGGCTCACGCCTGTAATGCTAGCACTTTGGGAGGCCGAGGTGGGTGA TATGGTGGCCAGGCATGGTGGCTCACGCCTGTGATGCTAGCACTTTGGGAGGCCGAGGTGGGTGA T C NUP43 Ensembl:ENSG00000120253 Protein coding 3'UTR GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,29796672,31158229,31158229,31158229 RNA-Seq:(High) rs1425449679 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8215787,Human_RBP_ID_17576505,Human_RBP_ID_26533020 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 28920 RMVar_ID_28920 Human_SNP_ID_301194390 A-to-I Human chr6 - 149725214 149725214 149725214 ACCACAGGTAATCAGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTTAGT ACCACAGGTAATCAGCCCGCCTCGGCCTCCCAGAGTGCTGGGATTACAGGCGTGAGCCACTTAGT T C NUP43 Ensembl:ENSG00000120253 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs113476516 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 28921 RMVar_ID_28921 Human_SNP_ID_301194472 A-to-I Human chr6 - 149725503 149725503 149725503 CTCACTGCAACCTCCGTCTCTTAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGG CTCACTGCAACCTCCGTCTCTTAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGG T C NUP43 Ensembl:ENSG00000120253 Protein coding 3'UTR GSE47997;GSE126723:GSM3611827,GSM3611828,GSM3611829 K562 cells&HepG2 cells;Bronchiolar epithelium,BEP2D cell line - 23474544,31158229 RNA-Seq:(High) rs1020504432 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 28922 RMVar_ID_28922 Human_SNP_ID_301194478 A-to-I Human chr6 - 149725526 149725526 149725526 GGAGTGAAATGGCATGATCTCAGCTCACTGCAACCTCCGTCTCTTAGGTTCAAGCAATTCTCCTG GGAGTGAAATGGCATGATCTCAGCTCACTGCACCCTCCGTCTCTTAGGTTCAAGCAATTCTCCTG T G NUP43 Ensembl:ENSG00000120253 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs371190943 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 28923 RMVar_ID_28923 Human_SNP_ID_301194479 A-to-I Human chr6 - 149725532 149725532 149725532 GAGGCTGGAGTGAAATGGCATGATCTCAGCTCACTGCAACCTCCGTCTCTTAGGTTCAAGCAATT GAGGCTGGAGTGAAATGGCATGATCTCAGCTCGCTGCAACCTCCGTCTCTTAGGTTCAAGCAATT T C NUP43 Ensembl:ENSG00000120253 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251807920 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 28924 RMVar_ID_28924 Human_SNP_ID_301194483 A-to-I Human chr6 - 149725545 149725545 149725545 TGCTCTTGTTGCTGAGGCTGGAGTGAAATGGCATGATCTCAGCTCACTGCAACCTCCGTCTCTTA TGCTCTTGTTGCTGAGGCTGGAGTGAAATGGCGTGATCTCAGCTCACTGCAACCTCCGTCTCTTA T C NUP43 Ensembl:ENSG00000120253 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs976338329 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4868748,Human_RBP_ID_18367204 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 28925 RMVar_ID_28925 Human_SNP_ID_301194496 A-to-I Human chr6 - 149725598 149725598 149725598 AAGGTTTTGCTTTTCTGTCCTAATAAATATATATATTTTTTGAGATGGAGTTTTGCTCTTGTTGC AAGGTTTTGCTTTTCTGTCCTAATAAATATATGTATTTTTTGAGATGGAGTTTTGCTCTTGTTGC T C NUP43 Ensembl:ENSG00000120253 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs58941321 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15683447,Human_RBP_ID_26533038,Human_RBP_ID_26712074 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 28926 RMVar_ID_28926 Human_SNP_ID_301194497 A-to-I Human chr6 - 149725600 149725600 149725600 GTAAGGTTTTGCTTTTCTGTCCTAATAAATATATATATTTTTTGAGATGGAGTTTTGCTCTTGTT GTAAGGTTTTGCTTTTCTGTCCTAATAAATATGTATATTTTTTGAGATGGAGTTTTGCTCTTGTT T C NUP43 Ensembl:ENSG00000120253 Protein coding 3'UTR GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs1184325065 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15683447,Human_RBP_ID_26533038,Human_RBP_ID_26712074 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 28927 RMVar_ID_28927 Human_SNP_ID_301194499 A-to-I Human chr6 - 149725605 149725605 149725605 TTATGGTAAGGTTTTGCTTTTCTGTCCTAATAAATATATATATTTTTTGAGATGGAGTTTTGCTC TTATGGTAAGGTTTTGCTTTTCTGTCCTAATACATATATATATTTTTTGAGATGGAGTTTTGCTC T G NUP43 Ensembl:ENSG00000120253 Protein coding 3'UTR GSE38233;GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,32596459 RNA-Seq:(High) rs990351045 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10264029,Human_RBP_ID_26533038,Human_RBP_ID_26712074 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 28928 RMVar_ID_28928 Human_SNP_ID_301194621 A-to-I Human chr6 - 149726284 149726284 149726284 CTCCTGCCTCAGTCTCCTGAGTAGCTGGAACTACAGGTGTGCGCCACCACGCCCAGCTAATTTTT CTCCTGCCTCAGTCTCCTGAGTAGCTGGAACTGCAGGTGTGCGCCACCACGCCCAGCTAATTTTT T C NUP43 Ensembl:ENSG00000120253 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1276228651 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 28929 RMVar_ID_28929 Human_SNP_ID_301194641 A-to-I Human chr6 - 149726359 149726359 149726359 AGAGTCTTGCTCTGCTGGAGTGCGGTGGTGCAATCTCGGCTCACTGCAACCTCCACCTCCCAGGT AGAGTCTTGCTCTGCTGGAGTGCGGTGGTGCATTCTCGGCTCACTGCAACCTCCACCTCCCAGGT T A NUP43 Ensembl:ENSG00000120253 Protein coding 3'UTR GSE38233;GSE100210;GSE107867;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;ASD brains,cerebellum;ASD brains,temporal_cortex;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,30559470,30559470,31158229 RNA-Seq:(High) rs966585952 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_655308,Human_RBP_ID_7660148,Human_RBP_ID_10264034,Human_RBP_ID_15683478,Human_RBP_ID_27089412 Human_miRNA_ID_686674,Human_miRNA_ID_889246,Human_miRNA_ID_1065853,Human_miRNA_ID_1077180,Human_miRNA_ID_2274958,Human_miRNA_ID_2400845,Human_miRNA_ID_2494780,Human_miRNA_ID_2500705,Human_miRNA_ID_3108739,Human_miRNA_ID_3110180 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 28930 RMVar_ID_28930 Human_SNP_ID_301194642 A-to-I Human chr6 - 149726359 149726359 149726359 AGAGTCTTGCTCTGCTGGAGTGCGGTGGTGCAATCTCGGCTCACTGCAACCTCCACCTCCCAGGT AGAGTCTTGCTCTGCTGGAGTGCGGTGGTGCAGTCTCGGCTCACTGCAACCTCCACCTCCCAGGT T C NUP43 Ensembl:ENSG00000120253 Protein coding 3'UTR GSE38233;GSE100210;GSE107867;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;ASD brains,cerebellum;ASD brains,temporal_cortex;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,30559470,30559470,31158229 RNA-Seq:(High) rs966585952 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_655308,Human_RBP_ID_7660148,Human_RBP_ID_10264034,Human_RBP_ID_15683478,Human_RBP_ID_27089412 Human_miRNA_ID_686674,Human_miRNA_ID_889246,Human_miRNA_ID_1065853,Human_miRNA_ID_1077180,Human_miRNA_ID_2274958,Human_miRNA_ID_2400845,Human_miRNA_ID_2494780,Human_miRNA_ID_2500705,Human_miRNA_ID_3108739,Human_miRNA_ID_3110180 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 28931 RMVar_ID_28931 Human_SNP_ID_301195338 A-to-I Human chr6 - 149729184 149729184 149729184 AGTTCAAGACCAGCCTGGTCCAACATGGTGAAACCCTGTGTCTACTAAAAATACAAAAATTAGCT AGTTCAAGACCAGCCTGGTCCAACATGGTGAAGCCCTGTGTCTACTAAAAATACAAAAATTAGCT T C NUP43 Ensembl:ENSG00000120253 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1022434617 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10264069,Human_RBP_ID_23056128,Human_RBP_ID_26043800 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 28932 RMVar_ID_28932 Human_SNP_ID_301195535 A-to-I Human chr6 - 149730070 149730070 149730070 AGGAGACAGAGGTTTCAGCGAGCCGAGATTGCACCATTGCACTCCAGCCTGGATAGCAAAAGCGA AGGAGACAGAGGTTTCAGCGAGCCGAGATTGCCCCATTGCACTCCAGCCTGGATAGCAAAAGCGA T G NUP43 Ensembl:ENSG00000120253 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1009759016 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 28933 RMVar_ID_28933 Human_SNP_ID_301195537 A-to-I Human chr6 - 149730077 149730077 149730077 TTTACCCAGGAGACAGAGGTTTCAGCGAGCCGAGATTGCACCATTGCACTCCAGCCTGGATAGCA TTTACCCAGGAGACAGAGGTTTCAGCGAGCCGGGATTGCACCATTGCACTCCAGCCTGGATAGCA T C NUP43 Ensembl:ENSG00000120253 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs925275086 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 28934 RMVar_ID_28934 Human_SNP_ID_301195682 A-to-I Human chr6 - 149730790 149730790 149730790 AAGACCAGAGATGCTTGCAACCACAACCAGCTAATTTTTTTTTTTTAATTTTTTTGTAGAGATGA AAGACCAGAGATGCTTGCAACCACAACCAGCTTATTTTTTTTTTTTAATTTTTTTGTAGAGATGA T A NUP43 Ensembl:ENSG00000120253 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs938172584 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15683661 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 28935 RMVar_ID_28935 Human_SNP_ID_301195683 A-to-I Human chr6 - 149730790 149730790 149730790 AAGACCAGAGATGCTTGCAACCACAACCAGCTAATTTTTTTTTTTTAATTTTTTTGTAGAGATGA AAGACCAGAGATGCTTGCAACCACAACCAGCTGATTTTTTTTTTTTAATTTTTTTGTAGAGATGA T C NUP43 Ensembl:ENSG00000120253 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs938172584 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15683661 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 28936 RMVar_ID_28936 Human_SNP_ID_301195711 A-to-I Human chr6 - 149730916 149730916 149730916 TTTTTTTGTTTGAGACAGCGTCTCACTCTGACATGCAGGCTGGACTGCAGTGGCATGATCACAGC TTTTTTTGTTTGAGACAGCGTCTCACTCTGACGTGCAGGCTGGACTGCAGTGGCATGATCACAGC T C NUP43 Ensembl:ENSG00000120253 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs957114023 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15683669,Human_RBP_ID_17576956,Human_RBP_ID_23194570 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 28937 RMVar_ID_28937 Human_SNP_ID_301195751 A-to-I Human chr6 - 149731065 149731065 149731065 TGGGGTTTTGCTATGTTGGCCAGGCTGGTCTCAAACTCCTGGCCTCAAGTGATCTGACCACCTCA TGGGGTTTTGCTATGTTGGCCAGGCTGGTCTCGAACTCCTGGCCTCAAGTGATCTGACCACCTCA T C NUP43 Ensembl:ENSG00000120253 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1191898600 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 28938 RMVar_ID_28938 Human_SNP_ID_301195804 A-to-I Human chr6 - 149731303 149731303 149731303 CGCCTGCCTCAGCCTCCCAAAGTGCTGAGATTACAGGAGTGAGCCACCACACCTGGCCTTTTTTT CGCCTGCCTCAGCCTCCCAAAGTGCTGAGATTGCAGGAGTGAGCCACCACACCTGGCCTTTTTTT T C NUP43 Ensembl:ENSG00000120253 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs991029397 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 28939 RMVar_ID_28939 Human_SNP_ID_301195822 A-to-I Human chr6 - 149731377 149731377 149731377 TTTTGTATTTTTAGTGGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCT TTTTGTATTTTTAGTGGAGATGGGGTTTCACCGTGTTGGCCAGGCTGGTCTCGAACTCCTGACCT T C NUP43 Ensembl:ENSG00000120253 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1348230409 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 28940 RMVar_ID_28940 Human_SNP_ID_301195855 A-to-I Human chr6 - 149731511 149731511 149731511 TCACCCAGGCTGGAATGCAGTGGCACGATCTCAGCTCACTGCAACCTCCGCCTCCTGGGTTCAAG TCACCCAGGCTGGAATGCAGTGGCACGATCTCGGCTCACTGCAACCTCCGCCTCCTGGGTTCAAG T C NUP43 Ensembl:ENSG00000120253 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1248327563 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 28941 RMVar_ID_28941 Human_SNP_ID_301197513 A-to-I Human chr6 - 149737476 149737476 149737476 GGTGAGAAGTTTGAGACCAGCTAGGGCAACACAGTGAGACCCCATCTCTACCAAAATTTCTTAAA GGTGAGAAGTTTGAGACCAGCTAGGGCAACACGGTGAGACCCCATCTCTACCAAAATTTCTTAAA T C NUP43 Ensembl:ENSG00000120253 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1386392787 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15683851 RMVar_hsa_circ_104444,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_23535,RMVar_hsa_circ_15139,RMVar_hsa_circ_118549,RMVar_hsa_circ_345841,RMVar_hsa_circ_364751,RMVar_hsa_circ_96760,RMVar_hsa_circ_242242,RMVar_hsa_circ_242244,RMVar_hsa_circ_242243,RMVar_hsa_circ_94023,RMVar_hsa_circ_304706,RMVar_hsa_circ_242246 28942 RMVar_ID_28942 Human_SNP_ID_301209389 A-to-I Human chr6 + 149778722 149778722 149778722 ACCACCCTTTACTTTTTAAAAACATTTTCTGTAGAGATGAGGACTCACTGTGTTGCCCAAGCTAG ACCACCCTTTACTTTTTAAAAACATTTTCTGTGGAGATGAGGACTCACTGTGTTGCCCAAGCTAG A G PCMT1 Ensembl:ENSG00000120265 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928975849 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15684623 RMVar_hsa_circ_119973,RMVar_hsa_circ_242252,RMVar_hsa_circ_242250,RMVar_hsa_circ_242253,RMVar_hsa_circ_242251,RMVar_hsa_circ_37424,RMVar_hsa_circ_242259,RMVar_hsa_circ_104512,RMVar_hsa_circ_294390,RMVar_hsa_circ_305365,RMVar_hsa_circ_305192,RMVar_hsa_circ_280571,RMVar_hsa_circ_292334,RMVar_hsa_circ_88233,RMVar_hsa_circ_242260,RMVar_hsa_circ_242255,RMVar_hsa_circ_242257,RMVar_hsa_circ_242258,RMVar_hsa_circ_242256,RMVar_hsa_circ_91931,RMVar_hsa_circ_242254,RMVar_hsa_circ_81725,RMVar_hsa_circ_242264,RMVar_hsa_circ_242265 28943 RMVar_ID_28943 Human_SNP_ID_301209390 A-to-I Human chr6 + 149778722 149778722 149778722 ACCACCCTTTACTTTTTAAAAACATTTTCTGTAGAGATGAGGACTCACTGTGTTGCCCAAGCTAG ACCACCCTTTACTTTTTAAAAACATTTTCTGTTGAGATGAGGACTCACTGTGTTGCCCAAGCTAG A T PCMT1 Ensembl:ENSG00000120265 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928975849 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15684623 RMVar_hsa_circ_119973,RMVar_hsa_circ_242252,RMVar_hsa_circ_242250,RMVar_hsa_circ_242253,RMVar_hsa_circ_242251,RMVar_hsa_circ_37424,RMVar_hsa_circ_242259,RMVar_hsa_circ_104512,RMVar_hsa_circ_294390,RMVar_hsa_circ_305365,RMVar_hsa_circ_305192,RMVar_hsa_circ_280571,RMVar_hsa_circ_292334,RMVar_hsa_circ_88233,RMVar_hsa_circ_242260,RMVar_hsa_circ_242255,RMVar_hsa_circ_242257,RMVar_hsa_circ_242258,RMVar_hsa_circ_242256,RMVar_hsa_circ_91931,RMVar_hsa_circ_242254,RMVar_hsa_circ_81725,RMVar_hsa_circ_242264,RMVar_hsa_circ_242265 28944 RMVar_ID_28944 Human_SNP_ID_301209393 A-to-I Human chr6 + 149778748 149778748 149778748 TTCTGTAGAGATGAGGACTCACTGTGTTGCCCAAGCTAGTTCTGAACCCTGGAGCTCAAGCGATC TTCTGTAGAGATGAGGACTCACTGTGTTGCCCCAGCTAGTTCTGAACCCTGGAGCTCAAGCGATC A C PCMT1 Ensembl:ENSG00000120265 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1019239336 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7558711,Human_RBP_ID_15684623 RMVar_hsa_circ_119973,RMVar_hsa_circ_242252,RMVar_hsa_circ_242250,RMVar_hsa_circ_242253,RMVar_hsa_circ_242251,RMVar_hsa_circ_37424,RMVar_hsa_circ_242259,RMVar_hsa_circ_104512,RMVar_hsa_circ_294390,RMVar_hsa_circ_305365,RMVar_hsa_circ_305192,RMVar_hsa_circ_280571,RMVar_hsa_circ_292334,RMVar_hsa_circ_88233,RMVar_hsa_circ_242260,RMVar_hsa_circ_242255,RMVar_hsa_circ_242257,RMVar_hsa_circ_242258,RMVar_hsa_circ_242256,RMVar_hsa_circ_91931,RMVar_hsa_circ_242254,RMVar_hsa_circ_81725,RMVar_hsa_circ_242264,RMVar_hsa_circ_242265 28945 RMVar_ID_28945 Human_SNP_ID_301209394 A-to-I Human chr6 + 149778748 149778748 149778748 TTCTGTAGAGATGAGGACTCACTGTGTTGCCCAAGCTAGTTCTGAACCCTGGAGCTCAAGCGATC TTCTGTAGAGATGAGGACTCACTGTGTTGCCCGAGCTAGTTCTGAACCCTGGAGCTCAAGCGATC A G PCMT1 Ensembl:ENSG00000120265 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1019239336 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7558711,Human_RBP_ID_15684623 RMVar_hsa_circ_119973,RMVar_hsa_circ_242252,RMVar_hsa_circ_242250,RMVar_hsa_circ_242253,RMVar_hsa_circ_242251,RMVar_hsa_circ_37424,RMVar_hsa_circ_242259,RMVar_hsa_circ_104512,RMVar_hsa_circ_294390,RMVar_hsa_circ_305365,RMVar_hsa_circ_305192,RMVar_hsa_circ_280571,RMVar_hsa_circ_292334,RMVar_hsa_circ_88233,RMVar_hsa_circ_242260,RMVar_hsa_circ_242255,RMVar_hsa_circ_242257,RMVar_hsa_circ_242258,RMVar_hsa_circ_242256,RMVar_hsa_circ_91931,RMVar_hsa_circ_242254,RMVar_hsa_circ_81725,RMVar_hsa_circ_242264,RMVar_hsa_circ_242265 28946 RMVar_ID_28946 Human_SNP_ID_301216407 A-to-I Human chr6 + 149804770 149804770 149804770 GTGATCTGCCCGCCTCGGCCTCCCAAAGTGCTAGGATTACAGGTGTCAGCCACCATGCCTGGCCC GTGATCTGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTCAGCCACCATGCCTGGCCC A G PCMT1 Ensembl:ENSG00000120265 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs929455489 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88233,RMVar_hsa_circ_91931,RMVar_hsa_circ_242254,RMVar_hsa_circ_82745,RMVar_hsa_circ_242265,RMVar_hsa_circ_242269 28947 RMVar_ID_28947 Human_SNP_ID_301220284 A-to-I Human chr6 - 149820946 149820946 149820946 AGCCTGGGCAACAGAGCAAGACTCCATCTCAAAAAAAAAAAAAAAAAAAAGTCTAGGTTTGGGAC AGCCTGGGCAACAGAGCAAGACTCCATCTCAACAAAAAAAAAAAAAAAAAGTCTAGGTTTGGGAC T G AL355312.6,AL355312.5,LRP11 Ensembl:ENSG00000285991,Ensembl:ENSG00000285889,Ensembl:ENSG00000120256 Protein coding,lincRNA,Protein coding intron,intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1422026427 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265411 28948 RMVar_ID_28948 Human_SNP_ID_301220343 A-to-I Human chr6 - 149821196 149821196 149821196 GGCCGGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGTGGATCACG GGCCGGGCACGGTGGCTCACGCCTGTAATCCCGGCACTTTGGGAGGCCGAGGCAGGTGGATCACG T C AL355312.6,AL355312.5,LRP11 Ensembl:ENSG00000285991,Ensembl:ENSG00000285889,Ensembl:ENSG00000120256 Protein coding,lincRNA,Protein coding intron,intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs188363724 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265411 28949 RMVar_ID_28949 Human_SNP_ID_301220524 A-to-I Human chr6 - 149822175 149822175 149822175 CCACAACTGGCTAATAATTTTTTGTAGAGACAAGGTCTCGCCATGTTGCCCAGGCTGGTCTCGAA CCACAACTGGCTAATAATTTTTTGTAGAGACAGGGTCTCGCCATGTTGCCCAGGCTGGTCTCGAA T C AL355312.6,AL355312.5,LRP11 Ensembl:ENSG00000285991,Ensembl:ENSG00000285889,Ensembl:ENSG00000120256 Protein coding,lincRNA,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs897150196 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265411 28950 RMVar_ID_28950 Human_SNP_ID_301220580 A-to-I Human chr6 - 149822446 149822445 149822446 CCAAGCTGGAGTACAGTTTAAGAGCTCACTGAAGCCTCTACCTCCCAGACTCAAGTGATCCTTCT CCAAGCTGGAGTACAGTTTAAGAGCTCACTGA_GCCTCTACCTCCCAGACTCAAGTGATCCTTCT CT C AL355312.6,AL355312.5,LRP11 Ensembl:ENSG00000285991,Ensembl:ENSG00000285889,Ensembl:ENSG00000120256 Protein coding,lincRNA,Protein coding intron,intron,intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1291807673 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_24388586 RMVar_hsa_circ_265411 28951 RMVar_ID_28951 Human_SNP_ID_301221076 A-to-I Human chr6 - 149824824 149824823 149824824 ATCGAGTCTCACTCTGTTGTCCAGGTTGGAGTACAGCGGCGCGATCTCAGCTCACTGCAGCCTCT ATCGAGTCTCACTCTGTTGTCCAGGTTGGAGT_CAGCGGCGCGATCTCAGCTCACTGCAGCCTCT GT G AL355312.6,AL355312.5,LRP11 Ensembl:ENSG00000285991,Ensembl:ENSG00000285889,Ensembl:ENSG00000120256 Protein coding,lincRNA,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1562435659 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_265411 28952 RMVar_ID_28952 Human_SNP_ID_301221263 A-to-I Human chr6 - 149825708 149825708 149825708 GAGGCTGCAGTGAGATAAGATTGTGCCACTGCACTCCAGCCTGGGTGACAGAGTGAGACCGTCTC GAGGCTGCAGTGAGATAAGATTGTGCCACTGCTCTCCAGCCTGGGTGACAGAGTGAGACCGTCTC T A AL355312.6,AL355312.5,LRP11 Ensembl:ENSG00000285991,Ensembl:ENSG00000285889,Ensembl:ENSG00000120256 Protein coding,lincRNA,Protein coding intron,intron,intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs549483778 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78750,RMVar_hsa_circ_265411,RMVar_hsa_circ_98949,RMVar_hsa_circ_242271,RMVar_hsa_circ_242272 28953 RMVar_ID_28953 Human_SNP_ID_301221287 A-to-I Human chr6 - 149825822 149825822 149825822 CAATATGGCAAAATCCTGTCTCTACAAAAAATACAAAAATTAGCCAAGTGTGGTGACATTCGCCT CAATATGGCAAAATCCTGTCTCTACAAAAAATTCAAAAATTAGCCAAGTGTGGTGACATTCGCCT T A AL355312.6,AL355312.5,LRP11 Ensembl:ENSG00000285991,Ensembl:ENSG00000285889,Ensembl:ENSG00000120256 Protein coding,lincRNA,Protein coding intron,intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs914106410 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78750,RMVar_hsa_circ_265411,RMVar_hsa_circ_98949,RMVar_hsa_circ_242271,RMVar_hsa_circ_242272 28954 RMVar_ID_28954 Human_SNP_ID_301221288 A-to-I Human chr6 - 149825828 149825828 149825828 CCTGGGCAATATGGCAAAATCCTGTCTCTACAAAAAATACAAAAATTAGCCAAGTGTGGTGACAT CCTGGGCAATATGGCAAAATCCTGTCTCTACAGAAAATACAAAAATTAGCCAAGTGTGGTGACAT T C AL355312.6,AL355312.5,LRP11 Ensembl:ENSG00000285991,Ensembl:ENSG00000285889,Ensembl:ENSG00000120256 Protein coding,lincRNA,Protein coding intron,intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs192190288 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78750,RMVar_hsa_circ_265411,RMVar_hsa_circ_98949,RMVar_hsa_circ_242271,RMVar_hsa_circ_242272 28955 RMVar_ID_28955 Human_SNP_ID_301221289 A-to-I Human chr6 - 149825829 149825829 149825829 GCCTGGGCAATATGGCAAAATCCTGTCTCTACAAAAAATACAAAAATTAGCCAAGTGTGGTGACA GCCTGGGCAATATGGCAAAATCCTGTCTCTACCAAAAATACAAAAATTAGCCAAGTGTGGTGACA T G AL355312.6,AL355312.5,LRP11 Ensembl:ENSG00000285991,Ensembl:ENSG00000285889,Ensembl:ENSG00000120256 Protein coding,lincRNA,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982251727 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78750,RMVar_hsa_circ_265411,RMVar_hsa_circ_98949,RMVar_hsa_circ_242271,RMVar_hsa_circ_242272 28956 RMVar_ID_28956 Human_SNP_ID_301221311 A-to-I Human chr6 - 149825938 149825938 149825938 CACAATTCAAATCCTTGCTCAAAGCTGGGCACAGTGGCTCACGCCTGTAATCCCAGCACTTTGGG CACAATTCAAATCCTTGCTCAAAGCTGGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG T C AL355312.6,AL355312.5,LRP11 Ensembl:ENSG00000285991,Ensembl:ENSG00000285889,Ensembl:ENSG00000120256 Protein coding,lincRNA,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1468672231 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78750,RMVar_hsa_circ_265411,RMVar_hsa_circ_98949,RMVar_hsa_circ_242271,RMVar_hsa_circ_242272 28957 RMVar_ID_28957 Human_SNP_ID_301234237 A-to-I Human chr6 - 149880387 149880387 149880387 TTCCTCTACTCCACTTTATCTGCCTTCTTCACAGTCACAGCAATCTCTTTGATCGTGTTAACTAC TTCCTCTACTCCACTTTATCTGCCTTCTTCACGGTCACAGCAATCTCTTTGATCGTGTTAACTAC T C AL355312.6 Ensembl:ENSG00000285991 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1393020801 Functional Loss SNV dbSNP153 33..33 33 - - - 28958 RMVar_ID_28958 Human_SNP_ID_301234247 A-to-I Human chr6 - 149880412 149880412 149880412 GGTCCTGGCACACTACTCCAGCAGCTTCCTCTACTCCACTTTATCTGCCTTCTTCACAGTCACAG GGTCCTGGCACACTACTCCAGCAGCTTCCTCTGCTCCACTTTATCTGCCTTCTTCACAGTCACAG T C AL355312.6 Ensembl:ENSG00000285991 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1376889314 Functional Loss SNV dbSNP153 33..33 33 - - - 28959 RMVar_ID_28959 Human_SNP_ID_301234360 A-to-I Human chr6 + 149880896 149880896 149880896 ACATGTTCTGTGCTGGCCAAGTACCTGAGGAGAATCTGAAGAGGACAATGATGGCCTGTGGAGGC ACATGTTCTGTGCTGGCCAAGTACCTGAGGAGGATCTGAAGAGGACAATGATGGCCTGTGGAGGC A G AL355312.3,CCT7P1 Ensembl:ENSG00000268592,Ensembl:ENSG00000217733 lincRNA,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878936562 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1678888,Human_RBP_ID_2011370,Human_RBP_ID_5216128,Human_RBP_ID_8270461,Human_RBP_ID_8634206,Human_RBP_ID_15685336,Human_RBP_ID_18856444,Human_RBP_ID_26533127 Human_miRNA_ID_1844380,Human_miRNA_ID_1869773,Human_miRNA_ID_1906564 28960 RMVar_ID_28960 Human_SNP_ID_301234374 A-to-I Human chr6 + 149880944 149880944 149880944 TGATGGCCTGTGGAGGCTCAATCCAGACCAGTACGAATGCTTTCTTAGCAGATGTGCTGGGTCGA TGATGGCCTGTGGAGGCTCAATCCAGACCAGTGCGAATGCTTTCTTAGCAGATGTGCTGGGTCGA A G AL355312.3,CCT7P1 Ensembl:ENSG00000268592,Ensembl:ENSG00000217733 lincRNA,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1466778021 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1818630 28961 RMVar_ID_28961 Human_SNP_ID_361961573 A-to-I Human chr8 + 47340333 47340333 47340333 ACACGTACAATAAACGTGAATAGGCCAGGTGCAGTGGCTCATGCTTGTAATCCCAGCACTTTGGG ACACGTACAATAAACGTGAATAGGCCAGGTGCCGTGGCTCATGCTTGTAATCCCAGCACTTTGGG A C SPIDR Ensembl:ENSG00000164808 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs547457660 Functional Loss SNV dbSNP153 33..33 33 - - - 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_62175,RMVar_hsa_circ_33506,RMVar_hsa_circ_40623,RMVar_hsa_circ_357413,RMVar_hsa_circ_334257,RMVar_hsa_circ_343221,RMVar_hsa_circ_331439 28962 RMVar_ID_28962 Human_SNP_ID_361961624 A-to-I Human chr8 + 47340495 47340495 47340495 GACATGGTGGCACCCTGTAGTCTCAGCTACTCAGGAGTCTGAGGTGGGAGAATCACTTGAACCCA GACATGGTGGCACCCTGTAGTCTCAGCTACTCGGGAGTCTGAGGTGGGAGAATCACTTGAACCCA A G SPIDR Ensembl:ENSG00000164808 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1156437017 Functional Loss SNV dbSNP153 33..33 33 - - - 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_62175,RMVar_hsa_circ_33506,RMVar_hsa_circ_40623,RMVar_hsa_circ_357413,RMVar_hsa_circ_334257,RMVar_hsa_circ_343221,RMVar_hsa_circ_331439 28963 RMVar_ID_28963 Human_SNP_ID_362007337 A-to-I Human chr8 + 47511920 47511920 47511920 TCATCCTCATCTTGGTCATGAGTGAGATCTCTAAAGGATGTCACTCTATTATCACTAGGGGCTGT TCATCCTCATCTTGGTCATGAGTGAGATCTCTGAAGGATGTCACTCTATTATCACTAGGGGCTGT A G SPIDR Ensembl:ENSG00000164808 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1405028460 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13332,RMVar_hsa_circ_349030,RMVar_hsa_circ_61259,RMVar_hsa_circ_37491,RMVar_hsa_circ_316687,RMVar_hsa_circ_325555,RMVar_hsa_circ_40623,RMVar_hsa_circ_73193,RMVar_hsa_circ_368502,RMVar_hsa_circ_65895,RMVar_hsa_circ_21499,RMVar_hsa_circ_85118,RMVar_hsa_circ_88821,RMVar_hsa_circ_251777,RMVar_hsa_circ_25170,RMVar_hsa_circ_251778,RMVar_hsa_circ_47158 28964 RMVar_ID_28964 Human_SNP_ID_362007348 A-to-I Human chr8 + 47511944 47511944 47511944 AGATCTCTAAAGGATGTCACTCTATTATCACTAGGGGCTGTGCCTCTGGACACTGAACTGGGGGT AGATCTCTAAAGGATGTCACTCTATTATCACTGGGGGCTGTGCCTCTGGACACTGAACTGGGGGT A G SPIDR Ensembl:ENSG00000164808 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1200468397 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13332,RMVar_hsa_circ_349030,RMVar_hsa_circ_61259,RMVar_hsa_circ_37491,RMVar_hsa_circ_316687,RMVar_hsa_circ_325555,RMVar_hsa_circ_40623,RMVar_hsa_circ_73193,RMVar_hsa_circ_368502,RMVar_hsa_circ_65895,RMVar_hsa_circ_21499,RMVar_hsa_circ_85118,RMVar_hsa_circ_88821,RMVar_hsa_circ_251777,RMVar_hsa_circ_25170,RMVar_hsa_circ_251778,RMVar_hsa_circ_47158 28965 RMVar_ID_28965 Human_SNP_ID_362009801 A-to-I Human chr8 + 47522096 47522096 47522096 TGAGGCAGGAGAATCGCTTGAACCTGAGAGACAGAGATTGCAGTGAGCCGAGATCGTGCCACTGT TGAGGCAGGAGAATCGCTTGAACCTGAGAGACGGAGATTGCAGTGAGCCGAGATCGTGCCACTGT A G SPIDR Ensembl:ENSG00000164808 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1439193741 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13332,RMVar_hsa_circ_349030,RMVar_hsa_circ_61259,RMVar_hsa_circ_37491,RMVar_hsa_circ_316687,RMVar_hsa_circ_325555,RMVar_hsa_circ_40623,RMVar_hsa_circ_73193,RMVar_hsa_circ_368502,RMVar_hsa_circ_65895,RMVar_hsa_circ_21499,RMVar_hsa_circ_85118,RMVar_hsa_circ_88821,RMVar_hsa_circ_251777,RMVar_hsa_circ_25170,RMVar_hsa_circ_251778,RMVar_hsa_circ_47158 28966 RMVar_ID_28966 Human_SNP_ID_362010050 A-to-I Human chr8 + 47523054 47523054 47523054 CGAGGGTCTCACCCTGTCCCCCAGGCTGGAGTACAGTGTCACAATCTCAGCTCACTGCAGCCTCG CGAGGGTCTCACCCTGTCCCCCAGGCTGGAGTGCAGTGTCACAATCTCAGCTCACTGCAGCCTCG A G SPIDR Ensembl:ENSG00000164808 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1030690368 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13332,RMVar_hsa_circ_349030,RMVar_hsa_circ_61259,RMVar_hsa_circ_37491,RMVar_hsa_circ_316687,RMVar_hsa_circ_325555,RMVar_hsa_circ_40623,RMVar_hsa_circ_73193,RMVar_hsa_circ_368502,RMVar_hsa_circ_65895,RMVar_hsa_circ_21499,RMVar_hsa_circ_85118,RMVar_hsa_circ_88821,RMVar_hsa_circ_251777,RMVar_hsa_circ_25170,RMVar_hsa_circ_251778,RMVar_hsa_circ_47158 28967 RMVar_ID_28967 Human_SNP_ID_362010635 A-to-I Human chr8 + 47525639 47525613 47525639 CCTGGCCAACATGGTGAAACCCCATCTCTACCAAAAATACAAAAATTAGCCAGACGTGGTGGCAT CCTGGCC__________________________AAAATACAAAAATTAGCCAGACGTGGTGGCAT CAACATGGTGAAACCCCATCTCTACCA C SPIDR Ensembl:ENSG00000164808 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1309842505 Functional Loss DEL dbSNP153 8..33 33 - - - RMVar_hsa_circ_13332,RMVar_hsa_circ_349030,RMVar_hsa_circ_61259,RMVar_hsa_circ_37491,RMVar_hsa_circ_316687,RMVar_hsa_circ_325555,RMVar_hsa_circ_40623,RMVar_hsa_circ_73193,RMVar_hsa_circ_368502,RMVar_hsa_circ_65895,RMVar_hsa_circ_21499,RMVar_hsa_circ_85118,RMVar_hsa_circ_88821,RMVar_hsa_circ_251777,RMVar_hsa_circ_25170,RMVar_hsa_circ_251778,RMVar_hsa_circ_47158 28968 RMVar_ID_28968 Human_SNP_ID_362010639 A-to-I Human chr8 + 47525639 47525638 47525639 CCTGGCCAACATGGTGAAACCCCATCTCTACCAAAAATACAAAAATTAGCCAGACGTGGTGGCAT CCTGGCCAACATGGTGAAACCCCATCTCTACC_AAAATACAAAAATTAGCCAGACGTGGTGGCAT CA C SPIDR Ensembl:ENSG00000164808 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1353149774 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_13332,RMVar_hsa_circ_349030,RMVar_hsa_circ_61259,RMVar_hsa_circ_37491,RMVar_hsa_circ_316687,RMVar_hsa_circ_325555,RMVar_hsa_circ_40623,RMVar_hsa_circ_73193,RMVar_hsa_circ_368502,RMVar_hsa_circ_65895,RMVar_hsa_circ_21499,RMVar_hsa_circ_85118,RMVar_hsa_circ_88821,RMVar_hsa_circ_251777,RMVar_hsa_circ_25170,RMVar_hsa_circ_251778,RMVar_hsa_circ_47158 28969 RMVar_ID_28969 Human_SNP_ID_362027668 A-to-I Human chr8 - 47592174 47592174 47592174 AAAGCCCAAGCCATAGAAACAGCTAGAGCATGAACTAGGCTATATGCCATGAATAATATTTAAAT AAAGCCCAAGCCATAGAAACAGCTAGAGCATGGACTAGGCTATATGCCATGAATAATATTTAAAT T C AC024451.3 Ensembl:ENSG00000254065 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1488114464 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7840343 28970 RMVar_ID_28970 Human_SNP_ID_362060801 A-to-I Human chr8 + 47730600 47730600 47730600 CCATGGCCAGATTCTAGCCAGAATTTTTTTTTAGGCAGAGTCTTACTCTGTCATCCAGGCTGGAG CCATGGCCAGATTCTAGCCAGAATTTTTTTTTTGGCAGAGTCTTACTCTGTCATCCAGGCTGGAG A T SPIDR Ensembl:ENSG00000164808 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs1382474644 Functional Loss SNV dbSNP153 33..33 33 - - - 28971 RMVar_ID_28971 Human_SNP_ID_362060804 A-to-I Human chr8 + 47730612 47730612 47730612 TCTAGCCAGAATTTTTTTTTAGGCAGAGTCTTACTCTGTCATCCAGGCTGGAGTGCAGTGACACA TCTAGCCAGAATTTTTTTTTAGGCAGAGTCTTCCTCTGTCATCCAGGCTGGAGTGCAGTGACACA A C SPIDR Ensembl:ENSG00000164808 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs533720493 Functional Loss SNV dbSNP153 33..33 33 - - - 28972 RMVar_ID_28972 Human_SNP_ID_362060821 A-to-I Human chr8 + 47730686 47730686 47730686 TCACTACAGCCTCGAACTCCTGGGCTCAAACGATCCCCCTGCCTCAGCCTCCCAAGTATCCAACC TCACTACAGCCTCGAACTCCTGGGCTCAAACGTTCCCCCTGCCTCAGCCTCCCAAGTATCCAACC A T SPIDR Ensembl:ENSG00000164808 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215537710 Functional Loss SNV dbSNP153 33..33 33 - - - 28973 RMVar_ID_28973 Human_SNP_ID_362060947 A-to-I Human chr8 + 47731197 47731197 47731197 AGAATCACTGGAACTGGGGAGGTAGAGGTTGCAGTGAGCTGAGATTGTGCCATACTCCAGCCTGG AGAATCACTGGAACTGGGGAGGTAGAGGTTGCCGTGAGCTGAGATTGTGCCATACTCCAGCCTGG A C SPIDR Ensembl:ENSG00000164808 Protein coding intron GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs1267970441 Functional Loss SNV dbSNP153 33..33 33 - - - 28974 RMVar_ID_28974 Human_SNP_ID_362073033 A-to-I Human chr8 - 47775179 47775179 47775179 TTTATTTATTTATTTATTTATTTTTGAGACAAAGTCTTGCTCTGTCACCCAGGCTGGAGTGCAAT TTTATTTATTTATTTATTTATTTTTGAGACAAGGTCTTGCTCTGTCACCCAGGCTGGAGTGCAAT T C PRKDC Ensembl:ENSG00000253729 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs921818615 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110783,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_117587,RMVar_hsa_circ_110848,RMVar_hsa_circ_251807,RMVar_hsa_circ_99346,RMVar_hsa_circ_105975,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_89044,RMVar_hsa_circ_93636,RMVar_hsa_circ_95042,RMVar_hsa_circ_92986,RMVar_hsa_circ_251811,RMVar_hsa_circ_251815,RMVar_hsa_circ_84002,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_251799,RMVar_hsa_circ_251803,RMVar_hsa_circ_251805,RMVar_hsa_circ_251806,RMVar_hsa_circ_251804,RMVar_hsa_circ_251801,RMVar_hsa_circ_251802,RMVar_hsa_circ_251800,RMVar_hsa_circ_251795,RMVar_hsa_circ_251797,RMVar_hsa_circ_251798,RMVar_hsa_circ_251796,RMVar_hsa_circ_251793,RMVar_hsa_circ_251794 28975 RMVar_ID_28975 Human_SNP_ID_362073034 A-to-I Human chr8 - 47775179 47775179 47775179 TTTATTTATTTATTTATTTATTTTTGAGACAAAGTCTTGCTCTGTCACCCAGGCTGGAGTGCAAT TTTATTTATTTATTTATTTATTTTTGAGACAACGTCTTGCTCTGTCACCCAGGCTGGAGTGCAAT T G PRKDC Ensembl:ENSG00000253729 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs921818615 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110783,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_117587,RMVar_hsa_circ_110848,RMVar_hsa_circ_251807,RMVar_hsa_circ_99346,RMVar_hsa_circ_105975,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_89044,RMVar_hsa_circ_93636,RMVar_hsa_circ_95042,RMVar_hsa_circ_92986,RMVar_hsa_circ_251811,RMVar_hsa_circ_251815,RMVar_hsa_circ_84002,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_251799,RMVar_hsa_circ_251803,RMVar_hsa_circ_251805,RMVar_hsa_circ_251806,RMVar_hsa_circ_251804,RMVar_hsa_circ_251801,RMVar_hsa_circ_251802,RMVar_hsa_circ_251800,RMVar_hsa_circ_251795,RMVar_hsa_circ_251797,RMVar_hsa_circ_251798,RMVar_hsa_circ_251796,RMVar_hsa_circ_251793,RMVar_hsa_circ_251794 28976 RMVar_ID_28976 Human_SNP_ID_362074315 A-to-I Human chr8 - 47779772 47779772 47779772 CAGCCTGGCCAACGTGGTGAAACCCCGTCTCTACTAAAAATACAGAAATTAGCTGAGCATGGTGG CAGCCTGGCCAACGTGGTGAAACCCCGTCTCTTCTAAAAATACAGAAATTAGCTGAGCATGGTGG T A PRKDC Ensembl:ENSG00000253729 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1206523640 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110783,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_117587,RMVar_hsa_circ_110848,RMVar_hsa_circ_251807,RMVar_hsa_circ_99346,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_93636,RMVar_hsa_circ_95042,RMVar_hsa_circ_92986,RMVar_hsa_circ_251811,RMVar_hsa_circ_251815,RMVar_hsa_circ_84002,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_251803,RMVar_hsa_circ_251805,RMVar_hsa_circ_251806,RMVar_hsa_circ_251804,RMVar_hsa_circ_251801,RMVar_hsa_circ_251802,RMVar_hsa_circ_251800,RMVar_hsa_circ_251795,RMVar_hsa_circ_251797,RMVar_hsa_circ_251796,RMVar_hsa_circ_251793,RMVar_hsa_circ_251794,RMVar_hsa_circ_348054,RMVar_hsa_circ_370434,RMVar_hsa_circ_329249,RMVar_hsa_circ_61996,RMVar_hsa_circ_90465,RMVar_hsa_circ_12997,RMVar_hsa_circ_15990,RMVar_hsa_circ_265144,RMVar_hsa_circ_251818,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_370118,RMVar_hsa_circ_76511,RMVar_hsa_circ_251824,RMVar_hsa_circ_251825,RMVar_hsa_circ_251823 28977 RMVar_ID_28977 Human_SNP_ID_362074437 A-to-I Human chr8 - 47780090 47780090 47780090 GTCAACATGGCAAAACCCTGTCTCTACTGAAAATAGAAAAATTAGCTGGGTGTAGTGGCGGGCGC GTCAACATGGCAAAACCCTGTCTCTACTGAAAGTAGAAAAATTAGCTGGGTGTAGTGGCGGGCGC T C PRKDC Ensembl:ENSG00000253729 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1329901533 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10397900,Human_RBP_ID_23086229,Human_RBP_ID_26192864 RMVar_hsa_circ_110783,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_117587,RMVar_hsa_circ_110848,RMVar_hsa_circ_251807,RMVar_hsa_circ_99346,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_93636,RMVar_hsa_circ_95042,RMVar_hsa_circ_92986,RMVar_hsa_circ_251811,RMVar_hsa_circ_251815,RMVar_hsa_circ_84002,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_251803,RMVar_hsa_circ_251805,RMVar_hsa_circ_251806,RMVar_hsa_circ_251804,RMVar_hsa_circ_251801,RMVar_hsa_circ_251802,RMVar_hsa_circ_251800,RMVar_hsa_circ_251795,RMVar_hsa_circ_251797,RMVar_hsa_circ_251796,RMVar_hsa_circ_251793,RMVar_hsa_circ_251794,RMVar_hsa_circ_348054,RMVar_hsa_circ_370434,RMVar_hsa_circ_329249,RMVar_hsa_circ_61996,RMVar_hsa_circ_90465,RMVar_hsa_circ_12997,RMVar_hsa_circ_15990,RMVar_hsa_circ_265144,RMVar_hsa_circ_251818,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_370118,RMVar_hsa_circ_76511,RMVar_hsa_circ_251824,RMVar_hsa_circ_251825,RMVar_hsa_circ_251823 28978 RMVar_ID_28978 Human_SNP_ID_362074438 A-to-I Human chr8 - 47780097 47780097 47780097 CAGTCTGGTCAACATGGCAAAACCCTGTCTCTACTGAAAATAGAAAAATTAGCTGGGTGTAGTGG CAGTCTGGTCAACATGGCAAAACCCTGTCTCTGCTGAAAATAGAAAAATTAGCTGGGTGTAGTGG T C PRKDC Ensembl:ENSG00000253729 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs955837496 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10397900,Human_RBP_ID_23086229,Human_RBP_ID_26192864 RMVar_hsa_circ_110783,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_117587,RMVar_hsa_circ_110848,RMVar_hsa_circ_251807,RMVar_hsa_circ_99346,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_93636,RMVar_hsa_circ_95042,RMVar_hsa_circ_92986,RMVar_hsa_circ_251811,RMVar_hsa_circ_251815,RMVar_hsa_circ_84002,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_251803,RMVar_hsa_circ_251805,RMVar_hsa_circ_251806,RMVar_hsa_circ_251804,RMVar_hsa_circ_251801,RMVar_hsa_circ_251802,RMVar_hsa_circ_251800,RMVar_hsa_circ_251795,RMVar_hsa_circ_251797,RMVar_hsa_circ_251796,RMVar_hsa_circ_251793,RMVar_hsa_circ_251794,RMVar_hsa_circ_348054,RMVar_hsa_circ_370434,RMVar_hsa_circ_329249,RMVar_hsa_circ_61996,RMVar_hsa_circ_90465,RMVar_hsa_circ_12997,RMVar_hsa_circ_15990,RMVar_hsa_circ_265144,RMVar_hsa_circ_251818,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_370118,RMVar_hsa_circ_76511,RMVar_hsa_circ_251824,RMVar_hsa_circ_251825,RMVar_hsa_circ_251823 28979 RMVar_ID_28979 Human_SNP_ID_362074635 A-to-I Human chr8 - 47780772 47780772 47780772 CACCATGCCCAGCTAATTTTTGTATTTTTAGTAGGGATGGGATTTCACTATGTTGGCCAGGATGA CACCATGCCCAGCTAATTTTTGTATTTTTAGTCGGGATGGGATTTCACTATGTTGGCCAGGATGA T G PRKDC Ensembl:ENSG00000253729 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs759132908 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110783,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_117587,RMVar_hsa_circ_110848,RMVar_hsa_circ_251807,RMVar_hsa_circ_99346,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_93636,RMVar_hsa_circ_95042,RMVar_hsa_circ_92986,RMVar_hsa_circ_251811,RMVar_hsa_circ_251815,RMVar_hsa_circ_84002,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_251803,RMVar_hsa_circ_251805,RMVar_hsa_circ_251806,RMVar_hsa_circ_251804,RMVar_hsa_circ_251801,RMVar_hsa_circ_251802,RMVar_hsa_circ_251800,RMVar_hsa_circ_251795,RMVar_hsa_circ_251797,RMVar_hsa_circ_251796,RMVar_hsa_circ_251793,RMVar_hsa_circ_251794,RMVar_hsa_circ_348054,RMVar_hsa_circ_370434,RMVar_hsa_circ_329249,RMVar_hsa_circ_61996,RMVar_hsa_circ_90465,RMVar_hsa_circ_12997,RMVar_hsa_circ_15990,RMVar_hsa_circ_265144,RMVar_hsa_circ_251818,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_370118,RMVar_hsa_circ_76511,RMVar_hsa_circ_251824,RMVar_hsa_circ_251825,RMVar_hsa_circ_251823 28980 RMVar_ID_28980 Human_SNP_ID_362074663 A-to-I Human chr8 - 47780851 47780851 47780851 TCACTGTGGTCTCCGCTTCCCGGGTTCCAGCAATTCTCCTGCCTCAGCCTTCCGAGTAGCTGAGA TCACTGTGGTCTCCGCTTCCCGGGTTCCAGCAGTTCTCCTGCCTCAGCCTTCCGAGTAGCTGAGA T C PRKDC Ensembl:ENSG00000253729 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs904436120 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26173325 RMVar_hsa_circ_110783,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_117587,RMVar_hsa_circ_110848,RMVar_hsa_circ_251807,RMVar_hsa_circ_99346,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_93636,RMVar_hsa_circ_95042,RMVar_hsa_circ_92986,RMVar_hsa_circ_251811,RMVar_hsa_circ_251815,RMVar_hsa_circ_84002,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_251803,RMVar_hsa_circ_251805,RMVar_hsa_circ_251806,RMVar_hsa_circ_251804,RMVar_hsa_circ_251801,RMVar_hsa_circ_251802,RMVar_hsa_circ_251800,RMVar_hsa_circ_251795,RMVar_hsa_circ_251797,RMVar_hsa_circ_251796,RMVar_hsa_circ_251793,RMVar_hsa_circ_251794,RMVar_hsa_circ_348054,RMVar_hsa_circ_370434,RMVar_hsa_circ_329249,RMVar_hsa_circ_61996,RMVar_hsa_circ_90465,RMVar_hsa_circ_12997,RMVar_hsa_circ_15990,RMVar_hsa_circ_265144,RMVar_hsa_circ_251818,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_370118,RMVar_hsa_circ_76511,RMVar_hsa_circ_251824,RMVar_hsa_circ_251825,RMVar_hsa_circ_251823 28981 RMVar_ID_28981 Human_SNP_ID_362074665 A-to-I Human chr8 - 47780855 47780855 47780855 CGGCTCACTGTGGTCTCCGCTTCCCGGGTTCCAGCAATTCTCCTGCCTCAGCCTTCCGAGTAGCT CGGCTCACTGTGGTCTCCGCTTCCCGGGTTCCGGCAATTCTCCTGCCTCAGCCTTCCGAGTAGCT T C PRKDC Ensembl:ENSG00000253729 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1161465082 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16426563,Human_RBP_ID_26173325 RMVar_hsa_circ_110783,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_117587,RMVar_hsa_circ_110848,RMVar_hsa_circ_251807,RMVar_hsa_circ_99346,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_93636,RMVar_hsa_circ_95042,RMVar_hsa_circ_92986,RMVar_hsa_circ_251811,RMVar_hsa_circ_251815,RMVar_hsa_circ_84002,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_251803,RMVar_hsa_circ_251805,RMVar_hsa_circ_251806,RMVar_hsa_circ_251804,RMVar_hsa_circ_251801,RMVar_hsa_circ_251802,RMVar_hsa_circ_251800,RMVar_hsa_circ_251795,RMVar_hsa_circ_251797,RMVar_hsa_circ_251796,RMVar_hsa_circ_251793,RMVar_hsa_circ_251794,RMVar_hsa_circ_348054,RMVar_hsa_circ_370434,RMVar_hsa_circ_329249,RMVar_hsa_circ_61996,RMVar_hsa_circ_90465,RMVar_hsa_circ_12997,RMVar_hsa_circ_15990,RMVar_hsa_circ_265144,RMVar_hsa_circ_251818,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_370118,RMVar_hsa_circ_76511,RMVar_hsa_circ_251824,RMVar_hsa_circ_251825,RMVar_hsa_circ_251823 28982 RMVar_ID_28982 Human_SNP_ID_362074681 A-to-I Human chr8 - 47780918 47780915 47780919 TGTTTTGTTTTTTTGAGACAGAGTCTCTCTCTATCACCAGGCTGGAGTGCAGTGGCGTGATCTCG TGTTTTGTTTTTTTGAGACAGAGTCTCTCTC____ACCAGGCTGGAGTGCAGTGGCGTGATCTCG TGATA T PRKDC Ensembl:ENSG00000253729 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs201987627 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_26173329 RMVar_hsa_circ_110783,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_117587,RMVar_hsa_circ_110848,RMVar_hsa_circ_251807,RMVar_hsa_circ_99346,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_93636,RMVar_hsa_circ_95042,RMVar_hsa_circ_92986,RMVar_hsa_circ_251811,RMVar_hsa_circ_251815,RMVar_hsa_circ_84002,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_251803,RMVar_hsa_circ_251805,RMVar_hsa_circ_251806,RMVar_hsa_circ_251804,RMVar_hsa_circ_251801,RMVar_hsa_circ_251802,RMVar_hsa_circ_251800,RMVar_hsa_circ_251795,RMVar_hsa_circ_251797,RMVar_hsa_circ_251796,RMVar_hsa_circ_251793,RMVar_hsa_circ_251794,RMVar_hsa_circ_348054,RMVar_hsa_circ_370434,RMVar_hsa_circ_329249,RMVar_hsa_circ_61996,RMVar_hsa_circ_90465,RMVar_hsa_circ_12997,RMVar_hsa_circ_15990,RMVar_hsa_circ_265144,RMVar_hsa_circ_251818,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_370118,RMVar_hsa_circ_76511,RMVar_hsa_circ_251824,RMVar_hsa_circ_251825,RMVar_hsa_circ_251823 28983 RMVar_ID_28983 Human_SNP_ID_362074682 A-to-I Human chr8 - 47780918 47780918 47780918 TGTTTTGTTTTTTTGAGACAGAGTCTCTCTCTATCACCAGGCTGGAGTGCAGTGGCGTGATCTCG TGTTTTGTTTTTTTGAGACAGAGTCTCTCTCTGTCACCAGGCTGGAGTGCAGTGGCGTGATCTCG T C PRKDC Ensembl:ENSG00000253729 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1189447940 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26173329 RMVar_hsa_circ_110783,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_117587,RMVar_hsa_circ_110848,RMVar_hsa_circ_251807,RMVar_hsa_circ_99346,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_93636,RMVar_hsa_circ_95042,RMVar_hsa_circ_92986,RMVar_hsa_circ_251811,RMVar_hsa_circ_251815,RMVar_hsa_circ_84002,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_251803,RMVar_hsa_circ_251805,RMVar_hsa_circ_251806,RMVar_hsa_circ_251804,RMVar_hsa_circ_251801,RMVar_hsa_circ_251802,RMVar_hsa_circ_251800,RMVar_hsa_circ_251795,RMVar_hsa_circ_251797,RMVar_hsa_circ_251796,RMVar_hsa_circ_251793,RMVar_hsa_circ_251794,RMVar_hsa_circ_348054,RMVar_hsa_circ_370434,RMVar_hsa_circ_329249,RMVar_hsa_circ_61996,RMVar_hsa_circ_90465,RMVar_hsa_circ_12997,RMVar_hsa_circ_15990,RMVar_hsa_circ_265144,RMVar_hsa_circ_251818,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_370118,RMVar_hsa_circ_76511,RMVar_hsa_circ_251824,RMVar_hsa_circ_251825,RMVar_hsa_circ_251823 28984 RMVar_ID_28984 Human_SNP_ID_362101011 A-to-I Human chr8 - 47882524 47882518 47882525 CCGGAAGTATGTGCTTGGGTGCATGTTTGCTTATGTGTGTACATCTGTGTGCTTGTGCATGCATG CCGGAAGTATGTGCTTGGGTGCATGTTTGCT_______GTACATCTGTGTGCTTGTGCATGCATG CACACATA C PRKDC Ensembl:ENSG00000253729 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1303916448 Functional Loss DEL dbSNP153 32..38 33 - - - Human_RBP_ID_5153895,Human_RBP_ID_5328852,Human_RBP_ID_21622987,Human_RBP_ID_21995270,Human_RBP_ID_22484099,Human_RBP_ID_24260198 RMVar_hsa_circ_127746,RMVar_hsa_circ_121996,RMVar_hsa_circ_106991,RMVar_hsa_circ_78885,RMVar_hsa_circ_251795,RMVar_hsa_circ_251797,RMVar_hsa_circ_251796,RMVar_hsa_circ_251794,RMVar_hsa_circ_87587,RMVar_hsa_circ_251822,RMVar_hsa_circ_106499,RMVar_hsa_circ_251830,RMVar_hsa_circ_39715,RMVar_hsa_circ_307126,RMVar_hsa_circ_5041,RMVar_hsa_circ_105650,RMVar_hsa_circ_251851,RMVar_hsa_circ_116027,RMVar_hsa_circ_251852,RMVar_hsa_circ_345838,RMVar_hsa_circ_329007,RMVar_hsa_circ_46665,RMVar_hsa_circ_55489,RMVar_hsa_circ_44349,RMVar_hsa_circ_7896,RMVar_hsa_circ_318603,RMVar_hsa_circ_337032,RMVar_hsa_circ_19420,RMVar_hsa_circ_367114,RMVar_hsa_circ_109931,RMVar_hsa_circ_251869,RMVar_hsa_circ_49336,RMVar_hsa_circ_25121,RMVar_hsa_circ_83644,RMVar_hsa_circ_97782,RMVar_hsa_circ_251882,RMVar_hsa_circ_251883,RMVar_hsa_circ_320705,RMVar_hsa_circ_63975,RMVar_hsa_circ_4727,RMVar_hsa_circ_118487,RMVar_hsa_circ_251887,RMVar_hsa_circ_278859,RMVar_hsa_circ_2460,RMVar_hsa_circ_317693,RMVar_hsa_circ_3819,RMVar_hsa_circ_124024,RMVar_hsa_circ_104502,RMVar_hsa_circ_251891,RMVar_hsa_circ_124666,RMVar_hsa_circ_251892,RMVar_hsa_circ_251893,RMVar_hsa_circ_291898,RMVar_hsa_circ_334414,RMVar_hsa_circ_325289,RMVar_hsa_circ_312019,RMVar_hsa_circ_31034,RMVar_hsa_circ_12030,RMVar_hsa_circ_251897,RMVar_hsa_circ_76361,RMVar_hsa_circ_251896,RMVar_hsa_circ_50675,RMVar_hsa_circ_313886,RMVar_hsa_circ_330245,RMVar_hsa_circ_275945,RMVar_hsa_circ_251898 28985 RMVar_ID_28985 Human_SNP_ID_362101667 A-to-I Human chr8 - 47885280 47885280 47885280 AGGCATGGTGGTGTGTGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATTTCTTGAA AGGCATGGTGGTGTGTGCCTGTAATCCCAGCTGCTCAGGAGGCTGAGGCAGGAGAATTTCTTGAA T C PRKDC Ensembl:ENSG00000253729 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1056825669 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127746,RMVar_hsa_circ_121996,RMVar_hsa_circ_106991,RMVar_hsa_circ_78885,RMVar_hsa_circ_251795,RMVar_hsa_circ_251797,RMVar_hsa_circ_251796,RMVar_hsa_circ_251794,RMVar_hsa_circ_87587,RMVar_hsa_circ_251822,RMVar_hsa_circ_106499,RMVar_hsa_circ_251830,RMVar_hsa_circ_39715,RMVar_hsa_circ_307126,RMVar_hsa_circ_5041,RMVar_hsa_circ_105650,RMVar_hsa_circ_251851,RMVar_hsa_circ_116027,RMVar_hsa_circ_251852,RMVar_hsa_circ_345838,RMVar_hsa_circ_329007,RMVar_hsa_circ_46665,RMVar_hsa_circ_55489,RMVar_hsa_circ_44349,RMVar_hsa_circ_7896,RMVar_hsa_circ_318603,RMVar_hsa_circ_337032,RMVar_hsa_circ_19420,RMVar_hsa_circ_367114,RMVar_hsa_circ_109931,RMVar_hsa_circ_251869,RMVar_hsa_circ_49336,RMVar_hsa_circ_25121,RMVar_hsa_circ_83644,RMVar_hsa_circ_97782,RMVar_hsa_circ_251882,RMVar_hsa_circ_251883,RMVar_hsa_circ_320705,RMVar_hsa_circ_63975,RMVar_hsa_circ_4727,RMVar_hsa_circ_118487,RMVar_hsa_circ_251887,RMVar_hsa_circ_278859,RMVar_hsa_circ_2460,RMVar_hsa_circ_317693,RMVar_hsa_circ_3819,RMVar_hsa_circ_124024,RMVar_hsa_circ_104502,RMVar_hsa_circ_251891,RMVar_hsa_circ_124666,RMVar_hsa_circ_251892,RMVar_hsa_circ_251893,RMVar_hsa_circ_291898,RMVar_hsa_circ_334414,RMVar_hsa_circ_325289,RMVar_hsa_circ_312019,RMVar_hsa_circ_31034,RMVar_hsa_circ_12030,RMVar_hsa_circ_251897,RMVar_hsa_circ_76361,RMVar_hsa_circ_251896,RMVar_hsa_circ_50675,RMVar_hsa_circ_313886,RMVar_hsa_circ_330245,RMVar_hsa_circ_275945,RMVar_hsa_circ_251898 28986 RMVar_ID_28986 Human_SNP_ID_362101797 A-to-I Human chr8 - 47885780 47885780 47885780 TGAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCACCCGCCACCACACCTA TGAAGCGATTCTCCTGCCTCAGCCTCCCGAGTGGCTGGGATTACAGGCACCCGCCACCACACCTA T C PRKDC Ensembl:ENSG00000253729 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1437705177 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26174275 RMVar_hsa_circ_127746,RMVar_hsa_circ_121996,RMVar_hsa_circ_106991,RMVar_hsa_circ_78885,RMVar_hsa_circ_251795,RMVar_hsa_circ_251797,RMVar_hsa_circ_251796,RMVar_hsa_circ_251794,RMVar_hsa_circ_87587,RMVar_hsa_circ_251822,RMVar_hsa_circ_106499,RMVar_hsa_circ_251830,RMVar_hsa_circ_39715,RMVar_hsa_circ_307126,RMVar_hsa_circ_5041,RMVar_hsa_circ_105650,RMVar_hsa_circ_251851,RMVar_hsa_circ_116027,RMVar_hsa_circ_251852,RMVar_hsa_circ_345838,RMVar_hsa_circ_329007,RMVar_hsa_circ_46665,RMVar_hsa_circ_55489,RMVar_hsa_circ_44349,RMVar_hsa_circ_7896,RMVar_hsa_circ_318603,RMVar_hsa_circ_337032,RMVar_hsa_circ_19420,RMVar_hsa_circ_367114,RMVar_hsa_circ_109931,RMVar_hsa_circ_251869,RMVar_hsa_circ_49336,RMVar_hsa_circ_25121,RMVar_hsa_circ_83644,RMVar_hsa_circ_97782,RMVar_hsa_circ_251882,RMVar_hsa_circ_251883,RMVar_hsa_circ_320705,RMVar_hsa_circ_63975,RMVar_hsa_circ_4727,RMVar_hsa_circ_118487,RMVar_hsa_circ_251887,RMVar_hsa_circ_278859,RMVar_hsa_circ_2460,RMVar_hsa_circ_317693,RMVar_hsa_circ_3819,RMVar_hsa_circ_124024,RMVar_hsa_circ_104502,RMVar_hsa_circ_251891,RMVar_hsa_circ_124666,RMVar_hsa_circ_251892,RMVar_hsa_circ_251893,RMVar_hsa_circ_291898,RMVar_hsa_circ_334414,RMVar_hsa_circ_325289,RMVar_hsa_circ_312019,RMVar_hsa_circ_31034,RMVar_hsa_circ_12030,RMVar_hsa_circ_251897,RMVar_hsa_circ_76361,RMVar_hsa_circ_251896,RMVar_hsa_circ_50675,RMVar_hsa_circ_313886,RMVar_hsa_circ_330245,RMVar_hsa_circ_275945,RMVar_hsa_circ_251898 28987 RMVar_ID_28987 Human_SNP_ID_362101814 A-to-I Human chr8 - 47885845 47885845 47885845 CACTTTCGCCCAGGCTGGAGTGCAGTGGCACGATCTCTGCTGACTGCAACCTCTGCATCCCAGAT CACTTTCGCCCAGGCTGGAGTGCAGTGGCACGGTCTCTGCTGACTGCAACCTCTGCATCCCAGAT T C PRKDC Ensembl:ENSG00000253729 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs565639070 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127746,RMVar_hsa_circ_121996,RMVar_hsa_circ_106991,RMVar_hsa_circ_78885,RMVar_hsa_circ_251795,RMVar_hsa_circ_251797,RMVar_hsa_circ_251796,RMVar_hsa_circ_251794,RMVar_hsa_circ_87587,RMVar_hsa_circ_251822,RMVar_hsa_circ_106499,RMVar_hsa_circ_251830,RMVar_hsa_circ_39715,RMVar_hsa_circ_307126,RMVar_hsa_circ_5041,RMVar_hsa_circ_105650,RMVar_hsa_circ_251851,RMVar_hsa_circ_116027,RMVar_hsa_circ_251852,RMVar_hsa_circ_345838,RMVar_hsa_circ_329007,RMVar_hsa_circ_46665,RMVar_hsa_circ_55489,RMVar_hsa_circ_44349,RMVar_hsa_circ_7896,RMVar_hsa_circ_318603,RMVar_hsa_circ_337032,RMVar_hsa_circ_19420,RMVar_hsa_circ_367114,RMVar_hsa_circ_109931,RMVar_hsa_circ_251869,RMVar_hsa_circ_49336,RMVar_hsa_circ_25121,RMVar_hsa_circ_83644,RMVar_hsa_circ_97782,RMVar_hsa_circ_251882,RMVar_hsa_circ_251883,RMVar_hsa_circ_320705,RMVar_hsa_circ_63975,RMVar_hsa_circ_4727,RMVar_hsa_circ_118487,RMVar_hsa_circ_251887,RMVar_hsa_circ_278859,RMVar_hsa_circ_2460,RMVar_hsa_circ_317693,RMVar_hsa_circ_3819,RMVar_hsa_circ_124024,RMVar_hsa_circ_104502,RMVar_hsa_circ_251891,RMVar_hsa_circ_124666,RMVar_hsa_circ_251892,RMVar_hsa_circ_251893,RMVar_hsa_circ_291898,RMVar_hsa_circ_334414,RMVar_hsa_circ_325289,RMVar_hsa_circ_312019,RMVar_hsa_circ_31034,RMVar_hsa_circ_12030,RMVar_hsa_circ_251897,RMVar_hsa_circ_76361,RMVar_hsa_circ_251896,RMVar_hsa_circ_50675,RMVar_hsa_circ_313886,RMVar_hsa_circ_330245,RMVar_hsa_circ_275945,RMVar_hsa_circ_251898 28988 RMVar_ID_28988 Human_SNP_ID_362103604 A-to-I Human chr8 - 47892043 47892043 47892043 CAACATGGCGAAATCCCGTATCTACCAAAAATACAAAAATTAGTCAGGCATGGTGGCAGGTCCCT CAACATGGCGAAATCCCGTATCTACCAAAAATTCAAAAATTAGTCAGGCATGGTGGCAGGTCCCT T A PRKDC Ensembl:ENSG00000253729 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1055158746 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118,RMVar_hsa_circ_39715,RMVar_hsa_circ_307126,RMVar_hsa_circ_5041,RMVar_hsa_circ_345838,RMVar_hsa_circ_329007,RMVar_hsa_circ_46665,RMVar_hsa_circ_55489,RMVar_hsa_circ_44349,RMVar_hsa_circ_7896,RMVar_hsa_circ_318603,RMVar_hsa_circ_337032,RMVar_hsa_circ_367114,RMVar_hsa_circ_49336,RMVar_hsa_circ_25121,RMVar_hsa_circ_320705,RMVar_hsa_circ_63975,RMVar_hsa_circ_4727,RMVar_hsa_circ_278859,RMVar_hsa_circ_317693,RMVar_hsa_circ_3819,RMVar_hsa_circ_291898,RMVar_hsa_circ_325289,RMVar_hsa_circ_312019,RMVar_hsa_circ_31034,RMVar_hsa_circ_50675,RMVar_hsa_circ_313886,RMVar_hsa_circ_12443,RMVar_hsa_circ_22579,RMVar_hsa_circ_44665,RMVar_hsa_circ_20812,RMVar_hsa_circ_6951,RMVar_hsa_circ_332196,RMVar_hsa_circ_7693,RMVar_hsa_circ_24652,RMVar_hsa_circ_295761 28989 RMVar_ID_28989 Human_SNP_ID_362115508 A-to-I Human chr8 - 47936679 47936679 47936679 CTGGGAGTTGGAGGTTGTGGTGAGCTGAGATCACGCCATTGCACTCCAGCCTGGACAAGAGCGAA CTGGGAGTTGGAGGTTGTGGTGAGCTGAGATCGCGCCATTGCACTCCAGCCTGGACAAGAGCGAA T C PRKDC Ensembl:ENSG00000253729 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991600428 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39715,RMVar_hsa_circ_5464,RMVar_hsa_circ_75887,RMVar_hsa_circ_24652,RMVar_hsa_circ_61234,RMVar_hsa_circ_96637,RMVar_hsa_circ_88681,RMVar_hsa_circ_92750,RMVar_hsa_circ_87085,RMVar_hsa_circ_251904,RMVar_hsa_circ_251905,RMVar_hsa_circ_251902,RMVar_hsa_circ_251903,RMVar_hsa_circ_251901,RMVar_hsa_circ_81016,RMVar_hsa_circ_97106,RMVar_hsa_circ_113996,RMVar_hsa_circ_251915,RMVar_hsa_circ_251916,RMVar_hsa_circ_251917,RMVar_hsa_circ_267168,RMVar_hsa_circ_98984,RMVar_hsa_circ_110167,RMVar_hsa_circ_251928,RMVar_hsa_circ_251929,RMVar_hsa_circ_267210,RMVar_hsa_circ_113514,RMVar_hsa_circ_27732,RMVar_hsa_circ_251930,RMVar_hsa_circ_375398,RMVar_hsa_circ_369481,RMVar_hsa_circ_88331,RMVar_hsa_circ_51447,RMVar_hsa_circ_251937,RMVar_hsa_circ_251939,RMVar_hsa_circ_251938,RMVar_hsa_circ_102246,RMVar_hsa_circ_110232,RMVar_hsa_circ_322419,RMVar_hsa_circ_351267,RMVar_hsa_circ_251949,RMVar_hsa_circ_58991,RMVar_hsa_circ_91368,RMVar_hsa_circ_251957,RMVar_hsa_circ_251959,RMVar_hsa_circ_32533,RMVar_hsa_circ_251958,RMVar_hsa_circ_54674,RMVar_hsa_circ_79236,RMVar_hsa_circ_50895,RMVar_hsa_circ_251961,RMVar_hsa_circ_349144,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_89484,RMVar_hsa_circ_374161,RMVar_hsa_circ_251972,RMVar_hsa_circ_113617,RMVar_hsa_circ_251975,RMVar_hsa_circ_85235,RMVar_hsa_circ_251976,RMVar_hsa_circ_251974 28990 RMVar_ID_28990 Human_SNP_ID_362115887 A-to-I Human chr8 - 47938033 47938033 47938033 CATAACTCACTGTAGCCCTGACCTCTAGGGCTAAGCAATCCTGCTGCCTTAACTTCCCGAGTAAC CATAACTCACTGTAGCCCTGACCTCTAGGGCTGAGCAATCCTGCTGCCTTAACTTCCCGAGTAAC T C PRKDC Ensembl:ENSG00000253729 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934309296 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16430337 RMVar_hsa_circ_39715,RMVar_hsa_circ_5464,RMVar_hsa_circ_75887,RMVar_hsa_circ_24652,RMVar_hsa_circ_61234,RMVar_hsa_circ_96637,RMVar_hsa_circ_88681,RMVar_hsa_circ_92750,RMVar_hsa_circ_87085,RMVar_hsa_circ_251904,RMVar_hsa_circ_251905,RMVar_hsa_circ_251902,RMVar_hsa_circ_251903,RMVar_hsa_circ_251901,RMVar_hsa_circ_81016,RMVar_hsa_circ_97106,RMVar_hsa_circ_113996,RMVar_hsa_circ_251915,RMVar_hsa_circ_251916,RMVar_hsa_circ_251917,RMVar_hsa_circ_267168,RMVar_hsa_circ_98984,RMVar_hsa_circ_110167,RMVar_hsa_circ_251928,RMVar_hsa_circ_251929,RMVar_hsa_circ_267210,RMVar_hsa_circ_113514,RMVar_hsa_circ_27732,RMVar_hsa_circ_251930,RMVar_hsa_circ_375398,RMVar_hsa_circ_369481,RMVar_hsa_circ_88331,RMVar_hsa_circ_51447,RMVar_hsa_circ_251937,RMVar_hsa_circ_251939,RMVar_hsa_circ_251938,RMVar_hsa_circ_102246,RMVar_hsa_circ_110232,RMVar_hsa_circ_322419,RMVar_hsa_circ_351267,RMVar_hsa_circ_251949,RMVar_hsa_circ_58991,RMVar_hsa_circ_91368,RMVar_hsa_circ_251957,RMVar_hsa_circ_251959,RMVar_hsa_circ_32533,RMVar_hsa_circ_251958,RMVar_hsa_circ_54674,RMVar_hsa_circ_79236,RMVar_hsa_circ_50895,RMVar_hsa_circ_251961,RMVar_hsa_circ_349144,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_89484,RMVar_hsa_circ_374161,RMVar_hsa_circ_251972,RMVar_hsa_circ_113617,RMVar_hsa_circ_251975,RMVar_hsa_circ_85235,RMVar_hsa_circ_251976,RMVar_hsa_circ_251974 28991 RMVar_ID_28991 Human_SNP_ID_362118130 A-to-I Human chr8 - 47946167 47946167 47946167 GCCACCACACCCAGCTAATTTTTCCTATTTTTAGTAGAGACGGGGTTTCACTGTGTTGGCCAGGC GCCACCACACCCAGCTAATTTTTCCTATTTTTGGTAGAGACGGGGTTTCACTGTGTTGGCCAGGC T C PRKDC Ensembl:ENSG00000253729 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1356279881 Functional Loss SNV dbSNP153 33..33 33 - - - 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 28992 RMVar_ID_28992 Human_SNP_ID_362118485 A-to-I Human chr8 - 47947585 47947585 47947585 TTTTGTATTTTTTGTAGAGATGGGGTTTCACCATGTCGGTCAGGCTTGTCTTGAACTCCTGAGCT TTTTGTATTTTTTGTAGAGATGGGGTTTCACCTTGTCGGTCAGGCTTGTCTTGAACTCCTGAGCT T A PRKDC Ensembl:ENSG00000253729 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1317417103 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16430703,Human_RBP_ID_17578644 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 28993 RMVar_ID_28993 Human_SNP_ID_362118531 A-to-I Human chr8 - 47947742 47947742 47947742 TGCCATGTCCAGCTAATTTTTGTGTTTTTAGTAGAGACGGGGTTTCACCATGTTGCCCAGGCTGG TGCCATGTCCAGCTAATTTTTGTGTTTTTAGTGGAGACGGGGTTTCACCATGTTGCCCAGGCTGG T C PRKDC Ensembl:ENSG00000253729 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs368337469 Functional Loss SNV dbSNP153 33..33 33 - - - 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 28994 RMVar_ID_28994 Human_SNP_ID_362118550 A-to-I Human chr8 - 47947845 47947845 47947845 GGAGTGCAGTGGCGCGATCTTGGCTCACTGTAACCTCTGCCTCCCACGTTCAAGTGATTCTTGTG GGAGTGCAGTGGCGCGATCTTGGCTCACTGTATCCTCTGCCTCCCACGTTCAAGTGATTCTTGTG T A PRKDC Ensembl:ENSG00000253729 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs561793599 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16430710,Human_RBP_ID_22732651 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 28995 RMVar_ID_28995 Human_SNP_ID_362121828 A-to-I Human chr8 - 47958874 47958874 47958874 AAAATTAACTGGGCATGGTGGCGAGCGCCTGTAGTCCCAGCTATTCGGGAGGCTGAGACAGGAGA AAAATTAACTGGGCATGGTGGCGAGCGCCTGTGGTCCCAGCTATTCGGGAGGCTGAGACAGGAGA T C PRKDC Ensembl:ENSG00000253729 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1012262664 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97106,RMVar_hsa_circ_251917,RMVar_hsa_circ_98984,RMVar_hsa_circ_251929,RMVar_hsa_circ_91368,RMVar_hsa_circ_251959 28996 RMVar_ID_28996 Human_SNP_ID_362127922 A-to-I Human chr8 + 47977111 47977111 47977111 GATGGTGAAACCCCGTCTCTAGTAAAGATAACAAAAAATTAGCTGGGCTTGATGGCATGCGCCTG GATGGTGAAACCCCGTCTCTAGTAAAGATAACGAAAAATTAGCTGGGCTTGATGGCATGCGCCTG A G MCM4 Ensembl:ENSG00000104738 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1466468369 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4988033,Human_RBP_ID_7841573,Human_RBP_ID_16431773,Human_RBP_ID_18119603,Human_RBP_ID_18391100,Human_RBP_ID_24520573,Human_RBP_ID_27538858,Human_RBP_ID_27777653 RMVar_hsa_circ_93440,RMVar_hsa_circ_251983 28997 RMVar_ID_28997 Human_SNP_ID_362128077 A-to-I Human chr8 + 47977633 47977633 47977633 GGTGTATGTCACTATGCCCGGCTACTTTTTGTATTTTTTGGTAGAGACGGCTTCGCCACGTTGCC GGTGTATGTCACTATGCCCGGCTACTTTTTGTGTTTTTTGGTAGAGACGGCTTCGCCACGTTGCC A G MCM4 Ensembl:ENSG00000104738 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs943956114 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_700787,Human_RBP_ID_7841591,Human_RBP_ID_16431802,Human_RBP_ID_18391111,Human_RBP_ID_23086692,Human_RBP_ID_24520579,Human_RBP_ID_27125554 RMVar_hsa_circ_93440,RMVar_hsa_circ_251983 28998 RMVar_ID_28998 Human_SNP_ID_362128097 A-to-I Human chr8 + 47977687 47977687 47977687 GCCACGTTGCCCAGGCTGCAAGCGATATGCCTAGGCTCAAGCGATCTGCCCACCTCAACTTCCGG GCCACGTTGCCCAGGCTGCAAGCGATATGCCTGGGCTCAAGCGATCTGCCCACCTCAACTTCCGG A G MCM4 Ensembl:ENSG00000104738 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1135031 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_700790,Human_RBP_ID_7841594,Human_RBP_ID_16431804,Human_RBP_ID_18391112,Human_RBP_ID_18897481,Human_RBP_ID_22837080,Human_RBP_ID_23316141,Human_RBP_ID_26556306 RMVar_hsa_circ_93440,RMVar_hsa_circ_251983 28999 RMVar_ID_28999 Human_SNP_ID_362128113 A-to-I Human chr8 + 47977733 47977733 47977733 TGCCCACCTCAACTTCCGGAAGTGCTGAGATTACAGGTGTGAGCCACTGCACCCAGCCTTTGTTT TGCCCACCTCAACTTCCGGAAGTGCTGAGATTGCAGGTGTGAGCCACTGCACCCAGCCTTTGTTT A G MCM4 Ensembl:ENSG00000104738 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs529512295 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_700790,Human_RBP_ID_7841594,Human_RBP_ID_16431804,Human_RBP_ID_24260517 Human_miRNA_ID_2230703,Human_miRNA_ID_2450224 Clinvar_Rec_97 RMVar_hsa_circ_93440,RMVar_hsa_circ_251983 29000 RMVar_ID_29000 Human_SNP_ID_362137297 A-to-I Human chr8 + 48012532 48012525 48012533 CCTGAGGTCGGGAGGTTGAGACCAGCTGGACCAACATGGAGAAACCATGTCTCTACTAAAAATAC CCTGAGGTCGGGAGGTTGAGACCAGC________CATGGAGAAACCATGTCTCTACTAAAAATAC CTGGACCAA C UBE2V2 Ensembl:ENSG00000169139 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs567963414 Functional Loss DEL dbSNP153 27..34 33 - - - RMVar_hsa_circ_82333,RMVar_hsa_circ_252006 29001 RMVar_ID_29001 Human_SNP_ID_362137543 A-to-I Human chr8 + 48013447 48013447 48013447 CTGTGGCCTCAGCCTCCGAAGTAGCTGGGACTATAGGCGCCTGCCACCATGCCCGGTTAATTTTT CTGTGGCCTCAGCCTCCGAAGTAGCTGGGACTGTAGGCGCCTGCCACCATGCCCGGTTAATTTTT A G UBE2V2 Ensembl:ENSG00000169139 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879816420 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82333,RMVar_hsa_circ_252006 29002 RMVar_ID_29002 Human_SNP_ID_362137651 A-to-I Human chr8 + 48013840 48013840 48013840 AGCATTGTATATACTGGAAGAACTAGTTTAGCAGTGTTCTGAGTTCCCTGCTGCCCCTGACAGAC AGCATTGTATATACTGGAAGAACTAGTTTAGCGGTGTTCTGAGTTCCCTGCTGCCCCTGACAGAC A G UBE2V2 Ensembl:ENSG00000169139 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355818921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16432070 RMVar_hsa_circ_82333,RMVar_hsa_circ_252006 29003 RMVar_ID_29003 Human_SNP_ID_362139135 A-to-I Human chr8 + 48019218 48019218 48019218 GAAACCCCATCTCTACTAAAAATACAAAAATTAGCCAGGTGTGGTGGCGGGCGCCTGTGACCCCA GAAACCCCATCTCTACTAAAAATACAAAAATTGGCCAGGTGTGGTGGCGGGCGCCTGTGACCCCA A G UBE2V2 Ensembl:ENSG00000169139 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs552618372 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82333,RMVar_hsa_circ_252006 29004 RMVar_ID_29004 Human_SNP_ID_362139544 A-to-I Human chr8 + 48020739 48020739 48020739 GCCGTCTTCTTGCCTCAGCCTTTGGAGTAGCTAGGACTATAGGTGTGTGCCACCAAACCTGGCTA GCCGTCTTCTTGCCTCAGCCTTTGGAGTAGCTGGGACTATAGGTGTGTGCCACCAAACCTGGCTA A G UBE2V2 Ensembl:ENSG00000169139 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1042415515 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82333,RMVar_hsa_circ_252006 29005 RMVar_ID_29005 Human_SNP_ID_362140287 A-to-I Human chr8 + 48023638 48023638 48023638 TTACGCCTGTAATCCCAGCACTTTGGAAGGCCAAGGCAGGAGGATCACTTGAGGTCAGGAGTTTG TTACGCCTGTAATCCCAGCACTTTGGAAGGCCGAGGCAGGAGGATCACTTGAGGTCAGGAGTTTG A G UBE2V2 Ensembl:ENSG00000169139 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1398557840 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82333,RMVar_hsa_circ_252006 29006 RMVar_ID_29006 Human_SNP_ID_362141671 A-to-I Human chr8 + 48029094 48029094 48029094 AATAATGTTCAGGCCAGGTGCAGTAGGAGGCCAAGGTAGGCAGATCACTTGAGGTCAGGAGTTTG AATAATGTTCAGGCCAGGTGCAGTAGGAGGCCGAGGTAGGCAGATCACTTGAGGTCAGGAGTTTG A G UBE2V2 Ensembl:ENSG00000169139 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs907882740 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_255039,Human_RBP_ID_16432491 RMVar_hsa_circ_82333,RMVar_hsa_circ_252006 29007 RMVar_ID_29007 Human_SNP_ID_362142700 A-to-I Human chr8 + 48033696 48033696 48033696 TTAAAAGTCCTCATGGCTGGGTGCGGGCTCATATCTATAATCCTAGCACTTTGGGAGGCCGAGGC TTAAAAGTCCTCATGGCTGGGTGCGGGCTCATGTCTATAATCCTAGCACTTTGGGAGGCCGAGGC A G UBE2V2 Ensembl:ENSG00000169139 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs771065110 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82333,RMVar_hsa_circ_252006 29008 RMVar_ID_29008 Human_SNP_ID_362142721 A-to-I Human chr8 + 48033793 48033793 48033793 TAGCCTGGGCAACATGGCAAAACCCCGTCTCTACAAAAAATACAAAAATTACCTTGCATGTTGGC TAGCCTGGGCAACATGGCAAAACCCCGTCTCTGCAAAAAATACAAAAATTACCTTGCATGTTGGC A G UBE2V2 Ensembl:ENSG00000169139 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1416088475 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82333,RMVar_hsa_circ_252006 29009 RMVar_ID_29009 Human_SNP_ID_362143499 A-to-I Human chr8 + 48036094 48036094 48036094 CTTCCATGTTAGCCTCCGGAGCAGCTCAGACTACAGCTGTGCACCACCATGCCTGGCTAATTTTT CTTCCATGTTAGCCTCCGGAGCAGCTCAGACTGCAGCTGTGCACCACCATGCCTGGCTAATTTTT A G UBE2V2 Ensembl:ENSG00000169139 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs945816252 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16432614 RMVar_hsa_circ_82333,RMVar_hsa_circ_252006 29010 RMVar_ID_29010 Human_SNP_ID_362147028 A-to-I Human chr8 + 48050290 48050290 48050290 AGAGTCTCACTCTGTCACCCAGGCTGGAGTACAATTGTGCGATCTTGGCTCACTGCAACCTCTGC AGAGTCTCACTCTGTCACCCAGGCTGGAGTACTATTGTGCGATCTTGGCTCACTGCAACCTCTGC A T UBE2V2 Ensembl:ENSG00000169139 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223538295 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_975876 RMVar_hsa_circ_82333,RMVar_hsa_circ_252006,RMVar_hsa_circ_252008 29011 RMVar_ID_29011 Human_SNP_ID_362149411 A-to-I Human chr8 + 48060116 48060116 48060116 TAATCCCAGCTACTTGGGAGGCCTCATGAGGCAGGAGAATTTCTTGAACCTGGGAGGCGGAAGTT TAATCCCAGCTACTTGGGAGGCCTCATGAGGCCGGAGAATTTCTTGAACCTGGGAGGCGGAAGTT A C UBE2V2 Ensembl:ENSG00000169139 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs940430060 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82333,RMVar_hsa_circ_252006,RMVar_hsa_circ_252008 29012 RMVar_ID_29012 Human_SNP_ID_362648697 A-to-I Human chr8 + 49957868 49957868 49957868 TGTGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGACTAGAGGATGGTTTGAACCGGGAGTTGAAG TGTGCCTGTAGTCCCAGCTACTCAGGAGGCTGCGACTAGAGGATGGTTTGAACCGGGAGTTGAAG A C SNTG1 Ensembl:ENSG00000147481 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs759810103 Functional Loss SNV dbSNP153 33..33 33 - - - 29013 RMVar_ID_29013 Human_SNP_ID_362686353 A-to-I Human chr8 + 50094934 50094934 50094934 CAGCCTATCTGCCCATCAATGGTAAACTGGATAAAGAAAATGTGGCACATATACACCATAGACTA CAGCCTATCTGCCCATCAATGGTAAACTGGATGAAGAAAATGTGGCACATATACACCATAGACTA A G SNTG1 Ensembl:ENSG00000147481 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1272008831 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_344129 29014 RMVar_ID_29014 Human_SNP_ID_363149748 A-to-I Human chr8 - 51821213 51821213 51821213 ATCACCTGAGCCTGGGTGGTTGAGGCTCCAGTAGGCCATGATTGTGCCATCACACTTCAGCCTGG ATCACCTGAGCCTGGGTGGTTGAGGCTCCAGTGGGCCATGATTGTGCCATCACACTTCAGCCTGG T C PCMTD1 Ensembl:ENSG00000168300 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1022015036 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17578648 RMVar_hsa_circ_124656,RMVar_hsa_circ_252044,RMVar_hsa_circ_252045,RMVar_hsa_circ_252046 29015 RMVar_ID_29015 Human_SNP_ID_363149782 A-to-I Human chr8 - 51821338 51821338 51821338 TCAGGAGTTAAAGAGACCTGCCTAGGCAATATAGTGAGATCCCGTTTCAACAAATAATTTAAAAA TCAGGAGTTAAAGAGACCTGCCTAGGCAATATGGTGAGATCCCGTTTCAACAAATAATTTAAAAA T C PCMTD1 Ensembl:ENSG00000168300 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956990294 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124656,RMVar_hsa_circ_252044,RMVar_hsa_circ_252045,RMVar_hsa_circ_252046 29016 RMVar_ID_29016 Human_SNP_ID_363158158 A-to-I Human chr8 - 51854711 51854711 51854711 CGCCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACTGTGTTGGGCAAGATGG CGCCATGCCCAGCTAATTTTTGTATTTTTAGTGGAGACGGGGTTTCACTGTGTTGGGCAAGATGG T C PCMTD1 Ensembl:ENSG00000168300 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1257147076 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16433943,Human_RBP_ID_24260899 RMVar_hsa_circ_252047,RMVar_hsa_circ_295213,RMVar_hsa_circ_124656,RMVar_hsa_circ_252045,RMVar_hsa_circ_252046,RMVar_hsa_circ_252052,RMVar_hsa_circ_252051,RMVar_hsa_circ_370827,RMVar_hsa_circ_295411,RMVar_hsa_circ_252050 29017 RMVar_ID_29017 Human_SNP_ID_363158517 A-to-I Human chr8 - 51855788 51855788 51855788 AGGCATGGTGGCAGGCGCCTGTAGTTGCAGCTACTCGGGAGGCTGAGGGCAGGAGAATGGTGTGA AGGCATGGTGGCAGGCGCCTGTAGTTGCAGCTGCTCGGGAGGCTGAGGGCAGGAGAATGGTGTGA T C PCMTD1 Ensembl:ENSG00000168300 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251322535 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_252047,RMVar_hsa_circ_295213,RMVar_hsa_circ_124656,RMVar_hsa_circ_252045,RMVar_hsa_circ_252046,RMVar_hsa_circ_252052,RMVar_hsa_circ_252051,RMVar_hsa_circ_370827,RMVar_hsa_circ_295411,RMVar_hsa_circ_252050 29018 RMVar_ID_29018 Human_SNP_ID_363165651 A-to-I Human chr8 - 51883402 51883401 51883403 ATATATGCATATATATACATTTTACTCTTAATAACAATCTCCCCACTTGCTAGCCTTAGGACACT ATATATGCATATATATACATTTTACTCTTAA__ACAATCTCCCCACTTGCTAGCCTTAGGACACT TTA T PCMTD1 Ensembl:ENSG00000168300 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1480212251 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_3161861,Human_RBP_ID_16434272 RMVar_hsa_circ_124656,RMVar_hsa_circ_252046 29019 RMVar_ID_29019 Human_SNP_ID_363170346 A-to-I Human chr8 + 51900028 51900028 51900028 CCTGTAGTCCCAGCAACTCGGGAGGCTGAGGTAGGAGAATCGCTTGAACCCGGGAGTCGGAGGTT CCTGTAGTCCCAGCAACTCGGGAGGCTGAGGTGGGAGAATCGCTTGAACCCGGGAGTCGGAGGTT A G AC064807.1 Ensembl:ENSG00000228801 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs960357164 Functional Loss SNV dbSNP153 33..33 33 - - - 29020 RMVar_ID_29020 Human_SNP_ID_363170705 A-to-I Human chr8 + 51901373 51901373 51901373 CAAGCAGTTCTGCCTCAGCCTCCCAAGTAGCTAGGATCACAGGAGCGCACCACCACCCCCTGCTA CAAGCAGTTCTGCCTCAGCCTCCCAAGTAGCTGGGATCACAGGAGCGCACCACCACCCCCTGCTA A G AC064807.1 Ensembl:ENSG00000228801 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1190553690 Functional Loss SNV dbSNP153 33..33 33 - - - 29021 RMVar_ID_29021 Human_SNP_ID_363170722 A-to-I Human chr8 + 51901420 51901413 51901420 CACCACCACCCCCTGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCCCCTGTTGGCTAGGCT CACCACCACCCCCTGCTAATTTTTGT_______GTAGAGATGGGGTTTCCCCTGTTGGCTAGGCT TATTTTTA T AC064807.1 Ensembl:ENSG00000228801 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1360117893 Functional Loss DEL dbSNP153 27..33 33 - - - 29022 RMVar_ID_29022 Human_SNP_ID_363229738 A-to-I Human chr8 - 52138053 52138053 52138053 GTTTTACTCTTGTTGCCCAGTGCAATGGTGCAATCTCGGCTCACCACAATGTCCGCCTCCTGAGT GTTTTACTCTTGTTGCCCAGTGCAATGGTGCAGTCTCGGCTCACCACAATGTCCGCCTCCTGAGT T C ST18 Ensembl:ENSG00000147488 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1375728455 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266890,RMVar_hsa_circ_71769,RMVar_hsa_circ_9751,RMVar_hsa_circ_14201,RMVar_hsa_circ_252057,RMVar_hsa_circ_27256,RMVar_hsa_circ_5889,RMVar_hsa_circ_252060,RMVar_hsa_circ_7986 29023 RMVar_ID_29023 Human_SNP_ID_363273936 A-to-I Human chr8 - 52317473 52317473 52317473 AATATGTCCTCTTACAGTTCTGGAGACTAGAAATCTGAAATCAAGGTGTTGGCAGGGCCATGCTC AATATGTCCTCTTACAGTTCTGGAGACTAGAATTCTGAAATCAAGGTGTTGGCAGGGCCATGCTC T A ST18 Ensembl:ENSG00000147488 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs963087337 Functional Loss SNV dbSNP153 33..33 33 - - - 29024 RMVar_ID_29024 Human_SNP_ID_363273937 A-to-I Human chr8 - 52317473 52317473 52317473 AATATGTCCTCTTACAGTTCTGGAGACTAGAAATCTGAAATCAAGGTGTTGGCAGGGCCATGCTC AATATGTCCTCTTACAGTTCTGGAGACTAGAAGTCTGAAATCAAGGTGTTGGCAGGGCCATGCTC T C ST18 Ensembl:ENSG00000147488 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs963087337 Functional Loss SNV dbSNP153 33..33 33 - - - 29025 RMVar_ID_29025 Human_SNP_ID_363374667 A-to-I Human chr8 - 52710016 52710016 52710016 GCTAATAATTGCAGTTTACAGAATTAGAGATCAGGCAAAATTATTTCCAATCATCTTTTCTCTGA GCTAATAATTGCAGTTTACAGAATTAGAGATCCGGCAAAATTATTTCCAATCATCTTTTCTCTGA T G RB1CC1 Ensembl:ENSG00000023287 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1456710898 Functional Loss SNV dbSNP153 33..33 33 - - - 29026 RMVar_ID_29026 Human_SNP_ID_363659276 A-to-I Human chr8 - 53810485 53810485 53810485 CGCCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCACGCCAGGCCTTCTTTC CGCCTGCCTTGGCCTCCCAAAGTGCTGGGATTGCAGGCATGAGCCACCACGCCAGGCCTTCTTTC T C ATP6V1H Ensembl:ENSG00000047249 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956989182 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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 29027 RMVar_ID_29027 Human_SNP_ID_363677803 A-to-I Human chr8 + 53885480 53885480 53885480 CTAAAAAATACAAAAAATTAGCTGGGCGTATTAGCGGGCGTCTGTAGTACCAGCTACTCGGGAGG CTAAAAAATACAAAAAATTAGCTGGGCGTATTGGCGGGCGTCTGTAGTACCAGCTACTCGGGAGG A G RGS20 Ensembl:ENSG00000147509 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1163763571 Functional Loss SNV dbSNP153 33..33 33 - - - 29028 RMVar_ID_29028 Human_SNP_ID_363681060 A-to-I Human chr8 + 53900342 53900342 53900342 TTTTAAATTTTTTTTAGAGACGGGGTCTCACTATGTTGCCCAGGCTGGTCTCAAACTCCTGGACT TTTTAAATTTTTTTTAGAGACGGGGTCTCACTCTGTTGCCCAGGCTGGTCTCAAACTCCTGGACT A C RGS20 Ensembl:ENSG00000147509 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903311434 Functional Loss SNV dbSNP153 33..33 33 - - - 29029 RMVar_ID_29029 Human_SNP_ID_363681061 A-to-I Human chr8 + 53900342 53900342 53900342 TTTTAAATTTTTTTTAGAGACGGGGTCTCACTATGTTGCCCAGGCTGGTCTCAAACTCCTGGACT TTTTAAATTTTTTTTAGAGACGGGGTCTCACTGTGTTGCCCAGGCTGGTCTCAAACTCCTGGACT A G RGS20 Ensembl:ENSG00000147509 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903311434 Functional Loss SNV dbSNP153 33..33 33 - - - 29030 RMVar_ID_29030 Human_SNP_ID_363693921 A-to-I Human chr8 + 53953432 53953431 53953432 AGGGTCTGCTACTTGGGAGGCCAAGGAGAGAGAATCATATGAGCCTAGTAAGTCGAGGCTTCAGT AGGGTCTGCTACTTGGGAGGCCAAGGAGAGAG_ATCATATGAGCCTAGTAAGTCGAGGCTTCAGT GA G RGS20 Ensembl:ENSG00000147509 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1395867857 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_325932,RMVar_hsa_circ_252117,RMVar_hsa_circ_326525 29031 RMVar_ID_29031 Human_SNP_ID_363701695 A-to-I Human chr8 - 53984649 53984649 53984649 TCGATCTCCTGACCTCGTGATCCACCAGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAG TCGATCTCCTGACCTCGTGATCCACCAGCCTCTGCCTCCCAAAGTGCTGGGATTACAGGCATGAG T A TCEA1 Ensembl:ENSG00000187735 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs993946047 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115429,RMVar_hsa_circ_252122,RMVar_hsa_circ_279413,RMVar_hsa_circ_252120,RMVar_hsa_circ_339390,RMVar_hsa_circ_338199,RMVar_hsa_circ_271499,RMVar_hsa_circ_252125,RMVar_hsa_circ_280881,RMVar_hsa_circ_316564,RMVar_hsa_circ_252121,RMVar_hsa_circ_299121,RMVar_hsa_circ_252126,RMVar_hsa_circ_67128,RMVar_hsa_circ_297988,RMVar_hsa_circ_320224,RMVar_hsa_circ_296723,RMVar_hsa_circ_58148 29032 RMVar_ID_29032 Human_SNP_ID_363701696 A-to-I Human chr8 - 53984649 53984649 53984649 TCGATCTCCTGACCTCGTGATCCACCAGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAG TCGATCTCCTGACCTCGTGATCCACCAGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAG T C TCEA1 Ensembl:ENSG00000187735 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs993946047 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115429,RMVar_hsa_circ_252122,RMVar_hsa_circ_279413,RMVar_hsa_circ_252120,RMVar_hsa_circ_339390,RMVar_hsa_circ_338199,RMVar_hsa_circ_271499,RMVar_hsa_circ_252125,RMVar_hsa_circ_280881,RMVar_hsa_circ_316564,RMVar_hsa_circ_252121,RMVar_hsa_circ_299121,RMVar_hsa_circ_252126,RMVar_hsa_circ_67128,RMVar_hsa_circ_297988,RMVar_hsa_circ_320224,RMVar_hsa_circ_296723,RMVar_hsa_circ_58148 29033 RMVar_ID_29033 Human_SNP_ID_363701721 A-to-I Human chr8 - 53984735 53984735 53984735 GGGACTGCAGGCACCTGCCACCATGCCTGGTTAATTTTTTGTGTTTTTAATAGAGACGGGGTTTC GGGACTGCAGGCACCTGCCACCATGCCTGGTTGATTTTTTGTGTTTTTAATAGAGACGGGGTTTC T C TCEA1 Ensembl:ENSG00000187735 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1456844073 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115429,RMVar_hsa_circ_252122,RMVar_hsa_circ_279413,RMVar_hsa_circ_252120,RMVar_hsa_circ_339390,RMVar_hsa_circ_338199,RMVar_hsa_circ_271499,RMVar_hsa_circ_252125,RMVar_hsa_circ_280881,RMVar_hsa_circ_316564,RMVar_hsa_circ_252121,RMVar_hsa_circ_299121,RMVar_hsa_circ_252126,RMVar_hsa_circ_67128,RMVar_hsa_circ_297988,RMVar_hsa_circ_320224,RMVar_hsa_circ_296723,RMVar_hsa_circ_58148 29034 RMVar_ID_29034 Human_SNP_ID_363701898 A-to-I Human chr8 - 53985292 53985292 53985292 CATGACTAGGCCGGGCGCGGTGGCTCACGCCTATAATCCCAGCACTTTGAGAGGCCGAGACGGGT CATGACTAGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGAGAGGCCGAGACGGGT T C TCEA1 Ensembl:ENSG00000187735 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1424905031 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115429,RMVar_hsa_circ_252122,RMVar_hsa_circ_279413,RMVar_hsa_circ_252120,RMVar_hsa_circ_339390,RMVar_hsa_circ_338199,RMVar_hsa_circ_271499,RMVar_hsa_circ_252125,RMVar_hsa_circ_280881,RMVar_hsa_circ_316564,RMVar_hsa_circ_252121,RMVar_hsa_circ_299121,RMVar_hsa_circ_252126,RMVar_hsa_circ_67128,RMVar_hsa_circ_297988,RMVar_hsa_circ_320224,RMVar_hsa_circ_296723,RMVar_hsa_circ_58148 29035 RMVar_ID_29035 Human_SNP_ID_363703156 A-to-I Human chr8 - 53990314 53990313 53990314 TTTGGGGCCTGGCACGGTGGCTCAAGCACTTTAGGACGCCGAGGCGGAATTATCACTTGAGGTCA TTTGGGGCCTGGCACGGTGGCTCAAGCACTTT_GGACGCCGAGGCGGAATTATCACTTGAGGTCA CT C TCEA1 Ensembl:ENSG00000187735 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1482264405 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_16438475 RMVar_hsa_circ_7194,RMVar_hsa_circ_115429,RMVar_hsa_circ_279413,RMVar_hsa_circ_252120,RMVar_hsa_circ_338199,RMVar_hsa_circ_271499,RMVar_hsa_circ_252125,RMVar_hsa_circ_280881,RMVar_hsa_circ_316564,RMVar_hsa_circ_252121,RMVar_hsa_circ_299121,RMVar_hsa_circ_252126,RMVar_hsa_circ_67128,RMVar_hsa_circ_297988,RMVar_hsa_circ_320224,RMVar_hsa_circ_296723,RMVar_hsa_circ_252127,RMVar_hsa_circ_111919,RMVar_hsa_circ_345672 29036 RMVar_ID_29036 Human_SNP_ID_363720870 A-to-I Human chr8 - 54059889 54059889 54059889 TACATAGTTACTTAGAGACTGTCGCCCAGGTTAGAGTACAGTTGGTGATCATATCTCACTGCAGC TACATAGTTACTTAGAGACTGTCGCCCAGGTTTGAGTACAGTTGGTGATCATATCTCACTGCAGC T A LYPLA1 Ensembl:ENSG00000120992 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1048312412 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16439372 RMVar_hsa_circ_109038,RMVar_hsa_circ_88292,RMVar_hsa_circ_252132,RMVar_hsa_circ_327324,RMVar_hsa_circ_252134,RMVar_hsa_circ_295712,RMVar_hsa_circ_252136,RMVar_hsa_circ_252137,RMVar_hsa_circ_370766,RMVar_hsa_circ_37498,RMVar_hsa_circ_252139 29037 RMVar_ID_29037 Human_SNP_ID_363720871 A-to-I Human chr8 - 54059889 54059889 54059889 TACATAGTTACTTAGAGACTGTCGCCCAGGTTAGAGTACAGTTGGTGATCATATCTCACTGCAGC TACATAGTTACTTAGAGACTGTCGCCCAGGTTGGAGTACAGTTGGTGATCATATCTCACTGCAGC T C LYPLA1 Ensembl:ENSG00000120992 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1048312412 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16439372 RMVar_hsa_circ_109038,RMVar_hsa_circ_88292,RMVar_hsa_circ_252132,RMVar_hsa_circ_327324,RMVar_hsa_circ_252134,RMVar_hsa_circ_295712,RMVar_hsa_circ_252136,RMVar_hsa_circ_252137,RMVar_hsa_circ_370766,RMVar_hsa_circ_37498,RMVar_hsa_circ_252139 29038 RMVar_ID_29038 Human_SNP_ID_363721355 A-to-I Human chr8 - 54061699 54061699 54061699 AAGCTCACTGCAGCCTTGACCTCCTGAACTCAAGCGACCCTTCCACCTCATCCTCCTGAGTAGGC AAGCTCACTGCAGCCTTGACCTCCTGAACTCAGGCGACCCTTCCACCTCATCCTCCTGAGTAGGC T C LYPLA1 Ensembl:ENSG00000120992 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1485846018 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109038,RMVar_hsa_circ_88292,RMVar_hsa_circ_252132,RMVar_hsa_circ_327324,RMVar_hsa_circ_252134,RMVar_hsa_circ_295712,RMVar_hsa_circ_252136,RMVar_hsa_circ_252137,RMVar_hsa_circ_370766,RMVar_hsa_circ_37498,RMVar_hsa_circ_252139 29039 RMVar_ID_29039 Human_SNP_ID_363731834 A-to-I Human chr8 - 54099769 54099769 54099769 TGAGAGAAGAGAATCACTTGAACCTGGGAGGCAGAGGCTTCAGTGAGCCAAGATTGCACGACTGC TGAGAGAAGAGAATCACTTGAACCTGGGAGGCGGAGGCTTCAGTGAGCCAAGATTGCACGACTGC T C LYPLA1 Ensembl:ENSG00000120992 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1174624352 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94419,RMVar_hsa_circ_252142 29040 RMVar_ID_29040 Human_SNP_ID_363835531 A-to-I Human chr8 + 54523270 54523270 54523270 TCCAAAATTTAGGACTTGATAATAGAGCCGCCACTTGTTCATCCACTGCACATCATCCAAAAAGA TCCAAAATTTAGGACTTGATAATAGAGCCGCCGCTTGTTCATCCACTGCACATCATCCAAAAAGA A G RP1 Ensembl:ENSG00000104237 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1427956781 Functional Loss SNV dbSNP153 33..33 33 - - - 29041 RMVar_ID_29041 Human_SNP_ID_364068745 A-to-I Human chr8 - 55449743 55449743 55449743 TGGTTCATGTTAGACAAGACCAAGCACCAGCTACGCTACTACGACCACCGTGTGGACACTGAGTG TGGTTCATGTTAGACAAGACCAAGCACCAGCTGCGCTACTACGACCACCGTGTGGACACTGAGTG T C SBF1P1 Ensembl:ENSG00000248522 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1414989963 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17320395 29042 RMVar_ID_29042 Human_SNP_ID_364147469 A-to-I Human chr8 - 55745813 55745813 55745813 TCACGCCTGTAATCCTAACACTTTGGGAAACTAAGGTTGGAGGATTGCTTGAACCTGGGAGGTTG TCACGCCTGTAATCCTAACACTTTGGGAAACTGAGGTTGGAGGATTGCTTGAACCTGGGAGGTTG T C TMEM68 Ensembl:ENSG00000167904 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1271763781 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63574,RMVar_hsa_circ_362093,RMVar_hsa_circ_252154,RMVar_hsa_circ_369224,RMVar_hsa_circ_352793,RMVar_hsa_circ_68580,RMVar_hsa_circ_252156 29043 RMVar_ID_29043 Human_SNP_ID_364147598 A-to-I Human chr8 - 55746253 55746253 55746253 GGAGTGCAGTGGTGTGATCTTGGTTCACTGCAACCTCTGCCTCCTGGTCTTAAACAATCCTCCCA GGAGTGCAGTGGTGTGATCTTGGTTCACTGCAGCCTCTGCCTCCTGGTCTTAAACAATCCTCCCA T C TMEM68 Ensembl:ENSG00000167904 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1182499676 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63574,RMVar_hsa_circ_362093,RMVar_hsa_circ_252154,RMVar_hsa_circ_369224,RMVar_hsa_circ_352793,RMVar_hsa_circ_68580,RMVar_hsa_circ_252156 29044 RMVar_ID_29044 Human_SNP_ID_364149148 A-to-I Human chr8 - 55752930 55752930 55752930 GCTCAGAAGATTGAAACCACCCTGGGCAACATAGCAAGACCTCGTTTCTGCTAAAAATAAAAATA GCTCAGAAGATTGAAACCACCCTGGGCAACATGGCAAGACCTCGTTTCTGCTAAAAATAAAAATA T C TMEM68 Ensembl:ENSG00000167904 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1206926120 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_252154,RMVar_hsa_circ_369224,RMVar_hsa_circ_352793,RMVar_hsa_circ_68580,RMVar_hsa_circ_252157,RMVar_hsa_circ_294568,RMVar_hsa_circ_252156,RMVar_hsa_circ_301554,RMVar_hsa_circ_252158 29045 RMVar_ID_29045 Human_SNP_ID_364149163 A-to-I Human chr8 - 55753019 55753019 55753019 CTCAGCACAAGAGAGATTTTAGGGTGGGTGCCATGGCTCACACCTGTAATTCCAGCACTTGGTGA CTCAGCACAAGAGAGATTTTAGGGTGGGTGCCGTGGCTCACACCTGTAATTCCAGCACTTGGTGA T C TMEM68 Ensembl:ENSG00000167904 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs182436855 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_252154,RMVar_hsa_circ_369224,RMVar_hsa_circ_352793,RMVar_hsa_circ_68580,RMVar_hsa_circ_252157,RMVar_hsa_circ_294568,RMVar_hsa_circ_252156,RMVar_hsa_circ_301554,RMVar_hsa_circ_252158 29046 RMVar_ID_29046 Human_SNP_ID_364154130 A-to-I Human chr8 - 55771495 55771495 55771495 CTCCTACCTCAGCCCCCCGAGTAGCTGGGGCTACAGGCATGCCACCATGCCTGCCTAATTTTGTG CTCCTACCTCAGCCCCCCGAGTAGCTGGGGCTGCAGGCATGCCACCATGCCTGCCTAATTTTGTG T C TMEM68 Ensembl:ENSG00000167904 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1448100941 Functional Loss SNV dbSNP153 33..33 33 - - - 29047 RMVar_ID_29047 Human_SNP_ID_364154134 A-to-I Human chr8 - 55771505 55771505 55771505 TCAAGCAATCCTCCTACCTCAGCCCCCCGAGTAGCTGGGGCTACAGGCATGCCACCATGCCTGCC TCAAGCAATCCTCCTACCTCAGCCCCCCGAGTGGCTGGGGCTACAGGCATGCCACCATGCCTGCC T C TMEM68 Ensembl:ENSG00000167904 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs528531364 Functional Loss SNV dbSNP153 33..33 33 - - - 29048 RMVar_ID_29048 Human_SNP_ID_364155192 A-to-I Human chr8 + 55775133 55775133 55775133 AAAATTAGCCAGCTGTGGTGGCACATGCTTGTAGTCCCAGCTACTCTGGAGGCTTGGGCCAGATG AAAATTAGCCAGCTGTGGTGGCACATGCTTGTGGTCCCAGCTACTCTGGAGGCTTGGGCCAGATG A G TGS1 Ensembl:ENSG00000137574 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1490893985 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117781,RMVar_hsa_circ_252160 29049 RMVar_ID_29049 Human_SNP_ID_364168544 A-to-I Human chr8 + 55825025 55825025 55825025 CTCACTGCAGGTTCAGCCTTCTGAGTTCAAGCAATCCTTCTGTCTCAGTCTCCTCAGTAGCTGGG CTCACTGCAGGTTCAGCCTTCTGAGTTCAAGCCATCCTTCTGTCTCAGTCTCCTCAGTAGCTGGG A C TGS1 Ensembl:ENSG00000137574 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1273779217 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27366744 RMVar_hsa_circ_117047,RMVar_hsa_circ_252161,RMVar_hsa_circ_79205,RMVar_hsa_circ_252180,RMVar_hsa_circ_105271,RMVar_hsa_circ_252182 29050 RMVar_ID_29050 Human_SNP_ID_364168943 A-to-I Human chr8 + 55826643 55826643 55826643 CAGCATAGTGAAACCCCGCCTCTACTAAAAATACAAAAATTAGCCAGGCATGGTGGCACATACAT CAGCATAGTGAAACCCCGCCTCTACTAAAAATGCAAAAATTAGCCAGGCATGGTGGCACATACAT A G RF00017-4497,RF00017-4706 RNACentral:URS0000961FEC,RNACentral:URS000095B12E SRP RNA,SRP RNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1283906813 Functional Loss SNV dbSNP153 33..33 33 - - - 29051 RMVar_ID_29051 Human_SNP_ID_364169174 A-to-I Human chr8 + 55827365 55827365 55827365 GTTTGTTTGTTTTTGAGACTGAGCCTCACTCTATCGCCCAGGCTGGAGTGCAGTGGCGCGATCTC GTTTGTTTGTTTTTGAGACTGAGCCTCACTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCGATCTC A G RF00017-4497,RF00017-4706 RNACentral:URS0000961FEC,RNACentral:URS000095B12E SRP RNA,SRP RNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs976608019 Functional Loss SNV dbSNP153 33..33 33 - - - 29052 RMVar_ID_29052 Human_SNP_ID_364169175 A-to-I Human chr8 + 55827365 55827365 55827365 GTTTGTTTGTTTTTGAGACTGAGCCTCACTCTATCGCCCAGGCTGGAGTGCAGTGGCGCGATCTC GTTTGTTTGTTTTTGAGACTGAGCCTCACTCTTTCGCCCAGGCTGGAGTGCAGTGGCGCGATCTC A T RF00017-4497,RF00017-4706 RNACentral:URS0000961FEC,RNACentral:URS000095B12E SRP RNA,SRP RNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs976608019 Functional Loss SNV dbSNP153 33..33 33 - - - 29053 RMVar_ID_29053 Human_SNP_ID_364185289 A-to-I Human chr8 + 55890267 55890267 55890267 CCAGGAGATTGAGGCTGCAGTGAGCAATGATTACACCACCACACTCCATCCTGGGTGACAGAGCG CCAGGAGATTGAGGCTGCAGTGAGCAATGATTGCACCACCACACTCCATCCTGGGTGACAGAGCG A G LYN Ensembl:ENSG00000254087 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs552015820 Functional Loss SNV dbSNP153 33..33 33 - - - 29054 RMVar_ID_29054 Human_SNP_ID_364185443 A-to-I Human chr8 + 55890867 55890867 55890867 CTCCCACCTCAGCCTCTTGAGTAGCTGAGACTACAGGTGCATGCCACCATGCCTGGCTAGTTTTT CTCCCACCTCAGCCTCTTGAGTAGCTGAGACTGCAGGTGCATGCCACCATGCCTGGCTAGTTTTT A G LYN Ensembl:ENSG00000254087 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1360389783 Functional Loss SNV dbSNP153 33..33 33 - - - 29055 RMVar_ID_29055 Human_SNP_ID_364185521 A-to-I Human chr8 + 55891231 55891231 55891231 AAAATTAGTCGAACATGGTGGTGCATGCCTGTAATCCTGGCTACTTGGGAGGCTGAGGCAGAAGA AAAATTAGTCGAACATGGTGGTGCATGCCTGTGATCCTGGCTACTTGGGAGGCTGAGGCAGAAGA A G LYN Ensembl:ENSG00000254087 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1180814809 Functional Loss SNV dbSNP153 33..33 33 - - - 29056 RMVar_ID_29056 Human_SNP_ID_364186986 A-to-I Human chr8 + 55897721 55897721 55897721 ATCACTTGAGCGCAGAAGTTTGAGACCATCCTAGGCAACATAGTGAGACCTCATCTCTATAGGAA ATCACTTGAGCGCAGAAGTTTGAGACCATCCTGGGCAACATAGTGAGACCTCATCTCTATAGGAA A G LYN Ensembl:ENSG00000254087 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1164531974 Functional Loss SNV dbSNP153 33..33 33 - - - 29057 RMVar_ID_29057 Human_SNP_ID_364186994 A-to-I Human chr8 + 55897766 55897766 55897766 AGACCTCATCTCTATAGGAAATTAAAAAAATTAGCCAAGAGTGGTGGCATGGGCCTGTATTCCCA AGACCTCATCTCTATAGGAAATTAAAAAAATTGGCCAAGAGTGGTGGCATGGGCCTGTATTCCCA A G LYN Ensembl:ENSG00000254087 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1489828988 Functional Loss SNV dbSNP153 33..33 33 - - - 29058 RMVar_ID_29058 Human_SNP_ID_364188739 A-to-I Human chr8 + 55905201 55905201 55905201 GGGAGGCTGAGGCAGGCGGATCACCTGAGGTCAGGAGTTCAAGGCCAGCCTGGCCAACATGGTGA GGGAGGCTGAGGCAGGCGGATCACCTGAGGTCGGGAGTTCAAGGCCAGCCTGGCCAACATGGTGA A G LYN Ensembl:ENSG00000254087 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs531094589 Functional Loss SNV dbSNP153 33..33 33 - - - 29059 RMVar_ID_29059 Human_SNP_ID_364189070 A-to-I Human chr8 + 55906518 55906518 55906518 AGCTGGGATTACATGTGCCCACCACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGACAGAGT AGCTGGGATTACATGTGCCCACCACCACGCCCCGCTAATTTTTGTATTTTTAGTAGAGACAGAGT A C LYN Ensembl:ENSG00000254087 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs989199901 Functional Loss SNV dbSNP153 33..33 33 - - - 29060 RMVar_ID_29060 Human_SNP_ID_364192179 A-to-I Human chr8 + 55917384 55917384 55917384 ATTTTAGTTTTTTGTAGAGATAGGGTCTTGCTATGTTGCCCAGGCTGGTCTTGAACTTTTGGACT ATTTTAGTTTTTTGTAGAGATAGGGTCTTGCTGTGTTGCCCAGGCTGGTCTTGAACTTTTGGACT A G LYN Ensembl:ENSG00000254087 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs958909292 Functional Loss SNV dbSNP153 33..33 33 - - - 29061 RMVar_ID_29061 Human_SNP_ID_364198288 A-to-I Human chr8 + 55943455 55943455 55943455 AAAATTAGCCGGGTGTGGTGGTGCGTGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGAAGAAGA AAAATTAGCCGGGTGTGGTGGTGCGTGCCTGTGGTCCCAGCTACTTGGGAGGCTGAGGAAGAAGA A G LYN Ensembl:ENSG00000254087 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1007556875 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_252185,RMVar_hsa_circ_316980,RMVar_hsa_circ_326176,RMVar_hsa_circ_367797,RMVar_hsa_circ_319065,RMVar_hsa_circ_295356,RMVar_hsa_circ_252183,RMVar_hsa_circ_252184 29062 RMVar_ID_29062 Human_SNP_ID_364211513 A-to-I Human chr8 + 56000648 56000648 56000648 TACTTGGGAGGCTGAGGCAGGAGAATCACTTCAACCTGGGAAGCACAGGTTGCAGTGAGCCGAGA TACTTGGGAGGCTGAGGCAGGAGAATCACTTCTACCTGGGAAGCACAGGTTGCAGTGAGCCGAGA A T LYN Ensembl:ENSG00000254087 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1484057530 Functional Loss SNV dbSNP153 33..33 33 - - - 29063 RMVar_ID_29063 Human_SNP_ID_364212283 A-to-I Human chr8 + 56003600 56003600 56003600 TGAGGCAGAGAATCGCTTGAATGCTTGAACCCAGGAGACAGAAGTTGCAGTGAGCCGAGATGCGC TGAGGCAGAGAATCGCTTGAATGCTTGAACCCGGGAGACAGAAGTTGCAGTGAGCCGAGATGCGC A G LYN Ensembl:ENSG00000254087 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1191452615 Functional Loss SNV dbSNP153 33..33 33 - - - 29064 RMVar_ID_29064 Human_SNP_ID_364214601 A-to-I Human chr8 + 56013436 56013436 56013436 GGAACTACAGGCACACACCATCTCGCCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCA GGAACTACAGGCACACACCATCTCGCCTGGCTTATTTTTGTATTTTTAGTAGAGATGGGGTTTCA A T LYN Ensembl:ENSG00000254087 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1187725753 Functional Loss SNV dbSNP153 33..33 33 - - - 29065 RMVar_ID_29065 Human_SNP_ID_364223708 A-to-I Human chr8 - 56050649 56050649 56050649 CAGGTACGGGAAAAACACTCTTGGCACGAGCCATTGCTAGCCAGCTGGACTGCAATTTCTTAAAG CAGGTACGGGAAAAACACTCTTGGCACGAGCCGTTGCTAGCCAGCTGGACTGCAATTTCTTAAAG T C AC046176.1 Ensembl:ENSG00000236814 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879185840 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22012957,Human_RBP_ID_22410643 Human_miRNA_ID_1876936,Human_miRNA_ID_1879943 29066 RMVar_ID_29066 Human_SNP_ID_364224271 A-to-I Human chr8 + 56052988 56052985 56052988 CGTTCCCACAGGAGTCCTTTTGTGATTATTACAACTACTAGTCCATTCCTCCAGATCCCAAAGTG CGTTCCCACAGGAGTCCTTTTGTGATTATT___ACTACTAGTCCATTCCTCCAGATCCCAAAGTG TACA T RF00017-4497,RF00017-071,RF00017-4513 RNACentral:URS0000961FEC,RNACentral:URS00009310A4,RNACentral:URS000090EECB SRP RNA,SRP RNA,SRP RNA intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1305063383 Functional Loss DEL dbSNP153 31..33 33 - - - 29067 RMVar_ID_29067 Human_SNP_ID_364227690 A-to-I Human chr8 - 56066845 56066845 56066845 TGACTGCAACCTCTGCCTCCCGAGTTCAAGCAATTCTCCTGCCTCATCCTCCCACGTAGCTGGGA TGACTGCAACCTCTGCCTCCCGAGTTCAAGCATTTCTCCTGCCTCATCCTCCCACGTAGCTGGGA T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1369442891 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16441860 29068 RMVar_ID_29068 Human_SNP_ID_364227691 A-to-I Human chr8 - 56066845 56066845 56066845 TGACTGCAACCTCTGCCTCCCGAGTTCAAGCAATTCTCCTGCCTCATCCTCCCACGTAGCTGGGA TGACTGCAACCTCTGCCTCCCGAGTTCAAGCAGTTCTCCTGCCTCATCCTCCCACGTAGCTGGGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1369442891 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16441860 29069 RMVar_ID_29069 Human_SNP_ID_364227692 A-to-I Human chr8 - 56066846 56066846 56066846 CTGACTGCAACCTCTGCCTCCCGAGTTCAAGCAATTCTCCTGCCTCATCCTCCCACGTAGCTGGG CTGACTGCAACCTCTGCCTCCCGAGTTCAAGCGATTCTCCTGCCTCATCCTCCCACGTAGCTGGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1291306636 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16441860 29070 RMVar_ID_29070 Human_SNP_ID_364228202 A-to-I Human chr8 - 56068341 56068341 56068341 TAGAGATGGGGTTATGCCATTTTGGCCAGGCTAGTCTCGAACTCCTGAGCTCAGGTGATACACAC TAGAGATGGGGTTATGCCATTTTGGCCAGGCTGGTCTCGAACTCCTGAGCTCAGGTGATACACAC T C RPS20 Ensembl:ENSG00000008988 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs889153327 Functional Loss SNV dbSNP153 33..33 33 - - - 29071 RMVar_ID_29071 Human_SNP_ID_364228471 A-to-I Human chr8 - 56068927 56068927 56068927 GGGCGTGGCAGTGCGTGCCTGTGGTCCCAGCCACTTGGGAGGCTGAGGCATGAGAATTACTTGAA GGGCGTGGCAGTGCGTGCCTGTGGTCCCAGCCCCTTGGGAGGCTGAGGCATGAGAATTACTTGAA T G RPS20 Ensembl:ENSG00000008988 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs13269579 Functional Loss SNV dbSNP153 33..33 33 - - - 29072 RMVar_ID_29072 Human_SNP_ID_364228983 A-to-I Human chr8 - 56070533 56070533 56070533 TGGGGTCTTGCCATGTTGCCCAGGCTGGTCTCAAACTCCTATGCTCAGGCGATCCACCCTCCTCG TGGGGTCTTGCCATGTTGCCCAGGCTGGTCTCGAACTCCTATGCTCAGGCGATCCACCCTCCTCG T C RPS20 Ensembl:ENSG00000008988 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1331329185 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96015,RMVar_hsa_circ_252195 29073 RMVar_ID_29073 Human_SNP_ID_364364886 A-to-I Human chr8 + 56588507 56588507 56588507 CTCTAAGGCCTACCACCTTCAGAAGTCGACCTATGGCAAATGTGGCTACACTGCCAAGCGCAAGA CTCTAAGGCCTACCACCTTCAGAAGTCGACCTGTGGCAAATGTGGCTACACTGCCAAGCGCAAGA A G RPL37P6 Ensembl:ENSG00000241431 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879168318 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5629547 29074 RMVar_ID_29074 Human_SNP_ID_364364900 A-to-I Human chr8 + 56588557 56588557 56588557 CTGCCAAGCGCAAGAGAAAGTATAACTGGAGTACCAAGGCTAAAAGACGAAATACCACCAGAACT CTGCCAAGCGCAAGAGAAAGTATAACTGGAGTGCCAAGGCTAAAAGACGAAATACCACCAGAACT A G RPL37P6 Ensembl:ENSG00000241431 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879038987 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5629547 29075 RMVar_ID_29075 Human_SNP_ID_364364908 A-to-I Human chr8 + 56588584 56588584 56588584 GGAGTACCAAGGCTAAAAGACGAAATACCACCAGAACTGGTCAAATGAGGCACCTAAAAATTGTA GGAGTACCAAGGCTAAAAGACGAAATACCACCGGAACTGGTCAAATGAGGCACCTAAAAATTGTA A G RPL37P6 Ensembl:ENSG00000241431 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878915350 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5629547 Human_miRNA_ID_1896336,Human_miRNA_ID_1902309 29076 RMVar_ID_29076 Human_SNP_ID_364364912 A-to-I Human chr8 + 56588594 56588594 56588594 GGCTAAAAGACGAAATACCACCAGAACTGGTCAAATGAGGCACCTAAAAATTGTATACCATAGAT GGCTAAAAGACGAAATACCACCAGAACTGGTCGAATGAGGCACCTAAAAATTGTATACCATAGAT A G RPL37P6 Ensembl:ENSG00000241431 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879087265 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5629547 Human_miRNA_ID_1896336,Human_miRNA_ID_1902309 29077 RMVar_ID_29077 Human_SNP_ID_364364919 A-to-I Human chr8 + 56588621 56588621 56588621 TGGTCAAATGAGGCACCTAAAAATTGTATACCATAGATTCAGGCATGGATTCCGTGAAGGAACAA TGGTCAAATGAGGCACCTAAAAATTGTATACCGTAGATTCAGGCATGGATTCCGTGAAGGAACAA A G RPL37P6 Ensembl:ENSG00000241431 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878963294 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5629547 Human_miRNA_ID_1895023 29078 RMVar_ID_29078 Human_SNP_ID_364833536 A-to-I Human chr8 + 58428543 58428543 58428543 TCCTAGAATTTTGTCCCTTGTCCTCTGTGCTTATCTAAGTCCTAATGTCCTAAATCCTTTTAAGG TCCTAGAATTTTGTCCCTTGTCCTCTGTGCTTGTCTAAGTCCTAATGTCCTAAATCCTTTTAAGG A G UBXN2B Ensembl:ENSG00000215114 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1189711907 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103347,RMVar_hsa_circ_376124,RMVar_hsa_circ_252210,RMVar_hsa_circ_252211 29079 RMVar_ID_29079 Human_SNP_ID_364833537 A-to-I Human chr8 + 58428543 58428543 58428543 TCCTAGAATTTTGTCCCTTGTCCTCTGTGCTTATCTAAGTCCTAATGTCCTAAATCCTTTTAAGG TCCTAGAATTTTGTCCCTTGTCCTCTGTGCTTTTCTAAGTCCTAATGTCCTAAATCCTTTTAAGG A T UBXN2B Ensembl:ENSG00000215114 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1189711907 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103347,RMVar_hsa_circ_376124,RMVar_hsa_circ_252210,RMVar_hsa_circ_252211 29080 RMVar_ID_29080 Human_SNP_ID_364834162 A-to-I Human chr8 + 58431251 58431251 58431251 CATGCCTGTAATCCTAGCACTTTGGGAGGCCGAAGCAGGCAGATCACAGTTCAAGACCAGCCTGG CATGCCTGTAATCCTAGCACTTTGGGAGGCCGCAGCAGGCAGATCACAGTTCAAGACCAGCCTGG A C UBXN2B Ensembl:ENSG00000215114 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1021858527 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7561,RMVar_hsa_circ_376124,RMVar_hsa_circ_252211,RMVar_hsa_circ_291070,RMVar_hsa_circ_252213 29081 RMVar_ID_29081 Human_SNP_ID_364834529 A-to-I Human chr8 + 58432656 58432656 58432656 CGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACGAGCATGAGCCACCTCTATACAGCTTTTATA CGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTCCGAGCATGAGCCACCTCTATACAGCTTTTATA A C UBXN2B Ensembl:ENSG00000215114 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027332207 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7561,RMVar_hsa_circ_376124,RMVar_hsa_circ_252211,RMVar_hsa_circ_291070,RMVar_hsa_circ_252213 29082 RMVar_ID_29082 Human_SNP_ID_364873043 A-to-I Human chr8 - 58591766 58591766 58591766 AGGTTGTTTTGAGGCCGGGCACAGTTACTCACACCTGTAATCCCAGTATTTTGGGAGGCCGAAGG AGGTTGTTTTGAGGCCGGGCACAGTTACTCACGCCTGTAATCCCAGTATTTTGGGAGGCCGAAGG T C NSMAF Ensembl:ENSG00000035681 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1406790236 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16444079 RMVar_hsa_circ_58081,RMVar_hsa_circ_48015,RMVar_hsa_circ_37644,RMVar_hsa_circ_40831,RMVar_hsa_circ_267790,RMVar_hsa_circ_363508,RMVar_hsa_circ_252220 29083 RMVar_ID_29083 Human_SNP_ID_131536495 A-to-I Human chr3 + 45536323 45536323 45536323 TTTATTTTTTTGTAGAGACTAGGGCCTAGGCTAGTCTTGAACTCCTGGGCTTAAGTGATACCTCC TTTATTTTTTTGTAGAGACTAGGGCCTAGGCTGGTCTTGAACTCCTGGGCTTAAGTGATACCTCC A G LARS2 Ensembl:ENSG00000011376 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946687875 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124359,RMVar_hsa_circ_89849,RMVar_hsa_circ_217402,RMVar_hsa_circ_217403,RMVar_hsa_circ_81698,RMVar_hsa_circ_217410,RMVar_hsa_circ_217417,RMVar_hsa_circ_117023,RMVar_hsa_circ_102986,RMVar_hsa_circ_217426,RMVar_hsa_circ_80218,RMVar_hsa_circ_217427 29084 RMVar_ID_29084 Human_SNP_ID_131554406 A-to-I Human chr3 + 45612184 45612184 45612184 TTAGCTCACTGTAGCCTTGGCTTCCTGGGCTCAAGCAATCCTCCCATCCCAGCCCCCCGAATAAC TTAGCTCACTGTAGCCTTGGCTTCCTGGGCTCTAGCAATCCTCCCATCCCAGCCCCCCGAATAAC A T LIMD1 Ensembl:ENSG00000144791 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs564229736 Functional Loss SNV dbSNP153 33..33 33 - - - 29085 RMVar_ID_29085 Human_SNP_ID_131555230 A-to-I Human chr3 + 45615576 45615576 45615576 CTGGGAAGTTGAGGCTGCCTGGGCCACATGGCAAAACCCCATCTCTACTAAAAATGCGAAAAATT CTGGGAAGTTGAGGCTGCCTGGGCCACATGGCGAAACCCCATCTCTACTAAAAATGCGAAAAATT A G LIMD1 Ensembl:ENSG00000144791 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs113322790 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_324991,RMVar_hsa_circ_346287 29086 RMVar_ID_29086 Human_SNP_ID_131555231 A-to-I Human chr3 + 45615576 45615576 45615576 CTGGGAAGTTGAGGCTGCCTGGGCCACATGGCAAAACCCCATCTCTACTAAAAATGCGAAAAATT CTGGGAAGTTGAGGCTGCCTGGGCCACATGGCTAAACCCCATCTCTACTAAAAATGCGAAAAATT A T LIMD1 Ensembl:ENSG00000144791 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs113322790 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_324991,RMVar_hsa_circ_346287 29087 RMVar_ID_29087 Human_SNP_ID_131557529 A-to-I Human chr3 + 45625351 45625351 45625351 TATGGAGCCTAAACAAACAAGAAATGCCGAGTACCTCACACTCAGTAGATGCCGAATAAGCATGG TATGGAGCCTAAACAAACAAGAAATGCCGAGTGCCTCACACTCAGTAGATGCCGAATAAGCATGG A G LIMD1 Ensembl:ENSG00000144791 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs367712712 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_324991,RMVar_hsa_circ_346287 29088 RMVar_ID_29088 Human_SNP_ID_131570494 A-to-I Human chr3 + 45680344 45680340 45680344 TTCTTTTCTTTTTTTTTTTGAGACAGGGCCTCACTCTGTTGCCCAGGCTGGAGTGCAGTGGCGCG TTCTTTTCTTTTTTTTTTTGAGACAGGGC____CTCTGTTGCCCAGGCTGGAGTGCAGTGGCGCG CCTCA C LIMD1 Ensembl:ENSG00000144791 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,31158229,31158229,31158229 RNA-Seq:(High) rs566830328 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_106099,RMVar_hsa_circ_217433 29089 RMVar_ID_29089 Human_SNP_ID_131570496 A-to-I Human chr3 + 45680344 45680344 45680344 TTCTTTTCTTTTTTTTTTTGAGACAGGGCCTCACTCTGTTGCCCAGGCTGGAGTGCAGTGGCGCG TTCTTTTCTTTTTTTTTTTGAGACAGGGCCTCGCTCTGTTGCCCAGGCTGGAGTGCAGTGGCGCG A G LIMD1 Ensembl:ENSG00000144791 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,31158229,31158229,31158229 RNA-Seq:(High) rs1420439251 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106099,RMVar_hsa_circ_217433 29090 RMVar_ID_29090 Human_SNP_ID_131570504 A-to-I Human chr3 + 45680368 45680368 45680368 AGGGCCTCACTCTGTTGCCCAGGCTGGAGTGCAGTGGCGCGATCTCAGCTCACTGCAGCCTCCAC AGGGCCTCACTCTGTTGCCCAGGCTGGAGTGCGGTGGCGCGATCTCAGCTCACTGCAGCCTCCAC A G LIMD1 Ensembl:ENSG00000144791 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,31158229,31158229 RNA-Seq:(High) rs1260160185 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106099,RMVar_hsa_circ_217433 29091 RMVar_ID_29091 Human_SNP_ID_131570510 A-to-I Human chr3 + 45680377 45680377 45680377 CTCTGTTGCCCAGGCTGGAGTGCAGTGGCGCGATCTCAGCTCACTGCAGCCTCCACCTACTGGGC CTCTGTTGCCCAGGCTGGAGTGCAGTGGCGCGGTCTCAGCTCACTGCAGCCTCCACCTACTGGGC A G LIMD1 Ensembl:ENSG00000144791 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,24183664,29129909,29796672,31158229,31158229,31158229 RNA-Seq:(High) rs1326185591 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106099,RMVar_hsa_circ_217433 29092 RMVar_ID_29092 Human_SNP_ID_131570511 A-to-I Human chr3 + 45680382 45680382 45680382 TTGCCCAGGCTGGAGTGCAGTGGCGCGATCTCAGCTCACTGCAGCCTCCACCTACTGGGCTCAAG TTGCCCAGGCTGGAGTGCAGTGGCGCGATCTCGGCTCACTGCAGCCTCCACCTACTGGGCTCAAG A G LIMD1 Ensembl:ENSG00000144791 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1406403678 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106099,RMVar_hsa_circ_217433 29093 RMVar_ID_29093 Human_SNP_ID_131570515 A-to-I Human chr3 + 45680399 45680399 45680399 CAGTGGCGCGATCTCAGCTCACTGCAGCCTCCACCTACTGGGCTCAAGTGATCCTCCCACCTCAG CAGTGGCGCGATCTCAGCTCACTGCAGCCTCCGCCTACTGGGCTCAAGTGATCCTCCCACCTCAG A G LIMD1 Ensembl:ENSG00000144791 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 31158229,32596459 RNA-Seq:(High) rs1421162603 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106099,RMVar_hsa_circ_217433 29094 RMVar_ID_29094 Human_SNP_ID_131570520 A-to-I Human chr3 + 45680425 45680425 45680425 GCCTCCACCTACTGGGCTCAAGTGATCCTCCCACCTCAGCCTCCCGAGTAGCCGGGACCACAGGC GCCTCCACCTACTGGGCTCAAGTGATCCTCCCGCCTCAGCCTCCCGAGTAGCCGGGACCACAGGC A G LIMD1 Ensembl:ENSG00000144791 Protein coding 3'UTR GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,29796672,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs1199507975 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106099,RMVar_hsa_circ_217433 29095 RMVar_ID_29095 Human_SNP_ID_131570522 A-to-I Human chr3 + 45680430 45680430 45680430 CACCTACTGGGCTCAAGTGATCCTCCCACCTCAGCCTCCCGAGTAGCCGGGACCACAGGCGTGTA CACCTACTGGGCTCAAGTGATCCTCCCACCTCGGCCTCCCGAGTAGCCGGGACCACAGGCGTGTA A G LIMD1 Ensembl:ENSG00000144791 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1261160930 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106099,RMVar_hsa_circ_217433 29096 RMVar_ID_29096 Human_SNP_ID_131570537 A-to-I Human chr3 + 45680482 45680482 45680482 CCACAGGCGTGTATGACTGGCTACGCCTGGCTAATTTTTGTATTTTTAATAGAGACGAGTTTCAC CCACAGGCGTGTATGACTGGCTACGCCTGGCTTATTTTTGTATTTTTAATAGAGACGAGTTTCAC A T LIMD1 Ensembl:ENSG00000144791 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1406174174 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14833726 RMVar_hsa_circ_106099,RMVar_hsa_circ_217433 29097 RMVar_ID_29097 Human_SNP_ID_131570539 A-to-I Human chr3 + 45680497 45680497 45680497 ACTGGCTACGCCTGGCTAATTTTTGTATTTTTAATAGAGACGAGTTTCACCATGTTGCCCAGGAT ACTGGCTACGCCTGGCTAATTTTTGTATTTTTGATAGAGACGAGTTTCACCATGTTGCCCAGGAT A G LIMD1 Ensembl:ENSG00000144791 Protein coding 3'UTR GSE38233;GSE100210;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,29129909,31158229,31158229,31158229,31158229,31158229,32596459,32596459,32596459 RNA-Seq:(High) rs1475053982 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14833726 RMVar_hsa_circ_106099,RMVar_hsa_circ_217433 29098 RMVar_ID_29098 Human_SNP_ID_131570541 A-to-I Human chr3 + 45680500 45680500 45680500 GGCTACGCCTGGCTAATTTTTGTATTTTTAATAGAGACGAGTTTCACCATGTTGCCCAGGATGGT GGCTACGCCTGGCTAATTTTTGTATTTTTAATGGAGACGAGTTTCACCATGTTGCCCAGGATGGT A G LIMD1 Ensembl:ENSG00000144791 Protein coding 3'UTR GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,29796672,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs1018293152 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14833726 RMVar_hsa_circ_106099,RMVar_hsa_circ_217433 29099 RMVar_ID_29099 Human_SNP_ID_131570548 A-to-I Human chr3 + 45680537 45680537 45680537 CGAGTTTCACCATGTTGCCCAGGATGGTCTGGAACTCCTGGGCTCAAGTGATCTGCCCACTTCCG CGAGTTTCACCATGTTGCCCAGGATGGTCTGGCACTCCTGGGCTCAAGTGATCTGCCCACTTCCG A C LIMD1 Ensembl:ENSG00000144791 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1052411524 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17573585 Human_miRNA_ID_1605382,Human_miRNA_ID_1679630,Human_miRNA_ID_2992162 RMVar_hsa_circ_106099,RMVar_hsa_circ_217433 29100 RMVar_ID_29100 Human_SNP_ID_131570550 A-to-I Human chr3 + 45680550 45680550 45680550 GTTGCCCAGGATGGTCTGGAACTCCTGGGCTCAAGTGATCTGCCCACTTCCGCCTCCCAAAGTGT GTTGCCCAGGATGGTCTGGAACTCCTGGGCTCGAGTGATCTGCCCACTTCCGCCTCCCAAAGTGT A G LIMD1 Ensembl:ENSG00000144791 Protein coding 3'UTR GSE47997;GSE38233;GSE38233;GSE100210;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;cultured B-cells;HepG2 cell line;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,24183664,29129909,29129909,31158229,31158229,31158229,31158229,31158229,32596459,32596459 RNA-Seq:(High) rs1391937260 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17573585 RMVar_hsa_circ_106099,RMVar_hsa_circ_217433 29101 RMVar_ID_29101 Human_SNP_ID_131570568 A-to-I Human chr3 + 45680608 45680608 45680608 AAAGTGTTGGGATTATGGCCATTAGCCACTGTACCTGGCACAATTTTTTTTTGTACCCTCCTTTA AAAGTGTTGGGATTATGGCCATTAGCCACTGTGCCTGGCACAATTTTTTTTTGTACCCTCCTTTA A G LIMD1 Ensembl:ENSG00000144791 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1239473827 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23189287,Human_RBP_ID_26512095 Human_miRNA_ID_1803756 RMVar_hsa_circ_106099,RMVar_hsa_circ_217433 29102 RMVar_ID_29102 Human_SNP_ID_131570609 A-to-I Human chr3 + 45680755 45680755 45680755 CTGTAATCCCAGGCGCCGTGGCTCACGCCTGTAATCCCAGCACTTTGAGAGGCTGAGGCGGGTGG CTGTAATCCCAGGCGCCGTGGCTCACGCCTGTGATCCCAGCACTTTGAGAGGCTGAGGCGGGTGG A G LIMD1 Ensembl:ENSG00000144791 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1447297547 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106099,RMVar_hsa_circ_217433 29103 RMVar_ID_29103 Human_SNP_ID_131570645 A-to-I Human chr3 + 45680889 45680889 45680889 AAAATTAGCTGGGTTTGGTGGCGCACGCCTGTAATCCCAGCTACCTGAGAGGTTGAGGCAGGAGA AAAATTAGCTGGGTTTGGTGGCGCACGCCTGTGATCCCAGCTACCTGAGAGGTTGAGGCAGGAGA A G LIMD1 Ensembl:ENSG00000144791 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,29129909,29129909,29796672,31158229,31158229,31158229,32596459,32596459 RNA-Seq:(High) rs1426540265 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106099,RMVar_hsa_circ_217433 29104 RMVar_ID_29104 Human_SNP_ID_131570647 A-to-I Human chr3 + 45680895 45680895 45680895 AGCTGGGTTTGGTGGCGCACGCCTGTAATCCCAGCTACCTGAGAGGTTGAGGCAGGAGAATCGCT AGCTGGGTTTGGTGGCGCACGCCTGTAATCCCGGCTACCTGAGAGGTTGAGGCAGGAGAATCGCT A G LIMD1 Ensembl:ENSG00000144791 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,29129909,31158229,32596459 RNA-Seq:(High) rs1487057572 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106099,RMVar_hsa_circ_217433 29105 RMVar_ID_29105 Human_SNP_ID_131570654 A-to-I Human chr3 + 45680916 45680916 45680916 CCTGTAATCCCAGCTACCTGAGAGGTTGAGGCAGGAGAATCGCTTGAACCTGGGAGGCAGAGGTT CCTGTAATCCCAGCTACCTGAGAGGTTGAGGCGGGAGAATCGCTTGAACCTGGGAGGCAGAGGTT A G LIMD1 Ensembl:ENSG00000144791 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,29129909,29796672,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs1254048879 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106099,RMVar_hsa_circ_217433 29106 RMVar_ID_29106 Human_SNP_ID_131570661 A-to-I Human chr3 + 45680930 45680930 45680930 TACCTGAGAGGTTGAGGCAGGAGAATCGCTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCCGAGA TACCTGAGAGGTTGAGGCAGGAGAATCGCTTGGACCTGGGAGGCAGAGGTTGCAGTGAGCCGAGA A G LIMD1 Ensembl:ENSG00000144791 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,31158229,31158229,31158229,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs1216707160 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106099,RMVar_hsa_circ_217433 29107 RMVar_ID_29107 Human_SNP_ID_131570665 A-to-I Human chr3 + 45680938 45680937 45680938 AGGTTGAGGCAGGAGAATCGCTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCCGAGATGGTGCCA AGGTTGAGGCAGGAGAATCGCTTGAACCTGGG_GGCAGAGGTTGCAGTGAGCCGAGATGGTGCCA GA G LIMD1 Ensembl:ENSG00000144791 Protein coding 3'UTR GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29796672,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs1397969557 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_106099,RMVar_hsa_circ_217433 29108 RMVar_ID_29108 Human_SNP_ID_131570666 A-to-I Human chr3 + 45680938 45680938 45680938 AGGTTGAGGCAGGAGAATCGCTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCCGAGATGGTGCCA AGGTTGAGGCAGGAGAATCGCTTGAACCTGGGGGGCAGAGGTTGCAGTGAGCCGAGATGGTGCCA A G LIMD1 Ensembl:ENSG00000144791 Protein coding 3'UTR GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29796672,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs944039583 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106099,RMVar_hsa_circ_217433 29109 RMVar_ID_29109 Human_SNP_ID_131570677 A-to-I Human chr3 + 45680992 45680992 45680992 AGATGGTGCCATTGCACTCCGACCTGGGCAACAGAGCGAAACACTGTCTCAAAAAAAAAAAAAAA AGATGGTGCCATTGCACTCCGACCTGGGCAACGGAGCGAAACACTGTCTCAAAAAAAAAAAAAAA A G LIMD1 Ensembl:ENSG00000144791 Protein coding 3'UTR GSE38233;GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,32596459,32596459 RNA-Seq:(High) rs540468319 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106099,RMVar_hsa_circ_217433 29110 RMVar_ID_29110 Human_SNP_ID_131570681 A-to-I Human chr3 + 45680998 45680998 45680998 TGCCATTGCACTCCGACCTGGGCAACAGAGCGAAACACTGTCTCAAAAAAAAAAAAAAAAGTAAC TGCCATTGCACTCCGACCTGGGCAACAGAGCGGAACACTGTCTCAAAAAAAAAAAAAAAAGTAAC A G LIMD1 Ensembl:ENSG00000144791 Protein coding 3'UTR GSE38233;GSE100210;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,29129909,31158229,32596459,32596459 RNA-Seq:(High) rs1319851557 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106099,RMVar_hsa_circ_217433 29111 RMVar_ID_29111 Human_SNP_ID_131583974 A-to-I Human chr3 + 45734586 45734586 45734586 TCAAGTGATCCTCCCACTTTAGCCTTCTGACTACAGGTAGGCACCACCATGCCTGGCTACGTTTT TCAAGTGATCCTCCCACTTTAGCCTTCTGACTGCAGGTAGGCACCACCATGCCTGGCTACGTTTT A G SACM1L Ensembl:ENSG00000211456 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1258198241 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_234,RMVar_hsa_circ_322070,RMVar_hsa_circ_101830,RMVar_hsa_circ_217440,RMVar_hsa_circ_22789,RMVar_hsa_circ_95684,RMVar_hsa_circ_217442,RMVar_hsa_circ_273473,RMVar_hsa_circ_11097,RMVar_hsa_circ_217443 29112 RMVar_ID_29112 Human_SNP_ID_131605716 A-to-I Human chr3 - 45825909 45825909 45825909 CCCATGGGTAAAAATAAATAATAGCATTGTTAAAGATAGTTATTACCAAAAAAAGAGAGTTATTA CCCATGGGTAAAAATAAATAATAGCATTGTTAGAGATAGTTATTACCAAAAAAAGAGAGTTATTA T C LZTFL1 Ensembl:ENSG00000163818 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs560217970 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_602745,Human_RBP_ID_27718991 29113 RMVar_ID_29113 Human_SNP_ID_131627513 A-to-I Human chr3 - 45924998 45924998 45924998 TTGAATCCAGGAGGCACAGGTTGCAGTGAGCCAAGATCACGACACTGCACTCTAGCCTGGGCAAC TTGAATCCAGGAGGCACAGGTTGCAGTGAGCCGAGATCACGACACTGCACTCTAGCCTGGGCAAC T C FYCO1 Ensembl:ENSG00000163820 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1349877325 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266342,RMVar_hsa_circ_98045,RMVar_hsa_circ_81562,RMVar_hsa_circ_217454,RMVar_hsa_circ_217455 29114 RMVar_ID_29114 Human_SNP_ID_131872045 A-to-I Human chr3 - 46950380 46950380 46950380 TTGAGCCTAGGAATTTCAGGCTGTGGTAAGCTATGATTGCACCATGCATTCCAGCCTGGACAGCT TTGAGCCTAGGAATTTCAGGCTGTGGTAAGCTGTGATTGCACCATGCATTCCAGCCTGGACAGCT T C CCDC12 Ensembl:ENSG00000160799 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs925586922 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111160,RMVar_hsa_circ_217471 29115 RMVar_ID_29115 Human_SNP_ID_131903102 A-to-I Human chr3 - 47065643 47065643 47065643 GTGTGCCACCATGCCTGGTTATTTATTTATTTATTTATTTTTTGTAGAGACAGAGTCTCGCTATG GTGTGCCACCATGCCTGGTTATTTATTTATTTTTTTATTTTTTGTAGAGACAGAGTCTCGCTATG T A SETD2 Ensembl:ENSG00000181555 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs999907610 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14839048 RMVar_hsa_circ_217494,RMVar_hsa_circ_347879,RMVar_hsa_circ_366713,RMVar_hsa_circ_372225,RMVar_hsa_circ_363742,RMVar_hsa_circ_346628,RMVar_hsa_circ_87179,RMVar_hsa_circ_273997,RMVar_hsa_circ_269241,RMVar_hsa_circ_75052,RMVar_hsa_circ_217495,RMVar_hsa_circ_93481,RMVar_hsa_circ_30753,RMVar_hsa_circ_297192,RMVar_hsa_circ_217492,RMVar_hsa_circ_217493,RMVar_hsa_circ_217491,RMVar_hsa_circ_302200,RMVar_hsa_circ_217501,RMVar_hsa_circ_292757,RMVar_hsa_circ_117573,RMVar_hsa_circ_346957,RMVar_hsa_circ_377686,RMVar_hsa_circ_217502,RMVar_hsa_circ_374825,RMVar_hsa_circ_341417,RMVar_hsa_circ_283853,RMVar_hsa_circ_283442,RMVar_hsa_circ_108279,RMVar_hsa_circ_109023,RMVar_hsa_circ_99479,RMVar_hsa_circ_217505,RMVar_hsa_circ_217509,RMVar_hsa_circ_217511,RMVar_hsa_circ_217512,RMVar_hsa_circ_217510,RMVar_hsa_circ_217507,RMVar_hsa_circ_217508,RMVar_hsa_circ_217506,RMVar_hsa_circ_217503,RMVar_hsa_circ_217504,RMVar_hsa_circ_268475,RMVar_hsa_circ_312623,RMVar_hsa_circ_365047,RMVar_hsa_circ_311491,RMVar_hsa_circ_42133,RMVar_hsa_circ_217516,RMVar_hsa_circ_217515,RMVar_hsa_circ_366857 29116 RMVar_ID_29116 Human_SNP_ID_131903111 A-to-I Human chr3 - 47065691 47065691 47065691 TCAGGCAATCCTCTTGCCTCAGCCTCTTGAGTAGCTGAGACTATAGGTGTGTGCCACCATGCCTG TCAGGCAATCCTCTTGCCTCAGCCTCTTGAGTGGCTGAGACTATAGGTGTGTGCCACCATGCCTG T C SETD2 Ensembl:ENSG00000181555 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1477895765 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_217494,RMVar_hsa_circ_347879,RMVar_hsa_circ_366713,RMVar_hsa_circ_372225,RMVar_hsa_circ_363742,RMVar_hsa_circ_346628,RMVar_hsa_circ_87179,RMVar_hsa_circ_273997,RMVar_hsa_circ_269241,RMVar_hsa_circ_75052,RMVar_hsa_circ_217495,RMVar_hsa_circ_93481,RMVar_hsa_circ_30753,RMVar_hsa_circ_297192,RMVar_hsa_circ_217492,RMVar_hsa_circ_217493,RMVar_hsa_circ_217491,RMVar_hsa_circ_302200,RMVar_hsa_circ_217501,RMVar_hsa_circ_292757,RMVar_hsa_circ_117573,RMVar_hsa_circ_346957,RMVar_hsa_circ_377686,RMVar_hsa_circ_217502,RMVar_hsa_circ_374825,RMVar_hsa_circ_341417,RMVar_hsa_circ_283853,RMVar_hsa_circ_283442,RMVar_hsa_circ_108279,RMVar_hsa_circ_109023,RMVar_hsa_circ_99479,RMVar_hsa_circ_217505,RMVar_hsa_circ_217509,RMVar_hsa_circ_217511,RMVar_hsa_circ_217512,RMVar_hsa_circ_217510,RMVar_hsa_circ_217507,RMVar_hsa_circ_217508,RMVar_hsa_circ_217506,RMVar_hsa_circ_217503,RMVar_hsa_circ_217504,RMVar_hsa_circ_268475,RMVar_hsa_circ_312623,RMVar_hsa_circ_365047,RMVar_hsa_circ_311491,RMVar_hsa_circ_42133,RMVar_hsa_circ_217516,RMVar_hsa_circ_217515,RMVar_hsa_circ_366857 29117 RMVar_ID_29117 Human_SNP_ID_131903115 A-to-I Human chr3 - 47065717 47065717 47065717 CTCACTGCAGCCTTGAACTCCTGGGCTCAGGCAATCCTCTTGCCTCAGCCTCTTGAGTAGCTGAG CTCACTGCAGCCTTGAACTCCTGGGCTCAGGCCATCCTCTTGCCTCAGCCTCTTGAGTAGCTGAG T G SETD2 Ensembl:ENSG00000181555 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs755683177 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_217494,RMVar_hsa_circ_347879,RMVar_hsa_circ_366713,RMVar_hsa_circ_372225,RMVar_hsa_circ_363742,RMVar_hsa_circ_346628,RMVar_hsa_circ_87179,RMVar_hsa_circ_273997,RMVar_hsa_circ_269241,RMVar_hsa_circ_75052,RMVar_hsa_circ_217495,RMVar_hsa_circ_93481,RMVar_hsa_circ_30753,RMVar_hsa_circ_297192,RMVar_hsa_circ_217492,RMVar_hsa_circ_217493,RMVar_hsa_circ_217491,RMVar_hsa_circ_302200,RMVar_hsa_circ_217501,RMVar_hsa_circ_292757,RMVar_hsa_circ_117573,RMVar_hsa_circ_346957,RMVar_hsa_circ_377686,RMVar_hsa_circ_217502,RMVar_hsa_circ_374825,RMVar_hsa_circ_341417,RMVar_hsa_circ_283853,RMVar_hsa_circ_283442,RMVar_hsa_circ_108279,RMVar_hsa_circ_109023,RMVar_hsa_circ_99479,RMVar_hsa_circ_217505,RMVar_hsa_circ_217509,RMVar_hsa_circ_217511,RMVar_hsa_circ_217512,RMVar_hsa_circ_217510,RMVar_hsa_circ_217507,RMVar_hsa_circ_217508,RMVar_hsa_circ_217506,RMVar_hsa_circ_217503,RMVar_hsa_circ_217504,RMVar_hsa_circ_268475,RMVar_hsa_circ_312623,RMVar_hsa_circ_365047,RMVar_hsa_circ_311491,RMVar_hsa_circ_42133,RMVar_hsa_circ_217516,RMVar_hsa_circ_217515,RMVar_hsa_circ_366857 29118 RMVar_ID_29118 Human_SNP_ID_131903117 A-to-I Human chr3 - 47065721 47065721 47065721 AGCTCTCACTGCAGCCTTGAACTCCTGGGCTCAGGCAATCCTCTTGCCTCAGCCTCTTGAGTAGC AGCTCTCACTGCAGCCTTGAACTCCTGGGCTCGGGCAATCCTCTTGCCTCAGCCTCTTGAGTAGC T C SETD2 Ensembl:ENSG00000181555 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs912394384 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_217494,RMVar_hsa_circ_347879,RMVar_hsa_circ_366713,RMVar_hsa_circ_372225,RMVar_hsa_circ_363742,RMVar_hsa_circ_346628,RMVar_hsa_circ_87179,RMVar_hsa_circ_273997,RMVar_hsa_circ_269241,RMVar_hsa_circ_75052,RMVar_hsa_circ_217495,RMVar_hsa_circ_93481,RMVar_hsa_circ_30753,RMVar_hsa_circ_297192,RMVar_hsa_circ_217492,RMVar_hsa_circ_217493,RMVar_hsa_circ_217491,RMVar_hsa_circ_302200,RMVar_hsa_circ_217501,RMVar_hsa_circ_292757,RMVar_hsa_circ_117573,RMVar_hsa_circ_346957,RMVar_hsa_circ_377686,RMVar_hsa_circ_217502,RMVar_hsa_circ_374825,RMVar_hsa_circ_341417,RMVar_hsa_circ_283853,RMVar_hsa_circ_283442,RMVar_hsa_circ_108279,RMVar_hsa_circ_109023,RMVar_hsa_circ_99479,RMVar_hsa_circ_217505,RMVar_hsa_circ_217509,RMVar_hsa_circ_217511,RMVar_hsa_circ_217512,RMVar_hsa_circ_217510,RMVar_hsa_circ_217507,RMVar_hsa_circ_217508,RMVar_hsa_circ_217506,RMVar_hsa_circ_217503,RMVar_hsa_circ_217504,RMVar_hsa_circ_268475,RMVar_hsa_circ_312623,RMVar_hsa_circ_365047,RMVar_hsa_circ_311491,RMVar_hsa_circ_42133,RMVar_hsa_circ_217516,RMVar_hsa_circ_217515,RMVar_hsa_circ_366857 29119 RMVar_ID_29119 Human_SNP_ID_131903303 A-to-I Human chr3 - 47066575 47066575 47066575 GGAAGTTGAAGCAGGTGGATTGCTTGAGCCCAAGAGTTTGAGACCAGCCTGGGAAACATGGTGAA GGAAGTTGAAGCAGGTGGATTGCTTGAGCCCAGGAGTTTGAGACCAGCCTGGGAAACATGGTGAA T C SETD2 Ensembl:ENSG00000181555 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1428923833 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_217494,RMVar_hsa_circ_347879,RMVar_hsa_circ_366713,RMVar_hsa_circ_372225,RMVar_hsa_circ_363742,RMVar_hsa_circ_346628,RMVar_hsa_circ_87179,RMVar_hsa_circ_273997,RMVar_hsa_circ_269241,RMVar_hsa_circ_75052,RMVar_hsa_circ_217495,RMVar_hsa_circ_93481,RMVar_hsa_circ_30753,RMVar_hsa_circ_297192,RMVar_hsa_circ_217492,RMVar_hsa_circ_217493,RMVar_hsa_circ_217491,RMVar_hsa_circ_302200,RMVar_hsa_circ_217501,RMVar_hsa_circ_292757,RMVar_hsa_circ_117573,RMVar_hsa_circ_346957,RMVar_hsa_circ_377686,RMVar_hsa_circ_217502,RMVar_hsa_circ_374825,RMVar_hsa_circ_341417,RMVar_hsa_circ_283853,RMVar_hsa_circ_283442,RMVar_hsa_circ_108279,RMVar_hsa_circ_109023,RMVar_hsa_circ_99479,RMVar_hsa_circ_217505,RMVar_hsa_circ_217509,RMVar_hsa_circ_217511,RMVar_hsa_circ_217512,RMVar_hsa_circ_217510,RMVar_hsa_circ_217507,RMVar_hsa_circ_217508,RMVar_hsa_circ_217506,RMVar_hsa_circ_217503,RMVar_hsa_circ_217504,RMVar_hsa_circ_268475,RMVar_hsa_circ_312623,RMVar_hsa_circ_365047,RMVar_hsa_circ_311491,RMVar_hsa_circ_42133,RMVar_hsa_circ_217516,RMVar_hsa_circ_217515,RMVar_hsa_circ_366857 29120 RMVar_ID_29120 Human_SNP_ID_131904663 A-to-I Human chr3 - 47072186 47072186 47072186 CTCCTGCCTCAGCCTCCCCAGTAGCTGGGACTACAGGCACCCGCCACCAGGCCTGGCTAATTTTT CTCCTGCCTCAGCCTCCCCAGTAGCTGGGACTGCAGGCACCCGCCACCAGGCCTGGCTAATTTTT T C SETD2 Ensembl:ENSG00000181555 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1051034749 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_217494,RMVar_hsa_circ_347879,RMVar_hsa_circ_366713,RMVar_hsa_circ_372225,RMVar_hsa_circ_363742,RMVar_hsa_circ_346628,RMVar_hsa_circ_87179,RMVar_hsa_circ_269241,RMVar_hsa_circ_75052,RMVar_hsa_circ_93481,RMVar_hsa_circ_30753,RMVar_hsa_circ_217492,RMVar_hsa_circ_217493,RMVar_hsa_circ_217491,RMVar_hsa_circ_302200,RMVar_hsa_circ_217501,RMVar_hsa_circ_117573,RMVar_hsa_circ_346957,RMVar_hsa_circ_377686,RMVar_hsa_circ_374825,RMVar_hsa_circ_341417,RMVar_hsa_circ_283853,RMVar_hsa_circ_108279,RMVar_hsa_circ_109023,RMVar_hsa_circ_99479,RMVar_hsa_circ_217505,RMVar_hsa_circ_217509,RMVar_hsa_circ_217511,RMVar_hsa_circ_217510,RMVar_hsa_circ_217507,RMVar_hsa_circ_217508,RMVar_hsa_circ_217506,RMVar_hsa_circ_217503,RMVar_hsa_circ_217504,RMVar_hsa_circ_268475,RMVar_hsa_circ_365047,RMVar_hsa_circ_311491,RMVar_hsa_circ_42133,RMVar_hsa_circ_57748,RMVar_hsa_circ_319943,RMVar_hsa_circ_332546,RMVar_hsa_circ_217515,RMVar_hsa_circ_329107,RMVar_hsa_circ_66161,RMVar_hsa_circ_274658,RMVar_hsa_circ_62887,RMVar_hsa_circ_217518,RMVar_hsa_circ_55312,RMVar_hsa_circ_217519,RMVar_hsa_circ_217517 29121 RMVar_ID_29121 Human_SNP_ID_131904667 A-to-I Human chr3 - 47072196 47072196 47072196 TCATGCCATTCTCCTGCCTCAGCCTCCCCAGTAGCTGGGACTACAGGCACCCGCCACCAGGCCTG TCATGCCATTCTCCTGCCTCAGCCTCCCCAGTCGCTGGGACTACAGGCACCCGCCACCAGGCCTG T G SETD2 Ensembl:ENSG00000181555 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs891151061 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_217494,RMVar_hsa_circ_347879,RMVar_hsa_circ_366713,RMVar_hsa_circ_372225,RMVar_hsa_circ_363742,RMVar_hsa_circ_346628,RMVar_hsa_circ_87179,RMVar_hsa_circ_269241,RMVar_hsa_circ_75052,RMVar_hsa_circ_93481,RMVar_hsa_circ_30753,RMVar_hsa_circ_217492,RMVar_hsa_circ_217493,RMVar_hsa_circ_217491,RMVar_hsa_circ_302200,RMVar_hsa_circ_217501,RMVar_hsa_circ_117573,RMVar_hsa_circ_346957,RMVar_hsa_circ_377686,RMVar_hsa_circ_374825,RMVar_hsa_circ_341417,RMVar_hsa_circ_283853,RMVar_hsa_circ_108279,RMVar_hsa_circ_109023,RMVar_hsa_circ_99479,RMVar_hsa_circ_217505,RMVar_hsa_circ_217509,RMVar_hsa_circ_217511,RMVar_hsa_circ_217510,RMVar_hsa_circ_217507,RMVar_hsa_circ_217508,RMVar_hsa_circ_217506,RMVar_hsa_circ_217503,RMVar_hsa_circ_217504,RMVar_hsa_circ_268475,RMVar_hsa_circ_365047,RMVar_hsa_circ_311491,RMVar_hsa_circ_42133,RMVar_hsa_circ_57748,RMVar_hsa_circ_319943,RMVar_hsa_circ_332546,RMVar_hsa_circ_217515,RMVar_hsa_circ_329107,RMVar_hsa_circ_66161,RMVar_hsa_circ_274658,RMVar_hsa_circ_62887,RMVar_hsa_circ_217518,RMVar_hsa_circ_55312,RMVar_hsa_circ_217519,RMVar_hsa_circ_217517 29122 RMVar_ID_29122 Human_SNP_ID_131911129 A-to-I Human chr3 - 47100107 47100107 47100107 GAAACCCCGTCTCTACTAAGAATACAAAAAATAGCCAGGTGGGGTGGCACATGCCTGTAATCCTA GAAACCCCGTCTCTACTAAGAATACAAAAAATCGCCAGGTGGGGTGGCACATGCCTGTAATCCTA T G SETD2 Ensembl:ENSG00000181555 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs553130454 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_366713,RMVar_hsa_circ_372225,RMVar_hsa_circ_363742,RMVar_hsa_circ_87179,RMVar_hsa_circ_24475,RMVar_hsa_circ_93481,RMVar_hsa_circ_217492,RMVar_hsa_circ_217491,RMVar_hsa_circ_117573,RMVar_hsa_circ_283853,RMVar_hsa_circ_108279,RMVar_hsa_circ_109023,RMVar_hsa_circ_99479,RMVar_hsa_circ_217505,RMVar_hsa_circ_217507,RMVar_hsa_circ_217506,RMVar_hsa_circ_217503,RMVar_hsa_circ_217504,RMVar_hsa_circ_268475,RMVar_hsa_circ_365047,RMVar_hsa_circ_57748,RMVar_hsa_circ_332546,RMVar_hsa_circ_62887,RMVar_hsa_circ_55312,RMVar_hsa_circ_280976,RMVar_hsa_circ_320942,RMVar_hsa_circ_361101,RMVar_hsa_circ_86365,RMVar_hsa_circ_127672,RMVar_hsa_circ_50911,RMVar_hsa_circ_217522,RMVar_hsa_circ_217524,RMVar_hsa_circ_217523,RMVar_hsa_circ_284202,RMVar_hsa_circ_309009,RMVar_hsa_circ_305791,RMVar_hsa_circ_120152,RMVar_hsa_circ_217532,RMVar_hsa_circ_217530,RMVar_hsa_circ_217531,RMVar_hsa_circ_217529,RMVar_hsa_circ_300537,RMVar_hsa_circ_298401,RMVar_hsa_circ_286958,RMVar_hsa_circ_307355,RMVar_hsa_circ_378001,RMVar_hsa_circ_351229,RMVar_hsa_circ_290667,RMVar_hsa_circ_282250,RMVar_hsa_circ_217534,RMVar_hsa_circ_217536,RMVar_hsa_circ_217537,RMVar_hsa_circ_217538,RMVar_hsa_circ_217535,RMVar_hsa_circ_217533 29123 RMVar_ID_29123 Human_SNP_ID_131914623 A-to-I Human chr3 - 47113756 47113756 47113756 TGGCTCACTGGAACCTCTACCTCCCGGATTCAAGCAATTCTCCTGCCTTAGCCTCTCAAGTAGCT TGGCTCACTGGAACCTCTACCTCCCGGATTCAGGCAATTCTCCTGCCTTAGCCTCTCAAGTAGCT T C SETD2 Ensembl:ENSG00000181555 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs931619556 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24428433 RMVar_hsa_circ_363742,RMVar_hsa_circ_24475,RMVar_hsa_circ_117573,RMVar_hsa_circ_108279,RMVar_hsa_circ_109023,RMVar_hsa_circ_99479,RMVar_hsa_circ_217505,RMVar_hsa_circ_217506,RMVar_hsa_circ_217503,RMVar_hsa_circ_217504,RMVar_hsa_circ_57748,RMVar_hsa_circ_86365,RMVar_hsa_circ_127672,RMVar_hsa_circ_50911,RMVar_hsa_circ_217522,RMVar_hsa_circ_120152,RMVar_hsa_circ_217532,RMVar_hsa_circ_217531,RMVar_hsa_circ_300537,RMVar_hsa_circ_286958,RMVar_hsa_circ_378001,RMVar_hsa_circ_351229,RMVar_hsa_circ_217534,RMVar_hsa_circ_217535,RMVar_hsa_circ_57010,RMVar_hsa_circ_217533,RMVar_hsa_circ_352364,RMVar_hsa_circ_217541,RMVar_hsa_circ_313463,RMVar_hsa_circ_217543,RMVar_hsa_circ_291066,RMVar_hsa_circ_337046,RMVar_hsa_circ_373460,RMVar_hsa_circ_119859,RMVar_hsa_circ_217545,RMVar_hsa_circ_217547,RMVar_hsa_circ_217548,RMVar_hsa_circ_217546,RMVar_hsa_circ_217544 29124 RMVar_ID_29124 Human_SNP_ID_131914632 A-to-I Human chr3 - 47113795 47113795 47113795 TCACTCTTTCACCCAGACTGGAGTGCAGTGGCACGATCTTGGCTCACTGGAACCTCTACCTCCCG TCACTCTTTCACCCAGACTGGAGTGCAGTGGCGCGATCTTGGCTCACTGGAACCTCTACCTCCCG T C SETD2 Ensembl:ENSG00000181555 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1244607390 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24428433 RMVar_hsa_circ_363742,RMVar_hsa_circ_24475,RMVar_hsa_circ_117573,RMVar_hsa_circ_108279,RMVar_hsa_circ_109023,RMVar_hsa_circ_99479,RMVar_hsa_circ_217505,RMVar_hsa_circ_217506,RMVar_hsa_circ_217503,RMVar_hsa_circ_217504,RMVar_hsa_circ_57748,RMVar_hsa_circ_86365,RMVar_hsa_circ_127672,RMVar_hsa_circ_50911,RMVar_hsa_circ_217522,RMVar_hsa_circ_120152,RMVar_hsa_circ_217532,RMVar_hsa_circ_217531,RMVar_hsa_circ_300537,RMVar_hsa_circ_286958,RMVar_hsa_circ_378001,RMVar_hsa_circ_351229,RMVar_hsa_circ_217534,RMVar_hsa_circ_217535,RMVar_hsa_circ_57010,RMVar_hsa_circ_217533,RMVar_hsa_circ_352364,RMVar_hsa_circ_217541,RMVar_hsa_circ_313463,RMVar_hsa_circ_217543,RMVar_hsa_circ_291066,RMVar_hsa_circ_337046,RMVar_hsa_circ_373460,RMVar_hsa_circ_119859,RMVar_hsa_circ_217545,RMVar_hsa_circ_217547,RMVar_hsa_circ_217548,RMVar_hsa_circ_217546,RMVar_hsa_circ_217544 29125 RMVar_ID_29125 Human_SNP_ID_131919801 A-to-I Human chr3 - 47133326 47133326 47133326 ATTTCCACTGGGTACAGTTGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTAAGGCGGGAGGA ATTTCCACTGGGTACAGTTGCTCATGCCTGTAGTCCCAGCACTTTGGGAGGCTAAGGCGGGAGGA T C SETD2 Ensembl:ENSG00000181555 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1361219823 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17573405 RMVar_hsa_circ_117573,RMVar_hsa_circ_217503 29126 RMVar_ID_29126 Human_SNP_ID_131920129 A-to-I Human chr3 - 47134764 47134764 47134764 CAAAAATCAGCCATGTGTGGCGGCACATGCCTATAATCCCAGCTACTCCAGTGGCTGAGGGAGGA CAAAAATCAGCCATGTGTGGCGGCACATGCCTGTAATCCCAGCTACTCCAGTGGCTGAGGGAGGA T C SETD2 Ensembl:ENSG00000181555 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs966383604 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117573,RMVar_hsa_circ_217503 29127 RMVar_ID_29127 Human_SNP_ID_131921509 A-to-I Human chr3 - 47140698 47140698 47140698 TGCCACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGATTTCACCATGTTGGCCAGGC TGCCACCATGCCTGGCTAATTTTTGTATTTTTGGTAGAGACAGGATTTCACCATGTTGGCCAGGC T C SETD2 Ensembl:ENSG00000181555 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1001476185 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117573,RMVar_hsa_circ_217503 29128 RMVar_ID_29128 Human_SNP_ID_131921525 A-to-I Human chr3 - 47140761 47140761 47140761 CCCCACTGGGATTCAAGTAATTCTTGTGCCTTAGCCTCCCGAGTAGCTGGGATTACAGATGACTG CCCCACTGGGATTCAAGTAATTCTTGTGCCTTGGCCTCCCGAGTAGCTGGGATTACAGATGACTG T C SETD2 Ensembl:ENSG00000181555 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1454373470 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117573,RMVar_hsa_circ_217503 29129 RMVar_ID_29129 Human_SNP_ID_131921526 A-to-I Human chr3 - 47140778 47140778 47140778 GCTCACTGCAACCTCCACCCCACTGGGATTCAAGTAATTCTTGTGCCTTAGCCTCCCGAGTAGCT GCTCACTGCAACCTCCACCCCACTGGGATTCAGGTAATTCTTGTGCCTTAGCCTCCCGAGTAGCT T C SETD2 Ensembl:ENSG00000181555 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs535282309 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117573,RMVar_hsa_circ_217503 29130 RMVar_ID_29130 Human_SNP_ID_131921536 A-to-I Human chr3 - 47140811 47140811 47140811 TCACCCAGGCTGGAGTGCAATGGCGCAATCTCAGCTCACTGCAACCTCCACCCCACTGGGATTCA TCACCCAGGCTGGAGTGCAATGGCGCAATCTCGGCTCACTGCAACCTCCACCCCACTGGGATTCA T C SETD2 Ensembl:ENSG00000181555 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1028872374 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7200326,Human_RBP_ID_14840904 RMVar_hsa_circ_117573,RMVar_hsa_circ_217503 29131 RMVar_ID_29131 Human_SNP_ID_131921891 A-to-I Human chr3 - 47142328 47142328 47142328 ATTTTGCTTATTTTTTGTAGAGGCGAGGTCTCACTATGTTGCTCAGGATGGTCTCGAACTCCTAG ATTTTGCTTATTTTTTGTAGAGGCGAGGTCTCGCTATGTTGCTCAGGATGGTCTCGAACTCCTAG T C SETD2 Ensembl:ENSG00000181555 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1048840147 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14840961 RMVar_hsa_circ_117573,RMVar_hsa_circ_217503 29132 RMVar_ID_29132 Human_SNP_ID_131921905 A-to-I Human chr3 - 47142387 47142387 47142387 TTCTCACCTCAGCCTCCTGAGTAGCTGGGACTACAGGCGCACACCATCACACCTGGCTAATTTTG TTCTCACCTCAGCCTCCTGAGTAGCTGGGACTGCAGGCGCACACCATCACACCTGGCTAATTTTG T C SETD2 Ensembl:ENSG00000181555 Protein coding intron GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs1244477823 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117573,RMVar_hsa_circ_217503 29133 RMVar_ID_29133 Human_SNP_ID_131922092 A-to-I Human chr3 - 47143048 47143048 47143048 GGCTCAAGTGATCCTCCAGCATCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGACCCACCATGC GGCTCAAGTGATCCTCCAGCATCAGCCTCCCAGAGTGCTGGGATTACAGGTGTGACCCACCATGC T C SETD2 Ensembl:ENSG00000181555 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1235447825 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17573589 RMVar_hsa_circ_117573,RMVar_hsa_circ_217503 29134 RMVar_ID_29134 Human_SNP_ID_131922098 A-to-I Human chr3 - 47143074 47143074 47143074 TGCCCAGACTAGTCTTGAGCTCCTTGGGCTCAAGTGATCCTCCAGCATCAGCCTCCCAAAGTGCT TGCCCAGACTAGTCTTGAGCTCCTTGGGCTCAGGTGATCCTCCAGCATCAGCCTCCCAAAGTGCT T C SETD2 Ensembl:ENSG00000181555 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs773179666 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17573589 RMVar_hsa_circ_117573,RMVar_hsa_circ_217503 29135 RMVar_ID_29135 Human_SNP_ID_131922099 A-to-I Human chr3 - 47143074 47143074 47143074 TGCCCAGACTAGTCTTGAGCTCCTTGGGCTCAAGTGATCCTCCAGCATCAGCCTCCCAAAGTGCT TGCCCAGACTAGTCTTGAGCTCCTTGGGCTCACGTGATCCTCCAGCATCAGCCTCCCAAAGTGCT T G SETD2 Ensembl:ENSG00000181555 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs773179666 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17573589 RMVar_hsa_circ_117573,RMVar_hsa_circ_217503 29136 RMVar_ID_29136 Human_SNP_ID_131922524 A-to-I Human chr3 - 47144868 47144868 47144868 CAGCTCACTGCAGCCTCAGCTTCCCGGGTTCAAGCGATTCTCGTACCTCAGCCTCCCGAGTAGCT CAGCTCACTGCAGCCTCAGCTTCCCGGGTTCAGGCGATTCTCGTACCTCAGCCTCCCGAGTAGCT T C SETD2 Ensembl:ENSG00000181555 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1214998372 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117573,RMVar_hsa_circ_217503 29137 RMVar_ID_29137 Human_SNP_ID_131922918 A-to-I Human chr3 - 47146546 47146546 47146546 CTCGGCTTACTGCAACCTCTGCCTCTGGATTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGC CTCGGCTTACTGCAACCTCTGCCTCTGGATTCGAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGC T C SETD2 Ensembl:ENSG00000181555 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1233525075 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117573,RMVar_hsa_circ_217503 29138 RMVar_ID_29138 Human_SNP_ID_131922923 A-to-I Human chr3 - 47146583 47146583 47146583 TCACTGTGTCGCCCAGGTTGGAGAGTAGTGGCATGACCTCGGCTTACTGCAACCTCTGCCTCTGG TCACTGTGTCGCCCAGGTTGGAGAGTAGTGGCGTGACCTCGGCTTACTGCAACCTCTGCCTCTGG T C SETD2 Ensembl:ENSG00000181555 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs940799118 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14841127,Human_RBP_ID_22726118 RMVar_hsa_circ_117573,RMVar_hsa_circ_217503 29139 RMVar_ID_29139 Human_SNP_ID_131924691 A-to-I Human chr3 - 47153670 47153670 47153670 CAGTTCACTGTAGCCTCGAACTCTTGGGCTCAAGCAATCCTCCTGCCTCAGCCTCCCAAGTAGCT CAGTTCACTGTAGCCTCGAACTCTTGGGCTCACGCAATCCTCCTGCCTCAGCCTCCCAAGTAGCT T G SETD2 Ensembl:ENSG00000181555 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs570271289 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14841439 RMVar_hsa_circ_117573,RMVar_hsa_circ_217503 29140 RMVar_ID_29140 Human_SNP_ID_131924692 A-to-I Human chr3 - 47153671 47153671 47153671 CCAGTTCACTGTAGCCTCGAACTCTTGGGCTCAAGCAATCCTCCTGCCTCAGCCTCCCAAGTAGC CCAGTTCACTGTAGCCTCGAACTCTTGGGCTCCAGCAATCCTCCTGCCTCAGCCTCCCAAGTAGC T G SETD2 Ensembl:ENSG00000181555 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1438954429 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14841439 RMVar_hsa_circ_117573,RMVar_hsa_circ_217503 29141 RMVar_ID_29141 Human_SNP_ID_131929192 A-to-I Human chr3 + 47172267 47172267 47172267 GTGCTGATGTATAATTGTTTTTTAGTTTTTTTAGAAACAGGGTCTCGCTATGTTGCCCAGGTTGG GTGCTGATGTATAATTGTTTTTTAGTTTTTTTGGAAACAGGGTCTCGCTATGTTGCCCAGGTTGG A G KIF9-AS1 Ensembl:ENSG00000227398 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1451284262 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_217557,RMVar_hsa_circ_82426,RMVar_hsa_circ_217555 29142 RMVar_ID_29142 Human_SNP_ID_131929344 A-to-I Human chr3 + 47173033 47173033 47173033 ACTGTAATCCCAGAACTTTGGGAGGCTGATGTAGGAGGATCACTTGAGCTCAGGAGTTGGACACC ACTGTAATCCCAGAACTTTGGGAGGCTGATGTTGGAGGATCACTTGAGCTCAGGAGTTGGACACC A T KIF9-AS1 Ensembl:ENSG00000227398 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1425441657 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_217557,RMVar_hsa_circ_82426,RMVar_hsa_circ_217555 29143 RMVar_ID_29143 Human_SNP_ID_131929436 A-to-I Human chr3 + 47173481 47173481 47173481 ACAAAAATTAACCGGGCATGGCACGCGCTGGTAATCCCAGCTAGTCGGGAGGCTGAGGAAGAAGA ACAAAAATTAACCGGGCATGGCACGCGCTGGTTATCCCAGCTAGTCGGGAGGCTGAGGAAGAAGA A T KIF9-AS1 Ensembl:ENSG00000227398 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054681202 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_217557,RMVar_hsa_circ_82426,RMVar_hsa_circ_217555 29144 RMVar_ID_29144 Human_SNP_ID_131930488 A-to-I Human chr3 + 47178377 47178377 47178377 GAAAGAATGATAGATAAAACTAAATGGAGGCCAGGTGCAGTGGCTCACACCTGTAATCCCAGCAC GAAAGAATGATAGATAAAACTAAATGGAGGCCGGGTGCAGTGGCTCACACCTGTAATCCCAGCAC A G KIF9-AS1 Ensembl:ENSG00000227398 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1194310174 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82426,RMVar_hsa_circ_217555 29145 RMVar_ID_29145 Human_SNP_ID_131931108 A-to-I Human chr3 + 47181166 47181166 47181166 CAAGACCAGCCTGGGCAATATGGCAAAACTCTATCTCTACAAAAAAACACAAAAAAATTAGCCAG CAAGACCAGCCTGGGCAATATGGCAAAACTCTCTCTCTACAAAAAAACACAAAAAAATTAGCCAG A C KIF9-AS1 Ensembl:ENSG00000227398 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1395834187 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5250247 RMVar_hsa_circ_82426,RMVar_hsa_circ_217555 29146 RMVar_ID_29146 Human_SNP_ID_131931850 A-to-I Human chr3 + 47183999 47183999 47183999 GCACTGTTTCCTGGGCTGCAGTGCAGTGGCACAATCTCGGCTCACTGCAACCTCCACCTCCTGTG GCACTGTTTCCTGGGCTGCAGTGCAGTGGCACCATCTCGGCTCACTGCAACCTCCACCTCCTGTG A C KIF9-AS1 Ensembl:ENSG00000227398 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs912807612 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14979241 RMVar_hsa_circ_82426,RMVar_hsa_circ_217555 29147 RMVar_ID_29147 Human_SNP_ID_131932515 A-to-I Human chr3 + 47186755 47186755 47186755 GTGGTGGCTCATGCCTGTAATCCCAGCACTTTAGGAGGCCAAGGCAGGTGGACAACTTGAGGCCA GTGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGTGGACAACTTGAGGCCA A G KIF9-AS1 Ensembl:ENSG00000227398 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs374291008 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82426,RMVar_hsa_circ_217555 29148 RMVar_ID_29148 Human_SNP_ID_131932517 A-to-I Human chr3 + 47186768 47186768 47186768 CCTGTAATCCCAGCACTTTAGGAGGCCAAGGCAGGTGGACAACTTGAGGCCAGGAGTTGGAGACC CCTGTAATCCCAGCACTTTAGGAGGCCAAGGCGGGTGGACAACTTGAGGCCAGGAGTTGGAGACC A G KIF9-AS1 Ensembl:ENSG00000227398 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1343560235 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82426,RMVar_hsa_circ_217555 29149 RMVar_ID_29149 Human_SNP_ID_131932777 A-to-I Human chr3 + 47187963 47187963 47187963 CTCACTGCATCCTCCGCCTCCTGGGTTCAAGCAATTCTCCTGCCTCAACCTCCTGAGTAGCTGAG CTCACTGCATCCTCCGCCTCCTGGGTTCAAGCTATTCTCCTGCCTCAACCTCCTGAGTAGCTGAG A T KIF9-AS1 Ensembl:ENSG00000227398 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1405118963 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82426,RMVar_hsa_circ_217555 29150 RMVar_ID_29150 Human_SNP_ID_131932999 A-to-I Human chr3 + 47188903 47188896 47188904 CCGAGGTGGGTAGATCACGAGGTCAGGAGTTCAAGACCGGCCTGGCAAACATGGTGAAACCCCGT CCGAGGTGGGTAGATCACGAGGTCAG________GACCGGCCTGGCAAACATGGTGAAACCCCGT GGAGTTCAA G KIF9-AS1 Ensembl:ENSG00000227398 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1473674457 Functional Loss DEL dbSNP153 27..34 33 - - - RMVar_hsa_circ_82426,RMVar_hsa_circ_217555 29151 RMVar_ID_29151 Human_SNP_ID_131933000 A-to-I Human chr3 + 47188903 47188903 47188903 CCGAGGTGGGTAGATCACGAGGTCAGGAGTTCAAGACCGGCCTGGCAAACATGGTGAAACCCCGT CCGAGGTGGGTAGATCACGAGGTCAGGAGTTCCAGACCGGCCTGGCAAACATGGTGAAACCCCGT A C KIF9-AS1 Ensembl:ENSG00000227398 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs959126198 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82426,RMVar_hsa_circ_217555 29152 RMVar_ID_29152 Human_SNP_ID_131941368 A-to-I Human chr3 + 47224691 47224691 47224691 AGAGACCAGCCTGGCCAATATAGTGAAACCCCATCTCTACTACAAATACAAAAGTTTGCTGGGTG AGAGACCAGCCTGGCCAATATAGTGAAACCCCGTCTCTACTACAAATACAAAAGTTTGCTGGGTG A G KIF9-AS1 Ensembl:ENSG00000227398 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1331413827 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82426,RMVar_hsa_circ_217555 29153 RMVar_ID_29153 Human_SNP_ID_131954920 A-to-I Human chr3 - 47279390 47279390 47279390 TCACTGCAACCTCCACCCTCCAGATTCAAGCAATTCTCCTGTCTCAGCCTCCTGAGTAGCTGAGA TCACTGCAACCTCCACCCTCCAGATTCAAGCACTTCTCCTGTCTCAGCCTCCTGAGTAGCTGAGA T G KIF9 Ensembl:ENSG00000088727 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1427307052 Functional Loss SNV dbSNP153 33..33 33 - - - 29154 RMVar_ID_29154 Human_SNP_ID_131956671 A-to-I Human chr3 + 47285459 47285459 47285459 AGGCTGTAGGCTGGGCACCGTGGCTCACGCCTATTATCCCAGCACTTTGGAAGGCCAAGGCGAGT AGGCTGTAGGCTGGGCACCGTGGCTCACGCCTGTTATCCCAGCACTTTGGAAGGCCAAGGCGAGT A G KLHL18 Ensembl:ENSG00000114648 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1171749507 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14842614,Human_RBP_ID_25738834 29155 RMVar_ID_29155 Human_SNP_ID_131960867 A-to-I Human chr3 + 47303957 47303957 47303957 TCCTATGTTGCTCGGGCTGGTCTCGAACTGCTAGCCTGAAGTGATTCTCCCACCTCAGCCTCCCA TCCTATGTTGCTCGGGCTGGTCTCGAACTGCTGGCCTGAAGTGATTCTCCCACCTCAGCCTCCCA A G KLHL18 Ensembl:ENSG00000114648 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1385801169 Functional Loss SNV dbSNP153 33..33 33 - - - 29156 RMVar_ID_29156 Human_SNP_ID_131982688 A-to-I Human chr3 + 47396835 47396835 47396835 ATGTCCCCAGCTACGCAGGAGTCTGAGGAGGGAAGATCACTTGAGCCCAGGAGGTTGGGACTGCA ATGTCCCCAGCTACGCAGGAGTCTGAGGAGGGTAGATCACTTGAGCCCAGGAGGTTGGGACTGCA A T PTPN23 Ensembl:ENSG00000076201 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1007021203 Functional Loss SNV dbSNP153 33..33 33 - - - 29157 RMVar_ID_29157 Human_SNP_ID_131983080 A-to-I Human chr3 + 47398627 47398627 47398627 TCGCTCTGTCGTCCAGGCAGGAGTGCAGTGGCACAATCACGGCTCACTGCAGCCTCCATCTCCCC TCGCTCTGTCGTCCAGGCAGGAGTGCAGTGGCGCAATCACGGCTCACTGCAGCCTCCATCTCCCC A G PTPN23 Ensembl:ENSG00000076201 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1425250857 Functional Loss SNV dbSNP153 33..33 33 - - - 29158 RMVar_ID_29158 Human_SNP_ID_131983101 A-to-I Human chr3 + 47398737 47398737 47398737 CAAGTGCACACCACCGCATCCAGCCAATTTTTAAATTTTTTGTAGAGATGGGGTTCCCCTGTGTT CAAGTGCACACCACCGCATCCAGCCAATTTTTGAATTTTTTGTAGAGATGGGGTTCCCCTGTGTT A G PTPN23 Ensembl:ENSG00000076201 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991679951 Functional Loss SNV dbSNP153 33..33 33 - - - 29159 RMVar_ID_29159 Human_SNP_ID_131984349 A-to-I Human chr3 + 47403962 47403962 47403962 GATACAGAACTGTAGGTCATGCTGAGTGTGGCAGCTCACACCTTTAATCCCATCACTTTGGGAGG GATACAGAACTGTAGGTCATGCTGAGTGTGGCGGCTCACACCTTTAATCCCATCACTTTGGGAGG A G PTPN23 Ensembl:ENSG00000076201 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1168749410 Functional Loss SNV dbSNP153 33..33 33 - - - 29160 RMVar_ID_29160 Human_SNP_ID_131996122 A-to-I Human chr3 - 47441985 47441985 47441985 AAAGATGAACTTTGGCCAGGTGCAGTGCTCATACCTGTAATTCCAACACTGGGAGGCTGAGGTGA AAAGATGAACTTTGGCCAGGTGCAGTGCTCATCCCTGTAATTCCAACACTGGGAGGCTGAGGTGA T G SCAP Ensembl:ENSG00000114650 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1195417434 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14843916 RMVar_hsa_circ_81144,RMVar_hsa_circ_217580,RMVar_hsa_circ_107903,RMVar_hsa_circ_217583,RMVar_hsa_circ_50998,RMVar_hsa_circ_108313,RMVar_hsa_circ_217591,RMVar_hsa_circ_98328,RMVar_hsa_circ_217597,RMVar_hsa_circ_300276,RMVar_hsa_circ_112004,RMVar_hsa_circ_116798,RMVar_hsa_circ_84764,RMVar_hsa_circ_217598,RMVar_hsa_circ_217599,RMVar_hsa_circ_25940,RMVar_hsa_circ_275451,RMVar_hsa_circ_217607,RMVar_hsa_circ_217608,RMVar_hsa_circ_101506,RMVar_hsa_circ_217614,RMVar_hsa_circ_270489,RMVar_hsa_circ_217616,RMVar_hsa_circ_217617 29161 RMVar_ID_29161 Human_SNP_ID_131997561 A-to-I Human chr3 - 47447602 47447602 47447602 CTCACTGTGGCCTCCGCCTCCCGGGTTTAAGCAATTCTCCTGTCTCCGCCTCCCAAGTAGCTGGT CTCACTGTGGCCTCCGCCTCCCGGGTTTAAGCCATTCTCCTGTCTCCGCCTCCCAAGTAGCTGGT T G SCAP Ensembl:ENSG00000114650 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1047317297 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112004,RMVar_hsa_circ_217598,RMVar_hsa_circ_101506,RMVar_hsa_circ_217617,RMVar_hsa_circ_217618,RMVar_hsa_circ_217619 29162 RMVar_ID_29162 Human_SNP_ID_132001290 A-to-I Human chr3 - 47463970 47463970 47463970 TAAATTAGCCAGATGTGGTGGCTCATGCCTGTAGTCCCAGCAGTGTGAGAGGCTGAGATGGGAGG TAAATTAGCCAGATGTGGTGGCTCATGCCTGTGGTCCCAGCAGTGTGAGAGGCTGAGATGGGAGG T C SCAP Ensembl:ENSG00000114650 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1401336089 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112004,RMVar_hsa_circ_217598,RMVar_hsa_circ_101506,RMVar_hsa_circ_217617,RMVar_hsa_circ_217618,RMVar_hsa_circ_217619 29163 RMVar_ID_29163 Human_SNP_ID_132002515 A-to-I Human chr3 - 47469103 47469103 47469103 CCTCAAGTGATCTGCCCACCTTGGCATCCCCAAGTGCTGGGATTGCAGGTGTGAGCCAACGTGCC CCTCAAGTGATCTGCCCACCTTGGCATCCCCAGGTGCTGGGATTGCAGGTGTGAGCCAACGTGCC T C SCAP Ensembl:ENSG00000114650 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs969922233 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112004,RMVar_hsa_circ_217598 29164 RMVar_ID_29164 Human_SNP_ID_132002530 A-to-I Human chr3 - 47469191 47469191 47469191 GGCATGTGCCACCACACCCGGCTAATTTTTGTATTTTTTGTAGAGATAGGGTTTCACCATGTTGG GGCATGTGCCACCACACCCGGCTAATTTTTGTGTTTTTTGTAGAGATAGGGTTTCACCATGTTGG T C SCAP Ensembl:ENSG00000114650 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1197227305 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112004,RMVar_hsa_circ_217598 29165 RMVar_ID_29165 Human_SNP_ID_132002531 A-to-I Human chr3 - 47469191 47469191 47469191 GGCATGTGCCACCACACCCGGCTAATTTTTGTATTTTTTGTAGAGATAGGGTTTCACCATGTTGG GGCATGTGCCACCACACCCGGCTAATTTTTGTCTTTTTTGTAGAGATAGGGTTTCACCATGTTGG T G SCAP Ensembl:ENSG00000114650 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1197227305 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112004,RMVar_hsa_circ_217598 29166 RMVar_ID_29166 Human_SNP_ID_132003018 A-to-I Human chr3 - 47471549 47471549 47471549 CTGACCAACATGTGTGAAACCCCGTCTCCACTATAAATACAAAAGTTAGCCAGGTGTGGTGGCAT CTGACCAACATGTGTGAAACCCCGTCTCCACTGTAAATACAAAAGTTAGCCAGGTGTGGTGGCAT T C SCAP Ensembl:ENSG00000114650 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1269034387 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112004,RMVar_hsa_circ_217598 29167 RMVar_ID_29167 Human_SNP_ID_132007785 A-to-I Human chr3 - 47488780 47488780 47488780 TGCAGTGAGATGCTGTCCTATTTTTTTGAGACAGTCTTGCTTTGTCACCCATGCTGAAGTGCAGC TGCAGTGAGATGCTGTCCTATTTTTTTGAGACCGTCTTGCTTTGTCACCCATGCTGAAGTGCAGC T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1168118279 Functional Loss SNV dbSNP153 33..33 33 - - - 29168 RMVar_ID_29168 Human_SNP_ID_132007786 A-to-I Human chr3 - 47488782 47488782 47488782 GATGCAGTGAGATGCTGTCCTATTTTTTTGAGACAGTCTTGCTTTGTCACCCATGCTGAAGTGCA GATGCAGTGAGATGCTGTCCTATTTTTTTGAGCCAGTCTTGCTTTGTCACCCATGCTGAAGTGCA T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348052813 Functional Loss SNV dbSNP153 33..33 33 - - - 29169 RMVar_ID_29169 Human_SNP_ID_132008107 A-to-I Human chr3 - 47489931 47489931 47489931 ATACAAAAGTTAGGGCATGGTGGCACACGCCTATAGTCCCAGCTACTCAGGAGGCTGAGGCAGGG ATACAAAAGTTAGGGCATGGTGGCACACGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGG T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs980123977 Functional Loss SNV dbSNP153 33..33 33 - - - 29170 RMVar_ID_29170 Human_SNP_ID_132010038 A-to-I Human chr3 - 47497616 47497616 47497616 CCAGCCTGTTCCTTTTACAGGTGGAGACTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGC CCAGCCTGTTCCTTTTACAGGTGGAGACTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGC T C ELP6 Ensembl:ENSG00000163832 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6762177 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118529,RMVar_hsa_circ_128056,RMVar_hsa_circ_217622,RMVar_hsa_circ_111628,RMVar_hsa_circ_217623,RMVar_hsa_circ_217621 29171 RMVar_ID_29171 Human_SNP_ID_132010058 A-to-I Human chr3 - 47497681 47497681 47497681 CGTGATCCACCCCCACCCCCCTTTGCTTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGTGC CGTGATCCACCCCCACCCCCCTTTGCTTCCCAGAGTGCTGGGATTACAGGTGTGAGCCACCGTGC T C ELP6 Ensembl:ENSG00000163832 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1042792678 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1205587 RMVar_hsa_circ_118529,RMVar_hsa_circ_128056,RMVar_hsa_circ_217622,RMVar_hsa_circ_111628,RMVar_hsa_circ_217623,RMVar_hsa_circ_217621 29172 RMVar_ID_29172 Human_SNP_ID_132010126 A-to-I Human chr3 - 47497909 47497909 47497909 CCTTTTTTTTTTAGACGGAGTCTTGCTCTGTCACCTAGGCTAGAGTGCAGTGGCGCGATCTTGGC CCTTTTTTTTTTAGACGGAGTCTTGCTCTGTCGCCTAGGCTAGAGTGCAGTGGCGCGATCTTGGC T C ELP6 Ensembl:ENSG00000163832 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1269538073 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118529,RMVar_hsa_circ_128056,RMVar_hsa_circ_217622,RMVar_hsa_circ_111628,RMVar_hsa_circ_217623,RMVar_hsa_circ_217621 29173 RMVar_ID_29173 Human_SNP_ID_132010229 A-to-I Human chr3 - 47498261 47498261 47498261 ACGGGCAGGTATGCAGGGGCCTCCTGGGCAACAGGCTTCTTGCCCGTGTACCTGTGATTCTTGAC ACGGGCAGGTATGCAGGGGCCTCCTGGGCAACTGGCTTCTTGCCCGTGTACCTGTGATTCTTGAC T A ELP6 Ensembl:ENSG00000163832 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2170814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_835517,Human_RBP_ID_933080,Human_RBP_ID_19115329 RMVar_hsa_circ_118529,RMVar_hsa_circ_128056,RMVar_hsa_circ_217622,RMVar_hsa_circ_111628,RMVar_hsa_circ_217623,RMVar_hsa_circ_217621 29174 RMVar_ID_29174 Human_SNP_ID_132010230 A-to-I Human chr3 - 47498261 47498261 47498261 ACGGGCAGGTATGCAGGGGCCTCCTGGGCAACAGGCTTCTTGCCCGTGTACCTGTGATTCTTGAC ACGGGCAGGTATGCAGGGGCCTCCTGGGCAACGGGCTTCTTGCCCGTGTACCTGTGATTCTTGAC T C ELP6 Ensembl:ENSG00000163832 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2170814 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_835517,Human_RBP_ID_933080,Human_RBP_ID_19115329 RMVar_hsa_circ_118529,RMVar_hsa_circ_128056,RMVar_hsa_circ_217622,RMVar_hsa_circ_111628,RMVar_hsa_circ_217623,RMVar_hsa_circ_217621 29175 RMVar_ID_29175 Human_SNP_ID_132010231 A-to-I Human chr3 - 47498261 47498261 47498261 ACGGGCAGGTATGCAGGGGCCTCCTGGGCAACAGGCTTCTTGCCCGTGTACCTGTGATTCTTGAC ACGGGCAGGTATGCAGGGGCCTCCTGGGCAACCGGCTTCTTGCCCGTGTACCTGTGATTCTTGAC T G ELP6 Ensembl:ENSG00000163832 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2170814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_835517,Human_RBP_ID_933080,Human_RBP_ID_19115329 RMVar_hsa_circ_118529,RMVar_hsa_circ_128056,RMVar_hsa_circ_217622,RMVar_hsa_circ_111628,RMVar_hsa_circ_217623,RMVar_hsa_circ_217621 29176 RMVar_ID_29176 Human_SNP_ID_132013721 A-to-I Human chr3 - 47512318 47512318 47512318 GTTGGCCAGGCTGGTCTGGAACTCCTGACCTCAGGTGATCCGCCCGCCTCTGCCTCCCAAAGTGC GTTGGCCAGGCTGGTCTGGAACTCCTGACCTCGGGTGATCCGCCCGCCTCTGCCTCCCAAAGTGC T C ELP6 Ensembl:ENSG00000163832 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1235346420 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128056,RMVar_hsa_circ_217623 29177 RMVar_ID_29177 Human_SNP_ID_132013731 A-to-I Human chr3 - 47512369 47512369 47512369 TACTTGGCTGATTTTTTTTTGTATTTTTTGTTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGG TACTTGGCTGATTTTTTTTTGTATTTTTTGTTGGAGACGGGGTTTCACCATGTTGGCCAGGCTGG T C ELP6 Ensembl:ENSG00000163832 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs986877460 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128056,RMVar_hsa_circ_217623 29178 RMVar_ID_29178 Human_SNP_ID_132013760 A-to-I Human chr3 - 47512488 47512488 47512488 GGAGTGCACTGGCGCGATCTCGGCTCCCTGCAACCTCACCTCCCGGGTTCAAGTGATTCTCCTTA GGAGTGCACTGGCGCGATCTCGGCTCCCTGCAGCCTCACCTCCCGGGTTCAAGTGATTCTCCTTA T C ELP6 Ensembl:ENSG00000163832 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1354852352 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14845044 RMVar_hsa_circ_128056,RMVar_hsa_circ_217623 29179 RMVar_ID_29179 Human_SNP_ID_132013955 A-to-I Human chr3 - 47513224 47513224 47513224 AGTTTGGGAGGCCGAGGCGGGTGCATCATCTAAGGTCAAGAGTTCGAGACAAGTCTGGCCAAGAT AGTTTGGGAGGCCGAGGCGGGTGCATCATCTAGGGTCAAGAGTTCGAGACAAGTCTGGCCAAGAT T C ELP6 Ensembl:ENSG00000163832 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs756031086 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_155600 Human_Splice_Rec_422769,Human_Splice_Rec_422777 RMVar_hsa_circ_128056,RMVar_hsa_circ_217623 29180 RMVar_ID_29180 Human_SNP_ID_132027464 A-to-I Human chr3 - 47567794 47567794 47567794 TTGCCCAGGCTGGTCTCGAACCCCTGGGCTCAAGTGATCTTCCTGCCGCAGCCTCCCAAAGTGTT TTGCCCAGGCTGGTCTCGAACCCCTGGGCTCAGGTGATCTTCCTGCCGCAGCCTCCCAAAGTGTT T C CSPG5 Ensembl:ENSG00000114646 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs990045932 Functional Loss SNV dbSNP153 33..33 33 - - - 29181 RMVar_ID_29181 Human_SNP_ID_132033701 A-to-I Human chr3 - 47592737 47592737 47592737 AAAATTAGCCAGGCATGGTGGTGCTCACCTGTAGTTCCAGCTACTTGAGAGGCTGAGGCAGGGGG AAAATTAGCCAGGCATGGTGGTGCTCACCTGTGGTTCCAGCTACTTGAGAGGCTGAGGCAGGGGG T C SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1343592663 Functional Loss SNV dbSNP153 33..33 33 - - - 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 29182 RMVar_ID_29182 Human_SNP_ID_132034661 A-to-I Human chr3 - 47596480 47596480 47596480 TCACTGCAACCTCCGCCTCCCACGTTCAAGCAATTCCCTGCCTCAGCCTCCCGAGTAGCTAGGAT TCACTGCAACCTCCGCCTCCCACGTTCAAGCAGTTCCCTGCCTCAGCCTCCCGAGTAGCTAGGAT T C SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1017908325 Functional Loss SNV dbSNP153 33..33 33 - - - 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 29183 RMVar_ID_29183 Human_SNP_ID_132035212 A-to-I Human chr3 - 47598595 47598595 47598595 GATCTGCTGACCTCAAGTAATCCACCCACCTCAGCCTCCCAAAGTACTGGGATTACAGGCATGAG GATCTGCTGACCTCAAGTAATCCACCCACCTCTGCCTCCCAAAGTACTGGGATTACAGGCATGAG T A SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1371205216 Functional Loss SNV dbSNP153 33..33 33 - - - 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 29184 RMVar_ID_29184 Human_SNP_ID_132035438 A-to-I Human chr3 - 47599283 47599283 47599283 TACCTCCCGGGTTCAAGTGATTCTCTTGCCTCAGCTTCCCAAGTAGCTGGTATTACAGGCATGTG TACCTCCCGGGTTCAAGTGATTCTCTTGCCTCGGCTTCCCAAGTAGCTGGTATTACAGGCATGTG T C SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs557992883 Functional Loss SNV dbSNP153 33..33 33 - - - 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 29185 RMVar_ID_29185 Human_SNP_ID_132036367 A-to-I Human chr3 - 47602984 47602984 47602984 TCTGCTCTCCATAGGCATGGATGTATTTTAGTAGAGACAAGGTCTCACTATGTTGCCCAGGTTGG TCTGCTCTCCATAGGCATGGATGTATTTTAGTGGAGACAAGGTCTCACTATGTTGCCCAGGTTGG T C AC112512.1,SMARCC1 Ensembl:ENSG00000214773,Ensembl:ENSG00000173473 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs765013526 Functional Loss SNV dbSNP153 33..33 33 - - - 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,RMVar_hsa_circ_217642 29186 RMVar_ID_29186 Human_SNP_ID_132037049 A-to-I Human chr3 - 47605673 47605665 47605674 AACCTGCCAGGCTCAAGCCATCCTCCCACCTCAGCCTCTTGAGTAGCTGGGACCACAAGTGCACA AACCTGCCAGGCTCAAGCCATCCTCCCACCT_________GAGTAGCTGGGACCACAAGTGCACA CAAGAGGCTG C SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1437381435 Functional Loss DEL dbSNP153 32..40 33 - - - 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,RMVar_hsa_circ_217642 29187 RMVar_ID_29187 Human_SNP_ID_132037066 A-to-I Human chr3 - 47605742 47605742 47605742 GACAGACAGGGCCTTACTCTGTCACCCAGGCTAGAGTGCAGTGACATTATCAGGGCTCACTGCAG GACAGACAGGGCCTTACTCTGTCACCCAGGCTGGAGTGCAGTGACATTATCAGGGCTCACTGCAG T C SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1320667724 Functional Loss SNV dbSNP153 33..33 33 - - - 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,RMVar_hsa_circ_217642 29188 RMVar_ID_29188 Human_SNP_ID_132037606 A-to-I Human chr3 - 47608241 47608241 47608241 TCTACTGAAAATACAAAAATTAGCCAGGTGTAATGGTGCACATCTGCAGTCCCATCTACTCAGGA TCTACTGAAAATACAAAAATTAGCCAGGTGTAGTGGTGCACATCTGCAGTCCCATCTACTCAGGA T C SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs939014761 Functional Loss SNV dbSNP153 33..33 33 - - - 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,RMVar_hsa_circ_217642 29189 RMVar_ID_29189 Human_SNP_ID_132044357 A-to-I Human chr3 - 47636716 47636716 47636716 AGTCTCACTCTTGCTGCCTAGGCTAGAGTGCAATGGTGTGATCTTGGGTCACTGCAATCTCTGCC AGTCTCACTCTTGCTGCCTAGGCTAGAGTGCAGTGGTGTGATCTTGGGTCACTGCAATCTCTGCC T C SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs558630633 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4009,RMVar_hsa_circ_37539,RMVar_hsa_circ_92479,RMVar_hsa_circ_265112,RMVar_hsa_circ_341042,RMVar_hsa_circ_217639,RMVar_hsa_circ_217648,RMVar_hsa_circ_95274,RMVar_hsa_circ_289575,RMVar_hsa_circ_372290,RMVar_hsa_circ_217640,RMVar_hsa_circ_217641,RMVar_hsa_circ_217642,RMVar_hsa_circ_374626,RMVar_hsa_circ_310064,RMVar_hsa_circ_318875,RMVar_hsa_circ_295679,RMVar_hsa_circ_41465,RMVar_hsa_circ_217649,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_305082,RMVar_hsa_circ_76288,RMVar_hsa_circ_284771,RMVar_hsa_circ_10281,RMVar_hsa_circ_217652,RMVar_hsa_circ_217654,RMVar_hsa_circ_217655,RMVar_hsa_circ_217653,RMVar_hsa_circ_288549,RMVar_hsa_circ_306700,RMVar_hsa_circ_358271,RMVar_hsa_circ_298299,RMVar_hsa_circ_71489,RMVar_hsa_circ_217659,RMVar_hsa_circ_217660,RMVar_hsa_circ_217661,RMVar_hsa_circ_217658,RMVar_hsa_circ_217662,RMVar_hsa_circ_87594,RMVar_hsa_circ_112149,RMVar_hsa_circ_265467,RMVar_hsa_circ_217663 29190 RMVar_ID_29190 Human_SNP_ID_132044636 A-to-I Human chr3 - 47637612 47637612 47637612 CGTTTTCTGAGTTCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGCCACGCG CGTTTTCTGAGTTCAAGCAATTCTCCTGCCTCGGCCTCCCAAGTAGCTGGGATTACAGCCACGCG T C SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs905426539 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4009,RMVar_hsa_circ_37539,RMVar_hsa_circ_92479,RMVar_hsa_circ_265112,RMVar_hsa_circ_341042,RMVar_hsa_circ_217639,RMVar_hsa_circ_217648,RMVar_hsa_circ_95274,RMVar_hsa_circ_289575,RMVar_hsa_circ_372290,RMVar_hsa_circ_217640,RMVar_hsa_circ_217641,RMVar_hsa_circ_217642,RMVar_hsa_circ_374626,RMVar_hsa_circ_310064,RMVar_hsa_circ_318875,RMVar_hsa_circ_295679,RMVar_hsa_circ_41465,RMVar_hsa_circ_217649,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_305082,RMVar_hsa_circ_76288,RMVar_hsa_circ_284771,RMVar_hsa_circ_10281,RMVar_hsa_circ_217652,RMVar_hsa_circ_217654,RMVar_hsa_circ_217655,RMVar_hsa_circ_217653,RMVar_hsa_circ_288549,RMVar_hsa_circ_306700,RMVar_hsa_circ_358271,RMVar_hsa_circ_298299,RMVar_hsa_circ_71489,RMVar_hsa_circ_217659,RMVar_hsa_circ_217660,RMVar_hsa_circ_217661,RMVar_hsa_circ_217658,RMVar_hsa_circ_217662,RMVar_hsa_circ_87594,RMVar_hsa_circ_112149,RMVar_hsa_circ_265467,RMVar_hsa_circ_217663 29191 RMVar_ID_29191 Human_SNP_ID_132044648 A-to-I Human chr3 - 47637670 47637670 47637670 TCTCACTCTGTCGCACAGGCTGGAATGCAGCAACGCAATCTTGGCTCACTGCAACCTCCGTTTTC TCTCACTCTGTCGCACAGGCTGGAATGCAGCAGCGCAATCTTGGCTCACTGCAACCTCCGTTTTC T C SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1453363923 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4009,RMVar_hsa_circ_37539,RMVar_hsa_circ_92479,RMVar_hsa_circ_265112,RMVar_hsa_circ_341042,RMVar_hsa_circ_217639,RMVar_hsa_circ_217648,RMVar_hsa_circ_95274,RMVar_hsa_circ_289575,RMVar_hsa_circ_372290,RMVar_hsa_circ_217640,RMVar_hsa_circ_217641,RMVar_hsa_circ_217642,RMVar_hsa_circ_374626,RMVar_hsa_circ_310064,RMVar_hsa_circ_318875,RMVar_hsa_circ_295679,RMVar_hsa_circ_41465,RMVar_hsa_circ_217649,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_305082,RMVar_hsa_circ_76288,RMVar_hsa_circ_284771,RMVar_hsa_circ_10281,RMVar_hsa_circ_217652,RMVar_hsa_circ_217654,RMVar_hsa_circ_217655,RMVar_hsa_circ_217653,RMVar_hsa_circ_288549,RMVar_hsa_circ_306700,RMVar_hsa_circ_358271,RMVar_hsa_circ_298299,RMVar_hsa_circ_71489,RMVar_hsa_circ_217659,RMVar_hsa_circ_217660,RMVar_hsa_circ_217661,RMVar_hsa_circ_217658,RMVar_hsa_circ_217662,RMVar_hsa_circ_87594,RMVar_hsa_circ_112149,RMVar_hsa_circ_265467,RMVar_hsa_circ_217663 29192 RMVar_ID_29192 Human_SNP_ID_132044813 A-to-I Human chr3 - 47638283 47638283 47638283 CGAGACCGTCCTGGCTAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAAAATTAGCCAGG CGAGACCGTCCTGGCTAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAAAATTAGCCAGG T C SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1256525494 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4009,RMVar_hsa_circ_37539,RMVar_hsa_circ_92479,RMVar_hsa_circ_265112,RMVar_hsa_circ_341042,RMVar_hsa_circ_217639,RMVar_hsa_circ_217648,RMVar_hsa_circ_95274,RMVar_hsa_circ_289575,RMVar_hsa_circ_372290,RMVar_hsa_circ_217640,RMVar_hsa_circ_217641,RMVar_hsa_circ_217642,RMVar_hsa_circ_374626,RMVar_hsa_circ_310064,RMVar_hsa_circ_318875,RMVar_hsa_circ_295679,RMVar_hsa_circ_41465,RMVar_hsa_circ_217649,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_305082,RMVar_hsa_circ_76288,RMVar_hsa_circ_284771,RMVar_hsa_circ_10281,RMVar_hsa_circ_217652,RMVar_hsa_circ_217654,RMVar_hsa_circ_217655,RMVar_hsa_circ_217653,RMVar_hsa_circ_288549,RMVar_hsa_circ_306700,RMVar_hsa_circ_358271,RMVar_hsa_circ_298299,RMVar_hsa_circ_71489,RMVar_hsa_circ_217659,RMVar_hsa_circ_217660,RMVar_hsa_circ_217661,RMVar_hsa_circ_217658,RMVar_hsa_circ_217662,RMVar_hsa_circ_87594,RMVar_hsa_circ_112149,RMVar_hsa_circ_265467,RMVar_hsa_circ_217663 29193 RMVar_ID_29193 Human_SNP_ID_132044815 A-to-I Human chr3 - 47638296 47638296 47638296 AAGGCCAAGAGATCGAGACCGTCCTGGCTAACATGGTGAAACCCCATCTCTACTAAAAATACAAA AAGGCCAAGAGATCGAGACCGTCCTGGCTAACGTGGTGAAACCCCATCTCTACTAAAAATACAAA T C SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1056753450 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4009,RMVar_hsa_circ_37539,RMVar_hsa_circ_92479,RMVar_hsa_circ_265112,RMVar_hsa_circ_341042,RMVar_hsa_circ_217639,RMVar_hsa_circ_217648,RMVar_hsa_circ_95274,RMVar_hsa_circ_289575,RMVar_hsa_circ_372290,RMVar_hsa_circ_217640,RMVar_hsa_circ_217641,RMVar_hsa_circ_217642,RMVar_hsa_circ_374626,RMVar_hsa_circ_310064,RMVar_hsa_circ_318875,RMVar_hsa_circ_295679,RMVar_hsa_circ_41465,RMVar_hsa_circ_217649,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_305082,RMVar_hsa_circ_76288,RMVar_hsa_circ_284771,RMVar_hsa_circ_10281,RMVar_hsa_circ_217652,RMVar_hsa_circ_217654,RMVar_hsa_circ_217655,RMVar_hsa_circ_217653,RMVar_hsa_circ_288549,RMVar_hsa_circ_306700,RMVar_hsa_circ_358271,RMVar_hsa_circ_298299,RMVar_hsa_circ_71489,RMVar_hsa_circ_217659,RMVar_hsa_circ_217660,RMVar_hsa_circ_217661,RMVar_hsa_circ_217658,RMVar_hsa_circ_217662,RMVar_hsa_circ_87594,RMVar_hsa_circ_112149,RMVar_hsa_circ_265467,RMVar_hsa_circ_217663 29194 RMVar_ID_29194 Human_SNP_ID_132045711 A-to-I Human chr3 - 47642007 47642007 47642007 CACTTTGAGAGGCAGAAGCGATTGGATCGCTTAGGGCTAGGAGTTAAGACCAGCCTGAGCATTAC CACTTTGAGAGGCAGAAGCGATTGGATCGCTTGGGGCTAGGAGTTAAGACCAGCCTGAGCATTAC T C SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1326159607 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14846967,Human_RBP_ID_18809388 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_217664,RMVar_hsa_circ_217666,RMVar_hsa_circ_217667,RMVar_hsa_circ_217665 29195 RMVar_ID_29195 Human_SNP_ID_132047770 A-to-I Human chr3 - 47650619 47650619 47650619 TAGAGACAGGGTCTCACTATGTTGCTTAGACTAGTCTCAAACTCCTGAGCTCAAGCCATCATCCC TAGAGACAGGGTCTCACTATGTTGCTTAGACTCGTCTCAAACTCCTGAGCTCAAGCCATCATCCC T G SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1003150272 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14847374 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_217664,RMVar_hsa_circ_217666,RMVar_hsa_circ_217667,RMVar_hsa_circ_217665 29196 RMVar_ID_29196 Human_SNP_ID_132047776 A-to-I Human chr3 - 47650644 47650644 47650644 CCCTGGCTAATTCTTTTAGTTATTGTAGAGACAGGGTCTCACTATGTTGCTTAGACTAGTCTCAA CCCTGGCTAATTCTTTTAGTTATTGTAGAGACCGGGTCTCACTATGTTGCTTAGACTAGTCTCAA T G SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1198664844 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14847380 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_217664,RMVar_hsa_circ_217666,RMVar_hsa_circ_217667,RMVar_hsa_circ_217665 29197 RMVar_ID_29197 Human_SNP_ID_132059033 A-to-I Human chr3 - 47694429 47694429 47694429 TGCCCAGCTAGTTTTTGTATTTTAGTACAGACAGAATTTCACCATGTTGGCCAAGCTGGTCTAAG TGCCCAGCTAGTTTTTGTATTTTAGTACAGACGGAATTTCACCATGTTGGCCAAGCTGGTCTAAG T C SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1328591083 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14849149 RMVar_hsa_circ_19280,RMVar_hsa_circ_92479,RMVar_hsa_circ_217639,RMVar_hsa_circ_95274,RMVar_hsa_circ_372290,RMVar_hsa_circ_217644,RMVar_hsa_circ_217643,RMVar_hsa_circ_12057,RMVar_hsa_circ_217662,RMVar_hsa_circ_87594,RMVar_hsa_circ_116349,RMVar_hsa_circ_72594,RMVar_hsa_circ_217667,RMVar_hsa_circ_367020,RMVar_hsa_circ_217670,RMVar_hsa_circ_266920,RMVar_hsa_circ_40819,RMVar_hsa_circ_217682,RMVar_hsa_circ_87210,RMVar_hsa_circ_322764,RMVar_hsa_circ_370688,RMVar_hsa_circ_68694,RMVar_hsa_circ_217683,RMVar_hsa_circ_373618,RMVar_hsa_circ_217681,RMVar_hsa_circ_370140,RMVar_hsa_circ_338642,RMVar_hsa_circ_85311,RMVar_hsa_circ_38017,RMVar_hsa_circ_92950,RMVar_hsa_circ_217689,RMVar_hsa_circ_217690,RMVar_hsa_circ_217687,RMVar_hsa_circ_217688,RMVar_hsa_circ_217698,RMVar_hsa_circ_347090,RMVar_hsa_circ_360616,RMVar_hsa_circ_356713,RMVar_hsa_circ_319724,RMVar_hsa_circ_284507,RMVar_hsa_circ_81356,RMVar_hsa_circ_82592,RMVar_hsa_circ_217699,RMVar_hsa_circ_217701,RMVar_hsa_circ_217700,RMVar_hsa_circ_116771,RMVar_hsa_circ_295647,RMVar_hsa_circ_357551,RMVar_hsa_circ_118481,RMVar_hsa_circ_59472,RMVar_hsa_circ_217708,RMVar_hsa_circ_217709,RMVar_hsa_circ_217707,RMVar_hsa_circ_341802,RMVar_hsa_circ_365023,RMVar_hsa_circ_366507,RMVar_hsa_circ_345189,RMVar_hsa_circ_64874,RMVar_hsa_circ_217714,RMVar_hsa_circ_53009,RMVar_hsa_circ_65535,RMVar_hsa_circ_217715,RMVar_hsa_circ_217717,RMVar_hsa_circ_338301,RMVar_hsa_circ_376891,RMVar_hsa_circ_343563,RMVar_hsa_circ_269345,RMVar_hsa_circ_365424,RMVar_hsa_circ_217716,RMVar_hsa_circ_292059,RMVar_hsa_circ_217718,RMVar_hsa_circ_58202 29198 RMVar_ID_29198 Human_SNP_ID_132059062 A-to-I Human chr3 - 47694537 47694537 47694537 GGAATGCAGTGGTGCGATCTCAGCTCATTGCAACTTCCACCTCCCGGGTTCAAGTGATTCTCTTG GGAATGCAGTGGTGCGATCTCAGCTCATTGCAGCTTCCACCTCCCGGGTTCAAGTGATTCTCTTG T C SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935496602 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19280,RMVar_hsa_circ_92479,RMVar_hsa_circ_217639,RMVar_hsa_circ_95274,RMVar_hsa_circ_372290,RMVar_hsa_circ_217644,RMVar_hsa_circ_217643,RMVar_hsa_circ_12057,RMVar_hsa_circ_217662,RMVar_hsa_circ_87594,RMVar_hsa_circ_116349,RMVar_hsa_circ_72594,RMVar_hsa_circ_217667,RMVar_hsa_circ_367020,RMVar_hsa_circ_217670,RMVar_hsa_circ_266920,RMVar_hsa_circ_40819,RMVar_hsa_circ_217682,RMVar_hsa_circ_87210,RMVar_hsa_circ_322764,RMVar_hsa_circ_370688,RMVar_hsa_circ_68694,RMVar_hsa_circ_217683,RMVar_hsa_circ_373618,RMVar_hsa_circ_217681,RMVar_hsa_circ_370140,RMVar_hsa_circ_338642,RMVar_hsa_circ_85311,RMVar_hsa_circ_38017,RMVar_hsa_circ_92950,RMVar_hsa_circ_217689,RMVar_hsa_circ_217690,RMVar_hsa_circ_217687,RMVar_hsa_circ_217688,RMVar_hsa_circ_217698,RMVar_hsa_circ_347090,RMVar_hsa_circ_360616,RMVar_hsa_circ_356713,RMVar_hsa_circ_319724,RMVar_hsa_circ_284507,RMVar_hsa_circ_81356,RMVar_hsa_circ_82592,RMVar_hsa_circ_217699,RMVar_hsa_circ_217701,RMVar_hsa_circ_217700,RMVar_hsa_circ_116771,RMVar_hsa_circ_295647,RMVar_hsa_circ_357551,RMVar_hsa_circ_118481,RMVar_hsa_circ_59472,RMVar_hsa_circ_217708,RMVar_hsa_circ_217709,RMVar_hsa_circ_217707,RMVar_hsa_circ_341802,RMVar_hsa_circ_365023,RMVar_hsa_circ_366507,RMVar_hsa_circ_345189,RMVar_hsa_circ_64874,RMVar_hsa_circ_217714,RMVar_hsa_circ_53009,RMVar_hsa_circ_65535,RMVar_hsa_circ_217715,RMVar_hsa_circ_217717,RMVar_hsa_circ_338301,RMVar_hsa_circ_376891,RMVar_hsa_circ_343563,RMVar_hsa_circ_269345,RMVar_hsa_circ_365424,RMVar_hsa_circ_217716,RMVar_hsa_circ_292059,RMVar_hsa_circ_217718,RMVar_hsa_circ_58202 29199 RMVar_ID_29199 Human_SNP_ID_132061315 A-to-I Human chr3 - 47702870 47702870 47702870 TTTGGGCCAGGAGCCAGTGGCTCTTGCCTGCAATCCCAGCACTTTGGGAGGCCAAGGTAGGAGGA TTTGGGCCAGGAGCCAGTGGCTCTTGCCTGCAGTCCCAGCACTTTGGGAGGCCAAGGTAGGAGGA T C SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1270340498 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19280,RMVar_hsa_circ_92479,RMVar_hsa_circ_217639,RMVar_hsa_circ_95274,RMVar_hsa_circ_372290,RMVar_hsa_circ_217644,RMVar_hsa_circ_217643,RMVar_hsa_circ_12057,RMVar_hsa_circ_217662,RMVar_hsa_circ_87594,RMVar_hsa_circ_116349,RMVar_hsa_circ_72594,RMVar_hsa_circ_217667,RMVar_hsa_circ_367020,RMVar_hsa_circ_217670,RMVar_hsa_circ_266920,RMVar_hsa_circ_40819,RMVar_hsa_circ_217682,RMVar_hsa_circ_87210,RMVar_hsa_circ_370688,RMVar_hsa_circ_68694,RMVar_hsa_circ_373618,RMVar_hsa_circ_217681,RMVar_hsa_circ_370140,RMVar_hsa_circ_338642,RMVar_hsa_circ_85311,RMVar_hsa_circ_38017,RMVar_hsa_circ_92950,RMVar_hsa_circ_217689,RMVar_hsa_circ_217687,RMVar_hsa_circ_217688,RMVar_hsa_circ_217698,RMVar_hsa_circ_347090,RMVar_hsa_circ_360616,RMVar_hsa_circ_356713,RMVar_hsa_circ_319724,RMVar_hsa_circ_81356,RMVar_hsa_circ_217720,RMVar_hsa_circ_82592,RMVar_hsa_circ_217699,RMVar_hsa_circ_217700,RMVar_hsa_circ_116771,RMVar_hsa_circ_357551,RMVar_hsa_circ_118481,RMVar_hsa_circ_59472,RMVar_hsa_circ_217708,RMVar_hsa_circ_217709,RMVar_hsa_circ_217707,RMVar_hsa_circ_365023,RMVar_hsa_circ_366507,RMVar_hsa_circ_345189,RMVar_hsa_circ_64874,RMVar_hsa_circ_53009,RMVar_hsa_circ_65535,RMVar_hsa_circ_217715,RMVar_hsa_circ_217717,RMVar_hsa_circ_338301,RMVar_hsa_circ_376891,RMVar_hsa_circ_269345,RMVar_hsa_circ_365424,RMVar_hsa_circ_56523,RMVar_hsa_circ_330053,RMVar_hsa_circ_58202,RMVar_hsa_circ_351898,RMVar_hsa_circ_369594,RMVar_hsa_circ_339305,RMVar_hsa_circ_319610,RMVar_hsa_circ_322359,RMVar_hsa_circ_298687,RMVar_hsa_circ_217722,RMVar_hsa_circ_217724,RMVar_hsa_circ_48814,RMVar_hsa_circ_217723,RMVar_hsa_circ_217721,RMVar_hsa_circ_217719 29200 RMVar_ID_29200 Human_SNP_ID_132061462 A-to-I Human chr3 - 47703391 47703391 47703391 CATCTGCTGAGGAATAAATGAATAAAAATAATAATTAAAACAAGACAGTGCTTCAGGATGCAGAA CATCTGCTGAGGAATAAATGAATAAAAATAATGATTAAAACAAGACAGTGCTTCAGGATGCAGAA T C SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1559649328 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19280,RMVar_hsa_circ_92479,RMVar_hsa_circ_217639,RMVar_hsa_circ_95274,RMVar_hsa_circ_372290,RMVar_hsa_circ_217644,RMVar_hsa_circ_217643,RMVar_hsa_circ_12057,RMVar_hsa_circ_217662,RMVar_hsa_circ_87594,RMVar_hsa_circ_116349,RMVar_hsa_circ_72594,RMVar_hsa_circ_217667,RMVar_hsa_circ_367020,RMVar_hsa_circ_217670,RMVar_hsa_circ_266920,RMVar_hsa_circ_40819,RMVar_hsa_circ_217682,RMVar_hsa_circ_87210,RMVar_hsa_circ_370688,RMVar_hsa_circ_68694,RMVar_hsa_circ_373618,RMVar_hsa_circ_217681,RMVar_hsa_circ_370140,RMVar_hsa_circ_338642,RMVar_hsa_circ_85311,RMVar_hsa_circ_38017,RMVar_hsa_circ_92950,RMVar_hsa_circ_217689,RMVar_hsa_circ_217687,RMVar_hsa_circ_217688,RMVar_hsa_circ_217698,RMVar_hsa_circ_347090,RMVar_hsa_circ_360616,RMVar_hsa_circ_356713,RMVar_hsa_circ_319724,RMVar_hsa_circ_81356,RMVar_hsa_circ_217720,RMVar_hsa_circ_82592,RMVar_hsa_circ_217699,RMVar_hsa_circ_217700,RMVar_hsa_circ_116771,RMVar_hsa_circ_357551,RMVar_hsa_circ_118481,RMVar_hsa_circ_59472,RMVar_hsa_circ_217708,RMVar_hsa_circ_217709,RMVar_hsa_circ_217707,RMVar_hsa_circ_365023,RMVar_hsa_circ_366507,RMVar_hsa_circ_345189,RMVar_hsa_circ_64874,RMVar_hsa_circ_53009,RMVar_hsa_circ_65535,RMVar_hsa_circ_217715,RMVar_hsa_circ_217717,RMVar_hsa_circ_338301,RMVar_hsa_circ_376891,RMVar_hsa_circ_269345,RMVar_hsa_circ_365424,RMVar_hsa_circ_56523,RMVar_hsa_circ_330053,RMVar_hsa_circ_58202,RMVar_hsa_circ_351898,RMVar_hsa_circ_369594,RMVar_hsa_circ_339305,RMVar_hsa_circ_319610,RMVar_hsa_circ_322359,RMVar_hsa_circ_298687,RMVar_hsa_circ_217722,RMVar_hsa_circ_217724,RMVar_hsa_circ_48814,RMVar_hsa_circ_217723,RMVar_hsa_circ_217721,RMVar_hsa_circ_217719 29201 RMVar_ID_29201 Human_SNP_ID_132062818 A-to-I Human chr3 - 47708279 47708279 47708279 AAAATTAGCTGGGCATGGTGGTGCGCAACTGTAGTCCCAGCTACATGGGAGGCTGAGGTGAGGGG AAAATTAGCTGGGCATGGTGGTGCGCAACTGTTGTCCCAGCTACATGGGAGGCTGAGGTGAGGGG T A SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1450075753 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7201675 RMVar_hsa_circ_19280,RMVar_hsa_circ_92479,RMVar_hsa_circ_217639,RMVar_hsa_circ_95274,RMVar_hsa_circ_372290,RMVar_hsa_circ_217644,RMVar_hsa_circ_217643,RMVar_hsa_circ_12057,RMVar_hsa_circ_217662,RMVar_hsa_circ_87594,RMVar_hsa_circ_116349,RMVar_hsa_circ_72594,RMVar_hsa_circ_217667,RMVar_hsa_circ_367020,RMVar_hsa_circ_217670,RMVar_hsa_circ_266920,RMVar_hsa_circ_40819,RMVar_hsa_circ_217682,RMVar_hsa_circ_87210,RMVar_hsa_circ_370688,RMVar_hsa_circ_68694,RMVar_hsa_circ_373618,RMVar_hsa_circ_217681,RMVar_hsa_circ_370140,RMVar_hsa_circ_338642,RMVar_hsa_circ_85311,RMVar_hsa_circ_38017,RMVar_hsa_circ_92950,RMVar_hsa_circ_217689,RMVar_hsa_circ_217687,RMVar_hsa_circ_217688,RMVar_hsa_circ_217698,RMVar_hsa_circ_347090,RMVar_hsa_circ_356713,RMVar_hsa_circ_319724,RMVar_hsa_circ_81356,RMVar_hsa_circ_217720,RMVar_hsa_circ_82592,RMVar_hsa_circ_217699,RMVar_hsa_circ_217700,RMVar_hsa_circ_116771,RMVar_hsa_circ_357551,RMVar_hsa_circ_118481,RMVar_hsa_circ_217708,RMVar_hsa_circ_217709,RMVar_hsa_circ_217707,RMVar_hsa_circ_365023,RMVar_hsa_circ_366507,RMVar_hsa_circ_53009,RMVar_hsa_circ_65535,RMVar_hsa_circ_217715,RMVar_hsa_circ_217717,RMVar_hsa_circ_338301,RMVar_hsa_circ_376891,RMVar_hsa_circ_269345,RMVar_hsa_circ_365424,RMVar_hsa_circ_56523,RMVar_hsa_circ_58202,RMVar_hsa_circ_351898,RMVar_hsa_circ_369594,RMVar_hsa_circ_339305,RMVar_hsa_circ_319610,RMVar_hsa_circ_322359,RMVar_hsa_circ_298687,RMVar_hsa_circ_217722,RMVar_hsa_circ_48814,RMVar_hsa_circ_217723,RMVar_hsa_circ_217721,RMVar_hsa_circ_217731,RMVar_hsa_circ_285271,RMVar_hsa_circ_305077,RMVar_hsa_circ_308862,RMVar_hsa_circ_217719,RMVar_hsa_circ_318645,RMVar_hsa_circ_305405,RMVar_hsa_circ_293732,RMVar_hsa_circ_284010,RMVar_hsa_circ_217732,RMVar_hsa_circ_217727,RMVar_hsa_circ_217729,RMVar_hsa_circ_217730,RMVar_hsa_circ_217728,RMVar_hsa_circ_217725,RMVar_hsa_circ_217726 29202 RMVar_ID_29202 Human_SNP_ID_132063001 A-to-I Human chr3 - 47709078 47709078 47709078 TTTTTTATTTTCAGTAGAGATGGAGTTTCACTATGTTGGCCAGGCTGATCTTGAACTTCTGACCT TTTTTTATTTTCAGTAGAGATGGAGTTTCACTGTGTTGGCCAGGCTGATCTTGAACTTCTGACCT T C SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs374689222 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19280,RMVar_hsa_circ_92479,RMVar_hsa_circ_217639,RMVar_hsa_circ_95274,RMVar_hsa_circ_372290,RMVar_hsa_circ_217644,RMVar_hsa_circ_217643,RMVar_hsa_circ_12057,RMVar_hsa_circ_217662,RMVar_hsa_circ_87594,RMVar_hsa_circ_116349,RMVar_hsa_circ_72594,RMVar_hsa_circ_217667,RMVar_hsa_circ_367020,RMVar_hsa_circ_217670,RMVar_hsa_circ_266920,RMVar_hsa_circ_40819,RMVar_hsa_circ_217682,RMVar_hsa_circ_87210,RMVar_hsa_circ_370688,RMVar_hsa_circ_68694,RMVar_hsa_circ_373618,RMVar_hsa_circ_217681,RMVar_hsa_circ_370140,RMVar_hsa_circ_338642,RMVar_hsa_circ_85311,RMVar_hsa_circ_38017,RMVar_hsa_circ_92950,RMVar_hsa_circ_217689,RMVar_hsa_circ_217687,RMVar_hsa_circ_217688,RMVar_hsa_circ_217698,RMVar_hsa_circ_347090,RMVar_hsa_circ_356713,RMVar_hsa_circ_319724,RMVar_hsa_circ_81356,RMVar_hsa_circ_217720,RMVar_hsa_circ_82592,RMVar_hsa_circ_217699,RMVar_hsa_circ_217700,RMVar_hsa_circ_116771,RMVar_hsa_circ_357551,RMVar_hsa_circ_118481,RMVar_hsa_circ_217708,RMVar_hsa_circ_217709,RMVar_hsa_circ_217707,RMVar_hsa_circ_365023,RMVar_hsa_circ_366507,RMVar_hsa_circ_53009,RMVar_hsa_circ_65535,RMVar_hsa_circ_217715,RMVar_hsa_circ_217717,RMVar_hsa_circ_338301,RMVar_hsa_circ_376891,RMVar_hsa_circ_269345,RMVar_hsa_circ_365424,RMVar_hsa_circ_56523,RMVar_hsa_circ_58202,RMVar_hsa_circ_351898,RMVar_hsa_circ_369594,RMVar_hsa_circ_339305,RMVar_hsa_circ_319610,RMVar_hsa_circ_322359,RMVar_hsa_circ_298687,RMVar_hsa_circ_217722,RMVar_hsa_circ_48814,RMVar_hsa_circ_217723,RMVar_hsa_circ_217721,RMVar_hsa_circ_217731,RMVar_hsa_circ_285271,RMVar_hsa_circ_305077,RMVar_hsa_circ_308862,RMVar_hsa_circ_217719,RMVar_hsa_circ_318645,RMVar_hsa_circ_305405,RMVar_hsa_circ_293732,RMVar_hsa_circ_284010,RMVar_hsa_circ_217732,RMVar_hsa_circ_217727,RMVar_hsa_circ_217729,RMVar_hsa_circ_217730,RMVar_hsa_circ_217728,RMVar_hsa_circ_217725,RMVar_hsa_circ_217726 29203 RMVar_ID_29203 Human_SNP_ID_132064700 A-to-I Human chr3 - 47716234 47716234 47716234 TTTGTATTTTTTAATAGAAACGGGATTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTTATAC TTTGTATTTTTTAATAGAAACGGGATTTCACCGTGTTGGCCAGGCTGGTCTTGAACTCCTTATAC T C SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs893995950 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19280,RMVar_hsa_circ_92479,RMVar_hsa_circ_217639,RMVar_hsa_circ_95274,RMVar_hsa_circ_372290,RMVar_hsa_circ_217644,RMVar_hsa_circ_217643,RMVar_hsa_circ_12057,RMVar_hsa_circ_217662,RMVar_hsa_circ_87594,RMVar_hsa_circ_72594,RMVar_hsa_circ_367020,RMVar_hsa_circ_217670,RMVar_hsa_circ_40819,RMVar_hsa_circ_370688,RMVar_hsa_circ_68694,RMVar_hsa_circ_373618,RMVar_hsa_circ_217681,RMVar_hsa_circ_338642,RMVar_hsa_circ_85311,RMVar_hsa_circ_38017,RMVar_hsa_circ_92950,RMVar_hsa_circ_217687,RMVar_hsa_circ_217688,RMVar_hsa_circ_217698,RMVar_hsa_circ_347090,RMVar_hsa_circ_319724,RMVar_hsa_circ_81356,RMVar_hsa_circ_217720,RMVar_hsa_circ_217699,RMVar_hsa_circ_217700,RMVar_hsa_circ_116771,RMVar_hsa_circ_357551,RMVar_hsa_circ_118481,RMVar_hsa_circ_217708,RMVar_hsa_circ_217709,RMVar_hsa_circ_217707,RMVar_hsa_circ_365023,RMVar_hsa_circ_366507,RMVar_hsa_circ_53009,RMVar_hsa_circ_65535,RMVar_hsa_circ_217717,RMVar_hsa_circ_338301,RMVar_hsa_circ_376891,RMVar_hsa_circ_269345,RMVar_hsa_circ_365424,RMVar_hsa_circ_56523,RMVar_hsa_circ_58202,RMVar_hsa_circ_351898,RMVar_hsa_circ_369594,RMVar_hsa_circ_339305,RMVar_hsa_circ_319610,RMVar_hsa_circ_322359,RMVar_hsa_circ_217722,RMVar_hsa_circ_217721,RMVar_hsa_circ_112692,RMVar_hsa_circ_285271,RMVar_hsa_circ_308862,RMVar_hsa_circ_217719,RMVar_hsa_circ_318645,RMVar_hsa_circ_293732,RMVar_hsa_circ_284010,RMVar_hsa_circ_217727,RMVar_hsa_circ_217729,RMVar_hsa_circ_217728,RMVar_hsa_circ_217735,RMVar_hsa_circ_217725,RMVar_hsa_circ_217726,RMVar_hsa_circ_285186,RMVar_hsa_circ_358616,RMVar_hsa_circ_307690,RMVar_hsa_circ_69873,RMVar_hsa_circ_299391,RMVar_hsa_circ_306145,RMVar_hsa_circ_361583,RMVar_hsa_circ_299759,RMVar_hsa_circ_279029,RMVar_hsa_circ_217737,RMVar_hsa_circ_217739,RMVar_hsa_circ_217740,RMVar_hsa_circ_217738,RMVar_hsa_circ_217736 29204 RMVar_ID_29204 Human_SNP_ID_132064706 A-to-I Human chr3 - 47716248 47716248 47716248 ACGCCCCGCTAATTTTTGTATTTTTTAATAGAAACGGGATTTCACCATGTTGGCCAGGCTGGTCT ACGCCCCGCTAATTTTTGTATTTTTTAATAGACACGGGATTTCACCATGTTGGCCAGGCTGGTCT T G SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs560050945 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19280,RMVar_hsa_circ_92479,RMVar_hsa_circ_217639,RMVar_hsa_circ_95274,RMVar_hsa_circ_372290,RMVar_hsa_circ_217644,RMVar_hsa_circ_217643,RMVar_hsa_circ_12057,RMVar_hsa_circ_217662,RMVar_hsa_circ_87594,RMVar_hsa_circ_72594,RMVar_hsa_circ_367020,RMVar_hsa_circ_217670,RMVar_hsa_circ_40819,RMVar_hsa_circ_370688,RMVar_hsa_circ_68694,RMVar_hsa_circ_373618,RMVar_hsa_circ_217681,RMVar_hsa_circ_338642,RMVar_hsa_circ_85311,RMVar_hsa_circ_38017,RMVar_hsa_circ_92950,RMVar_hsa_circ_217687,RMVar_hsa_circ_217688,RMVar_hsa_circ_217698,RMVar_hsa_circ_347090,RMVar_hsa_circ_319724,RMVar_hsa_circ_81356,RMVar_hsa_circ_217720,RMVar_hsa_circ_217699,RMVar_hsa_circ_217700,RMVar_hsa_circ_116771,RMVar_hsa_circ_357551,RMVar_hsa_circ_118481,RMVar_hsa_circ_217708,RMVar_hsa_circ_217709,RMVar_hsa_circ_217707,RMVar_hsa_circ_365023,RMVar_hsa_circ_366507,RMVar_hsa_circ_53009,RMVar_hsa_circ_65535,RMVar_hsa_circ_217717,RMVar_hsa_circ_338301,RMVar_hsa_circ_376891,RMVar_hsa_circ_269345,RMVar_hsa_circ_365424,RMVar_hsa_circ_56523,RMVar_hsa_circ_58202,RMVar_hsa_circ_351898,RMVar_hsa_circ_369594,RMVar_hsa_circ_339305,RMVar_hsa_circ_319610,RMVar_hsa_circ_322359,RMVar_hsa_circ_217722,RMVar_hsa_circ_217721,RMVar_hsa_circ_112692,RMVar_hsa_circ_285271,RMVar_hsa_circ_308862,RMVar_hsa_circ_217719,RMVar_hsa_circ_318645,RMVar_hsa_circ_293732,RMVar_hsa_circ_284010,RMVar_hsa_circ_217727,RMVar_hsa_circ_217729,RMVar_hsa_circ_217728,RMVar_hsa_circ_217735,RMVar_hsa_circ_217725,RMVar_hsa_circ_217726,RMVar_hsa_circ_285186,RMVar_hsa_circ_358616,RMVar_hsa_circ_307690,RMVar_hsa_circ_69873,RMVar_hsa_circ_299391,RMVar_hsa_circ_306145,RMVar_hsa_circ_361583,RMVar_hsa_circ_299759,RMVar_hsa_circ_279029,RMVar_hsa_circ_217737,RMVar_hsa_circ_217739,RMVar_hsa_circ_217740,RMVar_hsa_circ_217738,RMVar_hsa_circ_217736 29205 RMVar_ID_29205 Human_SNP_ID_132064721 A-to-I Human chr3 - 47716309 47716309 47716309 GGTTCATGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGAGATTACAGGTGCACACTACAACGC GGTTCATGCGATTCTCCTGCCTCAGCCTCCCACGTAGCTGAGATTACAGGTGCACACTACAACGC T G SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1344694071 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19280,RMVar_hsa_circ_92479,RMVar_hsa_circ_217639,RMVar_hsa_circ_95274,RMVar_hsa_circ_372290,RMVar_hsa_circ_217644,RMVar_hsa_circ_217643,RMVar_hsa_circ_12057,RMVar_hsa_circ_217662,RMVar_hsa_circ_87594,RMVar_hsa_circ_72594,RMVar_hsa_circ_367020,RMVar_hsa_circ_217670,RMVar_hsa_circ_40819,RMVar_hsa_circ_370688,RMVar_hsa_circ_68694,RMVar_hsa_circ_373618,RMVar_hsa_circ_217681,RMVar_hsa_circ_338642,RMVar_hsa_circ_85311,RMVar_hsa_circ_38017,RMVar_hsa_circ_92950,RMVar_hsa_circ_217687,RMVar_hsa_circ_217688,RMVar_hsa_circ_217698,RMVar_hsa_circ_347090,RMVar_hsa_circ_319724,RMVar_hsa_circ_81356,RMVar_hsa_circ_217720,RMVar_hsa_circ_217699,RMVar_hsa_circ_217700,RMVar_hsa_circ_116771,RMVar_hsa_circ_357551,RMVar_hsa_circ_118481,RMVar_hsa_circ_217708,RMVar_hsa_circ_217709,RMVar_hsa_circ_217707,RMVar_hsa_circ_365023,RMVar_hsa_circ_366507,RMVar_hsa_circ_53009,RMVar_hsa_circ_65535,RMVar_hsa_circ_217717,RMVar_hsa_circ_338301,RMVar_hsa_circ_376891,RMVar_hsa_circ_269345,RMVar_hsa_circ_365424,RMVar_hsa_circ_56523,RMVar_hsa_circ_58202,RMVar_hsa_circ_351898,RMVar_hsa_circ_369594,RMVar_hsa_circ_339305,RMVar_hsa_circ_319610,RMVar_hsa_circ_322359,RMVar_hsa_circ_217722,RMVar_hsa_circ_217721,RMVar_hsa_circ_112692,RMVar_hsa_circ_285271,RMVar_hsa_circ_308862,RMVar_hsa_circ_217719,RMVar_hsa_circ_318645,RMVar_hsa_circ_293732,RMVar_hsa_circ_284010,RMVar_hsa_circ_217727,RMVar_hsa_circ_217729,RMVar_hsa_circ_217728,RMVar_hsa_circ_217735,RMVar_hsa_circ_217725,RMVar_hsa_circ_217726,RMVar_hsa_circ_285186,RMVar_hsa_circ_358616,RMVar_hsa_circ_307690,RMVar_hsa_circ_69873,RMVar_hsa_circ_299391,RMVar_hsa_circ_306145,RMVar_hsa_circ_361583,RMVar_hsa_circ_299759,RMVar_hsa_circ_279029,RMVar_hsa_circ_217737,RMVar_hsa_circ_217739,RMVar_hsa_circ_217740,RMVar_hsa_circ_217738,RMVar_hsa_circ_217736 29206 RMVar_ID_29206 Human_SNP_ID_132066076 A-to-I Human chr3 - 47721846 47721846 47721846 CTAGCTATTTACTTTTATTTTTAAAATTTTTTAAGAGACTGAATCTCACTTTGTTGCCCAGGGTG CTAGCTATTTACTTTTATTTTTAAAATTTTTTCAGAGACTGAATCTCACTTTGTTGCCCAGGGTG T G SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1046628851 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7201733,Human_RBP_ID_14849687 RMVar_hsa_circ_19280,RMVar_hsa_circ_92479,RMVar_hsa_circ_217639,RMVar_hsa_circ_95274,RMVar_hsa_circ_372290,RMVar_hsa_circ_217644,RMVar_hsa_circ_217643,RMVar_hsa_circ_217662,RMVar_hsa_circ_87594,RMVar_hsa_circ_72594,RMVar_hsa_circ_40819,RMVar_hsa_circ_370688,RMVar_hsa_circ_68694,RMVar_hsa_circ_217681,RMVar_hsa_circ_338642,RMVar_hsa_circ_85311,RMVar_hsa_circ_38017,RMVar_hsa_circ_92950,RMVar_hsa_circ_217687,RMVar_hsa_circ_217698,RMVar_hsa_circ_347090,RMVar_hsa_circ_319724,RMVar_hsa_circ_81356,RMVar_hsa_circ_217720,RMVar_hsa_circ_217699,RMVar_hsa_circ_217700,RMVar_hsa_circ_357551,RMVar_hsa_circ_118481,RMVar_hsa_circ_217708,RMVar_hsa_circ_217707,RMVar_hsa_circ_366507,RMVar_hsa_circ_53009,RMVar_hsa_circ_65535,RMVar_hsa_circ_217717,RMVar_hsa_circ_338301,RMVar_hsa_circ_376891,RMVar_hsa_circ_269345,RMVar_hsa_circ_365424,RMVar_hsa_circ_56523,RMVar_hsa_circ_369594,RMVar_hsa_circ_339305,RMVar_hsa_circ_319610,RMVar_hsa_circ_322359,RMVar_hsa_circ_217721,RMVar_hsa_circ_112692,RMVar_hsa_circ_285271,RMVar_hsa_circ_217719,RMVar_hsa_circ_318645,RMVar_hsa_circ_293732,RMVar_hsa_circ_284010,RMVar_hsa_circ_217727,RMVar_hsa_circ_217735,RMVar_hsa_circ_217725,RMVar_hsa_circ_217726,RMVar_hsa_circ_285186,RMVar_hsa_circ_307690,RMVar_hsa_circ_69873,RMVar_hsa_circ_299391,RMVar_hsa_circ_306145,RMVar_hsa_circ_361583,RMVar_hsa_circ_299759,RMVar_hsa_circ_279029,RMVar_hsa_circ_217742,RMVar_hsa_circ_122716,RMVar_hsa_circ_322115,RMVar_hsa_circ_217737,RMVar_hsa_circ_217739,RMVar_hsa_circ_217740,RMVar_hsa_circ_217738,RMVar_hsa_circ_217736,RMVar_hsa_circ_369776,RMVar_hsa_circ_276995,RMVar_hsa_circ_277214,RMVar_hsa_circ_273166,RMVar_hsa_circ_217746,RMVar_hsa_circ_217748,RMVar_hsa_circ_217747,RMVar_hsa_circ_217744,RMVar_hsa_circ_217745,RMVar_hsa_circ_217743,RMVar_hsa_circ_217741 29207 RMVar_ID_29207 Human_SNP_ID_132066516 A-to-I Human chr3 - 47723473 47723473 47723473 CAGTTGTAGGCCTTTTAAATTTTTTTTTTTTTAAGACAGAATTTCATTCCGTCACCCTGGCTGGT CAGTTGTAGGCCTTTTAAATTTTTTTTTTTTTGAGACAGAATTTCATTCCGTCACCCTGGCTGGT T C SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs542593031 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14849732,Human_RBP_ID_21939200 RMVar_hsa_circ_19280,RMVar_hsa_circ_92479,RMVar_hsa_circ_217639,RMVar_hsa_circ_95274,RMVar_hsa_circ_372290,RMVar_hsa_circ_217644,RMVar_hsa_circ_217643,RMVar_hsa_circ_217662,RMVar_hsa_circ_87594,RMVar_hsa_circ_72594,RMVar_hsa_circ_40819,RMVar_hsa_circ_370688,RMVar_hsa_circ_68694,RMVar_hsa_circ_217681,RMVar_hsa_circ_338642,RMVar_hsa_circ_85311,RMVar_hsa_circ_38017,RMVar_hsa_circ_92950,RMVar_hsa_circ_217687,RMVar_hsa_circ_217698,RMVar_hsa_circ_347090,RMVar_hsa_circ_319724,RMVar_hsa_circ_81356,RMVar_hsa_circ_217720,RMVar_hsa_circ_217699,RMVar_hsa_circ_217700,RMVar_hsa_circ_357551,RMVar_hsa_circ_118481,RMVar_hsa_circ_217708,RMVar_hsa_circ_217707,RMVar_hsa_circ_366507,RMVar_hsa_circ_53009,RMVar_hsa_circ_65535,RMVar_hsa_circ_217717,RMVar_hsa_circ_338301,RMVar_hsa_circ_376891,RMVar_hsa_circ_269345,RMVar_hsa_circ_365424,RMVar_hsa_circ_56523,RMVar_hsa_circ_369594,RMVar_hsa_circ_339305,RMVar_hsa_circ_319610,RMVar_hsa_circ_322359,RMVar_hsa_circ_217721,RMVar_hsa_circ_112692,RMVar_hsa_circ_285271,RMVar_hsa_circ_217719,RMVar_hsa_circ_318645,RMVar_hsa_circ_293732,RMVar_hsa_circ_284010,RMVar_hsa_circ_217727,RMVar_hsa_circ_217735,RMVar_hsa_circ_217725,RMVar_hsa_circ_217726,RMVar_hsa_circ_285186,RMVar_hsa_circ_307690,RMVar_hsa_circ_69873,RMVar_hsa_circ_299391,RMVar_hsa_circ_306145,RMVar_hsa_circ_361583,RMVar_hsa_circ_299759,RMVar_hsa_circ_279029,RMVar_hsa_circ_217742,RMVar_hsa_circ_122716,RMVar_hsa_circ_322115,RMVar_hsa_circ_217737,RMVar_hsa_circ_217739,RMVar_hsa_circ_217740,RMVar_hsa_circ_217738,RMVar_hsa_circ_217736,RMVar_hsa_circ_369776,RMVar_hsa_circ_276995,RMVar_hsa_circ_277214,RMVar_hsa_circ_273166,RMVar_hsa_circ_217746,RMVar_hsa_circ_217748,RMVar_hsa_circ_217747,RMVar_hsa_circ_217744,RMVar_hsa_circ_217745,RMVar_hsa_circ_217743,RMVar_hsa_circ_217741 29208 RMVar_ID_29208 Human_SNP_ID_132066534 A-to-I Human chr3 - 47723557 47723557 47723557 CTGCCGCCTTGACCTCCCAAAGTGCTGGGGTTACAGGTGTGAGCCACTGTGCCTGGCCTCCTTTT CTGCCGCCTTGACCTCCCAAAGTGCTGGGGTTTCAGGTGTGAGCCACTGTGCCTGGCCTCCTTTT T A SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1022276941 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19280,RMVar_hsa_circ_92479,RMVar_hsa_circ_217639,RMVar_hsa_circ_95274,RMVar_hsa_circ_372290,RMVar_hsa_circ_217644,RMVar_hsa_circ_217643,RMVar_hsa_circ_217662,RMVar_hsa_circ_87594,RMVar_hsa_circ_72594,RMVar_hsa_circ_40819,RMVar_hsa_circ_370688,RMVar_hsa_circ_68694,RMVar_hsa_circ_217681,RMVar_hsa_circ_338642,RMVar_hsa_circ_85311,RMVar_hsa_circ_38017,RMVar_hsa_circ_92950,RMVar_hsa_circ_217687,RMVar_hsa_circ_217698,RMVar_hsa_circ_347090,RMVar_hsa_circ_319724,RMVar_hsa_circ_81356,RMVar_hsa_circ_217720,RMVar_hsa_circ_217699,RMVar_hsa_circ_217700,RMVar_hsa_circ_357551,RMVar_hsa_circ_118481,RMVar_hsa_circ_217708,RMVar_hsa_circ_217707,RMVar_hsa_circ_366507,RMVar_hsa_circ_53009,RMVar_hsa_circ_65535,RMVar_hsa_circ_217717,RMVar_hsa_circ_338301,RMVar_hsa_circ_376891,RMVar_hsa_circ_269345,RMVar_hsa_circ_365424,RMVar_hsa_circ_56523,RMVar_hsa_circ_369594,RMVar_hsa_circ_339305,RMVar_hsa_circ_319610,RMVar_hsa_circ_322359,RMVar_hsa_circ_217721,RMVar_hsa_circ_112692,RMVar_hsa_circ_285271,RMVar_hsa_circ_217719,RMVar_hsa_circ_318645,RMVar_hsa_circ_293732,RMVar_hsa_circ_284010,RMVar_hsa_circ_217727,RMVar_hsa_circ_217735,RMVar_hsa_circ_217725,RMVar_hsa_circ_217726,RMVar_hsa_circ_285186,RMVar_hsa_circ_307690,RMVar_hsa_circ_69873,RMVar_hsa_circ_299391,RMVar_hsa_circ_306145,RMVar_hsa_circ_361583,RMVar_hsa_circ_299759,RMVar_hsa_circ_279029,RMVar_hsa_circ_217742,RMVar_hsa_circ_122716,RMVar_hsa_circ_322115,RMVar_hsa_circ_217737,RMVar_hsa_circ_217739,RMVar_hsa_circ_217740,RMVar_hsa_circ_217738,RMVar_hsa_circ_217736,RMVar_hsa_circ_369776,RMVar_hsa_circ_276995,RMVar_hsa_circ_277214,RMVar_hsa_circ_273166,RMVar_hsa_circ_217746,RMVar_hsa_circ_217748,RMVar_hsa_circ_217747,RMVar_hsa_circ_217744,RMVar_hsa_circ_217745,RMVar_hsa_circ_217743,RMVar_hsa_circ_217741 29209 RMVar_ID_29209 Human_SNP_ID_132066535 A-to-I Human chr3 - 47723557 47723557 47723557 CTGCCGCCTTGACCTCCCAAAGTGCTGGGGTTACAGGTGTGAGCCACTGTGCCTGGCCTCCTTTT CTGCCGCCTTGACCTCCCAAAGTGCTGGGGTTGCAGGTGTGAGCCACTGTGCCTGGCCTCCTTTT T C SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1022276941 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19280,RMVar_hsa_circ_92479,RMVar_hsa_circ_217639,RMVar_hsa_circ_95274,RMVar_hsa_circ_372290,RMVar_hsa_circ_217644,RMVar_hsa_circ_217643,RMVar_hsa_circ_217662,RMVar_hsa_circ_87594,RMVar_hsa_circ_72594,RMVar_hsa_circ_40819,RMVar_hsa_circ_370688,RMVar_hsa_circ_68694,RMVar_hsa_circ_217681,RMVar_hsa_circ_338642,RMVar_hsa_circ_85311,RMVar_hsa_circ_38017,RMVar_hsa_circ_92950,RMVar_hsa_circ_217687,RMVar_hsa_circ_217698,RMVar_hsa_circ_347090,RMVar_hsa_circ_319724,RMVar_hsa_circ_81356,RMVar_hsa_circ_217720,RMVar_hsa_circ_217699,RMVar_hsa_circ_217700,RMVar_hsa_circ_357551,RMVar_hsa_circ_118481,RMVar_hsa_circ_217708,RMVar_hsa_circ_217707,RMVar_hsa_circ_366507,RMVar_hsa_circ_53009,RMVar_hsa_circ_65535,RMVar_hsa_circ_217717,RMVar_hsa_circ_338301,RMVar_hsa_circ_376891,RMVar_hsa_circ_269345,RMVar_hsa_circ_365424,RMVar_hsa_circ_56523,RMVar_hsa_circ_369594,RMVar_hsa_circ_339305,RMVar_hsa_circ_319610,RMVar_hsa_circ_322359,RMVar_hsa_circ_217721,RMVar_hsa_circ_112692,RMVar_hsa_circ_285271,RMVar_hsa_circ_217719,RMVar_hsa_circ_318645,RMVar_hsa_circ_293732,RMVar_hsa_circ_284010,RMVar_hsa_circ_217727,RMVar_hsa_circ_217735,RMVar_hsa_circ_217725,RMVar_hsa_circ_217726,RMVar_hsa_circ_285186,RMVar_hsa_circ_307690,RMVar_hsa_circ_69873,RMVar_hsa_circ_299391,RMVar_hsa_circ_306145,RMVar_hsa_circ_361583,RMVar_hsa_circ_299759,RMVar_hsa_circ_279029,RMVar_hsa_circ_217742,RMVar_hsa_circ_122716,RMVar_hsa_circ_322115,RMVar_hsa_circ_217737,RMVar_hsa_circ_217739,RMVar_hsa_circ_217740,RMVar_hsa_circ_217738,RMVar_hsa_circ_217736,RMVar_hsa_circ_369776,RMVar_hsa_circ_276995,RMVar_hsa_circ_277214,RMVar_hsa_circ_273166,RMVar_hsa_circ_217746,RMVar_hsa_circ_217748,RMVar_hsa_circ_217747,RMVar_hsa_circ_217744,RMVar_hsa_circ_217745,RMVar_hsa_circ_217743,RMVar_hsa_circ_217741 29210 RMVar_ID_29210 Human_SNP_ID_132066999 A-to-I Human chr3 - 47725543 47725543 47725543 GGGAGGCTGAGGTGGGAGAATTGCTCAAACCCAGGAGGCGGAGGTTGCGGTGAGCCAAGATGGCA GGGAGGCTGAGGTGGGAGAATTGCTCAAACCCGGGAGGCGGAGGTTGCGGTGAGCCAAGATGGCA T C SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs571391659 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14849813,Human_RBP_ID_17573596,Human_RBP_ID_25739697 RMVar_hsa_circ_19280,RMVar_hsa_circ_92479,RMVar_hsa_circ_217639,RMVar_hsa_circ_95274,RMVar_hsa_circ_372290,RMVar_hsa_circ_217644,RMVar_hsa_circ_217643,RMVar_hsa_circ_217662,RMVar_hsa_circ_87594,RMVar_hsa_circ_72594,RMVar_hsa_circ_40819,RMVar_hsa_circ_370688,RMVar_hsa_circ_68694,RMVar_hsa_circ_217681,RMVar_hsa_circ_338642,RMVar_hsa_circ_85311,RMVar_hsa_circ_38017,RMVar_hsa_circ_92950,RMVar_hsa_circ_217687,RMVar_hsa_circ_217698,RMVar_hsa_circ_347090,RMVar_hsa_circ_319724,RMVar_hsa_circ_81356,RMVar_hsa_circ_217720,RMVar_hsa_circ_217699,RMVar_hsa_circ_217700,RMVar_hsa_circ_357551,RMVar_hsa_circ_118481,RMVar_hsa_circ_217708,RMVar_hsa_circ_217707,RMVar_hsa_circ_366507,RMVar_hsa_circ_53009,RMVar_hsa_circ_65535,RMVar_hsa_circ_217717,RMVar_hsa_circ_338301,RMVar_hsa_circ_376891,RMVar_hsa_circ_269345,RMVar_hsa_circ_365424,RMVar_hsa_circ_56523,RMVar_hsa_circ_369594,RMVar_hsa_circ_339305,RMVar_hsa_circ_319610,RMVar_hsa_circ_322359,RMVar_hsa_circ_217721,RMVar_hsa_circ_112692,RMVar_hsa_circ_285271,RMVar_hsa_circ_217719,RMVar_hsa_circ_318645,RMVar_hsa_circ_293732,RMVar_hsa_circ_284010,RMVar_hsa_circ_217727,RMVar_hsa_circ_217735,RMVar_hsa_circ_217725,RMVar_hsa_circ_217726,RMVar_hsa_circ_285186,RMVar_hsa_circ_307690,RMVar_hsa_circ_69873,RMVar_hsa_circ_299391,RMVar_hsa_circ_306145,RMVar_hsa_circ_361583,RMVar_hsa_circ_299759,RMVar_hsa_circ_279029,RMVar_hsa_circ_217742,RMVar_hsa_circ_122716,RMVar_hsa_circ_322115,RMVar_hsa_circ_217737,RMVar_hsa_circ_217739,RMVar_hsa_circ_217740,RMVar_hsa_circ_217738,RMVar_hsa_circ_217736,RMVar_hsa_circ_369776,RMVar_hsa_circ_276995,RMVar_hsa_circ_277214,RMVar_hsa_circ_273166,RMVar_hsa_circ_217746,RMVar_hsa_circ_217748,RMVar_hsa_circ_217747,RMVar_hsa_circ_217744,RMVar_hsa_circ_217745,RMVar_hsa_circ_217743,RMVar_hsa_circ_217741 29211 RMVar_ID_29211 Human_SNP_ID_132067052 A-to-I Human chr3 - 47725727 47725727 47725727 CACAGTTGGGCTGGGCCCGATGGCTCATGCCTATAATCCCAGCACTTTGGGATGCTGAGGCAGGC CACAGTTGGGCTGGGCCCGATGGCTCATGCCTGTAATCCCAGCACTTTGGGATGCTGAGGCAGGC T C SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1406158520 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19280,RMVar_hsa_circ_92479,RMVar_hsa_circ_217639,RMVar_hsa_circ_95274,RMVar_hsa_circ_372290,RMVar_hsa_circ_217644,RMVar_hsa_circ_217643,RMVar_hsa_circ_217662,RMVar_hsa_circ_87594,RMVar_hsa_circ_72594,RMVar_hsa_circ_40819,RMVar_hsa_circ_370688,RMVar_hsa_circ_68694,RMVar_hsa_circ_217681,RMVar_hsa_circ_338642,RMVar_hsa_circ_85311,RMVar_hsa_circ_38017,RMVar_hsa_circ_92950,RMVar_hsa_circ_217687,RMVar_hsa_circ_217698,RMVar_hsa_circ_347090,RMVar_hsa_circ_319724,RMVar_hsa_circ_81356,RMVar_hsa_circ_217720,RMVar_hsa_circ_217699,RMVar_hsa_circ_217700,RMVar_hsa_circ_357551,RMVar_hsa_circ_118481,RMVar_hsa_circ_217708,RMVar_hsa_circ_217707,RMVar_hsa_circ_366507,RMVar_hsa_circ_53009,RMVar_hsa_circ_65535,RMVar_hsa_circ_217717,RMVar_hsa_circ_338301,RMVar_hsa_circ_376891,RMVar_hsa_circ_269345,RMVar_hsa_circ_365424,RMVar_hsa_circ_56523,RMVar_hsa_circ_369594,RMVar_hsa_circ_339305,RMVar_hsa_circ_319610,RMVar_hsa_circ_322359,RMVar_hsa_circ_217721,RMVar_hsa_circ_112692,RMVar_hsa_circ_285271,RMVar_hsa_circ_217719,RMVar_hsa_circ_318645,RMVar_hsa_circ_293732,RMVar_hsa_circ_284010,RMVar_hsa_circ_217727,RMVar_hsa_circ_217735,RMVar_hsa_circ_217725,RMVar_hsa_circ_217726,RMVar_hsa_circ_285186,RMVar_hsa_circ_307690,RMVar_hsa_circ_69873,RMVar_hsa_circ_299391,RMVar_hsa_circ_306145,RMVar_hsa_circ_361583,RMVar_hsa_circ_299759,RMVar_hsa_circ_279029,RMVar_hsa_circ_217742,RMVar_hsa_circ_122716,RMVar_hsa_circ_322115,RMVar_hsa_circ_217737,RMVar_hsa_circ_217739,RMVar_hsa_circ_217740,RMVar_hsa_circ_217738,RMVar_hsa_circ_217736,RMVar_hsa_circ_369776,RMVar_hsa_circ_276995,RMVar_hsa_circ_277214,RMVar_hsa_circ_273166,RMVar_hsa_circ_217746,RMVar_hsa_circ_217748,RMVar_hsa_circ_217747,RMVar_hsa_circ_217744,RMVar_hsa_circ_217745,RMVar_hsa_circ_217743,RMVar_hsa_circ_217741 29212 RMVar_ID_29212 Human_SNP_ID_132067104 A-to-I Human chr3 - 47725914 47725914 47725914 GGGATTACAGGCATCCACCACGACACCCAGCTAATGTTTGTATTTTTAGTAGAGACGGGGTTTCA GGGATTACAGGCATCCACCACGACACCCAGCTGATGTTTGTATTTTTAGTAGAGACGGGGTTTCA T C SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1352011119 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19280,RMVar_hsa_circ_92479,RMVar_hsa_circ_217639,RMVar_hsa_circ_95274,RMVar_hsa_circ_372290,RMVar_hsa_circ_217644,RMVar_hsa_circ_217643,RMVar_hsa_circ_217662,RMVar_hsa_circ_87594,RMVar_hsa_circ_72594,RMVar_hsa_circ_40819,RMVar_hsa_circ_370688,RMVar_hsa_circ_68694,RMVar_hsa_circ_217681,RMVar_hsa_circ_338642,RMVar_hsa_circ_85311,RMVar_hsa_circ_38017,RMVar_hsa_circ_92950,RMVar_hsa_circ_217687,RMVar_hsa_circ_217698,RMVar_hsa_circ_347090,RMVar_hsa_circ_319724,RMVar_hsa_circ_81356,RMVar_hsa_circ_217720,RMVar_hsa_circ_217699,RMVar_hsa_circ_217700,RMVar_hsa_circ_357551,RMVar_hsa_circ_118481,RMVar_hsa_circ_217708,RMVar_hsa_circ_217707,RMVar_hsa_circ_366507,RMVar_hsa_circ_53009,RMVar_hsa_circ_65535,RMVar_hsa_circ_217717,RMVar_hsa_circ_338301,RMVar_hsa_circ_376891,RMVar_hsa_circ_269345,RMVar_hsa_circ_365424,RMVar_hsa_circ_56523,RMVar_hsa_circ_369594,RMVar_hsa_circ_339305,RMVar_hsa_circ_319610,RMVar_hsa_circ_322359,RMVar_hsa_circ_217721,RMVar_hsa_circ_112692,RMVar_hsa_circ_285271,RMVar_hsa_circ_217719,RMVar_hsa_circ_318645,RMVar_hsa_circ_293732,RMVar_hsa_circ_284010,RMVar_hsa_circ_217727,RMVar_hsa_circ_217735,RMVar_hsa_circ_217725,RMVar_hsa_circ_217726,RMVar_hsa_circ_285186,RMVar_hsa_circ_307690,RMVar_hsa_circ_69873,RMVar_hsa_circ_299391,RMVar_hsa_circ_306145,RMVar_hsa_circ_361583,RMVar_hsa_circ_299759,RMVar_hsa_circ_279029,RMVar_hsa_circ_217742,RMVar_hsa_circ_122716,RMVar_hsa_circ_322115,RMVar_hsa_circ_217737,RMVar_hsa_circ_217739,RMVar_hsa_circ_217740,RMVar_hsa_circ_217738,RMVar_hsa_circ_217736,RMVar_hsa_circ_369776,RMVar_hsa_circ_276995,RMVar_hsa_circ_277214,RMVar_hsa_circ_273166,RMVar_hsa_circ_217746,RMVar_hsa_circ_217748,RMVar_hsa_circ_217747,RMVar_hsa_circ_217744,RMVar_hsa_circ_217745,RMVar_hsa_circ_217743,RMVar_hsa_circ_217741 29213 RMVar_ID_29213 Human_SNP_ID_132067116 A-to-I Human chr3 - 47725980 47725980 47725980 TTGGCTCACTGCAGCTTCCGCCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGC TTGGCTCACTGCAGCTTCCGCCTCCCAGGTTCCAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGC T G SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs575332233 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19280,RMVar_hsa_circ_92479,RMVar_hsa_circ_217639,RMVar_hsa_circ_95274,RMVar_hsa_circ_372290,RMVar_hsa_circ_217644,RMVar_hsa_circ_217643,RMVar_hsa_circ_217662,RMVar_hsa_circ_87594,RMVar_hsa_circ_72594,RMVar_hsa_circ_40819,RMVar_hsa_circ_370688,RMVar_hsa_circ_68694,RMVar_hsa_circ_217681,RMVar_hsa_circ_338642,RMVar_hsa_circ_85311,RMVar_hsa_circ_38017,RMVar_hsa_circ_92950,RMVar_hsa_circ_217687,RMVar_hsa_circ_217698,RMVar_hsa_circ_347090,RMVar_hsa_circ_319724,RMVar_hsa_circ_81356,RMVar_hsa_circ_217720,RMVar_hsa_circ_217699,RMVar_hsa_circ_217700,RMVar_hsa_circ_357551,RMVar_hsa_circ_118481,RMVar_hsa_circ_217708,RMVar_hsa_circ_217707,RMVar_hsa_circ_366507,RMVar_hsa_circ_53009,RMVar_hsa_circ_65535,RMVar_hsa_circ_217717,RMVar_hsa_circ_338301,RMVar_hsa_circ_376891,RMVar_hsa_circ_269345,RMVar_hsa_circ_365424,RMVar_hsa_circ_56523,RMVar_hsa_circ_369594,RMVar_hsa_circ_339305,RMVar_hsa_circ_319610,RMVar_hsa_circ_322359,RMVar_hsa_circ_217721,RMVar_hsa_circ_112692,RMVar_hsa_circ_285271,RMVar_hsa_circ_217719,RMVar_hsa_circ_318645,RMVar_hsa_circ_293732,RMVar_hsa_circ_284010,RMVar_hsa_circ_217727,RMVar_hsa_circ_217735,RMVar_hsa_circ_217725,RMVar_hsa_circ_217726,RMVar_hsa_circ_285186,RMVar_hsa_circ_307690,RMVar_hsa_circ_69873,RMVar_hsa_circ_299391,RMVar_hsa_circ_306145,RMVar_hsa_circ_361583,RMVar_hsa_circ_299759,RMVar_hsa_circ_279029,RMVar_hsa_circ_217742,RMVar_hsa_circ_122716,RMVar_hsa_circ_322115,RMVar_hsa_circ_217737,RMVar_hsa_circ_217739,RMVar_hsa_circ_217740,RMVar_hsa_circ_217738,RMVar_hsa_circ_217736,RMVar_hsa_circ_369776,RMVar_hsa_circ_276995,RMVar_hsa_circ_277214,RMVar_hsa_circ_273166,RMVar_hsa_circ_217746,RMVar_hsa_circ_217748,RMVar_hsa_circ_217747,RMVar_hsa_circ_217744,RMVar_hsa_circ_217745,RMVar_hsa_circ_217743,RMVar_hsa_circ_217741 29214 RMVar_ID_29214 Human_SNP_ID_132067375 A-to-I Human chr3 - 47726975 47726975 47726975 AAACTCCTGACCTCAAGTGATCCAAACGCCTCAGCCTCCCAAAGTGCTGGTATTAGAGGCGTGAG AAACTCCTGACCTCAAGTGATCCAAACGCCTCGGCCTCCCAAAGTGCTGGTATTAGAGGCGTGAG T C SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1488895636 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7201765 RMVar_hsa_circ_19280,RMVar_hsa_circ_92479,RMVar_hsa_circ_217639,RMVar_hsa_circ_95274,RMVar_hsa_circ_372290,RMVar_hsa_circ_217644,RMVar_hsa_circ_217643,RMVar_hsa_circ_217662,RMVar_hsa_circ_87594,RMVar_hsa_circ_72594,RMVar_hsa_circ_40819,RMVar_hsa_circ_370688,RMVar_hsa_circ_68694,RMVar_hsa_circ_217681,RMVar_hsa_circ_338642,RMVar_hsa_circ_85311,RMVar_hsa_circ_38017,RMVar_hsa_circ_92950,RMVar_hsa_circ_217687,RMVar_hsa_circ_217698,RMVar_hsa_circ_347090,RMVar_hsa_circ_319724,RMVar_hsa_circ_81356,RMVar_hsa_circ_217720,RMVar_hsa_circ_217699,RMVar_hsa_circ_217700,RMVar_hsa_circ_357551,RMVar_hsa_circ_118481,RMVar_hsa_circ_217708,RMVar_hsa_circ_217707,RMVar_hsa_circ_366507,RMVar_hsa_circ_53009,RMVar_hsa_circ_65535,RMVar_hsa_circ_217717,RMVar_hsa_circ_338301,RMVar_hsa_circ_376891,RMVar_hsa_circ_269345,RMVar_hsa_circ_365424,RMVar_hsa_circ_56523,RMVar_hsa_circ_369594,RMVar_hsa_circ_339305,RMVar_hsa_circ_319610,RMVar_hsa_circ_322359,RMVar_hsa_circ_217721,RMVar_hsa_circ_112692,RMVar_hsa_circ_285271,RMVar_hsa_circ_217719,RMVar_hsa_circ_318645,RMVar_hsa_circ_293732,RMVar_hsa_circ_284010,RMVar_hsa_circ_217727,RMVar_hsa_circ_217735,RMVar_hsa_circ_217725,RMVar_hsa_circ_217726,RMVar_hsa_circ_285186,RMVar_hsa_circ_307690,RMVar_hsa_circ_69873,RMVar_hsa_circ_299391,RMVar_hsa_circ_306145,RMVar_hsa_circ_361583,RMVar_hsa_circ_299759,RMVar_hsa_circ_279029,RMVar_hsa_circ_217742,RMVar_hsa_circ_122716,RMVar_hsa_circ_322115,RMVar_hsa_circ_217737,RMVar_hsa_circ_217739,RMVar_hsa_circ_217740,RMVar_hsa_circ_217738,RMVar_hsa_circ_217736,RMVar_hsa_circ_369776,RMVar_hsa_circ_276995,RMVar_hsa_circ_277214,RMVar_hsa_circ_273166,RMVar_hsa_circ_217746,RMVar_hsa_circ_217748,RMVar_hsa_circ_217747,RMVar_hsa_circ_217744,RMVar_hsa_circ_217745,RMVar_hsa_circ_217743,RMVar_hsa_circ_217741 29215 RMVar_ID_29215 Human_SNP_ID_132067772 A-to-I Human chr3 - 47728184 47728184 47728184 TACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAACCTGGGATATGGAGGTTGCAGTGAGTCAAGA TACTTGGGAGGCTGAGGCAGGAGAATCGCTTGCACCTGGGATATGGAGGTTGCAGTGAGTCAAGA T G SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs532766194 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22605759 RMVar_hsa_circ_19280,RMVar_hsa_circ_92479,RMVar_hsa_circ_217639,RMVar_hsa_circ_95274,RMVar_hsa_circ_372290,RMVar_hsa_circ_217644,RMVar_hsa_circ_217643,RMVar_hsa_circ_217662,RMVar_hsa_circ_87594,RMVar_hsa_circ_72594,RMVar_hsa_circ_40819,RMVar_hsa_circ_370688,RMVar_hsa_circ_68694,RMVar_hsa_circ_217681,RMVar_hsa_circ_338642,RMVar_hsa_circ_85311,RMVar_hsa_circ_38017,RMVar_hsa_circ_92950,RMVar_hsa_circ_217687,RMVar_hsa_circ_217698,RMVar_hsa_circ_347090,RMVar_hsa_circ_319724,RMVar_hsa_circ_81356,RMVar_hsa_circ_217720,RMVar_hsa_circ_217699,RMVar_hsa_circ_217700,RMVar_hsa_circ_357551,RMVar_hsa_circ_118481,RMVar_hsa_circ_217708,RMVar_hsa_circ_217707,RMVar_hsa_circ_366507,RMVar_hsa_circ_53009,RMVar_hsa_circ_65535,RMVar_hsa_circ_217717,RMVar_hsa_circ_338301,RMVar_hsa_circ_376891,RMVar_hsa_circ_269345,RMVar_hsa_circ_365424,RMVar_hsa_circ_56523,RMVar_hsa_circ_369594,RMVar_hsa_circ_339305,RMVar_hsa_circ_319610,RMVar_hsa_circ_322359,RMVar_hsa_circ_217721,RMVar_hsa_circ_112692,RMVar_hsa_circ_285271,RMVar_hsa_circ_217719,RMVar_hsa_circ_318645,RMVar_hsa_circ_293732,RMVar_hsa_circ_284010,RMVar_hsa_circ_217727,RMVar_hsa_circ_217735,RMVar_hsa_circ_217725,RMVar_hsa_circ_217726,RMVar_hsa_circ_285186,RMVar_hsa_circ_307690,RMVar_hsa_circ_69873,RMVar_hsa_circ_299391,RMVar_hsa_circ_306145,RMVar_hsa_circ_361583,RMVar_hsa_circ_299759,RMVar_hsa_circ_279029,RMVar_hsa_circ_217742,RMVar_hsa_circ_122716,RMVar_hsa_circ_322115,RMVar_hsa_circ_217737,RMVar_hsa_circ_217739,RMVar_hsa_circ_217740,RMVar_hsa_circ_217738,RMVar_hsa_circ_217736,RMVar_hsa_circ_369776,RMVar_hsa_circ_276995,RMVar_hsa_circ_277214,RMVar_hsa_circ_273166,RMVar_hsa_circ_217746,RMVar_hsa_circ_217748,RMVar_hsa_circ_217747,RMVar_hsa_circ_217744,RMVar_hsa_circ_217745,RMVar_hsa_circ_217743,RMVar_hsa_circ_217741 29216 RMVar_ID_29216 Human_SNP_ID_132067809 A-to-I Human chr3 - 47728352 47728352 47728352 TGGACCTGGTGTCTCACGCCTGTAATCCCAGCAGTTTGGGAGTCCGAGGTGGGTGGATCACTTGA TGGACCTGGTGTCTCACGCCTGTAATCCCAGCCGTTTGGGAGTCCGAGGTGGGTGGATCACTTGA T G SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1395106442 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14849847 RMVar_hsa_circ_19280,RMVar_hsa_circ_92479,RMVar_hsa_circ_217639,RMVar_hsa_circ_95274,RMVar_hsa_circ_372290,RMVar_hsa_circ_217644,RMVar_hsa_circ_217643,RMVar_hsa_circ_217662,RMVar_hsa_circ_87594,RMVar_hsa_circ_72594,RMVar_hsa_circ_40819,RMVar_hsa_circ_370688,RMVar_hsa_circ_68694,RMVar_hsa_circ_217681,RMVar_hsa_circ_338642,RMVar_hsa_circ_85311,RMVar_hsa_circ_38017,RMVar_hsa_circ_92950,RMVar_hsa_circ_217687,RMVar_hsa_circ_217698,RMVar_hsa_circ_347090,RMVar_hsa_circ_319724,RMVar_hsa_circ_81356,RMVar_hsa_circ_217720,RMVar_hsa_circ_217699,RMVar_hsa_circ_217700,RMVar_hsa_circ_357551,RMVar_hsa_circ_118481,RMVar_hsa_circ_217708,RMVar_hsa_circ_217707,RMVar_hsa_circ_366507,RMVar_hsa_circ_53009,RMVar_hsa_circ_65535,RMVar_hsa_circ_217717,RMVar_hsa_circ_338301,RMVar_hsa_circ_376891,RMVar_hsa_circ_269345,RMVar_hsa_circ_365424,RMVar_hsa_circ_56523,RMVar_hsa_circ_369594,RMVar_hsa_circ_339305,RMVar_hsa_circ_319610,RMVar_hsa_circ_322359,RMVar_hsa_circ_217721,RMVar_hsa_circ_112692,RMVar_hsa_circ_285271,RMVar_hsa_circ_217719,RMVar_hsa_circ_318645,RMVar_hsa_circ_293732,RMVar_hsa_circ_284010,RMVar_hsa_circ_217727,RMVar_hsa_circ_217735,RMVar_hsa_circ_217725,RMVar_hsa_circ_217726,RMVar_hsa_circ_285186,RMVar_hsa_circ_307690,RMVar_hsa_circ_69873,RMVar_hsa_circ_299391,RMVar_hsa_circ_306145,RMVar_hsa_circ_361583,RMVar_hsa_circ_299759,RMVar_hsa_circ_279029,RMVar_hsa_circ_217742,RMVar_hsa_circ_122716,RMVar_hsa_circ_322115,RMVar_hsa_circ_217737,RMVar_hsa_circ_217739,RMVar_hsa_circ_217740,RMVar_hsa_circ_217738,RMVar_hsa_circ_217736,RMVar_hsa_circ_369776,RMVar_hsa_circ_276995,RMVar_hsa_circ_277214,RMVar_hsa_circ_273166,RMVar_hsa_circ_217746,RMVar_hsa_circ_217748,RMVar_hsa_circ_217747,RMVar_hsa_circ_217744,RMVar_hsa_circ_217745,RMVar_hsa_circ_217743,RMVar_hsa_circ_217741 29217 RMVar_ID_29217 Human_SNP_ID_132068167 A-to-I Human chr3 - 47729665 47729665 47729665 GTAATAGTACCTGACTGAACACAGTGGCTCACATCTTTAATCCCAGAACTTTGGAAGGCCAAGGC GTAATAGTACCTGACTGAACACAGTGGCTCACGTCTTTAATCCCAGAACTTTGGAAGGCCAAGGC T C SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs983020961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14849880 RMVar_hsa_circ_19280,RMVar_hsa_circ_92479,RMVar_hsa_circ_217639,RMVar_hsa_circ_95274,RMVar_hsa_circ_372290,RMVar_hsa_circ_217644,RMVar_hsa_circ_217643,RMVar_hsa_circ_217662,RMVar_hsa_circ_87594,RMVar_hsa_circ_72594,RMVar_hsa_circ_40819,RMVar_hsa_circ_370688,RMVar_hsa_circ_68694,RMVar_hsa_circ_217681,RMVar_hsa_circ_85311,RMVar_hsa_circ_38017,RMVar_hsa_circ_217687,RMVar_hsa_circ_319724,RMVar_hsa_circ_81356,RMVar_hsa_circ_217720,RMVar_hsa_circ_217699,RMVar_hsa_circ_357551,RMVar_hsa_circ_118481,RMVar_hsa_circ_217708,RMVar_hsa_circ_217707,RMVar_hsa_circ_366507,RMVar_hsa_circ_65535,RMVar_hsa_circ_217717,RMVar_hsa_circ_338301,RMVar_hsa_circ_376891,RMVar_hsa_circ_269345,RMVar_hsa_circ_365424,RMVar_hsa_circ_56523,RMVar_hsa_circ_369594,RMVar_hsa_circ_339305,RMVar_hsa_circ_319610,RMVar_hsa_circ_112692,RMVar_hsa_circ_217719,RMVar_hsa_circ_318645,RMVar_hsa_circ_293732,RMVar_hsa_circ_284010,RMVar_hsa_circ_217735,RMVar_hsa_circ_217725,RMVar_hsa_circ_217726,RMVar_hsa_circ_307690,RMVar_hsa_circ_69873,RMVar_hsa_circ_299391,RMVar_hsa_circ_306145,RMVar_hsa_circ_361583,RMVar_hsa_circ_279029,RMVar_hsa_circ_217742,RMVar_hsa_circ_122716,RMVar_hsa_circ_322115,RMVar_hsa_circ_217737,RMVar_hsa_circ_217739,RMVar_hsa_circ_217738,RMVar_hsa_circ_217736,RMVar_hsa_circ_369776,RMVar_hsa_circ_277214,RMVar_hsa_circ_273166,RMVar_hsa_circ_217746,RMVar_hsa_circ_217747,RMVar_hsa_circ_217744,RMVar_hsa_circ_217745,RMVar_hsa_circ_217743,RMVar_hsa_circ_217751,RMVar_hsa_circ_52647,RMVar_hsa_circ_281301,RMVar_hsa_circ_217741,RMVar_hsa_circ_296848,RMVar_hsa_circ_270855,RMVar_hsa_circ_217752,RMVar_hsa_circ_217753 29218 RMVar_ID_29218 Human_SNP_ID_132068261 A-to-I Human chr3 - 47730069 47730069 47730069 GCTCAAGTGATTCTTCTGCCTCAGCCTCTTGAATAGCTGAGATTACAGACGTGTGCCACCACGCC GCTCAAGTGATTCTTCTGCCTCAGCCTCTTGAGTAGCTGAGATTACAGACGTGTGCCACCACGCC T C SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1448280767 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19280,RMVar_hsa_circ_92479,RMVar_hsa_circ_217639,RMVar_hsa_circ_95274,RMVar_hsa_circ_372290,RMVar_hsa_circ_217644,RMVar_hsa_circ_217643,RMVar_hsa_circ_217662,RMVar_hsa_circ_87594,RMVar_hsa_circ_72594,RMVar_hsa_circ_40819,RMVar_hsa_circ_370688,RMVar_hsa_circ_68694,RMVar_hsa_circ_217681,RMVar_hsa_circ_85311,RMVar_hsa_circ_38017,RMVar_hsa_circ_217687,RMVar_hsa_circ_319724,RMVar_hsa_circ_81356,RMVar_hsa_circ_217720,RMVar_hsa_circ_217699,RMVar_hsa_circ_357551,RMVar_hsa_circ_118481,RMVar_hsa_circ_217708,RMVar_hsa_circ_217707,RMVar_hsa_circ_366507,RMVar_hsa_circ_65535,RMVar_hsa_circ_217717,RMVar_hsa_circ_338301,RMVar_hsa_circ_376891,RMVar_hsa_circ_269345,RMVar_hsa_circ_365424,RMVar_hsa_circ_56523,RMVar_hsa_circ_369594,RMVar_hsa_circ_339305,RMVar_hsa_circ_319610,RMVar_hsa_circ_112692,RMVar_hsa_circ_217719,RMVar_hsa_circ_318645,RMVar_hsa_circ_293732,RMVar_hsa_circ_284010,RMVar_hsa_circ_217735,RMVar_hsa_circ_217725,RMVar_hsa_circ_217726,RMVar_hsa_circ_307690,RMVar_hsa_circ_69873,RMVar_hsa_circ_299391,RMVar_hsa_circ_306145,RMVar_hsa_circ_361583,RMVar_hsa_circ_279029,RMVar_hsa_circ_217742,RMVar_hsa_circ_122716,RMVar_hsa_circ_322115,RMVar_hsa_circ_217737,RMVar_hsa_circ_217739,RMVar_hsa_circ_217738,RMVar_hsa_circ_217736,RMVar_hsa_circ_369776,RMVar_hsa_circ_277214,RMVar_hsa_circ_273166,RMVar_hsa_circ_217746,RMVar_hsa_circ_217747,RMVar_hsa_circ_217744,RMVar_hsa_circ_217745,RMVar_hsa_circ_217743,RMVar_hsa_circ_217751,RMVar_hsa_circ_52647,RMVar_hsa_circ_281301,RMVar_hsa_circ_217741,RMVar_hsa_circ_296848,RMVar_hsa_circ_270855,RMVar_hsa_circ_217752,RMVar_hsa_circ_217753 29219 RMVar_ID_29219 Human_SNP_ID_132071692 A-to-I Human chr3 - 47743731 47743731 47743731 TCGGCTCACTGCAACCTCTACCTCCCAGGTTCAAGCAGTTCTCCTGCCTCACCCTCCTGAGTAGC TCGGCTCACTGCAACCTCTACCTCCCAGGTTCGAGCAGTTCTCCTGCCTCACCCTCCTGAGTAGC T C SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1339562643 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92479,RMVar_hsa_circ_217639,RMVar_hsa_circ_372290,RMVar_hsa_circ_217643,RMVar_hsa_circ_217662,RMVar_hsa_circ_87594,RMVar_hsa_circ_72594,RMVar_hsa_circ_40819,RMVar_hsa_circ_370688,RMVar_hsa_circ_68694,RMVar_hsa_circ_217681,RMVar_hsa_circ_85311,RMVar_hsa_circ_217687,RMVar_hsa_circ_319724,RMVar_hsa_circ_81356,RMVar_hsa_circ_217699,RMVar_hsa_circ_357551,RMVar_hsa_circ_217707,RMVar_hsa_circ_366507,RMVar_hsa_circ_65535,RMVar_hsa_circ_338301,RMVar_hsa_circ_365424,RMVar_hsa_circ_339305,RMVar_hsa_circ_319610,RMVar_hsa_circ_112692,RMVar_hsa_circ_217719,RMVar_hsa_circ_293732,RMVar_hsa_circ_284010,RMVar_hsa_circ_217735,RMVar_hsa_circ_217725,RMVar_hsa_circ_307690,RMVar_hsa_circ_69873,RMVar_hsa_circ_306145,RMVar_hsa_circ_279029,RMVar_hsa_circ_217742,RMVar_hsa_circ_122716,RMVar_hsa_circ_322115,RMVar_hsa_circ_217737,RMVar_hsa_circ_217739,RMVar_hsa_circ_217738,RMVar_hsa_circ_217736,RMVar_hsa_circ_273166,RMVar_hsa_circ_217744,RMVar_hsa_circ_217745,RMVar_hsa_circ_217743,RMVar_hsa_circ_217741,RMVar_hsa_circ_296848,RMVar_hsa_circ_270855,RMVar_hsa_circ_217752,RMVar_hsa_circ_217753,RMVar_hsa_circ_217758,RMVar_hsa_circ_217757,RMVar_hsa_circ_287901,RMVar_hsa_circ_274650,RMVar_hsa_circ_217756,RMVar_hsa_circ_277586,RMVar_hsa_circ_285767,RMVar_hsa_circ_217759 29220 RMVar_ID_29220 Human_SNP_ID_132072120 A-to-I Human chr3 - 47745521 47745521 47745521 TTTAGTAGAAATAGGGTTTTGTCATGTTGGTCAGGCTGCTCTCAAACTCCTGGCCTCAAGCACTC TTTAGTAGAAATAGGGTTTTGTCATGTTGGTCGGGCTGCTCTCAAACTCCTGGCCTCAAGCACTC T C SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1315518977 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92479,RMVar_hsa_circ_217639,RMVar_hsa_circ_372290,RMVar_hsa_circ_217643,RMVar_hsa_circ_217662,RMVar_hsa_circ_87594,RMVar_hsa_circ_72594,RMVar_hsa_circ_40819,RMVar_hsa_circ_370688,RMVar_hsa_circ_68694,RMVar_hsa_circ_217681,RMVar_hsa_circ_85311,RMVar_hsa_circ_217687,RMVar_hsa_circ_319724,RMVar_hsa_circ_81356,RMVar_hsa_circ_217699,RMVar_hsa_circ_357551,RMVar_hsa_circ_217707,RMVar_hsa_circ_366507,RMVar_hsa_circ_65535,RMVar_hsa_circ_338301,RMVar_hsa_circ_365424,RMVar_hsa_circ_339305,RMVar_hsa_circ_319610,RMVar_hsa_circ_112692,RMVar_hsa_circ_217719,RMVar_hsa_circ_293732,RMVar_hsa_circ_284010,RMVar_hsa_circ_217735,RMVar_hsa_circ_217725,RMVar_hsa_circ_307690,RMVar_hsa_circ_69873,RMVar_hsa_circ_306145,RMVar_hsa_circ_279029,RMVar_hsa_circ_217742,RMVar_hsa_circ_122716,RMVar_hsa_circ_322115,RMVar_hsa_circ_217737,RMVar_hsa_circ_217739,RMVar_hsa_circ_217738,RMVar_hsa_circ_217736,RMVar_hsa_circ_273166,RMVar_hsa_circ_217744,RMVar_hsa_circ_217745,RMVar_hsa_circ_217743,RMVar_hsa_circ_217741,RMVar_hsa_circ_296848,RMVar_hsa_circ_270855,RMVar_hsa_circ_217752,RMVar_hsa_circ_217753,RMVar_hsa_circ_217758,RMVar_hsa_circ_217757,RMVar_hsa_circ_287901,RMVar_hsa_circ_274650,RMVar_hsa_circ_217756,RMVar_hsa_circ_277586,RMVar_hsa_circ_285767,RMVar_hsa_circ_217759 29221 RMVar_ID_29221 Human_SNP_ID_132072450 A-to-I Human chr3 - 47746828 47746828 47746828 TACTTAGGAGGCTGAGGCAGGAGAATCACTTGAACCTGGGAGGCGTAGGTTGCAGTGAGCCGAGA TACTTAGGAGGCTGAGGCAGGAGAATCACTTGGACCTGGGAGGCGTAGGTTGCAGTGAGCCGAGA T C SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs954602196 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92479,RMVar_hsa_circ_217639,RMVar_hsa_circ_372290,RMVar_hsa_circ_217643,RMVar_hsa_circ_217662,RMVar_hsa_circ_87594,RMVar_hsa_circ_72594,RMVar_hsa_circ_68694,RMVar_hsa_circ_81356,RMVar_hsa_circ_217699,RMVar_hsa_circ_357551,RMVar_hsa_circ_217707,RMVar_hsa_circ_366507,RMVar_hsa_circ_338301,RMVar_hsa_circ_365424,RMVar_hsa_circ_339305,RMVar_hsa_circ_293732,RMVar_hsa_circ_217735,RMVar_hsa_circ_307690,RMVar_hsa_circ_279029,RMVar_hsa_circ_217742,RMVar_hsa_circ_122716,RMVar_hsa_circ_322115,RMVar_hsa_circ_217737,RMVar_hsa_circ_217736,RMVar_hsa_circ_217741,RMVar_hsa_circ_270855,RMVar_hsa_circ_217753,RMVar_hsa_circ_217758,RMVar_hsa_circ_217757,RMVar_hsa_circ_287901,RMVar_hsa_circ_285767,RMVar_hsa_circ_217761,RMVar_hsa_circ_92310,RMVar_hsa_circ_285504,RMVar_hsa_circ_217760 29222 RMVar_ID_29222 Human_SNP_ID_132074807 A-to-I Human chr3 - 47755375 47755375 47755375 CTCCTGCCTCAGCCTCCCAAGTAGTTCGGACTACAGGCTGCCACCGTGCCTGTCTAATTTTTGTA CTCCTGCCTCAGCCTCCCAAGTAGTTCGGACTGCAGGCTGCCACCGTGCCTGTCTAATTTTTGTA T C SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1354168381 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14850475 RMVar_hsa_circ_92479,RMVar_hsa_circ_217639,RMVar_hsa_circ_372290,RMVar_hsa_circ_217643,RMVar_hsa_circ_217662,RMVar_hsa_circ_87594,RMVar_hsa_circ_72594,RMVar_hsa_circ_68694,RMVar_hsa_circ_81356,RMVar_hsa_circ_217699,RMVar_hsa_circ_357551,RMVar_hsa_circ_217707,RMVar_hsa_circ_366507,RMVar_hsa_circ_338301,RMVar_hsa_circ_365424,RMVar_hsa_circ_339305,RMVar_hsa_circ_293732,RMVar_hsa_circ_217735,RMVar_hsa_circ_307690,RMVar_hsa_circ_279029,RMVar_hsa_circ_217742,RMVar_hsa_circ_122716,RMVar_hsa_circ_322115,RMVar_hsa_circ_217737,RMVar_hsa_circ_217736,RMVar_hsa_circ_217741,RMVar_hsa_circ_270855,RMVar_hsa_circ_217753,RMVar_hsa_circ_217758,RMVar_hsa_circ_217757,RMVar_hsa_circ_287901,RMVar_hsa_circ_285767,RMVar_hsa_circ_217761,RMVar_hsa_circ_92310,RMVar_hsa_circ_285504,RMVar_hsa_circ_217760 29223 RMVar_ID_29223 Human_SNP_ID_132075157 A-to-I Human chr3 - 47756371 47756371 47756371 GCGCCACCATGCCTGGCTGGTTTTGTATTTTTAGTAGAGACGGGGTTTCTCCATGTTGGTCAGGC GCGCCACCATGCCTGGCTGGTTTTGTATTTTTGGTAGAGACGGGGTTTCTCCATGTTGGTCAGGC T C SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs989241800 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92479,RMVar_hsa_circ_217639,RMVar_hsa_circ_372290,RMVar_hsa_circ_217643,RMVar_hsa_circ_217662,RMVar_hsa_circ_87594,RMVar_hsa_circ_72594,RMVar_hsa_circ_68694,RMVar_hsa_circ_81356,RMVar_hsa_circ_217699,RMVar_hsa_circ_357551,RMVar_hsa_circ_217707,RMVar_hsa_circ_366507,RMVar_hsa_circ_338301,RMVar_hsa_circ_365424,RMVar_hsa_circ_339305,RMVar_hsa_circ_293732,RMVar_hsa_circ_217735,RMVar_hsa_circ_307690,RMVar_hsa_circ_279029,RMVar_hsa_circ_217742,RMVar_hsa_circ_122716,RMVar_hsa_circ_322115,RMVar_hsa_circ_217737,RMVar_hsa_circ_217736,RMVar_hsa_circ_217741,RMVar_hsa_circ_270855,RMVar_hsa_circ_217753,RMVar_hsa_circ_217758,RMVar_hsa_circ_217757,RMVar_hsa_circ_287901,RMVar_hsa_circ_285767,RMVar_hsa_circ_217761,RMVar_hsa_circ_92310,RMVar_hsa_circ_285504,RMVar_hsa_circ_217760 29224 RMVar_ID_29224 Human_SNP_ID_132076341 A-to-I Human chr3 - 47760623 47760623 47760623 GTCTTGCTCAGTTGCCCAGGCTGGAGTGCAGTAGCACAATCTTGGCTCACTGCAGTCTCCTCCCC GTCTTGCTCAGTTGCCCAGGCTGGAGTGCAGTGGCACAATCTTGGCTCACTGCAGTCTCCTCCCC T C SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1284298688 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92479,RMVar_hsa_circ_217639,RMVar_hsa_circ_372290,RMVar_hsa_circ_217643,RMVar_hsa_circ_217662,RMVar_hsa_circ_87594,RMVar_hsa_circ_72594,RMVar_hsa_circ_68694,RMVar_hsa_circ_81356,RMVar_hsa_circ_217699,RMVar_hsa_circ_357551,RMVar_hsa_circ_217707,RMVar_hsa_circ_366507,RMVar_hsa_circ_338301,RMVar_hsa_circ_365424,RMVar_hsa_circ_339305,RMVar_hsa_circ_293732,RMVar_hsa_circ_217735,RMVar_hsa_circ_307690,RMVar_hsa_circ_279029,RMVar_hsa_circ_217742,RMVar_hsa_circ_122716,RMVar_hsa_circ_322115,RMVar_hsa_circ_217737,RMVar_hsa_circ_217736,RMVar_hsa_circ_217741,RMVar_hsa_circ_270855,RMVar_hsa_circ_217753,RMVar_hsa_circ_217758,RMVar_hsa_circ_217757,RMVar_hsa_circ_287901,RMVar_hsa_circ_285767,RMVar_hsa_circ_217761,RMVar_hsa_circ_92310,RMVar_hsa_circ_285504,RMVar_hsa_circ_217760 29225 RMVar_ID_29225 Human_SNP_ID_132076991 A-to-I Human chr3 - 47763278 47763278 47763278 GCTGGGTGTGGTGGCTCATGCCTGTAATCCTAACGTTTTGGGAGGCTGAGGCAGGAGGATCACTT GCTGGGTGTGGTGGCTCATGCCTGTAATCCTATCGTTTTGGGAGGCTGAGGCAGGAGGATCACTT T A SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1390551326 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14850705 RMVar_hsa_circ_92479,RMVar_hsa_circ_217639,RMVar_hsa_circ_372290,RMVar_hsa_circ_217643,RMVar_hsa_circ_217662,RMVar_hsa_circ_87594,RMVar_hsa_circ_72594,RMVar_hsa_circ_68694,RMVar_hsa_circ_81356,RMVar_hsa_circ_217699,RMVar_hsa_circ_357551,RMVar_hsa_circ_217707,RMVar_hsa_circ_366507,RMVar_hsa_circ_338301,RMVar_hsa_circ_365424,RMVar_hsa_circ_339305,RMVar_hsa_circ_293732,RMVar_hsa_circ_217735,RMVar_hsa_circ_307690,RMVar_hsa_circ_279029,RMVar_hsa_circ_217742,RMVar_hsa_circ_122716,RMVar_hsa_circ_322115,RMVar_hsa_circ_217737,RMVar_hsa_circ_217736,RMVar_hsa_circ_217741,RMVar_hsa_circ_270855,RMVar_hsa_circ_217753,RMVar_hsa_circ_217758,RMVar_hsa_circ_217757,RMVar_hsa_circ_287901,RMVar_hsa_circ_285767,RMVar_hsa_circ_217761,RMVar_hsa_circ_92310,RMVar_hsa_circ_285504,RMVar_hsa_circ_217760 29226 RMVar_ID_29226 Human_SNP_ID_132078089 A-to-I Human chr3 - 47767343 47767343 47767343 CCAGCTACTCAGGAGGCCGAGGCAGGAGAATCACTTGAACCCGGGAGGTGGAGTTTATAGTGAGC CCAGCTACTCAGGAGGCCGAGGCAGGAGAATCGCTTGAACCCGGGAGGTGGAGTTTATAGTGAGC T C SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1406468222 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92479,RMVar_hsa_circ_217639,RMVar_hsa_circ_372290,RMVar_hsa_circ_217643,RMVar_hsa_circ_217662,RMVar_hsa_circ_87594,RMVar_hsa_circ_72594,RMVar_hsa_circ_68694,RMVar_hsa_circ_81356,RMVar_hsa_circ_217699,RMVar_hsa_circ_357551,RMVar_hsa_circ_217707,RMVar_hsa_circ_366507,RMVar_hsa_circ_338301,RMVar_hsa_circ_365424,RMVar_hsa_circ_339305,RMVar_hsa_circ_293732,RMVar_hsa_circ_217735,RMVar_hsa_circ_307690,RMVar_hsa_circ_279029,RMVar_hsa_circ_217742,RMVar_hsa_circ_122716,RMVar_hsa_circ_322115,RMVar_hsa_circ_217736,RMVar_hsa_circ_217741,RMVar_hsa_circ_270855,RMVar_hsa_circ_217753,RMVar_hsa_circ_217758,RMVar_hsa_circ_217757,RMVar_hsa_circ_287901,RMVar_hsa_circ_285767,RMVar_hsa_circ_217761,RMVar_hsa_circ_92310,RMVar_hsa_circ_285504,RMVar_hsa_circ_217760 29227 RMVar_ID_29227 Human_SNP_ID_132078200 A-to-I Human chr3 - 47767768 47767768 47767768 TGCCTCCCGGGTTCAAACTATTCTCCTGCCTCAGCCTCCCGAGGACCTGGGATTACAGGCGCCCA TGCCTCCCGGGTTCAAACTATTCTCCTGCCTCGGCCTCCCGAGGACCTGGGATTACAGGCGCCCA T C SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs554546065 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92479,RMVar_hsa_circ_217639,RMVar_hsa_circ_372290,RMVar_hsa_circ_217643,RMVar_hsa_circ_217662,RMVar_hsa_circ_87594,RMVar_hsa_circ_72594,RMVar_hsa_circ_68694,RMVar_hsa_circ_81356,RMVar_hsa_circ_217699,RMVar_hsa_circ_357551,RMVar_hsa_circ_217707,RMVar_hsa_circ_366507,RMVar_hsa_circ_338301,RMVar_hsa_circ_365424,RMVar_hsa_circ_339305,RMVar_hsa_circ_293732,RMVar_hsa_circ_217735,RMVar_hsa_circ_307690,RMVar_hsa_circ_279029,RMVar_hsa_circ_217742,RMVar_hsa_circ_122716,RMVar_hsa_circ_322115,RMVar_hsa_circ_217736,RMVar_hsa_circ_217741,RMVar_hsa_circ_270855,RMVar_hsa_circ_217753,RMVar_hsa_circ_217758,RMVar_hsa_circ_217757,RMVar_hsa_circ_287901,RMVar_hsa_circ_285767,RMVar_hsa_circ_217761,RMVar_hsa_circ_92310,RMVar_hsa_circ_285504,RMVar_hsa_circ_217760 29228 RMVar_ID_29228 Human_SNP_ID_132079310 A-to-I Human chr3 - 47771942 47771942 47771942 GAATAGCTAGGATTACAGGTGCGCGCCACCACACCCAGCTAATTTTTGTATTTTTAGTAGACACA GAATAGCTAGGATTACAGGTGCGCGCCACCACGCCCAGCTAATTTTTGTATTTTTAGTAGACACA T C SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1317133638 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92479,RMVar_hsa_circ_217639,RMVar_hsa_circ_372290,RMVar_hsa_circ_217643,RMVar_hsa_circ_217662,RMVar_hsa_circ_87594,RMVar_hsa_circ_72594,RMVar_hsa_circ_68694,RMVar_hsa_circ_81356,RMVar_hsa_circ_217699,RMVar_hsa_circ_357551,RMVar_hsa_circ_217707,RMVar_hsa_circ_366507,RMVar_hsa_circ_338301,RMVar_hsa_circ_365424,RMVar_hsa_circ_339305,RMVar_hsa_circ_293732,RMVar_hsa_circ_217735,RMVar_hsa_circ_307690,RMVar_hsa_circ_279029,RMVar_hsa_circ_217742,RMVar_hsa_circ_122716,RMVar_hsa_circ_322115,RMVar_hsa_circ_217736,RMVar_hsa_circ_217741,RMVar_hsa_circ_270855,RMVar_hsa_circ_217753,RMVar_hsa_circ_217758,RMVar_hsa_circ_217757,RMVar_hsa_circ_287901,RMVar_hsa_circ_285767,RMVar_hsa_circ_217761,RMVar_hsa_circ_92310,RMVar_hsa_circ_285504,RMVar_hsa_circ_217760 29229 RMVar_ID_29229 Human_SNP_ID_132079326 A-to-I Human chr3 - 47771966 47771966 47771966 CGATTCTTGTGCCTCAAGACTCCCGAATAGCTAGGATTACAGGTGCGCGCCACCACACCCAGCTA CGATTCTTGTGCCTCAAGACTCCCGAATAGCTGGGATTACAGGTGCGCGCCACCACACCCAGCTA T C SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1267553898 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14850925 RMVar_hsa_circ_92479,RMVar_hsa_circ_217639,RMVar_hsa_circ_372290,RMVar_hsa_circ_217643,RMVar_hsa_circ_217662,RMVar_hsa_circ_87594,RMVar_hsa_circ_72594,RMVar_hsa_circ_68694,RMVar_hsa_circ_81356,RMVar_hsa_circ_217699,RMVar_hsa_circ_357551,RMVar_hsa_circ_217707,RMVar_hsa_circ_366507,RMVar_hsa_circ_338301,RMVar_hsa_circ_365424,RMVar_hsa_circ_339305,RMVar_hsa_circ_293732,RMVar_hsa_circ_217735,RMVar_hsa_circ_307690,RMVar_hsa_circ_279029,RMVar_hsa_circ_217742,RMVar_hsa_circ_122716,RMVar_hsa_circ_322115,RMVar_hsa_circ_217736,RMVar_hsa_circ_217741,RMVar_hsa_circ_270855,RMVar_hsa_circ_217753,RMVar_hsa_circ_217758,RMVar_hsa_circ_217757,RMVar_hsa_circ_287901,RMVar_hsa_circ_285767,RMVar_hsa_circ_217761,RMVar_hsa_circ_92310,RMVar_hsa_circ_285504,RMVar_hsa_circ_217760 29230 RMVar_ID_29230 Human_SNP_ID_132080685 A-to-I Human chr3 - 47777020 47777020 47777020 CCTATAATCCCAGCACTTTGGGAGACCGAGGCAGGCGGATCATCTGAGGTTGGGAGTTCGAGACC CCTATAATCCCAGCACTTTGGGAGACCGAGGCGGGCGGATCATCTGAGGTTGGGAGTTCGAGACC T C SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1485240487 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25739845 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 29231 RMVar_ID_29231 Human_SNP_ID_132080736 A-to-I Human chr3 - 47777124 47777124 47777124 TGAGCCGAGATTACGCCACTGCACTCCAGCCTAGGTGACAGAGCAAGACTCTCTCAAAAAAAAAA TGAGCCGAGATTACGCCACTGCACTCCAGCCTGGGTGACAGAGCAAGACTCTCTCAAAAAAAAAA T C SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1559670717 Functional Loss SNV dbSNP153 33..33 33 - - - 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 29232 RMVar_ID_29232 Human_SNP_ID_132080835 A-to-I Human chr3 - 47777430 47777430 47777430 CCTCGTCCTCCCAAAGTACTGGGATTACAGTCATGAGCCACTGCACCCGGCCTATATTCACTGTA CCTCGTCCTCCCAAAGTACTGGGATTACAGTCGTGAGCCACTGCACCCGGCCTATATTCACTGTA T C SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs917945765 Functional Loss SNV dbSNP153 33..33 33 - - - 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 29233 RMVar_ID_29233 Human_SNP_ID_132080893 A-to-I Human chr3 - 47777639 47777639 47777639 ACTGTAGTCCCAGCTACTCAGGAGACTGAGGCAGGAGAATCACTCAAACCTGGGAGGTGGAGGTT ACTGTAGTCCCAGCTACTCAGGAGACTGAGGCGGGAGAATCACTCAAACCTGGGAGGTGGAGGTT T C SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs916186712 Functional Loss SNV dbSNP153 33..33 33 - - - 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 29234 RMVar_ID_29234 Human_SNP_ID_132081142 A-to-I Human chr3 - 47778344 47778344 47778344 TGTTGGCACCATTGCACTCCAGCCTGGGCAACAGAGCGAGACCTTGTCTCAAAACAAAACGAAAC TGTTGGCACCATTGCACTCCAGCCTGGGCAACGGAGCGAGACCTTGTCTCAAAACAAAACGAAAC T C SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1230788425 Functional Loss SNV dbSNP153 33..33 33 - - - 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 29235 RMVar_ID_29235 Human_SNP_ID_132081280 A-to-I Human chr3 - 47778866 47778866 47778866 CTCCCACCTCAGCCTCCTGAGTACCTGGGACTACAGGCACGAACCACCACACCTGGTTAATTTTT CTCCCACCTCAGCCTCCTGAGTACCTGGGACTGCAGGCACGAACCACCACACCTGGTTAATTTTT T C SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs887688982 Functional Loss SNV dbSNP153 33..33 33 - - - 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 29236 RMVar_ID_29236 Human_SNP_ID_132081287 A-to-I Human chr3 - 47778893 47778893 47778893 GCCTCAACCTCCTGGGCTCAGGTGATTCTCCCACCTCAGCCTCCTGAGTACCTGGGACTACAGGC GCCTCAACCTCCTGGGCTCAGGTGATTCTCCCGCCTCAGCCTCCTGAGTACCTGGGACTACAGGC T C SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1187923357 Functional Loss SNV dbSNP153 33..33 33 - - - 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 29237 RMVar_ID_29237 Human_SNP_ID_132081370 A-to-I Human chr3 - 47779196 47779196 47779196 ACAGGGTCTTTCTGTGTTGCCCAGGCTGGAGTACAGTGGCGTGATCATAGCTCACTGCAACCTCA ACAGGGTCTTTCTGTGTTGCCCAGGCTGGAGTGCAGTGGCGTGATCATAGCTCACTGCAACCTCA T C SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1257667222 Functional Loss SNV dbSNP153 33..33 33 - - - 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 29238 RMVar_ID_29238 Human_SNP_ID_132088998 A-to-I Human chr3 + 47806773 47806773 47806773 AGGCGTGCCTGGCCAATTTTTTTTGTATTTTTAGTAGAGACAGGATTTCACCATCTTGGCCAGAA AGGCGTGCCTGGCCAATTTTTTTTGTATTTTTGGTAGAGACAGGATTTCACCATCTTGGCCAGAA A G DHX30 Ensembl:ENSG00000132153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1056219797 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18279,RMVar_hsa_circ_41229,RMVar_hsa_circ_334674,RMVar_hsa_circ_6033 29239 RMVar_ID_29239 Human_SNP_ID_132094340 A-to-I Human chr3 + 47827976 47827976 47827976 AAACTCCTGGGATCAAGTGATCCTCCCGCCTCAGCCTCCAAAGTAGCTGGGACTACAGACAGGTG AAACTCCTGGGATCAAGTGATCCTCCCGCCTCGGCCTCCAAAGTAGCTGGGACTACAGACAGGTG A G DHX30 Ensembl:ENSG00000132153 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs894897675 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14851510 RMVar_hsa_circ_334674,RMVar_hsa_circ_40330,RMVar_hsa_circ_6033,RMVar_hsa_circ_23833,RMVar_hsa_circ_80546,RMVar_hsa_circ_217766,RMVar_hsa_circ_217767,RMVar_hsa_circ_110755,RMVar_hsa_circ_305257,RMVar_hsa_circ_217768 29240 RMVar_ID_29240 Human_SNP_ID_132094342 A-to-I Human chr3 + 47827988 47827988 47827988 TCAAGTGATCCTCCCGCCTCAGCCTCCAAAGTAGCTGGGACTACAGACAGGTGCCACCACACTCG TCAAGTGATCCTCCCGCCTCAGCCTCCAAAGTGGCTGGGACTACAGACAGGTGCCACCACACTCG A G DHX30 Ensembl:ENSG00000132153 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs962921626 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14851510 RMVar_hsa_circ_334674,RMVar_hsa_circ_40330,RMVar_hsa_circ_6033,RMVar_hsa_circ_23833,RMVar_hsa_circ_80546,RMVar_hsa_circ_217766,RMVar_hsa_circ_217767,RMVar_hsa_circ_110755,RMVar_hsa_circ_305257,RMVar_hsa_circ_217768 29241 RMVar_ID_29241 Human_SNP_ID_132094404 A-to-I Human chr3 + 47828218 47828218 47828218 GTGGTGGTTCGTGCCTGTAATCCCAGCACTTTAGGAGGCGGAGTAGGGAGGATCCCTTGAGCCCA GTGGTGGTTCGTGCCTGTAATCCCAGCACTTTGGGAGGCGGAGTAGGGAGGATCCCTTGAGCCCA A G DHX30 Ensembl:ENSG00000132153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1436994221 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_334674,RMVar_hsa_circ_40330,RMVar_hsa_circ_6033,RMVar_hsa_circ_23833,RMVar_hsa_circ_80546,RMVar_hsa_circ_217766,RMVar_hsa_circ_217767,RMVar_hsa_circ_110755,RMVar_hsa_circ_305257,RMVar_hsa_circ_217768 29242 RMVar_ID_29242 Human_SNP_ID_132097578 A-to-I Human chr3 + 47839769 47839769 47839769 CCCATCTCAGCTCACTGCAACCACTGCCTCCCAGGTTCAAGCGATTCTCCTGTCTCAGCCCCCTG CCCATCTCAGCTCACTGCAACCACTGCCTCCCGGGTTCAAGCGATTCTCCTGTCTCAGCCCCCTG A G DHX30 Ensembl:ENSG00000132153 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs375841499 Functional Loss SNV dbSNP153 33..33 33 - - - 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_217769 29243 RMVar_ID_29243 Human_SNP_ID_132103694 A-to-I Human chr3 - 47860979 47860979 47860979 CCTCAAATGATCCACCCGCGTCAGCCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACTGTGC CCTCAAATGATCCACCCGCGTCAGCCCTCCCACAGTGCTGGGATTACAGGTGTGAGCCACTGTGC T G MAP4 Ensembl:ENSG00000047849 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1375482705 Functional Loss SNV dbSNP153 33..33 33 - - - 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 29244 RMVar_ID_29244 Human_SNP_ID_132104710 A-to-I Human chr3 - 47864102 47864102 47864102 TAGGTGGCATGTGCCTGTGGTTCCAGCTTCTCAGGAGGCTGAGAGGGGAGGATTCCTTGAGCCTG TAGGTGGCATGTGCCTGTGGTTCCAGCTTCTCGGGAGGCTGAGAGGGGAGGATTCCTTGAGCCTG T C MAP4 Ensembl:ENSG00000047849 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1226082999 Functional Loss SNV dbSNP153 33..33 33 - - - 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 29245 RMVar_ID_29245 Human_SNP_ID_132109550 A-to-I Human chr3 - 47883506 47883506 47883506 AAAAATATGGAAATAGCCAGGTATGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAG AAAAATATGGAAATAGCCAGGTATGGTGGCTCTTGCCTGTAATCCCAGCACTTTGGGAGGCCAAG T A MAP4 Ensembl:ENSG00000047849 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs942277440 Functional Loss SNV dbSNP153 33..33 33 - - - 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_25071,RMVar_hsa_circ_217791,RMVar_hsa_circ_348035,RMVar_hsa_circ_361244,RMVar_hsa_circ_217794 29246 RMVar_ID_29246 Human_SNP_ID_132109985 A-to-I Human chr3 - 47885347 47885347 47885347 TGATTGATTGATGGTAGAGATGGGATCTTGCTATGTTGCCCAGGCTAGCCTTGACCTCTTGACCT TGATTGATTGATGGTAGAGATGGGATCTTGCTGTGTTGCCCAGGCTAGCCTTGACCTCTTGACCT T C MAP4 Ensembl:ENSG00000047849 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs781455998 Functional Loss SNV dbSNP153 33..33 33 - - - 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_25071,RMVar_hsa_circ_217791,RMVar_hsa_circ_348035,RMVar_hsa_circ_361244,RMVar_hsa_circ_217794 29247 RMVar_ID_29247 Human_SNP_ID_132114193 A-to-I Human chr3 - 47902042 47902042 47902042 TCAAGTAATCCTCCTGCCTCAGCCTCCCAAGTAGTTGAGACTACAGGTGTGCACCACCATACCTG TCAAGTAATCCTCCTGCCTCAGCCTCCCAAGTGGTTGAGACTACAGGTGTGCACCACCATACCTG T C MAP4 Ensembl:ENSG00000047849 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs988758903 Functional Loss SNV dbSNP153 33..33 33 - - - 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_25071,RMVar_hsa_circ_217791,RMVar_hsa_circ_348035,RMVar_hsa_circ_361244,RMVar_hsa_circ_217794 29248 RMVar_ID_29248 Human_SNP_ID_132114201 A-to-I Human chr3 - 47902092 47902092 47902092 TGAAGTGCAGTGGCATGATCACGGCTTACTACAGCCTCGACCTCCCAGGCTCAAGTAATCCTCCT TGAAGTGCAGTGGCATGATCACGGCTTACTACGGCCTCGACCTCCCAGGCTCAAGTAATCCTCCT T C MAP4 Ensembl:ENSG00000047849 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs889123732 Functional Loss SNV dbSNP153 33..33 33 - - - 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_25071,RMVar_hsa_circ_217791,RMVar_hsa_circ_348035,RMVar_hsa_circ_361244,RMVar_hsa_circ_217794 29249 RMVar_ID_29249 Human_SNP_ID_132114545 A-to-I Human chr3 - 47903476 47903474 47903476 AAGGCGAGAGTGCAGTGGCGCGATCTCGGCTCACTGCACGCTCTGCCTCCCAGGTTCACGCCGTT AAGGCGAGAGTGCAGTGGCGCGATCTCGGCTC__TGCACGCTCTGCCTCCCAGGTTCACGCCGTT AGT A MAP4 Ensembl:ENSG00000047849 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1292738540 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_14852981 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_25071,RMVar_hsa_circ_217791,RMVar_hsa_circ_348035,RMVar_hsa_circ_361244,RMVar_hsa_circ_217794 29250 RMVar_ID_29250 Human_SNP_ID_132114738 A-to-I Human chr3 - 47904401 47904401 47904401 AGGCTCAGGAGAATTTCTTGAACCTAGGAGGCAGAGGTTGCAGTGAGCCAAGATCGCACCACTGC AGGCTCAGGAGAATTTCTTGAACCTAGGAGGCTGAGGTTGCAGTGAGCCAAGATCGCACCACTGC T A MAP4 Ensembl:ENSG00000047849 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1230751499 Functional Loss SNV dbSNP153 33..33 33 - - - 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_25071,RMVar_hsa_circ_217791,RMVar_hsa_circ_348035,RMVar_hsa_circ_361244,RMVar_hsa_circ_217794 29251 RMVar_ID_29251 Human_SNP_ID_132114744 A-to-I Human chr3 - 47904436 47904436 47904436 ATGACAGCGCACGCCTGTAATCCCAGCTACTCAGGAGGCTCAGGAGAATTTCTTGAACCTAGGAG ATGACAGCGCACGCCTGTAATCCCAGCTACTCGGGAGGCTCAGGAGAATTTCTTGAACCTAGGAG T C MAP4 Ensembl:ENSG00000047849 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs548501725 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25740183 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_25071,RMVar_hsa_circ_217791,RMVar_hsa_circ_348035,RMVar_hsa_circ_361244,RMVar_hsa_circ_217794 29252 RMVar_ID_29252 Human_SNP_ID_132115293 A-to-I Human chr3 - 47906644 47906644 47906644 AGTTTTGCTCTCATTGCCCACGAAGGAGTGCAATGGCATGATCTCAGTTCACCGCAACCTCTGCC AGTTTTGCTCTCATTGCCCACGAAGGAGTGCAGTGGCATGATCTCAGTTCACCGCAACCTCTGCC T C MAP4 Ensembl:ENSG00000047849 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs994195720 Functional Loss SNV dbSNP153 33..33 33 - - - 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_25071,RMVar_hsa_circ_217791,RMVar_hsa_circ_348035,RMVar_hsa_circ_361244,RMVar_hsa_circ_217794 29253 RMVar_ID_29253 Human_SNP_ID_132118199 A-to-I Human chr3 - 47917499 47917499 47917499 TCATTGCAAACTCCGCCTCCTGGGTTCTAGCAATTCTCCTGCTTCAGCCTCCCAAGTAGCTGGGA TCATTGCAAACTCCGCCTCCTGGGTTCTAGCAGTTCTCCTGCTTCAGCCTCCCAAGTAGCTGGGA T C MAP4 Ensembl:ENSG00000047849 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992934112 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_217783,RMVar_hsa_circ_124585,RMVar_hsa_circ_81267,RMVar_hsa_circ_125095,RMVar_hsa_circ_217787,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_354131,RMVar_hsa_circ_376246,RMVar_hsa_circ_353045,RMVar_hsa_circ_282301,RMVar_hsa_circ_217798,RMVar_hsa_circ_217797,RMVar_hsa_circ_269105,RMVar_hsa_circ_331968 29254 RMVar_ID_29254 Human_SNP_ID_132147486 A-to-I Human chr3 - 48038919 48038919 48038919 TTTTGTATTTTTTGTAGAGACTGGATCTCACCATGTTGCCCAGGCTGATCTTGAACTCCTGGGCT TTTTGTATTTTTTGTAGAGACTGGATCTCACCGTGTTGCCCAGGCTGATCTTGAACTCCTGGGCT T C MAP4 Ensembl:ENSG00000047849 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs537445674 Functional Loss SNV dbSNP153 33..33 33 - - - 29255 RMVar_ID_29255 Human_SNP_ID_132156063 A-to-I Human chr3 - 48068715 48068715 48068715 CAGTGGTGCGATCTTGGCTCACTGCAACCTCCACTTCCTGGGTTCAAGCGATTCTCCTGCCTCTG CAGTGGTGCGATCTTGGCTCACTGCAACCTCCGCTTCCTGGGTTCAAGCGATTCTCCTGCCTCTG T C MAP4 Ensembl:ENSG00000047849 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs970607325 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25740476 29256 RMVar_ID_29256 Human_SNP_ID_132156379 A-to-I Human chr3 - 48070308 48070308 48070308 AAAAGAAACCGTGGTTGGGCATGGTGGCTCACACTTGTAATCCCAGCACTTTGGGAGGCTGAGGT AAAAGAAACCGTGGTTGGGCATGGTGGCTCACCCTTGTAATCCCAGCACTTTGGGAGGCTGAGGT T G MAP4 Ensembl:ENSG00000047849 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1452651637 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_212866 29257 RMVar_ID_29257 Human_SNP_ID_132158805 A-to-I Human chr3 - 48079424 48079424 48079424 GTCTTGAACTCCTGACCTCAAGTGATGCGCCCACCTTGGCCTGCCAAAGTGCTGGGATTACAGAC GTCTTGAACTCCTGACCTCAAGTGATGCGCCCGCCTTGGCCTGCCAAAGTGCTGGGATTACAGAC T C MAP4 Ensembl:ENSG00000047849 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202382775 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8574014,Human_RBP_ID_14855214 29258 RMVar_ID_29258 Human_SNP_ID_132159310 A-to-I Human chr3 - 48081168 48081168 48081168 CTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCGCCTGCCACCACTCCCGGCTAATGTTT CTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTGCAGGCGCCTGCCACCACTCCCGGCTAATGTTT T C MAP4 Ensembl:ENSG00000047849 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs993853323 Functional Loss SNV dbSNP153 33..33 33 - - - 29259 RMVar_ID_29259 Human_SNP_ID_132159849 A-to-I Human chr3 - 48083494 48083494 48083494 GGGCCTGGTGGCGGGCGCCTGTAATCCCAGCTACTCGGGAAGCTGAGGCAGGAGAATCACTTGAA GGGCCTGGTGGCGGGCGCCTGTAATCCCAGCTGCTCGGGAAGCTGAGGCAGGAGAATCACTTGAA T C MAP4 Ensembl:ENSG00000047849 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1476480707 Functional Loss SNV dbSNP153 33..33 33 - - - 29260 RMVar_ID_29260 Human_SNP_ID_132169434 A-to-I Human chr3 - 48121208 48121208 48121208 AAGCAGCCTGAGGTAATCTGTGAAAATGGTTCACTATTCACTTGACCCAGAGAACCCCGCAAAAT AAGCAGCCTGAGGTAATCTGTGAAAATGGTTCGCTATTCACTTGACCCAGAGAACCCCGCAAAAT T C AC124916.1 Ensembl:ENSG00000236768 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1410697961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1858333 29261 RMVar_ID_29261 Human_SNP_ID_132179319 A-to-I Human chr3 - 48160575 48160575 48160575 GAAATCCCGTCTCTACTAAAAATACAAAAATTAGCCAGGCGTGGTGGCGGACACCTGTAATCCCA GAAATCCCGTCTCTACTAAAAATACAAAAATTTGCCAGGCGTGGTGGCGGACACCTGTAATCCCA T A CDC25A Ensembl:ENSG00000164045 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1045705887 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48846,RMVar_hsa_circ_118086,RMVar_hsa_circ_217814 29262 RMVar_ID_29262 Human_SNP_ID_132179423 A-to-I Human chr3 - 48161031 48161031 48161031 TCTCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCACCTGCCACCACGCCCAGCTAATTTTT TCTCTGCCTCAGCCTCCCAAGTAGCTGGGATTCCAGGCACCTGCCACCACGCCCAGCTAATTTTT T G CDC25A Ensembl:ENSG00000164045 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1046185593 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48846,RMVar_hsa_circ_118086,RMVar_hsa_circ_217814 29263 RMVar_ID_29263 Human_SNP_ID_132179581 A-to-I Human chr3 - 48161545 48161545 48161545 ATCACCATGCCTGGCTAATTTTTGTATTTTTTATAGAGACAGGGTCTCACTGTGTTGCCCAGGCT ATCACCATGCCTGGCTAATTTTTGTATTTTTTGTAGAGACAGGGTCTCACTGTGTTGCCCAGGCT T C CDC25A Ensembl:ENSG00000164045 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs563164638 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48846,RMVar_hsa_circ_118086,RMVar_hsa_circ_217814 29264 RMVar_ID_29264 Human_SNP_ID_132179814 A-to-I Human chr3 - 48162348 48162348 48162348 CCAGCAGGTCGAGGCTGTGGTGAGCCATGATCATGCCACTGTACTCCAGCCTAGGTGACAGAGTG CCAGCAGGTCGAGGCTGTGGTGAGCCATGATCCTGCCACTGTACTCCAGCCTAGGTGACAGAGTG T G CDC25A Ensembl:ENSG00000164045 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1212326533 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25740610 RMVar_hsa_circ_48846,RMVar_hsa_circ_118086,RMVar_hsa_circ_217814 29265 RMVar_ID_29265 Human_SNP_ID_132181948 A-to-I Human chr3 - 48170695 48170695 48170695 AGAGGTTGGAACTTTCAGCCCCACCCTCCAATATCTACGGAAAGGAGAGGGGCTAAAGGTCAAGT AGAGGTTGGAACTTTCAGCCCCACCCTCCAATGTCTACGGAAAGGAGAGGGGCTAAAGGTCAAGT T C CDC25A Ensembl:ENSG00000164045 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs3731532 Functional Loss SNV dbSNP153,EGP 33..33 33 - - - GWAS_ID_3224,GWAS_ID_3225,GWAS_ID_3226,GWAS_ID_3227,GWAS_ID_3228,GWAS_ID_3229,GWAS_ID_3230,GWAS_ID_3231,GWAS_ID_3232,GWAS_ID_3233,GWAS_ID_3234,GWAS_ID_3235,GWAS_ID_3236,GWAS_ID_3237,GWAS_ID_3238,GWAS_ID_3239 RMVar_hsa_circ_48846,RMVar_hsa_circ_62055,RMVar_hsa_circ_14310,RMVar_hsa_circ_96716,RMVar_hsa_circ_27018,RMVar_hsa_circ_217815,RMVar_hsa_circ_316186,RMVar_hsa_circ_217816,RMVar_hsa_circ_37123,RMVar_hsa_circ_277796 29266 RMVar_ID_29266 Human_SNP_ID_132201901 A-to-I Human chr3 + 48250533 48250533 48250533 TCCCTCTGTTGCCCACGCTGGAGTACAGTGATACGATCTTGGCTCACTGCAATCTCCGTCTCCTG TCCCTCTGTTGCCCACGCTGGAGTACAGTGATGCGATCTTGGCTCACTGCAATCTCCGTCTCCTG A G ZNF589 Ensembl:ENSG00000164048 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1334695254 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_335024 29267 RMVar_ID_29267 Human_SNP_ID_132201908 A-to-I Human chr3 + 48250611 48250569 48250611 CTCCTGCTTCAGCCTCCTGAGAAGCTGGGATTACAAGCATGCGACACCACGCCTGGCTAATTTTT _________________________________CAAGCATGCGACACCACGCCTGGCTAATTTTT TCAAGTGATTCTCCTGCTTCAGCCTCCTGAGAAGCTGGGATTA T ZNF589 Ensembl:ENSG00000164048 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs554073028 Functional Loss DEL dbSNP153 1..33 33 - - - RMVar_hsa_circ_335024 29268 RMVar_ID_29268 Human_SNP_ID_132201921 A-to-I Human chr3 + 48250611 48250610 48250611 CTCCTGCTTCAGCCTCCTGAGAAGCTGGGATTACAAGCATGCGACACCACGCCTGGCTAATTTTT CTCCTGCTTCAGCCTCCTGAGAAGCTGGGATT_CAAGCATGCGACACCACGCCTGGCTAATTTTT TA T ZNF589 Ensembl:ENSG00000164048 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs763624694 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_335024 29269 RMVar_ID_29269 Human_SNP_ID_132202481 A-to-I Human chr3 + 48252740 48252740 48252740 GCCCCCTGGGGTTCACGCCATTCTCTTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCCACTG GCCCCCTGGGGTTCACGCCATTCTCTTGCCTCGGCCTCCCAAGTAGCTGGGACTACAGGCCACTG A G ZNF589 Ensembl:ENSG00000164048 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs887825522 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_335024 29270 RMVar_ID_29270 Human_SNP_ID_132202577 A-to-I Human chr3 + 48253216 48253216 48253216 CACTACACATAGCTATTTTTTGTATTTTTAGTAGATGGGCTTTTGCCACGTTGGCCAGGCTGGTC CACTACACATAGCTATTTTTTGTATTTTTAGTTGATGGGCTTTTGCCACGTTGGCCAGGCTGGTC A T ZNF589 Ensembl:ENSG00000164048 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1485590094 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14856511 RMVar_hsa_circ_335024 29271 RMVar_ID_29271 Human_SNP_ID_132202766 A-to-I Human chr3 + 48253964 48253964 48253964 AATTAAGAAATTTGCTGGGATTGGTGGCATGTACCTGTATCCTAGCTACTTGGGAGGCTGCCGTG AATTAAGAAATTTGCTGGGATTGGTGGCATGTGCCTGTATCCTAGCTACTTGGGAGGCTGCCGTG A G ZNF589 Ensembl:ENSG00000164048 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs761625837 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14856526 RMVar_hsa_circ_335024 29272 RMVar_ID_29272 Human_SNP_ID_132246671 A-to-I Human chr3 - 48438243 48438243 48438243 GTGTACAATTCAGTGGTTTTATTATATTCACAAAGTTGTATGGCCATCACCAAAATAAATTTTTT GTGTACAATTCAGTGGTTTTATTATATTCACAGAGTTGTATGGCCATCACCAAAATAAATTTTTT T C CCDC51 Ensembl:ENSG00000164051 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1351695402 Functional Loss SNV dbSNP153 33..33 33 - - - 29273 RMVar_ID_29273 Human_SNP_ID_132246673 A-to-I Human chr3 - 48438252 48438252 48438252 TCATGCAATGTGTACAATTCAGTGGTTTTATTATATTCACAAAGTTGTATGGCCATCACCAAAAT TCATGCAATGTGTACAATTCAGTGGTTTTATTGTATTCACAAAGTTGTATGGCCATCACCAAAAT T C CCDC51 Ensembl:ENSG00000164051 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs546953787 Functional Loss SNV dbSNP153 33..33 33 - - - 29274 RMVar_ID_29274 Human_SNP_ID_132247022 A-to-I Human chr3 - 48439717 48439717 48439717 TTTTGGTGATGGCCATACAACTCTGTTAATATAGTAAAACTACTGAATTGTACACATTGGGTGAA TTTTGGTGATGGCCATACAACTCTGTTAATATTGTAAAACTACTGAATTGTACACATTGGGTGAA T A CCDC51 Ensembl:ENSG00000164051 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1480663918 Functional Loss SNV dbSNP153 33..33 33 - - - 29275 RMVar_ID_29275 Human_SNP_ID_132247023 A-to-I Human chr3 - 48439717 48439717 48439717 TTTTGGTGATGGCCATACAACTCTGTTAATATAGTAAAACTACTGAATTGTACACATTGGGTGAA TTTTGGTGATGGCCATACAACTCTGTTAATATGGTAAAACTACTGAATTGTACACATTGGGTGAA T C CCDC51 Ensembl:ENSG00000164051 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1480663918 Functional Loss SNV dbSNP153 33..33 33 - - - 29276 RMVar_ID_29276 Human_SNP_ID_132248239 A-to-I Human chr3 + 48442993 48442993 48442993 TGGGCATGGTGGCTCAAGACTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGTGGACCACTTGA TGGGCATGGTGGCTCAAGACTGTAATCCCAGCGCTTTGGGAGGCTGAGGTGGGTGGACCACTTGA A G TMA7 Ensembl:ENSG00000232112 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1382453119 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22608080 29277 RMVar_ID_29277 Human_SNP_ID_132250496 A-to-I Human chr3 + 48450650 48450650 48450650 AGTCTGTCATCCAGGCTGGAGTACAGTGACACAATCTTGGCTCACTTCAACCTCTGCCTCCTGGT AGTCTGTCATCCAGGCTGGAGTACAGTGACACCATCTTGGCTCACTTCAACCTCTGCCTCCTGGT A C ATRIP Ensembl:ENSG00000164053 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1361026101 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3867,RMVar_hsa_circ_302730,RMVar_hsa_circ_336135,RMVar_hsa_circ_273957,RMVar_hsa_circ_42281,RMVar_hsa_circ_217851 29278 RMVar_ID_29278 Human_SNP_ID_132250521 A-to-I Human chr3 + 48450770 48450770 48450770 CACGACGCCCAGCTAATTCTTGTATTTTTAGTAGAGACGGAGTTTCACCATGTTGGCCAGGCTGG CACGACGCCCAGCTAATTCTTGTATTTTTAGTGGAGACGGAGTTTCACCATGTTGGCCAGGCTGG A G ATRIP Ensembl:ENSG00000164053 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1380510304 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3867,RMVar_hsa_circ_302730,RMVar_hsa_circ_336135,RMVar_hsa_circ_273957,RMVar_hsa_circ_42281,RMVar_hsa_circ_217851 29279 RMVar_ID_29279 Human_SNP_ID_132253260 A-to-I Human chr3 + 48462072 48462072 48462072 ATCCCAGGCTGGGCACAGTGGCTCCTGCCTGTAATCTCAGCACTTTGGGAGGCCAAGGTGGGAGG ATCCCAGGCTGGGCACAGTGGCTCCTGCCTGTCATCTCAGCACTTTGGGAGGCCAAGGTGGGAGG A C ATRIP Ensembl:ENSG00000164053 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs961423772 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3867,RMVar_hsa_circ_98528,RMVar_hsa_circ_217854 29280 RMVar_ID_29280 Human_SNP_ID_132253305 A-to-I Human chr3 + 48462235 48462235 48462235 TGAGCTATGACCATGCCACTGCACTCCAGCCTAGGTGACAGAGTGAGACCCTATCTCAAAGAATC TGAGCTATGACCATGCCACTGCACTCCAGCCTGGGTGACAGAGTGAGACCCTATCTCAAAGAATC A G ATRIP Ensembl:ENSG00000164053 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223796420 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3867,RMVar_hsa_circ_98528,RMVar_hsa_circ_217854 29281 RMVar_ID_29281 Human_SNP_ID_132255401 A-to-I Human chr3 - 48468744 48468744 48468744 GGCACATCTGGAGTTCTTCTCCAGCTTACCCTAGGGTGACCAAGTAGGGCCTGTCACACCAGGGT GGCACATCTGGAGTTCTTCTCCAGCTTACCCTGGGGTGACCAAGTAGGGCCTGTCACACCAGGGT T C SHISA5 Ensembl:ENSG00000164054 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs754738725 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_603487,Human_RBP_ID_17661384,Human_RBP_ID_24006602,Human_RBP_ID_26510315,Human_RBP_ID_27566308 29282 RMVar_ID_29282 Human_SNP_ID_132256084 A-to-I Human chr3 - 48470840 48470840 48470840 TGAATGCAACCTCTGCCTCTCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGA TGAATGCAACCTCTGCCTCTCGGGTTCAAGCGGTTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGA T C SHISA5 Ensembl:ENSG00000164054 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1403388496 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_351627 29283 RMVar_ID_29283 Human_SNP_ID_132256170 A-to-I Human chr3 - 48471218 48471218 48471218 CTTGAGGCCAGGAGTTGGAAACCAGTTAGGTAACATAGTGAGACCCCTGTCTCTGCAAAAATAAA CTTGAGGCCAGGAGTTGGAAACCAGTTAGGTAGCATAGTGAGACCCCTGTCTCTGCAAAAATAAA T C SHISA5 Ensembl:ENSG00000164054 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs939824318 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_351627 29284 RMVar_ID_29284 Human_SNP_ID_132271756 A-to-I Human chr3 - 48532640 48532640 48532640 CACTATATTGCCCAGGTTGGTCTCAAACTCCTAGCCTCAAGCGATTCTACCACTTTGGCCTCTCA CACTATATTGCCCAGGTTGGTCTCAAACTCCTCGCCTCAAGCGATTCTACCACTTTGGCCTCTCA T G PFKFB4 Ensembl:ENSG00000114268 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1481277130 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17573617 RMVar_hsa_circ_338662,RMVar_hsa_circ_267763 29285 RMVar_ID_29285 Human_SNP_ID_132271759 A-to-I Human chr3 - 48532666 48532666 48532666 TTTATTTTTTGTAGAGAAGGGAGGCTCACTATATTGCCCAGGTTGGTCTCAAACTCCTAGCCTCA TTTATTTTTTGTAGAGAAGGGAGGCTCACTATGTTGCCCAGGTTGGTCTCAAACTCCTAGCCTCA T C PFKFB4 Ensembl:ENSG00000114268 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs978804211 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17573617 RMVar_hsa_circ_338662,RMVar_hsa_circ_267763 29286 RMVar_ID_29286 Human_SNP_ID_132272009 A-to-I Human chr3 - 48533866 48533866 48533866 TAAAAACAGTTGTTTGATTTGTCCCTTTATTTATTTATTTTTTTGAGACGGAGGTTTGCTCCTGT TAAAAACAGTTGTTTGATTTGTCCCTTTATTTGTTTATTTTTTTGAGACGGAGGTTTGCTCCTGT T C PFKFB4 Ensembl:ENSG00000114268 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1429315934 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_338662,RMVar_hsa_circ_267763 29287 RMVar_ID_29287 Human_SNP_ID_132272152 A-to-I Human chr3 - 48534614 48534614 48534614 CAAGCTGGAGTGCTGTGGTGCAATCATAGCTCACTGTAGCCTCAACTTCCTGGGCTCAAGCCATC CAAGCTGGAGTGCTGTGGTGCAATCATAGCTCGCTGTAGCCTCAACTTCCTGGGCTCAAGCCATC T C PFKFB4 Ensembl:ENSG00000114268 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459350770 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17573621 RMVar_hsa_circ_338662,RMVar_hsa_circ_267763 29288 RMVar_ID_29288 Human_SNP_ID_132272154 A-to-I Human chr3 - 48534619 48534619 48534619 TCACCCAAGCTGGAGTGCTGTGGTGCAATCATAGCTCACTGTAGCCTCAACTTCCTGGGCTCAAG TCACCCAAGCTGGAGTGCTGTGGTGCAATCATGGCTCACTGTAGCCTCAACTTCCTGGGCTCAAG T C PFKFB4 Ensembl:ENSG00000114268 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1170603529 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17573621 RMVar_hsa_circ_338662,RMVar_hsa_circ_267763 29289 RMVar_ID_29289 Human_SNP_ID_132272259 A-to-I Human chr3 - 48534997 48534997 48534997 TGAGTCCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTGAAAATACAAAAATTAGCCAGGCA TGAGTCCAGCCTGGCCAACATGGTGAAACCCCGTCTCTACTGAAAATACAAAAATTAGCCAGGCA T C PFKFB4 Ensembl:ENSG00000114268 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1289806304 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_338662,RMVar_hsa_circ_267763 29290 RMVar_ID_29290 Human_SNP_ID_132272262 A-to-I Human chr3 - 48535010 48535010 48535010 CAAGTCAGGAGTTTGAGTCCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTGAAAATACAAA CAAGTCAGGAGTTTGAGTCCAGCCTGGCCAACCTGGTGAAACCCCATCTCTACTGAAAATACAAA T G PFKFB4 Ensembl:ENSG00000114268 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1320655804 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_338662,RMVar_hsa_circ_267763 29291 RMVar_ID_29291 Human_SNP_ID_132273989 A-to-I Human chr3 - 48541844 48541844 48541844 CTCACACCTCAGCCTCCTGAGTAGCTGGGACTACAGGCACGTGCCACCATGCTTGGCTAATTCTT CTCACACCTCAGCCTCCTGAGTAGCTGGGACTTCAGGCACGTGCCACCATGCTTGGCTAATTCTT T A PFKFB4 Ensembl:ENSG00000114268 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs528923248 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91442,RMVar_hsa_circ_342416,RMVar_hsa_circ_336260,RMVar_hsa_circ_217857,RMVar_hsa_circ_217858,RMVar_hsa_circ_27720,RMVar_hsa_circ_7278,RMVar_hsa_circ_217861,RMVar_hsa_circ_277032,RMVar_hsa_circ_25120,RMVar_hsa_circ_88456,RMVar_hsa_circ_217862 29292 RMVar_ID_29292 Human_SNP_ID_132277081 A-to-I Human chr3 - 48554963 48554963 48554963 TCACTGCAACCTCTACCTCCTGGGTTCAAGCAATTCTCCTGCCTCAGCCTTCCAAGTTGCTGGGA TCACTGCAACCTCTACCTCCTGGGTTCAAGCAGTTCTCCTGCCTCAGCCTTCCAAGTTGCTGGGA T C PFKFB4 Ensembl:ENSG00000114268 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1473244818 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91442,RMVar_hsa_circ_217857,RMVar_hsa_circ_94147,RMVar_hsa_circ_217866 29293 RMVar_ID_29293 Human_SNP_ID_132277082 A-to-I Human chr3 - 48554964 48554964 48554964 CTCACTGCAACCTCTACCTCCTGGGTTCAAGCAATTCTCCTGCCTCAGCCTTCCAAGTTGCTGGG CTCACTGCAACCTCTACCTCCTGGGTTCAAGCCATTCTCCTGCCTCAGCCTTCCAAGTTGCTGGG T G PFKFB4 Ensembl:ENSG00000114268 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1014413432 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91442,RMVar_hsa_circ_217857,RMVar_hsa_circ_94147,RMVar_hsa_circ_217866 29294 RMVar_ID_29294 Human_SNP_ID_132312719 A-to-I Human chr3 - 48670827 48670826 48670827 AAGACCCCATCCCTACAAAAAATACAAAAATTAGCTGGGCGTGGTGGCCCACACCTGTAGTCCTA AAGACCCCATCCCTACAAAAAATACAAAAATT_GCTGGGCGTGGTGGCCCACACCTGTAGTCCTA CT C lnc-NCKIPSD-1 RNACentral:URS00008B560A lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1367642460 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_113259,RMVar_hsa_circ_217965 29295 RMVar_ID_29295 Human_SNP_ID_132312721 A-to-I Human chr3 - 48670827 48670827 48670827 AAGACCCCATCCCTACAAAAAATACAAAAATTAGCTGGGCGTGGTGGCCCACACCTGTAGTCCTA AAGACCCCATCCCTACAAAAAATACAAAAATTGGCTGGGCGTGGTGGCCCACACCTGTAGTCCTA T C lnc-NCKIPSD-1 RNACentral:URS00008B560A lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs752483121 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113259,RMVar_hsa_circ_217965 29296 RMVar_ID_29296 Human_SNP_ID_132314266 A-to-I Human chr3 - 48676712 48676712 48676712 GAAGTGGGAGGATCACTTGAGTCCATGAGTTCAAGATCAGCCTGGGCAACATAGTGAGACCTCTG GAAGTGGGAGGATCACTTGAGTCCATGAGTTCGAGATCAGCCTGGGCAACATAGTGAGACCTCTG T C NCKIPSD Ensembl:ENSG00000213672 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs921862017 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14858608 RMVar_hsa_circ_102002,RMVar_hsa_circ_217968 29297 RMVar_ID_29297 Human_SNP_ID_132314318 A-to-I Human chr3 - 48676908 48676908 48676908 AAATTAGCTGGGTATGGTGGTGGGAGCCTGTAATCCCACCTACTTGGGAGGCTGAGGCAGGAGAA AAATTAGCTGGGTATGGTGGTGGGAGCCTGTAGTCCCACCTACTTGGGAGGCTGAGGCAGGAGAA T C NCKIPSD Ensembl:ENSG00000213672 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1033216075 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102002,RMVar_hsa_circ_217968 29298 RMVar_ID_29298 Human_SNP_ID_132314341 A-to-I Human chr3 - 48676969 48676969 48676969 AATTCGAGACCAGCCTGGTCAAAGTGGTCTCTACTAAAAATACAAAATACGAAAAATACAAAAAT AATTCGAGACCAGCCTGGTCAAAGTGGTCTCTGCTAAAAATACAAAATACGAAAAATACAAAAAT T C NCKIPSD Ensembl:ENSG00000213672 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs931932521 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17573632,Human_RBP_ID_23189461 RMVar_hsa_circ_102002,RMVar_hsa_circ_217968 29299 RMVar_ID_29299 Human_SNP_ID_132314346 A-to-I Human chr3 - 48677000 48677000 48677000 GGCTGAGGTGGGTGGATCACTTGAGGTCAGGAATTCGAGACCAGCCTGGTCAAAGTGGTCTCTAC GGCTGAGGTGGGTGGATCACTTGAGGTCAGGAGTTCGAGACCAGCCTGGTCAAAGTGGTCTCTAC T C NCKIPSD Ensembl:ENSG00000213672 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1308012680 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17573632 RMVar_hsa_circ_102002,RMVar_hsa_circ_217968 29300 RMVar_ID_29300 Human_SNP_ID_132314397 A-to-I Human chr3 - 48677217 48677217 48677217 CACCCAGCTAATTTTTATATTTTAGCAGAGACAGGGTTTCGCCATGTTGGCCAGGCTGGTCTTGA CACCCAGCTAATTTTTATATTTTAGCAGAGACGGGGTTTCGCCATGTTGGCCAGGCTGGTCTTGA T C NCKIPSD Ensembl:ENSG00000213672 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs764624653 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18007029 RMVar_hsa_circ_102002,RMVar_hsa_circ_217968 29301 RMVar_ID_29301 Human_SNP_ID_132314402 A-to-I Human chr3 - 48677233 48677233 48677233 CAGTCACCCACTACCACACCCAGCTAATTTTTATATTTTAGCAGAGACAGGGTTTCGCCATGTTG CAGTCACCCACTACCACACCCAGCTAATTTTTTTATTTTAGCAGAGACAGGGTTTCGCCATGTTG T A NCKIPSD Ensembl:ENSG00000213672 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs565340204 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18007029 RMVar_hsa_circ_102002,RMVar_hsa_circ_217968 29302 RMVar_ID_29302 Human_SNP_ID_132314403 A-to-I Human chr3 - 48677233 48677233 48677233 CAGTCACCCACTACCACACCCAGCTAATTTTTATATTTTAGCAGAGACAGGGTTTCGCCATGTTG CAGTCACCCACTACCACACCCAGCTAATTTTTGTATTTTAGCAGAGACAGGGTTTCGCCATGTTG T C NCKIPSD Ensembl:ENSG00000213672 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs565340204 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18007029 RMVar_hsa_circ_102002,RMVar_hsa_circ_217968 29303 RMVar_ID_29303 Human_SNP_ID_132314415 A-to-I Human chr3 - 48677264 48677264 48677264 CCTGCCTCAGCCTCCCAAGTTGCTGGGATTACAGTCACCCACTACCACACCCAGCTAATTTTTAT CCTGCCTCAGCCTCCCAAGTTGCTGGGATTACTGTCACCCACTACCACACCCAGCTAATTTTTAT T A NCKIPSD Ensembl:ENSG00000213672 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1248411126 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102002,RMVar_hsa_circ_217968 29304 RMVar_ID_29304 Human_SNP_ID_132314417 A-to-I Human chr3 - 48677279 48677279 48677279 GTTTCAAGTGATTCTCCTGCCTCAGCCTCCCAAGTTGCTGGGATTACAGTCACCCACTACCACAC GTTTCAAGTGATTCTCCTGCCTCAGCCTCCCAGGTTGCTGGGATTACAGTCACCCACTACCACAC T C NCKIPSD Ensembl:ENSG00000213672 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs940575272 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102002,RMVar_hsa_circ_217968 29305 RMVar_ID_29305 Human_SNP_ID_132320466 A-to-I Human chr3 - 48697426 48697426 48697426 AGCTACTTGGGAGGTTGTGGCAGGAGAATCGCATGAGACTGGGAGGCAGAGGTTGCAGTGAACTG AGCTACTTGGGAGGTTGTGGCAGGAGAATCGCGTGAGACTGGGAGGCAGAGGTTGCAGTGAACTG T C IP6K2 Ensembl:ENSG00000068745 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1416940569 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14858952 RMVar_hsa_circ_82807,RMVar_hsa_circ_217975 29306 RMVar_ID_29306 Human_SNP_ID_132320470 A-to-I Human chr3 - 48697431 48697431 48697431 GTCCCAGCTACTTGGGAGGTTGTGGCAGGAGAATCGCATGAGACTGGGAGGCAGAGGTTGCAGTG GTCCCAGCTACTTGGGAGGTTGTGGCAGGAGAGTCGCATGAGACTGGGAGGCAGAGGTTGCAGTG T C IP6K2 Ensembl:ENSG00000068745 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1247081420 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14858952,Human_RBP_ID_25741038 RMVar_hsa_circ_82807,RMVar_hsa_circ_217975 29307 RMVar_ID_29307 Human_SNP_ID_132320471 A-to-I Human chr3 - 48697431 48697431 48697431 GTCCCAGCTACTTGGGAGGTTGTGGCAGGAGAATCGCATGAGACTGGGAGGCAGAGGTTGCAGTG GTCCCAGCTACTTGGGAGGTTGTGGCAGGAGACTCGCATGAGACTGGGAGGCAGAGGTTGCAGTG T G IP6K2 Ensembl:ENSG00000068745 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1247081420 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14858952,Human_RBP_ID_25741038 RMVar_hsa_circ_82807,RMVar_hsa_circ_217975 29308 RMVar_ID_29308 Human_SNP_ID_132320478 A-to-I Human chr3 - 48697464 48697464 48697464 AAAAAAAATAGCCAGGCATGGTGGGTGCCTGTAGTCCCAGCTACTTGGGAGGTTGTGGCAGGAGA AAAAAAAATAGCCAGGCATGGTGGGTGCCTGTTGTCCCAGCTACTTGGGAGGTTGTGGCAGGAGA T A IP6K2 Ensembl:ENSG00000068745 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1294075941 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82807,RMVar_hsa_circ_217975 29309 RMVar_ID_29309 Human_SNP_ID_132320940 A-to-I Human chr3 - 48699248 48699248 48699248 GCGCCACCACACCCAGCTGATTTTGTATTTTTAGTAGAGACAGCATTTCTCTATGTTGGTCAGGC GCGCCACCACACCCAGCTGATTTTGTATTTTTGGTAGAGACAGCATTTCTCTATGTTGGTCAGGC T C IP6K2 Ensembl:ENSG00000068745 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1052210308 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14859008 RMVar_hsa_circ_82807,RMVar_hsa_circ_217975 29310 RMVar_ID_29310 Human_SNP_ID_132320941 A-to-I Human chr3 - 48699248 48699248 48699248 GCGCCACCACACCCAGCTGATTTTGTATTTTTAGTAGAGACAGCATTTCTCTATGTTGGTCAGGC GCGCCACCACACCCAGCTGATTTTGTATTTTTCGTAGAGACAGCATTTCTCTATGTTGGTCAGGC T G IP6K2 Ensembl:ENSG00000068745 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1052210308 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14859008 RMVar_hsa_circ_82807,RMVar_hsa_circ_217975 29311 RMVar_ID_29311 Human_SNP_ID_132322802 A-to-I Human chr3 - 48706683 48706683 48706683 GGCCCGTGCCACTACGCCCAGCTAGTTTTTGTATTTTTAGTGGAGATGGGGTTTTGCCATGTTGC GGCCCGTGCCACTACGCCCAGCTAGTTTTTGTGTTTTTAGTGGAGATGGGGTTTTGCCATGTTGC T C IP6K2 Ensembl:ENSG00000068745 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1356144708 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25741079 RMVar_hsa_circ_82807,RMVar_hsa_circ_217975 29312 RMVar_ID_29312 Human_SNP_ID_132322805 A-to-I Human chr3 - 48706696 48706696 48706696 AGCTGGGACTATGGGCCCGTGCCACTACGCCCAGCTAGTTTTTGTATTTTTAGTGGAGATGGGGT AGCTGGGACTATGGGCCCGTGCCACTACGCCCGGCTAGTTTTTGTATTTTTAGTGGAGATGGGGT T C IP6K2 Ensembl:ENSG00000068745 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs965103476 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82807,RMVar_hsa_circ_217975 29313 RMVar_ID_29313 Human_SNP_ID_132323142 A-to-I Human chr3 - 48708123 48708123 48708123 CTTCCATCTCAGCCTCCCAAGTAGCTGGGACCACAGGTATGCGCCATTGCACCTGGCTATTTTTT CTTCCATCTCAGCCTCCCAAGTAGCTGGGACCGCAGGTATGCGCCATTGCACCTGGCTATTTTTT T C IP6K2 Ensembl:ENSG00000068745 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1433237891 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_426123,Human_Splice_Rec_426179,Human_Splice_Rec_426221,Human_Splice_Rec_426227 RMVar_hsa_circ_82807,RMVar_hsa_circ_217975 29314 RMVar_ID_29314 Human_SNP_ID_132323348 A-to-I Human chr3 - 48708900 48708900 48708900 CCACACCTGGCTGGTTATTTTTTGTAGAGACAAGGTCTCACTATTTTGCCAGGATTGTTCTCAAA CCACACCTGGCTGGTTATTTTTTGTAGAGACAGGGTCTCACTATTTTGCCAGGATTGTTCTCAAA T C IP6K2 Ensembl:ENSG00000068745 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1043021863 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14859390,Human_RBP_ID_24007005 RMVar_hsa_circ_82807,RMVar_hsa_circ_217975 29315 RMVar_ID_29315 Human_SNP_ID_132323646 A-to-I Human chr3 - 48710207 48710207 48710207 TTTTAAAACATTTTTTGTGAAGACAGGGTCTCACTGTGTTGCCCAGGCTGGTCTCAAACTTCTGA TTTTAAAACATTTTTTGTGAAGACAGGGTCTCGCTGTGTTGCCCAGGCTGGTCTCAAACTTCTGA T C IP6K2 Ensembl:ENSG00000068745 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355064630 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82807,RMVar_hsa_circ_217975 29316 RMVar_ID_29316 Human_SNP_ID_132323660 A-to-I Human chr3 - 48710274 48710274 48710274 GTGATCCTCCTGCCTCAGCCTTCTGAGTAGCTAGGACTACAGGCGCATGCCACCAAGCCTGGCTA GTGATCCTCCTGCCTCAGCCTTCTGAGTAGCTGGGACTACAGGCGCATGCCACCAAGCCTGGCTA T C IP6K2 Ensembl:ENSG00000068745 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1051511911 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82807,RMVar_hsa_circ_217975 29317 RMVar_ID_29317 Human_SNP_ID_132324285 A-to-I Human chr3 - 48712834 48712834 48712834 TAATTGTATTTTTGTAGTGATGGGTTTTCACCATGTTGTCCAGGCTGGTCTCGAACTCCTGACCT TAATTGTATTTTTGTAGTGATGGGTTTTCACCGTGTTGTCCAGGCTGGTCTCGAACTCCTGACCT T C IP6K2 Ensembl:ENSG00000068745 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs952115364 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25741121 RMVar_hsa_circ_82807,RMVar_hsa_circ_217975 29318 RMVar_ID_29318 Human_SNP_ID_132324713 A-to-I Human chr3 - 48714455 48714455 48714455 CCAGGGGGTGGAGATTGCAGTGAGCCAAAATCACACCACTGCACTCCCGCCTGGGCGACAGAGTG CCAGGGGGTGGAGATTGCAGTGAGCCAAAATCGCACCACTGCACTCCCGCCTGGGCGACAGAGTG T C IP6K2 Ensembl:ENSG00000068745 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7623695 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25770829 RMVar_hsa_circ_82807,RMVar_hsa_circ_217975 29319 RMVar_ID_29319 Human_SNP_ID_132324714 A-to-I Human chr3 - 48714461 48714461 48714461 TTGAACCCAGGGGGTGGAGATTGCAGTGAGCCAAAATCACACCACTGCACTCCCGCCTGGGCGAC TTGAACCCAGGGGGTGGAGATTGCAGTGAGCCGAAATCACACCACTGCACTCCCGCCTGGGCGAC T C IP6K2 Ensembl:ENSG00000068745 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7623703 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14859611 RMVar_hsa_circ_82807,RMVar_hsa_circ_217975 29320 RMVar_ID_29320 Human_SNP_ID_132333540 A-to-I Human chr3 - 48749558 48749558 48749558 GAGAATCGCTTGAACCTGGGAGTGGAGGTTGCAGTGAGCCGAGATTGCACCATTGTATTCCACCC GAGAATCGCTTGAACCTGGGAGTGGAGGTTGCGGTGAGCCGAGATTGCACCATTGTATTCCACCC T C PRKAR2A Ensembl:ENSG00000114302 Protein coding intron GSE38233;GSE100210;GSE112787 cultured B-cells;HepG2 cell line;293 Flip-In T-REx cells,empty vector - 24183664,29129909,29967493 RNA-Seq:(High) rs11554283 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26511104 Human_miRNA_ID_621071 RMVar_hsa_circ_217981,RMVar_hsa_circ_76497 29321 RMVar_ID_29321 Human_SNP_ID_132333550 A-to-I Human chr3 - 48749586 48749586 48749586 ATCCCAGCTACTTGAGAGGCTCAGGCAGGAGAATCGCTTGAACCTGGGAGTGGAGGTTGCAGTGA ATCCCAGCTACTTGAGAGGCTCAGGCAGGAGATTCGCTTGAACCTGGGAGTGGAGGTTGCAGTGA T A PRKAR2A Ensembl:ENSG00000114302 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1001057231 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1389221,Human_miRNA_ID_1463362,Human_miRNA_ID_2742012 RMVar_hsa_circ_217981,RMVar_hsa_circ_76497 29322 RMVar_ID_29322 Human_SNP_ID_132333594 A-to-I Human chr3 - 48749753 48749750 48749753 GGCATTGGCCAGGCACGGTGACCCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGG GGCATTGGCCAGGCACGGTGACCCACACCTGT___CCCAGCACTTTGGGAGGCCGAGGCGGGCGG GATT G PRKAR2A Ensembl:ENSG00000114302 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1302429096 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_8210123 Human_miRNA_ID_57612,Human_miRNA_ID_65138,Human_miRNA_ID_564414,Human_miRNA_ID_1589794,Human_miRNA_ID_1686445,Human_miRNA_ID_1941463,Human_miRNA_ID_1944515,Human_miRNA_ID_2085262,Human_miRNA_ID_2115654,Human_miRNA_ID_2199226,Human_miRNA_ID_2202293,Human_miRNA_ID_2314721,Human_miRNA_ID_2317882,Human_miRNA_ID_2321038,Human_miRNA_ID_2324193,Human_miRNA_ID_2327348,Human_miRNA_ID_2518576,Human_miRNA_ID_2521745,Human_miRNA_ID_2773588,Human_miRNA_ID_2814759,Human_miRNA_ID_2820940,Human_miRNA_ID_2827076,Human_miRNA_ID_2830226,Human_miRNA_ID_2834343,Human_miRNA_ID_2839712,Human_miRNA_ID_2844871,Human_miRNA_ID_2847895,Human_miRNA_ID_2862018,Human_miRNA_ID_2889604,Human_miRNA_ID_3111746 RMVar_hsa_circ_217981,RMVar_hsa_circ_76497 29323 RMVar_ID_29323 Human_SNP_ID_132333673 A-to-I Human chr3 - 48750033 48750033 48750033 TTAATTTGTCAGGTGTGGTGATGCATGCATGTAGTCCCAAATACTTAGGAGGCTGAGGTGGAAGG TTAATTTGTCAGGTGTGGTGATGCATGCATGTCGTCCCAAATACTTAGGAGGCTGAGGTGGAAGG T G PRKAR2A Ensembl:ENSG00000114302 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1204701064 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14859884,Human_RBP_ID_23189493,Human_RBP_ID_26510350 RMVar_hsa_circ_217981,RMVar_hsa_circ_76497 29324 RMVar_ID_29324 Human_SNP_ID_132333694 A-to-I Human chr3 - 48750107 48750107 48750107 CGCCCACCTCAGCCTCTCAGAGTGCTGGGATTACAGATGTGAGCCACTGCACCTGGCAAAAAAAA CGCCCACCTCAGCCTCTCAGAGTGCTGGGATTGCAGATGTGAGCCACTGCACCTGGCAAAAAAAA T C PRKAR2A Ensembl:ENSG00000114302 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1250049691 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26508283 RMVar_hsa_circ_217981,RMVar_hsa_circ_76497 29325 RMVar_ID_29325 Human_SNP_ID_132333719 A-to-I Human chr3 - 48750192 48750192 48750192 TGCCGGGCGAATTTTGTATTTTTAATAGAGACAGGGTTTCTCTGTGTTGGTCAGGCTGGTCTCAA TGCCGGGCGAATTTTGTATTTTTAATAGAGACGGGGTTTCTCTGTGTTGGTCAGGCTGGTCTCAA T C PRKAR2A Ensembl:ENSG00000114302 Protein coding intron GSE100210;GSE112787 HepG2 cell line;293 Flip-In T-REx cells,empty vector - 29129909,29967493 RNA-Seq:(High) rs529454014 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_217981,RMVar_hsa_circ_76497 29326 RMVar_ID_29326 Human_SNP_ID_132333720 A-to-I Human chr3 - 48750200 48750200 48750200 CGCCACCATGCCGGGCGAATTTTGTATTTTTAATAGAGACAGGGTTTCTCTGTGTTGGTCAGGCT CGCCACCATGCCGGGCGAATTTTGTATTTTTAGTAGAGACAGGGTTTCTCTGTGTTGGTCAGGCT T C PRKAR2A Ensembl:ENSG00000114302 Protein coding intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs913049410 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4745217 RMVar_hsa_circ_217981,RMVar_hsa_circ_76497 29327 RMVar_ID_29327 Human_SNP_ID_132333738 A-to-I Human chr3 - 48750262 48750262 48750262 GCCTCCCAGATTAAAGTGATTCTCCTGCCTCAACCTCCTGAGTAGCTGGGATTACAGGCATGCGC GCCTCCCAGATTAAAGTGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCATGCGC T C PRKAR2A Ensembl:ENSG00000114302 Protein coding intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs538515963 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_217981,RMVar_hsa_circ_76497 29328 RMVar_ID_29328 Human_SNP_ID_132333739 A-to-I Human chr3 - 48750262 48750262 48750262 GCCTCCCAGATTAAAGTGATTCTCCTGCCTCAACCTCCTGAGTAGCTGGGATTACAGGCATGCGC GCCTCCCAGATTAAAGTGATTCTCCTGCCTCACCCTCCTGAGTAGCTGGGATTACAGGCATGCGC T G PRKAR2A Ensembl:ENSG00000114302 Protein coding intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs538515963 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_217981,RMVar_hsa_circ_76497 29329 RMVar_ID_29329 Human_SNP_ID_132333749 A-to-I Human chr3 - 48750300 48750300 48750300 GGAGTGCAATGGTGCGGTCTTGGCTCACCGCAACCTCCGCCTCCCAGATTAAAGTGATTCTCCTG GGAGTGCAATGGTGCGGTCTTGGCTCACCGCAGCCTCCGCCTCCCAGATTAAAGTGATTCTCCTG T C PRKAR2A Ensembl:ENSG00000114302 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1468794614 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_217981,RMVar_hsa_circ_76497 29330 RMVar_ID_29330 Human_SNP_ID_132333792 A-to-I Human chr3 - 48750476 48750476 48750476 AATTCTCAGGCCAGGCTCAATGGCTCATGCCTATAATTGTAGTGCTTTGGGAGGCTGAGCTGGGA AATTCTCAGGCCAGGCTCAATGGCTCATGCCTGTAATTGTAGTGCTTTGGGAGGCTGAGCTGGGA T C PRKAR2A Ensembl:ENSG00000114302 Protein coding intron GSE38233;GSE100210;GSE112787 cultured B-cells;HepG2 cell line;293 Flip-In T-REx cells,empty vector - 24183664,29129909,29967493 RNA-Seq:(High) rs11554282 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8209714,Human_RBP_ID_22605851,Human_RBP_ID_26508288 Human_miRNA_ID_951404,Human_miRNA_ID_2430216,Human_miRNA_ID_3034783 RMVar_hsa_circ_217981,RMVar_hsa_circ_76497 29331 RMVar_ID_29331 Human_SNP_ID_132333931 A-to-I Human chr3 - 48751183 48751183 48751183 ACAGGGTCTGCAGAAACCTGTTGTATAACTGTAGACACTCTCTAATGGTTCTCAAAGGAGGAAAT ACAGGGTCTGCAGAAACCTGTTGTATAACTGTTGACACTCTCTAATGGTTCTCAAAGGAGGAAAT T A PRKAR2A Ensembl:ENSG00000114302 Protein coding intron GSE100210;GSE112787 HepG2 cell line;293 Flip-In T-REx cells,empty vector - 29129909,29967493 RNA-Seq:(High) rs1443133113 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_603718,Human_RBP_ID_1628113,Human_RBP_ID_1964257,Human_RBP_ID_5206085,Human_RBP_ID_9141350,Human_RBP_ID_14859930,Human_RBP_ID_17291390,Human_RBP_ID_18339234 Human_miRNA_ID_276613,Human_miRNA_ID_1803549,Human_miRNA_ID_2053435,Human_miRNA_ID_2921895,Human_miRNA_ID_2927487 RMVar_hsa_circ_217981,RMVar_hsa_circ_76497 29332 RMVar_ID_29332 Human_SNP_ID_132334835 A-to-I Human chr3 - 48754590 48754590 48754590 TTTTGTACTTTTAGTAGGGACAGGGTTTCCCCATGTTGGCCAGGCTGGTCTGGAACTCCTGACCT TTTTGTACTTTTAGTAGGGACAGGGTTTCCCCGTGTTGGCCAGGCTGGTCTGGAACTCCTGACCT T C PRKAR2A Ensembl:ENSG00000114302 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971075014 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59331,RMVar_hsa_circ_74316,RMVar_hsa_circ_217981,RMVar_hsa_circ_76497,RMVar_hsa_circ_331523,RMVar_hsa_circ_360944,RMVar_hsa_circ_292818,RMVar_hsa_circ_58753,RMVar_hsa_circ_217983,RMVar_hsa_circ_95643,RMVar_hsa_circ_369793,RMVar_hsa_circ_217984,RMVar_hsa_circ_21298,RMVar_hsa_circ_47404,RMVar_hsa_circ_217985,RMVar_hsa_circ_217986 29333 RMVar_ID_29333 Human_SNP_ID_132334844 A-to-I Human chr3 - 48754626 48754626 48754626 GGGACTATAGGCTCCCACCACCAAGCCCAGCTAATTTTTTGTACTTTTAGTAGGGACAGGGTTTC GGGACTATAGGCTCCCACCACCAAGCCCAGCTGATTTTTTGTACTTTTAGTAGGGACAGGGTTTC T C PRKAR2A Ensembl:ENSG00000114302 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041354607 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59331,RMVar_hsa_circ_74316,RMVar_hsa_circ_217981,RMVar_hsa_circ_76497,RMVar_hsa_circ_331523,RMVar_hsa_circ_360944,RMVar_hsa_circ_292818,RMVar_hsa_circ_58753,RMVar_hsa_circ_217983,RMVar_hsa_circ_95643,RMVar_hsa_circ_369793,RMVar_hsa_circ_217984,RMVar_hsa_circ_21298,RMVar_hsa_circ_47404,RMVar_hsa_circ_217985,RMVar_hsa_circ_217986 29334 RMVar_ID_29334 Human_SNP_ID_132354195 A-to-I Human chr3 - 48833174 48833174 48833174 CAATTAGCTGGGTTATGGTGATGTGCACCTGTATTCCCAGCTACTTGGGGGGCTGAGGAAGGAGG CAATTAGCTGGGTTATGGTGATGTGCACCTGTGTTCCCAGCTACTTGGGGGGCTGAGGAAGGAGG T C PRKAR2A Ensembl:ENSG00000114302 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1559649036 Functional Loss SNV dbSNP153 33..33 33 - - - 29335 RMVar_ID_29335 Human_SNP_ID_132376548 A-to-I Human chr3 + 48921634 48921634 48921634 TTTTGTGTTTTTTGTAGCAGTGAGGTTTCACCATGTTGCCCAGGCTTGTTTTGAACTCCTGAGCT TTTTGTGTTTTTTGTAGCAGTGAGGTTTCACCGTGTTGCCCAGGCTTGTTTTGAACTCCTGAGCT A G ARIH2 Ensembl:ENSG00000177479 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1439040246 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14860948 RMVar_hsa_circ_218003,RMVar_hsa_circ_97291,RMVar_hsa_circ_112434,RMVar_hsa_circ_218004 29336 RMVar_ID_29336 Human_SNP_ID_132376959 A-to-I Human chr3 + 48923262 48923262 48923262 TCTATTAAAAATACAAAAAAAATTAGCTGGGCATTGTGGCATGTGCTTGTAATCCCAGCTACTGA TCTATTAAAAATACAAAAAAAATTAGCTGGGCGTTGTGGCATGTGCTTGTAATCCCAGCTACTGA A G ARIH2 Ensembl:ENSG00000177479 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1056364796 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_218003,RMVar_hsa_circ_97291,RMVar_hsa_circ_112434,RMVar_hsa_circ_218004,RMVar_hsa_circ_218006,RMVar_hsa_circ_295895,RMVar_hsa_circ_318926,RMVar_hsa_circ_325999,RMVar_hsa_circ_315810,RMVar_hsa_circ_99714,RMVar_hsa_circ_218005 29337 RMVar_ID_29337 Human_SNP_ID_132377046 A-to-I Human chr3 + 48923539 48923539 48923539 CTTAGATATAGTGAGTGTTTTTTTTTTTTTTTAAGATAGAGTTTCCCTCTTGTTGCCCAGGTTGG CTTAGATATAGTGAGTGTTTTTTTTTTTTTTTTAGATAGAGTTTCCCTCTTGTTGCCCAGGTTGG A T ARIH2 Ensembl:ENSG00000177479 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1240184743 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14861028,Human_RBP_ID_23189505 RMVar_hsa_circ_218003,RMVar_hsa_circ_97291,RMVar_hsa_circ_112434,RMVar_hsa_circ_218004,RMVar_hsa_circ_218006,RMVar_hsa_circ_295895,RMVar_hsa_circ_318926,RMVar_hsa_circ_325999,RMVar_hsa_circ_315810,RMVar_hsa_circ_99714,RMVar_hsa_circ_218005 29338 RMVar_ID_29338 Human_SNP_ID_132377113 A-to-I Human chr3 + 48923764 48923764 48923764 GCTGGCCTTGAACCCCCGACCTTAGGTGATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTAC GCTGGCCTTGAACCCCCGACCTTAGGTGATCCCCCCGCCTCGGCCTCCCAAAGTGCTGGGATTAC A C ARIH2 Ensembl:ENSG00000177479 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904069233 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14861040 RMVar_hsa_circ_218003,RMVar_hsa_circ_97291,RMVar_hsa_circ_112434,RMVar_hsa_circ_218004,RMVar_hsa_circ_218006,RMVar_hsa_circ_295895,RMVar_hsa_circ_318926,RMVar_hsa_circ_325999,RMVar_hsa_circ_315810,RMVar_hsa_circ_99714,RMVar_hsa_circ_218005 29339 RMVar_ID_29339 Human_SNP_ID_132377149 A-to-I Human chr3 + 48923876 48923876 48923876 TGACTGTAGGCTGGGCACAGTGGCTCTTGCCTATAATCCCAGCGTTTTGTAAGGCCAACGCAGGA TGACTGTAGGCTGGGCACAGTGGCTCTTGCCTGTAATCCCAGCGTTTTGTAAGGCCAACGCAGGA A G ARIH2 Ensembl:ENSG00000177479 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1390732538 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_218003,RMVar_hsa_circ_97291,RMVar_hsa_circ_112434,RMVar_hsa_circ_218004,RMVar_hsa_circ_218006,RMVar_hsa_circ_295895,RMVar_hsa_circ_318926,RMVar_hsa_circ_325999,RMVar_hsa_circ_315810,RMVar_hsa_circ_99714,RMVar_hsa_circ_218005 29340 RMVar_ID_29340 Human_SNP_ID_132377150 A-to-I Human chr3 + 48923878 48923878 48923878 ACTGTAGGCTGGGCACAGTGGCTCTTGCCTATAATCCCAGCGTTTTGTAAGGCCAACGCAGGAGG ACTGTAGGCTGGGCACAGTGGCTCTTGCCTATGATCCCAGCGTTTTGTAAGGCCAACGCAGGAGG A G ARIH2 Ensembl:ENSG00000177479 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1352764853 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_218003,RMVar_hsa_circ_97291,RMVar_hsa_circ_112434,RMVar_hsa_circ_218004,RMVar_hsa_circ_218006,RMVar_hsa_circ_295895,RMVar_hsa_circ_318926,RMVar_hsa_circ_325999,RMVar_hsa_circ_315810,RMVar_hsa_circ_99714,RMVar_hsa_circ_218005 29341 RMVar_ID_29341 Human_SNP_ID_132377157 A-to-I Human chr3 + 48923900 48923900 48923900 TCTTGCCTATAATCCCAGCGTTTTGTAAGGCCAACGCAGGAGGATCGCTTGAGGCCAGGAGTTTG TCTTGCCTATAATCCCAGCGTTTTGTAAGGCCGACGCAGGAGGATCGCTTGAGGCCAGGAGTTTG A G ARIH2 Ensembl:ENSG00000177479 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1489782910 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18007099 RMVar_hsa_circ_218003,RMVar_hsa_circ_97291,RMVar_hsa_circ_112434,RMVar_hsa_circ_218004,RMVar_hsa_circ_218006,RMVar_hsa_circ_295895,RMVar_hsa_circ_318926,RMVar_hsa_circ_325999,RMVar_hsa_circ_315810,RMVar_hsa_circ_99714,RMVar_hsa_circ_218005 29342 RMVar_ID_29342 Human_SNP_ID_132377167 A-to-I Human chr3 + 48923952 48923952 48923952 GGCCAGGAGTTTGAAACCAGCCTGAGCAACATAGTAAAACCCTGTTTATACAAAAAATAAAATTA GGCCAGGAGTTTGAAACCAGCCTGAGCAACATGGTAAAACCCTGTTTATACAAAAAATAAAATTA A G ARIH2 Ensembl:ENSG00000177479 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1230434495 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_218003,RMVar_hsa_circ_97291,RMVar_hsa_circ_112434,RMVar_hsa_circ_218004,RMVar_hsa_circ_218006,RMVar_hsa_circ_295895,RMVar_hsa_circ_318926,RMVar_hsa_circ_325999,RMVar_hsa_circ_315810,RMVar_hsa_circ_99714,RMVar_hsa_circ_218005 29343 RMVar_ID_29343 Human_SNP_ID_132377173 A-to-I Human chr3 + 48923984 48923984 48923984 AGTAAAACCCTGTTTATACAAAAAATAAAATTAGGTATGGGGGTGGCATATGCCTGTAGTCCCAG AGTAAAACCCTGTTTATACAAAAAATAAAATTGGGTATGGGGGTGGCATATGCCTGTAGTCCCAG A G ARIH2 Ensembl:ENSG00000177479 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1366746961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14861048,Human_RBP_ID_26685260 RMVar_hsa_circ_218003,RMVar_hsa_circ_97291,RMVar_hsa_circ_112434,RMVar_hsa_circ_218004,RMVar_hsa_circ_218006,RMVar_hsa_circ_295895,RMVar_hsa_circ_318926,RMVar_hsa_circ_325999,RMVar_hsa_circ_315810,RMVar_hsa_circ_99714,RMVar_hsa_circ_218005 29344 RMVar_ID_29344 Human_SNP_ID_132377175 A-to-I Human chr3 + 48924015 48924015 48924015 TAGGTATGGGGGTGGCATATGCCTGTAGTCCCAGTTACTCAGGAGGCTGAGGCAGGAGGATCTGT TAGGTATGGGGGTGGCATATGCCTGTAGTCCCGGTTACTCAGGAGGCTGAGGCAGGAGGATCTGT A G ARIH2 Ensembl:ENSG00000177479 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs562046292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14861049 RMVar_hsa_circ_218003,RMVar_hsa_circ_97291,RMVar_hsa_circ_112434,RMVar_hsa_circ_218004,RMVar_hsa_circ_218006,RMVar_hsa_circ_295895,RMVar_hsa_circ_318926,RMVar_hsa_circ_325999,RMVar_hsa_circ_315810,RMVar_hsa_circ_99714,RMVar_hsa_circ_218005 29345 RMVar_ID_29345 Human_SNP_ID_132377320 A-to-I Human chr3 + 48924544 48924543 48924545 TTATTTATTTGTTTATTTTTTGTGTGTGTGACAGTGTCTCACTCTTGCCCAGGTTGGAGTGCAGT TTATTTATTTGTTTATTTTTTGTGTGTGTGAC__TGTCTCACTCTTGCCCAGGTTGGAGTGCAGT CAG C ARIH2 Ensembl:ENSG00000177479 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270087490 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_3709967,Human_RBP_ID_5506488,Human_RBP_ID_10098195,Human_RBP_ID_14861087,Human_RBP_ID_17574302,Human_RBP_ID_23189511,Human_RBP_ID_24007201 RMVar_hsa_circ_218003,RMVar_hsa_circ_97291,RMVar_hsa_circ_112434,RMVar_hsa_circ_218004,RMVar_hsa_circ_218006,RMVar_hsa_circ_295895,RMVar_hsa_circ_318926,RMVar_hsa_circ_325999,RMVar_hsa_circ_315810,RMVar_hsa_circ_99714,RMVar_hsa_circ_218005 29346 RMVar_ID_29346 Human_SNP_ID_132377387 A-to-I Human chr3 + 48924862 48924862 48924862 GGGATTACAGGTGCATGCCATCATGCCTAGCTAATTTTTGTATTGTTAGTAGAGATGGGGTTTCA GGGATTACAGGTGCATGCCATCATGCCTAGCTGATTTTTGTATTGTTAGTAGAGATGGGGTTTCA A G ARIH2 Ensembl:ENSG00000177479 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1197500858 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15000013,Human_RBP_ID_19115455 RMVar_hsa_circ_218003,RMVar_hsa_circ_97291,RMVar_hsa_circ_112434,RMVar_hsa_circ_218004,RMVar_hsa_circ_89167,RMVar_hsa_circ_218006,RMVar_hsa_circ_295895,RMVar_hsa_circ_318926,RMVar_hsa_circ_325999,RMVar_hsa_circ_315810,RMVar_hsa_circ_99714,RMVar_hsa_circ_218005,RMVar_hsa_circ_218007 29347 RMVar_ID_29347 Human_SNP_ID_132377414 A-to-I Human chr3 + 48924954 48924954 48924954 CTGACCTCGTGATCTGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACTGCG CTGACCTCGTGATCTGCCTGCCTCGGCCTCCCGAAGTGCTGGGATTACAGGTGTGAGCCACTGCG A G ARIH2 Ensembl:ENSG00000177479 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs556236346 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_426557 RMVar_hsa_circ_218003,RMVar_hsa_circ_97291,RMVar_hsa_circ_112434,RMVar_hsa_circ_218004,RMVar_hsa_circ_89167,RMVar_hsa_circ_218006,RMVar_hsa_circ_295895,RMVar_hsa_circ_318926,RMVar_hsa_circ_325999,RMVar_hsa_circ_315810,RMVar_hsa_circ_99714,RMVar_hsa_circ_218005,RMVar_hsa_circ_218007 29348 RMVar_ID_29348 Human_SNP_ID_132380362 A-to-I Human chr3 + 48936881 48936881 48936881 AAACCCTGTCTGTACTAAAAGTACAAAAAATTAGCCGGGCATGGTGGCAGGCGCCTATAGTCCCA AAACCCTGTCTGTACTAAAAGTACAAAAAATTGGCCGGGCATGGTGGCAGGCGCCTATAGTCCCA A G ARIH2 Ensembl:ENSG00000177479 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1045165159 Functional Loss SNV dbSNP153 33..33 33 - - - 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 29349 RMVar_ID_29349 Human_SNP_ID_132380588 A-to-I Human chr3 + 48937836 48937836 48937836 TTGGGAGGCCAGGGCGGGTGGATCATGAGATCAGGAGATCAAGATCATCCTGGCCAACACAATGA TTGGGAGGCCAGGGCGGGTGGATCATGAGATCGGGAGATCAAGATCATCCTGGCCAACACAATGA A G ARIH2 Ensembl:ENSG00000177479 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs568086156 Functional Loss SNV dbSNP153 33..33 33 - - - 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 29350 RMVar_ID_29350 Human_SNP_ID_132380597 A-to-I Human chr3 + 48937864 48937864 48937864 GATCAGGAGATCAAGATCATCCTGGCCAACACAATGAAACGCCGTCTCTACTAAAAATACAAAAA GATCAGGAGATCAAGATCATCCTGGCCAACACGATGAAACGCCGTCTCTACTAAAAATACAAAAA A G ARIH2 Ensembl:ENSG00000177479 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1182733550 Functional Loss SNV dbSNP153 33..33 33 - - - 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 29351 RMVar_ID_29351 Human_SNP_ID_132380916 A-to-I Human chr3 + 48938992 48938991 48938993 GAAACCCATTTATTTATTTAATTTTTTGAGACAGAGTGTTGCTCGTCCCCCAGGCTGGAGTGCAG GAAACCCATTTATTTATTTAATTTTTTGAGAC__AGTGTTGCTCGTCCCCCAGGCTGGAGTGCAG CAG C ARIH2 Ensembl:ENSG00000177479 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251443346 Functional Loss DEL dbSNP153 33..34 33 - - - 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 29352 RMVar_ID_29352 Human_SNP_ID_132381955 A-to-I Human chr3 + 48941980 48941980 48941980 TGATCTTGGCACACTGCACCCTCCGCCCCCCGAGTTCAGGTGACTCTTCTGCCTCAGCCTCCCGA TGATCTTGGCACACTGCACCCTCCGCCCCCCGGGTTCAGGTGACTCTTCTGCCTCAGCCTCCCGA A G ARIH2 Ensembl:ENSG00000177479 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1210087913 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14861777 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 29353 RMVar_ID_29353 Human_SNP_ID_132389638 A-to-I Human chr3 + 48972576 48972576 48972576 TGAGGCAGGAAAATCACTTGAACCAGGGAGGCAGAGGCTGCAGTGAGCCAAGATCATGCCATTGC TGAGGCAGGAAAATCACTTGAACCAGGGAGGCGGAGGCTGCAGTGAGCCAAGATCATGCCATTGC A G ARIH2 Ensembl:ENSG00000177479 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs865849897 Functional Loss SNV dbSNP153 33..33 33 - - - 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_8152,RMVar_hsa_circ_43608,RMVar_hsa_circ_109511,RMVar_hsa_circ_317610,RMVar_hsa_circ_358963,RMVar_hsa_circ_218012 29354 RMVar_ID_29354 Human_SNP_ID_132389785 A-to-I Human chr3 + 48973194 48973194 48973194 GGCCGGGCACAGTGGCCCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGCAGATCTCG GGCCGGGCACAGTGGCCCACGCCTGTAATCCCGGCACTTTGGGAGGCTGAGGCGGGCAGATCTCG A G ARIH2 Ensembl:ENSG00000177479 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1397701035 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17574084 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_8152,RMVar_hsa_circ_43608,RMVar_hsa_circ_109511,RMVar_hsa_circ_317610,RMVar_hsa_circ_358963,RMVar_hsa_circ_218012 29355 RMVar_ID_29355 Human_SNP_ID_132390542 A-to-I Human chr3 + 48976192 48976192 48976192 CCTTGGCCTCTTAAAGTGCTGGGATTATAGGCATGAGCCACCGAGCCTGTACTTTTTTTTTTTTT CCTTGGCCTCTTAAAGTGCTGGGATTATAGGCGTGAGCCACCGAGCCTGTACTTTTTTTTTTTTT A G ARIH2 Ensembl:ENSG00000177479 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1213747191 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89167,RMVar_hsa_circ_320782,RMVar_hsa_circ_367702,RMVar_hsa_circ_218007,RMVar_hsa_circ_8152,RMVar_hsa_circ_43608,RMVar_hsa_circ_317610,RMVar_hsa_circ_358963,RMVar_hsa_circ_299424,RMVar_hsa_circ_218014 29356 RMVar_ID_29356 Human_SNP_ID_132390577 A-to-I Human chr3 + 48976300 48976300 48976300 CAATGGTGTGATCTTGGCTCAATGCAACATCTACCTCCTGGGTTCAAGCGATTCTCACTCCGCCT CAATGGTGTGATCTTGGCTCAATGCAACATCTGCCTCCTGGGTTCAAGCGATTCTCACTCCGCCT A G ARIH2 Ensembl:ENSG00000177479 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1367843549 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89167,RMVar_hsa_circ_320782,RMVar_hsa_circ_367702,RMVar_hsa_circ_218007,RMVar_hsa_circ_8152,RMVar_hsa_circ_43608,RMVar_hsa_circ_317610,RMVar_hsa_circ_358963,RMVar_hsa_circ_299424,RMVar_hsa_circ_218014 29357 RMVar_ID_29357 Human_SNP_ID_132391289 A-to-I Human chr3 + 48978579 48978579 48978579 GACCTCAGGTGATCCATCCGCCTTGGCCTCCCAGAGTGCTGGTATTACAGGTGTGAGCTACCGCA GACCTCAGGTGATCCATCCGCCTTGGCCTCCCGGAGTGCTGGTATTACAGGTGTGAGCTACCGCA A G ARIH2 Ensembl:ENSG00000177479 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1315274590 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24007513 RMVar_hsa_circ_89167,RMVar_hsa_circ_320782,RMVar_hsa_circ_367702,RMVar_hsa_circ_218007,RMVar_hsa_circ_8152,RMVar_hsa_circ_43608,RMVar_hsa_circ_317610,RMVar_hsa_circ_358963,RMVar_hsa_circ_299424,RMVar_hsa_circ_218014 29358 RMVar_ID_29358 Human_SNP_ID_132391314 A-to-I Human chr3 + 48978688 48978688 48978688 GGTTTTATAGAAATGTGTTATTTGCCAGGCGCAGTGGCTCACGCCTATAATCCCAGCACTTTGAG GGTTTTATAGAAATGTGTTATTTGCCAGGCGCGGTGGCTCACGCCTATAATCCCAGCACTTTGAG A G ARIH2 Ensembl:ENSG00000177479 Protein coding intron GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs1414288523 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17573644 RMVar_hsa_circ_89167,RMVar_hsa_circ_320782,RMVar_hsa_circ_367702,RMVar_hsa_circ_218007,RMVar_hsa_circ_8152,RMVar_hsa_circ_43608,RMVar_hsa_circ_317610,RMVar_hsa_circ_358963,RMVar_hsa_circ_299424,RMVar_hsa_circ_218014 29359 RMVar_ID_29359 Human_SNP_ID_132393085 A-to-I Human chr3 - 48986390 48986390 48986390 CCCAGGAGTGGAGGCCGCAGTGAGCAGAGATCATGCCACTGTACTCCAGTCTGGGCGATAGAGCG CCCAGGAGTGGAGGCCGCAGTGAGCAGAGATCTTGCCACTGTACTCCAGTCTGGGCGATAGAGCG T A AC137630.1 Ensembl:ENSG00000223343 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1274723378 Functional Loss SNV dbSNP153 33..33 33 - - - 29360 RMVar_ID_29360 Human_SNP_ID_132398777 A-to-I Human chr3 + 49009134 49009134 49009134 AAACTCCTGACCTCAAGTGATTCGCCTGCCTCAGCCCCCCAAATTGCTGGAATTATAGGCATGAG AAACTCCTGACCTCAAGTGATTCGCCTGCCTCCGCCCCCCAAATTGCTGGAATTATAGGCATGAG A C WDR6 Ensembl:ENSG00000178252 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1191621408 Functional Loss SNV dbSNP153 33..33 33 - - - 29361 RMVar_ID_29361 Human_SNP_ID_132399009 A-to-I Human chr3 + 49009867 49009867 49009867 CTCTCACCTCAGCCTCCCAAGTAGCTGGGACTACAGGCATGCGCCATTATGCCCAGCTCATTTGT CTCTCACCTCAGCCTCCCAAGTAGCTGGGACTGCAGGCATGCGCCATTATGCCCAGCTCATTTGT A G WDR6 Ensembl:ENSG00000178252 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1054675602 Functional Loss SNV dbSNP153 33..33 33 - - - 29362 RMVar_ID_29362 Human_SNP_ID_132399118 A-to-I Human chr3 + 49010295 49010295 49010295 GGGCATGGTGGCGGATGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGGATGGCGTAAA GGGCATGGTGGCGGATGCCTGTAGTCCCAGCTCCTTGGGAGGCTGAGGCAGGAGGATGGCGTAAA A C WDR6 Ensembl:ENSG00000178252 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1421583709 Functional Loss SNV dbSNP153 33..33 33 - - - 29363 RMVar_ID_29363 Human_SNP_ID_132399129 A-to-I Human chr3 + 49010355 49010355 49010355 GTAAACCTGGGAGGCAGAGCTTGTAGTGAGCCAAGATCGCGCCACAGCACTCCAGCTTGGGCGGC GTAAACCTGGGAGGCAGAGCTTGTAGTGAGCCCAGATCGCGCCACAGCACTCCAGCTTGGGCGGC A C WDR6 Ensembl:ENSG00000178252 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1205801648 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10098345 29364 RMVar_ID_29364 Human_SNP_ID_132399141 A-to-I Human chr3 + 49010396 49010396 49010396 CCACAGCACTCCAGCTTGGGCGGCAGAGTGAGACTTTGTCTCAAAAAAAAAAAAGAGTGACTGAT CCACAGCACTCCAGCTTGGGCGGCAGAGTGAGGCTTTGTCTCAAAAAAAAAAAAGAGTGACTGAT A G WDR6 Ensembl:ENSG00000178252 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1401942695 Functional Loss SNV dbSNP153 33..33 33 - - - 29365 RMVar_ID_29365 Human_SNP_ID_132399180 A-to-I Human chr3 + 49010529 49010529 49010529 CCGCAGGTCAGGAGTTCGAGACCAGCGTGGCCAACATGGTGAAACCCTGTCTCTACTAAAAATAT CCGCAGGTCAGGAGTTCGAGACCAGCGTGGCCCACATGGTGAAACCCTGTCTCTACTAAAAATAT A C WDR6 Ensembl:ENSG00000178252 Protein coding intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1027747699 Functional Loss SNV dbSNP153 33..33 33 - - - 29366 RMVar_ID_29366 Human_SNP_ID_132399380 A-to-I Human chr3 + 49011258 49011258 49011258 AGGCACGTGCCACCACACCTGGCTAATTTTTTAGTAGAGATGGGGTTTTCACCTTGTTGGCCAGG AGGCACGTGCCACCACACCTGGCTAATTTTTTCGTAGAGATGGGGTTTTCACCTTGTTGGCCAGG A C WDR6 Ensembl:ENSG00000178252 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1411914394 Functional Loss SNV dbSNP153 33..33 33 - - - 29367 RMVar_ID_29367 Human_SNP_ID_132399381 A-to-I Human chr3 + 49011258 49011258 49011258 AGGCACGTGCCACCACACCTGGCTAATTTTTTAGTAGAGATGGGGTTTTCACCTTGTTGGCCAGG AGGCACGTGCCACCACACCTGGCTAATTTTTTGGTAGAGATGGGGTTTTCACCTTGTTGGCCAGG A G WDR6 Ensembl:ENSG00000178252 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1411914394 Functional Loss SNV dbSNP153 33..33 33 - - - 29368 RMVar_ID_29368 Human_SNP_ID_132399389 A-to-I Human chr3 + 49011293 49011293 49011293 AGAGATGGGGTTTTCACCTTGTTGGCCAGGCTAGTCCTGAACCCCTGACCTCAGGTGATTCATCC AGAGATGGGGTTTTCACCTTGTTGGCCAGGCTGGTCCTGAACCCCTGACCTCAGGTGATTCATCC A G WDR6 Ensembl:ENSG00000178252 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1036433148 Functional Loss SNV dbSNP153 33..33 33 - - - 29369 RMVar_ID_29369 Human_SNP_ID_132404645 A-to-I Human chr3 - 49024961 49024961 49024961 TACTTCTTTTCCGATGGGATCCGGCTAAAGAAATATCGCGGTATGGGTTCTCTCGATGCCATGGA TACTTCTTTTCCGATGGGATCCGGCTAAAGAAGTATCGCGGTATGGGTTCTCTCGATGCCATGGA T C IMPDH2 Ensembl:ENSG00000178035 Protein coding exon GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs561152714 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_69234,Human_RBP_ID_604009,Human_RBP_ID_1964476,Human_RBP_ID_3710146,Human_RBP_ID_5474360,Human_RBP_ID_8873011,Human_RBP_ID_9141415,Human_RBP_ID_9354394,Human_RBP_ID_17661396,Human_RBP_ID_18007189,Human_RBP_ID_18446710,Human_RBP_ID_18810262,Human_RBP_ID_22455430,Human_RBP_ID_22824077,Human_RBP_ID_27719269 Human_Splice_Rec_427117,Human_Splice_Rec_427122,Human_Splice_Rec_427123,Human_Splice_Rec_427142,Human_Splice_Rec_427143,Human_Splice_Rec_427168,Human_Splice_Rec_427169,Human_Splice_Rec_427178,Human_Splice_Rec_427179,Human_Splice_Rec_427184 Human_miRNA_ID_2363530,Human_miRNA_ID_2927489 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_58687,RMVar_hsa_circ_300468 29370 RMVar_ID_29370 Human_SNP_ID_132405339 A-to-I Human chr3 - 49027045 49027027 49027046 GCCCTTCTTCACATCTCACCTCCCACGTAGATAATGACAAAGAGGGAAGACTTGGTGGTAGCCCC GCCCTTCTTCACATCTCACCTCCCACGTAGA___________________CTTGGTGGTAGCCCC GTCTTCCCTCTTTGTCATTA G IMPDH2 Ensembl:ENSG00000178035 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1254751586 Functional Loss DEL dbSNP153 32..50 33 - - - Human_RBP_ID_69239,Human_RBP_ID_2789012,Human_RBP_ID_3963999,Human_RBP_ID_18012811,Human_RBP_ID_22091690 Human_Splice_Rec_427130,Human_Splice_Rec_427131,Human_Splice_Rec_427158,Human_Splice_Rec_427159,Human_Splice_Rec_427186,Human_Splice_Rec_427187,Human_Splice_Rec_427200,Human_Splice_Rec_427201,Human_Splice_Rec_427206 Human_miRNA_ID_2955140 RMVar_hsa_circ_93264,RMVar_hsa_circ_115625,RMVar_hsa_circ_102260,RMVar_hsa_circ_2113,RMVar_hsa_circ_3755,RMVar_hsa_circ_218034,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_26823,RMVar_hsa_circ_76880,RMVar_hsa_circ_218041,RMVar_hsa_circ_218042,RMVar_hsa_circ_99332,RMVar_hsa_circ_218043,RMVar_hsa_circ_218044,RMVar_hsa_circ_218045,RMVar_hsa_circ_369713 29371 RMVar_ID_29371 Human_SNP_ID_132405539 A-to-I Human chr3 - 49027713 49027713 49027713 CTCAAAGAGGAGGAACATGACTGTTTCTTGGAAGAGGTGGGTGCCACTGGCAGAGTAGATCCAAG CTCAAAGAGGAGGAACATGACTGTTTCTTGGACGAGGTGGGTGCCACTGGCAGAGTAGATCCAAG T G IMPDH2 Ensembl:ENSG00000178035 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1458568504 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1628404,Human_RBP_ID_18012812,Human_RBP_ID_22091691,Human_RBP_ID_22824092,Human_RBP_ID_24007680 Human_Splice_Rec_427129,Human_Splice_Rec_427157,Human_Splice_Rec_427185,Human_Splice_Rec_427199,Human_Splice_Rec_427205 RMVar_hsa_circ_115625,RMVar_hsa_circ_102260,RMVar_hsa_circ_2113,RMVar_hsa_circ_3755,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_76880,RMVar_hsa_circ_218041,RMVar_hsa_circ_218042,RMVar_hsa_circ_99332,RMVar_hsa_circ_218043,RMVar_hsa_circ_218044,RMVar_hsa_circ_218045,RMVar_hsa_circ_369713 29372 RMVar_ID_29372 Human_SNP_ID_132407626 A-to-I Human chr3 - 49033865 49033865 49033865 CTCCTGTCTCAGCCTCCCGATTAGCTGGGACTACAGGAGCCCGCCACCACACCCGGCTATTTTTT CTCCTGTCTCAGCCTCCCGATTAGCTGGGACTGCAGGAGCCCGCCACCACACCCGGCTATTTTTT T C QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs989875428 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54028,RMVar_hsa_circ_106948,RMVar_hsa_circ_218050 29373 RMVar_ID_29373 Human_SNP_ID_132407627 A-to-I Human chr3 - 49033865 49033865 49033865 CTCCTGTCTCAGCCTCCCGATTAGCTGGGACTACAGGAGCCCGCCACCACACCCGGCTATTTTTT CTCCTGTCTCAGCCTCCCGATTAGCTGGGACTCCAGGAGCCCGCCACCACACCCGGCTATTTTTT T G QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs989875428 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54028,RMVar_hsa_circ_106948,RMVar_hsa_circ_218050 29374 RMVar_ID_29374 Human_SNP_ID_132407806 A-to-I Human chr3 - 49034330 49034330 49034330 CCAAGGAATCCTCCCACCTCAGCCTCCCTGGTAGCTGGGATCACAGATGTGCACCATCACACGAC CCAAGGAATCCTCCCACCTCAGCCTCCCTGGTCGCTGGGATCACAGATGTGCACCATCACACGAC T G QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1046490309 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25741820 RMVar_hsa_circ_54028,RMVar_hsa_circ_106948,RMVar_hsa_circ_218050 29375 RMVar_ID_29375 Human_SNP_ID_132407857 A-to-I Human chr3 - 49034540 49034540 49034540 CAGGAAACTGGCAGGAGGAGTCTTTGAGTCCAAGAGCTCAAGGCTGCAGTTAGCCATGATTGTGT CAGGAAACTGGCAGGAGGAGTCTTTGAGTCCAGGAGCTCAAGGCTGCAGTTAGCCATGATTGTGT T C QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1375094921 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54028,RMVar_hsa_circ_106948,RMVar_hsa_circ_218050 29376 RMVar_ID_29376 Human_SNP_ID_132408024 A-to-I Human chr3 - 49035235 49035235 49035235 AGACCTCATCTCCACTAAAAATCAAAAAAAATAATCGAGTGTGATGGTGCACACCTGTGATCCCA AGACCTCATCTCCACTAAAAATCAAAAAAAATGATCGAGTGTGATGGTGCACACCTGTGATCCCA T C QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215454302 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54028,RMVar_hsa_circ_106948,RMVar_hsa_circ_218050 29377 RMVar_ID_29377 Human_SNP_ID_132408038 A-to-I Human chr3 - 49035298 49035298 49035298 GTAGGCCGAGGTAGGAGAATTGCTTCAGCCCAAGATTTGAAGACCAGCCTGGGCAACATAGCAAG GTAGGCCGAGGTAGGAGAATTGCTTCAGCCCAGGATTTGAAGACCAGCCTGGGCAACATAGCAAG T C QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs367696127 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54028,RMVar_hsa_circ_106948,RMVar_hsa_circ_218050 29378 RMVar_ID_29378 Human_SNP_ID_132408168 A-to-I Human chr3 - 49035864 49035864 49035864 TGCCATGTTGTCTAGGCTGGTCTCAAACTCCTAGGTTCCAGTGATCCACCTGCCTTGGCCTCCCA TGCCATGTTGTCTAGGCTGGTCTCAAACTCCTGGGTTCCAGTGATCCACCTGCCTTGGCCTCCCA T C QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1321449864 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54028,RMVar_hsa_circ_106948,RMVar_hsa_circ_218050 29379 RMVar_ID_29379 Human_SNP_ID_132408612 A-to-I Human chr3 - 49037481 49037481 49037481 GCAATCCACCTGCCTCAGCCTCCCAAAGTGCTAGGTTACAGGTGTGAGCCACCTTGCCTGGCCTT GCAATCCACCTGCCTCAGCCTCCCAAAGTGCTGGGTTACAGGTGTGAGCCACCTTGCCTGGCCTT T C QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1047446537 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54028,RMVar_hsa_circ_106948,RMVar_hsa_circ_218050 29380 RMVar_ID_29380 Human_SNP_ID_132408637 A-to-I Human chr3 - 49037569 49037569 49037569 TGCCACCACACCCAGCTAATTTTTGTATTTTCAGTTGATACGGGGTTTCACCATGTTGGCCGCGC TGCCACCACACCCAGCTAATTTTTGTATTTTCGGTTGATACGGGGTTTCACCATGTTGGCCGCGC T C QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1365285541 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54028,RMVar_hsa_circ_106948,RMVar_hsa_circ_218050 29381 RMVar_ID_29381 Human_SNP_ID_132408669 A-to-I Human chr3 - 49037685 49037685 49037685 CTCTCTTGCCCACGTTGGAGTTCAGTGGTGCAATCTCGGCTCACTGTAACCTCCACCTCCTGGGT CTCTCTTGCCCACGTTGGAGTTCAGTGGTGCAGTCTCGGCTCACTGTAACCTCCACCTCCTGGGT T C QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs976332017 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1205758 RMVar_hsa_circ_54028,RMVar_hsa_circ_106948,RMVar_hsa_circ_218050 29382 RMVar_ID_29382 Human_SNP_ID_132408996 A-to-I Human chr3 - 49038791 49038791 49038791 AACCTCTAACCTCAGGTGATCCACCTGCCTCAACCTCCCAAAGTGCTAGGATTACAGGCGTGAAC AACCTCTAACCTCAGGTGATCCACCTGCCTCAGCCTCCCAAAGTGCTAGGATTACAGGCGTGAAC T C QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1036858283 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54028,RMVar_hsa_circ_106948,RMVar_hsa_circ_218050 29383 RMVar_ID_29383 Human_SNP_ID_132409010 A-to-I Human chr3 - 49038861 49038861 49038861 TGCCACACCCGGATAATTTTTTGTATTTTAGTAGAGACGAGGTTTCACTGTGTTGCCTAGGCTTG TGCCACACCCGGATAATTTTTTGTATTTTAGTGGAGACGAGGTTTCACTGTGTTGCCTAGGCTTG T C QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1321088410 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17573646 RMVar_hsa_circ_54028,RMVar_hsa_circ_106948,RMVar_hsa_circ_218050 29384 RMVar_ID_29384 Human_SNP_ID_132409025 A-to-I Human chr3 - 49038944 49038943 49038944 TGGCTCACTGCAACCTCTGGCTCCTGGATTCAAGCAGTTCTTCTGCCTCAGCCTCCCAAGTAGCT TGGCTCACTGCAACCTCTGGCTCCTGGATTCA_GCAGTTCTTCTGCCTCAGCCTCCCAAGTAGCT CT C QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1264812551 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_14863970 RMVar_hsa_circ_54028,RMVar_hsa_circ_106948,RMVar_hsa_circ_218050 29385 RMVar_ID_29385 Human_SNP_ID_132409026 A-to-I Human chr3 - 49038944 49038944 49038944 TGGCTCACTGCAACCTCTGGCTCCTGGATTCAAGCAGTTCTTCTGCCTCAGCCTCCCAAGTAGCT TGGCTCACTGCAACCTCTGGCTCCTGGATTCATGCAGTTCTTCTGCCTCAGCCTCCCAAGTAGCT T A QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs956184026 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14863970 RMVar_hsa_circ_54028,RMVar_hsa_circ_106948,RMVar_hsa_circ_218050 29386 RMVar_ID_29386 Human_SNP_ID_132409458 A-to-I Human chr3 - 49040423 49040423 49040423 CTCCTTTTTTGTGGAGAGCAAGGTCTTGCTGTATTGCCCAGGCAGGTCTCCAACTCCTGGGCTCC CTCCTTTTTTGTGGAGAGCAAGGTCTTGCTGTGTTGCCCAGGCAGGTCTCCAACTCCTGGGCTCC T C QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909181065 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14864016,Human_RBP_ID_25741861 RMVar_hsa_circ_54028,RMVar_hsa_circ_106948,RMVar_hsa_circ_218050 29387 RMVar_ID_29387 Human_SNP_ID_132411556 A-to-I Human chr3 - 49048218 49048218 49048218 TGAGGCAGGAGAATAGCTTGAACCCGGGAGACAGAGGTTGAGGTGAGCCGAGATCCTGCCATTGC TGAGGCAGGAGAATAGCTTGAACCCGGGAGACTGAGGTTGAGGTGAGCCGAGATCCTGCCATTGC T A QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1439379843 Functional Loss SNV dbSNP153 33..33 33 - - - 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 29388 RMVar_ID_29388 Human_SNP_ID_132411557 A-to-I Human chr3 - 49048218 49048218 49048218 TGAGGCAGGAGAATAGCTTGAACCCGGGAGACAGAGGTTGAGGTGAGCCGAGATCCTGCCATTGC TGAGGCAGGAGAATAGCTTGAACCCGGGAGACGGAGGTTGAGGTGAGCCGAGATCCTGCCATTGC T C QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1439379843 Functional Loss SNV dbSNP153 33..33 33 - - - 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 29389 RMVar_ID_29389 Human_SNP_ID_132411685 A-to-I Human chr3 - 49048599 49048599 49048599 GTATTTTAGTAGAGATGGGGTTTCACCGTGTTAGCCAGGATGGTCTCAGTCTCTTGACCTCGTGA GTATTTTAGTAGAGATGGGGTTTCACCGTGTTGGCCAGGATGGTCTCAGTCTCTTGACCTCGTGA T C QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs914593825 Functional Loss SNV dbSNP153 33..33 33 - - - 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 29390 RMVar_ID_29390 Human_SNP_ID_132411840 A-to-I Human chr3 - 49049039 49049039 49049039 AAATTAGTTGGGCATGGTGGTGCATATCTGTAATCCTAGCTACTCGGGAGGCTGAGAAAGGAGAA AAATTAGTTGGGCATGGTGGTGCATATCTGTAGTCCTAGCTACTCGGGAGGCTGAGAAAGGAGAA T C QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1292351246 Functional Loss SNV dbSNP153 33..33 33 - - - 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 29391 RMVar_ID_29391 Human_SNP_ID_132411931 A-to-I Human chr3 - 49049393 49049393 49049393 TCACCCAGGCTGGAGTGCAGTGGCACTGTCTCAGCTCACTGTAACCTCCGTCTCCTGGGTTCAAG TCACCCAGGCTGGAGTGCAGTGGCACTGTCTCGGCTCACTGTAACCTCCGTCTCCTGGGTTCAAG T C QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs56030853 Functional Loss SNV dbSNP153 33..33 33 - - - 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 29392 RMVar_ID_29392 Human_SNP_ID_132415822 A-to-I Human chr3 - 49062587 49062587 49062587 GGAGGCCAAGGCAGGTGGATCACTTGAGGTTAAGAGTTTGAGACCAGCCTGGCTAACATGGTGAA GGAGGCCAAGGCAGGTGGATCACTTGAGGTTAGGAGTTTGAGACCAGCCTGGCTAACATGGTGAA T C QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs56063217 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 29393 RMVar_ID_29393 Human_SNP_ID_132416394 A-to-I Human chr3 - 49064499 49064499 49064499 CCTGTAATCTCAGCACTTTGGGAGGATGCGGTAGGTGGATTGCTTGAGGATATGAGTTCAAGACC CCTGTAATCTCAGCACTTTGGGAGGATGCGGTGGGTGGATTGCTTGAGGATATGAGTTCAAGACC T C QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs903493855 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 29394 RMVar_ID_29394 Human_SNP_ID_132416511 A-to-I Human chr3 - 49064895 49064895 49064895 CTCCTGTCTCAGCCTCCTGATTAGCTGGGATTACAGGCATGCACCACCACACCTGGCTAGTTTTT CTCCTGTCTCAGCCTCCTGATTAGCTGGGATTGCAGGCATGCACCACCACACCTGGCTAGTTTTT T C QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1302018919 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 29395 RMVar_ID_29395 Human_SNP_ID_132416512 A-to-I Human chr3 - 49064905 49064905 49064905 TCAGGCTGTTCTCCTGTCTCAGCCTCCTGATTAGCTGGGATTACAGGCATGCACCACCACACCTG TCAGGCTGTTCTCCTGTCTCAGCCTCCTGATTGGCTGGGATTACAGGCATGCACCACCACACCTG T C QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1410002862 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 29396 RMVar_ID_29396 Human_SNP_ID_132416625 A-to-I Human chr3 - 49065341 49065341 49065341 CAGGCGTTCGAGAACAGCCTGGCCAACATGGCAAAAACCTGTCTCTACTAAAAATACAAAAATTA CAGGCGTTCGAGAACAGCCTGGCCAACATGGCGAAAACCTGTCTCTACTAAAAATACAAAAATTA T C QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs945206275 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 29397 RMVar_ID_29397 Human_SNP_ID_132416824 A-to-I Human chr3 - 49065982 49065982 49065982 CCATTCCTGGCCAGAAGTGATTCACAAATGGTAGTTCAAGAGACTCGTAGGGGCCTGTAATCCCA CCATTCCTGGCCAGAAGTGATTCACAAATGGTGGTTCAAGAGACTCGTAGGGGCCTGTAATCCCA T C QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1399574050 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 29398 RMVar_ID_29398 Human_SNP_ID_132417083 A-to-I Human chr3 - 49066962 49066962 49066962 ATGTTCTCGGCTCACTGCAACCTCCGCCCCCCAGGTTCAAGCTATTGTCCTACCTCAGCCTCCTG ATGTTCTCGGCTCACTGCAACCTCCGCCCCCCGGGTTCAAGCTATTGTCCTACCTCAGCCTCCTG T C QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs770826319 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 29399 RMVar_ID_29399 Human_SNP_ID_132417449 A-to-I Human chr3 - 49068235 49068235 49068235 CTGCCATTTCAGCCTCTGGAGTGGCTGGGACTACAGGCATGCACCACCACGCCTGGCTAATATTT CTGCCATTTCAGCCTCTGGAGTGGCTGGGACTGCAGGCATGCACCACCACGCCTGGCTAATATTT T C QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs911767477 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 29400 RMVar_ID_29400 Human_SNP_ID_132417988 A-to-I Human chr3 - 49069759 49069759 49069759 GTAAGAATCATAGGCTGGGTGCAGTGGCTCATACCTGTAATCTCAGTACTTTGGGAGGCTGAGGC GTAAGAATCATAGGCTGGGTGCAGTGGCTCATGCCTGTAATCTCAGTACTTTGGGAGGCTGAGGC T C QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs897764277 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 29401 RMVar_ID_29401 Human_SNP_ID_132418093 A-to-I Human chr3 - 49070154 49070154 49070154 CAGGTGCCTATAGTCCCAGCTATTCGGAGGCTAAGGCAGGAGAATTGCTTGAACCTGGGAAGCCA CAGGTGCCTATAGTCCCAGCTATTCGGAGGCTGAGGCAGGAGAATTGCTTGAACCTGGGAAGCCA T C QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1288122671 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 29402 RMVar_ID_29402 Human_SNP_ID_132418294 A-to-I Human chr3 - 49070965 49070965 49070965 GGAAGGTAGAGGTTGCAGTGAATCAAGATCACACCACTGCACCACAGCCTGGGTGACAGAGCAGA GGAAGGTAGAGGTTGCAGTGAATCAAGATCACGCCACTGCACCACAGCCTGGGTGACAGAGCAGA T C QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348576076 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247964 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 29403 RMVar_ID_29403 Human_SNP_ID_132418584 A-to-I Human chr3 - 49072086 49072086 49072086 CTTTAAGTGATCTGCCAACCTCGGCCTCCCAAAGTGCTGGGATTGTAGGCATGAGCCACCACGCC CTTTAAGTGATCTGCCAACCTCGGCCTCCCAAGGTGCTGGGATTGTAGGCATGAGCCACCACGCC T C QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs138811620 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 29404 RMVar_ID_29404 Human_SNP_ID_132418664 A-to-I Human chr3 - 49072404 49072404 49072404 CTCCCACCTCAGCCTCCCGAGTACATGGGACCACAGGCGCACACCACCAACACCTGCCTAATTTT CTCCCACCTCAGCCTCCCGAGTACATGGGACCGCAGGCGCACACCACCAACACCTGCCTAATTTT T C QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs942436536 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3710194 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 29405 RMVar_ID_29405 Human_SNP_ID_132418665 A-to-I Human chr3 - 49072404 49072404 49072404 CTCCCACCTCAGCCTCCCGAGTACATGGGACCACAGGCGCACACCACCAACACCTGCCTAATTTT CTCCCACCTCAGCCTCCCGAGTACATGGGACCCCAGGCGCACACCACCAACACCTGCCTAATTTT T G QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs942436536 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3710194 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 29406 RMVar_ID_29406 Human_SNP_ID_132418801 A-to-I Human chr3 - 49072942 49072942 49072942 TACCTCCTGGGCTCAGGTGATGCTCTCACCTCAGCCTCCCGAGTAGCTAGGACTACAGGTGCGTG TACCTCCTGGGCTCAGGTGATGCTCTCACCTCCGCCTCCCGAGTAGCTAGGACTACAGGTGCGTG T G QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1158683738 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 29407 RMVar_ID_29407 Human_SNP_ID_132419409 A-to-I Human chr3 - 49075228 49075228 49075228 ACCTCCAAGGCTTAAGCGATCATCCAGCCTCAACCTCCAAGTAGCTGGGACCACAGGCATGTACC ACCTCCAAGGCTTAAGCGATCATCCAGCCTCAGCCTCCAAGTAGCTGGGACCACAGGCATGTACC T C QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978901062 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 29408 RMVar_ID_29408 Human_SNP_ID_132419513 A-to-I Human chr3 - 49075592 49075592 49075592 AGTTTCGCTCTTGTTGTCCAGGCTAGAATGCAATGGAGCCATCTCGGCTCACTGCAACCTGCACC AGTTTCGCTCTTGTTGTCCAGGCTAGAATGCAGTGGAGCCATCTCGGCTCACTGCAACCTGCACC T C QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs140519943 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7204420,Human_RBP_ID_14864549 Clinvar_Rec_98 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 29409 RMVar_ID_29409 Human_SNP_ID_132420452 A-to-I Human chr3 - 49079078 49079078 49079078 GGTGCATACCACCATACCCAGTTAATTTTTATATATTTTTTGTAGAGATGGGGTTTCTCCATGTT GGTGCATACCACCATACCCAGTTAATTTTTATGTATTTTTTGTAGAGATGGGGTTTCTCCATGTT T C QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs576239406 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10931 29410 RMVar_ID_29410 Human_SNP_ID_132422065 A-to-I Human chr3 - 49084677 49084677 49084677 TCACTACAACCTCCGCCTCCCGGATTCAAGCAATTCTCCTGCCTCAGCCTCTAGAGTAGCTGGGA TCACTACAACCTCCGCCTCCCGGATTCAAGCAGTTCTCCTGCCTCAGCCTCTAGAGTAGCTGGGA T C QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1034647814 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10931 29411 RMVar_ID_29411 Human_SNP_ID_132422187 A-to-I Human chr3 - 49085021 49085021 49085021 CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCCAACACCACACCCGGCTAATTTTT CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTGCAGGCGCCCAACACCACACCCGGCTAATTTTT T C QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1437036632 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10931 29412 RMVar_ID_29412 Human_SNP_ID_132422772 A-to-I Human chr3 - 49087077 49087077 49087077 AATTTTTGTGTTTTTGGTAGAGATGGGATTTCACCACGTTGGCCAGACTGGTCTTGAACTCCCAA AATTTTTGTGTTTTTGGTAGAGATGGGATTTCGCCACGTTGGCCAGACTGGTCTTGAACTCCCAA T C QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1410858650 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22726129 Human_Splice_Rec_427318 RMVar_hsa_circ_10931 29413 RMVar_ID_29413 Human_SNP_ID_132422895 A-to-I Human chr3 - 49087459 49087459 49087459 CTCACTGCAACCTTCGCCTCCCGGGTTCAAGTAATTCTCCTGCCTCAGCTTCCCTAGTAGCTGGG CTCACTGCAACCTTCGCCTCCCGGGTTCAAGTGATTCTCCTGCCTCAGCTTCCCTAGTAGCTGGG T C QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1232796859 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10931 29414 RMVar_ID_29414 Human_SNP_ID_132422972 A-to-I Human chr3 - 49087711 49087711 49087711 TGGTACCCCGCCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGC TGGTACCCCGCCTGGCTAATTTTTGTATTTTTGGTAGAGATGGGGTTTCACCATGTTGGCCAGGC T C QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1474665604 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10931 29415 RMVar_ID_29415 Human_SNP_ID_132422975 A-to-I Human chr3 - 49087726 49087726 49087726 GGGACTACAGGCGCATGGTACCCCGCCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCA GGGACTACAGGCGCATGGTACCCCGCCTGGCTTATTTTTGTATTTTTAGTAGAGATGGGGTTTCA T A QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1045371942 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10931 29416 RMVar_ID_29416 Human_SNP_ID_132423157 A-to-I Human chr3 - 49088116 49088116 49088116 ACTTTCTCTCTACTAAAAAATACAAAAAAATTAGCTGGATGTGGTGGCGGGCGCCTGTGGTCCCA ACTTTCTCTCTACTAAAAAATACAAAAAAATTGGCTGGATGTGGTGGCGGGCGCCTGTGGTCCCA T C QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1385639690 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10931 29417 RMVar_ID_29417 Human_SNP_ID_132423261 A-to-I Human chr3 - 49088460 49088455 49088460 AACCCCGATTCTACTAAAAATACAAAAAAATTAGCTGGGCTGGGTGGCGTGCGCCTGTAGTTCAA AACCCCGATTCTACTAAAAATACAAAAAAATT_____GGCTGGGTGGCGTGCGCCTGTAGTTCAA CCAGCT C QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1238073388 Functional Loss DEL dbSNP153 33..37 33 - - - Human_RBP_ID_7204493,Human_RBP_ID_17573652 RMVar_hsa_circ_10931 29418 RMVar_ID_29418 Human_SNP_ID_132426460 A-to-I Human chr3 - 49098628 49098628 49098628 GGGCCAGCCTGTGGGCCTGAGGCATACAGGCTACGTCATTGAGCTGCAGCATGTTGTCAAGGTGA GGGCCAGCCTGTGGGCCTGAGGCATACAGGCTGCGTCATTGAGCTGCAGCATGTTGTCAAGGTGA T C QARS1 Ensembl:ENSG00000172053 Protein coding exon GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1396216642 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_604096,Human_RBP_ID_18012814,Human_RBP_ID_22455436,Human_RBP_ID_25763655 Human_Splice_Rec_427324,Human_Splice_Rec_427325,Human_Splice_Rec_427338,Human_Splice_Rec_427339,Human_Splice_Rec_427358,Human_Splice_Rec_427359,Human_Splice_Rec_427404,Human_Splice_Rec_427405,Human_Splice_Rec_427456,Human_Splice_Rec_427457,Human_Splice_Rec_427502,Human_Splice_Rec_427503,Human_Splice_Rec_427520,Human_Splice_Rec_427521,Human_Splice_Rec_427566,Human_Splice_Rec_427567,Human_Splice_Rec_427575,Human_Splice_Rec_427616,Human_Splice_Rec_427617,Human_Splice_Rec_427636,Human_Splice_Rec_427637,Human_Splice_Rec_427651,Human_Splice_Rec_427690,Human_Splice_Rec_427691,Human_Splice_Rec_427704,Human_Splice_Rec_427705,Human_Splice_Rec_427710,Human_Splice_Rec_427711,Human_Splice_Rec_427744,Human_Splice_Rec_427745,Human_Splice_Rec_427756,Human_Splice_Rec_427757 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,RMVar_hsa_circ_377724 29419 RMVar_ID_29419 Human_SNP_ID_132427677 A-to-I Human chr3 - 49101851 49101851 49101851 GACCCTGTCTCTGATGGAGCAGCTCCGGGGGGAGGCCCTTAAGTTCCACAAGCCTGGTTAGTGGG GACCCTGTCTCTGATGGAGCAGCTCCGGGGGGGGGCCCTTAAGTTCCACAAGCCTGGTTAGTGGG T C QARS1 Ensembl:ENSG00000172053 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs866582768 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_604108,Human_RBP_ID_836197,Human_RBP_ID_938605,Human_RBP_ID_1964565,Human_RBP_ID_3964005,Human_RBP_ID_8875515,Human_RBP_ID_19010296,Human_RBP_ID_26346901,Human_RBP_ID_27822249 Human_Splice_Rec_427380,Human_Splice_Rec_427381,Human_Splice_Rec_427432,Human_Splice_Rec_427433,Human_Splice_Rec_427478,Human_Splice_Rec_427479,Human_Splice_Rec_427542,Human_Splice_Rec_427543,Human_Splice_Rec_427592,Human_Splice_Rec_427593,Human_Splice_Rec_427666,Human_Splice_Rec_427667,Human_Splice_Rec_427720,Human_Splice_Rec_427721,Human_Splice_Rec_427796,Human_Splice_Rec_427797,Human_Splice_Rec_427814,Human_Splice_Rec_427815,Human_Splice_Rec_427836,Human_Splice_Rec_427837,Human_Splice_Rec_427858,Human_Splice_Rec_427859,Human_Splice_Rec_427876,Human_Splice_Rec_427877,Human_Splice_Rec_427896,Human_Splice_Rec_427897,Human_Splice_Rec_427914,Human_Splice_Rec_427915,Human_Splice_Rec_427932,Human_Splice_Rec_427933,Human_Splice_Rec_427950,Human_Splice_Rec_427951,Human_Splice_Rec_427964,Human_Splice_Rec_427965,Human_Splice_Rec_427978,Human_Splice_Rec_427979,Human_Splice_Rec_427994,Human_Splice_Rec_427995,Human_Splice_Rec_428020,Human_Splice_Rec_428032 RMVar_hsa_circ_127195,RMVar_hsa_circ_110504,RMVar_hsa_circ_218066,RMVar_hsa_circ_218067,RMVar_hsa_circ_25559,RMVar_hsa_circ_78406,RMVar_hsa_circ_218068 29420 RMVar_ID_29420 Human_SNP_ID_132445088 A-to-I Human chr3 - 49162752 49162752 49162752 TGGGGAAACTAAGCCCAGCTGTCTGTGTGGCTAGTGGCACAGTGTGCTATGTCCGTGGACTCCAC TGGGGAAACTAAGCCCAGCTGTCTGTGTGGCTCGTGGCACAGTGTGCTATGTCCGTGGACTCCAC T G CCDC71 Ensembl:ENSG00000177352 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs553765878 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_604135,Human_RBP_ID_4746278,Human_RBP_ID_22282763 29421 RMVar_ID_29421 Human_SNP_ID_132455067 A-to-I Human chr3 + 49200278 49200277 49200278 CCTGAGGTCAGGAGCTCGAGACCAGCCTGGCCAACATAGCGAAAACCCGTCTCTACTAAAAATAC CCTGAGGTCAGGAGCTCGAGACCAGCCTGGCC_ACATAGCGAAAACCCGTCTCTACTAAAAATAC CA C CCDC36 Ensembl:ENSG00000173421 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1219271585 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_29525 29422 RMVar_ID_29422 Human_SNP_ID_132455071 A-to-I Human chr3 + 49200283 49200283 49200283 GGTCAGGAGCTCGAGACCAGCCTGGCCAACATAGCGAAAACCCGTCTCTACTAAAAATACAAAAA GGTCAGGAGCTCGAGACCAGCCTGGCCAACATGGCGAAAACCCGTCTCTACTAAAAATACAAAAA A G CCDC36 Ensembl:ENSG00000173421 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1213962116 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29525 29423 RMVar_ID_29423 Human_SNP_ID_132472756 A-to-I Human chr3 - 49270661 49270661 49270661 AAAATTAGCCAGGAGTGGTGGTGTGCACCTGTAGTCCCAGCTACTTTGGAGGCTGAGGTAGGAGA AAAATTAGCCAGGAGTGGTGGTGTGCACCTGTGGTCCCAGCTACTTTGGAGGCTGAGGTAGGAGA T C C3orf62 Ensembl:ENSG00000188315 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1265990465 Functional Loss SNV dbSNP153 33..33 33 - - - 29424 RMVar_ID_29424 Human_SNP_ID_132473964 A-to-I Human chr3 + 49275213 49275212 49275213 TCAGCTCACTGCAACCTCTGCCTCCAGGATTCAAGCAATTCTCCTGCCTCGGCCTCCCAAGTAGC TCAGCTCACTGCAACCTCTGCCTCCAGGATTC_AGCAATTCTCCTGCCTCGGCCTCCCAAGTAGC CA C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1165488442 Functional Loss DEL dbSNP153 33..33 33 - - - 29425 RMVar_ID_29425 Human_SNP_ID_132475809 A-to-I Human chr3 - 49281200 49281200 49281200 CGCCTGCCTTGGCCTCCGAAAGTGCTGGGATTACAGGTGTGAGCCACCGTGCGCGGCCTAATTTT CGCCTGCCTTGGCCTCCGAAAGTGCTGGGATTGCAGGTGTGAGCCACCGTGCGCGGCCTAATTTT T C USP4 Ensembl:ENSG00000114316 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1032019604 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122926,RMVar_hsa_circ_41655,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124 29426 RMVar_ID_29426 Human_SNP_ID_132475821 A-to-I Human chr3 - 49281252 49281252 49281252 CAGGGTTTCACCGTGTTAGCCAGGATGGTCTCAATCTTCTGATCTCGTGATCCGCCTGCCTTGGC CAGGGTTTCACCGTGTTAGCCAGGATGGTCTCGATCTTCTGATCTCGTGATCCGCCTGCCTTGGC T C USP4 Ensembl:ENSG00000114316 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1390258835 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122926,RMVar_hsa_circ_41655,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124 29427 RMVar_ID_29427 Human_SNP_ID_132476122 A-to-I Human chr3 - 49281750 49281750 49281750 CCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGTGCCCGGCCTTTTTTTTTTTTT CCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGTGCCCGGCCTTTTTTTTTTTTT T C USP4 Ensembl:ENSG00000114316 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1336593765 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122926,RMVar_hsa_circ_41655,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124 29428 RMVar_ID_29428 Human_SNP_ID_132476425 A-to-I Human chr3 - 49282845 49282845 49282845 AAATTAGCTGGATGTGGTGGTGCACGCCTGTAATCCCAGCTACTAGGGAGGCTGAGGCAGGAGAA AAATTAGCTGGATGTGGTGGTGCACGCCTGTAGTCCCAGCTACTAGGGAGGCTGAGGCAGGAGAA T C USP4 Ensembl:ENSG00000114316 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs900955126 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122926,RMVar_hsa_circ_41655,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124 29429 RMVar_ID_29429 Human_SNP_ID_132477752 A-to-I Human chr3 - 49287508 49287508 49287508 AGATTGCACCAATGTACTCTAGCCTGGGCAACAGAGTGAGACTCCACTTCAAAAAAAAAGGCAAT AGATTGCACCAATGTACTCTAGCCTGGGCAACGGAGTGAGACTCCACTTCAAAAAAAAAGGCAAT T C USP4 Ensembl:ENSG00000114316 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs576533965 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33186,RMVar_hsa_circ_5849,RMVar_hsa_circ_122926,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124,RMVar_hsa_circ_345892,RMVar_hsa_circ_286328,RMVar_hsa_circ_113824,RMVar_hsa_circ_218125,RMVar_hsa_circ_218127,RMVar_hsa_circ_218126,RMVar_hsa_circ_85294,RMVar_hsa_circ_24924,RMVar_hsa_circ_115601,RMVar_hsa_circ_218131,RMVar_hsa_circ_266947,RMVar_hsa_circ_331728,RMVar_hsa_circ_218132,RMVar_hsa_circ_34719,RMVar_hsa_circ_218134 29430 RMVar_ID_29430 Human_SNP_ID_132477772 A-to-I Human chr3 - 49287610 49287610 49287610 AAATTAGCTGGGCGTGGTGGTGCGTGCCTGTAATCACAGCTATTCAGGAGGCTGAGGCAGCAGAA AAATTAGCTGGGCGTGGTGGTGCGTGCCTGTAGTCACAGCTATTCAGGAGGCTGAGGCAGCAGAA T C USP4 Ensembl:ENSG00000114316 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs749448688 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33186,RMVar_hsa_circ_5849,RMVar_hsa_circ_122926,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124,RMVar_hsa_circ_345892,RMVar_hsa_circ_286328,RMVar_hsa_circ_113824,RMVar_hsa_circ_218125,RMVar_hsa_circ_218127,RMVar_hsa_circ_218126,RMVar_hsa_circ_85294,RMVar_hsa_circ_24924,RMVar_hsa_circ_115601,RMVar_hsa_circ_218131,RMVar_hsa_circ_266947,RMVar_hsa_circ_331728,RMVar_hsa_circ_218132,RMVar_hsa_circ_34719,RMVar_hsa_circ_218134 29431 RMVar_ID_29431 Human_SNP_ID_132478288 A-to-I Human chr3 - 49290086 49290086 49290086 TTTGGTATTTTAGGGTTGAATATGGCTGGAATACAGTGGCGCAATCATGGCTCACTGCAGCCTTG TTTGGTATTTTAGGGTTGAATATGGCTGGAATTCAGTGGCGCAATCATGGCTCACTGCAGCCTTG T A USP4 Ensembl:ENSG00000114316 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs894479785 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33186,RMVar_hsa_circ_5849,RMVar_hsa_circ_122926,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124,RMVar_hsa_circ_345892,RMVar_hsa_circ_286328,RMVar_hsa_circ_113824,RMVar_hsa_circ_218125,RMVar_hsa_circ_218127,RMVar_hsa_circ_218126,RMVar_hsa_circ_85294,RMVar_hsa_circ_24924,RMVar_hsa_circ_115601,RMVar_hsa_circ_218131,RMVar_hsa_circ_266947,RMVar_hsa_circ_331728,RMVar_hsa_circ_218132,RMVar_hsa_circ_34719,RMVar_hsa_circ_218134 29432 RMVar_ID_29432 Human_SNP_ID_132478402 A-to-I Human chr3 - 49290671 49290671 49290671 GTCTCTACTAAAAAATACAAAATTAGCCAGGCATGGCAGTGTGTGCCTGTAATCCCAGCTACTTG GTCTCTACTAAAAAATACAAAATTAGCCAGGCGTGGCAGTGTGTGCCTGTAATCCCAGCTACTTG T C USP4 Ensembl:ENSG00000114316 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs531247152 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33186,RMVar_hsa_circ_5849,RMVar_hsa_circ_122926,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124,RMVar_hsa_circ_345892,RMVar_hsa_circ_286328,RMVar_hsa_circ_113824,RMVar_hsa_circ_218125,RMVar_hsa_circ_218127,RMVar_hsa_circ_218126,RMVar_hsa_circ_85294,RMVar_hsa_circ_24924,RMVar_hsa_circ_115601,RMVar_hsa_circ_218131,RMVar_hsa_circ_266947,RMVar_hsa_circ_331728,RMVar_hsa_circ_218132,RMVar_hsa_circ_34719,RMVar_hsa_circ_218134 29433 RMVar_ID_29433 Human_SNP_ID_132478537 A-to-I Human chr3 - 49291165 49291165 49291165 GGTCAGGAGATCGAAACTATCCTGGCTAACACAGTGAAACCCCATCTCTGCTAAAAATACAAAAA GGTCAGGAGATCGAAACTATCCTGGCTAACACGGTGAAACCCCATCTCTGCTAAAAATACAAAAA T C USP4 Ensembl:ENSG00000114316 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs546349757 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33186,RMVar_hsa_circ_5849,RMVar_hsa_circ_122926,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124,RMVar_hsa_circ_345892,RMVar_hsa_circ_286328,RMVar_hsa_circ_113824,RMVar_hsa_circ_218125,RMVar_hsa_circ_218127,RMVar_hsa_circ_218126,RMVar_hsa_circ_85294,RMVar_hsa_circ_24924,RMVar_hsa_circ_115601,RMVar_hsa_circ_218131,RMVar_hsa_circ_266947,RMVar_hsa_circ_331728,RMVar_hsa_circ_218132,RMVar_hsa_circ_34719,RMVar_hsa_circ_218134 29434 RMVar_ID_29434 Human_SNP_ID_132478813 A-to-I Human chr3 - 49292174 49292174 49292174 TTAAGTGATTGTCCCACCTCAGCCTCCAGAGTAGCTGGGACTACAGGTGCATGCCACGACACCCA TTAAGTGATTGTCCCACCTCAGCCTCCAGAGTGGCTGGGACTACAGGTGCATGCCACGACACCCA T C USP4 Ensembl:ENSG00000114316 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs976605556 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33186,RMVar_hsa_circ_5849,RMVar_hsa_circ_122926,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124,RMVar_hsa_circ_345892,RMVar_hsa_circ_286328,RMVar_hsa_circ_113824,RMVar_hsa_circ_218125,RMVar_hsa_circ_218127,RMVar_hsa_circ_218126,RMVar_hsa_circ_85294,RMVar_hsa_circ_24924,RMVar_hsa_circ_115601,RMVar_hsa_circ_218131,RMVar_hsa_circ_266947,RMVar_hsa_circ_331728,RMVar_hsa_circ_218132,RMVar_hsa_circ_34719,RMVar_hsa_circ_218134 29435 RMVar_ID_29435 Human_SNP_ID_132482995 A-to-I Human chr3 - 49308374 49308374 49308374 CGGAGGTTGCAATGAGCCAAGATCATGCCACTACACTCCAGCCTGGGTGACAGTGTGAGACTCTG CGGAGGTTGCAATGAGCCAAGATCATGCCACTGCACTCCAGCCTGGGTGACAGTGTGAGACTCTG T C USP4 Ensembl:ENSG00000114316 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs200383467 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1148,RMVar_hsa_circ_122926,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124,RMVar_hsa_circ_113824,RMVar_hsa_circ_218125,RMVar_hsa_circ_85294,RMVar_hsa_circ_218131,RMVar_hsa_circ_18244,RMVar_hsa_circ_373260,RMVar_hsa_circ_99739,RMVar_hsa_circ_103383,RMVar_hsa_circ_9600,RMVar_hsa_circ_218140,RMVar_hsa_circ_218141,RMVar_hsa_circ_218139,RMVar_hsa_circ_23838,RMVar_hsa_circ_126788,RMVar_hsa_circ_218142,RMVar_hsa_circ_91230,RMVar_hsa_circ_350836,RMVar_hsa_circ_125785,RMVar_hsa_circ_218143,RMVar_hsa_circ_218144,RMVar_hsa_circ_218145,RMVar_hsa_circ_299119,RMVar_hsa_circ_34048,RMVar_hsa_circ_218148,RMVar_hsa_circ_278646,RMVar_hsa_circ_218147,RMVar_hsa_circ_360540,RMVar_hsa_circ_279635,RMVar_hsa_circ_38739,RMVar_hsa_circ_218149,RMVar_hsa_circ_218150 29436 RMVar_ID_29436 Human_SNP_ID_132483116 A-to-I Human chr3 - 49308945 49308945 49308945 GCACTGCAACCTCCACCTCCTGGGTTTAAGCAATTCTCATGCCTCAGCCTCCCGAGTAGCTGGGA GCACTGCAACCTCCACCTCCTGGGTTTAAGCAGTTCTCATGCCTCAGCCTCCCGAGTAGCTGGGA T C USP4 Ensembl:ENSG00000114316 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1436669616 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1148,RMVar_hsa_circ_122926,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124,RMVar_hsa_circ_113824,RMVar_hsa_circ_218125,RMVar_hsa_circ_85294,RMVar_hsa_circ_218131,RMVar_hsa_circ_18244,RMVar_hsa_circ_373260,RMVar_hsa_circ_99739,RMVar_hsa_circ_103383,RMVar_hsa_circ_9600,RMVar_hsa_circ_218140,RMVar_hsa_circ_218141,RMVar_hsa_circ_218139,RMVar_hsa_circ_23838,RMVar_hsa_circ_126788,RMVar_hsa_circ_218142,RMVar_hsa_circ_91230,RMVar_hsa_circ_350836,RMVar_hsa_circ_125785,RMVar_hsa_circ_218143,RMVar_hsa_circ_218144,RMVar_hsa_circ_218145,RMVar_hsa_circ_299119,RMVar_hsa_circ_34048,RMVar_hsa_circ_218148,RMVar_hsa_circ_278646,RMVar_hsa_circ_218147,RMVar_hsa_circ_360540,RMVar_hsa_circ_279635,RMVar_hsa_circ_38739,RMVar_hsa_circ_218149,RMVar_hsa_circ_218150 29437 RMVar_ID_29437 Human_SNP_ID_132483118 A-to-I Human chr3 - 49308949 49308949 49308949 TGACGCACTGCAACCTCCACCTCCTGGGTTTAAGCAATTCTCATGCCTCAGCCTCCCGAGTAGCT TGACGCACTGCAACCTCCACCTCCTGGGTTTAGGCAATTCTCATGCCTCAGCCTCCCGAGTAGCT T C USP4 Ensembl:ENSG00000114316 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1334198336 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1148,RMVar_hsa_circ_122926,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124,RMVar_hsa_circ_113824,RMVar_hsa_circ_218125,RMVar_hsa_circ_85294,RMVar_hsa_circ_218131,RMVar_hsa_circ_18244,RMVar_hsa_circ_373260,RMVar_hsa_circ_99739,RMVar_hsa_circ_103383,RMVar_hsa_circ_9600,RMVar_hsa_circ_218140,RMVar_hsa_circ_218141,RMVar_hsa_circ_218139,RMVar_hsa_circ_23838,RMVar_hsa_circ_126788,RMVar_hsa_circ_218142,RMVar_hsa_circ_91230,RMVar_hsa_circ_350836,RMVar_hsa_circ_125785,RMVar_hsa_circ_218143,RMVar_hsa_circ_218144,RMVar_hsa_circ_218145,RMVar_hsa_circ_299119,RMVar_hsa_circ_34048,RMVar_hsa_circ_218148,RMVar_hsa_circ_278646,RMVar_hsa_circ_218147,RMVar_hsa_circ_360540,RMVar_hsa_circ_279635,RMVar_hsa_circ_38739,RMVar_hsa_circ_218149,RMVar_hsa_circ_218150 29438 RMVar_ID_29438 Human_SNP_ID_132483130 A-to-I Human chr3 - 49308986 49308986 49308986 TCTCTGTTGCCCAGGCTGGAGTGCAGTCGCGCAATCTTGACGCACTGCAACCTCCACCTCCTGGG TCTCTGTTGCCCAGGCTGGAGTGCAGTCGCGCGATCTTGACGCACTGCAACCTCCACCTCCTGGG T C USP4 Ensembl:ENSG00000114316 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs559053459 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1148,RMVar_hsa_circ_122926,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124,RMVar_hsa_circ_113824,RMVar_hsa_circ_218125,RMVar_hsa_circ_85294,RMVar_hsa_circ_218131,RMVar_hsa_circ_18244,RMVar_hsa_circ_373260,RMVar_hsa_circ_99739,RMVar_hsa_circ_103383,RMVar_hsa_circ_9600,RMVar_hsa_circ_218140,RMVar_hsa_circ_218141,RMVar_hsa_circ_218139,RMVar_hsa_circ_23838,RMVar_hsa_circ_126788,RMVar_hsa_circ_218142,RMVar_hsa_circ_91230,RMVar_hsa_circ_350836,RMVar_hsa_circ_125785,RMVar_hsa_circ_218143,RMVar_hsa_circ_218144,RMVar_hsa_circ_218145,RMVar_hsa_circ_299119,RMVar_hsa_circ_34048,RMVar_hsa_circ_218148,RMVar_hsa_circ_278646,RMVar_hsa_circ_218147,RMVar_hsa_circ_360540,RMVar_hsa_circ_279635,RMVar_hsa_circ_38739,RMVar_hsa_circ_218149,RMVar_hsa_circ_218150 29439 RMVar_ID_29439 Human_SNP_ID_132483927 A-to-I Human chr3 - 49311931 49311931 49311931 GCAATCTGCCTGCCTCAGCCTCCCAAAGTACTAGGATTACAGGCACGAGCCACTGCGCCTGGTCA GCAATCTGCCTGCCTCAGCCTCCCAAAGTACTGGGATTACAGGCACGAGCCACTGCGCCTGGTCA T C USP4 Ensembl:ENSG00000114316 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs887379542 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1148,RMVar_hsa_circ_122926,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124,RMVar_hsa_circ_113824,RMVar_hsa_circ_218125,RMVar_hsa_circ_85294,RMVar_hsa_circ_218131,RMVar_hsa_circ_99739,RMVar_hsa_circ_103383,RMVar_hsa_circ_218140,RMVar_hsa_circ_218141,RMVar_hsa_circ_218142,RMVar_hsa_circ_91230,RMVar_hsa_circ_125785,RMVar_hsa_circ_218143,RMVar_hsa_circ_34048,RMVar_hsa_circ_360540,RMVar_hsa_circ_279635,RMVar_hsa_circ_38739,RMVar_hsa_circ_218149,RMVar_hsa_circ_218150,RMVar_hsa_circ_334105 29440 RMVar_ID_29440 Human_SNP_ID_132484288 A-to-I Human chr3 - 49313133 49313133 49313133 TAATCCCAGCACTTTGGGAGGCCAAGGCAGGCAGATCACAAGGTCAAGAGCTTGAGACCATTCTG TAATCCCAGCACTTTGGGAGGCCAAGGCAGGCGGATCACAAGGTCAAGAGCTTGAGACCATTCTG T C USP4 Ensembl:ENSG00000114316 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs55709631 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1148,RMVar_hsa_circ_122926,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124,RMVar_hsa_circ_113824,RMVar_hsa_circ_218125,RMVar_hsa_circ_85294,RMVar_hsa_circ_218131,RMVar_hsa_circ_99739,RMVar_hsa_circ_103383,RMVar_hsa_circ_218140,RMVar_hsa_circ_218141,RMVar_hsa_circ_218142,RMVar_hsa_circ_91230,RMVar_hsa_circ_125785,RMVar_hsa_circ_218143,RMVar_hsa_circ_34048,RMVar_hsa_circ_360540,RMVar_hsa_circ_279635,RMVar_hsa_circ_38739,RMVar_hsa_circ_218149,RMVar_hsa_circ_218150,RMVar_hsa_circ_334105 29441 RMVar_ID_29441 Human_SNP_ID_132484336 A-to-I Human chr3 - 49313364 49313364 49313364 GCCACTAGGCCTGGCTAATTTTTTTTATTTTTAGTAGAGACGGGGTTCCACCACGTTGGTAAGGC GCCACTAGGCCTGGCTAATTTTTTTTATTTTTGGTAGAGACGGGGTTCCACCACGTTGGTAAGGC T C USP4 Ensembl:ENSG00000114316 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1182484869 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1148,RMVar_hsa_circ_122926,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124,RMVar_hsa_circ_113824,RMVar_hsa_circ_218125,RMVar_hsa_circ_85294,RMVar_hsa_circ_218131,RMVar_hsa_circ_99739,RMVar_hsa_circ_103383,RMVar_hsa_circ_218140,RMVar_hsa_circ_218141,RMVar_hsa_circ_218142,RMVar_hsa_circ_91230,RMVar_hsa_circ_125785,RMVar_hsa_circ_218143,RMVar_hsa_circ_34048,RMVar_hsa_circ_360540,RMVar_hsa_circ_279635,RMVar_hsa_circ_38739,RMVar_hsa_circ_218149,RMVar_hsa_circ_218150,RMVar_hsa_circ_334105 29442 RMVar_ID_29442 Human_SNP_ID_132484337 A-to-I Human chr3 - 49313370 49313370 49313370 GCATGCGCCACTAGGCCTGGCTAATTTTTTTTATTTTTAGTAGAGACGGGGTTCCACCACGTTGG GCATGCGCCACTAGGCCTGGCTAATTTTTTTTGTTTTTAGTAGAGACGGGGTTCCACCACGTTGG T C USP4 Ensembl:ENSG00000114316 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1167439228 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1148,RMVar_hsa_circ_122926,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124,RMVar_hsa_circ_113824,RMVar_hsa_circ_218125,RMVar_hsa_circ_85294,RMVar_hsa_circ_218131,RMVar_hsa_circ_99739,RMVar_hsa_circ_103383,RMVar_hsa_circ_218140,RMVar_hsa_circ_218141,RMVar_hsa_circ_218142,RMVar_hsa_circ_91230,RMVar_hsa_circ_125785,RMVar_hsa_circ_218143,RMVar_hsa_circ_34048,RMVar_hsa_circ_360540,RMVar_hsa_circ_279635,RMVar_hsa_circ_38739,RMVar_hsa_circ_218149,RMVar_hsa_circ_218150,RMVar_hsa_circ_334105 29443 RMVar_ID_29443 Human_SNP_ID_132484709 A-to-I Human chr3 - 49315232 49315232 49315232 GGGATCCTCTCGGCTTAGCCTCCCGAGTAGCTAGGACTGCAGGCACGTGCTGCTATGCCTGGCTT GGGATCCTCTCGGCTTAGCCTCCCGAGTAGCTGGGACTGCAGGCACGTGCTGCTATGCCTGGCTT T C USP4 Ensembl:ENSG00000114316 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs927229298 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1148,RMVar_hsa_circ_122926,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124,RMVar_hsa_circ_113824,RMVar_hsa_circ_218125,RMVar_hsa_circ_85294,RMVar_hsa_circ_218131,RMVar_hsa_circ_99739,RMVar_hsa_circ_103383,RMVar_hsa_circ_218140,RMVar_hsa_circ_218141,RMVar_hsa_circ_218142,RMVar_hsa_circ_91230,RMVar_hsa_circ_125785,RMVar_hsa_circ_218143,RMVar_hsa_circ_34048,RMVar_hsa_circ_360540,RMVar_hsa_circ_279635,RMVar_hsa_circ_38739,RMVar_hsa_circ_218149,RMVar_hsa_circ_218150,RMVar_hsa_circ_334105 29444 RMVar_ID_29444 Human_SNP_ID_132484726 A-to-I Human chr3 - 49315309 49315309 49315309 GGGTCTTGCTTTGTTGCCCAGACTGGAATGCAATGGCATGATCATAGTTCACTGCAACCTCAAAC GGGTCTTGCTTTGTTGCCCAGACTGGAATGCAGTGGCATGATCATAGTTCACTGCAACCTCAAAC T C USP4 Ensembl:ENSG00000114316 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1386757924 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1148,RMVar_hsa_circ_122926,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124,RMVar_hsa_circ_113824,RMVar_hsa_circ_218125,RMVar_hsa_circ_85294,RMVar_hsa_circ_218131,RMVar_hsa_circ_99739,RMVar_hsa_circ_103383,RMVar_hsa_circ_218140,RMVar_hsa_circ_218141,RMVar_hsa_circ_218142,RMVar_hsa_circ_91230,RMVar_hsa_circ_125785,RMVar_hsa_circ_218143,RMVar_hsa_circ_34048,RMVar_hsa_circ_360540,RMVar_hsa_circ_279635,RMVar_hsa_circ_38739,RMVar_hsa_circ_218149,RMVar_hsa_circ_218150,RMVar_hsa_circ_334105 29445 RMVar_ID_29445 Human_SNP_ID_132484877 A-to-I Human chr3 - 49316054 49316054 49316054 GAATTACAGGCATGTGCCACCATGCCTGGCTAATTTTGTATTTTTAGTAGAGATGGGGTTCCTCT GAATTACAGGCATGTGCCACCATGCCTGGCTAGTTTTGTATTTTTAGTAGAGATGGGGTTCCTCT T C USP4 Ensembl:ENSG00000114316 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1222729990 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1148,RMVar_hsa_circ_122926,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124,RMVar_hsa_circ_113824,RMVar_hsa_circ_218125,RMVar_hsa_circ_85294,RMVar_hsa_circ_218131,RMVar_hsa_circ_99739,RMVar_hsa_circ_103383,RMVar_hsa_circ_218140,RMVar_hsa_circ_218141,RMVar_hsa_circ_218142,RMVar_hsa_circ_91230,RMVar_hsa_circ_125785,RMVar_hsa_circ_218143,RMVar_hsa_circ_34048,RMVar_hsa_circ_360540,RMVar_hsa_circ_279635,RMVar_hsa_circ_38739,RMVar_hsa_circ_218149,RMVar_hsa_circ_218150,RMVar_hsa_circ_334105 29446 RMVar_ID_29446 Human_SNP_ID_132484904 A-to-I Human chr3 - 49316163 49316163 49316163 AGTCTCGCTCTCATTTCCCAGTCTGGAGTGCAATGGCGCGATCTCGGCTCACTGCAACCTCCACC AGTCTCGCTCTCATTTCCCAGTCTGGAGTGCAGTGGCGCGATCTCGGCTCACTGCAACCTCCACC T C USP4 Ensembl:ENSG00000114316 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs374230766 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1148,RMVar_hsa_circ_122926,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124,RMVar_hsa_circ_113824,RMVar_hsa_circ_218125,RMVar_hsa_circ_85294,RMVar_hsa_circ_218131,RMVar_hsa_circ_99739,RMVar_hsa_circ_103383,RMVar_hsa_circ_218140,RMVar_hsa_circ_218141,RMVar_hsa_circ_218142,RMVar_hsa_circ_91230,RMVar_hsa_circ_125785,RMVar_hsa_circ_218143,RMVar_hsa_circ_34048,RMVar_hsa_circ_360540,RMVar_hsa_circ_279635,RMVar_hsa_circ_38739,RMVar_hsa_circ_218149,RMVar_hsa_circ_218150,RMVar_hsa_circ_334105 29447 RMVar_ID_29447 Human_SNP_ID_132484970 A-to-I Human chr3 - 49316457 49316457 49316457 AAAATAGCCAGGCATAGTGGCATGCACCTGTAATTCCAGCTACTCGGGAGGCTGAGGCATGAGAA AAAATAGCCAGGCATAGTGGCATGCACCTGTACTTCCAGCTACTCGGGAGGCTGAGGCATGAGAA T G USP4 Ensembl:ENSG00000114316 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1328652432 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1148,RMVar_hsa_circ_122926,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124,RMVar_hsa_circ_113824,RMVar_hsa_circ_218125,RMVar_hsa_circ_85294,RMVar_hsa_circ_218131,RMVar_hsa_circ_99739,RMVar_hsa_circ_103383,RMVar_hsa_circ_218140,RMVar_hsa_circ_218141,RMVar_hsa_circ_218142,RMVar_hsa_circ_91230,RMVar_hsa_circ_125785,RMVar_hsa_circ_218143,RMVar_hsa_circ_34048,RMVar_hsa_circ_360540,RMVar_hsa_circ_279635,RMVar_hsa_circ_38739,RMVar_hsa_circ_218149,RMVar_hsa_circ_218150,RMVar_hsa_circ_334105 29448 RMVar_ID_29448 Human_SNP_ID_132484975 A-to-I Human chr3 - 49316484 49316484 49316484 TAAAACCCTGTCTCTACTAAAAATAAAAAAATAGCCAGGCATAGTGGCATGCACCTGTAATTCCA TAAAACCCTGTCTCTACTAAAAATAAAAAAATTGCCAGGCATAGTGGCATGCACCTGTAATTCCA T A USP4 Ensembl:ENSG00000114316 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1174931157 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1148,RMVar_hsa_circ_122926,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124,RMVar_hsa_circ_113824,RMVar_hsa_circ_218125,RMVar_hsa_circ_85294,RMVar_hsa_circ_218131,RMVar_hsa_circ_99739,RMVar_hsa_circ_103383,RMVar_hsa_circ_218140,RMVar_hsa_circ_218141,RMVar_hsa_circ_218142,RMVar_hsa_circ_91230,RMVar_hsa_circ_125785,RMVar_hsa_circ_218143,RMVar_hsa_circ_34048,RMVar_hsa_circ_360540,RMVar_hsa_circ_279635,RMVar_hsa_circ_38739,RMVar_hsa_circ_218149,RMVar_hsa_circ_218150,RMVar_hsa_circ_334105 29449 RMVar_ID_29449 Human_SNP_ID_132485628 A-to-I Human chr3 - 49318746 49318746 49318746 GCCACCACGCCCGGCTAATTTTTTGTATTTTTAGTAGAGATGGGATTTCACCACGTTGGCCAGGC GCCACCACGCCCGGCTAATTTTTTGTATTTTTTGTAGAGATGGGATTTCACCACGTTGGCCAGGC T A USP4 Ensembl:ENSG00000114316 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1280038556 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1148,RMVar_hsa_circ_122926,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124,RMVar_hsa_circ_113824,RMVar_hsa_circ_218125,RMVar_hsa_circ_85294,RMVar_hsa_circ_218131,RMVar_hsa_circ_99739,RMVar_hsa_circ_103383,RMVar_hsa_circ_218140,RMVar_hsa_circ_218141,RMVar_hsa_circ_218142,RMVar_hsa_circ_91230,RMVar_hsa_circ_125785,RMVar_hsa_circ_218143,RMVar_hsa_circ_34048,RMVar_hsa_circ_360540,RMVar_hsa_circ_279635,RMVar_hsa_circ_38739,RMVar_hsa_circ_218149,RMVar_hsa_circ_218150,RMVar_hsa_circ_218153,RMVar_hsa_circ_334105 29450 RMVar_ID_29450 Human_SNP_ID_132485631 A-to-I Human chr3 - 49318762 49318762 49318762 GGGATTACGGGTTCGTGCCACCACGCCCGGCTAATTTTTTGTATTTTTAGTAGAGATGGGATTTC GGGATTACGGGTTCGTGCCACCACGCCCGGCTGATTTTTTGTATTTTTAGTAGAGATGGGATTTC T C USP4 Ensembl:ENSG00000114316 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs985640647 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25770904 RMVar_hsa_circ_1148,RMVar_hsa_circ_122926,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124,RMVar_hsa_circ_113824,RMVar_hsa_circ_218125,RMVar_hsa_circ_85294,RMVar_hsa_circ_218131,RMVar_hsa_circ_99739,RMVar_hsa_circ_103383,RMVar_hsa_circ_218140,RMVar_hsa_circ_218141,RMVar_hsa_circ_218142,RMVar_hsa_circ_91230,RMVar_hsa_circ_125785,RMVar_hsa_circ_218143,RMVar_hsa_circ_34048,RMVar_hsa_circ_360540,RMVar_hsa_circ_279635,RMVar_hsa_circ_38739,RMVar_hsa_circ_218149,RMVar_hsa_circ_218150,RMVar_hsa_circ_218153,RMVar_hsa_circ_334105 29451 RMVar_ID_29451 Human_SNP_ID_132485647 A-to-I Human chr3 - 49318788 49318788 49318788 CTCCTGCCTCAGCCTCCTGAGCAGCTGGGATTACGGGTTCGTGCCACCACGCCCGGCTAATTTTT CTCCTGCCTCAGCCTCCTGAGCAGCTGGGATTTCGGGTTCGTGCCACCACGCCCGGCTAATTTTT T A USP4 Ensembl:ENSG00000114316 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs902442733 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1148,RMVar_hsa_circ_122926,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124,RMVar_hsa_circ_113824,RMVar_hsa_circ_218125,RMVar_hsa_circ_85294,RMVar_hsa_circ_218131,RMVar_hsa_circ_99739,RMVar_hsa_circ_103383,RMVar_hsa_circ_218140,RMVar_hsa_circ_218141,RMVar_hsa_circ_218142,RMVar_hsa_circ_91230,RMVar_hsa_circ_125785,RMVar_hsa_circ_218143,RMVar_hsa_circ_34048,RMVar_hsa_circ_360540,RMVar_hsa_circ_279635,RMVar_hsa_circ_38739,RMVar_hsa_circ_218149,RMVar_hsa_circ_218150,RMVar_hsa_circ_218153,RMVar_hsa_circ_334105 29452 RMVar_ID_29452 Human_SNP_ID_132485659 A-to-I Human chr3 - 49318834 49318834 49318834 ACGATCTCGGCTCACTGCAACCTCTGCCTCTCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTG ACGATCTCGGCTCACTGCAACCTCTGCCTCTCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTG T C USP4 Ensembl:ENSG00000114316 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1285969518 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1148,RMVar_hsa_circ_122926,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124,RMVar_hsa_circ_113824,RMVar_hsa_circ_218125,RMVar_hsa_circ_85294,RMVar_hsa_circ_218131,RMVar_hsa_circ_99739,RMVar_hsa_circ_103383,RMVar_hsa_circ_218140,RMVar_hsa_circ_218141,RMVar_hsa_circ_218142,RMVar_hsa_circ_91230,RMVar_hsa_circ_125785,RMVar_hsa_circ_218143,RMVar_hsa_circ_34048,RMVar_hsa_circ_360540,RMVar_hsa_circ_279635,RMVar_hsa_circ_38739,RMVar_hsa_circ_218149,RMVar_hsa_circ_218150,RMVar_hsa_circ_218153,RMVar_hsa_circ_334105 29453 RMVar_ID_29453 Human_SNP_ID_132485660 A-to-I Human chr3 - 49318848 49318848 49318848 TGGAGTGCAGTGGCACGATCTCGGCTCACTGCAACCTCTGCCTCTCAGGTTCAAGCGATTCTCCT TGGAGTGCAGTGGCACGATCTCGGCTCACTGCCACCTCTGCCTCTCAGGTTCAAGCGATTCTCCT T G USP4 Ensembl:ENSG00000114316 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1448851812 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1148,RMVar_hsa_circ_122926,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124,RMVar_hsa_circ_113824,RMVar_hsa_circ_218125,RMVar_hsa_circ_85294,RMVar_hsa_circ_218131,RMVar_hsa_circ_99739,RMVar_hsa_circ_103383,RMVar_hsa_circ_218140,RMVar_hsa_circ_218141,RMVar_hsa_circ_218142,RMVar_hsa_circ_91230,RMVar_hsa_circ_125785,RMVar_hsa_circ_218143,RMVar_hsa_circ_34048,RMVar_hsa_circ_360540,RMVar_hsa_circ_279635,RMVar_hsa_circ_38739,RMVar_hsa_circ_218149,RMVar_hsa_circ_218150,RMVar_hsa_circ_218153,RMVar_hsa_circ_334105 29454 RMVar_ID_29454 Human_SNP_ID_132485674 A-to-I Human chr3 - 49318908 49318908 49318908 GGTGATGGTGGTTTGTTTTTTTTTTTTTTTTGAGGCAGAGTCTTGCTCTGTCACCCAGGCTGGAG GGTGATGGTGGTTTGTTTTTTTTTTTTTTTTGTGGCAGAGTCTTGCTCTGTCACCCAGGCTGGAG T A USP4 Ensembl:ENSG00000114316 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1261989477 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1148,RMVar_hsa_circ_122926,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124,RMVar_hsa_circ_113824,RMVar_hsa_circ_218125,RMVar_hsa_circ_85294,RMVar_hsa_circ_218131,RMVar_hsa_circ_99739,RMVar_hsa_circ_103383,RMVar_hsa_circ_218140,RMVar_hsa_circ_218141,RMVar_hsa_circ_218142,RMVar_hsa_circ_91230,RMVar_hsa_circ_125785,RMVar_hsa_circ_218143,RMVar_hsa_circ_34048,RMVar_hsa_circ_360540,RMVar_hsa_circ_279635,RMVar_hsa_circ_38739,RMVar_hsa_circ_218149,RMVar_hsa_circ_218150,RMVar_hsa_circ_218153,RMVar_hsa_circ_334105 29455 RMVar_ID_29455 Human_SNP_ID_132485732 A-to-I Human chr3 - 49319120 49319120 49319120 TTTTTTTTTTTGAGATGCAGTCTTGCTCTGTCACCCAAGCAGGAGTGCAGTGGCGCAATCCCTCC TTTTTTTTTTTGAGATGCAGTCTTGCTCTGTCGCCCAAGCAGGAGTGCAGTGGCGCAATCCCTCC T C USP4 Ensembl:ENSG00000114316 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs991348334 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22480627 RMVar_hsa_circ_1148,RMVar_hsa_circ_122926,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124,RMVar_hsa_circ_113824,RMVar_hsa_circ_218125,RMVar_hsa_circ_85294,RMVar_hsa_circ_218131,RMVar_hsa_circ_99739,RMVar_hsa_circ_103383,RMVar_hsa_circ_218140,RMVar_hsa_circ_218141,RMVar_hsa_circ_218142,RMVar_hsa_circ_91230,RMVar_hsa_circ_125785,RMVar_hsa_circ_218143,RMVar_hsa_circ_34048,RMVar_hsa_circ_360540,RMVar_hsa_circ_279635,RMVar_hsa_circ_38739,RMVar_hsa_circ_218149,RMVar_hsa_circ_218150,RMVar_hsa_circ_218153,RMVar_hsa_circ_334105 29456 RMVar_ID_29456 Human_SNP_ID_132485806 A-to-I Human chr3 - 49319387 49319387 49319387 AAAATTAGCTGGGTGTGATGGCATGCTCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTAGCTGGGTGTGATGGCATGCTCCTGTTGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA T A USP4 Ensembl:ENSG00000114316 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1382637218 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_154390 RMVar_hsa_circ_1148,RMVar_hsa_circ_122926,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124,RMVar_hsa_circ_113824,RMVar_hsa_circ_218125,RMVar_hsa_circ_85294,RMVar_hsa_circ_218131,RMVar_hsa_circ_99739,RMVar_hsa_circ_103383,RMVar_hsa_circ_218140,RMVar_hsa_circ_218141,RMVar_hsa_circ_218142,RMVar_hsa_circ_91230,RMVar_hsa_circ_125785,RMVar_hsa_circ_218143,RMVar_hsa_circ_34048,RMVar_hsa_circ_360540,RMVar_hsa_circ_279635,RMVar_hsa_circ_38739,RMVar_hsa_circ_218149,RMVar_hsa_circ_218150,RMVar_hsa_circ_218153,RMVar_hsa_circ_334105 29457 RMVar_ID_29457 Human_SNP_ID_132485827 A-to-I Human chr3 - 49319471 49319471 49319471 CAGAGGCAGGCACATCACGAGGTCAAGAGATCAAGACCATCCTGGGCCAATATGGTGAAACCCCG CAGAGGCAGGCACATCACGAGGTCAAGAGATCCAGACCATCCTGGGCCAATATGGTGAAACCCCG T G USP4 Ensembl:ENSG00000114316 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1315676549 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10098405 RMVar_hsa_circ_1148,RMVar_hsa_circ_122926,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124,RMVar_hsa_circ_113824,RMVar_hsa_circ_218125,RMVar_hsa_circ_85294,RMVar_hsa_circ_218131,RMVar_hsa_circ_99739,RMVar_hsa_circ_103383,RMVar_hsa_circ_218140,RMVar_hsa_circ_218141,RMVar_hsa_circ_218142,RMVar_hsa_circ_91230,RMVar_hsa_circ_125785,RMVar_hsa_circ_218143,RMVar_hsa_circ_34048,RMVar_hsa_circ_360540,RMVar_hsa_circ_279635,RMVar_hsa_circ_38739,RMVar_hsa_circ_218149,RMVar_hsa_circ_218150,RMVar_hsa_circ_218153,RMVar_hsa_circ_334105 29458 RMVar_ID_29458 Human_SNP_ID_132485836 A-to-I Human chr3 - 49319523 49319523 49319523 TTGAGGGAATGGAAATAGTGGCTTATGCCTGTAATCCCAGCACTTTGGGAGGCAGAGGCAGGCAC TTGAGGGAATGGAAATAGTGGCTTATGCCTGTTATCCCAGCACTTTGGGAGGCAGAGGCAGGCAC T A USP4 Ensembl:ENSG00000114316 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1559476922 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1148,RMVar_hsa_circ_122926,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124,RMVar_hsa_circ_113824,RMVar_hsa_circ_218125,RMVar_hsa_circ_85294,RMVar_hsa_circ_218131,RMVar_hsa_circ_99739,RMVar_hsa_circ_103383,RMVar_hsa_circ_218140,RMVar_hsa_circ_218141,RMVar_hsa_circ_218142,RMVar_hsa_circ_91230,RMVar_hsa_circ_125785,RMVar_hsa_circ_218143,RMVar_hsa_circ_34048,RMVar_hsa_circ_360540,RMVar_hsa_circ_279635,RMVar_hsa_circ_38739,RMVar_hsa_circ_218149,RMVar_hsa_circ_218150,RMVar_hsa_circ_218153,RMVar_hsa_circ_334105 29459 RMVar_ID_29459 Human_SNP_ID_132485891 A-to-I Human chr3 - 49319778 49319778 49319778 GACCCCCCTATCTACTAAAAGTACAGAAAATTAGCCAGGAGTGGTGGCGTGCACCTGTAATCCCA GACCCCCCTATCTACTAAAAGTACAGAAAATTGGCCAGGAGTGGTGGCGTGCACCTGTAATCCCA T C USP4 Ensembl:ENSG00000114316 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs376720715 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1148,RMVar_hsa_circ_122926,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124,RMVar_hsa_circ_113824,RMVar_hsa_circ_218125,RMVar_hsa_circ_85294,RMVar_hsa_circ_218131,RMVar_hsa_circ_99739,RMVar_hsa_circ_103383,RMVar_hsa_circ_218140,RMVar_hsa_circ_218141,RMVar_hsa_circ_218142,RMVar_hsa_circ_91230,RMVar_hsa_circ_125785,RMVar_hsa_circ_218143,RMVar_hsa_circ_34048,RMVar_hsa_circ_360540,RMVar_hsa_circ_279635,RMVar_hsa_circ_38739,RMVar_hsa_circ_218149,RMVar_hsa_circ_218150,RMVar_hsa_circ_218153,RMVar_hsa_circ_334105 29460 RMVar_ID_29460 Human_SNP_ID_132485892 A-to-I Human chr3 - 49319778 49319778 49319778 GACCCCCCTATCTACTAAAAGTACAGAAAATTAGCCAGGAGTGGTGGCGTGCACCTGTAATCCCA GACCCCCCTATCTACTAAAAGTACAGAAAATTCGCCAGGAGTGGTGGCGTGCACCTGTAATCCCA T G USP4 Ensembl:ENSG00000114316 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs376720715 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1148,RMVar_hsa_circ_122926,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124,RMVar_hsa_circ_113824,RMVar_hsa_circ_218125,RMVar_hsa_circ_85294,RMVar_hsa_circ_218131,RMVar_hsa_circ_99739,RMVar_hsa_circ_103383,RMVar_hsa_circ_218140,RMVar_hsa_circ_218141,RMVar_hsa_circ_218142,RMVar_hsa_circ_91230,RMVar_hsa_circ_125785,RMVar_hsa_circ_218143,RMVar_hsa_circ_34048,RMVar_hsa_circ_360540,RMVar_hsa_circ_279635,RMVar_hsa_circ_38739,RMVar_hsa_circ_218149,RMVar_hsa_circ_218150,RMVar_hsa_circ_218153,RMVar_hsa_circ_334105 29461 RMVar_ID_29461 Human_SNP_ID_132485980 A-to-I Human chr3 - 49320212 49320212 49320212 AGACCCTGTCTCTTGGAAAAAAAGAGTCAGGCATGGTGGCTTATACCTGTAATCCCAACATTTTG AGACCCTGTCTCTTGGAAAAAAAGAGTCAGGCGTGGTGGCTTATACCTGTAATCCCAACATTTTG T C USP4 Ensembl:ENSG00000114316 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs546569213 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1148,RMVar_hsa_circ_122926,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124,RMVar_hsa_circ_113824,RMVar_hsa_circ_218125,RMVar_hsa_circ_85294,RMVar_hsa_circ_218131,RMVar_hsa_circ_99739,RMVar_hsa_circ_103383,RMVar_hsa_circ_218140,RMVar_hsa_circ_218141,RMVar_hsa_circ_218142,RMVar_hsa_circ_91230,RMVar_hsa_circ_125785,RMVar_hsa_circ_218143,RMVar_hsa_circ_34048,RMVar_hsa_circ_360540,RMVar_hsa_circ_279635,RMVar_hsa_circ_38739,RMVar_hsa_circ_218149,RMVar_hsa_circ_218150,RMVar_hsa_circ_218153,RMVar_hsa_circ_334105 29462 RMVar_ID_29462 Human_SNP_ID_132485994 A-to-I Human chr3 - 49320271 49320271 49320271 CGCCCGGCTAATTTTGTATTTTTAGTAGAGACAGGGTTTCTCCATGTTGGTCAGGCTGGAGACCC CGCCCGGCTAATTTTGTATTTTTAGTAGAGACGGGGTTTCTCCATGTTGGTCAGGCTGGAGACCC T C USP4 Ensembl:ENSG00000114316 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs377111745 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2789114 RMVar_hsa_circ_1148,RMVar_hsa_circ_122926,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124,RMVar_hsa_circ_113824,RMVar_hsa_circ_218125,RMVar_hsa_circ_85294,RMVar_hsa_circ_218131,RMVar_hsa_circ_99739,RMVar_hsa_circ_103383,RMVar_hsa_circ_218140,RMVar_hsa_circ_218141,RMVar_hsa_circ_218142,RMVar_hsa_circ_91230,RMVar_hsa_circ_125785,RMVar_hsa_circ_218143,RMVar_hsa_circ_34048,RMVar_hsa_circ_360540,RMVar_hsa_circ_279635,RMVar_hsa_circ_38739,RMVar_hsa_circ_218149,RMVar_hsa_circ_218150,RMVar_hsa_circ_218153,RMVar_hsa_circ_334105 29463 RMVar_ID_29463 Human_SNP_ID_132486073 A-to-I Human chr3 - 49320539 49320539 49320539 AGAAGGCTGAGGGAGGAAGCTTGCTTGAGCCCAGGAGTTCGAAGTTACCGTGAGCCACGATTGCA AGAAGGCTGAGGGAGGAAGCTTGCTTGAGCCCGGGAGTTCGAAGTTACCGTGAGCCACGATTGCA T C USP4 Ensembl:ENSG00000114316 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs769842496 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1148,RMVar_hsa_circ_122926,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124,RMVar_hsa_circ_113824,RMVar_hsa_circ_218125,RMVar_hsa_circ_85294,RMVar_hsa_circ_218131,RMVar_hsa_circ_99739,RMVar_hsa_circ_103383,RMVar_hsa_circ_218140,RMVar_hsa_circ_218141,RMVar_hsa_circ_218142,RMVar_hsa_circ_91230,RMVar_hsa_circ_125785,RMVar_hsa_circ_218143,RMVar_hsa_circ_34048,RMVar_hsa_circ_360540,RMVar_hsa_circ_279635,RMVar_hsa_circ_38739,RMVar_hsa_circ_218149,RMVar_hsa_circ_218150,RMVar_hsa_circ_218153,RMVar_hsa_circ_334105 29464 RMVar_ID_29464 Human_SNP_ID_132486294 A-to-I Human chr3 - 49321606 49321590 49321607 AAAATTAGCCCGGTGCAGTGGCACATGCCTGTAATCGTAGCTACTGGGGAGGCTGAGGCATGAGA AAAATTAGCCCGGTGCAGTGGCACATGCCTG_________________GAGGCTGAGGCATGAGA CCCCAGTAGCTACGATTA C USP4 Ensembl:ENSG00000114316 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1427245063 Functional Loss DEL dbSNP153 32..48 33 - - - Human_RBP_ID_14866041 RMVar_hsa_circ_1148,RMVar_hsa_circ_122926,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124,RMVar_hsa_circ_113824,RMVar_hsa_circ_218125,RMVar_hsa_circ_85294,RMVar_hsa_circ_218131,RMVar_hsa_circ_99739,RMVar_hsa_circ_103383,RMVar_hsa_circ_218140,RMVar_hsa_circ_218141,RMVar_hsa_circ_218142,RMVar_hsa_circ_91230,RMVar_hsa_circ_125785,RMVar_hsa_circ_218143,RMVar_hsa_circ_34048,RMVar_hsa_circ_360540,RMVar_hsa_circ_279635,RMVar_hsa_circ_38739,RMVar_hsa_circ_218149,RMVar_hsa_circ_218150,RMVar_hsa_circ_218153,RMVar_hsa_circ_334105 29465 RMVar_ID_29465 Human_SNP_ID_132486296 A-to-I Human chr3 - 49321596 49321596 49321596 CGGTGCAGTGGCACATGCCTGTAATCGTAGCTACTGGGGAGGCTGAGGCATGAGAATGGTGGTGG CGGTGCAGTGGCACATGCCTGTAATCGTAGCTGCTGGGGAGGCTGAGGCATGAGAATGGTGGTGG T C USP4 Ensembl:ENSG00000114316 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1026393335 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24007883 RMVar_hsa_circ_1148,RMVar_hsa_circ_122926,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124,RMVar_hsa_circ_113824,RMVar_hsa_circ_218125,RMVar_hsa_circ_85294,RMVar_hsa_circ_218131,RMVar_hsa_circ_99739,RMVar_hsa_circ_103383,RMVar_hsa_circ_218140,RMVar_hsa_circ_218141,RMVar_hsa_circ_218142,RMVar_hsa_circ_91230,RMVar_hsa_circ_125785,RMVar_hsa_circ_218143,RMVar_hsa_circ_34048,RMVar_hsa_circ_360540,RMVar_hsa_circ_279635,RMVar_hsa_circ_38739,RMVar_hsa_circ_218149,RMVar_hsa_circ_218150,RMVar_hsa_circ_218153,RMVar_hsa_circ_334105 29466 RMVar_ID_29466 Human_SNP_ID_132486297 A-to-I Human chr3 - 49321596 49321596 49321596 CGGTGCAGTGGCACATGCCTGTAATCGTAGCTACTGGGGAGGCTGAGGCATGAGAATGGTGGTGG CGGTGCAGTGGCACATGCCTGTAATCGTAGCTCCTGGGGAGGCTGAGGCATGAGAATGGTGGTGG T G USP4 Ensembl:ENSG00000114316 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1026393335 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24007883 RMVar_hsa_circ_1148,RMVar_hsa_circ_122926,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124,RMVar_hsa_circ_113824,RMVar_hsa_circ_218125,RMVar_hsa_circ_85294,RMVar_hsa_circ_218131,RMVar_hsa_circ_99739,RMVar_hsa_circ_103383,RMVar_hsa_circ_218140,RMVar_hsa_circ_218141,RMVar_hsa_circ_218142,RMVar_hsa_circ_91230,RMVar_hsa_circ_125785,RMVar_hsa_circ_218143,RMVar_hsa_circ_34048,RMVar_hsa_circ_360540,RMVar_hsa_circ_279635,RMVar_hsa_circ_38739,RMVar_hsa_circ_218149,RMVar_hsa_circ_218150,RMVar_hsa_circ_218153,RMVar_hsa_circ_334105 29467 RMVar_ID_29467 Human_SNP_ID_132486317 A-to-I Human chr3 - 49321690 49321690 49321690 GGCGCCCGGCCAAAAAAAATCAATAATAGGCCAGGTGCGGTGGCTGGCCAACATGCTGAAACCCC GGCGCCCGGCCAAAAAAAATCAATAATAGGCCGGGTGCGGTGGCTGGCCAACATGCTGAAACCCC T C USP4 Ensembl:ENSG00000114316 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1169726028 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1148,RMVar_hsa_circ_122926,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124,RMVar_hsa_circ_113824,RMVar_hsa_circ_218125,RMVar_hsa_circ_85294,RMVar_hsa_circ_218131,RMVar_hsa_circ_99739,RMVar_hsa_circ_103383,RMVar_hsa_circ_218140,RMVar_hsa_circ_218141,RMVar_hsa_circ_218142,RMVar_hsa_circ_91230,RMVar_hsa_circ_125785,RMVar_hsa_circ_218143,RMVar_hsa_circ_34048,RMVar_hsa_circ_360540,RMVar_hsa_circ_279635,RMVar_hsa_circ_38739,RMVar_hsa_circ_218149,RMVar_hsa_circ_218150,RMVar_hsa_circ_218153,RMVar_hsa_circ_334105 29468 RMVar_ID_29468 Human_SNP_ID_132486548 A-to-I Human chr3 - 49322739 49322739 49322739 CTGATGCCTCAGCCTCCCGAGCAGCTGGGACTACAAGCTCCCACCACCATGCCCAGCTAATTTTT CTGATGCCTCAGCCTCCCGAGCAGCTGGGACTGCAAGCTCCCACCACCATGCCCAGCTAATTTTT T C USP4 Ensembl:ENSG00000114316 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1389390378 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1148,RMVar_hsa_circ_122926,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124,RMVar_hsa_circ_113824,RMVar_hsa_circ_218125,RMVar_hsa_circ_85294,RMVar_hsa_circ_218131,RMVar_hsa_circ_99739,RMVar_hsa_circ_103383,RMVar_hsa_circ_218140,RMVar_hsa_circ_218141,RMVar_hsa_circ_218142,RMVar_hsa_circ_91230,RMVar_hsa_circ_125785,RMVar_hsa_circ_218143,RMVar_hsa_circ_34048,RMVar_hsa_circ_360540,RMVar_hsa_circ_279635,RMVar_hsa_circ_38739,RMVar_hsa_circ_218149,RMVar_hsa_circ_218150,RMVar_hsa_circ_218153,RMVar_hsa_circ_334105 29469 RMVar_ID_29469 Human_SNP_ID_132486549 A-to-I Human chr3 - 49322749 49322745 49322750 GTTCAAGTGACTGATGCCTCAGCCTCCCGAGCAGCTGGGACTACAAGCTCCCACCACCATGCCCA GTTCAAGTGACTGATGCCTCAGCCTCCCGAG_____GGGACTACAAGCTCCCACCACCATGCCCA CAGCTG C USP4 Ensembl:ENSG00000114316 Protein coding intron GSE38233;GSE107867;GSE107867 cultured B-cells;ASD brains,frontal_cortex;ASD brains,temporal_cortex - 24183664,30559470,30559470 RNA-Seq:(High) rs1207817519 Functional Loss DEL dbSNP153 32..36 33 - - - Human_RBP_ID_14866065 RMVar_hsa_circ_1148,RMVar_hsa_circ_122926,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124,RMVar_hsa_circ_113824,RMVar_hsa_circ_218125,RMVar_hsa_circ_85294,RMVar_hsa_circ_218131,RMVar_hsa_circ_99739,RMVar_hsa_circ_103383,RMVar_hsa_circ_218140,RMVar_hsa_circ_218141,RMVar_hsa_circ_218142,RMVar_hsa_circ_91230,RMVar_hsa_circ_125785,RMVar_hsa_circ_218143,RMVar_hsa_circ_34048,RMVar_hsa_circ_360540,RMVar_hsa_circ_279635,RMVar_hsa_circ_38739,RMVar_hsa_circ_218149,RMVar_hsa_circ_218150,RMVar_hsa_circ_218153,RMVar_hsa_circ_334105 29470 RMVar_ID_29470 Human_SNP_ID_132486666 A-to-I Human chr3 - 49323170 49323170 49323170 CTGAGGTTGAGAGTTTGAGACCAGCCTGACCAACATGGAGAAACCCTGTCTCTACTAAAAATGCA CTGAGGTTGAGAGTTTGAGACCAGCCTGACCACCATGGAGAAACCCTGTCTCTACTAAAAATGCA T G USP4 Ensembl:ENSG00000114316 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1366883733 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1148,RMVar_hsa_circ_122926,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124,RMVar_hsa_circ_113824,RMVar_hsa_circ_218125,RMVar_hsa_circ_85294,RMVar_hsa_circ_218131,RMVar_hsa_circ_99739,RMVar_hsa_circ_103383,RMVar_hsa_circ_218140,RMVar_hsa_circ_218141,RMVar_hsa_circ_218142,RMVar_hsa_circ_91230,RMVar_hsa_circ_125785,RMVar_hsa_circ_218143,RMVar_hsa_circ_34048,RMVar_hsa_circ_360540,RMVar_hsa_circ_279635,RMVar_hsa_circ_38739,RMVar_hsa_circ_218149,RMVar_hsa_circ_218150,RMVar_hsa_circ_218153,RMVar_hsa_circ_334105 29471 RMVar_ID_29471 Human_SNP_ID_132486840 A-to-I Human chr3 - 49324041 49324041 49324041 TGAGCTGAGATCGCACCATTATACTCCAGCCTAGGTGACAGTGCAAGACTCTGACCCAAAAAAAA TGAGCTGAGATCGCACCATTATACTCCAGCCTGGGTGACAGTGCAAGACTCTGACCCAAAAAAAA T C USP4 Ensembl:ENSG00000114316 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1412588185 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14866113,Human_RBP_ID_25742196 RMVar_hsa_circ_1148,RMVar_hsa_circ_122926,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124,RMVar_hsa_circ_113824,RMVar_hsa_circ_218125,RMVar_hsa_circ_85294,RMVar_hsa_circ_218131,RMVar_hsa_circ_99739,RMVar_hsa_circ_103383,RMVar_hsa_circ_218140,RMVar_hsa_circ_218141,RMVar_hsa_circ_218142,RMVar_hsa_circ_91230,RMVar_hsa_circ_125785,RMVar_hsa_circ_218143,RMVar_hsa_circ_34048,RMVar_hsa_circ_360540,RMVar_hsa_circ_279635,RMVar_hsa_circ_38739,RMVar_hsa_circ_218149,RMVar_hsa_circ_218150,RMVar_hsa_circ_218153,RMVar_hsa_circ_334105 29472 RMVar_ID_29472 Human_SNP_ID_132486859 A-to-I Human chr3 - 49324127 49324127 49324127 AGGCATGGTGGCAGGTACCTGTAATCTCAGCTACTCGGGAGGCTGAGGCTCAAGAGTCGCTTGAA AGGCATGGTGGCAGGTACCTGTAATCTCAGCTTCTCGGGAGGCTGAGGCTCAAGAGTCGCTTGAA T A USP4 Ensembl:ENSG00000114316 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1323450247 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1148,RMVar_hsa_circ_122926,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124,RMVar_hsa_circ_113824,RMVar_hsa_circ_218125,RMVar_hsa_circ_85294,RMVar_hsa_circ_218131,RMVar_hsa_circ_99739,RMVar_hsa_circ_103383,RMVar_hsa_circ_218140,RMVar_hsa_circ_218141,RMVar_hsa_circ_218142,RMVar_hsa_circ_91230,RMVar_hsa_circ_125785,RMVar_hsa_circ_218143,RMVar_hsa_circ_34048,RMVar_hsa_circ_360540,RMVar_hsa_circ_279635,RMVar_hsa_circ_38739,RMVar_hsa_circ_218149,RMVar_hsa_circ_218150,RMVar_hsa_circ_218153,RMVar_hsa_circ_334105 29473 RMVar_ID_29473 Human_SNP_ID_132486860 A-to-I Human chr3 - 49324137 49324137 49324137 AAAATTAGCTAGGCATGGTGGCAGGTACCTGTAATCTCAGCTACTCGGGAGGCTGAGGCTCAAGA AAAATTAGCTAGGCATGGTGGCAGGTACCTGTGATCTCAGCTACTCGGGAGGCTGAGGCTCAAGA T C USP4 Ensembl:ENSG00000114316 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1038101004 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1148,RMVar_hsa_circ_122926,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124,RMVar_hsa_circ_113824,RMVar_hsa_circ_218125,RMVar_hsa_circ_85294,RMVar_hsa_circ_218131,RMVar_hsa_circ_99739,RMVar_hsa_circ_103383,RMVar_hsa_circ_218140,RMVar_hsa_circ_218141,RMVar_hsa_circ_218142,RMVar_hsa_circ_91230,RMVar_hsa_circ_125785,RMVar_hsa_circ_218143,RMVar_hsa_circ_34048,RMVar_hsa_circ_360540,RMVar_hsa_circ_279635,RMVar_hsa_circ_38739,RMVar_hsa_circ_218149,RMVar_hsa_circ_218150,RMVar_hsa_circ_218153,RMVar_hsa_circ_334105 29474 RMVar_ID_29474 Human_SNP_ID_132486870 A-to-I Human chr3 - 49324200 49324200 49324200 GAGGCCAGGAGTTCGAGCCCAGCCTGGTCAACATGGTAAAACCCTGTCTCTACTAAAAATACAAA GAGGCCAGGAGTTCGAGCCCAGCCTGGTCAACGTGGTAAAACCCTGTCTCTACTAAAAATACAAA T C USP4 Ensembl:ENSG00000114316 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs960128176 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1148,RMVar_hsa_circ_122926,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124,RMVar_hsa_circ_113824,RMVar_hsa_circ_218125,RMVar_hsa_circ_85294,RMVar_hsa_circ_218131,RMVar_hsa_circ_99739,RMVar_hsa_circ_103383,RMVar_hsa_circ_218140,RMVar_hsa_circ_218141,RMVar_hsa_circ_218142,RMVar_hsa_circ_91230,RMVar_hsa_circ_125785,RMVar_hsa_circ_218143,RMVar_hsa_circ_34048,RMVar_hsa_circ_360540,RMVar_hsa_circ_279635,RMVar_hsa_circ_38739,RMVar_hsa_circ_218149,RMVar_hsa_circ_218150,RMVar_hsa_circ_218153,RMVar_hsa_circ_334105 29475 RMVar_ID_29475 Human_SNP_ID_132487396 A-to-I Human chr3 - 49326217 49326217 49326217 CACCTCCTGGGTTCAAGCGATTCCCCTGTCTCAGCCTCCTGAGTAGTTGGGATTACAGGCACATG CACCTCCTGGGTTCAAGCGATTCCCCTGTCTCGGCCTCCTGAGTAGTTGGGATTACAGGCACATG T C USP4 Ensembl:ENSG00000114316 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1384099936 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1148,RMVar_hsa_circ_122926,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124,RMVar_hsa_circ_99739,RMVar_hsa_circ_218141,RMVar_hsa_circ_360540,RMVar_hsa_circ_38739,RMVar_hsa_circ_218150,RMVar_hsa_circ_291052,RMVar_hsa_circ_310236,RMVar_hsa_circ_218158,RMVar_hsa_circ_218157,RMVar_hsa_circ_372667 29476 RMVar_ID_29476 Human_SNP_ID_132487490 A-to-I Human chr3 - 49326579 49326579 49326579 CATCCTGGCCAACATGGTGAAATCCTGTCTCTACTAAAAATACAAAAATTAGCTGGGCATGATGG CATCCTGGCCAACATGGTGAAATCCTGTCTCTGCTAAAAATACAAAAATTAGCTGGGCATGATGG T C USP4 Ensembl:ENSG00000114316 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1486165222 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1148,RMVar_hsa_circ_122926,RMVar_hsa_circ_98939,RMVar_hsa_circ_218123,RMVar_hsa_circ_218124,RMVar_hsa_circ_99739,RMVar_hsa_circ_218141,RMVar_hsa_circ_360540,RMVar_hsa_circ_38739,RMVar_hsa_circ_218150,RMVar_hsa_circ_291052,RMVar_hsa_circ_310236,RMVar_hsa_circ_218158,RMVar_hsa_circ_218157,RMVar_hsa_circ_372667 29477 RMVar_ID_29477 Human_SNP_ID_132490063 A-to-I Human chr3 - 49337239 49337239 49337239 GGTTTTATTCCTGTCACCCAGGCTAGAGTGCAATGGCATGATCTCAGCTCACTGCAACTTCTGTC GGTTTTATTCCTGTCACCCAGGCTAGAGTGCAGTGGCATGATCTCAGCTCACTGCAACTTCTGTC T C USP4 Ensembl:ENSG00000114316 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs35567703 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99739,RMVar_hsa_circ_218141 29478 RMVar_ID_29478 Human_SNP_ID_132496599 A-to-I Human chr3 - 49359890 49359890 49359890 GAAAGAGAAACAGTTGGTAACTTTTGTGAATTAGGCTGTAACTACTTTATAACTAACATGTCCTG GAAAGAGAAACAGTTGGTAACTTTTGTGAATTGGGCTGTAACTACTTTATAACTAACATGTCCTG T C RHOA Ensembl:ENSG00000067560 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs11552764 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_604190,Human_RBP_ID_1033632,Human_RBP_ID_1205792,Human_RBP_ID_1628540,Human_RBP_ID_1964623,Human_RBP_ID_2789154,Human_RBP_ID_3710305,Human_RBP_ID_5207703,Human_RBP_ID_7204763,Human_RBP_ID_8209727,Human_RBP_ID_8574891,Human_RBP_ID_9141459,Human_RBP_ID_14866374,Human_RBP_ID_17290488,Human_RBP_ID_17403795,Human_RBP_ID_17520309,Human_RBP_ID_18182126,Human_RBP_ID_18339332,Human_RBP_ID_18810466,Human_RBP_ID_22398679,Human_RBP_ID_22457334,Human_RBP_ID_22824185,Human_RBP_ID_23213150,Human_RBP_ID_24007924,Human_RBP_ID_24427995,Human_RBP_ID_24498345,Human_RBP_ID_26508438,Human_RBP_ID_27719304 Human_miRNA_ID_2062416,Human_miRNA_ID_2447962,Human_miRNA_ID_2900086 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_218169,RMVar_hsa_circ_218162 29479 RMVar_ID_29479 Human_SNP_ID_132496810 A-to-I Human chr3 - 49360596 49360596 49360596 GGGCGTGGTGGTGGGCACCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCGGGAGAATCCCTTGAA GGGCGTGGTGGTGGGCACCTGTAGTCCCAGCTTCTCGGGAGGCTGAGGCGGGAGAATCCCTTGAA T A RHOA Ensembl:ENSG00000067560 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1424842946 Functional Loss SNV dbSNP153 33..33 33 - - - 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 29480 RMVar_ID_29480 Human_SNP_ID_132496813 A-to-I Human chr3 - 49360606 49360606 49360606 AAAATTACTTGGGCGTGGTGGTGGGCACCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCGGGAGA AAAATTACTTGGGCGTGGTGGTGGGCACCTGTGGTCCCAGCTACTCGGGAGGCTGAGGCGGGAGA T C RHOA Ensembl:ENSG00000067560 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1426202601 Functional Loss SNV dbSNP153 33..33 33 - - - 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 29481 RMVar_ID_29481 Human_SNP_ID_132496904 A-to-I Human chr3 - 49360961 49360960 49360961 TTAAGCGATTCCCCTGCCTCAGCCTCCTGAGTAGCTGGGGTTACAGGCGCCCACTACCACACCCA TTAAGCGATTCCCCTGCCTCAGCCTCCTGAGT_GCTGGGGTTACAGGCGCCCACTACCACACCCA CT C RHOA Ensembl:ENSG00000067560 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1305561427 Functional Loss DEL dbSNP153 33..33 33 - - - Human_Splice_Rec_428987 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 29482 RMVar_ID_29482 Human_SNP_ID_132496923 A-to-I Human chr3 - 49360990 49360989 49360990 GGCTCAACTGCAACCTCCGCCTCCCAGATTTAAGCGATTCCCCTGCCTCAGCCTCCTGAGTAGCT GGCTCAACTGCAACCTCCGCCTCCCAGATTTA_GCGATTCCCCTGCCTCAGCCTCCTGAGTAGCT CT C RHOA Ensembl:ENSG00000067560 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1424315230 Functional Loss DEL dbSNP153 33..33 33 - - - Human_Splice_Rec_428987 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 29483 RMVar_ID_29483 Human_SNP_ID_132496927 A-to-I Human chr3 - 49360997 49360997 49360997 CGATCTTGGCTCAACTGCAACCTCCGCCTCCCAGATTTAAGCGATTCCCCTGCCTCAGCCTCCTG CGATCTTGGCTCAACTGCAACCTCCGCCTCCCGGATTTAAGCGATTCCCCTGCCTCAGCCTCCTG T C RHOA Ensembl:ENSG00000067560 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1310116062 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14866425 Human_Splice_Rec_428987 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 29484 RMVar_ID_29484 Human_SNP_ID_132497528 A-to-I Human chr3 - 49363229 49363229 49363229 TATTTTTAGTAGAGACGGGGTTTCACTGTGTTAGCCAGGATGGTCTCGATCTCCTGACCTCATGA TATTTTTAGTAGAGACGGGGTTTCACTGTGTTGGCCAGGATGGTCTCGATCTCCTGACCTCATGA T C RHOA Ensembl:ENSG00000067560 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1482961915 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91759,RMVar_hsa_circ_126650,RMVar_hsa_circ_90043,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_218172,RMVar_hsa_circ_124898,RMVar_hsa_circ_300766,RMVar_hsa_circ_295148,RMVar_hsa_circ_82726,RMVar_hsa_circ_218171 29485 RMVar_ID_29485 Human_SNP_ID_132498142 A-to-I Human chr3 - 49365372 49365372 49365372 TTGGGAGGCCAAGGTGGGTGGATCCTGAGGTCAGGAGTTCAAGACCAGCCTGTCCAACATGGTGA TTGGGAGGCCAAGGTGGGTGGATCCTGAGGTCGGGAGTTCAAGACCAGCCTGTCCAACATGGTGA T C RHOA,RHOA-IT1 Ensembl:ENSG00000067560,Ensembl:ENSG00000235908 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs953805007 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91759,RMVar_hsa_circ_126650,RMVar_hsa_circ_90043,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_218172,RMVar_hsa_circ_124898,RMVar_hsa_circ_300766,RMVar_hsa_circ_295148,RMVar_hsa_circ_82726,RMVar_hsa_circ_218171 29486 RMVar_ID_29486 Human_SNP_ID_132498430 A-to-I Human chr3 - 49366411 49366411 49366411 TTTAGTAGAGACCGGGTTTCTCCGTGTTGGCCAGGCTTCTCTCAAACTTCTGACCTCTGGTGATC TTTAGTAGAGACCGGGTTTCTCCGTGTTGGCCGGGCTTCTCTCAAACTTCTGACCTCTGGTGATC T C RHOA,RHOA-IT1 Ensembl:ENSG00000067560,Ensembl:ENSG00000235908 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1429075720 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14866576 RMVar_hsa_circ_91759,RMVar_hsa_circ_126650,RMVar_hsa_circ_90043,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_218172,RMVar_hsa_circ_124898,RMVar_hsa_circ_300766,RMVar_hsa_circ_295148,RMVar_hsa_circ_82726,RMVar_hsa_circ_218171 29487 RMVar_ID_29487 Human_SNP_ID_132498441 A-to-I Human chr3 - 49366437 49366437 49366437 CCCCACGCCTGGGTGATTTTTGTATTTTTAGTAGAGACCGGGTTTCTCCGTGTTGGCCAGGCTTC CCCCACGCCTGGGTGATTTTTGTATTTTTAGTGGAGACCGGGTTTCTCCGTGTTGGCCAGGCTTC T C RHOA,RHOA-IT1 Ensembl:ENSG00000067560,Ensembl:ENSG00000235908 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1001172112 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91759,RMVar_hsa_circ_126650,RMVar_hsa_circ_90043,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_218172,RMVar_hsa_circ_124898,RMVar_hsa_circ_300766,RMVar_hsa_circ_295148,RMVar_hsa_circ_82726,RMVar_hsa_circ_218171 29488 RMVar_ID_29488 Human_SNP_ID_132498443 A-to-I Human chr3 - 49366440 49366440 49366440 CGCCCCCACGCCTGGGTGATTTTTGTATTTTTAGTAGAGACCGGGTTTCTCCGTGTTGGCCAGGC CGCCCCCACGCCTGGGTGATTTTTGTATTTTTGGTAGAGACCGGGTTTCTCCGTGTTGGCCAGGC T C RHOA,RHOA-IT1 Ensembl:ENSG00000067560,Ensembl:ENSG00000235908 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs780398237 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91759,RMVar_hsa_circ_126650,RMVar_hsa_circ_90043,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_218172,RMVar_hsa_circ_124898,RMVar_hsa_circ_300766,RMVar_hsa_circ_295148,RMVar_hsa_circ_82726,RMVar_hsa_circ_218171 29489 RMVar_ID_29489 Human_SNP_ID_132498622 A-to-I Human chr3 - 49367153 49367153 49367153 ATTTTTTAGTAGAGATGGGATTTCACCACGTTAGCCAGGATGATCTTGATCTCCTGACCTCGTGA ATTTTTTAGTAGAGATGGGATTTCACCACGTTGGCCAGGATGATCTTGATCTCCTGACCTCGTGA T C RHOA Ensembl:ENSG00000067560 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1012235530 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91759,RMVar_hsa_circ_126650,RMVar_hsa_circ_90043,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_218172,RMVar_hsa_circ_124898,RMVar_hsa_circ_300766,RMVar_hsa_circ_295148,RMVar_hsa_circ_82726,RMVar_hsa_circ_218171 29490 RMVar_ID_29490 Human_SNP_ID_132498873 A-to-I Human chr3 - 49367972 49367972 49367972 CTGGTAGGTGGAGATTGCAGTGAGCCGAGATTATGGCACTGCATTCCAGACTGAGCAACAGAGCA CTGGTAGGTGGAGATTGCAGTGAGCCGAGATTGTGGCACTGCATTCCAGACTGAGCAACAGAGCA T C RHOA Ensembl:ENSG00000067560 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs181064919 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91759,RMVar_hsa_circ_126650,RMVar_hsa_circ_90043,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_218172,RMVar_hsa_circ_124898,RMVar_hsa_circ_300766,RMVar_hsa_circ_295148,RMVar_hsa_circ_82726,RMVar_hsa_circ_218171 29491 RMVar_ID_29491 Human_SNP_ID_132498909 A-to-I Human chr3 - 49368113 49368113 49368113 AGGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCCCGTCTTTACTAAAAGTACAAA AGGGTCAGGAGTTCAAGACCAGCCTGGCCAACGTGGTGAAACCCCGTCTTTACTAAAAGTACAAA T C RHOA Ensembl:ENSG00000067560 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1466309660 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91759,RMVar_hsa_circ_126650,RMVar_hsa_circ_90043,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_218172,RMVar_hsa_circ_124898,RMVar_hsa_circ_300766,RMVar_hsa_circ_295148,RMVar_hsa_circ_82726,RMVar_hsa_circ_218171 29492 RMVar_ID_29492 Human_SNP_ID_132498910 A-to-I Human chr3 - 49368115 49368115 49368115 TGAGGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCCCGTCTTTACTAAAAGTACA TGAGGGTCAGGAGTTCAAGACCAGCCTGGCCAGCATGGTGAAACCCCGTCTTTACTAAAAGTACA T C RHOA Ensembl:ENSG00000067560 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs555461432 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91759,RMVar_hsa_circ_126650,RMVar_hsa_circ_90043,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_218172,RMVar_hsa_circ_124898,RMVar_hsa_circ_300766,RMVar_hsa_circ_295148,RMVar_hsa_circ_82726,RMVar_hsa_circ_218171 29493 RMVar_ID_29493 Human_SNP_ID_132498915 A-to-I Human chr3 - 49368131 49368131 49368131 AGACGGGTGGATCACCTGAGGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCCCGT AGACGGGTGGATCACCTGAGGGTCAGGAGTTCTAGACCAGCCTGGCCAACATGGTGAAACCCCGT T A RHOA Ensembl:ENSG00000067560 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1191293202 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91759,RMVar_hsa_circ_126650,RMVar_hsa_circ_90043,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_218172,RMVar_hsa_circ_124898,RMVar_hsa_circ_300766,RMVar_hsa_circ_295148,RMVar_hsa_circ_82726,RMVar_hsa_circ_218171 29494 RMVar_ID_29494 Human_SNP_ID_132499394 A-to-I Human chr3 - 49369476 49369476 49369476 AGCCCGCCTCAGCCTCCCAAAGTGCTAGGATTACAGGCATGAGCCACCGCGCCTGGCCACACTCA AGCCCGCCTCAGCCTCCCAAAGTGCTAGGATTGCAGGCATGAGCCACCGCGCCTGGCCACACTCA T C RHOA Ensembl:ENSG00000067560 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1272296757 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91759,RMVar_hsa_circ_126650,RMVar_hsa_circ_90043,RMVar_hsa_circ_84516,RMVar_hsa_circ_218165,RMVar_hsa_circ_218167,RMVar_hsa_circ_218168,RMVar_hsa_circ_218166,RMVar_hsa_circ_218172,RMVar_hsa_circ_124898,RMVar_hsa_circ_82726,RMVar_hsa_circ_218174,RMVar_hsa_circ_218176,RMVar_hsa_circ_298357,RMVar_hsa_circ_218171,RMVar_hsa_circ_218175 29495 RMVar_ID_29495 Human_SNP_ID_132499467 A-to-I Human chr3 - 49369648 49369648 49369648 TCACTGCAACCTTTGCCTCTCGAGTTCAAGCAATTCACCTGCCTTAGCCTCTCCAGTAGCTGGGA TCACTGCAACCTTTGCCTCTCGAGTTCAAGCAGTTCACCTGCCTTAGCCTCTCCAGTAGCTGGGA T C RHOA Ensembl:ENSG00000067560 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1216244451 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14866621 RMVar_hsa_circ_91759,RMVar_hsa_circ_126650,RMVar_hsa_circ_90043,RMVar_hsa_circ_84516,RMVar_hsa_circ_218165,RMVar_hsa_circ_218167,RMVar_hsa_circ_218168,RMVar_hsa_circ_218166,RMVar_hsa_circ_218172,RMVar_hsa_circ_124898,RMVar_hsa_circ_82726,RMVar_hsa_circ_218174,RMVar_hsa_circ_218176,RMVar_hsa_circ_298357,RMVar_hsa_circ_218171,RMVar_hsa_circ_218175 29496 RMVar_ID_29496 Human_SNP_ID_132499918 A-to-I Human chr3 - 49371508 49371508 49371508 GGGAGGCTGAGGCAGGAGGATCACCAGAGGTCAGGAGTTTGAGACCAGCCTGCCCAACATGGCAA GGGAGGCTGAGGCAGGAGGATCACCAGAGGTCTGGAGTTTGAGACCAGCCTGCCCAACATGGCAA T A RHOA Ensembl:ENSG00000067560 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs762457408 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14866656 RMVar_hsa_circ_91759,RMVar_hsa_circ_126650,RMVar_hsa_circ_90043,RMVar_hsa_circ_84516,RMVar_hsa_circ_218165,RMVar_hsa_circ_218167,RMVar_hsa_circ_218168,RMVar_hsa_circ_218166,RMVar_hsa_circ_218172,RMVar_hsa_circ_124898,RMVar_hsa_circ_82726,RMVar_hsa_circ_218174,RMVar_hsa_circ_218176,RMVar_hsa_circ_298357,RMVar_hsa_circ_218171,RMVar_hsa_circ_218175 29497 RMVar_ID_29497 Human_SNP_ID_132500325 A-to-I Human chr3 - 49373081 49373081 49373081 CCTTGGCCTCCCAAAGTGCTGGGATTACATGCATGAGCCACCGTGCCTGGCCACTTCTACTTGTC CCTTGGCCTCCCAAAGTGCTGGGATTACATGCGTGAGCCACCGTGCCTGGCCACTTCTACTTGTC T C RHOA Ensembl:ENSG00000067560 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1187195856 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91759,RMVar_hsa_circ_126650,RMVar_hsa_circ_90043,RMVar_hsa_circ_84516,RMVar_hsa_circ_218165,RMVar_hsa_circ_218167,RMVar_hsa_circ_218168,RMVar_hsa_circ_218166,RMVar_hsa_circ_218172,RMVar_hsa_circ_124898,RMVar_hsa_circ_82726,RMVar_hsa_circ_218174,RMVar_hsa_circ_218176,RMVar_hsa_circ_298357,RMVar_hsa_circ_218171,RMVar_hsa_circ_218175 29498 RMVar_ID_29498 Human_SNP_ID_132500377 A-to-I Human chr3 - 49373257 49373257 49373257 TTACAACAACCTCCGCCTCCTGAGTTCAAGCAATTCTCCTATCTCAGCCTCCCGAGGAGCTGGGA TTACAACAACCTCCGCCTCCTGAGTTCAAGCAGTTCTCCTATCTCAGCCTCCCGAGGAGCTGGGA T C RHOA Ensembl:ENSG00000067560 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1429434020 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_429000 RMVar_hsa_circ_91759,RMVar_hsa_circ_126650,RMVar_hsa_circ_90043,RMVar_hsa_circ_84516,RMVar_hsa_circ_218165,RMVar_hsa_circ_218167,RMVar_hsa_circ_218168,RMVar_hsa_circ_218166,RMVar_hsa_circ_218172,RMVar_hsa_circ_124898,RMVar_hsa_circ_82726,RMVar_hsa_circ_218174,RMVar_hsa_circ_218176,RMVar_hsa_circ_298357,RMVar_hsa_circ_218171,RMVar_hsa_circ_218175 29499 RMVar_ID_29499 Human_SNP_ID_132500759 A-to-I Human chr3 - 49374675 49374675 49374675 CTCTGTCGCCCAGGCTGGAGTGCAGTGGTACAATCTCAGCTCGCTGCAACCTCCACCTCCCGGGT CTCTGTCGCCCAGGCTGGAGTGCAGTGGTACAGTCTCAGCTCGCTGCAACCTCCACCTCCCGGGT T C RHOA Ensembl:ENSG00000067560 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs551143851 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91759,RMVar_hsa_circ_126650,RMVar_hsa_circ_90043,RMVar_hsa_circ_84516,RMVar_hsa_circ_218165,RMVar_hsa_circ_218167,RMVar_hsa_circ_218168,RMVar_hsa_circ_218166,RMVar_hsa_circ_218172,RMVar_hsa_circ_124898,RMVar_hsa_circ_82726,RMVar_hsa_circ_218176,RMVar_hsa_circ_298357,RMVar_hsa_circ_218171 29500 RMVar_ID_29500 Human_SNP_ID_132501910 A-to-I Human chr3 - 49378675 49378675 49378675 CGCTTGAGTTGAGCCTGGGAGGCAGAGGCTGCAGTGAGCCAATATTGCACCACTGCATTCCAGCC CGCTTGAGTTGAGCCTGGGAGGCAGAGGCTGCGGTGAGCCAATATTGCACCACTGCATTCCAGCC T C RHOA Ensembl:ENSG00000067560 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1438822542 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91759,RMVar_hsa_circ_126650,RMVar_hsa_circ_218167,RMVar_hsa_circ_218168,RMVar_hsa_circ_218172,RMVar_hsa_circ_124898,RMVar_hsa_circ_82726,RMVar_hsa_circ_218171 29501 RMVar_ID_29501 Human_SNP_ID_132501928 A-to-I Human chr3 - 49378742 49378742 49378742 AAATTAGTCAGCTGTGGTGGCAGGAGCCTGGTAGTCCCAGCTACTGGAGAGGTTGAGGTGGGAGG AAATTAGTCAGCTGTGGTGGCAGGAGCCTGGTCGTCCCAGCTACTGGAGAGGTTGAGGTGGGAGG T G RHOA Ensembl:ENSG00000067560 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs760812313 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25742276 RMVar_hsa_circ_91759,RMVar_hsa_circ_126650,RMVar_hsa_circ_218167,RMVar_hsa_circ_218168,RMVar_hsa_circ_218172,RMVar_hsa_circ_124898,RMVar_hsa_circ_82726,RMVar_hsa_circ_218171 29502 RMVar_ID_29502 Human_SNP_ID_132505005 A-to-I Human chr3 - 49389276 49389276 49389276 GAGTCTCGCTTTGTCGCCCAGGCTGGAGCGCAATGTCACAATCTTCACTCACTGCAAGCTCAGCC GAGTCTCGCTTTGTCGCCCAGGCTGGAGCGCAGTGTCACAATCTTCACTCACTGCAAGCTCAGCC T C RHOA Ensembl:ENSG00000067560 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs184372302 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91759,RMVar_hsa_circ_126650,RMVar_hsa_circ_218167,RMVar_hsa_circ_218168,RMVar_hsa_circ_218172,RMVar_hsa_circ_124898,RMVar_hsa_circ_82726,RMVar_hsa_circ_218171 29503 RMVar_ID_29503 Human_SNP_ID_132505747 A-to-I Human chr3 - 49391649 49391649 49391649 AAATTACCCGGGCATGGTGGTGCATGCCTGTAATCCCAGCTACCGGGGAGGCGGAGGTTGTAGTG AAATTACCCGGGCATGGTGGTGCATGCCTGTAGTCCCAGCTACCGGGGAGGCGGAGGTTGTAGTG T C RHOA Ensembl:ENSG00000067560 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs995993328 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91759,RMVar_hsa_circ_126650,RMVar_hsa_circ_218167,RMVar_hsa_circ_218168,RMVar_hsa_circ_218172,RMVar_hsa_circ_124898,RMVar_hsa_circ_82726,RMVar_hsa_circ_218171 29504 RMVar_ID_29504 Human_SNP_ID_132505998 A-to-I Human chr3 - 49392403 49392403 49392403 GGGACTCACTCTGGCACCCAGGCTGGAGAGCAATGGTATGATCATGGCTCACTGTAGACTTTACC GGGACTCACTCTGGCACCCAGGCTGGAGAGCAGTGGTATGATCATGGCTCACTGTAGACTTTACC T C RHOA Ensembl:ENSG00000067560 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs975080244 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91759,RMVar_hsa_circ_126650,RMVar_hsa_circ_218167,RMVar_hsa_circ_218168,RMVar_hsa_circ_218172,RMVar_hsa_circ_124898,RMVar_hsa_circ_82726,RMVar_hsa_circ_218171 29505 RMVar_ID_29505 Human_SNP_ID_132506275 A-to-I Human chr3 - 49393496 49393496 49393496 CCCAGGAGTTGGAGACCCGTCTGGCCCATATGATGGAACCCCATCTCTACAGCAATTAGCCAAAC CCCAGGAGTTGGAGACCCGTCTGGCCCATATGGTGGAACCCCATCTCTACAGCAATTAGCCAAAC T C RHOA Ensembl:ENSG00000067560 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs895576294 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91759,RMVar_hsa_circ_126650,RMVar_hsa_circ_218167,RMVar_hsa_circ_218168,RMVar_hsa_circ_218172,RMVar_hsa_circ_124898,RMVar_hsa_circ_82726,RMVar_hsa_circ_218171 29506 RMVar_ID_29506 Human_SNP_ID_132506299 A-to-I Human chr3 - 49393577 49393577 49393577 AAAAAAAAAAAAAAGCCAGTGCAGTGGCCTACACCTGTAATCTGAGCACTTTGGGAGGCCAAGGC AAAAAAAAAAAAAAGCCAGTGCAGTGGCCTACGCCTGTAATCTGAGCACTTTGGGAGGCCAAGGC T C RHOA Ensembl:ENSG00000067560 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1160071105 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91759,RMVar_hsa_circ_126650,RMVar_hsa_circ_218167,RMVar_hsa_circ_218168,RMVar_hsa_circ_218172,RMVar_hsa_circ_124898,RMVar_hsa_circ_82726,RMVar_hsa_circ_218171 29507 RMVar_ID_29507 Human_SNP_ID_132506493 A-to-I Human chr3 - 49393762 49393762 49393762 GAGGTTGCAGTGAGCCGAGATTGCACCACTGCACTCCAGCCTGGGCGACAGAGCGAGATTCTGTC GAGGTTGCAGTGAGCCGAGATTGCACCACTGCCCTCCAGCCTGGGCGACAGAGCGAGATTCTGTC T G RHOA Ensembl:ENSG00000067560 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1245625394 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91759,RMVar_hsa_circ_126650,RMVar_hsa_circ_218167,RMVar_hsa_circ_218168,RMVar_hsa_circ_218172,RMVar_hsa_circ_124898,RMVar_hsa_circ_82726,RMVar_hsa_circ_218171 29508 RMVar_ID_29508 Human_SNP_ID_132506676 A-to-I Human chr3 - 49394419 49394419 49394419 TGGAACCCGGGAGGTGGAGGTTGCATTGAGCCAAGATCATGCCACTGCACTTCAGCCTGGGCAAC TGGAACCCGGGAGGTGGAGGTTGCATTGAGCCGAGATCATGCCACTGCACTTCAGCCTGGGCAAC T C RHOA Ensembl:ENSG00000067560 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1456998476 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23312690 RMVar_hsa_circ_91759,RMVar_hsa_circ_126650,RMVar_hsa_circ_218167,RMVar_hsa_circ_218168,RMVar_hsa_circ_218172,RMVar_hsa_circ_124898,RMVar_hsa_circ_82726,RMVar_hsa_circ_218171 29509 RMVar_ID_29509 Human_SNP_ID_132506687 A-to-I Human chr3 - 49394475 49394475 49394475 ATGGTTGTGCGCACCTGTAATTCTAGTTACTCATGAGGCTGATGCAGGAGAATTGGTGGAACCCG ATGGTTGTGCGCACCTGTAATTCTAGTTACTCGTGAGGCTGATGCAGGAGAATTGGTGGAACCCG T C RHOA Ensembl:ENSG00000067560 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1253932665 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91759,RMVar_hsa_circ_126650,RMVar_hsa_circ_218167,RMVar_hsa_circ_218168,RMVar_hsa_circ_218172,RMVar_hsa_circ_124898,RMVar_hsa_circ_82726,RMVar_hsa_circ_218171 29510 RMVar_ID_29510 Human_SNP_ID_132506690 A-to-I Human chr3 - 49394488 49394488 49394488 AAATTAGCTGGGCATGGTTGTGCGCACCTGTAATTCTAGTTACTCATGAGGCTGATGCAGGAGAA AAATTAGCTGGGCATGGTTGTGCGCACCTGTAGTTCTAGTTACTCATGAGGCTGATGCAGGAGAA T C RHOA Ensembl:ENSG00000067560 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs535236748 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91759,RMVar_hsa_circ_126650,RMVar_hsa_circ_218167,RMVar_hsa_circ_218168,RMVar_hsa_circ_218172,RMVar_hsa_circ_124898,RMVar_hsa_circ_82726,RMVar_hsa_circ_218171 29511 RMVar_ID_29511 Human_SNP_ID_132507310 A-to-I Human chr3 - 49396607 49396607 49396607 CACCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGACGTGTG CACCTCCCAGGTTCAAGCGATTCTCCTGCCTCGGCCTCCCGAGTAGCTGGGATTACAGACGTGTG T C RHOA Ensembl:ENSG00000067560 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1313936406 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91759,RMVar_hsa_circ_126650,RMVar_hsa_circ_218167,RMVar_hsa_circ_218168,RMVar_hsa_circ_218172,RMVar_hsa_circ_124898,RMVar_hsa_circ_82726,RMVar_hsa_circ_218171 29512 RMVar_ID_29512 Human_SNP_ID_132509863 A-to-I Human chr3 - 49404401 49404401 49404401 TTTACTAGAGACGGGGTTTTACTTTGTTGGCCAGGCTGGTCTTGAACTCCTGACCTTGTGATCCA TTTACTAGAGACGGGGTTTTACTTTGTTGGCCCGGCTGGTCTTGAACTCCTGACCTTGTGATCCA T G RHOA Ensembl:ENSG00000067560 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167980867 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91759,RMVar_hsa_circ_126650,RMVar_hsa_circ_218167,RMVar_hsa_circ_218168,RMVar_hsa_circ_218172,RMVar_hsa_circ_124898,RMVar_hsa_circ_82726,RMVar_hsa_circ_218171 29513 RMVar_ID_29513 Human_SNP_ID_132509964 A-to-I Human chr3 - 49404511 49404511 49404511 GCCTACCAGGGTGCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGTGCGTG GCCTACCAGGGTGCAAGCGATTCTCCTGCCTCTGCCTCCCAAGTAGCTGGGACTACAGGTGCGTG T A RHOA Ensembl:ENSG00000067560 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1287627448 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91759,RMVar_hsa_circ_126650,RMVar_hsa_circ_218167,RMVar_hsa_circ_218168,RMVar_hsa_circ_218172,RMVar_hsa_circ_124898,RMVar_hsa_circ_82726,RMVar_hsa_circ_218171 29514 RMVar_ID_29514 Human_SNP_ID_132510445 A-to-I Human chr3 - 49405813 49405813 49405813 GAGTGTATTAGTGAGTGCCTGTAATCCCAGCTACTCGGAAGGCTGAAGCAGGAGAATCCCTCGAA GAGTGTATTAGTGAGTGCCTGTAATCCCAGCTGCTCGGAAGGCTGAAGCAGGAGAATCCCTCGAA T C RHOA Ensembl:ENSG00000067560 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1292638997 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91759,RMVar_hsa_circ_126650,RMVar_hsa_circ_218167,RMVar_hsa_circ_218168,RMVar_hsa_circ_218172,RMVar_hsa_circ_124898,RMVar_hsa_circ_82726,RMVar_hsa_circ_218171 29515 RMVar_ID_29515 Human_SNP_ID_132510813 A-to-I Human chr3 - 49407064 49407064 49407064 TTGTTCACTTCAACCTTTGTTTCCCAGGTTCAAGCGATTCTCGTGCCTCAGTCTCTAGAGTAGCT TTGTTCACTTCAACCTTTGTTTCCCAGGTTCATGCGATTCTCGTGCCTCAGTCTCTAGAGTAGCT T A RHOA Ensembl:ENSG00000067560 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs150752628 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91759,RMVar_hsa_circ_126650,RMVar_hsa_circ_218167,RMVar_hsa_circ_218168,RMVar_hsa_circ_218172,RMVar_hsa_circ_124898,RMVar_hsa_circ_82726,RMVar_hsa_circ_218171 29516 RMVar_ID_29516 Human_SNP_ID_132510814 A-to-I Human chr3 - 49407064 49407064 49407064 TTGTTCACTTCAACCTTTGTTTCCCAGGTTCAAGCGATTCTCGTGCCTCAGTCTCTAGAGTAGCT TTGTTCACTTCAACCTTTGTTTCCCAGGTTCAGGCGATTCTCGTGCCTCAGTCTCTAGAGTAGCT T C RHOA Ensembl:ENSG00000067560 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs150752628 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91759,RMVar_hsa_circ_126650,RMVar_hsa_circ_218167,RMVar_hsa_circ_218168,RMVar_hsa_circ_218172,RMVar_hsa_circ_124898,RMVar_hsa_circ_82726,RMVar_hsa_circ_218171 29517 RMVar_ID_29517 Human_SNP_ID_132510964 A-to-I Human chr3 - 49407417 49407417 49407417 CCAGCCTGGCCACATGGTGAAACCCTGTCTCTACTAAAAATACAAAACATTAGCTGGGCGTGGCA CCAGCCTGGCCACATGGTGAAACCCTGTCTCTGCTAAAAATACAAAACATTAGCTGGGCGTGGCA T C RHOA Ensembl:ENSG00000067560 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1177565624 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91759,RMVar_hsa_circ_126650,RMVar_hsa_circ_218167,RMVar_hsa_circ_218168,RMVar_hsa_circ_218172,RMVar_hsa_circ_124898,RMVar_hsa_circ_82726,RMVar_hsa_circ_218171 29518 RMVar_ID_29518 Human_SNP_ID_132511120 A-to-I Human chr3 - 49407994 49407994 49407994 CACTGTGCTCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGTCAGGCTGT CACTGTGCTCAGCTAATTTTTGTATTTTTAGTGGAGACGGGGTTTCACCATGTTGGTCAGGCTGT T C RHOA Ensembl:ENSG00000067560 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1183656797 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91759,RMVar_hsa_circ_126650,RMVar_hsa_circ_218167,RMVar_hsa_circ_218168,RMVar_hsa_circ_218172,RMVar_hsa_circ_124898,RMVar_hsa_circ_82726,RMVar_hsa_circ_218171 29519 RMVar_ID_29519 Human_SNP_ID_132511122 A-to-I Human chr3 - 49407997 49407997 49407997 CGCCACTGTGCTCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGTCAGGC CGCCACTGTGCTCAGCTAATTTTTGTATTTTTGGTAGAGACGGGGTTTCACCATGTTGGTCAGGC T C RHOA Ensembl:ENSG00000067560 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1293907027 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91759,RMVar_hsa_circ_126650,RMVar_hsa_circ_218167,RMVar_hsa_circ_218168,RMVar_hsa_circ_218172,RMVar_hsa_circ_124898,RMVar_hsa_circ_82726,RMVar_hsa_circ_218171 29520 RMVar_ID_29520 Human_SNP_ID_132511160 A-to-I Human chr3 - 49408118 49408118 49408118 GTCTCACTCTGTCGTCCGGGCCAGAGTGCAGTAGCGCCATCTCGGCTCACTGCAACCGCCGCCTC GTCTCACTCTGTCGTCCGGGCCAGAGTGCAGTTGCGCCATCTCGGCTCACTGCAACCGCCGCCTC T A RHOA Ensembl:ENSG00000067560 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1175636981 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14867488,Human_RBP_ID_24382989 RMVar_hsa_circ_91759,RMVar_hsa_circ_126650,RMVar_hsa_circ_218167,RMVar_hsa_circ_218168,RMVar_hsa_circ_218172,RMVar_hsa_circ_124898,RMVar_hsa_circ_82726,RMVar_hsa_circ_218171 29521 RMVar_ID_29521 Human_SNP_ID_132513447 A-to-I Human chr3 + 49415261 49415261 49415261 TGAGTTGGCCAGGCATGGTGGCTCACGCCTGTAATCCCAACACTTTGGGAGGCTGAGGCAGGCAG TGAGTTGGCCAGGCATGGTGGCTCACGCCTGTCATCCCAACACTTTGGGAGGCTGAGGCAGGCAG A C TCTA Ensembl:ENSG00000145022 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1270339806 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_218177,RMVar_hsa_circ_107323,RMVar_hsa_circ_117505,RMVar_hsa_circ_218178 29522 RMVar_ID_29522 Human_SNP_ID_132513492 A-to-I Human chr3 + 49415465 49415465 49415465 TTGAACCTGGGAGGCAGAGGTTGCAGTGAGCCAAGATTGCGCCGTTGTACTCCAGCCTGGGCAAC TTGAACCTGGGAGGCAGAGGTTGCAGTGAGCCGAGATTGCGCCGTTGTACTCCAGCCTGGGCAAC A G TCTA Ensembl:ENSG00000145022 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1425899476 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_218177,RMVar_hsa_circ_107323,RMVar_hsa_circ_117505,RMVar_hsa_circ_218178 29523 RMVar_ID_29523 Human_SNP_ID_132515996 A-to-I Human chr3 - 49423500 49423500 49423500 TGCCTGCCTTGGCCTTCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCGCCCGCCCTGCCCCT TGCCTGCCTTGGCCTTCCAAAGTGCTGGGATTCCAGGCATGAGCCACCGCGCCCGCCCTGCCCCT T G NICN1,AC104452.1 Ensembl:ENSG00000145029,Ensembl:ENSG00000283189 Protein coding,Protein coding 3'UTR,3'UTR GSE47997;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 K562 cells&HepG2 cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 23474544,29129909,31158229 RNA-Seq:(High) rs1392158778 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_429828 29524 RMVar_ID_29524 Human_SNP_ID_132516006 A-to-I Human chr3 - 49423550 49423550 49423550 GTTTCTCCATGTTGGTCAGGCTGGTCTCAAACACCTGACCTCAGGTGATCTGCCTGCCTTGGCCT GTTTCTCCATGTTGGTCAGGCTGGTCTCAAACCCCTGACCTCAGGTGATCTGCCTGCCTTGGCCT T G NICN1,AC104452.1 Ensembl:ENSG00000145029,Ensembl:ENSG00000283189 Protein coding,Protein coding 3'UTR,3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1156669352 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_429828 29525 RMVar_ID_29525 Human_SNP_ID_132516018 A-to-I Human chr3 - 49423607 49423607 49423607 GGATTACAGTCATGCATCACCATGCCTGGCTAATTTTGTATTTGTAGTAGAGATGGGGTTTCTCC GGATTACAGTCATGCATCACCATGCCTGGCTAGTTTTGTATTTGTAGTAGAGATGGGGTTTCTCC T C NICN1,AC104452.1 Ensembl:ENSG00000145029,Ensembl:ENSG00000283189 Protein coding,Protein coding 3'UTR,3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs965371588 Functional Loss SNV dbSNP153 33..33 33 - - - 29526 RMVar_ID_29526 Human_SNP_ID_132516042 A-to-I Human chr3 - 49423709 49423709 49423709 TCTTGTTGCCCAGGCTGGAGTGCAATAGTGCAATCTTGGCTAACTGCAACCTCCGCCTCCCAGGT TCTTGTTGCCCAGGCTGGAGTGCAATAGTGCAGTCTTGGCTAACTGCAACCTCCGCCTCCCAGGT T C NICN1,AC104452.1 Ensembl:ENSG00000145029,Ensembl:ENSG00000283189 Protein coding,Protein coding 3'UTR,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs757412226 Functional Loss SNV dbSNP153 33..33 33 - - - 29527 RMVar_ID_29527 Human_SNP_ID_132516097 A-to-I Human chr3 - 49423946 49423946 49423946 ACTTGGGAGGCTGAGGCAGGAGAATCTCTTGAACCCGGGAAGTGGAGGTTGCGGACCTGAGATCA ACTTGGGAGGCTGAGGCAGGAGAATCTCTTGAGCCCGGGAAGTGGAGGTTGCGGACCTGAGATCA T C NICN1,AC104452.1 Ensembl:ENSG00000145029,Ensembl:ENSG00000283189 Protein coding,Protein coding 3'UTR,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1201237019 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17573654,Human_RBP_ID_26510372 29528 RMVar_ID_29528 Human_SNP_ID_132529138 A-to-I Human chr3 + 49473860 49473860 49473860 CCCGCGTCAGCCTCCCAAAGTGTTGAGATTACAGGCGTGAGCCACTGCGCCTGGCCTTTTTTTTT CCCGCGTCAGCCTCCCAAAGTGTTGAGATTACGGGCGTGAGCCACTGCGCCTGGCCTTTTTTTTT A G DAG1 Ensembl:ENSG00000173402 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs960807982 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89210,RMVar_hsa_circ_218182 29529 RMVar_ID_29529 Human_SNP_ID_132529781 A-to-I Human chr3 + 49475843 49475843 49475843 CTCCTGCCTCGGCCTCCCGAGTAGCTGGGACTACAGGTGCCCGCCACCACACCTGGCTAATATAT CTCCTGCCTCGGCCTCCCGAGTAGCTGGGACTGCAGGTGCCCGCCACCACACCTGGCTAATATAT A G DAG1 Ensembl:ENSG00000173402 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs926568002 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89210,RMVar_hsa_circ_218182 29530 RMVar_ID_29530 Human_SNP_ID_132529819 A-to-I Human chr3 + 49475995 49475995 49475995 CCTTGGCCTCCCAAGGTGCTGGGATTACAGGCATGAGCCACTGCACCCGGCCATAGCTAAGCATT CCTTGGCCTCCCAAGGTGCTGGGATTACAGGCGTGAGCCACTGCACCCGGCCATAGCTAAGCATT A G DAG1 Ensembl:ENSG00000173402 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1401040463 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89210,RMVar_hsa_circ_218182 29531 RMVar_ID_29531 Human_SNP_ID_132530105 A-to-I Human chr3 + 49477257 49477257 49477257 GACGTCAGGTGATCTGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGGGTGAGCCACCGCT GACGTCAGGTGATCTGCCCGCCTCGGCCTCCCCAAGTGCTGGGATTACAGGGGTGAGCCACCGCT A C DAG1 Ensembl:ENSG00000173402 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1312385573 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23189662,Human_RBP_ID_25742401 RMVar_hsa_circ_292983,RMVar_hsa_circ_343041,RMVar_hsa_circ_218183 29532 RMVar_ID_29532 Human_SNP_ID_132530106 A-to-I Human chr3 + 49477257 49477257 49477257 GACGTCAGGTGATCTGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGGGTGAGCCACCGCT GACGTCAGGTGATCTGCCCGCCTCGGCCTCCCGAAGTGCTGGGATTACAGGGGTGAGCCACCGCT A G DAG1 Ensembl:ENSG00000173402 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1312385573 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23189662,Human_RBP_ID_25742401 RMVar_hsa_circ_292983,RMVar_hsa_circ_343041,RMVar_hsa_circ_218183 29533 RMVar_ID_29533 Human_SNP_ID_132530148 A-to-I Human chr3 + 49477431 49477431 49477431 CTCCCACCTTGGCCTCCCATGTAGCTGGGACTACAGGGGCATGTCACCATGCCCGGCTAATTTTT CTCCCACCTTGGCCTCCCATGTAGCTGGGACTGCAGGGGCATGTCACCATGCCCGGCTAATTTTT A G DAG1 Ensembl:ENSG00000173402 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277798542 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14868018 RMVar_hsa_circ_292983,RMVar_hsa_circ_343041,RMVar_hsa_circ_218183 29534 RMVar_ID_29534 Human_SNP_ID_132530149 A-to-I Human chr3 + 49477433 49477432 49477433 CCCACCTTGGCCTCCCATGTAGCTGGGACTACAGGGGCATGTCACCATGCCCGGCTAATTTTTGT CCCACCTTGGCCTCCCATGTAGCTGGGACTAC_GGGGCATGTCACCATGCCCGGCTAATTTTTGT CA C DAG1 Ensembl:ENSG00000173402 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1430673697 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_14868018 RMVar_hsa_circ_292983,RMVar_hsa_circ_343041,RMVar_hsa_circ_218183 29535 RMVar_ID_29535 Human_SNP_ID_132530236 A-to-I Human chr3 + 49477752 49477752 49477752 GGGAGGCCGATGTGCACAGATCAACTGAGGTCAGGAGTCTGAGACCAGCCTGGCCAACATGGCGA GGGAGGCCGATGTGCACAGATCAACTGAGGTCTGGAGTCTGAGACCAGCCTGGCCAACATGGCGA A T DAG1 Ensembl:ENSG00000173402 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1382458749 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25742403 RMVar_hsa_circ_292983,RMVar_hsa_circ_343041,RMVar_hsa_circ_218183 29536 RMVar_ID_29536 Human_SNP_ID_132530775 A-to-I Human chr3 + 49479059 49479059 49479059 CTGGTCTCCTGACCTTGTGATCCTCCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG CTGGTCTCCTGACCTTGTGATCCTCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG A G DAG1 Ensembl:ENSG00000173402 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1366364581 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_292983,RMVar_hsa_circ_343041,RMVar_hsa_circ_218183 29537 RMVar_ID_29537 Human_SNP_ID_132534833 A-to-I Human chr3 + 49493312 49493312 49493312 GCAATCCATCAACCTTAGCCTACCAAAGTGCTAGGATTACAGGCATGAACCACTGTGCCTTGCCT GCAATCCATCAACCTTAGCCTACCAAAGTGCTGGGATTACAGGCATGAACCACTGTGCCTTGCCT A G DAG1 Ensembl:ENSG00000173402 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs575724933 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47830,RMVar_hsa_circ_292983,RMVar_hsa_circ_218183 29538 RMVar_ID_29538 Human_SNP_ID_132535739 A-to-I Human chr3 + 49496886 49496886 49496886 TGATCTCGTGATCCACCCACCTCGGCCTCCCAAAGTGTTGGGATTATAGGTGTGAGCCACTATGC TGATCTCGTGATCCACCCACCTCGGCCTCCCACAGTGTTGGGATTATAGGTGTGAGCCACTATGC A C DAG1 Ensembl:ENSG00000173402 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1389151009 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47830,RMVar_hsa_circ_292983,RMVar_hsa_circ_218183 29539 RMVar_ID_29539 Human_SNP_ID_132535743 A-to-I Human chr3 + 49496899 49496899 49496899 CACCCACCTCGGCCTCCCAAAGTGTTGGGATTATAGGTGTGAGCCACTATGCCTGGCCTAAATTT CACCCACCTCGGCCTCCCAAAGTGTTGGGATTGTAGGTGTGAGCCACTATGCCTGGCCTAAATTT A G DAG1 Ensembl:ENSG00000173402 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1010878162 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47830,RMVar_hsa_circ_292983,RMVar_hsa_circ_218183 29540 RMVar_ID_29540 Human_SNP_ID_132535854 A-to-I Human chr3 + 49497362 49497362 49497362 GAGAGGTTGAGGCGAGAGAAGCTCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCCGAGATTGTG GAGAGGTTGAGGCGAGAGAAGCTCTTGAACCCGGGAGGCGGAGGTTGCAGTGAGCCGAGATTGTG A G DAG1 Ensembl:ENSG00000173402 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1336989843 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47830,RMVar_hsa_circ_292983,RMVar_hsa_circ_218183 29541 RMVar_ID_29541 Human_SNP_ID_132538344 A-to-I Human chr3 + 49506854 49506854 49506854 TGAATTGGAGCCAAGTATGGTGGCAAATGCCTATAGTCCTAGCTACTCAGGAGGCTGAGGTGGTG TGAATTGGAGCCAAGTATGGTGGCAAATGCCTCTAGTCCTAGCTACTCAGGAGGCTGAGGTGGTG A C DAG1 Ensembl:ENSG00000173402 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs548976101 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14868783,Human_RBP_ID_25742468 RMVar_hsa_circ_47830,RMVar_hsa_circ_292983,RMVar_hsa_circ_218183 29542 RMVar_ID_29542 Human_SNP_ID_132538345 A-to-I Human chr3 + 49506854 49506854 49506854 TGAATTGGAGCCAAGTATGGTGGCAAATGCCTATAGTCCTAGCTACTCAGGAGGCTGAGGTGGTG TGAATTGGAGCCAAGTATGGTGGCAAATGCCTGTAGTCCTAGCTACTCAGGAGGCTGAGGTGGTG A G DAG1 Ensembl:ENSG00000173402 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs548976101 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14868783,Human_RBP_ID_25742468 RMVar_hsa_circ_47830,RMVar_hsa_circ_292983,RMVar_hsa_circ_218183 29543 RMVar_ID_29543 Human_SNP_ID_132552591 A-to-I Human chr3 + 49564262 49564260 49564262 TCACAGCATGAGAACACCCTTCCTACACCTTTATGAGAGCTTTTGGGCAGCTACTCCCACACTTA TCACAGCATGAGAACACCCTTCCTACACCTT__TGAGAGCTTTTGGGCAGCTACTCCCACACTTA TTA T BSN Ensembl:ENSG00000164061 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs138051624 Functional Loss DEL dbSNP153 32..33 33 - - - 29544 RMVar_ID_29544 Human_SNP_ID_132591619 A-to-I Human chr3 + 49711134 49711134 49711134 TGTAGTCCCAGCTACTCTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGGCGAAACCCCAT TGTAGTCCCAGCTACTCTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGCGAAACCCCAT A G RNF123 Ensembl:ENSG00000164068 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs933791219 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1409,RMVar_hsa_circ_101674,RMVar_hsa_circ_218246,RMVar_hsa_circ_76491,RMVar_hsa_circ_218249,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_114936,RMVar_hsa_circ_117750,RMVar_hsa_circ_218265,RMVar_hsa_circ_82366,RMVar_hsa_circ_218266,RMVar_hsa_circ_218264 29545 RMVar_ID_29545 Human_SNP_ID_132595480 A-to-I Human chr3 - 49722125 49722125 49722125 CCGCTCTCAGGACCCAAGTGCCCGCATCGGCCAGAACTGCAGCATTGGCCCCAATGTGAGCCTGG CCGCTCTCAGGACCCAAGTGCCCGCATCGGCCGGAACTGCAGCATTGGCCCCAATGTGAGCCTGG T C GMPPB Ensembl:ENSG00000173540 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1304295361 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27503154 Human_Splice_Rec_430868,Human_Splice_Rec_430884,Human_Splice_Rec_430900 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 29546 RMVar_ID_29546 Human_SNP_ID_132598365 A-to-I Human chr3 - 49731991 49731991 49731991 TCGAGACTGCAGTGGGCCATGATTGCACCACTACATTCTAGCTTCTAGCCTGGGCAACACAGCAA TCGAGACTGCAGTGGGCCATGATTGCACCACTGCATTCTAGCTTCTAGCCTGGGCAACACAGCAA T C IP6K1 Ensembl:ENSG00000176095 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs938978193 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_218275,RMVar_hsa_circ_82221 29547 RMVar_ID_29547 Human_SNP_ID_132598479 A-to-I Human chr3 - 49732546 49732546 49732546 CTAGAACAGTGTTGTCTGATAGAACTGTCTGTAATTCTGTGTGCTTTTCAGTATGGTAGCCACTG CTAGAACAGTGTTGTCTGATAGAACTGTCTGTCATTCTGTGTGCTTTTCAGTATGGTAGCCACTG T G IP6K1 Ensembl:ENSG00000176095 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1239509488 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3710461,Human_RBP_ID_24008271 RMVar_hsa_circ_218275,RMVar_hsa_circ_82221 29548 RMVar_ID_29548 Human_SNP_ID_132598731 A-to-I Human chr3 - 49733603 49733603 49733603 TAGCAAAATGTTTTCAAGTTCATATATGTTGTAGCATGTATAGGAATTTCATTCCTTTTTATTGC TAGCAAAATGTTTTCAAGTTCATATATGTTGTGGCATGTATAGGAATTTCATTCCTTTTTATTGC T C IP6K1 Ensembl:ENSG00000176095 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1290965570 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_218275,RMVar_hsa_circ_82221,RMVar_hsa_circ_218278 29549 RMVar_ID_29549 Human_SNP_ID_132598733 A-to-I Human chr3 - 49733612 49733612 49733612 TATTTCACTTAGCAAAATGTTTTCAAGTTCATATATGTTGTAGCATGTATAGGAATTTCATTCCT TATTTCACTTAGCAAAATGTTTTCAAGTTCATGTATGTTGTAGCATGTATAGGAATTTCATTCCT T C IP6K1 Ensembl:ENSG00000176095 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1467424310 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_218275,RMVar_hsa_circ_82221,RMVar_hsa_circ_218278 29550 RMVar_ID_29550 Human_SNP_ID_132599404 A-to-I Human chr3 - 49736508 49736506 49736509 ATGCTACAACATGGATGAATCATGAAAACATTATGTTAAATGAAAGAAACCAGACACAAAAGACC ATGCTACAACATGGATGAATCATGAAAACAT___GTTAAATGAAAGAAACCAGACACAAAAGACC CATA C IP6K1 Ensembl:ENSG00000176095 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1418548314 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_218275,RMVar_hsa_circ_82221,RMVar_hsa_circ_218278 29551 RMVar_ID_29551 Human_SNP_ID_132600197 A-to-I Human chr3 - 49739769 49739769 49739769 CTCAGGTGAGGTCCCAGCTACTTGAGAGGCTGAGGCAGGAGGATCACTTGAGTCCAGGAGTTCGA CTCAGGTGAGGTCCCAGCTACTTGAGAGGCTGTGGCAGGAGGATCACTTGAGTCCAGGAGTTCGA T A IP6K1 Ensembl:ENSG00000176095 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs749998048 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_338476 29552 RMVar_ID_29552 Human_SNP_ID_132600405 A-to-I Human chr3 - 49740640 49740640 49740640 ATGCTGTGACACAGATGAACCTTGCAAACACTATGCTAAGTGAACTAAGCCAGACACAAAAGAAC ATGCTGTGACACAGATGAACCTTGCAAACACTGTGCTAAGTGAACTAAGCCAGACACAAAAGAAC T C IP6K1 Ensembl:ENSG00000176095 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs941133366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14870035 RMVar_hsa_circ_338476 29553 RMVar_ID_29553 Human_SNP_ID_132601221 A-to-I Human chr3 - 49743584 49743584 49743584 AAAAAAAAAACTATGGCTCAAGTGATCCTCCCACCTCAGCCCCCCGAGTAGCTGGGACTATAGGC AAAAAAAAAACTATGGCTCAAGTGATCCTCCCCCCTCAGCCCCCCGAGTAGCTGGGACTATAGGC T G IP6K1 Ensembl:ENSG00000176095 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1003121519 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_338476 29554 RMVar_ID_29554 Human_SNP_ID_132601712 A-to-I Human chr3 - 49745537 49745537 49745537 TTTTGTATTTTTAGTAGAGACGGGGTTTTGCCATATTGGCCAGGCTGGTCTCAAACTCAACTCAG TTTTGTATTTTTAGTAGAGACGGGGTTTTGCCGTATTGGCCAGGCTGGTCTCAAACTCAACTCAG T C IP6K1 Ensembl:ENSG00000176095 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1002717668 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_338476 29555 RMVar_ID_29555 Human_SNP_ID_132602970 A-to-I Human chr3 - 49750617 49750617 49750617 CGGCTCACTGAAACCTCTGCCTTCTGGGTTCAAGTGATTCTTGTGCCTCAGCTTCCCAAGTAGCT CGGCTCACTGAAACCTCTGCCTTCTGGGTTCAGGTGATTCTTGTGCCTCAGCTTCCCAAGTAGCT T C IP6K1 Ensembl:ENSG00000176095 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1254455640 Functional Loss SNV dbSNP153 33..33 33 - - - 29556 RMVar_ID_29556 Human_SNP_ID_132606618 A-to-I Human chr3 - 49764696 49764696 49764696 TTTTGTATTTGTAGTAGACATGGGATTGTGCCATGTTGGCCAGGCTGGTCTTGAACTCCCGACCT TTTTGTATTTGTAGTAGACATGGGATTGTGCCGTGTTGGCCAGGCTGGTCTTGAACTCCCGACCT T C IP6K1 Ensembl:ENSG00000176095 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1200856767 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14870751 29557 RMVar_ID_29557 Human_SNP_ID_132606667 A-to-I Human chr3 - 49764876 49764876 49764876 TGGGTTCATTGGGATTCTTTTTTTTTTTTTTCAAGACAGAGTTTCACTCTGTCACCCAGGCTATA TGGGTTCATTGGGATTCTTTTTTTTTTTTTTCCAGACAGAGTTTCACTCTGTCACCCAGGCTATA T G IP6K1 Ensembl:ENSG00000176095 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1030775276 Functional Loss SNV dbSNP153 33..33 33 - - - 29558 RMVar_ID_29558 Human_SNP_ID_132608438 A-to-I Human chr3 - 49771798 49771798 49771798 CATTAACACTACAGTTTGTTTATTCTGTTGATAGATATTTGGGCTGTTTCCAGTGTTTGCCTTAT CATTAACACTACAGTTTGTTTATTCTGTTGATGGATATTTGGGCTGTTTCCAGTGTTTGCCTTAT T C IP6K1 Ensembl:ENSG00000176095 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1209701276 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7205508,Human_RBP_ID_14871099 29559 RMVar_ID_29559 Human_SNP_ID_132608684 A-to-I Human chr3 - 49772460 49772460 49772460 AGATGGAGGCTGCAGTGAATCATGATCGTGCCACTGCACTTTAGCCTGGGTAACAGAGTAAGACC AGATGGAGGCTGCAGTGAATCATGATCGTGCCGCTGCACTTTAGCCTGGGTAACAGAGTAAGACC T C IP6K1 Ensembl:ENSG00000176095 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1248157556 Functional Loss SNV dbSNP153 33..33 33 - - - 29560 RMVar_ID_29560 Human_SNP_ID_132608698 A-to-I Human chr3 - 49772543 49772543 49772543 AAAAAATTAGCTGGGTGTGGCAGCATGTGCCTATAGTCCCAGCTACTAGAGAGGCTGAGATGGGA AAAAAATTAGCTGGGTGTGGCAGCATGTGCCTGTAGTCCCAGCTACTAGAGAGGCTGAGATGGGA T C IP6K1 Ensembl:ENSG00000176095 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs918129074 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_248592 29561 RMVar_ID_29561 Human_SNP_ID_132608778 A-to-I Human chr3 - 49772884 49772884 49772884 AGGAGTTGGAGGCTGCAGTGAGCAGTGATCATACCACTGCACTCCTGCCTGGGTGAGAGTGAGAC AGGAGTTGGAGGCTGCAGTGAGCAGTGATCATGCCACTGCACTCCTGCCTGGGTGAGAGTGAGAC T C IP6K1 Ensembl:ENSG00000176095 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1014589023 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24008347 29562 RMVar_ID_29562 Human_SNP_ID_132608813 A-to-I Human chr3 - 49773043 49773043 49773043 AGGCAGGAGGATCAGTTAAGCTTAGAAGTTCAAAACCAGCCTGGACAACCCAGCAAGGCCCGCTT AGGCAGGAGGATCAGTTAAGCTTAGAAGTTCACAACCAGCCTGGACAACCCAGCAAGGCCCGCTT T G IP6K1 Ensembl:ENSG00000176095 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs925536920 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14871125 29563 RMVar_ID_29563 Human_SNP_ID_132608833 A-to-I Human chr3 - 49773120 49773120 49773120 ATTGGGACTATATACAAAATTATTAATTGGCCAGGTGCAATGGCTCATGCCTGTAATTCCAGCAC ATTGGGACTATATACAAAATTATTAATTGGCCGGGTGCAATGGCTCATGCCTGTAATTCCAGCAC T C IP6K1 Ensembl:ENSG00000176095 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1165089858 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7205513 29564 RMVar_ID_29564 Human_SNP_ID_132609565 A-to-I Human chr3 - 49775512 49775512 49775512 AATCTTTGGGCAGCCATCTCTATCCTTCTCCTAGATGGTGCACTCCTTACAGTAATAGGCACCAG AATCTTTGGGCAGCCATCTCTATCCTTCTCCTGGATGGTGCACTCCTTACAGTAATAGGCACCAG T C IP6K1 Ensembl:ENSG00000176095 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1322140448 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14871256,Human_RBP_ID_18007512 29565 RMVar_ID_29565 Human_SNP_ID_132609569 A-to-I Human chr3 - 49775523 49775523 49775523 CCCAAATTGACAATCTTTGGGCAGCCATCTCTATCCTTCTCCTAGATGGTGCACTCCTTACAGTA CCCAAATTGACAATCTTTGGGCAGCCATCTCTGTCCTTCTCCTAGATGGTGCACTCCTTACAGTA T C IP6K1 Ensembl:ENSG00000176095 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1278356235 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14871256,Human_RBP_ID_17290525,Human_RBP_ID_18007512 29566 RMVar_ID_29566 Human_SNP_ID_132610452 A-to-I Human chr3 - 49778742 49778742 49778742 GCGTGACTGTAACTCCAGCTACTGGGGAGTCTAAGATGGGAGGATCGCTTGTGTCTGGGATTTTG GCGTGACTGTAACTCCAGCTACTGGGGAGTCTCAGATGGGAGGATCGCTTGTGTCTGGGATTTTG T G IP6K1 Ensembl:ENSG00000176095 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388783460 Functional Loss SNV dbSNP153 33..33 33 - - - 29567 RMVar_ID_29567 Human_SNP_ID_132610474 A-to-I Human chr3 - 49778798 49778798 49778798 AACATAGCGAGACCCCATCGATACAAAAAATAAAAAAATTAGCCAGGCGTGGTGGTGCGTGACTG AACATAGCGAGACCCCATCGATACAAAAAATAGAAAAATTAGCCAGGCGTGGTGGTGCGTGACTG T C IP6K1 Ensembl:ENSG00000176095 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1301059943 Functional Loss SNV dbSNP153 33..33 33 - - - 29568 RMVar_ID_29568 Human_SNP_ID_132610613 A-to-I Human chr3 - 49779339 49779339 49779339 ATCAACTGACAGATAAAATGTGGTGTATACATACAAGGGAACATTACTCTGCAATAAAAAGGAAC ATCAACTGACAGATAAAATGTGGTGTATACATGCAAGGGAACATTACTCTGCAATAAAAAGGAAC T C IP6K1 Ensembl:ENSG00000176095 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1000658357 Functional Loss SNV dbSNP153 33..33 33 - - - 29569 RMVar_ID_29569 Human_SNP_ID_132610635 A-to-I Human chr3 - 49779432 49779432 49779432 AAATGAAAACAAATGTTCACACAAAAACTTGTACATGAATGTTTATGGCAGCATTATTCATAATA AAATGAAAACAAATGTTCACACAAAAACTTGTGCATGAATGTTTATGGCAGCATTATTCATAATA T C IP6K1 Ensembl:ENSG00000176095 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1478654184 Functional Loss SNV dbSNP153 33..33 33 - - - 29570 RMVar_ID_29570 Human_SNP_ID_132611101 A-to-I Human chr3 - 49781164 49781164 49781164 CCAGCTACTTGGAAGATTGAAGCAGTAGAATCACTTGAACCTGGAAGGCAGAGGTTGCAGTGAGC CCAGCTACTTGGAAGATTGAAGCAGTAGAATCTCTTGAACCTGGAAGGCAGAGGTTGCAGTGAGC T A IP6K1 Ensembl:ENSG00000176095 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs568459440 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14871462 29571 RMVar_ID_29571 Human_SNP_ID_132611102 A-to-I Human chr3 - 49781164 49781164 49781164 CCAGCTACTTGGAAGATTGAAGCAGTAGAATCACTTGAACCTGGAAGGCAGAGGTTGCAGTGAGC CCAGCTACTTGGAAGATTGAAGCAGTAGAATCGCTTGAACCTGGAAGGCAGAGGTTGCAGTGAGC T C IP6K1 Ensembl:ENSG00000176095 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs568459440 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14871462 29572 RMVar_ID_29572 Human_SNP_ID_132611105 A-to-I Human chr3 - 49781173 49781173 49781173 CTTGTAATCCCAGCTACTTGGAAGATTGAAGCAGTAGAATCACTTGAACCTGGAAGGCAGAGGTT CTTGTAATCCCAGCTACTTGGAAGATTGAAGCGGTAGAATCACTTGAACCTGGAAGGCAGAGGTT T C IP6K1 Ensembl:ENSG00000176095 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs895087103 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14871462 29573 RMVar_ID_29573 Human_SNP_ID_132616187 A-to-I Human chr3 - 49798453 49798453 49798453 CTCCCGAGTAGCTGGGACTACAGGCACCCGCCACCACGCCCGGCTAATTTTTTTGTATTTTGTAG CTCCCGAGTAGCTGGGACTACAGGCACCCGCCGCCACGCCCGGCTAATTTTTTTGTATTTTGTAG T C CDHR4 Ensembl:ENSG00000187492 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1259862621 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115134,RMVar_hsa_circ_218280 29574 RMVar_ID_29574 Human_SNP_ID_132616191 A-to-I Human chr3 - 49798460 49798460 49798460 CCTCAGCCTCCCGAGTAGCTGGGACTACAGGCACCCGCCACCACGCCCGGCTAATTTTTTTGTAT CCTCAGCCTCCCGAGTAGCTGGGACTACAGGCTCCCGCCACCACGCCCGGCTAATTTTTTTGTAT T A CDHR4 Ensembl:ENSG00000187492 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1399484584 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115134,RMVar_hsa_circ_218280 29575 RMVar_ID_29575 Human_SNP_ID_132616192 A-to-I Human chr3 - 49798460 49798460 49798460 CCTCAGCCTCCCGAGTAGCTGGGACTACAGGCACCCGCCACCACGCCCGGCTAATTTTTTTGTAT CCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCCGCCACCACGCCCGGCTAATTTTTTTGTAT T C CDHR4 Ensembl:ENSG00000187492 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1399484584 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115134,RMVar_hsa_circ_218280 29576 RMVar_ID_29576 Human_SNP_ID_132626213 A-to-I Human chr3 - 49837031 49837031 49837031 ATCACTTGAGCCTGGGAGGTCAAGACTGCAGTAAGTGATGATCACGCCACTGCACTCTAGTCTGG ATCACTTGAGCCTGGGAGGTCAAGACTGCAGTGAGTGATGATCACGCCACTGCACTCTAGTCTGG T C TRAIP Ensembl:ENSG00000183763 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1332381401 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25742718 RMVar_hsa_circ_15530,RMVar_hsa_circ_84340,RMVar_hsa_circ_218291 29577 RMVar_ID_29577 Human_SNP_ID_132648256 A-to-I Human chr3 + 49924580 49924580 49924580 GGGCGCCTGTAATCCCAACTGCTTGGGAGGCTAAGGTATGAGAATCACTTGAACCCGGGGGGAGG GGGCGCCTGTAATCCCAACTGCTTGGGAGGCTGAGGTATGAGAATCACTTGAACCCGGGGGGAGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1298022740 Functional Loss SNV dbSNP153 33..33 33 - - - 29578 RMVar_ID_29578 Human_SNP_ID_132650811 A-to-I Human chr3 - 49936054 49936054 49936054 GTTGCAGTACAGTGGCACGATCATAGCTCACTACAGCCTCGAACTCCTGGGTTCAAACAATGTGG GTTGCAGTACAGTGGCACGATCATAGCTCACTGCAGCCTCGAACTCCTGGGTTCAAACAATGTGG T C HSALNG0025985 RNACentral:URS0000E965BE lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1297171380 Functional Loss SNV dbSNP153 33..33 33 - - - 29579 RMVar_ID_29579 Human_SNP_ID_132653691 A-to-I Human chr3 + 49946665 49946665 49946665 TGAAGCAATTCTTGTGCCTCAGCCTCCCGGGTAGCTGGGATTACAGGCGTGTGCCACCACGCCTG TGAAGCAATTCTTGTGCCTCAGCCTCCCGGGTTGCTGGGATTACAGGCGTGTGCCACCACGCCTG A T RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965319744 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_218304,RMVar_hsa_circ_122766 29580 RMVar_ID_29580 Human_SNP_ID_132654357 A-to-I Human chr3 + 49949033 49949033 49949033 TTGTATTTTTAGTAGAGATGGAGTTTCACTATATTGGCCAGGCTGGTCTCAAATTTCTGACCTTG TTGTATTTTTAGTAGAGATGGAGTTTCACTATTTTGGCCAGGCTGGTCTCAAATTTCTGACCTTG A T RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1238529801 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_218304,RMVar_hsa_circ_122766 29581 RMVar_ID_29581 Human_SNP_ID_132654371 A-to-I Human chr3 + 49949081 49949081 49949081 TCAAATTTCTGACCTTGTGATCCGCTGGCCTCAGCCTCCCAAAGTGCTGGGACTACAGGTGTGAG TCAAATTTCTGACCTTGTGATCCGCTGGCCTCGGCCTCCCAAAGTGCTGGGACTACAGGTGTGAG A G RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1243747273 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_218304,RMVar_hsa_circ_122766 29582 RMVar_ID_29582 Human_SNP_ID_132655528 A-to-I Human chr3 + 49953703 49953703 49953703 TACCACGCCTGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCTACCTGG TACCACGCCTGGCTAATTTTTGTATTTTTAGTGGAGACGGGGTTTCACCATGTTGGCCTACCTGG A G RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1359618494 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_218304,RMVar_hsa_circ_122766 29583 RMVar_ID_29583 Human_SNP_ID_132655557 A-to-I Human chr3 + 49953796 49953795 49953796 CCCGCATCAGCCTCCCAAAGTGCTGGGGTTACAAGCGTGAGCCACCACGCCTAGCTGGACCTGAC CCCGCATCAGCCTCCCAAAGTGCTGGGGTTAC_AGCGTGAGCCACCACGCCTAGCTGGACCTGAC CA C RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs750390462 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_218304,RMVar_hsa_circ_122766 29584 RMVar_ID_29584 Human_SNP_ID_132655617 A-to-I Human chr3 + 49953989 49953989 49953989 CCCTAGGTCTACCAGAAATACACAAAAAAATTAGCCGAGCATGGTAGTGCACATTTGTAGTCCCA CCCTAGGTCTACCAGAAATACACAAAAAAATTGGCCGAGCATGGTAGTGCACATTTGTAGTCCCA A G RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1318179181 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_218304,RMVar_hsa_circ_122766 29585 RMVar_ID_29585 Human_SNP_ID_132655624 A-to-I Human chr3 + 49954002 49954000 49954002 AGAAATACACAAAAAAATTAGCCGAGCATGGTAGTGCACATTTGTAGTCCCAGCTACTCAGGAGG AGAAATACACAAAAAAATTAGCCGAGCATGG__GTGCACATTTGTAGTCCCAGCTACTCAGGAGG GTA G RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1448687516 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_218304,RMVar_hsa_circ_122766 29586 RMVar_ID_29586 Human_SNP_ID_132657080 A-to-I Human chr3 + 49958818 49958814 49958818 TTTTTTTTTTTTTTTTGTAAAAATGGAGTCTCACTCTGTTGCCCTGGCTGGAGTGCTGAGTGCCA TTTTTTTTTTTTTTTTGTAAAAATGGAGT____CTCTGTTGCCCTGGCTGGAGTGCTGAGTGCCA TCTCA T RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1272953119 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_17574092 RMVar_hsa_circ_218304,RMVar_hsa_circ_122766 29587 RMVar_ID_29587 Human_SNP_ID_132657082 A-to-I Human chr3 + 49958818 49958818 49958818 TTTTTTTTTTTTTTTTGTAAAAATGGAGTCTCACTCTGTTGCCCTGGCTGGAGTGCTGAGTGCCA TTTTTTTTTTTTTTTTGTAAAAATGGAGTCTCGCTCTGTTGCCCTGGCTGGAGTGCTGAGTGCCA A G RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs988448297 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17574092 RMVar_hsa_circ_218304,RMVar_hsa_circ_122766 29588 RMVar_ID_29588 Human_SNP_ID_132657131 A-to-I Human chr3 + 49959054 49959054 49959054 TGACCTCGTGACCAACCCACTTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGTGC TGACCTCGTGACCAACCCACTTCGGCCTCCCACAGTGCTGGGATTACAGGCGTGAGCCACTGTGC A C RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs983349572 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_218304,RMVar_hsa_circ_122766 29589 RMVar_ID_29589 Human_SNP_ID_132658247 A-to-I Human chr3 + 49962979 49962963 49962979 AAAACTAGCCGGGCGTGGTGGCGGCTGCCTGTAGTCCCAGCTACTCGGGAGGCTGAAGCAGGAGA AAAACTAGCCGGGCGTG________________GTCCCAGCTACTCGGGAGGCTGAAGCAGGAGA GGTGGCGGCTGCCTGTA G RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs766903689 Functional Loss DEL dbSNP153 18..33 33 - - - RMVar_hsa_circ_218306,RMVar_hsa_circ_349894,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_361486,RMVar_hsa_circ_125334,RMVar_hsa_circ_275697,RMVar_hsa_circ_54905,RMVar_hsa_circ_218305 29590 RMVar_ID_29590 Human_SNP_ID_132658506 A-to-I Human chr3 + 49964107 49964107 49964107 ATTTTTTTTTTTAGTAGAGATGGCGTTTCACCATGTTGGCCAGGCTGATCTCAAACTCCTGACCT ATTTTTTTTTTTAGTAGAGATGGCGTTTCACCGTGTTGGCCAGGCTGATCTCAAACTCCTGACCT A G RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1477942091 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_218306,RMVar_hsa_circ_349894,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_361486,RMVar_hsa_circ_125334,RMVar_hsa_circ_275697,RMVar_hsa_circ_54905,RMVar_hsa_circ_218305 29591 RMVar_ID_29591 Human_SNP_ID_132660142 A-to-I Human chr3 + 49970106 49970106 49970106 GGGACTGTAGTTGTGCACCACCAAATCTGACTAATTTTTGTATTTTTTGTAGAGATGAAGTTTAG GGGACTGTAGTTGTGCACCACCAAATCTGACTGATTTTTGTATTTTTTGTAGAGATGAAGTTTAG A G RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1299686056 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_349894,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_275697,RMVar_hsa_circ_54905,RMVar_hsa_circ_280801,RMVar_hsa_circ_288674,RMVar_hsa_circ_368344,RMVar_hsa_circ_218305,RMVar_hsa_circ_340484,RMVar_hsa_circ_306069,RMVar_hsa_circ_350418,RMVar_hsa_circ_272909,RMVar_hsa_circ_218309,RMVar_hsa_circ_41547,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_218307,RMVar_hsa_circ_218308 29592 RMVar_ID_29592 Human_SNP_ID_132660330 A-to-I Human chr3 + 49971145 49971145 49971145 AAAATTAGCTGGGCGTAGTGATGCATGTGTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTAGCTGGGCGTAGTGATGCATGTGTGTCATCCCAGCTACTCGGGAGGCTGAGGCAGGAGA A C RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1258924428 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_349894,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_275697,RMVar_hsa_circ_54905,RMVar_hsa_circ_280801,RMVar_hsa_circ_288674,RMVar_hsa_circ_368344,RMVar_hsa_circ_218305,RMVar_hsa_circ_340484,RMVar_hsa_circ_306069,RMVar_hsa_circ_350418,RMVar_hsa_circ_272909,RMVar_hsa_circ_218309,RMVar_hsa_circ_41547,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_218307,RMVar_hsa_circ_218308 29593 RMVar_ID_29593 Human_SNP_ID_132660385 A-to-I Human chr3 + 49971324 49971324 49971324 AAAACCAGCCAGGTGTGGAGGTGGGCGCCTGTAATCCCAACTACTTGGGAGGCTGAGGCAGGAGA AAAACCAGCCAGGTGTGGAGGTGGGCGCCTGTTATCCCAACTACTTGGGAGGCTGAGGCAGGAGA A T RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1219425196 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_349894,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_275697,RMVar_hsa_circ_54905,RMVar_hsa_circ_280801,RMVar_hsa_circ_288674,RMVar_hsa_circ_368344,RMVar_hsa_circ_218305,RMVar_hsa_circ_340484,RMVar_hsa_circ_306069,RMVar_hsa_circ_350418,RMVar_hsa_circ_272909,RMVar_hsa_circ_218309,RMVar_hsa_circ_41547,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_218307,RMVar_hsa_circ_218308 29594 RMVar_ID_29594 Human_SNP_ID_132661992 A-to-I Human chr3 + 49978015 49978015 49978015 TAGTAGTAACAGTGACTTAAAAATTTTTTTTTATAAGAGAAAGGGTCTTACTCTGTTGCCCAGGT TAGTAGTAACAGTGACTTAAAAATTTTTTTTTGTAAGAGAAAGGGTCTTACTCTGTTGCCCAGGT A G RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1217866921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7205788,Human_RBP_ID_17573423 RMVar_hsa_circ_15596,RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_54905,RMVar_hsa_circ_280801,RMVar_hsa_circ_368344,RMVar_hsa_circ_306069,RMVar_hsa_circ_350418,RMVar_hsa_circ_218309,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_290547,RMVar_hsa_circ_306473,RMVar_hsa_circ_68132,RMVar_hsa_circ_218313,RMVar_hsa_circ_218311,RMVar_hsa_circ_218312,RMVar_hsa_circ_334070 29595 RMVar_ID_29595 Human_SNP_ID_132661993 A-to-I Human chr3 + 49978017 49978017 49978017 GTAGTAACAGTGACTTAAAAATTTTTTTTTATAAGAGAAAGGGTCTTACTCTGTTGCCCAGGTTG GTAGTAACAGTGACTTAAAAATTTTTTTTTATGAGAGAAAGGGTCTTACTCTGTTGCCCAGGTTG A G RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1482584195 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7205788,Human_RBP_ID_17573423 RMVar_hsa_circ_15596,RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_54905,RMVar_hsa_circ_280801,RMVar_hsa_circ_368344,RMVar_hsa_circ_306069,RMVar_hsa_circ_350418,RMVar_hsa_circ_218309,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_290547,RMVar_hsa_circ_306473,RMVar_hsa_circ_68132,RMVar_hsa_circ_218313,RMVar_hsa_circ_218311,RMVar_hsa_circ_218312,RMVar_hsa_circ_334070 29596 RMVar_ID_29596 Human_SNP_ID_132662013 A-to-I Human chr3 + 49978100 49978100 49978100 ATAGCTTACTGTAACCTCAAACCCCTCGGCTCAAGTGATCCTTCTGTCTCAACCTCCAGAGTATT ATAGCTTACTGTAACCTCAAACCCCTCGGCTCCAGTGATCCTTCTGTCTCAACCTCCAGAGTATT A C RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1194834769 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15596,RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_54905,RMVar_hsa_circ_280801,RMVar_hsa_circ_368344,RMVar_hsa_circ_306069,RMVar_hsa_circ_350418,RMVar_hsa_circ_218309,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_290547,RMVar_hsa_circ_306473,RMVar_hsa_circ_68132,RMVar_hsa_circ_218313,RMVar_hsa_circ_218311,RMVar_hsa_circ_218312,RMVar_hsa_circ_334070 29597 RMVar_ID_29597 Human_SNP_ID_132662406 A-to-I Human chr3 + 49979709 49979709 49979709 GTTATCTACCTGCCTGGGCCTCCCAAAGAGCTAGCATTACAGGAGTGAGCCACTGTGCCCAGCCA GTTATCTACCTGCCTGGGCCTCCCAAAGAGCTGGCATTACAGGAGTGAGCCACTGTGCCCAGCCA A G RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1431621278 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15596,RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_54905,RMVar_hsa_circ_280801,RMVar_hsa_circ_368344,RMVar_hsa_circ_306069,RMVar_hsa_circ_350418,RMVar_hsa_circ_218309,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_290547,RMVar_hsa_circ_306473,RMVar_hsa_circ_68132,RMVar_hsa_circ_218313,RMVar_hsa_circ_218311,RMVar_hsa_circ_218312,RMVar_hsa_circ_334070 29598 RMVar_ID_29598 Human_SNP_ID_132662407 A-to-I Human chr3 + 49979709 49979709 49979709 GTTATCTACCTGCCTGGGCCTCCCAAAGAGCTAGCATTACAGGAGTGAGCCACTGTGCCCAGCCA GTTATCTACCTGCCTGGGCCTCCCAAAGAGCTTGCATTACAGGAGTGAGCCACTGTGCCCAGCCA A T RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1431621278 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15596,RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_54905,RMVar_hsa_circ_280801,RMVar_hsa_circ_368344,RMVar_hsa_circ_306069,RMVar_hsa_circ_350418,RMVar_hsa_circ_218309,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_290547,RMVar_hsa_circ_306473,RMVar_hsa_circ_68132,RMVar_hsa_circ_218313,RMVar_hsa_circ_218311,RMVar_hsa_circ_218312,RMVar_hsa_circ_334070 29599 RMVar_ID_29599 Human_SNP_ID_132662513 A-to-I Human chr3 + 49980194 49980194 49980194 TAGCTAATTTTTGTATTTTTTTTAGTAGCGACAGGGTTGCGCCATGTTGACCAGGCTGGTCTTGA TAGCTAATTTTTGTATTTTTTTTAGTAGCGACGGGGTTGCGCCATGTTGACCAGGCTGGTCTTGA A G RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1216473313 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14979264 RMVar_hsa_circ_15596,RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_54905,RMVar_hsa_circ_280801,RMVar_hsa_circ_368344,RMVar_hsa_circ_306069,RMVar_hsa_circ_350418,RMVar_hsa_circ_218309,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_290547,RMVar_hsa_circ_306473,RMVar_hsa_circ_68132,RMVar_hsa_circ_218313,RMVar_hsa_circ_218311,RMVar_hsa_circ_218312,RMVar_hsa_circ_334070 29600 RMVar_ID_29600 Human_SNP_ID_132663480 A-to-I Human chr3 + 49984121 49984121 49984121 CGAGACCACCCTGGGCAACATGGTGAAACTCTATCTCTCCAAAAAAAATACAAAAAAAATTAGCT CGAGACCACCCTGGGCAACATGGTGAAACTCTCTCTCTCCAAAAAAAATACAAAAAAAATTAGCT A C RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs375637403 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15596,RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_54905,RMVar_hsa_circ_280801,RMVar_hsa_circ_368344,RMVar_hsa_circ_306069,RMVar_hsa_circ_350418,RMVar_hsa_circ_218309,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_290547,RMVar_hsa_circ_306473,RMVar_hsa_circ_68132,RMVar_hsa_circ_218313,RMVar_hsa_circ_218311,RMVar_hsa_circ_218312,RMVar_hsa_circ_334070 29601 RMVar_ID_29601 Human_SNP_ID_132663481 A-to-I Human chr3 + 49984121 49984121 49984121 CGAGACCACCCTGGGCAACATGGTGAAACTCTATCTCTCCAAAAAAAATACAAAAAAAATTAGCT CGAGACCACCCTGGGCAACATGGTGAAACTCTGTCTCTCCAAAAAAAATACAAAAAAAATTAGCT A G RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs375637403 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15596,RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_54905,RMVar_hsa_circ_280801,RMVar_hsa_circ_368344,RMVar_hsa_circ_306069,RMVar_hsa_circ_350418,RMVar_hsa_circ_218309,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_290547,RMVar_hsa_circ_306473,RMVar_hsa_circ_68132,RMVar_hsa_circ_218313,RMVar_hsa_circ_218311,RMVar_hsa_circ_218312,RMVar_hsa_circ_334070 29602 RMVar_ID_29602 Human_SNP_ID_132663545 A-to-I Human chr3 + 49984349 49984349 49984349 GTGAATGTAAAATAAAATGGTAGCTCACGCCTATAATCCTGGTACTTTGGGAGGCCGAGATGGGT GTGAATGTAAAATAAAATGGTAGCTCACGCCTGTAATCCTGGTACTTTGGGAGGCCGAGATGGGT A G RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1559552428 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15596,RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_54905,RMVar_hsa_circ_280801,RMVar_hsa_circ_368344,RMVar_hsa_circ_306069,RMVar_hsa_circ_350418,RMVar_hsa_circ_218309,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_290547,RMVar_hsa_circ_306473,RMVar_hsa_circ_68132,RMVar_hsa_circ_218313,RMVar_hsa_circ_218311,RMVar_hsa_circ_218312,RMVar_hsa_circ_334070 29603 RMVar_ID_29603 Human_SNP_ID_132663564 A-to-I Human chr3 + 49984437 49984437 49984437 CAGACCAGCCTGGTCAATATGGCAAAACTCCCATCTCTACTAAAAATACAAAAACTAGCTGGGCT CAGACCAGCCTGGTCAATATGGCAAAACTCCCTTCTCTACTAAAAATACAAAAACTAGCTGGGCT A T RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1010066863 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15596,RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_54905,RMVar_hsa_circ_280801,RMVar_hsa_circ_368344,RMVar_hsa_circ_306069,RMVar_hsa_circ_350418,RMVar_hsa_circ_218309,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_290547,RMVar_hsa_circ_306473,RMVar_hsa_circ_68132,RMVar_hsa_circ_218313,RMVar_hsa_circ_218311,RMVar_hsa_circ_218312,RMVar_hsa_circ_334070 29604 RMVar_ID_29604 Human_SNP_ID_132664649 A-to-I Human chr3 + 49988372 49988372 49988372 CACTGTCTTGCCCAGGCAGGTCTTGAACTCCTAAGCTCAAACAACCGTCCTGCCTTGCCCTCCCA CACTGTCTTGCCCAGGCAGGTCTTGAACTCCTGAGCTCAAACAACCGTCCTGCCTTGCCCTCCCA A G RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1288410882 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15596,RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_54905,RMVar_hsa_circ_280801,RMVar_hsa_circ_368344,RMVar_hsa_circ_306069,RMVar_hsa_circ_350418,RMVar_hsa_circ_218309,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_290547,RMVar_hsa_circ_306473,RMVar_hsa_circ_68132,RMVar_hsa_circ_218313,RMVar_hsa_circ_218311,RMVar_hsa_circ_218312,RMVar_hsa_circ_334070 29605 RMVar_ID_29605 Human_SNP_ID_132664866 A-to-I Human chr3 + 49989297 49989297 49989297 TATGCCAATCGGTTAAATAATATTTGTGGGCCAGGCCCGGTGGCTCATGCCTGTAATGCCAGCAC TATGCCAATCGGTTAAATAATATTTGTGGGCCGGGCCCGGTGGCTCATGCCTGTAATGCCAGCAC A G RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1168115955 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15596,RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_54905,RMVar_hsa_circ_280801,RMVar_hsa_circ_368344,RMVar_hsa_circ_306069,RMVar_hsa_circ_350418,RMVar_hsa_circ_218309,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_290547,RMVar_hsa_circ_306473,RMVar_hsa_circ_68132,RMVar_hsa_circ_218313,RMVar_hsa_circ_218311,RMVar_hsa_circ_218312,RMVar_hsa_circ_334070 29606 RMVar_ID_29606 Human_SNP_ID_132665007 A-to-I Human chr3 + 49989864 49989864 49989864 CGCCTCCCAGATTCAAGCCATTCTCGTGCCTCAGCCTCCCTTGTAGCTGGGATTACAGTTGCCCA CGCCTCCCAGATTCAAGCCATTCTCGTGCCTCGGCCTCCCTTGTAGCTGGGATTACAGTTGCCCA A G RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984725997 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15596,RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_54905,RMVar_hsa_circ_280801,RMVar_hsa_circ_368344,RMVar_hsa_circ_306069,RMVar_hsa_circ_350418,RMVar_hsa_circ_218309,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_290547,RMVar_hsa_circ_306473,RMVar_hsa_circ_68132,RMVar_hsa_circ_218313,RMVar_hsa_circ_218311,RMVar_hsa_circ_218312,RMVar_hsa_circ_334070 29607 RMVar_ID_29607 Human_SNP_ID_132665019 A-to-I Human chr3 + 49989927 49989927 49989927 CACCACCACGCCTGGCTGATTTTTGTATTTTTAGTAGAGATGAGGTTTCACCATGTTGGCCACGC CACCACCACGCCTGGCTGATTTTTGTATTTTTGGTAGAGATGAGGTTTCACCATGTTGGCCACGC A G RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs896029086 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15596,RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_54905,RMVar_hsa_circ_280801,RMVar_hsa_circ_368344,RMVar_hsa_circ_306069,RMVar_hsa_circ_350418,RMVar_hsa_circ_218309,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_290547,RMVar_hsa_circ_306473,RMVar_hsa_circ_68132,RMVar_hsa_circ_218313,RMVar_hsa_circ_218311,RMVar_hsa_circ_218312,RMVar_hsa_circ_334070 29608 RMVar_ID_29608 Human_SNP_ID_132665483 A-to-I Human chr3 + 49992091 49992091 49992091 CTTCCGTTTCAGCCTCCCAAGTAGCTGAGATTACAGGTGTGTACCACGACACCTGGCTGATTTAA CTTCCGTTTCAGCCTCCCAAGTAGCTGAGATTGCAGGTGTGTACCACGACACCTGGCTGATTTAA A G RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs951163983 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15596,RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_54905,RMVar_hsa_circ_280801,RMVar_hsa_circ_368344,RMVar_hsa_circ_306069,RMVar_hsa_circ_350418,RMVar_hsa_circ_218309,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_290547,RMVar_hsa_circ_306473,RMVar_hsa_circ_68132,RMVar_hsa_circ_218313,RMVar_hsa_circ_218311,RMVar_hsa_circ_218312,RMVar_hsa_circ_334070 29609 RMVar_ID_29609 Human_SNP_ID_132665484 A-to-I Human chr3 + 49992091 49992091 49992091 CTTCCGTTTCAGCCTCCCAAGTAGCTGAGATTACAGGTGTGTACCACGACACCTGGCTGATTTAA CTTCCGTTTCAGCCTCCCAAGTAGCTGAGATTTCAGGTGTGTACCACGACACCTGGCTGATTTAA A T RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs951163983 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15596,RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_54905,RMVar_hsa_circ_280801,RMVar_hsa_circ_368344,RMVar_hsa_circ_306069,RMVar_hsa_circ_350418,RMVar_hsa_circ_218309,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_290547,RMVar_hsa_circ_306473,RMVar_hsa_circ_68132,RMVar_hsa_circ_218313,RMVar_hsa_circ_218311,RMVar_hsa_circ_218312,RMVar_hsa_circ_334070 29610 RMVar_ID_29610 Human_SNP_ID_132665495 A-to-I Human chr3 + 49992140 49992139 49992140 CACCTGGCTGATTTAAAACCTTTTGTAGAGATAGTGTCCCAGTGTGTTTGCCCAGGCTGGTCTCA CACCTGGCTGATTTAAAACCTTTTGTAGAGAT_GTGTCCCAGTGTGTTTGCCCAGGCTGGTCTCA TA T RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1414273242 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_7205841,Human_RBP_ID_14873372 RMVar_hsa_circ_15596,RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_54905,RMVar_hsa_circ_280801,RMVar_hsa_circ_368344,RMVar_hsa_circ_306069,RMVar_hsa_circ_350418,RMVar_hsa_circ_218309,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_290547,RMVar_hsa_circ_306473,RMVar_hsa_circ_68132,RMVar_hsa_circ_218313,RMVar_hsa_circ_218311,RMVar_hsa_circ_218312,RMVar_hsa_circ_334070 29611 RMVar_ID_29611 Human_SNP_ID_132668460 A-to-I Human chr3 + 50005375 50005375 50005375 TAAAAATTAGCTGGGTGTAGTGGCACATGCCTATTGTCCCAGCTATTTGGAAGGCTAAAGTGGGA TAAAAATTAGCTGGGTGTAGTGGCACATGCCTGTTGTCCCAGCTATTTGGAAGGCTAAAGTGGGA A G RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs897201785 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15596,RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_280801,RMVar_hsa_circ_350418,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_306473,RMVar_hsa_circ_68132,RMVar_hsa_circ_218313,RMVar_hsa_circ_218311,RMVar_hsa_circ_334070 29612 RMVar_ID_29612 Human_SNP_ID_132668465 A-to-I Human chr3 + 50005399 50005399 50005399 ACATGCCTATTGTCCCAGCTATTTGGAAGGCTAAAGTGGGAGGATTGCTTGAGCCTGGGAGGTCA ACATGCCTATTGTCCCAGCTATTTGGAAGGCTGAAGTGGGAGGATTGCTTGAGCCTGGGAGGTCA A G RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1450026610 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17573670 RMVar_hsa_circ_15596,RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_280801,RMVar_hsa_circ_350418,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_306473,RMVar_hsa_circ_68132,RMVar_hsa_circ_218313,RMVar_hsa_circ_218311,RMVar_hsa_circ_334070 29613 RMVar_ID_29613 Human_SNP_ID_132669761 A-to-I Human chr3 + 50010641 50010641 50010641 AACTTTTTTTAAGGCCAGGCAGGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGC AACTTTTTTTAAGGCCAGGCAGGGTGGCTCACCCCTGTAATCCCAGCACTTTGGGAGGCTGAGGC A C RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs546615314 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15596,RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_280801,RMVar_hsa_circ_350418,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_306473,RMVar_hsa_circ_68132,RMVar_hsa_circ_218313,RMVar_hsa_circ_218311,RMVar_hsa_circ_334070 29614 RMVar_ID_29614 Human_SNP_ID_132669762 A-to-I Human chr3 + 50010641 50010641 50010641 AACTTTTTTTAAGGCCAGGCAGGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGC AACTTTTTTTAAGGCCAGGCAGGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGC A G RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs546615314 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15596,RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_280801,RMVar_hsa_circ_350418,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_306473,RMVar_hsa_circ_68132,RMVar_hsa_circ_218313,RMVar_hsa_circ_218311,RMVar_hsa_circ_334070 29615 RMVar_ID_29615 Human_SNP_ID_132669796 A-to-I Human chr3 + 50010782 50010782 50010782 AAAATTAGCCCAGCATGGTGGTGTGTTCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTAGCCCAGCATGGTGGTGTGTTCCTGTGGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA A G RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1020960152 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15596,RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_280801,RMVar_hsa_circ_350418,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_306473,RMVar_hsa_circ_68132,RMVar_hsa_circ_218313,RMVar_hsa_circ_218311,RMVar_hsa_circ_334070 29616 RMVar_ID_29616 Human_SNP_ID_132670377 A-to-I Human chr3 + 50012914 50012914 50012914 ACAGCCATGCGCCACCACGCCTGGCTAATTTTATATTTTTTAGTGGAGACCAGGTTCCTCCATGT ACAGCCATGCGCCACCACGCCTGGCTAATTTTGTATTTTTTAGTGGAGACCAGGTTCCTCCATGT A G RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946555516 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14874226 RMVar_hsa_circ_15596,RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_280801,RMVar_hsa_circ_350418,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_306473,RMVar_hsa_circ_68132,RMVar_hsa_circ_218313,RMVar_hsa_circ_218311,RMVar_hsa_circ_334070 29617 RMVar_ID_29617 Human_SNP_ID_132670378 A-to-I Human chr3 + 50012914 50012914 50012914 ACAGCCATGCGCCACCACGCCTGGCTAATTTTATATTTTTTAGTGGAGACCAGGTTCCTCCATGT ACAGCCATGCGCCACCACGCCTGGCTAATTTTTTATTTTTTAGTGGAGACCAGGTTCCTCCATGT A T RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946555516 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14874226 RMVar_hsa_circ_15596,RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_280801,RMVar_hsa_circ_350418,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_306473,RMVar_hsa_circ_68132,RMVar_hsa_circ_218313,RMVar_hsa_circ_218311,RMVar_hsa_circ_334070 29618 RMVar_ID_29618 Human_SNP_ID_132670513 A-to-I Human chr3 + 50013459 50013458 50013460 TTCAGAGGCCGAGGGAGGCGGATCACGAGGTCAAGAGATCAAGACCATCCTGGCCTCGTGGTGAA TTCAGAGGCCGAGGGAGGCGGATCACGAGGTC__GAGATCAAGACCATCCTGGCCTCGTGGTGAA CAA C RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs746823920 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_15596,RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_280801,RMVar_hsa_circ_350418,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_306473,RMVar_hsa_circ_68132,RMVar_hsa_circ_218313,RMVar_hsa_circ_218311,RMVar_hsa_circ_334070 29619 RMVar_ID_29619 Human_SNP_ID_132670514 A-to-I Human chr3 + 50013459 50013459 50013459 TTCAGAGGCCGAGGGAGGCGGATCACGAGGTCAAGAGATCAAGACCATCCTGGCCTCGTGGTGAA TTCAGAGGCCGAGGGAGGCGGATCACGAGGTCTAGAGATCAAGACCATCCTGGCCTCGTGGTGAA A T RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1208615892 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15596,RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_280801,RMVar_hsa_circ_350418,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_306473,RMVar_hsa_circ_68132,RMVar_hsa_circ_218313,RMVar_hsa_circ_218311,RMVar_hsa_circ_334070 29620 RMVar_ID_29620 Human_SNP_ID_132672649 A-to-I Human chr3 + 50021814 50021814 50021814 TCACTTTGTTGCCCAGGCTGGAGTGTGGCGGCACGATCTTGGCTCACTGCAACCTCTCTACCTCC TCACTTTGTTGCCCAGGCTGGAGTGTGGCGGCGCGATCTTGGCTCACTGCAACCTCTCTACCTCC A G RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1452875376 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15596,RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_280801,RMVar_hsa_circ_350418,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_306473,RMVar_hsa_circ_68132,RMVar_hsa_circ_218313,RMVar_hsa_circ_218311,RMVar_hsa_circ_334070 29621 RMVar_ID_29621 Human_SNP_ID_132673135 A-to-I Human chr3 + 50023766 50023766 50023766 CAACCTCCGAGTTCAAGTGATTCTCGTGCCTCAGCCTCTCGAGTAGCTGGGATTACAGGCACCCG CAACCTCCGAGTTCAAGTGATTCTCGTGCCTCTGCCTCTCGAGTAGCTGGGATTACAGGCACCCG A T RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs541837059 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15596,RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_280801,RMVar_hsa_circ_350418,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_306473,RMVar_hsa_circ_68132,RMVar_hsa_circ_218313,RMVar_hsa_circ_218311,RMVar_hsa_circ_334070 29622 RMVar_ID_29622 Human_SNP_ID_132673678 A-to-I Human chr3 + 50025923 50025923 50025923 GTATAGAACTTTGACCAACATGGTGAAACCCCATCTCTACTAGAAATACAAAAATTAGCTGGGTG GTATAGAACTTTGACCAACATGGTGAAACCCCGTCTCTACTAGAAATACAAAAATTAGCTGGGTG A G RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1435908517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14874645 RMVar_hsa_circ_15596,RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_280801,RMVar_hsa_circ_350418,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_306473,RMVar_hsa_circ_68132,RMVar_hsa_circ_218313,RMVar_hsa_circ_218311,RMVar_hsa_circ_334070 29623 RMVar_ID_29623 Human_SNP_ID_132673681 A-to-I Human chr3 + 50025932 50025932 50025932 TTTGACCAACATGGTGAAACCCCATCTCTACTAGAAATACAAAAATTAGCTGGGTGTGGTGGCAG TTTGACCAACATGGTGAAACCCCATCTCTACTGGAAATACAAAAATTAGCTGGGTGTGGTGGCAG A G RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1034800510 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15596,RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_280801,RMVar_hsa_circ_350418,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_306473,RMVar_hsa_circ_68132,RMVar_hsa_circ_218313,RMVar_hsa_circ_218311,RMVar_hsa_circ_334070 29624 RMVar_ID_29624 Human_SNP_ID_132673707 A-to-I Human chr3 + 50026047 50026040 50026048 TGGAGGTTGCAGTGAACCAATATCAGACCACTATACTCCAGCTTGGATGACAGAGGGAGACTTTG TGGAGGTTGCAGTGAACCAATATCAG________ACTCCAGCTTGGATGACAGAGGGAGACTTTG GACCACTAT G RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1235096210 Functional Loss DEL dbSNP153 27..34 33 - - - RMVar_hsa_circ_15596,RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_280801,RMVar_hsa_circ_350418,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_306473,RMVar_hsa_circ_68132,RMVar_hsa_circ_218313,RMVar_hsa_circ_218311,RMVar_hsa_circ_334070 29625 RMVar_ID_29625 Human_SNP_ID_132673710 A-to-I Human chr3 + 50026047 50026047 50026047 TGGAGGTTGCAGTGAACCAATATCAGACCACTATACTCCAGCTTGGATGACAGAGGGAGACTTTG TGGAGGTTGCAGTGAACCAATATCAGACCACTGTACTCCAGCTTGGATGACAGAGGGAGACTTTG A G RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1057497714 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15596,RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_280801,RMVar_hsa_circ_350418,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_306473,RMVar_hsa_circ_68132,RMVar_hsa_circ_218313,RMVar_hsa_circ_218311,RMVar_hsa_circ_334070 29626 RMVar_ID_29626 Human_SNP_ID_132675212 A-to-I Human chr3 + 50032368 50032368 50032368 TAGCTGGGCGTGGTGGTGCGTGCCTGTAGTCCAAGCTACTCAGGAGGCTGAGGCAGGAGAATTGG TAGCTGGGCGTGGTGGTGCGTGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATTGG A C RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1559609529 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15596,RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_280801,RMVar_hsa_circ_350418,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_306473,RMVar_hsa_circ_68132,RMVar_hsa_circ_218313,RMVar_hsa_circ_218311,RMVar_hsa_circ_334070 29627 RMVar_ID_29627 Human_SNP_ID_132675446 A-to-I Human chr3 + 50033190 50033190 50033190 ATGGTGGTGCATACCGGTAATCCCAGCTACTCAGGAGGCTCAGACAGGAGAAGTGCTTGAACCCG ATGGTGGTGCATACCGGTAATCCCAGCTACTCCGGAGGCTCAGACAGGAGAAGTGCTTGAACCCG A C RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1376339534 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14874832 RMVar_hsa_circ_15596,RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_280801,RMVar_hsa_circ_350418,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_306473,RMVar_hsa_circ_68132,RMVar_hsa_circ_218313,RMVar_hsa_circ_218311,RMVar_hsa_circ_334070 29628 RMVar_ID_29628 Human_SNP_ID_132675573 A-to-I Human chr3 + 50033708 50033708 50033708 TCGCTCTGTCACCAGGTGGAGTGCAGTGGCGTAATCTCAGCTCACTGCAAGCTCTGCCTCCCAGG TCGCTCTGTCACCAGGTGGAGTGCAGTGGCGTGATCTCAGCTCACTGCAAGCTCTGCCTCCCAGG A G RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs980702596 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15596,RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_280801,RMVar_hsa_circ_350418,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_306473,RMVar_hsa_circ_68132,RMVar_hsa_circ_218313,RMVar_hsa_circ_218311,RMVar_hsa_circ_334070 29629 RMVar_ID_29629 Human_SNP_ID_132675819 A-to-I Human chr3 + 50034653 50034653 50034653 TGTAGTAGCGCATGCTTGTAATCCCAGCTACTAGGGAGGCTGAGTCAGGAGAATTGCTTGAACCC TGTAGTAGCGCATGCTTGTAATCCCAGCTACTTGGGAGGCTGAGTCAGGAGAATTGCTTGAACCC A T RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1301607794 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15596,RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_280801,RMVar_hsa_circ_350418,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_306473,RMVar_hsa_circ_68132,RMVar_hsa_circ_218313,RMVar_hsa_circ_218311,RMVar_hsa_circ_334070 29630 RMVar_ID_29630 Human_SNP_ID_132676034 A-to-I Human chr3 + 50035421 50035421 50035421 TAGAAACTTCAGGACAGGGTGCGGTGGCTCACACCTGTAATCTCAGCACTTTGGGAGGCCGAGGT TAGAAACTTCAGGACAGGGTGCGGTGGCTCACGCCTGTAATCTCAGCACTTTGGGAGGCCGAGGT A G RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs372352633 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15596,RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_280801,RMVar_hsa_circ_350418,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_306473,RMVar_hsa_circ_68132,RMVar_hsa_circ_218313,RMVar_hsa_circ_218311,RMVar_hsa_circ_334070 29631 RMVar_ID_29631 Human_SNP_ID_132676204 A-to-I Human chr3 + 50036020 50036020 50036020 CACACCTTGTGATCCACCCACCTTGGCCTCCCAAAGTGCTGGGATTACAGACGTGAGCCACTGCG CACACCTTGTGATCCACCCACCTTGGCCTCCCGAAGTGCTGGGATTACAGACGTGAGCCACTGCG A G RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs549449786 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15596,RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_280801,RMVar_hsa_circ_350418,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_306473,RMVar_hsa_circ_68132,RMVar_hsa_circ_218313,RMVar_hsa_circ_218311,RMVar_hsa_circ_334070 29632 RMVar_ID_29632 Human_SNP_ID_132676219 A-to-I Human chr3 + 50036098 50036098 50036098 TTATATTTTTGGTACAGACCAGGTTTCACTATATTGGCCAGGCTGTTCTCAAACTCCTGACCTCA TTATATTTTTGGTACAGACCAGGTTTCACTATGTTGGCCAGGCTGTTCTCAAACTCCTGACCTCA A G RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs146428585 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15596,RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_280801,RMVar_hsa_circ_350418,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_306473,RMVar_hsa_circ_68132,RMVar_hsa_circ_218313,RMVar_hsa_circ_218311,RMVar_hsa_circ_334070 29633 RMVar_ID_29633 Human_SNP_ID_132676441 A-to-I Human chr3 + 50036986 50036986 50036986 TTTTTAATTTTTAGTAGAGACGGGGCTTCACCATGTTGGCCAGTATGGTCTCGATCTCTTGACCT TTTTTAATTTTTAGTAGAGACGGGGCTTCACCGTGTTGGCCAGTATGGTCTCGATCTCTTGACCT A G RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs970910141 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15596,RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_280801,RMVar_hsa_circ_350418,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_306473,RMVar_hsa_circ_68132,RMVar_hsa_circ_218313,RMVar_hsa_circ_218311,RMVar_hsa_circ_334070 29634 RMVar_ID_29634 Human_SNP_ID_132676995 A-to-I Human chr3 + 50039369 50039369 50039369 TCAAGCGATGCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTAGAAGCGCCCATTACCACACCCA TCAAGCGATGCTCCTGCCTCAGCCTCCCGAGTGGCTGGGATTAGAAGCGCCCATTACCACACCCA A G RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1021382682 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15596,RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_280801,RMVar_hsa_circ_350418,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_306473,RMVar_hsa_circ_68132,RMVar_hsa_circ_218313,RMVar_hsa_circ_218311,RMVar_hsa_circ_334070 29635 RMVar_ID_29635 Human_SNP_ID_132677555 A-to-I Human chr3 + 50040786 50040786 50040786 TCAAGCAACCCTCCCACCTCAGCCCCTGGAGTAGTTAGGATAACAGGCGCACACTACCATTTTGT TCAAGCAACCCTCCCACCTCAGCCCCTGGAGTGGTTAGGATAACAGGCGCACACTACCATTTTGT A G RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1236337647 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15596,RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_280801,RMVar_hsa_circ_350418,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_306473,RMVar_hsa_circ_68132,RMVar_hsa_circ_218313,RMVar_hsa_circ_218311,RMVar_hsa_circ_334070 29636 RMVar_ID_29636 Human_SNP_ID_132680749 A-to-I Human chr3 + 50054917 50054917 50054917 GCAATCTCGGATCACTGCAAGCTCCGCCTCCCAGGTTCACGCTGTTCTCCTGCCTCAGCCTCTCT GCAATCTCGGATCACTGCAAGCTCCGCCTCCCGGGTTCACGCTGTTCTCCTGCCTCAGCCTCTCT A G RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1042538701 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_306473,RMVar_hsa_circ_68132,RMVar_hsa_circ_34312,RMVar_hsa_circ_56048,RMVar_hsa_circ_218313,RMVar_hsa_circ_218311,RMVar_hsa_circ_334070,RMVar_hsa_circ_350315,RMVar_hsa_circ_350814,RMVar_hsa_circ_292374,RMVar_hsa_circ_19240,RMVar_hsa_circ_353890,RMVar_hsa_circ_356555,RMVar_hsa_circ_71502,RMVar_hsa_circ_289790,RMVar_hsa_circ_37410,RMVar_hsa_circ_2194,RMVar_hsa_circ_218314,RMVar_hsa_circ_218316,RMVar_hsa_circ_8361,RMVar_hsa_circ_218317,RMVar_hsa_circ_218315,RMVar_hsa_circ_286024,RMVar_hsa_circ_286781,RMVar_hsa_circ_316435,RMVar_hsa_circ_355122,RMVar_hsa_circ_286658,RMVar_hsa_circ_46927,RMVar_hsa_circ_218318,RMVar_hsa_circ_218320,RMVar_hsa_circ_218321,RMVar_hsa_circ_218319 29637 RMVar_ID_29637 Human_SNP_ID_132680761 A-to-I Human chr3 + 50054985 50054985 50054985 AGCTGGGACTATAGGCGCCCACCACCATGCCCAGCTAATTATTTGTATTTTAGTAGAGACGGAGT AGCTGGGACTATAGGCGCCCACCACCATGCCCCGCTAATTATTTGTATTTTAGTAGAGACGGAGT A C RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs531589965 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_306473,RMVar_hsa_circ_68132,RMVar_hsa_circ_34312,RMVar_hsa_circ_56048,RMVar_hsa_circ_218313,RMVar_hsa_circ_218311,RMVar_hsa_circ_334070,RMVar_hsa_circ_350315,RMVar_hsa_circ_350814,RMVar_hsa_circ_292374,RMVar_hsa_circ_19240,RMVar_hsa_circ_353890,RMVar_hsa_circ_356555,RMVar_hsa_circ_71502,RMVar_hsa_circ_289790,RMVar_hsa_circ_37410,RMVar_hsa_circ_2194,RMVar_hsa_circ_218314,RMVar_hsa_circ_218316,RMVar_hsa_circ_8361,RMVar_hsa_circ_218317,RMVar_hsa_circ_218315,RMVar_hsa_circ_286024,RMVar_hsa_circ_286781,RMVar_hsa_circ_316435,RMVar_hsa_circ_355122,RMVar_hsa_circ_286658,RMVar_hsa_circ_46927,RMVar_hsa_circ_218318,RMVar_hsa_circ_218320,RMVar_hsa_circ_218321,RMVar_hsa_circ_218319 29638 RMVar_ID_29638 Human_SNP_ID_132682458 A-to-I Human chr3 - 50061767 50061767 50061767 CACATTCAGACCACCCACTGTCCACTTTTTCAAGAGCAACACTGTTCTTACCTGTATTGCCACAA CACATTCAGACCACCCACTGTCCACTTTTTCAGGAGCAACACTGTTCTTACCTGTATTGCCACAA T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs555807640 Functional Loss SNV dbSNP153 33..33 33 - - - 29639 RMVar_ID_29639 Human_SNP_ID_132682937 A-to-I Human chr3 + 50063739 50063739 50063739 CTAGCCAATATGGTGAAACCCCCATCTCTACTAAAAAGACAAAAATTAGCTGGACGTGGTGGCGC CTAGCCAATATGGTGAAACCCCCATCTCTACTGAAAAGACAAAAATTAGCTGGACGTGGTGGCGC A G RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs905705431 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_125334,RMVar_hsa_circ_218310,RMVar_hsa_circ_353890,RMVar_hsa_circ_37410,RMVar_hsa_circ_2194,RMVar_hsa_circ_218317,RMVar_hsa_circ_286024,RMVar_hsa_circ_355122,RMVar_hsa_circ_218318,RMVar_hsa_circ_98055,RMVar_hsa_circ_118835,RMVar_hsa_circ_218323,RMVar_hsa_circ_87115,RMVar_hsa_circ_218324,RMVar_hsa_circ_363975,RMVar_hsa_circ_85032,RMVar_hsa_circ_218326,RMVar_hsa_circ_73407,RMVar_hsa_circ_218327,RMVar_hsa_circ_218328,RMVar_hsa_circ_89926,RMVar_hsa_circ_96978,RMVar_hsa_circ_218329,RMVar_hsa_circ_218330 29640 RMVar_ID_29640 Human_SNP_ID_132682957 A-to-I Human chr3 + 50063790 50063790 50063790 GGACGTGGTGGCGCAAGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCTCTTGAA GGACGTGGTGGCGCAAGCCTGTAGTCCCAGCTGCTCAGGAGGCTGAGGCAGGAGAATCTCTTGAA A G RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1192920347 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_125334,RMVar_hsa_circ_218310,RMVar_hsa_circ_353890,RMVar_hsa_circ_37410,RMVar_hsa_circ_2194,RMVar_hsa_circ_218317,RMVar_hsa_circ_286024,RMVar_hsa_circ_355122,RMVar_hsa_circ_218318,RMVar_hsa_circ_98055,RMVar_hsa_circ_118835,RMVar_hsa_circ_218323,RMVar_hsa_circ_87115,RMVar_hsa_circ_218324,RMVar_hsa_circ_363975,RMVar_hsa_circ_85032,RMVar_hsa_circ_218326,RMVar_hsa_circ_73407,RMVar_hsa_circ_218327,RMVar_hsa_circ_218328,RMVar_hsa_circ_89926,RMVar_hsa_circ_96978,RMVar_hsa_circ_218329,RMVar_hsa_circ_218330 29641 RMVar_ID_29641 Human_SNP_ID_132683155 A-to-I Human chr3 + 50064741 50064741 50064741 ACCATGTTGGCCAGGCTGGAGCACAGTGGCACAATCTTGGCTCACTGCAAGCTCCGCCTCTCGGG ACCATGTTGGCCAGGCTGGAGCACAGTGGCACTATCTTGGCTCACTGCAAGCTCCGCCTCTCGGG A T RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1212445749 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_125334,RMVar_hsa_circ_218310,RMVar_hsa_circ_353890,RMVar_hsa_circ_37410,RMVar_hsa_circ_2194,RMVar_hsa_circ_218317,RMVar_hsa_circ_286024,RMVar_hsa_circ_355122,RMVar_hsa_circ_218318,RMVar_hsa_circ_98055,RMVar_hsa_circ_118835,RMVar_hsa_circ_218323,RMVar_hsa_circ_87115,RMVar_hsa_circ_218324,RMVar_hsa_circ_363975,RMVar_hsa_circ_85032,RMVar_hsa_circ_218326,RMVar_hsa_circ_73407,RMVar_hsa_circ_218327,RMVar_hsa_circ_218328,RMVar_hsa_circ_89926,RMVar_hsa_circ_96978,RMVar_hsa_circ_218329,RMVar_hsa_circ_218330 29642 RMVar_ID_29642 Human_SNP_ID_132685433 A-to-I Human chr3 + 50074966 50074966 50074966 GGTCAGGAGTTTGAGAGCAGCCTGGCCAACACAGTGAAACTCTGTCTCTACTGAAAAAAAAAAAA GGTCAGGAGTTTGAGAGCAGCCTGGCCAACACTGTGAAACTCTGTCTCTACTGAAAAAAAAAAAA A T RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1340668525 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_218306,RMVar_hsa_circ_125334,RMVar_hsa_circ_37410,RMVar_hsa_circ_98055,RMVar_hsa_circ_118835,RMVar_hsa_circ_218323,RMVar_hsa_circ_87115,RMVar_hsa_circ_218324,RMVar_hsa_circ_85032,RMVar_hsa_circ_218326,RMVar_hsa_circ_218327,RMVar_hsa_circ_81335,RMVar_hsa_circ_218328,RMVar_hsa_circ_89926,RMVar_hsa_circ_218333,RMVar_hsa_circ_101635,RMVar_hsa_circ_329296,RMVar_hsa_circ_218336 29643 RMVar_ID_29643 Human_SNP_ID_132685454 A-to-I Human chr3 + 50075097 50075097 50075097 AGAATCGCCTGAACCCAGGAGGCAGAGGTTGCAGTAAGCTGAGTTCGAGCCATTGCACTCCAGCC AGAATCGCCTGAACCCAGGAGGCAGAGGTTGCGGTAAGCTGAGTTCGAGCCATTGCACTCCAGCC A G RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs996292909 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_218306,RMVar_hsa_circ_125334,RMVar_hsa_circ_37410,RMVar_hsa_circ_98055,RMVar_hsa_circ_118835,RMVar_hsa_circ_218323,RMVar_hsa_circ_87115,RMVar_hsa_circ_218324,RMVar_hsa_circ_85032,RMVar_hsa_circ_218326,RMVar_hsa_circ_218327,RMVar_hsa_circ_81335,RMVar_hsa_circ_218328,RMVar_hsa_circ_89926,RMVar_hsa_circ_218333,RMVar_hsa_circ_101635,RMVar_hsa_circ_329296,RMVar_hsa_circ_218336 29644 RMVar_ID_29644 Human_SNP_ID_132685455 A-to-I Human chr3 + 50075097 50075097 50075097 AGAATCGCCTGAACCCAGGAGGCAGAGGTTGCAGTAAGCTGAGTTCGAGCCATTGCACTCCAGCC AGAATCGCCTGAACCCAGGAGGCAGAGGTTGCTGTAAGCTGAGTTCGAGCCATTGCACTCCAGCC A T RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs996292909 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_218306,RMVar_hsa_circ_125334,RMVar_hsa_circ_37410,RMVar_hsa_circ_98055,RMVar_hsa_circ_118835,RMVar_hsa_circ_218323,RMVar_hsa_circ_87115,RMVar_hsa_circ_218324,RMVar_hsa_circ_85032,RMVar_hsa_circ_218326,RMVar_hsa_circ_218327,RMVar_hsa_circ_81335,RMVar_hsa_circ_218328,RMVar_hsa_circ_89926,RMVar_hsa_circ_218333,RMVar_hsa_circ_101635,RMVar_hsa_circ_329296,RMVar_hsa_circ_218336 29645 RMVar_ID_29645 Human_SNP_ID_132691359 A-to-I Human chr3 + 50096305 50096305 50096305 GAGCCCAGGAGTTCAAGTCCAACCTGGACAACATGGTAAGACGCATCTCTCCAAAAAAAAAAAAA GAGCCCAGGAGTTCAAGTCCAACCTGGACAACGTGGTAAGACGCATCTCTCCAAAAAAAAAAAAA A G RBM5,RBM6 Ensembl:ENSG00000003756,Ensembl:ENSG00000004534 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1320278075 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25743530 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_96641,RMVar_hsa_circ_218343,RMVar_hsa_circ_6084,RMVar_hsa_circ_218342,RMVar_hsa_circ_109449,RMVar_hsa_circ_93262,RMVar_hsa_circ_218348,RMVar_hsa_circ_54594,RMVar_hsa_circ_275888,RMVar_hsa_circ_218344,RMVar_hsa_circ_218345,RMVar_hsa_circ_218346,RMVar_hsa_circ_365390,RMVar_hsa_circ_285567,RMVar_hsa_circ_92660,RMVar_hsa_circ_114763,RMVar_hsa_circ_66297,RMVar_hsa_circ_218350,RMVar_hsa_circ_218351,RMVar_hsa_circ_218352,RMVar_hsa_circ_218349 29646 RMVar_ID_29646 Human_SNP_ID_132691463 A-to-I Human chr3 + 50096690 50096690 50096690 TGGCTCACAGCAGCCTCCAACTTTTGGGGCTCAGGCAATCCACCAGCCTCAGCCTCCCAAGTAGC TGGCTCACAGCAGCCTCCAACTTTTGGGGCTCCGGCAATCCACCAGCCTCAGCCTCCCAAGTAGC A C RBM5,RBM6 Ensembl:ENSG00000003756,Ensembl:ENSG00000004534 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1429252898 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17573683 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_96641,RMVar_hsa_circ_218343,RMVar_hsa_circ_6084,RMVar_hsa_circ_218342,RMVar_hsa_circ_109449,RMVar_hsa_circ_93262,RMVar_hsa_circ_218348,RMVar_hsa_circ_54594,RMVar_hsa_circ_275888,RMVar_hsa_circ_218344,RMVar_hsa_circ_218345,RMVar_hsa_circ_218346,RMVar_hsa_circ_365390,RMVar_hsa_circ_285567,RMVar_hsa_circ_92660,RMVar_hsa_circ_114763,RMVar_hsa_circ_66297,RMVar_hsa_circ_218350,RMVar_hsa_circ_218351,RMVar_hsa_circ_218352,RMVar_hsa_circ_218349 29647 RMVar_ID_29647 Human_SNP_ID_132691468 A-to-I Human chr3 + 50096702 50096702 50096702 GCCTCCAACTTTTGGGGCTCAGGCAATCCACCAGCCTCAGCCTCCCAAGTAGCTGGGATTACAGG GCCTCCAACTTTTGGGGCTCAGGCAATCCACCGGCCTCAGCCTCCCAAGTAGCTGGGATTACAGG A G RBM5,RBM6 Ensembl:ENSG00000003756,Ensembl:ENSG00000004534 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs991456355 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17573684 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_96641,RMVar_hsa_circ_218343,RMVar_hsa_circ_6084,RMVar_hsa_circ_218342,RMVar_hsa_circ_109449,RMVar_hsa_circ_93262,RMVar_hsa_circ_218348,RMVar_hsa_circ_54594,RMVar_hsa_circ_275888,RMVar_hsa_circ_218344,RMVar_hsa_circ_218345,RMVar_hsa_circ_218346,RMVar_hsa_circ_365390,RMVar_hsa_circ_285567,RMVar_hsa_circ_92660,RMVar_hsa_circ_114763,RMVar_hsa_circ_66297,RMVar_hsa_circ_218350,RMVar_hsa_circ_218351,RMVar_hsa_circ_218352,RMVar_hsa_circ_218349 29648 RMVar_ID_29648 Human_SNP_ID_132691580 A-to-I Human chr3 + 50097154 50097154 50097154 GCGGTGGCTCACGCCTGTAATCCCAGCACTTTAGGATTCTGAGGCAGGCGGATCACAAGGTCAGG GCGGTGGCTCACGCCTGTAATCCCAGCACTTTTGGATTCTGAGGCAGGCGGATCACAAGGTCAGG A T RBM5,RBM6 Ensembl:ENSG00000003756,Ensembl:ENSG00000004534 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs908627240 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7206163,Human_RBP_ID_14875981 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_96641,RMVar_hsa_circ_218343,RMVar_hsa_circ_6084,RMVar_hsa_circ_218342,RMVar_hsa_circ_109449,RMVar_hsa_circ_93262,RMVar_hsa_circ_218348,RMVar_hsa_circ_54594,RMVar_hsa_circ_275888,RMVar_hsa_circ_218344,RMVar_hsa_circ_218345,RMVar_hsa_circ_218346,RMVar_hsa_circ_365390,RMVar_hsa_circ_285567,RMVar_hsa_circ_92660,RMVar_hsa_circ_114763,RMVar_hsa_circ_66297,RMVar_hsa_circ_218350,RMVar_hsa_circ_218351,RMVar_hsa_circ_218352,RMVar_hsa_circ_218349 29649 RMVar_ID_29649 Human_SNP_ID_132691965 A-to-I Human chr3 + 50098789 50098789 50098789 TTGTATACAGATGGGGTCTTACTGTGTTCCCCAGGCTGGTCTCACACTCCTGTGCTCAAGCGCTC TTGTATACAGATGGGGTCTTACTGTGTTCCCCCGGCTGGTCTCACACTCCTGTGCTCAAGCGCTC A C RBM5,RBM6 Ensembl:ENSG00000003756,Ensembl:ENSG00000004534 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1365163104 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1205900 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_96641,RMVar_hsa_circ_218343,RMVar_hsa_circ_6084,RMVar_hsa_circ_218342,RMVar_hsa_circ_109449,RMVar_hsa_circ_93262,RMVar_hsa_circ_218348,RMVar_hsa_circ_54594,RMVar_hsa_circ_275888,RMVar_hsa_circ_218344,RMVar_hsa_circ_218345,RMVar_hsa_circ_218346,RMVar_hsa_circ_365390,RMVar_hsa_circ_285567,RMVar_hsa_circ_92660,RMVar_hsa_circ_114763,RMVar_hsa_circ_66297,RMVar_hsa_circ_218350,RMVar_hsa_circ_218351,RMVar_hsa_circ_218352,RMVar_hsa_circ_218349 29650 RMVar_ID_29650 Human_SNP_ID_132691980 A-to-I Human chr3 + 50098848 50098848 50098848 GCGCTCATCTTGCCTCATCTTCCCAAAGCGCTAGGATTATAGGCTTGAGCCACTGTACTATCCTG GCGCTCATCTTGCCTCATCTTCCCAAAGCGCTGGGATTATAGGCTTGAGCCACTGTACTATCCTG A G RBM5,RBM6 Ensembl:ENSG00000003756,Ensembl:ENSG00000004534 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251803818 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14876042,Human_RBP_ID_17573685 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_96641,RMVar_hsa_circ_218343,RMVar_hsa_circ_6084,RMVar_hsa_circ_218342,RMVar_hsa_circ_109449,RMVar_hsa_circ_93262,RMVar_hsa_circ_218348,RMVar_hsa_circ_54594,RMVar_hsa_circ_275888,RMVar_hsa_circ_218344,RMVar_hsa_circ_218345,RMVar_hsa_circ_218346,RMVar_hsa_circ_365390,RMVar_hsa_circ_285567,RMVar_hsa_circ_92660,RMVar_hsa_circ_114763,RMVar_hsa_circ_66297,RMVar_hsa_circ_218350,RMVar_hsa_circ_218351,RMVar_hsa_circ_218352,RMVar_hsa_circ_218349 29651 RMVar_ID_29651 Human_SNP_ID_132692031 A-to-I Human chr3 + 50099076 50099076 50099076 CAGGAGTTCCAGACCAGCCTGGGCAACGTGGCAAAACTCTGTCTCTACAAAAAATACAAAAATTA CAGGAGTTCCAGACCAGCCTGGGCAACGTGGCGAAACTCTGTCTCTACAAAAAATACAAAAATTA A G RBM5,RBM6 Ensembl:ENSG00000003756,Ensembl:ENSG00000004534 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs918259626 Functional Loss SNV dbSNP153 33..33 33 - - - 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_96641,RMVar_hsa_circ_218343,RMVar_hsa_circ_6084,RMVar_hsa_circ_218342,RMVar_hsa_circ_109449,RMVar_hsa_circ_93262,RMVar_hsa_circ_218348,RMVar_hsa_circ_54594,RMVar_hsa_circ_275888,RMVar_hsa_circ_218344,RMVar_hsa_circ_218345,RMVar_hsa_circ_218346,RMVar_hsa_circ_365390,RMVar_hsa_circ_285567,RMVar_hsa_circ_92660,RMVar_hsa_circ_114763,RMVar_hsa_circ_66297,RMVar_hsa_circ_218350,RMVar_hsa_circ_218351,RMVar_hsa_circ_218352,RMVar_hsa_circ_218349 29652 RMVar_ID_29652 Human_SNP_ID_132692060 A-to-I Human chr3 + 50099211 50099211 50099211 CAGGAAGGCAGAGGTTGCAGTGAGCTGAGATCACACCAGTGCACTTCAGCCTGGGTGTCAGAGCT CAGGAAGGCAGAGGTTGCAGTGAGCTGAGATCGCACCAGTGCACTTCAGCCTGGGTGTCAGAGCT A G RBM5,RBM6 Ensembl:ENSG00000003756,Ensembl:ENSG00000004534 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1447298140 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25743589 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_96641,RMVar_hsa_circ_218343,RMVar_hsa_circ_6084,RMVar_hsa_circ_218342,RMVar_hsa_circ_109449,RMVar_hsa_circ_93262,RMVar_hsa_circ_218348,RMVar_hsa_circ_54594,RMVar_hsa_circ_275888,RMVar_hsa_circ_218344,RMVar_hsa_circ_218345,RMVar_hsa_circ_218346,RMVar_hsa_circ_365390,RMVar_hsa_circ_285567,RMVar_hsa_circ_92660,RMVar_hsa_circ_114763,RMVar_hsa_circ_66297,RMVar_hsa_circ_218350,RMVar_hsa_circ_218351,RMVar_hsa_circ_218352,RMVar_hsa_circ_218349 29653 RMVar_ID_29653 Human_SNP_ID_132694418 A-to-I Human chr3 + 50108551 50108551 50108551 CAACATGGTGAAACCCCATCTCAGCTAAAACTACAGAAATTAGCCAGGTGCGGTGGCAGGCGCCT CAACATGGTGAAACCCCATCTCAGCTAAAACTGCAGAAATTAGCCAGGTGCGGTGGCAGGCGCCT A G RBM5 Ensembl:ENSG00000003756 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs981345971 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25771106 RMVar_hsa_circ_8277,RMVar_hsa_circ_218340,RMVar_hsa_circ_86531,RMVar_hsa_circ_93262,RMVar_hsa_circ_218344,RMVar_hsa_circ_92660,RMVar_hsa_circ_218352,RMVar_hsa_circ_38118,RMVar_hsa_circ_61152,RMVar_hsa_circ_110717,RMVar_hsa_circ_80017,RMVar_hsa_circ_60753,RMVar_hsa_circ_315215,RMVar_hsa_circ_218357,RMVar_hsa_circ_319818,RMVar_hsa_circ_116714,RMVar_hsa_circ_218360,RMVar_hsa_circ_218361,RMVar_hsa_circ_279372,RMVar_hsa_circ_299080,RMVar_hsa_circ_106827,RMVar_hsa_circ_218366,RMVar_hsa_circ_218367,RMVar_hsa_circ_282699,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_218374,RMVar_hsa_circ_218375,RMVar_hsa_circ_218373,RMVar_hsa_circ_218370,RMVar_hsa_circ_218371,RMVar_hsa_circ_218369,RMVar_hsa_circ_84806,RMVar_hsa_circ_218379 29654 RMVar_ID_29654 Human_SNP_ID_132694605 A-to-I Human chr3 + 50109255 50109255 50109255 GCCACCACTCCCGGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGA GCCACCACTCCCGGCTAATTTTTTGTATTTTTGGTAGAGACGGGGTTTCACCGTGTTAGCCAGGA A G RBM5 Ensembl:ENSG00000003756 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs568451169 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8277,RMVar_hsa_circ_218340,RMVar_hsa_circ_86531,RMVar_hsa_circ_93262,RMVar_hsa_circ_218344,RMVar_hsa_circ_92660,RMVar_hsa_circ_218352,RMVar_hsa_circ_38118,RMVar_hsa_circ_61152,RMVar_hsa_circ_110717,RMVar_hsa_circ_80017,RMVar_hsa_circ_60753,RMVar_hsa_circ_315215,RMVar_hsa_circ_218357,RMVar_hsa_circ_319818,RMVar_hsa_circ_116714,RMVar_hsa_circ_218360,RMVar_hsa_circ_218361,RMVar_hsa_circ_279372,RMVar_hsa_circ_299080,RMVar_hsa_circ_106827,RMVar_hsa_circ_218366,RMVar_hsa_circ_218367,RMVar_hsa_circ_282699,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_218374,RMVar_hsa_circ_218375,RMVar_hsa_circ_218373,RMVar_hsa_circ_218370,RMVar_hsa_circ_218371,RMVar_hsa_circ_218369,RMVar_hsa_circ_84806,RMVar_hsa_circ_218379 29655 RMVar_ID_29655 Human_SNP_ID_132695148 A-to-I Human chr3 + 50111451 50111451 50111451 TTTTTATTTTTTTTGTGGCACGATCTTGGCTCACTGCAGCCTCCACCTCCTGGGTTCAAGCAATG TTTTTATTTTTTTTGTGGCACGATCTTGGCTCGCTGCAGCCTCCACCTCCTGGGTTCAAGCAATG A G RBM5 Ensembl:ENSG00000003756 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1054068693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_782636,Human_RBP_ID_14876676 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 29656 RMVar_ID_29656 Human_SNP_ID_132695173 A-to-I Human chr3 + 50111564 50111564 50111564 CACCACACCCAGCTAATTTTTGTAGTCGAGACAGGGTTTCACCTTGTTTGCCAGGCTGGTCTCGA CACCACACCCAGCTAATTTTTGTAGTCGAGACGGGGTTTCACCTTGTTTGCCAGGCTGGTCTCGA A G RBM5 Ensembl:ENSG00000003756 Protein coding intron GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs1351686002 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7206288,Human_RBP_ID_10099082,Human_RBP_ID_14876679 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 29657 RMVar_ID_29657 Human_SNP_ID_132695369 A-to-I Human chr3 + 50112305 50112305 50112305 AAGCGTGGTGTCGAATGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCGTGAA AAGCGTGGTGTCGAATGCCTGTAGTCCCAGCTGCTCGGGAGGCTGAGGCAGGAGAATGGCGTGAA A G RBM5 Ensembl:ENSG00000003756 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1316504797 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 29658 RMVar_ID_29658 Human_SNP_ID_132695582 A-to-I Human chr3 + 50112949 50112949 50112949 ATCTTGGCTCACTGCCACCTCCTCCATCTCCCAGGTTCAAGCAGTTCTCTTGCCTCAGCCTCCTG ATCTTGGCTCACTGCCACCTCCTCCATCTCCCGGGTTCAAGCAGTTCTCTTGCCTCAGCCTCCTG A G RBM5 Ensembl:ENSG00000003756 Protein coding intron GSE47997;GSE100210;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;HepG2 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,29129909,31158229,32596459 RNA-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 29659 RMVar_ID_29659 Human_SNP_ID_132695596 A-to-I Human chr3 + 50112995 50112995 50112995 CTCTTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGTGTGCCATCATGCCCAGCTAATTTTTGT CTCTTGCCTCAGCCTCCTGAGTAGCTGGGATTGCAGGTGTGCCATCATGCCCAGCTAATTTTTGT A G RBM5 Ensembl:ENSG00000003756 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1407676572 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 29660 RMVar_ID_29660 Human_SNP_ID_132695602 A-to-I Human chr3 + 50113015 50113015 50113015 GTAGCTGGGATTACAGGTGTGCCATCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGATGAGTT GTAGCTGGGATTACAGGTGTGCCATCATGCCCGGCTAATTTTTGTATTTTTAGTAGAGATGAGTT A G RBM5 Ensembl:ENSG00000003756 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs939278629 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14876754 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 29661 RMVar_ID_29661 Human_SNP_ID_132727969 A-to-I Human chr3 + 50240858 50240858 50240858 CGAGAATCGCTTGAACCTGGGAAGTGAAGGTTACAGTGGACCGAGATGGTGCCACTGCACTCCAG CGAGAATCGCTTGAACCTGGGAAGTGAAGGTTGCAGTGGACCGAGATGGTGCCACTGCACTCCAG A G GNAI2 Ensembl:ENSG00000114353 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1227549932 Functional Loss SNV dbSNP153 33..33 33 - - - 29662 RMVar_ID_29662 Human_SNP_ID_132737394 A-to-I Human chr3 + 50277364 50277364 50277364 CACGAGGTCAGGAGATGGAAACCATCCCGGCTAACACGGTGAAACCCCGTCTGTACTAAAAATAC CACGAGGTCAGGAGATGGAAACCATCCCGGCTGACACGGTGAAACCCCGTCTGTACTAAAAATAC A G SEMA3B Ensembl:ENSG00000012171 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1228569127 Functional Loss SNV dbSNP153 33..33 33 - - - 29663 RMVar_ID_29663 Human_SNP_ID_132745867 A-to-I Human chr3 - 50304025 50304025 50304025 CTGACCTCGTGATCTGCCACCTCGGCTTCCCAAAGTGCTAGGATTATAGGCGTGAGCCTCCGCAC CTGACCTCGTGATCTGCCACCTCGGCTTCCCACAGTGCTAGGATTATAGGCGTGAGCCTCCGCAC T G HYAL1 Ensembl:ENSG00000114378 Protein coding 5'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1381959292 Functional Loss SNV dbSNP153 33..33 33 - - - 29664 RMVar_ID_29664 Human_SNP_ID_132754582 A-to-I Human chr3 - 50332844 50332844 50332844 GTGATCCACCCGCCTCGGCCTCCCAAAGTGCTAGAATTACAGGCGTGAGCCAACGTGCCCAGCCT GTGATCCACCCGCCTCGGCCTCCCAAAGTGCTGGAATTACAGGCGTGAGCCAACGTGCCCAGCCT T C RASSF1 Ensembl:ENSG00000068028 Protein coding intron GSE38233;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;Bronchiolar epithelium,BERP35T4 cell line - 24183664,31158229 RNA-Seq:(High) rs1292502360 Functional Loss SNV dbSNP153 33..33 33 - - - 29665 RMVar_ID_29665 Human_SNP_ID_132754619 A-to-I Human chr3 - 50332994 50332994 50332994 CACCTCCCGAGTTTGAGCAATTCTCCTGCCTCAGCCTCCTAAGTAGCTGGGATTACAGGCATGTG CACCTCCCGAGTTTGAGCAATTCTCCTGCCTCGGCCTCCTAAGTAGCTGGGATTACAGGCATGTG T C RASSF1 Ensembl:ENSG00000068028 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1438972852 Functional Loss SNV dbSNP153 33..33 33 - - - 29666 RMVar_ID_29666 Human_SNP_ID_132754786 A-to-I Human chr3 - 50333668 50333668 50333668 CAAGACCAACCTGGCCAATGTGGTGAAATCCCATCTCTACTAAAAATACAAAAATTAGCCGGGTG CAAGACCAACCTGGCCAATGTGGTGAAATCCCGTCTCTACTAAAAATACAAAAATTAGCCGGGTG T C RASSF1 Ensembl:ENSG00000068028 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,31158229,32596459 RNA-Seq:(High) rs1373980483 Functional Loss SNV dbSNP153 33..33 33 - - - 29667 RMVar_ID_29667 Human_SNP_ID_132754787 A-to-I Human chr3 - 50333668 50333668 50333668 CAAGACCAACCTGGCCAATGTGGTGAAATCCCATCTCTACTAAAAATACAAAAATTAGCCGGGTG CAAGACCAACCTGGCCAATGTGGTGAAATCCCCTCTCTACTAAAAATACAAAAATTAGCCGGGTG T G RASSF1 Ensembl:ENSG00000068028 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,31158229,32596459 RNA-Seq:(High) rs1373980483 Functional Loss SNV dbSNP153 33..33 33 - - - 29668 RMVar_ID_29668 Human_SNP_ID_132754796 A-to-I Human chr3 - 50333698 50333698 50333698 AGGCAGGCGGATCACTTGAGGTCAGGAGTTCAAGACCAACCTGGCCAATGTGGTGAAATCCCATC AGGCAGGCGGATCACTTGAGGTCAGGAGTTCAGGACCAACCTGGCCAATGTGGTGAAATCCCATC T C RASSF1 Ensembl:ENSG00000068028 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1288812187 Functional Loss SNV dbSNP153 33..33 33 - - - 29669 RMVar_ID_29669 Human_SNP_ID_132755088 A-to-I Human chr3 - 50335025 50335025 50335025 GAATTGCTTGAACCCAGGAGGCAGAGATTGCAATGAGCCAAGATCGCACCACTGCACTCCAGCCT GAATTGCTTGAACCCAGGAGGCAGAGATTGCAGTGAGCCAAGATCGCACCACTGCACTCCAGCCT T C RASSF1 Ensembl:ENSG00000068028 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1033780443 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14877666 29670 RMVar_ID_29670 Human_SNP_ID_132755101 A-to-I Human chr3 - 50335086 50335086 50335086 AAATTAGCCAGTTGTGGTGGCAGGCACCTGTAATCCCAGCTACTTGGGAGGCTGAAGCAGAGAAT AAATTAGCCAGTTGTGGTGGCAGGCACCTGTAGTCCCAGCTACTTGGGAGGCTGAAGCAGAGAAT T C RASSF1 Ensembl:ENSG00000068028 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1021071231 Functional Loss SNV dbSNP153 33..33 33 - - - 29671 RMVar_ID_29671 Human_SNP_ID_132755343 A-to-I Human chr3 - 50335809 50335809 50335809 TTGCAATCAGGAATTCGAGGTCAGCCTGGCCAACATGGTGAAACCCTATCTCTACTAAACATACA TTGCAATCAGGAATTCGAGGTCAGCCTGGCCACCATGGTGAAACCCTATCTCTACTAAACATACA T G RASSF1 Ensembl:ENSG00000068028 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs748549057 Functional Loss SNV dbSNP153 33..33 33 - - - 29672 RMVar_ID_29672 Human_SNP_ID_132755355 A-to-I Human chr3 - 50335872 50335872 50335872 GCCAAGTACGGTGGCTCACACCTCTAATGCCAATGCTTTGGGAGGCCAAGGCAGGTGGATCATTT GCCAAGTACGGTGGCTCACACCTCTAATGCCAGTGCTTTGGGAGGCCAAGGCAGGTGGATCATTT T C RASSF1 Ensembl:ENSG00000068028 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs587708506 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14877678 29673 RMVar_ID_29673 Human_SNP_ID_132813963 A-to-I Human chr3 - 50562024 50562024 50562024 GTGGTGGTGCACACCTGTAATCCTAGCTACTCAGGAGGCTTAGGCAGGAGAATCACTTGAACCTT GTGGTGGTGCACACCTGTAATCCTAGCTACTCGGGAGGCTTAGGCAGGAGAATCACTTGAACCTT T C C3orf18 Ensembl:ENSG00000088543 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs768159436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_157257 29674 RMVar_ID_29674 Human_SNP_ID_132845800 A-to-I Human chr3 + 50699552 50699552 50699552 TCTGCTTGCTGCAACCTCTGCCTCCTGGGTTCAGGCAGTTCTCTTGCCTCAGCCTCCTGAGTAGC TCTGCTTGCTGCAACCTCTGCCTCCTGGGTTCCGGCAGTTCTCTTGCCTCAGCCTCCTGAGTAGC A C DOCK3 Ensembl:ENSG00000088538 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1332307855 Functional Loss SNV dbSNP153 33..33 33 - - - 29675 RMVar_ID_29675 Human_SNP_ID_132884423 A-to-I Human chr3 + 50869483 50869483 50869483 ACCTCTGCCTGCTAGGCTCAAGTGATTCTCCCACCTCAGCCTCCCGAGTAGCTGGGACCACAGGT ACCTCTGCCTGCTAGGCTCAAGTGATTCTCCCGCCTCAGCCTCCCGAGTAGCTGGGACCACAGGT A G DOCK3 Ensembl:ENSG00000088538 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1462653331 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3078,RMVar_hsa_circ_343109,RMVar_hsa_circ_306939,RMVar_hsa_circ_340370,RMVar_hsa_circ_51773 29676 RMVar_ID_29676 Human_SNP_ID_132952143 A-to-I Human chr3 + 51151379 51151375 51151379 CCTGACTGTTAAAAGGAAAACTAACAAACAGAAAGGAAGAGCATCAACATCAACCAAAAGGACAT CCTGACTGTTAAAAGGAAAACTAACAAAC____AGGAAGAGCATCAACATCAACCAAAAGGACAT CAGAA C DOCK3 Ensembl:ENSG00000088538 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs932331589 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_15119,RMVar_hsa_circ_36420,RMVar_hsa_circ_334112,RMVar_hsa_circ_21612,RMVar_hsa_circ_5586,RMVar_hsa_circ_16465,RMVar_hsa_circ_218460,RMVar_hsa_circ_218461,RMVar_hsa_circ_278981 29677 RMVar_ID_29677 Human_SNP_ID_132955136 A-to-I Human chr3 + 51164535 51164535 51164535 GTCCCAGCTACTTGGGAAGGCCGAGGCAGGAGAATGGCGTGAACCCGGGAGGCAGAACTTGTAGT GTCCCAGCTACTTGGGAAGGCCGAGGCAGGAGGATGGCGTGAACCCGGGAGGCAGAACTTGTAGT A G DOCK3 Ensembl:ENSG00000088538 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs192113704 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15119,RMVar_hsa_circ_36420,RMVar_hsa_circ_29259,RMVar_hsa_circ_336026 29678 RMVar_ID_29678 Human_SNP_ID_132955658 A-to-I Human chr3 + 51166737 51166737 51166737 GATGGTTGGTGATATTGAGTACCTTTTCATATACCTGTTGGCCATTTGTGTGTCTTCTTTGGGAA GATGGTTGGTGATATTGAGTACCTTTTCATATGCCTGTTGGCCATTTGTGTGTCTTCTTTGGGAA A G DOCK3 Ensembl:ENSG00000088538 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs764018210 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15119,RMVar_hsa_circ_36420,RMVar_hsa_circ_29259,RMVar_hsa_circ_336026 29679 RMVar_ID_29679 Human_SNP_ID_132956018 A-to-I Human chr3 + 51168604 51168604 51168604 ACCATATACAAAAATCAACTCAAGATGGATTAAAGACTTAAGCATGAAACCCGAAACTATAAAAA ACCATATACAAAAATCAACTCAAGATGGATTACAGACTTAAGCATGAAACCCGAAACTATAAAAA A C DOCK3 Ensembl:ENSG00000088538 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1468960560 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15119,RMVar_hsa_circ_36420,RMVar_hsa_circ_29259,RMVar_hsa_circ_336026 29680 RMVar_ID_29680 Human_SNP_ID_133016391 A-to-I Human chr3 - 51415310 51415310 51415310 TTTTGTATTTTTGTAGAGACGGCATTTCCCCAACGTTGCCCAGGCTGGTCTCGAACTCCTGGGCT TTTTGTATTTTTGTAGAGACGGCATTTCCCCAGCGTTGCCCAGGCTGGTCTCGAACTCCTGGGCT T C DCAF1 Ensembl:ENSG00000145041 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1264522276 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_218498,RMVar_hsa_circ_59445,RMVar_hsa_circ_14115,RMVar_hsa_circ_332287,RMVar_hsa_circ_108208,RMVar_hsa_circ_269800 29681 RMVar_ID_29681 Human_SNP_ID_133016422 A-to-I Human chr3 - 51415435 51415435 51415435 GCTGCAGTGCAGTGGCACGATCACAGCTCACCACAGCCTTGACTGCCTGGACTCAAGCAATCCTC GCTGCAGTGCAGTGGCACGATCACAGCTCACCCCAGCCTTGACTGCCTGGACTCAAGCAATCCTC T G DCAF1 Ensembl:ENSG00000145041 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1217790196 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_218498,RMVar_hsa_circ_59445,RMVar_hsa_circ_14115,RMVar_hsa_circ_332287,RMVar_hsa_circ_108208,RMVar_hsa_circ_269800 29682 RMVar_ID_29682 Human_SNP_ID_133016481 A-to-I Human chr3 - 51415728 51415728 51415728 AAAATTGGCTGAGCTTGGTGGGCTTGGGACCTATAGTCCCAGCTACTCAGGAAGCTGAGACGGGA AAAATTGGCTGAGCTTGGTGGGCTTGGGACCTGTAGTCCCAGCTACTCAGGAAGCTGAGACGGGA T C DCAF1 Ensembl:ENSG00000145041 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1553630155 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_218498,RMVar_hsa_circ_59445,RMVar_hsa_circ_14115,RMVar_hsa_circ_332287,RMVar_hsa_circ_108208,RMVar_hsa_circ_269800 29683 RMVar_ID_29683 Human_SNP_ID_133018919 A-to-I Human chr3 - 51425308 51425286 51425308 ACCACCAAGCCCAGCTACTTTTTGCATTTTTTAGTAGAGACGGGGTTTTGCCATGTTGGCCAGGC ACCACCAAGCCCAGCTACTTTTTGCATTTTTT______________________GTTGGCCAGGC CATGGCAAAACCCCGTCTCTACT C DCAF1 Ensembl:ENSG00000145041 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1196069987 Functional Loss DEL dbSNP153 33..54 33 - - - RMVar_hsa_circ_59445,RMVar_hsa_circ_50678,RMVar_hsa_circ_58271,RMVar_hsa_circ_50598,RMVar_hsa_circ_34715 29684 RMVar_ID_29684 Human_SNP_ID_133019210 A-to-I Human chr3 - 51426447 51426447 51426447 TCAGCACTTTGGAAGGACGAGGTGGGCAGATCACTTGAGGTCCGAAGTTTGAGACCAGCCTGGGC TCAGCACTTTGGAAGGACGAGGTGGGCAGATCCCTTGAGGTCCGAAGTTTGAGACCAGCCTGGGC T G DCAF1 Ensembl:ENSG00000145041 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs998129773 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59445,RMVar_hsa_circ_50678,RMVar_hsa_circ_58271,RMVar_hsa_circ_50598,RMVar_hsa_circ_34715 29685 RMVar_ID_29685 Human_SNP_ID_133019655 A-to-I Human chr3 - 51428401 51428401 51428401 AGGATCATTTGAACCCAGGAGTTCAAGACTGCAGTGAGCTACGATCATATCACTGCACTCCAGTC AGGATCATTTGAACCCAGGAGTTCAAGACTGCGGTGAGCTACGATCATATCACTGCACTCCAGTC T C DCAF1 Ensembl:ENSG00000145041 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1229268814 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59445,RMVar_hsa_circ_50678,RMVar_hsa_circ_58271,RMVar_hsa_circ_50598,RMVar_hsa_circ_34715,RMVar_hsa_circ_35847,RMVar_hsa_circ_71209,RMVar_hsa_circ_348837,RMVar_hsa_circ_332963,RMVar_hsa_circ_52239,RMVar_hsa_circ_23451 29686 RMVar_ID_29686 Human_SNP_ID_133020517 A-to-I Human chr3 - 51431914 51431914 51431914 TAGGCTGTAGTGCAGTGGTGTGATCACAGCCCACTGTAGCCTTGACCTCCTGGGCTCAAGCCATC TAGGCTGTAGTGCAGTGGTGTGATCACAGCCCGCTGTAGCCTTGACCTCCTGGGCTCAAGCCATC T C DCAF1 Ensembl:ENSG00000145041 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1267325754 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59445,RMVar_hsa_circ_50678,RMVar_hsa_circ_58271,RMVar_hsa_circ_50598,RMVar_hsa_circ_3200,RMVar_hsa_circ_34715,RMVar_hsa_circ_35847,RMVar_hsa_circ_71209,RMVar_hsa_circ_348837,RMVar_hsa_circ_52239,RMVar_hsa_circ_23451,RMVar_hsa_circ_320376,RMVar_hsa_circ_63151,RMVar_hsa_circ_31441 29687 RMVar_ID_29687 Human_SNP_ID_133022696 A-to-I Human chr3 - 51440551 51440551 51440551 TCACCCAGGCTGGAGTGCAATGGGGTGATCATAGCTCACTGTGGCTTTGAACTCCTAGGCCCAAG TCACCCAGGCTGGAGTGCAATGGGGTGATCATTGCTCACTGTGGCTTTGAACTCCTAGGCCCAAG T A DCAF1 Ensembl:ENSG00000145041 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs533282215 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14881810 RMVar_hsa_circ_59445,RMVar_hsa_circ_58271,RMVar_hsa_circ_50598,RMVar_hsa_circ_3200,RMVar_hsa_circ_34715,RMVar_hsa_circ_71209,RMVar_hsa_circ_348837,RMVar_hsa_circ_52239,RMVar_hsa_circ_23451,RMVar_hsa_circ_63151,RMVar_hsa_circ_57440,RMVar_hsa_circ_31441,RMVar_hsa_circ_286581,RMVar_hsa_circ_34996 29688 RMVar_ID_29688 Human_SNP_ID_133026197 A-to-I Human chr3 - 51454121 51454121 51454121 GGAGGATCGCTTCAACTCAGGAAGTAGAGGCTATGGTTAGCCCTGATCGTGCTGCCGCACTCCAG GGAGGATCGCTTCAACTCAGGAAGTAGAGGCTGTGGTTAGCCCTGATCGTGCTGCCGCACTCCAG T C DCAF1 Ensembl:ENSG00000145041 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1175857763 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14881921 RMVar_hsa_circ_59445,RMVar_hsa_circ_58271,RMVar_hsa_circ_50598,RMVar_hsa_circ_36808,RMVar_hsa_circ_80968,RMVar_hsa_circ_23451,RMVar_hsa_circ_31441,RMVar_hsa_circ_360722,RMVar_hsa_circ_34996,RMVar_hsa_circ_373975,RMVar_hsa_circ_341585,RMVar_hsa_circ_310475,RMVar_hsa_circ_89554,RMVar_hsa_circ_218510,RMVar_hsa_circ_13970,RMVar_hsa_circ_218511,RMVar_hsa_circ_218512,RMVar_hsa_circ_218508,RMVar_hsa_circ_218509,RMVar_hsa_circ_45759 29689 RMVar_ID_29689 Human_SNP_ID_133028884 A-to-I Human chr3 - 51463969 51463969 51463969 GCACCTGTGGTCCCAGCTACTTGGGAGGCTGAAGCTGGAGGATCACTTGAGACTGGGAGGTCGAG GCACCTGTGGTCCCAGCTACTTGGGAGGCTGACGCTGGAGGATCACTTGAGACTGGGAGGTCGAG T G DCAF1 Ensembl:ENSG00000145041 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs970291325 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59445,RMVar_hsa_circ_58271,RMVar_hsa_circ_50598,RMVar_hsa_circ_36808,RMVar_hsa_circ_80968,RMVar_hsa_circ_23451,RMVar_hsa_circ_31441,RMVar_hsa_circ_360722,RMVar_hsa_circ_34996,RMVar_hsa_circ_341585,RMVar_hsa_circ_310475,RMVar_hsa_circ_89554,RMVar_hsa_circ_218510,RMVar_hsa_circ_13970,RMVar_hsa_circ_218511,RMVar_hsa_circ_218512,RMVar_hsa_circ_218509,RMVar_hsa_circ_45759,RMVar_hsa_circ_218513,RMVar_hsa_circ_14826,RMVar_hsa_circ_271332,RMVar_hsa_circ_271657,RMVar_hsa_circ_346011,RMVar_hsa_circ_39356,RMVar_hsa_circ_218514,RMVar_hsa_circ_218515 29690 RMVar_ID_29690 Human_SNP_ID_133030291 A-to-I Human chr3 - 51469912 51469912 51469912 GGTTCAAGCAATTTTTGTGCCTCAGTGTCCCAAGTAGCTGGGATTACAAGCATGCACCACCACAG GGTTCAAGCAATTTTTGTGCCTCAGTGTCCCAGGTAGCTGGGATTACAAGCATGCACCACCACAG T C DCAF1 Ensembl:ENSG00000145041 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1401786108 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59445,RMVar_hsa_circ_58271,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_89554,RMVar_hsa_circ_218510,RMVar_hsa_circ_13970,RMVar_hsa_circ_218511,RMVar_hsa_circ_218512,RMVar_hsa_circ_45759,RMVar_hsa_circ_14826,RMVar_hsa_circ_271332,RMVar_hsa_circ_346011,RMVar_hsa_circ_39356,RMVar_hsa_circ_218514,RMVar_hsa_circ_218515,RMVar_hsa_circ_218516,RMVar_hsa_circ_361291 29691 RMVar_ID_29691 Human_SNP_ID_133032382 A-to-I Human chr3 - 51478058 51478058 51478058 TCGAGGCTGCAGTGAGCTGAGATTGTGCCACTACACTCCAGCCTGGGCAAGAGAGACTCTGTCTC TCGAGGCTGCAGTGAGCTGAGATTGTGCCACTGCACTCCAGCCTGGGCAAGAGAGACTCTGTCTC T C DCAF1 Ensembl:ENSG00000145041 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1454542042 Functional Loss SNV dbSNP153 33..33 33 - - - 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 29692 RMVar_ID_29692 Human_SNP_ID_133032833 A-to-I Human chr3 - 51479867 51479867 51479867 CACCACTTTGTTTTAATACTCCTGTCATTCATATGTATGTATTTTAATTTTCCCCCATTATACCA CACCACTTTGTTTTAATACTCCTGTCATTCATGTGTATGTATTTTAATTTTCCCCCATTATACCA T C DCAF1 Ensembl:ENSG00000145041 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1193596917 Functional Loss SNV dbSNP153 33..33 33 - - - 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 29693 RMVar_ID_29693 Human_SNP_ID_133033146 A-to-I Human chr3 - 51481029 51481029 51481029 CCAGTGACCTTCTCCTTAGAAAACCCATGAGCACCTCTACCCAGCCTTTACTTTTCACTCTTTCT CCAGTGACCTTCTCCTTAGAAAACCCATGAGCGCCTCTACCCAGCCTTTACTTTTCACTCTTTCT T C DCAF1 Ensembl:ENSG00000145041 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1258036702 Functional Loss SNV dbSNP153 33..33 33 - - - 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 29694 RMVar_ID_29694 Human_SNP_ID_133033150 A-to-I Human chr3 - 51481044 51481044 51481044 GAGGATTCCCACGTTCCAGTGACCTTCTCCTTAGAAAACCCATGAGCACCTCTACCCAGCCTTTA GAGGATTCCCACGTTCCAGTGACCTTCTCCTTGGAAAACCCATGAGCACCTCTACCCAGCCTTTA T C DCAF1 Ensembl:ENSG00000145041 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1482260451 Functional Loss SNV dbSNP153 33..33 33 - - - 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 29695 RMVar_ID_29695 Human_SNP_ID_133034675 A-to-I Human chr3 - 51486095 51486095 51486095 ATGAGGTCAGGAGATTGAGACCATCCTGGCTAACACGGTGAAAGCCCGTCTCTCCTAAAAATACA ATGAGGTCAGGAGATTGAGACCATCCTGGCTACCACGGTGAAAGCCCGTCTCTCCTAAAAATACA T G DCAF1 Ensembl:ENSG00000145041 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1220955975 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59445,RMVar_hsa_circ_80968,RMVar_hsa_circ_23451,RMVar_hsa_circ_31441,RMVar_hsa_circ_360722,RMVar_hsa_circ_13970,RMVar_hsa_circ_218512,RMVar_hsa_circ_14826,RMVar_hsa_circ_39356,RMVar_hsa_circ_300256,RMVar_hsa_circ_305308,RMVar_hsa_circ_218517,RMVar_hsa_circ_218518,RMVar_hsa_circ_321888,RMVar_hsa_circ_353200 29696 RMVar_ID_29696 Human_SNP_ID_133034781 A-to-I Human chr3 - 51486473 51486473 51486473 GTCTGAAAATATGGCGGGGTGTGGTGGCTCACACCTGTTGTCTCAGCACTTTGGGGGGCTAAGGC GTCTGAAAATATGGCGGGGTGTGGTGGCTCACCCCTGTTGTCTCAGCACTTTGGGGGGCTAAGGC T G DCAF1 Ensembl:ENSG00000145041 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1302888891 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14882195 RMVar_hsa_circ_59445,RMVar_hsa_circ_80968,RMVar_hsa_circ_23451,RMVar_hsa_circ_31441,RMVar_hsa_circ_360722,RMVar_hsa_circ_13970,RMVar_hsa_circ_218512,RMVar_hsa_circ_14826,RMVar_hsa_circ_39356,RMVar_hsa_circ_300256,RMVar_hsa_circ_305308,RMVar_hsa_circ_218517,RMVar_hsa_circ_218518,RMVar_hsa_circ_321888,RMVar_hsa_circ_353200 29697 RMVar_ID_29697 Human_SNP_ID_133036235 A-to-I Human chr3 - 51491592 51491592 51491592 TGCCTGTCTTGGCCTCCCAAAGTGCAGGGATTACAGGCATGAGCCACTGCACCTGGGCAGCACTA TGCCTGTCTTGGCCTCCCAAAGTGCAGGGATTGCAGGCATGAGCCACTGCACCTGGGCAGCACTA T C DCAF1 Ensembl:ENSG00000145041 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1553657975 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23189837 RMVar_hsa_circ_59445,RMVar_hsa_circ_80968,RMVar_hsa_circ_23451,RMVar_hsa_circ_31441,RMVar_hsa_circ_360722,RMVar_hsa_circ_13970,RMVar_hsa_circ_218512,RMVar_hsa_circ_14826,RMVar_hsa_circ_39356,RMVar_hsa_circ_300256,RMVar_hsa_circ_305308,RMVar_hsa_circ_218517,RMVar_hsa_circ_218518,RMVar_hsa_circ_321888,RMVar_hsa_circ_353200 29698 RMVar_ID_29698 Human_SNP_ID_133036500 A-to-I Human chr3 - 51492469 51492469 51492469 TCCTTTTGCCCAGGCCGGTGTGCATTGGGGTAATCTCGGCTGACTGCAACCTCCGTCCCCTCCGA TCCTTTTGCCCAGGCCGGTGTGCATTGGGGTACTCTCGGCTGACTGCAACCTCCGTCCCCTCCGA T G DCAF1 Ensembl:ENSG00000145041 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1315437874 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_933797,Human_RBP_ID_4748350,Human_RBP_ID_14882359,Human_RBP_ID_24009856 RMVar_hsa_circ_59445,RMVar_hsa_circ_80968,RMVar_hsa_circ_23451,RMVar_hsa_circ_31441,RMVar_hsa_circ_360722,RMVar_hsa_circ_13970,RMVar_hsa_circ_218512,RMVar_hsa_circ_14826,RMVar_hsa_circ_39356,RMVar_hsa_circ_300256,RMVar_hsa_circ_305308,RMVar_hsa_circ_218517,RMVar_hsa_circ_218518,RMVar_hsa_circ_321888,RMVar_hsa_circ_353200 29699 RMVar_ID_29699 Human_SNP_ID_133037274 A-to-I Human chr3 - 51495237 51495237 51495237 TCACTGCAACTTCTGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTGGCTGGGA TCACTGCAACTTCTGCCTCCCGGGTTCAAGCGGTTCTCCTGCCTCAGCCTCCCGAGTGGCTGGGA T C DCAF1 Ensembl:ENSG00000145041 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1553660156 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59445,RMVar_hsa_circ_80968,RMVar_hsa_circ_360722,RMVar_hsa_circ_218512,RMVar_hsa_circ_39356,RMVar_hsa_circ_300256,RMVar_hsa_circ_218517,RMVar_hsa_circ_353200 29700 RMVar_ID_29700 Human_SNP_ID_133050267 A-to-I Human chr3 + 51546433 51546433 51546433 GAGGCTGAGGCGGGCGGATCACCTGATGTCGGAAGTTTGAGACCAGCCTGATCAACATGGAGAAA GAGGCTGAGGCGGGCGGATCACCTGATGTCGGGAGTTTGAGACCAGCCTGATCAACATGGAGAAA A G RAD54L2 Ensembl:ENSG00000164080 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1456137554 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6574,RMVar_hsa_circ_46093,RMVar_hsa_circ_275948,RMVar_hsa_circ_35181,RMVar_hsa_circ_17963,RMVar_hsa_circ_77304,RMVar_hsa_circ_83899,RMVar_hsa_circ_100722,RMVar_hsa_circ_102227,RMVar_hsa_circ_218522,RMVar_hsa_circ_218524,RMVar_hsa_circ_218525,RMVar_hsa_circ_218523,RMVar_hsa_circ_96898,RMVar_hsa_circ_285094,RMVar_hsa_circ_218526,RMVar_hsa_circ_218527,RMVar_hsa_circ_316608,RMVar_hsa_circ_334342,RMVar_hsa_circ_348176,RMVar_hsa_circ_309658,RMVar_hsa_circ_44751,RMVar_hsa_circ_51286,RMVar_hsa_circ_35260,RMVar_hsa_circ_218528,RMVar_hsa_circ_218529 29701 RMVar_ID_29701 Human_SNP_ID_133052015 A-to-I Human chr3 + 51553555 51553555 51553555 ACATATAAAAGTTATGTGTACAGGCTTGGCATAGTTGCTTATGTCCGTAATTCCAGTACTTTGGG ACATATAAAAGTTATGTGTACAGGCTTGGCATTGTTGCTTATGTCCGTAATTCCAGTACTTTGGG A T RAD54L2 Ensembl:ENSG00000164080 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1366137881 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6574,RMVar_hsa_circ_46093,RMVar_hsa_circ_275948,RMVar_hsa_circ_35181,RMVar_hsa_circ_17963,RMVar_hsa_circ_77304,RMVar_hsa_circ_100722,RMVar_hsa_circ_102227,RMVar_hsa_circ_218524,RMVar_hsa_circ_218525,RMVar_hsa_circ_218523,RMVar_hsa_circ_96898,RMVar_hsa_circ_285094,RMVar_hsa_circ_218526,RMVar_hsa_circ_218527,RMVar_hsa_circ_316608,RMVar_hsa_circ_334342,RMVar_hsa_circ_348176,RMVar_hsa_circ_309658,RMVar_hsa_circ_44751,RMVar_hsa_circ_51286,RMVar_hsa_circ_35260,RMVar_hsa_circ_218528,RMVar_hsa_circ_218529 29702 RMVar_ID_29702 Human_SNP_ID_133079274 A-to-I Human chr3 - 51668056 51668056 51668056 ACTCACACACACACACACACACAGCTGGGCTGAGCTCTCTTCCAGGGAGGGTCCTGGGTCCAGTC ACTCACACACACACACACACACAGCTGGGCTGGGCTCTCTTCCAGGGAGGGTCCTGGGTCCAGTC T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs959044363 Functional Loss SNV dbSNP153 33..33 33 - - - 29703 RMVar_ID_29703 Human_SNP_ID_133151649 A-to-I Human chr3 - 51972324 51972324 51972324 CTCAGGTGATCCGCCCGCCTCGGCCTCCCAAAATGCTGGGATTACAGGCGTGTGCCACCGCGCCT CTCAGGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGTGCCACCGCGCCT T C PCBP4,ABHD14B,AC115284.1 Ensembl:ENSG00000090097,Ensembl:ENSG00000114779,Ensembl:ENSG00000272762 Protein coding,Protein coding,lincRNA intron,intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1339891221 Functional Loss SNV dbSNP153 33..33 33 - - - 29704 RMVar_ID_29704 Human_SNP_ID_133151708 A-to-I Human chr3 - 51972534 51972534 51972534 AGTTTTTCTCTTGTTGCCCAGTCTGGAGTGCAATGGCGCGTTCTCGGCTCACTGCAACCTCTGCC AGTTTTTCTCTTGTTGCCCAGTCTGGAGTGCAGTGGCGCGTTCTCGGCTCACTGCAACCTCTGCC T C PCBP4,ABHD14B,AC115284.1 Ensembl:ENSG00000090097,Ensembl:ENSG00000114779,Ensembl:ENSG00000272762 Protein coding,Protein coding,lincRNA intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs573019183 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14885843 29705 RMVar_ID_29705 Human_SNP_ID_133153487 A-to-I Human chr3 - 51978811 51978811 51978811 GAGGCAGGCGAATCACCTGAGGTCGGGAGTTCAGGACCAGCCTGGCCAGCATGGTGAAACCCTAT GAGGCAGGCGAATCACCTGAGGTCGGGAGTTCGGGACCAGCCTGGCCAGCATGGTGAAACCCTAT T C ABHD14B Ensembl:ENSG00000114779 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1320579399 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14885875 29706 RMVar_ID_29706 Human_SNP_ID_133172803 A-to-I Human chr3 - 52049528 52049528 52049528 CTTGCCCTGCCCTCATCTTGCCCATGCCTTCTACTGCCAGGAGACTTGCACCCATTTCAACCCTA CTTGCCCTGCCCTCATCTTGCCCATGCCTTCTTCTGCCAGGAGACTTGCACCCATTTCAACCCTA T A DUSP7 Ensembl:ENSG00000164086 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs909489881 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18954394,Human_RBP_ID_20920148,Human_RBP_ID_26510427,Human_RBP_ID_27503672 RMVar_hsa_circ_87323,RMVar_hsa_circ_218589 29707 RMVar_ID_29707 Human_SNP_ID_133179415 A-to-I Human chr3 - 52075876 52075876 52075876 CATGCAGAGAGCAACACCATGATCAGGGGAGCAGGAATCAGGAGCTCGGTGGATTTGCAGGTGGC CATGCAGAGAGCAACACCATGATCAGGGGAGCTGGAATCAGGAGCTCGGTGGATTTGCAGGTGGC T A POC1A Ensembl:ENSG00000164087 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs747885661 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18811446 29708 RMVar_ID_29708 Human_SNP_ID_133206620 A-to-I Human chr3 + 52193473 52193473 52193473 GTCCCTTCCCCCAAGTTATCAAATCCAAGGGCAATGTTGTGAGCATCAAGGTAGACAAGGGGGTG GTCCCTTCCCCCAAGTTATCAAATCCAAGGGCGATGTTGTGAGCATCAAGGTAGACAAGGGGGTG A G ALDOAP1 Ensembl:ENSG00000242849 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879061170 Functional Loss SNV dbSNP153 33..33 33 - - - 29709 RMVar_ID_29709 Human_SNP_ID_133206624 A-to-I Human chr3 + 52193482 52193482 52193482 CCCAAGTTATCAAATCCAAGGGCAATGTTGTGAGCATCAAGGTAGACAAGGGGGTGGTACCCCTG CCCAAGTTATCAAATCCAAGGGCAATGTTGTGGGCATCAAGGTAGACAAGGGGGTGGTACCCCTG A G ALDOAP1 Ensembl:ENSG00000242849 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878949909 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1877153 29710 RMVar_ID_29710 Human_SNP_ID_133210780 A-to-I Human chr3 + 52209414 52209414 52209414 TATTTGTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGAATGTTCTCAATCTCCTGACCACGTGA TATTTGTAGTAGAGACGGGGTTTCACCGTGTTGGCCAGAATGTTCTCAATCTCCTGACCACGTGA A G ALAS1 Ensembl:ENSG00000023330 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1166240998 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34967,RMVar_hsa_circ_87445,RMVar_hsa_circ_316299,RMVar_hsa_circ_108035,RMVar_hsa_circ_218604,RMVar_hsa_circ_218605,RMVar_hsa_circ_218603 29711 RMVar_ID_29711 Human_SNP_ID_133211086 A-to-I Human chr3 + 52210728 52210728 52210728 TTGAGCCCAGGAGGTTGAGGCTGCAGAGAGCTATGATCATGCCACTGCACTCCAGCCTGGGTGAC TTGAGCCCAGGAGGTTGAGGCTGCAGAGAGCTGTGATCATGCCACTGCACTCCAGCCTGGGTGAC A G ALAS1 Ensembl:ENSG00000023330 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs377110072 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34967,RMVar_hsa_circ_87445,RMVar_hsa_circ_316299,RMVar_hsa_circ_108035,RMVar_hsa_circ_218604,RMVar_hsa_circ_218605,RMVar_hsa_circ_218603 29712 RMVar_ID_29712 Human_SNP_ID_133226540 A-to-I Human chr3 - 52268990 52268990 52268990 GGCAACTTGGGAAAACCCCGTCTCTACAAAAAATACAAAAATTAGCCAGGTGTGATGGGACGCGC GGCAACTTGGGAAAACCCCGTCTCTACAAAAATTACAAAAATTAGCCAGGTGTGATGGGACGCGC T A WDR82 Ensembl:ENSG00000164091 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1353994320 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14889130 RMVar_hsa_circ_116751,RMVar_hsa_circ_218622,RMVar_hsa_circ_107672,RMVar_hsa_circ_218621,RMVar_hsa_circ_347539,RMVar_hsa_circ_309383,RMVar_hsa_circ_344945,RMVar_hsa_circ_351051,RMVar_hsa_circ_359369 29713 RMVar_ID_29713 Human_SNP_ID_133226864 A-to-I Human chr3 - 52270260 52270260 52270260 CAGAAGTTAGCTGGGCACAGTGGTGCACGCCTATAATCCCAGCTACACAGGAGGCTGAGGCAGGA CAGAAGTTAGCTGGGCACAGTGGTGCACGCCTGTAATCCCAGCTACACAGGAGGCTGAGGCAGGA T C WDR82 Ensembl:ENSG00000164091 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1417125273 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116751,RMVar_hsa_circ_218622,RMVar_hsa_circ_107672,RMVar_hsa_circ_218621,RMVar_hsa_circ_347539,RMVar_hsa_circ_309383,RMVar_hsa_circ_344945,RMVar_hsa_circ_351051,RMVar_hsa_circ_359369 29714 RMVar_ID_29714 Human_SNP_ID_133227273 A-to-I Human chr3 - 52272007 52272007 52272007 TGGCTTACTGCAACCTCTGCCTCCTGGGTTCAAGGAATTCTCCTGCCTCAGCCTCTTGAGTAGCT TGGCTTACTGCAACCTCTGCCTCCTGGGTTCAGGGAATTCTCCTGCCTCAGCCTCTTGAGTAGCT T C WDR82 Ensembl:ENSG00000164091 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs568062609 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107672,RMVar_hsa_circ_218621 29715 RMVar_ID_29715 Human_SNP_ID_133227754 A-to-I Human chr3 - 52273795 52273795 52273795 AATGTGGTGAAACCTTGTCTATACAGAAAAATACAAAAATTAGCTGAGCCTGGTGGCAGGGGCCT AATGTGGTGAAACCTTGTCTATACAGAAAAATGCAAAAATTAGCTGAGCCTGGTGGCAGGGGCCT T C WDR82 Ensembl:ENSG00000164091 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1287833871 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107672,RMVar_hsa_circ_218621 29716 RMVar_ID_29716 Human_SNP_ID_133230288 A-to-I Human chr3 - 52282920 52282920 52282920 TTTCTTTTTTTTTTGAGACAGAGTTTCACTCTATCGCCCAGGCTGGAGTGCGATCTCGGCTCTGC TTTCTTTTTTTTTTGAGACAGAGTTTCACTCTGTCGCCCAGGCTGGAGTGCGATCTCGGCTCTGC T C WDR82 Ensembl:ENSG00000164091 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1052250215 Functional Loss SNV dbSNP153 33..33 33 - - - 29717 RMVar_ID_29717 Human_SNP_ID_133268025 A-to-I Human chr3 + 52415245 52415245 52415245 TGAGAACGGAGTCTCACTCTCTTGCCCAGGCTAGAGTGCAGTGGCGTGATCCCGGCTCACTGCAA TGAGAACGGAGTCTCACTCTCTTGCCCAGGCTGGAGTGCAGTGGCGTGATCCCGGCTCACTGCAA A G PHF7 Ensembl:ENSG00000010318 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,31158229,31158229,32596459,32596459 RNA-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 29718 RMVar_ID_29718 Human_SNP_ID_133268040 A-to-I Human chr3 + 52415314 52415314 52415314 TGCCTCCCTGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGACACCTA TGCCTCCCTGGTTCAAGTGATTCTCCTGCCTCGGCCTCCCAAGTAGCTGGGATTACAGACACCTA A G PHF7 Ensembl:ENSG00000010318 Protein coding intron GSE38233;GSE107867;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;esophageal squamous carcinoma cells,EC109 cell line - 24183664,30559470,32596459 RNA-Seq:(High) rs1445691155 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 29719 RMVar_ID_29719 Human_SNP_ID_133268283 A-to-I Human chr3 + 52416358 52416351 52416359 CAGGTGCCTGTCACCACGCATGGCTAATTTTTATATTTTTAGTAGAGACAGGGTTTCACCGTGTT CAGGTGCCTGTCACCACGCATGGCTA________ATTTTTAGTAGAGACAGGGTTTCACCGTGTT AATTTTTAT A PHF7 Ensembl:ENSG00000010318 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1443788214 Functional Loss DEL dbSNP153 27..34 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 29720 RMVar_ID_29720 Human_SNP_ID_133268304 A-to-I Human chr3 + 52416444 52416444 52416444 TTGACCTCGTGATCTGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCG TTGACCTCGTGATCTGCCCACCTCGGCCTCCCGAAGTGCTGGGATTACAGGCGTGAGCCACCGCG A G PHF7 Ensembl:ENSG00000010318 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs182052065 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23189873 Clinvar_Rec_99,Clinvar_Rec_100,Clinvar_Rec_101 RMVar_hsa_circ_115233,RMVar_hsa_circ_369935,RMVar_hsa_circ_218652,RMVar_hsa_circ_218654,RMVar_hsa_circ_76878,RMVar_hsa_circ_218653 29721 RMVar_ID_29721 Human_SNP_ID_133268305 A-to-I Human chr3 + 52416445 52416445 52416445 TGACCTCGTGATCTGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGC TGACCTCGTGATCTGCCCACCTCGGCCTCCCAGAGTGCTGGGATTACAGGCGTGAGCCACCGCGC A G PHF7 Ensembl:ENSG00000010318 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1369298956 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23189873 RMVar_hsa_circ_115233,RMVar_hsa_circ_369935,RMVar_hsa_circ_218652,RMVar_hsa_circ_218654,RMVar_hsa_circ_76878,RMVar_hsa_circ_218653 29722 RMVar_ID_29722 Human_SNP_ID_133268344 A-to-I Human chr3 + 52416585 52416585 52416585 GGTCGGGCACAGTGGCTCACGCCTGTAATCCCAGAACTTTGGGAGGCCGAGGCGAGCAGATCAAG GGTCGGGCACAGTGGCTCACGCCTGTAATCCCGGAACTTTGGGAGGCCGAGGCGAGCAGATCAAG A G PHF7 Ensembl:ENSG00000010318 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1325174292 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 29723 RMVar_ID_29723 Human_SNP_ID_133268345 A-to-I Human chr3 + 52416587 52416587 52416587 TCGGGCACAGTGGCTCACGCCTGTAATCCCAGAACTTTGGGAGGCCGAGGCGAGCAGATCAAGAG TCGGGCACAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGAGCAGATCAAGAG A C PHF7 Ensembl:ENSG00000010318 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs916281101 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 29724 RMVar_ID_29724 Human_SNP_ID_133268355 A-to-I Human chr3 + 52416615 52416615 52416615 CCAGAACTTTGGGAGGCCGAGGCGAGCAGATCAAGAGGTCAGGAGATGGAGACCATCCTGGCTAA CCAGAACTTTGGGAGGCCGAGGCGAGCAGATCGAGAGGTCAGGAGATGGAGACCATCCTGGCTAA A G PHF7 Ensembl:ENSG00000010318 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1465564544 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 29725 RMVar_ID_29725 Human_SNP_ID_133280113 A-to-I Human chr3 + 52460606 52460606 52460606 AAAATTTTTTTGTAGAGATGGGGTCTTGCAGTATTGCTCAGGTTGGCCTCAAACTCGAACTCAAG AAAATTTTTTTGTAGAGATGGGGTCTTGCAGTTTTGCTCAGGTTGGCCTCAAACTCGAACTCAAG A T NISCH Ensembl:ENSG00000010322 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1280465185 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14890524 RMVar_hsa_circ_86712,RMVar_hsa_circ_118954,RMVar_hsa_circ_123033,RMVar_hsa_circ_218660,RMVar_hsa_circ_120343,RMVar_hsa_circ_218661,RMVar_hsa_circ_218662,RMVar_hsa_circ_218663 29726 RMVar_ID_29726 Human_SNP_ID_133283783 A-to-I Human chr3 + 52474684 52474684 52474684 GAACTCCTGACCTCAAGTGATCCACCAGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAG GAACTCCTGACCTCAAGTGATCCACCAGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAG A G NISCH Ensembl:ENSG00000010322 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs985239952 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86712,RMVar_hsa_circ_118954,RMVar_hsa_circ_123033,RMVar_hsa_circ_218660,RMVar_hsa_circ_120343,RMVar_hsa_circ_218661,RMVar_hsa_circ_218662,RMVar_hsa_circ_218663,RMVar_hsa_circ_218665,RMVar_hsa_circ_94297,RMVar_hsa_circ_103500,RMVar_hsa_circ_218667 29727 RMVar_ID_29727 Human_SNP_ID_133283784 A-to-I Human chr3 + 52474692 52474692 52474692 GACCTCAAGTGATCCACCAGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTTCA GACCTCAAGTGATCCACCAGCCTCAGCCTCCCGAAGTGCTGGGATTACAGGCATGAGCCACTTCA A G NISCH Ensembl:ENSG00000010322 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1303797088 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86712,RMVar_hsa_circ_118954,RMVar_hsa_circ_123033,RMVar_hsa_circ_218660,RMVar_hsa_circ_120343,RMVar_hsa_circ_218661,RMVar_hsa_circ_218662,RMVar_hsa_circ_218663,RMVar_hsa_circ_218665,RMVar_hsa_circ_94297,RMVar_hsa_circ_103500,RMVar_hsa_circ_218667 29728 RMVar_ID_29728 Human_SNP_ID_133283789 A-to-I Human chr3 + 52474708 52474708 52474708 CCAGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTTCAGCCGGCCGTCATTGGT CCAGCCTCAGCCTCCCAAAGTGCTGGGATTACGGGCATGAGCCACTTCAGCCGGCCGTCATTGGT A G NISCH Ensembl:ENSG00000010322 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs912264251 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86712,RMVar_hsa_circ_118954,RMVar_hsa_circ_123033,RMVar_hsa_circ_218660,RMVar_hsa_circ_120343,RMVar_hsa_circ_218661,RMVar_hsa_circ_218662,RMVar_hsa_circ_218663,RMVar_hsa_circ_218665,RMVar_hsa_circ_94297,RMVar_hsa_circ_103500,RMVar_hsa_circ_218667 29729 RMVar_ID_29729 Human_SNP_ID_133300538 A-to-I Human chr3 - 52525275 52525275 52525275 TCCTCTCCCTAGGGAAACCTGTTTGACTTCTTACGCTTGACGGAATGGCGTGGCCCCCGCGTGCT TCCTCTCCCTAGGGAAACCTGTTTGACTTCTTGCGCTTGACGGAATGGCGTGGCCCCCGCGTGCT T C NT5DC2 Ensembl:ENSG00000168268 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs11545651 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_70223,Human_RBP_ID_605504,Human_RBP_ID_933826,Human_RBP_ID_4749559,Human_RBP_ID_8576120,Human_RBP_ID_8875051,Human_RBP_ID_17292708,Human_RBP_ID_17404655,Human_RBP_ID_17521430,Human_RBP_ID_19010581,Human_RBP_ID_27320988 Human_Splice_Rec_438688,Human_Splice_Rec_438689,Human_Splice_Rec_438695,Human_Splice_Rec_438720,Human_Splice_Rec_438721,Human_Splice_Rec_438746,Human_Splice_Rec_438747,Human_Splice_Rec_438753,Human_Splice_Rec_438776,Human_Splice_Rec_438777,Human_Splice_Rec_438800,Human_Splice_Rec_438801,Human_Splice_Rec_438810,Human_Splice_Rec_438811,Human_Splice_Rec_438822,Human_Splice_Rec_438823 Human_miRNA_ID_1337337,Human_miRNA_ID_1354203 RMVar_hsa_circ_57122 29730 RMVar_ID_29730 Human_SNP_ID_133305597 A-to-I Human chr3 + 52543024 52543024 52543024 ATAGTTCACTGCAGCCTTGAACTCTTGGGCTCAAGCGATCCTCCTGCCTCAGCCTCCCAGGTAGC ATAGTTCACTGCAGCCTTGAACTCTTGGGCTCCAGCGATCCTCCTGCCTCAGCCTCCCAGGTAGC A C SMIM4 Ensembl:ENSG00000168273 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs574941949 Functional Loss SNV dbSNP153 33..33 33 - - - 29731 RMVar_ID_29731 Human_SNP_ID_133305707 A-to-I Human chr3 + 52543511 52543510 52543511 AGTCCCAGCTATTTGGGAGGCTGAGGTGGGAGAATCACCTGAGCCAGATCAAGACTGCAGTAAGT AGTCCCAGCTATTTGGGAGGCTGAGGTGGGAG_ATCACCTGAGCCAGATCAAGACTGCAGTAAGT GA G SMIM4 Ensembl:ENSG00000168273 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1255674527 Functional Loss DEL dbSNP153 33..33 33 - - - 29732 RMVar_ID_29732 Human_SNP_ID_133305709 A-to-I Human chr3 + 52543511 52543511 52543511 AGTCCCAGCTATTTGGGAGGCTGAGGTGGGAGAATCACCTGAGCCAGATCAAGACTGCAGTAAGT AGTCCCAGCTATTTGGGAGGCTGAGGTGGGAGGATCACCTGAGCCAGATCAAGACTGCAGTAAGT A G SMIM4 Ensembl:ENSG00000168273 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1205485701 Functional Loss SNV dbSNP153 33..33 33 - - - 29733 RMVar_ID_29733 Human_SNP_ID_133314428 A-to-I Human chr3 - 52580153 52580153 52580153 TCACTGCAAACTCCAATTGCCAGGCCCAAGCAATCTTCCTACCTCAGCCTCCCAAGTAGCTGTGA TCACTGCAAACTCCAATTGCCAGGCCCAAGCAGTCTTCCTACCTCAGCCTCCCAAGTAGCTGTGA T C PBRM1 Ensembl:ENSG00000163939 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs918996848 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_261,RMVar_hsa_circ_13769,RMVar_hsa_circ_31,RMVar_hsa_circ_341821,RMVar_hsa_circ_64282,RMVar_hsa_circ_39930,RMVar_hsa_circ_297405,RMVar_hsa_circ_342373,RMVar_hsa_circ_365721,RMVar_hsa_circ_32727,RMVar_hsa_circ_32897,RMVar_hsa_circ_3110,RMVar_hsa_circ_218708,RMVar_hsa_circ_218709,RMVar_hsa_circ_65007,RMVar_hsa_circ_304485 29734 RMVar_ID_29734 Human_SNP_ID_133314756 A-to-I Human chr3 - 52581344 52581344 52581344 CATCATGCCTGGCTAATTTTTGTATCTTTAATAGAGATGGGGTTTTACCATGTTGGCCAGTCTGG CATCATGCCTGGCTAATTTTTGTATCTTTAATGGAGATGGGGTTTTACCATGTTGGCCAGTCTGG T C PBRM1 Ensembl:ENSG00000163939 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs942663628 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_261,RMVar_hsa_circ_13769,RMVar_hsa_circ_31,RMVar_hsa_circ_341821,RMVar_hsa_circ_64282,RMVar_hsa_circ_39930,RMVar_hsa_circ_297405,RMVar_hsa_circ_342373,RMVar_hsa_circ_365721,RMVar_hsa_circ_32727,RMVar_hsa_circ_32897,RMVar_hsa_circ_3110,RMVar_hsa_circ_218708,RMVar_hsa_circ_218709,RMVar_hsa_circ_65007,RMVar_hsa_circ_304485 29735 RMVar_ID_29735 Human_SNP_ID_133314757 A-to-I Human chr3 - 52581346 52581345 52581346 ACCATCATGCCTGGCTAATTTTTGTATCTTTAATAGAGATGGGGTTTTACCATGTTGGCCAGTCT ACCATCATGCCTGGCTAATTTTTGTATCTTTA_TAGAGATGGGGTTTTACCATGTTGGCCAGTCT AT A PBRM1 Ensembl:ENSG00000163939 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1322210904 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_261,RMVar_hsa_circ_13769,RMVar_hsa_circ_31,RMVar_hsa_circ_341821,RMVar_hsa_circ_64282,RMVar_hsa_circ_39930,RMVar_hsa_circ_297405,RMVar_hsa_circ_342373,RMVar_hsa_circ_365721,RMVar_hsa_circ_32727,RMVar_hsa_circ_32897,RMVar_hsa_circ_3110,RMVar_hsa_circ_218708,RMVar_hsa_circ_218709,RMVar_hsa_circ_65007,RMVar_hsa_circ_304485 29736 RMVar_ID_29736 Human_SNP_ID_133314900 A-to-I Human chr3 - 52581775 52581775 52581775 AAATTAGCCAGGCGTGGTGGCACGTGCCTGTAATCTCAGCTTCTCGGGAGGTTGAGGCAGGAAAA AAATTAGCCAGGCGTGGTGGCACGTGCCTGTAGTCTCAGCTTCTCGGGAGGTTGAGGCAGGAAAA T C PBRM1 Ensembl:ENSG00000163939 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs906167432 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_261,RMVar_hsa_circ_13769,RMVar_hsa_circ_31,RMVar_hsa_circ_341821,RMVar_hsa_circ_64282,RMVar_hsa_circ_39930,RMVar_hsa_circ_297405,RMVar_hsa_circ_342373,RMVar_hsa_circ_365721,RMVar_hsa_circ_32727,RMVar_hsa_circ_32897,RMVar_hsa_circ_3110,RMVar_hsa_circ_218708,RMVar_hsa_circ_218709,RMVar_hsa_circ_65007,RMVar_hsa_circ_304485 29737 RMVar_ID_29737 Human_SNP_ID_133315143 A-to-I Human chr3 - 52582606 52582602 52582607 GCAGAATTATCCGGTCGGGTGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGA GCAGAATTATCCGGTCGGGTGCAGTGGCTCA_____GTAATCCCAGCACTTTGGGAGGCTGAGGA CAGGTG C PBRM1 Ensembl:ENSG00000163939 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1357708640 Functional Loss DEL dbSNP153 32..36 33 - - - RMVar_hsa_circ_261,RMVar_hsa_circ_13769,RMVar_hsa_circ_31,RMVar_hsa_circ_341821,RMVar_hsa_circ_64282,RMVar_hsa_circ_39930,RMVar_hsa_circ_297405,RMVar_hsa_circ_342373,RMVar_hsa_circ_365721,RMVar_hsa_circ_32727,RMVar_hsa_circ_32897,RMVar_hsa_circ_3110,RMVar_hsa_circ_218708,RMVar_hsa_circ_218709,RMVar_hsa_circ_65007,RMVar_hsa_circ_304485 29738 RMVar_ID_29738 Human_SNP_ID_133322664 A-to-I Human chr3 - 52611553 52611553 52611553 GTGATCTGCCCACCTTGGCCTCCCATAGTACTAGTATTGCAGGCATGAGCCACAGCTCCTGGCCC GTGATCTGCCCACCTTGGCCTCCCATAGTACTGGTATTGCAGGCATGAGCCACAGCTCCTGGCCC T C PBRM1 Ensembl:ENSG00000163939 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1259030119 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_261,RMVar_hsa_circ_31,RMVar_hsa_circ_341821,RMVar_hsa_circ_64282,RMVar_hsa_circ_39930,RMVar_hsa_circ_342373,RMVar_hsa_circ_32727,RMVar_hsa_circ_32897,RMVar_hsa_circ_356011,RMVar_hsa_circ_49638,RMVar_hsa_circ_46279,RMVar_hsa_circ_8654,RMVar_hsa_circ_13316,RMVar_hsa_circ_48371,RMVar_hsa_circ_102407,RMVar_hsa_circ_25637,RMVar_hsa_circ_9584,RMVar_hsa_circ_332610,RMVar_hsa_circ_218711,RMVar_hsa_circ_218712,RMVar_hsa_circ_360796,RMVar_hsa_circ_363974,RMVar_hsa_circ_352306,RMVar_hsa_circ_70551,RMVar_hsa_circ_321951,RMVar_hsa_circ_45061,RMVar_hsa_circ_218713,RMVar_hsa_circ_218714,RMVar_hsa_circ_218715,RMVar_hsa_circ_354633,RMVar_hsa_circ_315463 29739 RMVar_ID_29739 Human_SNP_ID_133322665 A-to-I Human chr3 - 52611553 52611553 52611553 GTGATCTGCCCACCTTGGCCTCCCATAGTACTAGTATTGCAGGCATGAGCCACAGCTCCTGGCCC GTGATCTGCCCACCTTGGCCTCCCATAGTACTCGTATTGCAGGCATGAGCCACAGCTCCTGGCCC T G PBRM1 Ensembl:ENSG00000163939 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1259030119 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_261,RMVar_hsa_circ_31,RMVar_hsa_circ_341821,RMVar_hsa_circ_64282,RMVar_hsa_circ_39930,RMVar_hsa_circ_342373,RMVar_hsa_circ_32727,RMVar_hsa_circ_32897,RMVar_hsa_circ_356011,RMVar_hsa_circ_49638,RMVar_hsa_circ_46279,RMVar_hsa_circ_8654,RMVar_hsa_circ_13316,RMVar_hsa_circ_48371,RMVar_hsa_circ_102407,RMVar_hsa_circ_25637,RMVar_hsa_circ_9584,RMVar_hsa_circ_332610,RMVar_hsa_circ_218711,RMVar_hsa_circ_218712,RMVar_hsa_circ_360796,RMVar_hsa_circ_363974,RMVar_hsa_circ_352306,RMVar_hsa_circ_70551,RMVar_hsa_circ_321951,RMVar_hsa_circ_45061,RMVar_hsa_circ_218713,RMVar_hsa_circ_218714,RMVar_hsa_circ_218715,RMVar_hsa_circ_354633,RMVar_hsa_circ_315463 29740 RMVar_ID_29740 Human_SNP_ID_133322679 A-to-I Human chr3 - 52611620 52611620 52611620 TTTTGTATTTTTAGTAGAGACAGGGTTTTGCTATGTTGCCAGGCTGGTCTTGAACTCCTGGGCTC TTTTGTATTTTTAGTAGAGACAGGGTTTTGCTGTGTTGCCAGGCTGGTCTTGAACTCCTGGGCTC T C PBRM1 Ensembl:ENSG00000163939 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1452365084 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5208125 RMVar_hsa_circ_261,RMVar_hsa_circ_31,RMVar_hsa_circ_341821,RMVar_hsa_circ_64282,RMVar_hsa_circ_39930,RMVar_hsa_circ_342373,RMVar_hsa_circ_32727,RMVar_hsa_circ_32897,RMVar_hsa_circ_356011,RMVar_hsa_circ_49638,RMVar_hsa_circ_46279,RMVar_hsa_circ_8654,RMVar_hsa_circ_13316,RMVar_hsa_circ_48371,RMVar_hsa_circ_102407,RMVar_hsa_circ_25637,RMVar_hsa_circ_9584,RMVar_hsa_circ_332610,RMVar_hsa_circ_218711,RMVar_hsa_circ_218712,RMVar_hsa_circ_360796,RMVar_hsa_circ_363974,RMVar_hsa_circ_352306,RMVar_hsa_circ_70551,RMVar_hsa_circ_321951,RMVar_hsa_circ_45061,RMVar_hsa_circ_218713,RMVar_hsa_circ_218714,RMVar_hsa_circ_218715,RMVar_hsa_circ_354633,RMVar_hsa_circ_315463 29741 RMVar_ID_29741 Human_SNP_ID_133322991 A-to-I Human chr3 - 52612653 52612653 52612653 GTGATCCGTCCGCCTCCGCCTCCCAAAGTGCTAGGATTACAGGCATGAGCCACCGCACCCAGCAG GTGATCCGTCCGCCTCCGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCACCCAGCAG T C PBRM1 Ensembl:ENSG00000163939 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1262207902 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14892365 RMVar_hsa_circ_261,RMVar_hsa_circ_31,RMVar_hsa_circ_341821,RMVar_hsa_circ_64282,RMVar_hsa_circ_39930,RMVar_hsa_circ_342373,RMVar_hsa_circ_32727,RMVar_hsa_circ_32897,RMVar_hsa_circ_356011,RMVar_hsa_circ_49638,RMVar_hsa_circ_46279,RMVar_hsa_circ_8654,RMVar_hsa_circ_13316,RMVar_hsa_circ_48371,RMVar_hsa_circ_102407,RMVar_hsa_circ_25637,RMVar_hsa_circ_9584,RMVar_hsa_circ_332610,RMVar_hsa_circ_218711,RMVar_hsa_circ_218712,RMVar_hsa_circ_360796,RMVar_hsa_circ_363974,RMVar_hsa_circ_352306,RMVar_hsa_circ_70551,RMVar_hsa_circ_321951,RMVar_hsa_circ_45061,RMVar_hsa_circ_218713,RMVar_hsa_circ_218714,RMVar_hsa_circ_218715,RMVar_hsa_circ_354633,RMVar_hsa_circ_315463 29742 RMVar_ID_29742 Human_SNP_ID_133323042 A-to-I Human chr3 - 52612846 52612846 52612846 GCTGGAGTGCAGTGGCACGATCTCGGCTCACTACAGACTCCGTCTCCTGGGTTCCCCCAATTCTT GCTGGAGTGCAGTGGCACGATCTCGGCTCACTGCAGACTCCGTCTCCTGGGTTCCCCCAATTCTT T C PBRM1 Ensembl:ENSG00000163939 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs990016308 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7210064,Human_RBP_ID_14892370 RMVar_hsa_circ_261,RMVar_hsa_circ_31,RMVar_hsa_circ_341821,RMVar_hsa_circ_64282,RMVar_hsa_circ_39930,RMVar_hsa_circ_342373,RMVar_hsa_circ_32727,RMVar_hsa_circ_32897,RMVar_hsa_circ_356011,RMVar_hsa_circ_49638,RMVar_hsa_circ_46279,RMVar_hsa_circ_8654,RMVar_hsa_circ_13316,RMVar_hsa_circ_48371,RMVar_hsa_circ_102407,RMVar_hsa_circ_25637,RMVar_hsa_circ_9584,RMVar_hsa_circ_332610,RMVar_hsa_circ_218711,RMVar_hsa_circ_218712,RMVar_hsa_circ_360796,RMVar_hsa_circ_363974,RMVar_hsa_circ_352306,RMVar_hsa_circ_70551,RMVar_hsa_circ_321951,RMVar_hsa_circ_45061,RMVar_hsa_circ_218713,RMVar_hsa_circ_218714,RMVar_hsa_circ_218715,RMVar_hsa_circ_354633,RMVar_hsa_circ_315463 29743 RMVar_ID_29743 Human_SNP_ID_133323342 A-to-I Human chr3 - 52614211 52614211 52614211 GCCACCAGGCCCAGCCAGTTTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGC GCCACCAGGCCCAGCCAGTTTTTTGTATTTTTGGTAGAGATGGGGTTTCACCATGTTGGCCAGGC T C PBRM1 Ensembl:ENSG00000163939 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1030740697 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_261,RMVar_hsa_circ_31,RMVar_hsa_circ_341821,RMVar_hsa_circ_64282,RMVar_hsa_circ_39930,RMVar_hsa_circ_342373,RMVar_hsa_circ_32727,RMVar_hsa_circ_32897,RMVar_hsa_circ_356011,RMVar_hsa_circ_49638,RMVar_hsa_circ_46279,RMVar_hsa_circ_8654,RMVar_hsa_circ_13316,RMVar_hsa_circ_48371,RMVar_hsa_circ_102407,RMVar_hsa_circ_25637,RMVar_hsa_circ_9584,RMVar_hsa_circ_332610,RMVar_hsa_circ_218711,RMVar_hsa_circ_218712,RMVar_hsa_circ_360796,RMVar_hsa_circ_363974,RMVar_hsa_circ_352306,RMVar_hsa_circ_70551,RMVar_hsa_circ_321951,RMVar_hsa_circ_45061,RMVar_hsa_circ_218713,RMVar_hsa_circ_218714,RMVar_hsa_circ_218715,RMVar_hsa_circ_354633,RMVar_hsa_circ_315463 29744 RMVar_ID_29744 Human_SNP_ID_133328712 A-to-I Human chr3 - 52636633 52636633 52636633 CCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGTCACCTGCCACCACACCCGGCTAATTTTTTT CCTGCCTCAGCCTCCCGAGTAGCTGGGATTACGGTCACCTGCCACCACACCCGGCTAATTTTTTT T C PBRM1 Ensembl:ENSG00000163939 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1357995410 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_261,RMVar_hsa_circ_31,RMVar_hsa_circ_39930,RMVar_hsa_circ_32897,RMVar_hsa_circ_9644,RMVar_hsa_circ_356011,RMVar_hsa_circ_8654,RMVar_hsa_circ_13316,RMVar_hsa_circ_48371,RMVar_hsa_circ_25637,RMVar_hsa_circ_9584,RMVar_hsa_circ_218712,RMVar_hsa_circ_360796,RMVar_hsa_circ_363974,RMVar_hsa_circ_352306,RMVar_hsa_circ_70551,RMVar_hsa_circ_45061,RMVar_hsa_circ_319417,RMVar_hsa_circ_65900,RMVar_hsa_circ_302530,RMVar_hsa_circ_48263,RMVar_hsa_circ_49178,RMVar_hsa_circ_14162,RMVar_hsa_circ_44799,RMVar_hsa_circ_48261,RMVar_hsa_circ_74144,RMVar_hsa_circ_307662,RMVar_hsa_circ_218718,RMVar_hsa_circ_111221,RMVar_hsa_circ_56763,RMVar_hsa_circ_218720,RMVar_hsa_circ_34280,RMVar_hsa_circ_218719,RMVar_hsa_circ_365683,RMVar_hsa_circ_348458,RMVar_hsa_circ_357964,RMVar_hsa_circ_299690,RMVar_hsa_circ_340665,RMVar_hsa_circ_218722,RMVar_hsa_circ_218723,RMVar_hsa_circ_361151,RMVar_hsa_circ_364312,RMVar_hsa_circ_367693,RMVar_hsa_circ_360476,RMVar_hsa_circ_299283,RMVar_hsa_circ_48116,RMVar_hsa_circ_218724,RMVar_hsa_circ_218726,RMVar_hsa_circ_218727,RMVar_hsa_circ_218725 29745 RMVar_ID_29745 Human_SNP_ID_133329407 A-to-I Human chr3 - 52638732 52638732 52638732 AATTAGCCGGGCGTGGTGTGGTGCATGTCTGTAGTCCTACCTACTTGGTAGGCTAAGGCAGGAGG AATTAGCCGGGCGTGGTGTGGTGCATGTCTGTGGTCCTACCTACTTGGTAGGCTAAGGCAGGAGG T C PBRM1 Ensembl:ENSG00000163939 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1415704830 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_261,RMVar_hsa_circ_31,RMVar_hsa_circ_39930,RMVar_hsa_circ_32897,RMVar_hsa_circ_9644,RMVar_hsa_circ_356011,RMVar_hsa_circ_8654,RMVar_hsa_circ_13316,RMVar_hsa_circ_48371,RMVar_hsa_circ_25637,RMVar_hsa_circ_9584,RMVar_hsa_circ_218712,RMVar_hsa_circ_360796,RMVar_hsa_circ_363974,RMVar_hsa_circ_352306,RMVar_hsa_circ_70551,RMVar_hsa_circ_45061,RMVar_hsa_circ_319417,RMVar_hsa_circ_65900,RMVar_hsa_circ_302530,RMVar_hsa_circ_48263,RMVar_hsa_circ_49178,RMVar_hsa_circ_14162,RMVar_hsa_circ_44799,RMVar_hsa_circ_48261,RMVar_hsa_circ_74144,RMVar_hsa_circ_307662,RMVar_hsa_circ_218718,RMVar_hsa_circ_111221,RMVar_hsa_circ_56763,RMVar_hsa_circ_218720,RMVar_hsa_circ_34280,RMVar_hsa_circ_218719,RMVar_hsa_circ_365683,RMVar_hsa_circ_348458,RMVar_hsa_circ_357964,RMVar_hsa_circ_299690,RMVar_hsa_circ_340665,RMVar_hsa_circ_218722,RMVar_hsa_circ_218723,RMVar_hsa_circ_361151,RMVar_hsa_circ_364312,RMVar_hsa_circ_367693,RMVar_hsa_circ_360476,RMVar_hsa_circ_299283,RMVar_hsa_circ_48116,RMVar_hsa_circ_218724,RMVar_hsa_circ_218726,RMVar_hsa_circ_218727,RMVar_hsa_circ_218725 29746 RMVar_ID_29746 Human_SNP_ID_133329705 A-to-I Human chr3 - 52639651 52639651 52639651 CTTGGCTCCCTACAACCTCCACTCCTGGGCTCAAGCAGTCCTCCCACCTCAGCCTCCCTAGTAGC CTTGGCTCCCTACAACCTCCACTCCTGGGCTCGAGCAGTCCTCCCACCTCAGCCTCCCTAGTAGC T C PBRM1 Ensembl:ENSG00000163939 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs960511538 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_261,RMVar_hsa_circ_31,RMVar_hsa_circ_39930,RMVar_hsa_circ_32897,RMVar_hsa_circ_9644,RMVar_hsa_circ_356011,RMVar_hsa_circ_8654,RMVar_hsa_circ_13316,RMVar_hsa_circ_48371,RMVar_hsa_circ_25637,RMVar_hsa_circ_9584,RMVar_hsa_circ_218712,RMVar_hsa_circ_360796,RMVar_hsa_circ_363974,RMVar_hsa_circ_352306,RMVar_hsa_circ_70551,RMVar_hsa_circ_45061,RMVar_hsa_circ_319417,RMVar_hsa_circ_65900,RMVar_hsa_circ_302530,RMVar_hsa_circ_48263,RMVar_hsa_circ_49178,RMVar_hsa_circ_14162,RMVar_hsa_circ_44799,RMVar_hsa_circ_48261,RMVar_hsa_circ_74144,RMVar_hsa_circ_307662,RMVar_hsa_circ_218718,RMVar_hsa_circ_111221,RMVar_hsa_circ_56763,RMVar_hsa_circ_218720,RMVar_hsa_circ_34280,RMVar_hsa_circ_218719,RMVar_hsa_circ_365683,RMVar_hsa_circ_348458,RMVar_hsa_circ_357964,RMVar_hsa_circ_299690,RMVar_hsa_circ_340665,RMVar_hsa_circ_218722,RMVar_hsa_circ_218723,RMVar_hsa_circ_361151,RMVar_hsa_circ_364312,RMVar_hsa_circ_367693,RMVar_hsa_circ_360476,RMVar_hsa_circ_299283,RMVar_hsa_circ_48116,RMVar_hsa_circ_218724,RMVar_hsa_circ_218726,RMVar_hsa_circ_218727,RMVar_hsa_circ_218725 29747 RMVar_ID_29747 Human_SNP_ID_133329958 A-to-I Human chr3 - 52640715 52640715 52640715 ATCACTTGAACCGAGGAAGTGGAGACTGCAGTAAACCGAGATCACACCACTGTACTCCAGCCTGG ATCACTTGAACCGAGGAAGTGGAGACTGCAGTGAACCGAGATCACACCACTGTACTCCAGCCTGG T C PBRM1 Ensembl:ENSG00000163939 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs560386950 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14892640 RMVar_hsa_circ_261,RMVar_hsa_circ_31,RMVar_hsa_circ_39930,RMVar_hsa_circ_32897,RMVar_hsa_circ_9644,RMVar_hsa_circ_356011,RMVar_hsa_circ_8654,RMVar_hsa_circ_13316,RMVar_hsa_circ_48371,RMVar_hsa_circ_25637,RMVar_hsa_circ_9584,RMVar_hsa_circ_218712,RMVar_hsa_circ_360796,RMVar_hsa_circ_363974,RMVar_hsa_circ_352306,RMVar_hsa_circ_70551,RMVar_hsa_circ_45061,RMVar_hsa_circ_319417,RMVar_hsa_circ_65900,RMVar_hsa_circ_302530,RMVar_hsa_circ_48263,RMVar_hsa_circ_49178,RMVar_hsa_circ_14162,RMVar_hsa_circ_44799,RMVar_hsa_circ_48261,RMVar_hsa_circ_74144,RMVar_hsa_circ_307662,RMVar_hsa_circ_218718,RMVar_hsa_circ_111221,RMVar_hsa_circ_56763,RMVar_hsa_circ_218720,RMVar_hsa_circ_34280,RMVar_hsa_circ_218719,RMVar_hsa_circ_365683,RMVar_hsa_circ_348458,RMVar_hsa_circ_357964,RMVar_hsa_circ_299690,RMVar_hsa_circ_340665,RMVar_hsa_circ_218722,RMVar_hsa_circ_218723,RMVar_hsa_circ_361151,RMVar_hsa_circ_364312,RMVar_hsa_circ_367693,RMVar_hsa_circ_360476,RMVar_hsa_circ_299283,RMVar_hsa_circ_48116,RMVar_hsa_circ_218724,RMVar_hsa_circ_218726,RMVar_hsa_circ_218727,RMVar_hsa_circ_218725 29748 RMVar_ID_29748 Human_SNP_ID_133329977 A-to-I Human chr3 - 52640794 52640794 52640794 TCTCTACTAAAAATACAAAAAATTGGCCAGGTATGGTGGAGCGCACCTGTAGTCTCAGCTACTCG TCTCTACTAAAAATACAAAAAATTGGCCAGGTGTGGTGGAGCGCACCTGTAGTCTCAGCTACTCG T C PBRM1 Ensembl:ENSG00000163939 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1320640400 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_261,RMVar_hsa_circ_31,RMVar_hsa_circ_39930,RMVar_hsa_circ_32897,RMVar_hsa_circ_9644,RMVar_hsa_circ_356011,RMVar_hsa_circ_8654,RMVar_hsa_circ_13316,RMVar_hsa_circ_48371,RMVar_hsa_circ_25637,RMVar_hsa_circ_9584,RMVar_hsa_circ_218712,RMVar_hsa_circ_360796,RMVar_hsa_circ_363974,RMVar_hsa_circ_352306,RMVar_hsa_circ_70551,RMVar_hsa_circ_45061,RMVar_hsa_circ_319417,RMVar_hsa_circ_65900,RMVar_hsa_circ_302530,RMVar_hsa_circ_48263,RMVar_hsa_circ_49178,RMVar_hsa_circ_14162,RMVar_hsa_circ_44799,RMVar_hsa_circ_48261,RMVar_hsa_circ_74144,RMVar_hsa_circ_307662,RMVar_hsa_circ_218718,RMVar_hsa_circ_111221,RMVar_hsa_circ_56763,RMVar_hsa_circ_218720,RMVar_hsa_circ_34280,RMVar_hsa_circ_218719,RMVar_hsa_circ_365683,RMVar_hsa_circ_348458,RMVar_hsa_circ_357964,RMVar_hsa_circ_299690,RMVar_hsa_circ_340665,RMVar_hsa_circ_218722,RMVar_hsa_circ_218723,RMVar_hsa_circ_361151,RMVar_hsa_circ_364312,RMVar_hsa_circ_367693,RMVar_hsa_circ_360476,RMVar_hsa_circ_299283,RMVar_hsa_circ_48116,RMVar_hsa_circ_218724,RMVar_hsa_circ_218726,RMVar_hsa_circ_218727,RMVar_hsa_circ_218725 29749 RMVar_ID_29749 Human_SNP_ID_133329991 A-to-I Human chr3 - 52640840 52640840 52640840 GAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCGTGTCTCTACTAAAAATACAAA GAGGTCAGGAGTTCAAGACCAGCCTGGCCAACCTGGTGAAACCGTGTCTCTACTAAAAATACAAA T G PBRM1 Ensembl:ENSG00000163939 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs192123821 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_261,RMVar_hsa_circ_31,RMVar_hsa_circ_39930,RMVar_hsa_circ_32897,RMVar_hsa_circ_9644,RMVar_hsa_circ_356011,RMVar_hsa_circ_8654,RMVar_hsa_circ_13316,RMVar_hsa_circ_48371,RMVar_hsa_circ_25637,RMVar_hsa_circ_9584,RMVar_hsa_circ_218712,RMVar_hsa_circ_360796,RMVar_hsa_circ_363974,RMVar_hsa_circ_352306,RMVar_hsa_circ_70551,RMVar_hsa_circ_45061,RMVar_hsa_circ_319417,RMVar_hsa_circ_65900,RMVar_hsa_circ_302530,RMVar_hsa_circ_48263,RMVar_hsa_circ_49178,RMVar_hsa_circ_14162,RMVar_hsa_circ_44799,RMVar_hsa_circ_48261,RMVar_hsa_circ_74144,RMVar_hsa_circ_307662,RMVar_hsa_circ_218718,RMVar_hsa_circ_111221,RMVar_hsa_circ_56763,RMVar_hsa_circ_218720,RMVar_hsa_circ_34280,RMVar_hsa_circ_218719,RMVar_hsa_circ_365683,RMVar_hsa_circ_348458,RMVar_hsa_circ_357964,RMVar_hsa_circ_299690,RMVar_hsa_circ_340665,RMVar_hsa_circ_218722,RMVar_hsa_circ_218723,RMVar_hsa_circ_361151,RMVar_hsa_circ_364312,RMVar_hsa_circ_367693,RMVar_hsa_circ_360476,RMVar_hsa_circ_299283,RMVar_hsa_circ_48116,RMVar_hsa_circ_218724,RMVar_hsa_circ_218726,RMVar_hsa_circ_218727,RMVar_hsa_circ_218725 29750 RMVar_ID_29750 Human_SNP_ID_133330585 A-to-I Human chr3 - 52642924 52642924 52642924 AAATTAGCTGGGTGTGGTGGCGGGTGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAA AAATTAGCTGGGTGTGGTGGCGGGTGCCTGTACTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAA T G PBRM1 Ensembl:ENSG00000163939 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs542628898 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_261,RMVar_hsa_circ_31,RMVar_hsa_circ_39930,RMVar_hsa_circ_32897,RMVar_hsa_circ_9644,RMVar_hsa_circ_356011,RMVar_hsa_circ_8654,RMVar_hsa_circ_13316,RMVar_hsa_circ_48371,RMVar_hsa_circ_25637,RMVar_hsa_circ_9584,RMVar_hsa_circ_218712,RMVar_hsa_circ_360796,RMVar_hsa_circ_363974,RMVar_hsa_circ_352306,RMVar_hsa_circ_70551,RMVar_hsa_circ_45061,RMVar_hsa_circ_65900,RMVar_hsa_circ_302530,RMVar_hsa_circ_48263,RMVar_hsa_circ_49178,RMVar_hsa_circ_14162,RMVar_hsa_circ_48261,RMVar_hsa_circ_74144,RMVar_hsa_circ_307662,RMVar_hsa_circ_218718,RMVar_hsa_circ_111221,RMVar_hsa_circ_56763,RMVar_hsa_circ_218720,RMVar_hsa_circ_34280,RMVar_hsa_circ_218719,RMVar_hsa_circ_365683,RMVar_hsa_circ_348458,RMVar_hsa_circ_357964,RMVar_hsa_circ_299690,RMVar_hsa_circ_340665,RMVar_hsa_circ_218722,RMVar_hsa_circ_218723,RMVar_hsa_circ_364312,RMVar_hsa_circ_367693,RMVar_hsa_circ_360476,RMVar_hsa_circ_299283,RMVar_hsa_circ_48116,RMVar_hsa_circ_218728,RMVar_hsa_circ_218736,RMVar_hsa_circ_304982,RMVar_hsa_circ_328548,RMVar_hsa_circ_218724,RMVar_hsa_circ_218726,RMVar_hsa_circ_218727,RMVar_hsa_circ_218725,RMVar_hsa_circ_364481,RMVar_hsa_circ_376564,RMVar_hsa_circ_334401,RMVar_hsa_circ_312283,RMVar_hsa_circ_322246,RMVar_hsa_circ_309126,RMVar_hsa_circ_298282,RMVar_hsa_circ_303717,RMVar_hsa_circ_277774,RMVar_hsa_circ_218732,RMVar_hsa_circ_218734,RMVar_hsa_circ_218735,RMVar_hsa_circ_218733,RMVar_hsa_circ_218730,RMVar_hsa_circ_218731,RMVar_hsa_circ_218729 29751 RMVar_ID_29751 Human_SNP_ID_133330855 A-to-I Human chr3 - 52643885 52643885 52643885 CCACTGCAACCTCCACCTCCCAGGTTCAAGCAATTCTTTTGCCTTAGCCTCCCAAGTAGCTGGGA CCACTGCAACCTCCACCTCCCAGGTTCAAGCAGTTCTTTTGCCTTAGCCTCCCAAGTAGCTGGGA T C PBRM1 Ensembl:ENSG00000163939 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs746294338 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_261,RMVar_hsa_circ_31,RMVar_hsa_circ_39930,RMVar_hsa_circ_32897,RMVar_hsa_circ_9644,RMVar_hsa_circ_356011,RMVar_hsa_circ_8654,RMVar_hsa_circ_13316,RMVar_hsa_circ_48371,RMVar_hsa_circ_25637,RMVar_hsa_circ_9584,RMVar_hsa_circ_218712,RMVar_hsa_circ_360796,RMVar_hsa_circ_363974,RMVar_hsa_circ_352306,RMVar_hsa_circ_70551,RMVar_hsa_circ_45061,RMVar_hsa_circ_302530,RMVar_hsa_circ_48263,RMVar_hsa_circ_14162,RMVar_hsa_circ_48261,RMVar_hsa_circ_74144,RMVar_hsa_circ_307662,RMVar_hsa_circ_111221,RMVar_hsa_circ_56763,RMVar_hsa_circ_218720,RMVar_hsa_circ_34280,RMVar_hsa_circ_218719,RMVar_hsa_circ_365683,RMVar_hsa_circ_357964,RMVar_hsa_circ_299690,RMVar_hsa_circ_340665,RMVar_hsa_circ_218723,RMVar_hsa_circ_364312,RMVar_hsa_circ_360476,RMVar_hsa_circ_299283,RMVar_hsa_circ_48116,RMVar_hsa_circ_218728,RMVar_hsa_circ_304982,RMVar_hsa_circ_328548,RMVar_hsa_circ_218724,RMVar_hsa_circ_218726,RMVar_hsa_circ_218725,RMVar_hsa_circ_364481,RMVar_hsa_circ_376564,RMVar_hsa_circ_334401,RMVar_hsa_circ_312283,RMVar_hsa_circ_322246,RMVar_hsa_circ_309126,RMVar_hsa_circ_298282,RMVar_hsa_circ_277774,RMVar_hsa_circ_218732,RMVar_hsa_circ_218734,RMVar_hsa_circ_218735,RMVar_hsa_circ_218733,RMVar_hsa_circ_218730,RMVar_hsa_circ_218731,RMVar_hsa_circ_218729,RMVar_hsa_circ_218741,RMVar_hsa_circ_280802,RMVar_hsa_circ_304666,RMVar_hsa_circ_338233,RMVar_hsa_circ_324723,RMVar_hsa_circ_291091,RMVar_hsa_circ_218742,RMVar_hsa_circ_218739,RMVar_hsa_circ_218740,RMVar_hsa_circ_218738 29752 RMVar_ID_29752 Human_SNP_ID_133330866 A-to-I Human chr3 - 52643925 52643925 52643925 CTCTGTTGCCCAAACTGGATTGCAGTGGCACAATCTCGGCCCACTGCAACCTCCACCTCCCAGGT CTCTGTTGCCCAAACTGGATTGCAGTGGCACAGTCTCGGCCCACTGCAACCTCCACCTCCCAGGT T C PBRM1 Ensembl:ENSG00000163939 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1012782592 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_261,RMVar_hsa_circ_31,RMVar_hsa_circ_39930,RMVar_hsa_circ_32897,RMVar_hsa_circ_9644,RMVar_hsa_circ_356011,RMVar_hsa_circ_8654,RMVar_hsa_circ_13316,RMVar_hsa_circ_48371,RMVar_hsa_circ_25637,RMVar_hsa_circ_9584,RMVar_hsa_circ_218712,RMVar_hsa_circ_360796,RMVar_hsa_circ_363974,RMVar_hsa_circ_352306,RMVar_hsa_circ_70551,RMVar_hsa_circ_45061,RMVar_hsa_circ_302530,RMVar_hsa_circ_48263,RMVar_hsa_circ_14162,RMVar_hsa_circ_48261,RMVar_hsa_circ_74144,RMVar_hsa_circ_307662,RMVar_hsa_circ_111221,RMVar_hsa_circ_56763,RMVar_hsa_circ_218720,RMVar_hsa_circ_34280,RMVar_hsa_circ_218719,RMVar_hsa_circ_365683,RMVar_hsa_circ_357964,RMVar_hsa_circ_299690,RMVar_hsa_circ_340665,RMVar_hsa_circ_218723,RMVar_hsa_circ_364312,RMVar_hsa_circ_360476,RMVar_hsa_circ_299283,RMVar_hsa_circ_48116,RMVar_hsa_circ_218728,RMVar_hsa_circ_304982,RMVar_hsa_circ_328548,RMVar_hsa_circ_218724,RMVar_hsa_circ_218726,RMVar_hsa_circ_218725,RMVar_hsa_circ_364481,RMVar_hsa_circ_376564,RMVar_hsa_circ_334401,RMVar_hsa_circ_312283,RMVar_hsa_circ_322246,RMVar_hsa_circ_309126,RMVar_hsa_circ_298282,RMVar_hsa_circ_277774,RMVar_hsa_circ_218732,RMVar_hsa_circ_218734,RMVar_hsa_circ_218735,RMVar_hsa_circ_218733,RMVar_hsa_circ_218730,RMVar_hsa_circ_218731,RMVar_hsa_circ_218729,RMVar_hsa_circ_218741,RMVar_hsa_circ_280802,RMVar_hsa_circ_304666,RMVar_hsa_circ_338233,RMVar_hsa_circ_324723,RMVar_hsa_circ_291091,RMVar_hsa_circ_218742,RMVar_hsa_circ_218739,RMVar_hsa_circ_218740,RMVar_hsa_circ_218738 29753 RMVar_ID_29753 Human_SNP_ID_133333708 A-to-I Human chr3 - 52654871 52654871 52654871 AGTTTGGAGGATCACTTGAGCCTAGGAGTTCAAGGCCGCAGTGAGCTGTGATCATGCCACTTCAC AGTTTGGAGGATCACTTGAGCCTAGGAGTTCAGGGCCGCAGTGAGCTGTGATCATGCCACTTCAC T C PBRM1 Ensembl:ENSG00000163939 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs952703834 Functional Loss SNV dbSNP153 33..33 33 - - - 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_70551,RMVar_hsa_circ_45061,RMVar_hsa_circ_48263,RMVar_hsa_circ_14249,RMVar_hsa_circ_48261,RMVar_hsa_circ_111221,RMVar_hsa_circ_56763,RMVar_hsa_circ_218720,RMVar_hsa_circ_34280,RMVar_hsa_circ_299690,RMVar_hsa_circ_218723,RMVar_hsa_circ_364312,RMVar_hsa_circ_360476,RMVar_hsa_circ_48116,RMVar_hsa_circ_218728,RMVar_hsa_circ_304982,RMVar_hsa_circ_218724,RMVar_hsa_circ_218725,RMVar_hsa_circ_364481,RMVar_hsa_circ_376564,RMVar_hsa_circ_334401,RMVar_hsa_circ_312283,RMVar_hsa_circ_322246,RMVar_hsa_circ_309126,RMVar_hsa_circ_218732,RMVar_hsa_circ_218730,RMVar_hsa_circ_218731,RMVar_hsa_circ_218729,RMVar_hsa_circ_218741,RMVar_hsa_circ_280802,RMVar_hsa_circ_324723,RMVar_hsa_circ_291091,RMVar_hsa_circ_218742,RMVar_hsa_circ_218740,RMVar_hsa_circ_35685,RMVar_hsa_circ_301106,RMVar_hsa_circ_39948,RMVar_hsa_circ_33167,RMVar_hsa_circ_218752,RMVar_hsa_circ_120215,RMVar_hsa_circ_332668,RMVar_hsa_circ_349510,RMVar_hsa_circ_218743,RMVar_hsa_circ_339011,RMVar_hsa_circ_318672,RMVar_hsa_circ_322737,RMVar_hsa_circ_218748,RMVar_hsa_circ_218750,RMVar_hsa_circ_218751,RMVar_hsa_circ_218749,RMVar_hsa_circ_7524,RMVar_hsa_circ_293106,RMVar_hsa_circ_298720,RMVar_hsa_circ_9647,RMVar_hsa_circ_218753,RMVar_hsa_circ_218754 29754 RMVar_ID_29754 Human_SNP_ID_133333709 A-to-I Human chr3 - 52654880 52654880 52654880 GTGGGGCTGAGTTTGGAGGATCACTTGAGCCTAGGAGTTCAAGGCCGCAGTGAGCTGTGATCATG GTGGGGCTGAGTTTGGAGGATCACTTGAGCCTGGGAGTTCAAGGCCGCAGTGAGCTGTGATCATG T C PBRM1 Ensembl:ENSG00000163939 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs374368706 Functional Loss SNV dbSNP153 33..33 33 - - - 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_70551,RMVar_hsa_circ_45061,RMVar_hsa_circ_48263,RMVar_hsa_circ_14249,RMVar_hsa_circ_48261,RMVar_hsa_circ_111221,RMVar_hsa_circ_56763,RMVar_hsa_circ_218720,RMVar_hsa_circ_34280,RMVar_hsa_circ_299690,RMVar_hsa_circ_218723,RMVar_hsa_circ_364312,RMVar_hsa_circ_360476,RMVar_hsa_circ_48116,RMVar_hsa_circ_218728,RMVar_hsa_circ_304982,RMVar_hsa_circ_218724,RMVar_hsa_circ_218725,RMVar_hsa_circ_364481,RMVar_hsa_circ_376564,RMVar_hsa_circ_334401,RMVar_hsa_circ_312283,RMVar_hsa_circ_322246,RMVar_hsa_circ_309126,RMVar_hsa_circ_218732,RMVar_hsa_circ_218730,RMVar_hsa_circ_218731,RMVar_hsa_circ_218729,RMVar_hsa_circ_218741,RMVar_hsa_circ_280802,RMVar_hsa_circ_324723,RMVar_hsa_circ_291091,RMVar_hsa_circ_218742,RMVar_hsa_circ_218740,RMVar_hsa_circ_35685,RMVar_hsa_circ_301106,RMVar_hsa_circ_39948,RMVar_hsa_circ_33167,RMVar_hsa_circ_218752,RMVar_hsa_circ_120215,RMVar_hsa_circ_332668,RMVar_hsa_circ_349510,RMVar_hsa_circ_218743,RMVar_hsa_circ_339011,RMVar_hsa_circ_318672,RMVar_hsa_circ_322737,RMVar_hsa_circ_218748,RMVar_hsa_circ_218750,RMVar_hsa_circ_218751,RMVar_hsa_circ_218749,RMVar_hsa_circ_7524,RMVar_hsa_circ_293106,RMVar_hsa_circ_298720,RMVar_hsa_circ_9647,RMVar_hsa_circ_218753,RMVar_hsa_circ_218754 29755 RMVar_ID_29755 Human_SNP_ID_133334200 A-to-I Human chr3 - 52657192 52657192 52657192 ACCATCACCACTATCTGGAACTTTTTAGTCTTACAAAACCAAAACTCCATACCCATTAAACACCA ACCATCACCACTATCTGGAACTTTTTAGTCTTTCAAAACCAAAACTCCATACCCATTAAACACCA T A PBRM1 Ensembl:ENSG00000163939 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs958349414 Functional Loss SNV dbSNP153 33..33 33 - - - 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_70551,RMVar_hsa_circ_45061,RMVar_hsa_circ_48263,RMVar_hsa_circ_14249,RMVar_hsa_circ_48261,RMVar_hsa_circ_111221,RMVar_hsa_circ_56763,RMVar_hsa_circ_218720,RMVar_hsa_circ_34280,RMVar_hsa_circ_299690,RMVar_hsa_circ_218723,RMVar_hsa_circ_364312,RMVar_hsa_circ_360476,RMVar_hsa_circ_48116,RMVar_hsa_circ_218728,RMVar_hsa_circ_304982,RMVar_hsa_circ_218724,RMVar_hsa_circ_218725,RMVar_hsa_circ_364481,RMVar_hsa_circ_376564,RMVar_hsa_circ_334401,RMVar_hsa_circ_312283,RMVar_hsa_circ_322246,RMVar_hsa_circ_309126,RMVar_hsa_circ_218732,RMVar_hsa_circ_218730,RMVar_hsa_circ_218731,RMVar_hsa_circ_218729,RMVar_hsa_circ_218741,RMVar_hsa_circ_280802,RMVar_hsa_circ_324723,RMVar_hsa_circ_291091,RMVar_hsa_circ_218742,RMVar_hsa_circ_218740,RMVar_hsa_circ_35685,RMVar_hsa_circ_301106,RMVar_hsa_circ_39948,RMVar_hsa_circ_33167,RMVar_hsa_circ_218752,RMVar_hsa_circ_120215,RMVar_hsa_circ_332668,RMVar_hsa_circ_349510,RMVar_hsa_circ_218743,RMVar_hsa_circ_339011,RMVar_hsa_circ_318672,RMVar_hsa_circ_322737,RMVar_hsa_circ_218748,RMVar_hsa_circ_218750,RMVar_hsa_circ_218751,RMVar_hsa_circ_218749,RMVar_hsa_circ_7524,RMVar_hsa_circ_293106,RMVar_hsa_circ_298720,RMVar_hsa_circ_9647,RMVar_hsa_circ_218753,RMVar_hsa_circ_218754 29756 RMVar_ID_29756 Human_SNP_ID_133343134 A-to-I Human chr3 + 52689805 52689805 52689805 CGAAACCCCATCTCTACTAAAATACAAATATTAGCCGGGCATGATGATGGGCACTTGTAGTCCCA CGAAACCCCATCTCTACTAAAATACAAATATTGGCCGGGCATGATGATGGGCACTTGTAGTCCCA A G GNL3 Ensembl:ENSG00000163938 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs888261345 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22726139 RMVar_hsa_circ_8685,RMVar_hsa_circ_124111,RMVar_hsa_circ_71418,RMVar_hsa_circ_63351,RMVar_hsa_circ_17945,RMVar_hsa_circ_348884,RMVar_hsa_circ_218769,RMVar_hsa_circ_363275,RMVar_hsa_circ_307136,RMVar_hsa_circ_61085,RMVar_hsa_circ_218770,RMVar_hsa_circ_371874,RMVar_hsa_circ_218772 29757 RMVar_ID_29757 Human_SNP_ID_133343145 A-to-I Human chr3 + 52689837 52689837 52689837 AGCCGGGCATGATGATGGGCACTTGTAGTCCCAGCTACTCGGAAGGCTGAGGCAGGAGAATTGCT AGCCGGGCATGATGATGGGCACTTGTAGTCCCGGCTACTCGGAAGGCTGAGGCAGGAGAATTGCT A G GNL3 Ensembl:ENSG00000163938 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs191411404 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22726139 RMVar_hsa_circ_8685,RMVar_hsa_circ_124111,RMVar_hsa_circ_71418,RMVar_hsa_circ_63351,RMVar_hsa_circ_17945,RMVar_hsa_circ_348884,RMVar_hsa_circ_218769,RMVar_hsa_circ_363275,RMVar_hsa_circ_307136,RMVar_hsa_circ_61085,RMVar_hsa_circ_218770,RMVar_hsa_circ_371874,RMVar_hsa_circ_218772 29758 RMVar_ID_29758 Human_SNP_ID_133343276 A-to-I Human chr3 + 52690439 52690439 52690439 TGCCCACCACCACGCCCAGCTAATTTTTTTGTATTTTTAGTAGAGACGGGGTTTTATCGTGTTAG TGCCCACCACCACGCCCAGCTAATTTTTTTGTGTTTTTAGTAGAGACGGGGTTTTATCGTGTTAG A G GNL3 Ensembl:ENSG00000163938 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs140272786 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8685,RMVar_hsa_circ_124111,RMVar_hsa_circ_71418,RMVar_hsa_circ_63351,RMVar_hsa_circ_17945,RMVar_hsa_circ_348884,RMVar_hsa_circ_218769,RMVar_hsa_circ_363275,RMVar_hsa_circ_307136,RMVar_hsa_circ_61085,RMVar_hsa_circ_218770,RMVar_hsa_circ_371874,RMVar_hsa_circ_218772 29759 RMVar_ID_29759 Human_SNP_ID_133346882 A-to-I Human chr3 - 52702464 52702462 52702464 ATGGCTTACTGCAGCCTTGACCTCCCTGGCTCAGGGGATCCTCCTGCCTTAGCCTCCCAAATGCT ATGGCTTACTGCAGCCTTGACCTCCCTGGCTC__GGGATCCTCCTGCCTTAGCCTCCCAAATGCT CCT C GLT8D1 Ensembl:ENSG00000016864 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs575120630 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_88299,RMVar_hsa_circ_218777,RMVar_hsa_circ_49232 29760 RMVar_ID_29760 Human_SNP_ID_133346884 A-to-I Human chr3 - 52702464 52702464 52702464 ATGGCTTACTGCAGCCTTGACCTCCCTGGCTCAGGGGATCCTCCTGCCTTAGCCTCCCAAATGCT ATGGCTTACTGCAGCCTTGACCTCCCTGGCTCGGGGGATCCTCCTGCCTTAGCCTCCCAAATGCT T C GLT8D1 Ensembl:ENSG00000016864 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1246235535 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88299,RMVar_hsa_circ_218777,RMVar_hsa_circ_49232 29761 RMVar_ID_29761 Human_SNP_ID_133346885 A-to-I Human chr3 - 52702464 52702464 52702464 ATGGCTTACTGCAGCCTTGACCTCCCTGGCTCAGGGGATCCTCCTGCCTTAGCCTCCCAAATGCT ATGGCTTACTGCAGCCTTGACCTCCCTGGCTCCGGGGATCCTCCTGCCTTAGCCTCCCAAATGCT T G GLT8D1 Ensembl:ENSG00000016864 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1246235535 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88299,RMVar_hsa_circ_218777,RMVar_hsa_circ_49232 29762 RMVar_ID_29762 Human_SNP_ID_133347019 A-to-I Human chr3 - 52703051 52703051 52703051 TGTGTGGGCTGGGCCTGGTGGCTCAGGCCTGTAATCCCAGCACTTTGGAAGGCCGAGGCAGGTGG TGTGTGGGCTGGGCCTGGTGGCTCAGGCCTGTGATCCCAGCACTTTGGAAGGCCGAGGCAGGTGG T C GLT8D1 Ensembl:ENSG00000016864 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170229743 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88299,RMVar_hsa_circ_218777,RMVar_hsa_circ_49232 29763 RMVar_ID_29763 Human_SNP_ID_133348870 A-to-I Human chr3 + 52709449 52709449 52709449 ATGGGGGAAGTCAGGTGTGGTGGTTCATGCCTATAATCCCAGCACTTTCAGAGGCCGATGCAGGA ATGGGGGAAGTCAGGTGTGGTGGTTCATGCCTGTAATCCCAGCACTTTCAGAGGCCGATGCAGGA A G SPCS1 Ensembl:ENSG00000114902 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749207457 Functional Loss SNV dbSNP153 33..33 33 - - - 29764 RMVar_ID_29764 Human_SNP_ID_133351253 A-to-I Human chr3 - 52718860 52718860 52718860 CCAGCTACTTGGGAGGCTGAGGCAGGAGAATCACTTGAGCCCAGGAGGCGGAAGTCACGGTCGGT CCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAGCCCAGGAGGCGGAAGTCACGGTCGGT T C NEK4 Ensembl:ENSG00000114904 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1465693141 Functional Loss SNV dbSNP153 33..33 33 - - - 29765 RMVar_ID_29765 Human_SNP_ID_133353011 A-to-I Human chr3 - 52726354 52726354 52726354 GAGCTCGTGATTCACCTGCCTCAGCCTCCTAAAGTGCTGGGATTATAGGCGTGAGCCACTGCGCC GAGCTCGTGATTCACCTGCCTCAGCCTCCTAAGGTGCTGGGATTATAGGCGTGAGCCACTGCGCC T C NEK4 Ensembl:ENSG00000114904 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1044940118 Functional Loss SNV dbSNP153 33..33 33 - - - 29766 RMVar_ID_29766 Human_SNP_ID_133357909 A-to-I Human chr3 - 52745922 52745922 52745922 GTCCAAGAGTTCAAGACTGGCCTGGGCAATATAGTGAGACCTTGTCTCTACAAAAAATTTAAAAA GTCCAAGAGTTCAAGACTGGCCTGGGCAATATGGTGAGACCTTGTCTCTACAAAAAATTTAAAAA T C NEK4 Ensembl:ENSG00000114904 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs889029047 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_303337,RMVar_hsa_circ_335886,RMVar_hsa_circ_366361,RMVar_hsa_circ_359188,RMVar_hsa_circ_329148,RMVar_hsa_circ_333081,RMVar_hsa_circ_319327,RMVar_hsa_circ_8191,RMVar_hsa_circ_218788,RMVar_hsa_circ_218790,RMVar_hsa_circ_218791,RMVar_hsa_circ_218789,RMVar_hsa_circ_218797,RMVar_hsa_circ_364567,RMVar_hsa_circ_317855,RMVar_hsa_circ_218792,RMVar_hsa_circ_218793,RMVar_hsa_circ_218798,RMVar_hsa_circ_39075,RMVar_hsa_circ_218802,RMVar_hsa_circ_284553,RMVar_hsa_circ_318328,RMVar_hsa_circ_331739,RMVar_hsa_circ_340725,RMVar_hsa_circ_300429,RMVar_hsa_circ_218800,RMVar_hsa_circ_218801,RMVar_hsa_circ_218799,RMVar_hsa_circ_318209 29767 RMVar_ID_29767 Human_SNP_ID_133358724 A-to-I Human chr3 - 52748903 52748903 52748903 TTTTCTATTTTTTGTAGGGACAGGGTGTCCCTATGTTGTCTAGGCTGGTCTCAAACTCCTGGCTG TTTTCTATTTTTTGTAGGGACAGGGTGTCCCTGTGTTGTCTAGGCTGGTCTCAAACTCCTGGCTG T C NEK4 Ensembl:ENSG00000114904 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs994387007 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_303337,RMVar_hsa_circ_335886,RMVar_hsa_circ_366361,RMVar_hsa_circ_329148,RMVar_hsa_circ_333081,RMVar_hsa_circ_8191,RMVar_hsa_circ_218790,RMVar_hsa_circ_218791,RMVar_hsa_circ_218789,RMVar_hsa_circ_218797,RMVar_hsa_circ_317855,RMVar_hsa_circ_218792,RMVar_hsa_circ_218793,RMVar_hsa_circ_218798,RMVar_hsa_circ_39075,RMVar_hsa_circ_218802,RMVar_hsa_circ_284553,RMVar_hsa_circ_331739,RMVar_hsa_circ_340725,RMVar_hsa_circ_300429,RMVar_hsa_circ_218800,RMVar_hsa_circ_218801,RMVar_hsa_circ_318209,RMVar_hsa_circ_47060,RMVar_hsa_circ_332020,RMVar_hsa_circ_49217,RMVar_hsa_circ_23646,RMVar_hsa_circ_218803,RMVar_hsa_circ_70422 29768 RMVar_ID_29768 Human_SNP_ID_133361473 A-to-I Human chr3 - 52759039 52759039 52759039 TTACGTAGGCTGGAGTATAGTGGCATCATCATAGCTCACTACAGCCTCTGAACTCCTTGACTCAA TTACGTAGGCTGGAGTATAGTGGCATCATCATTGCTCACTACAGCCTCTGAACTCCTTGACTCAA T A NEK4 Ensembl:ENSG00000114904 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs544746558 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14895026 RMVar_hsa_circ_303337,RMVar_hsa_circ_335886,RMVar_hsa_circ_366361,RMVar_hsa_circ_329148,RMVar_hsa_circ_8191,RMVar_hsa_circ_218790,RMVar_hsa_circ_218791,RMVar_hsa_circ_218789,RMVar_hsa_circ_10780,RMVar_hsa_circ_218797,RMVar_hsa_circ_218792,RMVar_hsa_circ_218798,RMVar_hsa_circ_39075,RMVar_hsa_circ_218802,RMVar_hsa_circ_331739,RMVar_hsa_circ_340725,RMVar_hsa_circ_300429,RMVar_hsa_circ_218801,RMVar_hsa_circ_332020,RMVar_hsa_circ_49217,RMVar_hsa_circ_23646,RMVar_hsa_circ_218803,RMVar_hsa_circ_70422,RMVar_hsa_circ_361405,RMVar_hsa_circ_218806 29769 RMVar_ID_29769 Human_SNP_ID_133361474 A-to-I Human chr3 - 52759039 52759039 52759039 TTACGTAGGCTGGAGTATAGTGGCATCATCATAGCTCACTACAGCCTCTGAACTCCTTGACTCAA TTACGTAGGCTGGAGTATAGTGGCATCATCATGGCTCACTACAGCCTCTGAACTCCTTGACTCAA T C NEK4 Ensembl:ENSG00000114904 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs544746558 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14895026 RMVar_hsa_circ_303337,RMVar_hsa_circ_335886,RMVar_hsa_circ_366361,RMVar_hsa_circ_329148,RMVar_hsa_circ_8191,RMVar_hsa_circ_218790,RMVar_hsa_circ_218791,RMVar_hsa_circ_218789,RMVar_hsa_circ_10780,RMVar_hsa_circ_218797,RMVar_hsa_circ_218792,RMVar_hsa_circ_218798,RMVar_hsa_circ_39075,RMVar_hsa_circ_218802,RMVar_hsa_circ_331739,RMVar_hsa_circ_340725,RMVar_hsa_circ_300429,RMVar_hsa_circ_218801,RMVar_hsa_circ_332020,RMVar_hsa_circ_49217,RMVar_hsa_circ_23646,RMVar_hsa_circ_218803,RMVar_hsa_circ_70422,RMVar_hsa_circ_361405,RMVar_hsa_circ_218806 29770 RMVar_ID_29770 Human_SNP_ID_133408230 A-to-I Human chr3 - 52937679 52937679 52937679 ACTCAGGAGGCTGAGGTAGAAGAACCACTTGGACCCGGGAGGCGGAGGTTGCCGTGAGCTGAGAT ACTCAGGAGGCTGAGGTAGAAGAACCACTTGGTCCCGGGAGGCGGAGGTTGCCGTGAGCTGAGAT T A SFMBT1 Ensembl:ENSG00000163935 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053276103 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59022,RMVar_hsa_circ_218846,RMVar_hsa_circ_54100,RMVar_hsa_circ_375559,RMVar_hsa_circ_5991,RMVar_hsa_circ_218847,RMVar_hsa_circ_291295,RMVar_hsa_circ_4937,RMVar_hsa_circ_352196 29771 RMVar_ID_29771 Human_SNP_ID_133422455 A-to-I Human chr3 - 52995537 52995537 52995537 ACATAAACAAAGTTAGCAAGGCATGGTGGCATATGCCTGTAGTCCTAGCTACTTGGTAGGCTGAG ACATAAACAAAGTTAGCAAGGCATGGTGGCATGTGCCTGTAGTCCTAGCTACTTGGTAGGCTGAG T C SFMBT1,AC096887.1 Ensembl:ENSG00000163935,Ensembl:ENSG00000272305 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs936429105 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25746053 RMVar_hsa_circ_71215,RMVar_hsa_circ_127675,RMVar_hsa_circ_218854,RMVar_hsa_circ_349099 29772 RMVar_ID_29772 Human_SNP_ID_133422703 A-to-I Human chr3 - 52996480 52996480 52996480 GTCCGGGTGTGGTGCCTCATGCCTATAATCCTAGCATTTGGGAGGCTGAGGTGGGCAGATCGCTT GTCCGGGTGTGGTGCCTCATGCCTATAATCCTGGCATTTGGGAGGCTGAGGTGGGCAGATCGCTT T C SFMBT1,AC096887.1 Ensembl:ENSG00000163935,Ensembl:ENSG00000272305 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs951052060 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71215,RMVar_hsa_circ_127675,RMVar_hsa_circ_218854,RMVar_hsa_circ_349099 29773 RMVar_ID_29773 Human_SNP_ID_133430658 A-to-I Human chr3 - 53028590 53028590 53028590 TAGCACATTACAGCCTCCAACTCCTGGACTCAAGCTGTTTTCCCATCTCAGCCTCCCGAGTAGCT TAGCACATTACAGCCTCCAACTCCTGGACTCAGGCTGTTTTCCCATCTCAGCCTCCCGAGTAGCT T C SFMBT1,AC096887.1 Ensembl:ENSG00000163935,Ensembl:ENSG00000272305 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1028030024 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71215,RMVar_hsa_circ_127675,RMVar_hsa_circ_218854,RMVar_hsa_circ_349099 29774 RMVar_ID_29774 Human_SNP_ID_133430669 A-to-I Human chr3 - 53028665 53028665 53028665 AATTTTTTTTTAAGATGGGGTCTTGCTATGTCACCCAGACTGGAATGCAGTGACCATACACAGGT AATTTTTTTTTAAGATGGGGTCTTGCTATGTCGCCCAGACTGGAATGCAGTGACCATACACAGGT T C SFMBT1,AC096887.1 Ensembl:ENSG00000163935,Ensembl:ENSG00000272305 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904921334 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71215,RMVar_hsa_circ_127675,RMVar_hsa_circ_218854,RMVar_hsa_circ_349099 29775 RMVar_ID_29775 Human_SNP_ID_133434110 A-to-I Human chr3 - 53042400 53042400 53042400 AGGAGTTCGAGGCTGCAGTGAGCTATGATTGCACTGCTGCACTCCAGCCTGGGTAACAGAGTGAC AGGAGTTCGAGGCTGCAGTGAGCTATGATTGCGCTGCTGCACTCCAGCCTGGGTAACAGAGTGAC T C SFMBT1,AC096887.1 Ensembl:ENSG00000163935,Ensembl:ENSG00000272305 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs931467409 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25746173 RMVar_hsa_circ_71215,RMVar_hsa_circ_127675,RMVar_hsa_circ_218854,RMVar_hsa_circ_349099 29776 RMVar_ID_29776 Human_SNP_ID_133448090 A-to-I Human chr3 - 53096626 53096620 53096626 CAGGCTGGAGTACAGTGGTGTGATCTTGGCTCACTGCAGCCTCCGCCTCCCAGGTTCAAGTGATT CAGGCTGGAGTACAGTGGTGTGATCTTGGCTC______GCCTCCGCCTCCCAGGTTCAAGTGATT CTGCAGT C AC096887.1,RFT1 Ensembl:ENSG00000272305,Ensembl:ENSG00000163933 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs770822200 Functional Loss DEL dbSNP153 33..38 33 - - - 29777 RMVar_ID_29777 Human_SNP_ID_133476812 A-to-I Human chr3 - 53213455 53213455 53213455 GAGGCCATTGCTGAGGCGGGAGAACTACTTGAACCTGGGAGACGGAGGTTGCAGTGAGCCGGGAT GAGGCCATTGCTGAGGCGGGAGAACTACTTGATCCTGGGAGACGGAGGTTGCAGTGAGCCGGGAT T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1553673661 Functional Loss SNV dbSNP153 33..33 33 - - - 29778 RMVar_ID_29778 Human_SNP_ID_133477615 A-to-I Human chr3 - 53216467 53216467 53216467 GCCAGGCTGGTCTCGAACTCCTGACTTCAAGTAATCTGCCCTCCTTGGTCTTCCAAAGTGATGGG GCCAGGCTGGTCTCGAACTCCTGACTTCAAGTCATCTGCCCTCCTTGGTCTTCCAAAGTGATGGG T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1353293314 Functional Loss SNV dbSNP153 33..33 33 - - - 29779 RMVar_ID_29779 Human_SNP_ID_133478454 A-to-I Human chr3 - 53219572 53219572 53219572 CCACCTCAGCCTTTCCAGTAGCTGAGACTACAAACGTGCGCCACCGCACCCAGTTTGCTTTTATT CCACCTCAGCCTTTCCAGTAGCTGAGACTACAGACGTGCGCCACCGCACCCAGTTTGCTTTTATT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1344842682 Functional Loss SNV dbSNP153 33..33 33 - - - 29780 RMVar_ID_29780 Human_SNP_ID_133478663 A-to-I Human chr3 - 53220477 53220477 53220477 AGCTCAAGCAATCCACCAGTCTTGGCCTCCCAAAGTGCTCGGATTACAGGTGTGAGCTGCTGCGT AGCTCAAGCAATCCACCAGTCTTGGCCTCCCAGAGTGCTCGGATTACAGGTGTGAGCTGCTGCGT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1406134979 Functional Loss SNV dbSNP153 33..33 33 - - - 29781 RMVar_ID_29781 Human_SNP_ID_133478664 A-to-I Human chr3 - 53220477 53220477 53220477 AGCTCAAGCAATCCACCAGTCTTGGCCTCCCAAAGTGCTCGGATTACAGGTGTGAGCTGCTGCGT AGCTCAAGCAATCCACCAGTCTTGGCCTCCCACAGTGCTCGGATTACAGGTGTGAGCTGCTGCGT T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1406134979 Functional Loss SNV dbSNP153 33..33 33 - - - 29782 RMVar_ID_29782 Human_SNP_ID_133478668 A-to-I Human chr3 - 53220503 53220503 53220503 TTGCTCAGGCTGGTCTCGAACTCGTGAGCTCAAGCAATCCACCAGTCTTGGCCTCCCAAAGTGCT TTGCTCAGGCTGGTCTCGAACTCGTGAGCTCAGGCAATCCACCAGTCTTGGCCTCCCAAAGTGCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1346011899 Functional Loss SNV dbSNP153 33..33 33 - - - 29783 RMVar_ID_29783 Human_SNP_ID_133482298 A-to-I Human chr3 - 53233209 53233209 53233209 GGAGGAGCTGTGCAAGGCCTTTGGCCAGGCCAAGCACCAGCCAACAGCCATCATTGCCAAGACCT GGAGGAGCTGTGCAAGGCCTTTGGCCAGGCCAGGCACCAGCCAACAGCCATCATTGCCAAGACCT T C TKT Ensembl:ENSG00000163931 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs782145199 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247614,Human_RBP_ID_937256,Human_RBP_ID_8576487,Human_RBP_ID_18194638,Human_RBP_ID_22455979,Human_RBP_ID_22769316,Human_RBP_ID_26824800,Human_RBP_ID_27159892,Human_RBP_ID_27321308,Human_RBP_ID_27504016 Human_Splice_Rec_441180,Human_Splice_Rec_441181,Human_Splice_Rec_441206,Human_Splice_Rec_441207,Human_Splice_Rec_441258,Human_Splice_Rec_441259,Human_Splice_Rec_441286,Human_Splice_Rec_441287,Human_Splice_Rec_441310,Human_Splice_Rec_441311,Human_Splice_Rec_441336,Human_Splice_Rec_441337,Human_Splice_Rec_441366,Human_Splice_Rec_441367,Human_Splice_Rec_441369,Human_Splice_Rec_441372 Human_miRNA_ID_140215,Human_miRNA_ID_417180,Human_miRNA_ID_2050730 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_218886,RMVar_hsa_circ_218884,RMVar_hsa_circ_218885,RMVar_hsa_circ_281638,RMVar_hsa_circ_301729 29784 RMVar_ID_29784 Human_SNP_ID_133482299 A-to-I Human chr3 - 53233209 53233209 53233209 GGAGGAGCTGTGCAAGGCCTTTGGCCAGGCCAAGCACCAGCCAACAGCCATCATTGCCAAGACCT GGAGGAGCTGTGCAAGGCCTTTGGCCAGGCCACGCACCAGCCAACAGCCATCATTGCCAAGACCT T G TKT Ensembl:ENSG00000163931 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs782145199 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247614,Human_RBP_ID_937256,Human_RBP_ID_8576487,Human_RBP_ID_18194638,Human_RBP_ID_22455979,Human_RBP_ID_22769316,Human_RBP_ID_26824800,Human_RBP_ID_27159892,Human_RBP_ID_27321308,Human_RBP_ID_27504016 Human_Splice_Rec_441180,Human_Splice_Rec_441181,Human_Splice_Rec_441206,Human_Splice_Rec_441207,Human_Splice_Rec_441258,Human_Splice_Rec_441259,Human_Splice_Rec_441286,Human_Splice_Rec_441287,Human_Splice_Rec_441310,Human_Splice_Rec_441311,Human_Splice_Rec_441336,Human_Splice_Rec_441337,Human_Splice_Rec_441366,Human_Splice_Rec_441367,Human_Splice_Rec_441369,Human_Splice_Rec_441372 Human_miRNA_ID_140215,Human_miRNA_ID_417180,Human_miRNA_ID_2050730 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_218886,RMVar_hsa_circ_218884,RMVar_hsa_circ_218885,RMVar_hsa_circ_281638,RMVar_hsa_circ_301729 29785 RMVar_ID_29785 Human_SNP_ID_133486717 A-to-I Human chr3 - 53249249 53249232 53249249 AACAAATTTTTAGGCCAGGTGTGATAGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGT AACAAATTTTTAGGCCAGGTGTGATAGCTCAC_________________TTTGGGAGGCCAAGGT AGTGCTGGGATTACAGGT A TKT Ensembl:ENSG00000163931 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432265381 Functional Loss DEL dbSNP153 33..49 33 - - - RMVar_hsa_circ_91143,RMVar_hsa_circ_218889 29786 RMVar_ID_29786 Human_SNP_ID_133486721 A-to-I Human chr3 - 53249256 53249256 53249256 TTTTAAAAACAAATTTTTAGGCCAGGTGTGATAGCTCACACCTGTAATCCCAGCACTTTGGGAGG TTTTAAAAACAAATTTTTAGGCCAGGTGTGATGGCTCACACCTGTAATCCCAGCACTTTGGGAGG T C TKT Ensembl:ENSG00000163931 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs920040712 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91143,RMVar_hsa_circ_218889 29787 RMVar_ID_29787 Human_SNP_ID_133486998 A-to-I Human chr3 - 53250545 53250545 53250545 GCTGGTCTCAAACTCCTGGGCTTAAGCGATCCACCTGCCTCAGCTTCCCTAGAGTACTGGGATTA GCTGGTCTCAAACTCCTGGGCTTAAGCGATCCCCCTGCCTCAGCTTCCCTAGAGTACTGGGATTA T G TKT Ensembl:ENSG00000163931 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1483305734 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91143,RMVar_hsa_circ_218889 29788 RMVar_ID_29788 Human_SNP_ID_133487013 A-to-I Human chr3 - 53250605 53250605 53250605 ACTATGCCTTGGCTAATTTTTGTATTTTTTGTAGAGTTGAGGTTTTGTCATTTTGCCCAGGCTGG ACTATGCCTTGGCTAATTTTTGTATTTTTTGTGGAGTTGAGGTTTTGTCATTTTGCCCAGGCTGG T C TKT Ensembl:ENSG00000163931 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs797033362 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14900332 RMVar_hsa_circ_91143,RMVar_hsa_circ_218889 29789 RMVar_ID_29789 Human_SNP_ID_133487031 A-to-I Human chr3 - 53250688 53250688 53250688 TGCTCACTGCAGCCTCCGCCTCCTGGGCTCAAATGATGCCCTCATCTCAGCCTCACAAGTAGCTG TGCTCACTGCAGCCTCCGCCTCCTGGGCTCAAGTGATGCCCTCATCTCAGCCTCACAAGTAGCTG T C TKT Ensembl:ENSG00000163931 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1330290761 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91143,RMVar_hsa_circ_218889 29790 RMVar_ID_29790 Human_SNP_ID_133487084 A-to-I Human chr3 - 53250920 53250920 53250920 CAAAAAAAAGAAAGAGCTGTGCATGTGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGTGTGAGG CAAAAAAAAGAAAGAGCTGTGCATGTGCCTGTGGTCCCAGCTACTTGGGAGGCTGAGGTGTGAGG T C TKT Ensembl:ENSG00000163931 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs964999864 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91143,RMVar_hsa_circ_218889 29791 RMVar_ID_29791 Human_SNP_ID_133487104 A-to-I Human chr3 - 53250974 53250974 53250974 TTGAGCCTGGGAGTTCAGGACCAAACTGGGCAACATAGTGAGACCTCATCTCTACAAAAAAAAGA TTGAGCCTGGGAGTTCAGGACCAAACTGGGCAGCATAGTGAGACCTCATCTCTACAAAAAAAAGA T C TKT Ensembl:ENSG00000163931 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs937548672 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8576516 RMVar_hsa_circ_91143,RMVar_hsa_circ_218889 29792 RMVar_ID_29792 Human_SNP_ID_133487768 A-to-I Human chr3 - 53253875 53253875 53253875 CTTCTTGGCAGGGCATGGTGGTTCATGCCTGTAATCACAGCACTTTGGGAGGCCAAGGTGGGAGG CTTCTTGGCAGGGCATGGTGGTTCATGCCTGTGATCACAGCACTTTGGGAGGCCAAGGTGGGAGG T C TKT Ensembl:ENSG00000163931 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1265377545 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91143,RMVar_hsa_circ_218889 29793 RMVar_ID_29793 Human_SNP_ID_133496549 A-to-I Human chr3 - 53289256 53289256 53289256 TACATAAACTGAAATGCAGATTTTTAGAGGCCAGGTGTGGTGGCTCATGCCTGTAACCCCAGCAC TACATAAACTGAAATGCAGATTTTTAGAGGCCGGGTGTGGTGGCTCATGCCTGTAACCCCAGCAC T C DCP1A Ensembl:ENSG00000272886 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334209747 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14455,RMVar_hsa_circ_320801,RMVar_hsa_circ_329185,RMVar_hsa_circ_23094,RMVar_hsa_circ_12674 29794 RMVar_ID_29794 Human_SNP_ID_133501483 A-to-I Human chr3 - 53308896 53308896 53308896 CAGGGTATTTTTGTTCTTAAAAAATAGAGGCCAGACACAGTGACTCATGCCCATAATTCCAGCAC CAGGGTATTTTTGTTCTTAAAAAATAGAGGCCGGACACAGTGACTCATGCCCATAATTCCAGCAC T C DCP1A Ensembl:ENSG00000272886 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs939873421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14901108 RMVar_hsa_circ_5203,RMVar_hsa_circ_14455,RMVar_hsa_circ_320801,RMVar_hsa_circ_287095 29795 RMVar_ID_29795 Human_SNP_ID_133501651 A-to-I Human chr3 - 53309515 53309515 53309515 GCTCAAGCTGTCCTCCCGCCTTGGCCTCCCAAAGTGCTGGAATTATAGGTGTGAGACACTGTGGC GCTCAAGCTGTCCTCCCGCCTTGGCCTCCCAAGGTGCTGGAATTATAGGTGTGAGACACTGTGGC T C DCP1A Ensembl:ENSG00000272886 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1553688426 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17573690 RMVar_hsa_circ_5203,RMVar_hsa_circ_14455,RMVar_hsa_circ_320801,RMVar_hsa_circ_287095 29796 RMVar_ID_29796 Human_SNP_ID_133503124 A-to-I Human chr3 - 53315438 53315432 53315438 GCCCTCCTGGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAAGTGCCTG GCCCTCCTGGGTTCAAGCAGTTCTCCTGCCTC______CCGAGTAGCTGGGATTACAAGTGCCTG GGAGGCT G DCP1A Ensembl:ENSG00000272886 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1403752467 Functional Loss DEL dbSNP153 33..38 33 - - - RMVar_hsa_circ_320801,RMVar_hsa_circ_287095,RMVar_hsa_circ_11277,RMVar_hsa_circ_273525 29797 RMVar_ID_29797 Human_SNP_ID_133586013 A-to-I Human chr3 + 53662367 53662367 53662367 CCTGGAGACCAGGCCTTCTGACCCCTGTGTTGACGTCCCCCATTCTCTCCACAGCCCCGCGACCT CCTGGAGACCAGGCCTTCTGACCCCTGTGTTGTCGTCCCCCATTCTCTCCACAGCCCCGCGACCT A T CACNA1D Ensembl:ENSG00000157388 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs764839653 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21751,RMVar_hsa_circ_101828,RMVar_hsa_circ_218894,RMVar_hsa_circ_270299,RMVar_hsa_circ_75203,RMVar_hsa_circ_339214,RMVar_hsa_circ_327551,RMVar_hsa_circ_57512,RMVar_hsa_circ_218898 29798 RMVar_ID_29798 Human_SNP_ID_133586020 A-to-I Human chr3 + 53662387 53662387 53662387 ACCCCTGTGTTGACGTCCCCCATTCTCTCCACAGCCCCGCGACCTCAGCACTACTGTGCTGCTCA ACCCCTGTGTTGACGTCCCCCATTCTCTCCACGGCCCCGCGACCTCAGCACTACTGTGCTGCTCA A G CACNA1D Ensembl:ENSG00000157388 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs564240448 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21751,RMVar_hsa_circ_101828,RMVar_hsa_circ_218894,RMVar_hsa_circ_270299,RMVar_hsa_circ_75203,RMVar_hsa_circ_339214,RMVar_hsa_circ_327551,RMVar_hsa_circ_57512,RMVar_hsa_circ_218898 29799 RMVar_ID_29799 Human_SNP_ID_133586021 A-to-I Human chr3 + 53662387 53662387 53662387 ACCCCTGTGTTGACGTCCCCCATTCTCTCCACAGCCCCGCGACCTCAGCACTACTGTGCTGCTCA ACCCCTGTGTTGACGTCCCCCATTCTCTCCACTGCCCCGCGACCTCAGCACTACTGTGCTGCTCA A T CACNA1D Ensembl:ENSG00000157388 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs564240448 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21751,RMVar_hsa_circ_101828,RMVar_hsa_circ_218894,RMVar_hsa_circ_270299,RMVar_hsa_circ_75203,RMVar_hsa_circ_339214,RMVar_hsa_circ_327551,RMVar_hsa_circ_57512,RMVar_hsa_circ_218898 29800 RMVar_ID_29800 Human_SNP_ID_133586276 A-to-I Human chr3 + 53663423 53663423 53663423 GAGCAGCACAGTCGTGCTGAGGTCGTGGGGCCATGGAGAGGATGGGGGATGCCAATGCAAGGTCA GAGCAGCACAGTCGTGCTGAGGTCGTGGGGCCGTGGAGAGGATGGGGGATGCCAATGCAAGGTCA A G CACNA1D Ensembl:ENSG00000157388 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs757796074 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21751,RMVar_hsa_circ_101828,RMVar_hsa_circ_218894,RMVar_hsa_circ_270299,RMVar_hsa_circ_75203,RMVar_hsa_circ_339214,RMVar_hsa_circ_327551,RMVar_hsa_circ_57512,RMVar_hsa_circ_218898 29801 RMVar_ID_29801 Human_SNP_ID_133623633 A-to-I Human chr3 + 53812342 53812342 53812342 TCGGGCTATCCAGAAGTAGAAGAAATAGAGCCAATTCTCATTTATTCAGCGAAAATCCTCTGGGG TCGGGCTATCCAGAAGTAGAAGAAATAGAGCCGATTCTCATTTATTCAGCGAAAATCCTCTGGGG A G CACNA1D Ensembl:ENSG00000157388 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs781612090 Functional Loss SNV dbSNP153 33..33 33 - - - 29802 RMVar_ID_29802 Human_SNP_ID_133623634 A-to-I Human chr3 + 53812342 53812342 53812342 TCGGGCTATCCAGAAGTAGAAGAAATAGAGCCAATTCTCATTTATTCAGCGAAAATCCTCTGGGG TCGGGCTATCCAGAAGTAGAAGAAATAGAGCCTATTCTCATTTATTCAGCGAAAATCCTCTGGGG A T CACNA1D Ensembl:ENSG00000157388 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs781612090 Functional Loss SNV dbSNP153 33..33 33 - - - 29803 RMVar_ID_29803 Human_SNP_ID_133637046 A-to-I Human chr3 - 53863883 53863883 53863883 AGGAGGCAGAGGTTGCAGTGAGCCAAGATCACACCATTCCACTCCAGCCTGGGCAACAGAGTGAG AGGAGGCAGAGGTTGCAGTGAGCCAAGATCACGCCATTCCACTCCAGCCTGGGCAACAGAGTGAG T C - - Other Unknown GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1460255853 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4750707 29804 RMVar_ID_29804 Human_SNP_ID_133637047 A-to-I Human chr3 - 53863883 53863883 53863883 AGGAGGCAGAGGTTGCAGTGAGCCAAGATCACACCATTCCACTCCAGCCTGGGCAACAGAGTGAG AGGAGGCAGAGGTTGCAGTGAGCCAAGATCACCCCATTCCACTCCAGCCTGGGCAACAGAGTGAG T G - - Other Unknown GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1460255853 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4750707 29805 RMVar_ID_29805 Human_SNP_ID_133637051 A-to-I Human chr3 - 53863908 53863907 53863908 TAAGGTGGGAGGTTCACTTGAGCTCAGGAGGCAGAGGTTGCAGTGAGCCAAGATCACACCATTCC TAAGGTGGGAGGTTCACTTGAGCTCAGGAGGC_GAGGTTGCAGTGAGCCAAGATCACACCATTCC CT C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1379163042 Functional Loss DEL dbSNP153 33..33 33 - - - 29806 RMVar_ID_29806 Human_SNP_ID_133637075 A-to-I Human chr3 - 53863996 53863996 53863996 CAACATGGCGAAACCCCATCTCAACAAAAAGTACAAATATTAGCTGGGCTTGATGGCATGCATCT CAACATGGCGAAACCCCATCTCAACAAAAAGTGCAAATATTAGCTGGGCTTGATGGCATGCATCT T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs937620072 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25746584 29807 RMVar_ID_29807 Human_SNP_ID_133637083 A-to-I Human chr3 - 53864065 53864065 53864065 GAATCCCAGCACTTTGGGAGGCCAAGGCTGGTAGATCACTTGAGTCCAGGAGTTCCAGACCAGCC GAATCCCAGCACTTTGGGAGGCCAAGGCTGGTGGATCACTTGAGTCCAGGAGTTCCAGACCAGCC T C - - Other Unknown GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs896184368 Functional Loss SNV dbSNP153 33..33 33 - - - 29808 RMVar_ID_29808 Human_SNP_ID_133637693 A-to-I Human chr3 - 53866228 53866228 53866228 AGGCTTACACCATCACACTCAGCTAATTTTTTAAATCTTTTGTAGAGATGGAGGTCTCGCTTTGT AGGCTTACACCATCACACTCAGCTAATTTTTTTAATCTTTTGTAGAGATGGAGGTCTCGCTTTGT T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1156433023 Functional Loss SNV dbSNP153 33..33 33 - - - 29809 RMVar_ID_29809 Human_SNP_ID_133637834 A-to-I Human chr3 - 53866662 53866653 53866663 CCTGGCTAACAGGGTGAAACCCCGTCTCTACTAAAAATATAAAAAGTTAGCTGGGTGTGGTGGTG CCTGGCTAACAGGGTGAAACCCCGTCTCTAC__________AAAAGTTAGCTGGGTGTGGTGGTG TTATATTTTTA T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs77479324 Functional Loss DEL dbSNP153 32..41 33 - - - 29810 RMVar_ID_29810 Human_SNP_ID_133637835 A-to-I Human chr3 - 53866662 53866654 53866663 CCTGGCTAACAGGGTGAAACCCCGTCTCTACTAAAAATATAAAAAGTTAGCTGGGTGTGGTGGTG CCTGGCTAACAGGGTGAAACCCCGTCTCTAC_________AAAAAGTTAGCTGGGTGTGGTGGTG TATATTTTTA T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs58065023 Functional Loss DEL dbSNP153 32..40 33 - - - GWAS_ID_3240,GWAS_ID_3241,GWAS_ID_3242,GWAS_ID_3243,GWAS_ID_3244,GWAS_ID_3245,GWAS_ID_3246,GWAS_ID_3247,GWAS_ID_3248,GWAS_ID_3249,GWAS_ID_3250 29811 RMVar_ID_29811 Human_SNP_ID_134321147 A-to-I Human chr3 + 56563240 56563240 56563240 AAAACTAGCCAGGCTTGGTGGTGGGCACCTGTAATCCCAGCTACTCAGGTGGCTGAGGCAGGAGA AAAACTAGCCAGGCTTGGTGGTGGGCACCTGTGATCCCAGCTACTCAGGTGGCTGAGGCAGGAGA A G CCDC66 Ensembl:ENSG00000180376 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs567176968 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45306,RMVar_hsa_circ_324762,RMVar_hsa_circ_218992,RMVar_hsa_circ_33746,RMVar_hsa_circ_38682,RMVar_hsa_circ_21644 29812 RMVar_ID_29812 Human_SNP_ID_134322156 A-to-I Human chr3 + 56566377 56566377 56566377 GAACTCCTGAGCTTAAGCAATCTGCCCACGTCAGCCTTCCAAAGTTCTGGGACTACAGGTGTGAG GAACTCCTGAGCTTAAGCAATCTGCCCACGTCCGCCTTCCAAAGTTCTGGGACTACAGGTGTGAG A C CCDC66 Ensembl:ENSG00000180376 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs902520948 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14904043 RMVar_hsa_circ_218994,RMVar_hsa_circ_45306,RMVar_hsa_circ_324762,RMVar_hsa_circ_22368,RMVar_hsa_circ_218992,RMVar_hsa_circ_33746,RMVar_hsa_circ_38682,RMVar_hsa_circ_21644,RMVar_hsa_circ_283419,RMVar_hsa_circ_320932,RMVar_hsa_circ_359599,RMVar_hsa_circ_367658,RMVar_hsa_circ_310699,RMVar_hsa_circ_59335,RMVar_hsa_circ_279743,RMVar_hsa_circ_53876,RMVar_hsa_circ_5976,RMVar_hsa_circ_10279,RMVar_hsa_circ_218995,RMVar_hsa_circ_218996,RMVar_hsa_circ_218997,RMVar_hsa_circ_218993 29813 RMVar_ID_29813 Human_SNP_ID_134322485 A-to-I Human chr3 + 56567355 56567355 56567355 GAGGTTGCAGTGAGCCAAGATCGTGCCACTGCACTCCAGCTGGGCTACCGAGCAAGACTCCATCT GAGGTTGCAGTGAGCCAAGATCGTGCCACTGCCCTCCAGCTGGGCTACCGAGCAAGACTCCATCT A C CCDC66 Ensembl:ENSG00000180376 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs530982713 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_156215 RMVar_hsa_circ_218994,RMVar_hsa_circ_45306,RMVar_hsa_circ_324762,RMVar_hsa_circ_22368,RMVar_hsa_circ_218992,RMVar_hsa_circ_33746,RMVar_hsa_circ_38682,RMVar_hsa_circ_283419,RMVar_hsa_circ_320932,RMVar_hsa_circ_359599,RMVar_hsa_circ_367658,RMVar_hsa_circ_310699,RMVar_hsa_circ_59335,RMVar_hsa_circ_53876,RMVar_hsa_circ_5976,RMVar_hsa_circ_10279,RMVar_hsa_circ_218995,RMVar_hsa_circ_218996,RMVar_hsa_circ_54935,RMVar_hsa_circ_330996,RMVar_hsa_circ_344231,RMVar_hsa_circ_320913,RMVar_hsa_circ_349859,RMVar_hsa_circ_218999,RMVar_hsa_circ_218998,RMVar_hsa_circ_363721,RMVar_hsa_circ_309098,RMVar_hsa_circ_268604,RMVar_hsa_circ_219002 29814 RMVar_ID_29814 Human_SNP_ID_134323146 A-to-I Human chr3 + 56569899 56569899 56569899 TCTTGTTGCCCAAGCTGGAGTGCAATGGCACCATCTCAGCTCACTGCAACCTCTGCTTGCTGGGT TCTTGTTGCCCAAGCTGGAGTGCAATGGCACCGTCTCAGCTCACTGCAACCTCTGCTTGCTGGGT A G CCDC66 Ensembl:ENSG00000180376 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs918430292 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_218994,RMVar_hsa_circ_45306,RMVar_hsa_circ_324762,RMVar_hsa_circ_22368,RMVar_hsa_circ_218992,RMVar_hsa_circ_33746,RMVar_hsa_circ_38682,RMVar_hsa_circ_283419,RMVar_hsa_circ_320932,RMVar_hsa_circ_359599,RMVar_hsa_circ_367658,RMVar_hsa_circ_310699,RMVar_hsa_circ_59335,RMVar_hsa_circ_53876,RMVar_hsa_circ_5976,RMVar_hsa_circ_10279,RMVar_hsa_circ_218995,RMVar_hsa_circ_218996,RMVar_hsa_circ_54935,RMVar_hsa_circ_330996,RMVar_hsa_circ_344231,RMVar_hsa_circ_320913,RMVar_hsa_circ_349859,RMVar_hsa_circ_218999,RMVar_hsa_circ_218998,RMVar_hsa_circ_363721,RMVar_hsa_circ_309098,RMVar_hsa_circ_268604,RMVar_hsa_circ_219002 29815 RMVar_ID_29815 Human_SNP_ID_134323162 A-to-I Human chr3 + 56569964 56569964 56569964 TCAAGTGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCACCTGCCACCATGCCCA TCAAGTGATTCTCCTGCCTCAGCCTCCTGAGTGGCTGGGATTACAGGCACCTGCCACCATGCCCA A G CCDC66 Ensembl:ENSG00000180376 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs973522522 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_218994,RMVar_hsa_circ_45306,RMVar_hsa_circ_324762,RMVar_hsa_circ_22368,RMVar_hsa_circ_218992,RMVar_hsa_circ_33746,RMVar_hsa_circ_38682,RMVar_hsa_circ_283419,RMVar_hsa_circ_320932,RMVar_hsa_circ_359599,RMVar_hsa_circ_367658,RMVar_hsa_circ_310699,RMVar_hsa_circ_59335,RMVar_hsa_circ_53876,RMVar_hsa_circ_5976,RMVar_hsa_circ_10279,RMVar_hsa_circ_218995,RMVar_hsa_circ_218996,RMVar_hsa_circ_54935,RMVar_hsa_circ_330996,RMVar_hsa_circ_344231,RMVar_hsa_circ_320913,RMVar_hsa_circ_349859,RMVar_hsa_circ_218999,RMVar_hsa_circ_218998,RMVar_hsa_circ_363721,RMVar_hsa_circ_309098,RMVar_hsa_circ_268604,RMVar_hsa_circ_219002 29816 RMVar_ID_29816 Human_SNP_ID_134323174 A-to-I Human chr3 + 56570064 56570064 56570064 CACCATGTTGGCCAGGCTGGTCTCAAACTCCTAACCTCAGGTGATCCGCCTGCCTTGGCCTCCCG CACCATGTTGGCCAGGCTGGTCTCAAACTCCTGACCTCAGGTGATCCGCCTGCCTTGGCCTCCCG A G CCDC66 Ensembl:ENSG00000180376 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1416066633 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18812476 RMVar_hsa_circ_218994,RMVar_hsa_circ_45306,RMVar_hsa_circ_324762,RMVar_hsa_circ_22368,RMVar_hsa_circ_218992,RMVar_hsa_circ_33746,RMVar_hsa_circ_38682,RMVar_hsa_circ_283419,RMVar_hsa_circ_320932,RMVar_hsa_circ_359599,RMVar_hsa_circ_367658,RMVar_hsa_circ_310699,RMVar_hsa_circ_59335,RMVar_hsa_circ_53876,RMVar_hsa_circ_5976,RMVar_hsa_circ_10279,RMVar_hsa_circ_218995,RMVar_hsa_circ_218996,RMVar_hsa_circ_54935,RMVar_hsa_circ_330996,RMVar_hsa_circ_344231,RMVar_hsa_circ_320913,RMVar_hsa_circ_349859,RMVar_hsa_circ_218999,RMVar_hsa_circ_218998,RMVar_hsa_circ_363721,RMVar_hsa_circ_309098,RMVar_hsa_circ_268604,RMVar_hsa_circ_219002 29817 RMVar_ID_29817 Human_SNP_ID_134323275 A-to-I Human chr3 + 56570543 56570543 56570543 GGAGGCCGAGGCAGGTGGATCACAAGGTCAGGAAATAGAGACCATCCTAGCCAACATGGTGAAAC GGAGGCCGAGGCAGGTGGATCACAAGGTCAGGGAATAGAGACCATCCTAGCCAACATGGTGAAAC A G CCDC66 Ensembl:ENSG00000180376 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1027850344 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5206615 RMVar_hsa_circ_218994,RMVar_hsa_circ_45306,RMVar_hsa_circ_324762,RMVar_hsa_circ_22368,RMVar_hsa_circ_218992,RMVar_hsa_circ_33746,RMVar_hsa_circ_38682,RMVar_hsa_circ_283419,RMVar_hsa_circ_320932,RMVar_hsa_circ_359599,RMVar_hsa_circ_367658,RMVar_hsa_circ_310699,RMVar_hsa_circ_59335,RMVar_hsa_circ_53876,RMVar_hsa_circ_5976,RMVar_hsa_circ_10279,RMVar_hsa_circ_218995,RMVar_hsa_circ_218996,RMVar_hsa_circ_54935,RMVar_hsa_circ_330996,RMVar_hsa_circ_344231,RMVar_hsa_circ_320913,RMVar_hsa_circ_349859,RMVar_hsa_circ_218999,RMVar_hsa_circ_218998,RMVar_hsa_circ_363721,RMVar_hsa_circ_309098,RMVar_hsa_circ_268604,RMVar_hsa_circ_219002 29818 RMVar_ID_29818 Human_SNP_ID_134323278 A-to-I Human chr3 + 56570547 56570547 56570547 GCCGAGGCAGGTGGATCACAAGGTCAGGAAATAGAGACCATCCTAGCCAACATGGTGAAACCACA GCCGAGGCAGGTGGATCACAAGGTCAGGAAATGGAGACCATCCTAGCCAACATGGTGAAACCACA A G CCDC66 Ensembl:ENSG00000180376 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs998483248 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_218994,RMVar_hsa_circ_45306,RMVar_hsa_circ_324762,RMVar_hsa_circ_22368,RMVar_hsa_circ_218992,RMVar_hsa_circ_33746,RMVar_hsa_circ_38682,RMVar_hsa_circ_283419,RMVar_hsa_circ_320932,RMVar_hsa_circ_359599,RMVar_hsa_circ_367658,RMVar_hsa_circ_310699,RMVar_hsa_circ_59335,RMVar_hsa_circ_53876,RMVar_hsa_circ_5976,RMVar_hsa_circ_10279,RMVar_hsa_circ_218995,RMVar_hsa_circ_218996,RMVar_hsa_circ_54935,RMVar_hsa_circ_330996,RMVar_hsa_circ_344231,RMVar_hsa_circ_320913,RMVar_hsa_circ_349859,RMVar_hsa_circ_218999,RMVar_hsa_circ_218998,RMVar_hsa_circ_363721,RMVar_hsa_circ_309098,RMVar_hsa_circ_268604,RMVar_hsa_circ_219002 29819 RMVar_ID_29819 Human_SNP_ID_134323324 A-to-I Human chr3 + 56570702 56570702 56570702 CCTGGGAGGCGGAGATTGCAGTGAGCTGAGATAGCGCCATTGCACTCCAGGCTGCTGACAGAATG CCTGGGAGGCGGAGATTGCAGTGAGCTGAGATGGCGCCATTGCACTCCAGGCTGCTGACAGAATG A G CCDC66 Ensembl:ENSG00000180376 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs566965250 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_218994,RMVar_hsa_circ_45306,RMVar_hsa_circ_324762,RMVar_hsa_circ_22368,RMVar_hsa_circ_218992,RMVar_hsa_circ_33746,RMVar_hsa_circ_38682,RMVar_hsa_circ_283419,RMVar_hsa_circ_320932,RMVar_hsa_circ_359599,RMVar_hsa_circ_367658,RMVar_hsa_circ_310699,RMVar_hsa_circ_59335,RMVar_hsa_circ_53876,RMVar_hsa_circ_5976,RMVar_hsa_circ_10279,RMVar_hsa_circ_218995,RMVar_hsa_circ_218996,RMVar_hsa_circ_54935,RMVar_hsa_circ_330996,RMVar_hsa_circ_344231,RMVar_hsa_circ_320913,RMVar_hsa_circ_349859,RMVar_hsa_circ_218999,RMVar_hsa_circ_218998,RMVar_hsa_circ_363721,RMVar_hsa_circ_309098,RMVar_hsa_circ_268604,RMVar_hsa_circ_219002 29820 RMVar_ID_29820 Human_SNP_ID_134335661 A-to-I Human chr3 + 56617341 56617336 56617341 TGTAATCAGTTCACAAGAATAGAGAAACAAACAAAACACATGAAGAAATATCCTAAAAGGCCTGA TGTAATCAGTTCACAAGAATAGAGAAAC_____AAACACATGAAGAAATATCCTAAAAGGCCTGA CAAACA C CCDC66 Ensembl:ENSG00000180376 Protein coding CDS GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs750927810 Functional Loss DEL dbSNP153 29..33 33 - - - Human_RBP_ID_18536013 RMVar_hsa_circ_38682,RMVar_hsa_circ_359599,RMVar_hsa_circ_59335,RMVar_hsa_circ_10279,RMVar_hsa_circ_268604,RMVar_hsa_circ_56908,RMVar_hsa_circ_80273,RMVar_hsa_circ_219007,RMVar_hsa_circ_50969,RMVar_hsa_circ_52166,RMVar_hsa_circ_219008,RMVar_hsa_circ_10173,RMVar_hsa_circ_344723 29821 RMVar_ID_29821 Human_SNP_ID_134338445 A-to-I Human chr3 - 56625404 56625404 56625404 ATCTCAGGTGATCCAACTGCTTTGGCCTCCCAAAGTTTTGGGATTACAGGTGTGAGCCACCAGGC ATCTCAGGTGATCCAACTGCTTTGGCCTCCCAGAGTTTTGGGATTACAGGTGTGAGCCACCAGGC T C TASOR Ensembl:ENSG00000163946 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017649531 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5216,RMVar_hsa_circ_99242,RMVar_hsa_circ_268574,RMVar_hsa_circ_219011,RMVar_hsa_circ_219010,RMVar_hsa_circ_219012,RMVar_hsa_circ_298677,RMVar_hsa_circ_219013,RMVar_hsa_circ_219014,RMVar_hsa_circ_309610,RMVar_hsa_circ_376571,RMVar_hsa_circ_379023,RMVar_hsa_circ_302644,RMVar_hsa_circ_267678,RMVar_hsa_circ_269199,RMVar_hsa_circ_100147,RMVar_hsa_circ_219015,RMVar_hsa_circ_219017,RMVar_hsa_circ_219018,RMVar_hsa_circ_219019,RMVar_hsa_circ_219016 29822 RMVar_ID_29822 Human_SNP_ID_134339688 A-to-I Human chr3 - 56630130 56630130 56630130 AAACCCCGTCTCTACTAAAAATACAAAAAATTAGCCAGGCATGGTGGTGGGTGCCTGTAGTCCCA AAACCCCGTCTCTACTAAAAATACAAAAAATTGGCCAGGCATGGTGGTGGGTGCCTGTAGTCCCA T C TASOR Ensembl:ENSG00000163946 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs977763156 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5216,RMVar_hsa_circ_99242,RMVar_hsa_circ_268574,RMVar_hsa_circ_219010,RMVar_hsa_circ_219012,RMVar_hsa_circ_298677,RMVar_hsa_circ_219014,RMVar_hsa_circ_379023,RMVar_hsa_circ_302644,RMVar_hsa_circ_267678,RMVar_hsa_circ_269199,RMVar_hsa_circ_100147,RMVar_hsa_circ_6963,RMVar_hsa_circ_219015,RMVar_hsa_circ_219017,RMVar_hsa_circ_219018,RMVar_hsa_circ_219016,RMVar_hsa_circ_219022,RMVar_hsa_circ_83246,RMVar_hsa_circ_362275,RMVar_hsa_circ_91145,RMVar_hsa_circ_40140,RMVar_hsa_circ_219023,RMVar_hsa_circ_113851,RMVar_hsa_circ_268263,RMVar_hsa_circ_12624,RMVar_hsa_circ_37017,RMVar_hsa_circ_219024 29823 RMVar_ID_29823 Human_SNP_ID_134339829 A-to-I Human chr3 - 56630735 56630735 56630735 GGTCAAGCAATTCTCCTGCCTCATCCTCCCAAATAGCTGGGATTGCAGGCACCCGCCACCACTCC GGTCAAGCAATTCTCCTGCCTCATCCTCCCAAGTAGCTGGGATTGCAGGCACCCGCCACCACTCC T C TASOR Ensembl:ENSG00000163946 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1559816558 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5216,RMVar_hsa_circ_99242,RMVar_hsa_circ_268574,RMVar_hsa_circ_219010,RMVar_hsa_circ_219012,RMVar_hsa_circ_298677,RMVar_hsa_circ_219014,RMVar_hsa_circ_379023,RMVar_hsa_circ_302644,RMVar_hsa_circ_267678,RMVar_hsa_circ_269199,RMVar_hsa_circ_100147,RMVar_hsa_circ_6963,RMVar_hsa_circ_219015,RMVar_hsa_circ_219017,RMVar_hsa_circ_219018,RMVar_hsa_circ_219016,RMVar_hsa_circ_219022,RMVar_hsa_circ_83246,RMVar_hsa_circ_362275,RMVar_hsa_circ_91145,RMVar_hsa_circ_40140,RMVar_hsa_circ_219023,RMVar_hsa_circ_113851,RMVar_hsa_circ_268263,RMVar_hsa_circ_12624,RMVar_hsa_circ_37017,RMVar_hsa_circ_219024 29824 RMVar_ID_29824 Human_SNP_ID_134339856 A-to-I Human chr3 - 56630798 56630798 56630798 TCTTGTTGCCCAGGGTGGAGTGTAATGGCACTATCTTGGCTCACTGCAACCTCCGCCTTCTGGGG TCTTGTTGCCCAGGGTGGAGTGTAATGGCACTGTCTTGGCTCACTGCAACCTCCGCCTTCTGGGG T C TASOR Ensembl:ENSG00000163946 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs958725313 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5216,RMVar_hsa_circ_99242,RMVar_hsa_circ_268574,RMVar_hsa_circ_219010,RMVar_hsa_circ_219012,RMVar_hsa_circ_298677,RMVar_hsa_circ_219014,RMVar_hsa_circ_379023,RMVar_hsa_circ_302644,RMVar_hsa_circ_267678,RMVar_hsa_circ_269199,RMVar_hsa_circ_100147,RMVar_hsa_circ_6963,RMVar_hsa_circ_219015,RMVar_hsa_circ_219017,RMVar_hsa_circ_219018,RMVar_hsa_circ_219016,RMVar_hsa_circ_219022,RMVar_hsa_circ_83246,RMVar_hsa_circ_362275,RMVar_hsa_circ_91145,RMVar_hsa_circ_40140,RMVar_hsa_circ_219023,RMVar_hsa_circ_113851,RMVar_hsa_circ_268263,RMVar_hsa_circ_12624,RMVar_hsa_circ_37017,RMVar_hsa_circ_219024 29825 RMVar_ID_29825 Human_SNP_ID_134339857 A-to-I Human chr3 - 56630801 56630801 56630801 TGCTCTTGTTGCCCAGGGTGGAGTGTAATGGCACTATCTTGGCTCACTGCAACCTCCGCCTTCTG TGCTCTTGTTGCCCAGGGTGGAGTGTAATGGCGCTATCTTGGCTCACTGCAACCTCCGCCTTCTG T C TASOR Ensembl:ENSG00000163946 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1490184611 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5216,RMVar_hsa_circ_99242,RMVar_hsa_circ_268574,RMVar_hsa_circ_219010,RMVar_hsa_circ_219012,RMVar_hsa_circ_298677,RMVar_hsa_circ_219014,RMVar_hsa_circ_379023,RMVar_hsa_circ_302644,RMVar_hsa_circ_267678,RMVar_hsa_circ_269199,RMVar_hsa_circ_100147,RMVar_hsa_circ_6963,RMVar_hsa_circ_219015,RMVar_hsa_circ_219017,RMVar_hsa_circ_219018,RMVar_hsa_circ_219016,RMVar_hsa_circ_219022,RMVar_hsa_circ_83246,RMVar_hsa_circ_362275,RMVar_hsa_circ_91145,RMVar_hsa_circ_40140,RMVar_hsa_circ_219023,RMVar_hsa_circ_113851,RMVar_hsa_circ_268263,RMVar_hsa_circ_12624,RMVar_hsa_circ_37017,RMVar_hsa_circ_219024 29826 RMVar_ID_29826 Human_SNP_ID_134340167 A-to-I Human chr3 - 56631732 56631732 56631732 TAAAGTACAAAAAATTAGCCGGGCATGGGGGCAGGCGCCTGTAGTCCCAGCTACTCAGGAGGCTG TAAAGTACAAAAAATTAGCCGGGCATGGGGGCGGGCGCCTGTAGTCCCAGCTACTCAGGAGGCTG T C TASOR Ensembl:ENSG00000163946 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1384607944 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5216,RMVar_hsa_circ_99242,RMVar_hsa_circ_268574,RMVar_hsa_circ_219010,RMVar_hsa_circ_219012,RMVar_hsa_circ_298677,RMVar_hsa_circ_219014,RMVar_hsa_circ_379023,RMVar_hsa_circ_302644,RMVar_hsa_circ_267678,RMVar_hsa_circ_269199,RMVar_hsa_circ_100147,RMVar_hsa_circ_6963,RMVar_hsa_circ_219015,RMVar_hsa_circ_219017,RMVar_hsa_circ_219018,RMVar_hsa_circ_219016,RMVar_hsa_circ_219022,RMVar_hsa_circ_83246,RMVar_hsa_circ_362275,RMVar_hsa_circ_91145,RMVar_hsa_circ_40140,RMVar_hsa_circ_219023,RMVar_hsa_circ_113851,RMVar_hsa_circ_268263,RMVar_hsa_circ_12624,RMVar_hsa_circ_37017,RMVar_hsa_circ_219024 29827 RMVar_ID_29827 Human_SNP_ID_134340310 A-to-I Human chr3 - 56632238 56632238 56632238 TGGAACTCCTGGCCTCGTGATCCGTCCACCTCAGCCTCCCAAAGTGCTGAGATTACAGGCGTGGG TGGAACTCCTGGCCTCGTGATCCGTCCACCTCGGCCTCCCAAAGTGCTGAGATTACAGGCGTGGG T C TASOR Ensembl:ENSG00000163946 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1015081313 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5216,RMVar_hsa_circ_99242,RMVar_hsa_circ_268574,RMVar_hsa_circ_219010,RMVar_hsa_circ_219012,RMVar_hsa_circ_298677,RMVar_hsa_circ_219014,RMVar_hsa_circ_379023,RMVar_hsa_circ_302644,RMVar_hsa_circ_267678,RMVar_hsa_circ_269199,RMVar_hsa_circ_100147,RMVar_hsa_circ_6963,RMVar_hsa_circ_219015,RMVar_hsa_circ_219017,RMVar_hsa_circ_219018,RMVar_hsa_circ_219016,RMVar_hsa_circ_219022,RMVar_hsa_circ_83246,RMVar_hsa_circ_362275,RMVar_hsa_circ_91145,RMVar_hsa_circ_40140,RMVar_hsa_circ_219023,RMVar_hsa_circ_113851,RMVar_hsa_circ_268263,RMVar_hsa_circ_12624,RMVar_hsa_circ_37017,RMVar_hsa_circ_219024 29828 RMVar_ID_29828 Human_SNP_ID_134340332 A-to-I Human chr3 - 56632308 56632308 56632308 ACCATGCCTGGCTAATTTTTTTTTGTATTTTTAGTAGAGGTGGGGTTTCACCATGTTGATCAGGC ACCATGCCTGGCTAATTTTTTTTTGTATTTTTGGTAGAGGTGGGGTTTCACCATGTTGATCAGGC T C TASOR Ensembl:ENSG00000163946 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1224727353 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5216,RMVar_hsa_circ_99242,RMVar_hsa_circ_268574,RMVar_hsa_circ_219010,RMVar_hsa_circ_219012,RMVar_hsa_circ_298677,RMVar_hsa_circ_219014,RMVar_hsa_circ_379023,RMVar_hsa_circ_302644,RMVar_hsa_circ_267678,RMVar_hsa_circ_269199,RMVar_hsa_circ_100147,RMVar_hsa_circ_6963,RMVar_hsa_circ_219015,RMVar_hsa_circ_219017,RMVar_hsa_circ_219018,RMVar_hsa_circ_219016,RMVar_hsa_circ_219022,RMVar_hsa_circ_83246,RMVar_hsa_circ_362275,RMVar_hsa_circ_91145,RMVar_hsa_circ_40140,RMVar_hsa_circ_219023,RMVar_hsa_circ_113851,RMVar_hsa_circ_268263,RMVar_hsa_circ_12624,RMVar_hsa_circ_37017,RMVar_hsa_circ_219024 29829 RMVar_ID_29829 Human_SNP_ID_134340445 A-to-I Human chr3 - 56632909 56632876 56632910 TGTTAGGCCAGGAATGGTGGCTAATACCTGTAATCCCAAAACTTGGGAGGCTGAGGCAGGAGGAT TGTTAGGCCAGGAATGGTGGCTAATACCTGT__________________________________ AATCCTCCTGCCTCAGCCTCCCAAGTTTTGGGATT A TASOR Ensembl:ENSG00000163946 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1430405595 Functional Loss DEL dbSNP153 32..65 33 - - - RMVar_hsa_circ_5216,RMVar_hsa_circ_99242,RMVar_hsa_circ_268574,RMVar_hsa_circ_219010,RMVar_hsa_circ_219012,RMVar_hsa_circ_298677,RMVar_hsa_circ_219014,RMVar_hsa_circ_379023,RMVar_hsa_circ_302644,RMVar_hsa_circ_267678,RMVar_hsa_circ_269199,RMVar_hsa_circ_100147,RMVar_hsa_circ_6963,RMVar_hsa_circ_219015,RMVar_hsa_circ_219017,RMVar_hsa_circ_219018,RMVar_hsa_circ_219016,RMVar_hsa_circ_219022,RMVar_hsa_circ_83246,RMVar_hsa_circ_362275,RMVar_hsa_circ_91145,RMVar_hsa_circ_40140,RMVar_hsa_circ_219023,RMVar_hsa_circ_113851,RMVar_hsa_circ_268263,RMVar_hsa_circ_12624,RMVar_hsa_circ_37017,RMVar_hsa_circ_219024 29830 RMVar_ID_29830 Human_SNP_ID_134340445 A-to-I Human chr3 - 56632910 56632876 56632910 ATGTTAGGCCAGGAATGGTGGCTAATACCTGTAATCCCAAAACTTGGGAGGCTGAGGCAGGAGGA ATGTTAGGCCAGGAATGGTGGCTAATACCTGT_________________________________ AATCCTCCTGCCTCAGCCTCCCAAGTTTTGGGATT A TASOR Ensembl:ENSG00000163946 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1430405595 Functional Loss DEL dbSNP153 33..65 33 - - - RMVar_hsa_circ_5216,RMVar_hsa_circ_99242,RMVar_hsa_circ_268574,RMVar_hsa_circ_219010,RMVar_hsa_circ_219012,RMVar_hsa_circ_298677,RMVar_hsa_circ_219014,RMVar_hsa_circ_379023,RMVar_hsa_circ_302644,RMVar_hsa_circ_267678,RMVar_hsa_circ_269199,RMVar_hsa_circ_100147,RMVar_hsa_circ_6963,RMVar_hsa_circ_219015,RMVar_hsa_circ_219017,RMVar_hsa_circ_219018,RMVar_hsa_circ_219016,RMVar_hsa_circ_219022,RMVar_hsa_circ_83246,RMVar_hsa_circ_362275,RMVar_hsa_circ_91145,RMVar_hsa_circ_40140,RMVar_hsa_circ_219023,RMVar_hsa_circ_113851,RMVar_hsa_circ_268263,RMVar_hsa_circ_12624,RMVar_hsa_circ_37017,RMVar_hsa_circ_219024 29831 RMVar_ID_29831 Human_SNP_ID_134340446 A-to-I Human chr3 - 56632884 56632884 56632884 ACCTGTAATCCCAAAACTTGGGAGGCTGAGGCAGGAGGATTGCTTGAGGCCAGGAGTTCATGACA ACCTGTAATCCCAAAACTTGGGAGGCTGAGGCTGGAGGATTGCTTGAGGCCAGGAGTTCATGACA T A TASOR Ensembl:ENSG00000163946 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1193227833 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25747634 RMVar_hsa_circ_5216,RMVar_hsa_circ_99242,RMVar_hsa_circ_268574,RMVar_hsa_circ_219010,RMVar_hsa_circ_219012,RMVar_hsa_circ_298677,RMVar_hsa_circ_219014,RMVar_hsa_circ_379023,RMVar_hsa_circ_302644,RMVar_hsa_circ_267678,RMVar_hsa_circ_269199,RMVar_hsa_circ_100147,RMVar_hsa_circ_6963,RMVar_hsa_circ_219015,RMVar_hsa_circ_219017,RMVar_hsa_circ_219018,RMVar_hsa_circ_219016,RMVar_hsa_circ_219022,RMVar_hsa_circ_83246,RMVar_hsa_circ_362275,RMVar_hsa_circ_91145,RMVar_hsa_circ_40140,RMVar_hsa_circ_219023,RMVar_hsa_circ_113851,RMVar_hsa_circ_268263,RMVar_hsa_circ_12624,RMVar_hsa_circ_37017,RMVar_hsa_circ_219024 29832 RMVar_ID_29832 Human_SNP_ID_134345473 A-to-I Human chr3 - 56652113 56652113 56652113 CTTCTGTCTCTATGGATTTATCTGCTCTGAACATTTTATATAAATAGAGTCAAGAATATGTGGCG CTTCTGTCTCTATGGATTTATCTGCTCTGAACGTTTTATATAAATAGAGTCAAGAATATGTGGCG T C TASOR Ensembl:ENSG00000163946 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027200973 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14906151,Human_RBP_ID_20929463 RMVar_hsa_circ_99242,RMVar_hsa_circ_268574,RMVar_hsa_circ_219010,RMVar_hsa_circ_219012,RMVar_hsa_circ_219014,RMVar_hsa_circ_302644,RMVar_hsa_circ_269199,RMVar_hsa_circ_100147,RMVar_hsa_circ_13809,RMVar_hsa_circ_29175,RMVar_hsa_circ_219015,RMVar_hsa_circ_219016,RMVar_hsa_circ_219022,RMVar_hsa_circ_83246,RMVar_hsa_circ_91145,RMVar_hsa_circ_219023,RMVar_hsa_circ_113851,RMVar_hsa_circ_268263,RMVar_hsa_circ_37017,RMVar_hsa_circ_219024,RMVar_hsa_circ_335873,RMVar_hsa_circ_306422,RMVar_hsa_circ_289359,RMVar_hsa_circ_59876,RMVar_hsa_circ_219030,RMVar_hsa_circ_32577,RMVar_hsa_circ_219029,RMVar_hsa_circ_277304,RMVar_hsa_circ_2152,RMVar_hsa_circ_13924,RMVar_hsa_circ_82990,RMVar_hsa_circ_219031,RMVar_hsa_circ_281690,RMVar_hsa_circ_219034,RMVar_hsa_circ_219035,RMVar_hsa_circ_331202,RMVar_hsa_circ_21377,RMVar_hsa_circ_105759,RMVar_hsa_circ_17453,RMVar_hsa_circ_17089,RMVar_hsa_circ_219037,RMVar_hsa_circ_219038,RMVar_hsa_circ_272916,RMVar_hsa_circ_325790,RMVar_hsa_circ_283778,RMVar_hsa_circ_27825,RMVar_hsa_circ_93166,RMVar_hsa_circ_219040,RMVar_hsa_circ_219041,RMVar_hsa_circ_219039,RMVar_hsa_circ_61994,RMVar_hsa_circ_219043,RMVar_hsa_circ_219044 29833 RMVar_ID_29833 Human_SNP_ID_134347597 A-to-I Human chr3 - 56659942 56659942 56659942 TGAACCCAGGAGGAAGAGGTTGTGGTGAGCCAAGATCGTACCATTGCGCTCCAGCCTGAGTGACA TGAACCCAGGAGGAAGAGGTTGTGGTGAGCCAGGATCGTACCATTGCGCTCCAGCCTGAGTGACA T C TASOR Ensembl:ENSG00000163946 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1298250077 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99242,RMVar_hsa_circ_268574,RMVar_hsa_circ_219010,RMVar_hsa_circ_219012,RMVar_hsa_circ_219014,RMVar_hsa_circ_302644,RMVar_hsa_circ_269199,RMVar_hsa_circ_100147,RMVar_hsa_circ_13809,RMVar_hsa_circ_29175,RMVar_hsa_circ_219015,RMVar_hsa_circ_219016,RMVar_hsa_circ_219022,RMVar_hsa_circ_83246,RMVar_hsa_circ_91145,RMVar_hsa_circ_219023,RMVar_hsa_circ_113851,RMVar_hsa_circ_268263,RMVar_hsa_circ_37017,RMVar_hsa_circ_219024,RMVar_hsa_circ_335873,RMVar_hsa_circ_306422,RMVar_hsa_circ_289359,RMVar_hsa_circ_59876,RMVar_hsa_circ_219030,RMVar_hsa_circ_32577,RMVar_hsa_circ_219029,RMVar_hsa_circ_277304,RMVar_hsa_circ_2152,RMVar_hsa_circ_13924,RMVar_hsa_circ_82990,RMVar_hsa_circ_219031,RMVar_hsa_circ_281690,RMVar_hsa_circ_219034,RMVar_hsa_circ_219035,RMVar_hsa_circ_331202,RMVar_hsa_circ_21377,RMVar_hsa_circ_105759,RMVar_hsa_circ_17453,RMVar_hsa_circ_17089,RMVar_hsa_circ_219037,RMVar_hsa_circ_219038,RMVar_hsa_circ_272916,RMVar_hsa_circ_325790,RMVar_hsa_circ_283778,RMVar_hsa_circ_27825,RMVar_hsa_circ_93166,RMVar_hsa_circ_219040,RMVar_hsa_circ_219041,RMVar_hsa_circ_219039,RMVar_hsa_circ_61994,RMVar_hsa_circ_219043,RMVar_hsa_circ_219044 29834 RMVar_ID_29834 Human_SNP_ID_134348124 A-to-I Human chr3 - 56661906 56661906 56661906 CAGTCAGTCTGGTCTCGAACTCCTGACCTCATATGATCCTCCCGCCTTGGCCTCACGAAGTGTTG CAGTCAGTCTGGTCTCGAACTCCTGACCTCATGTGATCCTCCCGCCTTGGCCTCACGAAGTGTTG T C TASOR Ensembl:ENSG00000163946 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1179406530 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14906522,Human_RBP_ID_25771486 RMVar_hsa_circ_268574,RMVar_hsa_circ_219012,RMVar_hsa_circ_219014,RMVar_hsa_circ_302644,RMVar_hsa_circ_269199,RMVar_hsa_circ_13809,RMVar_hsa_circ_29175,RMVar_hsa_circ_219015,RMVar_hsa_circ_91145,RMVar_hsa_circ_219023,RMVar_hsa_circ_113851,RMVar_hsa_circ_268263,RMVar_hsa_circ_37017,RMVar_hsa_circ_219024,RMVar_hsa_circ_306422,RMVar_hsa_circ_289359,RMVar_hsa_circ_59876,RMVar_hsa_circ_219030,RMVar_hsa_circ_32577,RMVar_hsa_circ_277304,RMVar_hsa_circ_13924,RMVar_hsa_circ_219031,RMVar_hsa_circ_281690,RMVar_hsa_circ_219035,RMVar_hsa_circ_331202,RMVar_hsa_circ_21377,RMVar_hsa_circ_105759,RMVar_hsa_circ_17453,RMVar_hsa_circ_17089,RMVar_hsa_circ_219037,RMVar_hsa_circ_219038,RMVar_hsa_circ_272916,RMVar_hsa_circ_27825,RMVar_hsa_circ_93166,RMVar_hsa_circ_219040,RMVar_hsa_circ_219039,RMVar_hsa_circ_61994,RMVar_hsa_circ_33467,RMVar_hsa_circ_219047,RMVar_hsa_circ_285357,RMVar_hsa_circ_219043,RMVar_hsa_circ_219044,RMVar_hsa_circ_339428,RMVar_hsa_circ_354909,RMVar_hsa_circ_361332,RMVar_hsa_circ_339472,RMVar_hsa_circ_309761,RMVar_hsa_circ_123295,RMVar_hsa_circ_219048,RMVar_hsa_circ_219049,RMVar_hsa_circ_219046,RMVar_hsa_circ_98081,RMVar_hsa_circ_219050 29835 RMVar_ID_29835 Human_SNP_ID_134348930 A-to-I Human chr3 - 56665159 56665159 56665159 ACCCTCTGTTTCTTTTTTTTTCCTCTTTAGAGACAAAGTCTTGCTCTGTTGCCCAGGCTGTAGTG ACCCTCTGTTTCTTTTTTTTTCCTCTTTAGAGTCAAAGTCTTGCTCTGTTGCCCAGGCTGTAGTG T A TASOR Ensembl:ENSG00000163946 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1414674124 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7213710,Human_RBP_ID_14906673 RMVar_hsa_circ_268574,RMVar_hsa_circ_219012,RMVar_hsa_circ_219014,RMVar_hsa_circ_302644,RMVar_hsa_circ_269199,RMVar_hsa_circ_13809,RMVar_hsa_circ_219015,RMVar_hsa_circ_113851,RMVar_hsa_circ_268263,RMVar_hsa_circ_37017,RMVar_hsa_circ_219024,RMVar_hsa_circ_306422,RMVar_hsa_circ_59876,RMVar_hsa_circ_32577,RMVar_hsa_circ_277304,RMVar_hsa_circ_13924,RMVar_hsa_circ_219031,RMVar_hsa_circ_281690,RMVar_hsa_circ_219035,RMVar_hsa_circ_331202,RMVar_hsa_circ_105759,RMVar_hsa_circ_17453,RMVar_hsa_circ_219037,RMVar_hsa_circ_219038,RMVar_hsa_circ_272916,RMVar_hsa_circ_27825,RMVar_hsa_circ_93166,RMVar_hsa_circ_219039,RMVar_hsa_circ_219047,RMVar_hsa_circ_285357,RMVar_hsa_circ_219043,RMVar_hsa_circ_219044,RMVar_hsa_circ_354909,RMVar_hsa_circ_361332,RMVar_hsa_circ_339472,RMVar_hsa_circ_309761,RMVar_hsa_circ_123295,RMVar_hsa_circ_219048,RMVar_hsa_circ_219049,RMVar_hsa_circ_219046,RMVar_hsa_circ_98081,RMVar_hsa_circ_81543,RMVar_hsa_circ_219051,RMVar_hsa_circ_219050,RMVar_hsa_circ_303902,RMVar_hsa_circ_268625,RMVar_hsa_circ_308400,RMVar_hsa_circ_112093,RMVar_hsa_circ_219053,RMVar_hsa_circ_219054,RMVar_hsa_circ_219052 29836 RMVar_ID_29836 Human_SNP_ID_134349073 A-to-I Human chr3 - 56665648 56665648 56665648 CAGTTTTAAAAAGTGAGATTTTGGCCAGGCGCAGTGGCTCATGCCTGTAATTCCAGCACTTTGGG CAGTTTTAAAAAGTGAGATTTTGGCCAGGCGCGGTGGCTCATGCCTGTAATTCCAGCACTTTGGG T C TASOR Ensembl:ENSG00000163946 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs544974680 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268574,RMVar_hsa_circ_219012,RMVar_hsa_circ_219014,RMVar_hsa_circ_302644,RMVar_hsa_circ_269199,RMVar_hsa_circ_13809,RMVar_hsa_circ_219015,RMVar_hsa_circ_113851,RMVar_hsa_circ_268263,RMVar_hsa_circ_37017,RMVar_hsa_circ_219024,RMVar_hsa_circ_306422,RMVar_hsa_circ_59876,RMVar_hsa_circ_32577,RMVar_hsa_circ_277304,RMVar_hsa_circ_13924,RMVar_hsa_circ_219031,RMVar_hsa_circ_281690,RMVar_hsa_circ_219035,RMVar_hsa_circ_331202,RMVar_hsa_circ_105759,RMVar_hsa_circ_17453,RMVar_hsa_circ_219037,RMVar_hsa_circ_219038,RMVar_hsa_circ_272916,RMVar_hsa_circ_27825,RMVar_hsa_circ_93166,RMVar_hsa_circ_219039,RMVar_hsa_circ_219047,RMVar_hsa_circ_285357,RMVar_hsa_circ_219043,RMVar_hsa_circ_219044,RMVar_hsa_circ_354909,RMVar_hsa_circ_361332,RMVar_hsa_circ_339472,RMVar_hsa_circ_309761,RMVar_hsa_circ_123295,RMVar_hsa_circ_219048,RMVar_hsa_circ_219049,RMVar_hsa_circ_219046,RMVar_hsa_circ_98081,RMVar_hsa_circ_81543,RMVar_hsa_circ_219051,RMVar_hsa_circ_219050,RMVar_hsa_circ_303902,RMVar_hsa_circ_268625,RMVar_hsa_circ_308400,RMVar_hsa_circ_112093,RMVar_hsa_circ_219053,RMVar_hsa_circ_219054,RMVar_hsa_circ_219052 29837 RMVar_ID_29837 Human_SNP_ID_134349074 A-to-I Human chr3 - 56665648 56665648 56665648 CAGTTTTAAAAAGTGAGATTTTGGCCAGGCGCAGTGGCTCATGCCTGTAATTCCAGCACTTTGGG CAGTTTTAAAAAGTGAGATTTTGGCCAGGCGCCGTGGCTCATGCCTGTAATTCCAGCACTTTGGG T G TASOR Ensembl:ENSG00000163946 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs544974680 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268574,RMVar_hsa_circ_219012,RMVar_hsa_circ_219014,RMVar_hsa_circ_302644,RMVar_hsa_circ_269199,RMVar_hsa_circ_13809,RMVar_hsa_circ_219015,RMVar_hsa_circ_113851,RMVar_hsa_circ_268263,RMVar_hsa_circ_37017,RMVar_hsa_circ_219024,RMVar_hsa_circ_306422,RMVar_hsa_circ_59876,RMVar_hsa_circ_32577,RMVar_hsa_circ_277304,RMVar_hsa_circ_13924,RMVar_hsa_circ_219031,RMVar_hsa_circ_281690,RMVar_hsa_circ_219035,RMVar_hsa_circ_331202,RMVar_hsa_circ_105759,RMVar_hsa_circ_17453,RMVar_hsa_circ_219037,RMVar_hsa_circ_219038,RMVar_hsa_circ_272916,RMVar_hsa_circ_27825,RMVar_hsa_circ_93166,RMVar_hsa_circ_219039,RMVar_hsa_circ_219047,RMVar_hsa_circ_285357,RMVar_hsa_circ_219043,RMVar_hsa_circ_219044,RMVar_hsa_circ_354909,RMVar_hsa_circ_361332,RMVar_hsa_circ_339472,RMVar_hsa_circ_309761,RMVar_hsa_circ_123295,RMVar_hsa_circ_219048,RMVar_hsa_circ_219049,RMVar_hsa_circ_219046,RMVar_hsa_circ_98081,RMVar_hsa_circ_81543,RMVar_hsa_circ_219051,RMVar_hsa_circ_219050,RMVar_hsa_circ_303902,RMVar_hsa_circ_268625,RMVar_hsa_circ_308400,RMVar_hsa_circ_112093,RMVar_hsa_circ_219053,RMVar_hsa_circ_219054,RMVar_hsa_circ_219052 29838 RMVar_ID_29838 Human_SNP_ID_134349138 A-to-I Human chr3 - 56665850 56665850 56665850 ATTCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCACATACCACCATGCCTGGCTAATTTTT ATTCTGCCTCAGCCTCCCGAGTAGCTGGGACTGCAGGCACATACCACCATGCCTGGCTAATTTTT T C TASOR Ensembl:ENSG00000163946 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1282192575 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268574,RMVar_hsa_circ_219012,RMVar_hsa_circ_219014,RMVar_hsa_circ_302644,RMVar_hsa_circ_269199,RMVar_hsa_circ_13809,RMVar_hsa_circ_219015,RMVar_hsa_circ_113851,RMVar_hsa_circ_268263,RMVar_hsa_circ_37017,RMVar_hsa_circ_219024,RMVar_hsa_circ_306422,RMVar_hsa_circ_59876,RMVar_hsa_circ_32577,RMVar_hsa_circ_277304,RMVar_hsa_circ_13924,RMVar_hsa_circ_219031,RMVar_hsa_circ_281690,RMVar_hsa_circ_219035,RMVar_hsa_circ_331202,RMVar_hsa_circ_105759,RMVar_hsa_circ_17453,RMVar_hsa_circ_219037,RMVar_hsa_circ_219038,RMVar_hsa_circ_272916,RMVar_hsa_circ_27825,RMVar_hsa_circ_93166,RMVar_hsa_circ_219039,RMVar_hsa_circ_219047,RMVar_hsa_circ_285357,RMVar_hsa_circ_219043,RMVar_hsa_circ_219044,RMVar_hsa_circ_354909,RMVar_hsa_circ_361332,RMVar_hsa_circ_339472,RMVar_hsa_circ_309761,RMVar_hsa_circ_123295,RMVar_hsa_circ_219048,RMVar_hsa_circ_219049,RMVar_hsa_circ_219046,RMVar_hsa_circ_98081,RMVar_hsa_circ_81543,RMVar_hsa_circ_219051,RMVar_hsa_circ_219050,RMVar_hsa_circ_303902,RMVar_hsa_circ_268625,RMVar_hsa_circ_308400,RMVar_hsa_circ_112093,RMVar_hsa_circ_219053,RMVar_hsa_circ_219054,RMVar_hsa_circ_219052 29839 RMVar_ID_29839 Human_SNP_ID_134349158 A-to-I Human chr3 - 56665906 56665906 56665906 GGAGTGCATTGGCAGGATCTCGGCTCACTGCAAGCTCCGCCTCCCGGGTTCACGCCATTCTGCCT GGAGTGCATTGGCAGGATCTCGGCTCACTGCAGGCTCCGCCTCCCGGGTTCACGCCATTCTGCCT T C TASOR Ensembl:ENSG00000163946 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1011320607 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14906697 RMVar_hsa_circ_268574,RMVar_hsa_circ_219012,RMVar_hsa_circ_219014,RMVar_hsa_circ_302644,RMVar_hsa_circ_269199,RMVar_hsa_circ_13809,RMVar_hsa_circ_219015,RMVar_hsa_circ_113851,RMVar_hsa_circ_268263,RMVar_hsa_circ_37017,RMVar_hsa_circ_219024,RMVar_hsa_circ_306422,RMVar_hsa_circ_59876,RMVar_hsa_circ_32577,RMVar_hsa_circ_277304,RMVar_hsa_circ_13924,RMVar_hsa_circ_219031,RMVar_hsa_circ_281690,RMVar_hsa_circ_219035,RMVar_hsa_circ_331202,RMVar_hsa_circ_105759,RMVar_hsa_circ_17453,RMVar_hsa_circ_219037,RMVar_hsa_circ_219038,RMVar_hsa_circ_272916,RMVar_hsa_circ_27825,RMVar_hsa_circ_93166,RMVar_hsa_circ_219039,RMVar_hsa_circ_219047,RMVar_hsa_circ_285357,RMVar_hsa_circ_219043,RMVar_hsa_circ_219044,RMVar_hsa_circ_354909,RMVar_hsa_circ_361332,RMVar_hsa_circ_339472,RMVar_hsa_circ_309761,RMVar_hsa_circ_123295,RMVar_hsa_circ_219048,RMVar_hsa_circ_219049,RMVar_hsa_circ_219046,RMVar_hsa_circ_98081,RMVar_hsa_circ_81543,RMVar_hsa_circ_219051,RMVar_hsa_circ_219050,RMVar_hsa_circ_303902,RMVar_hsa_circ_268625,RMVar_hsa_circ_308400,RMVar_hsa_circ_112093,RMVar_hsa_circ_219053,RMVar_hsa_circ_219054,RMVar_hsa_circ_219052 29840 RMVar_ID_29840 Human_SNP_ID_134351513 A-to-I Human chr3 - 56674503 56674501 56674503 AGCATTTTATTTTTTATTTTTATTTTTGAGACAGGGTCTCTCTCTCACTCCCAGACTGGAGTGCG AGCATTTTATTTTTTATTTTTATTTTTGAGAC__GGTCTCTCTCTCACTCCCAGACTGGAGTGCG CCT C TASOR Ensembl:ENSG00000163946 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1256133913 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_26685871 RMVar_hsa_circ_120967,RMVar_hsa_circ_219059 29841 RMVar_ID_29841 Human_SNP_ID_134351515 A-to-I Human chr3 - 56674503 56674503 56674503 AGCATTTTATTTTTTATTTTTATTTTTGAGACAGGGTCTCTCTCTCACTCCCAGACTGGAGTGCG AGCATTTTATTTTTTATTTTTATTTTTGAGACGGGGTCTCTCTCTCACTCCCAGACTGGAGTGCG T C TASOR Ensembl:ENSG00000163946 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs761308832 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26685871 RMVar_hsa_circ_120967,RMVar_hsa_circ_219059 29842 RMVar_ID_29842 Human_SNP_ID_134351643 A-to-I Human chr3 - 56674947 56674947 56674947 GGGTGTGGTGGTGGGTGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATGGTGTGTA GGGTGTGGTGGTGGGTGCCTGTAGTCCCAGCTGCTTGGGAGGCTGAGGCAGGAGAATGGTGTGTA T C TASOR Ensembl:ENSG00000163946 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs568187627 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120967,RMVar_hsa_circ_219059 29843 RMVar_ID_29843 Human_SNP_ID_134352608 A-to-I Human chr3 - 56678274 56678274 56678274 GGGAGGCTGAGGCAGGAGAATAGCTTGAACCCAGGAGGTGGAAGTTGCAGTGAGCCAAGATCGCG GGGAGGCTGAGGCAGGAGAATAGCTTGAACCCCGGAGGTGGAAGTTGCAGTGAGCCAAGATCGCG T G TASOR Ensembl:ENSG00000163946 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs375061628 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120967,RMVar_hsa_circ_219059 29844 RMVar_ID_29844 Human_SNP_ID_134352729 A-to-I Human chr3 - 56678754 56678754 56678754 CGCCCTCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCGCCACGCCCAGCCCCATTTG CGCCCTCCTTGGCCTCCCAAAGTGCTGGGATTGCAGGCATGAGCCGCCACGCCCAGCCCCATTTG T C TASOR Ensembl:ENSG00000163946 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1460276025 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120967,RMVar_hsa_circ_219059 29845 RMVar_ID_29845 Human_SNP_ID_134352733 A-to-I Human chr3 - 56678767 56678767 56678767 ACCTGAAGTGATCCGCCCTCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCGCCACGC ACCTGAAGTGATCCGCCCTCCTTGGCCTCCCAGAGTGCTGGGATTACAGGCATGAGCCGCCACGC T C TASOR Ensembl:ENSG00000163946 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs544321996 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120967,RMVar_hsa_circ_219059 29846 RMVar_ID_29846 Human_SNP_ID_134352763 A-to-I Human chr3 - 56678889 56678889 56678889 TCCTTCCTTAGCCTCCCCCAGTAGTTCGGATTACAGGCATGTGCCACCACGCCCAGCTAATTTTT TCCTTCCTTAGCCTCCCCCAGTAGTTCGGATTGCAGGCATGTGCCACCACGCCCAGCTAATTTTT T C TASOR Ensembl:ENSG00000163946 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1439411810 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120967,RMVar_hsa_circ_219059 29847 RMVar_ID_29847 Human_SNP_ID_134367460 A-to-I Human chr3 - 56731546 56731546 56731546 AGGGATAGCAATAGGAGGTCTGTTTTATTTTTATTTATTTATTTTTTTGAGACAGAGTCTTCCTC AGGGATAGCAATAGGAGGTCTGTTTTATTTTTTTTTATTTATTTTTTTGAGACAGAGTCTTCCTC T A ARHGEF3 Ensembl:ENSG00000163947 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053017398 Functional Loss SNV dbSNP153 33..33 33 - - - 29848 RMVar_ID_29848 Human_SNP_ID_134369612 A-to-I Human chr3 - 56739564 56739564 56739564 AAAAACCCATCTCCATGAAAAATACAAAAATTAGCCAGGTGTGGTGGCGCACGCCTGTGGTCCCA AAAAACCCATCTCCATGAAAAATACAAAAATTGGCCAGGTGTGGTGGCGCACGCCTGTGGTCCCA T C ARHGEF3 Ensembl:ENSG00000163947 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs969054517 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29507,RMVar_hsa_circ_377252,RMVar_hsa_circ_39592,RMVar_hsa_circ_283366,RMVar_hsa_circ_219065 29849 RMVar_ID_29849 Human_SNP_ID_134391836 A-to-I Human chr3 - 56836691 56836691 56836691 AAATTCCTGGGCTCAAACGATCCTCCTACCTCAGCCTCCCAAAGTGCTGGGACTACAGGCGTAAG AAATTCCTGGGCTCAAACGATCCTCCTACCTCCGCCTCCCAAAGTGCTGGGACTACAGGCGTAAG T G ARHGEF3 Ensembl:ENSG00000163947 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1269777442 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17525,RMVar_hsa_circ_308921 29850 RMVar_ID_29850 Human_SNP_ID_134454168 A-to-I Human chr3 - 57090543 57090543 57090543 AAATTAATCAGGCGTGGTTGTGTGTGCCTGTAATCCCAGCTACTCGAGAGGCTGAGGCAGGAGAA AAATTAATCAGGCGTGGTTGTGTGTGCCTGTAGTCCCAGCTACTCGAGAGGCTGAGGCAGGAGAA T C IL17RD Ensembl:ENSG00000144730 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1360132105 Functional Loss SNV dbSNP153 33..33 33 - - - 29851 RMVar_ID_29851 Human_SNP_ID_134454169 A-to-I Human chr3 - 57090544 57090544 57090544 AAAATTAATCAGGCGTGGTTGTGTGTGCCTGTAATCCCAGCTACTCGAGAGGCTGAGGCAGGAGA AAAATTAATCAGGCGTGGTTGTGTGTGCCTGTGATCCCAGCTACTCGAGAGGCTGAGGCAGGAGA T C IL17RD Ensembl:ENSG00000144730 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1339059703 Functional Loss SNV dbSNP153 33..33 33 - - - 29852 RMVar_ID_29852 Human_SNP_ID_134454183 A-to-I Human chr3 - 57090609 57090609 57090609 CCTGAGGTCCAGAGTTCAAGACCAGCCTGACCAACATGGTGAAACCCTGTCTCTACTAAAAATAC CCTGAGGTCCAGAGTTCAAGACCAGCCTGACCGACATGGTGAAACCCTGTCTCTACTAAAAATAC T C IL17RD Ensembl:ENSG00000144730 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1268681767 Functional Loss SNV dbSNP153 33..33 33 - - - 29853 RMVar_ID_29853 Human_SNP_ID_134488129 A-to-I Human chr3 + 57230946 57230946 57230946 GGAGATGGAGTTTCGCTCTTGTCGCCTAGGCTAGAGTGCAGTGGCATGATCTTGGCTCACTGCAA GGAGATGGAGTTTCGCTCTTGTCGCCTAGGCTGGAGTGCAGTGGCATGATCTTGGCTCACTGCAA A G APPL1 Ensembl:ENSG00000157500 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232660013 Functional Loss SNV dbSNP153 33..33 33 - - - 29854 RMVar_ID_29854 Human_SNP_ID_134572834 A-to-I Human chr3 + 57563249 57563249 57563249 GCTGGAGTGCAGTGGTGCAGTCATAACTTACTACAGCCTCAAACTGCGGGGCTCAAATGATCCTC GCTGGAGTGCAGTGGTGCAGTCATAACTTACTGCAGCCTCAAACTGCGGGGCTCAAATGATCCTC A G PDE12 Ensembl:ENSG00000174840 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1411992588 Functional Loss SNV dbSNP153 33..33 33 - - - 29855 RMVar_ID_29855 Human_SNP_ID_134572847 A-to-I Human chr3 + 57563297 57563297 57563297 GGGCTCAAATGATCCTCCTGCCTCAGCGTCCCAAGTAGTTGAGATTACAAGCCCAACCTTCCATA GGGCTCAAATGATCCTCCTGCCTCAGCGTCCCGAGTAGTTGAGATTACAAGCCCAACCTTCCATA A G PDE12 Ensembl:ENSG00000174840 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs532508366 Functional Loss SNV dbSNP153 33..33 33 - - - 29856 RMVar_ID_29856 Human_SNP_ID_134572848 A-to-I Human chr3 + 57563297 57563297 57563297 GGGCTCAAATGATCCTCCTGCCTCAGCGTCCCAAGTAGTTGAGATTACAAGCCCAACCTTCCATA GGGCTCAAATGATCCTCCTGCCTCAGCGTCCCTAGTAGTTGAGATTACAAGCCCAACCTTCCATA A T PDE12 Ensembl:ENSG00000174840 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs532508366 Functional Loss SNV dbSNP153 33..33 33 - - - 29857 RMVar_ID_29857 Human_SNP_ID_134572929 A-to-I Human chr3 + 57563637 57563634 57563637 GGCCAGGCATAGTGGCTCTTGACTGTAATCACAACATTTTGGGAGGCTGAGGCAGGAGGATCACT GGCCAGGCATAGTGGCTCTTGACTGTAATC___ACATTTTGGGAGGCTGAGGCAGGAGGATCACT CACA C PDE12 Ensembl:ENSG00000174840 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1417296535 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_1966620 29858 RMVar_ID_29858 Human_SNP_ID_134573016 A-to-I Human chr3 + 57564109 57564109 57564109 CATACAGTACTGCTTGTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATATTGGCCAGGC CATACAGTACTGCTTGTAATTTTTGTATTTTTGGTAGAGACAGGGTTTCACCATATTGGCCAGGC A G PDE12 Ensembl:ENSG00000174840 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1187142967 Functional Loss SNV dbSNP153 33..33 33 - - - 29859 RMVar_ID_29859 Human_SNP_ID_134573375 A-to-I Human chr3 - 57565572 57565572 57565572 GTCTCGATCTGACCTCATGATCCACCGGCCTCAGCCTCCCAGAGTGCTGGGATTACAGGCGTGAG GTCTCGATCTGACCTCATGATCCACCGGCCTCGGCCTCCCAGAGTGCTGGGATTACAGGCGTGAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1559779612 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2793918 29860 RMVar_ID_29860 Human_SNP_ID_134574278 A-to-I Human chr3 + 57569590 57569590 57569590 GTTAGTCAGTCTGGTCTTGAACTCCCAACCTCAGGTGATCCACCTGCCTCGGCCTCCCAAAGTGC GTTAGTCAGTCTGGTCTTGAACTCCCAACCTCGGGTGATCCACCTGCCTCGGCCTCCCAAAGTGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1339145791 Functional Loss SNV dbSNP153 33..33 33 - - - 29861 RMVar_ID_29861 Human_SNP_ID_134574774 A-to-I Human chr3 + 57571111 57571111 57571111 GTGACCCTCCTGCCTCAACCTCCTAAAGTGCTAGGATTACAGGCGTGAGCCACCATGCCAGGCCC GTGACCCTCCTGCCTCAACCTCCTAAAGTGCTGGGATTACAGGCGTGAGCCACCATGCCAGGCCC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1345592904 Functional Loss SNV dbSNP153 33..33 33 - - - 29862 RMVar_ID_29862 Human_SNP_ID_134574912 A-to-I Human chr3 - 57571717 57571717 57571717 GAAAGATCCAAAACACTACTCAGCTCTCTTGCACTGAGGAAATTTTTCCCCCTACATTGACTCCT GAAAGATCCAAAACACTACTCAGCTCTCTTGCGCTGAGGAAATTTTTCCCCCTACATTGACTCCT T C ARF4 Ensembl:ENSG00000168374 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs149547076 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_606737,Human_RBP_ID_1966627,Human_RBP_ID_8209759,Human_RBP_ID_9142487,Human_RBP_ID_14908701,Human_RBP_ID_18340176,Human_RBP_ID_24428464,Human_RBP_ID_24498782,Human_RBP_ID_26510457 Human_miRNA_ID_213530,Human_miRNA_ID_223064,Human_miRNA_ID_328617,Human_miRNA_ID_332639,Human_miRNA_ID_349704,Human_miRNA_ID_517519,Human_miRNA_ID_521748,Human_miRNA_ID_761580,Human_miRNA_ID_766492,Human_miRNA_ID_1326076,Human_miRNA_ID_2018833,Human_miRNA_ID_2023926,Human_miRNA_ID_2077916,Human_miRNA_ID_2080244,Human_miRNA_ID_2090780,Human_miRNA_ID_2310549,Human_miRNA_ID_2312569,Human_miRNA_ID_2498658,Human_miRNA_ID_2606441,Human_miRNA_ID_2654347,Human_miRNA_ID_2945055,Human_miRNA_ID_2997716 RMVar_hsa_circ_106465,RMVar_hsa_circ_123839,RMVar_hsa_circ_127739,RMVar_hsa_circ_219100,RMVar_hsa_circ_219102,RMVar_hsa_circ_92045,RMVar_hsa_circ_219101,RMVar_hsa_circ_219099 29863 RMVar_ID_29863 Human_SNP_ID_134575406 A-to-I Human chr3 - 57573746 57573746 57573746 AAAACTCTGTCTCTACTAAAATTACAAAAATTAGCTGGTCGTGGTGGTGCATGTGTGTAACCCCA AAAACTCTGTCTCTACTAAAATTACAAAAATTGGCTGGTCGTGGTGGTGCATGTGTGTAACCCCA T C ARF4 Ensembl:ENSG00000168374 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs773434564 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123839,RMVar_hsa_circ_127739,RMVar_hsa_circ_219100,RMVar_hsa_circ_219102,RMVar_hsa_circ_92045,RMVar_hsa_circ_219101 29864 RMVar_ID_29864 Human_SNP_ID_134576399 A-to-I Human chr3 - 57577888 57577888 57577888 ACCACACCTGGCTAATTTTTGTATTTTTTTGTAGAGATGACCTTTCGCCATGTTGCCCAGGCTGG ACCACACCTGGCTAATTTTTGTATTTTTTTGTGGAGATGACCTTTCGCCATGTTGCCCAGGCTGG T C ARF4 Ensembl:ENSG00000168374 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1232104568 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14908850 RMVar_hsa_circ_123839,RMVar_hsa_circ_219102,RMVar_hsa_circ_361131,RMVar_hsa_circ_341967,RMVar_hsa_circ_274668,RMVar_hsa_circ_219105,RMVar_hsa_circ_219103,RMVar_hsa_circ_348493 29865 RMVar_ID_29865 Human_SNP_ID_134576549 A-to-I Human chr3 - 57578526 57578526 57578526 GCAGTGAGCCAAGATTGTGCTACTGTGCTCCTAGGCAACAGAGTTGAGACCCTGTCTGAGAAAAG GCAGTGAGCCAAGATTGTGCTACTGTGCTCCTGGGCAACAGAGTTGAGACCCTGTCTGAGAAAAG T C ARF4 Ensembl:ENSG00000168374 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559862406 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14908870,Human_RBP_ID_25748547 RMVar_hsa_circ_123839,RMVar_hsa_circ_219102,RMVar_hsa_circ_361131,RMVar_hsa_circ_341967,RMVar_hsa_circ_274668,RMVar_hsa_circ_219105,RMVar_hsa_circ_219103,RMVar_hsa_circ_348493 29866 RMVar_ID_29866 Human_SNP_ID_134576686 A-to-I Human chr3 - 57579080 57579080 57579080 TTTCACCAGGCTGATCTCGAACTCCTGATCTCAGGTGATCCACCTGCCTCGGCCTCCCAGAATGC TTTCACCAGGCTGATCTCGAACTCCTGATCTCGGGTGATCCACCTGCCTCGGCCTCCCAGAATGC T C ARF4 Ensembl:ENSG00000168374 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968703578 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14908881 RMVar_hsa_circ_123839,RMVar_hsa_circ_219102,RMVar_hsa_circ_361131,RMVar_hsa_circ_341967,RMVar_hsa_circ_274668,RMVar_hsa_circ_219105,RMVar_hsa_circ_219103,RMVar_hsa_circ_348493 29867 RMVar_ID_29867 Human_SNP_ID_134576699 A-to-I Human chr3 - 57579140 57579140 57579140 CTGGGATTACAGGTGTGCCACCATGCCCGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCA CTGGGATTACAGGTGTGCCACCATGCCCGGCTGATTTTTGTATTTTTAGTAGAGATGGGGTTTCA T C ARF4 Ensembl:ENSG00000168374 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs868768469 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123839,RMVar_hsa_circ_219102,RMVar_hsa_circ_361131,RMVar_hsa_circ_341967,RMVar_hsa_circ_274668,RMVar_hsa_circ_219105,RMVar_hsa_circ_219103,RMVar_hsa_circ_348493 29868 RMVar_ID_29868 Human_SNP_ID_134576719 A-to-I Human chr3 - 57579215 57579215 57579215 TAGTTTGCTCTTGTCGCCCAGGCTGGAGTGCAATGGCGCCATCTCGGCTCACTGCAGCCTCCGCC TAGTTTGCTCTTGTCGCCCAGGCTGGAGTGCAGTGGCGCCATCTCGGCTCACTGCAGCCTCCGCC T C ARF4 Ensembl:ENSG00000168374 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559901608 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123839,RMVar_hsa_circ_219102,RMVar_hsa_circ_361131,RMVar_hsa_circ_341967,RMVar_hsa_circ_274668,RMVar_hsa_circ_219105,RMVar_hsa_circ_219103,RMVar_hsa_circ_348493 29869 RMVar_ID_29869 Human_SNP_ID_134576797 A-to-I Human chr3 - 57579425 57579425 57579425 AAATTAGCCAGGTGTAATGGTGGGCGCCTGTAATCTCAGCTACTCAGGAGGCTGAGGCAGGAGAA AAATTAGCCAGGTGTAATGGTGGGCGCCTGTAGTCTCAGCTACTCAGGAGGCTGAGGCAGGAGAA T C ARF4 Ensembl:ENSG00000168374 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1284677503 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123839,RMVar_hsa_circ_219102,RMVar_hsa_circ_361131,RMVar_hsa_circ_341967,RMVar_hsa_circ_274668,RMVar_hsa_circ_219105,RMVar_hsa_circ_219103,RMVar_hsa_circ_348493 29870 RMVar_ID_29870 Human_SNP_ID_134576804 A-to-I Human chr3 - 57579448 57579445 57579448 TCTCATCTCTACTAAAAATACAAAAATTAGCCAGGTGTAATGGTGGGCGCCTGTAATCTCAGCTA TCTCATCTCTACTAAAAATACAAAAATTAGCC___TGTAATGGTGGGCGCCTGTAATCTCAGCTA ACCT A ARF4 Ensembl:ENSG00000168374 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1020526760 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_123839,RMVar_hsa_circ_219102,RMVar_hsa_circ_361131,RMVar_hsa_circ_341967,RMVar_hsa_circ_274668,RMVar_hsa_circ_219105,RMVar_hsa_circ_219103,RMVar_hsa_circ_348493 29871 RMVar_ID_29871 Human_SNP_ID_134576915 A-to-I Human chr3 - 57579927 57579927 57579927 CCTACTAAAATTTTAATTTTTTTCGTAGAGACAGGGTCTTACTCTGCCCAGGGTGATCTTGAACT CCTACTAAAATTTTAATTTTTTTCGTAGAGACGGGGTCTTACTCTGCCCAGGGTGATCTTGAACT T C ARF4 Ensembl:ENSG00000168374 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1238828450 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123839,RMVar_hsa_circ_219102,RMVar_hsa_circ_361131,RMVar_hsa_circ_341967,RMVar_hsa_circ_274668,RMVar_hsa_circ_219105,RMVar_hsa_circ_219103,RMVar_hsa_circ_348493 29872 RMVar_ID_29872 Human_SNP_ID_134576928 A-to-I Human chr3 - 57579993 57579993 57579993 GGGCTCATGTGATCCTCCCTTCTCAGCTTCCTAAGTAGCTAGGACTATAGACATGTGCCACCATG GGGCTCATGTGATCCTCCCTTCTCAGCTTCCTGAGTAGCTAGGACTATAGACATGTGCCACCATG T C ARF4 Ensembl:ENSG00000168374 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335985538 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25748556 RMVar_hsa_circ_123839,RMVar_hsa_circ_219102,RMVar_hsa_circ_361131,RMVar_hsa_circ_341967,RMVar_hsa_circ_274668,RMVar_hsa_circ_219105,RMVar_hsa_circ_219103,RMVar_hsa_circ_348493 29873 RMVar_ID_29873 Human_SNP_ID_134576943 A-to-I Human chr3 - 57580074 57580074 57580074 TTGAGATGGGGTCTCACTCTGTTACCCAGGCTAGAGTGCAGTGGCATGATCATGGCTCACTGTAG TTGAGATGGGGTCTCACTCTGTTACCCAGGCTGGAGTGCAGTGGCATGATCATGGCTCACTGTAG T C ARF4 Ensembl:ENSG00000168374 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1284429299 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123839,RMVar_hsa_circ_219102,RMVar_hsa_circ_361131,RMVar_hsa_circ_341967,RMVar_hsa_circ_274668,RMVar_hsa_circ_219105,RMVar_hsa_circ_219103,RMVar_hsa_circ_348493 29874 RMVar_ID_29874 Human_SNP_ID_134576948 A-to-I Human chr3 - 57580091 57580091 57580091 AACATTATTTTTTGTTTTTGAGATGGGGTCTCACTCTGTTACCCAGGCTAGAGTGCAGTGGCATG AACATTATTTTTTGTTTTTGAGATGGGGTCTCGCTCTGTTACCCAGGCTAGAGTGCAGTGGCATG T C ARF4 Ensembl:ENSG00000168374 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1056058109 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123839,RMVar_hsa_circ_219102,RMVar_hsa_circ_361131,RMVar_hsa_circ_341967,RMVar_hsa_circ_274668,RMVar_hsa_circ_219105,RMVar_hsa_circ_219103,RMVar_hsa_circ_348493 29875 RMVar_ID_29875 Human_SNP_ID_134577043 A-to-I Human chr3 - 57580534 57580534 57580534 ACCTGGGCATGGTGGCATACTCCTGTAGTCCCAGCTACTTGAGAGGCTGAGGTGGGAGGATCACC ACCTGGGCATGGTGGCATACTCCTGTAGTCCCGGCTACTTGAGAGGCTGAGGTGGGAGGATCACC T C ARF4 Ensembl:ENSG00000168374 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs936148974 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123839,RMVar_hsa_circ_219102,RMVar_hsa_circ_361131,RMVar_hsa_circ_341967,RMVar_hsa_circ_274668,RMVar_hsa_circ_219105,RMVar_hsa_circ_219103,RMVar_hsa_circ_348493 29876 RMVar_ID_29876 Human_SNP_ID_134577295 A-to-I Human chr3 - 57581644 57581644 57581644 AGGCATGCGCCACCACACCTGGCTAATTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTAG AGGCATGCGCCACCACACCTGGCTAATTTTGTTTTTTTAGTAGAGACGGGGTTTCACCATGTTAG T A ARF4 Ensembl:ENSG00000168374 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs920218918 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123839,RMVar_hsa_circ_219102,RMVar_hsa_circ_361131,RMVar_hsa_circ_341967,RMVar_hsa_circ_274668,RMVar_hsa_circ_219105,RMVar_hsa_circ_219103,RMVar_hsa_circ_348493 29877 RMVar_ID_29877 Human_SNP_ID_134577308 A-to-I Human chr3 - 57581691 57581691 57581691 GGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTTCAGGCATGCGCCACCACAC GGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAGGTAGCTGGGACTTCAGGCATGCGCCACCACAC T C ARF4 Ensembl:ENSG00000168374 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs944104724 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123839,RMVar_hsa_circ_219102,RMVar_hsa_circ_361131,RMVar_hsa_circ_341967,RMVar_hsa_circ_274668,RMVar_hsa_circ_219105,RMVar_hsa_circ_219103,RMVar_hsa_circ_348493 29878 RMVar_ID_29878 Human_SNP_ID_134579995 A-to-I Human chr3 - 57592304 57592304 57592304 TTTCATATTTGTAGTAGAGAGGGTTTCACCATATTGGTCAAGCTGGTCTCAAACTCCTGACCTCA TTTCATATTTGTAGTAGAGAGGGTTTCACCATGTTGGTCAAGCTGGTCTCAAACTCCTGACCTCA T C ARF4 Ensembl:ENSG00000168374 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1218141433 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76920,RMVar_hsa_circ_219107 29879 RMVar_ID_29879 Human_SNP_ID_134579996 A-to-I Human chr3 - 57592306 57592306 57592306 ATTTTCATATTTGTAGTAGAGAGGGTTTCACCATATTGGTCAAGCTGGTCTCAAACTCCTGACCT ATTTTCATATTTGTAGTAGAGAGGGTTTCACCGTATTGGTCAAGCTGGTCTCAAACTCCTGACCT T C ARF4 Ensembl:ENSG00000168374 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1447942499 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76920,RMVar_hsa_circ_219107 29880 RMVar_ID_29880 Human_SNP_ID_134589169 A-to-I Human chr3 - 57626547 57626547 57626547 GTGCCACCACGCCTGGCTAATTTTGTATTTTTAGTAGAGATGGGGTTTCTCCATGTTGGTCAGGC GTGCCACCACGCCTGGCTAATTTTGTATTTTTGGTAGAGATGGGGTTTCTCCATGTTGGTCAGGC T C DENND6A Ensembl:ENSG00000174839 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1269358904 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_156060 RMVar_hsa_circ_112781,RMVar_hsa_circ_219109 29881 RMVar_ID_29881 Human_SNP_ID_134589190 A-to-I Human chr3 - 57626646 57626646 57626646 GGAGTGCAATGGCGCAATCTCGGCTGACTGCAACCTCCACCTCCCGGGTGCAAGTGATTGTCCTG GGAGTGCAATGGCGCAATCTCGGCTGACTGCAGCCTCCACCTCCCGGGTGCAAGTGATTGTCCTG T C DENND6A Ensembl:ENSG00000174839 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560833732 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247852,Human_RBP_ID_606786,Human_RBP_ID_14909604 RMVar_hsa_circ_112781,RMVar_hsa_circ_219109 29882 RMVar_ID_29882 Human_SNP_ID_134589191 A-to-I Human chr3 - 57626647 57626647 57626647 TGGAGTGCAATGGCGCAATCTCGGCTGACTGCAACCTCCACCTCCCGGGTGCAAGTGATTGTCCT TGGAGTGCAATGGCGCAATCTCGGCTGACTGCGACCTCCACCTCCCGGGTGCAAGTGATTGTCCT T C DENND6A Ensembl:ENSG00000174839 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1471526011 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247852,Human_RBP_ID_606786,Human_RBP_ID_14909604 RMVar_hsa_circ_112781,RMVar_hsa_circ_219109 29883 RMVar_ID_29883 Human_SNP_ID_134589195 A-to-I Human chr3 - 57626662 57626662 57626662 TCTTGTTGCCCAGGCTGGAGTGCAATGGCGCAATCTCGGCTGACTGCAACCTCCACCTCCCGGGT TCTTGTTGCCCAGGCTGGAGTGCAATGGCGCAGTCTCGGCTGACTGCAACCTCCACCTCCCGGGT T C DENND6A Ensembl:ENSG00000174839 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1235838884 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_606786 RMVar_hsa_circ_112781,RMVar_hsa_circ_219109 29884 RMVar_ID_29884 Human_SNP_ID_134589353 A-to-I Human chr3 - 57627425 57627425 57627425 TAATTTAAACATTAGGCTGGGTGTGGTGGCTCACGCCTGTAATCCTAGCACTTTGGGAGGCCAAG TAATTTAAACATTAGGCTGGGTGTGGTGGCTCGCGCCTGTAATCCTAGCACTTTGGGAGGCCAAG T C DENND6A Ensembl:ENSG00000174839 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs150379083 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112781,RMVar_hsa_circ_219109 29885 RMVar_ID_29885 Human_SNP_ID_134597296 A-to-I Human chr3 - 57660313 57660313 57660313 AACGGGGCATGGTGGTGCACACCTGTAGTCCTAGGTACTTGGGATATTGCTTGAGCCTGGGAAGT AACGGGGCATGGTGGTGCACACCTGTAGTCCTGGGTACTTGGGATATTGCTTGAGCCTGGGAAGT T C DENND6A Ensembl:ENSG00000174839 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs955388432 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112781,RMVar_hsa_circ_219109,RMVar_hsa_circ_92125,RMVar_hsa_circ_219113,RMVar_hsa_circ_363853,RMVar_hsa_circ_29344,RMVar_hsa_circ_102377,RMVar_hsa_circ_219116,RMVar_hsa_circ_16778,RMVar_hsa_circ_219118,RMVar_hsa_circ_316854,RMVar_hsa_circ_344508,RMVar_hsa_circ_353267,RMVar_hsa_circ_335710,RMVar_hsa_circ_219119,RMVar_hsa_circ_219122,RMVar_hsa_circ_295990,RMVar_hsa_circ_324821,RMVar_hsa_circ_339339,RMVar_hsa_circ_310102,RMVar_hsa_circ_116821,RMVar_hsa_circ_271223,RMVar_hsa_circ_219124,RMVar_hsa_circ_219125,RMVar_hsa_circ_285398,RMVar_hsa_circ_334640,RMVar_hsa_circ_282231,RMVar_hsa_circ_219126,RMVar_hsa_circ_219127,RMVar_hsa_circ_40272 29886 RMVar_ID_29886 Human_SNP_ID_134597303 A-to-I Human chr3 - 57660344 57660344 57660344 AAACCTTGTCTCTACAAAAAATAAAAAAATTAACGGGGCATGGTGGTGCACACCTGTAGTCCTAG AAACCTTGTCTCTACAAAAAATAAAAAAATTATCGGGGCATGGTGGTGCACACCTGTAGTCCTAG T A DENND6A Ensembl:ENSG00000174839 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs143853226 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112781,RMVar_hsa_circ_219109,RMVar_hsa_circ_92125,RMVar_hsa_circ_219113,RMVar_hsa_circ_363853,RMVar_hsa_circ_29344,RMVar_hsa_circ_102377,RMVar_hsa_circ_219116,RMVar_hsa_circ_16778,RMVar_hsa_circ_219118,RMVar_hsa_circ_316854,RMVar_hsa_circ_344508,RMVar_hsa_circ_353267,RMVar_hsa_circ_335710,RMVar_hsa_circ_219119,RMVar_hsa_circ_219122,RMVar_hsa_circ_295990,RMVar_hsa_circ_324821,RMVar_hsa_circ_339339,RMVar_hsa_circ_310102,RMVar_hsa_circ_116821,RMVar_hsa_circ_271223,RMVar_hsa_circ_219124,RMVar_hsa_circ_219125,RMVar_hsa_circ_285398,RMVar_hsa_circ_334640,RMVar_hsa_circ_282231,RMVar_hsa_circ_219126,RMVar_hsa_circ_219127,RMVar_hsa_circ_40272 29887 RMVar_ID_29887 Human_SNP_ID_134599482 A-to-I Human chr3 - 57669099 57669099 57669099 GGGAGGCTGAGGCGGACAGATAACTTGAGATCAGGAATTCGAGACCAGCCTGGCCAACATGGTGA GGGAGGCTGAGGCGGACAGATAACTTGAGATCGGGAATTCGAGACCAGCCTGGCCAACATGGTGA T C DENND6A Ensembl:ENSG00000174839 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs926675497 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112781,RMVar_hsa_circ_219109,RMVar_hsa_circ_92125,RMVar_hsa_circ_83519,RMVar_hsa_circ_219113,RMVar_hsa_circ_16778,RMVar_hsa_circ_219118,RMVar_hsa_circ_335710,RMVar_hsa_circ_339339,RMVar_hsa_circ_219125,RMVar_hsa_circ_282231,RMVar_hsa_circ_312277,RMVar_hsa_circ_219129,RMVar_hsa_circ_219128,RMVar_hsa_circ_282200 29888 RMVar_ID_29888 Human_SNP_ID_134601296 A-to-I Human chr3 - 57676317 57676317 57676317 GAAGGGCAGTGGTGTGATTTCAGCTCACTGCAACCTCTGCCTCCCAGGTTCAAGCCATTCTTGTG GAAGGGCAGTGGTGTGATTTCAGCTCACTGCAGCCTCTGCCTCCCAGGTTCAAGCCATTCTTGTG T C DENND6A Ensembl:ENSG00000174839 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1559828907 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112781,RMVar_hsa_circ_219109,RMVar_hsa_circ_83519,RMVar_hsa_circ_219118,RMVar_hsa_circ_219125,RMVar_hsa_circ_219128 29889 RMVar_ID_29889 Human_SNP_ID_134604181 A-to-I Human chr3 - 57688184 57688184 57688184 CGAGACCGCCGTAGCCAACATGGTAAAACCCCATCTCTAATAAAAAAATACAAAAATAGGCAGCT CGAGACCGCCGTAGCCAACATGGTAAAACCCCTTCTCTAATAAAAAAATACAAAAATAGGCAGCT T A DENND6A Ensembl:ENSG00000174839 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7432266 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112781,RMVar_hsa_circ_219109,RMVar_hsa_circ_83519,RMVar_hsa_circ_219128 29890 RMVar_ID_29890 Human_SNP_ID_134604182 A-to-I Human chr3 - 57688184 57688184 57688184 CGAGACCGCCGTAGCCAACATGGTAAAACCCCATCTCTAATAAAAAAATACAAAAATAGGCAGCT CGAGACCGCCGTAGCCAACATGGTAAAACCCCGTCTCTAATAAAAAAATACAAAAATAGGCAGCT T C DENND6A Ensembl:ENSG00000174839 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7432266 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112781,RMVar_hsa_circ_219109,RMVar_hsa_circ_83519,RMVar_hsa_circ_219128 29891 RMVar_ID_29891 Human_SNP_ID_134622792 A-to-I Human chr3 + 57760867 57760867 57760867 CTCCTGCCTCAGCTTCCCGAGTAGCTGGGACTACAGGCATGCGCCACCACGCGTGGCTAATTTTG CTCCTGCCTCAGCTTCCCGAGTAGCTGGGACTGCAGGCATGCGCCACCACGCGTGGCTAATTTTG A G SLMAP Ensembl:ENSG00000163681 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1487617266 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75685,RMVar_hsa_circ_219132 29892 RMVar_ID_29892 Human_SNP_ID_134623509 A-to-I Human chr3 + 57763543 57763542 57763543 GCAATCCACCCGCCCCGGCCTCCTAAAGAGTTAGGATTACAGGTGTGAGCCACCGCGCCCGGCCT GCAATCCACCCGCCCCGGCCTCCTAAAGAGTT_GGATTACAGGTGTGAGCCACCGCGCCCGGCCT TA T SLMAP Ensembl:ENSG00000163681 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1383451025 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_14910766,Human_RBP_ID_18812809 RMVar_hsa_circ_75685,RMVar_hsa_circ_219132 29893 RMVar_ID_29893 Human_SNP_ID_134627130 A-to-I Human chr3 + 57778652 57778652 57778652 GCTGGAGTGTGGTGGTGCAATCATAGCTCACCACAGCCTCAAACTCTTGGGCTCAAGCAATCTTC GCTGGAGTGTGGTGGTGCAATCATAGCTCACCGCAGCCTCAAACTCTTGGGCTCAAGCAATCTTC A G SLMAP Ensembl:ENSG00000163681 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs549872014 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75685,RMVar_hsa_circ_219132 29894 RMVar_ID_29894 Human_SNP_ID_134627499 A-to-I Human chr3 + 57780221 57780221 57780221 CATGCTGGAGTGCAGTGGCATGATCACTGCTCACTGCAGCCTTGACCTCCTGGGCTCAAGCCATC CATGCTGGAGTGCAGTGGCATGATCACTGCTCGCTGCAGCCTTGACCTCCTGGGCTCAAGCCATC A G SLMAP Ensembl:ENSG00000163681 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs955876525 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75685,RMVar_hsa_circ_219132 29895 RMVar_ID_29895 Human_SNP_ID_134641957 A-to-I Human chr3 + 57843946 57843946 57843946 GGGATTACAGGTGCATACCACCATGCCCAGCTAATTTTTGTGTTTTCAGTAGAGATGGGGTTTCA GGGATTACAGGTGCATACCACCATGCCCAGCTGATTTTTGTGTTTTCAGTAGAGATGGGGTTTCA A G SLMAP Ensembl:ENSG00000163681 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs757168043 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4859,RMVar_hsa_circ_71875,RMVar_hsa_circ_219133,RMVar_hsa_circ_75685,RMVar_hsa_circ_219132,RMVar_hsa_circ_293059,RMVar_hsa_circ_320322,RMVar_hsa_circ_351929,RMVar_hsa_circ_267951,RMVar_hsa_circ_219134,RMVar_hsa_circ_12507,RMVar_hsa_circ_55640,RMVar_hsa_circ_219136,RMVar_hsa_circ_219137,RMVar_hsa_circ_219135,RMVar_hsa_circ_292939,RMVar_hsa_circ_311624,RMVar_hsa_circ_343212,RMVar_hsa_circ_369131,RMVar_hsa_circ_329367,RMVar_hsa_circ_297534,RMVar_hsa_circ_282503,RMVar_hsa_circ_282637,RMVar_hsa_circ_122911,RMVar_hsa_circ_219138,RMVar_hsa_circ_219140,RMVar_hsa_circ_219142,RMVar_hsa_circ_219144,RMVar_hsa_circ_219145,RMVar_hsa_circ_219143,RMVar_hsa_circ_219141,RMVar_hsa_circ_219139 29896 RMVar_ID_29896 Human_SNP_ID_134643737 A-to-I Human chr3 + 57850896 57850896 57850896 AGCTCAGGCAATACACCCACTTCAGCCTCCCAAAGTGTTGGGATTACAGGCATGAGCCATGGCGC AGCTCAGGCAATACACCCACTTCAGCCTCCCAGAGTGTTGGGATTACAGGCATGAGCCATGGCGC A G SLMAP Ensembl:ENSG00000163681 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956653369 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4572,RMVar_hsa_circ_4859,RMVar_hsa_circ_71875,RMVar_hsa_circ_219133,RMVar_hsa_circ_320322,RMVar_hsa_circ_351929,RMVar_hsa_circ_267951,RMVar_hsa_circ_219134,RMVar_hsa_circ_12507,RMVar_hsa_circ_55640,RMVar_hsa_circ_219136,RMVar_hsa_circ_219135,RMVar_hsa_circ_292939,RMVar_hsa_circ_311624,RMVar_hsa_circ_343212,RMVar_hsa_circ_369131,RMVar_hsa_circ_329367,RMVar_hsa_circ_282503,RMVar_hsa_circ_282637,RMVar_hsa_circ_122911,RMVar_hsa_circ_105364,RMVar_hsa_circ_219138,RMVar_hsa_circ_219140,RMVar_hsa_circ_219142,RMVar_hsa_circ_219144,RMVar_hsa_circ_219143,RMVar_hsa_circ_219141,RMVar_hsa_circ_219139,RMVar_hsa_circ_318609,RMVar_hsa_circ_351121,RMVar_hsa_circ_378605,RMVar_hsa_circ_343202,RMVar_hsa_circ_317810,RMVar_hsa_circ_272231,RMVar_hsa_circ_287096,RMVar_hsa_circ_124438,RMVar_hsa_circ_219148,RMVar_hsa_circ_219150,RMVar_hsa_circ_219152,RMVar_hsa_circ_219153,RMVar_hsa_circ_219151,RMVar_hsa_circ_219149,RMVar_hsa_circ_219147,RMVar_hsa_circ_53344,RMVar_hsa_circ_329058 29897 RMVar_ID_29897 Human_SNP_ID_134643740 A-to-I Human chr3 + 57850909 57850909 57850909 CACCCACTTCAGCCTCCCAAAGTGTTGGGATTACAGGCATGAGCCATGGCGCCCGGCCCATAGAT CACCCACTTCAGCCTCCCAAAGTGTTGGGATTGCAGGCATGAGCCATGGCGCCCGGCCCATAGAT A G SLMAP Ensembl:ENSG00000163681 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1009480996 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4572,RMVar_hsa_circ_4859,RMVar_hsa_circ_71875,RMVar_hsa_circ_219133,RMVar_hsa_circ_320322,RMVar_hsa_circ_351929,RMVar_hsa_circ_267951,RMVar_hsa_circ_219134,RMVar_hsa_circ_12507,RMVar_hsa_circ_55640,RMVar_hsa_circ_219136,RMVar_hsa_circ_219135,RMVar_hsa_circ_292939,RMVar_hsa_circ_311624,RMVar_hsa_circ_343212,RMVar_hsa_circ_369131,RMVar_hsa_circ_329367,RMVar_hsa_circ_282503,RMVar_hsa_circ_282637,RMVar_hsa_circ_122911,RMVar_hsa_circ_105364,RMVar_hsa_circ_219138,RMVar_hsa_circ_219140,RMVar_hsa_circ_219142,RMVar_hsa_circ_219144,RMVar_hsa_circ_219143,RMVar_hsa_circ_219141,RMVar_hsa_circ_219139,RMVar_hsa_circ_318609,RMVar_hsa_circ_351121,RMVar_hsa_circ_378605,RMVar_hsa_circ_343202,RMVar_hsa_circ_317810,RMVar_hsa_circ_272231,RMVar_hsa_circ_287096,RMVar_hsa_circ_124438,RMVar_hsa_circ_219148,RMVar_hsa_circ_219150,RMVar_hsa_circ_219152,RMVar_hsa_circ_219153,RMVar_hsa_circ_219151,RMVar_hsa_circ_219149,RMVar_hsa_circ_219147,RMVar_hsa_circ_53344,RMVar_hsa_circ_329058 29898 RMVar_ID_29898 Human_SNP_ID_134644098 A-to-I Human chr3 + 57852158 57852158 57852158 GGTCTCCAATCTCCTGACCTCGTTATCTGCCCACCTTGGCCTCCCAAAGTGCTGGGATTACAGGC GGTCTCCAATCTCCTGACCTCGTTATCTGCCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGC A G SLMAP Ensembl:ENSG00000163681 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1220254502 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4572,RMVar_hsa_circ_4859,RMVar_hsa_circ_71875,RMVar_hsa_circ_219133,RMVar_hsa_circ_320322,RMVar_hsa_circ_351929,RMVar_hsa_circ_267951,RMVar_hsa_circ_219134,RMVar_hsa_circ_12507,RMVar_hsa_circ_55640,RMVar_hsa_circ_219136,RMVar_hsa_circ_219135,RMVar_hsa_circ_292939,RMVar_hsa_circ_311624,RMVar_hsa_circ_343212,RMVar_hsa_circ_369131,RMVar_hsa_circ_329367,RMVar_hsa_circ_282503,RMVar_hsa_circ_282637,RMVar_hsa_circ_122911,RMVar_hsa_circ_105364,RMVar_hsa_circ_219138,RMVar_hsa_circ_219140,RMVar_hsa_circ_219142,RMVar_hsa_circ_219144,RMVar_hsa_circ_219143,RMVar_hsa_circ_219141,RMVar_hsa_circ_219139,RMVar_hsa_circ_318609,RMVar_hsa_circ_351121,RMVar_hsa_circ_378605,RMVar_hsa_circ_343202,RMVar_hsa_circ_317810,RMVar_hsa_circ_272231,RMVar_hsa_circ_287096,RMVar_hsa_circ_124438,RMVar_hsa_circ_219148,RMVar_hsa_circ_219150,RMVar_hsa_circ_219152,RMVar_hsa_circ_219153,RMVar_hsa_circ_219151,RMVar_hsa_circ_219149,RMVar_hsa_circ_219147,RMVar_hsa_circ_53344,RMVar_hsa_circ_329058 29899 RMVar_ID_29899 Human_SNP_ID_134654587 A-to-I Human chr3 + 57892975 57892975 57892975 CCTGCCTTAGCCTCCCAAGTAGCTGGGAGTACAGGTACCCACTACCACGCCTGGCTAATTTTTTG CCTGCCTTAGCCTCCCAAGTAGCTGGGAGTACGGGTACCCACTACCACGCCTGGCTAATTTTTTG A G SLMAP Ensembl:ENSG00000163681 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1404030254 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_219133,RMVar_hsa_circ_12507,RMVar_hsa_circ_55640,RMVar_hsa_circ_329367,RMVar_hsa_circ_122911,RMVar_hsa_circ_105364,RMVar_hsa_circ_219138,RMVar_hsa_circ_219139,RMVar_hsa_circ_351121,RMVar_hsa_circ_124438,RMVar_hsa_circ_219152,RMVar_hsa_circ_219153,RMVar_hsa_circ_219151,RMVar_hsa_circ_2272,RMVar_hsa_circ_31793,RMVar_hsa_circ_63841,RMVar_hsa_circ_338063,RMVar_hsa_circ_72009,RMVar_hsa_circ_321975,RMVar_hsa_circ_65306,RMVar_hsa_circ_30554,RMVar_hsa_circ_53444,RMVar_hsa_circ_308080,RMVar_hsa_circ_99828,RMVar_hsa_circ_8865,RMVar_hsa_circ_270279,RMVar_hsa_circ_219160,RMVar_hsa_circ_219161,RMVar_hsa_circ_317547,RMVar_hsa_circ_345248,RMVar_hsa_circ_266248,RMVar_hsa_circ_267420,RMVar_hsa_circ_61387,RMVar_hsa_circ_219163,RMVar_hsa_circ_219164,RMVar_hsa_circ_219165,RMVar_hsa_circ_219162,RMVar_hsa_circ_378452 29900 RMVar_ID_29900 Human_SNP_ID_134654603 A-to-I Human chr3 + 57893040 57893040 57893040 TAGTTTTAGTAGAGATGGAGTTTCACTGTGTTACCCAGGATGGTCTCGATCTCCTGACCTCTTGA TAGTTTTAGTAGAGATGGAGTTTCACTGTGTTGCCCAGGATGGTCTCGATCTCCTGACCTCTTGA A G SLMAP Ensembl:ENSG00000163681 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1450206313 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_219133,RMVar_hsa_circ_12507,RMVar_hsa_circ_55640,RMVar_hsa_circ_329367,RMVar_hsa_circ_122911,RMVar_hsa_circ_105364,RMVar_hsa_circ_219138,RMVar_hsa_circ_219139,RMVar_hsa_circ_351121,RMVar_hsa_circ_124438,RMVar_hsa_circ_219152,RMVar_hsa_circ_219153,RMVar_hsa_circ_219151,RMVar_hsa_circ_2272,RMVar_hsa_circ_31793,RMVar_hsa_circ_63841,RMVar_hsa_circ_338063,RMVar_hsa_circ_72009,RMVar_hsa_circ_321975,RMVar_hsa_circ_65306,RMVar_hsa_circ_30554,RMVar_hsa_circ_53444,RMVar_hsa_circ_308080,RMVar_hsa_circ_99828,RMVar_hsa_circ_8865,RMVar_hsa_circ_270279,RMVar_hsa_circ_219160,RMVar_hsa_circ_219161,RMVar_hsa_circ_317547,RMVar_hsa_circ_345248,RMVar_hsa_circ_266248,RMVar_hsa_circ_267420,RMVar_hsa_circ_61387,RMVar_hsa_circ_219163,RMVar_hsa_circ_219164,RMVar_hsa_circ_219165,RMVar_hsa_circ_219162,RMVar_hsa_circ_378452 29901 RMVar_ID_29901 Human_SNP_ID_134655169 A-to-I Human chr3 + 57895536 57895536 57895536 TTTTGTATTTTTTGTAGAGATGGGGTTTCACCATCTTGGCCATGCTGGTCTTGAACTCCTGACCT TTTTGTATTTTTTGTAGAGATGGGGTTTCACCGTCTTGGCCATGCTGGTCTTGAACTCCTGACCT A G SLMAP Ensembl:ENSG00000163681 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs980400297 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_219133,RMVar_hsa_circ_12507,RMVar_hsa_circ_55640,RMVar_hsa_circ_329367,RMVar_hsa_circ_122911,RMVar_hsa_circ_105364,RMVar_hsa_circ_219138,RMVar_hsa_circ_219139,RMVar_hsa_circ_351121,RMVar_hsa_circ_124438,RMVar_hsa_circ_219152,RMVar_hsa_circ_219153,RMVar_hsa_circ_219151,RMVar_hsa_circ_2272,RMVar_hsa_circ_31793,RMVar_hsa_circ_63841,RMVar_hsa_circ_338063,RMVar_hsa_circ_72009,RMVar_hsa_circ_321975,RMVar_hsa_circ_65306,RMVar_hsa_circ_30554,RMVar_hsa_circ_53444,RMVar_hsa_circ_308080,RMVar_hsa_circ_99828,RMVar_hsa_circ_8865,RMVar_hsa_circ_270279,RMVar_hsa_circ_219160,RMVar_hsa_circ_219161,RMVar_hsa_circ_317547,RMVar_hsa_circ_345248,RMVar_hsa_circ_266248,RMVar_hsa_circ_267420,RMVar_hsa_circ_61387,RMVar_hsa_circ_219163,RMVar_hsa_circ_219164,RMVar_hsa_circ_219165,RMVar_hsa_circ_219162,RMVar_hsa_circ_378452 29902 RMVar_ID_29902 Human_SNP_ID_134656126 A-to-I Human chr3 + 57899629 57899629 57899629 GCTAAGTTGGTCAGGTTGGTCTTGAACTTCTGAGCTCAAGCGTTCCTCTCACCTCAGCCTCCCAC GCTAAGTTGGTCAGGTTGGTCTTGAACTTCTGGGCTCAAGCGTTCCTCTCACCTCAGCCTCCCAC A G SLMAP Ensembl:ENSG00000163681 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1386983070 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14913363 RMVar_hsa_circ_55640,RMVar_hsa_circ_122911,RMVar_hsa_circ_219138,RMVar_hsa_circ_124438,RMVar_hsa_circ_219153,RMVar_hsa_circ_2272,RMVar_hsa_circ_31793,RMVar_hsa_circ_63841,RMVar_hsa_circ_72009,RMVar_hsa_circ_65306,RMVar_hsa_circ_30554,RMVar_hsa_circ_99828,RMVar_hsa_circ_8865,RMVar_hsa_circ_219161,RMVar_hsa_circ_317547,RMVar_hsa_circ_345248,RMVar_hsa_circ_267420,RMVar_hsa_circ_61387,RMVar_hsa_circ_219163,RMVar_hsa_circ_219162,RMVar_hsa_circ_334466 29903 RMVar_ID_29903 Human_SNP_ID_134656128 A-to-I Human chr3 + 57899634 57899634 57899634 GTTGGTCAGGTTGGTCTTGAACTTCTGAGCTCAAGCGTTCCTCTCACCTCAGCCTCCCACCTCAG GTTGGTCAGGTTGGTCTTGAACTTCTGAGCTCGAGCGTTCCTCTCACCTCAGCCTCCCACCTCAG A G SLMAP Ensembl:ENSG00000163681 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs188281354 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55640,RMVar_hsa_circ_122911,RMVar_hsa_circ_219138,RMVar_hsa_circ_124438,RMVar_hsa_circ_219153,RMVar_hsa_circ_2272,RMVar_hsa_circ_31793,RMVar_hsa_circ_63841,RMVar_hsa_circ_72009,RMVar_hsa_circ_65306,RMVar_hsa_circ_30554,RMVar_hsa_circ_99828,RMVar_hsa_circ_8865,RMVar_hsa_circ_219161,RMVar_hsa_circ_317547,RMVar_hsa_circ_345248,RMVar_hsa_circ_267420,RMVar_hsa_circ_61387,RMVar_hsa_circ_219163,RMVar_hsa_circ_219162,RMVar_hsa_circ_334466 29904 RMVar_ID_29904 Human_SNP_ID_134656146 A-to-I Human chr3 + 57899687 57899687 57899687 CTCCCACCTCAGCTTCCCAAGTAGCTGGGACTACAGGCATGCACCACCCTACCCGACTTGTTTAC CTCCCACCTCAGCTTCCCAAGTAGCTGGGACTGCAGGCATGCACCACCCTACCCGACTTGTTTAC A G SLMAP Ensembl:ENSG00000163681 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs535206473 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55640,RMVar_hsa_circ_122911,RMVar_hsa_circ_219138,RMVar_hsa_circ_124438,RMVar_hsa_circ_219153,RMVar_hsa_circ_2272,RMVar_hsa_circ_31793,RMVar_hsa_circ_63841,RMVar_hsa_circ_72009,RMVar_hsa_circ_65306,RMVar_hsa_circ_30554,RMVar_hsa_circ_99828,RMVar_hsa_circ_8865,RMVar_hsa_circ_219161,RMVar_hsa_circ_317547,RMVar_hsa_circ_345248,RMVar_hsa_circ_267420,RMVar_hsa_circ_61387,RMVar_hsa_circ_219163,RMVar_hsa_circ_219162,RMVar_hsa_circ_334466 29905 RMVar_ID_29905 Human_SNP_ID_134658596 A-to-I Human chr3 + 57909315 57909315 57909315 CCTGAGGTCAGGAATTCGAGAGCAGTGTGGCCAACATGGTGAACCCCTGTCTCCACTAAAAATAC CCTGAGGTCAGGAATTCGAGAGCAGTGTGGCCGACATGGTGAACCCCTGTCTCCACTAAAAATAC A G SLMAP Ensembl:ENSG00000163681 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1313051444 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55640,RMVar_hsa_circ_122911,RMVar_hsa_circ_219138,RMVar_hsa_circ_124438,RMVar_hsa_circ_219153,RMVar_hsa_circ_36843,RMVar_hsa_circ_31793,RMVar_hsa_circ_63841,RMVar_hsa_circ_72009,RMVar_hsa_circ_30554,RMVar_hsa_circ_99828,RMVar_hsa_circ_8865,RMVar_hsa_circ_219161,RMVar_hsa_circ_345248,RMVar_hsa_circ_267420,RMVar_hsa_circ_61387,RMVar_hsa_circ_219162,RMVar_hsa_circ_34639,RMVar_hsa_circ_280574,RMVar_hsa_circ_302619,RMVar_hsa_circ_41247,RMVar_hsa_circ_350383,RMVar_hsa_circ_219166,RMVar_hsa_circ_55498 29906 RMVar_ID_29906 Human_SNP_ID_134659810 A-to-I Human chr3 + 57914273 57914273 57914273 TACAAAAAATACAACAAATTAGCCTGGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGTGAGAGG TACAAAAAATACAACAAATTAGCCTGGCCTGTGGTCCCAGCTACTCAGGAGGCTGAGGTGAGAGG A G SLMAP Ensembl:ENSG00000163681 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965913613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14913616 RMVar_hsa_circ_36843,RMVar_hsa_circ_31793,RMVar_hsa_circ_63841,RMVar_hsa_circ_99828,RMVar_hsa_circ_8865,RMVar_hsa_circ_219161,RMVar_hsa_circ_61387,RMVar_hsa_circ_34639,RMVar_hsa_circ_280574,RMVar_hsa_circ_41247,RMVar_hsa_circ_350383,RMVar_hsa_circ_219166 29907 RMVar_ID_29907 Human_SNP_ID_134683904 A-to-I Human chr3 + 58011115 58011115 58011115 TTTTGTATTCTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCTTGACCT TTTTGTATTCTTAGTAGAGATGGGGTTTCACCGTGTTGGCCAGGCTGGTCTCGAACTCTTGACCT A G FLNB Ensembl:ENSG00000136068 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1441034909 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92492,RMVar_hsa_circ_110075,RMVar_hsa_circ_219167,RMVar_hsa_circ_219168 29908 RMVar_ID_29908 Human_SNP_ID_134688060 A-to-I Human chr3 + 58028935 58028935 58028935 ACTGCACCTGGCCAAAAACATTTTAATAAATTAGCTGGGTATGGTGGTATGTGCCTGTAATCCTA ACTGCACCTGGCCAAAAACATTTTAATAAATTGGCTGGGTATGGTGGTATGTGCCTGTAATCCTA A G FLNB Ensembl:ENSG00000136068 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1039744422 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14914137 RMVar_hsa_circ_92492,RMVar_hsa_circ_110075,RMVar_hsa_circ_219167,RMVar_hsa_circ_219168 29909 RMVar_ID_29909 Human_SNP_ID_134689057 A-to-I Human chr3 + 58032936 58032936 58032936 ACTCCCTTCCCCGCCAAAAAAAAGCTAGGTGTAGTGACATGCACCTGTGGTCCCAGCTACTCAGG ACTCCCTTCCCCGCCAAAAAAAAGCTAGGTGTGGTGACATGCACCTGTGGTCCCAGCTACTCAGG A G FLNB Ensembl:ENSG00000136068 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs916619484 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92492,RMVar_hsa_circ_110075,RMVar_hsa_circ_219167,RMVar_hsa_circ_219168 29910 RMVar_ID_29910 Human_SNP_ID_134695499 A-to-I Human chr3 + 58060282 58060282 58060282 CTCATGCCTGTAATTCCAGCACTTTGGAAGGCAGAGGCGGGAGCATTGTTTGAGCCCGGGAGTTT CTCATGCCTGTAATTCCAGCACTTTGGAAGGCTGAGGCGGGAGCATTGTTTGAGCCCGGGAGTTT A T FLNB Ensembl:ENSG00000136068 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1161852765 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92492,RMVar_hsa_circ_110075,RMVar_hsa_circ_219167,RMVar_hsa_circ_219168 29911 RMVar_ID_29911 Human_SNP_ID_134709812 A-to-I Human chr3 + 58116719 58116719 58116719 CTCGGTTTTATAGAAGGGAAGTGATTTCCCTGAGGACTTTGGTCTTCTCTTCTCTTGGTTGTGGG CTCGGTTTTATAGAAGGGAAGTGATTTCCCTGGGGACTTTGGTCTTCTCTTCTCTTGGTTGTGGG A G FLNB Ensembl:ENSG00000136068 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879917495 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_359080,RMVar_hsa_circ_91076,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_17572,RMVar_hsa_circ_98479,RMVar_hsa_circ_219193,RMVar_hsa_circ_219195,RMVar_hsa_circ_219196,RMVar_hsa_circ_219194,RMVar_hsa_circ_269448,RMVar_hsa_circ_53706,RMVar_hsa_circ_98744,RMVar_hsa_circ_219197,RMVar_hsa_circ_219198,RMVar_hsa_circ_107205,RMVar_hsa_circ_115559,RMVar_hsa_circ_219200,RMVar_hsa_circ_291110,RMVar_hsa_circ_295896,RMVar_hsa_circ_105809,RMVar_hsa_circ_32016,RMVar_hsa_circ_95081,RMVar_hsa_circ_126525,RMVar_hsa_circ_219202,RMVar_hsa_circ_219204,RMVar_hsa_circ_219205,RMVar_hsa_circ_219203,RMVar_hsa_circ_355302,RMVar_hsa_circ_219206,RMVar_hsa_circ_115414,RMVar_hsa_circ_219207,RMVar_hsa_circ_219208,RMVar_hsa_circ_108627,RMVar_hsa_circ_83988,RMVar_hsa_circ_219212,RMVar_hsa_circ_78034,RMVar_hsa_circ_219213,RMVar_hsa_circ_219211,RMVar_hsa_circ_126764,RMVar_hsa_circ_20161,RMVar_hsa_circ_219214,RMVar_hsa_circ_219215 29912 RMVar_ID_29912 Human_SNP_ID_134716263 A-to-I Human chr3 + 58141197 58141197 58141197 ATCACCTGGGCCCAGAAGGTTGAGGCTGTAGTAAGCTGAGATTGCGCCACTGCACTCCAGCCTGG ATCACCTGGGCCCAGAAGGTTGAGGCTGTAGTGAGCTGAGATTGCGCCACTGCACTCCAGCCTGG A G FLNB Ensembl:ENSG00000136068 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1476237728 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25749737 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_77922,RMVar_hsa_circ_9008,RMVar_hsa_circ_219171,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_105809,RMVar_hsa_circ_32016,RMVar_hsa_circ_95081,RMVar_hsa_circ_219204,RMVar_hsa_circ_219205,RMVar_hsa_circ_219213,RMVar_hsa_circ_126764,RMVar_hsa_circ_20161,RMVar_hsa_circ_219215,RMVar_hsa_circ_123318,RMVar_hsa_circ_219235,RMVar_hsa_circ_128181,RMVar_hsa_circ_219216,RMVar_hsa_circ_369422,RMVar_hsa_circ_353500,RMVar_hsa_circ_76358,RMVar_hsa_circ_219220,RMVar_hsa_circ_219221,RMVar_hsa_circ_219222,RMVar_hsa_circ_112942,RMVar_hsa_circ_219223,RMVar_hsa_circ_76324,RMVar_hsa_circ_92411,RMVar_hsa_circ_219225,RMVar_hsa_circ_219224,RMVar_hsa_circ_85139,RMVar_hsa_circ_93933,RMVar_hsa_circ_219228,RMVar_hsa_circ_219229,RMVar_hsa_circ_104236,RMVar_hsa_circ_378145,RMVar_hsa_circ_81753,RMVar_hsa_circ_107111,RMVar_hsa_circ_285374,RMVar_hsa_circ_370864,RMVar_hsa_circ_219230,RMVar_hsa_circ_267721,RMVar_hsa_circ_374132,RMVar_hsa_circ_325376,RMVar_hsa_circ_370760,RMVar_hsa_circ_117593,RMVar_hsa_circ_108769,RMVar_hsa_circ_99458,RMVar_hsa_circ_91283,RMVar_hsa_circ_219239,RMVar_hsa_circ_78061,RMVar_hsa_circ_219241,RMVar_hsa_circ_219242,RMVar_hsa_circ_219240,RMVar_hsa_circ_219237,RMVar_hsa_circ_219238,RMVar_hsa_circ_219236,RMVar_hsa_circ_219231,RMVar_hsa_circ_219233,RMVar_hsa_circ_219234,RMVar_hsa_circ_219232,RMVar_hsa_circ_106405,RMVar_hsa_circ_360450,RMVar_hsa_circ_114259,RMVar_hsa_circ_219246,RMVar_hsa_circ_219247,RMVar_hsa_circ_62053 29913 RMVar_ID_29913 Human_SNP_ID_134720244 A-to-I Human chr3 + 58156064 58156064 58156064 CACCCTCCGACGACGCCCGCCGCCTCACTGTTATGAGCCTTCAGGTGAGATGCAAGGAAGCATCC CACCCTCCGACGACGCCCGCCGCCTCACTGTTCTGAGCCTTCAGGTGAGATGCAAGGAAGCATCC A C FLNB Ensembl:ENSG00000136068 Protein coding CDS GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs146509223 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_445895,Human_Splice_Rec_445983,Human_Splice_Rec_446073,Human_Splice_Rec_446163,Human_Splice_Rec_446249,Human_Splice_Rec_446287,Human_Splice_Rec_446309,Human_Splice_Rec_446311 Human_miRNA_ID_228477,Human_miRNA_ID_591321 RMVar_hsa_circ_92492,RMVar_hsa_circ_219168,RMVar_hsa_circ_119463,RMVar_hsa_circ_219196,RMVar_hsa_circ_32016,RMVar_hsa_circ_81753,RMVar_hsa_circ_267721,RMVar_hsa_circ_370760,RMVar_hsa_circ_108769,RMVar_hsa_circ_7589,RMVar_hsa_circ_219231,RMVar_hsa_circ_219233,RMVar_hsa_circ_219232,RMVar_hsa_circ_20324,RMVar_hsa_circ_219252,RMVar_hsa_circ_312754,RMVar_hsa_circ_59015,RMVar_hsa_circ_93955,RMVar_hsa_circ_219253,RMVar_hsa_circ_88289,RMVar_hsa_circ_126490,RMVar_hsa_circ_219255,RMVar_hsa_circ_219258,RMVar_hsa_circ_219257,RMVar_hsa_circ_373808 29914 RMVar_ID_29914 Human_SNP_ID_134752613 A-to-I Human chr3 + 58286394 58286394 58286394 GCCAGGCTGGTCTTGAGCTCCTGACTTCAAGCAGTCCACCTTCCTTAGCCTCCCAAAGTGCTGGG GCCAGGCTGGTCTTGAGCTCCTGACTTCAAGCCGTCCACCTTCCTTAGCCTCCCAAAGTGCTGGG A C ABHD6 Ensembl:ENSG00000163686 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223818751 Functional Loss SNV dbSNP153 33..33 33 - - - 29915 RMVar_ID_29915 Human_SNP_ID_134754704 A-to-I Human chr3 + 58292653 58292653 58292653 TCAAAGAGACCTCCAGCTGGGTGCGGTGGCTCAGGCCTGTAATCCTAGCACTTTGGGAGGCTGAG TCAAAGAGACCTCCAGCTGGGTGCGGTGGCTCGGGCCTGTAATCCTAGCACTTTGGGAGGCTGAG A G ABHD6 Ensembl:ENSG00000163686 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1376522383 Functional Loss SNV dbSNP153 33..33 33 - - - 29916 RMVar_ID_29916 Human_SNP_ID_134759135 A-to-I Human chr3 + 58310159 58310156 58310160 AGAGCCAGAGGTGGAGGCTGCAGTGAACTCTGATTGTACCACTGCACTTCAGCCTAGGTGACAGG AGAGCCAGAGGTGGAGGCTGCAGTGAACTC____TGTACCACTGCACTTCAGCCTAGGTGACAGG CTGAT C RPP14,HTD2 Ensembl:ENSG00000163684,Ensembl:ENSG00000255154 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1472726111 Functional Loss DEL dbSNP153 31..34 33 - - - 29917 RMVar_ID_29917 Human_SNP_ID_134760044 A-to-I Human chr3 + 58312796 58312796 58312796 TAGCCTGGCCAACGTGGTGAAACGCTTTCTCTACTGAAAATACAAAAATTAGCTGGGCATGGTGG TAGCCTGGCCAACGTGGTGAAACGCTTTCTCTGCTGAAAATACAAAAATTAGCTGGGCATGGTGG A G RPP14,HTD2 Ensembl:ENSG00000163684,Ensembl:ENSG00000255154 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1397965182 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_219276,RMVar_hsa_circ_96723 29918 RMVar_ID_29918 Human_SNP_ID_134760059 A-to-I Human chr3 + 58312850 58312850 58312850 GGGCATGGTGGCGCACGCTTGTAGTCCCAGCTACTTGGAAGACTGAGGCAGGAGAATTGCTTGAA GGGCATGGTGGCGCACGCTTGTAGTCCCAGCTGCTTGGAAGACTGAGGCAGGAGAATTGCTTGAA A G RPP14,HTD2 Ensembl:ENSG00000163684,Ensembl:ENSG00000255154 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1247152460 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_219276,RMVar_hsa_circ_96723 29919 RMVar_ID_29919 Human_SNP_ID_134760860 A-to-I Human chr3 + 58315676 58315672 58315676 AGTGCATGAACCTCCCTGTACATTTCTTTTTTATTTATTTATTTATTTTTGAAACAGAGTTTCGC AGTGCATGAACCTCCCTGTACATTTCTTT____TTTATTTATTTATTTTTGAAACAGAGTTTCGC TTTTA T RPP14,HTD2 Ensembl:ENSG00000163684,Ensembl:ENSG00000255154 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs553685266 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_7215702 RMVar_hsa_circ_219276,RMVar_hsa_circ_96723 29920 RMVar_ID_29920 Human_SNP_ID_134760862 A-to-I Human chr3 + 58315676 58315676 58315676 AGTGCATGAACCTCCCTGTACATTTCTTTTTTATTTATTTATTTATTTTTGAAACAGAGTTTCGC AGTGCATGAACCTCCCTGTACATTTCTTTTTTGTTTATTTATTTATTTTTGAAACAGAGTTTCGC A G RPP14,HTD2 Ensembl:ENSG00000163684,Ensembl:ENSG00000255154 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs997181434 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7215702 RMVar_hsa_circ_219276,RMVar_hsa_circ_96723 29921 RMVar_ID_29921 Human_SNP_ID_134760863 A-to-I Human chr3 + 58315676 58315676 58315676 AGTGCATGAACCTCCCTGTACATTTCTTTTTTATTTATTTATTTATTTTTGAAACAGAGTTTCGC AGTGCATGAACCTCCCTGTACATTTCTTTTTTTTTTATTTATTTATTTTTGAAACAGAGTTTCGC A T RPP14,HTD2 Ensembl:ENSG00000163684,Ensembl:ENSG00000255154 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs997181434 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7215702 RMVar_hsa_circ_219276,RMVar_hsa_circ_96723 29922 RMVar_ID_29922 Human_SNP_ID_134761636 A-to-I Human chr3 + 58318435 58318435 58318435 ATCCTGGCACTTTGGGAGGCTGCGGCAGGCGGATCACTTGAGGTCAGGAGTCCAAGACCAGCCTG ATCCTGGCACTTTGGGAGGCTGCGGCAGGCGGGTCACTTGAGGTCAGGAGTCCAAGACCAGCCTG A G RPP14,HTD2 Ensembl:ENSG00000163684,Ensembl:ENSG00000255154 Protein coding,Protein coding 3'UTR,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1199982804 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_606926 RMVar_hsa_circ_219276,RMVar_hsa_circ_96723 29923 RMVar_ID_29923 Human_SNP_ID_134761710 A-to-I Human chr3 + 58318657 58318656 58318658 AGATTGCACCACTGCACTGTAGCCTGAGTGACAGAGCGAGACCCTGTCTCAAGAAAGAAGTATTG AGATTGCACCACTGCACTGTAGCCTGAGTGAC__AGCGAGACCCTGTCTCAAGAAAGAAGTATTG CAG C RPP14 Ensembl:ENSG00000163684 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1236909983 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_14915109,Human_RBP_ID_18812922 RMVar_hsa_circ_219276,RMVar_hsa_circ_96723 29924 RMVar_ID_29924 Human_SNP_ID_134761750 A-to-I Human chr3 + 58318813 58318813 58318813 CTTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGTGAAACCCCATCTCTACTAAAAATACA CTTGAGGTCAGGAGTTCAAGACCAGCCTGGCCGACATGTGAAACCCCATCTCTACTAAAAATACA A G RPP14 Ensembl:ENSG00000163684 Protein coding 3'UTR GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1128246 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_446510 RMVar_hsa_circ_219276,RMVar_hsa_circ_96723 29925 RMVar_ID_29925 Human_SNP_ID_134761761 A-to-I Human chr3 + 58318860 58318860 58318860 ATCTCTACTAAAAATACAAAAACTAACCGGGCATGGTGGCGGGCACCTGTAATCCCAGCTACTTG ATCTCTACTAAAAATACAAAAACTAACCGGGCTTGGTGGCGGGCACCTGTAATCCCAGCTACTTG A T RPP14 Ensembl:ENSG00000163684 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1198756126 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_446510 RMVar_hsa_circ_219276,RMVar_hsa_circ_96723 29926 RMVar_ID_29926 Human_SNP_ID_134761780 A-to-I Human chr3 + 58318948 58318946 58318948 TTGAACCTGGGAGGTTGCAGTGAGCTGAAATCACACCACTGCACTTCAGCCTGGGTGACAGAGCA TTGAACCTGGGAGGTTGCAGTGAGCTGAAAT__CACCACTGCACTTCAGCCTGGGTGACAGAGCA TCA T RPP14 Ensembl:ENSG00000163684 Protein coding 3'UTR GSE100210;GSE107867 HepG2 cell line;ASD brains,temporal_cortex - 29129909,30559470 RNA-Seq:(High) rs201012230 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_25749862 RMVar_hsa_circ_219276,RMVar_hsa_circ_96723 29927 RMVar_ID_29927 Human_SNP_ID_134762395 A-to-I Human chr3 + 58321011 58321011 58321011 GGGTGTGGTGGTGCGTGCCTGTAATCCCAGCTACTCGGAGGCTGAGGCAGGAAGATTGCTTGAAC GGGTGTGGTGGTGCGTGCCTGTAATCCCAGCTGCTCGGAGGCTGAGGCAGGAAGATTGCTTGAAC A G RPP14 Ensembl:ENSG00000163684 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1253118737 Functional Loss SNV dbSNP153 33..33 33 - - - 29928 RMVar_ID_29928 Human_SNP_ID_134762722 A-to-I Human chr3 + 58322113 58322113 58322113 GAGTCTCGCTCTTATTGCCCAGGCTGGATTGCAATGGCACGATCTTGGTTCACTGTGGCCTCCGC GAGTCTCGCTCTTATTGCCCAGGCTGGATTGCCATGGCACGATCTTGGTTCACTGTGGCCTCCGC A C RPP14 Ensembl:ENSG00000163684 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs141480279 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14915247,Human_RBP_ID_27504329 29929 RMVar_ID_29929 Human_SNP_ID_134762764 A-to-I Human chr3 + 58322268 58322268 58322268 TTTAGTGGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTTTCGAACTCCTGACCTCAGGTGATC TTTAGTGGAGATGGGGTTTCACCATGTTGGCCGGGCTGGTTTCGAACTCCTGACCTCAGGTGATC A G RPP14 Ensembl:ENSG00000163684 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1220260375 Functional Loss SNV dbSNP153 33..33 33 - - - 29930 RMVar_ID_29930 Human_SNP_ID_134762922 A-to-I Human chr3 + 58322944 58322943 58322945 CACTGTTTTTTTTTTTGTTTGTTTTCTGAGACAGAGTCTCACTCTGTCTCCCAGGCTGGAGTTGC CACTGTTTTTTTTTTTGTTTGTTTTCTGAGAC__AGTCTCACTCTGTCTCCCAGGCTGGAGTTGC CAG C RPP14 Ensembl:ENSG00000163684 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1402064724 Functional Loss DEL dbSNP153 33..34 33 - - - 29931 RMVar_ID_29931 Human_SNP_ID_134762923 A-to-I Human chr3 + 58322944 58322944 58322944 CACTGTTTTTTTTTTTGTTTGTTTTCTGAGACAGAGTCTCACTCTGTCTCCCAGGCTGGAGTTGC CACTGTTTTTTTTTTTGTTTGTTTTCTGAGACGGAGTCTCACTCTGTCTCCCAGGCTGGAGTTGC A G RPP14 Ensembl:ENSG00000163684 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1455864067 Functional Loss SNV dbSNP153 33..33 33 - - - 29932 RMVar_ID_29932 Human_SNP_ID_134762924 A-to-I Human chr3 + 58322944 58322944 58322944 CACTGTTTTTTTTTTTGTTTGTTTTCTGAGACAGAGTCTCACTCTGTCTCCCAGGCTGGAGTTGC CACTGTTTTTTTTTTTGTTTGTTTTCTGAGACTGAGTCTCACTCTGTCTCCCAGGCTGGAGTTGC A T RPP14 Ensembl:ENSG00000163684 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1455864067 Functional Loss SNV dbSNP153 33..33 33 - - - 29933 RMVar_ID_29933 Human_SNP_ID_134764014 A-to-I Human chr3 + 58327451 58327451 58327451 TGCCTAGCTAATTGTGTAATTTTAGTAGAGACAGGGTTTTTGCATGTAGGTCAGGCTGGTCTCAA TGCCTAGCTAATTGTGTAATTTTAGTAGAGACCGGGTTTTTGCATGTAGGTCAGGCTGGTCTCAA A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947068469 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7215865,Human_RBP_ID_14915499 29934 RMVar_ID_29934 Human_SNP_ID_134764579 A-to-I Human chr3 + 58329907 58329907 58329907 CAGGTTTTCACCATGTTGTCCAGGCTGGTCTCAGACTTCTGACCTCAAGTGATGTGCCCGCCTCG CAGGTTTTCACCATGTTGTCCAGGCTGGTCTCCGACTTCTGACCTCAAGTGATGTGCCCGCCTCG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027220790 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14915570 29935 RMVar_ID_29935 Human_SNP_ID_134788761 A-to-I Human chr3 - 58427586 58427586 58427586 TTTTTTGAGACAATGTTTGGCTCTGTTCCCCAAGCTGGAGTGTGATGGCACAATCTTGGCTCACT TTTTTTGAGACAATGTTTGGCTCTGTTCCCCAGGCTGGAGTGTGATGGCACAATCTTGGCTCACT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1446350352 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2794624,Human_RBP_ID_7216126 29936 RMVar_ID_29936 Human_SNP_ID_135172302 A-to-I Human chr3 - 59909174 59909174 59909174 CAAAAAATTAGCTGGGTCGATGGTGCGTGCCTATAGTGCCAGCTACTCAGGAGGCTGAGGCAGGA CAAAAAATTAGCTGGGTCGATGGTGCGTGCCTGTAGTGCCAGCTACTCAGGAGGCTGAGGCAGGA T C FHIT Ensembl:ENSG00000189283 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1274430069 Functional Loss SNV dbSNP153 33..33 33 - - - 29937 RMVar_ID_29937 Human_SNP_ID_511208022 A-to-I Human chr12 - 92129467 92129467 92129467 GGATTTTTTTTTTTGAGACAGGGTCTCACTCTATCGCCAGGCTGGAGTGCAGTGGCGCGATCTCA GGATTTTTTTTTTTGAGACAGGGTCTCACTCTGTCGCCAGGCTGGAGTGCAGTGGCGCGATCTCA T C LINC01619 Ensembl:ENSG00000257242 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1429090798 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12053014 29938 RMVar_ID_29938 Human_SNP_ID_511208024 A-to-I Human chr12 - 92129472 92129468 92129472 TGTTAGGATTTTTTTTTTTGAGACAGGGTCTCACTCTATCGCCAGGCTGGAGTGCAGTGGCGCGA TGTTAGGATTTTTTTTTTTGAGACAGGGTCTC____TATCGCCAGGCTGGAGTGCAGTGGCGCGA AGAGT A LINC01619 Ensembl:ENSG00000257242 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1010284840 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_12053014 29939 RMVar_ID_29939 Human_SNP_ID_511304152 A-to-I Human chr12 - 92531139 92531139 92531139 GCAAAACCACAGTTGTTGACAGCCATAAGATTAGAGACAAGCACAAAGGGACAGGTCAACATGCC GCAAAACCACAGTTGTTGACAGCCATAAGATTGGAGACAAGCACAAAGGGACAGGTCAACATGCC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs925385135 Functional Loss SNV dbSNP153 33..33 33 - - - 29940 RMVar_ID_29940 Human_SNP_ID_511304163 A-to-I Human chr12 - 92531167 92531167 92531167 CATTGGGGAGTAAAGAGGGCATCCACCAGCAAAACCACAGTTGTTGACAGCCATAAGATTAGAGA CATTGGGGAGTAAAGAGGGCATCCACCAGCAAGACCACAGTTGTTGACAGCCATAAGATTAGAGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs943310682 Functional Loss SNV dbSNP153 33..33 33 - - - 29941 RMVar_ID_29941 Human_SNP_ID_511304171 A-to-I Human chr12 - 92531186 92531186 92531186 AATCTATCCATGCAGTATACATTGGGGAGTAAAGAGGGCATCCACCAGCAAAACCACAGTTGTTG AATCTATCCATGCAGTATACATTGGGGAGTAAGGAGGGCATCCACCAGCAAAACCACAGTTGTTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1040304737 Functional Loss SNV dbSNP153 33..33 33 - - - 29942 RMVar_ID_29942 Human_SNP_ID_511377167 A-to-I Human chr12 - 92835550 92835550 92835550 AAAATTAGCTGGGCATGGTGGCGGGCGCCTGTAGTCTTAGCTACTTGGGAGGCTGAGGCAAGAGA AAAATTAGCTGGGCATGGTGGCGGGCGCCTGTCGTCTTAGCTACTTGGGAGGCTGAGGCAAGAGA T G EEA1 Ensembl:ENSG00000102189 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1235282367 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_363815,RMVar_hsa_circ_54091,RMVar_hsa_circ_73433,RMVar_hsa_circ_45277,RMVar_hsa_circ_16484,RMVar_hsa_circ_26898,RMVar_hsa_circ_7116,RMVar_hsa_circ_63190,RMVar_hsa_circ_352858,RMVar_hsa_circ_269732,RMVar_hsa_circ_9581,RMVar_hsa_circ_58505,RMVar_hsa_circ_158749,RMVar_hsa_circ_287738,RMVar_hsa_circ_293224,RMVar_hsa_circ_158750,RMVar_hsa_circ_42353,RMVar_hsa_circ_63627,RMVar_hsa_circ_348148,RMVar_hsa_circ_308156,RMVar_hsa_circ_158752,RMVar_hsa_circ_158753,RMVar_hsa_circ_92908,RMVar_hsa_circ_275707,RMVar_hsa_circ_158754,RMVar_hsa_circ_158756,RMVar_hsa_circ_271037,RMVar_hsa_circ_367556,RMVar_hsa_circ_329609,RMVar_hsa_circ_19208,RMVar_hsa_circ_158755 29943 RMVar_ID_29943 Human_SNP_ID_511381465 A-to-I Human chr12 - 92855321 92855321 92855321 TGTTCACAGCATTCTCCTGCCTCAGCCTTCCTAGTAGCTGGGACTACAGGCACGTCCGCCATCAG TGTTCACAGCATTCTCCTGCCTCAGCCTTCCTGGTAGCTGGGACTACAGGCACGTCCGCCATCAG T C EEA1 Ensembl:ENSG00000102189 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs901982986 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54091,RMVar_hsa_circ_73433,RMVar_hsa_circ_45277,RMVar_hsa_circ_26898,RMVar_hsa_circ_58505,RMVar_hsa_circ_348148,RMVar_hsa_circ_60946,RMVar_hsa_circ_367556,RMVar_hsa_circ_19208,RMVar_hsa_circ_309256,RMVar_hsa_circ_338894,RMVar_hsa_circ_73196 29944 RMVar_ID_29944 Human_SNP_ID_511382220 A-to-I Human chr12 - 92858395 92858395 92858395 TCTGGTGACTGTTGCTCCAAGGCTACCAGCACATTACAAGTCTTGTAGTCAAACCCTTTGGAAGA TCTGGTGACTGTTGCTCCAAGGCTACCAGCACGTTACAAGTCTTGTAGTCAAACCCTTTGGAAGA T C EEA1 Ensembl:ENSG00000102189 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs879175631 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4291,RMVar_hsa_circ_54091,RMVar_hsa_circ_73433,RMVar_hsa_circ_26898,RMVar_hsa_circ_58505,RMVar_hsa_circ_348148,RMVar_hsa_circ_60946,RMVar_hsa_circ_367556,RMVar_hsa_circ_309256,RMVar_hsa_circ_73196 29945 RMVar_ID_29945 Human_SNP_ID_511385772 A-to-I Human chr12 - 92874199 92874199 92874199 CTCCCGCCTCAACCTCCTAAGTACCTGGGACTATAGGTGCATGCCACCATGCCTGGCTAAATTTT CTCCCGCCTCAACCTCCTAAGTACCTGGGACTGTAGGTGCATGCCACCATGCCTGGCTAAATTTT T C EEA1 Ensembl:ENSG00000102189 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1280597904 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54091,RMVar_hsa_circ_60946,RMVar_hsa_circ_73196 29946 RMVar_ID_29946 Human_SNP_ID_511386212 A-to-I Human chr12 - 92876189 92876189 92876189 ATGCACCTGTATTCTCAGCTACTCGGGAGGCTAAGGTGGGAGGATCGCTTGAGCCCAGCAGTTCG ATGCACCTGTATTCTCAGCTACTCGGGAGGCTCAGGTGGGAGGATCGCTTGAGCCCAGCAGTTCG T G EEA1 Ensembl:ENSG00000102189 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388282346 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54091,RMVar_hsa_circ_60946,RMVar_hsa_circ_73196 29947 RMVar_ID_29947 Human_SNP_ID_511414889 A-to-I Human chr12 + 92992652 92992652 92992652 TTTCACTCTTGTTGCCTAGGCTGGAGTGCAATAGCACAATCTCAGCTCACCGCAACCTCCACCCC TTTCACTCTTGTTGCCTAGGCTGGAGTGCAATCGCACAATCTCAGCTCACCGCAACCTCCACCCC A C LINC02413 RNACentral:URS00009C5281 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1402254693 Functional Loss SNV dbSNP153 33..33 33 - - - 29948 RMVar_ID_29948 Human_SNP_ID_511506801 A-to-I Human chr12 + 93382219 93382218 93382219 CTGGGAGGTGGAGGCTGCAGTGAGCCGAGATCATGCCATTGCACTCCAGCCTGGGCAACAGAGCA CTGGGAGGTGGAGGCTGCAGTGAGCCGAGATC_TGCCATTGCACTCCAGCCTGGGCAACAGAGCA CA C NUDT4 Ensembl:ENSG00000173598 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1334456323 Functional Loss DEL dbSNP153 33..33 33 - - - 29949 RMVar_ID_29949 Human_SNP_ID_511506998 A-to-I Human chr12 + 93382801 93382799 93382801 CAGGTTCACGCCATTCTCAAGTAGCTGGGACTACAGGCAGCCGCCACCATACCTGGCTAATTTTT CAGGTTCACGCCATTCTCAAGTAGCTGGGAC__CAGGCAGCCGCCACCATACCTGGCTAATTTTT CTA C NUDT4 Ensembl:ENSG00000173598 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1442183881 Functional Loss DEL dbSNP153 32..33 33 - - - 29950 RMVar_ID_29950 Human_SNP_ID_511506999 A-to-I Human chr12 + 93382801 93382801 93382801 CAGGTTCACGCCATTCTCAAGTAGCTGGGACTACAGGCAGCCGCCACCATACCTGGCTAATTTTT CAGGTTCACGCCATTCTCAAGTAGCTGGGACTGCAGGCAGCCGCCACCATACCTGGCTAATTTTT A G NUDT4 Ensembl:ENSG00000173598 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1279832747 Functional Loss SNV dbSNP153 33..33 33 - - - 29951 RMVar_ID_29951 Human_SNP_ID_511507016 A-to-I Human chr12 + 93382868 93382868 93382868 TATTTTTAGTAGAGAAGGGGTTTCACTGTGTTAGCCAGGATGGTCTTGATCTCCTGACCTTGTGA TATTTTTAGTAGAGAAGGGGTTTCACTGTGTTGGCCAGGATGGTCTTGATCTCCTGACCTTGTGA A G NUDT4 Ensembl:ENSG00000173598 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs923603873 Functional Loss SNV dbSNP153 33..33 33 - - - 29952 RMVar_ID_29952 Human_SNP_ID_511507395 A-to-I Human chr12 + 93384349 93384349 93384349 GCTACCACGCCCAGCTAATTTTTTGTATTTTTAGTAGAGACGGCGTTTCACTATGTTGGCCAGGA GCTACCACGCCCAGCTAATTTTTTGTATTTTTTGTAGAGACGGCGTTTCACTATGTTGGCCAGGA A T NUDT4 Ensembl:ENSG00000173598 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1436689357 Functional Loss SNV dbSNP153 33..33 33 - - - 29953 RMVar_ID_29953 Human_SNP_ID_511507400 A-to-I Human chr12 + 93384366 93384366 93384366 ATTTTTTGTATTTTTAGTAGAGACGGCGTTTCACTATGTTGGCCAGGATGGTCTTGATCTCCTGA ATTTTTTGTATTTTTAGTAGAGACGGCGTTTCCCTATGTTGGCCAGGATGGTCTTGATCTCCTGA A C NUDT4 Ensembl:ENSG00000173598 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1161236029 Functional Loss SNV dbSNP153 33..33 33 - - - 29954 RMVar_ID_29954 Human_SNP_ID_511507940 A-to-I Human chr12 + 93386160 93386160 93386160 ACCATGCCTGGCTAATTTATTGAGTTTTTTGTAGAGACAGGGTCTTCCTATGTTGCCTAGGCTGG ACCATGCCTGGCTAATTTATTGAGTTTTTTGTGGAGACAGGGTCTTCCTATGTTGCCTAGGCTGG A G NUDT4 Ensembl:ENSG00000173598 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1277368691 Functional Loss SNV dbSNP153 33..33 33 - - - 29955 RMVar_ID_29955 Human_SNP_ID_511508634 A-to-I Human chr12 + 93389325 93389325 93389325 AGAAACCCCGTCTCTACTAAAAATACAAAATTAGCTGGGCGTGGTGGCGCATGTCTGTAATCCCA AGAAACCCCGTCTCTACTAAAAATACAAAATTTGCTGGGCGTGGTGGCGCATGTCTGTAATCCCA A T NUDT4 Ensembl:ENSG00000173598 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1392955041 Functional Loss SNV dbSNP153 33..33 33 - - - 29956 RMVar_ID_29956 Human_SNP_ID_511508708 A-to-I Human chr12 + 93389641 93389641 93389641 ATCTGAAGCATAGACCGGGCGCGGTGGCTGACACCTGTAACCCCAGCACTTTGGGAGGCCGAGGC ATCTGAAGCATAGACCGGGCGCGGTGGCTGACGCCTGTAACCCCAGCACTTTGGGAGGCCGAGGC A G NUDT4 Ensembl:ENSG00000173598 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1412486451 Functional Loss SNV dbSNP153 33..33 33 - - - 29957 RMVar_ID_29957 Human_SNP_ID_511508949 A-to-I Human chr12 + 93390636 93390636 93390636 TAACCCCCCCTCCCTTTTTTTGAGACAGTCTCATTCTGTCGCCCAGGCTGGAGTGCAGTGGCATG TAACCCCCCCTCCCTTTTTTTGAGACAGTCTCTTTCTGTCGCCCAGGCTGGAGTGCAGTGGCATG A T NUDT4 Ensembl:ENSG00000173598 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs913752602 Functional Loss SNV dbSNP153 33..33 33 - - - 29958 RMVar_ID_29958 Human_SNP_ID_511509017 A-to-I Human chr12 + 93390933 93390933 93390933 TGCTTTTCTAAGAGGAGGTTCTATGCCTAAATAGATACTCTCTTTTAACTCAGCATTTTGGGGGC TGCTTTTCTAAGAGGAGGTTCTATGCCTAAATTGATACTCTCTTTTAACTCAGCATTTTGGGGGC A T NUDT4 Ensembl:ENSG00000173598 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs970566764 Functional Loss SNV dbSNP153 33..33 33 - - - 29959 RMVar_ID_29959 Human_SNP_ID_511509186 A-to-I Human chr12 + 93391633 93391633 93391633 GTGGTGGGTGCCTGTACTCCCAACTGCTCGGGAAGCTGGAGTGAGAGGATCACTTGAGCCCGGGA GTGGTGGGTGCCTGTACTCCCAACTGCTCGGGGAGCTGGAGTGAGAGGATCACTTGAGCCCGGGA A G NUDT4 Ensembl:ENSG00000173598 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs111602701 Functional Loss SNV dbSNP153 33..33 33 - - - 29960 RMVar_ID_29960 Human_SNP_ID_511509886 A-to-I Human chr12 + 93394072 93394072 93394072 TCACCCATGCTGGAGTATGGTGGCACGATCTCAGTTCATTGCAACCTCCACCTCCTGGGTTCAAG TCACCCATGCTGGAGTATGGTGGCACGATCTCGGTTCATTGCAACCTCCACCTCCTGGGTTCAAG A G NUDT4 Ensembl:ENSG00000173598 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2035052 Functional Loss SNV dbSNP153 33..33 33 - - - 29961 RMVar_ID_29961 Human_SNP_ID_511509887 A-to-I Human chr12 + 93394072 93394072 93394072 TCACCCATGCTGGAGTATGGTGGCACGATCTCAGTTCATTGCAACCTCCACCTCCTGGGTTCAAG TCACCCATGCTGGAGTATGGTGGCACGATCTCTGTTCATTGCAACCTCCACCTCCTGGGTTCAAG A T NUDT4 Ensembl:ENSG00000173598 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2035052 Functional Loss SNV dbSNP153 33..33 33 - - - 29962 RMVar_ID_29962 Human_SNP_ID_511510802 A-to-I Human chr12 + 93397705 93397705 93397705 CAACCACGCCCGGCTAATATTTTCGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGACAGGC CAACCACGCCCGGCTAATATTTTCGTATTTTTCGTAGAGACGGGGTTTCACCATGTTGGACAGGC A C NUDT4 Ensembl:ENSG00000173598 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs114047443 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_377729 29963 RMVar_ID_29963 Human_SNP_ID_511510803 A-to-I Human chr12 + 93397705 93397705 93397705 CAACCACGCCCGGCTAATATTTTCGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGACAGGC CAACCACGCCCGGCTAATATTTTCGTATTTTTGGTAGAGACGGGGTTTCACCATGTTGGACAGGC A G NUDT4 Ensembl:ENSG00000173598 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs114047443 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_377729 29964 RMVar_ID_29964 Human_SNP_ID_511510910 A-to-I Human chr12 + 93398184 93398184 93398184 CAACATGGTGAAACCCCGTCTGTACTAAAAATACAAAAATTAGCCAGGCGTGGTGGCGTGCACCT CAACATGGTGAAACCCCGTCTGTACTAAAAATGCAAAAATTAGCCAGGCGTGGTGGCGTGCACCT A G NUDT4 Ensembl:ENSG00000173598 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1033365905 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_377729 29965 RMVar_ID_29965 Human_SNP_ID_511511762 A-to-I Human chr12 + 93400837 93400837 93400837 CTTCATGTTGGTCAGGCTGGTCTCAAACTCCTAACCTCGTGATCCGCCTGCCTCGACCTCCCAAA CTTCATGTTGGTCAGGCTGGTCTCAAACTCCTGACCTCGTGATCCGCCTGCCTCGACCTCCCAAA A G NUDT4 Ensembl:ENSG00000173598 Protein coding 3'UTR GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1331060470 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26420511 29966 RMVar_ID_29966 Human_SNP_ID_511511779 A-to-I Human chr12 + 93400868 93400868 93400868 TAACCTCGTGATCCGCCTGCCTCGACCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCATGC TAACCTCGTGATCCGCCTGCCTCGACCTCCCAGAGTGCTGGGATTACAGGCATGAGCCACCATGC A G NUDT4 Ensembl:ENSG00000173598 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215970436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17243314 29967 RMVar_ID_29967 Human_SNP_ID_511513763 A-to-I Human chr12 - 93407137 93407137 93407137 CTTCCTGAAAATCGACTGCCCAGGCCGGGCACAGTGGCTCATGCCTGTAATCCCAGCACTTTAGG CTTCCTGAAAATCGACTGCCCAGGCCGGGCACCGTGGCTCATGCCTGTAATCCCAGCACTTTAGG T G UBE2N Ensembl:ENSG00000177889 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1263353179 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_429995 29968 RMVar_ID_29968 Human_SNP_ID_511521050 A-to-I Human chr12 - 93436772 93436772 93436772 TTATCTTCTGGACCAAAGCTCTTTTAGCCAATAAAAGTGACTGAAGCTGGGCATGGTGGTTCACA TTATCTTCTGGACCAAAGCTCTTTTAGCCAATGAAAGTGACTGAAGCTGGGCATGGTGGTTCACA T C UBE2N Ensembl:ENSG00000177889 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs763567680 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12056190,Human_RBP_ID_19817762 29969 RMVar_ID_29969 Human_SNP_ID_511521111 A-to-I Human chr12 - 93437045 93437045 93437045 TTGCCTAGGCTGTTCTCGAGCTCCTAGGCTCAAGTGATTCTTCCACCTCGGCCTCCCAAAGTGCT TTGCCTAGGCTGTTCTCGAGCTCCTAGGCTCACGTGATTCTTCCACCTCGGCCTCCCAAAGTGCT T G UBE2N Ensembl:ENSG00000177889 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs969623335 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12056208 29970 RMVar_ID_29970 Human_SNP_ID_511521685 A-to-I Human chr12 - 93439354 93439347 93439354 CCACTTAAGCCTCTTCAATAGCTGGGACTGCAAGGTGCATGCCACCACACCCAGCTAATTTTTGT CCACTTAAGCCTCTTCAATAGCTGGGACTGCA_______TGCCACCACACCCAGCTAATTTTTGT ATGCACCT A UBE2N Ensembl:ENSG00000177889 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1440970526 Functional Loss DEL dbSNP153 33..39 33 - - - 29971 RMVar_ID_29971 Human_SNP_ID_511530715 A-to-I Human chr12 + 93475396 93475396 93475396 CCCTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGCGCCTGGCGAATATTTGACTTT CCCTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCGCCTGGCGAATATTTGACTTT A G MRPL42 Ensembl:ENSG00000198015 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1021744356 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12097,RMVar_hsa_circ_26239,RMVar_hsa_circ_41575,RMVar_hsa_circ_316516,RMVar_hsa_circ_14974,RMVar_hsa_circ_332591,RMVar_hsa_circ_112019,RMVar_hsa_circ_158763,RMVar_hsa_circ_158764 29972 RMVar_ID_29972 Human_SNP_ID_511530881 A-to-I Human chr12 + 93475968 93475968 93475968 GCACCACTGCACTCCAGCCTGGGAGACAGAGCAAGACTCCGTCTCAAAAACAAAACAAAACAACA GCACCACTGCACTCCAGCCTGGGAGACAGAGCGAGACTCCGTCTCAAAAACAAAACAAAACAACA A G MRPL42 Ensembl:ENSG00000198015 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs778392078 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12097,RMVar_hsa_circ_26239,RMVar_hsa_circ_41575,RMVar_hsa_circ_316516,RMVar_hsa_circ_14974,RMVar_hsa_circ_332591,RMVar_hsa_circ_112019,RMVar_hsa_circ_158763,RMVar_hsa_circ_158764 29973 RMVar_ID_29973 Human_SNP_ID_511530990 A-to-I Human chr12 + 93476368 93476368 93476368 TTTTGTATTTTTAGTAGAGACAAAGTTTCACCATGTTAGTCAGGCTGGTCTCGAACTCCTTGACC TTTTGTATTTTTAGTAGAGACAAAGTTTCACCGTGTTAGTCAGGCTGGTCTCGAACTCCTTGACC A G MRPL42 Ensembl:ENSG00000198015 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1022634351 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12056519,Human_RBP_ID_25010058 RMVar_hsa_circ_12097,RMVar_hsa_circ_26239,RMVar_hsa_circ_41575,RMVar_hsa_circ_316516,RMVar_hsa_circ_14974,RMVar_hsa_circ_332591,RMVar_hsa_circ_112019,RMVar_hsa_circ_158763,RMVar_hsa_circ_158764 29974 RMVar_ID_29974 Human_SNP_ID_511537593 A-to-I Human chr12 + 93503398 93503397 93503398 CCAATAGCAAAAACTGATTTTTTTTTTTTTTTAAAGAAAAGGTCTTGCTGTGTCGCCCAGGATGG CCAATAGCAAAAACTGATTTTTTTTTTTTTTT_AAGAAAAGGTCTTGCTGTGTCGCCCAGGATGG TA T MRPL42 Ensembl:ENSG00000198015 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1174985441 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_430175,Human_RBP_ID_2362335,Human_RBP_ID_4244341,Human_RBP_ID_6233134,Human_RBP_ID_8179346,Human_RBP_ID_12057103,Human_RBP_ID_22384546,Human_RBP_ID_22795534,Human_RBP_ID_23159310,Human_RBP_ID_24407779,Human_RBP_ID_24468156,Human_RBP_ID_25028178,Human_RBP_ID_26421542,Human_RBP_ID_26912522 29975 RMVar_ID_29975 Human_SNP_ID_511537594 A-to-I Human chr12 + 93503398 93503398 93503398 CCAATAGCAAAAACTGATTTTTTTTTTTTTTTAAAGAAAAGGTCTTGCTGTGTCGCCCAGGATGG CCAATAGCAAAAACTGATTTTTTTTTTTTTTTGAAGAAAAGGTCTTGCTGTGTCGCCCAGGATGG A G MRPL42 Ensembl:ENSG00000198015 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1480098941 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_430175,Human_RBP_ID_2362335,Human_RBP_ID_4244341,Human_RBP_ID_6233134,Human_RBP_ID_8179346,Human_RBP_ID_12057103,Human_RBP_ID_22384546,Human_RBP_ID_22795534,Human_RBP_ID_23159310,Human_RBP_ID_24407779,Human_RBP_ID_24468156,Human_RBP_ID_25028178,Human_RBP_ID_26421542,Human_RBP_ID_26912522 29976 RMVar_ID_29976 Human_SNP_ID_511537612 A-to-I Human chr12 + 93503460 93503460 93503460 TGGAGTGCAGTGGCACAATCACATTGCACTGCAACCTCAATATCCTGGGCTCAAGCAATCCTCCC TGGAGTGCAGTGGCACAATCACATTGCACTGCCACCTCAATATCCTGGGCTCAAGCAATCCTCCC A C MRPL42 Ensembl:ENSG00000198015 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs919969307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_430176,Human_RBP_ID_6233139,Human_RBP_ID_12057105,Human_RBP_ID_17241064,Human_RBP_ID_17474316,Human_RBP_ID_17828909 29977 RMVar_ID_29977 Human_SNP_ID_511537799 A-to-I Human chr12 + 93504184 93504184 93504184 TTGGGTTTTGGAGATGGAGGTTTGCTCTGCCCAAGCTGGAATGCAATGGCGCGATCTTGGCTCAC TTGGGTTTTGGAGATGGAGGTTTGCTCTGCCCGAGCTGGAATGCAATGGCGCGATCTTGGCTCAC A G MRPL42 Ensembl:ENSG00000198015 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1422810689 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_995005,Human_RBP_ID_1478787,Human_RBP_ID_6233170,Human_RBP_ID_8786058,Human_RBP_ID_27634952 29978 RMVar_ID_29978 Human_SNP_ID_511537824 A-to-I Human chr12 + 93504271 93504271 93504271 CAAGTGATTCTCCTGCCTCAGCCTCCTTAAGTAGTTGGGATTACAAGTGTGCACCACCATACTCA CAAGTGATTCTCCTGCCTCAGCCTCCTTAAGTCGTTGGGATTACAAGTGTGCACCACCATACTCA A C MRPL42 Ensembl:ENSG00000198015 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs763294613 Functional Loss SNV dbSNP153 33..33 33 - - - 29979 RMVar_ID_29979 Human_SNP_ID_511537860 A-to-I Human chr12 + 93504383 93504383 93504383 GGCTGGTCTCGAACTCCTGACCTCAAGTGTCCACACACCTTGGCCTCCCAAAGTGCTGGGTGGGA GGCTGGTCTCGAACTCCTGACCTCAAGTGTCCCCACACCTTGGCCTCCCAAAGTGCTGGGTGGGA A C MRPL42 Ensembl:ENSG00000198015 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1483880774 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17828914,Human_RBP_ID_23159317 29980 RMVar_ID_29980 Human_SNP_ID_511539104 A-to-I Human chr12 + 93509534 93509534 93509534 ACATGCCTGTAGACCTAGCTACTCAGGAGGCTAAGACAGGAGGATCACTTGAGTCCAGAAGTTCT ACATGCCTGTAGACCTAGCTACTCAGGAGGCTGAGACAGGAGGATCACTTGAGTCCAGAAGTTCT A G MRPL42,RN7SL737P Ensembl:ENSG00000198015,Ensembl:ENSG00000243015 Protein coding,Other 3'UTR,exon GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs908246161 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8248773,Human_RBP_ID_12057334 29981 RMVar_ID_29981 Human_SNP_ID_511539108 A-to-I Human chr12 + 93509548 93509548 93509548 CTAGCTACTCAGGAGGCTAAGACAGGAGGATCACTTGAGTCCAGAAGTTCTGGGTTGTAGTGAGC CTAGCTACTCAGGAGGCTAAGACAGGAGGATCGCTTGAGTCCAGAAGTTCTGGGTTGTAGTGAGC A G MRPL42,RN7SL737P Ensembl:ENSG00000198015,Ensembl:ENSG00000243015 Protein coding,Other 3'UTR,exon GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1317779475 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8180037,Human_RBP_ID_8248773,Human_RBP_ID_12057336 29982 RMVar_ID_29982 Human_SNP_ID_511539682 A-to-I Human chr12 + 93512164 93512163 93512164 AAGCCAGTTTGGTCCCAGCTTTATAAAGATATACATTGGGCTGGGTGCGGTGGCTCATGCCTGTA AAGCCAGTTTGGTCCCAGCTTTATAAAGATAT_CATTGGGCTGGGTGCGGTGGCTCATGCCTGTA TA T MRPL42 Ensembl:ENSG00000198015 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355016623 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_17828961 29983 RMVar_ID_29983 Human_SNP_ID_511553209 A-to-I Human chr12 - 93569079 93569079 93569079 CTCACTGCAACCTCCGCCTCCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCGAGAAGCTGGG CTCACTGCAACCTCCGCCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGAAGCTGGG T C SOCS2-AS1 Ensembl:ENSG00000246985 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1271137741 Functional Loss SNV dbSNP153 33..33 33 - - - 29984 RMVar_ID_29984 Human_SNP_ID_511590566 A-to-I Human chr12 + 93729585 93729585 93729585 AAGGCGGGCAGATCACCTGAGGTTGGAGTTTGAGACCAGCCTGACCAACATGGAGAAACCCCATC AAGGCGGGCAGATCACCTGAGGTTGGAGTTTGCGACCAGCCTGACCAACATGGAGAAACCCCATC A C CRADD Ensembl:ENSG00000169372 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs371053205 Functional Loss SNV dbSNP153 33..33 33 - - - 29985 RMVar_ID_29985 Human_SNP_ID_511590570 A-to-I Human chr12 + 93729596 93729596 93729596 ATCACCTGAGGTTGGAGTTTGAGACCAGCCTGACCAACATGGAGAAACCCCATCTCTACTAAAAA ATCACCTGAGGTTGGAGTTTGAGACCAGCCTGGCCAACATGGAGAAACCCCATCTCTACTAAAAA A G CRADD Ensembl:ENSG00000169372 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1318793990 Functional Loss SNV dbSNP153 33..33 33 - - - 29986 RMVar_ID_29986 Human_SNP_ID_511727680 A-to-I Human chr12 - 94313459 94313459 94313459 ACAGTCATAGCTAACTGTAGCCTTGAACTCCTAGGCTTAATCCATCCTCCTGCCTCAGCCTCCCA ACAGTCATAGCTAACTGTAGCCTTGAACTCCTCGGCTTAATCCATCCTCCTGCCTCAGCCTCCCA T G CEP83 Ensembl:ENSG00000173588 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1266590495 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45738,RMVar_hsa_circ_89775,RMVar_hsa_circ_332671,RMVar_hsa_circ_354440,RMVar_hsa_circ_158800,RMVar_hsa_circ_336067,RMVar_hsa_circ_326320,RMVar_hsa_circ_158801,RMVar_hsa_circ_29915,RMVar_hsa_circ_284632,RMVar_hsa_circ_158802,RMVar_hsa_circ_158803,RMVar_hsa_circ_71167,RMVar_hsa_circ_106669,RMVar_hsa_circ_50470,RMVar_hsa_circ_158804 29987 RMVar_ID_29987 Human_SNP_ID_511731433 A-to-I Human chr12 - 94331208 94331208 94331208 TGGCTCACTGCAACCTCCATCCCCTGGGTTCAAGCGATTCTCATACCTCAGCCTTTCGAGTAGCT TGGCTCACTGCAACCTCCATCCCCTGGGTTCAGGCGATTCTCATACCTCAGCCTTTCGAGTAGCT T C CEP83 Ensembl:ENSG00000173588 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1380258266 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45738,RMVar_hsa_circ_89775,RMVar_hsa_circ_332671,RMVar_hsa_circ_354440,RMVar_hsa_circ_158800,RMVar_hsa_circ_336067,RMVar_hsa_circ_326320,RMVar_hsa_circ_158801,RMVar_hsa_circ_29915,RMVar_hsa_circ_284632,RMVar_hsa_circ_158802,RMVar_hsa_circ_158803,RMVar_hsa_circ_71167,RMVar_hsa_circ_106669,RMVar_hsa_circ_50470,RMVar_hsa_circ_158805,RMVar_hsa_circ_76701,RMVar_hsa_circ_107227,RMVar_hsa_circ_158804,RMVar_hsa_circ_158806 29988 RMVar_ID_29988 Human_SNP_ID_511738805 A-to-I Human chr12 - 94361853 94361853 94361853 CTACTAAAAATACAAAATTAGCTGGGCCTGGTAGTGTGCGCCAGTAATCCCAGCTACACTGGAGG CTACTAAAAATACAAAATTAGCTGGGCCTGGTGGTGTGCGCCAGTAATCCCAGCTACACTGGAGG T C CEP83 Ensembl:ENSG00000173588 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs374838996 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89775,RMVar_hsa_circ_332671,RMVar_hsa_circ_354440,RMVar_hsa_circ_158800,RMVar_hsa_circ_336067,RMVar_hsa_circ_158801,RMVar_hsa_circ_29915,RMVar_hsa_circ_158802,RMVar_hsa_circ_71167,RMVar_hsa_circ_50470,RMVar_hsa_circ_58189,RMVar_hsa_circ_107227,RMVar_hsa_circ_158806,RMVar_hsa_circ_341652,RMVar_hsa_circ_352567,RMVar_hsa_circ_61935,RMVar_hsa_circ_35292,RMVar_hsa_circ_70121,RMVar_hsa_circ_72243 29989 RMVar_ID_29989 Human_SNP_ID_511739427 A-to-I Human chr12 - 94364543 94364543 94364543 TCACTGTAACACTGAACTCCTGAGCTCAAGCAATCCTCCTGCCTCAGCCTCCCAAGTAGTTGGAA TCACTGTAACACTGAACTCCTGAGCTCAAGCAGTCCTCCTGCCTCAGCCTCCCAAGTAGTTGGAA T C CEP83 Ensembl:ENSG00000173588 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1021369999 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12059349 RMVar_hsa_circ_89775,RMVar_hsa_circ_332671,RMVar_hsa_circ_354440,RMVar_hsa_circ_158800,RMVar_hsa_circ_336067,RMVar_hsa_circ_158801,RMVar_hsa_circ_29915,RMVar_hsa_circ_158802,RMVar_hsa_circ_71167,RMVar_hsa_circ_50470,RMVar_hsa_circ_58189,RMVar_hsa_circ_107227,RMVar_hsa_circ_158806,RMVar_hsa_circ_341652,RMVar_hsa_circ_352567,RMVar_hsa_circ_61935,RMVar_hsa_circ_35292,RMVar_hsa_circ_70121,RMVar_hsa_circ_72243 29990 RMVar_ID_29990 Human_SNP_ID_511739431 A-to-I Human chr12 - 94364553 94364553 94364553 CGATCATGGCTCACTGTAACACTGAACTCCTGAGCTCAAGCAATCCTCCTGCCTCAGCCTCCCAA CGATCATGGCTCACTGTAACACTGAACTCCTGTGCTCAAGCAATCCTCCTGCCTCAGCCTCCCAA T A CEP83 Ensembl:ENSG00000173588 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005017367 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12059349 RMVar_hsa_circ_89775,RMVar_hsa_circ_332671,RMVar_hsa_circ_354440,RMVar_hsa_circ_158800,RMVar_hsa_circ_336067,RMVar_hsa_circ_158801,RMVar_hsa_circ_29915,RMVar_hsa_circ_158802,RMVar_hsa_circ_71167,RMVar_hsa_circ_50470,RMVar_hsa_circ_58189,RMVar_hsa_circ_107227,RMVar_hsa_circ_158806,RMVar_hsa_circ_341652,RMVar_hsa_circ_352567,RMVar_hsa_circ_61935,RMVar_hsa_circ_35292,RMVar_hsa_circ_70121,RMVar_hsa_circ_72243 29991 RMVar_ID_29991 Human_SNP_ID_511739432 A-to-I Human chr12 - 94364553 94364553 94364553 CGATCATGGCTCACTGTAACACTGAACTCCTGAGCTCAAGCAATCCTCCTGCCTCAGCCTCCCAA CGATCATGGCTCACTGTAACACTGAACTCCTGCGCTCAAGCAATCCTCCTGCCTCAGCCTCCCAA T G CEP83 Ensembl:ENSG00000173588 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005017367 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12059349 RMVar_hsa_circ_89775,RMVar_hsa_circ_332671,RMVar_hsa_circ_354440,RMVar_hsa_circ_158800,RMVar_hsa_circ_336067,RMVar_hsa_circ_158801,RMVar_hsa_circ_29915,RMVar_hsa_circ_158802,RMVar_hsa_circ_71167,RMVar_hsa_circ_50470,RMVar_hsa_circ_58189,RMVar_hsa_circ_107227,RMVar_hsa_circ_158806,RMVar_hsa_circ_341652,RMVar_hsa_circ_352567,RMVar_hsa_circ_61935,RMVar_hsa_circ_35292,RMVar_hsa_circ_70121,RMVar_hsa_circ_72243 29992 RMVar_ID_29992 Human_SNP_ID_511789509 A-to-I Human chr12 - 94577372 94577372 94577372 CATCCTGGCTAACAAGGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTAGCCAGGCGTGATG CATCCTGGCTAACAAGGTGAAACCCCGTCTCTGCTAAAAATACAAAAAATTAGCCAGGCGTGATG T C TMCC3 Ensembl:ENSG00000057704 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1156762052 Functional Loss SNV dbSNP153 33..33 33 - - - 29993 RMVar_ID_29993 Human_SNP_ID_511789516 A-to-I Human chr12 - 94577390 94577390 94577390 AGGTCAGGAGATTGAGACCATCCTGGCTAACAAGGTGAAACCCCGTCTCTACTAAAAATACAAAA AGGTCAGGAGATTGAGACCATCCTGGCTAACACGGTGAAACCCCGTCTCTACTAAAAATACAAAA T G TMCC3 Ensembl:ENSG00000057704 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs973573412 Functional Loss SNV dbSNP153 33..33 33 - - - 29994 RMVar_ID_29994 Human_SNP_ID_511890923 A-to-I Human chr12 - 95001597 95001597 95001597 TTGAGACAGGGTCTCGCTCTGTCACCCAGTCTAGAGTGCAGTGACTCGATCATGGCTCACTACAG TTGAGACAGGGTCTCGCTCTGTCACCCAGTCTGGAGTGCAGTGACTCGATCATGGCTCACTACAG T C NDUFA12 Ensembl:ENSG00000184752 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1279191710 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83213,RMVar_hsa_circ_111874,RMVar_hsa_circ_158821,RMVar_hsa_circ_158822 29995 RMVar_ID_29995 Human_SNP_ID_511891336 A-to-I Human chr12 - 95002762 95002762 95002762 AGTGGGGGAAGACAAATATGGAAACAAATACTATGAAGACAACAAGCAATTTTTTGGTGAGTGCA AGTGGGGGAAGACAAATATGGAAACAAATACTGTGAAGACAACAAGCAATTTTTTGGTGAGTGCA T C NDUFA12 Ensembl:ENSG00000184752 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs766118227 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1803201,Human_RBP_ID_3417162,Human_RBP_ID_17241928,Human_RBP_ID_17650807,Human_RBP_ID_18526834,Human_RBP_ID_19058840,Human_RBP_ID_27635103 Human_Splice_Rec_1408224,Human_Splice_Rec_1408225,Human_Splice_Rec_1408240,Human_Splice_Rec_1408246,Human_Splice_Rec_1408247,Human_Splice_Rec_1408254,Human_Splice_Rec_1408255,Human_Splice_Rec_1408260,Human_Splice_Rec_1408261,Human_Splice_Rec_1408264,Human_Splice_Rec_1408265 RMVar_hsa_circ_83213,RMVar_hsa_circ_111874,RMVar_hsa_circ_158821,RMVar_hsa_circ_158822 29996 RMVar_ID_29996 Human_SNP_ID_511891337 A-to-I Human chr12 - 95002762 95002762 95002762 AGTGGGGGAAGACAAATATGGAAACAAATACTATGAAGACAACAAGCAATTTTTTGGTGAGTGCA AGTGGGGGAAGACAAATATGGAAACAAATACTCTGAAGACAACAAGCAATTTTTTGGTGAGTGCA T G NDUFA12 Ensembl:ENSG00000184752 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs766118227 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1803201,Human_RBP_ID_3417162,Human_RBP_ID_17241928,Human_RBP_ID_17650807,Human_RBP_ID_18526834,Human_RBP_ID_19058840,Human_RBP_ID_27635103 Human_Splice_Rec_1408224,Human_Splice_Rec_1408225,Human_Splice_Rec_1408240,Human_Splice_Rec_1408246,Human_Splice_Rec_1408247,Human_Splice_Rec_1408254,Human_Splice_Rec_1408255,Human_Splice_Rec_1408260,Human_Splice_Rec_1408261,Human_Splice_Rec_1408264,Human_Splice_Rec_1408265 RMVar_hsa_circ_83213,RMVar_hsa_circ_111874,RMVar_hsa_circ_158821,RMVar_hsa_circ_158822 29997 RMVar_ID_29997 Human_SNP_ID_511897244 A-to-I Human chr12 - 95027260 95027260 95027260 GGTCAGGAGTTTGAGACCAGCCTGGGCAACATAATGAGACCTCTTCTCTACAAAAATCAAAACAG GGTCAGGAGTTTGAGACCAGCCTGGGCAACATGATGAGACCTCTTCTCTACAAAAATCAAAACAG T C NR2C1 Ensembl:ENSG00000120798 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1019884833 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12060839,Human_RBP_ID_25011343 RMVar_hsa_circ_52839,RMVar_hsa_circ_75813,RMVar_hsa_circ_311249,RMVar_hsa_circ_158823,RMVar_hsa_circ_328267,RMVar_hsa_circ_69512,RMVar_hsa_circ_5234 29998 RMVar_ID_29998 Human_SNP_ID_511897292 A-to-I Human chr12 - 95027492 95027492 95027492 CCTAAGGTGATCTACCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGAGTGAACCACCCGCCT CCTAAGGTGATCTACCCGCCTCGGCCTCCCAAGGTGCTGGGATTACAGGAGTGAACCACCCGCCT T C NR2C1 Ensembl:ENSG00000120798 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs932516832 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8385607 RMVar_hsa_circ_52839,RMVar_hsa_circ_75813,RMVar_hsa_circ_311249,RMVar_hsa_circ_158823,RMVar_hsa_circ_328267,RMVar_hsa_circ_69512,RMVar_hsa_circ_5234 29999 RMVar_ID_29999 Human_SNP_ID_511900649 A-to-I Human chr12 - 95041252 95041252 95041252 CGATCTCTCGACATCGTGATCCACCTGTCTCCACCTCCCAAAGTGCTGGGATTATAGGCACGAGC CGATCTCTCGACATCGTGATCCACCTGTCTCCGCCTCCCAAAGTGCTGGGATTATAGGCACGAGC T C NR2C1 Ensembl:ENSG00000120798 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs959148128 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69512,RMVar_hsa_circ_158824,RMVar_hsa_circ_317953,RMVar_hsa_circ_357612,RMVar_hsa_circ_5234,RMVar_hsa_circ_329433,RMVar_hsa_circ_127920,RMVar_hsa_circ_287903,RMVar_hsa_circ_55825,RMVar_hsa_circ_158826,RMVar_hsa_circ_158828,RMVar_hsa_circ_158829,RMVar_hsa_circ_158827,RMVar_hsa_circ_158825,RMVar_hsa_circ_73098,RMVar_hsa_circ_158831,RMVar_hsa_circ_295376,RMVar_hsa_circ_19785,RMVar_hsa_circ_348875,RMVar_hsa_circ_362276,RMVar_hsa_circ_295796,RMVar_hsa_circ_158832,RMVar_hsa_circ_158833,RMVar_hsa_circ_158834 30000 RMVar_ID_30000 Human_SNP_ID_511904094 A-to-I Human chr12 - 95054503 95054503 95054503 GGCTAGGAATTTGAGACCAACCTGGGAAACATAGCGAGACTCTGTCTCTAAAAATAAAAAAATTA GGCTAGGAATTTGAGACCAACCTGGGAAACATGGCGAGACTCTGTCTCTAAAAATAAAAAAATTA T C NR2C1 Ensembl:ENSG00000120798 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs533652270 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16868,RMVar_hsa_circ_69512,RMVar_hsa_circ_357612,RMVar_hsa_circ_127920,RMVar_hsa_circ_287903,RMVar_hsa_circ_55825,RMVar_hsa_circ_158826,RMVar_hsa_circ_158828,RMVar_hsa_circ_158829,RMVar_hsa_circ_158827,RMVar_hsa_circ_73098,RMVar_hsa_circ_158831,RMVar_hsa_circ_295376,RMVar_hsa_circ_362276,RMVar_hsa_circ_158832,RMVar_hsa_circ_41785,RMVar_hsa_circ_366929,RMVar_hsa_circ_40114 30001 RMVar_ID_30001 Human_SNP_ID_511904559 A-to-I Human chr12 - 95056243 95056243 95056243 GTTTTTTAAACAGGGTCCCCTCTTGTCACCCAAGCTGGGGGTACGGTGGTGGCACAGTAATGGCT GTTTTTTAAACAGGGTCCCCTCTTGTCACCCAGGCTGGGGGTACGGTGGTGGCACAGTAATGGCT T C NR2C1 Ensembl:ENSG00000120798 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs910142581 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6234950,Human_RBP_ID_12061386 RMVar_hsa_circ_16868,RMVar_hsa_circ_69512,RMVar_hsa_circ_357612,RMVar_hsa_circ_127920,RMVar_hsa_circ_287903,RMVar_hsa_circ_55825,RMVar_hsa_circ_158826,RMVar_hsa_circ_158828,RMVar_hsa_circ_158829,RMVar_hsa_circ_158827,RMVar_hsa_circ_73098,RMVar_hsa_circ_158831,RMVar_hsa_circ_295376,RMVar_hsa_circ_362276,RMVar_hsa_circ_158832,RMVar_hsa_circ_41785,RMVar_hsa_circ_366929,RMVar_hsa_circ_40114 30002 RMVar_ID_30002 Human_SNP_ID_511904754 A-to-I Human chr12 - 95056913 95056913 95056913 ACTCTGTTGCCGAGGCTAGAGTGCAGTGGCACAGTCTCGGCTCACTGCAAGCTCCGCTTCCCGGG ACTCTGTTGCCGAGGCTAGAGTGCAGTGGCACGGTCTCGGCTCACTGCAAGCTCCGCTTCCCGGG T C NR2C1 Ensembl:ENSG00000120798 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1250978559 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16868,RMVar_hsa_circ_69512,RMVar_hsa_circ_357612,RMVar_hsa_circ_127920,RMVar_hsa_circ_287903,RMVar_hsa_circ_55825,RMVar_hsa_circ_158826,RMVar_hsa_circ_158828,RMVar_hsa_circ_158829,RMVar_hsa_circ_158827,RMVar_hsa_circ_73098,RMVar_hsa_circ_158831,RMVar_hsa_circ_295376,RMVar_hsa_circ_362276,RMVar_hsa_circ_158832,RMVar_hsa_circ_41785,RMVar_hsa_circ_366929,RMVar_hsa_circ_40114 30003 RMVar_ID_30003 Human_SNP_ID_511905264 A-to-I Human chr12 - 95058692 95058692 95058692 TCGAGACTGCAGTGAACTGTGATCGCACCATTACACTTCAGCCTGGGCCACAGAGCGAGATCCCG TCGAGACTGCAGTGAACTGTGATCGCACCATTGCACTTCAGCCTGGGCCACAGAGCGAGATCCCG T C NR2C1 Ensembl:ENSG00000120798 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs888047447 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16868,RMVar_hsa_circ_127920,RMVar_hsa_circ_158829,RMVar_hsa_circ_73098,RMVar_hsa_circ_41785,RMVar_hsa_circ_49338,RMVar_hsa_circ_338821,RMVar_hsa_circ_158837 30004 RMVar_ID_30004 Human_SNP_ID_511931688 A-to-I Human chr12 - 95161036 95161036 95161036 AGCTGGGATTACGGGTGTGTGCCACCATGCCCAGCTAATTTTTGTATTTTTGGTGGAGACGGGGT AGCTGGGATTACGGGTGTGTGCCACCATGCCCGGCTAATTTTTGTATTTTTGGTGGAGACGGGGT T C FGD6 Ensembl:ENSG00000180263 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1281706203 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104286,RMVar_hsa_circ_158843,RMVar_hsa_circ_118506,RMVar_hsa_circ_158844,RMVar_hsa_circ_158845,RMVar_hsa_circ_117857,RMVar_hsa_circ_158846,RMVar_hsa_circ_84766,RMVar_hsa_circ_366339,RMVar_hsa_circ_121054,RMVar_hsa_circ_110946,RMVar_hsa_circ_77634,RMVar_hsa_circ_124878,RMVar_hsa_circ_158847,RMVar_hsa_circ_158852,RMVar_hsa_circ_106288,RMVar_hsa_circ_158853,RMVar_hsa_circ_158854,RMVar_hsa_circ_64691,RMVar_hsa_circ_158856,RMVar_hsa_circ_365789,RMVar_hsa_circ_108945,RMVar_hsa_circ_158859,RMVar_hsa_circ_158861,RMVar_hsa_circ_106762,RMVar_hsa_circ_158862,RMVar_hsa_circ_371134 30005 RMVar_ID_30005 Human_SNP_ID_511947768 A-to-I Human chr12 + 95227254 95227254 95227254 ACAATCACTGTTCACTGCAGCCTCCACTTCCCAGGCTCAGGTGATTATCTCATCTCAGCCTCCCA ACAATCACTGTTCACTGCAGCCTCCACTTCCCCGGCTCAGGTGATTATCTCATCTCAGCCTCCCA A C VEZT Ensembl:ENSG00000028203 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs561044410 Functional Loss SNV dbSNP153 33..33 33 - - - 30006 RMVar_ID_30006 Human_SNP_ID_511958817 A-to-I Human chr12 + 95274310 95274310 95274310 AACATGGCAAAACATCATCTCTAGAAAAAAATACAAAAATCAGCTGGGTGTGGTGGCGCATGCCT AACATGGCAAAACATCATCTCTAGAAAAAAATGCAAAAATCAGCTGGGTGTGGTGGCGCATGCCT A G VEZT Ensembl:ENSG00000028203 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs979651932 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70131,RMVar_hsa_circ_355152,RMVar_hsa_circ_287708,RMVar_hsa_circ_325604,RMVar_hsa_circ_326632,RMVar_hsa_circ_328764,RMVar_hsa_circ_275894,RMVar_hsa_circ_34661,RMVar_hsa_circ_10464,RMVar_hsa_circ_158871,RMVar_hsa_circ_158873,RMVar_hsa_circ_158872,RMVar_hsa_circ_158878,RMVar_hsa_circ_288101,RMVar_hsa_circ_279585,RMVar_hsa_circ_50102,RMVar_hsa_circ_302802,RMVar_hsa_circ_50453,RMVar_hsa_circ_27894,RMVar_hsa_circ_158879,RMVar_hsa_circ_45896,RMVar_hsa_circ_310029,RMVar_hsa_circ_280728,RMVar_hsa_circ_103222,RMVar_hsa_circ_55481,RMVar_hsa_circ_158885,RMVar_hsa_circ_158889,RMVar_hsa_circ_279573,RMVar_hsa_circ_158880,RMVar_hsa_circ_158882,RMVar_hsa_circ_158881,RMVar_hsa_circ_285365,RMVar_hsa_circ_283384,RMVar_hsa_circ_44660,RMVar_hsa_circ_270360,RMVar_hsa_circ_158890,RMVar_hsa_circ_158887,RMVar_hsa_circ_158888,RMVar_hsa_circ_158886,RMVar_hsa_circ_158892,RMVar_hsa_circ_278128,RMVar_hsa_circ_309462,RMVar_hsa_circ_355704,RMVar_hsa_circ_295133,RMVar_hsa_circ_158893,RMVar_hsa_circ_321497,RMVar_hsa_circ_336748,RMVar_hsa_circ_158891,RMVar_hsa_circ_333751,RMVar_hsa_circ_318321,RMVar_hsa_circ_158894 30007 RMVar_ID_30007 Human_SNP_ID_511958830 A-to-I Human chr12 + 95274355 95274355 95274355 GGGTGTGGTGGCGCATGCCTGTAATCCCAGCTACTCGAGAGGCTGAGACATGAGAATTGCTTGAA GGGTGTGGTGGCGCATGCCTGTAATCCCAGCTGCTCGAGAGGCTGAGACATGAGAATTGCTTGAA A G VEZT Ensembl:ENSG00000028203 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1186809927 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70131,RMVar_hsa_circ_355152,RMVar_hsa_circ_287708,RMVar_hsa_circ_325604,RMVar_hsa_circ_326632,RMVar_hsa_circ_328764,RMVar_hsa_circ_275894,RMVar_hsa_circ_34661,RMVar_hsa_circ_10464,RMVar_hsa_circ_158871,RMVar_hsa_circ_158873,RMVar_hsa_circ_158872,RMVar_hsa_circ_158878,RMVar_hsa_circ_288101,RMVar_hsa_circ_279585,RMVar_hsa_circ_50102,RMVar_hsa_circ_302802,RMVar_hsa_circ_50453,RMVar_hsa_circ_27894,RMVar_hsa_circ_158879,RMVar_hsa_circ_45896,RMVar_hsa_circ_310029,RMVar_hsa_circ_280728,RMVar_hsa_circ_103222,RMVar_hsa_circ_55481,RMVar_hsa_circ_158885,RMVar_hsa_circ_158889,RMVar_hsa_circ_279573,RMVar_hsa_circ_158880,RMVar_hsa_circ_158882,RMVar_hsa_circ_158881,RMVar_hsa_circ_285365,RMVar_hsa_circ_283384,RMVar_hsa_circ_44660,RMVar_hsa_circ_270360,RMVar_hsa_circ_158890,RMVar_hsa_circ_158887,RMVar_hsa_circ_158888,RMVar_hsa_circ_158886,RMVar_hsa_circ_158892,RMVar_hsa_circ_278128,RMVar_hsa_circ_309462,RMVar_hsa_circ_355704,RMVar_hsa_circ_295133,RMVar_hsa_circ_158893,RMVar_hsa_circ_321497,RMVar_hsa_circ_336748,RMVar_hsa_circ_158891,RMVar_hsa_circ_333751,RMVar_hsa_circ_318321,RMVar_hsa_circ_158894 30008 RMVar_ID_30008 Human_SNP_ID_512011053 A-to-I Human chr12 + 95481272 95481270 95481272 CTCTGCAAAAGATTAAAAAACATTAGCCAGGTATAGTGGTGCGTGCCTGTAGTCTCAGCTATTCA CTCTGCAAAAGATTAAAAAACATTAGCCAGG__TAGTGGTGCGTGCCTGTAGTCTCAGCTATTCA GTA G METAP2 Ensembl:ENSG00000111142 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs933485321 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_4792,RMVar_hsa_circ_366669,RMVar_hsa_circ_66936,RMVar_hsa_circ_158901,RMVar_hsa_circ_158902,RMVar_hsa_circ_32493 30009 RMVar_ID_30009 Human_SNP_ID_512011055 A-to-I Human chr12 + 95481272 95481272 95481272 CTCTGCAAAAGATTAAAAAACATTAGCCAGGTATAGTGGTGCGTGCCTGTAGTCTCAGCTATTCA CTCTGCAAAAGATTAAAAAACATTAGCCAGGTGTAGTGGTGCGTGCCTGTAGTCTCAGCTATTCA A G METAP2 Ensembl:ENSG00000111142 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs747697210 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4792,RMVar_hsa_circ_366669,RMVar_hsa_circ_66936,RMVar_hsa_circ_158901,RMVar_hsa_circ_158902,RMVar_hsa_circ_32493 30010 RMVar_ID_30010 Human_SNP_ID_512011056 A-to-I Human chr12 + 95481274 95481274 95481274 CTGCAAAAGATTAAAAAACATTAGCCAGGTATAGTGGTGCGTGCCTGTAGTCTCAGCTATTCAGG CTGCAAAAGATTAAAAAACATTAGCCAGGTATGGTGGTGCGTGCCTGTAGTCTCAGCTATTCAGG A G METAP2 Ensembl:ENSG00000111142 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs888900313 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4792,RMVar_hsa_circ_366669,RMVar_hsa_circ_66936,RMVar_hsa_circ_158901,RMVar_hsa_circ_158902,RMVar_hsa_circ_32493 30011 RMVar_ID_30011 Human_SNP_ID_512011350 A-to-I Human chr12 + 95482522 95482522 95482522 GATTTTGAGGCTGGGTACAGTGGCTCACGCCTATAATCCCAGGACTTGGGAGGCCAAGGCTGGCA GATTTTGAGGCTGGGTACAGTGGCTCACGCCTGTAATCCCAGGACTTGGGAGGCCAAGGCTGGCA A G METAP2 Ensembl:ENSG00000111142 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs561253278 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17561233,Human_RBP_ID_25012440 RMVar_hsa_circ_4792,RMVar_hsa_circ_366669,RMVar_hsa_circ_66936,RMVar_hsa_circ_158901,RMVar_hsa_circ_158902,RMVar_hsa_circ_32493 30012 RMVar_ID_30012 Human_SNP_ID_512012441 A-to-I Human chr12 + 95486731 95486731 95486731 GTGGATCAGGCTGGTCTTGAACTCCCAACCTCAGGTGATCCGCCCACCTTGGCCTCCCAAAGTGC GTGGATCAGGCTGGTCTTGAACTCCCAACCTCCGGTGATCCGCCCACCTTGGCCTCCCAAAGTGC A C METAP2 Ensembl:ENSG00000111142 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1361739555 Functional Loss SNV dbSNP153 33..33 33 - - - 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 30013 RMVar_ID_30013 Human_SNP_ID_512012442 A-to-I Human chr12 + 95486731 95486731 95486731 GTGGATCAGGCTGGTCTTGAACTCCCAACCTCAGGTGATCCGCCCACCTTGGCCTCCCAAAGTGC GTGGATCAGGCTGGTCTTGAACTCCCAACCTCTGGTGATCCGCCCACCTTGGCCTCCCAAAGTGC A T METAP2 Ensembl:ENSG00000111142 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1361739555 Functional Loss SNV dbSNP153 33..33 33 - - - 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 30014 RMVar_ID_30014 Human_SNP_ID_512016068 A-to-I Human chr12 + 95501217 95501217 95501217 ATAAAATAATATTTTAAATTTTTTGTAGATACAGGGTCTTGCTGTCTTGCCCAGGCTGGTCTGGA ATAAAATAATATTTTAAATTTTTTGTAGATACCGGGTCTTGCTGTCTTGCCCAGGCTGGTCTGGA A C METAP2 Ensembl:ENSG00000111142 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042616552 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1938,RMVar_hsa_circ_4792,RMVar_hsa_circ_17588,RMVar_hsa_circ_158902,RMVar_hsa_circ_158903,RMVar_hsa_circ_32493,RMVar_hsa_circ_351610,RMVar_hsa_circ_284975,RMVar_hsa_circ_268859,RMVar_hsa_circ_333010,RMVar_hsa_circ_158904,RMVar_hsa_circ_306089,RMVar_hsa_circ_158906 30015 RMVar_ID_30015 Human_SNP_ID_512017373 A-to-I Human chr12 + 95506054 95506054 95506054 AGGAGGCAGAGGTTGCAGTGAGTCAAGATTGCACCATTGCACTCCAGCCTGGGCGACAGAGTGAG AGGAGGCAGAGGTTGCAGTGAGTCAAGATTGCGCCATTGCACTCCAGCCTGGGCGACAGAGTGAG A G METAP2 Ensembl:ENSG00000111142 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs55731454 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25012677 RMVar_hsa_circ_1938,RMVar_hsa_circ_17588,RMVar_hsa_circ_268859,RMVar_hsa_circ_333010,RMVar_hsa_circ_12639,RMVar_hsa_circ_119507,RMVar_hsa_circ_158907 30016 RMVar_ID_30016 Human_SNP_ID_512017435 A-to-I Human chr12 + 95506221 95506221 95506221 GAGTGCGCTCAGCTTCCCGAGTAGCTGGGACTACAGATGTACAGTATCATACCTGGCTAATTTTT GAGTGCGCTCAGCTTCCCGAGTAGCTGGGACTGCAGATGTACAGTATCATACCTGGCTAATTTTT A G METAP2 Ensembl:ENSG00000111142 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1176387986 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1938,RMVar_hsa_circ_17588,RMVar_hsa_circ_268859,RMVar_hsa_circ_333010,RMVar_hsa_circ_12639,RMVar_hsa_circ_119507,RMVar_hsa_circ_158907 30017 RMVar_ID_30017 Human_SNP_ID_512107091 A-to-I Human chr12 + 95876081 95876081 95876081 TGTCCATCAACAGATGAATGAATAAACAATATATGGTATAAACATACAATGGAATATTATCTAGC TGTCCATCAACAGATGAATGAATAAACAATATGTGGTATAAACATACAATGGAATATTATCTAGC A G SNRPF Ensembl:ENSG00000139343 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs997085509 Functional Loss SNV dbSNP153 33..33 33 - - - 30018 RMVar_ID_30018 Human_SNP_ID_512107092 A-to-I Human chr12 + 95876086 95876086 95876086 ATCAACAGATGAATGAATAAACAATATATGGTATAAACATACAATGGAATATTATCTAGCTGTAA ATCAACAGATGAATGAATAAACAATATATGGTGTAAACATACAATGGAATATTATCTAGCTGTAA A G SNRPF Ensembl:ENSG00000139343 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1028208535 Functional Loss SNV dbSNP153 33..33 33 - - - 30019 RMVar_ID_30019 Human_SNP_ID_512133867 A-to-I Human chr12 - 95981716 95981716 95981716 GTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGCTGATCACTTGAGGCCAAGA GTGGCTCACACCTGTAATCCCAGCACTTTGGGGGGCCAAGGTGGGCTGATCACTTGAGGCCAAGA T C HAL Ensembl:ENSG00000084110 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1294442032 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56340,RMVar_hsa_circ_111121,RMVar_hsa_circ_158927,RMVar_hsa_circ_358173,RMVar_hsa_circ_68071 30020 RMVar_ID_30020 Human_SNP_ID_512204292 A-to-I Human chr12 - 96264282 96264282 96264282 CTTCAATATTTGTAGTATCATTTCCTCTAGCCAGGTATGGTCGTTGACACCTGTAATCCTAGCCC CTTCAATATTTGTAGTATCATTTCCTCTAGCCTGGTATGGTCGTTGACACCTGTAATCCTAGCCC T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048473638 Functional Loss SNV dbSNP153 33..33 33 - - - 30021 RMVar_ID_30021 Human_SNP_ID_512204373 A-to-I Human chr12 - 96264617 96264617 96264617 GCACACGTGGCCAATTTTTGTATTTTTTTTGGAGAGACAGGGTCTTGCTATGTTGCCCCTGATGG GCACACGTGGCCAATTTTTGTATTTTTTTTGGGGAGACAGGGTCTTGCTATGTTGCCCCTGATGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991207412 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12065122 30022 RMVar_ID_30022 Human_SNP_ID_512206012 A-to-I Human chr12 - 96270757 96270757 96270757 ATGATCTCGGCTCACTGCAACCTCCACCTCCCAGATCCAGGTGATTCTCCTGCCTCAGCCTCCCG ATGATCTCGGCTCACTGCAACCTCCACCTCCCCGATCCAGGTGATTCTCCTGCCTCAGCCTCCCG T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs995671643 Functional Loss SNV dbSNP153 33..33 33 - - - 30023 RMVar_ID_30023 Human_SNP_ID_512215874 A-to-I Human chr12 - 96311097 96311097 96311097 GGATATCTTGAAAAGTTGCAGATAAACAGTCCACCATTTGACCAACCAATGAGTCGAAGGTCTCG GGATATCTTGAAAAGTTGCAGATAAACAGTCCTCCATTTGACCAACCAATGAGTCGAAGGTCTCG T A CDK17 Ensembl:ENSG00000059758 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017918832 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1410100,Human_Splice_Rec_1410101,Human_Splice_Rec_1410132,Human_Splice_Rec_1410133,Human_Splice_Rec_1410160,Human_Splice_Rec_1410161,Human_Splice_Rec_1410220,Human_Splice_Rec_1410228 Human_miRNA_ID_47639,Human_miRNA_ID_644575,Human_miRNA_ID_1656739,Human_miRNA_ID_1980865,Human_miRNA_ID_1982589,Human_miRNA_ID_2247330,Human_miRNA_ID_2851641 RMVar_hsa_circ_366110,RMVar_hsa_circ_354617,RMVar_hsa_circ_70996,RMVar_hsa_circ_8640,RMVar_hsa_circ_71837,RMVar_hsa_circ_18922,RMVar_hsa_circ_34107,RMVar_hsa_circ_368995,RMVar_hsa_circ_319232,RMVar_hsa_circ_65177,RMVar_hsa_circ_158947,RMVar_hsa_circ_158948,RMVar_hsa_circ_53559,RMVar_hsa_circ_307268,RMVar_hsa_circ_158950,RMVar_hsa_circ_23157,RMVar_hsa_circ_357302,RMVar_hsa_circ_158953,RMVar_hsa_circ_78798,RMVar_hsa_circ_340504,RMVar_hsa_circ_158951,RMVar_hsa_circ_276226,RMVar_hsa_circ_23497,RMVar_hsa_circ_158954,RMVar_hsa_circ_158952 30024 RMVar_ID_30024 Human_SNP_ID_512227409 A-to-I Human chr12 - 96356405 96356405 96356405 GTAAGTCCCAGCGACTTGGGGGGCTGAGGCAAAAGGATTGCTTGAGCCTGGGCAACAGAGGCTTC GTAAGTCCCAGCGACTTGGGGGGCTGAGGCAACAGGATTGCTTGAGCCTGGGCAACAGAGGCTTC T G CDK17 Ensembl:ENSG00000059758 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1400384997 Functional Loss SNV dbSNP153 33..33 33 - - - 30025 RMVar_ID_30025 Human_SNP_ID_512227610 A-to-I Human chr12 - 96357346 96357346 96357346 GCGATTCTCCTGCCTCAGCTTCCTAAGTAGCTAGGACTACAGGCACATGACACCACATCTGGCTA GCGATTCTCCTGCCTCAGCTTCCTAAGTAGCTGGGACTACAGGCACATGACACCACATCTGGCTA T C CDK17 Ensembl:ENSG00000059758 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017729040 Functional Loss SNV dbSNP153 33..33 33 - - - 30026 RMVar_ID_30026 Human_SNP_ID_512233290 A-to-I Human chr12 - 96380047 96380047 96380047 CTCCCACCTCAGCCTCCATAGTAGCTGGGACTACAGGTGTGTGCCACCATGCACAGCTAATTTTT CTCCCACCTCAGCCTCCATAGTAGCTGGGACTGCAGGTGTGTGCCACCATGCACAGCTAATTTTT T C CDK17 Ensembl:ENSG00000059758 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1273955691 Functional Loss SNV dbSNP153 33..33 33 - - - 30027 RMVar_ID_30027 Human_SNP_ID_512234999 A-to-I Human chr12 - 96386431 96386431 96386431 TTTTGCAGGCTGGTCTCAAACTTCTGGGCTCAAGTGATCCTCCCACCTTGGCCTCCCAAAGTGCC TTTTGCAGGCTGGTCTCAAACTTCTGGGCTCAGGTGATCCTCCCACCTTGGCCTCCCAAAGTGCC T C CDK17 Ensembl:ENSG00000059758 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs902453514 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17560912 30028 RMVar_ID_30028 Human_SNP_ID_512236154 A-to-I Human chr12 - 96391035 96391035 96391035 TCGTTTAGGTTGGAGTGCAGTGGTGCAATCTCAGCTCACTACAACCTCCACCTCCCGGGTTCAGT TCGTTTAGGTTGGAGTGCAGTGGTGCAATCTCTGCTCACTACAACCTCCACCTCCCGGGTTCAGT T A CDK17 Ensembl:ENSG00000059758 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1401481720 Functional Loss SNV dbSNP153 33..33 33 - - - 30029 RMVar_ID_30029 Human_SNP_ID_512236780 A-to-I Human chr12 - 96393329 96393329 96393329 TTTTTTTGAGGCGGAGCCTCACAGGCTGGAGTACAATGGCACAATCTTGGCTCACTGCAACCTCC TTTTTTTGAGGCGGAGCCTCACAGGCTGGAGTGCAATGGCACAATCTTGGCTCACTGCAACCTCC T C CDK17 Ensembl:ENSG00000059758 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs987375700 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6237166 30030 RMVar_ID_30030 Human_SNP_ID_512761025 A-to-I Human chr12 + 98521372 98521372 98521372 CTGATCTTCTGATCCTCCCGCCTCAGCCTCCCAGAGTGCTGGGATTACAGACGTGAGCCACCGTG CTGATCTTCTGATCCTCCCGCCTCAGCCTCCCTGAGTGCTGGGATTACAGACGTGAGCCACCGTG A T TMPO Ensembl:ENSG00000120802 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1292893118 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103003,RMVar_hsa_circ_159015 30031 RMVar_ID_30031 Human_SNP_ID_512761171 A-to-I Human chr12 + 98521895 98521895 98521895 GGGATTACAAGCGTGCACCACCATGCCCAGCTAATTTTTTTATTTTTAGTAGAGACAGTTTCACC GGGATTACAAGCGTGCACCACCATGCCCAGCTGATTTTTTTATTTTTAGTAGAGACAGTTTCACC A G TMPO Ensembl:ENSG00000120802 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1333821800 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12067793 RMVar_hsa_circ_103003,RMVar_hsa_circ_159015 30032 RMVar_ID_30032 Human_SNP_ID_512761173 A-to-I Human chr12 + 98521904 98521904 98521904 AGCGTGCACCACCATGCCCAGCTAATTTTTTTATTTTTAGTAGAGACAGTTTCACCATGTTGGTC AGCGTGCACCACCATGCCCAGCTAATTTTTTTGTTTTTAGTAGAGACAGTTTCACCATGTTGGTC A G TMPO Ensembl:ENSG00000120802 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1398044868 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12067793 RMVar_hsa_circ_103003,RMVar_hsa_circ_159015 30033 RMVar_ID_30033 Human_SNP_ID_512761662 A-to-I Human chr12 + 98523739 98523739 98523739 GCCTTATCACCCAGGCTGGAGTGCAGTGGCGCAATCTTGGCTCGCTGCAATCTCCGCCTCCCCAA GCCTTATCACCCAGGCTGGAGTGCAGTGGCGCGATCTTGGCTCGCTGCAATCTCCGCCTCCCCAA A G TMPO Ensembl:ENSG00000120802 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs550594400 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103003,RMVar_hsa_circ_159015 30034 RMVar_ID_30034 Human_SNP_ID_512761698 A-to-I Human chr12 + 98523841 98523841 98523841 AGGACTATAGGCGTGTGCCATCACACCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCA AGGACTATAGGCGTGTGCCATCACACCTGGCTCATTTTTGTATTTTTAGTAGAGATGGGGTTTCA A C TMPO Ensembl:ENSG00000120802 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1314972342 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103003,RMVar_hsa_circ_159015 30035 RMVar_ID_30035 Human_SNP_ID_512761737 A-to-I Human chr12 + 98523947 98523947 98523947 GAGATCCTCCCTCCTCGGCCTCCCAAAGTGCTAGAATTACAGACATGAGCCACTGCCGAGAATTG GAGATCCTCCCTCCTCGGCCTCCCAAAGTGCTGGAATTACAGACATGAGCCACTGCCGAGAATTG A G TMPO Ensembl:ENSG00000120802 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs115559506 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12067849 RMVar_hsa_circ_103003,RMVar_hsa_circ_159015 30036 RMVar_ID_30036 Human_SNP_ID_512761947 A-to-I Human chr12 + 98524759 98524759 98524759 GGGATTACAGGCATGTGCCACCACACCCGGCTAATTTTTGCATTTTTAAAAGAGACGGGGTTTCA GGGATTACAGGCATGTGCCACCACACCCGGCTCATTTTTGCATTTTTAAAAGAGACGGGGTTTCA A C TMPO Ensembl:ENSG00000120802 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs974308939 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103003,RMVar_hsa_circ_159015 30037 RMVar_ID_30037 Human_SNP_ID_512761957 A-to-I Human chr12 + 98524791 98524791 98524791 AATTTTTGCATTTTTAAAAGAGACGGGGTTTCACCGTGTTGGCCATGCTGGTCTCGAACTCCTGA AATTTTTGCATTTTTAAAAGAGACGGGGTTTCCCCGTGTTGGCCATGCTGGTCTCGAACTCCTGA A C TMPO Ensembl:ENSG00000120802 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs749462713 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103003,RMVar_hsa_circ_159015 30038 RMVar_ID_30038 Human_SNP_ID_512761958 A-to-I Human chr12 + 98524791 98524791 98524791 AATTTTTGCATTTTTAAAAGAGACGGGGTTTCACCGTGTTGGCCATGCTGGTCTCGAACTCCTGA AATTTTTGCATTTTTAAAAGAGACGGGGTTTCGCCGTGTTGGCCATGCTGGTCTCGAACTCCTGA A G TMPO Ensembl:ENSG00000120802 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs749462713 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103003,RMVar_hsa_circ_159015 30039 RMVar_ID_30039 Human_SNP_ID_512762158 A-to-I Human chr12 + 98525620 98525619 98525620 AAAATTAGCCGGGCGTGGTGGTGCACACCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA AAAATTAGCCGGGCGTGGTGGTGCACACCTGT_ATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA TA T TMPO Ensembl:ENSG00000120802 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs995534369 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_103003,RMVar_hsa_circ_159015 30040 RMVar_ID_30040 Human_SNP_ID_512762159 A-to-I Human chr12 + 98525620 98525620 98525620 AAAATTAGCCGGGCGTGGTGGTGCACACCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA AAAATTAGCCGGGCGTGGTGGTGCACACCTGTGATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA A G TMPO Ensembl:ENSG00000120802 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1025893438 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103003,RMVar_hsa_circ_159015 30041 RMVar_ID_30041 Human_SNP_ID_512766149 A-to-I Human chr12 + 98538536 98538536 98538536 CACCACGCTCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCGTGTTGGCCAGGCTGG CACCACGCTCAGCTAATTTTTGTATTTTTAGTGGAGACGGGGTTTCACCGTGTTGGCCAGGCTGG A G TMPO Ensembl:ENSG00000120802 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1015590230 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_62400,RMVar_hsa_circ_305831,RMVar_hsa_circ_62585,RMVar_hsa_circ_341395,RMVar_hsa_circ_30109 30042 RMVar_ID_30042 Human_SNP_ID_512766515 A-to-I Human chr12 + 98539748 98539748 98539748 CACCCGCCTTGGCCTCCCAGATTGCTGGGATTACAGGCATGAGCTACCGCACCTGGCAATAAATT CACCCGCCTTGGCCTCCCAGATTGCTGGGATTGCAGGCATGAGCTACCGCACCTGGCAATAAATT A G TMPO Ensembl:ENSG00000120802 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1310006556 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23159448 RMVar_hsa_circ_62400,RMVar_hsa_circ_305831,RMVar_hsa_circ_62585,RMVar_hsa_circ_341395,RMVar_hsa_circ_30109 30043 RMVar_ID_30043 Human_SNP_ID_512766721 A-to-I Human chr12 + 98540508 98540508 98540508 TCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCATGTGCCACCACGCCCG TCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTTGCTGGGATTACAGGCATGTGCCACCACGCCCG A T TMPO Ensembl:ENSG00000120802 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1378350764 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_62400,RMVar_hsa_circ_305831,RMVar_hsa_circ_62585,RMVar_hsa_circ_341395,RMVar_hsa_circ_30109 30044 RMVar_ID_30044 Human_SNP_ID_512767273 A-to-I Human chr12 + 98542747 98542747 98542747 AAGTGTGCTGGTGCGTGCCTGTAATCCCAGCTACTCAGGAGGGTGAGGCAGGAGAATCACTTGAA AAGTGTGCTGGTGCGTGCCTGTAATCCCAGCTGCTCAGGAGGGTGAGGCAGGAGAATCACTTGAA A G TMPO Ensembl:ENSG00000120802 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1316094873 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22178413 RMVar_hsa_circ_62400,RMVar_hsa_circ_305831,RMVar_hsa_circ_62585,RMVar_hsa_circ_341395,RMVar_hsa_circ_30109 30045 RMVar_ID_30045 Human_SNP_ID_512767274 A-to-I Human chr12 + 98542751 98542751 98542751 GTGCTGGTGCGTGCCTGTAATCCCAGCTACTCAGGAGGGTGAGGCAGGAGAATCACTTGAACCTC GTGCTGGTGCGTGCCTGTAATCCCAGCTACTCCGGAGGGTGAGGCAGGAGAATCACTTGAACCTC A C TMPO Ensembl:ENSG00000120802 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1023615833 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22178413 RMVar_hsa_circ_62400,RMVar_hsa_circ_305831,RMVar_hsa_circ_62585,RMVar_hsa_circ_341395,RMVar_hsa_circ_30109 30046 RMVar_ID_30046 Human_SNP_ID_512767275 A-to-I Human chr12 + 98542751 98542751 98542751 GTGCTGGTGCGTGCCTGTAATCCCAGCTACTCAGGAGGGTGAGGCAGGAGAATCACTTGAACCTC GTGCTGGTGCGTGCCTGTAATCCCAGCTACTCGGGAGGGTGAGGCAGGAGAATCACTTGAACCTC A G TMPO Ensembl:ENSG00000120802 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1023615833 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22178413 RMVar_hsa_circ_62400,RMVar_hsa_circ_305831,RMVar_hsa_circ_62585,RMVar_hsa_circ_341395,RMVar_hsa_circ_30109 30047 RMVar_ID_30047 Human_SNP_ID_512769006 A-to-I Human chr12 + 98549000 98549000 98549000 AAAATTAGCTGGGCGTGATGATGTGCGCCTGTAGTCCTGTCTACTAGGGAGACTGAGGCAGGAGA AAAATTAGCTGGGCGTGATGATGTGCGCCTGTGGTCCTGTCTACTAGGGAGACTGAGGCAGGAGA A G TMPO Ensembl:ENSG00000120802 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) 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 30048 RMVar_ID_30048 Human_SNP_ID_512769011 A-to-I Human chr12 + 98549027 98549027 98549027 CCTGTAGTCCTGTCTACTAGGGAGACTGAGGCAGGAGAATCGTTTGAACCCAGGAGGCAGAGGTT CCTGTAGTCCTGTCTACTAGGGAGACTGAGGCCGGAGAATCGTTTGAACCCAGGAGGCAGAGGTT A C TMPO Ensembl:ENSG00000120802 Protein coding 3'UTR GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs942547511 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3418070,Human_RBP_ID_26421546,Human_RBP_ID_27425735 30049 RMVar_ID_30049 Human_SNP_ID_512769017 A-to-I Human chr12 + 98549041 98549041 98549041 TACTAGGGAGACTGAGGCAGGAGAATCGTTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCAGAGA TACTAGGGAGACTGAGGCAGGAGAATCGTTTGGACCCAGGAGGCAGAGGTTGCAGTGAGCAGAGA A G TMPO Ensembl:ENSG00000120802 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1380312362 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25014605,Human_RBP_ID_26421546,Human_RBP_ID_27425735 30050 RMVar_ID_30050 Human_SNP_ID_512769023 A-to-I Human chr12 + 98549062 98549062 98549062 AGAATCGTTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCAGAGATTACGTCACTGCACTGTAGCC AGAATCGTTTGAACCCAGGAGGCAGAGGTTGCCGTGAGCAGAGATTACGTCACTGCACTGTAGCC A C TMPO Ensembl:ENSG00000120802 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs186285844 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9709997,Human_RBP_ID_12068726,Human_RBP_ID_18206478,Human_RBP_ID_25014607,Human_RBP_ID_26420848,Human_RBP_ID_27425735 30051 RMVar_ID_30051 Human_SNP_ID_512769026 A-to-I Human chr12 + 98549073 98549073 98549073 AACCCAGGAGGCAGAGGTTGCAGTGAGCAGAGATTACGTCACTGCACTGTAGCCTGGCGACAGAG AACCCAGGAGGCAGAGGTTGCAGTGAGCAGAGGTTACGTCACTGCACTGTAGCCTGGCGACAGAG A G TMPO Ensembl:ENSG00000120802 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs960962895 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9709997,Human_RBP_ID_12068726,Human_RBP_ID_17829945,Human_RBP_ID_18206478,Human_RBP_ID_25014607,Human_RBP_ID_26420848,Human_RBP_ID_27425736 30052 RMVar_ID_30052 Human_SNP_ID_512769036 A-to-I Human chr12 + 98549107 98549107 98549107 TACGTCACTGCACTGTAGCCTGGCGACAGAGCAAGACTCCATCTCAAAAAAAATAAAAAAGTACA TACGTCACTGCACTGTAGCCTGGCGACAGAGCGAGACTCCATCTCAAAAAAAATAAAAAAGTACA A G TMPO Ensembl:ENSG00000120802 Protein coding 3'UTR GSE38233;GSE100210;GSE100210;GSE99789;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;HepG2 cell line;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,29129909,29796672,29796672,31158229,31158229,31158229,31158229,31158229 RNA-Seq:(High) rs968204668 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23159472,Human_RBP_ID_26420849 30053 RMVar_ID_30053 Human_SNP_ID_512769078 A-to-I Human chr12 + 98549264 98549264 98549264 TATTTTTTATGAGATGGAGTCTCACTCTTGTCACCCAGACTGTAGTGCAGTGGCACGATCTGGGC TATTTTTTATGAGATGGAGTCTCACTCTTGTCCCCCAGACTGTAGTGCAGTGGCACGATCTGGGC A C TMPO Ensembl:ENSG00000120802 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1371125751 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12068733,Human_RBP_ID_17561240,Human_RBP_ID_17829951,Human_RBP_ID_23306343,Human_RBP_ID_26420853 30054 RMVar_ID_30054 Human_SNP_ID_512769079 A-to-I Human chr12 + 98549264 98549264 98549264 TATTTTTTATGAGATGGAGTCTCACTCTTGTCACCCAGACTGTAGTGCAGTGGCACGATCTGGGC TATTTTTTATGAGATGGAGTCTCACTCTTGTCGCCCAGACTGTAGTGCAGTGGCACGATCTGGGC A G TMPO Ensembl:ENSG00000120802 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1371125751 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12068733,Human_RBP_ID_17561240,Human_RBP_ID_17829951,Human_RBP_ID_23306343,Human_RBP_ID_26420853 30055 RMVar_ID_30055 Human_SNP_ID_512769095 A-to-I Human chr12 + 98549304 98549304 98549304 TGTAGTGCAGTGGCACGATCTGGGCTCGATGCAACCTCTGCCTCCCAGGTTCAAGCAATTTTCCT TGTAGTGCAGTGGCACGATCTGGGCTCGATGCGACCTCTGCCTCCCAGGTTCAAGCAATTTTCCT A G TMPO Ensembl:ENSG00000120802 Protein coding 3'UTR GSE38233;GSE100210;GSE100210;GSE107867;GSE107867 cultured B-cells;HepG2 cell line;HepG2 cell line;ASD brains,cerebellum;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 24183664,29129909,29129909,30559470,30559470 RNA-Seq:(High) rs532861926 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_115757,Human_RBP_ID_6238679,Human_RBP_ID_17561240 30056 RMVar_ID_30056 Human_SNP_ID_512769100 A-to-I Human chr12 + 98549318 98549318 98549318 ACGATCTGGGCTCGATGCAACCTCTGCCTCCCAGGTTCAAGCAATTTTCCTGCCTCGGCAGAGAC ACGATCTGGGCTCGATGCAACCTCTGCCTCCCGGGTTCAAGCAATTTTCCTGCCTCGGCAGAGAC A G TMPO Ensembl:ENSG00000120802 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1174498646 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6238679,Human_RBP_ID_17561240 30057 RMVar_ID_30057 Human_SNP_ID_512769115 A-to-I Human chr12 + 98549359 98549359 98549359 CAATTTTCCTGCCTCGGCAGAGACGGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACCCCTGA CAATTTTCCTGCCTCGGCAGAGACGGGGTTTCCCCATGTTGGCCAGGCTGGTCTCGAACCCCTGA A C TMPO Ensembl:ENSG00000120802 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934398077 Functional Loss SNV dbSNP153 33..33 33 - - - 30058 RMVar_ID_30058 Human_SNP_ID_512769116 A-to-I Human chr12 + 98549359 98549359 98549359 CAATTTTCCTGCCTCGGCAGAGACGGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACCCCTGA CAATTTTCCTGCCTCGGCAGAGACGGGGTTTCGCCATGTTGGCCAGGCTGGTCTCGAACCCCTGA A G TMPO Ensembl:ENSG00000120802 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934398077 Functional Loss SNV dbSNP153 33..33 33 - - - 30059 RMVar_ID_30059 Human_SNP_ID_512769128 A-to-I Human chr12 + 98549409 98549409 98549409 GTCTCGAACCCCTGACCTCAAGTGATCAGCCCACCTCAGCTTCCCAAAGTGCTGGGATTACAGGT GTCTCGAACCCCTGACCTCAAGTGATCAGCCCGCCTCAGCTTCCCAAAGTGCTGGGATTACAGGT A G TMPO Ensembl:ENSG00000120802 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs3177178 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23159478,Human_RBP_ID_25014610,Human_RBP_ID_26421547 Human_miRNA_ID_1701898 30060 RMVar_ID_30060 Human_SNP_ID_512769133 A-to-I Human chr12 + 98549414 98549414 98549414 GAACCCCTGACCTCAAGTGATCAGCCCACCTCAGCTTCCCAAAGTGCTGGGATTACAGGTGTGAT GAACCCCTGACCTCAAGTGATCAGCCCACCTCTGCTTCCCAAAGTGCTGGGATTACAGGTGTGAT A T TMPO Ensembl:ENSG00000120802 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs138693048 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23159478,Human_RBP_ID_25014610,Human_RBP_ID_26421547 30061 RMVar_ID_30061 Human_SNP_ID_512769134 A-to-I Human chr12 + 98549423 98549423 98549423 ACCTCAAGTGATCAGCCCACCTCAGCTTCCCAAAGTGCTGGGATTACAGGTGTGATCCACTGCAC ACCTCAAGTGATCAGCCCACCTCAGCTTCCCAGAGTGCTGGGATTACAGGTGTGATCCACTGCAC A G TMPO Ensembl:ENSG00000120802 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-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 30062 RMVar_ID_30062 Human_SNP_ID_512769138 A-to-I Human chr12 + 98549438 98549438 98549438 CCCACCTCAGCTTCCCAAAGTGCTGGGATTACAGGTGTGATCCACTGCACCCGGCCGGCATTATG CCCACCTCAGCTTCCCAAAGTGCTGGGATTACGGGTGTGATCCACTGCACCCGGCCGGCATTATG A G TMPO Ensembl:ENSG00000120802 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1240883050 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229895,Human_RBP_ID_431043,Human_RBP_ID_23159478,Human_RBP_ID_26421547 Human_miRNA_ID_1143786 30063 RMVar_ID_30063 Human_SNP_ID_512770090 A-to-I Human chr12 + 98552864 98552864 98552864 AGAATCGCTTGGACCCGAGAGGTGGAGGTTTTAGTGAGCCGAGATCTTGCCATTGCACTCCAGCC AGAATCGCTTGGACCCGAGAGGTGGAGGTTTTGGTGAGCCGAGATCTTGCCATTGCACTCCAGCC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1302995795 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17829978 30064 RMVar_ID_30064 Human_SNP_ID_512781474 A-to-I Human chr12 + 98596830 98596830 98596830 GAGGTCAGGAGTTCGAGATCAGAACTCAATCTAGCCAACATGGTGAAACCTCATCTCTGCTAAAA GAGGTCAGGAGTTCGAGATCAGAACTCAATCTGGCCAACATGGTGAAACCTCATCTCTGCTAAAA A G SLC25A3 Ensembl:ENSG00000075415 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1291263606 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 30065 RMVar_ID_30065 Human_SNP_ID_512781478 A-to-I Human chr12 + 98596844 98596844 98596844 GAGATCAGAACTCAATCTAGCCAACATGGTGAAACCTCATCTCTGCTAAAAATACAAAAATTAGC GAGATCAGAACTCAATCTAGCCAACATGGTGACACCTCATCTCTGCTAAAAATACAAAAATTAGC A C SLC25A3 Ensembl:ENSG00000075415 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1289599729 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 30066 RMVar_ID_30066 Human_SNP_ID_512781483 A-to-I Human chr12 + 98596865 98596865 98596865 CAACATGGTGAAACCTCATCTCTGCTAAAAATACAAAAATTAGCTGGGCATGGTGGCGTGCCTGT CAACATGGTGAAACCTCATCTCTGCTAAAAATGCAAAAATTAGCTGGGCATGGTGGCGTGCCTGT A G SLC25A3 Ensembl:ENSG00000075415 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1417744132 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 30067 RMVar_ID_30067 Human_SNP_ID_512781489 A-to-I Human chr12 + 98596874 98596874 98596874 GAAACCTCATCTCTGCTAAAAATACAAAAATTAGCTGGGCATGGTGGCGTGCCTGTAGTCGCAGC GAAACCTCATCTCTGCTAAAAATACAAAAATTGGCTGGGCATGGTGGCGTGCCTGTAGTCGCAGC A G SLC25A3 Ensembl:ENSG00000075415 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-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 30068 RMVar_ID_30068 Human_SNP_ID_512781499 A-to-I Human chr12 + 98596898 98596898 98596898 CAAAAATTAGCTGGGCATGGTGGCGTGCCTGTAGTCGCAGCTACTCGGGAGGCTGAGGCAGGAGA CAAAAATTAGCTGGGCATGGTGGCGTGCCTGTGGTCGCAGCTACTCGGGAGGCTGAGGCAGGAGA A G SLC25A3 Ensembl:ENSG00000075415 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs895015130 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 30069 RMVar_ID_30069 Human_SNP_ID_512781655 A-to-I Human chr12 + 98597476 98597476 98597476 CTCTGCTGCCCAGGCTGGAGTGTAGTGGTGCCATCGTGGCTCACTGCAACCTCCACCTCCCTCCC CTCTGCTGCCCAGGCTGGAGTGTAGTGGTGCCGTCGTGGCTCACTGCAACCTCCACCTCCCTCCC A G SLC25A3 Ensembl:ENSG00000075415 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1216954853 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 30070 RMVar_ID_30070 Human_SNP_ID_512781683 A-to-I Human chr12 + 98597563 98597563 98597563 TCTCACCCTCACCCTCCCGAGTAGCTGGGATTACAGGTGCACGCCACCATGCCCGTCCAATTTTT TCTCACCCTCACCCTCCCGAGTAGCTGGGATTGCAGGTGCACGCCACCATGCCCGTCCAATTTTT A G SLC25A3 Ensembl:ENSG00000075415 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs968125958 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 30071 RMVar_ID_30071 Human_SNP_ID_512781695 A-to-I Human chr12 + 98597589 98597589 98597589 GGGATTACAGGTGCACGCCACCATGCCCGTCCAATTTTTTGTATTTTAGTAGAGATGGGGTTTCA GGGATTACAGGTGCACGCCACCATGCCCGTCCCATTTTTTGTATTTTAGTAGAGATGGGGTTTCA A C SLC25A3 Ensembl:ENSG00000075415 Protein coding intron GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-Seq:(High) rs1281384719 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 30072 RMVar_ID_30072 Human_SNP_ID_512781710 A-to-I Human chr12 + 98597662 98597662 98597662 CCCAGGCTGGTCTTGAACTCCTGAGCTCAGGTAATCCACCTGCCTCAGCCTCCCAAAGTGCTGGG CCCAGGCTGGTCTTGAACTCCTGAGCTCAGGTGATCCACCTGCCTCAGCCTCCCAAAGTGCTGGG A G SLC25A3 Ensembl:ENSG00000075415 Protein coding intron GSE47997;GSE126723:GSM3611827,GSM3611828,GSM3611829 K562 cells&HepG2 cells;Bronchiolar epithelium,BEP2D cell line - 23474544,31158229 RNA-Seq:(High) rs1387094590 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 30073 RMVar_ID_30073 Human_SNP_ID_512781715 A-to-I Human chr12 + 98597676 98597676 98597676 GAACTCCTGAGCTCAGGTAATCCACCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGATGTGAG GAACTCCTGAGCTCAGGTAATCCACCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGATGTGAG A G SLC25A3 Ensembl:ENSG00000075415 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs1163078159 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 30074 RMVar_ID_30074 Human_SNP_ID_512783762 A-to-I Human chr12 + 98604522 98604522 98604522 TTTTGACTTTTTTTTTTTTTTCCCTAGAGAACAGGGTTCTTGCTTTGTCGCCCAGGCTGGAGTAC TTTTGACTTTTTTTTTTTTTTCCCTAGAGAACGGGGTTCTTGCTTTGTCGCCCAGGCTGGAGTAC A G SLC25A3 Ensembl:ENSG00000075415 Protein coding 3'UTR GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;ASD brains,temporal_cortex;Bronchiolar epithelium,BEP2D cell line - 29129909,30559470,31158229 RNA-Seq:(High) rs1254322815 Functional Loss SNV dbSNP153 33..33 33 - - - 30075 RMVar_ID_30075 Human_SNP_ID_512783850 A-to-I Human chr12 + 98604831 98604831 98604831 GTCGCCAGACTGGAGTGCAGTGGCACGATGATAGCTCACTGCAGCCTCGATCTCCCAAGCTCAAG GTCGCCAGACTGGAGTGCAGTGGCACGATGATGGCTCACTGCAGCCTCGATCTCCCAAGCTCAAG A G SLC25A3 Ensembl:ENSG00000075415 Protein coding 3'UTR GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829 ASD brains,Fragile X samples from UC Davis FXTAS brain repository;Bronchiolar epithelium,BEP2D cell line - 30559470,31158229 RNA-Seq:(High) rs1439463077 Functional Loss SNV dbSNP153 33..33 33 - - - 30076 RMVar_ID_30076 Human_SNP_ID_512783947 A-to-I Human chr12 + 98605298 98605298 98605298 GGGTGTGGTGACACATGCCTGTAGTCTCAACTATTTGGGAGGCTGAGGCAGGAGGATTGCTTGAG GGGTGTGGTGACACATGCCTGTAGTCTCAACTCTTTGGGAGGCTGAGGCAGGAGGATTGCTTGAG A C SLC25A3 Ensembl:ENSG00000075415 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917086370 Functional Loss SNV dbSNP153 33..33 33 - - - 30077 RMVar_ID_30077 Human_SNP_ID_512783948 A-to-I Human chr12 + 98605298 98605298 98605298 GGGTGTGGTGACACATGCCTGTAGTCTCAACTATTTGGGAGGCTGAGGCAGGAGGATTGCTTGAG GGGTGTGGTGACACATGCCTGTAGTCTCAACTTTTTGGGAGGCTGAGGCAGGAGGATTGCTTGAG A T SLC25A3 Ensembl:ENSG00000075415 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917086370 Functional Loss SNV dbSNP153 33..33 33 - - - 30078 RMVar_ID_30078 Human_SNP_ID_512784084 A-to-I Human chr12 + 98605857 98605857 98605857 AATTGTATATCAGGCTGGGCACAGTGGCTCATACCCGTAATCCCAGCACTTTGGGAGGCCCAGGC AATTGTATATCAGGCTGGGCACAGTGGCTCATGCCCGTAATCCCAGCACTTTGGGAGGCCCAGGC A G SLC25A3 Ensembl:ENSG00000075415 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1428681764 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12069196 30079 RMVar_ID_30079 Human_SNP_ID_512784131 A-to-I Human chr12 + 98606037 98606037 98606037 CTTAGGAAGCTGAAGGAGGATCGTCTGAGCCCAGGAGTTTGAGGCTGCAATGAGCTACAATCACA CTTAGGAAGCTGAAGGAGGATCGTCTGAGCCCGGGAGTTTGAGGCTGCAATGAGCTACAATCACA A G SLC25A3 Ensembl:ENSG00000075415 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1133656 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12069197 30080 RMVar_ID_30080 Human_SNP_ID_512788003 A-to-I Human chr12 - 98620443 98620443 98620443 AGAATCTCTTGAAACCAGGAGGCAGGGGTTGCAGTGAGCTGAGATGGCGCCACTACACTCCAGCC AGAATCTCTTGAAACCAGGAGGCAGGGGTTGCGGTGAGCTGAGATGGCGCCACTACACTCCAGCC T C IKBIP Ensembl:ENSG00000166130 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956786036 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_159025 30081 RMVar_ID_30081 Human_SNP_ID_512788335 A-to-I Human chr12 - 98621815 98621815 98621815 CCTCAGCCTCCCAAAGTGCTGGGATTACAGACATGAGCCACCGCGTCCAGCCTTCATTATCGTCA CCTCAGCCTCCCAAAGTGCTGGGATTACAGACGTGAGCCACCGCGTCCAGCCTTCATTATCGTCA T C IKBIP Ensembl:ENSG00000166130 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1337356861 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_159025 30082 RMVar_ID_30082 Human_SNP_ID_512791360 A-to-I Human chr12 - 98632762 98632761 98632762 ATATTAGCTGAGCATGGTGGTTCATGCCTGTAATCCCAGCTACTTGGGAGGCTGATGTATGAGAA ATATTAGCTGAGCATGGTGGTTCATGCCTGTA_TCCCAGCTACTTGGGAGGCTGATGTATGAGAA AT A IKBIP Ensembl:ENSG00000166130 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs923698618 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_90534,RMVar_hsa_circ_159025,RMVar_hsa_circ_159026 30083 RMVar_ID_30083 Human_SNP_ID_512793277 A-to-I Human chr12 - 98640900 98640900 98640900 AAAATTAGCCAGGCATGGTGGCGCATGCCTGTAGTCCCAGCTACTTGGGGGGTTGAGGTTGGAGG AAAATTAGCCAGGCATGGTGGCGCATGCCTGTGGTCCCAGCTACTTGGGGGGTTGAGGTTGGAGG T C IKBIP Ensembl:ENSG00000166130 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025088347 Functional Loss SNV dbSNP153 33..33 33 - - - 30084 RMVar_ID_30084 Human_SNP_ID_512793290 A-to-I Human chr12 - 98640958 98640958 98640958 AGGAGTTCAAGACCAGCCTGGGCAACATGGTAAAACCCTGTCTCTACAAAAAATACAAAAAATTA AGGAGTTCAAGACCAGCCTGGGCAACATGGTAGAACCCTGTCTCTACAAAAAATACAAAAAATTA T C IKBIP Ensembl:ENSG00000166130 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350757738 Functional Loss SNV dbSNP153 33..33 33 - - - 30085 RMVar_ID_30085 Human_SNP_ID_512796145 A-to-I Human chr12 + 98651759 98651759 98651759 ATAGCTCACTGCAGCCTCAAACTTTTAGGCTCAAGTGATCCTCCCACCTTAGCCTCCTGAGGAGC ATAGCTCACTGCAGCCTCAAACTTTTAGGCTCGAGTGATCCTCCCACCTTAGCCTCCTGAGGAGC A G APAF1 Ensembl:ENSG00000120868 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs779196602 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7132,RMVar_hsa_circ_87394,RMVar_hsa_circ_105730,RMVar_hsa_circ_367424,RMVar_hsa_circ_159027,RMVar_hsa_circ_342683,RMVar_hsa_circ_315227,RMVar_hsa_circ_159029,RMVar_hsa_circ_52243,RMVar_hsa_circ_159028,RMVar_hsa_circ_47160,RMVar_hsa_circ_314555,RMVar_hsa_circ_336400,RMVar_hsa_circ_348978,RMVar_hsa_circ_50415,RMVar_hsa_circ_39878,RMVar_hsa_circ_159031,RMVar_hsa_circ_159032 30086 RMVar_ID_30086 Human_SNP_ID_512815650 A-to-I Human chr12 + 98733572 98733572 98733572 CTCCTGCCTCAGCCTCCCAAGTAGCTGAGACTACAGGCACGAGCCACCACACCCAGCTAATTTTT CTCCTGCCTCAGCCTCCCAAGTAGCTGAGACTGCAGGCACGAGCCACCACACCCAGCTAATTTTT A G APAF1 Ensembl:ENSG00000120868 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1131019 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105730,RMVar_hsa_circ_159027 30087 RMVar_ID_30087 Human_SNP_ID_512815661 A-to-I Human chr12 + 98733634 98733634 98733634 TTTAAGTTTTCTTGTAGAGACAGGGTCTCACTATGTTGTCTAGGCTGGTCTTGAACTCTTGGCCT TTTAAGTTTTCTTGTAGAGACAGGGTCTCACTGTGTTGTCTAGGCTGGTCTTGAACTCTTGGCCT A G APAF1 Ensembl:ENSG00000120868 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1470964302 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4245847 RMVar_hsa_circ_105730,RMVar_hsa_circ_159027 30088 RMVar_ID_30088 Human_SNP_ID_512815672 A-to-I Human chr12 + 98733686 98733686 98733686 GAACTCTTGGCCTCAAGTAATCCTCCTGCCTCAGCCTCCCAAAGTGTTGGGATTGCAGATATGAG GAACTCTTGGCCTCAAGTAATCCTCCTGCCTCGGCCTCCCAAAGTGTTGGGATTGCAGATATGAG A G APAF1 Ensembl:ENSG00000120868 Protein coding 3'UTR GSE123020:GSM3490829,GSM3490830,GSM3490831 esophageal squamous carcinoma cells,EC109 cell line - 32596459 RNA-Seq:(High) rs1387817272 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12069873 RMVar_hsa_circ_105730,RMVar_hsa_circ_159027 30089 RMVar_ID_30089 Human_SNP_ID_512815673 A-to-I Human chr12 + 98733695 98733695 98733695 GCCTCAAGTAATCCTCCTGCCTCAGCCTCCCAAAGTGTTGGGATTGCAGATATGAGCCACTGGCC GCCTCAAGTAATCCTCCTGCCTCAGCCTCCCAGAGTGTTGGGATTGCAGATATGAGCCACTGGCC A G APAF1 Ensembl:ENSG00000120868 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,31158229,32596459 RNA-Seq:(High) rs865866330 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12069873 RMVar_hsa_circ_105730,RMVar_hsa_circ_159027 30090 RMVar_ID_30090 Human_SNP_ID_512815914 A-to-I Human chr12 + 98735014 98735014 98735014 ACGTGCCTGTAATCCCAGCTCCTTGGGAGGCTAAGACAGGAGGATTCCTTGAGCCCTGGAGTTTG ACGTGCCTGTAATCCCAGCTCCTTGGGAGGCTGAGACAGGAGGATTCCTTGAGCCCTGGAGTTTG A G APAF1 Ensembl:ENSG00000120868 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1131021 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105730,RMVar_hsa_circ_159027 30091 RMVar_ID_30091 Human_SNP_ID_512822074 A-to-I Human chr12 - 98760441 98760441 98760441 GGCAACATGTTGAAACCCTGTCTCTAAAAAACATACAAAAATCAGCCAGGTGTGATGACACATTA GGCAACATGTTGAAACCCTGTCTCTAAAAAACCTACAAAAATCAGCCAGGTGTGATGACACATTA T G ANKS1B Ensembl:ENSG00000185046 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs777566967 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_159054,RMVar_hsa_circ_159052,RMVar_hsa_circ_110920,RMVar_hsa_circ_159051,RMVar_hsa_circ_265183,RMVar_hsa_circ_268518,RMVar_hsa_circ_296498,RMVar_hsa_circ_299316,RMVar_hsa_circ_283565,RMVar_hsa_circ_267840,RMVar_hsa_circ_159056,RMVar_hsa_circ_72436,RMVar_hsa_circ_159055,RMVar_hsa_circ_159053 30092 RMVar_ID_30092 Human_SNP_ID_512829094 A-to-I Human chr12 - 98791678 98791678 98791678 TAACATGCACTTGTACTCCCAGCTACTTGGGAAGCTGAGTCAGGAGGATCACTTCAACCCAGGAA TAACATGCACTTGTACTCCCAGCTACTTGGGAGGCTGAGTCAGGAGGATCACTTCAACCCAGGAA T C ANKS1B Ensembl:ENSG00000185046 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1352703009 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21880,RMVar_hsa_circ_159054,RMVar_hsa_circ_159052,RMVar_hsa_circ_110920,RMVar_hsa_circ_159051,RMVar_hsa_circ_265183,RMVar_hsa_circ_268518,RMVar_hsa_circ_296498,RMVar_hsa_circ_299316,RMVar_hsa_circ_283565,RMVar_hsa_circ_159056,RMVar_hsa_circ_159055,RMVar_hsa_circ_267422,RMVar_hsa_circ_159053,RMVar_hsa_circ_278377,RMVar_hsa_circ_309908,RMVar_hsa_circ_334562,RMVar_hsa_circ_281802,RMVar_hsa_circ_35156,RMVar_hsa_circ_29717,RMVar_hsa_circ_25880,RMVar_hsa_circ_159059,RMVar_hsa_circ_159061,RMVar_hsa_circ_159062,RMVar_hsa_circ_159060,RMVar_hsa_circ_333916,RMVar_hsa_circ_159058,RMVar_hsa_circ_293711,RMVar_hsa_circ_159067,RMVar_hsa_circ_159063,RMVar_hsa_circ_159065,RMVar_hsa_circ_159066,RMVar_hsa_circ_159064,RMVar_hsa_circ_88182 30093 RMVar_ID_30093 Human_SNP_ID_512829772 A-to-I Human chr12 - 98794615 98794615 98794615 TGCTTTGGTCCACCTAACTTTGTGAGGATCGCACTTCTTTTTAAAGTTTTTAATGACATTTAGAT TGCTTTGGTCCACCTAACTTTGTGAGGATCGCTCTTCTTTTTAAAGTTTTTAATGACATTTAGAT T A ANKS1B Ensembl:ENSG00000185046 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs776548641 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21880,RMVar_hsa_circ_159054,RMVar_hsa_circ_159052,RMVar_hsa_circ_110920,RMVar_hsa_circ_159051,RMVar_hsa_circ_265183,RMVar_hsa_circ_268518,RMVar_hsa_circ_296498,RMVar_hsa_circ_299316,RMVar_hsa_circ_283565,RMVar_hsa_circ_159056,RMVar_hsa_circ_159055,RMVar_hsa_circ_267422,RMVar_hsa_circ_159053,RMVar_hsa_circ_278377,RMVar_hsa_circ_309908,RMVar_hsa_circ_334562,RMVar_hsa_circ_281802,RMVar_hsa_circ_35156,RMVar_hsa_circ_29717,RMVar_hsa_circ_25880,RMVar_hsa_circ_159059,RMVar_hsa_circ_159061,RMVar_hsa_circ_159062,RMVar_hsa_circ_159060,RMVar_hsa_circ_333916,RMVar_hsa_circ_159058,RMVar_hsa_circ_293711,RMVar_hsa_circ_159067,RMVar_hsa_circ_159063,RMVar_hsa_circ_159065,RMVar_hsa_circ_159066,RMVar_hsa_circ_159064,RMVar_hsa_circ_88182 30094 RMVar_ID_30094 Human_SNP_ID_512860602 A-to-I Human chr12 - 98929653 98929622 98929654 GATTACCTTGGCACTCTTACTGAAAATCAGTTAACCCTGTAAAAGCCTGCTACTGAACTACTGAA GATTACCTTGGCACTCTTACTGAAAATCAGT________________________________AA TCAGTAGTTCAGTAGCAGGCTTTTACAGGGTTA T ANKS1B Ensembl:ENSG00000185046 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs569913445 Functional Loss DEL dbSNP153 32..63 33 - - - RMVar_hsa_circ_8014,RMVar_hsa_circ_110920,RMVar_hsa_circ_159051,RMVar_hsa_circ_35156,RMVar_hsa_circ_29717,RMVar_hsa_circ_29948,RMVar_hsa_circ_159067,RMVar_hsa_circ_88182,RMVar_hsa_circ_40956,RMVar_hsa_circ_20541 30095 RMVar_ID_30095 Human_SNP_ID_512861438 A-to-I Human chr12 - 98933665 98933664 98933665 CACCTGTCTGGATGAGTATTATTTTTTTAAAAAGACACCAAATGTCAAGAATGTGGAGAAATTGA CACCTGTCTGGATGAGTATTATTTTTTTAAAA_GACACCAAATGTCAAGAATGTGGAGAAATTGA CT C ANKS1B Ensembl:ENSG00000185046 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1342077622 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_8014,RMVar_hsa_circ_110920,RMVar_hsa_circ_159051,RMVar_hsa_circ_35156,RMVar_hsa_circ_29717,RMVar_hsa_circ_29948,RMVar_hsa_circ_159067,RMVar_hsa_circ_88182,RMVar_hsa_circ_40956,RMVar_hsa_circ_20541 30096 RMVar_ID_30096 Human_SNP_ID_512861822 A-to-I Human chr12 - 98935505 98935505 98935505 AAACTCTTCCAAAAACTTGAAGAGGGAAGAATACTTCCAAATTTATTTTATGAGACCAGCATTAT AAACTCTTCCAAAAACTTGAAGAGGGAAGAATCCTTCCAAATTTATTTTATGAGACCAGCATTAT T G ANKS1B Ensembl:ENSG00000185046 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs568020496 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8014,RMVar_hsa_circ_110920,RMVar_hsa_circ_159051,RMVar_hsa_circ_35156,RMVar_hsa_circ_29717,RMVar_hsa_circ_29948,RMVar_hsa_circ_159067,RMVar_hsa_circ_88182,RMVar_hsa_circ_40956,RMVar_hsa_circ_20541 30097 RMVar_ID_30097 Human_SNP_ID_512868306 A-to-I Human chr12 - 98963424 98963424 98963424 CCTGTAATCCCAGCACTTTGGGAGGCCATAGCAGGTGGCTCACTTGAGACCAGGAGTTTGGGACC CCTGTAATCCCAGCACTTTGGGAGGCCATAGCGGGTGGCTCACTTGAGACCAGGAGTTTGGGACC T C ANKS1B Ensembl:ENSG00000185046 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1215071020 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8014,RMVar_hsa_circ_110920,RMVar_hsa_circ_159051,RMVar_hsa_circ_35156,RMVar_hsa_circ_29717,RMVar_hsa_circ_29948,RMVar_hsa_circ_159067,RMVar_hsa_circ_88182,RMVar_hsa_circ_40956,RMVar_hsa_circ_20541 30098 RMVar_ID_30098 Human_SNP_ID_512907886 A-to-I Human chr12 - 99139235 99139235 99139235 GAAAGAGAGGAAGAAGAAAGAAAGAGAGAAGGAAGGAAGGAAAGAAAGAGAAGGAAGGAAGGAAA GAAAGAGAGGAAGAAGAAAGAAAGAGAGAAGGCAGGAAGGAAAGAAAGAGAAGGAAGGAAGGAAA T G ANKS1B Ensembl:ENSG00000185046 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs568934738 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8014,RMVar_hsa_circ_110920,RMVar_hsa_circ_159051,RMVar_hsa_circ_29717,RMVar_hsa_circ_29948,RMVar_hsa_circ_159067,RMVar_hsa_circ_88182,RMVar_hsa_circ_40956,RMVar_hsa_circ_20541,RMVar_hsa_circ_314122,RMVar_hsa_circ_331269,RMVar_hsa_circ_344018,RMVar_hsa_circ_314379,RMVar_hsa_circ_308530,RMVar_hsa_circ_17020,RMVar_hsa_circ_57682,RMVar_hsa_circ_38436,RMVar_hsa_circ_66928,RMVar_hsa_circ_363409,RMVar_hsa_circ_354015,RMVar_hsa_circ_39710 30099 RMVar_ID_30099 Human_SNP_ID_512966196 A-to-I Human chr12 - 99385306 99385306 99385306 TGCCAGCACGCCCAGCTGATTTTTGTATTTTTAGTAGAGATGGGGTTTTGCCATGTTGGCCAGGC TGCCAGCACGCCCAGCTGATTTTTGTATTTTTGGTAGAGATGGGGTTTTGCCATGTTGGCCAGGC T C ANKS1B Ensembl:ENSG00000185046 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs911427842 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110920,RMVar_hsa_circ_159051,RMVar_hsa_circ_159067,RMVar_hsa_circ_88182,RMVar_hsa_circ_314122,RMVar_hsa_circ_331269,RMVar_hsa_circ_344018,RMVar_hsa_circ_17020,RMVar_hsa_circ_57682,RMVar_hsa_circ_38436,RMVar_hsa_circ_66928,RMVar_hsa_circ_354015,RMVar_hsa_circ_20877,RMVar_hsa_circ_71119,RMVar_hsa_circ_304145,RMVar_hsa_circ_345759,RMVar_hsa_circ_372355,RMVar_hsa_circ_18745,RMVar_hsa_circ_31009,RMVar_hsa_circ_159081,RMVar_hsa_circ_159083,RMVar_hsa_circ_159084 30100 RMVar_ID_30100 Human_SNP_ID_446603242 A-to-I Human chr10 - 109528610 109528610 109528610 CTGAAGTCCTTGGCCCTCTCTGGCAGCTCCCAATGAATCAACAGGGATACCTGGGCCCACTGGGT CTGAAGTCCTTGGCCCTCTCTGGCAGCTCCCAGTGAATCAACAGGGATACCTGGGCCCACTGGGT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1004984464 Functional Loss SNV dbSNP153 33..33 33 - - - 30101 RMVar_ID_30101 Human_SNP_ID_446704298 A-to-I Human chr10 - 109907743 109907743 109907743 GCAGCTGAGACAAGCCATGAGGAACTCTGAGTATGTGACCGAACCGATCCAGGCCTACATCATCC GCAGCTGAGACAAGCCATGAGGAACTCTGAGTGTGTGACCGAACCGATCCAGGCCTACATCATCC T C XPNPEP1 Ensembl:ENSG00000108039 Protein coding exon GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs987799582 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18971272,Human_RBP_ID_23432857 Human_Splice_Rec_1174720,Human_Splice_Rec_1174721,Human_Splice_Rec_1174752,Human_Splice_Rec_1174753,Human_Splice_Rec_1174790,Human_Splice_Rec_1174791,Human_Splice_Rec_1174830,Human_Splice_Rec_1174831,Human_Splice_Rec_1174954,Human_Splice_Rec_1174955,Human_Splice_Rec_1174966,Human_Splice_Rec_1174967,Human_Splice_Rec_1174984,Human_Splice_Rec_1174985,Human_Splice_Rec_1174997,Human_Splice_Rec_1175038,Human_Splice_Rec_1175039,Human_Splice_Rec_1175064,Human_Splice_Rec_1175065,Human_Splice_Rec_1175080,Human_Splice_Rec_1175081,Human_Splice_Rec_1175098,Human_Splice_Rec_1175099,Human_Splice_Rec_1175105 RMVar_hsa_circ_146329,RMVar_hsa_circ_328100,RMVar_hsa_circ_333206,RMVar_hsa_circ_298794,RMVar_hsa_circ_330506 30102 RMVar_ID_30102 Human_SNP_ID_446875874 A-to-I Human chr10 + 110588015 110588014 110588016 AGTCATTCTGATTATCCAAGATTTTTTGAGACAGAGTCTCGCTGTGTCACCAGGTTGGAGTGCAG AGTCATTCTGATTATCCAAGATTTTTTGAGAC__AGTCTCGCTGTGTCACCAGGTTGGAGTGCAG CAG C SMC3 Ensembl:ENSG00000108055 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1261340191 Functional Loss DEL dbSNP153 33..34 33 - - - 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_146362,RMVar_hsa_circ_146364,RMVar_hsa_circ_146365,RMVar_hsa_circ_64678,RMVar_hsa_circ_146367,RMVar_hsa_circ_98345,RMVar_hsa_circ_57741 30103 RMVar_ID_30103 Human_SNP_ID_446948208 A-to-I Human chr10 + 110881493 110881493 110881493 TGCCAACCAGTCCAAAGGGAAGGTTGCTGGATAGGCGATCCAGATCTGGGAAAGGAAGGGGACTA TGCCAACCAGTCCAAAGGGAAGGTTGCTGGATGGGCGATCCAGATCTGGGAAAGGAAGGGGACTA A G PDCD4 Ensembl:ENSG00000150593 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs775450189 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5925426,Human_RBP_ID_9360785,Human_RBP_ID_17769338,Human_RBP_ID_23433745 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 30104 RMVar_ID_30104 Human_SNP_ID_446954565 A-to-I Human chr10 - 110906824 110906824 110906824 TGGGCACAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAACGGGGGCGGATCACTTGA TGGGCACAGTGGCTCACGCCTGTAATCCCAGCGCTTTGGGAGGCCAACGGGGGCGGATCACTTGA T C BBIP1 Ensembl:ENSG00000214413 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1425554115 Functional Loss SNV dbSNP153 33..33 33 - - - 30105 RMVar_ID_30105 Human_SNP_ID_446954682 A-to-I Human chr10 - 110907271 110907271 110907271 GGCTCAAGCGATCCTCCCACTTTGGCCTTCCAAAGTGCTGGGATTCCAGATGCGAGCCACCGCAC GGCTCAAGCGATCCTCCCACTTTGGCCTTCCAGAGTGCTGGGATTCCAGATGCGAGCCACCGCAC T C BBIP1 Ensembl:ENSG00000214413 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1297228370 Functional Loss SNV dbSNP153 33..33 33 - - - 30106 RMVar_ID_30106 Human_SNP_ID_446954691 A-to-I Human chr10 - 110907320 110907320 110907320 TTTTGTAGAGATGAGGTCTTGCTTTGTTGTCTAGGCTGGTCTTGAACTGGGCTCAAGCGATCCTC TTTTGTAGAGATGAGGTCTTGCTTTGTTGTCTGGGCTGGTCTTGAACTGGGCTCAAGCGATCCTC T C BBIP1 Ensembl:ENSG00000214413 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1199486159 Functional Loss SNV dbSNP153 33..33 33 - - - 30107 RMVar_ID_30107 Human_SNP_ID_446954730 A-to-I Human chr10 - 110907482 110907482 110907482 TTGAGACAAGCTCTTACTCTGTCACCTAAGCTAGAATGCAGTGGCGTGATCATATCTCACTGCAA TTGAGACAAGCTCTTACTCTGTCACCTAAGCTGGAATGCAGTGGCGTGATCATATCTCACTGCAA T C BBIP1 Ensembl:ENSG00000214413 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1305428239 Functional Loss SNV dbSNP153 33..33 33 - - - 30108 RMVar_ID_30108 Human_SNP_ID_446962132 A-to-I Human chr10 + 110937034 110937034 110937034 GGCTGGGGGCCCGGAAGTGGTAGGGGCGTCGGAAAGGGTTGGTGTTCATCCGCTTGCGGAGGAAA GGCTGGGGGCCCGGAAGTGGTAGGGGCGTCGGGAAGGGTTGGTGTTCATCCGCTTGCGGAGGAAA A G SHOC2 Ensembl:ENSG00000108061 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs746309763 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5925850,Human_RBP_ID_24780950 RMVar_hsa_circ_146386,RMVar_hsa_circ_90319 30109 RMVar_ID_30109 Human_SNP_ID_446962133 A-to-I Human chr10 + 110937034 110937034 110937034 GGCTGGGGGCCCGGAAGTGGTAGGGGCGTCGGAAAGGGTTGGTGTTCATCCGCTTGCGGAGGAAA GGCTGGGGGCCCGGAAGTGGTAGGGGCGTCGGTAAGGGTTGGTGTTCATCCGCTTGCGGAGGAAA A T SHOC2 Ensembl:ENSG00000108061 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs746309763 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5925850,Human_RBP_ID_24780950 RMVar_hsa_circ_146386,RMVar_hsa_circ_90319 30110 RMVar_ID_30110 Human_SNP_ID_447274603 A-to-I Human chr10 - 112134108 112134108 112134108 TATGGTCTGAGGTGGGCAGGTCAAATGAAACTACATGCGATGTGTGTATTTTATTTGGATCCTGA TATGGTCTGAGGTGGGCAGGTCAAATGAAACTTCATGCGATGTGTGTATTTTATTTGGATCCTGA T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs890783835 Functional Loss SNV dbSNP153 33..33 33 - - - 30111 RMVar_ID_30111 Human_SNP_ID_447274604 A-to-I Human chr10 - 112134108 112134108 112134108 TATGGTCTGAGGTGGGCAGGTCAAATGAAACTACATGCGATGTGTGTATTTTATTTGGATCCTGA TATGGTCTGAGGTGGGCAGGTCAAATGAAACTGCATGCGATGTGTGTATTTTATTTGGATCCTGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs890783835 Functional Loss SNV dbSNP153 33..33 33 - - - 30112 RMVar_ID_30112 Human_SNP_ID_447274608 A-to-I Human chr10 - 112134117 112134117 112134117 TGAAGGTCCTATGGTCTGAGGTGGGCAGGTCAAATGAAACTACATGCGATGTGTGTATTTTATTT TGAAGGTCCTATGGTCTGAGGTGGGCAGGTCAGATGAAACTACATGCGATGTGTGTATTTTATTT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1319806065 Functional Loss SNV dbSNP153 33..33 33 - - - 30113 RMVar_ID_30113 Human_SNP_ID_447341159 A-to-I Human chr10 + 112405370 112405370 112405370 TTCAAACGCTCCCTAGAAATGCAGCATATGATACATATAACATACAAAATCTGTGTTAACTGTCT TTCAAACGCTCCCTAGAAATGCAGCATATGATGCATATAACATACAAAATCTGTGTTAACTGTCT A G ACSL5 Ensembl:ENSG00000197142 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1040411635 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17559207 RMVar_hsa_circ_66021,RMVar_hsa_circ_368907,RMVar_hsa_circ_58702,RMVar_hsa_circ_368906 30114 RMVar_ID_30114 Human_SNP_ID_447352178 A-to-I Human chr10 + 112449496 112449496 112449496 TAAAACTGGGCAGAGCCCGGTGGCTCATGCCTATAATCCCAAAACTTTGGGAGGCCGAGGCAGAC TAAAACTGGGCAGAGCCCGGTGGCTCATGCCTGTAATCCCAAAACTTTGGGAGGCCGAGGCAGAC A G VTI1A Ensembl:ENSG00000151532 Protein coding exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1316804467 Functional Loss SNV dbSNP153 33..33 33 - - - 30115 RMVar_ID_30115 Human_SNP_ID_447352194 A-to-I Human chr10 + 112449534 112449534 112449534 CCAAAACTTTGGGAGGCCGAGGCAGACGGATCACCTGAGGTCGGGAGTTTGAGACCAGCCTGGCC CCAAAACTTTGGGAGGCCGAGGCAGACGGATCGCCTGAGGTCGGGAGTTTGAGACCAGCCTGGCC A G VTI1A Ensembl:ENSG00000151532 Protein coding exon GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs943122556 Functional Loss SNV dbSNP153 33..33 33 - - - 30116 RMVar_ID_30116 Human_SNP_ID_447352195 A-to-I Human chr10 + 112449534 112449534 112449534 CCAAAACTTTGGGAGGCCGAGGCAGACGGATCACCTGAGGTCGGGAGTTTGAGACCAGCCTGGCC CCAAAACTTTGGGAGGCCGAGGCAGACGGATCTCCTGAGGTCGGGAGTTTGAGACCAGCCTGGCC A T VTI1A Ensembl:ENSG00000151532 Protein coding exon GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs943122556 Functional Loss SNV dbSNP153 33..33 33 - - - 30117 RMVar_ID_30117 Human_SNP_ID_447352212 A-to-I Human chr10 + 112449594 112449594 112449594 TGGCCAACATGGAGAAACCCTGTCTCTACTAAAAATACAAAACTAGCTGGGCGTGGTGGCACATG TGGCCAACATGGAGAAACCCTGTCTCTACTAAGAATACAAAACTAGCTGGGCGTGGTGGCACATG A G VTI1A Ensembl:ENSG00000151532 Protein coding exon GSE38233;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,32596459 RNA-Seq:(High) rs1212265400 Functional Loss SNV dbSNP153 33..33 33 - - - 30118 RMVar_ID_30118 Human_SNP_ID_447352225 A-to-I Human chr10 + 112449659 112449659 112449659 CCTGTAACTCCAGCTGCTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACCTGGGAGGTGGAGGTT CCTGTAACTCCAGCTGCTCAGGAGGCTGAGGCGGGAGAATCGCTTGAACCTGGGAGGTGGAGGTT A G VTI1A Ensembl:ENSG00000151532 Protein coding exon GSE38233;GSE99789;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29796672,32596459 RNA-Seq:(High) rs1419285386 Functional Loss SNV dbSNP153 33..33 33 - - - 30119 RMVar_ID_30119 Human_SNP_ID_447352327 A-to-I Human chr10 + 112450010 112449994 112450011 CAACCTCTCCCTCACGGCTCAAGTCTACTCCCACCTCAGCCTCCCGAGTAGCTGGGACTACTCAA CAACCTCTCCCTCACGG_________________CTCAGCCTCCCGAGTAGCTGGGACTACTCAA GCTCAAGTCTACTCCCAC G VTI1A Ensembl:ENSG00000151532 Protein coding exon GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs950900261 Functional Loss DEL dbSNP153 18..34 33 - - - Human_RBP_ID_370173 30120 RMVar_ID_30120 Human_SNP_ID_447352333 A-to-I Human chr10 + 112450010 112450010 112450010 CAACCTCTCCCTCACGGCTCAAGTCTACTCCCACCTCAGCCTCCCGAGTAGCTGGGACTACTCAA CAACCTCTCCCTCACGGCTCAAGTCTACTCCCCCCTCAGCCTCCCGAGTAGCTGGGACTACTCAA A C VTI1A Ensembl:ENSG00000151532 Protein coding exon GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs942388842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_370173 30121 RMVar_ID_30121 Human_SNP_ID_447412126 A-to-I Human chr10 + 112702847 112702847 112702847 GGCTCAATGGATCCACCCACCTTGGCCTCCCAAAGTGCTGGGATTATAGGTGTGACCCACTGCGC GGCTCAATGGATCCACCCACCTTGGCCTCCCAGAGTGCTGGGATTATAGGTGTGACCCACTGCGC A G VTI1A Ensembl:ENSG00000151532 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1014420416 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123376,RMVar_hsa_circ_146420 30122 RMVar_ID_30122 Human_SNP_ID_447480104 A-to-I Human chr10 + 112979731 112979731 112979731 TGAGCAGAGATGGCGCCACTGTACTCCAGCCTAGGTGACGGAGCAAGACCCTGTCTCAAAAAAAA TGAGCAGAGATGGCGCCACTGTACTCCAGCCTCGGTGACGGAGCAAGACCCTGTCTCAAAAAAAA A C TCF7L2 Ensembl:ENSG00000148737 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006175172 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_146428,RMVar_hsa_circ_288183,RMVar_hsa_circ_51712,RMVar_hsa_circ_283595 30123 RMVar_ID_30123 Human_SNP_ID_447480877 A-to-I Human chr10 + 112982825 112982825 112982825 TTTTGTATTTTTAGTAGAGACAGGGTTTTGCCATGTTGGCCTGGCTGCTCTTGAACTCCTGACCT TTTTGTATTTTTAGTAGAGACAGGGTTTTGCCTTGTTGGCCTGGCTGCTCTTGAACTCCTGACCT A T TCF7L2 Ensembl:ENSG00000148737 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs750265212 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11264515 RMVar_hsa_circ_146428,RMVar_hsa_circ_288183,RMVar_hsa_circ_51712,RMVar_hsa_circ_283595 30124 RMVar_ID_30124 Human_SNP_ID_447504405 A-to-I Human chr10 + 113076303 113076300 113076304 GGGACTATAGGTGTGAATTACCATGCCTGGCTAACTTTTTTATTTTTTGTAGAGACAGGGTCTTA GGGACTATAGGTGTGAATTACCATGCCTGG____CTTTTTTATTTTTTGTAGAGACAGGGTCTTA GCTAA G TCF7L2 Ensembl:ENSG00000148737 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1297431338 Functional Loss DEL dbSNP153 31..34 33 - - - RMVar_hsa_circ_283595,RMVar_hsa_circ_73025,RMVar_hsa_circ_366191,RMVar_hsa_circ_302329,RMVar_hsa_circ_146431 30125 RMVar_ID_30125 Human_SNP_ID_447504407 A-to-I Human chr10 + 113076312 113076306 113076312 GGTGTGAATTACCATGCCTGGCTAACTTTTTTATTTTTTGTAGAGACAGGGTCTTACCCTATTGC GGTGTGAATTACCATGCCTGGCTAACT______TTTTTTGTAGAGACAGGGTCTTACCCTATTGC TTTTTTA T TCF7L2 Ensembl:ENSG00000148737 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1313902131 Functional Loss DEL dbSNP153 28..33 33 - - - RMVar_hsa_circ_283595,RMVar_hsa_circ_73025,RMVar_hsa_circ_366191,RMVar_hsa_circ_302329,RMVar_hsa_circ_146431 30126 RMVar_ID_30126 Human_SNP_ID_447504408 A-to-I Human chr10 + 113076312 113076312 113076312 GGTGTGAATTACCATGCCTGGCTAACTTTTTTATTTTTTGTAGAGACAGGGTCTTACCCTATTGC GGTGTGAATTACCATGCCTGGCTAACTTTTTTCTTTTTTGTAGAGACAGGGTCTTACCCTATTGC A C TCF7L2 Ensembl:ENSG00000148737 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1338350622 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_283595,RMVar_hsa_circ_73025,RMVar_hsa_circ_366191,RMVar_hsa_circ_302329,RMVar_hsa_circ_146431 30127 RMVar_ID_30127 Human_SNP_ID_447504409 A-to-I Human chr10 + 113076312 113076312 113076312 GGTGTGAATTACCATGCCTGGCTAACTTTTTTATTTTTTGTAGAGACAGGGTCTTACCCTATTGC GGTGTGAATTACCATGCCTGGCTAACTTTTTTGTTTTTTGTAGAGACAGGGTCTTACCCTATTGC A G TCF7L2 Ensembl:ENSG00000148737 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1338350622 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_283595,RMVar_hsa_circ_73025,RMVar_hsa_circ_366191,RMVar_hsa_circ_302329,RMVar_hsa_circ_146431 30128 RMVar_ID_30128 Human_SNP_ID_447513008 A-to-I Human chr10 + 113109415 113109415 113109415 TTATTTGTTTATTTATTTTTTTGAGACAGGACAGGCTCTGGCTCTGTCGCCCAGGCTGGAGTGCA TTATTTGTTTATTTATTTTTTTGAGACAGGACGGGCTCTGGCTCTGTCGCCCAGGCTGGAGTGCA A G TCF7L2 Ensembl:ENSG00000148737 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1425736393 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5928799,Human_RBP_ID_11266145 RMVar_hsa_circ_6201,RMVar_hsa_circ_73025,RMVar_hsa_circ_366191 30129 RMVar_ID_30129 Human_SNP_ID_447513036 A-to-I Human chr10 + 113109520 113109520 113109520 TCAAGTAATTCTTTTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCTCCTGCCACCACGCCCA TCAAGTAATTCTTTTGCCTCAGCCTCCCAAGTGGCTGGGATTACAGGCTCCTGCCACCACGCCCA A G TCF7L2 Ensembl:ENSG00000148737 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs944634448 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6201,RMVar_hsa_circ_73025,RMVar_hsa_circ_366191 30130 RMVar_ID_30130 Human_SNP_ID_447525343 A-to-I Human chr10 + 113157223 113157223 113157223 TCACTGCAACCTCCGCCTTCTGGGTTCAGGCGATTCTCCTGCCTCGGCCTCCCGAGTAGCTGGGG TCACTGCAACCTCCGCCTTCTGGGTTCAGGCGTTTCTCCTGCCTCGGCCTCCCGAGTAGCTGGGG A T TCF7L2 Ensembl:ENSG00000148737 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1484162827 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73025,RMVar_hsa_circ_40438,RMVar_hsa_circ_59641 30131 RMVar_ID_30131 Human_SNP_ID_447701879 A-to-I Human chr10 + 113864442 113864442 113864442 CAAAAATGAGCCAGGCGTGGTGTCTCACGCCTATAATCCCAGCACTTTGGGAGGCCAAGGCAGGC CAAAAATGAGCCAGGCGTGGTGTCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGC A G NHLRC2 Ensembl:ENSG00000196865 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs952343780 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42738,RMVar_hsa_circ_45724,RMVar_hsa_circ_368005 30132 RMVar_ID_30132 Human_SNP_ID_447701929 A-to-I Human chr10 + 113864638 113864638 113864638 AGAATCGCTTGAACCCACGAGGCAGAGATTGCAGTGAGCTGAGATTGCGCCACTGAACTCTAGCC AGAATCGCTTGAACCCACGAGGCAGAGATTGCGGTGAGCTGAGATTGCGCCACTGAACTCTAGCC A G NHLRC2 Ensembl:ENSG00000196865 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1487322166 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42738,RMVar_hsa_circ_45724,RMVar_hsa_circ_368005 30133 RMVar_ID_30133 Human_SNP_ID_447703034 A-to-I Human chr10 + 113868960 113868960 113868960 CCAAAGGAAGTCCTAGAATATACTGCAGGAGGAAAAGAGTGTGGAGAAGATACTGGAGAGATGAG CCAAAGGAAGTCCTAGAATATACTGCAGGAGGGAAAGAGTGTGGAGAAGATACTGGAGAGATGAG A G NHLRC2 Ensembl:ENSG00000196865 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs542434821 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42738,RMVar_hsa_circ_45724,RMVar_hsa_circ_368005 30134 RMVar_ID_30134 Human_SNP_ID_447703035 A-to-I Human chr10 + 113868962 113868962 113868962 AAAGGAAGTCCTAGAATATACTGCAGGAGGAAAAGAGTGTGGAGAAGATACTGGAGAGATGAGAT AAAGGAAGTCCTAGAATATACTGCAGGAGGAACAGAGTGTGGAGAAGATACTGGAGAGATGAGAT A C NHLRC2 Ensembl:ENSG00000196865 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs554430775 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42738,RMVar_hsa_circ_45724,RMVar_hsa_circ_368005 30135 RMVar_ID_30135 Human_SNP_ID_447768955 A-to-I Human chr10 - 114129205 114129196 114129205 TTCCCACCTCAGCCTCTCAAGTAACCGGAACTATAGGCACTTGCCACCACGCCTAGCTAATGTTT TTCCCACCTCAGCCTCTCAAGTAACCGGAACT_________TGCCACCACGCCTAGCTAATGTTT AAGTGCCTAT A CCDC186 Ensembl:ENSG00000165813 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1262401044 Functional Loss DEL dbSNP153 33..41 33 - - - RMVar_hsa_circ_63596 30136 RMVar_ID_30136 Human_SNP_ID_447778598 A-to-I Human chr10 - 114167159 114167159 114167159 AAAATTAGCTGGGCATGGTGGCTCGTGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGA AAAATTAGCTGGGCATGGTGGCTCGTGCCTGTTATCCCAGCTACTTGGGAGGCTGAGGCAGGAGA T A CCDC186 Ensembl:ENSG00000165813 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1214974543 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63829,RMVar_hsa_circ_146452 30137 RMVar_ID_30137 Human_SNP_ID_447847166 A-to-I Human chr10 - 114434724 114434724 114434724 ATGAAACCACATCATGATTCCCGACGTGAGTTAGATGAGGGAGAGTTTGTGTAACTCCACACCCA ATGAAACCACATCATGATTCCCGACGTGAGTTGGATGAGGGAGAGTTTGTGTAACTCCACACCCA T C ABLIM1 Ensembl:ENSG00000099204 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs541053335 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4107847,Human_RBP_ID_23435885,Human_RBP_ID_24456236 RMVar_hsa_circ_92748,RMVar_hsa_circ_101355,RMVar_hsa_circ_107118,RMVar_hsa_circ_112242,RMVar_hsa_circ_122800,RMVar_hsa_circ_101470,RMVar_hsa_circ_95635,RMVar_hsa_circ_146457,RMVar_hsa_circ_146461,RMVar_hsa_circ_88888,RMVar_hsa_circ_89929,RMVar_hsa_circ_146463,RMVar_hsa_circ_86375,RMVar_hsa_circ_146462,RMVar_hsa_circ_146459,RMVar_hsa_circ_146460,RMVar_hsa_circ_146458,RMVar_hsa_circ_146455,RMVar_hsa_circ_146456,RMVar_hsa_circ_146454 30138 RMVar_ID_30138 Human_SNP_ID_447852587 A-to-I Human chr10 - 114457345 114457345 114457345 GAATCGCTTGAACCTGGGAGGCGGAGGTTACAATGAGCCGAGACTGCACCACTGCACTACAGCCT GAATCGCTTGAACCTGGGAGGCGGAGGTTACAGTGAGCCGAGACTGCACCACTGCACTACAGCCT T C ABLIM1 Ensembl:ENSG00000099204 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs943377794 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34764,RMVar_hsa_circ_107118,RMVar_hsa_circ_122800,RMVar_hsa_circ_101470,RMVar_hsa_circ_95635,RMVar_hsa_circ_146457,RMVar_hsa_circ_89929,RMVar_hsa_circ_86375,RMVar_hsa_circ_146459,RMVar_hsa_circ_146458,RMVar_hsa_circ_146455,RMVar_hsa_circ_146456,RMVar_hsa_circ_146454,RMVar_hsa_circ_20409,RMVar_hsa_circ_72075,RMVar_hsa_circ_115438,RMVar_hsa_circ_374856,RMVar_hsa_circ_146468,RMVar_hsa_circ_146466,RMVar_hsa_circ_146467,RMVar_hsa_circ_85284 30139 RMVar_ID_30139 Human_SNP_ID_447852588 A-to-I Human chr10 - 114457345 114457345 114457345 GAATCGCTTGAACCTGGGAGGCGGAGGTTACAATGAGCCGAGACTGCACCACTGCACTACAGCCT GAATCGCTTGAACCTGGGAGGCGGAGGTTACACTGAGCCGAGACTGCACCACTGCACTACAGCCT T G ABLIM1 Ensembl:ENSG00000099204 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs943377794 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34764,RMVar_hsa_circ_107118,RMVar_hsa_circ_122800,RMVar_hsa_circ_101470,RMVar_hsa_circ_95635,RMVar_hsa_circ_146457,RMVar_hsa_circ_89929,RMVar_hsa_circ_86375,RMVar_hsa_circ_146459,RMVar_hsa_circ_146458,RMVar_hsa_circ_146455,RMVar_hsa_circ_146456,RMVar_hsa_circ_146454,RMVar_hsa_circ_20409,RMVar_hsa_circ_72075,RMVar_hsa_circ_115438,RMVar_hsa_circ_374856,RMVar_hsa_circ_146468,RMVar_hsa_circ_146466,RMVar_hsa_circ_146467,RMVar_hsa_circ_85284 30140 RMVar_ID_30140 Human_SNP_ID_447852596 A-to-I Human chr10 - 114457381 114457381 114457381 TCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAACCTGGGAGGCGGAGGTT TCTGTAATCCCAGCTACTTGGGAGGCTGAGGCGGGAGAATCGCTTGAACCTGGGAGGCGGAGGTT T C ABLIM1 Ensembl:ENSG00000099204 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs777865507 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34764,RMVar_hsa_circ_107118,RMVar_hsa_circ_122800,RMVar_hsa_circ_101470,RMVar_hsa_circ_95635,RMVar_hsa_circ_146457,RMVar_hsa_circ_89929,RMVar_hsa_circ_86375,RMVar_hsa_circ_146459,RMVar_hsa_circ_146458,RMVar_hsa_circ_146455,RMVar_hsa_circ_146456,RMVar_hsa_circ_146454,RMVar_hsa_circ_20409,RMVar_hsa_circ_72075,RMVar_hsa_circ_115438,RMVar_hsa_circ_374856,RMVar_hsa_circ_146468,RMVar_hsa_circ_146466,RMVar_hsa_circ_146467,RMVar_hsa_circ_85284 30141 RMVar_ID_30141 Human_SNP_ID_447852737 A-to-I Human chr10 - 114458064 114458064 114458064 CAGAGTAGTTTTGTTTTTTGTTTTGAGGCAGAATCTCACTTTGTTGCCCCAGCTGGAGTGCAGTG CAGAGTAGTTTTGTTTTTTGTTTTGAGGCAGAGTCTCACTTTGTTGCCCCAGCTGGAGTGCAGTG T C ABLIM1 Ensembl:ENSG00000099204 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1375208364 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34764,RMVar_hsa_circ_107118,RMVar_hsa_circ_122800,RMVar_hsa_circ_101470,RMVar_hsa_circ_95635,RMVar_hsa_circ_146457,RMVar_hsa_circ_89929,RMVar_hsa_circ_86375,RMVar_hsa_circ_146459,RMVar_hsa_circ_146458,RMVar_hsa_circ_146455,RMVar_hsa_circ_146456,RMVar_hsa_circ_146454,RMVar_hsa_circ_20409,RMVar_hsa_circ_72075,RMVar_hsa_circ_115438,RMVar_hsa_circ_374856,RMVar_hsa_circ_146468,RMVar_hsa_circ_146466,RMVar_hsa_circ_146467,RMVar_hsa_circ_85284 30142 RMVar_ID_30142 Human_SNP_ID_447853303 A-to-I Human chr10 - 114460549 114460549 114460549 TTGCCCAGGCTGGCATGCAGTGGCACAATCTCAGCTCACTGCAGCCTCCGCCTCCCAGCTTCAAG TTGCCCAGGCTGGCATGCAGTGGCACAATCTCGGCTCACTGCAGCCTCCGCCTCCCAGCTTCAAG T C ABLIM1 Ensembl:ENSG00000099204 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1233612760 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34764,RMVar_hsa_circ_107118,RMVar_hsa_circ_122800,RMVar_hsa_circ_101470,RMVar_hsa_circ_95635,RMVar_hsa_circ_146457,RMVar_hsa_circ_89929,RMVar_hsa_circ_86375,RMVar_hsa_circ_146459,RMVar_hsa_circ_146458,RMVar_hsa_circ_146455,RMVar_hsa_circ_146456,RMVar_hsa_circ_146454,RMVar_hsa_circ_20409,RMVar_hsa_circ_72075,RMVar_hsa_circ_115438,RMVar_hsa_circ_374856,RMVar_hsa_circ_146468,RMVar_hsa_circ_146466,RMVar_hsa_circ_146467,RMVar_hsa_circ_85284 30143 RMVar_ID_30143 Human_SNP_ID_447853654 A-to-I Human chr10 - 114461743 114461743 114461743 GCAAACTTGGCTCACTGCAACCTCCACTTCCCAGGCTCAAGCGATTCTTATGCCTCAGCCTCCTG GCAAACTTGGCTCACTGCAACCTCCACTTCCCGGGCTCAAGCGATTCTTATGCCTCAGCCTCCTG T C ABLIM1 Ensembl:ENSG00000099204 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1389929115 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34764,RMVar_hsa_circ_107118,RMVar_hsa_circ_122800,RMVar_hsa_circ_101470,RMVar_hsa_circ_95635,RMVar_hsa_circ_146457,RMVar_hsa_circ_89929,RMVar_hsa_circ_86375,RMVar_hsa_circ_146459,RMVar_hsa_circ_146458,RMVar_hsa_circ_146455,RMVar_hsa_circ_146456,RMVar_hsa_circ_146454,RMVar_hsa_circ_20409,RMVar_hsa_circ_72075,RMVar_hsa_circ_115438,RMVar_hsa_circ_374856,RMVar_hsa_circ_146468,RMVar_hsa_circ_146466,RMVar_hsa_circ_146467,RMVar_hsa_circ_85284 30144 RMVar_ID_30144 Human_SNP_ID_447853660 A-to-I Human chr10 - 114461762 114461762 114461762 CAGGCTGGAGTACAATGGTGCAAACTTGGCTCACTGCAACCTCCACTTCCCAGGCTCAAGCGATT CAGGCTGGAGTACAATGGTGCAAACTTGGCTCGCTGCAACCTCCACTTCCCAGGCTCAAGCGATT T C ABLIM1 Ensembl:ENSG00000099204 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1490540293 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34764,RMVar_hsa_circ_107118,RMVar_hsa_circ_122800,RMVar_hsa_circ_101470,RMVar_hsa_circ_95635,RMVar_hsa_circ_146457,RMVar_hsa_circ_89929,RMVar_hsa_circ_86375,RMVar_hsa_circ_146459,RMVar_hsa_circ_146458,RMVar_hsa_circ_146455,RMVar_hsa_circ_146456,RMVar_hsa_circ_146454,RMVar_hsa_circ_20409,RMVar_hsa_circ_72075,RMVar_hsa_circ_115438,RMVar_hsa_circ_374856,RMVar_hsa_circ_146468,RMVar_hsa_circ_146466,RMVar_hsa_circ_146467,RMVar_hsa_circ_85284 30145 RMVar_ID_30145 Human_SNP_ID_447855527 A-to-I Human chr10 - 114468817 114468817 114468817 TCGATCTCCTGACCTTGTGGTCCGCCAGCCTCAGCCTCCCAAAGTGCTGGGATTACAGACGTGAG TCGATCTCCTGACCTTGTGGTCCGCCAGCCTCGGCCTCCCAAAGTGCTGGGATTACAGACGTGAG T C ABLIM1 Ensembl:ENSG00000099204 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1305015120 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34764,RMVar_hsa_circ_107118,RMVar_hsa_circ_122800,RMVar_hsa_circ_101470,RMVar_hsa_circ_146457,RMVar_hsa_circ_89929,RMVar_hsa_circ_146455,RMVar_hsa_circ_146456,RMVar_hsa_circ_146454,RMVar_hsa_circ_53410,RMVar_hsa_circ_20409,RMVar_hsa_circ_72075,RMVar_hsa_circ_115438,RMVar_hsa_circ_146466,RMVar_hsa_circ_300141,RMVar_hsa_circ_377515,RMVar_hsa_circ_283245,RMVar_hsa_circ_40012,RMVar_hsa_circ_51283,RMVar_hsa_circ_146471,RMVar_hsa_circ_359623 30146 RMVar_ID_30146 Human_SNP_ID_447855951 A-to-I Human chr10 - 114470295 114470295 114470295 CCTCAGCTTCCCAAGTAGCTGAGACTACGGGCATGTGCCACCATGCTGGGCTAATTTTTGTATTT CCTCAGCTTCCCAAGTAGCTGAGACTACGGGCTTGTGCCACCATGCTGGGCTAATTTTTGTATTT T A ABLIM1 Ensembl:ENSG00000099204 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1402620540 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34764,RMVar_hsa_circ_107118,RMVar_hsa_circ_122800,RMVar_hsa_circ_101470,RMVar_hsa_circ_146457,RMVar_hsa_circ_89929,RMVar_hsa_circ_146455,RMVar_hsa_circ_146456,RMVar_hsa_circ_146454,RMVar_hsa_circ_53410,RMVar_hsa_circ_20409,RMVar_hsa_circ_72075,RMVar_hsa_circ_115438,RMVar_hsa_circ_146466,RMVar_hsa_circ_300141,RMVar_hsa_circ_377515,RMVar_hsa_circ_283245,RMVar_hsa_circ_40012,RMVar_hsa_circ_51283,RMVar_hsa_circ_146471,RMVar_hsa_circ_359623 30147 RMVar_ID_30147 Human_SNP_ID_447863756 A-to-I Human chr10 - 114503407 114503407 114503407 TCTCTTTCTGTTCCAGGCTGGAGGGCGGTGGCATGATCACGGCTCACTGCAGCCTTGACCTCCCA TCTCTTTCTGTTCCAGGCTGGAGGGCGGTGGCGTGATCACGGCTCACTGCAGCCTTGACCTCCCA T C ABLIM1 Ensembl:ENSG00000099204 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1166924623 Functional Loss SNV dbSNP153 33..33 33 - - - 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 30148 RMVar_ID_30148 Human_SNP_ID_447867249 A-to-I Human chr10 - 114518363 114518363 114518363 GCCCATTGCATGTGGTTCAGAGAAGTACAAAGAAGTGTACTTATTCAGTTATTTATTTACAATAA GCCCATTGCATGTGGTTCAGAGAAGTACAAAGTAGTGTACTTATTCAGTTATTTATTTACAATAA T A ABLIM1 Ensembl:ENSG00000099204 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1274530496 Functional Loss SNV dbSNP153 33..33 33 - - - 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 30149 RMVar_ID_30149 Human_SNP_ID_447867250 A-to-I Human chr10 - 114518363 114518363 114518363 GCCCATTGCATGTGGTTCAGAGAAGTACAAAGAAGTGTACTTATTCAGTTATTTATTTACAATAA GCCCATTGCATGTGGTTCAGAGAAGTACAAAGCAGTGTACTTATTCAGTTATTTATTTACAATAA T G ABLIM1 Ensembl:ENSG00000099204 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1274530496 Functional Loss SNV dbSNP153 33..33 33 - - - 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 30150 RMVar_ID_30150 Human_SNP_ID_447911106 A-to-I Human chr10 - 114707339 114707339 114707339 AGTTCCAGCTACTCGGAAGGCTGAGGCTGGAGAATCGCTTGAACCTGGGAGGCAGAGATTGCAGT AGTTCCAGCTACTCGGAAGGCTGAGGCTGGAGTATCGCTTGAACCTGGGAGGCAGAGATTGCAGT T A ABLIM1 Ensembl:ENSG00000099204 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs761857002 Functional Loss SNV dbSNP153 33..33 33 - - - 30151 RMVar_ID_30151 Human_SNP_ID_447941693 A-to-I Human chr10 + 114837093 114837093 114837093 CTGGCTAATTTTTTAAGTTTTTTTGTAGAGACAGTGTCTCCCTGTGTTGTCCGGGCTGGTCTGGA CTGGCTAATTTTTTAAGTTTTTTTGTAGAGACGGTGTCTCCCTGTGTTGTCCGGGCTGGTCTGGA A G FAM160B1 Ensembl:ENSG00000151553 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs533793323 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21337,RMVar_hsa_circ_93106,RMVar_hsa_circ_330595,RMVar_hsa_circ_346280,RMVar_hsa_circ_146484,RMVar_hsa_circ_323388,RMVar_hsa_circ_64330,RMVar_hsa_circ_272523,RMVar_hsa_circ_22238,RMVar_hsa_circ_55442,RMVar_hsa_circ_146486,RMVar_hsa_circ_146488,RMVar_hsa_circ_146489,RMVar_hsa_circ_146487,RMVar_hsa_circ_331715,RMVar_hsa_circ_146491,RMVar_hsa_circ_372743 30152 RMVar_ID_30152 Human_SNP_ID_447942387 A-to-I Human chr10 + 114839716 114839716 114839716 CATCCTGGCTAACACAGTGAAACCCCTTCTCTACTAAAAATACAAAAAATCAGTCGGGCTTGGTG CATCCTGGCTAACACAGTGAAACCCCTTCTCTCCTAAAAATACAAAAAATCAGTCGGGCTTGGTG A C FAM160B1 Ensembl:ENSG00000151553 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1182615275 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8983066 RMVar_hsa_circ_21337,RMVar_hsa_circ_93106,RMVar_hsa_circ_330595,RMVar_hsa_circ_346280,RMVar_hsa_circ_146484,RMVar_hsa_circ_323388,RMVar_hsa_circ_64330,RMVar_hsa_circ_272523,RMVar_hsa_circ_22238,RMVar_hsa_circ_55442,RMVar_hsa_circ_146486,RMVar_hsa_circ_146488,RMVar_hsa_circ_146489,RMVar_hsa_circ_146487,RMVar_hsa_circ_331715,RMVar_hsa_circ_146491,RMVar_hsa_circ_372743 30153 RMVar_ID_30153 Human_SNP_ID_448005212 A-to-I Human chr10 + 115105995 115105995 115105995 TGTGAGAAGAGGGCCACTGTCCTGCAGACCCCAGAACAGTAGATGCTCCTACACCTTGCACCATG TGTGAGAAGAGGGCCACTGTCCTGCAGACCCCGGAACAGTAGATGCTCCTACACCTTGCACCATG A G ATRNL1 Ensembl:ENSG00000107518 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs556240405 Functional Loss SNV dbSNP153 33..33 33 - - - 30154 RMVar_ID_30154 Human_SNP_ID_448005285 A-to-I Human chr10 + 115106302 115106302 115106302 CCATTTGGAATGGCTGTATTTATCCAATACCTATACCCCCATTGTATCTAGGAAGTAACTAGCTT CCATTTGGAATGGCTGTATTTATCCAATACCTTTACCCCCATTGTATCTAGGAAGTAACTAGCTT A T ATRNL1 Ensembl:ENSG00000107518 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1274685929 Functional Loss SNV dbSNP153 33..33 33 - - - 30155 RMVar_ID_30155 Human_SNP_ID_448007273 A-to-I Human chr10 + 115114602 115114602 115114602 ATGGGCAAATAATCTGAATAGACATTTTTCAAAAGAAAACATACAAAAGGTCAAAACATATATGA ATGGGCAAATAATCTGAATAGACATTTTTCAACAGAAAACATACAAAAGGTCAAAACATATATGA A C ATRNL1 Ensembl:ENSG00000107518 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1463164545 Functional Loss SNV dbSNP153 33..33 33 - - - 30156 RMVar_ID_30156 Human_SNP_ID_448007299 A-to-I Human chr10 + 115114678 115114678 115114678 ACATTACTAATCATCAGGGAAATGCAGATCAAAACCACAATGGGATGTCATCTCATACCTCTTAA ACATTACTAATCATCAGGGAAATGCAGATCAATACCACAATGGGATGTCATCTCATACCTCTTAA A T ATRNL1 Ensembl:ENSG00000107518 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1026782658 Functional Loss SNV dbSNP153 33..33 33 - - - 30157 RMVar_ID_30157 Human_SNP_ID_448008066 A-to-I Human chr10 + 115117823 115117823 115117823 TGGTTGTACTAATTTACATTCCCACAAACAGTATAAGAGGGTTCCCTTTTCTCCATATCCTTGCC TGGTTGTACTAATTTACATTCCCACAAACAGTGTAAGAGGGTTCCCTTTTCTCCATATCCTTGCC A G ATRNL1 Ensembl:ENSG00000107518 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs544856279 Functional Loss SNV dbSNP153 33..33 33 - - - 30158 RMVar_ID_30158 Human_SNP_ID_448024844 A-to-I Human chr10 + 115186581 115186581 115186581 CATTTGCACCATTGATGGAACTGGAAATCATTAAGTGAAATAAGCCAGGCACAGAAAGAAAACTG CATTTGCACCATTGATGGAACTGGAAATCATTGAGTGAAATAAGCCAGGCACAGAAAGAAAACTG A G ATRNL1 Ensembl:ENSG00000107518 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1289605701 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_291,RMVar_hsa_circ_274252,RMVar_hsa_circ_301732,RMVar_hsa_circ_305885,RMVar_hsa_circ_310668,RMVar_hsa_circ_302144,RMVar_hsa_circ_297166,RMVar_hsa_circ_300493,RMVar_hsa_circ_295486,RMVar_hsa_circ_280575,RMVar_hsa_circ_287569,RMVar_hsa_circ_289675,RMVar_hsa_circ_284040,RMVar_hsa_circ_279878,RMVar_hsa_circ_276037,RMVar_hsa_circ_46228,RMVar_hsa_circ_41238,RMVar_hsa_circ_33397,RMVar_hsa_circ_25270,RMVar_hsa_circ_297011,RMVar_hsa_circ_351820,RMVar_hsa_circ_360077,RMVar_hsa_circ_327538,RMVar_hsa_circ_311410,RMVar_hsa_circ_17098,RMVar_hsa_circ_36122,RMVar_hsa_circ_5472,RMVar_hsa_circ_41798,RMVar_hsa_circ_59916,RMVar_hsa_circ_274974,RMVar_hsa_circ_311565,RMVar_hsa_circ_34140,RMVar_hsa_circ_14678,RMVar_hsa_circ_24602,RMVar_hsa_circ_12792 30159 RMVar_ID_30159 Human_SNP_ID_448026040 A-to-I Human chr10 + 115191295 115191295 115191295 TTCTATTTTTAGTTTTTTAGGAACTCCAAACTATTCTTCATAGTGGTTGTACTAATTTATGTTCT TTCTATTTTTAGTTTTTTAGGAACTCCAAACTGTTCTTCATAGTGGTTGTACTAATTTATGTTCT A G ATRNL1 Ensembl:ENSG00000107518 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1468461853 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5931571 RMVar_hsa_circ_291,RMVar_hsa_circ_274252,RMVar_hsa_circ_301732,RMVar_hsa_circ_305885,RMVar_hsa_circ_310668,RMVar_hsa_circ_302144,RMVar_hsa_circ_297166,RMVar_hsa_circ_300493,RMVar_hsa_circ_295486,RMVar_hsa_circ_280575,RMVar_hsa_circ_287569,RMVar_hsa_circ_289675,RMVar_hsa_circ_284040,RMVar_hsa_circ_279878,RMVar_hsa_circ_276037,RMVar_hsa_circ_46228,RMVar_hsa_circ_41238,RMVar_hsa_circ_33397,RMVar_hsa_circ_25270,RMVar_hsa_circ_297011,RMVar_hsa_circ_351820,RMVar_hsa_circ_360077,RMVar_hsa_circ_327538,RMVar_hsa_circ_311410,RMVar_hsa_circ_17098,RMVar_hsa_circ_36122,RMVar_hsa_circ_5472,RMVar_hsa_circ_41798,RMVar_hsa_circ_59916,RMVar_hsa_circ_274974,RMVar_hsa_circ_311565,RMVar_hsa_circ_34140,RMVar_hsa_circ_14678,RMVar_hsa_circ_24602,RMVar_hsa_circ_12792 30160 RMVar_ID_30160 Human_SNP_ID_448030803 A-to-I Human chr10 + 115209446 115209446 115209446 TTTATTTTGTTTTTTTTTTTTTCTGGTTTCTGAGTTGTTTGTGGCAGGAAGTGTTTTCTAAATTA TTTATTTTGTTTTTTTTTTTTTCTGGTTTCTGTGTTGTTTGTGGCAGGAAGTGTTTTCTAAATTA A T ATRNL1 Ensembl:ENSG00000107518 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1238554034 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_291,RMVar_hsa_circ_274252,RMVar_hsa_circ_301732,RMVar_hsa_circ_305885,RMVar_hsa_circ_310668,RMVar_hsa_circ_302144,RMVar_hsa_circ_297166,RMVar_hsa_circ_300493,RMVar_hsa_circ_295486,RMVar_hsa_circ_280575,RMVar_hsa_circ_287569,RMVar_hsa_circ_289675,RMVar_hsa_circ_284040,RMVar_hsa_circ_279878,RMVar_hsa_circ_276037,RMVar_hsa_circ_46228,RMVar_hsa_circ_41238,RMVar_hsa_circ_33397,RMVar_hsa_circ_25270,RMVar_hsa_circ_297011,RMVar_hsa_circ_351820,RMVar_hsa_circ_360077,RMVar_hsa_circ_327538,RMVar_hsa_circ_311410,RMVar_hsa_circ_17098,RMVar_hsa_circ_36122,RMVar_hsa_circ_5472,RMVar_hsa_circ_41798,RMVar_hsa_circ_59916,RMVar_hsa_circ_274974,RMVar_hsa_circ_311565,RMVar_hsa_circ_34140,RMVar_hsa_circ_14678,RMVar_hsa_circ_24602,RMVar_hsa_circ_12792 30161 RMVar_ID_30161 Human_SNP_ID_448084832 A-to-I Human chr10 + 115426794 115426794 115426794 TCGCCCAGGCTGGAGTGCAACGGCACAATCTCAGTTCACTGCAACCCCTGCCTCCCAGGTTCAAG TCGCCCAGGCTGGAGTGCAACGGCACAATCTCGGTTCACTGCAACCCCTGCCTCCCAGGTTCAAG A G ATRNL1 Ensembl:ENSG00000107518 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1296640146 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_274252,RMVar_hsa_circ_301732,RMVar_hsa_circ_310668,RMVar_hsa_circ_297166,RMVar_hsa_circ_287569,RMVar_hsa_circ_41238,RMVar_hsa_circ_360077,RMVar_hsa_circ_5472,RMVar_hsa_circ_34140,RMVar_hsa_circ_14678,RMVar_hsa_circ_322870,RMVar_hsa_circ_23037,RMVar_hsa_circ_340201,RMVar_hsa_circ_34068,RMVar_hsa_circ_31635,RMVar_hsa_circ_20179,RMVar_hsa_circ_367555,RMVar_hsa_circ_24902,RMVar_hsa_circ_14401,RMVar_hsa_circ_43943,RMVar_hsa_circ_377530,RMVar_hsa_circ_15191,RMVar_hsa_circ_26301,RMVar_hsa_circ_10731,RMVar_hsa_circ_12967,RMVar_hsa_circ_10368,RMVar_hsa_circ_4295,RMVar_hsa_circ_324861,RMVar_hsa_circ_377814,RMVar_hsa_circ_21187,RMVar_hsa_circ_41523,RMVar_hsa_circ_299033,RMVar_hsa_circ_335802,RMVar_hsa_circ_301297,RMVar_hsa_circ_277261,RMVar_hsa_circ_146523,RMVar_hsa_circ_146524,RMVar_hsa_circ_279967,RMVar_hsa_circ_310013,RMVar_hsa_circ_311358,RMVar_hsa_circ_267636,RMVar_hsa_circ_146525,RMVar_hsa_circ_146526 30162 RMVar_ID_30162 Human_SNP_ID_448130110 A-to-I Human chr10 + 115602286 115602286 115602286 TGAGGCAGGAGAATCTCTTGAACCCTGGGGTCAGAGGTTGCAGTGAGCCGAGATCATGCCACTTC TGAGGCAGGAGAATCTCTTGAACCCTGGGGTCGGAGGTTGCAGTGAGCCGAGATCATGCCACTTC A G ATRNL1 Ensembl:ENSG00000107518 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs948979149 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_301732,RMVar_hsa_circ_297166,RMVar_hsa_circ_34140,RMVar_hsa_circ_340201,RMVar_hsa_circ_24902,RMVar_hsa_circ_15191,RMVar_hsa_circ_21187,RMVar_hsa_circ_41523,RMVar_hsa_circ_335802,RMVar_hsa_circ_267636,RMVar_hsa_circ_318463,RMVar_hsa_circ_360287 30163 RMVar_ID_30163 Human_SNP_ID_448428790 A-to-I Human chr10 - 116830641 116830641 116830641 AGCCTCCCAAGTAGGTGGGACTACAGGCATGCACCACCACATCTGGCTAATTTTTGAATTTTTTT AGCCTCCCAAGTAGGTGGGACTACAGGCATGCGCCACCACATCTGGCTAATTTTTGAATTTTTTT T C HSPA12A Ensembl:ENSG00000165868 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1425741550 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102404,RMVar_hsa_circ_146557 30164 RMVar_ID_30164 Human_SNP_ID_448444497 A-to-I Human chr10 - 116896872 116896871 116896872 AACCCAGGAGGTGGAGGTTGCAGTGAGCCCAGATTGTGCCACTGCACTCCCAGCCTGGGCCACAG AACCCAGGAGGTGGAGGTTGCAGTGAGCCCAG_TTGTGCCACTGCACTCCCAGCCTGGGCCACAG AT A SHTN1 Ensembl:ENSG00000187164 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348484497 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_146558,RMVar_hsa_circ_77929,RMVar_hsa_circ_97758,RMVar_hsa_circ_146559 30165 RMVar_ID_30165 Human_SNP_ID_448444808 A-to-I Human chr10 - 116898289 116898289 116898289 TGTAGTCTTGCTGTCGCCCAGGCTGGAGTACAATGGCACGATCTTAGCTCACTGCAACCTCCGCC TGTAGTCTTGCTGTCGCCCAGGCTGGAGTACAGTGGCACGATCTTAGCTCACTGCAACCTCCGCC T C SHTN1 Ensembl:ENSG00000187164 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1333089721 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11488553 RMVar_hsa_circ_146558,RMVar_hsa_circ_77929,RMVar_hsa_circ_97758,RMVar_hsa_circ_146559 30166 RMVar_ID_30166 Human_SNP_ID_448457162 A-to-I Human chr10 + 116951257 116951257 116951257 TAAGCCTGGGAAATACAGGAACCCACATCTCTATAAAAATTTTTAAAAATCAGGCAGGCGTGGTG TAAGCCTGGGAAATACAGGAACCCACATCTCTGTAAAAATTTTTAAAAATCAGGCAGGCGTGGTG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1349169143 Functional Loss SNV dbSNP153 33..33 33 - - - 30167 RMVar_ID_30167 Human_SNP_ID_448540723 A-to-I Human chr10 - 117291024 117291024 117291024 TACACAAAAAAATACAAAAACTTGCCAGGCGTAGTGGTGCACGCCTGTAGTCCCAGCTGCTTGGG TACACAAAAAAATACAAAAACTTGCCAGGCGTTGTGGTGCACGCCTGTAGTCCCAGCTGCTTGGG T A PDZD8 Ensembl:ENSG00000165650 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs937560917 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_333593,RMVar_hsa_circ_361581,RMVar_hsa_circ_146582,RMVar_hsa_circ_146583 30168 RMVar_ID_30168 Human_SNP_ID_448540724 A-to-I Human chr10 - 117291024 117291024 117291024 TACACAAAAAAATACAAAAACTTGCCAGGCGTAGTGGTGCACGCCTGTAGTCCCAGCTGCTTGGG TACACAAAAAAATACAAAAACTTGCCAGGCGTCGTGGTGCACGCCTGTAGTCCCAGCTGCTTGGG T G PDZD8 Ensembl:ENSG00000165650 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs937560917 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_333593,RMVar_hsa_circ_361581,RMVar_hsa_circ_146582,RMVar_hsa_circ_146583 30169 RMVar_ID_30169 Human_SNP_ID_448554520 A-to-I Human chr10 - 117351839 117351839 117351839 CCTCACCTCTACAAAAAATAACTGGGTGTGGTAGCCTGCATCTGTAGTGCCAGCTACTTGGGATG CCTCACCTCTACAAAAAATAACTGGGTGTGGTGGCCTGCATCTGTAGTGCCAGCTACTTGGGATG T C PDZD8 Ensembl:ENSG00000165650 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs557009289 Functional Loss SNV dbSNP153 33..33 33 - - - 30170 RMVar_ID_30170 Human_SNP_ID_448559236 A-to-I Human chr10 - 117371938 117371938 117371938 TTTTTTTGTGTTTTTCGTTTGTTTGTTGAGACAGGATTTTGTTCGGTTGCCCAGAGCTGGAGTAC TTTTTTTGTGTTTTTCGTTTGTTTGTTGAGACCGGATTTTGTTCGGTTGCCCAGAGCTGGAGTAC T G PDZD8 Ensembl:ENSG00000165650 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270623302 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3340248,Human_RBP_ID_11273264 30171 RMVar_ID_30171 Human_SNP_ID_448587186 A-to-I Human chr10 - 117485820 117485820 117485820 TCTTTTTTTTTTTTTTTTTGAGACAGAGTCTCACTCTGTCTCCCAGGCTGGAGTGCAATAGCACG TCTTTTTTTTTTTTTTTTTGAGACAGAGTCTCGCTCTGTCTCCCAGGCTGGAGTGCAATAGCACG T C EMX2OS Ensembl:ENSG00000229847 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs371563943 Functional Loss SNV dbSNP153 33..33 33 - - - 30172 RMVar_ID_30172 Human_SNP_ID_448587187 A-to-I Human chr10 - 117485820 117485820 117485820 TCTTTTTTTTTTTTTTTTTGAGACAGAGTCTCACTCTGTCTCCCAGGCTGGAGTGCAATAGCACG TCTTTTTTTTTTTTTTTTTGAGACAGAGTCTCCCTCTGTCTCCCAGGCTGGAGTGCAATAGCACG T G EMX2OS Ensembl:ENSG00000229847 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs371563943 Functional Loss SNV dbSNP153 33..33 33 - - - 30173 RMVar_ID_30173 Human_SNP_ID_448587579 A-to-I Human chr10 - 117487393 117487393 117487393 AAACCTCATCTCTACAGAAAAATACAAAAATTAGTCAGGTGTAGTGGCGTGCACCTGTAGTCCCA AAACCTCATCTCTACAGAAAAATACAAAAATTCGTCAGGTGTAGTGGCGTGCACCTGTAGTCCCA T G EMX2OS Ensembl:ENSG00000229847 lincRNA intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs886106946 Functional Loss SNV dbSNP153 33..33 33 - - - 30174 RMVar_ID_30174 Human_SNP_ID_448959107 A-to-I Human chr10 - 119044724 119044724 119044724 CCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCGCCTGCCACCACGCCTGGCTAATTTTTTG CCTGCCTCAGCCTCCCAAGTAGCTGGGACTACGGGCGCCTGCCACCACGCCTGGCTAATTTTTTG T C EIF3A Ensembl:ENSG00000107581 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs557813589 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78605,RMVar_hsa_circ_2472,RMVar_hsa_circ_146615,RMVar_hsa_circ_146614,RMVar_hsa_circ_373255,RMVar_hsa_circ_110011,RMVar_hsa_circ_146617 30175 RMVar_ID_30175 Human_SNP_ID_448959239 A-to-I Human chr10 - 119045083 119045080 119045083 AAAATTAGTCGGGCATGGAGGCAGGCGCTTGTAGTCCTAGCTACCTGGGAGGCTAAGGCTCAAGA AAAATTAGTCGGGCATGGAGGCAGGCGCTTGT___CCTAGCTACCTGGGAGGCTAAGGCTCAAGA GACT G EIF3A Ensembl:ENSG00000107581 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1229455716 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_19476863 RMVar_hsa_circ_78605,RMVar_hsa_circ_2472,RMVar_hsa_circ_146615,RMVar_hsa_circ_146614,RMVar_hsa_circ_373255,RMVar_hsa_circ_110011,RMVar_hsa_circ_146617 30176 RMVar_ID_30176 Human_SNP_ID_448959251 A-to-I Human chr10 - 119045148 119045148 119045148 TTGAGGTCAGGAGTTCGAGACCAGCATGGCCAACATGTTGAAATCCCATCTCTACTAAAAATATA TTGAGGTCAGGAGTTCGAGACCAGCATGGCCAGCATGTTGAAATCCCATCTCTACTAAAAATATA T C EIF3A Ensembl:ENSG00000107581 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1248815066 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78605,RMVar_hsa_circ_2472,RMVar_hsa_circ_146615,RMVar_hsa_circ_146614,RMVar_hsa_circ_373255,RMVar_hsa_circ_110011,RMVar_hsa_circ_146617 30177 RMVar_ID_30177 Human_SNP_ID_448959422 A-to-I Human chr10 - 119045842 119045842 119045842 ATCTGCTGGGCCGGGCACATTGGTTCACGCCTATAATCTCAGCACTTTGGGAGACCGAGGCAGGC ATCTGCTGGGCCGGGCACATTGGTTCACGCCTGTAATCTCAGCACTTTGGGAGACCGAGGCAGGC T C EIF3A Ensembl:ENSG00000107581 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs926097516 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22566803 RMVar_hsa_circ_78605,RMVar_hsa_circ_2472,RMVar_hsa_circ_146615,RMVar_hsa_circ_146614,RMVar_hsa_circ_373255,RMVar_hsa_circ_110011,RMVar_hsa_circ_146617 30178 RMVar_ID_30178 Human_SNP_ID_448960150 A-to-I Human chr10 - 119048942 119048942 119048942 CATCGTTTGGCCGGGCGTGGTGGCTCATGCCTATAATTCCCAGCACTTTGGGAAGCCGAGGCGTG CATCGTTTGGCCGGGCGTGGTGGCTCATGCCTGTAATTCCCAGCACTTTGGGAAGCCGAGGCGTG T C EIF3A Ensembl:ENSG00000107581 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs759471307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11278555,Human_RBP_ID_24855727 RMVar_hsa_circ_78605,RMVar_hsa_circ_2472,RMVar_hsa_circ_146615,RMVar_hsa_circ_146614,RMVar_hsa_circ_373255,RMVar_hsa_circ_110011,RMVar_hsa_circ_146617 30179 RMVar_ID_30179 Human_SNP_ID_448960151 A-to-I Human chr10 - 119048942 119048942 119048942 CATCGTTTGGCCGGGCGTGGTGGCTCATGCCTATAATTCCCAGCACTTTGGGAAGCCGAGGCGTG CATCGTTTGGCCGGGCGTGGTGGCTCATGCCTCTAATTCCCAGCACTTTGGGAAGCCGAGGCGTG T G EIF3A Ensembl:ENSG00000107581 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs759471307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11278555,Human_RBP_ID_24855727 RMVar_hsa_circ_78605,RMVar_hsa_circ_2472,RMVar_hsa_circ_146615,RMVar_hsa_circ_146614,RMVar_hsa_circ_373255,RMVar_hsa_circ_110011,RMVar_hsa_circ_146617 30180 RMVar_ID_30180 Human_SNP_ID_448960152 A-to-I Human chr10 - 119048948 119048948 119048948 AGACATCATCGTTTGGCCGGGCGTGGTGGCTCATGCCTATAATTCCCAGCACTTTGGGAAGCCGA AGACATCATCGTTTGGCCGGGCGTGGTGGCTCGTGCCTATAATTCCCAGCACTTTGGGAAGCCGA T C EIF3A Ensembl:ENSG00000107581 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs988390494 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11278556 RMVar_hsa_circ_78605,RMVar_hsa_circ_2472,RMVar_hsa_circ_146615,RMVar_hsa_circ_146614,RMVar_hsa_circ_373255,RMVar_hsa_circ_110011,RMVar_hsa_circ_146617 30181 RMVar_ID_30181 Human_SNP_ID_448960388 A-to-I Human chr10 - 119049652 119049652 119049652 CAGCCCCCGGGTTCAAGTGATTCTCGTGTCTCAGCCTCCTGAGTAGCTGAGATTACAGGTGCATA CAGCCCCCGGGTTCAAGTGATTCTCGTGTCTCGGCCTCCTGAGTAGCTGAGATTACAGGTGCATA T C EIF3A Ensembl:ENSG00000107581 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1362237277 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18587962 RMVar_hsa_circ_78605,RMVar_hsa_circ_2472,RMVar_hsa_circ_146615,RMVar_hsa_circ_146614,RMVar_hsa_circ_373255,RMVar_hsa_circ_110011,RMVar_hsa_circ_146617 30182 RMVar_ID_30182 Human_SNP_ID_448961515 A-to-I Human chr10 - 119053601 119053601 119053601 CCCACTTCAGCCTCCTGAGTAGCTGCGACCACAGGCATGCACCACCATGCCTAGCTTTTTTTTTT CCCACTTCAGCCTCCTGAGTAGCTGCGACCACGGGCATGCACCACCATGCCTAGCTTTTTTTTTT T C EIF3A Ensembl:ENSG00000107581 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs895172734 Functional Loss SNV dbSNP153 33..33 33 - - - 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_66089,RMVar_hsa_circ_146619,RMVar_hsa_circ_366706,RMVar_hsa_circ_371542,RMVar_hsa_circ_365659,RMVar_hsa_circ_308973,RMVar_hsa_circ_337523,RMVar_hsa_circ_146624,RMVar_hsa_circ_146621,RMVar_hsa_circ_146622 30183 RMVar_ID_30183 Human_SNP_ID_448961516 A-to-I Human chr10 - 119053603 119053603 119053603 TGCCCACTTCAGCCTCCTGAGTAGCTGCGACCACAGGCATGCACCACCATGCCTAGCTTTTTTTT TGCCCACTTCAGCCTCCTGAGTAGCTGCGACCGCAGGCATGCACCACCATGCCTAGCTTTTTTTT T C EIF3A Ensembl:ENSG00000107581 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs751887665 Functional Loss SNV dbSNP153 33..33 33 - - - 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_66089,RMVar_hsa_circ_146619,RMVar_hsa_circ_366706,RMVar_hsa_circ_371542,RMVar_hsa_circ_365659,RMVar_hsa_circ_308973,RMVar_hsa_circ_337523,RMVar_hsa_circ_146624,RMVar_hsa_circ_146621,RMVar_hsa_circ_146622 30184 RMVar_ID_30184 Human_SNP_ID_448961548 A-to-I Human chr10 - 119053701 119053701 119053701 TCTTACTTTTTTGAGAGACAGGGTCTCACTCTATCACCCAGGCTGGAGTGCAGTGGCGTGATCTC TCTTACTTTTTTGAGAGACAGGGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGCGTGATCTC T C EIF3A Ensembl:ENSG00000107581 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs932339189 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_191995 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_66089,RMVar_hsa_circ_146619,RMVar_hsa_circ_366706,RMVar_hsa_circ_371542,RMVar_hsa_circ_365659,RMVar_hsa_circ_308973,RMVar_hsa_circ_337523,RMVar_hsa_circ_146624,RMVar_hsa_circ_146621,RMVar_hsa_circ_146622 30185 RMVar_ID_30185 Human_SNP_ID_448961968 A-to-I Human chr10 - 119055163 119055163 119055163 TTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCAATCTCGGCACACTGCAACCTCTGCCCCCGCCGG TTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCAGTCTCGGCACACTGCAACCTCTGCCCCCGCCGG T C EIF3A Ensembl:ENSG00000107581 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1006380568 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_191997 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_66089,RMVar_hsa_circ_146619,RMVar_hsa_circ_366706,RMVar_hsa_circ_371542,RMVar_hsa_circ_365659,RMVar_hsa_circ_308973,RMVar_hsa_circ_337523,RMVar_hsa_circ_146624,RMVar_hsa_circ_146621,RMVar_hsa_circ_146622 30186 RMVar_ID_30186 Human_SNP_ID_448964043 A-to-I Human chr10 - 119062876 119062876 119062876 GGGCATTGTGGTGCATGCGTGTAATCCCAGCTAATCGGGAGGCTGAGGCAGGAGAATCGCTTGAA GGGCATTGTGGTGCATGCGTGTAATCCCAGCTCATCGGGAGGCTGAGGCAGGAGAATCGCTTGAA T G EIF3A Ensembl:ENSG00000107581 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1387155664 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_148,RMVar_hsa_circ_78605,RMVar_hsa_circ_146614,RMVar_hsa_circ_62931,RMVar_hsa_circ_146623,RMVar_hsa_circ_354380,RMVar_hsa_circ_371542,RMVar_hsa_circ_337523,RMVar_hsa_circ_146624,RMVar_hsa_circ_361372,RMVar_hsa_circ_57897,RMVar_hsa_circ_47439,RMVar_hsa_circ_43657,RMVar_hsa_circ_8315,RMVar_hsa_circ_146628,RMVar_hsa_circ_117679,RMVar_hsa_circ_146631,RMVar_hsa_circ_146630,RMVar_hsa_circ_374213,RMVar_hsa_circ_53838 30187 RMVar_ID_30187 Human_SNP_ID_448964318 A-to-I Human chr10 - 119064003 119064003 119064003 GCGATTTCAGTTCACTGTAACCCCCACCTCCCAGGTTCAAGTGATTCTCCTACCTCAGCCTCCCA GCGATTTCAGTTCACTGTAACCCCCACCTCCCGGGTTCAAGTGATTCTCCTACCTCAGCCTCCCA T C EIF3A Ensembl:ENSG00000107581 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1400914596 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_148,RMVar_hsa_circ_78605,RMVar_hsa_circ_146614,RMVar_hsa_circ_62931,RMVar_hsa_circ_146623,RMVar_hsa_circ_354380,RMVar_hsa_circ_371542,RMVar_hsa_circ_337523,RMVar_hsa_circ_146624,RMVar_hsa_circ_361372,RMVar_hsa_circ_57897,RMVar_hsa_circ_47439,RMVar_hsa_circ_43657,RMVar_hsa_circ_8315,RMVar_hsa_circ_146628,RMVar_hsa_circ_117679,RMVar_hsa_circ_146631,RMVar_hsa_circ_146630,RMVar_hsa_circ_374213,RMVar_hsa_circ_53838 30188 RMVar_ID_30188 Human_SNP_ID_448964325 A-to-I Human chr10 - 119064016 119064016 119064016 GGAGTGCAGTGGTGCGATTTCAGTTCACTGTAACCCCCACCTCCCAGGTTCAAGTGATTCTCCTA GGAGTGCAGTGGTGCGATTTCAGTTCACTGTAGCCCCCACCTCCCAGGTTCAAGTGATTCTCCTA T C EIF3A Ensembl:ENSG00000107581 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1172149448 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_148,RMVar_hsa_circ_78605,RMVar_hsa_circ_146614,RMVar_hsa_circ_62931,RMVar_hsa_circ_146623,RMVar_hsa_circ_354380,RMVar_hsa_circ_371542,RMVar_hsa_circ_337523,RMVar_hsa_circ_146624,RMVar_hsa_circ_361372,RMVar_hsa_circ_57897,RMVar_hsa_circ_47439,RMVar_hsa_circ_43657,RMVar_hsa_circ_8315,RMVar_hsa_circ_146628,RMVar_hsa_circ_117679,RMVar_hsa_circ_146631,RMVar_hsa_circ_146630,RMVar_hsa_circ_374213,RMVar_hsa_circ_53838 30189 RMVar_ID_30189 Human_SNP_ID_448964581 A-to-I Human chr10 - 119064903 119064903 119064903 GAATTCAAGACCAGCCTGGCAAACATGGCGAAACCCGGTCTCTCCTAAAAATAACAAAAAATTAG GAATTCAAGACCAGCCTGGCAAACATGGCGAACCCCGGTCTCTCCTAAAAATAACAAAAAATTAG T G EIF3A Ensembl:ENSG00000107581 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878857134 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24786256 RMVar_hsa_circ_148,RMVar_hsa_circ_78605,RMVar_hsa_circ_146614,RMVar_hsa_circ_62931,RMVar_hsa_circ_146623,RMVar_hsa_circ_354380,RMVar_hsa_circ_371542,RMVar_hsa_circ_337523,RMVar_hsa_circ_146624,RMVar_hsa_circ_361372,RMVar_hsa_circ_57897,RMVar_hsa_circ_47439,RMVar_hsa_circ_43657,RMVar_hsa_circ_8315,RMVar_hsa_circ_146628,RMVar_hsa_circ_117679,RMVar_hsa_circ_146631,RMVar_hsa_circ_146630,RMVar_hsa_circ_374213,RMVar_hsa_circ_53838 30190 RMVar_ID_30190 Human_SNP_ID_448964999 A-to-I Human chr10 - 119066110 119066110 119066110 CTTTTTCTTTCTTTTTTTTTCTTTTTTGAGACAGAGTCTGGCTCTGTCGCCCAGGCTGGAGTGCA CTTTTTCTTTCTTTTTTTTTCTTTTTTGAGACGGAGTCTGGCTCTGTCGCCCAGGCTGGAGTGCA T C EIF3A Ensembl:ENSG00000107581 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs540687793 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6029592 RMVar_hsa_circ_78605,RMVar_hsa_circ_146614,RMVar_hsa_circ_146623,RMVar_hsa_circ_354380,RMVar_hsa_circ_371542,RMVar_hsa_circ_337523,RMVar_hsa_circ_146624,RMVar_hsa_circ_361372,RMVar_hsa_circ_57897,RMVar_hsa_circ_47439,RMVar_hsa_circ_8315,RMVar_hsa_circ_146628,RMVar_hsa_circ_117679,RMVar_hsa_circ_146631,RMVar_hsa_circ_146630,RMVar_hsa_circ_374213,RMVar_hsa_circ_300687,RMVar_hsa_circ_53838,RMVar_hsa_circ_369485,RMVar_hsa_circ_319131,RMVar_hsa_circ_61020,RMVar_hsa_circ_271170,RMVar_hsa_circ_146635,RMVar_hsa_circ_146636 30191 RMVar_ID_30191 Human_SNP_ID_448965479 A-to-I Human chr10 - 119067567 119067567 119067567 TCCTTTCTCATAGGGTCTTGCTTCCTTGCTCCAGATGGAGTGTAGTAGTGTGTTGTAGCTCACTG TCCTTTCTCATAGGGTCTTGCTTCCTTGCTCCTGATGGAGTGTAGTAGTGTGTTGTAGCTCACTG T A EIF3A Ensembl:ENSG00000107581 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10749284 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19477061 GWAS_ID_3251,GWAS_ID_3252 RMVar_hsa_circ_78605,RMVar_hsa_circ_146614,RMVar_hsa_circ_146623,RMVar_hsa_circ_354380,RMVar_hsa_circ_371542,RMVar_hsa_circ_337523,RMVar_hsa_circ_146624,RMVar_hsa_circ_361372,RMVar_hsa_circ_57897,RMVar_hsa_circ_47439,RMVar_hsa_circ_8315,RMVar_hsa_circ_146628,RMVar_hsa_circ_117679,RMVar_hsa_circ_146631,RMVar_hsa_circ_146630,RMVar_hsa_circ_374213,RMVar_hsa_circ_300687,RMVar_hsa_circ_53838,RMVar_hsa_circ_369485,RMVar_hsa_circ_319131,RMVar_hsa_circ_61020,RMVar_hsa_circ_271170,RMVar_hsa_circ_146635,RMVar_hsa_circ_146636 30192 RMVar_ID_30192 Human_SNP_ID_448965480 A-to-I Human chr10 - 119067567 119067567 119067567 TCCTTTCTCATAGGGTCTTGCTTCCTTGCTCCAGATGGAGTGTAGTAGTGTGTTGTAGCTCACTG TCCTTTCTCATAGGGTCTTGCTTCCTTGCTCCGGATGGAGTGTAGTAGTGTGTTGTAGCTCACTG T C EIF3A Ensembl:ENSG00000107581 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10749284 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19477061 GWAS_ID_3251,GWAS_ID_3252 RMVar_hsa_circ_78605,RMVar_hsa_circ_146614,RMVar_hsa_circ_146623,RMVar_hsa_circ_354380,RMVar_hsa_circ_371542,RMVar_hsa_circ_337523,RMVar_hsa_circ_146624,RMVar_hsa_circ_361372,RMVar_hsa_circ_57897,RMVar_hsa_circ_47439,RMVar_hsa_circ_8315,RMVar_hsa_circ_146628,RMVar_hsa_circ_117679,RMVar_hsa_circ_146631,RMVar_hsa_circ_146630,RMVar_hsa_circ_374213,RMVar_hsa_circ_300687,RMVar_hsa_circ_53838,RMVar_hsa_circ_369485,RMVar_hsa_circ_319131,RMVar_hsa_circ_61020,RMVar_hsa_circ_271170,RMVar_hsa_circ_146635,RMVar_hsa_circ_146636 30193 RMVar_ID_30193 Human_SNP_ID_448965481 A-to-I Human chr10 - 119067567 119067567 119067567 TCCTTTCTCATAGGGTCTTGCTTCCTTGCTCCAGATGGAGTGTAGTAGTGTGTTGTAGCTCACTG TCCTTTCTCATAGGGTCTTGCTTCCTTGCTCCCGATGGAGTGTAGTAGTGTGTTGTAGCTCACTG T G EIF3A Ensembl:ENSG00000107581 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10749284 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19477061 GWAS_ID_3251,GWAS_ID_3252 RMVar_hsa_circ_78605,RMVar_hsa_circ_146614,RMVar_hsa_circ_146623,RMVar_hsa_circ_354380,RMVar_hsa_circ_371542,RMVar_hsa_circ_337523,RMVar_hsa_circ_146624,RMVar_hsa_circ_361372,RMVar_hsa_circ_57897,RMVar_hsa_circ_47439,RMVar_hsa_circ_8315,RMVar_hsa_circ_146628,RMVar_hsa_circ_117679,RMVar_hsa_circ_146631,RMVar_hsa_circ_146630,RMVar_hsa_circ_374213,RMVar_hsa_circ_300687,RMVar_hsa_circ_53838,RMVar_hsa_circ_369485,RMVar_hsa_circ_319131,RMVar_hsa_circ_61020,RMVar_hsa_circ_271170,RMVar_hsa_circ_146635,RMVar_hsa_circ_146636 30194 RMVar_ID_30194 Human_SNP_ID_448965633 A-to-I Human chr10 - 119068101 119068101 119068101 CTTAAAAAAAAAATACATTTCTGGCCTGGCGCAGTGACTCATGTCTGTAATCCCAGCAGTTTCGG CTTAAAAAAAAAATACATTTCTGGCCTGGCGCGGTGACTCATGTCTGTAATCCCAGCAGTTTCGG T C EIF3A Ensembl:ENSG00000107581 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs954017433 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11279212 RMVar_hsa_circ_78605,RMVar_hsa_circ_146614,RMVar_hsa_circ_146623,RMVar_hsa_circ_354380,RMVar_hsa_circ_371542,RMVar_hsa_circ_337523,RMVar_hsa_circ_146624,RMVar_hsa_circ_361372,RMVar_hsa_circ_57897,RMVar_hsa_circ_47439,RMVar_hsa_circ_8315,RMVar_hsa_circ_146628,RMVar_hsa_circ_117679,RMVar_hsa_circ_146631,RMVar_hsa_circ_146630,RMVar_hsa_circ_374213,RMVar_hsa_circ_300687,RMVar_hsa_circ_53838,RMVar_hsa_circ_369485,RMVar_hsa_circ_319131,RMVar_hsa_circ_61020,RMVar_hsa_circ_271170,RMVar_hsa_circ_146635,RMVar_hsa_circ_146636 30195 RMVar_ID_30195 Human_SNP_ID_448966983 A-to-I Human chr10 - 119072525 119072525 119072525 TCGCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCCAGGATGGCACTGTTGCACTCCAGCCTTGG TCGCTTGAACCCAGGAGGCGGAGGTTGCAGTGCGCCAGGATGGCACTGTTGCACTCCAGCCTTGG T G EIF3A Ensembl:ENSG00000107581 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1382775287 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11279388,Human_RBP_ID_17559214 RMVar_hsa_circ_146623,RMVar_hsa_circ_354380,RMVar_hsa_circ_371542,RMVar_hsa_circ_337523,RMVar_hsa_circ_146624,RMVar_hsa_circ_57897,RMVar_hsa_circ_8315,RMVar_hsa_circ_117679,RMVar_hsa_circ_146631,RMVar_hsa_circ_146630,RMVar_hsa_circ_374213,RMVar_hsa_circ_53838,RMVar_hsa_circ_369485,RMVar_hsa_circ_61020,RMVar_hsa_circ_271170,RMVar_hsa_circ_146635,RMVar_hsa_circ_146636,RMVar_hsa_circ_146639,RMVar_hsa_circ_325127,RMVar_hsa_circ_146638,RMVar_hsa_circ_303037,RMVar_hsa_circ_311350,RMVar_hsa_circ_352849 30196 RMVar_ID_30196 Human_SNP_ID_448967007 A-to-I Human chr10 - 119072617 119072617 119072617 AGCCCCTTCTCTACTAAAAATACAAAAAATTTAGCCGGGCGTGGTGGTGTATGCCTGTAATCCCA AGCCCCTTCTCTACTAAAAATACAAAAAATTTGGCCGGGCGTGGTGGTGTATGCCTGTAATCCCA T C EIF3A Ensembl:ENSG00000107581 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1324403413 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_146623,RMVar_hsa_circ_354380,RMVar_hsa_circ_371542,RMVar_hsa_circ_337523,RMVar_hsa_circ_146624,RMVar_hsa_circ_57897,RMVar_hsa_circ_8315,RMVar_hsa_circ_117679,RMVar_hsa_circ_146631,RMVar_hsa_circ_146630,RMVar_hsa_circ_374213,RMVar_hsa_circ_53838,RMVar_hsa_circ_369485,RMVar_hsa_circ_61020,RMVar_hsa_circ_271170,RMVar_hsa_circ_146635,RMVar_hsa_circ_146636,RMVar_hsa_circ_146639,RMVar_hsa_circ_325127,RMVar_hsa_circ_146638,RMVar_hsa_circ_303037,RMVar_hsa_circ_311350,RMVar_hsa_circ_352849 30197 RMVar_ID_30197 Human_SNP_ID_448967036 A-to-I Human chr10 - 119072734 119072734 119072734 TTAAATGACTGCGGCCGGATGTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGTCAAGGT TTAAATGACTGCGGCCGGATGTGGTGGCTCACCCCTGTAATCCCAGCACTTTGGGAGGTCAAGGT T G EIF3A Ensembl:ENSG00000107581 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968238482 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_146623,RMVar_hsa_circ_354380,RMVar_hsa_circ_371542,RMVar_hsa_circ_337523,RMVar_hsa_circ_146624,RMVar_hsa_circ_57897,RMVar_hsa_circ_8315,RMVar_hsa_circ_117679,RMVar_hsa_circ_146631,RMVar_hsa_circ_146630,RMVar_hsa_circ_374213,RMVar_hsa_circ_53838,RMVar_hsa_circ_369485,RMVar_hsa_circ_61020,RMVar_hsa_circ_271170,RMVar_hsa_circ_146635,RMVar_hsa_circ_146636,RMVar_hsa_circ_146639,RMVar_hsa_circ_325127,RMVar_hsa_circ_146638,RMVar_hsa_circ_303037,RMVar_hsa_circ_311350,RMVar_hsa_circ_352849 30198 RMVar_ID_30198 Human_SNP_ID_448967453 A-to-I Human chr10 - 119074299 119074299 119074299 CACCACGCCTGGCTAATTTTTGTATTTTTGGTAGGGATGGGTTTCACCGTATTGGCCAGGCTGGT CACCACGCCTGGCTAATTTTTGTATTTTTGGTGGGGATGGGTTTCACCGTATTGGCCAGGCTGGT T C EIF3A Ensembl:ENSG00000107581 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs966625656 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5935623,Human_RBP_ID_11279447,Human_RBP_ID_17559545 RMVar_hsa_circ_117679,RMVar_hsa_circ_146630 30199 RMVar_ID_30199 Human_SNP_ID_448967615 A-to-I Human chr10 - 119074771 119074771 119074771 GCACCACTACGCCCTGCTAATTTTGTATTTTTAGTAGAGACTTGGTTTCTCCATTTTGGTTAGGC GCACCACTACGCCCTGCTAATTTTGTATTTTTGGTAGAGACTTGGTTTCTCCATTTTGGTTAGGC T C EIF3A Ensembl:ENSG00000107581 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1453488162 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117679,RMVar_hsa_circ_146630 30200 RMVar_ID_30200 Human_SNP_ID_448967789 A-to-I Human chr10 - 119075099 119075099 119075099 AAATTAGCCGGGCCCTGTGGTGGGTGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAA AAATTAGCCGGGCCCTGTGGTGGGTGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAA T C EIF3A Ensembl:ENSG00000107581 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1490596538 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117679,RMVar_hsa_circ_146630 30201 RMVar_ID_30201 Human_SNP_ID_448967793 A-to-I Human chr10 - 119075126 119075126 119075126 GATACCCTGTCTGTACTAAACATACAAAAATTAGCCGGGCCCTGTGGTGGGTGCCTGTAATCCCA GATACCCTGTCTGTACTAAACATACAAAAATTGGCCGGGCCCTGTGGTGGGTGCCTGTAATCCCA T C EIF3A Ensembl:ENSG00000107581 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1222204301 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117679,RMVar_hsa_circ_146630 30202 RMVar_ID_30202 Human_SNP_ID_448968273 A-to-I Human chr10 - 119076225 119076225 119076225 GAATTCAAGTAATTGTCTTGCCTCAGCCTCCCAAGTAGCTAGGATTACGGGCGTGCATCACCATG GAATTCAAGTAATTGTCTTGCCTCAGCCTCCCGAGTAGCTAGGATTACGGGCGTGCATCACCATG T C EIF3A Ensembl:ENSG00000107581 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1296352223 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117679,RMVar_hsa_circ_146630 30203 RMVar_ID_30203 Human_SNP_ID_448968504 A-to-I Human chr10 - 119076917 119076915 119076917 TTTTTTTTTTTTGAGACAGAGTCTCTCCCTCTATTGCCCAGGCTGGAGTGCAGTGACGCAATCTT TTTTTTTTTTTTGAGACAGAGTCTCTCCCTCT__TGCCCAGGCTGGAGTGCAGTGACGCAATCTT AAT A EIF3A Ensembl:ENSG00000107581 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1310300966 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_117679,RMVar_hsa_circ_146630 30204 RMVar_ID_30204 Human_SNP_ID_448968505 A-to-I Human chr10 - 119076917 119076917 119076917 TTTTTTTTTTTTGAGACAGAGTCTCTCCCTCTATTGCCCAGGCTGGAGTGCAGTGACGCAATCTT TTTTTTTTTTTTGAGACAGAGTCTCTCCCTCTGTTGCCCAGGCTGGAGTGCAGTGACGCAATCTT T C EIF3A Ensembl:ENSG00000107581 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1429564064 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117679,RMVar_hsa_circ_146630 30205 RMVar_ID_30205 Human_SNP_ID_448968826 A-to-I Human chr10 - 119077826 119077826 119077826 AGAGGAGGCCGGGCGTGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAAGCGGGTGG AGAGGAGGCCGGGCGTGGTGGCTCATGCCTGTGATCCCAGCACTTTGGGAGGCCGAAGCGGGTGG T C EIF3A Ensembl:ENSG00000107581 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1463724657 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117679,RMVar_hsa_circ_146630 30206 RMVar_ID_30206 Human_SNP_ID_448968925 A-to-I Human chr10 - 119078225 119078225 119078225 ATTTGGAGAAGGCCCCTTTTTCATATTATATCATTAGTGGTGCCACACTAACTGCTGCTGACCTT ATTTGGAGAAGGCCCCTTTTTCATATTATATCTTTAGTGGTGCCACACTAACTGCTGCTGACCTT T A EIF3A Ensembl:ENSG00000107581 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10749285 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117679,RMVar_hsa_circ_146630 30207 RMVar_ID_30207 Human_SNP_ID_448968926 A-to-I Human chr10 - 119078225 119078225 119078225 ATTTGGAGAAGGCCCCTTTTTCATATTATATCATTAGTGGTGCCACACTAACTGCTGCTGACCTT ATTTGGAGAAGGCCCCTTTTTCATATTATATCGTTAGTGGTGCCACACTAACTGCTGCTGACCTT T C EIF3A Ensembl:ENSG00000107581 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10749285 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117679,RMVar_hsa_circ_146630 30208 RMVar_ID_30208 Human_SNP_ID_448976441 A-to-I Human chr10 + 119105374 119105374 119105374 CAGTAGCGCAATCATCGCTCTCTGCAGCCTCCACCTCCCAGGCCCAAACCATCCTCCCGCCTCGG CAGTAGCGCAATCATCGCTCTCTGCAGCCTCCGCCTCCCAGGCCCAAACCATCCTCCCGCCTCGG A G DENND10 Ensembl:ENSG00000119979 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,31158229,31158229,32596459 RNA-Seq:(High) rs985833299 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1181022,Human_Splice_Rec_1181028,Human_Splice_Rec_1181074 30209 RMVar_ID_30209 Human_SNP_ID_448976443 A-to-I Human chr10 + 119105381 119105381 119105381 GCAATCATCGCTCTCTGCAGCCTCCACCTCCCAGGCCCAAACCATCCTCCCGCCTCGGCCTCCGA GCAATCATCGCTCTCTGCAGCCTCCACCTCCCGGGCCCAAACCATCCTCCCGCCTCGGCCTCCGA A G DENND10 Ensembl:ENSG00000119979 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1428204915 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1181022,Human_Splice_Rec_1181028,Human_Splice_Rec_1181074 30210 RMVar_ID_30210 Human_SNP_ID_448976882 A-to-I Human chr10 + 119107218 119107218 119107218 GGGCACCTGTAATCCCAGCTACTTGGGAGGCCAAGGCAGAAGAATCGTTTGAACCTGGGAGCCAA GGGCACCTGTAATCCCAGCTACTTGGGAGGCCGAGGCAGAAGAATCGTTTGAACCTGGGAGCCAA A G DENND10 Ensembl:ENSG00000119979 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985428230 Functional Loss SNV dbSNP153 33..33 33 - - - 30211 RMVar_ID_30211 Human_SNP_ID_448977774 A-to-I Human chr10 + 119110477 119110477 119110477 TATAAGTAAATGAAGGTTTTTTTCTTTTTTTGAGACAAAGTCTCACTCTGTCGCCCAGCCTGGAG TATAAGTAAATGAAGGTTTTTTTCTTTTTTTGTGACAAAGTCTCACTCTGTCGCCCAGCCTGGAG A T DENND10 Ensembl:ENSG00000119979 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1461728973 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12235,RMVar_hsa_circ_146646,RMVar_hsa_circ_308245,RMVar_hsa_circ_309090,RMVar_hsa_circ_343446,RMVar_hsa_circ_308642,RMVar_hsa_circ_278156,RMVar_hsa_circ_296284,RMVar_hsa_circ_146647,RMVar_hsa_circ_120350,RMVar_hsa_circ_317399,RMVar_hsa_circ_146645,RMVar_hsa_circ_349410,RMVar_hsa_circ_302793,RMVar_hsa_circ_69305,RMVar_hsa_circ_146648 30212 RMVar_ID_30212 Human_SNP_ID_448981360 A-to-I Human chr10 + 119124589 119124589 119124589 CCTTTTTTTTTGAGACCAGGTCTTCCTGTGTTACTCAGGCTGGTCTTGAACTCCCGAACTCAAGC CCTTTTTTTTTGAGACCAGGTCTTCCTGTGTTGCTCAGGCTGGTCTTGAACTCCCGAACTCAAGC A G DENND10 Ensembl:ENSG00000119979 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1029239017 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_309090,RMVar_hsa_circ_278156,RMVar_hsa_circ_146647,RMVar_hsa_circ_120350,RMVar_hsa_circ_69305,RMVar_hsa_circ_146648,RMVar_hsa_circ_32092,RMVar_hsa_circ_146652,RMVar_hsa_circ_339681 30213 RMVar_ID_30213 Human_SNP_ID_448987776 A-to-I Human chr10 - 119149347 119149347 119149347 CGTGACTGTCACCCACAGCAGGGCAGAGGTGCAAGCAGAGAGCAGGGGCCGGGTGGTAGGAGGAG CGTGACTGTCACCCACAGCAGGGCAGAGGTGCGAGCAGAGAGCAGGGGCCGGGTGGTAGGAGGAG T C SFXN4 Ensembl:ENSG00000183605 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7089432 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4908,RMVar_hsa_circ_47601,RMVar_hsa_circ_377819,RMVar_hsa_circ_146654,RMVar_hsa_circ_13049 30214 RMVar_ID_30214 Human_SNP_ID_448988105 A-to-I Human chr10 - 119150630 119150630 119150630 GAGTCTCCCTCTGTTGCCAAAGCTGGAGGGCAATGGTACGAACATGGCTCACTGCAGCCTCAACT GAGTCTCCCTCTGTTGCCAAAGCTGGAGGGCAGTGGTACGAACATGGCTCACTGCAGCCTCAACT T C SFXN4 Ensembl:ENSG00000183605 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1262616229 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4908,RMVar_hsa_circ_47601,RMVar_hsa_circ_377819,RMVar_hsa_circ_146654,RMVar_hsa_circ_13049 30215 RMVar_ID_30215 Human_SNP_ID_448991534 A-to-I Human chr10 - 119163575 119163575 119163575 AACATGGTGAAACCGACGTCTCTACTAAAAATACAAACATTAGCTGGGTGTGGTGGCAGACACCT AACATGGTGAAACCGACGTCTCTACTAAAAATGCAAACATTAGCTGGGTGTGGTGGCAGACACCT T C SFXN4 Ensembl:ENSG00000183605 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs569920017 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13049,RMVar_hsa_circ_83195,RMVar_hsa_circ_49112,RMVar_hsa_circ_269372,RMVar_hsa_circ_146661 30216 RMVar_ID_30216 Human_SNP_ID_448991535 A-to-I Human chr10 - 119163584 119163584 119163584 AGCCTGACCAACATGGTGAAACCGACGTCTCTACTAAAAATACAAACATTAGCTGGGTGTGGTGG AGCCTGACCAACATGGTGAAACCGACGTCTCTTCTAAAAATACAAACATTAGCTGGGTGTGGTGG T A SFXN4 Ensembl:ENSG00000183605 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1224720482 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13049,RMVar_hsa_circ_83195,RMVar_hsa_circ_49112,RMVar_hsa_circ_269372,RMVar_hsa_circ_146661 30217 RMVar_ID_30217 Human_SNP_ID_448991542 A-to-I Human chr10 - 119163596 119163596 119163596 GAATTCGAGACCAGCCTGACCAACATGGTGAAACCGACGTCTCTACTAAAAATACAAACATTAGC GAATTCGAGACCAGCCTGACCAACATGGTGAAGCCGACGTCTCTACTAAAAATACAAACATTAGC T C SFXN4 Ensembl:ENSG00000183605 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1257537758 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13049,RMVar_hsa_circ_83195,RMVar_hsa_circ_49112,RMVar_hsa_circ_269372,RMVar_hsa_circ_146661 30218 RMVar_ID_30218 Human_SNP_ID_448991624 A-to-I Human chr10 - 119163884 119163884 119163884 AGGCATGCGCCACCATGCCCGGCTAATTTTGTATTTTTAGTAGAGACGGGGGTTTCTCCATGTTG AGGCATGCGCCACCATGCCCGGCTAATTTTGTGTTTTTAGTAGAGACGGGGGTTTCTCCATGTTG T C SFXN4 Ensembl:ENSG00000183605 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1036578014 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13049,RMVar_hsa_circ_83195,RMVar_hsa_circ_49112,RMVar_hsa_circ_269372,RMVar_hsa_circ_146661 30219 RMVar_ID_30219 Human_SNP_ID_448991625 A-to-I Human chr10 - 119163892 119163892 119163892 GGGATTGCAGGCATGCGCCACCATGCCCGGCTAATTTTGTATTTTTAGTAGAGACGGGGGTTTCT GGGATTGCAGGCATGCGCCACCATGCCCGGCTGATTTTGTATTTTTAGTAGAGACGGGGGTTTCT T C SFXN4 Ensembl:ENSG00000183605 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1239812873 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13049,RMVar_hsa_circ_83195,RMVar_hsa_circ_49112,RMVar_hsa_circ_269372,RMVar_hsa_circ_146661 30220 RMVar_ID_30220 Human_SNP_ID_448993571 A-to-I Human chr10 - 119170638 119170638 119170638 GCCTGCCTCGGCCTCTCAAAAGTGCTGGGATTACAGGCATGAGCCACCGCACCTGGCAGACCATT GCCTGCCTCGGCCTCTCAAAAGTGCTGGGATTCCAGGCATGAGCCACCGCACCTGGCAGACCATT T G PRDX3 Ensembl:ENSG00000165672 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1248302755 Functional Loss SNV dbSNP153 33..33 33 - - - 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 30221 RMVar_ID_30221 Human_SNP_ID_448995573 A-to-I Human chr10 - 119177597 119177597 119177597 GTTAGAGTGCAATGGCGCGATCTCGGCTCTGCAACCTCTGCCTCCCGGGTTCAAGCAATTCTCCT GTTAGAGTGCAATGGCGCGATCTCGGCTCTGCGACCTCTGCCTCCCGGGTTCAAGCAATTCTCCT T C PRDX3 Ensembl:ENSG00000165672 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1228648213 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77866,RMVar_hsa_circ_146665 30222 RMVar_ID_30222 Human_SNP_ID_449078018 A-to-I Human chr10 - 119503826 119503826 119503826 GACATTGAGGTGAGCTCTAACCCAATCTGACTAGTGTCCTTGTGAGAAGAGGAGGTAAGGACACA GACATTGAGGTGAGCTCTAACCCAATCTGACTGGTGTCCTTGTGAGAAGAGGAGGTAAGGACACA T C RGS10 Ensembl:ENSG00000148908 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1471147318 Functional Loss SNV dbSNP153 33..33 33 - - - 30223 RMVar_ID_30223 Human_SNP_ID_449079696 A-to-I Human chr10 - 119510857 119510857 119510857 AAAATTAGCCAAGTGTGGTGGTGGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTAGCCAAGTGTGGTGGTGGGCGCCTGTCGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA T G RGS10 Ensembl:ENSG00000148908 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs181859750 Functional Loss SNV dbSNP153 33..33 33 - - - 30224 RMVar_ID_30224 Human_SNP_ID_449094902 A-to-I Human chr10 - 119570967 119570967 119570967 TGGAGTTTGCAGTGTGCTGAGATTGTGTCACTACAATCCAGCCTGGGCAGCAGAGCAAGACTCTG TGGAGTTTGCAGTGTGCTGAGATTGTGTCACTGCAATCCAGCCTGGGCAGCAGAGCAAGACTCTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs983576814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24786992 30225 RMVar_ID_30225 Human_SNP_ID_449095114 A-to-I Human chr10 + 119572016 119572016 119572016 CAGAAACACATCACCAAAATAAATCTCAAAATAATTATGAAATAAAAAACATTTCCTTGCATGCC CAGAAACACATCACCAAAATAAATCTCAAAATGATTATGAAATAAAAAACATTTCCTTGCATGCC A G lnc-BAG3-1,lnc-BAG3-1:2 RNACentral:URS00009C4D24,RNACentral:URS00008BA217 lincRNA,lincRNA exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs371200191 Functional Loss SNV dbSNP153 33..33 33 - - - 30226 RMVar_ID_30226 Human_SNP_ID_449095189 A-to-I Human chr10 - 119572252 119572252 119572252 CAGGAGAATTGAACCTGGGAGGTGGAGGTTGCAGTGAGCTGAAAATGCGCCACTGCACTCCAGCC CAGGAGAATTGAACCTGGGAGGTGGAGGTTGCGGTGAGCTGAAAATGCGCCACTGCACTCCAGCC T C TIAL1 Ensembl:ENSG00000151923 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs946545861 Functional Loss SNV dbSNP153 33..33 33 - - - 30227 RMVar_ID_30227 Human_SNP_ID_449095199 A-to-I Human chr10 - 119572310 119572310 119572310 AAAATTAGCTGGGCGTGCTGGTGGGCGCTGGTAGTCCCAGTGACTTGGGAGGCTGAGGCAGGAGA AAAATTAGCTGGGCGTGCTGGTGGGCGCTGGTGGTCCCAGTGACTTGGGAGGCTGAGGCAGGAGA T C TIAL1 Ensembl:ENSG00000151923 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1374988473 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26393181 30228 RMVar_ID_30228 Human_SNP_ID_449095230 A-to-I Human chr10 - 119572442 119572442 119572442 CGGGCATGGTGGTTCACACCTGTAATCCCAGCACTTTGGGAAGCTGAGGCGGGTAGTGGATCACC CGGGCATGGTGGTTCACACCTGTAATCCCAGCCCTTTGGGAAGCTGAGGCGGGTAGTGGATCACC T G TIAL1 Ensembl:ENSG00000151923 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1346328523 Functional Loss SNV dbSNP153 33..33 33 - - - 30229 RMVar_ID_30229 Human_SNP_ID_449095264 A-to-I Human chr10 - 119572512 119572512 119572512 TGCTATTGCACTCCACCCTGGGAAATAGAGCAAGACTCCGTCTCAAAAAAAAAAAAAGTGCAACT TGCTATTGCACTCCACCCTGGGAAATAGAGCAGGACTCCGTCTCAAAAAAAAAAAAAGTGCAACT T C TIAL1 Ensembl:ENSG00000151923 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs970282012 Functional Loss SNV dbSNP153 33..33 33 - - - 30230 RMVar_ID_30230 Human_SNP_ID_449095273 A-to-I Human chr10 - 119572550 119572550 119572550 TGAACCCAGGAGGCGGAGGTTGCCCTGAGCCAAGATTGTGCTATTGCACTCCACCCTGGGAAATA TGAACCCAGGAGGCGGAGGTTGCCCTGAGCCAGGATTGTGCTATTGCACTCCACCCTGGGAAATA T C TIAL1 Ensembl:ENSG00000151923 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1453290828 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22787630 30231 RMVar_ID_30231 Human_SNP_ID_449095287 A-to-I Human chr10 - 119572614 119572614 119572614 ATTAAGCGTGGTGGCCCGTGCCTGTAGTCTCAACTACTCAGGAGGCTGAGGCAGGAGAATCTCTT ATTAAGCGTGGTGGCCCGTGCCTGTAGTCTCAGCTACTCAGGAGGCTGAGGCAGGAGAATCTCTT T C TIAL1 Ensembl:ENSG00000151923 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1463182240 Functional Loss SNV dbSNP153 33..33 33 - - - 30232 RMVar_ID_30232 Human_SNP_ID_449095307 A-to-I Human chr10 - 119572679 119572679 119572679 TGGGCCGGGCGCAGTGGCTCAGCCTGACCAACATGATGAAACCCTGTCTCCACTAAAAATACAAA TGGGCCGGGCGCAGTGGCTCAGCCTGACCAACGTGATGAAACCCTGTCTCCACTAAAAATACAAA T C TIAL1 Ensembl:ENSG00000151923 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs534555297 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_371940 30233 RMVar_ID_30233 Human_SNP_ID_449095370 A-to-I Human chr10 - 119572947 119572947 119572947 GGTTCAAGCTATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGACTACAGATGCATGCCACCATGTC GGTTCAAGCTATTCTCCTGCCTCAGCCTCCCGTGTAGCTGGACTACAGATGCATGCCACCATGTC T A TIAL1 Ensembl:ENSG00000151923 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1297713358 Functional Loss SNV dbSNP153 33..33 33 - - - 30234 RMVar_ID_30234 Human_SNP_ID_449095445 A-to-I Human chr10 - 119573096 119573096 119573096 CCGCCTCAGTCTCCCAAAGTGCTGGGACTACAAGCGTGAGCCACGGTGTCTGGCTTTTTTTTTTT CCGCCTCAGTCTCCCAAAGTGCTGGGACTACATGCGTGAGCCACGGTGTCTGGCTTTTTTTTTTT T A TIAL1 Ensembl:ENSG00000151923 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1307002967 Functional Loss SNV dbSNP153 33..33 33 - - - 30235 RMVar_ID_30235 Human_SNP_ID_449095446 A-to-I Human chr10 - 119573096 119573096 119573096 CCGCCTCAGTCTCCCAAAGTGCTGGGACTACAAGCGTGAGCCACGGTGTCTGGCTTTTTTTTTTT CCGCCTCAGTCTCCCAAAGTGCTGGGACTACAGGCGTGAGCCACGGTGTCTGGCTTTTTTTTTTT T C TIAL1 Ensembl:ENSG00000151923 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1307002967 Functional Loss SNV dbSNP153 33..33 33 - - - 30236 RMVar_ID_30236 Human_SNP_ID_449095509 A-to-I Human chr10 - 119573279 119573279 119573279 GAACTTGGCTCACCGCAACCTCTGCTTCCCAGATTCAAGCGATTCTCCTGCCTCAGCCTCCTGAG GAACTTGGCTCACCGCAACCTCTGCTTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGAG T C TIAL1 Ensembl:ENSG00000151923 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1448262584 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11280497,Human_RBP_ID_26393183 30237 RMVar_ID_30237 Human_SNP_ID_449099900 A-to-I Human chr10 - 119591338 119591338 119591338 CCATGGCGCGATCTCAGCCCACTGCAACCTCCACCTCCCGGGTTCAAGTGATTCTCCTGCCTCAG CCATGGCGCGATCTCAGCCCACTGCAACCTCCGCCTCCCGGGTTCAAGTGATTCTCCTGCCTCAG T C TIAL1 Ensembl:ENSG00000151923 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs936171605 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21522,RMVar_hsa_circ_103966,RMVar_hsa_circ_36528,RMVar_hsa_circ_146685,RMVar_hsa_circ_56726,RMVar_hsa_circ_146689,RMVar_hsa_circ_315968 30238 RMVar_ID_30238 Human_SNP_ID_449167986 A-to-I Human chr10 - 119850585 119850585 119850585 ATCACCACGCCTGGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGA ATCACCACGCCTGGCTAATTTTTTGTATTTTTTGTAGAGACGGGGTTTCACCGTGTTAGCCAGGA T A MCMBP Ensembl:ENSG00000197771 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1564879267 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_363649,RMVar_hsa_circ_36202,RMVar_hsa_circ_313876,RMVar_hsa_circ_16674,RMVar_hsa_circ_11496,RMVar_hsa_circ_146712,RMVar_hsa_circ_61897,RMVar_hsa_circ_50459,RMVar_hsa_circ_265043,RMVar_hsa_circ_318578,RMVar_hsa_circ_295311,RMVar_hsa_circ_146718,RMVar_hsa_circ_368704,RMVar_hsa_circ_146719 30239 RMVar_ID_30239 Human_SNP_ID_449167987 A-to-I Human chr10 - 119850591 119850591 119850591 GCCCCCATCACCACGCCTGGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCGTGTTAG GCCCCCATCACCACGCCTGGCTAATTTTTTGTGTTTTTAGTAGAGACGGGGTTTCACCGTGTTAG T C MCMBP Ensembl:ENSG00000197771 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1349869392 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_363649,RMVar_hsa_circ_36202,RMVar_hsa_circ_313876,RMVar_hsa_circ_16674,RMVar_hsa_circ_11496,RMVar_hsa_circ_146712,RMVar_hsa_circ_61897,RMVar_hsa_circ_50459,RMVar_hsa_circ_265043,RMVar_hsa_circ_318578,RMVar_hsa_circ_295311,RMVar_hsa_circ_146718,RMVar_hsa_circ_368704,RMVar_hsa_circ_146719 30240 RMVar_ID_30240 Human_SNP_ID_449168274 A-to-I Human chr10 - 119851549 119851549 119851549 AGGCGCCTGTAATCCCAGCTGTTTGGGAGGCTAAGGCAGTAGAATCACTTGAACCCAGAGGGGCG AGGCGCCTGTAATCCCAGCTGTTTGGGAGGCTGAGGCAGTAGAATCACTTGAACCCAGAGGGGCG T C MCMBP Ensembl:ENSG00000197771 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1183562056 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_363649,RMVar_hsa_circ_36202,RMVar_hsa_circ_313876,RMVar_hsa_circ_16674,RMVar_hsa_circ_11496,RMVar_hsa_circ_146712,RMVar_hsa_circ_61897,RMVar_hsa_circ_50459,RMVar_hsa_circ_265043,RMVar_hsa_circ_318578,RMVar_hsa_circ_295311,RMVar_hsa_circ_146718,RMVar_hsa_circ_368704,RMVar_hsa_circ_146719 30241 RMVar_ID_30241 Human_SNP_ID_449169748 A-to-I Human chr10 - 119857031 119857031 119857031 CAGTGGCACAAACATGGCTCATTGCTGCTTCAACCTCCTGGGCTCAAGCAGTCCTCTTGCCTCAG CAGTGGCACAAACATGGCTCATTGCTGCTTCACCCTCCTGGGCTCAAGCAGTCCTCTTGCCTCAG T G MCMBP Ensembl:ENSG00000197771 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935033113 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36202,RMVar_hsa_circ_16674,RMVar_hsa_circ_11496,RMVar_hsa_circ_146712,RMVar_hsa_circ_61897,RMVar_hsa_circ_50459,RMVar_hsa_circ_265043,RMVar_hsa_circ_295311,RMVar_hsa_circ_146718,RMVar_hsa_circ_368704,RMVar_hsa_circ_108459,RMVar_hsa_circ_329119,RMVar_hsa_circ_146719,RMVar_hsa_circ_272237,RMVar_hsa_circ_146721,RMVar_hsa_circ_146722,RMVar_hsa_circ_146720 30242 RMVar_ID_30242 Human_SNP_ID_449184032 A-to-I Human chr10 + 119911499 119911499 119911499 GCTTTTATTTTTGTTTAGTTTTTTTTTGAGACAGGATTTTGCTCTGTTGCCCAGGCTGAAGTGCA GCTTTTATTTTTGTTTAGTTTTTTTTTGAGACGGGATTTTGCTCTGTTGCCCAGGCTGAAGTGCA A G SEC23IP Ensembl:ENSG00000107651 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs925502059 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11282835 RMVar_hsa_circ_58539,RMVar_hsa_circ_333640,RMVar_hsa_circ_352817,RMVar_hsa_circ_76406,RMVar_hsa_circ_146727,RMVar_hsa_circ_37546,RMVar_hsa_circ_370874,RMVar_hsa_circ_28285,RMVar_hsa_circ_325492,RMVar_hsa_circ_146730,RMVar_hsa_circ_344935,RMVar_hsa_circ_347354,RMVar_hsa_circ_340413,RMVar_hsa_circ_289301,RMVar_hsa_circ_302391,RMVar_hsa_circ_68338,RMVar_hsa_circ_146732,RMVar_hsa_circ_146733,RMVar_hsa_circ_146731 30243 RMVar_ID_30243 Human_SNP_ID_449184617 A-to-I Human chr10 + 119913701 119913701 119913701 TTTAGTGGAGACAGCGTTTTGCCATGTTGGCCAGGCTGGTTTTGAACTCCTGACATCAAGTGATC TTTAGTGGAGACAGCGTTTTGCCATGTTGGCCCGGCTGGTTTTGAACTCCTGACATCAAGTGATC A C SEC23IP Ensembl:ENSG00000107651 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1473598989 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14746,RMVar_hsa_circ_58539,RMVar_hsa_circ_333640,RMVar_hsa_circ_76406,RMVar_hsa_circ_146727,RMVar_hsa_circ_37546,RMVar_hsa_circ_111449,RMVar_hsa_circ_28285,RMVar_hsa_circ_325492,RMVar_hsa_circ_344935,RMVar_hsa_circ_347354,RMVar_hsa_circ_340413,RMVar_hsa_circ_302391,RMVar_hsa_circ_68338,RMVar_hsa_circ_146732,RMVar_hsa_circ_146733,RMVar_hsa_circ_327018,RMVar_hsa_circ_370509,RMVar_hsa_circ_146731,RMVar_hsa_circ_346965,RMVar_hsa_circ_313261,RMVar_hsa_circ_65002,RMVar_hsa_circ_65616,RMVar_hsa_circ_53138,RMVar_hsa_circ_146734,RMVar_hsa_circ_146736,RMVar_hsa_circ_146737,RMVar_hsa_circ_146738,RMVar_hsa_circ_146735 30244 RMVar_ID_30244 Human_SNP_ID_449184630 A-to-I Human chr10 + 119913753 119913753 119913753 ACATCAAGTGATCCACGTGCCTCGGCCTCCTAAAGTTCTGGAATTACAGGCGTGAGCCACCACAC ACATCAAGTGATCCACGTGCCTCGGCCTCCTACAGTTCTGGAATTACAGGCGTGAGCCACCACAC A C SEC23IP Ensembl:ENSG00000107651 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs200101303 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14746,RMVar_hsa_circ_58539,RMVar_hsa_circ_333640,RMVar_hsa_circ_76406,RMVar_hsa_circ_146727,RMVar_hsa_circ_37546,RMVar_hsa_circ_111449,RMVar_hsa_circ_28285,RMVar_hsa_circ_325492,RMVar_hsa_circ_344935,RMVar_hsa_circ_347354,RMVar_hsa_circ_340413,RMVar_hsa_circ_302391,RMVar_hsa_circ_68338,RMVar_hsa_circ_146732,RMVar_hsa_circ_146733,RMVar_hsa_circ_327018,RMVar_hsa_circ_370509,RMVar_hsa_circ_146731,RMVar_hsa_circ_346965,RMVar_hsa_circ_313261,RMVar_hsa_circ_65002,RMVar_hsa_circ_65616,RMVar_hsa_circ_53138,RMVar_hsa_circ_146734,RMVar_hsa_circ_146736,RMVar_hsa_circ_146737,RMVar_hsa_circ_146738,RMVar_hsa_circ_146735 30245 RMVar_ID_30245 Human_SNP_ID_449190839 A-to-I Human chr10 + 119939048 119939048 119939048 AAGCCTCAAATTGGCCAGGTGTGGTGGCTTACACCTGTAATCTTAGCACTTTGGAGGCTGAGGCA AAGCCTCAAATTGGCCAGGTGTGGTGGCTTACCCCTGTAATCTTAGCACTTTGGAGGCTGAGGCA A C SEC23IP Ensembl:ENSG00000107651 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1435831870 Functional Loss SNV dbSNP153 33..33 33 - - - 30246 RMVar_ID_30246 Human_SNP_ID_449190840 A-to-I Human chr10 + 119939048 119939048 119939048 AAGCCTCAAATTGGCCAGGTGTGGTGGCTTACACCTGTAATCTTAGCACTTTGGAGGCTGAGGCA AAGCCTCAAATTGGCCAGGTGTGGTGGCTTACGCCTGTAATCTTAGCACTTTGGAGGCTGAGGCA A G SEC23IP Ensembl:ENSG00000107651 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1435831870 Functional Loss SNV dbSNP153 33..33 33 - - - 30247 RMVar_ID_30247 Human_SNP_ID_449190935 A-to-I Human chr10 + 119939521 119939521 119939521 AAATAGTGAAATCTTGTCTCTACTAAAAATACAAAAATTAGCCGGGCGTGGTAGCACACACCTGT AAATAGTGAAATCTTGTCTCTACTAAAAATACGAAAATTAGCCGGGCGTGGTAGCACACACCTGT A G SEC23IP Ensembl:ENSG00000107651 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1035751942 Functional Loss SNV dbSNP153 33..33 33 - - - 30248 RMVar_ID_30248 Human_SNP_ID_449191005 A-to-I Human chr10 + 119939808 119939808 119939808 ACCTCTGACTCCCAGGCTCAAGCGATCCTCCTAACTTAGCATCTCGAGAGGCTGGGACCACAGGT ACCTCTGACTCCCAGGCTCAAGCGATCCTCCTGACTTAGCATCTCGAGAGGCTGGGACCACAGGT A G SEC23IP Ensembl:ENSG00000107651 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1367066315 Functional Loss SNV dbSNP153 33..33 33 - - - 30249 RMVar_ID_30249 Human_SNP_ID_449191019 A-to-I Human chr10 + 119939861 119939861 119939861 GGGACCACAGGTGTGCACCACCACGTCTGGCTAATTTTTTTATTTTTTGGTAGAGACAGGGTTCC GGGACCACAGGTGTGCACCACCACGTCTGGCTGATTTTTTTATTTTTTGGTAGAGACAGGGTTCC A G SEC23IP Ensembl:ENSG00000107651 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs889017203 Functional Loss SNV dbSNP153 33..33 33 - - - 30250 RMVar_ID_30250 Human_SNP_ID_449204975 A-to-I Human chr10 - 119997516 119997516 119997516 TAAAGAACCAGTCAGCAAAGCAAAACAGAGTCAGAGTGAAAAGAAAGCACAGAAGGCTATGTCCA TAAAGAACCAGTCAGCAAAGCAAAACAGAGTCGGAGTGAAAAGAAAGCACAGAAGGCTATGTCCA T C NACAP2 Ensembl:ENSG00000180230 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1242239047 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1860178 30251 RMVar_ID_30251 Human_SNP_ID_449204982 A-to-I Human chr10 - 119997547 119997547 119997547 AAGCCCAGCTGGCAGCAGCAGCTGAAATTAATAAAGAACCAGTCAGCAAAGCAAAACAGAGTCAG AAGCCCAGCTGGCAGCAGCAGCTGAAATTAATGAAGAACCAGTCAGCAAAGCAAAACAGAGTCAG T C NACAP2 Ensembl:ENSG00000180230 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1346991152 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1899088 30252 RMVar_ID_30252 Human_SNP_ID_449204983 A-to-I Human chr10 - 119997550 119997550 119997550 AACAAGCCCAGCTGGCAGCAGCAGCTGAAATTAATAAAGAACCAGTCAGCAAAGCAAAACAGAGT AACAAGCCCAGCTGGCAGCAGCAGCTGAAATTGATAAAGAACCAGTCAGCAAAGCAAAACAGAGT T C NACAP2 Ensembl:ENSG00000180230 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1276443903 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17679585,Human_RBP_ID_26875737 Human_miRNA_ID_1899088 30253 RMVar_ID_30253 Human_SNP_ID_449204984 A-to-I Human chr10 - 119997550 119997550 119997550 AACAAGCCCAGCTGGCAGCAGCAGCTGAAATTAATAAAGAACCAGTCAGCAAAGCAAAACAGAGT AACAAGCCCAGCTGGCAGCAGCAGCTGAAATTCATAAAGAACCAGTCAGCAAAGCAAAACAGAGT T G NACAP2 Ensembl:ENSG00000180230 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1276443903 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17679585,Human_RBP_ID_26875737 Human_miRNA_ID_1899088 30254 RMVar_ID_30254 Human_SNP_ID_449204989 A-to-I Human chr10 - 119997566 119997566 119997566 ACACAGACAACCACACAACAAGCCCAGCTGGCAGCAGCAGCTGAAATTAATAAAGAACCAGTCAG ACACAGACAACCACACAACAAGCCCAGCTGGCGGCAGCAGCTGAAATTAATAAAGAACCAGTCAG T C NACAP2 Ensembl:ENSG00000180230 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1338803146 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8245322,Human_RBP_ID_17462329,Human_RBP_ID_17672938,Human_RBP_ID_17679585,Human_RBP_ID_17787612,Human_RBP_ID_18510347,Human_RBP_ID_26875737 30255 RMVar_ID_30255 Human_SNP_ID_449204993 A-to-I Human chr10 - 119997592 119997592 119997592 TACCAGAGTTTGAGGAACAGGATTCCACACAGACAACCACACAACAAGCCCAGCTGGCAGCAGCA TACCAGAGTTTGAGGAACAGGATTCCACACAGGCAACCACACAACAAGCCCAGCTGGCAGCAGCA T C NACAP2 Ensembl:ENSG00000180230 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1359038534 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17672938 Human_miRNA_ID_1829061 30256 RMVar_ID_30256 Human_SNP_ID_721239973 A-to-I Human chrX + 75322298 75322298 75322298 CAGTGGCATGATCAGGCCTCACTGCAGCCGCTATCCCCCATAAAGTGATCATCTCAGCCCCTGGA CAGTGGCATGATCAGGCCTCACTGCAGCCGCTGTCCCCCATAAAGTGATCATCTCAGCCCCTGGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1192954260 Functional Loss SNV dbSNP153 33..33 33 - - - 30257 RMVar_ID_30257 Human_SNP_ID_721302245 A-to-I Human chrX + 75584926 75584926 75584926 GAGATGAGAGACCACTCTTTCCCCAAATTCTCACCTCTATTAAGCTGCTGACCCGCTCATTGCCA GAGATGAGAGACCACTCTTTCCCCAAATTCTCGCCTCTATTAAGCTGCTGACCCGCTCATTGCCA A G BRAFP1 Ensembl:ENSG00000224775 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1193016683 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9250530 RMVar_hsa_circ_263073 30258 RMVar_ID_30258 Human_SNP_ID_721302249 A-to-I Human chrX + 75584944 75584944 75584944 TTCCCCAAATTCTCACCTCTATTAAGCTGCTGACCCGCTCATTGCCAAAAATTCACCACAGTGCA TTCCCCAAATTCTCACCTCTATTAAGCTGCTGCCCCGCTCATTGCCAAAAATTCACCACAGTGCA A C BRAFP1 Ensembl:ENSG00000224775 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1446665436 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_263073 30259 RMVar_ID_30259 Human_SNP_ID_721346140 A-to-I Human chrX + 75741689 75741689 75741689 TCATCATGGCCTGAAGACTCAGGGAGTAACTCAGGATGAACCGTGTTACAGGCAGGAAATGAAAG TCATCATGGCCTGAAGACTCAGGGAGTAACTCGGGATGAACCGTGTTACAGGCAGGAAATGAAAG A G lnc-UPRT-6,lnc-UPRT-6:2 RNACentral:URS0000D5A8D3,RNACentral:URS0000D59F2E lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs761200900 Functional Loss SNV dbSNP153 33..33 33 - - - 30260 RMVar_ID_30260 Human_SNP_ID_721346141 A-to-I Human chrX + 75741689 75741689 75741689 TCATCATGGCCTGAAGACTCAGGGAGTAACTCAGGATGAACCGTGTTACAGGCAGGAAATGAAAG TCATCATGGCCTGAAGACTCAGGGAGTAACTCTGGATGAACCGTGTTACAGGCAGGAAATGAAAG A T lnc-UPRT-6,lnc-UPRT-6:2 RNACentral:URS0000D5A8D3,RNACentral:URS0000D59F2E lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs761200900 Functional Loss SNV dbSNP153 33..33 33 - - - 30261 RMVar_ID_30261 Human_SNP_ID_721346287 A-to-I Human chrX - 75742164 75742164 75742164 GAAGAAGAAAATTAAAAAGGTTTCAAATGCCAATGAAATGTATACCCAGAAAAATGATGGAAACG GAAGAAGAAAATTAAAAAGGTTTCAAATGCCAGTGAAATGTATACCCAGAAAAATGATGGAAACG T C TTC3P1 Ensembl:ENSG00000215105 Pseudogene exon GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1431683166 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3932049 30262 RMVar_ID_30262 Human_SNP_ID_721346386 A-to-I Human chrX - 75742452 75742452 75742452 CAATACTGAGCCATATAATCCTTTTGAGAAACAACAAGGGGAAATTTCACGGATTGAAAAGGAGT CAATACTGAGCCATATAATCCTTTTGAGAAACGACAAGGGGAAATTTCACGGATTGAAAAGGAGT T C TTC3P1 Ensembl:ENSG00000215105 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878937285 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3932049 30263 RMVar_ID_30263 Human_SNP_ID_721346387 A-to-I Human chrX - 75742452 75742452 75742452 CAATACTGAGCCATATAATCCTTTTGAGAAACAACAAGGGGAAATTTCACGGATTGAAAAGGAGT CAATACTGAGCCATATAATCCTTTTGAGAAACCACAAGGGGAAATTTCACGGATTGAAAAGGAGT T G TTC3P1 Ensembl:ENSG00000215105 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878937285 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3932049 30264 RMVar_ID_30264 Human_SNP_ID_721346388 A-to-I Human chrX - 75742456 75742456 75742456 AAGTCAATACTGAGCCATATAATCCTTTTGAGAAACAACAAGGGGAAATTTCACGGATTGAAAAG AAGTCAATACTGAGCCATATAATCCTTTTGAGGAACAACAAGGGGAAATTTCACGGATTGAAAAG T C TTC3P1 Ensembl:ENSG00000215105 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879057871 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3932049 30265 RMVar_ID_30265 Human_SNP_ID_721346980 A-to-I Human chrX - 75745678 75745678 75745678 TGGCTAACGGTGGTAATCAGAATCTAAAGGTGATGGATGAGGCATTGATGGTAGATGATTGTGAC TGGCTAACGGTGGTAATCAGAATCTAAAGGTGGTGGATGAGGCATTGATGGTAGATGATTGTGAC T C TTC3P1 Ensembl:ENSG00000215105 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1234789240 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5108111,Human_RBP_ID_8031061,Human_RBP_ID_22413411 Human_miRNA_ID_1907972 30266 RMVar_ID_30266 Human_SNP_ID_721347050 A-to-I Human chrX + 75746060 75746060 75746060 TTCTTCAGAATAGTGGCTCTCTTTCCATCACCAAGTGCATTTCTAAACTGTCCAGTACGAAGAAA TTCTTCAGAATAGTGGCTCTCTTTCCATCACCCAGTGCATTTCTAAACTGTCCAGTACGAAGAAA A C lnc-UPRT-6,lnc-UPRT-6:2 RNACentral:URS0000D5A8D3,RNACentral:URS0000D59F2E lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1380520951 Functional Loss SNV dbSNP153 33..33 33 - - - 30267 RMVar_ID_30267 Human_SNP_ID_721850328 A-to-I Human chrX - 77577363 77577363 77577363 AGAAGCACATGAAAAGATGTCTAGCATCACTAATCCTTAGGGAAATGCAAATGAAAACTGTAATG AGAAGCACATGAAAAGATGTCTAGCATCACTAGTCCTTAGGGAAATGCAAATGAAAACTGTAATG T C ATRX Ensembl:ENSG00000085224 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1386578952 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_402,RMVar_hsa_circ_35305,RMVar_hsa_circ_439,RMVar_hsa_circ_303420,RMVar_hsa_circ_346471,RMVar_hsa_circ_352342,RMVar_hsa_circ_333427,RMVar_hsa_circ_288217,RMVar_hsa_circ_282550,RMVar_hsa_circ_74189,RMVar_hsa_circ_271156,RMVar_hsa_circ_15345,RMVar_hsa_circ_26967,RMVar_hsa_circ_325708,RMVar_hsa_circ_23074,RMVar_hsa_circ_351221,RMVar_hsa_circ_353228,RMVar_hsa_circ_340208,RMVar_hsa_circ_307737,RMVar_hsa_circ_320836,RMVar_hsa_circ_47858 30268 RMVar_ID_30268 Human_SNP_ID_721872247 A-to-I Human chrX - 77705691 77705691 77705691 TTGTTTTTTCTTGGTAGAGATGAGGTTTCACTATGTTTCTGAGGCTGTTCTTAAACTTCTGTCCT TTGTTTTTTCTTGGTAGAGATGAGGTTTCACTGTGTTTCTGAGGCTGTTCTTAAACTTCTGTCCT T C ATRX Ensembl:ENSG00000085224 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924275319 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26297221 RMVar_hsa_circ_12638,RMVar_hsa_circ_66963,RMVar_hsa_circ_296028,RMVar_hsa_circ_44895 30269 RMVar_ID_30269 Human_SNP_ID_721881926 A-to-I Human chrX - 77757916 77757916 77757916 GTTTAAAGATAAGTCAATTGGGAGGCCGAGGCAGGTGAATCACGAGGTCAGGAGTTCAAGACCAG GTTTAAAGATAAGTCAATTGGGAGGCCGAGGCCGGTGAATCACGAGGTCAGGAGTTCAAGACCAG T G ATRX Ensembl:ENSG00000085224 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs782714398 Functional Loss SNV dbSNP153 33..33 33 - - - 30270 RMVar_ID_30270 Human_SNP_ID_721882525 A-to-I Human chrX - 77761415 77761415 77761415 ATCCCACCTCAGCCCCCCAAGTAGCTGGGACTACAGGTGTATGCTACCATGCCTGGCTAATTTTT ATCCCACCTCAGCCCCCCAAGTAGCTGGGACTCCAGGTGTATGCTACCATGCCTGGCTAATTTTT T G ATRX Ensembl:ENSG00000085224 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1289932543 Functional Loss SNV dbSNP153 33..33 33 - - - 30271 RMVar_ID_30271 Human_SNP_ID_721883210 A-to-I Human chrX - 77764984 77764984 77764984 TTTTGTAGAGGCAGGGTTTCACCATGTCGGCGAGGCTGGTCTTGAACTCTTGACCTCATGTGATC TTTTGTAGAGGCAGGGTTTCACCATGTCGGCGCGGCTGGTCTTGAACTCTTGACCTCATGTGATC T G ATRX Ensembl:ENSG00000085224 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1557194682 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16944977 30272 RMVar_ID_30272 Human_SNP_ID_721883236 A-to-I Human chrX - 77765045 77765045 77765045 CTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCACCCACCACCACACCTGACTAATTTTT CTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTGCAGGCACCCACCACCACACCTGACTAATTTTT T C ATRX Ensembl:ENSG00000085224 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1430150760 Functional Loss SNV dbSNP153 33..33 33 - - - 30273 RMVar_ID_30273 Human_SNP_ID_721884909 A-to-I Human chrX - 77772940 77772940 77772940 GGGAGGCTGAGGAGGGAGGATCCTTTGAGCACAGGAGTCTGAGGCTGCAGTGAGCTATGATTATA GGGAGGCTGAGGAGGGAGGATCCTTTGAGCACCGGAGTCTGAGGCTGCAGTGAGCTATGATTATA T G ATRX Ensembl:ENSG00000085224 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1557200058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16945154 30274 RMVar_ID_30274 Human_SNP_ID_721886540 A-to-I Human chrX - 77780829 77780829 77780829 TCAAGCAATCCTCCTGCTTCAGCCTCCCATGTAGCTGGGACCACAGGTGTGTCATCATGCCCCGC TCAAGCAATCCTCCTGCTTCAGCCTCCCATGTGGCTGGGACCACAGGTGTGTCATCATGCCCCGC T C ATRX Ensembl:ENSG00000085224 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs894595996 Functional Loss SNV dbSNP153 33..33 33 - - - 30275 RMVar_ID_30275 Human_SNP_ID_721886550 A-to-I Human chrX - 77780858 77780858 77780858 ATGGCTCACTGTAGCCTTGACCTCCTGGCTCAAGCAATCCTCCTGCTTCAGCCTCCCATGTAGCT ATGGCTCACTGTAGCCTTGACCTCCTGGCTCAGGCAATCCTCCTGCTTCAGCCTCCCATGTAGCT T C ATRX Ensembl:ENSG00000085224 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1294410629 Functional Loss SNV dbSNP153 33..33 33 - - - 30276 RMVar_ID_30276 Human_SNP_ID_721886562 A-to-I Human chrX - 77780932 77780932 77780932 ATGGTCTGTAGCATTAATTTTTTTTTGGGACAAGGTCTCACTGTCACCCAAGCTGTAGTGCAGTG ATGGTCTGTAGCATTAATTTTTTTTTGGGACAGGGTCTCACTGTCACCCAAGCTGTAGTGCAGTG T C ATRX Ensembl:ENSG00000085224 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1372936370 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_848314,Human_RBP_ID_16945459,Human_RBP_ID_24354573 30277 RMVar_ID_30277 Human_SNP_ID_721886563 A-to-I Human chrX - 77780933 77780933 77780933 GATGGTCTGTAGCATTAATTTTTTTTTGGGACAAGGTCTCACTGTCACCCAAGCTGTAGTGCAGT GATGGTCTGTAGCATTAATTTTTTTTTGGGACGAGGTCTCACTGTCACCCAAGCTGTAGTGCAGT T C ATRX Ensembl:ENSG00000085224 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs782385659 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_848314,Human_RBP_ID_16945459,Human_RBP_ID_24354573 30278 RMVar_ID_30278 Human_SNP_ID_721894796 A-to-I Human chrX - 77824939 77824939 77824939 GTATTTTTAGTAGAGACGGTTTCACCATGTTGACAAGCCTGGTCTCAAACTCCTGACCTCGGGTG GTATTTTTAGTAGAGACGGTTTCACCATGTTGGCAAGCCTGGTCTCAAACTCCTGACCTCGGGTG T C RF00017-1190,RF00017-4674 RNACentral:URS000092EF5C,RNACentral:URS000094E2D9 SRP RNA,SRP RNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1260958492 Functional Loss SNV dbSNP153 33..33 33 - - - 30279 RMVar_ID_30279 Human_SNP_ID_721895225 A-to-I Human chrX - 77827534 77827534 77827534 AGGAGGCTGAGGCACGAGAATCACTTGAACTCAGGAGATGGAGGTTTCAGTGAGCCAAGATCACA AGGAGGCTGAGGCACGAGAATCACTTGAACTCCGGAGATGGAGGTTTCAGTGAGCCAAGATCACA T G MAGT1 Ensembl:ENSG00000102158 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs782060765 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8227066 RMVar_hsa_circ_91900,RMVar_hsa_circ_124274,RMVar_hsa_circ_117232,RMVar_hsa_circ_263096,RMVar_hsa_circ_263098,RMVar_hsa_circ_81524,RMVar_hsa_circ_263097,RMVar_hsa_circ_263095 30280 RMVar_ID_30280 Human_SNP_ID_721895228 A-to-I Human chrX - 77827574 77827574 77827574 AGCTGGGTGTGGTGGCAGGAGCCTGTAATCCCAGCTACACAGGAGGCTGAGGCACGAGAATCACT AGCTGGGTGTGGTGGCAGGAGCCTGTAATCCCGGCTACACAGGAGGCTGAGGCACGAGAATCACT T C MAGT1 Ensembl:ENSG00000102158 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs567193995 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8227067 RMVar_hsa_circ_91900,RMVar_hsa_circ_124274,RMVar_hsa_circ_117232,RMVar_hsa_circ_263096,RMVar_hsa_circ_263098,RMVar_hsa_circ_81524,RMVar_hsa_circ_263097,RMVar_hsa_circ_263095 30281 RMVar_ID_30281 Human_SNP_ID_721895229 A-to-I Human chrX - 77827579 77827579 77827579 AAATTAGCTGGGTGTGGTGGCAGGAGCCTGTAATCCCAGCTACACAGGAGGCTGAGGCACGAGAA AAATTAGCTGGGTGTGGTGGCAGGAGCCTGTAGTCCCAGCTACACAGGAGGCTGAGGCACGAGAA T C MAGT1 Ensembl:ENSG00000102158 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1557213053 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8227067 RMVar_hsa_circ_91900,RMVar_hsa_circ_124274,RMVar_hsa_circ_117232,RMVar_hsa_circ_263096,RMVar_hsa_circ_263098,RMVar_hsa_circ_81524,RMVar_hsa_circ_263097,RMVar_hsa_circ_263095 30282 RMVar_ID_30282 Human_SNP_ID_721895236 A-to-I Human chrX - 77827621 77827621 77827621 CCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATATAAAAATTAGCTGGGTGTGGTGGCAG CCTGGCCAACATGGTGAAACCCCGTCTCTACTGAAAATATAAAAATTAGCTGGGTGTGGTGGCAG T C MAGT1 Ensembl:ENSG00000102158 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1008065670 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91900,RMVar_hsa_circ_124274,RMVar_hsa_circ_117232,RMVar_hsa_circ_263096,RMVar_hsa_circ_263098,RMVar_hsa_circ_81524,RMVar_hsa_circ_263097,RMVar_hsa_circ_263095 30283 RMVar_ID_30283 Human_SNP_ID_721895254 A-to-I Human chrX - 77827713 77827713 77827713 CTCCCTGGCCAGGCGCAGTGACTTACGCCTGTAATCTCAGCACTTTGGGAGGCCAAGGCAGGCAG CTCCCTGGCCAGGCGCAGTGACTTACGCCTGTGATCTCAGCACTTTGGGAGGCCAAGGCAGGCAG T C MAGT1 Ensembl:ENSG00000102158 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs782749842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_739714,Human_RBP_ID_8226786,Human_RBP_ID_18155029 Human_miRNA_ID_1943817,Human_miRNA_ID_1946853,Human_miRNA_ID_2087460,Human_miRNA_ID_2118008,Human_miRNA_ID_2201592,Human_miRNA_ID_2204657,Human_miRNA_ID_2317188,Human_miRNA_ID_2320343,Human_miRNA_ID_2323497,Human_miRNA_ID_2326673,Human_miRNA_ID_2329759,Human_miRNA_ID_2521050,Human_miRNA_ID_2524218,Human_miRNA_ID_2776073,Human_miRNA_ID_2817102,Human_miRNA_ID_2823398,Human_miRNA_ID_2829529,Human_miRNA_ID_2832686,Human_miRNA_ID_2836813,Human_miRNA_ID_2842161,Human_miRNA_ID_2847222,Human_miRNA_ID_2850249,Human_miRNA_ID_2864367,Human_miRNA_ID_3114104 RMVar_hsa_circ_91900,RMVar_hsa_circ_124274,RMVar_hsa_circ_117232,RMVar_hsa_circ_263096,RMVar_hsa_circ_263098,RMVar_hsa_circ_81524,RMVar_hsa_circ_263097,RMVar_hsa_circ_263095 30284 RMVar_ID_30284 Human_SNP_ID_721895314 A-to-I Human chrX - 77828120 77828120 77828120 TGAAAATTAGCTGGGCTTGGTGGCTCATGCCTATAATCCTAGCTACTTGGGAGGCTGAGGCACGA TGAAAATTAGCTGGGCTTGGTGGCTCATGCCTGTAATCCTAGCTACTTGGGAGGCTGAGGCACGA T C MAGT1 Ensembl:ENSG00000102158 Protein coding 3'UTR GSE47997;GSE100210;GSE99789;GSE112787;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;293 Flip-In T-REx cells,empty vector;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,29129909,29796672,29967493,32596459,32596459 RNA-Seq:(High) rs1206292765 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23204794,Human_RBP_ID_26308902,Human_RBP_ID_26573335 RMVar_hsa_circ_91900,RMVar_hsa_circ_124274,RMVar_hsa_circ_117232,RMVar_hsa_circ_263096,RMVar_hsa_circ_263098,RMVar_hsa_circ_81524,RMVar_hsa_circ_263097,RMVar_hsa_circ_263095 30285 RMVar_ID_30285 Human_SNP_ID_721895322 A-to-I Human chrX - 77828176 77828176 77828176 CAGGAGTTAGAGACCAGCCTGGCCAACAAGGCAAAACCCCGTCTCTACTAAAAATATGAAAATTA CAGGAGTTAGAGACCAGCCTGGCCAACAAGGCGAAACCCCGTCTCTACTAAAAATATGAAAATTA T C MAGT1 Ensembl:ENSG00000102158 Protein coding 3'UTR GSE112787;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 293 Flip-In T-REx cells,empty vector;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29967493,32596459,32596459 RNA-Seq:(High) rs1557213095 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91900,RMVar_hsa_circ_124274,RMVar_hsa_circ_117232,RMVar_hsa_circ_263096,RMVar_hsa_circ_263098,RMVar_hsa_circ_81524,RMVar_hsa_circ_263097,RMVar_hsa_circ_263095 30286 RMVar_ID_30286 Human_SNP_ID_721895368 A-to-I Human chrX - 77828485 77828485 77828485 TCGGCTGACTGCAAACTCTGCCTCCCAGGTTTAAGCGATTCTCCTGTCACAGCTTCCCAAGTAGC TCGGCTGACTGCAAACTCTGCCTCCCAGGTTTGAGCGATTCTCCTGTCACAGCTTCCCAAGTAGC T C MAGT1 Ensembl:ENSG00000102158 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1022610000 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5074300,Human_RBP_ID_26573858 RMVar_hsa_circ_91900,RMVar_hsa_circ_124274,RMVar_hsa_circ_117232,RMVar_hsa_circ_263096,RMVar_hsa_circ_263098,RMVar_hsa_circ_81524,RMVar_hsa_circ_263097,RMVar_hsa_circ_263095 30287 RMVar_ID_30287 Human_SNP_ID_721895369 A-to-I Human chrX - 77828491 77828491 77828491 GTGAGCTCGGCTGACTGCAAACTCTGCCTCCCAGGTTTAAGCGATTCTCCTGTCACAGCTTCCCA GTGAGCTCGGCTGACTGCAAACTCTGCCTCCCCGGTTTAAGCGATTCTCCTGTCACAGCTTCCCA T G MAGT1 Ensembl:ENSG00000102158 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1557213120 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_739725,Human_RBP_ID_26573858 RMVar_hsa_circ_91900,RMVar_hsa_circ_124274,RMVar_hsa_circ_117232,RMVar_hsa_circ_263096,RMVar_hsa_circ_263098,RMVar_hsa_circ_81524,RMVar_hsa_circ_263097,RMVar_hsa_circ_263095 30288 RMVar_ID_30288 Human_SNP_ID_721895384 A-to-I Human chrX - 77828563 77828563 77828563 TCTATGATTGTTTTTGTTTTGTTGTTTTTTTGAGACGGTCTCGCTGTGTCACACAGGCTGGAGTG TCTATGATTGTTTTTGTTTTGTTGTTTTTTTGTGACGGTCTCGCTGTGTCACACAGGCTGGAGTG T A MAGT1 Ensembl:ENSG00000102158 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs952944092 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_93539,Human_RBP_ID_3929333,Human_RBP_ID_8026607,Human_RBP_ID_18155035,Human_RBP_ID_23204801,Human_RBP_ID_24354642,Human_RBP_ID_24528363,Human_RBP_ID_26573859 Human_miRNA_ID_1104047,Human_miRNA_ID_1530958 RMVar_hsa_circ_91900,RMVar_hsa_circ_124274,RMVar_hsa_circ_117232,RMVar_hsa_circ_263096,RMVar_hsa_circ_263098,RMVar_hsa_circ_81524,RMVar_hsa_circ_263097,RMVar_hsa_circ_263095 30289 RMVar_ID_30289 Human_SNP_ID_721898033 A-to-I Human chrX - 77842375 77842375 77842375 GGAGAATTTTTTTTTTGACACAGTCTAGTTCTATCATGCAGGCTAGAGTGCAGTGGTATGATCAC GGAGAATTTTTTTTTTGACACAGTCTAGTTCTGTCATGCAGGCTAGAGTGCAGTGGTATGATCAC T C MAGT1 Ensembl:ENSG00000102158 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1369268582 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17563,RMVar_hsa_circ_91900,RMVar_hsa_circ_117232,RMVar_hsa_circ_68499,RMVar_hsa_circ_263096,RMVar_hsa_circ_81524,RMVar_hsa_circ_263097,RMVar_hsa_circ_263095,RMVar_hsa_circ_313947,RMVar_hsa_circ_83099,RMVar_hsa_circ_355299,RMVar_hsa_circ_312937,RMVar_hsa_circ_37470,RMVar_hsa_circ_263101,RMVar_hsa_circ_263102 30290 RMVar_ID_30290 Human_SNP_ID_721899281 A-to-I Human chrX - 77848413 77848413 77848413 CCAGGCTGGTCTCGAACTCCTGACCTTAGGTGATCCACCCGTCTTGGCCACAAGCGTGAGCCACC CCAGGCTGGTCTCGAACTCCTGACCTTAGGTGTTCCACCCGTCTTGGCCACAAGCGTGAGCCACC T A MAGT1 Ensembl:ENSG00000102158 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334874166 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17563,RMVar_hsa_circ_91900,RMVar_hsa_circ_117232,RMVar_hsa_circ_68499,RMVar_hsa_circ_263096,RMVar_hsa_circ_81524,RMVar_hsa_circ_263097,RMVar_hsa_circ_263095,RMVar_hsa_circ_313947,RMVar_hsa_circ_83099,RMVar_hsa_circ_355299,RMVar_hsa_circ_312937,RMVar_hsa_circ_37470,RMVar_hsa_circ_263101,RMVar_hsa_circ_263102 30291 RMVar_ID_30291 Human_SNP_ID_721899960 A-to-I Human chrX - 77851991 77851991 77851991 AGGAGGCTGAGGCAGGAGAATCTCTTGAACCCAGGAGGCAGGGGTTGCAGTGAGCAGAGATCGTG AGGAGGCTGAGGCAGGAGAATCTCTTGAACCCGGGAGGCAGGGGTTGCAGTGAGCAGAGATCGTG T C MAGT1 Ensembl:ENSG00000102158 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1400083624 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17563,RMVar_hsa_circ_91900,RMVar_hsa_circ_117232,RMVar_hsa_circ_68499,RMVar_hsa_circ_263096,RMVar_hsa_circ_81524,RMVar_hsa_circ_263097,RMVar_hsa_circ_263095,RMVar_hsa_circ_313947,RMVar_hsa_circ_83099,RMVar_hsa_circ_355299,RMVar_hsa_circ_312937,RMVar_hsa_circ_37470,RMVar_hsa_circ_263101,RMVar_hsa_circ_263102 30292 RMVar_ID_30292 Human_SNP_ID_721900113 A-to-I Human chrX - 77852870 77852870 77852870 GAATCAGCTGGGCATGGTGGCTCACACCTGTAATCCTAGCACTTTTGGAGGCTGTGATGGGTAGA GAATCAGCTGGGCATGGTGGCTCACACCTGTAGTCCTAGCACTTTTGGAGGCTGTGATGGGTAGA T C MAGT1 Ensembl:ENSG00000102158 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs782668613 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17563,RMVar_hsa_circ_91900,RMVar_hsa_circ_117232,RMVar_hsa_circ_68499,RMVar_hsa_circ_263096,RMVar_hsa_circ_81524,RMVar_hsa_circ_263097,RMVar_hsa_circ_263095,RMVar_hsa_circ_313947,RMVar_hsa_circ_83099,RMVar_hsa_circ_355299,RMVar_hsa_circ_312937,RMVar_hsa_circ_37470,RMVar_hsa_circ_263101,RMVar_hsa_circ_263102 30293 RMVar_ID_30293 Human_SNP_ID_721900978 A-to-I Human chrX - 77858233 77858233 77858233 TGAACCGAGATCCTGCCACTGTGCTTCAGCCTAGGCAACAGAGTGAGACTCCATCTCAAAAATAA TGAACCGAGATCCTGCCACTGTGCTTCAGCCTGGGCAACAGAGTGAGACTCCATCTCAAAAATAA T C MAGT1 Ensembl:ENSG00000102158 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs782620884 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17563,RMVar_hsa_circ_117232,RMVar_hsa_circ_263095,RMVar_hsa_circ_355299,RMVar_hsa_circ_321786 30294 RMVar_ID_30294 Human_SNP_ID_721901461 A-to-I Human chrX - 77861010 77861010 77861010 CAGGCCCAGCTAATTTTTTTCATATTTTTAGTAGGGGCGGGGTTTCTCCATGTTGGTCAGGCTGG CAGGCCCAGCTAATTTTTTTCATATTTTTAGTGGGGGCGGGGTTTCTCCATGTTGGTCAGGCTGG T C MAGT1 Ensembl:ENSG00000102158 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs912780994 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16946125 RMVar_hsa_circ_17563,RMVar_hsa_circ_117232,RMVar_hsa_circ_263095,RMVar_hsa_circ_355299,RMVar_hsa_circ_321786 30295 RMVar_ID_30295 Human_SNP_ID_721902653 A-to-I Human chrX - 77868606 77868606 77868606 TTGAGATGGAGTCTCGCTCTGTTGCCCAGACTAGAGTGCAGTGGCTTGATCTCGGCTCACTGCAA TTGAGATGGAGTCTCGCTCTGTTGCCCAGACTGGAGTGCAGTGGCTTGATCTCGGCTCACTGCAA T C MAGT1 Ensembl:ENSG00000102158 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1016885491 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16946235 Human_Splice_Rec_2220913 RMVar_hsa_circ_17563,RMVar_hsa_circ_117232,RMVar_hsa_circ_263095,RMVar_hsa_circ_355299,RMVar_hsa_circ_321786 30296 RMVar_ID_30296 Human_SNP_ID_721908891 A-to-I Human chrX + 77901794 77901794 77901794 TTACCCAGGCTGGAGTGTAGTGGTGTGATCATAGCTCACTGCATCCTCTAACTCCTGGACTCAAG TTACCCAGGCTGGAGTGTAGTGGTGTGATCATTGCTCACTGCATCCTCTAACTCCTGGACTCAAG A T COX7B Ensembl:ENSG00000131174 Protein coding 5'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027121188 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16946440 Human_Splice_Rec_2220915,Human_Splice_Rec_2220916 RMVar_hsa_circ_97558,RMVar_hsa_circ_263107 30297 RMVar_ID_30297 Human_SNP_ID_721908914 A-to-I Human chrX + 77901925 77901925 77901925 TAATTTTTAATTTTCAATTTTTTTGTAGAGACAGGGTCTCACTATGTTTCACAGACTGGTCTGAA TAATTTTTAATTTTCAATTTTTTTGTAGAGACGGGGTCTCACTATGTTTCACAGACTGGTCTGAA A G COX7B Ensembl:ENSG00000131174 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs782669666 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16967959 RMVar_hsa_circ_97558,RMVar_hsa_circ_263107 30298 RMVar_ID_30298 Human_SNP_ID_721908915 A-to-I Human chrX + 77901936 77901936 77901936 TTTCAATTTTTTTGTAGAGACAGGGTCTCACTATGTTTCACAGACTGGTCTGAAACTCCTGGCCT TTTCAATTTTTTTGTAGAGACAGGGTCTCACTGTGTTTCACAGACTGGTCTGAAACTCCTGGCCT A G COX7B Ensembl:ENSG00000131174 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1464158445 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16946448 RMVar_hsa_circ_97558,RMVar_hsa_circ_263107 30299 RMVar_ID_30299 Human_SNP_ID_721909437 A-to-I Human chrX + 77904531 77904531 77904531 GGGCGTGGTGGTGGGCACCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCCTGAA GGGCGTGGTGGTGGGCACCTGTAGTCCCAGCTGCTTGGGAGGCTGAGGCAGGAGAATCGCCTGAA A G COX7B Ensembl:ENSG00000131174 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1230877747 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97558,RMVar_hsa_circ_107848,RMVar_hsa_circ_263107,RMVar_hsa_circ_263108 30300 RMVar_ID_30300 Human_SNP_ID_721909448 A-to-I Human chrX + 77904604 77904604 77904604 GGGTGGAGGTTGCAGTGAGTTGAGATCGTGCCACTGTACTCTAGCCTGGGCGATAAAGCGAGACT GGGTGGAGGTTGCAGTGAGTTGAGATCGTGCCGCTGTACTCTAGCCTGGGCGATAAAGCGAGACT A G COX7B Ensembl:ENSG00000131174 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946083771 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16946527,Human_RBP_ID_26297796 RMVar_hsa_circ_97558,RMVar_hsa_circ_107848,RMVar_hsa_circ_263107,RMVar_hsa_circ_263108 30301 RMVar_ID_30301 Human_SNP_ID_721923898 A-to-I Human chrX + 77994679 77994679 77994679 TTCCCACCTCAGCCTCCTGAGTGGCTGGGACTATAGGCGTGTACCACCACACCCGGCTAATTTTT TTCCCACCTCAGCCTCCTGAGTGGCTGGGACTGTAGGCGTGTACCACCACACCCGGCTAATTTTT A G ATP7A,PGK1 Ensembl:ENSG00000165240,Ensembl:ENSG00000102144 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs908239438 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12178,RMVar_hsa_circ_40678,RMVar_hsa_circ_302384,RMVar_hsa_circ_352642,RMVar_hsa_circ_281925,RMVar_hsa_circ_28367,RMVar_hsa_circ_43607 30302 RMVar_ID_30302 Human_SNP_ID_721926800 A-to-I Human chrX + 78010778 78010778 78010778 ATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCGTGTTGGCCATACTGCTCTCGAACTCCTGA ATTTTTTGTATTTTTAGTAGAGACGGGGTTTCGCCGTGTTGGCCATACTGCTCTCGAACTCCTGA A G ATP7A,PGK1 Ensembl:ENSG00000165240,Ensembl:ENSG00000102144 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1466854016 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12178,RMVar_hsa_circ_40678,RMVar_hsa_circ_68578,RMVar_hsa_circ_52768,RMVar_hsa_circ_350482,RMVar_hsa_circ_93643,RMVar_hsa_circ_27309,RMVar_hsa_circ_263112,RMVar_hsa_circ_286955,RMVar_hsa_circ_332631,RMVar_hsa_circ_309972,RMVar_hsa_circ_272594,RMVar_hsa_circ_263116,RMVar_hsa_circ_263117,RMVar_hsa_circ_263115 30303 RMVar_ID_30303 Human_SNP_ID_721947153 A-to-I Human chrX + 78120634 78120634 78120634 CTCCCACCTCAGCCTCCCTAGTACCTGGGACTACAGGCATGCATCACCATGCCTGGCTAATTTTT CTCCCACCTCAGCCTCCCTAGTACCTGGGACTGCAGGCATGCATCACCATGCCTGGCTAATTTTT A G PGK1 Ensembl:ENSG00000102144 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1569550876 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100143,RMVar_hsa_circ_27306,RMVar_hsa_circ_117074,RMVar_hsa_circ_121586,RMVar_hsa_circ_263130,RMVar_hsa_circ_263132,RMVar_hsa_circ_106537,RMVar_hsa_circ_116016,RMVar_hsa_circ_119614,RMVar_hsa_circ_263134,RMVar_hsa_circ_263135,RMVar_hsa_circ_263133,RMVar_hsa_circ_324471,RMVar_hsa_circ_263138,RMVar_hsa_circ_83016,RMVar_hsa_circ_263137 30304 RMVar_ID_30304 Human_SNP_ID_721947154 A-to-I Human chrX + 78120636 78120636 78120636 CCCACCTCAGCCTCCCTAGTACCTGGGACTACAGGCATGCATCACCATGCCTGGCTAATTTTTGA CCCACCTCAGCCTCCCTAGTACCTGGGACTACCGGCATGCATCACCATGCCTGGCTAATTTTTGA A C PGK1 Ensembl:ENSG00000102144 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs889608463 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100143,RMVar_hsa_circ_27306,RMVar_hsa_circ_117074,RMVar_hsa_circ_121586,RMVar_hsa_circ_263130,RMVar_hsa_circ_263132,RMVar_hsa_circ_106537,RMVar_hsa_circ_116016,RMVar_hsa_circ_119614,RMVar_hsa_circ_263134,RMVar_hsa_circ_263135,RMVar_hsa_circ_263133,RMVar_hsa_circ_324471,RMVar_hsa_circ_263138,RMVar_hsa_circ_83016,RMVar_hsa_circ_263137 30305 RMVar_ID_30305 Human_SNP_ID_721950894 A-to-I Human chrX - 78138698 78138698 78138698 CAGGCTAGAAGGCAGTGGCGCGATCTTGGCTCACTGCGGCCTCCGCCTCCTGGGTTCAAGCGATT CAGGCTAGAAGGCAGTGGCGCGATCTTGGCTCGCTGCGGCCTCCGCCTCCTGGGTTCAAGCGATT T C TAF9B Ensembl:ENSG00000187325 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1217518521 Functional Loss SNV dbSNP153 33..33 33 - - - 30306 RMVar_ID_30306 Human_SNP_ID_722485030 A-to-I Human chrX + 80529262 80529262 80529262 GCTAATTTCTTCTCACCACTAAATCCAGTATGAATTCATATTGATATTGAAGCTAATGGCGGAGC GCTAATTTCTTCTCACCACTAAATCCAGTATGGATTCATATTGATATTGAAGCTAATGGCGGAGC A G HNRNPH3P1 Ensembl:ENSG00000230247 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1320120804 Functional Loss SNV dbSNP153 33..33 33 - - - 30307 RMVar_ID_30307 Human_SNP_ID_722522405 A-to-I Human chrX + 80710459 80710459 80710459 CTTGGAGAGACATATGTCTAAATTTATGGAATACAATTTAAATGAACTGGTTAAACATGGTCTGC CTTGGAGAGACATATGTCTAAATTTATGGAATGCAATTTAAATGAACTGGTTAAACATGGTCTGC A G AL512504.1 Ensembl:ENSG00000225715 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs751265778 Functional Loss SNV dbSNP153 33..33 33 - - - 30308 RMVar_ID_30308 Human_SNP_ID_722522408 A-to-I Human chrX + 80710492 80710492 80710492 CAATTTAAATGAACTGGTTAAACATGGTCTGCATGCCTGAAGAGAGACAATTCCTGCAGAACAGG CAATTTAAATGAACTGGTTAAACATGGTCTGCTTGCCTGAAGAGAGACAATTCCTGCAGAACAGG A T AL512504.1 Ensembl:ENSG00000225715 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1233781637 Functional Loss SNV dbSNP153 33..33 33 - - - 30309 RMVar_ID_30309 Human_SNP_ID_722536928 A-to-I Human chrX - 80785929 80785929 80785929 CGCTTCTGGGTTCAAGTGATTCTCCTGCGTCAACCTCCCAAGTAACTGGGATTACAGGCTCCTGC CGCTTCTGGGTTCAAGTGATTCTCCTGCGTCAGCCTCCCAAGTAACTGGGATTACAGGCTCCTGC T C BRWD3 Ensembl:ENSG00000165288 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1301463294 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_263155,RMVar_hsa_circ_102092,RMVar_hsa_circ_91537,RMVar_hsa_circ_263162,RMVar_hsa_circ_110568,RMVar_hsa_circ_263165,RMVar_hsa_circ_47435,RMVar_hsa_circ_84710,RMVar_hsa_circ_263170,RMVar_hsa_circ_70001,RMVar_hsa_circ_368054 30310 RMVar_ID_30310 Human_SNP_ID_722537070 A-to-I Human chrX - 80786782 80786782 80786782 GATTAGGCTGGGCGCTGTGGCTTACGCCTGTAATTCCAGCACTTTGGGAGGCCGAGACGGGCACA GATTAGGCTGGGCGCTGTGGCTTACGCCTGTATTTCCAGCACTTTGGGAGGCCGAGACGGGCACA T A BRWD3 Ensembl:ENSG00000165288 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223592925 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23317631 RMVar_hsa_circ_263155,RMVar_hsa_circ_102092,RMVar_hsa_circ_91537,RMVar_hsa_circ_263162,RMVar_hsa_circ_110568,RMVar_hsa_circ_263165,RMVar_hsa_circ_47435,RMVar_hsa_circ_84710,RMVar_hsa_circ_263170,RMVar_hsa_circ_70001,RMVar_hsa_circ_368054 30311 RMVar_ID_30311 Human_SNP_ID_722537748 A-to-I Human chrX - 80790139 80790139 80790139 TCTTGTCACTCAGGCTAGAGTGCATCGGCACAATCTCTGCTCACTGCAACCTCCCCACTCCCTCG TCTTGTCACTCAGGCTAGAGTGCATCGGCACAGTCTCTGCTCACTGCAACCTCCCCACTCCCTCG T C BRWD3 Ensembl:ENSG00000165288 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1225715436 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_263155,RMVar_hsa_circ_102092,RMVar_hsa_circ_91537,RMVar_hsa_circ_263162,RMVar_hsa_circ_110568,RMVar_hsa_circ_263165,RMVar_hsa_circ_47435,RMVar_hsa_circ_84710,RMVar_hsa_circ_263170,RMVar_hsa_circ_70001,RMVar_hsa_circ_368054 30312 RMVar_ID_30312 Human_SNP_ID_723481844 A-to-I Human chrX + 85087996 85087996 85087996 AATTCTAGTGAGATTAAAATCTAAAAATACATATATATATATGTATGTATAAATACATACATATT AATTCTAGTGAGATTAAAATCTAAAAATACATGTATATATATGTATGTATAAATACATACATATT A G APOOL Ensembl:ENSG00000155008 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1314348435 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18155280,Human_RBP_ID_27796316 Human_miRNA_ID_1198661 30313 RMVar_ID_30313 Human_SNP_ID_723481845 A-to-I Human chrX + 85087998 85087998 85087998 TTCTAGTGAGATTAAAATCTAAAAATACATATATATATATGTATGTATAAATACATACATATTTA TTCTAGTGAGATTAAAATCTAAAAATACATATTTATATATGTATGTATAAATACATACATATTTA A T APOOL Ensembl:ENSG00000155008 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs748633842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18155280,Human_RBP_ID_27796316 30314 RMVar_ID_30314 Human_SNP_ID_723481850 A-to-I Human chrX + 85088004 85088004 85088004 TGAGATTAAAATCTAAAAATACATATATATATATGTATGTATAAATACATACATATTTATACATG TGAGATTAAAATCTAAAAATACATATATATATGTGTATGTATAAATACATACATATTTATACATG A G APOOL Ensembl:ENSG00000155008 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1168477536 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18155280,Human_RBP_ID_27796316 30315 RMVar_ID_30315 Human_SNP_ID_723482391 A-to-I Human chrX + 85089304 85089304 85089304 TTTTGTATTTTTGGTAGTGACAGGGTTTCACCATGTTGTCCAGGCTGGTCTCGAACTCCTGAGCT TTTTGTATTTTTGGTAGTGACAGGGTTTCACCGTGTTGTCCAGGCTGGTCTCGAACTCCTGAGCT A G APOOL Ensembl:ENSG00000155008 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs191345667 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_188342 30316 RMVar_ID_30316 Human_SNP_ID_723482618 A-to-I Human chrX + 85090854 85090854 85090854 GTCTTTTAGAGATAGGTATTGCTATGTTGCCCAGGCTGGTCTCAAACTCATGGCCTCAAGCGATC GTCTTTTAGAGATAGGTATTGCTATGTTGCCCGGGCTGGTCTCAAACTCATGGCCTCAAGCGATC A G APOOL Ensembl:ENSG00000155008 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1461406783 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22372733,Human_RBP_ID_26573867 30317 RMVar_ID_30317 Human_SNP_ID_723482628 A-to-I Human chrX + 85090905 85090905 85090905 GGCCTCAAGCGATCCTCCCACCTCAGCCAACCAGACATGAGTGACTGTGCTCAGCCTTTTTTAAA GGCCTCAAGCGATCCTCCCACCTCAGCCAACCGGACATGAGTGACTGTGCTCAGCCTTTTTTAAA A G APOOL Ensembl:ENSG00000155008 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1450259259 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26573867 30318 RMVar_ID_30318 Human_SNP_ID_723482646 A-to-I Human chrX + 85090978 85090978 85090978 GGTATTTGGTATGGCCGGGTATGGTGGCTCACACCTATAATCCCAGCACTTTGGGAGGCCAAGGT GGTATTTGGTATGGCCGGGTATGGTGGCTCACTCCTATAATCCCAGCACTTTGGGAGGCCAAGGT A T APOOL Ensembl:ENSG00000155008 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs926089198 Functional Loss SNV dbSNP153 33..33 33 - - - 30319 RMVar_ID_30319 Human_SNP_ID_723482648 A-to-I Human chrX + 85090982 85090982 85090982 TTTGGTATGGCCGGGTATGGTGGCTCACACCTATAATCCCAGCACTTTGGGAGGCCAAGGTGGGT TTTGGTATGGCCGGGTATGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGT A G APOOL Ensembl:ENSG00000155008 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs937602239 Functional Loss SNV dbSNP153 33..33 33 - - - 30320 RMVar_ID_30320 Human_SNP_ID_723482649 A-to-I Human chrX + 85090982 85090982 85090982 TTTGGTATGGCCGGGTATGGTGGCTCACACCTATAATCCCAGCACTTTGGGAGGCCAAGGTGGGT TTTGGTATGGCCGGGTATGGTGGCTCACACCTTTAATCCCAGCACTTTGGGAGGCCAAGGTGGGT A T APOOL Ensembl:ENSG00000155008 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs937602239 Functional Loss SNV dbSNP153 33..33 33 - - - 30321 RMVar_ID_30321 Human_SNP_ID_723482660 A-to-I Human chrX + 85091058 85091058 85091058 GGTCAGGAGTTTGAGACCAGCCTGACCAACATAGTGAAACCCTGTCTCTACTAAAAACACGCAAA GGTCAGGAGTTTGAGACCAGCCTGACCAACATGGTGAAACCCTGTCTCTACTAAAAACACGCAAA A G APOOL Ensembl:ENSG00000155008 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1298997751 Functional Loss SNV dbSNP153 33..33 33 - - - 30322 RMVar_ID_30322 Human_SNP_ID_723482690 A-to-I Human chrX + 85091231 85091231 85091231 GAGATCGTGCCATTGCACTTCAGCCTGGGCACAAGAACAAAACTCAGTCTCAAAAAATAAATAAT GAGATCGTGCCATTGCACTTCAGCCTGGGCACCAGAACAAAACTCAGTCTCAAAAAATAAATAAT A C APOOL Ensembl:ENSG00000155008 Protein coding 3'UTR GSE47997;GSE38233;GSE38233;GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,24183664,29129909,32596459 RNA-Seq:(High) rs1156821090 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23204825 30323 RMVar_ID_30323 Human_SNP_ID_723482699 A-to-I Human chrX + 85091281 85091281 85091281 CAAAAAATAAATAATAAAAAATAAAGGTATATAATATGTCTTAGATTTGATGAAATATGAGTGTG CAAAAAATAAATAATAAAAAATAAAGGTATATGATATGTCTTAGATTTGATGAAATATGAGTGTG A G APOOL Ensembl:ENSG00000155008 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs762153903 Functional Loss SNV dbSNP153 33..33 33 - - - 30324 RMVar_ID_30324 Human_SNP_ID_723482771 A-to-I Human chrX + 85091788 85091788 85091788 AGGTAGGGAAGCAGTTTACTTGCTAGTTTTTCATAAGTAAGCTCTTCAGAATTTATCTCCAGTAT AGGTAGGGAAGCAGTTTACTTGCTAGTTTTTCGTAAGTAAGCTCTTCAGAATTTATCTCCAGTAT A G APOOL Ensembl:ENSG00000155008 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs972079648 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26574255 30325 RMVar_ID_30325 Human_SNP_ID_723482774 A-to-I Human chrX + 85091810 85091810 85091810 CTAGTTTTTCATAAGTAAGCTCTTCAGAATTTATCTCCAGTATTTGAAATGAATTTTTTTAAACC CTAGTTTTTCATAAGTAAGCTCTTCAGAATTTGTCTCCAGTATTTGAAATGAATTTTTTTAAACC A G APOOL Ensembl:ENSG00000155008 Protein coding 3'UTR GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs141634863 Functional Loss SNV dbSNP153 33..33 33 - - - 30326 RMVar_ID_30326 Human_SNP_ID_723482778 A-to-I Human chrX + 85091876 85091876 85091876 CAGATCTGAATATATTCAAACACCCATATTTCATCAAATCTAAGGCATATCATATACCTTTAATT CAGATCTGAATATATTCAAACACCCATATTTCGTCAAATCTAAGGCATATCATATACCTTTAATT A G APOOL Ensembl:ENSG00000155008 Protein coding 3'UTR GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs1439128406 Functional Loss SNV dbSNP153 33..33 33 - - - 30327 RMVar_ID_30327 Human_SNP_ID_723482781 A-to-I Human chrX + 85091895 85091895 85091895 ACACCCATATTTCATCAAATCTAAGGCATATCATATACCTTTAATTTAAAAAAAAATGCTGAGCA ACACCCATATTTCATCAAATCTAAGGCATATCGTATACCTTTAATTTAAAAAAAAATGCTGAGCA A G APOOL Ensembl:ENSG00000155008 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1386785137 Functional Loss SNV dbSNP153 33..33 33 - - - 30328 RMVar_ID_30328 Human_SNP_ID_723482787 A-to-I Human chrX + 85091915 85091915 85091915 CTAAGGCATATCATATACCTTTAATTTAAAAAAAAATGCTGAGCAGAGTTGCTTATGTCTGGGAG CTAAGGCATATCATATACCTTTAATTTAAAAAGAAATGCTGAGCAGAGTTGCTTATGTCTGGGAG A G APOOL Ensembl:ENSG00000155008 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1437569963 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26573550 30329 RMVar_ID_30329 Human_SNP_ID_723655565 A-to-I Human chrX - 85863096 85863096 85863096 AGAGCAAGACTCTGTCTCACAAAAAAAAAAAAAGGGGGCTGTACATAGGCAGCAAACTAAGCTGC AGAGCAAGACTCTGTCTCACAAAAAAAAAAAAGGGGGGCTGTACATAGGCAGCAAACTAAGCTGC T C CHM Ensembl:ENSG00000188419 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs773925760 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_740400 Human_miRNA_ID_187909 30330 RMVar_ID_30330 Human_SNP_ID_723684688 A-to-I Human chrX - 86025594 86025594 86025594 TAGCTCACTGTAACCTCAAACTCCTGGGCTCAAGTTATCCTCCTGCCTCAGCCTCCTGGGTAACT TAGCTCACTGTAACCTCAAACTCCTGGGCTCAGGTTATCCTCCTGCCTCAGCCTCCTGGGTAACT T C CHM Ensembl:ENSG00000188419 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs745420755 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_785,RMVar_hsa_circ_294525,RMVar_hsa_circ_263227,RMVar_hsa_circ_293570,RMVar_hsa_circ_309279,RMVar_hsa_circ_273505,RMVar_hsa_circ_263228 30331 RMVar_ID_30331 Human_SNP_ID_723684697 A-to-I Human chrX - 86025646 86025646 86025646 TTGACACAGGATCTCACTCTGTTGCCTAGACTATAGTACAGTGGCATGGTAATAGCTCACTGTAA TTGACACAGGATCTCACTCTGTTGCCTAGACTGTAGTACAGTGGCATGGTAATAGCTCACTGTAA T C CHM Ensembl:ENSG00000188419 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1396535877 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22843393 RMVar_hsa_circ_785,RMVar_hsa_circ_294525,RMVar_hsa_circ_263227,RMVar_hsa_circ_293570,RMVar_hsa_circ_309279,RMVar_hsa_circ_273505,RMVar_hsa_circ_263228 30332 RMVar_ID_30332 Human_SNP_ID_723695871 A-to-I Human chrX - 86085073 86085073 86085073 CTCAAGGACTGTGAAGAATGTATCCAGCTAGAACCGACCTTCATCAAGGGTTATACACGGAAAGC CTCAAGGACTGTGAAGAATGTATCCAGCTAGAGCCGACCTTCATCAAGGGTTATACACGGAAAGC T C STIP1P3 Ensembl:ENSG00000225536 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879150610 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8277299,Human_RBP_ID_18543630 Human_miRNA_ID_1882088 30333 RMVar_ID_30333 Human_SNP_ID_723695873 A-to-I Human chrX - 86085076 86085076 86085076 GCACTCAAGGACTGTGAAGAATGTATCCAGCTAGAACCGACCTTCATCAAGGGTTATACACGGAA GCACTCAAGGACTGTGAAGAATGTATCCAGCTGGAACCGACCTTCATCAAGGGTTATACACGGAA T C STIP1P3 Ensembl:ENSG00000225536 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878875711 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8277299,Human_RBP_ID_18543630 Human_miRNA_ID_1882088 30334 RMVar_ID_30334 Human_SNP_ID_723695876 A-to-I Human chrX - 86085091 86085091 86085091 CCTGGATTCCAGCTGGCACTCAAGGACTGTGAAGAATGTATCCAGCTAGAACCGACCTTCATCAA CCTGGATTCCAGCTGGCACTCAAGGACTGTGAGGAATGTATCCAGCTAGAACCGACCTTCATCAA T C STIP1P3 Ensembl:ENSG00000225536 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879202084 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1822502,Human_miRNA_ID_1847687,Human_miRNA_ID_1848034 30335 RMVar_ID_30335 Human_SNP_ID_723695922 A-to-I Human chrX - 86085258 86085258 86085258 CTGGCCTACATAAACCCCGACCTGGCTTTAGAAGAGAAGAACAAAGGCAACGAGTGTTTTCAGAA CTGGCCTACATAAACCCCGACCTGGCTTTAGAGGAGAAGAACAAAGGCAACGAGTGTTTTCAGAA T C STIP1P3 Ensembl:ENSG00000225536 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878991042 Functional Loss SNV dbSNP153 33..33 33 - - - 30336 RMVar_ID_30336 Human_SNP_ID_723695923 A-to-I Human chrX - 86085261 86085261 86085261 CGGCTGGCCTACATAAACCCCGACCTGGCTTTAGAAGAGAAGAACAAAGGCAACGAGTGTTTTCA CGGCTGGCCTACATAAACCCCGACCTGGCTTTGGAAGAGAAGAACAAAGGCAACGAGTGTTTTCA T C STIP1P3 Ensembl:ENSG00000225536 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878915161 Functional Loss SNV dbSNP153 33..33 33 - - - 30337 RMVar_ID_30337 Human_SNP_ID_723695929 A-to-I Human chrX - 86085294 86085294 86085294 CAGCAGGCAGAGAAAATCCTGAAGGAGCAAGAACGGCTGGCCTACATAAACCCCGACCTGGCTTT CAGCAGGCAGAGAAAATCCTGAAGGAGCAAGAGCGGCTGGCCTACATAAACCCCGACCTGGCTTT T C STIP1P3 Ensembl:ENSG00000225536 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878963308 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17443769,Human_RBP_ID_17556337 30338 RMVar_ID_30338 Human_SNP_ID_323721642 A-to-I Human chr7 + 64434121 64434121 64434121 AGAAGACAAGCTAAAAATGATTTGGGAATATCAGCAAATGATTGAGACTGAGCTAAAGTTACTCT AGAAGACAAGCTAAAAATGATTTGGGAATATCGGCAAATGATTGAGACTGAGCTAAAGTTACTCT A G YWHAEP1 Ensembl:ENSG00000232727 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1211899037 Functional Loss SNV dbSNP153 33..33 33 - - - 30339 RMVar_ID_30339 Human_SNP_ID_323738627 A-to-I Human chr7 - 64507630 64507630 64507630 AATATGGATGGCTCACACCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACGTGAA AATATGGATGGCTCACACCTGTAATCCCAGCTGCTCGGGAGGCTGAGGCAGGAGAATCACGTGAA T C RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1298611209 Functional Loss SNV dbSNP153 33..33 33 - - - 30340 RMVar_ID_30340 Human_SNP_ID_323743801 A-to-I Human chr7 - 64527233 64527233 64527233 TTTGTTTATTTATTTATTTATTTATTTGAGACAGAATCTTGCTCTTATTGCCCAGGCTGGAGTGC TTTGTTTATTTATTTATTTATTTATTTGAGACGGAATCTTGCTCTTATTGCCCAGGCTGGAGTGC T C ZNF680 Ensembl:ENSG00000173041 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs960365940 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3096309,Human_RBP_ID_7748246,Human_RBP_ID_16186084 RMVar_hsa_circ_76458,RMVar_hsa_circ_269045,RMVar_hsa_circ_245260,RMVar_hsa_circ_245257,RMVar_hsa_circ_245259 30341 RMVar_ID_30341 Human_SNP_ID_323745993 A-to-I Human chr7 - 64536903 64536903 64536903 ATCATGTCTAGCTATTTTTTTTGATTATTTGTAGGGACAGGGCCTCACTGTGTTACCTAGGCTGG ATCATGTCTAGCTATTTTTTTTGATTATTTGTGGGGACAGGGCCTCACTGTGTTACCTAGGCTGG T C ZNF680 Ensembl:ENSG00000173041 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1413417803 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7748298,Human_RBP_ID_16186274 RMVar_hsa_circ_76458,RMVar_hsa_circ_269045,RMVar_hsa_circ_245260,RMVar_hsa_circ_245257,RMVar_hsa_circ_245259 30342 RMVar_ID_30342 Human_SNP_ID_323746012 A-to-I Human chr7 - 64536970 64536970 64536970 AGCCTCCTGGGCTCAAGTGATCCTTCCACCTCAGCTCCCCGTGTAGCTGAAACTACAGACATGCA AGCCTCCTGGGCTCAAGTGATCCTTCCACCTCGGCTCCCCGTGTAGCTGAAACTACAGACATGCA T C ZNF680 Ensembl:ENSG00000173041 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277180372 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24220697 RMVar_hsa_circ_76458,RMVar_hsa_circ_269045,RMVar_hsa_circ_245260,RMVar_hsa_circ_245257,RMVar_hsa_circ_245259 30343 RMVar_ID_30343 Human_SNP_ID_323747488 A-to-I Human chr7 - 64542822 64542822 64542822 TGGTGGCAGGTTCCTATAATCCCAGCTACCCAAAAGGCTGAGGCAGGAGAATTGCTTTAACACAG TGGTGGCAGGTTCCTATAATCCCAGCTACCCAGAAGGCTGAGGCAGGAGAATTGCTTTAACACAG T C ZNF680 Ensembl:ENSG00000173041 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1236885741 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76458,RMVar_hsa_circ_269045,RMVar_hsa_circ_245260,RMVar_hsa_circ_245257,RMVar_hsa_circ_245259 30344 RMVar_ID_30344 Human_SNP_ID_323751979 A-to-I Human chr7 - 64560251 64560241 64560251 AAATTAGCCGGGCGTGGTGGTACATGCCTGTAATTCCAGCTACTTGGGAGGCTGAAGCAGGAAAA AAATTAGCCGGGCGTGGTGGTACATGCCTGTA__________CTTGGGAGGCTGAAGCAGGAAAA GTAGCTGGAAT G ZNF680 Ensembl:ENSG00000173041 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1306319952 Functional Loss DEL dbSNP153 33..42 33 - - - 30345 RMVar_ID_30345 Human_SNP_ID_323752040 A-to-I Human chr7 - 64560461 64560461 64560461 CTTTTAGAATGCTAGCTATCTAGGGAAAAAATAGAGAAAATCTCTTCTCCATTTTGGCTTTAGAA CTTTTAGAATGCTAGCTATCTAGGGAAAAAATTGAGAAAATCTCTTCTCCATTTTGGCTTTAGAA T A ZNF680 Ensembl:ENSG00000173041 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1245130385 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7748469 30346 RMVar_ID_30346 Human_SNP_ID_323752078 A-to-I Human chr7 - 64560672 64560672 64560672 GAGTAGCTGAGACTACAGGCGCTAGCCACCACACTCAGCTAATTTTTGTATTTTTAGTAGGGATG GAGTAGCTGAGACTACAGGCGCTAGCCACCACGCTCAGCTAATTTTTGTATTTTTAGTAGGGATG T C ZNF680 Ensembl:ENSG00000173041 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1002851105 Functional Loss SNV dbSNP153 33..33 33 - - - 30347 RMVar_ID_30347 Human_SNP_ID_323779521 A-to-I Human chr7 + 64669737 64669737 64669737 TTGAATCTGGGAGGCAGAGGTTGCAGTGAGCCAAGAGTGTACCACTGCACTCCAGGCTGGGCAAC TTGAATCTGGGAGGCAGAGGTTGCAGTGAGCCTAGAGTGTACCACTGCACTCCAGGCTGGGCAAC A T ZNF107 Ensembl:ENSG00000196247 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1424665647 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97353,RMVar_hsa_circ_245265 30348 RMVar_ID_30348 Human_SNP_ID_323819096 A-to-I Human chr7 + 64819853 64819853 64819853 TCAGGATTTTGGGAGGCCAAGACAAGAGGATTACTTGAGCATGAAAGTTTGAGACCAGCCCGGGA TCAGGATTTTGGGAGGCCAAGACAAGAGGATTGCTTGAGCATGAAAGTTTGAGACCAGCCCGGGA A G ZNF138 Ensembl:ENSG00000197008 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1244783851 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16188348 RMVar_hsa_circ_376723,RMVar_hsa_circ_352318,RMVar_hsa_circ_245272,RMVar_hsa_circ_245273,RMVar_hsa_circ_72519 30349 RMVar_ID_30349 Human_SNP_ID_323820110 A-to-I Human chr7 + 64823513 64823513 64823513 ATGCACTACCATGTTCAACTAATTTTTTGATTATTTGTAGGGACAAGACATCACTATGTTGCCCA ATGCACTACCATGTTCAACTAATTTTTTGATTGTTTGTAGGGACAAGACATCACTATGTTGCCCA A G ZNF138 Ensembl:ENSG00000197008 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1367520289 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16188419 RMVar_hsa_circ_376723,RMVar_hsa_circ_245272,RMVar_hsa_circ_245273,RMVar_hsa_circ_72519 30350 RMVar_ID_30350 Human_SNP_ID_323845992 A-to-I Human chr7 + 64922823 64922823 64922823 CCTGTCTCTACTAAAAATACGAAACATTAGCCAGGTGTGGTGGTGCATGCCTGTAATCCCAGCTT CCTGTCTCTACTAAAAATACGAAACATTAGCCGGGTGTGGTGGTGCATGCCTGTAATCCCAGCTT A G ZNF273 Ensembl:ENSG00000198039 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs550505372 Functional Loss SNV dbSNP153 33..33 33 - - - 30351 RMVar_ID_30351 Human_SNP_ID_323868218 A-to-I Human chr7 - 65002609 65002609 65002609 TAAGAAGTATTTTAGGCTGGGCACAATGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAG TAAGAAGTATTTTAGGCTGGGCACAATGGCTCGTGCCTGTAATCCCAGCACTTTGGGAGGCCAAG T C ZNF117,ERV3-1 Ensembl:ENSG00000152926,Ensembl:ENSG00000213462 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs891794017 Functional Loss SNV dbSNP153 33..33 33 - - - 30352 RMVar_ID_30352 Human_SNP_ID_323880862 A-to-I Human chr7 + 65046108 65046108 65046108 CTGGGTCTACAGTTGCGCACCCCACCATGCCTAGCTAATTTTTTCTATTTTTCATAGTGACCAGG CTGGGTCTACAGTTGCGCACCCCACCATGCCTGGCTAATTTTTTCTATTTTTCATAGTGACCAGG A G CCT6P3 Ensembl:ENSG00000234585 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs891587916 Functional Loss SNV dbSNP153 33..33 33 - - - 30353 RMVar_ID_30353 Human_SNP_ID_323888366 A-to-I Human chr7 - 65078282 65078282 65078282 TCACTACAGCCTCTGCCCCCGTGGGCTCAAGCAGTCCTCCCACCTCAGCCTCCTAAGAGCTGGGA TCACTACAGCCTCTGCCCCCGTGGGCTCAAGCGGTCCTCCCACCTCAGCCTCCTAAGAGCTGGGA T C lnc-ERV3-1-1,lnc-ERV3-1-1:2,lnc-ERV3-1-1:3,lnc-ERV3-1-1:4 RNACentral:URS0000D5E060,RNACentral:URS00008C3D30,RNACentral:URS00008C0E81,RNACentral:URS00008C2D62 lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1400117757 Functional Loss SNV dbSNP153 33..33 33 - - - 30354 RMVar_ID_30354 Human_SNP_ID_323894917 A-to-I Human chr7 + 65103551 65103551 65103551 CTTACTGCAACCCCCAACTCCCGGGTTCCAGCATTTCTCTGCCTCAGCCTCCTGAGTAGCTGGGA CTTACTGCAACCCCCAACTCCCGGGTTCCAGCGTTTCTCTGCCTCAGCCTCCTGAGTAGCTGGGA A G lnc-ZNF273-7 RNACentral:URS00008BF92D lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1242280414 Functional Loss SNV dbSNP153 33..33 33 - - - 30355 RMVar_ID_30355 Human_SNP_ID_324042683 A-to-I Human chr7 - 65722821 65722821 65722821 TGAGGCAGGAGAATTGCTTGAACCCAGGAGGCAGAGGTTGCAGCGAGCTGAGATCACATCACTGC TGAGGCAGGAGAATTGCTTGAACCCAGGAGGCTGAGGTTGCAGCGAGCTGAGATCACATCACTGC T A AC073107.1 Ensembl:ENSG00000272693 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1267505848 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17429722 30356 RMVar_ID_30356 Human_SNP_ID_324042685 A-to-I Human chr7 - 65722828 65722828 65722828 GGGAGGCTGAGGCAGGAGAATTGCTTGAACCCAGGAGGCAGAGGTTGCAGCGAGCTGAGATCACA GGGAGGCTGAGGCAGGAGAATTGCTTGAACCCGGGAGGCAGAGGTTGCAGCGAGCTGAGATCACA T C AC073107.1 Ensembl:ENSG00000272693 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs550067640 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17429722 30357 RMVar_ID_30357 Human_SNP_ID_324042695 A-to-I Human chr7 - 65722874 65722874 65722874 AAAATTAGCCAGGCTTGATGGTGGGCACCTGTAATCCCAGCTGCTTGGGAGGCTGAGGCAGGAGA AAAATTAGCCAGGCTTGATGGTGGGCACCTGTCATCCCAGCTGCTTGGGAGGCTGAGGCAGGAGA T G AC073107.1 Ensembl:ENSG00000272693 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs376620576 Functional Loss SNV dbSNP153 33..33 33 - - - 30358 RMVar_ID_30358 Human_SNP_ID_324044114 A-to-I Human chr7 - 65728673 65728673 65728673 GGAGTGCAATGGCGCAATCTCGGCTCACCGCAACCTCTGCCTTCTGGGTTTAAGCAATTCTCCTG GGAGTGCAATGGCGCAATCTCGGCTCACCGCATCCTCTGCCTTCTGGGTTTAAGCAATTCTCCTG T A AC073107.1 Ensembl:ENSG00000272693 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1279591228 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17431291 30359 RMVar_ID_30359 Human_SNP_ID_324044115 A-to-I Human chr7 - 65728673 65728673 65728673 GGAGTGCAATGGCGCAATCTCGGCTCACCGCAACCTCTGCCTTCTGGGTTTAAGCAATTCTCCTG GGAGTGCAATGGCGCAATCTCGGCTCACCGCAGCCTCTGCCTTCTGGGTTTAAGCAATTCTCCTG T C AC073107.1 Ensembl:ENSG00000272693 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1279591228 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17431291 30360 RMVar_ID_30360 Human_SNP_ID_324044488 A-to-I Human chr7 - 65730231 65730231 65730231 AATACTTGGACTAGCTGGGCATGGTGGTTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGC AATACTTGGACTAGCTGGGCATGGTGGTTCACCCCTGTAATCCCAGCACTTTGGGAGGCTGAGGC T G AC073107.1 Ensembl:ENSG00000272693 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879954965 Functional Loss SNV dbSNP153 33..33 33 - - - 30361 RMVar_ID_30361 Human_SNP_ID_324045837 A-to-I Human chr7 - 65736171 65736171 65736171 ACTTGGGAGATTGAGGCAGGAGAATCACTTGAACCCAGGAGGCAGAGGTTGCAGTCAGCCGAGAT ACTTGGGAGATTGAGGCAGGAGAATCACTTGATCCCAGGAGGCAGAGGTTGCAGTCAGCCGAGAT T A AC073107.1 Ensembl:ENSG00000272693 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1344147482 Functional Loss SNV dbSNP153 33..33 33 - - - 30362 RMVar_ID_30362 Human_SNP_ID_324045838 A-to-I Human chr7 - 65736171 65736171 65736171 ACTTGGGAGATTGAGGCAGGAGAATCACTTGAACCCAGGAGGCAGAGGTTGCAGTCAGCCGAGAT ACTTGGGAGATTGAGGCAGGAGAATCACTTGAGCCCAGGAGGCAGAGGTTGCAGTCAGCCGAGAT T C AC073107.1 Ensembl:ENSG00000272693 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1344147482 Functional Loss SNV dbSNP153 33..33 33 - - - 30363 RMVar_ID_30363 Human_SNP_ID_324045840 A-to-I Human chr7 - 65736177 65736177 65736177 CCAGTTACTTGGGAGATTGAGGCAGGAGAATCACTTGAACCCAGGAGGCAGAGGTTGCAGTCAGC CCAGTTACTTGGGAGATTGAGGCAGGAGAATCGCTTGAACCCAGGAGGCAGAGGTTGCAGTCAGC T C AC073107.1 Ensembl:ENSG00000272693 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1382959981 Functional Loss SNV dbSNP153 33..33 33 - - - 30364 RMVar_ID_30364 Human_SNP_ID_324046278 A-to-I Human chr7 - 65737806 65737806 65737806 ATTATTTGTTTATTTATTTATTTTGAGATGGAATCTTTCTCCGTCACCAGGCTGGAGTGCAGTAG ATTATTTGTTTATTTATTTATTTTGAGATGGAGTCTTTCTCCGTCACCAGGCTGGAGTGCAGTAG T C AC073107.1 Ensembl:ENSG00000272693 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1410720337 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18520628,Human_RBP_ID_24517050 30365 RMVar_ID_30365 Human_SNP_ID_324046529 A-to-I Human chr7 - 65738829 65738829 65738829 CCTTAGCCTCCCAAAGTGGTTGGATTATAGGCATGAGCTACCGTGCTGGCCAAAATAGAATGTTA CCTTAGCCTCCCAAAGTGGTTGGATTATAGGCGTGAGCTACCGTGCTGGCCAAAATAGAATGTTA T C AC073107.1 Ensembl:ENSG00000272693 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432153057 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16192139 30366 RMVar_ID_30366 Human_SNP_ID_324046531 A-to-I Human chr7 - 65738835 65738835 65738835 CTCTTGCCTTAGCCTCCCAAAGTGGTTGGATTATAGGCATGAGCTACCGTGCTGGCCAAAATAGA CTCTTGCCTTAGCCTCCCAAAGTGGTTGGATTGTAGGCATGAGCTACCGTGCTGGCCAAAATAGA T C AC073107.1 Ensembl:ENSG00000272693 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1562888723 Functional Loss SNV dbSNP153 33..33 33 - - - 30367 RMVar_ID_30367 Human_SNP_ID_324046842 A-to-I Human chr7 - 65739498 65739494 65739498 TTGCCCAGGCTGAAGTGCAGTGGCACGATCTCAGCTCACTGCAACCTCCACCTCCAGGGTTCAAG TTGCCCAGGCTGAAGTGCAGTGGCACGATCTC____CACTGCAACCTCCACCTCCAGGGTTCAAG GAGCT G AC073107.1 Ensembl:ENSG00000272693 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1554372273 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_16192144 30368 RMVar_ID_30368 Human_SNP_ID_324047155 A-to-I Human chr7 - 65740960 65740960 65740960 ACCTGGATAATTTTTTGATGTTTCATGGAGACAGTGCTTCACTTTGTTGCCTATGCTGGTCTTGA ACCTGGATAATTTTTTGATGTTTCATGGAGACGGTGCTTCACTTTGTTGCCTATGCTGGTCTTGA T C AC073107.1 Ensembl:ENSG00000272693 Pseudogene intron GSE38233;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,32596459 RNA-Seq:(High) rs1554372475 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96827,RMVar_hsa_circ_245290 30369 RMVar_ID_30369 Human_SNP_ID_324047164 A-to-I Human chr7 - 65741007 65741007 65741007 CTGCCTCAGCCTCCCGTGTAGCTGGGACCACAAGCACTCGCCATCACACCTGGATAATTTTTTGA CTGCCTCAGCCTCCCGTGTAGCTGGGACCACAGGCACTCGCCATCACACCTGGATAATTTTTTGA T C AC073107.1 Ensembl:ENSG00000272693 Pseudogene intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1200376694 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16192191,Human_RBP_ID_17431303,Human_RBP_ID_18541079 RMVar_hsa_circ_96827,RMVar_hsa_circ_245290 30370 RMVar_ID_30370 Human_SNP_ID_324047389 A-to-I Human chr7 - 65741915 65741915 65741915 GCCTTGAACTCCTGGCCTCACGTGATTCTCCTACCTCAGCCTACCCAGTAGCTGGGACTACAGGT GCCTTGAACTCCTGGCCTCACGTGATTCTCCTCCCTCAGCCTACCCAGTAGCTGGGACTACAGGT T G AC073107.1 Ensembl:ENSG00000272693 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1554372584 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17429759 30371 RMVar_ID_30371 Human_SNP_ID_324048239 A-to-I Human chr7 - 65745304 65745304 65745304 CGGCTCACTGTAACCTCCGCCTTCTAGGTTCAAGTGATTCTTCTGCATCAGCCTCCAGGCACACG CGGCTCACTGTAACCTCCGCCTTCTAGGTTCAGGTGATTCTTCTGCATCAGCCTCCAGGCACACG T C AC073107.1 Ensembl:ENSG00000272693 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1225342220 Functional Loss SNV dbSNP153 33..33 33 - - - 30372 RMVar_ID_30372 Human_SNP_ID_324049839 A-to-I Human chr7 + 65751064 65751064 65751064 TGGGCGCGCCGACTTTTCCGGAAGATCCGGATAGTGCATCCCGGCCACGGCGCGCCTGCTCTGGG TGGGCGCGCCGACTTTTCCGGAAGATCCGGATGGTGCATCCCGGCCACGGCGCGCCTGCTCTGGG A G lnc-VKORC1L1-7,RF00017-4520 RNACentral:URS00008B21F7,RNACentral:URS000099C2D3 lincRNA,SRP RNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs535697290 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2027127,Human_miRNA_ID_2027128 30373 RMVar_ID_30373 Human_SNP_ID_324054631 A-to-I Human chr7 - 65769356 65769356 65769356 AAAATAACCTGGGCATTATAGTGCACACCTGTAGTCCGAGCTACTCAGGAGGCTGAGATGGGAGG AAAATAACCTGGGCATTATAGTGCACACCTGTTGTCCGAGCTACTCAGGAGGCTGAGATGGGAGG T A AC073107.1 Ensembl:ENSG00000272693 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1435940463 Functional Loss SNV dbSNP153 33..33 33 - - - 30374 RMVar_ID_30374 Human_SNP_ID_324058409 A-to-I Human chr7 + 65783933 65783933 65783933 TCAGTTAGCGGGGCGTGGTGGCATGCACCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGA TCAGTTAGCGGGGCGTGGTGGCATGCACCTGTGATCCCAGCTACTTGGGAGGCTGAGGCAGGAGA A G GTF2IP5 Ensembl:ENSG00000224316 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1262049965 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17428969 30375 RMVar_ID_30375 Human_SNP_ID_324072812 A-to-I Human chr7 + 65837265 65837265 65837265 AGGGTCTCACTGTGTTGTCCAGGCCAATCTCTAGCTCCCGGCCTCAATCAGTCCTCCTGTGTTGG AGGGTCTCACTGTGTTGTCCAGGCCAATCTCTGGCTCCCGGCCTCAATCAGTCCTCCTGTGTTGG A G lnc-VKORC1L1-2,RF00017-4520,lnc-VKORC1L1-4 RNACentral:URS00008BDB22,RNACentral:URS000099C2D3,RNACentral:URS00008BED25 lincRNA,SRP RNA,lincRNA intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs759445009 Functional Loss SNV dbSNP153 33..33 33 - - - 30376 RMVar_ID_30376 Human_SNP_ID_324074841 A-to-I Human chr7 + 65844522 65844522 65844522 TATAGAAAAGTACAAAGCACGCCGGGTGCTATAGCTCACACCTGTAATCCCAGCACTTTGGGAAG TATAGAAAAGTACAAAGCACGCCGGGTGCTATGGCTCACACCTGTAATCCCAGCACTTTGGGAAG A G lnc-VKORC1L1-2,RF00017-4520,lnc-VKORC1L1-4 RNACentral:URS00008BDB22,RNACentral:URS000099C2D3,RNACentral:URS00008BED25 lincRNA,SRP RNA,lincRNA intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs927116489 Functional Loss SNV dbSNP153 33..33 33 - - - 30377 RMVar_ID_30377 Human_SNP_ID_324082411 A-to-I Human chr7 + 65874436 65874436 65874436 GTCAGGCTGGTCTCGAACTCCTGACCTCAGGTAATCCACCCACCTCTGCCTTCCAAAGTGCTGGG GTCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCCACCCACCTCTGCCTTCCAAAGTGCTGGG A G VKORC1L1 Ensembl:ENSG00000196715 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1284519809 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18519982,Human_RBP_ID_23198174 30378 RMVar_ID_30378 Human_SNP_ID_324083373 A-to-I Human chr7 + 65878308 65878308 65878308 TGTCTACTAAAAATACAAAAAATTAGCCGGGCATGGTGGTGGGCACCTGTAATTCCAGCTACTCG TGTCTACTAAAAATACAAAAAATTAGCCGGGCGTGGTGGTGGGCACCTGTAATTCCAGCTACTCG A G VKORC1L1 Ensembl:ENSG00000196715 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs950741662 Functional Loss SNV dbSNP153 33..33 33 - - - 30379 RMVar_ID_30379 Human_SNP_ID_324083858 A-to-I Human chr7 + 65879963 65879963 65879963 AGCCTCAACCTCCCTGGGTCAAGTGATCCTCCAACCTCAGCTTCCTGAGTAGCTGGGTCTACAGT AGCCTCAACCTCCCTGGGTCAAGTGATCCTCCCACCTCAGCTTCCTGAGTAGCTGGGTCTACAGT A C VKORC1L1 Ensembl:ENSG00000196715 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs377274384 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_102 30380 RMVar_ID_30380 Human_SNP_ID_324083859 A-to-I Human chr7 + 65879963 65879963 65879963 AGCCTCAACCTCCCTGGGTCAAGTGATCCTCCAACCTCAGCTTCCTGAGTAGCTGGGTCTACAGT AGCCTCAACCTCCCTGGGTCAAGTGATCCTCCGACCTCAGCTTCCTGAGTAGCTGGGTCTACAGT A G VKORC1L1 Ensembl:ENSG00000196715 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs377274384 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_102 30381 RMVar_ID_30381 Human_SNP_ID_324083861 A-to-I Human chr7 + 65879991 65879991 65879991 CTCCAACCTCAGCTTCCTGAGTAGCTGGGTCTACAGTTGCACACCCCACCATGCCTAGCTAATTT CTCCAACCTCAGCTTCCTGAGTAGCTGGGTCTGCAGTTGCACACCCCACCATGCCTAGCTAATTT A G VKORC1L1 Ensembl:ENSG00000196715 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs931402098 Functional Loss SNV dbSNP153 33..33 33 - - - 30382 RMVar_ID_30382 Human_SNP_ID_324083870 A-to-I Human chr7 + 65880015 65880015 65880015 CTGGGTCTACAGTTGCACACCCCACCATGCCTAGCTAATTTTTTCTATTTTTCATAGTGACGAGG CTGGGTCTACAGTTGCACACCCCACCATGCCTGGCTAATTTTTTCTATTTTTCATAGTGACGAGG A G VKORC1L1 Ensembl:ENSG00000196715 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1156289936 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22835360 30383 RMVar_ID_30383 Human_SNP_ID_324089217 A-to-I Human chr7 + 65900812 65900801 65900813 GGGTGACAGAGCAAGACTCTGCTAAAAATAATAATAAAAATAATAATAATAGAAGTACATACATA GGGTGACAGAGCAAGACTCTGC____________TAAAAATAATAATAATAGAAGTACATACATA CTAAAAATAATAA C VKORC1L1 Ensembl:ENSG00000196715 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1182316470 Functional Loss DEL dbSNP153 23..34 33 - - - 30384 RMVar_ID_30384 Human_SNP_ID_324089224 A-to-I Human chr7 + 65900821 65900814 65900822 AGCAAGACTCTGCTAAAAATAATAATAAAAATAATAATAATAGAAGTACATACATAAACTTTAAA AGCAAGACTCTGCTAAAAATAATAAT________TAATAATAGAAGTACATACATAAACTTTAAA TAAAAATAA T VKORC1L1 Ensembl:ENSG00000196715 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs962824075 Functional Loss DEL dbSNP153 27..34 33 - - - Human_RBP_ID_3097572 30385 RMVar_ID_30385 Human_SNP_ID_324090071 A-to-I Human chr7 + 65904232 65904232 65904232 AACCTTAGTCAGGTTATTTATTTATTTGAGACAGAGTATCACTTTGTTGCCCAGGGTGGAGTACA AACCTTAGTCAGGTTATTTATTTATTTGAGACCGAGTATCACTTTGTTGCCCAGGGTGGAGTACA A C VKORC1L1 Ensembl:ENSG00000196715 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444519346 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7750545 30386 RMVar_ID_30386 Human_SNP_ID_324098769 A-to-I Human chr7 + 65941315 65941315 65941315 TCTTCTTTTTTTAGGTAGCGACAGAGTCTCATAATGTTGCCCAGGCTGATCTTGAACTCCTGGGC TCTTCTTTTTTTAGGTAGCGACAGAGTCTCATGATGTTGCCCAGGCTGATCTTGAACTCCTGGGC A G VKORC1L1 Ensembl:ENSG00000196715 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs948232087 Functional Loss SNV dbSNP153 33..33 33 - - - 30387 RMVar_ID_30387 Human_SNP_ID_324103679 A-to-I Human chr7 - 65961332 65961332 65961332 CCCAGTAGTTTGAGACCAGCCTGGACAACATAATGAGACCTTGTCTTTACTAAAAAATAAAAATA CCCAGTAGTTTGAGACCAGCCTGGACAACATATTGAGACCTTGTCTTTACTAAAAAATAAAAATA T A GUSB Ensembl:ENSG00000169919 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1395140508 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91111,RMVar_hsa_circ_101593,RMVar_hsa_circ_85354,RMVar_hsa_circ_245298,RMVar_hsa_circ_245299,RMVar_hsa_circ_245297 30388 RMVar_ID_30388 Human_SNP_ID_324103780 A-to-I Human chr7 - 65961817 65961817 65961817 TTGTATTTTTAGTAGAGATGAGGTTTCACCATATTGTCCAGGCTGGTCTTAATCTCCTGACCTTG TTGTATTTTTAGTAGAGATGAGGTTTCACCATGTTGTCCAGGCTGGTCTTAATCTCCTGACCTTG T C GUSB Ensembl:ENSG00000169919 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1488022951 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91111,RMVar_hsa_circ_101593,RMVar_hsa_circ_85354,RMVar_hsa_circ_245298,RMVar_hsa_circ_245299,RMVar_hsa_circ_245297 30389 RMVar_ID_30389 Human_SNP_ID_324103820 A-to-I Human chr7 - 65961919 65961919 65961919 CAGCTCACTGCAACCTCTGCGTCCTGGGTTCAAGCGATTCTCCTGCCCCAGCCTCCTGAGTAGCT CAGCTCACTGCAACCTCTGCGTCCTGGGTTCACGCGATTCTCCTGCCCCAGCCTCCTGAGTAGCT T G GUSB Ensembl:ENSG00000169919 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1331712319 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91111,RMVar_hsa_circ_101593,RMVar_hsa_circ_85354,RMVar_hsa_circ_245298,RMVar_hsa_circ_245299,RMVar_hsa_circ_245297 30390 RMVar_ID_30390 Human_SNP_ID_324103997 A-to-I Human chr7 - 65962710 65962710 65962710 GCGCCACCACACCCGGCTAATTTTGTATTTTTAGTAGAGACGGGGTTTCTCCATGTTGGTCAGGC GCGCCACCACACCCGGCTAATTTTGTATTTTTGGTAGAGACGGGGTTTCTCCATGTTGGTCAGGC T C GUSB Ensembl:ENSG00000169919 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1350141885 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91111,RMVar_hsa_circ_101593,RMVar_hsa_circ_85354,RMVar_hsa_circ_245298,RMVar_hsa_circ_245299,RMVar_hsa_circ_245297 30391 RMVar_ID_30391 Human_SNP_ID_324104089 A-to-I Human chr7 - 65963010 65963010 65963010 CTACTAAAAATACAAAATTAGCCGGGTGTGGTAGCGCATGCCTGTAATGCCAGCCACTTGGGAGA CTACTAAAAATACAAAATTAGCCGGGTGTGGTGGCGCATGCCTGTAATGCCAGCCACTTGGGAGA T C GUSB Ensembl:ENSG00000169919 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1271743011 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91111,RMVar_hsa_circ_101593,RMVar_hsa_circ_85354,RMVar_hsa_circ_245298,RMVar_hsa_circ_245299,RMVar_hsa_circ_245297 30392 RMVar_ID_30392 Human_SNP_ID_324104249 A-to-I Human chr7 + 65963685 65963685 65963685 CGCCTGCCTCAGCCTCCCAAGCAGCTGAGACTACAGGCACACACCACCACGCCTAGCTAATCTGT CGCCTGCCTCAGCCTCCCAAGCAGCTGAGACTGCAGGCACACACCACCACGCCTAGCTAATCTGT A G lnc-VKORC1L1-2,RF00017-4520,RF00017-4552 RNACentral:URS00008BDB22,RNACentral:URS000099C2D3,RNACentral:URS0000973F83 lincRNA,SRP RNA,SRP RNA intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1246408897 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118631,RMVar_hsa_circ_245295 30393 RMVar_ID_30393 Human_SNP_ID_324104741 A-to-I Human chr7 - 65965662 65965661 65965662 AGTTGGGCATGGTTATGAGTGCTTGTAGTCCAAGCCACTTGGGAGGCTGAGGTGGGAGGATTGTT AGTTGGGCATGGTTATGAGTGCTTGTAGTCCA_GCCACTTGGGAGGCTGAGGTGGGAGGATTGTT CT C GUSB Ensembl:ENSG00000169919 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs939264941 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_91111,RMVar_hsa_circ_101593,RMVar_hsa_circ_85354,RMVar_hsa_circ_245298,RMVar_hsa_circ_245299,RMVar_hsa_circ_245297,RMVar_hsa_circ_68586,RMVar_hsa_circ_329284,RMVar_hsa_circ_348911,RMVar_hsa_circ_363792,RMVar_hsa_circ_270006,RMVar_hsa_circ_245301,RMVar_hsa_circ_245302,RMVar_hsa_circ_245300 30394 RMVar_ID_30394 Human_SNP_ID_324105321 A-to-I Human chr7 - 65967909 65967909 65967909 GAGTGCTGAACGGGCTCTGCTGCTCTGGTCCTAGGCTCCGTATGTGGATGTGATCTGTTTGAACA GAGTGCTGAACGGGCTCTGCTGCTCTGGTCCTGGGCTCCGTATGTGGATGTGATCTGTTTGAACA T C GUSB Ensembl:ENSG00000169919 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1260794203 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_954462,Human_RBP_ID_16193646,Human_RBP_ID_24221576 RMVar_hsa_circ_47005,RMVar_hsa_circ_91111,RMVar_hsa_circ_101593,RMVar_hsa_circ_245298,RMVar_hsa_circ_245299,RMVar_hsa_circ_68586,RMVar_hsa_circ_329284,RMVar_hsa_circ_348911,RMVar_hsa_circ_363792,RMVar_hsa_circ_245301,RMVar_hsa_circ_245302,RMVar_hsa_circ_362431,RMVar_hsa_circ_245303 30395 RMVar_ID_30395 Human_SNP_ID_324105322 A-to-I Human chr7 - 65967909 65967909 65967909 GAGTGCTGAACGGGCTCTGCTGCTCTGGTCCTAGGCTCCGTATGTGGATGTGATCTGTTTGAACA GAGTGCTGAACGGGCTCTGCTGCTCTGGTCCTCGGCTCCGTATGTGGATGTGATCTGTTTGAACA T G GUSB Ensembl:ENSG00000169919 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1260794203 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_954462,Human_RBP_ID_16193646,Human_RBP_ID_24221576 RMVar_hsa_circ_47005,RMVar_hsa_circ_91111,RMVar_hsa_circ_101593,RMVar_hsa_circ_245298,RMVar_hsa_circ_245299,RMVar_hsa_circ_68586,RMVar_hsa_circ_329284,RMVar_hsa_circ_348911,RMVar_hsa_circ_363792,RMVar_hsa_circ_245301,RMVar_hsa_circ_245302,RMVar_hsa_circ_362431,RMVar_hsa_circ_245303 30396 RMVar_ID_30396 Human_SNP_ID_324105578 A-to-I Human chr7 - 65968862 65968862 65968862 TCTGTGACAGCCGGGCATGGTGGCTTACACCTATCATCCCAGCACTTTGGGAGGCCGAGGCAGGC TCTGTGACAGCCGGGCATGGTGGCTTACACCTGTCATCCCAGCACTTTGGGAGGCCGAGGCAGGC T C GUSB Ensembl:ENSG00000169919 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1231292611 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16193666 RMVar_hsa_circ_47005,RMVar_hsa_circ_91111,RMVar_hsa_circ_101593,RMVar_hsa_circ_245298,RMVar_hsa_circ_245299,RMVar_hsa_circ_68586,RMVar_hsa_circ_329284,RMVar_hsa_circ_348911,RMVar_hsa_circ_363792,RMVar_hsa_circ_245301,RMVar_hsa_circ_245302,RMVar_hsa_circ_362431,RMVar_hsa_circ_245303 30397 RMVar_ID_30397 Human_SNP_ID_324105703 A-to-I Human chr7 - 65969370 65969370 65969370 TTTATTTATTTATTTATTTATTTTGAGATGGAATCTTGCTCTGTTGCCCAGGCTTGAGTGAAATG TTTATTTATTTATTTATTTATTTTGAGATGGACTCTTGCTCTGTTGCCCAGGCTTGAGTGAAATG T G GUSB Ensembl:ENSG00000169919 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054378292 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47005,RMVar_hsa_circ_91111,RMVar_hsa_circ_101593,RMVar_hsa_circ_245298,RMVar_hsa_circ_245299,RMVar_hsa_circ_68586,RMVar_hsa_circ_329284,RMVar_hsa_circ_348911,RMVar_hsa_circ_363792,RMVar_hsa_circ_245301,RMVar_hsa_circ_245302,RMVar_hsa_circ_362431,RMVar_hsa_circ_245303 30398 RMVar_ID_30398 Human_SNP_ID_324106757 A-to-I Human chr7 - 65973504 65973504 65973504 CGTCTCACTGCAACCTTCACCTTCCAGGTTCAAGTGATTCTCCTGCCTCAGCCTCCTGAGGAGTT CGTCTCACTGCAACCTTCACCTTCCAGGTTCAGGTGATTCTCCTGCCTCAGCCTCCTGAGGAGTT T C GUSB Ensembl:ENSG00000169919 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs574479106 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47005,RMVar_hsa_circ_91111,RMVar_hsa_circ_101593,RMVar_hsa_circ_245298,RMVar_hsa_circ_245299,RMVar_hsa_circ_68586,RMVar_hsa_circ_348911,RMVar_hsa_circ_363792,RMVar_hsa_circ_245302,RMVar_hsa_circ_85572,RMVar_hsa_circ_245304 30399 RMVar_ID_30399 Human_SNP_ID_324107304 A-to-I Human chr7 - 65975025 65975025 65975025 ACAGACGTCACTGGGGCCTGTGTCTGACTTCTACACACTCCCTGTGGGGATCCGCACTGTGGCTG ACAGACGTCACTGGGGCCTGTGTCTGACTTCTCCACACTCCCTGTGGGGATCCGCACTGTGGCTG T G GUSB Ensembl:ENSG00000169919 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs886044680 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_870518,Human_Splice_Rec_870544,Human_Splice_Rec_870562,Human_Splice_Rec_870580,Human_Splice_Rec_870628 Human_miRNA_ID_658816,Human_miRNA_ID_1960385,Human_miRNA_ID_1983344,Human_miRNA_ID_2910041 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_329280,RMVar_hsa_circ_119821,RMVar_hsa_circ_280932,RMVar_hsa_circ_245310,RMVar_hsa_circ_245309,RMVar_hsa_circ_245307,RMVar_hsa_circ_245311 30400 RMVar_ID_30400 Human_SNP_ID_324107428 A-to-I Human chr7 - 65975500 65975500 65975500 AACACCTGTAATTCCAGCCACTCGGGAGGCTGAGGCAGGAGAATTGCTTGAACTCAGGAGGCAGA AACACCTGTAATTCCAGCCACTCGGGAGGCTGGGGCAGGAGAATTGCTTGAACTCAGGAGGCAGA T C GUSB Ensembl:ENSG00000169919 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs894160931 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 30401 RMVar_ID_30401 Human_SNP_ID_324107449 A-to-I Human chr7 - 65975657 65975657 65975657 TTGTAGCCTGGGCAGAGTGACTCATGCCTGTAATCTCAGCATTTTGGGAGGCTGAGGTGGGTGGA TTGTAGCCTGGGCAGAGTGACTCATGCCTGTACTCTCAGCATTTTGGGAGGCTGAGGTGGGTGGA T G GUSB Ensembl:ENSG00000169919 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-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 30402 RMVar_ID_30402 Human_SNP_ID_324107477 A-to-I Human chr7 - 65975812 65975812 65975812 TGGTCTCACTCTGTCACCCAGGCTGGAGTGCAATGGCCTGATCACAGCTCACTGCAGCCTTGAAC TGGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGCCTGATCACAGCTCACTGCAGCCTTGAAC T C GUSB Ensembl:ENSG00000169919 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs564495475 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 30403 RMVar_ID_30403 Human_SNP_ID_324107987 A-to-I Human chr7 - 65977333 65977333 65977333 GTTCAAACCAGCTTAGCCAACATTAGCTGGACATTGTGGTGTGAGCCTGCAATCCCGGCTACTCA GTTCAAACCAGCTTAGCCAACATTAGCTGGACGTTGTGGTGTGAGCCTGCAATCCCGGCTACTCA T C GUSB Ensembl:ENSG00000169919 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1488239561 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19148,RMVar_hsa_circ_91111,RMVar_hsa_circ_245299,RMVar_hsa_circ_68586,RMVar_hsa_circ_109676,RMVar_hsa_circ_285501,RMVar_hsa_circ_119821,RMVar_hsa_circ_245310,RMVar_hsa_circ_245309,RMVar_hsa_circ_77148,RMVar_hsa_circ_245311,RMVar_hsa_circ_338484,RMVar_hsa_circ_66026,RMVar_hsa_circ_245313 30404 RMVar_ID_30404 Human_SNP_ID_324108211 A-to-I Human chr7 - 65978061 65978061 65978061 TCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGGGGATCACGAGGTCAGGAGATCGCG TCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGGGGATCACGAGGTCAGGAGATCGCG T C GUSB Ensembl:ENSG00000169919 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs766989872 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19148,RMVar_hsa_circ_91111,RMVar_hsa_circ_245299,RMVar_hsa_circ_68586,RMVar_hsa_circ_109676,RMVar_hsa_circ_285501,RMVar_hsa_circ_119821,RMVar_hsa_circ_245310,RMVar_hsa_circ_245309,RMVar_hsa_circ_77148,RMVar_hsa_circ_245311,RMVar_hsa_circ_338484,RMVar_hsa_circ_66026,RMVar_hsa_circ_245313 30405 RMVar_ID_30405 Human_SNP_ID_324108302 A-to-I Human chr7 - 65978361 65978361 65978361 TCACTGCAACCTCCGCCTCCCGGGTTCAAACAATTCTCTTGCCTCAGCCTCCTGAGCAGCTGGGA TCACTGCAACCTCCGCCTCCCGGGTTCAAACAGTTCTCTTGCCTCAGCCTCCTGAGCAGCTGGGA T C GUSB Ensembl:ENSG00000169919 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1242705497 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19148,RMVar_hsa_circ_91111,RMVar_hsa_circ_245299,RMVar_hsa_circ_68586,RMVar_hsa_circ_109676,RMVar_hsa_circ_285501,RMVar_hsa_circ_119821,RMVar_hsa_circ_245310,RMVar_hsa_circ_245309,RMVar_hsa_circ_77148,RMVar_hsa_circ_245311,RMVar_hsa_circ_338484,RMVar_hsa_circ_66026,RMVar_hsa_circ_245313 30406 RMVar_ID_30406 Human_SNP_ID_324108375 A-to-I Human chr7 - 65978557 65978557 65978557 CACTCTATTGGCCTGACTGGTCTTGAACTCCTAACCTCAGGTGATCCACCCTCCTCGGCCTGCCA CACTCTATTGGCCTGACTGGTCTTGAACTCCTCACCTCAGGTGATCCACCCTCCTCGGCCTGCCA T G GUSB Ensembl:ENSG00000169919 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs867714919 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16193881 RMVar_hsa_circ_19148,RMVar_hsa_circ_91111,RMVar_hsa_circ_245299,RMVar_hsa_circ_68586,RMVar_hsa_circ_109676,RMVar_hsa_circ_285501,RMVar_hsa_circ_119821,RMVar_hsa_circ_245310,RMVar_hsa_circ_245309,RMVar_hsa_circ_77148,RMVar_hsa_circ_245311,RMVar_hsa_circ_338484,RMVar_hsa_circ_66026,RMVar_hsa_circ_245313 30407 RMVar_ID_30407 Human_SNP_ID_324108380 A-to-I Human chr7 - 65978583 65978583 65978583 ATTTTTTTTTAGTAGAGACAGGGTTTCACTCTATTGGCCTGACTGGTCTTGAACTCCTAACCTCA ATTTTTTTTTAGTAGAGACAGGGTTTCACTCTGTTGGCCTGACTGGTCTTGAACTCCTAACCTCA T C GUSB Ensembl:ENSG00000169919 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1215155131 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16193881 RMVar_hsa_circ_19148,RMVar_hsa_circ_91111,RMVar_hsa_circ_245299,RMVar_hsa_circ_68586,RMVar_hsa_circ_109676,RMVar_hsa_circ_285501,RMVar_hsa_circ_119821,RMVar_hsa_circ_245310,RMVar_hsa_circ_245309,RMVar_hsa_circ_77148,RMVar_hsa_circ_245311,RMVar_hsa_circ_338484,RMVar_hsa_circ_66026,RMVar_hsa_circ_245313 30408 RMVar_ID_30408 Human_SNP_ID_324108486 A-to-I Human chr7 - 65978933 65978933 65978933 GTGAGGCCATCACCACAAAAAATTAAAAAATTAGCCAGGGATGGTGATGTGTGCCGGTAGTCCCA GTGAGGCCATCACCACAAAAAATTAAAAAATTCGCCAGGGATGGTGATGTGTGCCGGTAGTCCCA T G GUSB Ensembl:ENSG00000169919 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1468307340 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19148,RMVar_hsa_circ_91111,RMVar_hsa_circ_245299,RMVar_hsa_circ_68586,RMVar_hsa_circ_109676,RMVar_hsa_circ_285501,RMVar_hsa_circ_119821,RMVar_hsa_circ_245310,RMVar_hsa_circ_245309,RMVar_hsa_circ_77148,RMVar_hsa_circ_245311,RMVar_hsa_circ_338484,RMVar_hsa_circ_66026,RMVar_hsa_circ_245313 30409 RMVar_ID_30409 Human_SNP_ID_324108487 A-to-I Human chr7 - 65978936 65978936 65978936 ATAGTGAGGCCATCACCACAAAAAATTAAAAAATTAGCCAGGGATGGTGATGTGTGCCGGTAGTC ATAGTGAGGCCATCACCACAAAAAATTAAAAATTTAGCCAGGGATGGTGATGTGTGCCGGTAGTC T A GUSB Ensembl:ENSG00000169919 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903007109 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19148,RMVar_hsa_circ_91111,RMVar_hsa_circ_245299,RMVar_hsa_circ_68586,RMVar_hsa_circ_109676,RMVar_hsa_circ_285501,RMVar_hsa_circ_119821,RMVar_hsa_circ_245310,RMVar_hsa_circ_245309,RMVar_hsa_circ_77148,RMVar_hsa_circ_245311,RMVar_hsa_circ_338484,RMVar_hsa_circ_66026,RMVar_hsa_circ_245313 30410 RMVar_ID_30410 Human_SNP_ID_324134104 A-to-I Human chr7 + 66079878 66079878 66079878 CTGACCTCATGATCCACCCACCTTAGCCTTCCAAAATGCTGGGATTACAGGCATGAGCCACCACT CTGACCTCATGATCCACCCACCTTAGCCTTCCGAAATGCTGGGATTACAGGCATGAGCCACCACT A G ASL Ensembl:ENSG00000126522 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs867937961 Functional Loss SNV dbSNP153 33..33 33 - - - 30411 RMVar_ID_30411 Human_SNP_ID_324134296 A-to-I Human chr7 + 66080503 66080503 66080503 CAAGCACTTCGGGATGCCAAGGTCAGGGGATCACCTGAGATCAGGAGTTCGAGACCAGCCTGACC CAAGCACTTCGGGATGCCAAGGTCAGGGGATCGCCTGAGATCAGGAGTTCGAGACCAGCCTGACC A G ASL Ensembl:ENSG00000126522 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1425992234 Functional Loss SNV dbSNP153 33..33 33 - - - 30412 RMVar_ID_30412 Human_SNP_ID_324134316 A-to-I Human chr7 + 66080564 66080564 66080564 GACCAACATGGTGAAACCCCGTCTCTACTAAAAATATAAAACTCAGCCAGGTGTGGTGGCACACG GACCAACATGGTGAAACCCCGTCTCTACTAAATATATAAAACTCAGCCAGGTGTGGTGGCACACG A T ASL Ensembl:ENSG00000126522 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1330664435 Functional Loss SNV dbSNP153 33..33 33 - - - 30413 RMVar_ID_30413 Human_SNP_ID_324134518 A-to-I Human chr7 + 66081418 66081418 66081418 CCTGGCCAACATGGTGAAACCCCATCTCTACTAATGATACAAAAATTAGCTGGGTGTGGTGGCAC CCTGGCCAACATGGTGAAACCCCATCTCTACTGATGATACAAAAATTAGCTGGGTGTGGTGGCAC A G ASL Ensembl:ENSG00000126522 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167809339 Functional Loss SNV dbSNP153 33..33 33 - - - 30414 RMVar_ID_30414 Human_SNP_ID_324135336 A-to-I Human chr7 + 66084299 66084299 66084299 CTAGTGCCTCAGCCTCCCAAGTAGCTGAGATTACAGGTGTGCACCACCATGTCCAGCTAATTTTT CTAGTGCCTCAGCCTCCCAAGTAGCTGAGATTGCAGGTGTGCACCACCATGTCCAGCTAATTTTT A G ASL Ensembl:ENSG00000126522 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1316246432 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33843,RMVar_hsa_circ_124968,RMVar_hsa_circ_57617,RMVar_hsa_circ_74436,RMVar_hsa_circ_245318,RMVar_hsa_circ_89383,RMVar_hsa_circ_245319,RMVar_hsa_circ_88651,RMVar_hsa_circ_245323,RMVar_hsa_circ_127628,RMVar_hsa_circ_245321,RMVar_hsa_circ_118242,RMVar_hsa_circ_245322 30415 RMVar_ID_30415 Human_SNP_ID_324135368 A-to-I Human chr7 + 66084430 66084430 66084430 GTGATCTGCCCGCGTCGGCCTGCCAAAGTGCTAGGATTACACCCATAAGCCACTGCGCTCAGCTT GTGATCTGCCCGCGTCGGCCTGCCAAAGTGCTGGGATTACACCCATAAGCCACTGCGCTCAGCTT A G ASL Ensembl:ENSG00000126522 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1379603496 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33843,RMVar_hsa_circ_124968,RMVar_hsa_circ_57617,RMVar_hsa_circ_74436,RMVar_hsa_circ_245318,RMVar_hsa_circ_89383,RMVar_hsa_circ_245319,RMVar_hsa_circ_88651,RMVar_hsa_circ_245323,RMVar_hsa_circ_127628,RMVar_hsa_circ_245321,RMVar_hsa_circ_118242,RMVar_hsa_circ_245322 30416 RMVar_ID_30416 Human_SNP_ID_324135712 A-to-I Human chr7 + 66085738 66085738 66085738 CATGCCATTCTCCTGCCTCAGCCCTCCTGAGTAGCTGGAACTACAGGCGCCCACCACTACGCCCG CATGCCATTCTCCTGCCTCAGCCCTCCTGAGTTGCTGGAACTACAGGCGCCCACCACTACGCCCG A T ASL Ensembl:ENSG00000126522 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1429877858 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33843,RMVar_hsa_circ_124968,RMVar_hsa_circ_57617,RMVar_hsa_circ_74436,RMVar_hsa_circ_245318,RMVar_hsa_circ_89383,RMVar_hsa_circ_245319,RMVar_hsa_circ_88651,RMVar_hsa_circ_245323,RMVar_hsa_circ_127628,RMVar_hsa_circ_245321,RMVar_hsa_circ_118242,RMVar_hsa_circ_245322 30417 RMVar_ID_30417 Human_SNP_ID_324135770 A-to-I Human chr7 + 66085941 66085941 66085941 CAAGACCCCATCTTTACAAAAAACTAAAAATTAGCTGGGCATGGTGGCATGTCCCTTTAGTCCCA CAAGACCCCATCTTTACAAAAAACTAAAAATTGGCTGGGCATGGTGGCATGTCCCTTTAGTCCCA A G ASL Ensembl:ENSG00000126522 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1408326124 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33843,RMVar_hsa_circ_124968,RMVar_hsa_circ_57617,RMVar_hsa_circ_74436,RMVar_hsa_circ_245318,RMVar_hsa_circ_89383,RMVar_hsa_circ_245319,RMVar_hsa_circ_88651,RMVar_hsa_circ_245323,RMVar_hsa_circ_127628,RMVar_hsa_circ_245321,RMVar_hsa_circ_118242,RMVar_hsa_circ_245322 30418 RMVar_ID_30418 Human_SNP_ID_324141167 A-to-I Human chr7 + 66102993 66102993 66102993 GCAGTGGCATGATCATAGCTCACTGTAACCTTAAACGCCTGGGCTCAAGTGATCCACCTCCCTCA GCAGTGGCATGATCATAGCTCACTGTAACCTTCAACGCCTGGGCTCAAGTGATCCACCTCCCTCA A C AC068533.4 Ensembl:ENSG00000249319 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1171978691 Functional Loss SNV dbSNP153 33..33 33 - - - 30419 RMVar_ID_30419 Human_SNP_ID_324141733 A-to-I Human chr7 + 66105232 66105232 66105232 ACAAAACATTAGCCGGTTGTTGGCACGTGCCTATAATCCCAGCTACTTGAGAGGCTGAGGCAGGA ACAAAACATTAGCCGGTTGTTGGCACGTGCCTGTAATCCCAGCTACTTGAGAGGCTGAGGCAGGA A G AC068533.4 Ensembl:ENSG00000249319 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334592049 Functional Loss SNV dbSNP153 33..33 33 - - - 30420 RMVar_ID_30420 Human_SNP_ID_324144634 A-to-I Human chr7 + 66116348 66116348 66116348 GAGACCCTGTCTCTGCAAAAAATTAAGAAGTTAGCTGGGTGTGGTGGTTCATGCCTGTAGTCTCA GAGACCCTGTCTCTGCAAAAAATTAAGAAGTTGGCTGGGTGTGGTGGTTCATGCCTGTAGTCTCA A G CRCP,AC068533.4 Ensembl:ENSG00000241258,Ensembl:ENSG00000249319 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs893441557 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23077485 RMVar_hsa_circ_245326,RMVar_hsa_circ_109892 30421 RMVar_ID_30421 Human_SNP_ID_324144792 A-to-I Human chr7 + 66116911 66116911 66116911 AGGAGGCCGAAGTGGGCGAATCCCCTGAGGTCAGGAGTTTGAGACCAGCCTGGCCAACATGGCAT AGGAGGCCGAAGTGGGCGAATCCCCTGAGGTCGGGAGTTTGAGACCAGCCTGGCCAACATGGCAT A G CRCP,AC068533.4 Ensembl:ENSG00000241258,Ensembl:ENSG00000249319 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1257510655 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_245326,RMVar_hsa_circ_109892 30422 RMVar_ID_30422 Human_SNP_ID_324148701 A-to-I Human chr7 + 66131136 66131136 66131136 AGCTGGGACTGCAGGCGCCCTCCACCACGGCCAGCTGATTTTTTGTATTTTTAGTAGAGACAGGG AGCTGGGACTGCAGGCGCCCTCCACCACGGCCTGCTGATTTTTTGTATTTTTAGTAGAGACAGGG A T CRCP,AC068533.4 Ensembl:ENSG00000241258,Ensembl:ENSG00000249319 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs545306660 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_245329,RMVar_hsa_circ_273218,RMVar_hsa_circ_245327,RMVar_hsa_circ_288431,RMVar_hsa_circ_245330,RMVar_hsa_circ_377584,RMVar_hsa_circ_245331,RMVar_hsa_circ_245333,RMVar_hsa_circ_75067,RMVar_hsa_circ_281532,RMVar_hsa_circ_302999,RMVar_hsa_circ_245334 30423 RMVar_ID_30423 Human_SNP_ID_324149249 A-to-I Human chr7 + 66133248 66133248 66133248 TCATTCTTGGCCGGGTGCGGTGTCTCATGCCTATAATCCCAGCACTTTCGGAGGCCGAGGCGGGT TCATTCTTGGCCGGGTGCGGTGTCTCATGCCTGTAATCCCAGCACTTTCGGAGGCCGAGGCGGGT A G CRCP,AC068533.4 Ensembl:ENSG00000241258,Ensembl:ENSG00000249319 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs113814877 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_245329,RMVar_hsa_circ_273218,RMVar_hsa_circ_245327,RMVar_hsa_circ_288431,RMVar_hsa_circ_245330,RMVar_hsa_circ_377584,RMVar_hsa_circ_245331,RMVar_hsa_circ_245333,RMVar_hsa_circ_75067,RMVar_hsa_circ_281532,RMVar_hsa_circ_302999,RMVar_hsa_circ_245334 30424 RMVar_ID_30424 Human_SNP_ID_324149477 A-to-I Human chr7 + 66133952 66133952 66133952 GTGATCTCGGCTCACTGCAACCTCTGCCTCCCAGGTTCAAGTGTTTCTCCTGCCTCAGCCTCCCT GTGATCTCGGCTCACTGCAACCTCTGCCTCCCCGGTTCAAGTGTTTCTCCTGCCTCAGCCTCCCT A C CRCP,AC068533.4 Ensembl:ENSG00000241258,Ensembl:ENSG00000249319 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2244226 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_245329,RMVar_hsa_circ_273218,RMVar_hsa_circ_245327,RMVar_hsa_circ_288431,RMVar_hsa_circ_245330,RMVar_hsa_circ_377584,RMVar_hsa_circ_245331,RMVar_hsa_circ_245333,RMVar_hsa_circ_75067,RMVar_hsa_circ_281532,RMVar_hsa_circ_302999,RMVar_hsa_circ_245334 30425 RMVar_ID_30425 Human_SNP_ID_324149478 A-to-I Human chr7 + 66133952 66133952 66133952 GTGATCTCGGCTCACTGCAACCTCTGCCTCCCAGGTTCAAGTGTTTCTCCTGCCTCAGCCTCCCT GTGATCTCGGCTCACTGCAACCTCTGCCTCCCGGGTTCAAGTGTTTCTCCTGCCTCAGCCTCCCT A G CRCP,AC068533.4 Ensembl:ENSG00000241258,Ensembl:ENSG00000249319 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2244226 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_245329,RMVar_hsa_circ_273218,RMVar_hsa_circ_245327,RMVar_hsa_circ_288431,RMVar_hsa_circ_245330,RMVar_hsa_circ_377584,RMVar_hsa_circ_245331,RMVar_hsa_circ_245333,RMVar_hsa_circ_75067,RMVar_hsa_circ_281532,RMVar_hsa_circ_302999,RMVar_hsa_circ_245334 30426 RMVar_ID_30426 Human_SNP_ID_324150110 A-to-I Human chr7 + 66136370 66136370 66136370 CTCCTGCCTCAGCCTCCACAGTAGCTGGGATTACAGGCATCTGCCACCACACCTGGCTAGTTTTG CTCCTGCCTCAGCCTCCACAGTAGCTGGGATTGCAGGCATCTGCCACCACACCTGGCTAGTTTTG A G CRCP,AC068533.4 Ensembl:ENSG00000241258,Ensembl:ENSG00000249319 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs755693214 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_273218,RMVar_hsa_circ_245330,RMVar_hsa_circ_302999,RMVar_hsa_circ_245334,RMVar_hsa_circ_245335 30427 RMVar_ID_30427 Human_SNP_ID_324150145 A-to-I Human chr7 + 66136504 66136504 66136504 CATCCACCTCGACCTCTCAAAGTTCTGGGATTACAGGTGTGAGTCACCGTGCCTGGCCAATTTTG CATCCACCTCGACCTCTCAAAGTTCTGGGATTTCAGGTGTGAGTCACCGTGCCTGGCCAATTTTG A T CRCP,AC068533.4 Ensembl:ENSG00000241258,Ensembl:ENSG00000249319 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1402021488 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_273218,RMVar_hsa_circ_245330,RMVar_hsa_circ_302999,RMVar_hsa_circ_245334,RMVar_hsa_circ_245335 30428 RMVar_ID_30428 Human_SNP_ID_324151641 A-to-I Human chr7 + 66142680 66142680 66142680 GCTTGGCTAATTGTTTTATTTTTATTTTTTGTAAAGACAGAGTCTCACTTTGTTGCCCAGGCTGT GCTTGGCTAATTGTTTTATTTTTATTTTTTGTGAAGACAGAGTCTCACTTTGTTGCCCAGGCTGT A G CRCP,AC068533.4 Ensembl:ENSG00000241258,Ensembl:ENSG00000249319 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049012005 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_273218,RMVar_hsa_circ_245330,RMVar_hsa_circ_302999,RMVar_hsa_circ_245334,RMVar_hsa_circ_245335 30429 RMVar_ID_30429 Human_SNP_ID_324152099 A-to-I Human chr7 + 66144920 66144920 66144920 GCCTATATCTTACCACTTTGGGAGGTCGAGGCAGGTGGATCCCCTGAGGTCGAGGGTTTGAGACC GCCTATATCTTACCACTTTGGGAGGTCGAGGCGGGTGGATCCCCTGAGGTCGAGGGTTTGAGACC A G CRCP,AC068533.4 Ensembl:ENSG00000241258,Ensembl:ENSG00000249319 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1159025037 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17577419 RMVar_hsa_circ_273218,RMVar_hsa_circ_245330,RMVar_hsa_circ_302999,RMVar_hsa_circ_245334,RMVar_hsa_circ_245335 30430 RMVar_ID_30430 Human_SNP_ID_324153327 A-to-I Human chr7 + 66150160 66150160 66150160 GTTTTTGGCCGGGCGCGGTGGCTAACTCCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGAGTGG GTTTTTGGCCGGGCGCGGTGGCTAACTCCTGTGATCCCAGCACTTTGGGAGGCCGAGGTGAGTGG A G CRCP,AC068533.4 Ensembl:ENSG00000241258,Ensembl:ENSG00000249319 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs552709347 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_103 30431 RMVar_ID_30431 Human_SNP_ID_324154238 A-to-I Human chr7 + 66153308 66153308 66153308 AAAAAAATACAAAATTAACCAGGGGTGATGGCACATTCCTGTAATCCCAGCTACTCGGGAGGCCG AAAAAAATACAAAATTAACCAGGGGTGATGGCCCATTCCTGTAATCCCAGCTACTCGGGAGGCCG A C CRCP Ensembl:ENSG00000241258 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1562776151 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26548176 Human_miRNA_ID_32454,Human_miRNA_ID_554321,Human_miRNA_ID_1333310 30432 RMVar_ID_30432 Human_SNP_ID_324154251 A-to-I Human chr7 + 66153345 66153345 66153345 CCTGTAATCCCAGCTACTCGGGAGGCCGAGGCAGGAGAATCGCTTGAACCCGGGAGGCAGAGGTT CCTGTAATCCCAGCTACTCGGGAGGCCGAGGCGGGAGAATCGCTTGAACCCGGGAGGCAGAGGTT A G CRCP Ensembl:ENSG00000241258 Protein coding 3'UTR GSE38233;GSE99789 cultured B-cells;esophageal squamous carcinoma cells,EC109 - 24183664,29796672 RNA-Seq:(High) rs1481119801 Functional Loss SNV dbSNP153 33..33 33 - - - 30433 RMVar_ID_30433 Human_SNP_ID_324154362 A-to-I Human chr7 + 66153875 66153875 66153875 GAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCCCCATCTCTACTAAAGATATAA GAGGTCAGGAGTTCAAGACCAGCCTGGCCAACGTGGTGAAACCCCCATCTCTACTAAAGATATAA A G CRCP Ensembl:ENSG00000241258 Protein coding 3'UTR GSE38233;GSE100210;GSE107867;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;ASD brains,cerebellum;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,30559470,32596459 RNA-Seq:(High) rs1255904448 Functional Loss SNV dbSNP153 33..33 33 - - - 30434 RMVar_ID_30434 Human_SNP_ID_324154363 A-to-I Human chr7 + 66153882 66153882 66153882 GGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCCCCATCTCTACTAAAGATATAAAAAACTA GGAGTTCAAGACCAGCCTGGCCAACATGGTGACACCCCCATCTCTACTAAAGATATAAAAAACTA A C CRCP Ensembl:ENSG00000241258 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1040906351 Functional Loss SNV dbSNP153 33..33 33 - - - 30435 RMVar_ID_30435 Human_SNP_ID_324154486 A-to-I Human chr7 + 66154250 66154250 66154250 TGCCCAGGAGTGCAGTGGCACGATCTCTGCTCACTGCAACCTCTGCCTCCCAGATTCAAGCGATT TGCCCAGGAGTGCAGTGGCACGATCTCTGCTCGCTGCAACCTCTGCCTCCCAGATTCAAGCGATT A G CRCP Ensembl:ENSG00000241258 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1129541 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26551345 30436 RMVar_ID_30436 Human_SNP_ID_324154488 A-to-I Human chr7 + 66154255 66154255 66154255 AGGAGTGCAGTGGCACGATCTCTGCTCACTGCAACCTCTGCCTCCCAGATTCAAGCGATTCTGGT AGGAGTGCAGTGGCACGATCTCTGCTCACTGCGACCTCTGCCTCCCAGATTCAAGCGATTCTGGT A G CRCP Ensembl:ENSG00000241258 Protein coding 3'UTR GSE38233;GSE100210;GSE100210;GSE107867;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,29129909,30559470,32596459 RNA-Seq:(High) rs1129542 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26551346 30437 RMVar_ID_30437 Human_SNP_ID_324154498 A-to-I Human chr7 + 66154305 66154305 66154305 TCAAGCGATTCTGGTGCCTTAGCCTCCTGAGTAGCTGGGACTTACAGGCACGTACCACTATACCC TCAAGCGATTCTGGTGCCTTAGCCTCCTGAGTGGCTGGGACTTACAGGCACGTACCACTATACCC A G CRCP Ensembl:ENSG00000241258 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1129546 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22372355,Human_RBP_ID_26550534 30438 RMVar_ID_30438 Human_SNP_ID_324154507 A-to-I Human chr7 + 66154342 66154342 66154342 GGACTTACAGGCACGTACCACTATACCCTGCTAAAATTTGTATTTTTAGTAGAGACAGGGTTTTG GGACTTACAGGCACGTACCACTATACCCTGCTGAAATTTGTATTTTTAGTAGAGACAGGGTTTTG A G CRCP Ensembl:ENSG00000241258 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1373308851 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8669965,Human_RBP_ID_26550534 30439 RMVar_ID_30439 Human_SNP_ID_324154511 A-to-I Human chr7 + 66154357 66154357 66154357 TACCACTATACCCTGCTAAAATTTGTATTTTTAGTAGAGACAGGGTTTTGCCATATTGGCCAGGC TACCACTATACCCTGCTAAAATTTGTATTTTTGGTAGAGACAGGGTTTTGCCATATTGGCCAGGC A G CRCP Ensembl:ENSG00000241258 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1129529 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26110853,Human_RBP_ID_26550535 30440 RMVar_ID_30440 Human_SNP_ID_324154514 A-to-I Human chr7 + 66154360 66154360 66154360 CACTATACCCTGCTAAAATTTGTATTTTTAGTAGAGACAGGGTTTTGCCATATTGGCCAGGCTAG CACTATACCCTGCTAAAATTTGTATTTTTAGTGGAGACAGGGTTTTGCCATATTGGCCAGGCTAG A G CRCP Ensembl:ENSG00000241258 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1129547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26550535 30441 RMVar_ID_30441 Human_SNP_ID_324154520 A-to-I Human chr7 + 66154379 66154379 66154379 TTGTATTTTTAGTAGAGACAGGGTTTTGCCATATTGGCCAGGCTAGTCGTAATGTCTCTTTTTAA TTGTATTTTTAGTAGAGACAGGGTTTTGCCATGTTGGCCAGGCTAGTCGTAATGTCTCTTTTTAA A G CRCP Ensembl:ENSG00000241258 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1047476 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23198226,Human_RBP_ID_26550535 30442 RMVar_ID_30442 Human_SNP_ID_324154649 A-to-I Human chr7 + 66154801 66154801 66154801 TTTAGTAGAGACAGGGTTTCACCGTGTTAGCCAGGATGGTCTCAATCTCCTGACCTTGCCCACCT TTTAGTAGAGACAGGGTTTCACCGTGTTAGCCGGGATGGTCTCAATCTCCTGACCTTGCCCACCT A G lnc-VKORC1L1-2 RNACentral:URS00008BDB22 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs758153078 Functional Loss SNV dbSNP153 33..33 33 - - - 30443 RMVar_ID_30443 Human_SNP_ID_324154700 A-to-I Human chr7 + 66155066 66155066 66155066 AATAATAAATGTTTCAGAAATAAAAATTGGCCAGGCTCAGTGGCTCACGCCTGTAATCCCAGCAC AATAATAAATGTTTCAGAAATAAAAATTGGCCGGGCTCAGTGGCTCACGCCTGTAATCCCAGCAC A G lnc-VKORC1L1-2 RNACentral:URS00008BDB22 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs936705924 Functional Loss SNV dbSNP153 33..33 33 - - - 30444 RMVar_ID_30444 Human_SNP_ID_324154733 A-to-I Human chr7 + 66155230 66155230 66155230 TGGGTGTGGTGGCAGGCAACTGTATCCCAGCTACTTGGGAGGTTGAGGCAGGAGAATTGCTTGAA TGGGTGTGGTGGCAGGCAACTGTATCCCAGCTGCTTGGGAGGTTGAGGCAGGAGAATTGCTTGAA A G lnc-VKORC1L1-2 RNACentral:URS00008BDB22 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1392776334 Functional Loss SNV dbSNP153 33..33 33 - - - 30445 RMVar_ID_30445 Human_SNP_ID_324154756 A-to-I Human chr7 + 66155320 66155320 66155320 CTGAGATCGTGCCACTGTACTCCAGCCTGGGTAACAGAGTGAGACTCTGTCTCAAAAAAAAAATA CTGAGATCGTGCCACTGTACTCCAGCCTGGGTGACAGAGTGAGACTCTGTCTCAAAAAAAAAATA A G lnc-VKORC1L1-2 RNACentral:URS00008BDB22 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1350010364 Functional Loss SNV dbSNP153 33..33 33 - - - 30446 RMVar_ID_30446 Human_SNP_ID_324154874 A-to-I Human chr7 + 66155699 66155699 66155699 GGGACCACAGGTGTGTGCCACCACACCAGGCTAATTTTTTTGTATTTTTTTGTAGAGACGGGGTT GGGACCACAGGTGTGTGCCACCACACCAGGCTCATTTTTTTGTATTTTTTTGTAGAGACGGGGTT A C lnc-VKORC1L1-2 RNACentral:URS00008BDB22 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1490446136 Functional Loss SNV dbSNP153 33..33 33 - - - 30447 RMVar_ID_30447 Human_SNP_ID_324154875 A-to-I Human chr7 + 66155699 66155699 66155699 GGGACCACAGGTGTGTGCCACCACACCAGGCTAATTTTTTTGTATTTTTTTGTAGAGACGGGGTT GGGACCACAGGTGTGTGCCACCACACCAGGCTGATTTTTTTGTATTTTTTTGTAGAGACGGGGTT A G lnc-VKORC1L1-2 RNACentral:URS00008BDB22 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1490446136 Functional Loss SNV dbSNP153 33..33 33 - - - 30448 RMVar_ID_30448 Human_SNP_ID_324154901 A-to-I Human chr7 + 66155811 66155811 66155811 CGCTTGCCTTAGCCACCCAAAGTGCTGGAATTACATGGGTGAGCTACCGTGTCCAGCCTCAATTT CGCTTGCCTTAGCCACCCAAAGTGCTGGAATTGCATGGGTGAGCTACCGTGTCCAGCCTCAATTT A G lnc-VKORC1L1-2 RNACentral:URS00008BDB22 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1485107185 Functional Loss SNV dbSNP153 33..33 33 - - - 30449 RMVar_ID_30449 Human_SNP_ID_324154990 A-to-I Human chr7 + 66156194 66156194 66156194 CCAGCTACTCAGAAGGCTGAGGCAGGAGAGTCACTTGAACCCAGGTGGCAGAGGTTGCAGTGAGT CCAGCTACTCAGAAGGCTGAGGCAGGAGAGTCGCTTGAACCCAGGTGGCAGAGGTTGCAGTGAGT A G lnc-VKORC1L1-2,piR-41406 RNACentral:URS00008BDB22,RNACentral:URS00001034C4 lincRNA,piRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1347156552 Functional Loss SNV dbSNP153 33..33 33 - - - 30450 RMVar_ID_30450 Human_SNP_ID_324155342 A-to-I Human chr7 + 66157631 66157631 66157631 CAGCCTGGTCAGCATGGTGAAACCCTGTCTCTACAAAAATACCAAAACTAGCCAGATGCAGTGGT CAGCCTGGTCAGCATGGTGAAACCCTGTCTCTTCAAAAATACCAAAACTAGCCAGATGCAGTGGT A T lnc-VKORC1L1-2 RNACentral:URS00008BDB22 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1483694791 Functional Loss SNV dbSNP153 33..33 33 - - - 30451 RMVar_ID_30451 Human_SNP_ID_324155428 A-to-I Human chr7 + 66158104 66158104 66158104 ACCTCAAATGATCCCCCTGCCTCAGCCTCCCAAAGTGCTCCCAAAGTTACAGGCGTGAGCCACCT ACCTCAAATGATCCCCCTGCCTCAGCCTCCCAGAGTGCTCCCAAAGTTACAGGCGTGAGCCACCT A G lnc-VKORC1L1-2 RNACentral:URS00008BDB22 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs567934842 Functional Loss SNV dbSNP153 33..33 33 - - - 30452 RMVar_ID_30452 Human_SNP_ID_324155848 A-to-I Human chr7 + 66159828 66159828 66159828 TCATGCCTGTAATGCCAGCACTTTGGGAGACTAAGGCAGGCAGGTCACCTGAGGTCAGCAGTTCA TCATGCCTGTAATGCCAGCACTTTGGGAGACTGAGGCAGGCAGGTCACCTGAGGTCAGCAGTTCA A G lnc-VKORC1L1-2 RNACentral:URS00008BDB22 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1278641725 Functional Loss SNV dbSNP153 33..33 33 - - - 30453 RMVar_ID_30453 Human_SNP_ID_324183077 A-to-I Human chr7 + 66275604 66275604 66275604 CATCGTTAATAAACCTGTAGAACATTATTGTAAATGAAATAAGCCAGGCATGGAAAGACAAATAC CATCGTTAATAAACCTGTAGAACATTATTGTAGATGAAATAAGCCAGGCATGGAAAGACAAATAC A G TPST1 Ensembl:ENSG00000169902 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1181365880 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1240,RMVar_hsa_circ_105457,RMVar_hsa_circ_285863,RMVar_hsa_circ_245336,RMVar_hsa_circ_322796,RMVar_hsa_circ_245339 30454 RMVar_ID_30454 Human_SNP_ID_324190647 A-to-I Human chr7 + 66313364 66313364 66313364 TTGAACTCGGGAGGCGGAGGTTGCAGTGAGCCAAGATCATGCCATAACTCTCCAGCTTGGGTGAC TTGAACTCGGGAGGCGGAGGTTGCAGTGAGCCCAGATCATGCCATAACTCTCCAGCTTGGGTGAC A C TPST1 Ensembl:ENSG00000169902 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs767188030 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1240,RMVar_hsa_circ_322796,RMVar_hsa_circ_307103,RMVar_hsa_circ_317868,RMVar_hsa_circ_245343,RMVar_hsa_circ_245342 30455 RMVar_ID_30455 Human_SNP_ID_324191668 A-to-I Human chr7 + 66318012 66318012 66318012 GAAACCCCGTCTCTACTAAAAATATAAAAATTAGCCAGGCGGGGTGGCAGGCGCCTATAATCACA GAAACCCCGTCTCTACTAAAAATATAAAAATTGGCCAGGCGGGGTGGCAGGCGCCTATAATCACA A G TPST1 Ensembl:ENSG00000169902 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1158178680 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1240,RMVar_hsa_circ_322796,RMVar_hsa_circ_307103,RMVar_hsa_circ_317868,RMVar_hsa_circ_245343,RMVar_hsa_circ_245342 30456 RMVar_ID_30456 Human_SNP_ID_324192715 A-to-I Human chr7 + 66322666 66322666 66322666 TGATCAATTTGGGTTGCTTCCATTTCTTGGCTATTGTGAATAGTGCTGCAGTGAACATGATGTGC TGATCAATTTGGGTTGCTTCCATTTCTTGGCTGTTGTGAATAGTGCTGCAGTGAACATGATGTGC A G TPST1 Ensembl:ENSG00000169902 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978292741 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1240,RMVar_hsa_circ_322796,RMVar_hsa_circ_307103,RMVar_hsa_circ_317868,RMVar_hsa_circ_245343,RMVar_hsa_circ_245342 30457 RMVar_ID_30457 Human_SNP_ID_324193457 A-to-I Human chr7 + 66325781 66325781 66325781 CCTAAGCCTCCCAAGTAGCTGGGATTACAGGCACCCGCCTCCATGCCTGGCTAATTTTTGTATTT CCTAAGCCTCCCAAGTAGCTGGGATTACAGGCCCCCGCCTCCATGCCTGGCTAATTTTTGTATTT A C TPST1 Ensembl:ENSG00000169902 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1379138055 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1240,RMVar_hsa_circ_322796,RMVar_hsa_circ_307103,RMVar_hsa_circ_317868,RMVar_hsa_circ_245343,RMVar_hsa_circ_245342 30458 RMVar_ID_30458 Human_SNP_ID_324207570 A-to-I Human chr7 - 66380424 66380424 66380424 CTTCAGCTTCCCGAGTAGCTGGGATTATGAGTATGCACCACCACACGCAGCTAATTTTTTTCTTT CTTCAGCTTCCCGAGTAGCTGGGATTATGAGTGTGCACCACCACACGCAGCTAATTTTTTTCTTT T C LINC00174 Ensembl:ENSG00000179406 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1250673346 Functional Loss SNV dbSNP153 33..33 33 - - - 30459 RMVar_ID_30459 Human_SNP_ID_324207595 A-to-I Human chr7 - 66380546 66380546 66380546 TGTGTGTAAATAGTTGTTTTGTTCTTTGAGACAGGGTCTTGCTTTGTCACCCAGGCTTGACTATA TGTGTGTAAATAGTTGTTTTGTTCTTTGAGACGGGGTCTTGCTTTGTCACCCAGGCTTGACTATA T C LINC00174 Ensembl:ENSG00000179406 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1394021041 Functional Loss SNV dbSNP153 33..33 33 - - - 30460 RMVar_ID_30460 Human_SNP_ID_324208822 A-to-I Human chr7 - 66384897 66384895 66384898 GAGCTGAGGCAGGAAGATGGCTTAAATTCAGAAGGTCGAGGCTTCAGTGAGCTATAAGTGCACAA GAGCTGAGGCAGGAAGATGGCTTAAATTCAG___GTCGAGGCTTCAGTGAGCTATAAGTGCACAA CCTT C LINC00174 Ensembl:ENSG00000179406 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs948612423 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_245347,RMVar_hsa_circ_290314,RMVar_hsa_circ_245348 30461 RMVar_ID_30461 Human_SNP_ID_324209287 A-to-I Human chr7 - 66386970 66386970 66386970 TTTAGTAGAGACGAGGTCTCTCCCTGTTGGTCAGGCTGGTCTCAAACTCTTGACCTTAGGTGAAT TTTAGTAGAGACGAGGTCTCTCCCTGTTGGTCGGGCTGGTCTCAAACTCTTGACCTTAGGTGAAT T C LINC00174 Ensembl:ENSG00000179406 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1336371780 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_245347,RMVar_hsa_circ_290314,RMVar_hsa_circ_245348 30462 RMVar_ID_30462 Human_SNP_ID_324209315 A-to-I Human chr7 - 66387079 66387079 66387079 CGGCTCACCAAAACCTCCACCTCCTGGCTTCAAGCGATTCTCCTGCCTCAGCCTCCAGAGTAGCT CGGCTCACCAAAACCTCCACCTCCTGGCTTCAGGCGATTCTCCTGCCTCAGCCTCCAGAGTAGCT T C LINC00174 Ensembl:ENSG00000179406 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170061850 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_245347,RMVar_hsa_circ_290314,RMVar_hsa_circ_245348 30463 RMVar_ID_30463 Human_SNP_ID_324209374 A-to-I Human chr7 - 66387284 66387284 66387284 TGAGGTCTCACTATGTTGTCCCGGCTGGTTTCAAACTCTGGGCCTCAAGTGTTCCTCCTGCTTTG TGAGGTCTCACTATGTTGTCCCGGCTGGTTTCCAACTCTGGGCCTCAAGTGTTCCTCCTGCTTTG T G LINC00174 Ensembl:ENSG00000179406 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1301564929 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23198240 RMVar_hsa_circ_245347,RMVar_hsa_circ_290314,RMVar_hsa_circ_245348 30464 RMVar_ID_30464 Human_SNP_ID_324209874 A-to-I Human chr7 - 66389187 66389185 66389187 AAAACAGTTTGTTTCCTTTTTTTCTGAGAGACAGGGTCTCATTTTGTTGTCCAGGCTGGTGTGCA AAAACAGTTTGTTTCCTTTTTTTCTGAGAGAC__GGTCTCATTTTGTTGTCCAGGCTGGTGTGCA CCT C LINC00174 Ensembl:ENSG00000179406 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1464547705 Functional Loss DEL dbSNP153 33..34 33 - - - Human_Splice_Rec_871225 RMVar_hsa_circ_245347,RMVar_hsa_circ_290314,RMVar_hsa_circ_245348 30465 RMVar_ID_30465 Human_SNP_ID_324210542 A-to-I Human chr7 - 66391947 66391947 66391947 CTCCTTCCTCAGCCTCCCGAGTAGCTGGGATTACAGATATGTGCCACCACCCCTGGCTAATTTTT CTCCTTCCTCAGCCTCCCGAGTAGCTGGGATTGCAGATATGTGCCACCACCCCTGGCTAATTTTT T C LINC00174 Ensembl:ENSG00000179406 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1266156600 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_245347,RMVar_hsa_circ_290314,RMVar_hsa_circ_245348 30466 RMVar_ID_30466 Human_SNP_ID_324235311 A-to-I Human chr7 - 66491394 66491394 66491394 CTTGAAGTAATCTGCCCACCTCGGCTTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCGCC CTTGAAGTAATCTGCCCACCTCGGCTTCCCAAGGTGCTGGGATTACAGGCGTGAGCCACTGCGCC T C LINC00174 Ensembl:ENSG00000179406 lincRNA exon GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs923650321 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_871274,Human_Splice_Rec_871298,Human_Splice_Rec_871299 RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354 30467 RMVar_ID_30467 Human_SNP_ID_324235317 A-to-I Human chr7 - 66491418 66491418 66491418 GCCAGGCTGGTCTGGAACTCCTGACTTGAAGTAATCTGCCCACCTCGGCTTCCCAAAGTGCTGGG GCCAGGCTGGTCTGGAACTCCTGACTTGAAGTCATCTGCCCACCTCGGCTTCCCAAAGTGCTGGG T G LINC00174 Ensembl:ENSG00000179406 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1489854780 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_871274,Human_Splice_Rec_871298,Human_Splice_Rec_871299 RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354 30468 RMVar_ID_30468 Human_SNP_ID_324235352 A-to-I Human chr7 - 66491547 66491547 66491547 TTCACCCCCTCCCCCGCCCCCTGCCGGGTTCAAGTGATTCCCATGTTTCAGCTTCCTGAGTAGCT TTCACCCCCTCCCCCGCCCCCTGCCGGGTTCAGGTGATTCCCATGTTTCAGCTTCCTGAGTAGCT T C LINC00174 Ensembl:ENSG00000179406 lincRNA exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1408092877 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17577420 RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354 30469 RMVar_ID_30469 Human_SNP_ID_324235526 A-to-I Human chr7 - 66492081 66492081 66492081 ACTTTGGGAGGCTGAGACAGGTGGATCACTTGAGGCCAGGAGTTCGAGTCCCGCCTGGGCAACAT ACTTTGGGAGGCTGAGACAGGTGGATCACTTGGGGCCAGGAGTTCGAGTCCCGCCTGGGCAACAT T C LINC00174 Ensembl:ENSG00000179406 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1345533401 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18884701 RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354 30470 RMVar_ID_30470 Human_SNP_ID_324242228 A-to-I Human chr7 - 66517149 66517149 66517149 CGATTGACCGGGCGCAGTGGCTCATGCCTGTAATCTCAGCACTTTGGGAGGCCGAGGTGAGCGGA CGATTGACCGGGCGCAGTGGCTCATGCCTGTACTCTCAGCACTTTGGGAGGCCGAGGTGAGCGGA T G RF00017-4513 RNACentral:URS000090EECB SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1292787583 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354 30471 RMVar_ID_30471 Human_SNP_ID_324244677 A-to-I Human chr7 - 66526644 66526644 66526644 TCGGCTCACTGCAACCTCCGACTTCCAGTTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGC TCGGCTCACTGCAACCTCCGACTTCCAGTTTCCAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGC T G AC006001.3 Ensembl:ENSG00000229180 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs953675084 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354 30472 RMVar_ID_30472 Human_SNP_ID_324244683 A-to-I Human chr7 - 66526682 66526682 66526682 CACTCTTGTTGCCCAGGCTGGAGTGCAACGGCATGATCTCGGCTCACTGCAACCTCCGACTTCCA CACTCTTGTTGCCCAGGCTGGAGTGCAACGGCGTGATCTCGGCTCACTGCAACCTCCGACTTCCA T C AC006001.3 Ensembl:ENSG00000229180 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1280641524 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8273113,Human_RBP_ID_17430055 RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354 30473 RMVar_ID_30473 Human_SNP_ID_324244686 A-to-I Human chr7 - 66526687 66526687 66526687 AGTTTCACTCTTGTTGCCCAGGCTGGAGTGCAACGGCATGATCTCGGCTCACTGCAACCTCCGAC AGTTTCACTCTTGTTGCCCAGGCTGGAGTGCAGCGGCATGATCTCGGCTCACTGCAACCTCCGAC T C AC006001.3 Ensembl:ENSG00000229180 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1199914948 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8273113,Human_RBP_ID_17430055 RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354 30474 RMVar_ID_30474 Human_SNP_ID_324244870 A-to-I Human chr7 - 66527274 66527274 66527274 CGAATCACTTGAACTCGGGAGGTGGAGATCGCAGTGAGCCAAGATCGTGCCATTGCACTCCAGCC CGAATCACTTGAACTCGGGAGGTGGAGATCGCCGTGAGCCAAGATCGTGCCATTGCACTCCAGCC T G AC006001.3 Ensembl:ENSG00000229180 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1248985033 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17430058,Human_RBP_ID_18520347 RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354 30475 RMVar_ID_30475 Human_SNP_ID_324244879 A-to-I Human chr7 - 66527300 66527300 66527300 CCAGCTACTTGGGAGGCTGAGGCAGACGAATCACTTGAACTCGGGAGGTGGAGATCGCAGTGAGC CCAGCTACTTGGGAGGCTGAGGCAGACGAATCGCTTGAACTCGGGAGGTGGAGATCGCAGTGAGC T C AC006001.3 Ensembl:ENSG00000229180 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893348464 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17430058,Human_RBP_ID_18520347 Human_miRNA_ID_2015481 RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354 30476 RMVar_ID_30476 Human_SNP_ID_324244888 A-to-I Human chr7 - 66527336 66527336 66527336 AAAATTAGCCAGGTGTCGTGGTGCACACCCGTAATTCCAGCTACTTGGGAGGCTGAGGCAGACGA AAAATTAGCCAGGTGTCGTGGTGCACACCCGTGATTCCAGCTACTTGGGAGGCTGAGGCAGACGA T C AC006001.3 Ensembl:ENSG00000229180 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs555531022 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2085771 RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354 30477 RMVar_ID_30477 Human_SNP_ID_324244904 A-to-I Human chr7 - 66527414 66527414 66527414 GCGGGCTGATCACCTGAGGTCAGAAGTTTGAGATCAGCCTGGCCAACAGGGTGAAACCCTGTCTC GCGGGCTGATCACCTGAGGTCAGAAGTTTGAGGTCAGCCTGGCCAACAGGGTGAAACCCTGTCTC T C AC006001.3 Ensembl:ENSG00000229180 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1301427547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1950382,Human_miRNA_ID_1951665,Human_miRNA_ID_2516726 RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354 30478 RMVar_ID_30478 Human_SNP_ID_324245000 A-to-I Human chr7 - 66527809 66527809 66527809 CTTCCACCTCAGCCTCCCGAGTAGCTGGGAGTACAGGTGTTCGTCCCCACCATGTCTGGCTAATT CTTCCACCTCAGCCTCCCGAGTAGCTGGGAGTGCAGGTGTTCGTCCCCACCATGTCTGGCTAATT T C AC006001.3 Ensembl:ENSG00000229180 Pseudogene exon GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1200897448 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354 30479 RMVar_ID_30479 Human_SNP_ID_324245170 A-to-I Human chr7 - 66528500 66528500 66528500 TTTAGTAGAGTCGGGGTTTCACCATGTTGCCCAGGCTGGTCTCGAACTCCTGACCTTACGTGATC TTTAGTAGAGTCGGGGTTTCACCATGTTGCCCGGGCTGGTCTCGAACTCCTGACCTTACGTGATC T C AC006001.3 Ensembl:ENSG00000229180 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1441807543 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8272364,Human_RBP_ID_17427678,Human_RBP_ID_26111146 RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354 30480 RMVar_ID_30480 Human_SNP_ID_324245221 A-to-I Human chr7 - 66528645 66528644 66528645 CCTCTGTTGCCAGGCTGGAATGCCGTGGCGCAATCTCAGCTCACTGCAACCTCTACCTCCTGGGT CCTCTGTTGCCAGGCTGGAATGCCGTGGCGCA_TCTCAGCTCACTGCAACCTCTACCTCCTGGGT AT A AC006001.3 Ensembl:ENSG00000229180 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1198956361 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_19139816,Human_RBP_ID_21518986 RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354 30481 RMVar_ID_30481 Human_SNP_ID_324245222 A-to-I Human chr7 - 66528645 66528645 66528645 CCTCTGTTGCCAGGCTGGAATGCCGTGGCGCAATCTCAGCTCACTGCAACCTCTACCTCCTGGGT CCTCTGTTGCCAGGCTGGAATGCCGTGGCGCAGTCTCAGCTCACTGCAACCTCTACCTCCTGGGT T C AC006001.3 Ensembl:ENSG00000229180 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1489931803 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19139816,Human_RBP_ID_21518986 RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354 30482 RMVar_ID_30482 Human_SNP_ID_324245414 A-to-I Human chr7 - 66529377 66529377 66529377 TGTGGCTGGTCTCAAACTCCTGGGCTCAAGTGATCCTCCTGCCTCGGCCTCCCAAAGTGCTGGAT TGTGGCTGGTCTCAAACTCCTGGGCTCAAGTGTTCCTCCTGCCTCGGCCTCCCAAAGTGCTGGAT T A AC006001.3 Ensembl:ENSG00000229180 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335737751 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10369918,Human_RBP_ID_17430995 RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354 30483 RMVar_ID_30483 Human_SNP_ID_324245415 A-to-I Human chr7 - 66529381 66529381 66529381 GCTATGTGGCTGGTCTCAAACTCCTGGGCTCAAGTGATCCTCCTGCCTCGGCCTCCCAAAGTGCT GCTATGTGGCTGGTCTCAAACTCCTGGGCTCAGGTGATCCTCCTGCCTCGGCCTCCCAAAGTGCT T C AC006001.3 Ensembl:ENSG00000229180 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1180247808 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10369918,Human_RBP_ID_17430995 RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354 30484 RMVar_ID_30484 Human_SNP_ID_324246310 A-to-I Human chr7 - 66532528 66532528 66532528 AAACCCCGTCTCTACTAAAAATACAAAAAATTAGGTGGGCGAGGTGGTGCGCGCCTGTAGTCACA AAACCCCGTCTCTACTAAAAATACAAAAAATTGGGTGGGCGAGGTGGTGCGCGCCTGTAGTCACA T C AC006001.3 Ensembl:ENSG00000229180 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs976200253 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26111166 RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354 30485 RMVar_ID_30485 Human_SNP_ID_324246724 A-to-I Human chr7 - 66534140 66534140 66534140 TTTTGTGTTTTTAGTAGAGATGGGGTCTTGCCATGTTGCCCAGGCCGGTCTCAAATTCCTGAGCT TTTTGTGTTTTTAGTAGAGATGGGGTCTTGCCGTGTTGCCCAGGCCGGTCTCAAATTCCTGAGCT T C AC006001.3 Ensembl:ENSG00000229180 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1323402660 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17585888 RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354 30486 RMVar_ID_30486 Human_SNP_ID_324246885 A-to-I Human chr7 - 66534574 66534574 66534574 TTAGAGATGTAGACTCATTTTGTCACCCATGGAGTGGTGCGATCCTAGCTCACTGAAGCCTTGAC TTAGAGATGTAGACTCATTTTGTCACCCATGGTGTGGTGCGATCCTAGCTCACTGAAGCCTTGAC T A AC006001.3 Ensembl:ENSG00000229180 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1297315727 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_794177,Human_RBP_ID_3867662,Human_RBP_ID_16195476 RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354 30487 RMVar_ID_30487 Human_SNP_ID_324247472 A-to-I Human chr7 - 66536797 66536797 66536797 ACGCCTGTCATCCCAGCACTTTGTGGGGCTGAAGTGGGCATATCACCAGAGGTCAGGAGTTTAAG ACGCCTGTCATCCCAGCACTTTGTGGGGCTGAGGTGGGCATATCACCAGAGGTCAGGAGTTTAAG T C AC006001.3 Ensembl:ENSG00000229180 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs572714640 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16195535 RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354 30488 RMVar_ID_30488 Human_SNP_ID_324247616 A-to-I Human chr7 - 66537314 66537314 66537314 GTTGCCCAGGCTGATCTTCAACTCCTAAGCTCAAGCAATCCACCCATCTTGGCTTCCCAAAGTGC GTTGCCCAGGCTGATCTTCAACTCCTAAGCTCGAGCAATCCACCCATCTTGGCTTCCCAAAGTGC T C AC006001.3 Ensembl:ENSG00000229180 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs527451255 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354 30489 RMVar_ID_30489 Human_SNP_ID_324247653 A-to-I Human chr7 - 66537478 66537478 66537478 TTGCCCAGGCTGGAGTGCAGTGGAGCAATCTCAGCTCACTGTAACCTCCGCCTCCTGGACTGAAG TTGCCCAGGCTGGAGTGCAGTGGAGCAATCTCGGCTCACTGTAACCTCCGCCTCCTGGACTGAAG T C AC006001.3 Ensembl:ENSG00000229180 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1252829169 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354 30490 RMVar_ID_30490 Human_SNP_ID_324247804 A-to-I Human chr7 - 66538050 66538050 66538050 TCACATAGCAAAAAGCACTACAGGCTGGGCATAGTGGCTCATGTCTGTCATGCCAGCACTTTGGA TCACATAGCAAAAAGCACTACAGGCTGGGCATGGTGGCTCATGTCTGTCATGCCAGCACTTTGGA T C AC006001.3 Ensembl:ENSG00000229180 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559769852 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8273115 RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354 30491 RMVar_ID_30491 Human_SNP_ID_324248408 A-to-I Human chr7 - 66540317 66540317 66540317 ACTCAGGAGGCTGAGGCAGGAGAATCCCTTGAACTGGGAGGTGGAAGCTGCAGTGAGCTAAGATC ACTCAGGAGGCTGAGGCAGGAGAATCCCTTGAGCTGGGAGGTGGAAGCTGCAGTGAGCTAAGATC T C AC006001.3 Ensembl:ENSG00000229180 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1279026337 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_253972,Human_RBP_ID_16195634,Human_RBP_ID_17431010,Human_RBP_ID_18520521,Human_RBP_ID_21554248,Human_RBP_ID_22482988 RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354 30492 RMVar_ID_30492 Human_SNP_ID_324248526 A-to-I Human chr7 - 66540704 66540704 66540704 CGCCCGCCTCAGCCTCCCAAAGTGCTGGGATTATAGATGTGAACCACCATGCCCGGCCTCCCCGA CGCCCGCCTCAGCCTCCCAAAGTGCTGGGATTGTAGATGTGAACCACCATGCCCGGCCTCCCCGA T C AC006001.3 Ensembl:ENSG00000229180 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1401224727 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5251188,Human_RBP_ID_16195648,Human_RBP_ID_21557581 RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354 30493 RMVar_ID_30493 Human_SNP_ID_324248581 A-to-I Human chr7 - 66540898 66540898 66540898 GGAGTACAGTGGTACGATCTTGGCTCACTGCAACCTCTGCCTCCTGGGTTCAACTGATTCTCATG GGAGTACAGTGGTACGATCTTGGCTCACTGCAGCCTCTGCCTCCTGGGTTCAACTGATTCTCATG T C AC006001.3 Ensembl:ENSG00000229180 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1381231166 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17431013 RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354 30494 RMVar_ID_30494 Human_SNP_ID_324249297 A-to-I Human chr7 - 66542137 66542137 66542137 CTCTCTGTTGCACAGGCTATTCTTGAACTCCTAGGCTCAAGTGATCCTCCTGCTTCAGCCTCCGA CTCTCTGTTGCACAGGCTATTCTTGAACTCCTGGGCTCAAGTGATCCTCCTGCTTCAGCCTCCGA T C AC006001.3 Ensembl:ENSG00000229180 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1164583384 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16195697,Human_RBP_ID_17429232,Human_RBP_ID_22324878 Human_Splice_Rec_871377 RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354,RMVar_hsa_circ_317819,RMVar_hsa_circ_245357 30495 RMVar_ID_30495 Human_SNP_ID_324249359 A-to-I Human chr7 - 66542336 66542336 66542336 AGCCTGGCTCCTGTTTTTTGAGACAGGGTTTCACCCTGTTTCCCAGGTTGGAGTATAGTGGTGCC AGCCTGGCTCCTGTTTTTTGAGACAGGGTTTCGCCCTGTTTCCCAGGTTGGAGTATAGTGGTGCC T C AC006001.3 Ensembl:ENSG00000229180 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1281340269 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_955611,Human_RBP_ID_5222154,Human_RBP_ID_8730783,Human_RBP_ID_18109387,Human_RBP_ID_18505489,Human_RBP_ID_21557934,Human_RBP_ID_21994238,Human_RBP_ID_22425901,Human_RBP_ID_24221878 RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354,RMVar_hsa_circ_317819,RMVar_hsa_circ_245357 30496 RMVar_ID_30496 Human_SNP_ID_324249409 A-to-I Human chr7 - 66542525 66542525 66542525 TCTCGTGCATCAGCCTCCTGAGAGCTGGGACTACAGGCGCCTGCCACCACATCCGGTTAATTTTT TCTCGTGCATCAGCCTCCTGAGAGCTGGGACTGCAGGCGCCTGCCACCACATCCGGTTAATTTTT T C AC006001.3 Ensembl:ENSG00000229180 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1472537256 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16195722 Human_Splice_Rec_871373 RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354,RMVar_hsa_circ_317819,RMVar_hsa_circ_245357 30497 RMVar_ID_30497 Human_SNP_ID_324249426 A-to-I Human chr7 - 66542570 66542570 66542570 GCAGTCTCGGTTCACTGCAACCTCTGCCTCTCAGGTTCAAGCCATTCTCGTGCATCAGCCTCCTG GCAGTCTCGGTTCACTGCAACCTCTGCCTCTCGGGTTCAAGCCATTCTCGTGCATCAGCCTCCTG T C AC006001.3 Ensembl:ENSG00000229180 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1329468197 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16195729 Human_Splice_Rec_871372,Human_Splice_Rec_871373 RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354,RMVar_hsa_circ_317819,RMVar_hsa_circ_245357 30498 RMVar_ID_30498 Human_SNP_ID_324249433 A-to-I Human chr7 - 66542583 66542583 66542583 GGAGTGCAGTGGCGCAGTCTCGGTTCACTGCAACCTCTGCCTCTCAGGTTCAAGCCATTCTCGTG GGAGTGCAGTGGCGCAGTCTCGGTTCACTGCAGCCTCTGCCTCTCAGGTTCAAGCCATTCTCGTG T C AC006001.3 Ensembl:ENSG00000229180 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1294712070 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16195729,Human_RBP_ID_17429235 Human_Splice_Rec_871372,Human_Splice_Rec_871373 RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354,RMVar_hsa_circ_317819,RMVar_hsa_circ_245357 30499 RMVar_ID_30499 Human_SNP_ID_324249436 A-to-I Human chr7 - 66542589 66542589 66542589 CAGTCTGGAGTGCAGTGGCGCAGTCTCGGTTCACTGCAACCTCTGCCTCTCAGGTTCAAGCCATT CAGTCTGGAGTGCAGTGGCGCAGTCTCGGTTCGCTGCAACCTCTGCCTCTCAGGTTCAAGCCATT T C AC006001.3 Ensembl:ENSG00000229180 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1012772919 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16195729,Human_RBP_ID_17429235 Human_Splice_Rec_871372,Human_Splice_Rec_871373 RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354,RMVar_hsa_circ_317819,RMVar_hsa_circ_245357 30500 RMVar_ID_30500 Human_SNP_ID_324249696 A-to-I Human chr7 - 66543387 66543387 66543387 AGGTTGAGACAGGAGAACTGCTTGAACCCGGAAGGCAGAGGTTGCAGTGAGCCGAAATCACGCCA AGGTTGAGACAGGAGAACTGCTTGAACCCGGAGGGCAGAGGTTGCAGTGAGCCGAAATCACGCCA T C AC006001.3 Ensembl:ENSG00000229180 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348326892 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8273124,Human_RBP_ID_16195757,Human_RBP_ID_17427679 RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354,RMVar_hsa_circ_317819,RMVar_hsa_circ_245357 30501 RMVar_ID_30501 Human_SNP_ID_324249704 A-to-I Human chr7 - 66543409 66543409 66543409 CCTGTAATCCCAACTACTCAAGAGGTTGAGACAGGAGAACTGCTTGAACCCGGAAGGCAGAGGTT CCTGTAATCCCAACTACTCAAGAGGTTGAGACGGGAGAACTGCTTGAACCCGGAAGGCAGAGGTT T C AC006001.3 Ensembl:ENSG00000229180 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs943595641 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8273124,Human_RBP_ID_16195757,Human_RBP_ID_18540825,Human_RBP_ID_26111216 RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354,RMVar_hsa_circ_317819,RMVar_hsa_circ_245357 30502 RMVar_ID_30502 Human_SNP_ID_324249709 A-to-I Human chr7 - 66543436 66543436 66543436 GCAATTAGCCGAGTGTGGTGGCGGGCACCTGTAATCCCAACTACTCAAGAGGTTGAGACAGGAGA GCAATTAGCCGAGTGTGGTGGCGGGCACCTGTGATCCCAACTACTCAAGAGGTTGAGACAGGAGA T C AC006001.3 Ensembl:ENSG00000229180 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924906762 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18520105,Human_RBP_ID_18540825 RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354,RMVar_hsa_circ_317819,RMVar_hsa_circ_245357 30503 RMVar_ID_30503 Human_SNP_ID_324249725 A-to-I Human chr7 - 66543493 66543493 66543493 GAGACGGGCAGATCACCCTGGCCAACATGGCAAAACCCCATCTCTACTAAAAATACAGCAATTAG GAGACGGGCAGATCACCCTGGCCAACATGGCAGAACCCCATCTCTACTAAAAATACAGCAATTAG T C AC006001.3 Ensembl:ENSG00000229180 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs892198953 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354,RMVar_hsa_circ_317819,RMVar_hsa_circ_245357 30504 RMVar_ID_30504 Human_SNP_ID_324249789 A-to-I Human chr7 - 66543755 66543755 66543755 CTGGGAGGTGGAGGTTGCAGTGAGCAGAGATCATGTCACTGCACTGCAGCCTGGGAGACAGAGAC CTGGGAGGTGGAGGTTGCAGTGAGCAGAGATCGTGTCACTGCACTGCAGCCTGGGAGACAGAGAC T C AC006001.3 Ensembl:ENSG00000229180 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1157759938 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17427680,Human_RBP_ID_26138608 RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354,RMVar_hsa_circ_317819,RMVar_hsa_circ_245357 30505 RMVar_ID_30505 Human_SNP_ID_324249985 A-to-I Human chr7 - 66544634 66544610 66544634 GTTGCTCAGGCTGGTCTCAAACTCTTGGGCTCAGGTGATCCACCCGCCTTGGCCTCCCAAAGTGT GTTGCTCAGGCTGGTCTCAAACTCTTGGGCTC________________________CCAAAGTGT GGAGGCCAAGGCGGGTGGATCACCT G AC006001.3 Ensembl:ENSG00000229180 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1314353637 Functional Loss DEL dbSNP153 33..56 33 - - - RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354,RMVar_hsa_circ_317819,RMVar_hsa_circ_245357 30506 RMVar_ID_30506 Human_SNP_ID_324250002 A-to-I Human chr7 - 66544688 66544688 66544688 ACCACCATGCCTAGCTAATTTTTGTATTTTTTAGTAGAGACGGGTTTTCATCATGTTGCTCAGGC ACCACCATGCCTAGCTAATTTTTGTATTTTTTGGTAGAGACGGGTTTTCATCATGTTGCTCAGGC T C AC006001.3 Ensembl:ENSG00000229180 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs577334060 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8273127,Human_RBP_ID_16195789,Human_RBP_ID_18520372 RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354,RMVar_hsa_circ_317819,RMVar_hsa_circ_245357 30507 RMVar_ID_30507 Human_SNP_ID_324250013 A-to-I Human chr7 - 66544744 66544744 66544744 GGTTCAAGTGATTCTCCTGCGTCAGCCCCCCAAGTAGCTGGAATCACAGGCACCGCACCACCATG GGTTCAAGTGATTCTCCTGCGTCAGCCCCCCAGGTAGCTGGAATCACAGGCACCGCACCACCATG T C AC006001.3 Ensembl:ENSG00000229180 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs79658269 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354,RMVar_hsa_circ_317819,RMVar_hsa_circ_245357 30508 RMVar_ID_30508 Human_SNP_ID_324250014 A-to-I Human chr7 - 66544744 66544744 66544744 GGTTCAAGTGATTCTCCTGCGTCAGCCCCCCAAGTAGCTGGAATCACAGGCACCGCACCACCATG GGTTCAAGTGATTCTCCTGCGTCAGCCCCCCACGTAGCTGGAATCACAGGCACCGCACCACCATG T G AC006001.3 Ensembl:ENSG00000229180 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs79658269 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354,RMVar_hsa_circ_317819,RMVar_hsa_circ_245357 30509 RMVar_ID_30509 Human_SNP_ID_324250031 A-to-I Human chr7 - 66544790 66544790 66544790 GGAGTGCAGAGGCGCGATCTCAGCTTACTGCAACCTCCACCTCCCAGGTTCAAGTGATTCTCCTG GGAGTGCAGAGGCGCGATCTCAGCTTACTGCAGCCTCCACCTCCCAGGTTCAAGTGATTCTCCTG T C AC006001.3 Ensembl:ENSG00000229180 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1045880774 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17431015 RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354,RMVar_hsa_circ_317819,RMVar_hsa_circ_245357 30510 RMVar_ID_30510 Human_SNP_ID_324250401 A-to-I Human chr7 - 66546183 66546183 66546183 CAGGGTGGTGGTGCACACCTGTAATCCCAGCTACTTGGGAGGCTGAGGCATGAGAATGGGTTGAA CAGGGTGGTGGTGCACACCTGTAATCCCAGCTGCTTGGGAGGCTGAGGCATGAGAATGGGTTGAA T C AC006001.3 Ensembl:ENSG00000229180 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs537839473 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2177,RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354,RMVar_hsa_circ_107797,RMVar_hsa_circ_40521,RMVar_hsa_circ_245358 30511 RMVar_ID_30511 Human_SNP_ID_324250758 A-to-I Human chr7 - 66547321 66547321 66547321 GGAGAAACCCCGTCTCTTAAAAATACAAAATTAGCTTGGGTGGTGGCGCATGCTTGTAATCCCAG GGAGAAACCCCGTCTCTTAAAAATACAAAATTCGCTTGGGTGGTGGCGCATGCTTGTAATCCCAG T G AC006001.3 Ensembl:ENSG00000229180 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017090388 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17429242 RMVar_hsa_circ_2177,RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354,RMVar_hsa_circ_107797,RMVar_hsa_circ_40521,RMVar_hsa_circ_245358 30512 RMVar_ID_30512 Human_SNP_ID_324250793 A-to-I Human chr7 - 66547434 66547434 66547434 AACATTGAAGGCGGGCTGGGCGCAGTGGCTCAAGCTTGTAATCCCAGCACTTTGGGAGGCTGAGG AACATTGAAGGCGGGCTGGGCGCAGTGGCTCATGCTTGTAATCCCAGCACTTTGGGAGGCTGAGG T A AC006001.3 Ensembl:ENSG00000229180 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1254585213 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16195822 RMVar_hsa_circ_2177,RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354,RMVar_hsa_circ_107797,RMVar_hsa_circ_40521,RMVar_hsa_circ_245358 30513 RMVar_ID_30513 Human_SNP_ID_324250820 A-to-I Human chr7 - 66547508 66547508 66547508 TGCCACTGCACTCCAGTCTGGGTGATAGAGCAAGACCTCATCTCAAAAAAACAAAGAAACAATAC TGCCACTGCACTCCAGTCTGGGTGATAGAGCAGGACCTCATCTCAAAAAAACAAAGAAACAATAC T C AC006001.3 Ensembl:ENSG00000229180 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879008718 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17429243,Human_RBP_ID_18520109 RMVar_hsa_circ_2177,RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354,RMVar_hsa_circ_107797,RMVar_hsa_circ_40521,RMVar_hsa_circ_245358 30514 RMVar_ID_30514 Human_SNP_ID_324251265 A-to-I Human chr7 - 66549080 66549080 66549080 AATTGTTGTATTTTTAGTAGAGATAGGGTTTCACCATGTTGCTCAGGCTGGTCTTGAACTCCTGA AATTGTTGTATTTTTAGTAGAGATAGGGTTTCGCCATGTTGCTCAGGCTGGTCTTGAACTCCTGA T C AC006001.3 Ensembl:ENSG00000229180 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs929278199 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17431021 RMVar_hsa_circ_2177,RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354,RMVar_hsa_circ_107797,RMVar_hsa_circ_40521,RMVar_hsa_circ_245358 30515 RMVar_ID_30515 Human_SNP_ID_324251734 A-to-I Human chr7 - 66550742 66550742 66550742 CTCCGGCCTCAGCCTCCTGTGTAGCTGGGACTACAAGTGCCTACTACCACGCCTGGCTAATTTTT CTCCGGCCTCAGCCTCCTGTGTAGCTGGGACTGCAAGTGCCTACTACCACGCCTGGCTAATTTTT T C AC006001.3 Ensembl:ENSG00000229180 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1241281087 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2177,RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354,RMVar_hsa_circ_107797,RMVar_hsa_circ_40521,RMVar_hsa_circ_245358 30516 RMVar_ID_30516 Human_SNP_ID_324251754 A-to-I Human chr7 - 66550807 66550807 66550807 CAGGCAGGAGTACAGTGGCATAATCATAGCTCACTGCAGCCGTAAACTCTGGGGCTCAGGTGATC CAGGCAGGAGTACAGTGGCATAATCATAGCTCGCTGCAGCCGTAAACTCTGGGGCTCAGGTGATC T C AC006001.3 Ensembl:ENSG00000229180 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1265917094 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2177,RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354,RMVar_hsa_circ_107797,RMVar_hsa_circ_40521,RMVar_hsa_circ_245358 30517 RMVar_ID_30517 Human_SNP_ID_324251883 A-to-I Human chr7 - 66551230 66551230 66551230 ATCGCTTGAACTCAGGAGGTGGAGGTTGCAGTAAGTCAAGATTGCAAGATTGACTCCAGCCTGAG ATCGCTTGAACTCAGGAGGTGGAGGTTGCAGTTAGTCAAGATTGCAAGATTGACTCCAGCCTGAG T A AC006001.3 Ensembl:ENSG00000229180 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1221384035 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17429246 RMVar_hsa_circ_2177,RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354,RMVar_hsa_circ_107797,RMVar_hsa_circ_40521,RMVar_hsa_circ_245358 30518 RMVar_ID_30518 Human_SNP_ID_324258617 A-to-I Human chr7 - 66574184 66574184 66574184 GCCTTATTACTCAGACGTGGTGGTGTGCACCTATAGTCTCAATAACTTGGAAGGCTGAGGGATGA GCCTTATTACTCAGACGTGGTGGTGTGCACCTGTAGTCTCAATAACTTGGAAGGCTGAGGGATGA T C AC006001.3 Ensembl:ENSG00000229180 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432410792 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354,RMVar_hsa_circ_40521,RMVar_hsa_circ_26120,RMVar_hsa_circ_112926,RMVar_hsa_circ_107816,RMVar_hsa_circ_245361,RMVar_hsa_circ_277245,RMVar_hsa_circ_290650,RMVar_hsa_circ_266936,RMVar_hsa_circ_245364,RMVar_hsa_circ_245366,RMVar_hsa_circ_245365 30519 RMVar_ID_30519 Human_SNP_ID_324262019 A-to-I Human chr7 - 66586631 66586631 66586631 GGAGGATCACTTGAGTCCGGGCAGTCATGGTTATGGTGAGCTGTGATAATGCCACTGCACTCTAG GGAGGATCACTTGAGTCCGGGCAGTCATGGTTTTGGTGAGCTGTGATAATGCCACTGCACTCTAG T A AC006001.3 Ensembl:ENSG00000229180 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1394305822 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16196413 RMVar_hsa_circ_40521,RMVar_hsa_circ_26120,RMVar_hsa_circ_13427 30520 RMVar_ID_30520 Human_SNP_ID_324263049 A-to-I Human chr7 - 66590171 66590171 66590171 AGCCAGGTGTGATGGCGCCTACCTGTAATCCTAGCTACTCAGGAGGCTGAGGCAGGAGAATTGCT AGCCAGGTGTGATGGCGCCTACCTGTAATCCTGGCTACTCAGGAGGCTGAGGCAGGAGAATTGCT T C AC006001.3 Ensembl:ENSG00000229180 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1020695486 Functional Loss SNV dbSNP153 33..33 33 - - - 30521 RMVar_ID_30521 Human_SNP_ID_324263920 A-to-I Human chr7 + 66592484 66592484 66592484 TCCAAAGGTGGCGCGTGCCTGTAACCCCACCTACTAGAAAGGCTGAGGCAGGAGGATCTGTTGAA TCCAAAGGTGGCGCGTGCCTGTAACCCCACCTTCTAGAAAGGCTGAGGCAGGAGGATCTGTTGAA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1463332616 Functional Loss SNV dbSNP153 33..33 33 - - - 30522 RMVar_ID_30522 Human_SNP_ID_324267942 A-to-I Human chr7 - 66606943 66606943 66606943 TAAGATCCTAGTCGTCCGAAAATCCATTGCCCATGTTCTCACAGTTATTAACCAGACTCAGAAAG TAAGATCCTAGTCGTCCGAAAATCCATTGCCCGTGTTCTCACAGTTATTAACCAGACTCAGAAAG T C RPL35P5 Ensembl:ENSG00000225573 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879063956 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1878072 30523 RMVar_ID_30523 Human_SNP_ID_324267947 A-to-I Human chr7 - 66606957 66606957 66606957 GCCTCCAAGCTCCCTAAGATCCTAGTCGTCCGAAAATCCATTGCCCATGTTCTCACAGTTATTAA GCCTCCAAGCTCCCTAAGATCCTAGTCGTCCGGAAATCCATTGCCCATGTTCTCACAGTTATTAA T C RPL35P5 Ensembl:ENSG00000225573 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878986417 Functional Loss SNV dbSNP153 33..33 33 - - - 30524 RMVar_ID_30524 Human_SNP_ID_324276397 A-to-I Human chr7 + 66634386 66634386 66634386 GTTTTTTTTTCGGGGGCTGTTTTTTTGGAGATAGGGTCTTGCTATGTTGCCCAGGGTGGAATGTA GTTTTTTTTTCGGGGGCTGTTTTTTTGGAGATGGGGTCTTGCTATGTTGCCCAGGGTGGAATGTA A G AC027644.4,KCTD7 Ensembl:ENSG00000284461,Ensembl:ENSG00000243335 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1290078615 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_604,RMVar_hsa_circ_112691,RMVar_hsa_circ_305868,RMVar_hsa_circ_245367 30525 RMVar_ID_30525 Human_SNP_ID_324279443 A-to-I Human chr7 + 66646350 66646350 66646350 TCCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGTGCTCGCTACCACACCCGGATAATTTTT TCCCTGCCTCAGCCTCCCAAGTAGCTGGGATTGCAGGTGCTCGCTACCACACCCGGATAATTTTT A G AC027644.4,KCTD7 Ensembl:ENSG00000284461,Ensembl:ENSG00000243335 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992248476 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_245369,RMVar_hsa_circ_80384 30526 RMVar_ID_30526 Human_SNP_ID_324280606 A-to-I Human chr7 + 66650558 66650558 66650558 TAAATAGGTCAGGCGCGGTGGCTCCGGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGCGG TAAATAGGTCAGGCGCGGTGGCTCCGGCCTGTGATCCCAGCACTTTGGGAGGCTGAGGTGGGCGG A G AC027644.4 Ensembl:ENSG00000284461 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs375992325 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_245369,RMVar_hsa_circ_80384 30527 RMVar_ID_30527 Human_SNP_ID_324282452 A-to-I Human chr7 + 66656769 66656769 66656769 TTGAACCCGAGAGACAGAGGTTGTGGGGAGTCAAGATCACGCCATTGCACTCCAGCCTGGGCAAC TTGAACCCGAGAGACAGAGGTTGTGGGGAGTCGAGATCACGCCATTGCACTCCAGCCTGGGCAAC A G AC027644.4,AC006001.2 Ensembl:ENSG00000284461,Ensembl:ENSG00000226824 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs62466085 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_104,Clinvar_Rec_105 GWAS_ID_3253,GWAS_ID_3254,GWAS_ID_3255,GWAS_ID_3256,GWAS_ID_3257,GWAS_ID_3258,GWAS_ID_3259,GWAS_ID_3260,GWAS_ID_3261,GWAS_ID_3262,GWAS_ID_3263,GWAS_ID_3264,GWAS_ID_3265,GWAS_ID_3266,GWAS_ID_3267,GWAS_ID_3268,GWAS_ID_3269,GWAS_ID_3270,GWAS_ID_3271,GWAS_ID_3272,GWAS_ID_3273,GWAS_ID_3274,GWAS_ID_3275,GWAS_ID_3276,GWAS_ID_3277,GWAS_ID_3278,GWAS_ID_3279,GWAS_ID_3280,GWAS_ID_3281,GWAS_ID_3282,GWAS_ID_3283,GWAS_ID_3284,GWAS_ID_3285,GWAS_ID_3286,GWAS_ID_3287,GWAS_ID_3288,GWAS_ID_3289,GWAS_ID_3290,GWAS_ID_3291,GWAS_ID_3292,GWAS_ID_3293,GWAS_ID_3294,GWAS_ID_3295,GWAS_ID_3296,GWAS_ID_3297,GWAS_ID_3298,GWAS_ID_3299,GWAS_ID_3300,GWAS_ID_3301,GWAS_ID_3302,GWAS_ID_3303,GWAS_ID_3304,GWAS_ID_3305,GWAS_ID_3306,GWAS_ID_3307,GWAS_ID_3308,GWAS_ID_3309,GWAS_ID_3310,GWAS_ID_3311,GWAS_ID_3312,GWAS_ID_3313,GWAS_ID_3314,GWAS_ID_3315,GWAS_ID_3316,GWAS_ID_3317,GWAS_ID_3318,GWAS_ID_3319,GWAS_ID_3320,GWAS_ID_3321,GWAS_ID_3322,GWAS_ID_3323,GWAS_ID_3324,GWAS_ID_3325,GWAS_ID_3326,GWAS_ID_3327,GWAS_ID_3328,GWAS_ID_3329,GWAS_ID_3330,GWAS_ID_3331,GWAS_ID_3332,GWAS_ID_3333,GWAS_ID_3334,GWAS_ID_3335,GWAS_ID_3336,GWAS_ID_3337,GWAS_ID_3338,GWAS_ID_3339,GWAS_ID_3340,GWAS_ID_3341,GWAS_ID_3342,GWAS_ID_3343,GWAS_ID_3344,GWAS_ID_3345,GWAS_ID_3346,GWAS_ID_3347,GWAS_ID_3348,GWAS_ID_3349,GWAS_ID_3350,GWAS_ID_3351,GWAS_ID_3352,GWAS_ID_3353,GWAS_ID_3354,GWAS_ID_3355,GWAS_ID_3356,GWAS_ID_3357,GWAS_ID_3358,GWAS_ID_3359,GWAS_ID_3360,GWAS_ID_3361,GWAS_ID_3362,GWAS_ID_3363,GWAS_ID_3364,GWAS_ID_3365,GWAS_ID_3366,GWAS_ID_3367,GWAS_ID_3368,GWAS_ID_3369,GWAS_ID_3370,GWAS_ID_3371,GWAS_ID_3372,GWAS_ID_3373,GWAS_ID_3374,GWAS_ID_3375,GWAS_ID_3376,GWAS_ID_3377,GWAS_ID_3378,GWAS_ID_3379,GWAS_ID_3380,GWAS_ID_3381,GWAS_ID_3382,GWAS_ID_3383,GWAS_ID_3384,GWAS_ID_3385,GWAS_ID_3386,GWAS_ID_3387,GWAS_ID_3388,GWAS_ID_3389,GWAS_ID_3390,GWAS_ID_3391,GWAS_ID_3392,GWAS_ID_3393,GWAS_ID_3394,GWAS_ID_3395,GWAS_ID_3396,GWAS_ID_3397,GWAS_ID_3398,GWAS_ID_3399,GWAS_ID_3400,GWAS_ID_3401,GWAS_ID_3402,GWAS_ID_3403,GWAS_ID_3404,GWAS_ID_3405,GWAS_ID_3406,GWAS_ID_3407,GWAS_ID_3408,GWAS_ID_3409,GWAS_ID_3410,GWAS_ID_3411,GWAS_ID_3412,GWAS_ID_3413 RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_245369,RMVar_hsa_circ_80384 30528 RMVar_ID_30528 Human_SNP_ID_324286663 A-to-I Human chr7 + 66672013 66672013 66672013 TAATTTTTGATTTTTTGTAGGAATGAGGTTTCAGTATGTTGGCCAGGATGTTCTTGAACTCCTGG TAATTTTTGATTTTTTGTAGGAATGAGGTTTCGGTATGTTGGCCAGGATGTTCTTGAACTCCTGG A G AC027644.4 Ensembl:ENSG00000284461 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251911979 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_245369,RMVar_hsa_circ_80384 30529 RMVar_ID_30529 Human_SNP_ID_324289004 A-to-I Human chr7 - 66681530 66681530 66681530 GCCGGGCATGATGGCGGGCACCTGTGGTCCCAACTACTGGGGAGGCTGAGGTGGGAGGATCGCTT GCCGGGCATGATGGCGGGCACCTGTGGTCCCATCTACTGGGGAGGCTGAGGTGGGAGGATCGCTT T A RF00017-4513 RNACentral:URS000090EECB SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946465180 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23315515 30530 RMVar_ID_30530 Human_SNP_ID_324290024 A-to-I Human chr7 + 66684761 66684761 66684761 GGTTCATGCCATTCTCCTGCTTCAGTCTCCCGAGTAGCTGGGACTGCAGGCACCCGCCACCATGC GGTTCATGCCATTCTCCTGCTTCAGTCTCCCGGGTAGCTGGGACTGCAGGCACCCGCCACCATGC A G AC027644.4,RABGEF1 Ensembl:ENSG00000284461,Ensembl:ENSG00000154710 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1186403003 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_245369,RMVar_hsa_circ_80384 30531 RMVar_ID_30531 Human_SNP_ID_324290066 A-to-I Human chr7 + 66684896 66684896 66684896 TGACCTCGTGGTCTGCCCGCTTCGGCCTTCCAAAGTGTTGGGATTACAGGCGTGAGCCACTGTAT TGACCTCGTGGTCTGCCCGCTTCGGCCTTCCAGAGTGTTGGGATTACAGGCGTGAGCCACTGTAT A G AC027644.4,RABGEF1 Ensembl:ENSG00000284461,Ensembl:ENSG00000154710 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1306336908 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8670110 RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_245369,RMVar_hsa_circ_80384 30532 RMVar_ID_30532 Human_SNP_ID_324290092 A-to-I Human chr7 + 66684999 66684999 66684999 GTTTCCCAGGGTGGTCTCCAACCCCTGGCCTCAAGTGATTCTCTAGCCTTGGACTCCCAAAGTGT GTTTCCCAGGGTGGTCTCCAACCCCTGGCCTCGAGTGATTCTCTAGCCTTGGACTCCCAAAGTGT A G AC027644.4,RABGEF1 Ensembl:ENSG00000284461,Ensembl:ENSG00000154710 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs192262086 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16196841 RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_245369,RMVar_hsa_circ_80384 30533 RMVar_ID_30533 Human_SNP_ID_324290177 A-to-I Human chr7 + 66685271 66685271 66685271 CACCTCCTGGGTTCAAGTGATTCGCCTGCCTCAGCCTTCTGAGTACCTGGGAATATAGGCACTCG CACCTCCTGGGTTCAAGTGATTCGCCTGCCTCGGCCTTCTGAGTACCTGGGAATATAGGCACTCG A G AC027644.4,RABGEF1 Ensembl:ENSG00000284461,Ensembl:ENSG00000154710 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs3194900 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_245369,RMVar_hsa_circ_80384 30534 RMVar_ID_30534 Human_SNP_ID_324290709 A-to-I Human chr7 + 66687254 66687254 66687254 TTCAAGCAGTCCTCCTGCCTCGGCCCCCCAGTAGGTGGGATTACAGGCATGCACCACCATGCCTT TTCAAGCAGTCCTCCTGCCTCGGCCCCCCAGTGGGTGGGATTACAGGCATGCACCACCATGCCTT A G AC027644.4,RABGEF1 Ensembl:ENSG00000284461,Ensembl:ENSG00000154710 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1453539319 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_245369,RMVar_hsa_circ_80384 30535 RMVar_ID_30535 Human_SNP_ID_324292932 A-to-I Human chr7 + 66695923 66695923 66695923 GGGAGTCGGAGGTTGCAGTGAGCTGAGATCGCACCACCGTACTTCAGCGTGGGTAACAAAGCGAG GGGAGTCGGAGGTTGCAGTGAGCTGAGATCGCGCCACCGTACTTCAGCGTGGGTAACAAAGCGAG A G AC027644.4,RABGEF1 Ensembl:ENSG00000284461,Ensembl:ENSG00000154710 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1387076354 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_245369,RMVar_hsa_circ_80384 30536 RMVar_ID_30536 Human_SNP_ID_324294677 A-to-I Human chr7 + 66702992 66702989 66702992 TATCTAAGTTTTTTTGTTTGTTTGTTTTTGAGAAGGAGTCTCGCTCTGTCGCCGCCCAGGCTGGA TATCTAAGTTTTTTTGTTTGTTTGTTTTTG___AGGAGTCTCGCTCTGTCGCCGCCCAGGCTGGA GAGA G AC027644.4,RABGEF1 Ensembl:ENSG00000284461,Ensembl:ENSG00000154710 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1366883302 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_16197120 RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_245369,RMVar_hsa_circ_80384 30537 RMVar_ID_30537 Human_SNP_ID_324294698 A-to-I Human chr7 + 66703038 66703038 66703038 TGTCGCCGCCCAGGCTGGAGGGCAGTGGTGCTATCTCAACTTACTGCAAGCTCTGCCTCCTGGGT TGTCGCCGCCCAGGCTGGAGGGCAGTGGTGCTGTCTCAACTTACTGCAAGCTCTGCCTCCTGGGT A G AC027644.4,RABGEF1 Ensembl:ENSG00000284461,Ensembl:ENSG00000154710 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1311325474 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_245369,RMVar_hsa_circ_80384 30538 RMVar_ID_30538 Human_SNP_ID_324294714 A-to-I Human chr7 + 66703099 66703099 66703099 GGGTTCACTCCATTCTCCTGCCTCAGCCTCCCAAGTAGTTGGGACTATAGGCGCCCGCTACCATG GGGTTCACTCCATTCTCCTGCCTCAGCCTCCCGAGTAGTTGGGACTATAGGCGCCCGCTACCATG A G AC027644.4,RABGEF1 Ensembl:ENSG00000284461,Ensembl:ENSG00000154710 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1272160299 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_245369,RMVar_hsa_circ_80384 30539 RMVar_ID_30539 Human_SNP_ID_324294717 A-to-I Human chr7 + 66703103 66703103 66703103 TCACTCCATTCTCCTGCCTCAGCCTCCCAAGTAGTTGGGACTATAGGCGCCCGCTACCATGCCTG TCACTCCATTCTCCTGCCTCAGCCTCCCAAGTCGTTGGGACTATAGGCGCCCGCTACCATGCCTG A C AC027644.4,RABGEF1 Ensembl:ENSG00000284461,Ensembl:ENSG00000154710 Protein coding,Protein coding intron,intron GSE100210;GSE107867 HepG2 cell line;ASD brains,temporal_cortex - 29129909,30559470 RNA-Seq:(High) rs979805725 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_245369,RMVar_hsa_circ_80384 30540 RMVar_ID_30540 Human_SNP_ID_324294760 A-to-I Human chr7 + 66703252 66703252 66703252 CCTTGGCCTCCCAAAGTGCTGGGATTACAGGTATGAGCCACCGTGCCTGGCCTGTATGTAAGTTT CCTTGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGTGCCTGGCCTGTATGTAAGTTT A G AC027644.4,RABGEF1 Ensembl:ENSG00000284461,Ensembl:ENSG00000154710 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs776464283 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_245369,RMVar_hsa_circ_80384 30541 RMVar_ID_30541 Human_SNP_ID_324295213 A-to-I Human chr7 + 66705222 66705221 66705222 CAGGAGTTCGAAACAAGCTTGGCCAACATGGTAAAACCCCGTCTGTACTAAAAATGCAAAAAATT CAGGAGTTCGAAACAAGCTTGGCCAACATGGT_AAACCCCGTCTGTACTAAAAATGCAAAAAATT TA T AC027644.4,RABGEF1 Ensembl:ENSG00000284461,Ensembl:ENSG00000154710 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264415715 Functional Loss DEL dbSNP153 33..33 33 - - - Human_miRNA_ID_2277944,Human_miRNA_ID_2709732 RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_245369,RMVar_hsa_circ_80384 30542 RMVar_ID_30542 Human_SNP_ID_324295724 A-to-I Human chr7 + 66706682 66706682 66706682 ATGATCCGCCCGCCTCGGCCTCCCAAAGTGCTAGGATTACAGGTGTGAGCCACCGCGCCTAGCTG ATGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCGCCTAGCTG A G AC027644.4,RABGEF1 Ensembl:ENSG00000284461,Ensembl:ENSG00000154710 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs375077101 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2450040 RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_245369,RMVar_hsa_circ_80384 30543 RMVar_ID_30543 Human_SNP_ID_324295727 A-to-I Human chr7 + 66706688 66706688 66706688 CGCCCGCCTCGGCCTCCCAAAGTGCTAGGATTACAGGTGTGAGCCACCGCGCCTAGCTGACTCAA CGCCCGCCTCGGCCTCCCAAAGTGCTAGGATTGCAGGTGTGAGCCACCGCGCCTAGCTGACTCAA A G AC027644.4,RABGEF1 Ensembl:ENSG00000284461,Ensembl:ENSG00000154710 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1457298810 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2450040 RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_245369,RMVar_hsa_circ_80384 30544 RMVar_ID_30544 Human_SNP_ID_324296004 A-to-I Human chr7 + 66707629 66707629 66707629 AAAATTGCTTGAACCTGGGAGGTGGAAGTTGCAGTGAGCCGAGACTGCACCACTGCACTCCAGAC AAAATTGCTTGAACCTGGGAGGTGGAAGTTGCGGTGAGCCGAGACTGCACCACTGCACTCCAGAC A G AC027644.4,RABGEF1 Ensembl:ENSG00000284461,Ensembl:ENSG00000154710 Protein coding,Protein coding intron,intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1257970765 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_245369,RMVar_hsa_circ_80384 30545 RMVar_ID_30545 Human_SNP_ID_324296010 A-to-I Human chr7 + 66707645 66707645 66707645 GGGAGGTGGAAGTTGCAGTGAGCCGAGACTGCACCACTGCACTCCAGACTGGGCAAAAGAGCAAG GGGAGGTGGAAGTTGCAGTGAGCCGAGACTGCGCCACTGCACTCCAGACTGGGCAAAAGAGCAAG A G AC027644.4,RABGEF1 Ensembl:ENSG00000284461,Ensembl:ENSG00000154710 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1267845519 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2792344 RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_245369,RMVar_hsa_circ_80384 30546 RMVar_ID_30546 Human_SNP_ID_324296016 A-to-I Human chr7 + 66707675 66707674 66707676 GCACCACTGCACTCCAGACTGGGCAAAAGAGCAAGACTCCATCTCAACAACAACAAAAAGAGTAT GCACCACTGCACTCCAGACTGGGCAAAAGAGC__GACTCCATCTCAACAACAACAAAAAGAGTAT CAA C AC027644.4,RABGEF1 Ensembl:ENSG00000284461,Ensembl:ENSG00000154710 Protein coding,Protein coding intron,intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs568969872 Functional Loss DEL dbSNP153 33..34 33 - - - Human_miRNA_ID_2611058 RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_245369,RMVar_hsa_circ_80384 30547 RMVar_ID_30547 Human_SNP_ID_324297674 A-to-I Human chr7 + 66715164 66715164 66715164 TTTCTTCTTCTCCTGAGACAGGGTCTCACTCTATCACCTAGGCTGGAGTACCATGACAGGATCCT TTTCTTCTTCTCCTGAGACAGGGTCTCACTCTGTCACCTAGGCTGGAGTACCATGACAGGATCCT A G AC027644.4,RABGEF1 Ensembl:ENSG00000284461,Ensembl:ENSG00000154710 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941444437 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21554252 RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_18303,RMVar_hsa_circ_245369,RMVar_hsa_circ_80384,RMVar_hsa_circ_304006 30548 RMVar_ID_30548 Human_SNP_ID_324297825 A-to-I Human chr7 + 66715831 66715831 66715831 AGTGGCTATTCCCAGCACAATCATAGTGCACTACAGTCTCCAACTCCTGGGTTCAGGTGCTCCTT AGTGGCTATTCCCAGCACAATCATAGTGCACTGCAGTCTCCAACTCCTGGGTTCAGGTGCTCCTT A G AC027644.4,RABGEF1 Ensembl:ENSG00000284461,Ensembl:ENSG00000154710 Protein coding,Protein coding intron,intron GSE123020:GSM3490829,GSM3490830,GSM3490831 esophageal squamous carcinoma cells,EC109 cell line - 32596459 RNA-Seq:(High) rs925587237 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_18303,RMVar_hsa_circ_245369,RMVar_hsa_circ_80384,RMVar_hsa_circ_304006 30549 RMVar_ID_30549 Human_SNP_ID_324297958 A-to-I Human chr7 + 66716480 66716480 66716480 AAAATTAGCTAGGTGTGGCGGCATGTGCCTGTAGTCCTAGCTACTCAGGAGGCTGAGGCATGAGG AAAATTAGCTAGGTGTGGCGGCATGTGCCTGTGGTCCTAGCTACTCAGGAGGCTGAGGCATGAGG A G AC027644.4,RABGEF1 Ensembl:ENSG00000284461,Ensembl:ENSG00000154710 Protein coding,Protein coding intron,intron GSE100210;GSE99789 HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 29129909,29796672 RNA-Seq:(High) rs1178155831 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_18303,RMVar_hsa_circ_245369,RMVar_hsa_circ_80384,RMVar_hsa_circ_304006 30550 RMVar_ID_30550 Human_SNP_ID_324303789 A-to-I Human chr7 - 66740094 66740094 66740094 CATGATGGCGGGCACCTGTGGTCCCAACTACCAGGGAGGCTGAGGTGGGAGGATCGCTTGATAGC CATGATGGCGGGCACCTGTGGTCCCAACTACCGGGGAGGCTGAGGTGGGAGGATCGCTTGATAGC T C AC027644.3 Ensembl:ENSG00000272831 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs528135374 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18103047 30551 RMVar_ID_30551 Human_SNP_ID_324303790 A-to-I Human chr7 - 66740097 66740097 66740097 GGACATGATGGCGGGCACCTGTGGTCCCAACTACCAGGGAGGCTGAGGTGGGAGGATCGCTTGAT GGACATGATGGCGGGCACCTGTGGTCCCAACTGCCAGGGAGGCTGAGGTGGGAGGATCGCTTGAT T C AC027644.3 Ensembl:ENSG00000272831 lincRNA exon GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1133794 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4946896,Human_RBP_ID_18103047 30552 RMVar_ID_30552 Human_SNP_ID_324303792 A-to-I Human chr7 - 66740100 66740100 66740100 GCCGGACATGATGGCGGGCACCTGTGGTCCCAACTACCAGGGAGGCTGAGGTGGGAGGATCGCTT GCCGGACATGATGGCGGGCACCTGTGGTCCCAGCTACCAGGGAGGCTGAGGTGGGAGGATCGCTT T C AC027644.3 Ensembl:ENSG00000272831 lincRNA exon GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1194164095 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18103047 30553 RMVar_ID_30553 Human_SNP_ID_324304382 A-to-I Human chr7 + 66741731 66741731 66741731 TATTTATTATTTTTTTCGACATGGGATCTCACAGTGTTGCCCAGGCAGGTGTGAAACTCCTGGCC TATTTATTATTTTTTTCGACATGGGATCTCACGGTGTTGCCCAGGCAGGTGTGAAACTCCTGGCC A G AC027644.4,RABGEF1 Ensembl:ENSG00000284461,Ensembl:ENSG00000154710 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs891141693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2059608,Human_miRNA_ID_2185005,Human_miRNA_ID_2672353 RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_18303,RMVar_hsa_circ_245369,RMVar_hsa_circ_80384 30554 RMVar_ID_30554 Human_SNP_ID_324304653 A-to-I Human chr7 + 66742630 66742630 66742630 GGAGGTGCCTATTAATTTATTTATTGAGAGAGAGGGTCTCACTTTGTCACCCAGGCTGGAGTACA GGAGGTGCCTATTAATTTATTTATTGAGAGAGCGGGTCTCACTTTGTCACCCAGGCTGGAGTACA A C AC027644.4,RABGEF1 Ensembl:ENSG00000284461,Ensembl:ENSG00000154710 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1235955878 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2845418,Human_miRNA_ID_2848438 RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_18303,RMVar_hsa_circ_245369,RMVar_hsa_circ_80384 30555 RMVar_ID_30555 Human_SNP_ID_324304735 A-to-I Human chr7 + 66742887 66742887 66742887 CCTCAAGCGTCCCAAGTGCTGAAATTACAGGCATCAGCTACCGAGCCTGGAGGGTCGTTACTAAA CCTCAAGCGTCCCAAGTGCTGAAATTACAGGCTTCAGCTACCGAGCCTGGAGGGTCGTTACTAAA A T AC027644.4,RABGEF1 Ensembl:ENSG00000284461,Ensembl:ENSG00000154710 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1297574867 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_18303,RMVar_hsa_circ_245369,RMVar_hsa_circ_80384 30556 RMVar_ID_30556 Human_SNP_ID_324304843 A-to-I Human chr7 + 66743196 66743196 66743196 TTGGTGTGATGGCGCCTGCCGTAATGCTAGCTACTCAGGAGGCTGAGGTAGGAGAATTGCTTGAA TTGGTGTGATGGCGCCTGCCGTAATGCTAGCTGCTCAGGAGGCTGAGGTAGGAGAATTGCTTGAA A G AC027644.4,RABGEF1 Ensembl:ENSG00000284461,Ensembl:ENSG00000154710 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1175790732 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_18303,RMVar_hsa_circ_245369,RMVar_hsa_circ_80384 30557 RMVar_ID_30557 Human_SNP_ID_324304851 A-to-I Human chr7 + 66743213 66743213 66743213 GCCGTAATGCTAGCTACTCAGGAGGCTGAGGTAGGAGAATTGCTTGAACCTAGCAATTCTAGGAG GCCGTAATGCTAGCTACTCAGGAGGCTGAGGTGGGAGAATTGCTTGAACCTAGCAATTCTAGGAG A G AC027644.4,RABGEF1 Ensembl:ENSG00000284461,Ensembl:ENSG00000154710 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1160580289 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2742340 RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_18303,RMVar_hsa_circ_245369,RMVar_hsa_circ_80384 30558 RMVar_ID_30558 Human_SNP_ID_324304862 A-to-I Human chr7 + 66743267 66743267 66743267 AATTCTAGGAGGTTGTGGTGAGCCAAGATTGTACCAATGCACTCCAGCCTGGGCGACAGAGCGAG AATTCTAGGAGGTTGTGGTGAGCCAAGATTGTGCCAATGCACTCCAGCCTGGGCGACAGAGCGAG A G AC027644.4,RABGEF1 Ensembl:ENSG00000284461,Ensembl:ENSG00000154710 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs560245347 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23077522,Human_RBP_ID_26138636 RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_18303,RMVar_hsa_circ_245369,RMVar_hsa_circ_80384 30559 RMVar_ID_30559 Human_SNP_ID_324305013 A-to-I Human chr7 + 66743762 66743762 66743762 TGACCTCGTGATCCGCCCTCCTCGGCATTCCAAAGTGCTGGGATTACAGGTGTGAGCCACCACAC TGACCTCGTGATCCGCCCTCCTCGGCATTCCATAGTGCTGGGATTACAGGTGTGAGCCACCACAC A T AC027644.4,RABGEF1 Ensembl:ENSG00000284461,Ensembl:ENSG00000154710 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs558075885 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22620392 RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_18303,RMVar_hsa_circ_245369,RMVar_hsa_circ_80384 30560 RMVar_ID_30560 Human_SNP_ID_324305016 A-to-I Human chr7 + 66743775 66743775 66743775 CGCCCTCCTCGGCATTCCAAAGTGCTGGGATTACAGGTGTGAGCCACCACACTTGGGCTAAATTT CGCCCTCCTCGGCATTCCAAAGTGCTGGGATTGCAGGTGTGAGCCACCACACTTGGGCTAAATTT A G AC027644.4,RABGEF1 Ensembl:ENSG00000284461,Ensembl:ENSG00000154710 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1337225208 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22620392 RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_18303,RMVar_hsa_circ_245369,RMVar_hsa_circ_80384 30561 RMVar_ID_30561 Human_SNP_ID_324305054 A-to-I Human chr7 + 66743907 66743907 66743907 CTAGCCTCGGCCTCCCAAAGTGTTGGGATTACAAACATGAGCCACTGCACCCGGCCCTAAAATGG CTAGCCTCGGCCTCCCAAAGTGTTGGGATTACGAACATGAGCCACTGCACCCGGCCCTAAAATGG A G AC027644.4,RABGEF1 Ensembl:ENSG00000284461,Ensembl:ENSG00000154710 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1403989151 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16197670 RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_18303,RMVar_hsa_circ_245369,RMVar_hsa_circ_80384 30562 RMVar_ID_30562 Human_SNP_ID_324305104 A-to-I Human chr7 + 66744056 66744056 66744056 TTCTTTTCTTTTCTTTTCTTTTTTTTTTTTTTAAGACGGAGTCTTGATCTGTGACTGGGCTGGAG TTCTTTTCTTTTCTTTTCTTTTTTTTTTTTTTTAGACGGAGTCTTGATCTGTGACTGGGCTGGAG A T AC027644.4,RABGEF1 Ensembl:ENSG00000284461,Ensembl:ENSG00000154710 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1315037459 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16197678,Human_RBP_ID_22483510 RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_18303,RMVar_hsa_circ_245369,RMVar_hsa_circ_80384 30563 RMVar_ID_30563 Human_SNP_ID_324305122 A-to-I Human chr7 + 66744110 66744110 66744110 CTGGGCTGGAGTGCAGTGGCATGATCTTGGCCACTGCAACCTCTGCCTCCTGGATTCAAGCGATT CTGGGCTGGAGTGCAGTGGCATGATCTTGGCCGCTGCAACCTCTGCCTCCTGGATTCAAGCGATT A G AC027644.4,RABGEF1 Ensembl:ENSG00000284461,Ensembl:ENSG00000154710 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs557746368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16197680 Human_miRNA_ID_2272162,Human_miRNA_ID_2474978,Human_miRNA_ID_2960765 RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_18303,RMVar_hsa_circ_245369,RMVar_hsa_circ_80384 30564 RMVar_ID_30564 Human_SNP_ID_324305135 A-to-I Human chr7 + 66744153 66744153 66744153 TGCCTCCTGGATTCAAGCGATTTGTGTGCCTCAGCCTTCTGAGTAGCTGGGACTGACCATAGATA TGCCTCCTGGATTCAAGCGATTTGTGTGCCTCGGCCTTCTGAGTAGCTGGGACTGACCATAGATA A G AC027644.4,RABGEF1 Ensembl:ENSG00000284461,Ensembl:ENSG00000154710 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1454475277 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16197683 RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_18303,RMVar_hsa_circ_245369,RMVar_hsa_circ_80384 30565 RMVar_ID_30565 Human_SNP_ID_324305635 A-to-I Human chr7 + 66745837 66745837 66745837 AGAGTTTCAGGCTGGTGCAGTGGCTCATGCCTATAATACCAGTGCTTTGGGAGGCCAAAGTGGGA AGAGTTTCAGGCTGGTGCAGTGGCTCATGCCTGTAATACCAGTGCTTTGGGAGGCCAAAGTGGGA A G AC027644.4,RABGEF1 Ensembl:ENSG00000284461,Ensembl:ENSG00000154710 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs567168267 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_18303,RMVar_hsa_circ_245369,RMVar_hsa_circ_80384 30566 RMVar_ID_30566 Human_SNP_ID_324305882 A-to-I Human chr7 + 66746710 66746710 66746710 TGGTGGCACGATCTCTACTCACTGCAACTTCCACCTCCCCGGTTCAAGCGATTCTTGTGCCTCAG TGGTGGCACGATCTCTACTCACTGCAACTTCCGCCTCCCCGGTTCAAGCGATTCTTGTGCCTCAG A G AC027644.4,RABGEF1 Ensembl:ENSG00000284461,Ensembl:ENSG00000154710 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1395646980 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_18303,RMVar_hsa_circ_245369,RMVar_hsa_circ_80384 30567 RMVar_ID_30567 Human_SNP_ID_324308101 A-to-I Human chr7 + 66755106 66755106 66755106 CACGAGGTCAGGATATTGAGACCATCCTGGCTAACACAGTAAAACCTGGTCTCTACTAAAAATAC CACGAGGTCAGGATATTGAGACCATCCTGGCTGACACAGTAAAACCTGGTCTCTACTAAAAATAC A G AC027644.4,RABGEF1 Ensembl:ENSG00000284461,Ensembl:ENSG00000154710 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1168726403 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_18303,RMVar_hsa_circ_245369,RMVar_hsa_circ_80384 30568 RMVar_ID_30568 Human_SNP_ID_324309914 A-to-I Human chr7 + 66762333 66762333 66762333 GACATGGAGGCTGGGTGCAGTGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCCAAGGTGGGT GACATGGAGGCTGGGTGCAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGT A G AC027644.4,RABGEF1 Ensembl:ENSG00000284461,Ensembl:ENSG00000154710 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs533064057 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_18303,RMVar_hsa_circ_245369,RMVar_hsa_circ_80384 30569 RMVar_ID_30569 Human_SNP_ID_324313119 A-to-I Human chr7 + 66775310 66775310 66775310 GGCCCAATCCCTCACATTCTCCAAGTTTGAAGAAAAGAAAACCAACGAGAAGACCCGCAAGGTTA GGCCCAATCCCTCACATTCTCCAAGTTTGAAGGAAAGAAAACCAACGAGAAGACCCGCAAGGTTA A G AC027644.4,RABGEF1 Ensembl:ENSG00000284461,Ensembl:ENSG00000154710 Protein coding,Protein coding 3'UTR,CDS GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs778572706 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8271961,Human_RBP_ID_9403397,Human_RBP_ID_24549111 Human_Splice_Rec_871476,Human_Splice_Rec_871477,Human_Splice_Rec_871530,Human_Splice_Rec_871531,Human_Splice_Rec_871544,Human_Splice_Rec_871545,Human_Splice_Rec_871558,Human_Splice_Rec_871576,Human_Splice_Rec_871577,Human_Splice_Rec_871592,Human_Splice_Rec_871593,Human_Splice_Rec_871608,Human_Splice_Rec_871609,Human_Splice_Rec_871624,Human_Splice_Rec_871625,Human_Splice_Rec_871640,Human_Splice_Rec_871641 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_245373,RMVar_hsa_circ_245377,RMVar_hsa_circ_293552,RMVar_hsa_circ_245371,RMVar_hsa_circ_12986,RMVar_hsa_circ_320004,RMVar_hsa_circ_377698,RMVar_hsa_circ_300161,RMVar_hsa_circ_278920,RMVar_hsa_circ_284379,RMVar_hsa_circ_273398,RMVar_hsa_circ_245375,RMVar_hsa_circ_245376,RMVar_hsa_circ_245374,RMVar_hsa_circ_245380,RMVar_hsa_circ_306660,RMVar_hsa_circ_245378,RMVar_hsa_circ_245372,RMVar_hsa_circ_377787,RMVar_hsa_circ_319250,RMVar_hsa_circ_378697,RMVar_hsa_circ_274362,RMVar_hsa_circ_306573,RMVar_hsa_circ_245381,RMVar_hsa_circ_245379 30570 RMVar_ID_30570 Human_SNP_ID_324319306 A-to-I Human chr7 + 66802101 66802100 66802102 CCAGCTAATTTTTGTTTACATTCTGTAGAGACAGAGTTTCATCATGTTGCCTTGGCTGCTCTTGA CCAGCTAATTTTTGTTTACATTCTGTAGAGAC__AGTTTCATCATGTTGCCTTGGCTGCTCTTGA CAG C AC027644.4,RABGEF1 Ensembl:ENSG00000284461,Ensembl:ENSG00000154710 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947994033 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_11472,RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_245373,RMVar_hsa_circ_12986,RMVar_hsa_circ_377698,RMVar_hsa_circ_300161,RMVar_hsa_circ_245378,RMVar_hsa_circ_245372,RMVar_hsa_circ_377787,RMVar_hsa_circ_319250,RMVar_hsa_circ_278625,RMVar_hsa_circ_126240,RMVar_hsa_circ_245383,RMVar_hsa_circ_279002,RMVar_hsa_circ_245385,RMVar_hsa_circ_245386,RMVar_hsa_circ_271655 30571 RMVar_ID_30571 Human_SNP_ID_324319307 A-to-I Human chr7 + 66802101 66802101 66802101 CCAGCTAATTTTTGTTTACATTCTGTAGAGACAGAGTTTCATCATGTTGCCTTGGCTGCTCTTGA CCAGCTAATTTTTGTTTACATTCTGTAGAGACCGAGTTTCATCATGTTGCCTTGGCTGCTCTTGA A C AC027644.4,RABGEF1 Ensembl:ENSG00000284461,Ensembl:ENSG00000154710 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1414848022 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11472,RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_245373,RMVar_hsa_circ_12986,RMVar_hsa_circ_377698,RMVar_hsa_circ_300161,RMVar_hsa_circ_245378,RMVar_hsa_circ_245372,RMVar_hsa_circ_377787,RMVar_hsa_circ_319250,RMVar_hsa_circ_278625,RMVar_hsa_circ_126240,RMVar_hsa_circ_245383,RMVar_hsa_circ_279002,RMVar_hsa_circ_245385,RMVar_hsa_circ_245386,RMVar_hsa_circ_271655 30572 RMVar_ID_30572 Human_SNP_ID_324319755 A-to-I Human chr7 + 66804183 66804183 66804183 GTAGCTCACTGCAGCCTCAACCTCTTGGGCTCAAGCCATCCTTCTGCCTCAGCCTTTCCAGTAGT GTAGCTCACTGCAGCCTCAACCTCTTGGGCTCCAGCCATCCTTCTGCCTCAGCCTTTCCAGTAGT A C AC027644.4,RABGEF1 Ensembl:ENSG00000284461,Ensembl:ENSG00000154710 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs950180295 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2042822,Human_miRNA_ID_2044973 RMVar_hsa_circ_11472,RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_245373,RMVar_hsa_circ_12986,RMVar_hsa_circ_377698,RMVar_hsa_circ_300161,RMVar_hsa_circ_245378,RMVar_hsa_circ_245372,RMVar_hsa_circ_377787,RMVar_hsa_circ_319250,RMVar_hsa_circ_278625,RMVar_hsa_circ_126240,RMVar_hsa_circ_245383,RMVar_hsa_circ_279002,RMVar_hsa_circ_245385,RMVar_hsa_circ_245386,RMVar_hsa_circ_271655 30573 RMVar_ID_30573 Human_SNP_ID_324330388 A-to-I Human chr7 + 66846588 66846588 66846588 ATGGCAAAACCATTATCTCTACTAAAAAAATTAGCTAGGTATGCTACGCTCCTATAATCCCTGCT ATGGCAAAACCATTATCTCTACTAAAAAAATTTGCTAGGTATGCTACGCTCCTATAATCCCTGCT A T lnc-TMEM248-4 RNACentral:URS00008B849C lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1222920623 Functional Loss SNV dbSNP153 33..33 33 - - - 30574 RMVar_ID_30574 Human_SNP_ID_324330393 A-to-I Human chr7 + 66846609 66846609 66846609 CTAAAAAAATTAGCTAGGTATGCTACGCTCCTATAATCCCTGCTATTCGGGAGGCTGAGGCAGGA CTAAAAAAATTAGCTAGGTATGCTACGCTCCTGTAATCCCTGCTATTCGGGAGGCTGAGGCAGGA A G lnc-TMEM248-4 RNACentral:URS00008B849C lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs532835382 Functional Loss SNV dbSNP153 33..33 33 - - - 30575 RMVar_ID_30575 Human_SNP_ID_324330395 A-to-I Human chr7 + 66846621 66846621 66846621 GCTAGGTATGCTACGCTCCTATAATCCCTGCTATTCGGGAGGCTGAGGCAGGAGAATCGTTTGAA GCTAGGTATGCTACGCTCCTATAATCCCTGCTTTTCGGGAGGCTGAGGCAGGAGAATCGTTTGAA A T lnc-TMEM248-4 RNACentral:URS00008B849C lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355369448 Functional Loss SNV dbSNP153 33..33 33 - - - 30576 RMVar_ID_30576 Human_SNP_ID_324330508 A-to-I Human chr7 + 66846994 66846994 66846994 ACTCTGTCACCCAGGCTGGAGGGCAGTGGCACAATCTCAGCTCACTGCAACCTTCACCCCCTCCC ACTCTGTCACCCAGGCTGGAGGGCAGTGGCACGATCTCAGCTCACTGCAACCTTCACCCCCTCCC A G lnc-TMEM248-4 RNACentral:URS00008B849C lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1393904656 Functional Loss SNV dbSNP153 33..33 33 - - - 30577 RMVar_ID_30577 Human_SNP_ID_324330509 A-to-I Human chr7 + 66847000 66847000 66847000 TCACCCAGGCTGGAGGGCAGTGGCACAATCTCAGCTCACTGCAACCTTCACCCCCTCCCCGCCCC TCACCCAGGCTGGAGGGCAGTGGCACAATCTCCGCTCACTGCAACCTTCACCCCCTCCCCGCCCC A C lnc-TMEM248-4 RNACentral:URS00008B849C lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1343583701 Functional Loss SNV dbSNP153 33..33 33 - - - 30578 RMVar_ID_30578 Human_SNP_ID_324331346 A-to-I Human chr7 + 66849225 66849225 66849225 TGCCACCATGCCCCACTAATTTTTGTATTTTTAGGTGAGCCAAGGTTTCACGATCTTGGCCAGGC TGCCACCATGCCCCACTAATTTTTGTATTTTTGGGTGAGCCAAGGTTTCACGATCTTGGCCAGGC A G AC027644.1 Ensembl:ENSG00000232546 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1191239912 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16198295 RMVar_hsa_circ_342858,RMVar_hsa_circ_368149 30579 RMVar_ID_30579 Human_SNP_ID_324337511 A-to-I Human chr7 + 66874350 66874350 66874350 GAAATCCTGTCTCTACAAAAAATACAAAAATTAGCTAGGCATGGTGGGGGGTGCCTGTAATACTG GAAATCCTGTCTCTACAAAAAATACAAAAATTGGCTAGGCATGGTGGGGGGTGCCTGTAATACTG A G lnc-TMEM248-4,lnc-TMEM248-4:2 RNACentral:URS00009C4B20,RNACentral:URS00008BD6FF lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1247026160 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7453,RMVar_hsa_circ_342858,RMVar_hsa_circ_31681 30580 RMVar_ID_30580 Human_SNP_ID_324350492 A-to-I Human chr7 + 66927737 66927737 66927737 CCTTGGCCTCCCAAAGTGTTGGGATTACAGGCATGAAACACCATGCCCAGTCTCTCTTTGGTTCC CCTTGGCCTCCCAAAGTGTTGGGATTACAGGCGTGAAACACCATGCCCAGTCTCTCTTTGGTTCC A G TMEM248 Ensembl:ENSG00000106609 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1486502082 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3098522 RMVar_hsa_circ_98577,RMVar_hsa_circ_111417,RMVar_hsa_circ_245391,RMVar_hsa_circ_245392 30581 RMVar_ID_30581 Human_SNP_ID_324350593 A-to-I Human chr7 + 66928108 66928108 66928108 CTGCTGGTGGGCGCCTGTAATCCCATTTAGTCAGGAGTCTGAAGCAGGAGAATCACTCGAACCCA CTGCTGGTGGGCGCCTGTAATCCCATTTAGTCGGGAGTCTGAAGCAGGAGAATCACTCGAACCCA A G TMEM248 Ensembl:ENSG00000106609 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1162180073 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3098524,Human_RBP_ID_8670210,Human_RBP_ID_16198754 RMVar_hsa_circ_98577,RMVar_hsa_circ_111417,RMVar_hsa_circ_245391,RMVar_hsa_circ_245392 30582 RMVar_ID_30582 Human_SNP_ID_324350983 A-to-I Human chr7 + 66929598 66929598 66929598 AGCTGGCATTATAGGCGTGCACCGCCATGCCCAGCTAATTTTTGTATTTTTATTAGAGATGGGGT AGCTGGCATTATAGGCGTGCACCGCCATGCCCGGCTAATTTTTGTATTTTTATTAGAGATGGGGT A G TMEM248 Ensembl:ENSG00000106609 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1233678224 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98577,RMVar_hsa_circ_111417,RMVar_hsa_circ_245391,RMVar_hsa_circ_245392 30583 RMVar_ID_30583 Human_SNP_ID_324351079 A-to-I Human chr7 + 66930017 66930017 66930017 TCCCATCTCTACAAAAAATACAAAAATTAGCCAGGAGTGGTAGCATGCACTTGTAGTCCCAGCTA TCCCATCTCTACAAAAAATACAAAAATTAGCCGGGAGTGGTAGCATGCACTTGTAGTCCCAGCTA A G TMEM248 Ensembl:ENSG00000106609 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs971016653 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98577,RMVar_hsa_circ_111417,RMVar_hsa_circ_245391,RMVar_hsa_circ_245392 30584 RMVar_ID_30584 Human_SNP_ID_324351347 A-to-I Human chr7 + 66931176 66931176 66931176 AATATCAAAATTAGCCGGACGTGGTGATGTGCACCTGTAGTCTCAGCTATTTGGGAGGCTGAGGT AATATCAAAATTAGCCGGACGTGGTGATGTGCGCCTGTAGTCTCAGCTATTTGGGAGGCTGAGGT A G TMEM248 Ensembl:ENSG00000106609 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs894410683 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98577,RMVar_hsa_circ_111417,RMVar_hsa_circ_245391,RMVar_hsa_circ_245392 30585 RMVar_ID_30585 Human_SNP_ID_324351598 A-to-I Human chr7 + 66931930 66931930 66931930 GGATTCATGCCATTCTCCTGCCTCAGCCTCTCAAGTAGCTGGGACTACAGGCGCCCGCCACCACA GGATTCATGCCATTCTCCTGCCTCAGCCTCTCGAGTAGCTGGGACTACAGGCGCCCGCCACCACA A G TMEM248 Ensembl:ENSG00000106609 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1276293790 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98577,RMVar_hsa_circ_111417,RMVar_hsa_circ_245391,RMVar_hsa_circ_245392 30586 RMVar_ID_30586 Human_SNP_ID_324351656 A-to-I Human chr7 + 66932152 66932152 66932152 TAGCTGCTTTCCTCCCCTTATATTAGGTTGGTACAAAAGTAATCGTGGTTTTTGCCATTATGTAT TAGCTGCTTTCCTCCCCTTATATTAGGTTGGTGCAAAAGTAATCGTGGTTTTTGCCATTATGTAT A G TMEM248 Ensembl:ENSG00000106609 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1383289465 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98577,RMVar_hsa_circ_111417,RMVar_hsa_circ_245391,RMVar_hsa_circ_245392 30587 RMVar_ID_30587 Human_SNP_ID_324352325 A-to-I Human chr7 + 66934794 66934794 66934794 AGGTTTTGGGCCAGGTGTGGTGGTTCACACCTATAATCCCAACACTGTGGGAGGCCAGGGTGGGC AGGTTTTGGGCCAGGTGTGGTGGTTCACACCTGTAATCCCAACACTGTGGGAGGCCAGGGTGGGC A G TMEM248 Ensembl:ENSG00000106609 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1224814525 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98577,RMVar_hsa_circ_111417,RMVar_hsa_circ_245391,RMVar_hsa_circ_245392 30588 RMVar_ID_30588 Human_SNP_ID_324375888 A-to-I Human chr7 + 67023226 67023226 67023226 TCAAGCAATTCTCCTGTCTCAGCCTTTGGAGTAGTTGGGACTACAGGCGCATGCCACCACGCTCG TCAAGCAATTCTCCTGTCTCAGCCTTTGGAGTGGTTGGGACTACAGGCGCATGCCACCACGCTCG A G TYW1 Ensembl:ENSG00000198874 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1437352412 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3310,RMVar_hsa_circ_74841,RMVar_hsa_circ_110194,RMVar_hsa_circ_15600,RMVar_hsa_circ_245415,RMVar_hsa_circ_99721,RMVar_hsa_circ_89812,RMVar_hsa_circ_27129,RMVar_hsa_circ_125732,RMVar_hsa_circ_245416,RMVar_hsa_circ_364612,RMVar_hsa_circ_58176,RMVar_hsa_circ_245418,RMVar_hsa_circ_342066,RMVar_hsa_circ_374525,RMVar_hsa_circ_118888,RMVar_hsa_circ_245421,RMVar_hsa_circ_62179,RMVar_hsa_circ_82723,RMVar_hsa_circ_245423,RMVar_hsa_circ_245424,RMVar_hsa_circ_245422,RMVar_hsa_circ_245420 30589 RMVar_ID_30589 Human_SNP_ID_324386181 A-to-I Human chr7 + 67065864 67065864 67065864 AAAACCCTGTATCTACAAAAAATACAAATACTAGCTGGGCGTGGTGCCGCATGCCTATAATCCCA AAAACCCTGTATCTACAAAAAATACAAATACTGGCTGGGCGTGGTGCCGCATGCCTATAATCCCA A G TYW1 Ensembl:ENSG00000198874 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1333540362 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110194,RMVar_hsa_circ_15600,RMVar_hsa_circ_245415,RMVar_hsa_circ_67675,RMVar_hsa_circ_89812,RMVar_hsa_circ_125732,RMVar_hsa_circ_58176,RMVar_hsa_circ_245418,RMVar_hsa_circ_374525,RMVar_hsa_circ_118888,RMVar_hsa_circ_245423,RMVar_hsa_circ_245424,RMVar_hsa_circ_245422,RMVar_hsa_circ_356722,RMVar_hsa_circ_377600,RMVar_hsa_circ_70891,RMVar_hsa_circ_110316,RMVar_hsa_circ_245425,RMVar_hsa_circ_365403,RMVar_hsa_circ_366292,RMVar_hsa_circ_301414,RMVar_hsa_circ_339783,RMVar_hsa_circ_245426,RMVar_hsa_circ_306800,RMVar_hsa_circ_296037,RMVar_hsa_circ_245428,RMVar_hsa_circ_245429,RMVar_hsa_circ_245427 30590 RMVar_ID_30590 Human_SNP_ID_324427989 A-to-I Human chr7 - 67243942 67243941 67243942 AGGCGTGGTGGCGGGTGCCTGTGGTCCCAGCTACTGGGGAGGCTGAGGCAGGACAATGACGTGAA AGGCGTGGTGGCGGGTGCCTGTGGTCCCAGCT_CTGGGGAGGCTGAGGCAGGACAATGACGTGAA GT G RF00017-1020 RNACentral:URS000099BA6B SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1176801438 Functional Loss DEL dbSNP153 33..33 33 - - - 30591 RMVar_ID_30591 Human_SNP_ID_324429981 A-to-I Human chr7 - 67252730 67252730 67252730 TGCCACCATATCTGGTTACTTTCGTATTTTTAATACAGACAGGGTTTCACCATCTTGGCCAGGCT TGCCACCATATCTGGTTACTTTCGTATTTTTAGTACAGACAGGGTTTCACCATCTTGGCCAGGCT T C RF00017-1020 RNACentral:URS000099BA6B SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285627879 Functional Loss SNV dbSNP153 33..33 33 - - - 30592 RMVar_ID_30592 Human_SNP_ID_324434139 A-to-I Human chr7 - 67269457 67269457 67269457 ACAATCTCGGCTCACTGCAACTTCTTCCTCCCAGATTCAAGTGATTCCCCTGCCTCAGCCTCCCA ACAATCTCGGCTCACTGCAACTTCTTCCTCCCTGATTCAAGTGATTCCCCTGCCTCAGCCTCCCA T A RF00017-1020 RNACentral:URS000099BA6B SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs549489947 Functional Loss SNV dbSNP153 33..33 33 - - - 30593 RMVar_ID_30593 Human_SNP_ID_324434746 A-to-I Human chr7 - 67271797 67271797 67271797 AGAATGCAATGGCATGATCTTGGGTCACTGCAACCTCCGCCTCGTGGGTTCAAGCAATTCTCCTG AGAATGCAATGGCATGATCTTGGGTCACTGCAGCCTCCGCCTCGTGGGTTCAAGCAATTCTCCTG T C RF00017-1020 RNACentral:URS000099BA6B SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909337132 Functional Loss SNV dbSNP153 33..33 33 - - - 30594 RMVar_ID_30594 Human_SNP_ID_324434747 A-to-I Human chr7 - 67271797 67271797 67271797 AGAATGCAATGGCATGATCTTGGGTCACTGCAACCTCCGCCTCGTGGGTTCAAGCAATTCTCCTG AGAATGCAATGGCATGATCTTGGGTCACTGCACCCTCCGCCTCGTGGGTTCAAGCAATTCTCCTG T G RF00017-1020 RNACentral:URS000099BA6B SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909337132 Functional Loss SNV dbSNP153 33..33 33 - - - 30595 RMVar_ID_30595 Human_SNP_ID_324435343 A-to-I Human chr7 - 67274189 67274189 67274189 ATCGAAAGAAGAAGTTTGAGTCCAGCCTGGCCAGTATGGCGAAACTCTGTCTCTACTAAAATACA ATCGAAAGAAGAAGTTTGAGTCCAGCCTGGCCGGTATGGCGAAACTCTGTCTCTACTAAAATACA T C RF00017-1020,lnc-SBDS-28 RNACentral:URS000099BA6B,RNACentral:URS0000D5BE91 SRP RNA,lincRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs574696055 Functional Loss SNV dbSNP153 33..33 33 - - - 30596 RMVar_ID_30596 Human_SNP_ID_324435757 A-to-I Human chr7 - 67276142 67276141 67276142 GGCCAGACACAGTGGTCAGTCCTGCAATCCCAACACTTTGGTTGGCTAAGGTGGGAGGATTTCTT GGCCAGACACAGTGGTCAGTCCTGCAATCCCA_CACTTTGGTTGGCTAAGGTGGGAGGATTTCTT GT G RF00017-1020,lnc-SBDS-29 RNACentral:URS000099BA6B,RNACentral:URS0000D5E0F8 SRP RNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs58152480 Functional Loss DEL dbSNP153 33..33 33 - - - 30597 RMVar_ID_30597 Human_SNP_ID_324438025 A-to-I Human chr7 - 67285284 67285284 67285284 TTGAGCCCAGGATATGGAGGCTGTGGTGAGCTATGATCTCACCACTGCACTCTAGCTTGGGGGAC TTGAGCCCAGGATATGGAGGCTGTGGTGAGCTGTGATCTCACCACTGCACTCTAGCTTGGGGGAC T C RF00017-1020 RNACentral:URS000099BA6B SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1287301746 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26112140 30598 RMVar_ID_30598 Human_SNP_ID_324443195 A-to-I Human chr7 - 67304085 67304085 67304085 GTGGTGGCGTGCACCTGTAATCCAAGCTACTCAGGAGGCTGAGATGGGAGAACTGCTTGAACCCG GTGGTGGCGTGCACCTGTAATCCAAGCTACTCGGGAGGCTGAGATGGGAGAACTGCTTGAACCCG T C RF00017-1020 RNACentral:URS000099BA6B SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs374389376 Functional Loss SNV dbSNP153 33..33 33 - - - 30599 RMVar_ID_30599 Human_SNP_ID_324445389 A-to-I Human chr7 + 67312617 67312617 67312617 CAGAGGTTGCAGTGAGCCAAGATCACACCACTACACTCTAGCCTGCGCTACAGAGCAAGACTCCA CAGAGGTTGCAGTGAGCCAAGATCACACCACTGCACTCTAGCCTGCGCTACAGAGCAAGACTCCA A G STAG3L4 Ensembl:ENSG00000106610 Pseudogene intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1156794166 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17577426 30600 RMVar_ID_30600 Human_SNP_ID_324445543 A-to-I Human chr7 + 67313037 67313037 67313037 TAGAGGCAGGGTCTCACTATGCTGCCCAGGCTAGTCTTGAACTCCTGGGCTTAATCAGTCCTCCC TAGAGGCAGGGTCTCACTATGCTGCCCAGGCTTGTCTTGAACTCCTGGGCTTAATCAGTCCTCCC A T STAG3L4 Ensembl:ENSG00000106610 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1450800132 Functional Loss SNV dbSNP153 33..33 33 - - - 30601 RMVar_ID_30601 Human_SNP_ID_324445551 A-to-I Human chr7 + 67313085 67313085 67313085 GCTTAATCAGTCCTCCCACCTCAGCCTCCCAAAAAGTTGGGATTGTAGGCATGAGCCACCATGCC GCTTAATCAGTCCTCCCACCTCAGCCTCCCAAGAAGTTGGGATTGTAGGCATGAGCCACCATGCC A G STAG3L4 Ensembl:ENSG00000106610 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1208507910 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17577767 30602 RMVar_ID_30602 Human_SNP_ID_324446338 A-to-I Human chr7 + 67315725 67315725 67315725 TTTTAGTAGAGATGACGGGGTTTCACCATGTTAGCCAGGATGGTCTCAATCTGACCTTGTGATCC TTTTAGTAGAGATGACGGGGTTTCACCATGTTCGCCAGGATGGTCTCAATCTGACCTTGTGATCC A C STAG3L4 Ensembl:ENSG00000106610 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs369543716 Functional Loss SNV dbSNP153 33..33 33 - - - 30603 RMVar_ID_30603 Human_SNP_ID_324446339 A-to-I Human chr7 + 67315725 67315725 67315725 TTTTAGTAGAGATGACGGGGTTTCACCATGTTAGCCAGGATGGTCTCAATCTGACCTTGTGATCC TTTTAGTAGAGATGACGGGGTTTCACCATGTTGGCCAGGATGGTCTCAATCTGACCTTGTGATCC A G STAG3L4 Ensembl:ENSG00000106610 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs369543716 Functional Loss SNV dbSNP153 33..33 33 - - - 30604 RMVar_ID_30604 Human_SNP_ID_324446562 A-to-I Human chr7 + 67316157 67316157 67316157 CGGGGAAGCAGAGGTTGCAGTGAGCCGAGATCACGCCATTGCACTCCAGCCTGGGCAACTAGACT CGGGGAAGCAGAGGTTGCAGTGAGCCGAGATCGCGCCATTGCACTCCAGCCTGGGCAACTAGACT A G STAG3L4 Ensembl:ENSG00000106610 Pseudogene intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs776005469 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16200322,Human_RBP_ID_23315530,Human_RBP_ID_26138685 30605 RMVar_ID_30605 Human_SNP_ID_324446972 A-to-I Human chr7 + 67317705 67317705 67317705 TCTGGAGGCTGGGCGAGGTGGCTCACTCTGGTAATCCCAGCAGTTTGGGAGGCTGAGGCAGGAGG TCTGGAGGCTGGGCGAGGTGGCTCACTCTGGTGATCCCAGCAGTTTGGGAGGCTGAGGCAGGAGG A G STAG3L4 Ensembl:ENSG00000106610 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1048388359 Functional Loss SNV dbSNP153 33..33 33 - - - 30606 RMVar_ID_30606 Human_SNP_ID_324447486 A-to-I Human chr7 + 67319438 67319438 67319438 TTTTGTATTTTTAGTAGAGATGGCGTTTCACCATGTTAGCCAGGCTGGTCTCAATCTCCTGACCT TTTTGTATTTTTAGTAGAGATGGCGTTTCACCGTGTTAGCCAGGCTGGTCTCAATCTCCTGACCT A G STAG3L4 Ensembl:ENSG00000106610 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs764478479 Functional Loss SNV dbSNP153 33..33 33 - - - 30607 RMVar_ID_30607 Human_SNP_ID_324447488 A-to-I Human chr7 + 67319443 67319443 67319443 TATTTTTAGTAGAGATGGCGTTTCACCATGTTAGCCAGGCTGGTCTCAATCTCCTGACCTCAGGT TATTTTTAGTAGAGATGGCGTTTCACCATGTTGGCCAGGCTGGTCTCAATCTCCTGACCTCAGGT A G STAG3L4 Ensembl:ENSG00000106610 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1454050569 Functional Loss SNV dbSNP153 33..33 33 - - - 30608 RMVar_ID_30608 Human_SNP_ID_324451826 A-to-I Human chr7 + 67339801 67339801 67339801 TTCGGCTAATTTTAATTTTTTTTTGTAGAGACAGGGTCTTGTTCTATTGTCCAAGCTGGTCTTGA TTCGGCTAATTTTAATTTTTTTTTGTAGAGACGGGGTCTTGTTCTATTGTCCAAGCTGGTCTTGA A G STAG3L4 Ensembl:ENSG00000106610 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs948102481 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_871958,Human_Splice_Rec_871959,Human_Splice_Rec_871970 30609 RMVar_ID_30609 Human_SNP_ID_324452333 A-to-I Human chr7 + 67341773 67341773 67341773 GGGTGTGTTGGCAGGAGCCTGTAATCCCAGCTACTTGGGGGACTGAGGCAGGAGAATTGCCTGAA GGGTGTGTTGGCAGGAGCCTGTAATCCCAGCTGCTTGGGGGACTGAGGCAGGAGAATTGCCTGAA A G STAG3L4 Ensembl:ENSG00000106610 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1266435282 Functional Loss SNV dbSNP153 33..33 33 - - - 30610 RMVar_ID_30610 Human_SNP_ID_325071518 A-to-I Human chr7 + 69666718 69666718 69666718 GAGCTCAGGAGTTCCAGACCAGCCTAGGCAACATAGCAAGACTCCCATCTTGACAAAAAATAAAA GAGCTCAGGAGTTCCAGACCAGCCTAGGCAACGTAGCAAGACTCCCATCTTGACAAAAAATAAAA A G AUTS2 Ensembl:ENSG00000158321 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs951555407 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_245450,RMVar_hsa_circ_123657 30611 RMVar_ID_30611 Human_SNP_ID_325334608 A-to-I Human chr7 + 70784151 70784151 70784151 TAAGATTTTCAGTGCCCCAAAACATAAGAATCAACCAGCTTTTCCTGGCATTGAAAGTTGAGAGA TAAGATTTTCAGTGCCCCAAAACATAAGAATCTACCAGCTTTTCCTGGCATTGAAAGTTGAGAGA A T AUTS2 Ensembl:ENSG00000158321 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs993335601 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119594,RMVar_hsa_circ_245462,RMVar_hsa_circ_7987,RMVar_hsa_circ_49339,RMVar_hsa_circ_9813 30612 RMVar_ID_30612 Human_SNP_ID_325510734 A-to-I Human chr7 + 71466551 71466551 71466551 GCTGTTTCTTGTGGGGGAAATTTGCATTCTGTAGAGAATTCCCTTCCCTTCCTAGGTCTTTCCTG GCTGTTTCTTGTGGGGGAAATTTGCATTCTGTGGAGAATTCCCTTCCCTTCCTAGGTCTTTCCTG A G GALNT17 Ensembl:ENSG00000185274 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1357204270 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10927 30613 RMVar_ID_30613 Human_SNP_ID_325570006 A-to-I Human chr7 + 71697913 71697913 71697913 GGGAGGCCTAGTCAGGCAGATCACCTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGGCAA GGGAGGCCTAGTCAGGCAGATCACCTGAGGTCGGGAGTTCAAGACCAGCCTGGCCAACATGGCAA A G GALNT17 Ensembl:ENSG00000185274 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1434638462 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82918,RMVar_hsa_circ_245506,RMVar_hsa_circ_88756,RMVar_hsa_circ_245509,RMVar_hsa_circ_245510 30614 RMVar_ID_30614 Human_SNP_ID_325570016 A-to-I Human chr7 + 71697984 71697984 71697984 GTCTCTACTAAAAGTACAAACATTAGCCAGGCATGGTGGTGGGCGCCTGTAATCCCAGCTACTCA GTCTCTACTAAAAGTACAAACATTAGCCAGGCTTGGTGGTGGGCGCCTGTAATCCCAGCTACTCA A T GALNT17 Ensembl:ENSG00000185274 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs541182823 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82918,RMVar_hsa_circ_245506,RMVar_hsa_circ_88756,RMVar_hsa_circ_245509,RMVar_hsa_circ_245510 30615 RMVar_ID_30615 Human_SNP_ID_325570022 A-to-I Human chr7 + 71698012 71698012 71698012 AGGCATGGTGGTGGGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAA AGGCATGGTGGTGGGCGCCTGTAATCCCAGCTGCTCAGGAGGCTGAGGCAGGAGAATTGCTTGAA A G GALNT17 Ensembl:ENSG00000185274 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs866096798 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82918,RMVar_hsa_circ_245506,RMVar_hsa_circ_88756,RMVar_hsa_circ_245509,RMVar_hsa_circ_245510 30616 RMVar_ID_30616 Human_SNP_ID_325570025 A-to-I Human chr7 + 71698016 71698016 71698016 ATGGTGGTGGGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAATCTG ATGGTGGTGGGCGCCTGTAATCCCAGCTACTCCGGAGGCTGAGGCAGGAGAATTGCTTGAATCTG A C GALNT17 Ensembl:ENSG00000185274 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs754577891 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82918,RMVar_hsa_circ_245506,RMVar_hsa_circ_88756,RMVar_hsa_circ_245509,RMVar_hsa_circ_245510 30617 RMVar_ID_30617 Human_SNP_ID_325570026 A-to-I Human chr7 + 71698016 71698016 71698016 ATGGTGGTGGGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAATCTG ATGGTGGTGGGCGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCTTGAATCTG A G GALNT17 Ensembl:ENSG00000185274 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs754577891 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82918,RMVar_hsa_circ_245506,RMVar_hsa_circ_88756,RMVar_hsa_circ_245509,RMVar_hsa_circ_245510 30618 RMVar_ID_30618 Human_SNP_ID_325622906 A-to-I Human chr7 - 71890803 71890796 71890804 AGTTTCCGGCTGCAGTGAGCCATAACTGCACCACTGCACTCCAGTCTGGGCAACAGAGTAAGACA AGTTTCCGGCTGCAGTGAGCCATAACTGCAC________TCCAGTCTGGGCAACAGAGTAAGACA AGTGCAGTG A CALN1 Ensembl:ENSG00000183166 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1401353502 Functional Loss DEL dbSNP153 32..39 33 - - - RMVar_hsa_circ_107352,RMVar_hsa_circ_245511 30619 RMVar_ID_30619 Human_SNP_ID_325624331 A-to-I Human chr7 - 71896451 71896451 71896451 AACTGGGAACTGTTGCATCAGGCCTTGTAAGCATGATTCCATTTTAACCTGCTCAGCTATTTTTT AACTGGGAACTGTTGCATCAGGCCTTGTAAGCGTGATTCCATTTTAACCTGCTCAGCTATTTTTT T C CALN1 Ensembl:ENSG00000183166 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs567991072 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107352,RMVar_hsa_circ_245511 30620 RMVar_ID_30620 Human_SNP_ID_325624499 A-to-I Human chr7 - 71897192 71897192 71897192 ATTAAATGCGAATCTTACAGGAATTCACAACGAAAGGCCTGTGATGCTGGACTCACAGATATTAC ATTAAATGCGAATCTTACAGGAATTCACAACGGAAGGCCTGTGATGCTGGACTCACAGATATTAC T C CALN1 Ensembl:ENSG00000183166 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1322543011 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107352,RMVar_hsa_circ_245511 30621 RMVar_ID_30621 Human_SNP_ID_325643485 A-to-I Human chr7 - 71966740 71966740 71966740 TTGCTCCCCAAAACGTTAAGAACCATGGTATTAGTCTGTTCTTGTATTGCTGTAAATACCTGAGA TTGCTCCCCAAAACGTTAAGAACCATGGTATTCGTCTGTTCTTGTATTGCTGTAAATACCTGAGA T G CALN1 Ensembl:ENSG00000183166 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1282539221 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107352,RMVar_hsa_circ_245511 30622 RMVar_ID_30622 Human_SNP_ID_325644367 A-to-I Human chr7 - 71970121 71970121 71970121 TGCTGGGCCGGGCGTGGTGGCTCATGCCTGTAATCCTAGCACTTTCGGAGGCCAAGGCAGGAGGA TGCTGGGCCGGGCGTGGTGGCTCATGCCTGTATTCCTAGCACTTTCGGAGGCCAAGGCAGGAGGA T A CALN1 Ensembl:ENSG00000183166 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1034293426 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107352,RMVar_hsa_circ_245511 30623 RMVar_ID_30623 Human_SNP_ID_325663683 A-to-I Human chr7 - 72040218 72040218 72040218 CTCCTGCCTCAGCCTCTGAAAGTGATGAGATTACAAGCATGAACCACCCATGCCCAGCCTCATAA CTCCTGCCTCAGCCTCTGAAAGTGATGAGATTGCAAGCATGAACCACCCATGCCCAGCCTCATAA T C CALN1 Ensembl:ENSG00000183166 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs188972508 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107352,RMVar_hsa_circ_245512,RMVar_hsa_circ_80448,RMVar_hsa_circ_378643,RMVar_hsa_circ_245511,RMVar_hsa_circ_375684,RMVar_hsa_circ_245513 30624 RMVar_ID_30624 Human_SNP_ID_325733749 A-to-I Human chr7 - 72273592 72273592 72273592 ATCGCCTGAGCCCAGGAGTTTGAGGCTACTGTAAGCTATGATTGTACTACTGCACTTGCACTTGA ATCGCCTGAGCCCAGGAGTTTGAGGCTACTGTGAGCTATGATTGTACTACTGCACTTGCACTTGA T C CALN1 Ensembl:ENSG00000183166 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs948038995 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107352,RMVar_hsa_circ_245512,RMVar_hsa_circ_80448,RMVar_hsa_circ_245511,RMVar_hsa_circ_375684,RMVar_hsa_circ_245513,RMVar_hsa_circ_377790 30625 RMVar_ID_30625 Human_SNP_ID_325770824 A-to-I Human chr7 - 72380626 72380624 72380626 TGAGCAGCCGTCTAGCTGGTTTCTCTCTTAATATGACTCTGATGCTAGGACATGAAGCTTGCAGG TGAGCAGCCGTCTAGCTGGTTTCTCTCTTAAT__GACTCTGATGCTAGGACATGAAGCTTGCAGG CAT C CALN1 Ensembl:ENSG00000183166 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1562934525 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_245512,RMVar_hsa_circ_80448,RMVar_hsa_circ_319972,RMVar_hsa_circ_245518 30626 RMVar_ID_30626 Human_SNP_ID_325770825 A-to-I Human chr7 - 72380626 72380626 72380626 TGAGCAGCCGTCTAGCTGGTTTCTCTCTTAATATGACTCTGATGCTAGGACATGAAGCTTGCAGG TGAGCAGCCGTCTAGCTGGTTTCTCTCTTAATGTGACTCTGATGCTAGGACATGAAGCTTGCAGG T C CALN1 Ensembl:ENSG00000183166 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs530295081 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_245512,RMVar_hsa_circ_80448,RMVar_hsa_circ_319972,RMVar_hsa_circ_245518 30627 RMVar_ID_30627 Human_SNP_ID_325886370 A-to-I Human chr7 - 72822942 72822942 72822942 TCACCCAAGCTGGAGTGCAGTGGCATGATTTTAGTTCACTGCAGCCTCGACCTCTTGGGCTTCAG TCACCCAAGCTGGAGTGCAGTGGCATGATTTTGGTTCACTGCAGCCTCGACCTCTTGGGCTTCAG T C RN7SL377P,TYW1B Ensembl:ENSG00000266569,Ensembl:ENSG00000277149 Other,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs549413995 Functional Loss SNV dbSNP153 33..33 33 - - - 30628 RMVar_ID_30628 Human_SNP_ID_325889175 A-to-I Human chr7 + 72833298 72833298 72833298 CCCCTTTTTATTCTCGCTCTGTCACCCAGACTAGAGTGCAGTGGCGCGATCTCGGCTCATTGCAA CCCCTTTTTATTCTCGCTCTGTCACCCAGACTGGAGTGCAGTGGCGCGATCTCGGCTCATTGCAA A G SBDSP1 Ensembl:ENSG00000225648 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs572600170 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_301588,RMVar_hsa_circ_323121 30629 RMVar_ID_30629 Human_SNP_ID_325889639 A-to-I Human chr7 + 72834903 72834903 72834903 AACCCTGTCTCTACTAAAAATACAAAATAGTCAGGCGTGGTGGCACATCCCTGTAATCCCAGCTA AACCCTGTCTCTACTAAAAATACAAAATAGTCTGGCGTGGTGGCACATCCCTGTAATCCCAGCTA A T SBDSP1 Ensembl:ENSG00000225648 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1554483261 Functional Loss SNV dbSNP153 33..33 33 - - - 30630 RMVar_ID_30630 Human_SNP_ID_325889780 A-to-I Human chr7 + 72835565 72835564 72835566 TGAGACAGAGTTTCACTCTCGTTGCCCAGGCTAGAGTGCAATGGTGTGATCTCAGCTCACTGCAA TGAGACAGAGTTTCACTCTCGTTGCCCAGGCT__AGTGCAATGGTGTGATCTCAGCTCACTGCAA TAG T SBDSP1 Ensembl:ENSG00000225648 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1420042547 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_17429074 30631 RMVar_ID_30631 Human_SNP_ID_325904946 A-to-I Human chr7 + 72894723 72894723 72894723 CCTGTCGCCCAGGCTGGGAGTGCGGAGGTGCTATCATGGCTTACTGCAGCCTCCAACTCCTGGAC CCTGTCGCCCAGGCTGGGAGTGCGGAGGTGCTGTCATGGCTTACTGCAGCCTCCAACTCCTGGAC A G POM121 Ensembl:ENSG00000196313 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1401487462 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_309570,RMVar_hsa_circ_312976 30632 RMVar_ID_30632 Human_SNP_ID_325904953 A-to-I Human chr7 + 72894758 72894757 72894759 ATGGCTTACTGCAGCCTCCAACTCCTGGACTCAAGAGATCCTCCACCCCACCTTCCAAGTAGCTG ATGGCTTACTGCAGCCTCCAACTCCTGGACTC__GAGATCCTCCACCCCACCTTCCAAGTAGCTG CAA C POM121 Ensembl:ENSG00000196313 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1486330030 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_253828 RMVar_hsa_circ_309570,RMVar_hsa_circ_312976 30633 RMVar_ID_30633 Human_SNP_ID_325904967 A-to-I Human chr7 + 72894798 72894798 72894798 CTCCACCCCACCTTCCAAGTAGCTGGCACTACAGGTGCGCACAGCTGACCATGCCTGGCTAATTT CTCCACCCCACCTTCCAAGTAGCTGGCACTACCGGTGCGCACAGCTGACCATGCCTGGCTAATTT A C POM121 Ensembl:ENSG00000196313 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1269672750 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_309570,RMVar_hsa_circ_312976 30634 RMVar_ID_30634 Human_SNP_ID_325904968 A-to-I Human chr7 + 72894798 72894798 72894798 CTCCACCCCACCTTCCAAGTAGCTGGCACTACAGGTGCGCACAGCTGACCATGCCTGGCTAATTT CTCCACCCCACCTTCCAAGTAGCTGGCACTACGGGTGCGCACAGCTGACCATGCCTGGCTAATTT A G POM121 Ensembl:ENSG00000196313 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1269672750 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_309570,RMVar_hsa_circ_312976 30635 RMVar_ID_30635 Human_SNP_ID_325904982 A-to-I Human chr7 + 72894845 72894845 72894845 ACCATGCCTGGCTAATTTTAAAAGTTTTAGGTAAAAATGGGGTGTCCCTATGTTGCCCAGGCTGG ACCATGCCTGGCTAATTTTAAAAGTTTTAGGTGAAAATGGGGTGTCCCTATGTTGCCCAGGCTGG A G POM121 Ensembl:ENSG00000196313 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs553453707 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17577430,Human_RBP_ID_22483513,Human_RBP_ID_24225219 RMVar_hsa_circ_309570,RMVar_hsa_circ_312976 30636 RMVar_ID_30636 Human_SNP_ID_325905627 A-to-I Human chr7 + 72897872 72897872 72897872 GCAAGACTCTGTCTCTAAAAAAATAAAAAATTAGCTGGGTTTGGTGGTGCGTGCCTGTAGTCCCA GCAAGACTCTGTCTCTAAAAAAATAAAAAATTTGCTGGGTTTGGTGGTGCGTGCCTGTAGTCCCA A T POM121 Ensembl:ENSG00000196313 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1446870278 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_309570,RMVar_hsa_circ_312976 30637 RMVar_ID_30637 Human_SNP_ID_325905720 A-to-I Human chr7 + 72898294 72898294 72898294 TTTGAAAATAAATAGACAGATGGAGTCTCACTAAGTTGCCCAGGCTGGTCTCAAACTCCTGGGCT TTTGAAAATAAATAGACAGATGGAGTCTCACTGAGTTGCCCAGGCTGGTCTCAAACTCCTGGGCT A G POM121 Ensembl:ENSG00000196313 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs542450195 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_309570,RMVar_hsa_circ_312976 30638 RMVar_ID_30638 Human_SNP_ID_325905790 A-to-I Human chr7 + 72898619 72898619 72898619 GGGAGTGTGAGCCCAGCCTGGCCAACATGGCGAAATCCTGTCTCTACTAAAAATACAAAAAATTA GGGAGTGTGAGCCCAGCCTGGCCAACATGGCGTAATCCTGTCTCTACTAAAAATACAAAAAATTA A T POM121 Ensembl:ENSG00000196313 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1554492085 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_309570,RMVar_hsa_circ_312976 30639 RMVar_ID_30639 Human_SNP_ID_325905977 A-to-I Human chr7 + 72899165 72899165 72899165 CCACTACACCTGGCTAATTTTTTTGTATTTTTAGTAGAGATGGGGTTTCATCATGTTGGTCAGGC CCACTACACCTGGCTAATTTTTTTGTATTTTTGGTAGAGATGGGGTTTCATCATGTTGGTCAGGC A G POM121 Ensembl:ENSG00000196313 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1307048211 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_309570,RMVar_hsa_circ_312976 30640 RMVar_ID_30640 Human_SNP_ID_325906595 A-to-I Human chr7 + 72901535 72901535 72901535 CGCCACCGTGCCTGGCTAATTTTTGTCTTTTCAGTAGAGACGGAGTTTCACCATTTTGGCTAGGC CGCCACCGTGCCTGGCTAATTTTTGTCTTTTCGGTAGAGACGGAGTTTCACCATTTTGGCTAGGC A G POM121 Ensembl:ENSG00000196313 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1281741130 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_309570,RMVar_hsa_circ_312976 30641 RMVar_ID_30641 Human_SNP_ID_325906807 A-to-I Human chr7 + 72902402 72902402 72902402 CTCCTGTCTCAGCCTCCTGAGTAGCTGGGATTATAGGCACCCACCACCATGCCTGGCTAATTTTT CTCCTGTCTCAGCCTCCTGAGTAGCTGGGATTGTAGGCACCCACCACCATGCCTGGCTAATTTTT A G POM121 Ensembl:ENSG00000196313 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1281068428 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_309570,RMVar_hsa_circ_312976 30642 RMVar_ID_30642 Human_SNP_ID_325907041 A-to-I Human chr7 + 72903314 72903314 72903314 CAAAACTTAGCCGGACATGGTGGTATGCGCCTATAATCCCAGCTATTTGGGAGGTTAAGGAAGAG CAAAACTTAGCCGGACATGGTGGTATGCGCCTGTAATCCCAGCTATTTGGGAGGTTAAGGAAGAG A G POM121 Ensembl:ENSG00000196313 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1172731908 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23198413 RMVar_hsa_circ_309570,RMVar_hsa_circ_312976 30643 RMVar_ID_30643 Human_SNP_ID_325907051 A-to-I Human chr7 + 72903369 72903369 72903369 TAAGGAAGAGGAACTGCTTGAACCAGGGAGGTAGAGGTTGCAATGAGTGGAGATCACACCACTGC TAAGGAAGAGGAACTGCTTGAACCAGGGAGGTGGAGGTTGCAATGAGTGGAGATCACACCACTGC A G POM121 Ensembl:ENSG00000196313 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1279612055 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16209808 RMVar_hsa_circ_309570,RMVar_hsa_circ_312976 30644 RMVar_ID_30644 Human_SNP_ID_325910742 A-to-I Human chr7 + 72920516 72920516 72920516 GACTACAGGCACCAGTCACCATCACCACGCCCAGCTGATTTTTTGTATTTTTAGTAGAGACGGGG GACTACAGGCACCAGTCACCATCACCACGCCCGGCTGATTTTTTGTATTTTTAGTAGAGACGGGG A G POM121 Ensembl:ENSG00000196313 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1329211364 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_312976 30645 RMVar_ID_30645 Human_SNP_ID_325910749 A-to-I Human chr7 + 72920536 72920536 72920536 ATCACCACGCCCAGCTGATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTAGCCAGGA ATCACCACGCCCAGCTGATTTTTTGTATTTTTGGTAGAGACGGGGTTTCACCATGTTAGCCAGGA A G POM121 Ensembl:ENSG00000196313 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1397687912 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_312976 30646 RMVar_ID_30646 Human_SNP_ID_325913512 A-to-I Human chr7 + 72930186 72930186 72930186 GCGTTCATTCATTGACTAGGGCCAGACATGGTAGCTTAGCCATGTAATCCCAGCACTTTGGAAGG GCGTTCATTCATTGACTAGGGCCAGACATGGTGGCTTAGCCATGTAATCCCAGCACTTTGGAAGG A G POM121 Ensembl:ENSG00000196313 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1400228860 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16210426,Human_RBP_ID_19138915,Human_RBP_ID_22367255 RMVar_hsa_circ_351656 30647 RMVar_ID_30647 Human_SNP_ID_325926235 A-to-I Human chr7 - 72982043 72982043 72982043 TTATTTATTTTTAGTAGAGATGGGGTTTTGCCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCT TTATTTATTTTTAGTAGAGATGGGGTTTTGCCGTGTTGGCCAGGCTGGTCTCGAACTCCTGACCT T C STAG3L3 Ensembl:ENSG00000174353 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417532520 Functional Loss SNV dbSNP153 33..33 33 - - - 30648 RMVar_ID_30648 Human_SNP_ID_325928821 A-to-I Human chr7 - 72995547 72995547 72995547 GCCTTAAGCAATCCTCCTACTTCAGCCTCCCAAAGTGCTGAGATTATAGGTGTGAGCCACTGCAC GCCTTAAGCAATCCTCCTACTTCAGCCTCCCAGAGTGCTGAGATTATAGGTGTGAGCCACTGCAC T C STAG3L3 Ensembl:ENSG00000174353 Pseudogene intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1369142746 Functional Loss SNV dbSNP153 33..33 33 - - - 30649 RMVar_ID_30649 Human_SNP_ID_325928826 A-to-I Human chr7 - 72995561 72995561 72995561 GCCTCAAACTCCTGGCCTTAAGCAATCCTCCTACTTCAGCCTCCCAAAGTGCTGAGATTATAGGT GCCTCAAACTCCTGGCCTTAAGCAATCCTCCTTCTTCAGCCTCCCAAAGTGCTGAGATTATAGGT T A STAG3L3 Ensembl:ENSG00000174353 Pseudogene intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1392272578 Functional Loss SNV dbSNP153 33..33 33 - - - 30650 RMVar_ID_30650 Human_SNP_ID_325928827 A-to-I Human chr7 - 72995561 72995561 72995561 GCCTCAAACTCCTGGCCTTAAGCAATCCTCCTACTTCAGCCTCCCAAAGTGCTGAGATTATAGGT GCCTCAAACTCCTGGCCTTAAGCAATCCTCCTCCTTCAGCCTCCCAAAGTGCTGAGATTATAGGT T G STAG3L3 Ensembl:ENSG00000174353 Pseudogene intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1392272578 Functional Loss SNV dbSNP153 33..33 33 - - - 30651 RMVar_ID_30651 Human_SNP_ID_326015645 A-to-I Human chr7 - 73455166 73455166 73455166 AGCCTTAAGTTCAGGACCAGGTGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAG AGCCTTAAGTTCAGGACCAGGTGCGGTGGCTCGCGCCTGTAATCCCAGCACTTTGGGAGGCTGAG T C BAZ1B Ensembl:ENSG00000009954 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1016200462 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16211401 RMVar_hsa_circ_1418,RMVar_hsa_circ_87909,RMVar_hsa_circ_98461,RMVar_hsa_circ_67704,RMVar_hsa_circ_306295,RMVar_hsa_circ_74266,RMVar_hsa_circ_245552,RMVar_hsa_circ_245553,RMVar_hsa_circ_99589,RMVar_hsa_circ_319221,RMVar_hsa_circ_350508,RMVar_hsa_circ_74779,RMVar_hsa_circ_245554,RMVar_hsa_circ_245555,RMVar_hsa_circ_325430,RMVar_hsa_circ_338640,RMVar_hsa_circ_318930,RMVar_hsa_circ_15416,RMVar_hsa_circ_289645,RMVar_hsa_circ_245556,RMVar_hsa_circ_372776,RMVar_hsa_circ_49126,RMVar_hsa_circ_245557,RMVar_hsa_circ_245558 30652 RMVar_ID_30652 Human_SNP_ID_326017300 A-to-I Human chr7 - 73461175 73461175 73461175 GGTTGGGAGTTCGAGACCAGTCTGACCAGCATAGAGAAACCCCGTCTCTACTAAAAATACAAAAA GGTTGGGAGTTCGAGACCAGTCTGACCAGCATGGAGAAACCCCGTCTCTACTAAAAATACAAAAA T C BAZ1B Ensembl:ENSG00000009954 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1407343836 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16211570 RMVar_hsa_circ_59672,RMVar_hsa_circ_1418,RMVar_hsa_circ_87909,RMVar_hsa_circ_98461,RMVar_hsa_circ_306295,RMVar_hsa_circ_74266,RMVar_hsa_circ_245552,RMVar_hsa_circ_245553,RMVar_hsa_circ_99589,RMVar_hsa_circ_319221,RMVar_hsa_circ_74779,RMVar_hsa_circ_245554,RMVar_hsa_circ_245555,RMVar_hsa_circ_325430,RMVar_hsa_circ_318930,RMVar_hsa_circ_15416,RMVar_hsa_circ_372776,RMVar_hsa_circ_49126,RMVar_hsa_circ_245558,RMVar_hsa_circ_293924,RMVar_hsa_circ_371252,RMVar_hsa_circ_378325,RMVar_hsa_circ_307773,RMVar_hsa_circ_292795,RMVar_hsa_circ_70156,RMVar_hsa_circ_273435,RMVar_hsa_circ_69359,RMVar_hsa_circ_245561,RMVar_hsa_circ_245563,RMVar_hsa_circ_245564,RMVar_hsa_circ_245562,RMVar_hsa_circ_245560 30653 RMVar_ID_30653 Human_SNP_ID_326017316 A-to-I Human chr7 - 73461235 73461235 73461235 GCGGTGGCTTACGCCTGTAATCCCAGCACTTTAGGAGGCCAAGGTGGGCAGATCACTTGAGGTTG GCGGTGGCTTACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGCAGATCACTTGAGGTTG T C BAZ1B Ensembl:ENSG00000009954 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1246326750 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26115631 RMVar_hsa_circ_59672,RMVar_hsa_circ_1418,RMVar_hsa_circ_87909,RMVar_hsa_circ_98461,RMVar_hsa_circ_306295,RMVar_hsa_circ_74266,RMVar_hsa_circ_245552,RMVar_hsa_circ_245553,RMVar_hsa_circ_99589,RMVar_hsa_circ_319221,RMVar_hsa_circ_74779,RMVar_hsa_circ_245554,RMVar_hsa_circ_245555,RMVar_hsa_circ_325430,RMVar_hsa_circ_318930,RMVar_hsa_circ_15416,RMVar_hsa_circ_372776,RMVar_hsa_circ_49126,RMVar_hsa_circ_245558,RMVar_hsa_circ_293924,RMVar_hsa_circ_371252,RMVar_hsa_circ_378325,RMVar_hsa_circ_307773,RMVar_hsa_circ_292795,RMVar_hsa_circ_70156,RMVar_hsa_circ_273435,RMVar_hsa_circ_69359,RMVar_hsa_circ_245561,RMVar_hsa_circ_245563,RMVar_hsa_circ_245564,RMVar_hsa_circ_245562,RMVar_hsa_circ_245560 30654 RMVar_ID_30654 Human_SNP_ID_326017455 A-to-I Human chr7 - 73461815 73461815 73461815 AAAATGCTAGGATTATAGGCATGAGCCACCTCACCCAGCCAACATATGTGCTCTTATAGTTTTGT AAAATGCTAGGATTATAGGCATGAGCCACCTCGCCCAGCCAACATATGTGCTCTTATAGTTTTGT T C BAZ1B Ensembl:ENSG00000009954 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1423473184 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59672,RMVar_hsa_circ_1418,RMVar_hsa_circ_87909,RMVar_hsa_circ_98461,RMVar_hsa_circ_306295,RMVar_hsa_circ_74266,RMVar_hsa_circ_245552,RMVar_hsa_circ_245553,RMVar_hsa_circ_99589,RMVar_hsa_circ_319221,RMVar_hsa_circ_74779,RMVar_hsa_circ_245554,RMVar_hsa_circ_245555,RMVar_hsa_circ_325430,RMVar_hsa_circ_318930,RMVar_hsa_circ_15416,RMVar_hsa_circ_372776,RMVar_hsa_circ_49126,RMVar_hsa_circ_245558,RMVar_hsa_circ_293924,RMVar_hsa_circ_371252,RMVar_hsa_circ_378325,RMVar_hsa_circ_307773,RMVar_hsa_circ_292795,RMVar_hsa_circ_70156,RMVar_hsa_circ_273435,RMVar_hsa_circ_69359,RMVar_hsa_circ_245561,RMVar_hsa_circ_245563,RMVar_hsa_circ_245564,RMVar_hsa_circ_245562,RMVar_hsa_circ_245560 30655 RMVar_ID_30655 Human_SNP_ID_326017459 A-to-I Human chr7 - 73461827 73461827 73461827 CCTCAGCCTCTCAAAATGCTAGGATTATAGGCATGAGCCACCTCACCCAGCCAACATATGTGCTC CCTCAGCCTCTCAAAATGCTAGGATTATAGGCGTGAGCCACCTCACCCAGCCAACATATGTGCTC T C BAZ1B Ensembl:ENSG00000009954 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1554570423 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59672,RMVar_hsa_circ_1418,RMVar_hsa_circ_87909,RMVar_hsa_circ_98461,RMVar_hsa_circ_306295,RMVar_hsa_circ_74266,RMVar_hsa_circ_245552,RMVar_hsa_circ_245553,RMVar_hsa_circ_99589,RMVar_hsa_circ_319221,RMVar_hsa_circ_74779,RMVar_hsa_circ_245554,RMVar_hsa_circ_245555,RMVar_hsa_circ_325430,RMVar_hsa_circ_318930,RMVar_hsa_circ_15416,RMVar_hsa_circ_372776,RMVar_hsa_circ_49126,RMVar_hsa_circ_245558,RMVar_hsa_circ_293924,RMVar_hsa_circ_371252,RMVar_hsa_circ_378325,RMVar_hsa_circ_307773,RMVar_hsa_circ_292795,RMVar_hsa_circ_70156,RMVar_hsa_circ_273435,RMVar_hsa_circ_69359,RMVar_hsa_circ_245561,RMVar_hsa_circ_245563,RMVar_hsa_circ_245564,RMVar_hsa_circ_245562,RMVar_hsa_circ_245560 30656 RMVar_ID_30656 Human_SNP_ID_326017467 A-to-I Human chr7 - 73461860 73461860 73461860 ATCTCAAACTCCAGGCTTCATGAGATCCTCCTACCTCAGCCTCTCAAAATGCTAGGATTATAGGC ATCTCAAACTCCAGGCTTCATGAGATCCTCCTGCCTCAGCCTCTCAAAATGCTAGGATTATAGGC T C BAZ1B Ensembl:ENSG00000009954 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1211904682 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59672,RMVar_hsa_circ_1418,RMVar_hsa_circ_87909,RMVar_hsa_circ_98461,RMVar_hsa_circ_306295,RMVar_hsa_circ_74266,RMVar_hsa_circ_245552,RMVar_hsa_circ_245553,RMVar_hsa_circ_99589,RMVar_hsa_circ_319221,RMVar_hsa_circ_74779,RMVar_hsa_circ_245554,RMVar_hsa_circ_245555,RMVar_hsa_circ_325430,RMVar_hsa_circ_318930,RMVar_hsa_circ_15416,RMVar_hsa_circ_372776,RMVar_hsa_circ_49126,RMVar_hsa_circ_245558,RMVar_hsa_circ_293924,RMVar_hsa_circ_371252,RMVar_hsa_circ_378325,RMVar_hsa_circ_307773,RMVar_hsa_circ_292795,RMVar_hsa_circ_70156,RMVar_hsa_circ_273435,RMVar_hsa_circ_69359,RMVar_hsa_circ_245561,RMVar_hsa_circ_245563,RMVar_hsa_circ_245564,RMVar_hsa_circ_245562,RMVar_hsa_circ_245560 30657 RMVar_ID_30657 Human_SNP_ID_326017479 A-to-I Human chr7 - 73461907 73461907 73461907 CATGGAAAATTTTGTAGAGACAAAATCTCACTATGTTGCCCTGGCTGATCTCAAACTCCAGGCTT CATGGAAAATTTTGTAGAGACAAAATCTCACTGTGTTGCCCTGGCTGATCTCAAACTCCAGGCTT T C BAZ1B Ensembl:ENSG00000009954 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs976449575 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59672,RMVar_hsa_circ_1418,RMVar_hsa_circ_87909,RMVar_hsa_circ_98461,RMVar_hsa_circ_306295,RMVar_hsa_circ_74266,RMVar_hsa_circ_245552,RMVar_hsa_circ_245553,RMVar_hsa_circ_99589,RMVar_hsa_circ_319221,RMVar_hsa_circ_74779,RMVar_hsa_circ_245554,RMVar_hsa_circ_245555,RMVar_hsa_circ_325430,RMVar_hsa_circ_318930,RMVar_hsa_circ_15416,RMVar_hsa_circ_372776,RMVar_hsa_circ_49126,RMVar_hsa_circ_245558,RMVar_hsa_circ_293924,RMVar_hsa_circ_371252,RMVar_hsa_circ_378325,RMVar_hsa_circ_307773,RMVar_hsa_circ_292795,RMVar_hsa_circ_70156,RMVar_hsa_circ_273435,RMVar_hsa_circ_69359,RMVar_hsa_circ_245561,RMVar_hsa_circ_245563,RMVar_hsa_circ_245564,RMVar_hsa_circ_245562,RMVar_hsa_circ_245560 30658 RMVar_ID_30658 Human_SNP_ID_326017481 A-to-I Human chr7 - 73461910 73461910 73461910 ACACATGGAAAATTTTGTAGAGACAAAATCTCACTATGTTGCCCTGGCTGATCTCAAACTCCAGG ACACATGGAAAATTTTGTAGAGACAAAATCTCTCTATGTTGCCCTGGCTGATCTCAAACTCCAGG T A BAZ1B Ensembl:ENSG00000009954 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1466474577 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59672,RMVar_hsa_circ_1418,RMVar_hsa_circ_87909,RMVar_hsa_circ_98461,RMVar_hsa_circ_306295,RMVar_hsa_circ_74266,RMVar_hsa_circ_245552,RMVar_hsa_circ_245553,RMVar_hsa_circ_99589,RMVar_hsa_circ_319221,RMVar_hsa_circ_74779,RMVar_hsa_circ_245554,RMVar_hsa_circ_245555,RMVar_hsa_circ_325430,RMVar_hsa_circ_318930,RMVar_hsa_circ_15416,RMVar_hsa_circ_372776,RMVar_hsa_circ_49126,RMVar_hsa_circ_245558,RMVar_hsa_circ_293924,RMVar_hsa_circ_371252,RMVar_hsa_circ_378325,RMVar_hsa_circ_307773,RMVar_hsa_circ_292795,RMVar_hsa_circ_70156,RMVar_hsa_circ_273435,RMVar_hsa_circ_69359,RMVar_hsa_circ_245561,RMVar_hsa_circ_245563,RMVar_hsa_circ_245564,RMVar_hsa_circ_245562,RMVar_hsa_circ_245560 30659 RMVar_ID_30659 Human_SNP_ID_326017482 A-to-I Human chr7 - 73461910 73461910 73461910 ACACATGGAAAATTTTGTAGAGACAAAATCTCACTATGTTGCCCTGGCTGATCTCAAACTCCAGG ACACATGGAAAATTTTGTAGAGACAAAATCTCGCTATGTTGCCCTGGCTGATCTCAAACTCCAGG T C BAZ1B Ensembl:ENSG00000009954 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1466474577 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59672,RMVar_hsa_circ_1418,RMVar_hsa_circ_87909,RMVar_hsa_circ_98461,RMVar_hsa_circ_306295,RMVar_hsa_circ_74266,RMVar_hsa_circ_245552,RMVar_hsa_circ_245553,RMVar_hsa_circ_99589,RMVar_hsa_circ_319221,RMVar_hsa_circ_74779,RMVar_hsa_circ_245554,RMVar_hsa_circ_245555,RMVar_hsa_circ_325430,RMVar_hsa_circ_318930,RMVar_hsa_circ_15416,RMVar_hsa_circ_372776,RMVar_hsa_circ_49126,RMVar_hsa_circ_245558,RMVar_hsa_circ_293924,RMVar_hsa_circ_371252,RMVar_hsa_circ_378325,RMVar_hsa_circ_307773,RMVar_hsa_circ_292795,RMVar_hsa_circ_70156,RMVar_hsa_circ_273435,RMVar_hsa_circ_69359,RMVar_hsa_circ_245561,RMVar_hsa_circ_245563,RMVar_hsa_circ_245564,RMVar_hsa_circ_245562,RMVar_hsa_circ_245560 30660 RMVar_ID_30660 Human_SNP_ID_326017509 A-to-I Human chr7 - 73462039 73462039 73462039 GTAGAGACGGGGCATGTTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCTAAGGCAGGAGGA GTAGAGACGGGGCATGTTGGCTCACGCCTATAGTCCCAGCACTTTGGGAGGCTAAGGCAGGAGGA T C BAZ1B Ensembl:ENSG00000009954 Protein coding intron GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs1414465979 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59672,RMVar_hsa_circ_1418,RMVar_hsa_circ_87909,RMVar_hsa_circ_98461,RMVar_hsa_circ_306295,RMVar_hsa_circ_74266,RMVar_hsa_circ_245552,RMVar_hsa_circ_245553,RMVar_hsa_circ_99589,RMVar_hsa_circ_319221,RMVar_hsa_circ_74779,RMVar_hsa_circ_245554,RMVar_hsa_circ_245555,RMVar_hsa_circ_325430,RMVar_hsa_circ_318930,RMVar_hsa_circ_15416,RMVar_hsa_circ_372776,RMVar_hsa_circ_49126,RMVar_hsa_circ_245558,RMVar_hsa_circ_293924,RMVar_hsa_circ_371252,RMVar_hsa_circ_378325,RMVar_hsa_circ_307773,RMVar_hsa_circ_292795,RMVar_hsa_circ_70156,RMVar_hsa_circ_273435,RMVar_hsa_circ_69359,RMVar_hsa_circ_245561,RMVar_hsa_circ_245563,RMVar_hsa_circ_245564,RMVar_hsa_circ_245562,RMVar_hsa_circ_245560 30661 RMVar_ID_30661 Human_SNP_ID_326017511 A-to-I Human chr7 - 73462042 73462042 73462042 TTTGTAGAGACGGGGCATGTTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCTAAGGCAGGA TTTGTAGAGACGGGGCATGTTGGCTCACGCCTTTAATCCCAGCACTTTGGGAGGCTAAGGCAGGA T A BAZ1B Ensembl:ENSG00000009954 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1174335829 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_842533 RMVar_hsa_circ_59672,RMVar_hsa_circ_1418,RMVar_hsa_circ_87909,RMVar_hsa_circ_98461,RMVar_hsa_circ_306295,RMVar_hsa_circ_74266,RMVar_hsa_circ_245552,RMVar_hsa_circ_245553,RMVar_hsa_circ_99589,RMVar_hsa_circ_319221,RMVar_hsa_circ_74779,RMVar_hsa_circ_245554,RMVar_hsa_circ_245555,RMVar_hsa_circ_325430,RMVar_hsa_circ_318930,RMVar_hsa_circ_15416,RMVar_hsa_circ_372776,RMVar_hsa_circ_49126,RMVar_hsa_circ_245558,RMVar_hsa_circ_293924,RMVar_hsa_circ_371252,RMVar_hsa_circ_378325,RMVar_hsa_circ_307773,RMVar_hsa_circ_292795,RMVar_hsa_circ_70156,RMVar_hsa_circ_273435,RMVar_hsa_circ_69359,RMVar_hsa_circ_245561,RMVar_hsa_circ_245563,RMVar_hsa_circ_245564,RMVar_hsa_circ_245562,RMVar_hsa_circ_245560 30662 RMVar_ID_30662 Human_SNP_ID_326017512 A-to-I Human chr7 - 73462042 73462042 73462042 TTTGTAGAGACGGGGCATGTTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCTAAGGCAGGA TTTGTAGAGACGGGGCATGTTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTAAGGCAGGA T C BAZ1B Ensembl:ENSG00000009954 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1174335829 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_842533 RMVar_hsa_circ_59672,RMVar_hsa_circ_1418,RMVar_hsa_circ_87909,RMVar_hsa_circ_98461,RMVar_hsa_circ_306295,RMVar_hsa_circ_74266,RMVar_hsa_circ_245552,RMVar_hsa_circ_245553,RMVar_hsa_circ_99589,RMVar_hsa_circ_319221,RMVar_hsa_circ_74779,RMVar_hsa_circ_245554,RMVar_hsa_circ_245555,RMVar_hsa_circ_325430,RMVar_hsa_circ_318930,RMVar_hsa_circ_15416,RMVar_hsa_circ_372776,RMVar_hsa_circ_49126,RMVar_hsa_circ_245558,RMVar_hsa_circ_293924,RMVar_hsa_circ_371252,RMVar_hsa_circ_378325,RMVar_hsa_circ_307773,RMVar_hsa_circ_292795,RMVar_hsa_circ_70156,RMVar_hsa_circ_273435,RMVar_hsa_circ_69359,RMVar_hsa_circ_245561,RMVar_hsa_circ_245563,RMVar_hsa_circ_245564,RMVar_hsa_circ_245562,RMVar_hsa_circ_245560 30663 RMVar_ID_30663 Human_SNP_ID_326018959 A-to-I Human chr7 - 73467646 73467646 73467646 CCAACTGAGGCTGGATGCAGTGGCTGATGCCTATAATCCCAGCACTTTGGGAGGCTGAGGCAGGC CCAACTGAGGCTGGATGCAGTGGCTGATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGC T C BAZ1B Ensembl:ENSG00000009954 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs782179659 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26115683 RMVar_hsa_circ_59672,RMVar_hsa_circ_87909,RMVar_hsa_circ_306295,RMVar_hsa_circ_245553,RMVar_hsa_circ_99589,RMVar_hsa_circ_319221,RMVar_hsa_circ_245554,RMVar_hsa_circ_245555,RMVar_hsa_circ_15416,RMVar_hsa_circ_371252,RMVar_hsa_circ_378325,RMVar_hsa_circ_292795,RMVar_hsa_circ_70156,RMVar_hsa_circ_273435,RMVar_hsa_circ_69359,RMVar_hsa_circ_51151,RMVar_hsa_circ_245563,RMVar_hsa_circ_245564,RMVar_hsa_circ_245562,RMVar_hsa_circ_245566,RMVar_hsa_circ_36970,RMVar_hsa_circ_273745,RMVar_hsa_circ_13774,RMVar_hsa_circ_127994,RMVar_hsa_circ_359696,RMVar_hsa_circ_297727,RMVar_hsa_circ_267533,RMVar_hsa_circ_113364,RMVar_hsa_circ_245567,RMVar_hsa_circ_245569,RMVar_hsa_circ_245570,RMVar_hsa_circ_245568,RMVar_hsa_circ_245572,RMVar_hsa_circ_116808 30664 RMVar_ID_30664 Human_SNP_ID_326020188 A-to-I Human chr7 - 73472440 73472440 73472440 CAGCCTGACCAACATGAAGAAACCTTGTCTCTACTAAAAATACAAAATTAGCCGGGCGTGGTGAC CAGCCTGACCAACATGAAGAAACCTTGTCTCTTCTAAAAATACAAAATTAGCCGGGCGTGGTGAC T A BAZ1B Ensembl:ENSG00000009954 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs770042812 Functional Loss SNV dbSNP153 33..33 33 - - - 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 30665 RMVar_ID_30665 Human_SNP_ID_326020477 A-to-I Human chr7 - 73473370 73473370 73473370 TTTTGTATTTTTAGTAGAGATGGGGATTCACCATGTTGGTTAGGCTGGTCCCAAAACTCTGACCT TTTTGTATTTTTAGTAGAGATGGGGATTCACCGTGTTGGTTAGGCTGGTCCCAAAACTCTGACCT T C BAZ1B Ensembl:ENSG00000009954 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1554572311 Functional Loss SNV dbSNP153 33..33 33 - - - 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 30666 RMVar_ID_30666 Human_SNP_ID_326020484 A-to-I Human chr7 - 73473390 73473390 73473390 TGCTACCACACTCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGATTCACCATGTTGGTTAGGC TGCTACCACACTCAGCTAATTTTTGTATTTTTGGTAGAGATGGGGATTCACCATGTTGGTTAGGC T C BAZ1B Ensembl:ENSG00000009954 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1268472195 Functional Loss SNV dbSNP153 33..33 33 - - - 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 30667 RMVar_ID_30667 Human_SNP_ID_326020488 A-to-I Human chr7 - 73473405 73473405 73473405 GGATAACAAGGCATCTGCTACCACACTCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGATTCA GGATAACAAGGCATCTGCTACCACACTCAGCTGATTTTTGTATTTTTAGTAGAGATGGGGATTCA T C BAZ1B Ensembl:ENSG00000009954 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1289054543 Functional Loss SNV dbSNP153 33..33 33 - - - 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 30668 RMVar_ID_30668 Human_SNP_ID_326020510 A-to-I Human chr7 - 73473467 73473467 73473467 TCACTGCAACCTCCACCTCCCAGGTTCAAGCTATTCTCGTGCCTCAGCCTCCTGAGTAGCTGGGA TCACTGCAACCTCCACCTCCCAGGTTCAAGCTGTTCTCGTGCCTCAGCCTCCTGAGTAGCTGGGA T C BAZ1B Ensembl:ENSG00000009954 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1016407684 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2491316,Human_miRNA_ID_2713685,Human_miRNA_ID_3049663 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 30669 RMVar_ID_30669 Human_SNP_ID_326020512 A-to-I Human chr7 - 73473471 73473471 73473471 TGGCTCACTGCAACCTCCACCTCCCAGGTTCAAGCTATTCTCGTGCCTCAGCCTCCTGAGTAGCT TGGCTCACTGCAACCTCCACCTCCCAGGTTCAGGCTATTCTCGTGCCTCAGCCTCCTGAGTAGCT T C BAZ1B Ensembl:ENSG00000009954 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1554572336 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2491316,Human_miRNA_ID_3049663 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 30670 RMVar_ID_30670 Human_SNP_ID_326020594 A-to-I Human chr7 - 73473767 73473767 73473767 TGGAGGCTGGTATTGAACCCCTAAACTCAAGCAATCTTCCTGCTTCAGCCTCCTAAAGTGCTGGG TGGAGGCTGGTATTGAACCCCTAAACTCAAGCCATCTTCCTGCTTCAGCCTCCTAAAGTGCTGGG T G BAZ1B Ensembl:ENSG00000009954 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1554572393 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17577784 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 30671 RMVar_ID_30671 Human_SNP_ID_326021106 A-to-I Human chr7 - 73475812 73475812 73475812 TCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCATGCGCCATCATGCCTG TCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTTGCTGGGATTACAGGCATGCGCCATCATGCCTG T A BAZ1B Ensembl:ENSG00000009954 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1047969125 Functional Loss SNV dbSNP153 33..33 33 - - - 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 30672 RMVar_ID_30672 Human_SNP_ID_326022519 A-to-I Human chr7 - 73481271 73481271 73481271 CGCCTGCCTCGGCCTCCCAGAGTGCTGGGATTACAGGCGTGAACCACCACGCCCAGCCCCTAATG CGCCTGCCTCGGCCTCCCAGAGTGCTGGGATTGCAGGCGTGAACCACCACGCCCAGCCCCTAATG T C BAZ1B Ensembl:ENSG00000009954 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1030760230 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59672,RMVar_hsa_circ_87909,RMVar_hsa_circ_245553,RMVar_hsa_circ_99589,RMVar_hsa_circ_245554,RMVar_hsa_circ_378325,RMVar_hsa_circ_70156,RMVar_hsa_circ_69359,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_43788,RMVar_hsa_circ_103602,RMVar_hsa_circ_245574,RMVar_hsa_circ_245575,RMVar_hsa_circ_355948,RMVar_hsa_circ_358503,RMVar_hsa_circ_324136,RMVar_hsa_circ_245577,RMVar_hsa_circ_351191,RMVar_hsa_circ_359490 30673 RMVar_ID_30673 Human_SNP_ID_326023191 A-to-I Human chr7 - 73483806 73483806 73483806 GCGAGACCCTGTTTCTACATACACAAAAAATTAACTGGGTGTGGTGGCGTGTGCCTCTAGTCCAA GCGAGACCCTGTTTCTACATACACAAAAAATTGACTGGGTGTGGTGGCGTGTGCCTCTAGTCCAA T C BAZ1B Ensembl:ENSG00000009954 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs907377497 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59672,RMVar_hsa_circ_87909,RMVar_hsa_circ_245553,RMVar_hsa_circ_99589,RMVar_hsa_circ_245554,RMVar_hsa_circ_378325,RMVar_hsa_circ_70156,RMVar_hsa_circ_69359,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_43788,RMVar_hsa_circ_103602,RMVar_hsa_circ_245574,RMVar_hsa_circ_245575,RMVar_hsa_circ_355948,RMVar_hsa_circ_358503,RMVar_hsa_circ_324136,RMVar_hsa_circ_245577,RMVar_hsa_circ_351191,RMVar_hsa_circ_359490 30674 RMVar_ID_30674 Human_SNP_ID_326023268 A-to-I Human chr7 - 73484086 73484086 73484086 AATTTTTCTATTTTTGGTAGACATGGGGTTTCACCATGTTGGCCAGGATGGTCTCAATCCCTGGA AATTTTTCTATTTTTGGTAGACATGGGGTTTCGCCATGTTGGCCAGGATGGTCTCAATCCCTGGA T C BAZ1B Ensembl:ENSG00000009954 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1285046644 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59672,RMVar_hsa_circ_87909,RMVar_hsa_circ_245553,RMVar_hsa_circ_99589,RMVar_hsa_circ_245554,RMVar_hsa_circ_378325,RMVar_hsa_circ_70156,RMVar_hsa_circ_69359,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_43788,RMVar_hsa_circ_103602,RMVar_hsa_circ_245574,RMVar_hsa_circ_245575,RMVar_hsa_circ_355948,RMVar_hsa_circ_358503,RMVar_hsa_circ_324136,RMVar_hsa_circ_245577,RMVar_hsa_circ_351191,RMVar_hsa_circ_359490 30675 RMVar_ID_30675 Human_SNP_ID_326023286 A-to-I Human chr7 - 73484154 73484154 73484154 TCCAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCACCCACCACCATGCCTG TCCAGCGATTCTCCTGCCTCAGCCTCCCGAGTCGCTGGGACTACAGGCACCCACCACCATGCCTG T G BAZ1B Ensembl:ENSG00000009954 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1041133594 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59672,RMVar_hsa_circ_87909,RMVar_hsa_circ_245553,RMVar_hsa_circ_99589,RMVar_hsa_circ_245554,RMVar_hsa_circ_378325,RMVar_hsa_circ_70156,RMVar_hsa_circ_69359,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_43788,RMVar_hsa_circ_103602,RMVar_hsa_circ_245574,RMVar_hsa_circ_245575,RMVar_hsa_circ_355948,RMVar_hsa_circ_358503,RMVar_hsa_circ_324136,RMVar_hsa_circ_245577,RMVar_hsa_circ_351191,RMVar_hsa_circ_359490 30676 RMVar_ID_30676 Human_SNP_ID_326023576 A-to-I Human chr7 - 73485221 73485221 73485221 ATATGAATTTCTTAAAAACATTGATATTTGCTAGCTCACACCTGTGTAATTCTACACTTTGGGAG ATATGAATTTCTTAAAAACATTGATATTTGCTGGCTCACACCTGTGTAATTCTACACTTTGGGAG T C BAZ1B Ensembl:ENSG00000009954 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1554574318 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59672,RMVar_hsa_circ_87909,RMVar_hsa_circ_245553,RMVar_hsa_circ_99589,RMVar_hsa_circ_245554,RMVar_hsa_circ_378325,RMVar_hsa_circ_70156,RMVar_hsa_circ_69359,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_43788,RMVar_hsa_circ_103602,RMVar_hsa_circ_245574,RMVar_hsa_circ_245575,RMVar_hsa_circ_355948,RMVar_hsa_circ_358503,RMVar_hsa_circ_324136,RMVar_hsa_circ_245577,RMVar_hsa_circ_351191,RMVar_hsa_circ_359490 30677 RMVar_ID_30677 Human_SNP_ID_326025090 A-to-I Human chr7 - 73491120 73491120 73491120 CACCGTGCCCGGCTAAGTTTTGTATTTTTAGTAGATACGGGATTTCACTATGTTGGCCAGGCTGG CACCGTGCCCGGCTAAGTTTTGTATTTTTAGTCGATACGGGATTTCACTATGTTGGCCAGGCTGG T G BAZ1B Ensembl:ENSG00000009954 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1184279909 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87909,RMVar_hsa_circ_245553,RMVar_hsa_circ_99589,RMVar_hsa_circ_245554,RMVar_hsa_circ_378325,RMVar_hsa_circ_70156,RMVar_hsa_circ_69359,RMVar_hsa_circ_36970,RMVar_hsa_circ_127994,RMVar_hsa_circ_359696,RMVar_hsa_circ_245567,RMVar_hsa_circ_245568,RMVar_hsa_circ_43788,RMVar_hsa_circ_103602,RMVar_hsa_circ_245575,RMVar_hsa_circ_355948,RMVar_hsa_circ_324136,RMVar_hsa_circ_245577,RMVar_hsa_circ_359490,RMVar_hsa_circ_94846,RMVar_hsa_circ_321424,RMVar_hsa_circ_336686,RMVar_hsa_circ_305511,RMVar_hsa_circ_245581,RMVar_hsa_circ_245582,RMVar_hsa_circ_245580 30678 RMVar_ID_30678 Human_SNP_ID_326025120 A-to-I Human chr7 - 73491226 73491226 73491226 GCGGGAGTACAATGGCACGGTCTTGGCTCACTACAGCCTCTGCCTCTCGGATTCAAGCGATTCTC GCGGGAGTACAATGGCACGGTCTTGGCTCACTGCAGCCTCTGCCTCTCGGATTCAAGCGATTCTC T C BAZ1B Ensembl:ENSG00000009954 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1358660944 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2272199,Human_miRNA_ID_2713687,Human_miRNA_ID_3049665 RMVar_hsa_circ_87909,RMVar_hsa_circ_245553,RMVar_hsa_circ_99589,RMVar_hsa_circ_245554,RMVar_hsa_circ_378325,RMVar_hsa_circ_70156,RMVar_hsa_circ_69359,RMVar_hsa_circ_36970,RMVar_hsa_circ_127994,RMVar_hsa_circ_359696,RMVar_hsa_circ_245567,RMVar_hsa_circ_245568,RMVar_hsa_circ_43788,RMVar_hsa_circ_103602,RMVar_hsa_circ_245575,RMVar_hsa_circ_355948,RMVar_hsa_circ_324136,RMVar_hsa_circ_245577,RMVar_hsa_circ_359490,RMVar_hsa_circ_94846,RMVar_hsa_circ_321424,RMVar_hsa_circ_336686,RMVar_hsa_circ_305511,RMVar_hsa_circ_245581,RMVar_hsa_circ_245582,RMVar_hsa_circ_245580 30679 RMVar_ID_30679 Human_SNP_ID_326027501 A-to-I Human chr7 - 73499580 73499580 73499580 TTCCTGCCTCAGCCTCCTCCGTAGTTAAGACTATGGGAACACGCCATCATGCTTGGCTAATTTTA TTCCTGCCTCAGCCTCCTCCGTAGTTAAGACTGTGGGAACACGCCATCATGCTTGGCTAATTTTA T C BAZ1B Ensembl:ENSG00000009954 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs533987259 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99589,RMVar_hsa_circ_245554,RMVar_hsa_circ_70156,RMVar_hsa_circ_127994,RMVar_hsa_circ_245567,RMVar_hsa_circ_103602,RMVar_hsa_circ_245575,RMVar_hsa_circ_324136,RMVar_hsa_circ_245577,RMVar_hsa_circ_94846,RMVar_hsa_circ_321424,RMVar_hsa_circ_336686,RMVar_hsa_circ_245581,RMVar_hsa_circ_245580,RMVar_hsa_circ_356242,RMVar_hsa_circ_346243,RMVar_hsa_circ_245583,RMVar_hsa_circ_338837,RMVar_hsa_circ_367448 30680 RMVar_ID_30680 Human_SNP_ID_326027615 A-to-I Human chr7 - 73500059 73500059 73500059 CTGTAGTCCCAGCTACTTAGGAGGCTGAGGCGAGAGAATTGCTTGAGCCCAGAAGTTCAAGGCCA CTGTAGTCCCAGCTACTTAGGAGGCTGAGGCGGGAGAATTGCTTGAGCCCAGAAGTTCAAGGCCA T C BAZ1B Ensembl:ENSG00000009954 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs556218335 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99589,RMVar_hsa_circ_245554,RMVar_hsa_circ_70156,RMVar_hsa_circ_127994,RMVar_hsa_circ_245567,RMVar_hsa_circ_103602,RMVar_hsa_circ_245575,RMVar_hsa_circ_324136,RMVar_hsa_circ_245577,RMVar_hsa_circ_94846,RMVar_hsa_circ_321424,RMVar_hsa_circ_336686,RMVar_hsa_circ_245581,RMVar_hsa_circ_245580,RMVar_hsa_circ_356242,RMVar_hsa_circ_346243,RMVar_hsa_circ_245583,RMVar_hsa_circ_338837,RMVar_hsa_circ_367448 30681 RMVar_ID_30681 Human_SNP_ID_326027616 A-to-I Human chr7 - 73500059 73500059 73500059 CTGTAGTCCCAGCTACTTAGGAGGCTGAGGCGAGAGAATTGCTTGAGCCCAGAAGTTCAAGGCCA CTGTAGTCCCAGCTACTTAGGAGGCTGAGGCGCGAGAATTGCTTGAGCCCAGAAGTTCAAGGCCA T G BAZ1B Ensembl:ENSG00000009954 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs556218335 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99589,RMVar_hsa_circ_245554,RMVar_hsa_circ_70156,RMVar_hsa_circ_127994,RMVar_hsa_circ_245567,RMVar_hsa_circ_103602,RMVar_hsa_circ_245575,RMVar_hsa_circ_324136,RMVar_hsa_circ_245577,RMVar_hsa_circ_94846,RMVar_hsa_circ_321424,RMVar_hsa_circ_336686,RMVar_hsa_circ_245581,RMVar_hsa_circ_245580,RMVar_hsa_circ_356242,RMVar_hsa_circ_346243,RMVar_hsa_circ_245583,RMVar_hsa_circ_338837,RMVar_hsa_circ_367448 30682 RMVar_ID_30682 Human_SNP_ID_326028576 A-to-I Human chr7 - 73503574 73503574 73503574 AGCTAGGAGTTTGAGACCAGCCTGGGCAACATAGGGAGACCCTGTTTCTACAAAAAATAATAAAA AGCTAGGAGTTTGAGACCAGCCTGGGCAACATCGGGAGACCCTGTTTCTACAAAAAATAATAAAA T G BAZ1B Ensembl:ENSG00000009954 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1337020972 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99589,RMVar_hsa_circ_245554,RMVar_hsa_circ_70156,RMVar_hsa_circ_127994,RMVar_hsa_circ_245567,RMVar_hsa_circ_103602,RMVar_hsa_circ_245575,RMVar_hsa_circ_324136,RMVar_hsa_circ_245577,RMVar_hsa_circ_94846,RMVar_hsa_circ_321424,RMVar_hsa_circ_336686,RMVar_hsa_circ_245581,RMVar_hsa_circ_245580,RMVar_hsa_circ_356242,RMVar_hsa_circ_346243,RMVar_hsa_circ_245583,RMVar_hsa_circ_338837,RMVar_hsa_circ_367448 30683 RMVar_ID_30683 Human_SNP_ID_326029097 A-to-I Human chr7 - 73505739 73505739 73505739 TGAGACCAGCCTGGCCAACATGGCGATACCCTATCTCTCCAAAAAATACAAAAATTAGCCAGGTA TGAGACCAGCCTGGCCAACATGGCGATACCCTTTCTCTCCAAAAAATACAAAAATTAGCCAGGTA T A BAZ1B Ensembl:ENSG00000009954 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1012874164 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99589,RMVar_hsa_circ_245554,RMVar_hsa_circ_70156,RMVar_hsa_circ_127994,RMVar_hsa_circ_245567,RMVar_hsa_circ_103602,RMVar_hsa_circ_245575,RMVar_hsa_circ_324136,RMVar_hsa_circ_245577,RMVar_hsa_circ_94846,RMVar_hsa_circ_321424,RMVar_hsa_circ_336686,RMVar_hsa_circ_245581,RMVar_hsa_circ_245580,RMVar_hsa_circ_356242,RMVar_hsa_circ_346243,RMVar_hsa_circ_245583,RMVar_hsa_circ_338837,RMVar_hsa_circ_367448 30684 RMVar_ID_30684 Human_SNP_ID_326029098 A-to-I Human chr7 - 73505739 73505739 73505739 TGAGACCAGCCTGGCCAACATGGCGATACCCTATCTCTCCAAAAAATACAAAAATTAGCCAGGTA TGAGACCAGCCTGGCCAACATGGCGATACCCTGTCTCTCCAAAAAATACAAAAATTAGCCAGGTA T C BAZ1B Ensembl:ENSG00000009954 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1012874164 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99589,RMVar_hsa_circ_245554,RMVar_hsa_circ_70156,RMVar_hsa_circ_127994,RMVar_hsa_circ_245567,RMVar_hsa_circ_103602,RMVar_hsa_circ_245575,RMVar_hsa_circ_324136,RMVar_hsa_circ_245577,RMVar_hsa_circ_94846,RMVar_hsa_circ_321424,RMVar_hsa_circ_336686,RMVar_hsa_circ_245581,RMVar_hsa_circ_245580,RMVar_hsa_circ_356242,RMVar_hsa_circ_346243,RMVar_hsa_circ_245583,RMVar_hsa_circ_338837,RMVar_hsa_circ_367448 30685 RMVar_ID_30685 Human_SNP_ID_326029099 A-to-I Human chr7 - 73505739 73505739 73505739 TGAGACCAGCCTGGCCAACATGGCGATACCCTATCTCTCCAAAAAATACAAAAATTAGCCAGGTA TGAGACCAGCCTGGCCAACATGGCGATACCCTCTCTCTCCAAAAAATACAAAAATTAGCCAGGTA T G BAZ1B Ensembl:ENSG00000009954 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1012874164 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99589,RMVar_hsa_circ_245554,RMVar_hsa_circ_70156,RMVar_hsa_circ_127994,RMVar_hsa_circ_245567,RMVar_hsa_circ_103602,RMVar_hsa_circ_245575,RMVar_hsa_circ_324136,RMVar_hsa_circ_245577,RMVar_hsa_circ_94846,RMVar_hsa_circ_321424,RMVar_hsa_circ_336686,RMVar_hsa_circ_245581,RMVar_hsa_circ_245580,RMVar_hsa_circ_356242,RMVar_hsa_circ_346243,RMVar_hsa_circ_245583,RMVar_hsa_circ_338837,RMVar_hsa_circ_367448 30686 RMVar_ID_30686 Human_SNP_ID_326030005 A-to-I Human chr7 - 73508700 73508700 73508700 CCAAAAGTTAAGTCTTAAAAGAGGTTAGGTGCAGTGGTGCATGCCTGTGGTCCCAGCTACCTGAG CCAAAAGTTAAGTCTTAAAAGAGGTTAGGTGCGGTGGTGCATGCCTGTGGTCCCAGCTACCTGAG T C BAZ1B Ensembl:ENSG00000009954 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1353384599 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70156,RMVar_hsa_circ_127994,RMVar_hsa_circ_245567,RMVar_hsa_circ_103602,RMVar_hsa_circ_245575,RMVar_hsa_circ_94846,RMVar_hsa_circ_321424,RMVar_hsa_circ_245580,RMVar_hsa_circ_356242,RMVar_hsa_circ_367448,RMVar_hsa_circ_303102 30687 RMVar_ID_30687 Human_SNP_ID_326031381 A-to-I Human chr7 - 73513165 73513165 73513165 GAGGACTGTTTGAGCCCAGGAGTTCAAGACCAACCTGGGCAATGTGGTGAGACCCTGACTCTGCA GAGGACTGTTTGAGCCCAGGAGTTCAAGACCAGCCTGGGCAATGTGGTGAGACCCTGACTCTGCA T C BAZ1B Ensembl:ENSG00000009954 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1409696102 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94846,RMVar_hsa_circ_245580 30688 RMVar_ID_30688 Human_SNP_ID_326031854 A-to-I Human chr7 - 73514989 73514989 73514989 TGGCTCACTGCAACCTCCGCCTTCCTCATTCAAGCAGTTCTCTGCCTCAGCCTCCCGAGTAGCTG TGGCTCACTGCAACCTCCGCCTTCCTCATTCAGGCAGTTCTCTGCCTCAGCCTCCCGAGTAGCTG T C BAZ1B Ensembl:ENSG00000009954 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1457023556 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16212733 RMVar_hsa_circ_94846,RMVar_hsa_circ_245580 30689 RMVar_ID_30689 Human_SNP_ID_326032604 A-to-I Human chr7 - 73517282 73517282 73517282 TGCAAAGTTGCCCCGGCTGGTCTTGGATTTCTAGCCTCAAGTGATCCTCCCGCTTCAGCCTCCCA TGCAAAGTTGCCCCGGCTGGTCTTGGATTTCTGGCCTCAAGTGATCCTCCCGCTTCAGCCTCCCA T C BAZ1B Ensembl:ENSG00000009954 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1381954114 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16212853 RMVar_hsa_circ_94846,RMVar_hsa_circ_245580 30690 RMVar_ID_30690 Human_SNP_ID_326032643 A-to-I Human chr7 - 73517418 73517418 73517418 TGATCATGGCTTACTGCAGCCTCCAACTTCCCAGGCTCAAGTGATTCTTCCCACTCAGCCTGCTG TGATCATGGCTTACTGCAGCCTCCAACTTCCCCGGCTCAAGTGATTCTTCCCACTCAGCCTGCTG T G BAZ1B Ensembl:ENSG00000009954 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs782054986 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94846,RMVar_hsa_circ_245580 30691 RMVar_ID_30691 Human_SNP_ID_326032988 A-to-I Human chr7 - 73518606 73518606 73518606 CTTGAACCGGACTCAAGAGATCCTCCTGCCTCAGCCTCCAGAGTAGCTGGGACTACAGGCACGCA CTTGAACCGGACTCAAGAGATCCTCCTGCCTCGGCCTCCAGAGTAGCTGGGACTACAGGCACGCA T C BAZ1B Ensembl:ENSG00000009954 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1278467508 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16212918 RMVar_hsa_circ_94846,RMVar_hsa_circ_245580 30692 RMVar_ID_30692 Human_SNP_ID_326032992 A-to-I Human chr7 - 73518623 73518622 73518624 TGGTAGCACAGGGAAGCCTTGAACCGGACTCAAGAGATCCTCCTGCCTCAGCCTCCAGAGTAGCT TGGTAGCACAGGGAAGCCTTGAACCGGACTC__GAGATCCTCCTGCCTCAGCCTCCAGAGTAGCT CTT C BAZ1B Ensembl:ENSG00000009954 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1386508446 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_7756928,Human_RBP_ID_8670909,Human_RBP_ID_16212919 RMVar_hsa_circ_94846,RMVar_hsa_circ_245580 30693 RMVar_ID_30693 Human_SNP_ID_326038991 A-to-I Human chr7 - 73538779 73538779 73538779 AGATAGGGTCTTGCTCTGTTGCCCAGGCTAGAATGCAGTGGCTGAATCCTAGCTCACTGCAGTCT AGATAGGGTCTTGCTCTGTTGCCCAGGCTAGACTGCAGTGGCTGAATCCTAGCTCACTGCAGTCT T G BCL7B Ensembl:ENSG00000106635 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1563421770 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117969,RMVar_hsa_circ_245585 30694 RMVar_ID_30694 Human_SNP_ID_326040239 A-to-I Human chr7 - 73543314 73543314 73543314 AAGTTAGCTGAGCGTGGTGGCGCGTGCCTGTAATCCCAGCTACTCGGGGGTCTGAGACAGGAGAA AAGTTAGCTGAGCGTGGTGGCGCGTGCCTGTAGTCCCAGCTACTCGGGGGTCTGAGACAGGAGAA T C BCL7B Ensembl:ENSG00000106635 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1348133372 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_245586,RMVar_hsa_circ_290418 30695 RMVar_ID_30695 Human_SNP_ID_326040643 A-to-I Human chr7 - 73544964 73544964 73544964 GCCTCAAACTTTCAGGCTCAAGCGATCCTCCCACCTCAGCCTTCTCAGTAGCTGGGACCACCAGC GCCTCAAACTTTCAGGCTCAAGCGATCCTCCCCCCTCAGCCTTCTCAGTAGCTGGGACCACCAGC T G BCL7B Ensembl:ENSG00000106635 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1554583337 Functional Loss SNV dbSNP153 33..33 33 - - - 30696 RMVar_ID_30696 Human_SNP_ID_326043236 A-to-I Human chr7 - 73555214 73555214 73555214 TTTGTGGAGACCGGGTTTCACCATGTTGGCCAAGCTGGTCTTGAACTCCTGAATTCCAAGTGGTC TTTGTGGAGACCGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGAATTCCAAGTGGTC T C BCL7B Ensembl:ENSG00000106635 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1269111596 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3099491 30697 RMVar_ID_30697 Human_SNP_ID_326049499 A-to-I Human chr7 - 73577911 73577911 73577911 CACTGAGGCCAGGCGAAGTGGCTCACGCCTGTATTCCCAGCACTTTGGGAGGCCGAGGCAGGGAG CACTGAGGCCAGGCGAAGTGGCTCACGCCTGTGTTCCCAGCACTTTGGGAGGCCGAGGCAGGGAG T C TBL2 Ensembl:ENSG00000106638 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs894124589 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1942053,Human_miRNA_ID_1942054,Human_miRNA_ID_1945096,Human_miRNA_ID_1945097,Human_miRNA_ID_2085831,Human_miRNA_ID_2085832,Human_miRNA_ID_2116244,Human_miRNA_ID_2116245,Human_miRNA_ID_2199817,Human_miRNA_ID_2199818,Human_miRNA_ID_2202885,Human_miRNA_ID_2202886,Human_miRNA_ID_2315332,Human_miRNA_ID_2315333,Human_miRNA_ID_2318492,Human_miRNA_ID_2318493,Human_miRNA_ID_2321649,Human_miRNA_ID_2321650,Human_miRNA_ID_2324806,Human_miRNA_ID_2324807,Human_miRNA_ID_2327948,Human_miRNA_ID_2327949,Human_miRNA_ID_2519187,Human_miRNA_ID_2519188,Human_miRNA_ID_2522354,Human_miRNA_ID_2522355,Human_miRNA_ID_2774200,Human_miRNA_ID_2774201,Human_miRNA_ID_2815345,Human_miRNA_ID_2815346,Human_miRNA_ID_2821553,Human_miRNA_ID_2821554,Human_miRNA_ID_2827682,Human_miRNA_ID_2827683,Human_miRNA_ID_2830834,Human_miRNA_ID_2830835,Human_miRNA_ID_2834954,Human_miRNA_ID_2834955,Human_miRNA_ID_2840316,Human_miRNA_ID_2840317,Human_miRNA_ID_2845442,Human_miRNA_ID_2845443,Human_miRNA_ID_2848462,Human_miRNA_ID_2848463,Human_miRNA_ID_2862608,Human_miRNA_ID_2862609,Human_miRNA_ID_3112337,Human_miRNA_ID_3112338 30698 RMVar_ID_30698 Human_SNP_ID_326059016 A-to-I Human chr7 - 73609353 73609339 73609354 GTAATTCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGGGAGGTGGAGGTTGCA GTAATTCCAGCTACTTGGGAGGCTGAGGCAG_______________CCGGGAGGTGGAGGTTGCA GGTTCAAGCGATTCTC G MLXIPL,AC005089.1 Ensembl:ENSG00000009950,Ensembl:ENSG00000274080 Protein coding,lincRNA intron,exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1473697339 Functional Loss DEL dbSNP153 32..46 33 - - - RMVar_hsa_circ_119382,RMVar_hsa_circ_245588 30699 RMVar_ID_30699 Human_SNP_ID_326059019 A-to-I Human chr7 - 73609351 73609351 73609351 AATTCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGGGAGGTGGAGGTTGCAGT AATTCCAGCTACTTGGGAGGCTGAGGCAGGAGCATCGCTTGAACCCGGGAGGTGGAGGTTGCAGT T G MLXIPL,AC005089.1 Ensembl:ENSG00000009950,Ensembl:ENSG00000274080 Protein coding,lincRNA intron,exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1473195139 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119382,RMVar_hsa_circ_245588 30700 RMVar_ID_30700 Human_SNP_ID_326059150 A-to-I Human chr7 - 73609764 73609764 73609764 TGGAGGCTAAGGTAGGAGGATCACTTGCACCCAGGAGGCGGAGATCGAAGTACCCAAGATCCCTG TGGAGGCTAAGGTAGGAGGATCACTTGCACCCGGGAGGCGGAGATCGAAGTACCCAAGATCCCTG T C MLXIPL,AC005089.1 Ensembl:ENSG00000009950,Ensembl:ENSG00000274080 Protein coding,lincRNA intron,exon GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs764121317 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17577440 RMVar_hsa_circ_119382,RMVar_hsa_circ_245588 30701 RMVar_ID_30701 Human_SNP_ID_326059319 A-to-I Human chr7 - 73610625 73610625 73610625 ACCAAAAATACAAAAAACCAGCTGGGCATGGTAGCACATGCCTATAGTCCCAGCTACTCGGGAGG ACCAAAAATACAAAAAACCAGCTGGGCATGGTGGCACATGCCTATAGTCCCAGCTACTCGGGAGG T C MLXIPL,AC005089.1 Ensembl:ENSG00000009950,Ensembl:ENSG00000274080 Protein coding,lincRNA intron,exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1424194257 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5251251 RMVar_hsa_circ_119382,RMVar_hsa_circ_245588 30702 RMVar_ID_30702 Human_SNP_ID_326059322 A-to-I Human chr7 - 73610641 73610641 73610641 GCGAAACCCTGTCTCTACCAAAAATACAAAAAACCAGCTGGGCATGGTAGCACATGCCTATAGTC GCGAAACCCTGTCTCTACCAAAAATACAAAAACCCAGCTGGGCATGGTAGCACATGCCTATAGTC T G MLXIPL,AC005089.1 Ensembl:ENSG00000009950,Ensembl:ENSG00000274080 Protein coding,lincRNA intron,exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1478769013 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5251251 RMVar_hsa_circ_119382,RMVar_hsa_circ_245588 30703 RMVar_ID_30703 Human_SNP_ID_326059324 A-to-I Human chr7 - 73610645 73610645 73610645 CATGGCGAAACCCTGTCTCTACCAAAAATACAAAAAACCAGCTGGGCATGGTAGCACATGCCTAT CATGGCGAAACCCTGTCTCTACCAAAAATACAGAAAACCAGCTGGGCATGGTAGCACATGCCTAT T C MLXIPL,AC005089.1 Ensembl:ENSG00000009950,Ensembl:ENSG00000274080 Protein coding,lincRNA intron,exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1203754595 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5251251 RMVar_hsa_circ_119382,RMVar_hsa_circ_245588 30704 RMVar_ID_30704 Human_SNP_ID_326059414 A-to-I Human chr7 - 73610997 73610997 73610997 CAACATGGAGAAACCCTGTCTCTACTAAAAATACAAAAATTAGTGGGGCGTGGTGGCGCTCACCT CAACATGGAGAAACCCTGTCTCTACTAAAAATGCAAAAATTAGTGGGGCGTGGTGGCGCTCACCT T C MLXIPL,AC005089.1 Ensembl:ENSG00000009950,Ensembl:ENSG00000274080 Protein coding,lincRNA intron,exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1034713038 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119382,RMVar_hsa_circ_245588 30705 RMVar_ID_30705 Human_SNP_ID_326059653 A-to-I Human chr7 - 73612080 73612080 73612080 CTCAAGCAATCCTCTCAGTTCAGCCTCCCAAAATGTTGGGGCTACAGGCGTGAGCCACCACACCG CTCAAGCAATCCTCTCAGTTCAGCCTCCCAAAGTGTTGGGGCTACAGGCGTGAGCCACCACACCG T C MLXIPL Ensembl:ENSG00000009950 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1554599850 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22325422 RMVar_hsa_circ_119382,RMVar_hsa_circ_245588 30706 RMVar_ID_30706 Human_SNP_ID_326060440 A-to-I Human chr7 - 73615089 73615089 73615089 TTATCTATAAAAACGAGGCCACGGTGGCTCACACCTGTAATCCCAGCACTTTGGAAGGCCAAGGC TTATCTATAAAAACGAGGCCACGGTGGCTCACTCCTGTAATCCCAGCACTTTGGAAGGCCAAGGC T A MLXIPL Ensembl:ENSG00000009950 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs887881881 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22731187 RMVar_hsa_circ_119382,RMVar_hsa_circ_245588 30707 RMVar_ID_30707 Human_SNP_ID_326060441 A-to-I Human chr7 - 73615089 73615089 73615089 TTATCTATAAAAACGAGGCCACGGTGGCTCACACCTGTAATCCCAGCACTTTGGAAGGCCAAGGC TTATCTATAAAAACGAGGCCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGAAGGCCAAGGC T C MLXIPL Ensembl:ENSG00000009950 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs887881881 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22731187 RMVar_hsa_circ_119382,RMVar_hsa_circ_245588 30708 RMVar_ID_30708 Human_SNP_ID_326078054 A-to-I Human chr7 - 73680651 73680651 73680651 AAGTGCCTGTAGTCCCAGCTACTCAGGAGGCTAAGGTGGGAGAATCGCTTGAGCCTGAGAGGTCG AAGTGCCTGTAGTCCCAGCTACTCAGGAGGCTCAGGTGGGAGAATCGCTTGAGCCTGAGAGGTCG T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1336575908 Functional Loss SNV dbSNP153 33..33 33 - - - 30709 RMVar_ID_30709 Human_SNP_ID_326099150 A-to-I Human chr7 + 73756259 73756259 73756259 CGAGTCTCACTTTGTCACCCAGGCAGTGCAGTAGTGCAATCTCGGCTCACTGCAACCTCCGCCTC CGAGTCTCACTTTGTCACCCAGGCAGTGCAGTGGTGCAATCTCGGCTCACTGCAACCTCCGCCTC A G RF00017-4508 RNACentral:URS000093D619 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1554625296 Functional Loss SNV dbSNP153 33..33 33 - - - 30710 RMVar_ID_30710 Human_SNP_ID_326118811 A-to-I Human chr7 - 73832964 73832964 73832964 TAATTTTTTTAACTTTTTGTAGAGATGGTGCCACTATGTTCCCCAGGCTGGTCTCAAACTCCTGC TAATTTTTTTAACTTTTTGTAGAGATGGTGCCGCTATGTTCCCCAGGCTGGTCTCAAACTCCTGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1187095357 Functional Loss SNV dbSNP153 33..33 33 - - - 30711 RMVar_ID_30711 Human_SNP_ID_326118812 A-to-I Human chr7 - 73832964 73832964 73832964 TAATTTTTTTAACTTTTTGTAGAGATGGTGCCACTATGTTCCCCAGGCTGGTCTCAAACTCCTGC TAATTTTTTTAACTTTTTGTAGAGATGGTGCCCCTATGTTCCCCAGGCTGGTCTCAAACTCCTGC T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1187095357 Functional Loss SNV dbSNP153 33..33 33 - - - 30712 RMVar_ID_30712 Human_SNP_ID_326119171 A-to-I Human chr7 - 73834297 73834297 73834297 TACTAAAAATACAAAAATTAGCTGGGCATGGTAGCACACCCCTGTAATCCCAGCTAGTTGCGAGG TACTAAAAATACAAAAATTAGCTGGGCATGGTGGCACACCCCTGTAATCCCAGCTAGTTGCGAGG T C lnc-CLDN3-1 RNACentral:URS00009BA700 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1393298901 Functional Loss SNV dbSNP153 33..33 33 - - - 30713 RMVar_ID_30713 Human_SNP_ID_326119178 A-to-I Human chr7 - 73834310 73834310 73834310 GAAACCCTGTCTCTACTAAAAATACAAAAATTAGCTGGGCATGGTAGCACACCCCTGTAATCCCA GAAACCCTGTCTCTACTAAAAATACAAAAATTGGCTGGGCATGGTAGCACACCCCTGTAATCCCA T C lnc-CLDN3-1 RNACentral:URS00009BA700 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs553864840 Functional Loss SNV dbSNP153 33..33 33 - - - 30714 RMVar_ID_30714 Human_SNP_ID_326164992 A-to-I Human chr7 - 74011478 74011478 74011478 CTCCCACCTCAGCCTCCCGGGTAGCTGGGACCACAGGTATGTGCCACTATGCCTGGCTAGTTTTG CTCCCACCTCAGCCTCCCGGGTAGCTGGGACCGCAGGTATGTGCCACTATGCCTGGCTAGTTTTG T C RF00017-4494 RNACentral:URS00009086DB SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1228782078 Functional Loss SNV dbSNP153 33..33 33 - - - 30715 RMVar_ID_30715 Human_SNP_ID_326185796 A-to-I Human chr7 + 74088027 74088027 74088027 GCTCCAACTGGTTCAAGCGATCCTTCTGACTCAGCCTCCCAAAGTGCTGGGATTACAAGCATAAG GCTCCAACTGGTTCAAGCGATCCTTCTGACTCGGCCTCCCAAAGTGCTGGGATTACAAGCATAAG A G LIMK1 Ensembl:ENSG00000106683 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1291119973 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110007,RMVar_hsa_circ_122578,RMVar_hsa_circ_245614,RMVar_hsa_circ_124213,RMVar_hsa_circ_245612,RMVar_hsa_circ_245613,RMVar_hsa_circ_374502,RMVar_hsa_circ_245615 30716 RMVar_ID_30716 Human_SNP_ID_326185802 A-to-I Human chr7 + 74088057 74088057 74088057 TCAGCCTCCCAAAGTGCTGGGATTACAAGCATAAGCCACCATGCCCAGCCTGTTTTTTCTTTTTT TCAGCCTCCCAAAGTGCTGGGATTACAAGCATCAGCCACCATGCCCAGCCTGTTTTTTCTTTTTT A C LIMK1 Ensembl:ENSG00000106683 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs543365854 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110007,RMVar_hsa_circ_122578,RMVar_hsa_circ_245614,RMVar_hsa_circ_124213,RMVar_hsa_circ_245612,RMVar_hsa_circ_245613,RMVar_hsa_circ_374502,RMVar_hsa_circ_245615 30717 RMVar_ID_30717 Human_SNP_ID_326185803 A-to-I Human chr7 + 74088057 74088057 74088057 TCAGCCTCCCAAAGTGCTGGGATTACAAGCATAAGCCACCATGCCCAGCCTGTTTTTTCTTTTTT TCAGCCTCCCAAAGTGCTGGGATTACAAGCATGAGCCACCATGCCCAGCCTGTTTTTTCTTTTTT A G LIMK1 Ensembl:ENSG00000106683 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs543365854 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110007,RMVar_hsa_circ_122578,RMVar_hsa_circ_245614,RMVar_hsa_circ_124213,RMVar_hsa_circ_245612,RMVar_hsa_circ_245613,RMVar_hsa_circ_374502,RMVar_hsa_circ_245615 30718 RMVar_ID_30718 Human_SNP_ID_326188900 A-to-I Human chr7 + 74099609 74099609 74099609 AAACGTAGCCAGGCATGGTAGTGTGTGCCTATAGTGCCAGCTGCTTGGGAGGCTGAGGCAGGAGA AAACGTAGCCAGGCATGGTAGTGTGTGCCTATGGTGCCAGCTGCTTGGGAGGCTGAGGCAGGAGA A G LIMK1 Ensembl:ENSG00000106683 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1338572657 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44230,RMVar_hsa_circ_110007,RMVar_hsa_circ_245614,RMVar_hsa_circ_124213,RMVar_hsa_circ_245613,RMVar_hsa_circ_374502,RMVar_hsa_circ_245615,RMVar_hsa_circ_369982,RMVar_hsa_circ_102293,RMVar_hsa_circ_98103,RMVar_hsa_circ_245618,RMVar_hsa_circ_245619,RMVar_hsa_circ_245621,RMVar_hsa_circ_88451,RMVar_hsa_circ_245622 30719 RMVar_ID_30719 Human_SNP_ID_326189289 A-to-I Human chr7 + 74101017 74101017 74101017 TCTCGGCCTCCCAAAGTGCTGCGATTACAGGCATGAGCCACCACGCCCGGCCCTACCAAGTGCTA TCTCGGCCTCCCAAAGTGCTGCGATTACAGGCGTGAGCCACCACGCCCGGCCCTACCAAGTGCTA A G LIMK1 Ensembl:ENSG00000106683 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1554696494 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44230,RMVar_hsa_circ_110007,RMVar_hsa_circ_245614,RMVar_hsa_circ_124213,RMVar_hsa_circ_245613,RMVar_hsa_circ_374502,RMVar_hsa_circ_245615,RMVar_hsa_circ_369982,RMVar_hsa_circ_102293,RMVar_hsa_circ_98103,RMVar_hsa_circ_245618,RMVar_hsa_circ_245619,RMVar_hsa_circ_245621,RMVar_hsa_circ_88451,RMVar_hsa_circ_245622 30720 RMVar_ID_30720 Human_SNP_ID_326190027 A-to-I Human chr7 + 74103894 74103894 74103894 ATAGCTCACTGCAGCCTCGACCTCATGGGCTCAAGCGATCCTCCTGCCTCAGCCTCTCGAGTAGC ATAGCTCACTGCAGCCTCGACCTCATGGGCTCGAGCGATCCTCCTGCCTCAGCCTCTCGAGTAGC A G LIMK1 Ensembl:ENSG00000106683 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1554696963 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44230,RMVar_hsa_circ_110007,RMVar_hsa_circ_245614,RMVar_hsa_circ_124213,RMVar_hsa_circ_245613,RMVar_hsa_circ_374502,RMVar_hsa_circ_245615,RMVar_hsa_circ_369982,RMVar_hsa_circ_102293,RMVar_hsa_circ_98103,RMVar_hsa_circ_245618,RMVar_hsa_circ_245619,RMVar_hsa_circ_245621,RMVar_hsa_circ_88451,RMVar_hsa_circ_245622 30721 RMVar_ID_30721 Human_SNP_ID_326190032 A-to-I Human chr7 + 74103912 74103912 74103912 GACCTCATGGGCTCAAGCGATCCTCCTGCCTCAGCCTCTCGAGTAGCTGGGACTACAGGCAGCAC GACCTCATGGGCTCAAGCGATCCTCCTGCCTCGGCCTCTCGAGTAGCTGGGACTACAGGCAGCAC A G LIMK1 Ensembl:ENSG00000106683 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1554696969 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44230,RMVar_hsa_circ_110007,RMVar_hsa_circ_245614,RMVar_hsa_circ_124213,RMVar_hsa_circ_245613,RMVar_hsa_circ_374502,RMVar_hsa_circ_245615,RMVar_hsa_circ_369982,RMVar_hsa_circ_102293,RMVar_hsa_circ_98103,RMVar_hsa_circ_245618,RMVar_hsa_circ_245619,RMVar_hsa_circ_245621,RMVar_hsa_circ_88451,RMVar_hsa_circ_245622 30722 RMVar_ID_30722 Human_SNP_ID_326190259 A-to-I Human chr7 + 74104937 74104937 74104937 TCTGCCCCAAGCATACCAGGCAGGCCAGGTGCAATGACTCATGTCTGTAATCCTAGCACTTTGTT TCTGCCCCAAGCATACCAGGCAGGCCAGGTGCCATGACTCATGTCTGTAATCCTAGCACTTTGTT A C LIMK1 Ensembl:ENSG00000106683 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1234854174 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44230,RMVar_hsa_circ_110007,RMVar_hsa_circ_245614,RMVar_hsa_circ_124213,RMVar_hsa_circ_245613,RMVar_hsa_circ_374502,RMVar_hsa_circ_245615,RMVar_hsa_circ_369982,RMVar_hsa_circ_102293,RMVar_hsa_circ_98103,RMVar_hsa_circ_245618,RMVar_hsa_circ_245619,RMVar_hsa_circ_245621,RMVar_hsa_circ_88451,RMVar_hsa_circ_245622 30723 RMVar_ID_30723 Human_SNP_ID_326190295 A-to-I Human chr7 + 74105079 74105079 74105079 CCAGGTTCAAGCAATTCCTGCCTCAGCCTCCCAAGTAGCTAGGACTACAGGCGCCCACTGCCACG CCAGGTTCAAGCAATTCCTGCCTCAGCCTCCCGAGTAGCTAGGACTACAGGCGCCCACTGCCACG A G LIMK1 Ensembl:ENSG00000106683 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs61068133 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44230,RMVar_hsa_circ_110007,RMVar_hsa_circ_245614,RMVar_hsa_circ_124213,RMVar_hsa_circ_245613,RMVar_hsa_circ_374502,RMVar_hsa_circ_245615,RMVar_hsa_circ_369982,RMVar_hsa_circ_102293,RMVar_hsa_circ_98103,RMVar_hsa_circ_245618,RMVar_hsa_circ_245619,RMVar_hsa_circ_245621,RMVar_hsa_circ_88451,RMVar_hsa_circ_245622 30724 RMVar_ID_30724 Human_SNP_ID_326190297 A-to-I Human chr7 + 74105083 74105083 74105083 GTTCAAGCAATTCCTGCCTCAGCCTCCCAAGTAGCTAGGACTACAGGCGCCCACTGCCACGCTCG GTTCAAGCAATTCCTGCCTCAGCCTCCCAAGTGGCTAGGACTACAGGCGCCCACTGCCACGCTCG A G LIMK1 Ensembl:ENSG00000106683 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs534748410 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44230,RMVar_hsa_circ_110007,RMVar_hsa_circ_245614,RMVar_hsa_circ_124213,RMVar_hsa_circ_245613,RMVar_hsa_circ_374502,RMVar_hsa_circ_245615,RMVar_hsa_circ_369982,RMVar_hsa_circ_102293,RMVar_hsa_circ_98103,RMVar_hsa_circ_245618,RMVar_hsa_circ_245619,RMVar_hsa_circ_245621,RMVar_hsa_circ_88451,RMVar_hsa_circ_245622 30725 RMVar_ID_30725 Human_SNP_ID_326190328 A-to-I Human chr7 + 74105192 74105192 74105192 GCCAGGCTGGTCTCAAACTCCTGACTTCAAGTAATCCATCCACCTTGGCCTCCCCAACTGTTGGG GCCAGGCTGGTCTCAAACTCCTGACTTCAAGTGATCCATCCACCTTGGCCTCCCCAACTGTTGGG A G LIMK1 Ensembl:ENSG00000106683 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1211826442 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44230,RMVar_hsa_circ_110007,RMVar_hsa_circ_245614,RMVar_hsa_circ_124213,RMVar_hsa_circ_245613,RMVar_hsa_circ_374502,RMVar_hsa_circ_245615,RMVar_hsa_circ_369982,RMVar_hsa_circ_102293,RMVar_hsa_circ_98103,RMVar_hsa_circ_245618,RMVar_hsa_circ_245619,RMVar_hsa_circ_245621,RMVar_hsa_circ_88451,RMVar_hsa_circ_245622 30726 RMVar_ID_30726 Human_SNP_ID_326190373 A-to-I Human chr7 + 74105366 74105366 74105366 ACCCCGTCTCTACTAAAAATACAAAAAAAATTAGCTGGGTGTGGTGGTGTGCACCTGTAATCCCA ACCCCGTCTCTACTAAAAATACAAAAAAAATTGGCTGGGTGTGGTGGTGTGCACCTGTAATCCCA A G LIMK1 Ensembl:ENSG00000106683 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs757898470 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44230,RMVar_hsa_circ_110007,RMVar_hsa_circ_245614,RMVar_hsa_circ_124213,RMVar_hsa_circ_245613,RMVar_hsa_circ_374502,RMVar_hsa_circ_245615,RMVar_hsa_circ_369982,RMVar_hsa_circ_102293,RMVar_hsa_circ_98103,RMVar_hsa_circ_245618,RMVar_hsa_circ_245619,RMVar_hsa_circ_245621,RMVar_hsa_circ_88451,RMVar_hsa_circ_245622 30727 RMVar_ID_30727 Human_SNP_ID_326190379 A-to-I Human chr7 + 74105402 74105402 74105402 GGGTGTGGTGGTGTGCACCTGTAATCCCAGCTACTCAGGAGGCTGAGGTACGAGAATCGCTTGAA GGGTGTGGTGGTGTGCACCTGTAATCCCAGCTGCTCAGGAGGCTGAGGTACGAGAATCGCTTGAA A G LIMK1 Ensembl:ENSG00000106683 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1197397468 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44230,RMVar_hsa_circ_110007,RMVar_hsa_circ_245614,RMVar_hsa_circ_124213,RMVar_hsa_circ_245613,RMVar_hsa_circ_374502,RMVar_hsa_circ_245615,RMVar_hsa_circ_369982,RMVar_hsa_circ_102293,RMVar_hsa_circ_98103,RMVar_hsa_circ_245618,RMVar_hsa_circ_245619,RMVar_hsa_circ_245621,RMVar_hsa_circ_88451,RMVar_hsa_circ_245622 30728 RMVar_ID_30728 Human_SNP_ID_326190381 A-to-I Human chr7 + 74105406 74105406 74105406 GTGGTGGTGTGCACCTGTAATCCCAGCTACTCAGGAGGCTGAGGTACGAGAATCGCTTGAACTCA GTGGTGGTGTGCACCTGTAATCCCAGCTACTCGGGAGGCTGAGGTACGAGAATCGCTTGAACTCA A G LIMK1 Ensembl:ENSG00000106683 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1479978155 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44230,RMVar_hsa_circ_110007,RMVar_hsa_circ_245614,RMVar_hsa_circ_124213,RMVar_hsa_circ_245613,RMVar_hsa_circ_374502,RMVar_hsa_circ_245615,RMVar_hsa_circ_369982,RMVar_hsa_circ_102293,RMVar_hsa_circ_98103,RMVar_hsa_circ_245618,RMVar_hsa_circ_245619,RMVar_hsa_circ_245621,RMVar_hsa_circ_88451,RMVar_hsa_circ_245622 30729 RMVar_ID_30729 Human_SNP_ID_326191668 A-to-I Human chr7 + 74109724 74109724 74109724 AAAATTAGCCGGGCAAGGTGGCAGGTGCCTGTAGTCCCAGCTACTCGGGAGACTGAAGCAGGAGA AAAATTAGCCGGGCAAGGTGGCAGGTGCCTGTGGTCCCAGCTACTCGGGAGACTGAAGCAGGAGA A G LIMK1 Ensembl:ENSG00000106683 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1474702607 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25378,RMVar_hsa_circ_124213,RMVar_hsa_circ_245615,RMVar_hsa_circ_369982,RMVar_hsa_circ_102293,RMVar_hsa_circ_98103,RMVar_hsa_circ_245618,RMVar_hsa_circ_245619,RMVar_hsa_circ_84925,RMVar_hsa_circ_245622,RMVar_hsa_circ_313114,RMVar_hsa_circ_105840,RMVar_hsa_circ_245624,RMVar_hsa_circ_365489,RMVar_hsa_circ_245626 30730 RMVar_ID_30730 Human_SNP_ID_326191917 A-to-I Human chr7 + 74110711 74110711 74110711 CACCACCACACCCGGCTAATTTTTGCGTTTTTAGTAGAGACAGGGTTTCACCATGTTGGTCAGGC CACCACCACACCCGGCTAATTTTTGCGTTTTTGGTAGAGACAGGGTTTCACCATGTTGGTCAGGC A G LIMK1 Ensembl:ENSG00000106683 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs564375628 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_174366 RMVar_hsa_circ_25378,RMVar_hsa_circ_124213,RMVar_hsa_circ_245615,RMVar_hsa_circ_369982,RMVar_hsa_circ_102293,RMVar_hsa_circ_98103,RMVar_hsa_circ_245618,RMVar_hsa_circ_245619,RMVar_hsa_circ_84925,RMVar_hsa_circ_245622,RMVar_hsa_circ_313114,RMVar_hsa_circ_105840,RMVar_hsa_circ_245624,RMVar_hsa_circ_365489,RMVar_hsa_circ_245626 30731 RMVar_ID_30731 Human_SNP_ID_326191918 A-to-I Human chr7 + 74110720 74110720 74110720 ACCCGGCTAATTTTTGCGTTTTTAGTAGAGACAGGGTTTCACCATGTTGGTCAGGCTGGTCTCAA ACCCGGCTAATTTTTGCGTTTTTAGTAGAGACGGGGTTTCACCATGTTGGTCAGGCTGGTCTCAA A G LIMK1 Ensembl:ENSG00000106683 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs201114657 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_174366 RMVar_hsa_circ_25378,RMVar_hsa_circ_124213,RMVar_hsa_circ_245615,RMVar_hsa_circ_369982,RMVar_hsa_circ_102293,RMVar_hsa_circ_98103,RMVar_hsa_circ_245618,RMVar_hsa_circ_245619,RMVar_hsa_circ_84925,RMVar_hsa_circ_245622,RMVar_hsa_circ_313114,RMVar_hsa_circ_105840,RMVar_hsa_circ_245624,RMVar_hsa_circ_365489,RMVar_hsa_circ_245626 30732 RMVar_ID_30732 Human_SNP_ID_326193463 A-to-I Human chr7 + 74116512 74116512 74116512 TCCAGCGTCAGCCTCACCGGGCTGAAATCAAGACGCCGGTAGGGTGAGCTCCTTCTGCAGGCTCC TCCAGCGTCAGCCTCACCGGGCTGAAATCAAGGCGCCGGTAGGGTGAGCTCCTTCTGCAGGCTCC A G LIMK1 Ensembl:ENSG00000106683 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs178408 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124213,RMVar_hsa_circ_245615,RMVar_hsa_circ_98103,RMVar_hsa_circ_84925,RMVar_hsa_circ_245622,RMVar_hsa_circ_105840,RMVar_hsa_circ_245624,RMVar_hsa_circ_22980,RMVar_hsa_circ_245626 30733 RMVar_ID_30733 Human_SNP_ID_326193681 A-to-I Human chr7 + 74117212 74117212 74117212 CAATTTTTTAAATTTTTAATAGAGACGGGGGTATCACTATGTTGCCCAGGCTGGTCTCAAACTCC CAATTTTTTAAATTTTTAATAGAGACGGGGGTGTCACTATGTTGCCCAGGCTGGTCTCAAACTCC A G LIMK1 Ensembl:ENSG00000106683 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1194882738 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124213,RMVar_hsa_circ_245615,RMVar_hsa_circ_98103,RMVar_hsa_circ_84925,RMVar_hsa_circ_245622,RMVar_hsa_circ_105840,RMVar_hsa_circ_245624,RMVar_hsa_circ_22980,RMVar_hsa_circ_245626 30734 RMVar_ID_30734 Human_SNP_ID_326210007 A-to-I Human chr7 + 74178015 74178015 74178015 CAGGCTGGAGTGCAGTGGCAGGATCATAGCTCAGTGCAGCCTCGACTTCCCAGGCTCAAGCCATC CAGGCTGGAGTGCAGTGGCAGGATCATAGCTCGGTGCAGCCTCGACTTCCCAGGCTCAAGCCATC A G EIF4H Ensembl:ENSG00000106682 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs938196420 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99960,RMVar_hsa_circ_245630 30735 RMVar_ID_30735 Human_SNP_ID_326210049 A-to-I Human chr7 + 74178155 74178155 74178155 TAGAGACAGAGTGTCTCTATGTTGCCCAGGCTAGTCTCAAACCCCTGGGCTCAAGGGATCTTCCT TAGAGACAGAGTGTCTCTATGTTGCCCAGGCTCGTCTCAAACCCCTGGGCTCAAGGGATCTTCCT A C EIF4H Ensembl:ENSG00000106682 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs983164805 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17577170 RMVar_hsa_circ_99960,RMVar_hsa_circ_245630 30736 RMVar_ID_30736 Human_SNP_ID_326210050 A-to-I Human chr7 + 74178155 74178155 74178155 TAGAGACAGAGTGTCTCTATGTTGCCCAGGCTAGTCTCAAACCCCTGGGCTCAAGGGATCTTCCT TAGAGACAGAGTGTCTCTATGTTGCCCAGGCTGGTCTCAAACCCCTGGGCTCAAGGGATCTTCCT A G EIF4H Ensembl:ENSG00000106682 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs983164805 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17577170 RMVar_hsa_circ_99960,RMVar_hsa_circ_245630 30737 RMVar_ID_30737 Human_SNP_ID_326210101 A-to-I Human chr7 + 74178360 74178360 74178360 TCACTTGTGGCCAGAAGTTTGAGACCACCCTGACCAACGTGGCAAAACCCCATGTCTACTAAAAA TCACTTGTGGCCAGAAGTTTGAGACCACCCTGGCCAACGTGGCAAAACCCCATGTCTACTAAAAA A G EIF4H Ensembl:ENSG00000106682 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs150878 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_3414,GWAS_ID_3415,GWAS_ID_3416,GWAS_ID_3417,GWAS_ID_3418,GWAS_ID_3419,GWAS_ID_3420 RMVar_hsa_circ_99960,RMVar_hsa_circ_245630 30738 RMVar_ID_30738 Human_SNP_ID_326211061 A-to-I Human chr7 + 74181967 74181967 74181967 TTGAACTCCTGACCTTGTGATTCATCCGCTTCAGCCTCCCAAAGTGCTGGGATTATAGGTGTGAG TTGAACTCCTGACCTTGTGATTCATCCGCTTCGGCCTCCCAAAGTGCTGGGATTATAGGTGTGAG A G EIF4H Ensembl:ENSG00000106682 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs550141686 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99960,RMVar_hsa_circ_245630 30739 RMVar_ID_30739 Human_SNP_ID_326212217 A-to-I Human chr7 + 74186379 74186379 74186379 GGGATTACAGGCATGCACCACCACACCAAGCTAATTTTGTATTTTTAGTAGAGACAGGGTTTTAC GGGATTACAGGCATGCACCACCACACCAAGCTGATTTTGTATTTTTAGTAGAGACAGGGTTTTAC A G EIF4H Ensembl:ENSG00000106682 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs992027629 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99960,RMVar_hsa_circ_245630 30740 RMVar_ID_30740 Human_SNP_ID_326219228 A-to-I Human chr7 + 74210738 74210738 74210738 GGGAGGCCAAGGCGGGAGGATCATTTGAAGTCAGGAGCTGGAGACCAGCCTGAGCAACATAGTGA GGGAGGCCAAGGCGGGAGGATCATTTGAAGTCTGGAGCTGGAGACCAGCCTGAGCAACATAGTGA A T LAT2 Ensembl:ENSG00000086730 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs181565078 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106046,RMVar_hsa_circ_245636 30741 RMVar_ID_30741 Human_SNP_ID_326221884 A-to-I Human chr7 + 74217270 74217270 74217270 CCTGGCCAACATGGTGAAACCTCATTTCTACTAAAATACAAAAATGAGCTGGGCGTGGTGGTGGG CCTGGCCAACATGGTGAAACCTCATTTCTACTCAAATACAAAAATGAGCTGGGCGTGGTGGTGGG A C LAT2 Ensembl:ENSG00000086730 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1554714412 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83146,RMVar_hsa_circ_106046,RMVar_hsa_circ_101450,RMVar_hsa_circ_245636,RMVar_hsa_circ_245637,RMVar_hsa_circ_245638,RMVar_hsa_circ_75571,RMVar_hsa_circ_245640 30742 RMVar_ID_30742 Human_SNP_ID_326222297 A-to-I Human chr7 + 74218972 74218972 74218972 CGCCTGCCTTGGCCTCCCAAAGCCCTGGGATTACAGGTGTGAGCCACCATGCCGGGTCTAGAGTG CGCCTGCCTTGGCCTCCCAAAGCCCTGGGATTGCAGGTGTGAGCCACCATGCCGGGTCTAGAGTG A G LAT2 Ensembl:ENSG00000086730 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1322667301 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83146,RMVar_hsa_circ_106046,RMVar_hsa_circ_101450,RMVar_hsa_circ_245636,RMVar_hsa_circ_245637,RMVar_hsa_circ_245638,RMVar_hsa_circ_75571,RMVar_hsa_circ_245640 30743 RMVar_ID_30743 Human_SNP_ID_326224984 A-to-I Human chr7 - 74227307 74227307 74227307 GCTGAGGCAAGAGAAACCTGAACCCAGGAGGCAGAGGTTGCAGTGAGCCGAGATCACGCCACTGC GCTGAGGCAAGAGAAACCTGAACCCAGGAGGCGGAGGTTGCAGTGAGCCGAGATCACGCCACTGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1280801409 Functional Loss SNV dbSNP153 33..33 33 - - - 30744 RMVar_ID_30744 Human_SNP_ID_326226209 A-to-I Human chr7 - 74231899 74231899 74231899 GAGGCAGGTGGATCACCTGAGGTCAGAAGTTCAAGACCAGCCTGGCCAACATGGGGAAACCCTGT GAGGCAGGTGGATCACCTGAGGTCAGAAGTTCGAGACCAGCCTGGCCAACATGGGGAAACCCTGT T C RFC2 Ensembl:ENSG00000049541 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1134216 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1266222,Human_miRNA_ID_1691037 RMVar_hsa_circ_245644,RMVar_hsa_circ_90739 30745 RMVar_ID_30745 Human_SNP_ID_326226210 A-to-I Human chr7 - 74231899 74231899 74231899 GAGGCAGGTGGATCACCTGAGGTCAGAAGTTCAAGACCAGCCTGGCCAACATGGGGAAACCCTGT GAGGCAGGTGGATCACCTGAGGTCAGAAGTTCCAGACCAGCCTGGCCAACATGGGGAAACCCTGT T G RFC2 Ensembl:ENSG00000049541 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1134216 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1266222,Human_miRNA_ID_1691037 RMVar_hsa_circ_245644,RMVar_hsa_circ_90739 30746 RMVar_ID_30746 Human_SNP_ID_326228361 A-to-I Human chr7 - 74240339 74240339 74240339 CGACACCACACCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGTCCAGGC CGACACCACACCCAGCTAATTTTTGTATTTTTGGTAGAGATGGGGTTTCACCATGTTGTCCAGGC T C RFC2 Ensembl:ENSG00000049541 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs782144235 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8320,RMVar_hsa_circ_245647,RMVar_hsa_circ_346844,RMVar_hsa_circ_46994,RMVar_hsa_circ_291011,RMVar_hsa_circ_9055,RMVar_hsa_circ_245654,RMVar_hsa_circ_116375,RMVar_hsa_circ_245650,RMVar_hsa_circ_67669,RMVar_hsa_circ_294357,RMVar_hsa_circ_118181,RMVar_hsa_circ_281736,RMVar_hsa_circ_305210,RMVar_hsa_circ_245652,RMVar_hsa_circ_315698,RMVar_hsa_circ_289374,RMVar_hsa_circ_276551,RMVar_hsa_circ_245656,RMVar_hsa_circ_17742,RMVar_hsa_circ_245657,RMVar_hsa_circ_245655,RMVar_hsa_circ_245653 30747 RMVar_ID_30747 Human_SNP_ID_326228374 A-to-I Human chr7 - 74240386 74240386 74240386 GCGAGTCTCTTGCCTTAGCCTCCTGAGTAGCTAGGATTACAGACGTGCGACACCACACCCAGCTA GCGAGTCTCTTGCCTTAGCCTCCTGAGTAGCTGGGATTACAGACGTGCGACACCACACCCAGCTA T C RFC2 Ensembl:ENSG00000049541 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs79019161 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8320,RMVar_hsa_circ_245647,RMVar_hsa_circ_346844,RMVar_hsa_circ_46994,RMVar_hsa_circ_291011,RMVar_hsa_circ_9055,RMVar_hsa_circ_245654,RMVar_hsa_circ_116375,RMVar_hsa_circ_245650,RMVar_hsa_circ_67669,RMVar_hsa_circ_294357,RMVar_hsa_circ_118181,RMVar_hsa_circ_281736,RMVar_hsa_circ_305210,RMVar_hsa_circ_245652,RMVar_hsa_circ_315698,RMVar_hsa_circ_289374,RMVar_hsa_circ_276551,RMVar_hsa_circ_245656,RMVar_hsa_circ_17742,RMVar_hsa_circ_245657,RMVar_hsa_circ_245655,RMVar_hsa_circ_245653 30748 RMVar_ID_30748 Human_SNP_ID_326229886 A-to-I Human chr7 - 74246074 74246074 74246074 CTCCTGCCTCAGCCTCCCGAGTAGCTGAGACTACAGGCATGCACCACCACGCCCAGCTGATTTTT CTCCTGCCTCAGCCTCCCGAGTAGCTGAGACTGCAGGCATGCACCACCACGCCCAGCTGATTTTT T C RFC2 Ensembl:ENSG00000049541 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1333351728 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8320,RMVar_hsa_circ_245647,RMVar_hsa_circ_346844,RMVar_hsa_circ_46994,RMVar_hsa_circ_291011,RMVar_hsa_circ_245654,RMVar_hsa_circ_116375,RMVar_hsa_circ_245650,RMVar_hsa_circ_67669,RMVar_hsa_circ_294357,RMVar_hsa_circ_118181,RMVar_hsa_circ_305210,RMVar_hsa_circ_245652,RMVar_hsa_circ_315698,RMVar_hsa_circ_289374,RMVar_hsa_circ_276551,RMVar_hsa_circ_245656,RMVar_hsa_circ_17742,RMVar_hsa_circ_245655,RMVar_hsa_circ_245659,RMVar_hsa_circ_20589,RMVar_hsa_circ_293509,RMVar_hsa_circ_245653,RMVar_hsa_circ_372257,RMVar_hsa_circ_265389,RMVar_hsa_circ_245660 30749 RMVar_ID_30749 Human_SNP_ID_326229970 A-to-I Human chr7 - 74246336 74246336 74246336 GGAGTATAGTGGTGTGATCTCTGCTCACTGCAACCTCCGCCTCCCGGGTTCAGGCGGTTCCCTGG GGAGTATAGTGGTGTGATCTCTGCTCACTGCAGCCTCCGCCTCCCGGGTTCAGGCGGTTCCCTGG T C RFC2 Ensembl:ENSG00000049541 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1298861017 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16215905 RMVar_hsa_circ_8320,RMVar_hsa_circ_245647,RMVar_hsa_circ_346844,RMVar_hsa_circ_46994,RMVar_hsa_circ_291011,RMVar_hsa_circ_245654,RMVar_hsa_circ_116375,RMVar_hsa_circ_245650,RMVar_hsa_circ_67669,RMVar_hsa_circ_294357,RMVar_hsa_circ_118181,RMVar_hsa_circ_305210,RMVar_hsa_circ_245652,RMVar_hsa_circ_315698,RMVar_hsa_circ_289374,RMVar_hsa_circ_276551,RMVar_hsa_circ_245656,RMVar_hsa_circ_17742,RMVar_hsa_circ_245655,RMVar_hsa_circ_245659,RMVar_hsa_circ_20589,RMVar_hsa_circ_293509,RMVar_hsa_circ_245653,RMVar_hsa_circ_372257,RMVar_hsa_circ_265389,RMVar_hsa_circ_245660 30750 RMVar_ID_30750 Human_SNP_ID_326230284 A-to-I Human chr7 - 74247474 74247474 74247474 GGGCACGCCCAGGTAATTTTTGTATTTTTAGTAAAGATGGATTTTCGCCGTGTTGGCCAGGTTGA GGGCACGCCCAGGTAATTTTTGTATTTTTAGTGAAGATGGATTTTCGCCGTGTTGGCCAGGTTGA T C RFC2 Ensembl:ENSG00000049541 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1226731448 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8320,RMVar_hsa_circ_346844,RMVar_hsa_circ_46994,RMVar_hsa_circ_245654,RMVar_hsa_circ_116375,RMVar_hsa_circ_67669,RMVar_hsa_circ_118181,RMVar_hsa_circ_305210,RMVar_hsa_circ_245652,RMVar_hsa_circ_315698,RMVar_hsa_circ_289374,RMVar_hsa_circ_17742,RMVar_hsa_circ_245655,RMVar_hsa_circ_20589,RMVar_hsa_circ_245653,RMVar_hsa_circ_372257,RMVar_hsa_circ_265389,RMVar_hsa_circ_245660 30751 RMVar_ID_30751 Human_SNP_ID_326230332 A-to-I Human chr7 - 74247634 74247633 74247635 TGTTCTTTTCTTTCTTTCTTTTTTTTTGAGACAGAGTCTTGCTCTGTCACCCAGGCTGGAGTGCA TGTTCTTTTCTTTCTTTCTTTTTTTTTGAGA__GAGTCTTGCTCTGTCACCCAGGCTGGAGTGCA CTG C RFC2 Ensembl:ENSG00000049541 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1554720289 Functional Loss DEL dbSNP153 32..33 33 - - - Human_miRNA_ID_2877062,Human_miRNA_ID_2877063 RMVar_hsa_circ_8320,RMVar_hsa_circ_346844,RMVar_hsa_circ_46994,RMVar_hsa_circ_245654,RMVar_hsa_circ_116375,RMVar_hsa_circ_67669,RMVar_hsa_circ_118181,RMVar_hsa_circ_305210,RMVar_hsa_circ_245652,RMVar_hsa_circ_315698,RMVar_hsa_circ_289374,RMVar_hsa_circ_17742,RMVar_hsa_circ_245655,RMVar_hsa_circ_20589,RMVar_hsa_circ_245653,RMVar_hsa_circ_372257,RMVar_hsa_circ_265389,RMVar_hsa_circ_245660 30752 RMVar_ID_30752 Human_SNP_ID_326230482 A-to-I Human chr7 - 74248287 74248287 74248287 TTGCCCAGTCTGGTCTCGAACTCCGGGACTCAAGCGATCCTCCTTGCATCAGCCTCCCAAAGTGC TTGCCCAGTCTGGTCTCGAACTCCGGGACTCAGGCGATCCTCCTTGCATCAGCCTCCCAAAGTGC T C RFC2 Ensembl:ENSG00000049541 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1242655116 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8320,RMVar_hsa_circ_346844,RMVar_hsa_circ_46994,RMVar_hsa_circ_245654,RMVar_hsa_circ_116375,RMVar_hsa_circ_67669,RMVar_hsa_circ_118181,RMVar_hsa_circ_305210,RMVar_hsa_circ_245652,RMVar_hsa_circ_315698,RMVar_hsa_circ_289374,RMVar_hsa_circ_17742,RMVar_hsa_circ_245655,RMVar_hsa_circ_20589,RMVar_hsa_circ_245653,RMVar_hsa_circ_372257,RMVar_hsa_circ_265389,RMVar_hsa_circ_245660 30753 RMVar_ID_30753 Human_SNP_ID_326230488 A-to-I Human chr7 - 74248313 74248313 74248313 TCTTGTGGAGACGGGATCTCACTATGTTGCCCAGTCTGGTCTCGAACTCCGGGACTCAAGCGATC TCTTGTGGAGACGGGATCTCACTATGTTGCCCGGTCTGGTCTCGAACTCCGGGACTCAAGCGATC T C RFC2 Ensembl:ENSG00000049541 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs755688161 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8320,RMVar_hsa_circ_346844,RMVar_hsa_circ_46994,RMVar_hsa_circ_245654,RMVar_hsa_circ_116375,RMVar_hsa_circ_67669,RMVar_hsa_circ_118181,RMVar_hsa_circ_305210,RMVar_hsa_circ_245652,RMVar_hsa_circ_315698,RMVar_hsa_circ_289374,RMVar_hsa_circ_17742,RMVar_hsa_circ_245655,RMVar_hsa_circ_20589,RMVar_hsa_circ_245653,RMVar_hsa_circ_372257,RMVar_hsa_circ_265389,RMVar_hsa_circ_245660 30754 RMVar_ID_30754 Human_SNP_ID_326231383 A-to-I Human chr7 - 74251463 74251463 74251463 ACCTAAGGCTGGGCACAGTGGCTTACACCTGTAATCCCAGCACCTTGGGAGGCTAAGGCGGGCAG ACCTAAGGCTGGGCACAGTGGCTTACACCTGTGATCCCAGCACCTTGGGAGGCTAAGGCGGGCAG T C RFC2 Ensembl:ENSG00000049541 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1328166668 Functional Loss SNV dbSNP153 33..33 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 30755 RMVar_ID_30755 Human_SNP_ID_326237967 A-to-I Human chr7 - 74275205 74275205 74275205 CATGGTGGTGTGTGCCTGTAGTCCCAGCTACTAGGGAGGCTGAGGCAGGGGAATCGCTTGACCCT CATGGTGGTGTGTGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGGGAATCGCTTGACCCT T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1378409304 Functional Loss SNV dbSNP153 33..33 33 - - - 30756 RMVar_ID_30756 Human_SNP_ID_326247168 A-to-I Human chr7 + 74309069 74309069 74309069 TTTGTATTATTTTGTAGAGATAGATTTTCGCCATGTTGCCCAGGCTGGTCTCAAACTCCTGAGCT TTTGTATTATTTTGTAGAGATAGATTTTCGCCGTGTTGCCCAGGCTGGTCTCAAACTCCTGAGCT A G CLIP2 Ensembl:ENSG00000106665 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1554728125 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_245663,RMVar_hsa_circ_92919,RMVar_hsa_circ_245662 30757 RMVar_ID_30757 Human_SNP_ID_326262530 A-to-I Human chr7 + 74366052 74366052 74366052 ATCCTGCCTCAGCCTCCCAAAGGGCTGGGATTACATGCATGAGCCATCACATCTGGCCCCCACCC ATCCTGCCTCAGCCTCCCAAAGGGCTGGGATTGCATGCATGAGCCATCACATCTGGCCCCCACCC A G CLIP2 Ensembl:ENSG00000106665 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1479165375 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107546,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 30758 RMVar_ID_30758 Human_SNP_ID_326262677 A-to-I Human chr7 + 74366755 74366755 74366755 AAAATTAGCTGGGCATGGTGACGGGCGCCTCTAATCCCAGCTACTCCGGAGGCTGAGGCAGGAGA AAAATTAGCTGGGCATGGTGACGGGCGCCTCTTATCCCAGCTACTCCGGAGGCTGAGGCAGGAGA A T CLIP2 Ensembl:ENSG00000106665 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1554310922 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107546,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 30759 RMVar_ID_30759 Human_SNP_ID_326262940 A-to-I Human chr7 + 74367821 74367821 74367821 ACAGTTGGCTGGGCATGGTGGCTCACACCTGTAATCCCAGTGCTTTGGGAGCCTGAGACAGGAAG ACAGTTGGCTGGGCATGGTGGCTCACACCTGTGATCCCAGTGCTTTGGGAGCCTGAGACAGGAAG A G CLIP2 Ensembl:ENSG00000106665 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1419561351 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107546,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 30760 RMVar_ID_30760 Human_SNP_ID_326262965 A-to-I Human chr7 + 74367957 74367957 74367957 TTAAAAATGCGGGCATGGTGGCACATGCTTGTAATCCAAGCACTTTGGGAAGCCAAGGCGGGAGG TTAAAAATGCGGGCATGGTGGCACATGCTTGTCATCCAAGCACTTTGGGAAGCCAAGGCGGGAGG A C CLIP2 Ensembl:ENSG00000106665 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1455570027 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107546,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 30761 RMVar_ID_30761 Human_SNP_ID_326262996 A-to-I Human chr7 + 74368090 74368090 74368090 GAAAAATTATCCAGGTATGGTAATGCATGCCTATGGTCCCAGCTACGCGGGAGGTTGAGGTGGGA GAAAAATTATCCAGGTATGGTAATGCATGCCTGTGGTCCCAGCTACGCGGGAGGTTGAGGTGGGA A G CLIP2 Ensembl:ENSG00000106665 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs540774100 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107546,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 30762 RMVar_ID_30762 Human_SNP_ID_326266147 A-to-I Human chr7 + 74378482 74378482 74378482 GAATTTAGGGGTGGGTGTGGTGGCTCACACCTATAATTCCAGCATTTCGAGAGGCTGAGGCAGGA GAATTTAGGGGTGGGTGTGGTGGCTCACACCTCTAATTCCAGCATTTCGAGAGGCTGAGGCAGGA A C CLIP2 Ensembl:ENSG00000106665 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs192946052 Functional Loss SNV dbSNP153 33..33 33 - - - 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_245670,RMVar_hsa_circ_245684,RMVar_hsa_circ_80587,RMVar_hsa_circ_88021,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_313787,RMVar_hsa_circ_245694 30763 RMVar_ID_30763 Human_SNP_ID_326266148 A-to-I Human chr7 + 74378482 74378482 74378482 GAATTTAGGGGTGGGTGTGGTGGCTCACACCTATAATTCCAGCATTTCGAGAGGCTGAGGCAGGA GAATTTAGGGGTGGGTGTGGTGGCTCACACCTGTAATTCCAGCATTTCGAGAGGCTGAGGCAGGA A G CLIP2 Ensembl:ENSG00000106665 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs192946052 Functional Loss SNV dbSNP153 33..33 33 - - - 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_245670,RMVar_hsa_circ_245684,RMVar_hsa_circ_80587,RMVar_hsa_circ_88021,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_313787,RMVar_hsa_circ_245694 30764 RMVar_ID_30764 Human_SNP_ID_326266169 A-to-I Human chr7 + 74378558 74378558 74378558 GGCCAGGAGTTTGAGACCAGCCTGGACAACATAGTTAGACCCCATCTCTACAAAAATAAAAAATT GGCCAGGAGTTTGAGACCAGCCTGGACAACATGGTTAGACCCCATCTCTACAAAAATAAAAAATT A G CLIP2 Ensembl:ENSG00000106665 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs782500658 Functional Loss SNV dbSNP153 33..33 33 - - - 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_245670,RMVar_hsa_circ_245684,RMVar_hsa_circ_80587,RMVar_hsa_circ_88021,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_313787,RMVar_hsa_circ_245694 30765 RMVar_ID_30765 Human_SNP_ID_326266175 A-to-I Human chr7 + 74378591 74378591 74378591 GTTAGACCCCATCTCTACAAAAATAAAAAATTAGCCGAGTACAGTGGTAGTGTACCTGTAGTCCC GTTAGACCCCATCTCTACAAAAATAAAAAATTGGCCGAGTACAGTGGTAGTGTACCTGTAGTCCC A G CLIP2 Ensembl:ENSG00000106665 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1484885126 Functional Loss SNV dbSNP153 33..33 33 - - - 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_245670,RMVar_hsa_circ_245684,RMVar_hsa_circ_80587,RMVar_hsa_circ_88021,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_313787,RMVar_hsa_circ_245694 30766 RMVar_ID_30766 Human_SNP_ID_326266193 A-to-I Human chr7 + 74378665 74378665 74378665 TGGAGGCTGAGGCAAGAGGATCACTTGAGCCCAGGTGTTTGAGGCTGCAGTGAGCTATGATTGCA TGGAGGCTGAGGCAAGAGGATCACTTGAGCCCCGGTGTTTGAGGCTGCAGTGAGCTATGATTGCA A C CLIP2 Ensembl:ENSG00000106665 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs544697895 Functional Loss SNV dbSNP153 33..33 33 - - - 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_245670,RMVar_hsa_circ_245684,RMVar_hsa_circ_80587,RMVar_hsa_circ_88021,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_313787,RMVar_hsa_circ_245694 30767 RMVar_ID_30767 Human_SNP_ID_326266199 A-to-I Human chr7 + 74378716 74378716 74378716 GAGCTATGATTGCACCACTGCACTCCAGCCTGAGTGACAGTGTGAGGCTGTGACTCAAGAAAATA GAGCTATGATTGCACCACTGCACTCCAGCCTGGGTGACAGTGTGAGGCTGTGACTCAAGAAAATA A G CLIP2 Ensembl:ENSG00000106665 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1554313425 Functional Loss SNV dbSNP153 33..33 33 - - - 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_245670,RMVar_hsa_circ_245684,RMVar_hsa_circ_80587,RMVar_hsa_circ_88021,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_313787,RMVar_hsa_circ_245694 30768 RMVar_ID_30768 Human_SNP_ID_326267228 A-to-I Human chr7 + 74382957 74382957 74382957 CAAAAATTAGCCAGGTATGGTGGCATGCAGCTATAGTCCCAGATACTTGGGAAGGTGAGGCGGGA CAAAAATTAGCCAGGTATGGTGGCATGCAGCTGTAGTCCCAGATACTTGGGAAGGTGAGGCGGGA A G CLIP2 Ensembl:ENSG00000106665 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs536101018 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107546,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_245670,RMVar_hsa_circ_245684,RMVar_hsa_circ_80587,RMVar_hsa_circ_88021,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_7588,RMVar_hsa_circ_52305,RMVar_hsa_circ_310263,RMVar_hsa_circ_366751,RMVar_hsa_circ_302790,RMVar_hsa_circ_40225,RMVar_hsa_circ_245696 30769 RMVar_ID_30769 Human_SNP_ID_326267390 A-to-I Human chr7 + 74383719 74383719 74383719 CTCATGGGCTGGATTTGGTGGCTTACACCTGTAATTCCAGCACTTTGGGAGGCCCGGGCAGGAGA CTCATGGGCTGGATTTGGTGGCTTACACCTGTGATTCCAGCACTTTGGGAGGCCCGGGCAGGAGA A G CLIP2 Ensembl:ENSG00000106665 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs782029829 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107546,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_245670,RMVar_hsa_circ_245684,RMVar_hsa_circ_80587,RMVar_hsa_circ_88021,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_7588,RMVar_hsa_circ_52305,RMVar_hsa_circ_310263,RMVar_hsa_circ_366751,RMVar_hsa_circ_302790,RMVar_hsa_circ_40225,RMVar_hsa_circ_245696 30770 RMVar_ID_30770 Human_SNP_ID_326267391 A-to-I Human chr7 + 74383719 74383719 74383719 CTCATGGGCTGGATTTGGTGGCTTACACCTGTAATTCCAGCACTTTGGGAGGCCCGGGCAGGAGA CTCATGGGCTGGATTTGGTGGCTTACACCTGTTATTCCAGCACTTTGGGAGGCCCGGGCAGGAGA A T CLIP2 Ensembl:ENSG00000106665 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs782029829 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107546,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_245670,RMVar_hsa_circ_245684,RMVar_hsa_circ_80587,RMVar_hsa_circ_88021,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_7588,RMVar_hsa_circ_52305,RMVar_hsa_circ_310263,RMVar_hsa_circ_366751,RMVar_hsa_circ_302790,RMVar_hsa_circ_40225,RMVar_hsa_circ_245696 30771 RMVar_ID_30771 Human_SNP_ID_326267628 A-to-I Human chr7 + 74384685 74384685 74384685 CCAGACTGGTCTTGAACTCCTGGCCTCAATCGATGCACCTGCCTCGGCCTCCTGAAGTGCTGGGA CCAGACTGGTCTTGAACTCCTGGCCTCAATCGTTGCACCTGCCTCGGCCTCCTGAAGTGCTGGGA A T CLIP2 Ensembl:ENSG00000106665 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1395931272 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107546,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_245670,RMVar_hsa_circ_245684,RMVar_hsa_circ_80587,RMVar_hsa_circ_88021,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_7588,RMVar_hsa_circ_52305,RMVar_hsa_circ_310263,RMVar_hsa_circ_366751,RMVar_hsa_circ_302790,RMVar_hsa_circ_40225,RMVar_hsa_circ_245696 30772 RMVar_ID_30772 Human_SNP_ID_326268032 A-to-I Human chr7 + 74386103 74386102 74386103 CGAGTCTCGCTGTGTCGCCCAGGCTGGAGTGCAATGGCGCTATCTTGGCTTACTGCTGCCTCTGC CGAGTCTCGCTGTGTCGCCCAGGCTGGAGTGC_ATGGCGCTATCTTGGCTTACTGCTGCCTCTGC CA C CLIP2 Ensembl:ENSG00000106665 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1458736573 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_107546,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_245670,RMVar_hsa_circ_245684,RMVar_hsa_circ_80587,RMVar_hsa_circ_88021,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_7588,RMVar_hsa_circ_52305,RMVar_hsa_circ_310263,RMVar_hsa_circ_366751,RMVar_hsa_circ_302790,RMVar_hsa_circ_40225,RMVar_hsa_circ_245696 30773 RMVar_ID_30773 Human_SNP_ID_326268587 A-to-I Human chr7 + 74388198 74388198 74388198 CTAAAAATACAAAAAAATTAGCTGAGCGTGGTAGCGTGCACCTGTAGTCCCAGCTACTCAGGAGG CTAAAAATACAAAAAAATTAGCTGAGCGTGGTGGCGTGCACCTGTAGTCCCAGCTACTCAGGAGG A G CLIP2 Ensembl:ENSG00000106665 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1259981664 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118036,RMVar_hsa_circ_245671,RMVar_hsa_circ_88045,RMVar_hsa_circ_83371,RMVar_hsa_circ_245670,RMVar_hsa_circ_245684,RMVar_hsa_circ_80587,RMVar_hsa_circ_88021,RMVar_hsa_circ_245682,RMVar_hsa_circ_245683,RMVar_hsa_circ_84230,RMVar_hsa_circ_245690,RMVar_hsa_circ_65238,RMVar_hsa_circ_7628,RMVar_hsa_circ_245698,RMVar_hsa_circ_7588,RMVar_hsa_circ_310263,RMVar_hsa_circ_302790,RMVar_hsa_circ_40225,RMVar_hsa_circ_245696,RMVar_hsa_circ_122181,RMVar_hsa_circ_316225,RMVar_hsa_circ_336550,RMVar_hsa_circ_302188,RMVar_hsa_circ_245699,RMVar_hsa_circ_245697 30774 RMVar_ID_30774 Human_SNP_ID_326268973 A-to-I Human chr7 + 74389501 74389501 74389501 GAGTAGGGCCAGGCACAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGAGG GAGTAGGGCCAGGCACAGTGGCTCATGCCTGTGATCCCAGCACTTTGGGAGGCTGAGGCAGGAGG A G CLIP2 Ensembl:ENSG00000106665 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1554315419 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118036,RMVar_hsa_circ_83371,RMVar_hsa_circ_245670,RMVar_hsa_circ_80587,RMVar_hsa_circ_245682,RMVar_hsa_circ_245683,RMVar_hsa_circ_245698,RMVar_hsa_circ_7588,RMVar_hsa_circ_310263,RMVar_hsa_circ_245696,RMVar_hsa_circ_122181,RMVar_hsa_circ_316225,RMVar_hsa_circ_336550,RMVar_hsa_circ_297123,RMVar_hsa_circ_245697 30775 RMVar_ID_30775 Human_SNP_ID_326269074 A-to-I Human chr7 + 74389854 74389854 74389854 CCGAGAGGAGGAGGCTGCAGTGAGCTGAGATCATGCCACTGCACTCCAACCTGGGTGACCAGAGC CCGAGAGGAGGAGGCTGCAGTGAGCTGAGATCCTGCCACTGCACTCCAACCTGGGTGACCAGAGC A C CLIP2 Ensembl:ENSG00000106665 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1380905599 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118036,RMVar_hsa_circ_83371,RMVar_hsa_circ_245670,RMVar_hsa_circ_80587,RMVar_hsa_circ_245682,RMVar_hsa_circ_245683,RMVar_hsa_circ_245698,RMVar_hsa_circ_7588,RMVar_hsa_circ_310263,RMVar_hsa_circ_245696,RMVar_hsa_circ_122181,RMVar_hsa_circ_316225,RMVar_hsa_circ_336550,RMVar_hsa_circ_297123,RMVar_hsa_circ_245697 30776 RMVar_ID_30776 Human_SNP_ID_326270253 A-to-I Human chr7 + 74393588 74393588 74393588 GAACTCCCGACCTCAGGTGATCCACCCGCCTCAGCCTCCCAAAGTGCTGGGAATACAGGTGTGAG GAACTCCCGACCTCAGGTGATCCACCCGCCTCTGCCTCCCAAAGTGCTGGGAATACAGGTGTGAG A T CLIP2 Ensembl:ENSG00000106665 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1174529874 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118036,RMVar_hsa_circ_83371,RMVar_hsa_circ_245670,RMVar_hsa_circ_80587,RMVar_hsa_circ_245682,RMVar_hsa_circ_245683,RMVar_hsa_circ_245698,RMVar_hsa_circ_7588,RMVar_hsa_circ_310263,RMVar_hsa_circ_245696,RMVar_hsa_circ_122181,RMVar_hsa_circ_316225,RMVar_hsa_circ_336550,RMVar_hsa_circ_297123,RMVar_hsa_circ_245697 30777 RMVar_ID_30777 Human_SNP_ID_326270503 A-to-I Human chr7 + 74394350 74394350 74394350 TCTGCTCACCGCAACCTCTGCCTCCTGGGTTCAAGCAATTCTCCTGCCCCAGCTTCCCAAGTAGC TCTGCTCACCGCAACCTCTGCCTCCTGGGTTCCAGCAATTCTCCTGCCCCAGCTTCCCAAGTAGC A C CLIP2 Ensembl:ENSG00000106665 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1554316347 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118036,RMVar_hsa_circ_83371,RMVar_hsa_circ_245670,RMVar_hsa_circ_80587,RMVar_hsa_circ_245682,RMVar_hsa_circ_245683,RMVar_hsa_circ_245698,RMVar_hsa_circ_7588,RMVar_hsa_circ_310263,RMVar_hsa_circ_245696,RMVar_hsa_circ_122181,RMVar_hsa_circ_316225,RMVar_hsa_circ_336550,RMVar_hsa_circ_297123,RMVar_hsa_circ_245697 30778 RMVar_ID_30778 Human_SNP_ID_326270512 A-to-I Human chr7 + 74394376 74394376 74394376 GGGTTCAAGCAATTCTCCTGCCCCAGCTTCCCAAGTAGCTGGGATTACAGGCATGCGCCACCATG GGGTTCAAGCAATTCTCCTGCCCCAGCTTCCCGAGTAGCTGGGATTACAGGCATGCGCCACCATG A G CLIP2 Ensembl:ENSG00000106665 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1349007286 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118036,RMVar_hsa_circ_83371,RMVar_hsa_circ_245670,RMVar_hsa_circ_80587,RMVar_hsa_circ_245682,RMVar_hsa_circ_245683,RMVar_hsa_circ_245698,RMVar_hsa_circ_7588,RMVar_hsa_circ_310263,RMVar_hsa_circ_245696,RMVar_hsa_circ_122181,RMVar_hsa_circ_316225,RMVar_hsa_circ_336550,RMVar_hsa_circ_297123,RMVar_hsa_circ_245697 30779 RMVar_ID_30779 Human_SNP_ID_326271052 A-to-I Human chr7 + 74396576 74396576 74396576 ACAGCCTTGCTCTGTTGCCCAGGCTGGAGTGCAATGGCACGATCTTGGCTCACTGCAACCTCCAC ACAGCCTTGCTCTGTTGCCCAGGCTGGAGTGCCATGGCACGATCTTGGCTCACTGCAACCTCCAC A C CLIP2 Ensembl:ENSG00000106665 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1048999478 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118036,RMVar_hsa_circ_83371,RMVar_hsa_circ_245670,RMVar_hsa_circ_80587,RMVar_hsa_circ_245682,RMVar_hsa_circ_245683,RMVar_hsa_circ_245698,RMVar_hsa_circ_7588,RMVar_hsa_circ_310263,RMVar_hsa_circ_245696,RMVar_hsa_circ_122181,RMVar_hsa_circ_316225,RMVar_hsa_circ_336550,RMVar_hsa_circ_297123,RMVar_hsa_circ_245697 30780 RMVar_ID_30780 Human_SNP_ID_326271076 A-to-I Human chr7 + 74396686 74396686 74396686 GGGATTACAGGCACTTACCACCACGACTGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCA GGGATTACAGGCACTTACCACCACGACTGGCTGATTTTTGTATTTTTAGTAGAGATGGGGTTTCA A G CLIP2 Ensembl:ENSG00000106665 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1021919528 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118036,RMVar_hsa_circ_83371,RMVar_hsa_circ_245670,RMVar_hsa_circ_80587,RMVar_hsa_circ_245682,RMVar_hsa_circ_245683,RMVar_hsa_circ_245698,RMVar_hsa_circ_7588,RMVar_hsa_circ_310263,RMVar_hsa_circ_245696,RMVar_hsa_circ_122181,RMVar_hsa_circ_316225,RMVar_hsa_circ_336550,RMVar_hsa_circ_297123,RMVar_hsa_circ_245697 30781 RMVar_ID_30781 Human_SNP_ID_326287277 A-to-I Human chr7 + 74456412 74456412 74456412 CGACTCATAAATCCTGTAGTCTGGCCGGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGG CGACTCATAAATCCTGTAGTCTGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG A G GTF2IRD1 Ensembl:ENSG00000006704 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs911504151 Functional Loss SNV dbSNP153 33..33 33 - - - 30782 RMVar_ID_30782 Human_SNP_ID_326288015 A-to-I Human chr7 + 74459287 74459287 74459287 TTTGACTAGCCTGGCCAACACGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCCAGGCG TTTGACTAGCCTGGCCAACACGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCCAGGCG A G GTF2IRD1 Ensembl:ENSG00000006704 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs952573259 Functional Loss SNV dbSNP153 33..33 33 - - - 30783 RMVar_ID_30783 Human_SNP_ID_326288715 A-to-I Human chr7 + 74462164 74462164 74462164 AGGAGGCTGCGGCGGGAGGATCACTTGAGGCCAAGAATTTGAGACCAGCCTGGGCAACATAGCAA AGGAGGCTGCGGCGGGAGGATCACTTGAGGCCCAGAATTTGAGACCAGCCTGGGCAACATAGCAA A C GTF2IRD1 Ensembl:ENSG00000006704 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs926081734 Functional Loss SNV dbSNP153 33..33 33 - - - 30784 RMVar_ID_30784 Human_SNP_ID_326288732 A-to-I Human chr7 + 74462222 74462222 74462222 ATAGCAAGACCCCGTCTCTTAAAAAAAAAATTAGCCGGGTGTGGTGATGTGTGCCTGTAGCCCCA ATAGCAAGACCCCGTCTCTTAAAAAAAAAATTCGCCGGGTGTGGTGATGTGTGCCTGTAGCCCCA A C GTF2IRD1 Ensembl:ENSG00000006704 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1377220951 Functional Loss SNV dbSNP153 33..33 33 - - - 30785 RMVar_ID_30785 Human_SNP_ID_326289113 A-to-I Human chr7 + 74463801 74463801 74463801 GCTGGAGTGCAGTGGCGTGATCACGGCTCACTACAACCTCCGCCTCCCGGGTTCAGTTGATTCTC GCTGGAGTGCAGTGGCGTGATCACGGCTCACTTCAACCTCCGCCTCCCGGGTTCAGTTGATTCTC A T GTF2IRD1 Ensembl:ENSG00000006704 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1464882996 Functional Loss SNV dbSNP153 33..33 33 - - - 30786 RMVar_ID_30786 Human_SNP_ID_326289163 A-to-I Human chr7 + 74463998 74463998 74463998 CACCCATCTTGGCCTCCCAGAGTGCTGGAATTACAGGTGTGAGCCACCGCGCCCTGCCCTAGGAC CACCCATCTTGGCCTCCCAGAGTGCTGGAATTTCAGGTGTGAGCCACCGCGCCCTGCCCTAGGAC A T GTF2IRD1 Ensembl:ENSG00000006704 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs975383195 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16216135 30787 RMVar_ID_30787 Human_SNP_ID_326290965 A-to-I Human chr7 + 74471326 74471326 74471326 GGAAGACTGAGGCAGGAGGATCGCTTGAGGTCAGGAATCTGAGACCAGCTTAGACAGCCAAAAAA GGAAGACTGAGGCAGGAGGATCGCTTGAGGTCGGGAATCTGAGACCAGCTTAGACAGCCAAAAAA A G GTF2IRD1 Ensembl:ENSG00000006704 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1477861685 Functional Loss SNV dbSNP153 33..33 33 - - - 30788 RMVar_ID_30788 Human_SNP_ID_326291177 A-to-I Human chr7 + 74471827 74471827 74471827 CATCCTGGCCAATGTGGTGAAACTCTGTCTCTACTAAAATTACAAAAATTAGCCAGGCATGGTGG CATCCTGGCCAATGTGGTGAAACTCTGTCTCTGCTAAAATTACAAAAATTAGCCAGGCATGGTGG A G GTF2IRD1 Ensembl:ENSG00000006704 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1554332487 Functional Loss SNV dbSNP153 33..33 33 - - - 30789 RMVar_ID_30789 Human_SNP_ID_326294663 A-to-I Human chr7 + 74485851 74485851 74485851 GTGAGCCTGAGGCAGGAGAATTGCTTGAGTCCAGGAAGGTGGGGCTGCAGTGAGCTATGATCGTG GTGAGCCTGAGGCAGGAGAATTGCTTGAGTCCGGGAAGGTGGGGCTGCAGTGAGCTATGATCGTG A G GTF2IRD1 Ensembl:ENSG00000006704 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs372414617 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22483531 30790 RMVar_ID_30790 Human_SNP_ID_326298903 A-to-I Human chr7 + 74502128 74502128 74502128 ACCCGGCTAATTTCTGTATTTTTTGTAGAGACAGGATTTTGCCATGTTTCCCAGGCTGGTCTTGA ACCCGGCTAATTTCTGTATTTTTTGTAGAGACTGGATTTTGCCATGTTTCCCAGGCTGGTCTTGA A T GTF2IRD1 Ensembl:ENSG00000006704 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1481466799 Functional Loss SNV dbSNP153 33..33 33 - - - 30791 RMVar_ID_30791 Human_SNP_ID_326307027 A-to-I Human chr7 + 74533260 74533260 74533260 AGGTTCAAGCAATTCTCCTGCCTCCGCCTCCCAAGTAGCTGGGATTACAGGCATGCACCACCACA AGGTTCAAGCAATTCTCCTGCCTCCGCCTCCCGAGTAGCTGGGATTACAGGCATGCACCACCACA A G GTF2IRD1 Ensembl:ENSG00000006704 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1174347718 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10311,RMVar_hsa_circ_324396,RMVar_hsa_circ_370080,RMVar_hsa_circ_296453,RMVar_hsa_circ_29785,RMVar_hsa_circ_267507,RMVar_hsa_circ_13882,RMVar_hsa_circ_245704,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_245711 30792 RMVar_ID_30792 Human_SNP_ID_326307174 A-to-I Human chr7 + 74533846 74533846 74533846 ACTTGAGGTCAGGAGTTCAATGTGGACAACACAGTAAGACCCTGTCTCTACAAAAAAATTTAAAA ACTTGAGGTCAGGAGTTCAATGTGGACAACACGGTAAGACCCTGTCTCTACAAAAAAATTTAAAA A G GTF2IRD1 Ensembl:ENSG00000006704 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1554349542 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2157298,Human_miRNA_ID_2157299 RMVar_hsa_circ_10311,RMVar_hsa_circ_324396,RMVar_hsa_circ_370080,RMVar_hsa_circ_296453,RMVar_hsa_circ_29785,RMVar_hsa_circ_267507,RMVar_hsa_circ_13882,RMVar_hsa_circ_245704,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_245711 30793 RMVar_ID_30793 Human_SNP_ID_326307209 A-to-I Human chr7 + 74534016 74534016 74534016 GCACCACTGCACTCCAGCCTGGGTGATAGAGCAAGACCCCAACTCAAAAAAAAAAAAAAGGATCC GCACCACTGCACTCCAGCCTGGGTGATAGAGCCAGACCCCAACTCAAAAAAAAAAAAAAGGATCC A C GTF2IRD1 Ensembl:ENSG00000006704 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1166466426 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10311,RMVar_hsa_circ_324396,RMVar_hsa_circ_370080,RMVar_hsa_circ_296453,RMVar_hsa_circ_29785,RMVar_hsa_circ_267507,RMVar_hsa_circ_13882,RMVar_hsa_circ_245704,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_245711 30794 RMVar_ID_30794 Human_SNP_ID_326307348 A-to-I Human chr7 + 74534620 74534620 74534620 ATGGGAGGCAGAGCTGGGGGAGCGAGGCTGACAATGACTCCTGTTTTCACGCTGAGAGACCCCAC ATGGGAGGCAGAGCTGGGGGAGCGAGGCTGACGATGACTCCTGTTTTCACGCTGAGAGACCCCAC A G GTF2IRD1 Ensembl:ENSG00000006704 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs73135381 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_3421,GWAS_ID_3422,GWAS_ID_3423,GWAS_ID_3424,GWAS_ID_3425,GWAS_ID_3426,GWAS_ID_3427,GWAS_ID_3428,GWAS_ID_3429,GWAS_ID_3430,GWAS_ID_3431,GWAS_ID_3432,GWAS_ID_3433,GWAS_ID_3434,GWAS_ID_3435,GWAS_ID_3436 RMVar_hsa_circ_10311,RMVar_hsa_circ_324396,RMVar_hsa_circ_370080,RMVar_hsa_circ_296453,RMVar_hsa_circ_29785,RMVar_hsa_circ_267507,RMVar_hsa_circ_13882,RMVar_hsa_circ_245704,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_245711 30795 RMVar_ID_30795 Human_SNP_ID_326307349 A-to-I Human chr7 + 74534620 74534620 74534620 ATGGGAGGCAGAGCTGGGGGAGCGAGGCTGACAATGACTCCTGTTTTCACGCTGAGAGACCCCAC ATGGGAGGCAGAGCTGGGGGAGCGAGGCTGACTATGACTCCTGTTTTCACGCTGAGAGACCCCAC A T GTF2IRD1 Ensembl:ENSG00000006704 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs73135381 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_3421,GWAS_ID_3422,GWAS_ID_3423,GWAS_ID_3424,GWAS_ID_3425,GWAS_ID_3426,GWAS_ID_3427,GWAS_ID_3428,GWAS_ID_3429,GWAS_ID_3430,GWAS_ID_3431,GWAS_ID_3432,GWAS_ID_3433,GWAS_ID_3434,GWAS_ID_3435,GWAS_ID_3436 RMVar_hsa_circ_10311,RMVar_hsa_circ_324396,RMVar_hsa_circ_370080,RMVar_hsa_circ_296453,RMVar_hsa_circ_29785,RMVar_hsa_circ_267507,RMVar_hsa_circ_13882,RMVar_hsa_circ_245704,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_245711 30796 RMVar_ID_30796 Human_SNP_ID_326313010 A-to-I Human chr7 + 74558002 74558002 74558002 CACACAGAATTTAATAGACAAGGGCCCGGCACAGTGGCTCCTGCCTGTAATCCCAGCACTTTTGG CACACAGAATTTAATAGACAAGGGCCCGGCACGGTGGCTCCTGCCTGTAATCCCAGCACTTTTGG A G GTF2IRD1 Ensembl:ENSG00000006704 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1476512339 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17949,RMVar_hsa_circ_10311,RMVar_hsa_circ_296453,RMVar_hsa_circ_29785,RMVar_hsa_circ_13882,RMVar_hsa_circ_245705,RMVar_hsa_circ_13887,RMVar_hsa_circ_107114,RMVar_hsa_circ_245711,RMVar_hsa_circ_21232 30797 RMVar_ID_30797 Human_SNP_ID_326321517 A-to-I Human chr7 + 74592385 74592385 74592385 CCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGTCACCACACCCAGCCCCCCCTTTTTTTT CCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGTCACCACACCCAGCCCCCCCTTTTTTTT A G GTF2IRD1 Ensembl:ENSG00000006704 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1281338925 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10311,RMVar_hsa_circ_29785,RMVar_hsa_circ_21232,RMVar_hsa_circ_343619,RMVar_hsa_circ_347068,RMVar_hsa_circ_8441 30798 RMVar_ID_30798 Human_SNP_ID_326322294 A-to-I Human chr7 + 74595338 74595338 74595338 TGAGGCAGGAGAATTGCGTGAACCCGGGAGGCAGAGGTTGCGGTGAACTGAGATCGCGCCCCTGC TGAGGCAGGAGAATTGCGTGAACCCGGGAGGCGGAGGTTGCGGTGAACTGAGATCGCGCCCCTGC A G GTF2IRD1 Ensembl:ENSG00000006704 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1554371904 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10311,RMVar_hsa_circ_347068 30799 RMVar_ID_30799 Human_SNP_ID_326322829 A-to-I Human chr7 + 74597581 74597581 74597581 GTTGGCCGGGCTGGTCTCAAACACCTGACCTCAAGTGATCTTCCCACCCCAGCATCCCAAAGTGC GTTGGCCGGGCTGGTCTCAAACACCTGACCTCGAGTGATCTTCCCACCCCAGCATCCCAAAGTGC A G GTF2IRD1 Ensembl:ENSG00000006704 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1263714751 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10311,RMVar_hsa_circ_347068 30800 RMVar_ID_30800 Human_SNP_ID_326322835 A-to-I Human chr7 + 74597594 74597594 74597594 GTCTCAAACACCTGACCTCAAGTGATCTTCCCACCCCAGCATCCCAAAGTGCTGGGATTACAGGC GTCTCAAACACCTGACCTCAAGTGATCTTCCCGCCCCAGCATCCCAAAGTGCTGGGATTACAGGC A G GTF2IRD1 Ensembl:ENSG00000006704 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1554372752 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10311,RMVar_hsa_circ_347068 30801 RMVar_ID_30801 Human_SNP_ID_326322839 A-to-I Human chr7 + 74597599 74597599 74597599 AAACACCTGACCTCAAGTGATCTTCCCACCCCAGCATCCCAAAGTGCTGGGATTACAGGCGTGAG AAACACCTGACCTCAAGTGATCTTCCCACCCCGGCATCCCAAAGTGCTGGGATTACAGGCGTGAG A G GTF2IRD1 Ensembl:ENSG00000006704 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1554372753 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10311,RMVar_hsa_circ_347068 30802 RMVar_ID_30802 Human_SNP_ID_326323278 A-to-I Human chr7 + 74599732 74599732 74599732 GAGACAGGGTTTCAACCTTCACCATGTTGCCCAGGCTGGTCTCGAACTCCTGACCTCAGTCAATC GAGACAGGGTTTCAACCTTCACCATGTTGCCCGGGCTGGTCTCGAACTCCTGACCTCAGTCAATC A G GTF2IRD1 Ensembl:ENSG00000006704 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1479693178 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10311,RMVar_hsa_circ_347068 30803 RMVar_ID_30803 Human_SNP_ID_326339729 A-to-I Human chr7 + 74661523 74661523 74661523 CGACATGGCGAAACCCCGTCTGTACTAAAAATACAAAAATTAGCCGGGTGTGGTGGCGTGCGTAC CGACATGGCGAAACCCCGTCTGTACTAAAAATGCAAAAATTAGCCGGGTGTGGTGGCGTGCGTAC A G GTF2I Ensembl:ENSG00000263001 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1460210211 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16216812 30804 RMVar_ID_30804 Human_SNP_ID_326340131 A-to-I Human chr7 + 74662704 74662704 74662704 ACCACCACGCCTGGCTAATTTTTTGTATTTTTAGTAGACACGGGGTTTCATCATGCTGGCCAGGC ACCACCACGCCTGGCTAATTTTTTGTATTTTTGGTAGACACGGGGTTTCATCATGCTGGCCAGGC A G GTF2I Ensembl:ENSG00000263001 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1554387121 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3099866,Human_RBP_ID_16216850 30805 RMVar_ID_30805 Human_SNP_ID_326341270 A-to-I Human chr7 + 74667178 74667178 74667178 AGGAAAACAAACAAACAAAAAAACACATCTCTACTGAAAATACAGAAGTTAGCTGGGAGTGGTGA AGGAAAACAAACAAACAAAAAAACACATCTCTGCTGAAAATACAGAAGTTAGCTGGGAGTGGTGA A G GTF2I Ensembl:ENSG00000263001 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs185895209 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9212985 30806 RMVar_ID_30806 Human_SNP_ID_326341977 A-to-I Human chr7 + 74669735 74669735 74669735 TTGTATTATTAGTAGAGACGGGGTTTCACCATATTGGCCAGGCTGGTCTCAAATTCCTGACTTTG TTGTATTATTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGGTCTCAAATTCCTGACTTTG A G GTF2I Ensembl:ENSG00000263001 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1299210480 Functional Loss SNV dbSNP153 33..33 33 - - - 30807 RMVar_ID_30807 Human_SNP_ID_326342349 A-to-I Human chr7 + 74671213 74671213 74671213 GGTTCAAGTGATTCTCTTGCCTCAGCCTCCCGAGTAGCTGAGATTACAGGCGTGCACCACCACAC GGTTCAAGTGATTCTCTTGCCTCAGCCTCCCGGGTAGCTGAGATTACAGGCGTGCACCACCACAC A G GTF2I Ensembl:ENSG00000263001 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1358432101 Functional Loss SNV dbSNP153 33..33 33 - - - 30808 RMVar_ID_30808 Human_SNP_ID_326342352 A-to-I Human chr7 + 74671226 74671226 74671226 CTCTTGCCTCAGCCTCCCGAGTAGCTGAGATTACAGGCGTGCACCACCACACCCGGCTAATTTTT CTCTTGCCTCAGCCTCCCGAGTAGCTGAGATTGCAGGCGTGCACCACCACACCCGGCTAATTTTT A G GTF2I Ensembl:ENSG00000263001 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1028225994 Functional Loss SNV dbSNP153 33..33 33 - - - 30809 RMVar_ID_30809 Human_SNP_ID_326342370 A-to-I Human chr7 + 74671276 74671276 74671276 ACCCGGCTAATTTTTGTATTTTTGGTAGAGACAGAATTTCACCATGATGTCCAGGCTGGTCTTGA ACCCGGCTAATTTTTGTATTTTTGGTAGAGACGGAATTTCACCATGATGTCCAGGCTGGTCTTGA A G GTF2I Ensembl:ENSG00000263001 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs782264673 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16217064 30810 RMVar_ID_30810 Human_SNP_ID_326342374 A-to-I Human chr7 + 74671287 74671287 74671287 TTTTGTATTTTTGGTAGAGACAGAATTTCACCATGATGTCCAGGCTGGTCTTGAACTCCTGACCT TTTTGTATTTTTGGTAGAGACAGAATTTCACCGTGATGTCCAGGCTGGTCTTGAACTCCTGACCT A G GTF2I Ensembl:ENSG00000263001 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1015302196 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16217066 30811 RMVar_ID_30811 Human_SNP_ID_326342527 A-to-I Human chr7 + 74671873 74671873 74671873 GGGTGTGGTGGTGCATTCCTGTAGTCTCAGCTACTAAGAAGGATGAGGTGGGAGGATTGCTTGAG GGGTGTGGTGGTGCATTCCTGTAGTCTCAGCTGCTAAGAAGGATGAGGTGGGAGGATTGCTTGAG A G GTF2I Ensembl:ENSG00000263001 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1288542692 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7757589,Human_RBP_ID_16217074 30812 RMVar_ID_30812 Human_SNP_ID_326342663 A-to-I Human chr7 + 74672472 74672471 74672473 TGAGGCAGCAGAATCACTTGGACCCGGAAAGCAGAGTTTCCAGTGAGCCAGGATCGTGCCACTGT TGAGGCAGCAGAATCACTTGGACCCGGAAAGC__AGTTTCCAGTGAGCCAGGATCGTGCCACTGT CAG C GTF2I Ensembl:ENSG00000263001 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs373468560 Functional Loss DEL dbSNP153 33..34 33 - - - 30813 RMVar_ID_30813 Human_SNP_ID_326342864 A-to-I Human chr7 + 74673350 74673350 74673350 AGGCAGCCAGACAACTCCTGCTCTTAACTGCTATGTGGTTTTTGGATTTGTTTGTTTGTTTGTTT AGGCAGCCAGACAACTCCTGCTCTTAACTGCTGTGTGGTTTTTGGATTTGTTTGTTTGTTTGTTT A G GTF2I Ensembl:ENSG00000263001 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1264342559 Functional Loss SNV dbSNP153 33..33 33 - - - 30814 RMVar_ID_30814 Human_SNP_ID_326342880 A-to-I Human chr7 + 74673425 74673425 74673425 TGAGATGGAGTTTCTCTCTTGTTGCCCAGGCTAGAGTGCAATGGTGTGATCTGACCTCAGCTCAC TGAGATGGAGTTTCTCTCTTGTTGCCCAGGCTGGAGTGCAATGGTGTGATCTGACCTCAGCTCAC A G GTF2I Ensembl:ENSG00000263001 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1176856880 Functional Loss SNV dbSNP153 33..33 33 - - - 30815 RMVar_ID_30815 Human_SNP_ID_326343115 A-to-I Human chr7 + 74674269 74674269 74674269 TTAAATTTTTGGTAGAGAAGGGATCTCACTCTATTGCCAAGCTGGTGTCGAACTCTTGGTCTTAA TTAAATTTTTGGTAGAGAAGGGATCTCACTCTGTTGCCAAGCTGGTGTCGAACTCTTGGTCTTAA A G GTF2I Ensembl:ENSG00000263001 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs959935490 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16217120 RMVar_hsa_circ_245716 30816 RMVar_ID_30816 Human_SNP_ID_326343116 A-to-I Human chr7 + 74674269 74674269 74674269 TTAAATTTTTGGTAGAGAAGGGATCTCACTCTATTGCCAAGCTGGTGTCGAACTCTTGGTCTTAA TTAAATTTTTGGTAGAGAAGGGATCTCACTCTTTTGCCAAGCTGGTGTCGAACTCTTGGTCTTAA A T GTF2I Ensembl:ENSG00000263001 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs959935490 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16217120 RMVar_hsa_circ_245716 30817 RMVar_ID_30817 Human_SNP_ID_326343118 A-to-I Human chr7 + 74674275 74674275 74674275 TTTTGGTAGAGAAGGGATCTCACTCTATTGCCAAGCTGGTGTCGAACTCTTGGTCTTAAGCAGCC TTTTGGTAGAGAAGGGATCTCACTCTATTGCCCAGCTGGTGTCGAACTCTTGGTCTTAAGCAGCC A C GTF2I Ensembl:ENSG00000263001 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,cerebellum - 29129909,30559470 RNA-Seq:(High) rs587762247 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16217120 RMVar_hsa_circ_245716 30818 RMVar_ID_30818 Human_SNP_ID_326343905 A-to-I Human chr7 + 74677635 74677635 74677635 GAAACCCCATCTCTACTAAAAAAAAGAAAATTAGCCGGGCGTGGTGACATACACCTGTAATCCTA GAAACCCCATCTCTACTAAAAAAAAGAAAATTTGCCGGGCGTGGTGACATACACCTGTAATCCTA A T GTF2I Ensembl:ENSG00000263001 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1554392768 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7757597 30819 RMVar_ID_30819 Human_SNP_ID_326343928 A-to-I Human chr7 + 74677707 74677707 74677707 GGGAGGCTGAGGCAGGAGAATTGCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCCAAGATCACG GGGAGGCTGAGGCAGGAGAATTGCTTGAACCCGGGAGGCGGAGGTTGCAGTGAGCCAAGATCACG A G GTF2I Ensembl:ENSG00000263001 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs912145057 Functional Loss SNV dbSNP153 33..33 33 - - - 30820 RMVar_ID_30820 Human_SNP_ID_326343938 A-to-I Human chr7 + 74677731 74677731 74677731 TTGAACCCAGGAGGCGGAGGTTGCAGTGAGCCAAGATCACGCCACTGCACTCCAGCCTGGGCGAC TTGAACCCAGGAGGCGGAGGTTGCAGTGAGCCGAGATCACGCCACTGCACTCCAGCCTGGGCGAC A G GTF2I Ensembl:ENSG00000263001 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1048145011 Functional Loss SNV dbSNP153 33..33 33 - - - 30821 RMVar_ID_30821 Human_SNP_ID_326343940 A-to-I Human chr7 + 74677737 74677737 74677737 CCAGGAGGCGGAGGTTGCAGTGAGCCAAGATCACGCCACTGCACTCCAGCCTGGGCGACAGAGTG CCAGGAGGCGGAGGTTGCAGTGAGCCAAGATCGCGCCACTGCACTCCAGCCTGGGCGACAGAGTG A G GTF2I Ensembl:ENSG00000263001 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1003863182 Functional Loss SNV dbSNP153 33..33 33 - - - 30822 RMVar_ID_30822 Human_SNP_ID_326378158 A-to-I Human chr7 - 74848673 74848673 74848673 TACCACCACGCCCGGCTAATTTTTACGTTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGC TACCACCACGCCCGGCTAATTTTTACGTTTTTGGTAGAGACGGGGTTTCACCATGTTGGCCAGGC T C GTF2IRD2,STAG3L2 Ensembl:ENSG00000196275,Ensembl:ENSG00000277072 Protein coding,Pseudogene intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1458352354 Functional Loss SNV dbSNP153 33..33 33 - - - 30823 RMVar_ID_30823 Human_SNP_ID_326382741 A-to-I Human chr7 - 74872020 74872020 74872020 TGCCTCCCAGGTTCAAGTGATTCTTCTGCCTCAGCCTCTGAGGTAGCTGGGATTACAGGTACCAG TGCCTCCCAGGTTCAAGTGATTCTTCTGCCTCGGCCTCTGAGGTAGCTGGGATTACAGGTACCAG T C STAG3L2 Ensembl:ENSG00000277072 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404470140 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18520221 30824 RMVar_ID_30824 Human_SNP_ID_326384299 A-to-I Human chr7 - 74876953 74876953 74876953 GAATTGCTTGAACCCGGGATTGCAGTGAGCCAAGATCGCACCACTACACTTCAGCCTGGGTGACA GAATTGCTTGAACCCGGGATTGCAGTGAGCCAGGATCGCACCACTACACTTCAGCCTGGGTGACA T C STAG3L2 Ensembl:ENSG00000277072 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1416782022 Functional Loss SNV dbSNP153 33..33 33 - - - 30825 RMVar_ID_30825 Human_SNP_ID_326384963 A-to-I Human chr7 - 74879759 74879759 74879759 CCTCGGGTGATCCACCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGTGCC CCTCGGGTGATCCACCCACCTCAGCCTCCCAAGGTGCTGGGATTACAGGTGTGAGCCACCGTGCC T C STAG3L2 Ensembl:ENSG00000277072 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1554426072 Functional Loss SNV dbSNP153 33..33 33 - - - 30826 RMVar_ID_30826 Human_SNP_ID_326385148 A-to-I Human chr7 - 74880259 74880259 74880259 GCCTCAAACTCCTGGCCTTAAGCAATCCTCCTACTTCAGCCTCCCAAAGTGCTGAGATTATAGGT GCCTCAAACTCCTGGCCTTAAGCAATCCTCCTCCTTCAGCCTCCCAAAGTGCTGAGATTATAGGT T G STAG3L2 Ensembl:ENSG00000277072 Pseudogene intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1334214388 Functional Loss SNV dbSNP153 33..33 33 - - - 30827 RMVar_ID_30827 Human_SNP_ID_326385160 A-to-I Human chr7 - 74880318 74880318 74880318 ACGAGGTCTTGCTTTGTTTTCCAGGCTGGAGTACAGTGGCTCAATCATAGCTCACTGCAGCCTCA ACGAGGTCTTGCTTTGTTTTCCAGGCTGGAGTCCAGTGGCTCAATCATAGCTCACTGCAGCCTCA T G STAG3L2 Ensembl:ENSG00000277072 Pseudogene intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1438584733 Functional Loss SNV dbSNP153 33..33 33 - - - 30828 RMVar_ID_30828 Human_SNP_ID_326385170 A-to-I Human chr7 - 74880354 74880354 74880354 GGGAGCCACTGTCCCGGCATATTATTACTTTTAGAGACGAGGTCTTGCTTTGTTTTCCAGGCTGG GGGAGCCACTGTCCCGGCATATTATTACTTTTGGAGACGAGGTCTTGCTTTGTTTTCCAGGCTGG T C STAG3L2 Ensembl:ENSG00000277072 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223144931 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1052894,Human_RBP_ID_1222322,Human_RBP_ID_7757818,Human_RBP_ID_8273024,Human_RBP_ID_17428095,Human_RBP_ID_18103998,Human_RBP_ID_18520143,Human_RBP_ID_18540580,Human_RBP_ID_27770207 30829 RMVar_ID_30829 Human_SNP_ID_326385195 A-to-I Human chr7 - 74880415 74880415 74880415 CCAGGCTGGTCTCGAAAGCCTGACCTCAAGTGATCCGCCCACCTTAGCCTCCCAAAGTGTGGGGA CCAGGCTGGTCTCGAAAGCCTGACCTCAAGTGGTCCGCCCACCTTAGCCTCCCAAAGTGTGGGGA T C STAG3L2 Ensembl:ENSG00000277072 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1199959935 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18520223,Human_RBP_ID_23198534,Human_RBP_ID_26117054 30830 RMVar_ID_30830 Human_SNP_ID_326385216 A-to-I Human chr7 - 74880505 74880505 74880505 CTCCTCCCAGGTAGCTGGGGTTACAGGTGTGCAGCACCACACCTGGCTAATTTTTTTATTTTTAG CTCCTCCCAGGTAGCTGGGGTTACAGGTGTGCGGCACCACACCTGGCTAATTTTTTTATTTTTAG T C STAG3L2 Ensembl:ENSG00000277072 Pseudogene intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1554426165 Functional Loss SNV dbSNP153 33..33 33 - - - 30831 RMVar_ID_30831 Human_SNP_ID_326385243 A-to-I Human chr7 - 74880571 74880571 74880571 TGGAGTGCAATGAGGCGATCTCACCTCATGCAACCTCCATCTCCCGGGTTCAAGCGATTCTCCTG TGGAGTGCAATGAGGCGATCTCACCTCATGCAGCCTCCATCTCCCGGGTTCAAGCGATTCTCCTG T C STAG3L2 Ensembl:ENSG00000277072 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs587608832 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8273025 30832 RMVar_ID_30832 Human_SNP_ID_326387476 A-to-I Human chr7 - 74889590 74889575 74889591 GACCGAAGCGGGAGGATTGCTTGGGAGACCGAAGCGGGAGGATTGCTTGAGCCCGGAGAGTTTGA GACCGAAGCGGGAGGATTGCTTGGGAGACCG________________TGAGCCCGGAGAGTTTGA AAGCAATCCTCCCGCTT A STAG3L2 Ensembl:ENSG00000277072 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1554427162 Functional Loss DEL dbSNP153 32..47 33 - - - Human_RBP_ID_16218499 30833 RMVar_ID_30833 Human_SNP_ID_326391102 A-to-I Human chr7 - 74906144 74906144 74906144 GCTTCTGGACTCGTGGTTCGTGATGTTGTCACATTAGAAACAGATCTAGCACGGTTACAAGTTTA GCTTCTGGACTCGTGGTTCGTGATGTTGTCACGTTAGAAACAGATCTAGCACGGTTACAAGTTTA T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs587678468 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_3437,GWAS_ID_3438,GWAS_ID_3439 30834 RMVar_ID_30834 Human_SNP_ID_326391103 A-to-I Human chr7 - 74906144 74906144 74906144 GCTTCTGGACTCGTGGTTCGTGATGTTGTCACATTAGAAACAGATCTAGCACGGTTACAAGTTTA GCTTCTGGACTCGTGGTTCGTGATGTTGTCACCTTAGAAACAGATCTAGCACGGTTACAAGTTTA T G - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs587678468 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_3437,GWAS_ID_3438,GWAS_ID_3439 30835 RMVar_ID_30835 Human_SNP_ID_326392386 A-to-I Human chr7 + 74910676 74910676 74910676 GAGACACTGCCCTTCAGCCTGGGCAACAGAGCAAGACTGTGTCTCACAAAACAAAAACAAAAACA GAGACACTGCCCTTCAGCCTGGGCAACAGAGCGAGACTGTGTCTCACAAAACAAAAACAAAAACA A G NONHSAG047974.2,RF00017-4525 RNACentral:URS00009BC4B5,RNACentral:URS00009368C0 lincRNA,SRP RNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs587673164 Functional Loss SNV dbSNP153 33..33 33 - - - 30836 RMVar_ID_30836 Human_SNP_ID_326395311 A-to-I Human chr7 + 74925419 74925419 74925419 GCCAGGCTGGTCTCGAACTCCAGGCCTCATGTAATCCGCCCACCTTGGCCTTTCACTTAGCATAA GCCAGGCTGGTCTCGAACTCCAGGCCTCATGTCATCCGCCCACCTTGGCCTTTCACTTAGCATAA A C lnc-CASTOR2-3,lnc-CASTOR2-2,NONHSAG047976.2,RF00017-4525 RNACentral:URS00008B2AD9,RNACentral:URS00009B7DBE,RNACentral:URS00009C2189,RNACentral:URS00009368C0 lincRNA,lincRNA,lincRNA,SRP RNA intron,exon,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1387148657 Functional Loss SNV dbSNP153 33..33 33 - - - 30837 RMVar_ID_30837 Human_SNP_ID_326408998 A-to-I Human chr7 + 74993580 74993580 74993580 TCAAGTGATTCTCCTGCTTCAGCCTCTGGAGTAGCTGAGATTACAGGCACCTGCTACCACACCCA TCAAGTGATTCTCCTGCTTCAGCCTCTGGAGTGGCTGAGATTACAGGCACCTGCTACCACACCCA A G CASTOR2 Ensembl:ENSG00000274070 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1251895041 Functional Loss SNV dbSNP153 33..33 33 - - - 30838 RMVar_ID_30838 Human_SNP_ID_8138989 A-to-I Human chr1 - 30873218 30873218 30873218 ATACCAGAAGCCTGACAAGCAGGAGGAGTTCTATGCCTAGTGGAGCCACAGTGCCTCCCTGCAGC ATACCAGAAGCCTGACAAGCAGGAGGAGTTCTGTGCCTAGTGGAGCCACAGTGCCTCCCTGCAGC T C SDC3 Ensembl:ENSG00000162512 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1425165949 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113905,RMVar_hsa_circ_130979 30839 RMVar_ID_30839 Human_SNP_ID_8156316 A-to-I Human chr1 - 30938393 30938393 30938393 CAAAAATTAGCTGGGCGTGGTGGCACACGCCTATAGTCCCAGCTACTTGGGAGGCTGAGTCAGGA CAAAAATTAGCTGGGCGTGGTGGCACACGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGTCAGGA T C PUM1 Ensembl:ENSG00000134644 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1262999158 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15392,RMVar_hsa_circ_130982,RMVar_hsa_circ_78087,RMVar_hsa_circ_121030,RMVar_hsa_circ_130983,RMVar_hsa_circ_124647,RMVar_hsa_circ_297892,RMVar_hsa_circ_371999,RMVar_hsa_circ_378319,RMVar_hsa_circ_348445,RMVar_hsa_circ_278509,RMVar_hsa_circ_36810,RMVar_hsa_circ_130984,RMVar_hsa_circ_130985,RMVar_hsa_circ_130986 30840 RMVar_ID_30840 Human_SNP_ID_8156349 A-to-I Human chr1 - 30938539 30938539 30938539 TTTAAAAAGAAAAAATAGGGGCTGGAGACGGTAGCTCATACCTGTAATCCCAACACTTTGGGAGG TTTAAAAAGAAAAAATAGGGGCTGGAGACGGTGGCTCATACCTGTAATCCCAACACTTTGGGAGG T C PUM1 Ensembl:ENSG00000134644 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs960837320 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15392,RMVar_hsa_circ_130982,RMVar_hsa_circ_78087,RMVar_hsa_circ_121030,RMVar_hsa_circ_130983,RMVar_hsa_circ_124647,RMVar_hsa_circ_297892,RMVar_hsa_circ_371999,RMVar_hsa_circ_378319,RMVar_hsa_circ_348445,RMVar_hsa_circ_278509,RMVar_hsa_circ_36810,RMVar_hsa_circ_130984,RMVar_hsa_circ_130985,RMVar_hsa_circ_130986 30841 RMVar_ID_30841 Human_SNP_ID_8156377 A-to-I Human chr1 - 30938675 30938675 30938675 TATTTTTAGTAGAGACAGGGTTTCACCATGTTAGCCAGGATGGTCTCGATCTCCTGACCTCATGA TATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGATGGTCTCGATCTCCTGACCTCATGA T C PUM1 Ensembl:ENSG00000134644 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs539801883 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15392,RMVar_hsa_circ_130982,RMVar_hsa_circ_78087,RMVar_hsa_circ_121030,RMVar_hsa_circ_130983,RMVar_hsa_circ_124647,RMVar_hsa_circ_297892,RMVar_hsa_circ_371999,RMVar_hsa_circ_378319,RMVar_hsa_circ_348445,RMVar_hsa_circ_278509,RMVar_hsa_circ_36810,RMVar_hsa_circ_130984,RMVar_hsa_circ_130985,RMVar_hsa_circ_130986 30842 RMVar_ID_30842 Human_SNP_ID_8157597 A-to-I Human chr1 - 30942955 30942955 30942955 GGCTAGGAGTACAGGAACAGCCTGGGCAACATAGCGAATCTCCGTCTCTACACACAATTTTTTTT GGCTAGGAGTACAGGAACAGCCTGGGCAACATGGCGAATCTCCGTCTCTACACACAATTTTTTTT T C PUM1 Ensembl:ENSG00000134644 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs938248555 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9513440 RMVar_hsa_circ_130982,RMVar_hsa_circ_78087,RMVar_hsa_circ_121030,RMVar_hsa_circ_130983,RMVar_hsa_circ_124647,RMVar_hsa_circ_371999,RMVar_hsa_circ_378319,RMVar_hsa_circ_348445,RMVar_hsa_circ_278509,RMVar_hsa_circ_36810,RMVar_hsa_circ_83915,RMVar_hsa_circ_311107,RMVar_hsa_circ_130984,RMVar_hsa_circ_130985,RMVar_hsa_circ_130986,RMVar_hsa_circ_315757,RMVar_hsa_circ_327662,RMVar_hsa_circ_372758,RMVar_hsa_circ_320131,RMVar_hsa_circ_312856,RMVar_hsa_circ_298189,RMVar_hsa_circ_306228,RMVar_hsa_circ_130987,RMVar_hsa_circ_130989,RMVar_hsa_circ_130990,RMVar_hsa_circ_130988,RMVar_hsa_circ_109101,RMVar_hsa_circ_116545,RMVar_hsa_circ_86432,RMVar_hsa_circ_130993,RMVar_hsa_circ_78850,RMVar_hsa_circ_78901,RMVar_hsa_circ_130995,RMVar_hsa_circ_130996,RMVar_hsa_circ_130997,RMVar_hsa_circ_130994,RMVar_hsa_circ_130992 30843 RMVar_ID_30843 Human_SNP_ID_8158287 A-to-I Human chr1 - 30945981 30945981 30945981 CAGGAGTTCGAGACAGCCTGGCCAACATGGCAAGACCCCGTCTCTAGTAAAAATACAAAAATTAG CAGGAGTTCGAGACAGCCTGGCCAACATGGCAGGACCCCGTCTCTAGTAAAAATACAAAAATTAG T C PUM1 Ensembl:ENSG00000134644 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs895958462 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121030,RMVar_hsa_circ_130983,RMVar_hsa_circ_124647,RMVar_hsa_circ_371999,RMVar_hsa_circ_348445,RMVar_hsa_circ_278509,RMVar_hsa_circ_36810,RMVar_hsa_circ_83915,RMVar_hsa_circ_130984,RMVar_hsa_circ_130985,RMVar_hsa_circ_130986,RMVar_hsa_circ_315757,RMVar_hsa_circ_327662,RMVar_hsa_circ_372758,RMVar_hsa_circ_320131,RMVar_hsa_circ_312856,RMVar_hsa_circ_298189,RMVar_hsa_circ_306228,RMVar_hsa_circ_130987,RMVar_hsa_circ_130989,RMVar_hsa_circ_130990,RMVar_hsa_circ_130988,RMVar_hsa_circ_109101,RMVar_hsa_circ_116545,RMVar_hsa_circ_86432,RMVar_hsa_circ_130993,RMVar_hsa_circ_78901,RMVar_hsa_circ_130995,RMVar_hsa_circ_130996,RMVar_hsa_circ_130997,RMVar_hsa_circ_130994,RMVar_hsa_circ_86246,RMVar_hsa_circ_338078,RMVar_hsa_circ_372401,RMVar_hsa_circ_346873,RMVar_hsa_circ_274987,RMVar_hsa_circ_67706,RMVar_hsa_circ_130999,RMVar_hsa_circ_25419,RMVar_hsa_circ_31601,RMVar_hsa_circ_131000,RMVar_hsa_circ_131001,RMVar_hsa_circ_130998 30844 RMVar_ID_30844 Human_SNP_ID_8158458 A-to-I Human chr1 - 30946631 30946630 30946632 ATATAAAATAATTTTTTTTTTTTTTTTGAGACAGAGTCTCGCTCTGTCGCTCAGGCTGGAGTGCA ATATAAAATAATTTTTTTTTTTTTTTTGAGA__GAGTCTCGCTCTGTCGCTCAGGCTGGAGTGCA CTG C PUM1 Ensembl:ENSG00000134644 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031267430 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_121030,RMVar_hsa_circ_130983,RMVar_hsa_circ_124647,RMVar_hsa_circ_371999,RMVar_hsa_circ_348445,RMVar_hsa_circ_278509,RMVar_hsa_circ_36810,RMVar_hsa_circ_83915,RMVar_hsa_circ_130984,RMVar_hsa_circ_130985,RMVar_hsa_circ_130986,RMVar_hsa_circ_315757,RMVar_hsa_circ_327662,RMVar_hsa_circ_372758,RMVar_hsa_circ_320131,RMVar_hsa_circ_312856,RMVar_hsa_circ_298189,RMVar_hsa_circ_306228,RMVar_hsa_circ_130987,RMVar_hsa_circ_130989,RMVar_hsa_circ_130990,RMVar_hsa_circ_130988,RMVar_hsa_circ_109101,RMVar_hsa_circ_116545,RMVar_hsa_circ_86432,RMVar_hsa_circ_130993,RMVar_hsa_circ_78901,RMVar_hsa_circ_130995,RMVar_hsa_circ_130996,RMVar_hsa_circ_130997,RMVar_hsa_circ_130994,RMVar_hsa_circ_86246,RMVar_hsa_circ_338078,RMVar_hsa_circ_372401,RMVar_hsa_circ_346873,RMVar_hsa_circ_274987,RMVar_hsa_circ_67706,RMVar_hsa_circ_130999,RMVar_hsa_circ_25419,RMVar_hsa_circ_31601,RMVar_hsa_circ_131000,RMVar_hsa_circ_131001,RMVar_hsa_circ_130998 30845 RMVar_ID_30845 Human_SNP_ID_8158459 A-to-I Human chr1 - 30946631 30946631 30946631 ATATAAAATAATTTTTTTTTTTTTTTTGAGACAGAGTCTCGCTCTGTCGCTCAGGCTGGAGTGCA ATATAAAATAATTTTTTTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCTCAGGCTGGAGTGCA T C PUM1 Ensembl:ENSG00000134644 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1162499612 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121030,RMVar_hsa_circ_130983,RMVar_hsa_circ_124647,RMVar_hsa_circ_371999,RMVar_hsa_circ_348445,RMVar_hsa_circ_278509,RMVar_hsa_circ_36810,RMVar_hsa_circ_83915,RMVar_hsa_circ_130984,RMVar_hsa_circ_130985,RMVar_hsa_circ_130986,RMVar_hsa_circ_315757,RMVar_hsa_circ_327662,RMVar_hsa_circ_372758,RMVar_hsa_circ_320131,RMVar_hsa_circ_312856,RMVar_hsa_circ_298189,RMVar_hsa_circ_306228,RMVar_hsa_circ_130987,RMVar_hsa_circ_130989,RMVar_hsa_circ_130990,RMVar_hsa_circ_130988,RMVar_hsa_circ_109101,RMVar_hsa_circ_116545,RMVar_hsa_circ_86432,RMVar_hsa_circ_130993,RMVar_hsa_circ_78901,RMVar_hsa_circ_130995,RMVar_hsa_circ_130996,RMVar_hsa_circ_130997,RMVar_hsa_circ_130994,RMVar_hsa_circ_86246,RMVar_hsa_circ_338078,RMVar_hsa_circ_372401,RMVar_hsa_circ_346873,RMVar_hsa_circ_274987,RMVar_hsa_circ_67706,RMVar_hsa_circ_130999,RMVar_hsa_circ_25419,RMVar_hsa_circ_31601,RMVar_hsa_circ_131000,RMVar_hsa_circ_131001,RMVar_hsa_circ_130998 30846 RMVar_ID_30846 Human_SNP_ID_8158794 A-to-I Human chr1 - 30947996 30947996 30947996 AAAAAGTTGGCTGGGCATGGTGGTGCACTCCTATAGTCTCAGCTGCTTGGGGTGCTAAGGCAGGA AAAAAGTTGGCTGGGCATGGTGGTGCACTCCTGTAGTCTCAGCTGCTTGGGGTGCTAAGGCAGGA T C PUM1 Ensembl:ENSG00000134644 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs751725792 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22861822,Human_RBP_ID_24682321 RMVar_hsa_circ_121030,RMVar_hsa_circ_130983,RMVar_hsa_circ_124647,RMVar_hsa_circ_371999,RMVar_hsa_circ_348445,RMVar_hsa_circ_278509,RMVar_hsa_circ_36810,RMVar_hsa_circ_83915,RMVar_hsa_circ_130984,RMVar_hsa_circ_130985,RMVar_hsa_circ_130986,RMVar_hsa_circ_315757,RMVar_hsa_circ_327662,RMVar_hsa_circ_372758,RMVar_hsa_circ_320131,RMVar_hsa_circ_312856,RMVar_hsa_circ_298189,RMVar_hsa_circ_306228,RMVar_hsa_circ_130987,RMVar_hsa_circ_130989,RMVar_hsa_circ_130990,RMVar_hsa_circ_130988,RMVar_hsa_circ_109101,RMVar_hsa_circ_116545,RMVar_hsa_circ_86432,RMVar_hsa_circ_130993,RMVar_hsa_circ_78901,RMVar_hsa_circ_130995,RMVar_hsa_circ_130996,RMVar_hsa_circ_130997,RMVar_hsa_circ_130994,RMVar_hsa_circ_86246,RMVar_hsa_circ_338078,RMVar_hsa_circ_372401,RMVar_hsa_circ_346873,RMVar_hsa_circ_274987,RMVar_hsa_circ_67706,RMVar_hsa_circ_130999,RMVar_hsa_circ_25419,RMVar_hsa_circ_31601,RMVar_hsa_circ_131000,RMVar_hsa_circ_131001,RMVar_hsa_circ_130998 30847 RMVar_ID_30847 Human_SNP_ID_8158808 A-to-I Human chr1 - 30948047 30948047 30948047 GCCCAGGAGTTTGAGACCAGCCTGGGCAGCATAGTGAAACCCCATCTCTATAAAAAGTTGGCTGG GCCCAGGAGTTTGAGACCAGCCTGGGCAGCATGGTGAAACCCCATCTCTATAAAAAGTTGGCTGG T C PUM1 Ensembl:ENSG00000134644 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs113906977 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24682324 RMVar_hsa_circ_121030,RMVar_hsa_circ_130983,RMVar_hsa_circ_124647,RMVar_hsa_circ_371999,RMVar_hsa_circ_348445,RMVar_hsa_circ_278509,RMVar_hsa_circ_36810,RMVar_hsa_circ_83915,RMVar_hsa_circ_130984,RMVar_hsa_circ_130985,RMVar_hsa_circ_130986,RMVar_hsa_circ_315757,RMVar_hsa_circ_327662,RMVar_hsa_circ_372758,RMVar_hsa_circ_320131,RMVar_hsa_circ_312856,RMVar_hsa_circ_298189,RMVar_hsa_circ_306228,RMVar_hsa_circ_130987,RMVar_hsa_circ_130989,RMVar_hsa_circ_130990,RMVar_hsa_circ_130988,RMVar_hsa_circ_109101,RMVar_hsa_circ_116545,RMVar_hsa_circ_86432,RMVar_hsa_circ_130993,RMVar_hsa_circ_78901,RMVar_hsa_circ_130995,RMVar_hsa_circ_130996,RMVar_hsa_circ_130997,RMVar_hsa_circ_130994,RMVar_hsa_circ_86246,RMVar_hsa_circ_338078,RMVar_hsa_circ_372401,RMVar_hsa_circ_346873,RMVar_hsa_circ_274987,RMVar_hsa_circ_67706,RMVar_hsa_circ_130999,RMVar_hsa_circ_25419,RMVar_hsa_circ_31601,RMVar_hsa_circ_131000,RMVar_hsa_circ_131001,RMVar_hsa_circ_130998 30848 RMVar_ID_30848 Human_SNP_ID_8158941 A-to-I Human chr1 - 30948651 30948651 30948651 AACCTCCTGAGCTCAAGTGGTCCTCCCATCTTAGCCTCCTGAGTAGCTGGAACTACAGGCATACG AACCTCCTGAGCTCAAGTGGTCCTCCCATCTTGGCCTCCTGAGTAGCTGGAACTACAGGCATACG T C PUM1 Ensembl:ENSG00000134644 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs369498709 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121030,RMVar_hsa_circ_130983,RMVar_hsa_circ_124647,RMVar_hsa_circ_371999,RMVar_hsa_circ_348445,RMVar_hsa_circ_278509,RMVar_hsa_circ_36810,RMVar_hsa_circ_83915,RMVar_hsa_circ_130984,RMVar_hsa_circ_130985,RMVar_hsa_circ_130986,RMVar_hsa_circ_315757,RMVar_hsa_circ_327662,RMVar_hsa_circ_372758,RMVar_hsa_circ_320131,RMVar_hsa_circ_312856,RMVar_hsa_circ_298189,RMVar_hsa_circ_306228,RMVar_hsa_circ_130987,RMVar_hsa_circ_130989,RMVar_hsa_circ_130990,RMVar_hsa_circ_130988,RMVar_hsa_circ_109101,RMVar_hsa_circ_116545,RMVar_hsa_circ_86432,RMVar_hsa_circ_130993,RMVar_hsa_circ_78901,RMVar_hsa_circ_130995,RMVar_hsa_circ_130996,RMVar_hsa_circ_130997,RMVar_hsa_circ_130994,RMVar_hsa_circ_86246,RMVar_hsa_circ_338078,RMVar_hsa_circ_372401,RMVar_hsa_circ_346873,RMVar_hsa_circ_274987,RMVar_hsa_circ_67706,RMVar_hsa_circ_130999,RMVar_hsa_circ_25419,RMVar_hsa_circ_31601,RMVar_hsa_circ_131000,RMVar_hsa_circ_131001,RMVar_hsa_circ_130998 30849 RMVar_ID_30849 Human_SNP_ID_8158957 A-to-I Human chr1 - 30948743 30948743 30948743 TTCTTGTTTTTCTTTCTTTCTTTTTGGAGACAAGGTCTCACTCTGTCACCCAGGCTGGAGTGCAG TTCTTGTTTTTCTTTCTTTCTTTTTGGAGACAGGGTCTCACTCTGTCACCCAGGCTGGAGTGCAG T C PUM1 Ensembl:ENSG00000134644 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1557548848 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10926223,Human_RBP_ID_19337483 RMVar_hsa_circ_121030,RMVar_hsa_circ_130983,RMVar_hsa_circ_124647,RMVar_hsa_circ_371999,RMVar_hsa_circ_348445,RMVar_hsa_circ_278509,RMVar_hsa_circ_36810,RMVar_hsa_circ_83915,RMVar_hsa_circ_130984,RMVar_hsa_circ_130985,RMVar_hsa_circ_130986,RMVar_hsa_circ_315757,RMVar_hsa_circ_327662,RMVar_hsa_circ_372758,RMVar_hsa_circ_320131,RMVar_hsa_circ_312856,RMVar_hsa_circ_298189,RMVar_hsa_circ_306228,RMVar_hsa_circ_130987,RMVar_hsa_circ_130989,RMVar_hsa_circ_130990,RMVar_hsa_circ_130988,RMVar_hsa_circ_109101,RMVar_hsa_circ_116545,RMVar_hsa_circ_86432,RMVar_hsa_circ_130993,RMVar_hsa_circ_78901,RMVar_hsa_circ_130995,RMVar_hsa_circ_130996,RMVar_hsa_circ_130997,RMVar_hsa_circ_130994,RMVar_hsa_circ_86246,RMVar_hsa_circ_338078,RMVar_hsa_circ_372401,RMVar_hsa_circ_346873,RMVar_hsa_circ_274987,RMVar_hsa_circ_67706,RMVar_hsa_circ_130999,RMVar_hsa_circ_25419,RMVar_hsa_circ_31601,RMVar_hsa_circ_131000,RMVar_hsa_circ_131001,RMVar_hsa_circ_130998 30850 RMVar_ID_30850 Human_SNP_ID_8164205 A-to-I Human chr1 - 30969929 30969929 30969929 CTGGGCTCAGTGGCTTCACACTTGTAATCCCAACACTTTGGCAGGCCAAGGCAGGTGGATTGCTT CTGGGCTCAGTGGCTTCACACTTGTAATCCCAGCACTTTGGCAGGCCAAGGCAGGTGGATTGCTT T C PUM1 Ensembl:ENSG00000134644 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs536584959 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36810,RMVar_hsa_circ_83915,RMVar_hsa_circ_372758,RMVar_hsa_circ_298189,RMVar_hsa_circ_306228,RMVar_hsa_circ_130987,RMVar_hsa_circ_116545,RMVar_hsa_circ_130996,RMVar_hsa_circ_130997,RMVar_hsa_circ_86246,RMVar_hsa_circ_372401,RMVar_hsa_circ_67706,RMVar_hsa_circ_131000,RMVar_hsa_circ_131001,RMVar_hsa_circ_111157,RMVar_hsa_circ_42188,RMVar_hsa_circ_101691,RMVar_hsa_circ_131005,RMVar_hsa_circ_131002,RMVar_hsa_circ_319793,RMVar_hsa_circ_308339,RMVar_hsa_circ_282966,RMVar_hsa_circ_296277,RMVar_hsa_circ_118316,RMVar_hsa_circ_71922,RMVar_hsa_circ_53855,RMVar_hsa_circ_131009,RMVar_hsa_circ_131011,RMVar_hsa_circ_131012,RMVar_hsa_circ_131013,RMVar_hsa_circ_131010,RMVar_hsa_circ_131015,RMVar_hsa_circ_116197,RMVar_hsa_circ_344707,RMVar_hsa_circ_346734,RMVar_hsa_circ_310067,RMVar_hsa_circ_80535,RMVar_hsa_circ_131014 30851 RMVar_ID_30851 Human_SNP_ID_8166045 A-to-I Human chr1 - 30976005 30976005 30976005 TGGCTCACTGTAACCTCTGCCTCCTGGGTTCAAGCAGTTCTCCTGCCTCAGCCTTCCGAGTAGCT TGGCTCACTGTAACCTCTGCCTCCTGGGTTCACGCAGTTCTCCTGCCTCAGCCTTCCGAGTAGCT T G PUM1 Ensembl:ENSG00000134644 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444509781 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36810,RMVar_hsa_circ_83915,RMVar_hsa_circ_372758,RMVar_hsa_circ_298189,RMVar_hsa_circ_130987,RMVar_hsa_circ_116545,RMVar_hsa_circ_130996,RMVar_hsa_circ_130997,RMVar_hsa_circ_86246,RMVar_hsa_circ_372401,RMVar_hsa_circ_67706,RMVar_hsa_circ_131000,RMVar_hsa_circ_131001,RMVar_hsa_circ_111157,RMVar_hsa_circ_45672,RMVar_hsa_circ_42188,RMVar_hsa_circ_101691,RMVar_hsa_circ_131005,RMVar_hsa_circ_131002,RMVar_hsa_circ_319793,RMVar_hsa_circ_282966,RMVar_hsa_circ_296277,RMVar_hsa_circ_118316,RMVar_hsa_circ_71922,RMVar_hsa_circ_53855,RMVar_hsa_circ_131011,RMVar_hsa_circ_131012,RMVar_hsa_circ_131013,RMVar_hsa_circ_131010,RMVar_hsa_circ_131015,RMVar_hsa_circ_116197,RMVar_hsa_circ_346734,RMVar_hsa_circ_310067,RMVar_hsa_circ_80535,RMVar_hsa_circ_307848,RMVar_hsa_circ_363880,RMVar_hsa_circ_131014,RMVar_hsa_circ_298803,RMVar_hsa_circ_131017,RMVar_hsa_circ_131018,RMVar_hsa_circ_131019 30852 RMVar_ID_30852 Human_SNP_ID_8171484 A-to-I Human chr1 - 30999251 30999251 30999251 TCACACTTGTAATCACAGAGCTTTGGGAGACCAAGGCAGGAGGATCACTTGAAGCCAGGTGTTTG TCACACTTGTAATCACAGAGCTTTGGGAGACCTAGGCAGGAGGATCACTTGAAGCCAGGTGTTTG T A PUM1 Ensembl:ENSG00000134644 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1343474452 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83915,RMVar_hsa_circ_372758,RMVar_hsa_circ_130987,RMVar_hsa_circ_130997,RMVar_hsa_circ_86246,RMVar_hsa_circ_131001,RMVar_hsa_circ_111157,RMVar_hsa_circ_45672,RMVar_hsa_circ_131002,RMVar_hsa_circ_71922,RMVar_hsa_circ_53855,RMVar_hsa_circ_46483,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_131025,RMVar_hsa_circ_116734,RMVar_hsa_circ_275323,RMVar_hsa_circ_355888,RMVar_hsa_circ_379111,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 30853 RMVar_ID_30853 Human_SNP_ID_8179962 A-to-I Human chr1 - 31033561 31033561 31033561 AGGGCTTCGAGACCTGCCTGGGCAACATGGTAAAACCTCGTCTTCTTCAAAAAATATGAAAATTA AGGGCTTCGAGACCTGCCTGGGCAACATGGTAGAACCTCGTCTTCTTCAAAAAATATGAAAATTA T C PUM1 Ensembl:ENSG00000134644 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs780811734 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_97110 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 30854 RMVar_ID_30854 Human_SNP_ID_8179986 A-to-I Human chr1 - 31033670 31033670 31033670 GTAACAGAGCCAGACCCTGTCTCAAAAAAATAAAATGGGCTGGGCGTGGTGGCTAACACCTGTAA GTAACAGAGCCAGACCCTGTCTCAAAAAAATAGAATGGGCTGGGCGTGGTGGCTAACACCTGTAA T C PUM1 Ensembl:ENSG00000134644 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs867709847 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10930047 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 30855 RMVar_ID_30855 Human_SNP_ID_8179987 A-to-I Human chr1 - 31033671 31033671 31033671 GGTAACAGAGCCAGACCCTGTCTCAAAAAAATAAAATGGGCTGGGCGTGGTGGCTAACACCTGTA GGTAACAGAGCCAGACCCTGTCTCAAAAAAATTAAATGGGCTGGGCGTGGTGGCTAACACCTGTA T A PUM1 Ensembl:ENSG00000134644 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1468938995 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10930047 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 30856 RMVar_ID_30856 Human_SNP_ID_8180693 A-to-I Human chr1 - 31036464 31036464 31036464 TCAAGTGATCCTCCTGCCTTGGCCTCGAAAGTACTGGCCATGTAGAGGTGTGAGCCACCCTGTAT TCAAGTGATCCTCCTGCCTTGGCCTCGAAAGTGCTGGCCATGTAGAGGTGTGAGCCACCCTGTAT T C PUM1 Ensembl:ENSG00000134644 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1309020043 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10930124,Human_RBP_ID_23303429 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 30857 RMVar_ID_30857 Human_SNP_ID_8181828 A-to-I Human chr1 - 31039812 31039812 31039812 TCACTGCAGCCTCTGCCTCCTGGGTTCAAGCGATTATCCTGCCACAGCCTCCCAGGTAGCTGGGA TCACTGCAGCCTCTGCCTCCTGGGTTCAAGCGTTTATCCTGCCACAGCCTCCCAGGTAGCTGGGA T A PUM1 Ensembl:ENSG00000134644 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1356708014 Functional Loss SNV dbSNP153 33..33 33 - - - 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 30858 RMVar_ID_30858 Human_SNP_ID_8182695 A-to-I Human chr1 - 31043343 31043343 31043343 AAAAATTAGCCGGACATGATGGGGGGGTGCCTATAATCCCAGGTTCTCAGGTGGCTGAGGCAGGA AAAAATTAGCCGGACATGATGGGGGGGTGCCTGTAATCCCAGGTTCTCAGGTGGCTGAGGCAGGA T C PUM1 Ensembl:ENSG00000134644 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1411920089 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10930359 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 30859 RMVar_ID_30859 Human_SNP_ID_8182971 A-to-I Human chr1 - 31044350 31044350 31044350 TCGCCCAGGCTGGAGTGCAGTGGCACGATCTCAGCTCACTGCAGGCTCCGCCCCCTGGGGTTCCC TCGCCCAGGCTGGAGTGCAGTGGCACGATCTCGGCTCACTGCAGGCTCCGCCCCCTGGGGTTCCC T C PUM1 Ensembl:ENSG00000134644 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1255293866 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8307915 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 30860 RMVar_ID_30860 Human_SNP_ID_8183493 A-to-I Human chr1 - 31046300 31046300 31046300 CTCACCGCAACCTCCACCTCCCGGGTTCAAGCAATTCTCCTGCCTTAGCCTCCCGAGTAGCTGTG CTCACCGCAACCTCCACCTCCCGGGTTCAAGCGATTCTCCTGCCTTAGCCTCCCGAGTAGCTGTG T C PUM1 Ensembl:ENSG00000134644 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1255879951 Functional Loss SNV dbSNP153 33..33 33 - - - 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 30861 RMVar_ID_30861 Human_SNP_ID_8183725 A-to-I Human chr1 - 31046973 31046973 31046973 TTGGCCAGGCTGATTTTTGAACTCCTGACCTTATGATCCACCCGCCTTGGCCTTCCAAAGTGCTG TTGGCCAGGCTGATTTTTGAACTCCTGACCTTGTGATCCACCCGCCTTGGCCTTCCAAAGTGCTG T C PUM1 Ensembl:ENSG00000134644 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs776937824 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10930441,Human_RBP_ID_17557076 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 30862 RMVar_ID_30862 Human_SNP_ID_8184476 A-to-I Human chr1 - 31049597 31049597 31049597 CAGATCACTGCAACCTCTTCCTCCTGGGTTCAAGCAGTTCTCCTGCTTCAGCCTCCCAAGCAGTT CAGATCACTGCAACCTCTTCCTCCTGGGTTCATGCAGTTCTCCTGCTTCAGCCTCCCAAGCAGTT T A PUM1 Ensembl:ENSG00000134644 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1050887870 Functional Loss SNV dbSNP153 33..33 33 - - - 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 30863 RMVar_ID_30863 Human_SNP_ID_8184477 A-to-I Human chr1 - 31049597 31049597 31049597 CAGATCACTGCAACCTCTTCCTCCTGGGTTCAAGCAGTTCTCCTGCTTCAGCCTCCCAAGCAGTT CAGATCACTGCAACCTCTTCCTCCTGGGTTCAGGCAGTTCTCCTGCTTCAGCCTCCCAAGCAGTT T C PUM1 Ensembl:ENSG00000134644 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1050887870 Functional Loss SNV dbSNP153 33..33 33 - - - 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 30864 RMVar_ID_30864 Human_SNP_ID_8184577 A-to-I Human chr1 - 31049958 31049958 31049958 AGGTGTGTTGGCGGGTGCCTGTGGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCACTTGAA AGGTGTGTTGGCGGGTGCCTGTGGTCCCAGCTGCTTGGGAGGCTGAGGCAGGAGAATCACTTGAA T C PUM1 Ensembl:ENSG00000134644 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1413804253 Functional Loss SNV dbSNP153 33..33 33 - - - 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 30865 RMVar_ID_30865 Human_SNP_ID_8184656 A-to-I Human chr1 - 31050237 31050237 31050237 CAAGCAGTCCTCGCACCTTGGCCTCCCAAAGTACTGAGATTAAAAGTGTGAGCCACGTACCTGGC CAAGCAGTCCTCGCACCTTGGCCTCCCAAAGTGCTGAGATTAAAAGTGTGAGCCACGTACCTGGC T C PUM1 Ensembl:ENSG00000134644 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1251392016 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17556603 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 30866 RMVar_ID_30866 Human_SNP_ID_8184673 A-to-I Human chr1 - 31050302 31050302 31050302 TTTTGTATTTTTAGTAGAGACAGGGTTTCACAATGTTGTCCAGGCTGGTTTTAAACTCCTGGTCT TTTTGTATTTTTAGTAGAGACAGGGTTTCACAGTGTTGTCCAGGCTGGTTTTAAACTCCTGGTCT T C PUM1 Ensembl:ENSG00000134644 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs907037982 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10930522,Human_RBP_ID_17556603 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 30867 RMVar_ID_30867 Human_SNP_ID_8184680 A-to-I Human chr1 - 31050337 31050337 31050337 GGGATTACAGGGGTGTACCACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCA GGGATTACAGGGGTGTACCACCATGCCTGGCTGATTTTTGTATTTTTAGTAGAGACAGGGTTTCA T C PUM1 Ensembl:ENSG00000134644 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1476275337 Functional Loss SNV dbSNP153 33..33 33 - - - 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 30868 RMVar_ID_30868 Human_SNP_ID_8184983 A-to-I Human chr1 - 31051491 31051491 31051491 GGAGACCAGCCTGACCAACATGGAGAAACCCCATCTCTACAAAAAATACAAAATTAGTGGGGCGT GGAGACCAGCCTGACCAACATGGAGAAACCCCGTCTCTACAAAAAATACAAAATTAGTGGGGCGT T C PUM1 Ensembl:ENSG00000134644 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs987247014 Functional Loss SNV dbSNP153 33..33 33 - - - 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 30869 RMVar_ID_30869 Human_SNP_ID_8185552 A-to-I Human chr1 - 31053634 31053634 31053634 TCATGTCTCTACAAAATATACAGAAATTAGCCAGGCATGGTGGCGCTGTGCCTGTGGTCCCAGCT TCATGTCTCTACAAAATATACAGAAATTAGCCTGGCATGGTGGCGCTGTGCCTGTGGTCCCAGCT T A PUM1 Ensembl:ENSG00000134644 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs543079218 Functional Loss SNV dbSNP153 33..33 33 - - - 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 30870 RMVar_ID_30870 Human_SNP_ID_8185579 A-to-I Human chr1 - 31053755 31053753 31053755 TTTTCATTTTTTGGCTGGACGCAGTGGCTCACACCTGTAATCGCAGCACTTTGGGAGGCTGAGGA TTTTCATTTTTTGGCTGGACGCAGTGGCTCAC__CTGTAATCGCAGCACTTTGGGAGGCTGAGGA GGT G PUM1 Ensembl:ENSG00000134644 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1289917395 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_17557081 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 30871 RMVar_ID_30871 Human_SNP_ID_8185735 A-to-I Human chr1 - 31054183 31054183 31054183 TCCTGGGACCACAGGCACACGTCACAACACCTAGCTCATCTTTGTATTTTTTGTAGAGGTGGAGT TCCTGGGACCACAGGCACACGTCACAACACCTTGCTCATCTTTGTATTTTTTGTAGAGGTGGAGT T A PUM1 Ensembl:ENSG00000134644 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs913568693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5809221 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 30872 RMVar_ID_30872 Human_SNP_ID_8185755 A-to-I Human chr1 - 31054287 31054287 31054287 GGTTTCACTCCTGTTGCCGAGGCTGGAGTGCAATGGGCACCATCTAGGCTCACTGCAACCTCTGC GGTTTCACTCCTGTTGCCGAGGCTGGAGTGCAGTGGGCACCATCTAGGCTCACTGCAACCTCTGC T C PUM1 Ensembl:ENSG00000134644 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs899778538 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5809222,Human_RBP_ID_10930637,Human_RBP_ID_17557762,Human_RBP_ID_23303968 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 30873 RMVar_ID_30873 Human_SNP_ID_8186393 A-to-I Human chr1 - 31056698 31056698 31056698 TGCTTGAGCGTGGGTGGCAGAAGTTGCAGTGAACAGAGATCATGCCACTGCACTTCAGCCTGGGC TGCTTGAGCGTGGGTGGCAGAAGTTGCAGTGAGCAGAGATCATGCCACTGCACTTCAGCCTGGGC T C PUM1 Ensembl:ENSG00000134644 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1169512718 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557082,Human_RBP_ID_22470041,Human_RBP_ID_23148730 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 30874 RMVar_ID_30874 Human_SNP_ID_8186444 A-to-I Human chr1 - 31056914 31056914 31056914 GTGGCGCATGCTTGTAATCCCAGCTACTTGGAAGGCTGAGGCAGGAGAGTCACTTGAACCTGGGA GTGGCGCATGCTTGTAATCCCAGCTACTTGGACGGCTGAGGCAGGAGAGTCACTTGAACCTGGGA T G PUM1 Ensembl:ENSG00000134644 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1034188716 Functional Loss SNV dbSNP153 33..33 33 - - - 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 30875 RMVar_ID_30875 Human_SNP_ID_8197013 A-to-I Human chr1 + 31094935 31094935 31094935 ATGAGACATTTCAGTTCTTCCTGTCATGAAGCATCTGCTGAGAGGAGCTGGGTCAAGGTCCCTGG ATGAGACATTTCAGTTCTTCCTGTCATGAAGCGTCTGCTGAGAGGAGCTGGGTCAAGGTCCCTGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560755725 Functional Loss SNV dbSNP153 33..33 33 - - - 30876 RMVar_ID_30876 Human_SNP_ID_8197014 A-to-I Human chr1 + 31094935 31094935 31094935 ATGAGACATTTCAGTTCTTCCTGTCATGAAGCATCTGCTGAGAGGAGCTGGGTCAAGGTCCCTGG ATGAGACATTTCAGTTCTTCCTGTCATGAAGCTTCTGCTGAGAGGAGCTGGGTCAAGGTCCCTGG A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560755725 Functional Loss SNV dbSNP153 33..33 33 - - - 30877 RMVar_ID_30877 Human_SNP_ID_8197017 A-to-I Human chr1 + 31094948 31094948 31094948 GTTCTTCCTGTCATGAAGCATCTGCTGAGAGGAGCTGGGTCAAGGTCCCTGGACTCTGCCTTCAG GTTCTTCCTGTCATGAAGCATCTGCTGAGAGGGGCTGGGTCAAGGTCCCTGGACTCTGCCTTCAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878936361 Functional Loss SNV dbSNP153 33..33 33 - - - 30878 RMVar_ID_30878 Human_SNP_ID_8197026 A-to-I Human chr1 + 31094984 31094984 31094984 GGGTCAAGGTCCCTGGACTCTGCCTTCAGGGCACATTAGCCCTGAGCCAAGGCAGCTTTGATGGC GGGTCAAGGTCCCTGGACTCTGCCTTCAGGGCGCATTAGCCCTGAGCCAAGGCAGCTTTGATGGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879208758 Functional Loss SNV dbSNP153 33..33 33 - - - 30879 RMVar_ID_30879 Human_SNP_ID_8197034 A-to-I Human chr1 + 31095005 31095005 31095005 GCCTTCAGGGCACATTAGCCCTGAGCCAAGGCAGCTTTGATGGCAGCCACCAGCTTCAGAAACTT GCCTTCAGGGCACATTAGCCCTGAGCCAAGGCGGCTTTGATGGCAGCCACCAGCTTCAGAAACTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879130793 Functional Loss SNV dbSNP153 33..33 33 - - - 30880 RMVar_ID_30880 Human_SNP_ID_8197048 A-to-I Human chr1 + 31095053 31095053 31095053 ACCAGCTTCAGAAACTTGTTTTCTGTGTCCACATAGCCATCACCTTTCTTCTTAGAGTGAATCAA ACCAGCTTCAGAAACTTGTTTTCTGTGTCCACGTAGCCATCACCTTTCTTCTTAGAGTGAATCAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1033152147 Functional Loss SNV dbSNP153 33..33 33 - - - 30881 RMVar_ID_30881 Human_SNP_ID_8197051 A-to-I Human chr1 + 31095062 31095062 31095062 AGAAACTTGTTTTCTGTGTCCACATAGCCATCACCTTTCTTCTTAGAGTGAATCAACTTCCCAGC AGAAACTTGTTTTCTGTGTCCACATAGCCATCGCCTTTCTTCTTAGAGTGAATCAACTTCCCAGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879030380 Functional Loss SNV dbSNP153 33..33 33 - - - 30882 RMVar_ID_30882 Human_SNP_ID_8197056 A-to-I Human chr1 + 31095092 31095092 31095092 TCACCTTTCTTCTTAGAGTGAATCAACTTCCCAGCTACCATTACGTCAAAGAACCCGGTGGCCTG TCACCTTTCTTCTTAGAGTGAATCAACTTCCCGGCTACCATTACGTCAAAGAACCCGGTGGCCTG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878954617 Functional Loss SNV dbSNP153 33..33 33 - - - 30883 RMVar_ID_30883 Human_SNP_ID_8197067 A-to-I Human chr1 - 31095136 31095136 31095136 ATGAGTTCCTCTGGACTTTGGACATCTGCAGCAAGGGAACTCCCCAGGCCACCGGGTTCTTTGAC ATGAGTTCCTCTGGACTTTGGACATCTGCAGCGAGGGAACTCCCCAGGCCACCGGGTTCTTTGAC T C SELENOWP1 Ensembl:ENSG00000215900 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs920895707 Functional Loss SNV dbSNP153 33..33 33 - - - 30884 RMVar_ID_30884 Human_SNP_ID_8197068 A-to-I Human chr1 - 31095139 31095139 31095139 AAGATGAGTTCCTCTGGACTTTGGACATCTGCAGCAAGGGAACTCCCCAGGCCACCGGGTTCTTT AAGATGAGTTCCTCTGGACTTTGGACATCTGCTGCAAGGGAACTCCCCAGGCCACCGGGTTCTTT T A SELENOWP1 Ensembl:ENSG00000215900 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs953789061 Functional Loss SNV dbSNP153 33..33 33 - - - 30885 RMVar_ID_30885 Human_SNP_ID_8197069 A-to-I Human chr1 - 31095139 31095139 31095139 AAGATGAGTTCCTCTGGACTTTGGACATCTGCAGCAAGGGAACTCCCCAGGCCACCGGGTTCTTT AAGATGAGTTCCTCTGGACTTTGGACATCTGCGGCAAGGGAACTCCCCAGGCCACCGGGTTCTTT T C SELENOWP1 Ensembl:ENSG00000215900 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs953789061 Functional Loss SNV dbSNP153 33..33 33 - - - 30886 RMVar_ID_30886 Human_SNP_ID_8241965 A-to-I Human chr1 - 31262357 31262357 31262357 GCTACCACTCCTGGCTAATTTTTTGTATTTTTAGTAGAGACTGGGTTTCACCTTGTTGGCCAGGC GCTACCACTCCTGGCTAATTTTTTGTATTTTTTGTAGAGACTGGGTTTCACCTTGTTGGCCAGGC T A SNRNP40 Ensembl:ENSG00000060688 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1486493171 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1173,RMVar_hsa_circ_77241,RMVar_hsa_circ_38215,RMVar_hsa_circ_79760,RMVar_hsa_circ_131047,RMVar_hsa_circ_304438,RMVar_hsa_circ_50169,RMVar_hsa_circ_8040,RMVar_hsa_circ_131048,RMVar_hsa_circ_131049 30887 RMVar_ID_30887 Human_SNP_ID_8242129 A-to-I Human chr1 - 31262761 31262761 31262761 CAAGCCTTGGCCCCCCAAAGTGCTAGGATTACAGATGTGAGCCACCATGCCCAGCCTCATAATTT CAAGCCTTGGCCCCCCAAAGTGCTAGGATTACCGATGTGAGCCACCATGCCCAGCCTCATAATTT T G SNRNP40 Ensembl:ENSG00000060688 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1438169474 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1173,RMVar_hsa_circ_77241,RMVar_hsa_circ_38215,RMVar_hsa_circ_79760,RMVar_hsa_circ_131047,RMVar_hsa_circ_304438,RMVar_hsa_circ_50169,RMVar_hsa_circ_8040,RMVar_hsa_circ_131048,RMVar_hsa_circ_131049 30888 RMVar_ID_30888 Human_SNP_ID_8242269 A-to-I Human chr1 - 31263276 31263276 31263276 TATGTAGACTTTTGTGAAAATTATGGCCTGTGATGATAAAAATACTGGCTCTAATACTATAGAAT TATGTAGACTTTTGTGAAAATTATGGCCTGTGGTGATAAAAATACTGGCTCTAATACTATAGAAT T C SNRNP40,AC114495.2 Ensembl:ENSG00000060688,Ensembl:ENSG00000229447 Protein coding,Pseudogene intron,exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs12725881 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11176251 GWAS_ID_3440,GWAS_ID_3441,GWAS_ID_3442,GWAS_ID_3443,GWAS_ID_3444,GWAS_ID_3445 RMVar_hsa_circ_1173,RMVar_hsa_circ_77241,RMVar_hsa_circ_38215,RMVar_hsa_circ_79760,RMVar_hsa_circ_131047,RMVar_hsa_circ_304438,RMVar_hsa_circ_50169,RMVar_hsa_circ_8040,RMVar_hsa_circ_131048,RMVar_hsa_circ_131049 30889 RMVar_ID_30889 Human_SNP_ID_8242461 A-to-I Human chr1 - 31263953 31263953 31263953 TCTATACTTTACCCTTTAATGACTTAAGCAAGATTGAGGGTCAAAGGAACTTTTTTTTTTTTTTT TCTATACTTTACCCTTTAATGACTTAAGCAAGTTTGAGGGTCAAAGGAACTTTTTTTTTTTTTTT T A SNRNP40 Ensembl:ENSG00000060688 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4949202 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5809397 GWAS_ID_3446,GWAS_ID_3447,GWAS_ID_3448,GWAS_ID_3449,GWAS_ID_3450,GWAS_ID_3451,GWAS_ID_3452,GWAS_ID_3453,GWAS_ID_3454,GWAS_ID_3455,GWAS_ID_3456,GWAS_ID_3457,GWAS_ID_3458,GWAS_ID_3459,GWAS_ID_3460,GWAS_ID_3461,GWAS_ID_3462,GWAS_ID_3463,GWAS_ID_3464,GWAS_ID_3465,GWAS_ID_3466,GWAS_ID_3467,GWAS_ID_3468,GWAS_ID_3469,GWAS_ID_3470,GWAS_ID_3471,GWAS_ID_3472,GWAS_ID_3473,GWAS_ID_3474,GWAS_ID_3475,GWAS_ID_3476,GWAS_ID_3477,GWAS_ID_3478,GWAS_ID_3479,GWAS_ID_3480,GWAS_ID_3481,GWAS_ID_3482,GWAS_ID_3483,GWAS_ID_3484,GWAS_ID_3485,GWAS_ID_3486 RMVar_hsa_circ_1173,RMVar_hsa_circ_77241,RMVar_hsa_circ_38215,RMVar_hsa_circ_79760,RMVar_hsa_circ_131047,RMVar_hsa_circ_304438,RMVar_hsa_circ_50169,RMVar_hsa_circ_8040,RMVar_hsa_circ_131048,RMVar_hsa_circ_131049 30890 RMVar_ID_30890 Human_SNP_ID_8242462 A-to-I Human chr1 - 31263953 31263953 31263953 TCTATACTTTACCCTTTAATGACTTAAGCAAGATTGAGGGTCAAAGGAACTTTTTTTTTTTTTTT TCTATACTTTACCCTTTAATGACTTAAGCAAGGTTGAGGGTCAAAGGAACTTTTTTTTTTTTTTT T C SNRNP40 Ensembl:ENSG00000060688 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4949202 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5809397 GWAS_ID_3446,GWAS_ID_3447,GWAS_ID_3448,GWAS_ID_3449,GWAS_ID_3450,GWAS_ID_3451,GWAS_ID_3452,GWAS_ID_3453,GWAS_ID_3454,GWAS_ID_3455,GWAS_ID_3456,GWAS_ID_3457,GWAS_ID_3458,GWAS_ID_3459,GWAS_ID_3460,GWAS_ID_3461,GWAS_ID_3462,GWAS_ID_3463,GWAS_ID_3464,GWAS_ID_3465,GWAS_ID_3466,GWAS_ID_3467,GWAS_ID_3468,GWAS_ID_3469,GWAS_ID_3470,GWAS_ID_3471,GWAS_ID_3472,GWAS_ID_3473,GWAS_ID_3474,GWAS_ID_3475,GWAS_ID_3476,GWAS_ID_3477,GWAS_ID_3478,GWAS_ID_3479,GWAS_ID_3480,GWAS_ID_3481,GWAS_ID_3482,GWAS_ID_3483,GWAS_ID_3484,GWAS_ID_3485,GWAS_ID_3486 RMVar_hsa_circ_1173,RMVar_hsa_circ_77241,RMVar_hsa_circ_38215,RMVar_hsa_circ_79760,RMVar_hsa_circ_131047,RMVar_hsa_circ_304438,RMVar_hsa_circ_50169,RMVar_hsa_circ_8040,RMVar_hsa_circ_131048,RMVar_hsa_circ_131049 30891 RMVar_ID_30891 Human_SNP_ID_8242862 A-to-I Human chr1 - 31265826 31265826 31265826 TAAATTTTTGTTTGTTTTTGAGATGTAGTCTCACTCTGTCGCCCAGGCTGGAGTGCAGTGGTGCA TAAATTTTTGTTTGTTTTTGAGATGTAGTCTCTCTCTGTCGCCCAGGCTGGAGTGCAGTGGTGCA T A SNRNP40 Ensembl:ENSG00000060688 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs907017770 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1173,RMVar_hsa_circ_77241,RMVar_hsa_circ_38215,RMVar_hsa_circ_79760,RMVar_hsa_circ_131047,RMVar_hsa_circ_304438,RMVar_hsa_circ_50169,RMVar_hsa_circ_8040,RMVar_hsa_circ_131048,RMVar_hsa_circ_131049 30892 RMVar_ID_30892 Human_SNP_ID_8243272 A-to-I Human chr1 - 31267674 31267674 31267674 AAAATTAGCCGGGCGTGGCGGCACATGCCTGTAATCCCAGCTACTCAGGAGGCTTAGGCAAGAGA AAAATTAGCCGGGCGTGGCGGCACATGCCTGTGATCCCAGCTACTCAGGAGGCTTAGGCAAGAGA T C SNRNP40 Ensembl:ENSG00000060688 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1164989352 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1173,RMVar_hsa_circ_77241,RMVar_hsa_circ_38215,RMVar_hsa_circ_79760,RMVar_hsa_circ_131047,RMVar_hsa_circ_304438,RMVar_hsa_circ_50169,RMVar_hsa_circ_8040,RMVar_hsa_circ_131048,RMVar_hsa_circ_131049 30893 RMVar_ID_30893 Human_SNP_ID_8245463 A-to-I Human chr1 - 31276853 31276853 31276853 ATATTTTGTATTTTTAGTAGAGACATGGTTTCACCATGTTGACCAGACTGTTCTAGAACTCCTGA ATATTTTGTATTTTTAGTAGAGACATGGTTTCCCCATGTTGACCAGACTGTTCTAGAACTCCTGA T G SNRNP40 Ensembl:ENSG00000060688 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1484168368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10931599 RMVar_hsa_circ_1173,RMVar_hsa_circ_79760,RMVar_hsa_circ_50169,RMVar_hsa_circ_37953,RMVar_hsa_circ_131049,RMVar_hsa_circ_305098,RMVar_hsa_circ_310173,RMVar_hsa_circ_131050,RMVar_hsa_circ_131051,RMVar_hsa_circ_131052,RMVar_hsa_circ_313377,RMVar_hsa_circ_346033,RMVar_hsa_circ_53370,RMVar_hsa_circ_287591 30894 RMVar_ID_30894 Human_SNP_ID_8245944 A-to-I Human chr1 - 31278925 31278925 31278925 CCTATCCATCTGGTAGTTTCTTCTCCTTCTCTACATACCATTATGAGCTACTCTGTCTGTGGAGT CCTATCCATCTGGTAGTTTCTTCTCCTTCTCTGCATACCATTATGAGCTACTCTGTCTGTGGAGT T C SNRNP40 Ensembl:ENSG00000060688 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11583123 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1173,RMVar_hsa_circ_79760,RMVar_hsa_circ_50169,RMVar_hsa_circ_37953,RMVar_hsa_circ_131049,RMVar_hsa_circ_305098,RMVar_hsa_circ_310173,RMVar_hsa_circ_131050,RMVar_hsa_circ_131051,RMVar_hsa_circ_131052,RMVar_hsa_circ_313377,RMVar_hsa_circ_346033,RMVar_hsa_circ_53370,RMVar_hsa_circ_287591 30895 RMVar_ID_30895 Human_SNP_ID_8247077 A-to-I Human chr1 - 31282849 31282849 31282849 CAACGTGGCGAAACCCTGTCTCTACTAAAAATACAAAAATTAGCTGGGCATAGTGGCACACGCCT CAACGTGGCGAAACCCTGTCTCTACTAAAAATGCAAAAATTAGCTGGGCATAGTGGCACACGCCT T C SNRNP40 Ensembl:ENSG00000060688 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1050772323 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 30896 RMVar_ID_30896 Human_SNP_ID_8247389 A-to-I Human chr1 - 31284101 31284101 31284101 CTCCCATCTCAGCCTCCCAAGTAGCTGGGACTATAGGCATATACCACCACACCCAACTTTTTGTT CTCCCATCTCAGCCTCCCAAGTAGCTGGGACTGTAGGCATATACCACCACACCCAACTTTTTGTT T C SNRNP40 Ensembl:ENSG00000060688 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1215378009 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 30897 RMVar_ID_30897 Human_SNP_ID_8247741 A-to-I Human chr1 - 31285285 31285285 31285285 GAGCGGAGATCACGCCACTGCACTCCAGAATGAGCAACAGACAGAGTGAGACTCCCATCTCAAAA GAGCGGAGATCACGCCACTGCACTCCAGAATGTGCAACAGACAGAGTGAGACTCCCATCTCAAAA T A SNRNP40 Ensembl:ENSG00000060688 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4949375 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 30898 RMVar_ID_30898 Human_SNP_ID_8247742 A-to-I Human chr1 - 31285285 31285285 31285285 GAGCGGAGATCACGCCACTGCACTCCAGAATGAGCAACAGACAGAGTGAGACTCCCATCTCAAAA GAGCGGAGATCACGCCACTGCACTCCAGAATGGGCAACAGACAGAGTGAGACTCCCATCTCAAAA T C SNRNP40 Ensembl:ENSG00000060688 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4949375 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 30899 RMVar_ID_30899 Human_SNP_ID_8248202 A-to-I Human chr1 - 31287327 31287327 31287327 ACCTTATTACTCAAGTTAATACTTTTTTTAATAAGCAGTATGTCACATCACCTAAAGATGACTGC ACCTTATTACTCAAGTTAATACTTTTTTTAATTAGCAGTATGTCACATCACCTAAAGATGACTGC T A SNRNP40 Ensembl:ENSG00000060688 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6425732 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2142864,Human_RBP_ID_10931851 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 30900 RMVar_ID_30900 Human_SNP_ID_8248203 A-to-I Human chr1 - 31287327 31287327 31287327 ACCTTATTACTCAAGTTAATACTTTTTTTAATAAGCAGTATGTCACATCACCTAAAGATGACTGC ACCTTATTACTCAAGTTAATACTTTTTTTAATGAGCAGTATGTCACATCACCTAAAGATGACTGC T C SNRNP40 Ensembl:ENSG00000060688 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6425732 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2142864,Human_RBP_ID_10931851 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 30901 RMVar_ID_30901 Human_SNP_ID_8248293 A-to-I Human chr1 - 31287756 31287756 31287756 TGACCTTGTGATCCGCCCCCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCACAC TGACCTTGTGATCCGCCCCCCTCGGCCTCCCAGAGTGCTGGGATTACAGGCGTGAGCCACCACAC T C SNRNP40 Ensembl:ENSG00000060688 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1210828258 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 30902 RMVar_ID_30902 Human_SNP_ID_8248945 A-to-I Human chr1 - 31290041 31290041 31290041 CCTGGGCAACATAGTGAGACCTTGCCTCTACAAATGATTTTTAAAAATTAACTGAGCATGGTGGC CCTGGGCAACATAGTGAGACCTTGCCTCTACAGATGATTTTTAAAAATTAACTGAGCATGGTGGC T C SNRNP40 Ensembl:ENSG00000060688 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1322685921 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79760,RMVar_hsa_circ_50169,RMVar_hsa_circ_131049,RMVar_hsa_circ_310173,RMVar_hsa_circ_131051,RMVar_hsa_circ_131052,RMVar_hsa_circ_313377,RMVar_hsa_circ_287591,RMVar_hsa_circ_131053,RMVar_hsa_circ_28023,RMVar_hsa_circ_334221,RMVar_hsa_circ_338815 30903 RMVar_ID_30903 Human_SNP_ID_8248962 A-to-I Human chr1 - 31290118 31290118 31290118 GTGGTTGCTTACGCCTATAACCCTAGCACTGTAGGAGGCTGAGGCAGGAAGATTGCTTGAGCCCA GTGGTTGCTTACGCCTATAACCCTAGCACTGTGGGAGGCTGAGGCAGGAAGATTGCTTGAGCCCA T C SNRNP40 Ensembl:ENSG00000060688 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1182260987 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10931947 RMVar_hsa_circ_79760,RMVar_hsa_circ_50169,RMVar_hsa_circ_131049,RMVar_hsa_circ_310173,RMVar_hsa_circ_131051,RMVar_hsa_circ_131052,RMVar_hsa_circ_313377,RMVar_hsa_circ_287591,RMVar_hsa_circ_131053,RMVar_hsa_circ_28023,RMVar_hsa_circ_334221,RMVar_hsa_circ_338815 30904 RMVar_ID_30904 Human_SNP_ID_8249004 A-to-I Human chr1 - 31290308 31290308 31290308 TTAGAAAGCTGGGCCTGGTGGCATGTGCTTATAATCCCAGCTATTTGGGAGGCTGAGGCAGGAGG TTAGAAAGCTGGGCCTGGTGGCATGTGCTTATGATCCCAGCTATTTGGGAGGCTGAGGCAGGAGG T C SNRNP40 Ensembl:ENSG00000060688 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1309151763 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79760,RMVar_hsa_circ_50169,RMVar_hsa_circ_131049,RMVar_hsa_circ_310173,RMVar_hsa_circ_131051,RMVar_hsa_circ_131052,RMVar_hsa_circ_313377,RMVar_hsa_circ_287591,RMVar_hsa_circ_131053,RMVar_hsa_circ_28023,RMVar_hsa_circ_334221,RMVar_hsa_circ_338815 30905 RMVar_ID_30905 Human_SNP_ID_8249007 A-to-I Human chr1 - 31290318 31290318 31290318 AAATAAAGCATTAGAAAGCTGGGCCTGGTGGCATGTGCTTATAATCCCAGCTATTTGGGAGGCTG AAATAAAGCATTAGAAAGCTGGGCCTGGTGGCGTGTGCTTATAATCCCAGCTATTTGGGAGGCTG T C SNRNP40 Ensembl:ENSG00000060688 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1019995693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5809564,Human_RBP_ID_10931955 RMVar_hsa_circ_79760,RMVar_hsa_circ_50169,RMVar_hsa_circ_131049,RMVar_hsa_circ_310173,RMVar_hsa_circ_131051,RMVar_hsa_circ_131052,RMVar_hsa_circ_313377,RMVar_hsa_circ_287591,RMVar_hsa_circ_131053,RMVar_hsa_circ_28023,RMVar_hsa_circ_334221,RMVar_hsa_circ_338815 30906 RMVar_ID_30906 Human_SNP_ID_8249964 A-to-I Human chr1 - 31293846 31293846 31293846 ATGAGCCAGGCCAAATGTGGTGGCTCATTCCTATAATCTTAGTGCTTTGGGAGGCCAAGGAGGGA ATGAGCCAGGCCAAATGTGGTGGCTCATTCCTGTAATCTTAGTGCTTTGGGAGGCCAAGGAGGGA T C SNRNP40 Ensembl:ENSG00000060688 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs779048413 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_131054,RMVar_hsa_circ_116377 30907 RMVar_ID_30907 Human_SNP_ID_8251684 A-to-I Human chr1 + 31300249 31300249 31300249 GCCTGGCTAATTGTTGTATTTTTTATAGAGATAAGGTCTTGCCATGTTGTCCAGGCTGGTCTCAA GCCTGGCTAATTGTTGTATTTTTTATAGAGATGAGGTCTTGCCATGTTGTCCAGGCTGGTCTCAA A G ZCCHC17 Ensembl:ENSG00000121766 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1016579604 Functional Loss SNV dbSNP153 33..33 33 - - - 30908 RMVar_ID_30908 Human_SNP_ID_8263523 A-to-I Human chr1 + 31351557 31351557 31351557 AAGTCCAGGAGTTTGAGACCAACCTAAGCAACATAGGGAGACCCTGTCTCTATAAAACATAGAGA AAGTCCAGGAGTTTGAGACCAACCTAAGCAACGTAGGGAGACCCTGTCTCTATAAAACATAGAGA A G ZCCHC17 Ensembl:ENSG00000121766 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1199774141 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107566,RMVar_hsa_circ_131065 30909 RMVar_ID_30909 Human_SNP_ID_8282023 A-to-I Human chr1 + 31429510 31429510 31429510 GGTGGGATGCCCCGAGCATTGTGGGCCTCATCATCTTCCTCCTGTGCACCCTCTTCATCAGGTAT GGTGGGATGCCCCGAGCATTGTGGGCCTCATCGTCTTCCTCCTGTGCACCCTCTTCATCAGGTAT A G SERINC2 Ensembl:ENSG00000168528 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs144747208 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27397514 Human_Splice_Rec_40617,Human_Splice_Rec_40635,Human_Splice_Rec_40661,Human_Splice_Rec_40681,Human_Splice_Rec_40699 Human_miRNA_ID_3076179,Human_miRNA_ID_3076180,Human_miRNA_ID_3076181,Human_miRNA_ID_3076182 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_131077,RMVar_hsa_circ_122052,RMVar_hsa_circ_117413,RMVar_hsa_circ_131079,RMVar_hsa_circ_335345,RMVar_hsa_circ_43299,RMVar_hsa_circ_94979,RMVar_hsa_circ_126817,RMVar_hsa_circ_131080,RMVar_hsa_circ_131081,RMVar_hsa_circ_284457,RMVar_hsa_circ_131082,RMVar_hsa_circ_131083 30910 RMVar_ID_30910 Human_SNP_ID_8335659 A-to-I Human chr1 - 31636367 31636367 31636367 GGCTCAGGTGATCCTCCCACCTTAGCCTCCTGAGTCATTGGGACTATAGGTGTGCGCCACCACAC GGCTCAGGTGATCCTCCCACCTTAGCCTCCTGTGTCATTGGGACTATAGGTGTGCGCCACCACAC T A PEF1 Ensembl:ENSG00000162517 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs541902562 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10934144 RMVar_hsa_circ_131098,RMVar_hsa_circ_83660 30911 RMVar_ID_30911 Human_SNP_ID_8404028 A-to-I Human chr1 - 31908235 31908232 31908236 TGGGCACTTTTAGATAAAAAAAAAAAAAAAACAAAAAACAACACCAAAAAAACAGCAGTGATATA TGGGCACTTTTAGATAAAAAAAAAAAAAAAA____AAACAACACCAAAAAAACAGCAGTGATATA TTTTG T AL136115.2,PTP4A2 Ensembl:ENSG00000269967,Ensembl:ENSG00000184007 lincRNA,Protein coding intron,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1253127374 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_352097,Human_RBP_ID_10935336,Human_RBP_ID_18174795,Human_RBP_ID_23387585 RMVar_hsa_circ_92456,RMVar_hsa_circ_112601,RMVar_hsa_circ_122320,RMVar_hsa_circ_103168,RMVar_hsa_circ_131129,RMVar_hsa_circ_131131,RMVar_hsa_circ_131132,RMVar_hsa_circ_131130,RMVar_hsa_circ_131133 30912 RMVar_ID_30912 Human_SNP_ID_8404030 A-to-I Human chr1 - 31908235 31908234 31908236 TGGGCACTTTTAGATAAAAAAAAAAAAAAAACAAAAAACAACACCAAAAAAACAGCAGTGATATA TGGGCACTTTTAGATAAAAAAAAAAAAAAAA__AAAAACAACACCAAAAAAACAGCAGTGATATA TTG T AL136115.2,PTP4A2 Ensembl:ENSG00000269967,Ensembl:ENSG00000184007 lincRNA,Protein coding intron,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1209502080 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_352097,Human_RBP_ID_10935336,Human_RBP_ID_18174795,Human_RBP_ID_23387585 RMVar_hsa_circ_92456,RMVar_hsa_circ_112601,RMVar_hsa_circ_122320,RMVar_hsa_circ_103168,RMVar_hsa_circ_131129,RMVar_hsa_circ_131131,RMVar_hsa_circ_131132,RMVar_hsa_circ_131130,RMVar_hsa_circ_131133 30913 RMVar_ID_30913 Human_SNP_ID_8406979 A-to-I Human chr1 - 31919970 31919970 31919970 AGGCATGCACCACCACACCTGGCTAATTGTGTATTTTTAGTAGCGACGGGGTTTCTCCATGTTGA AGGCATGCACCACCACACCTGGCTAATTGTGTGTTTTTAGTAGCGACGGGGTTTCTCCATGTTGA T C AL136115.2,PTP4A2 Ensembl:ENSG00000269967,Ensembl:ENSG00000184007 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs148896725 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84392,RMVar_hsa_circ_103168,RMVar_hsa_circ_131132,RMVar_hsa_circ_131134 30914 RMVar_ID_30914 Human_SNP_ID_8407235 A-to-I Human chr1 - 31920783 31920783 31920783 CTGTAATCCCAGCACTTTGGGAGGCCTAGGCAAGCGAATCACCTGAGGTCAGGAGTTCGAGATGA CTGTAATCCCAGCACTTTGGGAGGCCTAGGCAGGCGAATCACCTGAGGTCAGGAGTTCGAGATGA T C AL136115.2,PTP4A2 Ensembl:ENSG00000269967,Ensembl:ENSG00000184007 lincRNA,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1197492569 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84392,RMVar_hsa_circ_103168,RMVar_hsa_circ_131132,RMVar_hsa_circ_131134 30915 RMVar_ID_30915 Human_SNP_ID_8407244 A-to-I Human chr1 - 31920827 31920827 31920827 TGAAGTTTATGAAGAGTTCATGGGCCAGGCGCAGTAGTTCACGCCTGTAATCCCAGCACTTTGGG TGAAGTTTATGAAGAGTTCATGGGCCAGGCGCTGTAGTTCACGCCTGTAATCCCAGCACTTTGGG T A AL136115.2,PTP4A2 Ensembl:ENSG00000269967,Ensembl:ENSG00000184007 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1032228523 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10935741 RMVar_hsa_circ_84392,RMVar_hsa_circ_103168,RMVar_hsa_circ_131132,RMVar_hsa_circ_131134 30916 RMVar_ID_30916 Human_SNP_ID_8407245 A-to-I Human chr1 - 31920827 31920827 31920827 TGAAGTTTATGAAGAGTTCATGGGCCAGGCGCAGTAGTTCACGCCTGTAATCCCAGCACTTTGGG TGAAGTTTATGAAGAGTTCATGGGCCAGGCGCGGTAGTTCACGCCTGTAATCCCAGCACTTTGGG T C AL136115.2,PTP4A2 Ensembl:ENSG00000269967,Ensembl:ENSG00000184007 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1032228523 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10935741 RMVar_hsa_circ_84392,RMVar_hsa_circ_103168,RMVar_hsa_circ_131132,RMVar_hsa_circ_131134 30917 RMVar_ID_30917 Human_SNP_ID_8407619 A-to-I Human chr1 - 31922301 31922301 31922301 TTTTGTATTTTTAGTAGAGATGGGGTTTCTCCATGTTGATCAGGCTGGTCTTGAACTCCTGACCT TTTTGTATTTTTAGTAGAGATGGGGTTTCTCCGTGTTGATCAGGCTGGTCTTGAACTCCTGACCT T C PTP4A2 Ensembl:ENSG00000184007 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1303349592 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84392,RMVar_hsa_circ_103168,RMVar_hsa_circ_131132,RMVar_hsa_circ_131134 30918 RMVar_ID_30918 Human_SNP_ID_8407625 A-to-I Human chr1 - 31922321 31922321 31922321 GTGCCACCACGCCCAACTAATTTTGTATTTTTAGTAGAGATGGGGTTTCTCCATGTTGATCAGGC GTGCCACCACGCCCAACTAATTTTGTATTTTTGGTAGAGATGGGGTTTCTCCATGTTGATCAGGC T C PTP4A2 Ensembl:ENSG00000184007 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs649738 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84392,RMVar_hsa_circ_103168,RMVar_hsa_circ_131132,RMVar_hsa_circ_131134 30919 RMVar_ID_30919 Human_SNP_ID_8410656 A-to-I Human chr1 - 31933177 31933177 31933177 TGGGCAACATAGAGACAACATCTCTACAAAAAATACAAAAACTAGCCAGGCATAGTGGTATGAAC TGGGCAACATAGAGACAACATCTCTACAAAAAGTACAAAAACTAGCCAGGCATAGTGGTATGAAC T C PTP4A2 Ensembl:ENSG00000184007 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs375648361 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84392,RMVar_hsa_circ_103168,RMVar_hsa_circ_131132,RMVar_hsa_circ_131134 30920 RMVar_ID_30920 Human_SNP_ID_8410657 A-to-I Human chr1 - 31933181 31933181 31933181 AGCCTGGGCAACATAGAGACAACATCTCTACAAAAAATACAAAAACTAGCCAGGCATAGTGGTAT AGCCTGGGCAACATAGAGACAACATCTCTACAGAAAATACAAAAACTAGCCAGGCATAGTGGTAT T C PTP4A2 Ensembl:ENSG00000184007 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs981419686 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84392,RMVar_hsa_circ_103168,RMVar_hsa_circ_131132,RMVar_hsa_circ_131134 30921 RMVar_ID_30921 Human_SNP_ID_8411414 A-to-I Human chr1 - 31936317 31936317 31936317 TTCCCGCCTCAGCCTCCCAAGTAGCTGAGAATACAAGTGTGTGCCACCACACCCGGCTAATTTTC TTCCCGCCTCAGCCTCCCAAGTAGCTGAGAATGCAAGTGTGTGCCACCACACCCGGCTAATTTTC T C PTP4A2 Ensembl:ENSG00000184007 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1193543477 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84392,RMVar_hsa_circ_103168,RMVar_hsa_circ_131132,RMVar_hsa_circ_131134 30922 RMVar_ID_30922 Human_SNP_ID_8432302 A-to-I Human chr1 + 32018410 32018410 32018410 TTGAACTCAGGAGACGGAGGTTGCAGTGAGCCAAGATCGCACCACTGCACTCCAGCCTGGGCGAC TTGAACTCAGGAGACGGAGGTTGCAGTGAGCCGAGATCGCACCACTGCACTCCAGCCTGGGCGAC A G KHDRBS1 Ensembl:ENSG00000121774 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1252847799 Functional Loss SNV dbSNP153 33..33 33 - - - 30923 RMVar_ID_30923 Human_SNP_ID_8432507 A-to-I Human chr1 + 32018988 32018988 32018988 AGCTACTCGGGAGCCTGTAATTCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCCA AGCTACTCGGGAGCCTGTAATTCCAGCTACTCCGGAGGCTGAGGCAGGAGAATCACTTGAACCCA A C KHDRBS1 Ensembl:ENSG00000121774 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1236780342 Functional Loss SNV dbSNP153 33..33 33 - - - 30924 RMVar_ID_30924 Human_SNP_ID_8432532 A-to-I Human chr1 + 32019063 32019063 32019063 TTTGCAGTGAGCCGAGATTGCGCCGCCACTGCACTCCAGCCTGGGCGACAGAGCGAGACTCTGTC TTTGCAGTGAGCCGAGATTGCGCCGCCACTGCCCTCCAGCCTGGGCGACAGAGCGAGACTCTGTC A C KHDRBS1 Ensembl:ENSG00000121774 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1299638892 Functional Loss SNV dbSNP153 33..33 33 - - - 30925 RMVar_ID_30925 Human_SNP_ID_8433407 A-to-I Human chr1 + 32022213 32022213 32022213 GGGTTTCACCATAGTAGAAACAGGGTTTCACCATGTTGGCCAGGATAGTCTCGATCTCCTGCCCA GGGTTTCACCATAGTAGAAACAGGGTTTCACCGTGTTGGCCAGGATAGTCTCGATCTCCTGCCCA A G KHDRBS1 Ensembl:ENSG00000121774 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs561792200 Functional Loss SNV dbSNP153 33..33 33 - - - 30926 RMVar_ID_30926 Human_SNP_ID_8433564 A-to-I Human chr1 + 32022766 32022766 32022766 CAAAAATTAGCCAGGTGTGGTGGCATGCGCCTATAGTCACCAGCTACTCGGGAGGCTGAGACAGG CAAAAATTAGCCAGGTGTGGTGGCATGCGCCTGTAGTCACCAGCTACTCGGGAGGCTGAGACAGG A G KHDRBS1 Ensembl:ENSG00000121774 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs115097716 Functional Loss SNV dbSNP153 33..33 33 - - - 30927 RMVar_ID_30927 Human_SNP_ID_8434005 A-to-I Human chr1 + 32024327 32024327 32024327 GGTTTTCTAAAATTTTTTATTAATTTTTTTTTAGAGACAGGGTCTTGTTCTGTCACCCAAGCTGG GGTTTTCTAAAATTTTTTATTAATTTTTTTTTGGAGACAGGGTCTTGTTCTGTCACCCAAGCTGG A G KHDRBS1 Ensembl:ENSG00000121774 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs572582207 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5810546,Human_RBP_ID_10936670,Human_RBP_ID_17557090,Human_RBP_ID_24684099 30928 RMVar_ID_30928 Human_SNP_ID_8434039 A-to-I Human chr1 + 32024440 32024440 32024440 TCAAGTGATCGTCCTGCCTCAGCCTCTCTAGTAACTGGGACAACAGTTGTACGCCACCACACTGA TCAAGTGATCGTCCTGCCTCAGCCTCTCTAGTGACTGGGACAACAGTTGTACGCCACCACACTGA A G KHDRBS1 Ensembl:ENSG00000121774 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1334711201 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10936671 30929 RMVar_ID_30929 Human_SNP_ID_8434215 A-to-I Human chr1 + 32024996 32024996 32024996 AAAACAAACAAAAAAAAAGGCGGGGGGAGCATAGTAGGTCACGCCTATAATCCCAGCACTTTGGG AAAACAAACAAAAAAAAAGGCGGGGGGAGCATGGTAGGTCACGCCTATAATCCCAGCACTTTGGG A G KHDRBS1 Ensembl:ENSG00000121774 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs888040910 Functional Loss SNV dbSNP153 33..33 33 - - - 30930 RMVar_ID_30930 Human_SNP_ID_8434226 A-to-I Human chr1 + 32025035 32025035 32025035 CACGCCTATAATCCCAGCACTTTGGGAGGCCGAAGTGGAAGGATCATTTGAGCCCAGGAGTTCAA CACGCCTATAATCCCAGCACTTTGGGAGGCCGCAGTGGAAGGATCATTTGAGCCCAGGAGTTCAA A C KHDRBS1 Ensembl:ENSG00000121774 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1211618754 Functional Loss SNV dbSNP153 33..33 33 - - - 30931 RMVar_ID_30931 Human_SNP_ID_8434278 A-to-I Human chr1 + 32025186 32025186 32025186 TACTGGGGGTGCTGAGGTGGGAGGATCGCCTGAACCCAGGAGGTTGAGGCTACAGTGAGCCATTA TACTGGGGGTGCTGAGGTGGGAGGATCGCCTGTACCCAGGAGGTTGAGGCTACAGTGAGCCATTA A T KHDRBS1 Ensembl:ENSG00000121774 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs997038206 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17558347 30932 RMVar_ID_30932 Human_SNP_ID_8434701 A-to-I Human chr1 + 32026432 32026432 32026432 CTTCTGCCTCAGCTTCCCCAAATGCTGAGATTACAAGTGTGAGCCACCATGCCTGGCCACTGCTA CTTCTGCCTCAGCTTCCCCAAATGCTGAGATTCCAAGTGTGAGCCACCATGCCTGGCCACTGCTA A C KHDRBS1 Ensembl:ENSG00000121774 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs143773992 Functional Loss SNV dbSNP153 33..33 33 - - - 30933 RMVar_ID_30933 Human_SNP_ID_8435700 A-to-I Human chr1 + 32030326 32030326 32030326 TCAGAAATTGAGAAGATTCAGAAAGGAGACTCAAAAAAGGATGATGAGGAGAATTACTTGGATTT TCAGAAATTGAGAAGATTCAGAAAGGAGACTCGAAAAAGGATGATGAGGAGAATTACTTGGATTT A G KHDRBS1 Ensembl:ENSG00000121774 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs375755192 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19091,Human_RBP_ID_352160,Human_RBP_ID_977598,Human_RBP_ID_1154061,Human_RBP_ID_1429112,Human_RBP_ID_1745371,Human_RBP_ID_4044719,Human_RBP_ID_8308181,Human_RBP_ID_10936776,Human_RBP_ID_17452349,Human_RBP_ID_17679125,Human_RBP_ID_17748673,Human_RBP_ID_18571951,Human_RBP_ID_23387753,Human_RBP_ID_26862140 Human_Splice_Rec_42470,Human_Splice_Rec_42471,Human_Splice_Rec_42486,Human_Splice_Rec_42487,Human_Splice_Rec_42502,Human_Splice_Rec_42503,Human_Splice_Rec_42516,Human_Splice_Rec_42517 RMVar_hsa_circ_131144,RMVar_hsa_circ_300160,RMVar_hsa_circ_311133,RMVar_hsa_circ_324915,RMVar_hsa_circ_341253,RMVar_hsa_circ_309730,RMVar_hsa_circ_275865,RMVar_hsa_circ_279356,RMVar_hsa_circ_131145,RMVar_hsa_circ_131142,RMVar_hsa_circ_131143 30934 RMVar_ID_30934 Human_SNP_ID_8440101 A-to-I Human chr1 + 32048252 32048252 32048252 TTTCTTGGCTGCGCATGGCAGCTCATGCCTGTAATCCCAACACCTGGGGAGGCTGAGTTGGGAGG TTTCTTGGCTGCGCATGGCAGCTCATGCCTGTGATCCCAACACCTGGGGAGGCTGAGTTGGGAGG A G KHDRBS1 Ensembl:ENSG00000121774 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1304097699 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125672,RMVar_hsa_circ_131156 30935 RMVar_ID_30935 Human_SNP_ID_8440112 A-to-I Human chr1 + 32048298 32048298 32048298 GGGAGGCTGAGTTGGGAGGATCACTTGAGGCCAGGAGTTCAAGACAAGCCGGGACAACATAGCAG GGGAGGCTGAGTTGGGAGGATCACTTGAGGCCGGGAGTTCAAGACAAGCCGGGACAACATAGCAG A G KHDRBS1 Ensembl:ENSG00000121774 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs944177321 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125672,RMVar_hsa_circ_131156 30936 RMVar_ID_30936 Human_SNP_ID_8442244 A-to-I Human chr1 + 32057187 32057181 32057187 TTGAAGCCGAGGTACGAATCTGGACCTTTTTTATTTTTATTTTTGAGACAGGGTCTTGTTCTGTC TTGAAGCCGAGGTACGAATCTGGACCT______TTTTTATTTTTGAGACAGGGTCTTGTTCTGTC TTTTTTA T KHDRBS1 Ensembl:ENSG00000121774 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1260940204 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_10937787 RMVar_hsa_circ_125672,RMVar_hsa_circ_131156 30937 RMVar_ID_30937 Human_SNP_ID_8442551 A-to-I Human chr1 + 32058200 32058199 32058200 GCTTCTACCTCCTGGGCTCAAGACATCCTCTCACCTCAGCCTCCAGAGTAGCTGGGACTGTAGGC GCTTCTACCTCCTGGGCTCAAGACATCCTCTC_CCTCAGCCTCCAGAGTAGCTGGGACTGTAGGC CA C KHDRBS1 Ensembl:ENSG00000121774 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1437926150 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_125672,RMVar_hsa_circ_131156 30938 RMVar_ID_30938 Human_SNP_ID_8447867 A-to-I Human chr1 + 32078362 32078362 32078362 AAAACTAGCCAGGTGTGGTGAGGCACGCCTATAGTCCCAGCTACTCAGGAAGCTGAGGTGGGAGA AAAACTAGCCAGGTGTGGTGAGGCACGCCTATTGTCCCAGCTACTCAGGAAGCTGAGGTGGGAGA A T TMEM39B Ensembl:ENSG00000121775 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs920399499 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22153,RMVar_hsa_circ_131158,RMVar_hsa_circ_310499,RMVar_hsa_circ_339170 30939 RMVar_ID_30939 Human_SNP_ID_8449670 A-to-I Human chr1 + 32084639 32084639 32084639 TCGCCCAGGGTGGAGTGCAATGACACGATCTCAGCTCACTGCAACCTCCGCCTCCCGAGTTCAAG TCGCCCAGGGTGGAGTGCAATGACACGATCTCGGCTCACTGCAACCTCCGCCTCCCGAGTTCAAG A G TMEM39B Ensembl:ENSG00000121775 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1436163687 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22153,RMVar_hsa_circ_131158,RMVar_hsa_circ_310499,RMVar_hsa_circ_339170 30940 RMVar_ID_30940 Human_SNP_ID_8457400 A-to-I Human chr1 + 32113133 32113133 32113133 TCTAAATCTGCCGGTCTTGGTGGCTCACGCCTATGATGCCAGCACTTTGAGAGGATGAGGTGGGA TCTAAATCTGCCGGTCTTGGTGGCTCACGCCTGTGATGCCAGCACTTTGAGAGGATGAGGTGGGA A G KPNA6 Ensembl:ENSG00000025800 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs999210188 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94894,RMVar_hsa_circ_131161 30941 RMVar_ID_30941 Human_SNP_ID_8460841 A-to-I Human chr1 + 32124945 32124945 32124945 CAGCTCACTGCAACCTCCACCTCCCAGGTTCAAACAATTCTCCTGCCTCAGCCTCCTGAGTAGCC CAGCTCACTGCAACCTCCACCTCCCAGGTTCAGACAATTCTCCTGCCTCAGCCTCCTGAGTAGCC A G KPNA6 Ensembl:ENSG00000025800 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1215474680 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94894,RMVar_hsa_circ_131161 30942 RMVar_ID_30942 Human_SNP_ID_8460842 A-to-I Human chr1 + 32124948 32124948 32124948 CTCACTGCAACCTCCACCTCCCAGGTTCAAACAATTCTCCTGCCTCAGCCTCCTGAGTAGCCGGG CTCACTGCAACCTCCACCTCCCAGGTTCAAACGATTCTCCTGCCTCAGCCTCCTGAGTAGCCGGG A G KPNA6 Ensembl:ENSG00000025800 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs898873005 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94894,RMVar_hsa_circ_131161 30943 RMVar_ID_30943 Human_SNP_ID_8462130 A-to-I Human chr1 + 32129595 32129595 32129595 GTTTTTATTTGGAGACAGGGTCTCGCTCTGTCACCCAGGCTGGAGTGCAGTAGCGCCATCATAGC GTTTTTATTTGGAGACAGGGTCTCGCTCTGTCCCCCAGGCTGGAGTGCAGTAGCGCCATCATAGC A C KPNA6 Ensembl:ENSG00000025800 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1478396808 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94894,RMVar_hsa_circ_131161 30944 RMVar_ID_30944 Human_SNP_ID_8462131 A-to-I Human chr1 + 32129595 32129595 32129595 GTTTTTATTTGGAGACAGGGTCTCGCTCTGTCACCCAGGCTGGAGTGCAGTAGCGCCATCATAGC GTTTTTATTTGGAGACAGGGTCTCGCTCTGTCTCCCAGGCTGGAGTGCAGTAGCGCCATCATAGC A T KPNA6 Ensembl:ENSG00000025800 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1478396808 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94894,RMVar_hsa_circ_131161 30945 RMVar_ID_30945 Human_SNP_ID_8465687 A-to-I Human chr1 + 32143300 32143300 32143300 ATTGCTCAGGCTGCTCTTGAACTCCTGGGCTCAAGCAGTCTGCCCACTTTGGCCTCCCAAAGTGC ATTGCTCAGGCTGCTCTTGAACTCCTGGGCTCGAGCAGTCTGCCCACTTTGGCCTCCCAAAGTGC A G KPNA6 Ensembl:ENSG00000025800 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1172267052 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557096 RMVar_hsa_circ_94894,RMVar_hsa_circ_131161 30946 RMVar_ID_30946 Human_SNP_ID_8471194 A-to-I Human chr1 + 32164998 32164998 32164998 CGGCTCACTGCAACCTCTGCCTCCTGAGCTCAAAGCAGTCCTTCCACCTCAGCCTCCCAAGTAGC CGGCTCACTGCAACCTCTGCCTCCTGAGCTCAGAGCAGTCCTTCCACCTCAGCCTCCCAAGTAGC A G KPNA6 Ensembl:ENSG00000025800 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1230281910 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37490,RMVar_hsa_circ_368621,RMVar_hsa_circ_43251,RMVar_hsa_circ_105157,RMVar_hsa_circ_131167,RMVar_hsa_circ_359375,RMVar_hsa_circ_131169,RMVar_hsa_circ_103252,RMVar_hsa_circ_320475,RMVar_hsa_circ_44065,RMVar_hsa_circ_279465,RMVar_hsa_circ_131173 30947 RMVar_ID_30947 Human_SNP_ID_8471243 A-to-I Human chr1 + 32165154 32165154 32165154 CTCTTGAACTACTGGGCTTAAGCAATCCTCCCACCTTGGCTTCTCAAAGTGCTGGGATTACAGGC CTCTTGAACTACTGGGCTTAAGCAATCCTCCCTCCTTGGCTTCTCAAAGTGCTGGGATTACAGGC A T KPNA6 Ensembl:ENSG00000025800 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048403405 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10940051 RMVar_hsa_circ_37490,RMVar_hsa_circ_368621,RMVar_hsa_circ_43251,RMVar_hsa_circ_105157,RMVar_hsa_circ_131167,RMVar_hsa_circ_359375,RMVar_hsa_circ_131169,RMVar_hsa_circ_103252,RMVar_hsa_circ_320475,RMVar_hsa_circ_44065,RMVar_hsa_circ_279465,RMVar_hsa_circ_131173 30948 RMVar_ID_30948 Human_SNP_ID_8471964 A-to-I Human chr1 + 32167514 32167514 32167514 TGTGGGAATCTATTCCAGATTCCAGTGACACTATAACAGTTTACCAGTTTTCCCTTCTGGAGAAG TGTGGGAATCTATTCCAGATTCCAGTGACACTGTAACAGTTTACCAGTTTTCCCTTCTGGAGAAG A G KPNA6 Ensembl:ENSG00000025800 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs557063771 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105157,RMVar_hsa_circ_131167,RMVar_hsa_circ_99559,RMVar_hsa_circ_131175 30949 RMVar_ID_30949 Human_SNP_ID_8472191 A-to-I Human chr1 + 32168331 32168331 32168331 TCTGCTTTAGCCTCCTGAGTAGCTGGGGTTACAGGCACGTGCCACCACGCCCGGCTAATTTTTTG TCTGCTTTAGCCTCCTGAGTAGCTGGGGTTACGGGCACGTGCCACCACGCCCGGCTAATTTTTTG A G KPNA6 Ensembl:ENSG00000025800 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1298549857 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105157,RMVar_hsa_circ_131167,RMVar_hsa_circ_99559,RMVar_hsa_circ_131175 30950 RMVar_ID_30950 Human_SNP_ID_8472220 A-to-I Human chr1 + 32168450 32168450 32168450 GATGTCAGATGATCCTCCCACCTTGGCCTCCCAGAGTGCTGGGATTATAGGCATGAGCCACCTGG GATGTCAGATGATCCTCCCACCTTGGCCTCCCGGAGTGCTGGGATTATAGGCATGAGCCACCTGG A G KPNA6 Ensembl:ENSG00000025800 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1002998755 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105157,RMVar_hsa_circ_131167,RMVar_hsa_circ_99559,RMVar_hsa_circ_131175 30951 RMVar_ID_30951 Human_SNP_ID_8475970 A-to-I Human chr1 + 32182806 32182806 32182806 AATCTTAGGGACGACTAGGCAGAGTGGCTCACACCTGTAACTCCAGCACTTTGGGAGGCCAAGGC AATCTTAGGGACGACTAGGCAGAGTGGCTCACTCCTGTAACTCCAGCACTTTGGGAGGCCAAGGC A T TXLNA Ensembl:ENSG00000084652 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1384223715 Functional Loss SNV dbSNP153 33..33 33 - - - 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_131181,RMVar_hsa_circ_131182 30952 RMVar_ID_30952 Human_SNP_ID_8476008 A-to-I Human chr1 + 32182944 32182944 32182944 AAAAAATCAGCCGGGCGTGGTGGCACGTGCCTATAATCCCAGATACTCGGGAGGCTGAGGCAGGA AAAAAATCAGCCGGGCGTGGTGGCACGTGCCTGTAATCCCAGATACTCGGGAGGCTGAGGCAGGA A G TXLNA Ensembl:ENSG00000084652 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1162254143 Functional Loss SNV dbSNP153 33..33 33 - - - 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_131181,RMVar_hsa_circ_131182 30953 RMVar_ID_30953 Human_SNP_ID_8476027 A-to-I Human chr1 + 32183022 32183022 32183022 CCGTGAGGCAGAGTTTTCAGTGAGCTGAGATCATGCCATTGCACTCCAGCCTGGGTGACAGGGTG CCGTGAGGCAGAGTTTTCAGTGAGCTGAGATCGTGCCATTGCACTCCAGCCTGGGTGACAGGGTG A G TXLNA Ensembl:ENSG00000084652 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs973698896 Functional Loss SNV dbSNP153 33..33 33 - - - 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_131181,RMVar_hsa_circ_131182 30954 RMVar_ID_30954 Human_SNP_ID_8476133 A-to-I Human chr1 + 32183331 32183331 32183331 TTTTTTTAGTAGTGACAGGGTTTCACTGTGTTAGCCAGGATAGTCTCGATCTCCTGACCTCATGA TTTTTTTAGTAGTGACAGGGTTTCACTGTGTTGGCCAGGATAGTCTCGATCTCCTGACCTCATGA A G TXLNA Ensembl:ENSG00000084652 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs914745952 Functional Loss SNV dbSNP153 33..33 33 - - - 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_131181,RMVar_hsa_circ_131182 30955 RMVar_ID_30955 Human_SNP_ID_8477520 A-to-I Human chr1 + 32188383 32188383 32188383 AAGCAAGGCTGGGTGTGGTGGCTCACACCTGTAATCCCAACACTTTGGGAGGCTGAGGTGGATGG AAGCAAGGCTGGGTGTGGTGGCTCACACCTGTCATCCCAACACTTTGGGAGGCTGAGGTGGATGG A C TXLNA Ensembl:ENSG00000084652 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1049931301 Functional Loss SNV dbSNP153 33..33 33 - - - 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_39868,RMVar_hsa_circ_131182,RMVar_hsa_circ_301133,RMVar_hsa_circ_131184,RMVar_hsa_circ_277720,RMVar_hsa_circ_131186 30956 RMVar_ID_30956 Human_SNP_ID_8486464 A-to-I Human chr1 - 32219029 32219028 32219029 TGGCTCACTGCAACCTCCGCCTCCCAGGTTCAAGTGACTCTCCTTCCTTAGCCTCCCCACTAGCT TGGCTCACTGCAACCTCCGCCTCCCAGGTTCA_GTGACTCTCCTTCCTTAGCCTCCCCACTAGCT CT C TMEM234 Ensembl:ENSG00000160055 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1225471839 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_16739,RMVar_hsa_circ_87718,RMVar_hsa_circ_131191,RMVar_hsa_circ_102787,RMVar_hsa_circ_131193 30957 RMVar_ID_30957 Human_SNP_ID_8486465 A-to-I Human chr1 - 32219029 32219029 32219029 TGGCTCACTGCAACCTCCGCCTCCCAGGTTCAAGTGACTCTCCTTCCTTAGCCTCCCCACTAGCT TGGCTCACTGCAACCTCCGCCTCCCAGGTTCAGGTGACTCTCCTTCCTTAGCCTCCCCACTAGCT T C TMEM234 Ensembl:ENSG00000160055 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs948616964 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16739,RMVar_hsa_circ_87718,RMVar_hsa_circ_131191,RMVar_hsa_circ_102787,RMVar_hsa_circ_131193 30958 RMVar_ID_30958 Human_SNP_ID_8486612 A-to-I Human chr1 - 32219648 32219648 32219648 CAGCTCTGGGCAGGGCACAGTGGCTCAGGCCTATAATTCCAGCACTTTTGGAGGCTGAGGTGGGC CAGCTCTGGGCAGGGCACAGTGGCTCAGGCCTGTAATTCCAGCACTTTTGGAGGCTGAGGTGGGC T C TMEM234 Ensembl:ENSG00000160055 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1011240034 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_222561 RMVar_hsa_circ_16739,RMVar_hsa_circ_87718,RMVar_hsa_circ_131191,RMVar_hsa_circ_102787,RMVar_hsa_circ_131193 30959 RMVar_ID_30959 Human_SNP_ID_8487587 A-to-I Human chr1 + 32222915 32222915 32222915 GCCCAGGAGTTGGAGACCAGCCTGAGCAACGTAGTAAGACCCATCTCTACACACAAAAAAATTAG GCCCAGGAGTTGGAGACCAGCCTGAGCAACGTGGTAAGACCCATCTCTACACACAAAAAAATTAG A G EIF3I Ensembl:ENSG00000084623 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs774523833 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10941476 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 30960 RMVar_ID_30960 Human_SNP_ID_8488152 A-to-I Human chr1 + 32225014 32225014 32225014 CGCCATCACACCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGAC CGCCATCACACCTGGCTAATTTTTGTATTTTTGGTAGAGACAGGGTTTCACCATGTTGGCCAGAC A G EIF3I Ensembl:ENSG00000084623 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1302773277 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77506,RMVar_hsa_circ_5429,RMVar_hsa_circ_108103,RMVar_hsa_circ_131197,RMVar_hsa_circ_88535,RMVar_hsa_circ_84932,RMVar_hsa_circ_131199,RMVar_hsa_circ_299286,RMVar_hsa_circ_375854,RMVar_hsa_circ_109713,RMVar_hsa_circ_94282,RMVar_hsa_circ_131202,RMVar_hsa_circ_131204,RMVar_hsa_circ_131203,RMVar_hsa_circ_131200,RMVar_hsa_circ_131201,RMVar_hsa_circ_131208,RMVar_hsa_circ_131209 30961 RMVar_ID_30961 Human_SNP_ID_8488157 A-to-I Human chr1 + 32225034 32225034 32225034 TTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGACTGGTCTCAAACTCCAGACCT TTTTGTATTTTTAGTAGAGACAGGGTTTCACCGTGTTGGCCAGACTGGTCTCAAACTCCAGACCT A G EIF3I Ensembl:ENSG00000084623 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs752038947 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77506,RMVar_hsa_circ_5429,RMVar_hsa_circ_108103,RMVar_hsa_circ_131197,RMVar_hsa_circ_88535,RMVar_hsa_circ_84932,RMVar_hsa_circ_131199,RMVar_hsa_circ_299286,RMVar_hsa_circ_375854,RMVar_hsa_circ_109713,RMVar_hsa_circ_94282,RMVar_hsa_circ_131202,RMVar_hsa_circ_131204,RMVar_hsa_circ_131203,RMVar_hsa_circ_131200,RMVar_hsa_circ_131201,RMVar_hsa_circ_131208,RMVar_hsa_circ_131209 30962 RMVar_ID_30962 Human_SNP_ID_8488275 A-to-I Human chr1 + 32225514 32225514 32225514 CCTGTAATCCCAGCACTTTGGGAGGTTGAGGCAGGTGGATCACCTGAGGTCAGGAGTGCAAGACC CCTGTAATCCCAGCACTTTGGGAGGTTGAGGCGGGTGGATCACCTGAGGTCAGGAGTGCAAGACC A G EIF3I Ensembl:ENSG00000084623 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1245828325 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77506,RMVar_hsa_circ_5429,RMVar_hsa_circ_108103,RMVar_hsa_circ_131197,RMVar_hsa_circ_88535,RMVar_hsa_circ_84932,RMVar_hsa_circ_131199,RMVar_hsa_circ_299286,RMVar_hsa_circ_375854,RMVar_hsa_circ_109713,RMVar_hsa_circ_94282,RMVar_hsa_circ_131202,RMVar_hsa_circ_131204,RMVar_hsa_circ_131203,RMVar_hsa_circ_131200,RMVar_hsa_circ_131201,RMVar_hsa_circ_131208,RMVar_hsa_circ_131209 30963 RMVar_ID_30963 Human_SNP_ID_8488658 A-to-I Human chr1 + 32226684 32226684 32226684 CACCTCCCTGGTTCAAGCAATTCCCCTGCCTTAGCCTCCCGAGTAGCTGGGATTACAGGTGCATG CACCTCCCTGGTTCAAGCAATTCCCCTGCCTTGGCCTCCCGAGTAGCTGGGATTACAGGTGCATG A G EIF3I Ensembl:ENSG00000084623 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1032855583 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77506,RMVar_hsa_circ_5429,RMVar_hsa_circ_84932,RMVar_hsa_circ_375854,RMVar_hsa_circ_94282,RMVar_hsa_circ_131202,RMVar_hsa_circ_131200,RMVar_hsa_circ_131201,RMVar_hsa_circ_82219,RMVar_hsa_circ_80192,RMVar_hsa_circ_99378,RMVar_hsa_circ_131208,RMVar_hsa_circ_131209,RMVar_hsa_circ_294150,RMVar_hsa_circ_83976,RMVar_hsa_circ_131212,RMVar_hsa_circ_131213,RMVar_hsa_circ_131214,RMVar_hsa_circ_131211,RMVar_hsa_circ_131215 30964 RMVar_ID_30964 Human_SNP_ID_8489634 A-to-I Human chr1 + 32230249 32230249 32230249 ACTTCTTATCTCAATTTTTCTGCTTTATTATTATTATTTTTTGAGACAGGGTCTCACTCTGTTGC ACTTCTTATCTCAATTTTTCTGCTTTATTATTGTTATTTTTTGAGACAGGGTCTCACTCTGTTGC A G EIF3I Ensembl:ENSG00000084623 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1339693397 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5429,RMVar_hsa_circ_84932,RMVar_hsa_circ_94282,RMVar_hsa_circ_131200,RMVar_hsa_circ_131201,RMVar_hsa_circ_82219,RMVar_hsa_circ_99378,RMVar_hsa_circ_83976,RMVar_hsa_circ_131213,RMVar_hsa_circ_131214,RMVar_hsa_circ_131223,RMVar_hsa_circ_97501,RMVar_hsa_circ_117717,RMVar_hsa_circ_131215,RMVar_hsa_circ_131220,RMVar_hsa_circ_131222,RMVar_hsa_circ_108423 30965 RMVar_ID_30965 Human_SNP_ID_8489683 A-to-I Human chr1 - 32230488 32230488 32230488 CCGAGGCGCAGTGGCTCACGCCTGTAATCCCAACACTTTGGGAGGCCGAGGCGGGTGGATCACTT CCGAGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGTGGATCACTT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1455288533 Functional Loss SNV dbSNP153 33..33 33 - - - 30966 RMVar_ID_30966 Human_SNP_ID_8489707 A-to-I Human chr1 - 32230605 32230605 32230605 TTACGAACTCCTGGCCTCAAGCCGCCTTCCTTAGCCTCCCAATGTGCTGGGATTACAGGCATGAG TTACGAACTCCTGGCCTCAAGCCGCCTTCCTTGGCCTCCCAATGTGCTGGGATTACAGGCATGAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1475583768 Functional Loss SNV dbSNP153 33..33 33 - - - 30967 RMVar_ID_30967 Human_SNP_ID_8489740 A-to-I Human chr1 - 32230741 32230741 32230741 CGGTTCACTGGAACCTCCCCCTCCTGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTGAGTGGTT CGGTTCACTGGAACCTCCCCCTCCTGGGTTCACGCAATTCTCCTGCCTCAGCCTCCTGAGTGGTT T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs865795547 Functional Loss SNV dbSNP153 33..33 33 - - - 30968 RMVar_ID_30968 Human_SNP_ID_8489761 A-to-I Human chr1 - 32230839 32230833 32230839 GAGGTGGCACTCCCCAAATGCAAATTGTTATTATTATTTATTTATTTTGAGATGGAGTCTTACTC GAGGTGGCACTCCCCAAATGCAAATTGTTATT______TATTTATTTTGAGATGGAGTCTTACTC AAATAAT A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1356725152 Functional Loss DEL dbSNP153 33..38 33 - - - 30969 RMVar_ID_30969 Human_SNP_ID_8490471 A-to-I Human chr1 - 32233537 32233537 32233537 GCCTGTAATCCCAGCACTTTGGGAGCTGAGGCAGGCAGGTCACCTGAGATCAGGAGTTTGAGACC GCCTGTAATCCCAGCACTTTGGGAGCTGAGGCGGGCAGGTCACCTGAGATCAGGAGTTTGAGACC T C MTMR9LP Ensembl:ENSG00000220785 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1401720287 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_131225 30970 RMVar_ID_30970 Human_SNP_ID_8490601 A-to-I Human chr1 - 32234093 32234092 32234093 GAGTTTCACCATATTGGCCAGTCTGATCTCAAACTCCTGACCTCAGGTGATCTGCCCACCTCGGC GAGTTTCACCATATTGGCCAGTCTGATCTCAA_CTCCTGACCTCAGGTGATCTGCCCACCTCGGC GT G MTMR9LP Ensembl:ENSG00000220785 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1165814850 Functional Loss DEL dbSNP153 33..33 33 - - - Human_Splice_Rec_43089 RMVar_hsa_circ_131225 30971 RMVar_ID_30971 Human_SNP_ID_8490607 A-to-I Human chr1 - 32234118 32234118 32234118 AATTTTTATACTTTTAGTATAGATGGAGTTTCACCATATTGGCCAGTCTGATCTCAAACTCCTGA AATTTTTATACTTTTAGTATAGATGGAGTTTCCCCATATTGGCCAGTCTGATCTCAAACTCCTGA T G MTMR9LP Ensembl:ENSG00000220785 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1393286523 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17339925 Human_Splice_Rec_43089 RMVar_hsa_circ_131225 30972 RMVar_ID_30972 Human_SNP_ID_8490609 A-to-I Human chr1 - 32234135 32234135 32234135 TGCCACCACGTCCGGCTAATTTTTATACTTTTAGTATAGATGGAGTTTCACCATATTGGCCAGTC TGCCACCACGTCCGGCTAATTTTTATACTTTTGGTATAGATGGAGTTTCACCATATTGGCCAGTC T C MTMR9LP Ensembl:ENSG00000220785 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1419127042 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9552910,Human_RBP_ID_17339925 Human_Splice_Rec_43089 RMVar_hsa_circ_131225 30973 RMVar_ID_30973 Human_SNP_ID_8490622 A-to-I Human chr1 - 32234170 32234170 32234170 CCTCAGCCTCCCGAGTAGCTGGGATTACAGGAATGTGCCACCACGTCCGGCTAATTTTTATACTT CCTCAGCCTCCCGAGTAGCTGGGATTACAGGAGTGTGCCACCACGTCCGGCTAATTTTTATACTT T C MTMR9LP Ensembl:ENSG00000220785 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1046562434 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9552910 RMVar_hsa_circ_131225 30974 RMVar_ID_30974 Human_SNP_ID_8490626 A-to-I Human chr1 - 32234186 32234186 32234186 TCAAGCTATTCTCCAGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGAATGTGCCACCACGTCCG TCAAGCTATTCTCCAGCCTCAGCCTCCCGAGTGGCTGGGATTACAGGAATGTGCCACCACGTCCG T C MTMR9LP Ensembl:ENSG00000220785 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1237316278 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9552910 RMVar_hsa_circ_131225 30975 RMVar_ID_30975 Human_SNP_ID_8491446 A-to-I Human chr1 - 32237774 32237774 32237774 GCAGGCTGAGGAGGGTGGATCCCTTGAGCCCAAGAGTTTGAGACCAGCCTGGGCAACATAGGGAG GCAGGCTGAGGAGGGTGGATCCCTTGAGCCCAGGAGTTTGAGACCAGCCTGGGCAACATAGGGAG T C MTMR9LP Ensembl:ENSG00000220785 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1360320414 Functional Loss SNV dbSNP153 33..33 33 - - - 30976 RMVar_ID_30976 Human_SNP_ID_8493247 A-to-I Human chr1 + 32244776 32244776 32244776 AGAAGCCTTTTTTTAATTTTTTATTTTGAGACAGGTCGGCCTCTGTCACCCAGGCCTGGAGTGTA AGAAGCCTTTTTTTAATTTTTTATTTTGAGACGGGTCGGCCTCTGTCACCCAGGCCTGGAGTGTA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1245414173 Functional Loss SNV dbSNP153 33..33 33 - - - 30977 RMVar_ID_30977 Human_SNP_ID_8493342 A-to-I Human chr1 + 32245076 32245076 32245076 GTGAGCCACCGCGCCCGGCGAGACGGAGTCTCACTCTGTTGCCCAGGCTGGAGTGCAGTGGCGCA GTGAGCCACCGCGCCCGGCGAGACGGAGTCTCGCTCTGTTGCCCAGGCTGGAGTGCAGTGGCGCA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1349100146 Functional Loss SNV dbSNP153 33..33 33 - - - 30978 RMVar_ID_30978 Human_SNP_ID_8502375 A-to-I Human chr1 + 32277918 32277918 32277918 ATGCCTACTTCCAGGTGCTGTGGCTCAAGCCTATAACTCCAGCACTTTGGGAGGCCAAGGTGGGT ATGCCTACTTCCAGGTGCTGTGGCTCAAGCCTGTAACTCCAGCACTTTGGGAGGCCAAGGTGGGT A G LCK Ensembl:ENSG00000182866 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1290378522 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114229,RMVar_hsa_circ_80142,RMVar_hsa_circ_131226,RMVar_hsa_circ_131227 30979 RMVar_ID_30979 Human_SNP_ID_8506490 A-to-I Human chr1 + 32294288 32294288 32294288 CTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCGTGCGCCACCATGCCTGGCTAGTTTTT CTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTCCAGGCGTGCGCCACCATGCCTGGCTAGTTTTT A C HDAC1 Ensembl:ENSG00000116478 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs914974257 Functional Loss SNV dbSNP153 33..33 33 - - - 30980 RMVar_ID_30980 Human_SNP_ID_8506992 A-to-I Human chr1 + 32296579 32296579 32296579 GGTTGTCTTTTGTTTAGAGACAGGATTTCGCCATGTTGCCCAGGCTGGTCTCAAACTCCTGAGCT GGTTGTCTTTTGTTTAGAGACAGGATTTCGCCGTGTTGCCCAGGCTGGTCTCAAACTCCTGAGCT A G HDAC1 Ensembl:ENSG00000116478 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1435190917 Functional Loss SNV dbSNP153 33..33 33 - - - 30981 RMVar_ID_30981 Human_SNP_ID_8508931 A-to-I Human chr1 + 32304825 32304825 32304825 GCTCAAAGCAATCCGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCATAC GCTCAAAGCAATCCGCCTGCCTCGGCCTCCCAGAGTGCTGGGATTACAGGCATGAGCCACCATAC A G HDAC1 Ensembl:ENSG00000116478 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs966718921 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_341211 30982 RMVar_ID_30982 Human_SNP_ID_8509842 A-to-I Human chr1 + 32309092 32309092 32309092 CCTTAGCCTCCCAAAGCGTTAGGATTATAGGCATGAGCCACCACGCCCAGCCAAGAGTTCATTTG CCTTAGCCTCCCAAAGCGTTAGGATTATAGGCGTGAGCCACCACGCCCAGCCAAGAGTTCATTTG A G HDAC1 Ensembl:ENSG00000116478 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs770920857 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_341211 30983 RMVar_ID_30983 Human_SNP_ID_8510366 A-to-I Human chr1 + 32311347 32311347 32311347 AAAATTAGCCGGGCGTGGTCGCGGGTGCCTGTAATCCCAGCTACTCAGGAGTCTGAGACGGGAGA AAAATTAGCCGGGCGTGGTCGCGGGTGCCTGTGATCCCAGCTACTCAGGAGTCTGAGACGGGAGA A G HDAC1 Ensembl:ENSG00000116478 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1262188475 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_341211 30984 RMVar_ID_30984 Human_SNP_ID_8512034 A-to-I Human chr1 + 32318379 32318379 32318379 AGCCAGGAGTTTGAGACCAGCCTGGGCAACATAGTGAGACCCTCATCTCTACAAAAAAATAAAAA AGCCAGGAGTTTGAGACCAGCCTGGGCAACATGGTGAGACCCTCATCTCTACAAAAAAATAAAAA A G HDAC1 Ensembl:ENSG00000116478 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1241415268 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116794,RMVar_hsa_circ_131229 30985 RMVar_ID_30985 Human_SNP_ID_8512171 A-to-I Human chr1 + 32318937 32318937 32318937 GGTCGGGAGTTTGAGACCAGCCTGGCCAACATAGTGAAACCCCATCTCTACTAAAAATACAAAAA GGTCGGGAGTTTGAGACCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAA A G HDAC1 Ensembl:ENSG00000116478 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs552686 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116794,RMVar_hsa_circ_131229 30986 RMVar_ID_30986 Human_SNP_ID_8525686 A-to-I Human chr1 - 32369426 32369426 32369426 TAGCTCACTGCAGCCTTGAACTCCTGGGCTCAAGTGATCACCACACCTCAGCCTCCTGAGTAGCT TAGCTCACTGCAGCCTTGAACTCCTGGGCTCAGGTGATCACCACACCTCAGCCTCCTGAGTAGCT T C BSDC1 Ensembl:ENSG00000160058 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1002232386 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55523,RMVar_hsa_circ_312651,RMVar_hsa_circ_22951,RMVar_hsa_circ_35783,RMVar_hsa_circ_131246 30987 RMVar_ID_30987 Human_SNP_ID_8526204 A-to-I Human chr1 - 32371407 32371407 32371407 ACTCAGGAGGCTGAGGCAGGAGAATGGTGTGAACCCAGGAGGCAGAGCTTGCAGTGAGCCGAGAT ACTCAGGAGGCTGAGGCAGGAGAATGGTGTGAGCCCAGGAGGCAGAGCTTGCAGTGAGCCGAGAT T C BSDC1 Ensembl:ENSG00000160058 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1228775158 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55523,RMVar_hsa_circ_312651,RMVar_hsa_circ_22951,RMVar_hsa_circ_35783,RMVar_hsa_circ_131246 30988 RMVar_ID_30988 Human_SNP_ID_8526210 A-to-I Human chr1 - 32371435 32371435 32371435 GTGGTGGCGGGCGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATGGTGTGAACCCA GTGGTGGCGGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGTGTGAACCCA T C BSDC1 Ensembl:ENSG00000160058 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs948616976 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55523,RMVar_hsa_circ_312651,RMVar_hsa_circ_22951,RMVar_hsa_circ_35783,RMVar_hsa_circ_131246 30989 RMVar_ID_30989 Human_SNP_ID_8526212 A-to-I Human chr1 - 32371439 32371439 32371439 GGGCGTGGTGGCGGGCGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATGGTGTGAA GGGCGTGGTGGCGGGCGCCTGTAGTCCCAGCTGCTCAGGAGGCTGAGGCAGGAGAATGGTGTGAA T C BSDC1 Ensembl:ENSG00000160058 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1055318504 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55523,RMVar_hsa_circ_312651,RMVar_hsa_circ_22951,RMVar_hsa_circ_35783,RMVar_hsa_circ_131246 30990 RMVar_ID_30990 Human_SNP_ID_8526228 A-to-I Human chr1 - 32371479 32371479 32371479 GGTGAAACCCCATCTCTACTAAAAATATAAAAAATTAGCCGGGCGTGGTGGCGGGCGCCTGTAGT GGTGAAACCCCATCTCTACTAAAAATATAAAAGATTAGCCGGGCGTGGTGGCGGGCGCCTGTAGT T C BSDC1 Ensembl:ENSG00000160058 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs577672104 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55523,RMVar_hsa_circ_312651,RMVar_hsa_circ_22951,RMVar_hsa_circ_35783,RMVar_hsa_circ_131246 30991 RMVar_ID_30991 Human_SNP_ID_8526230 A-to-I Human chr1 - 32371488 32371488 32371488 GGCTAACACGGTGAAACCCCATCTCTACTAAAAATATAAAAAATTAGCCGGGCGTGGTGGCGGGC GGCTAACACGGTGAAACCCCATCTCTACTAAACATATAAAAAATTAGCCGGGCGTGGTGGCGGGC T G BSDC1 Ensembl:ENSG00000160058 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1019730775 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55523,RMVar_hsa_circ_312651,RMVar_hsa_circ_22951,RMVar_hsa_circ_35783,RMVar_hsa_circ_131246 30992 RMVar_ID_30992 Human_SNP_ID_8526233 A-to-I Human chr1 - 32371500 32371500 32371500 CGAGACCATCCTGGCTAACACGGTGAAACCCCATCTCTACTAAAAATATAAAAAATTAGCCGGGC CGAGACCATCCTGGCTAACACGGTGAAACCCCGTCTCTACTAAAAATATAAAAAATTAGCCGGGC T C BSDC1 Ensembl:ENSG00000160058 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1475632188 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55523,RMVar_hsa_circ_312651,RMVar_hsa_circ_22951,RMVar_hsa_circ_35783,RMVar_hsa_circ_131246 30993 RMVar_ID_30993 Human_SNP_ID_8570223 A-to-I Human chr1 + 32553629 32553629 32553629 AATTCTGGGGCCGGGCGCGGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGTCAAGGCAGAC AATTCTGGGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGTCAAGGCAGAC A G ZBTB8A,AL033529.1 Ensembl:ENSG00000160062,Ensembl:ENSG00000254553 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1001506869 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103986,RMVar_hsa_circ_114995,RMVar_hsa_circ_131250,RMVar_hsa_circ_131251,RMVar_hsa_circ_116159,RMVar_hsa_circ_118785,RMVar_hsa_circ_131253,RMVar_hsa_circ_131256,RMVar_hsa_circ_131258,RMVar_hsa_circ_332692,RMVar_hsa_circ_131255,RMVar_hsa_circ_309677,RMVar_hsa_circ_131257 30994 RMVar_ID_30994 Human_SNP_ID_8570366 A-to-I Human chr1 + 32554077 32554077 32554077 CAAAAATTAGCCGGGCGTGGTGCTGGGCGCCTATAATCCCAGGTGCTTGTGAGGCTGAGACAGGA CAAAAATTAGCCGGGCGTGGTGCTGGGCGCCTCTAATCCCAGGTGCTTGTGAGGCTGAGACAGGA A C ZBTB8A,AL033529.1 Ensembl:ENSG00000160062,Ensembl:ENSG00000254553 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1040727404 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103986,RMVar_hsa_circ_114995,RMVar_hsa_circ_131250,RMVar_hsa_circ_131251,RMVar_hsa_circ_116159,RMVar_hsa_circ_118785,RMVar_hsa_circ_131253,RMVar_hsa_circ_131256,RMVar_hsa_circ_131258,RMVar_hsa_circ_332692,RMVar_hsa_circ_131255,RMVar_hsa_circ_309677,RMVar_hsa_circ_131257 30995 RMVar_ID_30995 Human_SNP_ID_8570367 A-to-I Human chr1 + 32554077 32554077 32554077 CAAAAATTAGCCGGGCGTGGTGCTGGGCGCCTATAATCCCAGGTGCTTGTGAGGCTGAGACAGGA CAAAAATTAGCCGGGCGTGGTGCTGGGCGCCTGTAATCCCAGGTGCTTGTGAGGCTGAGACAGGA A G ZBTB8A,AL033529.1 Ensembl:ENSG00000160062,Ensembl:ENSG00000254553 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1040727404 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103986,RMVar_hsa_circ_114995,RMVar_hsa_circ_131250,RMVar_hsa_circ_131251,RMVar_hsa_circ_116159,RMVar_hsa_circ_118785,RMVar_hsa_circ_131253,RMVar_hsa_circ_131256,RMVar_hsa_circ_131258,RMVar_hsa_circ_332692,RMVar_hsa_circ_131255,RMVar_hsa_circ_309677,RMVar_hsa_circ_131257 30996 RMVar_ID_30996 Human_SNP_ID_8570536 A-to-I Human chr1 + 32554519 32554519 32554519 TATTTATTTATTTATTTATTTATTTATTTTTGAGATGTAGTCTGGCTCTGTCGGCCAGACTGGAG TATTTATTTATTTATTTATTTATTTATTTTTGTGATGTAGTCTGGCTCTGTCGGCCAGACTGGAG A T ZBTB8A,AL033529.1 Ensembl:ENSG00000160062,Ensembl:ENSG00000254553 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1158240655 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103986,RMVar_hsa_circ_114995,RMVar_hsa_circ_131250,RMVar_hsa_circ_131251,RMVar_hsa_circ_116159,RMVar_hsa_circ_118785,RMVar_hsa_circ_131253,RMVar_hsa_circ_131256,RMVar_hsa_circ_131258,RMVar_hsa_circ_332692,RMVar_hsa_circ_131255,RMVar_hsa_circ_309677,RMVar_hsa_circ_131257 30997 RMVar_ID_30997 Human_SNP_ID_8576458 A-to-I Human chr1 + 32578791 32578791 32578791 GTGGCTATTTACAGGTGTGATCATAGCGCGCTACAGCCTCTAACTCCTGGACTCAAGCGATCCTG GTGGCTATTTACAGGTGTGATCATAGCGCGCTCCAGCCTCTAACTCCTGGACTCAAGCGATCCTG A C ZBTB8A,AL033529.1 Ensembl:ENSG00000160062,Ensembl:ENSG00000254553 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1409429479 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103986,RMVar_hsa_circ_114995,RMVar_hsa_circ_131250,RMVar_hsa_circ_131251,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 30998 RMVar_ID_30998 Human_SNP_ID_8582110 A-to-I Human chr1 + 32601247 32601247 32601247 CCTATAATCCCAATACTTTGGGAGGCCGAGGCAGGCGGATCACAAGGTCAGGAGTTTGAAACCAG CCTATAATCCCAATACTTTGGGAGGCCGAGGCGGGCGGATCACAAGGTCAGGAGTTTGAAACCAG A G ZBTB8A Ensembl:ENSG00000160062 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1447609437 Functional Loss SNV dbSNP153 33..33 33 - - - 30999 RMVar_ID_30999 Human_SNP_ID_8582113 A-to-I Human chr1 + 32601258 32601258 32601258 AATACTTTGGGAGGCCGAGGCAGGCGGATCACAAGGTCAGGAGTTTGAAACCAGCCTGGCCAACA AATACTTTGGGAGGCCGAGGCAGGCGGATCACGAGGTCAGGAGTTTGAAACCAGCCTGGCCAACA A G ZBTB8A Ensembl:ENSG00000160062 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1397699380 Functional Loss SNV dbSNP153 33..33 33 - - - 31000 RMVar_ID_31000 Human_SNP_ID_8582360 A-to-I Human chr1 + 32602213 32602213 32602213 AGCCGGGCGTGGTGGTGCATGCCTGTAATCCCAGCTACTCAGAAGGCTGAGGCAGGAGGATAGCT AGCCGGGCGTGGTGGTGCATGCCTGTAATCCCGGCTACTCAGAAGGCTGAGGCAGGAGGATAGCT A G ZBTB8A Ensembl:ENSG00000160062 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1483444276 Functional Loss SNV dbSNP153 33..33 33 - - - 31001 RMVar_ID_31001 Human_SNP_ID_8582365 A-to-I Human chr1 + 32602221 32602221 32602221 GTGGTGGTGCATGCCTGTAATCCCAGCTACTCAGAAGGCTGAGGCAGGAGGATAGCTTGAACCCA GTGGTGGTGCATGCCTGTAATCCCAGCTACTCGGAAGGCTGAGGCAGGAGGATAGCTTGAACCCA A G ZBTB8A Ensembl:ENSG00000160062 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432850499 Functional Loss SNV dbSNP153 33..33 33 - - - 31002 RMVar_ID_31002 Human_SNP_ID_8582371 A-to-I Human chr1 + 32602242 32602242 32602242 CCCAGCTACTCAGAAGGCTGAGGCAGGAGGATAGCTTGAACCCAGGAGGCAGAGGCTGCGGTGGG CCCAGCTACTCAGAAGGCTGAGGCAGGAGGATGGCTTGAACCCAGGAGGCAGAGGCTGCGGTGGG A G ZBTB8A Ensembl:ENSG00000160062 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1442366620 Functional Loss SNV dbSNP153 33..33 33 - - - 31003 RMVar_ID_31003 Human_SNP_ID_8582372 A-to-I Human chr1 + 32602253 32602253 32602253 AGAAGGCTGAGGCAGGAGGATAGCTTGAACCCAGGAGGCAGAGGCTGCGGTGGGCTGAGGTTGCG AGAAGGCTGAGGCAGGAGGATAGCTTGAACCCGGGAGGCAGAGGCTGCGGTGGGCTGAGGTTGCG A G ZBTB8A Ensembl:ENSG00000160062 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1400587503 Functional Loss SNV dbSNP153 33..33 33 - - - 31004 RMVar_ID_31004 Human_SNP_ID_8582576 A-to-I Human chr1 + 32602812 32602812 32602812 TGATCTCGTGATCCGCCCCCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCGC TGATCTCGTGATCCGCCCCCCTCGGCCTCCCAGAGTGCTGGGATTACAGGCGTGAGCCACTGCGC A G ZBTB8A Ensembl:ENSG00000160062 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1258275063 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_101979 31005 RMVar_ID_31005 Human_SNP_ID_8583179 A-to-I Human chr1 + 32605426 32605426 32605426 GAGGCACAGAACAGTAAAAAAACCTCAGGGTCAGGCGTGGTGGCTCACACCTGTAATCCCAGCAC GAGGCACAGAACAGTAAAAAAACCTCAGGGTCGGGCGTGGTGGCTCACACCTGTAATCCCAGCAC A G ZBTB8A Ensembl:ENSG00000160062 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1353867854 Functional Loss SNV dbSNP153 33..33 33 - - - 31006 RMVar_ID_31006 Human_SNP_ID_8583186 A-to-I Human chr1 + 32605442 32605442 32605442 AAAAAACCTCAGGGTCAGGCGTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGC AAAAAACCTCAGGGTCAGGCGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGC A G ZBTB8A Ensembl:ENSG00000160062 Protein coding 3'UTR GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs1211237706 Functional Loss SNV dbSNP153 33..33 33 - - - 31007 RMVar_ID_31007 Human_SNP_ID_8585989 A-to-I Human chr1 - 32616549 32616549 32616549 CTCCTGCCTCAGCCTCCCGAGTAGCTTGGACTACAGGCGCCTGCCACCACGCCCAGCTAATTTTG CTCCTGCCTCAGCCTCCCGAGTAGCTTGGACTGCAGGCGCCTGCCACCACGCCCAGCTAATTTTG T C ZBTB8OS Ensembl:ENSG00000176261 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1029927794 Functional Loss SNV dbSNP153 33..33 33 - - - 31008 RMVar_ID_31008 Human_SNP_ID_8586997 A-to-I Human chr1 - 32620601 32620601 32620601 ACCATACCTGGCTAATTTTTAAATTTTTTTGTAGAGACAGGGTCTCACTATGTTGTCTTGAACTG ACCATACCTGGCTAATTTTTAAATTTTTTTGTGGAGACAGGGTCTCACTATGTTGTCTTGAACTG T C ZBTB8OS Ensembl:ENSG00000176261 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs779103605 Functional Loss SNV dbSNP153 33..33 33 - - - 31009 RMVar_ID_31009 Human_SNP_ID_8587048 A-to-I Human chr1 - 32620766 32620758 32620767 TTAACTACTTAAGCTATTCGTCCTTTTTTTTGAGACAGGGTCTTGCTCTGTCCCCCAGGCTGGAA TTAACTACTTAAGCTATTCGTCCTTTTTTTT_________TCTTGCTCTGTCCCCCAGGCTGGAA ACCCTGTCTC A ZBTB8OS Ensembl:ENSG00000176261 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1325764604 Functional Loss DEL dbSNP153 32..40 33 - - - Human_RBP_ID_10944241 31010 RMVar_ID_31010 Human_SNP_ID_8587176 A-to-I Human chr1 - 32621211 32621211 32621211 TATCTTTAGTAGAGACGGGGTTTCACTGTGTTAGCTAGGATGGTCTTGATCTCCTGACCTTGTGA TATCTTTAGTAGAGACGGGGTTTCACTGTGTTGGCTAGGATGGTCTTGATCTCCTGACCTTGTGA T C ZBTB8OS Ensembl:ENSG00000176261 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1132212 Functional Loss SNV dbSNP153 33..33 33 - - - 31011 RMVar_ID_31011 Human_SNP_ID_8587205 A-to-I Human chr1 - 32621275 32621274 32621275 CCTACCTCAGCCTCCCGAGTAGCTGGGACTATAGGCACCCGCCACCATGCCCGGCTAATTTTTGT CCTACCTCAGCCTCCCGAGTAGCTGGGACTAT_GGCACCCGCCACCATGCCCGGCTAATTTTTGT CT C ZBTB8OS Ensembl:ENSG00000176261 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1257003340 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_352705 31012 RMVar_ID_31012 Human_SNP_ID_8587206 A-to-I Human chr1 - 32621275 32621275 32621275 CCTACCTCAGCCTCCCGAGTAGCTGGGACTATAGGCACCCGCCACCATGCCCGGCTAATTTTTGT CCTACCTCAGCCTCCCGAGTAGCTGGGACTATGGGCACCCGCCACCATGCCCGGCTAATTTTTGT T C ZBTB8OS Ensembl:ENSG00000176261 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1132213 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_352705 31013 RMVar_ID_31013 Human_SNP_ID_8587227 A-to-I Human chr1 - 32621336 32621336 32621336 GAAGCGCAGTGGTGTGAGCTCGGCTTACTGCAAGCTCCACCTCCCGGGTTCACGCCATTCTCCTA GAAGCGCAGTGGTGTGAGCTCGGCTTACTGCAGGCTCCACCTCCCGGGTTCACGCCATTCTCCTA T C ZBTB8OS Ensembl:ENSG00000176261 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1192378629 Functional Loss SNV dbSNP153 33..33 33 - - - 31014 RMVar_ID_31014 Human_SNP_ID_8587240 A-to-I Human chr1 - 32621367 32621367 32621367 TGAGACGGAGTCTCGCTCTGTAGCCCAGGCTGAAGCGCAGTGGTGTGAGCTCGGCTTACTGCAAG TGAGACGGAGTCTCGCTCTGTAGCCCAGGCTGGAGCGCAGTGGTGTGAGCTCGGCTTACTGCAAG T C ZBTB8OS Ensembl:ENSG00000176261 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1450501224 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_352706,Human_RBP_ID_10944248 31015 RMVar_ID_31015 Human_SNP_ID_8588144 A-to-I Human chr1 - 32625123 32625123 32625123 CCCCTCCCAGGTTCAAGCGATTCTCGTGTCTCAGCCTCCCGAGTAGCTGGGATTACAGGCCCATG CCCCTCCCAGGTTCAAGCGATTCTCGTGTCTCTGCCTCCCGAGTAGCTGGGATTACAGGCCCATG T A ZBTB8OS Ensembl:ENSG00000176261 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1238569492 Functional Loss SNV dbSNP153 33..33 33 - - - 31016 RMVar_ID_31016 Human_SNP_ID_8588145 A-to-I Human chr1 - 32625123 32625123 32625123 CCCCTCCCAGGTTCAAGCGATTCTCGTGTCTCAGCCTCCCGAGTAGCTGGGATTACAGGCCCATG CCCCTCCCAGGTTCAAGCGATTCTCGTGTCTCCGCCTCCCGAGTAGCTGGGATTACAGGCCCATG T G ZBTB8OS Ensembl:ENSG00000176261 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1238569492 Functional Loss SNV dbSNP153 33..33 33 - - - 31017 RMVar_ID_31017 Human_SNP_ID_8589112 A-to-I Human chr1 - 32628860 32628860 32628860 GTGATCTTGGTTCACTGCAATGTCCGCCTCCCAGATTCAAACCATTCTTGTGCCTCAGCCTCCCG GTGATCTTGGTTCACTGCAATGTCCGCCTCCCGGATTCAAACCATTCTTGTGCCTCAGCCTCCCG T C ZBTB8OS Ensembl:ENSG00000176261 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1247520624 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10944454,Human_RBP_ID_17749009 RMVar_hsa_circ_99545,RMVar_hsa_circ_323226,RMVar_hsa_circ_377889,RMVar_hsa_circ_377826,RMVar_hsa_circ_289733,RMVar_hsa_circ_131265,RMVar_hsa_circ_131266 31018 RMVar_ID_31018 Human_SNP_ID_8589614 A-to-I Human chr1 - 32631003 32631003 32631003 TTTCATTTATTATTTATTTATTTATTTTTGAGACAGAGTCTCGCTCTGTTGCTCAGGCTGGAGTG TTTCATTTATTATTTATTTATTTATTTTTGAGGCAGAGTCTCGCTCTGTTGCTCAGGCTGGAGTG T C ZBTB8OS Ensembl:ENSG00000176261 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs915632505 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99545,RMVar_hsa_circ_323226,RMVar_hsa_circ_377889,RMVar_hsa_circ_377826,RMVar_hsa_circ_289733,RMVar_hsa_circ_131265,RMVar_hsa_circ_131266 31019 RMVar_ID_31019 Human_SNP_ID_8590199 A-to-I Human chr1 - 32633311 32633311 32633311 TGCTATGTTGTCGAGGCTAGTCTTGAACTCCTAGCTTCCGGCAATCCTCCTGCCTCAATTTTGCA TGCTATGTTGTCGAGGCTAGTCTTGAACTCCTGGCTTCCGGCAATCCTCCTGCCTCAATTTTGCA T C ZBTB8OS Ensembl:ENSG00000176261 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1165702567 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10944601 Human_Splice_Rec_43712,Human_Splice_Rec_43713 RMVar_hsa_circ_4558,RMVar_hsa_circ_99545,RMVar_hsa_circ_323226,RMVar_hsa_circ_377889,RMVar_hsa_circ_377826,RMVar_hsa_circ_289733,RMVar_hsa_circ_131265,RMVar_hsa_circ_131266,RMVar_hsa_circ_131268,RMVar_hsa_circ_279314,RMVar_hsa_circ_288096,RMVar_hsa_circ_274094,RMVar_hsa_circ_131267 31020 RMVar_ID_31020 Human_SNP_ID_8591388 A-to-I Human chr1 - 32637919 32637919 32637919 TGAGGTGGGAGAATCACTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCCAAGATCACTCCACTGC TGAGGTGGGAGAATCACTTGAACCTGGGAGGCTGAGGTTGCAGTGAGCCAAGATCACTCCACTGC T A ZBTB8OS Ensembl:ENSG00000176261 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6698213 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99545,RMVar_hsa_circ_131266 31021 RMVar_ID_31021 Human_SNP_ID_8591389 A-to-I Human chr1 - 32637919 32637919 32637919 TGAGGTGGGAGAATCACTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCCAAGATCACTCCACTGC TGAGGTGGGAGAATCACTTGAACCTGGGAGGCGGAGGTTGCAGTGAGCCAAGATCACTCCACTGC T C ZBTB8OS Ensembl:ENSG00000176261 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6698213 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99545,RMVar_hsa_circ_131266 31022 RMVar_ID_31022 Human_SNP_ID_8591393 A-to-I Human chr1 - 32637958 32637958 32637958 ATGGTGGTGGACTCCTGTGATCCCAGGTACTCAGGAGGTTGAGGTGGGAGAATCACTTGAACCTG ATGGTGGTGGACTCCTGTGATCCCAGGTACTCCGGAGGTTGAGGTGGGAGAATCACTTGAACCTG T G ZBTB8OS Ensembl:ENSG00000176261 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs12146017 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99545,RMVar_hsa_circ_131266 31023 RMVar_ID_31023 Human_SNP_ID_8591434 A-to-I Human chr1 - 32638083 32638083 32638083 CCTGTAATCCCAGCACTTTGGGAAGCCAGTGTAGGTGGTTCACCTGAGATTAGACGTTTGAGACC CCTGTAATCCCAGCACTTTGGGAAGCCAGTGTGGGTGGTTCACCTGAGATTAGACGTTTGAGACC T C ZBTB8OS Ensembl:ENSG00000176261 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs186806135 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10944716 RMVar_hsa_circ_99545,RMVar_hsa_circ_131266 31024 RMVar_ID_31024 Human_SNP_ID_8591435 A-to-I Human chr1 - 32638083 32638083 32638083 CCTGTAATCCCAGCACTTTGGGAAGCCAGTGTAGGTGGTTCACCTGAGATTAGACGTTTGAGACC CCTGTAATCCCAGCACTTTGGGAAGCCAGTGTCGGTGGTTCACCTGAGATTAGACGTTTGAGACC T G ZBTB8OS Ensembl:ENSG00000176261 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs186806135 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10944716 RMVar_hsa_circ_99545,RMVar_hsa_circ_131266 31025 RMVar_ID_31025 Human_SNP_ID_8591604 A-to-I Human chr1 - 32638741 32638741 32638741 CCCAGCTAATTTTTTCTATTTTCAGTAGAGACAGCGTTTCACCATGTTGGCCAGGCTGTTCTCGA CCCAGCTAATTTTTTCTATTTTCAGTAGAGACGGCGTTTCACCATGTTGGCCAGGCTGTTCTCGA T C ZBTB8OS Ensembl:ENSG00000176261 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1399444464 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99545,RMVar_hsa_circ_131266 31026 RMVar_ID_31026 Human_SNP_ID_8591606 A-to-I Human chr1 - 32638747 32638747 32638747 ACTATCCCCAGCTAATTTTTTCTATTTTCAGTAGAGACAGCGTTTCACCATGTTGGCCAGGCTGT ACTATCCCCAGCTAATTTTTTCTATTTTCAGTGGAGACAGCGTTTCACCATGTTGGCCAGGCTGT T C ZBTB8OS Ensembl:ENSG00000176261 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1337438672 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99545,RMVar_hsa_circ_131266 31027 RMVar_ID_31027 Human_SNP_ID_8591617 A-to-I Human chr1 - 32638792 32638792 32638792 TTCATGCTTCAGCCTCCCAAGTAGCTGGGATTACAGGGTTGTGCCACTATCCCCAGCTAATTTTT TTCATGCTTCAGCCTCCCAAGTAGCTGGGATTCCAGGGTTGTGCCACTATCCCCAGCTAATTTTT T G ZBTB8OS Ensembl:ENSG00000176261 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1557793132 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99545,RMVar_hsa_circ_131266 31028 RMVar_ID_31028 Human_SNP_ID_8591629 A-to-I Human chr1 - 32638851 32638851 32638851 GGAGTGCAGTAGTGCGATCTCAACTCATTGCAACCTTTGCCACCTGGGTTCAAGCGATTTTCATG GGAGTGCAGTAGTGCGATCTCAACTCATTGCAGCCTTTGCCACCTGGGTTCAAGCGATTTTCATG T C ZBTB8OS Ensembl:ENSG00000176261 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1208916828 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99545,RMVar_hsa_circ_131266 31029 RMVar_ID_31029 Human_SNP_ID_8591806 A-to-I Human chr1 - 32639650 32639650 32639650 GGGTCAGGCAGTCCTCCCCATCTCAGCCTCCCAAGTAGCTGGGACTACAGGCATGCACTACCACG GGGTCAGGCAGTCCTCCCCATCTCAGCCTCCCGAGTAGCTGGGACTACAGGCATGCACTACCACG T C ZBTB8OS Ensembl:ENSG00000176261 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1255504123 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99545,RMVar_hsa_circ_131266 31030 RMVar_ID_31030 Human_SNP_ID_8591812 A-to-I Human chr1 - 32639683 32639683 32639683 TGCACTCTTAGCTCACTGCAGCCCAAGCTCCTAGGGTCAGGCAGTCCTCCCCATCTCAGCCTCCC TGCACTCTTAGCTCACTGCAGCCCAAGCTCCTGGGGTCAGGCAGTCCTCCCCATCTCAGCCTCCC T C ZBTB8OS Ensembl:ENSG00000176261 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs750262995 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99545,RMVar_hsa_circ_131266 31031 RMVar_ID_31031 Human_SNP_ID_8591819 A-to-I Human chr1 - 32639726 32639726 32639726 AGTTGGGACCTTACTCTGTTGCCCACACTGGAATGCAGCTCACTGCACTCTTAGCTCACTGCAGC AGTTGGGACCTTACTCTGTTGCCCACACTGGAGTGCAGCTCACTGCACTCTTAGCTCACTGCAGC T C ZBTB8OS Ensembl:ENSG00000176261 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1396682213 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10944743 RMVar_hsa_circ_99545,RMVar_hsa_circ_131266 31032 RMVar_ID_31032 Human_SNP_ID_8591959 A-to-I Human chr1 - 32640303 32640303 32640303 GAGGTCAGGAGTTCGAGACCAGTCTGACTAACATGGTGAAACCCCGTCTCTACTAAAAATACAAA GAGGTCAGGAGTTCGAGACCAGTCTGACTAACGTGGTGAAACCCCGTCTCTACTAAAAATACAAA T C ZBTB8OS Ensembl:ENSG00000176261 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs760077407 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99545,RMVar_hsa_circ_131266 31033 RMVar_ID_31033 Human_SNP_ID_8592025 A-to-I Human chr1 - 32640597 32640597 32640597 GGCAGAAGTATCACTTGGACCTTGGAGGTCTAAGCTGTAGTGAGCTGTGATTGTGCCACTGCACT GGCAGAAGTATCACTTGGACCTTGGAGGTCTAGGCTGTAGTGAGCTGTGATTGTGCCACTGCACT T C ZBTB8OS Ensembl:ENSG00000176261 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs76448536 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99545,RMVar_hsa_circ_131266 31034 RMVar_ID_31034 Human_SNP_ID_8592041 A-to-I Human chr1 - 32640676 32640676 32640676 GGCAAAACCCTGTCTCTTACAAAACATTAACTAGGTGTGGTGGTGCGTGTCTGTAGTCCTTACCA GGCAAAACCCTGTCTCTTACAAAACATTAACTGGGTGTGGTGGTGCGTGTCTGTAGTCCTTACCA T C ZBTB8OS Ensembl:ENSG00000176261 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1033458935 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10944760 RMVar_hsa_circ_99545,RMVar_hsa_circ_131266 31035 RMVar_ID_31035 Human_SNP_ID_8592512 A-to-I Human chr1 - 32642247 32642247 32642247 TGCCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGTATGAACCACCGCGCCCGGCCCTGGCCA TGCCTGCCTTGGCCTCCCAAAGTGCTGGGATTGCAGGTATGAACCACCGCGCCCGGCCCTGGCCA T C ZBTB8OS Ensembl:ENSG00000176261 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1017668261 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10944772 RMVar_hsa_circ_99545,RMVar_hsa_circ_131266 31036 RMVar_ID_31036 Human_SNP_ID_8592543 A-to-I Human chr1 - 32642338 32642338 32642338 CACTACGCCCAGCTAATTTTTGCATTTTTAGTAGATACGGGGTTTCACCACGTTGGCCAGGCTGG CACTACGCCCAGCTAATTTTTGCATTTTTAGTGGATACGGGGTTTCACCACGTTGGCCAGGCTGG T C ZBTB8OS Ensembl:ENSG00000176261 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs868044670 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99545,RMVar_hsa_circ_131266 31037 RMVar_ID_31037 Human_SNP_ID_8592737 A-to-I Human chr1 - 32642950 32642950 32642950 CCTGGCCAACATGGTGAAACTCTGTCTCTACTAAAAATACAAAAATTAGCCGTGCGTGGTGGCGC CCTGGCCAACATGGTGAAACTCTGTCTCTACTTAAAATACAAAAATTAGCCGTGCGTGGTGGCGC T A ZBTB8OS Ensembl:ENSG00000176261 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2934768 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10944785 RMVar_hsa_circ_99545,RMVar_hsa_circ_131266 31038 RMVar_ID_31038 Human_SNP_ID_8592738 A-to-I Human chr1 - 32642950 32642950 32642950 CCTGGCCAACATGGTGAAACTCTGTCTCTACTAAAAATACAAAAATTAGCCGTGCGTGGTGGCGC CCTGGCCAACATGGTGAAACTCTGTCTCTACTGAAAATACAAAAATTAGCCGTGCGTGGTGGCGC T C ZBTB8OS Ensembl:ENSG00000176261 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2934768 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10944785 RMVar_hsa_circ_99545,RMVar_hsa_circ_131266 31039 RMVar_ID_31039 Human_SNP_ID_8592739 A-to-I Human chr1 - 32642950 32642950 32642950 CCTGGCCAACATGGTGAAACTCTGTCTCTACTAAAAATACAAAAATTAGCCGTGCGTGGTGGCGC CCTGGCCAACATGGTGAAACTCTGTCTCTACTCAAAATACAAAAATTAGCCGTGCGTGGTGGCGC T G ZBTB8OS Ensembl:ENSG00000176261 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2934768 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10944785 RMVar_hsa_circ_99545,RMVar_hsa_circ_131266 31040 RMVar_ID_31040 Human_SNP_ID_8593279 A-to-I Human chr1 - 32644653 32644652 32644653 GTGTGTAGTCCTGTAGTCGCACCTACTGGGGAAGCTGAGCCAGAAGGATTGTTTGAGCTCAGGCG GTGTGTAGTCCTGTAGTCGCACCTACTGGGGA_GCTGAGCCAGAAGGATTGTTTGAGCTCAGGCG CT C ZBTB8OS Ensembl:ENSG00000176261 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1269814158 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_10944811 RMVar_hsa_circ_99545,RMVar_hsa_circ_131266 31041 RMVar_ID_31041 Human_SNP_ID_8593332 A-to-I Human chr1 - 32644772 32644772 32644772 GGGAGGCCTAAGCCGGAGGATTTCTTGAACCCAGGATTTCCAGATTAGTCTGGGCAACACAGTGA GGGAGGCCTAAGCCGGAGGATTTCTTGAACCCGGGATTTCCAGATTAGTCTGGGCAACACAGTGA T C ZBTB8OS Ensembl:ENSG00000176261 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1323368942 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10944814,Human_RBP_ID_17557106 RMVar_hsa_circ_99545,RMVar_hsa_circ_131266 31042 RMVar_ID_31042 Human_SNP_ID_8593487 A-to-I Human chr1 - 32645426 32645426 32645426 GCTGTCATGGCTCACTGCAAGCTTGAGCTCCTAGGCTCAAGCTGTTCTCCCACCTCAGCCTCCTG GCTGTCATGGCTCACTGCAAGCTTGAGCTCCTGGGCTCAAGCTGTTCTCCCACCTCAGCCTCCTG T C ZBTB8OS Ensembl:ENSG00000176261 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1436962286 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99545,RMVar_hsa_circ_131266 31043 RMVar_ID_31043 Human_SNP_ID_8593678 A-to-I Human chr1 - 32646259 32646259 32646259 GGAGTAGTGCAGTGGTGCGACTTTGACTCACTACAACCTCTGCCTCCTGGACTCAAGTGATCCTC GGAGTAGTGCAGTGGTGCGACTTTGACTCACTGCAACCTCTGCCTCCTGGACTCAAGTGATCCTC T C ZBTB8OS Ensembl:ENSG00000176261 Protein coding intron GSE38233;GSE100210;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 24183664,29129909,30559470 RNA-Seq:(High) rs1016217251 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10944847 RMVar_hsa_circ_99545,RMVar_hsa_circ_131266 31044 RMVar_ID_31044 Human_SNP_ID_8593694 A-to-I Human chr1 - 32646308 32646308 32646308 AAAATCTTTTTTTTTTTCCCTGAGACAGTCTCATTCTGTCACCCAAGCTGGAGTAGTGCAGTGGT AAAATCTTTTTTTTTTTCCCTGAGACAGTCTCTTTCTGTCACCCAAGCTGGAGTAGTGCAGTGGT T A ZBTB8OS Ensembl:ENSG00000176261 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs786294 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99545,RMVar_hsa_circ_131266 31045 RMVar_ID_31045 Human_SNP_ID_8593695 A-to-I Human chr1 - 32646308 32646308 32646308 AAAATCTTTTTTTTTTTCCCTGAGACAGTCTCATTCTGTCACCCAAGCTGGAGTAGTGCAGTGGT AAAATCTTTTTTTTTTTCCCTGAGACAGTCTCGTTCTGTCACCCAAGCTGGAGTAGTGCAGTGGT T C ZBTB8OS Ensembl:ENSG00000176261 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs786294 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99545,RMVar_hsa_circ_131266 31046 RMVar_ID_31046 Human_SNP_ID_8593696 A-to-I Human chr1 - 32646308 32646308 32646308 AAAATCTTTTTTTTTTTCCCTGAGACAGTCTCATTCTGTCACCCAAGCTGGAGTAGTGCAGTGGT AAAATCTTTTTTTTTTTCCCTGAGACAGTCTCCTTCTGTCACCCAAGCTGGAGTAGTGCAGTGGT T G ZBTB8OS Ensembl:ENSG00000176261 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs786294 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99545,RMVar_hsa_circ_131266 31047 RMVar_ID_31047 Human_SNP_ID_8593874 A-to-I Human chr1 - 32646874 32646874 32646874 CCACACCCGGCTAATTTTTGTGTTTTTTTTTTAGTAGAGACAGGGTTTCACCATGCTGGCCAGGA CCACACCCGGCTAATTTTTGTGTTTTTTTTTTGGTAGAGACAGGGTTTCACCATGCTGGCCAGGA T C ZBTB8OS Ensembl:ENSG00000176261 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs533974311 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99545,RMVar_hsa_circ_131266 31048 RMVar_ID_31048 Human_SNP_ID_8595831 A-to-I Human chr1 + 32652667 32652667 32652667 GATTCGAGCGATTCTCCTGCCTAAGCCCTCCCAAGTAGCTGGGATTACAGGCACCTGCCACCACG GATTCGAGCGATTCTCCTGCCTAAGCCCTCCCCAGTAGCTGGGATTACAGGCACCTGCCACCACG A C RBBP4 Ensembl:ENSG00000162521 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1439179069 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_131272,RMVar_hsa_circ_309059,RMVar_hsa_circ_366909,RMVar_hsa_circ_370393,RMVar_hsa_circ_131273,RMVar_hsa_circ_378233 31049 RMVar_ID_31049 Human_SNP_ID_8596336 A-to-I Human chr1 + 32654088 32654088 32654088 TTTCAGTGGTAATTCAAACCATTTAGGAACTTATGGGCTGGTCATGGTGGCTCACACGTGTAATC TTTCAGTGGTAATTCAAACCATTTAGGAACTTGTGGGCTGGTCATGGTGGCTCACACGTGTAATC A G RBBP4 Ensembl:ENSG00000162521 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1748048 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_131272,RMVar_hsa_circ_309059,RMVar_hsa_circ_366909,RMVar_hsa_circ_370393,RMVar_hsa_circ_131273,RMVar_hsa_circ_378233 31050 RMVar_ID_31050 Human_SNP_ID_8596352 A-to-I Human chr1 + 32654163 32654163 32654163 GGGAGGCTGAGGCAGGCAGATTGCTTGAGGCCAGGAGTTCCAGACCAGCCTGGGCAACATGGTGA GGGAGGCTGAGGCAGGCAGATTGCTTGAGGCCGGGAGTTCCAGACCAGCCTGGGCAACATGGTGA A G RBBP4 Ensembl:ENSG00000162521 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs966213155 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_131272,RMVar_hsa_circ_309059,RMVar_hsa_circ_366909,RMVar_hsa_circ_370393,RMVar_hsa_circ_131273,RMVar_hsa_circ_378233 31051 RMVar_ID_31051 Human_SNP_ID_8596708 A-to-I Human chr1 + 32655440 32655440 32655440 GGTTGTAGTTCTGTAACACTGTCCTCTCCTTCATTCTTTTTCTGGTTCTTGTCTAACCTTCTACA GGTTGTAGTTCTGTAACACTGTCCTCTCCTTCGTTCTTTTTCTGGTTCTTGTCTAACCTTCTACA A G RBBP4 Ensembl:ENSG00000162521 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2786172 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19342745,Human_RBP_ID_24685678 RMVar_hsa_circ_131272,RMVar_hsa_circ_309059,RMVar_hsa_circ_366909,RMVar_hsa_circ_370393,RMVar_hsa_circ_131273,RMVar_hsa_circ_378233 31052 RMVar_ID_31052 Human_SNP_ID_8597016 A-to-I Human chr1 + 32656486 32656486 32656486 GCAGTTCTCCTGTCGCAGCCTCCTGAGTAGCTAGGACTACAGGCACCGCCACCACACCCGGCTAA GCAGTTCTCCTGTCGCAGCCTCCTGAGTAGCTGGGACTACAGGCACCGCCACCACACCCGGCTAA A G RBBP4 Ensembl:ENSG00000162521 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1403648849 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10945174 RMVar_hsa_circ_131272,RMVar_hsa_circ_309059,RMVar_hsa_circ_366909,RMVar_hsa_circ_370393,RMVar_hsa_circ_131273,RMVar_hsa_circ_378233 31053 RMVar_ID_31053 Human_SNP_ID_8597207 A-to-I Human chr1 + 32657133 32657133 32657133 TCCCGTCTCTACTAAAAATACGAAAATCAGCCAGGCATGGTGGCAGGTTCTTGTAGTCCCAGCTA TCCCGTCTCTACTAAAAATACGAAAATCAGCCGGGCATGGTGGCAGGTTCTTGTAGTCCCAGCTA A G RBBP4 Ensembl:ENSG00000162521 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1457457976 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_131272,RMVar_hsa_circ_309059,RMVar_hsa_circ_366909,RMVar_hsa_circ_370393,RMVar_hsa_circ_131273,RMVar_hsa_circ_378233 31054 RMVar_ID_31054 Human_SNP_ID_8597426 A-to-I Human chr1 + 32657889 32657889 32657889 TGATTTTTTATTTTTTTACTCAGTCTCGCTCTATTGCCTAGGTTGGAGTGTAGTGGCACGATCTT TGATTTTTTATTTTTTTACTCAGTCTCGCTCTGTTGCCTAGGTTGGAGTGTAGTGGCACGATCTT A G RBBP4 Ensembl:ENSG00000162521 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1021780661 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2143650,Human_RBP_ID_10945232,Human_RBP_ID_18572323 RMVar_hsa_circ_309059,RMVar_hsa_circ_370393,RMVar_hsa_circ_131273,RMVar_hsa_circ_131274,RMVar_hsa_circ_322338,RMVar_hsa_circ_367390,RMVar_hsa_circ_59103 31055 RMVar_ID_31055 Human_SNP_ID_8597691 A-to-I Human chr1 + 32658728 32658728 32658728 ACCACCACGCCTGGCTAATTTTTTGTATTTTTAGTAGAGACAGGGTTTCATCATGTTGGTCAGGC ACCACCACGCCTGGCTAATTTTTTGTATTTTTGGTAGAGACAGGGTTTCATCATGTTGGTCAGGC A G RBBP4 Ensembl:ENSG00000162521 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1222574897 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_309059,RMVar_hsa_circ_370393,RMVar_hsa_circ_131273,RMVar_hsa_circ_131274,RMVar_hsa_circ_322338,RMVar_hsa_circ_367390,RMVar_hsa_circ_59103 31056 RMVar_ID_31056 Human_SNP_ID_8598039 A-to-I Human chr1 + 32659453 32659453 32659453 GCAGTGGCACGCACCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAAGAGCATCACTTGAACCCG GCAGTGGCACGCACCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAAGAGCATCACTTGAACCCG A G RBBP4 Ensembl:ENSG00000162521 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs902037127 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_309059,RMVar_hsa_circ_370393,RMVar_hsa_circ_131273,RMVar_hsa_circ_131274,RMVar_hsa_circ_322338,RMVar_hsa_circ_367390,RMVar_hsa_circ_59103 31057 RMVar_ID_31057 Human_SNP_ID_8598833 A-to-I Human chr1 + 32662025 32662025 32662025 CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGTCTGTGCCACCACACCCAGCTAATTTTT CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTGCAGGTCTGTGCCACCACACCCAGCTAATTTTT A G RBBP4 Ensembl:ENSG00000162521 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1466316551 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_309059,RMVar_hsa_circ_370393,RMVar_hsa_circ_131273,RMVar_hsa_circ_131274,RMVar_hsa_circ_322338,RMVar_hsa_circ_367390,RMVar_hsa_circ_59103 31058 RMVar_ID_31058 Human_SNP_ID_8599282 A-to-I Human chr1 + 32663471 32663471 32663471 TACTATATATGTATTTTTTCAGACAGGGTCTTACTCTGTTGCCCAGGCTGGAGTGCAGTGGTGTG TACTATATATGTATTTTTTCAGACAGGGTCTTGCTCTGTTGCCCAGGCTGGAGTGCAGTGGTGTG A G RBBP4 Ensembl:ENSG00000162521 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4245755 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_309059,RMVar_hsa_circ_370393,RMVar_hsa_circ_131273,RMVar_hsa_circ_131274,RMVar_hsa_circ_322338,RMVar_hsa_circ_367390,RMVar_hsa_circ_59103 31059 RMVar_ID_31059 Human_SNP_ID_8599283 A-to-I Human chr1 + 32663471 32663471 32663471 TACTATATATGTATTTTTTCAGACAGGGTCTTACTCTGTTGCCCAGGCTGGAGTGCAGTGGTGTG TACTATATATGTATTTTTTCAGACAGGGTCTTTCTCTGTTGCCCAGGCTGGAGTGCAGTGGTGTG A T RBBP4 Ensembl:ENSG00000162521 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4245755 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_309059,RMVar_hsa_circ_370393,RMVar_hsa_circ_131273,RMVar_hsa_circ_131274,RMVar_hsa_circ_322338,RMVar_hsa_circ_367390,RMVar_hsa_circ_59103 31060 RMVar_ID_31060 Human_SNP_ID_8599655 A-to-I Human chr1 + 32664552 32664552 32664552 TTGGTTCAGTGCAACCTCTGCCTCCCGGGTTCAAGCAATTCTCTTGCCTCAGTCTCCTGAGCAGC TTGGTTCAGTGCAACCTCTGCCTCCCGGGTTCGAGCAATTCTCTTGCCTCAGTCTCCTGAGCAGC A G RBBP4 Ensembl:ENSG00000162521 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215906923 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10945506 RMVar_hsa_circ_309059,RMVar_hsa_circ_370393,RMVar_hsa_circ_131273,RMVar_hsa_circ_131274,RMVar_hsa_circ_322338,RMVar_hsa_circ_367390,RMVar_hsa_circ_59103 31061 RMVar_ID_31061 Human_SNP_ID_8599677 A-to-I Human chr1 + 32664636 32664636 32664636 CACCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGATGAGGTTTCACCATATTGGCCATGCTGA CACCATGCCCAGCTAATTTTTGTATTTTTAGTGGAGATGAGGTTTCACCATATTGGCCATGCTGA A G RBBP4 Ensembl:ENSG00000162521 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1420153939 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_309059,RMVar_hsa_circ_370393,RMVar_hsa_circ_131273,RMVar_hsa_circ_131274,RMVar_hsa_circ_322338,RMVar_hsa_circ_367390,RMVar_hsa_circ_59103 31062 RMVar_ID_31062 Human_SNP_ID_8599902 A-to-I Human chr1 + 32665513 32665500 32665514 CAGTCTGGCCAACATGATGAAACCCCGTCTCTACTAAAAATGCAAAAATTAGCTGGGCGTCATGG CAGTCTGGCCAACATGATGA______________TAAAAATGCAAAAATTAGCTGGGCGTCATGG AAACCCCGTCTCTAC A RBBP4 Ensembl:ENSG00000162521 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1383310035 Functional Loss DEL dbSNP153 21..34 33 - - - RMVar_hsa_circ_309059,RMVar_hsa_circ_370393,RMVar_hsa_circ_131273,RMVar_hsa_circ_131274,RMVar_hsa_circ_322338,RMVar_hsa_circ_367390,RMVar_hsa_circ_59103 31063 RMVar_ID_31063 Human_SNP_ID_8599909 A-to-I Human chr1 + 32665513 32665513 32665513 CAGTCTGGCCAACATGATGAAACCCCGTCTCTACTAAAAATGCAAAAATTAGCTGGGCGTCATGG CAGTCTGGCCAACATGATGAAACCCCGTCTCTGCTAAAAATGCAAAAATTAGCTGGGCGTCATGG A G RBBP4 Ensembl:ENSG00000162521 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs940271268 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_309059,RMVar_hsa_circ_370393,RMVar_hsa_circ_131273,RMVar_hsa_circ_131274,RMVar_hsa_circ_322338,RMVar_hsa_circ_367390,RMVar_hsa_circ_59103 31064 RMVar_ID_31064 Human_SNP_ID_8600059 A-to-I Human chr1 + 32665989 32665989 32665989 ACATAATCACACATTATATTGTTATATATACTATAATGGTACTTGAGAGAACTCTCTAAGTGCAC ACATAATCACACATTATATTGTTATATATACTCTAATGGTACTTGAGAGAACTCTCTAAGTGCAC A C RBBP4 Ensembl:ENSG00000162521 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs675690 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1429471,Human_RBP_ID_10945573 RMVar_hsa_circ_309059,RMVar_hsa_circ_370393,RMVar_hsa_circ_131273,RMVar_hsa_circ_131274,RMVar_hsa_circ_322338,RMVar_hsa_circ_367390,RMVar_hsa_circ_59103 31065 RMVar_ID_31065 Human_SNP_ID_8600060 A-to-I Human chr1 + 32665989 32665989 32665989 ACATAATCACACATTATATTGTTATATATACTATAATGGTACTTGAGAGAACTCTCTAAGTGCAC ACATAATCACACATTATATTGTTATATATACTGTAATGGTACTTGAGAGAACTCTCTAAGTGCAC A G RBBP4 Ensembl:ENSG00000162521 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs675690 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1429471,Human_RBP_ID_10945573 RMVar_hsa_circ_309059,RMVar_hsa_circ_370393,RMVar_hsa_circ_131273,RMVar_hsa_circ_131274,RMVar_hsa_circ_322338,RMVar_hsa_circ_367390,RMVar_hsa_circ_59103 31066 RMVar_ID_31066 Human_SNP_ID_8601171 A-to-I Human chr1 + 32669922 32669922 32669922 CAAAAAAAAAGAAAAAAGAAAAACCTGGATGTATGAGTGGGCACACATGTGCTTTATGCCGTTGC CAAAAAAAAAGAAAAAAGAAAAACCTGGATGTGTGAGTGGGCACACATGTGCTTTATGCCGTTGC A G RBBP4 Ensembl:ENSG00000162521 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs359957 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_3487,GWAS_ID_3488,GWAS_ID_3489 RMVar_hsa_circ_5036,RMVar_hsa_circ_309059,RMVar_hsa_circ_322338,RMVar_hsa_circ_59103,RMVar_hsa_circ_131276,RMVar_hsa_circ_279080,RMVar_hsa_circ_10286,RMVar_hsa_circ_27413,RMVar_hsa_circ_128206,RMVar_hsa_circ_323087,RMVar_hsa_circ_131280 31067 RMVar_ID_31067 Human_SNP_ID_8601426 A-to-I Human chr1 + 32670712 32670712 32670712 CTCCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTAAGCCACCACGCCCAGCCGAGCCCA CTCCTGCCTCAGCCTCCCAAAGTGCTGGGATTGCAGGCGTAAGCCACCACGCCCAGCCGAGCCCA A G RBBP4 Ensembl:ENSG00000162521 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1417345511 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5036,RMVar_hsa_circ_309059,RMVar_hsa_circ_322338,RMVar_hsa_circ_59103,RMVar_hsa_circ_131276,RMVar_hsa_circ_279080,RMVar_hsa_circ_10286,RMVar_hsa_circ_27413,RMVar_hsa_circ_128206,RMVar_hsa_circ_323087,RMVar_hsa_circ_131280 31068 RMVar_ID_31068 Human_SNP_ID_8601612 A-to-I Human chr1 + 32671472 32671472 32671472 AGGCATGGTGGTGCACGCCTGTAATCCCAGCTACTTAAGAGGCTGAGGCAGGAGAATCGCTTGAA AGGCATGGTGGTGCACGCCTGTAATCCCAGCTTCTTAAGAGGCTGAGGCAGGAGAATCGCTTGAA A T RBBP4 Ensembl:ENSG00000162521 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1156250695 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5036,RMVar_hsa_circ_309059,RMVar_hsa_circ_322338,RMVar_hsa_circ_59103,RMVar_hsa_circ_131276,RMVar_hsa_circ_279080,RMVar_hsa_circ_10286,RMVar_hsa_circ_27413,RMVar_hsa_circ_128206,RMVar_hsa_circ_323087,RMVar_hsa_circ_131280 31069 RMVar_ID_31069 Human_SNP_ID_8602272 A-to-I Human chr1 + 32673567 32673567 32673567 TCGATCGATTCTCCTGCCTCAGCCTTCTGAGTAGCTGGGACTATAGGTGCGTACCACCATGCCTG TCGATCGATTCTCCTGCCTCAGCCTTCTGAGTTGCTGGGACTATAGGTGCGTACCACCATGCCTG A T RBBP4 Ensembl:ENSG00000162521 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1447290364 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_43959 31070 RMVar_ID_31070 Human_SNP_ID_8602275 A-to-I Human chr1 + 32673577 32673577 32673577 CTCCTGCCTCAGCCTTCTGAGTAGCTGGGACTATAGGTGCGTACCACCATGCCTGGCTAATTTTT CTCCTGCCTCAGCCTTCTGAGTAGCTGGGACTGTAGGTGCGTACCACCATGCCTGGCTAATTTTT A G RBBP4 Ensembl:ENSG00000162521 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs960839900 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_43959 31071 RMVar_ID_31071 Human_SNP_ID_8602349 A-to-I Human chr1 + 32673843 32673843 32673843 ATATTCGGCCGAGCACGTTGGCTCACGCCTGTAATCCCAGTACTCTGGGAGGCCGAGGCGGGTGG ATATTCGGCCGAGCACGTTGGCTCACGCCTGTGATCCCAGTACTCTGGGAGGCCGAGGCGGGTGG A G RBBP4 Ensembl:ENSG00000162521 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs980054556 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24685896 31072 RMVar_ID_31072 Human_SNP_ID_8602512 A-to-I Human chr1 + 32674351 32674351 32674351 CAATTCCCGGGCTCAAGACATCCTCCTACCTCAGCCTCCCTAGTAACTGGGACCACAGGTGTGCA CAATTCCCGGGCTCAAGACATCCTCCTACCTCGGCCTCCCTAGTAACTGGGACCACAGGTGTGCA A G RBBP4 Ensembl:ENSG00000162521 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1245438802 Functional Loss SNV dbSNP153 33..33 33 - - - 31073 RMVar_ID_31073 Human_SNP_ID_8602535 A-to-I Human chr1 + 32674434 32674434 32674434 TTTTAAAATTTTTTGTAGAGATGGGGTTTGCCATGTTGGCCAGTCTGGTCTTGAACTTGTGAGCT TTTTAAAATTTTTTGTAGAGATGGGGTTTGCCTTGTTGGCCAGTCTGGTCTTGAACTTGTGAGCT A T RBBP4 Ensembl:ENSG00000162521 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1271137159 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10945822,Human_RBP_ID_17557110 31074 RMVar_ID_31074 Human_SNP_ID_8602548 A-to-I Human chr1 + 32674468 32674468 32674468 GTTGGCCAGTCTGGTCTTGAACTTGTGAGCTCAAGCGATTTGCCCACCTCCCAGAGTGCTGGGAG GTTGGCCAGTCTGGTCTTGAACTTGTGAGCTCCAGCGATTTGCCCACCTCCCAGAGTGCTGGGAG A C RBBP4 Ensembl:ENSG00000162521 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs564825077 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5812472,Human_RBP_ID_10945823,Human_RBP_ID_18572359 31075 RMVar_ID_31075 Human_SNP_ID_8602549 A-to-I Human chr1 + 32674468 32674468 32674468 GTTGGCCAGTCTGGTCTTGAACTTGTGAGCTCAAGCGATTTGCCCACCTCCCAGAGTGCTGGGAG GTTGGCCAGTCTGGTCTTGAACTTGTGAGCTCGAGCGATTTGCCCACCTCCCAGAGTGCTGGGAG A G RBBP4 Ensembl:ENSG00000162521 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs564825077 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5812472,Human_RBP_ID_10945823,Human_RBP_ID_18572359 31076 RMVar_ID_31076 Human_SNP_ID_8602573 A-to-I Human chr1 + 32674531 32674531 32674531 AGTACATGTGTGAGGCTGCCCACCCGCCCCCCACTTTTTTTTGTTTTTAAAGAAGTGCGTAACTT AGTACATGTGTGAGGCTGCCCACCCGCCCCCCCCTTTTTTTTGTTTTTAAAGAAGTGCGTAACTT A C RBBP4 Ensembl:ENSG00000162521 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6681759 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10945829 31077 RMVar_ID_31077 Human_SNP_ID_8602574 A-to-I Human chr1 + 32674531 32674531 32674531 AGTACATGTGTGAGGCTGCCCACCCGCCCCCCACTTTTTTTTGTTTTTAAAGAAGTGCGTAACTT AGTACATGTGTGAGGCTGCCCACCCGCCCCCCGCTTTTTTTTGTTTTTAAAGAAGTGCGTAACTT A G RBBP4 Ensembl:ENSG00000162521 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6681759 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10945829 31078 RMVar_ID_31078 Human_SNP_ID_8602665 A-to-I Human chr1 + 32674861 32674861 32674861 GCAATTCTCCTGCCTCAGCCTGCTGATTAGCTAGGATTACAGGCATGCACCACCATGCCCGGCTA GCAATTCTCCTGCCTCAGCCTGCTGATTAGCTGGGATTACAGGCATGCACCACCATGCCCGGCTA A G RBBP4 Ensembl:ENSG00000162521 Protein coding intron GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs1227705344 Functional Loss SNV dbSNP153 33..33 33 - - - 31079 RMVar_ID_31079 Human_SNP_ID_8602709 A-to-I Human chr1 + 32674973 32674973 32674973 GTTGGTCAGGGTGGTCTCGATCTCCTGACCTCATGATCCGCCCTCTTTGGCCTCCCAAAGTACTG GTTGGTCAGGGTGGTCTCGATCTCCTGACCTCCTGATCCGCCCTCTTTGGCCTCCCAAAGTACTG A C RBBP4 Ensembl:ENSG00000162521 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1336017005 Functional Loss SNV dbSNP153 33..33 33 - - - 31080 RMVar_ID_31080 Human_SNP_ID_8602739 A-to-I Human chr1 + 32675067 32675067 32675067 CATTTTTATTTTTGAGACGGAGTTTTGTTCTTATTTTCCAGCCTGGAGTGCAATGGTGCGATCTT CATTTTTATTTTTGAGACGGAGTTTTGTTCTTCTTTTCCAGCCTGGAGTGCAATGGTGCGATCTT A C RBBP4 Ensembl:ENSG00000162521 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs12138418 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10945849 31081 RMVar_ID_31081 Human_SNP_ID_8602740 A-to-I Human chr1 + 32675067 32675067 32675067 CATTTTTATTTTTGAGACGGAGTTTTGTTCTTATTTTCCAGCCTGGAGTGCAATGGTGCGATCTT CATTTTTATTTTTGAGACGGAGTTTTGTTCTTGTTTTCCAGCCTGGAGTGCAATGGTGCGATCTT A G RBBP4 Ensembl:ENSG00000162521 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs12138418 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10945849 31082 RMVar_ID_31082 Human_SNP_ID_8602741 A-to-I Human chr1 + 32675086 32675086 32675086 GAGTTTTGTTCTTATTTTCCAGCCTGGAGTGCAATGGTGCGATCTTGGCTCTCTGCAACCTCCGC GAGTTTTGTTCTTATTTTCCAGCCTGGAGTGCGATGGTGCGATCTTGGCTCTCTGCAACCTCCGC A G RBBP4 Ensembl:ENSG00000162521 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1222366415 Functional Loss SNV dbSNP153 33..33 33 - - - 31083 RMVar_ID_31083 Human_SNP_ID_8602785 A-to-I Human chr1 + 32675216 32675216 32675216 CCACGCCTGGCTAAATTTTTGTAATTTTTTTTAGTAGAGACTGGGTTTCTCCATGTTGGTCAGGC CCACGCCTGGCTAAATTTTTGTAATTTTTTTTGGTAGAGACTGGGTTTCTCCATGTTGGTCAGGC A G RBBP4 Ensembl:ENSG00000162521 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1423556653 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10945851 31084 RMVar_ID_31084 Human_SNP_ID_8603067 A-to-I Human chr1 + 32676100 32676100 32676100 GGGAGGCCGTGACAGAAGGATCCCTTGAGGCCAGGAGTTTGAGGCTACAGTGGGCTGTGATCACA GGGAGGCCGTGACAGAAGGATCCCTTGAGGCCTGGAGTTTGAGGCTACAGTGGGCTGTGATCACA A T RBBP4 Ensembl:ENSG00000162521 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1253859454 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10945883,Human_RBP_ID_17557789 31085 RMVar_ID_31085 Human_SNP_ID_8603171 A-to-I Human chr1 + 32676561 32676560 32676561 GAACCCAGGAGGCGGAGGAGTTGCGGTGAGCCAAGATCGCACCATTGCACTCGAACATGGGCAAC GAACCCAGGAGGCGGAGGAGTTGCGGTGAGCC_AGATCGCACCATTGCACTCGAACATGGGCAAC CA C RBBP4 Ensembl:ENSG00000162521 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs760939610 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_10945906,Human_RBP_ID_17557790,Human_RBP_ID_24685956 31086 RMVar_ID_31086 Human_SNP_ID_8603736 A-to-I Human chr1 + 32678326 32678326 32678326 TTGGCTCACTGCAACCTCCGCCTCCTGGGTTCAAGCGATTCTCCTGCCTTAGCCTCCCAAATAGC TTGGCTCACTGCAACCTCCGCCTCCTGGGTTCGAGCGATTCTCCTGCCTTAGCCTCCCAAATAGC A G RBBP4 Ensembl:ENSG00000162521 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs973579126 Functional Loss SNV dbSNP153 33..33 33 - - - 31087 RMVar_ID_31087 Human_SNP_ID_8603887 A-to-I Human chr1 + 32678667 32678667 32678667 GCTGGAGTGCAGTGGTGCAATCTTGGCTCACTACAACCACCACCTCCCAGGTTCAATCAATTCTT GCTGGAGTGCAGTGGTGCAATCTTGGCTCACTGCAACCACCACCTCCCAGGTTCAATCAATTCTT A G RBBP4 Ensembl:ENSG00000162521 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs188031582 Functional Loss SNV dbSNP153 33..33 33 - - - 31088 RMVar_ID_31088 Human_SNP_ID_8603926 A-to-I Human chr1 + 32678824 32678824 32678824 GTTGGTCAGGCTAGTCTCAAACTCATGACCTCAAGTGATCTGTCTGCCTCAGCCTCCCAAGTGCT GTTGGTCAGGCTAGTCTCAAACTCATGACCTCCAGTGATCTGTCTGCCTCAGCCTCCCAAGTGCT A C RBBP4 Ensembl:ENSG00000162521 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs769748964 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1255209,Human_RBP_ID_10946014 31089 RMVar_ID_31089 Human_SNP_ID_8603969 A-to-I Human chr1 + 32679039 32679039 32679039 TCTGGTTAGGCTGGGCACAATGGCTTACTCCTATAATCCTAGCACTTTGAGAGGCCGAGGTGGGC TCTGGTTAGGCTGGGCACAATGGCTTACTCCTGTAATCCTAGCACTTTGAGAGGCCGAGGTGGGC A G RBBP4 Ensembl:ENSG00000162521 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1461698037 Functional Loss SNV dbSNP153 33..33 33 - - - 31090 RMVar_ID_31090 Human_SNP_ID_8604013 A-to-I Human chr1 + 32679160 32679160 32679160 CTCTATTAAAAATACAAAAATTAGCCAGGCGTAGTGGCATGTGCCTGTAATCCTAGCTACTCTGG CTCTATTAAAAATACAAAAATTAGCCAGGCGTGGTGGCATGTGCCTGTAATCCTAGCTACTCTGG A G RBBP4 Ensembl:ENSG00000162521 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1290222882 Functional Loss SNV dbSNP153 33..33 33 - - - 31091 RMVar_ID_31091 Human_SNP_ID_8604258 A-to-I Human chr1 - 32680133 32680133 32680133 AAGATTTTCGAGTAGGAATCTATATGACTTGAATCTCCCCCTATTTCCTGAATAAAAGTGACATC AAGATTTTCGAGTAGGAATCTATATGACTTGAGTCTCCCCCTATTTCCTGAATAAAAGTGACATC T C SYNC Ensembl:ENSG00000162520 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs555426509 Functional Loss SNV dbSNP153 33..33 33 - - - 31092 RMVar_ID_31092 Human_SNP_ID_8604911 A-to-I Human chr1 + 32682523 32682519 32682524 GGCCAGGCGCGGTGGTTCACGCCTGTAATCCCAGCACTTTGAGAGGCTGAGGCACGTGGATCACA GGCCAGGCGCGGTGGTTCACGCCTGTAAT_____CACTTTGAGAGGCTGAGGCACGTGGATCACA TCCCAG T RBBP4 Ensembl:ENSG00000162521 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1488056090 Functional Loss DEL dbSNP153 30..34 33 - - - Human_RBP_ID_352817,Human_RBP_ID_10946229 31093 RMVar_ID_31093 Human_SNP_ID_8604913 A-to-I Human chr1 + 32682523 32682523 32682523 GGCCAGGCGCGGTGGTTCACGCCTGTAATCCCAGCACTTTGAGAGGCTGAGGCACGTGGATCACA GGCCAGGCGCGGTGGTTCACGCCTGTAATCCCTGCACTTTGAGAGGCTGAGGCACGTGGATCACA A T RBBP4 Ensembl:ENSG00000162521 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs921189812 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_352817,Human_RBP_ID_10946229 31094 RMVar_ID_31094 Human_SNP_ID_8604931 A-to-I Human chr1 + 32682609 32682608 32682609 CCTGGCCAAGATGGTGAAACCCCGTTTCTACTAAAAATACAAAAACTAGCTGGCCGTGGTGGCAT CCTGGCCAAGATGGTGAAACCCCGTTTCTACT_AAAATACAAAAACTAGCTGGCCGTGGTGGCAT TA T RBBP4 Ensembl:ENSG00000162521 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1367520391 Functional Loss DEL dbSNP153 33..33 33 - - - 31095 RMVar_ID_31095 Human_SNP_ID_8604932 A-to-I Human chr1 + 32682609 32682609 32682609 CCTGGCCAAGATGGTGAAACCCCGTTTCTACTAAAAATACAAAAACTAGCTGGCCGTGGTGGCAT CCTGGCCAAGATGGTGAAACCCCGTTTCTACTCAAAATACAAAAACTAGCTGGCCGTGGTGGCAT A C RBBP4 Ensembl:ENSG00000162521 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1230476096 Functional Loss SNV dbSNP153 33..33 33 - - - 31096 RMVar_ID_31096 Human_SNP_ID_8605042 A-to-I Human chr1 + 32683022 32683022 32683022 TAAGTCTGTTTAGGCCAAGCATGGTGGCTCACACCTGAAATCCCAGCACTCTGGGAGGCCGAGGC TAAGTCTGTTTAGGCCAAGCATGGTGGCTCACGCCTGAAATCCCAGCACTCTGGGAGGCCGAGGC A G RBBP4 Ensembl:ENSG00000162521 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1062305 Functional Loss SNV dbSNP153 33..33 33 - - - 31097 RMVar_ID_31097 Human_SNP_ID_8605045 A-to-I Human chr1 + 32683034 32683034 32683034 GGCCAAGCATGGTGGCTCACACCTGAAATCCCAGCACTCTGGGAGGCCGAGGCAAGTGGATCACA GGCCAAGCATGGTGGCTCACACCTGAAATCCCGGCACTCTGGGAGGCCGAGGCAAGTGGATCACA A G RBBP4 Ensembl:ENSG00000162521 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1142597 Functional Loss SNV dbSNP153 33..33 33 - - - 31098 RMVar_ID_31098 Human_SNP_ID_8605066 A-to-I Human chr1 + 32683090 32683090 32683090 TGGATCACAAGGTCAGGAGATGAGACCATCTTAGCCAACATGGTGAAACCCCGTCTCTACTAAAA TGGATCACAAGGTCAGGAGATGAGACCATCTTGGCCAACATGGTGAAACCCCGTCTCTACTAAAA A G RBBP4 Ensembl:ENSG00000162521 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs3179729 Functional Loss SNV dbSNP153 33..33 33 - - - 31099 RMVar_ID_31099 Human_SNP_ID_8605076 A-to-I Human chr1 + 32683119 32683119 32683119 CTTAGCCAACATGGTGAAACCCCGTCTCTACTAAAATACAAAAAAATTAGCCAGGCGTGGTGGTG CTTAGCCAACATGGTGAAACCCCGTCTCTACTGAAATACAAAAAAATTAGCCAGGCGTGGTGGTG A G RBBP4 Ensembl:ENSG00000162521 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1189076125 Functional Loss SNV dbSNP153 33..33 33 - - - 31100 RMVar_ID_31100 Human_SNP_ID_8605081 A-to-I Human chr1 + 32683135 32683135 32683135 AAACCCCGTCTCTACTAAAATACAAAAAAATTAGCCAGGCGTGGTGGTGCGTGCCTATAATCCCA AAACCCCGTCTCTACTAAAATACAAAAAAATTGGCCAGGCGTGGTGGTGCGTGCCTATAATCCCA A G RBBP4 Ensembl:ENSG00000162521 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs3180044 Functional Loss SNV dbSNP153 33..33 33 - - - 31101 RMVar_ID_31101 Human_SNP_ID_8605113 A-to-I Human chr1 + 32683247 32683246 32683248 GAGGTCACGCCACTGCACTCCAGCCTGGCAACAGAGCAAGACTCCGTCTCAAAAAAAAAAAAAAA GAGGTCACGCCACTGCACTCCAGCCTGGCAAC__AGCAAGACTCCGTCTCAAAAAAAAAAAAAAA CAG C RBBP4 Ensembl:ENSG00000162521 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1487459532 Functional Loss DEL dbSNP153 33..34 33 - - - 31102 RMVar_ID_31102 Human_SNP_ID_8605236 A-to-I Human chr1 + 32683665 32683661 32683665 TTTGGGTTTTTGTTTTGTTTTGAGGCAGTCTCACTCTGTTGTACAAGCTGGAGTGCTGTATTGTG TTTGGGTTTTTGTTTTGTTTTGAGGCAGT____CTCTGTTGTACAAGCTGGAGTGCTGTATTGTG TCTCA T RBBP4 Ensembl:ENSG00000162521 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs779357877 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_5812586,Human_RBP_ID_10946277,Human_RBP_ID_17557112,Human_RBP_ID_26387901 31103 RMVar_ID_31103 Human_SNP_ID_8605257 A-to-I Human chr1 + 32683737 32683737 32683737 CTCACTGCAACCTCTGCCTCCTGGTTCAAGCGATTCTCCTGCCTTGGCCTCCTGAGTAGCTGGGA CTCACTGCAACCTCTGCCTCCTGGTTCAAGCGGTTCTCCTGCCTTGGCCTCCTGAGTAGCTGGGA A G RBBP4 Ensembl:ENSG00000162521 Protein coding 3'UTR GSE38233;GSE107867;GSE107867 cultured B-cells;ASD brains,cerebellum;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 24183664,30559470,30559470 RNA-Seq:(High) rs924893274 Functional Loss SNV dbSNP153 33..33 33 - - - 31104 RMVar_ID_31104 Human_SNP_ID_8605265 A-to-I Human chr1 + 32683772 32683772 32683772 CTCCTGCCTTGGCCTCCTGAGTAGCTGGGATTATAAGTGCCTGCCACTATGCCCGGCTAATTTTT CTCCTGCCTTGGCCTCCTGAGTAGCTGGGATTGTAAGTGCCTGCCACTATGCCCGGCTAATTTTT A G RBBP4 Ensembl:ENSG00000162521 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 23474544,24183664,29129909,31158229 RNA-Seq:(High) rs545280403 Functional Loss SNV dbSNP153 33..33 33 - - - 31105 RMVar_ID_31105 Human_SNP_ID_8605396 A-to-I Human chr1 - 32684160 32684158 32684160 GAAAATTTTACCTTAGAATCAAAAACAAAAAGAGGATTTGGGAAATGATTTTCAAATTGTGCTTA GAAAATTTTACCTTAGAATCAAAAACAAAAAG__GATTTGGGAAATGATTTTCAAATTGTGCTTA CCT C SYNC Ensembl:ENSG00000162520 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1423705144 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_24496,RMVar_hsa_circ_303761,RMVar_hsa_circ_131282,RMVar_hsa_circ_131283 31106 RMVar_ID_31106 Human_SNP_ID_8605714 A-to-I Human chr1 + 32685084 32685084 32685084 ATGTTGCCCAGGCTGGTCTTGTTCCTGGGCTCAAGCAGTCCTCCCGCCTCGGTCTCCCAAAGTGC ATGTTGCCCAGGCTGGTCTTGTTCCTGGGCTCGAGCAGTCCTCCCGCCTCGGTCTCCCAAAGTGC A G RBBP4 Ensembl:ENSG00000162521 Protein coding 3'UTR GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1408496298 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10946342 31107 RMVar_ID_31107 Human_SNP_ID_8606667 A-to-I Human chr1 - 32687988 32687988 32687988 TCTACTAAAAATACAAAAATTAGGCCGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGACAGGAGA TCTACTAAAAATACAAAAATTAGGCCGCCTGTGGTCCCAGCTACTTGGGAGGCTGAGACAGGAGA T C SYNC Ensembl:ENSG00000162520 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1403857934 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37438,RMVar_hsa_circ_24496 31108 RMVar_ID_31108 Human_SNP_ID_8608390 A-to-I Human chr1 - 32694071 32694071 32694071 GTGTGTGCCACCATACCTGGCTAATTTTTTGTAGAGACAGGGTTTCACCACGTGGCCCAGGCTGG GTGTGTGCCACCATACCTGGCTAATTTTTTGTGGAGACAGGGTTTCACCACGTGGCCCAGGCTGG T C SYNC Ensembl:ENSG00000162520 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1452532588 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37438,RMVar_hsa_circ_24496 31109 RMVar_ID_31109 Human_SNP_ID_8621557 A-to-I Human chr1 + 32745032 32745032 32745032 CCTGTAGTCCCAGCTACCCGGAAGGCTGAGGCAAGAGAATTGCTTGAACTCGGGAGGCGGAGGTT CCTGTAGTCCCAGCTACCCGGAAGGCTGAGGCTAGAGAATTGCTTGAACTCGGGAGGCGGAGGTT A T KIAA1522 Ensembl:ENSG00000162522 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991430989 Functional Loss SNV dbSNP153 33..33 33 - - - 31110 RMVar_ID_31110 Human_SNP_ID_8630100 A-to-I Human chr1 - 32776000 32776000 32776000 CAAGCTGGGCTCCATTTCCTGTAAATCGCTGAAAGGGGGGAACATTAGCTAGCCAGCCCAGCATC CAAGCTGGGCTCCATTTCCTGTAAATCGCTGATAGGGGGGAACATTAGCTAGCCAGCCCAGCATC T A YARS1 Ensembl:ENSG00000134684 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1221215452 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_352930,Human_RBP_ID_1348202,Human_RBP_ID_1429574,Human_RBP_ID_5812669,Human_RBP_ID_8308734,Human_RBP_ID_17218114,Human_RBP_ID_17335416,Human_RBP_ID_17749101,Human_RBP_ID_18229436,Human_RBP_ID_18572419,Human_RBP_ID_22025899,Human_RBP_ID_26862798 Human_Splice_Rec_44060,Human_Splice_Rec_44084,Human_Splice_Rec_44086,Human_Splice_Rec_44094,Human_Splice_Rec_44104 RMVar_hsa_circ_97767,RMVar_hsa_circ_116445,RMVar_hsa_circ_125184,RMVar_hsa_circ_106365,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_131285 31111 RMVar_ID_31111 Human_SNP_ID_8630299 A-to-I Human chr1 - 32776777 32776777 32776777 TAATTTTAGTAGAGACGGGGTTTCACTGTATTAGCCAGGATGGTCTCAATCTCCTGACCTCGTGA TAATTTTAGTAGAGACGGGGTTTCACTGTATTGGCCAGGATGGTCTCAATCTCCTGACCTCGTGA T C YARS1 Ensembl:ENSG00000134684 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs964709352 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97767,RMVar_hsa_circ_116445,RMVar_hsa_circ_125184,RMVar_hsa_circ_106365,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_131285 31112 RMVar_ID_31112 Human_SNP_ID_8630544 A-to-I Human chr1 - 32777774 32777774 32777774 AATTAGAAACAGGGTCTCACTCTTGTCACCCAAGCTGGATTCCAGTGGTGCCATCATAGCTCCCT AATTAGAAACAGGGTCTCACTCTTGTCACCCACGCTGGATTCCAGTGGTGCCATCATAGCTCCCT T G YARS1 Ensembl:ENSG00000134684 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956011570 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97767,RMVar_hsa_circ_116445,RMVar_hsa_circ_125184,RMVar_hsa_circ_106365,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_131285 31113 RMVar_ID_31113 Human_SNP_ID_8632693 A-to-I Human chr1 - 32786138 32786138 32786138 GTTAGCTTTTCTGACTTAGGAATTTTGTTAATACAGATGGATTTCTATCCCTCGGGGCCCTTTCC GTTAGCTTTTCTGACTTAGGAATTTTGTTAATGCAGATGGATTTCTATCCCTCGGGGCCCTTTCC T C YARS1 Ensembl:ENSG00000134684 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs785415 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_3490,GWAS_ID_3491,GWAS_ID_3492 RMVar_hsa_circ_97767,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_331832,RMVar_hsa_circ_43532,RMVar_hsa_circ_327940 31114 RMVar_ID_31114 Human_SNP_ID_8633004 A-to-I Human chr1 - 32787286 32787286 32787286 CCTGTCTCTACAAAAAATAGAATTACCTGGGCATGGTGACACATTCCTGTAGTCCCAGCTTTCCA CCTGTCTCTACAAAAAATAGAATTACCTGGGCTTGGTGACACATTCCTGTAGTCCCAGCTTTCCA T A YARS1 Ensembl:ENSG00000134684 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs785416 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_3493,GWAS_ID_3494,GWAS_ID_3495 RMVar_hsa_circ_106365,RMVar_hsa_circ_89944,RMVar_hsa_circ_131290,RMVar_hsa_circ_80528,RMVar_hsa_circ_131291,RMVar_hsa_circ_131289,RMVar_hsa_circ_331832,RMVar_hsa_circ_4360,RMVar_hsa_circ_43532,RMVar_hsa_circ_308132,RMVar_hsa_circ_374232,RMVar_hsa_circ_327940,RMVar_hsa_circ_299243,RMVar_hsa_circ_131296,RMVar_hsa_circ_131297,RMVar_hsa_circ_131295 31115 RMVar_ID_31115 Human_SNP_ID_8633005 A-to-I Human chr1 - 32787286 32787286 32787286 CCTGTCTCTACAAAAAATAGAATTACCTGGGCATGGTGACACATTCCTGTAGTCCCAGCTTTCCA CCTGTCTCTACAAAAAATAGAATTACCTGGGCGTGGTGACACATTCCTGTAGTCCCAGCTTTCCA T C YARS1 Ensembl:ENSG00000134684 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs785416 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_3493,GWAS_ID_3494,GWAS_ID_3495 RMVar_hsa_circ_106365,RMVar_hsa_circ_89944,RMVar_hsa_circ_131290,RMVar_hsa_circ_80528,RMVar_hsa_circ_131291,RMVar_hsa_circ_131289,RMVar_hsa_circ_331832,RMVar_hsa_circ_4360,RMVar_hsa_circ_43532,RMVar_hsa_circ_308132,RMVar_hsa_circ_374232,RMVar_hsa_circ_327940,RMVar_hsa_circ_299243,RMVar_hsa_circ_131296,RMVar_hsa_circ_131297,RMVar_hsa_circ_131295 31116 RMVar_ID_31116 Human_SNP_ID_8633095 A-to-I Human chr1 - 32787647 32787646 32787647 AAATTAGCTGGGCGTGGTGACAGGCACCTGTAATCCCAGCTATTCGGGAGGCTGAGGCGGGAGAA AAATTAGCTGGGCGTGGTGACAGGCACCTGTA_TCCCAGCTATTCGGGAGGCTGAGGCGGGAGAA AT A YARS1 Ensembl:ENSG00000134684 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1322395432 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_106365,RMVar_hsa_circ_89944,RMVar_hsa_circ_131290,RMVar_hsa_circ_80528,RMVar_hsa_circ_131291,RMVar_hsa_circ_131289,RMVar_hsa_circ_331832,RMVar_hsa_circ_4360,RMVar_hsa_circ_43532,RMVar_hsa_circ_308132,RMVar_hsa_circ_374232,RMVar_hsa_circ_327940,RMVar_hsa_circ_299243,RMVar_hsa_circ_131296,RMVar_hsa_circ_131297,RMVar_hsa_circ_131295 31117 RMVar_ID_31117 Human_SNP_ID_8633200 A-to-I Human chr1 - 32788027 32788027 32788027 CATGCCTCACTGCACTTTCAACCTCAGGCTCAAGTGATCCTCCTGCCTCAGCCTCCTGAGTAGCT CATGCCTCACTGCACTTTCAACCTCAGGCTCATGTGATCCTCCTGCCTCAGCCTCCTGAGTAGCT T A YARS1 Ensembl:ENSG00000134684 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1301945364 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106365,RMVar_hsa_circ_89944,RMVar_hsa_circ_131290,RMVar_hsa_circ_80528,RMVar_hsa_circ_131291,RMVar_hsa_circ_131289,RMVar_hsa_circ_331832,RMVar_hsa_circ_4360,RMVar_hsa_circ_43532,RMVar_hsa_circ_308132,RMVar_hsa_circ_374232,RMVar_hsa_circ_327940,RMVar_hsa_circ_299243,RMVar_hsa_circ_131296,RMVar_hsa_circ_131297,RMVar_hsa_circ_131295 31118 RMVar_ID_31118 Human_SNP_ID_8633656 A-to-I Human chr1 - 32789946 32789928 32789946 CCAGGAGGCAGAGGTTGCAGTGAGCCAAGATCACACTGTTGCACTCCAGCCTGGGCAACAAGAGC CCAGGAGGCAGAGGTTGCAGTGAGCCAAGATC__________________CTGGGCAACAAGAGC GGCTGGAGTGCAACAGTGT G YARS1 Ensembl:ENSG00000134684 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs748255750 Functional Loss DEL dbSNP153 33..50 33 - - - RMVar_hsa_circ_106365,RMVar_hsa_circ_89944,RMVar_hsa_circ_131290,RMVar_hsa_circ_80528,RMVar_hsa_circ_131291,RMVar_hsa_circ_131289,RMVar_hsa_circ_331832,RMVar_hsa_circ_4360,RMVar_hsa_circ_43532,RMVar_hsa_circ_308132,RMVar_hsa_circ_374232,RMVar_hsa_circ_327940,RMVar_hsa_circ_299243,RMVar_hsa_circ_131296,RMVar_hsa_circ_131297,RMVar_hsa_circ_131295 31119 RMVar_ID_31119 Human_SNP_ID_8634471 A-to-I Human chr1 - 32793249 32793249 32793249 GTTTTCATCAAATTTGGGAAATTGTCTGCCATAATTTCCTCAAATACTGCTTCTCTCTTATTCTC GTTTTCATCAAATTTGGGAAATTGTCTGCCATTATTTCCTCAAATACTGCTTCTCTCTTATTCTC T A YARS1 Ensembl:ENSG00000134684 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6425801 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19343384 GWAS_ID_3496,GWAS_ID_3497,GWAS_ID_3498 RMVar_hsa_circ_89944,RMVar_hsa_circ_131290,RMVar_hsa_circ_80528,RMVar_hsa_circ_131291,RMVar_hsa_circ_4360,RMVar_hsa_circ_43532,RMVar_hsa_circ_308132,RMVar_hsa_circ_374232,RMVar_hsa_circ_38899,RMVar_hsa_circ_131296,RMVar_hsa_circ_330715,RMVar_hsa_circ_131295,RMVar_hsa_circ_307378,RMVar_hsa_circ_131298 31120 RMVar_ID_31120 Human_SNP_ID_8634472 A-to-I Human chr1 - 32793249 32793249 32793249 GTTTTCATCAAATTTGGGAAATTGTCTGCCATAATTTCCTCAAATACTGCTTCTCTCTTATTCTC GTTTTCATCAAATTTGGGAAATTGTCTGCCATGATTTCCTCAAATACTGCTTCTCTCTTATTCTC T C YARS1 Ensembl:ENSG00000134684 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6425801 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19343384 GWAS_ID_3496,GWAS_ID_3497,GWAS_ID_3498 RMVar_hsa_circ_89944,RMVar_hsa_circ_131290,RMVar_hsa_circ_80528,RMVar_hsa_circ_131291,RMVar_hsa_circ_4360,RMVar_hsa_circ_43532,RMVar_hsa_circ_308132,RMVar_hsa_circ_374232,RMVar_hsa_circ_38899,RMVar_hsa_circ_131296,RMVar_hsa_circ_330715,RMVar_hsa_circ_131295,RMVar_hsa_circ_307378,RMVar_hsa_circ_131298 31121 RMVar_ID_31121 Human_SNP_ID_8634689 A-to-I Human chr1 - 32794331 32794331 32794331 TTTTTAATTTTTCTGAGACTGAGTCTCCCTCTATCACCCAGGCTGAAGGGCAGCGGCATGATCTC TTTTTAATTTTTCTGAGACTGAGTCTCCCTCTGTCACCCAGGCTGAAGGGCAGCGGCATGATCTC T C YARS1 Ensembl:ENSG00000134684 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs933831869 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10947143,Human_RBP_ID_19449575,Human_RBP_ID_23149060 RMVar_hsa_circ_89944,RMVar_hsa_circ_131290,RMVar_hsa_circ_80528,RMVar_hsa_circ_131291,RMVar_hsa_circ_4360,RMVar_hsa_circ_43532,RMVar_hsa_circ_308132,RMVar_hsa_circ_374232,RMVar_hsa_circ_38899,RMVar_hsa_circ_131296,RMVar_hsa_circ_330715,RMVar_hsa_circ_131295,RMVar_hsa_circ_307378,RMVar_hsa_circ_131298 31122 RMVar_ID_31122 Human_SNP_ID_8634693 A-to-I Human chr1 - 32794342 32794342 32794342 CTACCATTTTTTTTTTAATTTTTCTGAGACTGAGTCTCCCTCTATCACCCAGGCTGAAGGGCAGC CTACCATTTTTTTTTTAATTTTTCTGAGACTGTGTCTCCCTCTATCACCCAGGCTGAAGGGCAGC T A YARS1 Ensembl:ENSG00000134684 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs889716456 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10947143,Human_RBP_ID_18572459 RMVar_hsa_circ_89944,RMVar_hsa_circ_131290,RMVar_hsa_circ_80528,RMVar_hsa_circ_131291,RMVar_hsa_circ_4360,RMVar_hsa_circ_43532,RMVar_hsa_circ_308132,RMVar_hsa_circ_374232,RMVar_hsa_circ_38899,RMVar_hsa_circ_131296,RMVar_hsa_circ_330715,RMVar_hsa_circ_131295,RMVar_hsa_circ_307378,RMVar_hsa_circ_131298 31123 RMVar_ID_31123 Human_SNP_ID_8634739 A-to-I Human chr1 - 32794530 32794530 32794530 CAAAAATTAGCCAGACGCAGTGGTGTGCACCTATAATCCCAGCTATTCAAGAGGCTGACACAGGA CAAAAATTAGCCAGACGCAGTGGTGTGCACCTGTAATCCCAGCTATTCAAGAGGCTGACACAGGA T C YARS1 Ensembl:ENSG00000134684 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs966778106 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89944,RMVar_hsa_circ_131290,RMVar_hsa_circ_80528,RMVar_hsa_circ_131291,RMVar_hsa_circ_4360,RMVar_hsa_circ_43532,RMVar_hsa_circ_308132,RMVar_hsa_circ_374232,RMVar_hsa_circ_38899,RMVar_hsa_circ_131296,RMVar_hsa_circ_330715,RMVar_hsa_circ_131295,RMVar_hsa_circ_307378,RMVar_hsa_circ_131298 31124 RMVar_ID_31124 Human_SNP_ID_8634745 A-to-I Human chr1 - 32794550 32794550 32794550 CCCCGTCTCTAGTAAAAATACAAAAATTAGCCAGACGCAGTGGTGTGCACCTATAATCCCAGCTA CCCCGTCTCTAGTAAAAATACAAAAATTAGCCGGACGCAGTGGTGTGCACCTATAATCCCAGCTA T C YARS1 Ensembl:ENSG00000134684 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs971655950 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89944,RMVar_hsa_circ_131290,RMVar_hsa_circ_80528,RMVar_hsa_circ_131291,RMVar_hsa_circ_4360,RMVar_hsa_circ_43532,RMVar_hsa_circ_308132,RMVar_hsa_circ_374232,RMVar_hsa_circ_38899,RMVar_hsa_circ_131296,RMVar_hsa_circ_330715,RMVar_hsa_circ_131295,RMVar_hsa_circ_307378,RMVar_hsa_circ_131298 31125 RMVar_ID_31125 Human_SNP_ID_8634933 A-to-I Human chr1 - 32795154 32795154 32795154 CCACCACACCCTGCTAATTTTTTGTATTTTTAATAGAGACGGGGTTTCACCGTGTTAGCCAAGGT CCACCACACCCTGCTAATTTTTTGTATTTTTATTAGAGACGGGGTTTCACCGTGTTAGCCAAGGT T A YARS1 Ensembl:ENSG00000134684 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1765231 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_3499,GWAS_ID_3500,GWAS_ID_3501 RMVar_hsa_circ_89944,RMVar_hsa_circ_131290,RMVar_hsa_circ_80528,RMVar_hsa_circ_131291,RMVar_hsa_circ_4360,RMVar_hsa_circ_43532,RMVar_hsa_circ_308132,RMVar_hsa_circ_374232,RMVar_hsa_circ_38899,RMVar_hsa_circ_131296,RMVar_hsa_circ_330715,RMVar_hsa_circ_131295,RMVar_hsa_circ_307378,RMVar_hsa_circ_131298 31126 RMVar_ID_31126 Human_SNP_ID_8634934 A-to-I Human chr1 - 32795154 32795154 32795154 CCACCACACCCTGCTAATTTTTTGTATTTTTAATAGAGACGGGGTTTCACCGTGTTAGCCAAGGT CCACCACACCCTGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAAGGT T C YARS1 Ensembl:ENSG00000134684 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1765231 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_3499,GWAS_ID_3500,GWAS_ID_3501 RMVar_hsa_circ_89944,RMVar_hsa_circ_131290,RMVar_hsa_circ_80528,RMVar_hsa_circ_131291,RMVar_hsa_circ_4360,RMVar_hsa_circ_43532,RMVar_hsa_circ_308132,RMVar_hsa_circ_374232,RMVar_hsa_circ_38899,RMVar_hsa_circ_131296,RMVar_hsa_circ_330715,RMVar_hsa_circ_131295,RMVar_hsa_circ_307378,RMVar_hsa_circ_131298 31127 RMVar_ID_31127 Human_SNP_ID_8639034 A-to-I Human chr1 - 32810049 32810049 32810049 CAGGCTGGAGTGCAATGGCGCGATCTTGACTCACTGCACCCTCTGCCTCCTGGGTTCAAGAGATT CAGGCTGGAGTGCAATGGCGCGATCTTGACTCGCTGCACCCTCTGCCTCCTGGGTTCAAGAGATT T C YARS1 Ensembl:ENSG00000134684 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1175270848 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89944,RMVar_hsa_circ_131290,RMVar_hsa_circ_80528,RMVar_hsa_circ_131291,RMVar_hsa_circ_95078,RMVar_hsa_circ_4360,RMVar_hsa_circ_374232,RMVar_hsa_circ_131295,RMVar_hsa_circ_307378,RMVar_hsa_circ_354237,RMVar_hsa_circ_131300,RMVar_hsa_circ_127104,RMVar_hsa_circ_323742,RMVar_hsa_circ_131302,RMVar_hsa_circ_131303 31128 RMVar_ID_31128 Human_SNP_ID_8639643 A-to-I Human chr1 - 32812288 32812288 32812288 CAGAGGATCACCAGGTGGGGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGACTAAGGCCAGA CAGAGGATCACCAGGTGGGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGACTAAGGCCAGA T C YARS1 Ensembl:ENSG00000134684 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs576047168 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80528,RMVar_hsa_circ_131291,RMVar_hsa_circ_95078,RMVar_hsa_circ_131300 31129 RMVar_ID_31129 Human_SNP_ID_8639759 A-to-I Human chr1 - 32812805 32812805 32812805 TGCCACCATGCCCTGCTAATTTTTGTATTTTTAGTAGAGATGGTTTCACCATGTTGGCCAGGCTG TGCCACCATGCCCTGCTAATTTTTGTATTTTTGGTAGAGATGGTTTCACCATGTTGGCCAGGCTG T C YARS1 Ensembl:ENSG00000134684 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs893536303 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80528,RMVar_hsa_circ_131291,RMVar_hsa_circ_95078,RMVar_hsa_circ_131300 31130 RMVar_ID_31130 Human_SNP_ID_8639926 A-to-I Human chr1 - 32813439 32813439 32813439 TGTTGGACGCCTGTAATCTCAGCTACTCTGGAAGCTGAGGCAGGAGAATCACTTGAACCCTGGAG TGTTGGACGCCTGTAATCTCAGCTACTCTGGAGGCTGAGGCAGGAGAATCACTTGAACCCTGGAG T C YARS1 Ensembl:ENSG00000134684 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1319729589 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80528,RMVar_hsa_circ_131291,RMVar_hsa_circ_95078,RMVar_hsa_circ_131300 31131 RMVar_ID_31131 Human_SNP_ID_8640153 A-to-I Human chr1 - 32814495 32814495 32814495 ATTCCAGCTATTTGGGAGACTGAAGCAGGAGAATCGTTTGAACCCGGGAGCAGAGGTTGCAGTGA ATTCCAGCTATTTGGGAGACTGAAGCAGGAGAGTCGTTTGAACCCGGGAGCAGAGGTTGCAGTGA T C YARS1 Ensembl:ENSG00000134684 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1233419962 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10947779 RMVar_hsa_circ_80528,RMVar_hsa_circ_131291,RMVar_hsa_circ_95078,RMVar_hsa_circ_131300 31132 RMVar_ID_31132 Human_SNP_ID_8640173 A-to-I Human chr1 - 32814593 32814593 32814593 TTGAGGTTGGGAGTTCAAGACCAGCCTGGCCAACATAGTGAAACCCCATCTCTACTAAAAATACA TTGAGGTTGGGAGTTCAAGACCAGCCTGGCCAGCATAGTGAAACCCCATCTCTACTAAAAATACA T C YARS1 Ensembl:ENSG00000134684 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs182315375 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80528,RMVar_hsa_circ_131291,RMVar_hsa_circ_95078,RMVar_hsa_circ_131300 31133 RMVar_ID_31133 Human_SNP_ID_8640193 A-to-I Human chr1 - 32814656 32814656 32814656 GCCAAGCGCAGTGGCTCATGCCGGTAATCCCAACACTTTGGGAGGCCCACACGGGCAGATCACTT GCCAAGCGCAGTGGCTCATGCCGGTAATCCCAGCACTTTGGGAGGCCCACACGGGCAGATCACTT T C YARS1 Ensembl:ENSG00000134684 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs554924765 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80528,RMVar_hsa_circ_131291,RMVar_hsa_circ_95078,RMVar_hsa_circ_131300 31134 RMVar_ID_31134 Human_SNP_ID_8641501 A-to-I Human chr1 + 32819290 32819290 32819290 TATTCTTCCCTTAAAAATGAAGGGATATGGCCAGACATGGTGGCTCACGCCTGTAATCCCAGCAC TATTCTTCCCTTAAAAATGAAGGGATATGGCCGGACATGGTGGCTCACGCCTGTAATCCCAGCAC A G S100PBP Ensembl:ENSG00000116497 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs563376707 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90137,RMVar_hsa_circ_131305 31135 RMVar_ID_31135 Human_SNP_ID_8641516 A-to-I Human chr1 + 32819358 32819358 32819358 GGGAGGCCGAGGCCGGAGGATTGCTTGAGGCCAGGAGTTCAAGACTAGACTGGCCAACATAGCAA GGGAGGCCGAGGCCGGAGGATTGCTTGAGGCCCGGAGTTCAAGACTAGACTGGCCAACATAGCAA A C S100PBP Ensembl:ENSG00000116497 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1209640585 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90137,RMVar_hsa_circ_131305 31136 RMVar_ID_31136 Human_SNP_ID_8641526 A-to-I Human chr1 + 32819397 32819397 32819397 CAAGACTAGACTGGCCAACATAGCAAAACCCCATCTCTACTGTAAATACAAAAATTAGCCTAGCA CAAGACTAGACTGGCCAACATAGCAAAACCCCGTCTCTACTGTAAATACAAAAATTAGCCTAGCA A G S100PBP Ensembl:ENSG00000116497 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1471331510 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90137,RMVar_hsa_circ_131305 31137 RMVar_ID_31137 Human_SNP_ID_8641808 A-to-I Human chr1 + 32820420 32820420 32820420 CACCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGAATCAGCCTCTGCGCCTGGCCCTATGCT CACCCACCTCAGCCTCCCAAAGTGCTGGGATTGCAGGAATCAGCCTCTGCGCCTGGCCCTATGCT A G S100PBP Ensembl:ENSG00000116497 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1015530193 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10947961 RMVar_hsa_circ_90137,RMVar_hsa_circ_131305 31138 RMVar_ID_31138 Human_SNP_ID_8642214 A-to-I Human chr1 + 32821839 32821839 32821839 CTTTGTAGTTTTAGTAGAAATGGGGTTCCGCCATGTTGGTCAGGCTGGTCTCGAACTCCTGGCCT CTTTGTAGTTTTAGTAGAAATGGGGTTCCGCCCTGTTGGTCAGGCTGGTCTCGAACTCCTGGCCT A C S100PBP Ensembl:ENSG00000116497 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs181831627 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10948014 RMVar_hsa_circ_90137,RMVar_hsa_circ_131305 31139 RMVar_ID_31139 Human_SNP_ID_8644669 A-to-I Human chr1 + 32830957 32830957 32830957 AAAAAATTAGCCAGGCGTGGTGGCACATGCCTATAATCCTAGCTACTCAGGTGGCTGAGGCACAA AAAAAATTAGCCAGGCGTGGTGGCACATGCCTGTAATCCTAGCTACTCAGGTGGCTGAGGCACAA A G S100PBP Ensembl:ENSG00000116497 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs991678572 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90137,RMVar_hsa_circ_131305,RMVar_hsa_circ_46069,RMVar_hsa_circ_273527,RMVar_hsa_circ_131307,RMVar_hsa_circ_17462 31140 RMVar_ID_31140 Human_SNP_ID_8645568 A-to-I Human chr1 + 32834978 32834978 32834978 GCCTGACTAACATGATGAAACCTGTCTCTACTAAAAATATAAAAATTAGCTGGGCGTGGTGGTGG GCCTGACTAACATGATGAAACCTGTCTCTACTGAAAATATAAAAATTAGCTGGGCGTGGTGGTGG A G S100PBP Ensembl:ENSG00000116497 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs773053157 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90137,RMVar_hsa_circ_131305,RMVar_hsa_circ_273527,RMVar_hsa_circ_131307,RMVar_hsa_circ_17462 31141 RMVar_ID_31141 Human_SNP_ID_8645595 A-to-I Human chr1 + 32835065 32835065 32835065 GGGAGGCTGAGGCAGGAGAATCTCTTGAACCCAAGAGGCAGAAGTTGTAGTGAGCGAAGATCAGG GGGAGGCTGAGGCAGGAGAATCTCTTGAACCCGAGAGGCAGAAGTTGTAGTGAGCGAAGATCAGG A G S100PBP Ensembl:ENSG00000116497 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs918360983 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10948234 RMVar_hsa_circ_90137,RMVar_hsa_circ_131305,RMVar_hsa_circ_273527,RMVar_hsa_circ_131307,RMVar_hsa_circ_17462 31142 RMVar_ID_31142 Human_SNP_ID_8646040 A-to-I Human chr1 + 32837027 32837027 32837027 TTGGGAGGCTGAGGTGGGCGGATCCCAAGGTCAAGAGTTCGAGACCAGTCTGGCCAATATGGTGA TTGGGAGGCTGAGGTGGGCGGATCCCAAGGTCGAGAGTTCGAGACCAGTCTGGCCAATATGGTGA A G S100PBP Ensembl:ENSG00000116497 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1158837330 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24764320 RMVar_hsa_circ_90137,RMVar_hsa_circ_131305,RMVar_hsa_circ_273527,RMVar_hsa_circ_131307,RMVar_hsa_circ_17462 31143 RMVar_ID_31143 Human_SNP_ID_8646170 A-to-I Human chr1 + 32837379 32837379 32837379 GTAATCTGAGCTCACTGCAGCCTCCACCTCCCAGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCTA GTAATCTGAGCTCACTGCAGCCTCCACCTCCCGGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCTA A G S100PBP Ensembl:ENSG00000116497 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs890186233 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90137,RMVar_hsa_circ_131305,RMVar_hsa_circ_273527,RMVar_hsa_circ_131307,RMVar_hsa_circ_17462 31144 RMVar_ID_31144 Human_SNP_ID_8646346 A-to-I Human chr1 + 32838095 32838095 32838095 TGGGTGCGGTGGCTCACGCCTGTAATCCCAGCACTTTTGGAGGCCGAGGCGGGCGGATCACGAGG TGGGTGCGGTGGCTCACGCCTGTAATCCCAGCCCTTTTGGAGGCCGAGGCGGGCGGATCACGAGG A C S100PBP Ensembl:ENSG00000116497 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs964107381 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_96163,Human_RBP_ID_24686609 RMVar_hsa_circ_90137,RMVar_hsa_circ_131305,RMVar_hsa_circ_273527,RMVar_hsa_circ_131307,RMVar_hsa_circ_17462 31145 RMVar_ID_31145 Human_SNP_ID_8646921 A-to-I Human chr1 + 32840169 32840169 32840169 CACCATATCCGGCTAATTTTTGTATTTTTAGTAGAGGTGGGGTTTTACCATGTTGGCCAGGCTGG CACCATATCCGGCTAATTTTTGTATTTTTAGTGGAGGTGGGGTTTTACCATGTTGGCCAGGCTGG A G S100PBP Ensembl:ENSG00000116497 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1040938632 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90137,RMVar_hsa_circ_131305,RMVar_hsa_circ_273527,RMVar_hsa_circ_131307,RMVar_hsa_circ_17462 31146 RMVar_ID_31146 Human_SNP_ID_8646992 A-to-I Human chr1 + 32840474 32840474 32840474 CCCTCCTGGGTTCAAGCAATTCTCCCTGCCTCAGTCTCCCAAGTAGCTGGGATTACAGGCACCCG CCCTCCTGGGTTCAAGCAATTCTCCCTGCCTCCGTCTCCCAAGTAGCTGGGATTACAGGCACCCG A C S100PBP Ensembl:ENSG00000116497 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1468666272 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90137,RMVar_hsa_circ_131305,RMVar_hsa_circ_273527,RMVar_hsa_circ_131307,RMVar_hsa_circ_17462 31147 RMVar_ID_31147 Human_SNP_ID_8647457 A-to-I Human chr1 + 32842090 32842090 32842090 ATACACCTGTAGTCCTTGCTACTCAGAAGGCTAAGGCAGGAGGATTGCTTAAGCCCAGAAGAGGG ATACACCTGTAGTCCTTGCTACTCAGAAGGCTGAGGCAGGAGGATTGCTTAAGCCCAGAAGAGGG A G S100PBP Ensembl:ENSG00000116497 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs902140479 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90137,RMVar_hsa_circ_131305,RMVar_hsa_circ_273527,RMVar_hsa_circ_131307,RMVar_hsa_circ_17462 31148 RMVar_ID_31148 Human_SNP_ID_8647735 A-to-I Human chr1 + 32842626 32842622 32842626 CATTTTATTTTATTTTTTTGAGATGGAGTCTCACTCTGTTGCCTAGGCTGTCGTGCGGTGGTGCG CATTTTATTTTATTTTTTTGAGATGGAGT____CTCTGTTGCCTAGGCTGTCGTGCGGTGGTGCG TCTCA T S100PBP Ensembl:ENSG00000116497 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs995749995 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_10948353 RMVar_hsa_circ_90137,RMVar_hsa_circ_131305,RMVar_hsa_circ_273527,RMVar_hsa_circ_131307,RMVar_hsa_circ_17462 31149 RMVar_ID_31149 Human_SNP_ID_8647736 A-to-I Human chr1 + 32842626 32842626 32842626 CATTTTATTTTATTTTTTTGAGATGGAGTCTCACTCTGTTGCCTAGGCTGTCGTGCGGTGGTGCG CATTTTATTTTATTTTTTTGAGATGGAGTCTCGCTCTGTTGCCTAGGCTGTCGTGCGGTGGTGCG A G S100PBP Ensembl:ENSG00000116497 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1025516049 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10948353 RMVar_hsa_circ_90137,RMVar_hsa_circ_131305,RMVar_hsa_circ_273527,RMVar_hsa_circ_131307,RMVar_hsa_circ_17462 31150 RMVar_ID_31150 Human_SNP_ID_8648452 A-to-I Human chr1 + 32845240 32845240 32845240 TAGAGACGGGGTTTCACCACGTTAGCTGTGTTAGCCAGGATGGTCTCGATCTCCTGGCCTTTCTT TAGAGACGGGGTTTCACCACGTTAGCTGTGTTGGCCAGGATGGTCTCGATCTCCTGGCCTTTCTT A G S100PBP Ensembl:ENSG00000116497 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs909851178 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90137,RMVar_hsa_circ_131305,RMVar_hsa_circ_273527,RMVar_hsa_circ_131307,RMVar_hsa_circ_17462 31151 RMVar_ID_31151 Human_SNP_ID_8648490 A-to-I Human chr1 + 32845385 32845385 32845385 GGAACCCTTGAACCCAGGAGGCTGAGTGAACCAATGTCGTGTCACGGCACTCCAGCCTAGGTGAC GGAACCCTTGAACCCAGGAGGCTGAGTGAACCGATGTCGTGTCACGGCACTCCAGCCTAGGTGAC A G S100PBP Ensembl:ENSG00000116497 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1251921572 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24764344 RMVar_hsa_circ_90137,RMVar_hsa_circ_131305,RMVar_hsa_circ_273527,RMVar_hsa_circ_131307,RMVar_hsa_circ_17462 31152 RMVar_ID_31152 Human_SNP_ID_8648534 A-to-I Human chr1 + 32845525 32845525 32845525 TCTTGGCCTCCCAAAGTGCCACAATTACAGGCATGAGTCACCATGCCTGGCCTTGTTTTCTAGCT TCTTGGCCTCCCAAAGTGCCACAATTACAGGCGTGAGTCACCATGCCTGGCCTTGTTTTCTAGCT A G S100PBP Ensembl:ENSG00000116497 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs980405791 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90137,RMVar_hsa_circ_131305,RMVar_hsa_circ_273527,RMVar_hsa_circ_131307,RMVar_hsa_circ_17462 31153 RMVar_ID_31153 Human_SNP_ID_8648582 A-to-I Human chr1 + 32845699 32845698 32845699 GATATGTTTTCATTTTCTTTTTTTTTTTTTTTAAGATAAAGCCTTGCTCTGTCACCCAGCCTGAG GATATGTTTTCATTTTCTTTTTTTTTTTTTTT_AGATAAAGCCTTGCTCTGTCACCCAGCCTGAG TA T S100PBP Ensembl:ENSG00000116497 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1483138293 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5909065,Human_RBP_ID_10948415,Human_RBP_ID_23149115 RMVar_hsa_circ_90137,RMVar_hsa_circ_131305,RMVar_hsa_circ_273527,RMVar_hsa_circ_131307,RMVar_hsa_circ_17462 31154 RMVar_ID_31154 Human_SNP_ID_8648584 A-to-I Human chr1 + 32845699 32845699 32845699 GATATGTTTTCATTTTCTTTTTTTTTTTTTTTAAGATAAAGCCTTGCTCTGTCACCCAGCCTGAG GATATGTTTTCATTTTCTTTTTTTTTTTTTTTTAGATAAAGCCTTGCTCTGTCACCCAGCCTGAG A T S100PBP Ensembl:ENSG00000116497 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1270114838 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5909065,Human_RBP_ID_10948415,Human_RBP_ID_23149115 RMVar_hsa_circ_90137,RMVar_hsa_circ_131305,RMVar_hsa_circ_273527,RMVar_hsa_circ_131307,RMVar_hsa_circ_17462 31155 RMVar_ID_31155 Human_SNP_ID_8674199 A-to-I Human chr1 + 32951459 32951459 32951459 GAGCCGGCGCACATGCAGGAGCCACCAGTGGCACAGGAGCAGTTGGGGTCCATTTCGAGCAAAGG GAGCCGGCGCACATGCAGGAGCCACCAGTGGCGCAGGAGCAGTTGGGGTCCATTTCGAGCAAAGG A G AL031602.2 Ensembl:ENSG00000287691 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941522778 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_44342 31156 RMVar_ID_31156 Human_SNP_ID_8674445 A-to-I Human chr1 - 32952392 32952392 32952392 AAAAGGTCTTGCTGTGTTGCCCAGGCTGGTCTAAAAATGCTGGCCTCAAGCGATCTTCCTGCCTC AAAAGGTCTTGCTGTGTTGCCCAGGCTGGTCTGAAAATGCTGGCCTCAAGCGATCTTCCTGCCTC T C RNF19B Ensembl:ENSG00000116514 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1026039787 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24686822 RMVar_hsa_circ_103360,RMVar_hsa_circ_131322 31157 RMVar_ID_31157 Human_SNP_ID_8674446 A-to-I Human chr1 - 32952392 32952392 32952392 AAAAGGTCTTGCTGTGTTGCCCAGGCTGGTCTAAAAATGCTGGCCTCAAGCGATCTTCCTGCCTC AAAAGGTCTTGCTGTGTTGCCCAGGCTGGTCTCAAAATGCTGGCCTCAAGCGATCTTCCTGCCTC T G RNF19B Ensembl:ENSG00000116514 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1026039787 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24686822 RMVar_hsa_circ_103360,RMVar_hsa_circ_131322 31158 RMVar_ID_31158 Human_SNP_ID_8674607 A-to-I Human chr1 - 32952773 32952773 32952773 AAGTAGCTGTGACTGCAGGCCTGTGTCACCATACCTGGCTGATTTTTTTTTTTTTTTGAGATGGA AAGTAGCTGTGACTGCAGGCCTGTGTCACCATCCCTGGCTGATTTTTTTTTTTTTTTGAGATGGA T G RNF19B Ensembl:ENSG00000116514 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1424217295 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103360,RMVar_hsa_circ_131322 31159 RMVar_ID_31159 Human_SNP_ID_8682629 A-to-I Human chr1 - 32982501 32982501 32982501 TTGTTGTTGTTTTTGAGACAAAGTCTTGCTCTATCACTAGGGTGGAGCGCAGTGGTGCGATCTCG TTGTTGTTGTTTTTGAGACAAAGTCTTGCTCTGTCACTAGGGTGGAGCGCAGTGGTGCGATCTCG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs566239477 Functional Loss SNV dbSNP153 33..33 33 - - - 31160 RMVar_ID_31160 Human_SNP_ID_8684072 A-to-I Human chr1 - 32988527 32988527 32988527 TAAAAACTCCGTTGACCGGGGCAGTGGCTCACACCTGTAATCTTAGCACTTTGGGAGGCCGAGGC TAAAAACTCCGTTGACCGGGGCAGTGGCTCACGCCTGTAATCTTAGCACTTTGGGAGGCCGAGGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1007396534 Functional Loss SNV dbSNP153 33..33 33 - - - 31161 RMVar_ID_31161 Human_SNP_ID_8693902 A-to-I Human chr1 - 33026358 33026358 33026358 TAAGAAAACTCCCAATTACATAAAAATTAGCCAGGCACGTGGCTTGTGCCTGCAATCCCAGCTAC TAAGAAAACTCCCAATTACATAAAAATTAGCCGGGCACGTGGCTTGTGCCTGCAATCCCAGCTAC T C AK2 Ensembl:ENSG00000004455 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1349826102 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114354,RMVar_hsa_circ_131326,RMVar_hsa_circ_33935,RMVar_hsa_circ_309607 31162 RMVar_ID_31162 Human_SNP_ID_8803047 A-to-I Human chr1 + 33484881 33484881 33484881 TGACTTGGTGATCTGCCTGCCTTGGCCTCTCAAAGTGCTGGTATTACAGGTCTGAGCCACCACAC TGACTTGGTGATCTGCCTGCCTTGGCCTCTCACAGTGCTGGTATTACAGGTCTGAGCCACCACAC A C ZSCAN20 Ensembl:ENSG00000121903 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1383061583 Functional Loss SNV dbSNP153 33..33 33 - - - 31163 RMVar_ID_31163 Human_SNP_ID_9164263 A-to-I Human chr1 - 34982614 34982614 34982614 ACATTAGCCGGGCGTGGTGGTGCGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAA ACATTAGCCGGGCGTGGTGGTGCGCGCCTGTATTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAA T A TMEM35B,AC114490.2,AC114490.3 Ensembl:ENSG00000243749,Ensembl:ENSG00000271741,Ensembl:ENSG00000284773 Protein coding,Protein coding,Protein coding intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs890163084 Functional Loss SNV dbSNP153 33..33 33 - - - 31164 RMVar_ID_31164 Human_SNP_ID_9164264 A-to-I Human chr1 - 34982614 34982614 34982614 ACATTAGCCGGGCGTGGTGGTGCGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAA ACATTAGCCGGGCGTGGTGGTGCGCGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAA T C TMEM35B,AC114490.2,AC114490.3 Ensembl:ENSG00000243749,Ensembl:ENSG00000271741,Ensembl:ENSG00000284773 Protein coding,Protein coding,Protein coding intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs890163084 Functional Loss SNV dbSNP153 33..33 33 - - - 31165 RMVar_ID_31165 Human_SNP_ID_9164466 A-to-I Human chr1 - 34983457 34983457 34983457 CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCTGCCACAGCGCCCGACTGATTTTT CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTGCAGGCGCCTGCCACAGCGCCCGACTGATTTTT T C TMEM35B,AC114490.2,AC114490.3 Ensembl:ENSG00000243749,Ensembl:ENSG00000271741,Ensembl:ENSG00000284773 Protein coding,Protein coding,Protein coding intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs955811967 Functional Loss SNV dbSNP153 33..33 33 - - - 31166 RMVar_ID_31166 Human_SNP_ID_9166648 A-to-I Human chr1 - 34991729 34991729 34991729 TTTCACTCTTGTTGCCCAGGCTGGAGTGCAATAGCGTGATCTTGGCTCCCTATAACCTCTGCCTC TTTCACTCTTGTTGCCCAGGCTGGAGTGCAATGGCGTGATCTTGGCTCCCTATAACCTCTGCCTC T C ZMYM6,AC114490.2 Ensembl:ENSG00000163867,Ensembl:ENSG00000271741 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs550424041 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8116,RMVar_hsa_circ_99106,RMVar_hsa_circ_131412 31167 RMVar_ID_31167 Human_SNP_ID_9173242 A-to-I Human chr1 + 35018892 35018892 35018892 GCTGTTTTTTCCTCTCTCTGCATCTAAGCATTATTGTAAAGCAACAATGACCCCACAAGGACATT GCTGTTTTTTCCTCTCTCTGCATCTAAGCATTGTTGTAAAGCAACAATGACCCCACAAGGACATT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917936298 Functional Loss SNV dbSNP153 33..33 33 - - - 31168 RMVar_ID_31168 Human_SNP_ID_9188627 A-to-I Human chr1 - 35084718 35084718 35084718 AGTGAGACTTCAAAAACTTAACAGAACACAGCAGTTAAACGTCAAAGAGCTAATAAGATTATAGC AGTGAGACTTCAAAAACTTAACAGAACACAGCGGTTAAACGTCAAAGAGCTAATAAGATTATAGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs373999156 Functional Loss SNV dbSNP153 33..33 33 - - - 31169 RMVar_ID_31169 Human_SNP_ID_9190633 A-to-I Human chr1 + 35091989 35091989 35091989 GCTCTGTCTCCCAGGCTGGAGTGCAATGGCACAATCTTGGCTGACTGCAACCTCTGCCTCCCGTT GCTCTGTCTCCCAGGCTGGAGTGCAATGGCACGATCTTGGCTGACTGCAACCTCTGCCTCCCGTT A G ZMYM1 Ensembl:ENSG00000197056 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1442657243 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113633,RMVar_hsa_circ_131421 31170 RMVar_ID_31170 Human_SNP_ID_9191916 A-to-I Human chr1 + 35096896 35096896 35096896 TAATTTTTATAGTAGAGACGGGGTTTCACCATATTGCCCGGGATGGTCTCAATCTCTTAAACTCG TAATTTTTATAGTAGAGACGGGGTTTCACCATGTTGCCCGGGATGGTCTCAATCTCTTAAACTCG A G ZMYM1 Ensembl:ENSG00000197056 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1431483715 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93263,RMVar_hsa_circ_77655,RMVar_hsa_circ_113633,RMVar_hsa_circ_131421,RMVar_hsa_circ_53395,RMVar_hsa_circ_284340,RMVar_hsa_circ_131422,RMVar_hsa_circ_275125,RMVar_hsa_circ_131424,RMVar_hsa_circ_131425,RMVar_hsa_circ_310691,RMVar_hsa_circ_131423,RMVar_hsa_circ_357609,RMVar_hsa_circ_293026,RMVar_hsa_circ_131427,RMVar_hsa_circ_131428,RMVar_hsa_circ_131429,RMVar_hsa_circ_131426 31171 RMVar_ID_31171 Human_SNP_ID_9192394 A-to-I Human chr1 + 35098692 35098690 35098692 ACTTAGGGAGGCCGAGGTGGGCAGAATGCCTGAGCTCAGGAGTTTGAGACCAGCCTGGCAACACA ACTTAGGGAGGCCGAGGTGGGCAGAATGCCT__GCTCAGGAGTTTGAGACCAGCCTGGCAACACA TGA T ZMYM1 Ensembl:ENSG00000197056 Protein coding intron GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs143113722 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_223087,Human_RBP_ID_744357 RMVar_hsa_circ_93263,RMVar_hsa_circ_113633,RMVar_hsa_circ_131421,RMVar_hsa_circ_284340,RMVar_hsa_circ_275125,RMVar_hsa_circ_131424,RMVar_hsa_circ_131425,RMVar_hsa_circ_310691,RMVar_hsa_circ_131423,RMVar_hsa_circ_357609,RMVar_hsa_circ_101394,RMVar_hsa_circ_131427,RMVar_hsa_circ_131428,RMVar_hsa_circ_131429,RMVar_hsa_circ_329642,RMVar_hsa_circ_275072,RMVar_hsa_circ_131430,RMVar_hsa_circ_131431,RMVar_hsa_circ_131432 31172 RMVar_ID_31172 Human_SNP_ID_9192796 A-to-I Human chr1 + 35100360 35100360 35100360 ATGCGATTTGTGGGCCAAGCGAGGTGGTTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGC ATGCGATTTGTGGGCCAAGCGAGGTGGTTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGC A G ZMYM1 Ensembl:ENSG00000197056 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1331942677 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1940848,Human_miRNA_ID_1943908,Human_miRNA_ID_2115039,Human_miRNA_ID_2198613,Human_miRNA_ID_2201683,Human_miRNA_ID_2314111,Human_miRNA_ID_2317271,Human_miRNA_ID_2320426,Human_miRNA_ID_2323580,Human_miRNA_ID_2517955,Human_miRNA_ID_2521133,Human_miRNA_ID_2773035,Human_miRNA_ID_2814150,Human_miRNA_ID_2820329,Human_miRNA_ID_2826463,Human_miRNA_ID_2829612,Human_miRNA_ID_2833734,Human_miRNA_ID_2839099,Human_miRNA_ID_2844285,Human_miRNA_ID_2847303,Human_miRNA_ID_2861409,Human_miRNA_ID_2889135,Human_miRNA_ID_3111136 RMVar_hsa_circ_93263,RMVar_hsa_circ_113633,RMVar_hsa_circ_131421,RMVar_hsa_circ_284340,RMVar_hsa_circ_275125,RMVar_hsa_circ_131424,RMVar_hsa_circ_131425,RMVar_hsa_circ_310691,RMVar_hsa_circ_131423,RMVar_hsa_circ_357609,RMVar_hsa_circ_101394,RMVar_hsa_circ_131428,RMVar_hsa_circ_131429,RMVar_hsa_circ_329642,RMVar_hsa_circ_275072,RMVar_hsa_circ_131433,RMVar_hsa_circ_131430,RMVar_hsa_circ_131431,RMVar_hsa_circ_131432,RMVar_hsa_circ_131434 31173 RMVar_ID_31173 Human_SNP_ID_9192930 A-to-I Human chr1 + 35100826 35100826 35100826 ATTTGTTGGCGTTTCTTTTTTTTTTTTGAGACAAGGTCCCTGTCTGTCACCCAGGTTGGAGTGCA ATTTGTTGGCGTTTCTTTTTTTTTTTTGAGACGAGGTCCCTGTCTGTCACCCAGGTTGGAGTGCA A G ZMYM1 Ensembl:ENSG00000197056 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1180458643 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_744101,Human_RBP_ID_2144457,Human_RBP_ID_10953730,Human_RBP_ID_26379513 RMVar_hsa_circ_93263,RMVar_hsa_circ_113633,RMVar_hsa_circ_131421,RMVar_hsa_circ_284340,RMVar_hsa_circ_275125,RMVar_hsa_circ_131424,RMVar_hsa_circ_131425,RMVar_hsa_circ_310691,RMVar_hsa_circ_131423,RMVar_hsa_circ_357609,RMVar_hsa_circ_101394,RMVar_hsa_circ_131428,RMVar_hsa_circ_131429,RMVar_hsa_circ_329642,RMVar_hsa_circ_275072,RMVar_hsa_circ_131433,RMVar_hsa_circ_131430,RMVar_hsa_circ_131431,RMVar_hsa_circ_131432,RMVar_hsa_circ_131434 31174 RMVar_ID_31174 Human_SNP_ID_9192946 A-to-I Human chr1 + 35100882 35100882 35100882 TGGAGTGCAGTGGCACCATCTTGGCTCACTGCAGCCTCGACCACCTGGGCTTAAGCAATACTCCC TGGAGTGCAGTGGCACCATCTTGGCTCACTGCGGCCTCGACCACCTGGGCTTAAGCAATACTCCC A G ZMYM1 Ensembl:ENSG00000197056 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1334347059 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10953734 RMVar_hsa_circ_93263,RMVar_hsa_circ_113633,RMVar_hsa_circ_131421,RMVar_hsa_circ_284340,RMVar_hsa_circ_275125,RMVar_hsa_circ_131424,RMVar_hsa_circ_131425,RMVar_hsa_circ_310691,RMVar_hsa_circ_131423,RMVar_hsa_circ_357609,RMVar_hsa_circ_101394,RMVar_hsa_circ_131428,RMVar_hsa_circ_131429,RMVar_hsa_circ_329642,RMVar_hsa_circ_275072,RMVar_hsa_circ_131433,RMVar_hsa_circ_131430,RMVar_hsa_circ_131431,RMVar_hsa_circ_131432,RMVar_hsa_circ_131434 31175 RMVar_ID_31175 Human_SNP_ID_9193196 A-to-I Human chr1 + 35101765 35101765 35101765 ATATTTTTAGTAGAGACGGGGTTGGCCAGGCTAGTCTCGAACTCCTGACCTCAAGTGATCTGCCC ATATTTTTAGTAGAGACGGGGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAAGTGATCTGCCC A G ZMYM1 Ensembl:ENSG00000197056 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1270580384 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10953768,Human_RBP_ID_17749530 RMVar_hsa_circ_284340,RMVar_hsa_circ_275125,RMVar_hsa_circ_131424,RMVar_hsa_circ_131425,RMVar_hsa_circ_310691,RMVar_hsa_circ_131423,RMVar_hsa_circ_357609,RMVar_hsa_circ_131429,RMVar_hsa_circ_329642,RMVar_hsa_circ_275072,RMVar_hsa_circ_131433,RMVar_hsa_circ_131431,RMVar_hsa_circ_131432,RMVar_hsa_circ_131434 31176 RMVar_ID_31176 Human_SNP_ID_9196976 A-to-I Human chr1 + 35115971 35115971 35115971 AGGTTGGGGACTGGGCGTGGTGGTTCACACCTATAATCTCAGCCCTTTGAGGGCCTACACAGGAA AGGTTGGGGACTGGGCGTGGTGGTTCACACCTGTAATCTCAGCCCTTTGAGGGCCTACACAGGAA A G RF00017-156 RNACentral:URS000091874B SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1396781538 Functional Loss SNV dbSNP153 33..33 33 - - - 31177 RMVar_ID_31177 Human_SNP_ID_9197163 A-to-I Human chr1 + 35116719 35116719 35116719 ACGTCAGGTAATACGCCCACCTGGGCCTCCCAAAGTGCTGGGATTATGGCATAAGCCACCACGCC ACGTCAGGTAATACGCCCACCTGGGCCTCCCAGAGTGCTGGGATTATGGCATAAGCCACCACGCC A G RF00017-156 RNACentral:URS000091874B SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1003746791 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23149184 31178 RMVar_ID_31178 Human_SNP_ID_9197169 A-to-I Human chr1 + 35116739 35116739 35116739 CTGGGCCTCCCAAAGTGCTGGGATTATGGCATAAGCCACCACGCCCAGCCAGAAAAGTTTAAATA CTGGGCCTCCCAAAGTGCTGGGATTATGGCATGAGCCACCACGCCCAGCCAGAAAAGTTTAAATA A G RF00017-156 RNACentral:URS000091874B SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1387172909 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23149184 31179 RMVar_ID_31179 Human_SNP_ID_9197517 A-to-I Human chr1 + 35117764 35117764 35117764 GGAGTTCAAGACCAGCCTGACTAACATGGAGAAACCCCGTCTCTACTAAAACTATAAAATTAGCC GGAGTTCAAGACCAGCCTGACTAACATGGAGACACCCCGTCTCTACTAAAACTATAAAATTAGCC A C RF00017-156 RNACentral:URS000091874B SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs891363898 Functional Loss SNV dbSNP153 33..33 33 - - - 31180 RMVar_ID_31180 Human_SNP_ID_9197518 A-to-I Human chr1 + 35117764 35117764 35117764 GGAGTTCAAGACCAGCCTGACTAACATGGAGAAACCCCGTCTCTACTAAAACTATAAAATTAGCC GGAGTTCAAGACCAGCCTGACTAACATGGAGAGACCCCGTCTCTACTAAAACTATAAAATTAGCC A G RF00017-156 RNACentral:URS000091874B SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs891363898 Functional Loss SNV dbSNP153 33..33 33 - - - 31181 RMVar_ID_31181 Human_SNP_ID_9197552 A-to-I Human chr1 + 35117919 35117919 35117919 CTGAGATCGTGCAATTGCACTCTAGTCTGGGCAACAAGAGAGAAACTCCGTTTCAAAAAAGAGAG CTGAGATCGTGCAATTGCACTCTAGTCTGGGCCACAAGAGAGAAACTCCGTTTCAAAAAAGAGAG A C RF00017-156 RNACentral:URS000091874B SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs574562492 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5814777 31182 RMVar_ID_31182 Human_SNP_ID_9197568 A-to-I Human chr1 + 35117982 35117982 35117982 AGAAAATAGGCTGGGGACGGTAGCTCACGCCTATAATCCCAACACTTTGGGAGGCTAAGGCAGGC AGAAAATAGGCTGGGGACGGTAGCTCACGCCTGTAATCCCAACACTTTGGGAGGCTAAGGCAGGC A G RF00017-156 RNACentral:URS000091874B SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs150958317 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4047172 31183 RMVar_ID_31183 Human_SNP_ID_9207762 A-to-I Human chr1 - 35157019 35157019 35157019 TGAGACAGAGTTTTGCTCTTGTCTCCCAGGCTAGAGTGCAGCTGCATGATCTCAGCTCACTGTAG TGAGACAGAGTTTTGCTCTTGTCTCCCAGGCTGGAGTGCAGCTGCATGATCTCAGCTCACTGTAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1424351903 Functional Loss SNV dbSNP153 33..33 33 - - - 31184 RMVar_ID_31184 Human_SNP_ID_9216642 A-to-I Human chr1 - 35188011 35188011 35188011 AACGTGAGATGGAAGAACAAATGAGGCGCCAAAGAGAGGAAAGTTACAGCCGAATGGGCTACATG AACGTGAGATGGAAGAACAAATGAGGCGCCAACGAGAGGAAAGTTACAGCCGAATGGGCTACATG T G SFPQ Ensembl:ENSG00000116560 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs200747734 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_802620,Human_RBP_ID_859584,Human_RBP_ID_1430171,Human_RBP_ID_1746242,Human_RBP_ID_3311103,Human_RBP_ID_4047363,Human_RBP_ID_5156090,Human_RBP_ID_5537738,Human_RBP_ID_5815393,Human_RBP_ID_8240782,Human_RBP_ID_9355983,Human_RBP_ID_10955015,Human_RBP_ID_17452641,Human_RBP_ID_18430213,Human_RBP_ID_18523190,Human_RBP_ID_18573041,Human_RBP_ID_18965198,Human_RBP_ID_21998785,Human_RBP_ID_22784720,Human_RBP_ID_22862748,Human_RBP_ID_23112418,Human_RBP_ID_23390489,Human_RBP_ID_24541065,Human_RBP_ID_26309713,Human_RBP_ID_26863429,Human_RBP_ID_27398080,Human_RBP_ID_27593802,Human_RBP_ID_27797767 Human_Splice_Rec_46285,Human_Splice_Rec_46300,Human_Splice_Rec_46301,Human_Splice_Rec_46346,Human_Splice_Rec_46347 RMVar_hsa_circ_131444,RMVar_hsa_circ_73151,RMVar_hsa_circ_300760,RMVar_hsa_circ_106327,RMVar_hsa_circ_131443,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_97765,RMVar_hsa_circ_131450,RMVar_hsa_circ_131451,RMVar_hsa_circ_63278,RMVar_hsa_circ_69466 31185 RMVar_ID_31185 Human_SNP_ID_9239814 A-to-I Human chr1 + 35270666 35270662 35270667 CCTGTAATCCCAGCTATTCGGGAGGCTGAGGCAGGGGAATCGCTTGAACCTGGGAGGCGGTGGTA CCTGTAATCCCAGCTATTCGGGAGGCTGA_____GGGAATCGCTTGAACCTGGGAGGCGGTGGTA AGGCAG A ZMYM4 Ensembl:ENSG00000146463 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1475661534 Functional Loss DEL dbSNP153 30..34 33 - - - 31186 RMVar_ID_31186 Human_SNP_ID_9254865 A-to-I Human chr1 + 35329828 35329828 35329828 CTCCTTCCACTGCCTCCCAAACTGCTAGGATTACCAGCATGAGTCACCACGCCCTACCCTTTAAA CTCCTTCCACTGCCTCCCAAACTGCTAGGATTGCCAGCATGAGTCACCACGCCCTACCCTTTAAA A G ZMYM4 Ensembl:ENSG00000146463 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs755030190 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3229,RMVar_hsa_circ_79146,RMVar_hsa_circ_46844,RMVar_hsa_circ_131456,RMVar_hsa_circ_131457,RMVar_hsa_circ_312877 31187 RMVar_ID_31187 Human_SNP_ID_9256236 A-to-I Human chr1 + 35335437 35335437 35335437 TTTTATATTTTTAGTAGAGACGAGGTTTCACCATGCTGGCAAGGCTGATCTCAAACTCCTGACCA TTTTATATTTTTAGTAGAGACGAGGTTTCACCGTGCTGGCAAGGCTGATCTCAAACTCCTGACCA A G ZMYM4 Ensembl:ENSG00000146463 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs76067984 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3229,RMVar_hsa_circ_79146,RMVar_hsa_circ_46844,RMVar_hsa_circ_131456,RMVar_hsa_circ_131457,RMVar_hsa_circ_312877 31188 RMVar_ID_31188 Human_SNP_ID_9273017 A-to-I Human chr1 + 35403389 35403389 35403389 CTCACTGTAACCTCCACCTTCCAGGTTCAAGCAGTTCTCCTGCCTCAGCCTTCCAAGTAGCTGGG CTCACTGTAACCTCCACCTTCCAGGTTCAAGCCGTTCTCCTGCCTCAGCCTTCCAAGTAGCTGGG A C ZMYM4 Ensembl:ENSG00000146463 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1355246309 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79146,RMVar_hsa_circ_131456,RMVar_hsa_circ_375313,RMVar_hsa_circ_57622,RMVar_hsa_circ_131459,RMVar_hsa_circ_73734,RMVar_hsa_circ_265557,RMVar_hsa_circ_58976,RMVar_hsa_circ_269107,RMVar_hsa_circ_328329,RMVar_hsa_circ_291756,RMVar_hsa_circ_286518,RMVar_hsa_circ_274574,RMVar_hsa_circ_131470,RMVar_hsa_circ_131472,RMVar_hsa_circ_131471,RMVar_hsa_circ_131469,RMVar_hsa_circ_131482,RMVar_hsa_circ_86421,RMVar_hsa_circ_359487,RMVar_hsa_circ_131496,RMVar_hsa_circ_131491,RMVar_hsa_circ_356262,RMVar_hsa_circ_364532,RMVar_hsa_circ_318311,RMVar_hsa_circ_131495,RMVar_hsa_circ_12045,RMVar_hsa_circ_269016,RMVar_hsa_circ_24224,RMVar_hsa_circ_41675,RMVar_hsa_circ_54089,RMVar_hsa_circ_131499,RMVar_hsa_circ_12322,RMVar_hsa_circ_378244,RMVar_hsa_circ_7376,RMVar_hsa_circ_49861 31189 RMVar_ID_31189 Human_SNP_ID_9288127 A-to-I Human chr1 - 35467890 35467890 35467890 GAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGGCAAAACCCATGTCTCTACTAAAAATAAAA GAGGTCAGGAGTTCAAGACCAGCCTGGCCAACCTGGCAAAACCCATGTCTCTACTAAAAATAAAA T G KIAA0319L Ensembl:ENSG00000142687 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1410560085 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8954,RMVar_hsa_circ_324505,RMVar_hsa_circ_33751,RMVar_hsa_circ_131516,RMVar_hsa_circ_125976,RMVar_hsa_circ_93663,RMVar_hsa_circ_131518,RMVar_hsa_circ_96180,RMVar_hsa_circ_131519,RMVar_hsa_circ_330727,RMVar_hsa_circ_25344,RMVar_hsa_circ_131520,RMVar_hsa_circ_311342,RMVar_hsa_circ_356318,RMVar_hsa_circ_131526,RMVar_hsa_circ_131523,RMVar_hsa_circ_131524,RMVar_hsa_circ_278902,RMVar_hsa_circ_333724,RMVar_hsa_circ_46848,RMVar_hsa_circ_324653,RMVar_hsa_circ_268206,RMVar_hsa_circ_131525 31190 RMVar_ID_31190 Human_SNP_ID_9292752 A-to-I Human chr1 - 35486679 35486679 35486679 GCAGGCTGATCTTGAACTTCTGGCCTTGAGCAATCCTCCCACCTTGGCCTCCCAGTATGCTAGGA GCAGGCTGATCTTGAACTTCTGGCCTTGAGCATTCCTCCCACCTTGGCCTCCCAGTATGCTAGGA T A KIAA0319L Ensembl:ENSG00000142687 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs983747695 Functional Loss SNV dbSNP153 33..33 33 - - - 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 31191 RMVar_ID_31191 Human_SNP_ID_9292753 A-to-I Human chr1 - 35486679 35486679 35486679 GCAGGCTGATCTTGAACTTCTGGCCTTGAGCAATCCTCCCACCTTGGCCTCCCAGTATGCTAGGA GCAGGCTGATCTTGAACTTCTGGCCTTGAGCAGTCCTCCCACCTTGGCCTCCCAGTATGCTAGGA T C KIAA0319L Ensembl:ENSG00000142687 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs983747695 Functional Loss SNV dbSNP153 33..33 33 - - - 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 31192 RMVar_ID_31192 Human_SNP_ID_9302417 A-to-I Human chr1 - 35526948 35526948 35526948 TCAGCCTGCTGAGTAGCTGGGACTATAGGTGCATGCTGCCATGCCTGAATAATTCTTTAAATTTT TCAGCCTGCTGAGTAGCTGGGACTATAGGTGCCTGCTGCCATGCCTGAATAATTCTTTAAATTTT T G KIAA0319L Ensembl:ENSG00000142687 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934440843 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96180,RMVar_hsa_circ_131519,RMVar_hsa_circ_268206 31193 RMVar_ID_31193 Human_SNP_ID_9302421 A-to-I Human chr1 - 35526956 35526956 35526956 CTCCCACCTCAGCCTGCTGAGTAGCTGGGACTATAGGTGCATGCTGCCATGCCTGAATAATTCTT CTCCCACCTCAGCCTGCTGAGTAGCTGGGACTGTAGGTGCATGCTGCCATGCCTGAATAATTCTT T C KIAA0319L Ensembl:ENSG00000142687 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1442730349 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96180,RMVar_hsa_circ_131519,RMVar_hsa_circ_268206 31194 RMVar_ID_31194 Human_SNP_ID_9307383 A-to-I Human chr1 - 35549113 35549113 35549113 CCGGGAGTTCAAGACTGCAGTGAACTGTGATCATGTCGCTGTACTCCAGTGTGGGTGACAGAGGG CCGGGAGTTCAAGACTGCAGTGAACTGTGATCGTGTCGCTGTACTCCAGTGTGGGTGACAGAGGG T C KIAA0319L Ensembl:ENSG00000142687 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1166117275 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96180,RMVar_hsa_circ_131519,RMVar_hsa_circ_268206 31195 RMVar_ID_31195 Human_SNP_ID_9307414 A-to-I Human chr1 - 35549227 35549227 35549227 CCTGGACAACATAGTGAAACCTCATCTCTACAAAAATAAAAAAAATTAGCTGGTGGTGGTGGGCA CCTGGACAACATAGTGAAACCTCATCTCTACAGAAATAAAAAAAATTAGCTGGTGGTGGTGGGCA T C KIAA0319L Ensembl:ENSG00000142687 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1449564000 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96180,RMVar_hsa_circ_131519,RMVar_hsa_circ_268206 31196 RMVar_ID_31196 Human_SNP_ID_9308109 A-to-I Human chr1 - 35552332 35552332 35552332 GACCAAAGGTTTTTTTTTTGAAACGGAGTCTCACTCTGTCACCAGGCTGGAGTGCAGTGGCGCAG GACCAAAGGTTTTTTTTTTGAAACGGAGTCTCGCTCTGTCACCAGGCTGGAGTGCAGTGGCGCAG T C KIAA0319L Ensembl:ENSG00000142687 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs759093992 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96180,RMVar_hsa_circ_131519,RMVar_hsa_circ_268206 31197 RMVar_ID_31197 Human_SNP_ID_9319633 A-to-I Human chr1 - 35598388 35598388 35598388 GACTAGGATGGTCTTGGAACCCCTGACCTCAAATGATCTGTCTGCCTCGGCTTCCCAAAGTGCTG GACTAGGATGGTCTTGGAACCCCTGACCTCAAGTGATCTGTCTGCCTCGGCTTCCCAAAGTGCTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1045738347 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10960844 31198 RMVar_ID_31198 Human_SNP_ID_9319982 A-to-I Human chr1 - 35599915 35599915 35599915 TTGCCTAGGCTGGTCTCGAACTCTTGGCCTCAAGTGATCCTCCCACCTTGGTCTGCCAAAGCACT TTGCCTAGGCTGGTCTCGAACTCTTGGCCTCAGGTGATCCTCCCACCTTGGTCTGCCAAAGCACT T C PSMB2 Ensembl:ENSG00000126067 Protein coding 3'UTR GSE38233;GSE100210;GSE112787;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;293 Flip-In T-REx cells,empty vector;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,29967493,31158229 RNA-Seq:(High) rs1415004059 Functional Loss SNV dbSNP153 33..33 33 - - - 31199 RMVar_ID_31199 Human_SNP_ID_9319986 A-to-I Human chr1 - 35599928 35599928 35599928 GGGTCTCGCCATGTTGCCTAGGCTGGTCTCGAACTCTTGGCCTCAAGTGATCCTCCCACCTTGGT GGGTCTCGCCATGTTGCCTAGGCTGGTCTCGAGCTCTTGGCCTCAAGTGATCCTCCCACCTTGGT T C PSMB2 Ensembl:ENSG00000126067 Protein coding 3'UTR GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,29796672,31158229,31158229,31158229 RNA-Seq:(High) rs1390169160 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26379609 31200 RMVar_ID_31200 Human_SNP_ID_9319989 A-to-I Human chr1 - 35599950 35599950 35599950 GTCAAAATTTTTTGTAGAGACAGGGTCTCGCCATGTTGCCTAGGCTGGTCTCGAACTCTTGGCCT GTCAAAATTTTTTGTAGAGACAGGGTCTCGCCGTGTTGCCTAGGCTGGTCTCGAACTCTTGGCCT T C PSMB2 Ensembl:ENSG00000126067 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs188046020 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17749825,Human_RBP_ID_24690485 31201 RMVar_ID_31201 Human_SNP_ID_9319994 A-to-I Human chr1 - 35599961 35599959 35599961 CAGCTAATTTTGTCAAAATTTTTTGTAGAGACAGGGTCTCGCCATGTTGCCTAGGCTGGTCTCGA CAGCTAATTTTGTCAAAATTTTTTGTAGAGAC__GGTCTCGCCATGTTGCCTAGGCTGGTCTCGA CCT C PSMB2 Ensembl:ENSG00000126067 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1285515890 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_17749825 31202 RMVar_ID_31202 Human_SNP_ID_9320000 A-to-I Human chr1 - 35599988 35599988 35599988 GGGACTAGAGGGGTGCACCACTGCACCCAGCTAATTTTGTCAAAATTTTTTGTAGAGACAGGGTC GGGACTAGAGGGGTGCACCACTGCACCCAGCTGATTTTGTCAAAATTTTTTGTAGAGACAGGGTC T C PSMB2 Ensembl:ENSG00000126067 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1044071174 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18229783,Human_RBP_ID_19349709 31203 RMVar_ID_31203 Human_SNP_ID_9320009 A-to-I Human chr1 - 35600053 35600053 35600053 CTGCAGTAAGTTCACTTGAACTCCTGGGCTCAAGTGAACCTCTTACCCCAGCCTCCCAACTAGCT CTGCAGTAAGTTCACTTGAACTCCTGGGCTCAGGTGAACCTCTTACCCCAGCCTCCCAACTAGCT T C PSMB2 Ensembl:ENSG00000126067 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs866331653 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3311477,Human_RBP_ID_17749826 31204 RMVar_ID_31204 Human_SNP_ID_9320010 A-to-I Human chr1 - 35600053 35600053 35600053 CTGCAGTAAGTTCACTTGAACTCCTGGGCTCAAGTGAACCTCTTACCCCAGCCTCCCAACTAGCT CTGCAGTAAGTTCACTTGAACTCCTGGGCTCACGTGAACCTCTTACCCCAGCCTCCCAACTAGCT T G PSMB2 Ensembl:ENSG00000126067 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs866331653 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3311477,Human_RBP_ID_17749826 31205 RMVar_ID_31205 Human_SNP_ID_9320018 A-to-I Human chr1 - 35600107 35600089 35600108 ACAGGGTCTTGCTCCATCACCTAGGCTGGAGTACAGTGGCACGATCGTAGCTTACTGCAGTAAGT ACAGGGTCTTGCTCCATCACCTAGGCTGGAG___________________CTTACTGCAGTAAGT GCTACGATCGTGCCACTGTA G PSMB2 Ensembl:ENSG00000126067 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229 RNA-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 31206 RMVar_ID_31206 Human_SNP_ID_9320255 A-to-I Human chr1 - 35601129 35601121 35601130 CCGGGAGAGGGAGGTTGCAGTGAGCCGAGATCATGCCACTGCACTCCAGCCTGGCTGACAGAGCA CCGGGAGAGGGAGGTTGCAGTGAGCCGAGAT_________GCACTCCAGCCTGGCTGACAGAGCA CAGTGGCATG C PSMB2 Ensembl:ENSG00000126067 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1326452320 Functional Loss DEL dbSNP153 32..40 33 - - - Human_RBP_ID_100941,Human_RBP_ID_24764979 31207 RMVar_ID_31207 Human_SNP_ID_9320256 A-to-I Human chr1 - 35601129 35601129 35601129 CCGGGAGAGGGAGGTTGCAGTGAGCCGAGATCATGCCACTGCACTCCAGCCTGGCTGACAGAGCA CCGGGAGAGGGAGGTTGCAGTGAGCCGAGATCGTGCCACTGCACTCCAGCCTGGCTGACAGAGCA T C PSMB2 Ensembl:ENSG00000126067 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1291428793 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_100941,Human_RBP_ID_24764979 31208 RMVar_ID_31208 Human_SNP_ID_9320296 A-to-I Human chr1 - 35601290 35601290 35601290 GAGGCGGGCGGATCACCTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCCCAT GAGGCGGGCGGATCACCTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCCAT T C PSMB2 Ensembl:ENSG00000126067 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs112880963 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_3502,GWAS_ID_3503 31209 RMVar_ID_31209 Human_SNP_ID_9320349 A-to-I Human chr1 - 35601421 35601421 35601421 ACCACCATGAATATGCATAGGTTTGAGCTTTTAGCTAGATTCCTGAGTGTAAGGCATCTATTTTA ACCACCATGAATATGCATAGGTTTGAGCTTTTGGCTAGATTCCTGAGTGTAAGGCATCTATTTTA T C PSMB2 Ensembl:ENSG00000126067 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1390189070 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10960932,Human_RBP_ID_17452704,Human_RBP_ID_18229793 31210 RMVar_ID_31210 Human_SNP_ID_9320499 A-to-I Human chr1 - 35602114 35602114 35602114 GTCATTCAGGTTGGTCTTGAACTCCTGGGCTCAAGCAGTCTGCCTGCCTTGGCTTCCCAGTGCTG GTCATTCAGGTTGGTCTTGAACTCCTGGGCTCGAGCAGTCTGCCTGCCTTGGCTTCCCAGTGCTG T C PSMB2 Ensembl:ENSG00000126067 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1471818489 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_353704,Human_RBP_ID_23149256,Human_RBP_ID_26379650 31211 RMVar_ID_31211 Human_SNP_ID_9320502 A-to-I Human chr1 - 35602148 35602148 35602148 TTTTGTGTTTTTCATAGAGACAGGGTCTCACCATGTCATTCAGGTTGGTCTTGAACTCCTGGGCT TTTTGTGTTTTTCATAGAGACAGGGTCTCACCGTGTCATTCAGGTTGGTCTTGAACTCCTGGGCT T C PSMB2 Ensembl:ENSG00000126067 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1132068 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_353704,Human_RBP_ID_8167941,Human_RBP_ID_26379653 31212 RMVar_ID_31212 Human_SNP_ID_9320505 A-to-I Human chr1 - 35602159 35602157 35602159 GCCCAGCTAGTTTTTGTGTTTTTCATAGAGACAGGGTCTCACCATGTCATTCAGGTTGGTCTTGA GCCCAGCTAGTTTTTGTGTTTTTCATAGAGAC__GGTCTCACCATGTCATTCAGGTTGGTCTTGA CCT C PSMB2 Ensembl:ENSG00000126067 Protein coding 3'UTR GSE100210;GSE112787 HepG2 cell line;293 Flip-In T-REx cells,empty vector - 29129909,29967493 RNA-Seq:(High) rs1429701307 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_353704,Human_RBP_ID_8167941,Human_RBP_ID_26379653 31213 RMVar_ID_31213 Human_SNP_ID_9320506 A-to-I Human chr1 - 35602159 35602159 35602159 GCCCAGCTAGTTTTTGTGTTTTTCATAGAGACAGGGTCTCACCATGTCATTCAGGTTGGTCTTGA GCCCAGCTAGTTTTTGTGTTTTTCATAGAGACGGGGTCTCACCATGTCATTCAGGTTGGTCTTGA T C PSMB2 Ensembl:ENSG00000126067 Protein coding 3'UTR GSE100210;GSE112787 HepG2 cell line;293 Flip-In T-REx cells,empty vector - 29129909,29967493 RNA-Seq:(High) rs1132067 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_353704,Human_RBP_ID_8167941,Human_RBP_ID_26379653 31214 RMVar_ID_31214 Human_SNP_ID_9320512 A-to-I Human chr1 - 35602183 35602183 35602183 GGATTACAGGCGCACACCACCAATGCCCAGCTAGTTTTTGTGTTTTTCATAGAGACAGGGTCTCA GGATTACAGGCGCACACCACCAATGCCCAGCTGGTTTTTGTGTTTTTCATAGAGACAGGGTCTCA T C PSMB2 Ensembl:ENSG00000126067 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1132065 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8167941,Human_RBP_ID_26379655 31215 RMVar_ID_31215 Human_SNP_ID_9320520 A-to-I Human chr1 - 35602237 35602237 35602237 ACCTCCGCCTCCCGGGCCCAAGTGATCCTCCCATCTCAGCCTCCTGAGTAGCTAGGATTACAGGC ACCTCCGCCTCCCGGGCCCAAGTGATCCTCCCGTCTCAGCCTCCTGAGTAGCTAGGATTACAGGC T C PSMB2 Ensembl:ENSG00000126067 Protein coding 3'UTR GSE38233;GSE100210;GSE112787 cultured B-cells;HepG2 cell line;293 Flip-In T-REx cells,empty vector - 24183664,29129909,29967493 RNA-Seq:(High) rs11550445 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_353705,Human_RBP_ID_26379656 31216 RMVar_ID_31216 Human_SNP_ID_9320531 A-to-I Human chr1 - 35602269 35602269 35602269 GGAGTGCTGTGGCGTAATCTTGGCTCACTGCAACCTCCGCCTCCCGGGCCCAAGTGATCCTCCCA GGAGTGCTGTGGCGTAATCTTGGCTCACTGCACCCTCCGCCTCCCGGGCCCAAGTGATCCTCCCA T G PSMB2 Ensembl:ENSG00000126067 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1172387890 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4047892 31217 RMVar_ID_31217 Human_SNP_ID_9320534 A-to-I Human chr1 - 35602286 35602286 35602286 TCACTCTAGCCCAGGCTGGAGTGCTGTGGCGTAATCTTGGCTCACTGCAACCTCCGCCTCCCGGG TCACTCTAGCCCAGGCTGGAGTGCTGTGGCGTTATCTTGGCTCACTGCAACCTCCGCCTCCCGGG T A PSMB2 Ensembl:ENSG00000126067 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs563648177 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26379661 31218 RMVar_ID_31218 Human_SNP_ID_9320591 A-to-I Human chr1 - 35602550 35602550 35602550 GAGGTTGCAGTGAGCCTAGATCGCGCCACTGTACTCCAGCCTGGCAACAGAGTGAGACTCCGTCT GAGGTTGCAGTGAGCCTAGATCGCGCCACTGTGCTCCAGCCTGGCAACAGAGTGAGACTCCGTCT T C PSMB2 Ensembl:ENSG00000126067 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1021045029 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_353713,Human_RBP_ID_8167945,Human_RBP_ID_8969522,Human_RBP_ID_23303978,Human_RBP_ID_26379674 31219 RMVar_ID_31219 Human_SNP_ID_9320620 A-to-I Human chr1 - 35602636 35602636 35602636 AAAATTAGCTGGGCGTGGTGGCACGCACCCCTAGTCCCAGCTACTGGGGAGGCTGAGACAGGAGA AAAATTAGCTGGGCGTGGTGGCACGCACCCCTGGTCCCAGCTACTGGGGAGGCTGAGACAGGAGA T C PSMB2 Ensembl:ENSG00000126067 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1163494334 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22369411,Human_RBP_ID_23149265,Human_RBP_ID_26379676 31220 RMVar_ID_31220 Human_SNP_ID_9320636 A-to-I Human chr1 - 35602677 35602677 35602677 CCTGACCAACATGGTAAAACCCCGTCTCTACTAAAAATACAAAAATTAGCTGGGCGTGGTGGCAC CCTGACCAACATGGTAAAACCCCGTCTCTACTGAAAATACAAAAATTAGCTGGGCGTGGTGGCAC T C PSMB2 Ensembl:ENSG00000126067 Protein coding 3'UTR GSE100210;GSE99789 HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 29129909,29796672 RNA-Seq:(High) rs1462944591 Functional Loss SNV dbSNP153 33..33 33 - - - 31221 RMVar_ID_31221 Human_SNP_ID_9320643 A-to-I Human chr1 - 35602694 35602694 35602694 CAAGAGAGCGAGACCATCCTGACCAACATGGTAAAACCCCGTCTCTACTAAAAATACAAAAATTA CAAGAGAGCGAGACCATCCTGACCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTA T C PSMB2 Ensembl:ENSG00000126067 Protein coding 3'UTR GSE38233;GSE112787;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;293 Flip-In T-REx cells,empty vector;ASD brains,Fragile X samples from NIH NeuroBioBank;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29967493,30559470,31158229,31158229,31158229 RNA-Seq:(High) rs1316041635 Functional Loss SNV dbSNP153 33..33 33 - - - 31222 RMVar_ID_31222 Human_SNP_ID_9324913 A-to-I Human chr1 - 35621833 35621833 35621833 TGCCACCATACCTAGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACTGTGTTGGCCAGGC TGCCACCATACCTAGCTAATTTTTGTATTTTTGGTAGAGATGGGGTTTCACTGTGTTGGCCAGGC T C PSMB2 Ensembl:ENSG00000126067 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1557453160 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38525,RMVar_hsa_circ_291437,RMVar_hsa_circ_314305,RMVar_hsa_circ_131539,RMVar_hsa_circ_302813,RMVar_hsa_circ_131540 31223 RMVar_ID_31223 Human_SNP_ID_9349251 A-to-I Human chr1 - 35720574 35720574 35720574 CGTGATGCATGCACCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACCCG CGTGATGCATGCACCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCG T C CLSPN Ensembl:ENSG00000092853 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs942441915 Functional Loss SNV dbSNP153 33..33 33 - - - 31224 RMVar_ID_31224 Human_SNP_ID_9352408 A-to-I Human chr1 - 35734615 35734615 35734615 GGAATACAATGGCATGATCTCGGCTTACTGCAACCTCCGCCTCCTAGGTTCAAGCAATTCTGCCT GGAATACAATGGCATGATCTCGGCTTACTGCAGCCTCCGCCTCCTAGGTTCAAGCAATTCTGCCT T C CLSPN Ensembl:ENSG00000092853 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1485035154 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_353772 RMVar_hsa_circ_106242,RMVar_hsa_circ_131544 31225 RMVar_ID_31225 Human_SNP_ID_9352414 A-to-I Human chr1 - 35734639 35734639 35734639 TAGGCTGGCTCTGTCACCTAGGCTGGAATACAATGGCATGATCTCGGCTTACTGCAACCTCCGCC TAGGCTGGCTCTGTCACCTAGGCTGGAATACAGTGGCATGATCTCGGCTTACTGCAACCTCCGCC T C CLSPN Ensembl:ENSG00000092853 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1426578587 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5817336,Human_RBP_ID_10962045,Human_RBP_ID_19449781,Human_RBP_ID_24397349,Human_RBP_ID_24455631,Human_RBP_ID_26379715,Human_RBP_ID_26863669 RMVar_hsa_circ_106242,RMVar_hsa_circ_131544 31226 RMVar_ID_31226 Human_SNP_ID_9352769 A-to-I Human chr1 - 35736158 35736158 35736158 CTTGGAGTGCAGTGGCGTGATCTCGGCTCACCACAATCTCTGCCTCCCAGGTTCAAGCGATTCTC CTTGGAGTGCAGTGGCGTGATCTCGGCTCACCGCAATCTCTGCCTCCCAGGTTCAAGCGATTCTC T C CLSPN Ensembl:ENSG00000092853 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1040749603 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2473917,Human_miRNA_ID_2722971,Human_miRNA_ID_2959703 RMVar_hsa_circ_106242,RMVar_hsa_circ_131544 31227 RMVar_ID_31227 Human_SNP_ID_9374728 A-to-I Human chr1 + 35827869 35827869 35827869 CACCTTCTGGGCTCAAGTGAACCTCCCACCTCAGACTTCCAAGTAGTGGGATTACAGGCATGCAC CACCTTCTGGGCTCAAGTGAACCTCCCACCTCGGACTTCCAAGTAGTGGGATTACAGGCATGCAC A G AGO4 Ensembl:ENSG00000134698 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1336390996 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80625,RMVar_hsa_circ_277392,RMVar_hsa_circ_104871,RMVar_hsa_circ_302618,RMVar_hsa_circ_131557,RMVar_hsa_circ_374681,RMVar_hsa_circ_375521,RMVar_hsa_circ_281686,RMVar_hsa_circ_20973,RMVar_hsa_circ_273295,RMVar_hsa_circ_51389,RMVar_hsa_circ_131563,RMVar_hsa_circ_131565,RMVar_hsa_circ_131566,RMVar_hsa_circ_131567,RMVar_hsa_circ_131564,RMVar_hsa_circ_131562,RMVar_hsa_circ_66372,RMVar_hsa_circ_359854,RMVar_hsa_circ_71874,RMVar_hsa_circ_286569,RMVar_hsa_circ_61025,RMVar_hsa_circ_48318,RMVar_hsa_circ_131569,RMVar_hsa_circ_85700,RMVar_hsa_circ_83707,RMVar_hsa_circ_67283,RMVar_hsa_circ_131574,RMVar_hsa_circ_131576,RMVar_hsa_circ_77611,RMVar_hsa_circ_131575,RMVar_hsa_circ_131573 31228 RMVar_ID_31228 Human_SNP_ID_9374752 A-to-I Human chr1 + 35827945 35827945 35827945 CCTAATTTTTTTTGTAGAGGTGGGGTTTTGCTATGTTGCCCAGTCTGGTCTTGAATTCCTGGGCT CCTAATTTTTTTTGTAGAGGTGGGGTTTTGCTGTGTTGCCCAGTCTGGTCTTGAATTCCTGGGCT A G AGO4 Ensembl:ENSG00000134698 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1172327180 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80625,RMVar_hsa_circ_277392,RMVar_hsa_circ_104871,RMVar_hsa_circ_302618,RMVar_hsa_circ_131557,RMVar_hsa_circ_374681,RMVar_hsa_circ_375521,RMVar_hsa_circ_281686,RMVar_hsa_circ_20973,RMVar_hsa_circ_273295,RMVar_hsa_circ_51389,RMVar_hsa_circ_131563,RMVar_hsa_circ_131565,RMVar_hsa_circ_131566,RMVar_hsa_circ_131567,RMVar_hsa_circ_131564,RMVar_hsa_circ_131562,RMVar_hsa_circ_66372,RMVar_hsa_circ_359854,RMVar_hsa_circ_71874,RMVar_hsa_circ_286569,RMVar_hsa_circ_61025,RMVar_hsa_circ_48318,RMVar_hsa_circ_131569,RMVar_hsa_circ_85700,RMVar_hsa_circ_83707,RMVar_hsa_circ_67283,RMVar_hsa_circ_131574,RMVar_hsa_circ_131576,RMVar_hsa_circ_77611,RMVar_hsa_circ_131575,RMVar_hsa_circ_131573 31229 RMVar_ID_31229 Human_SNP_ID_9374830 A-to-I Human chr1 + 35828258 35828258 35828258 CCCACTGCAGCCTCAGCTTCCTGGGCTCAAGCAATCCTCCCACCTCAGCCTCCTGAGTATCTGGG CCCACTGCAGCCTCAGCTTCCTGGGCTCAAGCGATCCTCCCACCTCAGCCTCCTGAGTATCTGGG A G AGO4 Ensembl:ENSG00000134698 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1329509965 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80625,RMVar_hsa_circ_277392,RMVar_hsa_circ_104871,RMVar_hsa_circ_302618,RMVar_hsa_circ_131557,RMVar_hsa_circ_374681,RMVar_hsa_circ_375521,RMVar_hsa_circ_281686,RMVar_hsa_circ_20973,RMVar_hsa_circ_273295,RMVar_hsa_circ_51389,RMVar_hsa_circ_131563,RMVar_hsa_circ_131565,RMVar_hsa_circ_131566,RMVar_hsa_circ_131567,RMVar_hsa_circ_131564,RMVar_hsa_circ_131562,RMVar_hsa_circ_66372,RMVar_hsa_circ_359854,RMVar_hsa_circ_71874,RMVar_hsa_circ_286569,RMVar_hsa_circ_61025,RMVar_hsa_circ_48318,RMVar_hsa_circ_131569,RMVar_hsa_circ_85700,RMVar_hsa_circ_83707,RMVar_hsa_circ_67283,RMVar_hsa_circ_131574,RMVar_hsa_circ_131576,RMVar_hsa_circ_77611,RMVar_hsa_circ_131575,RMVar_hsa_circ_131573 31230 RMVar_ID_31230 Human_SNP_ID_9374834 A-to-I Human chr1 + 35828272 35828272 35828272 AGCTTCCTGGGCTCAAGCAATCCTCCCACCTCAGCCTCCTGAGTATCTGGGACTACAGGCATGTG AGCTTCCTGGGCTCAAGCAATCCTCCCACCTCTGCCTCCTGAGTATCTGGGACTACAGGCATGTG A T AGO4 Ensembl:ENSG00000134698 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1224355773 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80625,RMVar_hsa_circ_277392,RMVar_hsa_circ_104871,RMVar_hsa_circ_302618,RMVar_hsa_circ_131557,RMVar_hsa_circ_374681,RMVar_hsa_circ_375521,RMVar_hsa_circ_281686,RMVar_hsa_circ_20973,RMVar_hsa_circ_273295,RMVar_hsa_circ_51389,RMVar_hsa_circ_131563,RMVar_hsa_circ_131565,RMVar_hsa_circ_131566,RMVar_hsa_circ_131567,RMVar_hsa_circ_131564,RMVar_hsa_circ_131562,RMVar_hsa_circ_66372,RMVar_hsa_circ_359854,RMVar_hsa_circ_71874,RMVar_hsa_circ_286569,RMVar_hsa_circ_61025,RMVar_hsa_circ_48318,RMVar_hsa_circ_131569,RMVar_hsa_circ_85700,RMVar_hsa_circ_83707,RMVar_hsa_circ_67283,RMVar_hsa_circ_131574,RMVar_hsa_circ_131576,RMVar_hsa_circ_77611,RMVar_hsa_circ_131575,RMVar_hsa_circ_131573 31231 RMVar_ID_31231 Human_SNP_ID_9374913 A-to-I Human chr1 + 35828606 35828606 35828606 CAATGTCGTGATCTCTGCTCACTGCAACCTCCACCTCCCCGGTTCAAGCGATTCTCCTGCCTCAA CAATGTCGTGATCTCTGCTCACTGCAACCTCCGCCTCCCCGGTTCAAGCGATTCTCCTGCCTCAA A G AGO4 Ensembl:ENSG00000134698 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1359954844 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80625,RMVar_hsa_circ_277392,RMVar_hsa_circ_104871,RMVar_hsa_circ_302618,RMVar_hsa_circ_131557,RMVar_hsa_circ_374681,RMVar_hsa_circ_375521,RMVar_hsa_circ_281686,RMVar_hsa_circ_20973,RMVar_hsa_circ_273295,RMVar_hsa_circ_51389,RMVar_hsa_circ_131563,RMVar_hsa_circ_131565,RMVar_hsa_circ_131566,RMVar_hsa_circ_131567,RMVar_hsa_circ_131564,RMVar_hsa_circ_131562,RMVar_hsa_circ_66372,RMVar_hsa_circ_359854,RMVar_hsa_circ_71874,RMVar_hsa_circ_286569,RMVar_hsa_circ_61025,RMVar_hsa_circ_48318,RMVar_hsa_circ_131569,RMVar_hsa_circ_85700,RMVar_hsa_circ_83707,RMVar_hsa_circ_67283,RMVar_hsa_circ_131574,RMVar_hsa_circ_131576,RMVar_hsa_circ_77611,RMVar_hsa_circ_131575,RMVar_hsa_circ_131573 31232 RMVar_ID_31232 Human_SNP_ID_9396303 A-to-I Human chr1 - 35918987 35918987 35918987 GCAGAGAAGATGGCTGATAATAGGGGAACAGGATCACTGTTAAGAATATGGCTGGGTAGATAATT GCAGAGAAGATGGCTGATAATAGGGGAACAGGGTCACTGTTAAGAATATGGCTGGGTAGATAATT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1002304595 Functional Loss SNV dbSNP153 33..33 33 - - - 31233 RMVar_ID_31233 Human_SNP_ID_9414845 A-to-I Human chr1 + 35996081 35996081 35996081 GACAAGGCAGCCAGGCGCACTGGCTCACACCTATAATCCCAACACTTTGGGAGGCCTAGGCAAGA GACAAGGCAGCCAGGCGCACTGGCTCACACCTGTAATCCCAACACTTTGGGAGGCCTAGGCAAGA A G AGO3 Ensembl:ENSG00000126070 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs761917995 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_131627,RMVar_hsa_circ_23771,RMVar_hsa_circ_113604,RMVar_hsa_circ_131617,RMVar_hsa_circ_297112,RMVar_hsa_circ_322874,RMVar_hsa_circ_24806,RMVar_hsa_circ_332159,RMVar_hsa_circ_355623,RMVar_hsa_circ_323700,RMVar_hsa_circ_319233,RMVar_hsa_circ_311024,RMVar_hsa_circ_45586,RMVar_hsa_circ_84669,RMVar_hsa_circ_131622,RMVar_hsa_circ_13008,RMVar_hsa_circ_131623,RMVar_hsa_circ_131620,RMVar_hsa_circ_131621,RMVar_hsa_circ_333331,RMVar_hsa_circ_120386,RMVar_hsa_circ_7068,RMVar_hsa_circ_131628 31234 RMVar_ID_31234 Human_SNP_ID_9415348 A-to-I Human chr1 + 35997880 35997880 35997880 CACCACGCCCAGCTAATTTTTGTGTTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGG CACCACGCCCAGCTAATTTTTGTGTTTTTAGTGGAGACAGGGTTTCACCATGTTGGCCAGGCTGG A G AGO3 Ensembl:ENSG00000126070 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs770006430 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_131627,RMVar_hsa_circ_23771,RMVar_hsa_circ_113604,RMVar_hsa_circ_131617,RMVar_hsa_circ_297112,RMVar_hsa_circ_322874,RMVar_hsa_circ_24806,RMVar_hsa_circ_332159,RMVar_hsa_circ_355623,RMVar_hsa_circ_323700,RMVar_hsa_circ_319233,RMVar_hsa_circ_311024,RMVar_hsa_circ_45586,RMVar_hsa_circ_84669,RMVar_hsa_circ_131622,RMVar_hsa_circ_13008,RMVar_hsa_circ_131623,RMVar_hsa_circ_131620,RMVar_hsa_circ_131621,RMVar_hsa_circ_333331,RMVar_hsa_circ_120386,RMVar_hsa_circ_7068,RMVar_hsa_circ_131628 31235 RMVar_ID_31235 Human_SNP_ID_9415350 A-to-I Human chr1 + 35997886 35997886 35997886 GCCCAGCTAATTTTTGTGTTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTCGA GCCCAGCTAATTTTTGTGTTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGGTCTCGA A G AGO3 Ensembl:ENSG00000126070 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs946466602 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_131627,RMVar_hsa_circ_23771,RMVar_hsa_circ_113604,RMVar_hsa_circ_131617,RMVar_hsa_circ_297112,RMVar_hsa_circ_322874,RMVar_hsa_circ_24806,RMVar_hsa_circ_332159,RMVar_hsa_circ_355623,RMVar_hsa_circ_323700,RMVar_hsa_circ_319233,RMVar_hsa_circ_311024,RMVar_hsa_circ_45586,RMVar_hsa_circ_84669,RMVar_hsa_circ_131622,RMVar_hsa_circ_13008,RMVar_hsa_circ_131623,RMVar_hsa_circ_131620,RMVar_hsa_circ_131621,RMVar_hsa_circ_333331,RMVar_hsa_circ_120386,RMVar_hsa_circ_7068,RMVar_hsa_circ_131628 31236 RMVar_ID_31236 Human_SNP_ID_9416360 A-to-I Human chr1 + 36002506 36002506 36002506 CACATGCCACCACGCCTGGCTAATTTTTTTGTATTTTCAGTAGAGATGGGGTTTCACCATGTTGC CACATGCCACCACGCCTGGCTAATTTTTTTGTGTTTTCAGTAGAGATGGGGTTTCACCATGTTGC A G AGO3 Ensembl:ENSG00000126070 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1394316387 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_131627,RMVar_hsa_circ_23771,RMVar_hsa_circ_113604,RMVar_hsa_circ_131617,RMVar_hsa_circ_297112,RMVar_hsa_circ_322874,RMVar_hsa_circ_24806,RMVar_hsa_circ_332159,RMVar_hsa_circ_355623,RMVar_hsa_circ_323700,RMVar_hsa_circ_319233,RMVar_hsa_circ_311024,RMVar_hsa_circ_45586,RMVar_hsa_circ_84669,RMVar_hsa_circ_131622,RMVar_hsa_circ_13008,RMVar_hsa_circ_131623,RMVar_hsa_circ_131620,RMVar_hsa_circ_131621,RMVar_hsa_circ_333331,RMVar_hsa_circ_120386,RMVar_hsa_circ_7068,RMVar_hsa_circ_131628 31237 RMVar_ID_31237 Human_SNP_ID_9416361 A-to-I Human chr1 + 36002512 36002512 36002512 CCACCACGCCTGGCTAATTTTTTTGTATTTTCAGTAGAGATGGGGTTTCACCATGTTGCCCAGGC CCACCACGCCTGGCTAATTTTTTTGTATTTTCGGTAGAGATGGGGTTTCACCATGTTGCCCAGGC A G AGO3 Ensembl:ENSG00000126070 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1439185958 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_131627,RMVar_hsa_circ_23771,RMVar_hsa_circ_113604,RMVar_hsa_circ_131617,RMVar_hsa_circ_297112,RMVar_hsa_circ_322874,RMVar_hsa_circ_24806,RMVar_hsa_circ_332159,RMVar_hsa_circ_355623,RMVar_hsa_circ_323700,RMVar_hsa_circ_319233,RMVar_hsa_circ_311024,RMVar_hsa_circ_45586,RMVar_hsa_circ_84669,RMVar_hsa_circ_131622,RMVar_hsa_circ_13008,RMVar_hsa_circ_131623,RMVar_hsa_circ_131620,RMVar_hsa_circ_131621,RMVar_hsa_circ_333331,RMVar_hsa_circ_120386,RMVar_hsa_circ_7068,RMVar_hsa_circ_131628 31238 RMVar_ID_31238 Human_SNP_ID_9416365 A-to-I Human chr1 + 36002529 36002529 36002529 TTTTTTTGTATTTTCAGTAGAGATGGGGTTTCACCATGTTGCCCAGGCTGGTTTTGAACTCCTGA TTTTTTTGTATTTTCAGTAGAGATGGGGTTTCCCCATGTTGCCCAGGCTGGTTTTGAACTCCTGA A C AGO3 Ensembl:ENSG00000126070 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1001426731 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_131627,RMVar_hsa_circ_23771,RMVar_hsa_circ_113604,RMVar_hsa_circ_131617,RMVar_hsa_circ_297112,RMVar_hsa_circ_322874,RMVar_hsa_circ_24806,RMVar_hsa_circ_332159,RMVar_hsa_circ_355623,RMVar_hsa_circ_323700,RMVar_hsa_circ_319233,RMVar_hsa_circ_311024,RMVar_hsa_circ_45586,RMVar_hsa_circ_84669,RMVar_hsa_circ_131622,RMVar_hsa_circ_13008,RMVar_hsa_circ_131623,RMVar_hsa_circ_131620,RMVar_hsa_circ_131621,RMVar_hsa_circ_333331,RMVar_hsa_circ_120386,RMVar_hsa_circ_7068,RMVar_hsa_circ_131628 31239 RMVar_ID_31239 Human_SNP_ID_9418325 A-to-I Human chr1 + 36010742 36010742 36010742 CCAGCCTACCAACATAGAGAAACTCCGTGTCTACTAAAAATACAAAATTAGCCAGGCATAGTGGC CCAGCCTACCAACATAGAGAAACTCCGTGTCTGCTAAAAATACAAAATTAGCCAGGCATAGTGGC A G AGO3 Ensembl:ENSG00000126070 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1428108042 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23771,RMVar_hsa_circ_297112,RMVar_hsa_circ_322874,RMVar_hsa_circ_24806,RMVar_hsa_circ_355623,RMVar_hsa_circ_323700,RMVar_hsa_circ_319233,RMVar_hsa_circ_45586,RMVar_hsa_circ_84669,RMVar_hsa_circ_131622,RMVar_hsa_circ_13008,RMVar_hsa_circ_131620,RMVar_hsa_circ_131621,RMVar_hsa_circ_131628,RMVar_hsa_circ_131641,RMVar_hsa_circ_131630,RMVar_hsa_circ_131634,RMVar_hsa_circ_282956,RMVar_hsa_circ_359402,RMVar_hsa_circ_365191,RMVar_hsa_circ_330687,RMVar_hsa_circ_296507,RMVar_hsa_circ_277107,RMVar_hsa_circ_59383,RMVar_hsa_circ_131632,RMVar_hsa_circ_131633,RMVar_hsa_circ_131631,RMVar_hsa_circ_37549,RMVar_hsa_circ_344600,RMVar_hsa_circ_361336,RMVar_hsa_circ_349205,RMVar_hsa_circ_365458,RMVar_hsa_circ_131635,RMVar_hsa_circ_369805,RMVar_hsa_circ_374612,RMVar_hsa_circ_341689,RMVar_hsa_circ_356570,RMVar_hsa_circ_24352,RMVar_hsa_circ_270326,RMVar_hsa_circ_363253,RMVar_hsa_circ_131638,RMVar_hsa_circ_131639,RMVar_hsa_circ_131637,RMVar_hsa_circ_371580,RMVar_hsa_circ_343718,RMVar_hsa_circ_349921,RMVar_hsa_circ_315083,RMVar_hsa_circ_131643,RMVar_hsa_circ_131644,RMVar_hsa_circ_131642,RMVar_hsa_circ_131640 31240 RMVar_ID_31240 Human_SNP_ID_9420047 A-to-I Human chr1 + 36018081 36018081 36018081 CGGCTCACTGCAGCCTCTGCCTCCCGGGATCAAACAATTGTCCTGCCTCAGCCTCCCAAGTAGAA CGGCTCACTGCAGCCTCTGCCTCCCGGGATCACACAATTGTCCTGCCTCAGCCTCCCAAGTAGAA A C AGO3 Ensembl:ENSG00000126070 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1462121658 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23771,RMVar_hsa_circ_297112,RMVar_hsa_circ_322874,RMVar_hsa_circ_355623,RMVar_hsa_circ_323700,RMVar_hsa_circ_319233,RMVar_hsa_circ_45586,RMVar_hsa_circ_84669,RMVar_hsa_circ_131622,RMVar_hsa_circ_131620,RMVar_hsa_circ_131621,RMVar_hsa_circ_131628,RMVar_hsa_circ_131641,RMVar_hsa_circ_131634,RMVar_hsa_circ_282956,RMVar_hsa_circ_359402,RMVar_hsa_circ_365191,RMVar_hsa_circ_330687,RMVar_hsa_circ_277107,RMVar_hsa_circ_59383,RMVar_hsa_circ_131632,RMVar_hsa_circ_131633,RMVar_hsa_circ_131631,RMVar_hsa_circ_37549,RMVar_hsa_circ_361336,RMVar_hsa_circ_349205,RMVar_hsa_circ_365458,RMVar_hsa_circ_131635,RMVar_hsa_circ_369805,RMVar_hsa_circ_374612,RMVar_hsa_circ_341689,RMVar_hsa_circ_356570,RMVar_hsa_circ_24352,RMVar_hsa_circ_270326,RMVar_hsa_circ_363253,RMVar_hsa_circ_131638,RMVar_hsa_circ_131639,RMVar_hsa_circ_131637,RMVar_hsa_circ_371580,RMVar_hsa_circ_349921,RMVar_hsa_circ_315083,RMVar_hsa_circ_131643,RMVar_hsa_circ_131644,RMVar_hsa_circ_131642,RMVar_hsa_circ_123067,RMVar_hsa_circ_351497,RMVar_hsa_circ_131645,RMVar_hsa_circ_65908 31241 RMVar_ID_31241 Human_SNP_ID_9425853 A-to-I Human chr1 + 36042164 36042164 36042164 TGGAGTGCAGTGGCATGACTTTGGCTCACTGCAGCCCCCACCTCCTGGGTTCAAGTGATTGTCAG TGGAGTGCAGTGGCATGACTTTGGCTCACTGCGGCCCCCACCTCCTGGGTTCAAGTGATTGTCAG A G AGO3 Ensembl:ENSG00000126070 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs916137888 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23771,RMVar_hsa_circ_297112,RMVar_hsa_circ_131634,RMVar_hsa_circ_359402,RMVar_hsa_circ_277107,RMVar_hsa_circ_37549,RMVar_hsa_circ_369805,RMVar_hsa_circ_341689,RMVar_hsa_circ_363253,RMVar_hsa_circ_131639,RMVar_hsa_circ_371580,RMVar_hsa_circ_131643,RMVar_hsa_circ_131644,RMVar_hsa_circ_104216,RMVar_hsa_circ_123067,RMVar_hsa_circ_131645,RMVar_hsa_circ_319246,RMVar_hsa_circ_131648,RMVar_hsa_circ_272132,RMVar_hsa_circ_119509,RMVar_hsa_circ_102780,RMVar_hsa_circ_131649,RMVar_hsa_circ_273076,RMVar_hsa_circ_131651,RMVar_hsa_circ_131650,RMVar_hsa_circ_283470,RMVar_hsa_circ_131654,RMVar_hsa_circ_131655,RMVar_hsa_circ_7665,RMVar_hsa_circ_375264,RMVar_hsa_circ_131656 31242 RMVar_ID_31242 Human_SNP_ID_9427378 A-to-I Human chr1 + 36048721 36048717 36048721 AGATGTAGACTGGCTAAATGAATTTTTTTCTCACTCTGGTTTCCAGGCTGGAGTACAGTGGTGCA AGATGTAGACTGGCTAAATGAATTTTTTT____CTCTGGTTTCCAGGCTGGAGTACAGTGGTGCA TCTCA T AGO3 Ensembl:ENSG00000126070 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1557713285 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_3311773 RMVar_hsa_circ_297112,RMVar_hsa_circ_359402,RMVar_hsa_circ_341689,RMVar_hsa_circ_371580,RMVar_hsa_circ_131644,RMVar_hsa_circ_104216,RMVar_hsa_circ_123067,RMVar_hsa_circ_131645,RMVar_hsa_circ_131648,RMVar_hsa_circ_119509,RMVar_hsa_circ_102780,RMVar_hsa_circ_131650,RMVar_hsa_circ_91731,RMVar_hsa_circ_131655,RMVar_hsa_circ_375264,RMVar_hsa_circ_131656,RMVar_hsa_circ_131657 31243 RMVar_ID_31243 Human_SNP_ID_9430705 A-to-I Human chr1 + 36063861 36063861 36063861 ACTTCAAACTCCTGGGCTCAGGCTATCCTCCCACCTCAGCCTCTGAAGTAGCTGGGACTACTCAC ACTTCAAACTCCTGGGCTCAGGCTATCCTCCCCCCTCAGCCTCTGAAGTAGCTGGGACTACTCAC A C AGO3 Ensembl:ENSG00000126070 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982937231 Functional Loss SNV dbSNP153 33..33 33 - - - 31244 RMVar_ID_31244 Human_SNP_ID_9430735 A-to-I Human chr1 + 36064022 36064022 36064022 CCCACATCAGCCTCCCAAAGTGCTGGGATTACAGCCATGAGCCACTGCATCTGGCCAAGATCAAG CCCACATCAGCCTCCCAAAGTGCTGGGATTACGGCCATGAGCCACTGCATCTGGCCAAGATCAAG A G AGO3 Ensembl:ENSG00000126070 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs759003318 Functional Loss SNV dbSNP153 33..33 33 - - - 31245 RMVar_ID_31245 Human_SNP_ID_9431025 A-to-I Human chr1 + 36065056 36065056 36065056 GGGCTTGGCGGTACGTGCCTGTAATCCCAGCTACTGGGAAGGCCGAGGCAGGAGAATGGCTTGAA GGGCTTGGCGGTACGTGCCTGTAATCCCAGCTGCTGGGAAGGCCGAGGCAGGAGAATGGCTTGAA A G AGO3 Ensembl:ENSG00000126070 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1346102019 Functional Loss SNV dbSNP153 33..33 33 - - - 31246 RMVar_ID_31246 Human_SNP_ID_9431944 A-to-I Human chr1 + 36069162 36069162 36069162 GTCTCACTCTGTTGCCCAGGCTGAACTACAGTAGTGTGATCATAGCTCACTACAGCCTCCAACTC GTCTCACTCTGTTGCCCAGGCTGAACTACAGTGGTGTGATCATAGCTCACTACAGCCTCCAACTC A G AGO3 Ensembl:ENSG00000126070 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1397950218 Functional Loss SNV dbSNP153 33..33 33 - - - 31247 RMVar_ID_31247 Human_SNP_ID_9431947 A-to-I Human chr1 + 36069181 36069181 36069181 GCTGAACTACAGTAGTGTGATCATAGCTCACTACAGCCTCCAACTCCTGGGCCCAAACTATCCTC GCTGAACTACAGTAGTGTGATCATAGCTCACTGCAGCCTCCAACTCCTGGGCCCAAACTATCCTC A G AGO3 Ensembl:ENSG00000126070 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs920978028 Functional Loss SNV dbSNP153 33..33 33 - - - 31248 RMVar_ID_31248 Human_SNP_ID_9431953 A-to-I Human chr1 + 36069204 36069204 36069204 TAGCTCACTACAGCCTCCAACTCCTGGGCCCAAACTATCCTCCTGCTTCAGCCTCCCAAGTAGCT TAGCTCACTACAGCCTCCAACTCCTGGGCCCAGACTATCCTCCTGCTTCAGCCTCCCAAGTAGCT A G AGO3 Ensembl:ENSG00000126070 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1319059557 Functional Loss SNV dbSNP153 33..33 33 - - - 31249 RMVar_ID_31249 Human_SNP_ID_9431955 A-to-I Human chr1 + 36069208 36069208 36069208 TCACTACAGCCTCCAACTCCTGGGCCCAAACTATCCTCCTGCTTCAGCCTCCCAAGTAGCTGGGA TCACTACAGCCTCCAACTCCTGGGCCCAAACTGTCCTCCTGCTTCAGCCTCCCAAGTAGCTGGGA A G AGO3 Ensembl:ENSG00000126070 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs781622180 Functional Loss SNV dbSNP153 33..33 33 - - - 31250 RMVar_ID_31250 Human_SNP_ID_9431957 A-to-I Human chr1 + 36069251 36069221 36069252 TCAGCCTCCCAAGTAGCTGGGACTAGAGGTACATGCCACCACACCCAGCTAATTATTTTCTTTTA TCA_______________________________GCCACCACACCCAGCTAATTATTTTCTTTTA AGCCTCCCAAGTAGCTGGGACTAGAGGTACAT A AGO3 Ensembl:ENSG00000126070 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs369399300 Functional Loss DEL dbSNP153 4..34 33 - - - 31251 RMVar_ID_31251 Human_SNP_ID_9431965 A-to-I Human chr1 + 36069251 36069251 36069251 TCAGCCTCCCAAGTAGCTGGGACTAGAGGTACATGCCACCACACCCAGCTAATTATTTTCTTTTA TCAGCCTCCCAAGTAGCTGGGACTAGAGGTACGTGCCACCACACCCAGCTAATTATTTTCTTTTA A G AGO3 Ensembl:ENSG00000126070 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223913343 Functional Loss SNV dbSNP153 33..33 33 - - - 31252 RMVar_ID_31252 Human_SNP_ID_9431972 A-to-I Human chr1 + 36069288 36069288 36069288 ACCACACCCAGCTAATTATTTTCTTTTATTGCAGAGATGGGGTCTCACATGTTGCCAAGGCTGAT ACCACACCCAGCTAATTATTTTCTTTTATTGCGGAGATGGGGTCTCACATGTTGCCAAGGCTGAT A G AGO3 Ensembl:ENSG00000126070 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs942800648 Functional Loss SNV dbSNP153 33..33 33 - - - 31253 RMVar_ID_31253 Human_SNP_ID_9432109 A-to-I Human chr1 + 36069958 36069958 36069958 GGGTGCCTGTAATCCCAGCTACTCGGGAGGCTAAGGTGGGAGAATTGCTTGGACCCAGGTGGCAG GGGTGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGTGGGAGAATTGCTTGGACCCAGGTGGCAG A G AGO3 Ensembl:ENSG00000126070 Protein coding 3'UTR GSE100210;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T4 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs1557724150 Functional Loss SNV dbSNP153 33..33 33 - - - 31254 RMVar_ID_31254 Human_SNP_ID_9450395 A-to-I Human chr1 - 36138914 36138914 36138914 CTTCTGCCTCAGCCTCCCGAGTAGCTGCGATTACAGGCATGCACCACCATGCCCGGCTAATTTTA CTTCTGCCTCAGCCTCCCGAGTAGCTGCGATTGCAGGCATGCACCACCATGCCCGGCTAATTTTA T C TRAPPC3 Ensembl:ENSG00000054116 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs76796218 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29890,RMVar_hsa_circ_103553,RMVar_hsa_circ_116160,RMVar_hsa_circ_131663,RMVar_hsa_circ_131662 31255 RMVar_ID_31255 Human_SNP_ID_9450494 A-to-I Human chr1 - 36139235 36139235 36139235 AGAATTGCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCCGAGATCACATCACTGCATTCCATCC AGAATTGCTTGAACCCAGGAGGCGGAGGTTGCGGTGAGCCGAGATCACATCACTGCATTCCATCC T C TRAPPC3 Ensembl:ENSG00000054116 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1190097545 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29890,RMVar_hsa_circ_103553,RMVar_hsa_circ_116160,RMVar_hsa_circ_131663,RMVar_hsa_circ_131662 31256 RMVar_ID_31256 Human_SNP_ID_9450503 A-to-I Human chr1 - 36139251 36139251 36139251 CAGGAGGCTGAGGCAGAGAATTGCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCCGAGATCACA CAGGAGGCTGAGGCAGAGAATTGCTTGAACCCGGGAGGCGGAGGTTGCAGTGAGCCGAGATCACA T C TRAPPC3 Ensembl:ENSG00000054116 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1379396663 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29890,RMVar_hsa_circ_103553,RMVar_hsa_circ_116160,RMVar_hsa_circ_131663,RMVar_hsa_circ_131662 31257 RMVar_ID_31257 Human_SNP_ID_9450520 A-to-I Human chr1 - 36139361 36139361 36139361 ACAAGATCAGGAGTTCAAGACCAGCCTGGCCAAGATGGTGAAACCCCATCTCTACTAAAAATACA ACAAGATCAGGAGTTCAAGACCAGCCTGGCCAGGATGGTGAAACCCCATCTCTACTAAAAATACA T C TRAPPC3 Ensembl:ENSG00000054116 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1444824515 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29890,RMVar_hsa_circ_103553,RMVar_hsa_circ_116160,RMVar_hsa_circ_131663,RMVar_hsa_circ_131662 31258 RMVar_ID_31258 Human_SNP_ID_9451785 A-to-I Human chr1 - 36144382 36144382 36144382 CCTCCGCCTCCCAAAGTGCTGGGATTATAGGCATGAGCCACCATGCCCAGCCAGAAAGTTGTTTA CCTCCGCCTCCCAAAGTGCTGGGATTATAGGCGTGAGCCACCATGCCCAGCCAGAAAGTTGTTTA T C TRAPPC3 Ensembl:ENSG00000054116 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992145346 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116160,RMVar_hsa_circ_131662,RMVar_hsa_circ_131666,RMVar_hsa_circ_106792,RMVar_hsa_circ_126665,RMVar_hsa_circ_131667 31259 RMVar_ID_31259 Human_SNP_ID_9451788 A-to-I Human chr1 - 36144388 36144388 36144388 CCCCTGCCTCCGCCTCCCAAAGTGCTGGGATTATAGGCATGAGCCACCATGCCCAGCCAGAAAGT CCCCTGCCTCCGCCTCCCAAAGTGCTGGGATTGTAGGCATGAGCCACCATGCCCAGCCAGAAAGT T C TRAPPC3 Ensembl:ENSG00000054116 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917876096 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116160,RMVar_hsa_circ_131662,RMVar_hsa_circ_131666,RMVar_hsa_circ_106792,RMVar_hsa_circ_126665,RMVar_hsa_circ_131667 31260 RMVar_ID_31260 Human_SNP_ID_9452589 A-to-I Human chr1 - 36147247 36147247 36147247 CCGATCTCAGCTCACTGCAGCCTCCACCTCCCAGGTTCAAAAGATTCTCCTGCCTCAGCCTCCCG CCGATCTCAGCTCACTGCAGCCTCCACCTCCCGGGTTCAAAAGATTCTCCTGCCTCAGCCTCCCG T C TRAPPC3 Ensembl:ENSG00000054116 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs775674555 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116160,RMVar_hsa_circ_131662,RMVar_hsa_circ_131666,RMVar_hsa_circ_106792,RMVar_hsa_circ_126665,RMVar_hsa_circ_131667 31261 RMVar_ID_31261 Human_SNP_ID_9452668 A-to-I Human chr1 - 36147535 36147535 36147535 AGTTCAAGCAGTCCTCCCGCCTCAGCCTCCCAAGTAGCTGGTACTATAGGTGTGCACCACCATGC AGTTCAAGCAGTCCTCCCGCCTCAGCCTCCCAGGTAGCTGGTACTATAGGTGTGCACCACCATGC T C TRAPPC3 Ensembl:ENSG00000054116 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1369430707 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116160,RMVar_hsa_circ_131662,RMVar_hsa_circ_131666,RMVar_hsa_circ_106792,RMVar_hsa_circ_126665,RMVar_hsa_circ_131667 31262 RMVar_ID_31262 Human_SNP_ID_9476645 A-to-I Human chr1 + 36234068 36234068 36234068 GCCTGGACCTCTTGGGCCCAGGGAGTCCTCCCACCTCAGCCTCCTGAGTAGCTAGGACTATAGGT GCCTGGACCTCTTGGGCCCAGGGAGTCCTCCCCCCTCAGCCTCCTGAGTAGCTAGGACTATAGGT A C THRAP3 Ensembl:ENSG00000054118 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1276930025 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81186,RMVar_hsa_circ_103857,RMVar_hsa_circ_131672,RMVar_hsa_circ_131673 31263 RMVar_ID_31263 Human_SNP_ID_9476663 A-to-I Human chr1 + 36234136 36234136 36234136 CACCACCATGCCTGGCTAATTTTTGTAGTTTTATAGAGACAGGGTTTCACCATGTTGCCCAGGCT CACCACCATGCCTGGCTAATTTTTGTAGTTTTGTAGAGACAGGGTTTCACCATGTTGCCCAGGCT A G THRAP3 Ensembl:ENSG00000054118 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs774430772 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10966229 RMVar_hsa_circ_81186,RMVar_hsa_circ_103857,RMVar_hsa_circ_131672,RMVar_hsa_circ_131673 31264 RMVar_ID_31264 Human_SNP_ID_9477160 A-to-I Human chr1 + 36235993 36235993 36235993 ATGTCGGACTGGGCGTGGTTGCTCCCACCTGTAATCCCAGGACTTTGGGAGGCCGAGGTGGGCAG ATGTCGGACTGGGCGTGGTTGCTCCCACCTGTGATCCCAGGACTTTGGGAGGCCGAGGTGGGCAG A G THRAP3 Ensembl:ENSG00000054118 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs762613395 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81186,RMVar_hsa_circ_103857,RMVar_hsa_circ_131672,RMVar_hsa_circ_131673 31265 RMVar_ID_31265 Human_SNP_ID_9477852 A-to-I Human chr1 + 36238237 36238237 36238237 CCATCTGCCCACCTCAGCTTCCTCAGAGTGCTAGGATTATATGGGTAAAACATCGTGCTCAGCCT CCATCTGCCCACCTCAGCTTCCTCAGAGTGCTGGGATTATATGGGTAAAACATCGTGCTCAGCCT A G THRAP3 Ensembl:ENSG00000054118 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1413250238 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81186,RMVar_hsa_circ_103857,RMVar_hsa_circ_131672,RMVar_hsa_circ_131673 31266 RMVar_ID_31266 Human_SNP_ID_9478232 A-to-I Human chr1 + 36239392 36239392 36239392 GGCTTTCAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGATGGGATTACAGGTTTGCGCCACCATG GGCTTTCAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGATGGGATTACAGGTTTGCGCCACCATG A G THRAP3 Ensembl:ENSG00000054118 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs193147315 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10966379 RMVar_hsa_circ_81186,RMVar_hsa_circ_103857,RMVar_hsa_circ_131672,RMVar_hsa_circ_131673 31267 RMVar_ID_31267 Human_SNP_ID_9480957 A-to-I Human chr1 + 36247973 36247973 36247973 ACGATCTTGGCTCACTGCAACCTCCACCTCCCAGGTTCAAGCGATTTTCCTGCCTCAGCCCCCCG ACGATCTTGGCTCACTGCAACCTCCACCTCCCGGGTTCAAGCGATTTTCCTGCCTCAGCCCCCCG A G THRAP3 Ensembl:ENSG00000054118 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1335247152 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81186,RMVar_hsa_circ_103857,RMVar_hsa_circ_131672,RMVar_hsa_circ_131673 31268 RMVar_ID_31268 Human_SNP_ID_9487260 A-to-I Human chr1 + 36270345 36270345 36270345 CAGCCAGGGAGGTTGAGGCTGCAGTGAGCTATAATCGAGCCACTGCACTCCAGTCTGAAACAACA CAGCCAGGGAGGTTGAGGCTGCAGTGAGCTATGATCGAGCCACTGCACTCCAGTCTGAAACAACA A G THRAP3 Ensembl:ENSG00000054118 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1372038001 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23303980 RMVar_hsa_circ_81186,RMVar_hsa_circ_113465,RMVar_hsa_circ_103857,RMVar_hsa_circ_131672,RMVar_hsa_circ_131673,RMVar_hsa_circ_96633,RMVar_hsa_circ_131674,RMVar_hsa_circ_131675 31269 RMVar_ID_31269 Human_SNP_ID_9487444 A-to-I Human chr1 + 36270739 36270739 36270739 AGCTGGGATTACAGGCATGCCCCACCACGCCTAGCGAATTTTGTATTTTTAGTAGAGATGAGGTT AGCTGGGATTACAGGCATGCCCCACCACGCCTCGCGAATTTTGTATTTTTAGTAGAGATGAGGTT A C THRAP3 Ensembl:ENSG00000054118 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs990483367 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81186,RMVar_hsa_circ_113465,RMVar_hsa_circ_103857,RMVar_hsa_circ_131672,RMVar_hsa_circ_131673,RMVar_hsa_circ_96633,RMVar_hsa_circ_131674,RMVar_hsa_circ_131675 31270 RMVar_ID_31270 Human_SNP_ID_9494852 A-to-I Human chr1 + 36297548 36297548 36297548 TCAGCTCACTGCAACCTCCGCCTCGCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGC TCAGCTCACTGCAACCTCCGCCTCGCGGGTTCCAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGC A C THRAP3 Ensembl:ENSG00000054118 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1056497340 Functional Loss SNV dbSNP153 33..33 33 - - - 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_131685 31271 RMVar_ID_31271 Human_SNP_ID_9494859 A-to-I Human chr1 + 36297566 36297566 36297566 CGCCTCGCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGTGCCCA CGCCTCGCGGGTTCAAGCAATTCTCCTGCCTCCGCCTCCTGAGTAGCTGGGATTACAGGTGCCCA A C THRAP3 Ensembl:ENSG00000054118 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1421853536 Functional Loss SNV dbSNP153 33..33 33 - - - 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_131685 31272 RMVar_ID_31272 Human_SNP_ID_9494864 A-to-I Human chr1 + 36297588 36297588 36297588 CTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGTGCCCACTACCACGCCCAGCTAATTTTT CTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTGCAGGTGCCCACTACCACGCCCAGCTAATTTTT A G THRAP3 Ensembl:ENSG00000054118 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1384166529 Functional Loss SNV dbSNP153 33..33 33 - - - 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_131685 31273 RMVar_ID_31273 Human_SNP_ID_9494949 A-to-I Human chr1 + 36297943 36297943 36297943 CCGAGGCAGGAAGATCACGTGGTCAGGAGTTCAAGACCAGCCTGGCCAATATCGTGAAACCCTGT CCGAGGCAGGAAGATCACGTGGTCAGGAGTTCGAGACCAGCCTGGCCAATATCGTGAAACCCTGT A G THRAP3 Ensembl:ENSG00000054118 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1043636620 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10967995 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_131685 31274 RMVar_ID_31274 Human_SNP_ID_9495402 A-to-I Human chr1 + 36299524 36299524 36299524 CTTTTTTTTTTGTTTTGTTTTGTTTTTGAGGTAGAGTCTCGCTCTGTCACCCAGGCTGGAGTGCA CTTTTTTTTTTGTTTTGTTTTGTTTTTGAGGTCGAGTCTCGCTCTGTCACCCAGGCTGGAGTGCA A C THRAP3 Ensembl:ENSG00000054118 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1208987284 Functional Loss SNV dbSNP153 33..33 33 - - - 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_131685 31275 RMVar_ID_31275 Human_SNP_ID_9499295 A-to-I Human chr1 + 36312973 36312973 36312973 TGACTTTGTGGTCTGCCCGGCTTGGCCTCCCAAAGTGCTGGGATTACAGATGTGAGCCACCACAC TGACTTTGTGGTCTGCCCGGCTTGGCCTCCCAGAGTGCTGGGATTACAGATGTGAGCCACCACAC A G SH3D21 Ensembl:ENSG00000214193 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1383581698 Functional Loss SNV dbSNP153 33..33 33 - - - 31276 RMVar_ID_31276 Human_SNP_ID_9502937 A-to-I Human chr1 + 36324478 36324478 36324478 TGCCCTGTCTCCACGGGGCCCCCCCATCATGGACCTCCCCTCCCTTGCTGGAGCTAGAATGAGGG TGCCCTGTCTCCACGGGGCCCCCCCATCATGGTCCTCCCCTCCCTTGCTGGAGCTAGAATGAGGG A T SH3D21 Ensembl:ENSG00000214193 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs560925255 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3332876,Human_RBP_ID_5234317,Human_RBP_ID_5312470,Human_RBP_ID_21879918,Human_RBP_ID_21962363,Human_RBP_ID_22469732 31277 RMVar_ID_31277 Human_SNP_ID_9503219 A-to-I Human chr1 + 36325686 36325686 36325686 CCTGCCTCAGCTTCCCAAGTAGCTGGGACTACAGGCGCCTGCCACCACGCCTGGCTAATTTTTTG CCTGCCTCAGCTTCCCAAGTAGCTGGGACTACGGGCGCCTGCCACCACGCCTGGCTAATTTTTTG A G SH3D21 Ensembl:ENSG00000214193 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1420009360 Functional Loss SNV dbSNP153 33..33 33 - - - 31278 RMVar_ID_31278 Human_SNP_ID_9503997 A-to-I Human chr1 + 36328665 36328665 36328665 ACGGTAGCACACACCTATAGTTCCTGCTACTCAGGAGGCTAAGGTGGGAGGATCGCTTGAGCCCA ACGGTAGCACACACCTATAGTTCCTGCTACTCGGGAGGCTAAGGTGGGAGGATCGCTTGAGCCCA A G SH3D21 Ensembl:ENSG00000214193 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1001068633 Functional Loss SNV dbSNP153 33..33 33 - - - 31279 RMVar_ID_31279 Human_SNP_ID_9513372 A-to-I Human chr1 - 36363103 36363103 36363103 TTGCCCAGGCTGAAGTGCAGTGGCGTGATCTCAGCTCACTGTAGACTCCGTGTCCTGGGTTCAAG TTGCCCAGGCTGAAGTGCAGTGGCGTGATCTCCGCTCACTGTAGACTCCGTGTCCTGGGTTCAAG T G STK40 Ensembl:ENSG00000196182 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1437092253 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6819,RMVar_hsa_circ_266513,RMVar_hsa_circ_265897,RMVar_hsa_circ_337877,RMVar_hsa_circ_327095 31280 RMVar_ID_31280 Human_SNP_ID_9537221 A-to-I Human chr1 - 36457103 36457101 36457103 CCCAGCTAATTTTTTGTATTTTTAGTAGAGACAGGGTTTCACCGTGTTAGCCAGGATGATCCCAA CCCAGCTAATTTTTTGTATTTTTAGTAGAGAC__GGTTTCACCGTGTTAGCCAGGATGATCCCAA CCT C MRPS15 Ensembl:ENSG00000116898 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1016466310 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_83664,RMVar_hsa_circ_131708 31281 RMVar_ID_31281 Human_SNP_ID_9537223 A-to-I Human chr1 - 36457103 36457103 36457103 CCCAGCTAATTTTTTGTATTTTTAGTAGAGACAGGGTTTCACCGTGTTAGCCAGGATGATCCCAA CCCAGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGATCCCAA T C MRPS15 Ensembl:ENSG00000116898 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1453876245 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83664,RMVar_hsa_circ_131708 31282 RMVar_ID_31282 Human_SNP_ID_9537224 A-to-I Human chr1 - 36457103 36457103 36457103 CCCAGCTAATTTTTTGTATTTTTAGTAGAGACAGGGTTTCACCGTGTTAGCCAGGATGATCCCAA CCCAGCTAATTTTTTGTATTTTTAGTAGAGACCGGGTTTCACCGTGTTAGCCAGGATGATCCCAA T G MRPS15 Ensembl:ENSG00000116898 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1453876245 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83664,RMVar_hsa_circ_131708 31283 RMVar_ID_31283 Human_SNP_ID_9537723 A-to-I Human chr1 - 36459209 36459209 36459209 TTGTGTTTTTGGTAGAGACAGGATTTTGTCATATTGCCCAGGCTGATCTCGAACTCCTGAGCTCA TTGTGTTTTTGGTAGAGACAGGATTTTGTCATTTTGCCCAGGCTGATCTCGAACTCCTGAGCTCA T A MRPS15 Ensembl:ENSG00000116898 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs897096963 Functional Loss SNV dbSNP153 33..33 33 - - - 31284 RMVar_ID_31284 Human_SNP_ID_9537732 A-to-I Human chr1 - 36459246 36459246 36459246 GGGACCAAAGGCATGCACAACCATGTCAAGCTAATTTTTGTGTTTTTGGTAGAGACAGGATTTTG GGGACCAAAGGCATGCACAACCATGTCAAGCTTATTTTTGTGTTTTTGGTAGAGACAGGATTTTG T A MRPS15 Ensembl:ENSG00000116898 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs763708891 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10968993 31285 RMVar_ID_31285 Human_SNP_ID_9537743 A-to-I Human chr1 - 36459299 36459299 36459299 AGCGCAACTTCTGGGGCTCCAGCAATTCTCCTACCTCAGGCTCCCAAGTAGCTGGGACCAAAGGC AGCGCAACTTCTGGGGCTCCAGCAATTCTCCTTCCTCAGGCTCCCAAGTAGCTGGGACCAAAGGC T A MRPS15 Ensembl:ENSG00000116898 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs989420804 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10968997,Human_RBP_ID_22558677 31286 RMVar_ID_31286 Human_SNP_ID_9537751 A-to-I Human chr1 - 36459333 36459333 36459333 GCAGTCAGTGGCAGGTGTGATCATGGCTCACTACAGCGCAACTTCTGGGGCTCCAGCAATTCTCC GCAGTCAGTGGCAGGTGTGATCATGGCTCACTGCAGCGCAACTTCTGGGGCTCCAGCAATTCTCC T C MRPS15 Ensembl:ENSG00000116898 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs922148436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5819546,Human_RBP_ID_10968999 31287 RMVar_ID_31287 Human_SNP_ID_9537756 A-to-I Human chr1 - 36459367 36459367 36459367 AGACCGGATCTCACTCTGTCACTCAGGCTGGAATGCAGTCAGTGGCAGGTGTGATCATGGCTCAC AGACCGGATCTCACTCTGTCACTCAGGCTGGATTGCAGTCAGTGGCAGGTGTGATCATGGCTCAC T A MRPS15 Ensembl:ENSG00000116898 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1183417373 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10969002 31288 RMVar_ID_31288 Human_SNP_ID_9784541 A-to-I Human chr1 - 37462543 37462543 37462543 TTGCTCAGTTGCCCAGGCCGGAGTGCCATGGAACGATCTCGGCTCACTGCAACCTCCGCCTCCCT TTGCTCAGTTGCCCAGGCCGGAGTGCCATGGAGCGATCTCGGCTCACTGCAACCTCCGCCTCCCT T C LINC01137 Ensembl:ENSG00000233621 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1401738059 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8310265 31289 RMVar_ID_31289 Human_SNP_ID_9791865 A-to-I Human chr1 - 37491511 37491511 37491511 ACATTTTTATTTTGTAATGATGGCTTCTTGCTATGTTGCCCAGGCTGGCCTCAAGCAGTCCTCCT ACATTTTTATTTTGTAATGATGGCTTCTTGCTGTGTTGCCCAGGCTGGCCTCAAGCAGTCCTCCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs561981630 Functional Loss SNV dbSNP153 33..33 33 - - - 31290 RMVar_ID_31290 Human_SNP_ID_9793828 A-to-I Human chr1 - 37498606 37498606 37498606 GGGCAACATGGCGAGACTCCCGTCTCTACAAAAAAACACAGTAATTAACTGGACGTGATGGCATG GGGCAACATGGCGAGACTCCCGTCTCTACAAACAAACACAGTAATTAACTGGACGTGATGGCATG T G MEAF6 Ensembl:ENSG00000163875 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1382934664 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24693349 31291 RMVar_ID_31291 Human_SNP_ID_9793849 A-to-I Human chr1 - 37498704 37498704 37498704 TATAGTGGCCAGGTGCTGTGGCTCATACCTGTAATTCCAGCAATTTGGGAGGCTGAGGTGGAGGG TATAGTGGCCAGGTGCTGTGGCTCATACCTGTTATTCCAGCAATTTGGGAGGCTGAGGTGGAGGG T A MEAF6 Ensembl:ENSG00000163875 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1557605540 Functional Loss SNV dbSNP153 33..33 33 - - - 31292 RMVar_ID_31292 Human_SNP_ID_9793893 A-to-I Human chr1 - 37498910 37498910 37498910 CCTAGGCTTGATCCTCCTGCCTCGGCCTCCCAAAGTGCTGGGTTTACAGGCATGAACCACACCAC CCTAGGCTTGATCCTCCTGCCTCGGCCTCCCAGAGTGCTGGGTTTACAGGCATGAACCACACCAC T C MEAF6 Ensembl:ENSG00000163875 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1557605633 Functional Loss SNV dbSNP153 33..33 33 - - - 31293 RMVar_ID_31293 Human_SNP_ID_9793915 A-to-I Human chr1 - 37498994 37498994 37498994 GGCATGTGCCACCATGCCTAGCTAGTTTCTGTATTGTTTTGTAGAGATGGGGTTTTGCCATGCTG GGCATGTGCCACCATGCCTAGCTAGTTTCTGTGTTGTTTTGTAGAGATGGGGTTTTGCCATGCTG T C MEAF6 Ensembl:ENSG00000163875 Protein coding intron GSE38233;GSE100210;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,frontal_cortex - 24183664,29129909,30559470 RNA-Seq:(High) rs764412664 Functional Loss SNV dbSNP153 33..33 33 - - - 31294 RMVar_ID_31294 Human_SNP_ID_9793927 A-to-I Human chr1 - 37499064 37499064 37499064 TCATTGCAGCTTTGACCTCCTGGGCTCAGGCAATCCTCCCACCTCATCCTCCTAAGTAGCTGGGA TCATTGCAGCTTTGACCTCCTGGGCTCAGGCAGTCCTCCCACCTCATCCTCCTAAGTAGCTGGGA T C MEAF6 Ensembl:ENSG00000163875 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1460410230 Functional Loss SNV dbSNP153 33..33 33 - - - 31295 RMVar_ID_31295 Human_SNP_ID_9794140 A-to-I Human chr1 - 37500064 37500064 37500064 GGCCTCAGGTGATCCACCTGCCTCGGCCTCCCAAAGTGCTGGGATTACTGGCATGAGCCACGGTG GGCCTCAGGTGATCCACCTGCCTCGGCCTCCCTAAGTGCTGGGATTACTGGCATGAGCCACGGTG T A MEAF6 Ensembl:ENSG00000163875 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1036132898 Functional Loss SNV dbSNP153 33..33 33 - - - 31296 RMVar_ID_31296 Human_SNP_ID_9794141 A-to-I Human chr1 - 37500064 37500064 37500064 GGCCTCAGGTGATCCACCTGCCTCGGCCTCCCAAAGTGCTGGGATTACTGGCATGAGCCACGGTG GGCCTCAGGTGATCCACCTGCCTCGGCCTCCCGAAGTGCTGGGATTACTGGCATGAGCCACGGTG T C MEAF6 Ensembl:ENSG00000163875 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1036132898 Functional Loss SNV dbSNP153 33..33 33 - - - 31297 RMVar_ID_31297 Human_SNP_ID_9794175 A-to-I Human chr1 - 37500196 37500196 37500196 TGCTTCCTGGGTTCAAACGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCGTGCA TGCTTCCTGGGTTCAAACGATTCTCCTGCCTCCGCCTCCTGAGTAGCTGGGATTACAGGCGTGCA T G MEAF6 Ensembl:ENSG00000163875 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1386426663 Functional Loss SNV dbSNP153 33..33 33 - - - 31298 RMVar_ID_31298 Human_SNP_ID_9794356 A-to-I Human chr1 - 37500943 37500943 37500943 AGACCCTATACATACCTGTTTCCATGCCTCCTAGAAGTTCCGAAGCCAGGGTAAGAGTTCTCATT AGACCCTATACATACCTGTTTCCATGCCTCCTGGAAGTTCCGAAGCCAGGGTAAGAGTTCTCATT T C MIR5581,MEAF6 Ensembl:ENSG00000263675,Ensembl:ENSG00000163875 miRNA,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1455837973 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5158781,Human_RBP_ID_17224550 31299 RMVar_ID_31299 Human_SNP_ID_9796501 A-to-I Human chr1 - 37508981 37508981 37508981 GCAGTCCTCCTGCCTCGGCCTCCCAAGTAGCTAGGACCACAGGCATCTGTCACCACACCTGGCTA GCAGTCCTCCTGCCTCGGCCTCCCAAGTAGCTGGGACCACAGGCATCTGTCACCACACCTGGCTA T C MEAF6 Ensembl:ENSG00000163875 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs888878480 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20638 31300 RMVar_ID_31300 Human_SNP_ID_9807407 A-to-I Human chr1 - 37549497 37549497 37549497 GTAGCTCCTGAGTGGGAGGATTACTTGAGCCTAGGAGGTTGAGGCTGCGGTGAACAGTGATCATA GTAGCTCCTGAGTGGGAGGATTACTTGAGCCTGGGAGGTTGAGGCTGCGGTGAACAGTGATCATA T C SNIP1 Ensembl:ENSG00000163877 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432647000 Functional Loss SNV dbSNP153 33..33 33 - - - 31301 RMVar_ID_31301 Human_SNP_ID_9807741 A-to-I Human chr1 - 37551032 37551032 37551032 GGAGTGCAATGGCGTGATCTTGGCTCACTGCAATCTCCCCTTCCCAGGTTCAAGTGATTCTCCTG GGAGTGCAATGGCGTGATCTTGGCTCACTGCAGTCTCCCCTTCCCAGGTTCAAGTGATTCTCCTG T C SNIP1 Ensembl:ENSG00000163877 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs765484817 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5642278 31302 RMVar_ID_31302 Human_SNP_ID_9816262 A-to-I Human chr1 - 37585157 37585157 37585157 CTACTTGGGAGGCTGAGGCTGGGGAATCGCTTAAACCCGGGAGGCGGAGGTTGCAGTGAGCCAAG CTACTTGGGAGGCTGAGGCTGGGGAATCGCTTGAACCCGGGAGGCGGAGGTTGCAGTGAGCCAAG T C GNL2 Ensembl:ENSG00000134697 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1460103884 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_131732,RMVar_hsa_circ_370785,RMVar_hsa_circ_324515,RMVar_hsa_circ_56579,RMVar_hsa_circ_339516,RMVar_hsa_circ_289555,RMVar_hsa_circ_86186,RMVar_hsa_circ_131736,RMVar_hsa_circ_131737,RMVar_hsa_circ_131738,RMVar_hsa_circ_107846 31303 RMVar_ID_31303 Human_SNP_ID_9816303 A-to-I Human chr1 - 37585332 37585332 37585332 AAATGTGGCCAGACGCAGTGGCTCACACCTGTAATGCTAGCACTTTGGGAGGCTGAGGCGGGCGG AAATGTGGCCAGACGCAGTGGCTCACACCTGTCATGCTAGCACTTTGGGAGGCTGAGGCGGGCGG T G GNL2 Ensembl:ENSG00000134697 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1206247180 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_131732,RMVar_hsa_circ_370785,RMVar_hsa_circ_324515,RMVar_hsa_circ_56579,RMVar_hsa_circ_339516,RMVar_hsa_circ_289555,RMVar_hsa_circ_86186,RMVar_hsa_circ_131736,RMVar_hsa_circ_131737,RMVar_hsa_circ_131738,RMVar_hsa_circ_107846 31304 RMVar_ID_31304 Human_SNP_ID_9840428 A-to-I Human chr1 - 37684456 37684456 37684456 TGCCACCACGCCTGGCTAATTTTTGTACTTTTAGTAGAGAGGCGGTTTCACCATGTTGGCTAGGC TGCCACCACGCCTGGCTAATTTTTGTACTTTTGGTAGAGAGGCGGTTTCACCATGTTGGCTAGGC T C C1orf109 Ensembl:ENSG00000116922 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1057368997 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70976 31305 RMVar_ID_31305 Human_SNP_ID_9840762 A-to-I Human chr1 - 37685544 37685541 37685544 GTCTCTACAAAAAATACAAAAATTAGCCAGGCATGGTGGTATGTGCCTGAAGTCTGTAATCCCAG GTCTCTACAAAAAATACAAAAATTAGCCAGGC___GTGGTATGTGCCTGAAGTCTGTAATCCCAG CCAT C C1orf109 Ensembl:ENSG00000116922 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1209934150 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_70976 31306 RMVar_ID_31306 Human_SNP_ID_9840764 A-to-I Human chr1 - 37685544 37685544 37685544 GTCTCTACAAAAAATACAAAAATTAGCCAGGCATGGTGGTATGTGCCTGAAGTCTGTAATCCCAG GTCTCTACAAAAAATACAAAAATTAGCCAGGCCTGGTGGTATGTGCCTGAAGTCTGTAATCCCAG T G C1orf109 Ensembl:ENSG00000116922 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1275450240 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70976 31307 RMVar_ID_31307 Human_SNP_ID_9840769 A-to-I Human chr1 - 37685561 37685561 37685561 CAACATGGTGAAACGCCGTCTCTACAAAAAATACAAAAATTAGCCAGGCATGGTGGTATGTGCCT CAACATGGTGAAACGCCGTCTCTACAAAAAATGCAAAAATTAGCCAGGCATGGTGGTATGTGCCT T C C1orf109 Ensembl:ENSG00000116922 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs960379196 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70976 31308 RMVar_ID_31308 Human_SNP_ID_9840808 A-to-I Human chr1 - 37685667 37685665 37685667 AAAGAATTTGGGGTCTGGGCGTGGTGGCTCACACCTGTAATCCCAGCCCTTTGGGAAGCTGAGGT AAAGAATTTGGGGTCTGGGCGTGGTGGCTCAC__CTGTAATCCCAGCCCTTTGGGAAGCTGAGGT GGT G C1orf109 Ensembl:ENSG00000116922 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1469417255 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_70976 31309 RMVar_ID_31309 Human_SNP_ID_9841093 A-to-I Human chr1 - 37686833 37686833 37686833 AAACTCCTGACCTCAGGTGATCCACCCCGCTCAGCCTCCCAAAGCTGGGATTACAGGCAACAGCC AAACTCCTGACCTCAGGTGATCCACCCCGCTCTGCCTCCCAAAGCTGGGATTACAGGCAACAGCC T A C1orf109 Ensembl:ENSG00000116922 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1039765781 Functional Loss SNV dbSNP153 33..33 33 - - - 31310 RMVar_ID_31310 Human_SNP_ID_9841121 A-to-I Human chr1 - 37686915 37686915 37686915 GGGTCTACAGGTGTGCACCACCACACCTGGCTAATTTTTGTATATTTAGTAGAGACGGGGTTTTG GGGTCTACAGGTGTGCACCACCACACCTGGCTGATTTTTGTATATTTAGTAGAGACGGGGTTTTG T C C1orf109 Ensembl:ENSG00000116922 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1317947798 Functional Loss SNV dbSNP153 33..33 33 - - - 31311 RMVar_ID_31311 Human_SNP_ID_9841358 A-to-I Human chr1 - 37687532 37687532 37687532 TTGCCCAGGCTGGTCTCAAATTCCTGGCTTCAAGCTGTCCTCTGGCCTTGCCCTCCCAAACTACT TTGCCCAGGCTGGTCTCAAATTCCTGGCTTCAGGCTGTCCTCTGGCCTTGCCCTCCCAAACTACT T C C1orf109 Ensembl:ENSG00000116922 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1166538653 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10971675 31312 RMVar_ID_31312 Human_SNP_ID_9841662 A-to-I Human chr1 - 37688919 37688919 37688919 CTCTGTCACTCAGGCTGGAGTGCAGTGGCACAATCACAGCTCATTGTAGCCTCGATTTCCCTGGT CTCTGTCACTCAGGCTGGAGTGCAGTGGCACAGTCACAGCTCATTGTAGCCTCGATTTCCCTGGT T C C1orf109 Ensembl:ENSG00000116922 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1446860558 Functional Loss SNV dbSNP153 33..33 33 - - - 31313 RMVar_ID_31313 Human_SNP_ID_9843016 A-to-I Human chr1 + 37693538 37693538 37693538 CTCCTGCCTCAGCCTCTGGAGTGGCTGGGATTACGGTCGCCTGCCACCATGCCCCGCTGATTTTT CTCCTGCCTCAGCCTCTGGAGTGGCTGGGATTGCGGTCGCCTGCCACCATGCCCCGCTGATTTTT A G CDCA8 Ensembl:ENSG00000134690 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569991931 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_46843 31314 RMVar_ID_31314 Human_SNP_ID_9843031 A-to-I Human chr1 + 37693573 37693573 37693573 GTCGCCTGCCACCATGCCCCGCTGATTTTTGTATTTTCAGTAGAGACGGGGTTTCACCATGTTGG GTCGCCTGCCACCATGCCCCGCTGATTTTTGTGTTTTCAGTAGAGACGGGGTTTCACCATGTTGG A G CDCA8 Ensembl:ENSG00000134690 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1255723862 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_46843 31315 RMVar_ID_31315 Human_SNP_ID_9871511 A-to-I Human chr1 - 37806297 37806297 37806297 ACTTGGGAGGCTGAGGCAGGAGAATCACTTGAACCTGGGAGGCAGAGGTTACAGTGAGCTCAGAT ACTTGGGAGGCTGAGGCAGGAGAATCACTTGATCCTGGGAGGCAGAGGTTACAGTGAGCTCAGAT T A YRDC Ensembl:ENSG00000196449 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1246192294 Functional Loss SNV dbSNP153 33..33 33 - - - 31316 RMVar_ID_31316 Human_SNP_ID_9876827 A-to-I Human chr1 - 37826896 37826896 37826896 CAGCTCGCTGCAACCTCCACTTCCCAGGTTCAAGTAATTCTCCTGCCTCAGCGTCCCGAGTAGCT CAGCTCGCTGCAACCTCCACTTCCCAGGTTCAGGTAATTCTCCTGCCTCAGCGTCCCGAGTAGCT T C MTF1 Ensembl:ENSG00000188786 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1032512282 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12981,RMVar_hsa_circ_11497,RMVar_hsa_circ_373090,RMVar_hsa_circ_131752 31317 RMVar_ID_31317 Human_SNP_ID_9884877 A-to-I Human chr1 - 37860971 37860971 37860971 ATTTTTAAAAAATTAGCTGGGTGTGGTGATGCATGCCTGTGGTCCCAGTTACTTGGGAGGCTGAC ATTTTTAAAAAATTAGCTGGGTGTGGTGATGCGTGCCTGTGGTCCCAGTTACTTGGGAGGCTGAC T C INPP5B Ensembl:ENSG00000204084 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1136991 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17556632,Human_RBP_ID_26380057 31318 RMVar_ID_31318 Human_SNP_ID_9884889 A-to-I Human chr1 - 37861028 37861028 37861028 GACCAGGAGTTTGGGACCAGGCTGGGCAACACAGGGAGACCCCCTCTCTACAAAAACATTTTTAA GACCAGGAGTTTGGGACCAGGCTGGGCAACACGGGGAGACCCCCTCTCTACAAAAACATTTTTAA T C INPP5B Ensembl:ENSG00000204084 Protein coding 3'UTR GSE100210;GSE107867;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;ASD brains,frontal_cortex;ASD brains,temporal_cortex;Bronchiolar epithelium,BEP2D cell line - 29129909,30559470,30559470,31158229 RNA-Seq:(High) rs1350617002 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26385951 31319 RMVar_ID_31319 Human_SNP_ID_9884891 A-to-I Human chr1 - 37861033 37861033 37861033 CTTGAGACCAGGAGTTTGGGACCAGGCTGGGCAACACAGGGAGACCCCCTCTCTACAAAAACATT CTTGAGACCAGGAGTTTGGGACCAGGCTGGGCGACACAGGGAGACCCCCTCTCTACAAAAACATT T C INPP5B Ensembl:ENSG00000204084 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1136986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26385951 31320 RMVar_ID_31320 Human_SNP_ID_9884895 A-to-I Human chr1 - 37861056 37861056 37861056 GGGAGACTGAGGTGGGAGCATCACTTGAGACCAGGAGTTTGGGACCAGGCTGGGCAACACAGGGA GGGAGACTGAGGTGGGAGCATCACTTGAGACCGGGAGTTTGGGACCAGGCTGGGCAACACAGGGA T C INPP5B Ensembl:ENSG00000204084 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1136981 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26385951 31321 RMVar_ID_31321 Human_SNP_ID_9884905 A-to-I Human chr1 - 37861101 37861101 37861101 AAAATGACCAGGCACAGTGGCTCACGCCTGTAATCTCGGCACTTTGGGAGACTGAGGTGGGAGCA AAAATGACCAGGCACAGTGGCTCACGCCTGTAGTCTCGGCACTTTGGGAGACTGAGGTGGGAGCA T C INPP5B Ensembl:ENSG00000204084 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs3200623 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22558708,Human_RBP_ID_26385952 31322 RMVar_ID_31322 Human_SNP_ID_9884989 A-to-I Human chr1 - 37861459 37861459 37861459 GGCCTCCCAAAGTGCTGGGATTACAGGCATGAACCACCACGCCTGGCCTAAAATGTTTTTAAATA GGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCACGCCTGGCCTAAAATGTTTTTAAATA T C INPP5B Ensembl:ENSG00000204084 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1263490098 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26385955 31323 RMVar_ID_31323 Human_SNP_ID_9884990 A-to-I Human chr1 - 37861463 37861463 37861463 CCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAACCACCACGCCTGGCCTAAAATGTTTTTA CCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAACCACCACGCCTGGCCTAAAATGTTTTTA T C INPP5B Ensembl:ENSG00000204084 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE112787;GSE107867;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;293 Flip-In T-REx cells,empty vector;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,29129909,29967493,30559470,32596459 RNA-Seq:(High) rs1355476176 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26385955 31324 RMVar_ID_31324 Human_SNP_ID_9884997 A-to-I Human chr1 - 37861483 37861483 37861483 GGCCTCAGGTGATCCACCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAACCACCACG GGCCTCAGGTGATCCACCTGCCTTGGCCTCCCCAAGTGCTGGGATTACAGGCATGAACCACCACG T G INPP5B Ensembl:ENSG00000204084 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1481784316 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26385955 31325 RMVar_ID_31325 Human_SNP_ID_9885094 A-to-I Human chr1 - 37861785 37861785 37861785 GTAATCTGCCTGCCTCGGCCTCCCCAAGTGCTAGGATTACAGATGTGAGCCACCACGCCCGGCCT GTAATCTGCCTGCCTCGGCCTCCCCAAGTGCTGGGATTACAGATGTGAGCCACCACGCCCGGCCT T C INPP5B Ensembl:ENSG00000204084 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1339043641 Functional Loss SNV dbSNP153 33..33 33 - - - 31326 RMVar_ID_31326 Human_SNP_ID_9885099 A-to-I Human chr1 - 37861814 37861814 37861814 CCAGGCTGTTCTAAAACTCCTGAACTCAGGTAATCTGCCTGCCTCGGCCTCCCCAAGTGCTAGGA CCAGGCTGTTCTAAAACTCCTGAACTCAGGTATTCTGCCTGCCTCGGCCTCCCCAAGTGCTAGGA T A INPP5B Ensembl:ENSG00000204084 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs541317837 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10972900,Human_RBP_ID_26380060 31327 RMVar_ID_31327 Human_SNP_ID_9885100 A-to-I Human chr1 - 37861815 37861815 37861815 CCCAGGCTGTTCTAAAACTCCTGAACTCAGGTAATCTGCCTGCCTCGGCCTCCCCAAGTGCTAGG CCCAGGCTGTTCTAAAACTCCTGAACTCAGGTTATCTGCCTGCCTCGGCCTCCCCAAGTGCTAGG T A INPP5B Ensembl:ENSG00000204084 Protein coding 3'UTR GSE38233;GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,32596459 RNA-Seq:(High) rs970587922 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10972900,Human_RBP_ID_26380060 31328 RMVar_ID_31328 Human_SNP_ID_9885121 A-to-I Human chr1 - 37861906 37861906 37861906 TCAGCCTCCCGAGTAGCTGGGACTGCAGGCACACACTGCCACGCCCAGCTAATTTTTTGCATTTT TCAGCCTCCCGAGTAGCTGGGACTGCAGGCACGCACTGCCACGCCCAGCTAATTTTTTGCATTTT T C INPP5B Ensembl:ENSG00000204084 Protein coding 3'UTR GSE47997;GSE38233;GSE99789;GSE107867;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;esophageal squamous carcinoma cells,EC109;ASD brains,Fragile X samples from NIH NeuroBioBank;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,29796672,30559470,32596459 RNA-Seq:(High) rs1407039630 Functional Loss SNV dbSNP153 33..33 33 - - - 31329 RMVar_ID_31329 Human_SNP_ID_9888463 A-to-I Human chr1 - 37874757 37874757 37874757 GAGTCTTACTCTGTCACCCAGGCTGGAGTGCAATGGCACGATCTCGGCTCACTGCAACCTCCGCC GAGTCTTACTCTGTCACCCAGGCTGGAGTGCAGTGGCACGATCTCGGCTCACTGCAACCTCCGCC T C INPP5B Ensembl:ENSG00000204084 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1045688784 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_131759,RMVar_hsa_circ_90742,RMVar_hsa_circ_88783,RMVar_hsa_circ_131760,RMVar_hsa_circ_265083,RMVar_hsa_circ_343429,RMVar_hsa_circ_329049,RMVar_hsa_circ_350926,RMVar_hsa_circ_265711,RMVar_hsa_circ_131762,RMVar_hsa_circ_109609,RMVar_hsa_circ_311918 31330 RMVar_ID_31330 Human_SNP_ID_9888599 A-to-I Human chr1 - 37875400 37875400 37875400 GCCGGGCGTGGTGGTCGGCACCTGTAGTCCCAACTACTCGGGAGGCTGAGACAGGAGAATGACGT GCCGGGCGTGGTGGTCGGCACCTGTAGTCCCAGCTACTCGGGAGGCTGAGACAGGAGAATGACGT T C INPP5B Ensembl:ENSG00000204084 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs573827440 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_131759,RMVar_hsa_circ_90742,RMVar_hsa_circ_88783,RMVar_hsa_circ_131760,RMVar_hsa_circ_265083,RMVar_hsa_circ_343429,RMVar_hsa_circ_329049,RMVar_hsa_circ_350926,RMVar_hsa_circ_265711,RMVar_hsa_circ_131762,RMVar_hsa_circ_109609,RMVar_hsa_circ_311918 31331 RMVar_ID_31331 Human_SNP_ID_9888830 A-to-I Human chr1 - 37876206 37876206 37876206 TCAGCTACTTGGGGGGCTGAGGTAGGAGCATCACTTGAACCCAGAAGGCGGAGGTTGCAGTGAGC TCAGCTACTTGGGGGGCTGAGGTAGGAGCATCTCTTGAACCCAGAAGGCGGAGGTTGCAGTGAGC T A INPP5B Ensembl:ENSG00000204084 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1362246798 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61859,RMVar_hsa_circ_131759,RMVar_hsa_circ_90742,RMVar_hsa_circ_88783,RMVar_hsa_circ_131760,RMVar_hsa_circ_265083,RMVar_hsa_circ_343429,RMVar_hsa_circ_329049,RMVar_hsa_circ_350926,RMVar_hsa_circ_265711,RMVar_hsa_circ_131762,RMVar_hsa_circ_109609,RMVar_hsa_circ_323959,RMVar_hsa_circ_332950,RMVar_hsa_circ_358362,RMVar_hsa_circ_324008,RMVar_hsa_circ_81814,RMVar_hsa_circ_131763,RMVar_hsa_circ_131764 31332 RMVar_ID_31332 Human_SNP_ID_9889730 A-to-I Human chr1 - 37879642 37879642 37879642 GCGATTCTCCTGCCTCATCCTCCCAAGTAGCTAGGATTACAGGCATGTGCCACCAGGCCCAGCTA GCGATTCTCCTGCCTCATCCTCCCAAGTAGCTGGGATTACAGGCATGTGCCACCAGGCCCAGCTA T C INPP5B Ensembl:ENSG00000204084 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs779161969 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61859,RMVar_hsa_circ_88783,RMVar_hsa_circ_131760,RMVar_hsa_circ_343429,RMVar_hsa_circ_329049,RMVar_hsa_circ_350926,RMVar_hsa_circ_265711,RMVar_hsa_circ_131762,RMVar_hsa_circ_109609,RMVar_hsa_circ_332950,RMVar_hsa_circ_358362,RMVar_hsa_circ_324008,RMVar_hsa_circ_81814,RMVar_hsa_circ_131763,RMVar_hsa_circ_131764 31333 RMVar_ID_31333 Human_SNP_ID_9889749 A-to-I Human chr1 - 37879727 37879727 37879727 TTGAGACAGAGTCTTGCTCTGTCATCCAGGCTAGGGTACAATGGCTGGATCTTGGCCCACTGCAA TTGAGACAGAGTCTTGCTCTGTCATCCAGGCTGGGGTACAATGGCTGGATCTTGGCCCACTGCAA T C INPP5B Ensembl:ENSG00000204084 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs983512749 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61859,RMVar_hsa_circ_88783,RMVar_hsa_circ_131760,RMVar_hsa_circ_343429,RMVar_hsa_circ_329049,RMVar_hsa_circ_350926,RMVar_hsa_circ_265711,RMVar_hsa_circ_131762,RMVar_hsa_circ_109609,RMVar_hsa_circ_332950,RMVar_hsa_circ_358362,RMVar_hsa_circ_324008,RMVar_hsa_circ_81814,RMVar_hsa_circ_131763,RMVar_hsa_circ_131764 31334 RMVar_ID_31334 Human_SNP_ID_9890828 A-to-I Human chr1 - 37884569 37884569 37884569 AGAAATAAGAAGAAAGTGAGGCTGGGTGCAGTAGTTCATGCCTGTTATCCCAGCATTTTAGGAGG AGAAATAAGAAGAAAGTGAGGCTGGGTGCAGTGGTTCATGCCTGTTATCCCAGCATTTTAGGAGG T C INPP5B Ensembl:ENSG00000204084 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1270216869 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557125,Human_RBP_ID_22562925 RMVar_hsa_circ_61859,RMVar_hsa_circ_88783,RMVar_hsa_circ_131760,RMVar_hsa_circ_343429,RMVar_hsa_circ_265711,RMVar_hsa_circ_332950,RMVar_hsa_circ_358362,RMVar_hsa_circ_81814,RMVar_hsa_circ_131766,RMVar_hsa_circ_108438,RMVar_hsa_circ_131764,RMVar_hsa_circ_296858,RMVar_hsa_circ_347455,RMVar_hsa_circ_36098,RMVar_hsa_circ_337000,RMVar_hsa_circ_131765,RMVar_hsa_circ_131767 31335 RMVar_ID_31335 Human_SNP_ID_9905771 A-to-I Human chr1 - 37942717 37942717 37942717 TTCTGCAGAGGCGGGGTTTTGCCATGTTGGCCAGGCTGGTCTTGAACTCCTGACCTCAGATGATC TTCTGCAGAGGCGGGGTTTTGCCATGTTGGCCGGGCTGGTCTTGAACTCCTGACCTCAGATGATC T C INPP5B Ensembl:ENSG00000204084 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1406399718 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_343429,RMVar_hsa_circ_81814,RMVar_hsa_circ_131764,RMVar_hsa_circ_36098,RMVar_hsa_circ_84168,RMVar_hsa_circ_131768,RMVar_hsa_circ_349004 31336 RMVar_ID_31336 Human_SNP_ID_9909410 A-to-I Human chr1 - 37957407 37957406 37957407 TGAGACCAGCCTGGGCGATATAGTGAGGCCCCATCTCAAAAAAAAAAAAAGGGGGGGGGGGGGGA TGAGACCAGCCTGGGCGATATAGTGAGGCCCC_TCTCAAAAAAAAAAAAAGGGGGGGGGGGGGGA AT A SF3A3 Ensembl:ENSG00000183431 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1557744328 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_22875111,Human_RBP_ID_24694030,Human_RBP_ID_26380071 31337 RMVar_ID_31337 Human_SNP_ID_9910243 A-to-I Human chr1 - 37960868 37960868 37960868 CGGGTGGATCACGAGGTCAGGAGATGGAGACCATCCTGGCTAACACGGTGAAACCCCATCTCTAC CGGGTGGATCACGAGGTCAGGAGATGGAGACCGTCCTGGCTAACACGGTGAAACCCCATCTCTAC T C SF3A3 Ensembl:ENSG00000183431 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1269069067 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14763,RMVar_hsa_circ_112789,RMVar_hsa_circ_131776 31338 RMVar_ID_31338 Human_SNP_ID_9911257 A-to-I Human chr1 - 37963996 37963996 37963996 TTTTGTATTTTTAGTAGGGATGGGGTTTCACCATGCTGGCCAAGATGGTCTTGATCTCTGACCTC TTTTGTATTTTTAGTAGGGATGGGGTTTCACCGTGCTGGCCAAGATGGTCTTGATCTCTGACCTC T C SF3A3 Ensembl:ENSG00000183431 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs914229850 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10973742 RMVar_hsa_circ_14763,RMVar_hsa_circ_112789,RMVar_hsa_circ_131776 31339 RMVar_ID_31339 Human_SNP_ID_9911258 A-to-I Human chr1 - 37963996 37963996 37963996 TTTTGTATTTTTAGTAGGGATGGGGTTTCACCATGCTGGCCAAGATGGTCTTGATCTCTGACCTC TTTTGTATTTTTAGTAGGGATGGGGTTTCACCCTGCTGGCCAAGATGGTCTTGATCTCTGACCTC T G SF3A3 Ensembl:ENSG00000183431 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs914229850 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10973742 RMVar_hsa_circ_14763,RMVar_hsa_circ_112789,RMVar_hsa_circ_131776 31340 RMVar_ID_31340 Human_SNP_ID_9911438 A-to-I Human chr1 - 37964556 37964556 37964556 TCAACCAGGCTGGAGTGCAGTGGCGTGATCTCAGCTCACTGCAATCTCCACCTCCTGGTTCCAAG TCAACCAGGCTGGAGTGCAGTGGCGTGATCTCTGCTCACTGCAATCTCCACCTCCTGGTTCCAAG T A SF3A3 Ensembl:ENSG00000183431 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1184162066 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14763,RMVar_hsa_circ_112789,RMVar_hsa_circ_131776 31341 RMVar_ID_31341 Human_SNP_ID_9916468 A-to-I Human chr1 - 37983717 37983717 37983717 TTGCCCAGGCTGGTCACAAACTCCTGACCTCAAATGATCCTCCTGTCTCGGCCTCCCACAGTGTT TTGCCCAGGCTGGTCACAAACTCCTGACCTCAGATGATCCTCCTGTCTCGGCCTCCCACAGTGTT T C SF3A3 Ensembl:ENSG00000183431 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1385936998 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24694118 RMVar_hsa_circ_16091,RMVar_hsa_circ_11584,RMVar_hsa_circ_105339,RMVar_hsa_circ_365433,RMVar_hsa_circ_60792,RMVar_hsa_circ_131778,RMVar_hsa_circ_131780,RMVar_hsa_circ_81684,RMVar_hsa_circ_373057,RMVar_hsa_circ_79515,RMVar_hsa_circ_131779,RMVar_hsa_circ_353288,RMVar_hsa_circ_74322,RMVar_hsa_circ_131781,RMVar_hsa_circ_301309,RMVar_hsa_circ_322950 31342 RMVar_ID_31342 Human_SNP_ID_9918436 A-to-I Human chr1 - 37990579 37990579 37990579 TGTTTTTAGTAGAGACGGGGTTTCACCATGTTAGCCAGCCTGGTCGTCTCGAACCTCTGACCTCA TGTTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGCCTGGTCGTCTCGAACCTCTGACCTCA T C - - Other Unknown GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1322311997 Functional Loss SNV dbSNP153 33..33 33 - - - 31343 RMVar_ID_31343 Human_SNP_ID_9919306 A-to-I Human chr1 - 37993685 37993685 37993685 ATGAGGTCTCGCTATGTTGCCCAGACTGTTCTAGAACTCCTGGCTTTAAGCGAAATTCCCAGCTT ATGAGGTCTCGCTATGTTGCCCAGACTGTTCTGGAACTCCTGGCTTTAAGCGAAATTCCCAGCTT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs951531836 Functional Loss SNV dbSNP153 33..33 33 - - - 31344 RMVar_ID_31344 Human_SNP_ID_9927341 A-to-I Human chr1 + 38022751 38022751 38022751 AAAGCAGTATAACTGCCTGACACAGCGGATTGAACGAGAGAAGAAATTGTTCGTTATTGCTCAGA AAAGCAGTATAACTGCCTGACACAGCGGATTGCACGAGAGAAGAAATTGTTCGTTATTGCTCAGA A C UTP11 Ensembl:ENSG00000183520 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1361357826 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1431181,Human_RBP_ID_1747412,Human_RBP_ID_10974629,Human_RBP_ID_22430466,Human_RBP_ID_23392958,Human_RBP_ID_27182857 Human_Splice_Rec_49500,Human_Splice_Rec_49501,Human_Splice_Rec_49510,Human_Splice_Rec_49511 31345 RMVar_ID_31345 Human_SNP_ID_10087293 A-to-I Human chr1 + 38709518 38709518 38709518 TTGCTGACCTAAATGTTATGAGGATCATCAATAAGCCTACAGCAGCTGCTATTGCTTATGGCCTG TTGCTGACCTAAATGTTATGAGGATCATCAATGAGCCTACAGCAGCTGCTATTGCTTATGGCCTG A G HSPA5P1 Ensembl:ENSG00000215895 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878915998 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1876494 31346 RMVar_ID_31346 Human_SNP_ID_10087298 A-to-I Human chr1 + 38709526 38709526 38709526 CTAAATGTTATGAGGATCATCAATAAGCCTACAGCAGCTGCTATTGCTTATGGCCTGGATAAGAG CTAAATGTTATGAGGATCATCAATAAGCCTACGGCAGCTGCTATTGCTTATGGCCTGGATAAGAG A G HSPA5P1 Ensembl:ENSG00000215895 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs766464340 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8242510 Human_miRNA_ID_1870297,Human_miRNA_ID_1876302,Human_miRNA_ID_1876494,Human_miRNA_ID_1878549 31347 RMVar_ID_31347 Human_SNP_ID_10119043 A-to-I Human chr1 - 38848797 38848797 38848797 ACTTTTTTGTAGAGACAGGGTCTCATAGTGTTACCCAGGCTGGTATCGAACTCCTGGCCTTAAGC ACTTTTTTGTAGAGACAGGGTCTCATAGTGTTGCCCAGGCTGGTATCGAACTCCTGGCCTTAAGC T C AL139260.2,RRAGC Ensembl:ENSG00000273637,Ensembl:ENSG00000116954 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355945119 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10976407 RMVar_hsa_circ_73604 31348 RMVar_ID_31348 Human_SNP_ID_10119178 A-to-I Human chr1 - 38849295 38849295 38849295 TAAATTTGGGGGATTAAGCAGAAGGATGAGGCAGGAGAATTACTTGATCCCAGGAGTTCCAGGCT TAAATTTGGGGGATTAAGCAGAAGGATGAGGCTGGAGAATTACTTGATCCCAGGAGTTCCAGGCT T A AL139260.2,RRAGC Ensembl:ENSG00000273637,Ensembl:ENSG00000116954 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1029546707 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73604 31349 RMVar_ID_31349 Human_SNP_ID_10119179 A-to-I Human chr1 - 38849295 38849295 38849295 TAAATTTGGGGGATTAAGCAGAAGGATGAGGCAGGAGAATTACTTGATCCCAGGAGTTCCAGGCT TAAATTTGGGGGATTAAGCAGAAGGATGAGGCGGGAGAATTACTTGATCCCAGGAGTTCCAGGCT T C AL139260.2,RRAGC Ensembl:ENSG00000273637,Ensembl:ENSG00000116954 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1029546707 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73604 31350 RMVar_ID_31350 Human_SNP_ID_10122687 A-to-I Human chr1 + 38861905 38861901 38861905 GGGGTTCCACCATGTTGGCCAGGATGGTTTCTATCTCTTGACCTCAAGATCCACCCTCCATGGCC GGGGTTCCACCATGTTGGCCAGGATGGTT____TCTCTTGACCTCAAGATCCACCCTCCATGGCC TTCTA T AL139260.1 Ensembl:ENSG00000228436 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355869692 Functional Loss DEL dbSNP153 30..33 33 - - - 31351 RMVar_ID_31351 Human_SNP_ID_10123014 A-to-I Human chr1 - 38863663 38863663 38863663 AGGCCAAAGACTGATATTAATACAAATCACTCACTAACTGTAGAGCCTTGGGCATTATCAGTGAA AGGCCAAAGACTGATATTAATACAAATCACTCCCTAACTGTAGAGCCTTGGGCATTATCAGTGAA T G MYCBP,AL139260.2 Ensembl:ENSG00000214114,Ensembl:ENSG00000273637 Protein coding,lincRNA 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1050468 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_354749,Human_RBP_ID_978200,Human_RBP_ID_1431220,Human_RBP_ID_1747439,Human_RBP_ID_5821453,Human_RBP_ID_8048688,Human_RBP_ID_10976509,Human_RBP_ID_16975803,Human_RBP_ID_17218465,Human_RBP_ID_17335759,Human_RBP_ID_17452991,Human_RBP_ID_17750681,Human_RBP_ID_18230224,Human_RBP_ID_21909971,Human_RBP_ID_22420124,Human_RBP_ID_23262208,Human_RBP_ID_23393222,Human_RBP_ID_26385967,Human_RBP_ID_27398612,Human_RBP_ID_27594373 31352 RMVar_ID_31352 Human_SNP_ID_10132856 A-to-I Human chr1 + 38901201 38901201 38901201 TATCAGGCATATGGTCGGCTGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGACAAGGC TATCAGGCATATGGTCGGCTGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGACAAGGC A G AL139260.1 Ensembl:ENSG00000228436 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1163920026 Functional Loss SNV dbSNP153 33..33 33 - - - 31353 RMVar_ID_31353 Human_SNP_ID_10133956 A-to-I Human chr1 + 38905274 38905274 38905274 TTTGGTAGAGACAGAGTTTCATTATATTGCCCAGGCTGGTCTCAAACTACTGAACTCAGGCAATC TTTGGTAGAGACAGAGTTTCATTATATTGCCCGGGCTGGTCTCAAACTACTGAACTCAGGCAATC A G AL139260.1 Ensembl:ENSG00000228436 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1434829423 Functional Loss SNV dbSNP153 33..33 33 - - - 31354 RMVar_ID_31354 Human_SNP_ID_10157399 A-to-I Human chr1 + 38993352 38993352 38993352 GGGTGGATCAAGAGACCGAGACCATCCTGGCCAACATGGTGAAAACCCTGTTTCTACTAAAAATA GGGTGGATCAAGAGACCGAGACCATCCTGGCCGACATGGTGAAAACCCTGTTTCTACTAAAAATA A G AKIRIN1 Ensembl:ENSG00000174574 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042125662 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8310643 31355 RMVar_ID_31355 Human_SNP_ID_10157548 A-to-I Human chr1 + 38993757 38993754 38993757 GCCCAGGAATTCGAGACAAGTCTGTGCAACATAATGAGACCTTGTTTCCACAAAAGAATTCTAAG GCCCAGGAATTCGAGACAAGTCTGTGCAAC___ATGAGACCTTGTTTCCACAAAAGAATTCTAAG CATA C AKIRIN1 Ensembl:ENSG00000174574 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs376001785 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_10976825 31356 RMVar_ID_31356 Human_SNP_ID_10157569 A-to-I Human chr1 + 38993813 38993813 38993813 AATTCTAAGGCCGGGCGCAGTGGCTCACTCCTATAATCCCAGCACTTTGGGAGGCGGAGGCGGGC AATTCTAAGGCCGGGCGCAGTGGCTCACTCCTGTAATCCCAGCACTTTGGGAGGCGGAGGCGGGC A G AKIRIN1 Ensembl:ENSG00000174574 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270587198 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5821571,Human_RBP_ID_10976826 31357 RMVar_ID_31357 Human_SNP_ID_10157808 A-to-I Human chr1 + 38994623 38994623 38994623 CGTCTCCCATGTTCAAGCGATTCTCCTGCCTCAGCCTCCCCAGTGGCTGGGATTACAGGCATGTG CGTCTCCCATGTTCAAGCGATTCTCCTGCCTCGGCCTCCCCAGTGGCTGGGATTACAGGCATGTG A G AKIRIN1 Ensembl:ENSG00000174574 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1434523578 Functional Loss SNV dbSNP153 33..33 33 - - - 31358 RMVar_ID_31358 Human_SNP_ID_10157903 A-to-I Human chr1 + 38994764 38994764 38994764 CAGGCTGGAGTGCAGTAGCATGATCTCGGCTCACTGCAACTTCCACCTCCCAGACTCAAGCGATT CAGGCTGGAGTGCAGTAGCATGATCTCGGCTCTCTGCAACTTCCACCTCCCAGACTCAAGCGATT A T AKIRIN1 Ensembl:ENSG00000174574 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935437949 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10976875 31359 RMVar_ID_31359 Human_SNP_ID_10158016 A-to-I Human chr1 + 38995181 38995181 38995181 AGCAATAGTCCCATTTCGAGCACAGGGAAACCATGAGAGCAAAGTCCAAAAAACCCACAATTTAA AGCAATAGTCCCATTTCGAGCACAGGGAAACCGTGAGAGCAAAGTCCAAAAAACCCACAATTTAA A G AKIRIN1 Ensembl:ENSG00000174574 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6660176 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_3504,GWAS_ID_3505,GWAS_ID_3506,GWAS_ID_3507 31360 RMVar_ID_31360 Human_SNP_ID_10158206 A-to-I Human chr1 + 38995879 38995879 38995879 ACATTGTGAAACTCTGTCTCTACTAAAAATACAAAAAATTAGGTGGGTGTGGTGGCGGGCTCCTG ACATTGTGAAACTCTGTCTCTACTAAAAATACGAAAAATTAGGTGGGTGTGGTGGCGGGCTCCTG A G AKIRIN1 Ensembl:ENSG00000174574 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1044094387 Functional Loss SNV dbSNP153 33..33 33 - - - 31361 RMVar_ID_31361 Human_SNP_ID_10158207 A-to-I Human chr1 + 38995887 38995887 38995887 AAACTCTGTCTCTACTAAAAATACAAAAAATTAGGTGGGTGTGGTGGCGGGCTCCTGAAATCCAA AAACTCTGTCTCTACTAAAAATACAAAAAATTCGGTGGGTGTGGTGGCGGGCTCCTGAAATCCAA A C AKIRIN1 Ensembl:ENSG00000174574 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs554337046 Functional Loss SNV dbSNP153 33..33 33 - - - 31362 RMVar_ID_31362 Human_SNP_ID_10158213 A-to-I Human chr1 + 38995918 38995918 38995918 TAGGTGGGTGTGGTGGCGGGCTCCTGAAATCCAAACTACTCTGGAGGCTGAGGCAGGAGAATTGC TAGGTGGGTGTGGTGGCGGGCTCCTGAAATCCGAACTACTCTGGAGGCTGAGGCAGGAGAATTGC A G AKIRIN1 Ensembl:ENSG00000174574 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1208125691 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10976928,Human_RBP_ID_17557126 31363 RMVar_ID_31363 Human_SNP_ID_10158229 A-to-I Human chr1 + 38995966 38995966 38995966 TGAGGCAGGAGAATTGCTTGAACCTGGGAGGTAGAGGTTGCAGTGAACTGAGATTGTGCTATTGC TGAGGCAGGAGAATTGCTTGAACCTGGGAGGTGGAGGTTGCAGTGAACTGAGATTGTGCTATTGC A G AKIRIN1 Ensembl:ENSG00000174574 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1028524382 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557126 31364 RMVar_ID_31364 Human_SNP_ID_10158247 A-to-I Human chr1 + 38996021 38996021 38996021 GTGCTATTGCACTACAGCCTGGGCGACAGGGTAAGACTCTCTTAAAAAATAAAGTGAGGTGAAAA GTGCTATTGCACTACAGCCTGGGCGACAGGGTGAGACTCTCTTAAAAAATAAAGTGAGGTGAAAA A G AKIRIN1 Ensembl:ENSG00000174574 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs919855306 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5821600,Human_RBP_ID_17557126,Human_RBP_ID_23149509 31365 RMVar_ID_31365 Human_SNP_ID_10158303 A-to-I Human chr1 + 38996234 38996234 38996234 CTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGTGCGCACCACCATGCCCAGCTAATTTTT CTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTGCAGGTGCGCACCACCATGCCCAGCTAATTTTT A G AKIRIN1 Ensembl:ENSG00000174574 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1200020137 Functional Loss SNV dbSNP153 33..33 33 - - - 31366 RMVar_ID_31366 Human_SNP_ID_10158310 A-to-I Human chr1 + 38996260 38996260 38996260 GGGATTACAGGTGCGCACCACCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGATGGTTTCGCC GGGATTACAGGTGCGCACCACCATGCCCAGCTGATTTTTGTATTTTTAGTAGAGATGGTTTCGCC A G AKIRIN1 Ensembl:ENSG00000174574 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1282858259 Functional Loss SNV dbSNP153 33..33 33 - - - 31367 RMVar_ID_31367 Human_SNP_ID_10158313 A-to-I Human chr1 + 38996275 38996275 38996275 CACCACCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGATGGTTTCGCCATGTTGGTCAGGCTG CACCACCATGCCCAGCTAATTTTTGTATTTTTGGTAGAGATGGTTTCGCCATGTTGGTCAGGCTG A G AKIRIN1 Ensembl:ENSG00000174574 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1447668468 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24694407 31368 RMVar_ID_31368 Human_SNP_ID_10158434 A-to-I Human chr1 + 38996714 38996714 38996714 ACCACGCCTGGCTAAATTTTTTTATTTTTAGTAGAGACGGTGTTTCACCATGTTAGCCAAGATAG ACCACGCCTGGCTAAATTTTTTTATTTTTAGTGGAGACGGTGTTTCACCATGTTAGCCAAGATAG A G AKIRIN1 Ensembl:ENSG00000174574 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1461976313 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10976957 31369 RMVar_ID_31369 Human_SNP_ID_10158438 A-to-I Human chr1 + 38996728 38996728 38996728 AATTTTTTTATTTTTAGTAGAGACGGTGTTTCACCATGTTAGCCAAGATAGTCTCGATTTCATGA AATTTTTTTATTTTTAGTAGAGACGGTGTTTCGCCATGTTAGCCAAGATAGTCTCGATTTCATGA A G AKIRIN1 Ensembl:ENSG00000174574 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1384974624 Functional Loss SNV dbSNP153 33..33 33 - - - 31370 RMVar_ID_31370 Human_SNP_ID_10158444 A-to-I Human chr1 + 38996740 38996740 38996740 TTTAGTAGAGACGGTGTTTCACCATGTTAGCCAAGATAGTCTCGATTTCATGACCTTGTGATCTG TTTAGTAGAGACGGTGTTTCACCATGTTAGCCGAGATAGTCTCGATTTCATGACCTTGTGATCTG A G AKIRIN1 Ensembl:ENSG00000174574 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs757156016 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10976958 31371 RMVar_ID_31371 Human_SNP_ID_10158455 A-to-I Human chr1 + 38996789 38996789 38996789 ATGACCTTGTGATCTGCCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATAAGCCACCATA ATGACCTTGTGATCTGCCTGCCTCAGCCTCCCGAAGTGCTGGGATTACAGGCATAAGCCACCATA A G AKIRIN1 Ensembl:ENSG00000174574 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs757948657 Functional Loss SNV dbSNP153 33..33 33 - - - 31372 RMVar_ID_31372 Human_SNP_ID_10158456 A-to-I Human chr1 + 38996790 38996790 38996790 TGACCTTGTGATCTGCCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATAAGCCACCATAC TGACCTTGTGATCTGCCTGCCTCAGCCTCCCAGAGTGCTGGGATTACAGGCATAAGCCACCATAC A G AKIRIN1 Ensembl:ENSG00000174574 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs987135667 Functional Loss SNV dbSNP153 33..33 33 - - - 31373 RMVar_ID_31373 Human_SNP_ID_10159795 A-to-I Human chr1 + 39001449 39001448 39001450 CCATGCCTGGCTAATTTTTTTGTATTTTTAGCAGAGAGGGGGCTTCTCCATGTTTGTCAGGCTGG CCATGCCTGGCTAATTTTTTTGTATTTTTAGC__AGAGGGGGCTTCTCCATGTTTGTCAGGCTGG CAG C AKIRIN1 Ensembl:ENSG00000174574 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1156475851 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_10977175 RMVar_hsa_circ_16000 31374 RMVar_ID_31374 Human_SNP_ID_10160091 A-to-I Human chr1 + 39002475 39002475 39002475 GGTCTAGGCCGGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCAG GGTCTAGGCCGGGCGCAGTGGCTCACGCCTGTGATCCCAGCACTTTGGGAGGCCGAGGCGGGCAG A G AKIRIN1 Ensembl:ENSG00000174574 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs542271620 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16000 31375 RMVar_ID_31375 Human_SNP_ID_10167436 A-to-I Human chr1 + 39029086 39029085 39029086 GCCACCTCGTCTCACTGTAGCCTCTGCCTCCCAGGTTCAGGCGATTCGCGTACCTCAGCCTCCCG GCCACCTCGTCTCACTGTAGCCTCTGCCTCCC_GGTTCAGGCGATTCGCGTACCTCAGCCTCCCG CA C NDUFS5 Ensembl:ENSG00000168653 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1157143413 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_113812,RMVar_hsa_circ_131807 31376 RMVar_ID_31376 Human_SNP_ID_10167850 A-to-I Human chr1 + 39030584 39030584 39030584 AAAAAATTAGCTGGGTGTAGTGGCTGGCGCCTATAGTCCCAGCTACTCGGGAGGCTGAGGCAGGA AAAAAATTAGCTGGGTGTAGTGGCTGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGA A G NDUFS5 Ensembl:ENSG00000168653 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1170245062 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113812,RMVar_hsa_circ_131807 31377 RMVar_ID_31377 Human_SNP_ID_10168653 A-to-I Human chr1 + 39033990 39033990 39033990 CCCTGGCTAATTTTTGTATTTTTAGTAGAAACAAGGTTTTACCTTGTTGGCCAGTCTGGTCTTAA CCCTGGCTAATTTTTGTATTTTTAGTAGAAACGAGGTTTTACCTTGTTGGCCAGTCTGGTCTTAA A G NDUFS5 Ensembl:ENSG00000168653 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1199098604 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113812,RMVar_hsa_circ_131807 31378 RMVar_ID_31378 Human_SNP_ID_10170405 A-to-I Human chr1 + 39040255 39040255 39040255 CCACCATGCCCGGCGAATTTTGTATTTTTAGTAGAGACGGGGTTTCTCCATGTTGGTCAGGGTGG CCACCATGCCCGGCGAATTTTGTATTTTTAGTGGAGACGGGGTTTCTCCATGTTGGTCAGGGTGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202631810 Functional Loss SNV dbSNP153 33..33 33 - - - 31379 RMVar_ID_31379 Human_SNP_ID_10173585 A-to-I Human chr1 + 39051972 39051972 39051972 TTTGTATTTTTAGTAAAGACAGGAGTTTCACCATATTGGCCAGGTTGGTCTCGAACTCATGACCT TTTGTATTTTTAGTAAAGACAGGAGTTTCACCGTATTGGCCAGGTTGGTCTCGAACTCATGACCT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1382727786 Functional Loss SNV dbSNP153 33..33 33 - - - 31380 RMVar_ID_31380 Human_SNP_ID_10175643 A-to-I Human chr1 + 39060743 39060743 39060743 GTGGTGGCAGGTGCTTGTGGTCCCAGCTACTCAGGAGGCTGAGGCGGGAGAATGACATGAATCTG GTGGTGGCAGGTGCTTGTGGTCCCAGCTACTCGGGAGGCTGAGGCGGGAGAATGACATGAATCTG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1245002100 Functional Loss SNV dbSNP153 33..33 33 - - - 31381 RMVar_ID_31381 Human_SNP_ID_10191421 A-to-I Human chr1 + 39122332 39122332 39122332 GCTGGAGTACAGTGGCGCGATGTCGGCTCACTACAACCTCTGCCTCCTGGATTCAAGCAATTCTG GCTGGAGTACAGTGGCGCGATGTCGGCTCACTGCAACCTCTGCCTCCTGGATTCAAGCAATTCTG A G MACF1 Ensembl:ENSG00000127603 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1557467144 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 31382 RMVar_ID_31382 Human_SNP_ID_10198209 A-to-I Human chr1 + 39151992 39151992 39151992 TTATAAAATATATATATTTTTTATTTTTTTTTAAGACGGAGTTTTGCTCTTGTTACCTAGGCTGG TTATAAAATATATATATTTTTTATTTTTTTTTGAGACGGAGTTTTGCTCTTGTTACCTAGGCTGG A G MACF1 Ensembl:ENSG00000127603 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1489781840 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 31383 RMVar_ID_31383 Human_SNP_ID_10210497 A-to-I Human chr1 + 39203315 39203315 39203315 AGCCTTGATTCCTGGGCTCAAGCCATCTTCCCACCTCAGCCTCCCCAGTAGCTGGGACTATACAC AGCCTTGATTCCTGGGCTCAAGCCATCTTCCCGCCTCAGCCTCCCCAGTAGCTGGGACTATACAC A G MACF1 Ensembl:ENSG00000127603 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs962088532 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 31384 RMVar_ID_31384 Human_SNP_ID_10243907 A-to-I Human chr1 + 39339180 39339167 39339180 GGAAGCTGAGGCAGGAGGATTTGCCTGAGCCCAGGAGTTTGAGGTTGTATTGAGCTATGAATGCA GGAAGCTGAGGCAGGAGGAT_____________GGAGTTTGAGGTTGTATTGAGCTATGAATGCA TTTGCCTGAGCCCA T MACF1 Ensembl:ENSG00000127603 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474793149 Functional Loss DEL dbSNP153 21..33 33 - - - RMVar_hsa_circ_44906,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_101311,RMVar_hsa_circ_131833,RMVar_hsa_circ_131834,RMVar_hsa_circ_131836,RMVar_hsa_circ_90817,RMVar_hsa_circ_70111,RMVar_hsa_circ_131841,RMVar_hsa_circ_131842,RMVar_hsa_circ_59788,RMVar_hsa_circ_57604,RMVar_hsa_circ_84174,RMVar_hsa_circ_131853,RMVar_hsa_circ_119605,RMVar_hsa_circ_5643,RMVar_hsa_circ_131856,RMVar_hsa_circ_3809,RMVar_hsa_circ_321276,RMVar_hsa_circ_366096,RMVar_hsa_circ_51881,RMVar_hsa_circ_84193,RMVar_hsa_circ_131863,RMVar_hsa_circ_131862,RMVar_hsa_circ_93350,RMVar_hsa_circ_100493,RMVar_hsa_circ_131864,RMVar_hsa_circ_131865,RMVar_hsa_circ_282073,RMVar_hsa_circ_110152,RMVar_hsa_circ_41034,RMVar_hsa_circ_131868,RMVar_hsa_circ_131867,RMVar_hsa_circ_124577,RMVar_hsa_circ_357492,RMVar_hsa_circ_313905,RMVar_hsa_circ_131873,RMVar_hsa_circ_131874,RMVar_hsa_circ_131872,RMVar_hsa_circ_299647,RMVar_hsa_circ_341288,RMVar_hsa_circ_363925,RMVar_hsa_circ_355162,RMVar_hsa_circ_323102,RMVar_hsa_circ_291997,RMVar_hsa_circ_293576,RMVar_hsa_circ_57154,RMVar_hsa_circ_131878,RMVar_hsa_circ_131880,RMVar_hsa_circ_131879,RMVar_hsa_circ_131876,RMVar_hsa_circ_131877,RMVar_hsa_circ_131875,RMVar_hsa_circ_2656,RMVar_hsa_circ_35444,RMVar_hsa_circ_45383,RMVar_hsa_circ_320387,RMVar_hsa_circ_321044,RMVar_hsa_circ_48984,RMVar_hsa_circ_42869,RMVar_hsa_circ_20943,RMVar_hsa_circ_131886 31385 RMVar_ID_31385 Human_SNP_ID_10251956 A-to-I Human chr1 + 39371229 39371229 39371229 TAATCCCAGCTACTCAAGAGGGTGAGGCAGAGAATTGCTTGAACTTGGGAGGTGGAGGTTGCAGT TAATCCCAGCTACTCAAGAGGGTGAGGCAGAGGATTGCTTGAACTTGGGAGGTGGAGGTTGCAGT A G MACF1 Ensembl:ENSG00000127603 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs543169934 Functional Loss SNV dbSNP153 33..33 33 - - - 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_101311,RMVar_hsa_circ_131833,RMVar_hsa_circ_131834,RMVar_hsa_circ_131836,RMVar_hsa_circ_90817,RMVar_hsa_circ_70111,RMVar_hsa_circ_131841,RMVar_hsa_circ_131842,RMVar_hsa_circ_59788,RMVar_hsa_circ_57604,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_131862,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_355162,RMVar_hsa_circ_323102,RMVar_hsa_circ_131875,RMVar_hsa_circ_2656,RMVar_hsa_circ_48984,RMVar_hsa_circ_42869,RMVar_hsa_circ_311189,RMVar_hsa_circ_351155,RMVar_hsa_circ_127892,RMVar_hsa_circ_293412,RMVar_hsa_circ_356814,RMVar_hsa_circ_65530,RMVar_hsa_circ_131895,RMVar_hsa_circ_131896,RMVar_hsa_circ_28963,RMVar_hsa_circ_359051,RMVar_hsa_circ_78655,RMVar_hsa_circ_93167,RMVar_hsa_circ_96358,RMVar_hsa_circ_131899,RMVar_hsa_circ_115324,RMVar_hsa_circ_131901,RMVar_hsa_circ_131902,RMVar_hsa_circ_131903,RMVar_hsa_circ_305247,RMVar_hsa_circ_361308,RMVar_hsa_circ_29980,RMVar_hsa_circ_131908,RMVar_hsa_circ_131907,RMVar_hsa_circ_351511,RMVar_hsa_circ_323258,RMVar_hsa_circ_29082,RMVar_hsa_circ_291625,RMVar_hsa_circ_131909,RMVar_hsa_circ_131910,RMVar_hsa_circ_79999,RMVar_hsa_circ_275812,RMVar_hsa_circ_335727,RMVar_hsa_circ_109098,RMVar_hsa_circ_131912,RMVar_hsa_circ_50750,RMVar_hsa_circ_131913,RMVar_hsa_circ_131911 31386 RMVar_ID_31386 Human_SNP_ID_10253327 A-to-I Human chr1 + 39376769 39376769 39376769 ACAGGGTCTCGCTCTGTCACCCAGGCTGGAGTACGGTAGTGTGATCATGGCTCTCTGTAGCTTTG ACAGGGTCTCGCTCTGTCACCCAGGCTGGAGTGCGGTAGTGTGATCATGGCTCTCTGTAGCTTTG A G MACF1 Ensembl:ENSG00000127603 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1345560153 Functional Loss SNV dbSNP153 33..33 33 - - - 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_101311,RMVar_hsa_circ_131833,RMVar_hsa_circ_131834,RMVar_hsa_circ_131836,RMVar_hsa_circ_90817,RMVar_hsa_circ_70111,RMVar_hsa_circ_131841,RMVar_hsa_circ_131842,RMVar_hsa_circ_59788,RMVar_hsa_circ_57604,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_2656,RMVar_hsa_circ_48984,RMVar_hsa_circ_311189,RMVar_hsa_circ_127892,RMVar_hsa_circ_356814,RMVar_hsa_circ_65530,RMVar_hsa_circ_131896,RMVar_hsa_circ_359051,RMVar_hsa_circ_78655,RMVar_hsa_circ_96358,RMVar_hsa_circ_131899,RMVar_hsa_circ_115324,RMVar_hsa_circ_131901,RMVar_hsa_circ_131902,RMVar_hsa_circ_361308,RMVar_hsa_circ_29980,RMVar_hsa_circ_4832,RMVar_hsa_circ_131907,RMVar_hsa_circ_351511,RMVar_hsa_circ_323258,RMVar_hsa_circ_29082,RMVar_hsa_circ_131909,RMVar_hsa_circ_131910,RMVar_hsa_circ_79999,RMVar_hsa_circ_335727,RMVar_hsa_circ_109098,RMVar_hsa_circ_131912,RMVar_hsa_circ_50750,RMVar_hsa_circ_131913,RMVar_hsa_circ_378249,RMVar_hsa_circ_300006,RMVar_hsa_circ_131914,RMVar_hsa_circ_131915 31387 RMVar_ID_31387 Human_SNP_ID_10258870 A-to-I Human chr1 + 39398313 39398313 39398313 GGTGCATGCTGCCATTCCTGGCTAATTTTTGTATTTTTTGTAGAGATAGAGTTTCACCATGTTGC GGTGCATGCTGCCATTCCTGGCTAATTTTTGTTTTTTTTGTAGAGATAGAGTTTCACCATGTTGC A T MACF1 Ensembl:ENSG00000127603 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs919232554 Functional Loss SNV dbSNP153 33..33 33 - - - 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 31388 RMVar_ID_31388 Human_SNP_ID_10260207 A-to-I Human chr1 + 39404351 39404351 39404351 AAATTAGCTGGGCATGGTGGTGCACACCTGTCATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAA AAATTAGCTGGGCATGGTGGTGCACACCTGTCGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAA A G MACF1 Ensembl:ENSG00000127603 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1319469923 Functional Loss SNV dbSNP153 33..33 33 - - - 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 31389 RMVar_ID_31389 Human_SNP_ID_10260276 A-to-I Human chr1 + 39404623 39404623 39404623 ACGATTTTCTCAGCTCAACCTCCCAAGTAGCTAGGACTACAGATGCACATGCCTGGCCAATTTTT ACGATTTTCTCAGCTCAACCTCCCAAGTAGCTGGGACTACAGATGCACATGCCTGGCCAATTTTT A G MACF1 Ensembl:ENSG00000127603 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1243856436 Functional Loss SNV dbSNP153 33..33 33 - - - 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 31390 RMVar_ID_31390 Human_SNP_ID_10263699 A-to-I Human chr1 + 39415475 39415469 39415476 CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCCGCCACTACGCCCGGCAATTTTTT CTCCTGCCTCAGCCTCCCGAGTAGCTG_______AGGCGCCCGCCACTACGCCCGGCAATTTTTT GGGACTAC G MACF1 Ensembl:ENSG00000127603 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1368729866 Functional Loss DEL dbSNP153 28..34 33 - - - 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 31391 RMVar_ID_31391 Human_SNP_ID_10263700 A-to-I Human chr1 + 39415475 39415475 39415475 CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCCGCCACTACGCCCGGCAATTTTTT CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTGCAGGCGCCCGCCACTACGCCCGGCAATTTTTT A G MACF1 Ensembl:ENSG00000127603 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1464579395 Functional Loss SNV dbSNP153 33..33 33 - - - 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 31392 RMVar_ID_31392 Human_SNP_ID_10263701 A-to-I Human chr1 + 39415477 39415477 39415477 CCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCCGCCACTACGCCCGGCAATTTTTTGT CCTGCCTCAGCCTCCCGAGTAGCTGGGACTACGGGCGCCCGCCACTACGCCCGGCAATTTTTTGT A G MACF1 Ensembl:ENSG00000127603 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1299923877 Functional Loss SNV dbSNP153 33..33 33 - - - 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 31393 RMVar_ID_31393 Human_SNP_ID_10263919 A-to-I Human chr1 + 39416384 39416384 39416384 CAGAATATTTCACACCAGGCACAGTGGCTCACACCTCTAATCCCAACATTTGGGAAGCCAAGGGA CAGAATATTTCACACCAGGCACAGTGGCTCACGCCTCTAATCCCAACATTTGGGAAGCCAAGGGA A G MACF1 Ensembl:ENSG00000127603 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1427494363 Functional Loss SNV dbSNP153 33..33 33 - - - 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 31394 RMVar_ID_31394 Human_SNP_ID_10275364 A-to-I Human chr1 + 39459245 39459245 39459245 AAGGAAACTGAATGATGCCTTGGATCGGCTGGAGGAGGTAATGCCCTGCTGAGTGGCCTTCCCTG AAGGAAACTGAATGATGCCTTGGATCGGCTGGGGGAGGTAATGCCCTGCTGAGTGGCCTTCCCTG A G MACF1 Ensembl:ENSG00000127603 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs761682994 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_96841,Human_RBP_ID_803749,Human_RBP_ID_851454,Human_RBP_ID_8749188,Human_RBP_ID_18968059,Human_RBP_ID_22636798,Human_RBP_ID_22870828,Human_RBP_ID_26314048 Human_Splice_Rec_50001,Human_Splice_Rec_50199,Human_Splice_Rec_50383,Human_Splice_Rec_50715,Human_Splice_Rec_50927,Human_Splice_Rec_51293,Human_Splice_Rec_51423,Human_Splice_Rec_51475,Human_Splice_Rec_51493,Human_Splice_Rec_51499 Human_miRNA_ID_2972064,Human_miRNA_ID_3005247 RMVar_hsa_circ_96358,RMVar_hsa_circ_131901,RMVar_hsa_circ_365402,RMVar_hsa_circ_96246,RMVar_hsa_circ_131928,RMVar_hsa_circ_266362,RMVar_hsa_circ_342077,RMVar_hsa_circ_26390,RMVar_hsa_circ_131947,RMVar_hsa_circ_345730,RMVar_hsa_circ_131949,RMVar_hsa_circ_300611,RMVar_hsa_circ_321086,RMVar_hsa_circ_371541,RMVar_hsa_circ_306498,RMVar_hsa_circ_131948,RMVar_hsa_circ_36727,RMVar_hsa_circ_131946,RMVar_hsa_circ_288567,RMVar_hsa_circ_72309,RMVar_hsa_circ_24314,RMVar_hsa_circ_47065,RMVar_hsa_circ_336690,RMVar_hsa_circ_346179,RMVar_hsa_circ_301746,RMVar_hsa_circ_131951 31395 RMVar_ID_31395 Human_SNP_ID_10293542 A-to-I Human chr1 - 39532900 39532900 39532900 TCCAGGAGTCTGAGACCAGCCCGAGTCAACATAATGAGACCTCATCTCTACAAAAATATATATAA TCCAGGAGTCTGAGACCAGCCCGAGTCAACATGATGAGACCTCATCTCTACAAAAATATATATAA T C PPIEL Ensembl:ENSG00000243970 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs369467384 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5822522,Human_RBP_ID_19355162 RMVar_hsa_circ_131955,RMVar_hsa_circ_7046,RMVar_hsa_circ_43307,RMVar_hsa_circ_272721,RMVar_hsa_circ_308231,RMVar_hsa_circ_346767,RMVar_hsa_circ_72011,RMVar_hsa_circ_131956,RMVar_hsa_circ_131957 31396 RMVar_ID_31396 Human_SNP_ID_10293565 A-to-I Human chr1 - 39532977 39532977 39532977 ACAAAACAGGCCAGGCATGGTGGTTCACACTCATAATCCCAGCACGTTGGGAGACTGAAGTGGGA ACAAAACAGGCCAGGCATGGTGGTTCACACTCGTAATCCCAGCACGTTGGGAGACTGAAGTGGGA T C PPIEL Ensembl:ENSG00000243970 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1200564367 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8241490 RMVar_hsa_circ_131955,RMVar_hsa_circ_7046,RMVar_hsa_circ_43307,RMVar_hsa_circ_272721,RMVar_hsa_circ_308231,RMVar_hsa_circ_346767,RMVar_hsa_circ_72011,RMVar_hsa_circ_131956,RMVar_hsa_circ_131957 31397 RMVar_ID_31397 Human_SNP_ID_10293782 A-to-I Human chr1 - 39533905 39533905 39533905 TTTTTTTAATTGGGATGGGGTCTTGCTATGTTATCTAGGCTGGTCTCGAACTCCAGGGCTCAAGC TTTTTTTAATTGGGATGGGGTCTTGCTATGTTTTCTAGGCTGGTCTCGAACTCCAGGGCTCAAGC T A PPIEL Ensembl:ENSG00000243970 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1284549511 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_131955,RMVar_hsa_circ_7046,RMVar_hsa_circ_43307,RMVar_hsa_circ_272721,RMVar_hsa_circ_308231,RMVar_hsa_circ_346767,RMVar_hsa_circ_72011,RMVar_hsa_circ_131956,RMVar_hsa_circ_131957 31398 RMVar_ID_31398 Human_SNP_ID_10294872 A-to-I Human chr1 - 39537947 39537947 39537947 GTTCGTGCCTGTAATCCCAGCACTTTAGGCTTAGGCAGGCAGATTGCTTGAGCCCTGGAGTTTGA GTTCGTGCCTGTAATCCCAGCACTTTAGGCTTCGGCAGGCAGATTGCTTGAGCCCTGGAGTTTGA T G PPIEL Ensembl:ENSG00000243970 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1284622186 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_131955,RMVar_hsa_circ_7046,RMVar_hsa_circ_43307,RMVar_hsa_circ_272721,RMVar_hsa_circ_308231,RMVar_hsa_circ_346767,RMVar_hsa_circ_72011,RMVar_hsa_circ_131956,RMVar_hsa_circ_131957 31399 RMVar_ID_31399 Human_SNP_ID_10296563 A-to-I Human chr1 - 39545240 39545240 39545240 ACAAAGTTAGACGGGTATAGTGCGATGTGCCTATAGTTCCAGCTATTTGGGAGGCTGAGACAAGA ACAAAGTTAGACGGGTATAGTGCGATGTGCCTGTAGTTCCAGCTATTTGGGAGGCTGAGACAAGA T C PPIEL Ensembl:ENSG00000243970 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053728897 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_131955,RMVar_hsa_circ_43307,RMVar_hsa_circ_308231,RMVar_hsa_circ_346767,RMVar_hsa_circ_72011,RMVar_hsa_circ_131956,RMVar_hsa_circ_66998 31400 RMVar_ID_31400 Human_SNP_ID_10345131 A-to-I Human chr1 + 39739097 39739097 39739097 GCGATAGCTCTGGCTGTGCTTAAACTCCTTCCAAGGTTTCCCACTGTCCTCAGGAAAAAGTGCAG GCGATAGCTCTGGCTGTGCTTAAACTCCTTCCGAGGTTTCCCACTGTCCTCAGGAAAAAGTGCAG A G PPIE Ensembl:ENSG00000084072 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1367815973 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18574706 RMVar_hsa_circ_11590 31401 RMVar_ID_31401 Human_SNP_ID_10345160 A-to-I Human chr1 + 39739195 39739195 39739195 TGCTTTGCTTCCCGATTCGCTGGGTCTCCCGAAAAATGACCCACTTGCCCCCAAGGTTCAGGTTA TGCTTTGCTTCCCGATTCGCTGGGTCTCCCGAGAAATGACCCACTTGCCCCCAAGGTTCAGGTTA A G PPIE Ensembl:ENSG00000084072 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1053368087 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_52251 RMVar_hsa_circ_11590 31402 RMVar_ID_31402 Human_SNP_ID_10348140 A-to-I Human chr1 + 39751560 39751560 39751560 TTTTAAGTTTTTTGTAGAGACAGGGTTTCATTATATTGCTCAGGCTAGTCTGGAACTCTTAGCTT TTTTAAGTTTTTTGTAGAGACAGGGTTTCATTTTATTGCTCAGGCTAGTCTGGAACTCTTAGCTT A T PPIE Ensembl:ENSG00000084072 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs950976129 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70265 31403 RMVar_ID_31403 Human_SNP_ID_10350683 A-to-I Human chr1 + 39762326 39762326 39762326 TGGGCTCGTGTGCTGCGATTACAGGGTGAGCCACCGCACCTGATCAAGGCATCACCGTTGAACCT TGGGCTCGTGTGCTGCGATTACAGGGTGAGCCGCCGCACCTGATCAAGGCATCACCGTTGAACCT A G PPIE Ensembl:ENSG00000084072 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs573967791 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_52264,Human_Splice_Rec_52265 31404 RMVar_ID_31404 Human_SNP_ID_10374006 A-to-I Human chr1 - 39855008 39855008 39855008 CCTTACCTCTACAAAAAATACAAAAATTAGCCAGATGTGGTGGCATGTGCTTGTAGTCCCAGCTA CCTTACCTCTACAAAAAATACAAAAATTAGCCGGATGTGGTGGCATGTGCTTGTAGTCCCAGCTA T C TRIT1 Ensembl:ENSG00000043514 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1442299640 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120389,RMVar_hsa_circ_377449,RMVar_hsa_circ_131971,RMVar_hsa_circ_131974,RMVar_hsa_circ_131975,RMVar_hsa_circ_326611,RMVar_hsa_circ_131976,RMVar_hsa_circ_104330,RMVar_hsa_circ_25192,RMVar_hsa_circ_36919,RMVar_hsa_circ_131977,RMVar_hsa_circ_87369,RMVar_hsa_circ_131978,RMVar_hsa_circ_131985,RMVar_hsa_circ_131980,RMVar_hsa_circ_131979,RMVar_hsa_circ_289012,RMVar_hsa_circ_131981,RMVar_hsa_circ_311725,RMVar_hsa_circ_321660,RMVar_hsa_circ_281554,RMVar_hsa_circ_131983,RMVar_hsa_circ_131984,RMVar_hsa_circ_131982 31405 RMVar_ID_31405 Human_SNP_ID_10374030 A-to-I Human chr1 - 39855134 39855134 39855134 AAAAAAGTTATTTTCGGCCAGGCACGATGGCTATCGCCTGTAACCTCAGCACTTTGGGATGCTGC AAAAAAGTTATTTTCGGCCAGGCACGATGGCTGTCGCCTGTAACCTCAGCACTTTGGGATGCTGC T C TRIT1 Ensembl:ENSG00000043514 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs192315298 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10981195 RMVar_hsa_circ_120389,RMVar_hsa_circ_377449,RMVar_hsa_circ_131971,RMVar_hsa_circ_131974,RMVar_hsa_circ_131975,RMVar_hsa_circ_326611,RMVar_hsa_circ_131976,RMVar_hsa_circ_104330,RMVar_hsa_circ_25192,RMVar_hsa_circ_36919,RMVar_hsa_circ_131977,RMVar_hsa_circ_87369,RMVar_hsa_circ_131978,RMVar_hsa_circ_131985,RMVar_hsa_circ_131980,RMVar_hsa_circ_131979,RMVar_hsa_circ_289012,RMVar_hsa_circ_131981,RMVar_hsa_circ_311725,RMVar_hsa_circ_321660,RMVar_hsa_circ_281554,RMVar_hsa_circ_131983,RMVar_hsa_circ_131984,RMVar_hsa_circ_131982 31406 RMVar_ID_31406 Human_SNP_ID_10374191 A-to-I Human chr1 - 39855918 39855918 39855918 CTGCCTCGGCCTCCCAAAGTGCTGGAATTACAAGTGTGAGCCACCACGCCTGGCCCCAATCAGCC CTGCCTCGGCCTCCCAAAGTGCTGGAATTACACGTGTGAGCCACCACGCCTGGCCCCAATCAGCC T G TRIT1 Ensembl:ENSG00000043514 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs891475445 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120389,RMVar_hsa_circ_377449,RMVar_hsa_circ_131971,RMVar_hsa_circ_131974,RMVar_hsa_circ_131975,RMVar_hsa_circ_326611,RMVar_hsa_circ_131976,RMVar_hsa_circ_104330,RMVar_hsa_circ_25192,RMVar_hsa_circ_36919,RMVar_hsa_circ_131977,RMVar_hsa_circ_87369,RMVar_hsa_circ_131978,RMVar_hsa_circ_131985,RMVar_hsa_circ_131980,RMVar_hsa_circ_131979,RMVar_hsa_circ_289012,RMVar_hsa_circ_131981,RMVar_hsa_circ_311725,RMVar_hsa_circ_321660,RMVar_hsa_circ_281554,RMVar_hsa_circ_131983,RMVar_hsa_circ_131984,RMVar_hsa_circ_131982 31407 RMVar_ID_31407 Human_SNP_ID_10374208 A-to-I Human chr1 - 39856010 39856010 39856010 GAGCCACCATGCCCGGCTATTTTATTTTTTGTAGAGATGGATTTTGCTATGTTGACAAGCTGGTC GAGCCACCATGCCCGGCTATTTTATTTTTTGTGGAGATGGATTTTGCTATGTTGACAAGCTGGTC T C TRIT1 Ensembl:ENSG00000043514 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893008557 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5823169,Human_RBP_ID_10981229 RMVar_hsa_circ_120389,RMVar_hsa_circ_377449,RMVar_hsa_circ_131971,RMVar_hsa_circ_131974,RMVar_hsa_circ_131975,RMVar_hsa_circ_326611,RMVar_hsa_circ_131976,RMVar_hsa_circ_104330,RMVar_hsa_circ_25192,RMVar_hsa_circ_36919,RMVar_hsa_circ_131977,RMVar_hsa_circ_87369,RMVar_hsa_circ_131978,RMVar_hsa_circ_131985,RMVar_hsa_circ_131980,RMVar_hsa_circ_131979,RMVar_hsa_circ_289012,RMVar_hsa_circ_131981,RMVar_hsa_circ_311725,RMVar_hsa_circ_321660,RMVar_hsa_circ_281554,RMVar_hsa_circ_131983,RMVar_hsa_circ_131984,RMVar_hsa_circ_131982 31408 RMVar_ID_31408 Human_SNP_ID_10376234 A-to-I Human chr1 - 39864562 39864562 39864562 ACAGAGTCTCGCTCTGTCAGTGCAGTGGCGCAATCTTGGCTCACTGCAAGCTCCGCCTCCCGGGT ACAGAGTCTCGCTCTGTCAGTGCAGTGGCGCAGTCTTGGCTCACTGCAAGCTCCGCCTCCCGGGT T C TRIT1 Ensembl:ENSG00000043514 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1040244639 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_131982 31409 RMVar_ID_31409 Human_SNP_ID_10376542 A-to-I Human chr1 - 39865767 39865767 39865767 ATGGCCCACTGCAGCTCACCCTCTTGGGCTCAAATGACCCTCCCATCTTAGCCTCCTGAGTAGTT ATGGCCCACTGCAGCTCACCCTCTTGGGCTCAGATGACCCTCCCATCTTAGCCTCCTGAGTAGTT T C TRIT1 Ensembl:ENSG00000043514 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1219092246 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_131982 31410 RMVar_ID_31410 Human_SNP_ID_10376847 A-to-I Human chr1 - 39866870 39866870 39866870 CTCCCACCTCAGTCTCCTGAGCAGCTAGAACTATAGGCACGTGCCACCATGCCTGGCTGATTAAA CTCCCACCTCAGTCTCCTGAGCAGCTAGAACTGTAGGCACGTGCCACCATGCCTGGCTGATTAAA T C TRIT1 Ensembl:ENSG00000043514 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1471761933 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10981648 RMVar_hsa_circ_131982 31411 RMVar_ID_31411 Human_SNP_ID_10421236 A-to-I Human chr1 + 40043706 40043706 40043706 CAAGACCATCCTAGCCAACATGGTGAAACACCATCACTACTAAAAATACAAAAATTAGCTGGGCG CAAGACCATCCTAGCCAACATGGTGAAACACCGTCACTACTAAAAATACAAAAATTAGCTGGGCG A G CAP1 Ensembl:ENSG00000131236 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1233245786 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116220,RMVar_hsa_circ_131994,RMVar_hsa_circ_131993,RMVar_hsa_circ_378856 31412 RMVar_ID_31412 Human_SNP_ID_10422689 A-to-I Human chr1 + 40049445 40049445 40049445 TTTAGCCAGGCTGGTCTCGAACTCTTGACCTCAGGTTATCTACCCGCCTCAGCCTCCCTAAGTGC TTTAGCCAGGCTGGTCTCGAACTCTTGACCTCCGGTTATCTACCCGCCTCAGCCTCCCTAAGTGC A C CAP1 Ensembl:ENSG00000131236 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1400024563 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116220,RMVar_hsa_circ_131994,RMVar_hsa_circ_131993,RMVar_hsa_circ_378856 31413 RMVar_ID_31413 Human_SNP_ID_10423936 A-to-I Human chr1 + 40054320 40054320 40054320 TCAAGCAATTCTCATGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCGCATACCACCACGCCTG TCAAGCAATTCTCATGCCTCAGCCTCCCAAGTCGCTGGGACTACAGGCGCATACCACCACGCCTG A C CAP1 Ensembl:ENSG00000131236 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1365065186 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116220,RMVar_hsa_circ_131994,RMVar_hsa_circ_131993,RMVar_hsa_circ_378856 31414 RMVar_ID_31414 Human_SNP_ID_10429418 A-to-I Human chr1 + 40076490 40076490 40076490 CCGTCTCAAAGAAAAAAAAAGGAATGCCCCTCATCATGCATGGAGGCTTCCTGGATTTGTAGCAG CCGTCTCAAAGAAAAAAAAAGGAATGCCCCTCGTCATGCATGGAGGCTTCCTGGATTTGTAGCAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs960766982 Functional Loss SNV dbSNP153 33..33 33 - - - 31415 RMVar_ID_31415 Human_SNP_ID_10451651 A-to-I Human chr1 + 40168504 40168504 40168504 CTGGCCTCAAGTGATCTGCCCACAGCTTCCCAAAGTGCTGGGATTACAGGCGTGAGCCATTGCAC CTGGCCTCAAGTGATCTGCCCACAGCTTCCCATAGTGCTGGGATTACAGGCGTGAGCCATTGCAC A T RLF Ensembl:ENSG00000117000 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs552210670 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120866,RMVar_hsa_circ_132013 31416 RMVar_ID_31416 Human_SNP_ID_10452194 A-to-I Human chr1 + 40170277 40170277 40170277 CTTTTTTTTGTTTTTTGGTTTTTTTTTGAGACAGGGTCTTGCTGTGTCGCTCAGGCTGGAGTGCG CTTTTTTTTGTTTTTTGGTTTTTTTTTGAGACGGGGTCTTGCTGTGTCGCTCAGGCTGGAGTGCG A G RLF Ensembl:ENSG00000117000 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs373890156 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557821 RMVar_hsa_circ_120866,RMVar_hsa_circ_132013,RMVar_hsa_circ_132015 31417 RMVar_ID_31417 Human_SNP_ID_10452259 A-to-I Human chr1 + 40170470 40170470 40170470 TTTTGTAGAGATAGGGTTTCGCCACGTTGTCCAAGCTGGTTTCAAACTGCTGAGCTCAAGTGAGC TTTTGTAGAGATAGGGTTTCGCCACGTTGTCCGAGCTGGTTTCAAACTGCTGAGCTCAAGTGAGC A G RLF Ensembl:ENSG00000117000 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910148638 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557131 RMVar_hsa_circ_120866,RMVar_hsa_circ_132013,RMVar_hsa_circ_132015 31418 RMVar_ID_31418 Human_SNP_ID_10452406 A-to-I Human chr1 + 40171075 40171075 40171075 TAGAGACAGGATCGTACTCCCTTGCTCAGGCTAGAATGCAGTGGTACAATCTTAGCTTACAGTAA TAGAGACAGGATCGTACTCCCTTGCTCAGGCTGGAATGCAGTGGTACAATCTTAGCTTACAGTAA A G RLF Ensembl:ENSG00000117000 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs997995394 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120866,RMVar_hsa_circ_132013,RMVar_hsa_circ_132015 31419 RMVar_ID_31419 Human_SNP_ID_10452416 A-to-I Human chr1 + 40171120 40171120 40171120 ACAATCTTAGCTTACAGTAACCTCAAACTCTTAGGCTCAAGTGATCCTCCCACCCCAGCCTCTCA ACAATCTTAGCTTACAGTAACCTCAAACTCTTCGGCTCAAGTGATCCTCCCACCCCAGCCTCTCA A C RLF Ensembl:ENSG00000117000 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1438538425 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5823540 RMVar_hsa_circ_120866,RMVar_hsa_circ_132013,RMVar_hsa_circ_132015 31420 RMVar_ID_31420 Human_SNP_ID_10453022 A-to-I Human chr1 + 40173575 40173575 40173575 TTGCTCTGTTGCTTAGGCTGTAGTGCAGTGTTACAATCTCAGCTCACTGCAACCTCTGCTTCCTG TTGCTCTGTTGCTTAGGCTGTAGTGCAGTGTTGCAATCTCAGCTCACTGCAACCTCTGCTTCCTG A G RLF Ensembl:ENSG00000117000 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs556474891 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120866,RMVar_hsa_circ_132013,RMVar_hsa_circ_132015 31421 RMVar_ID_31421 Human_SNP_ID_10453331 A-to-I Human chr1 + 40174998 40174998 40174998 AAGGCGGGAGGATCTCTTGAAGCCAGGAGTTCAAGACCAAGACTGGGCAACGTAGTGAGACCCTG AAGGCGGGAGGATCTCTTGAAGCCAGGAGTTCGAGACCAAGACTGGGCAACGTAGTGAGACCCTG A G RLF Ensembl:ENSG00000117000 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1021171023 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120866,RMVar_hsa_circ_132013,RMVar_hsa_circ_132015 31422 RMVar_ID_31422 Human_SNP_ID_10455914 A-to-I Human chr1 + 40185135 40185135 40185135 ATGGTGATGCACTTCTCCAGTCCTAGCTACTCAGGAGGCTGAGGTGGGTGGGAGAGAGGATCACT ATGGTGATGCACTTCTCCAGTCCTAGCTACTCTGGAGGCTGAGGTGGGTGGGAGAGAGGATCACT A T RLF Ensembl:ENSG00000117000 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1353315635 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120866,RMVar_hsa_circ_132013,RMVar_hsa_circ_132015 31423 RMVar_ID_31423 Human_SNP_ID_10461237 A-to-I Human chr1 + 40205268 40205268 40205268 TTGAGCCCGGGAATTGCTTGAGCCCAGGAGGCAGAGGCTGCAGTAAGCTGAGATCACGCCACTGC TTGAGCCCGGGAATTGCTTGAGCCCAGGAGGCGGAGGCTGCAGTAAGCTGAGATCACGCCACTGC A G RLF Ensembl:ENSG00000117000 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs369886110 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23303531 RMVar_hsa_circ_105128,RMVar_hsa_circ_373346,RMVar_hsa_circ_286427,RMVar_hsa_circ_132019,RMVar_hsa_circ_132020,RMVar_hsa_circ_331844,RMVar_hsa_circ_377205,RMVar_hsa_circ_296700,RMVar_hsa_circ_132021,RMVar_hsa_circ_27686,RMVar_hsa_circ_361667,RMVar_hsa_circ_132024,RMVar_hsa_circ_132026 31424 RMVar_ID_31424 Human_SNP_ID_10461240 A-to-I Human chr1 + 40205291 40205291 40205291 CCAGGAGGCAGAGGCTGCAGTAAGCTGAGATCACGCCACTGCACTCCAGCCTGGGCAACAGAACA CCAGGAGGCAGAGGCTGCAGTAAGCTGAGATCGCGCCACTGCACTCCAGCCTGGGCAACAGAACA A G RLF Ensembl:ENSG00000117000 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474687788 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105128,RMVar_hsa_circ_373346,RMVar_hsa_circ_286427,RMVar_hsa_circ_132019,RMVar_hsa_circ_132020,RMVar_hsa_circ_331844,RMVar_hsa_circ_377205,RMVar_hsa_circ_296700,RMVar_hsa_circ_132021,RMVar_hsa_circ_27686,RMVar_hsa_circ_361667,RMVar_hsa_circ_132024,RMVar_hsa_circ_132026 31425 RMVar_ID_31425 Human_SNP_ID_10461822 A-to-I Human chr1 + 40207728 40207728 40207728 CACCTCCTGAGTTCAAGCAGTTTTCCTGCCTCAACCACCTGAGTAGCTGGGATTGCAGACGTGCG CACCTCCTGAGTTCAAGCAGTTTTCCTGCCTCGACCACCTGAGTAGCTGGGATTGCAGACGTGCG A G RLF Ensembl:ENSG00000117000 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs571834027 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105128,RMVar_hsa_circ_373346,RMVar_hsa_circ_286427,RMVar_hsa_circ_132019,RMVar_hsa_circ_132020,RMVar_hsa_circ_331844,RMVar_hsa_circ_377205,RMVar_hsa_circ_296700,RMVar_hsa_circ_132021,RMVar_hsa_circ_27686,RMVar_hsa_circ_361667,RMVar_hsa_circ_132024,RMVar_hsa_circ_132026 31426 RMVar_ID_31426 Human_SNP_ID_10465772 A-to-I Human chr1 + 40224460 40224460 40224460 TGCCACGCCCGACTAATTTTTGTATTTTTGGTAGAGACTGGGTTTCACCATGTTGGTCAGGCTGG TGCCACGCCCGACTAATTTTTGTATTTTTGGTGGAGACTGGGTTTCACCATGTTGGTCAGGCTGG A G RLF Ensembl:ENSG00000117000 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1436100453 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105128,RMVar_hsa_circ_373346,RMVar_hsa_circ_132020,RMVar_hsa_circ_377205,RMVar_hsa_circ_296700,RMVar_hsa_circ_132021,RMVar_hsa_circ_361667,RMVar_hsa_circ_132024,RMVar_hsa_circ_132026,RMVar_hsa_circ_278151 31427 RMVar_ID_31427 Human_SNP_ID_10465776 A-to-I Human chr1 + 40224474 40224474 40224474 AATTTTTGTATTTTTGGTAGAGACTGGGTTTCACCATGTTGGTCAGGCTGGTCTCAAACTCCTGA AATTTTTGTATTTTTGGTAGAGACTGGGTTTCGCCATGTTGGTCAGGCTGGTCTCAAACTCCTGA A G RLF Ensembl:ENSG00000117000 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs796245588 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105128,RMVar_hsa_circ_373346,RMVar_hsa_circ_132020,RMVar_hsa_circ_377205,RMVar_hsa_circ_296700,RMVar_hsa_circ_132021,RMVar_hsa_circ_361667,RMVar_hsa_circ_132024,RMVar_hsa_circ_132026,RMVar_hsa_circ_278151 31428 RMVar_ID_31428 Human_SNP_ID_10465789 A-to-I Human chr1 + 40224534 40224533 40224534 CCTGACCTTGTGATCCACTGCCTCAGCCTCCCAAAGTGCTAGGGTTACAGACGTGAGCCACTGCG CCTGACCTTGTGATCCACTGCCTCAGCCTCCC_AAGTGCTAGGGTTACAGACGTGAGCCACTGCG CA C RLF Ensembl:ENSG00000117000 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs200229123 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_24696782 RMVar_hsa_circ_105128,RMVar_hsa_circ_373346,RMVar_hsa_circ_132020,RMVar_hsa_circ_377205,RMVar_hsa_circ_296700,RMVar_hsa_circ_132021,RMVar_hsa_circ_361667,RMVar_hsa_circ_132024,RMVar_hsa_circ_132026,RMVar_hsa_circ_278151 31429 RMVar_ID_31429 Human_SNP_ID_10465790 A-to-I Human chr1 + 40224534 40224534 40224534 CCTGACCTTGTGATCCACTGCCTCAGCCTCCCAAAGTGCTAGGGTTACAGACGTGAGCCACTGCG CCTGACCTTGTGATCCACTGCCTCAGCCTCCCCAAGTGCTAGGGTTACAGACGTGAGCCACTGCG A C RLF Ensembl:ENSG00000117000 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1557757365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24696782 RMVar_hsa_circ_105128,RMVar_hsa_circ_373346,RMVar_hsa_circ_132020,RMVar_hsa_circ_377205,RMVar_hsa_circ_296700,RMVar_hsa_circ_132021,RMVar_hsa_circ_361667,RMVar_hsa_circ_132024,RMVar_hsa_circ_132026,RMVar_hsa_circ_278151 31430 RMVar_ID_31430 Human_SNP_ID_10465791 A-to-I Human chr1 + 40224535 40224535 40224535 CTGACCTTGTGATCCACTGCCTCAGCCTCCCAAAGTGCTAGGGTTACAGACGTGAGCCACTGCGC CTGACCTTGTGATCCACTGCCTCAGCCTCCCACAGTGCTAGGGTTACAGACGTGAGCCACTGCGC A C RLF Ensembl:ENSG00000117000 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1280584264 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24696782 RMVar_hsa_circ_105128,RMVar_hsa_circ_373346,RMVar_hsa_circ_132020,RMVar_hsa_circ_377205,RMVar_hsa_circ_296700,RMVar_hsa_circ_132021,RMVar_hsa_circ_361667,RMVar_hsa_circ_132024,RMVar_hsa_circ_132026,RMVar_hsa_circ_278151 31431 RMVar_ID_31431 Human_SNP_ID_10466337 A-to-I Human chr1 + 40225931 40225931 40225931 AAAAAAGCCGGATGGTAGTGGTACGCACCTATAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA AAAAAAGCCGGATGGTAGTGGTACGCACCTATGATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA A G RLF Ensembl:ENSG00000117000 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1373109643 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105128,RMVar_hsa_circ_373346,RMVar_hsa_circ_132020,RMVar_hsa_circ_377205,RMVar_hsa_circ_296700,RMVar_hsa_circ_132021,RMVar_hsa_circ_361667,RMVar_hsa_circ_132024,RMVar_hsa_circ_132026,RMVar_hsa_circ_278151 31432 RMVar_ID_31432 Human_SNP_ID_10466787 A-to-I Human chr1 + 40227947 40227947 40227947 ATCGCTTGAACCTGGGTGGCAGAGGTTGCAGTAAGCCGATATCGCACCACTGCACTCCAGCCTGA ATCGCTTGAACCTGGGTGGCAGAGGTTGCAGTGAGCCGATATCGCACCACTGCACTCCAGCCTGA A G RLF Ensembl:ENSG00000117000 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1327701169 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22563006 RMVar_hsa_circ_105128,RMVar_hsa_circ_373346,RMVar_hsa_circ_132020,RMVar_hsa_circ_377205,RMVar_hsa_circ_296700,RMVar_hsa_circ_132021,RMVar_hsa_circ_361667,RMVar_hsa_circ_132024,RMVar_hsa_circ_132026,RMVar_hsa_circ_278151 31433 RMVar_ID_31433 Human_SNP_ID_10467291 A-to-I Human chr1 + 40229713 40229713 40229713 CTGACCTTGTGATCCACCTGCCTTGGCCTCCCAAAGTGCTGTGATTACAGCCATGAGACACCACG CTGACCTTGTGATCCACCTGCCTTGGCCTCCCGAAGTGCTGTGATTACAGCCATGAGACACCACG A G RLF Ensembl:ENSG00000117000 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1273544665 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23149595 RMVar_hsa_circ_105128,RMVar_hsa_circ_373346,RMVar_hsa_circ_132020,RMVar_hsa_circ_377205,RMVar_hsa_circ_296700,RMVar_hsa_circ_132021,RMVar_hsa_circ_361667,RMVar_hsa_circ_132024,RMVar_hsa_circ_132026,RMVar_hsa_circ_278151 31434 RMVar_ID_31434 Human_SNP_ID_10467521 A-to-I Human chr1 + 40230605 40230605 40230605 CAGGCATCCACCACCACACTCAGCTAAGTTTTATATTTGTAGTAGAGATGAGGTTTCACCATGTT CAGGCATCCACCACCACACTCAGCTAAGTTTTGTATTTGTAGTAGAGATGAGGTTTCACCATGTT A G RLF Ensembl:ENSG00000117000 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs986941079 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105128,RMVar_hsa_circ_373346,RMVar_hsa_circ_132020,RMVar_hsa_circ_377205,RMVar_hsa_circ_296700,RMVar_hsa_circ_132021,RMVar_hsa_circ_361667,RMVar_hsa_circ_132024,RMVar_hsa_circ_132026,RMVar_hsa_circ_278151 31435 RMVar_ID_31435 Human_SNP_ID_10467537 A-to-I Human chr1 + 40230701 40230701 40230701 GTGATCTGCCCCCCTTCACCTCCCAAAATGCTAGGATTACAGGCATGAGCCACCCGCCATGCCCG GTGATCTGCCCCCCTTCACCTCCCAAAATGCTGGGATTACAGGCATGAGCCACCCGCCATGCCCG A G RLF Ensembl:ENSG00000117000 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1264634351 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105128,RMVar_hsa_circ_373346,RMVar_hsa_circ_132020,RMVar_hsa_circ_377205,RMVar_hsa_circ_296700,RMVar_hsa_circ_132021,RMVar_hsa_circ_361667,RMVar_hsa_circ_132024,RMVar_hsa_circ_132026,RMVar_hsa_circ_278151 31436 RMVar_ID_31436 Human_SNP_ID_10470198 A-to-I Human chr1 + 40241117 40241117 40241117 GAGTTTCGTTCTTGTTGCCCAAGCTGGAGTGCAATGGTGCAGTCTCGACTCACTGCAACCTCCTC GAGTTTCGTTCTTGTTGCCCAAGCTGGAGTGCCATGGTGCAGTCTCGACTCACTGCAACCTCCTC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1284618137 Functional Loss SNV dbSNP153 33..33 33 - - - 31437 RMVar_ID_31437 Human_SNP_ID_10470199 A-to-I Human chr1 + 40241117 40241117 40241117 GAGTTTCGTTCTTGTTGCCCAAGCTGGAGTGCAATGGTGCAGTCTCGACTCACTGCAACCTCCTC GAGTTTCGTTCTTGTTGCCCAAGCTGGAGTGCGATGGTGCAGTCTCGACTCACTGCAACCTCCTC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1284618137 Functional Loss SNV dbSNP153 33..33 33 - - - 31438 RMVar_ID_31438 Human_SNP_ID_10476142 A-to-I Human chr1 + 40264227 40264227 40264227 GTGTTGGCACATGCCTGTAGTCGCAGCTACTCAGGAGGCTGAGACACAAGAATTGCTTGAACCCG GTGTTGGCACATGCCTGTAGTCGCAGCTACTCGGGAGGCTGAGACACAAGAATTGCTTGAACCCG A G ZMPSTE24 Ensembl:ENSG00000084073 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202045411 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_132029,RMVar_hsa_circ_121001,RMVar_hsa_circ_308747,RMVar_hsa_circ_132028,RMVar_hsa_circ_293272 31439 RMVar_ID_31439 Human_SNP_ID_10476266 A-to-I Human chr1 + 40264769 40264769 40264769 GAGTGTGGTGATGTGCACCTGCAGTTCTAGCTACTTGGAGGCTGAGGTGGGAGGGTTGCTGGAGC GAGTGTGGTGATGTGCACCTGCAGTTCTAGCTCCTTGGAGGCTGAGGTGGGAGGGTTGCTGGAGC A C ZMPSTE24 Ensembl:ENSG00000084073 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1389811248 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17751116 RMVar_hsa_circ_132029,RMVar_hsa_circ_121001,RMVar_hsa_circ_308747,RMVar_hsa_circ_132028,RMVar_hsa_circ_293272 31440 RMVar_ID_31440 Human_SNP_ID_10480686 A-to-I Human chr1 + 40282581 40282581 40282581 TTCCAGGCTGGTCGAACTGCTGGCCTCAAGTTACCCGCCTGCCTTGGCCTCCCAAAGTGCTGGGA TTCCAGGCTGGTCGAACTGCTGGCCTCAAGTTGCCCGCCTGCCTTGGCCTCCCAAAGTGCTGGGA A G ZMPSTE24 Ensembl:ENSG00000084073 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1484660971 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121001,RMVar_hsa_circ_132028,RMVar_hsa_circ_4668,RMVar_hsa_circ_317735,RMVar_hsa_circ_84550,RMVar_hsa_circ_132032,RMVar_hsa_circ_132033,RMVar_hsa_circ_323322,RMVar_hsa_circ_354913,RMVar_hsa_circ_132034 31441 RMVar_ID_31441 Human_SNP_ID_10480852 A-to-I Human chr1 + 40283270 40283270 40283270 CCATACCTGTAATCCCAGCACTTTGGAAGGCCAAGACAGGCAGATAACTTGAGGCCAGGAGTTCG CCATACCTGTAATCCCAGCACTTTGGAAGGCCGAGACAGGCAGATAACTTGAGGCCAGGAGTTCG A G ZMPSTE24 Ensembl:ENSG00000084073 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1026917669 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121001,RMVar_hsa_circ_132028,RMVar_hsa_circ_4668,RMVar_hsa_circ_317735,RMVar_hsa_circ_84550,RMVar_hsa_circ_132032,RMVar_hsa_circ_132033,RMVar_hsa_circ_323322,RMVar_hsa_circ_354913,RMVar_hsa_circ_132034 31442 RMVar_ID_31442 Human_SNP_ID_10482693 A-to-I Human chr1 + 40290664 40290664 40290664 TTCTGCATTTTTAGTAGAGACGGGGTTTCACCATGTTAGCCAGGATGGTCTCAATCTCCTGACCT TTCTGCATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGGTCTCAATCTCCTGACCT A G ZMPSTE24 Ensembl:ENSG00000084073 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs191988803 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121001,RMVar_hsa_circ_132028,RMVar_hsa_circ_4668,RMVar_hsa_circ_84550,RMVar_hsa_circ_132033,RMVar_hsa_circ_354913 31443 RMVar_ID_31443 Human_SNP_ID_10482694 A-to-I Human chr1 + 40290669 40290669 40290669 CATTTTTAGTAGAGACGGGGTTTCACCATGTTAGCCAGGATGGTCTCAATCTCCTGACCTCGTGA CATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGATGGTCTCAATCTCCTGACCTCGTGA A G ZMPSTE24 Ensembl:ENSG00000084073 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1048033288 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121001,RMVar_hsa_circ_132028,RMVar_hsa_circ_4668,RMVar_hsa_circ_84550,RMVar_hsa_circ_132033,RMVar_hsa_circ_354913 31444 RMVar_ID_31444 Human_SNP_ID_10509413 A-to-I Human chr1 + 40398329 40398329 40398329 TAGCTCATTGCAGCCTTTGAATCCTTGGGCTCAAGCAGTACTCCCGCTCAGCCTCCCAAGTAGCT TAGCTCATTGCAGCCTTTGAATCCTTGGGCTCCAGCAGTACTCCCGCTCAGCCTCCCAAGTAGCT A C SMAP2 Ensembl:ENSG00000084070 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs187622925 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_132037 31445 RMVar_ID_31445 Human_SNP_ID_10510131 A-to-I Human chr1 + 40401142 40401142 40401142 AAAATTAGCCGGGCGTGATCGCGGGCGCCTGTAGTCTCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTAGCCGGGCGTGATCGCGGGCGCCTGTGGTCTCAGCTACTCGGGAGGCTGAGGCAGGAGA A G SMAP2 Ensembl:ENSG00000084070 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928071056 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_132037 31446 RMVar_ID_31446 Human_SNP_ID_10522449 A-to-I Human chr1 + 40455729 40455729 40455729 TGCTGCACCCATCAACCCGTCATCTACATTAGATATTTCTCCTAATGCTATCCCTCCCCTAGCCC TGCTGCACCCATCAACCCGTCATCTACATTAGGTATTTCTCCTAATGCTATCCCTCCCCTAGCCC A G ZFP69B Ensembl:ENSG00000187801 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1308246519 Functional Loss SNV dbSNP153 33..33 33 - - - 31447 RMVar_ID_31447 Human_SNP_ID_10541569 A-to-I Human chr1 + 40534872 40534872 40534872 TTAATTAGCATGGCATGATGGCACACACCTGTAGTTCCAGCTACTAGGTAGGCTAGGGCAGGAGG TTAATTAGCATGGCATGATGGCACACACCTGTCGTTCCAGCTACTAGGTAGGCTAGGGCAGGAGG A C ZNF684 Ensembl:ENSG00000117010 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947855982 Functional Loss SNV dbSNP153 33..33 33 - - - 31448 RMVar_ID_31448 Human_SNP_ID_10541572 A-to-I Human chr1 + 40534885 40534885 40534885 CATGATGGCACACACCTGTAGTTCCAGCTACTAGGTAGGCTAGGGCAGGAGGATCTGTTGAGCCT CATGATGGCACACACCTGTAGTTCCAGCTACTTGGTAGGCTAGGGCAGGAGGATCTGTTGAGCCT A T ZNF684 Ensembl:ENSG00000117010 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971936376 Functional Loss SNV dbSNP153 33..33 33 - - - 31449 RMVar_ID_31449 Human_SNP_ID_10541587 A-to-I Human chr1 + 40534942 40534942 40534942 TTGAGCCTAGAAGATCAAGGCTATAGCTAGCTATGGTCACAGCACTGCACTCTAGCCTGGGTGAC TTGAGCCTAGAAGATCAAGGCTATAGCTAGCTCTGGTCACAGCACTGCACTCTAGCCTGGGTGAC A C ZNF684 Ensembl:ENSG00000117010 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs140749199 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10985081 31450 RMVar_ID_31450 Human_SNP_ID_10541588 A-to-I Human chr1 + 40534942 40534942 40534942 TTGAGCCTAGAAGATCAAGGCTATAGCTAGCTATGGTCACAGCACTGCACTCTAGCCTGGGTGAC TTGAGCCTAGAAGATCAAGGCTATAGCTAGCTGTGGTCACAGCACTGCACTCTAGCCTGGGTGAC A G ZNF684 Ensembl:ENSG00000117010 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs140749199 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10985081 31451 RMVar_ID_31451 Human_SNP_ID_10581624 A-to-I Human chr1 + 40698526 40698526 40698526 TCGGCTCACTGCAACCTCTGCCTTTTGGGTTCAGACGATTCTCCTGCCTCAGCCTCCTGAGTAGC TCGGCTCACTGCAACCTCTGCCTTTTGGGTTCGGACGATTCTCCTGCCTCAGCCTCCTGAGTAGC A G NFYC Ensembl:ENSG00000066136 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1330000201 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100713,RMVar_hsa_circ_98356,RMVar_hsa_circ_132057,RMVar_hsa_circ_132058 31452 RMVar_ID_31452 Human_SNP_ID_10581718 A-to-I Human chr1 + 40698909 40698909 40698909 GAGATGGGCCGGGCGCCGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGCAG GAGATGGGCCGGGCGCCGTGGCTCACACCTGTCATCCCAGCACTTTGGGAGGCTGAGGCGGGCAG A C NFYC Ensembl:ENSG00000066136 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1482498840 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100713,RMVar_hsa_circ_98356,RMVar_hsa_circ_132057,RMVar_hsa_circ_132058 31453 RMVar_ID_31453 Human_SNP_ID_10587173 A-to-I Human chr1 + 40721619 40721619 40721619 GGTCTCACTCTGTTGCCAGGCTGAAGTGCAGTAGTGCAATCATGGCTCATTGCAGTCTCCCAGCT GGTCTCACTCTGTTGCCAGGCTGAAGTGCAGTGGTGCAATCATGGCTCATTGCAGTCTCCCAGCT A G NFYC Ensembl:ENSG00000066136 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1475084216 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_53892,Human_Splice_Rec_53893 RMVar_hsa_circ_100713,RMVar_hsa_circ_98356,RMVar_hsa_circ_132057,RMVar_hsa_circ_77376,RMVar_hsa_circ_132058,RMVar_hsa_circ_132059 31454 RMVar_ID_31454 Human_SNP_ID_10590276 A-to-I Human chr1 + 40733805 40733805 40733805 TCGCTCTGTCGCCCAGGCTGTTGTGCAGTGGCATTATCTTGACTCACTGCAACCTCCGCTTCCCA TCGCTCTGTCGCCCAGGCTGTTGTGCAGTGGCGTTATCTTGACTCACTGCAACCTCCGCTTCCCA A G NFYC Ensembl:ENSG00000066136 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1436273821 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18574966 RMVar_hsa_circ_33393,RMVar_hsa_circ_100713,RMVar_hsa_circ_98356,RMVar_hsa_circ_132057,RMVar_hsa_circ_74229,RMVar_hsa_circ_132058,RMVar_hsa_circ_120113,RMVar_hsa_circ_36245,RMVar_hsa_circ_21907,RMVar_hsa_circ_28075,RMVar_hsa_circ_132060 31455 RMVar_ID_31455 Human_SNP_ID_10655763 A-to-I Human chr1 + 40994974 40994974 40994974 GTGAATTCCACTGTTAAATTTCCTAACACAGTAGTTCTCAAACTTGACTGCACACTGGAATCACT GTGAATTCCACTGTTAAATTTCCTAACACAGTGGTTCTCAAACTTGACTGCACACTGGAATCACT A G CTPS1 Ensembl:ENSG00000171793 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs748612847 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10986842 RMVar_hsa_circ_6131,RMVar_hsa_circ_84087,RMVar_hsa_circ_132071,RMVar_hsa_circ_357257,RMVar_hsa_circ_12488,RMVar_hsa_circ_84827,RMVar_hsa_circ_43850,RMVar_hsa_circ_101000,RMVar_hsa_circ_132072,RMVar_hsa_circ_132073,RMVar_hsa_circ_104219,RMVar_hsa_circ_372767,RMVar_hsa_circ_106970,RMVar_hsa_circ_132075,RMVar_hsa_circ_14499,RMVar_hsa_circ_132074,RMVar_hsa_circ_105072,RMVar_hsa_circ_132079,RMVar_hsa_circ_132077,RMVar_hsa_circ_132078,RMVar_hsa_circ_369772 31456 RMVar_ID_31456 Human_SNP_ID_10664238 A-to-I Human chr1 + 41027024 41027024 41027024 TGGGGTTTCACCATGTTGCCCAGGCTGGTCTCAAACTCCTGAGCTCAAGAGATCCTCCCACCTTG TGGGGTTTCACCATGTTGCCCAGGCTGGTCTCTAACTCCTGAGCTCAAGAGATCCTCCCACCTTG A T SLFNL1-AS1 Ensembl:ENSG00000281207 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1305540524 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_348 31457 RMVar_ID_31457 Human_SNP_ID_10667244 A-to-I Human chr1 - 41039705 41039705 41039705 CTTTGGGAGACCGAGGTGGGCAGATCACTTGAAGCCAGGAGTTCAAGACTAGCCTGGCCAACATG CTTTGGGAGACCGAGGTGGGCAGATCACTTGATGCCAGGAGTTCAAGACTAGCCTGGCCAACATG T A SCMH1 Ensembl:ENSG00000010803 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1383322754 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557136 RMVar_hsa_circ_44276,RMVar_hsa_circ_132094,RMVar_hsa_circ_78544,RMVar_hsa_circ_49571,RMVar_hsa_circ_343898,RMVar_hsa_circ_42362,RMVar_hsa_circ_312271,RMVar_hsa_circ_330675,RMVar_hsa_circ_265912,RMVar_hsa_circ_132096 31458 RMVar_ID_31458 Human_SNP_ID_10674668 A-to-I Human chr1 - 41071914 41071914 41071914 CCTGCCTATAATCCCAACACTTTGGGAGGCCAAGGTAGGAGGATCGCTTGAGCAGGAGAAGTTCG CCTGCCTATAATCCCAACACTTTGGGAGGCCAGGGTAGGAGGATCGCTTGAGCAGGAGAAGTTCG T C SCMH1 Ensembl:ENSG00000010803 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs577917525 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49571,RMVar_hsa_circ_343898,RMVar_hsa_circ_300818,RMVar_hsa_circ_312271,RMVar_hsa_circ_330675,RMVar_hsa_circ_265912,RMVar_hsa_circ_132096,RMVar_hsa_circ_328969,RMVar_hsa_circ_123364,RMVar_hsa_circ_28244,RMVar_hsa_circ_308360,RMVar_hsa_circ_70096,RMVar_hsa_circ_132097,RMVar_hsa_circ_132098,RMVar_hsa_circ_109672,RMVar_hsa_circ_349450,RMVar_hsa_circ_132100,RMVar_hsa_circ_349711,RMVar_hsa_circ_358992,RMVar_hsa_circ_310553,RMVar_hsa_circ_3541,RMVar_hsa_circ_287483,RMVar_hsa_circ_298905,RMVar_hsa_circ_277541,RMVar_hsa_circ_132103,RMVar_hsa_circ_132104,RMVar_hsa_circ_132102 31459 RMVar_ID_31459 Human_SNP_ID_10676418 A-to-I Human chr1 - 41080061 41080061 41080061 TTTAAAAATCATAATTAAAATGTTAAAATGTAAAAAAGATGAACAAAGTGTAAGAAAAAATAGTA TTTAAAAATCATAATTAAAATGTTAAAATGTAGAAAAGATGAACAAAGTGTAAGAAAAAATAGTA T C SCMH1 Ensembl:ENSG00000010803 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs188395489 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37884,RMVar_hsa_circ_330675,RMVar_hsa_circ_265912,RMVar_hsa_circ_328969,RMVar_hsa_circ_123364,RMVar_hsa_circ_28244,RMVar_hsa_circ_308360,RMVar_hsa_circ_70096,RMVar_hsa_circ_132097,RMVar_hsa_circ_109672,RMVar_hsa_circ_132100,RMVar_hsa_circ_349711,RMVar_hsa_circ_358992,RMVar_hsa_circ_310553,RMVar_hsa_circ_3541,RMVar_hsa_circ_287483,RMVar_hsa_circ_298905,RMVar_hsa_circ_132103,RMVar_hsa_circ_132104,RMVar_hsa_circ_28174 31460 RMVar_ID_31460 Human_SNP_ID_10676419 A-to-I Human chr1 - 41080069 41080062 41080070 ACAGATTTTTTAAAAATCATAATTAAAATGTTAAAATGTAAAAAAGATGAACAAAGTGTAAGAAA ACAGATTTTTTAAAAATCATAATTAAAATGT________AAAAAAGATGAACAAAGTGTAAGAAA TACATTTTA T SCMH1 Ensembl:ENSG00000010803 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1273837228 Functional Loss DEL dbSNP153 32..39 33 - - - RMVar_hsa_circ_37884,RMVar_hsa_circ_330675,RMVar_hsa_circ_265912,RMVar_hsa_circ_328969,RMVar_hsa_circ_123364,RMVar_hsa_circ_28244,RMVar_hsa_circ_308360,RMVar_hsa_circ_70096,RMVar_hsa_circ_132097,RMVar_hsa_circ_109672,RMVar_hsa_circ_132100,RMVar_hsa_circ_349711,RMVar_hsa_circ_358992,RMVar_hsa_circ_310553,RMVar_hsa_circ_3541,RMVar_hsa_circ_287483,RMVar_hsa_circ_298905,RMVar_hsa_circ_132103,RMVar_hsa_circ_132104,RMVar_hsa_circ_28174 31461 RMVar_ID_31461 Human_SNP_ID_10695819 A-to-I Human chr1 - 41166126 41166125 41166126 ATGCATCTACAGTCAATTGCTTTTTGACAGGAACACACATTGAGGAAAGGACAATCTGTTCAAAA ATGCATCTACAGTCAATTGCTTTTTGACAGGA_CACACATTGAGGAAAGGACAATCTGTTCAAAA GT G SCMH1 Ensembl:ENSG00000010803 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1441872261 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_22520258,Human_RBP_ID_26314069,Human_RBP_ID_26767661 RMVar_hsa_circ_349711,RMVar_hsa_circ_300783,RMVar_hsa_circ_83050,RMVar_hsa_circ_132109,RMVar_hsa_circ_132108,RMVar_hsa_circ_321528,RMVar_hsa_circ_16933,RMVar_hsa_circ_50117,RMVar_hsa_circ_277592 31462 RMVar_ID_31462 Human_SNP_ID_10695820 A-to-I Human chr1 - 41166132 41166132 41166132 AAACCCATGCATCTACAGTCAATTGCTTTTTGACAGGAACACACATTGAGGAAAGGACAATCTGT AAACCCATGCATCTACAGTCAATTGCTTTTTGTCAGGAACACACATTGAGGAAAGGACAATCTGT T A SCMH1 Ensembl:ENSG00000010803 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1373524466 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22520258,Human_RBP_ID_26314069,Human_RBP_ID_26767661 RMVar_hsa_circ_349711,RMVar_hsa_circ_300783,RMVar_hsa_circ_83050,RMVar_hsa_circ_132109,RMVar_hsa_circ_132108,RMVar_hsa_circ_321528,RMVar_hsa_circ_16933,RMVar_hsa_circ_50117,RMVar_hsa_circ_277592 31463 RMVar_ID_31463 Human_SNP_ID_10935325 A-to-I Human chr1 - 42183237 42183237 42183237 CTCTCTCTTCTCTTTTGACAGGGTCTCACTCTATTAACCAGGCTGGAGTGTAGTAGCACAATCTC CTCTCTCTTCTCTTTTGACAGGGTCTCACTCTGTTAACCAGGCTGGAGTGTAGTAGCACAATCTC T C FOXJ3 Ensembl:ENSG00000198815 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1479822152 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_355548,Human_RBP_ID_8311547,Human_RBP_ID_18929621,Human_RBP_ID_24698729 RMVar_hsa_circ_12576,RMVar_hsa_circ_266183 31464 RMVar_ID_31464 Human_SNP_ID_11004075 A-to-I Human chr1 + 42459337 42459337 42459337 GGTGGGTGCCACCATGCTTGGCTAATTTTTGTATTTTTTTGTAGAGACATGGTTTTGCCATGTTG GGTGGGTGCCACCATGCTTGGCTAATTTTTGTGTTTTTTTGTAGAGACATGGTTTTGCCATGTTG A G PPCS Ensembl:ENSG00000127125 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1340219817 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_132158,RMVar_hsa_circ_94350 31465 RMVar_ID_31465 Human_SNP_ID_11050989 A-to-I Human chr1 + 42670961 42670961 42670961 GGGATTACAGGCGCACGCTGCCATGCCTGGCTATTTTTTGTATTTTTAGTAGAGACGGGGTTTCA GGGATTACAGGCGCACGCTGCCATGCCTGGCTGTTTTTTGTATTTTTAGTAGAGACGGGGTTTCA A G PPIH Ensembl:ENSG00000171960 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs919801345 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10993065 RMVar_hsa_circ_102044,RMVar_hsa_circ_132175,RMVar_hsa_circ_88700,RMVar_hsa_circ_101370,RMVar_hsa_circ_132176,RMVar_hsa_circ_132178,RMVar_hsa_circ_83543,RMVar_hsa_circ_132180,RMVar_hsa_circ_121465,RMVar_hsa_circ_117381,RMVar_hsa_circ_132182,RMVar_hsa_circ_132183 31466 RMVar_ID_31466 Human_SNP_ID_11051043 A-to-I Human chr1 + 42671200 42671200 42671200 CCTGTAATCCCAGCACTTTGGGAGGCCGAAGCAGGTGGATCGCTTGAGGCCAGGAGTTTGAGACC CCTGTAATCCCAGCACTTTGGGAGGCCGAAGCTGGTGGATCGCTTGAGGCCAGGAGTTTGAGACC A T PPIH Ensembl:ENSG00000171960 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1021592392 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102044,RMVar_hsa_circ_132175,RMVar_hsa_circ_88700,RMVar_hsa_circ_101370,RMVar_hsa_circ_132176,RMVar_hsa_circ_132178,RMVar_hsa_circ_83543,RMVar_hsa_circ_132180,RMVar_hsa_circ_121465,RMVar_hsa_circ_117381,RMVar_hsa_circ_132182,RMVar_hsa_circ_132183 31467 RMVar_ID_31467 Human_SNP_ID_11051057 A-to-I Human chr1 + 42671250 42671250 42671250 CAGGAGTTTGAGACCAGCCTTGCCGACATGGTAAAACCCATCTCTACTAAAATTACAAAAATTAG CAGGAGTTTGAGACCAGCCTTGCCGACATGGTGAAACCCATCTCTACTAAAATTACAAAAATTAG A G PPIH Ensembl:ENSG00000171960 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1198102 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8311657 RMVar_hsa_circ_102044,RMVar_hsa_circ_132175,RMVar_hsa_circ_88700,RMVar_hsa_circ_101370,RMVar_hsa_circ_132176,RMVar_hsa_circ_132178,RMVar_hsa_circ_83543,RMVar_hsa_circ_132180,RMVar_hsa_circ_121465,RMVar_hsa_circ_117381,RMVar_hsa_circ_132182,RMVar_hsa_circ_132183 31468 RMVar_ID_31468 Human_SNP_ID_11051436 A-to-I Human chr1 + 42672923 42672923 42672923 TGCCCGCCTTGACTTCCCAAAGTACTGGGATTACAGGCGTGAGCCACCATGCCTGGTCTGTACAA TGCCCGCCTTGACTTCCCAAAGTACTGGGATTGCAGGCGTGAGCCACCATGCCTGGTCTGTACAA A G PPIH Ensembl:ENSG00000171960 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs948782853 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2148260 RMVar_hsa_circ_102044,RMVar_hsa_circ_132175,RMVar_hsa_circ_88700,RMVar_hsa_circ_101370,RMVar_hsa_circ_132176,RMVar_hsa_circ_132178,RMVar_hsa_circ_83543,RMVar_hsa_circ_132180,RMVar_hsa_circ_121465,RMVar_hsa_circ_117381,RMVar_hsa_circ_132182,RMVar_hsa_circ_132183 31469 RMVar_ID_31469 Human_SNP_ID_11051500 A-to-I Human chr1 + 42673194 42673194 42673194 CTTTTTAGAGATGGGGTTTCACCATGTTGTCCAGGCCGGTCTCAAACTCCTGGCTTCAAGCGATC CTTTTTAGAGATGGGGTTTCACCATGTTGTCCGGGCCGGTCTCAAACTCCTGGCTTCAAGCGATC A G PPIH Ensembl:ENSG00000171960 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1416508250 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10993141 RMVar_hsa_circ_102044,RMVar_hsa_circ_132175,RMVar_hsa_circ_88700,RMVar_hsa_circ_101370,RMVar_hsa_circ_132176,RMVar_hsa_circ_132178,RMVar_hsa_circ_83543,RMVar_hsa_circ_132180,RMVar_hsa_circ_121465,RMVar_hsa_circ_117381,RMVar_hsa_circ_132182,RMVar_hsa_circ_132183 31470 RMVar_ID_31470 Human_SNP_ID_11055476 A-to-I Human chr1 + 42687983 42687983 42687983 GGTTCCAAACTGGAACCCTAAAGACAAACATCAATGACATGTATGCAGGAGACATTAGGAGAGAT GGTTCCAAACTGGAACCCTAAAGACAAACATCGATGACATGTATGCAGGAGACATTAGGAGAGAT A G YBX1 Ensembl:ENSG00000065978 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs891964028 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10993575 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 31471 RMVar_ID_31471 Human_SNP_ID_11056062 A-to-I Human chr1 + 42690145 42690145 42690145 GGCTGAAGTGCAAGAACTTGAACCCCGAAGGCAGAGGTTGCAGTGAGCCAAGATCGCTACTGCAC GGCTGAAGTGCAAGAACTTGAACCCCGAAGGCGGAGGTTGCAGTGAGCCAAGATCGCTACTGCAC A G YBX1 Ensembl:ENSG00000065978 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs146022145 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5827073,Human_RBP_ID_10993709 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 31472 RMVar_ID_31472 Human_SNP_ID_11074920 A-to-I Human chr1 - 42760052 42760052 42760052 TGAACCCTGGAGGCGGATGTTGCAGTGAGCCAAGATCGCACTATTGCACTCTAGCCTGGGCAACA TGAACCCTGGAGGCGGATGTTGCAGTGAGCCAGGATCGCACTATTGCACTCTAGCCTGGGCAACA T C P3H1 Ensembl:ENSG00000117385 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1429284109 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19899,RMVar_hsa_circ_111496,RMVar_hsa_circ_132194,RMVar_hsa_circ_28580,RMVar_hsa_circ_38913,RMVar_hsa_circ_73094,RMVar_hsa_circ_303285,RMVar_hsa_circ_42516 31473 RMVar_ID_31473 Human_SNP_ID_11079429 A-to-I Human chr1 + 42777225 42777225 42777225 TCAAGTGATTCTCCTGCCTCAGCCTCCTCAGTAGCTGAGATTACAGGCGCACGCCACCATGCCCA TCAAGTGATTCTCCTGCCTCAGCCTCCTCAGTCGCTGAGATTACAGGCGCACGCCACCATGCCCA A C AC098484.3,C1orf50 Ensembl:ENSG00000283580,Ensembl:ENSG00000164008 Protein coding,Protein coding intron,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs990458777 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_132207,RMVar_hsa_circ_132213 31474 RMVar_ID_31474 Human_SNP_ID_11079448 A-to-I Human chr1 + 42777296 42777296 42777296 TTTTTTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGAGGGTCTCTATCTCTTGACCT TTTTTTATTTTTAGTAGAGACAGGGTTTCACCGTGTTGGCCAGGAGGGTCTCTATCTCTTGACCT A G AC098484.3,C1orf50 Ensembl:ENSG00000283580,Ensembl:ENSG00000164008 Protein coding,Protein coding intron,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs890365103 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_132207,RMVar_hsa_circ_132213 31475 RMVar_ID_31475 Human_SNP_ID_11079456 A-to-I Human chr1 + 42777330 42777330 42777330 GTTGGCCAGGAGGGTCTCTATCTCTTGACCTCATGATCCACCTGCCTCAGCCTCCCACAGTGCTG GTTGGCCAGGAGGGTCTCTATCTCTTGACCTCCTGATCCACCTGCCTCAGCCTCCCACAGTGCTG A C AC098484.3,C1orf50 Ensembl:ENSG00000283580,Ensembl:ENSG00000164008 Protein coding,Protein coding intron,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1271848862 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_132207,RMVar_hsa_circ_132213 31476 RMVar_ID_31476 Human_SNP_ID_11080096 A-to-I Human chr1 + 42780166 42780165 42780166 ACTGTGTTACTCAGGCTGGAGAGCAGTAGCTCAGTCATAGCCCACTGCAGCCTTGAACTCCTGGG ACTGTGTTACTCAGGCTGGAGAGCAGTAGCTC_GTCATAGCCCACTGCAGCCTTGAACTCCTGGG CA C AC098484.3 Ensembl:ENSG00000283580 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1482486888 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_132207,RMVar_hsa_circ_132213 31477 RMVar_ID_31477 Human_SNP_ID_11080141 A-to-I Human chr1 + 42780321 42780321 42780321 TAGAGATGAAGACTCACCATGTTGCCCAGGCTAGTCCCAAATTCCTGGCCTCAAGCAGAATAAGA TAGAGATGAAGACTCACCATGTTGCCCAGGCTGGTCCCAAATTCCTGGCCTCAAGCAGAATAAGA A G AC098484.3 Ensembl:ENSG00000283580 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs905291627 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_132207,RMVar_hsa_circ_132213 31478 RMVar_ID_31478 Human_SNP_ID_11085917 A-to-I Human chr1 - 42805571 42805571 42805571 GACTTTGTTGCCCAGGCTGGTCTCAAACTCCTAGCTCAAGTGATCCACCCGCCTCAGCCTCGCAA GACTTTGTTGCCCAGGCTGGTCTCAAACTCCTGGCTCAAGTGATCCACCCGCCTCAGCCTCGCAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1410915020 Functional Loss SNV dbSNP153 33..33 33 - - - 31479 RMVar_ID_31479 Human_SNP_ID_11090020 A-to-I Human chr1 + 42821928 42821927 42821928 CTAGCTACTAGGGAGACTGAGGCAAGAGGATCACTTGAGCCTAGGAGTTCAAGGCTGCAGTGAGC CTAGCTACTAGGGAGACTGAGGCAAGAGGATC_CTTGAGCCTAGGAGTTCAAGGCTGCAGTGAGC CA C ERMAP Ensembl:ENSG00000164010 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1171296031 Functional Loss DEL dbSNP153 33..33 33 - - - 31480 RMVar_ID_31480 Human_SNP_ID_11090989 A-to-I Human chr1 + 42826596 42826596 42826596 TTACAAAGTCATGGCTGGGCGCAGTGGCTCACACCTGTAATCCCAACACTTTGGGGGGCCGAGGA TTACAAAGTCATGGCTGGGCGCAGTGGCTCACGCCTGTAATCCCAACACTTTGGGGGGCCGAGGA A G ERMAP Ensembl:ENSG00000164010 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1380144412 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_30 31481 RMVar_ID_31481 Human_SNP_ID_11124535 A-to-I Human chr1 + 42960223 42960223 42960223 AGTCTGTTAGTAAATAAATAAATGCTGGTCTCAAACTCCTGGGCTCAAGTGATCCTCCCACCTTA AGTCTGTTAGTAAATAAATAAATGCTGGTCTCGAACTCCTGGGCTCAAGTGATCCTCCCACCTTA A G SLC2A1-AS1 Ensembl:ENSG00000227533 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs907079857 Functional Loss SNV dbSNP153 33..33 33 - - - 31482 RMVar_ID_31482 Human_SNP_ID_11127123 A-to-I Human chr1 + 42971380 42971380 42971380 CCAAGGTGGGCATATCACGAGGTCAAGAGATCAAGACCATCCTGGCCAATGTGGTAAAACCCCGT CCAAGGTGGGCATATCACGAGGTCAAGAGATCCAGACCATCCTGGCCAATGTGGTAAAACCCCGT A C SLC2A1-AS1 Ensembl:ENSG00000227533 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017126284 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_132223,RMVar_hsa_circ_345263 31483 RMVar_ID_31483 Human_SNP_ID_11127124 A-to-I Human chr1 + 42971380 42971380 42971380 CCAAGGTGGGCATATCACGAGGTCAAGAGATCAAGACCATCCTGGCCAATGTGGTAAAACCCCGT CCAAGGTGGGCATATCACGAGGTCAAGAGATCGAGACCATCCTGGCCAATGTGGTAAAACCCCGT A G SLC2A1-AS1 Ensembl:ENSG00000227533 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017126284 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_132223,RMVar_hsa_circ_345263 31484 RMVar_ID_31484 Human_SNP_ID_11132315 A-to-I Human chr1 + 42993135 42993135 42993135 AGCCAGGCGTGTTGGTGGGTGCCTGTAGTCCCAGCTACTGGGGAGGCTGAGACAGGATAATGGCG AGCCAGGCGTGTTGGTGGGTGCCTGTAGTCCCGGCTACTGGGGAGGCTGAGACAGGATAATGGCG A G SLC2A1-AS1 Ensembl:ENSG00000227533 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs948049949 Functional Loss SNV dbSNP153 33..33 33 - - - 31485 RMVar_ID_31485 Human_SNP_ID_11226677 A-to-I Human chr1 - 43384301 43384301 43384301 AAGTGGCTCTGCCAGGCAGGACTATGTGGGAAAGGGTTTTTCCTTAGCACACGAAAAAGCCCCTT AAGTGGCTCTGCCAGGCAGGACTATGTGGGAAGGGGTTTTTCCTTAGCACACGAAAAAGCCCCTT T C MED8 Ensembl:ENSG00000159479 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs576231216 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_978480,Human_RBP_ID_5827917,Human_RBP_ID_8168001,Human_RBP_ID_8311945 31486 RMVar_ID_31486 Human_SNP_ID_11231011 A-to-I Human chr1 + 43400945 43400944 43400946 ACTGTAATAAATAGTTAACTTTTTTTTTGGACAGGGTCTCGCTCTGTTGCTCAGGCTGGAGTGCC ACTGTAATAAATAGTTAACTTTTTTTTTGGAC__GGTCTCGCTCTGTTGCTCAGGCTGGAGTGCC CAG C SZT2 Ensembl:ENSG00000198198 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1162430768 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_132252,RMVar_hsa_circ_78794 31487 RMVar_ID_31487 Human_SNP_ID_11232528 A-to-I Human chr1 + 43407270 43407270 43407270 TCATGCCTGTAATCCTAGCACTTTGGGAAGCCAAGGCAGGTGAATCACATGAGGCCAAGCGTTTG TCATGCCTGTAATCCTAGCACTTTGGGAAGCCTAGGCAGGTGAATCACATGAGGCCAAGCGTTTG A T SZT2 Ensembl:ENSG00000198198 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs752434397 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45653,RMVar_hsa_circ_132252,RMVar_hsa_circ_78794,RMVar_hsa_circ_267353,RMVar_hsa_circ_95800,RMVar_hsa_circ_132254,RMVar_hsa_circ_89942,RMVar_hsa_circ_112611,RMVar_hsa_circ_132255,RMVar_hsa_circ_132256 31488 RMVar_ID_31488 Human_SNP_ID_11233212 A-to-I Human chr1 + 43410297 43410297 43410297 AAATCTGGCCAGGCGCAGTGGCTCACACCTGTAATCCCAACACTTTGGGAGGCCAAGGCAGGTGG AAATCTGGCCAGGCGCAGTGGCTCACACCTGTGATCCCAACACTTTGGGAGGCCAAGGCAGGTGG A G SZT2 Ensembl:ENSG00000198198 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1222490137 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45653,RMVar_hsa_circ_132252,RMVar_hsa_circ_78794,RMVar_hsa_circ_267353,RMVar_hsa_circ_95800,RMVar_hsa_circ_132254,RMVar_hsa_circ_89942,RMVar_hsa_circ_112611,RMVar_hsa_circ_132255,RMVar_hsa_circ_132256 31489 RMVar_ID_31489 Human_SNP_ID_11233623 A-to-I Human chr1 + 43411918 43411918 43411918 CTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCACCTGCCACTACGCCCAGCTAATGTTT CTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTGCAGGCACCTGCCACTACGCCCAGCTAATGTTT A G SZT2 Ensembl:ENSG00000198198 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1451136292 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45653,RMVar_hsa_circ_132252,RMVar_hsa_circ_78794,RMVar_hsa_circ_267353,RMVar_hsa_circ_95800,RMVar_hsa_circ_132254,RMVar_hsa_circ_89942,RMVar_hsa_circ_112611,RMVar_hsa_circ_132255,RMVar_hsa_circ_132256 31490 RMVar_ID_31490 Human_SNP_ID_11233730 A-to-I Human chr1 + 43412365 43412361 43412366 TTGCCTGGGCTGGAGTGCAGTGGTGTGAACACAGCTCACTGCAGCCTTGATCTCTTGGGCTTAAG TTGCCTGGGCTGGAGTGCAGTGGTGTGAA_____CTCACTGCAGCCTTGATCTCTTGGGCTTAAG ACACAG A SZT2 Ensembl:ENSG00000198198 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs771548010 Functional Loss DEL dbSNP153 30..34 33 - - - RMVar_hsa_circ_45653,RMVar_hsa_circ_132252,RMVar_hsa_circ_78794,RMVar_hsa_circ_267353,RMVar_hsa_circ_95800,RMVar_hsa_circ_132254,RMVar_hsa_circ_89942,RMVar_hsa_circ_112611,RMVar_hsa_circ_132255,RMVar_hsa_circ_132256 31491 RMVar_ID_31491 Human_SNP_ID_11233929 A-to-I Human chr1 + 43413262 43413262 43413262 AAAATTAGCTGAGCGTGATGGCAGATGCCTGTAATCCCAGCTACTCGGGAGCCTGAGGCAGAGAA AAAATTAGCTGAGCGTGATGGCAGATGCCTGTCATCCCAGCTACTCGGGAGCCTGAGGCAGAGAA A C SZT2 Ensembl:ENSG00000198198 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1300053877 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45653,RMVar_hsa_circ_132252,RMVar_hsa_circ_78794,RMVar_hsa_circ_267353,RMVar_hsa_circ_95800,RMVar_hsa_circ_132254,RMVar_hsa_circ_89942,RMVar_hsa_circ_112611,RMVar_hsa_circ_132255,RMVar_hsa_circ_132256 31492 RMVar_ID_31492 Human_SNP_ID_11233932 A-to-I Human chr1 + 43413272 43413272 43413272 GAGCGTGATGGCAGATGCCTGTAATCCCAGCTACTCGGGAGCCTGAGGCAGAGAATTGCTTGAAT GAGCGTGATGGCAGATGCCTGTAATCCCAGCTCCTCGGGAGCCTGAGGCAGAGAATTGCTTGAAT A C SZT2 Ensembl:ENSG00000198198 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1433144157 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45653,RMVar_hsa_circ_132252,RMVar_hsa_circ_78794,RMVar_hsa_circ_267353,RMVar_hsa_circ_95800,RMVar_hsa_circ_132254,RMVar_hsa_circ_89942,RMVar_hsa_circ_112611,RMVar_hsa_circ_132255,RMVar_hsa_circ_132256 31493 RMVar_ID_31493 Human_SNP_ID_11241261 A-to-I Human chr1 + 43438361 43438361 43438361 AGGTGTCCAGTAGGCAACTGGATTTTCCAGCTAATATTTATAGCTCAATTAACATGTGCTGGTCT AGGTGTCCAGTAGGCAACTGGATTTTCCAGCTTATATTTATAGCTCAATTAACATGTGCTGGTCT A T SZT2 Ensembl:ENSG00000198198 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031005439 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124065,RMVar_hsa_circ_115278,RMVar_hsa_circ_132264,RMVar_hsa_circ_132266,RMVar_hsa_circ_266034,RMVar_hsa_circ_120156,RMVar_hsa_circ_110105,RMVar_hsa_circ_8420,RMVar_hsa_circ_132281,RMVar_hsa_circ_132282,RMVar_hsa_circ_27013,RMVar_hsa_circ_26179 31494 RMVar_ID_31494 Human_SNP_ID_11281934 A-to-I Human chr1 - 43593903 43593903 43593903 CGGCTCACTGCAACCTCTGCCTGCTGGGGTCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTATGT CGGCTCACTGCAACCTCTGCCTGCTGGGGTCAGGTGATTCTCCTGCCTCAGCCTCCCGAGTATGT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs952289038 Functional Loss SNV dbSNP153 33..33 33 - - - 31495 RMVar_ID_31495 Human_SNP_ID_11300808 A-to-I Human chr1 + 43659039 43659039 43659039 TATTTTTAGACTGGGTGCATTGGCTAACTTCTATAATCCCATCACTTTGGGAGGCCGAGGTTGGA TATTTTTAGACTGGGTGCATTGGCTAACTTCTGTAATCCCATCACTTTGGGAGGCCGAGGTTGGA A G KDM4A,AL451062.4 Ensembl:ENSG00000066135,Ensembl:ENSG00000284989 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1011410793 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10996908 RMVar_hsa_circ_11888,RMVar_hsa_circ_324177,RMVar_hsa_circ_338033,RMVar_hsa_circ_355215,RMVar_hsa_circ_329090,RMVar_hsa_circ_287518,RMVar_hsa_circ_19285,RMVar_hsa_circ_10640,RMVar_hsa_circ_132321,RMVar_hsa_circ_132322,RMVar_hsa_circ_265841,RMVar_hsa_circ_322392,RMVar_hsa_circ_348339,RMVar_hsa_circ_96119,RMVar_hsa_circ_132323 31496 RMVar_ID_31496 Human_SNP_ID_11301324 A-to-I Human chr1 + 43661175 43661175 43661175 TTTGTATTTTTTAGTAGAGACGGGGTTTCTCCATGTTGCTCAGGCTGGTTTTAAACTCCCGACCT TTTGTATTTTTTAGTAGAGACGGGGTTTCTCCCTGTTGCTCAGGCTGGTTTTAAACTCCCGACCT A C KDM4A,AL451062.4 Ensembl:ENSG00000066135,Ensembl:ENSG00000284989 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1415717042 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11888,RMVar_hsa_circ_324177,RMVar_hsa_circ_338033,RMVar_hsa_circ_355215,RMVar_hsa_circ_329090,RMVar_hsa_circ_19285,RMVar_hsa_circ_10640,RMVar_hsa_circ_132322,RMVar_hsa_circ_265841,RMVar_hsa_circ_348339,RMVar_hsa_circ_96119,RMVar_hsa_circ_112236,RMVar_hsa_circ_132323,RMVar_hsa_circ_349409,RMVar_hsa_circ_132324 31497 RMVar_ID_31497 Human_SNP_ID_11301325 A-to-I Human chr1 + 43661175 43661175 43661175 TTTGTATTTTTTAGTAGAGACGGGGTTTCTCCATGTTGCTCAGGCTGGTTTTAAACTCCCGACCT TTTGTATTTTTTAGTAGAGACGGGGTTTCTCCGTGTTGCTCAGGCTGGTTTTAAACTCCCGACCT A G KDM4A,AL451062.4 Ensembl:ENSG00000066135,Ensembl:ENSG00000284989 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1415717042 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11888,RMVar_hsa_circ_324177,RMVar_hsa_circ_338033,RMVar_hsa_circ_355215,RMVar_hsa_circ_329090,RMVar_hsa_circ_19285,RMVar_hsa_circ_10640,RMVar_hsa_circ_132322,RMVar_hsa_circ_265841,RMVar_hsa_circ_348339,RMVar_hsa_circ_96119,RMVar_hsa_circ_112236,RMVar_hsa_circ_132323,RMVar_hsa_circ_349409,RMVar_hsa_circ_132324 31498 RMVar_ID_31498 Human_SNP_ID_11301705 A-to-I Human chr1 + 43662487 43662485 43662488 AAAATTAGTTGGGCATGGTGGTGGGTGCCTGTAATCCCAGGTGCGCGGGAGGCTGAAGCAGGGAA AAAATTAGTTGGGCATGGTGGTGGGTGCCTG___TCCCAGGTGCGCGGGAGGCTGAAGCAGGGAA GTAA G KDM4A,AL451062.4 Ensembl:ENSG00000066135,Ensembl:ENSG00000284989 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1361920315 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_95675 RMVar_hsa_circ_11888,RMVar_hsa_circ_324177,RMVar_hsa_circ_338033,RMVar_hsa_circ_355215,RMVar_hsa_circ_329090,RMVar_hsa_circ_19285,RMVar_hsa_circ_10640,RMVar_hsa_circ_132322,RMVar_hsa_circ_265841,RMVar_hsa_circ_348339,RMVar_hsa_circ_96119,RMVar_hsa_circ_112236,RMVar_hsa_circ_132323,RMVar_hsa_circ_349409,RMVar_hsa_circ_132324 31499 RMVar_ID_31499 Human_SNP_ID_11305167 A-to-I Human chr1 + 43676231 43676231 43676231 AGAATTGCTTGAGCCTGAGAGGTTGAGGCTGCAATGAGCCGTGACTGTACCATTGCACTACAGCC AGAATTGCTTGAGCCTGAGAGGTTGAGGCTGCTATGAGCCGTGACTGTACCATTGCACTACAGCC A T KDM4A,AL451062.4 Ensembl:ENSG00000066135,Ensembl:ENSG00000284989 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1336292388 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557141 RMVar_hsa_circ_10387,RMVar_hsa_circ_11888,RMVar_hsa_circ_355215,RMVar_hsa_circ_19285,RMVar_hsa_circ_265841,RMVar_hsa_circ_96119,RMVar_hsa_circ_69339,RMVar_hsa_circ_132323,RMVar_hsa_circ_373060,RMVar_hsa_circ_44617,RMVar_hsa_circ_132326,RMVar_hsa_circ_132327,RMVar_hsa_circ_106359,RMVar_hsa_circ_15188,RMVar_hsa_circ_327592,RMVar_hsa_circ_365052,RMVar_hsa_circ_132329 31500 RMVar_ID_31500 Human_SNP_ID_11321038 A-to-I Human chr1 + 43741206 43741206 43741206 AAAAAATTAGCTGAATGTGGTGGTACATGTCTATGGTGCCAGCTACTCGAGAGGCTGAGGTGGGA AAAAAATTAGCTGAATGTGGTGGTACATGTCTGTGGTGCCAGCTACTCGAGAGGCTGAGGTGGGA A G AL451062.4,ST3GAL3 Ensembl:ENSG00000284989,Ensembl:ENSG00000126091 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1222249700 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18575715 RMVar_hsa_circ_44622,RMVar_hsa_circ_302489,RMVar_hsa_circ_40044,RMVar_hsa_circ_40460 31501 RMVar_ID_31501 Human_SNP_ID_11324258 A-to-I Human chr1 + 43754372 43754372 43754372 CAAGCACCCCATCCGGCTAATTTTTGTATTTTAGTAGAGACGAGGTTTCACCGCGTTAGCCAGGC CAAGCACCCCATCCGGCTAATTTTTGTATTTTGGTAGAGACGAGGTTTCACCGCGTTAGCCAGGC A G AL451062.4,ST3GAL3 Ensembl:ENSG00000284989,Ensembl:ENSG00000126091 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs969885112 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44622,RMVar_hsa_circ_302489,RMVar_hsa_circ_40044,RMVar_hsa_circ_40460 31502 RMVar_ID_31502 Human_SNP_ID_11324267 A-to-I Human chr1 + 43754401 43754401 43754401 TTTAGTAGAGACGAGGTTTCACCGCGTTAGCCAGGCTGGTCTCTAACTCCTGACCTCAAGCAATC TTTAGTAGAGACGAGGTTTCACCGCGTTAGCCGGGCTGGTCTCTAACTCCTGACCTCAAGCAATC A G AL451062.4,ST3GAL3 Ensembl:ENSG00000284989,Ensembl:ENSG00000126091 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1018269840 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44622,RMVar_hsa_circ_302489,RMVar_hsa_circ_40044,RMVar_hsa_circ_40460 31503 RMVar_ID_31503 Human_SNP_ID_11325139 A-to-I Human chr1 + 43758330 43758330 43758330 TGGAGTGCAGTGGTGCAATTATAGTTCACTGCAACCTCAAAGTCCTGGGCTCAGGCAATCCTCCC TGGAGTGCAGTGGTGCAATTATAGTTCACTGCCACCTCAAAGTCCTGGGCTCAGGCAATCCTCCC A C AL451062.4,ST3GAL3 Ensembl:ENSG00000284989,Ensembl:ENSG00000126091 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs988349446 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10998567 RMVar_hsa_circ_44622,RMVar_hsa_circ_302489,RMVar_hsa_circ_40044,RMVar_hsa_circ_40460 31504 RMVar_ID_31504 Human_SNP_ID_11325140 A-to-I Human chr1 + 43758330 43758330 43758330 TGGAGTGCAGTGGTGCAATTATAGTTCACTGCAACCTCAAAGTCCTGGGCTCAGGCAATCCTCCC TGGAGTGCAGTGGTGCAATTATAGTTCACTGCTACCTCAAAGTCCTGGGCTCAGGCAATCCTCCC A T AL451062.4,ST3GAL3 Ensembl:ENSG00000284989,Ensembl:ENSG00000126091 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs988349446 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10998567 RMVar_hsa_circ_44622,RMVar_hsa_circ_302489,RMVar_hsa_circ_40044,RMVar_hsa_circ_40460 31505 RMVar_ID_31505 Human_SNP_ID_11352113 A-to-I Human chr1 + 43876153 43876153 43876153 GCAGGATAATTTTTTAAATTTTTTGTAGAGACAGGGTTTCGCCATGTTGCTCAGGCTGATCTCAA GCAGGATAATTTTTTAAATTTTTTGTAGAGACGGGGTTTCGCCATGTTGCTCAGGCTGATCTCAA A G AL451062.4,ST3GAL3 Ensembl:ENSG00000284989,Ensembl:ENSG00000126091 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs945809169 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 31506 RMVar_ID_31506 Human_SNP_ID_11355375 A-to-I Human chr1 + 43890799 43890799 43890799 CTAGCTACTCGGGAGGCTGAGGTGGGAGGATCACTTGAGCCCAGGAGTTTGGGATTACAGTGAGC CTAGCTACTCGGGAGGCTGAGGTGGGAGGATCCCTTGAGCCCAGGAGTTTGGGATTACAGTGAGC A C AL451062.4,ST3GAL3 Ensembl:ENSG00000284989,Ensembl:ENSG00000126091 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1015327090 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_96719 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 31507 RMVar_ID_31507 Human_SNP_ID_11355376 A-to-I Human chr1 + 43890799 43890799 43890799 CTAGCTACTCGGGAGGCTGAGGTGGGAGGATCACTTGAGCCCAGGAGTTTGGGATTACAGTGAGC CTAGCTACTCGGGAGGCTGAGGTGGGAGGATCGCTTGAGCCCAGGAGTTTGGGATTACAGTGAGC A G AL451062.4,ST3GAL3 Ensembl:ENSG00000284989,Ensembl:ENSG00000126091 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1015327090 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_96719 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 31508 RMVar_ID_31508 Human_SNP_ID_11362086 A-to-I Human chr1 + 43916827 43916827 43916827 GAATTCCTGGGCTCAAGTAATCCTCTCACCTCAGCCTGCCAAAGTGCTAGGATTACAGGCATGAG GAATTCCTGGGCTCAAGTAATCCTCTCACCTCTGCCTGCCAAAGTGCTAGGATTACAGGCATGAG A T AL451062.4,ST3GAL3 Ensembl:ENSG00000284989,Ensembl:ENSG00000126091 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1197914896 Functional Loss SNV dbSNP153 33..33 33 - - - 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 31509 RMVar_ID_31509 Human_SNP_ID_11368481 A-to-I Human chr1 - 43940561 43940561 43940561 TTTTATATTTTTAGTAGAGACCGGGTTTTACCATGTTGGCTAGGGTGGTCTCACTCTCTTGACCT TTTTATATTTTTAGTAGAGACCGGGTTTTACCGTGTTGGCTAGGGTGGTCTCACTCTCTTGACCT T C AL357079.1 Ensembl:ENSG00000237950 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs368743399 Functional Loss SNV dbSNP153 33..33 33 - - - 31510 RMVar_ID_31510 Human_SNP_ID_11368486 A-to-I Human chr1 - 43940581 43940581 43940581 TGCCACCACGCCCAGCTAATTTTTATATTTTTAGTAGAGACCGGGTTTTACCATGTTGGCTAGGG TGCCACCACGCCCAGCTAATTTTTATATTTTTGGTAGAGACCGGGTTTTACCATGTTGGCTAGGG T C AL357079.1 Ensembl:ENSG00000237950 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1385643343 Functional Loss SNV dbSNP153 33..33 33 - - - 31511 RMVar_ID_31511 Human_SNP_ID_11380321 A-to-I Human chr1 + 43986203 43986203 43986203 GGTGTGTGAAATGTAAACAAGGGCTTCCTGACACTGCTCTGACTTGTGCTAAACTTTCTGGGGGT GGTGTGTGAAATGTAAACAAGGGCTTCCTGACGCTGCTCTGACTTGTGCTAAACTTTCTGGGGGT A G B4GALT2 Ensembl:ENSG00000117411 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs914285762 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_356064 31512 RMVar_ID_31512 Human_SNP_ID_11380548 A-to-I Human chr1 + 43987309 43987309 43987309 AACTCTGTGAATGTTGGATTCATGGATTGGGTATGACTACTCTGGGTCTGCCACCCCCAGAAAGT AACTCTGTGAATGTTGGATTCATGGATTGGGTGTGACTACTCTGGGTCTGCCACCCCCAGAAAGT A G B4GALT2 Ensembl:ENSG00000117411 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs963343476 Functional Loss SNV dbSNP153 33..33 33 - - - 31513 RMVar_ID_31513 Human_SNP_ID_11382777 A-to-I Human chr1 + 43994188 43994188 43994188 GATGCCACGGCCGAGCATGATGGTGCATGCCTATAATCCCAGCAATTTGGGAGGCCGAGGCAAGA GATGCCACGGCCGAGCATGATGGTGCATGCCTGTAATCCCAGCAATTTGGGAGGCCGAGGCAAGA A G CCDC24 Ensembl:ENSG00000159214 Protein coding 3'UTR GSE100210;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229 RNA-Seq:(High) rs1362835511 Functional Loss SNV dbSNP153 33..33 33 - - - 31514 RMVar_ID_31514 Human_SNP_ID_11382795 A-to-I Human chr1 - 43994263 43994263 43994263 TGTATTTGTTTTGGTAGAGATGGGGTTTTCCCATGTTGGCCAAGCTGGTTTCGAATTCCTGGGCC TGTATTTGTTTTGGTAGAGATGGGGTTTTCCCGTGTTGGCCAAGCTGGTTTCGAATTCCTGGGCC T C SLC6A9 Ensembl:ENSG00000196517 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910045495 Functional Loss SNV dbSNP153 33..33 33 - - - 31515 RMVar_ID_31515 Human_SNP_ID_11382911 A-to-I Human chr1 + 43994582 43994582 43994582 CCTGCCTAAGCCTCCCGAGTAGCTGGGACTACAGATGCCCACCACCATGCCCAGCTAATTTTTTT CCTGCCTAAGCCTCCCGAGTAGCTGGGACTACGGATGCCCACCACCATGCCCAGCTAATTTTTTT A G CCDC24 Ensembl:ENSG00000159214 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1477708147 Functional Loss SNV dbSNP153 33..33 33 - - - 31516 RMVar_ID_31516 Human_SNP_ID_11403362 A-to-I Human chr1 + 44076811 44076811 44076811 CAGTGATGTAATAATAGCTCACTGAAACCTCGAACTCCTGGGCTCAAGCAATTATCCCATCTCGG CAGTGATGTAATAATAGCTCACTGAAACCTCGGACTCCTGGGCTCAAGCAATTATCCCATCTCGG A G AL139220.2 Ensembl:ENSG00000230615 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1275808258 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_61226 RMVar_hsa_circ_35479 31517 RMVar_ID_31517 Human_SNP_ID_11405865 A-to-I Human chr1 + 44086280 44086280 44086280 CCTGAGATCGGGAGTTTGTGACCAGGCTGAGCAACATGGAGAAACCCCGTCTCTACTAAAAGTAC CCTGAGATCGGGAGTTTGTGACCAGGCTGAGCGACATGGAGAAACCCCGTCTCTACTAAAAGTAC A G AL139220.2 Ensembl:ENSG00000230615 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1473946770 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35479 31518 RMVar_ID_31518 Human_SNP_ID_11405866 A-to-I Human chr1 + 44086280 44086280 44086280 CCTGAGATCGGGAGTTTGTGACCAGGCTGAGCAACATGGAGAAACCCCGTCTCTACTAAAAGTAC CCTGAGATCGGGAGTTTGTGACCAGGCTGAGCTACATGGAGAAACCCCGTCTCTACTAAAAGTAC A T AL139220.2 Ensembl:ENSG00000230615 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1473946770 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35479 31519 RMVar_ID_31519 Human_SNP_ID_11406157 A-to-I Human chr1 + 44087464 44087464 44087464 AAAAAAATTTTTTTTAAAGACAGGGTCTCCCTATGTTGCCTAGGCTGGTTTCAAACTCTTGACCT AAAAAAATTTTTTTTAAAGACAGGGTCTCCCTGTGTTGCCTAGGCTGGTTTCAAACTCTTGACCT A G AL139220.2 Ensembl:ENSG00000230615 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1302620400 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35479 31520 RMVar_ID_31520 Human_SNP_ID_11406922 A-to-I Human chr1 + 44090000 44090000 44090000 CCTGGCCAACATGGTGAAAACCTGTCCCTACTAAAAATGCAAAAAGTTAGCCGGGCGTACTCGGG CCTGGCCAACATGGTGAAAACCTGTCCCTACTTAAAATGCAAAAAGTTAGCCGGGCGTACTCGGG A T AL139220.2 Ensembl:ENSG00000230615 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1454729609 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35479 31521 RMVar_ID_31521 Human_SNP_ID_11406948 A-to-I Human chr1 + 44090092 44090092 44090092 CTGGGAGATCAAGGCTGCAGTGAGCTCTGACCATGCCACTGCCTGGGTGATAAAGTGAGACTCTG CTGGGAGATCAAGGCTGCAGTGAGCTCTGACCCTGCCACTGCCTGGGTGATAAAGTGAGACTCTG A C AL139220.2 Ensembl:ENSG00000230615 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1381432563 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35479 31522 RMVar_ID_31522 Human_SNP_ID_11407368 A-to-I Human chr1 + 44091446 44091446 44091446 GAGAGCCTGATGCAGGTGGATCATTTGAGGTCAGGAGTTTGAGACCAACTTGGCCAACCTGGTGA GAGAGCCTGATGCAGGTGGATCATTTGAGGTCGGGAGTTTGAGACCAACTTGGCCAACCTGGTGA A G AL139220.2 Ensembl:ENSG00000230615 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs921616412 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35479 31523 RMVar_ID_31523 Human_SNP_ID_11407386 A-to-I Human chr1 + 44091491 44091491 44091491 CAACTTGGCCAACCTGGTGAGACCCTGTTTCTACTAAAAACATGAGAATTAGCCAGGCATGGTGG CAACTTGGCCAACCTGGTGAGACCCTGTTTCTTCTAAAAACATGAGAATTAGCCAGGCATGGTGG A T AL139220.2 Ensembl:ENSG00000230615 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1180873196 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35479 31524 RMVar_ID_31524 Human_SNP_ID_11411840 A-to-I Human chr1 + 44107366 44107366 44107366 ACCTTAGGTTATCCACCCGCCTCGGCTTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCGC ACCTTAGGTTATCCACCCGCCTCGGCTTCCCAGAGTGCTGGGATTACAGGTGTGAGCCACCGCGC A G AL139220.2 Ensembl:ENSG00000230615 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1428641905 Functional Loss SNV dbSNP153 33..33 33 - - - 31525 RMVar_ID_31525 Human_SNP_ID_11412573 A-to-I Human chr1 + 44110457 44110457 44110457 TCATGCCTGTAATCCCAGTGCTTTGGGAGTCCAAGGCGGGCAGATCAACTGACGTCAGGGGTTCG TCATGCCTGTAATCCCAGTGCTTTGGGAGTCCCAGGCGGGCAGATCAACTGACGTCAGGGGTTCG A C AL139220.2 Ensembl:ENSG00000230615 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs937420543 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_61246 31526 RMVar_ID_31526 Human_SNP_ID_11413729 A-to-I Human chr1 + 44115308 44115308 44115308 ACTACAAATACACACACACAAAAAAATTAGCCAAGAGTGGTGGCAGGCGCCTGTAGTCACAGCTA ACTACAAATACACACACACAAAAAAATTAGCCGAGAGTGGTGGCAGGCGCCTGTAGTCACAGCTA A G AL139220.2 Ensembl:ENSG00000230615 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1235409625 Functional Loss SNV dbSNP153 33..33 33 - - - 31527 RMVar_ID_31527 Human_SNP_ID_11413739 A-to-I Human chr1 + 44115330 44115330 44115330 AAAATTAGCCAAGAGTGGTGGCAGGCGCCTGTAGTCACAGCTACTTGGGAGGCTGAGGCAGGAGA AAAATTAGCCAAGAGTGGTGGCAGGCGCCTGTGGTCACAGCTACTTGGGAGGCTGAGGCAGGAGA A G AL139220.2 Ensembl:ENSG00000230615 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs969550359 Functional Loss SNV dbSNP153 33..33 33 - - - 31528 RMVar_ID_31528 Human_SNP_ID_11413741 A-to-I Human chr1 + 44115340 44115340 44115340 AAGAGTGGTGGCAGGCGCCTGTAGTCACAGCTACTTGGGAGGCTGAGGCAGGAGAATGGCATGAA AAGAGTGGTGGCAGGCGCCTGTAGTCACAGCTGCTTGGGAGGCTGAGGCAGGAGAATGGCATGAA A G AL139220.2 Ensembl:ENSG00000230615 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs568115416 Functional Loss SNV dbSNP153 33..33 33 - - - 31529 RMVar_ID_31529 Human_SNP_ID_11435528 A-to-I Human chr1 - 44204796 44204796 44204796 ATGGTGATATGCACCTGTAGTCCTAGCTACTCAGAAGCCTGAGGCAGGAGGATTGCCTGAGCCCA ATGGTGATATGCACCTGTAGTCCTAGCTACTCGGAAGCCTGAGGCAGGAGGATTGCCTGAGCCCA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1455238963 Functional Loss SNV dbSNP153 33..33 33 - - - 31530 RMVar_ID_31530 Human_SNP_ID_11442034 A-to-I Human chr1 - 44231465 44231465 44231465 GGAGGCTGATGCAGGAGGATTGCTTGACCCCAAGAGGTCGAGACTGTGGTGAGCTATGAGCAAAC GGAGGCTGATGCAGGAGGATTGCTTGACCCCAGGAGGTCGAGACTGTGGTGAGCTATGAGCAAAC T C ERI3 Ensembl:ENSG00000117419 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1381906804 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11000161 31531 RMVar_ID_31531 Human_SNP_ID_11442755 A-to-I Human chr1 - 44234602 44234602 44234602 CCGGCTAGAGTGCAGTGATGTGATCTCGGCTCACTGCAACCTCCGCCTCCTGTTTTCAAGTGATT CCGGCTAGAGTGCAGTGATGTGATCTCGGCTCTCTGCAACCTCCGCCTCCTGTTTTCAAGTGATT T A ERI3 Ensembl:ENSG00000117419 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1016131087 Functional Loss SNV dbSNP153 33..33 33 - - - 31532 RMVar_ID_31532 Human_SNP_ID_11442809 A-to-I Human chr1 - 44234881 44234881 44234881 CTCTTAGGCCGGGTATGGTGGCACACGCGTGTAATCCCAGCTACTTGGGAGGCTGAGGCACGGGA CTCTTAGGCCGGGTATGGTGGCACACGCGTGTGATCCCAGCTACTTGGGAGGCTGAGGCACGGGA T C ERI3 Ensembl:ENSG00000117419 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1044127618 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11000244 31533 RMVar_ID_31533 Human_SNP_ID_11453290 A-to-I Human chr1 - 44281547 44281547 44281547 GTCTCACTCTGTCACCCAGGCTAGAATGCGGTAGTATAAACATGGCTCGCTGCAGCCTTGAACTC GTCTCACTCTGTCACCCAGGCTAGAATGCGGTCGTATAAACATGGCTCGCTGCAGCCTTGAACTC T G ERI3 Ensembl:ENSG00000117419 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973811618 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 31534 RMVar_ID_31534 Human_SNP_ID_11469828 A-to-I Human chr1 - 44352359 44352359 44352359 TTGCCCATGCTGGGCTCGAACTCCTGGGTTCAAGTGATCTCCTGCCCACAAGTAGCTGGAGCTAC TTGCCCATGCTGGGCTCGAACTCCTGGGTTCAGGTGATCTCCTGCCCACAAGTAGCTGGAGCTAC T C ERI3 Ensembl:ENSG00000117419 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs895306584 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1348767,Human_RBP_ID_5829460,Human_RBP_ID_19367909 RMVar_hsa_circ_280248,RMVar_hsa_circ_132378,RMVar_hsa_circ_132386,RMVar_hsa_circ_283715,RMVar_hsa_circ_132391,RMVar_hsa_circ_294339,RMVar_hsa_circ_368605,RMVar_hsa_circ_91831,RMVar_hsa_circ_132392,RMVar_hsa_circ_132393,RMVar_hsa_circ_300398,RMVar_hsa_circ_91331,RMVar_hsa_circ_132397,RMVar_hsa_circ_132398,RMVar_hsa_circ_285352,RMVar_hsa_circ_132400 31535 RMVar_ID_31535 Human_SNP_ID_11542636 A-to-I Human chr1 - 44661406 44661406 44661406 CAAACCCCCTTTTTTACTCTTAAAAAAAAAAAAAGAAAAAGAAAGCTGCACATGGTGGTGGGTGC CAAACCCCCTTTTTTACTCTTAAAAAAAAAAAGAGAAAAAGAAAGCTGCACATGGTGGTGGGTGC T C TMEM53 Ensembl:ENSG00000126106 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1010531434 Functional Loss SNV dbSNP153 33..33 33 - - - 31536 RMVar_ID_31536 Human_SNP_ID_11547161 A-to-I Human chr1 + 44681353 44681353 44681353 TTTAAGTTAGCCAGGCATGGTGGTGCACACCCATAGTCCTAGCTACTCAGGAGGCTGAGGCAGGA TTTAAGTTAGCCAGGCATGGTGGTGCACACCCGTAGTCCTAGCTACTCAGGAGGCTGAGGCAGGA A G ARMH1 Ensembl:ENSG00000198520 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs113988186 Functional Loss SNV dbSNP153 33..33 33 - - - 31537 RMVar_ID_31537 Human_SNP_ID_11564338 A-to-I Human chr1 + 44743693 44743693 44743693 TTGCGCCTGTGGTCCCAGCTACTCCAGAGGCTAAGGCAGGAGGATTGCTTGAGCCCAGGAGTTCA TTGCGCCTGTGGTCCCAGCTACTCCAGAGGCTGAGGCAGGAGGATTGCTTGAGCCCAGGAGTTCA A G KIF2C Ensembl:ENSG00000142945 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs942505403 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98107,RMVar_hsa_circ_115782,RMVar_hsa_circ_105535,RMVar_hsa_circ_132409,RMVar_hsa_circ_132410,RMVar_hsa_circ_132411 31538 RMVar_ID_31538 Human_SNP_ID_11564593 A-to-I Human chr1 + 44744697 44744697 44744697 CTGAAGCGGGCGGATCATGAGGTCAGGAGTTCAAGACCAGCCTGGCCAATATAGTGAACCTGCAT CTGAAGCGGGCGGATCATGAGGTCAGGAGTTCGAGACCAGCCTGGCCAATATAGTGAACCTGCAT A G KIF2C Ensembl:ENSG00000142945 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1330718234 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98107,RMVar_hsa_circ_115782,RMVar_hsa_circ_105535,RMVar_hsa_circ_132409,RMVar_hsa_circ_132410,RMVar_hsa_circ_132411 31539 RMVar_ID_31539 Human_SNP_ID_11564600 A-to-I Human chr1 + 44744717 44744717 44744717 GGTCAGGAGTTCAAGACCAGCCTGGCCAATATAGTGAACCTGCATCTCTACTAAAAATCCAAAAA GGTCAGGAGTTCAAGACCAGCCTGGCCAATATGGTGAACCTGCATCTCTACTAAAAATCCAAAAA A G KIF2C Ensembl:ENSG00000142945 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1368678527 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98107,RMVar_hsa_circ_115782,RMVar_hsa_circ_105535,RMVar_hsa_circ_132409,RMVar_hsa_circ_132410,RMVar_hsa_circ_132411 31540 RMVar_ID_31540 Human_SNP_ID_11565030 A-to-I Human chr1 + 44746152 44746152 44746152 CGCCCACCTCGGCCTCCCAAAGTGCTGGGGTTACAGGCGTGAGCCACCGCACCCAGTCCTGCAGG CGCCCACCTCGGCCTCCCAAAGTGCTGGGGTTGCAGGCGTGAGCCACCGCACCCAGTCCTGCAGG A G KIF2C Ensembl:ENSG00000142945 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1207486990 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98107,RMVar_hsa_circ_115782,RMVar_hsa_circ_105535,RMVar_hsa_circ_132409,RMVar_hsa_circ_132410,RMVar_hsa_circ_132411 31541 RMVar_ID_31541 Human_SNP_ID_11565236 A-to-I Human chr1 + 44746961 44746961 44746961 GCTCTGTTGCCCAGGCTGGAGGGCAGTGGCTCAATCTCAGCTCAATGCAACCTCCGCCTCCTGGA GCTCTGTTGCCCAGGCTGGAGGGCAGTGGCTCCATCTCAGCTCAATGCAACCTCCGCCTCCTGGA A C KIF2C Ensembl:ENSG00000142945 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1557590174 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98107,RMVar_hsa_circ_115782,RMVar_hsa_circ_105535,RMVar_hsa_circ_132409,RMVar_hsa_circ_132410,RMVar_hsa_circ_132411 31542 RMVar_ID_31542 Human_SNP_ID_11565239 A-to-I Human chr1 + 44746967 44746967 44746967 TTGCCCAGGCTGGAGGGCAGTGGCTCAATCTCAGCTCAATGCAACCTCCGCCTCCTGGATTCCAG TTGCCCAGGCTGGAGGGCAGTGGCTCAATCTCGGCTCAATGCAACCTCCGCCTCCTGGATTCCAG A G KIF2C Ensembl:ENSG00000142945 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1430607289 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98107,RMVar_hsa_circ_115782,RMVar_hsa_circ_105535,RMVar_hsa_circ_132409,RMVar_hsa_circ_132410,RMVar_hsa_circ_132411 31543 RMVar_ID_31543 Human_SNP_ID_11570141 A-to-I Human chr1 - 44764782 44764782 44764782 ATATACGACTGGGCGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGTCGGGGCGGGAGG ATATACGACTGGGCGTGGTGGCTCACGCCTGTCATCCCAGCACTTTGGGAGGTCGGGGCGGGAGG T G AL592166.1 Ensembl:ENSG00000225721 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1457846302 Functional Loss SNV dbSNP153 33..33 33 - - - 31544 RMVar_ID_31544 Human_SNP_ID_11573719 A-to-I Human chr1 + 44777189 44777189 44777189 CGCCTCCTGGGTTGAAGTGATTCTCCTGCCTCAGCCTCCCAAGAAGCTGGGATTACAGGCGTGTG CGCCTCCTGGGTTGAAGTGATTCTCCTGCCTCTGCCTCCCAAGAAGCTGGGATTACAGGCGTGTG A T RPS8 Ensembl:ENSG00000142937 Protein coding intron GSE38233;GSE107867 cultured B-cells;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 24183664,30559470 RNA-Seq:(High) rs1557609074 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557152 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_132430 31545 RMVar_ID_31545 Human_SNP_ID_11573761 A-to-I Human chr1 + 44777332 44777332 44777332 GCTTTAAGTGATCCACCCGCCTTGACCTCCCAAAGTGCTGGGGTTACGGGCGTGAGTCACCGTGC GCTTTAAGTGATCCACCCGCCTTGACCTCCCAGAGTGCTGGGGTTACGGGCGTGAGTCACCGTGC A G RPS8 Ensembl:ENSG00000142937 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs994479987 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557153,Human_RBP_ID_18576048 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_132430 31546 RMVar_ID_31546 Human_SNP_ID_11573992 A-to-I Human chr1 + 44778041 44778041 44778041 GAAGAAGAGATTTTAAACAAAAAACGATCTAAAAAAATTCAGAAGAAATATGATGAAAGGAAAAA GAAGAAGAGATTTTAAACAAAAAACGATCTAATAAAATTCAGAAGAAATATGATGAAAGGAAAAA A T RPS8 Ensembl:ENSG00000142937 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1453215486 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_356254,Human_RBP_ID_1748767,Human_RBP_ID_2149552,Human_RBP_ID_18524731,Human_RBP_ID_22875272,Human_RBP_ID_23397967,Human_RBP_ID_26865598,Human_RBP_ID_27183949 Human_Splice_Rec_62126,Human_Splice_Rec_62134,Human_Splice_Rec_62135,Human_Splice_Rec_62144,Human_Splice_Rec_62145,Human_Splice_Rec_62156,Human_Splice_Rec_62157,Human_Splice_Rec_62160,Human_Splice_Rec_62161,Human_Splice_Rec_62164,Human_Splice_Rec_62165 RMVar_hsa_circ_97389,RMVar_hsa_circ_117122,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_88034,RMVar_hsa_circ_132432,RMVar_hsa_circ_132431,RMVar_hsa_circ_132434 31547 RMVar_ID_31547 Human_SNP_ID_11587172 A-to-I Human chr1 + 44815832 44815832 44815832 GGGCTCAAGCAATGGTCCCACTCCGTCCTCCCAAAGTGCTGGGATTACAGGCATGAAGCACCACC GGGCTCAAGCAATGGTCCCACTCCGTCCTCCCGAAGTGCTGGGATTACAGGCATGAAGCACCACC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973184164 Functional Loss SNV dbSNP153 33..33 33 - - - 31548 RMVar_ID_31548 Human_SNP_ID_11587244 A-to-I Human chr1 + 44816132 44816132 44816132 GAGCTCAGGAGTTCGGGATCAGCCTGGGCAACATGGCAAAACCCTGTCTCTAAAATACAAAAAAC GAGCTCAGGAGTTCGGGATCAGCCTGGGCAACGTGGCAAAACCCTGTCTCTAAAATACAAAAAAC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928952965 Functional Loss SNV dbSNP153 33..33 33 - - - 31549 RMVar_ID_31549 Human_SNP_ID_11587928 A-to-I Human chr1 + 44817912 44817912 44817912 GAATCTGGGAGTTTGATACCAGTTCGGGCAACATGGCGAAATCCCGTCTCTACAAAAAATACAAA GAATCTGGGAGTTTGATACCAGTTCGGGCAACGTGGCGAAATCCCGTCTCTACAAAAAATACAAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1226925884 Functional Loss SNV dbSNP153 33..33 33 - - - 31550 RMVar_ID_31550 Human_SNP_ID_11600257 A-to-I Human chr1 - 44864440 44864440 44864440 CTCCCACCTCAGCCTTCCGAGTAGCTGGGACTACAGGCACACACCATCACGCCAGGCTAATTTTT CTCCCACCTCAGCCTTCCGAGTAGCTGGGACTGCAGGCACACACCATCACGCCAGGCTAATTTTT T C EIF2B3 Ensembl:ENSG00000070785 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1283309567 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26060,RMVar_hsa_circ_117887,RMVar_hsa_circ_334480,RMVar_hsa_circ_132444,RMVar_hsa_circ_353088,RMVar_hsa_circ_51083 31551 RMVar_ID_31551 Human_SNP_ID_11601443 A-to-I Human chr1 - 44869725 44869725 44869725 GTGGTGGCTCGCGCCTATAGTCCCAGATATTCAGGAGGCTGAGGCAGAAGAATCGCTTGAACCCG GTGGTGGCTCGCGCCTATAGTCCCAGATATTCGGGAGGCTGAGGCAGAAGAATCGCTTGAACCCG T C EIF2B3 Ensembl:ENSG00000070785 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs938316259 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26060,RMVar_hsa_circ_117887,RMVar_hsa_circ_334480,RMVar_hsa_circ_132444,RMVar_hsa_circ_353088,RMVar_hsa_circ_51083 31552 RMVar_ID_31552 Human_SNP_ID_11602070 A-to-I Human chr1 - 44872590 44872590 44872590 GCTGGAGTACAGTGGCATGATCATAGCTCACTACAACCTCAAACTCCTGAGCTCCAACAGTCCTC GCTGGAGTACAGTGGCATGATCATAGCTCACTGCAACCTCAAACTCCTGAGCTCCAACAGTCCTC T C EIF2B3 Ensembl:ENSG00000070785 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1280571719 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26060,RMVar_hsa_circ_117887,RMVar_hsa_circ_334480,RMVar_hsa_circ_132444,RMVar_hsa_circ_353088,RMVar_hsa_circ_51083 31553 RMVar_ID_31553 Human_SNP_ID_11606593 A-to-I Human chr1 - 44891947 44891947 44891947 ATGGGCTGAACTCAGGAGTTCCAGACCAGCCTAGGCAACATAGCAAGATGCCATCTCTACAAAAA ATGGGCTGAACTCAGGAGTTCCAGACCAGCCTGGGCAACATAGCAAGATGCCATCTCTACAAAAA T C EIF2B3 Ensembl:ENSG00000070785 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs890708385 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9029,RMVar_hsa_circ_117887,RMVar_hsa_circ_334480,RMVar_hsa_circ_132444,RMVar_hsa_circ_353088,RMVar_hsa_circ_81251,RMVar_hsa_circ_132446,RMVar_hsa_circ_132450,RMVar_hsa_circ_288360,RMVar_hsa_circ_62322,RMVar_hsa_circ_132452,RMVar_hsa_circ_320626,RMVar_hsa_circ_32987,RMVar_hsa_circ_132454,RMVar_hsa_circ_314574 31554 RMVar_ID_31554 Human_SNP_ID_11612889 A-to-I Human chr1 - 44920916 44920916 44920916 AGTAAAAAATAGAGCTACCATACAATCCAGCAATCCCACTCCTAGGTATATACCCACAAGAAAGG AGTAAAAAATAGAGCTACCATACAATCCAGCAGTCCCACTCCTAGGTATATACCCACAAGAAAGG T C EIF2B3 Ensembl:ENSG00000070785 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1433276392 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117887,RMVar_hsa_circ_132444,RMVar_hsa_circ_353088,RMVar_hsa_circ_81251,RMVar_hsa_circ_132446,RMVar_hsa_circ_62322,RMVar_hsa_circ_32987,RMVar_hsa_circ_25558,RMVar_hsa_circ_367462 31555 RMVar_ID_31555 Human_SNP_ID_11613131 A-to-I Human chr1 - 44922071 44922071 44922071 GAAACCCCATCTCTACTAAAAATACAAAAATTAGCTGAGCGTGGTTGTGGGCGCCTGTGATCCCA GAAACCCCATCTCTACTAAAAATACAAAAATTCGCTGAGCGTGGTTGTGGGCGCCTGTGATCCCA T G EIF2B3 Ensembl:ENSG00000070785 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs892233068 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117887,RMVar_hsa_circ_132444,RMVar_hsa_circ_353088,RMVar_hsa_circ_81251,RMVar_hsa_circ_132446,RMVar_hsa_circ_62322,RMVar_hsa_circ_32987,RMVar_hsa_circ_25558,RMVar_hsa_circ_367462 31556 RMVar_ID_31556 Human_SNP_ID_11616995 A-to-I Human chr1 - 44938917 44938917 44938917 TTTTGTATTTTTTGTAGGCACAGGGTTTCACAATGTTGCCCAGGCTGGCCTCGAACTCTTGAGCT TTTTGTATTTTTTGTAGGCACAGGGTTTCACAGTGTTGCCCAGGCTGGCCTCGAACTCTTGAGCT T C EIF2B3 Ensembl:ENSG00000070785 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1052010837 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81251,RMVar_hsa_circ_132446,RMVar_hsa_circ_32987,RMVar_hsa_circ_65768,RMVar_hsa_circ_25558,RMVar_hsa_circ_339191,RMVar_hsa_circ_362331,RMVar_hsa_circ_326035,RMVar_hsa_circ_132458,RMVar_hsa_circ_132457,RMVar_hsa_circ_355408 31557 RMVar_ID_31557 Human_SNP_ID_11626135 A-to-I Human chr1 - 44977629 44977629 44977629 AAGACCCTGTCTCTACTAAAAAGACAAAAATTAGCTGGGCATGGCGGTGCACATCTGTAATCCTA AAGACCCTGTCTCTACTAAAAAGACAAAAATTGGCTGGGCATGGCGGTGCACATCTGTAATCCTA T C EIF2B3 Ensembl:ENSG00000070785 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1247042437 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81251,RMVar_hsa_circ_132446,RMVar_hsa_circ_38352,RMVar_hsa_circ_65768,RMVar_hsa_circ_326035,RMVar_hsa_circ_132458,RMVar_hsa_circ_82339,RMVar_hsa_circ_132461,RMVar_hsa_circ_16912 31558 RMVar_ID_31558 Human_SNP_ID_61775087 A-to-I Human chr2 - 15353684 15353684 15353684 TTGCAGGTTATCCTAAAAGTTGGGATGTTTGTAGCCAGTTAGGACAATCAGAAGGTTACCAGGAC TTGCAGGTTATCCTAAAAGTTGGGATGTTTGTGGCCAGTTAGGACAATCAGAAGGTTACCAGGAC T C NBAS Ensembl:ENSG00000151779 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs559655377 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1297855 Human_Splice_Rec_219538,Human_Splice_Rec_219640 RMVar_hsa_circ_99036,RMVar_hsa_circ_98297,RMVar_hsa_circ_13892,RMVar_hsa_circ_91520,RMVar_hsa_circ_81905,RMVar_hsa_circ_197099,RMVar_hsa_circ_197101,RMVar_hsa_circ_197102,RMVar_hsa_circ_197100,RMVar_hsa_circ_53372,RMVar_hsa_circ_348898,RMVar_hsa_circ_25934,RMVar_hsa_circ_47665,RMVar_hsa_circ_115970,RMVar_hsa_circ_370539,RMVar_hsa_circ_375394,RMVar_hsa_circ_373688,RMVar_hsa_circ_118904,RMVar_hsa_circ_85879,RMVar_hsa_circ_110579,RMVar_hsa_circ_67773,RMVar_hsa_circ_197117,RMVar_hsa_circ_197119,RMVar_hsa_circ_197121,RMVar_hsa_circ_197122,RMVar_hsa_circ_197120,RMVar_hsa_circ_197118,RMVar_hsa_circ_197116,RMVar_hsa_circ_103039,RMVar_hsa_circ_20417,RMVar_hsa_circ_23390,RMVar_hsa_circ_27223,RMVar_hsa_circ_197129,RMVar_hsa_circ_369298,RMVar_hsa_circ_106857,RMVar_hsa_circ_29727,RMVar_hsa_circ_197131,RMVar_hsa_circ_10196,RMVar_hsa_circ_197130,RMVar_hsa_circ_371165,RMVar_hsa_circ_375423,RMVar_hsa_circ_329776,RMVar_hsa_circ_50779,RMVar_hsa_circ_2150,RMVar_hsa_circ_127524,RMVar_hsa_circ_86333,RMVar_hsa_circ_92281,RMVar_hsa_circ_197133,RMVar_hsa_circ_197134,RMVar_hsa_circ_269635,RMVar_hsa_circ_95969,RMVar_hsa_circ_32934,RMVar_hsa_circ_52084,RMVar_hsa_circ_197143,RMVar_hsa_circ_197144,RMVar_hsa_circ_102634,RMVar_hsa_circ_310127,RMVar_hsa_circ_106681,RMVar_hsa_circ_102570,RMVar_hsa_circ_5744,RMVar_hsa_circ_46124,RMVar_hsa_circ_15779,RMVar_hsa_circ_197146,RMVar_hsa_circ_197148,RMVar_hsa_circ_197149,RMVar_hsa_circ_197147,RMVar_hsa_circ_329709,RMVar_hsa_circ_197145,RMVar_hsa_circ_339771,RMVar_hsa_circ_315554,RMVar_hsa_circ_271477,RMVar_hsa_circ_268469,RMVar_hsa_circ_3469,RMVar_hsa_circ_9233,RMVar_hsa_circ_11286,RMVar_hsa_circ_197154,RMVar_hsa_circ_197155,RMVar_hsa_circ_197156,RMVar_hsa_circ_197153,RMVar_hsa_circ_317155,RMVar_hsa_circ_335500,RMVar_hsa_circ_339108,RMVar_hsa_circ_318232,RMVar_hsa_circ_312761,RMVar_hsa_circ_80633,RMVar_hsa_circ_103114,RMVar_hsa_circ_26001,RMVar_hsa_circ_197164,RMVar_hsa_circ_197157,RMVar_hsa_circ_197159,RMVar_hsa_circ_197160,RMVar_hsa_circ_197158,RMVar_hsa_circ_268872,RMVar_hsa_circ_373988,RMVar_hsa_circ_119257,RMVar_hsa_circ_87058,RMVar_hsa_circ_197162,RMVar_hsa_circ_197163,RMVar_hsa_circ_126959,RMVar_hsa_circ_197165,RMVar_hsa_circ_75290,RMVar_hsa_circ_302412,RMVar_hsa_circ_326756,RMVar_hsa_circ_327025,RMVar_hsa_circ_330474,RMVar_hsa_circ_326930,RMVar_hsa_circ_304673,RMVar_hsa_circ_296502,RMVar_hsa_circ_300206,RMVar_hsa_circ_281049,RMVar_hsa_circ_197167,RMVar_hsa_circ_197168,RMVar_hsa_circ_197166 31559 RMVar_ID_31559 Human_SNP_ID_61811834 A-to-I Human chr2 - 15501900 15501900 15501900 CTCTTAGCCTGGCGTGGTGGCTTACACCTGTTATCCCAGTTCTTTGGGAGGCTGAGGTGGGAGGA CTCTTAGCCTGGCGTGGTGGCTTACACCTGTTTTCCCAGTTCTTTGGGAGGCTGAGGTGGGAGGA T A NBAS Ensembl:ENSG00000151779 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1327533066 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98297,RMVar_hsa_circ_197099,RMVar_hsa_circ_348898,RMVar_hsa_circ_47665,RMVar_hsa_circ_85879,RMVar_hsa_circ_110579,RMVar_hsa_circ_197121,RMVar_hsa_circ_197122,RMVar_hsa_circ_103039,RMVar_hsa_circ_20417,RMVar_hsa_circ_197129,RMVar_hsa_circ_197186,RMVar_hsa_circ_127524,RMVar_hsa_circ_102570,RMVar_hsa_circ_5744,RMVar_hsa_circ_197145,RMVar_hsa_circ_315554,RMVar_hsa_circ_197155,RMVar_hsa_circ_197156,RMVar_hsa_circ_339108,RMVar_hsa_circ_80633,RMVar_hsa_circ_103114,RMVar_hsa_circ_197157,RMVar_hsa_circ_197158,RMVar_hsa_circ_87058,RMVar_hsa_circ_197165,RMVar_hsa_circ_300206,RMVar_hsa_circ_348586,RMVar_hsa_circ_79073,RMVar_hsa_circ_197171,RMVar_hsa_circ_351660,RMVar_hsa_circ_325475,RMVar_hsa_circ_297533,RMVar_hsa_circ_62183,RMVar_hsa_circ_5971,RMVar_hsa_circ_197181,RMVar_hsa_circ_83578,RMVar_hsa_circ_277409,RMVar_hsa_circ_372509,RMVar_hsa_circ_43122,RMVar_hsa_circ_197187,RMVar_hsa_circ_55454,RMVar_hsa_circ_197185,RMVar_hsa_circ_324671,RMVar_hsa_circ_197198,RMVar_hsa_circ_356180,RMVar_hsa_circ_330690,RMVar_hsa_circ_273263,RMVar_hsa_circ_197201,RMVar_hsa_circ_294506,RMVar_hsa_circ_197210,RMVar_hsa_circ_119428,RMVar_hsa_circ_276384,RMVar_hsa_circ_295556,RMVar_hsa_circ_303501,RMVar_hsa_circ_197211,RMVar_hsa_circ_324973,RMVar_hsa_circ_299133,RMVar_hsa_circ_125017,RMVar_hsa_circ_273209,RMVar_hsa_circ_197214,RMVar_hsa_circ_197216,RMVar_hsa_circ_197217,RMVar_hsa_circ_197215,RMVar_hsa_circ_197212,RMVar_hsa_circ_197213,RMVar_hsa_circ_297618,RMVar_hsa_circ_94047,RMVar_hsa_circ_115853,RMVar_hsa_circ_197227,RMVar_hsa_circ_265672,RMVar_hsa_circ_65754,RMVar_hsa_circ_79369,RMVar_hsa_circ_197228,RMVar_hsa_circ_197229,RMVar_hsa_circ_334540,RMVar_hsa_circ_197231,RMVar_hsa_circ_5103,RMVar_hsa_circ_376957,RMVar_hsa_circ_38043,RMVar_hsa_circ_197232,RMVar_hsa_circ_370488,RMVar_hsa_circ_353907,RMVar_hsa_circ_313196,RMVar_hsa_circ_197240,RMVar_hsa_circ_197233,RMVar_hsa_circ_197235,RMVar_hsa_circ_197236,RMVar_hsa_circ_197234,RMVar_hsa_circ_336307,RMVar_hsa_circ_367655,RMVar_hsa_circ_10162,RMVar_hsa_circ_284924,RMVar_hsa_circ_296509,RMVar_hsa_circ_337926,RMVar_hsa_circ_361206,RMVar_hsa_circ_328834,RMVar_hsa_circ_288829,RMVar_hsa_circ_197238,RMVar_hsa_circ_197239,RMVar_hsa_circ_197237 31560 RMVar_ID_31560 Human_SNP_ID_61816015 A-to-I Human chr2 - 15519717 15519717 15519717 TTCTTGGCTGCATACAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGAAGG TTCTTGGCTGCATACAGTGGCTCATGCCTGTAGTCCCAGCACTTTGGGAGGCCAAGGCAGGAAGG T C NBAS Ensembl:ENSG00000151779 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1425245581 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_749,RMVar_hsa_circ_98297,RMVar_hsa_circ_197099,RMVar_hsa_circ_85879,RMVar_hsa_circ_110579,RMVar_hsa_circ_197121,RMVar_hsa_circ_197122,RMVar_hsa_circ_103039,RMVar_hsa_circ_20417,RMVar_hsa_circ_197129,RMVar_hsa_circ_197186,RMVar_hsa_circ_127524,RMVar_hsa_circ_197156,RMVar_hsa_circ_80633,RMVar_hsa_circ_103114,RMVar_hsa_circ_197157,RMVar_hsa_circ_197158,RMVar_hsa_circ_79073,RMVar_hsa_circ_197171,RMVar_hsa_circ_351660,RMVar_hsa_circ_325475,RMVar_hsa_circ_83578,RMVar_hsa_circ_372509,RMVar_hsa_circ_43122,RMVar_hsa_circ_197185,RMVar_hsa_circ_356180,RMVar_hsa_circ_330690,RMVar_hsa_circ_119428,RMVar_hsa_circ_295556,RMVar_hsa_circ_197211,RMVar_hsa_circ_324973,RMVar_hsa_circ_299133,RMVar_hsa_circ_125017,RMVar_hsa_circ_273209,RMVar_hsa_circ_197214,RMVar_hsa_circ_197215,RMVar_hsa_circ_197212,RMVar_hsa_circ_197213,RMVar_hsa_circ_94047,RMVar_hsa_circ_115853,RMVar_hsa_circ_265672,RMVar_hsa_circ_65754,RMVar_hsa_circ_197228,RMVar_hsa_circ_197231,RMVar_hsa_circ_376957,RMVar_hsa_circ_197232,RMVar_hsa_circ_370488,RMVar_hsa_circ_353907,RMVar_hsa_circ_313196,RMVar_hsa_circ_197233,RMVar_hsa_circ_197235,RMVar_hsa_circ_197236,RMVar_hsa_circ_197234,RMVar_hsa_circ_336307,RMVar_hsa_circ_367655,RMVar_hsa_circ_284924,RMVar_hsa_circ_296509,RMVar_hsa_circ_337926,RMVar_hsa_circ_361206,RMVar_hsa_circ_81931,RMVar_hsa_circ_348417,RMVar_hsa_circ_197238,RMVar_hsa_circ_197239,RMVar_hsa_circ_197237,RMVar_hsa_circ_349360,RMVar_hsa_circ_278764,RMVar_hsa_circ_303616,RMVar_hsa_circ_197243,RMVar_hsa_circ_197244,RMVar_hsa_circ_197245,RMVar_hsa_circ_197242,RMVar_hsa_circ_308443,RMVar_hsa_circ_357294,RMVar_hsa_circ_96613,RMVar_hsa_circ_197246,RMVar_hsa_circ_197247 31561 RMVar_ID_31561 Human_SNP_ID_61816016 A-to-I Human chr2 - 15519718 15519718 15519718 ATTCTTGGCTGCATACAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGAAG ATTCTTGGCTGCATACAGTGGCTCATGCCTGTGATCCCAGCACTTTGGGAGGCCAAGGCAGGAAG T C NBAS Ensembl:ENSG00000151779 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1033812644 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_749,RMVar_hsa_circ_98297,RMVar_hsa_circ_197099,RMVar_hsa_circ_85879,RMVar_hsa_circ_110579,RMVar_hsa_circ_197121,RMVar_hsa_circ_197122,RMVar_hsa_circ_103039,RMVar_hsa_circ_20417,RMVar_hsa_circ_197129,RMVar_hsa_circ_197186,RMVar_hsa_circ_127524,RMVar_hsa_circ_197156,RMVar_hsa_circ_80633,RMVar_hsa_circ_103114,RMVar_hsa_circ_197157,RMVar_hsa_circ_197158,RMVar_hsa_circ_79073,RMVar_hsa_circ_197171,RMVar_hsa_circ_351660,RMVar_hsa_circ_325475,RMVar_hsa_circ_83578,RMVar_hsa_circ_372509,RMVar_hsa_circ_43122,RMVar_hsa_circ_197185,RMVar_hsa_circ_356180,RMVar_hsa_circ_330690,RMVar_hsa_circ_119428,RMVar_hsa_circ_295556,RMVar_hsa_circ_197211,RMVar_hsa_circ_324973,RMVar_hsa_circ_299133,RMVar_hsa_circ_125017,RMVar_hsa_circ_273209,RMVar_hsa_circ_197214,RMVar_hsa_circ_197215,RMVar_hsa_circ_197212,RMVar_hsa_circ_197213,RMVar_hsa_circ_94047,RMVar_hsa_circ_115853,RMVar_hsa_circ_265672,RMVar_hsa_circ_65754,RMVar_hsa_circ_197228,RMVar_hsa_circ_197231,RMVar_hsa_circ_376957,RMVar_hsa_circ_197232,RMVar_hsa_circ_370488,RMVar_hsa_circ_353907,RMVar_hsa_circ_313196,RMVar_hsa_circ_197233,RMVar_hsa_circ_197235,RMVar_hsa_circ_197236,RMVar_hsa_circ_197234,RMVar_hsa_circ_336307,RMVar_hsa_circ_367655,RMVar_hsa_circ_284924,RMVar_hsa_circ_296509,RMVar_hsa_circ_337926,RMVar_hsa_circ_361206,RMVar_hsa_circ_81931,RMVar_hsa_circ_348417,RMVar_hsa_circ_197238,RMVar_hsa_circ_197239,RMVar_hsa_circ_197237,RMVar_hsa_circ_349360,RMVar_hsa_circ_278764,RMVar_hsa_circ_303616,RMVar_hsa_circ_197243,RMVar_hsa_circ_197244,RMVar_hsa_circ_197245,RMVar_hsa_circ_197242,RMVar_hsa_circ_308443,RMVar_hsa_circ_357294,RMVar_hsa_circ_96613,RMVar_hsa_circ_197246,RMVar_hsa_circ_197247 31562 RMVar_ID_31562 Human_SNP_ID_61837769 A-to-I Human chr2 + 15607744 15607744 15607744 GGACTGCAGGCACATGCCACCTTAGTAGAGATAGGGTTTCACTATGTTGCTTAGGCTAGTCTCAA GGACTGCAGGCACATGCCACCTTAGTAGAGATGGGGTTTCACTATGTTGCTTAGGCTAGTCTCAA A G DDX1 Ensembl:ENSG00000079785 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1021545786 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108007,RMVar_hsa_circ_361109,RMVar_hsa_circ_111073,RMVar_hsa_circ_76143,RMVar_hsa_circ_85320,RMVar_hsa_circ_4017,RMVar_hsa_circ_98788,RMVar_hsa_circ_197260,RMVar_hsa_circ_197262,RMVar_hsa_circ_197261,RMVar_hsa_circ_124948,RMVar_hsa_circ_197259,RMVar_hsa_circ_197265,RMVar_hsa_circ_23533,RMVar_hsa_circ_62309,RMVar_hsa_circ_63311,RMVar_hsa_circ_121495,RMVar_hsa_circ_197266,RMVar_hsa_circ_197267,RMVar_hsa_circ_50973,RMVar_hsa_circ_14803,RMVar_hsa_circ_89474,RMVar_hsa_circ_365573,RMVar_hsa_circ_197270,RMVar_hsa_circ_322506,RMVar_hsa_circ_197271 31563 RMVar_ID_31563 Human_SNP_ID_62333016 A-to-I Human chr2 + 17618220 17618220 17618220 AAACTGATGGCTTAAAACAACACAAATGTATTATCTTACACTTTTGGGGGCCAGAAATCTGAAAC AAACTGATGGCTTAAAACAACACAAATGTATTGTCTTACACTTTTGGGGGCCAGAAATCTGAAAC A G VSNL1 Ensembl:ENSG00000163032 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1261941494 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9098428 31564 RMVar_ID_31564 Human_SNP_ID_62343813 A-to-I Human chr2 - 17665523 17665523 17665523 CAAACTACATTGCCTTTCAGACCTGTGACTCAAGAAGAAGATGATGACCAAAGGTGATTTGTAAC CAAACTACATTGCCTTTCAGACCTGTGACTCAGGAAGAAGATGATGACCAAAGGTGATTTGTAAC T C SMC6 Ensembl:ENSG00000163029 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs771914831 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_61564,Human_RBP_ID_539183,Human_RBP_ID_1021047,Human_RBP_ID_1904219,Human_RBP_ID_8843777,Human_RBP_ID_13698062,Human_RBP_ID_22504780 Human_Splice_Rec_220294,Human_Splice_Rec_220346,Human_Splice_Rec_220352,Human_Splice_Rec_220410 RMVar_hsa_circ_197278,RMVar_hsa_circ_197280,RMVar_hsa_circ_197279 31565 RMVar_ID_31565 Human_SNP_ID_62358980 A-to-I Human chr2 - 17728806 17728806 17728806 AGGCAGAGGTTGCAGTGAGCTGAGATCACGCCACTGCACTCCAGCCTGGGTGACACAGCGAGACC AGGCAGAGGTTGCAGTGAGCTGAGATCACGCCTCTGCACTCCAGCCTGGGTGACACAGCGAGACC T A SMC6 Ensembl:ENSG00000163029 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs953869247 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_197280,RMVar_hsa_circ_197279,RMVar_hsa_circ_347402,RMVar_hsa_circ_58792,RMVar_hsa_circ_344097,RMVar_hsa_circ_56685,RMVar_hsa_circ_358649,RMVar_hsa_circ_284397,RMVar_hsa_circ_7227,RMVar_hsa_circ_351792,RMVar_hsa_circ_69531,RMVar_hsa_circ_356137,RMVar_hsa_circ_358650,RMVar_hsa_circ_46278,RMVar_hsa_circ_290791,RMVar_hsa_circ_346764,RMVar_hsa_circ_197284,RMVar_hsa_circ_275701,RMVar_hsa_circ_24864,RMVar_hsa_circ_197285,RMVar_hsa_circ_73086,RMVar_hsa_circ_60434,RMVar_hsa_circ_66630,RMVar_hsa_circ_350840,RMVar_hsa_circ_21220,RMVar_hsa_circ_353750,RMVar_hsa_circ_355833,RMVar_hsa_circ_300149,RMVar_hsa_circ_197289,RMVar_hsa_circ_75003,RMVar_hsa_circ_327019,RMVar_hsa_circ_197290 31566 RMVar_ID_31566 Human_SNP_ID_62360744 A-to-I Human chr2 - 17735957 17735957 17735957 TGCCTGAAGAATGGTTGTCAGTGTGGTCCAGCACAAGTTTGAGGTAGTTCTAAGGACTCTATCCC TGCCTGAAGAATGGTTGTCAGTGTGGTCCAGCGCAAGTTTGAGGTAGTTCTAAGGACTCTATCCC T C SMC6 Ensembl:ENSG00000163029 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs550415620 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13699136 RMVar_hsa_circ_197280,RMVar_hsa_circ_197279,RMVar_hsa_circ_347402,RMVar_hsa_circ_58792,RMVar_hsa_circ_344097,RMVar_hsa_circ_56685,RMVar_hsa_circ_358649,RMVar_hsa_circ_284397,RMVar_hsa_circ_7227,RMVar_hsa_circ_351792,RMVar_hsa_circ_69531,RMVar_hsa_circ_356137,RMVar_hsa_circ_358650,RMVar_hsa_circ_46278,RMVar_hsa_circ_346764,RMVar_hsa_circ_275701,RMVar_hsa_circ_24864,RMVar_hsa_circ_197285,RMVar_hsa_circ_73086,RMVar_hsa_circ_60434,RMVar_hsa_circ_66630,RMVar_hsa_circ_350840,RMVar_hsa_circ_21220,RMVar_hsa_circ_355833,RMVar_hsa_circ_300149,RMVar_hsa_circ_197289,RMVar_hsa_circ_75003,RMVar_hsa_circ_197292,RMVar_hsa_circ_308857,RMVar_hsa_circ_327019,RMVar_hsa_circ_197290,RMVar_hsa_circ_298596,RMVar_hsa_circ_325253 31567 RMVar_ID_31567 Human_SNP_ID_62360745 A-to-I Human chr2 - 17735957 17735957 17735957 TGCCTGAAGAATGGTTGTCAGTGTGGTCCAGCACAAGTTTGAGGTAGTTCTAAGGACTCTATCCC TGCCTGAAGAATGGTTGTCAGTGTGGTCCAGCCCAAGTTTGAGGTAGTTCTAAGGACTCTATCCC T G SMC6 Ensembl:ENSG00000163029 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs550415620 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13699136 RMVar_hsa_circ_197280,RMVar_hsa_circ_197279,RMVar_hsa_circ_347402,RMVar_hsa_circ_58792,RMVar_hsa_circ_344097,RMVar_hsa_circ_56685,RMVar_hsa_circ_358649,RMVar_hsa_circ_284397,RMVar_hsa_circ_7227,RMVar_hsa_circ_351792,RMVar_hsa_circ_69531,RMVar_hsa_circ_356137,RMVar_hsa_circ_358650,RMVar_hsa_circ_46278,RMVar_hsa_circ_346764,RMVar_hsa_circ_275701,RMVar_hsa_circ_24864,RMVar_hsa_circ_197285,RMVar_hsa_circ_73086,RMVar_hsa_circ_60434,RMVar_hsa_circ_66630,RMVar_hsa_circ_350840,RMVar_hsa_circ_21220,RMVar_hsa_circ_355833,RMVar_hsa_circ_300149,RMVar_hsa_circ_197289,RMVar_hsa_circ_75003,RMVar_hsa_circ_197292,RMVar_hsa_circ_308857,RMVar_hsa_circ_327019,RMVar_hsa_circ_197290,RMVar_hsa_circ_298596,RMVar_hsa_circ_325253 31568 RMVar_ID_31568 Human_SNP_ID_62889200 A-to-I Human chr2 + 19882016 19882016 19882016 CAAGATCCCCAAAGTGAGGACCTGATATGGTTAGGCTGTGTCCCCACCCAAAATCTCATCTTGAA CAAGATCCCCAAAGTGAGGACCTGATATGGTTTGGCTGTGTCCCCACCCAAAATCTCATCTTGAA A T LINC00954 Ensembl:ENSG00000228784 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1255563640 Functional Loss SNV dbSNP153 33..33 33 - - - 31569 RMVar_ID_31569 Human_SNP_ID_62924528 A-to-I Human chr2 + 20033282 20033281 20033283 CACGGCCATTTCATAGGTTGGCAAAACGTACTAAAGAGAGAAAAAAAATTGTATCAGATTTAATT CACGGCCATTTCATAGGTTGGCAAAACGTACT__AGAGAGAAAAAAAATTGTATCAGATTTAATT TAA T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs760502673 Functional Loss DEL dbSNP153 33..34 33 - - - 31570 RMVar_ID_31570 Human_SNP_ID_62924528 A-to-I Human chr2 + 20033283 20033281 20033283 ACGGCCATTTCATAGGTTGGCAAAACGTACTAAAGAGAGAAAAAAAATTGTATCAGATTTAATTC ACGGCCATTTCATAGGTTGGCAAAACGTACT__AGAGAGAAAAAAAATTGTATCAGATTTAATTC TAA T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs760502673 Functional Loss DEL dbSNP153 32..33 33 - - - 31571 RMVar_ID_31571 Human_SNP_ID_62924529 A-to-I Human chr2 + 20033283 20033281 20033283 ACGGCCATTTCATAGGTTGGCAAAACGTACTAAAGAGAGAAAAAAAATTGTATCAGATTTAATTC ACGGCCATTTCATAGGTTGGCAAAACGTACTA_AGAGAGAAAAAAAATTGTATCAGATTTAATTC TAA TA - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs760502673 Functional Loss DEL dbSNP153 33..33 33 - - - 31572 RMVar_ID_31572 Human_SNP_ID_62924530 A-to-I Human chr2 + 20033282 20033282 20033282 CACGGCCATTTCATAGGTTGGCAAAACGTACTAAAGAGAGAAAAAAAATTGTATCAGATTTAATT CACGGCCATTTCATAGGTTGGCAAAACGTACTGAAGAGAGAAAAAAAATTGTATCAGATTTAATT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878986489 Functional Loss SNV dbSNP153 33..33 33 - - - 31573 RMVar_ID_31573 Human_SNP_ID_62925963 A-to-I Human chr2 - 20039054 20039054 20039054 AAATTAGCTGGGCTTGGTGGCGCAGGCCTGCAATCCTAGCTACTCTGGAGGCTGAGGCAAAAGAA AAATTAGCTGGGCTTGGTGGCGCAGGCCTGCAGTCCTAGCTACTCTGGAGGCTGAGGCAAAAGAA T C LAPTM4A Ensembl:ENSG00000068697 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1236401739 Functional Loss SNV dbSNP153 33..33 33 - - - 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 31574 RMVar_ID_31574 Human_SNP_ID_62925974 A-to-I Human chr2 - 20039090 20039090 20039090 TAACATGGTGAAATCCTGTCTCTATTAAAAATACAAAAATTAGCTGGGCTTGGTGGCGCAGGCCT TAACATGGTGAAATCCTGTCTCTATTAAAAATGCAAAAATTAGCTGGGCTTGGTGGCGCAGGCCT T C LAPTM4A Ensembl:ENSG00000068697 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1387184870 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13739050 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 31575 RMVar_ID_31575 Human_SNP_ID_62966571 A-to-I Human chr2 - 20202778 20202778 20202778 GGGGCCTACCAGAAGCCCACCAAACAGGAGGAATTCTATGCCTGACGCGGGAGCCATGCGCCCCC GGGGCCTACCAGAAGCCCACCAAACAGGAGGACTTCTATGCCTGACGCGGGAGCCATGCGCCCCC T G SDC1 Ensembl:ENSG00000115884 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1472915386 Functional Loss SNV dbSNP153 33..33 33 - - - 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 31576 RMVar_ID_31576 Human_SNP_ID_62979427 A-to-I Human chr2 - 20251058 20251053 20251058 GCATAAATATTATTAATATTTTAAAAAGAGTTAAGTTGTATTTTGATAATTCACAAACTATCATG GCATAAATATTATTAATATTTTAAAAAGAGTT_____GTATTTTGATAATTCACAAACTATCATG CAACTT C PUM2 Ensembl:ENSG00000055917 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1174513585 Functional Loss DEL dbSNP153 33..37 33 - - - Human_RBP_ID_2616044 Human_miRNA_ID_1033524 31577 RMVar_ID_31577 Human_SNP_ID_62979428 A-to-I Human chr2 - 20251058 20251056 20251058 GCATAAATATTATTAATATTTTAAAAAGAGTTAAGTTGTATTTTGATAATTCACAAACTATCATG GCATAAATATTATTAATATTTTAAAAAGAGTT__GTTGTATTTTGATAATTCACAAACTATCATG CTT C PUM2 Ensembl:ENSG00000055917 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1374554090 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_2616044 Human_miRNA_ID_1033524 31578 RMVar_ID_31578 Human_SNP_ID_62979781 A-to-I Human chr2 - 20252342 20252342 20252342 CAGTGGTGTAATCTCGGCTAACTCTAGCCTCAACTTCCTGGCTCAAGCCATCCTCCCACTTTAGT CAGTGGTGTAATCTCGGCTAACTCTAGCCTCAGCTTCCTGGCTCAAGCCATCCTCCCACTTTAGT T C PUM2 Ensembl:ENSG00000055917 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1463927652 Functional Loss SNV dbSNP153 33..33 33 - - - 31579 RMVar_ID_31579 Human_SNP_ID_62982620 A-to-I Human chr2 - 20262475 20262475 20262475 AAAGAGTGTACCTATGCAAACCTAGATGGCATAGCCTACTACACACCTACTCTGTATATTGCGCC AAAGAGTGTACCTATGCAAACCTAGATGGCATGGCCTACTACACACCTACTCTGTATATTGCGCC T C PUM2 Ensembl:ENSG00000055917 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs532197366 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29978,RMVar_hsa_circ_126586,RMVar_hsa_circ_78595,RMVar_hsa_circ_289179,RMVar_hsa_circ_334160,RMVar_hsa_circ_45098,RMVar_hsa_circ_197337,RMVar_hsa_circ_375893,RMVar_hsa_circ_340658,RMVar_hsa_circ_197339,RMVar_hsa_circ_110711,RMVar_hsa_circ_197340,RMVar_hsa_circ_197338,RMVar_hsa_circ_40888,RMVar_hsa_circ_48130,RMVar_hsa_circ_39090,RMVar_hsa_circ_50340,RMVar_hsa_circ_87928,RMVar_hsa_circ_197346,RMVar_hsa_circ_197345,RMVar_hsa_circ_372212,RMVar_hsa_circ_65107,RMVar_hsa_circ_3749 31580 RMVar_ID_31580 Human_SNP_ID_62983830 A-to-I Human chr2 - 20266199 20266199 20266199 ACCTCGAGCTATGTGCCTTCCTCAGCCTCCCAAAAATGCTGGGATTATAGGCGTGAGCCACCGCG ACCTCGAGCTATGTGCCTTCCTCAGCCTCCCAGAAATGCTGGGATTATAGGCGTGAGCCACCGCG T C PUM2 Ensembl:ENSG00000055917 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1297221074 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14013844,Human_RBP_ID_18753113,Human_RBP_ID_25502987 RMVar_hsa_circ_29978,RMVar_hsa_circ_126586,RMVar_hsa_circ_78595,RMVar_hsa_circ_334160,RMVar_hsa_circ_45098,RMVar_hsa_circ_197337,RMVar_hsa_circ_375893,RMVar_hsa_circ_197339,RMVar_hsa_circ_110711,RMVar_hsa_circ_197340,RMVar_hsa_circ_197338,RMVar_hsa_circ_40888,RMVar_hsa_circ_48130,RMVar_hsa_circ_39090,RMVar_hsa_circ_50340,RMVar_hsa_circ_87928,RMVar_hsa_circ_197346,RMVar_hsa_circ_197345,RMVar_hsa_circ_372212,RMVar_hsa_circ_65107,RMVar_hsa_circ_197348,RMVar_hsa_circ_373409,RMVar_hsa_circ_330358,RMVar_hsa_circ_197347 31581 RMVar_ID_31581 Human_SNP_ID_62983891 A-to-I Human chr2 - 20266398 20266398 20266398 CTCTGTTGTCCAGGCTGGAGTGCAGTGGCACAATCTCATCTCATTGCAACCTCTGCCTCCCAGGC CTCTGTTGTCCAGGCTGGAGTGCAGTGGCACAGTCTCATCTCATTGCAACCTCTGCCTCCCAGGC T C PUM2 Ensembl:ENSG00000055917 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs958547507 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29978,RMVar_hsa_circ_126586,RMVar_hsa_circ_78595,RMVar_hsa_circ_334160,RMVar_hsa_circ_45098,RMVar_hsa_circ_197337,RMVar_hsa_circ_375893,RMVar_hsa_circ_197339,RMVar_hsa_circ_110711,RMVar_hsa_circ_197340,RMVar_hsa_circ_197338,RMVar_hsa_circ_40888,RMVar_hsa_circ_48130,RMVar_hsa_circ_39090,RMVar_hsa_circ_50340,RMVar_hsa_circ_87928,RMVar_hsa_circ_197346,RMVar_hsa_circ_197345,RMVar_hsa_circ_372212,RMVar_hsa_circ_65107,RMVar_hsa_circ_197348,RMVar_hsa_circ_373409,RMVar_hsa_circ_330358,RMVar_hsa_circ_197347 31582 RMVar_ID_31582 Human_SNP_ID_62984513 A-to-I Human chr2 - 20268561 20268561 20268561 CAAGCTAGAGTGCAGTGGTGCAGTCTCTGCTCACTGTAACCTTCGCCTCCTGGGTTCAAGCAATT CAAGCTAGAGTGCAGTGGTGCAGTCTCTGCTCGCTGTAACCTTCGCCTCCTGGGTTCAAGCAATT T C PUM2 Ensembl:ENSG00000055917 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs771093546 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29978,RMVar_hsa_circ_126586,RMVar_hsa_circ_78595,RMVar_hsa_circ_334160,RMVar_hsa_circ_45098,RMVar_hsa_circ_197337,RMVar_hsa_circ_375893,RMVar_hsa_circ_197339,RMVar_hsa_circ_110711,RMVar_hsa_circ_197340,RMVar_hsa_circ_197338,RMVar_hsa_circ_40888,RMVar_hsa_circ_48130,RMVar_hsa_circ_39090,RMVar_hsa_circ_50340,RMVar_hsa_circ_87928,RMVar_hsa_circ_197346,RMVar_hsa_circ_197345,RMVar_hsa_circ_372212,RMVar_hsa_circ_65107,RMVar_hsa_circ_197348,RMVar_hsa_circ_373409,RMVar_hsa_circ_330358,RMVar_hsa_circ_197347 31583 RMVar_ID_31583 Human_SNP_ID_62984523 A-to-I Human chr2 - 20268599 20268599 20268599 TTGTTTTGTTTGTTTAGACAGGGTCTTGCTCTATTGCCCAAGCTAGAGTGCAGTGGTGCAGTCTC TTGTTTTGTTTGTTTAGACAGGGTCTTGCTCTGTTGCCCAAGCTAGAGTGCAGTGGTGCAGTCTC T C PUM2 Ensembl:ENSG00000055917 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs996885867 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6971639,Human_RBP_ID_14013854 RMVar_hsa_circ_29978,RMVar_hsa_circ_126586,RMVar_hsa_circ_78595,RMVar_hsa_circ_334160,RMVar_hsa_circ_45098,RMVar_hsa_circ_197337,RMVar_hsa_circ_375893,RMVar_hsa_circ_197339,RMVar_hsa_circ_110711,RMVar_hsa_circ_197340,RMVar_hsa_circ_197338,RMVar_hsa_circ_40888,RMVar_hsa_circ_48130,RMVar_hsa_circ_39090,RMVar_hsa_circ_50340,RMVar_hsa_circ_87928,RMVar_hsa_circ_197346,RMVar_hsa_circ_197345,RMVar_hsa_circ_372212,RMVar_hsa_circ_65107,RMVar_hsa_circ_197348,RMVar_hsa_circ_373409,RMVar_hsa_circ_330358,RMVar_hsa_circ_197347 31584 RMVar_ID_31584 Human_SNP_ID_62985246 A-to-I Human chr2 - 20271484 20271484 20271484 TGTGGCGAAACCCCGTCTCTATTAAAAATACAAAAATTAGCCGGGTGCGGTGACATGTGCCTGTA TGTGGCGAAACCCCGTCTCTATTAAAAATACAGAAATTAGCCGGGTGCGGTGACATGTGCCTGTA T C PUM2 Ensembl:ENSG00000055917 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1450774180 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569434,Human_RBP_ID_25584819 RMVar_hsa_circ_29978,RMVar_hsa_circ_126586,RMVar_hsa_circ_78595,RMVar_hsa_circ_334160,RMVar_hsa_circ_45098,RMVar_hsa_circ_197337,RMVar_hsa_circ_375893,RMVar_hsa_circ_197339,RMVar_hsa_circ_110711,RMVar_hsa_circ_197340,RMVar_hsa_circ_197338,RMVar_hsa_circ_40888,RMVar_hsa_circ_48130,RMVar_hsa_circ_39090,RMVar_hsa_circ_50340,RMVar_hsa_circ_87928,RMVar_hsa_circ_197346,RMVar_hsa_circ_197345,RMVar_hsa_circ_372212,RMVar_hsa_circ_65107,RMVar_hsa_circ_197348,RMVar_hsa_circ_373409,RMVar_hsa_circ_330358,RMVar_hsa_circ_197347 31585 RMVar_ID_31585 Human_SNP_ID_62985368 A-to-I Human chr2 - 20271996 20271996 20271996 TGCCAGCACGCCCAGCTAATTTCTGTATTTTTAGTAGAGACGGGTTTTCACCATGTTGGTCAGGC TGCCAGCACGCCCAGCTAATTTCTGTATTTTTGGTAGAGACGGGTTTTCACCATGTTGGTCAGGC T C PUM2 Ensembl:ENSG00000055917 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1244708834 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29978,RMVar_hsa_circ_126586,RMVar_hsa_circ_78595,RMVar_hsa_circ_334160,RMVar_hsa_circ_45098,RMVar_hsa_circ_197337,RMVar_hsa_circ_375893,RMVar_hsa_circ_197339,RMVar_hsa_circ_110711,RMVar_hsa_circ_197340,RMVar_hsa_circ_197338,RMVar_hsa_circ_40888,RMVar_hsa_circ_48130,RMVar_hsa_circ_39090,RMVar_hsa_circ_50340,RMVar_hsa_circ_87928,RMVar_hsa_circ_197346,RMVar_hsa_circ_197345,RMVar_hsa_circ_372212,RMVar_hsa_circ_65107,RMVar_hsa_circ_197348,RMVar_hsa_circ_373409,RMVar_hsa_circ_330358,RMVar_hsa_circ_197347 31586 RMVar_ID_31586 Human_SNP_ID_62985382 A-to-I Human chr2 - 20272047 20272047 20272047 TCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGTGGGGATTACAGGCGCCTGCCAGCACGCCCA TCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTGGTGGGGATTACAGGCGCCTGCCAGCACGCCCA T C PUM2 Ensembl:ENSG00000055917 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1329539005 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25503088 RMVar_hsa_circ_29978,RMVar_hsa_circ_126586,RMVar_hsa_circ_78595,RMVar_hsa_circ_334160,RMVar_hsa_circ_45098,RMVar_hsa_circ_197337,RMVar_hsa_circ_375893,RMVar_hsa_circ_197339,RMVar_hsa_circ_110711,RMVar_hsa_circ_197340,RMVar_hsa_circ_197338,RMVar_hsa_circ_40888,RMVar_hsa_circ_48130,RMVar_hsa_circ_39090,RMVar_hsa_circ_50340,RMVar_hsa_circ_87928,RMVar_hsa_circ_197346,RMVar_hsa_circ_197345,RMVar_hsa_circ_372212,RMVar_hsa_circ_65107,RMVar_hsa_circ_197348,RMVar_hsa_circ_373409,RMVar_hsa_circ_330358,RMVar_hsa_circ_197347 31587 RMVar_ID_31587 Human_SNP_ID_62985391 A-to-I Human chr2 - 20272076 20272076 20272076 TTCAGCTCACTGCAGCCTGTCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGTG TTCAGCTCACTGCAGCCTGTCTCCCAGGTTCAGGCGATTCTCCTGCCTCAGCCTCCTGAGTAGTG T C PUM2 Ensembl:ENSG00000055917 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1206350044 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29978,RMVar_hsa_circ_126586,RMVar_hsa_circ_78595,RMVar_hsa_circ_334160,RMVar_hsa_circ_45098,RMVar_hsa_circ_197337,RMVar_hsa_circ_375893,RMVar_hsa_circ_197339,RMVar_hsa_circ_110711,RMVar_hsa_circ_197340,RMVar_hsa_circ_197338,RMVar_hsa_circ_40888,RMVar_hsa_circ_48130,RMVar_hsa_circ_39090,RMVar_hsa_circ_50340,RMVar_hsa_circ_87928,RMVar_hsa_circ_197346,RMVar_hsa_circ_197345,RMVar_hsa_circ_372212,RMVar_hsa_circ_65107,RMVar_hsa_circ_197348,RMVar_hsa_circ_373409,RMVar_hsa_circ_330358,RMVar_hsa_circ_197347 31588 RMVar_ID_31588 Human_SNP_ID_62990545 A-to-I Human chr2 - 20292439 20292439 20292439 AGAAGCACTTGAATCCAGGAGGTAGAGGTTGCAGTGAGCTGAGATCATGCCATTGCACTCCAGCC AGAAGCACTTGAATCCAGGAGGTAGAGGTTGCCGTGAGCTGAGATCATGCCATTGCACTCCAGCC T G PUM2 Ensembl:ENSG00000055917 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs986672049 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78595,RMVar_hsa_circ_45098,RMVar_hsa_circ_197337,RMVar_hsa_circ_40888,RMVar_hsa_circ_48130,RMVar_hsa_circ_197348,RMVar_hsa_circ_373409,RMVar_hsa_circ_197357,RMVar_hsa_circ_103965,RMVar_hsa_circ_197351,RMVar_hsa_circ_283399,RMVar_hsa_circ_303062,RMVar_hsa_circ_339521,RMVar_hsa_circ_296215,RMVar_hsa_circ_266528,RMVar_hsa_circ_197359,RMVar_hsa_circ_197361,RMVar_hsa_circ_102764,RMVar_hsa_circ_197362,RMVar_hsa_circ_197360,RMVar_hsa_circ_197358,RMVar_hsa_circ_365670,RMVar_hsa_circ_270640,RMVar_hsa_circ_321864,RMVar_hsa_circ_266627,RMVar_hsa_circ_88779,RMVar_hsa_circ_197367,RMVar_hsa_circ_197364,RMVar_hsa_circ_197365,RMVar_hsa_circ_197363,RMVar_hsa_circ_84427,RMVar_hsa_circ_335442,RMVar_hsa_circ_375966,RMVar_hsa_circ_294573,RMVar_hsa_circ_197370,RMVar_hsa_circ_39167,RMVar_hsa_circ_54182,RMVar_hsa_circ_197372,RMVar_hsa_circ_25949,RMVar_hsa_circ_197371,RMVar_hsa_circ_197368,RMVar_hsa_circ_197369 31589 RMVar_ID_31589 Human_SNP_ID_62990667 A-to-I Human chr2 - 20292875 20292875 20292875 TTGCCCAGACTGGAGTGCAATGGAGTGATCTCAGCTCACCACAACCTCTGCCTCCCGGCAGCAAT TTGCCCAGACTGGAGTGCAATGGAGTGATCTCTGCTCACCACAACCTCTGCCTCCCGGCAGCAAT T A PUM2 Ensembl:ENSG00000055917 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs991159250 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25503433 RMVar_hsa_circ_78595,RMVar_hsa_circ_45098,RMVar_hsa_circ_197337,RMVar_hsa_circ_40888,RMVar_hsa_circ_48130,RMVar_hsa_circ_197348,RMVar_hsa_circ_373409,RMVar_hsa_circ_197357,RMVar_hsa_circ_103965,RMVar_hsa_circ_197351,RMVar_hsa_circ_283399,RMVar_hsa_circ_303062,RMVar_hsa_circ_339521,RMVar_hsa_circ_296215,RMVar_hsa_circ_266528,RMVar_hsa_circ_197359,RMVar_hsa_circ_197361,RMVar_hsa_circ_102764,RMVar_hsa_circ_197362,RMVar_hsa_circ_197360,RMVar_hsa_circ_197358,RMVar_hsa_circ_365670,RMVar_hsa_circ_270640,RMVar_hsa_circ_321864,RMVar_hsa_circ_266627,RMVar_hsa_circ_88779,RMVar_hsa_circ_197367,RMVar_hsa_circ_197364,RMVar_hsa_circ_197365,RMVar_hsa_circ_197363,RMVar_hsa_circ_84427,RMVar_hsa_circ_335442,RMVar_hsa_circ_375966,RMVar_hsa_circ_294573,RMVar_hsa_circ_197370,RMVar_hsa_circ_39167,RMVar_hsa_circ_54182,RMVar_hsa_circ_197372,RMVar_hsa_circ_25949,RMVar_hsa_circ_197371,RMVar_hsa_circ_197368,RMVar_hsa_circ_197369 31590 RMVar_ID_31590 Human_SNP_ID_62990668 A-to-I Human chr2 - 20292875 20292875 20292875 TTGCCCAGACTGGAGTGCAATGGAGTGATCTCAGCTCACCACAACCTCTGCCTCCCGGCAGCAAT TTGCCCAGACTGGAGTGCAATGGAGTGATCTCGGCTCACCACAACCTCTGCCTCCCGGCAGCAAT T C PUM2 Ensembl:ENSG00000055917 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs991159250 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25503433 RMVar_hsa_circ_78595,RMVar_hsa_circ_45098,RMVar_hsa_circ_197337,RMVar_hsa_circ_40888,RMVar_hsa_circ_48130,RMVar_hsa_circ_197348,RMVar_hsa_circ_373409,RMVar_hsa_circ_197357,RMVar_hsa_circ_103965,RMVar_hsa_circ_197351,RMVar_hsa_circ_283399,RMVar_hsa_circ_303062,RMVar_hsa_circ_339521,RMVar_hsa_circ_296215,RMVar_hsa_circ_266528,RMVar_hsa_circ_197359,RMVar_hsa_circ_197361,RMVar_hsa_circ_102764,RMVar_hsa_circ_197362,RMVar_hsa_circ_197360,RMVar_hsa_circ_197358,RMVar_hsa_circ_365670,RMVar_hsa_circ_270640,RMVar_hsa_circ_321864,RMVar_hsa_circ_266627,RMVar_hsa_circ_88779,RMVar_hsa_circ_197367,RMVar_hsa_circ_197364,RMVar_hsa_circ_197365,RMVar_hsa_circ_197363,RMVar_hsa_circ_84427,RMVar_hsa_circ_335442,RMVar_hsa_circ_375966,RMVar_hsa_circ_294573,RMVar_hsa_circ_197370,RMVar_hsa_circ_39167,RMVar_hsa_circ_54182,RMVar_hsa_circ_197372,RMVar_hsa_circ_25949,RMVar_hsa_circ_197371,RMVar_hsa_circ_197368,RMVar_hsa_circ_197369 31591 RMVar_ID_31591 Human_SNP_ID_62992374 A-to-I Human chr2 - 20299505 20299505 20299505 TGCTACCACACCCAGCTAATTTTTATATTTTTAGCAGAGACGGGGTTTCACTGTGTTCAAGACCA TGCTACCACACCCAGCTAATTTTTATATTTTTGGCAGAGACGGGGTTTCACTGTGTTCAAGACCA T C PUM2 Ensembl:ENSG00000055917 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1447710847 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14014004 RMVar_hsa_circ_1472,RMVar_hsa_circ_45098,RMVar_hsa_circ_40888,RMVar_hsa_circ_48130,RMVar_hsa_circ_197348,RMVar_hsa_circ_373409,RMVar_hsa_circ_103965,RMVar_hsa_circ_197351,RMVar_hsa_circ_339521,RMVar_hsa_circ_296215,RMVar_hsa_circ_266528,RMVar_hsa_circ_197359,RMVar_hsa_circ_197361,RMVar_hsa_circ_102764,RMVar_hsa_circ_197362,RMVar_hsa_circ_197360,RMVar_hsa_circ_197358,RMVar_hsa_circ_365670,RMVar_hsa_circ_270640,RMVar_hsa_circ_266627,RMVar_hsa_circ_88779,RMVar_hsa_circ_197367,RMVar_hsa_circ_197364,RMVar_hsa_circ_197363,RMVar_hsa_circ_84427,RMVar_hsa_circ_294573,RMVar_hsa_circ_197370,RMVar_hsa_circ_39167,RMVar_hsa_circ_54182,RMVar_hsa_circ_197372,RMVar_hsa_circ_25949,RMVar_hsa_circ_197371,RMVar_hsa_circ_276126,RMVar_hsa_circ_91078,RMVar_hsa_circ_34098,RMVar_hsa_circ_197373,RMVar_hsa_circ_197374,RMVar_hsa_circ_277085,RMVar_hsa_circ_345271,RMVar_hsa_circ_108156,RMVar_hsa_circ_197378,RMVar_hsa_circ_197379,RMVar_hsa_circ_197377 31592 RMVar_ID_31592 Human_SNP_ID_62994359 A-to-I Human chr2 - 20307134 20307134 20307134 TCGGCTCACTTCAGCCTCCGCCTTCTGGGTTCAAGAGATTCTCCTGCCTCAGCCTTCTGAGTAGC TCGGCTCACTTCAGCCTCCGCCTTCTGGGTTCTAGAGATTCTCCTGCCTCAGCCTTCTGAGTAGC T A PUM2 Ensembl:ENSG00000055917 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1030534958 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1472,RMVar_hsa_circ_45098,RMVar_hsa_circ_40888,RMVar_hsa_circ_48130,RMVar_hsa_circ_197348,RMVar_hsa_circ_373409,RMVar_hsa_circ_103965,RMVar_hsa_circ_197351,RMVar_hsa_circ_339521,RMVar_hsa_circ_296215,RMVar_hsa_circ_266528,RMVar_hsa_circ_197359,RMVar_hsa_circ_197361,RMVar_hsa_circ_102764,RMVar_hsa_circ_197362,RMVar_hsa_circ_197360,RMVar_hsa_circ_197358,RMVar_hsa_circ_365670,RMVar_hsa_circ_270640,RMVar_hsa_circ_266627,RMVar_hsa_circ_88779,RMVar_hsa_circ_197367,RMVar_hsa_circ_197364,RMVar_hsa_circ_197363,RMVar_hsa_circ_84427,RMVar_hsa_circ_294573,RMVar_hsa_circ_197370,RMVar_hsa_circ_39167,RMVar_hsa_circ_54182,RMVar_hsa_circ_197372,RMVar_hsa_circ_25949,RMVar_hsa_circ_197371,RMVar_hsa_circ_276126,RMVar_hsa_circ_91078,RMVar_hsa_circ_34098,RMVar_hsa_circ_197373,RMVar_hsa_circ_197374,RMVar_hsa_circ_277085,RMVar_hsa_circ_345271,RMVar_hsa_circ_108156,RMVar_hsa_circ_197378,RMVar_hsa_circ_197379,RMVar_hsa_circ_197377 31593 RMVar_ID_31593 Human_SNP_ID_63001589 A-to-I Human chr2 - 20334262 20334262 20334262 GTCACCCAATCTGGAGTGCAGTGGAGCGGACCATGGCTCACTGCAGTCTTGACCTCCCAGACTCA GTCACCCAATCTGGAGTGCAGTGGAGCGGACCGTGGCTCACTGCAGTCTTGACCTCCCAGACTCA T C PUM2 Ensembl:ENSG00000055917 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs774579247 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13749851,Human_RBP_ID_25503783 31594 RMVar_ID_31594 Human_SNP_ID_63001803 A-to-I Human chr2 - 20335056 20335056 20335056 TGCTGGGGGTGGTGGCATGCACCTTTAGTCCCAGATACTCCCGGAGACTGAGGTGAGAGGATGCA TGCTGGGGGTGGTGGCATGCACCTTTAGTCCCTGATACTCCCGGAGACTGAGGTGAGAGGATGCA T A PUM2 Ensembl:ENSG00000055917 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs984752448 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18753205,Human_RBP_ID_25503789 31595 RMVar_ID_31595 Human_SNP_ID_63002144 A-to-I Human chr2 - 20336254 20336254 20336254 TAGCCCAGGAGGTCAAGGCTGTAGTGAGCCATAATCAATGCCACTGCACTCCATCCTGGGCAATA TAGCCCAGGAGGTCAAGGCTGTAGTGAGCCATGATCAATGCCACTGCACTCCATCCTGGGCAATA T C PUM2 Ensembl:ENSG00000055917 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559954533 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13749930 31596 RMVar_ID_31596 Human_SNP_ID_63002163 A-to-I Human chr2 - 20336323 20336323 20336323 AAAATTAGTTGGGCATAGTGGTATGCATTTGTAGTCCCAGCTCCTTAGGATACTGAGTAGATGGA AAAATTAGTTGGGCATAGTGGTATGCATTTGTTGTCCCAGCTCCTTAGGATACTGAGTAGATGGA T A PUM2 Ensembl:ENSG00000055917 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1222971536 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2616518,Human_RBP_ID_13749930 31597 RMVar_ID_31597 Human_SNP_ID_63003150 A-to-I Human chr2 - 20339700 20339700 20339700 AAGTTTTATATTTTTAGTAGAGACAGGGTTTCACCATGTCTGCTAGGCTGGTCTTGAACTCCTGA AAGTTTTATATTTTTAGTAGAGACAGGGTTTCGCCATGTCTGCTAGGCTGGTCTTGAACTCCTGA T C PUM2 Ensembl:ENSG00000055917 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs932544611 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13750067 31598 RMVar_ID_31598 Human_SNP_ID_63004206 A-to-I Human chr2 - 20343846 20343846 20343846 CTGCTCACTGCAGCCTCAACTGCCCAGTCTCAAGCAGTTCTCTGACTTCAGCCTCCTGAGGAGCT CTGCTCACTGCAGCCTCAACTGCCCAGTCTCAGGCAGTTCTCTGACTTCAGCCTCCTGAGGAGCT T C PUM2 Ensembl:ENSG00000055917 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1470495718 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13750284 31599 RMVar_ID_31599 Human_SNP_ID_63004209 A-to-I Human chr2 - 20343853 20343853 20343853 GCAGTCACTGCTCACTGCAGCCTCAACTGCCCAGTCTCAAGCAGTTCTCTGACTTCAGCCTCCTG GCAGTCACTGCTCACTGCAGCCTCAACTGCCCGGTCTCAAGCAGTTCTCTGACTTCAGCCTCCTG T C PUM2 Ensembl:ENSG00000055917 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1034681063 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13750285 31600 RMVar_ID_31600 Human_SNP_ID_63004676 A-to-I Human chr2 - 20345192 20345192 20345192 GTGGGAATGAGGTGGGAAGGTCACTTGAATCCAGGAGACTGAGGCTGCAGTGAGTTGTGATCGTG GTGGGAATGAGGTGGGAAGGTCACTTGAATCCGGGAGACTGAGGCTGCAGTGAGTTGTGATCGTG T C PUM2 Ensembl:ENSG00000055917 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,cerebellum - 29129909,30559470 RNA-Seq:(High) rs1043245839 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5194778,Human_RBP_ID_6877517,Human_RBP_ID_13750355,Human_RBP_ID_17569445 31601 RMVar_ID_31601 Human_SNP_ID_63004691 A-to-I Human chr2 - 20345249 20345249 20345249 AAAATTAGTCTGGCATGGTGGCACGCACTTACAGTCCAAGCTATTTGGGAGGCTGAGGTGGGAAT AAAATTAGTCTGGCATGGTGGCACGCACTTACCGTCCAAGCTATTTGGGAGGCTGAGGTGGGAAT T G PUM2 Ensembl:ENSG00000055917 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444979580 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13750372,Human_RBP_ID_25503915 31602 RMVar_ID_31602 Human_SNP_ID_63038506 A-to-I Human chr2 - 20478188 20478188 20478188 AGCTGTAGCAGGAAAAGAAGTAACAGTCACTCATTTTGGCCAAGAGGGGGTGTTTGGTATTTCGC AGCTGTAGCAGGAAAAGAAGTAACAGTCACTCGTTTTGGCCAAGAGGGGGTGTTTGGTATTTCGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs577865973 Functional Loss SNV dbSNP153 33..33 33 - - - 31603 RMVar_ID_31603 Human_SNP_ID_63053825 A-to-I Human chr2 + 20533617 20533617 20533617 TTTAGTAGAGACTGGGTTTCACCGTGTTGCCCAAGCTGTTCGCGAATTCCTGAACTCAGGCAGTC TTTAGTAGAGACTGGGTTTCACCGTGTTGCCCGAGCTGTTCGCGAATTCCTGAACTCAGGCAGTC A G lnc-GDF7-4,NONHSAG027165.2 RNACentral:URS00008BAAE5,RNACentral:URS00009BEBEF lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1262540591 Functional Loss SNV dbSNP153 33..33 33 - - - 31604 RMVar_ID_31604 Human_SNP_ID_63843501 A-to-I Human chr2 + 23678408 23678405 23678409 AGCTATGGCCTCAAGAAGCTTTGCTCACTTTCACTCACTCTCCGGGGACCCCTGGCACCACTATC AGCTATGGCCTCAAGAAGCTTTGCTCACTT____TCACTCTCCGGGGACCCCTGGCACCACTATC TTCAC T KLHL29 Ensembl:ENSG00000119771 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1476695709 Functional Loss DEL dbSNP153 31..34 33 - - - RMVar_hsa_circ_33854 31605 RMVar_ID_31605 Human_SNP_ID_63843748 A-to-I Human chr2 + 23679459 23679459 23679459 TGGAGAGTGAGTGAAAGTGAGCAAAGCTTCTTAAGGCCGTGACTCACATTTTCACAGGGTCACTT TGGAGAGTGAGTGAAAGTGAGCAAAGCTTCTTGAGGCCGTGACTCACATTTTCACAGGGTCACTT A G KLHL29 Ensembl:ENSG00000119771 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs957223298 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33854 31606 RMVar_ID_31606 Human_SNP_ID_63868311 A-to-I Human chr2 - 23779316 23779316 23779316 AAAAAATTAGCGAGGCGTGGTGGTGGGCGCCTATAGTCACAGCTACTCAGGAGGCTGAGGCAGGG AAAAAATTAGCGAGGCGTGGTGGTGGGCGCCTGTAGTCACAGCTACTCAGGAGGCTGAGGCAGGG T C ATAD2B Ensembl:ENSG00000119778 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251944272 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 31607 RMVar_ID_31607 Human_SNP_ID_63887326 A-to-I Human chr2 - 23858682 23858682 23858682 GCCCAAGAGTTTGAGACCATCCCGGGCAACATAGTGAGAACTCATCTCTCCAAATACTTAAAAAT GCCCAAGAGTTTGAGACCATCCCGGGCAACATGGTGAGAACTCATCTCTCCAAATACTTAAAAAT T C ATAD2B Ensembl:ENSG00000119778 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1240103757 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_98821,RMVar_hsa_circ_197480,RMVar_hsa_circ_21159,RMVar_hsa_circ_124269,RMVar_hsa_circ_295520,RMVar_hsa_circ_317866,RMVar_hsa_circ_74695,RMVar_hsa_circ_120187,RMVar_hsa_circ_47341,RMVar_hsa_circ_197491,RMVar_hsa_circ_197489,RMVar_hsa_circ_197490,RMVar_hsa_circ_33627,RMVar_hsa_circ_74689,RMVar_hsa_circ_350049,RMVar_hsa_circ_44510,RMVar_hsa_circ_30814,RMVar_hsa_circ_86482,RMVar_hsa_circ_340699,RMVar_hsa_circ_88894,RMVar_hsa_circ_75431,RMVar_hsa_circ_79389,RMVar_hsa_circ_197513,RMVar_hsa_circ_197515,RMVar_hsa_circ_197516,RMVar_hsa_circ_197514,RMVar_hsa_circ_197519,RMVar_hsa_circ_273072,RMVar_hsa_circ_305502,RMVar_hsa_circ_340077,RMVar_hsa_circ_378242,RMVar_hsa_circ_370511,RMVar_hsa_circ_309152,RMVar_hsa_circ_286104,RMVar_hsa_circ_302561,RMVar_hsa_circ_281740,RMVar_hsa_circ_63047,RMVar_hsa_circ_197521,RMVar_hsa_circ_197522,RMVar_hsa_circ_197520,RMVar_hsa_circ_197518 31608 RMVar_ID_31608 Human_SNP_ID_63892131 A-to-I Human chr2 - 23877646 23877646 23877646 GCTGGTCTTGAACTCCTGACCTCTCGTGATCCACCCGCCTTAGCCTCCCAAAGTGCTGGGATTAC GCTGGTCTTGAACTCCTGACCTCTCGTGATCCCCCCGCCTTAGCCTCCCAAAGTGCTGGGATTAC T G ATAD2B Ensembl:ENSG00000119778 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs939671195 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13817736 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_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_197531 31609 RMVar_ID_31609 Human_SNP_ID_63893330 A-to-I Human chr2 - 23881870 23881870 23881870 GAAAATACAAAATTAGCCAAGCATGGTGATACATGCTTGTAGTCCCAGCTACTCAGGAGGCTGAG GAAAATACAAAATTAGCCAAGCATGGTGATACGTGCTTGTAGTCCCAGCTACTCAGGAGGCTGAG T C ATAD2B Ensembl:ENSG00000119778 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs912992943 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_197489,RMVar_hsa_circ_197490,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_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_197532,RMVar_hsa_circ_272148,RMVar_hsa_circ_280436,RMVar_hsa_circ_197527,RMVar_hsa_circ_278436,RMVar_hsa_circ_197533,RMVar_hsa_circ_197537,RMVar_hsa_circ_319069,RMVar_hsa_circ_197531,RMVar_hsa_circ_303639,RMVar_hsa_circ_283325,RMVar_hsa_circ_197536 31610 RMVar_ID_31610 Human_SNP_ID_63895992 A-to-I Human chr2 - 23891653 23891653 23891653 GAAACCCTGTCTACACTAAAAATACAAAAATTAGCCAGGTGTGGTGGTGCACGCCTGTACTGCTT GAAACCCTGTCTACACTAAAAATACAAAAATTGGCCAGGTGTGGTGGTGCACGCCTGTACTGCTT T C ATAD2B Ensembl:ENSG00000119778 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1338819297 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_330779,RMVar_hsa_circ_316297,RMVar_hsa_circ_295520,RMVar_hsa_circ_281740,RMVar_hsa_circ_13830,RMVar_hsa_circ_197518,RMVar_hsa_circ_346006,RMVar_hsa_circ_278436,RMVar_hsa_circ_197533,RMVar_hsa_circ_197537,RMVar_hsa_circ_303639,RMVar_hsa_circ_289417,RMVar_hsa_circ_197539,RMVar_hsa_circ_357642,RMVar_hsa_circ_300488 31611 RMVar_ID_31611 Human_SNP_ID_63895993 A-to-I Human chr2 - 23891656 23891655 23891656 AGTGAAACCCTGTCTACACTAAAAATACAAAAATTAGCCAGGTGTGGTGGTGCACGCCTGTACTG AGTGAAACCCTGTCTACACTAAAAATACAAAA_TTAGCCAGGTGTGGTGGTGCACGCCTGTACTG AT A ATAD2B Ensembl:ENSG00000119778 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1310623731 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_330779,RMVar_hsa_circ_316297,RMVar_hsa_circ_295520,RMVar_hsa_circ_281740,RMVar_hsa_circ_13830,RMVar_hsa_circ_197518,RMVar_hsa_circ_346006,RMVar_hsa_circ_278436,RMVar_hsa_circ_197533,RMVar_hsa_circ_197537,RMVar_hsa_circ_303639,RMVar_hsa_circ_289417,RMVar_hsa_circ_197539,RMVar_hsa_circ_357642,RMVar_hsa_circ_300488 31612 RMVar_ID_31612 Human_SNP_ID_63896558 A-to-I Human chr2 - 23893808 23893808 23893808 TACTAAAAAATTAGCTTCAGGCACATGCTTGTAGTCCGATCTACTCGAAAGGCTAAGGCTGGAGG TACTAAAAAATTAGCTTCAGGCACATGCTTGTGGTCCGATCTACTCGAAAGGCTAAGGCTGGAGG T C ATAD2B Ensembl:ENSG00000119778 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1177486906 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_330779,RMVar_hsa_circ_316297,RMVar_hsa_circ_295520,RMVar_hsa_circ_281740,RMVar_hsa_circ_13830,RMVar_hsa_circ_197518,RMVar_hsa_circ_346006,RMVar_hsa_circ_278436,RMVar_hsa_circ_197533,RMVar_hsa_circ_197537,RMVar_hsa_circ_303639,RMVar_hsa_circ_289417,RMVar_hsa_circ_197539,RMVar_hsa_circ_357642,RMVar_hsa_circ_300488 31613 RMVar_ID_31613 Human_SNP_ID_63899568 A-to-I Human chr2 - 23906265 23906265 23906265 GCCACCTCGGCTCACTGCAGCCTCCGCCTTCCAGGTTCAAGTGATTCTCCTGTCTCAGTCTCCTG GCCACCTCGGCTCACTGCAGCCTCCGCCTTCCTGGTTCAAGTGATTCTCCTGTCTCAGTCTCCTG T A ATAD2B Ensembl:ENSG00000119778 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1287461705 Functional Loss SNV dbSNP153 33..33 33 - - - 31614 RMVar_ID_31614 Human_SNP_ID_63909703 A-to-I Human chr2 + 23943215 23943215 23943215 CAGACCTTCTGATCTGCCCACTTCAGCCTCCCAAAGTGCTGGAATTACAGGCGTGAGCCACCGTG CAGACCTTCTGATCTGCCCACTTCAGCCTCCCGAAGTGCTGGAATTACAGGCGTGAGCCACCGTG A G UBXN2A Ensembl:ENSG00000173960 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005499501 Functional Loss SNV dbSNP153 33..33 33 - - - 31615 RMVar_ID_31615 Human_SNP_ID_63911354 A-to-I Human chr2 + 23949832 23949832 23949832 AGGAGGCGGAGGTTGCAGTAAGCTGAGACCTCACCACTGCACTCTAGCCTGGGCAACAGAGCAAG AGGAGGCGGAGGTTGCAGTAAGCTGAGACCTCCCCACTGCACTCTAGCCTGGGCAACAGAGCAAG A C UBXN2A Ensembl:ENSG00000173960 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs970569274 Functional Loss SNV dbSNP153 33..33 33 - - - 31616 RMVar_ID_31616 Human_SNP_ID_63920417 A-to-I Human chr2 + 23984981 23984981 23984981 CAGAGTGCAGTGGCACAGTCATAGCTCACTGCAGTCTTGAAGTCCTGGATTCAAGCAATCCTCCC CAGAGTGCAGTGGCACAGTCATAGCTCACTGCGGTCTTGAAGTCCTGGATTCAAGCAATCCTCCC A G UBXN2A Ensembl:ENSG00000173960 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs896310840 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_197541,RMVar_hsa_circ_197549 31617 RMVar_ID_31617 Human_SNP_ID_63920422 A-to-I Human chr2 + 23985001 23985001 23985001 ATAGCTCACTGCAGTCTTGAAGTCCTGGATTCAAGCAATCCTCCCACCTCAGCCTCCTGAGTTGT ATAGCTCACTGCAGTCTTGAAGTCCTGGATTCGAGCAATCCTCCCACCTCAGCCTCCTGAGTTGT A G UBXN2A Ensembl:ENSG00000173960 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1013337563 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_197541,RMVar_hsa_circ_197549 31618 RMVar_ID_31618 Human_SNP_ID_63921487 A-to-I Human chr2 + 23989365 23989365 23989365 TCACTCTGTCTCCCAGGTTGGAGTGTAGTGGTATAATTACAGATCACTGCAGCCTCCACCTCCCC TCACTCTGTCTCCCAGGTTGGAGTGTAGTGGTGTAATTACAGATCACTGCAGCCTCCACCTCCCC A G UBXN2A Ensembl:ENSG00000173960 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1265402738 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_197541,RMVar_hsa_circ_197549 31619 RMVar_ID_31619 Human_SNP_ID_63923104 A-to-I Human chr2 + 23996269 23996269 23996269 TTTATATTTTTAGTAGAAACAGTGTTCACCATATTGGCCAGGCTGGTCTTGAACTCCTGAACTCA TTTATATTTTTAGTAGAAACAGTGTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGAACTCA A G UBXN2A Ensembl:ENSG00000173960 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1415269125 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13821299 RMVar_hsa_circ_197541,RMVar_hsa_circ_197549 31620 RMVar_ID_31620 Human_SNP_ID_63924026 A-to-I Human chr2 + 24000272 24000272 24000272 TGAGTTTTTAAATAGCTAATACGACCGGGTACAGTGGTTCATGCCTGTAATCCCAGAACTTCGGG TGAGTTTTTAAATAGCTAATACGACCGGGTACGGTGGTTCATGCCTGTAATCCCAGAACTTCGGG A G UBXN2A Ensembl:ENSG00000173960 Protein coding exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1302089080 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_547039 31621 RMVar_ID_31621 Human_SNP_ID_63924063 A-to-I Human chr2 + 24000386 24000386 24000386 AAACATGGTGAAACCCCATCTCTAGTAAAAATACAAAAATTAGCTGGGCGTGGCGGTGCGCAACT AAACATGGTGAAACCCCATCTCTAGTAAAAATGCAAAAATTAGCTGGGCGTGGCGGTGCGCAACT A G UBXN2A Ensembl:ENSG00000173960 Protein coding exon GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1170640356 Functional Loss SNV dbSNP153 33..33 33 - - - 31622 RMVar_ID_31622 Human_SNP_ID_63924077 A-to-I Human chr2 + 24000421 24000421 24000421 AAAATTAGCTGGGCGTGGCGGTGCGCAACTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTAGCTGGGCGTGGCGGTGCGCAACTGTGGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA A G UBXN2A Ensembl:ENSG00000173960 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1407473519 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_276252,Human_miRNA_ID_1803010 31623 RMVar_ID_31623 Human_SNP_ID_63924078 A-to-I Human chr2 + 24000431 24000431 24000431 GGGCGTGGCGGTGCGCAACTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCTCTTGAA GGGCGTGGCGGTGCGCAACTGTAGTCCCAGCTGCTCGGGAGGCTGAGGCAGGAGAATCTCTTGAA A G UBXN2A Ensembl:ENSG00000173960 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334092888 Functional Loss SNV dbSNP153 33..33 33 - - - 31624 RMVar_ID_31624 Human_SNP_ID_63924084 A-to-I Human chr2 + 24000448 24000448 24000448 ACTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCTCTTGAACCTGGCAAGTGTAGGTT ACTGTAGTCCCAGCTACTCGGGAGGCTGAGGCGGGAGAATCTCTTGAACCTGGCAAGTGTAGGTT A G UBXN2A Ensembl:ENSG00000173960 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1185494817 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13822157 31625 RMVar_ID_31625 Human_SNP_ID_63924112 A-to-I Human chr2 + 24000592 24000592 24000592 TAAAATAAATATAAATAATTGTGGCCGGGTGCAATGGCTCATGCCTGTAATCCCAGCACTTTGGG TAAAATAAATATAAATAATTGTGGCCGGGTGCGATGGCTCATGCCTGTAATCCCAGCACTTTGGG A G UBXN2A Ensembl:ENSG00000173960 Protein coding exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1204175372 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17953822 Human_miRNA_ID_685518,Human_miRNA_ID_888064,Human_miRNA_ID_1064705,Human_miRNA_ID_1076020 31626 RMVar_ID_31626 Human_SNP_ID_63924234 A-to-I Human chr2 + 24001120 24001120 24001120 TTCAAGAGATTCTCCTGCTCAGCCTCCCAAGTAGCTGGGATTACAGGCATGCGCCACCATGCTTG TTCAAGAGATTCTCCTGCTCAGCCTCCCAAGTTGCTGGGATTACAGGCATGCGCCACCATGCTTG A T UBXN2A Ensembl:ENSG00000173960 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs941173461 Functional Loss SNV dbSNP153 33..33 33 - - - 31627 RMVar_ID_31627 Human_SNP_ID_63924242 A-to-I Human chr2 + 24001170 24001170 24001170 GCGCCACCATGCTTGGCTAATTTTGCATTTTTAGTAGACACGGGATTTCACCATGTTGGTCAGGC GCGCCACCATGCTTGGCTAATTTTGCATTTTTGGTAGACACGGGATTTCACCATGTTGGTCAGGC A G UBXN2A Ensembl:ENSG00000173960 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs933693166 Functional Loss SNV dbSNP153 33..33 33 - - - 31628 RMVar_ID_31628 Human_SNP_ID_63924243 A-to-I Human chr2 + 24001170 24001170 24001170 GCGCCACCATGCTTGGCTAATTTTGCATTTTTAGTAGACACGGGATTTCACCATGTTGGTCAGGC GCGCCACCATGCTTGGCTAATTTTGCATTTTTTGTAGACACGGGATTTCACCATGTTGGTCAGGC A T UBXN2A Ensembl:ENSG00000173960 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs933693166 Functional Loss SNV dbSNP153 33..33 33 - - - 31629 RMVar_ID_31629 Human_SNP_ID_63924378 A-to-I Human chr2 + 24001774 24001774 24001774 AAGGTCAAGTGATTGAGACCATCCTGTCCAACATGGTGAATCCCCGTCTCTACTAAAAATACAAA AAGGTCAAGTGATTGAGACCATCCTGTCCAACGTGGTGAATCCCCGTCTCTACTAAAAATACAAA A G UBXN2A Ensembl:ENSG00000173960 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs868232638 Functional Loss SNV dbSNP153 33..33 33 - - - 31630 RMVar_ID_31630 Human_SNP_ID_63924397 A-to-I Human chr2 + 24001840 24001840 24001840 AAAATTAGCTGGGTGTGGTGGCATGCGCCTGTAGTCCCAGCTACGTGGGAGGCTGAGGGAGGAGA AAAATTAGCTGGGTGTGGTGGCATGCGCCTGTGGTCCCAGCTACGTGGGAGGCTGAGGGAGGAGA A G UBXN2A Ensembl:ENSG00000173960 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1451296464 Functional Loss SNV dbSNP153 33..33 33 - - - 31631 RMVar_ID_31631 Human_SNP_ID_63924422 A-to-I Human chr2 + 24001906 24001906 24001906 TGGCTTGAACCCGGGAGGTGGAGGTTTCAGTGAGCCGAGATTGCGCCCCTGCACTCCAGCCTGGT TGGCTTGAACCCGGGAGGTGGAGGTTTCAGTGGGCCGAGATTGCGCCCCTGCACTCCAGCCTGGT A G UBXN2A Ensembl:ENSG00000173960 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1366053509 Functional Loss SNV dbSNP153 33..33 33 - - - 31632 RMVar_ID_31632 Human_SNP_ID_63924482 A-to-I Human chr2 + 24002136 24002136 24002136 CTATCTATAAAAATTACAAAAATTAGTGCAGTAGCTCACACCTGTAATCCCAGCACTTTGGGACA CTATCTATAAAAATTACAAAAATTAGTGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGACA A G UBXN2A Ensembl:ENSG00000173960 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1161822571 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13822705 31633 RMVar_ID_31633 Human_SNP_ID_63924483 A-to-I Human chr2 + 24002143 24002143 24002143 TAAAAATTACAAAAATTAGTGCAGTAGCTCACACCTGTAATCCCAGCACTTTGGGACACTAAAGC TAAAAATTACAAAAATTAGTGCAGTAGCTCACGCCTGTAATCCCAGCACTTTGGGACACTAAAGC A G UBXN2A Ensembl:ENSG00000173960 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1473130025 Functional Loss SNV dbSNP153 33..33 33 - - - 31634 RMVar_ID_31634 Human_SNP_ID_63924508 A-to-I Human chr2 + 24002243 24002243 24002243 CCTGGTCAATGTGGTGAAACCATGTCTGTACTAAAAATACAAAAATTAGCCTGGTGTGGTGGCAC CCTGGTCAATGTGGTGAAACCATGTCTGTACTGAAAATACAAAAATTAGCCTGGTGTGGTGGCAC A G UBXN2A Ensembl:ENSG00000173960 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1479121325 Functional Loss SNV dbSNP153 33..33 33 - - - 31635 RMVar_ID_31635 Human_SNP_ID_63924509 A-to-I Human chr2 + 24002243 24002243 24002243 CCTGGTCAATGTGGTGAAACCATGTCTGTACTAAAAATACAAAAATTAGCCTGGTGTGGTGGCAC CCTGGTCAATGTGGTGAAACCATGTCTGTACTTAAAATACAAAAATTAGCCTGGTGTGGTGGCAC A T UBXN2A Ensembl:ENSG00000173960 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1479121325 Functional Loss SNV dbSNP153 33..33 33 - - - 31636 RMVar_ID_31636 Human_SNP_ID_63924510 A-to-I Human chr2 + 24002249 24002249 24002249 CAATGTGGTGAAACCATGTCTGTACTAAAAATACAAAAATTAGCCTGGTGTGGTGGCACATGCCT CAATGTGGTGAAACCATGTCTGTACTAAAAATGCAAAAATTAGCCTGGTGTGGTGGCACATGCCT A G UBXN2A Ensembl:ENSG00000173960 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1193012232 Functional Loss SNV dbSNP153 33..33 33 - - - 31637 RMVar_ID_31637 Human_SNP_ID_63924536 A-to-I Human chr2 + 24002307 24002307 24002307 CATGCCTGTAATCTCAGCTACTAGGGAGGCTGAGGGAGGAGAATTGCTTGAACTCAGGAGGCAGA CATGCCTGTAATCTCAGCTACTAGGGAGGCTGGGGGAGGAGAATTGCTTGAACTCAGGAGGCAGA A G UBXN2A Ensembl:ENSG00000173960 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1173274154 Functional Loss SNV dbSNP153 33..33 33 - - - 31638 RMVar_ID_31638 Human_SNP_ID_63924537 A-to-I Human chr2 + 24002311 24002308 24002311 CCTGTAATCTCAGCTACTAGGGAGGCTGAGGGAGGAGAATTGCTTGAACTCAGGAGGCAGAGGTT CCTGTAATCTCAGCTACTAGGGAGGCTGAG___GGAGAATTGCTTGAACTCAGGAGGCAGAGGTT GGGA G UBXN2A Ensembl:ENSG00000173960 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1395584301 Functional Loss DEL dbSNP153 31..33 33 - - - 31639 RMVar_ID_31639 Human_SNP_ID_63924567 A-to-I Human chr2 + 24002411 24002411 24002411 TAGGCAACAGAGTAAGACCCTGCCGTAATAATAATAACTTTTTTTTTTTTGAGATAGAGTTTTGC TAGGCAACAGAGTAAGACCCTGCCGTAATAATGATAACTTTTTTTTTTTTGAGATAGAGTTTTGC A G UBXN2A Ensembl:ENSG00000173960 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs146052501 Functional Loss SNV dbSNP153 33..33 33 - - - 31640 RMVar_ID_31640 Human_SNP_ID_63924583 A-to-I Human chr2 + 24002459 24002459 24002459 TTGAGATAGAGTTTTGCTCTTTCCCCCAGACTAGAGTGCAATGGCGCGATCTTGGCTCACTGCAA TTGAGATAGAGTTTTGCTCTTTCCCCCAGACTGGAGTGCAATGGCGCGATCTTGGCTCACTGCAA A G UBXN2A Ensembl:ENSG00000173960 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1308884455 Functional Loss SNV dbSNP153 33..33 33 - - - 31641 RMVar_ID_31641 Human_SNP_ID_63924585 A-to-I Human chr2 + 24002461 24002461 24002461 GAGATAGAGTTTTGCTCTTTCCCCCAGACTAGAGTGCAATGGCGCGATCTTGGCTCACTGCAACT GAGATAGAGTTTTGCTCTTTCCCCCAGACTAGGGTGCAATGGCGCGATCTTGGCTCACTGCAACT A G UBXN2A Ensembl:ENSG00000173960 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1352803883 Functional Loss SNV dbSNP153 33..33 33 - - - 31642 RMVar_ID_31642 Human_SNP_ID_63924615 A-to-I Human chr2 + 24002549 24002549 24002549 CTTCTGCCACAGCCTCCCGAGTAGCTGGGATTATAGGCGCCCACTACCACGCCTGGCTAATTTTT CTTCTGCCACAGCCTCCCGAGTAGCTGGGATTCTAGGCGCCCACTACCACGCCTGGCTAATTTTT A C UBXN2A Ensembl:ENSG00000173960 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1416926365 Functional Loss SNV dbSNP153 33..33 33 - - - 31643 RMVar_ID_31643 Human_SNP_ID_63924626 A-to-I Human chr2 + 24002590 24002590 24002590 CACTACCACGCCTGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCGCCATGTTGGCCTGGC CACTACCACGCCTGGCTAATTTTTGTATTTTTGGTAGAGACGGGGTTTCGCCATGTTGGCCTGGC A G UBXN2A Ensembl:ENSG00000173960 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1315279991 Functional Loss SNV dbSNP153 33..33 33 - - - 31644 RMVar_ID_31644 Human_SNP_ID_63924661 A-to-I Human chr2 + 24002678 24002678 24002678 GTGATCCGCCCGCCTTGGCCTCCCAAAGTGCTAGGATTATAGGCGTGAGCCACTGTGCCCAGCCA GTGATCCGCCCGCCTTGGCCTCCCAAAGTGCTGGGATTATAGGCGTGAGCCACTGTGCCCAGCCA A G UBXN2A Ensembl:ENSG00000173960 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs1169861689 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_162055 31645 RMVar_ID_31645 Human_SNP_ID_63924662 A-to-I Human chr2 + 24002684 24002684 24002684 CGCCCGCCTTGGCCTCCCAAAGTGCTAGGATTATAGGCGTGAGCCACTGTGCCCAGCCAATAATA CGCCCGCCTTGGCCTCCCAAAGTGCTAGGATTGTAGGCGTGAGCCACTGTGCCCAGCCAATAATA A G UBXN2A Ensembl:ENSG00000173960 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1462059687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_162055,Human_miRNA_ID_1081035 31646 RMVar_ID_31646 Human_SNP_ID_63932776 A-to-I Human chr2 - 24034817 24034817 24034817 TAACCCCAGAACTTTGGGAGGCCGAGATGGGTAGATCACTTGAGTCCAGGAGTTCGAGACCAGCC TAACCCCAGAACTTTGGGAGGCCGAGATGGGTGGATCACTTGAGTCCAGGAGTTCGAGACCAGCC T C WDCP Ensembl:ENSG00000163026 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1009775976 Functional Loss SNV dbSNP153 33..33 33 - - - 31647 RMVar_ID_31647 Human_SNP_ID_63949346 A-to-I Human chr2 - 24100944 24100944 24100944 TTCGTCCATGTCCCTGCAAAGGACATGAACTCATCCTTTTTTATGGCTGCATAGTATTCCATGGT TTCGTCCATGTCCCTGCAAAGGACATGAACTCTTCCTTTTTTATGGCTGCATAGTATTCCATGGT T A - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs528675772 Functional Loss SNV dbSNP153 33..33 33 - - - 31648 RMVar_ID_31648 Human_SNP_ID_63954843 A-to-I Human chr2 + 24125260 24125260 24125260 ACAATAATAGCCAGGTGTGGTAGCATACACCTATAGTCCCAGCTGCTTGAGAGGCTGAGGCAGGA ACAATAATAGCCAGGTGTGGTAGCATACACCTGTAGTCCCAGCTGCTTGAGAGGCTGAGGCAGGA A G FAM228B,AC008073.3 Ensembl:ENSG00000219626,Ensembl:ENSG00000276087 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs184785600 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59128,RMVar_hsa_circ_362225,RMVar_hsa_circ_358728 31649 RMVar_ID_31649 Human_SNP_ID_63986799 A-to-I Human chr2 - 24257244 24257244 24257244 TGGATCATGGCTCACTGCAGCCTCGACCACCCAGCCTTAAGCGATCCTCCCACCTCAGCTTCCCG TGGATCATGGCTCACTGCAGCCTCGACCACCCGGCCTTAAGCGATCCTCCCACCTCAGCTTCCCG T C ITSN2 Ensembl:ENSG00000198399 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1396515887 Functional Loss SNV dbSNP153 33..33 33 - - - 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_305992,RMVar_hsa_circ_334896,RMVar_hsa_circ_358229,RMVar_hsa_circ_326918,RMVar_hsa_circ_273486,RMVar_hsa_circ_77518,RMVar_hsa_circ_25670,RMVar_hsa_circ_64044,RMVar_hsa_circ_41869,RMVar_hsa_circ_197580,RMVar_hsa_circ_197582,RMVar_hsa_circ_197583,RMVar_hsa_circ_197584,RMVar_hsa_circ_197581,RMVar_hsa_circ_197579,RMVar_hsa_circ_31690,RMVar_hsa_circ_32920 31650 RMVar_ID_31650 Human_SNP_ID_64005822 A-to-I Human chr2 - 24335985 24335985 24335985 CACCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCTTGAGCCACCATGCCCGGCCAAGGGAA CACCTGCCTCGGCCTCCCAAAGTGCTGGGATTGCAGGCTTGAGCCACCATGCCCGGCCAAGGGAA T C ITSN2 Ensembl:ENSG00000198399 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900172293 Functional Loss SNV dbSNP153 33..33 33 - - - 31651 RMVar_ID_31651 Human_SNP_ID_64006963 A-to-I Human chr2 - 24339911 24339911 24339911 TCACCTCCTGAGTAGCTACTTCCTGAGTAGCTAGAACTACAGGTGTGTGCCACCATGCCCAACTA TCACCTCCTGAGTAGCTACTTCCTGAGTAGCTGGAACTACAGGTGTGTGCCACCATGCCCAACTA T C ITSN2 Ensembl:ENSG00000198399 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs989783433 Functional Loss SNV dbSNP153 33..33 33 - - - 31652 RMVar_ID_31652 Human_SNP_ID_64008876 A-to-I Human chr2 - 24347954 24347954 24347954 CTCCCACCTCAGTTTCCTGAGTAGCTAGGACTATAGATGCACACCACCCATCACACCCAGCTAAT CTCCCACCTCAGTTTCCTGAGTAGCTAGGACTGTAGATGCACACCACCCATCACACCCAGCTAAT T C ITSN2 Ensembl:ENSG00000198399 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355051103 Functional Loss SNV dbSNP153 33..33 33 - - - 31653 RMVar_ID_31653 Human_SNP_ID_64008887 A-to-I Human chr2 - 24347981 24347981 24347981 ATCTCGAACTCTTGGGTTCAAGTGATCCTCCCACCTCAGTTTCCTGAGTAGCTAGGACTATAGAT ATCTCGAACTCTTGGGTTCAAGTGATCCTCCCCCCTCAGTTTCCTGAGTAGCTAGGACTATAGAT T G ITSN2 Ensembl:ENSG00000198399 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs531001482 Functional Loss SNV dbSNP153 33..33 33 - - - 31654 RMVar_ID_31654 Human_SNP_ID_64056282 A-to-I Human chr2 + 24529461 24529461 24529461 GTGATCCTCCCGCCCTGGCCTCCTGAGTAGCTAGGACTACAGGTGTGTGTCACCATACTTGGCTA GTGATCCTCCCGCCCTGGCCTCCTGAGTAGCTCGGACTACAGGTGTGTGTCACCATACTTGGCTA A C NCOA1 Ensembl:ENSG00000084676 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs770104547 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_197606,RMVar_hsa_circ_197603,RMVar_hsa_circ_197604,RMVar_hsa_circ_96912,RMVar_hsa_circ_197605 31655 RMVar_ID_31655 Human_SNP_ID_64127054 A-to-I Human chr2 + 24823510 24823510 24823510 CAGATTATTCCAGCATTTTTTTTTTTTTTTTTAAGAGTGGGTCTTGCTGTGTTTCCCAGGCTGGA CAGATTATTCCAGCATTTTTTTTTTTTTTTTTTAGAGTGGGTCTTGCTGTGTTTCCCAGGCTGGA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1345698681 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2633266,Human_RBP_ID_13831514,Human_RBP_ID_22249982,Human_RBP_ID_25527681,Human_RBP_ID_27009754,Human_RBP_ID_27288746 31656 RMVar_ID_31656 Human_SNP_ID_64127803 A-to-I Human chr2 - 24825473 24825473 24825473 AAAATTAGCCAGGCATGGTGGCCCGCACCTGTAATCCCAGCTACTTGAGAGGCTGAGGCAGGAGG AAAATTAGCCAGGCATGGTGGCCCGCACCTGTGATCCCAGCTACTTGAGAGGCTGAGGCAGGAGG T C ADCY3 Ensembl:ENSG00000138031 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs997524683 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6352,RMVar_hsa_circ_33952,RMVar_hsa_circ_93218,RMVar_hsa_circ_84336,RMVar_hsa_circ_197673,RMVar_hsa_circ_110222,RMVar_hsa_circ_197676,RMVar_hsa_circ_197675 31657 RMVar_ID_31657 Human_SNP_ID_64167836 A-to-I Human chr2 + 24979095 24979095 24979095 CGGGGCTTCGCCATCTTTCCCAGGCTGGTCTCAAACTCCTGAGCTCAAGTGACCCTCCTGCCTTG CGGGGCTTCGCCATCTTTCCCAGGCTGGTCTCGAACTCCTGAGCTCAAGTGACCCTCCTGCCTTG A G DNAJC27-AS1 Ensembl:ENSG00000224165 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1475737048 Functional Loss SNV dbSNP153 33..33 33 - - - 31658 RMVar_ID_31658 Human_SNP_ID_64274258 A-to-I Human chr2 - 25405203 25405203 25405203 GTTAGTCGGGCCAGGCATGGTAGCTCACGCCTATAATCCCAGCACTTTGAGAAGCCGAGGCAGAT GTTAGTCGGGCCAGGCATGGTAGCTCACGCCTGTAATCCCAGCACTTTGAGAAGCCGAGGCAGAT T C DTNB Ensembl:ENSG00000138101 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1217558528 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 31659 RMVar_ID_31659 Human_SNP_ID_64276809 A-to-I Human chr2 - 25415385 25415385 25415385 AAAATTAGCCAGGCATGGTAGCATGCACCCGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTAGCCAGGCATGGTAGCATGCACCCGTCGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA T G DTNB Ensembl:ENSG00000138101 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1211448248 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 31660 RMVar_ID_31660 Human_SNP_ID_64276834 A-to-I Human chr2 - 25415446 25415446 25415446 TTTTAGAAACTCTGGTCCAGCCTGGCCAACATAGTGAAACCCCATCTCTATTAAAAATACAAAAA TTTTAGAAACTCTGGTCCAGCCTGGCCAACATCGTGAAACCCCATCTCTATTAAAAATACAAAAA T G DTNB Ensembl:ENSG00000138101 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1385821948 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 31661 RMVar_ID_31661 Human_SNP_ID_64277630 A-to-I Human chr2 - 25418663 25418663 25418663 ACGGTGTCTCGCTCTGTCTCCCAGGCCAGAGTACAGTGGCATGATCTCGGCTCACTGCAACCTCC ACGGTGTCTCGCTCTGTCTCCCAGGCCAGAGTGCAGTGGCATGATCTCGGCTCACTGCAACCTCC T C DTNB Ensembl:ENSG00000138101 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991755169 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 31662 RMVar_ID_31662 Human_SNP_ID_64326614 A-to-I Human chr2 - 25627241 25627241 25627241 CGCCCAGCTAATTTTGTATTTTTAGTAGAGACAGGGTTTCTCCATGTTGGTCAGGCTGGTCTCAA CGCCCAGCTAATTTTGTATTTTTAGTAGAGACGGGGTTTCTCCATGTTGGTCAGGCTGGTCTCAA T C DTNB Ensembl:ENSG00000138101 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1277508531 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109977,RMVar_hsa_circ_15706,RMVar_hsa_circ_197718,RMVar_hsa_circ_54751,RMVar_hsa_circ_350352,RMVar_hsa_circ_350939,RMVar_hsa_circ_295016,RMVar_hsa_circ_37550,RMVar_hsa_circ_279069,RMVar_hsa_circ_197724,RMVar_hsa_circ_197725,RMVar_hsa_circ_360586,RMVar_hsa_circ_197731,RMVar_hsa_circ_334472,RMVar_hsa_circ_310555,RMVar_hsa_circ_272933,RMVar_hsa_circ_301509,RMVar_hsa_circ_318591,RMVar_hsa_circ_197732 31663 RMVar_ID_31663 Human_SNP_ID_64352882 A-to-I Human chr2 - 25732077 25732077 25732077 AAGAAATCATCCAGGCATAGTGGTGCACACCTATAGTCCCAGCTATCTGGGAGGCTAAGGCAGGA AAGAAATCATCCAGGCATAGTGGTGCACACCTGTAGTCCCAGCTATCTGGGAGGCTAAGGCAGGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334572292 Functional Loss SNV dbSNP153 33..33 33 - - - 31664 RMVar_ID_31664 Human_SNP_ID_64357887 A-to-I Human chr2 - 25751984 25751984 25751984 GCGGATCACTTGAGCCCAGGAATTCGAGACCAACTTGGGCAACATGGCAAAACCACATCTCTAAA GCGGATCACTTGAGCCCAGGAATTCGAGACCATCTTGGGCAACATGGCAAAACCACATCTCTAAA T A ASXL2 Ensembl:ENSG00000143970 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs966347452 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59815,RMVar_hsa_circ_290972,RMVar_hsa_circ_360651,RMVar_hsa_circ_63252,RMVar_hsa_circ_28564,RMVar_hsa_circ_54880,RMVar_hsa_circ_197735 31665 RMVar_ID_31665 Human_SNP_ID_64358007 A-to-I Human chr2 - 25752585 25752585 25752585 CCTCGGCCTCCCAAAGTGCTGGGATTACAGGTATGAGCCACCACTCCGAGCCAGAATACTGAGGT CCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCACTCCGAGCCAGAATACTGAGGT T C ASXL2 Ensembl:ENSG00000143970 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1469698471 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59815,RMVar_hsa_circ_290972,RMVar_hsa_circ_360651,RMVar_hsa_circ_63252,RMVar_hsa_circ_28564,RMVar_hsa_circ_54880,RMVar_hsa_circ_197735 31666 RMVar_ID_31666 Human_SNP_ID_64364115 A-to-I Human chr2 - 25777290 25777290 25777290 TCTTTAAAAGTTAGAACAAGCCTGGACAACATAGCAAGACCCCATCTTTTAAAAAAAAAACTTAA TCTTTAAAAGTTAGAACAAGCCTGGACAACATGGCAAGACCCCATCTTTTAAAAAAAAAACTTAA T C ASXL2 Ensembl:ENSG00000143970 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1051592754 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63252,RMVar_hsa_circ_54880,RMVar_hsa_circ_337696,RMVar_hsa_circ_38679,RMVar_hsa_circ_48012,RMVar_hsa_circ_338524,RMVar_hsa_circ_358129,RMVar_hsa_circ_25046,RMVar_hsa_circ_322386 31667 RMVar_ID_31667 Human_SNP_ID_64367147 A-to-I Human chr2 - 25789194 25789194 25789194 GAAGGGAGCTCAGAAAAACCCATAGCATTAATAAAAAAAATTGAACTGCAGAAAATGCAGTAATA GAAGGGAGCTCAGAAAAACCCATAGCATTAATGAAAAAAATTGAACTGCAGAAAATGCAGTAATA T C ASXL2 Ensembl:ENSG00000143970 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1244314556 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63252,RMVar_hsa_circ_54880,RMVar_hsa_circ_337696,RMVar_hsa_circ_38679,RMVar_hsa_circ_48012,RMVar_hsa_circ_338524,RMVar_hsa_circ_358129,RMVar_hsa_circ_25046,RMVar_hsa_circ_322386 31668 RMVar_ID_31668 Human_SNP_ID_64367148 A-to-I Human chr2 - 25789194 25789194 25789194 GAAGGGAGCTCAGAAAAACCCATAGCATTAATAAAAAAAATTGAACTGCAGAAAATGCAGTAATA GAAGGGAGCTCAGAAAAACCCATAGCATTAATCAAAAAAATTGAACTGCAGAAAATGCAGTAATA T G ASXL2 Ensembl:ENSG00000143970 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1244314556 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63252,RMVar_hsa_circ_54880,RMVar_hsa_circ_337696,RMVar_hsa_circ_38679,RMVar_hsa_circ_48012,RMVar_hsa_circ_338524,RMVar_hsa_circ_358129,RMVar_hsa_circ_25046,RMVar_hsa_circ_322386 31669 RMVar_ID_31669 Human_SNP_ID_64367694 A-to-I Human chr2 - 25791304 25791304 25791304 TTTTATATTTTTAGTAGAGACGGGGTTTTGCCATGTTGGCCAGACTGGTCTCGAACTCCTGACCT TTTTATATTTTTAGTAGAGACGGGGTTTTGCCGTGTTGGCCAGACTGGTCTCGAACTCCTGACCT T C ASXL2 Ensembl:ENSG00000143970 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1357489765 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63252,RMVar_hsa_circ_54880,RMVar_hsa_circ_337696,RMVar_hsa_circ_38679,RMVar_hsa_circ_48012,RMVar_hsa_circ_338524,RMVar_hsa_circ_358129,RMVar_hsa_circ_25046,RMVar_hsa_circ_322386 31670 RMVar_ID_31670 Human_SNP_ID_64368166 A-to-I Human chr2 - 25793169 25793169 25793169 GGAGTGCAGTGGCATGATCTCAGATCACTGCAACCTCGCCTCCCGGGTTCAAGCGATTCTCCTGC GGAGTGCAGTGGCATGATCTCAGATCACTGCATCCTCGCCTCCCGGGTTCAAGCGATTCTCCTGC T A ASXL2 Ensembl:ENSG00000143970 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1178718574 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63252,RMVar_hsa_circ_54880,RMVar_hsa_circ_337696,RMVar_hsa_circ_38679,RMVar_hsa_circ_48012,RMVar_hsa_circ_338524,RMVar_hsa_circ_358129,RMVar_hsa_circ_25046,RMVar_hsa_circ_322386 31671 RMVar_ID_31671 Human_SNP_ID_64387784 A-to-I Human chr2 - 25873364 25873364 25873364 ACTCTGTCGTCAGTCTGGAGAGCAGTGGTGCAATCTCGGCTCACTGCAACCTCTGCCTCCTGGGT ACTCTGTCGTCAGTCTGGAGAGCAGTGGTGCAGTCTCGGCTCACTGCAACCTCTGCCTCCTGGGT T C ASXL2 Ensembl:ENSG00000143970 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1178763103 Functional Loss SNV dbSNP153 33..33 33 - - - 31672 RMVar_ID_31672 Human_SNP_ID_64405570 A-to-I Human chr2 - 25944133 25944133 25944133 TGAGGCAGGGGAATTGCTTGAACCTGGGAGACAGAAGTTGCAGTGAGCCGAGATCATGCCATTGC TGAGGCAGGGGAATTGCTTGAACCTGGGAGACGGAAGTTGCAGTGAGCCGAGATCATGCCATTGC T C KIF3C Ensembl:ENSG00000084731 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1038505444 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_197744,RMVar_hsa_circ_294381 31673 RMVar_ID_31673 Human_SNP_ID_64405572 A-to-I Human chr2 - 25944144 25944144 25944144 ACTTGGGAGGCTGAGGCAGGGGAATTGCTTGAACCTGGGAGACAGAAGTTGCAGTGAGCCGAGAT ACTTGGGAGGCTGAGGCAGGGGAATTGCTTGACCCTGGGAGACAGAAGTTGCAGTGAGCCGAGAT T G KIF3C Ensembl:ENSG00000084731 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs995198250 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_197744,RMVar_hsa_circ_294381 31674 RMVar_ID_31674 Human_SNP_ID_64405577 A-to-I Human chr2 - 25944159 25944159 25944159 CCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGGGAATTGCTTGAACCTGGGAGACAGAAGTT CCTGTAATCCCAGCTACTTGGGAGGCTGAGGCGGGGGAATTGCTTGAACCTGGGAGACAGAAGTT T C KIF3C Ensembl:ENSG00000084731 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1325322931 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_197744,RMVar_hsa_circ_294381 31675 RMVar_ID_31675 Human_SNP_ID_64431119 A-to-I Human chr2 + 26037431 26037431 26037431 GAGGCCGAGGCAGGCGGATCACCTGAGGTCGGAAGTTCGAGACCAGCCTGATCAACATGGAGAAA GAGGCCGAGGCAGGCGGATCACCTGAGGTCGGGAGTTCGAGACCAGCCTGATCAACATGGAGAAA A G RAB10 Ensembl:ENSG00000084733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1338578179 Functional Loss SNV dbSNP153 33..33 33 - - - 31676 RMVar_ID_31676 Human_SNP_ID_64431482 A-to-I Human chr2 + 26038665 26038665 26038665 TACCATTGGGCGGGGCGCGATGGCTCACGCCTATAATCCCAGCGCTTTGGGAGGCTGAGGTGGGT TACCATTGGGCGGGGCGCGATGGCTCACGCCTGTAATCCCAGCGCTTTGGGAGGCTGAGGTGGGT A G RAB10 Ensembl:ENSG00000084733 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1429756414 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25528700 31677 RMVar_ID_31677 Human_SNP_ID_64431799 A-to-I Human chr2 + 26039803 26039803 26039803 GGCAGGCCTAGGTGGGAGGATTGCTTGGGCCCAAGAGTTCAAGACCAGCCTGGGCAACATAGTGA GGCAGGCCTAGGTGGGAGGATTGCTTGGGCCCGAGAGTTCAAGACCAGCCTGGGCAACATAGTGA A G RAB10 Ensembl:ENSG00000084733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1262419041 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22991298 31678 RMVar_ID_31678 Human_SNP_ID_64434016 A-to-I Human chr2 + 26047906 26047906 26047906 CCACCACACCCAGCTAATTTTTTTGTATTTTTAGTGGAGACGAGGTTTCACCATGTTGACCAGAC CCACCACACCCAGCTAATTTTTTTGTATTTTTCGTGGAGACGAGGTTTCACCATGTTGACCAGAC A C RAB10 Ensembl:ENSG00000084733 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1301025056 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13835428 31679 RMVar_ID_31679 Human_SNP_ID_64434286 A-to-I Human chr2 + 26048754 26048754 26048754 AAAATTAGCTGGATGTGGTGGTGTGCACCTGTAGTTTCAGCTATCTGAGAGACTGAGATGGGAGG AAAATTAGCTGGATGTGGTGGTGTGCACCTGTGGTTTCAGCTATCTGAGAGACTGAGATGGGAGG A G RAB10 Ensembl:ENSG00000084733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs986081649 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17136448 31680 RMVar_ID_31680 Human_SNP_ID_64434292 A-to-I Human chr2 + 26048769 26048769 26048769 TGGTGGTGTGCACCTGTAGTTTCAGCTATCTGAGAGACTGAGATGGGAGGATCAGCTGAGGCCAG TGGTGGTGTGCACCTGTAGTTTCAGCTATCTGGGAGACTGAGATGGGAGGATCAGCTGAGGCCAG A G RAB10 Ensembl:ENSG00000084733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs747234842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6904370,Human_RBP_ID_13835449,Human_RBP_ID_17136448,Human_RBP_ID_23864376 31681 RMVar_ID_31681 Human_SNP_ID_64434293 A-to-I Human chr2 + 26048769 26048769 26048769 TGGTGGTGTGCACCTGTAGTTTCAGCTATCTGAGAGACTGAGATGGGAGGATCAGCTGAGGCCAG TGGTGGTGTGCACCTGTAGTTTCAGCTATCTGTGAGACTGAGATGGGAGGATCAGCTGAGGCCAG A T RAB10 Ensembl:ENSG00000084733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs747234842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6904370,Human_RBP_ID_13835449,Human_RBP_ID_17136448,Human_RBP_ID_23864376 31682 RMVar_ID_31682 Human_SNP_ID_64434839 A-to-I Human chr2 + 26051121 26051121 26051121 CACTGCATCTGGTTAATTTTTAAATTTTTTGTAGAGACTGGGCCTCACTATGTTGTCCAGGCTGA CACTGCATCTGGTTAATTTTTAAATTTTTTGTGGAGACTGGGCCTCACTATGTTGTCCAGGCTGA A G RAB10 Ensembl:ENSG00000084733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1369107388 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13835523,Human_RBP_ID_23232380 31683 RMVar_ID_31683 Human_SNP_ID_64434856 A-to-I Human chr2 + 26051184 26051184 26051184 GATCTTAACTCCTGGGCTCAATTGATCCTCCTACCTTGGCCTCCCAGAGTGCTGGGATTTTAAGT GATCTTAACTCCTGGGCTCAATTGATCCTCCTGCCTTGGCCTCCCAGAGTGCTGGGATTTTAAGT A G RAB10 Ensembl:ENSG00000084733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1322047012 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13835528 31684 RMVar_ID_31684 Human_SNP_ID_64434999 A-to-I Human chr2 + 26051540 26051540 26051540 GAGGCCAAGGTGGGTGGATCACGAACGAGGTCAAGAGATCGAGACCATCCTGACCAACATGGTGA GAGGCCAAGGTGGGTGGATCACGAACGAGGTCGAGAGATCGAGACCATCCTGACCAACATGGTGA A G RAB10 Ensembl:ENSG00000084733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1486237538 Functional Loss SNV dbSNP153 33..33 33 - - - 31685 RMVar_ID_31685 Human_SNP_ID_64435035 A-to-I Human chr2 + 26051633 26051633 26051633 AAAAAAAGCCGGACGTGGTGGTGAGTGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAAAAAGCCGGACGTGGTGGTGAGTGCCTGTCGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA A C RAB10 Ensembl:ENSG00000084733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs892894855 Functional Loss SNV dbSNP153 33..33 33 - - - 31686 RMVar_ID_31686 Human_SNP_ID_64436394 A-to-I Human chr2 + 26056676 26056676 26056676 TTGAGACAGATTCTAGGTCTGTCACCCTGGCTAGAGTGTAGTGGTGTGATCATAACTCACTGTAA TTGAGACAGATTCTAGGTCTGTCACCCTGGCTGGAGTGTAGTGGTGTGATCATAACTCACTGTAA A G RAB10 Ensembl:ENSG00000084733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs961796451 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13835704 31687 RMVar_ID_31687 Human_SNP_ID_64436435 A-to-I Human chr2 + 26056837 26056837 26056837 TTTTGTAGAGGCAGAGTTTTGCAGTGTTGCCCAAGTTGGTCTCGAACTCCTGGCCTCAAGCGATC TTTTGTAGAGGCAGAGTTTTGCAGTGTTGCCCGAGTTGGTCTCGAACTCCTGGCCTCAAGCGATC A G RAB10 Ensembl:ENSG00000084733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1225996764 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13835718 31688 RMVar_ID_31688 Human_SNP_ID_64437385 A-to-I Human chr2 + 26060432 26060432 26060432 CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCTCACCACCACATCTGGCTAATTTTT CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTGCAGGCGCTCACCACCACATCTGGCTAATTTTT A G RAB10 Ensembl:ENSG00000084733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs898240687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_145833 31689 RMVar_ID_31689 Human_SNP_ID_64437695 A-to-I Human chr2 + 26061517 26061517 26061517 CCACCACAGCCGTGTTGGCTGCCCATGTAGCTAATATTACAGGTGCATGCCACCATGCCTGACTA CCACCACAGCCGTGTTGGCTGCCCATGTAGCTGATATTACAGGTGCATGCCACCATGCCTGACTA A G RAB10 Ensembl:ENSG00000084733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1286393226 Functional Loss SNV dbSNP153 33..33 33 - - - 31690 RMVar_ID_31690 Human_SNP_ID_64437992 A-to-I Human chr2 + 26062557 26062557 26062557 AAAATAAGCTGGACCTGGTGGCGCATACCTGTAATCTCAGCTACTCGGGAGGCTGAGGCACGAGA AAAATAAGCTGGACCTGGTGGCGCATACCTGTGATCTCAGCTACTCGGGAGGCTGAGGCACGAGA A G RAB10 Ensembl:ENSG00000084733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs762662934 Functional Loss SNV dbSNP153 33..33 33 - - - 31691 RMVar_ID_31691 Human_SNP_ID_64438092 A-to-I Human chr2 + 26062859 26062859 26062859 TATCTTGGCCAGGTGTGGTGGCTCATGCCTGTAATTCCAGCACTTTGGGAGGTTGCGGCAGGTGG TATCTTGGCCAGGTGTGGTGGCTCATGCCTGTGATTCCAGCACTTTGGGAGGTTGCGGCAGGTGG A G RAB10 Ensembl:ENSG00000084733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs187270086 Functional Loss SNV dbSNP153 33..33 33 - - - 31692 RMVar_ID_31692 Human_SNP_ID_64438385 A-to-I Human chr2 + 26063867 26063867 26063867 TCGCCCAGGCTGGAGTGCAGTGGCGTGACCTCAGCTCGCTGCAACCTCTGCCTCCCGGGTTCAAA TCGCCCAGGCTGGAGTGCAGTGGCGTGACCTCTGCTCGCTGCAACCTCTGCCTCCCGGGTTCAAA A T RAB10 Ensembl:ENSG00000084733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1269795748 Functional Loss SNV dbSNP153 33..33 33 - - - 31693 RMVar_ID_31693 Human_SNP_ID_64439875 A-to-I Human chr2 + 26069886 26069886 26069886 TGCCACCATGCCCCACTAATTTTTGTGTTTTTAATAGAGATGAGGTTTCGCCATGGTTGGCCAGG TGCCACCATGCCCCACTAATTTTTGTGTTTTTGATAGAGATGAGGTTTCGCCATGGTTGGCCAGG A G RAB10 Ensembl:ENSG00000084733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1233162781 Functional Loss SNV dbSNP153 33..33 33 - - - 31694 RMVar_ID_31694 Human_SNP_ID_64441608 A-to-I Human chr2 + 26076901 26076901 26076901 GGGAGGCGGAAGTTGCAGTGAGCCGAGATCACACCATTGCACTCCAGCCTGGGGGACAAGAGCGA GGGAGGCGGAAGTTGCAGTGAGCCGAGATCACGCCATTGCACTCCAGCCTGGGGGACAAGAGCGA A G RAB10 Ensembl:ENSG00000084733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992522769 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_145837,Human_RBP_ID_10006874,Human_RBP_ID_22998924,Human_RBP_ID_25587716 31695 RMVar_ID_31695 Human_SNP_ID_64443390 A-to-I Human chr2 + 26083728 26083728 26083728 TTTAGTAGAGACTGGGTTTTGCTGTGTTGGCCAGGCTGGTCTCGAACTCCTGGCCTCAAGTGATC TTTAGTAGAGACTGGGTTTTGCTGTGTTGGCCCGGCTGGTCTCGAACTCCTGGCCTCAAGTGATC A C RAB10 Ensembl:ENSG00000084733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924246872 Functional Loss SNV dbSNP153 33..33 33 - - - 31696 RMVar_ID_31696 Human_SNP_ID_64443391 A-to-I Human chr2 + 26083728 26083728 26083728 TTTAGTAGAGACTGGGTTTTGCTGTGTTGGCCAGGCTGGTCTCGAACTCCTGGCCTCAAGTGATC TTTAGTAGAGACTGGGTTTTGCTGTGTTGGCCGGGCTGGTCTCGAACTCCTGGCCTCAAGTGATC A G RAB10 Ensembl:ENSG00000084733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924246872 Functional Loss SNV dbSNP153 33..33 33 - - - 31697 RMVar_ID_31697 Human_SNP_ID_64450121 A-to-I Human chr2 + 26109121 26109121 26109121 TTTAGTAGAGATGGGGTTTCACCATGTTGGCCAAGTGTCTTGAACTCCTGACCTTAAGTGATCTA TTTAGTAGAGATGGGGTTTCACCATGTTGGCCCAGTGTCTTGAACTCCTGACCTTAAGTGATCTA A C RAB10 Ensembl:ENSG00000084733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1391163125 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57068,RMVar_hsa_circ_324091,RMVar_hsa_circ_276887,RMVar_hsa_circ_197746,RMVar_hsa_circ_197747 31698 RMVar_ID_31698 Human_SNP_ID_64450130 A-to-I Human chr2 + 26109144 26109141 26109144 ATGTTGGCCAAGTGTCTTGAACTCCTGACCTTAAGTGATCTACACGCCTCAGCCTCCCGAAGGGC ATGTTGGCCAAGTGTCTTGAACTCCTGACC___AGTGATCTACACGCCTCAGCCTCCCGAAGGGC CTTA C RAB10 Ensembl:ENSG00000084733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1466679483 Functional Loss DEL dbSNP153 31..33 33 - - - RMVar_hsa_circ_57068,RMVar_hsa_circ_324091,RMVar_hsa_circ_276887,RMVar_hsa_circ_197746,RMVar_hsa_circ_197747 31699 RMVar_ID_31699 Human_SNP_ID_64450131 A-to-I Human chr2 + 26109144 26109144 26109144 ATGTTGGCCAAGTGTCTTGAACTCCTGACCTTAAGTGATCTACACGCCTCAGCCTCCCGAAGGGC ATGTTGGCCAAGTGTCTTGAACTCCTGACCTTTAGTGATCTACACGCCTCAGCCTCCCGAAGGGC A T RAB10 Ensembl:ENSG00000084733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1198774543 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57068,RMVar_hsa_circ_324091,RMVar_hsa_circ_276887,RMVar_hsa_circ_197746,RMVar_hsa_circ_197747 31700 RMVar_ID_31700 Human_SNP_ID_64450375 A-to-I Human chr2 + 26110239 26110239 26110239 GTGCACCTGTCGTCCCAGCTACTCAAGAGTCCAAGGCAGGAGAATCTCTTGAACCTGGGAGGTAG GTGCACCTGTCGTCCCAGCTACTCAAGAGTCCCAGGCAGGAGAATCTCTTGAACCTGGGAGGTAG A C RAB10 Ensembl:ENSG00000084733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1272181109 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57068,RMVar_hsa_circ_324091,RMVar_hsa_circ_197749,RMVar_hsa_circ_92976,RMVar_hsa_circ_197746,RMVar_hsa_circ_87850,RMVar_hsa_circ_197748 31701 RMVar_ID_31701 Human_SNP_ID_64450522 A-to-I Human chr2 + 26110780 26110780 26110780 CAGGCTGGAGTGCAGTGGCACAATCTTGGCTCACTGCAATCTCTGCTTTCTGGGTTCAAGTGATT CAGGCTGGAGTGCAGTGGCACAATCTTGGCTCTCTGCAATCTCTGCTTTCTGGGTTCAAGTGATT A T RAB10 Ensembl:ENSG00000084733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1308314144 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57068,RMVar_hsa_circ_324091,RMVar_hsa_circ_197749,RMVar_hsa_circ_92976,RMVar_hsa_circ_197746,RMVar_hsa_circ_87850,RMVar_hsa_circ_197748 31702 RMVar_ID_31702 Human_SNP_ID_64450528 A-to-I Human chr2 + 26110823 26110823 26110823 TGCTTTCTGGGTTCAAGTGATTCTAGTGTCTTAGTGTCTTGAGTAGCTGGAATTACAGGTGTGCA TGCTTTCTGGGTTCAAGTGATTCTAGTGTCTTGGTGTCTTGAGTAGCTGGAATTACAGGTGTGCA A G RAB10 Ensembl:ENSG00000084733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1015602753 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13836664 RMVar_hsa_circ_57068,RMVar_hsa_circ_324091,RMVar_hsa_circ_197749,RMVar_hsa_circ_92976,RMVar_hsa_circ_197746,RMVar_hsa_circ_87850,RMVar_hsa_circ_197748 31703 RMVar_ID_31703 Human_SNP_ID_64451530 A-to-I Human chr2 + 26114847 26114847 26114847 TCACTTGAGCCCAGGAGGTCGAGGCTGCAGTGAACCATGATTGCATTACTACACTCCAGCCTGGG TCACTTGAGCCCAGGAGGTCGAGGCTGCAGTGGACCATGATTGCATTACTACACTCCAGCCTGGG A G RAB10 Ensembl:ENSG00000084733 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs999649312 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57068,RMVar_hsa_circ_324091,RMVar_hsa_circ_197749,RMVar_hsa_circ_92976,RMVar_hsa_circ_197746,RMVar_hsa_circ_87850,RMVar_hsa_circ_197748 31704 RMVar_ID_31704 Human_SNP_ID_64452801 A-to-I Human chr2 + 26119621 26119621 26119621 ACAGCTTACTGCAGCCTCTACCTCCTGAGCTCAAGCTATCCTCCCAGCCTAGCCTCCCAGGTACC ACAGCTTACTGCAGCCTCTACCTCCTGAGCTCCAGCTATCCTCCCAGCCTAGCCTCCCAGGTACC A C RAB10 Ensembl:ENSG00000084733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs143466835 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57068,RMVar_hsa_circ_324091,RMVar_hsa_circ_197749,RMVar_hsa_circ_92976,RMVar_hsa_circ_197746,RMVar_hsa_circ_87850,RMVar_hsa_circ_197748 31705 RMVar_ID_31705 Human_SNP_ID_64454486 A-to-I Human chr2 + 26126447 26126447 26126447 ACCAGAAAACTACAAAAATTAGCTGGCATGGTAGTACACACACCTGTAGTCCCAGCTACTCACAG ACCAGAAAACTACAAAAATTAGCTGGCATGGTGGTACACACACCTGTAGTCCCAGCTACTCACAG A G RAB10 Ensembl:ENSG00000084733 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs975681660 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57068,RMVar_hsa_circ_324091,RMVar_hsa_circ_197749,RMVar_hsa_circ_92976,RMVar_hsa_circ_197746,RMVar_hsa_circ_87850,RMVar_hsa_circ_197750,RMVar_hsa_circ_197748 31706 RMVar_ID_31706 Human_SNP_ID_64474963 A-to-I Human chr2 - 26206980 26206980 26206980 TTGCCCAGGCTGATCTCAAAATTCTGGCCTCAAGCAGTCCTCCTGCCTCATCCTCCCAAAGCACT TTGCCCAGGCTGATCTCAAAATTCTGGCCTCAGGCAGTCCTCCTGCCTCATCCTCCCAAAGCACT T C HADHA Ensembl:ENSG00000084754 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1329160889 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100001,RMVar_hsa_circ_58969,RMVar_hsa_circ_197761,RMVar_hsa_circ_293652,RMVar_hsa_circ_197763,RMVar_hsa_circ_37851,RMVar_hsa_circ_310789,RMVar_hsa_circ_197764 31707 RMVar_ID_31707 Human_SNP_ID_64479258 A-to-I Human chr2 - 26227753 26227753 26227753 GTCACCCAGGCTGGCCTCAGACTCCTGGGCTCAAGCAGTCTTCCTGCCTCAGCCTCCCAAGAAGC GTCACCCAGGCTGGCCTCAGACTCCTGGGCTCTAGCAGTCTTCCTGCCTCAGCCTCCCAAGAAGC T A HADHA Ensembl:ENSG00000084754 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1558327716 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569464 RMVar_hsa_circ_37851,RMVar_hsa_circ_298176,RMVar_hsa_circ_51381 31708 RMVar_ID_31708 Human_SNP_ID_64486907 A-to-I Human chr2 + 26258578 26258578 26258578 CGAGGGGTGGAAGTCAACAGCGGGTCTGCGACAGTGGCGAACAGCGGGTCTGTGACAGTGGCGAA CGAGGGGTGGAAGTCAACAGCGGGTCTGCGACGGTGGCGAACAGCGGGTCTGTGACAGTGGCGAA A G HADHB Ensembl:ENSG00000138029 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs62130462 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34037,RMVar_hsa_circ_94965,RMVar_hsa_circ_304617,RMVar_hsa_circ_72428,RMVar_hsa_circ_197769,RMVar_hsa_circ_197770 31709 RMVar_ID_31709 Human_SNP_ID_64486908 A-to-I Human chr2 + 26258578 26258578 26258578 CGAGGGGTGGAAGTCAACAGCGGGTCTGCGACAGTGGCGAACAGCGGGTCTGTGACAGTGGCGAA CGAGGGGTGGAAGTCAACAGCGGGTCTGCGACTGTGGCGAACAGCGGGTCTGTGACAGTGGCGAA A T HADHB Ensembl:ENSG00000138029 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs62130462 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34037,RMVar_hsa_circ_94965,RMVar_hsa_circ_304617,RMVar_hsa_circ_72428,RMVar_hsa_circ_197769,RMVar_hsa_circ_197770 31710 RMVar_ID_31710 Human_SNP_ID_64493621 A-to-I Human chr2 + 26285817 26285817 26285817 TGGAATGCAGTGGTAATATCTTAGCTCACTGCAACCTCCACTTCCCGGATTCAGGTGATTCTCGT TGGAATGCAGTGGTAATATCTTAGCTCACTGCTACCTCCACTTCCCGGATTCAGGTGATTCTCGT A T HADHB Ensembl:ENSG00000138029 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1477658277 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_197784,RMVar_hsa_circ_113033 31711 RMVar_ID_31711 Human_SNP_ID_64493643 A-to-I Human chr2 + 26285927 26285926 26285928 GTCCAGTTAATTTTTGTATTTTTAGTAGAGACAGAGTTTCGCCATGTTGGCCAGGCTAGTCTCGA GTCCAGTTAATTTTTGTATTTTTAGTAGAGAC__AGTTTCGCCATGTTGGCCAGGCTAGTCTCGA CAG C HADHB Ensembl:ENSG00000138029 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1402794447 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_197784,RMVar_hsa_circ_113033 31712 RMVar_ID_31712 Human_SNP_ID_64493914 A-to-I Human chr2 + 26286997 26286997 26286997 AGGTTGAGGCGGGTAGGTCACTTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAAC AGGTTGAGGCGGGTAGGTCACTTGAGGTCAGGGGTTCGAGACCAGCCTGGCCAACATGGTGAAAC A G HADHB Ensembl:ENSG00000138029 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1387621165 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_197784,RMVar_hsa_circ_113033 31713 RMVar_ID_31713 Human_SNP_ID_64511303 A-to-I Human chr2 + 26355888 26355888 26355888 TTCAACCTCTCAAGTAGCTGGACTACAGTCATACGCCACCACACCTGGCTCATTTTTGTATTATT TTCAACCTCTCAAGTAGCTGGACTACAGTCATTCGCCACCACACCTGGCTCATTTTTGTATTATT A T SELENOI Ensembl:ENSG00000138018 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1242281146 Functional Loss SNV dbSNP153 33..33 33 - - - 31714 RMVar_ID_31714 Human_SNP_ID_64511751 A-to-I Human chr2 + 26357883 26357883 26357883 CCCATAATTCCCACGAATTGTGGGAGGGACCCATTCGGAGAAATTGAACCATGGGGGCGGTTTCC CCCATAATTCCCACGAATTGTGGGAGGGACCCGTTCGGAGAAATTGAACCATGGGGGCGGTTTCC A G SELENOI Ensembl:ENSG00000138018 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11884137 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_3508,GWAS_ID_3509,GWAS_ID_3510,GWAS_ID_3511,GWAS_ID_3512,GWAS_ID_3513 31715 RMVar_ID_31715 Human_SNP_ID_64512577 A-to-I Human chr2 + 26361753 26361753 26361753 TTGGCTCACTGCAGCCTGTGCCCCCTTGGTTCAAACGATTCTCCTGCCTCAGCCTCCCAAGTACC TTGGCTCACTGCAGCCTGTGCCCCCTTGGTTCTAACGATTCTCCTGCCTCAGCCTCCCAAGTACC A T SELENOI Ensembl:ENSG00000138018 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs998354860 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18758160 31716 RMVar_ID_31716 Human_SNP_ID_64620501 A-to-I Human chr2 + 26778961 26778960 26778962 AGCATTATATTTTCTTTTTTTTTTTTTGAGACAGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCA AGCATTATATTTTCTTTTTTTTTTTTTGAGAC__AGTCTCGCTCTGTCGCCCAGGCTGGAGTGCA CAG C CENPA,SLC35F6 Ensembl:ENSG00000115163,Ensembl:ENSG00000213699 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947019381 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_548311,Human_RBP_ID_6905427 31717 RMVar_ID_31717 Human_SNP_ID_64620503 A-to-I Human chr2 + 26778961 26778961 26778961 AGCATTATATTTTCTTTTTTTTTTTTTGAGACAGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCA AGCATTATATTTTCTTTTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCA A G CENPA,SLC35F6 Ensembl:ENSG00000115163,Ensembl:ENSG00000213699 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049410547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_548311,Human_RBP_ID_6905427 31718 RMVar_ID_31718 Human_SNP_ID_64620558 A-to-I Human chr2 + 26779129 26779129 26779129 CTGGGTAACTTTTATAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTCCTGACCT CTGGGTAACTTTTATAGAGATGGGGTTTCACCGTGTTGGCCAGGCTGGTCTCAAACTCCTGACCT A G CENPA,SLC35F6 Ensembl:ENSG00000115163,Ensembl:ENSG00000213699 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037646206 Functional Loss SNV dbSNP153 33..33 33 - - - 31719 RMVar_ID_31719 Human_SNP_ID_64620779 A-to-I Human chr2 + 26780004 26780004 26780004 ATTGTTTTATTTTTTTGGCAGAGATGGGTCTCACTGTGTTGCCCAGGCTGATCTCAAACTCCTGG ATTGTTTTATTTTTTTGGCAGAGATGGGTCTCGCTGTGTTGCCCAGGCTGATCTCAAACTCCTGG A G CENPA,SLC35F6 Ensembl:ENSG00000115163,Ensembl:ENSG00000213699 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1490944494 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244028,Human_RBP_ID_548324,Human_RBP_ID_777600,Human_RBP_ID_6905460,Human_RBP_ID_8200467,Human_RBP_ID_13839251,Human_RBP_ID_17506994,Human_RBP_ID_17954651,Human_RBP_ID_26486277,Human_RBP_ID_27479265,Human_RBP_ID_27694632 Human_miRNA_ID_162062,Human_miRNA_ID_1081037 31720 RMVar_ID_31720 Human_SNP_ID_64621403 A-to-I Human chr2 + 26782610 26782609 26782611 ATTGAAGAAGGAAAATTTTTCTTTTTAGAGACAGAGTCTTGATCTGTTGCTGTCACTGGGGTGCA ATTGAAGAAGGAAAATTTTTCTTTTTAGAGAC__AGTCTTGATCTGTTGCTGTCACTGGGGTGCA CAG C CENPA Ensembl:ENSG00000115163 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs967012179 Functional Loss DEL dbSNP153 33..34 33 - - - 31721 RMVar_ID_31721 Human_SNP_ID_64621409 A-to-I Human chr2 + 26782648 26782648 26782648 TTGATCTGTTGCTGTCACTGGGGTGCAGTGGCATGATCCTATCTCACTGTAGCCTTAAACTCCTG TTGATCTGTTGCTGTCACTGGGGTGCAGTGGCCTGATCCTATCTCACTGTAGCCTTAAACTCCTG A C CENPA Ensembl:ENSG00000115163 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1398443885 Functional Loss SNV dbSNP153 33..33 33 - - - 31722 RMVar_ID_31722 Human_SNP_ID_64621452 A-to-I Human chr2 + 26782822 26782822 26782822 GTTGCCCAGACTGATCTCGAACTACTGGGCTCAAACAATGCTCCTGCCTTGGCCTTCCAAAATTT GTTGCCCAGACTGATCTCGAACTACTGGGCTCGAACAATGCTCCTGCCTTGGCCTTCCAAAATTT A G CENPA Ensembl:ENSG00000115163 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1427609330 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13839308 31723 RMVar_ID_31723 Human_SNP_ID_64622002 A-to-I Human chr2 + 26784547 26784547 26784547 ATGATTTCGGCTCACTGCAACCTCCGCCTTTCAGGTTCAAGCAACTCTGCCTCAGCCTCCTGAGT ATGATTTCGGCTCACTGCAACCTCCGCCTTTCGGGTTCAAGCAACTCTGCCTCAGCCTCCTGAGT A G CENPA Ensembl:ENSG00000115163 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348041479 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13839314 31724 RMVar_ID_31724 Human_SNP_ID_64622082 A-to-I Human chr2 + 26784838 26784838 26784838 CGAACAACTTGGCCTCCCAAAGCGCTGGGATTACAGGCATGAACCACCGCACCCCAGCCCAGCAT CGAACAACTTGGCCTCCCAAAGCGCTGGGATTGCAGGCATGAACCACCGCACCCCAGCCCAGCAT A G CENPA Ensembl:ENSG00000115163 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs951949105 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13839321 31725 RMVar_ID_31725 Human_SNP_ID_64622083 A-to-I Human chr2 + 26784844 26784844 26784844 ACTTGGCCTCCCAAAGCGCTGGGATTACAGGCATGAACCACCGCACCCCAGCCCAGCATTTGTCC ACTTGGCCTCCCAAAGCGCTGGGATTACAGGCGTGAACCACCGCACCCCAGCCCAGCATTTGTCC A G CENPA Ensembl:ENSG00000115163 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1320054768 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13839321 31726 RMVar_ID_31726 Human_SNP_ID_64660464 A-to-I Human chr2 + 26936807 26936807 26936807 GTCTCTACTAAAAATACAAAAATTAGCTGGGCATGGTGGCTCGTGCCTGTAATCCCAGCTACTCC GTCTCTACTAAAAATACAAAAATTAGCTGGGCGTGGTGGCTCGTGCCTGTAATCCCAGCTACTCC A G DPYSL5 Ensembl:ENSG00000157851 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1250687316 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82245,RMVar_hsa_circ_197821,RMVar_hsa_circ_266170,RMVar_hsa_circ_323130,RMVar_hsa_circ_197824,RMVar_hsa_circ_37223,RMVar_hsa_circ_197828,RMVar_hsa_circ_88280,RMVar_hsa_circ_304630,RMVar_hsa_circ_344414,RMVar_hsa_circ_331395,RMVar_hsa_circ_197827,RMVar_hsa_circ_275059,RMVar_hsa_circ_197830,RMVar_hsa_circ_197831 31727 RMVar_ID_31727 Human_SNP_ID_64684508 A-to-I Human chr2 + 27041335 27041335 27041335 GGGCTTCCAGAAGAATATAGCACCGCATTGGGAAACAGCAGCCTCACCTCCACCTGAAGCCTGGG GGGCTTCCAGAAGAATATAGCACCGCATTGGGCAACAGCAGCCTCACCTCCACCTGAAGCCTGGG A C TMEM214 Ensembl:ENSG00000119777 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs529905061 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17279606,Human_RBP_ID_26486291 Human_miRNA_ID_2712493,Human_miRNA_ID_3048475 RMVar_hsa_circ_107517,RMVar_hsa_circ_197840,RMVar_hsa_circ_76788,RMVar_hsa_circ_197846,RMVar_hsa_circ_113408,RMVar_hsa_circ_122109,RMVar_hsa_circ_197847,RMVar_hsa_circ_266054,RMVar_hsa_circ_197848,RMVar_hsa_circ_103260,RMVar_hsa_circ_197851,RMVar_hsa_circ_197856,RMVar_hsa_circ_110063,RMVar_hsa_circ_85702,RMVar_hsa_circ_197859,RMVar_hsa_circ_75837,RMVar_hsa_circ_128031,RMVar_hsa_circ_197862,RMVar_hsa_circ_84935,RMVar_hsa_circ_197863,RMVar_hsa_circ_88723,RMVar_hsa_circ_197864,RMVar_hsa_circ_83193,RMVar_hsa_circ_197865,RMVar_hsa_circ_197866 31728 RMVar_ID_31728 Human_SNP_ID_64691776 A-to-I Human chr2 - 27066131 27066131 27066131 CTCCTGCATCCCAAGTAGCTGGGACAACAGGCACACGCCACCAAGCCCAGCTAATTTTTAAATTT CTCCTGCATCCCAAGTAGCTGGGACAACAGGCGCACGCCACCAAGCCCAGCTAATTTTTAAATTT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1234028550 Functional Loss SNV dbSNP153 33..33 33 - - - 31729 RMVar_ID_31729 Human_SNP_ID_64691787 A-to-I Human chr2 - 27066174 27066174 27066174 GCTGTAGTGCAGTGGCATGAACATGGCTCACTACAAACTTGACCTCCTGCATCCCAAGTAGCTGG GCTGTAGTGCAGTGGCATGAACATGGCTCACTGCAAACTTGACCTCCTGCATCCCAAGTAGCTGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1396482650 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13840502 31730 RMVar_ID_31730 Human_SNP_ID_64691799 A-to-I Human chr2 - 27066212 27066212 27066212 TTTTTTTTTTGGAGACAGGGTCTCACTCTGTCACCTAGGCTGTAGTGCAGTGGCATGAACATGGC TTTTTTTTTTGGAGACAGGGTCTCACTCTGTCGCCTAGGCTGTAGTGCAGTGGCATGAACATGGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1257948891 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13840502 31731 RMVar_ID_31731 Human_SNP_ID_64692251 A-to-I Human chr2 + 27067657 27067657 27067657 CCTGATTCATTCAACATACCAGGTCTGTACCCACTGCCACTGAAATCTGGGTTTGCCAGCCTCCT CCTGATTCATTCAACATACCAGGTCTGTACCCCCTGCCACTGAAATCTGGGTTTGCCAGCCTCCT A C AGBL5 Ensembl:ENSG00000084693 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11681145 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_3514,GWAS_ID_3515,GWAS_ID_3516,GWAS_ID_3517,GWAS_ID_3518,GWAS_ID_3519,GWAS_ID_3520 RMVar_hsa_circ_84980,RMVar_hsa_circ_197868 31732 RMVar_ID_31732 Human_SNP_ID_64692252 A-to-I Human chr2 + 27067657 27067657 27067657 CCTGATTCATTCAACATACCAGGTCTGTACCCACTGCCACTGAAATCTGGGTTTGCCAGCCTCCT CCTGATTCATTCAACATACCAGGTCTGTACCCGCTGCCACTGAAATCTGGGTTTGCCAGCCTCCT A G AGBL5 Ensembl:ENSG00000084693 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11681145 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - GWAS_ID_3514,GWAS_ID_3515,GWAS_ID_3516,GWAS_ID_3517,GWAS_ID_3518,GWAS_ID_3519,GWAS_ID_3520 RMVar_hsa_circ_84980,RMVar_hsa_circ_197868 31733 RMVar_ID_31733 Human_SNP_ID_64728186 A-to-I Human chr2 - 27200173 27200173 27200173 AGGCTCGTAGGGAGCAGGATCATGCCAGAAATAGGGATGGAAGTGCATCCTCTGGGAAAAAGATA AGGCTCGTAGGGAGCAGGATCATGCCAGAAATGGGGATGGAAGTGCATCCTCTGGGAAAAAGATA T C SLC5A6 Ensembl:ENSG00000138074 Protein coding exon GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1167559077 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4631973,Human_RBP_ID_8202049,Human_RBP_ID_17509609,Human_RBP_ID_17965894,Human_RBP_ID_20559065,Human_RBP_ID_22815308,Human_RBP_ID_27010205,Human_RBP_ID_27289169 Human_Splice_Rec_227363 Human_miRNA_ID_444858,Human_miRNA_ID_2465634,Human_miRNA_ID_2465635 RMVar_hsa_circ_78423,RMVar_hsa_circ_106739,RMVar_hsa_circ_112154,RMVar_hsa_circ_119087,RMVar_hsa_circ_121555,RMVar_hsa_circ_126405,RMVar_hsa_circ_114734,RMVar_hsa_circ_109663,RMVar_hsa_circ_97454,RMVar_hsa_circ_98021,RMVar_hsa_circ_87706,RMVar_hsa_circ_197893,RMVar_hsa_circ_197897,RMVar_hsa_circ_197899,RMVar_hsa_circ_197901,RMVar_hsa_circ_197903,RMVar_hsa_circ_75931,RMVar_hsa_circ_197902,RMVar_hsa_circ_197900,RMVar_hsa_circ_197898,RMVar_hsa_circ_197895,RMVar_hsa_circ_197896,RMVar_hsa_circ_197894,RMVar_hsa_circ_4315,RMVar_hsa_circ_197892,RMVar_hsa_circ_353100 31734 RMVar_ID_31734 Human_SNP_ID_64730763 A-to-I Human chr2 - 27208545 27208545 27208545 TTTGGCTGGTCCCTTTGCCTCTCAGCTCCGTGACTGGGTTGCTTCTCTCCAGAATGGAGAATCGT TTTGGCTGGTCCCTTTGCCTCTCAGCTCCGTGTCTGGGTTGCTTCTCTCCAGAATGGAGAATCGT T A SLC5A6 Ensembl:ENSG00000138074 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1275529 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2135560,Human_miRNA_ID_2664357,Human_miRNA_ID_2791493 RMVar_hsa_circ_106739,RMVar_hsa_circ_197892,RMVar_hsa_circ_353100,RMVar_hsa_circ_51227,RMVar_hsa_circ_361520,RMVar_hsa_circ_197905,RMVar_hsa_circ_374398,RMVar_hsa_circ_81906,RMVar_hsa_circ_197914,RMVar_hsa_circ_63631,RMVar_hsa_circ_197915,RMVar_hsa_circ_348807 31735 RMVar_ID_31735 Human_SNP_ID_64730764 A-to-I Human chr2 - 27208545 27208545 27208545 TTTGGCTGGTCCCTTTGCCTCTCAGCTCCGTGACTGGGTTGCTTCTCTCCAGAATGGAGAATCGT TTTGGCTGGTCCCTTTGCCTCTCAGCTCCGTGGCTGGGTTGCTTCTCTCCAGAATGGAGAATCGT T C SLC5A6 Ensembl:ENSG00000138074 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1275529 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2135560,Human_miRNA_ID_2664357,Human_miRNA_ID_2791493 RMVar_hsa_circ_106739,RMVar_hsa_circ_197892,RMVar_hsa_circ_353100,RMVar_hsa_circ_51227,RMVar_hsa_circ_361520,RMVar_hsa_circ_197905,RMVar_hsa_circ_374398,RMVar_hsa_circ_81906,RMVar_hsa_circ_197914,RMVar_hsa_circ_63631,RMVar_hsa_circ_197915,RMVar_hsa_circ_348807 31736 RMVar_ID_31736 Human_SNP_ID_64737605 A-to-I Human chr2 + 27229405 27229405 27229405 TCTCCCACCCCATCCTTCTGAGGAGTGAGACTACAGGTGTACACCACCACACCTTGCTAATTTTT TCTCCCACCCCATCCTTCTGAGGAGTGAGACTGCAGGTGTACACCACCACACCTTGCTAATTTTT A G CAD Ensembl:ENSG00000084774 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1290392674 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13841255 RMVar_hsa_circ_103567,RMVar_hsa_circ_197925,RMVar_hsa_circ_99013,RMVar_hsa_circ_197928,RMVar_hsa_circ_11796,RMVar_hsa_circ_108530,RMVar_hsa_circ_75864,RMVar_hsa_circ_86177,RMVar_hsa_circ_122633,RMVar_hsa_circ_371456,RMVar_hsa_circ_197930,RMVar_hsa_circ_197932,RMVar_hsa_circ_197931,RMVar_hsa_circ_197929,RMVar_hsa_circ_378699,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_38451,RMVar_hsa_circ_30423,RMVar_hsa_circ_122142,RMVar_hsa_circ_197947 31737 RMVar_ID_31737 Human_SNP_ID_64737869 A-to-I Human chr2 + 27230177 27230177 27230177 GGAGAATCACTTGAACCCAGGAGGCACAGGTTACACTGAGCTGAGATCATGCCATTGCAGTCCAG GGAGAATCACTTGAACCCAGGAGGCACAGGTTGCACTGAGCTGAGATCATGCCATTGCAGTCCAG A G CAD Ensembl:ENSG00000084774 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1194531851 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25530129 RMVar_hsa_circ_103567,RMVar_hsa_circ_197925,RMVar_hsa_circ_99013,RMVar_hsa_circ_197928,RMVar_hsa_circ_11796,RMVar_hsa_circ_108530,RMVar_hsa_circ_75864,RMVar_hsa_circ_86177,RMVar_hsa_circ_122633,RMVar_hsa_circ_371456,RMVar_hsa_circ_197930,RMVar_hsa_circ_197932,RMVar_hsa_circ_197931,RMVar_hsa_circ_197929,RMVar_hsa_circ_378699,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_38451,RMVar_hsa_circ_30423,RMVar_hsa_circ_122142,RMVar_hsa_circ_197947 31738 RMVar_ID_31738 Human_SNP_ID_64737966 A-to-I Human chr2 + 27230515 27230515 27230515 AGACATGGTGACACGCACCTGTAATCACAGCTACTCAGGAGGCTGAGGCAGGAGAATCTCTTGAA AGACATGGTGACACGCACCTGTAATCACAGCTGCTCAGGAGGCTGAGGCAGGAGAATCTCTTGAA A G CAD Ensembl:ENSG00000084774 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1001538950 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103567,RMVar_hsa_circ_197925,RMVar_hsa_circ_99013,RMVar_hsa_circ_197928,RMVar_hsa_circ_11796,RMVar_hsa_circ_108530,RMVar_hsa_circ_75864,RMVar_hsa_circ_86177,RMVar_hsa_circ_122633,RMVar_hsa_circ_371456,RMVar_hsa_circ_197930,RMVar_hsa_circ_197932,RMVar_hsa_circ_197931,RMVar_hsa_circ_197929,RMVar_hsa_circ_378699,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_38451,RMVar_hsa_circ_30423,RMVar_hsa_circ_122142,RMVar_hsa_circ_197947 31739 RMVar_ID_31739 Human_SNP_ID_64746747 A-to-I Human chr2 - 27259628 27259628 27259628 TAGATGAGAGCCGGGTGCGGTGGCTCACACCTATAATCCCAGCAACTCAGTAGGCTGAGGTAGGA TAGATGAGAGCCGGGTGCGGTGGCTCACACCTGTAATCCCAGCAACTCAGTAGGCTGAGGTAGGA T C SLC30A3 Ensembl:ENSG00000115194 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1418734340 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98403,RMVar_hsa_circ_197972 31740 RMVar_ID_31740 Human_SNP_ID_64761220 A-to-I Human chr2 - 27313931 27313931 27313931 GAGGTGAGCAGATCACCTGAGGTCAGGGGTTCAAGATCAGCCTGGCTAACATGGCAAAACCCCAT GAGGTGAGCAGATCACCTGAGGTCAGGGGTTCGAGATCAGCCTGGCTAACATGGCAAAACCCCAT T C MPV17 Ensembl:ENSG00000115204 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs897410294 Functional Loss SNV dbSNP153 33..33 33 - - - 31741 RMVar_ID_31741 Human_SNP_ID_64761299 A-to-I Human chr2 - 27314284 27314284 27314284 GGGTCTTGTTCTGTCGCCCAGGCAGCAGTGTAATGGCGTGATCACTGCAGCCTGGACCTCCTGGG GGGTCTTGTTCTGTCGCCCAGGCAGCAGTGTAGTGGCGTGATCACTGCAGCCTGGACCTCCTGGG T C MPV17 Ensembl:ENSG00000115204 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1049597725 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22991492 31742 RMVar_ID_31742 Human_SNP_ID_64762485 A-to-I Human chr2 - 27319355 27319355 27319355 CCATGCCCAGCTAATTTCTTTTGTTTTTTGGTAGAGATGGGGTTTTGCCATATTGCCCAAGCTTT CCATGCCCAGCTAATTTCTTTTGTTTTTTGGTGGAGATGGGGTTTTGCCATATTGCCCAAGCTTT T C MPV17 Ensembl:ENSG00000115204 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1469185517 Functional Loss SNV dbSNP153 33..33 33 - - - 31743 RMVar_ID_31743 Human_SNP_ID_64762637 A-to-I Human chr2 - 27319994 27319994 27319994 TGACCTCGTGATTCACCCGCCTCGGCCTCCTAAAGTGCTGGGGTTACAGGTGTGAGCCACTGAGC TGACCTCGTGATTCACCCGCCTCGGCCTCCTAGAGTGCTGGGGTTACAGGTGTGAGCCACTGAGC T C MPV17 Ensembl:ENSG00000115204 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1412621703 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25530363 31744 RMVar_ID_31744 Human_SNP_ID_64762654 A-to-I Human chr2 - 27320053 27320053 27320053 TTTTCTATTTTTAGTAGAGACGGGATTTCACCATGTTGGCCAGGCTGGTCTCGGACACTTGACCT TTTTCTATTTTTAGTAGAGACGGGATTTCACCGTGTTGGCCAGGCTGGTCTCGGACACTTGACCT T C MPV17 Ensembl:ENSG00000115204 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs944604680 Functional Loss SNV dbSNP153 33..33 33 - - - 31745 RMVar_ID_31745 Human_SNP_ID_64762794 A-to-I Human chr2 - 27320563 27320563 27320563 TTGGGACGCCGAGGTGGGCAGATCACGAGGTCAGGAGATCGAGACCAACCTGGCTAACACGGTGA TTGGGACGCCGAGGTGGGCAGATCACGAGGTCGGGAGATCGAGACCAACCTGGCTAACACGGTGA T C MPV17 Ensembl:ENSG00000115204 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs911654843 Functional Loss SNV dbSNP153 33..33 33 - - - 31746 RMVar_ID_31746 Human_SNP_ID_64767927 A-to-I Human chr2 - 27338661 27338661 27338661 GTAGTGGGGTGTGCCTGTAGTCCCAGCTACTCAGGAGGCAGAGGTGAGAGGATTGCTTGAGCCCA GTAGTGGGGTGTGCCTGTAGTCCCAGCTACTCGGGAGGCAGAGGTGAGAGGATTGCTTGAGCCCA T C GTF3C2 Ensembl:ENSG00000115207 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs779489282 Functional Loss SNV dbSNP153 33..33 33 - - - 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 31747 RMVar_ID_31747 Human_SNP_ID_64769578 A-to-I Human chr2 - 27344314 27344314 27344314 ATTTAATAAATGGAAGCTTTATGGCCAGGCGCAGTGACTCATTATCTGTAATCCCAGCACTTTGG ATTTAATAAATGGAAGCTTTATGGCCAGGCGCGGTGACTCATTATCTGTAATCCCAGCACTTTGG T C GTF3C2 Ensembl:ENSG00000115207 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs770876159 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103493,RMVar_hsa_circ_197976,RMVar_hsa_circ_25458,RMVar_hsa_circ_197986,RMVar_hsa_circ_128167,RMVar_hsa_circ_364979,RMVar_hsa_circ_368158 31748 RMVar_ID_31748 Human_SNP_ID_64769687 A-to-I Human chr2 - 27344721 27344721 27344721 CCTTGGCCTCTCAAAGTGTTGGAATTACAGGCATGAGCCATCCTGCCTGGCCTTTTACTTATTCT CCTTGGCCTCTCAAAGTGTTGGAATTACAGGCGTGAGCCATCCTGCCTGGCCTTTTACTTATTCT T C GTF3C2 Ensembl:ENSG00000115207 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs940270496 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103493,RMVar_hsa_circ_197976,RMVar_hsa_circ_25458,RMVar_hsa_circ_197986,RMVar_hsa_circ_128167,RMVar_hsa_circ_364979,RMVar_hsa_circ_368158 31749 RMVar_ID_31749 Human_SNP_ID_64769710 A-to-I Human chr2 - 27344801 27344801 27344801 TTTAAAATTTTTTGTAGAGATGAGGTCTCCCTATGTTGCCCAGACTGGTCTTGAACTCCTGGCCT TTTAAAATTTTTTGTAGAGATGAGGTCTCCCTCTGTTGCCCAGACTGGTCTTGAACTCCTGGCCT T G GTF3C2 Ensembl:ENSG00000115207 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs549371692 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103493,RMVar_hsa_circ_197976,RMVar_hsa_circ_25458,RMVar_hsa_circ_197986,RMVar_hsa_circ_128167,RMVar_hsa_circ_364979,RMVar_hsa_circ_368158 31750 RMVar_ID_31750 Human_SNP_ID_64769737 A-to-I Human chr2 - 27344877 27344877 27344877 AGGCTCAAGCAATCCTCCTGTCTCAGCCTTCCAAGTAGCTGGGACTACAGGTGCGCACCACCATG AGGCTCAAGCAATCCTCCTGTCTCAGCCTTCCTAGTAGCTGGGACTACAGGTGCGCACCACCATG T A GTF3C2 Ensembl:ENSG00000115207 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs928414493 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25530479 RMVar_hsa_circ_103493,RMVar_hsa_circ_197976,RMVar_hsa_circ_25458,RMVar_hsa_circ_197986,RMVar_hsa_circ_128167,RMVar_hsa_circ_364979,RMVar_hsa_circ_368158 31751 RMVar_ID_31751 Human_SNP_ID_64769744 A-to-I Human chr2 - 27344898 27344898 27344898 TCACTGTAACCTCGAACTCCTAGGCTCAAGCAATCCTCCTGTCTCAGCCTTCCAAGTAGCTGGGA TCACTGTAACCTCGAACTCCTAGGCTCAAGCAGTCCTCCTGTCTCAGCCTTCCAAGTAGCTGGGA T C GTF3C2 Ensembl:ENSG00000115207 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1374987998 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103493,RMVar_hsa_circ_197976,RMVar_hsa_circ_25458,RMVar_hsa_circ_197986,RMVar_hsa_circ_128167,RMVar_hsa_circ_364979,RMVar_hsa_circ_368158 31752 RMVar_ID_31752 Human_SNP_ID_64769794 A-to-I Human chr2 - 27345159 27345159 27345159 CTCAAGGAGCCTCCCAAGTCTTCAGCCTCCCAAGTAGCTGAGACTACAGGTGTGCACCACCATGT CTCAAGGAGCCTCCCAAGTCTTCAGCCTCCCAGGTAGCTGAGACTACAGGTGTGCACCACCATGT T C GTF3C2 Ensembl:ENSG00000115207 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs190431522 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103493,RMVar_hsa_circ_197976,RMVar_hsa_circ_25458,RMVar_hsa_circ_197986,RMVar_hsa_circ_128167,RMVar_hsa_circ_364979,RMVar_hsa_circ_368158 31753 RMVar_ID_31753 Human_SNP_ID_64769795 A-to-I Human chr2 - 27345160 27345160 27345160 GCTCAAGGAGCCTCCCAAGTCTTCAGCCTCCCAAGTAGCTGAGACTACAGGTGTGCACCACCATG GCTCAAGGAGCCTCCCAAGTCTTCAGCCTCCCGAGTAGCTGAGACTACAGGTGTGCACCACCATG T C GTF3C2 Ensembl:ENSG00000115207 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1317709188 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103493,RMVar_hsa_circ_197976,RMVar_hsa_circ_25458,RMVar_hsa_circ_197986,RMVar_hsa_circ_128167,RMVar_hsa_circ_364979,RMVar_hsa_circ_368158 31754 RMVar_ID_31754 Human_SNP_ID_64769864 A-to-I Human chr2 - 27345510 27345510 27345510 CGGCTCGCTGCAACCTCCACCCCACGGGTTCAATTGATTCTCTTGCCTCCGCCTCCTGAGTAGCT CGGCTCGCTGCAACCTCCACCCCACGGGTTCAGTTGATTCTCTTGCCTCCGCCTCCTGAGTAGCT T C GTF3C2 Ensembl:ENSG00000115207 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1281183871 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103493,RMVar_hsa_circ_197976,RMVar_hsa_circ_25458,RMVar_hsa_circ_197986,RMVar_hsa_circ_128167,RMVar_hsa_circ_364979,RMVar_hsa_circ_368158 31755 RMVar_ID_31755 Human_SNP_ID_64769981 A-to-I Human chr2 - 27345888 27345888 27345888 CAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTTAGCTGGGTGTGGTGGCGGGCACC CAACATGGTGAAACCCCATCTCTACTAAAAATTCAAAAATTTAGCTGGGTGTGGTGGCGGGCACC T A GTF3C2 Ensembl:ENSG00000115207 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1279447342 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25530494 RMVar_hsa_circ_103493,RMVar_hsa_circ_197976,RMVar_hsa_circ_25458,RMVar_hsa_circ_197986,RMVar_hsa_circ_128167,RMVar_hsa_circ_364979,RMVar_hsa_circ_368158 31756 RMVar_ID_31756 Human_SNP_ID_64770062 A-to-I Human chr2 - 27346162 27346162 27346162 AAAATTAGCCAGGCATGGTGATACATGCCTATAGTCCTAGCTACTTGGGAGGCTGAGGCAGGAGG AAAATTAGCCAGGCATGGTGATACATGCCTATCGTCCTAGCTACTTGGGAGGCTGAGGCAGGAGG T G GTF3C2 Ensembl:ENSG00000115207 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs564670481 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103493,RMVar_hsa_circ_197976,RMVar_hsa_circ_25458,RMVar_hsa_circ_197986,RMVar_hsa_circ_128167,RMVar_hsa_circ_364979,RMVar_hsa_circ_368158 31757 RMVar_ID_31757 Human_SNP_ID_64770063 A-to-I Human chr2 - 27346164 27346164 27346164 TAAAAATTAGCCAGGCATGGTGATACATGCCTATAGTCCTAGCTACTTGGGAGGCTGAGGCAGGA TAAAAATTAGCCAGGCATGGTGATACATGCCTGTAGTCCTAGCTACTTGGGAGGCTGAGGCAGGA T C GTF3C2 Ensembl:ENSG00000115207 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1471136352 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103493,RMVar_hsa_circ_197976,RMVar_hsa_circ_25458,RMVar_hsa_circ_197986,RMVar_hsa_circ_128167,RMVar_hsa_circ_364979,RMVar_hsa_circ_368158 31758 RMVar_ID_31758 Human_SNP_ID_64770176 A-to-I Human chr2 - 27346483 27346483 27346483 GTCAGGCATGGTGGTGCATGCCTGTAGTCCCAACTACTCAGGCGGCTGAGGTGGGAGGATCACTT GTCAGGCATGGTGGTGCATGCCTGTAGTCCCAGCTACTCAGGCGGCTGAGGTGGGAGGATCACTT T C GTF3C2 Ensembl:ENSG00000115207 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1019938876 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103493,RMVar_hsa_circ_197976,RMVar_hsa_circ_25458,RMVar_hsa_circ_197986,RMVar_hsa_circ_128167,RMVar_hsa_circ_364979,RMVar_hsa_circ_368158 31759 RMVar_ID_31759 Human_SNP_ID_64770290 A-to-I Human chr2 - 27346919 27346919 27346919 GGCCAAGGTGGGAGGATCTCTTGAGGTTAGGAATTCAAGACAAGCCTGGGCAAAATAGCAAGACC GGCCAAGGTGGGAGGATCTCTTGAGGTTAGGAGTTCAAGACAAGCCTGGGCAAAATAGCAAGACC T C GTF3C2 Ensembl:ENSG00000115207 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1231304904 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569242,Human_RBP_ID_25530511 RMVar_hsa_circ_103493,RMVar_hsa_circ_197976,RMVar_hsa_circ_25458,RMVar_hsa_circ_197986,RMVar_hsa_circ_128167,RMVar_hsa_circ_364979,RMVar_hsa_circ_368158 31760 RMVar_ID_31760 Human_SNP_ID_64770719 A-to-I Human chr2 - 27348556 27348556 27348556 CAAGCAATCTGCTTGCTTCGGCCTCCCAACATACTGGGAATACAGGCATGAGCCTGTACCTGGTC CAAGCAATCTGCTTGCTTCGGCCTCCCAACATGCTGGGAATACAGGCATGAGCCTGTACCTGGTC T C GTF3C2 Ensembl:ENSG00000115207 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs559459460 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103493,RMVar_hsa_circ_197976,RMVar_hsa_circ_25458,RMVar_hsa_circ_197986,RMVar_hsa_circ_128167,RMVar_hsa_circ_364979,RMVar_hsa_circ_368158 31761 RMVar_ID_31761 Human_SNP_ID_64770762 A-to-I Human chr2 - 27348788 27348788 27348788 AACCAAATCTTTATTATTTTTTCTTTTGAGATAGCATCTTGCTCTGTCTGCCCAGGCTGGGATGC AACCAAATCTTTATTATTTTTTCTTTTGAGATGGCATCTTGCTCTGTCTGCCCAGGCTGGGATGC T C GTF3C2 Ensembl:ENSG00000115207 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs992030832 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569243 RMVar_hsa_circ_103493,RMVar_hsa_circ_197976,RMVar_hsa_circ_25458,RMVar_hsa_circ_197986,RMVar_hsa_circ_128167,RMVar_hsa_circ_364979,RMVar_hsa_circ_368158 31762 RMVar_ID_31762 Human_SNP_ID_64772117 A-to-I Human chr2 - 27353603 27353603 27353603 GAAATCCCATCTCTACTAAAAGTACAAAACTTAGCTGGGCATGGTGGCACATGCCTGTAATCCCA GAAATCCCATCTCTACTAAAAGTACAAAACTTCGCTGGGCATGGTGGCACATGCCTGTAATCCCA T G GTF3C2 Ensembl:ENSG00000115207 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1034483476 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_197986,RMVar_hsa_circ_128167 31763 RMVar_ID_31763 Human_SNP_ID_64772152 A-to-I Human chr2 - 27353780 27353780 27353780 GAGGTCAAGGTGCAGTGAGCCATGATCATCGCACTACTGCATTCCAGCCTGGGTGACAGGGGAAA GAGGTCAAGGTGCAGTGAGCCATGATCATCGCCCTACTGCATTCCAGCCTGGGTGACAGGGGAAA T G GTF3C2 Ensembl:ENSG00000115207 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs925909157 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13842336,Human_RBP_ID_23182573 RMVar_hsa_circ_197986,RMVar_hsa_circ_128167 31764 RMVar_ID_31764 Human_SNP_ID_64772399 A-to-I Human chr2 - 27354672 27354672 27354672 ACTGCAACCTCTCCCTCTGCCTCTTGGGTTCAAGTGATTCTCCTGTCTCAGCCTCCCGAGTAGAT ACTGCAACCTCTCCCTCTGCCTCTTGGGTTCACGTGATTCTCCTGTCTCAGCCTCCCGAGTAGAT T G GTF3C2 Ensembl:ENSG00000115207 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs767006313 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25530584 RMVar_hsa_circ_197986,RMVar_hsa_circ_128167 31765 RMVar_ID_31765 Human_SNP_ID_64774526 A-to-I Human chr2 + 27360466 27360462 27360466 AAGGTTTTGTTTGTTTTTTGAGACTGAGTCTCACTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCG AAGGTTTTGTTTGTTTTTTGAGACTGAGT____CTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCG TCTCA T AC074117.1 Ensembl:ENSG00000234072 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1306553628 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_3621904 31766 RMVar_ID_31766 Human_SNP_ID_64774528 A-to-I Human chr2 + 27360466 27360466 27360466 AAGGTTTTGTTTGTTTTTTGAGACTGAGTCTCACTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCG AAGGTTTTGTTTGTTTTTTGAGACTGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCG A G AC074117.1 Ensembl:ENSG00000234072 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1000167943 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3621904 31767 RMVar_ID_31767 Human_SNP_ID_64785817 A-to-I Human chr2 - 27393888 27393888 27393888 GTCTTGGCAGGCACCTGTAGTCCCAGGTACTCAGGAGTTTTGAGACGGGAGAATGGCGTGAACCC GTCTTGGCAGGCACCTGTAGTCCCAGGTACTCGGGAGTTTTGAGACGGGAGAATGGCGTGAACCC T C PPM1G Ensembl:ENSG00000115241 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs914650103 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78831,RMVar_hsa_circ_198005,RMVar_hsa_circ_127075,RMVar_hsa_circ_198017 31768 RMVar_ID_31768 Human_SNP_ID_64786723 A-to-I Human chr2 - 27397141 27397141 27397141 ATTGTGGCTGGGCATGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGGGGCCAAGACGGGTGAA ATTGTGGCTGGGCATGGTGGCTCACGCCTGTAGTCCCAGCACTTTGGGGGGCCAAGACGGGTGAA T C PPM1G Ensembl:ENSG00000115241 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1377754844 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78831,RMVar_hsa_circ_198005,RMVar_hsa_circ_127075,RMVar_hsa_circ_198017 31769 RMVar_ID_31769 Human_SNP_ID_64787348 A-to-I Human chr2 - 27399501 27399499 27399501 CCCAGCTAATTTTTTGTATTTCTAGTAGAGACAGGGCATTACCATGTTGTTCAGGCTGGTGTCGA CCCAGCTAATTTTTTGTATTTCTAGTAGAGAC__GGCATTACCATGTTGTTCAGGCTGGTGTCGA CCT C PPM1G Ensembl:ENSG00000115241 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1322823560 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_2635066,Human_RBP_ID_13843050 RMVar_hsa_circ_78831,RMVar_hsa_circ_198005,RMVar_hsa_circ_127075,RMVar_hsa_circ_198017 31770 RMVar_ID_31770 Human_SNP_ID_64788593 A-to-I Human chr2 - 27404688 27404688 27404688 CGCCCGCCTCGGCCTCCCAAAGTGCTGGCATTACAGGCGTGAGCCACCATGCCTGGCCCATCAGT CGCCCGCCTCGGCCTCCCAAAGTGCTGGCATTGCAGGCGTGAGCCACCATGCCTGGCCCATCAGT T C PPM1G Ensembl:ENSG00000115241 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1215777885 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78831,RMVar_hsa_circ_198005,RMVar_hsa_circ_127075,RMVar_hsa_circ_198017 31771 RMVar_ID_31771 Human_SNP_ID_64788882 A-to-I Human chr2 - 27405605 27405605 27405605 CAGATCACCTGAGGTCAGTTCGAGACCAGCCTAGTCAACATGGTGAAACCCCGTCTCTACTGAAA CAGATCACCTGAGGTCAGTTCGAGACCAGCCTGGTCAACATGGTGAAACCCCGTCTCTACTGAAA T C PPM1G Ensembl:ENSG00000115241 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs962259769 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78831,RMVar_hsa_circ_198005,RMVar_hsa_circ_127075,RMVar_hsa_circ_198017 31772 RMVar_ID_31772 Human_SNP_ID_64789275 A-to-I Human chr2 - 27407106 27407106 27407106 AAAAAATTAGCTGAATGTGGTGGTGCGTGCCTATAATCATAGCTACTTGGAAGGCTGAGGCAGGA AAAAAATTAGCTGAATGTGGTGGTGCGTGCCTGTAATCATAGCTACTTGGAAGGCTGAGGCAGGA T C PPM1G Ensembl:ENSG00000115241 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1486170955 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78831,RMVar_hsa_circ_198005,RMVar_hsa_circ_127075,RMVar_hsa_circ_198017 31773 RMVar_ID_31773 Human_SNP_ID_64789511 A-to-I Human chr2 - 27407947 27407947 27407947 CGCCTCCCAGGTTCGAGCAATTCTCCTGCCTCAGCCTCCCTAGTAGTTGGGATTACAGGCATGTG CGCCTCCCAGGTTCGAGCAATTCTCCTGCCTCCGCCTCCCTAGTAGTTGGGATTACAGGCATGTG T G PPM1G Ensembl:ENSG00000115241 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1216714041 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78831,RMVar_hsa_circ_198005,RMVar_hsa_circ_127075,RMVar_hsa_circ_198017 31774 RMVar_ID_31774 Human_SNP_ID_64802670 A-to-I Human chr2 - 27454192 27454191 27454193 TCTCCCACTATTGGGGCCTCAGTCCTATACTCAGTCTCTCCTCTGTCCCCACCTGGAGGCAGGTT TCTCCCACTATTGGGGCCTCAGTCCTATACT__GTCTCTCCTCTGTCCCCACCTGGAGGCAGGTT CTG C IFT172 Ensembl:ENSG00000138002 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs918776652 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_22668910 RMVar_hsa_circ_92608,RMVar_hsa_circ_198038,RMVar_hsa_circ_266381 31775 RMVar_ID_31775 Human_SNP_ID_64803089 A-to-I Human chr2 - 27455792 27455792 27455792 GCTGTCTTGCTTCTTCATGGTCCATGATGCCAACTGAGGTTGTCAGTACAATAAAACCAAACTGG GCTGTCTTGCTTCTTCATGGTCCATGATGCCAGCTGAGGTTGTCAGTACAATAAAACCAAACTGG T C IFT172 Ensembl:ENSG00000138002 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1052834415 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92608,RMVar_hsa_circ_198038,RMVar_hsa_circ_266381,RMVar_hsa_circ_76966,RMVar_hsa_circ_198041 31776 RMVar_ID_31776 Human_SNP_ID_64803090 A-to-I Human chr2 - 27455792 27455792 27455792 GCTGTCTTGCTTCTTCATGGTCCATGATGCCAACTGAGGTTGTCAGTACAATAAAACCAAACTGG GCTGTCTTGCTTCTTCATGGTCCATGATGCCACCTGAGGTTGTCAGTACAATAAAACCAAACTGG T G IFT172 Ensembl:ENSG00000138002 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1052834415 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92608,RMVar_hsa_circ_198038,RMVar_hsa_circ_266381,RMVar_hsa_circ_76966,RMVar_hsa_circ_198041 31777 RMVar_ID_31777 Human_SNP_ID_64806313 A-to-I Human chr2 - 27468077 27468077 27468077 TGGTTTACTGCAACCTCTTCCTCCCGGGTTTAAGCAATTCTCCTGCCTCAGCCTCCTAAGTAGCT TGGTTTACTGCAACCTCTTCCTCCCGGGTTTATGCAATTCTCCTGCCTCAGCCTCCTAAGTAGCT T A IFT172 Ensembl:ENSG00000138002 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1268356994 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92608,RMVar_hsa_circ_198038,RMVar_hsa_circ_266381,RMVar_hsa_circ_21207,RMVar_hsa_circ_93165,RMVar_hsa_circ_198042,RMVar_hsa_circ_58041,RMVar_hsa_circ_198043,RMVar_hsa_circ_109736,RMVar_hsa_circ_69316,RMVar_hsa_circ_274215 31778 RMVar_ID_31778 Human_SNP_ID_64837482 A-to-I Human chr2 + 27591438 27591438 27591438 GTTCTTAAAATTATTATTATTATTATTTTGAGACAGAGTCTCGCTCTGTCACCAGGCTGGAGCAC GTTCTTAAAATTATTATTATTATTATTTTGAGGCAGAGTCTCGCTCTGTCACCAGGCTGGAGCAC A G ZNF512,AC074091.2 Ensembl:ENSG00000243943,Ensembl:ENSG00000259080 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs756859976 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_30724,RMVar_hsa_circ_86354,RMVar_hsa_circ_50835,RMVar_hsa_circ_198053 31779 RMVar_ID_31779 Human_SNP_ID_64837564 A-to-I Human chr2 + 27591743 27591743 27591743 AAAATTATTTTTTGTAGAGACAAGGTCTTGCTATGTTGCCCAGGCTGGTCTTGAACTCATGGGCT AAAATTATTTTTTGTAGAGACAAGGTCTTGCTGTGTTGCCCAGGCTGGTCTTGAACTCATGGGCT A G ZNF512,AC074091.2 Ensembl:ENSG00000243943,Ensembl:ENSG00000259080 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1286322088 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_30724,RMVar_hsa_circ_86354,RMVar_hsa_circ_50835,RMVar_hsa_circ_198053 31780 RMVar_ID_31780 Human_SNP_ID_64838095 A-to-I Human chr2 + 27593481 27593481 27593481 TCTCTATGAAAAAACACAAAAATTTAGTGGGTATGATGGTGTGCACCTGTGGTTCCAGCTACTCG TCTCTATGAAAAAACACAAAAATTTAGTGGGTGTGATGGTGTGCACCTGTGGTTCCAGCTACTCG A G ZNF512,AC074091.2 Ensembl:ENSG00000243943,Ensembl:ENSG00000259080 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs943732812 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13844240,Human_RBP_ID_23865680,Human_RBP_ID_25531251 RMVar_hsa_circ_30724,RMVar_hsa_circ_86354,RMVar_hsa_circ_50835,RMVar_hsa_circ_198053 31781 RMVar_ID_31781 Human_SNP_ID_64839582 A-to-I Human chr2 + 27598932 27598932 27598932 CAGGCTCACCGCACCCTCCTTCTCCTGGGTTCAAGCGATTCTCCTGCCTCAGCTTGTAATGCCAG CAGGCTCACCGCACCCTCCTTCTCCTGGGTTCGAGCGATTCTCCTGCCTCAGCTTGTAATGCCAG A G ZNF512,AC074091.2 Ensembl:ENSG00000243943,Ensembl:ENSG00000259080 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1038138192 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_30724,RMVar_hsa_circ_86354,RMVar_hsa_circ_50835,RMVar_hsa_circ_198054,RMVar_hsa_circ_91131,RMVar_hsa_circ_321901,RMVar_hsa_circ_198053,RMVar_hsa_circ_339727,RMVar_hsa_circ_273369,RMVar_hsa_circ_198055,RMVar_hsa_circ_198056,RMVar_hsa_circ_198059,RMVar_hsa_circ_198058,RMVar_hsa_circ_84847,RMVar_hsa_circ_297883,RMVar_hsa_circ_198057 31782 RMVar_ID_31782 Human_SNP_ID_64841091 A-to-I Human chr2 + 27604660 27604659 27604660 AAAATAAGCCAGGCATGGTGGTGTACACCTGTAGTCCCAAGTACTTGGGAAACTGAGGTGGGAGG AAAATAAGCCAGGCATGGTGGTGTACACCTGT_GTCCCAAGTACTTGGGAAACTGAGGTGGGAGG TA T ZNF512,AC074091.2 Ensembl:ENSG00000243943,Ensembl:ENSG00000259080 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1276291271 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_86354,RMVar_hsa_circ_50835,RMVar_hsa_circ_321901,RMVar_hsa_circ_198053,RMVar_hsa_circ_339727,RMVar_hsa_circ_273369,RMVar_hsa_circ_198055,RMVar_hsa_circ_198056,RMVar_hsa_circ_198059,RMVar_hsa_circ_198058,RMVar_hsa_circ_297883,RMVar_hsa_circ_369107,RMVar_hsa_circ_277043,RMVar_hsa_circ_361613,RMVar_hsa_circ_198062,RMVar_hsa_circ_198063,RMVar_hsa_circ_47675 31783 RMVar_ID_31783 Human_SNP_ID_64850839 A-to-I Human chr2 + 27644059 27644040 27644060 AAAATTAGCTGGGCGTGGTCGTGCATGTCTGTAATTCCAGCTACTCGCTGAGGCTGGAGAGTCTC AAAATTAGCTGGGC____________________TTCCAGCTACTCGCTGAGGCTGGAGAGTCTC CGTGGTCGTGCATGTCTGTAA C GPN1 Ensembl:ENSG00000198522 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1308449412 Functional Loss DEL dbSNP153 15..34 33 - - - RMVar_hsa_circ_100710,RMVar_hsa_circ_119954,RMVar_hsa_circ_198069,RMVar_hsa_circ_198076,RMVar_hsa_circ_111039,RMVar_hsa_circ_198070,RMVar_hsa_circ_198071,RMVar_hsa_circ_198074,RMVar_hsa_circ_99533,RMVar_hsa_circ_120886,RMVar_hsa_circ_198079,RMVar_hsa_circ_198077,RMVar_hsa_circ_320379,RMVar_hsa_circ_297935 31784 RMVar_ID_31784 Human_SNP_ID_64851118 A-to-I Human chr2 + 27645101 27645101 27645101 GCATTCCCCCTGTCTCAGCCTCCAGAGTAGCTAGATCTACAGGTGTGTGCCACCACGTCTGGCTA GCATTCCCCCTGTCTCAGCCTCCAGAGTAGCTGGATCTACAGGTGTGTGCCACCACGTCTGGCTA A G GPN1 Ensembl:ENSG00000198522 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1424553242 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100710,RMVar_hsa_circ_119954,RMVar_hsa_circ_198069,RMVar_hsa_circ_198076,RMVar_hsa_circ_111039,RMVar_hsa_circ_198070,RMVar_hsa_circ_198071,RMVar_hsa_circ_198074,RMVar_hsa_circ_99533,RMVar_hsa_circ_120886,RMVar_hsa_circ_198079,RMVar_hsa_circ_198077,RMVar_hsa_circ_320379,RMVar_hsa_circ_297935 31785 RMVar_ID_31785 Human_SNP_ID_64852075 A-to-I Human chr2 + 27649165 27649165 27649165 TACTTGGGAGGCTGAGGCAGGAGGACTGCTTGAACCTGGGAGGCGGAGGCTGCAGTGAACTGAGA TACTTGGGAGGCTGAGGCAGGAGGACTGCTTGTACCTGGGAGGCGGAGGCTGCAGTGAACTGAGA A T GPN1 Ensembl:ENSG00000198522 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1411054648 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119954,RMVar_hsa_circ_198069,RMVar_hsa_circ_198076,RMVar_hsa_circ_111039,RMVar_hsa_circ_198071,RMVar_hsa_circ_198074,RMVar_hsa_circ_99533,RMVar_hsa_circ_120886 31786 RMVar_ID_31786 Human_SNP_ID_64914668 A-to-I Human chr2 + 27923857 27923857 27923857 AGCCAAGTGTGGTGGCATGTGCCTGTGGTCCCAGCTACCTGGGAGGCTGATGTGGGAGGATCGCC AGCCAAGTGTGGTGGCATGTGCCTGTGGTCCCGGCTACCTGGGAGGCTGATGTGGGAGGATCGCC A G MRPL33,BABAM2 Ensembl:ENSG00000243147,Ensembl:ENSG00000158019 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350829024 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1740,RMVar_hsa_circ_81798,RMVar_hsa_circ_72708,RMVar_hsa_circ_83972,RMVar_hsa_circ_198089,RMVar_hsa_circ_198090,RMVar_hsa_circ_337088,RMVar_hsa_circ_37430,RMVar_hsa_circ_292787,RMVar_hsa_circ_198092,RMVar_hsa_circ_198093 31787 RMVar_ID_31787 Human_SNP_ID_64930413 A-to-I Human chr2 + 27995854 27995854 27995854 TGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCACCTGGCCCCTCATG TGCCCACCTCGGCCTCCCAAAGTGCTGGGATTCCAGGCGTGAGCCACTGCACCTGGCCCCTCATG A C BABAM2 Ensembl:ENSG00000158019 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1207849274 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13012,RMVar_hsa_circ_1740,RMVar_hsa_circ_83972,RMVar_hsa_circ_198090,RMVar_hsa_circ_39738,RMVar_hsa_circ_321137,RMVar_hsa_circ_341655,RMVar_hsa_circ_49983 31788 RMVar_ID_31788 Human_SNP_ID_64974016 A-to-I Human chr2 + 28187851 28187851 28187851 CCACCACGCCCGGTTTATTTTTTGTTTTTAGTAGAGACTGAGTTTCACCATGTTGGTCAGACTGG CCACCACGCCCGGTTTATTTTTTGTTTTTAGTGGAGACTGAGTTTCACCATGTTGGTCAGACTGG A G BABAM2 Ensembl:ENSG00000158019 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs767300291 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17133,RMVar_hsa_circ_83972,RMVar_hsa_circ_198090,RMVar_hsa_circ_15931,RMVar_hsa_circ_350707,RMVar_hsa_circ_49597,RMVar_hsa_circ_56631,RMVar_hsa_circ_67343 31789 RMVar_ID_31789 Human_SNP_ID_65026415 A-to-I Human chr2 + 28411062 28411062 28411062 CTCAGCTACTCGGGAGGCTGAGACTGGAGAATAGCTTGAACCCGGGAGGCAGAGGCTGCAGTGAG CTCAGCTACTCGGGAGGCTGAGACTGGAGAATGGCTTGAACCCGGGAGGCAGAGGCTGCAGTGAG A G FOSL2 Ensembl:ENSG00000075426 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1409128051 Functional Loss SNV dbSNP153 33..33 33 - - - 31790 RMVar_ID_31790 Human_SNP_ID_65029033 A-to-I Human chr2 + 28421607 28421607 28421607 TTTTATTTATTTTTGAGATGGAGTCTCGCTCTATTGTTTGGGTAGAGTGCAGCGGCACAATCTTG TTTTATTTATTTTTGAGATGGAGTCTCGCTCTGTTGTTTGGGTAGAGTGCAGCGGCACAATCTTG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041046505 Functional Loss SNV dbSNP153 33..33 33 - - - 31791 RMVar_ID_31791 Human_SNP_ID_65029219 A-to-I Human chr2 + 28422482 28422480 28422482 ACGGTGGCTCACACCTGTAATCCCAGCACTTCAGGAGGCCCAAGGCAGGTGGATCACTTGAGGCC ACGGTGGCTCACACCTGTAATCCCAGCACTT__GGAGGCCCAAGGCAGGTGGATCACTTGAGGCC TCA T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1236154611 Functional Loss DEL dbSNP153 32..33 33 - - - 31792 RMVar_ID_31792 Human_SNP_ID_65029245 A-to-I Human chr2 + 28422560 28422560 28422560 CAGCCTGGGTAACACGACAAGACCTCGTCTCTATAAAAACTTAAAAAATTAGCTGGGCATGGTTG CAGCCTGGGTAACACGACAAGACCTCGTCTCTGTAAAAACTTAAAAAATTAGCTGGGCATGGTTG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs896895839 Functional Loss SNV dbSNP153 33..33 33 - - - 31793 RMVar_ID_31793 Human_SNP_ID_65115311 A-to-I Human chr2 + 28755157 28755157 28755157 TGCAACCTCTGCCCCTGCAGGTCCAAGCGATTATTCTGCCTCAGCTTCCCAAGTAGCTGGGACTA TGCAACCTCTGCCCCTGCAGGTCCAAGCGATTCTTCTGCCTCAGCTTCCCAAGTAGCTGGGACTA A C PPP1CB Ensembl:ENSG00000213639 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1443603057 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_198107,RMVar_hsa_circ_270896,RMVar_hsa_circ_342271,RMVar_hsa_circ_198108 31794 RMVar_ID_31794 Human_SNP_ID_65117726 A-to-I Human chr2 + 28764326 28764326 28764326 ACTTAAAATACAAAAAATTAGCTGGGCATAGTAGCACCCACCTATAATCCCAGCTACTCGGGAGG ACTTAAAATACAAAAAATTAGCTGGGCATAGTGGCACCCACCTATAATCCCAGCTACTCGGGAGG A G PPP1CB Ensembl:ENSG00000213639 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1359880795 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_198107,RMVar_hsa_circ_270896,RMVar_hsa_circ_342271,RMVar_hsa_circ_198108 31795 RMVar_ID_31795 Human_SNP_ID_65123511 A-to-I Human chr2 + 28786207 28786207 28786207 CTGATCTCGGCTCACTGCAACCTCCACCTCCCAGGTTCAAGCAGTTCTCTTGCTTCAGCCTCCCA CTGATCTCGGCTCACTGCAACCTCCACCTCCCGGGTTCAAGCAGTTCTCTTGCTTCAGCCTCCCA A G SPDYA,PPP1CB Ensembl:ENSG00000163806,Ensembl:ENSG00000213639 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1328802428 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_198112,RMVar_hsa_circ_198107,RMVar_hsa_circ_342271,RMVar_hsa_circ_198108,RMVar_hsa_circ_112730,RMVar_hsa_circ_273853,RMVar_hsa_circ_273465,RMVar_hsa_circ_198113,RMVar_hsa_circ_52550,RMVar_hsa_circ_198111,RMVar_hsa_circ_198117,RMVar_hsa_circ_112573,RMVar_hsa_circ_198114,RMVar_hsa_circ_275815,RMVar_hsa_circ_375294,RMVar_hsa_circ_198119,RMVar_hsa_circ_78730,RMVar_hsa_circ_198118,RMVar_hsa_circ_198116 31796 RMVar_ID_31796 Human_SNP_ID_65124435 A-to-I Human chr2 + 28789249 28789249 28789249 TATTTTGGGGCTGGGCATGGTGGCTCACATCTATAATCCCAGCACTTTGGCAAGCTGAGATGGGT TATTTTGGGGCTGGGCATGGTGGCTCACATCTGTAATCCCAGCACTTTGGCAAGCTGAGATGGGT A G SPDYA,PPP1CB Ensembl:ENSG00000163806,Ensembl:ENSG00000213639 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956782836 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_198112,RMVar_hsa_circ_198107,RMVar_hsa_circ_342271,RMVar_hsa_circ_198108,RMVar_hsa_circ_112730,RMVar_hsa_circ_273465,RMVar_hsa_circ_198113,RMVar_hsa_circ_52550,RMVar_hsa_circ_198111,RMVar_hsa_circ_198117,RMVar_hsa_circ_112573,RMVar_hsa_circ_198114,RMVar_hsa_circ_375294,RMVar_hsa_circ_78730,RMVar_hsa_circ_198118,RMVar_hsa_circ_198116 31797 RMVar_ID_31797 Human_SNP_ID_65124475 A-to-I Human chr2 + 28789398 28789398 28789398 GGGTGTGGTGGTGCGTGCCTGTGGTCCCAGCTACGTGGGAGGCTGAGGTGGGAGGATCGCTTGAG GGGTGTGGTGGTGCGTGCCTGTGGTCCCAGCTTCGTGGGAGGCTGAGGTGGGAGGATCGCTTGAG A T SPDYA,PPP1CB Ensembl:ENSG00000163806,Ensembl:ENSG00000213639 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs949137783 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_198112,RMVar_hsa_circ_198107,RMVar_hsa_circ_342271,RMVar_hsa_circ_198108,RMVar_hsa_circ_112730,RMVar_hsa_circ_273465,RMVar_hsa_circ_198113,RMVar_hsa_circ_52550,RMVar_hsa_circ_198111,RMVar_hsa_circ_198117,RMVar_hsa_circ_112573,RMVar_hsa_circ_198114,RMVar_hsa_circ_375294,RMVar_hsa_circ_78730,RMVar_hsa_circ_198118,RMVar_hsa_circ_198116 31798 RMVar_ID_31798 Human_SNP_ID_65124484 A-to-I Human chr2 + 28789429 28789429 28789429 TACGTGGGAGGCTGAGGTGGGAGGATCGCTTGAGCCTAGGAGATCAAGGCTGCAGTGAGCCATGT TACGTGGGAGGCTGAGGTGGGAGGATCGCTTGCGCCTAGGAGATCAAGGCTGCAGTGAGCCATGT A C SPDYA,PPP1CB Ensembl:ENSG00000163806,Ensembl:ENSG00000213639 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1046858412 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_198112,RMVar_hsa_circ_198107,RMVar_hsa_circ_342271,RMVar_hsa_circ_198108,RMVar_hsa_circ_112730,RMVar_hsa_circ_273465,RMVar_hsa_circ_198113,RMVar_hsa_circ_52550,RMVar_hsa_circ_198111,RMVar_hsa_circ_198117,RMVar_hsa_circ_112573,RMVar_hsa_circ_198114,RMVar_hsa_circ_375294,RMVar_hsa_circ_78730,RMVar_hsa_circ_198118,RMVar_hsa_circ_198116 31799 RMVar_ID_31799 Human_SNP_ID_65124595 A-to-I Human chr2 + 28789808 28789808 28789808 TTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGCCCTTGAACTCCTGAGCTCAAGTGATC TTTAGTAGAGACAGGGTTTCACCATGTTGGCCGGGCTGCCCTTGAACTCCTGAGCTCAAGTGATC A G SPDYA,PPP1CB Ensembl:ENSG00000163806,Ensembl:ENSG00000213639 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs890895174 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8517000,Human_RBP_ID_13849790 RMVar_hsa_circ_198112,RMVar_hsa_circ_198107,RMVar_hsa_circ_342271,RMVar_hsa_circ_198108,RMVar_hsa_circ_112730,RMVar_hsa_circ_273465,RMVar_hsa_circ_198113,RMVar_hsa_circ_52550,RMVar_hsa_circ_198111,RMVar_hsa_circ_198117,RMVar_hsa_circ_112573,RMVar_hsa_circ_198114,RMVar_hsa_circ_375294,RMVar_hsa_circ_78730,RMVar_hsa_circ_198118,RMVar_hsa_circ_198116 31800 RMVar_ID_31800 Human_SNP_ID_65124666 A-to-I Human chr2 + 28790139 28790139 28790139 CTCTGTCTCCACAGAAGATACAAAACAGCCAGATGTGGTGGTGTGCACCTGTAGTCCCAGCTTGC CTCTGTCTCCACAGAAGATACAAAACAGCCAGGTGTGGTGGTGTGCACCTGTAGTCCCAGCTTGC A G SPDYA,PPP1CB Ensembl:ENSG00000163806,Ensembl:ENSG00000213639 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7608105 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_3521,GWAS_ID_3522,GWAS_ID_3523,GWAS_ID_3524,GWAS_ID_3525,GWAS_ID_3526,GWAS_ID_3527,GWAS_ID_3528,GWAS_ID_3529,GWAS_ID_3530,GWAS_ID_3531,GWAS_ID_3532,GWAS_ID_3533,GWAS_ID_3534,GWAS_ID_3535,GWAS_ID_3536,GWAS_ID_3537,GWAS_ID_3538,GWAS_ID_3539,GWAS_ID_3540,GWAS_ID_3541,GWAS_ID_3542,GWAS_ID_3543,GWAS_ID_3544,GWAS_ID_3545,GWAS_ID_3546,GWAS_ID_3547,GWAS_ID_3548,GWAS_ID_3549,GWAS_ID_3550,GWAS_ID_3551,GWAS_ID_3552,GWAS_ID_3553,GWAS_ID_3554,GWAS_ID_3555,GWAS_ID_3556,GWAS_ID_3557 RMVar_hsa_circ_198112,RMVar_hsa_circ_198107,RMVar_hsa_circ_342271,RMVar_hsa_circ_198108,RMVar_hsa_circ_112730,RMVar_hsa_circ_273465,RMVar_hsa_circ_198113,RMVar_hsa_circ_52550,RMVar_hsa_circ_198111,RMVar_hsa_circ_198117,RMVar_hsa_circ_112573,RMVar_hsa_circ_198114,RMVar_hsa_circ_375294,RMVar_hsa_circ_78730,RMVar_hsa_circ_198118,RMVar_hsa_circ_198116 31801 RMVar_ID_31801 Human_SNP_ID_65124672 A-to-I Human chr2 + 28790159 28790159 28790159 CAAAACAGCCAGATGTGGTGGTGTGCACCTGTAGTCCCAGCTTGCTTGGGAGGCTGTGGCAGGAA CAAAACAGCCAGATGTGGTGGTGTGCACCTGTCGTCCCAGCTTGCTTGGGAGGCTGTGGCAGGAA A C SPDYA,PPP1CB Ensembl:ENSG00000163806,Ensembl:ENSG00000213639 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1472003827 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_198112,RMVar_hsa_circ_198107,RMVar_hsa_circ_342271,RMVar_hsa_circ_198108,RMVar_hsa_circ_112730,RMVar_hsa_circ_273465,RMVar_hsa_circ_198113,RMVar_hsa_circ_52550,RMVar_hsa_circ_198111,RMVar_hsa_circ_198117,RMVar_hsa_circ_112573,RMVar_hsa_circ_198114,RMVar_hsa_circ_375294,RMVar_hsa_circ_78730,RMVar_hsa_circ_198118,RMVar_hsa_circ_198116 31802 RMVar_ID_31802 Human_SNP_ID_65125267 A-to-I Human chr2 + 28792447 28792447 28792447 GGAGGCTGAGGTGGGAAGATCTCTTGAGCCCCAGGAAGTTGTGACTGCAGTAAGCCAAGATTGCA GGAGGCTGAGGTGGGAAGATCTCTTGAGCCCCTGGAAGTTGTGACTGCAGTAAGCCAAGATTGCA A T SPDYA,PPP1CB Ensembl:ENSG00000163806,Ensembl:ENSG00000213639 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs562565674 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13849808 RMVar_hsa_circ_198112,RMVar_hsa_circ_198107,RMVar_hsa_circ_342271,RMVar_hsa_circ_198108,RMVar_hsa_circ_112730,RMVar_hsa_circ_273465,RMVar_hsa_circ_198113,RMVar_hsa_circ_52550,RMVar_hsa_circ_198111,RMVar_hsa_circ_198117,RMVar_hsa_circ_112573,RMVar_hsa_circ_198114,RMVar_hsa_circ_375294,RMVar_hsa_circ_78730,RMVar_hsa_circ_198118,RMVar_hsa_circ_198116 31803 RMVar_ID_31803 Human_SNP_ID_65137342 A-to-I Human chr2 + 28840250 28840250 28840250 CTGTTCATCACAGTGGAGCTGTCAGAAACTACAACAGAGATGAAGTTCAGCTGCCCCGGGGACCT CTGTTCATCACAGTGGAGCTGTCAGAAACTACGACAGAGATGAAGTTCAGCTGCCCCGGGGACCT A G SPDYA Ensembl:ENSG00000163806 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1318416758 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_231028,Human_Splice_Rec_231038,Human_Splice_Rec_231042,Human_Splice_Rec_231056 RMVar_hsa_circ_107971,RMVar_hsa_circ_198122 31804 RMVar_ID_31804 Human_SNP_ID_65138433 A-to-I Human chr2 - 28845188 28845188 28845188 CCAGCTACTCAGGAGGCTGAGGTGGGAGGATCACTTGAACAGAGGAGGTTGAGGCTACAGTGAGC CCAGCTACTCAGGAGGCTGAGGTGGGAGGATCTCTTGAACAGAGGAGGTTGAGGCTACAGTGAGC T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749741557 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14020403 RMVar_hsa_circ_198123 31805 RMVar_ID_31805 Human_SNP_ID_65140439 A-to-I Human chr2 - 28852837 28852837 28852837 CTCCCACCTCAGCTTCCTGAATAGCTGGTACTACGGGCTTGTGCCACTGCATCCAGCTACTTTTT CTCCCACCTCAGCTTCCTGAATAGCTGGTACTGCGGGCTTGTGCCACTGCATCCAGCTACTTTTT T C TRMT61B Ensembl:ENSG00000171103 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1032727064 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_282561,RMVar_hsa_circ_271089,RMVar_hsa_circ_198127,RMVar_hsa_circ_198128,RMVar_hsa_circ_366187 31806 RMVar_ID_31806 Human_SNP_ID_65140643 A-to-I Human chr2 - 28853714 28853714 28853714 GTCCTGCCTCAGCCTTCCCAGTAGCTGGGACTATAGGTGTGCACCACCACACCTGGCTAATTTTT GTCCTGCCTCAGCCTTCCCAGTAGCTGGGACTGTAGGTGTGCACCACCACACCTGGCTAATTTTT T C TRMT61B Ensembl:ENSG00000171103 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1207513340 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_282561,RMVar_hsa_circ_271089,RMVar_hsa_circ_198127,RMVar_hsa_circ_198128,RMVar_hsa_circ_366187 31807 RMVar_ID_31807 Human_SNP_ID_65141148 A-to-I Human chr2 - 28855710 28855710 28855710 CCCGCCTCGGCCTCCCAAACTGCTTGGATTACAGGTGTGAGCCACCATGCCTGGCCTTGACTTGG CCCGCCTCGGCCTCCCAAACTGCTTGGATTACGGGTGTGAGCCACCATGCCTGGCCTTGACTTGG T C TRMT61B Ensembl:ENSG00000171103 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1191806817 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_282561,RMVar_hsa_circ_271089,RMVar_hsa_circ_198127,RMVar_hsa_circ_198128,RMVar_hsa_circ_366187 31808 RMVar_ID_31808 Human_SNP_ID_65141201 A-to-I Human chr2 - 28855908 28855908 28855908 GGAGTGCAATGGCGTGATCTCGGCTCACTGCAATCTCTGCGTCCCTGGTTCAAGCATTTCTCCTG GGAGTGCAATGGCGTGATCTCGGCTCACTGCAGTCTCTGCGTCCCTGGTTCAAGCATTTCTCCTG T C TRMT61B Ensembl:ENSG00000171103 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1403753026 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_282561,RMVar_hsa_circ_271089,RMVar_hsa_circ_198127,RMVar_hsa_circ_198128,RMVar_hsa_circ_366187 31809 RMVar_ID_31809 Human_SNP_ID_65141414 A-to-I Human chr2 - 28856773 28856773 28856773 AAAATTAGTTGGGTGTGGTGGCGCATGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAAGAGA AAAATTAGTTGGGTGTGGTGGCGCATGCCTGTCATCCCAGCTACTCGGGAGGCTGAGGCAAGAGA T G TRMT61B Ensembl:ENSG00000171103 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs944807631 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_282561,RMVar_hsa_circ_271089,RMVar_hsa_circ_198127,RMVar_hsa_circ_198128,RMVar_hsa_circ_366187 31810 RMVar_ID_31810 Human_SNP_ID_65141911 A-to-I Human chr2 - 28858632 28858632 28858632 CGCCACCATGGCTGGCTAGTTTTTGTGTTTTTAGTAGAGATGGGGTTTCACCATGTTGCCTAGGC CGCCACCATGGCTGGCTAGTTTTTGTGTTTTTTGTAGAGATGGGGTTTCACCATGTTGCCTAGGC T A TRMT61B Ensembl:ENSG00000171103 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1173796404 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_282561,RMVar_hsa_circ_271089,RMVar_hsa_circ_198127,RMVar_hsa_circ_198128,RMVar_hsa_circ_366187 31811 RMVar_ID_31811 Human_SNP_ID_65142058 A-to-I Human chr2 - 28858992 28858992 28858992 TACTTGGGAGGCCGAGTCAGGAGAATCGCTTGAACCTGGGAGGCGGAGGTTCCAGTGAGCCAAGA TACTTGGGAGGCCGAGTCAGGAGAATCGCTTGGACCTGGGAGGCGGAGGTTCCAGTGAGCCAAGA T C TRMT61B Ensembl:ENSG00000171103 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1349888649 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25532189 RMVar_hsa_circ_282561,RMVar_hsa_circ_271089,RMVar_hsa_circ_198127,RMVar_hsa_circ_198128,RMVar_hsa_circ_366187 31812 RMVar_ID_31812 Human_SNP_ID_65143206 A-to-I Human chr2 - 28863173 28863173 28863173 CCTAAGCCTCCCAAAGTGCTGGGATTACAGGCATGGGGCACCACGCCCAGCTTATGTTACTATTA CCTAAGCCTCCCAAAGTGCTGGGATTACAGGCGTGGGGCACCACGCCCAGCTTATGTTACTATTA T C TRMT61B Ensembl:ENSG00000171103 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1013692243 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_282561,RMVar_hsa_circ_198128,RMVar_hsa_circ_322658,RMVar_hsa_circ_366187 31813 RMVar_ID_31813 Human_SNP_ID_65143237 A-to-I Human chr2 - 28863323 28863323 28863323 GAACTCAAGTGATCCTGTCGTCCCAGCCTCCCAAGTAGGTGGGACAATAGGCACATACCACCAAA GAACTCAAGTGATCCTGTCGTCCCAGCCTCCCGAGTAGGTGGGACAATAGGCACATACCACCAAA T C TRMT61B Ensembl:ENSG00000171103 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1430457771 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_282561,RMVar_hsa_circ_198128,RMVar_hsa_circ_322658,RMVar_hsa_circ_366187 31814 RMVar_ID_31814 Human_SNP_ID_65143253 A-to-I Human chr2 - 28863371 28863371 28863371 TTTGGAATGCAGTGGTATGATCGTGGCTCACTACAGCCTTGACCCTCGGAACTCAAGTGATCCTG TTTGGAATGCAGTGGTATGATCGTGGCTCACTGCAGCCTTGACCCTCGGAACTCAAGTGATCCTG T C TRMT61B Ensembl:ENSG00000171103 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1460805544 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13850572 RMVar_hsa_circ_282561,RMVar_hsa_circ_198128,RMVar_hsa_circ_322658,RMVar_hsa_circ_366187 31815 RMVar_ID_31815 Human_SNP_ID_65144294 A-to-I Human chr2 - 28867242 28867242 28867242 AAAAATAAAAAATTAGCCAGGTATGCTGGCACACACTTGTGGTCCCAGCTACGCAGGAGGCTGAG AAAAATAAAAAATTAGCCAGGTATGCTGGCACTCACTTGTGGTCCCAGCTACGCAGGAGGCTGAG T A TRMT61B Ensembl:ENSG00000171103 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1183339083 Functional Loss SNV dbSNP153 33..33 33 - - - 31816 RMVar_ID_31816 Human_SNP_ID_65144295 A-to-I Human chr2 - 28867256 28867256 28867256 ACCTTGTCTCTACAAAAAATAAAAAATTAGCCAGGTATGCTGGCACACACTTGTGGTCCCAGCTA ACCTTGTCTCTACAAAAAATAAAAAATTAGCCCGGTATGCTGGCACACACTTGTGGTCCCAGCTA T G TRMT61B Ensembl:ENSG00000171103 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1416844544 Functional Loss SNV dbSNP153 33..33 33 - - - 31817 RMVar_ID_31817 Human_SNP_ID_65144301 A-to-I Human chr2 - 28867294 28867294 28867294 GCCCAGAAGTTTGAGACCAGCCGGGGCAACATAGGGAGACCTTGTCTCTACAAAAAATAAAAAAT GCCCAGAAGTTTGAGACCAGCCGGGGCAACATTGGGAGACCTTGTCTCTACAAAAAATAAAAAAT T A TRMT61B Ensembl:ENSG00000171103 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1344558872 Functional Loss SNV dbSNP153 33..33 33 - - - 31818 RMVar_ID_31818 Human_SNP_ID_65144302 A-to-I Human chr2 - 28867294 28867294 28867294 GCCCAGAAGTTTGAGACCAGCCGGGGCAACATAGGGAGACCTTGTCTCTACAAAAAATAAAAAAT GCCCAGAAGTTTGAGACCAGCCGGGGCAACATGGGGAGACCTTGTCTCTACAAAAAATAAAAAAT T C TRMT61B Ensembl:ENSG00000171103 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1344558872 Functional Loss SNV dbSNP153 33..33 33 - - - 31819 RMVar_ID_31819 Human_SNP_ID_65144453 A-to-I Human chr2 - 28867968 28867968 28867968 CTCTTACTGTAGCCTGAACCTCCCAGGCTCCAACAATCCTCGCACCTCAACCTCCTGAGTAGCTG CTCTTACTGTAGCCTGAACCTCCCAGGCTCCAGCAATCCTCGCACCTCAACCTCCTGAGTAGCTG T C TRMT61B Ensembl:ENSG00000171103 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs750420032 Functional Loss SNV dbSNP153 33..33 33 - - - 31820 RMVar_ID_31820 Human_SNP_ID_65144464 A-to-I Human chr2 - 28868045 28868045 28868045 GAGGTATAATAAGCTTTTTTTGTTTAAAGACAAGGTCTTGCTATGTCACCCAGGCTAGAGTGCAG GAGGTATAATAAGCTTTTTTTGTTTAAAGACAGGGTCTTGCTATGTCACCCAGGCTAGAGTGCAG T C TRMT61B Ensembl:ENSG00000171103 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1156926845 Functional Loss SNV dbSNP153 33..33 33 - - - 31821 RMVar_ID_31821 Human_SNP_ID_65144646 A-to-I Human chr2 - 28868795 28868795 28868795 TTGCCCAGGCTGGTCTTCAACTCGTGGCCTCAAGTGATCCGCCCACCTCGGCCTCCCAGTGCTGG TTGCCCAGGCTGGTCTTCAACTCGTGGCCTCAGGTGATCCGCCCACCTCGGCCTCCCAGTGCTGG T C TRMT61B Ensembl:ENSG00000171103 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1423263829 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25532240 31822 RMVar_ID_31822 Human_SNP_ID_65155379 A-to-I Human chr2 + 28908248 28908248 28908248 AGAAGAGATACATGGTTTTGGGGTTTTTAGACAAGTTGGCTTTGAAATAACATTATGTGAAAGAT AGAAGAGATACATGGTTTTGGGGTTTTTAGACGAGTTGGCTTTGAAATAACATTATGTGAAAGAT A G WDR43 Ensembl:ENSG00000163811 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7584370 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13851360 GWAS_ID_3558,GWAS_ID_3559 RMVar_hsa_circ_99946,RMVar_hsa_circ_354345,RMVar_hsa_circ_356766,RMVar_hsa_circ_360567,RMVar_hsa_circ_341660,RMVar_hsa_circ_276733,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_198134,RMVar_hsa_circ_198132,RMVar_hsa_circ_288289,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_288307,RMVar_hsa_circ_269901,RMVar_hsa_circ_286168,RMVar_hsa_circ_111760,RMVar_hsa_circ_198137,RMVar_hsa_circ_198139,RMVar_hsa_circ_198140,RMVar_hsa_circ_198138,RMVar_hsa_circ_198136 31823 RMVar_ID_31823 Human_SNP_ID_65155697 A-to-I Human chr2 + 28909474 28909474 28909474 CTTCTTTTGTTCCTTACATCCTGTCTATTGTGAGTGTGTTTTGATTTGTTTGATTTGGCCTCTTT CTTCTTTTGTTCCTTACATCCTGTCTATTGTGGGTGTGTTTTGATTTGTTTGATTTGGCCTCTTT A G WDR43 Ensembl:ENSG00000163811 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs13426929 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2636413,Human_RBP_ID_3622573,Human_RBP_ID_6908571,Human_RBP_ID_23866535 RMVar_hsa_circ_99946,RMVar_hsa_circ_354345,RMVar_hsa_circ_356766,RMVar_hsa_circ_360567,RMVar_hsa_circ_341660,RMVar_hsa_circ_276733,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_198134,RMVar_hsa_circ_198132,RMVar_hsa_circ_288289,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_288307,RMVar_hsa_circ_269901,RMVar_hsa_circ_286168,RMVar_hsa_circ_111760,RMVar_hsa_circ_198137,RMVar_hsa_circ_198139,RMVar_hsa_circ_198140,RMVar_hsa_circ_198138,RMVar_hsa_circ_198136 31824 RMVar_ID_31824 Human_SNP_ID_65155698 A-to-I Human chr2 + 28909474 28909474 28909474 CTTCTTTTGTTCCTTACATCCTGTCTATTGTGAGTGTGTTTTGATTTGTTTGATTTGGCCTCTTT CTTCTTTTGTTCCTTACATCCTGTCTATTGTGTGTGTGTTTTGATTTGTTTGATTTGGCCTCTTT A T WDR43 Ensembl:ENSG00000163811 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs13426929 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2636413,Human_RBP_ID_3622573,Human_RBP_ID_6908571,Human_RBP_ID_23866535 RMVar_hsa_circ_99946,RMVar_hsa_circ_354345,RMVar_hsa_circ_356766,RMVar_hsa_circ_360567,RMVar_hsa_circ_341660,RMVar_hsa_circ_276733,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_198134,RMVar_hsa_circ_198132,RMVar_hsa_circ_288289,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_288307,RMVar_hsa_circ_269901,RMVar_hsa_circ_286168,RMVar_hsa_circ_111760,RMVar_hsa_circ_198137,RMVar_hsa_circ_198139,RMVar_hsa_circ_198140,RMVar_hsa_circ_198138,RMVar_hsa_circ_198136 31825 RMVar_ID_31825 Human_SNP_ID_65155762 A-to-I Human chr2 + 28909709 28909709 28909709 GTCCTGGGAAACATAGTGAGAACCCCCTCTCTACAAAAATGAAAAAAATTAGCCAGATGTGGTGG GTCCTGGGAAACATAGTGAGAACCCCCTCTCTCCAAAAATGAAAAAAATTAGCCAGATGTGGTGG A C WDR43 Ensembl:ENSG00000163811 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs950236521 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25532397 RMVar_hsa_circ_99946,RMVar_hsa_circ_354345,RMVar_hsa_circ_356766,RMVar_hsa_circ_360567,RMVar_hsa_circ_341660,RMVar_hsa_circ_276733,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_198134,RMVar_hsa_circ_198132,RMVar_hsa_circ_288289,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_288307,RMVar_hsa_circ_269901,RMVar_hsa_circ_286168,RMVar_hsa_circ_111760,RMVar_hsa_circ_198137,RMVar_hsa_circ_198139,RMVar_hsa_circ_198140,RMVar_hsa_circ_198138,RMVar_hsa_circ_198136 31826 RMVar_ID_31826 Human_SNP_ID_65155770 A-to-I Human chr2 + 28909733 28909733 28909733 CCCTCTCTACAAAAATGAAAAAAATTAGCCAGATGTGGTGGTGTGTACCTGTAGTCCCAGCCACC CCCTCTCTACAAAAATGAAAAAAATTAGCCAGGTGTGGTGGTGTGTACCTGTAGTCCCAGCCACC A G WDR43 Ensembl:ENSG00000163811 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6739354 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_3560,GWAS_ID_3561,GWAS_ID_3562,GWAS_ID_3563,GWAS_ID_3564,GWAS_ID_3565,GWAS_ID_3566,GWAS_ID_3567,GWAS_ID_3568,GWAS_ID_3569,GWAS_ID_3570,GWAS_ID_3571,GWAS_ID_3572,GWAS_ID_3573,GWAS_ID_3574,GWAS_ID_3575,GWAS_ID_3576,GWAS_ID_3577,GWAS_ID_3578,GWAS_ID_3579,GWAS_ID_3580,GWAS_ID_3581,GWAS_ID_3582 RMVar_hsa_circ_99946,RMVar_hsa_circ_354345,RMVar_hsa_circ_356766,RMVar_hsa_circ_360567,RMVar_hsa_circ_341660,RMVar_hsa_circ_276733,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_198134,RMVar_hsa_circ_198132,RMVar_hsa_circ_288289,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_288307,RMVar_hsa_circ_269901,RMVar_hsa_circ_286168,RMVar_hsa_circ_111760,RMVar_hsa_circ_198137,RMVar_hsa_circ_198139,RMVar_hsa_circ_198140,RMVar_hsa_circ_198138,RMVar_hsa_circ_198136 31827 RMVar_ID_31827 Human_SNP_ID_65156130 A-to-I Human chr2 + 28910801 28910801 28910801 CTCACTGTAAACTCTGCCTCCGGGGTTCAAGCAATCCTCCTGTCTCAGCCTCCCGAGTACCTGGG CTCACTGTAAACTCTGCCTCCGGGGTTCAAGCGATCCTCCTGTCTCAGCCTCCCGAGTACCTGGG A G WDR43 Ensembl:ENSG00000163811 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1030469820 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13851433 RMVar_hsa_circ_99946,RMVar_hsa_circ_354345,RMVar_hsa_circ_356766,RMVar_hsa_circ_360567,RMVar_hsa_circ_341660,RMVar_hsa_circ_276733,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_198134,RMVar_hsa_circ_198132,RMVar_hsa_circ_288289,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_288307,RMVar_hsa_circ_269901,RMVar_hsa_circ_286168,RMVar_hsa_circ_111760,RMVar_hsa_circ_198137,RMVar_hsa_circ_198139,RMVar_hsa_circ_198140,RMVar_hsa_circ_198138,RMVar_hsa_circ_198136 31828 RMVar_ID_31828 Human_SNP_ID_65156520 A-to-I Human chr2 + 28912259 28912259 28912259 CTAGCCAGTATGGAACTTTCCTGGACATTCGCAAAGTTCATCTCCTGGGTCACAGGATGTACAAC CTAGCCAGTATGGAACTTTCCTGGACATTCGCGAAGTTCATCTCCTGGGTCACAGGATGTACAAC A G WDR43 Ensembl:ENSG00000163811 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6729601 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99946,RMVar_hsa_circ_354345,RMVar_hsa_circ_356766,RMVar_hsa_circ_360567,RMVar_hsa_circ_341660,RMVar_hsa_circ_276733,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_198134,RMVar_hsa_circ_198132,RMVar_hsa_circ_288289,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_288307,RMVar_hsa_circ_269901,RMVar_hsa_circ_286168,RMVar_hsa_circ_111760,RMVar_hsa_circ_198137,RMVar_hsa_circ_198139,RMVar_hsa_circ_198140,RMVar_hsa_circ_198138,RMVar_hsa_circ_198136 31829 RMVar_ID_31829 Human_SNP_ID_65158264 A-to-I Human chr2 + 28918424 28918424 28918424 GAGTTTCGCTCTTGTTGCCCAGGCTGGAGTGCAATGGCACGGTCGCGACTAACCACGACCTCTGC GAGTTTCGCTCTTGTTGCCCAGGCTGGAGTGCGATGGCACGGTCGCGACTAACCACGACCTCTGC A G WDR43 Ensembl:ENSG00000163811 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs191647131 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6908661,Human_RBP_ID_13851753,Human_RBP_ID_23866570 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_81358,RMVar_hsa_circ_198152,RMVar_hsa_circ_198154,RMVar_hsa_circ_198155,RMVar_hsa_circ_198153 31830 RMVar_ID_31830 Human_SNP_ID_65158966 A-to-I Human chr2 + 28920756 28920756 28920756 TGGAGTGCAGTGGTGTGATCTCAGCTCACTGCAAACTCTGCCTCCCAGGTTCGAGCATTTCTTCT TGGAGTGCAGTGGTGTGATCTCAGCTCACTGCGAACTCTGCCTCCCAGGTTCGAGCATTTCTTCT A G WDR43 Ensembl:ENSG00000163811 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs960093730 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13851862 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_81358,RMVar_hsa_circ_198152,RMVar_hsa_circ_198154,RMVar_hsa_circ_198155,RMVar_hsa_circ_198153 31831 RMVar_ID_31831 Human_SNP_ID_65194070 A-to-I Human chr2 + 29050273 29050273 29050273 CCAGCTACTGGGGAGGCTGAGGCAGGAGAATTACTTGAGCCTAGGAGGTCGAGACTGCAGTGAAC CCAGCTACTGGGGAGGCTGAGGCAGGAGAATTGCTTGAGCCTAGGAGGTCGAGACTGCAGTGAAC A G TOGARAM2 Ensembl:ENSG00000189350 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1248204136 Functional Loss SNV dbSNP153 33..33 33 - - - 31832 RMVar_ID_31832 Human_SNP_ID_65221100 A-to-I Human chr2 + 29149010 29149010 29149010 ATATTCTCTCAGTATATTTAAGGAGATACTCTATTGTCTCAGGTAGAGTTTGACAGACTTTTTCT ATATTCTCTCAGTATATTTAAGGAGATACTCTGTTGTCTCAGGTAGAGTTTGACAGACTTTTTCT A G CLIP4 Ensembl:ENSG00000115295 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167520048 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20261,RMVar_hsa_circ_353219,RMVar_hsa_circ_198169,RMVar_hsa_circ_366240,RMVar_hsa_circ_353764,RMVar_hsa_circ_46396,RMVar_hsa_circ_198172,RMVar_hsa_circ_315822,RMVar_hsa_circ_24745,RMVar_hsa_circ_198180,RMVar_hsa_circ_198174,RMVar_hsa_circ_10664,RMVar_hsa_circ_198173,RMVar_hsa_circ_62635,RMVar_hsa_circ_65732,RMVar_hsa_circ_302594,RMVar_hsa_circ_318816,RMVar_hsa_circ_327889,RMVar_hsa_circ_297747,RMVar_hsa_circ_280395,RMVar_hsa_circ_266596,RMVar_hsa_circ_4085,RMVar_hsa_circ_198182,RMVar_hsa_circ_198183,RMVar_hsa_circ_198184,RMVar_hsa_circ_198181,RMVar_hsa_circ_2557,RMVar_hsa_circ_39422 31833 RMVar_ID_31833 Human_SNP_ID_65229275 A-to-I Human chr2 + 29178940 29178940 29178940 CCTCAGCCTCTCGAGTAGCTGGGATTACAGGCACCTGCCACTGTGCCCTTCTAAGTTTTGTATTT CCTCAGCCTCTCGAGTAGCTGGGATTACAGGCCCCTGCCACTGTGCCCTTCTAAGTTTTGTATTT A C CLIP4 Ensembl:ENSG00000115295 Protein coding intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1000759547 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_198172,RMVar_hsa_circ_24745,RMVar_hsa_circ_327889,RMVar_hsa_circ_266596,RMVar_hsa_circ_198184,RMVar_hsa_circ_39422,RMVar_hsa_circ_284548,RMVar_hsa_circ_97932,RMVar_hsa_circ_198186,RMVar_hsa_circ_198185,RMVar_hsa_circ_344892,RMVar_hsa_circ_354254 31834 RMVar_ID_31834 Human_SNP_ID_65384573 A-to-I Human chr2 - 29786867 29786867 29786867 CGCTTGAACCTAGGAGGTAGGTAGAGGTTGCAATGAGTCAAGATTGTGCTGTTGCACTCCAGCCT CGCTTGAACCTAGGAGGTAGGTAGAGGTTGCAGTGAGTCAAGATTGTGCTGTTGCACTCCAGCCT T C ALK Ensembl:ENSG00000171094 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1194567847 Functional Loss SNV dbSNP153 33..33 33 - - - 31835 RMVar_ID_31835 Human_SNP_ID_481490743 A-to-I Human chr11 - 110050005 110050005 110050005 CAGCTGGTTCTCTCGGAGCTTATATAGGGCCAACAGCACTGTCACCTCCTCCTTGGTCATGACAA CAGCTGGTTCTCTCGGAGCTTATATAGGGCCAGCAGCACTGTCACCTCCTCCTTGGTCATGACAA T C RDX Ensembl:ENSG00000137710 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs994203649 Functional Loss SNV dbSNP153 33..33 33 - - - 31836 RMVar_ID_31836 Human_SNP_ID_481490778 A-to-I Human chr11 + 110050087 110050087 110050087 GGACGCCGTGGCGCGCTACTTTGGGATAAAGCATGGGCAGGTAGTGAAGATCATCCGGCCCAGCG GGACGCCGTGGCGCGCTACTTTGGGATAAAGCGTGGGCAGGTAGTGAAGATCATCCGGCCCAGCG A G AP001889.1 Ensembl:ENSG00000255210 Pseudogene exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1421679212 Functional Loss SNV dbSNP153 33..33 33 - - - 31837 RMVar_ID_31837 Human_SNP_ID_481516769 A-to-I Human chr11 + 110159750 110159750 110159750 AACACCTAAGGTAGAGGAAGTCTTCTAAGACTATGTCTGGAGAACCTGAGGAAACAGACACTGGG AACACCTAAGGTAGAGGAAGTCTTCTAAGACTGTGTCTGGAGAACCTGAGGAAACAGACACTGGG A G ZC3H12C Ensembl:ENSG00000149289 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs623236 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_153029,RMVar_hsa_circ_274978 31838 RMVar_ID_31838 Human_SNP_ID_481538520 A-to-I Human chr11 - 110244240 110244240 110244240 CTTCTGTCTCAGCCTCCTGAGTAGCTGGGATTACAGGCGTCCACCACCACACCCAGCTAATTTTT CTTCTGTCTCAGCCTCCTGAGTAGCTGGGATTCCAGGCGTCCACCACCACACCCAGCTAATTTTT T G RDX Ensembl:ENSG00000137710 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1414338358 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_358943,RMVar_hsa_circ_364496,RMVar_hsa_circ_333102,RMVar_hsa_circ_362100,RMVar_hsa_circ_352645 31839 RMVar_ID_31839 Human_SNP_ID_481539164 A-to-I Human chr11 - 110246627 110246627 110246627 GGGATTACAGGCGTACTCCACCAGGCCCAGCTAATTTTTGTATTTTTAGTAGAGAGAGGGTTTCG GGGATTACAGGCGTACTCCACCAGGCCCAGCTGATTTTTGTATTTTTAGTAGAGAGAGGGTTTCG T C RDX Ensembl:ENSG00000137710 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1426948263 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_358943,RMVar_hsa_circ_364496,RMVar_hsa_circ_333102,RMVar_hsa_circ_362100,RMVar_hsa_circ_352645 31840 RMVar_ID_31840 Human_SNP_ID_481543309 A-to-I Human chr11 - 110263273 110263273 110263273 TAGAATTCTCTGACTTTTTCCCCCCCCGAGATAGAGCCTCACTCTGTCACCCAGGCTGGAGTGCA TAGAATTCTCTGACTTTTTCCCCCCCCGAGATGGAGCCTCACTCTGTCACCCAGGCTGGAGTGCA T C RDX Ensembl:ENSG00000137710 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs530820717 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_751049,Human_RBP_ID_11520810 RMVar_hsa_circ_358943,RMVar_hsa_circ_356221,RMVar_hsa_circ_342248,RMVar_hsa_circ_71375,RMVar_hsa_circ_355979,RMVar_hsa_circ_57247,RMVar_hsa_circ_67209,RMVar_hsa_circ_366880 31841 RMVar_ID_31841 Human_SNP_ID_481543310 A-to-I Human chr11 - 110263273 110263273 110263273 TAGAATTCTCTGACTTTTTCCCCCCCCGAGATAGAGCCTCACTCTGTCACCCAGGCTGGAGTGCA TAGAATTCTCTGACTTTTTCCCCCCCCGAGATCGAGCCTCACTCTGTCACCCAGGCTGGAGTGCA T G RDX Ensembl:ENSG00000137710 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs530820717 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_751049,Human_RBP_ID_11520810 RMVar_hsa_circ_358943,RMVar_hsa_circ_356221,RMVar_hsa_circ_342248,RMVar_hsa_circ_71375,RMVar_hsa_circ_355979,RMVar_hsa_circ_57247,RMVar_hsa_circ_67209,RMVar_hsa_circ_366880 31842 RMVar_ID_31842 Human_SNP_ID_481543967 A-to-I Human chr11 - 110265229 110265229 110265229 AAAATTAGCTAGGCGTGGTAGTGCATACCTGTAATCACAGCTACTTTGGAGGCTGAGGCAGGAGA AAAATTAGCTAGGCGTGGTAGTGCATACCTGTGATCACAGCTACTTTGGAGGCTGAGGCAGGAGA T C RDX Ensembl:ENSG00000137710 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1352056986 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_358943,RMVar_hsa_circ_356221,RMVar_hsa_circ_355979,RMVar_hsa_circ_57247,RMVar_hsa_circ_366880,RMVar_hsa_circ_317062,RMVar_hsa_circ_332060 31843 RMVar_ID_31843 Human_SNP_ID_481543982 A-to-I Human chr11 - 110265295 110265295 110265295 CTGAGGTCAGGAGTTTGAGACCAACCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACA CTGAGGTCAGGAGTTTGAGACCAACCTGGCCACCATGGTGAAACCCCATCTCTACTAAAAATACA T G RDX Ensembl:ENSG00000137710 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1565323534 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_358943,RMVar_hsa_circ_356221,RMVar_hsa_circ_355979,RMVar_hsa_circ_57247,RMVar_hsa_circ_366880,RMVar_hsa_circ_317062,RMVar_hsa_circ_332060 31844 RMVar_ID_31844 Human_SNP_ID_481544004 A-to-I Human chr11 - 110265367 110265367 110265367 GGATTAGAGGCCAGGTGCAGTGGCTTACGCCTATAATCCCAAGACTTTGGAAGGCCGAGGCAGGC GGATTAGAGGCCAGGTGCAGTGGCTTACGCCTGTAATCCCAAGACTTTGGAAGGCCGAGGCAGGC T C RDX Ensembl:ENSG00000137710 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs901919267 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_358943,RMVar_hsa_circ_356221,RMVar_hsa_circ_355979,RMVar_hsa_circ_57247,RMVar_hsa_circ_366880,RMVar_hsa_circ_317062,RMVar_hsa_circ_332060 31845 RMVar_ID_31845 Human_SNP_ID_481544213 A-to-I Human chr11 - 110266135 110266135 110266135 TATTTTTAGTAGTGATGAAGTTTCACCGTGTTAGTCAGGATGGTCTTGATCTCCTGACTTTGTGA TATTTTTAGTAGTGATGAAGTTTCACCGTGTTGGTCAGGATGGTCTTGATCTCCTGACTTTGTGA T C RDX Ensembl:ENSG00000137710 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1297583286 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_358943,RMVar_hsa_circ_356221,RMVar_hsa_circ_355979,RMVar_hsa_circ_57247,RMVar_hsa_circ_366880,RMVar_hsa_circ_317062,RMVar_hsa_circ_332060 31846 RMVar_ID_31846 Human_SNP_ID_481544409 A-to-I Human chr11 - 110266728 110266728 110266728 AAAACAAAACAAAACAAAAAAAAACATTAACTAGGTGTGGTGGAATGTGCCTCTAGTCCCAGCCA AAAACAAAACAAAACAAAAAAAAACATTAACTGGGTGTGGTGGAATGTGCCTCTAGTCCCAGCCA T C RDX Ensembl:ENSG00000137710 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1459498001 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_358943,RMVar_hsa_circ_356221,RMVar_hsa_circ_355979,RMVar_hsa_circ_57247,RMVar_hsa_circ_366880,RMVar_hsa_circ_317062,RMVar_hsa_circ_332060 31847 RMVar_ID_31847 Human_SNP_ID_481544536 A-to-I Human chr11 - 110267067 110267067 110267067 AGACCCTATCTCTACTAAAAATATAAAAAATTAGCTAGGTTTGGTGGTGCATGCCTGTGGTCCGA AGACCCTATCTCTACTAAAAATATAAAAAATTGGCTAGGTTTGGTGGTGCATGCCTGTGGTCCGA T C RDX Ensembl:ENSG00000137710 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1439249471 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_358943,RMVar_hsa_circ_356221,RMVar_hsa_circ_355979,RMVar_hsa_circ_57247,RMVar_hsa_circ_366880,RMVar_hsa_circ_317062,RMVar_hsa_circ_332060 31848 RMVar_ID_31848 Human_SNP_ID_481544537 A-to-I Human chr11 - 110267067 110267067 110267067 AGACCCTATCTCTACTAAAAATATAAAAAATTAGCTAGGTTTGGTGGTGCATGCCTGTGGTCCGA AGACCCTATCTCTACTAAAAATATAAAAAATTCGCTAGGTTTGGTGGTGCATGCCTGTGGTCCGA T G RDX Ensembl:ENSG00000137710 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1439249471 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_358943,RMVar_hsa_circ_356221,RMVar_hsa_circ_355979,RMVar_hsa_circ_57247,RMVar_hsa_circ_366880,RMVar_hsa_circ_317062,RMVar_hsa_circ_332060 31849 RMVar_ID_31849 Human_SNP_ID_481544542 A-to-I Human chr11 - 110267086 110267086 110267086 CAGCCTGGGCAACATAGTGAGACCCTATCTCTACTAAAAATATAAAAAATTAGCTAGGTTTGGTG CAGCCTGGGCAACATAGTGAGACCCTATCTCTTCTAAAAATATAAAAAATTAGCTAGGTTTGGTG T A RDX Ensembl:ENSG00000137710 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1056505605 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_358943,RMVar_hsa_circ_356221,RMVar_hsa_circ_355979,RMVar_hsa_circ_57247,RMVar_hsa_circ_366880,RMVar_hsa_circ_317062,RMVar_hsa_circ_332060 31850 RMVar_ID_31850 Human_SNP_ID_481544613 A-to-I Human chr11 - 110267365 110267365 110267365 GGGATTATGGGTGTGCACCACCACACCTGGCTAATTTTTGTATTTTTAGCAGAGATGGGGTTTCA GGGATTATGGGTGTGCACCACCACACCTGGCTGATTTTTGTATTTTTAGCAGAGATGGGGTTTCA T C RDX Ensembl:ENSG00000137710 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1044135841 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_358943,RMVar_hsa_circ_356221,RMVar_hsa_circ_355979,RMVar_hsa_circ_57247,RMVar_hsa_circ_366880,RMVar_hsa_circ_317062,RMVar_hsa_circ_332060 31851 RMVar_ID_31851 Human_SNP_ID_481545169 A-to-I Human chr11 - 110269118 110269118 110269118 GCAAAACTGTCTCTACTAAAAATGCAAACATTAGCTGAGTGTGGTGGTGCACACTTGTAATCCCA GCAAAACTGTCTCTACTAAAAATGCAAACATTGGCTGAGTGTGGTGGTGCACACTTGTAATCCCA T C RDX Ensembl:ENSG00000137710 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs944343018 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_358943,RMVar_hsa_circ_356221,RMVar_hsa_circ_355979,RMVar_hsa_circ_57247,RMVar_hsa_circ_366880,RMVar_hsa_circ_317062,RMVar_hsa_circ_332060 31852 RMVar_ID_31852 Human_SNP_ID_481545349 A-to-I Human chr11 - 110269820 110269820 110269820 TTTCCCAGGCTGGTCTTGAACTTCTGAGCTCAAGTGATCCGCCTCCCTCGGCCTCCCAAAGTGCC TTTCCCAGGCTGGTCTTGAACTTCTGAGCTCAGGTGATCCGCCTCCCTCGGCCTCCCAAAGTGCC T C RDX Ensembl:ENSG00000137710 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1208257517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24867508 RMVar_hsa_circ_358943,RMVar_hsa_circ_356221,RMVar_hsa_circ_355979,RMVar_hsa_circ_57247,RMVar_hsa_circ_366880,RMVar_hsa_circ_317062,RMVar_hsa_circ_332060 31853 RMVar_ID_31853 Human_SNP_ID_481545379 A-to-I Human chr11 - 110269920 110269920 110269920 CTCCCACCTCAGCCTCTTGAGTAGCTGGGACCACAAGTGTGCTCCACCATGCCCGGCTAATTTTT CTCCCACCTCAGCCTCTTGAGTAGCTGGGACCGCAAGTGTGCTCCACCATGCCCGGCTAATTTTT T C RDX Ensembl:ENSG00000137710 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1181138750 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_358943,RMVar_hsa_circ_356221,RMVar_hsa_circ_355979,RMVar_hsa_circ_57247,RMVar_hsa_circ_366880,RMVar_hsa_circ_317062,RMVar_hsa_circ_332060 31854 RMVar_ID_31854 Human_SNP_ID_481547864 A-to-I Human chr11 - 110279443 110279443 110279443 CGGCTCACTGCAACCTCTCCTTTCTGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCTGAGTAGCT CGGCTCACTGCAACCTCTCCTTTCTGGGTTCAGGTGATTCTCCTGCCTCAGCCTCCTGAGTAGCT T C RDX Ensembl:ENSG00000137710 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985316337 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_358943,RMVar_hsa_circ_356221,RMVar_hsa_circ_355979,RMVar_hsa_circ_153033,RMVar_hsa_circ_317062,RMVar_hsa_circ_319003 31855 RMVar_ID_31855 Human_SNP_ID_481548736 A-to-I Human chr11 - 110282722 110282722 110282722 CTCCTGCGTTGGCCTCCCAAAGTGCTGGAATTACAGGTGTGAGCCACCATGCCTGGCTACTATGG CTCCTGCGTTGGCCTCCCAAAGTGCTGGAATTTCAGGTGTGAGCCACCATGCCTGGCTACTATGG T A RDX Ensembl:ENSG00000137710 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs140931918 Functional Loss SNV dbSNP153 33..33 33 - - - 31856 RMVar_ID_31856 Human_SNP_ID_481549456 A-to-I Human chr11 - 110285298 110285298 110285298 TCACTGCAGCCCCTGCCTCCCAGGTTCGTGCAATTCTGCTATCTCAGCCTCCCCAGTAGCTGAGA TCACTGCAGCCCCTGCCTCCCAGGTTCGTGCAGTTCTGCTATCTCAGCCTCCCCAGTAGCTGAGA T C RDX Ensembl:ENSG00000137710 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1294543773 Functional Loss SNV dbSNP153 33..33 33 - - - 31857 RMVar_ID_31857 Human_SNP_ID_481567941 A-to-I Human chr11 + 110355792 110355788 110355792 CCCTTTATTTATTTATTTAGAGACAGAGTCTCACTCTGTCACCCAGGCTAGAGTGCACACCTCAC CCCTTTATTTATTTATTTAGAGACAGAGT____CTCTGTCACCCAGGCTAGAGTGCACACCTCAC TCTCA T LINC02732 Ensembl:ENSG00000254416 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs972796666 Functional Loss DEL dbSNP153 30..33 33 - - - 31858 RMVar_ID_31858 Human_SNP_ID_481567942 A-to-I Human chr11 + 110355792 110355792 110355792 CCCTTTATTTATTTATTTAGAGACAGAGTCTCACTCTGTCACCCAGGCTAGAGTGCACACCTCAC CCCTTTATTTATTTATTTAGAGACAGAGTCTCCCTCTGTCACCCAGGCTAGAGTGCACACCTCAC A C LINC02732 Ensembl:ENSG00000254416 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1393708748 Functional Loss SNV dbSNP153 33..33 33 - - - 31859 RMVar_ID_31859 Human_SNP_ID_481567943 A-to-I Human chr11 + 110355792 110355792 110355792 CCCTTTATTTATTTATTTAGAGACAGAGTCTCACTCTGTCACCCAGGCTAGAGTGCACACCTCAC CCCTTTATTTATTTATTTAGAGACAGAGTCTCGCTCTGTCACCCAGGCTAGAGTGCACACCTCAC A G LINC02732 Ensembl:ENSG00000254416 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1393708748 Functional Loss SNV dbSNP153 33..33 33 - - - 31860 RMVar_ID_31860 Human_SNP_ID_481572601 A-to-I Human chr11 + 110374261 110374261 110374261 GCTGGGATTACAAAACAGAATTGCTTGAACCCAGGAGGGAGAGGTTGCAGTGAGCTGAGATGGCG GCTGGGATTACAAAACAGAATTGCTTGAACCCGGGAGGGAGAGGTTGCAGTGAGCTGAGATGGCG A G LINC02732 Ensembl:ENSG00000254416 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs540366312 Functional Loss SNV dbSNP153 33..33 33 - - - 31861 RMVar_ID_31861 Human_SNP_ID_481871079 A-to-I Human chr11 + 111622461 111622461 111622461 GTATTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGGTCTCGATCACCTGACATCGTGA GTATTTTAGTAGAGACGGGGTTTCACCGTGTTTGCCAGGATGGTCTCGATCACCTGACATCGTGA A T SIK2 Ensembl:ENSG00000170145 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs997996730 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_153045,RMVar_hsa_circ_369876 31862 RMVar_ID_31862 Human_SNP_ID_481878890 A-to-I Human chr11 + 111658600 111658600 111658600 CTCCATCTCTACAAAAAACACAAAAATTAGCCAGGCACAGTGGCATATGCCTGTAGTCCTAGCTA CTCCATCTCTACAAAAAACACAAAAATTAGCCGGGCACAGTGGCATATGCCTGTAGTCCTAGCTA A G SIK2 Ensembl:ENSG00000170145 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs570011741 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_153045,RMVar_hsa_circ_369876 31863 RMVar_ID_31863 Human_SNP_ID_481891198 A-to-I Human chr11 - 111715984 111715984 111715984 CAGCCTGGCCAACATGGCAAAACCCCATCTCTACTAAAAGTACAGAACTTAGCTGGGTGTGGTGG CAGCCTGGCCAACATGGCAAAACCCCATCTCTGCTAAAAGTACAGAACTTAGCTGGGTGTGGTGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1240756433 Functional Loss SNV dbSNP153 33..33 33 - - - 31864 RMVar_ID_31864 Human_SNP_ID_481891444 A-to-I Human chr11 - 111717133 111717133 111717133 TTTTCTTGCATTTTTAGTAGAGATGGGGTTTCACCATGTTAGCCAGGATGGTCTCGATCTCCTGA TTTTCTTGCATTTTTAGTAGAGATGGGGTTTCCCCATGTTAGCCAGGATGGTCTCGATCTCCTGA T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968151371 Functional Loss SNV dbSNP153 33..33 33 - - - 31865 RMVar_ID_31865 Human_SNP_ID_481894568 A-to-I Human chr11 - 111728556 111728556 111728556 GGTCGGGTGTGGTGGCTCACACCTGTAATCCCAGTACTTTGGGAGGCCAAGGTGGGTGGGTCACC GGTCGGGTGTGGTGGCTCACACCTGTAATCCCGGTACTTTGGGAGGCCAAGGTGGGTGGGTCACC T C PPP2R1B Ensembl:ENSG00000137713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982338130 Functional Loss SNV dbSNP153 33..33 33 - - - 31866 RMVar_ID_31866 Human_SNP_ID_481894585 A-to-I Human chr11 + 111728610 111728610 111728610 CACACCCGACCTGGAATTTTTTTATAGAACTTATCTTCAGAGCAATGTATGAAAGACAAGAGCAG CACACCCGACCTGGAATTTTTTTATAGAACTTGTCTTCAGAGCAATGTATGAAAGACAAGAGCAG A G SIK2 Ensembl:ENSG00000170145 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs113423503 Functional Loss SNV dbSNP153 33..33 33 - - - 31867 RMVar_ID_31867 Human_SNP_ID_481894586 A-to-I Human chr11 + 111728610 111728610 111728610 CACACCCGACCTGGAATTTTTTTATAGAACTTATCTTCAGAGCAATGTATGAAAGACAAGAGCAG CACACCCGACCTGGAATTTTTTTATAGAACTTTTCTTCAGAGCAATGTATGAAAGACAAGAGCAG A T SIK2 Ensembl:ENSG00000170145 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs113423503 Functional Loss SNV dbSNP153 33..33 33 - - - 31868 RMVar_ID_31868 Human_SNP_ID_481894625 A-to-I Human chr11 + 111728700 111728700 111728700 CCTGTAATCCCAACACTTTGGGAGGCCAAGGCAGGCGGATCACGAGGTCAGGAGATTGAGACCAT CCTGTAATCCCAACACTTTGGGAGGCCAAGGCGGGCGGATCACGAGGTCAGGAGATTGAGACCAT A G SIK2 Ensembl:ENSG00000170145 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1219093351 Functional Loss SNV dbSNP153 33..33 33 - - - 31869 RMVar_ID_31869 Human_SNP_ID_481894643 A-to-I Human chr11 + 111728741 111728741 111728741 ACGAGGTCAGGAGATTGAGACCATCCTAACACAGTGAAACGCCGTCTCTACTAAAAATACAAAAA ACGAGGTCAGGAGATTGAGACCATCCTAACACGGTGAAACGCCGTCTCTACTAAAAATACAAAAA A G SIK2 Ensembl:ENSG00000170145 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs918543485 Functional Loss SNV dbSNP153 33..33 33 - - - 31870 RMVar_ID_31870 Human_SNP_ID_481894732 A-to-I Human chr11 + 111728873 111728873 111728873 GTGAACCCGGGAGGTGGAGCTTGCAGTGAGCCAAGATCGTGCCACTGCACTCCAGCCTGGGCGAC GTGAACCCGGGAGGTGGAGCTTGCAGTGAGCCCAGATCGTGCCACTGCACTCCAGCCTGGGCGAC A C SIK2 Ensembl:ENSG00000170145 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs57734892 Functional Loss SNV dbSNP153 33..33 33 - - - 31871 RMVar_ID_31871 Human_SNP_ID_481894733 A-to-I Human chr11 + 111728873 111728873 111728873 GTGAACCCGGGAGGTGGAGCTTGCAGTGAGCCAAGATCGTGCCACTGCACTCCAGCCTGGGCGAC GTGAACCCGGGAGGTGGAGCTTGCAGTGAGCCGAGATCGTGCCACTGCACTCCAGCCTGGGCGAC A G SIK2 Ensembl:ENSG00000170145 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs57734892 Functional Loss SNV dbSNP153 33..33 33 - - - 31872 RMVar_ID_31872 Human_SNP_ID_481895260 A-to-I Human chr11 + 111730564 111730564 111730564 TTTGGTCTGAAAGAGTTACTTTTGATAAAGTTAATCTAACTGTAGTTATATTTTCTGTGTGCTTT TTTGGTCTGAAAGAGTTACTTTTGATAAAGTTGATCTAACTGTAGTTATATTTTCTGTGTGCTTT A G SIK2 Ensembl:ENSG00000170145 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1378526021 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3368100 Human_miRNA_ID_150159,Human_miRNA_ID_1209870 31873 RMVar_ID_31873 Human_SNP_ID_481897709 A-to-I Human chr11 - 111740446 111740446 111740446 AAAAAGCACCTATTTGGGATCATTTGAGGTCAAGAATTCGAGATCAGCCTGACCAACATGGTGAA AAAAAGCACCTATTTGGGATCATTTGAGGTCAGGAATTCGAGATCAGCCTGACCAACATGGTGAA T C PPP2R1B Ensembl:ENSG00000137713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs374471199 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11522510 Human_miRNA_ID_1688713 RMVar_hsa_circ_59926 31874 RMVar_ID_31874 Human_SNP_ID_481900333 A-to-I Human chr11 - 111751812 111751812 111751812 CCACCACACCCAGCTAATTTTGTATTTTTAATAGAGATGGGGTTTTACCATGTTGGTCAGGCTGG CCACCACACCCAGCTAATTTTGTATTTTTAATGGAGATGGGGTTTTACCATGTTGGTCAGGCTGG T C PPP2R1B Ensembl:ENSG00000137713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1217372675 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41061,RMVar_hsa_circ_61779,RMVar_hsa_circ_59926,RMVar_hsa_circ_66544,RMVar_hsa_circ_367893,RMVar_hsa_circ_319038,RMVar_hsa_circ_333796,RMVar_hsa_circ_60907,RMVar_hsa_circ_61542,RMVar_hsa_circ_59706,RMVar_hsa_circ_153048,RMVar_hsa_circ_98866,RMVar_hsa_circ_289438,RMVar_hsa_circ_357109,RMVar_hsa_circ_279169,RMVar_hsa_circ_153050,RMVar_hsa_circ_153051,RMVar_hsa_circ_153049,RMVar_hsa_circ_153052,RMVar_hsa_circ_35888,RMVar_hsa_circ_331956,RMVar_hsa_circ_350067,RMVar_hsa_circ_56575,RMVar_hsa_circ_153053 31875 RMVar_ID_31875 Human_SNP_ID_481902579 A-to-I Human chr11 - 111760534 111760534 111760534 AGTGATCCTCCAGCCTCAGCCTCCAAGTAGCTAGGACTACCGACATACACTACTGCGCCTGGCTA AGTGATCCTCCAGCCTCAGCCTCCAAGTAGCTGGGACTACCGACATACACTACTGCGCCTGGCTA T C PPP2R1B Ensembl:ENSG00000137713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs994378298 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_255,RMVar_hsa_circ_41061,RMVar_hsa_circ_59706,RMVar_hsa_circ_98866,RMVar_hsa_circ_153051,RMVar_hsa_circ_153052,RMVar_hsa_circ_350067,RMVar_hsa_circ_56575,RMVar_hsa_circ_48966,RMVar_hsa_circ_339137,RMVar_hsa_circ_32432,RMVar_hsa_circ_350302,RMVar_hsa_circ_22635,RMVar_hsa_circ_304491 31876 RMVar_ID_31876 Human_SNP_ID_481904586 A-to-I Human chr11 - 111767611 111767611 111767611 GGAGTACAGTGGTGCGATCCTGGCTCACTGCAACCTCTGCCTCCCGGGCTCAAGCGATTCTCATG GGAGTACAGTGGTGCGATCCTGGCTCACTGCAGCCTCTGCCTCCCGGGCTCAAGCGATTCTCATG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1205553053 Functional Loss SNV dbSNP153 33..33 33 - - - 31877 RMVar_ID_31877 Human_SNP_ID_481908274 A-to-I Human chr11 - 111783375 111783375 111783375 CAGCTCACTGCAACCTCTGTCTCCCGGGTTCAAGCAATTCTCCTGCTTCAGCCTCCTGAGTAGCT CAGCTCACTGCAACCTCTGTCTCCCGGGTTCACGCAATTCTCCTGCTTCAGCCTCCTGAGTAGCT T G ALG9 Ensembl:ENSG00000086848 Protein coding 3'UTR GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs1243927787 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11522824 31878 RMVar_ID_31878 Human_SNP_ID_481913337 A-to-I Human chr11 - 111806001 111806001 111806001 ACAAAAAAAATTAGCTGGCTATGGTGGTGAGCACCTATAGTCCCAGCTACACAGGAGGCTGAGAC ACAAAAAAAATTAGCTGGCTATGGTGGTGAGCCCCTATAGTCCCAGCTACACAGGAGGCTGAGAC T G AP001781.2,ALG9 Ensembl:ENSG00000258529,Ensembl:ENSG00000086848 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1168770854 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40805,RMVar_hsa_circ_153061,RMVar_hsa_circ_57394 31879 RMVar_ID_31879 Human_SNP_ID_481925536 A-to-I Human chr11 - 111858015 111858015 111858015 AGAGAATCGCTTGAACCAGGGAATCAGGTTGCAGTGAGCTGAGATCCCACCACTGCACTCCAGCC AGAGAATCGCTTGAACCAGGGAATCAGGTTGCGGTGAGCTGAGATCCCACCACTGCACTCCAGCC T C AP001781.2,ALG9 Ensembl:ENSG00000258529,Ensembl:ENSG00000086848 Protein coding,Protein coding intron,intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1299106877 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7514,RMVar_hsa_circ_39459,RMVar_hsa_circ_49665,RMVar_hsa_circ_336637,RMVar_hsa_circ_346339,RMVar_hsa_circ_118657,RMVar_hsa_circ_1135,RMVar_hsa_circ_36044,RMVar_hsa_circ_153069,RMVar_hsa_circ_153070,RMVar_hsa_circ_153068,RMVar_hsa_circ_14895,RMVar_hsa_circ_23729,RMVar_hsa_circ_299833,RMVar_hsa_circ_153073,RMVar_hsa_circ_294145 31880 RMVar_ID_31880 Human_SNP_ID_481925596 A-to-I Human chr11 - 111858207 111858207 111858207 GGAGAGGCCAGGTGCGGTGGTTCACGCCTGTAATCCCGGTACTTTGGGAGGTCGAGACAGGCAGA GGAGAGGCCAGGTGCGGTGGTTCACGCCTGTAGTCCCGGTACTTTGGGAGGTCGAGACAGGCAGA T C AP001781.2,ALG9 Ensembl:ENSG00000258529,Ensembl:ENSG00000086848 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1400119434 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7514,RMVar_hsa_circ_39459,RMVar_hsa_circ_49665,RMVar_hsa_circ_336637,RMVar_hsa_circ_346339,RMVar_hsa_circ_118657,RMVar_hsa_circ_1135,RMVar_hsa_circ_36044,RMVar_hsa_circ_153069,RMVar_hsa_circ_153070,RMVar_hsa_circ_153068,RMVar_hsa_circ_14895,RMVar_hsa_circ_23729,RMVar_hsa_circ_299833,RMVar_hsa_circ_153073,RMVar_hsa_circ_294145 31881 RMVar_ID_31881 Human_SNP_ID_481925741 A-to-I Human chr11 - 111858948 111858948 111858948 CCCACACCTTGGCCTCCCAGAGTACTGAGATTAAAGACATGAGCCACTGTGCCTGGCCTGCTACT CCCACACCTTGGCCTCCCAGAGTACTGAGATTGAAGACATGAGCCACTGTGCCTGGCCTGCTACT T C AP001781.2,ALG9 Ensembl:ENSG00000258529,Ensembl:ENSG00000086848 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1196384301 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11523065 RMVar_hsa_circ_7514,RMVar_hsa_circ_39459,RMVar_hsa_circ_49665,RMVar_hsa_circ_336637,RMVar_hsa_circ_346339,RMVar_hsa_circ_118657,RMVar_hsa_circ_1135,RMVar_hsa_circ_36044,RMVar_hsa_circ_153069,RMVar_hsa_circ_153070,RMVar_hsa_circ_153068,RMVar_hsa_circ_14895,RMVar_hsa_circ_23729,RMVar_hsa_circ_299833,RMVar_hsa_circ_153073,RMVar_hsa_circ_294145 31882 RMVar_ID_31882 Human_SNP_ID_481925815 A-to-I Human chr11 - 111859247 111859247 111859247 CACCCGCCTCAGTCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCACGTGGCCTCTTTTC CACCCGCCTCAGTCTCCCAAAGTGCTGGGATTTCAGGTGTGAGCCACCGCACGTGGCCTCTTTTC T A AP001781.2,ALG9 Ensembl:ENSG00000258529,Ensembl:ENSG00000086848 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1166293709 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7514,RMVar_hsa_circ_39459,RMVar_hsa_circ_49665,RMVar_hsa_circ_336637,RMVar_hsa_circ_346339,RMVar_hsa_circ_118657,RMVar_hsa_circ_1135,RMVar_hsa_circ_36044,RMVar_hsa_circ_153069,RMVar_hsa_circ_153070,RMVar_hsa_circ_153068,RMVar_hsa_circ_14895,RMVar_hsa_circ_23729,RMVar_hsa_circ_299833,RMVar_hsa_circ_153073,RMVar_hsa_circ_294145 31883 RMVar_ID_31883 Human_SNP_ID_481925816 A-to-I Human chr11 - 111859247 111859247 111859247 CACCCGCCTCAGTCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCACGTGGCCTCTTTTC CACCCGCCTCAGTCTCCCAAAGTGCTGGGATTCCAGGTGTGAGCCACCGCACGTGGCCTCTTTTC T G AP001781.2,ALG9 Ensembl:ENSG00000258529,Ensembl:ENSG00000086848 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1166293709 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7514,RMVar_hsa_circ_39459,RMVar_hsa_circ_49665,RMVar_hsa_circ_336637,RMVar_hsa_circ_346339,RMVar_hsa_circ_118657,RMVar_hsa_circ_1135,RMVar_hsa_circ_36044,RMVar_hsa_circ_153069,RMVar_hsa_circ_153070,RMVar_hsa_circ_153068,RMVar_hsa_circ_14895,RMVar_hsa_circ_23729,RMVar_hsa_circ_299833,RMVar_hsa_circ_153073,RMVar_hsa_circ_294145 31884 RMVar_ID_31884 Human_SNP_ID_481928457 A-to-I Human chr11 - 111870314 111870314 111870314 AGTCTGGGCACCTGAAGGATCTACTGCTTTCAAGTGTCTGCTTTCAGCAAGGTTATGTGCTGCTC AGTCTGGGCACCTGAAGGATCTACTGCTTTCAGGTGTCTGCTTTCAGCAAGGTTATGTGCTGCTC T C AP001781.2,ALG9 Ensembl:ENSG00000258529,Ensembl:ENSG00000086848 Protein coding,Protein coding CDS,CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs781991188 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1296888,Human_Splice_Rec_1296889,Human_Splice_Rec_1296920,Human_Splice_Rec_1296921,Human_Splice_Rec_1296986,Human_Splice_Rec_1296987,Human_Splice_Rec_1297014,Human_Splice_Rec_1297015,Human_Splice_Rec_1297056,Human_Splice_Rec_1297057,Human_Splice_Rec_1297090,Human_Splice_Rec_1297091,Human_Splice_Rec_1297104,Human_Splice_Rec_1297105,Human_Splice_Rec_1297114,Human_Splice_Rec_1297115,Human_Splice_Rec_1297126,Human_Splice_Rec_1297127,Human_Splice_Rec_1297154,Human_Splice_Rec_1297155,Human_Splice_Rec_1297166 Human_miRNA_ID_1376829,Human_miRNA_ID_1376830,Human_miRNA_ID_2402343,Human_miRNA_ID_2402344,Human_miRNA_ID_2701070,Human_miRNA_ID_2701071 RMVar_hsa_circ_49665,RMVar_hsa_circ_118657,RMVar_hsa_circ_153070,RMVar_hsa_circ_23729,RMVar_hsa_circ_153077,RMVar_hsa_circ_11563,RMVar_hsa_circ_323769 31885 RMVar_ID_31885 Human_SNP_ID_481934069 A-to-I Human chr11 - 111889375 111889375 111889375 AAATGGTGAAGGAAATTGAAATCAGCCAGCACACCAAGTACACTTGCTCTTTCTGTGGCAAAACC AAATGGTGAAGGAAATTGAAATCAGCCAGCACGCCAAGTACACTTGCTCTTTCTGTGGCAAAACC T C RPL37AP8 Ensembl:ENSG00000176343 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1197182391 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_388802,Human_RBP_ID_6109954,Human_RBP_ID_8998213 31886 RMVar_ID_31886 Human_SNP_ID_481957387 A-to-I Human chr11 + 111987840 111987840 111987840 CGCCACCATACCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACTATGTTGGCCAGGC CGCCACCATACCTGGCTAATTTTTGTATTTTTTGTAGAGATGGGGTTTCACTATGTTGGCCAGGC A T DIXDC1 Ensembl:ENSG00000150764 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1555174054 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102963,RMVar_hsa_circ_33757,RMVar_hsa_circ_153079,RMVar_hsa_circ_153080 31887 RMVar_ID_31887 Human_SNP_ID_481967804 A-to-I Human chr11 - 112029950 112029950 112029950 CTAAGTGTGATTGGCTGGATGGGAAGCATGTAATGTTTGGAAAAATCACTGATGGACTTCTAGTG CTAAGTGTGATTGGCTGGATGGGAAGCATGTAGTGTTTGGAAAAATCACTGATGGACTTCTAGTG T C PPIHP1 Ensembl:ENSG00000230911 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1286968460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1125600 31888 RMVar_ID_31888 Human_SNP_ID_481967805 A-to-I Human chr11 - 112029951 112029951 112029951 TCTAAGTGTGATTGGCTGGATGGGAAGCATGTAATGTTTGGAAAAATCACTGATGGACTTCTAGT TCTAAGTGTGATTGGCTGGATGGGAAGCATGTTATGTTTGGAAAAATCACTGATGGACTTCTAGT T A PPIHP1 Ensembl:ENSG00000230911 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1445081013 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1125600 31889 RMVar_ID_31889 Human_SNP_ID_481967806 A-to-I Human chr11 - 112029951 112029951 112029951 TCTAAGTGTGATTGGCTGGATGGGAAGCATGTAATGTTTGGAAAAATCACTGATGGACTTCTAGT TCTAAGTGTGATTGGCTGGATGGGAAGCATGTGATGTTTGGAAAAATCACTGATGGACTTCTAGT T C PPIHP1 Ensembl:ENSG00000230911 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1445081013 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1125600 31890 RMVar_ID_31890 Human_SNP_ID_481976300 A-to-I Human chr11 - 112065841 112065841 112065841 CAGTAGCTGGGATTACAGGCGACTGCCACCACACCCAGCTAAATTTTGCATTTTCAGTAGAGACT CAGTAGCTGGGATTACAGGCGACTGCCACCACGCCCAGCTAAATTTTGCATTTTCAGTAGAGACT T C PIH1D2 Ensembl:ENSG00000150773 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1429497616 Functional Loss SNV dbSNP153 33..33 33 - - - 31891 RMVar_ID_31891 Human_SNP_ID_481976560 A-to-I Human chr11 - 112066897 112066896 112066898 CACCACGCCTGGCTAGTTTTTGCATTTTTAGTAGAGAAAGGGTTTCACCATGTTGGCCAGGCTGG CACCACGCCTGGCTAGTTTTTGCATTTTTAG__GAGAAAGGGTTTCACCATGTTGGCCAGGCTGG CTA C PIH1D2 Ensembl:ENSG00000150773 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202576543 Functional Loss DEL dbSNP153 32..33 33 - - - 31892 RMVar_ID_31892 Human_SNP_ID_481977069 A-to-I Human chr11 - 112068566 112068566 112068566 TTGCCCATGTTGGTCTCGAACTCCTGGCCTCAAGTGATCCACCTGCCCTCAGCCTCCCAAAGTGC TTGCCCATGTTGGTCTCGAACTCCTGGCCTCATGTGATCCACCTGCCCTCAGCCTCCCAAAGTGC T A PIH1D2 Ensembl:ENSG00000150773 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1566652589 Functional Loss SNV dbSNP153 33..33 33 - - - 31893 RMVar_ID_31893 Human_SNP_ID_481977080 A-to-I Human chr11 - 112068621 112068621 112068621 TGCCACCAAGCCTGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTTGCCATGTTGCCCATGT TGCCACCAAGCCTGGCTAATTTTTGTATTTTTGGTAGAGACGGGGTTTTGCCATGTTGCCCATGT T C PIH1D2 Ensembl:ENSG00000150773 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs938932120 Functional Loss SNV dbSNP153 33..33 33 - - - 31894 RMVar_ID_31894 Human_SNP_ID_481977108 A-to-I Human chr11 - 112068732 112068732 112068732 TTGCCCAGGCTGGAGTGCAGTGGCACCATCTCAGCTTACTGCAACCTCTGCCTCCCAGGTTAAAG TTGCCCAGGCTGGAGTGCAGTGGCACCATCTCGGCTTACTGCAACCTCTGCCTCCCAGGTTAAAG T C PIH1D2 Ensembl:ENSG00000150773 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs587684991 Functional Loss SNV dbSNP153 33..33 33 - - - 31895 RMVar_ID_31895 Human_SNP_ID_481983654 A-to-I Human chr11 + 112093171 112093171 112093171 TTACTGCAACCTCCGCCTTTCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGCA TTACTGCAACCTCCGCCTTTCGGGTTCAAGCGGTTCTCCTGCCTCAGCCTCCCAAGTAGCTGGCA A G AP002884.2,SDHD Ensembl:ENSG00000255292,Ensembl:ENSG00000204370 Protein coding,Protein coding intron,CDS GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1467976831 Functional Loss SNV dbSNP153 33..33 33 - - - 31896 RMVar_ID_31896 Human_SNP_ID_481983703 A-to-I Human chr11 + 112093326 112093326 112093326 AACATCAGGTGATCCGCCCACTTCACCCACCCAAAGTGCTGGGATTACAGGTGTGAGCCACCACG AACATCAGGTGATCCGCCCACTTCACCCACCCCAAGTGCTGGGATTACAGGTGTGAGCCACCACG A C AP002884.2,SDHD Ensembl:ENSG00000255292,Ensembl:ENSG00000204370 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs912665859 Functional Loss SNV dbSNP153 33..33 33 - - - 31897 RMVar_ID_31897 Human_SNP_ID_481993048 A-to-I Human chr11 + 112131519 112131519 112131519 CCCTCATTTCTGTTTGCTGGGAAAGCCTGGCCAACGTGGTGAAAACCCATCTCTACTAAAAATAC CCCTCATTTCTGTTTGCTGGGAAAGCCTGGCCGACGTGGTGAAAACCCATCTCTACTAAAAATAC A G AP002884.2 Ensembl:ENSG00000255292 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs566345416 Functional Loss SNV dbSNP153 33..33 33 - - - 31898 RMVar_ID_31898 Human_SNP_ID_482000440 A-to-I Human chr11 - 112161737 112161737 112161737 GGAGTGCAGTGGCACGAACTCGGCTCACTGCAACCTCTGCCTCATGGGTTCAATCAGTTATTCTG GGAGTGCAGTGGCACGAACTCGGCTCACTGCAGCCTCTGCCTCATGGGTTCAATCAGTTATTCTG T C IL18 Ensembl:ENSG00000150782 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs990544931 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121433,RMVar_hsa_circ_153103 31899 RMVar_ID_31899 Human_SNP_ID_482384872 A-to-I Human chr11 - 113754886 113754886 113754886 CTGTAATCCAAGAGCTTTGGAAGGCCACGGTAAGAGAATTGCTTGAGGCCAGGAATTTGGGTAAC CTGTAATCCAAGAGCTTTGGAAGGCCACGGTAGGAGAATTGCTTGAGGCCAGGAATTTGGGTAAC T C ZW10 Ensembl:ENSG00000086827 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1287104140 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_377292,RMVar_hsa_circ_4163,RMVar_hsa_circ_51359,RMVar_hsa_circ_326124,RMVar_hsa_circ_310249,RMVar_hsa_circ_153143,RMVar_hsa_circ_64251,RMVar_hsa_circ_153145,RMVar_hsa_circ_115213,RMVar_hsa_circ_15947 31900 RMVar_ID_31900 Human_SNP_ID_482388844 A-to-I Human chr11 - 113771796 113771796 113771796 GGCGTGGTGGTGTGCGCCTGTAATCCCCAGCTACTCTGGAGGCTGAGGCAGGAGGATCGTTTGAA GGCGTGGTGGTGTGCGCCTGTAATCCCCAGCTGCTCTGGAGGCTGAGGCAGGAGGATCGTTTGAA T C ZW10 Ensembl:ENSG00000086827 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1565290375 Functional Loss SNV dbSNP153 33..33 33 - - - 31901 RMVar_ID_31901 Human_SNP_ID_482395471 A-to-I Human chr11 - 113798303 113798303 113798303 TCAAGTGATTCTCGTGCCTCAGCCTCCCGAATAGCTGGAATTACGGGCATGCACCACCACACCTG TCAAGTGATTCTCGTGCCTCAGCCTCCCGAATGGCTGGAATTACGGGCATGCACCACCACACCTG T C USP28 Ensembl:ENSG00000048028 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs540387028 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24868268 31902 RMVar_ID_31902 Human_SNP_ID_482398948 A-to-I Human chr11 - 113811686 113811686 113811686 AATAACTAAATTTTTTCTTTCTTTTTTTTTTGAGACATAGTCTTGCTTTGTCGCCCAGGCTGGAG AATAACTAAATTTTTTCTTTCTTTTTTTTTTGTGACATAGTCTTGCTTTGTCGCCCAGGCTGGAG T A USP28 Ensembl:ENSG00000048028 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs545837129 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51523,RMVar_hsa_circ_80792,RMVar_hsa_circ_345301,RMVar_hsa_circ_126506,RMVar_hsa_circ_153153,RMVar_hsa_circ_153154,RMVar_hsa_circ_53457,RMVar_hsa_circ_268351,RMVar_hsa_circ_127491,RMVar_hsa_circ_8966,RMVar_hsa_circ_5784,RMVar_hsa_circ_153156,RMVar_hsa_circ_294494,RMVar_hsa_circ_153158,RMVar_hsa_circ_309919,RMVar_hsa_circ_317880,RMVar_hsa_circ_339636,RMVar_hsa_circ_153160 31903 RMVar_ID_31903 Human_SNP_ID_482400761 A-to-I Human chr11 - 113818739 113818739 113818739 CTCCTGCCTCAGCCTCCCAAGGAGCTGGGACTACAGGAGTGTGCCATCATGCCTGGCTAATTTTT CTCCTGCCTCAGCCTCCCAAGGAGCTGGGACTGCAGGAGTGTGCCATCATGCCTGGCTAATTTTT T C USP28 Ensembl:ENSG00000048028 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs959131995 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51523,RMVar_hsa_circ_80792,RMVar_hsa_circ_345301,RMVar_hsa_circ_153154,RMVar_hsa_circ_53457,RMVar_hsa_circ_268351,RMVar_hsa_circ_127491,RMVar_hsa_circ_8966,RMVar_hsa_circ_153156,RMVar_hsa_circ_294494,RMVar_hsa_circ_153158,RMVar_hsa_circ_317880,RMVar_hsa_circ_153160,RMVar_hsa_circ_326541,RMVar_hsa_circ_24419,RMVar_hsa_circ_293579,RMVar_hsa_circ_70355,RMVar_hsa_circ_120933,RMVar_hsa_circ_153164,RMVar_hsa_circ_153163,RMVar_hsa_circ_318827,RMVar_hsa_circ_153166 31904 RMVar_ID_31904 Human_SNP_ID_482400772 A-to-I Human chr11 - 113818785 113818785 113818785 ATGATCTTGGCTCACTGTAGTCTCAACCTCCCAGGCTCAAGCGATCCTCCTGCCTCAGCCTCCCA ATGATCTTGGCTCACTGTAGTCTCAACCTCCCGGGCTCAAGCGATCCTCCTGCCTCAGCCTCCCA T C USP28 Ensembl:ENSG00000048028 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350003016 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51523,RMVar_hsa_circ_80792,RMVar_hsa_circ_345301,RMVar_hsa_circ_153154,RMVar_hsa_circ_53457,RMVar_hsa_circ_268351,RMVar_hsa_circ_127491,RMVar_hsa_circ_8966,RMVar_hsa_circ_153156,RMVar_hsa_circ_294494,RMVar_hsa_circ_153158,RMVar_hsa_circ_317880,RMVar_hsa_circ_153160,RMVar_hsa_circ_326541,RMVar_hsa_circ_24419,RMVar_hsa_circ_293579,RMVar_hsa_circ_70355,RMVar_hsa_circ_120933,RMVar_hsa_circ_153164,RMVar_hsa_circ_153163,RMVar_hsa_circ_318827,RMVar_hsa_circ_153166 31905 RMVar_ID_31905 Human_SNP_ID_482400945 A-to-I Human chr11 - 113819392 113819392 113819392 AATAAAAATGTTGGCCAGGCACAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGT AATAAAAATGTTGGCCAGGCACAGTGGCTCACTCCTGTAATCCCAGCACTTTGGGAGGCTGAGGT T A USP28 Ensembl:ENSG00000048028 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs927987463 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51523,RMVar_hsa_circ_80792,RMVar_hsa_circ_345301,RMVar_hsa_circ_153154,RMVar_hsa_circ_53457,RMVar_hsa_circ_268351,RMVar_hsa_circ_127491,RMVar_hsa_circ_8966,RMVar_hsa_circ_153156,RMVar_hsa_circ_294494,RMVar_hsa_circ_153158,RMVar_hsa_circ_317880,RMVar_hsa_circ_153160,RMVar_hsa_circ_326541,RMVar_hsa_circ_24419,RMVar_hsa_circ_293579,RMVar_hsa_circ_70355,RMVar_hsa_circ_120933,RMVar_hsa_circ_153164,RMVar_hsa_circ_153163,RMVar_hsa_circ_318827,RMVar_hsa_circ_153166 31906 RMVar_ID_31906 Human_SNP_ID_482528461 A-to-I Human chr11 + 114324632 114324631 114324632 ATTTAGGTTGGTTCCCTGTCTTTGCTATTGTGAATACTGCTGCAATGAACATTCTCATGCATGTC ATTTAGGTTGGTTCCCTGTCTTTGCTATTGTG_ATACTGCTGCAATGAACATTCTCATGCATGTC GA G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1254105161 Functional Loss DEL dbSNP153 33..33 33 - - - 31907 RMVar_ID_31907 Human_SNP_ID_482528463 A-to-I Human chr11 + 114324635 114324635 114324635 TAGGTTGGTTCCCTGTCTTTGCTATTGTGAATACTGCTGCAATGAACATTCTCATGCATGTCTTT TAGGTTGGTTCCCTGTCTTTGCTATTGTGAATGCTGCTGCAATGAACATTCTCATGCATGTCTTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs987170250 Functional Loss SNV dbSNP153 33..33 33 - - - 31908 RMVar_ID_31908 Human_SNP_ID_482590892 A-to-I Human chr11 + 114583541 114583541 114583541 AGCACAGCAAGCGGATGCAGAGATTCAACGTTAGTGAGGACTGTCCAGCATTTGATGGCCTGTTT AGCACAGCAAGCGGATGCAGAGATTCAACGTTCGTGAGGACTGTCCAGCATTTGATGGCCTGTTT A C AC020549.2 Ensembl:ENSG00000256674 Pseudogene exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs549768421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1817692,Human_miRNA_ID_1909414 31909 RMVar_ID_31909 Human_SNP_ID_482590893 A-to-I Human chr11 + 114583541 114583541 114583541 AGCACAGCAAGCGGATGCAGAGATTCAACGTTAGTGAGGACTGTCCAGCATTTGATGGCCTGTTT AGCACAGCAAGCGGATGCAGAGATTCAACGTTGGTGAGGACTGTCCAGCATTTGATGGCCTGTTT A G AC020549.2 Ensembl:ENSG00000256674 Pseudogene exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs549768421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1817692,Human_miRNA_ID_1909414 31910 RMVar_ID_31910 Human_SNP_ID_482743465 A-to-I Human chr11 - 115174943 115174943 115174943 CATATCTTAGATGGGGAGCCTCGGGAAAAGGTAGAGGAGTCACGTTACCATTTACATGTTTTAAA CATATCTTAGATGGGGAGCCTCGGGAAAAGGTGGAGGAGTCACGTTACCATTTACATGTTTTAAA T C CADM1 Ensembl:ENSG00000182985 Protein coding intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs564214197 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6045122,Human_RBP_ID_17230932,Human_RBP_ID_17462967 Human_miRNA_ID_644392,Human_miRNA_ID_1656414 31911 RMVar_ID_31911 Human_SNP_ID_482818590 A-to-I Human chr11 - 115486548 115486548 115486548 TTGAGCCCAGGAGCTTGAGACCAGCCTGGGCAACATAGTGAGACCCCGTCTCTACAAGAAATAAA TTGAGCCCAGGAGCTTGAGACCAGCCTGGGCAGCATAGTGAGACCCCGTCTCTACAAGAAATAAA T C CADM1 Ensembl:ENSG00000182985 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs558818126 Functional Loss SNV dbSNP153 33..33 33 - - - 31912 RMVar_ID_31912 Human_SNP_ID_483140416 A-to-I Human chr11 - 116751463 116751463 116751463 CACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGG CACCACGCCCAGCTAATTTTTGTATTTTTAGTGGAGACAGGGTTTCACCATGTTGGCCAGGCTGG T C BUD13 Ensembl:ENSG00000137656 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1050010020 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98925,RMVar_hsa_circ_106614,RMVar_hsa_circ_153212,RMVar_hsa_circ_98419,RMVar_hsa_circ_153213,RMVar_hsa_circ_153211 31913 RMVar_ID_31913 Human_SNP_ID_483166280 A-to-I Human chr11 - 116844706 116844703 116844707 TGCTATAAAAAGGATTGTTTCTCCATATATATATTATATATGTGTGTATATATATAATATAATAT TGCTATAAAAAGGATTGTTTCTCCATATATA____ATATATGTGTGTATATATATAATATAATAT TAATA T SIK3 Ensembl:ENSG00000160584 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1333666614 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_6047102,Human_RBP_ID_17790381,Human_RBP_ID_18175911,Human_RBP_ID_27614891 31914 RMVar_ID_31914 Human_SNP_ID_483207769 A-to-I Human chr11 - 117014724 117014724 117014724 AAAGAATGTTCTTCATGTTAATTGGTTAGGTTATGGTAATCATTGCATAATGTATACATCTATCA AAAGAATGTTCTTCATGTTAATTGGTTAGGTTGTGGTAATCATTGCATAATGTATACATCTATCA T C SIK3 Ensembl:ENSG00000160584 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1012528970 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97133,RMVar_hsa_circ_153238,RMVar_hsa_circ_153253 31915 RMVar_ID_31915 Human_SNP_ID_483207770 A-to-I Human chr11 - 117014729 117014729 117014729 AATGAAAAGAATGTTCTTCATGTTAATTGGTTAGGTTATGGTAATCATTGCATAATGTATACATC AATGAAAAGAATGTTCTTCATGTTAATTGGTTTGGTTATGGTAATCATTGCATAATGTATACATC T A SIK3 Ensembl:ENSG00000160584 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1197641986 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97133,RMVar_hsa_circ_153238,RMVar_hsa_circ_153253 31916 RMVar_ID_31916 Human_SNP_ID_483207776 A-to-I Human chr11 - 117014853 117014806 117014854 TGCCATGTTGCCCAGGCTGGTCTCAAACTCCTAGGCTCAAGCCATTCACCTGCCTCGGCCTCCTA TGCCATGTTGCCCAGGCTGGTCTCAAACTCC__________________________________ TGGAATCTCTCACTTTAGGAGGCCGAGGCAGGTGAATGGCTTGAGCCTA T SIK3 Ensembl:ENSG00000160584 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1228465406 Functional Loss DEL dbSNP153 32..65 33 - - - RMVar_hsa_circ_97133,RMVar_hsa_circ_153238,RMVar_hsa_circ_153253 31917 RMVar_ID_31917 Human_SNP_ID_483210707 A-to-I Human chr11 - 117024864 117024864 117024864 AGGGTCTCACTCTGTCACTCAGGCTAGAGTGCAGTGGCGCTGATCTCAGCTCTCTGCAACCTCCG AGGGTCTCACTCTGTCACTCAGGCTAGAGTGCGGTGGCGCTGATCTCAGCTCTCTGCAACCTCCG T C SIK3 Ensembl:ENSG00000160584 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1039464327 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11761873 RMVar_hsa_circ_97133,RMVar_hsa_circ_153238,RMVar_hsa_circ_153253 31918 RMVar_ID_31918 Human_SNP_ID_483211761 A-to-I Human chr11 - 117029335 117029335 117029335 CTTCCACCTCAGCCTCCTAAGTAGCTGGGACTATAGGTGCTTGCCACCATGCCCAGCTAATTTTT CTTCCACCTCAGCCTCCTAAGTAGCTGGGACTGTAGGTGCTTGCCACCATGCCCAGCTAATTTTT T C SIK3 Ensembl:ENSG00000160584 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1209683836 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97133,RMVar_hsa_circ_153238,RMVar_hsa_circ_153253 31919 RMVar_ID_31919 Human_SNP_ID_483223232 A-to-I Human chr11 - 117077034 117077034 117077034 CTCCCATCTCAGTTTCCTGAATAGCTAGGACTACAGACACACACCATTGCACTTGGCTAGTGGTT CTCCCATCTCAGTTTCCTGAATAGCTAGGACTGCAGACACACACCATTGCACTTGGCTAGTGGTT T C SIK3 Ensembl:ENSG00000160584 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1238361311 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2252247,Human_RBP_ID_11532815,Human_RBP_ID_17560162 RMVar_hsa_circ_97133,RMVar_hsa_circ_153238 31920 RMVar_ID_31920 Human_SNP_ID_483223234 A-to-I Human chr11 - 117077040 117077040 117077040 GTGATCCTCCCATCTCAGTTTCCTGAATAGCTAGGACTACAGACACACACCATTGCACTTGGCTA GTGATCCTCCCATCTCAGTTTCCTGAATAGCTTGGACTACAGACACACACCATTGCACTTGGCTA T A SIK3 Ensembl:ENSG00000160584 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1308240934 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11532815,Human_RBP_ID_17560162 RMVar_hsa_circ_97133,RMVar_hsa_circ_153238 31921 RMVar_ID_31921 Human_SNP_ID_483223243 A-to-I Human chr11 - 117077087 117077087 117077087 GTGTGGTGTGATTGTAGCTCACAGTCACCTCAAACTCCTGGGCTCAAGTGATCCTCCCATCTCAG GTGTGGTGTGATTGTAGCTCACAGTCACCTCAGACTCCTGGGCTCAAGTGATCCTCCCATCTCAG T C SIK3 Ensembl:ENSG00000160584 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749268516 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97133,RMVar_hsa_circ_153238 31922 RMVar_ID_31922 Human_SNP_ID_483225092 A-to-I Human chr11 - 117085185 117085177 117085186 TTGAGCCCAGGAGTTCCAGATTACAGTGCAGTAAACTATGGTTGCGCCACTGCATTCCAGCCTGT TTGAGCCCAGGAGTTCCAGATTACAGTGCAG_________GTTGCGCCACTGCATTCCAGCCTGT CCATAGTTTA C SIK3 Ensembl:ENSG00000160584 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 29129909,30559470 RNA-Seq:(High) rs1399856752 Functional Loss DEL dbSNP153 32..40 33 - - - Human_RBP_ID_11533019 RMVar_hsa_circ_97133,RMVar_hsa_circ_153238 31923 RMVar_ID_31923 Human_SNP_ID_483225095 A-to-I Human chr11 - 117085185 117085185 117085185 TTGAGCCCAGGAGTTCCAGATTACAGTGCAGTAAACTATGGTTGCGCCACTGCATTCCAGCCTGT TTGAGCCCAGGAGTTCCAGATTACAGTGCAGTGAACTATGGTTGCGCCACTGCATTCCAGCCTGT T C SIK3 Ensembl:ENSG00000160584 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 29129909,30559470 RNA-Seq:(High) rs1376684157 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11533019 RMVar_hsa_circ_97133,RMVar_hsa_circ_153238 31924 RMVar_ID_31924 Human_SNP_ID_483225223 A-to-I Human chr11 - 117085768 117085768 117085768 GTTGGCCAGGATGGTCTCGAATTCCTGAGCTCAGGCAGTTCGCCTGCTTCGGTCTCCTAAAGTGC GTTGGCCAGGATGGTCTCGAATTCCTGAGCTCGGGCAGTTCGCCTGCTTCGGTCTCCTAAAGTGC T C SIK3 Ensembl:ENSG00000160584 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs943786956 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97133,RMVar_hsa_circ_153238 31925 RMVar_ID_31925 Human_SNP_ID_483225978 A-to-I Human chr11 - 117088737 117088737 117088737 AGGAGGTCAAGGTTTCTGTGAGCTATGATCGCACCACTGAACTCCAGCCTGGGCAACAGAGCCAG AGGAGGTCAAGGTTTCTGTGAGCTATGATCGCTCCACTGAACTCCAGCCTGGGCAACAGAGCCAG T A SIK3 Ensembl:ENSG00000160584 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1389926983 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11533090 RMVar_hsa_circ_97133,RMVar_hsa_circ_153238 31926 RMVar_ID_31926 Human_SNP_ID_483227417 A-to-I Human chr11 - 117094532 117094532 117094532 ACTGCCAGAGTTCACTGTAACCTCCAACTCCCAGGCTCAAGAGATCCTCCTGCCTCAGCTTCCTA ACTGCCAGAGTTCACTGTAACCTCCAACTCCCGGGCTCAAGAGATCCTCCTGCCTCAGCTTCCTA T C SIK3 Ensembl:ENSG00000160584 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971944401 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97133,RMVar_hsa_circ_153238 31927 RMVar_ID_31927 Human_SNP_ID_483233712 A-to-I Human chr11 - 117117916 117117916 117117916 TGGCTCAACTTCAAGAAAAAGCCTTGTTTGCAATCTCTAAAAATTACAAGCTCATAGCTACACCA TGGCTCAACTTCAAGAAAAAGCCTTGTTTGCACTCTCTAAAAATTACAAGCTCATAGCTACACCA T G AP000936.2 Ensembl:ENSG00000225236 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs892466163 Functional Loss SNV dbSNP153 33..33 33 - - - 31928 RMVar_ID_31928 Human_SNP_ID_483241933 A-to-I Human chr11 + 117148654 117148654 117148654 TTATTGAATTGTAGCTCTAAGCTGGGAGTGGTAGTGTGTGCCTGTAGTCCCAGCTACTTGGGAAG TTATTGAATTGTAGCTCTAAGCTGGGAGTGGTGGTGTGTGCCTGTAGTCCCAGCTACTTGGGAAG A G PAFAH1B2 Ensembl:ENSG00000168092 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs929137997 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6047715 RMVar_hsa_circ_153254,RMVar_hsa_circ_96342,RMVar_hsa_circ_153255 31929 RMVar_ID_31929 Human_SNP_ID_483243937 A-to-I Human chr11 + 117155189 117155189 117155189 GTTGGTCAAGCCGGTCTTGAACTCCTGACCTCAGGTGATCCACGCACCTTAGCCTCCCAAAATGC GTTGGTCAAGCCGGTCTTGAACTCCTGACCTCGGGTGATCCACGCACCTTAGCCTCCCAAAATGC A G PAFAH1B2 Ensembl:ENSG00000168092 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1013660451 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122440,RMVar_hsa_circ_289605,RMVar_hsa_circ_153254,RMVar_hsa_circ_96342,RMVar_hsa_circ_376835,RMVar_hsa_circ_296124,RMVar_hsa_circ_268174,RMVar_hsa_circ_280906,RMVar_hsa_circ_127876,RMVar_hsa_circ_153257,RMVar_hsa_circ_153259,RMVar_hsa_circ_153260,RMVar_hsa_circ_153258,RMVar_hsa_circ_153256 31930 RMVar_ID_31930 Human_SNP_ID_483246735 A-to-I Human chr11 + 117164786 117164786 117164786 GGCCGGGTGTGGTGGCTCACGTCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGTGGATCACA GGCCGGGTGTGGTGGCTCACGTCTGTAATCCCGGCACTTTGGGAGGCCGAGGCGGGTGGATCACA A G PAFAH1B2 Ensembl:ENSG00000168092 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10892080 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105706,RMVar_hsa_circ_122440,RMVar_hsa_circ_153254,RMVar_hsa_circ_96342,RMVar_hsa_circ_376835,RMVar_hsa_circ_127876,RMVar_hsa_circ_153257,RMVar_hsa_circ_153256,RMVar_hsa_circ_112908,RMVar_hsa_circ_153264,RMVar_hsa_circ_153266,RMVar_hsa_circ_127205,RMVar_hsa_circ_153268 31931 RMVar_ID_31931 Human_SNP_ID_483246736 A-to-I Human chr11 + 117164786 117164786 117164786 GGCCGGGTGTGGTGGCTCACGTCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGTGGATCACA GGCCGGGTGTGGTGGCTCACGTCTGTAATCCCTGCACTTTGGGAGGCCGAGGCGGGTGGATCACA A T PAFAH1B2 Ensembl:ENSG00000168092 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10892080 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105706,RMVar_hsa_circ_122440,RMVar_hsa_circ_153254,RMVar_hsa_circ_96342,RMVar_hsa_circ_376835,RMVar_hsa_circ_127876,RMVar_hsa_circ_153257,RMVar_hsa_circ_153256,RMVar_hsa_circ_112908,RMVar_hsa_circ_153264,RMVar_hsa_circ_153266,RMVar_hsa_circ_127205,RMVar_hsa_circ_153268 31932 RMVar_ID_31932 Human_SNP_ID_483247139 A-to-I Human chr11 + 117165978 117165978 117165978 TCTTCTGCCTCAAATCCCAAGTAGCTGGAACTACAGGTGCATGCCACCATGCCCGGCTAATTTTT TCTTCTGCCTCAAATCCCAAGTAGCTGGAACTGCAGGTGCATGCCACCATGCCCGGCTAATTTTT A G PAFAH1B2 Ensembl:ENSG00000168092 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs916048156 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105706,RMVar_hsa_circ_122440,RMVar_hsa_circ_153254,RMVar_hsa_circ_96342,RMVar_hsa_circ_376835,RMVar_hsa_circ_127876,RMVar_hsa_circ_153257,RMVar_hsa_circ_153256,RMVar_hsa_circ_112908,RMVar_hsa_circ_153264,RMVar_hsa_circ_153266,RMVar_hsa_circ_127205,RMVar_hsa_circ_153268 31933 RMVar_ID_31933 Human_SNP_ID_483247906 A-to-I Human chr11 - 117168610 117168608 117168610 CCAGAACTCCGAATATGAACAGCAATACACAGAATCTATAGCACAGAACACCACACAAGAATGAG CCAGAACTCCGAATATGAACAGCAATACACAG__TCTATAGCACAGAACACCACACAAGAATGAG ATT A - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1433432232 Functional Loss DEL dbSNP153 33..34 33 - - - 31934 RMVar_ID_31934 Human_SNP_ID_483247909 A-to-I Human chr11 - 117168610 117168610 117168610 CCAGAACTCCGAATATGAACAGCAATACACAGAATCTATAGCACAGAACACCACACAAGAATGAG CCAGAACTCCGAATATGAACAGCAATACACAGCATCTATAGCACAGAACACCACACAAGAATGAG T G - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1159779270 Functional Loss SNV dbSNP153 33..33 33 - - - 31935 RMVar_ID_31935 Human_SNP_ID_483253262 A-to-I Human chr11 + 117185757 117185757 117185757 AAAATGAGCCAGGCGTGGTGGCACACATCTGTAGTCCCAGCTACTCAGGAGGCTGAGGTGGAAGG AAAATGAGCCAGGCGTGGTGGCACACATCTGTCGTCCCAGCTACTCAGGAGGCTGAGGTGGAAGG A C SIDT2 Ensembl:ENSG00000149577 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs998109827 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76696,RMVar_hsa_circ_153272,RMVar_hsa_circ_70990,RMVar_hsa_circ_84878,RMVar_hsa_circ_153273 31936 RMVar_ID_31936 Human_SNP_ID_483256750 A-to-I Human chr11 - 117197313 117197313 117197313 TCTCCCAGCCCTTCAAGCAGAGCTATAAAAACAAGTTTGGGAGAAAAACACATTCCCATCCCCAA TCTCCCAGCCCTTCAAGCAGAGCTATAAAAACGAGTTTGGGAGAAAAACACATTCCCATCCCCAA T C LOC100652768,LOC100652768:2,LOC100652768:3,LOC100652768:4,LOC100652768:5 RNACentral:URS000075AE67,RNACentral:URS00008B8348,RNACentral:URS00008B996D,RNACentral:URS00008B40F9,RNACentral:URS00008BB314 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,intron,intron,exon,exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1342749316 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92603,RMVar_hsa_circ_153284 31937 RMVar_ID_31937 Human_SNP_ID_483260813 A-to-I Human chr11 - 117210813 117210813 117210813 TCCCACCCTCAACCTCCTGAGTAGCTGGGACCACAGGTGCTTACCACTATATCCAGCTAATTTTT TCCCACCCTCAACCTCCTGAGTAGCTGGGACCGCAGGTGCTTACCACTATATCCAGCTAATTTTT T C PCSK7 Ensembl:ENSG00000160613 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs940922651 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99349,RMVar_hsa_circ_115938,RMVar_hsa_circ_106577,RMVar_hsa_circ_97461,RMVar_hsa_circ_114308,RMVar_hsa_circ_153287,RMVar_hsa_circ_153289,RMVar_hsa_circ_153288,RMVar_hsa_circ_153286,RMVar_hsa_circ_126610,RMVar_hsa_circ_153291,RMVar_hsa_circ_153292 31938 RMVar_ID_31938 Human_SNP_ID_483260822 A-to-I Human chr11 - 117210853 117210853 117210853 TGGTTCACTGCAGCCTCAACCTCCTGGGCTCAAGCCATCCTCCCACCCTCAACCTCCTGAGTAGC TGGTTCACTGCAGCCTCAACCTCCTGGGCTCAGGCCATCCTCCCACCCTCAACCTCCTGAGTAGC T C PCSK7 Ensembl:ENSG00000160613 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs748153004 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99349,RMVar_hsa_circ_115938,RMVar_hsa_circ_106577,RMVar_hsa_circ_97461,RMVar_hsa_circ_114308,RMVar_hsa_circ_153287,RMVar_hsa_circ_153289,RMVar_hsa_circ_153288,RMVar_hsa_circ_153286,RMVar_hsa_circ_126610,RMVar_hsa_circ_153291,RMVar_hsa_circ_153292 31939 RMVar_ID_31939 Human_SNP_ID_483260823 A-to-I Human chr11 - 117210854 117210854 117210854 ATGGTTCACTGCAGCCTCAACCTCCTGGGCTCAAGCCATCCTCCCACCCTCAACCTCCTGAGTAG ATGGTTCACTGCAGCCTCAACCTCCTGGGCTCGAGCCATCCTCCCACCCTCAACCTCCTGAGTAG T C PCSK7 Ensembl:ENSG00000160613 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388818739 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99349,RMVar_hsa_circ_115938,RMVar_hsa_circ_106577,RMVar_hsa_circ_97461,RMVar_hsa_circ_114308,RMVar_hsa_circ_153287,RMVar_hsa_circ_153289,RMVar_hsa_circ_153288,RMVar_hsa_circ_153286,RMVar_hsa_circ_126610,RMVar_hsa_circ_153291,RMVar_hsa_circ_153292 31940 RMVar_ID_31940 Human_SNP_ID_483260833 A-to-I Human chr11 - 117210879 117210879 117210879 CAGGCTAGAGTGCAGAGGCACAGTCATGGTTCACTGCAGCCTCAACCTCCTGGGCTCAAGCCATC CAGGCTAGAGTGCAGAGGCACAGTCATGGTTCTCTGCAGCCTCAACCTCCTGGGCTCAAGCCATC T A PCSK7 Ensembl:ENSG00000160613 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1166364328 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99349,RMVar_hsa_circ_115938,RMVar_hsa_circ_106577,RMVar_hsa_circ_97461,RMVar_hsa_circ_114308,RMVar_hsa_circ_153287,RMVar_hsa_circ_153289,RMVar_hsa_circ_153288,RMVar_hsa_circ_153286,RMVar_hsa_circ_126610,RMVar_hsa_circ_153291,RMVar_hsa_circ_153292 31941 RMVar_ID_31941 Human_SNP_ID_483260834 A-to-I Human chr11 - 117210879 117210879 117210879 CAGGCTAGAGTGCAGAGGCACAGTCATGGTTCACTGCAGCCTCAACCTCCTGGGCTCAAGCCATC CAGGCTAGAGTGCAGAGGCACAGTCATGGTTCGCTGCAGCCTCAACCTCCTGGGCTCAAGCCATC T C PCSK7 Ensembl:ENSG00000160613 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1166364328 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99349,RMVar_hsa_circ_115938,RMVar_hsa_circ_106577,RMVar_hsa_circ_97461,RMVar_hsa_circ_114308,RMVar_hsa_circ_153287,RMVar_hsa_circ_153289,RMVar_hsa_circ_153288,RMVar_hsa_circ_153286,RMVar_hsa_circ_126610,RMVar_hsa_circ_153291,RMVar_hsa_circ_153292 31942 RMVar_ID_31942 Human_SNP_ID_483260842 A-to-I Human chr11 - 117210905 117210905 117210905 TTGAGACAGGCTCTCACTCTATTGCCCAGGCTAGAGTGCAGAGGCACAGTCATGGTTCACTGCAG TTGAGACAGGCTCTCACTCTATTGCCCAGGCTGGAGTGCAGAGGCACAGTCATGGTTCACTGCAG T C PCSK7 Ensembl:ENSG00000160613 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs60584552 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99349,RMVar_hsa_circ_115938,RMVar_hsa_circ_106577,RMVar_hsa_circ_97461,RMVar_hsa_circ_114308,RMVar_hsa_circ_153287,RMVar_hsa_circ_153289,RMVar_hsa_circ_153288,RMVar_hsa_circ_153286,RMVar_hsa_circ_126610,RMVar_hsa_circ_153291,RMVar_hsa_circ_153292 31943 RMVar_ID_31943 Human_SNP_ID_483260845 A-to-I Human chr11 - 117210917 117210917 117210917 TAATTTTTTTTTTTGAGACAGGCTCTCACTCTATTGCCCAGGCTAGAGTGCAGAGGCACAGTCAT TAATTTTTTTTTTTGAGACAGGCTCTCACTCTGTTGCCCAGGCTAGAGTGCAGAGGCACAGTCAT T C PCSK7 Ensembl:ENSG00000160613 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs777435076 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99349,RMVar_hsa_circ_115938,RMVar_hsa_circ_106577,RMVar_hsa_circ_97461,RMVar_hsa_circ_114308,RMVar_hsa_circ_153287,RMVar_hsa_circ_153289,RMVar_hsa_circ_153288,RMVar_hsa_circ_153286,RMVar_hsa_circ_126610,RMVar_hsa_circ_153291,RMVar_hsa_circ_153292 31944 RMVar_ID_31944 Human_SNP_ID_483268566 A-to-I Human chr11 + 117238215 117238208 117238216 GATGGATCCCTTGAGTACAGGAGTTCGAGACCAGCCTGGGCAACATGGCAAAACCGTGCAAAAAA GATGGATCCCTTGAGTACAGGAGTTC________CCTGGGCAACATGGCAAAACCGTGCAAAAAA CGAGACCAG C RNF214 Ensembl:ENSG00000167257 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1288834142 Functional Loss DEL dbSNP153 27..34 33 - - - RMVar_hsa_circ_90834,RMVar_hsa_circ_32638,RMVar_hsa_circ_45714,RMVar_hsa_circ_153297,RMVar_hsa_circ_24190 31945 RMVar_ID_31945 Human_SNP_ID_483271217 A-to-I Human chr11 + 117247420 117247420 117247420 GGGAGGCTGAGGTGGAAGAATCACTTGAGCCCAGGAGTTCCAGGCTGCAGTCAGCTGTGATTACG GGGAGGCTGAGGTGGAAGAATCACTTGAGCCCCGGAGTTCCAGGCTGCAGTCAGCTGTGATTACG A C RNF214 Ensembl:ENSG00000167257 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1233448313 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90834,RMVar_hsa_circ_153297,RMVar_hsa_circ_153300,RMVar_hsa_circ_360563 31946 RMVar_ID_31946 Human_SNP_ID_483271738 A-to-I Human chr11 + 117249139 117249139 117249139 TAGAGATGAGAATCTCACTCGTTGACCAGGCTAATCTCAAACTTCTGGCTTCAAGCGATCCACCT TAGAGATGAGAATCTCACTCGTTGACCAGGCTGATCTCAAACTTCTGGCTTCAAGCGATCCACCT A G RNF214 Ensembl:ENSG00000167257 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs547074279 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11534638 RMVar_hsa_circ_90834,RMVar_hsa_circ_153297,RMVar_hsa_circ_153300,RMVar_hsa_circ_360563 31947 RMVar_ID_31947 Human_SNP_ID_483272991 A-to-I Human chr11 + 117253061 117253061 117253061 TAGAAACAGGATCTCACTCTGTTGGCCCAGCTAGAGTGTAGTGGTACAGTCATGGCTCACTAAAG TAGAAACAGGATCTCACTCTGTTGGCCCAGCTGGAGTGTAGTGGTACAGTCATGGCTCACTAAAG A G RNF214 Ensembl:ENSG00000167257 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs536407485 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11534667 RMVar_hsa_circ_90834,RMVar_hsa_circ_153297,RMVar_hsa_circ_153300,RMVar_hsa_circ_360563 31948 RMVar_ID_31948 Human_SNP_ID_483273106 A-to-I Human chr11 + 117253586 117253586 117253586 TATTGTGTGCAGGTGCGATGGCTTATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGAGG TATTGTGTGCAGGTGCGATGGCTTATGCCTGTTATCCCAGCACTTTGGGAGGCCAAGGCGGGAGG A T RNF214 Ensembl:ENSG00000167257 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1398780832 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90834,RMVar_hsa_circ_153297,RMVar_hsa_circ_153300,RMVar_hsa_circ_360563 31949 RMVar_ID_31949 Human_SNP_ID_483275645 A-to-I Human chr11 + 117262833 117262833 117262833 AGCTCTTTTCTTTTCTTTTTTGTTTTTGAGACAGGGTGTTGCTCTGCCACCCAGGTTGAAGTGCA AGCTCTTTTCTTTTCTTTTTTGTTTTTGAGACTGGGTGTTGCTCTGCCACCCAGGTTGAAGTGCA A T RNF214 Ensembl:ENSG00000167257 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1182570238 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90834,RMVar_hsa_circ_153297,RMVar_hsa_circ_153300,RMVar_hsa_circ_360563 31950 RMVar_ID_31950 Human_SNP_ID_483282429 A-to-I Human chr11 - 117289283 117289283 117289283 TTAAGTCGGGAAATTCTGCTGCTTGAAACTTCAGCCCTGAACCTTTGTCCACCATTCCTTTAAAT TTAAGTCGGGAAATTCTGCTGCTTGAAACTTCCGCCCTGAACCTTTGTCCACCATTCCTTTAAAT T G BACE1 Ensembl:ENSG00000186318 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs555012044 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23488564,Human_RBP_ID_27409023 31951 RMVar_ID_31951 Human_SNP_ID_483290698 A-to-I Human chr11 + 117321772 117321768 117321773 CAGGCTGCAGTGCAGTGGCATGATCATGGCTCACTACAGCCTTGACCTCCTGTGCTCAAGTGACC CAGGCTGCAGTGCAGTGGCATGATCATGACTCATTACAGCCTTGACCTCCTGTGCTCAAGTGACC GCTCAC ACTCAT CEP164 Ensembl:ENSG00000110274 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs386757857 Functional Loss MNV dbSNP153 29..34 33 - - - RMVar_hsa_circ_153306,RMVar_hsa_circ_121788 31952 RMVar_ID_31952 Human_SNP_ID_483293283 A-to-I Human chr11 + 117332034 117332034 117332034 ATTTGTGGAGACAGGGTCTTACTATATTGCTCAGGCTGGTCTTGAGCTTCTAGGCTCAAGTGATC ATTTGTGGAGACAGGGTCTTACTATATTGCTCCGGCTGGTCTTGAGCTTCTAGGCTCAAGTGATC A C CEP164 Ensembl:ENSG00000110274 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs923232035 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_153306,RMVar_hsa_circ_121788,RMVar_hsa_circ_153307,RMVar_hsa_circ_105071 31953 RMVar_ID_31953 Human_SNP_ID_483293290 A-to-I Human chr11 + 117332059 117332059 117332059 ATTGCTCAGGCTGGTCTTGAGCTTCTAGGCTCAAGTGATCCTAGGCCTTGGTCCCCCATAGTATT ATTGCTCAGGCTGGTCTTGAGCTTCTAGGCTCGAGTGATCCTAGGCCTTGGTCCCCCATAGTATT A G CEP164 Ensembl:ENSG00000110274 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1344594483 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_153306,RMVar_hsa_circ_121788,RMVar_hsa_circ_153307,RMVar_hsa_circ_105071 31954 RMVar_ID_31954 Human_SNP_ID_483293576 A-to-I Human chr11 + 117333232 117333232 117333232 GACGGTCTCACTATGTTGACCCAGCTAGTCTCAAACTCCTGGCTTCAAGTGATCCTCCTGCTTTA GACGGTCTCACTATGTTGACCCAGCTAGTCTCCAACTCCTGGCTTCAAGTGATCCTCCTGCTTTA A C CEP164 Ensembl:ENSG00000110274 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053466782 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_153306,RMVar_hsa_circ_121788,RMVar_hsa_circ_153307,RMVar_hsa_circ_105071 31955 RMVar_ID_31955 Human_SNP_ID_483293578 A-to-I Human chr11 + 117333246 117333246 117333246 GTTGACCCAGCTAGTCTCAAACTCCTGGCTTCAAGTGATCCTCCTGCTTTAGCCTCCCAAAGCCC GTTGACCCAGCTAGTCTCAAACTCCTGGCTTCTAGTGATCCTCCTGCTTTAGCCTCCCAAAGCCC A T CEP164 Ensembl:ENSG00000110274 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893508173 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_153306,RMVar_hsa_circ_121788,RMVar_hsa_circ_153307,RMVar_hsa_circ_105071 31956 RMVar_ID_31956 Human_SNP_ID_483297529 A-to-I Human chr11 + 117349585 117349585 117349585 ATAGCTCACTGCAGCCTCGAACAGCTGGGCTCAAGGGATCCTCCTGCCTCAGCTTCCTAAGTGGC ATAGCTCACTGCAGCCTCGAACAGCTGGGCTCCAGGGATCCTCCTGCCTCAGCTTCCTAAGTGGC A C CEP164 Ensembl:ENSG00000110274 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs931225828 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17469,RMVar_hsa_circ_97860,RMVar_hsa_circ_153306,RMVar_hsa_circ_121788,RMVar_hsa_circ_153307,RMVar_hsa_circ_105071,RMVar_hsa_circ_321828,RMVar_hsa_circ_153310,RMVar_hsa_circ_378799,RMVar_hsa_circ_87554,RMVar_hsa_circ_153311,RMVar_hsa_circ_153312,RMVar_hsa_circ_153313,RMVar_hsa_circ_123191,RMVar_hsa_circ_342940,RMVar_hsa_circ_153314 31957 RMVar_ID_31957 Human_SNP_ID_483390018 A-to-I Human chr11 - 117713186 117713186 117713186 GCTTGAAGGCAGGAGAAATGCTTGAACCCAGAAGGTGGAGGTCGCAGTGAGCCGAGGTCATGCCG GCTTGAAGGCAGGAGAAATGCTTGAACCCAGAGGGTGGAGGTCGCAGTGAGCCGAGGTCATGCCG T C DSCAML1 Ensembl:ENSG00000177103 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs563923394 Functional Loss SNV dbSNP153 33..33 33 - - - 31958 RMVar_ID_31958 Human_SNP_ID_483554723 A-to-I Human chr11 + 118363870 118363870 118363870 GAACTCCTGACCTCAGGTGATCCACCTGCCTCAGCCTCCCAGGGTGCTGGGATTGCAGGCATGAG GAACTCCTGACCTCAGGTGATCCACCTGCCTCGGCCTCCCAGGGTGCTGGGATTGCAGGCATGAG A G UBE4A Ensembl:ENSG00000110344 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs564315059 Functional Loss SNV dbSNP153 33..33 33 - - - 31959 RMVar_ID_31959 Human_SNP_ID_483557315 A-to-I Human chr11 + 118374058 118374058 118374058 ATCACTTGAGCCTGGGAGGTCAAGACTTCAGTAAGCCATGATTGCATCATCACGCTCCGGCCTGG ATCACTTGAGCCTGGGAGGTCAAGACTTCAGTGAGCCATGATTGCATCATCACGCTCCGGCCTGG A G UBE4A Ensembl:ENSG00000110344 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs547284937 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61472,RMVar_hsa_circ_37813,RMVar_hsa_circ_95262,RMVar_hsa_circ_153344,RMVar_hsa_circ_323553,RMVar_hsa_circ_331887,RMVar_hsa_circ_354270,RMVar_hsa_circ_64227,RMVar_hsa_circ_153345,RMVar_hsa_circ_34211 31960 RMVar_ID_31960 Human_SNP_ID_483562061 A-to-I Human chr11 + 118393713 118393681 118393713 CGCCTCCCAGGATCAAGTGATTCTTCAGCCTCAGCCTCCCGAATAGCTGAGACTACAGGTGAGCA C________________________________GCCTCCCGAATAGCTGAGACTACAGGTGAGCA CGCCTCCCAGGATCAAGTGATTCTTCAGCCTCA C UBE4A Ensembl:ENSG00000110344 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1242414509 Functional Loss DEL dbSNP153 2..33 33 - - - 31961 RMVar_ID_31961 Human_SNP_ID_483562083 A-to-I Human chr11 + 118393798 118393798 118393798 TTGTATTTGTAATAGAGATGAGGTTTCACCATATTGGCCAGGCTGGTCTTAAACTCCTGATTTCA TTGTATTTGTAATAGAGATGAGGTTTCACCATGTTGGCCAGGCTGGTCTTAAACTCCTGATTTCA A G UBE4A Ensembl:ENSG00000110344 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1261332499 Functional Loss SNV dbSNP153 33..33 33 - - - 31962 RMVar_ID_31962 Human_SNP_ID_483562176 A-to-I Human chr11 + 118394217 118394217 118394217 CTTGCTCTGTCACCAGGCTGGAGTGCAGTGGCATGATCTCAGCTTACTGTGGCCTCACCCTCCCA CTTGCTCTGTCACCAGGCTGGAGTGCAGTGGCGTGATCTCAGCTTACTGTGGCCTCACCCTCCCA A G UBE4A Ensembl:ENSG00000110344 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1213870595 Functional Loss SNV dbSNP153 33..33 33 - - - 31963 RMVar_ID_31963 Human_SNP_ID_483562204 A-to-I Human chr11 + 118394371 118394371 118394371 TTTTGTAGAGAAGGGGTCTCTCCATGTTACCCAGGCCAGTCTCAAACTCCTGGGCTCAAGCAGTC TTTTGTAGAGAAGGGGTCTCTCCATGTTACCCCGGCCAGTCTCAAACTCCTGGGCTCAAGCAGTC A C UBE4A Ensembl:ENSG00000110344 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1482262646 Functional Loss SNV dbSNP153 33..33 33 - - - 31964 RMVar_ID_31964 Human_SNP_ID_483596021 A-to-I Human chr11 + 118536974 118536974 118536974 ATAGCTCACTGCAGCCTTGAACTCCTGTGTTCAAGGGATCCTCCCACCTCAGCCTCATGACTAGT ATAGCTCACTGCAGCCTTGAACTCCTGTGTTCTAGGGATCCTCCCACCTCAGCCTCATGACTAGT A T TMEM25 Ensembl:ENSG00000149582 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1555063704 Functional Loss SNV dbSNP153 33..33 33 - - - 31965 RMVar_ID_31965 Human_SNP_ID_483598446 A-to-I Human chr11 - 118546484 118546484 118546484 TTCCCTCCCTCCCTTCCTTCCTTTTTTTTTACAGGGTATTACTCTATGCCCAGGCTGGAGTGCAG TTCCCTCCCTCCCTTCCTTCCTTTTTTTTTACGGGGTATTACTCTATGCCCAGGCTGGAGTGCAG T C IFT46 Ensembl:ENSG00000118096 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1325310513 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_153400,RMVar_hsa_circ_117741 31966 RMVar_ID_31966 Human_SNP_ID_483605512 A-to-I Human chr11 + 118574860 118574860 118574860 GCTATCATAGTGCACTGCGGCCTAGAACTCCTAGCCTCAAGCAATCCTCCCGCCTCCATATCCCA GCTATCATAGTGCACTGCGGCCTAGAACTCCTGGCCTCAAGCAATCCTCCCGCCTCCATATCCCA A G ARCN1 Ensembl:ENSG00000095139 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1346289936 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11538409 RMVar_hsa_circ_112504,RMVar_hsa_circ_153407 31967 RMVar_ID_31967 Human_SNP_ID_483607530 A-to-I Human chr11 + 118582052 118582052 118582052 GCGGTAGCATGTGCCTGTAGTCCAAGCTACTCAGGAGGCTGAGGCAGAAGGATTGCTTGAGGCCA GCGGTAGCATGTGCCTGTAGTCCAAGCTACTCGGGAGGCTGAGGCAGAAGGATTGCTTGAGGCCA A G ARCN1 Ensembl:ENSG00000095139 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1160888431 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_153409,RMVar_hsa_circ_288469,RMVar_hsa_circ_112504,RMVar_hsa_circ_317410,RMVar_hsa_circ_347413,RMVar_hsa_circ_153407,RMVar_hsa_circ_324954,RMVar_hsa_circ_309969,RMVar_hsa_circ_153411,RMVar_hsa_circ_283063,RMVar_hsa_circ_153410,RMVar_hsa_circ_153408 31968 RMVar_ID_31968 Human_SNP_ID_483607602 A-to-I Human chr11 + 118582284 118582284 118582284 CTGGCCTCAGCCTCCCGAGTAGTTGAGATTACAGATGTGCATCGCCATGCCTGGCTAATTTTTGT CTGGCCTCAGCCTCCCGAGTAGTTGAGATTACGGATGTGCATCGCCATGCCTGGCTAATTTTTGT A G ARCN1 Ensembl:ENSG00000095139 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs542857512 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_153409,RMVar_hsa_circ_288469,RMVar_hsa_circ_112504,RMVar_hsa_circ_317410,RMVar_hsa_circ_347413,RMVar_hsa_circ_153407,RMVar_hsa_circ_324954,RMVar_hsa_circ_309969,RMVar_hsa_circ_153411,RMVar_hsa_circ_283063,RMVar_hsa_circ_153410,RMVar_hsa_circ_153408 31969 RMVar_ID_31969 Human_SNP_ID_483609201 A-to-I Human chr11 + 118588649 118588649 118588649 GGAGGATCACTTGAGACCAGGAGTTCAAGGTTATAGTGAACTGTGATTGTGTCTCTGAATAGCCA GGAGGATCACTTGAGACCAGGAGTTCAAGGTTGTAGTGAACTGTGATTGTGTCTCTGAATAGCCA A G ARCN1 Ensembl:ENSG00000095139 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1555075811 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_153409,RMVar_hsa_circ_317410,RMVar_hsa_circ_347413,RMVar_hsa_circ_324954,RMVar_hsa_circ_309969,RMVar_hsa_circ_121647,RMVar_hsa_circ_332848,RMVar_hsa_circ_153408,RMVar_hsa_circ_378863,RMVar_hsa_circ_153413,RMVar_hsa_circ_335508,RMVar_hsa_circ_153415 31970 RMVar_ID_31970 Human_SNP_ID_483653757 A-to-I Human chr11 - 118753418 118753418 118753418 GGCGAATCACTTGAACCTGGGAGGTGGAGGTTACAGTGAGCTGAGACCGCACCACTGCACTCCAG GGCGAATCACTTGAACCTGGGAGGTGGAGGTTGCAGTGAGCTGAGACCGCACCACTGCACTCCAG T C DDX6 Ensembl:ENSG00000110367 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1159923171 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24871381 31971 RMVar_ID_31971 Human_SNP_ID_483653825 A-to-I Human chr11 - 118753566 118753565 118753567 TGGGAGGCCGAGGTGGGCGGATCACGAGGTCAAGAGATCGAGACCATCCTGGCCAACATGGTGAA TGGGAGGCCGAGGTGGGCGGATCACGAGGTC__GAGATCGAGACCATCCTGGCCAACATGGTGAA CTT C DDX6 Ensembl:ENSG00000110367 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1271504431 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_110810 31972 RMVar_ID_31972 Human_SNP_ID_483653826 A-to-I Human chr11 - 118753566 118753566 118753566 TGGGAGGCCGAGGTGGGCGGATCACGAGGTCAAGAGATCGAGACCATCCTGGCCAACATGGTGAA TGGGAGGCCGAGGTGGGCGGATCACGAGGTCAGGAGATCGAGACCATCCTGGCCAACATGGTGAA T C DDX6 Ensembl:ENSG00000110367 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1555157992 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_110810 31973 RMVar_ID_31973 Human_SNP_ID_483653917 A-to-I Human chr11 - 118753860 118753860 118753860 GAACTCCTGACCTCAAGTGATCTACCCGCCTCAGCCTCCTAAAGGGAGGCTGGGATTACAGGTGT GAACTCCTGACCTCAAGTGATCTACCCGCCTCGGCCTCCTAAAGGGAGGCTGGGATTACAGGTGT T C DDX6 Ensembl:ENSG00000110367 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs182766431 Functional Loss SNV dbSNP153 33..33 33 - - - 31974 RMVar_ID_31974 Human_SNP_ID_483653938 A-to-I Human chr11 - 118753929 118753929 118753929 ACCATGCCCAGCTAATTTTTGTATTTTTTAGTAGAGTTGGAGTTTCACCATGTTGGCCAGGTTGG ACCATGCCCAGCTAATTTTTGTATTTTTTAGTTGAGTTGGAGTTTCACCATGTTGGCCAGGTTGG T A DDX6 Ensembl:ENSG00000110367 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1187513101 Functional Loss SNV dbSNP153 33..33 33 - - - 31975 RMVar_ID_31975 Human_SNP_ID_483653977 A-to-I Human chr11 - 118754051 118754051 118754051 CTCTGTTGCCCAGGCTGGAGTACAGTGGCACAATCACGGCCCACTGCAACCTCTGCCTCCCAGGT CTCTGTTGCCCAGGCTGGAGTACAGTGGCACAGTCACGGCCCACTGCAACCTCTGCCTCCCAGGT T C DDX6 Ensembl:ENSG00000110367 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1309557377 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11539121,Human_RBP_ID_24871382 31976 RMVar_ID_31976 Human_SNP_ID_483657952 A-to-I Human chr11 - 118766806 118766804 118766806 GGGAGGCCAAGGCAGGAGGATTGCTTGAGGTCAGGGGTTTGAGACCAGCTGGGCCAACATGATGA GGGAGGCCAAGGCAGGAGGATTGCTTGAGGTC__GGGTTTGAGACCAGCTGGGCCAACATGATGA CCT C DDX6 Ensembl:ENSG00000110367 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1266892858 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_11539392 RMVar_hsa_circ_28907,RMVar_hsa_circ_338357,RMVar_hsa_circ_36289,RMVar_hsa_circ_357767,RMVar_hsa_circ_359539,RMVar_hsa_circ_287084,RMVar_hsa_circ_329828,RMVar_hsa_circ_278808,RMVar_hsa_circ_368575,RMVar_hsa_circ_323829,RMVar_hsa_circ_273168,RMVar_hsa_circ_153438 31977 RMVar_ID_31977 Human_SNP_ID_483657953 A-to-I Human chr11 - 118766806 118766806 118766806 GGGAGGCCAAGGCAGGAGGATTGCTTGAGGTCAGGGGTTTGAGACCAGCTGGGCCAACATGATGA GGGAGGCCAAGGCAGGAGGATTGCTTGAGGTCCGGGGTTTGAGACCAGCTGGGCCAACATGATGA T G DDX6 Ensembl:ENSG00000110367 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1223614343 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11539392 RMVar_hsa_circ_28907,RMVar_hsa_circ_338357,RMVar_hsa_circ_36289,RMVar_hsa_circ_357767,RMVar_hsa_circ_359539,RMVar_hsa_circ_287084,RMVar_hsa_circ_329828,RMVar_hsa_circ_278808,RMVar_hsa_circ_368575,RMVar_hsa_circ_323829,RMVar_hsa_circ_273168,RMVar_hsa_circ_153438 31978 RMVar_ID_31978 Human_SNP_ID_483657993 A-to-I Human chr11 - 118766958 118766958 118766958 TTGCTTGAACCTGGGAGGTGGAGGTTGCAGTCAGCCAAGATCATGTCACTGCACTCCAGCCTGGG TTGCTTGAACCTGGGAGGTGGAGGTTGCAGTCTGCCAAGATCATGTCACTGCACTCCAGCCTGGG T A DDX6 Ensembl:ENSG00000110367 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs535996 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22571936 RMVar_hsa_circ_28907,RMVar_hsa_circ_338357,RMVar_hsa_circ_36289,RMVar_hsa_circ_357767,RMVar_hsa_circ_359539,RMVar_hsa_circ_287084,RMVar_hsa_circ_329828,RMVar_hsa_circ_278808,RMVar_hsa_circ_368575,RMVar_hsa_circ_323829,RMVar_hsa_circ_273168,RMVar_hsa_circ_153438 31979 RMVar_ID_31979 Human_SNP_ID_483657994 A-to-I Human chr11 - 118766958 118766958 118766958 TTGCTTGAACCTGGGAGGTGGAGGTTGCAGTCAGCCAAGATCATGTCACTGCACTCCAGCCTGGG TTGCTTGAACCTGGGAGGTGGAGGTTGCAGTCGGCCAAGATCATGTCACTGCACTCCAGCCTGGG T C DDX6 Ensembl:ENSG00000110367 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs535996 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22571936 RMVar_hsa_circ_28907,RMVar_hsa_circ_338357,RMVar_hsa_circ_36289,RMVar_hsa_circ_357767,RMVar_hsa_circ_359539,RMVar_hsa_circ_287084,RMVar_hsa_circ_329828,RMVar_hsa_circ_278808,RMVar_hsa_circ_368575,RMVar_hsa_circ_323829,RMVar_hsa_circ_273168,RMVar_hsa_circ_153438 31980 RMVar_ID_31980 Human_SNP_ID_483660717 A-to-I Human chr11 - 118776711 118776711 118776711 CCCCTGCCTCAGCCTCCCGAATAGCGGGGACTACAGGCGTGCACCACAGCACCCGGCTAATTTTT CCCCTGCCTCAGCCTCCCGAATAGCGGGGACTGCAGGCGTGCACCACAGCACCCGGCTAATTTTT T C DDX6 Ensembl:ENSG00000110367 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1555163670 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_338357,RMVar_hsa_circ_36289,RMVar_hsa_circ_359539,RMVar_hsa_circ_287084,RMVar_hsa_circ_323829,RMVar_hsa_circ_273168,RMVar_hsa_circ_276233,RMVar_hsa_circ_318638 31981 RMVar_ID_31981 Human_SNP_ID_483662252 A-to-I Human chr11 - 118781852 118781852 118781852 GTGAGCTTGGCTCACTGCAGTGTCCGCCTCCCAGGTTCAAGTGATTCCCCTGCCTCAGCCTCCCG GTGAGCTTGGCTCACTGCAGTGTCCGCCTCCCGGGTTCAAGTGATTCCCCTGCCTCAGCCTCCCG T C DDX6 Ensembl:ENSG00000110367 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1332898590 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_359539,RMVar_hsa_circ_287084,RMVar_hsa_circ_323829,RMVar_hsa_circ_276233,RMVar_hsa_circ_282671,RMVar_hsa_circ_153440,RMVar_hsa_circ_337817 31982 RMVar_ID_31982 Human_SNP_ID_483662759 A-to-I Human chr11 - 118783654 118783654 118783654 GGGATTACAGGTGTCCACCATCACGTCTGGCTAATTTTTGTATTTTTAGTAGAGATGAGATTTCA GGGATTACAGGTGTCCACCATCACGTCTGGCTGATTTTTGTATTTTTAGTAGAGATGAGATTTCA T C DDX6 Ensembl:ENSG00000110367 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1334118735 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_359539,RMVar_hsa_circ_287084,RMVar_hsa_circ_323829,RMVar_hsa_circ_276233,RMVar_hsa_circ_282671,RMVar_hsa_circ_153440,RMVar_hsa_circ_337817 31983 RMVar_ID_31983 Human_SNP_ID_483662790 A-to-I Human chr11 - 118783768 118783768 118783768 CTCACTCACTCTGTTGCCCAGGCTAGAGTGCAATGGTGTGATCTCGACTCACTGCAACCTGCACC CTCACTCACTCTGTTGCCCAGGCTAGAGTGCAGTGGTGTGATCTCGACTCACTGCAACCTGCACC T C DDX6 Ensembl:ENSG00000110367 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1460789759 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_359539,RMVar_hsa_circ_287084,RMVar_hsa_circ_323829,RMVar_hsa_circ_276233,RMVar_hsa_circ_282671,RMVar_hsa_circ_153440,RMVar_hsa_circ_337817 31984 RMVar_ID_31984 Human_SNP_ID_483663061 A-to-I Human chr11 - 118784526 118784526 118784526 TGAACCCGAGAGGTGGAGGTTGCAGAGAGCCAAGATCGTGTCACTGCACTCCAGCCTGGGCAACA TGAACCCGAGAGGTGGAGGTTGCAGAGAGCCAGGATCGTGTCACTGCACTCCAGCCTGGGCAACA T C DDX6 Ensembl:ENSG00000110367 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1424322913 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_359539,RMVar_hsa_circ_287084,RMVar_hsa_circ_323829,RMVar_hsa_circ_276233,RMVar_hsa_circ_282671,RMVar_hsa_circ_153440,RMVar_hsa_circ_337817 31985 RMVar_ID_31985 Human_SNP_ID_483663923 A-to-I Human chr11 - 118787348 118787348 118787348 TCTCTGCCTCAGCCTCCCAAGTAGCTGGAATTACAGGCGCTCGCCACCACGCCTGGCTAATTTTT TCTCTGCCTCAGCCTCCCAAGTAGCTGGAATTGCAGGCGCTCGCCACCACGCCTGGCTAATTTTT T C DDX6 Ensembl:ENSG00000110367 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1257018323 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88517,RMVar_hsa_circ_104808,RMVar_hsa_circ_153442,RMVar_hsa_circ_153443 31986 RMVar_ID_31986 Human_SNP_ID_483664436 A-to-I Human chr11 - 118788806 118788806 118788806 ACCTGTAATCCCACCAAGCTACTTGGGAGGCTAAGGCATGAGGATCGCTTGAACCTGCGTGGTGG ACCTGTAATCCCACCAAGCTACTTGGGAGGCTTAGGCATGAGGATCGCTTGAACCTGCGTGGTGG T A DDX6 Ensembl:ENSG00000110367 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1388242302 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11540064 Human_miRNA_ID_2742695 RMVar_hsa_circ_88517,RMVar_hsa_circ_104808,RMVar_hsa_circ_153442,RMVar_hsa_circ_153443 31987 RMVar_ID_31987 Human_SNP_ID_483664437 A-to-I Human chr11 - 118788806 118788806 118788806 ACCTGTAATCCCACCAAGCTACTTGGGAGGCTAAGGCATGAGGATCGCTTGAACCTGCGTGGTGG ACCTGTAATCCCACCAAGCTACTTGGGAGGCTGAGGCATGAGGATCGCTTGAACCTGCGTGGTGG T C DDX6 Ensembl:ENSG00000110367 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1388242302 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11540064 Human_miRNA_ID_2742695 RMVar_hsa_circ_88517,RMVar_hsa_circ_104808,RMVar_hsa_circ_153442,RMVar_hsa_circ_153443 31988 RMVar_ID_31988 Human_SNP_ID_483664597 A-to-I Human chr11 - 118789240 118789240 118789240 AACCCCGTCTCTACTAAAAATAGAAAAAATTTAGCTGCGCGTGGTGGCAGGCGCCTGTAATCCCA AACCCCGTCTCTACTAAAAATAGAAAAAATTTGGCTGCGCGTGGTGGCAGGCGCCTGTAATCCCA T C DDX6 Ensembl:ENSG00000110367 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1372523344 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88517,RMVar_hsa_circ_104808,RMVar_hsa_circ_153442,RMVar_hsa_circ_153443 31989 RMVar_ID_31989 Human_SNP_ID_483691971 A-to-I Human chr11 - 118896458 118896458 118896458 GAGCCCTCCACCCCTGGCCCAAGACCCCCCCAAACTGTCTGACTCTGTGTTTCCTGCCCTGAGGA GAGCCCTCCACCCCTGGCCCAAGACCCCCCCAGACTGTCTGACTCTGTGTTTCCTGCCCTGAGGA T C BCL9L Ensembl:ENSG00000186174 Protein coding 3'UTR GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 29129909,30559470 RNA-Seq:(High) rs1429364683 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2252961,Human_RBP_ID_18934040,Human_RBP_ID_27409302 31990 RMVar_ID_31990 Human_SNP_ID_483696440 A-to-I Human chr11 - 118909316 118909316 118909316 CTGGAGCTTAAAGGGCCCGCAGCCTAGGCTGCAGGAATCCTTGGCTTCAAGCTACACTCCCCATC CTGGAGCTTAAAGGGCCCGCAGCCTAGGCTGCCGGAATCCTTGGCTTCAAGCTACACTCCCCATC T G BCL9L Ensembl:ENSG00000186174 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1030547687 Functional Loss SNV dbSNP153 33..33 33 - - - 31991 RMVar_ID_31991 Human_SNP_ID_483718717 A-to-I Human chr11 - 118993404 118993404 118993404 GGCCGGACACGGTGGCTCATGCCTGTAATCCCAGCACTCTGGGAGGCCGAGGCAGGCGGATCACA GGCCGGACACGGTGGCTCATGCCTGTAATCCCGGCACTCTGGGAGGCCGAGGCAGGCGGATCACA T C CCDC84-DT,CCDC84-DT:2,CCDC84-DT:3,CCDC84-DT:4 RNACentral:URS0000D5C267,RNACentral:URS0000D59A90,RNACentral:URS0000D5D3EA,RNACentral:URS0000D59875 lincRNA,lincRNA,lincRNA,lincRNA exon,intron,exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1361249416 Functional Loss SNV dbSNP153 33..33 33 - - - 31992 RMVar_ID_31992 Human_SNP_ID_483718852 A-to-I Human chr11 - 118993993 118993993 118993993 TTAAAAAAATTATATATATATATAATAGAGACAGGGTTGCGCTATGTTGCCCAGGCTGGTCTTGA TTAAAAAAATTATATATATATATAATAGAGACGGGGTTGCGCTATGTTGCCCAGGCTGGTCTTGA T C CCDC84-DT,CCDC84-DT:2,CCDC84-DT:3,CCDC84-DT:4 RNACentral:URS0000D5C267,RNACentral:URS0000D59A90,RNACentral:URS0000D5D3EA,RNACentral:URS0000D59875 lincRNA,lincRNA,lincRNA,lincRNA exon,intron,exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1403650721 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1353686 31993 RMVar_ID_31993 Human_SNP_ID_483719190 A-to-I Human chr11 - 118995406 118995406 118995406 AAACTTAGTCGGGTGTGGTGGCACGCACCTGTAGTACCAACTACTCAGGAGGCTTAGGCTGGAGA AAACTTAGTCGGGTGTGGTGGCACGCACCTGTCGTACCAACTACTCAGGAGGCTTAGGCTGGAGA T G CCDC84-DT Ensembl:ENSG00000255121 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs996656927 Functional Loss SNV dbSNP153 33..33 33 - - - 31994 RMVar_ID_31994 Human_SNP_ID_483719321 A-to-I Human chr11 - 118995880 118995880 118995880 CAAAAATTAGCCTGGTGTGGTGGCATGTGTCTAGTCCCAGCTACTCGAGAGGCTGAGGCAGGGGA CAAAAATTAGCCTGGTGTGGTGGCATGTGTCTCGTCCCAGCTACTCGAGAGGCTGAGGCAGGGGA T G CCDC84-DT Ensembl:ENSG00000255121 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1244215393 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5246203,Human_RBP_ID_22471709 31995 RMVar_ID_31995 Human_SNP_ID_483719559 A-to-I Human chr11 - 118996847 118996847 118996847 GGTGGATCACCTGAGGTCAGGAGTTGAGGACCAGCCTGGCTAACATGGTGAAACCCCGTCTCTAC GGTGGATCACCTGAGGTCAGGAGTTGAGGACCGGCCTGGCTAACATGGTGAAACCCCGTCTCTAC T C CCDC84-DT Ensembl:ENSG00000255121 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1412672581 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11540535 31996 RMVar_ID_31996 Human_SNP_ID_483720438 A-to-I Human chr11 + 118999514 118999514 118999514 GAGTTTTGCTCTTTTCGCCCAGGCTGGAGTGCAATGGCACAATCTCAGCCCACTGCAATTTCAGC GAGTTTTGCTCTTTTCGCCCAGGCTGGAGTGCGATGGCACAATCTCAGCCCACTGCAATTTCAGC A G CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1039472861 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 31997 RMVar_ID_31997 Human_SNP_ID_483720768 A-to-I Human chr11 + 119000633 119000633 119000633 CAAAAATTAGCTGGGTGTGGTGGTGGGTGCCTATAATCCCAGATACTCAGGAGGTTGAGACAGGA CAAAAATTAGCTGGGTGTGGTGGTGGGTGCCTGTAATCCCAGATACTCAGGAGGTTGAGACAGGA A G CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs371329968 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 31998 RMVar_ID_31998 Human_SNP_ID_483720796 A-to-I Human chr11 + 119000714 119000714 119000714 GCGAGGCAGAGGTTGCAGTGAGCCGAGATCGCACCACTTCACTCCAGCCTGGGCAAAAGATCGAA GCGAGGCAGAGGTTGCAGTGAGCCGAGATCGCGCCACTTCACTCCAGCCTGGGCAAAAGATCGAA A G CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1476669563 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11540622,Human_RBP_ID_22895994,Human_RBP_ID_24915139 RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 31999 RMVar_ID_31999 Human_SNP_ID_483721098 A-to-I Human chr11 + 119001998 119001998 119001998 GTAATCCCAGCACTTTGGGAGGCCGAGGTGGGAGGATCATTTGAGGTCAGGAGTTCGAGACCAGC GTAATCCCAGCACTTTGGGAGGCCGAGGTGGGCGGATCATTTGAGGTCAGGAGTTCGAGACCAGC A C CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs567276976 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 32000 RMVar_ID_32000 Human_SNP_ID_483721099 A-to-I Human chr11 + 119001998 119001998 119001998 GTAATCCCAGCACTTTGGGAGGCCGAGGTGGGAGGATCATTTGAGGTCAGGAGTTCGAGACCAGC GTAATCCCAGCACTTTGGGAGGCCGAGGTGGGTGGATCATTTGAGGTCAGGAGTTCGAGACCAGC A T CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs567276976 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 32001 RMVar_ID_32001 Human_SNP_ID_483721102 A-to-I Human chr11 + 119002014 119002014 119002014 GGGAGGCCGAGGTGGGAGGATCATTTGAGGTCAGGAGTTCGAGACCAGCTTGGTCAACATGGTGA GGGAGGCCGAGGTGGGAGGATCATTTGAGGTCGGGAGTTCGAGACCAGCTTGGTCAACATGGTGA A G CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1003599802 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 32002 RMVar_ID_32002 Human_SNP_ID_483721115 A-to-I Human chr11 + 119002062 119002062 119002062 CTTGGTCAACATGGTGAAACCCCATCCCTACTAAAAATACAAAAAATAGCTGGGCGTGTTGGTTT CTTGGTCAACATGGTGAAACCCCATCCCTACTGAAAATACAAAAAATAGCTGGGCGTGTTGGTTT A G CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1346021002 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 32003 RMVar_ID_32003 Human_SNP_ID_483721116 A-to-I Human chr11 + 119002063 119002063 119002063 TTGGTCAACATGGTGAAACCCCATCCCTACTAAAAATACAAAAAATAGCTGGGCGTGTTGGTTTG TTGGTCAACATGGTGAAACCCCATCCCTACTACAAATACAAAAAATAGCTGGGCGTGTTGGTTTG A C CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1423446727 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 32004 RMVar_ID_32004 Human_SNP_ID_483721252 A-to-I Human chr11 + 119002451 119002451 119002451 ACCTCCACCTCCCAGGTTCAAGCAGTTCTCCCATCTCAGCTTCCAGAGTAGGTGGAATTACAGGC ACCTCCACCTCCCAGGTTCAAGCAGTTCTCCCGTCTCAGCTTCCAGAGTAGGTGGAATTACAGGC A G CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1406652490 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 32005 RMVar_ID_32005 Human_SNP_ID_483721269 A-to-I Human chr11 + 119002521 119002521 119002521 CCACTACGCCTGACTAATTTTTGTATTTTAGTAAAGATGGGGTTTCACCATGTTGGCCAGGCTGG CCACTACGCCTGACTAATTTTTGTATTTTAGTGAAGATGGGGTTTCACCATGTTGGCCAGGCTGG A G CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 29129909,30559470 RNA-Seq:(High) rs1353180674 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 32006 RMVar_ID_32006 Human_SNP_ID_483721270 A-to-I Human chr11 + 119002522 119002522 119002522 CACTACGCCTGACTAATTTTTGTATTTTAGTAAAGATGGGGTTTCACCATGTTGGCCAGGCTGGT CACTACGCCTGACTAATTTTTGTATTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGT A G CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1315956278 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 32007 RMVar_ID_32007 Human_SNP_ID_483721278 A-to-I Human chr11 + 119002577 119002577 119002577 CCAGGCTGGTCTTGAACTCCTGACCTCAAGTGATCCACCTGACTCGGCTTCCCAAAGTGCTAGGA CCAGGCTGGTCTTGAACTCCTGACCTCAAGTGTTCCACCTGACTCGGCTTCCCAAAGTGCTAGGA A T CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277224947 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 32008 RMVar_ID_32008 Human_SNP_ID_483721359 A-to-I Human chr11 + 119002804 119002804 119002804 GAATCCAATAGAAATATTTCAGGTTTTTTTTCAAGATGGAGTCTCGCTCTGTTGTCCAGGCTGGA GAATCCAATAGAAATATTTCAGGTTTTTTTTCGAGATGGAGTCTCGCTCTGTTGTCCAGGCTGGA A G CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs546361091 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11540704 RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 32009 RMVar_ID_32009 Human_SNP_ID_483721545 A-to-I Human chr11 + 119003472 119003472 119003472 GTGCCATCTTGTGAAAAGGGGCTGATTTTTGTATTTTTCGTAGAGATAGGGTGTCACCATGTTGG GTGCCATCTTGTGAAAAGGGGCTGATTTTTGTCTTTTTCGTAGAGATAGGGTGTCACCATGTTGG A C CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1430758775 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6049789,Human_RBP_ID_9630898,Human_RBP_ID_11540753 RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 32010 RMVar_ID_32010 Human_SNP_ID_483721546 A-to-I Human chr11 + 119003472 119003472 119003472 GTGCCATCTTGTGAAAAGGGGCTGATTTTTGTATTTTTCGTAGAGATAGGGTGTCACCATGTTGG GTGCCATCTTGTGAAAAGGGGCTGATTTTTGTGTTTTTCGTAGAGATAGGGTGTCACCATGTTGG A G CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1430758775 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6049789,Human_RBP_ID_9630898,Human_RBP_ID_11540753 RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 32011 RMVar_ID_32011 Human_SNP_ID_483721547 A-to-I Human chr11 + 119003472 119003472 119003472 GTGCCATCTTGTGAAAAGGGGCTGATTTTTGTATTTTTCGTAGAGATAGGGTGTCACCATGTTGG GTGCCATCTTGTGAAAAGGGGCTGATTTTTGTTTTTTTCGTAGAGATAGGGTGTCACCATGTTGG A T CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1430758775 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6049789,Human_RBP_ID_9630898,Human_RBP_ID_11540753 RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 32012 RMVar_ID_32012 Human_SNP_ID_483721553 A-to-I Human chr11 - 119003486 119003486 119003486 CGAGACCAGTTTGGCCAACATGGTGACACCCTATCTCTACGAAAAATACAAAAATCAGCCCCTTT CGAGACCAGTTTGGCCAACATGGTGACACCCTGTCTCTACGAAAAATACAAAAATCAGCCCCTTT T C lnc-RPS25-3 RNACentral:URS00008BDE07 lincRNA intron GSE107867 ASD brains,cerebellum;ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1359165528 Functional Loss SNV dbSNP153 33..33 33 - - - 32013 RMVar_ID_32013 Human_SNP_ID_483721558 A-to-I Human chr11 + 119003498 119003498 119003498 TTTTGTATTTTTCGTAGAGATAGGGTGTCACCATGTTGGCCAAACTGGTCTCGAACTCCTGACCT TTTTGTATTTTTCGTAGAGATAGGGTGTCACCGTGTTGGCCAAACTGGTCTCGAACTCCTGACCT A G CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs893386224 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11540754 RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 32014 RMVar_ID_32014 Human_SNP_ID_483721623 A-to-I Human chr11 + 119003643 119003642 119003643 ATTTCTCTCTCTTTTTTTTTTTTTTTTTTGGGAGACAGAGTCTTGTTCTGTTGCCCAGGCTGGAG ATTTCTCTCTCTTTTTTTTTTTTTTTTTTGGG_GACAGAGTCTTGTTCTGTTGCCCAGGCTGGAG GA G CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1319434787 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_2253045,Human_RBP_ID_11540757 RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 32015 RMVar_ID_32015 Human_SNP_ID_483721624 A-to-I Human chr11 + 119003643 119003643 119003643 ATTTCTCTCTCTTTTTTTTTTTTTTTTTTGGGAGACAGAGTCTTGTTCTGTTGCCCAGGCTGGAG ATTTCTCTCTCTTTTTTTTTTTTTTTTTTGGGGGACAGAGTCTTGTTCTGTTGCCCAGGCTGGAG A G CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1368561995 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2253045,Human_RBP_ID_11540757 RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 32016 RMVar_ID_32016 Human_SNP_ID_483721666 A-to-I Human chr11 + 119003748 119003748 119003748 TCAAGCGATTCTCCTGCCTCAGCCTTCCGAGTAGCTGGAACTACAGGTGCATGCCACCACACCTG TCAAGCGATTCTCCTGCCTCAGCCTTCCGAGTGGCTGGAACTACAGGTGCATGCCACCACACCTG A G CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs540262313 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 32017 RMVar_ID_32017 Human_SNP_ID_483721673 A-to-I Human chr11 + 119003793 119003793 119003793 GGTGCATGCCACCACACCTGGCTAATTTTTGTAATTGTAGTAGAGATGGGGTTTTACCATATTGG GGTGCATGCCACCACACCTGGCTAATTTTTGTGATTGTAGTAGAGATGGGGTTTTACCATATTGG A G CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs577019622 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11540763 RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 32018 RMVar_ID_32018 Human_SNP_ID_483721684 A-to-I Human chr11 + 119003821 119003821 119003821 TTGTAATTGTAGTAGAGATGGGGTTTTACCATATTGGTCAGGCTGGTCTCGAACTCCCGACCTCA TTGTAATTGTAGTAGAGATGGGGTTTTACCATGTTGGTCAGGCTGGTCTCGAACTCCCGACCTCA A G CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1484560530 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 32019 RMVar_ID_32019 Human_SNP_ID_483721940 A-to-I Human chr11 + 119004877 119004877 119004877 GCCCAGGAGTTTAAGACCAGCCTGAACAACATAGTGAAACCCCATCTCTAAAAAAAAAAAATTAT GCCCAGGAGTTTAAGACCAGCCTGAACAACATGGTGAAACCCCATCTCTAAAAAAAAAAAATTAT A G CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1395059580 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 32020 RMVar_ID_32020 Human_SNP_ID_483721970 A-to-I Human chr11 + 119005017 119005017 119005017 ACAAGGTTGAGGCAGGAGTGAGCTGTGATCACACCACTGCACTCTAGCCTGGGCAACAGAGCAAA ACAAGGTTGAGGCAGGAGTGAGCTGTGATCACGCCACTGCACTCTAGCCTGGGCAACAGAGCAAA A G CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4936457 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11540803,Human_RBP_ID_17560167,Human_RBP_ID_23304733,Human_RBP_ID_24871705 RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 32021 RMVar_ID_32021 Human_SNP_ID_483722020 A-to-I Human chr11 + 119005203 119005203 119005203 AAATAAAAATTTTTGGCCGGGCACGATGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAG AAATAAAAATTTTTGGCCGGGCACGATGGCTCCTGCCTGTAATCCCAGCACTTTGGGAGGCCAAG A C CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs566228292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_110028 RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 32022 RMVar_ID_32022 Human_SNP_ID_483722021 A-to-I Human chr11 + 119005203 119005203 119005203 AAATAAAAATTTTTGGCCGGGCACGATGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAG AAATAAAAATTTTTGGCCGGGCACGATGGCTCTTGCCTGTAATCCCAGCACTTTGGGAGGCCAAG A T CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs566228292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_110028 RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 32023 RMVar_ID_32023 Human_SNP_ID_483722070 A-to-I Human chr11 + 119005421 119005421 119005421 CCAGGAGGTGGAGCTTGCAGTGAGCCGAGATCATGCCACTGCACTCCAGCCTGGCGACATAGAGT CCAGGAGGTGGAGCTTGCAGTGAGCCGAGATCGTGCCACTGCACTCCAGCCTGGCGACATAGAGT A G CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs912410937 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23153600,Human_RBP_ID_24915150 RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 32024 RMVar_ID_32024 Human_SNP_ID_483722302 A-to-I Human chr11 + 119006107 119006107 119006107 ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTGAGATGGAATCTTGCTCTGTCGCCAGGCTGGAGT ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTGTGATGGAATCTTGCTCTGTCGCCAGGCTGGAGT A T CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1442596407 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11762474,Human_RBP_ID_17560170 RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 32025 RMVar_ID_32025 Human_SNP_ID_483722324 A-to-I Human chr11 + 119006166 119006166 119006166 TGGAGTACAGTGGCGTGATCTCAGTTGACTGCAACCTCTGCCTCCCAGGTTCAAGCGATTCTCTT TGGAGTACAGTGGCGTGATCTCAGTTGACTGCCACCTCTGCCTCCCAGGTTCAAGCGATTCTCTT A C CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1336379644 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 32026 RMVar_ID_32026 Human_SNP_ID_483722438 A-to-I Human chr11 + 119006497 119006497 119006497 TGACCTCGTGATCCGCCTGCCTCGGCCTCCCAAAGTCTGGGATTACAGGCGTAAGCCACCATGCC TGACCTCGTGATCCGCCTGCCTCGGCCTCCCAGAGTCTGGGATTACAGGCGTAAGCCACCATGCC A G CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs996949091 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 32027 RMVar_ID_32027 Human_SNP_ID_483722493 A-to-I Human chr11 + 119006634 119006634 119006634 CTCGTGATCCACCCGCCTCGGCCTCCCAAAGTACTGGGATTACAGGCGTGAGCCACTGCGCCTGG CTCGTGATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCGCCTGG A G CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE47997;GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,24183664,29129909,31158229,31158229 RNA-Seq:(High) rs1013674606 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 32028 RMVar_ID_32028 Human_SNP_ID_483722652 A-to-I Human chr11 + 119007223 119007223 119007223 TTTCTTTTTTTTGGAGAGAGTCTCGCTCTGTCACCCAGGCTGGAGTGCAATGACATGATCTTGGC TTTCTTTTTTTTGGAGAGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCAATGACATGATCTTGGC A G CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1303725677 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 32029 RMVar_ID_32029 Human_SNP_ID_483722654 A-to-I Human chr11 + 119007243 119007243 119007243 TCTCGCTCTGTCACCCAGGCTGGAGTGCAATGACATGATCTTGGCTCACTGCAACCTCCGCCTCC TCTCGCTCTGTCACCCAGGCTGGAGTGCAATGGCATGATCTTGGCTCACTGCAACCTCCGCCTCC A G CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1215592864 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 32030 RMVar_ID_32030 Human_SNP_ID_483722669 A-to-I Human chr11 + 119007309 119007309 119007309 AGGTTCAAGTGATTCTCCTGCCTCAGCCTGCTAAGTAGGTGGGATTACAGGCACGTGCCACCACG AGGTTCAAGTGATTCTCCTGCCTCAGCCTGCTGAGTAGGTGGGATTACAGGCACGTGCCACCACG A G CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229,31158229,31158229,31158229,31158229 RNA-Seq:(High) rs1238722255 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 32031 RMVar_ID_32031 Human_SNP_ID_483722726 A-to-I Human chr11 + 119007533 119007533 119007533 TTATTTTGAGATGGAGTCTTGCTCTGTTGTCCAAGCTGGAGTGCCATGATACAATGACAGCTCAC TTATTTTGAGATGGAGTCTTGCTCTGTTGTCCGAGCTGGAGTGCCATGATACAATGACAGCTCAC A G CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1282853601 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11540915,Human_RBP_ID_18603868 RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 32032 RMVar_ID_32032 Human_SNP_ID_483722743 A-to-I Human chr11 + 119007602 119007602 119007602 GCCTCAACCTCCCAGGCTCAAGCAATCCTCCCACCCCAGCCTTCCAAGTATCTAGGGCTATAAGT GCCTCAACCTCCCAGGCTCAAGCAATCCTCCCGCCCCAGCCTTCCAAGTATCTAGGGCTATAAGT A G CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1206172060 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11540916 RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 32033 RMVar_ID_32033 Human_SNP_ID_483722774 A-to-I Human chr11 + 119007748 119007746 119007748 GGCTCAAGCAGTCCTTCCACTTTGGCATCCCAAAGTGTTGAGATTACAGGCATGAGCCACTGTGC GGCTCAAGCAGTCCTTCCACTTTGGCATCCC__AGTGTTGAGATTACAGGCATGAGCCACTGTGC CAA C CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;ASD brains,temporal_cortex;Bronchiolar epithelium,BEP2D cell line - 29129909,30559470,31158229 RNA-Seq:(High) rs1239624030 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 32034 RMVar_ID_32034 Human_SNP_ID_483722774 A-to-I Human chr11 + 119007747 119007746 119007748 GGGCTCAAGCAGTCCTTCCACTTTGGCATCCCAAAGTGTTGAGATTACAGGCATGAGCCACTGTG GGGCTCAAGCAGTCCTTCCACTTTGGCATCCC__AGTGTTGAGATTACAGGCATGAGCCACTGTG CAA C CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1239624030 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 32035 RMVar_ID_32035 Human_SNP_ID_483722775 A-to-I Human chr11 + 119007748 119007748 119007748 GGCTCAAGCAGTCCTTCCACTTTGGCATCCCAAAGTGTTGAGATTACAGGCATGAGCCACTGTGC GGCTCAAGCAGTCCTTCCACTTTGGCATCCCAGAGTGTTGAGATTACAGGCATGAGCCACTGTGC A G CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;ASD brains,temporal_cortex;Bronchiolar epithelium,BEP2D cell line - 29129909,30559470,31158229 RNA-Seq:(High) rs1203335571 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 32036 RMVar_ID_32036 Human_SNP_ID_483722776 A-to-I Human chr11 + 119007748 119007748 119007748 GGCTCAAGCAGTCCTTCCACTTTGGCATCCCAAAGTGTTGAGATTACAGGCATGAGCCACTGTGC GGCTCAAGCAGTCCTTCCACTTTGGCATCCCATAGTGTTGAGATTACAGGCATGAGCCACTGTGC A T CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;ASD brains,temporal_cortex;Bronchiolar epithelium,BEP2D cell line - 29129909,30559470,31158229 RNA-Seq:(High) rs1203335571 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 32037 RMVar_ID_32037 Human_SNP_ID_483723151 A-to-I Human chr11 + 119009228 119009228 119009228 TCGGCTCACTGCAACCTCCACCTCCGAGGTTCAAGCAATTCTCGTCTCAGCCTCCCAAGTAGCTG TCGGCTCACTGCAACCTCCACCTCCGAGGTTCGAGCAATTCTCGTCTCAGCCTCCCAAGTAGCTG A G CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE47997;GSE100210;GSE107867 K562 cells&HepG2 cells;HepG2 cell line;ASD brains,cerebellum - 23474544,29129909,30559470 RNA-Seq:(High) rs958579381 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 32038 RMVar_ID_32038 Human_SNP_ID_483723163 A-to-I Human chr11 + 119009256 119009256 119009256 GTTCAAGCAATTCTCGTCTCAGCCTCCCAAGTAGCTGGGATTACAGGCACCTGCCACCACATCTG GTTCAAGCAATTCTCGTCTCAGCCTCCCAAGTTGCTGGGATTACAGGCACCTGCCACCACATCTG A T CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs570991440 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 32039 RMVar_ID_32039 Human_SNP_ID_483723165 A-to-I Human chr11 + 119009266 119009266 119009266 TTCTCGTCTCAGCCTCCCAAGTAGCTGGGATTACAGGCACCTGCCACCACATCTGGCTAATTTTT TTCTCGTCTCAGCCTCCCAAGTAGCTGGGATTTCAGGCACCTGCCACCACATCTGGCTAATTTTT A T CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1189148966 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 32040 RMVar_ID_32040 Human_SNP_ID_483723300 A-to-I Human chr11 + 119009868 119009868 119009868 GAGGTGACAGTACAAATTACTGATTTAAGGCCAGGCATAGTGGCTGATGCCTGTAATCCCAGTTC GAGGTGACAGTACAAATTACTGATTTAAGGCCGGGCATAGTGGCTGATGCCTGTAATCCCAGTTC A G CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE38233;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;Bronchiolar epithelium,BERP35T4 cell line - 24183664,31158229 RNA-Seq:(High) rs576322815 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11541001,Human_RBP_ID_24871737 RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 32041 RMVar_ID_32041 Human_SNP_ID_483723305 A-to-I Human chr11 + 119009890 119009890 119009890 ATTTAAGGCCAGGCATAGTGGCTGATGCCTGTAATCCCAGTTCTTTGGGAGGCCAAGGCAGGAGA ATTTAAGGCCAGGCATAGTGGCTGATGCCTGTGATCCCAGTTCTTTGGGAGGCCAAGGCAGGAGA A G CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE38233;GSE100210;GSE100210;GSE99789;GSE107867;GSE107867;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;HepG2 cell line;esophageal squamous carcinoma cells,EC109;ASD brains,cerebellum;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,29129909,29796672,30559470,30559470,30559470,31158229,31158229,32596459 RNA-Seq:(High) rs895693219 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 32042 RMVar_ID_32042 Human_SNP_ID_483723312 A-to-I Human chr11 + 119009912 119009912 119009912 TGATGCCTGTAATCCCAGTTCTTTGGGAGGCCAAGGCAGGAGAATTGCTTGAGCCCAGGAGTTCG TGATGCCTGTAATCCCAGTTCTTTGGGAGGCCGAGGCAGGAGAATTGCTTGAGCCCAGGAGTTCG A G CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE99789;GSE123020:GSM3490832,GSM3490833,GSM3490834;GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,KYSE180 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29796672,32596459,32596459 RNA-Seq:(High) rs1022859962 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 32043 RMVar_ID_32043 Human_SNP_ID_483723336 A-to-I Human chr11 + 119010003 119010003 119010003 CCCTGTTTCTACAAAAAACACAAAAATTAGCCAGGCATAGTGGTGCTGTCCTGTAGTCCTACCTA CCCTGTTTCTACAAAAAACACAAAAATTAGCCTGGCATAGTGGTGCTGTCCTGTAGTCCTACCTA A T CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs1347732379 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11541014 RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 32044 RMVar_ID_32044 Human_SNP_ID_483723341 A-to-I Human chr11 + 119010025 119010025 119010025 AAAATTAGCCAGGCATAGTGGTGCTGTCCTGTAGTCCTACCTACTCAGGAAGCTAAGGCAGGAGG AAAATTAGCCAGGCATAGTGGTGCTGTCCTGTGGTCCTACCTACTCAGGAAGCTAAGGCAGGAGG A G CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE47997;GSE38233;GSE100210;GSE99789;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BERP35T4 cell line - 23474544,24183664,29129909,29796672,31158229 RNA-Seq:(High) rs987705755 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11541015 RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 32045 RMVar_ID_32045 Human_SNP_ID_483723351 A-to-I Human chr11 + 119010086 119010086 119010086 GAGGATCTCTTGAGCCTGGGAGCCTCTTGAGCAGAGGTTGCAGCGAGCTGAGGTTGTGCCACTGC GAGGATCTCTTGAGCCTGGGAGCCTCTTGAGCGGAGGTTGCAGCGAGCTGAGGTTGTGCCACTGC A G CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1357936811 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11541016,Human_RBP_ID_17560171 RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 32046 RMVar_ID_32046 Human_SNP_ID_483724780 A-to-I Human chr11 + 119014471 119014471 119014471 GGGCATCGCAGCGCACGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGAATTGTTTGAACCG GGGCATCGCAGCGCACGCCTGTAATCCCAGCTCCTTGGGAGGCTGAGGCAGAATTGTTTGAACCG A C CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs889046609 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 32047 RMVar_ID_32047 Human_SNP_ID_483724781 A-to-I Human chr11 + 119014471 119014471 119014471 GGGCATCGCAGCGCACGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGAATTGTTTGAACCG GGGCATCGCAGCGCACGCCTGTAATCCCAGCTGCTTGGGAGGCTGAGGCAGAATTGTTTGAACCG A G CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs889046609 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 32048 RMVar_ID_32048 Human_SNP_ID_483725591 A-to-I Human chr11 - 119016169 119016169 119016169 TGGTCCTCACCTCAGCTTCCCAAGTAGCTGGAATTACAAGCATGTGCCACCATGCCCAGCTAATT TGGTCCTCACCTCAGCTTCCCAAGTAGCTGGACTTACAAGCATGTGCCACCATGCCCAGCTAATT T G RPS25 Ensembl:ENSG00000118181 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs545923391 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124755,RMVar_hsa_circ_153450,RMVar_hsa_circ_99886,RMVar_hsa_circ_153449 32049 RMVar_ID_32049 Human_SNP_ID_483725594 A-to-I Human chr11 - 119016180 119016180 119016180 CTGGGTTCAGGTGGTCCTCACCTCAGCTTCCCAAGTAGCTGGAATTACAAGCATGTGCCACCATG CTGGGTTCAGGTGGTCCTCACCTCAGCTTCCCGAGTAGCTGGAATTACAAGCATGTGCCACCATG T C RPS25 Ensembl:ENSG00000118181 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1212409884 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22158899 RMVar_hsa_circ_124755,RMVar_hsa_circ_153450,RMVar_hsa_circ_99886,RMVar_hsa_circ_153449 32050 RMVar_ID_32050 Human_SNP_ID_483725614 A-to-I Human chr11 - 119016223 119016223 119016223 GGAGTGCGGAGGGGCAGTCTTGGCTCAATGCAACCACCAATTCCTGGGTTCAGGTGGTCCTCACC GGAGTGCGGAGGGGCAGTCTTGGCTCAATGCAGCCACCAATTCCTGGGTTCAGGTGGTCCTCACC T C RPS25 Ensembl:ENSG00000118181 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs376194661 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124755,RMVar_hsa_circ_153450,RMVar_hsa_circ_99886,RMVar_hsa_circ_153449 32051 RMVar_ID_32051 Human_SNP_ID_483725828 A-to-I Human chr11 - 119016727 119016727 119016727 ACTCAGGATGCTGAGGCATGAGGATCCCTTGAACCCAGGAGATGGAGGTGGCAGTGAGCCGAGAT ACTCAGGATGCTGAGGCATGAGGATCCCTTGAGCCCAGGAGATGGAGGTGGCAGTGAGCCGAGAT T C RPS25 Ensembl:ENSG00000118181 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1181706128 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11541178 RMVar_hsa_circ_124755,RMVar_hsa_circ_153450,RMVar_hsa_circ_99886,RMVar_hsa_circ_153449 32052 RMVar_ID_32052 Human_SNP_ID_483725840 A-to-I Human chr11 - 119016755 119016755 119016755 GTGGGGGCACACGTCTGTAATCCCAGCTACTCAGGATGCTGAGGCATGAGGATCCCTTGAACCCA GTGGGGGCACACGTCTGTAATCCCAGCTACTCGGGATGCTGAGGCATGAGGATCCCTTGAACCCA T C RPS25 Ensembl:ENSG00000118181 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1327875644 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8345441,Human_RBP_ID_11541182 RMVar_hsa_circ_124755,RMVar_hsa_circ_153450,RMVar_hsa_circ_99886,RMVar_hsa_circ_153449 32053 RMVar_ID_32053 Human_SNP_ID_483728006 A-to-I Human chr11 + 119022381 119022381 119022381 GGAAGACGGAGAGGGTAGGATCACTTCAGCCCAGGAGTTTGAGATCAGCCTGGACAACATAGAAC GGAAGACGGAGAGGGTAGGATCACTTCAGCCCGGGAGTTTGAGATCAGCCTGGACAACATAGAAC A G TRAPPC4 Ensembl:ENSG00000196655 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs953156747 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89982,RMVar_hsa_circ_77421,RMVar_hsa_circ_153453,RMVar_hsa_circ_153454 32054 RMVar_ID_32054 Human_SNP_ID_483728033 A-to-I Human chr11 + 119022507 119022507 119022507 CTATTAAGGAAGCTGAGGCGGGAGGATTGCTTAAACCTGGAAGGTCAAGGCAGCAGTGAACCATG CTATTAAGGAAGCTGAGGCGGGAGGATTGCTTCAACCTGGAAGGTCAAGGCAGCAGTGAACCATG A C TRAPPC4 Ensembl:ENSG00000196655 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1411271458 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89982,RMVar_hsa_circ_77421,RMVar_hsa_circ_153453,RMVar_hsa_circ_153454 32055 RMVar_ID_32055 Human_SNP_ID_483752985 A-to-I Human chr11 - 119102237 119102237 119102237 GAGCCGGAGGCATCCCAGATTAAGGGAGAGGTACGGGCCCTTTAAGCTTGACCTATGGAGGCGGA GAGCCGGAGGCATCCCAGATTAAGGGAGAGGTGCGGGCCCTTTAAGCTTGACCTATGGAGGCGGA T C DPAGT1 Ensembl:ENSG00000172269 Protein coding 5'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1383414656 Functional Loss SNV dbSNP153 33..33 33 - - - 32056 RMVar_ID_32056 Human_SNP_ID_483758250 A-to-I Human chr11 + 119123029 119123029 119123029 CTTATAGTCCCAGCTATAATACTTCGGAGGCTAAGTCACGAGAATCGCTTGAACCTGGGAGGCGG CTTATAGTCCCAGCTATAATACTTCGGAGGCTGAGTCACGAGAATCGCTTGAACCTGGGAGGCGG A G HINFP Ensembl:ENSG00000172273 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs997669411 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_153494,RMVar_hsa_circ_82795,RMVar_hsa_circ_114694,RMVar_hsa_circ_153495 32057 RMVar_ID_32057 Human_SNP_ID_483758267 A-to-I Human chr11 + 119123069 119123069 119123069 AGAATCGCTTGAACCTGGGAGGCGGAGGTTGCAGTGAGCCCAGATCACAGCACTGCACTCCAGCC AGAATCGCTTGAACCTGGGAGGCGGAGGTTGCGGTGAGCCCAGATCACAGCACTGCACTCCAGCC A G HINFP Ensembl:ENSG00000172273 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs889644832 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_153494,RMVar_hsa_circ_82795,RMVar_hsa_circ_114694,RMVar_hsa_circ_153495 32058 RMVar_ID_32058 Human_SNP_ID_483758533 A-to-I Human chr11 + 119123768 119123768 119123768 TTGAATCTTGCTCTGTCACTAGGCTGGAGTGCAATGGTGCGATCTCGGCTCACTGCAACCTCTGT TTGAATCTTGCTCTGTCACTAGGCTGGAGTGCGATGGTGCGATCTCGGCTCACTGCAACCTCTGT A G HINFP Ensembl:ENSG00000172273 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1217420002 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_153494,RMVar_hsa_circ_82795,RMVar_hsa_circ_114694,RMVar_hsa_circ_153495,RMVar_hsa_circ_324816 32059 RMVar_ID_32059 Human_SNP_ID_483758800 A-to-I Human chr11 + 119124775 119124775 119124775 GCGGGTGGATCACCTGAGGACAGGAGTTCGAGACCAGCCTGGCCATCATGGTGAAACTCTGTCTC GCGGGTGGATCACCTGAGGACAGGAGTTCGAGTCCAGCCTGGCCATCATGGTGAAACTCTGTCTC A T HINFP Ensembl:ENSG00000172273 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1478195380 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_153494,RMVar_hsa_circ_82795,RMVar_hsa_circ_114694,RMVar_hsa_circ_153495,RMVar_hsa_circ_324816 32060 RMVar_ID_32060 Human_SNP_ID_483758810 A-to-I Human chr11 + 119124809 119124809 119124809 CAGCCTGGCCATCATGGTGAAACTCTGTCTCTAGCAAAAATACAAAAATTAGCCAGGCGTGGTGA CAGCCTGGCCATCATGGTGAAACTCTGTCTCTGGCAAAAATACAAAAATTAGCCAGGCGTGGTGA A G HINFP Ensembl:ENSG00000172273 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1318035690 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_153494,RMVar_hsa_circ_82795,RMVar_hsa_circ_114694,RMVar_hsa_circ_153495,RMVar_hsa_circ_324816 32061 RMVar_ID_32061 Human_SNP_ID_483758985 A-to-I Human chr11 + 119125378 119125378 119125378 TTCAGTTTCATGTTTATCTTTCTTCAATAAATATTTATTACAGACTGGGTGCAGTGGCTCATGCC TTCAGTTTCATGTTTATCTTTCTTCAATAAATGTTTATTACAGACTGGGTGCAGTGGCTCATGCC A G HINFP Ensembl:ENSG00000172273 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1417381203 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11541982 RMVar_hsa_circ_153494,RMVar_hsa_circ_82795,RMVar_hsa_circ_114694,RMVar_hsa_circ_153495,RMVar_hsa_circ_324816 32062 RMVar_ID_32062 Human_SNP_ID_483759033 A-to-I Human chr11 + 119125566 119125566 119125566 AGATGTGGTGGCGCATGCCTGTGGTCCCAGTTACTTGGGAGGCTGAGGTAGGAGGATCTCCTGAG AGATGTGGTGGCGCATGCCTGTGGTCCCAGTTGCTTGGGAGGCTGAGGTAGGAGGATCTCCTGAG A G HINFP Ensembl:ENSG00000172273 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1384440058 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_153494,RMVar_hsa_circ_82795,RMVar_hsa_circ_114694,RMVar_hsa_circ_153495,RMVar_hsa_circ_324816 32063 RMVar_ID_32063 Human_SNP_ID_483759056 A-to-I Human chr11 + 119125660 119125659 119125661 TGATTGTGCCACTGTACTCCAGCCTGGGTGACAGGGTGAGACTCTGTCTCAAGAAAAAAAATATT TGATTGTGCCACTGTACTCCAGCCTGGGTGAC__GGTGAGACTCTGTCTCAAGAAAAAAAATATT CAG C HINFP Ensembl:ENSG00000172273 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1225643266 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_2253181 RMVar_hsa_circ_153494,RMVar_hsa_circ_82795,RMVar_hsa_circ_114694,RMVar_hsa_circ_153495,RMVar_hsa_circ_324816 32064 RMVar_ID_32064 Human_SNP_ID_483760653 A-to-I Human chr11 + 119131222 119131222 119131222 GCAATCCTCCCACCTCAGCCTCCCAAGTAGCTAGGACTACAGGCATGTACCACCATGCCCTGCTA GCAATCCTCCCACCTCAGCCTCCCAAGTAGCTGGGACTACAGGCATGTACCACCATGCCCTGCTA A G HINFP Ensembl:ENSG00000172273 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1246974972 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78722,RMVar_hsa_circ_153494,RMVar_hsa_circ_82795,RMVar_hsa_circ_114694,RMVar_hsa_circ_153495,RMVar_hsa_circ_318344,RMVar_hsa_circ_123930,RMVar_hsa_circ_153498,RMVar_hsa_circ_153499,RMVar_hsa_circ_153497,RMVar_hsa_circ_309930 32065 RMVar_ID_32065 Human_SNP_ID_483783219 A-to-I Human chr11 + 119213003 119213002 119213004 TCAAAAAAAAAGAAAAAAAAAAAAATAGAGACAGAATCTTGACAGTGTTGCCCAGGCTGGTCTCA TCAAAAAAAAAGAAAAAAAAAAAAATAGAGAC__AATCTTGACAGTGTTGCCCAGGCTGGTCTCA CAG C CBL Ensembl:ENSG00000110395 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991519515 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_81665,RMVar_hsa_circ_153511 32066 RMVar_ID_32066 Human_SNP_ID_483804608 A-to-I Human chr11 + 119293382 119293382 119293382 CACCCACCTTTGCCTCCCAAAGGGCTGGGATTACAGACGTGAGCCATCGTGCCCATCCCATCTTC CACCCACCTTTGCCTCCCAAAGGGCTGGGATTGCAGACGTGAGCCATCGTGCCCATCCCATCTTC A G CBL Ensembl:ENSG00000110395 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1468331674 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_367968,RMVar_hsa_circ_153520,RMVar_hsa_circ_126831,RMVar_hsa_circ_82941,RMVar_hsa_circ_153521,RMVar_hsa_circ_306433,RMVar_hsa_circ_357301,RMVar_hsa_circ_153532,RMVar_hsa_circ_80991,RMVar_hsa_circ_349503,RMVar_hsa_circ_41211,RMVar_hsa_circ_153534,RMVar_hsa_circ_311643 32067 RMVar_ID_32067 Human_SNP_ID_483936412 A-to-I Human chr11 - 119821986 119821986 119821986 TACCTTGAGCAAAGAGATCCGTCCAGTCTGCCACAAGTTCATGCAAGATCCAGTGGAGATCTTCA TACCTTGAGCAAAGAGATCCGTCCAGTCTGCCGCAAGTTCATGCAAGATCCAGTGGAGATCTTCA T C AP001994.1 Ensembl:ENSG00000254406 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1212218296 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17350743,Human_RBP_ID_26401647 32068 RMVar_ID_32068 Human_SNP_ID_279473725 A-to-I Human chr6 - 62239823 62239823 62239823 AAATTGGTCGGGCATGGTGGTGGGCACCTGTAATCCCAGCTACTCAGGAGGCTGAGACAAGAGAG AAATTGGTCGGGCATGGTGGTGGGCACCTGTAGTCCCAGCTACTCAGGAGGCTGAGACAAGAGAG T C KHDRBS2 Ensembl:ENSG00000112232 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1276701693 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_239241,RMVar_hsa_circ_239242 32069 RMVar_ID_32069 Human_SNP_ID_279785298 A-to-I Human chr6 - 63277950 63277950 63277950 CCTGCCTCAGCCTCCCAAGTAGCTGGGATCCCAGGTGCCTGCTACCATGCCTGGCCTTTTAGTAG CCTGCCTCAGCCTCCCAAGTAGCTGGGATCCCGGGTGCCTGCTACCATGCCTGGCCTTTTAGTAG T C LGSN Ensembl:ENSG00000146166 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1007405281 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7621536 32070 RMVar_ID_32070 Human_SNP_ID_279802597 A-to-I Human chr6 - 63346181 63346181 63346181 TTAAAACAAGAGACACTCCTATCACCCAGGAAATTTCAAGGGATTGGGAGCTCTGTGTCAAAGAC TTAAAACAAGAGACACTCCTATCACCCAGGAAGTTTCAAGGGATTGGGAGCTCTGTGTCAAAGAC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs114073890 Functional Loss SNV dbSNP153 33..33 33 - - - 32071 RMVar_ID_32071 Human_SNP_ID_279802601 A-to-I Human chr6 - 63346193 63346193 63346193 AGAGTTGCCTCATTAAAACAAGAGACACTCCTATCACCCAGGAAATTTCAAGGGATTGGGAGCTC AGAGTTGCCTCATTAAAACAAGAGACACTCCTGTCACCCAGGAAATTTCAAGGGATTGGGAGCTC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs115207674 Functional Loss SNV dbSNP153 33..33 33 - - - 32072 RMVar_ID_32072 Human_SNP_ID_279802779 A-to-I Human chr6 - 63347019 63347019 63347019 CTCTTGTTCTAATGAGGCAACTTTTGGTGGGCATCTGAATGGAGGCTGGTAACCAGAAAGACTAA CTCTTGTTCTAATGAGGCAACTTTTGGTGGGCGTCTGAATGGAGGCTGGTAACCAGAAAGACTAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs551238018 Functional Loss SNV dbSNP153 33..33 33 - - - 32073 RMVar_ID_32073 Human_SNP_ID_279844458 A-to-I Human chr6 - 63505395 63505395 63505395 TTTTGTATTTTTAGTAGAGACGGGGTTTCACTATGTTGACCAGGCTGGCCTTGAACTCCTGACCT TTTTGTATTTTTAGTAGAGACGGGGTTTCACTGTGTTGACCAGGCTGGCCTTGAACTCCTGACCT T C RF00017-1190 RNACentral:URS000092EF5C SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs950020145 Functional Loss SNV dbSNP153 33..33 33 - - - 32074 RMVar_ID_32074 Human_SNP_ID_279850588 A-to-I Human chr6 + 63528467 63528467 63528467 TTTTTTAAGGCCGGGTACAGTGGTTCATGCCTATAATCCTAATACTTTGGGAGGCCAAGGTGGAC TTTTTTAAGGCCGGGTACAGTGGTTCATGCCTGTAATCCTAATACTTTGGGAGGCCAAGGTGGAC A G PTP4A1 Ensembl:ENSG00000112245 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1290776922 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_792433,Human_RBP_ID_22482646 RMVar_hsa_circ_107737,RMVar_hsa_circ_239243,RMVar_hsa_circ_97967,RMVar_hsa_circ_239245 32075 RMVar_ID_32075 Human_SNP_ID_279852466 A-to-I Human chr6 + 63535329 63535329 63535329 TCTACTAAAAATACAAAAAATAAGCCAGGCATAGTGGCATGCTTGTAATCCCAGCTACTCAACTT TCTACTAAAAATACAAAAAATAAGCCAGGCATGGTGGCATGCTTGTAATCCCAGCTACTCAACTT A G PTP4A1 Ensembl:ENSG00000112245 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1047789890 Functional Loss SNV dbSNP153 33..33 33 - - - 32076 RMVar_ID_32076 Human_SNP_ID_279853325 A-to-I Human chr6 + 63539073 63539073 63539073 CGCCACCATACCCGGCTAATTTGTGTTTTTTTAGTAGAGTAGAGGTTTCACCATGTTGGCCCATG CGCCACCATACCCGGCTAATTTGTGTTTTTTTTGTAGAGTAGAGGTTTCACCATGTTGGCCCATG A T PTP4A1 Ensembl:ENSG00000112245 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1465158589 Functional Loss SNV dbSNP153 33..33 33 - - - 32077 RMVar_ID_32077 Human_SNP_ID_279853346 A-to-I Human chr6 + 63539141 63539141 63539141 ATCTTGAACTCCTGACCTAAGGTGGTCCACCCACCTTGGCTTCCCAAAGTACTGGGATTACAGTC ATCTTGAACTCCTGACCTAAGGTGGTCCACCCGCCTTGGCTTCCCAAAGTACTGGGATTACAGTC A G PTP4A1 Ensembl:ENSG00000112245 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1002805003 Functional Loss SNV dbSNP153 33..33 33 - - - 32078 RMVar_ID_32078 Human_SNP_ID_279858522 A-to-I Human chr6 - 63559804 63559804 63559804 TGGGCAAACCTGCCTCAGACTCCCAAAGTGCTAGTATTATATGCATGAACGACCATGCCTGGCTG TGGGCAAACCTGCCTCAGACTCCCAAAGTGCTGGTATTATATGCATGAACGACCATGCCTGGCTG T C RF00017-1190 RNACentral:URS000092EF5C SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1189576464 Functional Loss SNV dbSNP153 33..33 33 - - - 32079 RMVar_ID_32079 Human_SNP_ID_279864297 A-to-I Human chr6 + 63582785 63582785 63582785 ACTCTGGAAGTAGGTGCCATTGGTCATTCTGCAGTGCACTGCAACCATTGTTTCCCCTAGTGCCC ACTCTGGAAGTAGGTGCCATTGGTCATTCTGCGGTGCACTGCAACCATTGTTTCCCCTAGTGCCC A G PTP4A1,AL135905.2 Ensembl:ENSG00000112245,Ensembl:ENSG00000285976 Protein coding,Protein coding 3'UTR,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs527559577 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_667018,Human_RBP_ID_1048335,Human_RBP_ID_15863761,Human_RBP_ID_17307740,Human_RBP_ID_17536735,Human_RBP_ID_18372746,Human_RBP_ID_26828612 Human_miRNA_ID_622086 32080 RMVar_ID_32080 Human_SNP_ID_279891099 A-to-I Human chr6 + 63688435 63688435 63688435 TTGGCTGACTGAAACCTCCACCTCCTGAGTTCAAGTGATTCTCCTGCCTCGGCCTCCCAAGTAGC TTGGCTGACTGAAACCTCCACCTCCTGAGTTCGAGTGATTCTCCTGCCTCGGCCTCCCAAGTAGC A G PHF3 Ensembl:ENSG00000118482 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1236862355 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17576882 RMVar_hsa_circ_6977,RMVar_hsa_circ_2534,RMVar_hsa_circ_362952,RMVar_hsa_circ_363564,RMVar_hsa_circ_354004,RMVar_hsa_circ_44387,RMVar_hsa_circ_34771,RMVar_hsa_circ_66274,RMVar_hsa_circ_363552,RMVar_hsa_circ_35129,RMVar_hsa_circ_359109,RMVar_hsa_circ_304675,RMVar_hsa_circ_56677,RMVar_hsa_circ_72874,RMVar_hsa_circ_23531,RMVar_hsa_circ_28503,RMVar_hsa_circ_74808 32081 RMVar_ID_32081 Human_SNP_ID_279902882 A-to-I Human chr6 + 63734022 63734017 63734023 TGGAGGCAATTGTCCTAAGCAAATTAACACAGAAACAGAAAACCAAATACTGTGTGTTCTCATAA TGGAGGCAATTGTCCTAAGCAAATTAAC______ACAGAAAACCAAATACTGTGTGTTCTCATAA CACAGAA C PHF3 Ensembl:ENSG00000118482 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1230492705 Functional Loss DEL dbSNP153 29..34 33 - - - 32082 RMVar_ID_32082 Human_SNP_ID_279902882 A-to-I Human chr6 + 63734023 63734017 63734023 GGAGGCAATTGTCCTAAGCAAATTAACACAGAAACAGAAAACCAAATACTGTGTGTTCTCATAAG GGAGGCAATTGTCCTAAGCAAATTAAC______ACAGAAAACCAAATACTGTGTGTTCTCATAAG CACAGAA C PHF3 Ensembl:ENSG00000118482 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1230492705 Functional Loss DEL dbSNP153 28..33 33 - - - 32083 RMVar_ID_32083 Human_SNP_ID_279902883 A-to-I Human chr6 + 63734018 63734018 63734018 CAGGTGGAGGCAATTGTCCTAAGCAAATTAACACAGAAACAGAAAACCAAATACTGTGTGTTCTC CAGGTGGAGGCAATTGTCCTAAGCAAATTAACGCAGAAACAGAAAACCAAATACTGTGTGTTCTC A G PHF3 Ensembl:ENSG00000118482 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs915411646 Functional Loss SNV dbSNP153 33..33 33 - - - 32084 RMVar_ID_32084 Human_SNP_ID_279902885 A-to-I Human chr6 + 63734022 63734022 63734022 TGGAGGCAATTGTCCTAAGCAAATTAACACAGAAACAGAAAACCAAATACTGTGTGTTCTCATAA TGGAGGCAATTGTCCTAAGCAAATTAACACAGGAACAGAAAACCAAATACTGTGTGTTCTCATAA A G PHF3 Ensembl:ENSG00000118482 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1291348568 Functional Loss SNV dbSNP153 33..33 33 - - - 32085 RMVar_ID_32085 Human_SNP_ID_279902887 A-to-I Human chr6 + 63734026 63734026 63734026 GGCAATTGTCCTAAGCAAATTAACACAGAAACAGAAAACCAAATACTGTGTGTTCTCATAAGTGG GGCAATTGTCCTAAGCAAATTAACACAGAAACCGAAAACCAAATACTGTGTGTTCTCATAAGTGG A C PHF3 Ensembl:ENSG00000118482 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270157096 Functional Loss SNV dbSNP153 33..33 33 - - - 32086 RMVar_ID_32086 Human_SNP_ID_279902888 A-to-I Human chr6 + 63734026 63734026 63734026 GGCAATTGTCCTAAGCAAATTAACACAGAAACAGAAAACCAAATACTGTGTGTTCTCATAAGTGG GGCAATTGTCCTAAGCAAATTAACACAGAAACGGAAAACCAAATACTGTGTGTTCTCATAAGTGG A G PHF3 Ensembl:ENSG00000118482 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270157096 Functional Loss SNV dbSNP153 33..33 33 - - - 32087 RMVar_ID_32087 Human_SNP_ID_279902905 A-to-I Human chr6 + 63734065 63734065 63734065 CAAATACTGTGTGTTCTCATAAGTGGGAGCTAAACATTGGATACACATGGACATAAAGATGGGAA CAAATACTGTGTGTTCTCATAAGTGGGAGCTAGACATTGGATACACATGGACATAAAGATGGGAA A G PHF3 Ensembl:ENSG00000118482 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1165243446 Functional Loss SNV dbSNP153 33..33 33 - - - 32088 RMVar_ID_32088 Human_SNP_ID_281227489 A-to-I Human chr6 + 68643871 68643871 68643871 AGAGAATTGCTTGAACCCTGGAGGCAGAGGTTACAGTGAGCCGAGATCGCACCACTGCACTCCAG AGAGAATTGCTTGAACCCTGGAGGCAGAGGTTGCAGTGAGCCGAGATCGCACCACTGCACTCCAG A G ADGRB3 Ensembl:ENSG00000135298 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1561981003 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91695,RMVar_hsa_circ_239265 32089 RMVar_ID_32089 Human_SNP_ID_281234500 A-to-I Human chr6 + 68673109 68673109 68673109 TGCATCTGTCTGTGTGTATGTTTGTGTATGTTAGGTGCAATAATAATTAAATGACAAGAACGATT TGCATCTGTCTGTGTGTATGTTTGTGTATGTTGGGTGCAATAATAATTAAATGACAAGAACGATT A G ADGRB3 Ensembl:ENSG00000135298 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1469862302 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24169435 RMVar_hsa_circ_91695,RMVar_hsa_circ_239265 32090 RMVar_ID_32090 Human_SNP_ID_281235210 A-to-I Human chr6 + 68676271 68676271 68676271 AATATTAGCTGGGCGTGGTGGCGCGTGCCTGTAATCCCGCTACTCAGGAGGCTAAGGCGAGATAA AATATTAGCTGGGCGTGGTGGCGCGTGCCTGTGATCCCGCTACTCAGGAGGCTAAGGCGAGATAA A G ADGRB3 Ensembl:ENSG00000135298 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1402643153 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91695,RMVar_hsa_circ_239265 32091 RMVar_ID_32091 Human_SNP_ID_281235646 A-to-I Human chr6 + 68677667 68677667 68677667 TGCCTCCTGAGTAGCTGGGACGACAGACGCGCACCAACACACTGGGCGAATTTTTGTAGTTTTTG TGCCTCCTGAGTAGCTGGGACGACAGACGCGCGCCAACACACTGGGCGAATTTTTGTAGTTTTTG A G ADGRB3 Ensembl:ENSG00000135298 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs757223475 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91695,RMVar_hsa_circ_239265 32092 RMVar_ID_32092 Human_SNP_ID_281236531 A-to-I Human chr6 + 68681421 68681421 68681421 CCCACCTCAGCCCCCCATGCAGCTAGGACTACAAGCATGTGCCACCACATCTGGCCAATCTTTCT CCCACCTCAGCCCCCCATGCAGCTAGGACTACGAGCATGTGCCACCACATCTGGCCAATCTTTCT A G ADGRB3 Ensembl:ENSG00000135298 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs555612373 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91695,RMVar_hsa_circ_239265 32093 RMVar_ID_32093 Human_SNP_ID_281237487 A-to-I Human chr6 + 68685762 68685762 68685762 AAGAAAAAAAAAAATTAGCCGGGCATGGTGGCACGCGCCTGTAATCCCAGCTACTCTGGAGGCTG AAGAAAAAAAAAAATTAGCCGGGCATGGTGGCTCGCGCCTGTAATCCCAGCTACTCTGGAGGCTG A T ADGRB3 Ensembl:ENSG00000135298 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1042910508 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91695,RMVar_hsa_circ_239265 32094 RMVar_ID_32094 Human_SNP_ID_281242233 A-to-I Human chr6 + 68706854 68706854 68706854 TTGATGGAGGCTGGGCGTGGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCCGAGGCAAGC TTGATGGAGGCTGGGCGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAAGC A G ADGRB3 Ensembl:ENSG00000135298 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1466490298 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91695,RMVar_hsa_circ_239265,RMVar_hsa_circ_239269 32095 RMVar_ID_32095 Human_SNP_ID_281249588 A-to-I Human chr6 + 68738021 68738021 68738021 GAAAGGGAAAGGTGTTGCTAGGGAGAATGGACAAGTTTGACTAAAGTGATCAAGAAAGACCTTAC GAAAGGGAAAGGTGTTGCTAGGGAGAATGGACGAGTTTGACTAAAGTGATCAAGAAAGACCTTAC A G ADGRB3 Ensembl:ENSG00000135298 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs780505861 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15867288 RMVar_hsa_circ_91695,RMVar_hsa_circ_239265,RMVar_hsa_circ_239274 32096 RMVar_ID_32096 Human_SNP_ID_281257107 A-to-I Human chr6 + 68769343 68769343 68769343 TGGATAAATAAAATATGGCACATATACACCATAGAATACTATGCAGCCATAAAAAAGATGAGTTC TGGATAAATAAAATATGGCACATATACACCATGGAATACTATGCAGCCATAAAAAAGATGAGTTC A G ADGRB3 Ensembl:ENSG00000135298 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1037186182 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91695,RMVar_hsa_circ_239265 32097 RMVar_ID_32097 Human_SNP_ID_281280150 A-to-I Human chr6 + 68856597 68856597 68856597 GAACTTGAGAGAGATAATTTAGAATACCTGGCAGAAGAAATTTCTAAACAGCAAAGCATTCAATA GAACTTGAGAGAGATAATTTAGAATACCTGGCGGAAGAAATTTCTAAACAGCAAAGCATTCAATA A G ADGRB3 Ensembl:ENSG00000135298 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs980781818 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91695,RMVar_hsa_circ_239265 32098 RMVar_ID_32098 Human_SNP_ID_281281007 A-to-I Human chr6 + 68859557 68859557 68859557 GACATTGCTTGAGAGGCCTCACAATTATGGCTAAAGACAAAGGAATAGCAAAGGGATGTCTTACA GACATTGCTTGAGAGGCCTCACAATTATGGCTGAAGACAAAGGAATAGCAAAGGGATGTCTTACA A G ADGRB3 Ensembl:ENSG00000135298 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1412950298 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91695,RMVar_hsa_circ_239265 32099 RMVar_ID_32099 Human_SNP_ID_281283389 A-to-I Human chr6 + 68868177 68868177 68868177 ATAATCCCCATATGTCAGGGAAGGGACATGGTAGGAAGTGACTGGATCATGGGGGAGGTTTCCCC ATAATCCCCATATGTCAGGGAAGGGACATGGTTGGAAGTGACTGGATCATGGGGGAGGTTTCCCC A T ADGRB3 Ensembl:ENSG00000135298 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1282344196 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91695,RMVar_hsa_circ_239265 32100 RMVar_ID_32100 Human_SNP_ID_281286276 A-to-I Human chr6 + 68878966 68878966 68878966 AGACTTACTCACTATCAGGAGAACAGCACAGGAAAGACCTGTGCCCATGATTCAAGCATCTCCCA AGACTTACTCACTATCAGGAGAACAGCACAGGGAAGACCTGTGCCCATGATTCAAGCATCTCCCA A G ADGRB3 Ensembl:ENSG00000135298 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1198001390 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91695,RMVar_hsa_circ_239265 32101 RMVar_ID_32101 Human_SNP_ID_281304940 A-to-I Human chr6 + 68950166 68950166 68950166 TACCTGGGAATCCTGGGCTCAAGCATCCTCCCACCTCAGCCTCTTGAGTAGCTGAGACTACAGGT TACCTGGGAATCCTGGGCTCAAGCATCCTCCCGCCTCAGCCTCTTGAGTAGCTGAGACTACAGGT A G ADGRB3 Ensembl:ENSG00000135298 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1208981587 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3089,RMVar_hsa_circ_275786,RMVar_hsa_circ_310690,RMVar_hsa_circ_321446,RMVar_hsa_circ_313228,RMVar_hsa_circ_301771,RMVar_hsa_circ_307700,RMVar_hsa_circ_292934,RMVar_hsa_circ_287561,RMVar_hsa_circ_289324,RMVar_hsa_circ_45501,RMVar_hsa_circ_99653,RMVar_hsa_circ_11186,RMVar_hsa_circ_239289,RMVar_hsa_circ_239281,RMVar_hsa_circ_239283,RMVar_hsa_circ_239285,RMVar_hsa_circ_239286,RMVar_hsa_circ_239284,RMVar_hsa_circ_239282,RMVar_hsa_circ_239279,RMVar_hsa_circ_239280,RMVar_hsa_circ_266986,RMVar_hsa_circ_268725,RMVar_hsa_circ_376657,RMVar_hsa_circ_11969,RMVar_hsa_circ_239291,RMVar_hsa_circ_239295,RMVar_hsa_circ_307135,RMVar_hsa_circ_336072,RMVar_hsa_circ_342824,RMVar_hsa_circ_376849,RMVar_hsa_circ_315168,RMVar_hsa_circ_290142,RMVar_hsa_circ_302879,RMVar_hsa_circ_239296,RMVar_hsa_circ_239293,RMVar_hsa_circ_239294,RMVar_hsa_circ_239292,RMVar_hsa_circ_239290 32102 RMVar_ID_32102 Human_SNP_ID_281346602 A-to-I Human chr6 + 69110077 69110077 69110077 TCAAGCGATTCTCCTGCCTCAGCACCCCGAGTAGCTGGGATTACAGGCGCCTGCCACCACGACTG TCAAGCGATTCTCCTGCCTCAGCACCCCGAGTGGCTGGGATTACAGGCGCCTGCCACCACGACTG A G ADGRB3 Ensembl:ENSG00000135298 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs953978511 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3089,RMVar_hsa_circ_321446,RMVar_hsa_circ_307700,RMVar_hsa_circ_45501,RMVar_hsa_circ_99653,RMVar_hsa_circ_11186,RMVar_hsa_circ_239305,RMVar_hsa_circ_37219,RMVar_hsa_circ_239279,RMVar_hsa_circ_239280,RMVar_hsa_circ_84780,RMVar_hsa_circ_94199,RMVar_hsa_circ_239306,RMVar_hsa_circ_26808,RMVar_hsa_circ_340693,RMVar_hsa_circ_239318,RMVar_hsa_circ_304759,RMVar_hsa_circ_335648,RMVar_hsa_circ_279422 32103 RMVar_ID_32103 Human_SNP_ID_281347873 A-to-I Human chr6 + 69115165 69115165 69115165 GACACATGCACATGTATGTTTATTGCAACACTATTCCCAATAGCAAAGACTTGGAACCAACCCAA GACACATGCACATGTATGTTTATTGCAACACTGTTCCCAATAGCAAAGACTTGGAACCAACCCAA A G ADGRB3 Ensembl:ENSG00000135298 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1400503520 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3089,RMVar_hsa_circ_321446,RMVar_hsa_circ_307700,RMVar_hsa_circ_45501,RMVar_hsa_circ_99653,RMVar_hsa_circ_11186,RMVar_hsa_circ_239305,RMVar_hsa_circ_37219,RMVar_hsa_circ_239279,RMVar_hsa_circ_239280,RMVar_hsa_circ_84780,RMVar_hsa_circ_94199,RMVar_hsa_circ_239306,RMVar_hsa_circ_26808,RMVar_hsa_circ_340693,RMVar_hsa_circ_239318,RMVar_hsa_circ_304759,RMVar_hsa_circ_335648,RMVar_hsa_circ_279422 32104 RMVar_ID_32104 Human_SNP_ID_281405251 A-to-I Human chr6 + 69341390 69341390 69341390 AATGACCAGTGATGATGATCTATTTTTCATATATTTGTTGGCTGCATAAATGTCTTAATAAGATA AATGACCAGTGATGATGATCTATTTTTCATATGTTTGTTGGCTGCATAAATGTCTTAATAAGATA A G ADGRB3 Ensembl:ENSG00000135298 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1319481913 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3089,RMVar_hsa_circ_11186,RMVar_hsa_circ_239305,RMVar_hsa_circ_84780,RMVar_hsa_circ_328278,RMVar_hsa_circ_25814,RMVar_hsa_circ_1295,RMVar_hsa_circ_345294,RMVar_hsa_circ_2273,RMVar_hsa_circ_239337,RMVar_hsa_circ_24676,RMVar_hsa_circ_377796,RMVar_hsa_circ_336890,RMVar_hsa_circ_239338,RMVar_hsa_circ_330659,RMVar_hsa_circ_14440,RMVar_hsa_circ_291232,RMVar_hsa_circ_239339,RMVar_hsa_circ_239340,RMVar_hsa_circ_318857,RMVar_hsa_circ_378563,RMVar_hsa_circ_239341,RMVar_hsa_circ_239342,RMVar_hsa_circ_239343,RMVar_hsa_circ_338908,RMVar_hsa_circ_239344 32105 RMVar_ID_32105 Human_SNP_ID_281406617 A-to-I Human chr6 + 69346617 69346617 69346617 AACAAACATATGAAAAATAGCTCATCATCACTAGTCATTAGAGAAATGCAAATCAAAACCTCAGT AACAAACATATGAAAAATAGCTCATCATCACTGGTCATTAGAGAAATGCAAATCAAAACCTCAGT A G ADGRB3 Ensembl:ENSG00000135298 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1252363835 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3089,RMVar_hsa_circ_11186,RMVar_hsa_circ_239305,RMVar_hsa_circ_84780,RMVar_hsa_circ_328278,RMVar_hsa_circ_25814,RMVar_hsa_circ_1295,RMVar_hsa_circ_345294,RMVar_hsa_circ_2273,RMVar_hsa_circ_239337,RMVar_hsa_circ_24676,RMVar_hsa_circ_377796,RMVar_hsa_circ_336890,RMVar_hsa_circ_239338,RMVar_hsa_circ_330659,RMVar_hsa_circ_14440,RMVar_hsa_circ_291232,RMVar_hsa_circ_239339,RMVar_hsa_circ_239340,RMVar_hsa_circ_318857,RMVar_hsa_circ_378563,RMVar_hsa_circ_239341,RMVar_hsa_circ_239342,RMVar_hsa_circ_239343,RMVar_hsa_circ_338908,RMVar_hsa_circ_239344 32106 RMVar_ID_32106 Human_SNP_ID_281407917 A-to-I Human chr6 + 69351173 69351173 69351173 TGGAGTACAATGGCACAATCTCGGCTCACTGCAACCTTCGCCTCCCGAGTTCAAGCAATTCTCCT TGGAGTACAATGGCACAATCTCGGCTCACTGCGACCTTCGCCTCCCGAGTTCAAGCAATTCTCCT A G ADGRB3 Ensembl:ENSG00000135298 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1171741631 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3089,RMVar_hsa_circ_11186,RMVar_hsa_circ_239305,RMVar_hsa_circ_84780,RMVar_hsa_circ_328278,RMVar_hsa_circ_25814,RMVar_hsa_circ_1295,RMVar_hsa_circ_345294,RMVar_hsa_circ_2273,RMVar_hsa_circ_239337,RMVar_hsa_circ_24676,RMVar_hsa_circ_377796,RMVar_hsa_circ_336890,RMVar_hsa_circ_239338,RMVar_hsa_circ_330659,RMVar_hsa_circ_14440,RMVar_hsa_circ_291232,RMVar_hsa_circ_239339,RMVar_hsa_circ_239340,RMVar_hsa_circ_318857,RMVar_hsa_circ_378563,RMVar_hsa_circ_239341,RMVar_hsa_circ_239342,RMVar_hsa_circ_239343,RMVar_hsa_circ_338908,RMVar_hsa_circ_239344 32107 RMVar_ID_32107 Human_SNP_ID_281687540 A-to-I Human chr6 + 70441265 70441265 70441265 AAAATACAAAAATTAGCCGGTGGCACGCACCTATAATCCCAGCTACTCAGGAGGCTGAGATGGGA AAAATACAAAAATTAGCCGGTGGCACGCACCTGTAATCCCAGCTACTCAGGAGGCTGAGATGGGA A G FAM135A Ensembl:ENSG00000082269 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs550843997 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23462,RMVar_hsa_circ_239374,RMVar_hsa_circ_271307,RMVar_hsa_circ_317149,RMVar_hsa_circ_291271,RMVar_hsa_circ_52415,RMVar_hsa_circ_47054,RMVar_hsa_circ_33984,RMVar_hsa_circ_65136,RMVar_hsa_circ_317317,RMVar_hsa_circ_239375,RMVar_hsa_circ_239376,RMVar_hsa_circ_239377,RMVar_hsa_circ_318087,RMVar_hsa_circ_290758,RMVar_hsa_circ_297273,RMVar_hsa_circ_68378,RMVar_hsa_circ_239379,RMVar_hsa_circ_239380,RMVar_hsa_circ_239381,RMVar_hsa_circ_318182,RMVar_hsa_circ_304352,RMVar_hsa_circ_289392,RMVar_hsa_circ_239382,RMVar_hsa_circ_239383,RMVar_hsa_circ_335577,RMVar_hsa_circ_357726,RMVar_hsa_circ_309850,RMVar_hsa_circ_62036,RMVar_hsa_circ_69903,RMVar_hsa_circ_54206,RMVar_hsa_circ_30055,RMVar_hsa_circ_31317,RMVar_hsa_circ_239386,RMVar_hsa_circ_239387,RMVar_hsa_circ_239388,RMVar_hsa_circ_239385 32108 RMVar_ID_32108 Human_SNP_ID_281720105 A-to-I Human chr6 + 70573532 70573532 70573532 GTGATCCACCTGCCTCAGCCTCCCAAATTGCTAGGATTACAGGTGTGAGCCACAATGCCCGGCCA GTGATCCACCTGCCTCAGCCTCCCAAATTGCTGGGATTACAGGTGTGAGCCACAATGCCCGGCCA A G SDHAF4 Ensembl:ENSG00000154079 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1180503517 Functional Loss SNV dbSNP153 33..33 33 - - - 32109 RMVar_ID_32109 Human_SNP_ID_281723743 A-to-I Human chr6 + 70588936 70588936 70588936 CAGCCTGACCAATATGGAGAAATCTCGCCTTTACTAAAAATACAAAATTAGCCAGGCGTGGTGGC CAGCCTGACCAATATGGAGAAATCTCGCCTTTGCTAAAAATACAAAATTAGCCAGGCGTGGTGGC A G SDHAF4 Ensembl:ENSG00000154079 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1292987006 Functional Loss SNV dbSNP153 33..33 33 - - - 32110 RMVar_ID_32110 Human_SNP_ID_281723763 A-to-I Human chr6 + 70588989 70588989 70588989 AGGCGTGGTGGCATGCACCTGTAATCCCAACTACTCTGGAGGCTGAGGCAGGAGAATGGCTTAAA AGGCGTGGTGGCATGCACCTGTAATCCCAACTGCTCTGGAGGCTGAGGCAGGAGAATGGCTTAAA A G SDHAF4 Ensembl:ENSG00000154079 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1457677922 Functional Loss SNV dbSNP153 33..33 33 - - - 32111 RMVar_ID_32111 Human_SNP_ID_281723771 A-to-I Human chr6 + 70589019 70589019 70589019 CTACTCTGGAGGCTGAGGCAGGAGAATGGCTTAAACCCAGGAGGTGGAGGTTGCGGTGAGCTGAG CTACTCTGGAGGCTGAGGCAGGAGAATGGCTTGAACCCAGGAGGTGGAGGTTGCGGTGAGCTGAG A G SDHAF4 Ensembl:ENSG00000154079 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1346407507 Functional Loss SNV dbSNP153 33..33 33 - - - 32112 RMVar_ID_32112 Human_SNP_ID_281723884 A-to-I Human chr6 + 70589283 70589283 70589283 GCCCCGCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGACACCCA GCCCCGCCAGGTTCAAGCAATTCTCCTGCCTCCGCCTCCTGAGTAGCTGGGATTACAGACACCCA A C SDHAF4 Ensembl:ENSG00000154079 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1225573814 Functional Loss SNV dbSNP153 33..33 33 - - - 32113 RMVar_ID_32113 Human_SNP_ID_281723903 A-to-I Human chr6 + 70589355 70589355 70589355 GCCTGGCTAATTTTTGTATTTTTAGTAAAGACAAGGTTTCACCATGTTAGCCAGGCTGGTCTCGA GCCTGGCTAATTTTTGTATTTTTAGTAAAGACGAGGTTTCACCATGTTAGCCAGGCTGGTCTCGA A G SDHAF4 Ensembl:ENSG00000154079 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1197221130 Functional Loss SNV dbSNP153 33..33 33 - - - 32114 RMVar_ID_32114 Human_SNP_ID_281931858 A-to-I Human chr6 - 71410004 71410004 71410004 TATCTCTGTCGCTCAAGCTGGAGTTCAGTGGCATGAACAGGGCTCATTGCAGCCTCAACCTTCCA TATCTCTGTCGCTCAAGCTGGAGTTCAGTGGCGTGAACAGGGCTCATTGCAGCCTCAACCTTCCA T C LINC00472,AL136164.2 Ensembl:ENSG00000233237,Ensembl:ENSG00000269966 lincRNA,lincRNA intron,intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs773191260 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15871499 32115 RMVar_ID_32115 Human_SNP_ID_281931869 A-to-I Human chr6 - 71410035 71410035 71410035 AGATTTTTTTTTTTCTTTTTTTGAGTCAGGTTATCTCTGTCGCTCAAGCTGGAGTTCAGTGGCAT AGATTTTTTTTTTTCTTTTTTTGAGTCAGGTTCTCTCTGTCGCTCAAGCTGGAGTTCAGTGGCAT T G LINC00472,AL136164.2 Ensembl:ENSG00000233237,Ensembl:ENSG00000269966 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1342113265 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3016775,Human_RBP_ID_10294092,Human_RBP_ID_15941658 32116 RMVar_ID_32116 Human_SNP_ID_282077338 A-to-I Human chr6 + 71989870 71989870 71989870 TCCTGCATGACCTGGCCTAAGCCTGCTCCTCCAACCCCACCTCAGGCCACACTAACCCTCACTCA TCCTGCATGACCTGGCCTAAGCCTGCTCCTCCGACCCCACCTCAGGCCACACTAACCCTCACTCA A G RIMS1 Ensembl:ENSG00000079841 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1296088551 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_239425,RMVar_hsa_circ_44547,RMVar_hsa_circ_96214,RMVar_hsa_circ_239426 32117 RMVar_ID_32117 Human_SNP_ID_282093129 A-to-I Human chr6 + 72054092 72054092 72054092 TTGCTCTCCCTCCCCTTGCCCACCACCCCCCAAACTGGCCCTGGTATGTGTTGTTCCCCTCCCTT TTGCTCTCCCTCCCCTTGCCCACCACCCCCCAGACTGGCCCTGGTATGTGTTGTTCCCCTCCCTT A G RIMS1 Ensembl:ENSG00000079841 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs899877625 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44547,RMVar_hsa_circ_96214,RMVar_hsa_circ_239426 32118 RMVar_ID_32118 Human_SNP_ID_282093130 A-to-I Human chr6 + 72054092 72054092 72054092 TTGCTCTCCCTCCCCTTGCCCACCACCCCCCAAACTGGCCCTGGTATGTGTTGTTCCCCTCCCTT TTGCTCTCCCTCCCCTTGCCCACCACCCCCCATACTGGCCCTGGTATGTGTTGTTCCCCTCCCTT A T RIMS1 Ensembl:ENSG00000079841 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs899877625 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44547,RMVar_hsa_circ_96214,RMVar_hsa_circ_239426 32119 RMVar_ID_32119 Human_SNP_ID_282093152 A-to-I Human chr6 + 72054158 72054158 72054158 GTCCATTCGTTCTCATTGTTCATCTCCTACTTATGAGTGAGAAAACGTGGTGTTTGGTTTTCTGT GTCCATTCGTTCTCATTGTTCATCTCCTACTTTTGAGTGAGAAAACGTGGTGTTTGGTTTTCTGT A T RIMS1 Ensembl:ENSG00000079841 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1380297393 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44547,RMVar_hsa_circ_96214,RMVar_hsa_circ_239426 32120 RMVar_ID_32120 Human_SNP_ID_282093199 A-to-I Human chr6 + 72054366 72054366 72054366 GCATTTGGGTTGGTTCCATGTCTTTGTATTGTAAACAGTGCTGCAATAAACATATGTGTGCATGT GCATTTGGGTTGGTTCCATGTCTTTGTATTGTGAACAGTGCTGCAATAAACATATGTGTGCATGT A G RIMS1 Ensembl:ENSG00000079841 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs573671358 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44547,RMVar_hsa_circ_96214,RMVar_hsa_circ_239426 32121 RMVar_ID_32121 Human_SNP_ID_282093591 A-to-I Human chr6 + 72055982 72055982 72055982 GACACATGCATGCATATGTTCATCGCAGCAGTATTCACGATAGCAAAGATATGAAATAAACCTAA GACACATGCATGCATATGTTCATCGCAGCAGTGTTCACGATAGCAAAGATATGAAATAAACCTAA A G RIMS1 Ensembl:ENSG00000079841 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1361585709 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44547,RMVar_hsa_circ_96214,RMVar_hsa_circ_239426 32122 RMVar_ID_32122 Human_SNP_ID_282105729 A-to-I Human chr6 + 72107292 72107292 72107292 GATAATAGAAATGAAACCCCACCAGGAGCGGTAGCTCACGCCTGTAATCCCAGCACTTTGGGAGG GATAATAGAAATGAAACCCCACCAGGAGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGG A G RIMS1 Ensembl:ENSG00000079841 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1262954181 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44547,RMVar_hsa_circ_3346,RMVar_hsa_circ_239433 32123 RMVar_ID_32123 Human_SNP_ID_282106035 A-to-I Human chr6 + 72108438 72108438 72108438 AATTGTTACTCTTTGACTACATCATCACCACTAAACTATTTTAAGAAACAAAACAATACTATCAC AATTGTTACTCTTTGACTACATCATCACCACTGAACTATTTTAAGAAACAAAACAATACTATCAC A G RIMS1 Ensembl:ENSG00000079841 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs951257540 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44547,RMVar_hsa_circ_3346,RMVar_hsa_circ_239433 32124 RMVar_ID_32124 Human_SNP_ID_282150178 A-to-I Human chr6 + 72287835 72287835 72287835 AGGCTGCTCTTGAACTCCTGACCTTATGATCCACCCGCCTCAGCCTCCCATAGTGGCATGAGCCA AGGCTGCTCTTGAACTCCTGACCTTATGATCCCCCCGCCTCAGCCTCCCATAGTGGCATGAGCCA A C RIMS1 Ensembl:ENSG00000079841 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs939999777 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44547,RMVar_hsa_circ_25779,RMVar_hsa_circ_3346,RMVar_hsa_circ_41788,RMVar_hsa_circ_320178,RMVar_hsa_circ_343156,RMVar_hsa_circ_322795,RMVar_hsa_circ_300002,RMVar_hsa_circ_239440,RMVar_hsa_circ_301332,RMVar_hsa_circ_307547,RMVar_hsa_circ_331868,RMVar_hsa_circ_6455,RMVar_hsa_circ_239444,RMVar_hsa_circ_239445,RMVar_hsa_circ_239446,RMVar_hsa_circ_337952,RMVar_hsa_circ_306435,RMVar_hsa_circ_239448,RMVar_hsa_circ_239447,RMVar_hsa_circ_239453,RMVar_hsa_circ_312001,RMVar_hsa_circ_268718,RMVar_hsa_circ_268399,RMVar_hsa_circ_117418,RMVar_hsa_circ_239456,RMVar_hsa_circ_323578,RMVar_hsa_circ_313069,RMVar_hsa_circ_10980,RMVar_hsa_circ_239457,RMVar_hsa_circ_38784,RMVar_hsa_circ_31372,RMVar_hsa_circ_265826,RMVar_hsa_circ_303408,RMVar_hsa_circ_307739,RMVar_hsa_circ_301695,RMVar_hsa_circ_239465,RMVar_hsa_circ_239466,RMVar_hsa_circ_239464 32125 RMVar_ID_32125 Human_SNP_ID_282165704 A-to-I Human chr6 + 72353070 72353070 72353070 TGGAGTGCAATGGCGAGATCTCGGCTCACTGCAACTTCCGTCTCCCGGGTTCAAGTGATTCTCCT TGGAGTGCAATGGCGAGATCTCGGCTCACTGCGACTTCCGTCTCCCGGGTTCAAGTGATTCTCCT A G RIMS1 Ensembl:ENSG00000079841 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1382434185 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15908,RMVar_hsa_circ_34378 32126 RMVar_ID_32126 Human_SNP_ID_282237108 A-to-I Human chr6 + 72643586 72643586 72643586 ATTCTCAAAGGAAATGCTCATCGGAGCATTTCAGATTTTGGATTTTGGATTAGGGATGCTCAAAC ATTCTCAAAGGAAATGCTCATCGGAGCATTTCGGATTTTGGATTTTGGATTAGGGATGCTCAAAC A G KCNQ5-IT1,KCNQ5 Ensembl:ENSG00000233844,Ensembl:ENSG00000185760 lincRNA,Protein coding intron,intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs898155358 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8270852 RMVar_hsa_circ_72842,RMVar_hsa_circ_239479 32127 RMVar_ID_32127 Human_SNP_ID_282242831 A-to-I Human chr6 + 72668835 72668835 72668835 GGGCCTCCTCAGTAACCACATCAGCCAGCACCAAGATCTGAAACTTCCAGCCTTCTTAGAAGGAC GGGCCTCCTCAGTAACCACATCAGCCAGCACCGAGATCTGAAACTTCCAGCCTTCTTAGAAGGAC A G KCNQ5-IT1,KCNQ5 Ensembl:ENSG00000233844,Ensembl:ENSG00000185760 lincRNA,Protein coding intron,intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1017664790 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72842 32128 RMVar_ID_32128 Human_SNP_ID_282267170 A-to-I Human chr6 + 72778480 72778480 72778480 GGGGTCGCTTGACCCCCAGAGGAGGGGACTGCAATGAGCAGAGATCACGCCACTGCACTCCAGCC GGGGTCGCTTGACCCCCAGAGGAGGGGACTGCGATGAGCAGAGATCACGCCACTGCACTCCAGCC A G KCNQ5 Ensembl:ENSG00000185760 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1289512610 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23315004 32129 RMVar_ID_32129 Human_SNP_ID_282273474 A-to-I Human chr6 + 72806419 72806419 72806419 CTTGAGGAAGTAGGAATGGGAACCCAGTACTGAAGTTATAGGCCAAATCAAAAGATGGGAAATCT CTTGAGGAAGTAGGAATGGGAACCCAGTACTGCAGTTATAGGCCAAATCAAAAGATGGGAAATCT A C KCNQ5 Ensembl:ENSG00000185760 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1450096986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26020123 32130 RMVar_ID_32130 Human_SNP_ID_282370255 A-to-I Human chr6 - 73226355 73226355 73226355 TCACTGCAACCTCTGCCTCCCGGCTTCAAGCGATTCTCCTGCTGCAGCCTCCTGAGTAACTGGAA TCACTGCAACCTCTGCCTCCCGGCTTCAAGCGTTTCTCCTGCTGCAGCCTCCTGAGTAACTGGAA T A AL365232.1 Ensembl:ENSG00000243501 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215474415 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267 32131 RMVar_ID_32131 Human_SNP_ID_282381034 A-to-I Human chr6 - 73270433 73270433 73270433 GGAGTCCCGCTCTGTTGCCCAGGTTGGAGTGTAGTCGCAAAATCTCAGCTCACTGCAACCTCTGC GGAGTCCCGCTCTGTTGCCCAGGTTGGAGTGTGGTCGCAAAATCTCAGCTCACTGCAACCTCTGC T C KHDC1 Ensembl:ENSG00000135314 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs953713651 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22616790 32132 RMVar_ID_32132 Human_SNP_ID_282381035 A-to-I Human chr6 + 73270434 73270434 73270434 CAGAGGTTGCAGTGAGCTGAGATTTTGCGACTACACTCCAACCTGGGCAACAGAGCGGGACTCCA CAGAGGTTGCAGTGAGCTGAGATTTTGCGACTGCACTCCAACCTGGGCAACAGAGCGGGACTCCA A G AC019205.1 Ensembl:ENSG00000229852 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1189853369 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8270813,Human_RBP_ID_8648671,Human_RBP_ID_26020569 Human_Splice_Rec_786396,Human_Splice_Rec_786397,Human_Splice_Rec_786400,Human_Splice_Rec_786401,Human_Splice_Rec_786406,Human_Splice_Rec_786407,Human_Splice_Rec_786413 32133 RMVar_ID_32133 Human_SNP_ID_282381600 A-to-I Human chr6 + 73272514 73272514 73272514 AGCCAGGTAGAAGGCCAGACGTGGTGGCTCACACCCGTAATCCCAGCGCTTTGGGAGGCTGAGGT AGCCAGGTAGAAGGCCAGACGTGGTGGCTCACCCCCGTAATCCCAGCGCTTTGGGAGGCTGAGGT A C AC019205.1 Ensembl:ENSG00000229852 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444771652 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5250910 32134 RMVar_ID_32134 Human_SNP_ID_282381601 A-to-I Human chr6 + 73272514 73272514 73272514 AGCCAGGTAGAAGGCCAGACGTGGTGGCTCACACCCGTAATCCCAGCGCTTTGGGAGGCTGAGGT AGCCAGGTAGAAGGCCAGACGTGGTGGCTCACGCCCGTAATCCCAGCGCTTTGGGAGGCTGAGGT A G AC019205.1 Ensembl:ENSG00000229852 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444771652 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5250910 32135 RMVar_ID_32135 Human_SNP_ID_282381622 A-to-I Human chr6 + 73272584 73272584 73272584 TATCACTTCAGATCGGAGTTCCAGACCAGCCTAGCCAACATGGTAAGACCCTGTCTCTACTAAAA TATCACTTCAGATCGGAGTTCCAGACCAGCCTTGCCAACATGGTAAGACCCTGTCTCTACTAAAA A T AC019205.1 Ensembl:ENSG00000229852 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037064642 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8271271 32136 RMVar_ID_32136 Human_SNP_ID_282383483 A-to-I Human chr6 + 73279769 73279768 73279770 ACCCAGCTAATGTTTATATTTTTCGTAGAGACAGAGTTTTGCTGTGTTGCCAGGCTGATCAACTC ACCCAGCTAATGTTTATATTTTTCGTAGAGAC__AGTTTTGCTGTGTTGCCAGGCTGATCAACTC CAG C AC019205.1 Ensembl:ENSG00000229852 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1406502604 Functional Loss DEL dbSNP153 33..34 33 - - - 32137 RMVar_ID_32137 Human_SNP_ID_282386716 A-to-I Human chr6 - 73292430 73292430 73292430 ACTTACAGCATTTCTGTCTGTTGCTGGAACCAACACTCTGAAAAAATAAAGATATTCTGCTGCTC ACTTACAGCATTTCTGTCTGTTGCTGGAACCAGCACTCTGAAAAAATAAAGATATTCTGCTGCTC T C KHDC1 Ensembl:ENSG00000135314 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs183513861 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1675809,Human_RBP_ID_3814536 32138 RMVar_ID_32138 Human_SNP_ID_282419456 A-to-I Human chr6 - 73419249 73419248 73419249 CGCCACCATGCCTGGCTAATTTTCATATTTTTAGTAGAGACGGGGTTTCACCACGTTGGGCAGGC CGCCACCATGCCTGGCTAATTTTCATATTTTT_GTAGAGACGGGGTTTCACCACGTTGGGCAGGC CT C CGAS Ensembl:ENSG00000164430 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1173273715 Functional Loss DEL dbSNP153 33..33 33 - - - 32139 RMVar_ID_32139 Human_SNP_ID_282419817 A-to-I Human chr6 - 73420694 73420694 73420694 ATTTTTTGTATTTTTAGTAGAGACAGGGTTTCACTATGTTGGCCAGGCTGGTCTTGAATGCTTGA ATTTTTTGTATTTTTAGTAGAGACAGGGTTTCTCTATGTTGGCCAGGCTGGTCTTGAATGCTTGA T A CGAS Ensembl:ENSG00000164430 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1014463799 Functional Loss SNV dbSNP153 33..33 33 - - - 32140 RMVar_ID_32140 Human_SNP_ID_282419819 A-to-I Human chr6 - 73420702 73420700 73420702 CCCACCTAATTTTTTGTATTTTTAGTAGAGACAGGGTTTCACTATGTTGGCCAGGCTGGTCTTGA CCCACCTAATTTTTTGTATTTTTAGTAGAGAC__GGTTTCACTATGTTGGCCAGGCTGGTCTTGA CCT C CGAS Ensembl:ENSG00000164430 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs994214640 Functional Loss DEL dbSNP153 33..34 33 - - - 32141 RMVar_ID_32141 Human_SNP_ID_282419910 A-to-I Human chr6 - 73421013 73421013 73421013 TGAGGCAGAAGAATTGCTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCCGAGATTGTGCCATTGC TGAGGCAGAAGAATTGCTTGAACCTGGGAGGCGGAGGTTGCAGTGAGCCGAGATTGTGCCATTGC T C CGAS Ensembl:ENSG00000164430 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1410932585 Functional Loss SNV dbSNP153 33..33 33 - - - 32142 RMVar_ID_32142 Human_SNP_ID_282420464 A-to-I Human chr6 - 73423477 73423477 73423477 CTCACTGCACCCTCCTCCTCCCGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGA CTCACTGCACCCTCCTCCTCCCGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGA T C CGAS Ensembl:ENSG00000164430 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1021251993 Functional Loss SNV dbSNP153 33..33 33 - - - 32143 RMVar_ID_32143 Human_SNP_ID_282420669 A-to-I Human chr6 - 73424245 73424245 73424245 TATTTTTAGTAAAGATGGGGTTTCACCATGTTAGCCAGGATGGTCTCGATCTCCTTACCTTGTGA TATTTTTAGTAAAGATGGGGTTTCACCATGTTTGCCAGGATGGTCTCGATCTCCTTACCTTGTGA T A CGAS Ensembl:ENSG00000164430 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229,31158229 RNA-Seq:(High) rs552409705 Functional Loss SNV dbSNP153 33..33 33 - - - 32144 RMVar_ID_32144 Human_SNP_ID_282420670 A-to-I Human chr6 - 73424245 73424245 73424245 TATTTTTAGTAAAGATGGGGTTTCACCATGTTAGCCAGGATGGTCTCGATCTCCTTACCTTGTGA TATTTTTAGTAAAGATGGGGTTTCACCATGTTGGCCAGGATGGTCTCGATCTCCTTACCTTGTGA T C CGAS Ensembl:ENSG00000164430 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229,31158229 RNA-Seq:(High) rs552409705 Functional Loss SNV dbSNP153 33..33 33 - - - 32145 RMVar_ID_32145 Human_SNP_ID_282420671 A-to-I Human chr6 - 73424245 73424245 73424245 TATTTTTAGTAAAGATGGGGTTTCACCATGTTAGCCAGGATGGTCTCGATCTCCTTACCTTGTGA TATTTTTAGTAAAGATGGGGTTTCACCATGTTCGCCAGGATGGTCTCGATCTCCTTACCTTGTGA T G CGAS Ensembl:ENSG00000164430 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229,31158229 RNA-Seq:(High) rs552409705 Functional Loss SNV dbSNP153 33..33 33 - - - 32146 RMVar_ID_32146 Human_SNP_ID_282420685 A-to-I Human chr6 - 73424266 73424266 73424266 CCACATCCGGCTAATTTTTTGTATTTTTAGTAAAGATGGGGTTTCACCATGTTAGCCAGGATGGT CCACATCCGGCTAATTTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTAGCCAGGATGGT T C CGAS Ensembl:ENSG00000164430 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs370053803 Functional Loss SNV dbSNP153 33..33 33 - - - 32147 RMVar_ID_32147 Human_SNP_ID_282420686 A-to-I Human chr6 - 73424266 73424266 73424266 CCACATCCGGCTAATTTTTTGTATTTTTAGTAAAGATGGGGTTTCACCATGTTAGCCAGGATGGT CCACATCCGGCTAATTTTTTGTATTTTTAGTACAGATGGGGTTTCACCATGTTAGCCAGGATGGT T G CGAS Ensembl:ENSG00000164430 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs370053803 Functional Loss SNV dbSNP153 33..33 33 - - - 32148 RMVar_ID_32148 Human_SNP_ID_282420848 A-to-I Human chr6 - 73424914 73424894 73424915 AGGAGGTGGAGGTTGCAGTGAGTCAAGATGGCACCACTGCACTCCATCCTGGGTGACAGAGCAAG AGGAGGTGGAGGTTGCAGTGAGTCAAGATGG_____________________GTGACAGAGCAAG CCCAGGATGGAGTGCAGTGGTG C CGAS Ensembl:ENSG00000164430 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1441984214 Functional Loss DEL dbSNP153 32..52 33 - - - Human_RBP_ID_15874732 32149 RMVar_ID_32149 Human_SNP_ID_282420852 A-to-I Human chr6 - 73424914 73424914 73424914 AGGAGGTGGAGGTTGCAGTGAGTCAAGATGGCACCACTGCACTCCATCCTGGGTGACAGAGCAAG AGGAGGTGGAGGTTGCAGTGAGTCAAGATGGCGCCACTGCACTCCATCCTGGGTGACAGAGCAAG T C CGAS Ensembl:ENSG00000164430 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1207268761 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15874732 32150 RMVar_ID_32150 Human_SNP_ID_282420868 A-to-I Human chr6 - 73424982 73424982 73424982 GGGCATGGTGATGCATGCCTGTAATCCCAGCTACTCGGGAGGCTTAGACATGAGAATCACTTGAA GGGCATGGTGATGCATGCCTGTAATCCCAGCTGCTCGGGAGGCTTAGACATGAGAATCACTTGAA T C CGAS Ensembl:ENSG00000164430 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1252679580 Functional Loss SNV dbSNP153 33..33 33 - - - 32151 RMVar_ID_32151 Human_SNP_ID_282420880 A-to-I Human chr6 - 73425058 73425058 73425058 CTTGAGGTCAGGAGTTTGAGACCAGCCTGACCAACATGGTGAAACTCCATCTCTACTAAAAATAT CTTGAGGTCAGGAGTTTGAGACCAGCCTGACCGACATGGTGAAACTCCATCTCTACTAAAAATAT T C CGAS Ensembl:ENSG00000164430 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs951590187 Functional Loss SNV dbSNP153 33..33 33 - - - 32152 RMVar_ID_32152 Human_SNP_ID_282420897 A-to-I Human chr6 - 73425132 73425132 73425132 AATTTGAAAAGGGGCCAGACGCTGTGGCTCACACCTGTAATCCCAGCTCTTTGGAGGCCGAGGCA AATTTGAAAAGGGGCCAGACGCTGTGGCTCACGCCTGTAATCCCAGCTCTTTGGAGGCCGAGGCA T C CGAS Ensembl:ENSG00000164430 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs947445538 Functional Loss SNV dbSNP153 33..33 33 - - - 32153 RMVar_ID_32153 Human_SNP_ID_282422985 A-to-I Human chr6 - 73432433 73432433 73432433 TCAATGACTGGGAGCGGTGGCTCACACCTGTAATCCAAGCACTTTGGGAGGCCAAGGCGGGTGGG TCAATGACTGGGAGCGGTGGCTCACACCTGTAGTCCAAGCACTTTGGGAGGCCAAGGCGGGTGGG T C CGAS Ensembl:ENSG00000164430 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs529572338 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_362374,RMVar_hsa_circ_333374,RMVar_hsa_circ_352239 32154 RMVar_ID_32154 Human_SNP_ID_282423107 A-to-I Human chr6 - 73432984 73432984 73432984 CACCTCCTGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGTGCCCA CACCTCCTGGGTTCAAGCGATTCTCCTGCCTCGGCCTCCTGAGTAGCTGGGATTACAGGTGCCCA T C CGAS Ensembl:ENSG00000164430 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1419044608 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_362374,RMVar_hsa_circ_333374,RMVar_hsa_circ_352239 32155 RMVar_ID_32155 Human_SNP_ID_282426781 A-to-I Human chr6 - 73448688 73448688 73448688 AGGCGGGAGTTTGAGTCCAGCCTGGACAACATAGTGAGACCCCAGCTCTACCAAAAATAAGTTAA AGGCGGGAGTTTGAGTCCAGCCTGGACAACATTGTGAGACCCCAGCTCTACCAAAAATAAGTTAA T A CGAS Ensembl:ENSG00000164430 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1013110562 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110684,RMVar_hsa_circ_239497 32156 RMVar_ID_32156 Human_SNP_ID_282426782 A-to-I Human chr6 - 73448688 73448688 73448688 AGGCGGGAGTTTGAGTCCAGCCTGGACAACATAGTGAGACCCCAGCTCTACCAAAAATAAGTTAA AGGCGGGAGTTTGAGTCCAGCCTGGACAACATCGTGAGACCCCAGCTCTACCAAAAATAAGTTAA T G CGAS Ensembl:ENSG00000164430 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1013110562 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110684,RMVar_hsa_circ_239497 32157 RMVar_ID_32157 Human_SNP_ID_282428577 A-to-I Human chr6 + 73453988 73453988 73453988 TCGGCTCACTGTAACCTCTGCCTCCCGGATTCAAGCGATTCTCCTGCCTCAGCCTCCGAAGTAGC TCGGCTCACTGTAACCTCTGCCTCCCGGATTCCAGCGATTCTCCTGCCTCAGCCTCCGAAGTAGC A C RF00017-4501 RNACentral:URS000097CADF SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs921547467 Functional Loss SNV dbSNP153 33..33 33 - - - 32158 RMVar_ID_32158 Human_SNP_ID_282428602 A-to-I Human chr6 + 73454090 73454090 73454090 TTTGTATTTTTAGTAGAAAGGAGTTTCACCATATTGGCCAGGCTGGTCTGGGACTCCTTATCTCG TTTGTATTTTTAGTAGAAAGGAGTTTCACCATCTTGGCCAGGCTGGTCTGGGACTCCTTATCTCG A C RF00017-4501 RNACentral:URS000097CADF SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893366391 Functional Loss SNV dbSNP153 33..33 33 - - - 32159 RMVar_ID_32159 Human_SNP_ID_282428709 A-to-I Human chr6 + 73454572 73454572 73454572 ACCCATCTCTACTAAAAATACAAAAATTAGCCAGGTGTGGTGGGCCATGCTTGTAAACCCAGCTA ACCCATCTCTACTAAAAATACAAAAATTAGCCGGGTGTGGTGGGCCATGCTTGTAAACCCAGCTA A G RF00017-4501 RNACentral:URS000097CADF SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs756261458 Functional Loss SNV dbSNP153 33..33 33 - - - 32160 RMVar_ID_32160 Human_SNP_ID_282430116 A-to-I Human chr6 + 73460660 73460660 73460660 GAGCTCAGGCAATCTGCCCCCTTCGGCCTTCCAAAGTGCTAGGATTACAGGCGTGATCCACCATG GAGCTCAGGCAATCTGCCCCCTTCGGCCTTCCCAAGTGCTAGGATTACAGGCGTGATCCACCATG A C RF00017-4501 RNACentral:URS000097CADF SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1423508980 Functional Loss SNV dbSNP153 33..33 33 - - - 32161 RMVar_ID_32161 Human_SNP_ID_282431642 A-to-I Human chr6 + 73465344 73465344 73465344 AACTGCCATGCCTGGCTATTTTTTTGTATTTTAGTAGAGACGGGGTTTCACCGTGTCGCCCAGGG AACTGCCATGCCTGGCTATTTTTTTGTATTTTGGTAGAGACGGGGTTTCACCGTGTCGCCCAGGG A G MTO1 Ensembl:ENSG00000135297 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs571099240 Functional Loss SNV dbSNP153 33..33 33 - - - 32162 RMVar_ID_32162 Human_SNP_ID_282431788 A-to-I Human chr6 + 73465916 73465916 73465916 TGAGGCAGGAGAATCGCTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCCGAGATTGTACCACTGC TGAGGCAGGAGAATCGCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCCGAGATTGTACCACTGC A G MTO1 Ensembl:ENSG00000135297 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1404561302 Functional Loss SNV dbSNP153 33..33 33 - - - 32163 RMVar_ID_32163 Human_SNP_ID_282432412 A-to-I Human chr6 + 73468217 73468217 73468217 TTGGCTCACTGCAACGTTCCCCTCCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGC TTGGCTCACTGCAACGTTCCCCTCCCAGGTTCGAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGC A G MTO1 Ensembl:ENSG00000135297 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1284395374 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6671,RMVar_hsa_circ_304111,RMVar_hsa_circ_11007,RMVar_hsa_circ_14116,RMVar_hsa_circ_69724,RMVar_hsa_circ_239498,RMVar_hsa_circ_18593 32164 RMVar_ID_32164 Human_SNP_ID_282434263 A-to-I Human chr6 + 73475338 73475338 73475338 GAGATTCAGTCTTGTTGCCCAACCTGTGGTGCAATGGCACGATCTCAGCTCACTGCAGCCTCCGC GAGATTCAGTCTTGTTGCCCAACCTGTGGTGCCATGGCACGATCTCAGCTCACTGCAGCCTCCGC A C MTO1 Ensembl:ENSG00000135297 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs998354663 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5655,RMVar_hsa_circ_304111,RMVar_hsa_circ_11007,RMVar_hsa_circ_14116,RMVar_hsa_circ_69724,RMVar_hsa_circ_239498,RMVar_hsa_circ_104798,RMVar_hsa_circ_360194,RMVar_hsa_circ_327495,RMVar_hsa_circ_22240,RMVar_hsa_circ_239500,RMVar_hsa_circ_239501,RMVar_hsa_circ_239502 32165 RMVar_ID_32165 Human_SNP_ID_282434349 A-to-I Human chr6 + 73475654 73475654 73475654 CTCCCGCCTCAGTCTCTTAAGTAGCTGGGATTACAGGCATGTGCCACCACACCTGGCTAATTTTG CTCCCGCCTCAGTCTCTTAAGTAGCTGGGATTCCAGGCATGTGCCACCACACCTGGCTAATTTTG A C MTO1 Ensembl:ENSG00000135297 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1293404674 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5655,RMVar_hsa_circ_304111,RMVar_hsa_circ_11007,RMVar_hsa_circ_14116,RMVar_hsa_circ_69724,RMVar_hsa_circ_239498,RMVar_hsa_circ_104798,RMVar_hsa_circ_360194,RMVar_hsa_circ_327495,RMVar_hsa_circ_22240,RMVar_hsa_circ_239500,RMVar_hsa_circ_239501,RMVar_hsa_circ_239502 32166 RMVar_ID_32166 Human_SNP_ID_282435030 A-to-I Human chr6 + 73478178 73478178 73478178 GGCTGAGGCAGAATTGCTTGAACCCGGGAGGCAGAGGTTGCAGTGAGCAGAGATGATGCCACTGC GGCTGAGGCAGAATTGCTTGAACCCGGGAGGCCGAGGTTGCAGTGAGCAGAGATGATGCCACTGC A C MTO1 Ensembl:ENSG00000135297 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs975144350 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5655,RMVar_hsa_circ_304111,RMVar_hsa_circ_11007,RMVar_hsa_circ_14116,RMVar_hsa_circ_69724,RMVar_hsa_circ_239498,RMVar_hsa_circ_104798,RMVar_hsa_circ_360194,RMVar_hsa_circ_327495,RMVar_hsa_circ_22240,RMVar_hsa_circ_239500,RMVar_hsa_circ_239501,RMVar_hsa_circ_239502 32167 RMVar_ID_32167 Human_SNP_ID_282435180 A-to-I Human chr6 + 73478762 73478761 73478762 CAGAGTTTTACCATGTTGACCAGGCTGTTCTCAAACTCCTGACCTCAGGTGATCCACACACCTTG CAGAGTTTTACCATGTTGACCAGGCTGTTCTC_AACTCCTGACCTCAGGTGATCCACACACCTTG CA C MTO1 Ensembl:ENSG00000135297 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1055023708 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_5655,RMVar_hsa_circ_304111,RMVar_hsa_circ_11007,RMVar_hsa_circ_14116,RMVar_hsa_circ_69724,RMVar_hsa_circ_239498,RMVar_hsa_circ_104798,RMVar_hsa_circ_360194,RMVar_hsa_circ_327495,RMVar_hsa_circ_22240,RMVar_hsa_circ_239500,RMVar_hsa_circ_239501,RMVar_hsa_circ_239502 32168 RMVar_ID_32168 Human_SNP_ID_282435184 A-to-I Human chr6 + 73478789 73478789 73478789 TTCTCAAACTCCTGACCTCAGGTGATCCACACACCTTGGCCTCCCAAAGTGCTGGGATTACAGGC TTCTCAAACTCCTGACCTCAGGTGATCCACACCCCTTGGCCTCCCAAAGTGCTGGGATTACAGGC A C MTO1 Ensembl:ENSG00000135297 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs9293931 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_3583,GWAS_ID_3584,GWAS_ID_3585,GWAS_ID_3586,GWAS_ID_3587,GWAS_ID_3588,GWAS_ID_3589,GWAS_ID_3590,GWAS_ID_3591,GWAS_ID_3592,GWAS_ID_3593,GWAS_ID_3594,GWAS_ID_3595,GWAS_ID_3596,GWAS_ID_3597,GWAS_ID_3598,GWAS_ID_3599,GWAS_ID_3600,GWAS_ID_3601,GWAS_ID_3602,GWAS_ID_3603,GWAS_ID_3604,GWAS_ID_3605,GWAS_ID_3606,GWAS_ID_3607,GWAS_ID_3608,GWAS_ID_3609,GWAS_ID_3610,GWAS_ID_3611,GWAS_ID_3612,GWAS_ID_3613,GWAS_ID_3614,GWAS_ID_3615,GWAS_ID_3616,GWAS_ID_3617 RMVar_hsa_circ_5655,RMVar_hsa_circ_304111,RMVar_hsa_circ_11007,RMVar_hsa_circ_14116,RMVar_hsa_circ_69724,RMVar_hsa_circ_239498,RMVar_hsa_circ_104798,RMVar_hsa_circ_360194,RMVar_hsa_circ_327495,RMVar_hsa_circ_22240,RMVar_hsa_circ_239500,RMVar_hsa_circ_239501,RMVar_hsa_circ_239502 32169 RMVar_ID_32169 Human_SNP_ID_282435185 A-to-I Human chr6 + 73478789 73478789 73478789 TTCTCAAACTCCTGACCTCAGGTGATCCACACACCTTGGCCTCCCAAAGTGCTGGGATTACAGGC TTCTCAAACTCCTGACCTCAGGTGATCCACACGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGC A G MTO1 Ensembl:ENSG00000135297 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs9293931 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_3583,GWAS_ID_3584,GWAS_ID_3585,GWAS_ID_3586,GWAS_ID_3587,GWAS_ID_3588,GWAS_ID_3589,GWAS_ID_3590,GWAS_ID_3591,GWAS_ID_3592,GWAS_ID_3593,GWAS_ID_3594,GWAS_ID_3595,GWAS_ID_3596,GWAS_ID_3597,GWAS_ID_3598,GWAS_ID_3599,GWAS_ID_3600,GWAS_ID_3601,GWAS_ID_3602,GWAS_ID_3603,GWAS_ID_3604,GWAS_ID_3605,GWAS_ID_3606,GWAS_ID_3607,GWAS_ID_3608,GWAS_ID_3609,GWAS_ID_3610,GWAS_ID_3611,GWAS_ID_3612,GWAS_ID_3613,GWAS_ID_3614,GWAS_ID_3615,GWAS_ID_3616,GWAS_ID_3617 RMVar_hsa_circ_5655,RMVar_hsa_circ_304111,RMVar_hsa_circ_11007,RMVar_hsa_circ_14116,RMVar_hsa_circ_69724,RMVar_hsa_circ_239498,RMVar_hsa_circ_104798,RMVar_hsa_circ_360194,RMVar_hsa_circ_327495,RMVar_hsa_circ_22240,RMVar_hsa_circ_239500,RMVar_hsa_circ_239501,RMVar_hsa_circ_239502 32170 RMVar_ID_32170 Human_SNP_ID_282435186 A-to-I Human chr6 + 73478789 73478789 73478789 TTCTCAAACTCCTGACCTCAGGTGATCCACACACCTTGGCCTCCCAAAGTGCTGGGATTACAGGC TTCTCAAACTCCTGACCTCAGGTGATCCACACTCCTTGGCCTCCCAAAGTGCTGGGATTACAGGC A T MTO1 Ensembl:ENSG00000135297 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs9293931 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_3583,GWAS_ID_3584,GWAS_ID_3585,GWAS_ID_3586,GWAS_ID_3587,GWAS_ID_3588,GWAS_ID_3589,GWAS_ID_3590,GWAS_ID_3591,GWAS_ID_3592,GWAS_ID_3593,GWAS_ID_3594,GWAS_ID_3595,GWAS_ID_3596,GWAS_ID_3597,GWAS_ID_3598,GWAS_ID_3599,GWAS_ID_3600,GWAS_ID_3601,GWAS_ID_3602,GWAS_ID_3603,GWAS_ID_3604,GWAS_ID_3605,GWAS_ID_3606,GWAS_ID_3607,GWAS_ID_3608,GWAS_ID_3609,GWAS_ID_3610,GWAS_ID_3611,GWAS_ID_3612,GWAS_ID_3613,GWAS_ID_3614,GWAS_ID_3615,GWAS_ID_3616,GWAS_ID_3617 RMVar_hsa_circ_5655,RMVar_hsa_circ_304111,RMVar_hsa_circ_11007,RMVar_hsa_circ_14116,RMVar_hsa_circ_69724,RMVar_hsa_circ_239498,RMVar_hsa_circ_104798,RMVar_hsa_circ_360194,RMVar_hsa_circ_327495,RMVar_hsa_circ_22240,RMVar_hsa_circ_239500,RMVar_hsa_circ_239501,RMVar_hsa_circ_239502 32171 RMVar_ID_32171 Human_SNP_ID_282436953 A-to-I Human chr6 + 73484932 73484932 73484932 AGCCAGGCATGGTGGAGCACACCTGTAATCCCAGCTATTCAAGAGGCTGAGGGAGGAGAATCACT AGCCAGGCATGGTGGAGCACACCTGTAATCCCTGCTATTCAAGAGGCTGAGGGAGGAGAATCACT A T MTO1 Ensembl:ENSG00000135297 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs565518799 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7565,RMVar_hsa_circ_69724,RMVar_hsa_circ_239507,RMVar_hsa_circ_326113,RMVar_hsa_circ_332706,RMVar_hsa_circ_239508,RMVar_hsa_circ_2147,RMVar_hsa_circ_301020,RMVar_hsa_circ_70169,RMVar_hsa_circ_239511,RMVar_hsa_circ_346379,RMVar_hsa_circ_368868,RMVar_hsa_circ_324832,RMVar_hsa_circ_239510 32172 RMVar_ID_32172 Human_SNP_ID_282436958 A-to-I Human chr6 + 73484940 73484940 73484940 ATGGTGGAGCACACCTGTAATCCCAGCTATTCAAGAGGCTGAGGGAGGAGAATCACTTGAACCTA ATGGTGGAGCACACCTGTAATCCCAGCTATTCGAGAGGCTGAGGGAGGAGAATCACTTGAACCTA A G MTO1 Ensembl:ENSG00000135297 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs528170263 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7565,RMVar_hsa_circ_69724,RMVar_hsa_circ_239507,RMVar_hsa_circ_326113,RMVar_hsa_circ_332706,RMVar_hsa_circ_239508,RMVar_hsa_circ_2147,RMVar_hsa_circ_301020,RMVar_hsa_circ_70169,RMVar_hsa_circ_239511,RMVar_hsa_circ_346379,RMVar_hsa_circ_368868,RMVar_hsa_circ_324832,RMVar_hsa_circ_239510 32173 RMVar_ID_32173 Human_SNP_ID_282437824 A-to-I Human chr6 + 73488307 73488307 73488307 GTGATCCTCCCACCTCAGCCTCCCAAGTAGCTAGGACCACAGGTGCACACCACCACATCCAGCTA GTGATCCTCCCACCTCAGCCTCCCAAGTAGCTGGGACCACAGGTGCACACCACCACATCCAGCTA A G MTO1 Ensembl:ENSG00000135297 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1422801792 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7565,RMVar_hsa_circ_69724,RMVar_hsa_circ_239507,RMVar_hsa_circ_326113,RMVar_hsa_circ_332706,RMVar_hsa_circ_239508,RMVar_hsa_circ_2147,RMVar_hsa_circ_301020,RMVar_hsa_circ_70169,RMVar_hsa_circ_239511,RMVar_hsa_circ_346379,RMVar_hsa_circ_324832,RMVar_hsa_circ_239510 32174 RMVar_ID_32174 Human_SNP_ID_282437825 A-to-I Human chr6 + 73488307 73488307 73488307 GTGATCCTCCCACCTCAGCCTCCCAAGTAGCTAGGACCACAGGTGCACACCACCACATCCAGCTA GTGATCCTCCCACCTCAGCCTCCCAAGTAGCTTGGACCACAGGTGCACACCACCACATCCAGCTA A T MTO1 Ensembl:ENSG00000135297 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1422801792 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7565,RMVar_hsa_circ_69724,RMVar_hsa_circ_239507,RMVar_hsa_circ_326113,RMVar_hsa_circ_332706,RMVar_hsa_circ_239508,RMVar_hsa_circ_2147,RMVar_hsa_circ_301020,RMVar_hsa_circ_70169,RMVar_hsa_circ_239511,RMVar_hsa_circ_346379,RMVar_hsa_circ_324832,RMVar_hsa_circ_239510 32175 RMVar_ID_32175 Human_SNP_ID_282440252 A-to-I Human chr6 + 73497326 73497326 73497326 AGGTGGATGCCACCACGCCTGGCTAATTTTTTATATTTTTAGTAGAGATGGCATTTCACCATGTT AGGTGGATGCCACCACGCCTGGCTAATTTTTTGTATTTTTAGTAGAGATGGCATTTCACCATGTT A G MTO1 Ensembl:ENSG00000135297 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs927290305 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15875263 RMVar_hsa_circ_332706,RMVar_hsa_circ_239508,RMVar_hsa_circ_2147,RMVar_hsa_circ_70169,RMVar_hsa_circ_346379,RMVar_hsa_circ_239510,RMVar_hsa_circ_358723 32176 RMVar_ID_32176 Human_SNP_ID_282440253 A-to-I Human chr6 + 73497334 73497333 73497334 GCCACCACGCCTGGCTAATTTTTTATATTTTTAGTAGAGATGGCATTTCACCATGTTCCCCATGC GCCACCACGCCTGGCTAATTTTTTATATTTTT_GTAGAGATGGCATTTCACCATGTTCCCCATGC TA T MTO1 Ensembl:ENSG00000135297 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs958712470 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_332706,RMVar_hsa_circ_239508,RMVar_hsa_circ_2147,RMVar_hsa_circ_70169,RMVar_hsa_circ_346379,RMVar_hsa_circ_239510,RMVar_hsa_circ_358723 32177 RMVar_ID_32177 Human_SNP_ID_282440272 A-to-I Human chr6 + 73497422 73497420 73497423 ACTATCCACCCGCCTTGGCCTCCCAAAGTGTTAGTATTACAGGCATGAGCCACCATGCCTGGCCA ACTATCCACCCGCCTTGGCCTCCCAAAGTGT___TATTACAGGCATGAGCCACCATGCCTGGCCA TTAG T MTO1 Ensembl:ENSG00000135297 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1473753401 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_332706,RMVar_hsa_circ_239508,RMVar_hsa_circ_2147,RMVar_hsa_circ_70169,RMVar_hsa_circ_346379,RMVar_hsa_circ_239510,RMVar_hsa_circ_358723 32178 RMVar_ID_32178 Human_SNP_ID_282445192 A-to-I Human chr6 - 73516444 73516444 73516444 TTACAGGCATGTGCTAATTTGGTGTTTTTAATAGAGATGAGGTTTTTCCATGTTGGTCAGGCTGG TTACAGGCATGTGCTAATTTGGTGTTTTTAATGGAGATGAGGTTTTTCCATGTTGGTCAGGCTGG T C EEF1A1 Ensembl:ENSG00000156508 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900352907 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_667877,Human_RBP_ID_3814621,Human_RBP_ID_7627164,Human_RBP_ID_8903190,Human_RBP_ID_10296617,Human_RBP_ID_15875556,Human_RBP_ID_18080457,Human_RBP_ID_24171112,Human_RBP_ID_27758272 RMVar_hsa_circ_98369,RMVar_hsa_circ_119060,RMVar_hsa_circ_102380,RMVar_hsa_circ_239513,RMVar_hsa_circ_239515,RMVar_hsa_circ_93670,RMVar_hsa_circ_239514,RMVar_hsa_circ_239512 32179 RMVar_ID_32179 Human_SNP_ID_282445205 A-to-I Human chr6 - 73516501 73516501 73516501 ATCTCCTCCTCCTGGGTTCAAGCAATTCTCCTACTTCAGCCTCCCAAGTAGCTGGGATTACAGGC ATCTCCTCCTCCTGGGTTCAAGCAATTCTCCTTCTTCAGCCTCCCAAGTAGCTGGGATTACAGGC T A EEF1A1 Ensembl:ENSG00000156508 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1036911111 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_667879,Human_RBP_ID_9198279,Human_RBP_ID_17307949,Human_RBP_ID_17420799 RMVar_hsa_circ_98369,RMVar_hsa_circ_119060,RMVar_hsa_circ_102380,RMVar_hsa_circ_239513,RMVar_hsa_circ_239515,RMVar_hsa_circ_93670,RMVar_hsa_circ_239514,RMVar_hsa_circ_239512 32180 RMVar_ID_32180 Human_SNP_ID_282445206 A-to-I Human chr6 - 73516501 73516501 73516501 ATCTCCTCCTCCTGGGTTCAAGCAATTCTCCTACTTCAGCCTCCCAAGTAGCTGGGATTACAGGC ATCTCCTCCTCCTGGGTTCAAGCAATTCTCCTGCTTCAGCCTCCCAAGTAGCTGGGATTACAGGC T C EEF1A1 Ensembl:ENSG00000156508 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1036911111 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_667879,Human_RBP_ID_9198279,Human_RBP_ID_17307949,Human_RBP_ID_17420799 RMVar_hsa_circ_98369,RMVar_hsa_circ_119060,RMVar_hsa_circ_102380,RMVar_hsa_circ_239513,RMVar_hsa_circ_239515,RMVar_hsa_circ_93670,RMVar_hsa_circ_239514,RMVar_hsa_circ_239512 32181 RMVar_ID_32181 Human_SNP_ID_282445229 A-to-I Human chr6 - 73516560 73516560 73516560 TTTTTTAAGATGGAGTTCTTGTTGCCCAGGCTAGAATGCAATGGCAAAATCTCACTGCAATCTCC TTTTTTAAGATGGAGTTCTTGTTGCCCAGGCTGGAATGCAATGGCAAAATCTCACTGCAATCTCC T C EEF1A1 Ensembl:ENSG00000156508 Protein coding 3'UTR GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1243272987 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_667879,Human_RBP_ID_1048548,Human_RBP_ID_1675893,Human_RBP_ID_3017300,Human_RBP_ID_7627168,Human_RBP_ID_8903194,Human_RBP_ID_9198280,Human_RBP_ID_9308735,Human_RBP_ID_15875566,Human_RBP_ID_17420801,Human_RBP_ID_18373376,Human_RBP_ID_18869069,Human_RBP_ID_24171113,Human_RBP_ID_27758275 Human_miRNA_ID_981562,Human_miRNA_ID_986285 RMVar_hsa_circ_98369,RMVar_hsa_circ_119060,RMVar_hsa_circ_102380,RMVar_hsa_circ_239513,RMVar_hsa_circ_239515,RMVar_hsa_circ_93670,RMVar_hsa_circ_239514,RMVar_hsa_circ_239512 32182 RMVar_ID_32182 Human_SNP_ID_282449587 A-to-I Human chr6 + 73530161 73530161 73530161 CGTCTGCCTCAGCCTCCCAAAGTGCTGGGATTATAGACGTGAGCCACCACACCAGCCTATTCTAT CGTCTGCCTCAGCCTCCCAAAGTGCTGGGATTGTAGACGTGAGCCACCACACCAGCCTATTCTAT A G AL121972.1 Ensembl:ENSG00000229862 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1309325633 Functional Loss SNV dbSNP153 33..33 33 - - - 32183 RMVar_ID_32183 Human_SNP_ID_282465757 A-to-I Human chr6 - 73593820 73593820 73593820 CTTCAAGCGATCCTCCTGTCTCGGCCTCACAAAGTGTTGAGACTACAGGCATGAGCCACTGTGCC CTTCAAGCGATCCTCCTGTCTCGGCCTCACAATGTGTTGAGACTACAGGCATGAGCCACTGTGCC T A SLC17A5 Ensembl:ENSG00000119899 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1338817523 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_667938 RMVar_hsa_circ_102225,RMVar_hsa_circ_239539 32184 RMVar_ID_32184 Human_SNP_ID_282465884 A-to-I Human chr6 - 73594290 73594290 73594290 GAAGCGGCCGGGCACGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGGGGCTGAGGTGGGCGAA GAAGCGGCCGGGCACGGTGGCTCATGCCTGTAGTCCCAGCACTTTGGGGGGCTGAGGTGGGCGAA T C SLC17A5 Ensembl:ENSG00000119899 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1133168 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1941881,Human_miRNA_ID_1944925,Human_miRNA_ID_2116072,Human_miRNA_ID_2199645,Human_miRNA_ID_2202712,Human_miRNA_ID_2315138,Human_miRNA_ID_2318298,Human_miRNA_ID_2321455,Human_miRNA_ID_2324613,Human_miRNA_ID_2327754,Human_miRNA_ID_2518993,Human_miRNA_ID_2522163,Human_miRNA_ID_2774007,Human_miRNA_ID_2815174,Human_miRNA_ID_2821358,Human_miRNA_ID_2827489,Human_miRNA_ID_2830640,Human_miRNA_ID_2834759,Human_miRNA_ID_2840122,Human_miRNA_ID_2845282,Human_miRNA_ID_2848304,Human_miRNA_ID_2862437,Human_miRNA_ID_3112164 RMVar_hsa_circ_102225,RMVar_hsa_circ_239539 32185 RMVar_ID_32185 Human_SNP_ID_282479349 A-to-I Human chr6 - 73646796 73646796 73646796 TGCTGCCATATGCCTTTAGTCCCAGCTACTCAAGAGGCTGAGGTGAGAGGATCACTTGAGTCCAG TGCTGCCATATGCCTTTAGTCCCAGCTACTCAGGAGGCTGAGGTGAGAGGATCACTTGAGTCCAG T C SLC17A5 Ensembl:ENSG00000119899 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs919883300 Functional Loss SNV dbSNP153 33..33 33 - - - 32186 RMVar_ID_32186 Human_SNP_ID_282479363 A-to-I Human chr6 - 73646837 73646837 73646837 ACCCCGACTCTACAAGTAAAAATTTAAAAATTAGTCAGATATGCTGCCATATGCCTTTAGTCCCA ACCCCGACTCTACAAGTAAAAATTTAAAAATTTGTCAGATATGCTGCCATATGCCTTTAGTCCCA T A SLC17A5 Ensembl:ENSG00000119899 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1482436162 Functional Loss SNV dbSNP153 33..33 33 - - - 32187 RMVar_ID_32187 Human_SNP_ID_282481105 A-to-I Human chr6 - 73653843 73653843 73653843 GGTTCGAGACCTGGCCCGGAACGATGGCGAGGAGAGCACGGACCGCACGCCTCTTCTACCGGGCG GGTTCGAGACCTGGCCCGGAACGATGGCGAGGGGAGCACGGACCGCACGCCTCTTCTACCGGGCG T C SLC17A5 Ensembl:ENSG00000119899 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs201942170 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4897045 Human_Splice_Rec_786837 32188 RMVar_ID_32188 Human_SNP_ID_282481106 A-to-I Human chr6 - 73653843 73653843 73653843 GGTTCGAGACCTGGCCCGGAACGATGGCGAGGAGAGCACGGACCGCACGCCTCTTCTACCGGGCG GGTTCGAGACCTGGCCCGGAACGATGGCGAGGCGAGCACGGACCGCACGCCTCTTCTACCGGGCG T G SLC17A5 Ensembl:ENSG00000119899 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs201942170 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4897045 Human_Splice_Rec_786837 32189 RMVar_ID_32189 Human_SNP_ID_503745521 A-to-I Human chr12 - 61666768 61666768 61666768 CACATGAAGAAATCTAGAAGAGACTTCTAACAACCCTGAAATACCTAGAAGAAAATAGAAAAAGA CACATGAAGAAATCTAGAAGAGACTTCTAACAGCCCTGAAATACCTAGAAGAAAATAGAAAAAGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs7139073 Functional Loss SNV dbSNP153 33..33 33 - - - 32190 RMVar_ID_32190 Human_SNP_ID_503745522 A-to-I Human chr12 - 61666768 61666768 61666768 CACATGAAGAAATCTAGAAGAGACTTCTAACAACCCTGAAATACCTAGAAGAAAATAGAAAAAGA CACATGAAGAAATCTAGAAGAGACTTCTAACACCCCTGAAATACCTAGAAGAAAATAGAAAAAGA T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs7139073 Functional Loss SNV dbSNP153 33..33 33 - - - 32191 RMVar_ID_32191 Human_SNP_ID_503745525 A-to-I Human chr12 - 61666771 61666771 61666771 TACCACATGAAGAAATCTAGAAGAGACTTCTAACAACCCTGAAATACCTAGAAGAAAATAGAAAA TACCACATGAAGAAATCTAGAAGAGACTTCTAGCAACCCTGAAATACCTAGAAGAAAATAGAAAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs979980720 Functional Loss SNV dbSNP153 33..33 33 - - - 32192 RMVar_ID_32192 Human_SNP_ID_503760131 A-to-I Human chr12 - 61725898 61725898 61725898 CACCAACCCTTCTCCCCAAATCCCCAAAGTTTATTGTATCATTCTTATGCCTTTGTGTCTGCATA CACCAACCCTTCTCCCCAAATCCCCAAAGTTTGTTGTATCATTCTTATGCCTTTGTGTCTGCATA T C TAFA2 Ensembl:ENSG00000198673 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs111288713 Functional Loss SNV dbSNP153 33..33 33 - - - 32193 RMVar_ID_32193 Human_SNP_ID_503889886 A-to-I Human chr12 + 62265616 62265616 62265616 TCACCCAGGCTGGAGTGTAGTGGCATAGTCATAGCTCACTGTAGCTTCAAACTCCTTGGCTCAAG TCACCCAGGCTGGAGTGTAGTGGCATAGTCATCGCTCACTGTAGCTTCAAACTCCTTGGCTCAAG A C USP15 Ensembl:ENSG00000135655 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1258708083 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11998545 RMVar_hsa_circ_117655,RMVar_hsa_circ_157789 32194 RMVar_ID_32194 Human_SNP_ID_503894783 A-to-I Human chr12 + 62286175 62286175 62286175 CATACAACAAAAGACTAATATCTGGACTCTATAAGGAACTTAATAAGAAAAAAAACGCCCATTAA CATACAACAAAAGACTAATATCTGGACTCTATGAGGAACTTAATAAGAAAAAAAACGCCCATTAA A G USP15 Ensembl:ENSG00000135655 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1324426585 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117655,RMVar_hsa_circ_157789 32195 RMVar_ID_32195 Human_SNP_ID_503894854 A-to-I Human chr12 + 62286486 62286486 62286486 AAGAAAGCAGTTTGGAGATTTCTCAAAGAACTAAAAATAGAAATACCATTCGCTCAGCAGTCCCA AAGAAAGCAGTTTGGAGATTTCTCAAAGAACTGAAAATAGAAATACCATTCGCTCAGCAGTCCCA A G USP15 Ensembl:ENSG00000135655 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1476068542 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117655,RMVar_hsa_circ_157789 32196 RMVar_ID_32196 Human_SNP_ID_503894856 A-to-I Human chr12 + 62286492 62286492 62286492 GCAGTTTGGAGATTTCTCAAAGAACTAAAAATAGAAATACCATTCGCTCAGCAGTCCCATTACTA GCAGTTTGGAGATTTCTCAAAGAACTAAAAATGGAAATACCATTCGCTCAGCAGTCCCATTACTA A G USP15 Ensembl:ENSG00000135655 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs563850751 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117655,RMVar_hsa_circ_157789 32197 RMVar_ID_32197 Human_SNP_ID_503894882 A-to-I Human chr12 + 62286562 62286561 62286563 TAAATCATTCTACCAAAAAGACACTTACACTCATATGTTTATCACAGTACTGTTCACAATAGTAA TAAATCATTCTACCAAAAAGACACTTACACTC__ATGTTTATCACAGTACTGTTCACAATAGTAA CAT C USP15 Ensembl:ENSG00000135655 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1354494887 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_117655,RMVar_hsa_circ_157789 32198 RMVar_ID_32198 Human_SNP_ID_503902612 A-to-I Human chr12 + 62319093 62319093 62319093 GTTTAATTGACTTACAGTTCCATAGGCCGTACAGGAAGCATGGCTAGAAGGCCTCAGGAAACTTA GTTTAATTGACTTACAGTTCCATAGGCCGTACGGGAAGCATGGCTAGAAGGCCTCAGGAAACTTA A G USP15 Ensembl:ENSG00000135655 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1378790953 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45065,RMVar_hsa_circ_117655,RMVar_hsa_circ_157789,RMVar_hsa_circ_324751,RMVar_hsa_circ_330868,RMVar_hsa_circ_333336,RMVar_hsa_circ_93458,RMVar_hsa_circ_157791,RMVar_hsa_circ_157792,RMVar_hsa_circ_111411,RMVar_hsa_circ_365386,RMVar_hsa_circ_157793,RMVar_hsa_circ_157794,RMVar_hsa_circ_273103,RMVar_hsa_circ_302607,RMVar_hsa_circ_322273,RMVar_hsa_circ_157795 32199 RMVar_ID_32199 Human_SNP_ID_503919173 A-to-I Human chr12 + 62388982 62388982 62388982 GAGACCTTGTCTCTAAAAAATAAAAATTAGCCAGTCATGGTGTCACACGCATGTAGTCCTAGCTA GAGACCTTGTCTCTAAAAAATAAAAATTAGCCCGTCATGGTGTCACACGCATGTAGTCCTAGCTA A C USP15 Ensembl:ENSG00000135655 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1044327465 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45065,RMVar_hsa_circ_24145,RMVar_hsa_circ_63010,RMVar_hsa_circ_55629,RMVar_hsa_circ_72280,RMVar_hsa_circ_51855,RMVar_hsa_circ_363795,RMVar_hsa_circ_11498,RMVar_hsa_circ_37545,RMVar_hsa_circ_56383,RMVar_hsa_circ_309361,RMVar_hsa_circ_54198,RMVar_hsa_circ_31240 32200 RMVar_ID_32200 Human_SNP_ID_503919174 A-to-I Human chr12 + 62388982 62388982 62388982 GAGACCTTGTCTCTAAAAAATAAAAATTAGCCAGTCATGGTGTCACACGCATGTAGTCCTAGCTA GAGACCTTGTCTCTAAAAAATAAAAATTAGCCGGTCATGGTGTCACACGCATGTAGTCCTAGCTA A G USP15 Ensembl:ENSG00000135655 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1044327465 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45065,RMVar_hsa_circ_24145,RMVar_hsa_circ_63010,RMVar_hsa_circ_55629,RMVar_hsa_circ_72280,RMVar_hsa_circ_51855,RMVar_hsa_circ_363795,RMVar_hsa_circ_11498,RMVar_hsa_circ_37545,RMVar_hsa_circ_56383,RMVar_hsa_circ_309361,RMVar_hsa_circ_54198,RMVar_hsa_circ_31240 32201 RMVar_ID_32201 Human_SNP_ID_503921395 A-to-I Human chr12 + 62397772 62397772 62397772 CCAGCCACTCGGGAGGCTGAGGTAGGAGAATCACTTGAACCAGGGAGCCGGAGGTTGCAGAGAGC CCAGCCACTCGGGAGGCTGAGGTAGGAGAATCGCTTGAACCAGGGAGCCGGAGGTTGCAGAGAGC A G USP15 Ensembl:ENSG00000135655 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1176707789 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51855,RMVar_hsa_circ_37545,RMVar_hsa_circ_366258 32202 RMVar_ID_32202 Human_SNP_ID_503921493 A-to-I Human chr12 + 62398138 62398138 62398138 CTTTGCCTCCCGAGTAGCTGGACTACAGGCACATGCCACCACACCCAGCTAATTTTTTTGTATTT CTTTGCCTCCCGAGTAGCTGGACTACAGGCACGTGCCACCACACCCAGCTAATTTTTTTGTATTT A G USP15 Ensembl:ENSG00000135655 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs370193975 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51855,RMVar_hsa_circ_37545,RMVar_hsa_circ_366258 32203 RMVar_ID_32203 Human_SNP_ID_503921506 A-to-I Human chr12 + 62398173 62398173 62398173 CCACCACACCCAGCTAATTTTTTTGTATTTTTAGTAGCAGTGGGGTTTCACCATGGTGCCCAGGC CCACCACACCCAGCTAATTTTTTTGTATTTTTGGTAGCAGTGGGGTTTCACCATGGTGCCCAGGC A G USP15 Ensembl:ENSG00000135655 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1055140711 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51855,RMVar_hsa_circ_37545,RMVar_hsa_circ_366258 32204 RMVar_ID_32204 Human_SNP_ID_503940931 A-to-I Human chr12 + 62476900 62476900 62476900 AGAGCAGGGGTTAGGTGTGGAAGCTTATGCATATAATCCTGGGACTTTGGGAGGCGAAGACTGGA AGAGCAGGGGTTAGGTGTGGAAGCTTATGCATGTAATCCTGGGACTTTGGGAGGCGAAGACTGGA A G MON2 Ensembl:ENSG00000061987 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1471652075 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6205516,Human_RBP_ID_22574802 RMVar_hsa_circ_157805,RMVar_hsa_circ_280472,RMVar_hsa_circ_291413,RMVar_hsa_circ_339216,RMVar_hsa_circ_354745,RMVar_hsa_circ_291495,RMVar_hsa_circ_287677,RMVar_hsa_circ_28740,RMVar_hsa_circ_64104,RMVar_hsa_circ_157806,RMVar_hsa_circ_157807,RMVar_hsa_circ_157804 32205 RMVar_ID_32205 Human_SNP_ID_503944443 A-to-I Human chr12 + 62492973 62492973 62492973 TGCTCTCCAGCCTGGGGACAGAACAAGATTCCATCTCAGAAAAACAAAACAAAAAAAACCAAAAA TGCTCTCCAGCCTGGGGACAGAACAAGATTCCTTCTCAGAAAAACAAAACAAAAAAAACCAAAAA A T MON2 Ensembl:ENSG00000061987 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1032794810 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95869,RMVar_hsa_circ_157805,RMVar_hsa_circ_280472,RMVar_hsa_circ_291413,RMVar_hsa_circ_339216,RMVar_hsa_circ_354745,RMVar_hsa_circ_291495,RMVar_hsa_circ_287677,RMVar_hsa_circ_28740,RMVar_hsa_circ_64104,RMVar_hsa_circ_157806,RMVar_hsa_circ_157807,RMVar_hsa_circ_157808,RMVar_hsa_circ_157804,RMVar_hsa_circ_285627,RMVar_hsa_circ_317939,RMVar_hsa_circ_335450,RMVar_hsa_circ_293378,RMVar_hsa_circ_276127,RMVar_hsa_circ_58858,RMVar_hsa_circ_157811,RMVar_hsa_circ_157813,RMVar_hsa_circ_157814,RMVar_hsa_circ_157812,RMVar_hsa_circ_157810,RMVar_hsa_circ_157816,RMVar_hsa_circ_157815 32206 RMVar_ID_32206 Human_SNP_ID_503947903 A-to-I Human chr12 + 62507808 62507808 62507808 TATGATTATTTGAGACAGCATCTTGCTCTGTTACCCAGACTGGAGGGCAGTGGCATGATCACGGC TATGATTATTTGAGACAGCATCTTGCTCTGTTGCCCAGACTGGAGGGCAGTGGCATGATCACGGC A G MON2 Ensembl:ENSG00000061987 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1258977895 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12000508 RMVar_hsa_circ_18305,RMVar_hsa_circ_95869,RMVar_hsa_circ_291413,RMVar_hsa_circ_354745,RMVar_hsa_circ_291495,RMVar_hsa_circ_28740,RMVar_hsa_circ_64104,RMVar_hsa_circ_157806,RMVar_hsa_circ_157807,RMVar_hsa_circ_335450,RMVar_hsa_circ_293378,RMVar_hsa_circ_58858,RMVar_hsa_circ_157813,RMVar_hsa_circ_157814,RMVar_hsa_circ_32411,RMVar_hsa_circ_157815,RMVar_hsa_circ_344029,RMVar_hsa_circ_51539,RMVar_hsa_circ_287007,RMVar_hsa_circ_47350,RMVar_hsa_circ_157820,RMVar_hsa_circ_305543,RMVar_hsa_circ_157818,RMVar_hsa_circ_360174,RMVar_hsa_circ_35696,RMVar_hsa_circ_330090,RMVar_hsa_circ_54301,RMVar_hsa_circ_157821,RMVar_hsa_circ_81252,RMVar_hsa_circ_290573,RMVar_hsa_circ_357269,RMVar_hsa_circ_59746,RMVar_hsa_circ_36819,RMVar_hsa_circ_157822,RMVar_hsa_circ_157823 32207 RMVar_ID_32207 Human_SNP_ID_503947912 A-to-I Human chr12 + 62507842 62507842 62507842 CCAGACTGGAGGGCAGTGGCATGATCACGGCTAACTGCAGCCTTGACCTCCTGGGTTCAAGTGTT CCAGACTGGAGGGCAGTGGCATGATCACGGCTCACTGCAGCCTTGACCTCCTGGGTTCAAGTGTT A C MON2 Ensembl:ENSG00000061987 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1398960713 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18305,RMVar_hsa_circ_95869,RMVar_hsa_circ_291413,RMVar_hsa_circ_354745,RMVar_hsa_circ_291495,RMVar_hsa_circ_28740,RMVar_hsa_circ_64104,RMVar_hsa_circ_157806,RMVar_hsa_circ_157807,RMVar_hsa_circ_335450,RMVar_hsa_circ_293378,RMVar_hsa_circ_58858,RMVar_hsa_circ_157813,RMVar_hsa_circ_157814,RMVar_hsa_circ_32411,RMVar_hsa_circ_157815,RMVar_hsa_circ_344029,RMVar_hsa_circ_51539,RMVar_hsa_circ_287007,RMVar_hsa_circ_47350,RMVar_hsa_circ_157820,RMVar_hsa_circ_305543,RMVar_hsa_circ_157818,RMVar_hsa_circ_360174,RMVar_hsa_circ_35696,RMVar_hsa_circ_330090,RMVar_hsa_circ_54301,RMVar_hsa_circ_157821,RMVar_hsa_circ_81252,RMVar_hsa_circ_290573,RMVar_hsa_circ_357269,RMVar_hsa_circ_59746,RMVar_hsa_circ_36819,RMVar_hsa_circ_157822,RMVar_hsa_circ_157823 32208 RMVar_ID_32208 Human_SNP_ID_503950273 A-to-I Human chr12 + 62518204 62518204 62518204 TCCCATTCATGAGGGTTTCAGCCTTATAACCTAATTTCCTCCGAAAGACTCCACCTTCAAATATC TCCCATTCATGAGGGTTTCAGCCTTATAACCTGATTTCCTCCGAAAGACTCCACCTTCAAATATC A G MON2 Ensembl:ENSG00000061987 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,frontal_cortex - 29129909,30559470 RNA-Seq:(High) rs190640421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17561452 RMVar_hsa_circ_18305,RMVar_hsa_circ_95869,RMVar_hsa_circ_291413,RMVar_hsa_circ_354745,RMVar_hsa_circ_28740,RMVar_hsa_circ_64104,RMVar_hsa_circ_157807,RMVar_hsa_circ_293378,RMVar_hsa_circ_58858,RMVar_hsa_circ_157813,RMVar_hsa_circ_157814,RMVar_hsa_circ_32411,RMVar_hsa_circ_344029,RMVar_hsa_circ_51539,RMVar_hsa_circ_47350,RMVar_hsa_circ_157818,RMVar_hsa_circ_360174,RMVar_hsa_circ_330090,RMVar_hsa_circ_54301,RMVar_hsa_circ_157821,RMVar_hsa_circ_81252,RMVar_hsa_circ_357269,RMVar_hsa_circ_59746,RMVar_hsa_circ_36819,RMVar_hsa_circ_157823,RMVar_hsa_circ_361599,RMVar_hsa_circ_157825 32209 RMVar_ID_32209 Human_SNP_ID_503950279 A-to-I Human chr12 + 62518231 62518231 62518231 AACCTAATTTCCTCCGAAAGACTCCACCTTCAAATATCATCCCACTGGGGAATAGGCTTCAACAC AACCTAATTTCCTCCGAAAGACTCCACCTTCAGATATCATCCCACTGGGGAATAGGCTTCAACAC A G MON2 Ensembl:ENSG00000061987 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1267112298 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18305,RMVar_hsa_circ_95869,RMVar_hsa_circ_291413,RMVar_hsa_circ_354745,RMVar_hsa_circ_28740,RMVar_hsa_circ_64104,RMVar_hsa_circ_157807,RMVar_hsa_circ_293378,RMVar_hsa_circ_58858,RMVar_hsa_circ_157813,RMVar_hsa_circ_157814,RMVar_hsa_circ_32411,RMVar_hsa_circ_344029,RMVar_hsa_circ_51539,RMVar_hsa_circ_47350,RMVar_hsa_circ_157818,RMVar_hsa_circ_360174,RMVar_hsa_circ_330090,RMVar_hsa_circ_54301,RMVar_hsa_circ_157821,RMVar_hsa_circ_81252,RMVar_hsa_circ_357269,RMVar_hsa_circ_59746,RMVar_hsa_circ_36819,RMVar_hsa_circ_157823,RMVar_hsa_circ_361599,RMVar_hsa_circ_157825 32210 RMVar_ID_32210 Human_SNP_ID_503959359 A-to-I Human chr12 + 62556826 62556826 62556826 GGCTGGGCATGGTGGCTCATGCCTATAATCTCAACACTTCGGAAGGCTGAGGCAACAGGATAGCT GGCTGGGCATGGTGGCTCATGCCTATAATCTCCACACTTCGGAAGGCTGAGGCAACAGGATAGCT A C MON2 Ensembl:ENSG00000061987 Protein coding intron GSE47997;GSE107867 K562 cells&HepG2 cells;ASD brains,cerebellum - 23474544,30559470 RNA-Seq:(High) rs1565681987 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_809529,Human_RBP_ID_17205471,Human_RBP_ID_18630962 RMVar_hsa_circ_18305,RMVar_hsa_circ_95869,RMVar_hsa_circ_157814,RMVar_hsa_circ_51539,RMVar_hsa_circ_157818,RMVar_hsa_circ_81252,RMVar_hsa_circ_157823,RMVar_hsa_circ_45007,RMVar_hsa_circ_48200,RMVar_hsa_circ_56832,RMVar_hsa_circ_57783,RMVar_hsa_circ_58103,RMVar_hsa_circ_285588,RMVar_hsa_circ_157835,RMVar_hsa_circ_338553,RMVar_hsa_circ_157838,RMVar_hsa_circ_16390,RMVar_hsa_circ_75028,RMVar_hsa_circ_331877,RMVar_hsa_circ_266032,RMVar_hsa_circ_51588 32211 RMVar_ID_32211 Human_SNP_ID_503959387 A-to-I Human chr12 + 62556964 62556964 62556964 AAAATCATCCAAATGTGGTGGTGCACACCTGCAATCCCAGCTACTTGGGAGGCTGAGTTGCAAGG AAAATCATCCAAATGTGGTGGTGCACACCTGCTATCCCAGCTACTTGGGAGGCTGAGTTGCAAGG A T MON2 Ensembl:ENSG00000061987 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1425264348 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2346957,Human_RBP_ID_12000892 RMVar_hsa_circ_18305,RMVar_hsa_circ_95869,RMVar_hsa_circ_157814,RMVar_hsa_circ_51539,RMVar_hsa_circ_157818,RMVar_hsa_circ_81252,RMVar_hsa_circ_157823,RMVar_hsa_circ_45007,RMVar_hsa_circ_48200,RMVar_hsa_circ_56832,RMVar_hsa_circ_57783,RMVar_hsa_circ_58103,RMVar_hsa_circ_285588,RMVar_hsa_circ_157835,RMVar_hsa_circ_338553,RMVar_hsa_circ_157838,RMVar_hsa_circ_16390,RMVar_hsa_circ_75028,RMVar_hsa_circ_331877,RMVar_hsa_circ_266032,RMVar_hsa_circ_51588 32212 RMVar_ID_32212 Human_SNP_ID_503959397 A-to-I Human chr12 + 62556993 62556993 62556993 TGCAATCCCAGCTACTTGGGAGGCTGAGTTGCAAGGCTTGCTTGAGCCTGGGATGTGGAGGTTGC TGCAATCCCAGCTACTTGGGAGGCTGAGTTGCTAGGCTTGCTTGAGCCTGGGATGTGGAGGTTGC A T MON2 Ensembl:ENSG00000061987 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935137146 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12000893 RMVar_hsa_circ_18305,RMVar_hsa_circ_95869,RMVar_hsa_circ_157814,RMVar_hsa_circ_51539,RMVar_hsa_circ_157818,RMVar_hsa_circ_81252,RMVar_hsa_circ_157823,RMVar_hsa_circ_45007,RMVar_hsa_circ_48200,RMVar_hsa_circ_56832,RMVar_hsa_circ_57783,RMVar_hsa_circ_58103,RMVar_hsa_circ_285588,RMVar_hsa_circ_157835,RMVar_hsa_circ_338553,RMVar_hsa_circ_157838,RMVar_hsa_circ_16390,RMVar_hsa_circ_75028,RMVar_hsa_circ_331877,RMVar_hsa_circ_266032,RMVar_hsa_circ_51588 32213 RMVar_ID_32213 Human_SNP_ID_503959407 A-to-I Human chr12 + 62557037 62557037 62557037 AGCCTGGGATGTGGAGGTTGCTGCAGTTAGCCAAGATCGTGCCACTGCACTCAAGTCTGCGTGAC AGCCTGGGATGTGGAGGTTGCTGCAGTTAGCCGAGATCGTGCCACTGCACTCAAGTCTGCGTGAC A G MON2 Ensembl:ENSG00000061987 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,temporal_cortex - 29129909,30559470 RNA-Seq:(High) rs954162723 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12000894 RMVar_hsa_circ_18305,RMVar_hsa_circ_95869,RMVar_hsa_circ_157814,RMVar_hsa_circ_51539,RMVar_hsa_circ_157818,RMVar_hsa_circ_81252,RMVar_hsa_circ_157823,RMVar_hsa_circ_45007,RMVar_hsa_circ_48200,RMVar_hsa_circ_56832,RMVar_hsa_circ_57783,RMVar_hsa_circ_58103,RMVar_hsa_circ_285588,RMVar_hsa_circ_157835,RMVar_hsa_circ_338553,RMVar_hsa_circ_157838,RMVar_hsa_circ_16390,RMVar_hsa_circ_75028,RMVar_hsa_circ_331877,RMVar_hsa_circ_266032,RMVar_hsa_circ_51588 32214 RMVar_ID_32214 Human_SNP_ID_503959799 A-to-I Human chr12 + 62558178 62558178 62558178 TTTTGTATTTTTAGTAGAAACGGGATTTCTTCATGTTGGTCAGGCTAGTCTCAAACTCCTGACTT TTTTGTATTTTTAGTAGAAACGGGATTTCTTCCTGTTGGTCAGGCTAGTCTCAAACTCCTGACTT A C MON2 Ensembl:ENSG00000061987 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs970894274 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12000939 RMVar_hsa_circ_18305,RMVar_hsa_circ_95869,RMVar_hsa_circ_157814,RMVar_hsa_circ_51539,RMVar_hsa_circ_157818,RMVar_hsa_circ_81252,RMVar_hsa_circ_157823,RMVar_hsa_circ_45007,RMVar_hsa_circ_48200,RMVar_hsa_circ_56832,RMVar_hsa_circ_57783,RMVar_hsa_circ_58103,RMVar_hsa_circ_285588,RMVar_hsa_circ_157835,RMVar_hsa_circ_338553,RMVar_hsa_circ_157838,RMVar_hsa_circ_16390,RMVar_hsa_circ_75028,RMVar_hsa_circ_331877,RMVar_hsa_circ_266032,RMVar_hsa_circ_51588 32215 RMVar_ID_32215 Human_SNP_ID_503960060 A-to-I Human chr12 + 62559481 62559481 62559481 CATGGGCAACATGGTGAAACCCTATCTCTACAAAAAATACAAAAATTAGCCAAGTGTGGTGGTGT CATGGGCAACATGGTGAAACCCTATCTCTACAGAAAATACAAAAATTAGCCAAGTGTGGTGGTGT A G MON2 Ensembl:ENSG00000061987 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1017865665 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12000979 RMVar_hsa_circ_18305,RMVar_hsa_circ_95869,RMVar_hsa_circ_157814,RMVar_hsa_circ_51539,RMVar_hsa_circ_157818,RMVar_hsa_circ_81252,RMVar_hsa_circ_157823,RMVar_hsa_circ_45007,RMVar_hsa_circ_48200,RMVar_hsa_circ_56832,RMVar_hsa_circ_57783,RMVar_hsa_circ_58103,RMVar_hsa_circ_285588,RMVar_hsa_circ_157835,RMVar_hsa_circ_338553,RMVar_hsa_circ_157838,RMVar_hsa_circ_16390,RMVar_hsa_circ_75028,RMVar_hsa_circ_331877,RMVar_hsa_circ_266032,RMVar_hsa_circ_51588 32216 RMVar_ID_32216 Human_SNP_ID_503963191 A-to-I Human chr12 + 62573480 62573480 62573480 CAAGGTGTGGTGACACACCTGTAATCCCAGCTACTTTGGGAGGCTGAGGTGGGAGGATTGCCGAG CAAGGTGTGGTGACACACCTGTAATCCCAGCTGCTTTGGGAGGCTGAGGTGGGAGGATTGCCGAG A G MON2 Ensembl:ENSG00000061987 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1389150491 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24990105 RMVar_hsa_circ_421,RMVar_hsa_circ_18305,RMVar_hsa_circ_51539,RMVar_hsa_circ_157818,RMVar_hsa_circ_81252,RMVar_hsa_circ_157823,RMVar_hsa_circ_48200,RMVar_hsa_circ_75028,RMVar_hsa_circ_331877,RMVar_hsa_circ_266032,RMVar_hsa_circ_32142,RMVar_hsa_circ_327174,RMVar_hsa_circ_348131,RMVar_hsa_circ_157841,RMVar_hsa_circ_304697,RMVar_hsa_circ_347672,RMVar_hsa_circ_323949,RMVar_hsa_circ_288231,RMVar_hsa_circ_157842,RMVar_hsa_circ_157843 32217 RMVar_ID_32217 Human_SNP_ID_503963406 A-to-I Human chr12 + 62574451 62574451 62574451 CAGGCTGGAGTGAAGTCGCATGTTCATGGCTCACTGCGGCCTTGACCTCCTGGCCTCAGGTGATT CAGGCTGGAGTGAAGTCGCATGTTCATGGCTCCCTGCGGCCTTGACCTCCTGGCCTCAGGTGATT A C MON2 Ensembl:ENSG00000061987 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1226257951 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_421,RMVar_hsa_circ_18305,RMVar_hsa_circ_51539,RMVar_hsa_circ_157818,RMVar_hsa_circ_81252,RMVar_hsa_circ_157823,RMVar_hsa_circ_48200,RMVar_hsa_circ_75028,RMVar_hsa_circ_331877,RMVar_hsa_circ_266032,RMVar_hsa_circ_32142,RMVar_hsa_circ_327174,RMVar_hsa_circ_348131,RMVar_hsa_circ_157841,RMVar_hsa_circ_304697,RMVar_hsa_circ_347672,RMVar_hsa_circ_323949,RMVar_hsa_circ_288231,RMVar_hsa_circ_157842,RMVar_hsa_circ_157843 32218 RMVar_ID_32218 Human_SNP_ID_503963420 A-to-I Human chr12 + 62574506 62574506 62574506 TCAGGTGATTCTCCCACCTCAGCCTCTCTTGTAGCTCGGACTATAGGCATGCACCACCACACCCA TCAGGTGATTCTCCCACCTCAGCCTCTCTTGTCGCTCGGACTATAGGCATGCACCACCACACCCA A C MON2 Ensembl:ENSG00000061987 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs914662720 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_421,RMVar_hsa_circ_18305,RMVar_hsa_circ_51539,RMVar_hsa_circ_157818,RMVar_hsa_circ_81252,RMVar_hsa_circ_157823,RMVar_hsa_circ_48200,RMVar_hsa_circ_75028,RMVar_hsa_circ_331877,RMVar_hsa_circ_266032,RMVar_hsa_circ_32142,RMVar_hsa_circ_327174,RMVar_hsa_circ_348131,RMVar_hsa_circ_157841,RMVar_hsa_circ_304697,RMVar_hsa_circ_347672,RMVar_hsa_circ_323949,RMVar_hsa_circ_288231,RMVar_hsa_circ_157842,RMVar_hsa_circ_157843 32219 RMVar_ID_32219 Human_SNP_ID_503963511 A-to-I Human chr12 + 62574983 62574983 62574983 CCGCCTCTACAAAAAAAATTTAAAAATTAGCCAGATATGGTGGCATGTGCCTGTAGTCCCAGCTA CCGCCTCTACAAAAAAAATTTAAAAATTAGCCGGATATGGTGGCATGTGCCTGTAGTCCCAGCTA A G MON2 Ensembl:ENSG00000061987 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054661955 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_421,RMVar_hsa_circ_18305,RMVar_hsa_circ_51539,RMVar_hsa_circ_157818,RMVar_hsa_circ_81252,RMVar_hsa_circ_157823,RMVar_hsa_circ_48200,RMVar_hsa_circ_75028,RMVar_hsa_circ_331877,RMVar_hsa_circ_266032,RMVar_hsa_circ_32142,RMVar_hsa_circ_327174,RMVar_hsa_circ_348131,RMVar_hsa_circ_157841,RMVar_hsa_circ_304697,RMVar_hsa_circ_347672,RMVar_hsa_circ_323949,RMVar_hsa_circ_288231,RMVar_hsa_circ_157842,RMVar_hsa_circ_157843 32220 RMVar_ID_32220 Human_SNP_ID_504006858 A-to-I Human chr12 - 62755869 62755869 62755869 TTTAGCTCAGGGATGACCTTGCCCACAACCTTAGCAGCACCAGTAGAGGCAGGGATGATGTTCTG TTTAGCTCAGGGATGACCTTGCCCACAACCTTGGCAGCACCAGTAGAGGCAGGGATGATGTTCTG T C PPM1H Ensembl:ENSG00000111110 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1422265872 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64649 32221 RMVar_ID_32221 Human_SNP_ID_504056371 A-to-I Human chr12 + 62965309 62965309 62965309 ATTAGCATAAAAAAGATAATAGTGGCCTTCTCACCTAACGCCACCAACATGGTGTTCAGGCGCTT ATTAGCATAAAAAAGATAATAGTGGCCTTCTCCCCTAACGCCACCAACATGGTGTTCAGGCGCTT A C - - Other Unknown GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs536790318 Functional Loss SNV dbSNP153 33..33 33 - - - 32222 RMVar_ID_32222 Human_SNP_ID_504056378 A-to-I Human chr12 + 62965319 62965319 62965319 AAAAGATAATAGTGGCCTTCTCACCTAACGCCACCAACATGGTGTTCAGGCGCTTCGTGGAGGTT AAAAGATAATAGTGGCCTTCTCACCTAACGCCGCCAACATGGTGTTCAGGCGCTTCGTGGAGGTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878991008 Functional Loss SNV dbSNP153 33..33 33 - - - 32223 RMVar_ID_32223 Human_SNP_ID_504056439 A-to-I Human chr12 + 62965545 62965545 62965545 GTTTCCGCACAGTGCCCGCCAAAAGTATGTCCAACAAGCCTGGCAGAAGGCAGACATCAATACAA GTTTCCGCACAGTGCCCGCCAAAAGTATGTCCGACAAGCCTGGCAGAAGGCAGACATCAATACAA A G RPL14P1 Ensembl:ENSG00000139239 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879234821 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123760,RMVar_hsa_circ_157846 32224 RMVar_ID_32224 Human_SNP_ID_504253797 A-to-I Human chr12 + 63795106 63795106 63795106 TCGTTTTGAGCTCAGGAGTTTGAGACCAGCCTAGGCAGCATGGCGAAACTGTATCTCTACAAAAA TCGTTTTGAGCTCAGGAGTTTGAGACCAGCCTGGGCAGCATGGCGAAACTGTATCTCTACAAAAA A G RXYLT1 Ensembl:ENSG00000118600 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1228927551 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_354698 32225 RMVar_ID_32225 Human_SNP_ID_504260169 A-to-I Human chr12 + 63822640 63822640 63822640 TCGGAGAAGACATGGATGATGAGCGCCTTAAGAATCTCTTTGGCAAGTTTGGGCCTGCCTTAAAT TCGGAGAAGACATGGATGATGAGCGCCTTAAGGATCTCTTTGGCAAGTTTGGGCCTGCCTTAAAT A G PABPC1P4 Ensembl:ENSG00000255642 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1347493559 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_425395,Human_RBP_ID_2347680,Human_RBP_ID_4258378,Human_RBP_ID_6239657,Human_RBP_ID_26423901,Human_RBP_ID_26910112 32226 RMVar_ID_32226 Human_SNP_ID_504265886 A-to-I Human chr12 + 63847476 63847476 63847476 GTGTGGGACTCATTAAGACATAAGTCTAGGCCAGGCACGGTGGCTCACGCCTGTAATCCCAGCAC GTGTGGGACTCATTAAGACATAAGTCTAGGCCGGGCACGGTGGCTCACGCCTGTAATCCCAGCAC A G SRGAP1 Ensembl:ENSG00000196935 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1440274580 Functional Loss SNV dbSNP153 33..33 33 - - - 32227 RMVar_ID_32227 Human_SNP_ID_504344805 A-to-I Human chr12 - 64191812 64191812 64191812 CCTCGGCCTCCCAAAGCACTGGGTTTATAAGCATGTGCCACTGCACCTGGCCTCCTTTCTTTTTC CCTCGGCCTCCCAAAGCACTGGGTTTATAAGCGTGTGCCACTGCACCTGGCCTCCTTTCTTTTTC T C C12orf66 Ensembl:ENSG00000174206 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1371362491 Functional Loss SNV dbSNP153 33..33 33 - - - 32228 RMVar_ID_32228 Human_SNP_ID_504344810 A-to-I Human chr12 - 64191827 64191827 64191827 CACATGAGCCTCCCGCCTCGGCCTCCCAAAGCACTGGGTTTATAAGCATGTGCCACTGCACCTGG CACATGAGCCTCCCGCCTCGGCCTCCCAAAGCGCTGGGTTTATAAGCATGTGCCACTGCACCTGG T C C12orf66 Ensembl:ENSG00000174206 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1439044795 Functional Loss SNV dbSNP153 33..33 33 - - - 32229 RMVar_ID_32229 Human_SNP_ID_504344818 A-to-I Human chr12 - 64191856 64191856 64191856 TGCTCGGGCTGGACTCAAACTCCTGGACTCACATGAGCCTCCCGCCTCGGCCTCCCAAAGCACTG TGCTCGGGCTGGACTCAAACTCCTGGACTCACGTGAGCCTCCCGCCTCGGCCTCCCAAAGCACTG T C C12orf66 Ensembl:ENSG00000174206 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1380730406 Functional Loss SNV dbSNP153 33..33 33 - - - 32230 RMVar_ID_32230 Human_SNP_ID_504344832 A-to-I Human chr12 - 64191892 64191890 64191892 ACAGGCATGAGCCATCACACCTGGGTCTCACTATGTTGCTCGGGCTGGACTCAAACTCCTGGACT ACAGGCATGAGCCATCACACCTGGGTCTCACT__GTTGCTCGGGCTGGACTCAAACTCCTGGACT CAT C C12orf66 Ensembl:ENSG00000174206 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1483172388 Functional Loss DEL dbSNP153 33..34 33 - - - 32231 RMVar_ID_32231 Human_SNP_ID_504344834 A-to-I Human chr12 - 64191892 64191892 64191892 ACAGGCATGAGCCATCACACCTGGGTCTCACTATGTTGCTCGGGCTGGACTCAAACTCCTGGACT ACAGGCATGAGCCATCACACCTGGGTCTCACTGTGTTGCTCGGGCTGGACTCAAACTCCTGGACT T C C12orf66 Ensembl:ENSG00000174206 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1288654559 Functional Loss SNV dbSNP153 33..33 33 - - - 32232 RMVar_ID_32232 Human_SNP_ID_504344853 A-to-I Human chr12 - 64191951 64191951 64191951 GCCTCAACCTCCTGGGCTCAAGTGATCCTCCCACATCAGCATCCCGAGTAGGTGGGATTACAGGC GCCTCAACCTCCTGGGCTCAAGTGATCCTCCCGCATCAGCATCCCGAGTAGGTGGGATTACAGGC T C C12orf66 Ensembl:ENSG00000174206 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1259115403 Functional Loss SNV dbSNP153 33..33 33 - - - 32233 RMVar_ID_32233 Human_SNP_ID_504344865 A-to-I Human chr12 - 64192000 64192000 64192000 TGTCTGTTTTCCAGGCTGGAGTACAGTGGCACAATCACAACTCACTGCAGCCTCAACCTCCTGGG TGTCTGTTTTCCAGGCTGGAGTACAGTGGCACGATCACAACTCACTGCAGCCTCAACCTCCTGGG T C C12orf66 Ensembl:ENSG00000174206 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs904334089 Functional Loss SNV dbSNP153 33..33 33 - - - 32234 RMVar_ID_32234 Human_SNP_ID_504378809 A-to-I Human chr12 - 64338751 64338751 64338751 GCAATGCTGACATGCAAAAGCAGATAAAGCATATGATGGCTTTCATTGAACAAGAAGCCAATGAG GCAATGCTGACATGCAAAAGCAGATAAAGCATGTGATGGCTTTCATTGAACAAGAAGCCAATGAG T C AC135279.3,C12orf56 Ensembl:ENSG00000256293,Ensembl:ENSG00000185306 Pseudogene,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1448279242 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_425429 RMVar_hsa_circ_53606 32235 RMVar_ID_32235 Human_SNP_ID_504378815 A-to-I Human chr12 - 64338772 64338772 64338772 TTGCTCTCACCATGGCTCTCAGCAATGCTGACATGCAAAAGCAGATAAAGCATATGATGGCTTTC TTGCTCTCACCATGGCTCTCAGCAATGCTGACGTGCAAAAGCAGATAAAGCATATGATGGCTTTC T C AC135279.3,C12orf56 Ensembl:ENSG00000256293,Ensembl:ENSG00000185306 Pseudogene,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878989790 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1853119 RMVar_hsa_circ_53606 32236 RMVar_ID_32236 Human_SNP_ID_504378819 A-to-I Human chr12 - 64338781 64338781 64338781 GGCCTAGCTTTGCTCTCACCATGGCTCTCAGCAATGCTGACATGCAAAAGCAGATAAAGCATATG GGCCTAGCTTTGCTCTCACCATGGCTCTCAGCGATGCTGACATGCAAAAGCAGATAAAGCATATG T C AC135279.3,C12orf56 Ensembl:ENSG00000256293,Ensembl:ENSG00000185306 Pseudogene,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878863191 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1853119 RMVar_hsa_circ_53606 32237 RMVar_ID_32237 Human_SNP_ID_504378825 A-to-I Human chr12 - 64338796 64338796 64338796 AGCCTGCTGCTCACCGGCCTAGCTTTGCTCTCACCATGGCTCTCAGCAATGCTGACATGCAAAAG AGCCTGCTGCTCACCGGCCTAGCTTTGCTCTCGCCATGGCTCTCAGCAATGCTGACATGCAAAAG T C AC135279.3,C12orf56 Ensembl:ENSG00000256293,Ensembl:ENSG00000185306 Pseudogene,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879244248 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_53606 32238 RMVar_ID_32238 Human_SNP_ID_504395138 A-to-I Human chr12 + 64405868 64405868 64405868 TCGATCTCTTGACCTCGCGATCCGCCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG TCGATCTCTTGACCTCGCGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG A G XPOT Ensembl:ENSG00000184575 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1230518620 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12003360 RMVar_hsa_circ_82472,RMVar_hsa_circ_157898 32239 RMVar_ID_32239 Human_SNP_ID_504395145 A-to-I Human chr12 + 64405890 64405890 64405890 CGCCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCCCGGCCTTCCACT CGCCCGCCTCAGCCTCCCAAAGTGCTGGGATTGCAGGCGTGAGCCACCGCGCCCGGCCTTCCACT A G XPOT Ensembl:ENSG00000184575 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1465476732 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82472,RMVar_hsa_circ_157898 32240 RMVar_ID_32240 Human_SNP_ID_504395561 A-to-I Human chr12 + 64407223 64407223 64407223 TTAAGATTGTGAGAAATGGCCGGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGTC TTAAGATTGTGAGAAATGGCCGGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGTC A G XPOT Ensembl:ENSG00000184575 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs976459414 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82472,RMVar_hsa_circ_157898 32241 RMVar_ID_32241 Human_SNP_ID_504395602 A-to-I Human chr12 + 64407365 64407365 64407365 AAAATTAGCCGGGTGTGGTGGCTCACCCCTGTAATCTCAGCTATTTGGGAGGCTGAGGCAGAAGA AAAATTAGCCGGGTGTGGTGGCTCACCCCTGTCATCTCAGCTATTTGGGAGGCTGAGGCAGAAGA A C XPOT Ensembl:ENSG00000184575 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1037405396 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82472,RMVar_hsa_circ_157898 32242 RMVar_ID_32242 Human_SNP_ID_504395780 A-to-I Human chr12 + 64408133 64408132 64408134 GCCCCACAGCCTTTTTTTGTTTTTTTTGAGACAGAGTCTCGTTCTGTCACCCAGGCTGGAGTGCA GCCCCACAGCCTTTTTTTGTTTTTTTTGAGAC__AGTCTCGTTCTGTCACCCAGGCTGGAGTGCA CAG C XPOT Ensembl:ENSG00000184575 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1438631592 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_114674 RMVar_hsa_circ_82472,RMVar_hsa_circ_157898 32243 RMVar_ID_32243 Human_SNP_ID_504395781 A-to-I Human chr12 + 64408133 64408133 64408133 GCCCCACAGCCTTTTTTTGTTTTTTTTGAGACAGAGTCTCGTTCTGTCACCCAGGCTGGAGTGCA GCCCCACAGCCTTTTTTTGTTTTTTTTGAGACCGAGTCTCGTTCTGTCACCCAGGCTGGAGTGCA A C XPOT Ensembl:ENSG00000184575 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs754552209 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_114674 RMVar_hsa_circ_82472,RMVar_hsa_circ_157898 32244 RMVar_ID_32244 Human_SNP_ID_504395782 A-to-I Human chr12 + 64408133 64408133 64408133 GCCCCACAGCCTTTTTTTGTTTTTTTTGAGACAGAGTCTCGTTCTGTCACCCAGGCTGGAGTGCA GCCCCACAGCCTTTTTTTGTTTTTTTTGAGACGGAGTCTCGTTCTGTCACCCAGGCTGGAGTGCA A G XPOT Ensembl:ENSG00000184575 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs754552209 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_114674 RMVar_hsa_circ_82472,RMVar_hsa_circ_157898 32245 RMVar_ID_32245 Human_SNP_ID_504395930 A-to-I Human chr12 + 64408699 64408699 64408699 TTTTTTTGTGTGTTTTGTTTTTTTTGAGATGGAATCTCACTCTGTTCTCCAGGCTGGAGTGCAGT TTTTTTTGTGTGTTTTGTTTTTTTTGAGATGGCATCTCACTCTGTTCTCCAGGCTGGAGTGCAGT A C XPOT Ensembl:ENSG00000184575 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1262788447 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3410824,Human_RBP_ID_12003515,Human_RBP_ID_24990842 RMVar_hsa_circ_82472,RMVar_hsa_circ_157898 32246 RMVar_ID_32246 Human_SNP_ID_504395945 A-to-I Human chr12 + 64408751 64408751 64408751 GCTGGAGTGCAGTGGCGCAATCTTGGCTCACTACAACCTCTGCCTCCTGGGTTCAAGCGATTCTT GCTGGAGTGCAGTGGCGCAATCTTGGCTCACTGCAACCTCTGCCTCCTGGGTTCAAGCGATTCTT A G XPOT Ensembl:ENSG00000184575 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1399799995 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82472,RMVar_hsa_circ_157898 32247 RMVar_ID_32247 Human_SNP_ID_504396208 A-to-I Human chr12 + 64409614 64409614 64409614 AAAATTAGCCCAGCGCGGTGGCGGGCGCCTGTAGTCCCAGCTACTCGGGAGGGTGAGGCAGGAGA AAAATTAGCCCAGCGCGGTGGCGGGCGCCTGTGGTCCCAGCTACTCGGGAGGGTGAGGCAGGAGA A G XPOT Ensembl:ENSG00000184575 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1229081746 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23306061 RMVar_hsa_circ_82472,RMVar_hsa_circ_157898 32248 RMVar_ID_32248 Human_SNP_ID_504396249 A-to-I Human chr12 + 64409714 64409714 64409714 CTGATACGGTGCCACTGCACTCCAGCCTGGGCAACAGAGTGAGACTCCGTCTCAAAAAAAAAAAT CTGATACGGTGCCACTGCACTCCAGCCTGGGCGACAGAGTGAGACTCCGTCTCAAAAAAAAAAAT A G XPOT Ensembl:ENSG00000184575 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs936731534 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82472,RMVar_hsa_circ_157898 32249 RMVar_ID_32249 Human_SNP_ID_504396250 A-to-I Human chr12 + 64409714 64409714 64409714 CTGATACGGTGCCACTGCACTCCAGCCTGGGCAACAGAGTGAGACTCCGTCTCAAAAAAAAAAAT CTGATACGGTGCCACTGCACTCCAGCCTGGGCTACAGAGTGAGACTCCGTCTCAAAAAAAAAAAT A T XPOT Ensembl:ENSG00000184575 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs936731534 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82472,RMVar_hsa_circ_157898 32250 RMVar_ID_32250 Human_SNP_ID_504396251 A-to-I Human chr12 + 64409717 64409717 64409717 ATACGGTGCCACTGCACTCCAGCCTGGGCAACAGAGTGAGACTCCGTCTCAAAAAAAAAAATCAG ATACGGTGCCACTGCACTCCAGCCTGGGCAACTGAGTGAGACTCCGTCTCAAAAAAAAAAATCAG A T XPOT Ensembl:ENSG00000184575 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1053652648 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82472,RMVar_hsa_circ_157898 32251 RMVar_ID_32251 Human_SNP_ID_504399280 A-to-I Human chr12 + 64422044 64422044 64422044 GTTGGTCAGGCTGGTCTTGAACTCCCTACCTCAGGTGATCTGCCCACCACAGCCTCCCAAAGTGC GTTGGTCAGGCTGGTCTTGAACTCCCTACCTCGGGTGATCTGCCCACCACAGCCTCCCAAAGTGC A G XPOT Ensembl:ENSG00000184575 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1038710909 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38465,RMVar_hsa_circ_355743,RMVar_hsa_circ_356517,RMVar_hsa_circ_366999,RMVar_hsa_circ_376369,RMVar_hsa_circ_360432,RMVar_hsa_circ_356115,RMVar_hsa_circ_339982,RMVar_hsa_circ_310416,RMVar_hsa_circ_74887,RMVar_hsa_circ_295877,RMVar_hsa_circ_62519,RMVar_hsa_circ_63505,RMVar_hsa_circ_39289,RMVar_hsa_circ_33371,RMVar_hsa_circ_157899,RMVar_hsa_circ_157900,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_64441,RMVar_hsa_circ_157912,RMVar_hsa_circ_116565,RMVar_hsa_circ_41214,RMVar_hsa_circ_340024 32252 RMVar_ID_32252 Human_SNP_ID_504400306 A-to-I Human chr12 + 64426060 64426060 64426060 AAAATGTAGGCCAGGTATGGTGGCTCATGCCTATAATCCCAACACTCTGGGAGGCCGATCACAAG AAAATGTAGGCCAGGTATGGTGGCTCATGCCTGTAATCCCAACACTCTGGGAGGCCGATCACAAG A G XPOT Ensembl:ENSG00000184575 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1049026328 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24990983 RMVar_hsa_circ_17784,RMVar_hsa_circ_355743,RMVar_hsa_circ_356517,RMVar_hsa_circ_356115,RMVar_hsa_circ_339982,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_328343,RMVar_hsa_circ_19183,RMVar_hsa_circ_56520,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_157917,RMVar_hsa_circ_125827,RMVar_hsa_circ_157921,RMVar_hsa_circ_81030,RMVar_hsa_circ_157920,RMVar_hsa_circ_369963,RMVar_hsa_circ_157922 32253 RMVar_ID_32253 Human_SNP_ID_504400500 A-to-I Human chr12 + 64426767 64426767 64426767 CACTTTGGGAGGCTGAGGCGGGTGGATCACCTAAGATCAGGAGTTTGAGACTAGCCTGGCCAACA CACTTTGGGAGGCTGAGGCGGGTGGATCACCTCAGATCAGGAGTTTGAGACTAGCCTGGCCAACA A C XPOT Ensembl:ENSG00000184575 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs961417294 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17784,RMVar_hsa_circ_355743,RMVar_hsa_circ_356517,RMVar_hsa_circ_356115,RMVar_hsa_circ_339982,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_328343,RMVar_hsa_circ_19183,RMVar_hsa_circ_56520,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_157917,RMVar_hsa_circ_125827,RMVar_hsa_circ_157921,RMVar_hsa_circ_81030,RMVar_hsa_circ_157920,RMVar_hsa_circ_369963,RMVar_hsa_circ_157922 32254 RMVar_ID_32254 Human_SNP_ID_504400646 A-to-I Human chr12 + 64427285 64427285 64427285 AGGATTACAGGTGTCCATCGCCACACCCGGCTAATTTTTTGTATTTTTAGTAGAGATGGGGCTTC AGGATTACAGGTGTCCATCGCCACACCCGGCTCATTTTTTGTATTTTTAGTAGAGATGGGGCTTC A C XPOT Ensembl:ENSG00000184575 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs112594016 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17784,RMVar_hsa_circ_355743,RMVar_hsa_circ_356517,RMVar_hsa_circ_356115,RMVar_hsa_circ_339982,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_328343,RMVar_hsa_circ_19183,RMVar_hsa_circ_56520,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_157917,RMVar_hsa_circ_125827,RMVar_hsa_circ_157921,RMVar_hsa_circ_81030,RMVar_hsa_circ_157920,RMVar_hsa_circ_369963,RMVar_hsa_circ_157922 32255 RMVar_ID_32255 Human_SNP_ID_504400647 A-to-I Human chr12 + 64427285 64427285 64427285 AGGATTACAGGTGTCCATCGCCACACCCGGCTAATTTTTTGTATTTTTAGTAGAGATGGGGCTTC AGGATTACAGGTGTCCATCGCCACACCCGGCTGATTTTTTGTATTTTTAGTAGAGATGGGGCTTC A G XPOT Ensembl:ENSG00000184575 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs112594016 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17784,RMVar_hsa_circ_355743,RMVar_hsa_circ_356517,RMVar_hsa_circ_356115,RMVar_hsa_circ_339982,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_328343,RMVar_hsa_circ_19183,RMVar_hsa_circ_56520,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_157917,RMVar_hsa_circ_125827,RMVar_hsa_circ_157921,RMVar_hsa_circ_81030,RMVar_hsa_circ_157920,RMVar_hsa_circ_369963,RMVar_hsa_circ_157922 32256 RMVar_ID_32256 Human_SNP_ID_504403675 A-to-I Human chr12 + 64440190 64440190 64440190 CCATTCTACTCTCTGATTCTGTGAATTTGACTACTTTAGATACCTAATATAAGTGGAATCATGCA CCATTCTACTCTCTGATTCTGTGAATTTGACTGCTTTAGATACCTAATATAAGTGGAATCATGCA A G XPOT Ensembl:ENSG00000184575 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984443790 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12004282 RMVar_hsa_circ_356517 32257 RMVar_ID_32257 Human_SNP_ID_504405663 A-to-I Human chr12 + 64449066 64449066 64449066 ACTAAAAATACAACAGCCAGGTGTGATGGTGCACGCTCGTAATCCCGGCTACTCAGGAGGCTGAG ACTAAAAATACAACAGCCAGGTGTGATGGTGCGCGCTCGTAATCCCGGCTACTCAGGAGGCTGAG A G XPOT Ensembl:ENSG00000184575 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1455885753 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_425523,Human_RBP_ID_6207468,Human_RBP_ID_26418867 32258 RMVar_ID_32258 Human_SNP_ID_504405674 A-to-I Human chr12 + 64449084 64449084 64449084 AGGTGTGATGGTGCACGCTCGTAATCCCGGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAA AGGTGTGATGGTGCACGCTCGTAATCCCGGCTCCTCAGGAGGCTGAGGCAGGAGAATCGCTTGAA A C XPOT Ensembl:ENSG00000184575 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1137583 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26418867 32259 RMVar_ID_32259 Human_SNP_ID_504405975 A-to-I Human chr12 + 64450358 64450358 64450358 TTTGGTAGAGACAGGGTCTCACTATGTTACCCAGTCTGGTCTCAAACTCCCGGCCTCAAGCAATC TTTGGTAGAGACAGGGTCTCACTATGTTACCCTGTCTGGTCTCAAACTCCCGGCCTCAAGCAATC A T XPOT Ensembl:ENSG00000184575 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1182415122 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6207507,Human_RBP_ID_12004588,Human_RBP_ID_26418885 32260 RMVar_ID_32260 Human_SNP_ID_504409338 A-to-I Human chr12 + 64463544 64463544 64463544 AACATAGTGAGACCCCGTCTCTACAAAATAATAGAAAAATTAGCCAGGCATGGTGGAGCATGCCC AACATAGTGAGACCCCGTCTCTACAAAATAATGGAAAAATTAGCCAGGCATGGTGGAGCATGCCC A G TBK1 Ensembl:ENSG00000183735 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs958145833 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10484,RMVar_hsa_circ_307023,RMVar_hsa_circ_157925,RMVar_hsa_circ_114688,RMVar_hsa_circ_328086,RMVar_hsa_circ_361887,RMVar_hsa_circ_72810,RMVar_hsa_circ_297203,RMVar_hsa_circ_16705,RMVar_hsa_circ_17422,RMVar_hsa_circ_157926,RMVar_hsa_circ_157927,RMVar_hsa_circ_157928,RMVar_hsa_circ_285743,RMVar_hsa_circ_320650,RMVar_hsa_circ_362957,RMVar_hsa_circ_64740 32261 RMVar_ID_32261 Human_SNP_ID_504415758 A-to-I Human chr12 + 64491359 64491359 64491359 TACTGTACTCTTGGCTGGGTGTGGTGGCTCACACCTCTAATCCCAGCACTTTGGGAGGCTGAGTC TACTGTACTCTTGGCTGGGTGTGGTGGCTCACGCCTCTAATCCCAGCACTTTGGGAGGCTGAGTC A G TBK1 Ensembl:ENSG00000183735 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs544320715 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12005054 RMVar_hsa_circ_16705,RMVar_hsa_circ_285743,RMVar_hsa_circ_348046,RMVar_hsa_circ_61885 32262 RMVar_ID_32262 Human_SNP_ID_504416283 A-to-I Human chr12 + 64493506 64493506 64493506 AAAATTAGCCGGGCGTAGTGGCAGACGCTTGTAATCCCAGCTACTGGGGAGGCTGAGGCAAGAGA AAAATTAGCCGGGCGTAGTGGCAGACGCTTGTCATCCCAGCTACTGGGGAGGCTGAGGCAAGAGA A C TBK1 Ensembl:ENSG00000183735 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1430662990 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16705,RMVar_hsa_circ_285743,RMVar_hsa_circ_348046,RMVar_hsa_circ_61885 32263 RMVar_ID_32263 Human_SNP_ID_504416414 A-to-I Human chr12 + 64494200 64494200 64494200 TATAAAAATTTAAGCTGGGCACAGTGGCTCATACCTGTAATCCCAGCACTTTGGGAGGCCAAGGT TATAAAAATTTAAGCTGGGCACAGTGGCTCATTCCTGTAATCCCAGCACTTTGGGAGGCCAAGGT A T TBK1 Ensembl:ENSG00000183735 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs953730607 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16705,RMVar_hsa_circ_285743,RMVar_hsa_circ_348046,RMVar_hsa_circ_61885 32264 RMVar_ID_32264 Human_SNP_ID_504416481 A-to-I Human chr12 + 64494372 64494372 64494372 GCAATAGCACGCACTTGTAATCCCATCTACTCAGGAGGCTTAAGGTGAGAGGATGGCTTGAACTC GCAATAGCACGCACTTGTAATCCCATCTACTCGGGAGGCTTAAGGTGAGAGGATGGCTTGAACTC A G TBK1 Ensembl:ENSG00000183735 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1036828918 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16705,RMVar_hsa_circ_285743,RMVar_hsa_circ_348046,RMVar_hsa_circ_61885 32265 RMVar_ID_32265 Human_SNP_ID_504417493 A-to-I Human chr12 + 64498694 64498694 64498694 TATTTCACATTTGGCCAGGCACGGTGGCTCACACCTGTAATCCTAGCACTTTGGGAAGCCAAGGC TATTTCACATTTGGCCAGGCACGGTGGCTCACGCCTGTAATCCTAGCACTTTGGGAAGCCAAGGC A G TBK1 Ensembl:ENSG00000183735 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs959494815 Functional Loss SNV dbSNP153 33..33 33 - - - 32266 RMVar_ID_32266 Human_SNP_ID_504417521 A-to-I Human chr12 + 64498852 64498852 64498852 GTGGTGCACACCTGTAATCCCAGCTACTGGGGAGGCTGAGGCACGAGAATCACCTGAATCTGGGA GTGGTGCACACCTGTAATCCCAGCTACTGGGGGGGCTGAGGCACGAGAATCACCTGAATCTGGGA A G TBK1 Ensembl:ENSG00000183735 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1028560008 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_116915 32267 RMVar_ID_32267 Human_SNP_ID_504449319 A-to-I Human chr12 + 64628595 64628595 64628595 CTTGGCTCACTGCAACCCCACCTCCCAGGTTCAAGCAATTCTGCCTGCCTCAGCCTCCCGAGTAG CTTGGCTCACTGCAACCCCACCTCCCAGGTTCCAGCAATTCTGCCTGCCTCAGCCTCCCGAGTAG A C RASSF3,AC078962.2 Ensembl:ENSG00000153179,Ensembl:ENSG00000225195 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1209531481 Functional Loss SNV dbSNP153 33..33 33 - - - 32268 RMVar_ID_32268 Human_SNP_ID_504449783 A-to-I Human chr12 + 64630451 64630451 64630451 GGGAGGCTGAGGCAAGAGGTTTGCTTGAGCTTAGCAGTTTGAGGCTGCAGTGAGCTATGGTCACA GGGAGGCTGAGGCAAGAGGTTTGCTTGAGCTTTGCAGTTTGAGGCTGCAGTGAGCTATGGTCACA A T RASSF3 Ensembl:ENSG00000153179 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1045569974 Functional Loss SNV dbSNP153 33..33 33 - - - 32269 RMVar_ID_32269 Human_SNP_ID_504450560 A-to-I Human chr12 + 64633845 64633845 64633845 AGAGACTGATTAAATTTGACCAAAATGCTGATAGAAATATGGACCAAGTGGGGTGGCTCACGCCT AGAGACTGATTAAATTTGACCAAAATGCTGATGGAAATATGGACCAAGTGGGGTGGCTCACGCCT A G RASSF3 Ensembl:ENSG00000153179 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1434872353 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22574834 32270 RMVar_ID_32270 Human_SNP_ID_504463519 A-to-I Human chr12 + 64685269 64685269 64685269 GTAAGGTTTTTTGTTTTGTTTTGTTTTGAAACAAGGTTTTGCTCTGTCACCTGGGCTGGAGAGCA GTAAGGTTTTTTGTTTTGTTTTGTTTTGAAACTAGGTTTTGCTCTGTCACCTGGGCTGGAGAGCA A T RASSF3 Ensembl:ENSG00000153179 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1326786255 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33112,RMVar_hsa_circ_310147,RMVar_hsa_circ_377685,RMVar_hsa_circ_157935 32271 RMVar_ID_32271 Human_SNP_ID_504463818 A-to-I Human chr12 + 64686531 64686531 64686531 TACGCGGGAGGCTGAGGCAGAAGAATGGCGTGAACCCAGGAGGCAGAGCTTGCAGTGAGGCAAGA TACGCGGGAGGCTGAGGCAGAAGAATGGCGTGGACCCAGGAGGCAGAGCTTGCAGTGAGGCAAGA A G RASSF3 Ensembl:ENSG00000153179 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs990400873 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33112,RMVar_hsa_circ_310147,RMVar_hsa_circ_377685,RMVar_hsa_circ_157935 32272 RMVar_ID_32272 Human_SNP_ID_504471468 A-to-I Human chr12 - 64715479 64715479 64715479 GAGTCTCACTATGTCACCCAGGCTGGAGTGCAATGGCATGATCTCAGCTCACTGCAACCTTCGCC GAGTCTCACTATGTCACCCAGGCTGGAGTGCAGTGGCATGATCTCAGCTCACTGCAACCTTCGCC T C GNS Ensembl:ENSG00000135677 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1177284696 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_684302,Human_miRNA_ID_886818,Human_miRNA_ID_1063497,Human_miRNA_ID_1074790,Human_miRNA_ID_2275388,Human_miRNA_ID_2401280,Human_miRNA_ID_2495206,Human_miRNA_ID_2501131,Human_miRNA_ID_3109163,Human_miRNA_ID_3110607 RMVar_hsa_circ_93931,RMVar_hsa_circ_101585,RMVar_hsa_circ_112795,RMVar_hsa_circ_104320,RMVar_hsa_circ_96869,RMVar_hsa_circ_157937,RMVar_hsa_circ_157939,RMVar_hsa_circ_157940,RMVar_hsa_circ_157941,RMVar_hsa_circ_157938 32273 RMVar_ID_32273 Human_SNP_ID_504474637 A-to-I Human chr12 - 64729111 64729111 64729111 GGGTGGGGGGAAGAGAACTTTAGTATAGGTAGAAAAGGAAAATGAGACCAGCTGTGTTCTAGATT GGGTGGGGGGAAGAGAACTTTAGTATAGGTAGGAAAGGAAAATGAGACCAGCTGTGTTCTAGATT T C GNS Ensembl:ENSG00000135677 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1160597605 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10926,RMVar_hsa_circ_93931,RMVar_hsa_circ_101585,RMVar_hsa_circ_104320,RMVar_hsa_circ_102714,RMVar_hsa_circ_157937,RMVar_hsa_circ_157939,RMVar_hsa_circ_157938,RMVar_hsa_circ_373071,RMVar_hsa_circ_157942,RMVar_hsa_circ_372119,RMVar_hsa_circ_113023,RMVar_hsa_circ_92124,RMVar_hsa_circ_157944,RMVar_hsa_circ_157946,RMVar_hsa_circ_157945,RMVar_hsa_circ_157943,RMVar_hsa_circ_85404,RMVar_hsa_circ_157947,RMVar_hsa_circ_157950,RMVar_hsa_circ_322918,RMVar_hsa_circ_366039,RMVar_hsa_circ_157948,RMVar_hsa_circ_378708,RMVar_hsa_circ_325213,RMVar_hsa_circ_51001,RMVar_hsa_circ_300911,RMVar_hsa_circ_157951,RMVar_hsa_circ_157952,RMVar_hsa_circ_157949 32274 RMVar_ID_32274 Human_SNP_ID_504475136 A-to-I Human chr12 - 64731350 64731350 64731350 AGCCTCGGCTGGGTGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAGGGCAGGCGG AGCCTCGGCTGGGTGCAGTGGCTCACGCCTGTGATCCCAGCACTTTGGGAGGCCAGGGCAGGCGG T C GNS Ensembl:ENSG00000135677 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1392326888 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10926,RMVar_hsa_circ_93931,RMVar_hsa_circ_101585,RMVar_hsa_circ_104320,RMVar_hsa_circ_102714,RMVar_hsa_circ_157937,RMVar_hsa_circ_157939,RMVar_hsa_circ_157938,RMVar_hsa_circ_373071,RMVar_hsa_circ_157942,RMVar_hsa_circ_372119,RMVar_hsa_circ_113023,RMVar_hsa_circ_92124,RMVar_hsa_circ_157944,RMVar_hsa_circ_157946,RMVar_hsa_circ_157945,RMVar_hsa_circ_157943,RMVar_hsa_circ_85404,RMVar_hsa_circ_157947,RMVar_hsa_circ_157950,RMVar_hsa_circ_322918,RMVar_hsa_circ_366039,RMVar_hsa_circ_157948,RMVar_hsa_circ_378708,RMVar_hsa_circ_325213,RMVar_hsa_circ_51001,RMVar_hsa_circ_300911,RMVar_hsa_circ_157951,RMVar_hsa_circ_157952,RMVar_hsa_circ_157949 32275 RMVar_ID_32275 Human_SNP_ID_504595066 A-to-I Human chr12 + 65244690 65244690 65244690 TAACATTCGGCTGGGCACAGTGGCTCACACCTATAATCCCAGTGCTTTGGGAAGCCGAGGTGGGT TAACATTCGGCTGGGCACAGTGGCTCACACCTGTAATCCCAGTGCTTTGGGAAGCCGAGGTGGGT A G LEMD3 Ensembl:ENSG00000174106 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs376194600 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4023 32276 RMVar_ID_32276 Human_SNP_ID_504628634 A-to-I Human chr12 + 65388688 65388688 65388688 GCCCAGGAGTTCAAGACCAGCCTGGGCAACATAGTGAGAACCCGTCTCTCCAAGAACATACAAAA GCCCAGGAGTTCAAGACCAGCCTGGGCAACATGGTGAGAACCCGTCTCTCCAAGAACATACAAAA A G MSRB3 Ensembl:ENSG00000174099 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs961805663 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9862,RMVar_hsa_circ_157979,RMVar_hsa_circ_104257 32277 RMVar_ID_32277 Human_SNP_ID_504808094 A-to-I Human chr12 - 66123259 66123259 66123259 GGGCATGGGGGCGCGCACCTGTAGTTCCAGCTACTCGGGAGGCTGAGGCAGGATAATTGCTTGAA GGGCATGGGGGCGCGCACCTGTAGTTCCAGCTGCTCGGGAGGCTGAGGCAGGATAATTGCTTGAA T C LLPH Ensembl:ENSG00000139233 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1038911818 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23570532 32278 RMVar_ID_32278 Human_SNP_ID_504808096 A-to-I Human chr12 - 66123263 66123263 66123263 AGCCGGGCATGGGGGCGCGCACCTGTAGTTCCAGCTACTCGGGAGGCTGAGGCAGGATAATTGCT AGCCGGGCATGGGGGCGCGCACCTGTAGTTCCTGCTACTCGGGAGGCTGAGGCAGGATAATTGCT T A LLPH Ensembl:ENSG00000139233 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs774656693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6209924,Human_RBP_ID_23570532 Human_miRNA_ID_171403 32279 RMVar_ID_32279 Human_SNP_ID_504808112 A-to-I Human chr12 - 66123312 66123312 66123312 TAGCCTGGCTAATACAGTGAAACCCCATCTCTACTAAAAATACAAAATTAGCCGGGCATGGGGGC TAGCCTGGCTAATACAGTGAAACCCCATCTCTGCTAAAAATACAAAATTAGCCGGGCATGGGGGC T C LLPH Ensembl:ENSG00000139233 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs752226142 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1219878 32280 RMVar_ID_32280 Human_SNP_ID_504808116 A-to-I Human chr12 - 66123323 66123323 66123323 CAGTTCGAGACTAGCCTGGCTAATACAGTGAAACCCCATCTCTACTAAAAATACAAAATTAGCCG CAGTTCGAGACTAGCCTGGCTAATACAGTGAAGCCCCATCTCTACTAAAAATACAAAATTAGCCG T C LLPH Ensembl:ENSG00000139233 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1421154846 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1476019,Human_RBP_ID_18263035 32281 RMVar_ID_32281 Human_SNP_ID_504808136 A-to-I Human chr12 - 66123389 66123389 66123389 TGGGCATGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGTGGATCACGAGG TGGGCATGGTGGCTCACACCTGTAATCCCAGCCCTTTGGGAGGCCGAGGCAGGTGGATCACGAGG T G LLPH Ensembl:ENSG00000139233 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1332501059 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_54429,Human_miRNA_ID_61987,Human_miRNA_ID_384675,Human_miRNA_ID_561249,Human_miRNA_ID_568683,Human_miRNA_ID_769295,Human_miRNA_ID_774192,Human_miRNA_ID_779016,Human_miRNA_ID_783895,Human_miRNA_ID_788725,Human_miRNA_ID_1105221,Human_miRNA_ID_1110025,Human_miRNA_ID_1510823,Human_miRNA_ID_1566187,Human_miRNA_ID_1571838,Human_miRNA_ID_1579021,Human_miRNA_ID_1586703,Human_miRNA_ID_1598385,Human_miRNA_ID_1607827,Human_miRNA_ID_1612739,Human_miRNA_ID_1620228,Human_miRNA_ID_1636349,Human_miRNA_ID_1641109,Human_miRNA_ID_1645438,Human_miRNA_ID_1650958 32282 RMVar_ID_32282 Human_SNP_ID_504814260 A-to-I Human chr12 - 66149249 66149249 66149249 TTTCGTAGAGAGGGGGTTTTGCTGTGTCACCCAGGCTGGTCTCAAACTCCTGGACTCAAGCAATC TTTCGTAGAGAGGGGGTTTTGCTGTGTCACCCGGGCTGGTCTCAAACTCCTGGACTCAAGCAATC T C TMBIM4,AC078927.1 Ensembl:ENSG00000155957,Ensembl:ENSG00000228144 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1016707815 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5887,RMVar_hsa_circ_157982,RMVar_hsa_circ_66181,RMVar_hsa_circ_30947,RMVar_hsa_circ_90614,RMVar_hsa_circ_271599,RMVar_hsa_circ_157983,RMVar_hsa_circ_157984,RMVar_hsa_circ_157985 32283 RMVar_ID_32283 Human_SNP_ID_504814807 A-to-I Human chr12 - 66151366 66151366 66151366 GGGCATGGTGGTGTGCACCTATAGTCCCAGCTACTTGGGAGGCTGAGGTGGGAGGATCACTGTAA GGGCATGGTGGTGTGCACCTATAGTCCCAGCTGCTTGGGAGGCTGAGGTGGGAGGATCACTGTAA T C TMBIM4,AC078927.1 Ensembl:ENSG00000155957,Ensembl:ENSG00000228144 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223760700 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5887,RMVar_hsa_circ_157982,RMVar_hsa_circ_66181,RMVar_hsa_circ_30947,RMVar_hsa_circ_90614,RMVar_hsa_circ_271599,RMVar_hsa_circ_157983,RMVar_hsa_circ_157984,RMVar_hsa_circ_157985 32284 RMVar_ID_32284 Human_SNP_ID_504834792 A-to-I Human chr12 + 66234416 66234416 66234416 GACTTTGCACCTGGTAGGCAGATACAGGAGATACAATATAGGGTGTAATAGAAGTTTGAGTGATC GACTTTGCACCTGGTAGGCAGATACAGGAGATGCAATATAGGGTGTAATAGAAGTTTGAGTGATC A G IRAK3 Ensembl:ENSG00000090376 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335742448 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265450,RMVar_hsa_circ_291287,RMVar_hsa_circ_311606,RMVar_hsa_circ_157995 32285 RMVar_ID_32285 Human_SNP_ID_504857263 A-to-I Human chr12 + 66326317 66326317 66326317 CAGGCTGGAGTGCAGTGGCGCGATCTTGGCTCACTGTAAGTTCCGCCTCCCAGGTTCAAGTGATT CAGGCTGGAGTGCAGTGGCGCGATCTTGGCTCGCTGTAAGTTCCGCCTCCCAGGTTCAAGTGATT A G HELB Ensembl:ENSG00000127311 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973999256 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_286794,RMVar_hsa_circ_157998,RMVar_hsa_circ_346233 32286 RMVar_ID_32286 Human_SNP_ID_504857434 A-to-I Human chr12 + 66326968 66326967 66326968 TGAGGCATGAGAATCACTTGATCCTGGGAGGCAGAGGTTGCAGCAAGCTGAGATTGTGCCACTGC TGAGGCATGAGAATCACTTGATCCTGGGAGGC_GAGGTTGCAGCAAGCTGAGATTGTGCCACTGC CA C HELB Ensembl:ENSG00000127311 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1338126144 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_286794,RMVar_hsa_circ_157998,RMVar_hsa_circ_346233 32287 RMVar_ID_32287 Human_SNP_ID_504861662 A-to-I Human chr12 + 66344640 66344640 66344640 AGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTATATGCATGTGCTACCATG AGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCCAGTAGCTGGGATTATATGCATGTGCTACCATG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs563943208 Functional Loss SNV dbSNP153 33..33 33 - - - 32288 RMVar_ID_32288 Human_SNP_ID_505010279 A-to-I Human chr12 - 66974048 66974047 66974048 TGTTGGCAGGCGCCTGTAATCCCCACCTACTCAGGAGGCTAGGGCAGGCAGAATGGCTTGAACCA TGTTGGCAGGCGCCTGTAATCCCCACCTACTC_GGAGGCTAGGGCAGGCAGAATGGCTTGAACCA CT C AC073530.1,GRIP1 Ensembl:ENSG00000257083,Ensembl:ENSG00000155974 lincRNA,Protein coding intron,intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1389993913 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_9697465 32289 RMVar_ID_32289 Human_SNP_ID_505094877 A-to-I Human chr12 + 67316958 67316958 67316958 TCACTTGAAGACAGGAGTTGGAGACCAGCTCTAGGCAACATAGTGAGACCCTGTCTCTACCAAAA TCACTTGAAGACAGGAGTTGGAGACCAGCTCTGGGCAACATAGTGAGACCCTGTCTCTACCAAAA A G CAND1 Ensembl:ENSG00000111530 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1290665088 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6212270 32290 RMVar_ID_32290 Human_SNP_ID_505095079 A-to-I Human chr12 + 67317587 67317587 67317587 TCACTGCAACCTCTGCCTCCCGGGTTCTAGCTATTCTCCTGCCTCAGCCTCCCAAGTAGCTGTGA TCACTGCAACCTCTGCCTCCCGGGTTCTAGCTGTTCTCCTGCCTCAGCCTCCCAAGTAGCTGTGA A G CAND1 Ensembl:ENSG00000111530 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs764548591 Functional Loss SNV dbSNP153 33..33 33 - - - 32291 RMVar_ID_32291 Human_SNP_ID_505095247 A-to-I Human chr12 + 67318264 67318264 67318264 GCATGCACCACTGCACTCCAGCCTGGGTGACAAAGCGAGACCCTGTCTCAAAAAAAACAAGGACT GCATGCACCACTGCACTCCAGCCTGGGTGACAGAGCGAGACCCTGTCTCAAAAAAAACAAGGACT A G CAND1 Ensembl:ENSG00000111530 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1214816492 Functional Loss SNV dbSNP153 33..33 33 - - - 32292 RMVar_ID_32292 Human_SNP_ID_505286815 A-to-I Human chr12 - 68143463 68143463 68143463 TGTCTGCCCCAACCAGCAGGACCTTCTTCAGTAGAATTCTCTCTCCACATGCAAGGTCTAGTCCG TGTCTGCCCCAACCAGCAGGACCTTCTTCAGTCGAATTCTCTCTCCACATGCAAGGTCTAGTCCG T G - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1350585591 Functional Loss SNV dbSNP153 33..33 33 - - - 32293 RMVar_ID_32293 Human_SNP_ID_505286816 A-to-I Human chr12 + 68143468 68143468 68143468 TAGACCTTGCATGTGGAGAGAGAATTCTACTGAAGAAGGTCCTGCTGGTTGGGGCAGACAACTTC TAGACCTTGCATGTGGAGAGAGAATTCTACTGGAGAAGGTCCTGCTGGTTGGGGCAGACAACTTC A G AC007458.1,IFNG-AS1 Ensembl:ENSG00000256708,Ensembl:ENSG00000255733 Pseudogene,lincRNA exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1325649842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4238932 32294 RMVar_ID_32294 Human_SNP_ID_505286830 A-to-I Human chr12 + 68143503 68143503 68143503 AAGGTCCTGCTGGTTGGGGCAGACAACTTCACACTGCTTGGCAAGCCACTCCTCAGAAAGGATCT AAGGTCCTGCTGGTTGGGGCAGACAACTTCACGCTGCTTGGCAAGCCACTCCTCAGAAAGGATCT A G AC007458.1,IFNG-AS1 Ensembl:ENSG00000256708,Ensembl:ENSG00000255733 Pseudogene,lincRNA exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs11555388 Functional Loss SNV dbSNP153 33..33 33 - - - 32295 RMVar_ID_32295 Human_SNP_ID_505286838 A-to-I Human chr12 + 68143525 68143525 68143525 ACAACTTCACACTGCTTGGCAAGCCACTCCTCAGAAAGGATCTTGTTTGAGTAGAAGCCATAGTC ACAACTTCACACTGCTTGGCAAGCCACTCCTCGGAAAGGATCTTGTTTGAGTAGAAGCCATAGTC A G AC007458.1,IFNG-AS1 Ensembl:ENSG00000256708,Ensembl:ENSG00000255733 Pseudogene,lincRNA exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1281102721 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6239442 32296 RMVar_ID_32296 Human_SNP_ID_505401780 A-to-I Human chr12 + 68613150 68613150 68613150 GCCGAGCCGAGGAAGGCGGATCATTTGAGGTGAAGAGTTCGAGAACAGCCTGGGCAACATGGTGA GCCGAGCCGAGGAAGGCGGATCATTTGAGGTGGAGAGTTCGAGAACAGCCTGGGCAACATGGTGA A G RAP1B Ensembl:ENSG00000127314 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1469171667 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6212860,Human_RBP_ID_12014022,Human_RBP_ID_24996534 32297 RMVar_ID_32297 Human_SNP_ID_505401805 A-to-I Human chr12 + 68613223 68613223 68613223 CTTTACTAAAAATACAAAACATAGCCGGGTGTAGTGGCACGCGCCTGCAATCCCAGCTATTCGGG CTTTACTAAAAATACAAAACATAGCCGGGTGTGGTGGCACGCGCCTGCAATCCCAGCTATTCGGG A G RAP1B Ensembl:ENSG00000127314 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs563168887 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6212861,Human_RBP_ID_12014031,Human_RBP_ID_24996537 32298 RMVar_ID_32298 Human_SNP_ID_505402826 A-to-I Human chr12 + 68616545 68616545 68616545 CTCAGCTCACTGCAACCTCCGCCTCCAGGTTCAAGCAGATCTCCTGCCTTAGCTAGTACTACAGG CTCAGCTCACTGCAACCTCCGCCTCCAGGTTCGAGCAGATCTCCTGCCTTAGCTAGTACTACAGG A G RAP1B Ensembl:ENSG00000127314 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1029547393 Functional Loss SNV dbSNP153 33..33 33 - - - 32299 RMVar_ID_32299 Human_SNP_ID_505402908 A-to-I Human chr12 + 68616775 68616775 68616775 ATTTTTTGTAGAGACGTTTCGCCATGTTGCCCAAGCTCACCTCAAACTCGTGGGCTCAAGGGATC ATTTTTTGTAGAGACGTTTCGCCATGTTGCCCGAGCTCACCTCAAACTCGTGGGCTCAAGGGATC A G RAP1B Ensembl:ENSG00000127314 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs868092434 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12014202 32300 RMVar_ID_32300 Human_SNP_ID_505403314 A-to-I Human chr12 + 68618162 68618162 68618162 CAGGCTAGAATGCAGTGGCACAATCTTCGCTCAGTGCAACCTCTGCTCCCAGGTTCAAGCAATTC CAGGCTAGAATGCAGTGGCACAATCTTCGCTCGGTGCAACCTCTGCTCCCAGGTTCAAGCAATTC A G RAP1B Ensembl:ENSG00000127314 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1226685109 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12014274 32301 RMVar_ID_32301 Human_SNP_ID_505403555 A-to-I Human chr12 + 68619087 68619087 68619087 GTGCCACTGCGCTTCAACCTGGGTGACAGAGCAAGACCCTGTCTCGAAAAACAAAACAAAAACAC GTGCCACTGCGCTTCAACCTGGGTGACAGAGCGAGACCCTGTCTCGAAAAACAAAACAAAAACAC A G RAP1B Ensembl:ENSG00000127314 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1440596096 Functional Loss SNV dbSNP153 33..33 33 - - - 32302 RMVar_ID_32302 Human_SNP_ID_505405006 A-to-I Human chr12 + 68624721 68624721 68624721 TCCTGTAGTCCCAGCTACTCGGGAGGCTGAGCAGGAGAATCGCTGGAACCTGGCAGGCAGAACTT TCCTGTAGTCCCAGCTACTCGGGAGGCTGAGCGGGAGAATCGCTGGAACCTGGCAGGCAGAACTT A G RAP1B Ensembl:ENSG00000127314 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs558117341 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12014607 Human_Splice_Rec_1395378,Human_Splice_Rec_1395410,Human_Splice_Rec_1395448,Human_Splice_Rec_1395504,Human_Splice_Rec_1395522,Human_Splice_Rec_1395606,Human_Splice_Rec_1395614,Human_Splice_Rec_1395634 32303 RMVar_ID_32303 Human_SNP_ID_505405890 A-to-I Human chr12 + 68627984 68627984 68627984 AAAAAATTTAATCAGGCATGCAGCACACGCCTATAGTCCAGTTACTCAGGATGTTGAGGTGGGTA AAAAAATTTAATCAGGCATGCAGCACACGCCTGTAGTCCAGTTACTCAGGATGTTGAGGTGGGTA A G RAP1B Ensembl:ENSG00000127314 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs147049030 Functional Loss SNV dbSNP153 33..33 33 - - - 32304 RMVar_ID_32304 Human_SNP_ID_505407217 A-to-I Human chr12 + 68632870 68632870 68632870 GCTAATGATTTTTTTAGAGATGATGCCTCACTATGTTGTCTAGGCTGGTCTGGAACTCCTGGCCC GCTAATGATTTTTTTAGAGATGATGCCTCACTGTGTTGTCTAGGCTGGTCTGGAACTCCTGGCCC A G RAP1B Ensembl:ENSG00000127314 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs762222259 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12014941 32305 RMVar_ID_32305 Human_SNP_ID_505410007 A-to-I Human chr12 - 68643002 68643002 68643002 CAGTGGACCGTGGGCAGCCAGGGTCGGTGAAGAATCCCAACATGGCTGGGCGAAAACTTGCTCTA CAGTGGACCGTGGGCAGCCAGGGTCGGTGAAGGATCCCAACATGGCTGGGCGAAAACTTGCTCTA T C - - Other Unknown GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs879053919 Functional Loss SNV dbSNP153 33..33 33 - - - 32306 RMVar_ID_32306 Human_SNP_ID_505410876 A-to-I Human chr12 + 68646365 68646365 68646365 TCACCGGGGCTGGAGTGCAGTGGCACGATCTCAGCTTACTGCAACCTCCACTTCTCGGGTTCACT TCACCGGGGCTGGAGTGCAGTGGCACGATCTCGGCTTACTGCAACCTCCACTTCTCGGGTTCACT A G RAP1B Ensembl:ENSG00000127314 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs544756015 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12070245 32307 RMVar_ID_32307 Human_SNP_ID_505410920 A-to-I Human chr12 + 68646498 68646498 68646498 TTGTACTTTTAGTAGAAACGGGGTTTCACCATATTGGCCAGGCTGAACTCCTGACCTTGTGATCC TTGTACTTTTAGTAGAAACGGGGTTTCACCATGTTGGCCAGGCTGAACTCCTGACCTTGTGATCC A G RAP1B Ensembl:ENSG00000127314 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs997683387 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12015437 32308 RMVar_ID_32308 Human_SNP_ID_505411265 A-to-I Human chr12 + 68647501 68647498 68647501 CCTCAGCCTCCCAAAGTGCTGGGATTACAGACATGAGCCACCACATCTGGCCGAGTTCTTGATTA CCTCAGCCTCCCAAAGTGCTGGGATTACAG___TGAGCCACCACATCTGGCCGAGTTCTTGATTA GACA G RAP1B Ensembl:ENSG00000127314 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1302958238 Functional Loss DEL dbSNP153 31..33 33 - - - 32309 RMVar_ID_32309 Human_SNP_ID_505411729 A-to-I Human chr12 + 68649246 68649246 68649246 TTTAAAATTTTTTGTAGAGATGGCGTCTTGCTATATTGCTTAGGCTGGTCTTAAACTCCTGGCCT TTTAAAATTTTTTGTAGAGATGGCGTCTTGCTCTATTGCTTAGGCTGGTCTTAAACTCCTGGCCT A C RAP1B Ensembl:ENSG00000127314 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs562099157 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8934,RMVar_hsa_circ_112832,RMVar_hsa_circ_291654,RMVar_hsa_circ_329644,RMVar_hsa_circ_38970,RMVar_hsa_circ_158071,RMVar_hsa_circ_158072 32310 RMVar_ID_32310 Human_SNP_ID_505411730 A-to-I Human chr12 + 68649246 68649246 68649246 TTTAAAATTTTTTGTAGAGATGGCGTCTTGCTATATTGCTTAGGCTGGTCTTAAACTCCTGGCCT TTTAAAATTTTTTGTAGAGATGGCGTCTTGCTGTATTGCTTAGGCTGGTCTTAAACTCCTGGCCT A G RAP1B Ensembl:ENSG00000127314 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs562099157 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8934,RMVar_hsa_circ_112832,RMVar_hsa_circ_291654,RMVar_hsa_circ_329644,RMVar_hsa_circ_38970,RMVar_hsa_circ_158071,RMVar_hsa_circ_158072 32311 RMVar_ID_32311 Human_SNP_ID_505426374 A-to-I Human chr12 + 68708780 68708780 68708780 AGCTGGGATTACAGGCTTGCGTCACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGATGTGGA AGCTGGGATTACAGGCTTGCGTCACCACGCCCCGCTAATTTTTGTATTTTTAGTAGAGATGTGGA A C NUP107 Ensembl:ENSG00000111581 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1000202838 Functional Loss SNV dbSNP153 33..33 33 - - - 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_158091,RMVar_hsa_circ_124202,RMVar_hsa_circ_324554,RMVar_hsa_circ_328440,RMVar_hsa_circ_158092,RMVar_hsa_circ_158090 32312 RMVar_ID_32312 Human_SNP_ID_505431768 A-to-I Human chr12 + 68730859 68730859 68730859 GGGCATAGTGGCATGTGCCTGTAGTCCCACCTACCCGGGAGGTTGAGGTGGGAGGATCACCTGAG GGGCATAGTGGCATGTGCCTGTAGTCCCACCTGCCCGGGAGGTTGAGGTGGGAGGATCACCTGAG A G NUP107 Ensembl:ENSG00000111581 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941434373 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_330656,RMVar_hsa_circ_158085,RMVar_hsa_circ_75408,RMVar_hsa_circ_20227,RMVar_hsa_circ_158104,RMVar_hsa_circ_8479,RMVar_hsa_circ_313720,RMVar_hsa_circ_346192,RMVar_hsa_circ_349931,RMVar_hsa_circ_321896,RMVar_hsa_circ_279616,RMVar_hsa_circ_158106,RMVar_hsa_circ_158107,RMVar_hsa_circ_158108,RMVar_hsa_circ_158105,RMVar_hsa_circ_158103,RMVar_hsa_circ_306837,RMVar_hsa_circ_83618,RMVar_hsa_circ_158109,RMVar_hsa_circ_158110,RMVar_hsa_circ_378959,RMVar_hsa_circ_114359,RMVar_hsa_circ_314920,RMVar_hsa_circ_158114,RMVar_hsa_circ_316688,RMVar_hsa_circ_158118,RMVar_hsa_circ_109020,RMVar_hsa_circ_158117,RMVar_hsa_circ_298387,RMVar_hsa_circ_158119 32313 RMVar_ID_32313 Human_SNP_ID_505433125 A-to-I Human chr12 + 68736453 68736453 68736453 CTTTTTTTGTTTTAGAGACAAGGTCTTGCTCTATCACCCAGGCTGGAGGACAGTGGCTTCATCAT CTTTTTTTGTTTTAGAGACAAGGTCTTGCTCTGTCACCCAGGCTGGAGGACAGTGGCTTCATCAT A G NUP107 Ensembl:ENSG00000111581 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1565704694 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12016526 RMVar_hsa_circ_321896,RMVar_hsa_circ_158107,RMVar_hsa_circ_158108,RMVar_hsa_circ_114359,RMVar_hsa_circ_158118,RMVar_hsa_circ_266053,RMVar_hsa_circ_378186,RMVar_hsa_circ_76220,RMVar_hsa_circ_158122,RMVar_hsa_circ_158123 32314 RMVar_ID_32314 Human_SNP_ID_505434413 A-to-I Human chr12 + 68741844 68741844 68741844 GGATGCCAAAGAAGACCATGAAAGAACACATCAAATGGTCTTACTGAGAAAGCTTTGTCTGCCAA GGATGCCAAAGAAGACCATGAAAGAACACATCGAATGGTCTTACTGAGAAAGCTTTGTCTGCCAA A G NUP107 Ensembl:ENSG00000111581 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs17854284 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1800035,Human_RBP_ID_3412541,Human_RBP_ID_12016566,Human_RBP_ID_18160540,Human_RBP_ID_22645156,Human_RBP_ID_23571915 Human_Splice_Rec_1395716,Human_Splice_Rec_1395774,Human_Splice_Rec_1395848,Human_Splice_Rec_1395902 Human_miRNA_ID_1726939 RMVar_hsa_circ_321896,RMVar_hsa_circ_158107,RMVar_hsa_circ_158108,RMVar_hsa_circ_114359,RMVar_hsa_circ_158118,RMVar_hsa_circ_266053,RMVar_hsa_circ_378186,RMVar_hsa_circ_76220,RMVar_hsa_circ_158122,RMVar_hsa_circ_158123 32315 RMVar_ID_32315 Human_SNP_ID_505439092 A-to-I Human chr12 + 68760090 68760089 68760090 GGCCGGGTGCCATGGCTCACGCCTGTAATTCCAACACTGTGGGAGGCCGAGGCAGGAGGATCGCT GGCCGGGTGCCATGGCTCACGCCTGTAATTCC_ACACTGTGGGAGGCCGAGGCAGGAGGATCGCT CA C SLC35E3 Ensembl:ENSG00000175782 Protein coding intron GSE47997;GSE38233;GSE107867 K562 cells&HepG2 cells;cultured B-cells;ASD brains,Fragile X samples from NIH NeuroBioBank - 23474544,24183664,30559470 RNA-Seq:(High) rs140721623 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_24997494 Human_Splice_Rec_1395968 32316 RMVar_ID_32316 Human_SNP_ID_505439467 A-to-I Human chr12 + 68761984 68761983 68761985 GGGGAGTATTTTGTTGTTGTTGTTTTTGAGACAGGGTCTTGCTCTGTCACCCAGGCTGGAGTGAA GGGGAGTATTTTGTTGTTGTTGTTTTTGAGAC__GGTCTTGCTCTGTCACCCAGGCTGGAGTGAA CAG C SLC35E3 Ensembl:ENSG00000175782 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1416155849 Functional Loss DEL dbSNP153 33..34 33 - - - 32317 RMVar_ID_32317 Human_SNP_ID_505439491 A-to-I Human chr12 + 68762078 68762078 68762078 AAACTGTTGGGCTCAAGCATTCTTCCCACCTCAGCCTTCCAAAGTGCTGGGATTACAGGTGTGAG AAACTGTTGGGCTCAAGCATTCTTCCCACCTCGGCCTTCCAAAGTGCTGGGATTACAGGTGTGAG A G SLC35E3 Ensembl:ENSG00000175782 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs986414762 Functional Loss SNV dbSNP153 33..33 33 - - - 32318 RMVar_ID_32318 Human_SNP_ID_505439811 A-to-I Human chr12 + 68763531 68763531 68763531 CCTGCCTCAGCCTCCCGAGTAGCCGGTATTACAGGCATGCACCACCACGCCCGGCTAATTTTGTA CCTGCCTCAGCCTCCCGAGTAGCCGGTATTACGGGCATGCACCACCACGCCCGGCTAATTTTGTA A G SLC35E3 Ensembl:ENSG00000175782 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1015788030 Functional Loss SNV dbSNP153 33..33 33 - - - 32319 RMVar_ID_32319 Human_SNP_ID_505440186 A-to-I Human chr12 + 68765103 68765103 68765103 ACATGGAGAAACCCTGTCTCAACTAATAATACAAAATTAGCCAGGCGTGGTGGCGCATGCCTGTA ACATGGAGAAACCCTGTCTCAACTAATAATACGAAATTAGCCAGGCGTGGTGGCGCATGCCTGTA A G SLC35E3 Ensembl:ENSG00000175782 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs889607498 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17825610 32320 RMVar_ID_32320 Human_SNP_ID_505440188 A-to-I Human chr12 + 68765113 68765113 68765113 ACCCTGTCTCAACTAATAATACAAAATTAGCCAGGCGTGGTGGCGCATGCCTGTAATCCCAGCTA ACCCTGTCTCAACTAATAATACAAAATTAGCCGGGCGTGGTGGCGCATGCCTGTAATCCCAGCTA A G SLC35E3 Ensembl:ENSG00000175782 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs982457858 Functional Loss SNV dbSNP153 33..33 33 - - - 32321 RMVar_ID_32321 Human_SNP_ID_505440206 A-to-I Human chr12 + 68765167 68765167 68765167 AATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCCGGGAGGCGGCGGTTGCAGT AATCCCAGCTACTCGGGAGGCTGAGGCAGGAGCATCACTTGAACCCGGGAGGCGGCGGTTGCAGT A C SLC35E3 Ensembl:ENSG00000175782 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1450246085 Functional Loss SNV dbSNP153 33..33 33 - - - 32322 RMVar_ID_32322 Human_SNP_ID_505440357 A-to-I Human chr12 + 68765632 68765632 68765632 ATATATATATGTGTGTGTGTGTATATATATATATATGTGTGTGTGTGTGTGTGTATACATATATA ATATATATATGTGTGTGTGTGTATATATATATGTATGTGTGTGTGTGTGTGTGTATACATATATA A G SLC35E3 Ensembl:ENSG00000175782 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1341417947 Functional Loss SNV dbSNP153 33..33 33 - - - 32323 RMVar_ID_32323 Human_SNP_ID_505440384 A-to-I Human chr12 + 68765664 68765655 68765665 ATATGTGTGTGTGTGTGTGTGTATACATATATACACATATATACACACACACATACATATACATG ATATGTGTGTGTGTGTGTGTGTAT__________ACATATATACACACACACATACATATACATG TACATATATAC T SLC35E3 Ensembl:ENSG00000175782 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1452358849 Functional Loss DEL dbSNP153 25..34 33 - - - 32324 RMVar_ID_32324 Human_SNP_ID_505440388 A-to-I Human chr12 + 68765670 68765667 68765671 GTGTGTGTGTGTGTGTATACATATATACACATATATACACACACACATACATATACATGTGTATA GTGTGTGTGTGTGTGTATACATATATACAC____ATACACACACACATACATATACATGTGTATA CATAT C SLC35E3 Ensembl:ENSG00000175782 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037779209 Functional Loss DEL dbSNP153 31..34 33 - - - 32325 RMVar_ID_32325 Human_SNP_ID_505440389 A-to-I Human chr12 + 68765670 68765667 68765671 GTGTGTGTGTGTGTGTATACATATATACACATATATACACACACACATACATATACATGTGTATA GTGTGTGTGTGTGTGTATACATATATACACAT__ATACACACACACATACATATACATGTGTATA CATAT CAT SLC35E3 Ensembl:ENSG00000175782 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037779209 Functional Loss DEL dbSNP153 33..34 33 - - - 32326 RMVar_ID_32326 Human_SNP_ID_505440390 A-to-I Human chr12 + 68765668 68765668 68765668 GTGTGTGTGTGTGTGTGTATACATATATACACATATATACACACACACATACATATACATGTGTA GTGTGTGTGTGTGTGTGTATACATATATACACCTATATACACACACACATACATATACATGTGTA A C SLC35E3 Ensembl:ENSG00000175782 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs372783294 Functional Loss SNV dbSNP153 33..33 33 - - - 32327 RMVar_ID_32327 Human_SNP_ID_505440396 A-to-I Human chr12 + 68765674 68765674 68765674 GTGTGTGTGTGTATACATATATACACATATATACACACACACATACATATACATGTGTATATATA GTGTGTGTGTGTATACATATATACACATATATGCACACACACATACATATACATGTGTATATATA A G SLC35E3 Ensembl:ENSG00000175782 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs929851495 Functional Loss SNV dbSNP153 33..33 33 - - - 32328 RMVar_ID_32328 Human_SNP_ID_505440546 A-to-I Human chr12 + 68766285 68766285 68766285 GAGGCAGGCAGATCACCTGAGGTTGGGAGTTCAAGACCAGTCTGACCAACATGGAGGAATCCCGT GAGGCAGGCAGATCACCTGAGGTTGGGAGTTCGAGACCAGTCTGACCAACATGGAGGAATCCCGT A G SLC35E3 Ensembl:ENSG00000175782 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs917727711 Functional Loss SNV dbSNP153 33..33 33 - - - 32329 RMVar_ID_32329 Human_SNP_ID_505440559 A-to-I Human chr12 + 68766325 68766325 68766325 TCTGACCAACATGGAGGAATCCCGTCTCTACTAAAAATACAAAATTAGCCAGGCATGGTGGCACA TCTGACCAACATGGAGGAATCCCGTCTCTACTGAAAATACAAAATTAGCCAGGCATGGTGGCACA A G SLC35E3 Ensembl:ENSG00000175782 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs936579997 Functional Loss SNV dbSNP153 33..33 33 - - - 32330 RMVar_ID_32330 Human_SNP_ID_505440642 A-to-I Human chr12 + 68766670 68766670 68766670 GCAGTGGCACAATCATGGCTCACTGCAGCCTCAGCCTCCTGGGCTCAAGCAATCCTCCTGCCTCA GCAGTGGCACAATCATGGCTCACTGCAGCCTCGGCCTCCTGGGCTCAAGCAATCCTCCTGCCTCA A G SLC35E3 Ensembl:ENSG00000175782 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs973605134 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1395978 32331 RMVar_ID_32331 Human_SNP_ID_505440671 A-to-I Human chr12 + 68766757 68766757 68766757 CAGGTGCACACCAACATACCTGGCTGATTTTTATATTTTTTGTAGAGACAGAGTTTTGCCATGTT CAGGTGCACACCAACATACCTGGCTGATTTTTGTATTTTTTGTAGAGACAGAGTTTTGCCATGTT A G SLC35E3 Ensembl:ENSG00000175782 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1001159878 Functional Loss SNV dbSNP153 33..33 33 - - - 32332 RMVar_ID_32332 Human_SNP_ID_505440673 A-to-I Human chr12 + 68766768 68766768 68766768 CAACATACCTGGCTGATTTTTATATTTTTTGTAGAGACAGAGTTTTGCCATGTTGCTCAGGCTGA CAACATACCTGGCTGATTTTTATATTTTTTGTTGAGACAGAGTTTTGCCATGTTGCTCAGGCTGA A T SLC35E3 Ensembl:ENSG00000175782 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053631733 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17561193 32333 RMVar_ID_32333 Human_SNP_ID_505440679 A-to-I Human chr12 + 68766774 68766773 68766775 ACCTGGCTGATTTTTATATTTTTTGTAGAGACAGAGTTTTGCCATGTTGCTCAGGCTGATCTCAA ACCTGGCTGATTTTTATATTTTTTGTAGAGAC__AGTTTTGCCATGTTGCTCAGGCTGATCTCAA CAG C SLC35E3 Ensembl:ENSG00000175782 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1455037227 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_17561193 32334 RMVar_ID_32334 Human_SNP_ID_505440687 A-to-I Human chr12 + 68766794 68766794 68766794 TTTTGTAGAGACAGAGTTTTGCCATGTTGCTCAGGCTGATCTCAAACTCTTGAGCTCAAGCCATC TTTTGTAGAGACAGAGTTTTGCCATGTTGCTCCGGCTGATCTCAAACTCTTGAGCTCAAGCCATC A C SLC35E3 Ensembl:ENSG00000175782 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355133032 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17561193 32335 RMVar_ID_32335 Human_SNP_ID_505440828 A-to-I Human chr12 + 68767410 68767410 68767410 CTAGTGGCACGTGCCTGTAGCTCCATCTACTCAGGAGGCTGAGGTGGGAGGATTGCTTGAGCCCA CTAGTGGCACGTGCCTGTAGCTCCATCTACTCGGGAGGCTGAGGTGGGAGGATTGCTTGAGCCCA A G SLC35E3 Ensembl:ENSG00000175782 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs947937366 Functional Loss SNV dbSNP153 33..33 33 - - - 32336 RMVar_ID_32336 Human_SNP_ID_505440834 A-to-I Human chr12 + 68767442 68767442 68767442 AGGAGGCTGAGGTGGGAGGATTGCTTGAGCCCAGAAGATGCAGGTTGCAGTGAGCCGAGATCATG AGGAGGCTGAGGTGGGAGGATTGCTTGAGCCCCGAAGATGCAGGTTGCAGTGAGCCGAGATCATG A C SLC35E3 Ensembl:ENSG00000175782 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1176824779 Functional Loss SNV dbSNP153 33..33 33 - - - 32337 RMVar_ID_32337 Human_SNP_ID_505440970 A-to-I Human chr12 + 68767990 68767990 68767990 ACTGAGAACAGCTGAGTTTATTTGTGCCATTTAGAAATTCGTAACTGTAGGCTGGGCGCAGTGGC ACTGAGAACAGCTGAGTTTATTTGTGCCATTTGGAAATTCGTAACTGTAGGCTGGGCGCAGTGGC A G SLC35E3 Ensembl:ENSG00000175782 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350687574 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12017104 32338 RMVar_ID_32338 Human_SNP_ID_505443862 A-to-I Human chr12 + 68779857 68779851 68779857 CTACTTGGGAAGATGAGGCAGAGGATTGCCTGAGCCCAGGAGTTTGAGGTTATAGTGAGCCATGA CTACTTGGGAAGATGAGGCAGAGGATT______GCCCAGGAGTTTGAGGTTATAGTGAGCCATGA TGCCTGA T SLC35E3 Ensembl:ENSG00000175782 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1461571913 Functional Loss DEL dbSNP153 28..33 33 - - - 32339 RMVar_ID_32339 Human_SNP_ID_505452529 A-to-I Human chr12 + 68815711 68815711 68815711 GGGATCTGCTTACCTCGGCCTCCTAAAGTGCTAGATTTACAGGTGTGAGCCACTGTGCCCAACGC GGGATCTGCTTACCTCGGCCTCCTAAAGTGCTGGATTTACAGGTGTGAGCCACTGTGCCCAACGC A G MDM2 Ensembl:ENSG00000135679 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1415774410 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12017663,Human_RBP_ID_19058673,Human_RBP_ID_24997656 Human_Splice_Rec_1396144,Human_Splice_Rec_1396145 RMVar_hsa_circ_118742,RMVar_hsa_circ_21562,RMVar_hsa_circ_38758,RMVar_hsa_circ_358206,RMVar_hsa_circ_158126,RMVar_hsa_circ_50736,RMVar_hsa_circ_295547,RMVar_hsa_circ_368986 32340 RMVar_ID_32340 Human_SNP_ID_505453090 A-to-I Human chr12 + 68817897 68817897 68817897 TTGGCTCACTGCAACCTCCGTCTCCTGGGTTCAAGTGATTCTCCTGCCTCGGCTTCCCGAGTAGC TTGGCTCACTGCAACCTCCGTCTCCTGGGTTCGAGTGATTCTCCTGCCTCGGCTTCCCGAGTAGC A G MDM2 Ensembl:ENSG00000135679 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1304592295 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3503,RMVar_hsa_circ_118742,RMVar_hsa_circ_21562,RMVar_hsa_circ_38758,RMVar_hsa_circ_358206,RMVar_hsa_circ_158126,RMVar_hsa_circ_50736,RMVar_hsa_circ_368986,RMVar_hsa_circ_274300,RMVar_hsa_circ_283432,RMVar_hsa_circ_325227,RMVar_hsa_circ_158128,RMVar_hsa_circ_158129 32341 RMVar_ID_32341 Human_SNP_ID_505453119 A-to-I Human chr12 + 68818022 68818022 68818022 CACGATGTTGACCAGGCTGGTCTTGAGCTCCTAACCTTCGGTAATCCACCTGCCATGGCCTCCCA CACGATGTTGACCAGGCTGGTCTTGAGCTCCTCACCTTCGGTAATCCACCTGCCATGGCCTCCCA A C MDM2 Ensembl:ENSG00000135679 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs773408815 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12017749,Human_RBP_ID_17561195,Human_RBP_ID_23159058 RMVar_hsa_circ_3503,RMVar_hsa_circ_118742,RMVar_hsa_circ_21562,RMVar_hsa_circ_38758,RMVar_hsa_circ_358206,RMVar_hsa_circ_158126,RMVar_hsa_circ_50736,RMVar_hsa_circ_368986,RMVar_hsa_circ_274300,RMVar_hsa_circ_283432,RMVar_hsa_circ_325227,RMVar_hsa_circ_158128,RMVar_hsa_circ_158129 32342 RMVar_ID_32342 Human_SNP_ID_505453120 A-to-I Human chr12 + 68818022 68818022 68818022 CACGATGTTGACCAGGCTGGTCTTGAGCTCCTAACCTTCGGTAATCCACCTGCCATGGCCTCCCA CACGATGTTGACCAGGCTGGTCTTGAGCTCCTGACCTTCGGTAATCCACCTGCCATGGCCTCCCA A G MDM2 Ensembl:ENSG00000135679 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs773408815 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12017749,Human_RBP_ID_17561195,Human_RBP_ID_23159058 RMVar_hsa_circ_3503,RMVar_hsa_circ_118742,RMVar_hsa_circ_21562,RMVar_hsa_circ_38758,RMVar_hsa_circ_358206,RMVar_hsa_circ_158126,RMVar_hsa_circ_50736,RMVar_hsa_circ_368986,RMVar_hsa_circ_274300,RMVar_hsa_circ_283432,RMVar_hsa_circ_325227,RMVar_hsa_circ_158128,RMVar_hsa_circ_158129 32343 RMVar_ID_32343 Human_SNP_ID_505453128 A-to-I Human chr12 + 68818044 68818044 68818044 TTGAGCTCCTAACCTTCGGTAATCCACCTGCCATGGCCTCCCAAAGTGCTGGGATTACAGATGTG TTGAGCTCCTAACCTTCGGTAATCCACCTGCCGTGGCCTCCCAAAGTGCTGGGATTACAGATGTG A G MDM2 Ensembl:ENSG00000135679 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs930876678 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17561195,Human_RBP_ID_23159058,Human_RBP_ID_24997696 RMVar_hsa_circ_3503,RMVar_hsa_circ_118742,RMVar_hsa_circ_21562,RMVar_hsa_circ_38758,RMVar_hsa_circ_358206,RMVar_hsa_circ_158126,RMVar_hsa_circ_50736,RMVar_hsa_circ_368986,RMVar_hsa_circ_274300,RMVar_hsa_circ_283432,RMVar_hsa_circ_325227,RMVar_hsa_circ_158128,RMVar_hsa_circ_158129 32344 RMVar_ID_32344 Human_SNP_ID_505453874 A-to-I Human chr12 + 68821147 68821147 68821147 TCGACTCACTGCAACCTCCGCCTCCCAGGTTCAAGCAATTCTTCTGCCTCAGCCTCCCGAGTAGA TCGACTCACTGCAACCTCCGCCTCCCAGGTTCCAGCAATTCTTCTGCCTCAGCCTCCCGAGTAGA A C MDM2 Ensembl:ENSG00000135679 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs562555186 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25026541 RMVar_hsa_circ_3503,RMVar_hsa_circ_118742,RMVar_hsa_circ_38758,RMVar_hsa_circ_158126,RMVar_hsa_circ_50736,RMVar_hsa_circ_368986,RMVar_hsa_circ_274300,RMVar_hsa_circ_283432,RMVar_hsa_circ_158130,RMVar_hsa_circ_158128,RMVar_hsa_circ_158129,RMVar_hsa_circ_271273,RMVar_hsa_circ_311091,RMVar_hsa_circ_360939,RMVar_hsa_circ_158131 32345 RMVar_ID_32345 Human_SNP_ID_505453922 A-to-I Human chr12 + 68821306 68821306 68821306 CTGACCTTGTGATCTGCCTGCCTCGGCCTTCCAAAGTCCTGGGATTACAGGTATGAGCCACTGCA CTGACCTTGTGATCTGCCTGCCTCGGCCTTCCGAAGTCCTGGGATTACAGGTATGAGCCACTGCA A G MDM2 Ensembl:ENSG00000135679 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968373910 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12017899,Human_RBP_ID_17561196 RMVar_hsa_circ_3503,RMVar_hsa_circ_118742,RMVar_hsa_circ_38758,RMVar_hsa_circ_158126,RMVar_hsa_circ_50736,RMVar_hsa_circ_368986,RMVar_hsa_circ_274300,RMVar_hsa_circ_283432,RMVar_hsa_circ_158130,RMVar_hsa_circ_158128,RMVar_hsa_circ_158129,RMVar_hsa_circ_271273,RMVar_hsa_circ_311091,RMVar_hsa_circ_360939,RMVar_hsa_circ_158131 32346 RMVar_ID_32346 Human_SNP_ID_505453962 A-to-I Human chr12 + 68821465 68821465 68821465 TGCTCTTAGGCCAGGTGTGATGGCTCATGCCTATAATTCCAGCACTTTAGGAGGCTAAGGCAGGA TGCTCTTAGGCCAGGTGTGATGGCTCATGCCTGTAATTCCAGCACTTTAGGAGGCTAAGGCAGGA A G MDM2 Ensembl:ENSG00000135679 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1565737203 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17561198 RMVar_hsa_circ_3503,RMVar_hsa_circ_118742,RMVar_hsa_circ_38758,RMVar_hsa_circ_158126,RMVar_hsa_circ_50736,RMVar_hsa_circ_368986,RMVar_hsa_circ_274300,RMVar_hsa_circ_283432,RMVar_hsa_circ_158130,RMVar_hsa_circ_158128,RMVar_hsa_circ_158129,RMVar_hsa_circ_271273,RMVar_hsa_circ_311091,RMVar_hsa_circ_360939,RMVar_hsa_circ_158131 32347 RMVar_ID_32347 Human_SNP_ID_505453997 A-to-I Human chr12 + 68821586 68821586 68821586 CTCTGCAAAAACTACAAAAATCAGCTTGGTATAGTGGTGCATGCCTGTAGTCCTAGCTACTCAGG CTCTGCAAAAACTACAAAAATCAGCTTGGTATGGTGGTGCATGCCTGTAGTCCTAGCTACTCAGG A G MDM2 Ensembl:ENSG00000135679 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs985587779 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25026542 RMVar_hsa_circ_3503,RMVar_hsa_circ_118742,RMVar_hsa_circ_38758,RMVar_hsa_circ_158126,RMVar_hsa_circ_50736,RMVar_hsa_circ_368986,RMVar_hsa_circ_274300,RMVar_hsa_circ_283432,RMVar_hsa_circ_158130,RMVar_hsa_circ_158128,RMVar_hsa_circ_158129,RMVar_hsa_circ_271273,RMVar_hsa_circ_311091,RMVar_hsa_circ_360939,RMVar_hsa_circ_158131 32348 RMVar_ID_32348 Human_SNP_ID_505454003 A-to-I Human chr12 + 68821602 68821602 68821602 AAAATCAGCTTGGTATAGTGGTGCATGCCTGTAGTCCTAGCTACTCAGGAGGCTGAGGCAGGAGG AAAATCAGCTTGGTATAGTGGTGCATGCCTGTGGTCCTAGCTACTCAGGAGGCTGAGGCAGGAGG A G MDM2 Ensembl:ENSG00000135679 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs148463923 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17561200 RMVar_hsa_circ_3503,RMVar_hsa_circ_118742,RMVar_hsa_circ_38758,RMVar_hsa_circ_158126,RMVar_hsa_circ_50736,RMVar_hsa_circ_368986,RMVar_hsa_circ_274300,RMVar_hsa_circ_283432,RMVar_hsa_circ_158130,RMVar_hsa_circ_158128,RMVar_hsa_circ_158129,RMVar_hsa_circ_271273,RMVar_hsa_circ_311091,RMVar_hsa_circ_360939,RMVar_hsa_circ_158131 32349 RMVar_ID_32349 Human_SNP_ID_505454012 A-to-I Human chr12 + 68821656 68821656 68821656 GAGGCAGGAGGATTTTTTGAGGCTGGGAGGTCAGGACTGTAGTGAACTGTGATCATGCCATCCAG GAGGCAGGAGGATTTTTTGAGGCTGGGAGGTCGGGACTGTAGTGAACTGTGATCATGCCATCCAG A G MDM2 Ensembl:ENSG00000135679 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs975671547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_811021,Human_RBP_ID_6213927,Human_RBP_ID_12017908,Human_RBP_ID_17561200,Human_RBP_ID_22795191 RMVar_hsa_circ_3503,RMVar_hsa_circ_118742,RMVar_hsa_circ_38758,RMVar_hsa_circ_158126,RMVar_hsa_circ_50736,RMVar_hsa_circ_368986,RMVar_hsa_circ_274300,RMVar_hsa_circ_283432,RMVar_hsa_circ_158130,RMVar_hsa_circ_158128,RMVar_hsa_circ_158129,RMVar_hsa_circ_271273,RMVar_hsa_circ_311091,RMVar_hsa_circ_360939,RMVar_hsa_circ_158131 32350 RMVar_ID_32350 Human_SNP_ID_505454105 A-to-I Human chr12 + 68822069 68822069 68822069 GGTAGAGACGGTGTTGCTATGTTGCCCAGGCTAGTCTTGACCTGAGCTCAAGAGATATTCTCACC GGTAGAGACGGTGTTGCTATGTTGCCCAGGCTGGTCTTGACCTGAGCTCAAGAGATATTCTCACC A G MDM2 Ensembl:ENSG00000135679 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1565737466 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1476480,Human_RBP_ID_12017928,Human_RBP_ID_17561202 RMVar_hsa_circ_3503,RMVar_hsa_circ_118742,RMVar_hsa_circ_38758,RMVar_hsa_circ_158126,RMVar_hsa_circ_50736,RMVar_hsa_circ_368986,RMVar_hsa_circ_274300,RMVar_hsa_circ_283432,RMVar_hsa_circ_158130,RMVar_hsa_circ_158128,RMVar_hsa_circ_158129,RMVar_hsa_circ_271273,RMVar_hsa_circ_311091,RMVar_hsa_circ_360939,RMVar_hsa_circ_158131 32351 RMVar_ID_32351 Human_SNP_ID_505456371 A-to-I Human chr12 + 68830775 68830775 68830775 CAGGCTGGAGTGCAGTGGTGCAATCTTGGCTCACTGCAACCTCCACCTCCCCGGTTCAGGCGATT CAGGCTGGAGTGCAGTGGTGCAATCTTGGCTCTCTGCAACCTCCACCTCCCCGGTTCAGGCGATT A T MDM2 Ensembl:ENSG00000135679 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs113583896 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3503,RMVar_hsa_circ_118742,RMVar_hsa_circ_38758,RMVar_hsa_circ_158126,RMVar_hsa_circ_28606,RMVar_hsa_circ_360939,RMVar_hsa_circ_36682,RMVar_hsa_circ_268768,RMVar_hsa_circ_285716,RMVar_hsa_circ_158135,RMVar_hsa_circ_158136 32352 RMVar_ID_32352 Human_SNP_ID_505456392 A-to-I Human chr12 + 68830884 68830884 68830884 CACCACACCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACTATGTTGGCCAGGCTGG CACCACACCTGGCTAATTTTTGTATTTTTAGTTGAGATGGGGTTTCACTATGTTGGCCAGGCTGG A T MDM2 Ensembl:ENSG00000135679 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1483199496 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3503,RMVar_hsa_circ_118742,RMVar_hsa_circ_38758,RMVar_hsa_circ_158126,RMVar_hsa_circ_28606,RMVar_hsa_circ_360939,RMVar_hsa_circ_36682,RMVar_hsa_circ_268768,RMVar_hsa_circ_285716,RMVar_hsa_circ_158135,RMVar_hsa_circ_158136 32353 RMVar_ID_32353 Human_SNP_ID_505456808 A-to-I Human chr12 + 68832532 68832532 68832532 GCTTAAAAAAATATATATTTTTTAAATTTTTGAGACAGTCTCTCACTCCGTTGCCCAGGCGGGAG GCTTAAAAAAATATATATTTTTTAAATTTTTGGGACAGTCTCTCACTCCGTTGCCCAGGCGGGAG A G MDM2 Ensembl:ENSG00000135679 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968997044 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12018321 RMVar_hsa_circ_3503,RMVar_hsa_circ_118742,RMVar_hsa_circ_38758,RMVar_hsa_circ_158126,RMVar_hsa_circ_28606,RMVar_hsa_circ_360939,RMVar_hsa_circ_36682,RMVar_hsa_circ_268768,RMVar_hsa_circ_285716,RMVar_hsa_circ_158135,RMVar_hsa_circ_158136 32354 RMVar_ID_32354 Human_SNP_ID_505456809 A-to-I Human chr12 + 68832544 68832544 68832544 ATATATTTTTTAAATTTTTGAGACAGTCTCTCACTCCGTTGCCCAGGCGGGAGTGCAGCGCATGA ATATATTTTTTAAATTTTTGAGACAGTCTCTCGCTCCGTTGCCCAGGCGGGAGTGCAGCGCATGA A G MDM2 Ensembl:ENSG00000135679 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978969669 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3503,RMVar_hsa_circ_118742,RMVar_hsa_circ_38758,RMVar_hsa_circ_158126,RMVar_hsa_circ_28606,RMVar_hsa_circ_360939,RMVar_hsa_circ_36682,RMVar_hsa_circ_268768,RMVar_hsa_circ_285716,RMVar_hsa_circ_158135,RMVar_hsa_circ_158136 32355 RMVar_ID_32355 Human_SNP_ID_505456841 A-to-I Human chr12 + 68832652 68832652 68832652 TTCCTCCTCAGCCTTGAGAGTTAGCTGGGACTACAGGTGTGCACCACCACACCTGGCTAATTTTT TTCCTCCTCAGCCTTGAGAGTTAGCTGGGACTGCAGGTGTGCACCACCACACCTGGCTAATTTTT A G MDM2 Ensembl:ENSG00000135679 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1171926036 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3503,RMVar_hsa_circ_118742,RMVar_hsa_circ_38758,RMVar_hsa_circ_158126,RMVar_hsa_circ_28606,RMVar_hsa_circ_360939,RMVar_hsa_circ_36682,RMVar_hsa_circ_268768,RMVar_hsa_circ_285716,RMVar_hsa_circ_158135,RMVar_hsa_circ_158136 32356 RMVar_ID_32356 Human_SNP_ID_505457532 A-to-I Human chr12 + 68834290 68834290 68834290 ATGACGAAACCCCGTCTCCACTAAAAACATAAAAATTAGCCGGGTGTGGTAGTGGACACCTGTAA ATGACGAAACCCCGTCTCCACTAAAAACATAAGAATTAGCCGGGTGTGGTAGTGGACACCTGTAA A G MDM2 Ensembl:ENSG00000135679 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs746561074 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3503,RMVar_hsa_circ_118742,RMVar_hsa_circ_38758,RMVar_hsa_circ_158126,RMVar_hsa_circ_28606,RMVar_hsa_circ_360939,RMVar_hsa_circ_36682,RMVar_hsa_circ_268768,RMVar_hsa_circ_285716,RMVar_hsa_circ_158135,RMVar_hsa_circ_158136 32357 RMVar_ID_32357 Human_SNP_ID_505459822 A-to-I Human chr12 + 68843223 68843223 68843223 AGAGTTAAATTTGAAGGAATAAGTTCTAGCTGAAGTATTATGAACTCCAAATAATGCTTTGAGGA AGAGTTAAATTTGAAGGAATAAGTTCTAGCTGGAGTATTATGAACTCCAAATAATGCTTTGAGGA A G MDM2 Ensembl:ENSG00000135679 Protein coding 3'UTR GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-Seq:(High) rs1351454816 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6250994,Human_RBP_ID_17355887,Human_RBP_ID_17473347,Human_RBP_ID_17561205,Human_RBP_ID_18263537,Human_RBP_ID_26419385 Human_Splice_Rec_1396369 Human_miRNA_ID_1085350 RMVar_hsa_circ_268768,RMVar_hsa_circ_267506 32358 RMVar_ID_32358 Human_SNP_ID_505459824 A-to-I Human chr12 + 68843227 68843227 68843227 TTAAATTTGAAGGAATAAGTTCTAGCTGAAGTATTATGAACTCCAAATAATGCTTTGAGGACCTC TTAAATTTGAAGGAATAAGTTCTAGCTGAAGTGTTATGAACTCCAAATAATGCTTTGAGGACCTC A G MDM2 Ensembl:ENSG00000135679 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs3207628 Functional Loss SNV dbSNP153 33..33 33 - - - 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 32359 RMVar_ID_32359 Human_SNP_ID_505459825 A-to-I Human chr12 + 68843230 68843230 68843230 AATTTGAAGGAATAAGTTCTAGCTGAAGTATTATGAACTCCAAATAATGCTTTGAGGACCTCCAA AATTTGAAGGAATAAGTTCTAGCTGAAGTATTGTGAACTCCAAATAATGCTTTGAGGACCTCCAA A G MDM2 Ensembl:ENSG00000135679 Protein coding 3'UTR GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-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 32360 RMVar_ID_32360 Human_SNP_ID_505459827 A-to-I Human chr12 + 68843233 68843233 68843233 TTGAAGGAATAAGTTCTAGCTGAAGTATTATGAACTCCAAATAATGCTTTGAGGACCTCCAAAGG TTGAAGGAATAAGTTCTAGCTGAAGTATTATGGACTCCAAATAATGCTTTGAGGACCTCCAAAGG A G MDM2 Ensembl:ENSG00000135679 Protein coding 3'UTR GSE47997;GSE100210;GSE107867 K562 cells&HepG2 cells;HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 23474544,29129909,30559470 RNA-Seq:(High) rs1293612398 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6250994,Human_RBP_ID_17355887,Human_RBP_ID_17473347,Human_RBP_ID_17561205,Human_RBP_ID_26419385 Human_Splice_Rec_1396369 RMVar_hsa_circ_268768,RMVar_hsa_circ_267506 32361 RMVar_ID_32361 Human_SNP_ID_505459830 A-to-I Human chr12 + 68843239 68843239 68843239 GAATAAGTTCTAGCTGAAGTATTATGAACTCCAAATAATGCTTTGAGGACCTCCAAAGGTAAAAG GAATAAGTTCTAGCTGAAGTATTATGAACTCCCAATAATGCTTTGAGGACCTCCAAAGGTAAAAG A C MDM2 Ensembl:ENSG00000135679 Protein coding 3'UTR GSE47997;GSE100210;GSE100210 K562 cells&HepG2 cells;HepG2 cell line;HepG2 cell line - 23474544,29129909,29129909 RNA-Seq:(High) rs1317511504 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6214277,Human_RBP_ID_17355887,Human_RBP_ID_17473347,Human_RBP_ID_17561205,Human_RBP_ID_26419385 Human_Splice_Rec_1396369 RMVar_hsa_circ_268768,RMVar_hsa_circ_267506 32362 RMVar_ID_32362 Human_SNP_ID_505459831 A-to-I Human chr12 + 68843240 68843240 68843240 AATAAGTTCTAGCTGAAGTATTATGAACTCCAAATAATGCTTTGAGGACCTCCAAAGGTAAAAGT AATAAGTTCTAGCTGAAGTATTATGAACTCCAGATAATGCTTTGAGGACCTCCAAAGGTAAAAGT A G MDM2 Ensembl:ENSG00000135679 Protein coding 3'UTR GSE47997;GSE100210;GSE107867 K562 cells&HepG2 cells;HepG2 cell line;ASD brains,frontal_cortex - 23474544,29129909,30559470 RNA-Seq:(High) rs1443345961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6214277,Human_RBP_ID_17561205,Human_RBP_ID_23159129,Human_RBP_ID_26419385 Human_Splice_Rec_1396369 RMVar_hsa_circ_268768,RMVar_hsa_circ_267506 32363 RMVar_ID_32363 Human_SNP_ID_505459832 A-to-I Human chr12 + 68843243 68843242 68843243 AAGTTCTAGCTGAAGTATTATGAACTCCAAATAATGCTTTGAGGACCTCCAAAGGTAAAAGTACT AAGTTCTAGCTGAAGTATTATGAACTCCAAAT_ATGCTTTGAGGACCTCCAAAGGTAAAAGTACT TA T MDM2 Ensembl:ENSG00000135679 Protein coding 3'UTR GSE47997;GSE100210;GSE100210;GSE107867 K562 cells&HepG2 cells;HepG2 cell line;HepG2 cell line;ASD brains,cerebellum - 23474544,29129909,29129909,30559470 RNA-Seq:(High) rs533905903 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_6214277,Human_RBP_ID_12018802,Human_RBP_ID_17561205,Human_RBP_ID_23159129,Human_RBP_ID_26421516 Human_Splice_Rec_1396369 RMVar_hsa_circ_268768,RMVar_hsa_circ_267506 32364 RMVar_ID_32364 Human_SNP_ID_505459837 A-to-I Human chr12 + 68843261 68843261 68843261 TATGAACTCCAAATAATGCTTTGAGGACCTCCAAAGGTAAAAGTACTAATCCCTTTGGCCATTTA TATGAACTCCAAATAATGCTTTGAGGACCTCCGAAGGTAAAAGTACTAATCCCTTTGGCCATTTA A G MDM2 Ensembl:ENSG00000135679 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs751458930 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12018802,Human_RBP_ID_17561205,Human_RBP_ID_26421516 Human_Splice_Rec_1396369 RMVar_hsa_circ_268768,RMVar_hsa_circ_267506 32365 RMVar_ID_32365 Human_SNP_ID_505459838 A-to-I Human chr12 + 68843262 68843262 68843262 ATGAACTCCAAATAATGCTTTGAGGACCTCCAAAGGTAAAAGTACTAATCCCTTTGGCCATTTAT ATGAACTCCAAATAATGCTTTGAGGACCTCCACAGGTAAAAGTACTAATCCCTTTGGCCATTTAT A C MDM2 Ensembl:ENSG00000135679 Protein coding 3'UTR GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 29129909,30559470 RNA-Seq:(High) rs1394560637 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12018802,Human_RBP_ID_17561205,Human_RBP_ID_26421516 Human_Splice_Rec_1396369 RMVar_hsa_circ_268768,RMVar_hsa_circ_267506 32366 RMVar_ID_32366 Human_SNP_ID_505459839 A-to-I Human chr12 + 68843262 68843262 68843262 ATGAACTCCAAATAATGCTTTGAGGACCTCCAAAGGTAAAAGTACTAATCCCTTTGGCCATTTAT ATGAACTCCAAATAATGCTTTGAGGACCTCCAGAGGTAAAAGTACTAATCCCTTTGGCCATTTAT A G MDM2 Ensembl:ENSG00000135679 Protein coding 3'UTR GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 29129909,30559470 RNA-Seq:(High) rs1394560637 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12018802,Human_RBP_ID_17561205,Human_RBP_ID_26421516 Human_Splice_Rec_1396369 RMVar_hsa_circ_268768,RMVar_hsa_circ_267506 32367 RMVar_ID_32367 Human_SNP_ID_505459842 A-to-I Human chr12 + 68843267 68843266 68843267 CTCCAAATAATGCTTTGAGGACCTCCAAAGGTAAAAGTACTAATCCCTTTGGCCATTTATTGAGA CTCCAAATAATGCTTTGAGGACCTCCAAAGGT_AAAGTACTAATCCCTTTGGCCATTTATTGAGA TA T MDM2 Ensembl:ENSG00000135679 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1175756958 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_17561205,Human_RBP_ID_26421516 RMVar_hsa_circ_268768,RMVar_hsa_circ_267506 32368 RMVar_ID_32368 Human_SNP_ID_505459844 A-to-I Human chr12 + 68843267 68843267 68843267 CTCCAAATAATGCTTTGAGGACCTCCAAAGGTAAAAGTACTAATCCCTTTGGCCATTTATTGAGA CTCCAAATAATGCTTTGAGGACCTCCAAAGGTCAAAGTACTAATCCCTTTGGCCATTTATTGAGA A C MDM2 Ensembl:ENSG00000135679 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs562153503 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17561205,Human_RBP_ID_26421516 RMVar_hsa_circ_268768,RMVar_hsa_circ_267506 32369 RMVar_ID_32369 Human_SNP_ID_505459845 A-to-I Human chr12 + 68843269 68843269 68843269 CCAAATAATGCTTTGAGGACCTCCAAAGGTAAAAGTACTAATCCCTTTGGCCATTTATTGAGAGA CCAAATAATGCTTTGAGGACCTCCAAAGGTAAGAGTACTAATCCCTTTGGCCATTTATTGAGAGA A G MDM2 Ensembl:ENSG00000135679 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs529265366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17561205,Human_RBP_ID_26421516 RMVar_hsa_circ_268768,RMVar_hsa_circ_267506 32370 RMVar_ID_32370 Human_SNP_ID_505459848 A-to-I Human chr12 + 68843273 68843273 68843273 ATAATGCTTTGAGGACCTCCAAAGGTAAAAGTACTAATCCCTTTGGCCATTTATTGAGAGAGAGA ATAATGCTTTGAGGACCTCCAAAGGTAAAAGTGCTAATCCCTTTGGCCATTTATTGAGAGAGAGA A G MDM2 Ensembl:ENSG00000135679 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1211910103 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_426750,Human_RBP_ID_4259327,Human_RBP_ID_17561205,Human_RBP_ID_26421516,Human_RBP_ID_27424816 RMVar_hsa_circ_268768,RMVar_hsa_circ_267506 32371 RMVar_ID_32371 Human_SNP_ID_505459957 A-to-I Human chr12 + 68843729 68843729 68843729 AACTCTCTCTCTCTCTCTCTGTCTGTCTCAATAAATGGCCAAAGGGATTAGTAGTTTACCTGTGG AACTCTCTCTCTCTCTCTCTGTCTGTCTCAATGAATGGCCAAAGGGATTAGTAGTTTACCTGTGG A G MDM2 Ensembl:ENSG00000135679 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;HepG2 cell line - 23474544,24183664,29129909,29129909 RNA-Seq:(High) rs1315346525 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6214290,Human_RBP_ID_12018815,Human_RBP_ID_17825691,Human_RBP_ID_18263546,Human_RBP_ID_23159136,Human_RBP_ID_26421518,Human_RBP_ID_27632576 Human_miRNA_ID_877610,Human_miRNA_ID_1809442 RMVar_hsa_circ_268768,RMVar_hsa_circ_267506 32372 RMVar_ID_32372 Human_SNP_ID_505459958 A-to-I Human chr12 + 68843737 68843737 68843737 CTCTCTCTCTCTGTCTGTCTCAATAAATGGCCAAAGGGATTAGTAGTTTACCTGTGGAGGTCCTC CTCTCTCTCTCTGTCTGTCTCAATAAATGGCCCAAGGGATTAGTAGTTTACCTGTGGAGGTCCTC A C MDM2 Ensembl:ENSG00000135679 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1022464252 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6214290,Human_RBP_ID_12018815,Human_RBP_ID_17685228,Human_RBP_ID_17825691,Human_RBP_ID_18263546,Human_RBP_ID_23159136,Human_RBP_ID_26421518,Human_RBP_ID_27632576 Human_Splice_Rec_1396371 Human_miRNA_ID_877610,Human_miRNA_ID_1809442 RMVar_hsa_circ_268768,RMVar_hsa_circ_267506 32373 RMVar_ID_32373 Human_SNP_ID_505459959 A-to-I Human chr12 + 68843737 68843737 68843737 CTCTCTCTCTCTGTCTGTCTCAATAAATGGCCAAAGGGATTAGTAGTTTACCTGTGGAGGTCCTC CTCTCTCTCTCTGTCTGTCTCAATAAATGGCCGAAGGGATTAGTAGTTTACCTGTGGAGGTCCTC A G MDM2 Ensembl:ENSG00000135679 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1022464252 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6214290,Human_RBP_ID_12018815,Human_RBP_ID_17685228,Human_RBP_ID_17825691,Human_RBP_ID_18263546,Human_RBP_ID_23159136,Human_RBP_ID_26421518,Human_RBP_ID_27632576 Human_Splice_Rec_1396371 Human_miRNA_ID_877610,Human_miRNA_ID_1809442 RMVar_hsa_circ_268768,RMVar_hsa_circ_267506 32374 RMVar_ID_32374 Human_SNP_ID_505459960 A-to-I Human chr12 + 68843738 68843738 68843738 TCTCTCTCTCTGTCTGTCTCAATAAATGGCCAAAGGGATTAGTAGTTTACCTGTGGAGGTCCTCC TCTCTCTCTCTGTCTGTCTCAATAAATGGCCATAGGGATTAGTAGTTTACCTGTGGAGGTCCTCC A T MDM2 Ensembl:ENSG00000135679 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs543869982 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6214290,Human_RBP_ID_12018815,Human_RBP_ID_17685228,Human_RBP_ID_17825691,Human_RBP_ID_18263546,Human_RBP_ID_23159136,Human_RBP_ID_26421518,Human_RBP_ID_27632576 Human_Splice_Rec_1396371 Human_miRNA_ID_877610,Human_miRNA_ID_1809442 RMVar_hsa_circ_268768,RMVar_hsa_circ_267506 32375 RMVar_ID_32375 Human_SNP_ID_505459963 A-to-I Human chr12 + 68843746 68843746 68843746 TCTGTCTGTCTCAATAAATGGCCAAAGGGATTAGTAGTTTACCTGTGGAGGTCCTCCAAGCATTA TCTGTCTGTCTCAATAAATGGCCAAAGGGATTGGTAGTTTACCTGTGGAGGTCCTCCAAGCATTA A G MDM2 Ensembl:ENSG00000135679 Protein coding 3'UTR GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs1325440222 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 32376 RMVar_ID_32376 Human_SNP_ID_505459964 A-to-I Human chr12 + 68843749 68843749 68843749 GTCTGTCTCAATAAATGGCCAAAGGGATTAGTAGTTTACCTGTGGAGGTCCTCCAAGCATTATTT GTCTGTCTCAATAAATGGCCAAAGGGATTAGTGGTTTACCTGTGGAGGTCCTCCAAGCATTATTT A G MDM2 Ensembl:ENSG00000135679 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-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 32377 RMVar_ID_32377 Human_SNP_ID_505459966 A-to-I Human chr12 + 68843754 68843754 68843754 TCTCAATAAATGGCCAAAGGGATTAGTAGTTTACCTGTGGAGGTCCTCCAAGCATTATTTGGAGT TCTCAATAAATGGCCAAAGGGATTAGTAGTTTGCCTGTGGAGGTCCTCCAAGCATTATTTGGAGT A G MDM2 Ensembl:ENSG00000135679 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs11556780 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_426754,Human_RBP_ID_4239429,Human_RBP_ID_6214290,Human_RBP_ID_12018817,Human_RBP_ID_17561206,Human_RBP_ID_17685228,Human_RBP_ID_17825692,Human_RBP_ID_18263546,Human_RBP_ID_26421518,Human_RBP_ID_27424817 Human_Splice_Rec_1396370,Human_Splice_Rec_1396371 RMVar_hsa_circ_268768,RMVar_hsa_circ_267506 32378 RMVar_ID_32378 Human_SNP_ID_505459970 A-to-I Human chr12 + 68843778 68843778 68843778 AGTAGTTTACCTGTGGAGGTCCTCCAAGCATTATTTGGAGTTGATAATACTTCAGCTACAACCAA AGTAGTTTACCTGTGGAGGTCCTCCAAGCATTGTTTGGAGTTGATAATACTTCAGCTACAACCAA A G MDM2 Ensembl:ENSG00000135679 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1130177 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_426754,Human_RBP_ID_17561206,Human_RBP_ID_17825692,Human_RBP_ID_26421518,Human_RBP_ID_27424817 Human_Splice_Rec_1396368,Human_Splice_Rec_1396370,Human_Splice_Rec_1396371 Human_miRNA_ID_359172 RMVar_hsa_circ_268768,RMVar_hsa_circ_267506 32379 RMVar_ID_32379 Human_SNP_ID_505460008 A-to-I Human chr12 + 68843941 68843941 68843941 TAGAATCTGTTTTTTTCCTTTGGAGGTCCTCAAAGCATTATTGGAGTTCATAATACTGAAGCTAG TAGAATCTGTTTTTTTCCTTTGGAGGTCCTCAGAGCATTATTGGAGTTCATAATACTGAAGCTAG A G MDM2 Ensembl:ENSG00000135679 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs563860571 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6214304,Human_RBP_ID_12018828,Human_RBP_ID_17473351,Human_RBP_ID_26419394 Human_Splice_Rec_1396372 RMVar_hsa_circ_268768,RMVar_hsa_circ_267506 32380 RMVar_ID_32380 Human_SNP_ID_505460016 A-to-I Human chr12 + 68843960 68843960 68843960 TTGGAGGTCCTCAAAGCATTATTGGAGTTCATAATACTGAAGCTAGAACCAAGCAGAATCTGTTT TTGGAGGTCCTCAAAGCATTATTGGAGTTCATGATACTGAAGCTAGAACCAAGCAGAATCTGTTT A G MDM2 Ensembl:ENSG00000135679 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs10761 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1476569,Human_RBP_ID_4239438,Human_RBP_ID_6214304,Human_RBP_ID_8785008,Human_RBP_ID_12018829,Human_RBP_ID_17825697,Human_RBP_ID_18263552,Human_RBP_ID_18632451,Human_RBP_ID_26419394,Human_RBP_ID_27632579 Human_Splice_Rec_1396372 RMVar_hsa_circ_268768,RMVar_hsa_circ_267506 32381 RMVar_ID_32381 Human_SNP_ID_505461155 A-to-I Human chr12 + 68847901 68847901 68847901 AAAATAACATCCTGGGCCAGGCTCTGTGACTCACGCCTGTAATCTCAACACTTTGGGAGGCCAAG AAAATAACATCCTGGGCCAGGCTCTGTGACTCGCGCCTGTAATCTCAACACTTTGGGAGGCCAAG A G MDM2 Ensembl:ENSG00000135679 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1291827012 Functional Loss SNV dbSNP153 33..33 33 - - - 32382 RMVar_ID_32382 Human_SNP_ID_505461156 A-to-I Human chr12 + 68847901 68847901 68847901 AAAATAACATCCTGGGCCAGGCTCTGTGACTCACGCCTGTAATCTCAACACTTTGGGAGGCCAAG AAAATAACATCCTGGGCCAGGCTCTGTGACTCTCGCCTGTAATCTCAACACTTTGGGAGGCCAAG A T MDM2 Ensembl:ENSG00000135679 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1291827012 Functional Loss SNV dbSNP153 33..33 33 - - - 32383 RMVar_ID_32383 Human_SNP_ID_505461600 A-to-I Human chr12 + 68849474 68849474 68849474 TCTCTCACTCCAGGTTGGAGTGCAGTGGCACTATCTCAGCTCACTGCAAACTCTGCCTCCCAAGG TCTCTCACTCCAGGTTGGAGTGCAGTGGCACTGTCTCAGCTCACTGCAAACTCTGCCTCCCAAGG A G MDM2 Ensembl:ENSG00000135679 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1401661371 Functional Loss SNV dbSNP153 33..33 33 - - - 32384 RMVar_ID_32384 Human_SNP_ID_505461612 A-to-I Human chr12 + 68849510 68849510 68849510 CAGCTCACTGCAAACTCTGCCTCCCAAGGTCAAATGATTCTCCTGCCTCAGCCTCCCAGTAGTTG CAGCTCACTGCAAACTCTGCCTCCCAAGGTCAGATGATTCTCCTGCCTCAGCCTCCCAGTAGTTG A G MDM2 Ensembl:ENSG00000135679 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1476130128 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12018968 32385 RMVar_ID_32385 Human_SNP_ID_505461627 A-to-I Human chr12 + 68849584 68849584 68849584 GCGCATGCCACCATGCATGGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGCTAG GCGCATGCCACCATGCATGGCTAATTTTTTGTGTTTTTAGTAGAGACGGGGTTTCACCATGCTAG A G MDM2 Ensembl:ENSG00000135679 Protein coding 3'UTR GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs550986331 Functional Loss SNV dbSNP153 33..33 33 - - - 32386 RMVar_ID_32386 Human_SNP_ID_505461683 A-to-I Human chr12 + 68849827 68849827 68849827 TAGAGATGGGGTTTTGCTATGTTAGCCAGGCTAGTCTCGAACTCCTGACCTCAGGTGATCCAGTC TAGAGATGGGGTTTTGCTATGTTAGCCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCCAGTC A G MDM2 Ensembl:ENSG00000135679 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs940378508 Functional Loss SNV dbSNP153 33..33 33 - - - 32387 RMVar_ID_32387 Human_SNP_ID_505461762 A-to-I Human chr12 + 68850171 68850171 68850171 GCCAGGCGTCATGGCATGTGCCTGTTAATTCCAGCTGCTCGAGAGGCTGAGGCATGAGAATTACT GCCAGGCGTCATGGCATGTGCCTGTTAATTCCGGCTGCTCGAGAGGCTGAGGCATGAGAATTACT A G MDM2 Ensembl:ENSG00000135679 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1462143801 Functional Loss SNV dbSNP153 33..33 33 - - - 32388 RMVar_ID_32388 Human_SNP_ID_505461780 A-to-I Human chr12 + 68850268 68850268 68850268 AGATCCCACCACTGCACTCCAGCCTGGGTGACAGAGCGAGACTTCGTCCCAAAAAAAAAAAAAAA AGATCCCACCACTGCACTCCAGCCTGGGTGACGGAGCGAGACTTCGTCCCAAAAAAAAAAAAAAA A G MDM2 Ensembl:ENSG00000135679 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559961699 Functional Loss SNV dbSNP153 33..33 33 - - - 32389 RMVar_ID_32389 Human_SNP_ID_505462080 A-to-I Human chr12 - 68851525 68851525 68851525 CTCACTGCAACCTCTGCCTCCCGGGTTCAAGCAATTCTCCTGTCTCAGCCTCCCGAGTACCTGGG CTCACTGCAACCTCTGCCTCCCGGGTTCAAGCGATTCTCCTGTCTCAGCCTCCCGAGTACCTGGG T C CPM Ensembl:ENSG00000135678 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1320540250 Functional Loss SNV dbSNP153 33..33 33 - - - 32390 RMVar_ID_32390 Human_SNP_ID_505462081 A-to-I Human chr12 - 68851528 68851528 68851528 CGGCTCACTGCAACCTCTGCCTCCCGGGTTCAAGCAATTCTCCTGTCTCAGCCTCCCGAGTACCT CGGCTCACTGCAACCTCTGCCTCCCGGGTTCAGGCAATTCTCCTGTCTCAGCCTCCCGAGTACCT T C CPM Ensembl:ENSG00000135678 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1435875853 Functional Loss SNV dbSNP153 33..33 33 - - - 32391 RMVar_ID_32391 Human_SNP_ID_505462428 A-to-I Human chr12 - 68852649 68852649 68852649 GGAGGCTGAGGCAGGAGAAATCGCCTGAACCCAGAAGGCAGAGGTTGCAGTGAGCCAAGATCACA GGAGGCTGAGGCAGGAGAAATCGCCTGAACCCTGAAGGCAGAGGTTGCAGTGAGCCAAGATCACA T A CPM Ensembl:ENSG00000135678 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1206922619 Functional Loss SNV dbSNP153 33..33 33 - - - 32392 RMVar_ID_32392 Human_SNP_ID_505462437 A-to-I Human chr12 - 68852690 68852690 68852690 AGCCGGGCGTGGTGGCAGGCACCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAAATCGC AGCCGGGCGTGGTGGCAGGCACCTGTAATCCCTGCTACTTGGGAGGCTGAGGCAGGAGAAATCGC T A CPM Ensembl:ENSG00000135678 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs964622385 Functional Loss SNV dbSNP153 33..33 33 - - - 32393 RMVar_ID_32393 Human_SNP_ID_505559992 A-to-I Human chr12 + 69245828 69245828 69245828 GAAGTGTAGGCCAGGTGCGGTGGCTCATGCCTATAATTCCAGCAGTTTGGGAGGCTGAAGTAGGC GAAGTGTAGGCCAGGTGCGGTGGCTCATGCCTGTAATTCCAGCAGTTTGGGAGGCTGAAGTAGGC A G CPSF6 Ensembl:ENSG00000111605 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1171044591 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24998643 32394 RMVar_ID_32394 Human_SNP_ID_505560029 A-to-I Human chr12 + 69246007 69246007 69246007 TACTTCAGAGGCTGAGGCAGGAGAATTGCTTGAACCTGGGGGGCAGAGGCTGCAGTGAGCTGAGA TACTTCAGAGGCTGAGGCAGGAGAATTGCTTGTACCTGGGGGGCAGAGGCTGCAGTGAGCTGAGA A T CPSF6 Ensembl:ENSG00000111605 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350031464 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12019617 32395 RMVar_ID_32395 Human_SNP_ID_505562861 A-to-I Human chr12 + 69256139 69256139 69256139 AAGAAGGCTGGTCACAAGGGACCTCCTATTGTATGATTCCATTTAGATGAAATGTCTAGGATAGG AAGAAGGCTGGTCACAAGGGACCTCCTATTGTGTGATTCCATTTAGATGAAATGTCTAGGATAGG A G CPSF6 Ensembl:ENSG00000111605 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs745498852 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_158146,RMVar_hsa_circ_88880,RMVar_hsa_circ_277579,RMVar_hsa_circ_286191,RMVar_hsa_circ_105735,RMVar_hsa_circ_158148,RMVar_hsa_circ_158147,RMVar_hsa_circ_158144,RMVar_hsa_circ_158145,RMVar_hsa_circ_158143,RMVar_hsa_circ_158149,RMVar_hsa_circ_334555,RMVar_hsa_circ_353172,RMVar_hsa_circ_113212 32396 RMVar_ID_32396 Human_SNP_ID_505594454 A-to-I Human chr12 + 69387424 69387424 69387424 TTCTTCCAGAATTACAAGTACATATATATTCTATAACAGTTCCATTTCCAGGAATTTATCCTACA TTCTTCCAGAATTACAAGTACATATATATTCTGTAACAGTTCCATTTCCAGGAATTTATCCTACA A G YEATS4 Ensembl:ENSG00000127337 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs315116 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22572961 RMVar_hsa_circ_158168,RMVar_hsa_circ_102659,RMVar_hsa_circ_124101,RMVar_hsa_circ_158166,RMVar_hsa_circ_81916,RMVar_hsa_circ_158170 32397 RMVar_ID_32397 Human_SNP_ID_505594455 A-to-I Human chr12 + 69387424 69387424 69387424 TTCTTCCAGAATTACAAGTACATATATATTCTATAACAGTTCCATTTCCAGGAATTTATCCTACA TTCTTCCAGAATTACAAGTACATATATATTCTTTAACAGTTCCATTTCCAGGAATTTATCCTACA A T YEATS4 Ensembl:ENSG00000127337 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs315116 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22572961 RMVar_hsa_circ_158168,RMVar_hsa_circ_102659,RMVar_hsa_circ_124101,RMVar_hsa_circ_158166,RMVar_hsa_circ_81916,RMVar_hsa_circ_158170 32398 RMVar_ID_32398 Human_SNP_ID_505599887 A-to-I Human chr12 + 69411229 69411229 69411229 ACATTTCACTGCAGCCTTGACCTCTCTGGCTCAGGTGATCCTCCCACCTCAGCCTCCCGAGTAGC ACATTTCACTGCAGCCTTGACCTCTCTGGCTCCGGTGATCCTCCCACCTCAGCCTCCCGAGTAGC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1161388447 Functional Loss SNV dbSNP153 33..33 33 - - - 32399 RMVar_ID_32399 Human_SNP_ID_505599888 A-to-I Human chr12 + 69411229 69411229 69411229 ACATTTCACTGCAGCCTTGACCTCTCTGGCTCAGGTGATCCTCCCACCTCAGCCTCCCGAGTAGC ACATTTCACTGCAGCCTTGACCTCTCTGGCTCGGGTGATCCTCCCACCTCAGCCTCCCGAGTAGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1161388447 Functional Loss SNV dbSNP153 33..33 33 - - - 32400 RMVar_ID_32400 Human_SNP_ID_505600500 A-to-I Human chr12 + 69413758 69413758 69413758 CCTATGGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATTGTTTGAACCCAGGAAGCAGAGGTT CCTATGGTCCCAGCTACTTGGGAGGCTGAGGCGGGAGAATTGTTTGAACCCAGGAAGCAGAGGTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs936865821 Functional Loss SNV dbSNP153 33..33 33 - - - 32401 RMVar_ID_32401 Human_SNP_ID_505603446 A-to-I Human chr12 + 69426600 69426600 69426600 ATCATATTAGTCACGCTGATCTCGAACTCCTGACCTCAGGTGATCCGCCTGCCTCAGCCTCCCAA ATCATATTAGTCACGCTGATCTCGAACTCCTGGCCTCAGGTGATCCGCCTGCCTCAGCCTCCCAA A G lnc-YEATS4-4 RNACentral:URS00008BBE3A lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1446659512 Functional Loss SNV dbSNP153 33..33 33 - - - 32402 RMVar_ID_32402 Human_SNP_ID_505619252 A-to-I Human chr12 + 69491695 69491695 69491695 CATTTCCAGCTAAGTTTTTAAAATTTTGTTGTAGAGACGGGGACTCACTATGTTGTCCATGCTGG CATTTCCAGCTAAGTTTTTAAAATTTTGTTGTGGAGACGGGGACTCACTATGTTGTCCATGCTGG A G FRS2 Ensembl:ENSG00000166225 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1351709908 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12022330 RMVar_hsa_circ_90896,RMVar_hsa_circ_158174,RMVar_hsa_circ_158175,RMVar_hsa_circ_358712 32403 RMVar_ID_32403 Human_SNP_ID_505632914 A-to-I Human chr12 + 69546463 69546463 69546463 TATTTTTATTAGAGGCAGGGTTTTGCTATGTTACCTGGGCTGGTCTTGAACTCCTGGCCTCAAGT TATTTTTATTAGAGGCAGGGTTTTGCTATGTTCCCTGGGCTGGTCTTGAACTCCTGGCCTCAAGT A C FRS2 Ensembl:ENSG00000166225 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs762212909 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13315,RMVar_hsa_circ_90896,RMVar_hsa_circ_158174,RMVar_hsa_circ_15640,RMVar_hsa_circ_158175,RMVar_hsa_circ_276864,RMVar_hsa_circ_158177,RMVar_hsa_circ_158178,RMVar_hsa_circ_158176,RMVar_hsa_circ_52950,RMVar_hsa_circ_65799,RMVar_hsa_circ_158179,RMVar_hsa_circ_44410 32404 RMVar_ID_32404 Human_SNP_ID_505634505 A-to-I Human chr12 + 69553135 69553135 69553135 ACTCTGTTGCCCAGGCTGGAGTGCAGTGGCACAATCTCGGCTCACTGCAACCTCCGCCTCCCAGG ACTCTGTTGCCCAGGCTGGAGTGCAGTGGCACGATCTCGGCTCACTGCAACCTCCGCCTCCCAGG A G FRS2 Ensembl:ENSG00000166225 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1279110847 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13315,RMVar_hsa_circ_90896,RMVar_hsa_circ_158174,RMVar_hsa_circ_15640,RMVar_hsa_circ_158175,RMVar_hsa_circ_276864,RMVar_hsa_circ_158177,RMVar_hsa_circ_158178,RMVar_hsa_circ_158176,RMVar_hsa_circ_52950,RMVar_hsa_circ_65799,RMVar_hsa_circ_158179,RMVar_hsa_circ_44410 32405 RMVar_ID_32405 Human_SNP_ID_505645023 A-to-I Human chr12 + 69593043 69593043 69593043 AAAGGTTGCAGAAATAGAACATGCGGAAAAGGAAAAAATGAAGGAGAAAGTTGAACGTATTCTTA AAAGGTTGCAGAAATAGAACATGCGGAAAAGGGAAAAATGAAGGAGAAAGTTGAACGTATTCTTA A G CCT2 Ensembl:ENSG00000166226 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1168613483 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_35204,Human_RBP_ID_1477090,Human_RBP_ID_1800708,Human_RBP_ID_6216194,Human_RBP_ID_23572881 Human_Splice_Rec_1396834,Human_Splice_Rec_1396835,Human_Splice_Rec_1396870,Human_Splice_Rec_1396871,Human_Splice_Rec_1396898,Human_Splice_Rec_1396899,Human_Splice_Rec_1396926,Human_Splice_Rec_1396927,Human_Splice_Rec_1396944,Human_Splice_Rec_1396945,Human_Splice_Rec_1396949 Human_miRNA_ID_547347,Human_miRNA_ID_2195613 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_271140,RMVar_hsa_circ_349898,RMVar_hsa_circ_104851,RMVar_hsa_circ_158193,RMVar_hsa_circ_158195,RMVar_hsa_circ_41931,RMVar_hsa_circ_158196,RMVar_hsa_circ_158194,RMVar_hsa_circ_365359,RMVar_hsa_circ_316880,RMVar_hsa_circ_158198,RMVar_hsa_circ_158197 32406 RMVar_ID_32406 Human_SNP_ID_169105130 A-to-I Human chr3 - 195067501 195067501 195067501 TGGTGGTGCACGCCCAGCTATTCAGGAGGCTGAGCTGGGAGGATCACTCAAACCCAGGAGGCAGA TGGTGGTGCACGCCCAGCTATTCAGGAGGCTGGGCTGGGAGGATCACTCAAACCCAGGAGGCAGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1356781002 Functional Loss SNV dbSNP153 33..33 33 - - - 32407 RMVar_ID_32407 Human_SNP_ID_169141783 A-to-I Human chr3 - 195205641 195205641 195205641 CCAGGCTGGTTTTGAACTCGTGACCTTGGGTAATTCACCCGCCTCGGCCTCCCACAGTGCTGGGA CCAGGCTGGTTTTGAACTCGTGACCTTGGGTAGTTCACCCGCCTCGGCCTCCCACAGTGCTGGGA T C XXYLT1 Ensembl:ENSG00000173950 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1212921563 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101781,RMVar_hsa_circ_104920,RMVar_hsa_circ_223762,RMVar_hsa_circ_223763,RMVar_hsa_circ_271065,RMVar_hsa_circ_13539,RMVar_hsa_circ_223767 32408 RMVar_ID_32408 Human_SNP_ID_169141784 A-to-I Human chr3 - 195205641 195205641 195205641 CCAGGCTGGTTTTGAACTCGTGACCTTGGGTAATTCACCCGCCTCGGCCTCCCACAGTGCTGGGA CCAGGCTGGTTTTGAACTCGTGACCTTGGGTACTTCACCCGCCTCGGCCTCCCACAGTGCTGGGA T G XXYLT1 Ensembl:ENSG00000173950 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1212921563 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101781,RMVar_hsa_circ_104920,RMVar_hsa_circ_223762,RMVar_hsa_circ_223763,RMVar_hsa_circ_271065,RMVar_hsa_circ_13539,RMVar_hsa_circ_223767 32409 RMVar_ID_32409 Human_SNP_ID_169165235 A-to-I Human chr3 - 195299352 195299351 195299353 TTGCAAAGGCTGTTCTTGAACTCCTGGCCTCAAGTGATCTGCCTGCCTCGGCCTCCCAAAGTGCT TTGCAAAGGCTGTTCTTGAACTCCTGGCCTC__GTGATCTGCCTGCCTCGGCCTCCCAAAGTGCT CTT C ACAP2 Ensembl:ENSG00000114331 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1204068768 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_1688,RMVar_hsa_circ_34490,RMVar_hsa_circ_101099,RMVar_hsa_circ_353046,RMVar_hsa_circ_375876,RMVar_hsa_circ_325798,RMVar_hsa_circ_92803,RMVar_hsa_circ_16229,RMVar_hsa_circ_223777,RMVar_hsa_circ_20719,RMVar_hsa_circ_32736,RMVar_hsa_circ_223778,RMVar_hsa_circ_223779,RMVar_hsa_circ_223780,RMVar_hsa_circ_330883,RMVar_hsa_circ_338334,RMVar_hsa_circ_354490,RMVar_hsa_circ_121827,RMVar_hsa_circ_223782,RMVar_hsa_circ_223781,RMVar_hsa_circ_74365,RMVar_hsa_circ_265772,RMVar_hsa_circ_331128,RMVar_hsa_circ_323932,RMVar_hsa_circ_21306,RMVar_hsa_circ_47865,RMVar_hsa_circ_677,RMVar_hsa_circ_223784,RMVar_hsa_circ_267644,RMVar_hsa_circ_358200,RMVar_hsa_circ_223785,RMVar_hsa_circ_321122,RMVar_hsa_circ_44207,RMVar_hsa_circ_223786,RMVar_hsa_circ_223787 32410 RMVar_ID_32410 Human_SNP_ID_169165539 A-to-I Human chr3 - 195300107 195300107 195300107 AGGAGGCAGAGGTTGCAGTGAGCCGAGATCGCACCACTGCACTCCGGCCTGGGCAACAGAGGAAG AGGAGGCAGAGGTTGCAGTGAGCCGAGATCGCGCCACTGCACTCCGGCCTGGGCAACAGAGGAAG T C ACAP2 Ensembl:ENSG00000114331 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982075947 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25724216 RMVar_hsa_circ_1688,RMVar_hsa_circ_34490,RMVar_hsa_circ_101099,RMVar_hsa_circ_353046,RMVar_hsa_circ_375876,RMVar_hsa_circ_325798,RMVar_hsa_circ_92803,RMVar_hsa_circ_16229,RMVar_hsa_circ_223777,RMVar_hsa_circ_20719,RMVar_hsa_circ_32736,RMVar_hsa_circ_223778,RMVar_hsa_circ_223779,RMVar_hsa_circ_223780,RMVar_hsa_circ_330883,RMVar_hsa_circ_338334,RMVar_hsa_circ_354490,RMVar_hsa_circ_121827,RMVar_hsa_circ_223782,RMVar_hsa_circ_223781,RMVar_hsa_circ_74365,RMVar_hsa_circ_265772,RMVar_hsa_circ_331128,RMVar_hsa_circ_323932,RMVar_hsa_circ_21306,RMVar_hsa_circ_47865,RMVar_hsa_circ_677,RMVar_hsa_circ_223784,RMVar_hsa_circ_267644,RMVar_hsa_circ_358200,RMVar_hsa_circ_223785,RMVar_hsa_circ_321122,RMVar_hsa_circ_44207,RMVar_hsa_circ_223786,RMVar_hsa_circ_223787 32411 RMVar_ID_32411 Human_SNP_ID_169193977 A-to-I Human chr3 - 195418657 195418657 195418657 GGGACGCCGTGGTGGGAGGATTGCTTGAGGCCAGGTGTTTGAGACCAGACTGGGCAACATAGCCT GGGACGCCGTGGTGGGAGGATTGCTTGAGGCCGGGTGTTTGAGACCAGACTGGGCAACATAGCCT T C ACAP2 Ensembl:ENSG00000114331 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1361355473 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104683,RMVar_hsa_circ_223789 32412 RMVar_ID_32412 Human_SNP_ID_169196650 A-to-I Human chr3 - 195428405 195428405 195428405 CGCTGTTGTATTTGTGGTCTGTTGATTGGAATATGACTGTGTGTGTATATATATGTATAGACCTA CGCTGTTGTATTTGTGGTCTGTTGATTGGAATGTGACTGTGTGTGTATATATATGTATAGACCTA T C ACAP2 Ensembl:ENSG00000114331 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs972564351 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104683,RMVar_hsa_circ_223789 32413 RMVar_ID_32413 Human_SNP_ID_169196676 A-to-I Human chr3 - 195428518 195428518 195428518 TGTTATTGTACTGAATACTGTAGGCAATTTTAACACAGTGGCATTTGTGTATCTAAACATATCTA TGTTATTGTACTGAATACTGTAGGCAATTTTACCACAGTGGCATTTGTGTATCTAAACATATCTA T G ACAP2 Ensembl:ENSG00000114331 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1243141619 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104683,RMVar_hsa_circ_223789 32414 RMVar_ID_32414 Human_SNP_ID_169196692 A-to-I Human chr3 - 195428617 195428617 195428617 ATCATAGGGTGTATTTACACAACTTAGATGGTATAGCCTACTACACATCTAGGGTATATGATATA ATCATAGGGTGTATTTACACAACTTAGATGGTGTAGCCTACTACACATCTAGGGTATATGATATA T C ACAP2 Ensembl:ENSG00000114331 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs948367772 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104683,RMVar_hsa_circ_223789 32415 RMVar_ID_32415 Human_SNP_ID_169199263 A-to-I Human chr3 - 195438683 195438683 195438683 AATTATGTTTGAGAGACAGAGTCTTACTTGTTATCCAGGCTGTTCTCCAACTCCTGGACTCAGGT AATTATGTTTGAGAGACAGAGTCTTACTTGTTGTCCAGGCTGTTCTCCAACTCCTGGACTCAGGT T C ACAP2 Ensembl:ENSG00000114331 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1055034323 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104683,RMVar_hsa_circ_223789 32416 RMVar_ID_32416 Human_SNP_ID_169250940 A-to-I Human chr3 - 195520141 195520141 195520141 GCCAGGAGTGGTAGCACATGCCTGTGATCCCAACTACTCGGGAGACTGAGGCAGGAGAATCGCTT GCCAGGAGTGGTAGCACATGCCTGTGATCCCAGCTACTCGGGAGACTGAGGCAGGAGAATCGCTT T C PPP1R2 Ensembl:ENSG00000184203 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs573295737 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57590,RMVar_hsa_circ_360821 32417 RMVar_ID_32417 Human_SNP_ID_169251016 A-to-I Human chr3 - 195520437 195520437 195520437 CAGCTAATTTTTTGTAATTTTTTTGTAGAGATAGGTTCTTGCCATGTTGCCCAGGCTGGTCTTGA CAGCTAATTTTTTGTAATTTTTTTGTAGAGATGGGTTCTTGCCATGTTGCCCAGGCTGGTCTTGA T C PPP1R2 Ensembl:ENSG00000184203 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1213434934 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57590,RMVar_hsa_circ_360821 32418 RMVar_ID_32418 Human_SNP_ID_169251023 A-to-I Human chr3 - 195520468 195520468 195520468 AGCTGGGACCACAGTCGTGTACTACCACACCCAGCTAATTTTTTGTAATTTTTTTGTAGAGATAG AGCTGGGACCACAGTCGTGTACTACCACACCCGGCTAATTTTTTGTAATTTTTTTGTAGAGATAG T C PPP1R2 Ensembl:ENSG00000184203 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs965326157 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57590,RMVar_hsa_circ_360821 32419 RMVar_ID_32419 Human_SNP_ID_169251039 A-to-I Human chr3 - 195520536 195520536 195520536 ATAGTCGCGGCTCACTGCAGTTTCAGCCTTCTAAGCTTAGCCAGTCCTCCCATCTCAGCCTTCCC ATAGTCGCGGCTCACTGCAGTTTCAGCCTTCTGAGCTTAGCCAGTCCTCCCATCTCAGCCTTCCC T C PPP1R2 Ensembl:ENSG00000184203 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1484121066 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57590,RMVar_hsa_circ_360821 32420 RMVar_ID_32420 Human_SNP_ID_169251120 A-to-I Human chr3 - 195520814 195520814 195520814 AAATCAAACAAAGAGAAAGTACTTTGGAGGCCAGGTGTGGTGGCACGCATCTGTAGTTCCAGTTA AAATCAAACAAAGAGAAAGTACTTTGGAGGCCGGGTGTGGTGGCACGCATCTGTAGTTCCAGTTA T C PPP1R2 Ensembl:ENSG00000184203 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs563471985 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57590,RMVar_hsa_circ_360821 32421 RMVar_ID_32421 Human_SNP_ID_169251187 A-to-I Human chr3 - 195521126 195521126 195521126 TATTTTCAGTAGAGACGGGGTTTCACCATGTTAGCCAGGATGTTCTCAAACTCCTGACCTCATGA TATTTTCAGTAGAGACGGGGTTTCACCATGTTGGCCAGGATGTTCTCAAACTCCTGACCTCATGA T C PPP1R2 Ensembl:ENSG00000184203 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1407679515 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57590,RMVar_hsa_circ_360821 32422 RMVar_ID_32422 Human_SNP_ID_169251191 A-to-I Human chr3 - 195521134 195521134 195521134 ATTTTTTGTATTTTCAGTAGAGACGGGGTTTCACCATGTTAGCCAGGATGTTCTCAAACTCCTGA ATTTTTTGTATTTTCAGTAGAGACGGGGTTTCGCCATGTTAGCCAGGATGTTCTCAAACTCCTGA T C PPP1R2 Ensembl:ENSG00000184203 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs564764216 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57590,RMVar_hsa_circ_360821 32423 RMVar_ID_32423 Human_SNP_ID_169251202 A-to-I Human chr3 - 195521171 195521171 195521171 AGCTGGGATTACAGACGTGTGCCACCACGCCCAGCAAATTTTTTGTATTTTCAGTAGAGACGGGG AGCTGGGATTACAGACGTGTGCCACCACGCCCGGCAAATTTTTTGTATTTTCAGTAGAGACGGGG T C PPP1R2 Ensembl:ENSG00000184203 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs550424530 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57590,RMVar_hsa_circ_360821 32424 RMVar_ID_32424 Human_SNP_ID_169251214 A-to-I Human chr3 - 195521203 195521203 195521203 TCAAGTGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGACGTGTGCCACCACGCCCA TCAAGTGATTCTCCTGCCTCAGCCTCCTGAGTGGCTGGGATTACAGACGTGTGCCACCACGCCCA T C PPP1R2 Ensembl:ENSG00000184203 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1229961901 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57590,RMVar_hsa_circ_360821 32425 RMVar_ID_32425 Human_SNP_ID_169251908 A-to-I Human chr3 - 195523972 195523972 195523972 CTAGTGCTCCCACCTCGGCCTTCCAAATAGCTAGGACCACAGGCGTGTACCACCATGCCCGGCAC CTAGTGCTCCCACCTCGGCCTTCCAAATAGCTGGGACCACAGGCGTGTACCACCATGCCCGGCAC T C PPP1R2 Ensembl:ENSG00000184203 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1337329748 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_360821,RMVar_hsa_circ_287984 32426 RMVar_ID_32426 Human_SNP_ID_169252643 A-to-I Human chr3 - 195526991 195526991 195526991 ATCACCTAAGGTCAGGAGTTCAAGACCAGCCTAGCCAACATGGTGAAACCCCGTCTCTACTGAAA ATCACCTAAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCCCGTCTCTACTGAAA T C PPP1R2 Ensembl:ENSG00000184203 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs537393133 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36909 32427 RMVar_ID_32427 Human_SNP_ID_169252813 A-to-I Human chr3 - 195527785 195527785 195527785 TATAGCACACTACAGCCTGGAACTCCCGACTCAAGTGATCCTCCCTCCTCCGCCTCCCAGGTAGC TATAGCACACTACAGCCTGGAACTCCCGACTCCAGTGATCCTCCCTCCTCCGCCTCCCAGGTAGC T G PPP1R2 Ensembl:ENSG00000184203 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1289664106 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_527611 RMVar_hsa_circ_36909 32428 RMVar_ID_32428 Human_SNP_ID_169298897 A-to-I Human chr3 + 195682817 195682817 195682817 TAATTTTTTGAGATGGAGTCTCATTGTCCCCCAGGCTGGAGTGCAGCGGCGCGATCTCAGCTCAC TAATTTTTTGAGATGGAGTCTCATTGTCCCCCCGGCTGGAGTGCAGCGGCGCGATCTCAGCTCAC A C SDHAP2,MUC20-OT1 Ensembl:ENSG00000215837,Ensembl:ENSG00000242086 Pseudogene,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1371701440 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17208973 32429 RMVar_ID_32429 Human_SNP_ID_169306273 A-to-I Human chr3 + 195700626 195700626 195700626 AAAATTAGCCAGGTGTGGTGGCACACGCCTGTAGTCCTAGCACCTTGGGAGGCTGAGGCAAGATA AAAATTAGCCAGGTGTGGTGGCACACGCCTGTGGTCCTAGCACCTTGGGAGGCTGAGGCAAGATA A G MUC20-OT1 Ensembl:ENSG00000242086 lincRNA intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs529656171 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5089867 RMVar_hsa_circ_223821,RMVar_hsa_circ_223824,RMVar_hsa_circ_223825,RMVar_hsa_circ_223826 32430 RMVar_ID_32430 Human_SNP_ID_169306487 A-to-I Human chr3 + 195701133 195701132 195701133 CCTGGCCAACGTGGTGAAAACTCGTCTCTACTAAAAATACAGCAATTAGCTGGGTGTAATAGTAG CCTGGCCAACGTGGTGAAAACTCGTCTCTACT_AAAATACAGCAATTAGCTGGGTGTAATAGTAG TA T MUC20-OT1 Ensembl:ENSG00000242086 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs149157147 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_223821,RMVar_hsa_circ_223824,RMVar_hsa_circ_223825,RMVar_hsa_circ_223826 32431 RMVar_ID_32431 Human_SNP_ID_169306996 A-to-I Human chr3 + 195702225 195702225 195702225 CTCTGTCCCCCGCCAGGCTGGAGTGCAGTGGTACGATCTCGGCTCACTGCAACCTCCACCTTCTG CTCTGTCCCCCGCCAGGCTGGAGTGCAGTGGTTCGATCTCGGCTCACTGCAACCTCCACCTTCTG A T SMBD1P,MUC20-OT1 Ensembl:ENSG00000283426,Ensembl:ENSG00000242086 Pseudogene,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1249976664 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17406636 Human_Splice_Rec_528136 RMVar_hsa_circ_223821,RMVar_hsa_circ_223825,RMVar_hsa_circ_223826 32432 RMVar_ID_32432 Human_SNP_ID_169310367 A-to-I Human chr3 - 195711066 195711066 195711066 CCAGGAGCCAGGTCCCTCCATACCTCATCTCAATTAACTCACTCACCAGGAGCCAGGTCCCTCCA CCAGGAGCCAGGTCCCTCCATACCTCATCTCAGTTAACTCACTCACCAGGAGCCAGGTCCCTCCA T C lnc-MUC4-2-001,lnc-MUC4-2-001:2,lnc-MUC4-2-002 RNACentral:URS00008C3B28,RNACentral:URS00008B2B8D,RNACentral:URS00008B8242 lincRNA,lincRNA,lincRNA exon,exon,intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1285708678 Functional Loss SNV dbSNP153 33..33 33 - - - 32433 RMVar_ID_32433 Human_SNP_ID_169311376 A-to-I Human chr3 - 195712841 195712841 195712841 GGCAGGAGGACCGGTCAGGGAGGAGTTAGGGCAGGAGGACCGGTCAGGGAGGAGTTAGGGCAGGA GGCAGGAGGACCGGTCAGGGAGGAGTTAGGGCTGGAGGACCGGTCAGGGAGGAGTTAGGGCAGGA T A lnc-MUC4-1,lnc-MUC4-1:2,lnc-MUC4-1:3,lnc-MUC4-1:4,lnc-MUC4-1:5,lnc-MUC4-1:6,lnc-MUC4-1:7,lnc-MUC4-1:8 RNACentral:URS00008B3FD5,RNACentral:URS00009AE9A5,RNACentral:URS00008B5DFF,RNACentral:URS00008B9F05,RNACentral:URS00008B3E40,RNACentral:URS00008BBB00,RNACentral:URS00008B8D8F,RNACentral:URS00008BC148 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron,intron,intron,intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs201685623 Functional Loss SNV dbSNP153 33..33 33 - - - 32434 RMVar_ID_32434 Human_SNP_ID_169311795 A-to-I Human chr3 - 195713340 195713340 195713340 GGCTGGAGGACAGGTCAGGGAGGAGTTAGGGCAGGAGGACGGGTCAGGGAGGAGTTAGGGGAGGA GGCTGGAGGACAGGTCAGGGAGGAGTTAGGGCTGGAGGACGGGTCAGGGAGGAGTTAGGGGAGGA T A lnc-MUC4-1,lnc-MUC4-1:2,lnc-MUC4-1:3,lnc-MUC4-1:4,lnc-MUC4-1:5,lnc-MUC4-1:6,lnc-MUC4-1:7,lnc-MUC4-1:8,lnc-MUC4-1:9,lnc-MUC4-1:10,lnc-MUC4-1:11 RNACentral:URS00008B3FD5,RNACentral:URS00009AE9A5,RNACentral:URS00008C0305,RNACentral:URS00008B5DFF,RNACentral:URS00008B8BE9,RNACentral:URS00008B9F05,RNACentral:URS00008B3E40,RNACentral:URS00008BBB00,RNACentral:URS00008B8D8F,RNACentral:URS00008BC148,RNACentral:URS00008BC0B7 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,intron,intron,intron,intron,exon,exon,intron,intron,exon,intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs774049789 Functional Loss SNV dbSNP153 33..33 33 - - - 32435 RMVar_ID_32435 Human_SNP_ID_169353633 A-to-I Human chr3 - 195796221 195796221 195796221 AAAATTAGCCGGGCGTGGTGGCATGCGCCTGTAATCCCAGCTACTTGGGAGGCTGAAGCAGGAGA AAAATTAGCCGGGCGTGGTGGCATGCGCCTGTGATCCCAGCTACTTGGGAGGCTGAAGCAGGAGA T C MUC4 Ensembl:ENSG00000145113 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1248462671 Functional Loss SNV dbSNP153 33..33 33 - - - 32436 RMVar_ID_32436 Human_SNP_ID_169373901 A-to-I Human chr3 - 195864051 195864051 195864051 CCGCTGCTCCTGCTGCTCCCGGGGATGGAGCAAGGCCAAGGCTGCGGGAGGCTGGGAGCCCTGCC CCGCTGCTCCTGCTGCTCCCGGGGATGGAGCAGGGCCAAGGCTGCGGGAGGCTGGGAGCCCTGCC T C TNK2 Ensembl:ENSG00000061938 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs527501023 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90669,RMVar_hsa_circ_223829 32437 RMVar_ID_32437 Human_SNP_ID_169387564 A-to-I Human chr3 - 195899425 195899425 195899425 CTACTTGGGAGGCTGAGGCAGGAGAATCGCTTAAACCCGGGAGGCAGAGGTTGCAGTCAGCCGAG CTACTTGGGAGGCTGAGGCAGGAGAATCGCTTTAACCCGGGAGGCAGAGGTTGCAGTCAGCCGAG T A TNK2 Ensembl:ENSG00000061938 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1447690195 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100106,RMVar_hsa_circ_223832 32438 RMVar_ID_32438 Human_SNP_ID_169388533 A-to-I Human chr3 - 195902878 195902878 195902878 GGGTGTGATGGTATGCTCATGTAATTCCAGCTACTTGGGAGGCCGAGGCACAAGAATCGCTTGAA GGGTGTGATGGTATGCTCATGTAATTCCAGCTGCTTGGGAGGCCGAGGCACAAGAATCGCTTGAA T C TNK2 Ensembl:ENSG00000061938 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs184395551 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100106,RMVar_hsa_circ_223832 32439 RMVar_ID_32439 Human_SNP_ID_169388876 A-to-I Human chr3 - 195904136 195904136 195904136 GTCCCACCTCAGCCTCCTGGGTAGCTGGGACTACAGGTGTGTACCACCATGCCTGGCTAATTTTT GTCCCACCTCAGCCTCCTGGGTAGCTGGGACTGCAGGTGTGTACCACCATGCCTGGCTAATTTTT T C TNK2 Ensembl:ENSG00000061938 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs953374063 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100106,RMVar_hsa_circ_223832 32440 RMVar_ID_32440 Human_SNP_ID_169391559 A-to-I Human chr3 + 195912983 195912983 195912983 CTGGGAGGCGGAGGTTGCAGGGAGCTGAGATCACGCCACTGCATTCCAGACTGGGCGACAGAGCA CTGGGAGGCGGAGGTTGCAGGGAGCTGAGATCGCGCCACTGCATTCCAGACTGGGCGACAGAGCA A G TNK2-AS1 Ensembl:ENSG00000224614 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1338016009 Functional Loss SNV dbSNP153 33..33 33 - - - 32441 RMVar_ID_32441 Human_SNP_ID_169409219 A-to-I Human chr3 - 195965941 195965941 195965941 CCGGGAAGTCAAGGCTCTGGCGAGCTGTGATCACACCATTACGCTCCAGCCCAGGTGACATAGCG CCGGGAAGTCAAGGCTCTGGCGAGCTGTGATCGCACCATTACGCTCCAGCCCAGGTGACATAGCG T C SDHAP1 Ensembl:ENSG00000185485 Pseudogene intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1295838493 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_335505 32442 RMVar_ID_32442 Human_SNP_ID_169409410 A-to-I Human chr3 - 195966472 195966472 195966472 TTTTGAGATGGAGTCTGACTGTCCCCCAGGCTAGAGTGCAGTGTTGCGATCTCAGCTCACTGCAA TTTTGAGATGGAGTCTGACTGTCCCCCAGGCTGGAGTGCAGTGTTGCGATCTCAGCTCACTGCAA T C SDHAP1 Ensembl:ENSG00000185485 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1403508144 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14979836 RMVar_hsa_circ_335505 32443 RMVar_ID_32443 Human_SNP_ID_169435640 A-to-I Human chr3 - 196052686 196052686 196052686 CTGTAATTCCAGTACTTTGGGAGGCCGAGGCAAGCGGATCACCTGAGGTCAGGAGTTCAAGACCA CTGTAATTCCAGTACTTTGGGAGGCCGAGGCATGCGGATCACCTGAGGTCAGGAGTTCAAGACCA T A TFRC Ensembl:ENSG00000072274 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1184941802 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_223845,RMVar_hsa_circ_111324,RMVar_hsa_circ_121595,RMVar_hsa_circ_128066,RMVar_hsa_circ_112376,RMVar_hsa_circ_81380,RMVar_hsa_circ_90811,RMVar_hsa_circ_223847,RMVar_hsa_circ_223849,RMVar_hsa_circ_80284,RMVar_hsa_circ_223848,RMVar_hsa_circ_223846,RMVar_hsa_circ_223843,RMVar_hsa_circ_223844 32444 RMVar_ID_32444 Human_SNP_ID_169435641 A-to-I Human chr3 - 196052686 196052686 196052686 CTGTAATTCCAGTACTTTGGGAGGCCGAGGCAAGCGGATCACCTGAGGTCAGGAGTTCAAGACCA CTGTAATTCCAGTACTTTGGGAGGCCGAGGCAGGCGGATCACCTGAGGTCAGGAGTTCAAGACCA T C TFRC Ensembl:ENSG00000072274 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1184941802 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_223845,RMVar_hsa_circ_111324,RMVar_hsa_circ_121595,RMVar_hsa_circ_128066,RMVar_hsa_circ_112376,RMVar_hsa_circ_81380,RMVar_hsa_circ_90811,RMVar_hsa_circ_223847,RMVar_hsa_circ_223849,RMVar_hsa_circ_80284,RMVar_hsa_circ_223848,RMVar_hsa_circ_223846,RMVar_hsa_circ_223843,RMVar_hsa_circ_223844 32445 RMVar_ID_32445 Human_SNP_ID_169435702 A-to-I Human chr3 - 196052891 196052891 196052891 CCAGGCCGGTCTCGAACTCCCAACCTCAAGTGATCCACCTGCCTTGGCCTCCCAAAGTGCTGGTA CCAGGCCGGTCTCGAACTCCCAACCTCAAGTGGTCCACCTGCCTTGGCCTCCCAAAGTGCTGGTA T C TFRC Ensembl:ENSG00000072274 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs564911971 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_223845,RMVar_hsa_circ_111324,RMVar_hsa_circ_121595,RMVar_hsa_circ_128066,RMVar_hsa_circ_112376,RMVar_hsa_circ_81380,RMVar_hsa_circ_90811,RMVar_hsa_circ_223847,RMVar_hsa_circ_223849,RMVar_hsa_circ_80284,RMVar_hsa_circ_223848,RMVar_hsa_circ_223846,RMVar_hsa_circ_223843,RMVar_hsa_circ_223844 32446 RMVar_ID_32446 Human_SNP_ID_169437904 A-to-I Human chr3 - 196060542 196060542 196060542 CACCCGTCTGGGCCTCCCAAAGTCCTGGGATTACAGGCGTGAGCCACCGTGCCCGGCCTAACTGC CACCCGTCTGGGCCTCCCAAAGTCCTGGGATTGCAGGCGTGAGCCACCGTGCCCGGCCTAACTGC T C TFRC Ensembl:ENSG00000072274 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1026210942 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25724635 RMVar_hsa_circ_67433,RMVar_hsa_circ_223845,RMVar_hsa_circ_111324,RMVar_hsa_circ_121595,RMVar_hsa_circ_128066,RMVar_hsa_circ_80284,RMVar_hsa_circ_223846,RMVar_hsa_circ_223843,RMVar_hsa_circ_223844,RMVar_hsa_circ_340292,RMVar_hsa_circ_363377,RMVar_hsa_circ_334288,RMVar_hsa_circ_308948,RMVar_hsa_circ_3131,RMVar_hsa_circ_22311,RMVar_hsa_circ_223854,RMVar_hsa_circ_65137,RMVar_hsa_circ_223853,RMVar_hsa_circ_377340,RMVar_hsa_circ_103045,RMVar_hsa_circ_340924,RMVar_hsa_circ_223855,RMVar_hsa_circ_223856,RMVar_hsa_circ_343677,RMVar_hsa_circ_367866,RMVar_hsa_circ_341777,RMVar_hsa_circ_310545,RMVar_hsa_circ_321932,RMVar_hsa_circ_59092,RMVar_hsa_circ_106356,RMVar_hsa_circ_34129,RMVar_hsa_circ_103477,RMVar_hsa_circ_223857,RMVar_hsa_circ_223859,RMVar_hsa_circ_223860,RMVar_hsa_circ_223858,RMVar_hsa_circ_223863,RMVar_hsa_circ_126589,RMVar_hsa_circ_370056,RMVar_hsa_circ_370440,RMVar_hsa_circ_223865,RMVar_hsa_circ_21161,RMVar_hsa_circ_223866,RMVar_hsa_circ_223864 32447 RMVar_ID_32447 Human_SNP_ID_169438454 A-to-I Human chr3 - 196062489 196062489 196062489 TGCTCTTGTCGCCCAGGCTGGAGTGCAATGGCACGATCTCGGCTCACTGCAACCTCTGTCTCCCA TGCTCTTGTCGCCCAGGCTGGAGTGCAATGGCTCGATCTCGGCTCACTGCAACCTCTGTCTCCCA T A TFRC Ensembl:ENSG00000072274 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1238779799 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67433,RMVar_hsa_circ_223845,RMVar_hsa_circ_111324,RMVar_hsa_circ_121595,RMVar_hsa_circ_128066,RMVar_hsa_circ_80284,RMVar_hsa_circ_223846,RMVar_hsa_circ_223843,RMVar_hsa_circ_223844,RMVar_hsa_circ_340292,RMVar_hsa_circ_363377,RMVar_hsa_circ_334288,RMVar_hsa_circ_308948,RMVar_hsa_circ_3131,RMVar_hsa_circ_22311,RMVar_hsa_circ_223854,RMVar_hsa_circ_65137,RMVar_hsa_circ_223853,RMVar_hsa_circ_377340,RMVar_hsa_circ_103045,RMVar_hsa_circ_340924,RMVar_hsa_circ_223855,RMVar_hsa_circ_223856,RMVar_hsa_circ_343677,RMVar_hsa_circ_367866,RMVar_hsa_circ_341777,RMVar_hsa_circ_310545,RMVar_hsa_circ_321932,RMVar_hsa_circ_59092,RMVar_hsa_circ_106356,RMVar_hsa_circ_34129,RMVar_hsa_circ_103477,RMVar_hsa_circ_223857,RMVar_hsa_circ_223859,RMVar_hsa_circ_223860,RMVar_hsa_circ_223858,RMVar_hsa_circ_223863,RMVar_hsa_circ_126589,RMVar_hsa_circ_370056,RMVar_hsa_circ_370440,RMVar_hsa_circ_223865,RMVar_hsa_circ_21161,RMVar_hsa_circ_223866,RMVar_hsa_circ_223864 32448 RMVar_ID_32448 Human_SNP_ID_169440451 A-to-I Human chr3 - 196069082 196069082 196069082 AAAAAGTGGCAGGGCTCACACCTGTAATCCCAACACTTTAGGAGGCTGAGGTGGGAGGACTGCTT AAAAAGTGGCAGGGCTCACACCTGTAATCCCAGCACTTTAGGAGGCTGAGGTGGGAGGACTGCTT T C TFRC Ensembl:ENSG00000072274 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1183239478 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14761225 RMVar_hsa_circ_67433,RMVar_hsa_circ_121595,RMVar_hsa_circ_80284,RMVar_hsa_circ_223843,RMVar_hsa_circ_223844,RMVar_hsa_circ_334288,RMVar_hsa_circ_308948,RMVar_hsa_circ_4933,RMVar_hsa_circ_3131,RMVar_hsa_circ_223854,RMVar_hsa_circ_65137,RMVar_hsa_circ_343677,RMVar_hsa_circ_341777,RMVar_hsa_circ_321932,RMVar_hsa_circ_59092,RMVar_hsa_circ_46360,RMVar_hsa_circ_103477,RMVar_hsa_circ_223857,RMVar_hsa_circ_223858,RMVar_hsa_circ_223863,RMVar_hsa_circ_126589,RMVar_hsa_circ_370056,RMVar_hsa_circ_370440,RMVar_hsa_circ_341688,RMVar_hsa_circ_223865,RMVar_hsa_circ_21161,RMVar_hsa_circ_223866,RMVar_hsa_circ_223864,RMVar_hsa_circ_58492,RMVar_hsa_circ_337880,RMVar_hsa_circ_94702,RMVar_hsa_circ_223867,RMVar_hsa_circ_223868,RMVar_hsa_circ_278750,RMVar_hsa_circ_223869,RMVar_hsa_circ_23053,RMVar_hsa_circ_329308,RMVar_hsa_circ_373516,RMVar_hsa_circ_83398,RMVar_hsa_circ_86947,RMVar_hsa_circ_35376,RMVar_hsa_circ_223871,RMVar_hsa_circ_223872,RMVar_hsa_circ_297912,RMVar_hsa_circ_115479,RMVar_hsa_circ_223875,RMVar_hsa_circ_70073,RMVar_hsa_circ_223874 32449 RMVar_ID_32449 Human_SNP_ID_169442338 A-to-I Human chr3 - 196075314 196075314 196075314 ATTGTCATATACCCGGTTCAGCCTGGCTCGGCAAGTAGATGGCGATAACAGTCATGTGGAGATGA ATTGTCATATACCCGGTTCAGCCTGGCTCGGCGAGTAGATGGCGATAACAGTCATGTGGAGATGA T C TFRC Ensembl:ENSG00000072274 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs761118538 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_66642,Human_RBP_ID_597868,Human_RBP_ID_782868,Human_RBP_ID_834688,Human_RBP_ID_938254,Human_RBP_ID_3964555,Human_RBP_ID_4756923,Human_RBP_ID_5530770,Human_RBP_ID_14761424,Human_RBP_ID_17194696,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 32450 RMVar_ID_32450 Human_SNP_ID_169442548 A-to-I Human chr3 - 196075925 196075925 196075925 GGGGATTTCACCATGTTGGTCAGGCTTGTCTCAAACTTCTGACCATAAATGATCTGTGTGCCTCG GGGGATTTCACCATGTTGGTCAGGCTTGTCTCGAACTTCTGACCATAAATGATCTGTGTGCCTCG T C TFRC Ensembl:ENSG00000072274 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1283016980 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121595,RMVar_hsa_circ_223843,RMVar_hsa_circ_308948,RMVar_hsa_circ_223854,RMVar_hsa_circ_341777,RMVar_hsa_circ_370440,RMVar_hsa_circ_341688,RMVar_hsa_circ_223866,RMVar_hsa_circ_223867,RMVar_hsa_circ_329308,RMVar_hsa_circ_297912,RMVar_hsa_circ_70073,RMVar_hsa_circ_48394,RMVar_hsa_circ_279359,RMVar_hsa_circ_315825,RMVar_hsa_circ_223877,RMVar_hsa_circ_223880,RMVar_hsa_circ_299304,RMVar_hsa_circ_223882,RMVar_hsa_circ_223883,RMVar_hsa_circ_311286 32451 RMVar_ID_32451 Human_SNP_ID_169442575 A-to-I Human chr3 - 196075990 196075990 196075990 GAGATTACAGGCGTGCGACACCATGCCCAGCTAGTGGTTTTTTTTTTTTTGAATTTTTAGTGAGA GAGATTACAGGCGTGCGACACCATGCCCAGCTGGTGGTTTTTTTTTTTTTGAATTTTTAGTGAGA T C TFRC Ensembl:ENSG00000072274 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1198670197 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121595,RMVar_hsa_circ_223843,RMVar_hsa_circ_308948,RMVar_hsa_circ_223854,RMVar_hsa_circ_341777,RMVar_hsa_circ_370440,RMVar_hsa_circ_341688,RMVar_hsa_circ_223866,RMVar_hsa_circ_223867,RMVar_hsa_circ_329308,RMVar_hsa_circ_297912,RMVar_hsa_circ_70073,RMVar_hsa_circ_48394,RMVar_hsa_circ_279359,RMVar_hsa_circ_315825,RMVar_hsa_circ_223877,RMVar_hsa_circ_223880,RMVar_hsa_circ_299304,RMVar_hsa_circ_223882,RMVar_hsa_circ_223883,RMVar_hsa_circ_311286 32452 RMVar_ID_32452 Human_SNP_ID_169443229 A-to-I Human chr3 - 196078509 196078509 196078509 GGGATTACAGGTGCCCACCACCACGCCCATCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCA GGGATTACAGGTGCCCACCACCACGCCCATCTGATTTTTGTATTTTTAGTAGAGATGGGGTTTCA T C TFRC Ensembl:ENSG00000072274 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1319911046 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_157103 32453 RMVar_ID_32453 Human_SNP_ID_169443350 A-to-I Human chr3 - 196078872 196078872 196078872 CTACTCGGAGTCTGAGGTGGGAAAATGGCTTGAACCCGGGAGGGGGAGGTTGCAGTGAGCCGAGA CTACTCGGAGTCTGAGGTGGGAAAATGGCTTGTACCCGGGAGGGGGAGGTTGCAGTGAGCCGAGA T A TFRC Ensembl:ENSG00000072274 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs899957500 Functional Loss SNV dbSNP153 33..33 33 - - - 32454 RMVar_ID_32454 Human_SNP_ID_169443366 A-to-I Human chr3 - 196078930 196078930 196078930 GTCTCTACTAAAAATACAAAAATTAGCTGGGCATGGTGGTGGGCACCTGTAATCCCAGCTACTCG GTCTCTACTAAAAATACAAAAATTAGCTGGGCGTGGTGGTGGGCACCTGTAATCCCAGCTACTCG T C TFRC Ensembl:ENSG00000072274 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1197271201 Functional Loss SNV dbSNP153 33..33 33 - - - 32455 RMVar_ID_32455 Human_SNP_ID_169443504 A-to-I Human chr3 - 196079395 196079395 196079395 TTTGGTCAGGCTAGTCTCAAACTCTCAACCTCAGGTGATCTGCTCGCCTCGGCCTCCCAAAGTGT TTTGGTCAGGCTAGTCTCAAACTCTCAACCTCTGGTGATCTGCTCGCCTCGGCCTCCCAAAGTGT T A TFRC Ensembl:ENSG00000072274 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1299711608 Functional Loss SNV dbSNP153 33..33 33 - - - 32456 RMVar_ID_32456 Human_SNP_ID_169443531 A-to-I Human chr3 - 196079486 196079486 196079486 CCTCAGCCTCCCCAGTAGCTGGGATTACAGGCATGCGCCACCATGCCCGGCTAATTTTGTATTTT CCTCAGCCTCCCCAGTAGCTGGGATTACAGGCTTGCGCCACCATGCCCGGCTAATTTTGTATTTT T A TFRC Ensembl:ENSG00000072274 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs558133079 Functional Loss SNV dbSNP153 33..33 33 - - - 32457 RMVar_ID_32457 Human_SNP_ID_169443551 A-to-I Human chr3 - 196079577 196079577 196079577 AGTTTCACGCTTGTTGCCCAGGCTGTAGTGCAATGGTGTGATCTCGGCTCCCTGCAACCTCCACC AGTTTCACGCTTGTTGCCCAGGCTGTAGTGCAGTGGTGTGATCTCGGCTCCCTGCAACCTCCACC T C TFRC Ensembl:ENSG00000072274 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1196082289 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14761464 32458 RMVar_ID_32458 Human_SNP_ID_169443562 A-to-I Human chr3 - 196079611 196079611 196079611 CTTAGATTATTATTTATTTATTTATTTTTGACAGAGTTTCACGCTTGTTGCCCAGGCTGTAGTGC CTTAGATTATTATTTATTTATTTATTTTTGACGGAGTTTCACGCTTGTTGCCCAGGCTGTAGTGC T C TFRC Ensembl:ENSG00000072274 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1401450188 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14761465 32459 RMVar_ID_32459 Human_SNP_ID_169484759 A-to-I Human chr3 - 196224154 196224154 196224154 CAAATGTTAAATAAAAACATAGAGAAAGGGCTAGGCACAGTGGCTCATGCCTGTAATCCCAGCAC CAAATGTTAAATAAAAACATAGAGAAAGGGCTGGGCACAGTGGCTCATGCCTGTAATCCCAGCAC T C PCYT1A Ensembl:ENSG00000161217 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs931222523 Functional Loss SNV dbSNP153 33..33 33 - - - 32460 RMVar_ID_32460 Human_SNP_ID_169489911 A-to-I Human chr3 - 196243138 196243138 196243138 TATTTTTAGTAGAGACGGGGTTTCACCATGTTAGCCACGTTAGTCTTGAACTCCTGACCTCGTGA TATTTTTAGTAGAGACGGGGTTTCACCATGTTTGCCACGTTAGTCTTGAACTCCTGACCTCGTGA T A PCYT1A Ensembl:ENSG00000161217 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031358520 Functional Loss SNV dbSNP153 33..33 33 - - - 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 32461 RMVar_ID_32461 Human_SNP_ID_169489912 A-to-I Human chr3 - 196243138 196243138 196243138 TATTTTTAGTAGAGACGGGGTTTCACCATGTTAGCCACGTTAGTCTTGAACTCCTGACCTCGTGA TATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCACGTTAGTCTTGAACTCCTGACCTCGTGA T C PCYT1A Ensembl:ENSG00000161217 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031358520 Functional Loss SNV dbSNP153 33..33 33 - - - 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 32462 RMVar_ID_32462 Human_SNP_ID_169493758 A-to-I Human chr3 - 196256733 196256733 196256733 GAGTTCGAGACCAGCCTGGTTAACATGGTGAAACCCCTTCTCTACTAAAAATACAAAAGTTAGCT GAGTTCGAGACCAGCCTGGTTAACATGGTGAAGCCCCTTCTCTACTAAAAATACAAAAGTTAGCT T C PCYT1A,AC069257.4 Ensembl:ENSG00000161217,Ensembl:ENSG00000272741 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1342855192 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112875,RMVar_hsa_circ_223887,RMVar_hsa_circ_223894,RMVar_hsa_circ_92469 32463 RMVar_ID_32463 Human_SNP_ID_169496494 A-to-I Human chr3 - 196268695 196268695 196268695 TGCCTCTTGGGTTCAAGTGATTTCCCTGCCTCAGCCTCCCAAGTGGCTGGGATTGCAGGTGCCCA TGCCTCTTGGGTTCAAGTGATTTCCCTGCCTCGGCCTCCCAAGTGGCTGGGATTGCAGGTGCCCA T C PCYT1A,AC069257.4 Ensembl:ENSG00000161217,Ensembl:ENSG00000272741 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1266169612 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112875,RMVar_hsa_circ_223887,RMVar_hsa_circ_472,RMVar_hsa_circ_223894,RMVar_hsa_circ_92469,RMVar_hsa_circ_300959,RMVar_hsa_circ_13538 32464 RMVar_ID_32464 Human_SNP_ID_169501800 A-to-I Human chr3 - 196291607 196291607 196291607 TGGTATGGTGGCAGGCACCTGTGGTCCTAGCTACTCTGGAGGCTGAGGTAGAAGGATTGCCTGAG TGGTATGGTGGCAGGCACCTGTGGTCCTAGCTGCTCTGGAGGCTGAGGTAGAAGGATTGCCTGAG T C TCTEX1D2,AC069257.4 Ensembl:ENSG00000213123,Ensembl:ENSG00000272741 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202977878 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_223895 32465 RMVar_ID_32465 Human_SNP_ID_169504177 A-to-I Human chr3 - 196302024 196302024 196302024 CGACTCATCGCAACCTTCACCTCCTGGGTTTAAGCGATTCTCGTGCTTCAGCCTCCCAAGTAGCA CGACTCATCGCAACCTTCACCTCCTGGGTTTACGCGATTCTCGTGCTTCAGCCTCCCAAGTAGCA T G TCTEX1D2,AC069257.4 Ensembl:ENSG00000213123,Ensembl:ENSG00000272741 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928849119 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27715,RMVar_hsa_circ_22618 32466 RMVar_ID_32466 Human_SNP_ID_169504668 A-to-I Human chr3 - 196304195 196304195 196304195 CTGGGAGGTGGAGGTTGCAGTGAGCTGAGATCACGCCACTGCACTCCAGCCTGGGGAACAGAGTG CTGGGAGGTGGAGGTTGCAGTGAGCTGAGATCGCGCCACTGCACTCCAGCCTGGGGAACAGAGTG T C TCTEX1D2,AC069257.4 Ensembl:ENSG00000213123,Ensembl:ENSG00000272741 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs993902890 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27715,RMVar_hsa_circ_22618 32467 RMVar_ID_32467 Human_SNP_ID_169504880 A-to-I Human chr3 - 196305011 196305011 196305011 GGGCATGGTGGCACACGCCTGTGGTCCCAGCTACTTGAGAGACTGAGGTGGGAGGACCTCTTGAG GGGCATGGTGGCACACGCCTGTGGTCCCAGCTGCTTGAGAGACTGAGGTGGGAGGACCTCTTGAG T C TCTEX1D2,AC069257.4 Ensembl:ENSG00000213123,Ensembl:ENSG00000272741 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs891156247 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27715,RMVar_hsa_circ_22618 32468 RMVar_ID_32468 Human_SNP_ID_169505011 A-to-I Human chr3 - 196305692 196305692 196305692 GGTTCAAGTGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCGCTCACCACCACGC GGTTCAAGTGATTCTCCTGCCTCAGCCTCCTGCGTAGCTGGGATTACAGGCGCTCACCACCACGC T G TCTEX1D2,AC069257.4 Ensembl:ENSG00000213123,Ensembl:ENSG00000272741 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs144978923 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_530466,Human_Splice_Rec_530467 RMVar_hsa_circ_27715,RMVar_hsa_circ_22618 32469 RMVar_ID_32469 Human_SNP_ID_169505070 A-to-I Human chr3 - 196305966 196305966 196305966 GTGGCTATTCACAGATGTGATCATAACACACTACAGACTAGAACTCCTGGGCTCAAGTGATCCTC GTGGCTATTCACAGATGTGATCATAACACACTGCAGACTAGAACTCCTGGGCTCAAGTGATCCTC T C TCTEX1D2,AC069257.4 Ensembl:ENSG00000213123,Ensembl:ENSG00000272741 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs954621291 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27715,RMVar_hsa_circ_22618 32470 RMVar_ID_32470 Human_SNP_ID_169507668 A-to-I Human chr3 - 196316000 196316000 196316000 CTCTCCATCTTTAAACAAAGGACATTGGGGCCAGGTGTGGTGGCTCACGCCTACAATCCCAACAC CTCTCCATCTTTAAACAAAGGACATTGGGGCCCGGTGTGGTGGCTCACGCCTACAATCCCAACAC T G TCTEX1D2,AC069257.4 Ensembl:ENSG00000213123,Ensembl:ENSG00000272741 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749704491 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15285,RMVar_hsa_circ_22618,RMVar_hsa_circ_223898 32471 RMVar_ID_32471 Human_SNP_ID_169509020 A-to-I Human chr3 - 196318957 196318957 196318957 AAATTAGCCGGTCGTGGTGGGGCGCGCCTGTAATCCCTGCTGCTTGGGAGGCTGAGGCAGAATTG AAATTAGCCGGTCGTGGTGGGGCGCGCCTGTATTCCCTGCTGCTTGGGAGGCTGAGGCAGAATTG T A TM4SF19-TCTEX1D2 Ensembl:ENSG00000273331 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1216871507 Functional Loss SNV dbSNP153 33..33 33 - - - 32472 RMVar_ID_32472 Human_SNP_ID_169509049 A-to-I Human chr3 - 196319050 196319050 196319050 CGGGAGACCGAGGTGGGCGATCACCTGAGGTCAGGAGTTGGAGACCAGCCTGGCCAATATGGTGA CGGGAGACCGAGGTGGGCGATCACCTGAGGTCGGGAGTTGGAGACCAGCCTGGCCAATATGGTGA T C TM4SF19-TCTEX1D2 Ensembl:ENSG00000273331 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs990183054 Functional Loss SNV dbSNP153 33..33 33 - - - 32473 RMVar_ID_32473 Human_SNP_ID_169509279 A-to-I Human chr3 - 196319907 196319907 196319907 CACAATGTTAGCCAGGATGGTCTTGATCTCCTAACCTCATGATCCGCCCGCCTCGGCCTCCCAAA CACAATGTTAGCCAGGATGGTCTTGATCTCCTGACCTCATGATCCGCCCGCCTCGGCCTCCCAAA T C TM4SF19,TM4SF19-TCTEX1D2 Ensembl:ENSG00000145107,Ensembl:ENSG00000273331 Protein coding,Protein coding CDS,intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1159704043 Functional Loss SNV dbSNP153 33..33 33 - - - 32474 RMVar_ID_32474 Human_SNP_ID_169509292 A-to-I Human chr3 - 196319930 196319930 196319930 TATTTTTAGTAGAGACCGGGTTTCACAATGTTAGCCAGGATGGTCTTGATCTCCTAACCTCATGA TATTTTTAGTAGAGACCGGGTTTCACAATGTTGGCCAGGATGGTCTTGATCTCCTAACCTCATGA T C TM4SF19,TM4SF19-TCTEX1D2 Ensembl:ENSG00000145107,Ensembl:ENSG00000273331 Protein coding,Protein coding CDS,intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs937723608 Functional Loss SNV dbSNP153 33..33 33 - - - 32475 RMVar_ID_32475 Human_SNP_ID_169509354 A-to-I Human chr3 - 196320055 196320055 196320055 GGAGTGCAGTGGTGTGATCTCGGCTCACTGCAAGCTCCGACTCCCTGGTTCAAGCAATTCTCCTG GGAGTGCAGTGGTGTGATCTCGGCTCACTGCACGCTCCGACTCCCTGGTTCAAGCAATTCTCCTG T G TM4SF19,TM4SF19-TCTEX1D2 Ensembl:ENSG00000145107,Ensembl:ENSG00000273331 Protein coding,Protein coding CDS,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1165803526 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_530496 32476 RMVar_ID_32476 Human_SNP_ID_169509853 A-to-I Human chr3 - 196321632 196321632 196321632 TTGTACTTTTAGTAGAGATGGGTTTTCACCATATTGGCCAGGCTGGTCTTGAACTCCTGACCTTG TTGTACTTTTAGTAGAGATGGGTTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGACCTTG T C TM4SF19,TM4SF19-TCTEX1D2 Ensembl:ENSG00000145107,Ensembl:ENSG00000273331 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432014331 Functional Loss SNV dbSNP153 33..33 33 - - - 32477 RMVar_ID_32477 Human_SNP_ID_169510101 A-to-I Human chr3 - 196322643 196322643 196322643 TTAGTAATTAAGGTTAAATGAGACTGGGCGCAATGGCTCACACCTGTAATCTGAGCACTTTGGGA TTAGTAATTAAGGTTAAATGAGACTGGGCGCAGTGGCTCACACCTGTAATCTGAGCACTTTGGGA T C TM4SF19,TM4SF19-TCTEX1D2 Ensembl:ENSG00000145107,Ensembl:ENSG00000273331 Protein coding,Protein coding intron,intron GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs767184219 Functional Loss SNV dbSNP153 33..33 33 - - - 32478 RMVar_ID_32478 Human_SNP_ID_169510236 A-to-I Human chr3 - 196323170 196323170 196323170 ATTGCCCAGTCTGGTCTTGAACTCCTGACCTCAAGTGATCCTCCCACCTTGGTCTCCCAAAGCGC ATTGCCCAGTCTGGTCTTGAACTCCTGACCTCGAGTGATCCTCCCACCTTGGTCTCCCAAAGCGC T C TM4SF19,TM4SF19-TCTEX1D2 Ensembl:ENSG00000145107,Ensembl:ENSG00000273331 Protein coding,Protein coding intron,intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs561469847 Functional Loss SNV dbSNP153 33..33 33 - - - 32479 RMVar_ID_32479 Human_SNP_ID_169510245 A-to-I Human chr3 - 196323204 196323204 196323204 TTTTAAATTTTCTGTAGAGAGGGAGTCTCGCTATATTGCCCAGTCTGGTCTTGAACTCCTGACCT TTTTAAATTTTCTGTAGAGAGGGAGTCTCGCTGTATTGCCCAGTCTGGTCTTGAACTCCTGACCT T C TM4SF19,TM4SF19-TCTEX1D2 Ensembl:ENSG00000145107,Ensembl:ENSG00000273331 Protein coding,Protein coding intron,intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs1261596915 Functional Loss SNV dbSNP153 33..33 33 - - - 32480 RMVar_ID_32480 Human_SNP_ID_169510265 A-to-I Human chr3 - 196323303 196323302 196323303 TAGCTTACTGTAACCTACAACCCATGCACTCAAGCGATCCTCCTGCCTTAGCCTCCGAGTAGCTG TAGCTTACTGTAACCTACAACCCATGCACTCA_GCGATCCTCCTGCCTTAGCCTCCGAGTAGCTG CT C TM4SF19,TM4SF19-TCTEX1D2 Ensembl:ENSG00000145107,Ensembl:ENSG00000273331 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215617387 Functional Loss DEL dbSNP153 33..33 33 - - - 32481 RMVar_ID_32481 Human_SNP_ID_169512429 A-to-I Human chr3 - 196331824 196331824 196331824 GCCAAGGAGTTTGAGACCAGCCTGGGCCACATAAGGAGACCTCACCTCTATTACATTTTTTTTTC GCCAAGGAGTTTGAGACCAGCCTGGGCCACATCAGGAGACCTCACCTCTATTACATTTTTTTTTC T G TM4SF19,TM4SF19-TCTEX1D2 Ensembl:ENSG00000145107,Ensembl:ENSG00000273331 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1010527408 Functional Loss SNV dbSNP153 33..33 33 - - - 32482 RMVar_ID_32482 Human_SNP_ID_169518312 A-to-I Human chr3 - 196352405 196352405 196352405 CCCATCTCTACTGAAAAATACAAAAATTAGCCAGGCATGGTGGCTGTCTGTAATCCCAGCTAATG CCCATCTCTACTGAAAAATACAAAAATTAGCCGGGCATGGTGGCTGTCTGTAATCCCAGCTAATG T C UBXN7 Ensembl:ENSG00000163960 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1165174458 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_597928,Human_RBP_ID_26511497 32483 RMVar_ID_32483 Human_SNP_ID_169518339 A-to-I Human chr3 - 196352512 196352512 196352512 GCCAGGTGTGGTGGCTCATGCCTGTAATCCCAATATTTTGGGAGGCCGAGGTGGGTGGATCACCT GCCAGGTGTGGTGGCTCATGCCTGTAATCCCAGTATTTTGGGAGGCCGAGGTGGGTGGATCACCT T C UBXN7 Ensembl:ENSG00000163960 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1277441564 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14762162 32484 RMVar_ID_32484 Human_SNP_ID_169518401 A-to-I Human chr3 - 196352809 196352809 196352809 TTTTGCATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGATGGTCTCGATCTCTTGATCT TTTTGCATTTTTAGTAGAGACAGGGTTTCACCTTGTTGGCCAGGATGGTCTCGATCTCTTGATCT T A UBXN7 Ensembl:ENSG00000163960 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1460702691 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4736499 32485 RMVar_ID_32485 Human_SNP_ID_169521576 A-to-I Human chr3 - 196365543 196365543 196365543 TTACGGAACCAGCTGGGGTGTGGCATGTGCCTATAGTCCCATCTGCTTGGCAGGAATATTGCTTG TTACGGAACCAGCTGGGGTGTGGCATGTGCCTGTAGTCCCATCTGCTTGGCAGGAATATTGCTTG T C UBXN7 Ensembl:ENSG00000163960 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs540472761 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7176054 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 32486 RMVar_ID_32486 Human_SNP_ID_169523291 A-to-I Human chr3 - 196372480 196372480 196372480 AAAATCAGCCAGGCGTGTTGGGGCACGCCTTTAATCCCAACTACTTGGGAGGCTGCGGCGGGAGA AAAATCAGCCAGGCGTGTTGGGGCACGCCTTTTATCCCAACTACTTGGGAGGCTGCGGCGGGAGA T A UBXN7 Ensembl:ENSG00000163960 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1410500417 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27464,RMVar_hsa_circ_277841,RMVar_hsa_circ_223903,RMVar_hsa_circ_368072,RMVar_hsa_circ_337556,RMVar_hsa_circ_91179,RMVar_hsa_circ_20785,RMVar_hsa_circ_223906,RMVar_hsa_circ_223907,RMVar_hsa_circ_319207,RMVar_hsa_circ_293626,RMVar_hsa_circ_275439,RMVar_hsa_circ_223910,RMVar_hsa_circ_223912,RMVar_hsa_circ_324453,RMVar_hsa_circ_369763,RMVar_hsa_circ_223911,RMVar_hsa_circ_364759,RMVar_hsa_circ_273973,RMVar_hsa_circ_223915,RMVar_hsa_circ_223916 32487 RMVar_ID_32487 Human_SNP_ID_169530076 A-to-I Human chr3 - 196397682 196397682 196397682 TGAGCCCCAGGAGTTCTTGGCTGTAGGGCCCTATGCTGATTGGGTGTCTGCACTAAGTTCGGAAT TGAGCCCCAGGAGTTCTTGGCTGTAGGGCCCTTTGCTGATTGGGTGTCTGCACTAAGTTCGGAAT T A RN7SL434P,UBXN7 Ensembl:ENSG00000241868,Ensembl:ENSG00000163960 Other,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1415253932 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14762526 RMVar_hsa_circ_27464,RMVar_hsa_circ_277841,RMVar_hsa_circ_223903,RMVar_hsa_circ_337556,RMVar_hsa_circ_91179,RMVar_hsa_circ_223918,RMVar_hsa_circ_20785,RMVar_hsa_circ_223906,RMVar_hsa_circ_223907,RMVar_hsa_circ_319207,RMVar_hsa_circ_275439,RMVar_hsa_circ_223910,RMVar_hsa_circ_324453,RMVar_hsa_circ_223911,RMVar_hsa_circ_273973,RMVar_hsa_circ_269883,RMVar_hsa_circ_223916,RMVar_hsa_circ_280413,RMVar_hsa_circ_223917,RMVar_hsa_circ_370441,RMVar_hsa_circ_223922 32488 RMVar_ID_32488 Human_SNP_ID_169530575 A-to-I Human chr3 - 196399616 196399616 196399616 AGACAACATAGGAAGACTCTTATCTCTACAAAAAATAAAAATAAATTCGTTAGGCATGGTGGCAC AGACAACATAGGAAGACTCTTATCTCTACAAAGAATAAAAATAAATTCGTTAGGCATGGTGGCAC T C UBXN7 Ensembl:ENSG00000163960 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs987380572 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18002563 RMVar_hsa_circ_27464,RMVar_hsa_circ_277841,RMVar_hsa_circ_223903,RMVar_hsa_circ_337556,RMVar_hsa_circ_91179,RMVar_hsa_circ_223918,RMVar_hsa_circ_20785,RMVar_hsa_circ_223906,RMVar_hsa_circ_223907,RMVar_hsa_circ_319207,RMVar_hsa_circ_275439,RMVar_hsa_circ_223910,RMVar_hsa_circ_324453,RMVar_hsa_circ_223911,RMVar_hsa_circ_273973,RMVar_hsa_circ_269883,RMVar_hsa_circ_223916,RMVar_hsa_circ_280413,RMVar_hsa_circ_223917,RMVar_hsa_circ_370441,RMVar_hsa_circ_223922 32489 RMVar_ID_32489 Human_SNP_ID_169530576 A-to-I Human chr3 - 196399616 196399616 196399616 AGACAACATAGGAAGACTCTTATCTCTACAAAAAATAAAAATAAATTCGTTAGGCATGGTGGCAC AGACAACATAGGAAGACTCTTATCTCTACAAACAATAAAAATAAATTCGTTAGGCATGGTGGCAC T G UBXN7 Ensembl:ENSG00000163960 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs987380572 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18002563 RMVar_hsa_circ_27464,RMVar_hsa_circ_277841,RMVar_hsa_circ_223903,RMVar_hsa_circ_337556,RMVar_hsa_circ_91179,RMVar_hsa_circ_223918,RMVar_hsa_circ_20785,RMVar_hsa_circ_223906,RMVar_hsa_circ_223907,RMVar_hsa_circ_319207,RMVar_hsa_circ_275439,RMVar_hsa_circ_223910,RMVar_hsa_circ_324453,RMVar_hsa_circ_223911,RMVar_hsa_circ_273973,RMVar_hsa_circ_269883,RMVar_hsa_circ_223916,RMVar_hsa_circ_280413,RMVar_hsa_circ_223917,RMVar_hsa_circ_370441,RMVar_hsa_circ_223922 32490 RMVar_ID_32490 Human_SNP_ID_169530661 A-to-I Human chr3 - 196400007 196400007 196400007 GATGTCGAGCTTAGTGTAGACACCTGACTGGCATAGCACACTACAGGCCAGAACTCTTAGGCTCA GATGTCGAGCTTAGTGTAGACACCTGACTGGCGTAGCACACTACAGGCCAGAACTCTTAGGCTCA T C UBXN7 Ensembl:ENSG00000163960 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048012486 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14762542 RMVar_hsa_circ_27464,RMVar_hsa_circ_277841,RMVar_hsa_circ_223903,RMVar_hsa_circ_337556,RMVar_hsa_circ_91179,RMVar_hsa_circ_223918,RMVar_hsa_circ_20785,RMVar_hsa_circ_223906,RMVar_hsa_circ_223907,RMVar_hsa_circ_319207,RMVar_hsa_circ_275439,RMVar_hsa_circ_223910,RMVar_hsa_circ_324453,RMVar_hsa_circ_223911,RMVar_hsa_circ_273973,RMVar_hsa_circ_269883,RMVar_hsa_circ_223916,RMVar_hsa_circ_280413,RMVar_hsa_circ_223917,RMVar_hsa_circ_370441,RMVar_hsa_circ_223922 32491 RMVar_ID_32491 Human_SNP_ID_169534261 A-to-I Human chr3 - 196413255 196413255 196413255 CGGCTCACTGCAACCTCTGCCTCCTGGGTTCAAGCGGTTCTCCTCCCTCAGCCTGCCCAGTAGCT CGGCTCACTGCAACCTCTGCCTCCTGGGTTCAGGCGGTTCTCCTCCCTCAGCCTGCCCAGTAGCT T C UBXN7 Ensembl:ENSG00000163960 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1216205189 Functional Loss SNV dbSNP153 33..33 33 - - - 32492 RMVar_ID_32492 Human_SNP_ID_169552960 A-to-I Human chr3 - 196477849 196477849 196477849 GGACTCCTGGCCTCAAACGATCCTCCCACCTCAGCCTCCCAAAGTGTTAGAATTACAGGCATGAA GGACTCCTGGCCTCAAACGATCCTCCCACCTCGGCCTCCCAAAGTGTTAGAATTACAGGCATGAA T C RNF168 Ensembl:ENSG00000163961 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs189037670 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17574217 RMVar_hsa_circ_118002,RMVar_hsa_circ_264962,RMVar_hsa_circ_223927,RMVar_hsa_circ_223924,RMVar_hsa_circ_223926,RMVar_hsa_circ_223928,RMVar_hsa_circ_367451,RMVar_hsa_circ_378721,RMVar_hsa_circ_329243 32493 RMVar_ID_32493 Human_SNP_ID_169552961 A-to-I Human chr3 - 196477849 196477849 196477849 GGACTCCTGGCCTCAAACGATCCTCCCACCTCAGCCTCCCAAAGTGTTAGAATTACAGGCATGAA GGACTCCTGGCCTCAAACGATCCTCCCACCTCCGCCTCCCAAAGTGTTAGAATTACAGGCATGAA T G RNF168 Ensembl:ENSG00000163961 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs189037670 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17574217 RMVar_hsa_circ_118002,RMVar_hsa_circ_264962,RMVar_hsa_circ_223927,RMVar_hsa_circ_223924,RMVar_hsa_circ_223926,RMVar_hsa_circ_223928,RMVar_hsa_circ_367451,RMVar_hsa_circ_378721,RMVar_hsa_circ_329243 32494 RMVar_ID_32494 Human_SNP_ID_169554917 A-to-I Human chr3 - 196484375 196484343 196484376 GGTCAGGAAATCGAGACCATCCTGGCTAACACAGTGAAACCCCATCTCTACTAAAAAAAATACAA GGTCAGGAAATCGAGACCATCCTGGCTAACA_________________________________A TTGTATTTTTTTTAGTAGAGATGGGGTTTCACTG T RNF168 Ensembl:ENSG00000163961 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1164202503 Functional Loss DEL dbSNP153 32..64 33 - - - 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 32495 RMVar_ID_32495 Human_SNP_ID_169555237 A-to-I Human chr3 - 196485475 196485475 196485475 TTAACTTTTTTTTTTTTTGAGACAAGAGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTAGTGCA TTAACTTTTTTTTTTTTTGAGACAAGAGTCTCTCTCTGTCACCCAGGCTGGAGTGCAGTAGTGCA T A RNF168 Ensembl:ENSG00000163961 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1021344119 Functional Loss SNV dbSNP153 33..33 33 - - - 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 32496 RMVar_ID_32496 Human_SNP_ID_169555621 A-to-I Human chr3 - 196486939 196486939 196486939 TGATCCTTCCAACCTCCCGAGTAGCTGGGACTACAGGCTGGCACTACCATGCCTGGCTACTTTTT TGATCCTTCCAACCTCCCGAGTAGCTGGGACTGCAGGCTGGCACTACCATGCCTGGCTACTTTTT T C RNF168 Ensembl:ENSG00000163961 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049518507 Functional Loss SNV dbSNP153 33..33 33 - - - 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 32497 RMVar_ID_32497 Human_SNP_ID_169555652 A-to-I Human chr3 - 196487011 196487011 196487011 TTACTCTGTCATGCAGGTTGGAGTGCAGTGGCACAATCACGACTCACTGCAGCCTCGACGGCCGG TTACTCTGTCATGCAGGTTGGAGTGCAGTGGCGCAATCACGACTCACTGCAGCCTCGACGGCCGG T C RNF168 Ensembl:ENSG00000163961 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs990838310 Functional Loss SNV dbSNP153 33..33 33 - - - 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 32498 RMVar_ID_32498 Human_SNP_ID_169555663 A-to-I Human chr3 - 196487041 196487041 196487041 TTTGGGGTTTTTTGTTTTTTGAGACAGGTCTTACTCTGTCATGCAGGTTGGAGTGCAGTGGCACA TTTGGGGTTTTTTGTTTTTTGAGACAGGTCTTGCTCTGTCATGCAGGTTGGAGTGCAGTGGCACA T C RNF168 Ensembl:ENSG00000163961 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909787223 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14993645 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 32499 RMVar_ID_32499 Human_SNP_ID_169559213 A-to-I Human chr3 - 196499463 196499463 196499463 ACTTCATATAAATGGAATTCTTTTTATTTCCTAGGGCTACTGTAACAAAGTACCACGAACTTAGC ACTTCATATAAATGGAATTCTTTTTATTTCCTGGGGCTACTGTAACAAAGTACCACGAACTTAGC T C RNF168 Ensembl:ENSG00000163961 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1381547636 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14763069 32500 RMVar_ID_32500 Human_SNP_ID_169559270 A-to-I Human chr3 - 196499673 196499673 196499673 GGGATTACAGGCATGCGACACCACACCCAACTAATTTTTGTATTGTTAGTAGAGATGGGGTTTTG GGGATTACAGGCATGCGACACCACACCCAACTGATTTTTGTATTGTTAGTAGAGATGGGGTTTTG T C RNF168 Ensembl:ENSG00000163961 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs944139170 Functional Loss SNV dbSNP153 33..33 33 - - - 32501 RMVar_ID_32501 Human_SNP_ID_169559271 A-to-I Human chr3 - 196499673 196499673 196499673 GGGATTACAGGCATGCGACACCACACCCAACTAATTTTTGTATTGTTAGTAGAGATGGGGTTTTG GGGATTACAGGCATGCGACACCACACCCAACTCATTTTTGTATTGTTAGTAGAGATGGGGTTTTG T G RNF168 Ensembl:ENSG00000163961 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs944139170 Functional Loss SNV dbSNP153 33..33 33 - - - 32502 RMVar_ID_32502 Human_SNP_ID_169575330 A-to-I Human chr3 - 196557287 196557287 196557287 GTCCTGCCATGGCCTCCCAAAGTGCTGGGATTATAGGCATGAGCCACTGCACCTGGCCTGAAGAG GTCCTGCCATGGCCTCCCAAAGTGCTGGGATTGTAGGCATGAGCCACTGCACCTGGCCTGAAGAG T C WDR53 Ensembl:ENSG00000185798 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs779340844 Functional Loss SNV dbSNP153 33..33 33 - - - 32503 RMVar_ID_32503 Human_SNP_ID_169603014 A-to-I Human chr3 + 196657543 196657543 196657543 CAGGGTGGCCAACATGGCAAAACTCTGCCTCTACTAAAAATACAAAATTAGCCCGGTGTGGTGGT CAGGGTGGCCAACATGGCAAAACTCTGCCTCTTCTAAAAATACAAAATTAGCCCGGTGTGGTGGT A T PIGX,NRROS Ensembl:ENSG00000163964,Ensembl:ENSG00000174004 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1560055245 Functional Loss SNV dbSNP153 33..33 33 - - - 32504 RMVar_ID_32504 Human_SNP_ID_169603305 A-to-I Human chr3 + 196658627 196658627 196658627 TTGTAGGCAACCACTGCCCTTGTATTACTGATAAACTTGTGCAAACGAATGCCATTGCTCCTCTA TTGTAGGCAACCACTGCCCTTGTATTACTGATGAACTTGTGCAAACGAATGCCATTGCTCCTCTA A G PIGX,NRROS Ensembl:ENSG00000163964,Ensembl:ENSG00000174004 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1099215 Functional Loss SNV dbSNP153 33..33 33 - - - 32505 RMVar_ID_32505 Human_SNP_ID_169603306 A-to-I Human chr3 + 196658627 196658627 196658627 TTGTAGGCAACCACTGCCCTTGTATTACTGATAAACTTGTGCAAACGAATGCCATTGCTCCTCTA TTGTAGGCAACCACTGCCCTTGTATTACTGATTAACTTGTGCAAACGAATGCCATTGCTCCTCTA A T PIGX,NRROS Ensembl:ENSG00000163964,Ensembl:ENSG00000174004 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1099215 Functional Loss SNV dbSNP153 33..33 33 - - - 32506 RMVar_ID_32506 Human_SNP_ID_169619414 A-to-I Human chr3 + 196713380 196713380 196713380 TGGAGTGCAATGGCGCGATCTCGGCTCACTGCAACCTCCGCCTTTCCCAAGTTCAAGCAATTCTT TGGAGTGCAATGGCGCGATCTCGGCTCACTGCGACCTCCGCCTTTCCCAAGTTCAAGCAATTCTT A G PIGX Ensembl:ENSG00000163964 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs570507602 Functional Loss SNV dbSNP153 33..33 33 - - - 32507 RMVar_ID_32507 Human_SNP_ID_169619757 A-to-I Human chr3 + 196714512 196714512 196714512 TTTGAGACGGAGTCTTGCTCTCTTGCCAGGCTAGTGCAGTGGCGCAATCTCGGCTTATTGCAACC TTTGAGACGGAGTCTTGCTCTCTTGCCAGGCTGGTGCAGTGGCGCAATCTCGGCTTATTGCAACC A G PIGX Ensembl:ENSG00000163964 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1464834018 Functional Loss SNV dbSNP153 33..33 33 - - - 32508 RMVar_ID_32508 Human_SNP_ID_169619805 A-to-I Human chr3 + 196714720 196714720 196714720 TTGACCTTGTGATCTGCCTGCCTCCCCCTCCCAAAGTGCTGGGATTACAGGCATGAGTCACTGCA TTGACCTTGTGATCTGCCTGCCTCCCCCTCCCGAAGTGCTGGGATTACAGGCATGAGTCACTGCA A G PIGX Ensembl:ENSG00000163964 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1289318726 Functional Loss SNV dbSNP153 33..33 33 - - - 32509 RMVar_ID_32509 Human_SNP_ID_169619806 A-to-I Human chr3 + 196714720 196714720 196714720 TTGACCTTGTGATCTGCCTGCCTCCCCCTCCCAAAGTGCTGGGATTACAGGCATGAGTCACTGCA TTGACCTTGTGATCTGCCTGCCTCCCCCTCCCTAAGTGCTGGGATTACAGGCATGAGTCACTGCA A T PIGX Ensembl:ENSG00000163964 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1289318726 Functional Loss SNV dbSNP153 33..33 33 - - - 32510 RMVar_ID_32510 Human_SNP_ID_169624847 A-to-I Human chr3 + 196734452 196734452 196734452 GGGGCTGGTGGTGGGCATCTGTAGTCCCAGCTAATTGGAAGGGTGAGGCGGGAGGATCGCTTGAA GGGGCTGGTGGTGGGCATCTGTAGTCCCAGCTGATTGGAAGGGTGAGGCGGGAGGATCGCTTGAA A G PIGX Ensembl:ENSG00000163964 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1363609771 Functional Loss SNV dbSNP153 33..33 33 - - - 32511 RMVar_ID_32511 Human_SNP_ID_169627006 A-to-I Human chr3 + 196742206 196742204 196742207 CGCCTCCTGGGTTCAAGCGATTCTCCTGTCTCAGCCTGCTGAGTAGCTGGGATTACAGGCACGCG CGCCTCCTGGGTTCAAGCGATTCTCCTGTCT___CCTGCTGAGTAGCTGGGATTACAGGCACGCG TCAG T PAK2 Ensembl:ENSG00000180370 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1201530603 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_223942,RMVar_hsa_circ_122437 32512 RMVar_ID_32512 Human_SNP_ID_169627214 A-to-I Human chr3 + 196742861 196742861 196742861 ATGGCGTGATGAACCCGGGAGGCGGAGCTTGCAGTGAGTCGAGATCGCGCCACTGCACTCCCGCC ATGGCGTGATGAACCCGGGAGGCGGAGCTTGCGGTGAGTCGAGATCGCGCCACTGCACTCCCGCC A G PAK2 Ensembl:ENSG00000180370 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1457272341 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_223942,RMVar_hsa_circ_122437 32513 RMVar_ID_32513 Human_SNP_ID_169627215 A-to-I Human chr3 + 196742861 196742861 196742861 ATGGCGTGATGAACCCGGGAGGCGGAGCTTGCAGTGAGTCGAGATCGCGCCACTGCACTCCCGCC ATGGCGTGATGAACCCGGGAGGCGGAGCTTGCTGTGAGTCGAGATCGCGCCACTGCACTCCCGCC A T PAK2 Ensembl:ENSG00000180370 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1457272341 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_223942,RMVar_hsa_circ_122437 32514 RMVar_ID_32514 Human_SNP_ID_169627838 A-to-I Human chr3 + 196745184 196745184 196745184 GTCACTCAGGCTGGAGTGCAGTGTTGGATCTCAGCTCACTGCAACTTCCGCCTCCCGGGTTCAAG GTCACTCAGGCTGGAGTGCAGTGTTGGATCTCGGCTCACTGCAACTTCCGCCTCCCGGGTTCAAG A G PAK2 Ensembl:ENSG00000180370 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1175353497 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_223942,RMVar_hsa_circ_122437 32515 RMVar_ID_32515 Human_SNP_ID_169627965 A-to-I Human chr3 + 196745622 196745621 196745622 GATCACCTGATGTCAGCAGTTGGAAACAGCCTAACCAACGTGGTGAAACCTTGTGTCTACTGAAA GATCACCTGATGTCAGCAGTTGGAAACAGCCT_ACCAACGTGGTGAAACCTTGTGTCTACTGAAA TA T PAK2 Ensembl:ENSG00000180370 Protein coding intron GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-Seq:(High) rs1485050135 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_223942,RMVar_hsa_circ_122437 32516 RMVar_ID_32516 Human_SNP_ID_169647599 A-to-I Human chr3 + 196815666 196815666 196815666 AAAATTAGCTGGGTGTGGTGGTACGCGCCTGTAGTCTCAGCTACTCGGGAGGCTGAGACGGGAGA AAAATTAGCTGGGTGTGGTGGTACGCGCCTGTGGTCTCAGCTACTCGGGAGGCTGAGACGGGAGA A G PAK2 Ensembl:ENSG00000180370 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1481228876 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25725481 RMVar_hsa_circ_10708,RMVar_hsa_circ_93347,RMVar_hsa_circ_366293,RMVar_hsa_circ_73259,RMVar_hsa_circ_278974,RMVar_hsa_circ_272228,RMVar_hsa_circ_223952,RMVar_hsa_circ_223953,RMVar_hsa_circ_223951,RMVar_hsa_circ_223955,RMVar_hsa_circ_114048,RMVar_hsa_circ_313678,RMVar_hsa_circ_293612,RMVar_hsa_circ_223956,RMVar_hsa_circ_54995,RMVar_hsa_circ_306927,RMVar_hsa_circ_39118,RMVar_hsa_circ_349862,RMVar_hsa_circ_223958,RMVar_hsa_circ_303084,RMVar_hsa_circ_223957,RMVar_hsa_circ_294669 32517 RMVar_ID_32517 Human_SNP_ID_169648547 A-to-I Human chr3 + 196819277 196819277 196819277 CAGACTGAGCAACATGGCAAGACTCCATCTCTACTAAAAATACAACAATTAGCCGGGCGTGGTGG CAGACTGAGCAACATGGCAAGACTCCATCTCTGCTAAAAATACAACAATTAGCCGGGCGTGGTGG A G PAK2 Ensembl:ENSG00000180370 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs546126647 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10708,RMVar_hsa_circ_93347,RMVar_hsa_circ_73259,RMVar_hsa_circ_278974,RMVar_hsa_circ_223952,RMVar_hsa_circ_223953,RMVar_hsa_circ_223955,RMVar_hsa_circ_114048,RMVar_hsa_circ_293612,RMVar_hsa_circ_306927,RMVar_hsa_circ_349862,RMVar_hsa_circ_303084,RMVar_hsa_circ_223957,RMVar_hsa_circ_60794,RMVar_hsa_circ_305138 32518 RMVar_ID_32518 Human_SNP_ID_169651203 A-to-I Human chr3 + 196828839 196828839 196828839 CTTTCTCTCCTTCATAGCTTTTCTTTTCCTGGACTTGCTCCTTTTGAGTTGCTTTTGCGTTTCTC CTTTCTCTCCTTCATAGCTTTTCTTTTCCTGGGCTTGCTCCTTTTGAGTTGCTTTTGCGTTTCTC A G PAK2 Ensembl:ENSG00000180370 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs759780366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7176754,Human_RBP_ID_14763715,Human_RBP_ID_17292303,Human_RBP_ID_18182024,Human_RBP_ID_24428704,Human_RBP_ID_24497362 Human_miRNA_ID_3097174 RMVar_hsa_circ_93347,RMVar_hsa_circ_223953 32519 RMVar_ID_32519 Human_SNP_ID_169662342 A-to-I Human chr3 + 196869232 196869232 196869232 ACAATTTTTTTTTGGAGGGGGGACAGGGTCTCACTCTGACACCCAGCCTGGAGTGCAGTGGCGCG ACAATTTTTTTTTGGAGGGGGGACAGGGTCTCCCTCTGACACCCAGCCTGGAGTGCAGTGGCGCG A C SENP5 Ensembl:ENSG00000119231 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903069621 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_223959,RMVar_hsa_circ_99857 32520 RMVar_ID_32520 Human_SNP_ID_169671784 A-to-I Human chr3 + 196904538 196904537 196904538 GGCCAGGTGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGCGGATCACT GGCCAGGTGCGGTGGCTCACGCCTGTAATCCC_GCACTTTGGGAGGCTGAGGTGGGCGGATCACT CA C SENP5 Ensembl:ENSG00000119231 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs547795199 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_29766,RMVar_hsa_circ_61032,RMVar_hsa_circ_223959,RMVar_hsa_circ_99857,RMVar_hsa_circ_80598,RMVar_hsa_circ_223962,RMVar_hsa_circ_76565,RMVar_hsa_circ_223966 32521 RMVar_ID_32521 Human_SNP_ID_169671932 A-to-I Human chr3 + 196905083 196905083 196905083 CACCGTACCCGGCTAATTCTTGTATTTTTAATAGAGACGGGATTTCACTATGTTGGCCAGGCTGG CACCGTACCCGGCTAATTCTTGTATTTTTAATTGAGACGGGATTTCACTATGTTGGCCAGGCTGG A T SENP5 Ensembl:ENSG00000119231 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1293057443 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29766,RMVar_hsa_circ_61032,RMVar_hsa_circ_223959,RMVar_hsa_circ_99857,RMVar_hsa_circ_80598,RMVar_hsa_circ_223962,RMVar_hsa_circ_76565,RMVar_hsa_circ_223966 32522 RMVar_ID_32522 Human_SNP_ID_169673363 A-to-I Human chr3 + 196910620 196910620 196910620 CGCCTGCCTCGGCCTTCCAGAGTGCTGGGATTATAGATGTGAGCCACCACTCCTGGCTGCCCAAA CGCCTGCCTCGGCCTTCCAGAGTGCTGGGATTGTAGATGTGAGCCACCACTCCTGGCTGCCCAAA A G SENP5 Ensembl:ENSG00000119231 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1030309296 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29766,RMVar_hsa_circ_61032,RMVar_hsa_circ_223959,RMVar_hsa_circ_99857,RMVar_hsa_circ_80598,RMVar_hsa_circ_223962,RMVar_hsa_circ_76565,RMVar_hsa_circ_223966 32523 RMVar_ID_32523 Human_SNP_ID_169673557 A-to-I Human chr3 + 196911437 196911437 196911437 GACACTTCGCAAAAGAAGACATTTATGTCTGTAGTCTCAGCTACTCGAGAGGCTGAGACAGGAGA GACACTTCGCAAAAGAAGACATTTATGTCTGTCGTCTCAGCTACTCGAGAGGCTGAGACAGGAGA A C SENP5 Ensembl:ENSG00000119231 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1043115866 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19029119 RMVar_hsa_circ_29766,RMVar_hsa_circ_61032,RMVar_hsa_circ_223959,RMVar_hsa_circ_99857,RMVar_hsa_circ_80598,RMVar_hsa_circ_223962,RMVar_hsa_circ_76565,RMVar_hsa_circ_223966 32524 RMVar_ID_32524 Human_SNP_ID_169673663 A-to-I Human chr3 + 196911742 196911742 196911742 TGAGGCAGGAGAATCGCTTGAACCTGAGAGGCAGAGGTTGCGTGAGCTGAGATTGTGCCATTGCA TGAGGCAGGAGAATCGCTTGAACCTGAGAGGCGGAGGTTGCGTGAGCTGAGATTGTGCCATTGCA A G SENP5 Ensembl:ENSG00000119231 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388629737 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29766,RMVar_hsa_circ_61032,RMVar_hsa_circ_223959,RMVar_hsa_circ_99857,RMVar_hsa_circ_80598,RMVar_hsa_circ_223962,RMVar_hsa_circ_76565,RMVar_hsa_circ_223966 32525 RMVar_ID_32525 Human_SNP_ID_169674091 A-to-I Human chr3 + 196913449 196913449 196913449 AAAATTAGCTGGGTGTGGTGGTGTGCGCCTGTAATCCCAGCTATTCGGGAGGCTGAGGCAGAGAA AAAATTAGCTGGGTGTGGTGGTGTGCGCCTGTGATCCCAGCTATTCGGGAGGCTGAGGCAGAGAA A G AC016949.1,SENP5 Ensembl:ENSG00000230732,Ensembl:ENSG00000119231 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs943086088 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29766,RMVar_hsa_circ_61032,RMVar_hsa_circ_223959,RMVar_hsa_circ_99857,RMVar_hsa_circ_80598,RMVar_hsa_circ_223962,RMVar_hsa_circ_76565,RMVar_hsa_circ_223966 32526 RMVar_ID_32526 Human_SNP_ID_169675121 A-to-I Human chr3 + 196916710 196916710 196916710 CCACTATGCCTGGCTAATTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGATGGTCGGACTGG CCACTATGCCTGGCTAATTTTGTATTTTTAGTGGAGACAGGGTTTCACCATGATGGTCGGACTGG A G SENP5 Ensembl:ENSG00000119231 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1051057755 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29766,RMVar_hsa_circ_61032,RMVar_hsa_circ_223959,RMVar_hsa_circ_99857,RMVar_hsa_circ_80598,RMVar_hsa_circ_223962,RMVar_hsa_circ_76565,RMVar_hsa_circ_223966 32527 RMVar_ID_32527 Human_SNP_ID_169675126 A-to-I Human chr3 + 196916724 196916724 196916724 TAATTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGATGGTCGGACTGGTCTCAAACTCCTGA TAATTTTGTATTTTTAGTAGAGACAGGGTTTCCCCATGATGGTCGGACTGGTCTCAAACTCCTGA A C SENP5 Ensembl:ENSG00000119231 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs535992580 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29766,RMVar_hsa_circ_61032,RMVar_hsa_circ_223959,RMVar_hsa_circ_99857,RMVar_hsa_circ_80598,RMVar_hsa_circ_223962,RMVar_hsa_circ_76565,RMVar_hsa_circ_223966 32528 RMVar_ID_32528 Human_SNP_ID_169675128 A-to-I Human chr3 + 196916727 196916727 196916727 TTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGATGGTCGGACTGGTCTCAAACTCCTGACCT TTTTGTATTTTTAGTAGAGACAGGGTTTCACCGTGATGGTCGGACTGGTCTCAAACTCCTGACCT A G SENP5 Ensembl:ENSG00000119231 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1451971868 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29766,RMVar_hsa_circ_61032,RMVar_hsa_circ_223959,RMVar_hsa_circ_99857,RMVar_hsa_circ_80598,RMVar_hsa_circ_223962,RMVar_hsa_circ_76565,RMVar_hsa_circ_223966 32529 RMVar_ID_32529 Human_SNP_ID_169675218 A-to-I Human chr3 + 196917036 196917036 196917036 CAGGTCTGTAATCCCAGGTATGCAGAACGCTGAAGCACAAGAATCGCTTGAACCTGGGAGACAGA CAGGTCTGTAATCCCAGGTATGCAGAACGCTGGAGCACAAGAATCGCTTGAACCTGGGAGACAGA A G SENP5 Ensembl:ENSG00000119231 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs78849968 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29766,RMVar_hsa_circ_61032,RMVar_hsa_circ_223959,RMVar_hsa_circ_99857,RMVar_hsa_circ_80598,RMVar_hsa_circ_223962,RMVar_hsa_circ_76565,RMVar_hsa_circ_223966 32530 RMVar_ID_32530 Human_SNP_ID_169676695 A-to-I Human chr3 + 196922812 196922812 196922812 CCCGGTTAGTTTTTGTATTTTTTTGTAGATACAGTGTTTCGCCATGTCACCCAGGCTGGTCCTGA CCCGGTTAGTTTTTGTATTTTTTTGTAGATACGGTGTTTCGCCATGTCACCCAGGCTGGTCCTGA A G SENP5 Ensembl:ENSG00000119231 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900897284 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14764108 RMVar_hsa_circ_29766,RMVar_hsa_circ_61032,RMVar_hsa_circ_223959,RMVar_hsa_circ_99857,RMVar_hsa_circ_80598,RMVar_hsa_circ_223962,RMVar_hsa_circ_76565,RMVar_hsa_circ_223966 32531 RMVar_ID_32531 Human_SNP_ID_169681109 A-to-I Human chr3 - 196940108 196940108 196940108 CACTCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCGCCTGACCCCGATGA CACTCGCCTCAGCCTCCCAAAGTGCTGGGATTGCAGGCATGAGCCACCGCGCCTGACCCCGATGA T C NCBP2 Ensembl:ENSG00000114503 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs970031674 Functional Loss SNV dbSNP153 33..33 33 - - - 32532 RMVar_ID_32532 Human_SNP_ID_169681110 A-to-I Human chr3 - 196940108 196940108 196940108 CACTCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCGCCTGACCCCGATGA CACTCGCCTCAGCCTCCCAAAGTGCTGGGATTCCAGGCATGAGCCACCGCGCCTGACCCCGATGA T G NCBP2 Ensembl:ENSG00000114503 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs970031674 Functional Loss SNV dbSNP153 33..33 33 - - - 32533 RMVar_ID_32533 Human_SNP_ID_169681113 A-to-I Human chr3 - 196940121 196940121 196940121 ACCTCAGGCGATCCACTCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCGC ACCTCAGGCGATCCACTCGCCTCAGCCTCCCAGAGTGCTGGGATTACAGGCATGAGCCACCGCGC T C NCBP2 Ensembl:ENSG00000114503 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs757997496 Functional Loss SNV dbSNP153 33..33 33 - - - 32534 RMVar_ID_32534 Human_SNP_ID_169681132 A-to-I Human chr3 - 196940177 196940177 196940177 TTTAGTAGAGACAGGGTTTCATTCACTATGTTAGCCAGGCTGGTCTCAAACTCTTGACCTCAGGC TTTAGTAGAGACAGGGTTTCATTCACTATGTTGGCCAGGCTGGTCTCAAACTCTTGACCTCAGGC T C NCBP2 Ensembl:ENSG00000114503 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1284511587 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14764661 32535 RMVar_ID_32535 Human_SNP_ID_169693747 A-to-I Human chr3 + 196981095 196981095 196981095 CTCAGGTCTGCACAAAAGCCTTATATGAGGCCAGGCGTGGTGGCTCACGCCTGTAATCCCAGCAC CTCAGGTCTGCACAAAAGCCTTATATGAGGCCGGGCGTGGTGGCTCACGCCTGTAATCCCAGCAC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs543236238 Functional Loss SNV dbSNP153 33..33 33 - - - 32536 RMVar_ID_32536 Human_SNP_ID_169704509 A-to-I Human chr3 - 197017871 197017871 197017871 TCTCACCCAAAGCCTTTCTTTTTTTTTGAGACAGAGTTTCGCTCTGTCGCCCAGGCTGGAGTGCA TCTCACCCAAAGCCTTTCTTTTTTTTTGAGACGGAGTTTCGCTCTGTCGCCCAGGCTGGAGTGCA T C MELTF Ensembl:ENSG00000163975 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1267045896 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_158472 RMVar_hsa_circ_18293 32537 RMVar_ID_32537 Human_SNP_ID_169704765 A-to-I Human chr3 - 197018579 197018579 197018579 AGCCAGGCATCTTGGTGCACACCTGTAATCTGAGCTACTCGGGAGGCTGAGGCAGAAGAATAACT AGCCAGGCATCTTGGTGCACACCTGTAATCTGTGCTACTCGGGAGGCTGAGGCAGAAGAATAACT T A MELTF Ensembl:ENSG00000163975 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs142071930 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18293 32538 RMVar_ID_32538 Human_SNP_ID_169704802 A-to-I Human chr3 - 197018687 197018687 197018687 TAATCCCAGCACTTTGGGAGGCCGAGGCTGGCAGATCATGAGGTCAGGGGTTCAAGACCGGCCTG TAATCCCAGCACTTTGGGAGGCCGAGGCTGGCGGATCATGAGGTCAGGGGTTCAAGACCGGCCTG T C MELTF Ensembl:ENSG00000163975 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1323761407 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18293 32539 RMVar_ID_32539 Human_SNP_ID_169704815 A-to-I Human chr3 - 197018717 197018717 197018717 AAGGAGGCTGGGCACGGTGCCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCTGGCAGA AAGGAGGCTGGGCACGGTGCCTCACGCCTGTAGTCCCAGCACTTTGGGAGGCCGAGGCTGGCAGA T C MELTF Ensembl:ENSG00000163975 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs921517578 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18293 32540 RMVar_ID_32540 Human_SNP_ID_169715323 A-to-I Human chr3 - 197052113 197052113 197052113 AAACAGGCTGGGCTCGGTGGCTCACATCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGAGCAGA AAACAGGCTGGGCTCGGTGGCTCACATCTGTATTCCCAGCACTTTGGGAGGCCAAGGCGAGCAGA T A DLG1 Ensembl:ENSG00000075711 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264521274 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85652,RMVar_hsa_circ_278366,RMVar_hsa_circ_311911,RMVar_hsa_circ_320958,RMVar_hsa_circ_297506,RMVar_hsa_circ_272120,RMVar_hsa_circ_223975,RMVar_hsa_circ_17343,RMVar_hsa_circ_28485,RMVar_hsa_circ_223977,RMVar_hsa_circ_223978,RMVar_hsa_circ_223976,RMVar_hsa_circ_223973,RMVar_hsa_circ_223974 32541 RMVar_ID_32541 Human_SNP_ID_169726152 A-to-I Human chr3 - 197093299 197093299 197093299 CAAAAATTAGCTGGGCATGTTAGCGCATGTCTATAGTCCCAGCTCCTTGGGAGGCTGAAGCAGGA CAAAAATTAGCTGGGCATGTTAGCGCATGTCTGTAGTCCCAGCTCCTTGGGAGGCTGAAGCAGGA T C DLG1 Ensembl:ENSG00000075711 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs575717765 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5763,RMVar_hsa_circ_85652,RMVar_hsa_circ_297506,RMVar_hsa_circ_223981,RMVar_hsa_circ_223973,RMVar_hsa_circ_223974,RMVar_hsa_circ_310965,RMVar_hsa_circ_341386,RMVar_hsa_circ_223982,RMVar_hsa_circ_93038,RMVar_hsa_circ_3357,RMVar_hsa_circ_223984,RMVar_hsa_circ_333126,RMVar_hsa_circ_294112,RMVar_hsa_circ_376756,RMVar_hsa_circ_223985,RMVar_hsa_circ_326025,RMVar_hsa_circ_267147,RMVar_hsa_circ_53949,RMVar_hsa_circ_71965,RMVar_hsa_circ_223986,RMVar_hsa_circ_221,RMVar_hsa_circ_320592,RMVar_hsa_circ_290538,RMVar_hsa_circ_322818,RMVar_hsa_circ_273633,RMVar_hsa_circ_223989,RMVar_hsa_circ_29084,RMVar_hsa_circ_223990,RMVar_hsa_circ_286389,RMVar_hsa_circ_288731,RMVar_hsa_circ_279367,RMVar_hsa_circ_223996,RMVar_hsa_circ_53827,RMVar_hsa_circ_223992,RMVar_hsa_circ_223993,RMVar_hsa_circ_303869,RMVar_hsa_circ_341360,RMVar_hsa_circ_223991,RMVar_hsa_circ_311760,RMVar_hsa_circ_270761,RMVar_hsa_circ_24766,RMVar_hsa_circ_38198,RMVar_hsa_circ_223998,RMVar_hsa_circ_223999,RMVar_hsa_circ_223997 32542 RMVar_ID_32542 Human_SNP_ID_169732764 A-to-I Human chr3 - 197119755 197119755 197119755 AAGTAATCTGGGTGTGGTGGCTTATGCCTGTAATCCCAACACTTTGGGAGGCTGAGGTGGGAGTA AAGTAATCTGGGTGTGGTGGCTTATGCCTGTATTCCCAACACTTTGGGAGGCTGAGGTGGGAGTA T A DLG1 Ensembl:ENSG00000075711 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs891363227 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14765713 RMVar_hsa_circ_5763,RMVar_hsa_circ_85652,RMVar_hsa_circ_223973,RMVar_hsa_circ_36974,RMVar_hsa_circ_376756,RMVar_hsa_circ_267147,RMVar_hsa_circ_53949,RMVar_hsa_circ_71965,RMVar_hsa_circ_29084,RMVar_hsa_circ_303869,RMVar_hsa_circ_341360,RMVar_hsa_circ_311760,RMVar_hsa_circ_24766,RMVar_hsa_circ_223998,RMVar_hsa_circ_223999,RMVar_hsa_circ_223997,RMVar_hsa_circ_224000,RMVar_hsa_circ_325363,RMVar_hsa_circ_367874,RMVar_hsa_circ_325633,RMVar_hsa_circ_292693,RMVar_hsa_circ_291698,RMVar_hsa_circ_224002,RMVar_hsa_circ_224003,RMVar_hsa_circ_224001,RMVar_hsa_circ_333267,RMVar_hsa_circ_334425,RMVar_hsa_circ_348767,RMVar_hsa_circ_287474,RMVar_hsa_circ_91286,RMVar_hsa_circ_120559,RMVar_hsa_circ_45339,RMVar_hsa_circ_224013,RMVar_hsa_circ_224006,RMVar_hsa_circ_224008,RMVar_hsa_circ_224010,RMVar_hsa_circ_224011,RMVar_hsa_circ_224009,RMVar_hsa_circ_224007,RMVar_hsa_circ_310058,RMVar_hsa_circ_345164,RMVar_hsa_circ_278878,RMVar_hsa_circ_60309,RMVar_hsa_circ_90720,RMVar_hsa_circ_224015,RMVar_hsa_circ_53746,RMVar_hsa_circ_224014 32543 RMVar_ID_32543 Human_SNP_ID_169770277 A-to-I Human chr3 - 197267427 197267427 197267427 GAACATATTATATTTACAAGATAAAGTGAAGAAGGGAACAGAGGCCCAAGATGGAAAAAGAGATT GAACATATTATATTTACAAGATAAAGTGAAGAGGGGAACAGAGGCCCAAGATGGAAAAAGAGATT T C DLG1 Ensembl:ENSG00000075711 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1260425378 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71965,RMVar_hsa_circ_91286,RMVar_hsa_circ_120559,RMVar_hsa_circ_224010,RMVar_hsa_circ_224011,RMVar_hsa_circ_90720,RMVar_hsa_circ_224015,RMVar_hsa_circ_59660,RMVar_hsa_circ_118081,RMVar_hsa_circ_224024,RMVar_hsa_circ_331101,RMVar_hsa_circ_109228,RMVar_hsa_circ_224029 32544 RMVar_ID_32544 Human_SNP_ID_169772305 A-to-I Human chr3 - 197274927 197274927 197274927 GCCTGCCTCGGCCTCCCATGTGCTGGGATTACAGGCGTGAGCCACCGTGCCCAGCTTATTATGGT GCCTGCCTCGGCCTCCCATGTGCTGGGATTACGGGCGTGAGCCACCGTGCCCAGCTTATTATGGT T C DLG1 Ensembl:ENSG00000075711 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs981659061 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71965,RMVar_hsa_circ_91286,RMVar_hsa_circ_120559,RMVar_hsa_circ_224010,RMVar_hsa_circ_224011,RMVar_hsa_circ_90720,RMVar_hsa_circ_224015,RMVar_hsa_circ_59660,RMVar_hsa_circ_118081,RMVar_hsa_circ_224024,RMVar_hsa_circ_331101,RMVar_hsa_circ_109228,RMVar_hsa_circ_224030,RMVar_hsa_circ_224029 32545 RMVar_ID_32545 Human_SNP_ID_169772551 A-to-I Human chr3 - 197275797 197275797 197275797 TATAGTCACCTACTGTGCTATTGAACACTTCTAATTGTATTTTTGTACCCATTAACCAACTTGTC TATAGTCACCTACTGTGCTATTGAACACTTCTTATTGTATTTTTGTACCCATTAACCAACTTGTC T A DLG1 Ensembl:ENSG00000075711 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223695477 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3702320 RMVar_hsa_circ_71965,RMVar_hsa_circ_91286,RMVar_hsa_circ_120559,RMVar_hsa_circ_224010,RMVar_hsa_circ_224011,RMVar_hsa_circ_90720,RMVar_hsa_circ_224015,RMVar_hsa_circ_59660,RMVar_hsa_circ_118081,RMVar_hsa_circ_224024,RMVar_hsa_circ_331101,RMVar_hsa_circ_109228,RMVar_hsa_circ_224030,RMVar_hsa_circ_224029 32546 RMVar_ID_32546 Human_SNP_ID_169773156 A-to-I Human chr3 - 197278159 197278159 197278159 TCCACCTCAGCCTCCCGAGTAGCTGGGATTACAGCACCCACCATCATACACGGCTAATTTTTGTA TCCACCTCAGCCTCCCGAGTAGCTGGGATTACGGCACCCACCATCATACACGGCTAATTTTTGTA T C DLG1 Ensembl:ENSG00000075711 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1408879417 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71965,RMVar_hsa_circ_91286,RMVar_hsa_circ_120559,RMVar_hsa_circ_224010,RMVar_hsa_circ_224011,RMVar_hsa_circ_90720,RMVar_hsa_circ_224015,RMVar_hsa_circ_59660,RMVar_hsa_circ_118081,RMVar_hsa_circ_224024,RMVar_hsa_circ_331101,RMVar_hsa_circ_109228,RMVar_hsa_circ_224030,RMVar_hsa_circ_224029 32547 RMVar_ID_32547 Human_SNP_ID_169843733 A-to-I Human chr3 - 197535810 197535810 197535810 GAACTCCTGAGCTCAAGCAATCTGCCCACCTCAGCCTCCCAAAGCGCTGGGATTACAGGCATGAG GAACTCCTGAGCTCAAGCAATCTGCCCACCTCGGCCTCCCAAAGCGCTGGGATTACAGGCATGAG T C BDH1 Ensembl:ENSG00000161267 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs529882630 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_224033,RMVar_hsa_circ_350769,RMVar_hsa_circ_361922 32548 RMVar_ID_32548 Human_SNP_ID_169843758 A-to-I Human chr3 - 197535897 197535897 197535897 GGACTTAAAGGCGTGAGCCACCACACCTGACTAATTTTCGTATTTTTTGTAGAGATGGGGTTTCG GGACTTAAAGGCGTGAGCCACCACACCTGACTCATTTTCGTATTTTTTGTAGAGATGGGGTTTCG T G BDH1 Ensembl:ENSG00000161267 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1428101262 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_224033,RMVar_hsa_circ_350769,RMVar_hsa_circ_361922 32549 RMVar_ID_32549 Human_SNP_ID_169843906 A-to-I Human chr3 - 197536578 197536578 197536578 CCTCGGCCTCCCAAAGTGCTGGGGTTACAGGGATGACCCACCATGCCCGGCCGCATGTATGGTTT CCTCGGCCTCCCAAAGTGCTGGGGTTACAGGGTTGACCCACCATGCCCGGCCGCATGTATGGTTT T A BDH1 Ensembl:ENSG00000161267 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs752373831 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17573971 RMVar_hsa_circ_224033,RMVar_hsa_circ_350769,RMVar_hsa_circ_361922 32550 RMVar_ID_32550 Human_SNP_ID_169843927 A-to-I Human chr3 - 197536661 197536661 197536661 GTTTTTTGTATTTTTAGTAGAGTCAGGGTTTCACCATGTCGGCCAGGCTGGTCTTGAACTCCTGA GTTTTTTGTATTTTTAGTAGAGTCAGGGTTTCTCCATGTCGGCCAGGCTGGTCTTGAACTCCTGA T A BDH1 Ensembl:ENSG00000161267 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs569254863 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_224033,RMVar_hsa_circ_350769,RMVar_hsa_circ_361922 32551 RMVar_ID_32551 Human_SNP_ID_169844040 A-to-I Human chr3 - 197537096 197537096 197537096 TAGTCCCAGCTACTGGGGAGGCTGAGGTGGAAAGATTGCTTGAGTGTGGCAGGCGGAGGCTGCAG TAGTCCCAGCTACTGGGGAGGCTGAGGTGGAAGGATTGCTTGAGTGTGGCAGGCGGAGGCTGCAG T C BDH1 Ensembl:ENSG00000161267 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs981151557 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22481014 RMVar_hsa_circ_224033,RMVar_hsa_circ_350769,RMVar_hsa_circ_361922 32552 RMVar_ID_32552 Human_SNP_ID_169844044 A-to-I Human chr3 - 197537117 197537117 197537117 GAACCTGGTGGTGCATGCCTGTAGTCCCAGCTACTGGGGAGGCTGAGGTGGAAAGATTGCTTGAG GAACCTGGTGGTGCATGCCTGTAGTCCCAGCTTCTGGGGAGGCTGAGGTGGAAAGATTGCTTGAG T A BDH1 Ensembl:ENSG00000161267 Protein coding intron GSE38233;GSE100210;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,cerebellum - 24183664,29129909,30559470 RNA-Seq:(High) rs770131735 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22481014 RMVar_hsa_circ_224033,RMVar_hsa_circ_350769,RMVar_hsa_circ_361922 32553 RMVar_ID_32553 Human_SNP_ID_169844355 A-to-I Human chr3 - 197538589 197538589 197538589 CCAGTACTTTGGGAGGCCGAGGCAGGCGGATCACCTGAGGTCAGGAGTTCGAGACCAGTGTGGCC CCAGTACTTTGGGAGGCCGAGGCAGGCGGATCTCCTGAGGTCAGGAGTTCGAGACCAGTGTGGCC T A BDH1 Ensembl:ENSG00000161267 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1389463259 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_224033,RMVar_hsa_circ_350769,RMVar_hsa_circ_361922 32554 RMVar_ID_32554 Human_SNP_ID_169844693 A-to-I Human chr3 - 197540188 197540185 197540189 TTAGCAGGGCGTGGTGGAACATGCCTATAATAATCCCAGCTACTTGGGAGCCAGAGGCACGAGAA TTAGCAGGGCGTGGTGGAACATGCCTATAAT____CCAGCTACTTGGGAGCCAGAGGCACGAGAA GGATT G BDH1 Ensembl:ENSG00000161267 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1253381596 Functional Loss DEL dbSNP153 32..35 33 - - - RMVar_hsa_circ_224033,RMVar_hsa_circ_350769,RMVar_hsa_circ_361922 32555 RMVar_ID_32555 Human_SNP_ID_169850446 A-to-I Human chr3 - 197564015 197564015 197564015 TCACTGCAACCTCCGCTTCCTGGGTTCAAGCAATTCTCCTGCCTCAGCTTTCCAAGTAGCTGTGA TCACTGCAACCTCCGCTTCCTGGGTTCAAGCAGTTCTCCTGCCTCAGCTTTCCAAGTAGCTGTGA T C BDH1 Ensembl:ENSG00000161267 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs890066972 Functional Loss SNV dbSNP153 33..33 33 - - - 32556 RMVar_ID_32556 Human_SNP_ID_169850447 A-to-I Human chr3 - 197564019 197564019 197564019 CAGCTCACTGCAACCTCCGCTTCCTGGGTTCAAGCAATTCTCCTGCCTCAGCTTTCCAAGTAGCT CAGCTCACTGCAACCTCCGCTTCCTGGGTTCAGGCAATTCTCCTGCCTCAGCTTTCCAAGTAGCT T C BDH1 Ensembl:ENSG00000161267 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1307628749 Functional Loss SNV dbSNP153 33..33 33 - - - 32557 RMVar_ID_32557 Human_SNP_ID_169863448 A-to-I Human chr3 - 197609190 197609190 197609190 AAATTAGCCAGGTGTGGTGGTGGGCGCCTGCAATCTCAGCTACTCGGGAGTCTGAGGCAGGAGAA AAATTAGCCAGGTGTGGTGGTGGGCGCCTGCAGTCTCAGCTACTCGGGAGTCTGAGGCAGGAGAA T C AC132008.2 Ensembl:ENSG00000214135 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1397533614 Functional Loss SNV dbSNP153 33..33 33 - - - 32558 RMVar_ID_32558 Human_SNP_ID_169864394 A-to-I Human chr3 - 197612712 197612712 197612712 ATCGCTTGAGCCTAGGTGTTTGACACCAGCCTAGACAACATTGTGAGACTCTGTCTCAAAAATAA ATCGCTTGAGCCTAGGTGTTTGACACCAGCCTGGACAACATTGTGAGACTCTGTCTCAAAAATAA T C AC132008.2 Ensembl:ENSG00000214135 Pseudogene intron GSE100210;GSE112787 HepG2 cell line;293 Flip-In T-REx cells,empty vector - 29129909,29967493 RNA-Seq:(High) rs1071661 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2775658,Human_RBP_ID_3723308,Human_RBP_ID_5250080,Human_RBP_ID_7178541,Human_RBP_ID_17574508,Human_RBP_ID_17586914,Human_RBP_ID_22509347 32559 RMVar_ID_32559 Human_SNP_ID_169864408 A-to-I Human chr3 - 197612762 197612762 197612762 TGGTGGTACATGCCTGTAGTCCCAGCTACTCAAGAGGATGGGGCCAGAGGATCGCTTGAGCCTAG TGGTGGTACATGCCTGTAGTCCCAGCTACTCAGGAGGATGGGGCCAGAGGATCGCTTGAGCCTAG T C AC132008.2 Ensembl:ENSG00000214135 Pseudogene intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229,31158229 RNA-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 32560 RMVar_ID_32560 Human_SNP_ID_169864412 A-to-I Human chr3 - 197612785 197612785 197612785 TAAAATATACAAATGGTGTGGTATGGTGGTACATGCCTGTAGTCCCAGCTACTCAAGAGGATGGG TAAAATATACAAATGGTGTGGTATGGTGGTACGTGCCTGTAGTCCCAGCTACTCAAGAGGATGGG T C AC132008.2 Ensembl:ENSG00000214135 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs931097731 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2775659,Human_RBP_ID_5089816,Human_RBP_ID_17573973,Human_RBP_ID_17673807,Human_RBP_ID_18536356,Human_RBP_ID_27050519 32561 RMVar_ID_32561 Human_SNP_ID_169864413 A-to-I Human chr3 - 197612787 197612787 197612787 TTTAAAATATACAAATGGTGTGGTATGGTGGTACATGCCTGTAGTCCCAGCTACTCAAGAGGATG TTTAAAATATACAAATGGTGTGGTATGGTGGTGCATGCCTGTAGTCCCAGCTACTCAAGAGGATG T C AC132008.2 Ensembl:ENSG00000214135 Pseudogene intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs1443028249 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2775659,Human_RBP_ID_17573973,Human_RBP_ID_17673807,Human_RBP_ID_18536356,Human_RBP_ID_27050519 32562 RMVar_ID_32562 Human_SNP_ID_169864482 A-to-I Human chr3 - 197613020 197613020 197613020 GGTTCAAGTGATTCTGTTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCATGCACCACTCTTT GGTTCAAGTGATTCTGTTGCCTCAGCCTCCTGCGTAGCTGGGATTACAGGCATGCACCACTCTTT T G AC132008.2 Ensembl:ENSG00000214135 Pseudogene intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1483178531 Functional Loss SNV dbSNP153 33..33 33 - - - 32563 RMVar_ID_32563 Human_SNP_ID_169864490 A-to-I Human chr3 - 197613046 197613046 197613046 TGATCTTGGCTCACCACAACCTGCTGGGTTCAAGTGATTCTGTTGCCTCAGCCTCCTGAGTAGCT TGATCTTGGCTCACCACAACCTGCTGGGTTCAGGTGATTCTGTTGCCTCAGCCTCCTGAGTAGCT T C AC132008.2 Ensembl:ENSG00000214135 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1132062 Functional Loss SNV dbSNP153 33..33 33 - - - 32564 RMVar_ID_32564 Human_SNP_ID_169872451 A-to-I Human chr3 - 197639382 197639382 197639382 CTGATGTTCTAGATTGAGCGTCGTGCAGCTGAAGACTTGGGGAGGAGCTGATGTTGTTCGTTTTG CTGATGTTCTAGATTGAGCGTCGTGCAGCTGATGACTTGGGGAGGAGCTGATGTTGTTCGTTTTG T A lnc-RUBCN-2-001,lnc-RUBCN-2-001:2 RNACentral:URS00008BB7A3,RNACentral:URS00008C0E9B lincRNA,lincRNA exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256478464 Functional Loss SNV dbSNP153 33..33 33 - - - 32565 RMVar_ID_32565 Human_SNP_ID_169872452 A-to-I Human chr3 - 197639382 197639382 197639382 CTGATGTTCTAGATTGAGCGTCGTGCAGCTGAAGACTTGGGGAGGAGCTGATGTTGTTCGTTTTG CTGATGTTCTAGATTGAGCGTCGTGCAGCTGAGGACTTGGGGAGGAGCTGATGTTGTTCGTTTTG T C lnc-RUBCN-2-001,lnc-RUBCN-2-001:2 RNACentral:URS00008BB7A3,RNACentral:URS00008C0E9B lincRNA,lincRNA exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256478464 Functional Loss SNV dbSNP153 33..33 33 - - - 32566 RMVar_ID_32566 Human_SNP_ID_169888922 A-to-I Human chr3 - 197690316 197690316 197690316 CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCAGCTGCCACCACACCTGGCTAATTTTT CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTGCAGGCAGCTGCCACCACACCTGGCTAATTTTT T C RUBCN Ensembl:ENSG00000145016 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1407685665 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10295,RMVar_hsa_circ_33524,RMVar_hsa_circ_119802,RMVar_hsa_circ_224041,RMVar_hsa_circ_17494,RMVar_hsa_circ_91395,RMVar_hsa_circ_224042 32567 RMVar_ID_32567 Human_SNP_ID_169901222 A-to-I Human chr3 - 197735646 197735646 197735646 TCGAGGCTGCATTGAGCCGAGATCGCACCACTACACTCCAGCCTGGGTGACAGAGGAAGACCCTG TCGAGGCTGCATTGAGCCGAGATCGCACCACTGCACTCCAGCCTGGGTGACAGAGGAAGACCCTG T C RUBCN Ensembl:ENSG00000145016 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1314196870 Functional Loss SNV dbSNP153 33..33 33 - - - 32568 RMVar_ID_32568 Human_SNP_ID_169909654 A-to-I Human chr3 + 197765018 197765018 197765018 ATTACAGGTGTGCACCACCACGCCTGGTGGCTAATTTTTATATTTTTAGTAGAGACGAGGTTTCA ATTACAGGTGTGCACCACCACGCCTGGTGGCTGATTTTTATATTTTTAGTAGAGACGAGGTTTCA A G FYTTD1 Ensembl:ENSG00000122068 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1333551703 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41580,RMVar_hsa_circ_100080,RMVar_hsa_circ_280766,RMVar_hsa_circ_345105,RMVar_hsa_circ_224045,RMVar_hsa_circ_309963,RMVar_hsa_circ_44272,RMVar_hsa_circ_224047,RMVar_hsa_circ_224048,RMVar_hsa_circ_224050,RMVar_hsa_circ_323468,RMVar_hsa_circ_304869,RMVar_hsa_circ_224049 32569 RMVar_ID_32569 Human_SNP_ID_169911970 A-to-I Human chr3 + 197772861 197772861 197772861 AAACTCCTGACCTCAAGTGATCCACTCACCTCAACCTCCCAAAGTGCTGGGATTACAGGTGTGAG AAACTCCTGACCTCAAGTGATCCACTCACCTCTACCTCCCAAAGTGCTGGGATTACAGGTGTGAG A T FYTTD1 Ensembl:ENSG00000122068 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs990479652 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41580,RMVar_hsa_circ_100080,RMVar_hsa_circ_345105,RMVar_hsa_circ_224045,RMVar_hsa_circ_44272,RMVar_hsa_circ_224048 32570 RMVar_ID_32570 Human_SNP_ID_169915711 A-to-I Human chr3 + 197786842 197786842 197786842 GACGGAATACTCTGTCACCCAGGCTGCAGTGCAGTGGCACAATCTCGGCTCACTGCAGCCTCTGC GACGGAATACTCTGTCACCCAGGCTGCAGTGCGGTGGCACAATCTCGGCTCACTGCAGCCTCTGC A G FYTTD1 Ensembl:ENSG00000122068 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs553169583 Functional Loss SNV dbSNP153 33..33 33 - - - 32571 RMVar_ID_32571 Human_SNP_ID_169918091 A-to-I Human chr3 + 197794747 197794747 197794747 GTTAATCTGGCTGGGCCTGGTGGCTCTCGCCTATAATCCCAGCACTTTGGGAGGCCAGGGCGGGC GTTAATCTGGCTGGGCCTGGTGGCTCTCGCCTGTAATCCCAGCACTTTGGGAGGCCAGGGCGGGC A G LRCH3 Ensembl:ENSG00000186001 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1241069846 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268217 32572 RMVar_ID_32572 Human_SNP_ID_169921006 A-to-I Human chr3 + 197806336 197806336 197806336 TTAGTAGAGACAGGGATCTTACTGTGTTGCCCAGGCTGGTCTCAAACTCCTGAGCTCAAATGATC TTAGTAGAGACAGGGATCTTACTGTGTTGCCCCGGCTGGTCTCAAACTCCTGAGCTCAAATGATC A C LRCH3 Ensembl:ENSG00000186001 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1423492827 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_224053,RMVar_hsa_circ_268217,RMVar_hsa_circ_224054 32573 RMVar_ID_32573 Human_SNP_ID_169921692 A-to-I Human chr3 + 197809230 197809230 197809230 TGGGGTGGGAGGATCTCTCGAGCCCAAGAGGTAGAGGTTGCAGTGAGCCATGATTGTGCCACTGC TGGGGTGGGAGGATCTCTCGAGCCCAAGAGGTGGAGGTTGCAGTGAGCCATGATTGTGCCACTGC A G LRCH3 Ensembl:ENSG00000186001 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1261234927 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_224053,RMVar_hsa_circ_268217,RMVar_hsa_circ_224054 32574 RMVar_ID_32574 Human_SNP_ID_169924251 A-to-I Human chr3 + 197818944 197818944 197818944 GGTCAGGAGTTCGAGACCAGCCTGACCAACATAGTGAAACCCCATCTCTGCTAAAAATACAAAAA GGTCAGGAGTTCGAGACCAGCCTGACCAACATGGTGAAACCCCATCTCTGCTAAAAATACAAAAA A G LRCH3 Ensembl:ENSG00000186001 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1481951459 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_53166,RMVar_hsa_circ_224053,RMVar_hsa_circ_268217,RMVar_hsa_circ_294903,RMVar_hsa_circ_316087,RMVar_hsa_circ_340719,RMVar_hsa_circ_362064,RMVar_hsa_circ_224054,RMVar_hsa_circ_364505,RMVar_hsa_circ_346282,RMVar_hsa_circ_334808,RMVar_hsa_circ_304711,RMVar_hsa_circ_312883,RMVar_hsa_circ_296549,RMVar_hsa_circ_279707,RMVar_hsa_circ_283600,RMVar_hsa_circ_224056,RMVar_hsa_circ_224060,RMVar_hsa_circ_224064,RMVar_hsa_circ_7799,RMVar_hsa_circ_22209,RMVar_hsa_circ_224065,RMVar_hsa_circ_224062,RMVar_hsa_circ_224063,RMVar_hsa_circ_224061,RMVar_hsa_circ_224058,RMVar_hsa_circ_224059,RMVar_hsa_circ_224057,RMVar_hsa_circ_66150,RMVar_hsa_circ_106997,RMVar_hsa_circ_274950,RMVar_hsa_circ_224055,RMVar_hsa_circ_372829,RMVar_hsa_circ_267518,RMVar_hsa_circ_72387,RMVar_hsa_circ_224067,RMVar_hsa_circ_224069,RMVar_hsa_circ_224068 32575 RMVar_ID_32575 Human_SNP_ID_169924256 A-to-I Human chr3 + 197818970 197818970 197818970 CAACATAGTGAAACCCCATCTCTGCTAAAAATACAAAAATTAGCCAGGCGTGGTGGCACGCACCT CAACATAGTGAAACCCCATCTCTGCTAAAAATTCAAAAATTAGCCAGGCGTGGTGGCACGCACCT A T LRCH3 Ensembl:ENSG00000186001 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1258160241 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_53166,RMVar_hsa_circ_224053,RMVar_hsa_circ_268217,RMVar_hsa_circ_294903,RMVar_hsa_circ_316087,RMVar_hsa_circ_340719,RMVar_hsa_circ_362064,RMVar_hsa_circ_224054,RMVar_hsa_circ_364505,RMVar_hsa_circ_346282,RMVar_hsa_circ_334808,RMVar_hsa_circ_304711,RMVar_hsa_circ_312883,RMVar_hsa_circ_296549,RMVar_hsa_circ_279707,RMVar_hsa_circ_283600,RMVar_hsa_circ_224056,RMVar_hsa_circ_224060,RMVar_hsa_circ_224064,RMVar_hsa_circ_7799,RMVar_hsa_circ_22209,RMVar_hsa_circ_224065,RMVar_hsa_circ_224062,RMVar_hsa_circ_224063,RMVar_hsa_circ_224061,RMVar_hsa_circ_224058,RMVar_hsa_circ_224059,RMVar_hsa_circ_224057,RMVar_hsa_circ_66150,RMVar_hsa_circ_106997,RMVar_hsa_circ_274950,RMVar_hsa_circ_224055,RMVar_hsa_circ_372829,RMVar_hsa_circ_267518,RMVar_hsa_circ_72387,RMVar_hsa_circ_224067,RMVar_hsa_circ_224069,RMVar_hsa_circ_224068 32576 RMVar_ID_32576 Human_SNP_ID_169924267 A-to-I Human chr3 + 197818995 197818995 197818995 TAAAAATACAAAAATTAGCCAGGCGTGGTGGCACGCACCTGTTATCCCAGCAACTTGGGAGGCTG TAAAAATACAAAAATTAGCCAGGCGTGGTGGCCCGCACCTGTTATCCCAGCAACTTGGGAGGCTG A C LRCH3 Ensembl:ENSG00000186001 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs942060597 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_53166,RMVar_hsa_circ_224053,RMVar_hsa_circ_268217,RMVar_hsa_circ_294903,RMVar_hsa_circ_316087,RMVar_hsa_circ_340719,RMVar_hsa_circ_362064,RMVar_hsa_circ_224054,RMVar_hsa_circ_364505,RMVar_hsa_circ_346282,RMVar_hsa_circ_334808,RMVar_hsa_circ_304711,RMVar_hsa_circ_312883,RMVar_hsa_circ_296549,RMVar_hsa_circ_279707,RMVar_hsa_circ_283600,RMVar_hsa_circ_224056,RMVar_hsa_circ_224060,RMVar_hsa_circ_224064,RMVar_hsa_circ_7799,RMVar_hsa_circ_22209,RMVar_hsa_circ_224065,RMVar_hsa_circ_224062,RMVar_hsa_circ_224063,RMVar_hsa_circ_224061,RMVar_hsa_circ_224058,RMVar_hsa_circ_224059,RMVar_hsa_circ_224057,RMVar_hsa_circ_66150,RMVar_hsa_circ_106997,RMVar_hsa_circ_274950,RMVar_hsa_circ_224055,RMVar_hsa_circ_372829,RMVar_hsa_circ_267518,RMVar_hsa_circ_72387,RMVar_hsa_circ_224067,RMVar_hsa_circ_224069,RMVar_hsa_circ_224068 32577 RMVar_ID_32577 Human_SNP_ID_169924272 A-to-I Human chr3 + 197818999 197818999 197818999 AATACAAAAATTAGCCAGGCGTGGTGGCACGCACCTGTTATCCCAGCAACTTGGGAGGCTGAGGC AATACAAAAATTAGCCAGGCGTGGTGGCACGCCCCTGTTATCCCAGCAACTTGGGAGGCTGAGGC A C LRCH3 Ensembl:ENSG00000186001 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs905950722 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_53166,RMVar_hsa_circ_224053,RMVar_hsa_circ_268217,RMVar_hsa_circ_294903,RMVar_hsa_circ_316087,RMVar_hsa_circ_340719,RMVar_hsa_circ_362064,RMVar_hsa_circ_224054,RMVar_hsa_circ_364505,RMVar_hsa_circ_346282,RMVar_hsa_circ_334808,RMVar_hsa_circ_304711,RMVar_hsa_circ_312883,RMVar_hsa_circ_296549,RMVar_hsa_circ_279707,RMVar_hsa_circ_283600,RMVar_hsa_circ_224056,RMVar_hsa_circ_224060,RMVar_hsa_circ_224064,RMVar_hsa_circ_7799,RMVar_hsa_circ_22209,RMVar_hsa_circ_224065,RMVar_hsa_circ_224062,RMVar_hsa_circ_224063,RMVar_hsa_circ_224061,RMVar_hsa_circ_224058,RMVar_hsa_circ_224059,RMVar_hsa_circ_224057,RMVar_hsa_circ_66150,RMVar_hsa_circ_106997,RMVar_hsa_circ_274950,RMVar_hsa_circ_224055,RMVar_hsa_circ_372829,RMVar_hsa_circ_267518,RMVar_hsa_circ_72387,RMVar_hsa_circ_224067,RMVar_hsa_circ_224069,RMVar_hsa_circ_224068 32578 RMVar_ID_32578 Human_SNP_ID_169928762 A-to-I Human chr3 + 197835033 197835033 197835033 GGGCGTGGTGGTGCACACCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAA GGGCGTGGTGGTGCACACCTGTAATCCCAGCTCCTTGGGAGGCTGAGGCAGGAGAATCGCTTGAA A C LRCH3 Ensembl:ENSG00000186001 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs980567410 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23067,RMVar_hsa_circ_53166,RMVar_hsa_circ_268217,RMVar_hsa_circ_294903,RMVar_hsa_circ_316087,RMVar_hsa_circ_340719,RMVar_hsa_circ_362064,RMVar_hsa_circ_364505,RMVar_hsa_circ_346282,RMVar_hsa_circ_334808,RMVar_hsa_circ_224056,RMVar_hsa_circ_224060,RMVar_hsa_circ_7799,RMVar_hsa_circ_22209,RMVar_hsa_circ_224058,RMVar_hsa_circ_224059,RMVar_hsa_circ_224057,RMVar_hsa_circ_66150,RMVar_hsa_circ_224055,RMVar_hsa_circ_372829,RMVar_hsa_circ_224067,RMVar_hsa_circ_61826,RMVar_hsa_circ_29559,RMVar_hsa_circ_224082,RMVar_hsa_circ_27842,RMVar_hsa_circ_121931,RMVar_hsa_circ_224075,RMVar_hsa_circ_363910,RMVar_hsa_circ_98288,RMVar_hsa_circ_224076,RMVar_hsa_circ_34229,RMVar_hsa_circ_41674,RMVar_hsa_circ_224077,RMVar_hsa_circ_292776,RMVar_hsa_circ_315514,RMVar_hsa_circ_354643,RMVar_hsa_circ_366423,RMVar_hsa_circ_330706,RMVar_hsa_circ_296192,RMVar_hsa_circ_92633,RMVar_hsa_circ_273022,RMVar_hsa_circ_224078,RMVar_hsa_circ_224079,RMVar_hsa_circ_224080,RMVar_hsa_circ_305690,RMVar_hsa_circ_315988,RMVar_hsa_circ_337778,RMVar_hsa_circ_285973,RMVar_hsa_circ_272172,RMVar_hsa_circ_117001,RMVar_hsa_circ_224086,RMVar_hsa_circ_224088,RMVar_hsa_circ_83112,RMVar_hsa_circ_224089,RMVar_hsa_circ_224087,RMVar_hsa_circ_224084,RMVar_hsa_circ_224085,RMVar_hsa_circ_224083,RMVar_hsa_circ_224091,RMVar_hsa_circ_280656,RMVar_hsa_circ_322212,RMVar_hsa_circ_331636,RMVar_hsa_circ_224081,RMVar_hsa_circ_371637,RMVar_hsa_circ_327093,RMVar_hsa_circ_292508,RMVar_hsa_circ_44190,RMVar_hsa_circ_269586,RMVar_hsa_circ_224093,RMVar_hsa_circ_224094,RMVar_hsa_circ_224092 32579 RMVar_ID_32579 Human_SNP_ID_169928763 A-to-I Human chr3 + 197835033 197835033 197835033 GGGCGTGGTGGTGCACACCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAA GGGCGTGGTGGTGCACACCTGTAATCCCAGCTGCTTGGGAGGCTGAGGCAGGAGAATCGCTTGAA A G LRCH3 Ensembl:ENSG00000186001 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs980567410 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23067,RMVar_hsa_circ_53166,RMVar_hsa_circ_268217,RMVar_hsa_circ_294903,RMVar_hsa_circ_316087,RMVar_hsa_circ_340719,RMVar_hsa_circ_362064,RMVar_hsa_circ_364505,RMVar_hsa_circ_346282,RMVar_hsa_circ_334808,RMVar_hsa_circ_224056,RMVar_hsa_circ_224060,RMVar_hsa_circ_7799,RMVar_hsa_circ_22209,RMVar_hsa_circ_224058,RMVar_hsa_circ_224059,RMVar_hsa_circ_224057,RMVar_hsa_circ_66150,RMVar_hsa_circ_224055,RMVar_hsa_circ_372829,RMVar_hsa_circ_224067,RMVar_hsa_circ_61826,RMVar_hsa_circ_29559,RMVar_hsa_circ_224082,RMVar_hsa_circ_27842,RMVar_hsa_circ_121931,RMVar_hsa_circ_224075,RMVar_hsa_circ_363910,RMVar_hsa_circ_98288,RMVar_hsa_circ_224076,RMVar_hsa_circ_34229,RMVar_hsa_circ_41674,RMVar_hsa_circ_224077,RMVar_hsa_circ_292776,RMVar_hsa_circ_315514,RMVar_hsa_circ_354643,RMVar_hsa_circ_366423,RMVar_hsa_circ_330706,RMVar_hsa_circ_296192,RMVar_hsa_circ_92633,RMVar_hsa_circ_273022,RMVar_hsa_circ_224078,RMVar_hsa_circ_224079,RMVar_hsa_circ_224080,RMVar_hsa_circ_305690,RMVar_hsa_circ_315988,RMVar_hsa_circ_337778,RMVar_hsa_circ_285973,RMVar_hsa_circ_272172,RMVar_hsa_circ_117001,RMVar_hsa_circ_224086,RMVar_hsa_circ_224088,RMVar_hsa_circ_83112,RMVar_hsa_circ_224089,RMVar_hsa_circ_224087,RMVar_hsa_circ_224084,RMVar_hsa_circ_224085,RMVar_hsa_circ_224083,RMVar_hsa_circ_224091,RMVar_hsa_circ_280656,RMVar_hsa_circ_322212,RMVar_hsa_circ_331636,RMVar_hsa_circ_224081,RMVar_hsa_circ_371637,RMVar_hsa_circ_327093,RMVar_hsa_circ_292508,RMVar_hsa_circ_44190,RMVar_hsa_circ_269586,RMVar_hsa_circ_224093,RMVar_hsa_circ_224094,RMVar_hsa_circ_224092 32580 RMVar_ID_32580 Human_SNP_ID_169928900 A-to-I Human chr3 + 197835367 197835367 197835367 CACTAAGCCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGATTTCAGCATATTGGTCAGGCTTG CACTAAGCCCAGCTAATTTTTGTATTTTTAGTGGAGACGGGATTTCAGCATATTGGTCAGGCTTG A G LRCH3 Ensembl:ENSG00000186001 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs111879607 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23067,RMVar_hsa_circ_53166,RMVar_hsa_circ_268217,RMVar_hsa_circ_294903,RMVar_hsa_circ_316087,RMVar_hsa_circ_340719,RMVar_hsa_circ_362064,RMVar_hsa_circ_364505,RMVar_hsa_circ_346282,RMVar_hsa_circ_334808,RMVar_hsa_circ_224056,RMVar_hsa_circ_224060,RMVar_hsa_circ_7799,RMVar_hsa_circ_22209,RMVar_hsa_circ_224058,RMVar_hsa_circ_224059,RMVar_hsa_circ_224057,RMVar_hsa_circ_66150,RMVar_hsa_circ_224055,RMVar_hsa_circ_372829,RMVar_hsa_circ_224067,RMVar_hsa_circ_61826,RMVar_hsa_circ_29559,RMVar_hsa_circ_224082,RMVar_hsa_circ_27842,RMVar_hsa_circ_121931,RMVar_hsa_circ_224075,RMVar_hsa_circ_363910,RMVar_hsa_circ_98288,RMVar_hsa_circ_224076,RMVar_hsa_circ_34229,RMVar_hsa_circ_41674,RMVar_hsa_circ_224077,RMVar_hsa_circ_292776,RMVar_hsa_circ_315514,RMVar_hsa_circ_354643,RMVar_hsa_circ_366423,RMVar_hsa_circ_330706,RMVar_hsa_circ_296192,RMVar_hsa_circ_92633,RMVar_hsa_circ_273022,RMVar_hsa_circ_224078,RMVar_hsa_circ_224079,RMVar_hsa_circ_224080,RMVar_hsa_circ_305690,RMVar_hsa_circ_315988,RMVar_hsa_circ_337778,RMVar_hsa_circ_285973,RMVar_hsa_circ_272172,RMVar_hsa_circ_117001,RMVar_hsa_circ_224086,RMVar_hsa_circ_224088,RMVar_hsa_circ_83112,RMVar_hsa_circ_224089,RMVar_hsa_circ_224087,RMVar_hsa_circ_224084,RMVar_hsa_circ_224085,RMVar_hsa_circ_224083,RMVar_hsa_circ_224091,RMVar_hsa_circ_280656,RMVar_hsa_circ_322212,RMVar_hsa_circ_331636,RMVar_hsa_circ_224081,RMVar_hsa_circ_371637,RMVar_hsa_circ_327093,RMVar_hsa_circ_292508,RMVar_hsa_circ_44190,RMVar_hsa_circ_269586,RMVar_hsa_circ_224093,RMVar_hsa_circ_224094,RMVar_hsa_circ_224092 32581 RMVar_ID_32581 Human_SNP_ID_169929323 A-to-I Human chr3 + 197836752 197836752 197836752 CAGGCTGGTGTGCCTTGGCACGATCTCGGCTTACTGCAGCCTCTGCCTCCCAGGTTCAAGTGATT CAGGCTGGTGTGCCTTGGCACGATCTCGGCTTGCTGCAGCCTCTGCCTCCCAGGTTCAAGTGATT A G LRCH3 Ensembl:ENSG00000186001 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs962732191 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23067,RMVar_hsa_circ_53166,RMVar_hsa_circ_268217,RMVar_hsa_circ_294903,RMVar_hsa_circ_316087,RMVar_hsa_circ_340719,RMVar_hsa_circ_364505,RMVar_hsa_circ_346282,RMVar_hsa_circ_334808,RMVar_hsa_circ_224056,RMVar_hsa_circ_224060,RMVar_hsa_circ_7799,RMVar_hsa_circ_22209,RMVar_hsa_circ_224058,RMVar_hsa_circ_224059,RMVar_hsa_circ_224057,RMVar_hsa_circ_66150,RMVar_hsa_circ_224055,RMVar_hsa_circ_372829,RMVar_hsa_circ_224067,RMVar_hsa_circ_61826,RMVar_hsa_circ_29559,RMVar_hsa_circ_224082,RMVar_hsa_circ_121931,RMVar_hsa_circ_224075,RMVar_hsa_circ_363910,RMVar_hsa_circ_98288,RMVar_hsa_circ_224076,RMVar_hsa_circ_34229,RMVar_hsa_circ_224077,RMVar_hsa_circ_292776,RMVar_hsa_circ_315514,RMVar_hsa_circ_354643,RMVar_hsa_circ_366423,RMVar_hsa_circ_330706,RMVar_hsa_circ_296192,RMVar_hsa_circ_92633,RMVar_hsa_circ_273022,RMVar_hsa_circ_224078,RMVar_hsa_circ_224079,RMVar_hsa_circ_224080,RMVar_hsa_circ_305690,RMVar_hsa_circ_337778,RMVar_hsa_circ_285973,RMVar_hsa_circ_272172,RMVar_hsa_circ_117001,RMVar_hsa_circ_224086,RMVar_hsa_circ_224088,RMVar_hsa_circ_83112,RMVar_hsa_circ_224087,RMVar_hsa_circ_224084,RMVar_hsa_circ_224085,RMVar_hsa_circ_224083,RMVar_hsa_circ_224095,RMVar_hsa_circ_322212,RMVar_hsa_circ_331636,RMVar_hsa_circ_224081,RMVar_hsa_circ_371637,RMVar_hsa_circ_327093,RMVar_hsa_circ_292508,RMVar_hsa_circ_269586,RMVar_hsa_circ_224093,RMVar_hsa_circ_224094,RMVar_hsa_circ_224092,RMVar_hsa_circ_224099,RMVar_hsa_circ_321963,RMVar_hsa_circ_357953,RMVar_hsa_circ_373205,RMVar_hsa_circ_346909,RMVar_hsa_circ_318474,RMVar_hsa_circ_224097,RMVar_hsa_circ_224098,RMVar_hsa_circ_224096 32582 RMVar_ID_32582 Human_SNP_ID_169931857 A-to-I Human chr3 + 197845264 197845264 197845264 AACCCCATCTCTACCAAAAATAGATGAAAATTAGCCAGGCATGGTGGTGCACACCTGTAGTTCCA AACCCCATCTCTACCAAAAATAGATGAAAATTGGCCAGGCATGGTGGTGCACACCTGTAGTTCCA A G LRCH3 Ensembl:ENSG00000186001 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1340797174 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23067,RMVar_hsa_circ_53166,RMVar_hsa_circ_268217,RMVar_hsa_circ_294903,RMVar_hsa_circ_316087,RMVar_hsa_circ_364505,RMVar_hsa_circ_346282,RMVar_hsa_circ_334808,RMVar_hsa_circ_224056,RMVar_hsa_circ_7799,RMVar_hsa_circ_22209,RMVar_hsa_circ_224058,RMVar_hsa_circ_224059,RMVar_hsa_circ_224057,RMVar_hsa_circ_224055,RMVar_hsa_circ_372829,RMVar_hsa_circ_224067,RMVar_hsa_circ_61826,RMVar_hsa_circ_29559,RMVar_hsa_circ_224082,RMVar_hsa_circ_121931,RMVar_hsa_circ_98288,RMVar_hsa_circ_224076,RMVar_hsa_circ_34229,RMVar_hsa_circ_224077,RMVar_hsa_circ_292776,RMVar_hsa_circ_315514,RMVar_hsa_circ_354643,RMVar_hsa_circ_366423,RMVar_hsa_circ_330706,RMVar_hsa_circ_92633,RMVar_hsa_circ_273022,RMVar_hsa_circ_224079,RMVar_hsa_circ_224080,RMVar_hsa_circ_305690,RMVar_hsa_circ_337778,RMVar_hsa_circ_285973,RMVar_hsa_circ_117001,RMVar_hsa_circ_224086,RMVar_hsa_circ_83112,RMVar_hsa_circ_224087,RMVar_hsa_circ_224084,RMVar_hsa_circ_224085,RMVar_hsa_circ_224083,RMVar_hsa_circ_224095,RMVar_hsa_circ_322212,RMVar_hsa_circ_331636,RMVar_hsa_circ_224081,RMVar_hsa_circ_371637,RMVar_hsa_circ_292508,RMVar_hsa_circ_269586,RMVar_hsa_circ_224093,RMVar_hsa_circ_224094,RMVar_hsa_circ_357953,RMVar_hsa_circ_373205,RMVar_hsa_circ_346909,RMVar_hsa_circ_318474,RMVar_hsa_circ_224097,RMVar_hsa_circ_224098,RMVar_hsa_circ_224096,RMVar_hsa_circ_224101,RMVar_hsa_circ_118903,RMVar_hsa_circ_310187,RMVar_hsa_circ_357969,RMVar_hsa_circ_374520,RMVar_hsa_circ_355646,RMVar_hsa_circ_306724,RMVar_hsa_circ_224102,RMVar_hsa_circ_224100 32583 RMVar_ID_32583 Human_SNP_ID_169936559 A-to-I Human chr3 + 197864421 197864421 197864421 CCTGAGGTTGGGAGTTCGAGAACGGCCTGACTAACATGGAGAAACCCCGTATCTACTAAAAATAC CCTGAGGTTGGGAGTTCGAGAACGGCCTGACTCACATGGAGAAACCCCGTATCTACTAAAAATAC A C LRCH3 Ensembl:ENSG00000186001 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042103258 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14769807 RMVar_hsa_circ_23067,RMVar_hsa_circ_53166,RMVar_hsa_circ_316087,RMVar_hsa_circ_346282,RMVar_hsa_circ_224056,RMVar_hsa_circ_22209,RMVar_hsa_circ_224055,RMVar_hsa_circ_61826,RMVar_hsa_circ_224082,RMVar_hsa_circ_121931,RMVar_hsa_circ_98288,RMVar_hsa_circ_224076,RMVar_hsa_circ_224077,RMVar_hsa_circ_292776,RMVar_hsa_circ_315514,RMVar_hsa_circ_366423,RMVar_hsa_circ_92633,RMVar_hsa_circ_273022,RMVar_hsa_circ_224079,RMVar_hsa_circ_224080,RMVar_hsa_circ_305690,RMVar_hsa_circ_337778,RMVar_hsa_circ_224084,RMVar_hsa_circ_224083,RMVar_hsa_circ_224095,RMVar_hsa_circ_322212,RMVar_hsa_circ_331636,RMVar_hsa_circ_224081,RMVar_hsa_circ_371637,RMVar_hsa_circ_269586,RMVar_hsa_circ_224094,RMVar_hsa_circ_373205,RMVar_hsa_circ_346909,RMVar_hsa_circ_318474,RMVar_hsa_circ_224097,RMVar_hsa_circ_224096,RMVar_hsa_circ_82140,RMVar_hsa_circ_112858,RMVar_hsa_circ_224101,RMVar_hsa_circ_118903,RMVar_hsa_circ_310187,RMVar_hsa_circ_355646,RMVar_hsa_circ_224102,RMVar_hsa_circ_314726,RMVar_hsa_circ_284116,RMVar_hsa_circ_12802,RMVar_hsa_circ_224103,RMVar_hsa_circ_224105,RMVar_hsa_circ_224104,RMVar_hsa_circ_224107,RMVar_hsa_circ_80431,RMVar_hsa_circ_310805,RMVar_hsa_circ_224109,RMVar_hsa_circ_112676,RMVar_hsa_circ_324628,RMVar_hsa_circ_224108,RMVar_hsa_circ_315759,RMVar_hsa_circ_114157,RMVar_hsa_circ_287308,RMVar_hsa_circ_224112,RMVar_hsa_circ_224114,RMVar_hsa_circ_224115,RMVar_hsa_circ_224113,RMVar_hsa_circ_224111 32584 RMVar_ID_32584 Human_SNP_ID_169939243 A-to-I Human chr3 + 197873910 197873910 197873910 GTGCATGGTGGTGCACACCTGTAGTCCCAGCTACTTGGGAGGCAGAAGCAGGAGAATCACTTGAG GTGCATGGTGGTGCACACCTGTAGTCCCAGCTGCTTGGGAGGCAGAAGCAGGAGAATCACTTGAG A G LRCH3 Ensembl:ENSG00000186001 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs771908326 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_316087,RMVar_hsa_circ_22209,RMVar_hsa_circ_224055,RMVar_hsa_circ_61826,RMVar_hsa_circ_98288,RMVar_hsa_circ_224076,RMVar_hsa_circ_366423,RMVar_hsa_circ_371637,RMVar_hsa_circ_224094,RMVar_hsa_circ_355646,RMVar_hsa_circ_284116,RMVar_hsa_circ_12802,RMVar_hsa_circ_224103,RMVar_hsa_circ_310805,RMVar_hsa_circ_224115,RMVar_hsa_circ_270188,RMVar_hsa_circ_224119,RMVar_hsa_circ_224120,RMVar_hsa_circ_331862,RMVar_hsa_circ_224124,RMVar_hsa_circ_275340,RMVar_hsa_circ_39080 32585 RMVar_ID_32585 Human_SNP_ID_169939540 A-to-I Human chr3 + 197875108 197875108 197875108 GCCCGCCACCACACCTGGCTAATTTTTGTATTATTAGTAGAGACGGGGTTTCTCCATGTTCGTCA GCCCGCCACCACACCTGGCTAATTTTTGTATTCTTAGTAGAGACGGGGTTTCTCCATGTTCGTCA A C LRCH3 Ensembl:ENSG00000186001 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1219550448 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_316087,RMVar_hsa_circ_22209,RMVar_hsa_circ_224055,RMVar_hsa_circ_61826,RMVar_hsa_circ_98288,RMVar_hsa_circ_224076,RMVar_hsa_circ_366423,RMVar_hsa_circ_371637,RMVar_hsa_circ_224094,RMVar_hsa_circ_355646,RMVar_hsa_circ_284116,RMVar_hsa_circ_12802,RMVar_hsa_circ_224103,RMVar_hsa_circ_310805,RMVar_hsa_circ_224115,RMVar_hsa_circ_270188,RMVar_hsa_circ_224119,RMVar_hsa_circ_224120,RMVar_hsa_circ_331862,RMVar_hsa_circ_224124,RMVar_hsa_circ_275340,RMVar_hsa_circ_39080 32586 RMVar_ID_32586 Human_SNP_ID_169939659 A-to-I Human chr3 + 197875533 197875533 197875533 AAAATTGCCCAGGTGTGATGGCATGCAACTATAGTCCCAGCTACTTGGGAGGCTGAGGTGGGAGG AAAATTGCCCAGGTGTGATGGCATGCAACTATCGTCCCAGCTACTTGGGAGGCTGAGGTGGGAGG A C LRCH3 Ensembl:ENSG00000186001 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs140023763 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_316087,RMVar_hsa_circ_22209,RMVar_hsa_circ_224055,RMVar_hsa_circ_61826,RMVar_hsa_circ_98288,RMVar_hsa_circ_224076,RMVar_hsa_circ_366423,RMVar_hsa_circ_371637,RMVar_hsa_circ_224094,RMVar_hsa_circ_355646,RMVar_hsa_circ_284116,RMVar_hsa_circ_12802,RMVar_hsa_circ_224103,RMVar_hsa_circ_310805,RMVar_hsa_circ_224115,RMVar_hsa_circ_270188,RMVar_hsa_circ_224119,RMVar_hsa_circ_224120,RMVar_hsa_circ_331862,RMVar_hsa_circ_224124,RMVar_hsa_circ_275340,RMVar_hsa_circ_39080 32587 RMVar_ID_32587 Human_SNP_ID_169942346 A-to-I Human chr3 + 197884176 197884171 197884177 AACCATTGCACATGTTTTTGTTTTTGTTGGAGAAGGAGTTCTGCTCAGTCGCCCAGGCTAGAGTG AACCATTGCACATGTTTTTGTTTTTGTT______GGAGTTCTGCTCAGTCGCCCAGGCTAGAGTG TGGAGAA T LRCH3 Ensembl:ENSG00000186001 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1040423725 Functional Loss DEL dbSNP153 29..34 33 - - - Human_RBP_ID_159183,Human_RBP_ID_2775826,Human_RBP_ID_3702611,Human_RBP_ID_7179250,Human_RBP_ID_14770011,Human_RBP_ID_26683339 32588 RMVar_ID_32588 Human_SNP_ID_169942353 A-to-I Human chr3 + 197884190 197884190 197884190 TTTTTGTTTTTGTTGGAGAAGGAGTTCTGCTCAGTCGCCCAGGCTAGAGTGCAGTGGCATAATCT TTTTTGTTTTTGTTGGAGAAGGAGTTCTGCTCTGTCGCCCAGGCTAGAGTGCAGTGGCATAATCT A T LRCH3 Ensembl:ENSG00000186001 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978564590 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2775826 32589 RMVar_ID_32589 Human_SNP_ID_169942360 A-to-I Human chr3 + 197884203 197884203 197884203 TGGAGAAGGAGTTCTGCTCAGTCGCCCAGGCTAGAGTGCAGTGGCATAATCTCAGCTCACTGCAA TGGAGAAGGAGTTCTGCTCAGTCGCCCAGGCTGGAGTGCAGTGGCATAATCTCAGCTCACTGCAA A G LRCH3 Ensembl:ENSG00000186001 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs144715213 Functional Loss SNV dbSNP153 33..33 33 - - - 32590 RMVar_ID_32590 Human_SNP_ID_169942363 A-to-I Human chr3 + 197884218 197884218 197884218 GCTCAGTCGCCCAGGCTAGAGTGCAGTGGCATAATCTCAGCTCACTGCAACCTCCGCCTCCCGGG GCTCAGTCGCCCAGGCTAGAGTGCAGTGGCATCATCTCAGCTCACTGCAACCTCCGCCTCCCGGG A C LRCH3 Ensembl:ENSG00000186001 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs1023186781 Functional Loss SNV dbSNP153 33..33 33 - - - 32591 RMVar_ID_32591 Human_SNP_ID_169942411 A-to-I Human chr3 + 197884418 197884418 197884418 ACTTCAAGTGATCCACCTGCCTCGGCCTCCCAAAATGCTGGGATTACAGGCGTGAGCCACTGTGC ACTTCAAGTGATCCACCTGCCTCGGCCTCCCAGAATGCTGGGATTACAGGCGTGAGCCACTGTGC A G LRCH3 Ensembl:ENSG00000186001 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1316295707 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17573974 32592 RMVar_ID_32592 Human_SNP_ID_169942412 A-to-I Human chr3 + 197884419 197884419 197884419 CTTCAAGTGATCCACCTGCCTCGGCCTCCCAAAATGCTGGGATTACAGGCGTGAGCCACTGTGCC CTTCAAGTGATCCACCTGCCTCGGCCTCCCAAGATGCTGGGATTACAGGCGTGAGCCACTGTGCC A G LRCH3 Ensembl:ENSG00000186001 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs368150146 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17573974 32593 RMVar_ID_32593 Human_SNP_ID_169942437 A-to-I Human chr3 + 197884461 197884461 197884461 TTACAGGCGTGAGCCACTGTGCCCGGCCTCCCAGAGTGCTGGGATGACAGGCGTGAGCCCCCGCG TTACAGGCGTGAGCCACTGTGCCCGGCCTCCCGGAGTGCTGGGATGACAGGCGTGAGCCCCCGCG A G LRCH3 Ensembl:ENSG00000186001 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1243604652 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_784858,Human_RBP_ID_17573974,Human_RBP_ID_26771127 32594 RMVar_ID_32594 Human_SNP_ID_169942718 A-to-I Human chr3 + 197885349 197885349 197885349 CAGCATCTTCCTAGCTGGGTGTGGTGGCTCACACCTGTAATCTCAGCACTTTGGGAGGCTGAGGC CAGCATCTTCCTAGCTGGGTGTGGTGGCTCACGCCTGTAATCTCAGCACTTTGGGAGGCTGAGGC A G LRCH3 Ensembl:ENSG00000186001 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs373565572 Functional Loss SNV dbSNP153 33..33 33 - - - 32595 RMVar_ID_32595 Human_SNP_ID_169942719 A-to-I Human chr3 + 197885349 197885349 197885349 CAGCATCTTCCTAGCTGGGTGTGGTGGCTCACACCTGTAATCTCAGCACTTTGGGAGGCTGAGGC CAGCATCTTCCTAGCTGGGTGTGGTGGCTCACTCCTGTAATCTCAGCACTTTGGGAGGCTGAGGC A T LRCH3 Ensembl:ENSG00000186001 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs373565572 Functional Loss SNV dbSNP153 33..33 33 - - - 32596 RMVar_ID_32596 Human_SNP_ID_169942773 A-to-I Human chr3 + 197885559 197885559 197885559 TTGAACCCAGGAGGCGGAGGTTGTGGTGAGCCAAGATCGTGCCATTGCACCCCAGCCTGGGCAAC TTGAACCCAGGAGGCGGAGGTTGTGGTGAGCCGAGATCGTGCCATTGCACCCCAGCCTGGGCAAC A G LRCH3 Ensembl:ENSG00000186001 Protein coding 3'UTR GSE38233;GSE100210;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,29129909,31158229 RNA-Seq:(High) rs372007347 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25727117 32597 RMVar_ID_32597 Human_SNP_ID_169943068 A-to-I Human chr3 + 197886658 197886658 197886658 GAAACCTTGTCTCTACTAAAAATACAAAAATTAGCTGGGCGTGGTGGTGGGCACCTGTAATCCCA GAAACCTTGTCTCTACTAAAAATACAAAAATTGGCTGGGCGTGGTGGTGGGCACCTGTAATCCCA A G LRCH3 Ensembl:ENSG00000186001 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs1415580010 Functional Loss SNV dbSNP153 33..33 33 - - - 32598 RMVar_ID_32598 Human_SNP_ID_169943079 A-to-I Human chr3 + 197886684 197886684 197886684 AAAATTAGCTGGGCGTGGTGGTGGGCACCTGTAATCCCAGCTACTTGGGTGGCTGAGGCACAAGA AAAATTAGCTGGGCGTGGTGGTGGGCACCTGTCATCCCAGCTACTTGGGTGGCTGAGGCACAAGA A C LRCH3 Ensembl:ENSG00000186001 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1222323054 Functional Loss SNV dbSNP153 33..33 33 - - - 32599 RMVar_ID_32599 Human_SNP_ID_169949058 A-to-I Human chr3 - 197909884 197909884 197909884 CAGGTTCAAGTGATTCTCCTGCCAGCCTCCCGAGTAGCTGGGATTACATGCACCTGCCACCACAC CAGGTTCAAGTGATTCTCCTGCCAGCCTCCCGTGTAGCTGGGATTACATGCACCTGCCACCACAC T A IQCG Ensembl:ENSG00000114473 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1014519226 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14770062 RMVar_hsa_circ_10761 32600 RMVar_ID_32600 Human_SNP_ID_169949081 A-to-I Human chr3 - 197909951 197909951 197909951 GAGTCTTGCTCTGTTGCCCAGGCTGGAGTGCAATGGCGCGATCTCGGCTCACTGCAACCTCTGCC GAGTCTTGCTCTGTTGCCCAGGCTGGAGTGCAGTGGCGCGATCTCGGCTCACTGCAACCTCTGCC T C IQCG Ensembl:ENSG00000114473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs562294726 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10761 32601 RMVar_ID_32601 Human_SNP_ID_169949581 A-to-I Human chr3 - 197912178 197912178 197912178 AAAAATTAGCCGGGCATGGTGGTGCGCCTGTAATCCCAGCTATTCAGGAGGCTGAGGTGGGAGAA AAAAATTAGCCGGGCATGGTGGTGCGCCTGTAGTCCCAGCTATTCAGGAGGCTGAGGTGGGAGAA T C IQCG Ensembl:ENSG00000114473 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1367265438 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10761 32602 RMVar_ID_32602 Human_SNP_ID_169949582 A-to-I Human chr3 - 197912179 197912179 197912179 CAAAAATTAGCCGGGCATGGTGGTGCGCCTGTAATCCCAGCTATTCAGGAGGCTGAGGTGGGAGA CAAAAATTAGCCGGGCATGGTGGTGCGCCTGTTATCCCAGCTATTCAGGAGGCTGAGGTGGGAGA T A IQCG Ensembl:ENSG00000114473 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1219704551 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10761 32603 RMVar_ID_32603 Human_SNP_ID_169962001 A-to-I Human chr3 - 197957525 197957524 197957525 TGAACCCGGGAGGCGGAGCGTGCAGTGAGCCAAGATTGCGCCACTGCACTCCAGCCTAGACGACA TGAACCCGGGAGGCGGAGCGTGCAGTGAGCCA_GATTGCGCCACTGCACTCCAGCCTAGACGACA CT C IQCG Ensembl:ENSG00000114473 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1485471681 Functional Loss DEL dbSNP153 33..33 33 - - - 32604 RMVar_ID_32604 Human_SNP_ID_169962002 A-to-I Human chr3 - 197957526 197957526 197957526 GTGAACCCGGGAGGCGGAGCGTGCAGTGAGCCAAGATTGCGCCACTGCACTCCAGCCTAGACGAC GTGAACCCGGGAGGCGGAGCGTGCAGTGAGCCGAGATTGCGCCACTGCACTCCAGCCTAGACGAC T C IQCG Ensembl:ENSG00000114473 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1188763050 Functional Loss SNV dbSNP153 33..33 33 - - - 32605 RMVar_ID_32605 Human_SNP_ID_169978598 A-to-I Human chr3 + 198026475 198026474 198026475 GCACAGCTGGAATCACAGGCATGCGCCACCATACCCAGCTAATTTTTGTATTTTTAGTACAAAAA GCACAGCTGGAATCACAGGCATGCGCCACCAT_CCCAGCTAATTTTTGTATTTTTAGTACAAAAA TA T LMLN Ensembl:ENSG00000185621 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1428977826 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_269052,RMVar_hsa_circ_64359,RMVar_hsa_circ_361756 32606 RMVar_ID_32606 Human_SNP_ID_311596729 A-to-I Human chr7 - 16089229 16089202 16089230 ACGCATACACACATATATGTATATACGTACGCATACACACATATATGTATATACGTACGTATATA ACGCATACACACATATATGTATATACGTACG____________________________TATATA ACGTACGTATATACATATATGTGTGTATG A CRPPA Ensembl:ENSG00000214960 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1554267125 Functional Loss DEL dbSNP153 32..59 33 - - - RMVar_hsa_circ_112717,RMVar_hsa_circ_116458,RMVar_hsa_circ_243875,RMVar_hsa_circ_243876 32607 RMVar_ID_32607 Human_SNP_ID_311596736 A-to-I Human chr7 - 16089209 16089209 16089209 ATATACGTACGCATACACACATATATGTATATACGTACGTATATACACACATATATGTATATACG ATATACGTACGCATACACACATATATGTATATGCGTACGTATATACACACATATATGTATATACG T C CRPPA Ensembl:ENSG00000214960 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs995512667 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112717,RMVar_hsa_circ_116458,RMVar_hsa_circ_243875,RMVar_hsa_circ_243876 32608 RMVar_ID_32608 Human_SNP_ID_311596744 A-to-I Human chr7 - 16089217 16089217 16089217 ATATATGTATATACGTACGCATACACACATATATGTATATACGTACGTATATACACACATATATG ATATATGTATATACGTACGCATACACACATATGTGTATATACGTACGTATATACACACATATATG T C CRPPA Ensembl:ENSG00000214960 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1408226815 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112717,RMVar_hsa_circ_116458,RMVar_hsa_circ_243875,RMVar_hsa_circ_243876 32609 RMVar_ID_32609 Human_SNP_ID_311596748 A-to-I Human chr7 - 16089221 16089220 16089222 ACACATATATGTATATACGTACGCATACACACATATATGTATATACGTACGTATATACACACATA ACACATATATGTATATACGTACGCATACACA__TATATGTATATACGTACGTATATACACACATA ATG A CRPPA Ensembl:ENSG00000214960 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1354273700 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_112717,RMVar_hsa_circ_116458,RMVar_hsa_circ_243875,RMVar_hsa_circ_243876 32610 RMVar_ID_32610 Human_SNP_ID_311596756 A-to-I Human chr7 - 16089233 16089233 16089233 ACGTACGCATACACACATATATGTATATACGTACGCATACACACATATATGTATATACGTACGTA ACGTACGCATACACACATATATGTATATACGTGCGCATACACACATATATGTATATACGTACGTA T C CRPPA Ensembl:ENSG00000214960 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs760402041 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112717,RMVar_hsa_circ_116458,RMVar_hsa_circ_243875,RMVar_hsa_circ_243876 32611 RMVar_ID_32611 Human_SNP_ID_311596789 A-to-I Human chr7 - 16089269 16089269 16089269 ATGTATATACGTACGCATACACACATATATGTATATACGTACGCATACACACATATATGTATATA ATGTATATACGTACGCATACACACATATATGTGTATACGTACGCATACACACATATATGTATATA T C CRPPA Ensembl:ENSG00000214960 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1424098564 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112717,RMVar_hsa_circ_116458,RMVar_hsa_circ_243875,RMVar_hsa_circ_243876 32612 RMVar_ID_32612 Human_SNP_ID_311596796 A-to-I Human chr7 - 16089273 16089273 16089273 ATATATGTATATACGTACGCATACACACATATATGTATATACGTACGCATACACACATATATGTA ATATATGTATATACGTACGCATACACACATATGTGTATATACGTACGCATACACACATATATGTA T C CRPPA Ensembl:ENSG00000214960 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1197082860 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112717,RMVar_hsa_circ_116458,RMVar_hsa_circ_243875,RMVar_hsa_circ_243876 32613 RMVar_ID_32613 Human_SNP_ID_311596813 A-to-I Human chr7 - 16089301 16089299 16089301 ATATATTTATATACGTACGCATACACACATATATGTATATACGTACGCATACACACATATATGTA ATATATTTATATACGTACGCATACACACATAT__GTATATACGTACGCATACACACATATATGTA CAT C CRPPA Ensembl:ENSG00000214960 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs773538068 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_112717,RMVar_hsa_circ_116458,RMVar_hsa_circ_243875,RMVar_hsa_circ_243876 32614 RMVar_ID_32614 Human_SNP_ID_311596822 A-to-I Human chr7 - 16089303 16089303 16089303 ACATATATTTATATACGTACGCATACACACATATATGTATATACGTACGCATACACACATATATG ACATATATTTATATACGTACGCATACACACATGTATGTATATACGTACGCATACACACATATATG T C CRPPA Ensembl:ENSG00000214960 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1453367385 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112717,RMVar_hsa_circ_116458,RMVar_hsa_circ_243875,RMVar_hsa_circ_243876 32615 RMVar_ID_32615 Human_SNP_ID_311596833 A-to-I Human chr7 - 16089309 16089309 16089309 ATACACACATATATTTATATACGTACGCATACACACATATATGTATATACGTACGCATACACACA ATACACACATATATTTATATACGTACGCATACCCACATATATGTATATACGTACGCATACACACA T G CRPPA Ensembl:ENSG00000214960 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1294095544 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112717,RMVar_hsa_circ_116458,RMVar_hsa_circ_243875,RMVar_hsa_circ_243876 32616 RMVar_ID_32616 Human_SNP_ID_311596849 A-to-I Human chr7 - 16089325 16089323 16089326 ATGTATATACGTACGCATACACACATATATTTATATACGTACGCATACACACATATATGTATATA ATGTATATACGTACGCATACACACATATATT___ATACGTACGCATACACACATATATGTATATA TATA T CRPPA Ensembl:ENSG00000214960 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs954305229 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_112717,RMVar_hsa_circ_116458,RMVar_hsa_circ_243875,RMVar_hsa_circ_243876 32617 RMVar_ID_32617 Human_SNP_ID_311596856 A-to-I Human chr7 - 16089331 16089327 16089331 GTATGTATGTATATACGTACGCATACACACATATATTTATATACGTACGCATACACACATATATG GTATGTATGTATATACGTACGCATACACACAT____TTATATACGTACGCATACACACATATATG AATAT A CRPPA Ensembl:ENSG00000214960 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs757671702 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_112717,RMVar_hsa_circ_116458,RMVar_hsa_circ_243875,RMVar_hsa_circ_243876 32618 RMVar_ID_32618 Human_SNP_ID_311596857 A-to-I Human chr7 - 16089331 16089327 16089331 GTATGTATGTATATACGTACGCATACACACATATATTTATATACGTACGCATACACACATATATG GTATGTATGTATATACGTACGCATACACACAT__ATTTATATACGTACGCATACACACATATATG AATAT AAT CRPPA Ensembl:ENSG00000214960 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs757671702 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_112717,RMVar_hsa_circ_116458,RMVar_hsa_circ_243875,RMVar_hsa_circ_243876 32619 RMVar_ID_32619 Human_SNP_ID_311596858 A-to-I Human chr7 - 16089329 16089329 16089329 ATGTATGTATATACGTACGCATACACACATATATTTATATACGTACGCATACACACATATATGTA ATGTATGTATATACGTACGCATACACACATATGTTTATATACGTACGCATACACACATATATGTA T C CRPPA Ensembl:ENSG00000214960 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs989995835 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112717,RMVar_hsa_circ_116458,RMVar_hsa_circ_243875,RMVar_hsa_circ_243876 32620 RMVar_ID_32620 Human_SNP_ID_311596860 A-to-I Human chr7 - 16089331 16089331 16089331 GTATGTATGTATATACGTACGCATACACACATATATTTATATACGTACGCATACACACATATATG GTATGTATGTATATACGTACGCATACACACATGTATTTATATACGTACGCATACACACATATATG T C CRPPA Ensembl:ENSG00000214960 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1417308931 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112717,RMVar_hsa_circ_116458,RMVar_hsa_circ_243875,RMVar_hsa_circ_243876 32621 RMVar_ID_32621 Human_SNP_ID_311596881 A-to-I Human chr7 - 16089357 16089357 16089357 ATATATACGTATATATGTACATGCATGTATGTATGTATATACGTACGCATACACACATATATTTA ATATATACGTATATATGTACATGCATGTATGTGTGTATATACGTACGCATACACACATATATTTA T C CRPPA Ensembl:ENSG00000214960 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1250154694 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112717,RMVar_hsa_circ_116458,RMVar_hsa_circ_243875,RMVar_hsa_circ_243876 32622 RMVar_ID_32622 Human_SNP_ID_311596919 A-to-I Human chr7 - 16089383 16089383 16089383 TACATATATACACATTATGTACATACATATATACGTATATATGTACATGCATGTATGTATGTATA TACATATATACACATTATGTACATACATATATTCGTATATATGTACATGCATGTATGTATGTATA T A CRPPA Ensembl:ENSG00000214960 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1280391284 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112717,RMVar_hsa_circ_116458,RMVar_hsa_circ_243875,RMVar_hsa_circ_243876 32623 RMVar_ID_32623 Human_SNP_ID_311596924 A-to-I Human chr7 - 16089391 16089391 16089391 TATGTACGTACATATATACACATTATGTACATACATATATACGTATATATGTACATGCATGTATG TATGTACGTACATATATACACATTATGTACATGCATATATACGTATATATGTACATGCATGTATG T C CRPPA Ensembl:ENSG00000214960 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs547400634 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_106 RMVar_hsa_circ_112717,RMVar_hsa_circ_116458,RMVar_hsa_circ_243875,RMVar_hsa_circ_243876 32624 RMVar_ID_32624 Human_SNP_ID_311596958 A-to-I Human chr7 - 16089446 16089419 16089447 ATGTACGTACATATATACACATATATGTATGCACGTACATATATACACATATATGTATGTACGTA ATGTACGTACATATATACACATATATGTATG____________________________TACGTA ACATACATATATGTGTATATATGTACGTG A CRPPA Ensembl:ENSG00000214960 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1380211699 Functional Loss DEL dbSNP153 32..59 33 - - - Human_RBP_ID_17578351 RMVar_hsa_circ_112717,RMVar_hsa_circ_116458,RMVar_hsa_circ_243875,RMVar_hsa_circ_243876 32625 RMVar_ID_32625 Human_SNP_ID_311596976 A-to-I Human chr7 - 16089432 16089432 16089432 ATACACATATATGTATGCACGTACATATATACACATATATGTATGTACGTACATATATACACATT ATACACATATATGTATGCACGTACATATATACGCATATATGTATGTACGTACATATATACACATT T C CRPPA Ensembl:ENSG00000214960 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs930725908 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17578351 RMVar_hsa_circ_112717,RMVar_hsa_circ_116458,RMVar_hsa_circ_243875,RMVar_hsa_circ_243876 32626 RMVar_ID_32626 Human_SNP_ID_311596977 A-to-I Human chr7 - 16089432 16089432 16089432 ATACACATATATGTATGCACGTACATATATACACATATATGTATGTACGTACATATATACACATT ATACACATATATGTATGCACGTACATATATACCCATATATGTATGTACGTACATATATACACATT T G CRPPA Ensembl:ENSG00000214960 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs930725908 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17578351 RMVar_hsa_circ_112717,RMVar_hsa_circ_116458,RMVar_hsa_circ_243875,RMVar_hsa_circ_243876 32627 RMVar_ID_32627 Human_SNP_ID_311597398 A-to-I Human chr7 - 16090447 16090447 16090447 TGCCTGCCTCGGCCTCCCAAAATGCTGGGATTATAGGTGTGAGCCACCATACCCAGCCAACATAC TGCCTGCCTCGGCCTCCCAAAATGCTGGGATTGTAGGTGTGAGCCACCATACCCAGCCAACATAC T C CRPPA Ensembl:ENSG00000214960 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1295279819 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112717,RMVar_hsa_circ_116458,RMVar_hsa_circ_243875,RMVar_hsa_circ_243876 32628 RMVar_ID_32628 Human_SNP_ID_311597402 A-to-I Human chr7 - 16090458 16090458 16090458 CTCAAGTGATCTGCCTGCCTCGGCCTCCCAAAATGCTGGGATTATAGGTGTGAGCCACCATACCC CTCAAGTGATCTGCCTGCCTCGGCCTCCCAAATTGCTGGGATTATAGGTGTGAGCCACCATACCC T A CRPPA Ensembl:ENSG00000214960 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348836439 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112717,RMVar_hsa_circ_116458,RMVar_hsa_circ_243875,RMVar_hsa_circ_243876 32629 RMVar_ID_32629 Human_SNP_ID_311730576 A-to-I Human chr7 + 16584414 16584414 16584414 TGAAGCATGGGAGCAAACACCGGCTATGAGGGATAGTGGGCCATGGGCTGCATCATGGCAGGTGG TGAAGCATGGGAGCAAACACCGGCTATGAGGGGTAGTGGGCCATGGGCTGCATCATGGCAGGTGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251041940 Functional Loss SNV dbSNP153 33..33 33 - - - 32630 RMVar_ID_32630 Human_SNP_ID_311731037 A-to-I Human chr7 - 16586084 16586084 16586084 ACAGCAACAGCGACAACTACGACCTCGAGTCCAACATGTCCAATGGATGGGACCCCAATGAAATG ACAGCAACAGCGACAACTACGACCTCGAGTCCGACATGTCCAATGGATGGGACCCCAATGAAATG T C AC005014.1 Ensembl:ENSG00000224280 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1177551692 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3868311,Human_RBP_ID_4934438,Human_RBP_ID_5105344,Human_RBP_ID_7779905 32631 RMVar_ID_32631 Human_SNP_ID_311731048 A-to-I Human chr7 - 16586102 16586102 16586102 AGCGCTGGGAGCGGGGTGACAGCAACAGCGACAACTACGACCTCGAGTCCAACATGTCCAATGGA AGCGCTGGGAGCGGGGTGACAGCAACAGCGACGACTACGACCTCGAGTCCAACATGTCCAATGGA T C AC005014.1 Ensembl:ENSG00000224280 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264954766 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7779905 32632 RMVar_ID_32632 Human_SNP_ID_311736404 A-to-I Human chr7 - 16606247 16606247 16606247 TTTGTATTTTCAGTAGAGTCGGGGCTTCACCAAGTTGGTCAGGCTGCTCTCAAACTCCTAACCTC TTTGTATTTTCAGTAGAGTCGGGGCTTCACCAGGTTGGTCAGGCTGCTCTCAAACTCCTAACCTC T C ANKMY2 Ensembl:ENSG00000106524 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs977032901 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32257,RMVar_hsa_circ_243893,RMVar_hsa_circ_10078,RMVar_hsa_circ_243895,RMVar_hsa_circ_307582,RMVar_hsa_circ_316176,RMVar_hsa_circ_243896,RMVar_hsa_circ_243894 32633 RMVar_ID_32633 Human_SNP_ID_311745613 A-to-I Human chr7 - 16641171 16641171 16641171 GGAATGCAATGGTGCGCTCTCGGCTCACTGCAACCTCTGCCTCCCAAGTTCAAGCAATTCTCCTG GGAATGCAATGGTGCGCTCTCGGCTCACTGCATCCTCTGCCTCCCAAGTTCAAGCAATTCTCCTG T A ANKMY2 Ensembl:ENSG00000106524 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878966557 Functional Loss SNV dbSNP153 33..33 33 - - - 32634 RMVar_ID_32634 Human_SNP_ID_311745614 A-to-I Human chr7 - 16641171 16641171 16641171 GGAATGCAATGGTGCGCTCTCGGCTCACTGCAACCTCTGCCTCCCAAGTTCAAGCAATTCTCCTG GGAATGCAATGGTGCGCTCTCGGCTCACTGCACCCTCTGCCTCCCAAGTTCAAGCAATTCTCCTG T G ANKMY2 Ensembl:ENSG00000106524 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878966557 Functional Loss SNV dbSNP153 33..33 33 - - - 32635 RMVar_ID_32635 Human_SNP_ID_311785038 A-to-I Human chr7 - 16783311 16783311 16783311 AAAATAACTTTGGACCCTCTCAATCGCTTTGCATCTTTTGTTCAACGGGGAGAGATTTTTTTTCT AAAATAACTTTGGACCCTCTCAATCGCTTTGCGTCTTTTGTTCAACGGGGAGAGATTTTTTTTCT T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1018559760 Functional Loss SNV dbSNP153 33..33 33 - - - 32636 RMVar_ID_32636 Human_SNP_ID_311815749 A-to-I Human chr7 + 16888752 16888752 16888752 AGGAAATTGTTGATACTCTTCTAGGATTTGATAACTTTGTCAATATGGTACTGCAAGATATCACT AGGAAATTGTTGATACTCTTCTAGGATTTGATGACTTTGTCAATATGGTACTGCAAGATATCACT A G AC098592.2 Ensembl:ENSG00000227965 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs751830700 Functional Loss SNV dbSNP153 33..33 33 - - - 32637 RMVar_ID_32637 Human_SNP_ID_311940070 A-to-I Human chr7 + 17344769 17344769 17344769 CTCTTGCCTCAGCCTCCCGAGTTGCTGGGATTACAGGCATGTGCCACCATGCCCAGCTAATTTTT CTCTTGCCTCAGCCTCCCGAGTTGCTGGGATTGCAGGCATGTGCCACCATGCCCAGCTAATTTTT A G AHR,AC019117.4 Ensembl:ENSG00000106546,Ensembl:ENSG00000283321 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1436837096 Functional Loss SNV dbSNP153 33..33 33 - - - 32638 RMVar_ID_32638 Human_SNP_ID_311940071 A-to-I Human chr7 + 17344769 17344769 17344769 CTCTTGCCTCAGCCTCCCGAGTTGCTGGGATTACAGGCATGTGCCACCATGCCCAGCTAATTTTT CTCTTGCCTCAGCCTCCCGAGTTGCTGGGATTTCAGGCATGTGCCACCATGCCCAGCTAATTTTT A T AHR,AC019117.4 Ensembl:ENSG00000106546,Ensembl:ENSG00000283321 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1436837096 Functional Loss SNV dbSNP153 33..33 33 - - - 32639 RMVar_ID_32639 Human_SNP_ID_311940075 A-to-I Human chr7 + 17344795 17344795 17344795 GGGATTACAGGCATGTGCCACCATGCCCAGCTAATTTTTGTATTTTTAGTAGAAACGGGTTTCAC GGGATTACAGGCATGTGCCACCATGCCCAGCTGATTTTTGTATTTTTAGTAGAAACGGGTTTCAC A G AHR,AC019117.4 Ensembl:ENSG00000106546,Ensembl:ENSG00000283321 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs35548334 Functional Loss SNV dbSNP153 33..33 33 - - - 32640 RMVar_ID_32640 Human_SNP_ID_311940076 A-to-I Human chr7 + 17344810 17344810 17344810 TGCCACCATGCCCAGCTAATTTTTGTATTTTTAGTAGAAACGGGTTTCACCATGTTGGCCAGACT TGCCACCATGCCCAGCTAATTTTTGTATTTTTGGTAGAAACGGGTTTCACCATGTTGGCCAGACT A G AHR,AC019117.4 Ensembl:ENSG00000106546,Ensembl:ENSG00000283321 Protein coding,Protein coding 3'UTR,intron GSE47997;GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831 K562 cells&HepG2 cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line - 23474544,29129909,32596459 RNA-Seq:(High) rs1213545483 Functional Loss SNV dbSNP153 33..33 33 - - - 32641 RMVar_ID_32641 Human_SNP_ID_311940078 A-to-I Human chr7 + 17344813 17344813 17344813 CACCATGCCCAGCTAATTTTTGTATTTTTAGTAGAAACGGGTTTCACCATGTTGGCCAGACTGGT CACCATGCCCAGCTAATTTTTGTATTTTTAGTGGAAACGGGTTTCACCATGTTGGCCAGACTGGT A G AHR,AC019117.4 Ensembl:ENSG00000106546,Ensembl:ENSG00000283321 Protein coding,Protein coding 3'UTR,intron GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs1339394106 Functional Loss SNV dbSNP153 33..33 33 - - - 32642 RMVar_ID_32642 Human_SNP_ID_311940079 A-to-I Human chr7 + 17344816 17344816 17344816 CATGCCCAGCTAATTTTTGTATTTTTAGTAGAAACGGGTTTCACCATGTTGGCCAGACTGGTCTC CATGCCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGTTTCACCATGTTGGCCAGACTGGTCTC A G AHR,AC019117.4 Ensembl:ENSG00000106546,Ensembl:ENSG00000283321 Protein coding,Protein coding 3'UTR,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1271866937 Functional Loss SNV dbSNP153 33..33 33 - - - 32643 RMVar_ID_32643 Human_SNP_ID_311940175 A-to-I Human chr7 + 17345150 17345150 17345150 CATCCTGACCAACATGGTGAAACCCTGTCTCTACTAAAAATACAGAAATTAGCTGGGCATGGTGG CATCCTGACCAACATGGTGAAACCCTGTCTCTGCTAAAAATACAGAAATTAGCTGGGCATGGTGG A G AHR,AC019117.4 Ensembl:ENSG00000106546,Ensembl:ENSG00000283321 Protein coding,Protein coding 3'UTR,intron GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,31158229,32596459 RNA-Seq:(High) rs1296937410 Functional Loss SNV dbSNP153 33..33 33 - - - 32644 RMVar_ID_32644 Human_SNP_ID_311940177 A-to-I Human chr7 + 17345153 17345153 17345153 CCTGACCAACATGGTGAAACCCTGTCTCTACTAAAAATACAGAAATTAGCTGGGCATGGTGGCGT CCTGACCAACATGGTGAAACCCTGTCTCTACTGAAAATACAGAAATTAGCTGGGCATGGTGGCGT A G AHR,AC019117.4 Ensembl:ENSG00000106546,Ensembl:ENSG00000283321 Protein coding,Protein coding 3'UTR,intron GSE47997;GSE38233;GSE38233;GSE99789;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490832,GSM3490833,GSM3490834;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;cultured B-cells;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,KYSE180 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,24183664,29796672,31158229,31158229,32596459,32596459 RNA-Seq:(High) rs530217400 Functional Loss SNV dbSNP153 33..33 33 - - - 32645 RMVar_ID_32645 Human_SNP_ID_311940178 A-to-I Human chr7 + 17345154 17345154 17345154 CTGACCAACATGGTGAAACCCTGTCTCTACTAAAAATACAGAAATTAGCTGGGCATGGTGGCGTG CTGACCAACATGGTGAAACCCTGTCTCTACTAGAAATACAGAAATTAGCTGGGCATGGTGGCGTG A G AHR,AC019117.4 Ensembl:ENSG00000106546,Ensembl:ENSG00000283321 Protein coding,Protein coding 3'UTR,intron GSE47997;GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,29129909,31158229,32596459 RNA-Seq:(High) rs1302968987 Functional Loss SNV dbSNP153 33..33 33 - - - 32646 RMVar_ID_32646 Human_SNP_ID_311940179 A-to-I Human chr7 + 17345155 17345155 17345155 TGACCAACATGGTGAAACCCTGTCTCTACTAAAAATACAGAAATTAGCTGGGCATGGTGGCGTGA TGACCAACATGGTGAAACCCTGTCTCTACTAAGAATACAGAAATTAGCTGGGCATGGTGGCGTGA A G AHR,AC019117.4 Ensembl:ENSG00000106546,Ensembl:ENSG00000283321 Protein coding,Protein coding 3'UTR,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1405912226 Functional Loss SNV dbSNP153 33..33 33 - - - 32647 RMVar_ID_32647 Human_SNP_ID_311940184 A-to-I Human chr7 + 17345159 17345159 17345159 CAACATGGTGAAACCCTGTCTCTACTAAAAATACAGAAATTAGCTGGGCATGGTGGCGTGAGCCT CAACATGGTGAAACCCTGTCTCTACTAAAAATGCAGAAATTAGCTGGGCATGGTGGCGTGAGCCT A G AHR,AC019117.4 Ensembl:ENSG00000106546,Ensembl:ENSG00000283321 Protein coding,Protein coding 3'UTR,intron GSE38233;GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,32596459 RNA-Seq:(High) rs1040505149 Functional Loss SNV dbSNP153 33..33 33 - - - 32648 RMVar_ID_32648 Human_SNP_ID_311940185 A-to-I Human chr7 + 17345161 17345161 17345161 ACATGGTGAAACCCTGTCTCTACTAAAAATACAGAAATTAGCTGGGCATGGTGGCGTGAGCCTGT ACATGGTGAAACCCTGTCTCTACTAAAAATACGGAAATTAGCTGGGCATGGTGGCGTGAGCCTGT A G AHR,AC019117.4 Ensembl:ENSG00000106546,Ensembl:ENSG00000283321 Protein coding,Protein coding 3'UTR,intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1253118885 Functional Loss SNV dbSNP153 33..33 33 - - - 32649 RMVar_ID_32649 Human_SNP_ID_311940187 A-to-I Human chr7 + 17345168 17345168 17345168 GAAACCCTGTCTCTACTAAAAATACAGAAATTAGCTGGGCATGGTGGCGTGAGCCTGTAGTCCTA GAAACCCTGTCTCTACTAAAAATACAGAAATTGGCTGGGCATGGTGGCGTGAGCCTGTAGTCCTA A G AHR,AC019117.4 Ensembl:ENSG00000106546,Ensembl:ENSG00000283321 Protein coding,Protein coding 3'UTR,intron GSE47997;GSE38233;GSE100210;GSE99789 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 23474544,24183664,29129909,29796672 RNA-Seq:(High) rs1430276953 Functional Loss SNV dbSNP153 33..33 33 - - - 32650 RMVar_ID_32650 Human_SNP_ID_311940198 A-to-I Human chr7 + 17345194 17345194 17345194 GAAATTAGCTGGGCATGGTGGCGTGAGCCTGTAGTCCTAGCTACTCAGGAGGCTGAGGCAGGAGA GAAATTAGCTGGGCATGGTGGCGTGAGCCTGTGGTCCTAGCTACTCAGGAGGCTGAGGCAGGAGA A G AHR,AC019117.4 Ensembl:ENSG00000106546,Ensembl:ENSG00000283321 Protein coding,Protein coding 3'UTR,intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,31158229,31158229,32596459 RNA-Seq:(High) rs1251925046 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23315305 32651 RMVar_ID_32651 Human_SNP_ID_311940202 A-to-I Human chr7 + 17345208 17345208 17345208 ATGGTGGCGTGAGCCTGTAGTCCTAGCTACTCAGGAGGCTGAGGCAGGAGAATAGCCTGAACCTG ATGGTGGCGTGAGCCTGTAGTCCTAGCTACTCGGGAGGCTGAGGCAGGAGAATAGCCTGAACCTG A G AHR,AC019117.4 Ensembl:ENSG00000106546,Ensembl:ENSG00000283321 Protein coding,Protein coding 3'UTR,intron GSE47997;GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 23474544,24183664,29129909,31158229,31158229 RNA-Seq:(High) rs1283192947 Functional Loss SNV dbSNP153 33..33 33 - - - 32652 RMVar_ID_32652 Human_SNP_ID_311940208 A-to-I Human chr7 + 17345229 17345229 17345229 CCTAGCTACTCAGGAGGCTGAGGCAGGAGAATAGCCTGAACCTGGGAATCGGAGGTTGCAGAGCC CCTAGCTACTCAGGAGGCTGAGGCAGGAGAATGGCCTGAACCTGGGAATCGGAGGTTGCAGAGCC A G AHR,AC019117.4 Ensembl:ENSG00000106546,Ensembl:ENSG00000283321 Protein coding,Protein coding 3'UTR,intron GSE100210;GSE107867 HepG2 cell line;ASD brains,temporal_cortex - 29129909,30559470 RNA-Seq:(High) rs752020902 Functional Loss SNV dbSNP153 33..33 33 - - - 32653 RMVar_ID_32653 Human_SNP_ID_311940217 A-to-I Human chr7 + 17345256 17345256 17345256 AGAATAGCCTGAACCTGGGAATCGGAGGTTGCAGAGCCAAGATCGCCCCACTGCACTCCAGCCTG AGAATAGCCTGAACCTGGGAATCGGAGGTTGCGGAGCCAAGATCGCCCCACTGCACTCCAGCCTG A G AHR,AC019117.4 Ensembl:ENSG00000106546,Ensembl:ENSG00000283321 Protein coding,Protein coding 3'UTR,intron GSE47997;GSE38233;GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,29129909,32596459,32596459 RNA-Seq:(High) rs1023351233 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7721125,Human_RBP_ID_23315725,Human_RBP_ID_27530368 Human_Splice_Rec_846258 32654 RMVar_ID_32654 Human_SNP_ID_311940218 A-to-I Human chr7 + 17345258 17345258 17345258 AATAGCCTGAACCTGGGAATCGGAGGTTGCAGAGCCAAGATCGCCCCACTGCACTCCAGCCTGGC AATAGCCTGAACCTGGGAATCGGAGGTTGCAGGGCCAAGATCGCCCCACTGCACTCCAGCCTGGC A G AHR,AC019117.4 Ensembl:ENSG00000106546,Ensembl:ENSG00000283321 Protein coding,Protein coding 3'UTR,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1135845 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7721125,Human_RBP_ID_27530368 Human_Splice_Rec_846258 32655 RMVar_ID_32655 Human_SNP_ID_311940219 A-to-I Human chr7 + 17345262 17345262 17345262 GCCTGAACCTGGGAATCGGAGGTTGCAGAGCCAAGATCGCCCCACTGCACTCCAGCCTGGCAATA GCCTGAACCTGGGAATCGGAGGTTGCAGAGCCGAGATCGCCCCACTGCACTCCAGCCTGGCAATA A G AHR,AC019117.4 Ensembl:ENSG00000106546,Ensembl:ENSG00000283321 Protein coding,Protein coding 3'UTR,intron GSE47997;GSE100210;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829 K562 cells&HepG2 cells;HepG2 cell line;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line - 23474544,29129909,29129909,29796672,31158229 RNA-Seq:(High) rs1465070967 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7721125,Human_RBP_ID_27530368 Human_Splice_Rec_846258 32656 RMVar_ID_32656 Human_SNP_ID_312277031 A-to-I Human chr7 + 18547442 18547442 18547442 TATTTTTAGTGGAGACGGGGTTTCACCATGTTAGCCAGGACAGTCTTGATCTCCTGACCTTGTGA TATTTTTAGTGGAGACGGGGTTTCACCATGTTGGCCAGGACAGTCTTGATCTCCTGACCTTGTGA A G HDAC9 Ensembl:ENSG00000048052 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1333446277 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66611,RMVar_hsa_circ_31990,RMVar_hsa_circ_314801,RMVar_hsa_circ_73184,RMVar_hsa_circ_354401,RMVar_hsa_circ_243974,RMVar_hsa_circ_325841 32657 RMVar_ID_32657 Human_SNP_ID_312510124 A-to-I Human chr7 + 19354888 19354888 19354888 GGTGCTACACACTACAAACAACCAGATCTTGTAAGAACTCACTGTCACGAGAACAGCAAAGGGGA GGTGCTACACACTACAAACAACCAGATCTTGTGAGAACTCACTGTCACGAGAACAGCAAAGGGGA A G AC007091.1 Ensembl:ENSG00000223838 lincRNA intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1178362904 Functional Loss SNV dbSNP153 33..33 33 - - - 32658 RMVar_ID_32658 Human_SNP_ID_312752570 A-to-I Human chr7 - 20137927 20137927 20137927 ACTGGTCTGGAACTCCTGACCTCAGGTCATCCACCTGCCTCGGCCTCCCAGAGTGCTAGGATTAC ACTGGTCTGGAACTCCTGACCTCAGGTCATCCGCCTGCCTCGGCCTCCCAGAGTGCTAGGATTAC T C AC005062.1,MACC1 Ensembl:ENSG00000243004,Ensembl:ENSG00000183742 lincRNA,Protein coding intron,3'UTR GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1048714913 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_244007,RMVar_hsa_circ_122249 32659 RMVar_ID_32659 Human_SNP_ID_312752591 A-to-I Human chr7 - 20138004 20138004 20138004 GGATTACAGGCATGCACCACCTTGTCCGGGTAATTTTTGTATTTTTAGTGGAGACAAGGTTTTAC GGATTACAGGCATGCACCACCTTGTCCGGGTAGTTTTTGTATTTTTAGTGGAGACAAGGTTTTAC T C AC005062.1,MACC1 Ensembl:ENSG00000243004,Ensembl:ENSG00000183742 lincRNA,Protein coding intron,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs890114742 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_244007,RMVar_hsa_circ_122249 32660 RMVar_ID_32660 Human_SNP_ID_312752630 A-to-I Human chr7 - 20138151 20138150 20138151 ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTGAGCCAGAGTCTGGCTCTGTTGCCCAGACTGGAG ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTG_GCCAGAGTCTGGCTCTGTTGCCCAGACTGGAG CT C AC005062.1,MACC1 Ensembl:ENSG00000243004,Ensembl:ENSG00000183742 lincRNA,Protein coding intron,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1167348691 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_8220956 RMVar_hsa_circ_244007,RMVar_hsa_circ_122249 32661 RMVar_ID_32661 Human_SNP_ID_312752873 A-to-I Human chr7 - 20138797 20138797 20138797 GTGGTGGCAGGCGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATGGCGTGAACCCG GTGGTGGCAGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCG T C AC005062.1,MACC1 Ensembl:ENSG00000243004,Ensembl:ENSG00000183742 lincRNA,Protein coding intron,3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs549205722 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_244007,RMVar_hsa_circ_122249 32662 RMVar_ID_32662 Human_SNP_ID_312752874 A-to-I Human chr7 - 20138797 20138797 20138797 GTGGTGGCAGGCGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATGGCGTGAACCCG GTGGTGGCAGGCGCCTGTAGTCCCAGCTACTCCGGAGGCTGAGGCAGGAGAATGGCGTGAACCCG T G AC005062.1,MACC1 Ensembl:ENSG00000243004,Ensembl:ENSG00000183742 lincRNA,Protein coding intron,3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs549205722 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_244007,RMVar_hsa_circ_122249 32663 RMVar_ID_32663 Human_SNP_ID_312752941 A-to-I Human chr7 - 20138914 20138914 20138914 AAATCCCAGCACTTTGGGAGGCCGAGGCGGGCAGATCACTAGGTCAGGAGATCGAGACCATCCTG AAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGGATCACTAGGTCAGGAGATCGAGACCATCCTG T C AC005062.1,MACC1 Ensembl:ENSG00000243004,Ensembl:ENSG00000183742 lincRNA,Protein coding intron,3'UTR GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1037073977 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2154364,Human_miRNA_ID_2226218 RMVar_hsa_circ_244007,RMVar_hsa_circ_122249 32664 RMVar_ID_32664 Human_SNP_ID_312978562 A-to-I Human chr7 + 20944838 20944838 20944838 GCCATCTCGGCTCACTGCAAGCTCCGCCTCCCAGGTTCATGCCATTCTCCCGCCCCAGCCTCCCG GCCATCTCGGCTCACTGCAAGCTCCGCCTCCCGGGTTCATGCCATTCTCCCGCCCCAGCCTCCCG A G LINC01162 Ensembl:ENSG00000232790 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs902436281 Functional Loss SNV dbSNP153 33..33 33 - - - 32665 RMVar_ID_32665 Human_SNP_ID_313052720 A-to-I Human chr7 - 21220962 21220962 21220962 AACCACTTCAAGGGCTGCAGTGACCTGACGGAATACACAAAGCAACACGGGATTCCCATCCCAGT AACCACTTCAAGGGCTGCAGTGACCTGACGGACTACACAAAGCAACACGGGATTCCCATCCCAGT T G ASS1P11 Ensembl:ENSG00000225308 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1374674824 Functional Loss SNV dbSNP153 33..33 33 - - - 32666 RMVar_ID_32666 Human_SNP_ID_313253181 A-to-I Human chr7 - 21888579 21888579 21888579 AGGCTGAGACAGGAGAATGACTTGAATCTGGAAGGTGGAGGTTGCAGTGAGCCGAGATCACACCA AGGCTGAGACAGGAGAATGACTTGAATCTGGAGGGTGGAGGTTGCAGTGAGCCGAGATCACACCA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170230998 Functional Loss SNV dbSNP153 33..33 33 - - - 32667 RMVar_ID_32667 Human_SNP_ID_313257686 A-to-I Human chr7 - 21901486 21901473 21901486 CGGCTCACTGCAACCTTTGCCTCCTAGGTTCAAGTGATTCTCCTACCTCCTGAGTAACTGGGATT CGGCTCACTGCAACCTTTGCCTCCTAGGTTCA_____________CCTCCTGAGTAACTGGGATT GTAGGAGAATCACT G CDCA7L Ensembl:ENSG00000164649 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1196688482 Functional Loss DEL dbSNP153 33..45 33 - - - Human_RBP_ID_2039555,Human_RBP_ID_24206684 32668 RMVar_ID_32668 Human_SNP_ID_313328833 A-to-I Human chr7 - 22160075 22160075 22160075 AGACATAGTCTCACTCTGCTGCTCAGCCTGGAATGCAGCAGCGCAATCTCGGCTCACTGCAACCT AGACATAGTCTCACTCTGCTGCTCAGCCTGGACTGCAGCAGCGCAATCTCGGCTCACTGCAACCT T G RAPGEF5 Ensembl:ENSG00000136237 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1353840451 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21490,RMVar_hsa_circ_30810,RMVar_hsa_circ_55791,RMVar_hsa_circ_355621,RMVar_hsa_circ_52295,RMVar_hsa_circ_55107,RMVar_hsa_circ_46296,RMVar_hsa_circ_244042,RMVar_hsa_circ_8395,RMVar_hsa_circ_244039,RMVar_hsa_circ_73799,RMVar_hsa_circ_339289,RMVar_hsa_circ_74249,RMVar_hsa_circ_321633,RMVar_hsa_circ_362783,RMVar_hsa_circ_314912,RMVar_hsa_circ_336066,RMVar_hsa_circ_355103,RMVar_hsa_circ_244043,RMVar_hsa_circ_244040,RMVar_hsa_circ_244041,RMVar_hsa_circ_65505,RMVar_hsa_circ_358059,RMVar_hsa_circ_365791,RMVar_hsa_circ_41237 32669 RMVar_ID_32669 Human_SNP_ID_313532982 A-to-I Human chr7 - 22989486 22989486 22989486 TAAATTAGCTGGGCGTGTTGGTGCATGCCTGTAGCCCCAGCTACTTGGGAGGCTGAGTTGGGAGG TAAATTAGCTGGGCGTGTTGGTGCATGCCTGTGGCCCCAGCTACTTGGGAGGCTGAGTTGGGAGG T C FAM126A Ensembl:ENSG00000122591 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1176952787 Functional Loss SNV dbSNP153 33..33 33 - - - 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 32670 RMVar_ID_32670 Human_SNP_ID_313584676 A-to-I Human chr7 + 23187706 23187706 23187706 TCGGCTCACTGTGACCTCTGCCTCCCAGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGC TCGGCTCACTGTGACCTCTGCCTCCCAGGTTCTAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGC A T NUP42 Ensembl:ENSG00000136243 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1343731919 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_244090,RMVar_hsa_circ_80945,RMVar_hsa_circ_288355,RMVar_hsa_circ_244091,RMVar_hsa_circ_244092,RMVar_hsa_circ_86631 32671 RMVar_ID_32671 Human_SNP_ID_313584696 A-to-I Human chr7 + 23187772 23187772 23187772 GGGATTACAGTTGCCCGCTACCACACCTGGCTAATTTTTGTATTTTTCTAGAGACGGGGTTTTAC GGGATTACAGTTGCCCGCTACCACACCTGGCTGATTTTTGTATTTTTCTAGAGACGGGGTTTTAC A G NUP42 Ensembl:ENSG00000136243 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs962826550 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16112924 RMVar_hsa_circ_244090,RMVar_hsa_circ_80945,RMVar_hsa_circ_288355,RMVar_hsa_circ_244091,RMVar_hsa_circ_244092,RMVar_hsa_circ_86631 32672 RMVar_ID_32672 Human_SNP_ID_313584716 A-to-I Human chr7 + 23187866 23187866 23187866 GACCTCAGGTGATCCGCCCGCCACAGGCTCCTAAAGTGCTGGGATTATAGGCGTGAGCCACCACA GACCTCAGGTGATCCGCCCGCCACAGGCTCCTGAAGTGCTGGGATTATAGGCGTGAGCCACCACA A G NUP42 Ensembl:ENSG00000136243 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1313259173 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_244090,RMVar_hsa_circ_80945,RMVar_hsa_circ_288355,RMVar_hsa_circ_244091,RMVar_hsa_circ_244092,RMVar_hsa_circ_86631 32673 RMVar_ID_32673 Human_SNP_ID_313584951 A-to-I Human chr7 + 23188565 23188565 23188565 GTGGATTCCTGAATATAGTTGTCAGATAAAATATGGGACATCCGGTTAAATTTAAATTTCAGATA GTGGATTCCTGAATATAGTTGTCAGATAAAATGTGGGACATCCGGTTAAATTTAAATTTCAGATA A G NUP42 Ensembl:ENSG00000136243 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs542167535 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_244090,RMVar_hsa_circ_80945,RMVar_hsa_circ_288355,RMVar_hsa_circ_244091,RMVar_hsa_circ_244092,RMVar_hsa_circ_86631 32674 RMVar_ID_32674 Human_SNP_ID_313585218 A-to-I Human chr7 + 23189730 23189730 23189730 GTCAGGAGATGGAGACCATCCTGGCTAACACGATGAAACCCCATCTCTACTAAAAAATACAAAAA GTCAGGAGATGGAGACCATCCTGGCTAACACGTTGAAACCCCATCTCTACTAAAAAATACAAAAA A T NUP42 Ensembl:ENSG00000136243 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1222709623 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_244090,RMVar_hsa_circ_80945,RMVar_hsa_circ_288355,RMVar_hsa_circ_244091,RMVar_hsa_circ_244092,RMVar_hsa_circ_86631 32675 RMVar_ID_32675 Human_SNP_ID_313585852 A-to-I Human chr7 + 23192467 23192467 23192467 TACTGTGGAGGCTGAGGCAGGAGAATTGCCTGAACCCAGGAGGCCGAGGTTGCAGTAAGCCGAGA TACTGTGGAGGCTGAGGCAGGAGAATTGCCTGCACCCAGGAGGCCGAGGTTGCAGTAAGCCGAGA A C NUP42 Ensembl:ENSG00000136243 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1269423781 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16113140 RMVar_hsa_circ_244090,RMVar_hsa_circ_80945,RMVar_hsa_circ_288355,RMVar_hsa_circ_244091,RMVar_hsa_circ_244092,RMVar_hsa_circ_86631 32676 RMVar_ID_32676 Human_SNP_ID_313586561 A-to-I Human chr7 + 23194426 23194426 23194426 TTGCCCAGGCTGGAGTGCAGTGGCGCCATCTCAGCTCACTACAGCCTCGGCTGGCCTTCCGGGTT TTGCCCAGGCTGGAGTGCAGTGGCGCCATCTCGGCTCACTACAGCCTCGGCTGGCCTTCCGGGTT A G NUP42 Ensembl:ENSG00000136243 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1195243660 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16113156,Human_RBP_ID_18880374 RMVar_hsa_circ_244090,RMVar_hsa_circ_80945,RMVar_hsa_circ_288355,RMVar_hsa_circ_244091,RMVar_hsa_circ_244092,RMVar_hsa_circ_86631 32677 RMVar_ID_32677 Human_SNP_ID_313588182 A-to-I Human chr7 + 23200460 23200460 23200460 CTTCCAGCTTCCTTGGCAACAGGTCCTGTCAGAGCTCCAGTGGCCCCAGCCTTTGGAGGTGGCAG CTTCCAGCTTCCTTGGCAACAGGTCCTGTCAGCGCTCCAGTGGCCCCAGCCTTTGGAGGTGGCAG A C NUP42 Ensembl:ENSG00000136243 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs747435974 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16113268,Human_RBP_ID_18880383,Human_RBP_ID_22110681 32678 RMVar_ID_32678 Human_SNP_ID_313614884 A-to-I Human chr7 + 23301527 23301527 23301527 GGGATCCGCCTGCCTCAGCCTCCTAAAGTGCTAGGATTACTGGCATGAGCCACCTCACCCGGCCG GGGATCCGCCTGCCTCAGCCTCCTAAAGTGCTGGGATTACTGGCATGAGCCACCTCACCCGGCCG A G MALSU1 Ensembl:ENSG00000156928 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1363454155 Functional Loss SNV dbSNP153 33..33 33 - - - 32679 RMVar_ID_32679 Human_SNP_ID_313615312 A-to-I Human chr7 + 23302916 23302904 23302916 CTCCGGCCTAAGCCTCCTGAGTAGGTGGGATTATAGGCACCCACCACCACGCTTGGCTGATTTTT CTCCGGCCTAAGCCTCCTGAG____________TAGGCACCCACCACCACGCTTGGCTGATTTTT GTAGGTGGGATTA G MALSU1 Ensembl:ENSG00000156928 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1443747843 Functional Loss DEL dbSNP153 22..33 33 - - - 32680 RMVar_ID_32680 Human_SNP_ID_313615604 A-to-I Human chr7 + 23303844 23303844 23303844 AGAAAAAAAAAAAAAAAAAAGGCTGGGTTCACACTTGTAATCCCAGCACTTTGGGAGGCCAAGGC AGAAAAAAAAAAAAAAAAAAGGCTGGGTTCACGCTTGTAATCCCAGCACTTTGGGAGGCCAAGGC A G MALSU1 Ensembl:ENSG00000156928 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1010083238 Functional Loss SNV dbSNP153 33..33 33 - - - 32681 RMVar_ID_32681 Human_SNP_ID_313615776 A-to-I Human chr7 + 23304600 23304600 23304600 TAGCTCACTGCAGCCTGGAACTTCTGGGCTCGAGTGATCCTCTCACCTCAGCCTCCCAAGTTGCT TAGCTCACTGCAGCCTGGAACTTCTGGGCTCGCGTGATCCTCTCACCTCAGCCTCCCAAGTTGCT A C MALSU1 Ensembl:ENSG00000156928 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs555827916 Functional Loss SNV dbSNP153 33..33 33 - - - 32682 RMVar_ID_32682 Human_SNP_ID_313615785 A-to-I Human chr7 + 23304617 23304617 23304617 GAACTTCTGGGCTCGAGTGATCCTCTCACCTCAGCCTCCCAAGTTGCTAGGACTAGAGGAGTAGG GAACTTCTGGGCTCGAGTGATCCTCTCACCTCCGCCTCCCAAGTTGCTAGGACTAGAGGAGTAGG A C MALSU1 Ensembl:ENSG00000156928 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1354730907 Functional Loss SNV dbSNP153 33..33 33 - - - 32683 RMVar_ID_32683 Human_SNP_ID_313616128 A-to-I Human chr7 + 23305966 23305966 23305966 TCTGTAATCCTAGCACTTTGGGAGGCCGAGGCAGGCAGATCACCTGAGATCGGGAGTTCAAGACC TCTGTAATCCTAGCACTTTGGGAGGCCGAGGCGGGCAGATCACCTGAGATCGGGAGTTCAAGACC A G MALSU1 Ensembl:ENSG00000156928 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1168406702 Functional Loss SNV dbSNP153 33..33 33 - - - 32684 RMVar_ID_32684 Human_SNP_ID_313616146 A-to-I Human chr7 + 23306011 23306011 23306011 GAGATCGGGAGTTCAAGACCAGCCGCACCAACATGGAGAAACCCCGTCTCTACTGAAAATACAAA GAGATCGGGAGTTCAAGACCAGCCGCACCAACCTGGAGAAACCCCGTCTCTACTGAAAATACAAA A C MALSU1 Ensembl:ENSG00000156928 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388678483 Functional Loss SNV dbSNP153 33..33 33 - - - 32685 RMVar_ID_32685 Human_SNP_ID_313616147 A-to-I Human chr7 + 23306011 23306011 23306011 GAGATCGGGAGTTCAAGACCAGCCGCACCAACATGGAGAAACCCCGTCTCTACTGAAAATACAAA GAGATCGGGAGTTCAAGACCAGCCGCACCAACGTGGAGAAACCCCGTCTCTACTGAAAATACAAA A G MALSU1 Ensembl:ENSG00000156928 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388678483 Functional Loss SNV dbSNP153 33..33 33 - - - 32686 RMVar_ID_32686 Human_SNP_ID_313616173 A-to-I Human chr7 + 23306083 23306083 23306083 GGGCGTGGTGGCGCATGCCTGTAATCCCGGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAA GGGCGTGGTGGCGCATGCCTGTAATCCCGGCTGCTTGGGAGGCTGAGGCAGGAGAATCGCTTGAA A G MALSU1 Ensembl:ENSG00000156928 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1402336180 Functional Loss SNV dbSNP153 33..33 33 - - - 32687 RMVar_ID_32687 Human_SNP_ID_313631028 A-to-I Human chr7 - 23355748 23355748 23355748 TTGTACTTTTAGTAGAGACAGAGTTTTGTCATATTGTCCAAGCTGGTCTTGAACTCCTGACCTCA TTGTACTTTTAGTAGAGACAGAGTTTTGTCATGTTGTCCAAGCTGGTCTTGAACTCCTGACCTCA T C IGF2BP3 Ensembl:ENSG00000136231 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1366636902 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16114154 RMVar_hsa_circ_108136,RMVar_hsa_circ_244097,RMVar_hsa_circ_35933,RMVar_hsa_circ_55845,RMVar_hsa_circ_244106,RMVar_hsa_circ_113358,RMVar_hsa_circ_290108,RMVar_hsa_circ_244110,RMVar_hsa_circ_276694,RMVar_hsa_circ_112561,RMVar_hsa_circ_244112,RMVar_hsa_circ_369430,RMVar_hsa_circ_271728,RMVar_hsa_circ_122350,RMVar_hsa_circ_244115,RMVar_hsa_circ_244113,RMVar_hsa_circ_244114,RMVar_hsa_circ_378753,RMVar_hsa_circ_309326,RMVar_hsa_circ_340620,RMVar_hsa_circ_244123,RMVar_hsa_circ_14733 32688 RMVar_ID_32688 Human_SNP_ID_313631036 A-to-I Human chr7 - 23355770 23355770 23355770 CGCCACCATGCCTGGCTAATTTTTGTACTTTTAGTAGAGACAGAGTTTTGTCATATTGTCCAAGC CGCCACCATGCCTGGCTAATTTTTGTACTTTTCGTAGAGACAGAGTTTTGTCATATTGTCCAAGC T G IGF2BP3 Ensembl:ENSG00000136231 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1289578107 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108136,RMVar_hsa_circ_244097,RMVar_hsa_circ_35933,RMVar_hsa_circ_55845,RMVar_hsa_circ_244106,RMVar_hsa_circ_113358,RMVar_hsa_circ_290108,RMVar_hsa_circ_244110,RMVar_hsa_circ_276694,RMVar_hsa_circ_112561,RMVar_hsa_circ_244112,RMVar_hsa_circ_369430,RMVar_hsa_circ_271728,RMVar_hsa_circ_122350,RMVar_hsa_circ_244115,RMVar_hsa_circ_244113,RMVar_hsa_circ_244114,RMVar_hsa_circ_378753,RMVar_hsa_circ_309326,RMVar_hsa_circ_340620,RMVar_hsa_circ_244123,RMVar_hsa_circ_14733 32689 RMVar_ID_32689 Human_SNP_ID_313631064 A-to-I Human chr7 - 23355886 23355886 23355886 TTTCATCACCTAGGCTGGGGTGCAGTGGGGCAATCTTGGCTCACTGCAACCTCCGCCTCCCAGAT TTTCATCACCTAGGCTGGGGTGCAGTGGGGCAGTCTTGGCTCACTGCAACCTCCGCCTCCCAGAT T C IGF2BP3 Ensembl:ENSG00000136231 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1441904503 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16114156 RMVar_hsa_circ_108136,RMVar_hsa_circ_244097,RMVar_hsa_circ_35933,RMVar_hsa_circ_55845,RMVar_hsa_circ_244106,RMVar_hsa_circ_113358,RMVar_hsa_circ_290108,RMVar_hsa_circ_244110,RMVar_hsa_circ_276694,RMVar_hsa_circ_112561,RMVar_hsa_circ_244112,RMVar_hsa_circ_369430,RMVar_hsa_circ_271728,RMVar_hsa_circ_122350,RMVar_hsa_circ_244115,RMVar_hsa_circ_244113,RMVar_hsa_circ_244114,RMVar_hsa_circ_378753,RMVar_hsa_circ_309326,RMVar_hsa_circ_340620,RMVar_hsa_circ_244123,RMVar_hsa_circ_14733 32690 RMVar_ID_32690 Human_SNP_ID_313631165 A-to-I Human chr7 - 23356307 23356307 23356307 GTGATCCTCCCTCCTTGGCCTCCCAGAGTGCTAGAATTAGAGGTGTGAGCTCCTGCACCCAGCCA GTGATCCTCCCTCCTTGGCCTCCCAGAGTGCTCGAATTAGAGGTGTGAGCTCCTGCACCCAGCCA T G IGF2BP3 Ensembl:ENSG00000136231 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1010689384 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108136,RMVar_hsa_circ_244097,RMVar_hsa_circ_35933,RMVar_hsa_circ_55845,RMVar_hsa_circ_244106,RMVar_hsa_circ_113358,RMVar_hsa_circ_290108,RMVar_hsa_circ_244110,RMVar_hsa_circ_276694,RMVar_hsa_circ_112561,RMVar_hsa_circ_244112,RMVar_hsa_circ_369430,RMVar_hsa_circ_271728,RMVar_hsa_circ_122350,RMVar_hsa_circ_244115,RMVar_hsa_circ_244113,RMVar_hsa_circ_244114,RMVar_hsa_circ_378753,RMVar_hsa_circ_309326,RMVar_hsa_circ_340620,RMVar_hsa_circ_244123,RMVar_hsa_circ_14733 32691 RMVar_ID_32691 Human_SNP_ID_313634102 A-to-I Human chr7 - 23367220 23367220 23367220 TAATCCCAGCATTTGGGAAGGCTGAGGCAGGCAGATCACTTGAGCTCAGGAATTCGGGACTAGCC TAATCCCAGCATTTGGGAAGGCTGAGGCAGGCTGATCACTTGAGCTCAGGAATTCGGGACTAGCC T A IGF2BP3 Ensembl:ENSG00000136231 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs751775038 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16114411 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_32420,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 32692 RMVar_ID_32692 Human_SNP_ID_313634103 A-to-I Human chr7 - 23367220 23367220 23367220 TAATCCCAGCATTTGGGAAGGCTGAGGCAGGCAGATCACTTGAGCTCAGGAATTCGGGACTAGCC TAATCCCAGCATTTGGGAAGGCTGAGGCAGGCCGATCACTTGAGCTCAGGAATTCGGGACTAGCC T G IGF2BP3 Ensembl:ENSG00000136231 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs751775038 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16114411 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_32420,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 32693 RMVar_ID_32693 Human_SNP_ID_313636320 A-to-I Human chr7 - 23374493 23374493 23374493 ATTTTTATTTTTGTAGAGATGGGGTCTTTCCTATGTTGCCCAGGCTGGTCTCAAACTCTTGGCCT ATTTTTATTTTTGTAGAGATGGGGTCTTTCCTGTGTTGCCCAGGCTGGTCTCAAACTCTTGGCCT T C IGF2BP3 Ensembl:ENSG00000136231 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs374475446 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16114605 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_32420,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 32694 RMVar_ID_32694 Human_SNP_ID_313636876 A-to-I Human chr7 - 23376504 23376504 23376504 GGGAGATGGAGCCTTACTCTGTTGCCCAGGCTAAAGTGCAGTGGTGTGATCTTGGCTCACTGCAA GGGAGATGGAGCCTTACTCTGTTGCCCAGGCTGAAGTGCAGTGGTGTGATCTTGGCTCACTGCAA T C IGF2BP3 Ensembl:ENSG00000136231 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1206450726 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16114660,Human_RBP_ID_26093133 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_32420,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 32695 RMVar_ID_32695 Human_SNP_ID_313639909 A-to-I Human chr7 - 23386939 23386939 23386939 CCTCAGCCTCCCCAGTAGCTGGGATTACAGGTACTTGCCACCATGCCTGTTTAATTTTTGTATTT CCTCAGCCTCCCCAGTAGCTGGGATTACAGGTGCTTGCCACCATGCCTGTTTAATTTTTGTATTT T C IGF2BP3 Ensembl:ENSG00000136231 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs370594805 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16114953 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_32420,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 32696 RMVar_ID_32696 Human_SNP_ID_313640868 A-to-I Human chr7 - 23389891 23389891 23389891 GCTCACTGCAGCCTTGACCTCCCAGTCTCCCAAGTAGCTGGGACTACAGATGCATACTACCACAC GCTCACTGCAGCCTTGACCTCCCAGTCTCCCAGGTAGCTGGGACTACAGATGCATACTACCACAC T C IGF2BP3 Ensembl:ENSG00000136231 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1008405952 Functional Loss SNV dbSNP153 33..33 33 - - - 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_32420,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 32697 RMVar_ID_32697 Human_SNP_ID_313644189 A-to-I Human chr7 - 23400842 23400842 23400842 TGGGCCAAGATCGTGCCTCTGCACTCCAGCCTAGGCCACAGAGCAAGGCTCCATCTCAGAAAAAT TGGGCCAAGATCGTGCCTCTGCACTCCAGCCTGGGCCACAGAGCAAGGCTCCATCTCAGAAAAAT T C IGF2BP3 Ensembl:ENSG00000136231 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334710293 Functional Loss SNV dbSNP153 33..33 33 - - - 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_32420,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 32698 RMVar_ID_32698 Human_SNP_ID_313644600 A-to-I Human chr7 - 23402070 23402070 23402070 TTCTTTCACCCAGGCTGGAGCGCAGTGGTGCAATCTCGGCTCACTGCAGCCTCTGCCTCCTGGGT TTCTTTCACCCAGGCTGGAGCGCAGTGGTGCAGTCTCGGCTCACTGCAGCCTCTGCCTCCTGGGT T C IGF2BP3 Ensembl:ENSG00000136231 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs543847877 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16115363 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_32420,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 32699 RMVar_ID_32699 Human_SNP_ID_313644651 A-to-I Human chr7 - 23402240 23402240 23402240 ATATGTTACTTTTGCTGATCACATACAGGTAAATCCATCTTAGATGATCTGATTTCTAATACAAC ATATGTTACTTTTGCTGATCACATACAGGTAAGTCCATCTTAGATGATCTGATTTCTAATACAAC T C IGF2BP3 Ensembl:ENSG00000136231 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs903232576 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17577719 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_32420,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 32700 RMVar_ID_32700 Human_SNP_ID_313645575 A-to-I Human chr7 - 23405650 23405650 23405650 GCAACCTAGATCCCTCGCGTGCGCAGTTCACAATAGGGTACGCACTTCCATGAGAATCTAACGCT GCAACCTAGATCCCTCGCGTGCGCAGTTCACAGTAGGGTACGCACTTCCATGAGAATCTAACGCT T C IGF2BP3 Ensembl:ENSG00000136231 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1461466723 Functional Loss SNV dbSNP153 33..33 33 - - - 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 32701 RMVar_ID_32701 Human_SNP_ID_313647348 A-to-I Human chr7 - 23411519 23411519 23411519 TGGAGTGCAGTGGCGTGATCTCTGCTCACTACAGTGTCCACCTCCTGGGTTCAAGCCATTCTCCG TGGAGTGCAGTGGCGTGATCTCTGCTCACTACGGTGTCCACCTCCTGGGTTCAAGCCATTCTCCG T C IGF2BP3 Ensembl:ENSG00000136231 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs868388645 Functional Loss SNV dbSNP153 33..33 33 - - - 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 32702 RMVar_ID_32702 Human_SNP_ID_313647508 A-to-I Human chr7 - 23412059 23412059 23412059 AAAATTGCTTGAGCCTAGGATGCAGAGGTTGCAGTGAGCTGAAATTGTGCCACTGTACTCCTGGG AAAATTGCTTGAGCCTAGGATGCAGAGGTTGCGGTGAGCTGAAATTGTGCCACTGTACTCCTGGG T C IGF2BP3 Ensembl:ENSG00000136231 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1386993650 Functional Loss SNV dbSNP153 33..33 33 - - - 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 32703 RMVar_ID_32703 Human_SNP_ID_313650014 A-to-I Human chr7 - 23421086 23421086 23421086 AGAATTGCCTGAACCCGGGAGGCAGAGGCTGCAGTGAGCTGAGATTGTGCCACTGAGTTCCAGCA AGAATTGCCTGAACCCGGGAGGCAGAGGCTGCTGTGAGCTGAGATTGTGCCACTGAGTTCCAGCA T A IGF2BP3 Ensembl:ENSG00000136231 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs373872198 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55845,RMVar_hsa_circ_122350,RMVar_hsa_circ_244113,RMVar_hsa_circ_108481,RMVar_hsa_circ_102538,RMVar_hsa_circ_267869,RMVar_hsa_circ_244126,RMVar_hsa_circ_244127,RMVar_hsa_circ_317425,RMVar_hsa_circ_244128 32704 RMVar_ID_32704 Human_SNP_ID_313651256 A-to-I Human chr7 - 23425532 23425532 23425532 CCATCTCTACAAAAAATTTAGCTGGGCATGGTAGCATATGCCTGTGGTCCCAGCTACTCAGAAGG CCATCTCTACAAAAAATTTAGCTGGGCATGGTGGCATATGCCTGTGGTCCCAGCTACTCAGAAGG T C IGF2BP3 Ensembl:ENSG00000136231 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1319196975 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55845,RMVar_hsa_circ_122350,RMVar_hsa_circ_244113,RMVar_hsa_circ_108481,RMVar_hsa_circ_102538,RMVar_hsa_circ_267869,RMVar_hsa_circ_244126,RMVar_hsa_circ_244127,RMVar_hsa_circ_317425,RMVar_hsa_circ_244128 32705 RMVar_ID_32705 Human_SNP_ID_313657564 A-to-I Human chr7 - 23447040 23447040 23447040 GCCACTGCACTTGACTAATTTTTTGTATTTTTAGTAGAGATGAGGTTTCACCATGTTGGGCAGGC GCCACTGCACTTGACTAATTTTTTGTATTTTTGGTAGAGATGAGGTTTCACCATGTTGGGCAGGC T C IGF2BP3 Ensembl:ENSG00000136231 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs945971038 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16116295 RMVar_hsa_circ_55845,RMVar_hsa_circ_122350,RMVar_hsa_circ_244113,RMVar_hsa_circ_108481,RMVar_hsa_circ_102538,RMVar_hsa_circ_267869,RMVar_hsa_circ_244126,RMVar_hsa_circ_244127,RMVar_hsa_circ_317425,RMVar_hsa_circ_244128 32706 RMVar_ID_32706 Human_SNP_ID_313657710 A-to-I Human chr7 - 23447495 23447495 23447495 TCAGCCTCCCGAGTAGCTGGGATTACAGGCACACACCCCATGCCTGGCTAATTTTTTTGTATTTT TCAGCCTCCCGAGTAGCTGGGATTACAGGCACGCACCCCATGCCTGGCTAATTTTTTTGTATTTT T C IGF2BP3 Ensembl:ENSG00000136231 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041493010 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55845,RMVar_hsa_circ_122350,RMVar_hsa_circ_244113,RMVar_hsa_circ_108481,RMVar_hsa_circ_102538,RMVar_hsa_circ_267869,RMVar_hsa_circ_244126,RMVar_hsa_circ_244127,RMVar_hsa_circ_317425,RMVar_hsa_circ_244128 32707 RMVar_ID_32707 Human_SNP_ID_313658219 A-to-I Human chr7 - 23449273 23449273 23449273 GACTTCGTGATCTGCCCGCCTCGGTCTCCCAAAGTGCTGGGATTTCAGGCATGAGCCACCACGCC GACTTCGTGATCTGCCCGCCTCGGTCTCCCAACGTGCTGGGATTTCAGGCATGAGCCACCACGCC T G IGF2BP3 Ensembl:ENSG00000136231 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1244832936 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22731128 RMVar_hsa_circ_55845,RMVar_hsa_circ_122350,RMVar_hsa_circ_244113,RMVar_hsa_circ_108481,RMVar_hsa_circ_102538,RMVar_hsa_circ_267869,RMVar_hsa_circ_244126,RMVar_hsa_circ_244127,RMVar_hsa_circ_317425,RMVar_hsa_circ_244128 32708 RMVar_ID_32708 Human_SNP_ID_313658293 A-to-I Human chr7 - 23449470 23449470 23449470 CGCTGTGTCCCAGGCTGGAGTGCAGTGGCGCTATCTCGGCTCACTGCAAGCTCTGCCTCCCGGTT CGCTGTGTCCCAGGCTGGAGTGCAGTGGCGCTTTCTCGGCTCACTGCAAGCTCTGCCTCCCGGTT T A IGF2BP3 Ensembl:ENSG00000136231 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs916459360 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16116355 RMVar_hsa_circ_55845,RMVar_hsa_circ_122350,RMVar_hsa_circ_244113,RMVar_hsa_circ_108481,RMVar_hsa_circ_102538,RMVar_hsa_circ_267869,RMVar_hsa_circ_244126,RMVar_hsa_circ_244127,RMVar_hsa_circ_317425,RMVar_hsa_circ_244128 32709 RMVar_ID_32709 Human_SNP_ID_313658294 A-to-I Human chr7 - 23449470 23449470 23449470 CGCTGTGTCCCAGGCTGGAGTGCAGTGGCGCTATCTCGGCTCACTGCAAGCTCTGCCTCCCGGTT CGCTGTGTCCCAGGCTGGAGTGCAGTGGCGCTGTCTCGGCTCACTGCAAGCTCTGCCTCCCGGTT T C IGF2BP3 Ensembl:ENSG00000136231 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs916459360 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16116355 RMVar_hsa_circ_55845,RMVar_hsa_circ_122350,RMVar_hsa_circ_244113,RMVar_hsa_circ_108481,RMVar_hsa_circ_102538,RMVar_hsa_circ_267869,RMVar_hsa_circ_244126,RMVar_hsa_circ_244127,RMVar_hsa_circ_317425,RMVar_hsa_circ_244128 32710 RMVar_ID_32710 Human_SNP_ID_313658991 A-to-I Human chr7 - 23451791 23451791 23451791 GGCGCCTGCCTCCATACTAGGCTAATTTTTGTATTTTCAGTAGGACAGGGTTTCACTACGTTGGC GGCGCCTGCCTCCATACTAGGCTAATTTTTGTGTTTTCAGTAGGACAGGGTTTCACTACGTTGGC T C IGF2BP3 Ensembl:ENSG00000136231 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1458889330 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3080802,Human_RBP_ID_16116421 RMVar_hsa_circ_55845,RMVar_hsa_circ_122350,RMVar_hsa_circ_244113,RMVar_hsa_circ_108481,RMVar_hsa_circ_102538,RMVar_hsa_circ_267869,RMVar_hsa_circ_244126,RMVar_hsa_circ_244127,RMVar_hsa_circ_317425,RMVar_hsa_circ_244128 32711 RMVar_ID_32711 Human_SNP_ID_313659006 A-to-I Human chr7 - 23451836 23451836 23451836 TCAAGTGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGAGATTATAGGCGCCTGCCTCCATACTAG TCAAGTGATTCTCCTGCCTCAGCCTCCTGAGTGGCTGAGATTATAGGCGCCTGCCTCCATACTAG T C IGF2BP3 Ensembl:ENSG00000136231 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs548521131 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55845,RMVar_hsa_circ_122350,RMVar_hsa_circ_244113,RMVar_hsa_circ_108481,RMVar_hsa_circ_102538,RMVar_hsa_circ_267869,RMVar_hsa_circ_244126,RMVar_hsa_circ_244127,RMVar_hsa_circ_317425,RMVar_hsa_circ_244128 32712 RMVar_ID_32712 Human_SNP_ID_313660112 A-to-I Human chr7 - 23455810 23455810 23455810 GTTGTGGCGGGCGCCTGTAGTCCCAGTTACTCAGGAGGCTGAGGCAGGAGAGTGGCTCGAATCCG GTTGTGGCGGGCGCCTGTAGTCCCAGTTACTCGGGAGGCTGAGGCAGGAGAGTGGCTCGAATCCG T C IGF2BP3 Ensembl:ENSG00000136231 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1562762772 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55845,RMVar_hsa_circ_122350,RMVar_hsa_circ_244113,RMVar_hsa_circ_108481,RMVar_hsa_circ_102538,RMVar_hsa_circ_267869,RMVar_hsa_circ_244126,RMVar_hsa_circ_244127,RMVar_hsa_circ_317425,RMVar_hsa_circ_244128 32713 RMVar_ID_32713 Human_SNP_ID_313676577 A-to-I Human chr7 - 23509686 23509686 23509686 GCTCTGTTGCCAGGCTGGAGGGCAGTGGCACAATCTCGGCTCACTGCAACCTCTGCCTCCCGGGT GCTCTGTTGCCAGGCTGGAGGGCAGTGGCACATTCTCGGCTCACTGCAACCTCTGCCTCCCGGGT T A TRA2A Ensembl:ENSG00000164548 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1347119482 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26093735 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 32714 RMVar_ID_32714 Human_SNP_ID_313676578 A-to-I Human chr7 - 23509686 23509686 23509686 GCTCTGTTGCCAGGCTGGAGGGCAGTGGCACAATCTCGGCTCACTGCAACCTCTGCCTCCCGGGT GCTCTGTTGCCAGGCTGGAGGGCAGTGGCACAGTCTCGGCTCACTGCAACCTCTGCCTCCCGGGT T C TRA2A Ensembl:ENSG00000164548 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1347119482 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26093735 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 32715 RMVar_ID_32715 Human_SNP_ID_313676579 A-to-I Human chr7 - 23509687 23509687 23509687 TGCTCTGTTGCCAGGCTGGAGGGCAGTGGCACAATCTCGGCTCACTGCAACCTCTGCCTCCCGGG TGCTCTGTTGCCAGGCTGGAGGGCAGTGGCACCATCTCGGCTCACTGCAACCTCTGCCTCCCGGG T G TRA2A Ensembl:ENSG00000164548 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1238485542 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26093735 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 32716 RMVar_ID_32716 Human_SNP_ID_313676625 A-to-I Human chr7 - 23509828 23509828 23509828 TAGAGACGGGGTTTTGCCCCATTGCCCAGGCTAGCCTCAAACTCTGGACCTCAAGTGATTTGGCC TAGAGACGGGGTTTTGCCCCATTGCCCAGGCTGGCCTCAAACTCTGGACCTCAAGTGATTTGGCC T C TRA2A Ensembl:ENSG00000164548 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992898278 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_792913,Human_RBP_ID_7724977,Human_RBP_ID_16117339 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 32717 RMVar_ID_32717 Human_SNP_ID_313676673 A-to-I Human chr7 - 23509974 23509974 23509974 TCGCCTAGGCTGGAGTGTGGTGGCACGATCTCAGCTCACTGCAACTTCCGCCTCCCAGGCTCAAG TCGCCTAGGCTGGAGTGTGGTGGCACGATCTCGGCTCACTGCAACTTCCGCCTCCCAGGCTCAAG T C TRA2A Ensembl:ENSG00000164548 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1193031284 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22834617,Human_RBP_ID_23197590 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 32718 RMVar_ID_32718 Human_SNP_ID_313676813 A-to-I Human chr7 - 23510398 23510398 23510398 TTGAACCTAGGAGGCGGAGGTTGCAGTGAGCTAAGTTTGTGCCACTTCACTCCAGCCTGGGCAAC TTGAACCTAGGAGGCGGAGGTTGCAGTGAGCTTAGTTTGTGCCACTTCACTCCAGCCTGGGCAAC T A TRA2A Ensembl:ENSG00000164548 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs935593102 Functional Loss SNV dbSNP153 33..33 33 - - - 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 32719 RMVar_ID_32719 Human_SNP_ID_313676840 A-to-I Human chr7 - 23510495 23510495 23510495 GGTGAAACCCCATCTGCTAAAATACAAAAATTAGCCGGGCATTGTGGCAAGCGCCTGTAACCCCA GGTGAAACCCCATCTGCTAAAATACAAAAATTGGCCGGGCATTGTGGCAAGCGCCTGTAACCCCA T C TRA2A Ensembl:ENSG00000164548 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs145521860 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16117367,Human_RBP_ID_26093749 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 32720 RMVar_ID_32720 Human_SNP_ID_313677514 A-to-I Human chr7 - 23512372 23512372 23512372 TCAAGCAGTCCTCCTACCTCAGCCTCCTGAGTAGCAGACACTACAAGTGTGGGCCACCATGCCCA TCAAGCAGTCCTCCTACCTCAGCCTCCTGAGTGGCAGACACTACAAGTGTGGGCCACCATGCCCA T C TRA2A Ensembl:ENSG00000164548 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1393881320 Functional Loss SNV dbSNP153 33..33 33 - - - 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 32721 RMVar_ID_32721 Human_SNP_ID_313677521 A-to-I Human chr7 - 23512389 23512389 23512389 GCCTCGACCTCCTGGGCTCAAGCAGTCCTCCTACCTCAGCCTCCTGAGTAGCAGACACTACAAGT GCCTCGACCTCCTGGGCTCAAGCAGTCCTCCTTCCTCAGCCTCCTGAGTAGCAGACACTACAAGT T A TRA2A Ensembl:ENSG00000164548 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs192106918 Functional Loss SNV dbSNP153 33..33 33 - - - 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 32722 RMVar_ID_32722 Human_SNP_ID_313677522 A-to-I Human chr7 - 23512389 23512389 23512389 GCCTCGACCTCCTGGGCTCAAGCAGTCCTCCTACCTCAGCCTCCTGAGTAGCAGACACTACAAGT GCCTCGACCTCCTGGGCTCAAGCAGTCCTCCTGCCTCAGCCTCCTGAGTAGCAGACACTACAAGT T C TRA2A Ensembl:ENSG00000164548 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs192106918 Functional Loss SNV dbSNP153 33..33 33 - - - 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 32723 RMVar_ID_32723 Human_SNP_ID_313677523 A-to-I Human chr7 - 23512389 23512389 23512389 GCCTCGACCTCCTGGGCTCAAGCAGTCCTCCTACCTCAGCCTCCTGAGTAGCAGACACTACAAGT GCCTCGACCTCCTGGGCTCAAGCAGTCCTCCTCCCTCAGCCTCCTGAGTAGCAGACACTACAAGT T G TRA2A Ensembl:ENSG00000164548 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs192106918 Functional Loss SNV dbSNP153 33..33 33 - - - 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 32724 RMVar_ID_32724 Human_SNP_ID_313677612 A-to-I Human chr7 - 23512626 23512622 23512626 GTGAAACCCCGTCTCTACTAAAAATACAAACAATTAGCCAGGCGTGGTGGCCGGCGCTTGTAGTC GTGAAACCCCGTCTCTACTAAAAATACAAACA____GCCAGGCGTGGTGGCCGGCGCTTGTAGTC CTAAT C TRA2A Ensembl:ENSG00000164548 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs903661532 Functional Loss DEL dbSNP153 33..36 33 - - - 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 32725 RMVar_ID_32725 Human_SNP_ID_313677615 A-to-I Human chr7 - 23512626 23512626 23512626 GTGAAACCCCGTCTCTACTAAAAATACAAACAATTAGCCAGGCGTGGTGGCCGGCGCTTGTAGTC GTGAAACCCCGTCTCTACTAAAAATACAAACAGTTAGCCAGGCGTGGTGGCCGGCGCTTGTAGTC T C TRA2A Ensembl:ENSG00000164548 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs930733350 Functional Loss SNV dbSNP153 33..33 33 - - - 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 32726 RMVar_ID_32726 Human_SNP_ID_313678656 A-to-I Human chr7 - 23516028 23516028 23516028 AGCTGGGGTTGCAGGTGTGCACCACCACACCCAGCTAATTTTTGTGTTTTTAGAAATGGGGTTTC AGCTGGGGTTGCAGGTGTGCACCACCACACCCGGCTAATTTTTGTGTTTTTAGAAATGGGGTTTC T C TRA2A Ensembl:ENSG00000164548 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1289444763 Functional Loss SNV dbSNP153 33..33 33 - - - 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_335045,RMVar_hsa_circ_361566,RMVar_hsa_circ_244134,RMVar_hsa_circ_281398,RMVar_hsa_circ_319385,RMVar_hsa_circ_244135 32727 RMVar_ID_32727 Human_SNP_ID_313678693 A-to-I Human chr7 - 23516138 23516138 23516138 AGAATGCAAAGGAAGTATATTTTCTTTTTTTTAGACAAAGTCTTACTCTGTCTCCCAGGCTGGAG AGAATGCAAAGGAAGTATATTTTCTTTTTTTTTGACAAAGTCTTACTCTGTCTCCCAGGCTGGAG T A TRA2A Ensembl:ENSG00000164548 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs868540814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16117461 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_335045,RMVar_hsa_circ_361566,RMVar_hsa_circ_244134,RMVar_hsa_circ_281398,RMVar_hsa_circ_319385,RMVar_hsa_circ_244135 32728 RMVar_ID_32728 Human_SNP_ID_313679286 A-to-I Human chr7 - 23517657 23517657 23517657 TGCCTGCCTCGGCCTCCCAAAGTACTGGGATTACAGGCATGAGCCACTGCGCCCAGCCTGATTTT TGCCTGCCTCGGCCTCCCAAAGTACTGGGATTGCAGGCATGAGCCACTGCGCCCAGCCTGATTTT T C TRA2A Ensembl:ENSG00000164548 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs563101114 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8969,RMVar_hsa_circ_69534,RMVar_hsa_circ_283918,RMVar_hsa_circ_355766,RMVar_hsa_circ_244132,RMVar_hsa_circ_361566,RMVar_hsa_circ_244134,RMVar_hsa_circ_281398,RMVar_hsa_circ_244135,RMVar_hsa_circ_316474,RMVar_hsa_circ_244137 32729 RMVar_ID_32729 Human_SNP_ID_313679294 A-to-I Human chr7 - 23517693 23517693 23517693 TGGCGAGGATGGTCTCGATCTCTTGACCTCGTAATCTGCCTGCCTCGGCCTCCCAAAGTACTGGG TGGCGAGGATGGTCTCGATCTCTTGACCTCGTGATCTGCCTGCCTCGGCCTCCCAAAGTACTGGG T C TRA2A Ensembl:ENSG00000164548 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs944887723 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16117504 RMVar_hsa_circ_8969,RMVar_hsa_circ_69534,RMVar_hsa_circ_283918,RMVar_hsa_circ_355766,RMVar_hsa_circ_244132,RMVar_hsa_circ_361566,RMVar_hsa_circ_244134,RMVar_hsa_circ_281398,RMVar_hsa_circ_244135,RMVar_hsa_circ_316474,RMVar_hsa_circ_244137 32730 RMVar_ID_32730 Human_SNP_ID_313679337 A-to-I Human chr7 - 23517812 23517812 23517812 CACCTCCCGGGTTCAAGTGATTCTCGTGCCTCAGCCTCCCAAGTAGCTGGGATGACAGGTGTGCG CACCTCCCGGGTTCAAGTGATTCTCGTGCCTCGGCCTCCCAAGTAGCTGGGATGACAGGTGTGCG T C TRA2A Ensembl:ENSG00000164548 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs990881287 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8969,RMVar_hsa_circ_69534,RMVar_hsa_circ_283918,RMVar_hsa_circ_355766,RMVar_hsa_circ_244132,RMVar_hsa_circ_361566,RMVar_hsa_circ_244134,RMVar_hsa_circ_281398,RMVar_hsa_circ_244135,RMVar_hsa_circ_316474,RMVar_hsa_circ_244137 32731 RMVar_ID_32731 Human_SNP_ID_313679413 A-to-I Human chr7 - 23518059 23518059 23518059 TGGTGCATGCCTGTAGTCCTAGCTGTCTGGGAAGCTGAGGTGGAAGAATTTCTTGAGCCTGGGAG TGGTGCATGCCTGTAGTCCTAGCTGTCTGGGATGCTGAGGTGGAAGAATTTCTTGAGCCTGGGAG T A TRA2A Ensembl:ENSG00000164548 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1244787705 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7725059,Human_RBP_ID_26093813 RMVar_hsa_circ_8969,RMVar_hsa_circ_69534,RMVar_hsa_circ_283918,RMVar_hsa_circ_355766,RMVar_hsa_circ_244132,RMVar_hsa_circ_361566,RMVar_hsa_circ_244134,RMVar_hsa_circ_281398,RMVar_hsa_circ_244135,RMVar_hsa_circ_316474,RMVar_hsa_circ_244137 32732 RMVar_ID_32732 Human_SNP_ID_313679734 A-to-I Human chr7 - 23519137 23519137 23519137 TGCCTGCCTCGGCCTCCCAAAGGGCTGGGATTACAGGCGTGAGCCACCGTGCCCGGCCTGTCGGA TGCCTGCCTCGGCCTCCCAAAGGGCTGGGATTGCAGGCGTGAGCCACCGTGCCCGGCCTGTCGGA T C TRA2A Ensembl:ENSG00000164548 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1164243580 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26093826 RMVar_hsa_circ_8969,RMVar_hsa_circ_69534,RMVar_hsa_circ_283918,RMVar_hsa_circ_355766,RMVar_hsa_circ_244132,RMVar_hsa_circ_361566,RMVar_hsa_circ_244134,RMVar_hsa_circ_281398,RMVar_hsa_circ_244135,RMVar_hsa_circ_316474,RMVar_hsa_circ_244137 32733 RMVar_ID_32733 Human_SNP_ID_313679765 A-to-I Human chr7 - 23519235 23519235 23519235 CACACGCCACCAACACCCAGCTAATTTTTTGTATTTTTAATAGAGACGGGGTTTTATCATGTTAG CACACGCCACCAACACCCAGCTAATTTTTTGTGTTTTTAATAGAGACGGGGTTTTATCATGTTAG T C TRA2A Ensembl:ENSG00000164548 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1212378431 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8969,RMVar_hsa_circ_69534,RMVar_hsa_circ_283918,RMVar_hsa_circ_355766,RMVar_hsa_circ_244132,RMVar_hsa_circ_361566,RMVar_hsa_circ_244134,RMVar_hsa_circ_281398,RMVar_hsa_circ_244135,RMVar_hsa_circ_316474,RMVar_hsa_circ_244137 32734 RMVar_ID_32734 Human_SNP_ID_313679786 A-to-I Human chr7 - 23519294 23519294 23519294 TGCCTCTCTGGTTCAAGTGATTCTCTTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCACACG TGCCTCTCTGGTTCAAGTGATTCTCTTGCCTCTGCCTCCCGAGTAGCTGGGATTACAGGCACACG T A TRA2A Ensembl:ENSG00000164548 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1386063343 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8969,RMVar_hsa_circ_69534,RMVar_hsa_circ_283918,RMVar_hsa_circ_355766,RMVar_hsa_circ_244132,RMVar_hsa_circ_361566,RMVar_hsa_circ_244134,RMVar_hsa_circ_281398,RMVar_hsa_circ_244135,RMVar_hsa_circ_316474,RMVar_hsa_circ_244137 32735 RMVar_ID_32735 Human_SNP_ID_313679793 A-to-I Human chr7 - 23519311 23519303 23519312 GGCCTCACTGCAATGTCTGCCTCTCTGGTTCAAGTGATTCTCTTGCCTCAGCCTCCCGAGTAGCT GGCCTCACTGCAATGTCTGCCTCTCTGGTTC_________TCTTGCCTCAGCCTCCCGAGTAGCT AGAATCACTT A TRA2A Ensembl:ENSG00000164548 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1247734432 Functional Loss DEL dbSNP153 32..40 33 - - - RMVar_hsa_circ_8969,RMVar_hsa_circ_69534,RMVar_hsa_circ_283918,RMVar_hsa_circ_355766,RMVar_hsa_circ_244132,RMVar_hsa_circ_361566,RMVar_hsa_circ_244134,RMVar_hsa_circ_281398,RMVar_hsa_circ_244135,RMVar_hsa_circ_316474,RMVar_hsa_circ_244137 32736 RMVar_ID_32736 Human_SNP_ID_313680035 A-to-I Human chr7 - 23520133 23520133 23520133 TGGCTCACTGCAACCTCCACCTCCCGGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCCGAGTAGCT TGGCTCACTGCAACCTCCACCTCCCGGGTTCATGCAGTTCTCCTGCCTCAGCCTCCCGAGTAGCT T A TRA2A Ensembl:ENSG00000164548 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1054209069 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8969,RMVar_hsa_circ_69534,RMVar_hsa_circ_283918,RMVar_hsa_circ_355766,RMVar_hsa_circ_244132,RMVar_hsa_circ_361566,RMVar_hsa_circ_244134,RMVar_hsa_circ_281398,RMVar_hsa_circ_244135,RMVar_hsa_circ_316474,RMVar_hsa_circ_244137 32737 RMVar_ID_32737 Human_SNP_ID_313680280 A-to-I Human chr7 - 23520869 23520869 23520869 GGGCAACATGGTGAAACCCTGCCTCTACTACAAATACAAAAATTAGCTGGGCGGGGTGGCGGGCA GGGCAACATGGTGAAACCCTGCCTCTACTACAGATACAAAAATTAGCTGGGCGGGGTGGCGGGCA T C TRA2A Ensembl:ENSG00000164548 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1025066479 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8969,RMVar_hsa_circ_69534,RMVar_hsa_circ_283918,RMVar_hsa_circ_355766,RMVar_hsa_circ_244132,RMVar_hsa_circ_361566,RMVar_hsa_circ_244134,RMVar_hsa_circ_281398,RMVar_hsa_circ_244135,RMVar_hsa_circ_316474,RMVar_hsa_circ_244137 32738 RMVar_ID_32738 Human_SNP_ID_313680293 A-to-I Human chr7 - 23520920 23520920 23520920 GGGAAGCCGAGGTGGGTAGATAACTTGAGGTCAGGAGTTTTAGACCAGCCTGGGCAACATGGTGA GGGAAGCCGAGGTGGGTAGATAACTTGAGGTCGGGAGTTTTAGACCAGCCTGGGCAACATGGTGA T C TRA2A Ensembl:ENSG00000164548 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs990077685 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16117587 RMVar_hsa_circ_8969,RMVar_hsa_circ_69534,RMVar_hsa_circ_283918,RMVar_hsa_circ_355766,RMVar_hsa_circ_244132,RMVar_hsa_circ_361566,RMVar_hsa_circ_244134,RMVar_hsa_circ_281398,RMVar_hsa_circ_244135,RMVar_hsa_circ_316474,RMVar_hsa_circ_244137 32739 RMVar_ID_32739 Human_SNP_ID_313680294 A-to-I Human chr7 - 23520920 23520920 23520920 GGGAAGCCGAGGTGGGTAGATAACTTGAGGTCAGGAGTTTTAGACCAGCCTGGGCAACATGGTGA GGGAAGCCGAGGTGGGTAGATAACTTGAGGTCCGGAGTTTTAGACCAGCCTGGGCAACATGGTGA T G TRA2A Ensembl:ENSG00000164548 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs990077685 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16117587 RMVar_hsa_circ_8969,RMVar_hsa_circ_69534,RMVar_hsa_circ_283918,RMVar_hsa_circ_355766,RMVar_hsa_circ_244132,RMVar_hsa_circ_361566,RMVar_hsa_circ_244134,RMVar_hsa_circ_281398,RMVar_hsa_circ_244135,RMVar_hsa_circ_316474,RMVar_hsa_circ_244137 32740 RMVar_ID_32740 Human_SNP_ID_313680303 A-to-I Human chr7 - 23520966 23520946 23520967 AAGACAGGCTGGGTGCAGTGGCTCACACCTGTAATACCAACACTTTGGGAAGCCGAGGTGGGTAG AAGACAGGCTGGGTGCAGTGGCTCACACCTG_____________________CCGAGGTGGGTAG GCTTCCCAAAGTGTTGGTATTA G TRA2A Ensembl:ENSG00000164548 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1234427393 Functional Loss DEL dbSNP153 32..52 33 - - - Human_RBP_ID_16117589 RMVar_hsa_circ_8969,RMVar_hsa_circ_69534,RMVar_hsa_circ_283918,RMVar_hsa_circ_355766,RMVar_hsa_circ_244132,RMVar_hsa_circ_361566,RMVar_hsa_circ_244134,RMVar_hsa_circ_281398,RMVar_hsa_circ_244135,RMVar_hsa_circ_316474,RMVar_hsa_circ_244137 32741 RMVar_ID_32741 Human_SNP_ID_313691915 A-to-I Human chr7 - 23564141 23564141 23564141 CCTGTAGTTCAAATGGGAGAATTATGCATAGAAGTTACACCCCAGAGCAAAATAGCATGGATTTC CCTGTAGTTCAAATGGGAGAATTATGCATAGAGGTTACACCCCAGAGCAAAATAGCATGGATTTC T C AC006026.1 Ensembl:ENSG00000224785 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049267824 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4935741 32742 RMVar_ID_32742 Human_SNP_ID_313705590 A-to-I Human chr7 + 23613190 23613190 23613190 AAAGTTAGTGGGGCGTGGTGGCGCGCACTTGTAGTTCCAGCTACTTGGGAGGTTCAGGTGGGACA AAAGTTAGTGGGGCGTGGTGGCGCGCACTTGTGGTTCCAGCTACTTGGGAGGTTCAGGTGGGACA A G CCDC126 Ensembl:ENSG00000169193 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs983024041 Functional Loss SNV dbSNP153 33..33 33 - - - 32743 RMVar_ID_32743 Human_SNP_ID_313706445 A-to-I Human chr7 + 23617221 23617221 23617221 AATACGAAAATTATCTGGACGTGGTGGCACACACCTGTAATCCTAGCTACTCGGGAGGCTGAGGC AATACGAAAATTATCTGGACGTGGTGGCACACGCCTGTAATCCTAGCTACTCGGGAGGCTGAGGC A G CCDC126 Ensembl:ENSG00000169193 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs962044231 Functional Loss SNV dbSNP153 33..33 33 - - - 32744 RMVar_ID_32744 Human_SNP_ID_313706448 A-to-I Human chr7 + 23617227 23617227 23617227 AAAATTATCTGGACGTGGTGGCACACACCTGTAATCCTAGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTATCTGGACGTGGTGGCACACACCTGTGATCCTAGCTACTCGGGAGGCTGAGGCAGGAGA A G CCDC126 Ensembl:ENSG00000169193 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1295643927 Functional Loss SNV dbSNP153 33..33 33 - - - 32745 RMVar_ID_32745 Human_SNP_ID_313706861 A-to-I Human chr7 + 23618690 23618690 23618690 CTCCTGCCTCAGCCTCCCGAGAACCTGGGACTACAGGCATGCACCACCGCGCCCAGCTAATTTTT CTCCTGCCTCAGCCTCCCGAGAACCTGGGACTTCAGGCATGCACCACCGCGCCCAGCTAATTTTT A T CCDC126 Ensembl:ENSG00000169193 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348715051 Functional Loss SNV dbSNP153 33..33 33 - - - 32746 RMVar_ID_32746 Human_SNP_ID_313708139 A-to-I Human chr7 + 23623043 23623043 23623043 TTGCCCAGGCTGGAGTGCAATGGCACAATCTCAGCTCACTGCAGCCTCTGCCTCCCGGGTTCAGG TTGCCCAGGCTGGAGTGCAATGGCACAATCTCTGCTCACTGCAGCCTCTGCCTCCCGGGTTCAGG A T CCDC126 Ensembl:ENSG00000169193 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1488762514 Functional Loss SNV dbSNP153 33..33 33 - - - 32747 RMVar_ID_32747 Human_SNP_ID_313708286 A-to-I Human chr7 + 23623473 23623473 23623473 ACAAAGTTGGCCAGGTGTGGCGTTGCTTGCCTATAGTCCCTGCTGCTGTGGAGGCTGAGGCAGGA ACAAAGTTGGCCAGGTGTGGCGTTGCTTGCCTGTAGTCCCTGCTGCTGTGGAGGCTGAGGCAGGA A G CCDC126 Ensembl:ENSG00000169193 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1300834144 Functional Loss SNV dbSNP153 33..33 33 - - - 32748 RMVar_ID_32748 Human_SNP_ID_313708296 A-to-I Human chr7 + 23623511 23623511 23623511 CCTGCTGCTGTGGAGGCTGAGGCAGGAGAGTCACTTGAACCCAGAAGGCAGAGGTTGTGGTGGGC CCTGCTGCTGTGGAGGCTGAGGCAGGAGAGTCGCTTGAACCCAGAAGGCAGAGGTTGTGGTGGGC A G CCDC126 Ensembl:ENSG00000169193 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215299362 Functional Loss SNV dbSNP153 33..33 33 - - - 32749 RMVar_ID_32749 Human_SNP_ID_313708299 A-to-I Human chr7 + 23623521 23623521 23623521 TGGAGGCTGAGGCAGGAGAGTCACTTGAACCCAGAAGGCAGAGGTTGTGGTGGGCCGAAGTTGTG TGGAGGCTGAGGCAGGAGAGTCACTTGAACCCCGAAGGCAGAGGTTGTGGTGGGCCGAAGTTGTG A C CCDC126 Ensembl:ENSG00000169193 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1220395588 Functional Loss SNV dbSNP153 33..33 33 - - - 32750 RMVar_ID_32750 Human_SNP_ID_313708675 A-to-I Human chr7 + 23625065 23625065 23625065 AGGGTCTCACTGTGTTGCCCGGCATATTCTCAAACTTCTGGAATCAAGCGATCCTCCCACCTTGG AGGGTCTCACTGTGTTGCCCGGCATATTCTCACACTTCTGGAATCAAGCGATCCTCCCACCTTGG A C CCDC126 Ensembl:ENSG00000169193 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1433448567 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21478535 32751 RMVar_ID_32751 Human_SNP_ID_313708683 A-to-I Human chr7 + 23625104 23625104 23625104 GGAATCAAGCGATCCTCCCACCTTGGCTTCCCAAAGTGCTCGGATTACAGATGTGAGCTACTATG GGAATCAAGCGATCCTCCCACCTTGGCTTCCCGAAGTGCTCGGATTACAGATGTGAGCTACTATG A G CCDC126 Ensembl:ENSG00000169193 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202987599 Functional Loss SNV dbSNP153 33..33 33 - - - 32752 RMVar_ID_32752 Human_SNP_ID_313710064 A-to-I Human chr7 + 23630352 23630352 23630352 GAAACCCCATCTCTACTAAAAATACAAAAATTAGCTGCTTGTGGTTGTGCACGCCTGTAATTCCA GAAACCCCATCTCTACTAAAAATACAAAAATTCGCTGCTTGTGGTTGTGCACGCCTGTAATTCCA A C CCDC126 Ensembl:ENSG00000169193 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs948677327 Functional Loss SNV dbSNP153 33..33 33 - - - 32753 RMVar_ID_32753 Human_SNP_ID_313710080 A-to-I Human chr7 + 23630405 23630405 23630405 CCTGTAATTCCAGCTACTCAGGAGGCTGAGGTATGAGAATTGCTTGAACCGGGAGACAGAGGTTG CCTGTAATTCCAGCTACTCAGGAGGCTGAGGTGTGAGAATTGCTTGAACCGGGAGACAGAGGTTG A G CCDC126 Ensembl:ENSG00000169193 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355698960 Functional Loss SNV dbSNP153 33..33 33 - - - 32754 RMVar_ID_32754 Human_SNP_ID_313713057 A-to-I Human chr7 + 23639321 23639321 23639321 TCAAGCAGTTCTTCTGCTTCAGCCTCCCGAGTAGCTGGGACTACAGACATGTGCCATCACGCCTG TCAAGCAGTTCTTCTGCTTCAGCCTCCCGAGTGGCTGGGACTACAGACATGTGCCATCACGCCTG A G CCDC126 Ensembl:ENSG00000169193 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1225181646 Functional Loss SNV dbSNP153 33..33 33 - - - 32755 RMVar_ID_32755 Human_SNP_ID_313713060 A-to-I Human chr7 + 23639331 23639331 23639331 CTTCTGCTTCAGCCTCCCGAGTAGCTGGGACTACAGACATGTGCCATCACGCCTGGGCTAATTTT CTTCTGCTTCAGCCTCCCGAGTAGCTGGGACTGCAGACATGTGCCATCACGCCTGGGCTAATTTT A G CCDC126 Ensembl:ENSG00000169193 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs918733711 Functional Loss SNV dbSNP153 33..33 33 - - - 32756 RMVar_ID_32756 Human_SNP_ID_313713090 A-to-I Human chr7 + 23639438 23639438 23639438 GGTGGCCAGGCTGGTCTTGAATGCCTGACCTCAAGTGATCCATCCTGCCTCGGCCGCCCAAAGTG GGTGGCCAGGCTGGTCTTGAATGCCTGACCTCCAGTGATCCATCCTGCCTCGGCCGCCCAAAGTG A C CCDC126 Ensembl:ENSG00000169193 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417100332 Functional Loss SNV dbSNP153 33..33 33 - - - 32757 RMVar_ID_32757 Human_SNP_ID_313713113 A-to-I Human chr7 + 23639479 23639479 23639479 ATCCTGCCTCGGCCGCCCAAAGTGCTGGGATTACAGGCGTGAGCCATCGCACCCAGTCCTCTTTA ATCCTGCCTCGGCCGCCCAAAGTGCTGGGATTGCAGGCGTGAGCCATCGCACCCAGTCCTCTTTA A G CCDC126 Ensembl:ENSG00000169193 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1203891285 Functional Loss SNV dbSNP153 33..33 33 - - - 32758 RMVar_ID_32758 Human_SNP_ID_313713413 A-to-I Human chr7 + 23640376 23640376 23640376 AAAATTAGCCAGGCATGGTGTTGCATGCCTGTAATCCCAGCTACTCGGGAGACTGACGCAGGCGA AAAATTAGCCAGGCATGGTGTTGCATGCCTGTGATCCCAGCTACTCGGGAGACTGACGCAGGCGA A G CCDC126 Ensembl:ENSG00000169193 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs936395485 Functional Loss SNV dbSNP153 33..33 33 - - - 32759 RMVar_ID_32759 Human_SNP_ID_313713423 A-to-I Human chr7 + 23640403 23640403 23640403 CCTGTAATCCCAGCTACTCGGGAGACTGACGCAGGCGAATCACTTGTACCTGGGAGGTGGAGGTT CCTGTAATCCCAGCTACTCGGGAGACTGACGCGGGCGAATCACTTGTACCTGGGAGGTGGAGGTT A G CCDC126 Ensembl:ENSG00000169193 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs906811366 Functional Loss SNV dbSNP153 33..33 33 - - - 32760 RMVar_ID_32760 Human_SNP_ID_313959744 A-to-I Human chr7 + 24616391 24616391 24616391 AAAATAAATACACAAAAATCAGTAGTATTTCTATATACAAACAACACACATTAAAAATCAAGAAA AAAATAAATACACAAAAATCAGTAGTATTTCTGTATACAAACAACACACATTAAAAATCAAGAAA A G MPP6 Ensembl:ENSG00000105926 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1447179588 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84425,RMVar_hsa_circ_89409,RMVar_hsa_circ_88166,RMVar_hsa_circ_244153,RMVar_hsa_circ_244154,RMVar_hsa_circ_244152 32761 RMVar_ID_32761 Human_SNP_ID_313986517 A-to-I Human chr7 - 24711649 24711649 24711649 GACCATGCCCAGCTCATTTTAAATTTTTTTGTAGAGACGGGGTCTCACTATGTTGCTACTCTCAA GACCATGCCCAGCTCATTTTAAATTTTTTTGTGGAGACGGGGTCTCACTATGTTGCTACTCTCAA T C GSDME Ensembl:ENSG00000105928 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1476556187 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50886,RMVar_hsa_circ_48686 32762 RMVar_ID_32762 Human_SNP_ID_314007873 A-to-I Human chr7 - 24798336 24798336 24798336 AAACAAATGTAGTTTCCACAGTGTGAGGATAAATGTAGAATCGTGGTAATATTGGCTGTTAAATT AAACAAATGTAGTTTCCACAGTGTGAGGATAAGTGTAGAATCGTGGTAATATTGGCTGTTAAATT T C OSBPL3 Ensembl:ENSG00000070882 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs902731371 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16121675,Human_RBP_ID_24208490 RMVar_hsa_circ_267408 32763 RMVar_ID_32763 Human_SNP_ID_314008354 A-to-I Human chr7 - 24800562 24800562 24800562 GTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGATTGAACCTGGGAAGCAGAGGTTGCAGTG GTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAGTCGATTGAACCTGGGAAGCAGAGGTTGCAGTG T C OSBPL3 Ensembl:ENSG00000070882 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1470510433 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267408 32764 RMVar_ID_32764 Human_SNP_ID_314008376 A-to-I Human chr7 - 24800636 24800636 24800636 CCTAGCCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGTCGGGCATGGTTGCAC CCTAGCCAACATGGTGAAACCCCGTCTCTACTGAAAATACAAAAATTAGTCGGGCATGGTTGCAC T C OSBPL3 Ensembl:ENSG00000070882 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs924264323 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267408 32765 RMVar_ID_32765 Human_SNP_ID_314013617 A-to-I Human chr7 - 24822417 24822417 24822417 ATGGTTATTATTATTATAGATAGTGTCTCACTATGTTGCCCAGGCTGGTCTTGAACTCCTGGATC ATGGTTATTATTATTATAGATAGTGTCTCACTGTGTTGCCCAGGCTGGTCTTGAACTCCTGGATC T C OSBPL3 Ensembl:ENSG00000070882 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs931609943 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_62944,RMVar_hsa_circ_267408,RMVar_hsa_circ_336141,RMVar_hsa_circ_65793,RMVar_hsa_circ_21893,RMVar_hsa_circ_13034,RMVar_hsa_circ_350986,RMVar_hsa_circ_97853,RMVar_hsa_circ_244199,RMVar_hsa_circ_337224,RMVar_hsa_circ_337433,RMVar_hsa_circ_244201,RMVar_hsa_circ_344277,RMVar_hsa_circ_344747,RMVar_hsa_circ_338992,RMVar_hsa_circ_36329,RMVar_hsa_circ_14773,RMVar_hsa_circ_50749,RMVar_hsa_circ_244202 32766 RMVar_ID_32766 Human_SNP_ID_314014895 A-to-I Human chr7 - 24828425 24828425 24828425 TTTTGTATTTTTAATAGAGATGGCATTTCACCATATTGGCCGGGCTGGTCGCAAACTGACCTCAT TTTTGTATTTTTAATAGAGATGGCATTTCACCGTATTGGCCGGGCTGGTCGCAAACTGACCTCAT T C OSBPL3 Ensembl:ENSG00000070882 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1173194863 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_62944,RMVar_hsa_circ_267408,RMVar_hsa_circ_336141,RMVar_hsa_circ_65793,RMVar_hsa_circ_21893,RMVar_hsa_circ_13034,RMVar_hsa_circ_350986,RMVar_hsa_circ_97853,RMVar_hsa_circ_244199,RMVar_hsa_circ_337224,RMVar_hsa_circ_337433,RMVar_hsa_circ_244201,RMVar_hsa_circ_344277,RMVar_hsa_circ_344747,RMVar_hsa_circ_338992,RMVar_hsa_circ_36329,RMVar_hsa_circ_14773,RMVar_hsa_circ_50749,RMVar_hsa_circ_244202 32767 RMVar_ID_32767 Human_SNP_ID_314017185 A-to-I Human chr7 - 24837403 24837403 24837403 GGCCAAGAGTTTGAGACCAGCCTGCGCAACATAGCAAGATCCTGTCTCTAAAAAAGATACAAAAA GGCCAAGAGTTTGAGACCAGCCTGCGCAACATGGCAAGATCCTGTCTCTAAAAAAGATACAAAAA T C OSBPL3 Ensembl:ENSG00000070882 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1284822548 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_62944,RMVar_hsa_circ_267408,RMVar_hsa_circ_65793,RMVar_hsa_circ_21893,RMVar_hsa_circ_350986,RMVar_hsa_circ_97853,RMVar_hsa_circ_244199,RMVar_hsa_circ_20553,RMVar_hsa_circ_344747,RMVar_hsa_circ_338992,RMVar_hsa_circ_14773,RMVar_hsa_circ_50749,RMVar_hsa_circ_244202,RMVar_hsa_circ_345468,RMVar_hsa_circ_374955,RMVar_hsa_circ_324489,RMVar_hsa_circ_61974,RMVar_hsa_circ_244204,RMVar_hsa_circ_244205,RMVar_hsa_circ_244206 32768 RMVar_ID_32768 Human_SNP_ID_314088049 A-to-I Human chr7 - 25119405 25119405 25119405 TGGGCGTGGTGGCGGCACCTGTAATTGCAGCTATTTGAGAGGCTGAGGCAGGAGAATCGCTTGAA TGGGCGTGGTGGCGGCACCTGTAATTGCAGCTGTTTGAGAGGCTGAGGCAGGAGAATCGCTTGAA T C CYCS Ensembl:ENSG00000172115 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs547040009 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23075288 32769 RMVar_ID_32769 Human_SNP_ID_314088050 A-to-I Human chr7 - 25119414 25119414 25119414 AAAACTAGCTGGGCGTGGTGGCGGCACCTGTAATTGCAGCTATTTGAGAGGCTGAGGCAGGAGAA AAAACTAGCTGGGCGTGGTGGCGGCACCTGTAGTTGCAGCTATTTGAGAGGCTGAGGCAGGAGAA T C CYCS Ensembl:ENSG00000172115 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1022228957 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23075288 32770 RMVar_ID_32770 Human_SNP_ID_314088051 A-to-I Human chr7 - 25119414 25119414 25119414 AAAACTAGCTGGGCGTGGTGGCGGCACCTGTAATTGCAGCTATTTGAGAGGCTGAGGCAGGAGAA AAAACTAGCTGGGCGTGGTGGCGGCACCTGTACTTGCAGCTATTTGAGAGGCTGAGGCAGGAGAA T G CYCS Ensembl:ENSG00000172115 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1022228957 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23075288 32771 RMVar_ID_32771 Human_SNP_ID_314088067 A-to-I Human chr7 - 25119446 25119446 25119446 CATGGTGAAACCCCATCTCTACCAAAAATATAAAAACTAGCTGGGCGTGGTGGCGGCACCTGTAA CATGGTGAAACCCCATCTCTACCAAAAATATATAAACTAGCTGGGCGTGGTGGCGGCACCTGTAA T A CYCS Ensembl:ENSG00000172115 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991881225 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26094853 32772 RMVar_ID_32772 Human_SNP_ID_314088283 A-to-I Human chr7 - 25120188 25120188 25120188 TCAGCTACTTGGGAGGCTGAGGCACAAGAATCACTTGAACTTGGGAGGTGGAGGTTGCAGTGAGC TCAGCTACTTGGGAGGCTGAGGCACAAGAATCGCTTGAACTTGGGAGGTGGAGGTTGCAGTGAGC T C CYCS Ensembl:ENSG00000172115 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1137513 Functional Loss SNV dbSNP153 33..33 33 - - - 32773 RMVar_ID_32773 Human_SNP_ID_314088320 A-to-I Human chr7 - 25120313 25120313 25120313 GGGAGGCCAAGGCAGGCAGATCACTTGAGGTCAGGCGTTTGAGACCAGCCTGGTCAACATGGCGA GGGAGGCCAAGGCAGGCAGATCACTTGAGGTCTGGCGTTTGAGACCAGCCTGGTCAACATGGCGA T A CYCS Ensembl:ENSG00000172115 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1137509 Functional Loss SNV dbSNP153 33..33 33 - - - 32774 RMVar_ID_32774 Human_SNP_ID_314088321 A-to-I Human chr7 - 25120313 25120313 25120313 GGGAGGCCAAGGCAGGCAGATCACTTGAGGTCAGGCGTTTGAGACCAGCCTGGTCAACATGGCGA GGGAGGCCAAGGCAGGCAGATCACTTGAGGTCGGGCGTTTGAGACCAGCCTGGTCAACATGGCGA T C CYCS Ensembl:ENSG00000172115 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1137509 Functional Loss SNV dbSNP153 33..33 33 - - - 32775 RMVar_ID_32775 Human_SNP_ID_314088495 A-to-I Human chr7 - 25120903 25120903 25120903 ACAGGCTGGTCTTGAACTCCCGACGTCAGGTGATCTACCTGCCTCGGCCTCCCAAAGTGCTGGGA ACAGGCTGGTCTTGAACTCCCGACGTCAGGTGGTCTACCTGCCTCGGCCTCCCAAAGTGCTGGGA T C CYCS Ensembl:ENSG00000172115 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025023699 Functional Loss SNV dbSNP153 33..33 33 - - - 32776 RMVar_ID_32776 Human_SNP_ID_314088496 A-to-I Human chr7 - 25120908 25120908 25120908 GCTGGACAGGCTGGTCTTGAACTCCCGACGTCAGGTGATCTACCTGCCTCGGCCTCCCAAAGTGC GCTGGACAGGCTGGTCTTGAACTCCCGACGTCGGGTGATCTACCTGCCTCGGCCTCCCAAAGTGC T C CYCS Ensembl:ENSG00000172115 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1219404093 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16122742,Human_RBP_ID_26094863 32777 RMVar_ID_32777 Human_SNP_ID_314088548 A-to-I Human chr7 - 25121041 25121041 25121041 CTGCTCACCGCAACCTCCGCCTTCCAGGTTCAAGCGATTCTCCTGACTCAGCCTCTCAAGTAGCT CTGCTCACCGCAACCTCCGCCTTCCAGGTTCATGCGATTCTCCTGACTCAGCCTCTCAAGTAGCT T A CYCS Ensembl:ENSG00000172115 Protein coding 3'UTR GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 29129909,30559470 RNA-Seq:(High) rs1280743740 Functional Loss SNV dbSNP153 33..33 33 - - - 32778 RMVar_ID_32778 Human_SNP_ID_314088643 A-to-I Human chr7 - 25121351 25121351 25121351 TTTAGTGGAGATGGTGTTTCACCATGTTGGCCAGACTGGTCTTGGACTCCTGACCTCGTGATCCA TTTAGTGGAGATGGTGTTTCACCATGTTGGCCGGACTGGTCTTGGACTCCTGACCTCGTGATCCA T C CYCS Ensembl:ENSG00000172115 Protein coding 3'UTR GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs908866556 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16122757 32779 RMVar_ID_32779 Human_SNP_ID_314088663 A-to-I Human chr7 - 25121421 25121421 25121421 CTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCACCCGCCACCACGCCTGGCTAATTTTT CTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTCCAGGCACCCGCCACCACGCCTGGCTAATTTTT T G CYCS Ensembl:ENSG00000172115 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1437157104 Functional Loss SNV dbSNP153 33..33 33 - - - 32780 RMVar_ID_32780 Human_SNP_ID_314088804 A-to-I Human chr7 - 25121864 25121864 25121864 GGAGTGCAGTGGTGCGATCTCGGCTGGCTGCAACCTCTATTTCCCAGGCTCAAGCGATTCTCTCA GGAGTGCAGTGGTGCGATCTCGGCTGGCTGCAGCCTCTATTTCCCAGGCTCAAGCGATTCTCTCA T C CYCS Ensembl:ENSG00000172115 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1283132075 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16122779 32781 RMVar_ID_32781 Human_SNP_ID_314088817 A-to-I Human chr7 - 25121889 25121889 25121889 ATGGTCACGCTGTGTCGCCAAGGCTGGAGTGCAGTGGTGCGATCTCGGCTGGCTGCAACCTCTAT ATGGTCACGCTGTGTCGCCAAGGCTGGAGTGCCGTGGTGCGATCTCGGCTGGCTGCAACCTCTAT T G CYCS Ensembl:ENSG00000172115 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1156498471 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16122780,Human_RBP_ID_18184496 Human_miRNA_ID_622177 32782 RMVar_ID_32782 Human_SNP_ID_314347493 A-to-I Human chr7 + 26158112 26158112 26158112 GCTCTGTCTCCCAGGCTGGAATTCAATGGCGCAATCTCGGCTCACTGCAACCTCTGCCTCCCAGG GCTCTGTCTCCCAGGCTGGAATTCAATGGCGCGATCTCGGCTCACTGCAACCTCTGCCTCCCAGG A G NFE2L3 Ensembl:ENSG00000050344 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs899434689 Functional Loss SNV dbSNP153 33..33 33 - - - 32783 RMVar_ID_32783 Human_SNP_ID_314350711 A-to-I Human chr7 - 26171004 26171004 26171004 ATCTGATAGATGAAAACTGGTGATCATGGCTTACTGCAGCCTCAAACTCTTGGGCTCAAGTGATC ATCTGATAGATGAAAACTGGTGATCATGGCTTCCTGCAGCCTCAAACTCTTGGGCTCAAGTGATC T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982680213 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16123304,Human_RBP_ID_18880759 RMVar_hsa_circ_244214 32784 RMVar_ID_32784 Human_SNP_ID_314350789 A-to-I Human chr7 - 26171302 26171302 26171302 TGACTTCAGGTGATCCACCTGCCAGCCTCCCAAAGTACTGGGATTACAGGCATGAACCACCACGC TGACTTCAGGTGATCCACCTGCCAGCCTCCCACAGTACTGGGATTACAGGCATGAACCACCACGC T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1400812877 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_244214 32785 RMVar_ID_32785 Human_SNP_ID_314354702 A-to-I Human chr7 - 26182576 26182576 26182576 TCGCCCAGGCTGGAGAGCACTGGTGAGATCTCAGCTCACTGCAATCTCCGCCTCCTGGGTTCAAG TCGCCCAGGCTGGAGAGCACTGGTGAGATCTCGGCTCACTGCAATCTCCGCCTCCTGGGTTCAAG T C HNRNPA2B1 Ensembl:ENSG00000122566 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs950281944 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16123704 32786 RMVar_ID_32786 Human_SNP_ID_314354856 A-to-I Human chr7 - 26182886 26182862 26182887 GGGATGGTGAGGCAGGAGGACTGCCTGAGTCCAGGAGGTTGAGGCTGCAGTGAGTCGTGACAGCG GGGATGGTGAGGCAGGAGGACTGCCTGAGTC_________________________GTGACAGCG CGACTCACTGCAGCCTCAACCTCCTG C HNRNPA2B1 Ensembl:ENSG00000122566 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1562678574 Functional Loss DEL dbSNP153 32..56 33 - - - Human_RBP_ID_16123716,Human_RBP_ID_26095062 32787 RMVar_ID_32787 Human_SNP_ID_314354867 A-to-I Human chr7 - 26182886 26182886 26182886 GGGATGGTGAGGCAGGAGGACTGCCTGAGTCCAGGAGGTTGAGGCTGCAGTGAGTCGTGACAGCG GGGATGGTGAGGCAGGAGGACTGCCTGAGTCCGGGAGGTTGAGGCTGCAGTGAGTCGTGACAGCG T C HNRNPA2B1 Ensembl:ENSG00000122566 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs988705789 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16123716,Human_RBP_ID_26095062 32788 RMVar_ID_32788 Human_SNP_ID_314355052 A-to-I Human chr7 - 26183322 26183322 26183322 GTTGGTCTCGAACTTTTGACCGCAAGTGATCCACCCACCTAGGCCTCCCAAAGTGCTGGGATTAC GTTGGTCTCGAACTTTTGACCGCAAGTGATCCTCCCACCTAGGCCTCCCAAAGTGCTGGGATTAC T A HNRNPA2B1 Ensembl:ENSG00000122566 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1263514805 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16123732 32789 RMVar_ID_32789 Human_SNP_ID_314355053 A-to-I Human chr7 - 26183322 26183322 26183322 GTTGGTCTCGAACTTTTGACCGCAAGTGATCCACCCACCTAGGCCTCCCAAAGTGCTGGGATTAC GTTGGTCTCGAACTTTTGACCGCAAGTGATCCGCCCACCTAGGCCTCCCAAAGTGCTGGGATTAC T C HNRNPA2B1 Ensembl:ENSG00000122566 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1263514805 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16123732 32790 RMVar_ID_32790 Human_SNP_ID_314355129 A-to-I Human chr7 - 26183436 26183436 26183436 TCAAAGGATTCTCCTGCCTTAGCCTCCGGAGTAGCTGGGATTACAGCTGTGCACCACCACGTCTG TCAAAGGATTCTCCTGCCTTAGCCTCCGGAGTGGCTGGGATTACAGCTGTGCACCACCACGTCTG T C HNRNPA2B1 Ensembl:ENSG00000122566 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1406151088 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16123738 32791 RMVar_ID_32791 Human_SNP_ID_314355143 A-to-I Human chr7 - 26183472 26183472 26183472 GCAATCTCGGCTCACTACACCCTCTGCCTCCCAGGTTCAAAGGATTCTCCTGCCTTAGCCTCCGG GCAATCTCGGCTCACTACACCCTCTGCCTCCCCGGTTCAAAGGATTCTCCTGCCTTAGCCTCCGG T G HNRNPA2B1 Ensembl:ENSG00000122566 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs888777124 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16123740 32792 RMVar_ID_32792 Human_SNP_ID_314355150 A-to-I Human chr7 - 26183488 26183488 26183488 AATGGAGTGCAGTGGTGCAATCTCGGCTCACTACACCCTCTGCCTCCCAGGTTCAAAGGATTCTC AATGGAGTGCAGTGGTGCAATCTCGGCTCACTGCACCCTCTGCCTCCCAGGTTCAAAGGATTCTC T C HNRNPA2B1 Ensembl:ENSG00000122566 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1268253714 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16123740 32793 RMVar_ID_32793 Human_SNP_ID_314355161 A-to-I Human chr7 - 26183510 26183510 26183510 GACGGATCTCACTCTGGCCCAGAATGGAGTGCAGTGGTGCAATCTCGGCTCACTACACCCTCTGC GACGGATCTCACTCTGGCCCAGAATGGAGTGCCGTGGTGCAATCTCGGCTCACTACACCCTCTGC T G HNRNPA2B1 Ensembl:ENSG00000122566 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1409059531 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16123740,Human_RBP_ID_23075307 32794 RMVar_ID_32794 Human_SNP_ID_314360625 A-to-I Human chr7 + 26194157 26194156 26194157 GTGGCTCATGCCTGTAATCCCAGCACTTTGGGAAGGCCGAGGCGGACGGATCACGAGGTCAAGAG GTGGCTCATGCCTGTAATCCCAGCACTTTGGG_AGGCCGAGGCGGACGGATCACGAGGTCAAGAG GA G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1257930470 Functional Loss DEL dbSNP153 33..33 33 - - - 32795 RMVar_ID_32795 Human_SNP_ID_314366410 A-to-I Human chr7 + 26204889 26204889 26204889 TTGGCTCACCGCAACTTAAGCCTCCTGGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCCAAGTAGC TTGGCTCACCGCAACTTAAGCCTCCTGGGTTCGAGCAGTTCTCCTGCCTCAGCCTCCCAAGTAGC A G CBX3 Ensembl:ENSG00000122565 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1486785984 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59959,RMVar_hsa_circ_338573,RMVar_hsa_circ_62639 32796 RMVar_ID_32796 Human_SNP_ID_314366436 A-to-I Human chr7 + 26204972 26204972 26204972 CCACTATGCCTGGCTAATTTTGTATTTTTAGTAGAAACGGGGTTTCTCCATGTTGGTCAGGCTGG CCACTATGCCTGGCTAATTTTGTATTTTTAGTGGAAACGGGGTTTCTCCATGTTGGTCAGGCTGG A G CBX3 Ensembl:ENSG00000122565 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs191342675 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59959,RMVar_hsa_circ_338573,RMVar_hsa_circ_62639 32797 RMVar_ID_32797 Human_SNP_ID_314366466 A-to-I Human chr7 + 26205069 26205069 26205069 CCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGCCCCCGGCAATAGCATTTGCTT CCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCCCCCGGCAATAGCATTTGCTT A G CBX3 Ensembl:ENSG00000122565 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1288558705 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59959,RMVar_hsa_circ_338573,RMVar_hsa_circ_62639 32798 RMVar_ID_32798 Human_SNP_ID_314366799 A-to-I Human chr7 + 26206031 26206031 26206031 GAACTGCTTGAACCTGGGGAGGCGGAGGTTGCAGTGAGCTGAGATCACGCCACTGCACTCCAGCC GAACTGCTTGAACCTGGGGAGGCGGAGGTTGCGGTGAGCTGAGATCACGCCACTGCACTCCAGCC A G CBX3 Ensembl:ENSG00000122565 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1163562267 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59959,RMVar_hsa_circ_338573,RMVar_hsa_circ_62639 32799 RMVar_ID_32799 Human_SNP_ID_314367507 A-to-I Human chr7 + 26208009 26208009 26208009 AAGGCTGGAGGATCACTTGACACCAGGAATTCAAGACCAGCCTGGCCAACAAAATGAGACCCCTT AAGGCTGGAGGATCACTTGACACCAGGAATTCGAGACCAGCCTGGCCAACAAAATGAGACCCCTT A G CBX3 Ensembl:ENSG00000122565 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1384961349 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48144,RMVar_hsa_circ_338573,RMVar_hsa_circ_62639,RMVar_hsa_circ_105553,RMVar_hsa_circ_285734,RMVar_hsa_circ_244234,RMVar_hsa_circ_244235 32800 RMVar_ID_32800 Human_SNP_ID_314367574 A-to-I Human chr7 + 26208171 26208171 26208171 CTTGAGTCGGGAGTTGGAATCTTCAGTGAGCTATGATTCCACTACTGCACTCTCGTCTGGGCAAC CTTGAGTCGGGAGTTGGAATCTTCAGTGAGCTGTGATTCCACTACTGCACTCTCGTCTGGGCAAC A G CBX3 Ensembl:ENSG00000122565 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs530804358 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17577358 RMVar_hsa_circ_48144,RMVar_hsa_circ_338573,RMVar_hsa_circ_62639,RMVar_hsa_circ_105553,RMVar_hsa_circ_285734,RMVar_hsa_circ_244234,RMVar_hsa_circ_244235 32801 RMVar_ID_32801 Human_SNP_ID_314399586 A-to-I Human chr7 + 26331492 26331492 26331492 CCTGTAGCCCCTGCAACTTGAGGGGCTGTGGTAGGTGGATCACTTGGGCCTGGGAGGTCGAGGCT CCTGTAGCCCCTGCAACTTGAGGGGCTGTGGTGGGTGGATCACTTGGGCCTGGGAGGTCGAGGCT A G SNX10 Ensembl:ENSG00000086300 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1422868826 Functional Loss SNV dbSNP153 33..33 33 - - - 32802 RMVar_ID_32802 Human_SNP_ID_314417310 A-to-I Human chr7 + 26408247 26408247 26408247 TGGCCTCGTGATTCGTCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCTC TGGCCTCGTGATTCGTCCGCCTCGGCCTCCCAGAGTGCTGGGATTACAGGCGTGAGCCACTGCTC A G AC004540.1 Ensembl:ENSG00000214870 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs955741417 Functional Loss SNV dbSNP153 33..33 33 - - - 32803 RMVar_ID_32803 Human_SNP_ID_314479157 A-to-I Human chr7 - 26669003 26669003 26669003 GTACCAGAAGTATGACTCATGCAAAGCATTTTACCGTACAAATATCCTGGTGCGATGATGGGCCT GTACCAGAAGTATGACTCATGCAAAGCATTTTGCCGTACAAATATCCTGGTGCGATGATGGGCCT T C SKAP2 Ensembl:ENSG00000005020 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs532946023 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_681978,Human_RBP_ID_17312574,Human_RBP_ID_17425155,Human_RBP_ID_17540898 Human_miRNA_ID_839997,Human_miRNA_ID_2363890 RMVar_hsa_circ_107004,RMVar_hsa_circ_244236 32804 RMVar_ID_32804 Human_SNP_ID_314489792 A-to-I Human chr7 - 26719169 26719169 26719169 ATCTTAGATTTCTTTTTTTTCTTTTTAAAGATAGGGTCTTGCTCTGTTGCCCAGGCTGGAGTGCA ATCTTAGATTTCTTTTTTTTCTTTTTAAAGATGGGGTCTTGCTCTGTTGCCCAGGCTGGAGTGCA T C SKAP2 Ensembl:ENSG00000005020 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1447449092 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63158,RMVar_hsa_circ_361848,RMVar_hsa_circ_73362,RMVar_hsa_circ_295501,RMVar_hsa_circ_356106 32805 RMVar_ID_32805 Human_SNP_ID_314691225 A-to-I Human chr7 - 27535231 27535231 27535231 ATTTGTAAATGGCCAAAAAGCTTGTTCTTTGTATGTATCTATACTGTCTGGTTTTACATAAGAAC ATTTGTAAATGGCCAAAAAGCTTGTTCTTTGTGTGTATCTATACTGTCTGGTTTTACATAAGAAC T C HIBADH Ensembl:ENSG00000106049 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs73287946 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_302262,RMVar_hsa_circ_378984,RMVar_hsa_circ_355672 32806 RMVar_ID_32806 Human_SNP_ID_314759310 A-to-I Human chr7 + 27813448 27813448 27813448 GCCATCATGGCTTACTGTAGCCTTGACCTCCCAGACTCAGGTGATCCTCCCACCTCAGGTTTCTG GCCATCATGGCTTACTGTAGCCTTGACCTCCCGGACTCAGGTGATCCTCCCACCTCAGGTTTCTG A G TAX1BP1 Ensembl:ENSG00000106052 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1319972510 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16129531 RMVar_hsa_circ_43694,RMVar_hsa_circ_368257,RMVar_hsa_circ_99238,RMVar_hsa_circ_244263,RMVar_hsa_circ_244264,RMVar_hsa_circ_94189,RMVar_hsa_circ_70199,RMVar_hsa_circ_244268 32807 RMVar_ID_32807 Human_SNP_ID_314761295 A-to-I Human chr7 + 27822153 27822153 27822153 AAATTTGGGATGTTCAGCTGGCAAGCGTAATGAAGTATTACAAAATCTGAGAAAGTCTGAAATCT AAATTTGGGATGTTCAGCTGGCAAGCGTAATGGAGTATTACAAAATCTGAGAAAGTCTGAAATCT A G TAX1BP1 Ensembl:ENSG00000106052 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006191196 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43694,RMVar_hsa_circ_99238,RMVar_hsa_circ_244263,RMVar_hsa_circ_244264,RMVar_hsa_circ_94189,RMVar_hsa_circ_244268 32808 RMVar_ID_32808 Human_SNP_ID_314761303 A-to-I Human chr7 + 27822191 27822191 27822191 TACAAAATCTGAGAAAGTCTGAAATCTGAAACACTTCTGTTCCCAAGCATTTTGGATAAGGGGGA TACAAAATCTGAGAAAGTCTGAAATCTGAAACGCTTCTGTTCCCAAGCATTTTGGATAAGGGGGA A G TAX1BP1 Ensembl:ENSG00000106052 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1015327331 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43694,RMVar_hsa_circ_99238,RMVar_hsa_circ_244263,RMVar_hsa_circ_244264,RMVar_hsa_circ_94189,RMVar_hsa_circ_244268 32809 RMVar_ID_32809 Human_SNP_ID_314778976 A-to-I Human chr7 - 27891814 27891814 27891814 CTGTTTGAAACAGGGTCTTACTGTATCACTCTATCACCTAGGCTGGAGTGCAGTGATGCTATCAT CTGTTTGAAACAGGGTCTTACTGTATCACTCTGTCACCTAGGCTGGAGTGCAGTGATGCTATCAT T C JAZF1 Ensembl:ENSG00000153814 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1464745407 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67319 32810 RMVar_ID_32810 Human_SNP_ID_314858966 A-to-I Human chr7 + 28226977 28226977 28226977 TGGAGTGCAGTGGCGTGATCTCGGTTCACTGCAAGCTTCACCTCCCGGGTTCACGCCATTCTCCT TGGAGTGCAGTGGCGTGATCTCGGTTCACTGCGAGCTTCACCTCCCGGGTTCACGCCATTCTCCT A G JAZF1-AS1 Ensembl:ENSG00000234336 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1294633419 Functional Loss SNV dbSNP153 33..33 33 - - - 32811 RMVar_ID_32811 Human_SNP_ID_315104516 A-to-I Human chr7 + 29230575 29230575 29230575 GTTGGCCAGGCTGGTCTCGAACTCTTGTCCTTAAGTGATCTGCCTGCTTCAGCCTCTCAAAGTGC GTTGGCCAGGCTGGTCTCGAACTCTTGTCCTTTAGTGATCTGCCTGCTTCAGCCTCTCAAAGTGC A T AC004593.2,CHN2 Ensembl:ENSG00000285162,Ensembl:ENSG00000106069 Protein coding,Protein coding intron,intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs536345772 Functional Loss SNV dbSNP153 33..33 33 - - - 32812 RMVar_ID_32812 Human_SNP_ID_315109612 A-to-I Human chr7 + 29252258 29252258 29252258 TTGCCCAGGCCGGAGTGCAGTGGTGCCATCTCAGCTCACTGCAACCTCCACCTTCCAGGTTCACG TTGCCCAGGCCGGAGTGCAGTGGTGCCATCTCGGCTCACTGCAACCTCCACCTTCCAGGTTCACG A G AC004593.2,CHN2 Ensembl:ENSG00000285162,Ensembl:ENSG00000106069 Protein coding,Protein coding intron,intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1373758001 Functional Loss SNV dbSNP153 33..33 33 - - - 32813 RMVar_ID_32813 Human_SNP_ID_315148390 A-to-I Human chr7 + 29407924 29407924 29407924 AAAAAAATGCCCATGGCCGGGCTTGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGTGGCAGAG AAAAAAATGCCCATGGCCGGGCTTGGTGGCTCGTGCCTGTAATCCCAGCACTTTGGGTGGCAGAG A G AC004593.2,CHN2 Ensembl:ENSG00000285162,Ensembl:ENSG00000106069 Protein coding,Protein coding intron,intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs948856025 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_244293,RMVar_hsa_circ_377035 32814 RMVar_ID_32814 Human_SNP_ID_315151656 A-to-I Human chr7 + 29420927 29420927 29420927 TGCCCCCCAGGTTCAAGCGATTCTTCTGCCTCAGCCTCCTGAGTAGTTAGGATTATAGGCACCCA TGCCCCCCAGGTTCAAGCGATTCTTCTGCCTCGGCCTCCTGAGTAGTTAGGATTATAGGCACCCA A G AC004593.2,CHN2 Ensembl:ENSG00000285162,Ensembl:ENSG00000106069 Protein coding,Protein coding intron,intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs912298040 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_377035 32815 RMVar_ID_32815 Human_SNP_ID_315153216 A-to-I Human chr7 + 29427304 29427304 29427304 TGCCACTGCACTGCTAGCCTGGGTGATAGAGTAAGACTGTCTCAAAATAAATAAATAATAAAGGA TGCCACTGCACTGCTAGCCTGGGTGATAGAGTGAGACTGTCTCAAAATAAATAAATAATAAAGGA A G AC004593.2,CHN2 Ensembl:ENSG00000285162,Ensembl:ENSG00000106069 Protein coding,Protein coding intron,intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs932843045 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_377035 32816 RMVar_ID_32816 Human_SNP_ID_315153217 A-to-I Human chr7 + 29427304 29427304 29427304 TGCCACTGCACTGCTAGCCTGGGTGATAGAGTAAGACTGTCTCAAAATAAATAAATAATAAAGGA TGCCACTGCACTGCTAGCCTGGGTGATAGAGTTAGACTGTCTCAAAATAAATAAATAATAAAGGA A T AC004593.2,CHN2 Ensembl:ENSG00000285162,Ensembl:ENSG00000106069 Protein coding,Protein coding intron,intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs932843045 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_377035 32817 RMVar_ID_32817 Human_SNP_ID_315274086 A-to-I Human chr7 - 29938167 29938167 29938167 AAAATTAACTGGGCGTGGTGGTGCATGCCTGTAGTCCCAGCTACCAGGGAGGCTGAGGTGGGCGA AAAATTAACTGGGCGTGGTGGTGCATGCCTGTGGTCCCAGCTACCAGGGAGGCTGAGGTGGGCGA T C SCRN1 Ensembl:ENSG00000136193 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1201972558 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_244304,RMVar_hsa_circ_244305,RMVar_hsa_circ_342501,RMVar_hsa_circ_244307,RMVar_hsa_circ_51634,RMVar_hsa_circ_295340,RMVar_hsa_circ_318752,RMVar_hsa_circ_295319,RMVar_hsa_circ_244308 32818 RMVar_ID_32818 Human_SNP_ID_315276707 A-to-I Human chr7 - 29949644 29949644 29949644 GCCTGATGTGGTGGGTTATGCCCCATAATCTTAGCACTCTGGGAGGCCGAGGCAGGAGGATTGCT GCCTGATGTGGTGGGTTATGCCCCATAATCTTGGCACTCTGGGAGGCCGAGGCAGGAGGATTGCT T C SCRN1 Ensembl:ENSG00000136193 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1235508495 Functional Loss SNV dbSNP153 33..33 33 - - - 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 32819 RMVar_ID_32819 Human_SNP_ID_698938894 A-to-I Human chr22 + 20065445 20065445 20065445 CTCACTGCAACCTCCGCCTCCCAAGTTCAAGCAATTCTCCTGCCCCAGCCTCCTGATTAGCTGGG CTCACTGCAACCTCCGCCTCCCAAGTTCAAGCGATTCTCCTGCCCCAGCCTCCTGATTAGCTGGG A G TANGO2 Ensembl:ENSG00000183597 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1226320095 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122439,RMVar_hsa_circ_212990 32820 RMVar_ID_32820 Human_SNP_ID_698938918 A-to-I Human chr22 + 20065542 20065542 20065542 TTTTGTGTTTTTAGTAGAGACGGGGTTTCACCATGTTGGTCAGGCTGGTCTTGAACTCCTGACGT TTTTGTGTTTTTAGTAGAGACGGGGTTTCACCGTGTTGGTCAGGCTGGTCTTGAACTCCTGACGT A G TANGO2 Ensembl:ENSG00000183597 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs988252542 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122439,RMVar_hsa_circ_212990 32821 RMVar_ID_32821 Human_SNP_ID_698938919 A-to-I Human chr22 + 20065551 20065550 20065551 TTTAGTAGAGACGGGGTTTCACCATGTTGGTCAGGCTGGTCTTGAACTCCTGACGTGGTGATCCA TTTAGTAGAGACGGGGTTTCACCATGTTGGTC_GGCTGGTCTTGAACTCCTGACGTGGTGATCCA CA C TANGO2 Ensembl:ENSG00000183597 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs528653126 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_122439,RMVar_hsa_circ_212990 32822 RMVar_ID_32822 Human_SNP_ID_698938933 A-to-I Human chr22 + 20065601 20065601 20065601 TGACGTGGTGATCCACCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCACGC TGACGTGGTGATCCACCTGCCTCGGCCTCCCAGAGTGCTGGGATTACAGGCGTGAGCCACCACGC A G TANGO2 Ensembl:ENSG00000183597 Protein coding 3'UTR GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,29796672,31158229,31158229 RNA-Seq:(High) rs983537377 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8207775 RMVar_hsa_circ_122439,RMVar_hsa_circ_212990 32823 RMVar_ID_32823 Human_SNP_ID_698939368 A-to-I Human chr22 + 20067344 20067344 20067344 GCGAGGCTGAGGTGGGAGAATCGCTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCCAAGATTGCA GCGAGGCTGAGGTGGGAGAATCGCTTGAACCCGGGAGGCAGAGGTTGCAGTGAGCCAAGATTGCA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1416563597 Functional Loss SNV dbSNP153 33..33 33 - - - 32824 RMVar_ID_32824 Human_SNP_ID_698939372 A-to-I Human chr22 + 20067376 20067376 20067376 AGGAGGCAGAGGTTGCAGTGAGCCAAGATTGCACTACTGCACTCTGCCTGGGCAACAGAGGGAGA AGGAGGCAGAGGTTGCAGTGAGCCAAGATTGCGCTACTGCACTCTGCCTGGGCAACAGAGGGAGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1362391813 Functional Loss SNV dbSNP153 33..33 33 - - - 32825 RMVar_ID_32825 Human_SNP_ID_698939463 A-to-I Human chr22 + 20067740 20067739 20067740 AAAACCCTGTCTCTTAAAAAAAAAAAAAAAGGAAAAAGAAAGATTTGGACACGGACGGATACGCG AAAACCCTGTCTCTTAAAAAAAAAAAAAAAGG_AAAAGAAAGATTTGGACACGGACGGATACGCG GA G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs544706223 Functional Loss DEL dbSNP153 33..33 33 - - - 32826 RMVar_ID_32826 Human_SNP_ID_699038607 A-to-I Human chr22 + 20399689 20399689 20399689 ACCTCTTGGGTTCAAGCAATTCTCCTGACCTCAGGTGATCTGCCACCTTGGCCTCCCAAGTGCTG ACCTCTTGGGTTCAAGCAATTCTCCTGACCTCGGGTGATCTGCCACCTTGGCCTCCCAAGTGCTG A G ZNF74 Ensembl:ENSG00000185252 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1462053542 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25655782 Human_Splice_Rec_2139562,Human_Splice_Rec_2139563 RMVar_hsa_circ_213028,RMVar_hsa_circ_76347,RMVar_hsa_circ_376411,RMVar_hsa_circ_327312 32827 RMVar_ID_32827 Human_SNP_ID_699055840 A-to-I Human chr22 - 20462423 20462423 20462423 TTGAGTCCAGGAGTTTTAGACTTCGGTGAACTATGATCATGCCCCTGTACTGTAGCCTGGGCAAC TTGAGTCCAGGAGTTTTAGACTTCGGTGAACTGTGATCATGCCCCTGTACTGTAGCCTGGGCAAC T C KLHL22 Ensembl:ENSG00000099910 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1329117169 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_213033,RMVar_hsa_circ_345877,RMVar_hsa_circ_12450,RMVar_hsa_circ_276817,RMVar_hsa_circ_46747,RMVar_hsa_circ_213037 32828 RMVar_ID_32828 Human_SNP_ID_699063524 A-to-I Human chr22 - 20492754 20492754 20492754 AACCCCATTTCTGCTAAAAATGCAAGAAAATTAGCTGGGTGTGGTGGTGCACGCCTGTAATCCCA AACCCCATTTCTGCTAAAAATGCAAGAAAATTTGCTGGGTGTGGTGGTGCACGCCTGTAATCCCA T A KLHL22 Ensembl:ENSG00000099910 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs904800036 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23010979 32829 RMVar_ID_32829 Human_SNP_ID_699063529 A-to-I Human chr22 - 20492785 20492785 20492785 GAATGCGAGACCAGCCTGACCAACATGGTGAAACCCCATTTCTGCTAAAAATGCAAGAAAATTAG GAATGCGAGACCAGCCTGACCAACATGGTGAAGCCCCATTTCTGCTAAAAATGCAAGAAAATTAG T C KLHL22 Ensembl:ENSG00000099910 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1031373608 Functional Loss SNV dbSNP153 33..33 33 - - - 32830 RMVar_ID_32830 Human_SNP_ID_699064007 A-to-I Human chr22 - 20494545 20494545 20494545 GAAACCCCGTCTCTACTAAAAATACAAAAATTAGCTGGGTGTGGTGACACGTGCTTGTAATCCCA GAAACCCCGTCTCTACTAAAAATACAAAAATTCGCTGGGTGTGGTGACACGTGCTTGTAATCCCA T G KLHL22 Ensembl:ENSG00000099910 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1389205324 Functional Loss SNV dbSNP153 33..33 33 - - - 32831 RMVar_ID_32831 Human_SNP_ID_699064009 A-to-I Human chr22 - 20494554 20494554 20494554 CAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCTGGGTGTGGTGACACGTGCTT CAACATGGTGAAACCCCGTCTCTACTAAAAATGCAAAAATTAGCTGGGTGTGGTGACACGTGCTT T C KLHL22 Ensembl:ENSG00000099910 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1398082290 Functional Loss SNV dbSNP153 33..33 33 - - - 32832 RMVar_ID_32832 Human_SNP_ID_699064012 A-to-I Human chr22 - 20494563 20494563 20494563 TAGCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCTGGGTGTGGTGA TAGCCTGGCCAACATGGTGAAACCCCGTCTCTTCTAAAAATACAAAAATTAGCTGGGTGTGGTGA T A KLHL22 Ensembl:ENSG00000099910 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1048749652 Functional Loss SNV dbSNP153 33..33 33 - - - 32833 RMVar_ID_32833 Human_SNP_ID_699069456 A-to-I Human chr22 + 20513957 20513957 20513957 ATGATCTTGGCCCACTGCAACCTCTGGCTCCCAGGCTTAAGCGATCCTCCCACCTCAGCATTCCC ATGATCTTGGCCCACTGCAACCTCTGGCTCCCTGGCTTAAGCGATCCTCCCACCTCAGCATTCCC A T MED15 Ensembl:ENSG00000099917 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1450630783 Functional Loss SNV dbSNP153 33..33 33 - - - 32834 RMVar_ID_32834 Human_SNP_ID_699072824 A-to-I Human chr22 + 20527519 20527519 20527519 GCTGGAATGCAGTGATGTGTTCATGGCTCACTATGGCCTCGAACTCCTGGGCTCAAGTGATCCTC GCTGGAATGCAGTGATGTGTTCATGGCTCACTGTGGCCTCGAACTCCTGGGCTCAAGTGATCCTC A G MED15 Ensembl:ENSG00000099917 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1462138355 Functional Loss SNV dbSNP153 33..33 33 - - - 32835 RMVar_ID_32835 Human_SNP_ID_699075815 A-to-I Human chr22 + 20538524 20538524 20538524 CCCACGCCTTGCCCTCCCTAAATGCTGGGATTACAAGTGTGAGCCACCATGCCCAGCCTTCAACA CCCACGCCTTGCCCTCCCTAAATGCTGGGATTGCAAGTGTGAGCCACCATGCCCAGCCTTCAACA A G MED15 Ensembl:ENSG00000099917 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs769772079 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8148,RMVar_hsa_circ_309943,RMVar_hsa_circ_321131,RMVar_hsa_circ_265322 32836 RMVar_ID_32836 Human_SNP_ID_699076593 A-to-I Human chr22 + 20541561 20541561 20541561 GCTAGAGTGCAGTGGCACAATCTCGTCTCACTACAGCCTTCGCCTCCCAAATTCCGGTGATTTTC GCTAGAGTGCAGTGGCACAATCTCGTCTCACTGCAGCCTTCGCCTCCCAAATTCCGGTGATTTTC A G MED15 Ensembl:ENSG00000099917 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1033046788 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8148,RMVar_hsa_circ_309943,RMVar_hsa_circ_321131,RMVar_hsa_circ_265322 32837 RMVar_ID_32837 Human_SNP_ID_699085039 A-to-I Human chr22 + 20572888 20572888 20572888 TTGAGGCTGCAGTGAGCTGTGATGACAGCATTACACTCTAGCCTGGGAGACAGAGCAAAACTCTT TTGAGGCTGCAGTGAGCTGTGATGACAGCATTGCACTCTAGCCTGGGAGACAGAGCAAAACTCTT A G MED15 Ensembl:ENSG00000099917 Protein coding intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs568015230 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17572736,Human_RBP_ID_23311936,Human_RBP_ID_25656089 RMVar_hsa_circ_265322,RMVar_hsa_circ_53337,RMVar_hsa_circ_40848 32838 RMVar_ID_32838 Human_SNP_ID_699085108 A-to-I Human chr22 + 20573168 20573168 20573168 TTTTGTATTTTTAGTAGAGACGGGGTTTTGTCATGTTGGCCAGGCTGGTCTTGAACTCCTCGCCT TTTTGTATTTTTAGTAGAGACGGGGTTTTGTCGTGTTGGCCAGGCTGGTCTTGAACTCCTCGCCT A G MED15 Ensembl:ENSG00000099917 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs891802147 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265322,RMVar_hsa_circ_53337,RMVar_hsa_circ_40848 32839 RMVar_ID_32839 Human_SNP_ID_699085126 A-to-I Human chr22 + 20573229 20573229 20573229 GCCTTAAGAGATGTGCCCGCTTTGGCCTCCCAAAGTGCTGGAATTACAGGCGTAAGCCACTGTGC GCCTTAAGAGATGTGCCCGCTTTGGCCTCCCAGAGTGCTGGAATTACAGGCGTAAGCCACTGTGC A G MED15 Ensembl:ENSG00000099917 Protein coding intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1291272120 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17572738 RMVar_hsa_circ_265322,RMVar_hsa_circ_53337,RMVar_hsa_circ_40848 32840 RMVar_ID_32840 Human_SNP_ID_699129686 A-to-I Human chr22 - 20722236 20722236 20722236 GTTGCAGTGAGCTGAGATTGTACCACTGCACTACAGCCTGGGTGACAGACCGAGACTCTGTCTCA GTTGCAGTGAGCTGAGATTGTACCACTGCACTCCAGCCTGGGTGACAGACCGAGACTCTGTCTCA T G PI4KA Ensembl:ENSG00000241973 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1446757023 Functional Loss SNV dbSNP153 33..33 33 - - - 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_80854,RMVar_hsa_circ_213067,RMVar_hsa_circ_83593,RMVar_hsa_circ_121378,RMVar_hsa_circ_31708,RMVar_hsa_circ_213068,RMVar_hsa_circ_213069 32841 RMVar_ID_32841 Human_SNP_ID_699129934 A-to-I Human chr22 - 20723149 20723149 20723149 GCCAGGCTTGGTGGGCACCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCGTGAA GCCAGGCTTGGTGGGCACCTGTAGTCCCAGCTGCTCGGGAGGCTGAGGCAGGAGAATGGCGTGAA T C PI4KA Ensembl:ENSG00000241973 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1169789319 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_152566 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_80854,RMVar_hsa_circ_213067,RMVar_hsa_circ_83593,RMVar_hsa_circ_121378,RMVar_hsa_circ_31708,RMVar_hsa_circ_213068,RMVar_hsa_circ_213069 32842 RMVar_ID_32842 Human_SNP_ID_699130598 A-to-I Human chr22 - 20725690 20725690 20725690 AGTTTCGCTATGTTGTCCCAGGCTGGTCTCAAACTCCTGAGCTCAGGCAATCTGCCCACCTCCGC AGTTTCGCTATGTTGTCCCAGGCTGGTCTCAAGCTCCTGAGCTCAGGCAATCTGCCCACCTCCGC T C PI4KA Ensembl:ENSG00000241973 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1356135377 Functional Loss SNV dbSNP153 33..33 33 - - - 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_80854,RMVar_hsa_circ_213067,RMVar_hsa_circ_83593,RMVar_hsa_circ_121378,RMVar_hsa_circ_31708,RMVar_hsa_circ_213068,RMVar_hsa_circ_213069 32843 RMVar_ID_32843 Human_SNP_ID_699134631 A-to-I Human chr22 - 20739895 20739895 20739895 ATCATGCCTGGCTAATTTTTGTGTTTTTGTACAGACAGGGTTTCACCATGTTGGCCAGGCTGGTC ATCATGCCTGGCTAATTTTTGTGTTTTTGTACGGACAGGGTTTCACCATGTTGGCCAGGCTGGTC T C PI4KA Ensembl:ENSG00000241973 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1183596485 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14402492 RMVar_hsa_circ_98874,RMVar_hsa_circ_268629,RMVar_hsa_circ_84998,RMVar_hsa_circ_120195,RMVar_hsa_circ_213054,RMVar_hsa_circ_80886,RMVar_hsa_circ_213053,RMVar_hsa_circ_213055,RMVar_hsa_circ_127180,RMVar_hsa_circ_92859,RMVar_hsa_circ_213059,RMVar_hsa_circ_213060,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_80854,RMVar_hsa_circ_213067,RMVar_hsa_circ_83593,RMVar_hsa_circ_121378,RMVar_hsa_circ_213068,RMVar_hsa_circ_98385,RMVar_hsa_circ_8546,RMVar_hsa_circ_126937,RMVar_hsa_circ_213069,RMVar_hsa_circ_112078,RMVar_hsa_circ_213070,RMVar_hsa_circ_213072,RMVar_hsa_circ_94588,RMVar_hsa_circ_213073,RMVar_hsa_circ_213071,RMVar_hsa_circ_213074,RMVar_hsa_circ_96736,RMVar_hsa_circ_119222,RMVar_hsa_circ_213075,RMVar_hsa_circ_96897,RMVar_hsa_circ_124914,RMVar_hsa_circ_213080,RMVar_hsa_circ_76000,RMVar_hsa_circ_111158,RMVar_hsa_circ_213082,RMVar_hsa_circ_15166,RMVar_hsa_circ_213081,RMVar_hsa_circ_108128,RMVar_hsa_circ_87317,RMVar_hsa_circ_213083,RMVar_hsa_circ_213084,RMVar_hsa_circ_213085 32844 RMVar_ID_32844 Human_SNP_ID_699135551 A-to-I Human chr22 - 20743274 20743274 20743274 CAGGCGTGGTGGCGCATGCCTGTAATCCAGCTACTTGGGAGGCTGAGGTGGGAGGATCACTTGAA CAGGCGTGGTGGCGCATGCCTGTAATCCAGCTGCTTGGGAGGCTGAGGTGGGAGGATCACTTGAA T C PI4KA Ensembl:ENSG00000241973 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs536336937 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98874,RMVar_hsa_circ_268629,RMVar_hsa_circ_84998,RMVar_hsa_circ_120195,RMVar_hsa_circ_213054,RMVar_hsa_circ_80886,RMVar_hsa_circ_213053,RMVar_hsa_circ_213055,RMVar_hsa_circ_213060,RMVar_hsa_circ_265380,RMVar_hsa_circ_95529,RMVar_hsa_circ_100044,RMVar_hsa_circ_213064,RMVar_hsa_circ_213065,RMVar_hsa_circ_80854,RMVar_hsa_circ_213067,RMVar_hsa_circ_83593,RMVar_hsa_circ_121378,RMVar_hsa_circ_213068,RMVar_hsa_circ_98385,RMVar_hsa_circ_126937,RMVar_hsa_circ_213069,RMVar_hsa_circ_112078,RMVar_hsa_circ_213070,RMVar_hsa_circ_213072,RMVar_hsa_circ_94588,RMVar_hsa_circ_213073,RMVar_hsa_circ_213071,RMVar_hsa_circ_213074,RMVar_hsa_circ_96736,RMVar_hsa_circ_119222,RMVar_hsa_circ_213075,RMVar_hsa_circ_96897,RMVar_hsa_circ_124914,RMVar_hsa_circ_213080,RMVar_hsa_circ_76000,RMVar_hsa_circ_111158,RMVar_hsa_circ_213082,RMVar_hsa_circ_213081,RMVar_hsa_circ_108128,RMVar_hsa_circ_37192,RMVar_hsa_circ_97773,RMVar_hsa_circ_87317,RMVar_hsa_circ_213083,RMVar_hsa_circ_213084,RMVar_hsa_circ_213085,RMVar_hsa_circ_343635,RMVar_hsa_circ_118457,RMVar_hsa_circ_125982,RMVar_hsa_circ_103382,RMVar_hsa_circ_85564,RMVar_hsa_circ_91243,RMVar_hsa_circ_45048,RMVar_hsa_circ_118226,RMVar_hsa_circ_213088,RMVar_hsa_circ_213090,RMVar_hsa_circ_213091,RMVar_hsa_circ_213089,RMVar_hsa_circ_213086,RMVar_hsa_circ_213087,RMVar_hsa_circ_127522,RMVar_hsa_circ_96238,RMVar_hsa_circ_104929,RMVar_hsa_circ_213093,RMVar_hsa_circ_213095,RMVar_hsa_circ_213096,RMVar_hsa_circ_213094 32845 RMVar_ID_32845 Human_SNP_ID_699138574 A-to-I Human chr22 - 20754121 20754121 20754121 GATCTCACCATTGCACTCCAGACTGGGCAACAAAGTGAGACCCTGTCTCAAAAAAAATAGAAAAA GATCTCACCATTGCACTCCAGACTGGGCAACAGAGTGAGACCCTGTCTCAAAAAAAATAGAAAAA T C PI4KA Ensembl:ENSG00000241973 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs528897333 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98874,RMVar_hsa_circ_268629,RMVar_hsa_circ_84998,RMVar_hsa_circ_120195,RMVar_hsa_circ_213054,RMVar_hsa_circ_80886,RMVar_hsa_circ_213053,RMVar_hsa_circ_213055,RMVar_hsa_circ_213060,RMVar_hsa_circ_265380,RMVar_hsa_circ_95529,RMVar_hsa_circ_213065,RMVar_hsa_circ_80854,RMVar_hsa_circ_213067,RMVar_hsa_circ_83593,RMVar_hsa_circ_121378,RMVar_hsa_circ_213068,RMVar_hsa_circ_126937,RMVar_hsa_circ_213069,RMVar_hsa_circ_112078,RMVar_hsa_circ_213070,RMVar_hsa_circ_213073,RMVar_hsa_circ_213074,RMVar_hsa_circ_96736,RMVar_hsa_circ_119222,RMVar_hsa_circ_213075,RMVar_hsa_circ_96897,RMVar_hsa_circ_213080,RMVar_hsa_circ_76000,RMVar_hsa_circ_111158,RMVar_hsa_circ_213082,RMVar_hsa_circ_97773,RMVar_hsa_circ_213084,RMVar_hsa_circ_118457,RMVar_hsa_circ_125982,RMVar_hsa_circ_103382,RMVar_hsa_circ_85564,RMVar_hsa_circ_45048,RMVar_hsa_circ_34640,RMVar_hsa_circ_118226,RMVar_hsa_circ_213088,RMVar_hsa_circ_213090,RMVar_hsa_circ_213089,RMVar_hsa_circ_213086,RMVar_hsa_circ_213087,RMVar_hsa_circ_104929,RMVar_hsa_circ_213095,RMVar_hsa_circ_213096,RMVar_hsa_circ_94245,RMVar_hsa_circ_124016,RMVar_hsa_circ_213097,RMVar_hsa_circ_213098,RMVar_hsa_circ_13310,RMVar_hsa_circ_213099 32846 RMVar_ID_32846 Human_SNP_ID_699138704 A-to-I Human chr22 - 20754720 20754720 20754720 TGGTCTCGAACTCCTGACCTCGTGATCCACCCACCTCGGCCTCTCAAAGTGCTGGGATTATGGGC TGGTCTCGAACTCCTGACCTCGTGATCCACCCGCCTCGGCCTCTCAAAGTGCTGGGATTATGGGC T C PI4KA Ensembl:ENSG00000241973 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1209863868 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25656212 RMVar_hsa_circ_98874,RMVar_hsa_circ_268629,RMVar_hsa_circ_84998,RMVar_hsa_circ_120195,RMVar_hsa_circ_213054,RMVar_hsa_circ_80886,RMVar_hsa_circ_213053,RMVar_hsa_circ_213055,RMVar_hsa_circ_213060,RMVar_hsa_circ_265380,RMVar_hsa_circ_95529,RMVar_hsa_circ_213065,RMVar_hsa_circ_80854,RMVar_hsa_circ_213067,RMVar_hsa_circ_83593,RMVar_hsa_circ_121378,RMVar_hsa_circ_213068,RMVar_hsa_circ_126937,RMVar_hsa_circ_213069,RMVar_hsa_circ_112078,RMVar_hsa_circ_213070,RMVar_hsa_circ_213073,RMVar_hsa_circ_213074,RMVar_hsa_circ_96736,RMVar_hsa_circ_119222,RMVar_hsa_circ_213075,RMVar_hsa_circ_96897,RMVar_hsa_circ_213080,RMVar_hsa_circ_76000,RMVar_hsa_circ_111158,RMVar_hsa_circ_213082,RMVar_hsa_circ_97773,RMVar_hsa_circ_213084,RMVar_hsa_circ_118457,RMVar_hsa_circ_125982,RMVar_hsa_circ_103382,RMVar_hsa_circ_85564,RMVar_hsa_circ_45048,RMVar_hsa_circ_34640,RMVar_hsa_circ_118226,RMVar_hsa_circ_213088,RMVar_hsa_circ_213090,RMVar_hsa_circ_213089,RMVar_hsa_circ_213086,RMVar_hsa_circ_213087,RMVar_hsa_circ_104929,RMVar_hsa_circ_213095,RMVar_hsa_circ_213096,RMVar_hsa_circ_94245,RMVar_hsa_circ_124016,RMVar_hsa_circ_213097,RMVar_hsa_circ_213098,RMVar_hsa_circ_13310,RMVar_hsa_circ_213099 32847 RMVar_ID_32847 Human_SNP_ID_699138940 A-to-I Human chr22 - 20755555 20755555 20755555 CTCAAGTGATCCACCCGCCTCAGCCTCCCAAAATGCTGGGATTACAGGCATGAGCCACTGTGCCC CTCAAGTGATCCACCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGTGCCC T C PI4KA Ensembl:ENSG00000241973 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1002470851 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98874,RMVar_hsa_circ_268629,RMVar_hsa_circ_84998,RMVar_hsa_circ_120195,RMVar_hsa_circ_213054,RMVar_hsa_circ_80886,RMVar_hsa_circ_213053,RMVar_hsa_circ_213055,RMVar_hsa_circ_213060,RMVar_hsa_circ_265380,RMVar_hsa_circ_95529,RMVar_hsa_circ_213065,RMVar_hsa_circ_80854,RMVar_hsa_circ_213067,RMVar_hsa_circ_83593,RMVar_hsa_circ_121378,RMVar_hsa_circ_213068,RMVar_hsa_circ_126937,RMVar_hsa_circ_213069,RMVar_hsa_circ_112078,RMVar_hsa_circ_213070,RMVar_hsa_circ_213073,RMVar_hsa_circ_213074,RMVar_hsa_circ_96736,RMVar_hsa_circ_119222,RMVar_hsa_circ_213075,RMVar_hsa_circ_96897,RMVar_hsa_circ_213080,RMVar_hsa_circ_76000,RMVar_hsa_circ_111158,RMVar_hsa_circ_213082,RMVar_hsa_circ_97773,RMVar_hsa_circ_213084,RMVar_hsa_circ_118457,RMVar_hsa_circ_125982,RMVar_hsa_circ_103382,RMVar_hsa_circ_85564,RMVar_hsa_circ_45048,RMVar_hsa_circ_34640,RMVar_hsa_circ_118226,RMVar_hsa_circ_213088,RMVar_hsa_circ_213090,RMVar_hsa_circ_213089,RMVar_hsa_circ_213086,RMVar_hsa_circ_213087,RMVar_hsa_circ_104929,RMVar_hsa_circ_213095,RMVar_hsa_circ_213096,RMVar_hsa_circ_94245,RMVar_hsa_circ_124016,RMVar_hsa_circ_213097,RMVar_hsa_circ_213098,RMVar_hsa_circ_13310,RMVar_hsa_circ_213099 32848 RMVar_ID_32848 Human_SNP_ID_699139147 A-to-I Human chr22 - 20756272 20756272 20756272 ACCCGTCGGAGGTTGCAGTGAGCTGAGATCGCACCACTGCGCTCCAGCCTGGGCGATGAGCGAAA ACCCGTCGGAGGTTGCAGTGAGCTGAGATCGCCCCACTGCGCTCCAGCCTGGGCGATGAGCGAAA T G PI4KA Ensembl:ENSG00000241973 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1303752825 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25656217 RMVar_hsa_circ_98874,RMVar_hsa_circ_268629,RMVar_hsa_circ_84998,RMVar_hsa_circ_120195,RMVar_hsa_circ_213054,RMVar_hsa_circ_80886,RMVar_hsa_circ_213053,RMVar_hsa_circ_213055,RMVar_hsa_circ_213060,RMVar_hsa_circ_265380,RMVar_hsa_circ_95529,RMVar_hsa_circ_213065,RMVar_hsa_circ_80854,RMVar_hsa_circ_213067,RMVar_hsa_circ_83593,RMVar_hsa_circ_121378,RMVar_hsa_circ_213068,RMVar_hsa_circ_126937,RMVar_hsa_circ_213069,RMVar_hsa_circ_112078,RMVar_hsa_circ_213070,RMVar_hsa_circ_213073,RMVar_hsa_circ_213074,RMVar_hsa_circ_96736,RMVar_hsa_circ_119222,RMVar_hsa_circ_213075,RMVar_hsa_circ_96897,RMVar_hsa_circ_213080,RMVar_hsa_circ_76000,RMVar_hsa_circ_111158,RMVar_hsa_circ_213082,RMVar_hsa_circ_97773,RMVar_hsa_circ_213084,RMVar_hsa_circ_118457,RMVar_hsa_circ_125982,RMVar_hsa_circ_103382,RMVar_hsa_circ_85564,RMVar_hsa_circ_45048,RMVar_hsa_circ_34640,RMVar_hsa_circ_118226,RMVar_hsa_circ_213088,RMVar_hsa_circ_213090,RMVar_hsa_circ_213089,RMVar_hsa_circ_213086,RMVar_hsa_circ_213087,RMVar_hsa_circ_104929,RMVar_hsa_circ_213095,RMVar_hsa_circ_213096,RMVar_hsa_circ_94245,RMVar_hsa_circ_124016,RMVar_hsa_circ_213097,RMVar_hsa_circ_213098,RMVar_hsa_circ_13310,RMVar_hsa_circ_213099 32849 RMVar_ID_32849 Human_SNP_ID_699139663 A-to-I Human chr22 - 20758289 20758289 20758289 ACGATCTCAGCTGACTGCAAGCTCCGCCTCCCAGGTTCATGCCATTCTCCTGCCTCAGCCTCCCA ACGATCTCAGCTGACTGCAAGCTCCGCCTCCCGGGTTCATGCCATTCTCCTGCCTCAGCCTCCCA T C PI4KA Ensembl:ENSG00000241973 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1366004406 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98874,RMVar_hsa_circ_268629,RMVar_hsa_circ_84998,RMVar_hsa_circ_120195,RMVar_hsa_circ_213054,RMVar_hsa_circ_80886,RMVar_hsa_circ_213053,RMVar_hsa_circ_213055,RMVar_hsa_circ_213060,RMVar_hsa_circ_265380,RMVar_hsa_circ_95529,RMVar_hsa_circ_213065,RMVar_hsa_circ_80854,RMVar_hsa_circ_213067,RMVar_hsa_circ_83593,RMVar_hsa_circ_121378,RMVar_hsa_circ_213068,RMVar_hsa_circ_126937,RMVar_hsa_circ_213069,RMVar_hsa_circ_112078,RMVar_hsa_circ_213070,RMVar_hsa_circ_213073,RMVar_hsa_circ_213074,RMVar_hsa_circ_96736,RMVar_hsa_circ_119222,RMVar_hsa_circ_213075,RMVar_hsa_circ_96897,RMVar_hsa_circ_213080,RMVar_hsa_circ_76000,RMVar_hsa_circ_111158,RMVar_hsa_circ_213082,RMVar_hsa_circ_97773,RMVar_hsa_circ_213084,RMVar_hsa_circ_118457,RMVar_hsa_circ_125982,RMVar_hsa_circ_103382,RMVar_hsa_circ_85564,RMVar_hsa_circ_45048,RMVar_hsa_circ_34640,RMVar_hsa_circ_118226,RMVar_hsa_circ_213088,RMVar_hsa_circ_213090,RMVar_hsa_circ_213089,RMVar_hsa_circ_213086,RMVar_hsa_circ_213087,RMVar_hsa_circ_104929,RMVar_hsa_circ_213095,RMVar_hsa_circ_213096,RMVar_hsa_circ_94245,RMVar_hsa_circ_124016,RMVar_hsa_circ_213097,RMVar_hsa_circ_213098,RMVar_hsa_circ_13310,RMVar_hsa_circ_213099 32850 RMVar_ID_32850 Human_SNP_ID_699156965 A-to-I Human chr22 - 20822251 20822251 20822251 CTTGAGCCCGGGAATTTGAGACTAGCTTGGGCAGCATAGCAAAACCTATCCCTACAAAAATAAAA CTTGAGCCCGGGAATTTGAGACTAGCTTGGGCGGCATAGCAAAACCTATCCCTACAAAAATAAAA T C PI4KA Ensembl:ENSG00000241973 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1009426725 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96897,RMVar_hsa_circ_213080,RMVar_hsa_circ_118457,RMVar_hsa_circ_213086,RMVar_hsa_circ_124016,RMVar_hsa_circ_213097,RMVar_hsa_circ_42819,RMVar_hsa_circ_120791,RMVar_hsa_circ_213104,RMVar_hsa_circ_275242,RMVar_hsa_circ_368634,RMVar_hsa_circ_213109,RMVar_hsa_circ_92402,RMVar_hsa_circ_213112,RMVar_hsa_circ_323711,RMVar_hsa_circ_269194,RMVar_hsa_circ_295707,RMVar_hsa_circ_213118,RMVar_hsa_circ_301966,RMVar_hsa_circ_328014,RMVar_hsa_circ_279295,RMVar_hsa_circ_213119,RMVar_hsa_circ_213120,RMVar_hsa_circ_377075,RMVar_hsa_circ_213122,RMVar_hsa_circ_91401,RMVar_hsa_circ_213121 32851 RMVar_ID_32851 Human_SNP_ID_699167514 A-to-I Human chr22 + 20860819 20860819 20860819 TCTGTAATCCCAACAATTTGTAAGGCTGAGGTAGGCAGATCATTTTAGCCCAGGAGTTTGAGACC TCTGTAATCCCAACAATTTGTAAGGCTGAGGTTGGCAGATCATTTTAGCCCAGGAGTTTGAGACC A T SNAP29 Ensembl:ENSG00000099940 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1413151616 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112623,RMVar_hsa_circ_213126 32852 RMVar_ID_32852 Human_SNP_ID_699175694 A-to-I Human chr22 + 20891037 20891028 20891038 GCGGAGCTTGCAGTGAGCCAAGGCGACAGAGCAAGACTCTGTCTCAAAAAATAAAAAATAGTGCA GCGGAGCTTGCAGTGAGCCAAGGC__________GACTCTGTCTCAAAAAATAAAAAATAGTGCA CGACAGAGCAA C SNAP29 Ensembl:ENSG00000099940 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1210192900 Functional Loss DEL dbSNP153 25..34 33 - - - RMVar_hsa_circ_112623,RMVar_hsa_circ_213126 32853 RMVar_ID_32853 Human_SNP_ID_699184386 A-to-I Human chr22 + 20922125 20922125 20922125 ACCTCTGCCTCCCAGGTTCAAGTGATTCTCCTACCTCAGCCTCCTGAGTAGCTGGGACTGCATGG ACCTCTGCCTCCCAGGTTCAAGTGATTCTCCTCCCTCAGCCTCCTGAGTAGCTGGGACTGCATGG A C CRKL Ensembl:ENSG00000099942 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904630944 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95421,RMVar_hsa_circ_213129 32854 RMVar_ID_32854 Human_SNP_ID_699184387 A-to-I Human chr22 + 20922125 20922125 20922125 ACCTCTGCCTCCCAGGTTCAAGTGATTCTCCTACCTCAGCCTCCTGAGTAGCTGGGACTGCATGG ACCTCTGCCTCCCAGGTTCAAGTGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTGCATGG A G CRKL Ensembl:ENSG00000099942 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904630944 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95421,RMVar_hsa_circ_213129 32855 RMVar_ID_32855 Human_SNP_ID_699185851 A-to-I Human chr22 + 20927290 20927290 20927290 TCGGTTCACTGCAGTCTCCACCTCCCGGGTTCAAGTGATTCTCCTGCCTCAGTCTCCTGAGTAGC TCGGTTCACTGCAGTCTCCACCTCCCGGGTTCGAGTGATTCTCCTGCCTCAGTCTCCTGAGTAGC A G CRKL Ensembl:ENSG00000099942 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1428329299 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95421,RMVar_hsa_circ_213129 32856 RMVar_ID_32856 Human_SNP_ID_699209216 A-to-I Human chr22 + 21002718 21002718 21002718 TGGAGTGCAGTGGCGCGATCTCGGCTCACTGCAAACTCCGCCTCCCGGGTTCACGCCATTCGGCT TGGAGTGCAGTGGCGCGATCTCGGCTCACTGCGAACTCCGCCTCCCGGGTTCACGCCATTCGGCT A G THAP7-AS1 Ensembl:ENSG00000230513 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1452790228 Functional Loss SNV dbSNP153 33..33 33 - - - 32857 RMVar_ID_32857 Human_SNP_ID_699210379 A-to-I Human chr22 - 21005765 21005765 21005765 TTGGTAGACACAGGGTTTCACCATGTTGGCTAAGCTGGTCTCGAGCTCCTGAACTCAAGTGATCC TTGGTAGACACAGGGTTTCACCATGTTGGCTAGGCTGGTCTCGAGCTCCTGAACTCAAGTGATCC T C AC002472.2 Ensembl:ENSG00000284060 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1304867611 Functional Loss SNV dbSNP153 33..33 33 - - - 32858 RMVar_ID_32858 Human_SNP_ID_699219468 A-to-I Human chr22 + 21036048 21036048 21036048 TGGCTCACTGTAGCCTCTGCCTTCAGGATTCAAACGATTCTCATGTCTCAGCCTCCCGAATGGCT TGGCTCACTGTAGCCTCTGCCTTCAGGATTCAGACGATTCTCATGTCTCAGCCTCCCGAATGGCT A G AC002472.1 Ensembl:ENSG00000226872 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs370640058 Functional Loss SNV dbSNP153 33..33 33 - - - 32859 RMVar_ID_32859 Human_SNP_ID_699328452 A-to-I Human chr22 + 21584881 21584881 21584881 TACTCAGGAGGCTGAGGCATAAGAAGCACTTGAGCCTGGGAGGCGGAGGTTGGAGTGAGCTGAGA TACTCAGGAGGCTGAGGCATAAGAAGCACTTGGGCCTGGGAGGCGGAGGTTGGAGTGAGCTGAGA A G UBE2L3 Ensembl:ENSG00000185651 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1265646083 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77446,RMVar_hsa_circ_213150 32860 RMVar_ID_32860 Human_SNP_ID_699334367 A-to-I Human chr22 + 21607539 21607539 21607539 TCCGTCTTAAAAAAAAAAAAAAAAAAAAAAAGATTGTTCTTGGGCTCTCTGTGAAGCTTGGATTT TCCGTCTTAAAAAAAAAAAAAAAAAAAAAAAGGTTGTTCTTGGGCTCTCTGTGAAGCTTGGATTT A G UBE2L3 Ensembl:ENSG00000185651 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167373997 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14406366 RMVar_hsa_circ_94365,RMVar_hsa_circ_77446,RMVar_hsa_circ_213150,RMVar_hsa_circ_335608,RMVar_hsa_circ_213151 32861 RMVar_ID_32861 Human_SNP_ID_699345922 A-to-I Human chr22 + 21647306 21647306 21647306 TTTTCTAGAGACAGGGTTTTGCCATGTTGCTCACACTTGTCTCGAACTCCTGGACTCAAGTGATC TTTTCTAGAGACAGGGTTTTGCCATGTTGCTCTCACTTGTCTCGAACTCCTGGACTCAAGTGATC A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1192288833 Functional Loss SNV dbSNP153 33..33 33 - - - 32862 RMVar_ID_32862 Human_SNP_ID_699345935 A-to-I Human chr22 + 21647371 21647370 21647372 TGCTCACCTCAGCCTGCCAAAGTGCTGGGATTACAGGCTTGCACCACCACGCCTGGCCTCAGTTG TGCTCACCTCAGCCTGCCAAAGTGCTGGGATT__AGGCTTGCACCACCACGCCTGGCCTCAGTTG TAC T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1300398051 Functional Loss DEL dbSNP153 33..34 33 - - - 32863 RMVar_ID_32863 Human_SNP_ID_699354777 A-to-I Human chr22 + 21678839 21678839 21678839 GCTTCGACCTTCCAGGACCAAGTGCTCCTTCCACCTCAGTCTCCCAAGTAGATGGGACCACAGGC GCTTCGACCTTCCAGGACCAAGTGCTCCTTCCCCCTCAGTCTCCCAAGTAGATGGGACCACAGGC A C PPIL2 Ensembl:ENSG00000100023 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934034677 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17004,RMVar_hsa_circ_267588 32864 RMVar_ID_32864 Human_SNP_ID_699354904 A-to-I Human chr22 + 21679247 21679247 21679247 TTATTTTTGTAGAGATGAGGTTTCCCTATGTCACCCAGGCTGGTCTTGAAGTCCTGGGCTCAAGT TTATTTTTGTAGAGATGAGGTTTCCCTATGTCGCCCAGGCTGGTCTTGAAGTCCTGGGCTCAAGT A G PPIL2 Ensembl:ENSG00000100023 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992772244 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17572742 RMVar_hsa_circ_17004,RMVar_hsa_circ_267588 32865 RMVar_ID_32865 Human_SNP_ID_699358525 A-to-I Human chr22 + 21691423 21691423 21691423 CAGGAGGAGGCCAGGCGCGGTGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCCGAGGCAGGC CAGGAGGAGGCCAGGCGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGC A G PPIL2 Ensembl:ENSG00000100023 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1022432665 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267588,RMVar_hsa_circ_340989 32866 RMVar_ID_32866 Human_SNP_ID_699359263 A-to-I Human chr22 + 21692867 21692867 21692867 ACTATGACATGAACCTGGGAGGCGGAGCTTGCAGTGAACCGACATCGCGCCACTGCACTCCAGCC ACTATGACATGAACCTGGGAGGCGGAGCTTGCGGTGAACCGACATCGCGCCACTGCACTCCAGCC A G PPIL2 Ensembl:ENSG00000100023 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1197545599 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267588,RMVar_hsa_circ_340989 32867 RMVar_ID_32867 Human_SNP_ID_699359355 A-to-I Human chr22 + 21693193 21693193 21693193 CCTTGGCCTCCTAAGTAGTTGGGACTACAGGCACACGCCACCACGCCCAGCTAATTTTTGTATTT CCTTGGCCTCCTAAGTAGTTGGGACTACAGGCGCACGCCACCACGCCCAGCTAATTTTTGTATTT A G PPIL2 Ensembl:ENSG00000100023 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1414922638 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267588,RMVar_hsa_circ_340989 32868 RMVar_ID_32868 Human_SNP_ID_699383982 A-to-I Human chr22 - 21782909 21782909 21782909 AGAAAACTGACTGGGTGCAGTGGCGCATGCCTATAATCCGAGCACTTTGGGAGGCTGAGGCGGGA AGAAAACTGACTGGGTGCAGTGGCGCATGCCTGTAATCCGAGCACTTTGGGAGGCTGAGGCGGGA T C MAPK1 Ensembl:ENSG00000100030 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs897925111 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_293631,RMVar_hsa_circ_338062,RMVar_hsa_circ_272945,RMVar_hsa_circ_213180,RMVar_hsa_circ_213176,RMVar_hsa_circ_213177,RMVar_hsa_circ_213178,RMVar_hsa_circ_278881,RMVar_hsa_circ_288512,RMVar_hsa_circ_36667,RMVar_hsa_circ_213179 32869 RMVar_ID_32869 Human_SNP_ID_699383983 A-to-I Human chr22 - 21782909 21782909 21782909 AGAAAACTGACTGGGTGCAGTGGCGCATGCCTATAATCCGAGCACTTTGGGAGGCTGAGGCGGGA AGAAAACTGACTGGGTGCAGTGGCGCATGCCTCTAATCCGAGCACTTTGGGAGGCTGAGGCGGGA T G MAPK1 Ensembl:ENSG00000100030 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs897925111 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_293631,RMVar_hsa_circ_338062,RMVar_hsa_circ_272945,RMVar_hsa_circ_213180,RMVar_hsa_circ_213176,RMVar_hsa_circ_213177,RMVar_hsa_circ_213178,RMVar_hsa_circ_278881,RMVar_hsa_circ_288512,RMVar_hsa_circ_36667,RMVar_hsa_circ_213179 32870 RMVar_ID_32870 Human_SNP_ID_699384173 A-to-I Human chr22 - 21783505 21783505 21783505 ACTGGTCTTGAATTCCTGGGCTCAAGCAATCTACCCTCCTTGGCCTCCCAAAATGTTGGAATTAC ACTGGTCTTGAATTCCTGGGCTCAAGCAATCTTCCCTCCTTGGCCTCCCAAAATGTTGGAATTAC T A MAPK1 Ensembl:ENSG00000100030 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1480844656 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_293631,RMVar_hsa_circ_338062,RMVar_hsa_circ_272945,RMVar_hsa_circ_213180,RMVar_hsa_circ_213176,RMVar_hsa_circ_213177,RMVar_hsa_circ_213178,RMVar_hsa_circ_278881,RMVar_hsa_circ_288512,RMVar_hsa_circ_36667,RMVar_hsa_circ_213179 32871 RMVar_ID_32871 Human_SNP_ID_699387312 A-to-I Human chr22 - 21794000 21794000 21794000 GGCTCACTGCGACCTCTGCCTCCCGGGTTCAAATGATTCTCCGGCCTCGCCTCCCGTGTAGCTGA GGCTCACTGCGACCTCTGCCTCCCGGGTTCAATTGATTCTCCGGCCTCGCCTCCCGTGTAGCTGA T A MAPK1 Ensembl:ENSG00000100030 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs977050837 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29660,RMVar_hsa_circ_293631,RMVar_hsa_circ_338062,RMVar_hsa_circ_213180,RMVar_hsa_circ_213177,RMVar_hsa_circ_213178,RMVar_hsa_circ_288512,RMVar_hsa_circ_36667,RMVar_hsa_circ_306894,RMVar_hsa_circ_300591,RMVar_hsa_circ_213181,RMVar_hsa_circ_213183,RMVar_hsa_circ_213182,RMVar_hsa_circ_213185 32872 RMVar_ID_32872 Human_SNP_ID_699387771 A-to-I Human chr22 - 21795506 21795506 21795506 CAGAGGTTGCAGTGAGGCAAGGTCACACCACTATACTCCAGCCTGGGTGGCAGAGTGAGACTCTG CAGAGGTTGCAGTGAGGCAAGGTCACACCACTGTACTCCAGCCTGGGTGGCAGAGTGAGACTCTG T C MAPK1 Ensembl:ENSG00000100030 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1361985534 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14408800,Human_RBP_ID_17572676,Human_RBP_ID_25657073 RMVar_hsa_circ_29660,RMVar_hsa_circ_293631,RMVar_hsa_circ_338062,RMVar_hsa_circ_213180,RMVar_hsa_circ_213177,RMVar_hsa_circ_213178,RMVar_hsa_circ_288512,RMVar_hsa_circ_36667,RMVar_hsa_circ_306894,RMVar_hsa_circ_300591,RMVar_hsa_circ_213181,RMVar_hsa_circ_213183,RMVar_hsa_circ_213182,RMVar_hsa_circ_213185 32873 RMVar_ID_32873 Human_SNP_ID_699387774 A-to-I Human chr22 - 21795519 21795519 21795519 TGAACCCGGGAGGCAGAGGTTGCAGTGAGGCAAGGTCACACCACTATACTCCAGCCTGGGTGGCA TGAACCCGGGAGGCAGAGGTTGCAGTGAGGCAGGGTCACACCACTATACTCCAGCCTGGGTGGCA T C MAPK1 Ensembl:ENSG00000100030 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs538804164 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17572676 RMVar_hsa_circ_29660,RMVar_hsa_circ_293631,RMVar_hsa_circ_338062,RMVar_hsa_circ_213180,RMVar_hsa_circ_213177,RMVar_hsa_circ_213178,RMVar_hsa_circ_288512,RMVar_hsa_circ_36667,RMVar_hsa_circ_306894,RMVar_hsa_circ_300591,RMVar_hsa_circ_213181,RMVar_hsa_circ_213183,RMVar_hsa_circ_213182,RMVar_hsa_circ_213185 32874 RMVar_ID_32874 Human_SNP_ID_699389989 A-to-I Human chr22 - 21803884 21803884 21803884 GTGGTGGCATGTGCCTGTGGTCCCAGCTACTCAGGAGGCTGAGTGGGAGGACTGCTTGAGCCTGG GTGGTGGCATGTGCCTGTGGTCCCAGCTACTCGGGAGGCTGAGTGGGAGGACTGCTTGAGCCTGG T C MAPK1 Ensembl:ENSG00000100030 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs576755968 Functional Loss SNV dbSNP153 33..33 33 - - - 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 32875 RMVar_ID_32875 Human_SNP_ID_699400023 A-to-I Human chr22 - 21840195 21840195 21840195 AGAATTGCTTGAGCCTAGGTCAAGGCTATAGTAACCTGTGACCACGCGACTGCACTCTATCCTGG AGAATTGCTTGAGCCTAGGTCAAGGCTATAGTTACCTGTGACCACGCGACTGCACTCTATCCTGG T A MAPK1 Ensembl:ENSG00000100030 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474413219 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_213189 32876 RMVar_ID_32876 Human_SNP_ID_699400024 A-to-I Human chr22 - 21840200 21840200 21840200 GCAGGAGAATTGCTTGAGCCTAGGTCAAGGCTATAGTAACCTGTGACCACGCGACTGCACTCTAT GCAGGAGAATTGCTTGAGCCTAGGTCAAGGCTGTAGTAACCTGTGACCACGCGACTGCACTCTAT T C MAPK1 Ensembl:ENSG00000100030 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs908359578 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_213189 32877 RMVar_ID_32877 Human_SNP_ID_699516240 A-to-I Human chr22 - 22275971 22275971 22275971 GCTGGACTCGAACTCCTGACCTCAGGTGATCCACCCACCATGGCCTCCCAAAGTGCTGGGATTAC GCTGGACTCGAACTCCTGACCTCAGGTGATCCGCCCACCATGGCCTCCCAAAGTGCTGGGATTAC T C lnc-ZNF280B-6 RNACentral:URS0000D5AEA8 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1206050459 Functional Loss SNV dbSNP153 33..33 33 - - - 32878 RMVar_ID_32878 Human_SNP_ID_699530552 A-to-I Human chr22 + 22322799 22322799 22322799 AATTATGTATCCTGGTACCAGCAGCTCCCAGGAACAGCCCCCAAACTCCTCATTTATGACAATAA AATTATGTATCCTGGTACCAGCAGCTCCCAGGCACAGCCCCCAAACTCCTCATTTATGACAATAA A C IGLV1-51,AC245060.7 Ensembl:ENSG00000211644,Ensembl:ENSG00000286129 Other,lincRNA CDS,exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs564976360 Functional Loss SNV dbSNP153 33..33 33 - - - 32879 RMVar_ID_32879 Human_SNP_ID_699530553 A-to-I Human chr22 + 22322799 22322799 22322799 AATTATGTATCCTGGTACCAGCAGCTCCCAGGAACAGCCCCCAAACTCCTCATTTATGACAATAA AATTATGTATCCTGGTACCAGCAGCTCCCAGGGACAGCCCCCAAACTCCTCATTTATGACAATAA A G IGLV1-51,AC245060.7 Ensembl:ENSG00000211644,Ensembl:ENSG00000286129 Other,lincRNA CDS,exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs564976360 Functional Loss SNV dbSNP153 33..33 33 - - - 32880 RMVar_ID_32880 Human_SNP_ID_699530554 A-to-I Human chr22 + 22322799 22322799 22322799 AATTATGTATCCTGGTACCAGCAGCTCCCAGGAACAGCCCCCAAACTCCTCATTTATGACAATAA AATTATGTATCCTGGTACCAGCAGCTCCCAGGTACAGCCCCCAAACTCCTCATTTATGACAATAA A T IGLV1-51,AC245060.7 Ensembl:ENSG00000211644,Ensembl:ENSG00000286129 Other,lincRNA CDS,exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs564976360 Functional Loss SNV dbSNP153 33..33 33 - - - 32881 RMVar_ID_32881 Human_SNP_ID_699530559 A-to-I Human chr22 + 22322802 22322802 22322802 TATGTATCCTGGTACCAGCAGCTCCCAGGAACAGCCCCCAAACTCCTCATTTATGACAATAATAA TATGTATCCTGGTACCAGCAGCTCCCAGGAACGGCCCCCAAACTCCTCATTTATGACAATAATAA A G IGLV1-51,AC245060.7 Ensembl:ENSG00000211644,Ensembl:ENSG00000286129 Other,lincRNA CDS,exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs760387463 Functional Loss SNV dbSNP153 33..33 33 - - - 32882 RMVar_ID_32882 Human_SNP_ID_699530560 A-to-I Human chr22 + 22322802 22322802 22322802 TATGTATCCTGGTACCAGCAGCTCCCAGGAACAGCCCCCAAACTCCTCATTTATGACAATAATAA TATGTATCCTGGTACCAGCAGCTCCCAGGAACTGCCCCCAAACTCCTCATTTATGACAATAATAA A T IGLV1-51,AC245060.7 Ensembl:ENSG00000211644,Ensembl:ENSG00000286129 Other,lincRNA CDS,exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs760387463 Functional Loss SNV dbSNP153 33..33 33 - - - 32883 RMVar_ID_32883 Human_SNP_ID_699776252 A-to-I Human chr22 + 23200821 23200821 23200821 GGCTCAAGCGATCCACCCGCCTTGGCCTCCCAAAGTGCTGGGACTCCAGGCATGAGCCACCATGC GGCTCAAGCGATCCACCCGCCTTGGCCTCCCAGAGTGCTGGGACTCCAGGCATGAGCCACCATGC A G BCR Ensembl:ENSG00000186716 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1379253988 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266517 32884 RMVar_ID_32884 Human_SNP_ID_699888950 A-to-I Human chr22 - 23618989 23618989 23618989 TTTTGAAGATTTAGTAGAGACGTGGTTTTACCATGTTGGCCAGGATGGTCTCGATCTCTTGACCT TTTTGAAGATTTAGTAGAGACGTGGTTTTACCTTGTTGGCCAGGATGGTCTCGATCTCTTGACCT T A DRICH1 Ensembl:ENSG00000189269 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924770373 Functional Loss SNV dbSNP153 33..33 33 - - - 32885 RMVar_ID_32885 Human_SNP_ID_699888951 A-to-I Human chr22 - 23618989 23618989 23618989 TTTTGAAGATTTAGTAGAGACGTGGTTTTACCATGTTGGCCAGGATGGTCTCGATCTCTTGACCT TTTTGAAGATTTAGTAGAGACGTGGTTTTACCGTGTTGGCCAGGATGGTCTCGATCTCTTGACCT T C DRICH1 Ensembl:ENSG00000189269 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924770373 Functional Loss SNV dbSNP153 33..33 33 - - - 32886 RMVar_ID_32886 Human_SNP_ID_699896035 A-to-I Human chr22 - 23644969 23644969 23644969 TGCCTCCTGGGTTCAAGCGATTCTCTTGCCTCAGCCTCCCGAGTAGCTGGGGTTACAGGCACCTG TGCCTCCTGGGTTCAAGCGATTCTCTTGCCTCGGCCTCCCGAGTAGCTGGGGTTACAGGCACCTG T C GUSBP11 Ensembl:ENSG00000228315 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs529858851 Functional Loss SNV dbSNP153 33..33 33 - - - 32887 RMVar_ID_32887 Human_SNP_ID_699896190 A-to-I Human chr22 - 23645579 23645579 23645579 TGGTGTGGTGGCGCGTGCCTGTAATCCCAGCTACTCAGAAGGCTGAGGCAGGAGAATCGCTTGAA TGGTGTGGTGGCGCGTGCCTGTAATCCCAGCTGCTCAGAAGGCTGAGGCAGGAGAATCGCTTGAA T C GUSBP11 Ensembl:ENSG00000228315 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1396288410 Functional Loss SNV dbSNP153 33..33 33 - - - 32888 RMVar_ID_32888 Human_SNP_ID_699896324 A-to-I Human chr22 - 23646094 23646094 23646094 TATTAGGCCAGGGACAGTGGTTTATGCCTGTAATCCCAGCACTTTGGGAAGCCAAGACAGGCAGA TATTAGGCCAGGGACAGTGGTTTATGCCTGTAGTCCCAGCACTTTGGGAAGCCAAGACAGGCAGA T C GUSBP11 Ensembl:ENSG00000228315 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1179953009 Functional Loss SNV dbSNP153 33..33 33 - - - 32889 RMVar_ID_32889 Human_SNP_ID_699896571 A-to-I Human chr22 - 23646933 23646933 23646933 TCACTGCAACCTTTCCCTCCCAGATTCAAGCAATTCTTCCACCTCAGCCTCCTGAGCAGCTGGGA TCACTGCAACCTTTCCCTCCCAGATTCAAGCAGTTCTTCCACCTCAGCCTCCTGAGCAGCTGGGA T C GUSBP11 Ensembl:ENSG00000228315 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1569104724 Functional Loss SNV dbSNP153 33..33 33 - - - 32890 RMVar_ID_32890 Human_SNP_ID_699896574 A-to-I Human chr22 - 23646944 23646944 23646944 GTGATTTTGGCTCACTGCAACCTTTCCCTCCCAGATTCAAGCAATTCTTCCACCTCAGCCTCCTG GTGATTTTGGCTCACTGCAACCTTTCCCTCCCTGATTCAAGCAATTCTTCCACCTCAGCCTCCTG T A GUSBP11 Ensembl:ENSG00000228315 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1177078861 Functional Loss SNV dbSNP153 33..33 33 - - - 32891 RMVar_ID_32891 Human_SNP_ID_699896672 A-to-I Human chr22 - 23647343 23647343 23647343 GCCTGACCTTACATGTTTTTTTAAGTGAAGCAAGGTCTCACTGTATTGCCCAGGCTAGTCTTGAA GCCTGACCTTACATGTTTTTTTAAGTGAAGCAGGGTCTCACTGTATTGCCCAGGCTAGTCTTGAA T C GUSBP11 Ensembl:ENSG00000228315 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1344803900 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5249922,Human_RBP_ID_14412953 32892 RMVar_ID_32892 Human_SNP_ID_699896840 A-to-I Human chr22 - 23647902 23647902 23647902 TTCGGAGGCTAAGGTGGGAAGATCCTGAGGTCAGAAGTGTGAGACTAGCCTGGGCAACATAGTGA TTCGGAGGCTAAGGTGGGAAGATCCTGAGGTCCGAAGTGTGAGACTAGCCTGGGCAACATAGTGA T G GUSBP11 Ensembl:ENSG00000228315 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1399638284 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8262841,Human_RBP_ID_14412960 32893 RMVar_ID_32893 Human_SNP_ID_699896907 A-to-I Human chr22 - 23648162 23648162 23648162 AACTCAGGAGGCTGAGGCAGGAGAGTCGCTTGAACTCAGTGGTCGGAGGTTGCAGTGAGCCGAGA AACTCAGGAGGCTGAGGCAGGAGAGTCGCTTGGACTCAGTGGTCGGAGGTTGCAGTGAGCCGAGA T C GUSBP11 Ensembl:ENSG00000228315 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1001668116 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14412975 32894 RMVar_ID_32894 Human_SNP_ID_699897183 A-to-I Human chr22 - 23648855 23648855 23648855 TTTGCGCCTAGGAATTGAGACTGCGGTGAGCTATGATCACACCCCTGCATTCCAGCCTGGACAAC TTTGCGCCTAGGAATTGAGACTGCGGTGAGCTGTGATCACACCCCTGCATTCCAGCCTGGACAAC T C GUSBP11 Ensembl:ENSG00000228315 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs980064397 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14412983,Human_RBP_ID_22267358 32895 RMVar_ID_32895 Human_SNP_ID_699897653 A-to-I Human chr22 - 23650592 23650592 23650592 CCTGTAATCCCAGCTACTTGGGAAGCTGAGGCAGGAGAATCTTGAACCTGGGAGACGGAGGTTGC CCTGTAATCCCAGCTACTTGGGAAGCTGAGGCGGGAGAATCTTGAACCTGGGAGACGGAGGTTGC T C GUSBP11,ASLP1 Ensembl:ENSG00000228315,Ensembl:ENSG00000244723 lincRNA,Pseudogene intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1028400619 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14413018,Human_RBP_ID_17400493,Human_RBP_ID_18516481,Human_RBP_ID_18535413,Human_RBP_ID_25657834 32896 RMVar_ID_32896 Human_SNP_ID_699898010 A-to-I Human chr22 - 23652036 23652036 23652036 ACAACTGCTTGAACCCAGGAAGCAGAGGTTGCAGTGAGCTAAGATTGAGCCACTGCCAGCCTGGG ACAACTGCTTGAACCCAGGAAGCAGAGGTTGCGGTGAGCTAAGATTGAGCCACTGCCAGCCTGGG T C GUSBP11,ASLP1 Ensembl:ENSG00000228315,Ensembl:ENSG00000244723 lincRNA,Pseudogene intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947245186 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18516624 32897 RMVar_ID_32897 Human_SNP_ID_699898020 A-to-I Human chr22 - 23652088 23652088 23652088 AGGTGTGGTGGTGGGCGCCTGTAATCCAATCTACTCAGGAGACTGAGGCAGGACAACTGCTTGAA AGGTGTGGTGGTGGGCGCCTGTAATCCAATCTGCTCAGGAGACTGAGGCAGGACAACTGCTTGAA T C GUSBP11,ASLP1 Ensembl:ENSG00000228315,Ensembl:ENSG00000244723 lincRNA,Pseudogene intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs902887396 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14413050,Human_RBP_ID_18516624 32898 RMVar_ID_32898 Human_SNP_ID_699898419 A-to-I Human chr22 - 23653571 23653571 23653571 GGGAGGCGGAGGTTGCAGTGAGCCGAGGTTGCACTACTGCAGTCCAGCCTGGCTCTGTCTTGGTG GGGAGGCGGAGGTTGCAGTGAGCCGAGGTTGCGCTACTGCAGTCCAGCCTGGCTCTGTCTTGGTG T C GUSBP11 Ensembl:ENSG00000228315 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs950094197 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3679464,Human_RBP_ID_5101752 RMVar_hsa_circ_213273,RMVar_hsa_circ_93202 32899 RMVar_ID_32899 Human_SNP_ID_699898947 A-to-I Human chr22 - 23655639 23655639 23655639 CGCCACTGCGCCTGGCTAATTTTTGTATTTTCAGTAAAGACAGGGTTTCCCCATGTTGGCCGGGC CGCCACTGCGCCTGGCTAATTTTTGTATTTTCGGTAAAGACAGGGTTTCCCCATGTTGGCCGGGC T C GUSBP11 Ensembl:ENSG00000228315 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1445873118 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_213273,RMVar_hsa_circ_93202 32900 RMVar_ID_32900 Human_SNP_ID_699898949 A-to-I Human chr22 - 23655653 23655653 23655653 GGACTATAGCTGCCCGCCACTGCGCCTGGCTAATTTTTGTATTTTCAGTAAAGACAGGGTTTCCC GGACTATAGCTGCCCGCCACTGCGCCTGGCTAGTTTTTGTATTTTCAGTAAAGACAGGGTTTCCC T C GUSBP11 Ensembl:ENSG00000228315 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054245205 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_213273,RMVar_hsa_circ_93202 32901 RMVar_ID_32901 Human_SNP_ID_699898981 A-to-I Human chr22 - 23655763 23655763 23655763 ATGTCTTGCTCTGTCACCCAGGCTGGAGTGCAATGGTGCCATCTCTGTTCACTGCAACCTCCACC ATGTCTTGCTCTGTCACCCAGGCTGGAGTGCAGTGGTGCCATCTCTGTTCACTGCAACCTCCACC T C GUSBP11 Ensembl:ENSG00000228315 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs186321874 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_213273,RMVar_hsa_circ_93202 32902 RMVar_ID_32902 Human_SNP_ID_699898992 A-to-I Human chr22 - 23655797 23655794 23655797 GCTATCACATAGGTACTGTATTATTTTTCAGAAGATGTCTTGCTCTGTCACCCAGGCTGGAGTGC GCTATCACATAGGTACTGTATTATTTTTCAGA___TGTCTTGCTCTGTCACCCAGGCTGGAGTGC ATCT A GUSBP11 Ensembl:ENSG00000228315 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs998774500 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_14413142 RMVar_hsa_circ_213273,RMVar_hsa_circ_93202 32903 RMVar_ID_32903 Human_SNP_ID_699899254 A-to-I Human chr22 - 23656864 23656864 23656864 CCTGGCCAACATGGTGAAACCACATCTCTACTAAAAATAGAAAAATTATCCTGGCGTGGTGGCAA CCTGGCCAACATGGTGAAACCACATCTCTACTTAAAATAGAAAAATTATCCTGGCGTGGTGGCAA T A GUSBP11 Ensembl:ENSG00000228315 lincRNA intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1302667889 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_213273,RMVar_hsa_circ_93202 32904 RMVar_ID_32904 Human_SNP_ID_699900013 A-to-I Human chr22 - 23658525 23658525 23658525 ATCCCAGTTACTCGGAAGGCTAAGGCATGAGAATCGCTTGAACCCGGGAGGTGGAGGTTGCGGTG ATCCCAGTTACTCGGAAGGCTAAGGCATGAGATTCGCTTGAACCCGGGAGGTGGAGGTTGCGGTG T A GUSBP11,AP000347.1 Ensembl:ENSG00000228315,Ensembl:ENSG00000272578 lincRNA,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1020420529 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14413204,Human_RBP_ID_17400515,Human_RBP_ID_18516628,Human_RBP_ID_27033422 RMVar_hsa_circ_213273,RMVar_hsa_circ_93202 32905 RMVar_ID_32905 Human_SNP_ID_699921545 A-to-I Human chr22 - 23739653 23739653 23739653 CGGAGGTTGCAGTGAGCCAAGATTGTGCCACTACCCTTCAGCCTGGGTGACAGGGCAAGACTCCA CGGAGGTTGCAGTGAGCCAAGATTGTGCCACTTCCCTTCAGCCTGGGTGACAGGGCAAGACTCCA T A ZNF70 Ensembl:ENSG00000187792 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1235800443 Functional Loss SNV dbSNP153 33..33 33 - - - 32906 RMVar_ID_32906 Human_SNP_ID_699921769 A-to-I Human chr22 - 23740504 23740504 23740504 TGCCTGCCTTGGCCTCCTGAAGTGTTGGGATTACAGGCGTGAGCCATGTGCCCAGCCAGCTTATT TGCCTGCCTTGGCCTCCTGAAGTGTTGGGATTGCAGGCGTGAGCCATGTGCCCAGCCAGCTTATT T C ZNF70 Ensembl:ENSG00000187792 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1325290139 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19031848 32907 RMVar_ID_32907 Human_SNP_ID_699922212 A-to-I Human chr22 - 23742214 23742214 23742214 GAGATGGAGTGTTGCCCTGTTGCCAGGCTGGAATGCAGTGGCGTGATCTTGGCTTACTGCAAGCT GAGATGGAGTGTTGCCCTGTTGCCAGGCTGGAGTGCAGTGGCGTGATCTTGGCTTACTGCAAGCT T C ZNF70 Ensembl:ENSG00000187792 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs766972191 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14414385 32908 RMVar_ID_32908 Human_SNP_ID_699923269 A-to-I Human chr22 - 23745765 23745765 23745765 TTGTTGCTGTTGTTGTTGTTGTTGTTTGAGATAGAGTCTCGCTTTGTTGCCCACGTTGGAGTGCA TTGTTGCTGTTGTTGTTGTTGTTGTTTGAGATGGAGTCTCGCTTTGTTGCCCACGTTGGAGTGCA T C ZNF70 Ensembl:ENSG00000187792 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1284943525 Functional Loss SNV dbSNP153 33..33 33 - - - 32909 RMVar_ID_32909 Human_SNP_ID_699935083 A-to-I Human chr22 - 23785959 23785959 23785959 TGTGAGCCACTGCGCCCGGCCTTGTAATCCCAACTCTTTAGGAGGCCAAGGCAGGGAGGATCACT TGTGAGCCACTGCGCCCGGCCTTGTAATCCCAGCTCTTTAGGAGGCCAAGGCAGGGAGGATCACT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1296907354 Functional Loss SNV dbSNP153 33..33 33 - - - 32910 RMVar_ID_32910 Human_SNP_ID_699937909 A-to-I Human chr22 + 23795808 23795808 23795808 TGTGCTGGAGGTGCTTTTTTTTTTTTTTTTTGAGATGGAGTTTTCACTCTTGTTGCCCAGGCTGG TGTGCTGGAGGTGCTTTTTTTTTTTTTTTTTGGGATGGAGTTTTCACTCTTGTTGCCCAGGCTGG A G SMARCB1 Ensembl:ENSG00000099956 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1387477380 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42186,RMVar_hsa_circ_318921,RMVar_hsa_circ_349182,RMVar_hsa_circ_55884,RMVar_hsa_circ_213291,RMVar_hsa_circ_213292,RMVar_hsa_circ_101800,RMVar_hsa_circ_213293 32911 RMVar_ID_32911 Human_SNP_ID_699937910 A-to-I Human chr22 + 23795808 23795808 23795808 TGTGCTGGAGGTGCTTTTTTTTTTTTTTTTTGAGATGGAGTTTTCACTCTTGTTGCCCAGGCTGG TGTGCTGGAGGTGCTTTTTTTTTTTTTTTTTGTGATGGAGTTTTCACTCTTGTTGCCCAGGCTGG A T SMARCB1 Ensembl:ENSG00000099956 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1387477380 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42186,RMVar_hsa_circ_318921,RMVar_hsa_circ_349182,RMVar_hsa_circ_55884,RMVar_hsa_circ_213291,RMVar_hsa_circ_213292,RMVar_hsa_circ_101800,RMVar_hsa_circ_213293 32912 RMVar_ID_32912 Human_SNP_ID_699958168 A-to-I Human chr22 + 23866181 23866181 23866181 ACAGAGGGAGACACTATCTTTAAAAAAAAAAAAAGAAAGAAAAAAGGAAAAAAGAGCTTAGAAAA ACAGAGGGAGACACTATCTTTAAAAAAAAAAAGAGAAAGAAAAAAGGAAAAAAGAGCTTAGAAAA A G AP000350.4,SLC2A11 Ensembl:ENSG00000251357,Ensembl:ENSG00000133460 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs545052939 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_376864 32913 RMVar_ID_32913 Human_SNP_ID_699958169 A-to-I Human chr22 + 23866181 23866181 23866183 ACAGAGGGAGACACTATCTTTAAAAAAAAAAAAAGAAAGAAAAAAGGAAAAAAGAGCTTAGAAAA ACAGAGGGAGACACTATCTTTAAAAAAAAAAAGAAAAAGAAAAAAGGAAAAAAGAGCTTAGAAAA AAG GAA AP000350.4,SLC2A11 Ensembl:ENSG00000251357,Ensembl:ENSG00000133460 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs796433700 Functional Loss MNV dbSNP153 33..35 33 - - - RMVar_hsa_circ_376864 32914 RMVar_ID_32914 Human_SNP_ID_699958175 A-to-I Human chr22 + 23866185 23866183 23866186 AGGGAGACACTATCTTTAAAAAAAAAAAAAGAAAGAAAAAAGGAAAAAAGAGCTTAGAAAACTCT AGGGAGACACTATCTTTAAAAAAAAAAAAAG___GAAAAAAGGAAAAAAGAGCTTAGAAAACTCT GAAA G AP000350.4,SLC2A11 Ensembl:ENSG00000251357,Ensembl:ENSG00000133460 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1568986848 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_376864 32915 RMVar_ID_32915 Human_SNP_ID_699958176 A-to-I Human chr22 + 23866185 23866183 23866185 AGGGAGACACTATCTTTAAAAAAAAAAAAAGAAAGAAAAAAGGAAAAAAGAGCTTAGAAAACTCT AGGGAGACACTATCTTTAAAAAAAAAAAAAG__AGAAAAAAGGAAAAAAGAGCTTAGAAAACTCT GAA G AP000350.4,SLC2A11 Ensembl:ENSG00000251357,Ensembl:ENSG00000133460 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs397965250 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_376864 32916 RMVar_ID_32916 Human_SNP_ID_699958177 A-to-I Human chr22 + 23866185 23866183 23866185 AGGGAGACACTATCTTTAAAAAAAAAAAAAGAAAGAAAAAAGGAAAAAAGAGCTTAGAAAACTCT AGGGAGACACTATCTTTAAAAAAAAAAAAAGA_AGAAAAAAGGAAAAAAGAGCTTAGAAAACTCT GAA GA AP000350.4,SLC2A11 Ensembl:ENSG00000251357,Ensembl:ENSG00000133460 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs397965250 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_376864 32917 RMVar_ID_32917 Human_SNP_ID_699964007 A-to-I Human chr22 + 23887148 23887148 23887148 ACCTCTGCCTCCTGGACTCAAGCGATCCTCCCACCTCAGCCCCCCAAGTAGGTGGGACCACAGGC ACCTCTGCCTCCTGGACTCAAGCGATCCTCCCCCCTCAGCCCCCCAAGTAGGTGGGACCACAGGC A C AP000350.4 Ensembl:ENSG00000251357 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1427364230 Functional Loss SNV dbSNP153 33..33 33 - - - 32918 RMVar_ID_32918 Human_SNP_ID_700002395 A-to-I Human chr22 + 24042026 24042026 24042026 CATGCTGGAGTGCAGTGGCACAATCAGGGCTCACTGCAGCCTCGACTTCCCAGGCTCAAACGATC CATGCTGGAGTGCAGTGGCACAATCAGGGCTCGCTGCAGCCTCGACTTCCCAGGCTCAAACGATC A G CABIN1 Ensembl:ENSG00000099991 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1452293601 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2833,RMVar_hsa_circ_352275,RMVar_hsa_circ_273863,RMVar_hsa_circ_45410,RMVar_hsa_circ_45618,RMVar_hsa_circ_73395 32919 RMVar_ID_32919 Human_SNP_ID_700004097 A-to-I Human chr22 + 24048521 24048521 24048521 CAGCTCACTGCAGCCTCTACCTCCTGGGCTCAAACGATTCTCCCACATCAGCCTCCTGAGTAGCT CAGCTCACTGCAGCCTCTACCTCCTGGGCTCAGACGATTCTCCCACATCAGCCTCCTGAGTAGCT A G CABIN1 Ensembl:ENSG00000099991 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1381592309 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2833,RMVar_hsa_circ_352275,RMVar_hsa_circ_45410,RMVar_hsa_circ_5056,RMVar_hsa_circ_373359,RMVar_hsa_circ_24002,RMVar_hsa_circ_213306 32920 RMVar_ID_32920 Human_SNP_ID_700019361 A-to-I Human chr22 + 24109337 24109337 24109337 GCCTCAACCTCCTGGGCTCAAGTGATCCTCCCACCTCAGCCTCCCAAGTAACTGCCACGCCTGCC GCCTCAACCTCCTGGGCTCAAGTGATCCTCCCCCCTCAGCCTCCCAAGTAACTGCCACGCCTGCC A C CABIN1 Ensembl:ENSG00000099991 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs980163663 Functional Loss SNV dbSNP153 33..33 33 - - - 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 32921 RMVar_ID_32921 Human_SNP_ID_700019506 A-to-I Human chr22 + 24110103 24110103 24110103 TGAGGCAGGAGGATTGCTTGAACCTGGGAGGTAGAGGTTGCAGTGAGCCAAGATCGTGCAATTGC TGAGGCAGGAGGATTGCTTGAACCTGGGAGGTGGAGGTTGCAGTGAGCCAAGATCGTGCAATTGC A G CABIN1 Ensembl:ENSG00000099991 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1345278445 Functional Loss SNV dbSNP153 33..33 33 - - - 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 32922 RMVar_ID_32922 Human_SNP_ID_700035326 A-to-I Human chr22 + 24174241 24174224 24174242 CTTCAACCTCCCTGGGCTCAGGTGATCCTCCTACCTCAGCCTCCCAAGTAGCTGAGACTACAAGC CTTCAACCTCCCTGGG__________________CTCAGCCTCCCAAGTAGCTGAGACTACAAGC GCTCAGGTGATCCTCCTAC G CABIN1 Ensembl:ENSG00000099991 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1168521791 Functional Loss DEL dbSNP153 17..34 33 - - - RMVar_hsa_circ_88015,RMVar_hsa_circ_98366,RMVar_hsa_circ_213313,RMVar_hsa_circ_213314 32923 RMVar_ID_32923 Human_SNP_ID_700035354 A-to-I Human chr22 + 24174338 24174338 24174338 TTTTGTAGAGATGGGGTTTCACCATGTTGCCCAAGCTGGTCTTAAACTCCTGGGCTCAGGAGATC TTTTGTAGAGATGGGGTTTCACCATGTTGCCCCAGCTGGTCTTAAACTCCTGGGCTCAGGAGATC A C CABIN1 Ensembl:ENSG00000099991 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1412610460 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88015,RMVar_hsa_circ_98366,RMVar_hsa_circ_213313,RMVar_hsa_circ_213314 32924 RMVar_ID_32924 Human_SNP_ID_700035365 A-to-I Human chr22 + 24174381 24174381 24174381 AAACTCCTGGGCTCAGGAGATCCACTCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAA AAACTCCTGGGCTCAGGAGATCCACTCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAA A G CABIN1 Ensembl:ENSG00000099991 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs1281282313 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88015,RMVar_hsa_circ_98366,RMVar_hsa_circ_213313,RMVar_hsa_circ_213314 32925 RMVar_ID_32925 Human_SNP_ID_700065473 A-to-I Human chr22 + 24273858 24273854 24273858 TCCGCTCACCGCAACCTACGCCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGG TCCGCTCACCGCAACCTACGCCTCCCAGG____AGCGATTCTCCTGCCTCAGCCTCCCAAGTAGG GTTCA G SPECC1L,SPECC1L-ADORA2A Ensembl:ENSG00000100014,Ensembl:ENSG00000258555 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs781245049 Functional Loss DEL dbSNP153 30..33 33 - - - 32926 RMVar_ID_32926 Human_SNP_ID_700090581 A-to-I Human chr22 + 24370803 24370803 24370803 TACAACACGATGCACACTGAAGACATTGTGCTAAATGAAACAAGCCATATACAAAAGGGCTAATA TACAACACGATGCACACTGAAGACATTGTGCTGAATGAAACAAGCCATATACAAAAGGGCTAATA A G SPECC1L,SPECC1L-ADORA2A Ensembl:ENSG00000100014,Ensembl:ENSG00000258555 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs529996596 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114427,RMVar_hsa_circ_213316 32927 RMVar_ID_32927 Human_SNP_ID_700092307 A-to-I Human chr22 + 24377141 24377141 24377141 TCCTCTGTGACTGGCTTCTTTCACTTAGCATCATGTTTTTAAGGTTCATCCATGCTGTAGCATAT TCCTCTGTGACTGGCTTCTTTCACTTAGCATCGTGTTTTTAAGGTTCATCCATGCTGTAGCATAT A G SPECC1L,SPECC1L-ADORA2A Ensembl:ENSG00000100014,Ensembl:ENSG00000258555 Protein coding,Protein coding intron,intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs988971645 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114427,RMVar_hsa_circ_213316 32928 RMVar_ID_32928 Human_SNP_ID_700093317 A-to-I Human chr22 + 24381741 24381741 24381741 GCCAGCTCTACTAAAAATACAAAAAATTAGCCAGGCGTGGTGGCAGGCGCCTGTAGTCCCAGCTA GCCAGCTCTACTAAAAATACAAAAAATTAGCCGGGCGTGGTGGCAGGCGCCTGTAGTCCCAGCTA A G SPECC1L,SPECC1L-ADORA2A Ensembl:ENSG00000100014,Ensembl:ENSG00000258555 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1294289572 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114427,RMVar_hsa_circ_213316 32929 RMVar_ID_32929 Human_SNP_ID_700093320 A-to-I Human chr22 + 24381753 24381753 24381753 AAAAATACAAAAAATTAGCCAGGCGTGGTGGCAGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTA AAAAATACAAAAAATTAGCCAGGCGTGGTGGCGGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTA A G SPECC1L,SPECC1L-ADORA2A Ensembl:ENSG00000100014,Ensembl:ENSG00000258555 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1205754891 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114427,RMVar_hsa_circ_213316 32930 RMVar_ID_32930 Human_SNP_ID_700094160 A-to-I Human chr22 + 24384953 24384950 24384953 AAAAAATTAGGTGGGCACCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATGGCTGAAC AAAAAATTAGGTGGGCACCTGTAGTCCCAG___CTTGGGAGGCTGAGGCAGGAGAATGGCTGAAC GCTA G SPECC1L,SPECC1L-ADORA2A Ensembl:ENSG00000100014,Ensembl:ENSG00000258555 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1392658185 Functional Loss DEL dbSNP153 31..33 33 - - - RMVar_hsa_circ_114427,RMVar_hsa_circ_213316 32931 RMVar_ID_32931 Human_SNP_ID_700094162 A-to-I Human chr22 + 24384953 24384953 24384953 AAAAAATTAGGTGGGCACCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATGGCTGAAC AAAAAATTAGGTGGGCACCTGTAGTCCCAGCTGCTTGGGAGGCTGAGGCAGGAGAATGGCTGAAC A G SPECC1L,SPECC1L-ADORA2A Ensembl:ENSG00000100014,Ensembl:ENSG00000258555 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1373907518 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114427,RMVar_hsa_circ_213316 32932 RMVar_ID_32932 Human_SNP_ID_700100197 A-to-I Human chr22 + 24409526 24409526 24409526 TAAAATACTCTGGGCCAGGTAAGGTGGATCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGT TAAAATACTCTGGGCCAGGTAAGGTGGATCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGT A G SPECC1L,SPECC1L-ADORA2A Ensembl:ENSG00000100014,Ensembl:ENSG00000258555 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1420263310 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114427,RMVar_hsa_circ_213316 32933 RMVar_ID_32933 Human_SNP_ID_700142129 A-to-I Human chr22 + 24570885 24570885 24570885 TCACCCAGGCTGCAGTGCGGTGGCTTGATCTCAGCTCACTGCCACCTCCTCCAACTCCCAGGTTC TCACCCAGGCTGCAGTGCGGTGGCTTGATCTCCGCTCACTGCCACCTCCTCCAACTCCCAGGTTC A C SNRPD3,GGT1 Ensembl:ENSG00000100028,Ensembl:ENSG00000286070 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1043010182 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105930,RMVar_hsa_circ_110278,RMVar_hsa_circ_213352,RMVar_hsa_circ_342398,RMVar_hsa_circ_213355 32934 RMVar_ID_32934 Human_SNP_ID_700142162 A-to-I Human chr22 + 24571019 24571019 24571019 TTTTGTGTGTTCAGTAGAGAAGGGGTTTTGCCATGTTGGCCAGTCTGGTCTCAAACTTATGACCT TTTTGTGTGTTCAGTAGAGAAGGGGTTTTGCCGTGTTGGCCAGTCTGGTCTCAAACTTATGACCT A G SNRPD3,GGT1 Ensembl:ENSG00000100028,Ensembl:ENSG00000286070 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs888483330 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105930,RMVar_hsa_circ_110278,RMVar_hsa_circ_213352,RMVar_hsa_circ_342398,RMVar_hsa_circ_213355 32935 RMVar_ID_32935 Human_SNP_ID_700142521 A-to-I Human chr22 + 24572507 24572507 24572507 TTCAGGGGCTGGGTGCGGCGGCTCACGCATGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGCGG TTCAGGGGCTGGGTGCGGCGGCTCACGCATGTCATCCCAGCACTTTGGGAGGCCAAGGCGGGCGG A C SNRPD3,GGT1 Ensembl:ENSG00000100028,Ensembl:ENSG00000286070 Protein coding,Protein coding 3'UTR,intron GSE38233;GSE100210;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 24183664,29129909,30559470 RNA-Seq:(High) rs945921831 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1943735,Human_miRNA_ID_1946771,Human_miRNA_ID_2087371,Human_miRNA_ID_2117926,Human_miRNA_ID_2201509,Human_miRNA_ID_2204574,Human_miRNA_ID_2317111,Human_miRNA_ID_2320265,Human_miRNA_ID_2323419,Human_miRNA_ID_2326594,Human_miRNA_ID_2329681,Human_miRNA_ID_2520972,Human_miRNA_ID_2524138,Human_miRNA_ID_2775994,Human_miRNA_ID_2817020,Human_miRNA_ID_2823320,Human_miRNA_ID_2829451,Human_miRNA_ID_2832607,Human_miRNA_ID_2836735,Human_miRNA_ID_2842083,Human_miRNA_ID_2847143,Human_miRNA_ID_2850169,Human_miRNA_ID_2864285,Human_miRNA_ID_3114021 RMVar_hsa_circ_105930,RMVar_hsa_circ_110278,RMVar_hsa_circ_213352,RMVar_hsa_circ_213355,RMVar_hsa_circ_213356,RMVar_hsa_circ_120154 32936 RMVar_ID_32936 Human_SNP_ID_700142555 A-to-I Human chr22 + 24572605 24572605 24572605 CAATATGGTGAAACCTCGTGTGTACTAAAAATAAAAAAATTAGCCGGGTGCGGTGGCATGTACCT CAATATGGTGAAACCTCGTGTGTACTAAAAATTAAAAAATTAGCCGGGTGCGGTGGCATGTACCT A T SNRPD3,GGT1 Ensembl:ENSG00000100028,Ensembl:ENSG00000286070 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs12172173 Functional Loss SNV dbSNP153 33..33 33 - - - 32937 RMVar_ID_32937 Human_SNP_ID_700142564 A-to-I Human chr22 + 24572634 24572634 24572634 AATAAAAAAATTAGCCGGGTGCGGTGGCATGTACCTGTAGTCCCAGCTACTCGGGAGGCTGAGGC AATAAAAAAATTAGCCGGGTGCGGTGGCATGTTCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGC A T SNRPD3,GGT1 Ensembl:ENSG00000100028,Ensembl:ENSG00000286070 Protein coding,Protein coding 3'UTR,intron GSE99789;GSE107867 esophageal squamous carcinoma cells,EC109;ASD brains,cerebellum - 29796672,30559470 RNA-Seq:(High) rs1225173442 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_276562 32938 RMVar_ID_32938 Human_SNP_ID_700142565 A-to-I Human chr22 + 24572646 24572646 24572646 AGCCGGGTGCGGTGGCATGTACCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGAAGATTCGCT AGCCGGGTGCGGTGGCATGTACCTGTAGTCCCGGCTACTCGGGAGGCTGAGGCAGAAGATTCGCT A G SNRPD3,GGT1 Ensembl:ENSG00000100028,Ensembl:ENSG00000286070 Protein coding,Protein coding 3'UTR,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1137756 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1359430 32939 RMVar_ID_32939 Human_SNP_ID_700142651 A-to-I Human chr22 + 24573002 24573002 24573002 GCTGAGGTAGAGGATTGTTTGAGAGGAGTTCAAAACCAGCCCGCGAGACATAGTGAGACCCTGTC GCTGAGGTAGAGGATTGTTTGAGAGGAGTTCAGAACCAGCCCGCGAGACATAGTGAGACCCTGTC A G SNRPD3,GGT1 Ensembl:ENSG00000100028,Ensembl:ENSG00000286070 Protein coding,Protein coding 3'UTR,intron GSE38233;GSE100210;GSE99789;GSE107867;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;ASD brains,cerebellum;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,29796672,30559470,30559470,31158229,32596459 RNA-Seq:(High) rs990199072 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1028644,Human_RBP_ID_14420397,Human_RBP_ID_17983213,Human_RBP_ID_18785907,Human_RBP_ID_23011518,Human_RBP_ID_26500849 32940 RMVar_ID_32940 Human_SNP_ID_700142659 A-to-I Human chr22 + 24573019 24573019 24573019 TTTGAGAGGAGTTCAAAACCAGCCCGCGAGACATAGTGAGACCCTGTCTCTACAAAAAATTCTAA TTTGAGAGGAGTTCAAAACCAGCCCGCGAGACGTAGTGAGACCCTGTCTCTACAAAAAATTCTAA A G SNRPD3,GGT1 Ensembl:ENSG00000100028,Ensembl:ENSG00000286070 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1295699990 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26497159 32941 RMVar_ID_32941 Human_SNP_ID_700142660 A-to-I Human chr22 + 24573021 24573021 24573021 TGAGAGGAGTTCAAAACCAGCCCGCGAGACATAGTGAGACCCTGTCTCTACAAAAAATTCTAAAA TGAGAGGAGTTCAAAACCAGCCCGCGAGACATGGTGAGACCCTGTCTCTACAAAAAATTCTAAAA A G SNRPD3,GGT1 Ensembl:ENSG00000100028,Ensembl:ENSG00000286070 Protein coding,Protein coding 3'UTR,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1141314 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26497159 32942 RMVar_ID_32942 Human_SNP_ID_700142665 A-to-I Human chr22 + 24573042 24573042 24573042 CCGCGAGACATAGTGAGACCCTGTCTCTACAAAAAATTCTAAAAATTAACTTGGCATGGTGGTGC CCGCGAGACATAGTGAGACCCTGTCTCTACAACAAATTCTAAAAATTAACTTGGCATGGTGGTGC A C SNRPD3,GGT1 Ensembl:ENSG00000100028,Ensembl:ENSG00000286070 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs776481424 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17983214 32943 RMVar_ID_32943 Human_SNP_ID_700142677 A-to-I Human chr22 + 24573096 24573096 24573096 CATGGTGGTGCACACCTGTAGTCCTCGCTACTAGGGAGGCTGAGGTGGGAGGATCACTTGAGCCT CATGGTGGTGCACACCTGTAGTCCTCGCTACTGGGGAGGCTGAGGTGGGAGGATCACTTGAGCCT A G SNRPD3,GGT1 Ensembl:ENSG00000100028,Ensembl:ENSG00000286070 Protein coding,Protein coding 3'UTR,intron GSE38233;GSE100210;GSE107867;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;ASD brains,cerebellum;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,30559470,32596459 RNA-Seq:(High) rs909009328 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8546989,Human_RBP_ID_26500067 32944 RMVar_ID_32944 Human_SNP_ID_700142696 A-to-I Human chr22 + 24573191 24573190 24573191 TTGCCACTGTACTCCAGCCTGGGCAAAAGAGCAAGACTTTGTCTTTAAAGAAAAATAAGTAGTAG TTGCCACTGTACTCCAGCCTGGGCAAAAGAGC_AGACTTTGTCTTTAAAGAAAAATAAGTAGTAG CA C SNRPD3,GGT1 Ensembl:ENSG00000100028,Ensembl:ENSG00000286070 Protein coding,Protein coding 3'UTR,intron GSE38233;GSE100210;GSE107867;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,30559470,32596459 RNA-Seq:(High) rs777908258 Functional Loss DEL dbSNP153 33..33 33 - - - 32945 RMVar_ID_32945 Human_SNP_ID_700142778 A-to-I Human chr22 + 24573625 24573625 24573625 GGCCAAACATGGTGCCCCACGCCTATAATGCCAGCACTTTGGGAGGTCGAGGCGGGAGGATCACT GGCCAAACATGGTGCCCCACGCCTATAATGCCCGCACTTTGGGAGGTCGAGGCGGGAGGATCACT A C SNRPD3,GGT1 Ensembl:ENSG00000100028,Ensembl:ENSG00000286070 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs368627433 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7067031,Human_RBP_ID_23938437,Human_RBP_ID_26497169 32946 RMVar_ID_32946 Human_SNP_ID_700142814 A-to-I Human chr22 + 24573760 24573760 24573760 TTGAAAAGTAGCTGGGCACAGCTGATGCCTGCAGTCCCAGCTATCCTGGAGGTTGAGGCAGGACG TTGAAAAGTAGCTGGGCACAGCTGATGCCTGCGGTCCCAGCTATCCTGGAGGTTGAGGCAGGACG A G SNRPD3,GGT1 Ensembl:ENSG00000100028,Ensembl:ENSG00000286070 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs951071378 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4689379,Human_RBP_ID_8207874,Human_RBP_ID_14420424,Human_RBP_ID_17399986,Human_RBP_ID_26500072 32947 RMVar_ID_32947 Human_SNP_ID_700143001 A-to-I Human chr22 + 24574596 24574596 24574596 AGACGGTCTCACTCTTCCCCAGGCGGGAGTGCAATGGCACAATCATGGCTCACTGCAGCCTCAAC AGACGGTCTCACTCTTCCCCAGGCGGGAGTGCTATGGCACAATCATGGCTCACTGCAGCCTCAAC A T SNRPD3,GGT1 Ensembl:ENSG00000100028,Ensembl:ENSG00000286070 Protein coding,Protein coding 3'UTR,intron GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,29796672,31158229,31158229,31158229,32596459,32596459 RNA-Seq:(High) rs1255593609 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26497191 32948 RMVar_ID_32948 Human_SNP_ID_700143004 A-to-I Human chr22 + 24574602 24574602 24574602 TCTCACTCTTCCCCAGGCGGGAGTGCAATGGCACAATCATGGCTCACTGCAGCCTCAACCTTCTC TCTCACTCTTCCCCAGGCGGGAGTGCAATGGCTCAATCATGGCTCACTGCAGCCTCAACCTTCTC A T SNRPD3,GGT1 Ensembl:ENSG00000100028,Ensembl:ENSG00000286070 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1255963486 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26497191 32949 RMVar_ID_32949 Human_SNP_ID_700143016 A-to-I Human chr22 + 24574641 24574641 24574641 TGGCTCACTGCAGCCTCAACCTTCTCGGGCTCAGGTGATTCTCCCACCTCAGCCTCCTGAGTAGC TGGCTCACTGCAGCCTCAACCTTCTCGGGCTCGGGTGATTCTCCCACCTCAGCCTCCTGAGTAGC A G SNRPD3,GGT1 Ensembl:ENSG00000100028,Ensembl:ENSG00000286070 Protein coding,Protein coding 3'UTR,intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs910842642 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26497192 32950 RMVar_ID_32950 Human_SNP_ID_700143018 A-to-I Human chr22 + 24574654 24574654 24574654 CCTCAACCTTCTCGGGCTCAGGTGATTCTCCCACCTCAGCCTCCTGAGTAGCTAGAAATACTGGT CCTCAACCTTCTCGGGCTCAGGTGATTCTCCCGCCTCAGCCTCCTGAGTAGCTAGAAATACTGGT A G SNRPD3,GGT1 Ensembl:ENSG00000100028,Ensembl:ENSG00000286070 Protein coding,Protein coding 3'UTR,intron GSE100210;GSE107867;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;ASD brains,cerebellum;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,30559470,32596459 RNA-Seq:(High) rs1386912712 Functional Loss SNV dbSNP153 33..33 33 - - - 32951 RMVar_ID_32951 Human_SNP_ID_700143023 A-to-I Human chr22 + 24574691 24574691 24574691 AGCCTCCTGAGTAGCTAGAAATACTGGTGCACACCACCATGCCTAGCTAATTTTTGTATTTTTTG AGCCTCCTGAGTAGCTAGAAATACTGGTGCACGCCACCATGCCTAGCTAATTTTTGTATTTTTTG A G SNRPD3,GGT1 Ensembl:ENSG00000100028,Ensembl:ENSG00000286070 Protein coding,Protein coding 3'UTR,intron GSE107867 ASD brains,cerebellum;ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs957957412 Functional Loss SNV dbSNP153 33..33 33 - - - 32952 RMVar_ID_32952 Human_SNP_ID_700143027 A-to-I Human chr22 + 24574703 24574703 24574703 AGCTAGAAATACTGGTGCACACCACCATGCCTAGCTAATTTTTGTATTTTTTGTAGAGACAGGGT AGCTAGAAATACTGGTGCACACCACCATGCCTGGCTAATTTTTGTATTTTTTGTAGAGACAGGGT A G SNRPD3,GGT1 Ensembl:ENSG00000100028,Ensembl:ENSG00000286070 Protein coding,Protein coding 3'UTR,intron GSE99789;GSE107867;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,EC109;ASD brains,temporal_cortex;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29796672,30559470,31158229,32596459 RNA-Seq:(High) rs1569029572 Functional Loss SNV dbSNP153 33..33 33 - - - 32953 RMVar_ID_32953 Human_SNP_ID_700143034 A-to-I Human chr22 + 24574742 24574742 24574742 TTTTGTATTTTTTGTAGAGACAGGGTTTTGCCATGTTGCCCAAGCTGGTCTTGAACTCCGGGGCT TTTTGTATTTTTTGTAGAGACAGGGTTTTGCCGTGTTGCCCAAGCTGGTCTTGAACTCCGGGGCT A G SNRPD3,GGT1 Ensembl:ENSG00000100028,Ensembl:ENSG00000286070 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1141318 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4710726,Human_RBP_ID_26497193 32954 RMVar_ID_32954 Human_SNP_ID_700143051 A-to-I Human chr22 + 24574776 24574776 24574776 GTTGCCCAAGCTGGTCTTGAACTCCGGGGCTCAAGTGATCTGCCCGCCTCGGCCTGCTGGGATTA GTTGCCCAAGCTGGTCTTGAACTCCGGGGCTCGAGTGATCTGCCCGCCTCGGCCTGCTGGGATTA A G SNRPD3,GGT1 Ensembl:ENSG00000100028,Ensembl:ENSG00000286070 Protein coding,Protein coding 3'UTR,intron GSE38233;GSE100210;GSE100210;GSE107867 cultured B-cells;HepG2 cell line;HepG2 cell line;ASD brains,temporal_cortex - 24183664,29129909,29129909,30559470 RNA-Seq:(High) rs1198336441 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7067049,Human_RBP_ID_23186404 32955 RMVar_ID_32955 Human_SNP_ID_700143195 A-to-I Human chr22 + 24575370 24575370 24575370 AATTAGTGCCGGGCGCAGTGGCTCATTCCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGTGG AATTAGTGCCGGGCGCAGTGGCTCATTCCTGTCATCCCAGCACTTTGGGAGGCCGAGGTGGGTGG A C SNRPD3,GGT1 Ensembl:ENSG00000100028,Ensembl:ENSG00000286070 Protein coding,Protein coding intron,intron GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-Seq:(High) rs1485938209 Functional Loss SNV dbSNP153 33..33 33 - - - 32956 RMVar_ID_32956 Human_SNP_ID_700143417 A-to-I Human chr22 + 24576032 24576032 24576032 AAAGTGCTGGGATTACAGGCGTGAGCCACCGCACCCGGCCAGAGTCCAGATCCTTTTTATATGAC AAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCCCGGCCAGAGTCCAGATCCTTTTTATATGAC A G SNRPD3,GGT1 Ensembl:ENSG00000100028,Ensembl:ENSG00000286070 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1282277594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7067063,Human_RBP_ID_23186415 32957 RMVar_ID_32957 Human_SNP_ID_700143418 A-to-I Human chr22 + 24576032 24576032 24576032 AAAGTGCTGGGATTACAGGCGTGAGCCACCGCACCCGGCCAGAGTCCAGATCCTTTTTATATGAC AAAGTGCTGGGATTACAGGCGTGAGCCACCGCTCCCGGCCAGAGTCCAGATCCTTTTTATATGAC A T SNRPD3,GGT1 Ensembl:ENSG00000100028,Ensembl:ENSG00000286070 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1282277594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7067063,Human_RBP_ID_23186415 32958 RMVar_ID_32958 Human_SNP_ID_700143486 A-to-I Human chr22 + 24576267 24576267 24576267 TGTCTGTGGTTTTTCTTTTTCTTTTTTTTTTTAAAGACTGAGTTTCACGCTTGTTGCCCAGGCTG TGTCTGTGGTTTTTCTTTTTCTTTTTTTTTTTGAAGACTGAGTTTCACGCTTGTTGCCCAGGCTG A G SNRPD3,GGT1 Ensembl:ENSG00000100028,Ensembl:ENSG00000286070 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1158646814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_576841,Human_RBP_ID_2713683,Human_RBP_ID_7067069,Human_RBP_ID_14420487 32959 RMVar_ID_32959 Human_SNP_ID_700143487 A-to-I Human chr22 + 24576267 24576267 24576267 TGTCTGTGGTTTTTCTTTTTCTTTTTTTTTTTAAAGACTGAGTTTCACGCTTGTTGCCCAGGCTG TGTCTGTGGTTTTTCTTTTTCTTTTTTTTTTTTAAGACTGAGTTTCACGCTTGTTGCCCAGGCTG A T SNRPD3,GGT1 Ensembl:ENSG00000100028,Ensembl:ENSG00000286070 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1158646814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_576841,Human_RBP_ID_2713683,Human_RBP_ID_7067069,Human_RBP_ID_14420487 32960 RMVar_ID_32960 Human_SNP_ID_700143503 A-to-I Human chr22 + 24576325 24576325 24576325 CAGGCTGGAGTGAAATGGTGCCATCTCGGCTCACTGCAACCTTTGCCTCCGGTGTTCAAGCAATT CAGGCTGGAGTGAAATGGTGCCATCTCGGCTCGCTGCAACCTTTGCCTCCGGTGTTCAAGCAATT A G SNRPD3,GGT1 Ensembl:ENSG00000100028,Ensembl:ENSG00000286070 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1011540809 Functional Loss SNV dbSNP153 33..33 33 - - - 32961 RMVar_ID_32961 Human_SNP_ID_700143530 A-to-I Human chr22 + 24576435 24576435 24576435 CCAACACCCGGCTAATTTTTTGTATTTTTAGTAGAGGCAGATTTTCACCATGTTGGTCAGGCTGG CCAACACCCGGCTAATTTTTTGTATTTTTAGTGGAGGCAGATTTTCACCATGTTGGTCAGGCTGG A G SNRPD3,GGT1 Ensembl:ENSG00000100028,Ensembl:ENSG00000286070 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1298379947 Functional Loss SNV dbSNP153 33..33 33 - - - 32962 RMVar_ID_32962 Human_SNP_ID_700143532 A-to-I Human chr22 + 24576452 24576452 24576452 TTTTGTATTTTTAGTAGAGGCAGATTTTCACCATGTTGGTCAGGCTGGTCTCAAACTCGTGACCT TTTTGTATTTTTAGTAGAGGCAGATTTTCACCGTGTTGGTCAGGCTGGTCTCAAACTCGTGACCT A G SNRPD3,GGT1 Ensembl:ENSG00000100028,Ensembl:ENSG00000286070 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1215609569 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7067071 32963 RMVar_ID_32963 Human_SNP_ID_700143538 A-to-I Human chr22 + 24576472 24576472 24576472 CAGATTTTCACCATGTTGGTCAGGCTGGTCTCAAACTCGTGACCTCGGGTGATCCACCTGCCTTG CAGATTTTCACCATGTTGGTCAGGCTGGTCTCGAACTCGTGACCTCGGGTGATCCACCTGCCTTG A G SNRPD3,GGT1 Ensembl:ENSG00000100028,Ensembl:ENSG00000286070 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs921712842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7067071,Human_RBP_ID_14420490 32964 RMVar_ID_32964 Human_SNP_ID_700143552 A-to-I Human chr22 + 24576512 24576512 24576512 GACCTCGGGTGATCCACCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCAGG GACCTCGGGTGATCCACCTGCCTTGGCCTCCCGAAGTGCTGGGATTACAGGCGTGAGCCACCAGG A G SNRPD3,GGT1 Ensembl:ENSG00000100028,Ensembl:ENSG00000286070 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs936809430 Functional Loss SNV dbSNP153 33..33 33 - - - 32965 RMVar_ID_32965 Human_SNP_ID_700143559 A-to-I Human chr22 + 24576542 24576542 24576542 CCAAAGTGCTGGGATTACAGGCGTGAGCCACCAGGCCCGGCTGTCTGTGGTTTTTCTTTCTGGAA CCAAAGTGCTGGGATTACAGGCGTGAGCCACCGGGCCCGGCTGTCTGTGGTTTTTCTTTCTGGAA A G SNRPD3,GGT1 Ensembl:ENSG00000100028,Ensembl:ENSG00000286070 Protein coding,Protein coding intron,intron GSE38233;GSE100210;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 24183664,29129909,30559470 RNA-Seq:(High) rs1323497544 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_576842 32966 RMVar_ID_32966 Human_SNP_ID_700145071 A-to-I Human chr22 + 24582925 24582925 24582925 TTTTTTTTTTTTAGTAGAGATGGGGTTTTGCCATGTTGGCCAGCCTGGTCTTGAACTTCTGACCT TTTTTTTTTTTTAGTAGAGATGGGGTTTTGCCTTGTTGGCCAGCCTGGTCTTGAACTTCTGACCT A T GGT1 Ensembl:ENSG00000286070 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs570136841 Functional Loss SNV dbSNP153 33..33 33 - - - 32967 RMVar_ID_32967 Human_SNP_ID_700145073 A-to-I Human chr22 + 24582934 24582934 24582934 TTTAGTAGAGATGGGGTTTTGCCATGTTGGCCAGCCTGGTCTTGAACTTCTGACCTCCACCCGCC TTTAGTAGAGATGGGGTTTTGCCATGTTGGCCGGCCTGGTCTTGAACTTCTGACCTCCACCCGCC A G GGT1 Ensembl:ENSG00000286070 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1158756959 Functional Loss SNV dbSNP153 33..33 33 - - - 32968 RMVar_ID_32968 Human_SNP_ID_700164390 A-to-I Human chr22 - 24648742 24648742 24648742 AGGGTGATGCAGAGGCCACAGGTGCTGCACGCACCAGCACCCGCTCTAGACATCAGCCTCCAGGT AGGGTGATGCAGAGGCCACAGGTGCTGCACGCTCCAGCACCCGCTCTAGACATCAGCCTCCAGGT T A AP000356.2 Ensembl:ENSG00000284070 lincRNA exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs879126994 Functional Loss SNV dbSNP153 33..33 33 - - - 32969 RMVar_ID_32969 Human_SNP_ID_700164391 A-to-I Human chr22 - 24648742 24648742 24648742 AGGGTGATGCAGAGGCCACAGGTGCTGCACGCACCAGCACCCGCTCTAGACATCAGCCTCCAGGT AGGGTGATGCAGAGGCCACAGGTGCTGCACGCGCCAGCACCCGCTCTAGACATCAGCCTCCAGGT T C AP000356.2 Ensembl:ENSG00000284070 lincRNA exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs879126994 Functional Loss SNV dbSNP153 33..33 33 - - - 32970 RMVar_ID_32970 Human_SNP_ID_700164392 A-to-I Human chr22 - 24648742 24648742 24648742 AGGGTGATGCAGAGGCCACAGGTGCTGCACGCACCAGCACCCGCTCTAGACATCAGCCTCCAGGT AGGGTGATGCAGAGGCCACAGGTGCTGCACGCCCCAGCACCCGCTCTAGACATCAGCCTCCAGGT T G AP000356.2 Ensembl:ENSG00000284070 lincRNA exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs879126994 Functional Loss SNV dbSNP153 33..33 33 - - - 32971 RMVar_ID_32971 Human_SNP_ID_700181660 A-to-I Human chr22 - 24712426 24712426 24712426 TAGCAGGGGTGGTTGCCGTAGGGTTTGCCTTCATGCTCAGCGTGGCCCCCGGAAGTCAGCGTCTT TAGCAGGGGTGGTTGCCGTAGGGTTTGCCTTCGTGCTCAGCGTGGCCCCCGGAAGTCAGCGTCTT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879066871 Functional Loss SNV dbSNP153 33..33 33 - - - 32972 RMVar_ID_32972 Human_SNP_ID_700249567 A-to-I Human chr22 + 24964637 24964637 24964637 TAGAGACAGGATCTTGGTATGTTGCCCTGGCTAGTCTTGAACTCCTAGTCTCAAGTGATTCTTCC TAGAGACAGGATCTTGGTATGTTGCCCTGGCTGGTCTTGAACTCCTAGTCTCAAGTGATTCTTCC A G KIAA1671 Ensembl:ENSG00000197077 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1272125311 Functional Loss SNV dbSNP153 33..33 33 - - - 32973 RMVar_ID_32973 Human_SNP_ID_700266352 A-to-I Human chr22 + 25030441 25030441 25030441 CCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACTCGGGAGGCAGAGGTT CCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCCGGAGAATCGCTTGAACTCGGGAGGCAGAGGTT A C KIAA1671 Ensembl:ENSG00000197077 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1288660713 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_308931,RMVar_hsa_circ_327885,RMVar_hsa_circ_369099 32974 RMVar_ID_32974 Human_SNP_ID_700291075 A-to-I Human chr22 + 25129761 25129761 25129761 CTCACTTACTTCAGGCTAGAACTCCTGGGTTCAAGGACTCTTCCTGCCTCAGCCTCCCAAGTAGC CTCACTTACTTCAGGCTAGAACTCCTGGGTTCGAGGACTCTTCCTGCCTCAGCCTCCCAAGTAGC A G KIAA1671 Ensembl:ENSG00000197077 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs915711628 Functional Loss SNV dbSNP153 33..33 33 - - - 32975 RMVar_ID_32975 Human_SNP_ID_700303296 A-to-I Human chr22 + 25180041 25180041 25180041 AAAGGGACAGAGATGTGGAAAGAACATTCTGAAAGAGGCAAGACCTGGTGCTCTGGAGCCCTTGG AAAGGGACAGAGATGTGGAAAGAACATTCTGAGAGAGGCAAGACCTGGTGCTCTGGAGCCCTTGG A G KIAA1671 Ensembl:ENSG00000197077 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1336956899 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269434 32976 RMVar_ID_32976 Human_SNP_ID_700352129 A-to-I Human chr22 - 25354219 25354219 25354219 CAGAGCTGCACAACTCACAGGTGCCGAGCTCAAGACTCACTCCTGGGTCTGCCTGGGCTGGGCTG CAGAGCTGCACAACTCACAGGTGCCGAGCTCAGGACTCACTCCTGGGTCTGCCTGGGCTGGGCTG T C LRP5L Ensembl:ENSG00000100068 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388844662 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86546,RMVar_hsa_circ_120615,RMVar_hsa_circ_117364,RMVar_hsa_circ_213387,RMVar_hsa_circ_213388,RMVar_hsa_circ_213389,RMVar_hsa_circ_213390 32977 RMVar_ID_32977 Human_SNP_ID_700364856 A-to-I Human chr22 - 25397583 25397583 25397583 ATTGATGCCGGGCACAGTGGCTCACCCCAGTAATCCCAGCACTTTGGGAGGTTGAGGCAGGAGGA ATTGATGCCGGGCACAGTGGCTCACCCCAGTATTCCCAGCACTTTGGGAGGTTGAGGCAGGAGGA T A LRP5L Ensembl:ENSG00000100068 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs537157602 Functional Loss SNV dbSNP153 33..33 33 - - - 32978 RMVar_ID_32978 Human_SNP_ID_700364857 A-to-I Human chr22 - 25397583 25397583 25397583 ATTGATGCCGGGCACAGTGGCTCACCCCAGTAATCCCAGCACTTTGGGAGGTTGAGGCAGGAGGA ATTGATGCCGGGCACAGTGGCTCACCCCAGTAGTCCCAGCACTTTGGGAGGTTGAGGCAGGAGGA T C LRP5L Ensembl:ENSG00000100068 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs537157602 Functional Loss SNV dbSNP153 33..33 33 - - - 32979 RMVar_ID_32979 Human_SNP_ID_700364858 A-to-I Human chr22 - 25397584 25397584 25397584 TATTGATGCCGGGCACAGTGGCTCACCCCAGTAATCCCAGCACTTTGGGAGGTTGAGGCAGGAGG TATTGATGCCGGGCACAGTGGCTCACCCCAGTGATCCCAGCACTTTGGGAGGTTGAGGCAGGAGG T C LRP5L Ensembl:ENSG00000100068 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1191943834 Functional Loss SNV dbSNP153 33..33 33 - - - 32980 RMVar_ID_32980 Human_SNP_ID_700364962 A-to-I Human chr22 - 25398024 25398024 25398024 CCAGTCTGGTCTTGAACTCCTGGCATCCAGCTATCCTCCCACGTCAGCCTTCCAAAGTGTTGGGA CCAGTCTGGTCTTGAACTCCTGGCATCCAGCTGTCCTCCCACGTCAGCCTTCCAAAGTGTTGGGA T C LRP5L Ensembl:ENSG00000100068 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs747743288 Functional Loss SNV dbSNP153 33..33 33 - - - 32981 RMVar_ID_32981 Human_SNP_ID_700365425 A-to-I Human chr22 - 25399715 25399715 25399715 TTGCCCAGGCTAGAGTGCAGTGGTGCGATCTCAGCTCACTGCAAGCTCCACCTCCTGAGTTCACA TTGCCCAGGCTAGAGTGCAGTGGTGCGATCTCTGCTCACTGCAAGCTCCACCTCCTGAGTTCACA T A LRP5L Ensembl:ENSG00000100068 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs905831137 Functional Loss SNV dbSNP153 33..33 33 - - - 32982 RMVar_ID_32982 Human_SNP_ID_700384054 A-to-I Human chr22 + 25466973 25466966 25466973 GATCAGGAGCCTTGGTTCAGGCCTATAATCCCAACACTTTGGGAAACTGAGGTGGGAGGATCGCT GATCAGGAGCCTTGGTTCAGGCCTAT_______ACACTTTGGGAAACTGAGGTGGGAGGATCGCT TAATCCCA T CRYBB2P1 Ensembl:ENSG00000100058 Pseudogene intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs552730153 Functional Loss DEL dbSNP153 27..33 33 - - - Human_RBP_ID_18535544,Human_RBP_ID_22267818 32983 RMVar_ID_32983 Human_SNP_ID_700427869 A-to-I Human chr22 + 25649039 25649039 25649039 GGGCAGAGTGCCATATCCAGGTATGGTGAACCATGAAATACTGGAACAGGTGGAGCGAGGATACA GGGCAGAGTGCCATATCCAGGTATGGTGAACCGTGAAATACTGGAACAGGTGGAGCGAGGATACA A G YES1P1,GRK3 Ensembl:ENSG00000224003,Ensembl:ENSG00000100077 Pseudogene,Protein coding exon,intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs543833665 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1213,RMVar_hsa_circ_288124,RMVar_hsa_circ_311471,RMVar_hsa_circ_326983,RMVar_hsa_circ_318715,RMVar_hsa_circ_274145,RMVar_hsa_circ_213408,RMVar_hsa_circ_213410,RMVar_hsa_circ_213411,RMVar_hsa_circ_213409,RMVar_hsa_circ_293944,RMVar_hsa_circ_322436,RMVar_hsa_circ_330158,RMVar_hsa_circ_326069,RMVar_hsa_circ_299274,RMVar_hsa_circ_64654,RMVar_hsa_circ_213415,RMVar_hsa_circ_213417,RMVar_hsa_circ_213418,RMVar_hsa_circ_213416 32984 RMVar_ID_32984 Human_SNP_ID_700445537 A-to-I Human chr22 + 25724900 25724900 25724900 TTTAATTTTTTGGGATAGGGCCTCGCTCTGTCACCCAGGCTGGAGAACAGTGGGATGATCATGGC TTTAATTTTTTGGGATAGGGCCTCGCTCTGTCGCCCAGGCTGGAGAACAGTGGGATGATCATGGC A G GRK3 Ensembl:ENSG00000100077 Protein coding 3'UTR GSE38233;GSE107867 cultured B-cells;ASD brains,frontal_cortex - 24183664,30559470 RNA-Seq:(High) rs1025450936 Functional Loss SNV dbSNP153 33..33 33 - - - 32985 RMVar_ID_32985 Human_SNP_ID_700445550 A-to-I Human chr22 + 25724978 25724978 25724978 GAATTCCTAGGTTCAAGCAATCCTCCCACGTCAGCCTCCTGAGTAGCTAGGACTACAGGTGCATG GAATTCCTAGGTTCAAGCAATCCTCCCACGTCTGCCTCCTGAGTAGCTAGGACTACAGGTGCATG A T GRK3 Ensembl:ENSG00000100077 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs989988025 Functional Loss SNV dbSNP153 33..33 33 - - - 32986 RMVar_ID_32986 Human_SNP_ID_700445556 A-to-I Human chr22 + 25725000 25725000 25725000 CTCCCACGTCAGCCTCCTGAGTAGCTAGGACTACAGGTGCATGCCACCTTTCCTGGCTAATTTAT CTCCCACGTCAGCCTCCTGAGTAGCTAGGACTGCAGGTGCATGCCACCTTTCCTGGCTAATTTAT A G GRK3 Ensembl:ENSG00000100077 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs145534957 Functional Loss SNV dbSNP153 33..33 33 - - - 32987 RMVar_ID_32987 Human_SNP_ID_700445724 A-to-I Human chr22 + 25725828 25725828 25725828 AAAATTAGCCGGGCGTGGTGGCGGGCGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA AAAATTAGCCGGGCGTGGTGGCGGGCGCCTGTGGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA A G GRK3 Ensembl:ENSG00000100077 Protein coding 3'UTR GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line - 24183664,31158229 RNA-Seq:(High) rs1480812410 Functional Loss SNV dbSNP153 33..33 33 - - - 32988 RMVar_ID_32988 Human_SNP_ID_700445725 A-to-I Human chr22 + 25725834 25725834 25725834 AGCCGGGCGTGGTGGCGGGCGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATGGCA AGCCGGGCGTGGTGGCGGGCGCCTGTAGTCCCGGCTACTTGGGAGGCTGAGGCAGGAGAATGGCA A G GRK3 Ensembl:ENSG00000100077 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1190425948 Functional Loss SNV dbSNP153 33..33 33 - - - 32989 RMVar_ID_32989 Human_SNP_ID_700445731 A-to-I Human chr22 + 25725855 25725855 25725855 CCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATGGCATGAACCCGGGAGGCAGAGCTT CCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCGGGAGAATGGCATGAACCCGGGAGGCAGAGCTT A G GRK3 Ensembl:ENSG00000100077 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1422260684 Functional Loss SNV dbSNP153 33..33 33 - - - 32990 RMVar_ID_32990 Human_SNP_ID_700445734 A-to-I Human chr22 + 25725869 25725869 25725869 TACTTGGGAGGCTGAGGCAGGAGAATGGCATGAACCCGGGAGGCAGAGCTTGCAGTGAGCCGAGA TACTTGGGAGGCTGAGGCAGGAGAATGGCATGGACCCGGGAGGCAGAGCTTGCAGTGAGCCGAGA A G GRK3 Ensembl:ENSG00000100077 Protein coding 3'UTR GSE47997;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,31158229,31158229,31158229,31158229 RNA-Seq:(High) rs1356816696 Functional Loss SNV dbSNP153 33..33 33 - - - 32991 RMVar_ID_32991 Human_SNP_ID_700564568 A-to-I Human chr22 + 26202175 26202175 26202175 TGATCTCGTGATCCACCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACTGCGC TGATCTCGTGATCCACCTGCCTCGGCCTCCCAGAGTGCTGGGATTACAGGTGTGAGCCACTGCGC A G SEZ6L Ensembl:ENSG00000100095 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1429981825 Functional Loss SNV dbSNP153 33..33 33 - - - 32992 RMVar_ID_32992 Human_SNP_ID_700635638 A-to-I Human chr22 - 26475418 26475418 26475418 AACCTGGGAGGCAGAGGTTACAGTGAGCTGAGATCGCGCCATTGCACTCCAGCCTGGGCAACAAA AACCTGGGAGGCAGAGGTTACAGTGAGCTGAGGTCGCGCCATTGCACTCCAGCCTGGGCAACAAA T C HPS4 Ensembl:ENSG00000100099 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs980543125 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9028,RMVar_hsa_circ_33388,RMVar_hsa_circ_348879,RMVar_hsa_circ_62380,RMVar_hsa_circ_213473,RMVar_hsa_circ_213475 32993 RMVar_ID_32993 Human_SNP_ID_700635665 A-to-I Human chr22 - 26475555 26475555 26475555 CTGAGGTCAGGAATTCAAGACCAGCCTGACCAACATGGAGAAACCCTGTCTGTACTAAAAATACA CTGAGGTCAGGAATTCAAGACCAGCCTGACCAGCATGGAGAAACCCTGTCTGTACTAAAAATACA T C HPS4 Ensembl:ENSG00000100099 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs959158074 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9028,RMVar_hsa_circ_33388,RMVar_hsa_circ_348879,RMVar_hsa_circ_62380,RMVar_hsa_circ_213473,RMVar_hsa_circ_213475 32994 RMVar_ID_32994 Human_SNP_ID_700635739 A-to-I Human chr22 - 26475927 26475927 26475927 ACGATCCTCCCATCTCAGCCTCCTGAGTTGCTAGGACCACAGGCATGCACCACCATGCCCGGCTA ACGATCCTCCCATCTCAGCCTCCTGAGTTGCTGGGACCACAGGCATGCACCACCATGCCCGGCTA T C HPS4 Ensembl:ENSG00000100099 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs776220689 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9028,RMVar_hsa_circ_33388,RMVar_hsa_circ_348879,RMVar_hsa_circ_62380,RMVar_hsa_circ_213473,RMVar_hsa_circ_213475 32995 RMVar_ID_32995 Human_SNP_ID_700635759 A-to-I Human chr22 - 26475980 26475980 26475980 GGAGTGCTGAGGTGTGACCTTGGTTTACTGCAACCTCCGCCTCCCAGGCTCAAACGATCCTCCCA GGAGTGCTGAGGTGTGACCTTGGTTTACTGCATCCTCCGCCTCCCAGGCTCAAACGATCCTCCCA T A HPS4 Ensembl:ENSG00000100099 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1371068725 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9028,RMVar_hsa_circ_33388,RMVar_hsa_circ_348879,RMVar_hsa_circ_62380,RMVar_hsa_circ_213473,RMVar_hsa_circ_213475 32996 RMVar_ID_32996 Human_SNP_ID_700635760 A-to-I Human chr22 - 26475980 26475980 26475980 GGAGTGCTGAGGTGTGACCTTGGTTTACTGCAACCTCCGCCTCCCAGGCTCAAACGATCCTCCCA GGAGTGCTGAGGTGTGACCTTGGTTTACTGCAGCCTCCGCCTCCCAGGCTCAAACGATCCTCCCA T C HPS4 Ensembl:ENSG00000100099 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1371068725 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9028,RMVar_hsa_circ_33388,RMVar_hsa_circ_348879,RMVar_hsa_circ_62380,RMVar_hsa_circ_213473,RMVar_hsa_circ_213475 32997 RMVar_ID_32997 Human_SNP_ID_700635863 A-to-I Human chr22 - 26476441 26476441 26476441 TGGGGAGGCTGAGGGGAGGATTGCTTGAGCTTAGGAGTTTCAGGCTGCAGTGAGCCATGATTGCC TGGGGAGGCTGAGGGGAGGATTGCTTGAGCTTGGGAGTTTCAGGCTGCAGTGAGCCATGATTGCC T C HPS4 Ensembl:ENSG00000100099 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167341028 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9028,RMVar_hsa_circ_33388,RMVar_hsa_circ_348879,RMVar_hsa_circ_62380,RMVar_hsa_circ_213473,RMVar_hsa_circ_213475 32998 RMVar_ID_32998 Human_SNP_ID_700635873 A-to-I Human chr22 - 26476479 26476479 26476479 AACCGGGTGTGGTGGCTCATGTCTGTGGTCTTAGCTACTGGGGAGGCTGAGGGGAGGATTGCTTG AACCGGGTGTGGTGGCTCATGTCTGTGGTCTTTGCTACTGGGGAGGCTGAGGGGAGGATTGCTTG T A HPS4 Ensembl:ENSG00000100099 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1306989130 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9028,RMVar_hsa_circ_33388,RMVar_hsa_circ_348879,RMVar_hsa_circ_62380,RMVar_hsa_circ_213473,RMVar_hsa_circ_213475 32999 RMVar_ID_32999 Human_SNP_ID_700648588 A-to-I Human chr22 - 26522998 26522998 26522998 ACCTCTAACTCCTGCAAACACAGCTCACTGCAACCTCTAACTCCTGGGCTCAAGCAGTCCTTTCA ACCTCTAACTCCTGCAAACACAGCTCACTGCAGCCTCTAACTCCTGGGCTCAAGCAGTCCTTTCA T C TPST2 Ensembl:ENSG00000128294 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1440275408 Functional Loss SNV dbSNP153 33..33 33 - - - 33000 RMVar_ID_33000 Human_SNP_ID_700648589 A-to-I Human chr22 - 26522998 26522998 26522998 ACCTCTAACTCCTGCAAACACAGCTCACTGCAACCTCTAACTCCTGGGCTCAAGCAGTCCTTTCA ACCTCTAACTCCTGCAAACACAGCTCACTGCACCCTCTAACTCCTGGGCTCAAGCAGTCCTTTCA T G TPST2 Ensembl:ENSG00000128294 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1440275408 Functional Loss SNV dbSNP153 33..33 33 - - - 33001 RMVar_ID_33001 Human_SNP_ID_700650306 A-to-I Human chr22 - 26530341 26530341 26530341 TAGCCATCCAAAATGGTGCTAGTGAAACCCAAATGATGAAAAAATAGTAAGAAAGCAAAACAAAG TAGCCATCCAAAATGGTGCTAGTGAAACCCAAGTGATGAAAAAATAGTAAGAAAGCAAAACAAAG T C TPST2 Ensembl:ENSG00000128294 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1002276672 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_213484,RMVar_hsa_circ_79870,RMVar_hsa_circ_88964,RMVar_hsa_circ_213485,RMVar_hsa_circ_86143,RMVar_hsa_circ_213487,RMVar_hsa_circ_213488 33002 RMVar_ID_33002 Human_SNP_ID_700650549 A-to-I Human chr22 - 26531292 26531292 26531292 TAGTGTTCTGTGGAATGCATGTGCTACCATTTACTAAACAGCTTCTTCAAGACCATTTCCAGTTT TAGTGTTCTGTGGAATGCATGTGCTACCATTTGCTAAACAGCTTCTTCAAGACCATTTCCAGTTT T C TPST2 Ensembl:ENSG00000128294 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs895365968 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_213484,RMVar_hsa_circ_79870,RMVar_hsa_circ_88964,RMVar_hsa_circ_213485,RMVar_hsa_circ_86143,RMVar_hsa_circ_213487,RMVar_hsa_circ_213488 33003 RMVar_ID_33003 Human_SNP_ID_700650560 A-to-I Human chr22 - 26531355 26531355 26531355 GTTTTGCTTTCTTAATATTTTCCTATCTTTTGAGTTTCACCGGCACCATTTTGGATGGCTACGTA GTTTTGCTTTCTTAATATTTTCCTATCTTTTGCGTTTCACCGGCACCATTTTGGATGGCTACGTA T G TPST2 Ensembl:ENSG00000128294 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1168326742 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_213484,RMVar_hsa_circ_79870,RMVar_hsa_circ_88964,RMVar_hsa_circ_213485,RMVar_hsa_circ_86143,RMVar_hsa_circ_213487,RMVar_hsa_circ_213488 33004 RMVar_ID_33004 Human_SNP_ID_700652500 A-to-I Human chr22 - 26539647 26539647 26539647 CTCCCACCTCAGTCTCCCGAGTAGTTGGGACTACAGGCGAGCATCTCCACACCCAGCTCATTTTT CTCCCACCTCAGTCTCCCGAGTAGTTGGGACTGCAGGCGAGCATCTCCACACCCAGCTCATTTTT T C TPST2 Ensembl:ENSG00000128294 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs940292422 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_358958,RMVar_hsa_circ_213490,RMVar_hsa_circ_292536,RMVar_hsa_circ_317479 33005 RMVar_ID_33005 Human_SNP_ID_700689111 A-to-I Human chr22 + 26678723 26678723 26678723 AGCAAAATGTTGTTGAGTCCTACTGTGTGTCAAATACAATGCTGGGTGCCCAGGGCACAGCAGAC AGCAAAATGTTGTTGAGTCCTACTGTGTGTCAGATACAATGCTGGGTGCCCAGGGCACAGCAGAC A G MIATNB Ensembl:ENSG00000244625 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1163378645 Functional Loss SNV dbSNP153 33..33 33 - - - 33006 RMVar_ID_33006 Human_SNP_ID_700689112 A-to-I Human chr22 + 26678723 26678723 26678723 AGCAAAATGTTGTTGAGTCCTACTGTGTGTCAAATACAATGCTGGGTGCCCAGGGCACAGCAGAC AGCAAAATGTTGTTGAGTCCTACTGTGTGTCATATACAATGCTGGGTGCCCAGGGCACAGCAGAC A T MIATNB Ensembl:ENSG00000244625 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1163378645 Functional Loss SNV dbSNP153 33..33 33 - - - 33007 RMVar_ID_33007 Human_SNP_ID_700697528 A-to-I Human chr22 + 26712655 26712655 26712655 CACGGCTCATTGCAGCCTTGACTCCTGGGCTCAAGCAATCCTCCCACTTCAGCCTCCCGAGTAGC CACGGCTCATTGCAGCCTTGACTCCTGGGCTCGAGCAATCCTCCCACTTCAGCCTCCCGAGTAGC A G MIATNB Ensembl:ENSG00000244625 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1434475672 Functional Loss SNV dbSNP153 33..33 33 - - - 33008 RMVar_ID_33008 Human_SNP_ID_700697575 A-to-I Human chr22 + 26712843 26712843 26712843 TTTCTGCCTCAGCCTCCCAAAGTGTTGGGATTACAGGTGTAAGCCATTATGACTGGTCCGGGGCA TTTCTGCCTCAGCCTCCCAAAGTGTTGGGATTGCAGGTGTAAGCCATTATGACTGGTCCGGGGCA A G MIATNB Ensembl:ENSG00000244625 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs565428552 Functional Loss SNV dbSNP153 33..33 33 - - - 33009 RMVar_ID_33009 Human_SNP_ID_700697576 A-to-I Human chr22 + 26712843 26712843 26712843 TTTCTGCCTCAGCCTCCCAAAGTGTTGGGATTACAGGTGTAAGCCATTATGACTGGTCCGGGGCA TTTCTGCCTCAGCCTCCCAAAGTGTTGGGATTTCAGGTGTAAGCCATTATGACTGGTCCGGGGCA A T MIATNB Ensembl:ENSG00000244625 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs565428552 Functional Loss SNV dbSNP153 33..33 33 - - - 33010 RMVar_ID_33010 Human_SNP_ID_700699009 A-to-I Human chr22 + 26718222 26718222 26718222 AGCGATCCACCCGCCTTGGCCTCCTAAGTCCTAGGATTATAGGTATGAGCCACTGCGCCTGGCCT AGCGATCCACCCGCCTTGGCCTCCTAAGTCCTGGGATTATAGGTATGAGCCACTGCGCCTGGCCT A G MIATNB Ensembl:ENSG00000244625 lincRNA exon GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs151022451 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2148762,Human_Splice_Rec_2148763,Human_Splice_Rec_2148810,Human_Splice_Rec_2148811,Human_Splice_Rec_2148816,Human_Splice_Rec_2148828,Human_Splice_Rec_2148829 RMVar_hsa_circ_213496,RMVar_hsa_circ_352101,RMVar_hsa_circ_351092 33011 RMVar_ID_33011 Human_SNP_ID_700699010 A-to-I Human chr22 + 26718222 26718222 26718222 AGCGATCCACCCGCCTTGGCCTCCTAAGTCCTAGGATTATAGGTATGAGCCACTGCGCCTGGCCT AGCGATCCACCCGCCTTGGCCTCCTAAGTCCTTGGATTATAGGTATGAGCCACTGCGCCTGGCCT A T MIATNB Ensembl:ENSG00000244625 lincRNA exon GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs151022451 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2148762,Human_Splice_Rec_2148763,Human_Splice_Rec_2148810,Human_Splice_Rec_2148811,Human_Splice_Rec_2148816,Human_Splice_Rec_2148828,Human_Splice_Rec_2148829 RMVar_hsa_circ_213496,RMVar_hsa_circ_352101,RMVar_hsa_circ_351092 33012 RMVar_ID_33012 Human_SNP_ID_700701604 A-to-I Human chr22 + 26727530 26727530 26727530 GGCACCAAGCCATTCATGAGGCTTCCACCCCTATGACATAAACACCTTCCACTAGCTCCACCTCC GGCACCAAGCCATTCATGAGGCTTCCACCCCTGTGACATAAACACCTTCCACTAGCTCCACCTCC A G MIATNB Ensembl:ENSG00000244625 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1187703827 Functional Loss SNV dbSNP153 33..33 33 - - - 33013 RMVar_ID_33013 Human_SNP_ID_700702207 A-to-I Human chr22 + 26730104 26730103 26730105 GGGAGGGACCTGGTGGGAGGTAATTTAATCACAGGGGCATTTACCCTCATGCTGTTCTGGTGATA GGGAGGGACCTGGTGGGAGGTAATTTAATCAC__GGGCATTTACCCTCATGCTGTTCTGGTGATA CAG C MIATNB Ensembl:ENSG00000244625 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005066748 Functional Loss DEL dbSNP153 33..34 33 - - - 33014 RMVar_ID_33014 Human_SNP_ID_700702208 A-to-I Human chr22 + 26730104 26730104 26730104 GGGAGGGACCTGGTGGGAGGTAATTTAATCACAGGGGCATTTACCCTCATGCTGTTCTGGTGATA GGGAGGGACCTGGTGGGAGGTAATTTAATCACGGGGGCATTTACCCTCATGCTGTTCTGGTGATA A G MIATNB Ensembl:ENSG00000244625 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1318117982 Functional Loss SNV dbSNP153 33..33 33 - - - 33015 RMVar_ID_33015 Human_SNP_ID_700734102 A-to-I Human chr22 + 26861211 26861210 26861212 AAACACACTCCTGTGTAACCAGCAATGAGCTCAAGACACTCAACATTTCCAGCCCCACCTCAGTC AAACACACTCCTGTGTAACCAGCAATGAGCTC__GACACTCAACATTTCCAGCCCCACCTCAGTC CAA C LINC01422 Ensembl:ENSG00000223704 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1421704363 Functional Loss DEL dbSNP153 33..34 33 - - - 33016 RMVar_ID_33016 Human_SNP_ID_700734103 A-to-I Human chr22 + 26861211 26861211 26861211 AAACACACTCCTGTGTAACCAGCAATGAGCTCAAGACACTCAACATTTCCAGCCCCACCTCAGTC AAACACACTCCTGTGTAACCAGCAATGAGCTCCAGACACTCAACATTTCCAGCCCCACCTCAGTC A C LINC01422 Ensembl:ENSG00000223704 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1299838668 Functional Loss SNV dbSNP153 33..33 33 - - - 33017 RMVar_ID_33017 Human_SNP_ID_701006507 A-to-I Human chr22 - 27898125 27898125 27898125 GTGATCCTCCTGCCTCAGCCTCTCAAAATGCTAGGATTACAGGCATGAGCCACCATACCCAGCTA GTGATCCTCCTGCCTCAGCCTCTCAAAATGCTGGGATTACAGGCATGAGCCACCATACCCAGCTA T C PITPNB Ensembl:ENSG00000180957 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1196499923 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_213500,RMVar_hsa_circ_110113,RMVar_hsa_circ_377179,RMVar_hsa_circ_213504,RMVar_hsa_circ_326922,RMVar_hsa_circ_69086,RMVar_hsa_circ_213506,RMVar_hsa_circ_213508,RMVar_hsa_circ_278571,RMVar_hsa_circ_213513,RMVar_hsa_circ_87014,RMVar_hsa_circ_213514 33018 RMVar_ID_33018 Human_SNP_ID_701006531 A-to-I Human chr22 - 27898253 27898253 27898253 CTCCCACCTGAGCCTCCTGAATAGTTGGGGCTACAGGCATGTGCCACCATGCCTGGCTAGTTTTA CTCCCACCTGAGCCTCCTGAATAGTTGGGGCTGCAGGCATGTGCCACCATGCCTGGCTAGTTTTA T C PITPNB Ensembl:ENSG00000180957 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs117111188 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_213500,RMVar_hsa_circ_110113,RMVar_hsa_circ_377179,RMVar_hsa_circ_213504,RMVar_hsa_circ_326922,RMVar_hsa_circ_69086,RMVar_hsa_circ_213506,RMVar_hsa_circ_213508,RMVar_hsa_circ_278571,RMVar_hsa_circ_213513,RMVar_hsa_circ_87014,RMVar_hsa_circ_213514 33019 RMVar_ID_33019 Human_SNP_ID_701006535 A-to-I Human chr22 - 27898280 27898280 27898280 ACCTCTATCTCCCAGGTTCAAGTGATCCTCCCACCTGAGCCTCCTGAATAGTTGGGGCTACAGGC ACCTCTATCTCCCAGGTTCAAGTGATCCTCCCCCCTGAGCCTCCTGAATAGTTGGGGCTACAGGC T G PITPNB Ensembl:ENSG00000180957 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1366018612 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_213500,RMVar_hsa_circ_110113,RMVar_hsa_circ_377179,RMVar_hsa_circ_213504,RMVar_hsa_circ_326922,RMVar_hsa_circ_69086,RMVar_hsa_circ_213506,RMVar_hsa_circ_213508,RMVar_hsa_circ_278571,RMVar_hsa_circ_213513,RMVar_hsa_circ_87014,RMVar_hsa_circ_213514 33020 RMVar_ID_33020 Human_SNP_ID_701007370 A-to-I Human chr22 - 27901775 27901775 27901775 GAGTCAAGCGACTCTCCTGCCTCAGCCTCCCAAGTGGCTGGGATTGTAGGCACCCGCCACCATGT GAGTCAAGCGACTCTCCTGCCTCAGCCTCCCAGGTGGCTGGGATTGTAGGCACCCGCCACCATGT T C PITPNB Ensembl:ENSG00000180957 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1233955512 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7069351 RMVar_hsa_circ_213500,RMVar_hsa_circ_110113,RMVar_hsa_circ_377179,RMVar_hsa_circ_213504,RMVar_hsa_circ_326922,RMVar_hsa_circ_69086,RMVar_hsa_circ_213506,RMVar_hsa_circ_213508,RMVar_hsa_circ_278571,RMVar_hsa_circ_213513,RMVar_hsa_circ_87014,RMVar_hsa_circ_213514 33021 RMVar_ID_33021 Human_SNP_ID_701007392 A-to-I Human chr22 - 27901879 27901879 27901879 GTATATATATATTTATTATTATTATTTTTGAGACACAGTCTCACTGTGTCCCCAGGCTGAAGTAC GTATATATATATTTATTATTATTATTTTTGAGGCACAGTCTCACTGTGTCCCCAGGCTGAAGTAC T C PITPNB Ensembl:ENSG00000180957 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1409226751 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14431885,Human_RBP_ID_23940209 RMVar_hsa_circ_213500,RMVar_hsa_circ_110113,RMVar_hsa_circ_377179,RMVar_hsa_circ_213504,RMVar_hsa_circ_326922,RMVar_hsa_circ_69086,RMVar_hsa_circ_213506,RMVar_hsa_circ_213508,RMVar_hsa_circ_278571,RMVar_hsa_circ_213513,RMVar_hsa_circ_87014,RMVar_hsa_circ_213514 33022 RMVar_ID_33022 Human_SNP_ID_701008246 A-to-I Human chr22 - 27905296 27905296 27905296 AAAATACAAAAAATTTAGCGGAATGTGGTGGCAGGCACCTGTAATCCCAGCTACTTGGGAGGCTG AAAATACAAAAAATTTAGCGGAATGTGGTGGCGGGCACCTGTAATCCCAGCTACTTGGGAGGCTG T C PITPNB Ensembl:ENSG00000180957 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1254242809 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_213500,RMVar_hsa_circ_110113,RMVar_hsa_circ_377179,RMVar_hsa_circ_213504,RMVar_hsa_circ_326922,RMVar_hsa_circ_69086,RMVar_hsa_circ_213506,RMVar_hsa_circ_213508,RMVar_hsa_circ_278571,RMVar_hsa_circ_213513,RMVar_hsa_circ_87014,RMVar_hsa_circ_213514 33023 RMVar_ID_33023 Human_SNP_ID_701009170 A-to-I Human chr22 - 27909360 27909360 27909360 CATAAATATTTTAAAACAAAAAATGCTGGCCAAGTGTGGTGGCTCAGGCCTATAATCCCAGAACT CATAAATATTTTAAAACAAAAAATGCTGGCCAGGTGTGGTGGCTCAGGCCTATAATCCCAGAACT T C PITPNB Ensembl:ENSG00000180957 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs372050947 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14432272,Human_RBP_ID_17983707 RMVar_hsa_circ_213500,RMVar_hsa_circ_110113,RMVar_hsa_circ_377179,RMVar_hsa_circ_213504,RMVar_hsa_circ_326922,RMVar_hsa_circ_69086,RMVar_hsa_circ_213506,RMVar_hsa_circ_213508,RMVar_hsa_circ_278571,RMVar_hsa_circ_213513,RMVar_hsa_circ_87014,RMVar_hsa_circ_213514 33024 RMVar_ID_33024 Human_SNP_ID_701009380 A-to-I Human chr22 - 27910091 27910091 27910091 AAAAATTAGCCTGGGTGTGGTGGCGCACGCCTATAGTCCCAGCTACTTGGGAGGCTGAGGCAGCA AAAAATTAGCCTGGGTGTGGTGGCGCACGCCTTTAGTCCCAGCTACTTGGGAGGCTGAGGCAGCA T A PITPNB Ensembl:ENSG00000180957 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs546118285 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25660030 RMVar_hsa_circ_213500,RMVar_hsa_circ_110113,RMVar_hsa_circ_377179,RMVar_hsa_circ_213504,RMVar_hsa_circ_326922,RMVar_hsa_circ_69086,RMVar_hsa_circ_213506,RMVar_hsa_circ_213508,RMVar_hsa_circ_278571,RMVar_hsa_circ_213513,RMVar_hsa_circ_87014,RMVar_hsa_circ_213514 33025 RMVar_ID_33025 Human_SNP_ID_701009381 A-to-I Human chr22 - 27910091 27910091 27910091 AAAAATTAGCCTGGGTGTGGTGGCGCACGCCTATAGTCCCAGCTACTTGGGAGGCTGAGGCAGCA AAAAATTAGCCTGGGTGTGGTGGCGCACGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGCA T C PITPNB Ensembl:ENSG00000180957 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs546118285 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25660030 RMVar_hsa_circ_213500,RMVar_hsa_circ_110113,RMVar_hsa_circ_377179,RMVar_hsa_circ_213504,RMVar_hsa_circ_326922,RMVar_hsa_circ_69086,RMVar_hsa_circ_213506,RMVar_hsa_circ_213508,RMVar_hsa_circ_278571,RMVar_hsa_circ_213513,RMVar_hsa_circ_87014,RMVar_hsa_circ_213514 33026 RMVar_ID_33026 Human_SNP_ID_701014527 A-to-I Human chr22 + 27929469 27929469 27929469 CTCCCACTTCAGCCTCCCGAGTAGCTGGGACTACAGGCATGTACCACCCCACCTGGCTAATTTTA CTCCCACTTCAGCCTCCCGAGTAGCTGGGACTGCAGGCATGTACCACCCCACCTGGCTAATTTTA A G TTC28-AS1 Ensembl:ENSG00000235954 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1311597800 Functional Loss SNV dbSNP153 33..33 33 - - - 33027 RMVar_ID_33027 Human_SNP_ID_701018367 A-to-I Human chr22 + 27945837 27945837 27945837 CAAGCAATCCTCCCATCTAGGTCTCCCAAAGTATTGGGATTACGGGCATGAGCCACCATGCCCAG CAAGCAATCCTCCCATCTAGGTCTCCCAAAGTGTTGGGATTACGGGCATGAGCCACCATGCCCAG A G TTC28-AS1 Ensembl:ENSG00000235954 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs964003641 Functional Loss SNV dbSNP153 33..33 33 - - - 33028 RMVar_ID_33028 Human_SNP_ID_701123215 A-to-I Human chr22 - 28393078 28393078 28393078 AGGAGTTTGAGACCAGCCTGAGCAACACAGCAAGACCTCATCTCTACAAAAAATAAATATAAAAC AGGAGTTTGAGACCAGCCTGAGCAACACAGCACGACCTCATCTCTACAAAAAATAAATATAAAAC T G TTC28 Ensembl:ENSG00000100154 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1425651593 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 33029 RMVar_ID_33029 Human_SNP_ID_701123218 A-to-I Human chr22 - 28393086 28393086 28393086 TTGAGCCCAGGAGTTTGAGACCAGCCTGAGCAACACAGCAAGACCTCATCTCTACAAAAAATAAA TTGAGCCCAGGAGTTTGAGACCAGCCTGAGCAGCACAGCAAGACCTCATCTCTACAAAAAATAAA T C TTC28 Ensembl:ENSG00000100154 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1197292132 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 33030 RMVar_ID_33030 Human_SNP_ID_701123219 A-to-I Human chr22 - 28393087 28393087 28393087 CTTGAGCCCAGGAGTTTGAGACCAGCCTGAGCAACACAGCAAGACCTCATCTCTACAAAAAATAA CTTGAGCCCAGGAGTTTGAGACCAGCCTGAGCTACACAGCAAGACCTCATCTCTACAAAAAATAA T A TTC28 Ensembl:ENSG00000100154 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1475237346 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 33031 RMVar_ID_33031 Human_SNP_ID_701123417 A-to-I Human chr22 - 28393938 28393938 28393938 ACCAAGAAGTTTGAGACCAGTTTGGGAAACATAGTAAGACCTCATCTCAAAAACAAAAACAAAAA ACCAAGAAGTTTGAGACCAGTTTGGGAAACATGGTAAGACCTCATCTCAAAAACAAAAACAAAAA T C TTC28 Ensembl:ENSG00000100154 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1016610935 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 33032 RMVar_ID_33032 Human_SNP_ID_701123418 A-to-I Human chr22 - 28393938 28393938 28393938 ACCAAGAAGTTTGAGACCAGTTTGGGAAACATAGTAAGACCTCATCTCAAAAACAAAAACAAAAA ACCAAGAAGTTTGAGACCAGTTTGGGAAACATCGTAAGACCTCATCTCAAAAACAAAAACAAAAA T G TTC28 Ensembl:ENSG00000100154 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1016610935 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 33033 RMVar_ID_33033 Human_SNP_ID_701127828 A-to-I Human chr22 - 28412941 28412941 28412941 ATTTCATTGTGAAAAGGAACATAGATTGTATTAGTGTGAGAGAAGAGGAAACTGAATCCTAAGCA ATTTCATTGTGAAAAGGAACATAGATTGTATTCGTGTGAGAGAAGAGGAAACTGAATCCTAAGCA T G TTC28 Ensembl:ENSG00000100154 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1047987864 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14434571,Human_RBP_ID_25660651 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 33034 RMVar_ID_33034 Human_SNP_ID_701147214 A-to-I Human chr22 - 28499890 28499890 28499890 GATAAATGTTTGAGATGATGAGTATGCTGATTACCCCAATCTGATCACTATACATTATATGTATT GATAAATGTTTGAGATGATGAGTATGCTGATTCCCCCAATCTGATCACTATACATTATATGTATT T G TTC28 Ensembl:ENSG00000100154 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1210825943 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1609436,Human_RBP_ID_14436419,Human_RBP_ID_23940913 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 33035 RMVar_ID_33035 Human_SNP_ID_701149256 A-to-I Human chr22 - 28508929 28508928 28508929 ACCTGGCCTCCCAAAATGCTGGGATTACAGGCATGAGCCACGGTGCCTGGCTTAGGTGGAGAGTT ACCTGGCCTCCCAAAATGCTGGGATTACAGGC_TGAGCCACGGTGCCTGGCTTAGGTGGAGAGTT AT A TTC28 Ensembl:ENSG00000100154 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1489738510 Functional Loss DEL 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_213551,RMVar_hsa_circ_213550 33036 RMVar_ID_33036 Human_SNP_ID_701149257 A-to-I Human chr22 - 28508929 28508929 28508929 ACCTGGCCTCCCAAAATGCTGGGATTACAGGCATGAGCCACGGTGCCTGGCTTAGGTGGAGAGTT ACCTGGCCTCCCAAAATGCTGGGATTACAGGCTTGAGCCACGGTGCCTGGCTTAGGTGGAGAGTT T A TTC28 Ensembl:ENSG00000100154 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388661510 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_213551,RMVar_hsa_circ_213550 33037 RMVar_ID_33037 Human_SNP_ID_701153665 A-to-I Human chr22 - 28528624 28528624 28528624 TCAAGCAGTTCTCGTGCCTTGGCCTCCCGAGTAGCTCGGACTACAAGTGCATGCCACCATTCCCG TCAAGCAGTTCTCGTGCCTTGGCCTCCCGAGTTGCTCGGACTACAAGTGCATGCCACCATTCCCG T A TTC28 Ensembl:ENSG00000100154 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256893993 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_213551,RMVar_hsa_circ_213555,RMVar_hsa_circ_213556 33038 RMVar_ID_33038 Human_SNP_ID_701156873 A-to-I Human chr22 - 28539452 28539452 28539452 TTTGTATATTTTTATAGAGATGGGTTTTCACCATGTTGCTCAGGCTGGTCTGGAACCCCTGGGCT TTTGTATATTTTTATAGAGATGGGTTTTCACCGTGTTGCTCAGGCTGGTCTGGAACCCCTGGGCT T C TTC28 Ensembl:ENSG00000100154 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs767878594 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_213551,RMVar_hsa_circ_213555,RMVar_hsa_circ_213556 33039 RMVar_ID_33039 Human_SNP_ID_701168785 A-to-I Human chr22 - 28589789 28589789 28589789 GTGATCTACCCGCCTTGGCCTCCCAAAGTGCTAGGATTACAGGCGTGAGCCACCATGCCCGACCG GTGATCTACCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCATGCCCGACCG T C TTC28 Ensembl:ENSG00000100154 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1189675006 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 33040 RMVar_ID_33040 Human_SNP_ID_701172245 A-to-I Human chr22 - 28603603 28603603 28603603 ATCGCTTGAGGACAGAAATTTGAGACAAGCCTAGGCAACAAAGCCAGACCCCATCTCTACAAAAA ATCGCTTGAGGACAGAAATTTGAGACAAGCCTCGGCAACAAAGCCAGACCCCATCTCTACAAAAA T G TTC28 Ensembl:ENSG00000100154 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1237762584 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 33041 RMVar_ID_33041 Human_SNP_ID_701172254 A-to-I Human chr22 - 28603650 28603650 28603650 TGGCTCACACTTGTAATCTCAGTGTTTTGGAAAGCCGAGGCAGGAGAATCGCTTGAGGACAGAAA TGGCTCACACTTGTAATCTCAGTGTTTTGGAAGGCCGAGGCAGGAGAATCGCTTGAGGACAGAAA T C TTC28 Ensembl:ENSG00000100154 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1231303734 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7071216,Human_RBP_ID_14438670 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 33042 RMVar_ID_33042 Human_SNP_ID_701177991 A-to-I Human chr22 - 28628718 28628718 28628718 CCAGGCTGGTCTCGAACTCCTGAGCTCAAGCAATCTGCCTGCCTCGGTCTCCCGAAGTGCTGGGA CCAGGCTGGTCTCGAACTCCTGAGCTCAAGCAGTCTGCCTGCCTCGGTCTCCCGAAGTGCTGGGA T C TTC28 Ensembl:ENSG00000100154 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs774620101 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_213560 33043 RMVar_ID_33043 Human_SNP_ID_701194864 A-to-I Human chr22 - 28698332 28698332 28698332 GGAGTCCAATGGCACGATCTCGGCTCACTACAACCTCCACCTCGGGTTCAAGTGATTCTCCTGCC GGAGTCCAATGGCACGATCTCGGCTCACTACAGCCTCCACCTCGGGTTCAAGTGATTCTCCTGCC T C CHEK2 Ensembl:ENSG00000183765 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1174751944 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18786540 RMVar_hsa_circ_46485,RMVar_hsa_circ_283535,RMVar_hsa_circ_65355,RMVar_hsa_circ_298399,RMVar_hsa_circ_347268,RMVar_hsa_circ_213569,RMVar_hsa_circ_64474,RMVar_hsa_circ_38531,RMVar_hsa_circ_339753,RMVar_hsa_circ_43099,RMVar_hsa_circ_350105,RMVar_hsa_circ_350199 33044 RMVar_ID_33044 Human_SNP_ID_701194873 A-to-I Human chr22 - 28698356 28698356 28698356 ATGTCTCACTGTGTCGCCCAGGCTGGAGTCCAATGGCACGATCTCGGCTCACTACAACCTCCACC ATGTCTCACTGTGTCGCCCAGGCTGGAGTCCAGTGGCACGATCTCGGCTCACTACAACCTCCACC T C CHEK2 Ensembl:ENSG00000183765 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs573091387 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14439782 RMVar_hsa_circ_46485,RMVar_hsa_circ_283535,RMVar_hsa_circ_65355,RMVar_hsa_circ_298399,RMVar_hsa_circ_347268,RMVar_hsa_circ_213569,RMVar_hsa_circ_64474,RMVar_hsa_circ_38531,RMVar_hsa_circ_339753,RMVar_hsa_circ_43099,RMVar_hsa_circ_350105,RMVar_hsa_circ_350199 33045 RMVar_ID_33045 Human_SNP_ID_701197025 A-to-I Human chr22 - 28705356 28705356 28705356 AAAAAGATTTTGGGCCGGGTGCAGTGGCTCACACCTGTAATCCCAACACTTTGGGAGGCTGAGGC AAAAAGATTTTGGGCCGGGTGCAGTGGCTCACGCCTGTAATCCCAACACTTTGGGAGGCTGAGGC T C CHEK2 Ensembl:ENSG00000183765 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1311829394 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_46485,RMVar_hsa_circ_298399,RMVar_hsa_circ_347268,RMVar_hsa_circ_14617,RMVar_hsa_circ_38531,RMVar_hsa_circ_43099,RMVar_hsa_circ_350105,RMVar_hsa_circ_344260,RMVar_hsa_circ_350199,RMVar_hsa_circ_345338,RMVar_hsa_circ_281135,RMVar_hsa_circ_289414,RMVar_hsa_circ_213570 33046 RMVar_ID_33046 Human_SNP_ID_701201643 A-to-I Human chr22 - 28722837 28722837 28722837 CGGCATGAGTCTGTAGTCCCTGCTACTCAGAAAGGTGAGGCTAGAGGATCCCTTGAGCCCAGGAT CGGCATGAGTCTGTAGTCCCTGCTACTCAGAAGGGTGAGGCTAGAGGATCCCTTGAGCCCAGGAT T C CHEK2 Ensembl:ENSG00000183765 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1292573028 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38531,RMVar_hsa_circ_43099,RMVar_hsa_circ_350199,RMVar_hsa_circ_345338,RMVar_hsa_circ_281135,RMVar_hsa_circ_213571,RMVar_hsa_circ_289414,RMVar_hsa_circ_213570,RMVar_hsa_circ_349529,RMVar_hsa_circ_295467,RMVar_hsa_circ_318919,RMVar_hsa_circ_334440,RMVar_hsa_circ_274356,RMVar_hsa_circ_213572 33047 RMVar_ID_33047 Human_SNP_ID_701202225 A-to-I Human chr22 - 28724845 28724845 28724845 AGATGAGTAAGTTGCTGGGCGTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGC AGATGAGTAAGTTGCTGGGCGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGC T C CHEK2 Ensembl:ENSG00000183765 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1376629784 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2149704,Human_Splice_Rec_2149824,Human_Splice_Rec_2149840 RMVar_hsa_circ_38531,RMVar_hsa_circ_43099,RMVar_hsa_circ_350199,RMVar_hsa_circ_345338,RMVar_hsa_circ_281135,RMVar_hsa_circ_213571,RMVar_hsa_circ_289414,RMVar_hsa_circ_213570,RMVar_hsa_circ_349529,RMVar_hsa_circ_295467,RMVar_hsa_circ_318919,RMVar_hsa_circ_334440,RMVar_hsa_circ_274356,RMVar_hsa_circ_213572 33048 RMVar_ID_33048 Human_SNP_ID_701205407 A-to-I Human chr22 - 28735284 28735284 28735284 CTCCTGCCTCAGCCTCCCGAGTAGCTGAGAATACAGGTGCCCGCCACCACGCCTGGCTAATTTTT CTCCTGCCTCAGCCTCCCGAGTAGCTGAGAATGCAGGTGCCCGCCACCACGCCTGGCTAATTTTT T C CHEK2 Ensembl:ENSG00000183765 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1477134611 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23941361 33049 RMVar_ID_33049 Human_SNP_ID_701205408 A-to-I Human chr22 - 28735286 28735286 28735286 TTCTCCTGCCTCAGCCTCCCGAGTAGCTGAGAATACAGGTGCCCGCCACCACGCCTGGCTAATTT TTCTCCTGCCTCAGCCTCCCGAGTAGCTGAGAGTACAGGTGCCCGCCACCACGCCTGGCTAATTT T C CHEK2 Ensembl:ENSG00000183765 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1246501689 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23941361 33050 RMVar_ID_33050 Human_SNP_ID_701205522 A-to-I Human chr22 - 28735795 28735795 28735795 TCAGTGCAACCTCTGCCTCCTGGGCTCGAGCAATTCTCCTGCTTCAGCCTCCTGAGTAGCTGGAA TCAGTGCAACCTCTGCCTCCTGGGCTCGAGCAGTTCTCCTGCTTCAGCCTCCTGAGTAGCTGGAA T C CHEK2 Ensembl:ENSG00000183765 Protein coding intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1485552619 Functional Loss SNV dbSNP153 33..33 33 - - - 33051 RMVar_ID_33051 Human_SNP_ID_701205539 A-to-I Human chr22 - 28735877 28735877 28735877 TTATTTATTTAATTAATTAATTTTTTTGAGACAGGGTTTCACTCCTGTCACCCAGGCTGGAGTGC TTATTTATTTAATTAATTAATTTTTTTGAGACGGGGTTTCACTCCTGTCACCCAGGCTGGAGTGC T C CHEK2 Ensembl:ENSG00000183765 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1358107529 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7071565 33052 RMVar_ID_33052 Human_SNP_ID_701206069 A-to-I Human chr22 - 28737949 28737949 28737949 TACCTGCGTTGGCCTCCCAAAGTGCTGGGATTACAGACATGAACCACCACACCTGGCAGAACCTT TACCTGCGTTGGCCTCCCAAAGTGCTGGGATTGCAGACATGAACCACCACACCTGGCAGAACCTT T C CHEK2 Ensembl:ENSG00000183765 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs543853439 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2149612,Human_Splice_Rec_2149613,Human_Splice_Rec_2149932,Human_Splice_Rec_2149933 33053 RMVar_ID_33053 Human_SNP_ID_701206085 A-to-I Human chr22 - 28738014 28738014 28738014 TTCTGTAGATACTGGATTTCACCATGGTGCCCAGGCTGGTCTTGAATTCCTGGGCTCAAGCAATC TTCTGTAGATACTGGATTTCACCATGGTGCCCCGGCTGGTCTTGAATTCCTGGGCTCAAGCAATC T G CHEK2 Ensembl:ENSG00000183765 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs545068493 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2149612,Human_Splice_Rec_2149932,Human_Splice_Rec_2149933 33054 RMVar_ID_33054 Human_SNP_ID_701206108 A-to-I Human chr22 - 28738095 28738095 28738095 TCAAGTGATCCTCCCACCTCAGCTTCCCAAGTAGCTGGGACTACAGGTGCACACCACCATGCCCT TCAAGTGATCCTCCCACCTCAGCTTCCCAAGTCGCTGGGACTACAGGTGCACACCACCATGCCCT T G CHEK2 Ensembl:ENSG00000183765 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946605906 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2149673 33055 RMVar_ID_33055 Human_SNP_ID_701206143 A-to-I Human chr22 - 28738213 28738213 28738213 AGAAAACTCATCAGAACCTTTGTATCTTTTTTATTTTCCTTGAGACAGGGTCTCGCTCTGTCACC AGAAAACTCATCAGAACCTTTGTATCTTTTTTGTTTTCCTTGAGACAGGGTCTCGCTCTGTCACC T C CHEK2 Ensembl:ENSG00000183765 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1288871439 Functional Loss SNV dbSNP153 33..33 33 - - - 33056 RMVar_ID_33056 Human_SNP_ID_701208358 A-to-I Human chr22 + 28746260 28746260 28746260 AAAATTAGCCGGGCGTGGTGGCGGGTGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTAGCCGGGCGTGGTGGCGGGTGCCTGTGGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA A G HSCB Ensembl:ENSG00000100209 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs539333829 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61116,RMVar_hsa_circ_350624,RMVar_hsa_circ_213577,RMVar_hsa_circ_375326 33057 RMVar_ID_33057 Human_SNP_ID_701208604 A-to-I Human chr22 + 28746984 28746984 28746984 TATTCAGGAGGATGAGGTGGGAGAATCATCTGAGCCCAGGAGGCAGAGGTTGCAGTGAGCTGAGA TATTCAGGAGGATGAGGTGGGAGAATCATCTGCGCCCAGGAGGCAGAGGTTGCAGTGAGCTGAGA A C HSCB Ensembl:ENSG00000100209 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1199814569 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61116,RMVar_hsa_circ_350624,RMVar_hsa_circ_213577,RMVar_hsa_circ_375326 33058 RMVar_ID_33058 Human_SNP_ID_701208722 A-to-I Human chr22 + 28747530 28747530 28747530 CACCATGTTGCCCAGGCTGGCTTCAAACTCCTAGGTTCAAAGCAATCCACCTTCCTCAGTCTCCC CACCATGTTGCCCAGGCTGGCTTCAAACTCCTGGGTTCAAAGCAATCCACCTTCCTCAGTCTCCC A G HSCB Ensembl:ENSG00000100209 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1313388888 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61116,RMVar_hsa_circ_350624,RMVar_hsa_circ_213577,RMVar_hsa_circ_375326 33059 RMVar_ID_33059 Human_SNP_ID_701208877 A-to-I Human chr22 + 28748150 28748150 28748150 GAGGTTGCAGTGAGCCGAGATTGTGCCACTGCACTCCAGCCTGAGTGACAGAGCGAGACTCCGAA GAGGTTGCAGTGAGCCGAGATTGTGCCACTGCTCTCCAGCCTGAGTGACAGAGCGAGACTCCGAA A T HSCB Ensembl:ENSG00000100209 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1422310499 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61116,RMVar_hsa_circ_350624,RMVar_hsa_circ_213577,RMVar_hsa_circ_375326 33060 RMVar_ID_33060 Human_SNP_ID_701209015 A-to-I Human chr22 + 28748606 28748606 28748606 ATGATCTCGGCTCACTGCAACCTCCGCCTCCCAGGTTCCAGCTATTCTCCTGCCTCTGCCTCCCA ATGATCTCGGCTCACTGCAACCTCCGCCTCCCGGGTTCCAGCTATTCTCCTGCCTCTGCCTCCCA A G HSCB Ensembl:ENSG00000100209 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1315202356 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61116,RMVar_hsa_circ_350624,RMVar_hsa_circ_213577,RMVar_hsa_circ_375326 33061 RMVar_ID_33061 Human_SNP_ID_701209029 A-to-I Human chr22 + 28748654 28748654 28748654 CCTGCCTCTGCCTCCCAAGTAGCTGGGACTACAGGTGCGTGCCACCATGCTTGGCTAATTTTTCT CCTGCCTCTGCCTCCCAAGTAGCTGGGACTACGGGTGCGTGCCACCATGCTTGGCTAATTTTTCT A G HSCB Ensembl:ENSG00000100209 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs147173343 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61116,RMVar_hsa_circ_350624,RMVar_hsa_circ_213577,RMVar_hsa_circ_375326 33062 RMVar_ID_33062 Human_SNP_ID_701216618 A-to-I Human chr22 + 28774585 28774585 28774585 TTTTGTAGAGATGGTGTCTCACTATGTTGCCCAGTCTGGTCATGAACTTCTGGCCTCAAGCAGTC TTTTGTAGAGATGGTGTCTCACTATGTTGCCCCGTCTGGTCATGAACTTCTGGCCTCAAGCAGTC A C CCDC117 Ensembl:ENSG00000159873 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1209086645 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14440371 RMVar_hsa_circ_86892,RMVar_hsa_circ_122956,RMVar_hsa_circ_213578,RMVar_hsa_circ_213579 33063 RMVar_ID_33063 Human_SNP_ID_701216781 A-to-I Human chr22 + 28775154 28775154 28775154 GTAGTGGTGCGTAACTGTAATGCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCCG GTAGTGGTGCGTAACTGTAATGCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCCG A G CCDC117 Ensembl:ENSG00000159873 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1400474234 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86892,RMVar_hsa_circ_122956,RMVar_hsa_circ_213578,RMVar_hsa_circ_213579 33064 RMVar_ID_33064 Human_SNP_ID_701217801 A-to-I Human chr22 + 28778497 28778497 28778497 GGGCGTGGTGGTGCGCACCTGTAGTCCCAGCTACTCGGGGGGCTGAGGCGGGAGAATTGCTTGAA GGGCGTGGTGGTGCGCACCTGTAGTCCCAGCTCCTCGGGGGGCTGAGGCGGGAGAATTGCTTGAA A C CCDC117 Ensembl:ENSG00000159873 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1455545154 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86892,RMVar_hsa_circ_122956,RMVar_hsa_circ_213578,RMVar_hsa_circ_213579 33065 RMVar_ID_33065 Human_SNP_ID_701223378 A-to-I Human chr22 - 28798401 28798401 28798401 CGGAGGCTGACGCAGGAGAATCACTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCTGAGATCACG CGGAGGCTGACGCAGGAGAATCACTTGAACCCGGGAGGCGGAGGTTGCAGTGAGCTGAGATCACG T C XBP1 Ensembl:ENSG00000100219 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1048850301 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110299,RMVar_hsa_circ_100890,RMVar_hsa_circ_213581,RMVar_hsa_circ_213582,RMVar_hsa_circ_64989,RMVar_hsa_circ_354892 33066 RMVar_ID_33066 Human_SNP_ID_701223379 A-to-I Human chr22 - 28798401 28798401 28798401 CGGAGGCTGACGCAGGAGAATCACTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCTGAGATCACG CGGAGGCTGACGCAGGAGAATCACTTGAACCCCGGAGGCGGAGGTTGCAGTGAGCTGAGATCACG T G XBP1 Ensembl:ENSG00000100219 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1048850301 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110299,RMVar_hsa_circ_100890,RMVar_hsa_circ_213581,RMVar_hsa_circ_213582,RMVar_hsa_circ_64989,RMVar_hsa_circ_354892 33067 RMVar_ID_33067 Human_SNP_ID_701225022 A-to-I Human chr22 + 28804040 28804039 28804041 AAAATTAACCAGGCGTGGTGACTTGCACCTGTAGTCCCAGCTGCTCGGAAGACGGAGGTGGTAAG AAAATTAACCAGGCGTGGTGACTTGCACCTGT__TCCCAGCTGCTCGGAAGACGGAGGTGGTAAG TAG T Z93930.2 Ensembl:ENSG00000226471 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904147607 Functional Loss DEL dbSNP153 33..34 33 - - - 33068 RMVar_ID_33068 Human_SNP_ID_701225628 A-to-I Human chr22 + 28806310 28806310 28806310 TGCCACCATACCCATCTAATTTTTGTTTTTTTAGTAGAGACGGTTTCACCATGTTGGACAGGCTG TGCCACCATACCCATCTAATTTTTGTTTTTTTTGTAGAGACGGTTTCACCATGTTGGACAGGCTG A T Z93930.2 Ensembl:ENSG00000226471 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1359454709 Functional Loss SNV dbSNP153 33..33 33 - - - 33069 RMVar_ID_33069 Human_SNP_ID_701225647 A-to-I Human chr22 + 28806400 28806400 28806400 CGCCCGCCTCGGCCTCCCAAAGTGTTGGGATTACAGGTGTGAGCCACTGTGCCCAGACAGGCCTA CGCCCGCCTCGGCCTCCCAAAGTGTTGGGATTTCAGGTGTGAGCCACTGTGCCCAGACAGGCCTA A T Z93930.2 Ensembl:ENSG00000226471 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs377196085 Functional Loss SNV dbSNP153 33..33 33 - - - 33070 RMVar_ID_33070 Human_SNP_ID_701227026 A-to-I Human chr22 + 28812514 28812514 28812514 TCAAGTGATTCTCCTGGGTCAGCCTCCTGAGTAGCTGAGACTACAGGCACCTGCCACCATGCCCG TCAAGTGATTCTCCTGGGTCAGCCTCCTGAGTGGCTGAGACTACAGGCACCTGCCACCATGCCCG A G Z93930.2 Ensembl:ENSG00000226471 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs938588073 Functional Loss SNV dbSNP153 33..33 33 - - - 33071 RMVar_ID_33071 Human_SNP_ID_701234561 A-to-I Human chr22 + 28844354 28844354 28844354 AGCTGGCTGCAGTGAGCTATGATCACACCACTACTCTCCAGCCTAGGTGACACAGCAAGACTCTG AGCTGGCTGCAGTGAGCTATGATCACACCACTGCTCTCCAGCCTAGGTGACACAGCAAGACTCTG A G Z93930.2 Ensembl:ENSG00000226471 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs929822683 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_213587 33072 RMVar_ID_33072 Human_SNP_ID_701235032 A-to-I Human chr22 + 28845404 28845404 28845404 GTGAGCCCAGGAATTCGAGGCTGCAATGAGCCATGATTGAGAGACTGCACTCTAGCCTGGTCGAC GTGAGCCCAGGAATTCGAGGCTGCAATGAGCCCTGATTGAGAGACTGCACTCTAGCCTGGTCGAC A C Z93930.2 Ensembl:ENSG00000226471 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs979436590 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_213587 33073 RMVar_ID_33073 Human_SNP_ID_701235033 A-to-I Human chr22 + 28845404 28845404 28845404 GTGAGCCCAGGAATTCGAGGCTGCAATGAGCCATGATTGAGAGACTGCACTCTAGCCTGGTCGAC GTGAGCCCAGGAATTCGAGGCTGCAATGAGCCGTGATTGAGAGACTGCACTCTAGCCTGGTCGAC A G Z93930.2 Ensembl:ENSG00000226471 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs979436590 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_213587 33074 RMVar_ID_33074 Human_SNP_ID_701236504 A-to-I Human chr22 + 28851362 28851362 28851362 GGGCATGGTGGAATGCGCCTGTAATCCCAGCTACTTGAGAGGTTGAGGCGGGAGAATTGCTTGAA GGGCATGGTGGAATGCGCCTGTAATCCCAGCTGCTTGAGAGGTTGAGGCGGGAGAATTGCTTGAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1327800056 Functional Loss SNV dbSNP153 33..33 33 - - - 33075 RMVar_ID_33075 Human_SNP_ID_701246544 A-to-I Human chr22 + 28890806 28890806 28890806 TTTTGTCAGGGTCTCACCATGTTGCCCAGGCTAGAGCACAGTGGTAAGATCATGGCTCAGTGTAC TTTTGTCAGGGTCTCACCATGTTGCCCAGGCTGGAGCACAGTGGTAAGATCATGGCTCAGTGTAC A G ZNRF3 Ensembl:ENSG00000183579 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1046804350 Functional Loss SNV dbSNP153 33..33 33 - - - 33076 RMVar_ID_33076 Human_SNP_ID_701246549 A-to-I Human chr22 + 28890832 28890831 28890832 CAGGCTAGAGCACAGTGGTAAGATCATGGCTCAGTGTACTCTTGGACTCCTGGGCTCAGGCAGTT CAGGCTAGAGCACAGTGGTAAGATCATGGCTC_GTGTACTCTTGGACTCCTGGGCTCAGGCAGTT CA C ZNRF3 Ensembl:ENSG00000183579 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417885148 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_14441208 33077 RMVar_ID_33077 Human_SNP_ID_701247187 A-to-I Human chr22 + 28893698 28893698 28893698 GTTTGTATTTTCTGTAGAGATGGGGTTTCCCCATGTTGCTCAGGCTGGTCTTGAACTTGGGAGCT GTTTGTATTTTCTGTAGAGATGGGGTTTCCCCGTGTTGCTCAGGCTGGTCTTGAACTTGGGAGCT A G ZNRF3 Ensembl:ENSG00000183579 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444823171 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14441296 33078 RMVar_ID_33078 Human_SNP_ID_701324522 A-to-I Human chr22 + 29219598 29219598 29219598 GGCCAGAAGTTCAAGCCTAGCCTGGGCAACATAGCAAGACCCTATCTCAAAAAAAAAAGTTAAAA GGCCAGAAGTTCAAGCCTAGCCTGGGCAACATTGCAAGACCCTATCTCAAAAAAAAAAGTTAAAA A T EMID1 Ensembl:ENSG00000186998 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1358058033 Functional Loss SNV dbSNP153 33..33 33 - - - 33079 RMVar_ID_33079 Human_SNP_ID_701326545 A-to-I Human chr22 + 29227114 29227114 29227114 TTGTGTATTTTTTGTTTTGTTTTGTTTGAAACAGGGTCTTCCTCTGTTGCCCAGGCTGGAGTGCA TTGTGTATTTTTTGTTTTGTTTTGTTTGAAACCGGGTCTTCCTCTGTTGCCCAGGCTGGAGTGCA A C EMID1 Ensembl:ENSG00000186998 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs766677379 Functional Loss SNV dbSNP153 33..33 33 - - - 33080 RMVar_ID_33080 Human_SNP_ID_701326554 A-to-I Human chr22 + 29227203 29227203 29227203 ACCTATGCCTCCTGGGCTCAAATGATCCTCCCACCTCAGCCTCCTGAGTAGCTGGGACCATAGGT ACCTATGCCTCCTGGGCTCAAATGATCCTCCCCCCTCAGCCTCCTGAGTAGCTGGGACCATAGGT A C EMID1 Ensembl:ENSG00000186998 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1229113192 Functional Loss SNV dbSNP153 33..33 33 - - - 33081 RMVar_ID_33081 Human_SNP_ID_701326575 A-to-I Human chr22 + 29227319 29227319 29227319 CTCCATGTTGCCCAGGCTGGTCTTGAACTTCTAAGCTCAAGCAATTCACTGTCTTGGCCTCCCAA CTCCATGTTGCCCAGGCTGGTCTTGAACTTCTGAGCTCAAGCAATTCACTGTCTTGGCCTCCCAA A G EMID1 Ensembl:ENSG00000186998 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs560886275 Functional Loss SNV dbSNP153 33..33 33 - - - 33082 RMVar_ID_33082 Human_SNP_ID_701326991 A-to-I Human chr22 + 29228699 29228699 29228699 TCACTGCAGCCTCCAATTCCTGGGCTCAAGCTATCCTCCTGCCCCAACCTCCTGAGTAGCTGGCA TCACTGCAGCCTCCAATTCCTGGGCTCAAGCTGTCCTCCTGCCCCAACCTCCTGAGTAGCTGGCA A G EMID1 Ensembl:ENSG00000186998 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs953521206 Functional Loss SNV dbSNP153 33..33 33 - - - 33083 RMVar_ID_33083 Human_SNP_ID_701326992 A-to-I Human chr22 + 29228699 29228699 29228699 TCACTGCAGCCTCCAATTCCTGGGCTCAAGCTATCCTCCTGCCCCAACCTCCTGAGTAGCTGGCA TCACTGCAGCCTCCAATTCCTGGGCTCAAGCTTTCCTCCTGCCCCAACCTCCTGAGTAGCTGGCA A T EMID1 Ensembl:ENSG00000186998 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs953521206 Functional Loss SNV dbSNP153 33..33 33 - - - 33084 RMVar_ID_33084 Human_SNP_ID_701327012 A-to-I Human chr22 + 29228779 29228779 29228779 ACCACACCTGGCTAGTTTAAAAAACTTTTTTTAGAGCTGGGGTCTTGCTATGTTTCCTAAACTGG ACCACACCTGGCTAGTTTAAAAAACTTTTTTTTGAGCTGGGGTCTTGCTATGTTTCCTAAACTGG A T EMID1 Ensembl:ENSG00000186998 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs574466448 Functional Loss SNV dbSNP153 33..33 33 - - - 33085 RMVar_ID_33085 Human_SNP_ID_701327021 A-to-I Human chr22 + 29228805 29228805 29228805 TTTTTTAGAGCTGGGGTCTTGCTATGTTTCCTAAACTGGTCCTGAACTCTTGGCCTCAAGGAATC TTTTTTAGAGCTGGGGTCTTGCTATGTTTCCTGAACTGGTCCTGAACTCTTGGCCTCAAGGAATC A G EMID1 Ensembl:ENSG00000186998 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1455224560 Functional Loss SNV dbSNP153 33..33 33 - - - 33086 RMVar_ID_33086 Human_SNP_ID_701327087 A-to-I Human chr22 + 29229155 29229155 29229155 CTTGAGGCCTGGAGCCCGAGACCAGCCTGGGCAACATAGCAAGACTCCATCTCTACAAAAAATTA CTTGAGGCCTGGAGCCCGAGACCAGCCTGGGCGACATAGCAAGACTCCATCTCTACAAAAAATTA A G EMID1 Ensembl:ENSG00000186998 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs988668009 Functional Loss SNV dbSNP153 33..33 33 - - - 33087 RMVar_ID_33087 Human_SNP_ID_701327498 A-to-I Human chr22 + 29230723 29230723 29230723 CCTGTAATCCCAACACTTTGGGAGGCTGAGGCAAGATGATTGCTTGAGCCCAGGAGTTCAAGACC CCTGTAATCCCAACACTTTGGGAGGCTGAGGCGAGATGATTGCTTGAGCCCAGGAGTTCAAGACC A G EMID1 Ensembl:ENSG00000186998 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1050850976 Functional Loss SNV dbSNP153 33..33 33 - - - 33088 RMVar_ID_33088 Human_SNP_ID_701327528 A-to-I Human chr22 + 29230804 29230804 29230804 CGAGACCTCGTCTCTACAAATAATTTTTTTTTAAATTTGCCATGTGTGGTGGTGCATCCCTGTGG CGAGACCTCGTCTCTACAAATAATTTTTTTTTTAATTTGCCATGTGTGGTGGTGCATCCCTGTGG A T EMID1 Ensembl:ENSG00000186998 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs3765295 Functional Loss SNV dbSNP153 33..33 33 - - - 33089 RMVar_ID_33089 Human_SNP_ID_701327533 A-to-I Human chr22 + 29230813 29230812 29230814 GTCTCTACAAATAATTTTTTTTTAAATTTGCCATGTGTGGTGGTGCATCCCTGTGGTCCCAGCTA GTCTCTACAAATAATTTTTTTTTAAATTTGCC__GTGTGGTGGTGCATCCCTGTGGTCCCAGCTA CAT C EMID1 Ensembl:ENSG00000186998 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1317579239 Functional Loss DEL dbSNP153 33..34 33 - - - 33090 RMVar_ID_33090 Human_SNP_ID_701327534 A-to-I Human chr22 + 29230813 29230813 29230813 GTCTCTACAAATAATTTTTTTTTAAATTTGCCATGTGTGGTGGTGCATCCCTGTGGTCCCAGCTA GTCTCTACAAATAATTTTTTTTTAAATTTGCCGTGTGTGGTGGTGCATCCCTGTGGTCCCAGCTA A G EMID1 Ensembl:ENSG00000186998 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs3765296 Functional Loss SNV dbSNP153,JSNP 33..33 33 - - - 33091 RMVar_ID_33091 Human_SNP_ID_701335577 A-to-I Human chr22 - 29261362 29261362 29261362 GAACTCCTGGCCTCAAGTGATCCTCCCGTCTCAGCCTCCCCAAGTGCTGGGATTATACAGCTGTG GAACTCCTGGCCTCAAGTGATCCTCCCGTCTCGGCCTCCCCAAGTGCTGGGATTATACAGCTGTG T C RHBDD3 Ensembl:ENSG00000100263 Protein coding intron GSE100210;GSE99789 HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 29129909,29796672 RNA-Seq:(High) rs1271478000 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2150400 RMVar_hsa_circ_72363 33092 RMVar_ID_33092 Human_SNP_ID_701341072 A-to-I Human chr22 + 29278934 29278934 29278934 GGAGAATTACTTGAACCTGGGAGATGGAGGTTACAGTGAGCTAAGATGGCACCATTGTACTCTAG GGAGAATTACTTGAACCTGGGAGATGGAGGTTGCAGTGAGCTAAGATGGCACCATTGTACTCTAG A G EWSR1 Ensembl:ENSG00000182944 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1258028388 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14444126,Human_RBP_ID_23311989 RMVar_hsa_circ_113042,RMVar_hsa_circ_87238,RMVar_hsa_circ_103154,RMVar_hsa_circ_213608,RMVar_hsa_circ_213609,RMVar_hsa_circ_105688,RMVar_hsa_circ_115792,RMVar_hsa_circ_213611,RMVar_hsa_circ_213612,RMVar_hsa_circ_38608,RMVar_hsa_circ_348722,RMVar_hsa_circ_213613,RMVar_hsa_circ_325413 33093 RMVar_ID_33093 Human_SNP_ID_701341075 A-to-I Human chr22 + 29278952 29278952 29278952 GGGAGATGGAGGTTACAGTGAGCTAAGATGGCACCATTGTACTCTAGCCTGGGCGACAGAGGAAG GGGAGATGGAGGTTACAGTGAGCTAAGATGGCCCCATTGTACTCTAGCCTGGGCGACAGAGGAAG A C EWSR1 Ensembl:ENSG00000182944 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs958673559 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14444126,Human_RBP_ID_23012061,Human_RBP_ID_25681851 RMVar_hsa_circ_113042,RMVar_hsa_circ_87238,RMVar_hsa_circ_103154,RMVar_hsa_circ_213608,RMVar_hsa_circ_213609,RMVar_hsa_circ_105688,RMVar_hsa_circ_115792,RMVar_hsa_circ_213611,RMVar_hsa_circ_213612,RMVar_hsa_circ_38608,RMVar_hsa_circ_348722,RMVar_hsa_circ_213613,RMVar_hsa_circ_325413 33094 RMVar_ID_33094 Human_SNP_ID_701341622 A-to-I Human chr22 + 29280691 29280691 29280691 TGGATGGTTTGGTTGGTTTTTTTTTTTTTTTTAAGATGGAGTTTTGCTCTTGTTGTCCAGGCTAG TGGATGGTTTGGTTGGTTTTTTTTTTTTTTTTTAGATGGAGTTTTGCTCTTGTTGTCCAGGCTAG A T EWSR1 Ensembl:ENSG00000182944 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1352103869 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113042,RMVar_hsa_circ_87238,RMVar_hsa_circ_103154,RMVar_hsa_circ_213608,RMVar_hsa_circ_213609,RMVar_hsa_circ_105688,RMVar_hsa_circ_115792,RMVar_hsa_circ_213611,RMVar_hsa_circ_213612,RMVar_hsa_circ_38608,RMVar_hsa_circ_348722,RMVar_hsa_circ_213613,RMVar_hsa_circ_325413 33095 RMVar_ID_33095 Human_SNP_ID_701341850 A-to-I Human chr22 + 29281095 29281095 29281095 TAGAGACAGGGTTTCACTGTGTTTGCCAGGATAGTCTCGATCTCCTGACCTCGTGATCCTCCTGT TAGAGACAGGGTTTCACTGTGTTTGCCAGGATGGTCTCGATCTCCTGACCTCGTGATCCTCCTGT A G EWSR1 Ensembl:ENSG00000182944 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1366148809 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14444232,Human_RBP_ID_25663164 RMVar_hsa_circ_113042,RMVar_hsa_circ_87238,RMVar_hsa_circ_103154,RMVar_hsa_circ_213608,RMVar_hsa_circ_213609,RMVar_hsa_circ_105688,RMVar_hsa_circ_115792,RMVar_hsa_circ_213611,RMVar_hsa_circ_213612,RMVar_hsa_circ_38608,RMVar_hsa_circ_348722,RMVar_hsa_circ_213613,RMVar_hsa_circ_325413 33096 RMVar_ID_33096 Human_SNP_ID_701341865 A-to-I Human chr22 + 29281131 29281131 29281131 TCGATCTCCTGACCTCGTGATCCTCCTGTCTCAGCCTCCCAAAGTTCTGGGATTATAGGTGTGAA TCGATCTCCTGACCTCGTGATCCTCCTGTCTCCGCCTCCCAAAGTTCTGGGATTATAGGTGTGAA A C EWSR1 Ensembl:ENSG00000182944 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs985548521 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14444232 RMVar_hsa_circ_113042,RMVar_hsa_circ_87238,RMVar_hsa_circ_103154,RMVar_hsa_circ_213608,RMVar_hsa_circ_213609,RMVar_hsa_circ_105688,RMVar_hsa_circ_115792,RMVar_hsa_circ_213611,RMVar_hsa_circ_213612,RMVar_hsa_circ_38608,RMVar_hsa_circ_348722,RMVar_hsa_circ_213613,RMVar_hsa_circ_325413 33097 RMVar_ID_33097 Human_SNP_ID_701341876 A-to-I Human chr22 + 29281175 29281174 29281175 TTCTGGGATTATAGGTGTGAACCACCGCTACCAGCCAATTTTTTGTATTTCTAGTAGAGACGGGG TTCTGGGATTATAGGTGTGAACCACCGCTACTGGCCAATTTTTTGTATTTCTAGTAGAGACGGGG CA TG EWSR1 Ensembl:ENSG00000182944 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs386820574 Functional Loss MNV dbSNP153 32..33 33 - - - RMVar_hsa_circ_113042,RMVar_hsa_circ_87238,RMVar_hsa_circ_103154,RMVar_hsa_circ_213608,RMVar_hsa_circ_213609,RMVar_hsa_circ_105688,RMVar_hsa_circ_115792,RMVar_hsa_circ_213611,RMVar_hsa_circ_213612,RMVar_hsa_circ_38608,RMVar_hsa_circ_348722,RMVar_hsa_circ_213613,RMVar_hsa_circ_325413 33098 RMVar_ID_33098 Human_SNP_ID_701341879 A-to-I Human chr22 + 29281175 29281175 29281175 TTCTGGGATTATAGGTGTGAACCACCGCTACCAGCCAATTTTTTGTATTTCTAGTAGAGACGGGG TTCTGGGATTATAGGTGTGAACCACCGCTACCGGCCAATTTTTTGTATTTCTAGTAGAGACGGGG A G EWSR1 Ensembl:ENSG00000182944 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs5997460 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113042,RMVar_hsa_circ_87238,RMVar_hsa_circ_103154,RMVar_hsa_circ_213608,RMVar_hsa_circ_213609,RMVar_hsa_circ_105688,RMVar_hsa_circ_115792,RMVar_hsa_circ_213611,RMVar_hsa_circ_213612,RMVar_hsa_circ_38608,RMVar_hsa_circ_348722,RMVar_hsa_circ_213613,RMVar_hsa_circ_325413 33099 RMVar_ID_33099 Human_SNP_ID_701341880 A-to-I Human chr22 + 29281175 29281175 29281175 TTCTGGGATTATAGGTGTGAACCACCGCTACCAGCCAATTTTTTGTATTTCTAGTAGAGACGGGG TTCTGGGATTATAGGTGTGAACCACCGCTACCTGCCAATTTTTTGTATTTCTAGTAGAGACGGGG A T EWSR1 Ensembl:ENSG00000182944 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs5997460 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113042,RMVar_hsa_circ_87238,RMVar_hsa_circ_103154,RMVar_hsa_circ_213608,RMVar_hsa_circ_213609,RMVar_hsa_circ_105688,RMVar_hsa_circ_115792,RMVar_hsa_circ_213611,RMVar_hsa_circ_213612,RMVar_hsa_circ_38608,RMVar_hsa_circ_348722,RMVar_hsa_circ_213613,RMVar_hsa_circ_325413 33100 RMVar_ID_33100 Human_SNP_ID_701341975 A-to-I Human chr22 + 29281508 29281508 29281508 TTTCTATTTCTGTAGAGGTGGGGTCTCCCTATATTACCAGGCTGGTCTGAAACTCCTGGGCTCAA TTTCTATTTCTGTAGAGGTGGGGTCTCCCTATGTTACCAGGCTGGTCTGAAACTCCTGGGCTCAA A G EWSR1 Ensembl:ENSG00000182944 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1290963548 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1307364,Human_RBP_ID_7072501,Human_RBP_ID_14444251,Human_RBP_ID_18445289 RMVar_hsa_circ_113042,RMVar_hsa_circ_87238,RMVar_hsa_circ_103154,RMVar_hsa_circ_213608,RMVar_hsa_circ_213609,RMVar_hsa_circ_105688,RMVar_hsa_circ_115792,RMVar_hsa_circ_213611,RMVar_hsa_circ_213612,RMVar_hsa_circ_38608,RMVar_hsa_circ_348722,RMVar_hsa_circ_213613,RMVar_hsa_circ_325413 33101 RMVar_ID_33101 Human_SNP_ID_701345258 A-to-I Human chr22 + 29292820 29292820 29292820 GAGTTTCCTTCTTGGTGCCCAGGCTGGAGTGCAATGGCGCAAGTCTTGGCTCACTGCAACCTCTG GAGTTTCCTTCTTGGTGCCCAGGCTGGAGTGCGATGGCGCAAGTCTTGGCTCACTGCAACCTCTG A G EWSR1 Ensembl:ENSG00000182944 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs950588390 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14444851 RMVar_hsa_circ_38608 33102 RMVar_ID_33102 Human_SNP_ID_701345312 A-to-I Human chr22 + 29293012 29293012 29293012 CCTCAGGTGATCTGCCCACCTTGGCGCCTCCCAAAGTGCTGGGATTACAGGTGTGATCCCCTACG CCTCAGGTGATCTGCCCACCTTGGCGCCTCCCGAAGTGCTGGGATTACAGGTGTGATCCCCTACG A G EWSR1 Ensembl:ENSG00000182944 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs910308429 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38608 33103 RMVar_ID_33103 Human_SNP_ID_701345553 A-to-I Human chr22 + 29293848 29293848 29293848 GCCTCAACTCCCAAAGTTTTGTGATTGCAGACATGAGCCACTGTGCCTGGCCTGTCTCTATTTGT GCCTCAACTCCCAAAGTTTTGTGATTGCAGACGTGAGCCACTGTGCCTGGCCTGTCTCTATTTGT A G EWSR1 Ensembl:ENSG00000182944 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs140064 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10048797,Human_RBP_ID_14444902,Human_RBP_ID_23012226,Human_RBP_ID_23186586,Human_RBP_ID_25663491 RMVar_hsa_circ_38608 33104 RMVar_ID_33104 Human_SNP_ID_701345874 A-to-I Human chr22 + 29294802 29294802 29294802 CGGGTGTGGTGACACGCGCCTGTAGTTGAGCTACTTGGGAGTCTGAGGCAGGAGAATCAGTTGAT CGGGTGTGGTGACACGCGCCTGTAGTTGAGCTCCTTGGGAGTCTGAGGCAGGAGAATCAGTTGAT A C EWSR1 Ensembl:ENSG00000182944 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs78870312 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7072692,Human_RBP_ID_14444933 RMVar_hsa_circ_38608 33105 RMVar_ID_33105 Human_SNP_ID_701345875 A-to-I Human chr22 + 29294802 29294802 29294802 CGGGTGTGGTGACACGCGCCTGTAGTTGAGCTACTTGGGAGTCTGAGGCAGGAGAATCAGTTGAT CGGGTGTGGTGACACGCGCCTGTAGTTGAGCTGCTTGGGAGTCTGAGGCAGGAGAATCAGTTGAT A G EWSR1 Ensembl:ENSG00000182944 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs78870312 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7072692,Human_RBP_ID_14444933 RMVar_hsa_circ_38608 33106 RMVar_ID_33106 Human_SNP_ID_701345890 A-to-I Human chr22 + 29294845 29294845 29294845 TGAGGCAGGAGAATCAGTTGATCCCAGGATGCAGAGGTTGCAGTGAGCTGAGATGGCGCCACTGC TGAGGCAGGAGAATCAGTTGATCCCAGGATGCGGAGGTTGCAGTGAGCTGAGATGGCGCCACTGC A G EWSR1 Ensembl:ENSG00000182944 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs60983052 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14444933 RMVar_hsa_circ_38608 33107 RMVar_ID_33107 Human_SNP_ID_701345968 A-to-I Human chr22 + 29295127 29295127 29295127 TTGCTCTGTTGCCCAGACTGGAGTGCAGTGGCACAATTTCAGCTCACTGCAACCTCCGCCTCCTG TTGCTCTGTTGCCCAGACTGGAGTGCAGTGGCTCAATTTCAGCTCACTGCAACCTCCGCCTCCTG A T EWSR1 Ensembl:ENSG00000182944 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1255377442 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38608 33108 RMVar_ID_33108 Human_SNP_ID_701346486 A-to-I Human chr22 + 29296984 29296984 29296984 GGTGGGAGGATCACTTGAGCCCGGAGAGTTTGAAGCTCCAGTGAGCTGAGATTGCACCACTGCAC GGTGGGAGGATCACTTGAGCCCGGAGAGTTTGCAGCTCCAGTGAGCTGAGATTGCACCACTGCAC A C EWSR1 Ensembl:ENSG00000182944 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs946068839 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38608,RMVar_hsa_circ_53612 33109 RMVar_ID_33109 Human_SNP_ID_701366356 A-to-I Human chr22 - 29367272 29367261 29367272 ACTGAAAGTCACCCCTCTCTTCTCTCTCTTGCAGAAGCCTGGCTACAGATAAGGGACCAAAATGA ACTGAAAGTCACCCCTCTCTTCTCTCTCTTGC___________TACAGATAAGGGACCAAAATGA AGCCAGGCTTCT A AP1B1 Ensembl:ENSG00000100280 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs765794008 Functional Loss DEL dbSNP153 33..43 33 - - - Human_RBP_ID_4708542 Human_Splice_Rec_2150917,Human_Splice_Rec_2150957,Human_Splice_Rec_2150999,Human_Splice_Rec_2151043,Human_Splice_Rec_2151081,Human_Splice_Rec_2151167,Human_Splice_Rec_2151197 RMVar_hsa_circ_317152 33110 RMVar_ID_33110 Human_SNP_ID_701366362 A-to-I Human chr22 - 29367272 29367272 29367272 ACTGAAAGTCACCCCTCTCTTCTCTCTCTTGCAGAAGCCTGGCTACAGATAAGGGACCAAAATGA ACTGAAAGTCACCCCTCTCTTCTCTCTCTTGCGGAAGCCTGGCTACAGATAAGGGACCAAAATGA T C AP1B1 Ensembl:ENSG00000100280 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1451421587 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4708542 Human_Splice_Rec_2150917,Human_Splice_Rec_2150957,Human_Splice_Rec_2150999,Human_Splice_Rec_2151043,Human_Splice_Rec_2151081,Human_Splice_Rec_2151167,Human_Splice_Rec_2151197 RMVar_hsa_circ_317152 33111 RMVar_ID_33111 Human_SNP_ID_701383827 A-to-I Human chr22 - 29439475 29439475 29439475 GCACCCACCACCAAGCCTGGCTAATTTTTTGTATTTTTAGTAGAGACAGGGTTTCACCGTGTTAT GCACCCACCACCAAGCCTGGCTAATTTTTTGTGTTTTTAGTAGAGACAGGGTTTCACCGTGTTAT T C RFPL1S Ensembl:ENSG00000225465 lincRNA exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1182958149 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_152648 33112 RMVar_ID_33112 Human_SNP_ID_701384139 A-to-I Human chr22 - 29440847 29440847 29440847 TTGTTGGCTGAGCGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGACGGGTGGA TTGTTGGCTGAGCGCGGTGGCTCACACCTGTATTCCCAGCACTTTGGGAGGCCGAGACGGGTGGA T A RFPL1S Ensembl:ENSG00000225465 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1422752790 Functional Loss SNV dbSNP153 33..33 33 - - - 33113 RMVar_ID_33113 Human_SNP_ID_701400346 A-to-I Human chr22 - 29499578 29499578 29499578 TTTATTATTATTACTTTTTGAGATGGAGTCTCACTCTGTTGCCGAGGCTGGAGTGCAGTGGCGTG TTTATTATTATTACTTTTTGAGATGGAGTCTCGCTCTGTTGCCGAGGCTGGAGTGCAGTGGCGTG T C lnc-THOC5-3 RNACentral:URS0000D58030 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1248044813 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14445865 33114 RMVar_ID_33114 Human_SNP_ID_701400560 A-to-I Human chr22 - 29500542 29500542 29500542 TTATTGATTTGAGATCATTCTTCTTTTCCTTTATTTATTTATTTAGAGACAGGGTCTTGCTCTGT TTATTGATTTGAGATCATTCTTCTTTTCCTTTGTTTATTTATTTAGAGACAGGGTCTTGCTCTGT T C lnc-THOC5-3 RNACentral:URS0000D58030 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1455341349 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7072883,Human_RBP_ID_8117123,Human_RBP_ID_14445911 33115 RMVar_ID_33115 Human_SNP_ID_701401208 A-to-I Human chr22 - 29502908 29502908 29502908 GCATAATTGTAGTCCCAGCTACTCAGAAGGCAAAGGCAGGAGGATCACATGAGCCCAGAAGTTGG GCATAATTGTAGTCCCAGCTACTCAGAAGGCAGAGGCAGGAGGATCACATGAGCCCAGAAGTTGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs576721321 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14445983 33116 RMVar_ID_33116 Human_SNP_ID_701401213 A-to-I Human chr22 - 29502938 29502938 29502938 AAGATTTAAAAATTAGCCAGGCATGGTGGCGCATAATTGTAGTCCCAGCTACTCAGAAGGCAAAG AAGATTTAAAAATTAGCCAGGCATGGTGGCGCGTAATTGTAGTCCCAGCTACTCAGAAGGCAAAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1243398262 Functional Loss SNV dbSNP153 33..33 33 - - - 33117 RMVar_ID_33117 Human_SNP_ID_701401552 A-to-I Human chr22 - 29504415 29504415 29504415 GTGATCTGCCCGCTTCGGCCTCCCAAAGTGCTAGGATTACAGGCGTGAGCCACCGCGCCTGGCTA GTGATCTGCCCGCTTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCCTGGCTA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs767267223 Functional Loss SNV dbSNP153 33..33 33 - - - 33118 RMVar_ID_33118 Human_SNP_ID_701401747 A-to-I Human chr22 - 29504985 29504985 29504985 TGTGCGGCTAATTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTCAA TGTGCGGCTAATTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGGTCTCAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs949793939 Functional Loss SNV dbSNP153 33..33 33 - - - 33119 RMVar_ID_33119 Human_SNP_ID_701401954 A-to-I Human chr22 - 29505988 29505988 29505988 GGGCATGGTGGTGCGCGCCTGTAATCCCAGCCACTCGGGAGGCTGAGGCAGGAGAATTGCTTGAA GGGCATGGTGGTGCGCGCCTGTAATCCCAGCCGCTCGGGAGGCTGAGGCAGGAGAATTGCTTGAA T C THOC5 Ensembl:ENSG00000100296 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1339588592 Functional Loss SNV dbSNP153 33..33 33 - - - 33120 RMVar_ID_33120 Human_SNP_ID_701401974 A-to-I Human chr22 - 29506097 29506058 29506097 TATCAGTACTTTGGGAGGCTGGTGGGCGGATCACCTGAGATCAGGAGTTCAAGACCAGCCTGGCC TATCAGTACTTTGGGAGGCTGGTGGGCGGATC_________________________________ CCATGTTGGCCAGGCTGGTCTTGAACTCCTGATCTCAGGT C THOC5 Ensembl:ENSG00000100296 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1238341873 Functional Loss DEL dbSNP153 33..65 33 - - - Human_RBP_ID_7073011 33121 RMVar_ID_33121 Human_SNP_ID_701402000 A-to-I Human chr22 - 29506147 29506146 29506147 CTTCATTTTAAAAAATAAGATGGGCTGGGCACAGTGGCTTACGCCTTTAATATCAGTACTTTGGG CTTCATTTTAAAAAATAAGATGGGCTGGGCAC_GTGGCTTACGCCTTTAATATCAGTACTTTGGG CT C THOC5 Ensembl:ENSG00000100296 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1414165832 Functional Loss DEL dbSNP153 33..33 33 - - - 33122 RMVar_ID_33122 Human_SNP_ID_701402058 A-to-I Human chr22 - 29506422 29506422 29506422 ATGATCCTCCCACCTCGGCCTCCCAAAGTGCTAGGATTATAGGCATGAGCCACCACACCCGGCCT ATGATCCTCCCACCTCGGCCTCCCAAAGTGCTGGGATTATAGGCATGAGCCACCACACCCGGCCT T C THOC5 Ensembl:ENSG00000100296 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992103105 Functional Loss SNV dbSNP153 33..33 33 - - - 33123 RMVar_ID_33123 Human_SNP_ID_701402100 A-to-I Human chr22 - 29506561 29506561 29506561 TCAAGTGATCCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACCACAGGTGTGTGCCACCATTTCTG TCAAGTGATCCTCCTGCCTCAGCCTCCCAAGTGGCTGGGACCACAGGTGTGTGCCACCATTTCTG T C THOC5 Ensembl:ENSG00000100296 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs373051 Functional Loss SNV dbSNP153 33..33 33 - - - 33124 RMVar_ID_33124 Human_SNP_ID_701402110 A-to-I Human chr22 - 29506590 29506590 29506590 GCTCACTGCCGCCTCAACCTCTCCTGGGTTCAAGTGATCCTCCTGCCTCAGCCTCCCAAGTAGCT GCTCACTGCCGCCTCAACCTCTCCTGGGTTCAGGTGATCCTCCTGCCTCAGCCTCCCAAGTAGCT T C THOC5 Ensembl:ENSG00000100296 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909122676 Functional Loss SNV dbSNP153 33..33 33 - - - 33125 RMVar_ID_33125 Human_SNP_ID_701402132 A-to-I Human chr22 - 29506669 29506669 29506669 ATTTGAGGAGAATATTTTTTTTTTATTGAGACAGGGTCTTGCTCTGTTGTCCAGGCTGGAGTGCA ATTTGAGGAGAATATTTTTTTTTTATTGAGACGGGGTCTTGCTCTGTTGTCCAGGCTGGAGTGCA T C THOC5 Ensembl:ENSG00000100296 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs150540332 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14446140,Human_RBP_ID_26497455 33126 RMVar_ID_33126 Human_SNP_ID_701402134 A-to-I Human chr22 - 29506677 29506677 29506677 CAGGTAACATTTGAGGAGAATATTTTTTTTTTATTGAGACAGGGTCTTGCTCTGTTGTCCAGGCT CAGGTAACATTTGAGGAGAATATTTTTTTTTTGTTGAGACAGGGTCTTGCTCTGTTGTCCAGGCT T C THOC5 Ensembl:ENSG00000100296 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1011742230 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4691428,Human_RBP_ID_7073013,Human_RBP_ID_14446140,Human_RBP_ID_25663686,Human_RBP_ID_26497455 33127 RMVar_ID_33127 Human_SNP_ID_701402135 A-to-I Human chr22 - 29506677 29506677 29506677 CAGGTAACATTTGAGGAGAATATTTTTTTTTTATTGAGACAGGGTCTTGCTCTGTTGTCCAGGCT CAGGTAACATTTGAGGAGAATATTTTTTTTTTCTTGAGACAGGGTCTTGCTCTGTTGTCCAGGCT T G THOC5 Ensembl:ENSG00000100296 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1011742230 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4691428,Human_RBP_ID_7073013,Human_RBP_ID_14446140,Human_RBP_ID_25663686,Human_RBP_ID_26497455 33128 RMVar_ID_33128 Human_SNP_ID_701402215 A-to-I Human chr22 - 29507017 29507017 29507017 AAAAAATTTAAAAATCAGCCAGGTGTGGTGGTATGCACCAATAGTCCCAGTTACTCAGAAGGCTG AAAAAATTTAAAAATCAGCCAGGTGTGGTGGTGTGCACCAATAGTCCCAGTTACTCAGAAGGCTG T C THOC5 Ensembl:ENSG00000100296 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956045746 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26500104 33129 RMVar_ID_33129 Human_SNP_ID_701402231 A-to-I Human chr22 - 29507090 29507090 29507090 AAGGCGGGAGGATCCCTTGAGGCCAGGAGTTCAGGTCCAGCCTGGGCAACGTAGTGAGAGACCCT AAGGCGGGAGGATCCCTTGAGGCCAGGAGTTCCGGTCCAGCCTGGGCAACGTAGTGAGAGACCCT T G THOC5 Ensembl:ENSG00000100296 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1293937614 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25663687,Human_RBP_ID_26500105 33130 RMVar_ID_33130 Human_SNP_ID_701402240 A-to-I Human chr22 - 29507126 29507126 29507126 GGACTCATGACTGTAATCCTAGTACTTTGGAAAGCTAAGGCGGGAGGATCCCTTGAGGCCAGGAG GGACTCATGACTGTAATCCTAGTACTTTGGAAGGCTAAGGCGGGAGGATCCCTTGAGGCCAGGAG T C THOC5 Ensembl:ENSG00000100296 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1267602666 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8207889,Human_RBP_ID_26497458 33131 RMVar_ID_33131 Human_SNP_ID_701402330 A-to-I Human chr22 - 29507518 29507518 29507518 CCTGTCTCTACTAAAAACATGGAAATTAGCCAAGCGTGGTGGCGCATGCCTGTAGTCCCAGTTAC CCTGTCTCTACTAAAAACATGGAAATTAGCCAGGCGTGGTGGCGCATGCCTGTAGTCCCAGTTAC T C THOC5 Ensembl:ENSG00000100296 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs750897283 Functional Loss SNV dbSNP153 33..33 33 - - - 33132 RMVar_ID_33132 Human_SNP_ID_701409311 A-to-I Human chr22 - 29535808 29535808 29535808 GGGCATGGTGGCCTGTGCCTGTCGTCCCAGCTACTTGGAAGGCTGAGGCAGGAGGATCGCTCCAG GGGCATGGTGGCCTGTGCCTGTCGTCCCAGCTGCTTGGAAGGCTGAGGCAGGAGGATCGCTCCAG T C THOC5 Ensembl:ENSG00000100296 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1345162771 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119038,RMVar_hsa_circ_360960,RMVar_hsa_circ_213643,RMVar_hsa_circ_48679,RMVar_hsa_circ_1159,RMVar_hsa_circ_125251,RMVar_hsa_circ_23285,RMVar_hsa_circ_213648 33133 RMVar_ID_33133 Human_SNP_ID_701415630 A-to-I Human chr22 - 29559284 29559284 29559284 CACCAGCCTCGGCCTCCCAAAGTGCTGGGATTATAGGCATGAGCCACCGCACCTAGCCGGAAGTG CACCAGCCTCGGCCTCCCAAAGTGCTGGGATTGTAGGCATGAGCCACCGCACCTAGCCGGAAGTG T C NIPSNAP1 Ensembl:ENSG00000184117 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1332654849 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_213652,RMVar_hsa_circ_80436,RMVar_hsa_circ_122749,RMVar_hsa_circ_213653,RMVar_hsa_circ_63046,RMVar_hsa_circ_72109,RMVar_hsa_circ_338107 33134 RMVar_ID_33134 Human_SNP_ID_701417625 A-to-I Human chr22 - 29567927 29567927 29567927 ATGATCCTACCTCCTCGGCCTCCCAAAGTGCTAGGATTGTAGACATGAGCCACCGTGCCTGGCCT ATGATCCTACCTCCTCGGCCTCCCAAAGTGCTGGGATTGTAGACATGAGCCACCGTGCCTGGCCT T C NIPSNAP1 Ensembl:ENSG00000184117 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947271949 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14447018 RMVar_hsa_circ_63046,RMVar_hsa_circ_338107,RMVar_hsa_circ_69306 33135 RMVar_ID_33135 Human_SNP_ID_701428669 A-to-I Human chr22 + 29608093 29608093 29608093 TACGCGGGAGGCTGAGGCAGGAGAATTCCTTGAACCTGGGAGGCGGAGGTTGCAGTGAGCCAAGA TACGCGGGAGGCTGAGGCAGGAGAATTCCTTGTACCTGGGAGGCGGAGGTTGCAGTGAGCCAAGA A T NF2 Ensembl:ENSG00000186575 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1171019939 Functional Loss SNV dbSNP153 33..33 33 - - - 33136 RMVar_ID_33136 Human_SNP_ID_701447493 A-to-I Human chr22 + 29689205 29689201 29689205 GTCTCAAAAAAAAAAAAAAAAAAAAAAAGAGAAAGTAAAGAAAAGCTTGATCTGGCCACTTAGTA GTCTCAAAAAAAAAAAAAAAAAAAAAAAG____AGTAAAGAAAAGCTTGATCTGGCCACTTAGTA GAGAA G NF2 Ensembl:ENSG00000186575 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs975398230 Functional Loss DEL dbSNP153 30..33 33 - - - 33137 RMVar_ID_33137 Human_SNP_ID_701447498 A-to-I Human chr22 + 29689205 29689205 29689205 GTCTCAAAAAAAAAAAAAAAAAAAAAAAGAGAAAGTAAAGAAAAGCTTGATCTGGCCACTTAGTA GTCTCAAAAAAAAAAAAAAAAAAAAAAAGAGAGAGTAAAGAAAAGCTTGATCTGGCCACTTAGTA A G NF2 Ensembl:ENSG00000186575 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs897312714 Functional Loss SNV dbSNP153 33..33 33 - - - 33138 RMVar_ID_33138 Human_SNP_ID_701467626 A-to-I Human chr22 + 29768726 29768726 29768726 ACAGCTCACTGCAGCCTTGACCTCCTGGGTTCAAGTGATCTTCCCACCTCAGCCTCCTGAGTAGC ACAGCTCACTGCAGCCTTGACCTCCTGGGTTCGAGTGATCTTCCCACCTCAGCCTCCTGAGTAGC A G UQCR10 Ensembl:ENSG00000184076 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1406890548 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94407,RMVar_hsa_circ_213673 33139 RMVar_ID_33139 Human_SNP_ID_701481157 A-to-I Human chr22 - 29824432 29824432 29824432 TATTTGATTTTTAGTAGAGACGAGGTCTCGCTATGTTTCTCAGGCTAGTCTTGAACTCCTGAACT TATTTGATTTTTAGTAGAGACGAGGTCTCGCTGTGTTTCTCAGGCTAGTCTTGAACTCCTGAACT T C ASCC2 Ensembl:ENSG00000100325 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs548514464 Functional Loss SNV dbSNP153 33..33 33 - - - 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_41965,RMVar_hsa_circ_299386,RMVar_hsa_circ_213684,RMVar_hsa_circ_343798,RMVar_hsa_circ_351518,RMVar_hsa_circ_377201,RMVar_hsa_circ_98815,RMVar_hsa_circ_49828,RMVar_hsa_circ_213685,RMVar_hsa_circ_213687,RMVar_hsa_circ_213686,RMVar_hsa_circ_75235,RMVar_hsa_circ_213691,RMVar_hsa_circ_123113,RMVar_hsa_circ_311739,RMVar_hsa_circ_270126,RMVar_hsa_circ_213692,RMVar_hsa_circ_302936,RMVar_hsa_circ_213694,RMVar_hsa_circ_213695 33140 RMVar_ID_33140 Human_SNP_ID_701481700 A-to-I Human chr22 - 29826385 29826385 29826385 CTAAGCCCAGGAGGTAGAGGCTGCCGTGAGCCAAGATTATGCCACTCCACTTCAGCCTGGGCAAC CTAAGCCCAGGAGGTAGAGGCTGCCGTGAGCCCAGATTATGCCACTCCACTTCAGCCTGGGCAAC T G ASCC2 Ensembl:ENSG00000100325 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1421631997 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117793,RMVar_hsa_circ_126221,RMVar_hsa_circ_213676,RMVar_hsa_circ_213677,RMVar_hsa_circ_109203,RMVar_hsa_circ_1091,RMVar_hsa_circ_213682,RMVar_hsa_circ_41965,RMVar_hsa_circ_213684,RMVar_hsa_circ_343798,RMVar_hsa_circ_351518,RMVar_hsa_circ_98815,RMVar_hsa_circ_49828,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 33141 RMVar_ID_33141 Human_SNP_ID_701482556 A-to-I Human chr22 - 29829538 29829538 29829538 TTTTGTGTTTTTAGCAGAGACGGGGTTTCACCATGTTGGCCAGGCTAGTCTCGAACTCCTGACCT TTTTGTGTTTTTAGCAGAGACGGGGTTTCACCGTGTTGGCCAGGCTAGTCTCGAACTCCTGACCT T C ASCC2 Ensembl:ENSG00000100325 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs918283158 Functional Loss SNV dbSNP153 33..33 33 - - - 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 33142 RMVar_ID_33142 Human_SNP_ID_701483849 A-to-I Human chr22 - 29835175 29835175 29835175 TTAGGCTGGTCTCAAACTCCTGGCTTCGAGCAATCCTCCTGCCTTGGCTTCCCAAGTGCTGGGAT TTAGGCTGGTCTCAAACTCCTGGCTTCGAGCAGTCCTCCTGCCTTGGCTTCCCAAGTGCTGGGAT T C ASCC2 Ensembl:ENSG00000100325 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978715231 Functional Loss SNV dbSNP153 33..33 33 - - - 33143 RMVar_ID_33143 Human_SNP_ID_701484208 A-to-I Human chr22 - 29836596 29836596 29836596 AGATCGTTCCTCTGCACTCTAGCCTGGGTGACAGAGTGAGACTCCATCTCAAAAAAAAAGGAATG AGATCGTTCCTCTGCACTCTAGCCTGGGTGACTGAGTGAGACTCCATCTCAAAAAAAAAGGAATG T A ASCC2 Ensembl:ENSG00000100325 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs553952825 Functional Loss SNV dbSNP153 33..33 33 - - - 33144 RMVar_ID_33144 Human_SNP_ID_701484209 A-to-I Human chr22 - 29836596 29836596 29836596 AGATCGTTCCTCTGCACTCTAGCCTGGGTGACAGAGTGAGACTCCATCTCAAAAAAAAAGGAATG AGATCGTTCCTCTGCACTCTAGCCTGGGTGACGGAGTGAGACTCCATCTCAAAAAAAAAGGAATG T C ASCC2 Ensembl:ENSG00000100325 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs553952825 Functional Loss SNV dbSNP153 33..33 33 - - - 33145 RMVar_ID_33145 Human_SNP_ID_701484230 A-to-I Human chr22 - 29836672 29836672 29836672 CCTGTATTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCTCTTGAACCCGGGAGACAGAGGTG CCTGTATTCCCAGCTACTCGGGAGGCTGAGGCGGGAGAATCTCTTGAACCCGGGAGACAGAGGTG T C ASCC2 Ensembl:ENSG00000100325 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs765892468 Functional Loss SNV dbSNP153 33..33 33 - - - 33146 RMVar_ID_33146 Human_SNP_ID_701497434 A-to-I Human chr22 + 29890006 29890006 29890006 TAGGCTCACTGCAGCCTCTGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGC TAGGCTCACTGCAGCCTCTGCCTCCCGGGTTCGAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGC A G MTMR3 Ensembl:ENSG00000100330 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1359902759 Functional Loss SNV dbSNP153 33..33 33 - - - 33147 RMVar_ID_33147 Human_SNP_ID_701497531 A-to-I Human chr22 + 29890363 29890363 29890363 ACATGGTAAAACCCCGTCTCTACTAAAAATACAAAAATCAGTCGGGTGTGGTGGCGGGCCTCTGT ACATGGTAAAACCCCGTCTCTACTAAAAATACGAAAATCAGTCGGGTGTGGTGGCGGGCCTCTGT A G MTMR3 Ensembl:ENSG00000100330 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1040853490 Functional Loss SNV dbSNP153 33..33 33 - - - 33148 RMVar_ID_33148 Human_SNP_ID_701497545 A-to-I Human chr22 + 29890443 29890443 29890443 GAAGGCTGAGGCACAGAGAATCACTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCCGAGATTAAG GAAGGCTGAGGCACAGAGAATCACTTGAACCCCGGAGGCAGAGGTTGCAGTGAGCCGAGATTAAG A C MTMR3 Ensembl:ENSG00000100330 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs959904984 Functional Loss SNV dbSNP153 33..33 33 - - - 33149 RMVar_ID_33149 Human_SNP_ID_701499282 A-to-I Human chr22 + 29897465 29897465 29897465 AAGTATGTTTTTATTTATTTATTTATTTATTTATTTTTGAGACGGGCTCTCACTCTGTTGCCCAT AAGTATGTTTTTATTTATTTATTTATTTATTTGTTTTTGAGACGGGCTCTCACTCTGTTGCCCAT A G MTMR3 Ensembl:ENSG00000100330 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1376718968 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7073708,Human_RBP_ID_14450169 33150 RMVar_ID_33150 Human_SNP_ID_701500576 A-to-I Human chr22 + 29903414 29903414 29903414 TTTTCTTTCTTTTTTTTTTTTTTTTTTGAGACAGGGTCTTACTGTCATCCAGGCTGGAGTGCAGT TTTTCTTTCTTTTTTTTTTTTTTTTTTGAGACTGGGTCTTACTGTCATCCAGGCTGGAGTGCAGT A T MTMR3 Ensembl:ENSG00000100330 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1227028094 Functional Loss SNV dbSNP153 33..33 33 - - - 33151 RMVar_ID_33151 Human_SNP_ID_701519651 A-to-I Human chr22 + 29975789 29975789 29975789 CACTGTGCCCATCTAGTTTCTCTATTTTTTGTAGAGATGGTGTCTCACCATGTTGCCCAGGCTGG CACTGTGCCCATCTAGTTTCTCTATTTTTTGTGGAGATGGTGTCTCACCATGTTGCCCAGGCTGG A G MTMR3 Ensembl:ENSG00000100330 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs896179167 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_213699,RMVar_hsa_circ_109118,RMVar_hsa_circ_336037,RMVar_hsa_circ_349606,RMVar_hsa_circ_286805,RMVar_hsa_circ_213702,RMVar_hsa_circ_316921,RMVar_hsa_circ_366895,RMVar_hsa_circ_213698,RMVar_hsa_circ_367363,RMVar_hsa_circ_334273,RMVar_hsa_circ_273774,RMVar_hsa_circ_300288,RMVar_hsa_circ_270938,RMVar_hsa_circ_213704,RMVar_hsa_circ_213706,RMVar_hsa_circ_101519,RMVar_hsa_circ_213705,RMVar_hsa_circ_213703 33152 RMVar_ID_33152 Human_SNP_ID_701610342 A-to-I Human chr22 - 30355121 30355121 30355121 TAATCCCCACTATTCGGGAGAGAATTGCTTGAACCTGGGAAGCAGAAGTTGCAATGAGCCAAGAT TAATCCCCACTATTCGGGAGAGAATTGCTTGAGCCTGGGAAGCAGAAGTTGCAATGAGCCAAGAT T C SF3A1 Ensembl:ENSG00000099995 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1461145512 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106607,RMVar_hsa_circ_213740 33153 RMVar_ID_33153 Human_SNP_ID_701618971 A-to-I Human chr22 - 30385738 30385738 30385738 TCGTGTTGCCCAGGCTGGAGTGCAGTGGCGCAATCTCGGCTCACTGGAACCTCTGCCTTCCAGGT TCGTGTTGCCCAGGCTGGAGTGCAGTGGCGCAGTCTCGGCTCACTGGAACCTCTGCCTTCCAGGT T C RNF215 Ensembl:ENSG00000099999 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs746672114 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27035217 33154 RMVar_ID_33154 Human_SNP_ID_701626393 A-to-I Human chr22 - 30413912 30413912 30413912 ATCATTTGAGCCCAGGAGATTGAGGCTCCAGTAAGCCGTGATCACGCCACTGTACTCCAGCCTGA ATCATTTGAGCCCAGGAGATTGAGGCTCCAGTGAGCCGTGATCACGCCACTGTACTCCAGCCTGA T C RNF215 Ensembl:ENSG00000099999 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1138069 Functional Loss SNV dbSNP153 33..33 33 - - - 33155 RMVar_ID_33155 Human_SNP_ID_701626428 A-to-I Human chr22 + 30414092 30414092 30414092 GGATCAAGCAATCCTCCTGCCTCAGCCTCCCAAATCACTGGGATTACAGGCATGAGCCACTGCAC GGATCAAGCAATCCTCCTGCCTCAGCCTCCCACATCACTGGGATTACAGGCATGAGCCACTGCAC A C AC004832.3,SEC14L2 Ensembl:ENSG00000249590,Ensembl:ENSG00000100003 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs571431304 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_358938 33156 RMVar_ID_33156 Human_SNP_ID_701645029 A-to-I Human chr22 - 30487528 30487528 30487528 TCTGGAGGCGGAGCTTGCAGTGAGGCGAGATCACGCCACTGCACTCCAGCCTGGGCGACAGAGCG TCTGGAGGCGGAGCTTGCAGTGAGGCGAGATCGCGCCACTGCACTCCAGCCTGGGCGACAGAGCG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs530205760 Functional Loss SNV dbSNP153 33..33 33 - - - 33157 RMVar_ID_33157 Human_SNP_ID_701645030 A-to-I Human chr22 - 30487528 30487528 30487528 TCTGGAGGCGGAGCTTGCAGTGAGGCGAGATCACGCCACTGCACTCCAGCCTGGGCGACAGAGCG TCTGGAGGCGGAGCTTGCAGTGAGGCGAGATCCCGCCACTGCACTCCAGCCTGGGCGACAGAGCG T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs530205760 Functional Loss SNV dbSNP153 33..33 33 - - - 33158 RMVar_ID_33158 Human_SNP_ID_701645037 A-to-I Human chr22 - 30487542 30487542 30487542 GAGAATGACGTGAATCTGGAGGCGGAGCTTGCAGTGAGGCGAGATCACGCCACTGCACTCCAGCC GAGAATGACGTGAATCTGGAGGCGGAGCTTGCGGTGAGGCGAGATCACGCCACTGCACTCCAGCC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs538875722 Functional Loss SNV dbSNP153 33..33 33 - - - 33159 RMVar_ID_33159 Human_SNP_ID_701645038 A-to-I Human chr22 - 30487542 30487542 30487542 GAGAATGACGTGAATCTGGAGGCGGAGCTTGCAGTGAGGCGAGATCACGCCACTGCACTCCAGCC GAGAATGACGTGAATCTGGAGGCGGAGCTTGCCGTGAGGCGAGATCACGCCACTGCACTCCAGCC T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs538875722 Functional Loss SNV dbSNP153 33..33 33 - - - 33160 RMVar_ID_33160 Human_SNP_ID_701645159 A-to-I Human chr22 - 30487964 30487964 30487964 AAACCCCTGACCTCAAGTGATCTGCCTGGCTCAGCCTCCCAAAGTGCTGGGATTACAGGTATGAG AAACCCCTGACCTCAAGTGATCTGCCTGGCTCGGCCTCCCAAAGTGCTGGGATTACAGGTATGAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1262475554 Functional Loss SNV dbSNP153 33..33 33 - - - 33161 RMVar_ID_33161 Human_SNP_ID_701645190 A-to-I Human chr22 - 30488139 30488137 30488140 ACTGGAGTACAGTGGCGCGATCTCAGCTCACTACAACATTCACCTCCCAGGTTCAAGCGATTCTC ACTGGAGTACAGTGGCGCGATCTCAGCTCAC___AACATTCACCTCCCAGGTTCAAGCGATTCTC TGTA T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1569237947 Functional Loss DEL dbSNP153 32..34 33 - - - 33162 RMVar_ID_33162 Human_SNP_ID_701645191 A-to-I Human chr22 - 30488139 30488139 30488139 ACTGGAGTACAGTGGCGCGATCTCAGCTCACTACAACATTCACCTCCCAGGTTCAAGCGATTCTC ACTGGAGTACAGTGGCGCGATCTCAGCTCACTGCAACATTCACCTCCCAGGTTCAAGCGATTCTC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs533921325 Functional Loss SNV dbSNP153 33..33 33 - - - 33163 RMVar_ID_33163 Human_SNP_ID_701692759 A-to-I Human chr22 + 30647299 30647299 30647299 GCGTGCCTATAGTCCCAGCTACATGGGAGGCTAAGGTGGGAGGATCACTTGAGCCCTGGAGATCG GCGTGCCTATAGTCCCAGCTACATGGGAGGCTCAGGTGGGAGGATCACTTGAGCCCTGGAGATCG A C SLC35E4 Ensembl:ENSG00000100036 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1461994894 Functional Loss SNV dbSNP153 33..33 33 - - - 33164 RMVar_ID_33164 Human_SNP_ID_701696173 A-to-I Human chr22 - 30659645 30659645 30659645 TTTCTTAGTTCTAAAATTCTTATTTAGCCTGTAATCCCTGCACTTTGGGAGGTTGAGGCTGGTGG TTTCTTAGTTCTAAAATTCTTATTTAGCCTGTTATCCCTGCACTTTGGGAGGTTGAGGCTGGTGG T A DUSP18 Ensembl:ENSG00000167065 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1398573176 Functional Loss SNV dbSNP153 33..33 33 - - - 33165 RMVar_ID_33165 Human_SNP_ID_701696336 A-to-I Human chr22 - 30660337 30660336 30660338 ATCGTGCCTCTGCTCTCCAGCCTGAGTGACAAAGTGAGACTGTGTTTCAAAAAAAAAATTTTTTT ATCGTGCCTCTGCTCTCCAGCCTGAGTGACA__GTGAGACTGTGTTTCAAAAAAAAAATTTTTTT CTT C DUSP18 Ensembl:ENSG00000167065 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1310129643 Functional Loss DEL dbSNP153 32..33 33 - - - 33166 RMVar_ID_33166 Human_SNP_ID_701696336 A-to-I Human chr22 - 30660338 30660336 30660338 GATCGTGCCTCTGCTCTCCAGCCTGAGTGACAAAGTGAGACTGTGTTTCAAAAAAAAAATTTTTT GATCGTGCCTCTGCTCTCCAGCCTGAGTGACA__GTGAGACTGTGTTTCAAAAAAAAAATTTTTT CTT C DUSP18 Ensembl:ENSG00000167065 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1310129643 Functional Loss DEL dbSNP153 33..34 33 - - - 33167 RMVar_ID_33167 Human_SNP_ID_701732017 A-to-I Human chr22 + 30808232 30808232 30808232 CCCCCCAAAAGATATGTTAGGCCGGGCATGGTAGCTCACACCTATATTCCCAGCACTTTGGGAGG CCCCCCAAAAGATATGTTAGGCCGGGCATGGTCGCTCACACCTATATTCCCAGCACTTTGGGAGG A C OSBP2 Ensembl:ENSG00000184792 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1440294147 Functional Loss SNV dbSNP153 33..33 33 - - - 33168 RMVar_ID_33168 Human_SNP_ID_701755570 A-to-I Human chr22 + 30905402 30905402 30905402 CTGACCTCGTGATCCACCGGCCTCAGCCTCCCAAAGCGCTGGGATTACAGGCGTGAGCCACCGTG CTGACCTCGTGATCCACCGGCCTCAGCCTCCCGAAGCGCTGGGATTACAGGCGTGAGCCACCGTG A G OSBP2 Ensembl:ENSG00000184792 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1044451187 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48897,RMVar_hsa_circ_213764 33169 RMVar_ID_33169 Human_SNP_ID_701759841 A-to-I Human chr22 - 30922797 30922797 30922797 GAACTCCCAGTCTCGAGAGATCCATCTGCCTCAGCCTCCCAAAGGGCTGGGATTACAGACGTGAG GAACTCCCAGTCTCGAGAGATCCATCTGCCTCTGCCTCCCAAAGGGCTGGGATTACAGACGTGAG T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335088212 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14454535 33170 RMVar_ID_33170 Human_SNP_ID_701769612 A-to-I Human chr22 - 30962111 30962111 30962111 TGCATGCAACCTCTACCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCTCAAGTAGTTAGGA TGCATGCAACCTCTACCTCCCGGGTTCAAGCGGTTCTCCTGCCTCAGCCTCTCAAGTAGTTAGGA T C MORC2 Ensembl:ENSG00000133422 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1303171508 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_65272,RMVar_hsa_circ_48694,RMVar_hsa_circ_335141 33171 RMVar_ID_33171 Human_SNP_ID_701769614 A-to-I Human chr22 - 30962115 30962115 30962115 TCACTGCATGCAACCTCTACCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCTCAAGTAGTT TCACTGCATGCAACCTCTACCTCCCGGGTTCACGCGATTCTCCTGCCTCAGCCTCTCAAGTAGTT T G MORC2 Ensembl:ENSG00000133422 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs953441609 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_65272,RMVar_hsa_circ_48694,RMVar_hsa_circ_335141 33172 RMVar_ID_33172 Human_SNP_ID_701769917 A-to-I Human chr22 - 30963156 30963156 30963156 CTGGTTAACATGGTGAAACCCCGTCTGTACTAAAAATACAAAAAAATTATCTGGGCGTGGCTGCG CTGGTTAACATGGTGAAACCCCGTCTGTACTAGAAATACAAAAAAATTATCTGGGCGTGGCTGCG T C MORC2 Ensembl:ENSG00000133422 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1183272034 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_65272,RMVar_hsa_circ_48694,RMVar_hsa_circ_335141 33173 RMVar_ID_33173 Human_SNP_ID_701770712 A-to-I Human chr22 - 30966702 30966702 30966702 GCAATCTTGGCTCACTGCAACCTTCACCTCCCAGGTTCAAACGATTCTCCTGCCTCAGCTTCCCA GCAATCTTGGCTCACTGCAACCTTCACCTCCCGGGTTCAAACGATTCTCCTGCCTCAGCTTCCCA T C MORC2 Ensembl:ENSG00000133422 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1013784547 Functional Loss SNV dbSNP153 33..33 33 - - - 33174 RMVar_ID_33174 Human_SNP_ID_701770727 A-to-I Human chr22 - 30966747 30966747 30966747 GAGAGACGGAGTCTTGCTCTGTTGCTCAGGCTAGAGTGGGGTGGCGCAATCTTGGCTCACTGCAA GAGAGACGGAGTCTTGCTCTGTTGCTCAGGCTTGAGTGGGGTGGCGCAATCTTGGCTCACTGCAA T A MORC2 Ensembl:ENSG00000133422 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1219591199 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2716331,Human_RBP_ID_14455523,Human_RBP_ID_27035330 33175 RMVar_ID_33175 Human_SNP_ID_701830640 A-to-I Human chr22 + 31198833 31198833 31198833 ATTAAGGTTCTCGGCTGGGCGTGGTGGCTCACACCTGTAATCTCAGCACTTTGGGAGGCTGAGGC ATTAAGGTTCTCGGCTGGGCGTGGTGGCTCACGCCTGTAATCTCAGCACTTTGGGAGGCTGAGGC A G RNF185 Ensembl:ENSG00000138942 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs530255160 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_338987,RMVar_hsa_circ_213788,RMVar_hsa_circ_84473 33176 RMVar_ID_33176 Human_SNP_ID_701837100 A-to-I Human chr22 + 31226633 31226632 31226634 ATTATTATTATTATTGTTATTATTATTGAGACAGAGTCTCGCTCTGTCGCCCAGGCTGGTGTACA ATTATTATTATTATTGTTATTATTATTGAGAC__AGTCTCGCTCTGTCGCCCAGGCTGGTGTACA CAG C LIMK2 Ensembl:ENSG00000182541 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1247431106 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_50381,RMVar_hsa_circ_213789,RMVar_hsa_circ_94950,RMVar_hsa_circ_350119 33177 RMVar_ID_33177 Human_SNP_ID_701837102 A-to-I Human chr22 + 31226635 31226635 31226635 TATTATTATTATTGTTATTATTATTGAGACAGAGTCTCGCTCTGTCGCCCAGGCTGGTGTACAGT TATTATTATTATTGTTATTATTATTGAGACAGTGTCTCGCTCTGTCGCCCAGGCTGGTGTACAGT A T LIMK2 Ensembl:ENSG00000182541 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1356789422 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50381,RMVar_hsa_circ_213789,RMVar_hsa_circ_94950,RMVar_hsa_circ_350119 33178 RMVar_ID_33178 Human_SNP_ID_701838776 A-to-I Human chr22 + 31234112 31234112 31234112 TCGGCTCACTGCAACTTCTGCCTCCCGGGTTTAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGC TCGGCTCACTGCAACTTCTGCCTCCCGGGTTTGAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGC A G LIMK2 Ensembl:ENSG00000182541 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs745537972 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50381,RMVar_hsa_circ_213789,RMVar_hsa_circ_94950,RMVar_hsa_circ_350119 33179 RMVar_ID_33179 Human_SNP_ID_701839339 A-to-I Human chr22 + 31236454 31236454 31236454 AACAGAGCAAGACCTCATCCCCACAAAAAATCAAAAATTTAGCCAGGCATGGTGGCTCATGCCTG AACAGAGCAAGACCTCATCCCCACAAAAAATCGAAAATTTAGCCAGGCATGGTGGCTCATGCCTG A G LIMK2 Ensembl:ENSG00000182541 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1478609848 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50381,RMVar_hsa_circ_213789,RMVar_hsa_circ_94950,RMVar_hsa_circ_350119 33180 RMVar_ID_33180 Human_SNP_ID_701851527 A-to-I Human chr22 - 31284101 31284090 31284101 TCGGGAGTTCGAGACCAGCCTGACCACCATGGAGAAACCCCATCTCTACTAAAAATACAAAATAC TCGGGAGTTCGAGACCAGCCTGACCACCATGG___________CTCTACTAAAAATACAAAATAC GATGGGGTTTCT G PIK3IP1 Ensembl:ENSG00000100100 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1569010286 Functional Loss DEL dbSNP153 33..43 33 - - - 33181 RMVar_ID_33181 Human_SNP_ID_701851535 A-to-I Human chr22 - 31284098 31284098 31284098 GGAGTTCGAGACCAGCCTGACCACCATGGAGAAACCCCATCTCTACTAAAAATACAAAATACTCT GGAGTTCGAGACCAGCCTGACCACCATGGAGAGACCCCATCTCTACTAAAAATACAAAATACTCT T C PIK3IP1 Ensembl:ENSG00000100100 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1255816340 Functional Loss SNV dbSNP153 33..33 33 - - - 33182 RMVar_ID_33182 Human_SNP_ID_701861371 A-to-I Human chr22 + 31323523 31323523 31323523 GGAGGTGAGCCGAGATAGCACCACTGCAGCCTAGGTGACAGAGTGAGACTCTGTCTAAAAAAAAA GGAGGTGAGCCGAGATAGCACCACTGCAGCCTGGGTGACAGAGTGAGACTCTGTCTAAAAAAAAA A G PIK3IP1-AS1 Ensembl:ENSG00000228839 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1439400043 Functional Loss SNV dbSNP153 33..33 33 - - - 33183 RMVar_ID_33183 Human_SNP_ID_701868363 A-to-I Human chr22 + 31349659 31349659 31349659 TTGGCTCACTGCAATCTCTACCTCCTGGGTTCAAGCGGTTCTCTTGCCTCAGTCTTCCAAGTAGC TTGGCTCACTGCAATCTCTACCTCCTGGGTTCCAGCGGTTCTCTTGCCTCAGTCTTCCAAGTAGC A C LINC01521 RNACentral:URS000075C3AE lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1183407772 Functional Loss SNV dbSNP153 33..33 33 - - - 33184 RMVar_ID_33184 Human_SNP_ID_701868392 A-to-I Human chr22 + 31349760 31349760 31349760 TGTTGTATTTTTAGTAGAGATGGGGTTTCGCCATGTTGGCCAGACTGGTCTCGAACTCCTGACCT TGTTGTATTTTTAGTAGAGATGGGGTTTCGCCGTGTTGGCCAGACTGGTCTCGAACTCCTGACCT A G LINC01521 RNACentral:URS000075C3AE lincRNA intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs947467135 Functional Loss SNV dbSNP153 33..33 33 - - - 33185 RMVar_ID_33185 Human_SNP_ID_701868415 A-to-I Human chr22 + 31349842 31349842 31349842 TCAGCCTCCCAAGGTGCTGGGATTACAGACGTAAGCCACCATGCCCAGCCTGGATATTTTATTTA TCAGCCTCCCAAGGTGCTGGGATTACAGACGTTAGCCACCATGCCCAGCCTGGATATTTTATTTA A T LINC01521 RNACentral:URS000075C3AE lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1329450677 Functional Loss SNV dbSNP153 33..33 33 - - - 33186 RMVar_ID_33186 Human_SNP_ID_701882775 A-to-I Human chr22 + 31406581 31406581 31406581 TCTTTAATACCAGCTCCTAGGGAGGTTGAGGCAGGAGAATTGCTTGAACCTGGGAGGCAGATGTT TCTTTAATACCAGCTCCTAGGGAGGTTGAGGCGGGAGAATTGCTTGAACCTGGGAGGCAGATGTT A G DRG1 Ensembl:ENSG00000185721 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs745952871 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113269,RMVar_hsa_circ_213802,RMVar_hsa_circ_120142,RMVar_hsa_circ_111920,RMVar_hsa_circ_350520,RMVar_hsa_circ_213803,RMVar_hsa_circ_370515,RMVar_hsa_circ_341891,RMVar_hsa_circ_335174,RMVar_hsa_circ_213806,RMVar_hsa_circ_213807,RMVar_hsa_circ_213805 33187 RMVar_ID_33187 Human_SNP_ID_701882977 A-to-I Human chr22 + 31407519 31407519 31407519 TACCATGCCTGACTAATTTTTTATTTTTTTGTAGAGACAGAGTCTCAATATGTTGTCCAGGCTGG TACCATGCCTGACTAATTTTTTATTTTTTTGTGGAGACAGAGTCTCAATATGTTGTCCAGGCTGG A G DRG1 Ensembl:ENSG00000185721 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs141325737 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2716527,Human_RBP_ID_14537733 RMVar_hsa_circ_113269,RMVar_hsa_circ_213802,RMVar_hsa_circ_120142,RMVar_hsa_circ_111920,RMVar_hsa_circ_350520,RMVar_hsa_circ_213803,RMVar_hsa_circ_370515,RMVar_hsa_circ_341891,RMVar_hsa_circ_335174,RMVar_hsa_circ_213806,RMVar_hsa_circ_213807,RMVar_hsa_circ_213805 33188 RMVar_ID_33188 Human_SNP_ID_701883077 A-to-I Human chr22 + 31407863 31407863 31407863 TATGTTTTGGTCAGGCGTGGTGGTTCAAGCCTATAATCCCAGCACTTTGGGAGGCCGAGGTGAGC TATGTTTTGGTCAGGCGTGGTGGTTCAAGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGAGC A G DRG1 Ensembl:ENSG00000185721 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs989717793 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113269,RMVar_hsa_circ_213802,RMVar_hsa_circ_120142,RMVar_hsa_circ_111920,RMVar_hsa_circ_350520,RMVar_hsa_circ_213803,RMVar_hsa_circ_370515,RMVar_hsa_circ_341891,RMVar_hsa_circ_335174,RMVar_hsa_circ_213806,RMVar_hsa_circ_213807,RMVar_hsa_circ_213805 33189 RMVar_ID_33189 Human_SNP_ID_701883107 A-to-I Human chr22 + 31407979 31407979 31407979 CCTGTCTCTACTAAAAATACACAAAAAAAATTAGTGGGGCATGGTGGCGGGCACCTGTAATCCCA CCTGTCTCTACTAAAAATACACAAAAAAAATTGGTGGGGCATGGTGGCGGGCACCTGTAATCCCA A G DRG1 Ensembl:ENSG00000185721 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs891353069 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113269,RMVar_hsa_circ_213802,RMVar_hsa_circ_120142,RMVar_hsa_circ_111920,RMVar_hsa_circ_350520,RMVar_hsa_circ_213803,RMVar_hsa_circ_370515,RMVar_hsa_circ_341891,RMVar_hsa_circ_335174,RMVar_hsa_circ_213806,RMVar_hsa_circ_213807,RMVar_hsa_circ_213805 33190 RMVar_ID_33190 Human_SNP_ID_701883264 A-to-I Human chr22 + 31408614 31408614 31408614 TACTAAAAATACATAAAAAAAATTGGTGGGGCATGGTGGCGAGCACCTGTAATCCCAGCTGCTCA TACTAAAAATACATAAAAAAAATTGGTGGGGCGTGGTGGCGAGCACCTGTAATCCCAGCTGCTCA A G DRG1 Ensembl:ENSG00000185721 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs560064483 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7075583 RMVar_hsa_circ_113269,RMVar_hsa_circ_213802,RMVar_hsa_circ_120142,RMVar_hsa_circ_111920,RMVar_hsa_circ_350520,RMVar_hsa_circ_213803,RMVar_hsa_circ_370515,RMVar_hsa_circ_341891,RMVar_hsa_circ_335174,RMVar_hsa_circ_213806,RMVar_hsa_circ_213807,RMVar_hsa_circ_213805 33191 RMVar_ID_33191 Human_SNP_ID_701883587 A-to-I Human chr22 + 31409847 31409847 31409847 GAAACCCTGACTCTACTAAAATACAAAAAATTAGTCAGATATGGTGGCATATGCCCTGTAGTCCC GAAACCCTGACTCTACTAAAATACAAAAAATTTGTCAGATATGGTGGCATATGCCCTGTAGTCCC A T DRG1 Ensembl:ENSG00000185721 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1379304551 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113269,RMVar_hsa_circ_213802,RMVar_hsa_circ_120142,RMVar_hsa_circ_111920,RMVar_hsa_circ_350520,RMVar_hsa_circ_213803,RMVar_hsa_circ_370515,RMVar_hsa_circ_341891,RMVar_hsa_circ_335174,RMVar_hsa_circ_213806,RMVar_hsa_circ_213807,RMVar_hsa_circ_213805 33192 RMVar_ID_33192 Human_SNP_ID_701885803 A-to-I Human chr22 + 31418399 31418393 31418400 ATGATCAGTTGAGCCCAGGAGGTGGAGGTTATAATGAGCTATGATCATGCGACTGCACTCCAGCC ATGATCAGTTGAGCCCAGGAGGTGGAG_______TGAGCTATGATCATGCGACTGCACTCCAGCC GGTTATAA G DRG1 Ensembl:ENSG00000185721 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1481613174 Functional Loss DEL dbSNP153 28..34 33 - - - RMVar_hsa_circ_113269,RMVar_hsa_circ_213802,RMVar_hsa_circ_120142,RMVar_hsa_circ_66148,RMVar_hsa_circ_111920,RMVar_hsa_circ_350520,RMVar_hsa_circ_213803,RMVar_hsa_circ_370515,RMVar_hsa_circ_341891,RMVar_hsa_circ_213806,RMVar_hsa_circ_213807,RMVar_hsa_circ_213805,RMVar_hsa_circ_340965,RMVar_hsa_circ_347968,RMVar_hsa_circ_75970,RMVar_hsa_circ_213808 33193 RMVar_ID_33193 Human_SNP_ID_701885805 A-to-I Human chr22 + 31418399 31418399 31418399 ATGATCAGTTGAGCCCAGGAGGTGGAGGTTATAATGAGCTATGATCATGCGACTGCACTCCAGCC ATGATCAGTTGAGCCCAGGAGGTGGAGGTTATCATGAGCTATGATCATGCGACTGCACTCCAGCC A C DRG1 Ensembl:ENSG00000185721 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1378442662 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113269,RMVar_hsa_circ_213802,RMVar_hsa_circ_120142,RMVar_hsa_circ_66148,RMVar_hsa_circ_111920,RMVar_hsa_circ_350520,RMVar_hsa_circ_213803,RMVar_hsa_circ_370515,RMVar_hsa_circ_341891,RMVar_hsa_circ_213806,RMVar_hsa_circ_213807,RMVar_hsa_circ_213805,RMVar_hsa_circ_340965,RMVar_hsa_circ_347968,RMVar_hsa_circ_75970,RMVar_hsa_circ_213808 33194 RMVar_ID_33194 Human_SNP_ID_701889339 A-to-I Human chr22 + 31431109 31431109 31431109 CCAGGCTGAGTGCAGTGGTGCGATCTCGGCTCACTGCAAGCTCCGCCTCCCGGGTTCATGCCATT CCAGGCTGAGTGCAGTGGTGCGATCTCGGCTCTCTGCAAGCTCCGCCTCCCGGGTTCATGCCATT A T DRG1 Ensembl:ENSG00000185721 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1452698835 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113269,RMVar_hsa_circ_213802,RMVar_hsa_circ_120142,RMVar_hsa_circ_111920,RMVar_hsa_circ_213803,RMVar_hsa_circ_213807,RMVar_hsa_circ_75970,RMVar_hsa_circ_213808,RMVar_hsa_circ_97896,RMVar_hsa_circ_213812,RMVar_hsa_circ_118211,RMVar_hsa_circ_213813,RMVar_hsa_circ_101481,RMVar_hsa_circ_95976,RMVar_hsa_circ_213814,RMVar_hsa_circ_213815 33195 RMVar_ID_33195 Human_SNP_ID_701890465 A-to-I Human chr22 + 31434985 31434985 31434985 CCTGTGTCAGCCTCCTGATTAGCTGGGATTACAGGCAGGTACCACCATGCCCCGCTAATTTTGTA CCTGTGTCAGCCTCCTGATTAGCTGGGATTACGGGCAGGTACCACCATGCCCCGCTAATTTTGTA A G DRG1 Ensembl:ENSG00000185721 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs972975061 Functional Loss SNV dbSNP153 33..33 33 - - - 33196 RMVar_ID_33196 Human_SNP_ID_701890584 A-to-I Human chr22 + 31435476 31435476 31435476 GGGTAACAATATGGACGGAGGGGGCTGGGCCCAGTAGCTCACACCTGTAATCCCAGCACTTTGGG GGGTAACAATATGGACGGAGGGGGCTGGGCCCCGTAGCTCACACCTGTAATCCCAGCACTTTGGG A C DRG1 Ensembl:ENSG00000185721 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1267791887 Functional Loss SNV dbSNP153 33..33 33 - - - 33197 RMVar_ID_33197 Human_SNP_ID_701890585 A-to-I Human chr22 + 31435479 31435479 31435479 TAACAATATGGACGGAGGGGGCTGGGCCCAGTAGCTCACACCTGTAATCCCAGCACTTTGGGAGG TAACAATATGGACGGAGGGGGCTGGGCCCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGG A G DRG1 Ensembl:ENSG00000185721 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1261238474 Functional Loss SNV dbSNP153 33..33 33 - - - 33198 RMVar_ID_33198 Human_SNP_ID_701890635 A-to-I Human chr22 + 31435689 31435689 31435689 AGGACTGCTTGAGCCTGGGAGGTCCAGGCTGCAGTGAGCTAAGATGGGCCACTGCACTCCAGCCT AGGACTGCTTGAGCCTGGGAGGTCCAGGCTGCCGTGAGCTAAGATGGGCCACTGCACTCCAGCCT A C DRG1 Ensembl:ENSG00000185721 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1023892399 Functional Loss SNV dbSNP153 33..33 33 - - - 33199 RMVar_ID_33199 Human_SNP_ID_701890636 A-to-I Human chr22 + 31435689 31435689 31435689 AGGACTGCTTGAGCCTGGGAGGTCCAGGCTGCAGTGAGCTAAGATGGGCCACTGCACTCCAGCCT AGGACTGCTTGAGCCTGGGAGGTCCAGGCTGCGGTGAGCTAAGATGGGCCACTGCACTCCAGCCT A G DRG1 Ensembl:ENSG00000185721 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1023892399 Functional Loss SNV dbSNP153 33..33 33 - - - 33200 RMVar_ID_33200 Human_SNP_ID_701893048 A-to-I Human chr22 + 31443949 31443949 31443949 CCCGAGTATAGCTGGGACCACAGATGTGCACCACCATGCCCGACTAATTTTTTGTATTAGGGGTA CCCGAGTATAGCTGGGACCACAGATGTGCACCGCCATGCCCGACTAATTTTTTGTATTAGGGGTA A G DRG1 Ensembl:ENSG00000185721 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1241307462 Functional Loss SNV dbSNP153 33..33 33 - - - 33201 RMVar_ID_33201 Human_SNP_ID_701893058 A-to-I Human chr22 + 31443975 31443974 31443975 TGCACCACCATGCCCGACTAATTTTTTGTATTAGGGGTAGAGACAGGGTCTCACTAGGTTGCCCA TGCACCACCATGCCCGACTAATTTTTTGTATT_GGGGTAGAGACAGGGTCTCACTAGGTTGCCCA TA T DRG1 Ensembl:ENSG00000185721 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1316856376 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_7075752,Human_RBP_ID_14459110 33202 RMVar_ID_33202 Human_SNP_ID_701893075 A-to-I Human chr22 + 31444045 31444038 31444046 GTCTTGAACTCCTGAACTCAAACAATCTACCTACCTCGGCCTCTGAAAGTCCTGGGATTACAGGC GTCTTGAACTCCTGAACTCAAACAAT________CTCGGCCTCTGAAAGTCCTGGGATTACAGGC TCTACCTAC T DRG1 Ensembl:ENSG00000185721 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs932331019 Functional Loss DEL dbSNP153 27..34 33 - - - Human_RBP_ID_14459113 33203 RMVar_ID_33203 Human_SNP_ID_701904011 A-to-I Human chr22 - 31483338 31483338 31483338 AAATTAGCTAGGTATGGTGGCGTATTGCCTGTAGTCTCAGCTACACAGGGGACTGAGGTGAGAGA AAATTAGCTAGGTATGGTGGCGTATTGCCTGTCGTCTCAGCTACACAGGGGACTGAGGTGAGAGA T G EIF4ENIF1 Ensembl:ENSG00000184708 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs970491178 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58836,RMVar_hsa_circ_63188,RMVar_hsa_circ_65513,RMVar_hsa_circ_22968 33204 RMVar_ID_33204 Human_SNP_ID_701904543 A-to-I Human chr22 - 31485614 31485614 31485614 GTTGGTCAGTCCTGTCTTGAACTCCTGACCTCAGGTGATCCACCCACCTCAGCCTTCCAAAGTGC GTTGGTCAGTCCTGTCTTGAACTCCTGACCTCGGGTGATCCACCCACCTCAGCCTTCCAAAGTGC T C EIF4ENIF1 Ensembl:ENSG00000184708 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005801946 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14459664 RMVar_hsa_circ_58836,RMVar_hsa_circ_63188,RMVar_hsa_circ_65513,RMVar_hsa_circ_22968 33205 RMVar_ID_33205 Human_SNP_ID_701914549 A-to-I Human chr22 + 31520897 31520897 31520897 GTGGTAGTGCTTGCCTGTAGTACCAGCTGCTCAGGAGTCTAAAGTGGGAGGATCACGTGAGCCTG GTGGTAGTGCTTGCCTGTAGTACCAGCTGCTCGGGAGTCTAAAGTGGGAGGATCACGTGAGCCTG A G SFI1,DRG1 Ensembl:ENSG00000198089,Ensembl:ENSG00000185721 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1445788851 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6488,RMVar_hsa_circ_354697,RMVar_hsa_circ_356260,RMVar_hsa_circ_345818,RMVar_hsa_circ_74337,RMVar_hsa_circ_213835 33206 RMVar_ID_33206 Human_SNP_ID_701922065 A-to-I Human chr22 + 31549229 31549229 31549229 GGAGTACCTGAGCCCAGGGAGGGCTCAAGGCTACAGTGAGCCATGTTCACATTACTGTACTCCAG GGAGTACCTGAGCCCAGGGAGGGCTCAAGGCTGCAGTGAGCCATGTTCACATTACTGTACTCCAG A G SFI1 Ensembl:ENSG00000198089 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1037948103 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_528,RMVar_hsa_circ_6488,RMVar_hsa_circ_992,RMVar_hsa_circ_74337,RMVar_hsa_circ_357552,RMVar_hsa_circ_43878,RMVar_hsa_circ_69471,RMVar_hsa_circ_321039,RMVar_hsa_circ_297414,RMVar_hsa_circ_36395,RMVar_hsa_circ_213838,RMVar_hsa_circ_213839 33207 RMVar_ID_33207 Human_SNP_ID_701922208 A-to-I Human chr22 + 31549599 31549599 31549599 ATTGACCAGGCTGGTCTCGAACTCCCAACCTCAGGTGGTCTGCCTGCCTCAGCCTCCCAGAGTGC ATTGACCAGGCTGGTCTCGAACTCCCAACCTCGGGTGGTCTGCCTGCCTCAGCCTCCCAGAGTGC A G SFI1 Ensembl:ENSG00000198089 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1321787320 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_528,RMVar_hsa_circ_6488,RMVar_hsa_circ_992,RMVar_hsa_circ_74337,RMVar_hsa_circ_357552,RMVar_hsa_circ_43878,RMVar_hsa_circ_69471,RMVar_hsa_circ_321039,RMVar_hsa_circ_297414,RMVar_hsa_circ_36395,RMVar_hsa_circ_213838,RMVar_hsa_circ_213839 33208 RMVar_ID_33208 Human_SNP_ID_701924500 A-to-I Human chr22 + 31558880 31558880 31558880 ACTGTTTCGTCCAGGCTGGAGTGCCATGGCACAATCTTGGCTGACTGCAAGCTCTGCTTCCTGGG ACTGTTTCGTCCAGGCTGGAGTGCCATGGCACGATCTTGGCTGACTGCAAGCTCTGCTTCCTGGG A G SFI1 Ensembl:ENSG00000198089 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1172809269 Functional Loss SNV dbSNP153 33..33 33 - - - 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_213841 33209 RMVar_ID_33209 Human_SNP_ID_701924526 A-to-I Human chr22 + 31559009 31559009 31559009 TTGTATTTTTAGTAGAGATGGGGTTTCACCACATTGGCCAGGCTGGTCTTGAACTCCTGACCTCA TTGTATTTTTAGTAGAGATGGGGTTTCACCACGTTGGCCAGGCTGGTCTTGAACTCCTGACCTCA A G SFI1 Ensembl:ENSG00000198089 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs146846483 Functional Loss SNV dbSNP153 33..33 33 - - - 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_213841 33210 RMVar_ID_33210 Human_SNP_ID_701924560 A-to-I Human chr22 + 31559167 31559154 31559167 GTACTGGGCCAGGCACAGGGACTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCTGGTGA GTACTGGGCCAGGCACAGGG_____________ATCCCAGCACTTTGGGAGGCTGAGGCTGGTGA GACTCATGCCTGTA G SFI1 Ensembl:ENSG00000198089 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs927019421 Functional Loss DEL dbSNP153 21..33 33 - - - 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_213841 33211 RMVar_ID_33211 Human_SNP_ID_701924575 A-to-I Human chr22 + 31559241 31559241 31559241 GGCCAGGAGTTTAAGACCAGCCTGGCCAACATAGTGAAACTGTCTCTACTAAAAAAATACAAAAG GGCCAGGAGTTTAAGACCAGCCTGGCCAACATGGTGAAACTGTCTCTACTAAAAAAATACAAAAG A G SFI1 Ensembl:ENSG00000198089 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1250765640 Functional Loss SNV dbSNP153 33..33 33 - - - 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_213841 33212 RMVar_ID_33212 Human_SNP_ID_701927431 A-to-I Human chr22 + 31569818 31569818 31569818 AAAAATACAAAAAATTATCCTGTTATGGTGGCATGTGTCTGTAGTCCCAGCTACTCAGGAGGCTA AAAAATACAAAAAATTATCCTGTTATGGTGGCCTGTGTCTGTAGTCCCAGCTACTCAGGAGGCTA A C SFI1 Ensembl:ENSG00000198089 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1004914699 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 33213 RMVar_ID_33213 Human_SNP_ID_701927432 A-to-I Human chr22 + 31569818 31569818 31569818 AAAAATACAAAAAATTATCCTGTTATGGTGGCATGTGTCTGTAGTCCCAGCTACTCAGGAGGCTA AAAAATACAAAAAATTATCCTGTTATGGTGGCGTGTGTCTGTAGTCCCAGCTACTCAGGAGGCTA A G SFI1 Ensembl:ENSG00000198089 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1004914699 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 33214 RMVar_ID_33214 Human_SNP_ID_701929399 A-to-I Human chr22 + 31577485 31577485 31577485 AGTGGCTTTCACAGGCGCAATGGTAGCTCACTACAGTCTTGAACTCCTGGGCTTAAGCAATCCTC AGTGGCTTTCACAGGCGCAATGGTAGCTCACTGCAGTCTTGAACTCCTGGGCTTAAGCAATCCTC A G SFI1 Ensembl:ENSG00000198089 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1225636749 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14839,RMVar_hsa_circ_43878,RMVar_hsa_circ_266413,RMVar_hsa_circ_47576,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_102474,RMVar_hsa_circ_345147,RMVar_hsa_circ_213841,RMVar_hsa_circ_264976,RMVar_hsa_circ_213844,RMVar_hsa_circ_35834,RMVar_hsa_circ_330616 33215 RMVar_ID_33215 Human_SNP_ID_701936723 A-to-I Human chr22 + 31600088 31600088 31600088 CGATTGATTGATTGTAGAGACGAGGTCTCACTATGCTGCCCAGGCTGGTTTTGAACTCCTGAGTT CGATTGATTGATTGTAGAGACGAGGTCTCACTTTGCTGCCCAGGCTGGTTTTGAACTCCTGAGTT A T SFI1 Ensembl:ENSG00000198089 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs981081689 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23943641 RMVar_hsa_circ_43167,RMVar_hsa_circ_213842,RMVar_hsa_circ_27357,RMVar_hsa_circ_27988,RMVar_hsa_circ_12484,RMVar_hsa_circ_102474,RMVar_hsa_circ_213841,RMVar_hsa_circ_264976,RMVar_hsa_circ_213844,RMVar_hsa_circ_6070,RMVar_hsa_circ_213847,RMVar_hsa_circ_319542,RMVar_hsa_circ_322163,RMVar_hsa_circ_365033,RMVar_hsa_circ_318127,RMVar_hsa_circ_280528,RMVar_hsa_circ_299275,RMVar_hsa_circ_17485,RMVar_hsa_circ_213845,RMVar_hsa_circ_213846,RMVar_hsa_circ_346921,RMVar_hsa_circ_363468,RMVar_hsa_circ_299478,RMVar_hsa_circ_317847,RMVar_hsa_circ_38348,RMVar_hsa_circ_213849,RMVar_hsa_circ_213850,RMVar_hsa_circ_213851,RMVar_hsa_circ_316216 33216 RMVar_ID_33216 Human_SNP_ID_701938650 A-to-I Human chr22 + 31606827 31606827 31606827 CAAGCGATTTCTCCTGCCTCAACCTCCCGAGTAGCTGGGACTACAGGCTTGCGCCACCACGTCCG CAAGCGATTTCTCCTGCCTCAACCTCCCGAGTTGCTGGGACTACAGGCTTGCGCCACCACGTCCG A T SFI1 Ensembl:ENSG00000198089 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1462363959 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43167,RMVar_hsa_circ_27988,RMVar_hsa_circ_213841,RMVar_hsa_circ_264976,RMVar_hsa_circ_213847,RMVar_hsa_circ_319542,RMVar_hsa_circ_280528,RMVar_hsa_circ_213846,RMVar_hsa_circ_317847,RMVar_hsa_circ_38348,RMVar_hsa_circ_31404,RMVar_hsa_circ_213850,RMVar_hsa_circ_85994,RMVar_hsa_circ_213854,RMVar_hsa_circ_213852,RMVar_hsa_circ_67472,RMVar_hsa_circ_40224,RMVar_hsa_circ_326223 33217 RMVar_ID_33217 Human_SNP_ID_701938654 A-to-I Human chr22 + 31606837 31606837 31606837 CTCCTGCCTCAACCTCCCGAGTAGCTGGGACTACAGGCTTGCGCCACCACGTCCGACTAATTTTT CTCCTGCCTCAACCTCCCGAGTAGCTGGGACTCCAGGCTTGCGCCACCACGTCCGACTAATTTTT A C SFI1 Ensembl:ENSG00000198089 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1043303528 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43167,RMVar_hsa_circ_27988,RMVar_hsa_circ_213841,RMVar_hsa_circ_264976,RMVar_hsa_circ_213847,RMVar_hsa_circ_319542,RMVar_hsa_circ_280528,RMVar_hsa_circ_213846,RMVar_hsa_circ_317847,RMVar_hsa_circ_38348,RMVar_hsa_circ_31404,RMVar_hsa_circ_213850,RMVar_hsa_circ_85994,RMVar_hsa_circ_213854,RMVar_hsa_circ_213852,RMVar_hsa_circ_67472,RMVar_hsa_circ_40224,RMVar_hsa_circ_326223 33218 RMVar_ID_33218 Human_SNP_ID_701938679 A-to-I Human chr22 + 31606950 31606950 31606950 GAACTGATGACCTCAGGTGATCCATCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCTCTTT GAACTGATGACCTCAGGTGATCCATCTGCCTCCGCCTCCCAAAGTGCTGGGATTACAGGCTCTTT A C SFI1 Ensembl:ENSG00000198089 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1381224299 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43167,RMVar_hsa_circ_27988,RMVar_hsa_circ_213841,RMVar_hsa_circ_264976,RMVar_hsa_circ_213847,RMVar_hsa_circ_319542,RMVar_hsa_circ_280528,RMVar_hsa_circ_213846,RMVar_hsa_circ_317847,RMVar_hsa_circ_38348,RMVar_hsa_circ_31404,RMVar_hsa_circ_213850,RMVar_hsa_circ_85994,RMVar_hsa_circ_213854,RMVar_hsa_circ_213852,RMVar_hsa_circ_67472,RMVar_hsa_circ_40224,RMVar_hsa_circ_326223 33219 RMVar_ID_33219 Human_SNP_ID_701938801 A-to-I Human chr22 + 31607441 31607441 31607441 CCTGGCCAACATGGTGAAACTCCGTCTCTACTAAAAATACAGAAATTAGCTGGGTGTGGTGGTGC CCTGGCCAACATGGTGAAACTCCGTCTCTACTGAAAATACAGAAATTAGCTGGGTGTGGTGGTGC A G SFI1 Ensembl:ENSG00000198089 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs931713538 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43167,RMVar_hsa_circ_27988,RMVar_hsa_circ_213841,RMVar_hsa_circ_264976,RMVar_hsa_circ_213847,RMVar_hsa_circ_319542,RMVar_hsa_circ_280528,RMVar_hsa_circ_213846,RMVar_hsa_circ_317847,RMVar_hsa_circ_38348,RMVar_hsa_circ_31404,RMVar_hsa_circ_213850,RMVar_hsa_circ_85994,RMVar_hsa_circ_213854,RMVar_hsa_circ_213852,RMVar_hsa_circ_67472,RMVar_hsa_circ_40224,RMVar_hsa_circ_326223 33220 RMVar_ID_33220 Human_SNP_ID_701947756 A-to-I Human chr22 - 31635569 31635569 31635569 AACTCAGCGGGGCATGGTGGCTGACGCCCGTAATCCCAGCACTTTGGGAGGCAGGCAGATCACCT AACTCAGCGGGGCATGGTGGCTGACGCCCGTATTCCCAGCACTTTGGGAGGCAGGCAGATCACCT T A PISD Ensembl:ENSG00000241878 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs902162837 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110554,RMVar_hsa_circ_53036,RMVar_hsa_circ_213859 33221 RMVar_ID_33221 Human_SNP_ID_701947976 A-to-I Human chr22 - 31636500 31636500 31636500 AAATTAGCTGGGCGTGGTGGCGGGTGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAA AAATTAGCTGGGCGTGGTGGCGGGTGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAA T C PISD Ensembl:ENSG00000241878 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1182119744 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110554,RMVar_hsa_circ_53036,RMVar_hsa_circ_213859 33222 RMVar_ID_33222 Human_SNP_ID_701948977 A-to-I Human chr22 - 31638935 31638935 31638935 CAGTCTGGAGTGCAGTGGTGTGAGCAGGGCTCACCACGGCCTCGACCTCCCAGGCTCAGGTGATC CAGTCTGGAGTGCAGTGGTGTGAGCAGGGCTCCCCACGGCCTCGACCTCCCAGGCTCAGGTGATC T G PISD Ensembl:ENSG00000241878 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1034590845 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110554,RMVar_hsa_circ_53036,RMVar_hsa_circ_213859 33223 RMVar_ID_33223 Human_SNP_ID_701949812 A-to-I Human chr22 - 31641696 31641696 31641696 CCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCTTGTGGCACCACACCTGGCTAATTTTTTT CCTGCCTCAGCCTCCCGAGTAGCTGGGATTACCGGCTTGTGGCACCACACCTGGCTAATTTTTTT T G PISD Ensembl:ENSG00000241878 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1569489238 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110554,RMVar_hsa_circ_53036,RMVar_hsa_circ_213859 33224 RMVar_ID_33224 Human_SNP_ID_701949813 A-to-I Human chr22 - 31641708 31641704 31641733 TCAAGCAGTTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCTTGTGGCACCACACCTG TCAAGCAATTTTCCTGCTTCAGCCTCCCAAGTAGGTAGGATTACAGGCTTGTGGCACCACACCTG CAGCTACTCGGGAGGCTGAGGCAGGAGAAC TACCTACTTGGGAGGCTGAAGCAGGAAAAT PISD Ensembl:ENSG00000241878 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs386820690 Functional Loss MNV dbSNP153 8..37 33 - - - RMVar_hsa_circ_110554,RMVar_hsa_circ_53036,RMVar_hsa_circ_213859 33225 RMVar_ID_33225 Human_SNP_ID_701950159 A-to-I Human chr22 - 31642986 31642986 31642986 GCAATTTTCCTGCTTCAGCCTCCCAAGTAGGTAGGATTACAGGTGTGTGCCACCACGCCTGGCTA GCAATTTTCCTGCTTCAGCCTCCCAAGTAGGTGGGATTACAGGTGTGTGCCACCACGCCTGGCTA T C PISD Ensembl:ENSG00000241878 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1249015632 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14460879 RMVar_hsa_circ_110554,RMVar_hsa_circ_53036,RMVar_hsa_circ_213859 33226 RMVar_ID_33226 Human_SNP_ID_701950647 A-to-I Human chr22 - 31644874 31644874 31644874 ATGATCCACCCGCCTCGGCCTCCGAAAGTGCTAGGATTACAGGCGTGAGCCACCATGCCCGGCCA ATGATCCACCCGCCTCGGCCTCCGAAAGTGCTGGGATTACAGGCGTGAGCCACCATGCCCGGCCA T C PISD Ensembl:ENSG00000241878 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs937860858 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110554,RMVar_hsa_circ_53036,RMVar_hsa_circ_213859 33227 RMVar_ID_33227 Human_SNP_ID_701950673 A-to-I Human chr22 - 31644960 31644960 31644960 CTATTACTGCGCCAGCTAATTTTTGTATTTTTAGTAGAGACAGGGGTTCACCCTCTTGGCCAGGC CTATTACTGCGCCAGCTAATTTTTGTATTTTTTGTAGAGACAGGGGTTCACCCTCTTGGCCAGGC T A PISD Ensembl:ENSG00000241878 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1428570417 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14460944 RMVar_hsa_circ_110554,RMVar_hsa_circ_53036,RMVar_hsa_circ_213859 33228 RMVar_ID_33228 Human_SNP_ID_701950757 A-to-I Human chr22 - 31645284 31645284 31645284 CCTCCCACCTCAGCCTTCTGGAGTAGCTGGGAATATAAGCGTGTACCATCCTACCTGGCTAATTT CCTCCCACCTCAGCCTTCTGGAGTAGCTGGGATTATAAGCGTGTACCATCCTACCTGGCTAATTT T A PISD Ensembl:ENSG00000241878 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1296229524 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8548803 RMVar_hsa_circ_110554,RMVar_hsa_circ_53036,RMVar_hsa_circ_213859 33229 RMVar_ID_33229 Human_SNP_ID_701950769 A-to-I Human chr22 - 31645322 31645322 31645322 CGGCTCACTGCATCCCTGACCTCCTAGGCTCAAGCCATCCTCCCACCTCAGCCTTCTGGAGTAGC CGGCTCACTGCATCCCTGACCTCCTAGGCTCAGGCCATCCTCCCACCTCAGCCTTCTGGAGTAGC T C PISD Ensembl:ENSG00000241878 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1029446913 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110554,RMVar_hsa_circ_53036,RMVar_hsa_circ_213859 33230 RMVar_ID_33230 Human_SNP_ID_701950809 A-to-I Human chr22 - 31645448 31645448 31645448 CGCCCACCTCGGCCTCCCAAAGTGTGTGGATTATAGGTGTGCGCCACTGCGCCCGGCCAATTTAT CGCCCACCTCGGCCTCCCAAAGTGTGTGGATTGTAGGTGTGCGCCACTGCGCCCGGCCAATTTAT T C PISD Ensembl:ENSG00000241878 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1469864645 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110554,RMVar_hsa_circ_53036,RMVar_hsa_circ_213859 33231 RMVar_ID_33231 Human_SNP_ID_701950837 A-to-I Human chr22 - 31645533 31645532 31645534 CCTCTACTAAAACTAAAAAAAAAAAAAGAGACAGGGTTTCACCATGTTGGCCAGGCTGCTCTCGA CCTCTACTAAAACTAAAAAAAAAAAAAGAGA__GGGTTTCACCATGTTGGCCAGGCTGCTCTCGA CTG C PISD Ensembl:ENSG00000241878 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1015605525 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_110554,RMVar_hsa_circ_53036,RMVar_hsa_circ_213859 33232 RMVar_ID_33232 Human_SNP_ID_701950838 A-to-I Human chr22 - 31645533 31645533 31645533 CCTCTACTAAAACTAAAAAAAAAAAAAGAGACAGGGTTTCACCATGTTGGCCAGGCTGCTCTCGA CCTCTACTAAAACTAAAAAAAAAAAAAGAGACGGGGTTTCACCATGTTGGCCAGGCTGCTCTCGA T C PISD Ensembl:ENSG00000241878 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1169447399 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110554,RMVar_hsa_circ_53036,RMVar_hsa_circ_213859 33233 RMVar_ID_33233 Human_SNP_ID_701953315 A-to-I Human chr22 - 31655697 31655697 31655697 CCAGGAGGCGGAGGTTGCAGTGAGTTGAGATCACGCCACTGAACTCCAGCCTGGGTGACGGAGCG CCAGGAGGCGGAGGTTGCAGTGAGTTGAGATCCCGCCACTGAACTCCAGCCTGGGTGACGGAGCG T G PISD Ensembl:ENSG00000241878 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1401522801 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_213862,RMVar_hsa_circ_117998 33234 RMVar_ID_33234 Human_SNP_ID_701966305 A-to-I Human chr22 - 31705025 31705025 31705025 GAACTCCTAGGCTGAAGCGATCTGCCCACCTCAGCCTCCCAAAGTGCTGGGATTATAGGCATCAG GAACTCCTAGGCTGAAGCGATCTGCCCACCTCGGCCTCCCAAAGTGCTGGGATTATAGGCATCAG T C PRR14L Ensembl:ENSG00000183530 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1447206376 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14461710 RMVar_hsa_circ_213863,RMVar_hsa_circ_99286,RMVar_hsa_circ_98593,RMVar_hsa_circ_213864,RMVar_hsa_circ_51854,RMVar_hsa_circ_298565,RMVar_hsa_circ_348977,RMVar_hsa_circ_324180,RMVar_hsa_circ_282882,RMVar_hsa_circ_3034,RMVar_hsa_circ_62652,RMVar_hsa_circ_213872 33235 RMVar_ID_33235 Human_SNP_ID_701966524 A-to-I Human chr22 - 31705957 31705957 31705957 TCCCTCTGTCGCCCAGGCTGGAGTGCAGTGGTATAATCTCAGCTTACTACAATCTCCTCCTCCCG TCCCTCTGTCGCCCAGGCTGGAGTGCAGTGGTGTAATCTCAGCTTACTACAATCTCCTCCTCCCG T C PRR14L Ensembl:ENSG00000183530 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1449910808 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_213863,RMVar_hsa_circ_99286,RMVar_hsa_circ_98593,RMVar_hsa_circ_213864,RMVar_hsa_circ_51854,RMVar_hsa_circ_298565,RMVar_hsa_circ_348977,RMVar_hsa_circ_324180,RMVar_hsa_circ_282882,RMVar_hsa_circ_3034,RMVar_hsa_circ_62652,RMVar_hsa_circ_213872 33236 RMVar_ID_33236 Human_SNP_ID_701966593 A-to-I Human chr22 - 31706160 31706158 31706160 TGCCTAGCTAGTTTTTGTATTTTTGTAGAGACAGGGTTTCATCGTGTTGGCCAGGCTGGTCTTGA TGCCTAGCTAGTTTTTGTATTTTTGTAGAGAC__GGTTTCATCGTGTTGGCCAGGCTGGTCTTGA CCT C PRR14L Ensembl:ENSG00000183530 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1484989142 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_213863,RMVar_hsa_circ_99286,RMVar_hsa_circ_98593,RMVar_hsa_circ_213864,RMVar_hsa_circ_51854,RMVar_hsa_circ_298565,RMVar_hsa_circ_348977,RMVar_hsa_circ_324180,RMVar_hsa_circ_282882,RMVar_hsa_circ_3034,RMVar_hsa_circ_62652,RMVar_hsa_circ_213872 33237 RMVar_ID_33237 Human_SNP_ID_701966594 A-to-I Human chr22 - 31706160 31706160 31706160 TGCCTAGCTAGTTTTTGTATTTTTGTAGAGACAGGGTTTCATCGTGTTGGCCAGGCTGGTCTTGA TGCCTAGCTAGTTTTTGTATTTTTGTAGAGACGGGGTTTCATCGTGTTGGCCAGGCTGGTCTTGA T C PRR14L Ensembl:ENSG00000183530 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1235202233 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_213863,RMVar_hsa_circ_99286,RMVar_hsa_circ_98593,RMVar_hsa_circ_213864,RMVar_hsa_circ_51854,RMVar_hsa_circ_298565,RMVar_hsa_circ_348977,RMVar_hsa_circ_324180,RMVar_hsa_circ_282882,RMVar_hsa_circ_3034,RMVar_hsa_circ_62652,RMVar_hsa_circ_213872 33238 RMVar_ID_33238 Human_SNP_ID_701966600 A-to-I Human chr22 - 31706187 31706187 31706187 AGCTGGGATTGCAGGCATGTGCCATCATGCCTAGCTAGTTTTTGTATTTTTGTAGAGACAGGGTT AGCTGGGATTGCAGGCATGTGCCATCATGCCTCGCTAGTTTTTGTATTTTTGTAGAGACAGGGTT T G PRR14L Ensembl:ENSG00000183530 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1329789082 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_213863,RMVar_hsa_circ_99286,RMVar_hsa_circ_98593,RMVar_hsa_circ_213864,RMVar_hsa_circ_51854,RMVar_hsa_circ_298565,RMVar_hsa_circ_348977,RMVar_hsa_circ_324180,RMVar_hsa_circ_282882,RMVar_hsa_circ_3034,RMVar_hsa_circ_62652,RMVar_hsa_circ_213872 33239 RMVar_ID_33239 Human_SNP_ID_701966608 A-to-I Human chr22 - 31706219 31706219 31706219 TCAAGCAATTCTCCTGCCTCACCCTCCCAAGTAGCTGGGATTGCAGGCATGTGCCATCATGCCTA TCAAGCAATTCTCCTGCCTCACCCTCCCAAGTGGCTGGGATTGCAGGCATGTGCCATCATGCCTA T C PRR14L Ensembl:ENSG00000183530 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1344745914 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_213863,RMVar_hsa_circ_99286,RMVar_hsa_circ_98593,RMVar_hsa_circ_213864,RMVar_hsa_circ_51854,RMVar_hsa_circ_298565,RMVar_hsa_circ_348977,RMVar_hsa_circ_324180,RMVar_hsa_circ_282882,RMVar_hsa_circ_3034,RMVar_hsa_circ_62652,RMVar_hsa_circ_213872 33240 RMVar_ID_33240 Human_SNP_ID_701966772 A-to-I Human chr22 - 31706668 31706668 31706668 CCTATAATCCCAACACTTTGGGAGACTGAGGTAGGCAGACCACAAGGTCAGGAGTTCGAGACCAG CCTATAATCCCAACACTTTGGGAGACTGAGGTGGGCAGACCACAAGGTCAGGAGTTCGAGACCAG T C PRR14L Ensembl:ENSG00000183530 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1024110445 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_213863,RMVar_hsa_circ_99286,RMVar_hsa_circ_98593,RMVar_hsa_circ_213864,RMVar_hsa_circ_51854,RMVar_hsa_circ_298565,RMVar_hsa_circ_348977,RMVar_hsa_circ_324180,RMVar_hsa_circ_282882,RMVar_hsa_circ_3034,RMVar_hsa_circ_62652,RMVar_hsa_circ_213872 33241 RMVar_ID_33241 Human_SNP_ID_701967012 A-to-I Human chr22 - 31707680 31707680 31707680 GCACACAGCTTTAAATTGTGTTACTTCCGGCCAGGTGCAGTGGCTCACGCCTGTAATCCCAGCAC GCACACAGCTTTAAATTGTGTTACTTCCGGCCGGGTGCAGTGGCTCACGCCTGTAATCCCAGCAC T C PRR14L Ensembl:ENSG00000183530 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1343152827 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_213863,RMVar_hsa_circ_99286,RMVar_hsa_circ_98593,RMVar_hsa_circ_213864,RMVar_hsa_circ_51854,RMVar_hsa_circ_298565,RMVar_hsa_circ_348977,RMVar_hsa_circ_324180,RMVar_hsa_circ_282882,RMVar_hsa_circ_3034,RMVar_hsa_circ_62652,RMVar_hsa_circ_213872 33242 RMVar_ID_33242 Human_SNP_ID_701967519 A-to-I Human chr22 - 31709450 31709450 31709450 GGAGGCCGAGGCGGGCCTGACCGACGTGGTGAAGCCCTCTCTCTACTACAAATACAAAAAAATTT GGAGGCCGAGGCGGGCCTGACCGACGTGGTGATGCCCTCTCTCTACTACAAATACAAAAAAATTT T A PRR14L Ensembl:ENSG00000183530 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs535293066 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_213863,RMVar_hsa_circ_99286,RMVar_hsa_circ_98593,RMVar_hsa_circ_213864,RMVar_hsa_circ_51854,RMVar_hsa_circ_298565,RMVar_hsa_circ_348977,RMVar_hsa_circ_324180,RMVar_hsa_circ_282882,RMVar_hsa_circ_3034,RMVar_hsa_circ_62652,RMVar_hsa_circ_213872 33243 RMVar_ID_33243 Human_SNP_ID_701967520 A-to-I Human chr22 - 31709450 31709450 31709450 GGAGGCCGAGGCGGGCCTGACCGACGTGGTGAAGCCCTCTCTCTACTACAAATACAAAAAAATTT GGAGGCCGAGGCGGGCCTGACCGACGTGGTGAGGCCCTCTCTCTACTACAAATACAAAAAAATTT T C PRR14L Ensembl:ENSG00000183530 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs535293066 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_213863,RMVar_hsa_circ_99286,RMVar_hsa_circ_98593,RMVar_hsa_circ_213864,RMVar_hsa_circ_51854,RMVar_hsa_circ_298565,RMVar_hsa_circ_348977,RMVar_hsa_circ_324180,RMVar_hsa_circ_282882,RMVar_hsa_circ_3034,RMVar_hsa_circ_62652,RMVar_hsa_circ_213872 33244 RMVar_ID_33244 Human_SNP_ID_701967925 A-to-I Human chr22 - 31710729 31710729 31710729 TAAAGAGTGGCCAGGTATGGTGGCTTACACCTATAATCCCAGCGCTTTGGGAGGCCGAGACAGGT TAAAGAGTGGCCAGGTATGGTGGCTTACACCTGTAATCCCAGCGCTTTGGGAGGCCGAGACAGGT T C PRR14L Ensembl:ENSG00000183530 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1216006261 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25666040 RMVar_hsa_circ_213863,RMVar_hsa_circ_99286,RMVar_hsa_circ_98593,RMVar_hsa_circ_213864,RMVar_hsa_circ_51854,RMVar_hsa_circ_298565,RMVar_hsa_circ_348977,RMVar_hsa_circ_324180,RMVar_hsa_circ_282882,RMVar_hsa_circ_3034,RMVar_hsa_circ_62652,RMVar_hsa_circ_213872 33245 RMVar_ID_33245 Human_SNP_ID_701968101 A-to-I Human chr22 - 31711424 31711424 31711424 TCTTGTCACCCACGCTGGAATGCAGTGGCGCAATCTCGGCTGACCACAACTTCTGCCTCCCGGAT TCTTGTCACCCACGCTGGAATGCAGTGGCGCAGTCTCGGCTGACCACAACTTCTGCCTCCCGGAT T C PRR14L Ensembl:ENSG00000183530 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs978108782 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14461775 RMVar_hsa_circ_213863,RMVar_hsa_circ_99286,RMVar_hsa_circ_98593,RMVar_hsa_circ_213864,RMVar_hsa_circ_51854,RMVar_hsa_circ_298565,RMVar_hsa_circ_348977,RMVar_hsa_circ_324180,RMVar_hsa_circ_282882,RMVar_hsa_circ_3034,RMVar_hsa_circ_62652,RMVar_hsa_circ_213872 33246 RMVar_ID_33246 Human_SNP_ID_701968109 A-to-I Human chr22 - 31711449 31711449 31711449 TATTTATTTTTTGAAACAGTCTCATTCTTGTCACCCACGCTGGAATGCAGTGGCGCAATCTCGGC TATTTATTTTTTGAAACAGTCTCATTCTTGTCGCCCACGCTGGAATGCAGTGGCGCAATCTCGGC T C PRR14L Ensembl:ENSG00000183530 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs564390125 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_213863,RMVar_hsa_circ_99286,RMVar_hsa_circ_98593,RMVar_hsa_circ_213864,RMVar_hsa_circ_51854,RMVar_hsa_circ_298565,RMVar_hsa_circ_348977,RMVar_hsa_circ_324180,RMVar_hsa_circ_282882,RMVar_hsa_circ_3034,RMVar_hsa_circ_62652,RMVar_hsa_circ_213872 33247 RMVar_ID_33247 Human_SNP_ID_701968179 A-to-I Human chr22 - 31711672 31711672 31711672 TCAAGCGATTCTCCTCCTTCAGCCTCCTGAGTAGCTGGGATTACAGGCATGCGCCACCACACCCG TCAAGCGATTCTCCTCCTTCAGCCTCCTGAGTGGCTGGGATTACAGGCATGCGCCACCACACCCG T C PRR14L Ensembl:ENSG00000183530 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1044166937 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_213863,RMVar_hsa_circ_99286,RMVar_hsa_circ_98593,RMVar_hsa_circ_213864,RMVar_hsa_circ_51854,RMVar_hsa_circ_298565,RMVar_hsa_circ_348977,RMVar_hsa_circ_324180,RMVar_hsa_circ_282882,RMVar_hsa_circ_3034,RMVar_hsa_circ_62652,RMVar_hsa_circ_213872 33248 RMVar_ID_33248 Human_SNP_ID_701970668 A-to-I Human chr22 - 31719365 31719365 31719365 CTCTGTTACCCAGGCTGGAGTGCAGTAGTGCAATCACAGCTTATTGCAGCCTTGACGTCCTGGGC CTCTGTTACCCAGGCTGGAGTGCAGTAGTGCAGTCACAGCTTATTGCAGCCTTGACGTCCTGGGC T C PRR14L Ensembl:ENSG00000183530 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs997700065 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_213863,RMVar_hsa_circ_98593,RMVar_hsa_circ_213873,RMVar_hsa_circ_298565,RMVar_hsa_circ_348977,RMVar_hsa_circ_324180,RMVar_hsa_circ_282882,RMVar_hsa_circ_213872,RMVar_hsa_circ_296604,RMVar_hsa_circ_303106,RMVar_hsa_circ_213874 33249 RMVar_ID_33249 Human_SNP_ID_701971956 A-to-I Human chr22 - 31724517 31724517 31724517 ACACACCTGTGGTCCCAGCTACTCGGGAGGCTAAGGCAGAAGGATACTTGAGCCCTGGGAGGTTG ACACACCTGTGGTCCCAGCTACTCGGGAGGCTGAGGCAGAAGGATACTTGAGCCCTGGGAGGTTG T C PRR14L Ensembl:ENSG00000183530 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs568335616 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_213863,RMVar_hsa_circ_98593,RMVar_hsa_circ_213873,RMVar_hsa_circ_298565,RMVar_hsa_circ_348977,RMVar_hsa_circ_324180,RMVar_hsa_circ_282882,RMVar_hsa_circ_213872,RMVar_hsa_circ_296604,RMVar_hsa_circ_303106,RMVar_hsa_circ_213874 33250 RMVar_ID_33250 Human_SNP_ID_701972157 A-to-I Human chr22 - 31725354 31725354 31725354 TATCTTAGTATTGCCCATGGATGTACTTGCACAGTGCACTGCAGCCTCAACCTCCCGGGCTCAAG TATCTTAGTATTGCCCATGGATGTACTTGCACGGTGCACTGCAGCCTCAACCTCCCGGGCTCAAG T C PRR14L Ensembl:ENSG00000183530 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1005098569 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_213863,RMVar_hsa_circ_98593,RMVar_hsa_circ_213873,RMVar_hsa_circ_298565,RMVar_hsa_circ_348977,RMVar_hsa_circ_324180,RMVar_hsa_circ_282882,RMVar_hsa_circ_213872,RMVar_hsa_circ_296604,RMVar_hsa_circ_303106,RMVar_hsa_circ_213874 33251 RMVar_ID_33251 Human_SNP_ID_701972158 A-to-I Human chr22 - 31725354 31725354 31725354 TATCTTAGTATTGCCCATGGATGTACTTGCACAGTGCACTGCAGCCTCAACCTCCCGGGCTCAAG TATCTTAGTATTGCCCATGGATGTACTTGCACCGTGCACTGCAGCCTCAACCTCCCGGGCTCAAG T G PRR14L Ensembl:ENSG00000183530 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1005098569 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_213863,RMVar_hsa_circ_98593,RMVar_hsa_circ_213873,RMVar_hsa_circ_298565,RMVar_hsa_circ_348977,RMVar_hsa_circ_324180,RMVar_hsa_circ_282882,RMVar_hsa_circ_213872,RMVar_hsa_circ_296604,RMVar_hsa_circ_303106,RMVar_hsa_circ_213874 33252 RMVar_ID_33252 Human_SNP_ID_701973494 A-to-I Human chr22 - 31730338 31730338 31730338 CCGGGTCCCGGTTCAAACAGTTTTTCTGCTTCAGCCTCCTGAGTAGCTGGGATTACAGGCACGTG CCGGGTCCCGGTTCAAACAGTTTTTCTGCTTCTGCCTCCTGAGTAGCTGGGATTACAGGCACGTG T A PRR14L Ensembl:ENSG00000183530 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1380222350 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_213873,RMVar_hsa_circ_298565,RMVar_hsa_circ_282882,RMVar_hsa_circ_303106,RMVar_hsa_circ_213876,RMVar_hsa_circ_275382 33253 RMVar_ID_33253 Human_SNP_ID_701973499 A-to-I Human chr22 - 31730355 31730355 31730355 ACTGCAACCTTCGCCTCCCGGGTCCCGGTTCAAACAGTTTTTCTGCTTCAGCCTCCTGAGTAGCT ACTGCAACCTTCGCCTCCCGGGTCCCGGTTCAGACAGTTTTTCTGCTTCAGCCTCCTGAGTAGCT T C PRR14L Ensembl:ENSG00000183530 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1041635780 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1307579,Human_RBP_ID_1382439 RMVar_hsa_circ_213873,RMVar_hsa_circ_298565,RMVar_hsa_circ_282882,RMVar_hsa_circ_303106,RMVar_hsa_circ_213876,RMVar_hsa_circ_275382 33254 RMVar_ID_33254 Human_SNP_ID_701976431 A-to-I Human chr22 - 31740391 31740391 31740391 ACGTGGTGAAACTTTGTCTCTACTAAAAATACAAAAATTAGCTGGGCGTGGTGGCACACGCCTGT ACGTGGTGAAACTTTGTCTCTACTAAAAATACGAAAATTAGCTGGGCGTGGTGGCACACGCCTGT T C PRR14L Ensembl:ENSG00000183530 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1290062518 Functional Loss SNV dbSNP153 33..33 33 - - - 33255 RMVar_ID_33255 Human_SNP_ID_701976497 A-to-I Human chr22 - 31740636 31740636 31740636 AAAGTGTGGGTCAGGCATGGTGACTTGTGCCTATAATCCCAGCACTTTGCGGGGCCAAGGCAGGA AAAGTGTGGGTCAGGCATGGTGACTTGTGCCTGTAATCCCAGCACTTTGCGGGGCCAAGGCAGGA T C PRR14L Ensembl:ENSG00000183530 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1569501026 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5504578,Human_RBP_ID_25680438 33256 RMVar_ID_33256 Human_SNP_ID_701976594 A-to-I Human chr22 - 31741009 31741009 31741009 GACCTCGTGATCCGCCCCTCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCATGCC GACCTCGTGATCCGCCCCTCTCGGCCTCCCAATGTGCTGGGATTACAGGCGTGAGCCACCATGCC T A PRR14L Ensembl:ENSG00000183530 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1243960090 Functional Loss SNV dbSNP153 33..33 33 - - - 33257 RMVar_ID_33257 Human_SNP_ID_701976716 A-to-I Human chr22 - 31741350 31741350 31741350 TCAAGCGATTCTTGTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGAGCCTGCCACCACGCCTG TCAAGCGATTCTTGTGCCTCAGCCTCCCGAGTTGCTGGGATTACAGGAGCCTGCCACCACGCCTG T A PRR14L Ensembl:ENSG00000183530 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1002105035 Functional Loss SNV dbSNP153 33..33 33 - - - 33258 RMVar_ID_33258 Human_SNP_ID_701976744 A-to-I Human chr22 - 31741461 31741461 31741461 TTTGTTTTATTGCTTGTTCTTTTTTTTCTTTGAGATGGGAGTCTTGCTTTGTTGCCCAGGCTGGA TTTGTTTTATTGCTTGTTCTTTTTTTTCTTTGTGATGGGAGTCTTGCTTTGTTGCCCAGGCTGGA T A PRR14L Ensembl:ENSG00000183530 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1375807195 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3671548,Human_RBP_ID_7076361,Human_RBP_ID_14462177 33259 RMVar_ID_33259 Human_SNP_ID_701977058 A-to-I Human chr22 - 31742639 31742639 31742639 TTTTAGGCCAGGTGCAGTGGCTCACACCCTTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGGA TTTTAGGCCAGGTGCAGTGGCTCACACCCTTATTCCCAGCACTTTGGGAGGCCGAGGCGGGCGGA T A PRR14L Ensembl:ENSG00000183530 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1009856422 Functional Loss SNV dbSNP153 33..33 33 - - - 33260 RMVar_ID_33260 Human_SNP_ID_701977171 A-to-I Human chr22 - 31743144 31743144 31743144 GCGCGTGCCACCATGCCCAGCTGATTTTTTGTATTTTTAGTAGAGACGGGGTGTCACCGTGTTAC GCGCGTGCCACCATGCCCAGCTGATTTTTTGTGTTTTTAGTAGAGACGGGGTGTCACCGTGTTAC T C PRR14L Ensembl:ENSG00000183530 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs546520600 Functional Loss SNV dbSNP153 33..33 33 - - - 33261 RMVar_ID_33261 Human_SNP_ID_701977188 A-to-I Human chr22 - 31743219 31743219 31743219 CGGCTCACTGCACCCTCTGCCTCCCAGGTTCAAGTGATTCTCCTGCCTCAGCCTCCAGAGCAGCT CGGCTCACTGCACCCTCTGCCTCCCAGGTTCAGGTGATTCTCCTGCCTCAGCCTCCAGAGCAGCT T C PRR14L Ensembl:ENSG00000183530 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1295503566 Functional Loss SNV dbSNP153 33..33 33 - - - 33262 RMVar_ID_33262 Human_SNP_ID_701977198 A-to-I Human chr22 - 31743245 31743245 31743245 CAGTCTGGAGTGCAGTGGCGCAATCTCGGCTCACTGCACCCTCTGCCTCCCAGGTTCAAGTGATT CAGTCTGGAGTGCAGTGGCGCAATCTCGGCTCCCTGCACCCTCTGCCTCCCAGGTTCAAGTGATT T G PRR14L Ensembl:ENSG00000183530 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1385739782 Functional Loss SNV dbSNP153 33..33 33 - - - 33263 RMVar_ID_33263 Human_SNP_ID_701977201 A-to-I Human chr22 - 31743255 31743255 31743255 TTTTGTCTCCCAGTCTGGAGTGCAGTGGCGCAATCTCGGCTCACTGCACCCTCTGCCTCCCAGGT TTTTGTCTCCCAGTCTGGAGTGCAGTGGCGCAGTCTCGGCTCACTGCACCCTCTGCCTCCCAGGT T C PRR14L Ensembl:ENSG00000183530 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1263989547 Functional Loss SNV dbSNP153 33..33 33 - - - 33264 RMVar_ID_33264 Human_SNP_ID_701977465 A-to-I Human chr22 - 31744229 31744229 31744229 ACTCAGGAGGCTGGGGCGGGAGAATCTCTTGAACCTGGGAGGTGGAGATTGTGGTGAGCTAAGAT ACTCAGGAGGCTGGGGCGGGAGAATCTCTTGACCCTGGGAGGTGGAGATTGTGGTGAGCTAAGAT T G PRR14L Ensembl:ENSG00000183530 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223619517 Functional Loss SNV dbSNP153 33..33 33 - - - 33265 RMVar_ID_33265 Human_SNP_ID_701977474 A-to-I Human chr22 - 31744271 31744271 31744271 AAAATTAGCTGGGTGTGGTGGCAAATGCCTGTAATCCCAGCTACTCAGGAGGCTGGGGCGGGAGA AAAATTAGCTGGGTGTGGTGGCAAATGCCTGTCATCCCAGCTACTCAGGAGGCTGGGGCGGGAGA T G PRR14L Ensembl:ENSG00000183530 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1028238798 Functional Loss SNV dbSNP153 33..33 33 - - - 33266 RMVar_ID_33266 Human_SNP_ID_701977829 A-to-I Human chr22 - 31745725 31745725 31745725 CTCGTGCCTTAGCCTCCCAAGTAGCTGAGATTACAGGCTCCTGCCACCACGCCCAGCTAATTTTT CTCGTGCCTTAGCCTCCCAAGTAGCTGAGATTGCAGGCTCCTGCCACCACGCCCAGCTAATTTTT T C PRR14L Ensembl:ENSG00000183530 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1206961998 Functional Loss SNV dbSNP153 33..33 33 - - - 33267 RMVar_ID_33267 Human_SNP_ID_701977830 A-to-I Human chr22 - 31745738 31745738 31745738 GGTTCAAGCGATTCTCGTGCCTTAGCCTCCCAAGTAGCTGAGATTACAGGCTCCTGCCACCACGC GGTTCAAGCGATTCTCGTGCCTTAGCCTCCCAGGTAGCTGAGATTACAGGCTCCTGCCACCACGC T C PRR14L Ensembl:ENSG00000183530 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs906295929 Functional Loss SNV dbSNP153 33..33 33 - - - 33268 RMVar_ID_33268 Human_SNP_ID_701977998 A-to-I Human chr22 - 31746054 31746054 31746054 TCACTGCCTCGCGCCTGTAGTCCTGGCTGCTTAGGAGGCTGAGGCAGGAGGATTGCTTGAGTCCA TCACTGCCTCGCGCCTGTAGTCCTGGCTGCTTGGGAGGCTGAGGCAGGAGGATTGCTTGAGTCCA T C PRR14L Ensembl:ENSG00000183530 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1261457421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_246716 33269 RMVar_ID_33269 Human_SNP_ID_701982284 A-to-I Human chr22 + 31761123 31761123 31761123 CCTCCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCACCTGCCACCACGCCTGGCTAATTTTTTG CCTCCCTCAGCCTCCCAAGTAGCTGGGACTACTGGCACCTGCCACCACGCCTGGCTAATTTTTTG A T DEPDC5,Z82190.2 Ensembl:ENSG00000100150,Ensembl:ENSG00000285404 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs184927134 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2105,RMVar_hsa_circ_18781,RMVar_hsa_circ_274294,RMVar_hsa_circ_328735,RMVar_hsa_circ_51056,RMVar_hsa_circ_74356,RMVar_hsa_circ_346228,RMVar_hsa_circ_285652,RMVar_hsa_circ_317430,RMVar_hsa_circ_279587,RMVar_hsa_circ_75715,RMVar_hsa_circ_99274,RMVar_hsa_circ_55839,RMVar_hsa_circ_213878,RMVar_hsa_circ_213880,RMVar_hsa_circ_213881,RMVar_hsa_circ_213882,RMVar_hsa_circ_213879 33270 RMVar_ID_33270 Human_SNP_ID_701982298 A-to-I Human chr22 + 31761180 31761180 31761180 ATTTTTTGTATTTTTAGTAGACACGAGGTTTCACCGTGTTAGCCAGGATGGTCTCAATCTCCTGA ATTTTTTGTATTTTTAGTAGACACGAGGTTTCCCCGTGTTAGCCAGGATGGTCTCAATCTCCTGA A C DEPDC5,Z82190.2 Ensembl:ENSG00000100150,Ensembl:ENSG00000285404 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs946188022 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2105,RMVar_hsa_circ_18781,RMVar_hsa_circ_274294,RMVar_hsa_circ_328735,RMVar_hsa_circ_51056,RMVar_hsa_circ_74356,RMVar_hsa_circ_346228,RMVar_hsa_circ_285652,RMVar_hsa_circ_317430,RMVar_hsa_circ_279587,RMVar_hsa_circ_75715,RMVar_hsa_circ_99274,RMVar_hsa_circ_55839,RMVar_hsa_circ_213878,RMVar_hsa_circ_213880,RMVar_hsa_circ_213881,RMVar_hsa_circ_213882,RMVar_hsa_circ_213879 33271 RMVar_ID_33271 Human_SNP_ID_701982299 A-to-I Human chr22 + 31761180 31761180 31761180 ATTTTTTGTATTTTTAGTAGACACGAGGTTTCACCGTGTTAGCCAGGATGGTCTCAATCTCCTGA ATTTTTTGTATTTTTAGTAGACACGAGGTTTCGCCGTGTTAGCCAGGATGGTCTCAATCTCCTGA A G DEPDC5,Z82190.2 Ensembl:ENSG00000100150,Ensembl:ENSG00000285404 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs946188022 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2105,RMVar_hsa_circ_18781,RMVar_hsa_circ_274294,RMVar_hsa_circ_328735,RMVar_hsa_circ_51056,RMVar_hsa_circ_74356,RMVar_hsa_circ_346228,RMVar_hsa_circ_285652,RMVar_hsa_circ_317430,RMVar_hsa_circ_279587,RMVar_hsa_circ_75715,RMVar_hsa_circ_99274,RMVar_hsa_circ_55839,RMVar_hsa_circ_213878,RMVar_hsa_circ_213880,RMVar_hsa_circ_213881,RMVar_hsa_circ_213882,RMVar_hsa_circ_213879 33272 RMVar_ID_33272 Human_SNP_ID_701982558 A-to-I Human chr22 + 31762073 31762073 31762073 GAGTTCCTGACACCTTGACCTCCCAAAGTGCTAAGATTGCAGGTGTGATCCACCACATCTGTCCC GAGTTCCTGACACCTTGACCTCCCAAAGTGCTGAGATTGCAGGTGTGATCCACCACATCTGTCCC A G DEPDC5,Z82190.2 Ensembl:ENSG00000100150,Ensembl:ENSG00000285404 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1193800950 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2105,RMVar_hsa_circ_18781,RMVar_hsa_circ_274294,RMVar_hsa_circ_328735,RMVar_hsa_circ_51056,RMVar_hsa_circ_74356,RMVar_hsa_circ_346228,RMVar_hsa_circ_285652,RMVar_hsa_circ_317430,RMVar_hsa_circ_279587,RMVar_hsa_circ_75715,RMVar_hsa_circ_99274,RMVar_hsa_circ_55839,RMVar_hsa_circ_213878,RMVar_hsa_circ_213880,RMVar_hsa_circ_213881,RMVar_hsa_circ_213882,RMVar_hsa_circ_213879 33273 RMVar_ID_33273 Human_SNP_ID_701985515 A-to-I Human chr22 + 31772965 31772965 31772965 CACTATGCCCAGCTAATTTTTGTTTTTTTAGTAGACACGGGGTCTTGCCATGTTGGCCAGGCTGG CACTATGCCCAGCTAATTTTTGTTTTTTTAGTGGACACGGGGTCTTGCCATGTTGGCCAGGCTGG A G DEPDC5,Z82190.2 Ensembl:ENSG00000100150,Ensembl:ENSG00000285404 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1349641479 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2105,RMVar_hsa_circ_328735,RMVar_hsa_circ_346228,RMVar_hsa_circ_285652,RMVar_hsa_circ_317430,RMVar_hsa_circ_75715,RMVar_hsa_circ_99274,RMVar_hsa_circ_55839,RMVar_hsa_circ_11012,RMVar_hsa_circ_213880,RMVar_hsa_circ_213881,RMVar_hsa_circ_213882,RMVar_hsa_circ_363730,RMVar_hsa_circ_60398,RMVar_hsa_circ_96311,RMVar_hsa_circ_213883 33274 RMVar_ID_33274 Human_SNP_ID_701988875 A-to-I Human chr22 + 31786114 31786114 31786114 CCCTGTCTCTACTAAAAATACAAAAATTAGCCAGGCGTGGTGGTTGGTGCCTGTAATCCCACTAC CCCTGTCTCTACTAAAAATACAAAAATTAGCCGGGCGTGGTGGTTGGTGCCTGTAATCCCACTAC A G DEPDC5,Z82190.2 Ensembl:ENSG00000100150,Ensembl:ENSG00000285404 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1245846551 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2105,RMVar_hsa_circ_328735,RMVar_hsa_circ_346228,RMVar_hsa_circ_75715,RMVar_hsa_circ_99274,RMVar_hsa_circ_17118,RMVar_hsa_circ_213881,RMVar_hsa_circ_213882,RMVar_hsa_circ_96311,RMVar_hsa_circ_213883,RMVar_hsa_circ_72049,RMVar_hsa_circ_335388,RMVar_hsa_circ_213885,RMVar_hsa_circ_2298,RMVar_hsa_circ_324731,RMVar_hsa_circ_339884,RMVar_hsa_circ_352014,RMVar_hsa_circ_352518,RMVar_hsa_circ_350337,RMVar_hsa_circ_325369,RMVar_hsa_circ_301561,RMVar_hsa_circ_302187,RMVar_hsa_circ_48333,RMVar_hsa_circ_213887,RMVar_hsa_circ_213888,RMVar_hsa_circ_213889,RMVar_hsa_circ_213886,RMVar_hsa_circ_213884 33275 RMVar_ID_33275 Human_SNP_ID_701996754 A-to-I Human chr22 + 31815788 31815788 31815788 CCTGGACTCGAGGGATCCACCCATTGGCCTCCAAAAGTGCTGAGATTACAGGCATGAACCAATGT CCTGGACTCGAGGGATCCACCCATTGGCCTCCGAAAGTGCTGAGATTACAGGCATGAACCAATGT A G DEPDC5,Z82190.2 Ensembl:ENSG00000100150,Ensembl:ENSG00000285404 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1030354893 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75715,RMVar_hsa_circ_99274,RMVar_hsa_circ_213881,RMVar_hsa_circ_213882,RMVar_hsa_circ_96311,RMVar_hsa_circ_213883,RMVar_hsa_circ_2298,RMVar_hsa_circ_48333,RMVar_hsa_circ_213884,RMVar_hsa_circ_350416,RMVar_hsa_circ_8167,RMVar_hsa_circ_65392,RMVar_hsa_circ_35455,RMVar_hsa_circ_75127,RMVar_hsa_circ_314967,RMVar_hsa_circ_327691,RMVar_hsa_circ_322117,RMVar_hsa_circ_286870 33276 RMVar_ID_33276 Human_SNP_ID_702032993 A-to-I Human chr22 + 31956949 31956949 31956949 CTGCACTCCTGTCTCTTGGGAAGCAGTTTCAGATAAATCATGGGCATTGCTGGACTGATGGTTGC CTGCACTCCTGTCTCTTGGGAAGCAGTTTCAGGTAAATCATGGGCATTGCTGGACTGATGGTTGC A G YWHAH Ensembl:ENSG00000128245 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs922224233 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_578585,Human_RBP_ID_1942024,Human_RBP_ID_3671604,Human_RBP_ID_7076610,Human_RBP_ID_8548898,Human_RBP_ID_14462970,Human_RBP_ID_17285698,Human_RBP_ID_17398913,Human_RBP_ID_17514894,Human_RBP_ID_17985064,Human_RBP_ID_18328798 Human_miRNA_ID_891831,Human_miRNA_ID_1378944,Human_miRNA_ID_2496840,Human_miRNA_ID_2498066 RMVar_hsa_circ_126928,RMVar_hsa_circ_213919 33277 RMVar_ID_33277 Human_SNP_ID_702052509 A-to-I Human chr22 - 32039647 32039647 32039647 CCTCTCTGAATCCATTTCATCAGATGCGTGACATAGCCTGCTATCTTGTTGCGGAGCTTCTTGCT CCTCTCTGAATCCATTTCATCAGATGCGTGACGTAGCCTGCTATCTTGTTGCGGAGCTTCTTGCT T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs539008116 Functional Loss SNV dbSNP153 33..33 33 - - - 33278 RMVar_ID_33278 Human_SNP_ID_702110924 A-to-I Human chr22 + 32271425 32271425 32271425 TGGTGCATGTGGACCAAAAGCTGCTTATCTACAAGGCCTTCCCCCACGACTCTCGGCTCAGCCAG TGGTGCATGTGGACCAAAAGCTGCTTATCTACGAGGCCTTCCCCCACGACTCTCGGCTCAGCCAG A G SLC5A4-AS1,CPSF1P1 Ensembl:ENSG00000242082,Ensembl:ENSG00000214076 lincRNA,Pseudogene exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs545167098 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_213921,RMVar_hsa_circ_213922 33279 RMVar_ID_33279 Human_SNP_ID_702111261 A-to-I Human chr22 - 32272622 32272622 32272622 TTCAGGCAGGTACATGTACACCATGAGGCTGCAGTCGTGGTCAGACACCAGAAAACCCAGCTGGG TTCAGGCAGGTACATGTACACCATGAGGCTGCGGTCGTGGTCAGACACCAGAAAACCCAGCTGGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1222687003 Functional Loss SNV dbSNP153 33..33 33 - - - 33280 RMVar_ID_33280 Human_SNP_ID_702111269 A-to-I Human chr22 - 32272651 32272651 32272651 AGGCACATGCCCCCAAAACTCTCCTTGGCTTCAGGCAGGTACATGTACACCATGAGGCTGCAGTC AGGCACATGCCCCCAAAACTCTCCTTGGCTTCGGGCAGGTACATGTACACCATGAGGCTGCAGTC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1276841271 Functional Loss SNV dbSNP153 33..33 33 - - - 33281 RMVar_ID_33281 Human_SNP_ID_702111273 A-to-I Human chr22 - 32272669 32272669 32272669 AAGTCTGCCCAGCGCAGCAGGCACATGCCCCCAAAACTCTCCTTGGCTTCAGGCAGGTACATGTA AAGTCTGCCCAGCGCAGCAGGCACATGCCCCCGAAACTCTCCTTGGCTTCAGGCAGGTACATGTA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1306610568 Functional Loss SNV dbSNP153 33..33 33 - - - 33282 RMVar_ID_33282 Human_SNP_ID_702144990 A-to-I Human chr22 - 32386443 32386437 32386443 TCCCTAGATCTCAACTTTCTCATGGGAATCATAAGAGAGATGAGACCCAGGGTTTTTTCAGTCTC TCCCTAGATCTCAACTTTCTCATGGGAATCAT______GATGAGACCCAGGGTTTTTTCAGTCTC CTCTCTT C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1378885521 Functional Loss DEL dbSNP153 33..38 33 - - - 33283 RMVar_ID_33283 Human_SNP_ID_702144991 A-to-I Human chr22 - 32386443 32386439 32386444 TCCCTAGATCTCAACTTTCTCATGGGAATCATAAGAGAGATGAGACCCAGGGTTTTTTCAGTCTC TCCCTAGATCTCAACTTTCTCATGGGAATCA_____GAGATGAGACCCAGGGTTTTTTCAGTCTC CTCTTA C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1229667495 Functional Loss DEL dbSNP153 32..36 33 - - - 33284 RMVar_ID_33284 Human_SNP_ID_702200993 A-to-I Human chr22 - 32595872 32595872 32595872 GGGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTCCTGACCTCAAGTGATCCACCCGTCATGGC GGGTTTCACCATGTTGGCCAGGCTGGTCTCAATCTCCTGACCTCAAGTGATCCACCCGTCATGGC T A SYN3 Ensembl:ENSG00000185666 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1198689922 Functional Loss SNV dbSNP153 33..33 33 - - - 33285 RMVar_ID_33285 Human_SNP_ID_702251262 A-to-I Human chr22 + 32809437 32809437 32809437 TTCCCTGCTGCCCCCAAATTTTATTACTGTATAGTCAGTTCTGGGATCCTAACATAACCAAGCCT TTCCCTGCTGCCCCCAAATTTTATTACTGTATTGTCAGTTCTGGGATCCTAACATAACCAAGCCT A T TIMP3 Ensembl:ENSG00000100234 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1212505341 Functional Loss SNV dbSNP153 33..33 33 - - - 33286 RMVar_ID_33286 Human_SNP_ID_702251266 A-to-I Human chr22 + 32809460 32809460 32809460 TTACTGTATAGTCAGTTCTGGGATCCTAACATAACCAAGCCTTACCTCCTAACCCAGTGCCCTTT TTACTGTATAGTCAGTTCTGGGATCCTAACATTACCAAGCCTTACCTCCTAACCCAGTGCCCTTT A T TIMP3 Ensembl:ENSG00000100234 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs563695436 Functional Loss SNV dbSNP153 33..33 33 - - - 33287 RMVar_ID_33287 Human_SNP_ID_702319039 A-to-I Human chr22 - 33094843 33094843 33094843 GTGGTGGTGCATGCCTGTAATTCTAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTCAACTCA GTGGTGGTGCATGCCTGTAATTCTAGCTACTCTGGAGGCTGAGGCAGGAGAATCACTTCAACTCA T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs967392669 Functional Loss SNV dbSNP153 33..33 33 - - - 33288 RMVar_ID_33288 Human_SNP_ID_702319040 A-to-I Human chr22 - 33094843 33094843 33094843 GTGGTGGTGCATGCCTGTAATTCTAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTCAACTCA GTGGTGGTGCATGCCTGTAATTCTAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTCAACTCA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs967392669 Functional Loss SNV dbSNP153 33..33 33 - - - 33289 RMVar_ID_33289 Human_SNP_ID_702521098 A-to-I Human chr22 - 33877878 33877878 33877878 TCGCTCTGTTGCTCAGGCTGGAGTGGAGTGGCATGATCTCGGCTCACTGCAGCCTCTGCCTCCCA TCGCTCTGTTGCTCAGGCTGGAGTGGAGTGGCGTGATCTCGGCTCACTGCAGCCTCTGCCTCCCA T C LARGE1 Ensembl:ENSG00000133424 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1483842582 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_213983 33290 RMVar_ID_33290 Human_SNP_ID_702521112 A-to-I Human chr22 - 33877918 33877918 33877918 TATTTTATTATTATTATTATTATTTTTTTGAGACAGAGTCTCGCTCTGTTGCTCAGGCTGGAGTG TATTTTATTATTATTATTATTATTTTTTTGAGTCAGAGTCTCGCTCTGTTGCTCAGGCTGGAGTG T A LARGE1 Ensembl:ENSG00000133424 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1032179384 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_213983 33291 RMVar_ID_33291 Human_SNP_ID_702890364 A-to-I Human chr22 + 35265806 35265806 35265806 TGATATAGAAGCAATCTTTTTTTTTTTTTTTGAGATGGAGTCTCGCTCTGTCGCCCAGGCTGGAG TGATATAGAAGCAATCTTTTTTTTTTTTTTTGTGATGGAGTCTCGCTCTGTCGCCCAGGCTGGAG A T HMGXB4 Ensembl:ENSG00000100281 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1402030509 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_213984,RMVar_hsa_circ_323313,RMVar_hsa_circ_356936,RMVar_hsa_circ_268746,RMVar_hsa_circ_213985,RMVar_hsa_circ_25441 33292 RMVar_ID_33292 Human_SNP_ID_702892781 A-to-I Human chr22 + 35275197 35275197 35275197 GCTGTAGTACAATGGTGCGATCTCAGCTCACTACAACCTCTGCCTCCCGGGTTTAAGTGATTCTC GCTGTAGTACAATGGTGCGATCTCAGCTCACTGCAACCTCTGCCTCCCGGGTTTAAGTGATTCTC A G HMGXB4 Ensembl:ENSG00000100281 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs546911760 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_213984,RMVar_hsa_circ_323313,RMVar_hsa_circ_356936,RMVar_hsa_circ_268746,RMVar_hsa_circ_213985,RMVar_hsa_circ_25441 33293 RMVar_ID_33293 Human_SNP_ID_702893566 A-to-I Human chr22 + 35278790 35278790 35278790 CCCACCTCGGCCTCCTGAGTAGCTGGGGCTACAAGCATGCACCACCACACCCAGCTAATTTTTTA CCCACCTCGGCCTCCTGAGTAGCTGGGGCTACGAGCATGCACCACCACACCCAGCTAATTTTTTA A G HMGXB4 Ensembl:ENSG00000100281 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1228188735 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_213984,RMVar_hsa_circ_323313,RMVar_hsa_circ_356936,RMVar_hsa_circ_268746,RMVar_hsa_circ_213985,RMVar_hsa_circ_25441 33294 RMVar_ID_33294 Human_SNP_ID_702893587 A-to-I Human chr22 + 35278862 35278862 35278862 GTAAAGTTGGAGTCTCACTGTGGCAGCATAGCAAGACTGCATCTCTACAAAAAAAAAAAAAAAAA GTAAAGTTGGAGTCTCACTGTGGCAGCATAGCCAGACTGCATCTCTACAAAAAAAAAAAAAAAAA A C HMGXB4 Ensembl:ENSG00000100281 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1454237801 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_213984,RMVar_hsa_circ_323313,RMVar_hsa_circ_356936,RMVar_hsa_circ_268746,RMVar_hsa_circ_213985,RMVar_hsa_circ_25441 33295 RMVar_ID_33295 Human_SNP_ID_702893632 A-to-I Human chr22 + 35278980 35278980 35278980 GAAGCCAGGGAAACAGTTGAATCCAGGAATTCAAGACTGTAGTGAGCTATGATCGCACCACTGCA GAAGCCAGGGAAACAGTTGAATCCAGGAATTCGAGACTGTAGTGAGCTATGATCGCACCACTGCA A G HMGXB4 Ensembl:ENSG00000100281 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982050204 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14465260,Human_RBP_ID_23312019 RMVar_hsa_circ_213984,RMVar_hsa_circ_323313,RMVar_hsa_circ_356936,RMVar_hsa_circ_268746,RMVar_hsa_circ_213985,RMVar_hsa_circ_25441 33296 RMVar_ID_33296 Human_SNP_ID_702894798 A-to-I Human chr22 + 35283663 35283663 35283663 AATACAAAAATTACCCGGGTGTGGTGGCAGGCACCTGTAATCTCAGCTACTCAGAAGGCTGAGGC AATACAAAAATTACCCGGGTGTGGTGGCAGGCGCCTGTAATCTCAGCTACTCAGAAGGCTGAGGC A G HMGXB4 Ensembl:ENSG00000100281 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1261047485 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_213984,RMVar_hsa_circ_323313,RMVar_hsa_circ_356936,RMVar_hsa_circ_268746,RMVar_hsa_circ_213985,RMVar_hsa_circ_25441 33297 RMVar_ID_33297 Human_SNP_ID_702903851 A-to-I Human chr22 + 35320897 35320897 35320897 TCAGCGTTTTGGGAGGCTGAGGCAGGAGGATCACTTGAGCCCAGGAGTTCCGGGCTACAGCGAGC TCAGCGTTTTGGGAGGCTGAGGCAGGAGGATCTCTTGAGCCCAGGAGTTCCGGGCTACAGCGAGC A T TOM1 Ensembl:ENSG00000100284 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1414254164 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_310650 33298 RMVar_ID_33298 Human_SNP_ID_702922167 A-to-I Human chr22 + 35388193 35388193 35388193 TGGAATCAGAACTGGCTCTCAGGCTCGTGCCTATAATACCAACACTTTGGGAGGCCAAAGCAGGA TGGAATCAGAACTGGCTCTCAGGCTCGTGCCTGTAATACCAACACTTTGGGAGGCCAAAGCAGGA A G HMOX1 Ensembl:ENSG00000100292 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037341191 Functional Loss SNV dbSNP153 33..33 33 - - - 33299 RMVar_ID_33299 Human_SNP_ID_702927623 A-to-I Human chr22 + 35403990 35403990 35403990 AAACAAAGCTAGGTATGCTGGCATATGCCTATAGTCCAGGCTACTTGGAAGGCTGAAGTGGGAGG AAACAAAGCTAGGTATGCTGGCATATGCCTATGGTCCAGGCTACTTGGAAGGCTGAAGTGGGAGG A G MCM5 Ensembl:ENSG00000100297 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1421214724 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14466106 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_214004,RMVar_hsa_circ_214005 33300 RMVar_ID_33300 Human_SNP_ID_702927949 A-to-I Human chr22 + 35405218 35405218 35405218 CGGCTAATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCT CGGCTAATTTTTAGTAGAGATGGGGTTTCACCCTGTTGGCCAGGCTGGTCTCGAACTCCTGACCT A C MCM5 Ensembl:ENSG00000100297 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1364992772 Functional Loss SNV dbSNP153 33..33 33 - - - 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_214004,RMVar_hsa_circ_214005 33301 RMVar_ID_33301 Human_SNP_ID_702927950 A-to-I Human chr22 + 35405218 35405218 35405218 CGGCTAATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCT CGGCTAATTTTTAGTAGAGATGGGGTTTCACCGTGTTGGCCAGGCTGGTCTCGAACTCCTGACCT A G MCM5 Ensembl:ENSG00000100297 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1364992772 Functional Loss SNV dbSNP153 33..33 33 - - - 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_214004,RMVar_hsa_circ_214005 33302 RMVar_ID_33302 Human_SNP_ID_702928132 A-to-I Human chr22 + 35405760 35405760 35405760 GGCCGGGCGCGGTGGCTCATGCCTGTAATCCCAGCATTTTGGGAGGCCGAGGCCAGTGAATTGCC GGCCGGGCGCGGTGGCTCATGCCTGTAATCCCGGCATTTTGGGAGGCCGAGGCCAGTGAATTGCC A G MCM5 Ensembl:ENSG00000100297 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs866675672 Functional Loss SNV dbSNP153 33..33 33 - - - 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_214004,RMVar_hsa_circ_214005 33303 RMVar_ID_33303 Human_SNP_ID_702929031 A-to-I Human chr22 + 35408440 35408440 35408440 AGATCAGGCTGGGCGCCCCAAATGCCCATTGGACCCGTACTTCATCATGCCCGACAAATGCAAAT AGATCAGGCTGGGCGCCCCAAATGCCCATTGGCCCCGTACTTCATCATGCCCGACAAATGCAAAT A C MCM5 Ensembl:ENSG00000100297 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1352901450 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_578939,Human_RBP_ID_929418,Human_RBP_ID_1610666,Human_RBP_ID_14466224,Human_RBP_ID_17285763,Human_RBP_ID_17701894,Human_RBP_ID_18788059,Human_RBP_ID_22820288,Human_RBP_ID_27493455 Human_Splice_Rec_2161648,Human_Splice_Rec_2161680,Human_Splice_Rec_2161718 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_62529,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_90139,RMVar_hsa_circ_214004,RMVar_hsa_circ_267908,RMVar_hsa_circ_268345,RMVar_hsa_circ_214007,RMVar_hsa_circ_369662 33304 RMVar_ID_33304 Human_SNP_ID_702933524 A-to-I Human chr22 + 35424178 35424178 35424178 TCCCACAGAAATACCCGGAGCACGCCATCCACAAGGTGCTGCAGCTCATGCTGCGGCGCGGCGAG TCCCACAGAAATACCCGGAGCACGCCATCCACGAGGTGCTGCAGCTCATGCTGCGGCGCGGCGAG A G MCM5 Ensembl:ENSG00000100297 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935263792 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_65195,Human_RBP_ID_245948,Human_RBP_ID_1029184,Human_RBP_ID_1610754,Human_RBP_ID_4694505,Human_RBP_ID_5119726,Human_RBP_ID_5149003,Human_RBP_ID_17285764,Human_RBP_ID_17514967,Human_RBP_ID_18194084,Human_RBP_ID_27307227 Human_Splice_Rec_2161670,Human_Splice_Rec_2161702 Human_miRNA_ID_43769,Human_miRNA_ID_72487,Human_miRNA_ID_890521,Human_miRNA_ID_1938692,Human_miRNA_ID_1949792,Human_miRNA_ID_2894961 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 33305 RMVar_ID_33305 Human_SNP_ID_702934468 A-to-I Human chr22 + 35427906 35427906 35427906 GTTAAGAACATGGACTTGGGGCCAGGTGTGGTAGCTCATTCCTGTAATCCCAGCACTTTAGGAGG GTTAAGAACATGGACTTGGGGCCAGGTGTGGTGGCTCATTCCTGTAATCCCAGCACTTTAGGAGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1002730787 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7077985,Human_RBP_ID_14466724 33306 RMVar_ID_33306 Human_SNP_ID_702935887 A-to-I Human chr22 + 35433125 35433124 35433126 TCTGGCTTATTTCTTAATTTTCTTGTAGAGACAGGGTCTTGCTATATTGCCCAGGCTAGCCTCAA TCTGGCTTATTTCTTAATTTTCTTGTAGAGAC__GGTCTTGCTATATTGCCCAGGCTAGCCTCAA CAG C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1177543954 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_14466942 33307 RMVar_ID_33307 Human_SNP_ID_702996478 A-to-I Human chr22 + 35659829 35659829 35659829 TCTCTGTTGCCCAGGCTGGAGTGCAGTGGCGTAATCTCGGCTCACTGCAACCTCTGCCTCCTGAG TCTCTGTTGCCCAGGCTGGAGTGCAGTGGCGTCATCTCGGCTCACTGCAACCTCTGCCTCCTGAG A C APOL6 Ensembl:ENSG00000221963 Protein coding 3'UTR GSE38233;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,32596459 RNA-Seq:(High) rs985477734 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76801,RMVar_hsa_circ_82617,RMVar_hsa_circ_125359,RMVar_hsa_circ_214022,RMVar_hsa_circ_214023,RMVar_hsa_circ_214024,RMVar_hsa_circ_214026,RMVar_hsa_circ_97192 33308 RMVar_ID_33308 Human_SNP_ID_702996479 A-to-I Human chr22 + 35659829 35659829 35659829 TCTCTGTTGCCCAGGCTGGAGTGCAGTGGCGTAATCTCGGCTCACTGCAACCTCTGCCTCCTGAG TCTCTGTTGCCCAGGCTGGAGTGCAGTGGCGTGATCTCGGCTCACTGCAACCTCTGCCTCCTGAG A G APOL6 Ensembl:ENSG00000221963 Protein coding 3'UTR GSE38233;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,32596459 RNA-Seq:(High) rs985477734 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76801,RMVar_hsa_circ_82617,RMVar_hsa_circ_125359,RMVar_hsa_circ_214022,RMVar_hsa_circ_214023,RMVar_hsa_circ_214024,RMVar_hsa_circ_214026,RMVar_hsa_circ_97192 33309 RMVar_ID_33309 Human_SNP_ID_702996518 A-to-I Human chr22 + 35659964 35659964 35659964 ATTTTGGTATTTTTTTGTAGAGACAGGGTTTCACCATTTTGGCCAGGCTGGTCTCGAATTCCTGA ATTTTGGTATTTTTTTGTAGAGACAGGGTTTCGCCATTTTGGCCAGGCTGGTCTCGAATTCCTGA A G APOL6 Ensembl:ENSG00000221963 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,29129909,32596459 RNA-Seq:(High) rs1317010668 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125359,RMVar_hsa_circ_214023 33310 RMVar_ID_33310 Human_SNP_ID_702996813 A-to-I Human chr22 + 35661201 35661201 35661201 CAACATGGCAAAACCCTGTCTCTACTATAAATACAAAAATTAGCCAGGTGTAGTGGCAGGGCACT CAACATGGCAAAACCCTGTCTCTACTATAAATTCAAAAATTAGCCAGGTGTAGTGGCAGGGCACT A T APOL6 Ensembl:ENSG00000221963 Protein coding 3'UTR GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,31158229,32596459 RNA-Seq:(High) rs1569135971 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125359,RMVar_hsa_circ_214023 33311 RMVar_ID_33311 Human_SNP_ID_702996816 A-to-I Human chr22 + 35661203 35661203 35661203 ACATGGCAAAACCCTGTCTCTACTATAAATACAAAAATTAGCCAGGTGTAGTGGCAGGGCACTTG ACATGGCAAAACCCTGTCTCTACTATAAATACTAAAATTAGCCAGGTGTAGTGGCAGGGCACTTG A T APOL6 Ensembl:ENSG00000221963 Protein coding 3'UTR GSE47997;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,32596459 RNA-Seq:(High) rs1427018885 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125359,RMVar_hsa_circ_214023 33312 RMVar_ID_33312 Human_SNP_ID_702996817 A-to-I Human chr22 + 35661214 35661214 35661214 CCCTGTCTCTACTATAAATACAAAAATTAGCCAGGTGTAGTGGCAGGGCACTTGTAATCCTATCT CCCTGTCTCTACTATAAATACAAAAATTAGCCGGGTGTAGTGGCAGGGCACTTGTAATCCTATCT A G APOL6 Ensembl:ENSG00000221963 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,29129909,32596459 RNA-Seq:(High) rs1176820578 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125359,RMVar_hsa_circ_214023 33313 RMVar_ID_33313 Human_SNP_ID_702996841 A-to-I Human chr22 + 35661278 35661278 35661278 TACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCAGGCTGTAAAGGTTGCAGTGAGCCAAGA TACTCGGGAGGCTGAGGCAGGAGAATCGCTTGCACCCAGGCTGTAAAGGTTGCAGTGAGCCAAGA A C APOL6 Ensembl:ENSG00000221963 Protein coding 3'UTR GSE47997;GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T1 cell line - 23474544,24183664,31158229,31158229 RNA-Seq:(High) rs1269360560 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125359,RMVar_hsa_circ_214023 33314 RMVar_ID_33314 Human_SNP_ID_702996844 A-to-I Human chr22 + 35661290 35661290 35661290 TGAGGCAGGAGAATCGCTTGAACCCAGGCTGTAAAGGTTGCAGTGAGCCAAGATCATGCCACTGC TGAGGCAGGAGAATCGCTTGAACCCAGGCTGTTAAGGTTGCAGTGAGCCAAGATCATGCCACTGC A T APOL6 Ensembl:ENSG00000221963 Protein coding 3'UTR GSE47997;GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line - 23474544,24183664,31158229 RNA-Seq:(High) rs1398089395 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125359,RMVar_hsa_circ_214023 33315 RMVar_ID_33315 Human_SNP_ID_702996850 A-to-I Human chr22 + 35661307 35661307 35661307 TTGAACCCAGGCTGTAAAGGTTGCAGTGAGCCAAGATCATGCCACTGCACTCCAGTCTGGGTGTC TTGAACCCAGGCTGTAAAGGTTGCAGTGAGCCGAGATCATGCCACTGCACTCCAGTCTGGGTGTC A G APOL6 Ensembl:ENSG00000221963 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs3180715 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125359,RMVar_hsa_circ_214023 33316 RMVar_ID_33316 Human_SNP_ID_702996853 A-to-I Human chr22 + 35661313 35661313 35661313 CCAGGCTGTAAAGGTTGCAGTGAGCCAAGATCATGCCACTGCACTCCAGTCTGGGTGTCAGAATG CCAGGCTGTAAAGGTTGCAGTGAGCCAAGATCGTGCCACTGCACTCCAGTCTGGGTGTCAGAATG A G APOL6 Ensembl:ENSG00000221963 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs5755832 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1062171 GWAS_ID_3618,GWAS_ID_3619,GWAS_ID_3620,GWAS_ID_3621,GWAS_ID_3622,GWAS_ID_3623,GWAS_ID_3624,GWAS_ID_3625,GWAS_ID_3626,GWAS_ID_3627,GWAS_ID_3628,GWAS_ID_3629,GWAS_ID_3630,GWAS_ID_3631,GWAS_ID_3632,GWAS_ID_3633,GWAS_ID_3634,GWAS_ID_3635,GWAS_ID_3636,GWAS_ID_3637,GWAS_ID_3638,GWAS_ID_3639,GWAS_ID_3640,GWAS_ID_3641,GWAS_ID_3642,GWAS_ID_3643,GWAS_ID_3644,GWAS_ID_3645,GWAS_ID_3646,GWAS_ID_3647 RMVar_hsa_circ_125359,RMVar_hsa_circ_214023 33317 RMVar_ID_33317 Human_SNP_ID_703062677 A-to-I Human chr22 - 35930750 35930750 35930750 TCTTGGCTTACTGCAACCTCCGCCTCCTGGGTACAAGTGATTCTTGTGCCTCATCCTCCCCTGTA TCTTGGCTTACTGCAACCTCCGCCTCCTGGGTGCAAGTGATTCTTGTGCCTCATCCTCCCCTGTA T C RBFOX2 Ensembl:ENSG00000100320 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1325905800 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_337746 33318 RMVar_ID_33318 Human_SNP_ID_703110653 A-to-I Human chr22 - 36122713 36122713 36122713 CTCCTGCCTCAGCCTCCCAACTAGCTAGGACTACAGGCATGCACCACCATGCCCGGCTAATTTTG CTCCTGCCTCAGCCTCCCAACTAGCTAGGACTGCAGGCATGCACCACCATGCCCGGCTAATTTTG T C lnc-APOL3-2,lnc-APOL3-2:2 RNACentral:URS00008B61AC,RNACentral:URS00008BFFAA lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1224688408 Functional Loss SNV dbSNP153 33..33 33 - - - 33319 RMVar_ID_33319 Human_SNP_ID_703149639 A-to-I Human chr22 + 36266146 36266146 36266146 CAGAGTCTTGCTCTGTCGCCAAGTTGGAGTGCAATGGTGCGATCTCAGCTCACTGCAAGCTCTGC CAGAGTCTTGCTCTGTCGCCAAGTTGGAGTGCGATGGTGCGATCTCAGCTCACTGCAAGCTCTGC A G APOL1 Ensembl:ENSG00000100342 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;HepG2 cell line - 23474544,24183664,29129909,29129909 RNA-Seq:(High) rs1371151801 Functional Loss SNV dbSNP153 33..33 33 - - - 33320 RMVar_ID_33320 Human_SNP_ID_703149645 A-to-I Human chr22 + 36266160 36266160 36266160 GTCGCCAAGTTGGAGTGCAATGGTGCGATCTCAGCTCACTGCAAGCTCTGCCTCCCGTGTTCAAG GTCGCCAAGTTGGAGTGCAATGGTGCGATCTCGGCTCACTGCAAGCTCTGCCTCCCGTGTTCAAG A G APOL1 Ensembl:ENSG00000100342 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879170742 Functional Loss SNV dbSNP153 33..33 33 - - - 33321 RMVar_ID_33321 Human_SNP_ID_703149662 A-to-I Human chr22 + 36266230 36266230 36266230 CTCCTGCCTTGGCCTCCCAAGTAGCTGGGACTACAGGCGCCTACCACCATGCCCAGCTAATTTTT CTCCTGCCTTGGCCTCCCAAGTAGCTGGGACTGCAGGCGCCTACCACCATGCCCAGCTAATTTTT A G APOL1 Ensembl:ENSG00000100342 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1569534203 Functional Loss SNV dbSNP153 33..33 33 - - - 33322 RMVar_ID_33322 Human_SNP_ID_703149670 A-to-I Human chr22 + 36266252 36266252 36266252 AGCTGGGACTACAGGCGCCTACCACCATGCCCAGCTAATTTTTGTATTTTTAATAGAGATGGGGT AGCTGGGACTACAGGCGCCTACCACCATGCCCGGCTAATTTTTGTATTTTTAATAGAGATGGGGT A G APOL1 Ensembl:ENSG00000100342 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1437282697 Functional Loss SNV dbSNP153 33..33 33 - - - 33323 RMVar_ID_33323 Human_SNP_ID_703149694 A-to-I Human chr22 + 36266336 36266336 36266336 TGGTCTCGATCTCCTGACCTCTTGATCTGCCCACCTTGGCCTCCCAAAGTGCTGGGATTACAGGC TGGTCTCGATCTCCTGACCTCTTGATCTGCCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGC A G APOL1 Ensembl:ENSG00000100342 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs969816803 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_153056 33324 RMVar_ID_33324 Human_SNP_ID_703149771 A-to-I Human chr22 + 36266650 36266650 36266650 TTGGGGGGCCGGGTGTAGTGGCTCATGCCTGTAATCCGAGCACTTTGGGAGGCCAAGGCGGGCGG TTGGGGGGCCGGGTGTAGTGGCTCATGCCTGTCATCCGAGCACTTTGGGAGGCCAAGGCGGGCGG A C APOL1 Ensembl:ENSG00000100342 Protein coding 3'UTR GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-Seq:(High) rs1136307 Functional Loss SNV dbSNP153 33..33 33 - - - 33325 RMVar_ID_33325 Human_SNP_ID_703149772 A-to-I Human chr22 + 36266650 36266650 36266650 TTGGGGGGCCGGGTGTAGTGGCTCATGCCTGTAATCCGAGCACTTTGGGAGGCCAAGGCGGGCGG TTGGGGGGCCGGGTGTAGTGGCTCATGCCTGTGATCCGAGCACTTTGGGAGGCCAAGGCGGGCGG A G APOL1 Ensembl:ENSG00000100342 Protein coding 3'UTR GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-Seq:(High) rs1136307 Functional Loss SNV dbSNP153 33..33 33 - - - 33326 RMVar_ID_33326 Human_SNP_ID_703149782 A-to-I Human chr22 + 36266672 36266672 36266672 TCATGCCTGTAATCCGAGCACTTTGGGAGGCCAAGGCGGGCGGATCACGAGGTCAGGAGATCGAG TCATGCCTGTAATCCGAGCACTTTGGGAGGCCGAGGCGGGCGGATCACGAGGTCAGGAGATCGAG A G APOL1 Ensembl:ENSG00000100342 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs140768119 Functional Loss SNV dbSNP153 33..33 33 - - - 33327 RMVar_ID_33327 Human_SNP_ID_703149809 A-to-I Human chr22 + 36266708 36266708 36266708 CGGGCGGATCACGAGGTCAGGAGATCGAGACCATCCTGGCTAACACAGTGAAACCCCGTCTCTAC CGGGCGGATCACGAGGTCAGGAGATCGAGACCCTCCTGGCTAACACAGTGAAACCCCGTCTCTAC A C APOL1 Ensembl:ENSG00000100342 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs571917030 Functional Loss SNV dbSNP153 33..33 33 - - - 33328 RMVar_ID_33328 Human_SNP_ID_703149810 A-to-I Human chr22 + 36266708 36266708 36266708 CGGGCGGATCACGAGGTCAGGAGATCGAGACCATCCTGGCTAACACAGTGAAACCCCGTCTCTAC CGGGCGGATCACGAGGTCAGGAGATCGAGACCGTCCTGGCTAACACAGTGAAACCCCGTCTCTAC A G APOL1 Ensembl:ENSG00000100342 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs571917030 Functional Loss SNV dbSNP153 33..33 33 - - - 33329 RMVar_ID_33329 Human_SNP_ID_703149823 A-to-I Human chr22 + 36266717 36266717 36266717 CACGAGGTCAGGAGATCGAGACCATCCTGGCTAACACAGTGAAACCCCGTCTCTACTAAAAATAC CACGAGGTCAGGAGATCGAGACCATCCTGGCTGACACAGTGAAACCCCGTCTCTACTAAAAATAC A G APOL1 Ensembl:ENSG00000100342 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs766082544 Functional Loss SNV dbSNP153 33..33 33 - - - 33330 RMVar_ID_33330 Human_SNP_ID_703149830 A-to-I Human chr22 + 36266722 36266722 36266722 GGTCAGGAGATCGAGACCATCCTGGCTAACACAGTGAAACCCCGTCTCTACTAAAAATACAAAAA GGTCAGGAGATCGAGACCATCCTGGCTAACACCGTGAAACCCCGTCTCTACTAAAAATACAAAAA A C APOL1 Ensembl:ENSG00000100342 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs189436505 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_153059 33331 RMVar_ID_33331 Human_SNP_ID_703149831 A-to-I Human chr22 + 36266722 36266722 36266722 GGTCAGGAGATCGAGACCATCCTGGCTAACACAGTGAAACCCCGTCTCTACTAAAAATACAAAAA GGTCAGGAGATCGAGACCATCCTGGCTAACACGGTGAAACCCCGTCTCTACTAAAAATACAAAAA A G APOL1 Ensembl:ENSG00000100342 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs189436505 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_153059 33332 RMVar_ID_33332 Human_SNP_ID_703149832 A-to-I Human chr22 + 36266722 36266722 36266722 GGTCAGGAGATCGAGACCATCCTGGCTAACACAGTGAAACCCCGTCTCTACTAAAAATACAAAAA GGTCAGGAGATCGAGACCATCCTGGCTAACACTGTGAAACCCCGTCTCTACTAAAAATACAAAAA A T APOL1 Ensembl:ENSG00000100342 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs189436505 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_153059 33333 RMVar_ID_33333 Human_SNP_ID_703149846 A-to-I Human chr22 + 36266748 36266743 36266749 TAACACAGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTAGCCGGGCATGGTGGCGGGCGCC TAACACAGTGAAACCCCGTCTCTACTAA______AAAAAATTAGCCGGGCATGGTGGCGGGCGCC AAAATAC A APOL1 Ensembl:ENSG00000100342 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1210830303 Functional Loss DEL dbSNP153 29..34 33 - - - 33334 RMVar_ID_33334 Human_SNP_ID_703149850 A-to-I Human chr22 + 36266748 36266748 36266748 TAACACAGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTAGCCGGGCATGGTGGCGGGCGCC TAACACAGTGAAACCCCGTCTCTACTAAAAATCCAAAAAATTAGCCGGGCATGGTGGCGGGCGCC A C APOL1 Ensembl:ENSG00000100342 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs181540965 Functional Loss SNV dbSNP153 33..33 33 - - - 33335 RMVar_ID_33335 Human_SNP_ID_703154245 A-to-I Human chr22 - 36282653 36282653 36282653 GCCAAACCTGCCGAATAAGCCTCTTCTCCTGCAGCCTGAGATGGATGGACAGACAGACACCACAG GCCAAACCTGCCGAATAAGCCTCTTCTCCTGCCGCCTGAGATGGATGGACAGACAGACACCACAG T G MYH9 Ensembl:ENSG00000100345 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1197411496 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_65245,Human_RBP_ID_579190,Human_RBP_ID_8863317,Human_RBP_ID_14474027,Human_RBP_ID_17515017,Human_RBP_ID_23945914,Human_RBP_ID_27307299 Human_miRNA_ID_3063515 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 33336 RMVar_ID_33336 Human_SNP_ID_703154433 A-to-I Human chr22 - 36283277 36283277 36283277 CCGCCTCGGCCTCCCAGAGAGCTGAGATTACAAGGATGAGCCACCGTGCCAGGCCTTCATGGGGC CCGCCTCGGCCTCCCAGAGAGCTGAGATTACAGGGATGAGCCACCGTGCCAGGCCTTCATGGGGC T C MYH9 Ensembl:ENSG00000100345 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1367616465 Functional Loss SNV dbSNP153 33..33 33 - - - 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 33337 RMVar_ID_33337 Human_SNP_ID_703156131 A-to-I Human chr22 - 36288331 36288331 36288331 GGCAGTGGCCGCCCGGAAGAAGCTGGAGATGGACCTGAAGGACCTGGAGGCGCACATCGACTCGG GGCAGTGGCCGCCCGGAAGAAGCTGGAGATGGTCCTGAAGGACCTGGAGGCGCACATCGACTCGG T A MYH9 Ensembl:ENSG00000100345 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1407374239 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_65252,Human_RBP_ID_1068901,Human_RBP_ID_5529921,Human_RBP_ID_8235693,Human_RBP_ID_9392251,Human_RBP_ID_17701910,Human_RBP_ID_18413185,Human_RBP_ID_18535170,Human_RBP_ID_18788344,Human_RBP_ID_22086525,Human_RBP_ID_22455221,Human_RBP_ID_22603506,Human_RBP_ID_26344911,Human_RBP_ID_27036397,Human_RBP_ID_27821643 Human_Splice_Rec_2162512,Human_Splice_Rec_2162513 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_95666,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_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,RMVar_hsa_circ_109262,RMVar_hsa_circ_214070 33338 RMVar_ID_33338 Human_SNP_ID_703161002 A-to-I Human chr22 - 36304064 36304064 36304064 CCGTGCCGGTGTGCTGGCCCACCTGGAGGAGGAGCGAGACCTGAAGATCACCGACGTCATCATAG CCGTGCCGGTGTGCTGGCCCACCTGGAGGAGGGGCGAGACCTGAAGATCACCGACGTCATCATAG T C MYH9 Ensembl:ENSG00000100345 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs778631810 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_65275,Human_RBP_ID_930274,Human_RBP_ID_3963226,Human_RBP_ID_8865728,Human_RBP_ID_9260683,Human_RBP_ID_9300376,Human_RBP_ID_9392310,Human_RBP_ID_27036436 Human_Splice_Rec_2162482,Human_Splice_Rec_2162483,Human_Splice_Rec_2162545 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_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,RMVar_hsa_circ_334055 33339 RMVar_ID_33339 Human_SNP_ID_703170570 A-to-I Human chr22 - 36339175 36339175 36339175 TAAGACTGAGTAATGTGTACTGATGAGGCAGGAGACAGTCTTCAGATCTGGACTTCAGACTGTCT TAAGACTGAGTAATGTGTACTGATGAGGCAGGGGACAGTCTTCAGATCTGGACTTCAGACTGTCT T C MYH9 Ensembl:ENSG00000100345 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928518405 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14474424 RMVar_hsa_circ_20035,RMVar_hsa_circ_114176,RMVar_hsa_circ_47568,RMVar_hsa_circ_214087,RMVar_hsa_circ_96735,RMVar_hsa_circ_112861,RMVar_hsa_circ_305947,RMVar_hsa_circ_116297,RMVar_hsa_circ_102348,RMVar_hsa_circ_214101,RMVar_hsa_circ_214102,RMVar_hsa_circ_214103,RMVar_hsa_circ_214100 33340 RMVar_ID_33340 Human_SNP_ID_703175790 A-to-I Human chr22 - 36358340 36358340 36358340 AGCGTTTGGGCCTGGTGCGGTGGCTGACACCTATAATCCCAGCACTTTGGGAGGCCAAGGCGGGC AGCGTTTGGGCCTGGTGCGGTGGCTGACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGC T C MYH9 Ensembl:ENSG00000100345 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1333099667 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109468,RMVar_hsa_circ_102348,RMVar_hsa_circ_214103,RMVar_hsa_circ_214104 33341 RMVar_ID_33341 Human_SNP_ID_703179139 A-to-I Human chr22 - 36372367 36372367 36372367 CTCCCACCTCAGCCTCCCAAGTAGCTGTGACTACAGGTGCACACCACCACACCTGGCTGATTTTA CTCCCACCTCAGCCTCCCAAGTAGCTGTGACTGCAGGTGCACACCACCACACCTGGCTGATTTTA T C MYH9 Ensembl:ENSG00000100345 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1460572727 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109468,RMVar_hsa_circ_102348,RMVar_hsa_circ_214103,RMVar_hsa_circ_214104 33342 RMVar_ID_33342 Human_SNP_ID_703187440 A-to-I Human chr22 + 36403391 36403391 36403391 TTGTGTGTTTTTTGTAGAGACGAGGTTTCTCTATGTTGGCCAGGCTGGTCTCGAACTCTTCGCCC TTGTGTGTTTTTTGTAGAGACGAGGTTTCTCTGTGTTGGCCAGGCTGGTCTCGAACTCTTCGCCC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1029922455 Functional Loss SNV dbSNP153 33..33 33 - - - 33343 RMVar_ID_33343 Human_SNP_ID_703187441 A-to-I Human chr22 + 36403391 36403391 36403391 TTGTGTGTTTTTTGTAGAGACGAGGTTTCTCTATGTTGGCCAGGCTGGTCTCGAACTCTTCGCCC TTGTGTGTTTTTTGTAGAGACGAGGTTTCTCTTTGTTGGCCAGGCTGGTCTCGAACTCTTCGCCC A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1029922455 Functional Loss SNV dbSNP153 33..33 33 - - - 33344 RMVar_ID_33344 Human_SNP_ID_703210306 A-to-I Human chr22 - 36487909 36487909 36487909 TTTTGTATTTTTAGTAGAGACAGGGTTTCACCACATTGGCCAGGCTGGTCTCGAACTCCTGACCT TTTTGTATTTTTAGTAGAGACAGGGTTTCACCGCATTGGCCAGGCTGGTCTCGAACTCCTGACCT T C FOXRED2 Ensembl:ENSG00000100350 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1363169821 Functional Loss SNV dbSNP153 33..33 33 - - - 33345 RMVar_ID_33345 Human_SNP_ID_703210316 A-to-I Human chr22 - 36487943 36487943 36487943 GGATTACAAGCGCCTGCCACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCAC GGATTACAAGCGCCTGCCACCACGCCCAGCTAGTTTTTGTATTTTTAGTAGAGACAGGGTTTCAC T C FOXRED2 Ensembl:ENSG00000100350 Protein coding 3'UTR GSE47997;GSE126723:GSM3611827,GSM3611828,GSM3611829 K562 cells&HepG2 cells;Bronchiolar epithelium,BEP2D cell line - 23474544,31158229 RNA-Seq:(High) rs1413273673 Functional Loss SNV dbSNP153 33..33 33 - - - 33346 RMVar_ID_33346 Human_SNP_ID_703210329 A-to-I Human chr22 - 36488008 36488007 36488008 GGCTCACTGCAACTTCTGCCTCCCGGGTCTAAACAATTCTCTTCCCTCAACCTCCCAAGTAGCTG GGCTCACTGCAACTTCTGCCTCCCGGGTCTAA_CAATTCTCTTCCCTCAACCTCCCAAGTAGCTG GT G FOXRED2 Ensembl:ENSG00000100350 Protein coding 3'UTR GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line - 29129909,29796672,31158229 RNA-Seq:(High) rs1209307597 Functional Loss DEL dbSNP153 33..33 33 - - - 33347 RMVar_ID_33347 Human_SNP_ID_703210335 A-to-I Human chr22 - 36488029 36488029 36488029 GGAGTGCAATGGCACGATGTCGGCTCACTGCAACTTCTGCCTCCCGGGTCTAAACAATTCTCTTC GGAGTGCAATGGCACGATGTCGGCTCACTGCAGCTTCTGCCTCCCGGGTCTAAACAATTCTCTTC T C FOXRED2 Ensembl:ENSG00000100350 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1234150640 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14475165,Human_RBP_ID_25668286 33348 RMVar_ID_33348 Human_SNP_ID_703210337 A-to-I Human chr22 - 36488035 36488035 36488035 CAGGCTGGAGTGCAATGGCACGATGTCGGCTCACTGCAACTTCTGCCTCCCGGGTCTAAACAATT CAGGCTGGAGTGCAATGGCACGATGTCGGCTCGCTGCAACTTCTGCCTCCCGGGTCTAAACAATT T C FOXRED2 Ensembl:ENSG00000100350 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs376760351 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14475165 33349 RMVar_ID_33349 Human_SNP_ID_703210338 A-to-I Human chr22 - 36488035 36488035 36488035 CAGGCTGGAGTGCAATGGCACGATGTCGGCTCACTGCAACTTCTGCCTCCCGGGTCTAAACAATT CAGGCTGGAGTGCAATGGCACGATGTCGGCTCCCTGCAACTTCTGCCTCCCGGGTCTAAACAATT T G FOXRED2 Ensembl:ENSG00000100350 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs376760351 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14475165 33350 RMVar_ID_33350 Human_SNP_ID_703210459 A-to-I Human chr22 - 36488415 36488415 36488415 TCTCTACTAACGGTAAAAAAAATTAGCTGGGCATGGTGGAGCATGCCTGTCATCCCAGCTACTTG TCTCTACTAACGGTAAAAAAAATTAGCTGGGCGTGGTGGAGCATGCCTGTCATCCCAGCTACTTG T C FOXRED2 Ensembl:ENSG00000100350 Protein coding 3'UTR GSE100210;GSE112787 HepG2 cell line;293 Flip-In T-REx cells,empty vector - 29129909,29967493 RNA-Seq:(High) rs958968811 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25668290 33351 RMVar_ID_33351 Human_SNP_ID_703210464 A-to-I Human chr22 - 36488426 36488425 36488426 GCAAAACCTTGTCTCTACTAACGGTAAAAAAAATTAGCTGGGCATGGTGGAGCATGCCTGTCATC GCAAAACCTTGTCTCTACTAACGGTAAAAAAA_TTAGCTGGGCATGGTGGAGCATGCCTGTCATC AT A FOXRED2 Ensembl:ENSG00000100350 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs112247568 Functional Loss DEL dbSNP153 33..33 33 - - - GWAS_ID_3648,GWAS_ID_3649,GWAS_ID_3650,GWAS_ID_3651,GWAS_ID_3652,GWAS_ID_3653,GWAS_ID_3654,GWAS_ID_3655,GWAS_ID_3656,GWAS_ID_3657,GWAS_ID_3658,GWAS_ID_3659 33352 RMVar_ID_33352 Human_SNP_ID_703210473 A-to-I Human chr22 - 36488461 36488461 36488461 GAGCTCAGGAATTCGAGACCAGCCTGGCCAACATAGCAAAACCTTGTCTCTACTAACGGTAAAAA GAGCTCAGGAATTCGAGACCAGCCTGGCCAACGTAGCAAAACCTTGTCTCTACTAACGGTAAAAA T C FOXRED2 Ensembl:ENSG00000100350 Protein coding 3'UTR GSE47997;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829 K562 cells&HepG2 cells;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;Bronchiolar epithelium,BEP2D cell line - 23474544,30559470,31158229 RNA-Seq:(High) rs778765190 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18788418 33353 RMVar_ID_33353 Human_SNP_ID_703210516 A-to-I Human chr22 - 36488647 36488647 36488647 AACCCGGGAGGCAGAGGTTGCAGTGAGCCGAGATTGCGCCATTGCACTCCAGCCTAGGTAACAAG AACCCGGGAGGCAGAGGTTGCAGTGAGCCGAGGTTGCGCCATTGCACTCCAGCCTAGGTAACAAG T C FOXRED2 Ensembl:ENSG00000100350 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1488426493 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14475175,Human_RBP_ID_22603511,Human_RBP_ID_25668296 33354 RMVar_ID_33354 Human_SNP_ID_703210533 A-to-I Human chr22 - 36488722 36488722 36488722 ACAAAACTAGCCAGGCGTGGTAGCACATGTCTATAATCCCAGCTACTGGAGAGGCTGAGGCAGGA ACAAAACTAGCCAGGCGTGGTAGCACATGTCTGTAATCCCAGCTACTGGAGAGGCTGAGGCAGGA T C FOXRED2 Ensembl:ENSG00000100350 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1011754900 Functional Loss SNV dbSNP153 33..33 33 - - - 33355 RMVar_ID_33355 Human_SNP_ID_703210534 A-to-I Human chr22 - 36488722 36488722 36488722 ACAAAACTAGCCAGGCGTGGTAGCACATGTCTATAATCCCAGCTACTGGAGAGGCTGAGGCAGGA ACAAAACTAGCCAGGCGTGGTAGCACATGTCTCTAATCCCAGCTACTGGAGAGGCTGAGGCAGGA T G FOXRED2 Ensembl:ENSG00000100350 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1011754900 Functional Loss SNV dbSNP153 33..33 33 - - - 33356 RMVar_ID_33356 Human_SNP_ID_703210538 A-to-I Human chr22 - 36488760 36488760 36488760 CCTGACCAACATGGAGAAACCCTATCTCTACTAAAAATACAAAACTAGCCAGGCGTGGTAGCACA CCTGACCAACATGGAGAAACCCTATCTCTACTGAAAATACAAAACTAGCCAGGCGTGGTAGCACA T C FOXRED2 Ensembl:ENSG00000100350 Protein coding 3'UTR GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 29796672,31158229,31158229 RNA-Seq:(High) rs954291308 Functional Loss SNV dbSNP153 33..33 33 - - - 33357 RMVar_ID_33357 Human_SNP_ID_703210541 A-to-I Human chr22 - 36488769 36488769 36488769 TGAGACCAGCCTGACCAACATGGAGAAACCCTATCTCTACTAAAAATACAAAACTAGCCAGGCGT TGAGACCAGCCTGACCAACATGGAGAAACCCTGTCTCTACTAAAAATACAAAACTAGCCAGGCGT T C FOXRED2 Ensembl:ENSG00000100350 Protein coding 3'UTR GSE47997;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,31158229,31158229,31158229 RNA-Seq:(High) rs912579909 Functional Loss SNV dbSNP153 33..33 33 - - - 33358 RMVar_ID_33358 Human_SNP_ID_703210580 A-to-I Human chr22 - 36489032 36489032 36489032 TTTGTGTGATAATGATGATGAATTTGGTTCCTAGTCTCTTCTTCATTGCCCTTCCTCACCAGCAA TTTGTGTGATAATGATGATGAATTTGGTTCCTGGTCTCTTCTTCATTGCCCTTCCTCACCAGCAA T C FOXRED2 Ensembl:ENSG00000100350 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1042185592 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_579277,Human_RBP_ID_1201582,Human_RBP_ID_2717994,Human_RBP_ID_3672308,Human_RBP_ID_8207913,Human_RBP_ID_17286955,Human_RBP_ID_17515042,Human_RBP_ID_18329123,Human_RBP_ID_23946072,Human_RBP_ID_26500977 33359 RMVar_ID_33359 Human_SNP_ID_703211097 A-to-I Human chr22 - 36490945 36490945 36490945 CATTATGTTGGCCAGGCTGGTCTCGAAGTCCTAACCTCAGGCGATCCACCGGCCTCGGCCTCCCA CATTATGTTGGCCAGGCTGGTCTCGAAGTCCTGACCTCAGGCGATCCACCGGCCTCGGCCTCCCA T C FOXRED2 Ensembl:ENSG00000100350 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1236696810 Functional Loss SNV dbSNP153 33..33 33 - - - 33360 RMVar_ID_33360 Human_SNP_ID_703211130 A-to-I Human chr22 - 36491062 36491062 36491062 CGCCTCCTGGATTCGAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGTGTTTG CGCCTCCTGGATTCGAGTGATTCTCCTGCCTCGGCCTCCCGAGTAGCTGGGATTACAGGTGTTTG T C FOXRED2 Ensembl:ENSG00000100350 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1215849480 Functional Loss SNV dbSNP153 33..33 33 - - - 33361 RMVar_ID_33361 Human_SNP_ID_703213338 A-to-I Human chr22 - 36499443 36499443 36499443 TTTGTTGTTTTTATTTTTGTGTGGTAGAGACAAGTTTTCGCCATGTTGCCCAGGCTGGTCTCAAA TTTGTTGTTTTTATTTTTGTGTGGTAGAGACAGGTTTTCGCCATGTTGCCCAGGCTGGTCTCAAA T C FOXRED2 Ensembl:ENSG00000100350 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs889811706 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38278,RMVar_hsa_circ_327875,RMVar_hsa_circ_109631,RMVar_hsa_circ_214118,RMVar_hsa_circ_214119,RMVar_hsa_circ_41047,RMVar_hsa_circ_214120,RMVar_hsa_circ_317347 33362 RMVar_ID_33362 Human_SNP_ID_703217956 A-to-I Human chr22 - 36515441 36515441 36515441 TCACTGCAACCTCTACCTCCCGGGCTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTAGGA TCACTGCAACCTCTACCTCCCGGGCTCAAGCGTTTCTCCTGCCTCAGCCTCCCGAGTAGCTAGGA T A EIF3D Ensembl:ENSG00000100353 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1265683487 Functional Loss SNV dbSNP153 33..33 33 - - - 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_214125 33363 RMVar_ID_33363 Human_SNP_ID_703218642 A-to-I Human chr22 - 36517778 36517778 36517778 ACACCACTGCACTCCAACCTGGGTGACAGAGCAAGACTCCATCTCAAAAAAAAAAGTGTTTATAT ACACCACTGCACTCCAACCTGGGTGACAGAGCTAGACTCCATCTCAAAAAAAAAAGTGTTTATAT T A EIF3D Ensembl:ENSG00000100353 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-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 33364 RMVar_ID_33364 Human_SNP_ID_703218677 A-to-I Human chr22 - 36517927 36517927 36517927 CCTGGCCAACATGGTGAAACCCAGTCTCTACTAAAAATACAAAAATTAGCCAGGTGTGGTGGTGG CCTGGCCAACATGGTGAAACCCAGTCTCTACTGAAAATACAAAAATTAGCCAGGTGTGGTGGTGG T C EIF3D Ensembl:ENSG00000100353 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1392411989 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10051400,Human_RBP_ID_25682367 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 33365 RMVar_ID_33365 Human_SNP_ID_703218782 A-to-I Human chr22 - 36518323 36518323 36518323 CATTACGCCTGGCTACTTTCTATATTTTTAGTAGAGACGGTTTCACCATGTTGGCGAGGCTGGTC CATTACGCCTGGCTACTTTCTATATTTTTAGTGGAGACGGTTTCACCATGTTGGCGAGGCTGGTC T C EIF3D Ensembl:ENSG00000100353 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1174014646 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14475573 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 33366 RMVar_ID_33366 Human_SNP_ID_703218785 A-to-I Human chr22 - 36518326 36518326 36518326 TGCCATTACGCCTGGCTACTTTCTATATTTTTAGTAGAGACGGTTTCACCATGTTGGCGAGGCTG TGCCATTACGCCTGGCTACTTTCTATATTTTTGGTAGAGACGGTTTCACCATGTTGGCGAGGCTG T C EIF3D Ensembl:ENSG00000100353 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1428262608 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14475573,Human_RBP_ID_25668513 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 33367 RMVar_ID_33367 Human_SNP_ID_703218786 A-to-I Human chr22 - 36518334 36518334 36518334 CAGGCATGTGCCATTACGCCTGGCTACTTTCTATATTTTTAGTAGAGACGGTTTCACCATGTTGG CAGGCATGTGCCATTACGCCTGGCTACTTTCTGTATTTTTAGTAGAGACGGTTTCACCATGTTGG T C EIF3D Ensembl:ENSG00000100353 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992968027 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14475573,Human_RBP_ID_25668514 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 33368 RMVar_ID_33368 Human_SNP_ID_703285610 A-to-I Human chr22 - 36775710 36775710 36775710 TCCTCTGGGTACGGCTCGCGGGAGTGTTGGTTACCATGGTGAAGCTGGCAGCCAAATGCATCCTG TCCTCTGGGTACGGCTCGCGGGAGTGTTGGTTTCCATGGTGAAGCTGGCAGCCAAATGCATCCTG T A IFT27 Ensembl:ENSG00000100360 Protein coding 5'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1438370593 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_579396 Human_Splice_Rec_2162819,Human_Splice_Rec_2162843,Human_Splice_Rec_2162853,Human_Splice_Rec_2162859,Human_Splice_Rec_2162868,Human_Splice_Rec_2162869,Human_Splice_Rec_2162879,Human_Splice_Rec_2162883 33369 RMVar_ID_33369 Human_SNP_ID_703352928 A-to-I Human chr22 + 37024705 37024705 37024705 AGTTCCGCGCTCAGCTCGACCCCGCCTTCATCAAGACCTACGAGGACATCAAGGAGAACCTGGAA AGTTCCGCGCTCAGCTCGACCCCGCCTTCATCGAGACCTACGAGGACATCAAGGAGAACCTGGAA A G MPST Ensembl:ENSG00000128309 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) 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 33370 RMVar_ID_33370 Human_SNP_ID_703353565 A-to-I Human chr22 + 37027032 37027032 37027032 TGGAGTACAGTGGCGCAATCTCGGCTCACCACAACCTCCGCCTCCCGGGTTCAAGTGATTCTCCT TGGAGTACAGTGGCGCAATCTCGGCTCACCACGACCTCCGCCTCCCGGGTTCAAGTGATTCTCCT A G MPST Ensembl:ENSG00000128309 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1341540422 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86780,RMVar_hsa_circ_214142 33371 RMVar_ID_33371 Human_SNP_ID_703353598 A-to-I Human chr22 + 37027130 37027129 37027130 ATGTGCCACCACGCCCGGCTAATGTTTGTATTATTAGTAGAGACGGGGTTTCTCCATGTTGGTCA ATGTGCCACCACGCCCGGCTAATGTTTGTATT_TTAGTAGAGACGGGGTTTCTCCATGTTGGTCA TA T MPST Ensembl:ENSG00000128309 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1415600098 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_86780,RMVar_hsa_circ_214142 33372 RMVar_ID_33372 Human_SNP_ID_703353599 A-to-I Human chr22 + 37027130 37027130 37027130 ATGTGCCACCACGCCCGGCTAATGTTTGTATTATTAGTAGAGACGGGGTTTCTCCATGTTGGTCA ATGTGCCACCACGCCCGGCTAATGTTTGTATTGTTAGTAGAGACGGGGTTTCTCCATGTTGGTCA A G MPST Ensembl:ENSG00000128309 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs543203901 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86780,RMVar_hsa_circ_214142 33373 RMVar_ID_33373 Human_SNP_ID_703353825 A-to-I Human chr22 + 37028143 37028143 37028143 CAGCTATTGGCCAGGCAAGGTGGCTTACTCCTATATTCCCAGCACTTTGGGAAGCTGAGGCAGAA CAGCTATTGGCCAGGCAAGGTGGCTTACTCCTGTATTCCCAGCACTTTGGGAAGCTGAGGCAGAA A G MPST Ensembl:ENSG00000128309 Protein coding intron GSE47997;GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 K562 cells&HepG2 cells;cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 23474544,24183664,31158229 RNA-Seq:(High) rs1279685120 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17573173,Human_RBP_ID_25668637 RMVar_hsa_circ_86780,RMVar_hsa_circ_214142 33374 RMVar_ID_33374 Human_SNP_ID_703353842 A-to-I Human chr22 + 37028255 37028255 37028255 AGACCCCATGTCTATAAAAACCAAATTAGGCCAGGCGTGGTGGTTCACACCTGTAATCCCAGCAC AGACCCCATGTCTATAAAAACCAAATTAGGCCGGGCGTGGTGGTTCACACCTGTAATCCCAGCAC A G MPST Ensembl:ENSG00000128309 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs900343786 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86780,RMVar_hsa_circ_214142 33375 RMVar_ID_33375 Human_SNP_ID_703353847 A-to-I Human chr22 + 37028271 37028271 37028271 AAAACCAAATTAGGCCAGGCGTGGTGGTTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGC AAAACCAAATTAGGCCAGGCGTGGTGGTTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGC A G MPST Ensembl:ENSG00000128309 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1284302758 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86780,RMVar_hsa_circ_214142 33376 RMVar_ID_33376 Human_SNP_ID_703353884 A-to-I Human chr22 + 37028471 37028471 37028471 AGAATCACTTGAACCCAGGAGGTGGAGGTTGCAGTAAGCCAAGATCATGCCACTGCACTCCAGCC AGAATCACTTGAACCCAGGAGGTGGAGGTTGCGGTAAGCCAAGATCATGCCACTGCACTCCAGCC A G MPST Ensembl:ENSG00000128309 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1312401696 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25682386 RMVar_hsa_circ_86780,RMVar_hsa_circ_214142 33377 RMVar_ID_33377 Human_SNP_ID_703353885 A-to-I Human chr22 + 37028474 37028474 37028474 ATCACTTGAACCCAGGAGGTGGAGGTTGCAGTAAGCCAAGATCATGCCACTGCACTCCAGCCTGG ATCACTTGAACCCAGGAGGTGGAGGTTGCAGTGAGCCAAGATCATGCCACTGCACTCCAGCCTGG A G MPST Ensembl:ENSG00000128309 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1435536037 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86780,RMVar_hsa_circ_214142 33378 RMVar_ID_33378 Human_SNP_ID_703382448 A-to-I Human chr22 - 37131772 37131771 37131773 AGATGGCACCACTGCACTCCAGCCTGGGCGACAGAGTGAGACTCCATCTCAAAAAAAAAAAAAAA AGATGGCACCACTGCACTCCAGCCTGGGCGA__GAGTGAGACTCCATCTCAAAAAAAAAAAAAAA CTG C IL2RB Ensembl:ENSG00000100385 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1202528419 Functional Loss DEL dbSNP153 32..33 33 - - - 33379 RMVar_ID_33379 Human_SNP_ID_703382486 A-to-I Human chr22 - 37131861 37131861 37131861 CTGGTGGTGCATGCCTGTAATCCCAGCTACTCAGGAGGCTGAGACAGGGGAATCGCTTGAACCCA CTGGTGGTGCATGCCTGTAATCCCAGCTACTCGGGAGGCTGAGACAGGGGAATCGCTTGAACCCA T C IL2RB Ensembl:ENSG00000100385 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1032624272 Functional Loss SNV dbSNP153 33..33 33 - - - 33380 RMVar_ID_33380 Human_SNP_ID_703449112 A-to-I Human chr22 - 37385309 37385309 37385309 TGGAAGCCACTGTGTAGCAGTTGTGAGGCCTCAGTTTCCTCATCTGCAAAGTGGGAATAGTGATA TGGAAGCCACTGTGTAGCAGTTGTGAGGCCTCGGTTTCCTCATCTGCAAAGTGGGAATAGTGATA T C FP325335.1,ELFN2 Ensembl:ENSG00000243902,Ensembl:ENSG00000166897 lincRNA,Protein coding intron,intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1193480036 Functional Loss SNV dbSNP153 33..33 33 - - - 33381 RMVar_ID_33381 Human_SNP_ID_703493566 A-to-I Human chr22 + 37554844 37554844 37554844 ACATAGCGAAACCTCGTCTCTACTAAAAATACAAAAATTAGCTGGGCGTGGTTGCGGACTCCTAT ACATAGCGAAACCTCGTCTCTACTAAAAATACGAAAATTAGCTGGGCGTGGTTGCGGACTCCTAT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1244394173 Functional Loss SNV dbSNP153 33..33 33 - - - 33382 RMVar_ID_33382 Human_SNP_ID_703509500 A-to-I Human chr22 + 37610374 37610374 37610374 GCTTCTTCTTTTTTTTTTTGAGACGGGTTTTCACTCTTGTCACCCAGGCTGGAGTGCAGTGGCAC GCTTCTTCTTTTTTTTTTTGAGACGGGTTTTCGCTCTTGTCACCCAGGCTGGAGTGCAGTGGCAC A G GGA1 Ensembl:ENSG00000100083 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs5995482 Functional Loss SNV dbSNP153 33..33 33 - - - 33383 RMVar_ID_33383 Human_SNP_ID_703509505 A-to-I Human chr22 + 37610407 37610407 37610407 CTCTTGTCACCCAGGCTGGAGTGCAGTGGCACAATCTCAGCTCTCTGCAACCTCCACCTCCCGGG CTCTTGTCACCCAGGCTGGAGTGCAGTGGCACGATCTCAGCTCTCTGCAACCTCCACCTCCCGGG A G GGA1 Ensembl:ENSG00000100083 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs908463204 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2164299 33384 RMVar_ID_33384 Human_SNP_ID_703509539 A-to-I Human chr22 + 37610538 37610538 37610538 TATTTTTGTATTTTTAGTACAGGTGGGCTTTCACCATGTTGGCCAGGCTGATCTCGAACTCCTGA TATTTTTGTATTTTTAGTACAGGTGGGCTTTCGCCATGTTGGCCAGGCTGATCTCGAACTCCTGA A G GGA1 Ensembl:ENSG00000100083 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1440252663 Functional Loss SNV dbSNP153 33..33 33 - - - 33385 RMVar_ID_33385 Human_SNP_ID_703509553 A-to-I Human chr22 + 37610602 37610602 37610602 ACCTCAGGTGATCCGCCTATATAGGCCTCTCAAAGTGTTGGGATTACAGGCGTTAGCCACTCATC ACCTCAGGTGATCCGCCTATATAGGCCTCTCAGAGTGTTGGGATTACAGGCGTTAGCCACTCATC A G GGA1 Ensembl:ENSG00000100083 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992012796 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2164300,Human_Splice_Rec_2164301 33386 RMVar_ID_33386 Human_SNP_ID_703509574 A-to-I Human chr22 + 37610654 37610654 37610654 TTAGCCACTCATCCGCCCACGTCGGCCTCTCAAAGTGTTGGGATTACAGGCGTGAGCCACCGCGC TTAGCCACTCATCCGCCCACGTCGGCCTCTCAGAGTGTTGGGATTACAGGCGTGAGCCACCGCGC A G GGA1 Ensembl:ENSG00000100083 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs779771101 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_246527 Human_Splice_Rec_2164300,Human_Splice_Rec_2164301 33387 RMVar_ID_33387 Human_SNP_ID_703509947 A-to-I Human chr22 + 37611878 37611878 37611878 TTTGTCATCCAAAATCAATATTTTGGTCAGGCACAGTGGCTCATGCCTGTAATCCCAGCACTTTG TTTGTCATCCAAAATCAATATTTTGGTCAGGCGCAGTGGCTCATGCCTGTAATCCCAGCACTTTG A G GGA1 Ensembl:ENSG00000100083 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs774963967 Functional Loss SNV dbSNP153 33..33 33 - - - 33388 RMVar_ID_33388 Human_SNP_ID_703509970 A-to-I Human chr22 + 37611965 37611961 37611965 TTTGAGGTCAGGAGTTTGAGACCAGCCTGACCAACATGGTGAAATTCCATCTCTACCAAAAATAC TTTGAGGTCAGGAGTTTGAGACCAGCCTG____ACATGGTGAAATTCCATCTCTACCAAAAATAC GACCA G GGA1 Ensembl:ENSG00000100083 Protein coding intron GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-Seq:(High) rs993716903 Functional Loss DEL dbSNP153 30..33 33 - - - 33389 RMVar_ID_33389 Human_SNP_ID_703509974 A-to-I Human chr22 + 37611968 37611968 37611968 GAGGTCAGGAGTTTGAGACCAGCCTGACCAACATGGTGAAATTCCATCTCTACCAAAAATACAAA GAGGTCAGGAGTTTGAGACCAGCCTGACCAACGTGGTGAAATTCCATCTCTACCAAAAATACAAA A G GGA1 Ensembl:ENSG00000100083 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs3207102 Functional Loss SNV dbSNP153 33..33 33 - - - 33390 RMVar_ID_33390 Human_SNP_ID_703509998 A-to-I Human chr22 + 37612049 37612049 37612049 GGTGGTGGACGCCTGTGATCCCAGCTACTCTCAGGAGGCTGAAGCAGGAGAATCGTTTGAACCCA GGTGGTGGACGCCTGTGATCCCAGCTACTCTCGGGAGGCTGAAGCAGGAGAATCGTTTGAACCCA A G GGA1 Ensembl:ENSG00000100083 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs3207109 Functional Loss SNV dbSNP153 33..33 33 - - - 33391 RMVar_ID_33391 Human_SNP_ID_703510002 A-to-I Human chr22 + 37612067 37612067 37612067 TCCCAGCTACTCTCAGGAGGCTGAAGCAGGAGAATCGTTTGAACCCAGGAAGCTGAGATTGCAGT TCCCAGCTACTCTCAGGAGGCTGAAGCAGGAGGATCGTTTGAACCCAGGAAGCTGAGATTGCAGT A G GGA1 Ensembl:ENSG00000100083 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1569196723 Functional Loss SNV dbSNP153 33..33 33 - - - 33392 RMVar_ID_33392 Human_SNP_ID_703510063 A-to-I Human chr22 + 37612203 37612203 37612203 TAAAAAAATACAGGCCGGACGCAGTGGCTCACACCTGTAATTCCAGTACTTTGGGAGGCCGAGGC TAAAAAAATACAGGCCGGACGCAGTGGCTCACGCCTGTAATTCCAGTACTTTGGGAGGCCGAGGC A G GGA1 Ensembl:ENSG00000100083 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229,31158229 RNA-Seq:(High) rs772563061 Functional Loss SNV dbSNP153 33..33 33 - - - 33393 RMVar_ID_33393 Human_SNP_ID_703510083 A-to-I Human chr22 + 37612261 37612261 37612261 CCGAGGCAGGTGGATCACGAGGTTAGGAGATCAAGACCATCCTGGCTAACACAGTGAAACCCCGT CCGAGGCAGGTGGATCACGAGGTTAGGAGATCGAGACCATCCTGGCTAACACAGTGAAACCCCGT A G GGA1 Ensembl:ENSG00000100083 Protein coding intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1294479268 Functional Loss SNV dbSNP153 33..33 33 - - - 33394 RMVar_ID_33394 Human_SNP_ID_703510089 A-to-I Human chr22 + 37612276 37612276 37612276 CACGAGGTTAGGAGATCAAGACCATCCTGGCTAACACAGTGAAACCCCGTCTCTACTAAAAATAC CACGAGGTTAGGAGATCAAGACCATCCTGGCTGACACAGTGAAACCCCGTCTCTACTAAAAATAC A G GGA1 Ensembl:ENSG00000100083 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1318661055 Functional Loss SNV dbSNP153 33..33 33 - - - 33395 RMVar_ID_33395 Human_SNP_ID_703510092 A-to-I Human chr22 + 37612281 37612281 37612281 GGTTAGGAGATCAAGACCATCCTGGCTAACACAGTGAAACCCCGTCTCTACTAAAAATACAAAAA GGTTAGGAGATCAAGACCATCCTGGCTAACACGGTGAAACCCCGTCTCTACTAAAAATACAAAAA A G GGA1 Ensembl:ENSG00000100083 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1358411917 Functional Loss SNV dbSNP153 33..33 33 - - - 33396 RMVar_ID_33396 Human_SNP_ID_703510292 A-to-I Human chr22 + 37612691 37612691 37612691 AGCTACTCGGGAGGCTGAGGAAGGAGAATGGCATGAACCTGGGAGGCGGAGCTTGCAGTGAGCCG AGCTACTCGGGAGGCTGAGGAAGGAGAATGGCGTGAACCTGGGAGGCGGAGCTTGCAGTGAGCCG A G GGA1 Ensembl:ENSG00000100083 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs575889379 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10380 33397 RMVar_ID_33397 Human_SNP_ID_703510320 A-to-I Human chr22 + 37612753 37612753 37612753 CCGAGATCGTGCCACTGCACTCCAGCCTGGGCAACAGCGTGAGACTCGTCTCAAAAAAAAAAAAA CCGAGATCGTGCCACTGCACTCCAGCCTGGGCGACAGCGTGAGACTCGTCTCAAAAAAAAAAAAA A G GGA1 Ensembl:ENSG00000100083 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs559864321 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25668745 33398 RMVar_ID_33398 Human_SNP_ID_703514551 A-to-I Human chr22 + 37627966 37627966 37627966 CTCCCATCTCAGGCTCCTGAGTAGTTGGGACTACAGGTGTGTGCCACCACACCCGGTTAATTAGT CTCCCATCTCAGGCTCCTGAGTAGTTGGGACTGCAGGTGTGTGCCACCACACCCGGTTAATTAGT A G GGA1 Ensembl:ENSG00000100083 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1411773494 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8893,RMVar_hsa_circ_375810,RMVar_hsa_circ_113618,RMVar_hsa_circ_214169,RMVar_hsa_circ_214168,RMVar_hsa_circ_125019,RMVar_hsa_circ_75698,RMVar_hsa_circ_214173,RMVar_hsa_circ_214178,RMVar_hsa_circ_82922,RMVar_hsa_circ_214177 33399 RMVar_ID_33399 Human_SNP_ID_703521493 A-to-I Human chr22 + 37651459 37651459 37651459 TCAAGCAATTCTCCTGCCTTAGCCTCCCGAATAGCTGTGACTTCAGGCGTGCACCACCATAGCCG TCAAGCAATTCTCCTGCCTTAGCCTCCCGAATGGCTGTGACTTCAGGCGTGCACCACCATAGCCG A G SH3BP1,Z83844.3 Ensembl:ENSG00000100092,Ensembl:ENSG00000285304 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1317471122 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_308965 33400 RMVar_ID_33400 Human_SNP_ID_703554610 A-to-I Human chr22 + 37762171 37762171 37762171 CTCACTGCAGCCTCGAACTCTAGGGCTCAAGCAGTCTTCCCACCTCAGCCTCCTGAGTAGGAACC CTCACTGCAGCCTCGAACTCTAGGGCTCAAGCTGTCTTCCCACCTCAGCCTCCTGAGTAGGAACC A T TRIOBP Ensembl:ENSG00000100106 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270150503 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 33401 RMVar_ID_33401 Human_SNP_ID_703568491 A-to-I Human chr22 + 37809591 37809591 37809591 CCTGAAATCGTAGCACTTTGGGAGGCCAAGGCAGGAGGATTGCTTGAGGCTAGGAGTTCGAGACC CCTGAAATCGTAGCACTTTGGGAGGCCAAGGCGGGAGGATTGCTTGAGGCTAGGAGTTCGAGACC A G GCAT Ensembl:ENSG00000100116 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1315859607 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101795,RMVar_hsa_circ_214213 33402 RMVar_ID_33402 Human_SNP_ID_703576171 A-to-I Human chr22 - 37835180 37835180 37835180 TTTTTTATTTTTAGTAGAGATGGGATTTCACCATGTTGGTCAGGCTGGTCTCGAACTCCTGACCT TTTTTTATTTTTAGTAGAGATGGGATTTCACCGTGTTGGTCAGGCTGGTCTCGAACTCCTGACCT T C ANKRD54 Ensembl:ENSG00000100124 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1325117924 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119022,RMVar_hsa_circ_81722,RMVar_hsa_circ_214220,RMVar_hsa_circ_214221,RMVar_hsa_circ_350018 33403 RMVar_ID_33403 Human_SNP_ID_703580083 A-to-I Human chr22 - 37848547 37848547 37848547 TATTAAAAATACAAAAATTAGCCGGGAGTGGTAGCGTCCGCCTGTAATCCCAGCTACTCAGGAGG TATTAAAAATACAAAAATTAGCCGGGAGTGGTGGCGTCCGCCTGTAATCCCAGCTACTCAGGAGG T C ANKRD54 Ensembl:ENSG00000100124 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs769272617 Functional Loss SNV dbSNP153 33..33 33 - - - 33404 RMVar_ID_33404 Human_SNP_ID_703580106 A-to-I Human chr22 - 37848623 37848623 37848623 GGGAGGCCGAGGCGGGTGGATGATCTGAGATCAGGAGTTCGAGACCAGCCTGGCCGAAATGGCGA GGGAGGCCGAGGCGGGTGGATGATCTGAGATCGGGAGTTCGAGACCAGCCTGGCCGAAATGGCGA T C ANKRD54 Ensembl:ENSG00000100124 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1191762264 Functional Loss SNV dbSNP153 33..33 33 - - - 33405 RMVar_ID_33405 Human_SNP_ID_703582306 A-to-I Human chr22 + 37856151 37856151 37856151 ACAATCTTGGCTCACTGCAACCTCCGCCTCCCAGGTTCAAGCGATTCTCCTAGGTTCAAGCAATT ACAATCTTGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGCGATTCTCCTAGGTTCAAGCAATT A G EIF3L Ensembl:ENSG00000100129 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1331047373 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14478664 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_57498,RMVar_hsa_circ_214232,RMVar_hsa_circ_80278,RMVar_hsa_circ_302466,RMVar_hsa_circ_11878 33406 RMVar_ID_33406 Human_SNP_ID_703582342 A-to-I Human chr22 + 37856242 37856242 37856242 GGGATTACAGGCGCCCGCCACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCA GGGATTACAGGCGCCCGCCACCACGCCCAGCTGATTTTTGTATTTTTAGTAGAGACGGGGTTTCA A G EIF3L Ensembl:ENSG00000100129 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1224018871 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_57498,RMVar_hsa_circ_214232,RMVar_hsa_circ_80278,RMVar_hsa_circ_302466,RMVar_hsa_circ_11878 33407 RMVar_ID_33407 Human_SNP_ID_703582364 A-to-I Human chr22 + 37856311 37856311 37856311 GTTGGCCAGGCTGGTCTCGAACTGCTGACGTCAGGTGATTCGCCCACCTCAGCCTCCCAAAGTGC GTTGGCCAGGCTGGTCTCGAACTGCTGACGTCGGGTGATTCGCCCACCTCAGCCTCCCAAAGTGC A G EIF3L Ensembl:ENSG00000100129 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1423038724 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7080327 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_57498,RMVar_hsa_circ_214232,RMVar_hsa_circ_80278,RMVar_hsa_circ_302466,RMVar_hsa_circ_11878 33408 RMVar_ID_33408 Human_SNP_ID_703582398 A-to-I Human chr22 + 37856457 37856457 37856457 GTTGACCTGGCTGATCTTGAACTCCTGACCTCAAGTGATCTTCCCAGAGTGCTGAGATTACAGGC GTTGACCTGGCTGATCTTGAACTCCTGACCTCGAGTGATCTTCCCAGAGTGCTGAGATTACAGGC A G EIF3L Ensembl:ENSG00000100129 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1302457730 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14478666,Human_RBP_ID_17572697 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_57498,RMVar_hsa_circ_214232,RMVar_hsa_circ_80278,RMVar_hsa_circ_302466,RMVar_hsa_circ_11878 33409 RMVar_ID_33409 Human_SNP_ID_703582454 A-to-I Human chr22 + 37856680 37856680 37856680 CAGCCTGATTAACGTGGAGAAACCCCATCTCTACTAAAAATACAAAATCAGCCGGGCATGGTGAC CAGCCTGATTAACGTGGAGAAACCCCATCTCTTCTAAAAATACAAAATCAGCCGGGCATGGTGAC A T EIF3L Ensembl:ENSG00000100129 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs993595940 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_57498,RMVar_hsa_circ_214232,RMVar_hsa_circ_80278,RMVar_hsa_circ_302466,RMVar_hsa_circ_11878 33410 RMVar_ID_33410 Human_SNP_ID_703582485 A-to-I Human chr22 + 37856759 37856759 37856759 CCAGCTACTTGGGAGGTGGAGGCAGGAGAATCACTTGAACCCGGAAGGCAGAGGTTGCGGTGAGC CCAGCTACTTGGGAGGTGGAGGCAGGAGAATCGCTTGAACCCGGAAGGCAGAGGTTGCGGTGAGC A G EIF3L Ensembl:ENSG00000100129 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1445622984 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_57498,RMVar_hsa_circ_214232,RMVar_hsa_circ_80278,RMVar_hsa_circ_302466,RMVar_hsa_circ_11878 33411 RMVar_ID_33411 Human_SNP_ID_703582609 A-to-I Human chr22 + 37857176 37857176 37857176 GAGGTCAGGAGATCGAGACCATCCTGGCTAACACGGTGAAACCCCGTCTCTACTAAAAATGCAAA GAGGTCAGGAGATCGAGACCATCCTGGCTAACGCGGTGAAACCCCGTCTCTACTAAAAATGCAAA A G EIF3L Ensembl:ENSG00000100129 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1172119728 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_57498,RMVar_hsa_circ_214232,RMVar_hsa_circ_80278,RMVar_hsa_circ_302466,RMVar_hsa_circ_11878 33412 RMVar_ID_33412 Human_SNP_ID_703582610 A-to-I Human chr22 + 37857176 37857176 37857176 GAGGTCAGGAGATCGAGACCATCCTGGCTAACACGGTGAAACCCCGTCTCTACTAAAAATGCAAA GAGGTCAGGAGATCGAGACCATCCTGGCTAACTCGGTGAAACCCCGTCTCTACTAAAAATGCAAA A T EIF3L Ensembl:ENSG00000100129 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1172119728 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_57498,RMVar_hsa_circ_214232,RMVar_hsa_circ_80278,RMVar_hsa_circ_302466,RMVar_hsa_circ_11878 33413 RMVar_ID_33413 Human_SNP_ID_703582637 A-to-I Human chr22 + 37857259 37857259 37857259 CGGCATGGTGGCGGGCACCTGTAGTCCCAGCTACTCGGGAGGCTGAGACAGGAGAATGGCGTGAA CGGCATGGTGGCGGGCACCTGTAGTCCCAGCTTCTCGGGAGGCTGAGACAGGAGAATGGCGTGAA A T EIF3L Ensembl:ENSG00000100129 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs568117354 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_57498,RMVar_hsa_circ_214232,RMVar_hsa_circ_80278,RMVar_hsa_circ_302466,RMVar_hsa_circ_11878 33414 RMVar_ID_33414 Human_SNP_ID_703582810 A-to-I Human chr22 + 37857648 37857648 37857648 CTCGCTGCAACCTCTGCCTCCTGGGCTCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGG CTCGCTGCAACCTCTGCCTCCTGGGCTCAAGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGG A C EIF3L Ensembl:ENSG00000100129 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs57323429 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_57498,RMVar_hsa_circ_214232,RMVar_hsa_circ_80278,RMVar_hsa_circ_302466,RMVar_hsa_circ_11878 33415 RMVar_ID_33415 Human_SNP_ID_703582814 A-to-I Human chr22 + 37857662 37857662 37857662 TGCCTCCTGGGCTCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCACCTG TGCCTCCTGGGCTCAAGCAATTCTCCTGCCTCGGCCTCCCGAGTAGCTGGGATTACAGGCACCTG A G EIF3L Ensembl:ENSG00000100129 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs964815813 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_57498,RMVar_hsa_circ_214232,RMVar_hsa_circ_80278,RMVar_hsa_circ_302466,RMVar_hsa_circ_11878 33416 RMVar_ID_33416 Human_SNP_ID_703582818 A-to-I Human chr22 + 37857674 37857674 37857674 TCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCACCTGGCGGATTTTTTG TCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTGGCTGGGATTACAGGCACCTGGCGGATTTTTTG A G EIF3L Ensembl:ENSG00000100129 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs938756077 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_57498,RMVar_hsa_circ_214232,RMVar_hsa_circ_80278,RMVar_hsa_circ_302466,RMVar_hsa_circ_11878 33417 RMVar_ID_33417 Human_SNP_ID_703582826 A-to-I Human chr22 + 37857714 37857714 37857714 TTACAGGCACCTGGCGGATTTTTTGTATTTTTAGTAGAGATGGTGTTTCACCATCTTGGCCAGGC TTACAGGCACCTGGCGGATTTTTTGTATTTTTGGTAGAGATGGTGTTTCACCATCTTGGCCAGGC A G EIF3L Ensembl:ENSG00000100129 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1241853907 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25669000 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_57498,RMVar_hsa_circ_214232,RMVar_hsa_circ_80278,RMVar_hsa_circ_302466,RMVar_hsa_circ_11878 33418 RMVar_ID_33418 Human_SNP_ID_703582870 A-to-I Human chr22 + 37857914 37857914 37857914 TTCTGTGGCTGGGTGTCGTAGCTCACGGCTGTAATTCTGGTACTTTGGGAAGCTGAGGTGGGAGG TTCTGTGGCTGGGTGTCGTAGCTCACGGCTGTGATTCTGGTACTTTGGGAAGCTGAGGTGGGAGG A G EIF3L Ensembl:ENSG00000100129 Protein coding intron GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-Seq:(High) rs907982947 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_57498,RMVar_hsa_circ_214232,RMVar_hsa_circ_80278,RMVar_hsa_circ_302466,RMVar_hsa_circ_11878 33419 RMVar_ID_33419 Human_SNP_ID_703582916 A-to-I Human chr22 + 37858091 37858091 37858091 CCACCTACTCGGGAGGCTGAGGTGGAAGGATCACTTGAGCCCTGGAAGTCGAGGCTGCAGTGAGC CCACCTACTCGGGAGGCTGAGGTGGAAGGATCCCTTGAGCCCTGGAAGTCGAGGCTGCAGTGAGC A C EIF3L Ensembl:ENSG00000100129 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886392871 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_57498,RMVar_hsa_circ_214232,RMVar_hsa_circ_80278,RMVar_hsa_circ_302466,RMVar_hsa_circ_11878 33420 RMVar_ID_33420 Human_SNP_ID_703582917 A-to-I Human chr22 + 37858091 37858091 37858091 CCACCTACTCGGGAGGCTGAGGTGGAAGGATCACTTGAGCCCTGGAAGTCGAGGCTGCAGTGAGC CCACCTACTCGGGAGGCTGAGGTGGAAGGATCGCTTGAGCCCTGGAAGTCGAGGCTGCAGTGAGC A G EIF3L Ensembl:ENSG00000100129 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886392871 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_57498,RMVar_hsa_circ_214232,RMVar_hsa_circ_80278,RMVar_hsa_circ_302466,RMVar_hsa_circ_11878 33421 RMVar_ID_33421 Human_SNP_ID_703583021 A-to-I Human chr22 + 37858304 37858304 37858304 TGCTGGAGTGTAGTGTGATAATGGCTGACTGCAACCTGTGCCTGCTGGGCTCAAGCGATCCTCCC TGCTGGAGTGTAGTGTGATAATGGCTGACTGCCACCTGTGCCTGCTGGGCTCAAGCGATCCTCCC A C EIF3L Ensembl:ENSG00000100129 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1408270804 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7080344,Human_RBP_ID_14478704 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_57498,RMVar_hsa_circ_214232,RMVar_hsa_circ_80278,RMVar_hsa_circ_302466,RMVar_hsa_circ_11878 33422 RMVar_ID_33422 Human_SNP_ID_703584741 A-to-I Human chr22 + 37864093 37864089 37864093 CTCAAAAAAAAAAAAGAAAGAGTCAGGGTCTCACTCTGTTGCTCAGGCTAGAGTGCAGTGATAAT CTCAAAAAAAAAAAAGAAAGAGTCAGGGT____CTCTGTTGCTCAGGCTAGAGTGCAGTGATAAT TCTCA T EIF3L Ensembl:ENSG00000100129 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs746404971 Functional Loss DEL dbSNP153 30..33 33 - - - 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_214237,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_214238 33423 RMVar_ID_33423 Human_SNP_ID_703584758 A-to-I Human chr22 + 37864169 37864169 37864169 GCCTAGAACTCCTGGGTTCAAGTGATTTTCCCACCTCAGCCACCTGAGTAGCTGCCACTACAAGG GCCTAGAACTCCTGGGTTCAAGTGATTTTCCCCCCTCAGCCACCTGAGTAGCTGCCACTACAAGG A C EIF3L Ensembl:ENSG00000100129 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928478591 Functional Loss SNV dbSNP153 33..33 33 - - - 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_214237,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_214238 33424 RMVar_ID_33424 Human_SNP_ID_703584759 A-to-I Human chr22 + 37864169 37864169 37864169 GCCTAGAACTCCTGGGTTCAAGTGATTTTCCCACCTCAGCCACCTGAGTAGCTGCCACTACAAGG GCCTAGAACTCCTGGGTTCAAGTGATTTTCCCGCCTCAGCCACCTGAGTAGCTGCCACTACAAGG A G EIF3L Ensembl:ENSG00000100129 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928478591 Functional Loss SNV dbSNP153 33..33 33 - - - 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_214237,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_214238 33425 RMVar_ID_33425 Human_SNP_ID_703584905 A-to-I Human chr22 + 37864722 37864712 37864723 CACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCTCCATGTTGACCAGGCTGG CACCACGCCCAGCTAATTTTTGT___________AGACGGGGTTTCTCCATGTTGACCAGGCTGG TATTTTTAGTAG T EIF3L Ensembl:ENSG00000100129 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1277906070 Functional Loss DEL dbSNP153 24..34 33 - - - 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_214237,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_214238 33426 RMVar_ID_33426 Human_SNP_ID_703585553 A-to-I Human chr22 + 37867074 37867074 37867074 TTCTTTGTTTAAGAGATGGGGGTCTTGCCTTTATGGTCCAGGCTGGAGTGCAGTGGTGTGATCAT TTCTTTGTTTAAGAGATGGGGGTCTTGCCTTTGTGGTCCAGGCTGGAGTGCAGTGGTGTGATCAT A G EIF3L Ensembl:ENSG00000100129 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1321130166 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7080393 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_214237,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_214238 33427 RMVar_ID_33427 Human_SNP_ID_703585668 A-to-I Human chr22 + 37867573 37867573 37867573 CCCAGCTACTCAGCAGCTGAGGGATGAGAATCACTTGAACCGAGAGGCAGAGGTTGCAGTGAGCT CCCAGCTACTCAGCAGCTGAGGGATGAGAATCGCTTGAACCGAGAGGCAGAGGTTGCAGTGAGCT A G EIF3L Ensembl:ENSG00000100129 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017570926 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14479021 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_214237,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_214238 33428 RMVar_ID_33428 Human_SNP_ID_703585763 A-to-I Human chr22 + 37867875 37867869 37867876 TACTCAGGAGGCTGAGGCAGGAGAATGGCGTGAACCCAGGAGGCGGAGCTTGCAGAGAGCCGAGA TACTCAGGAGGCTGAGGCAGGAGAATG_______CCCAGGAGGCGGAGCTTGCAGAGAGCCGAGA GGCGTGAA G EIF3L Ensembl:ENSG00000100129 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1485480744 Functional Loss DEL dbSNP153 28..34 33 - - - 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_214237,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_214238 33429 RMVar_ID_33429 Human_SNP_ID_703586183 A-to-I Human chr22 + 37868916 37868916 37868916 CGCCTGCATCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCACCCGGCCTGTTTTT CGCCTGCATCGGCCTCCCAAAGTGCTGGGATTGCAGGCATGAGCCACCGCACCCGGCCTGTTTTT A G EIF3L Ensembl:ENSG00000100129 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs776780252 Functional Loss SNV dbSNP153 33..33 33 - - - 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_214237,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_214238 33430 RMVar_ID_33430 Human_SNP_ID_703586216 A-to-I Human chr22 + 37869011 37869011 37869011 GTTGGCCAAGCTGTTCTCGAACTCTTGATCTCATGATCCATCCACCTTGGCTTCCCAAAGTGCTG GTTGGCCAAGCTGTTCTCGAACTCTTGATCTCGTGATCCATCCACCTTGGCTTCCCAAAGTGCTG A G EIF3L Ensembl:ENSG00000100129 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs911978436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14479042,Human_RBP_ID_25669077 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_214237,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_214238 33431 RMVar_ID_33431 Human_SNP_ID_703586260 A-to-I Human chr22 + 37869198 37869198 37869198 TCACTCACACTGGAATGCAGTGGCACAACCTCACCTCACTGTAGCCTCCGCCTCCTGGGCTCAGG TCACTCACACTGGAATGCAGTGGCACAACCTCGCCTCACTGTAGCCTCCGCCTCCTGGGCTCAGG A G EIF3L Ensembl:ENSG00000100129 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1467697995 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14479047 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_214237,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_214238 33432 RMVar_ID_33432 Human_SNP_ID_703586295 A-to-I Human chr22 + 37869331 37869331 37869331 GTTTGTGTTTTTTATAGCGATAGGGTTTTGCCATGTTTCCCAGGCTGGTCTTGAGCTCCTGGACC GTTTGTGTTTTTTATAGCGATAGGGTTTTGCCGTGTTTCCCAGGCTGGTCTTGAGCTCCTGGACC A G EIF3L Ensembl:ENSG00000100129 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs188722004 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14479053 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_214237,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_214238 33433 RMVar_ID_33433 Human_SNP_ID_703586724 A-to-I Human chr22 + 37871085 37871085 37871085 AGGAAGCAAAGATTGCAGTGAACTGAGATCACACCACTGTACTCTAGCCTGGGCCACAGAGCGAG AGGAAGCAAAGATTGCAGTGAACTGAGATCACGCCACTGTACTCTAGCCTGGGCCACAGAGCGAG A G EIF3L Ensembl:ENSG00000100129 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965701329 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10057545,Human_RBP_ID_14479135,Human_RBP_ID_25682416 RMVar_hsa_circ_11140,RMVar_hsa_circ_78368,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_214232,RMVar_hsa_circ_80278,RMVar_hsa_circ_360797,RMVar_hsa_circ_362019,RMVar_hsa_circ_80513,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 33434 RMVar_ID_33434 Human_SNP_ID_703586725 A-to-I Human chr22 + 37871085 37871085 37871085 AGGAAGCAAAGATTGCAGTGAACTGAGATCACACCACTGTACTCTAGCCTGGGCCACAGAGCGAG AGGAAGCAAAGATTGCAGTGAACTGAGATCACTCCACTGTACTCTAGCCTGGGCCACAGAGCGAG A T EIF3L Ensembl:ENSG00000100129 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965701329 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10057545,Human_RBP_ID_14479135,Human_RBP_ID_25682416 RMVar_hsa_circ_11140,RMVar_hsa_circ_78368,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_214232,RMVar_hsa_circ_80278,RMVar_hsa_circ_360797,RMVar_hsa_circ_362019,RMVar_hsa_circ_80513,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 33435 RMVar_ID_33435 Human_SNP_ID_703586923 A-to-I Human chr22 + 37871826 37871826 37871826 GGGAGGCAGAGGTTGCAGTGAGCCGAGATCGCACCACTGCACTACAGTCTTAGTGACAGAGCGAG GGGAGGCAGAGGTTGCAGTGAGCCGAGATCGCGCCACTGCACTACAGTCTTAGTGACAGAGCGAG A G EIF3L Ensembl:ENSG00000100129 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs565856388 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11140,RMVar_hsa_circ_78368,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_214232,RMVar_hsa_circ_80278,RMVar_hsa_circ_360797,RMVar_hsa_circ_362019,RMVar_hsa_circ_80513,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 33436 RMVar_ID_33436 Human_SNP_ID_703587060 A-to-I Human chr22 + 37872217 37872217 37872217 TCAGTTCACTGCATCCTCTGCCTCCGGGGTTCAAGCGATTCTCCTGTCTCAGCCTCCAGGGATAT TCAGTTCACTGCATCCTCTGCCTCCGGGGTTCGAGCGATTCTCCTGTCTCAGCCTCCAGGGATAT A G EIF3L Ensembl:ENSG00000100129 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1030117495 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11140,RMVar_hsa_circ_78368,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_214232,RMVar_hsa_circ_80278,RMVar_hsa_circ_360797,RMVar_hsa_circ_362019,RMVar_hsa_circ_80513,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 33437 RMVar_ID_33437 Human_SNP_ID_703587085 A-to-I Human chr22 + 37872305 37872305 37872305 CGCCACCACGCCGGGCTGATTTTTGTATTTTTAGTAGAACAGAGTTTGACCATGTTGGCCAGGCT CGCCACCACGCCGGGCTGATTTTTGTATTTTTTGTAGAACAGAGTTTGACCATGTTGGCCAGGCT A T EIF3L Ensembl:ENSG00000100129 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1339330079 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14479187 RMVar_hsa_circ_11140,RMVar_hsa_circ_78368,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_214232,RMVar_hsa_circ_80278,RMVar_hsa_circ_360797,RMVar_hsa_circ_362019,RMVar_hsa_circ_80513,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 33438 RMVar_ID_33438 Human_SNP_ID_703587097 A-to-I Human chr22 + 37872358 37872358 37872358 GTTGGCCAGGCTGCTCTTGAACTCCCGAGCTCAAGTGATCTGCCTGCCTCGGCCTCCCAAAGTGC GTTGGCCAGGCTGCTCTTGAACTCCCGAGCTCTAGTGATCTGCCTGCCTCGGCCTCCCAAAGTGC A T EIF3L Ensembl:ENSG00000100129 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1190562166 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14479187 RMVar_hsa_circ_11140,RMVar_hsa_circ_78368,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_214232,RMVar_hsa_circ_80278,RMVar_hsa_circ_360797,RMVar_hsa_circ_362019,RMVar_hsa_circ_80513,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 33439 RMVar_ID_33439 Human_SNP_ID_703587256 A-to-I Human chr22 + 37872992 37872986 37872992 GAAAATGTCTGCCCTTTTTTCCTTCTTTTTTTATTTTTATTTTTTTTGAGACAGAGTCTTGCTCT GAAAATGTCTGCCCTTTTTTCCTTCTT______TTTTTATTTTTTTTGAGACAGAGTCTTGCTCT TTTTTTA T EIF3L Ensembl:ENSG00000100129 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1293454496 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_14479225 RMVar_hsa_circ_11140,RMVar_hsa_circ_78368,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_214232,RMVar_hsa_circ_80278,RMVar_hsa_circ_360797,RMVar_hsa_circ_362019,RMVar_hsa_circ_80513,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 33440 RMVar_ID_33440 Human_SNP_ID_703587312 A-to-I Human chr22 + 37873209 37873209 37873209 CGGGGCTTCACCATGTTGGGCAGGCTGGGCTCAAACTCCTGACCTCAAGTGATACGTCCGCCTCG CGGGGCTTCACCATGTTGGGCAGGCTGGGCTCGAACTCCTGACCTCAAGTGATACGTCCGCCTCG A G EIF3L Ensembl:ENSG00000100129 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs548045588 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14479228 RMVar_hsa_circ_11140,RMVar_hsa_circ_78368,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_214232,RMVar_hsa_circ_80278,RMVar_hsa_circ_360797,RMVar_hsa_circ_362019,RMVar_hsa_circ_80513,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 33441 RMVar_ID_33441 Human_SNP_ID_703587401 A-to-I Human chr22 + 37873424 37873424 37873424 GGGTTCATGCCATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGCTACAGGCGCCCACCACCATGC GGGTTCATGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGCTACAGGCGCCCACCACCATGC A G EIF3L Ensembl:ENSG00000100129 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs113480725 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11140,RMVar_hsa_circ_78368,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_214232,RMVar_hsa_circ_80278,RMVar_hsa_circ_360797,RMVar_hsa_circ_362019,RMVar_hsa_circ_80513,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 33442 RMVar_ID_33442 Human_SNP_ID_703587403 A-to-I Human chr22 + 37873428 37873428 37873428 TCATGCCATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGCTACAGGCGCCCACCACCATGCCCGG TCATGCCATTCTCCTGCCTCAGCCTCCCAAGTGGCTGGGCTACAGGCGCCCACCACCATGCCCGG A G EIF3L Ensembl:ENSG00000100129 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1014621029 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11140,RMVar_hsa_circ_78368,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_214232,RMVar_hsa_circ_80278,RMVar_hsa_circ_360797,RMVar_hsa_circ_362019,RMVar_hsa_circ_80513,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 33443 RMVar_ID_33443 Human_SNP_ID_703589063 A-to-I Human chr22 + 37879043 37879043 37879043 TCGGCTCCCTGCAACCTCCGCCTCCCAGGTTCAAGCAATTCTCCTGCCTCAGCATCCTGAGTAGC TCGGCTCCCTGCAACCTCCGCCTCCCAGGTTCCAGCAATTCTCCTGCCTCAGCATCCTGAGTAGC A C AL022311.1,EIF3L Ensembl:ENSG00000279738,Ensembl:ENSG00000100129 lincRNA,Protein coding exon,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1229635646 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25643,RMVar_hsa_circ_8617,RMVar_hsa_circ_214245,RMVar_hsa_circ_104430 33444 RMVar_ID_33444 Human_SNP_ID_703589082 A-to-I Human chr22 + 37879124 37879107 37879125 CGCCACCACACCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTTGCCATGTTGGCCAGGC CGCCACCACACCTGGC__________________TAGAGACAGGGTTTTGCCATGTTGGCCAGGC CTAATTTTTGTATTTTTAG C AL022311.1,EIF3L Ensembl:ENSG00000279738,Ensembl:ENSG00000100129 lincRNA,Protein coding exon,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1270758587 Functional Loss DEL dbSNP153 17..34 33 - - - RMVar_hsa_circ_25643,RMVar_hsa_circ_8617,RMVar_hsa_circ_214245,RMVar_hsa_circ_104430 33445 RMVar_ID_33445 Human_SNP_ID_703589121 A-to-I Human chr22 + 37879289 37879289 37879289 TTGGGAGGCCGAGATGGACAGATCATGGGGTCAAGAGATCAAGACCATCCTAGCCAACATGGTGA TTGGGAGGCCGAGATGGACAGATCATGGGGTCGAGAGATCAAGACCATCCTAGCCAACATGGTGA A G AL022311.1,EIF3L Ensembl:ENSG00000279738,Ensembl:ENSG00000100129 lincRNA,Protein coding exon,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1268918871 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25643,RMVar_hsa_circ_8617,RMVar_hsa_circ_214245,RMVar_hsa_circ_104430 33446 RMVar_ID_33446 Human_SNP_ID_703589138 A-to-I Human chr22 + 37879380 37879380 37879380 AGCTGGGCATGGTGGCGCATACCTGTAGTCCCAGCTACCCGGGAGGCTGAGGCAGGAGAATCACT AGCTGGGCATGGTGGCGCATACCTGTAGTCCCCGCTACCCGGGAGGCTGAGGCAGGAGAATCACT A C AL022311.1,EIF3L Ensembl:ENSG00000279738,Ensembl:ENSG00000100129 lincRNA,Protein coding exon,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1030127739 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25643,RMVar_hsa_circ_8617,RMVar_hsa_circ_214245,RMVar_hsa_circ_104430 33447 RMVar_ID_33447 Human_SNP_ID_703589288 A-to-I Human chr22 + 37879939 37879939 37879939 CTCTTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCTCACACCACCACACCCAGCTAATATTT CTCTTGCCTCAGCCTCCTGAGTAGCTGGGATTGCAGGCTCACACCACCACACCCAGCTAATATTT A G AL022311.1,EIF3L Ensembl:ENSG00000279738,Ensembl:ENSG00000100129 lincRNA,Protein coding exon,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1569123246 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25643,RMVar_hsa_circ_8617,RMVar_hsa_circ_214245,RMVar_hsa_circ_104430 33448 RMVar_ID_33448 Human_SNP_ID_703589327 A-to-I Human chr22 + 37880069 37880069 37880069 GTGATCCGCCCGCCTCGGCCTCCCAGAGTGCTAGGATTACAGGCGTGAGCCATCGCGCCCGGTAT GTGATCCGCCCGCCTCGGCCTCCCAGAGTGCTGGGATTACAGGCGTGAGCCATCGCGCCCGGTAT A G AL022311.1,EIF3L Ensembl:ENSG00000279738,Ensembl:ENSG00000100129 lincRNA,Protein coding exon,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1370818826 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25643,RMVar_hsa_circ_8617,RMVar_hsa_circ_214245,RMVar_hsa_circ_104430 33449 RMVar_ID_33449 Human_SNP_ID_703589745 A-to-I Human chr22 + 37881670 37881670 37881670 CCCTCAGGTGATCTGCCCGCCTCGGCCTCCCAAAGTGCTGGGGTTACAGACATGAGCCACCACAC CCCTCAGGTGATCTGCCCGCCTCGGCCTCCCAGAGTGCTGGGGTTACAGACATGAGCCACCACAC A G AL022311.1,EIF3L Ensembl:ENSG00000279738,Ensembl:ENSG00000100129 lincRNA,Protein coding exon,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs921035767 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25643,RMVar_hsa_circ_8617,RMVar_hsa_circ_214245,RMVar_hsa_circ_104430 33450 RMVar_ID_33450 Human_SNP_ID_703589894 A-to-I Human chr22 + 37882192 37882192 37882192 AGCCAGGCATGGTGGCACATGCCTGTAATCCCAGTAACTTGGGAGGCTGAGACAGGAGACTCACT AGCCAGGCATGGTGGCACATGCCTGTAATCCCGGTAACTTGGGAGGCTGAGACAGGAGACTCACT A G AL022311.1,EIF3L Ensembl:ENSG00000279738,Ensembl:ENSG00000100129 lincRNA,Protein coding exon,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1265023954 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25643,RMVar_hsa_circ_8617,RMVar_hsa_circ_214245,RMVar_hsa_circ_104430 33451 RMVar_ID_33451 Human_SNP_ID_703590098 A-to-I Human chr22 + 37882944 37882944 37882944 CTTGCTTGAACCTAGGAGGCGGAGGTTGCAGTAAGCCAAGATTGCACCACTGCACTCCAGCCTGG CTTGCTTGAACCTAGGAGGCGGAGGTTGCAGTGAGCCAAGATTGCACCACTGCACTCCAGCCTGG A G AL022311.1,EIF3L Ensembl:ENSG00000279738,Ensembl:ENSG00000100129 lincRNA,Protein coding exon,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1198860147 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25643,RMVar_hsa_circ_8617,RMVar_hsa_circ_214245,RMVar_hsa_circ_104430 33452 RMVar_ID_33452 Human_SNP_ID_703590664 A-to-I Human chr22 + 37885044 37885044 37885044 GGGCTCAGGTGATCCTCCTATCTCAGCTTCTCAAGTAGCTGGGACTACAGGACTGCACCACCACA GGGCTCAGGTGATCCTCCTATCTCAGCTTCTCGAGTAGCTGGGACTACAGGACTGCACCACCACA A G AL022311.1,EIF3L Ensembl:ENSG00000279738,Ensembl:ENSG00000100129 lincRNA,Protein coding exon,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs992662639 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14479479 RMVar_hsa_circ_25643,RMVar_hsa_circ_8617,RMVar_hsa_circ_214245,RMVar_hsa_circ_104430 33453 RMVar_ID_33453 Human_SNP_ID_703590681 A-to-I Human chr22 + 37885102 37885102 37885102 CACCACATCTTGCTAATTTTTGTATTTTTTGTAGAGATGGGGTTTTACCATGTTGCCCAGCCTGG CACCACATCTTGCTAATTTTTGTATTTTTTGTGGAGATGGGGTTTTACCATGTTGCCCAGCCTGG A G AL022311.1,EIF3L Ensembl:ENSG00000279738,Ensembl:ENSG00000100129 lincRNA,Protein coding exon,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs917231763 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25643,RMVar_hsa_circ_8617,RMVar_hsa_circ_214245,RMVar_hsa_circ_104430 33454 RMVar_ID_33454 Human_SNP_ID_703590846 A-to-I Human chr22 + 37885765 37885765 37885765 TCCTGGGATTACAGGTGCCCGCCACTACGCCCAGCTAATTTTTAGTAGAGATGGGGTTTCACCAT TCCTGGGATTACAGGTGCCCGCCACTACGCCCTGCTAATTTTTAGTAGAGATGGGGTTTCACCAT A T AL022311.1,EIF3L Ensembl:ENSG00000279738,Ensembl:ENSG00000100129 lincRNA,Protein coding exon,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs985501701 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25643,RMVar_hsa_circ_8617,RMVar_hsa_circ_214245,RMVar_hsa_circ_104430 33455 RMVar_ID_33455 Human_SNP_ID_703590869 A-to-I Human chr22 + 37885846 37885846 37885846 TTGAATTCCCAACCTCCCAAAGTGCTGGGATTACAGGCGTGAGTCACCATGCCCAGCCAGCATAA TTGAATTCCCAACCTCCCAAAGTGCTGGGATTGCAGGCGTGAGTCACCATGCCCAGCCAGCATAA A G AL022311.1,EIF3L Ensembl:ENSG00000279738,Ensembl:ENSG00000100129 lincRNA,Protein coding exon,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1464773238 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25643,RMVar_hsa_circ_8617,RMVar_hsa_circ_214245,RMVar_hsa_circ_104430 33456 RMVar_ID_33456 Human_SNP_ID_703591847 A-to-I Human chr22 + 37889316 37889316 37889316 CTCGTGATCTGCCCATCTCTGCCTCCTAAAGTACTGGGATTACAGGCGTGAGCCACCGTGCCCAG CTCGTGATCTGCCCATCTCTGCCTCCTAAAGTGCTGGGATTACAGGCGTGAGCCACCGTGCCCAG A G AL022311.1,EIF3L Ensembl:ENSG00000279738,Ensembl:ENSG00000100129 lincRNA,Protein coding exon,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1257493403 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14479575 33457 RMVar_ID_33457 Human_SNP_ID_703604970 A-to-I Human chr22 + 37938557 37938557 37938557 CTTACTGCAATCTCTGCCTCCTAGGTTCAAGCAATTCTCCTGTCTCAGCCTCCTGAGTTGCTGGG CTTACTGCAATCTCTGCCTCCTAGGTTCAAGCGATTCTCCTGTCTCAGCCTCCTGAGTTGCTGGG A G MICALL1 Ensembl:ENSG00000100139 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs998015839 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120352,RMVar_hsa_circ_214248 33458 RMVar_ID_33458 Human_SNP_ID_703606529 A-to-I Human chr22 + 37944743 37944743 37944743 CAACATGGTGAAACCCCGTGTCTACTAAAAATACAAAAATTAGCCAGGCATGGTGGCGGGCGCTG CAACATGGTGAAACCCCGTGTCTACTAAAAATGCAAAAATTAGCCAGGCATGGTGGCGGGCGCTG A G AL031587.5 Ensembl:ENSG00000278948 Other exon GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1231873892 Functional Loss SNV dbSNP153 33..33 33 - - - 33459 RMVar_ID_33459 Human_SNP_ID_703606550 A-to-I Human chr22 + 37944788 37944788 37944788 AGGCATGGTGGCGGGCGCTGGTAATCCCAGCTACTCAGGTGGCTGAGGCAGGAGGGATTGCTTGA AGGCATGGTGGCGGGCGCTGGTAATCCCAGCTGCTCAGGTGGCTGAGGCAGGAGGGATTGCTTGA A G AL031587.5 Ensembl:ENSG00000278948 Other exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1237482196 Functional Loss SNV dbSNP153 33..33 33 - - - 33460 RMVar_ID_33460 Human_SNP_ID_703606810 A-to-I Human chr22 + 37945588 37945588 37945588 ACAATTTCGGCTCACTGCAACCTCTCGGGCTCAAGTCATCCTCCCACCTCAGCCTCCCGAGTAGC ACAATTTCGGCTCACTGCAACCTCTCGGGCTCCAGTCATCCTCCCACCTCAGCCTCCCGAGTAGC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1308542624 Functional Loss SNV dbSNP153 33..33 33 - - - 33461 RMVar_ID_33461 Human_SNP_ID_703606812 A-to-I Human chr22 + 37945601 37945601 37945601 ACTGCAACCTCTCGGGCTCAAGTCATCCTCCCACCTCAGCCTCCCGAGTAGCTGGGACTACAGGT ACTGCAACCTCTCGGGCTCAAGTCATCCTCCCCCCTCAGCCTCCCGAGTAGCTGGGACTACAGGT A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs977000311 Functional Loss SNV dbSNP153 33..33 33 - - - 33462 RMVar_ID_33462 Human_SNP_ID_703607513 A-to-I Human chr22 + 37947843 37947843 37947843 TAAAAATAAAAGTTGGCCGGGCATGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAG TAAAAATAAAAGTTGGCCGGGCATGGTGGCTCGTGCCTGTAATCCCAGCACTTTGGGAGGCCGAG A G lnc-POLR2F-2 RNACentral:URS0000D57E4D lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965200509 Functional Loss SNV dbSNP153 33..33 33 - - - 33463 RMVar_ID_33463 Human_SNP_ID_703607523 A-to-I Human chr22 + 37947891 37947891 37947891 CACTTTGGGAGGCCGAGATGGGTAATCACTTGAGGTCAGGAATTCGAGACCACCCTGGCTAACAC CACTTTGGGAGGCCGAGATGGGTAATCACTTGGGGTCAGGAATTCGAGACCACCCTGGCTAACAC A G lnc-POLR2F-2 RNACentral:URS0000D57E4D lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560990981 Functional Loss SNV dbSNP153 33..33 33 - - - 33464 RMVar_ID_33464 Human_SNP_ID_703609378 A-to-I Human chr22 + 37954484 37954484 37954484 ACCACCACGCCTTGCTAATTGCTTGTAGTTTTAGTAGAGACGGGTTTCACCATGTTGGCCAGACT ACCACCACGCCTTGCTAATTGCTTGTAGTTTTGGTAGAGACGGGTTTCACCATGTTGGCCAGACT A G POLR2F Ensembl:ENSG00000100142 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1337887193 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14480922 33465 RMVar_ID_33465 Human_SNP_ID_703609385 A-to-I Human chr22 + 37954500 37954500 37954500 AATTGCTTGTAGTTTTAGTAGAGACGGGTTTCACCATGTTGGCCAGACTGGCCTCGAACTCCTGA AATTGCTTGTAGTTTTAGTAGAGACGGGTTTCGCCATGTTGGCCAGACTGGCCTCGAACTCCTGA A G POLR2F Ensembl:ENSG00000100142 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971997157 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14480922 33466 RMVar_ID_33466 Human_SNP_ID_703611828 A-to-I Human chr22 + 37963915 37963915 37963915 CCTGAGGTCAGGAGTTCGAGAGCAGCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATAC CCTGAGGTCAGGAGTTCGAGAGCAGCCTGGCCGACATGGTGAAACCCCGTCTCTACTAAAAATAC A G POLR2F Ensembl:ENSG00000100142 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1004796287 Functional Loss SNV dbSNP153 33..33 33 - - - 33467 RMVar_ID_33467 Human_SNP_ID_703611838 A-to-I Human chr22 + 37963940 37963940 37963940 CCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCCGGGTGTGGTGGCGC CCTGGCCAACATGGTGAAACCCCGTCTCTACTGAAAATACAAAAATTAGCCGGGTGTGGTGGCGC A G POLR2F Ensembl:ENSG00000100142 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1198147544 Functional Loss SNV dbSNP153 33..33 33 - - - 33468 RMVar_ID_33468 Human_SNP_ID_703611855 A-to-I Human chr22 + 37963979 37963979 37963979 CAAAAATTAGCCGGGTGTGGTGGCGCGCGCCTATAATCCCAGCTACTCGGGAGGCTGAGGCAAGA CAAAAATTAGCCGGGTGTGGTGGCGCGCGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAAGA A G POLR2F Ensembl:ENSG00000100142 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1425736398 Functional Loss SNV dbSNP153 33..33 33 - - - 33469 RMVar_ID_33469 Human_SNP_ID_703619868 A-to-I Human chr22 + 37995731 37995731 37995731 ACAGTGGCTCACACCTGTAGTCCCAGCACTTTATGAGGCTAAGGCTGGTGGATCGCTTGAGCCCA ACAGTGGCTCACACCTGTAGTCCCAGCACTTTCTGAGGCTAAGGCTGGTGGATCGCTTGAGCCCA A C POLR2F Ensembl:ENSG00000100142 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1249987102 Functional Loss SNV dbSNP153 33..33 33 - - - 33470 RMVar_ID_33470 Human_SNP_ID_703621580 A-to-I Human chr22 + 38002993 38002993 38002993 GTGATCTGCTTGCCTCGGCCTCTCAAAGTGCTAGGATTACAGGCGTGACCCACCGCGCCCGGCCA GTGATCTGCTTGCCTCGGCCTCTCAAAGTGCTGGGATTACAGGCGTGACCCACCGCGCCCGGCCA A G POLR2F Ensembl:ENSG00000100142 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1233960380 Functional Loss SNV dbSNP153 33..33 33 - - - 33471 RMVar_ID_33471 Human_SNP_ID_703621986 A-to-I Human chr22 + 38004474 38004474 38004474 CGCTCACTGTGGGCCAGGTGCTTTCTACCTATAAGACATGCATATCTACTCGCTGAGTTCTCATG CGCTCACTGTGGGCCAGGTGCTTTCTACCTATGAGACATGCATATCTACTCGCTGAGTTCTCATG A G POLR2F Ensembl:ENSG00000100142 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,frontal_cortex - 29129909,30559470 RNA-Seq:(High) rs1023607213 Functional Loss SNV dbSNP153 33..33 33 - - - 33472 RMVar_ID_33472 Human_SNP_ID_703621990 A-to-I Human chr22 + 38004489 38004489 38004489 AGGTGCTTTCTACCTATAAGACATGCATATCTACTCGCTGAGTTCTCATGACTGCCAGAATGGAG AGGTGCTTTCTACCTATAAGACATGCATATCTCCTCGCTGAGTTCTCATGACTGCCAGAATGGAG A C POLR2F Ensembl:ENSG00000100142 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1177234635 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26675745 33473 RMVar_ID_33473 Human_SNP_ID_703621991 A-to-I Human chr22 + 38004489 38004489 38004489 AGGTGCTTTCTACCTATAAGACATGCATATCTACTCGCTGAGTTCTCATGACTGCCAGAATGGAG AGGTGCTTTCTACCTATAAGACATGCATATCTGCTCGCTGAGTTCTCATGACTGCCAGAATGGAG A G POLR2F Ensembl:ENSG00000100142 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1177234635 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26675745 33474 RMVar_ID_33474 Human_SNP_ID_703622134 A-to-I Human chr22 + 38005161 38005161 38005161 ACTCAGCGAGTAGATATGCATGTCTTTTAGGTAGAAAGCACCTGGCCCACAGTGAGCACTCAGGA ACTCAGCGAGTAGATATGCATGTCTTTTAGGTGGAAAGCACCTGGCCCACAGTGAGCACTCAGGA A G POLR2F Ensembl:ENSG00000100142 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1388614366 Functional Loss SNV dbSNP153 33..33 33 - - - 33475 RMVar_ID_33475 Human_SNP_ID_703625642 A-to-I Human chr22 + 38020091 38020091 38020091 TCCAGGTGGGCCGGCCGTGGTGGCTCATACCTATAATCCCGGCACTTTGGAAGGCTGAGGTGGGA TCCAGGTGGGCCGGCCGTGGTGGCTCATACCTGTAATCCCGGCACTTTGGAAGGCTGAGGTGGGA A G POLR2F Ensembl:ENSG00000100142 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1196237289 Functional Loss SNV dbSNP153 33..33 33 - - - 33476 RMVar_ID_33476 Human_SNP_ID_703646197 A-to-I Human chr22 + 38093121 38093121 38093121 CCAGGAGGTGGAGGTTGCAGTGAGCTGAGATCATGCCACTGCACTCCAGCCTGAGCAACAAGAGC CCAGGAGGTGGAGGTTGCAGTGAGCTGAGATCGTGCCACTGCACTCCAGCCTGAGCAACAAGAGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1259312482 Functional Loss SNV dbSNP153 33..33 33 - - - 33477 RMVar_ID_33477 Human_SNP_ID_703658754 A-to-I Human chr22 - 38135756 38135756 38135756 CGTGAGACACCGCGCCCAGCCAGAAAAATTTTAAAGTCTTCTCCTTGCACAGCTGAACTTGTGAA CGTGAGACACCGCGCCCAGCCAGAAAAATTTTGAAGTCTTCTCCTTGCACAGCTGAACTTGTGAA T C PLA2G6 Ensembl:ENSG00000184381 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs979484891 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113167,RMVar_hsa_circ_214266,RMVar_hsa_circ_16138 33478 RMVar_ID_33478 Human_SNP_ID_703677600 A-to-I Human chr22 + 38209140 38209140 38209140 CAGGCTGGAGTGCAGTGTCGCGATCTCGGCTCACTGCATGCTTCACCTCCCGGGTTCACGCCATT CAGGCTGGAGTGCAGTGTCGCGATCTCGGCTCCCTGCATGCTTCACCTCCCGGGTTCACGCCATT A C MAFF Ensembl:ENSG00000185022 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs776301380 Functional Loss SNV dbSNP153 33..33 33 - - - 33479 RMVar_ID_33479 Human_SNP_ID_703677601 A-to-I Human chr22 + 38209140 38209140 38209140 CAGGCTGGAGTGCAGTGTCGCGATCTCGGCTCACTGCATGCTTCACCTCCCGGGTTCACGCCATT CAGGCTGGAGTGCAGTGTCGCGATCTCGGCTCGCTGCATGCTTCACCTCCCGGGTTCACGCCATT A G MAFF Ensembl:ENSG00000185022 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs776301380 Functional Loss SNV dbSNP153 33..33 33 - - - 33480 RMVar_ID_33480 Human_SNP_ID_703686417 A-to-I Human chr22 - 38241431 38241431 38241431 CTTGCGCCTCGACCTCCCAAAGTGCCGGGATTATAGGCATGAGCCACTGCATCCAATGCATTTCC CTTGCGCCTCGACCTCCCAAAGTGCCGGGATTGTAGGCATGAGCCACTGCATCCAATGCATTTCC T C TMEM184B Ensembl:ENSG00000198792 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs531556738 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14482679 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 33481 RMVar_ID_33481 Human_SNP_ID_703704607 A-to-I Human chr22 - 38306999 38306999 38306999 GCCTGGCTAATATTTGTATTTTTTGTAGAGATAGGGTCTCACTATGTTGCTTAGGCTGGTCTCGA GCCTGGCTAATATTTGTATTTTTTGTAGAGATGGGGTCTCACTATGTTGCTTAGGCTGGTCTCGA T C TPTEP2-CSNK1E,CSNK1E Ensembl:ENSG00000283900,Ensembl:ENSG00000213923 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1252332667 Functional Loss SNV dbSNP153 33..33 33 - - - 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 33482 RMVar_ID_33482 Human_SNP_ID_703708756 A-to-I Human chr22 - 38322166 38322166 38322166 AGCTGGGATTACGGGCGCACATCTCCACTCCTAGCTAATGTTTGTATTTTAGTAGAGATGGGGTT AGCTGGGATTACGGGCGCACATCTCCACTCCTTGCTAATGTTTGTATTTTAGTAGAGATGGGGTT T A TPTEP2-CSNK1E Ensembl:ENSG00000283900 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs888289082 Functional Loss SNV dbSNP153 33..33 33 - - - 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 33483 RMVar_ID_33483 Human_SNP_ID_703708757 A-to-I Human chr22 - 38322166 38322166 38322166 AGCTGGGATTACGGGCGCACATCTCCACTCCTAGCTAATGTTTGTATTTTAGTAGAGATGGGGTT AGCTGGGATTACGGGCGCACATCTCCACTCCTCGCTAATGTTTGTATTTTAGTAGAGATGGGGTT T G TPTEP2-CSNK1E Ensembl:ENSG00000283900 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs888289082 Functional Loss SNV dbSNP153 33..33 33 - - - 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 33484 RMVar_ID_33484 Human_SNP_ID_703714437 A-to-I Human chr22 - 38343207 38343207 38343207 CAATGCCCGGCTAATTTTTGTATCTTTTAGTAAGTATGGGGTTTCACCATGTTGGTCGGGCTGGT CAATGCCCGGCTAATTTTTGTATCTTTTAGTATGTATGGGGTTTCACCATGTTGGTCGGGCTGGT T A TPTEP2,TPTEP2-CSNK1E Ensembl:ENSG00000244627,Ensembl:ENSG00000283900 Pseudogene,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973695344 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_214278,RMVar_hsa_circ_77501,RMVar_hsa_circ_125726,RMVar_hsa_circ_214287 33485 RMVar_ID_33485 Human_SNP_ID_703714639 A-to-I Human chr22 - 38343890 38343889 38343890 ACCTCGGCCGGGCACGGTGGCTCACGCCTGTAATCTCAGCACTTTGGGAGGCCGAGGTGGGCAGA ACCTCGGCCGGGCACGGTGGCTCACGCCTGTA_TCTCAGCACTTTGGGAGGCCGAGGTGGGCAGA AT A TPTEP2,TPTEP2-CSNK1E Ensembl:ENSG00000244627,Ensembl:ENSG00000283900 Pseudogene,Protein coding intron,intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs777970445 Functional Loss DEL dbSNP153 33..33 33 - - - Human_Splice_Rec_2166764,Human_Splice_Rec_2166765 RMVar_hsa_circ_214278,RMVar_hsa_circ_77501,RMVar_hsa_circ_125726,RMVar_hsa_circ_214287 33486 RMVar_ID_33486 Human_SNP_ID_703716507 A-to-I Human chr22 - 38350413 38350413 38350413 CCAGGAAGCAGAGGTTGCAGTGAGCCAAGATCACGACATTGCACTCCAGCCCTCCAGCCCAGGCA CCAGGAAGCAGAGGTTGCAGTGAGCCAAGATCGCGACATTGCACTCCAGCCCTCCAGCCCAGGCA T C TPTEP2,TPTEP2-CSNK1E Ensembl:ENSG00000244627,Ensembl:ENSG00000283900 Pseudogene,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1157870175 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5249830 RMVar_hsa_circ_214278,RMVar_hsa_circ_77501,RMVar_hsa_circ_125726,RMVar_hsa_circ_214287 33487 RMVar_ID_33487 Human_SNP_ID_703717321 A-to-I Human chr22 - 38352910 38352910 38352910 CTACTCGAGAGGCTGAGGCAGGAGAATGTTTGAACCTGGGAGATGGAGGTTGCAGTGAGCCGAGA CTACTCGAGAGGCTGAGGCAGGAGAATGTTTGGACCTGGGAGATGGAGGTTGCAGTGAGCCGAGA T C TPTEP2,TPTEP2-CSNK1E Ensembl:ENSG00000244627,Ensembl:ENSG00000283900 Pseudogene,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1430262456 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17400437 RMVar_hsa_circ_214278,RMVar_hsa_circ_77501,RMVar_hsa_circ_125726,RMVar_hsa_circ_214287 33488 RMVar_ID_33488 Human_SNP_ID_703717324 A-to-I Human chr22 - 38352923 38352923 38352923 CCTGCAATCCCAGCTACTCGAGAGGCTGAGGCAGGAGAATGTTTGAACCTGGGAGATGGAGGTTG CCTGCAATCCCAGCTACTCGAGAGGCTGAGGCTGGAGAATGTTTGAACCTGGGAGATGGAGGTTG T A TPTEP2,TPTEP2-CSNK1E Ensembl:ENSG00000244627,Ensembl:ENSG00000283900 Pseudogene,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1044053475 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17400437 RMVar_hsa_circ_214278,RMVar_hsa_circ_77501,RMVar_hsa_circ_125726,RMVar_hsa_circ_214287 33489 RMVar_ID_33489 Human_SNP_ID_703717783 A-to-I Human chr22 - 38354210 38354210 38354210 GAGCTCAAGCAGTCCTCCCAATTCAGCCTCCCAAGTAGCTGGGACCACAGGCACACACCATCATG GAGCTCAAGCAGTCCTCCCAATTCAGCCTCCCGAGTAGCTGGGACCACAGGCACACACCATCATG T C TPTEP2,TPTEP2-CSNK1E Ensembl:ENSG00000244627,Ensembl:ENSG00000283900 Pseudogene,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs530026235 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_214278,RMVar_hsa_circ_77501,RMVar_hsa_circ_125726,RMVar_hsa_circ_214287 33490 RMVar_ID_33490 Human_SNP_ID_703717800 A-to-I Human chr22 - 38354280 38354280 38354280 ACAGGGTCTCACTCTTGCCCAGGCTGGAGTGCAGTGGTGCGATCTTGGCTCACTGCAACCTCAAA ACAGGGTCTCACTCTTGCCCAGGCTGGAGTGCGGTGGTGCGATCTTGGCTCACTGCAACCTCAAA T C TPTEP2,TPTEP2-CSNK1E Ensembl:ENSG00000244627,Ensembl:ENSG00000283900 Pseudogene,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs963293814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2718399 RMVar_hsa_circ_214278,RMVar_hsa_circ_77501,RMVar_hsa_circ_125726,RMVar_hsa_circ_214287 33491 RMVar_ID_33491 Human_SNP_ID_703717809 A-to-I Human chr22 - 38354310 38354310 38354310 GTTTTGGTTTCATTTGTTTTTTTTAGGGGGACAGGGTCTCACTCTTGCCCAGGCTGGAGTGCAGT GTTTTGGTTTCATTTGTTTTTTTTAGGGGGACGGGGTCTCACTCTTGCCCAGGCTGGAGTGCAGT T C TPTEP2,TPTEP2-CSNK1E Ensembl:ENSG00000244627,Ensembl:ENSG00000283900 Pseudogene,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs906308778 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_245611,Human_RBP_ID_2718400,Human_RBP_ID_14484752,Human_RBP_ID_17573289 RMVar_hsa_circ_214278,RMVar_hsa_circ_77501,RMVar_hsa_circ_125726,RMVar_hsa_circ_214287 33492 RMVar_ID_33492 Human_SNP_ID_703718058 A-to-I Human chr22 - 38355176 38355176 38355176 GTCTCTACTAAAAATACAAAAATACAAAAATTAGCTGGGTGTGGTGACACGCGCCTGTAGTCCCA GTCTCTACTAAAAATACAAAAATACAAAAATTCGCTGGGTGTGGTGACACGCGCCTGTAGTCCCA T G TPTEP2,TPTEP2-CSNK1E Ensembl:ENSG00000244627,Ensembl:ENSG00000283900 Pseudogene,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1021058583 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_151718,Human_RBP_ID_25669772 RMVar_hsa_circ_214278,RMVar_hsa_circ_77501,RMVar_hsa_circ_125726,RMVar_hsa_circ_214287 33493 RMVar_ID_33493 Human_SNP_ID_703718074 A-to-I Human chr22 - 38355246 38355246 38355246 TCGGAGGCTGACGTGGGCAGATCACGAGATCAAGAGATCAAGACCATCCTGGCCAACATGGTGAA TCGGAGGCTGACGTGGGCAGATCACGAGATCAGGAGATCAAGACCATCCTGGCCAACATGGTGAA T C TPTEP2,TPTEP2-CSNK1E Ensembl:ENSG00000244627,Ensembl:ENSG00000283900 Pseudogene,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1329463833 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17400440 RMVar_hsa_circ_214278,RMVar_hsa_circ_77501,RMVar_hsa_circ_125726,RMVar_hsa_circ_214287 33494 RMVar_ID_33494 Human_SNP_ID_703718208 A-to-I Human chr22 - 38355747 38355747 38355747 CTCTACTAAAAATACAAAAGTCAGCTGGGCATAGTGGCAGGCGCCTGTAATCCCAGCTACTTGGG CTCTACTAAAAATACAAAAGTCAGCTGGGCATGGTGGCAGGCGCCTGTAATCCCAGCTACTTGGG T C TPTEP2,TPTEP2-CSNK1E Ensembl:ENSG00000244627,Ensembl:ENSG00000283900 Pseudogene,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs5757059 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_214278,RMVar_hsa_circ_77501,RMVar_hsa_circ_125726,RMVar_hsa_circ_214287 33495 RMVar_ID_33495 Human_SNP_ID_703718232 A-to-I Human chr22 - 38355868 38355868 38355868 GAGTCAGGAGCTAGGCACGGTGGTTCACGCCTATAATCCCAGCACTTTGGGAGGCCGAGGTGGGT GAGTCAGGAGCTAGGCACGGTGGTTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGT T C TPTEP2,TPTEP2-CSNK1E Ensembl:ENSG00000244627,Ensembl:ENSG00000283900 Pseudogene,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1183761578 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3679289,Human_RBP_ID_14484781,Human_RBP_ID_17400441 RMVar_hsa_circ_214278,RMVar_hsa_circ_77501,RMVar_hsa_circ_125726,RMVar_hsa_circ_214287 33496 RMVar_ID_33496 Human_SNP_ID_703718399 A-to-I Human chr22 - 38356485 38356485 38356485 TCGCCCAGGCTGGAGTGCAGTGGTATGATCTCAGCTCACTGCAACCTCTGAGTCCCAGGTTCAAG TCGCCCAGGCTGGAGTGCAGTGGTATGATCTCGGCTCACTGCAACCTCTGAGTCCCAGGTTCAAG T C TPTEP2,TPTEP2-CSNK1E Ensembl:ENSG00000244627,Ensembl:ENSG00000283900 Pseudogene,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1295292070 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5249843,Human_RBP_ID_17400443 RMVar_hsa_circ_214278,RMVar_hsa_circ_77501,RMVar_hsa_circ_125726,RMVar_hsa_circ_214287 33497 RMVar_ID_33497 Human_SNP_ID_703751540 A-to-I Human chr22 - 38483869 38483869 38483869 AAACTATTATGGCCTGAGCACAGCTGAAATCTAGCAGAGTTTAACTCTTCTGCCTCCATGTCTGT AAACTATTATGGCCTGAGCACAGCTGAAATCTCGCAGAGTTTAACTCTTCTGCCTCCATGTCTGT T G DDX17 Ensembl:ENSG00000100201 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1455745708 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_580156,Human_RBP_ID_1611556,Human_RBP_ID_1942766,Human_RBP_ID_2718673,Human_RBP_ID_3672772,Human_RBP_ID_7081422,Human_RBP_ID_8550215,Human_RBP_ID_10051795,Human_RBP_ID_14485403,Human_RBP_ID_17193578,Human_RBP_ID_17285979,Human_RBP_ID_17399161,Human_RBP_ID_17515167,Human_RBP_ID_18329245,Human_RBP_ID_20717091,Human_RBP_ID_22820602,Human_RBP_ID_23013160,Human_RBP_ID_24425947,Human_RBP_ID_24494754,Human_RBP_ID_25669973,Human_RBP_ID_26501478,Human_RBP_ID_27037567,Human_RBP_ID_27307980 Human_miRNA_ID_2619463 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,RMVar_hsa_circ_214303 33498 RMVar_ID_33498 Human_SNP_ID_703751547 A-to-I Human chr22 + 38483894 38483891 38483894 ACTCTGCTAGATTTCAGCTGTGCTCAGGCCATAATAGTTTTTGAGGTTTGGAATTTACTGTTATT ACTCTGCTAGATTTCAGCTGTGCTCAGGCC___ATAGTTTTTGAGGTTTGGAATTTACTGTTATT CATA C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs753163894 Functional Loss DEL dbSNP153 31..33 33 - - - 33499 RMVar_ID_33499 Human_SNP_ID_703751549 A-to-I Human chr22 + 38483894 38483894 38483894 ACTCTGCTAGATTTCAGCTGTGCTCAGGCCATAATAGTTTTTGAGGTTTGGAATTTACTGTTATT ACTCTGCTAGATTTCAGCTGTGCTCAGGCCATCATAGTTTTTGAGGTTTGGAATTTACTGTTATT A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1253902586 Functional Loss SNV dbSNP153 33..33 33 - - - 33500 RMVar_ID_33500 Human_SNP_ID_703775939 A-to-I Human chr22 - 38580085 38580085 38580085 GAGACCTTGTCTCTACAAAAAAAGTAAAAATTAGCAGAGCAAGGTGGCATACGCCTGTAGTCCTA GAGACCTTGTCTCTACAAAAAAAGTAAAAATTGGCAGAGCAAGGTGGCATACGCCTGTAGTCCTA T C FAM227A Ensembl:ENSG00000184949 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223821948 Functional Loss SNV dbSNP153 33..33 33 - - - 33501 RMVar_ID_33501 Human_SNP_ID_703777036 A-to-I Human chr22 - 38584754 38584753 38584755 AACTAAATTAAATTTTTTAGAGGCAGACTCTCAGTCTGTTGTCCAGGCTGGAATGCAGTGGCGCA AACTAAATTAAATTTTTTAGAGGCAGACTCT__GTCTGTTGTCCAGGCTGGAATGCAGTGGCGCA CTG C FAM227A Ensembl:ENSG00000184949 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1300651200 Functional Loss DEL dbSNP153 32..33 33 - - - 33502 RMVar_ID_33502 Human_SNP_ID_703777090 A-to-I Human chr22 - 38584934 38584934 38584934 AAATTAGCTGGATGTTGTGGCGGGCACCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGAAGAA AAATTAGCTGGATGTTGTGGCGGGCACCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGAAGAA T C FAM227A Ensembl:ENSG00000184949 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs931745240 Functional Loss SNV dbSNP153 33..33 33 - - - 33503 RMVar_ID_33503 Human_SNP_ID_703789984 A-to-I Human chr22 - 38633565 38633565 38633565 TGCACTCCAGTCTGGGGATATAGTGAGACTCCATCTCAAACAAACAAAAAAATATTATAGTTGTT TGCACTCCAGTCTGGGGATATAGTGAGACTCCGTCTCAAACAAACAAAAAAATATTATAGTTGTT T C FAM227A Ensembl:ENSG00000184949 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1173622589 Functional Loss SNV dbSNP153 33..33 33 - - - 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 33504 RMVar_ID_33504 Human_SNP_ID_703798293 A-to-I Human chr22 + 38662560 38662560 38662560 TCACCCAAGCTGGAGTGCAGTGTCATAATCTCAGCTCACTGCAACCTCTGGCTCCTGGGCGCAAG TCACCCAAGCTGGAGTGCAGTGTCATAATCTCCGCTCACTGCAACCTCTGGCTCCTGGGCGCAAG A C CBY1 Ensembl:ENSG00000100211 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs557473952 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17572823 33505 RMVar_ID_33505 Human_SNP_ID_703798300 A-to-I Human chr22 + 38662594 38662594 38662594 CTCACTGCAACCTCTGGCTCCTGGGCGCAAGCAATCCTCCCACCTCTGCCTCCTGAATAGCTGGG CTCACTGCAACCTCTGGCTCCTGGGCGCAAGCTATCCTCCCACCTCTGCCTCCTGAATAGCTGGG A T CBY1 Ensembl:ENSG00000100211 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1448834711 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17572823 33506 RMVar_ID_33506 Human_SNP_ID_703798469 A-to-I Human chr22 + 38663440 38663440 38663440 AAAAGAGGCCGGACGCGGTGGCCCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGTGG AAAAGAGGCCGGACGCGGTGGCCCACACCTGTGATCCCAGCACTTTGGGAGGCTGAGGTGGGTGG A G CBY1 Ensembl:ENSG00000100211 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1284048145 Functional Loss SNV dbSNP153 33..33 33 - - - 33507 RMVar_ID_33507 Human_SNP_ID_703798914 A-to-I Human chr22 + 38665201 38665201 38665201 AAACTGGAAACAGGCCGGGTGTGGTGGTTCATACCTGTAATTCCAGCATTTTGGGAGGCTGAGGC AAACTGGAAACAGGCCGGGTGTGGTGGTTCATGCCTGTAATTCCAGCATTTTGGGAGGCTGAGGC A G CBY1 Ensembl:ENSG00000100211 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1201743121 Functional Loss SNV dbSNP153 33..33 33 - - - 33508 RMVar_ID_33508 Human_SNP_ID_703798915 A-to-I Human chr22 + 38665207 38665207 38665207 GAAACAGGCCGGGTGTGGTGGTTCATACCTGTAATTCCAGCATTTTGGGAGGCTGAGGCAGGCAG GAAACAGGCCGGGTGTGGTGGTTCATACCTGTCATTCCAGCATTTTGGGAGGCTGAGGCAGGCAG A C CBY1 Ensembl:ENSG00000100211 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1247330039 Functional Loss SNV dbSNP153 33..33 33 - - - 33509 RMVar_ID_33509 Human_SNP_ID_703799199 A-to-I Human chr22 + 38666348 38666348 38666348 GTAATCCTCCCTCCCTGGCCTCCCAAAGTGCTAGGATTACAGGTGTGAGCCACTGCTCCCAGCCT GTAATCCTCCCTCCCTGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACTGCTCCCAGCCT A G CBY1 Ensembl:ENSG00000100211 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1195141983 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_351463 33510 RMVar_ID_33510 Human_SNP_ID_703800766 A-to-I Human chr22 + 38672499 38672499 38672499 CACCACGCTTGGCTAATTTTTGCATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGG CACCACGCTTGGCTAATTTTTGCATTTTTAGTGGAGATGGGGTTTCACCATGTTGGCCAGGCTGG A G CBY1 Ensembl:ENSG00000100211 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs189384904 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80722,RMVar_hsa_circ_78598,RMVar_hsa_circ_214350,RMVar_hsa_circ_214351 33511 RMVar_ID_33511 Human_SNP_ID_703802221 A-to-I Human chr22 + 38677988 38677988 38677988 CACCACATCTGGCTAATTTTTGTGTTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGATGG CACCACATCTGGCTAATTTTTGTGTTTTTAGTGGAGATGGGGTTTCACCATGTTGGCCAGGATGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1193069694 Functional Loss SNV dbSNP153 33..33 33 - - - 33512 RMVar_ID_33512 Human_SNP_ID_703807069 A-to-I Human chr22 - 38695524 38695524 38695524 AGGATGGCTTGAGTCCAGGAGGTCGAGGCTGCAGTGAGCCATGTTCGTGCCACTGCATTCCAGCC AGGATGGCTTGAGTCCAGGAGGTCGAGGCTGCGGTGAGCCATGTTCGTGCCACTGCATTCCAGCC T C JOSD1 Ensembl:ENSG00000100221 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1374514607 Functional Loss SNV dbSNP153 33..33 33 - - - 33513 RMVar_ID_33513 Human_SNP_ID_703807101 A-to-I Human chr22 - 38695646 38695646 38695646 GTCCAGCAGTTTGAGACCAGCCCGTGCAACATAGTGAGACCCTATCTCTACAAAAAATTTAAAAA GTCCAGCAGTTTGAGACCAGCCCGTGCAACATGGTGAGACCCTATCTCTACAAAAAATTTAAAAA T C JOSD1 Ensembl:ENSG00000100221 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs59244506 Functional Loss SNV dbSNP153 33..33 33 - - - 33514 RMVar_ID_33514 Human_SNP_ID_703809980 A-to-I Human chr22 + 38704572 38704572 38704572 TACCCGTCTCAGCCTCCCAAAGTGCTGGGATTACAAGTGTGAGCCATTGCTCCCGGCCCATATAG TACCCGTCTCAGCCTCCCAAAGTGCTGGGATTTCAAGTGTGAGCCATTGCTCCCGGCCCATATAG A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1317187153 Functional Loss SNV dbSNP153 33..33 33 - - - 33515 RMVar_ID_33515 Human_SNP_ID_703809981 A-to-I Human chr22 + 38704574 38704574 38704574 CCCGTCTCAGCCTCCCAAAGTGCTGGGATTACAAGTGTGAGCCATTGCTCCCGGCCCATATAGGA CCCGTCTCAGCCTCCCAAAGTGCTGGGATTACTAGTGTGAGCCATTGCTCCCGGCCCATATAGGA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1214411992 Functional Loss SNV dbSNP153 33..33 33 - - - 33516 RMVar_ID_33516 Human_SNP_ID_703811745 A-to-I Human chr22 + 38711584 38711584 38711584 TGAGATTTCTTTGAAAAAGAAGACTCATGCCTATAATCCCAGCACTTTGGGAGGCCAAGGTGGGC TGAGATTTCTTTGAAAAAGAAGACTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGC A G GTPBP1 Ensembl:ENSG00000100226 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1047639538 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93252,RMVar_hsa_circ_375639,RMVar_hsa_circ_214356,RMVar_hsa_circ_214357 33517 RMVar_ID_33517 Human_SNP_ID_703814415 A-to-I Human chr22 - 38722784 38722784 38722784 CTGGACACTGGATTCTCCTACAATCAAGCCAAATCCAGCTGCTTCCAAAGAGTACTTTCAGAAGG CTGGACACTGGATTCTCCTACAATCAAGCCAAGTCCAGCTGCTTCCAAAGAGTACTTTCAGAAGG T C PRDX3P1 Ensembl:ENSG00000229598 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879228285 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18535384 Human_miRNA_ID_1822490 33518 RMVar_ID_33518 Human_SNP_ID_703814417 A-to-I Human chr22 - 38722795 38722795 38722795 TGCCCAGCAAACTGGACACTGGATTCTCCTACAATCAAGCCAAATCCAGCTGCTTCCAAAGAGTA TGCCCAGCAAACTGGACACTGGATTCTCCTACGATCAAGCCAAATCCAGCTGCTTCCAAAGAGTA T C PRDX3P1 Ensembl:ENSG00000229598 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879110107 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18535384 Human_miRNA_ID_1822490,Human_miRNA_ID_1885342 33519 RMVar_ID_33519 Human_SNP_ID_703814428 A-to-I Human chr22 - 38722819 38722819 38722819 TATGTAGAAACCCATGGAGAAGTCTGCCCAGCAAACTGGACACTGGATTCTCCTACAATCAAGCC TATGTAGAAACCCATGGAGAAGTCTGCCCAGCGAACTGGACACTGGATTCTCCTACAATCAAGCC T C PRDX3P1 Ensembl:ENSG00000229598 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879036445 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1828728,Human_miRNA_ID_1837612,Human_miRNA_ID_1838040,Human_miRNA_ID_1888590 33520 RMVar_ID_33520 Human_SNP_ID_703840994 A-to-I Human chr22 - 38821023 38821023 38821023 TGGTTAGGTGGTGCATGCCTGTAGTCCCAGCTACTCGGGAGGCCGAGGCAGAAGAATCTCTTGAA TGGTTAGGTGGTGCATGCCTGTAGTCCCAGCTGCTCGGGAGGCCGAGGCAGAAGAATCTCTTGAA T C NPTXR Ensembl:ENSG00000221890 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946574467 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92374,RMVar_hsa_circ_214375 33521 RMVar_ID_33521 Human_SNP_ID_703893307 A-to-I Human chr22 + 39018817 39018814 39018817 CAGGCTGGGTCACATGACAAAGCCCCATCTCTACAAAAAAAAAAAAAAAAAAAAAAAAAAAGCCA CAGGCTGGGTCACATGACAAAGCCCCATCT___CAAAAAAAAAAAAAAAAAAAAAAAAAAAGCCA TCTA T APOBEC3C,AL022318.4 Ensembl:ENSG00000244509,Ensembl:ENSG00000284554 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1212666428 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_5324784 RMVar_hsa_circ_214381,RMVar_hsa_circ_113483 33522 RMVar_ID_33522 Human_SNP_ID_703893309 A-to-I Human chr22 + 39018817 39018817 39018817 CAGGCTGGGTCACATGACAAAGCCCCATCTCTACAAAAAAAAAAAAAAAAAAAAAAAAAAAGCCA CAGGCTGGGTCACATGACAAAGCCCCATCTCTCCAAAAAAAAAAAAAAAAAAAAAAAAAAAGCCA A C APOBEC3C,AL022318.4 Ensembl:ENSG00000244509,Ensembl:ENSG00000284554 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1311022954 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5324784 RMVar_hsa_circ_214381,RMVar_hsa_circ_113483 33523 RMVar_ID_33523 Human_SNP_ID_703893610 A-to-I Human chr22 + 39019867 39019867 39019867 TGCTCCTCTTGTCCAGGCTGGAATGCAATGGCACAATCTGGACTCACTGCAACCTCCGCCTCCCG TGCTCCTCTTGTCCAGGCTGGAATGCAATGGCGCAATCTGGACTCACTGCAACCTCCGCCTCCCG A G APOBEC3C,AL022318.4 Ensembl:ENSG00000244509,Ensembl:ENSG00000284554 Protein coding,Protein coding 3'UTR,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1139727 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17986471,Human_RBP_ID_26498602 RMVar_hsa_circ_214381,RMVar_hsa_circ_113483 33524 RMVar_ID_33524 Human_SNP_ID_703893617 A-to-I Human chr22 + 39019900 39019900 39019900 CAATCTGGACTCACTGCAACCTCCGCCTCCCGAGTTTAAGCGATTCTTCTGCTTCAGCCTCCCGA CAATCTGGACTCACTGCAACCTCCGCCTCCCGGGTTTAAGCGATTCTTCTGCTTCAGCCTCCCGA A G APOBEC3C,AL022318.4 Ensembl:ENSG00000244509,Ensembl:ENSG00000284554 Protein coding,Protein coding 3'UTR,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1139728 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_214381,RMVar_hsa_circ_113483 33525 RMVar_ID_33525 Human_SNP_ID_703893620 A-to-I Human chr22 + 39019905 39019905 39019905 TGGACTCACTGCAACCTCCGCCTCCCGAGTTTAAGCGATTCTTCTGCTTCAGCCTCCCGAGTAAA TGGACTCACTGCAACCTCCGCCTCCCGAGTTTGAGCGATTCTTCTGCTTCAGCCTCCCGAGTAAA A G APOBEC3C,AL022318.4 Ensembl:ENSG00000244509,Ensembl:ENSG00000284554 Protein coding,Protein coding 3'UTR,intron GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-Seq:(High) rs1139729 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26498603 RMVar_hsa_circ_214381,RMVar_hsa_circ_113483 33526 RMVar_ID_33526 Human_SNP_ID_703893644 A-to-I Human chr22 + 39019979 39019979 39019979 TCACCACACCTGGTTAATTTTGTAGTTTTAGTAGAGATGGGGTCTCACCATGTTGGCCAGACTGG TCACCACACCTGGTTAATTTTGTAGTTTTAGTGGAGATGGGGTCTCACCATGTTGGCCAGACTGG A G APOBEC3C,AL022318.4 Ensembl:ENSG00000244509,Ensembl:ENSG00000284554 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1208757421 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_214381,RMVar_hsa_circ_113483 33527 RMVar_ID_33527 Human_SNP_ID_703893658 A-to-I Human chr22 + 39020030 39020030 39020030 GTTGGCCAGACTGGTCTCGAACTCCTGACCTCAGGTGATCCGCCTGTCTCAGCCTCTCCAAGTGC GTTGGCCAGACTGGTCTCGAACTCCTGACCTCGGGTGATCCGCCTGTCTCAGCCTCTCCAAGTGC A G APOBEC3C,AL022318.4 Ensembl:ENSG00000244509,Ensembl:ENSG00000284554 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-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 33528 RMVar_ID_33528 Human_SNP_ID_703893666 A-to-I Human chr22 + 39020076 39020076 39020076 TCTCAGCCTCTCCAAGTGCTGGGATTACAGGCATCAGCCACTATGCCCGGCTGGGATCATATGTT TCTCAGCCTCTCCAAGTGCTGGGATTACAGGCGTCAGCCACTATGCCCGGCTGGGATCATATGTT A G APOBEC3C,AL022318.4 Ensembl:ENSG00000244509,Ensembl:ENSG00000284554 Protein coding,Protein coding 3'UTR,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-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 33529 RMVar_ID_33529 Human_SNP_ID_703893667 A-to-I Human chr22 + 39020076 39020076 39020076 TCTCAGCCTCTCCAAGTGCTGGGATTACAGGCATCAGCCACTATGCCCGGCTGGGATCATATGTT TCTCAGCCTCTCCAAGTGCTGGGATTACAGGCTTCAGCCACTATGCCCGGCTGGGATCATATGTT A T APOBEC3C,AL022318.4 Ensembl:ENSG00000244509,Ensembl:ENSG00000284554 Protein coding,Protein coding 3'UTR,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-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 33530 RMVar_ID_33530 Human_SNP_ID_703895875 A-to-I Human chr22 + 39026869 39026869 39026869 CTGCCTCCCGGTTCTAGCAATTCCCTTGTCTCAGCCTCCCAAGTACCTGGGATTACAGGCTCATG CTGCCTCCCGGTTCTAGCAATTCCCTTGTCTCGGCCTCCCAAGTACCTGGGATTACAGGCTCATG A G APOBEC3D,AL022318.4 Ensembl:ENSG00000243811,Ensembl:ENSG00000284554 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1300920108 Functional Loss SNV dbSNP153 33..33 33 - - - 33531 RMVar_ID_33531 Human_SNP_ID_703895876 A-to-I Human chr22 + 39026869 39026869 39026869 CTGCCTCCCGGTTCTAGCAATTCCCTTGTCTCAGCCTCCCAAGTACCTGGGATTACAGGCTCATG CTGCCTCCCGGTTCTAGCAATTCCCTTGTCTCTGCCTCCCAAGTACCTGGGATTACAGGCTCATG A T APOBEC3D,AL022318.4 Ensembl:ENSG00000243811,Ensembl:ENSG00000284554 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1300920108 Functional Loss SNV dbSNP153 33..33 33 - - - 33532 RMVar_ID_33532 Human_SNP_ID_703896491 A-to-I Human chr22 + 39028874 39028874 39028874 GGAGATTTGCTTGAAACCAGGAGGCGGAAGTTATAGTGAGCCGAGATTGCACCACTGCACTCCAG GGAGATTTGCTTGAAACCAGGAGGCGGAAGTTGTAGTGAGCCGAGATTGCACCACTGCACTCCAG A G APOBEC3D,AL022318.4 Ensembl:ENSG00000243811,Ensembl:ENSG00000284554 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs558698533 Functional Loss SNV dbSNP153 33..33 33 - - - 33533 RMVar_ID_33533 Human_SNP_ID_703897154 A-to-I Human chr22 + 39031029 39031029 39031029 CTCTACTAAAACTACAAAAATTAGCCAGGCGTAGGAGTGCGCGACTGTAATCCTAGCTACTCCGG CTCTACTAAAACTACAAAAATTAGCCAGGCGTGGGAGTGCGCGACTGTAATCCTAGCTACTCCGG A G APOBEC3D,AL022318.4 Ensembl:ENSG00000243811,Ensembl:ENSG00000284554 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1300505176 Functional Loss SNV dbSNP153 33..33 33 - - - 33534 RMVar_ID_33534 Human_SNP_ID_703897155 A-to-I Human chr22 + 39031029 39031029 39031029 CTCTACTAAAACTACAAAAATTAGCCAGGCGTAGGAGTGCGCGACTGTAATCCTAGCTACTCCGG CTCTACTAAAACTACAAAAATTAGCCAGGCGTTGGAGTGCGCGACTGTAATCCTAGCTACTCCGG A T APOBEC3D,AL022318.4 Ensembl:ENSG00000243811,Ensembl:ENSG00000284554 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1300505176 Functional Loss SNV dbSNP153 33..33 33 - - - 33535 RMVar_ID_33535 Human_SNP_ID_703897853 A-to-I Human chr22 + 39032798 39032798 39032798 TTTTTTTTTTTTTTTTTTTTTGTATTTTTAGTAGTGACTGGGTTTCACCATGTTGGCCAGGCTGG TTTTTTTTTTTTTTTTTTTTTGTATTTTTAGTTGTGACTGGGTTTCACCATGTTGGCCAGGCTGG A T APOBEC3D,AL022318.4 Ensembl:ENSG00000243811,Ensembl:ENSG00000284554 Protein coding,Protein coding 3'UTR,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1354811257 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26500298 33536 RMVar_ID_33536 Human_SNP_ID_703897944 A-to-I Human chr22 + 39033060 39033060 39033060 CACGACAAAGCCCCATTTCTACAAAAAAAAATACCAAAAAAAAGCCAGATGTGGTGGCATGCACC CACGACAAAGCCCCATTTCTACAAAAAAAAATTCCAAAAAAAAGCCAGATGTGGTGGCATGCACC A T APOBEC3D,AL022318.4 Ensembl:ENSG00000243811,Ensembl:ENSG00000284554 Protein coding,Protein coding 3'UTR,3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1031010211 Functional Loss SNV dbSNP153 33..33 33 - - - 33537 RMVar_ID_33537 Human_SNP_ID_703897956 A-to-I Human chr22 + 39033096 39033093 39033096 AAAAAAAGCCAGATGTGGTGGCATGCACCTGTAGTTTAAGCTACTTGGGAGGATGAAGTGGGAGG AAAAAAAGCCAGATGTGGTGGCATGCACCT___GTTTAAGCTACTTGGGAGGATGAAGTGGGAGG TGTA T APOBEC3D,AL022318.4 Ensembl:ENSG00000243811,Ensembl:ENSG00000284554 Protein coding,Protein coding 3'UTR,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1483755573 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_26500301 33538 RMVar_ID_33538 Human_SNP_ID_703898176 A-to-I Human chr22 + 39033829 39033829 39033829 TTGCCCATGCCAGGCTTATTTTTATTTTTTTCAGATGAAGTCTTGCTCTGTCACCCAGGCTGGAG TTGCCCATGCCAGGCTTATTTTTATTTTTTTCTGATGAAGTCTTGCTCTGTCACCCAGGCTGGAG A T - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1435403281 Functional Loss SNV dbSNP153 33..33 33 - - - 33539 RMVar_ID_33539 Human_SNP_ID_703898733 A-to-I Human chr22 + 39035776 39035776 39035776 TACTGAAAGTGCAAAAAGTAGCTGGGCATGGTAGTGGGCACCTGTAATCCCAGCTACTCGGGAGG TACTGAAAGTGCAAAAAGTAGCTGGGCATGGTCGTGGGCACCTGTAATCCCAGCTACTCGGGAGG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1276932318 Functional Loss SNV dbSNP153 33..33 33 - - - 33540 RMVar_ID_33540 Human_SNP_ID_703901198 A-to-I Human chr22 + 39043904 39043902 39043904 AAAATTAGCCCGGTGTGGTGGCAGTCGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGA AAAATTAGCCCGGTGTGGTGGCAGTCGCCTG__ATCCCAGCTACTTGGGAGGCTGAGGCAGGAGA GTA G APOBEC3F Ensembl:ENSG00000128394 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1429046780 Functional Loss DEL dbSNP153 32..33 33 - - - 33541 RMVar_ID_33541 Human_SNP_ID_703902192 A-to-I Human chr22 + 39046742 39046742 39046742 TGGTTCTAGCAATTCTCTTGTCTCAGCCTCCCAAGTACCTGGGATTACAGGCTCATGCCACCACA TGGTTCTAGCAATTCTCTTGTCTCAGCCTCCCGAGTACCTGGGATTACAGGCTCATGCCACCACA A G APOBEC3F Ensembl:ENSG00000128394 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1197766959 Functional Loss SNV dbSNP153 33..33 33 - - - 33542 RMVar_ID_33542 Human_SNP_ID_703902197 A-to-I Human chr22 + 39046781 39046781 39046781 TGGGATTACAGGCTCATGCCACCACACTGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTTG TGGGATTACAGGCTCATGCCACCACACTGGCTGATTTTTGTATTTTTAGTAGAGACGGGGTTTTG A G APOBEC3F Ensembl:ENSG00000128394 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs548116226 Functional Loss SNV dbSNP153 33..33 33 - - - 33543 RMVar_ID_33543 Human_SNP_ID_703903153 A-to-I Human chr22 + 39049841 39049841 39049841 TCTGTCTCAGCCTCCTGAGTAGCTGGGATTACAGGTGCCCACCACCACACCCAGCTAATTTTTAT TCTGTCTCAGCCTCCTGAGTAGCTGGGATTACGGGTGCCCACCACCACACCCAGCTAATTTTTAT A G APOBEC3F Ensembl:ENSG00000128394 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1249682122 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102365,RMVar_hsa_circ_214382 33544 RMVar_ID_33544 Human_SNP_ID_703903158 A-to-I Human chr22 + 39049865 39049865 39049865 GGGATTACAGGTGCCCACCACCACACCCAGCTAATTTTTATTCCATTTTTAGTAGAGACGGGGTT GGGATTACAGGTGCCCACCACCACACCCAGCTGATTTTTATTCCATTTTTAGTAGAGACGGGGTT A G APOBEC3F Ensembl:ENSG00000128394 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs532897377 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102365,RMVar_hsa_circ_214382 33545 RMVar_ID_33545 Human_SNP_ID_703903200 A-to-I Human chr22 + 39049971 39049971 39049971 GTGATCCGCCCCCCTCGGCCTCCCAAAGTGCTAGGATTACAGGCATGAGCCACCACGCCCAACTT GTGATCCGCCCCCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCACGCCCAACTT A G APOBEC3F Ensembl:ENSG00000128394 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1273233286 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102365,RMVar_hsa_circ_214382 33546 RMVar_ID_33546 Human_SNP_ID_703903527 A-to-I Human chr22 + 39051147 39051147 39051147 TAGTCCCAGCTACTTGGGTGGCTTAGGCAGGAAAATCGCCTGAACCCAGGAGGCAGAGGTTGCAG TAGTCCCAGCTACTTGGGTGGCTTAGGCAGGAGAATCGCCTGAACCCAGGAGGCAGAGGTTGCAG A G APOBEC3F Ensembl:ENSG00000128394 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1199694691 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102365,RMVar_hsa_circ_214382 33547 RMVar_ID_33547 Human_SNP_ID_703903781 A-to-I Human chr22 + 39051833 39051833 39051833 AAAATTAGGCAGGCGTGGTGGCACGCACCTGCAGTCCCAGCTAATCAGGAGGCTGAGGTGGGAAG AAAATTAGGCAGGCGTGGTGGCACGCACCTGCGGTCCCAGCTAATCAGGAGGCTGAGGTGGGAAG A G APOBEC3F Ensembl:ENSG00000128394 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs35281599 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102365,RMVar_hsa_circ_214382 33548 RMVar_ID_33548 Human_SNP_ID_703903782 A-to-I Human chr22 + 39051833 39051833 39051833 AAAATTAGGCAGGCGTGGTGGCACGCACCTGCAGTCCCAGCTAATCAGGAGGCTGAGGTGGGAAG AAAATTAGGCAGGCGTGGTGGCACGCACCTGCTGTCCCAGCTAATCAGGAGGCTGAGGTGGGAAG A T APOBEC3F Ensembl:ENSG00000128394 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs35281599 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102365,RMVar_hsa_circ_214382 33549 RMVar_ID_33549 Human_SNP_ID_703904311 A-to-I Human chr22 + 39053012 39053003 39053013 AACCTAATATTTTTTTTTTTTTTTTGAGACGGAATTTCGCTCTGTCACCCAGACTGGAGTGCAAT AACCTAATATTTTTTTTTTTTTTT__________TTTCGCTCTGTCACCCAGACTGGAGTGCAAT TTGAGACGGAA T APOBEC3F Ensembl:ENSG00000128394 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1385959309 Functional Loss DEL dbSNP153 25..34 33 - - - 33550 RMVar_ID_33550 Human_SNP_ID_703904319 A-to-I Human chr22 + 39053012 39053012 39053012 AACCTAATATTTTTTTTTTTTTTTTGAGACGGAATTTCGCTCTGTCACCCAGACTGGAGTGCAAT AACCTAATATTTTTTTTTTTTTTTTGAGACGGCATTTCGCTCTGTCACCCAGACTGGAGTGCAAT A C APOBEC3F Ensembl:ENSG00000128394 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1246387983 Functional Loss SNV dbSNP153 33..33 33 - - - 33551 RMVar_ID_33551 Human_SNP_ID_703904352 A-to-I Human chr22 + 39053116 39053116 39053116 TCAAGCGATTCTCCTGCCTCCGCCTCCCGAGTAGCTGGAATTACAGACGCCTGCCACCACGCACA TCAAGCGATTCTCCTGCCTCCGCCTCCCGAGTGGCTGGAATTACAGACGCCTGCCACCACGCACA A G APOBEC3F Ensembl:ENSG00000128394 Protein coding 3'UTR GSE47997;GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,24183664,31158229,31158229,31158229 RNA-Seq:(High) rs766146094 Functional Loss SNV dbSNP153 33..33 33 - - - 33552 RMVar_ID_33552 Human_SNP_ID_703904424 A-to-I Human chr22 + 39053349 39053349 39053349 TCACCCTAGGCTGGCCGCGGTGACTCATGCCTATAATCCCCCAGCAATTTGGGAGGCAGAGGTGA TCACCCTAGGCTGGCCGCGGTGACTCATGCCTGTAATCCCCCAGCAATTTGGGAGGCAGAGGTGA A G APOBEC3F Ensembl:ENSG00000128394 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,31158229,31158229 RNA-Seq:(High) rs879430044 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26500302 33553 RMVar_ID_33553 Human_SNP_ID_703904478 A-to-I Human chr22 + 39053494 39053494 39053494 AAAAAAAAACAGGTGTGGTGGCATGCACCTGTAGTTGAAGCTACTTGGAAGGATGAAGTGGGAGG AAAAAAAAACAGGTGTGGTGGCATGCACCTGTGGTTGAAGCTACTTGGAAGGATGAAGTGGGAGG A G APOBEC3F Ensembl:ENSG00000128394 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,31158229,31158229 RNA-Seq:(High) rs752811751 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26501085 33554 RMVar_ID_33554 Human_SNP_ID_703904492 A-to-I Human chr22 + 39053570 39053570 39053570 CGGGGAGGTGGAGGCTGCAGTGAACTGAGATCACGTCACTGAACTCCAGTCTGAGCAACAGATCG CGGGGAGGTGGAGGCTGCAGTGAACTGAGATCGCGTCACTGAACTCCAGTCTGAGCAACAGATCG A G APOBEC3F Ensembl:ENSG00000128394 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1221748185 Functional Loss SNV dbSNP153 33..33 33 - - - 33555 RMVar_ID_33555 Human_SNP_ID_703904595 A-to-I Human chr22 + 39053990 39053990 39053990 CAACCCTTCCTAGTGCCCATGGGCTTTCCCATAGGACAAGAGAACATTTCTCCTTTTCTTTTTTT CAACCCTTCCTAGTGCCCATGGGCTTTCCCATGGGACAAGAGAACATTTCTCCTTTTCTTTTTTT A G APOBEC3F Ensembl:ENSG00000128394 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1448845030 Functional Loss SNV dbSNP153 33..33 33 - - - 33556 RMVar_ID_33556 Human_SNP_ID_703904679 A-to-I Human chr22 + 39054295 39054295 39054295 GCTCTGTTGCCCAGGCTGGGGTGCAGTGGTGCAATCTGGGTTCACTGCAGCCTCTGCCGCCTGAG GCTCTGTTGCCCAGGCTGGGGTGCAGTGGTGCGATCTGGGTTCACTGCAGCCTCTGCCGCCTGAG A G APOBEC3F Ensembl:ENSG00000128394 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1163402634 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26500303 33557 RMVar_ID_33557 Human_SNP_ID_703904921 A-to-I Human chr22 + 39055212 39055212 39055212 CTCGTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCGTGTGCCACCACGCCTGGCTAATTTTG CTCGTGCCTCAGCCTCCTGAGTAGCTGGGACTCCAGGCGTGTGCCACCACGCCTGGCTAATTTTG A C APOBEC3F Ensembl:ENSG00000128394 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1461093824 Functional Loss SNV dbSNP153 33..33 33 - - - 33558 RMVar_ID_33558 Human_SNP_ID_703911498 A-to-I Human chr22 + 39079394 39079394 39079394 GGCTGGAGTGCAATGACGCGATCTCGGCTCACAGCAACCTCTGCCTCCTGGGTTCAAGCGATGCT GGCTGGAGTGCAATGACGCGATCTCGGCTCACGGCAACCTCTGCCTCCTGGGTTCAAGCGATGCT A G APOBEC3G Ensembl:ENSG00000239713 Protein coding exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1442497285 Functional Loss SNV dbSNP153 33..33 33 - - - 33559 RMVar_ID_33559 Human_SNP_ID_703911556 A-to-I Human chr22 + 39079557 39079557 39079557 ATTCACCAGGCTGGTCTCGAACTTCTGACCTCAGGTGATCCACCTGCCTCGGCCTCCCAAAGTGT ATTCACCAGGCTGGTCTCGAACTTCTGACCTCGGGTGATCCACCTGCCTCGGCCTCCCAAAGTGT A G APOBEC3G Ensembl:ENSG00000239713 Protein coding exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1037032459 Functional Loss SNV dbSNP153 33..33 33 - - - 33560 RMVar_ID_33560 Human_SNP_ID_703911614 A-to-I Human chr22 + 39079801 39079801 39079801 TCGCACCTCTAATCCCAGCACTTTGGGAGGCCAAGGCGGGCAGATCACCTGAAGTTAGATATTCA TCGCACCTCTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCAGATCACCTGAAGTTAGATATTCA A G APOBEC3G Ensembl:ENSG00000239713 Protein coding intron GSE47997;GSE38233;GSE38233 K562 cells&HepG2 cells;cultured B-cells;cultured B-cells - 23474544,24183664,24183664 RNA-Seq:(High) rs1382001151 Functional Loss SNV dbSNP153 33..33 33 - - - 33561 RMVar_ID_33561 Human_SNP_ID_703911651 A-to-I Human chr22 + 39079913 39079913 39079913 AAAAAAAAAAAAAATTAGCCAGGCATGGTGGCAGTCACCTGTAATCCCAGCTACTCGGGAGGCTG AAAAAAAAAAAAAATTAGCCAGGCATGGTGGCGGTCACCTGTAATCCCAGCTACTCGGGAGGCTG A G APOBEC3G Ensembl:ENSG00000239713 Protein coding intron GSE47997;GSE38233;GSE38233 K562 cells&HepG2 cells;cultured B-cells;cultured B-cells - 23474544,24183664,24183664 RNA-Seq:(High) rs1292175301 Functional Loss SNV dbSNP153 33..33 33 - - - 33562 RMVar_ID_33562 Human_SNP_ID_703911655 A-to-I Human chr22 + 39079917 39079917 39079917 AAAAAAAAAATTAGCCAGGCATGGTGGCAGTCACCTGTAATCCCAGCTACTCGGGAGGCTGAGGC AAAAAAAAAATTAGCCAGGCATGGTGGCAGTCGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGC A G APOBEC3G Ensembl:ENSG00000239713 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1010059326 Functional Loss SNV dbSNP153 33..33 33 - - - 33563 RMVar_ID_33563 Human_SNP_ID_703957938 A-to-I Human chr22 + 39247998 39247998 39247998 GGCTGAGTCAGGAGGGAGAATCCCCTGAGCCCAGGAGTTCAAGACTGCAGTGAGCCATCTCAGAG GGCTGAGTCAGGAGGGAGAATCCCCTGAGCCCGGGAGTTCAAGACTGCAGTGAGCCATCTCAGAG A G AL031590.1 Ensembl:ENSG00000284633 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031741201 Functional Loss SNV dbSNP153 33..33 33 - - - 33564 RMVar_ID_33564 Human_SNP_ID_703992710 A-to-I Human chr22 + 39371669 39371669 39371669 AAAAAATTAACCAGGTATCGTGGCAAACGCCTATAGTCCCGGCTACTCAGGAGGCTGAGGCTGGT AAAAAATTAACCAGGTATCGTGGCAAACGCCTGTAGTCCCGGCTACTCAGGAGGCTGAGGCTGGT A G SYNGR1 Ensembl:ENSG00000100321 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs938785100 Functional Loss SNV dbSNP153 33..33 33 - - - 33565 RMVar_ID_33565 Human_SNP_ID_703995239 A-to-I Human chr22 + 39381049 39381049 39381049 TTAGCCCAGGCTGGTCTTGATCTCCTGGCCTCAAGCAATCCTTCCACCTTGGCCTATCAAAGTTG TTAGCCCAGGCTGGTCTTGATCTCCTGGCCTCGAGCAATCCTTCCACCTTGGCCTATCAAAGTTG A G SYNGR1 Ensembl:ENSG00000100321 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1366064271 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109697,RMVar_hsa_circ_214399,RMVar_hsa_circ_104354,RMVar_hsa_circ_214400 33566 RMVar_ID_33566 Human_SNP_ID_704006484 A-to-I Human chr22 + 39423112 39423112 39423112 CTCCAGCCTTAGCCTCCTGAGTAGCTGGAACTATAGGTGTGTGCCACCACACCTGGCTAATTTTG CTCCAGCCTTAGCCTCCTGAGTAGCTGGAACTGTAGGTGTGTGCCACCACACCTGGCTAATTTTG A G TAB1 Ensembl:ENSG00000100324 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs528187464 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9136,RMVar_hsa_circ_109697,RMVar_hsa_circ_214399,RMVar_hsa_circ_14871,RMVar_hsa_circ_126129,RMVar_hsa_circ_214402,RMVar_hsa_circ_119775,RMVar_hsa_circ_345389,RMVar_hsa_circ_214403 33567 RMVar_ID_33567 Human_SNP_ID_704006854 A-to-I Human chr22 + 39424508 39424508 39424508 GCTCTGTTGGCCAAGCTGGAGTGCAGTGGTGCAATCTCGGCTCACTGTAACCTCCACCTCCCGGG GCTCTGTTGGCCAAGCTGGAGTGCAGTGGTGCGATCTCGGCTCACTGTAACCTCCACCTCCCGGG A G TAB1 Ensembl:ENSG00000100324 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1399171353 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9136,RMVar_hsa_circ_109697,RMVar_hsa_circ_214399,RMVar_hsa_circ_14871,RMVar_hsa_circ_126129,RMVar_hsa_circ_214402,RMVar_hsa_circ_119775,RMVar_hsa_circ_345389,RMVar_hsa_circ_214403 33568 RMVar_ID_33568 Human_SNP_ID_704028261 A-to-I Human chr22 + 39505087 39505087 39505087 ATGGTGGCGCATGCCTTAAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAACCCG ATGGTGGCGCATGCCTTAAGTCCCAGCTACTCCGGAGGCTGAGGCAGGAGAATTGCTTGAACCCG A C MIEF1 Ensembl:ENSG00000100335 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1330601591 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1307991 RMVar_hsa_circ_107542,RMVar_hsa_circ_123436,RMVar_hsa_circ_214407,RMVar_hsa_circ_214408 33569 RMVar_ID_33569 Human_SNP_ID_704036113 A-to-I Human chr22 - 39529288 39529286 39529288 GAAGTCCTGGGGAGGATTTACACACAGACCGGAGCTGGCTTCCGCAGGCCTGGGCAGAGCATCTG GAAGTCCTGGGGAGGATTTACACACAGACCGG__CTGGCTTCCGCAGGCCTGGGCAGAGCATCTG GCT G RPS19BP1 Ensembl:ENSG00000187051 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1489095369 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_580958,Human_RBP_ID_4699110,Human_RBP_ID_5149035,Human_RBP_ID_7083160,Human_RBP_ID_8550712,Human_RBP_ID_22087385,Human_RBP_ID_26500339,Human_RBP_ID_27496106,Human_RBP_ID_27565390 Human_miRNA_ID_3005057 RMVar_hsa_circ_214411,RMVar_hsa_circ_101652 33570 RMVar_ID_33570 Human_SNP_ID_500742308 A-to-I Human chr12 - 50008706 50008706 50008706 GGTCAATCACTTGAGGTCAGGAGTTTGAGACCAGCCTAGCCAACGTGGTGAAACCCCATCTCTAG GGTCAATCACTTGAGGTCAGGAGTTTGAGACCGGCCTAGCCAACGTGGTGAAACCCCATCTCTAG T C RACGAP1 Ensembl:ENSG00000161800 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1019614983 Functional Loss SNV dbSNP153 33..33 33 - - - 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 33571 RMVar_ID_33571 Human_SNP_ID_500742309 A-to-I Human chr12 - 50008706 50008706 50008706 GGTCAATCACTTGAGGTCAGGAGTTTGAGACCAGCCTAGCCAACGTGGTGAAACCCCATCTCTAG GGTCAATCACTTGAGGTCAGGAGTTTGAGACCCGCCTAGCCAACGTGGTGAAACCCCATCTCTAG T G RACGAP1 Ensembl:ENSG00000161800 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1019614983 Functional Loss SNV dbSNP153 33..33 33 - - - 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 33572 RMVar_ID_33572 Human_SNP_ID_500742321 A-to-I Human chr12 - 50008768 50008768 50008768 TATCTTTCGGCCGGGCATGGTGGCTTATGCCTATAATCCTAGCACTTTGGGAGGCTGAGGCAGGT TATCTTTCGGCCGGGCATGGTGGCTTATGCCTGTAATCCTAGCACTTTGGGAGGCTGAGGCAGGT T C RACGAP1 Ensembl:ENSG00000161800 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs991494951 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11959942 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 33573 RMVar_ID_33573 Human_SNP_ID_500742322 A-to-I Human chr12 - 50008784 50008784 50008784 TTGTACATAAAAATAGTATCTTTCGGCCGGGCATGGTGGCTTATGCCTATAATCCTAGCACTTTG TTGTACATAAAAATAGTATCTTTCGGCCGGGCTTGGTGGCTTATGCCTATAATCCTAGCACTTTG T A RACGAP1 Ensembl:ENSG00000161800 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs598144 Functional Loss SNV dbSNP153 33..33 33 - - - 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 33574 RMVar_ID_33574 Human_SNP_ID_500742323 A-to-I Human chr12 - 50008784 50008784 50008784 TTGTACATAAAAATAGTATCTTTCGGCCGGGCATGGTGGCTTATGCCTATAATCCTAGCACTTTG TTGTACATAAAAATAGTATCTTTCGGCCGGGCGTGGTGGCTTATGCCTATAATCCTAGCACTTTG T C RACGAP1 Ensembl:ENSG00000161800 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs598144 Functional Loss SNV dbSNP153 33..33 33 - - - 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 33575 RMVar_ID_33575 Human_SNP_ID_500742324 A-to-I Human chr12 - 50008784 50008784 50008784 TTGTACATAAAAATAGTATCTTTCGGCCGGGCATGGTGGCTTATGCCTATAATCCTAGCACTTTG TTGTACATAAAAATAGTATCTTTCGGCCGGGCCTGGTGGCTTATGCCTATAATCCTAGCACTTTG T G RACGAP1 Ensembl:ENSG00000161800 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs598144 Functional Loss SNV dbSNP153 33..33 33 - - - 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 33576 RMVar_ID_33576 Human_SNP_ID_500742787 A-to-I Human chr12 - 50010748 50010748 50010748 TTGTATTTTTAGTAGAGGTGGGGTTTCTCCATATTGGTCAGGCTGGTCTCGAACTCCCGACCTCA TTGTATTTTTAGTAGAGGTGGGGTTTCTCCATGTTGGTCAGGCTGGTCTCGAACTCCCGACCTCA T C RACGAP1 Ensembl:ENSG00000161800 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1486539383 Functional Loss SNV dbSNP153 33..33 33 - - - 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 33577 RMVar_ID_33577 Human_SNP_ID_500742810 A-to-I Human chr12 - 50010810 50010810 50010810 CTCCTGTCTCAGCCTCCCGAGTAGCTGGAATTACAGGCATGTGCCAACACGCCTGGCTAATTTTG CTCCTGTCTCAGCCTCCCGAGTAGCTGGAATTTCAGGCATGTGCCAACACGCCTGGCTAATTTTG T A RACGAP1 Ensembl:ENSG00000161800 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs572502348 Functional Loss SNV dbSNP153 33..33 33 - - - 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 33578 RMVar_ID_33578 Human_SNP_ID_500743844 A-to-I Human chr12 - 50015253 50015253 50015253 CCTGTATTCCCAGCTACTCAGGAGGCTGAGGCAGAAGAATCACTTGAGGCCAGGAGTTTGAGACC CCTGTATTCCCAGCTACTCAGGAGGCTGAGGCCGAAGAATCACTTGAGGCCAGGAGTTTGAGACC T G RACGAP1 Ensembl:ENSG00000161800 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1479544648 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17561377 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 33579 RMVar_ID_33579 Human_SNP_ID_500743881 A-to-I Human chr12 - 50015482 50015482 50015482 AATTTTTTGTAGAGATAAGGTCTCCCTATTTTACCCAGGCTAGTGTCCAACTCCTGGCCTCAAGC AATTTTTTGTAGAGATAAGGTCTCCCTATTTTGCCCAGGCTAGTGTCCAACTCCTGGCCTCAAGC T C RACGAP1 Ensembl:ENSG00000161800 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1463544994 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11960109 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 33580 RMVar_ID_33580 Human_SNP_ID_500744140 A-to-I Human chr12 - 50016261 50016261 50016261 TCCTTGTCTCAGCCTCTCGAGTAGCAGGGATTACAGACACACGCCACCACGCCCGGCTAATTTTT TCCTTGTCTCAGCCTCTCGAGTAGCAGGGATTGCAGACACACGCCACCACGCCCGGCTAATTTTT T C RACGAP1 Ensembl:ENSG00000161800 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1465109415 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6192254,Human_RBP_ID_11960131 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 33581 RMVar_ID_33581 Human_SNP_ID_500756375 A-to-I Human chr12 + 50067681 50067681 50067681 CCTCAGGTGATCCGCCTGTCTCGGCCTCCCGGAGTGCTGGGATTACAGGCGTGAGCCACTGCGCC CCTCAGGTGATCCGCCTGTCTCGGCCTCCCGGCGTGCTGGGATTACAGGCGTGAGCCACTGCGCC A C ASIC1 Ensembl:ENSG00000110881 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1254032332 Functional Loss SNV dbSNP153 33..33 33 - - - 33582 RMVar_ID_33582 Human_SNP_ID_500762999 A-to-I Human chr12 + 50092759 50092759 50092759 GGGGTCAATTTTAGTTTAAAAGGGAGAAAGCCAGGCACGGTGGCACATTCCTGTAGACCCAGCTA GGGGTCAATTTTAGTTTAAAAGGGAGAAAGCCCGGCACGGTGGCACATTCCTGTAGACCCAGCTA A C SMARCD1 Ensembl:ENSG00000066117 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs563965779 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119043,RMVar_hsa_circ_91325,RMVar_hsa_circ_156401,RMVar_hsa_circ_156402,RMVar_hsa_circ_42747 33583 RMVar_ID_33583 Human_SNP_ID_500763007 A-to-I Human chr12 + 50092791 50092791 50092791 AGGCACGGTGGCACATTCCTGTAGACCCAGCTACTCCAGAGGCTGAGGTGGGTAGATCACTTGAG AGGCACGGTGGCACATTCCTGTAGACCCAGCTGCTCCAGAGGCTGAGGTGGGTAGATCACTTGAG A G SMARCD1 Ensembl:ENSG00000066117 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1293981386 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119043,RMVar_hsa_circ_91325,RMVar_hsa_circ_156401,RMVar_hsa_circ_156402,RMVar_hsa_circ_42747 33584 RMVar_ID_33584 Human_SNP_ID_500763150 A-to-I Human chr12 + 50093318 50093318 50093318 TCAAGCAATTCTCGTGCCTCAGCCTCCCAAGTAGTTGTAATTACAGGCGTGCACCACTTTTTGTA TCAAGCAATTCTCGTGCCTCAGCCTCCCAAGTGGTTGTAATTACAGGCGTGCACCACTTTTTGTA A G SMARCD1 Ensembl:ENSG00000066117 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1275374891 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119043,RMVar_hsa_circ_91325,RMVar_hsa_circ_156401,RMVar_hsa_circ_156402,RMVar_hsa_circ_42747 33585 RMVar_ID_33585 Human_SNP_ID_500770013 A-to-I Human chr12 + 50118176 50118175 50118176 TCAAGCAGTTCTCCTGCCTTAGCCTCTCGAGTAGCTGGGATTACAGGCATGCGCCACCACGCCCA TCAAGCAGTTCTCCTGCCTTAGCCTCTCGAGT_GCTGGGATTACAGGCATGCGCCACCACGCCCA TA T AC074032.1,COX14 Ensembl:ENSG00000272368,Ensembl:ENSG00000178449 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388563237 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_8377730 RMVar_hsa_circ_123401,RMVar_hsa_circ_156406 33586 RMVar_ID_33586 Human_SNP_ID_500770350 A-to-I Human chr12 + 50119573 50119573 50119573 AAAAACTGGGCGGTGTGGTGGTACACACCTGTAGCGTCAGCTACTTGGGAGGCTGAGGTGGGAGG AAAAACTGGGCGGTGTGGTGGTACACACCTGTGGCGTCAGCTACTTGGGAGGCTGAGGTGGGAGG A G AC074032.1,COX14 Ensembl:ENSG00000272368,Ensembl:ENSG00000178449 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1328772649 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123401,RMVar_hsa_circ_156406 33587 RMVar_ID_33587 Human_SNP_ID_500770476 A-to-I Human chr12 + 50120071 50120071 50120071 ACAAGATGCCAACTGGCAAGCAGCTAGCTGACATTGGCTATAAGACCTTCTCTACCTCCATGATG ACAAGATGCCAACTGGCAAGCAGCTAGCTGACGTTGGCTATAAGACCTTCTCTACCTCCATGATG A G AC074032.1,COX14 Ensembl:ENSG00000272368,Ensembl:ENSG00000178449 lincRNA,Protein coding intron,CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1565753819 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1472974,Human_RBP_ID_5558231,Human_RBP_ID_6242686,Human_RBP_ID_26805638 Human_Splice_Rec_1367822,Human_Splice_Rec_1367826,Human_Splice_Rec_1367828,Human_Splice_Rec_1367830 Human_miRNA_ID_2668180,Human_miRNA_ID_2727917 RMVar_hsa_circ_103065,RMVar_hsa_circ_123401,RMVar_hsa_circ_156406,RMVar_hsa_circ_156407 33588 RMVar_ID_33588 Human_SNP_ID_500771419 A-to-I Human chr12 + 50123814 50123814 50123814 GCCTCACCCTCCTGAGTAGCTGGGCTACAGGCACATACCACCACACCTGGCTACTTTTATTATTT GCCTCACCCTCCTGAGTAGCTGGGCTACAGGCTCATACCACCACACCTGGCTACTTTTATTATTT A T AC074032.1 Ensembl:ENSG00000272368 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs577234946 Functional Loss SNV dbSNP153 33..33 33 - - - 33589 RMVar_ID_33589 Human_SNP_ID_500772247 A-to-I Human chr12 + 50127495 50127495 50127495 ACTTCAAACTCCTGAGCTCAAGTCATCCTCCCACCTGATTCTCCAGAGTAGCTGGGACTACAGGT ACTTCAAACTCCTGAGCTCAAGTCATCCTCCCGCCTGATTCTCCAGAGTAGCTGGGACTACAGGT A G AC074032.1 Ensembl:ENSG00000272368 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1190261528 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5246441,Human_RBP_ID_11961459 33590 RMVar_ID_33590 Human_SNP_ID_500775529 A-to-I Human chr12 - 50139621 50139621 50139621 GCCCAGCTAATTTTTGTATTTTTGGTAGAGACAGATTTTCATCATGTTGCCGGGCTAATCTTGAA GCCCAGCTAATTTTTGTATTTTTGGTAGAGACCGATTTTCATCATGTTGCCGGGCTAATCTTGAA T G CERS5 Ensembl:ENSG00000139624 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs900516977 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27751,RMVar_hsa_circ_124242,RMVar_hsa_circ_121543,RMVar_hsa_circ_89003,RMVar_hsa_circ_26756,RMVar_hsa_circ_156413,RMVar_hsa_circ_156414,RMVar_hsa_circ_156412,RMVar_hsa_circ_156415,RMVar_hsa_circ_357610,RMVar_hsa_circ_330942,RMVar_hsa_circ_156418,RMVar_hsa_circ_341758,RMVar_hsa_circ_156419 33591 RMVar_ID_33591 Human_SNP_ID_500777698 A-to-I Human chr12 - 50148534 50148534 50148534 GGAGTGCAGTGGTGAGATCTCAGCTCACTGCAACCTCTGTCTCCCGAGTTCAAGAGATCCTCTCA GGAGTGCAGTGGTGAGATCTCAGCTCACTGCACCCTCTGTCTCCCGAGTTCAAGAGATCCTCTCA T G CERS5 Ensembl:ENSG00000139624 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1174756892 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8377764,Human_RBP_ID_11961847 Human_Splice_Rec_1368054,Human_Splice_Rec_1368055 RMVar_hsa_circ_124242,RMVar_hsa_circ_156414 33592 RMVar_ID_33592 Human_SNP_ID_500777751 A-to-I Human chr12 - 50148735 50148735 50148735 ATGCCCGGCTAATTTTTTGTTGTTGTATTTTTAGTAGAAGATGGCATTTCGCCATGTTGGCCAGG ATGCCCGGCTAATTTTTTGTTGTTGTATTTTTGGTAGAAGATGGCATTTCGCCATGTTGGCCAGG T C CERS5 Ensembl:ENSG00000139624 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs750083165 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11961856 RMVar_hsa_circ_124242,RMVar_hsa_circ_156414 33593 RMVar_ID_33593 Human_SNP_ID_500778608 A-to-I Human chr12 - 50151912 50151912 50151912 GCCGCGCACGGCGACTCACGCCTGTAATCCCAACACTTTGGGAGGCCGAGGTGGGTGAATCCACT GCCGCGCACGGCGACTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGTGAATCCACT T C CERS5 Ensembl:ENSG00000139624 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs974709293 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124242,RMVar_hsa_circ_156414 33594 RMVar_ID_33594 Human_SNP_ID_500778609 A-to-I Human chr12 - 50151912 50151912 50151912 GCCGCGCACGGCGACTCACGCCTGTAATCCCAACACTTTGGGAGGCCGAGGTGGGTGAATCCACT GCCGCGCACGGCGACTCACGCCTGTAATCCCACCACTTTGGGAGGCCGAGGTGGGTGAATCCACT T G CERS5 Ensembl:ENSG00000139624 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs974709293 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124242,RMVar_hsa_circ_156414 33595 RMVar_ID_33595 Human_SNP_ID_500778729 A-to-I Human chr12 - 50152507 50152507 50152507 GAACTCCTGACCTCAAGTGATCCGCTTGCCTCAGCCTCCTAAAGTGCTGGGATTACAGGCATAAG GAACTCCTGACCTCAAGTGATCCGCTTGCCTCTGCCTCCTAAAGTGCTGGGATTACAGGCATAAG T A CERS5 Ensembl:ENSG00000139624 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1220693893 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124242,RMVar_hsa_circ_156414 33596 RMVar_ID_33596 Human_SNP_ID_500779090 A-to-I Human chr12 - 50153870 50153870 50153870 AGCTCACTGCAACCTCTGCCTCCCAGGTTCAAATGATTCTCCTGCCTCAGCCTTCCAAGTAGCTG AGCTCACTGCAACCTCTGCCTCCCAGGTTCAATTGATTCTCCTGCCTCAGCCTTCCAAGTAGCTG T A CERS5 Ensembl:ENSG00000139624 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1015762622 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1368048,Human_Splice_Rec_1368049 RMVar_hsa_circ_124242,RMVar_hsa_circ_156414 33597 RMVar_ID_33597 Human_SNP_ID_500779091 A-to-I Human chr12 - 50153870 50153870 50153870 AGCTCACTGCAACCTCTGCCTCCCAGGTTCAAATGATTCTCCTGCCTCAGCCTTCCAAGTAGCTG AGCTCACTGCAACCTCTGCCTCCCAGGTTCAAGTGATTCTCCTGCCTCAGCCTTCCAAGTAGCTG T C CERS5 Ensembl:ENSG00000139624 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1015762622 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1368048,Human_Splice_Rec_1368049 RMVar_hsa_circ_124242,RMVar_hsa_circ_156414 33598 RMVar_ID_33598 Human_SNP_ID_500779094 A-to-I Human chr12 - 50153878 50153878 50153878 GCAGTCACAGCTCACTGCAACCTCTGCCTCCCAGGTTCAAATGATTCTCCTGCCTCAGCCTTCCA GCAGTCACAGCTCACTGCAACCTCTGCCTCCCGGGTTCAAATGATTCTCCTGCCTCAGCCTTCCA T C CERS5 Ensembl:ENSG00000139624 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1220987160 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1368048,Human_Splice_Rec_1368049 RMVar_hsa_circ_124242,RMVar_hsa_circ_156414 33599 RMVar_ID_33599 Human_SNP_ID_500779338 A-to-I Human chr12 - 50154986 50154986 50154986 AGGCATGGTGGTGCACGCCTATAGTCCCAGCTACTTGGGCAGCTGAGGCAGGAGAATCACTTGAA AGGCATGGTGGTGCACGCCTATAGTCCCAGCTGCTTGGGCAGCTGAGGCAGGAGAATCACTTGAA T C CERS5 Ensembl:ENSG00000139624 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1308232035 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124242,RMVar_hsa_circ_156414 33600 RMVar_ID_33600 Human_SNP_ID_500779903 A-to-I Human chr12 - 50156535 50156535 50156535 GCTGGAATGCAATGGCATGATCATGACTCACTACAGCCTCCACCTCTTGGCTCAAACAATCCTCC GCTGGAATGCAATGGCATGATCATGACTCACTGCAGCCTCCACCTCTTGGCTCAAACAATCCTCC T C CERS5 Ensembl:ENSG00000139624 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941304395 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11962035 RMVar_hsa_circ_124242,RMVar_hsa_circ_156414 33601 RMVar_ID_33601 Human_SNP_ID_500779907 A-to-I Human chr12 - 50156556 50156556 50156556 AAGCTTCACTCTGTCAGCCACGCTGGAATGCAATGGCATGATCATGACTCACTACAGCCTCCACC AAGCTTCACTCTGTCAGCCACGCTGGAATGCAGTGGCATGATCATGACTCACTACAGCCTCCACC T C CERS5 Ensembl:ENSG00000139624 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs994229161 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11962035 RMVar_hsa_circ_124242,RMVar_hsa_circ_156414 33602 RMVar_ID_33602 Human_SNP_ID_500781131 A-to-I Human chr12 - 50162003 50162003 50162003 GGGTGTGGTGGCATGCGCCTTAAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAA GGGTGTGGTGGCATGCGCCTTAAGTCCCAGCTCCTTGGGAGGCTGAGGCAGGAGAATCGCTTGAA T G CERS5 Ensembl:ENSG00000139624 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs867761728 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124242,RMVar_hsa_circ_156414 33603 RMVar_ID_33603 Human_SNP_ID_500781138 A-to-I Human chr12 - 50162039 50162039 50162039 AAACCCTGTCTTTACTAAAAATACAAGAAATTAGCTGGGTGTGGTGGCATGCGCCTTAAGTCCCA AAACCCTGTCTTTACTAAAAATACAAGAAATTGGCTGGGTGTGGTGGCATGCGCCTTAAGTCCCA T C CERS5 Ensembl:ENSG00000139624 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1156662697 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124242,RMVar_hsa_circ_156414 33604 RMVar_ID_33604 Human_SNP_ID_500781497 A-to-I Human chr12 - 50163477 50163477 50163477 ATATCGGGGCATGGCCTTGCATGCTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGC ATATCGGGGCATGGCCTTGCATGCTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGC T C CERS5 Ensembl:ENSG00000139624 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1418952275 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124242,RMVar_hsa_circ_156414 33605 RMVar_ID_33605 Human_SNP_ID_500790252 A-to-I Human chr12 - 50194577 50194577 50194577 TATATGTTGCTGGGCCAGGCGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCTAAGT TATATGTTGCTGGGCCAGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCTAAGT T C LIMA1 Ensembl:ENSG00000050405 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs573215140 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5462,RMVar_hsa_circ_267719,RMVar_hsa_circ_364724,RMVar_hsa_circ_376857,RMVar_hsa_circ_334061,RMVar_hsa_circ_361218,RMVar_hsa_circ_313075 33606 RMVar_ID_33606 Human_SNP_ID_500791865 A-to-I Human chr12 - 50201671 50201671 50201671 GCTGGTCTTGAACTCCTGACCTCAGGCGATCCACCCGCCTCAGCTTCCCAAAGTGCTGGGATTAC GCTGGTCTTGAACTCCTGACCTCAGGCGATCCGCCCGCCTCAGCTTCCCAAAGTGCTGGGATTAC T C LIMA1 Ensembl:ENSG00000050405 Protein coding 5'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs937255680 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267719,RMVar_hsa_circ_364724,RMVar_hsa_circ_376857,RMVar_hsa_circ_313075,RMVar_hsa_circ_264925,RMVar_hsa_circ_345531 33607 RMVar_ID_33607 Human_SNP_ID_500791866 A-to-I Human chr12 - 50201671 50201671 50201671 GCTGGTCTTGAACTCCTGACCTCAGGCGATCCACCCGCCTCAGCTTCCCAAAGTGCTGGGATTAC GCTGGTCTTGAACTCCTGACCTCAGGCGATCCCCCCGCCTCAGCTTCCCAAAGTGCTGGGATTAC T G LIMA1 Ensembl:ENSG00000050405 Protein coding 5'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs937255680 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267719,RMVar_hsa_circ_364724,RMVar_hsa_circ_376857,RMVar_hsa_circ_313075,RMVar_hsa_circ_264925,RMVar_hsa_circ_345531 33608 RMVar_ID_33608 Human_SNP_ID_500791894 A-to-I Human chr12 - 50201773 50201773 50201773 CTGCCTCAGCCTCCCAAGTAACTGGGATTACAAGTGTGCACCACCACACGTGGCTAATTTTTTGT CTGCCTCAGCCTCCCAAGTAACTGGGATTACAGGTGTGCACCACCACACGTGGCTAATTTTTTGT T C LIMA1 Ensembl:ENSG00000050405 Protein coding 5'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1405983603 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267719,RMVar_hsa_circ_364724,RMVar_hsa_circ_376857,RMVar_hsa_circ_313075,RMVar_hsa_circ_264925,RMVar_hsa_circ_345531 33609 RMVar_ID_33609 Human_SNP_ID_500792246 A-to-I Human chr12 - 50203246 50203246 50203246 CTTTGGGAGCCTGAGGTGGGTGGGTCATTTGAAGTCAGGAGTTCAGAACCAGCCTGGCCAACATG CTTTGGGAGCCTGAGGTGGGTGGGTCATTTGAGGTCAGGAGTTCAGAACCAGCCTGGCCAACATG T C LIMA1 Ensembl:ENSG00000050405 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1272779699 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267719,RMVar_hsa_circ_364724,RMVar_hsa_circ_376857,RMVar_hsa_circ_313075,RMVar_hsa_circ_264925,RMVar_hsa_circ_345531 33610 RMVar_ID_33610 Human_SNP_ID_500792247 A-to-I Human chr12 - 50203246 50203246 50203246 CTTTGGGAGCCTGAGGTGGGTGGGTCATTTGAAGTCAGGAGTTCAGAACCAGCCTGGCCAACATG CTTTGGGAGCCTGAGGTGGGTGGGTCATTTGACGTCAGGAGTTCAGAACCAGCCTGGCCAACATG T G LIMA1 Ensembl:ENSG00000050405 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1272779699 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267719,RMVar_hsa_circ_364724,RMVar_hsa_circ_376857,RMVar_hsa_circ_313075,RMVar_hsa_circ_264925,RMVar_hsa_circ_345531 33611 RMVar_ID_33611 Human_SNP_ID_500793805 A-to-I Human chr12 - 50209817 50209817 50209817 CTCTACCAAAAACTCAAATAATTAGGTGTGGTAGCAGACGCCTGTAATCCCAGCTACTCTGGAGG CTCTACCAAAAACTCAAATAATTAGGTGTGGTTGCAGACGCCTGTAATCCCAGCTACTCTGGAGG T A LIMA1 Ensembl:ENSG00000050405 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1186695411 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267719,RMVar_hsa_circ_376857,RMVar_hsa_circ_56365,RMVar_hsa_circ_264925,RMVar_hsa_circ_156425,RMVar_hsa_circ_288627 33612 RMVar_ID_33612 Human_SNP_ID_500795261 A-to-I Human chr12 - 50215925 50215925 50215925 CTGCCTCAGCCTCCTGAGTAGCTGGGATTACAAGTGTGCACCACGAAGTCCGGCTAATTTTTGTA CTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGTGTGCACCACGAAGTCCGGCTAATTTTTGTA T C LIMA1 Ensembl:ENSG00000050405 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs906891211 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267719,RMVar_hsa_circ_376857,RMVar_hsa_circ_56365,RMVar_hsa_circ_264925,RMVar_hsa_circ_156425,RMVar_hsa_circ_288627 33613 RMVar_ID_33613 Human_SNP_ID_500795262 A-to-I Human chr12 - 50215925 50215925 50215925 CTGCCTCAGCCTCCTGAGTAGCTGGGATTACAAGTGTGCACCACGAAGTCCGGCTAATTTTTGTA CTGCCTCAGCCTCCTGAGTAGCTGGGATTACACGTGTGCACCACGAAGTCCGGCTAATTTTTGTA T G LIMA1 Ensembl:ENSG00000050405 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs906891211 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267719,RMVar_hsa_circ_376857,RMVar_hsa_circ_56365,RMVar_hsa_circ_264925,RMVar_hsa_circ_156425,RMVar_hsa_circ_288627 33614 RMVar_ID_33614 Human_SNP_ID_500809045 A-to-I Human chr12 - 50274506 50274506 50274506 ACGATCTTGACTCACTGCAACCTCCAACTCCCAGGTTCAAGAGTCTCCTGCTTCAGCCTCCCAAG ACGATCTTGACTCACTGCAACCTCCAACTCCCGGGTTCAAGAGTCTCCTGCTTCAGCCTCCCAAG T C LIMA1 Ensembl:ENSG00000050405 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1215332608 Functional Loss SNV dbSNP153 33..33 33 - - - 33615 RMVar_ID_33615 Human_SNP_ID_500813701 A-to-I Human chr12 + 50295734 50295734 50295734 CTCACTGCAGCCTCAACTACCCAGACTCAAGCAATCCTCCTACCTCAGCCCGCCAAGTAACTGGG CTCACTGCAGCCTCAACTACCCAGACTCAAGCCATCCTCCTACCTCAGCCCGCCAAGTAACTGGG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941694482 Functional Loss SNV dbSNP153 33..33 33 - - - 33616 RMVar_ID_33616 Human_SNP_ID_500813704 A-to-I Human chr12 + 50295743 50295743 50295743 GCCTCAACTACCCAGACTCAAGCAATCCTCCTACCTCAGCCCGCCAAGTAACTGGGACTACTGGT GCCTCAACTACCCAGACTCAAGCAATCCTCCTGCCTCAGCCCGCCAAGTAACTGGGACTACTGGT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037809976 Functional Loss SNV dbSNP153 33..33 33 - - - 33617 RMVar_ID_33617 Human_SNP_ID_500815350 A-to-I Human chr12 + 50302240 50302240 50302240 ATGCTCCACTGCAGCCTCAACCTGCTGGGCTCAAGCAGTCCTCCCCCTTCAGACTCTCGTGTGGC ATGCTCCACTGCAGCCTCAACCTGCTGGGCTCCAGCAGTCCTCCCCCTTCAGACTCTCGTGTGGC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs533096980 Functional Loss SNV dbSNP153 33..33 33 - - - 33618 RMVar_ID_33618 Human_SNP_ID_500815733 A-to-I Human chr12 + 50303780 50303780 50303780 TACCACCACACCAAGCTAATTTTTGTGTTTTTAGTAGAGATGGTTTCGCCGTGTTGGCCAGGCTG TACCACCACACCAAGCTAATTTTTGTGTTTTTGGTAGAGATGGTTTCGCCGTGTTGGCCAGGCTG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1565872819 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11962701,Human_RBP_ID_23562949 33619 RMVar_ID_33619 Human_SNP_ID_500816106 A-to-I Human chr12 + 50305273 50305272 50305273 CCCGCTACTCAGGAGGTTTAGGCAGGAGAATCACTTGAACCCGAGAGGCAGAGGTTACAGTAGTG CCCGCTACTCAGGAGGTTTAGGCAGGAGAATC_CTTGAACCCGAGAGGCAGAGGTTACAGTAGTG CA C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1307464587 Functional Loss DEL dbSNP153 33..33 33 - - - 33620 RMVar_ID_33620 Human_SNP_ID_500816108 A-to-I Human chr12 + 50305273 50305273 50305273 CCCGCTACTCAGGAGGTTTAGGCAGGAGAATCACTTGAACCCGAGAGGCAGAGGTTACAGTAGTG CCCGCTACTCAGGAGGTTTAGGCAGGAGAATCGCTTGAACCCGAGAGGCAGAGGTTACAGTAGTG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs940788480 Functional Loss SNV dbSNP153 33..33 33 - - - 33621 RMVar_ID_33621 Human_SNP_ID_500817645 A-to-I Human chr12 + 50311317 50311317 50311317 CCTGTAGTCCCAGCTACTCAGAAGGCTGAGGCAGAGAATTGCTTGAACCCGGGAGGTGGAGGTTG CCTGTAGTCCCAGCTACTCAGAAGGCTGAGGCGGAGAATTGCTTGAACCCGGGAGGTGGAGGTTG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1276624856 Functional Loss SNV dbSNP153 33..33 33 - - - 33622 RMVar_ID_33622 Human_SNP_ID_500819327 A-to-I Human chr12 + 50318040 50318040 50318040 GTTGGCCAGGCTGGTCTCCAACTCCGGACCTCAGGTGATTTGTCTGCCTCGGCCTCCAAAATTGC GTTGGCCAGGCTGGTCTCCAACTCCGGACCTCGGGTGATTTGTCTGCCTCGGCCTCCAAAATTGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1331016758 Functional Loss SNV dbSNP153 33..33 33 - - - 33623 RMVar_ID_33623 Human_SNP_ID_500842979 A-to-I Human chr12 + 50409620 50409620 50409620 CCATCTCTACCAAAAAATATACAAAAAAAATTAGGCGGGTATAGTGGCACATGCCTGTAAGGGGC CCATCTCTACCAAAAAATATACAAAAAAAATTCGGCGGGTATAGTGGCACATGCCTGTAAGGGGC A C LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs976138551 Functional Loss SNV dbSNP153 33..33 33 - - - 33624 RMVar_ID_33624 Human_SNP_ID_500842980 A-to-I Human chr12 + 50409620 50409620 50409620 CCATCTCTACCAAAAAATATACAAAAAAAATTAGGCGGGTATAGTGGCACATGCCTGTAAGGGGC CCATCTCTACCAAAAAATATACAAAAAAAATTGGGCGGGTATAGTGGCACATGCCTGTAAGGGGC A G LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs976138551 Functional Loss SNV dbSNP153 33..33 33 - - - 33625 RMVar_ID_33625 Human_SNP_ID_500843158 A-to-I Human chr12 + 50410274 50410274 50410274 ATACCTTTTTTTAATAGAGACAGGGTCTTGCTATGTTGGCTAGGCTGGTTTGAACTCCTGGCCTC ATACCTTTTTTTAATAGAGACAGGGTCTTGCTGTGTTGGCTAGGCTGGTTTGAACTCCTGGCCTC A G LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232227272 Functional Loss SNV dbSNP153 33..33 33 - - - 33626 RMVar_ID_33626 Human_SNP_ID_500843159 A-to-I Human chr12 + 50410283 50410283 50410283 TTTAATAGAGACAGGGTCTTGCTATGTTGGCTAGGCTGGTTTGAACTCCTGGCCTCAAACGATCC TTTAATAGAGACAGGGTCTTGCTATGTTGGCTGGGCTGGTTTGAACTCCTGGCCTCAAACGATCC A G LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878903892 Functional Loss SNV dbSNP153 33..33 33 - - - 33627 RMVar_ID_33627 Human_SNP_ID_500843169 A-to-I Human chr12 + 50410320 50410320 50410320 GGTTTGAACTCCTGGCCTCAAACGATCCTCCCATCTTGGCCTCCCAAAGTGCTGCGATTACAGGT GGTTTGAACTCCTGGCCTCAAACGATCCTCCCGTCTTGGCCTCCCAAAGTGCTGCGATTACAGGT A G LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1391445931 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11963041 33628 RMVar_ID_33628 Human_SNP_ID_500844157 A-to-I Human chr12 + 50414492 50414491 50414493 TGCCTGGCTAATTCTTGTGATTTTGTAAAGACAGGGTTTCACTGTGTTGCCCAGGCTGATCTTGA TGCCTGGCTAATTCTTGTGATTTTGTAAAGAC__GGTTTCACTGTGTTGCCCAGGCTGATCTTGA CAG C LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs750547588 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_156426,RMVar_hsa_circ_156430,RMVar_hsa_circ_324306,RMVar_hsa_circ_337951,RMVar_hsa_circ_368510,RMVar_hsa_circ_373064,RMVar_hsa_circ_357394,RMVar_hsa_circ_325026,RMVar_hsa_circ_308995,RMVar_hsa_circ_313846,RMVar_hsa_circ_83306,RMVar_hsa_circ_156428,RMVar_hsa_circ_156429,RMVar_hsa_circ_156427 33629 RMVar_ID_33629 Human_SNP_ID_500844158 A-to-I Human chr12 + 50414492 50414492 50414492 TGCCTGGCTAATTCTTGTGATTTTGTAAAGACAGGGTTTCACTGTGTTGCCCAGGCTGATCTTGA TGCCTGGCTAATTCTTGTGATTTTGTAAAGACGGGGTTTCACTGTGTTGCCCAGGCTGATCTTGA A G LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1020700493 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_156426,RMVar_hsa_circ_156430,RMVar_hsa_circ_324306,RMVar_hsa_circ_337951,RMVar_hsa_circ_368510,RMVar_hsa_circ_373064,RMVar_hsa_circ_357394,RMVar_hsa_circ_325026,RMVar_hsa_circ_308995,RMVar_hsa_circ_313846,RMVar_hsa_circ_83306,RMVar_hsa_circ_156428,RMVar_hsa_circ_156429,RMVar_hsa_circ_156427 33630 RMVar_ID_33630 Human_SNP_ID_500844474 A-to-I Human chr12 + 50415728 50415728 50415728 GTTTTTTTTTTTTGAGACGGGCTCACTTTGTTACCCCGGCTGGAGTGCGGTGTCACGATCTCGGC GTTTTTTTTTTTTGAGACGGGCTCACTTTGTTTCCCCGGCTGGAGTGCGGTGTCACGATCTCGGC A T LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1311106843 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1368566 RMVar_hsa_circ_156426,RMVar_hsa_circ_156430,RMVar_hsa_circ_324306,RMVar_hsa_circ_337951,RMVar_hsa_circ_368510,RMVar_hsa_circ_373064,RMVar_hsa_circ_357394,RMVar_hsa_circ_325026,RMVar_hsa_circ_308995,RMVar_hsa_circ_313846,RMVar_hsa_circ_83306,RMVar_hsa_circ_156428,RMVar_hsa_circ_156429,RMVar_hsa_circ_156427 33631 RMVar_ID_33631 Human_SNP_ID_500844497 A-to-I Human chr12 + 50415782 50415782 50415782 ACGATCTCGGCTCACTGTAACCTCCACCTCCCAGGTTCAAGCATTCCTCCTGTCTCAGCTCTCCA ACGATCTCGGCTCACTGTAACCTCCACCTCCCGGGTTCAAGCATTCCTCCTGTCTCAGCTCTCCA A G LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs139571560 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1368566,Human_Splice_Rec_1368567 RMVar_hsa_circ_156426,RMVar_hsa_circ_156430,RMVar_hsa_circ_324306,RMVar_hsa_circ_337951,RMVar_hsa_circ_368510,RMVar_hsa_circ_373064,RMVar_hsa_circ_357394,RMVar_hsa_circ_325026,RMVar_hsa_circ_308995,RMVar_hsa_circ_313846,RMVar_hsa_circ_83306,RMVar_hsa_circ_156428,RMVar_hsa_circ_156429,RMVar_hsa_circ_156427 33632 RMVar_ID_33632 Human_SNP_ID_500845038 A-to-I Human chr12 + 50417978 50417978 50417978 CGCCTCCTGGATTCAAGCGATTCGCCTGCCTCAGCCTCCCAAGTACCTGGGATTACAGGCACCCA CGCCTCCTGGATTCAAGCGATTCGCCTGCCTCGGCCTCCCAAGTACCTGGGATTACAGGCACCCA A G LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs950834359 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22547,RMVar_hsa_circ_156426,RMVar_hsa_circ_156430,RMVar_hsa_circ_324306,RMVar_hsa_circ_337951,RMVar_hsa_circ_368510,RMVar_hsa_circ_373064,RMVar_hsa_circ_357394,RMVar_hsa_circ_325026,RMVar_hsa_circ_308995,RMVar_hsa_circ_313846,RMVar_hsa_circ_83306,RMVar_hsa_circ_156428,RMVar_hsa_circ_156429,RMVar_hsa_circ_156427,RMVar_hsa_circ_52618,RMVar_hsa_circ_70091,RMVar_hsa_circ_357249,RMVar_hsa_circ_42391 33633 RMVar_ID_33633 Human_SNP_ID_500845430 A-to-I Human chr12 + 50419705 50419704 50419705 AAGGTGAGATGATCGTTTGAGGCCAGGAGTTCAAGACTGGCTAGACAACATAGCCACACCCCATC AAGGTGAGATGATCGTTTGAGGCCAGGAGTTC_AGACTGGCTAGACAACATAGCCACACCCCATC CA C LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1311028654 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_22547,RMVar_hsa_circ_156426,RMVar_hsa_circ_156430,RMVar_hsa_circ_324306,RMVar_hsa_circ_337951,RMVar_hsa_circ_368510,RMVar_hsa_circ_373064,RMVar_hsa_circ_357394,RMVar_hsa_circ_325026,RMVar_hsa_circ_308995,RMVar_hsa_circ_313846,RMVar_hsa_circ_83306,RMVar_hsa_circ_156428,RMVar_hsa_circ_156429,RMVar_hsa_circ_156427,RMVar_hsa_circ_52618,RMVar_hsa_circ_70091,RMVar_hsa_circ_357249,RMVar_hsa_circ_42391 33634 RMVar_ID_33634 Human_SNP_ID_500845432 A-to-I Human chr12 + 50419715 50419715 50419715 GATCGTTTGAGGCCAGGAGTTCAAGACTGGCTAGACAACATAGCCACACCCCATCTCTACAAAAA GATCGTTTGAGGCCAGGAGTTCAAGACTGGCTGGACAACATAGCCACACCCCATCTCTACAAAAA A G LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1455176064 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22547,RMVar_hsa_circ_156426,RMVar_hsa_circ_156430,RMVar_hsa_circ_324306,RMVar_hsa_circ_337951,RMVar_hsa_circ_368510,RMVar_hsa_circ_373064,RMVar_hsa_circ_357394,RMVar_hsa_circ_325026,RMVar_hsa_circ_308995,RMVar_hsa_circ_313846,RMVar_hsa_circ_83306,RMVar_hsa_circ_156428,RMVar_hsa_circ_156429,RMVar_hsa_circ_156427,RMVar_hsa_circ_52618,RMVar_hsa_circ_70091,RMVar_hsa_circ_357249,RMVar_hsa_circ_42391 33635 RMVar_ID_33635 Human_SNP_ID_500846564 A-to-I Human chr12 + 50423956 50423956 50423956 TTTGTATTGTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTCATCTTGAACTCCTGACCT TTTGTATTGTTTAGTAGAGACAGGGTTTCACCGTGTTGGCCAGGCTCATCTTGAACTCCTGACCT A G LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs980267651 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22547,RMVar_hsa_circ_156426,RMVar_hsa_circ_156430,RMVar_hsa_circ_324306,RMVar_hsa_circ_368510,RMVar_hsa_circ_373064,RMVar_hsa_circ_357394,RMVar_hsa_circ_325026,RMVar_hsa_circ_308995,RMVar_hsa_circ_313846,RMVar_hsa_circ_83306,RMVar_hsa_circ_156428,RMVar_hsa_circ_156429,RMVar_hsa_circ_156427,RMVar_hsa_circ_52618,RMVar_hsa_circ_70091,RMVar_hsa_circ_357249,RMVar_hsa_circ_42391 33636 RMVar_ID_33636 Human_SNP_ID_500846624 A-to-I Human chr12 + 50424231 50424231 50424231 ACTCTGCCAAATTTTTTTTTAATTAGTGGAGCATGGTGTTCCAGGCCTGTAGTCCTAGCTACTCA ACTCTGCCAAATTTTTTTTTAATTAGTGGAGCGTGGTGTTCCAGGCCTGTAGTCCTAGCTACTCA A G LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs975535794 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11963339 RMVar_hsa_circ_22547,RMVar_hsa_circ_156426,RMVar_hsa_circ_156430,RMVar_hsa_circ_324306,RMVar_hsa_circ_368510,RMVar_hsa_circ_373064,RMVar_hsa_circ_357394,RMVar_hsa_circ_325026,RMVar_hsa_circ_308995,RMVar_hsa_circ_313846,RMVar_hsa_circ_83306,RMVar_hsa_circ_156428,RMVar_hsa_circ_156429,RMVar_hsa_circ_156427,RMVar_hsa_circ_52618,RMVar_hsa_circ_70091,RMVar_hsa_circ_357249,RMVar_hsa_circ_42391 33637 RMVar_ID_33637 Human_SNP_ID_500846641 A-to-I Human chr12 + 50424309 50424309 50424309 AGAGCATCATTTGAACCCCGGAGTTTGAGGCTACAGTGAGCTATGGGCACGCCACTGCACTCCAG AGAGCATCATTTGAACCCCGGAGTTTGAGGCTGCAGTGAGCTATGGGCACGCCACTGCACTCCAG A G LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1360062543 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11963340 RMVar_hsa_circ_22547,RMVar_hsa_circ_156426,RMVar_hsa_circ_156430,RMVar_hsa_circ_324306,RMVar_hsa_circ_368510,RMVar_hsa_circ_373064,RMVar_hsa_circ_357394,RMVar_hsa_circ_325026,RMVar_hsa_circ_308995,RMVar_hsa_circ_313846,RMVar_hsa_circ_83306,RMVar_hsa_circ_156428,RMVar_hsa_circ_156429,RMVar_hsa_circ_156427,RMVar_hsa_circ_52618,RMVar_hsa_circ_70091,RMVar_hsa_circ_357249,RMVar_hsa_circ_42391 33638 RMVar_ID_33638 Human_SNP_ID_500848534 A-to-I Human chr12 + 50431103 50431103 50431103 CTGCCTGACCAACATGGAGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCGGGGCATGGTGG CTGCCTGACCAACATGGAGAAACCCCGTCTCTTCTAAAAATACAAAAATTAGCGGGGCATGGTGG A T LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1007834826 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22547,RMVar_hsa_circ_156430,RMVar_hsa_circ_324306,RMVar_hsa_circ_368510,RMVar_hsa_circ_373064,RMVar_hsa_circ_325026,RMVar_hsa_circ_313846,RMVar_hsa_circ_156428,RMVar_hsa_circ_156429,RMVar_hsa_circ_52618,RMVar_hsa_circ_42391,RMVar_hsa_circ_270678,RMVar_hsa_circ_281157,RMVar_hsa_circ_300058,RMVar_hsa_circ_331199,RMVar_hsa_circ_362825,RMVar_hsa_circ_320194,RMVar_hsa_circ_282759,RMVar_hsa_circ_278339,RMVar_hsa_circ_275327,RMVar_hsa_circ_65767,RMVar_hsa_circ_156433,RMVar_hsa_circ_156435,RMVar_hsa_circ_156436,RMVar_hsa_circ_156434,RMVar_hsa_circ_312274,RMVar_hsa_circ_156431,RMVar_hsa_circ_156432,RMVar_hsa_circ_327428,RMVar_hsa_circ_350740,RMVar_hsa_circ_296643,RMVar_hsa_circ_284685,RMVar_hsa_circ_156441,RMVar_hsa_circ_156442,RMVar_hsa_circ_65030,RMVar_hsa_circ_42887,RMVar_hsa_circ_290610,RMVar_hsa_circ_305837,RMVar_hsa_circ_350297,RMVar_hsa_circ_310910,RMVar_hsa_circ_364298,RMVar_hsa_circ_340771,RMVar_hsa_circ_294181,RMVar_hsa_circ_273923,RMVar_hsa_circ_288347,RMVar_hsa_circ_271324,RMVar_hsa_circ_156446,RMVar_hsa_circ_156448,RMVar_hsa_circ_156449,RMVar_hsa_circ_156447,RMVar_hsa_circ_156444,RMVar_hsa_circ_156445,RMVar_hsa_circ_324274,RMVar_hsa_circ_336800,RMVar_hsa_circ_156443,RMVar_hsa_circ_330405,RMVar_hsa_circ_283117,RMVar_hsa_circ_156450 33639 RMVar_ID_33639 Human_SNP_ID_500848562 A-to-I Human chr12 + 50431174 50431174 50431174 CCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCACTTGAACCCCGGAGGCGAAGGTT CCTGTAATCCCAGCTACTTGGGAGGCTGAGGCGGGAGAATCACTTGAACCCCGGAGGCGAAGGTT A G LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs573524009 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22547,RMVar_hsa_circ_156430,RMVar_hsa_circ_324306,RMVar_hsa_circ_368510,RMVar_hsa_circ_373064,RMVar_hsa_circ_325026,RMVar_hsa_circ_313846,RMVar_hsa_circ_156428,RMVar_hsa_circ_156429,RMVar_hsa_circ_52618,RMVar_hsa_circ_42391,RMVar_hsa_circ_270678,RMVar_hsa_circ_281157,RMVar_hsa_circ_300058,RMVar_hsa_circ_331199,RMVar_hsa_circ_362825,RMVar_hsa_circ_320194,RMVar_hsa_circ_282759,RMVar_hsa_circ_278339,RMVar_hsa_circ_275327,RMVar_hsa_circ_65767,RMVar_hsa_circ_156433,RMVar_hsa_circ_156435,RMVar_hsa_circ_156436,RMVar_hsa_circ_156434,RMVar_hsa_circ_312274,RMVar_hsa_circ_156431,RMVar_hsa_circ_156432,RMVar_hsa_circ_327428,RMVar_hsa_circ_350740,RMVar_hsa_circ_296643,RMVar_hsa_circ_284685,RMVar_hsa_circ_156441,RMVar_hsa_circ_156442,RMVar_hsa_circ_65030,RMVar_hsa_circ_42887,RMVar_hsa_circ_290610,RMVar_hsa_circ_305837,RMVar_hsa_circ_350297,RMVar_hsa_circ_310910,RMVar_hsa_circ_364298,RMVar_hsa_circ_340771,RMVar_hsa_circ_294181,RMVar_hsa_circ_273923,RMVar_hsa_circ_288347,RMVar_hsa_circ_271324,RMVar_hsa_circ_156446,RMVar_hsa_circ_156448,RMVar_hsa_circ_156449,RMVar_hsa_circ_156447,RMVar_hsa_circ_156444,RMVar_hsa_circ_156445,RMVar_hsa_circ_324274,RMVar_hsa_circ_336800,RMVar_hsa_circ_156443,RMVar_hsa_circ_330405,RMVar_hsa_circ_283117,RMVar_hsa_circ_156450 33640 RMVar_ID_33640 Human_SNP_ID_500848695 A-to-I Human chr12 + 50431778 50431778 50431778 GGCAGCAGGAGAATCACTTGAACCGGGGAGGTAGAGATTGCAGTGAGCTGAGGTTATTCCTGGGC GGCAGCAGGAGAATCACTTGAACCGGGGAGGTGGAGATTGCAGTGAGCTGAGGTTATTCCTGGGC A G LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs569694667 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11963411 RMVar_hsa_circ_22547,RMVar_hsa_circ_156430,RMVar_hsa_circ_324306,RMVar_hsa_circ_368510,RMVar_hsa_circ_373064,RMVar_hsa_circ_325026,RMVar_hsa_circ_313846,RMVar_hsa_circ_156428,RMVar_hsa_circ_156429,RMVar_hsa_circ_52618,RMVar_hsa_circ_42391,RMVar_hsa_circ_270678,RMVar_hsa_circ_281157,RMVar_hsa_circ_300058,RMVar_hsa_circ_331199,RMVar_hsa_circ_362825,RMVar_hsa_circ_320194,RMVar_hsa_circ_282759,RMVar_hsa_circ_278339,RMVar_hsa_circ_275327,RMVar_hsa_circ_65767,RMVar_hsa_circ_156433,RMVar_hsa_circ_156435,RMVar_hsa_circ_156436,RMVar_hsa_circ_156434,RMVar_hsa_circ_312274,RMVar_hsa_circ_156431,RMVar_hsa_circ_156432,RMVar_hsa_circ_327428,RMVar_hsa_circ_350740,RMVar_hsa_circ_296643,RMVar_hsa_circ_284685,RMVar_hsa_circ_156441,RMVar_hsa_circ_156442,RMVar_hsa_circ_65030,RMVar_hsa_circ_42887,RMVar_hsa_circ_290610,RMVar_hsa_circ_305837,RMVar_hsa_circ_350297,RMVar_hsa_circ_310910,RMVar_hsa_circ_364298,RMVar_hsa_circ_340771,RMVar_hsa_circ_294181,RMVar_hsa_circ_273923,RMVar_hsa_circ_288347,RMVar_hsa_circ_271324,RMVar_hsa_circ_156446,RMVar_hsa_circ_156448,RMVar_hsa_circ_156449,RMVar_hsa_circ_156447,RMVar_hsa_circ_156444,RMVar_hsa_circ_156445,RMVar_hsa_circ_324274,RMVar_hsa_circ_336800,RMVar_hsa_circ_156443,RMVar_hsa_circ_330405,RMVar_hsa_circ_283117,RMVar_hsa_circ_156450 33641 RMVar_ID_33641 Human_SNP_ID_500848727 A-to-I Human chr12 + 50431910 50431910 50431910 TTACTTTAGCCTGTACTTTGGGAGGCCAAAGTAGGTGGATCACCTGAGGTCAGGAGTTCAAGACC TTACTTTAGCCTGTACTTTGGGAGGCCAAAGTGGGTGGATCACCTGAGGTCAGGAGTTCAAGACC A G LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1217104826 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22547,RMVar_hsa_circ_156430,RMVar_hsa_circ_324306,RMVar_hsa_circ_368510,RMVar_hsa_circ_373064,RMVar_hsa_circ_325026,RMVar_hsa_circ_313846,RMVar_hsa_circ_156428,RMVar_hsa_circ_156429,RMVar_hsa_circ_52618,RMVar_hsa_circ_42391,RMVar_hsa_circ_270678,RMVar_hsa_circ_281157,RMVar_hsa_circ_300058,RMVar_hsa_circ_331199,RMVar_hsa_circ_362825,RMVar_hsa_circ_320194,RMVar_hsa_circ_282759,RMVar_hsa_circ_278339,RMVar_hsa_circ_275327,RMVar_hsa_circ_65767,RMVar_hsa_circ_156433,RMVar_hsa_circ_156435,RMVar_hsa_circ_156436,RMVar_hsa_circ_156434,RMVar_hsa_circ_312274,RMVar_hsa_circ_156431,RMVar_hsa_circ_156432,RMVar_hsa_circ_327428,RMVar_hsa_circ_350740,RMVar_hsa_circ_296643,RMVar_hsa_circ_284685,RMVar_hsa_circ_156441,RMVar_hsa_circ_156442,RMVar_hsa_circ_65030,RMVar_hsa_circ_42887,RMVar_hsa_circ_290610,RMVar_hsa_circ_305837,RMVar_hsa_circ_350297,RMVar_hsa_circ_310910,RMVar_hsa_circ_364298,RMVar_hsa_circ_340771,RMVar_hsa_circ_294181,RMVar_hsa_circ_273923,RMVar_hsa_circ_288347,RMVar_hsa_circ_271324,RMVar_hsa_circ_156446,RMVar_hsa_circ_156448,RMVar_hsa_circ_156449,RMVar_hsa_circ_156447,RMVar_hsa_circ_156444,RMVar_hsa_circ_156445,RMVar_hsa_circ_324274,RMVar_hsa_circ_336800,RMVar_hsa_circ_156443,RMVar_hsa_circ_330405,RMVar_hsa_circ_283117,RMVar_hsa_circ_156450 33642 RMVar_ID_33642 Human_SNP_ID_500848769 A-to-I Human chr12 + 50432080 50432080 50432080 ATTGCTTGAACCCAGGATGTGGAGTATGCAGTAAGCCGAGGTTGCAGCACTGCACTCCAGCCTGG ATTGCTTGAACCCAGGATGTGGAGTATGCAGTGAGCCGAGGTTGCAGCACTGCACTCCAGCCTGG A G LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1393747195 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6192944,Human_RBP_ID_11963415 RMVar_hsa_circ_22547,RMVar_hsa_circ_156430,RMVar_hsa_circ_324306,RMVar_hsa_circ_368510,RMVar_hsa_circ_373064,RMVar_hsa_circ_325026,RMVar_hsa_circ_313846,RMVar_hsa_circ_156428,RMVar_hsa_circ_156429,RMVar_hsa_circ_52618,RMVar_hsa_circ_42391,RMVar_hsa_circ_270678,RMVar_hsa_circ_281157,RMVar_hsa_circ_300058,RMVar_hsa_circ_331199,RMVar_hsa_circ_362825,RMVar_hsa_circ_320194,RMVar_hsa_circ_282759,RMVar_hsa_circ_278339,RMVar_hsa_circ_275327,RMVar_hsa_circ_65767,RMVar_hsa_circ_156433,RMVar_hsa_circ_156435,RMVar_hsa_circ_156436,RMVar_hsa_circ_156434,RMVar_hsa_circ_312274,RMVar_hsa_circ_156431,RMVar_hsa_circ_156432,RMVar_hsa_circ_327428,RMVar_hsa_circ_350740,RMVar_hsa_circ_296643,RMVar_hsa_circ_284685,RMVar_hsa_circ_156441,RMVar_hsa_circ_156442,RMVar_hsa_circ_65030,RMVar_hsa_circ_42887,RMVar_hsa_circ_290610,RMVar_hsa_circ_305837,RMVar_hsa_circ_350297,RMVar_hsa_circ_310910,RMVar_hsa_circ_364298,RMVar_hsa_circ_340771,RMVar_hsa_circ_294181,RMVar_hsa_circ_273923,RMVar_hsa_circ_288347,RMVar_hsa_circ_271324,RMVar_hsa_circ_156446,RMVar_hsa_circ_156448,RMVar_hsa_circ_156449,RMVar_hsa_circ_156447,RMVar_hsa_circ_156444,RMVar_hsa_circ_156445,RMVar_hsa_circ_324274,RMVar_hsa_circ_336800,RMVar_hsa_circ_156443,RMVar_hsa_circ_330405,RMVar_hsa_circ_283117,RMVar_hsa_circ_156450 33643 RMVar_ID_33643 Human_SNP_ID_500848883 A-to-I Human chr12 + 50432613 50432613 50432613 CTGGCGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGCGGATCACCTGA CTGGCGCAGTGGCTCACACCTGTAATCCCAGCCCTTTGGGAGGCCAAGGCAGGCGGATCACCTGA A C LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs946513830 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22547,RMVar_hsa_circ_156430,RMVar_hsa_circ_324306,RMVar_hsa_circ_368510,RMVar_hsa_circ_373064,RMVar_hsa_circ_325026,RMVar_hsa_circ_313846,RMVar_hsa_circ_156428,RMVar_hsa_circ_156429,RMVar_hsa_circ_52618,RMVar_hsa_circ_42391,RMVar_hsa_circ_270678,RMVar_hsa_circ_281157,RMVar_hsa_circ_300058,RMVar_hsa_circ_331199,RMVar_hsa_circ_362825,RMVar_hsa_circ_320194,RMVar_hsa_circ_282759,RMVar_hsa_circ_278339,RMVar_hsa_circ_275327,RMVar_hsa_circ_65767,RMVar_hsa_circ_156433,RMVar_hsa_circ_156435,RMVar_hsa_circ_156436,RMVar_hsa_circ_156434,RMVar_hsa_circ_312274,RMVar_hsa_circ_156431,RMVar_hsa_circ_156432,RMVar_hsa_circ_327428,RMVar_hsa_circ_350740,RMVar_hsa_circ_296643,RMVar_hsa_circ_284685,RMVar_hsa_circ_156441,RMVar_hsa_circ_156442,RMVar_hsa_circ_65030,RMVar_hsa_circ_42887,RMVar_hsa_circ_290610,RMVar_hsa_circ_305837,RMVar_hsa_circ_350297,RMVar_hsa_circ_310910,RMVar_hsa_circ_364298,RMVar_hsa_circ_340771,RMVar_hsa_circ_294181,RMVar_hsa_circ_273923,RMVar_hsa_circ_288347,RMVar_hsa_circ_271324,RMVar_hsa_circ_156446,RMVar_hsa_circ_156448,RMVar_hsa_circ_156449,RMVar_hsa_circ_156447,RMVar_hsa_circ_156444,RMVar_hsa_circ_156445,RMVar_hsa_circ_324274,RMVar_hsa_circ_336800,RMVar_hsa_circ_156443,RMVar_hsa_circ_330405,RMVar_hsa_circ_283117,RMVar_hsa_circ_156450 33644 RMVar_ID_33644 Human_SNP_ID_500848907 A-to-I Human chr12 + 50432689 50432689 50432689 CAGTATTAGCCTGACCAACATGGTGAAACCCCATCTCTACTTAAATACAAAAAATTAGCTGGGCA CAGTATTAGCCTGACCAACATGGTGAAACCCCGTCTCTACTTAAATACAAAAAATTAGCTGGGCA A G LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1335561410 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22547,RMVar_hsa_circ_156430,RMVar_hsa_circ_324306,RMVar_hsa_circ_368510,RMVar_hsa_circ_373064,RMVar_hsa_circ_325026,RMVar_hsa_circ_313846,RMVar_hsa_circ_156428,RMVar_hsa_circ_156429,RMVar_hsa_circ_52618,RMVar_hsa_circ_42391,RMVar_hsa_circ_270678,RMVar_hsa_circ_281157,RMVar_hsa_circ_300058,RMVar_hsa_circ_331199,RMVar_hsa_circ_362825,RMVar_hsa_circ_320194,RMVar_hsa_circ_282759,RMVar_hsa_circ_278339,RMVar_hsa_circ_275327,RMVar_hsa_circ_65767,RMVar_hsa_circ_156433,RMVar_hsa_circ_156435,RMVar_hsa_circ_156436,RMVar_hsa_circ_156434,RMVar_hsa_circ_312274,RMVar_hsa_circ_156431,RMVar_hsa_circ_156432,RMVar_hsa_circ_327428,RMVar_hsa_circ_350740,RMVar_hsa_circ_296643,RMVar_hsa_circ_284685,RMVar_hsa_circ_156441,RMVar_hsa_circ_156442,RMVar_hsa_circ_65030,RMVar_hsa_circ_42887,RMVar_hsa_circ_290610,RMVar_hsa_circ_305837,RMVar_hsa_circ_350297,RMVar_hsa_circ_310910,RMVar_hsa_circ_364298,RMVar_hsa_circ_340771,RMVar_hsa_circ_294181,RMVar_hsa_circ_273923,RMVar_hsa_circ_288347,RMVar_hsa_circ_271324,RMVar_hsa_circ_156446,RMVar_hsa_circ_156448,RMVar_hsa_circ_156449,RMVar_hsa_circ_156447,RMVar_hsa_circ_156444,RMVar_hsa_circ_156445,RMVar_hsa_circ_324274,RMVar_hsa_circ_336800,RMVar_hsa_circ_156443,RMVar_hsa_circ_330405,RMVar_hsa_circ_283117,RMVar_hsa_circ_156450 33645 RMVar_ID_33645 Human_SNP_ID_500849227 A-to-I Human chr12 + 50433785 50433785 50433785 ATTCAGCCTCCCAAGTAGCTGGGAGTACGGGCACGCACAACCGTGCCTGGCTAAGTTTTGTGTTT ATTCAGCCTCCCAAGTAGCTGGGAGTACGGGCGCGCACAACCGTGCCTGGCTAAGTTTTGTGTTT A G LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1468669881 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22547,RMVar_hsa_circ_156430,RMVar_hsa_circ_324306,RMVar_hsa_circ_368510,RMVar_hsa_circ_373064,RMVar_hsa_circ_325026,RMVar_hsa_circ_313846,RMVar_hsa_circ_156428,RMVar_hsa_circ_156429,RMVar_hsa_circ_52618,RMVar_hsa_circ_42391,RMVar_hsa_circ_270678,RMVar_hsa_circ_281157,RMVar_hsa_circ_300058,RMVar_hsa_circ_331199,RMVar_hsa_circ_362825,RMVar_hsa_circ_320194,RMVar_hsa_circ_282759,RMVar_hsa_circ_278339,RMVar_hsa_circ_275327,RMVar_hsa_circ_65767,RMVar_hsa_circ_156433,RMVar_hsa_circ_156435,RMVar_hsa_circ_156436,RMVar_hsa_circ_156434,RMVar_hsa_circ_312274,RMVar_hsa_circ_156431,RMVar_hsa_circ_156432,RMVar_hsa_circ_327428,RMVar_hsa_circ_350740,RMVar_hsa_circ_296643,RMVar_hsa_circ_284685,RMVar_hsa_circ_156441,RMVar_hsa_circ_156442,RMVar_hsa_circ_65030,RMVar_hsa_circ_42887,RMVar_hsa_circ_290610,RMVar_hsa_circ_305837,RMVar_hsa_circ_350297,RMVar_hsa_circ_310910,RMVar_hsa_circ_364298,RMVar_hsa_circ_340771,RMVar_hsa_circ_294181,RMVar_hsa_circ_273923,RMVar_hsa_circ_288347,RMVar_hsa_circ_271324,RMVar_hsa_circ_156446,RMVar_hsa_circ_156448,RMVar_hsa_circ_156449,RMVar_hsa_circ_156447,RMVar_hsa_circ_156444,RMVar_hsa_circ_156445,RMVar_hsa_circ_324274,RMVar_hsa_circ_336800,RMVar_hsa_circ_156443,RMVar_hsa_circ_330405,RMVar_hsa_circ_283117,RMVar_hsa_circ_156450 33646 RMVar_ID_33646 Human_SNP_ID_500849237 A-to-I Human chr12 + 50433805 50433804 50433806 GGGAGTACGGGCACGCACAACCGTGCCTGGCTAAGTTTTGTGTTTTTAGTAGAGACGAGGTTTTA GGGAGTACGGGCACGCACAACCGTGCCTGGCT__GTTTTGTGTTTTTAGTAGAGACGAGGTTTTA TAA T LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs944451294 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_22547,RMVar_hsa_circ_156430,RMVar_hsa_circ_324306,RMVar_hsa_circ_368510,RMVar_hsa_circ_373064,RMVar_hsa_circ_325026,RMVar_hsa_circ_313846,RMVar_hsa_circ_156428,RMVar_hsa_circ_156429,RMVar_hsa_circ_52618,RMVar_hsa_circ_42391,RMVar_hsa_circ_270678,RMVar_hsa_circ_281157,RMVar_hsa_circ_300058,RMVar_hsa_circ_331199,RMVar_hsa_circ_362825,RMVar_hsa_circ_320194,RMVar_hsa_circ_282759,RMVar_hsa_circ_278339,RMVar_hsa_circ_275327,RMVar_hsa_circ_65767,RMVar_hsa_circ_156433,RMVar_hsa_circ_156435,RMVar_hsa_circ_156436,RMVar_hsa_circ_156434,RMVar_hsa_circ_312274,RMVar_hsa_circ_156431,RMVar_hsa_circ_156432,RMVar_hsa_circ_327428,RMVar_hsa_circ_350740,RMVar_hsa_circ_296643,RMVar_hsa_circ_284685,RMVar_hsa_circ_156441,RMVar_hsa_circ_156442,RMVar_hsa_circ_65030,RMVar_hsa_circ_42887,RMVar_hsa_circ_290610,RMVar_hsa_circ_305837,RMVar_hsa_circ_350297,RMVar_hsa_circ_310910,RMVar_hsa_circ_364298,RMVar_hsa_circ_340771,RMVar_hsa_circ_294181,RMVar_hsa_circ_273923,RMVar_hsa_circ_288347,RMVar_hsa_circ_271324,RMVar_hsa_circ_156446,RMVar_hsa_circ_156448,RMVar_hsa_circ_156449,RMVar_hsa_circ_156447,RMVar_hsa_circ_156444,RMVar_hsa_circ_156445,RMVar_hsa_circ_324274,RMVar_hsa_circ_336800,RMVar_hsa_circ_156443,RMVar_hsa_circ_330405,RMVar_hsa_circ_283117,RMVar_hsa_circ_156450 33647 RMVar_ID_33647 Human_SNP_ID_500849255 A-to-I Human chr12 + 50433869 50433869 50433869 ATCATGTTGGCTAGGCTAATCTCAAACTCCTGATATCAGGTGATCCACCCACCTTTGCCTCCCAA ATCATGTTGGCTAGGCTAATCTCAAACTCCTGCTATCAGGTGATCCACCCACCTTTGCCTCCCAA A C LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10876034 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22547,RMVar_hsa_circ_156430,RMVar_hsa_circ_324306,RMVar_hsa_circ_368510,RMVar_hsa_circ_373064,RMVar_hsa_circ_325026,RMVar_hsa_circ_313846,RMVar_hsa_circ_156428,RMVar_hsa_circ_156429,RMVar_hsa_circ_52618,RMVar_hsa_circ_42391,RMVar_hsa_circ_270678,RMVar_hsa_circ_281157,RMVar_hsa_circ_300058,RMVar_hsa_circ_331199,RMVar_hsa_circ_362825,RMVar_hsa_circ_320194,RMVar_hsa_circ_282759,RMVar_hsa_circ_278339,RMVar_hsa_circ_275327,RMVar_hsa_circ_65767,RMVar_hsa_circ_156433,RMVar_hsa_circ_156435,RMVar_hsa_circ_156436,RMVar_hsa_circ_156434,RMVar_hsa_circ_312274,RMVar_hsa_circ_156431,RMVar_hsa_circ_156432,RMVar_hsa_circ_327428,RMVar_hsa_circ_350740,RMVar_hsa_circ_296643,RMVar_hsa_circ_284685,RMVar_hsa_circ_156441,RMVar_hsa_circ_156442,RMVar_hsa_circ_65030,RMVar_hsa_circ_42887,RMVar_hsa_circ_290610,RMVar_hsa_circ_305837,RMVar_hsa_circ_350297,RMVar_hsa_circ_310910,RMVar_hsa_circ_364298,RMVar_hsa_circ_340771,RMVar_hsa_circ_294181,RMVar_hsa_circ_273923,RMVar_hsa_circ_288347,RMVar_hsa_circ_271324,RMVar_hsa_circ_156446,RMVar_hsa_circ_156448,RMVar_hsa_circ_156449,RMVar_hsa_circ_156447,RMVar_hsa_circ_156444,RMVar_hsa_circ_156445,RMVar_hsa_circ_324274,RMVar_hsa_circ_336800,RMVar_hsa_circ_156443,RMVar_hsa_circ_330405,RMVar_hsa_circ_283117,RMVar_hsa_circ_156450 33648 RMVar_ID_33648 Human_SNP_ID_500849256 A-to-I Human chr12 + 50433869 50433869 50433869 ATCATGTTGGCTAGGCTAATCTCAAACTCCTGATATCAGGTGATCCACCCACCTTTGCCTCCCAA ATCATGTTGGCTAGGCTAATCTCAAACTCCTGGTATCAGGTGATCCACCCACCTTTGCCTCCCAA A G LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10876034 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22547,RMVar_hsa_circ_156430,RMVar_hsa_circ_324306,RMVar_hsa_circ_368510,RMVar_hsa_circ_373064,RMVar_hsa_circ_325026,RMVar_hsa_circ_313846,RMVar_hsa_circ_156428,RMVar_hsa_circ_156429,RMVar_hsa_circ_52618,RMVar_hsa_circ_42391,RMVar_hsa_circ_270678,RMVar_hsa_circ_281157,RMVar_hsa_circ_300058,RMVar_hsa_circ_331199,RMVar_hsa_circ_362825,RMVar_hsa_circ_320194,RMVar_hsa_circ_282759,RMVar_hsa_circ_278339,RMVar_hsa_circ_275327,RMVar_hsa_circ_65767,RMVar_hsa_circ_156433,RMVar_hsa_circ_156435,RMVar_hsa_circ_156436,RMVar_hsa_circ_156434,RMVar_hsa_circ_312274,RMVar_hsa_circ_156431,RMVar_hsa_circ_156432,RMVar_hsa_circ_327428,RMVar_hsa_circ_350740,RMVar_hsa_circ_296643,RMVar_hsa_circ_284685,RMVar_hsa_circ_156441,RMVar_hsa_circ_156442,RMVar_hsa_circ_65030,RMVar_hsa_circ_42887,RMVar_hsa_circ_290610,RMVar_hsa_circ_305837,RMVar_hsa_circ_350297,RMVar_hsa_circ_310910,RMVar_hsa_circ_364298,RMVar_hsa_circ_340771,RMVar_hsa_circ_294181,RMVar_hsa_circ_273923,RMVar_hsa_circ_288347,RMVar_hsa_circ_271324,RMVar_hsa_circ_156446,RMVar_hsa_circ_156448,RMVar_hsa_circ_156449,RMVar_hsa_circ_156447,RMVar_hsa_circ_156444,RMVar_hsa_circ_156445,RMVar_hsa_circ_324274,RMVar_hsa_circ_336800,RMVar_hsa_circ_156443,RMVar_hsa_circ_330405,RMVar_hsa_circ_283117,RMVar_hsa_circ_156450 33649 RMVar_ID_33649 Human_SNP_ID_500849423 A-to-I Human chr12 + 50434512 50434512 50434512 GTGATCTCGGCTCATTGCAATCTCCGCCTCCCAGGTTCAAGCGATTCTCTTGCCTCAGCACCCCG GTGATCTCGGCTCATTGCAATCTCCGCCTCCCGGGTTCAAGCGATTCTCTTGCCTCAGCACCCCG A G LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs976139393 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22547,RMVar_hsa_circ_156430,RMVar_hsa_circ_324306,RMVar_hsa_circ_368510,RMVar_hsa_circ_373064,RMVar_hsa_circ_325026,RMVar_hsa_circ_313846,RMVar_hsa_circ_156428,RMVar_hsa_circ_156429,RMVar_hsa_circ_52618,RMVar_hsa_circ_42391,RMVar_hsa_circ_270678,RMVar_hsa_circ_281157,RMVar_hsa_circ_300058,RMVar_hsa_circ_331199,RMVar_hsa_circ_362825,RMVar_hsa_circ_320194,RMVar_hsa_circ_282759,RMVar_hsa_circ_278339,RMVar_hsa_circ_275327,RMVar_hsa_circ_65767,RMVar_hsa_circ_156433,RMVar_hsa_circ_156435,RMVar_hsa_circ_156436,RMVar_hsa_circ_156434,RMVar_hsa_circ_312274,RMVar_hsa_circ_156431,RMVar_hsa_circ_156432,RMVar_hsa_circ_327428,RMVar_hsa_circ_350740,RMVar_hsa_circ_296643,RMVar_hsa_circ_284685,RMVar_hsa_circ_156441,RMVar_hsa_circ_156442,RMVar_hsa_circ_65030,RMVar_hsa_circ_42887,RMVar_hsa_circ_290610,RMVar_hsa_circ_305837,RMVar_hsa_circ_350297,RMVar_hsa_circ_310910,RMVar_hsa_circ_364298,RMVar_hsa_circ_340771,RMVar_hsa_circ_294181,RMVar_hsa_circ_273923,RMVar_hsa_circ_288347,RMVar_hsa_circ_271324,RMVar_hsa_circ_156446,RMVar_hsa_circ_156448,RMVar_hsa_circ_156449,RMVar_hsa_circ_156447,RMVar_hsa_circ_156444,RMVar_hsa_circ_156445,RMVar_hsa_circ_324274,RMVar_hsa_circ_336800,RMVar_hsa_circ_156443,RMVar_hsa_circ_330405,RMVar_hsa_circ_283117,RMVar_hsa_circ_156450 33650 RMVar_ID_33650 Human_SNP_ID_500852110 A-to-I Human chr12 + 50445151 50445151 50445151 TCTCTTAACTCCTGAGGGCAAGCGATCCCCCCACTAAGGCCTCCCAAAGTGTTGGGACTATAGAC TCTCTTAACTCCTGAGGGCAAGCGATCCCCCCCCTAAGGCCTCCCAAAGTGTTGGGACTATAGAC A C LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909294339 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_156430,RMVar_hsa_circ_373064,RMVar_hsa_circ_313846,RMVar_hsa_circ_156429,RMVar_hsa_circ_52618,RMVar_hsa_circ_270678,RMVar_hsa_circ_300058,RMVar_hsa_circ_362825,RMVar_hsa_circ_320194,RMVar_hsa_circ_282759,RMVar_hsa_circ_65767,RMVar_hsa_circ_156433,RMVar_hsa_circ_156431,RMVar_hsa_circ_156432,RMVar_hsa_circ_296643,RMVar_hsa_circ_284685,RMVar_hsa_circ_156442,RMVar_hsa_circ_65030,RMVar_hsa_circ_42887,RMVar_hsa_circ_305837,RMVar_hsa_circ_350297,RMVar_hsa_circ_364298,RMVar_hsa_circ_340771,RMVar_hsa_circ_271324,RMVar_hsa_circ_156444,RMVar_hsa_circ_156445,RMVar_hsa_circ_336800,RMVar_hsa_circ_156443,RMVar_hsa_circ_306867,RMVar_hsa_circ_156450,RMVar_hsa_circ_333323,RMVar_hsa_circ_317118,RMVar_hsa_circ_38780,RMVar_hsa_circ_56483,RMVar_hsa_circ_8813,RMVar_hsa_circ_156452,RMVar_hsa_circ_156453,RMVar_hsa_circ_343836,RMVar_hsa_circ_156451,RMVar_hsa_circ_343952,RMVar_hsa_circ_8042,RMVar_hsa_circ_72855,RMVar_hsa_circ_156458,RMVar_hsa_circ_156459,RMVar_hsa_circ_49027,RMVar_hsa_circ_156461,RMVar_hsa_circ_344696 33651 RMVar_ID_33651 Human_SNP_ID_500855030 A-to-I Human chr12 + 50455882 50455882 50455882 CAGCCTGGGCAATATGACGAAACATCATCTCTACCAAAAATACAAAAATTAGCTGGGCGTGGTGG CAGCCTGGGCAATATGACGAAACATCATCTCTGCCAAAAATACAAAAATTAGCTGGGCGTGGTGG A G LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs563414753 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_300058,RMVar_hsa_circ_362825,RMVar_hsa_circ_282759,RMVar_hsa_circ_65767,RMVar_hsa_circ_156431,RMVar_hsa_circ_284685,RMVar_hsa_circ_156442,RMVar_hsa_circ_65030,RMVar_hsa_circ_42887,RMVar_hsa_circ_350297,RMVar_hsa_circ_364298,RMVar_hsa_circ_340771,RMVar_hsa_circ_156443,RMVar_hsa_circ_333323,RMVar_hsa_circ_38780,RMVar_hsa_circ_56483,RMVar_hsa_circ_8813,RMVar_hsa_circ_343836,RMVar_hsa_circ_156451,RMVar_hsa_circ_8042,RMVar_hsa_circ_156459,RMVar_hsa_circ_156461,RMVar_hsa_circ_344696,RMVar_hsa_circ_320479,RMVar_hsa_circ_365181,RMVar_hsa_circ_315231,RMVar_hsa_circ_6366,RMVar_hsa_circ_156463,RMVar_hsa_circ_47930,RMVar_hsa_circ_310010,RMVar_hsa_circ_356162,RMVar_hsa_circ_337761,RMVar_hsa_circ_282545,RMVar_hsa_circ_156464,RMVar_hsa_circ_156465 33652 RMVar_ID_33652 Human_SNP_ID_500855040 A-to-I Human chr12 + 50455941 50455941 50455941 TGGTGGTGTAGTGCATGCCTGAAGTCCCAACTACTCAGGAGGCTGAGGAACGAGAATTGCTTGAG TGGTGGTGTAGTGCATGCCTGAAGTCCCAACTGCTCAGGAGGCTGAGGAACGAGAATTGCTTGAG A G LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs779904292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_421450,Human_RBP_ID_2341348,Human_RBP_ID_11964179 RMVar_hsa_circ_300058,RMVar_hsa_circ_362825,RMVar_hsa_circ_282759,RMVar_hsa_circ_65767,RMVar_hsa_circ_156431,RMVar_hsa_circ_284685,RMVar_hsa_circ_156442,RMVar_hsa_circ_65030,RMVar_hsa_circ_42887,RMVar_hsa_circ_350297,RMVar_hsa_circ_364298,RMVar_hsa_circ_340771,RMVar_hsa_circ_156443,RMVar_hsa_circ_333323,RMVar_hsa_circ_38780,RMVar_hsa_circ_56483,RMVar_hsa_circ_8813,RMVar_hsa_circ_343836,RMVar_hsa_circ_156451,RMVar_hsa_circ_8042,RMVar_hsa_circ_156459,RMVar_hsa_circ_156461,RMVar_hsa_circ_344696,RMVar_hsa_circ_320479,RMVar_hsa_circ_365181,RMVar_hsa_circ_315231,RMVar_hsa_circ_6366,RMVar_hsa_circ_156463,RMVar_hsa_circ_47930,RMVar_hsa_circ_310010,RMVar_hsa_circ_356162,RMVar_hsa_circ_337761,RMVar_hsa_circ_282545,RMVar_hsa_circ_156464,RMVar_hsa_circ_156465 33653 RMVar_ID_33653 Human_SNP_ID_500855042 A-to-I Human chr12 + 50455945 50455945 50455945 GGTGTAGTGCATGCCTGAAGTCCCAACTACTCAGGAGGCTGAGGAACGAGAATTGCTTGAGCCTG GGTGTAGTGCATGCCTGAAGTCCCAACTACTCGGGAGGCTGAGGAACGAGAATTGCTTGAGCCTG A G LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs938032680 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_421450,Human_RBP_ID_2341348,Human_RBP_ID_11964179 RMVar_hsa_circ_300058,RMVar_hsa_circ_362825,RMVar_hsa_circ_282759,RMVar_hsa_circ_65767,RMVar_hsa_circ_156431,RMVar_hsa_circ_284685,RMVar_hsa_circ_156442,RMVar_hsa_circ_65030,RMVar_hsa_circ_42887,RMVar_hsa_circ_350297,RMVar_hsa_circ_364298,RMVar_hsa_circ_340771,RMVar_hsa_circ_156443,RMVar_hsa_circ_333323,RMVar_hsa_circ_38780,RMVar_hsa_circ_56483,RMVar_hsa_circ_8813,RMVar_hsa_circ_343836,RMVar_hsa_circ_156451,RMVar_hsa_circ_8042,RMVar_hsa_circ_156459,RMVar_hsa_circ_156461,RMVar_hsa_circ_344696,RMVar_hsa_circ_320479,RMVar_hsa_circ_365181,RMVar_hsa_circ_315231,RMVar_hsa_circ_6366,RMVar_hsa_circ_156463,RMVar_hsa_circ_47930,RMVar_hsa_circ_310010,RMVar_hsa_circ_356162,RMVar_hsa_circ_337761,RMVar_hsa_circ_282545,RMVar_hsa_circ_156464,RMVar_hsa_circ_156465 33654 RMVar_ID_33654 Human_SNP_ID_500855044 A-to-I Human chr12 + 50455954 50455954 50455954 CATGCCTGAAGTCCCAACTACTCAGGAGGCTGAGGAACGAGAATTGCTTGAGCCTGAGAAGCACA CATGCCTGAAGTCCCAACTACTCAGGAGGCTGGGGAACGAGAATTGCTTGAGCCTGAGAAGCACA A G LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1184084297 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_421450,Human_RBP_ID_2341348,Human_RBP_ID_3407543,Human_RBP_ID_8377885,Human_RBP_ID_11964179 RMVar_hsa_circ_300058,RMVar_hsa_circ_362825,RMVar_hsa_circ_282759,RMVar_hsa_circ_65767,RMVar_hsa_circ_156431,RMVar_hsa_circ_284685,RMVar_hsa_circ_156442,RMVar_hsa_circ_65030,RMVar_hsa_circ_42887,RMVar_hsa_circ_350297,RMVar_hsa_circ_364298,RMVar_hsa_circ_340771,RMVar_hsa_circ_156443,RMVar_hsa_circ_333323,RMVar_hsa_circ_38780,RMVar_hsa_circ_56483,RMVar_hsa_circ_8813,RMVar_hsa_circ_343836,RMVar_hsa_circ_156451,RMVar_hsa_circ_8042,RMVar_hsa_circ_156459,RMVar_hsa_circ_156461,RMVar_hsa_circ_344696,RMVar_hsa_circ_320479,RMVar_hsa_circ_365181,RMVar_hsa_circ_315231,RMVar_hsa_circ_6366,RMVar_hsa_circ_156463,RMVar_hsa_circ_47930,RMVar_hsa_circ_310010,RMVar_hsa_circ_356162,RMVar_hsa_circ_337761,RMVar_hsa_circ_282545,RMVar_hsa_circ_156464,RMVar_hsa_circ_156465 33655 RMVar_ID_33655 Human_SNP_ID_500855299 A-to-I Human chr12 + 50457016 50457016 50457016 CTTACTGCAACCTCTGCTTCCCGAGTTCAAGCAATTCTCTGGCCTCAGCCTTCTGAGTAGCTGGG CTTACTGCAACCTCTGCTTCCCGAGTTCAAGCCATTCTCTGGCCTCAGCCTTCTGAGTAGCTGGG A C LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs897863716 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_300058,RMVar_hsa_circ_362825,RMVar_hsa_circ_282759,RMVar_hsa_circ_65767,RMVar_hsa_circ_156431,RMVar_hsa_circ_284685,RMVar_hsa_circ_156442,RMVar_hsa_circ_65030,RMVar_hsa_circ_42887,RMVar_hsa_circ_350297,RMVar_hsa_circ_364298,RMVar_hsa_circ_340771,RMVar_hsa_circ_156443,RMVar_hsa_circ_333323,RMVar_hsa_circ_38780,RMVar_hsa_circ_56483,RMVar_hsa_circ_8813,RMVar_hsa_circ_343836,RMVar_hsa_circ_156451,RMVar_hsa_circ_8042,RMVar_hsa_circ_156459,RMVar_hsa_circ_156461,RMVar_hsa_circ_344696,RMVar_hsa_circ_320479,RMVar_hsa_circ_365181,RMVar_hsa_circ_315231,RMVar_hsa_circ_6366,RMVar_hsa_circ_156463,RMVar_hsa_circ_47930,RMVar_hsa_circ_310010,RMVar_hsa_circ_356162,RMVar_hsa_circ_337761,RMVar_hsa_circ_282545,RMVar_hsa_circ_156464,RMVar_hsa_circ_156465 33656 RMVar_ID_33656 Human_SNP_ID_500855324 A-to-I Human chr12 + 50457124 50457124 50457124 CGGGGTTTCATCATGTTGGCCAGGATGGTCTCAATCTCTTGACCTCGTGATCCACCCAGCTTGGC CGGGGTTTCATCATGTTGGCCAGGATGGTCTCGATCTCTTGACCTCGTGATCCACCCAGCTTGGC A G LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs968134351 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24976515 RMVar_hsa_circ_300058,RMVar_hsa_circ_362825,RMVar_hsa_circ_282759,RMVar_hsa_circ_65767,RMVar_hsa_circ_156431,RMVar_hsa_circ_284685,RMVar_hsa_circ_156442,RMVar_hsa_circ_65030,RMVar_hsa_circ_42887,RMVar_hsa_circ_350297,RMVar_hsa_circ_364298,RMVar_hsa_circ_340771,RMVar_hsa_circ_156443,RMVar_hsa_circ_333323,RMVar_hsa_circ_38780,RMVar_hsa_circ_56483,RMVar_hsa_circ_8813,RMVar_hsa_circ_343836,RMVar_hsa_circ_156451,RMVar_hsa_circ_8042,RMVar_hsa_circ_156459,RMVar_hsa_circ_156461,RMVar_hsa_circ_344696,RMVar_hsa_circ_320479,RMVar_hsa_circ_365181,RMVar_hsa_circ_315231,RMVar_hsa_circ_6366,RMVar_hsa_circ_156463,RMVar_hsa_circ_47930,RMVar_hsa_circ_310010,RMVar_hsa_circ_356162,RMVar_hsa_circ_337761,RMVar_hsa_circ_282545,RMVar_hsa_circ_156464,RMVar_hsa_circ_156465 33657 RMVar_ID_33657 Human_SNP_ID_500855427 A-to-I Human chr12 + 50457372 50457372 50457372 GAGATTACAGACGCATGCCACCACGCCCAGCTAATTTTTTGTATTTTAGTAGAAACTGGGTTTCA GAGATTACAGACGCATGCCACCACGCCCAGCTGATTTTTTGTATTTTAGTAGAAACTGGGTTTCA A G LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1379315362 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11964249 RMVar_hsa_circ_300058,RMVar_hsa_circ_362825,RMVar_hsa_circ_282759,RMVar_hsa_circ_65767,RMVar_hsa_circ_156431,RMVar_hsa_circ_284685,RMVar_hsa_circ_156442,RMVar_hsa_circ_65030,RMVar_hsa_circ_42887,RMVar_hsa_circ_350297,RMVar_hsa_circ_364298,RMVar_hsa_circ_340771,RMVar_hsa_circ_156443,RMVar_hsa_circ_333323,RMVar_hsa_circ_38780,RMVar_hsa_circ_56483,RMVar_hsa_circ_8813,RMVar_hsa_circ_343836,RMVar_hsa_circ_156451,RMVar_hsa_circ_8042,RMVar_hsa_circ_156459,RMVar_hsa_circ_156461,RMVar_hsa_circ_344696,RMVar_hsa_circ_320479,RMVar_hsa_circ_365181,RMVar_hsa_circ_315231,RMVar_hsa_circ_6366,RMVar_hsa_circ_156463,RMVar_hsa_circ_47930,RMVar_hsa_circ_310010,RMVar_hsa_circ_356162,RMVar_hsa_circ_337761,RMVar_hsa_circ_282545,RMVar_hsa_circ_156464,RMVar_hsa_circ_156465 33658 RMVar_ID_33658 Human_SNP_ID_500855434 A-to-I Human chr12 + 50457407 50457407 50457407 TTTTTGTATTTTAGTAGAAACTGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCT TTTTTGTATTTTAGTAGAAACTGGGTTTCACCGTGTTGGCCAGGCTGGTCTCGAACTCCTGACCT A G LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1454581831 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_300058,RMVar_hsa_circ_362825,RMVar_hsa_circ_282759,RMVar_hsa_circ_65767,RMVar_hsa_circ_156431,RMVar_hsa_circ_284685,RMVar_hsa_circ_156442,RMVar_hsa_circ_65030,RMVar_hsa_circ_42887,RMVar_hsa_circ_350297,RMVar_hsa_circ_364298,RMVar_hsa_circ_340771,RMVar_hsa_circ_156443,RMVar_hsa_circ_333323,RMVar_hsa_circ_38780,RMVar_hsa_circ_56483,RMVar_hsa_circ_8813,RMVar_hsa_circ_343836,RMVar_hsa_circ_156451,RMVar_hsa_circ_8042,RMVar_hsa_circ_156459,RMVar_hsa_circ_156461,RMVar_hsa_circ_344696,RMVar_hsa_circ_320479,RMVar_hsa_circ_365181,RMVar_hsa_circ_315231,RMVar_hsa_circ_6366,RMVar_hsa_circ_156463,RMVar_hsa_circ_47930,RMVar_hsa_circ_310010,RMVar_hsa_circ_356162,RMVar_hsa_circ_337761,RMVar_hsa_circ_282545,RMVar_hsa_circ_156464,RMVar_hsa_circ_156465 33659 RMVar_ID_33659 Human_SNP_ID_500855478 A-to-I Human chr12 + 50457556 50457556 50457556 ACTTTTTATAGCCAGTGGGGTGGCTCATGCCTATATTCCCCACACATTGAGAAGCCAAGGCAGGC ACTTTTTATAGCCAGTGGGGTGGCTCATGCCTGTATTCCCCACACATTGAGAAGCCAAGGCAGGC A G LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs901905439 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_753975,Human_RBP_ID_12070460 RMVar_hsa_circ_300058,RMVar_hsa_circ_362825,RMVar_hsa_circ_282759,RMVar_hsa_circ_65767,RMVar_hsa_circ_156431,RMVar_hsa_circ_284685,RMVar_hsa_circ_156442,RMVar_hsa_circ_65030,RMVar_hsa_circ_42887,RMVar_hsa_circ_350297,RMVar_hsa_circ_364298,RMVar_hsa_circ_340771,RMVar_hsa_circ_156443,RMVar_hsa_circ_333323,RMVar_hsa_circ_38780,RMVar_hsa_circ_56483,RMVar_hsa_circ_8813,RMVar_hsa_circ_343836,RMVar_hsa_circ_156451,RMVar_hsa_circ_8042,RMVar_hsa_circ_156459,RMVar_hsa_circ_156461,RMVar_hsa_circ_344696,RMVar_hsa_circ_320479,RMVar_hsa_circ_365181,RMVar_hsa_circ_315231,RMVar_hsa_circ_6366,RMVar_hsa_circ_156463,RMVar_hsa_circ_47930,RMVar_hsa_circ_310010,RMVar_hsa_circ_356162,RMVar_hsa_circ_337761,RMVar_hsa_circ_282545,RMVar_hsa_circ_156464,RMVar_hsa_circ_156465 33660 RMVar_ID_33660 Human_SNP_ID_500855479 A-to-I Human chr12 + 50457558 50457558 50457558 TTTTTATAGCCAGTGGGGTGGCTCATGCCTATATTCCCCACACATTGAGAAGCCAAGGCAGGCAG TTTTTATAGCCAGTGGGGTGGCTCATGCCTATGTTCCCCACACATTGAGAAGCCAAGGCAGGCAG A G LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1229222981 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_753975,Human_RBP_ID_12070460 RMVar_hsa_circ_300058,RMVar_hsa_circ_362825,RMVar_hsa_circ_282759,RMVar_hsa_circ_65767,RMVar_hsa_circ_156431,RMVar_hsa_circ_284685,RMVar_hsa_circ_156442,RMVar_hsa_circ_65030,RMVar_hsa_circ_42887,RMVar_hsa_circ_350297,RMVar_hsa_circ_364298,RMVar_hsa_circ_340771,RMVar_hsa_circ_156443,RMVar_hsa_circ_333323,RMVar_hsa_circ_38780,RMVar_hsa_circ_56483,RMVar_hsa_circ_8813,RMVar_hsa_circ_343836,RMVar_hsa_circ_156451,RMVar_hsa_circ_8042,RMVar_hsa_circ_156459,RMVar_hsa_circ_156461,RMVar_hsa_circ_344696,RMVar_hsa_circ_320479,RMVar_hsa_circ_365181,RMVar_hsa_circ_315231,RMVar_hsa_circ_6366,RMVar_hsa_circ_156463,RMVar_hsa_circ_47930,RMVar_hsa_circ_310010,RMVar_hsa_circ_356162,RMVar_hsa_circ_337761,RMVar_hsa_circ_282545,RMVar_hsa_circ_156464,RMVar_hsa_circ_156465 33661 RMVar_ID_33661 Human_SNP_ID_500855489 A-to-I Human chr12 + 50457623 50457623 50457623 ATCACTTGATCTCATGAGTTGGAGACCAACCTAGGCAACAGAGTGAAACCTCGTCTCTACTGACA ATCACTTGATCTCATGAGTTGGAGACCAACCTGGGCAACAGAGTGAAACCTCGTCTCTACTGACA A G LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1384739359 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_300058,RMVar_hsa_circ_362825,RMVar_hsa_circ_282759,RMVar_hsa_circ_65767,RMVar_hsa_circ_156431,RMVar_hsa_circ_284685,RMVar_hsa_circ_156442,RMVar_hsa_circ_65030,RMVar_hsa_circ_42887,RMVar_hsa_circ_350297,RMVar_hsa_circ_364298,RMVar_hsa_circ_340771,RMVar_hsa_circ_156443,RMVar_hsa_circ_333323,RMVar_hsa_circ_38780,RMVar_hsa_circ_56483,RMVar_hsa_circ_8813,RMVar_hsa_circ_343836,RMVar_hsa_circ_156451,RMVar_hsa_circ_8042,RMVar_hsa_circ_156459,RMVar_hsa_circ_156461,RMVar_hsa_circ_344696,RMVar_hsa_circ_320479,RMVar_hsa_circ_365181,RMVar_hsa_circ_315231,RMVar_hsa_circ_6366,RMVar_hsa_circ_156463,RMVar_hsa_circ_47930,RMVar_hsa_circ_310010,RMVar_hsa_circ_356162,RMVar_hsa_circ_337761,RMVar_hsa_circ_282545,RMVar_hsa_circ_156464,RMVar_hsa_circ_156465 33662 RMVar_ID_33662 Human_SNP_ID_500855564 A-to-I Human chr12 + 50457952 50457952 50457952 TGAAACTCAACCCAACTTTTTTTTTTTTTTTTAAGACAGTGTTTTGCCCTGTCACCCAGGCTGTA TGAAACTCAACCCAACTTTTTTTTTTTTTTTTTAGACAGTGTTTTGCCCTGTCACCCAGGCTGTA A T LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1342312130 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2341372,Human_RBP_ID_11964254,Human_RBP_ID_17561107,Human_RBP_ID_23305917 RMVar_hsa_circ_300058,RMVar_hsa_circ_362825,RMVar_hsa_circ_282759,RMVar_hsa_circ_65767,RMVar_hsa_circ_156431,RMVar_hsa_circ_284685,RMVar_hsa_circ_156442,RMVar_hsa_circ_65030,RMVar_hsa_circ_42887,RMVar_hsa_circ_350297,RMVar_hsa_circ_364298,RMVar_hsa_circ_340771,RMVar_hsa_circ_156443,RMVar_hsa_circ_333323,RMVar_hsa_circ_38780,RMVar_hsa_circ_56483,RMVar_hsa_circ_8813,RMVar_hsa_circ_343836,RMVar_hsa_circ_156451,RMVar_hsa_circ_8042,RMVar_hsa_circ_156459,RMVar_hsa_circ_156461,RMVar_hsa_circ_344696,RMVar_hsa_circ_320479,RMVar_hsa_circ_365181,RMVar_hsa_circ_315231,RMVar_hsa_circ_6366,RMVar_hsa_circ_156463,RMVar_hsa_circ_47930,RMVar_hsa_circ_310010,RMVar_hsa_circ_356162,RMVar_hsa_circ_337761,RMVar_hsa_circ_282545,RMVar_hsa_circ_156464,RMVar_hsa_circ_156465 33663 RMVar_ID_33663 Human_SNP_ID_500855584 A-to-I Human chr12 + 50458027 50458027 50458027 ATGATCATGGCTCACTGTAGTTTTGACCTCCCAGGCCCAATCAATTCTCCACCTCAGCCTTCCTA ATGATCATGGCTCACTGTAGTTTTGACCTCCCGGGCCCAATCAATTCTCCACCTCAGCCTTCCTA A G LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs186931245 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2341375,Human_RBP_ID_8377902,Human_RBP_ID_11964256 RMVar_hsa_circ_300058,RMVar_hsa_circ_362825,RMVar_hsa_circ_282759,RMVar_hsa_circ_65767,RMVar_hsa_circ_156431,RMVar_hsa_circ_284685,RMVar_hsa_circ_156442,RMVar_hsa_circ_65030,RMVar_hsa_circ_42887,RMVar_hsa_circ_350297,RMVar_hsa_circ_364298,RMVar_hsa_circ_340771,RMVar_hsa_circ_156443,RMVar_hsa_circ_333323,RMVar_hsa_circ_38780,RMVar_hsa_circ_56483,RMVar_hsa_circ_8813,RMVar_hsa_circ_343836,RMVar_hsa_circ_156451,RMVar_hsa_circ_8042,RMVar_hsa_circ_156459,RMVar_hsa_circ_156461,RMVar_hsa_circ_344696,RMVar_hsa_circ_320479,RMVar_hsa_circ_365181,RMVar_hsa_circ_315231,RMVar_hsa_circ_6366,RMVar_hsa_circ_156463,RMVar_hsa_circ_47930,RMVar_hsa_circ_310010,RMVar_hsa_circ_356162,RMVar_hsa_circ_337761,RMVar_hsa_circ_282545,RMVar_hsa_circ_156464,RMVar_hsa_circ_156465 33664 RMVar_ID_33664 Human_SNP_ID_500855586 A-to-I Human chr12 + 50458037 50458037 50458037 CTCACTGTAGTTTTGACCTCCCAGGCCCAATCAATTCTCCACCTCAGCCTTCCTAGTAGCTGGGA CTCACTGTAGTTTTGACCTCCCAGGCCCAATCGATTCTCCACCTCAGCCTTCCTAGTAGCTGGGA A G LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs993768918 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_300058,RMVar_hsa_circ_362825,RMVar_hsa_circ_282759,RMVar_hsa_circ_65767,RMVar_hsa_circ_156431,RMVar_hsa_circ_284685,RMVar_hsa_circ_156442,RMVar_hsa_circ_65030,RMVar_hsa_circ_42887,RMVar_hsa_circ_350297,RMVar_hsa_circ_364298,RMVar_hsa_circ_340771,RMVar_hsa_circ_156443,RMVar_hsa_circ_333323,RMVar_hsa_circ_38780,RMVar_hsa_circ_56483,RMVar_hsa_circ_8813,RMVar_hsa_circ_343836,RMVar_hsa_circ_156451,RMVar_hsa_circ_8042,RMVar_hsa_circ_156459,RMVar_hsa_circ_156461,RMVar_hsa_circ_344696,RMVar_hsa_circ_320479,RMVar_hsa_circ_365181,RMVar_hsa_circ_315231,RMVar_hsa_circ_6366,RMVar_hsa_circ_156463,RMVar_hsa_circ_47930,RMVar_hsa_circ_310010,RMVar_hsa_circ_356162,RMVar_hsa_circ_337761,RMVar_hsa_circ_282545,RMVar_hsa_circ_156464,RMVar_hsa_circ_156465 33665 RMVar_ID_33665 Human_SNP_ID_500855590 A-to-I Human chr12 + 50458050 50458050 50458050 TGACCTCCCAGGCCCAATCAATTCTCCACCTCAGCCTTCCTAGTAGCTGGGACTACAGGCGCATA TGACCTCCCAGGCCCAATCAATTCTCCACCTCGGCCTTCCTAGTAGCTGGGACTACAGGCGCATA A G LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1303651083 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_300058,RMVar_hsa_circ_362825,RMVar_hsa_circ_282759,RMVar_hsa_circ_65767,RMVar_hsa_circ_156431,RMVar_hsa_circ_284685,RMVar_hsa_circ_156442,RMVar_hsa_circ_65030,RMVar_hsa_circ_42887,RMVar_hsa_circ_350297,RMVar_hsa_circ_364298,RMVar_hsa_circ_340771,RMVar_hsa_circ_156443,RMVar_hsa_circ_333323,RMVar_hsa_circ_38780,RMVar_hsa_circ_56483,RMVar_hsa_circ_8813,RMVar_hsa_circ_343836,RMVar_hsa_circ_156451,RMVar_hsa_circ_8042,RMVar_hsa_circ_156459,RMVar_hsa_circ_156461,RMVar_hsa_circ_344696,RMVar_hsa_circ_320479,RMVar_hsa_circ_365181,RMVar_hsa_circ_315231,RMVar_hsa_circ_6366,RMVar_hsa_circ_156463,RMVar_hsa_circ_47930,RMVar_hsa_circ_310010,RMVar_hsa_circ_356162,RMVar_hsa_circ_337761,RMVar_hsa_circ_282545,RMVar_hsa_circ_156464,RMVar_hsa_circ_156465 33666 RMVar_ID_33666 Human_SNP_ID_500855600 A-to-I Human chr12 + 50458094 50458094 50458094 AGCTGGGACTACAGGCGCATACCACCATGCCTAGCTAAGTTTTTGTATTTTTTTTTTTGTAAAGA AGCTGGGACTACAGGCGCATACCACCATGCCTGGCTAAGTTTTTGTATTTTTTTTTTTGTAAAGA A G LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs968503159 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11964261 RMVar_hsa_circ_300058,RMVar_hsa_circ_362825,RMVar_hsa_circ_282759,RMVar_hsa_circ_65767,RMVar_hsa_circ_156431,RMVar_hsa_circ_284685,RMVar_hsa_circ_156442,RMVar_hsa_circ_65030,RMVar_hsa_circ_42887,RMVar_hsa_circ_350297,RMVar_hsa_circ_364298,RMVar_hsa_circ_340771,RMVar_hsa_circ_156443,RMVar_hsa_circ_333323,RMVar_hsa_circ_38780,RMVar_hsa_circ_56483,RMVar_hsa_circ_8813,RMVar_hsa_circ_343836,RMVar_hsa_circ_156451,RMVar_hsa_circ_8042,RMVar_hsa_circ_156459,RMVar_hsa_circ_156461,RMVar_hsa_circ_344696,RMVar_hsa_circ_320479,RMVar_hsa_circ_365181,RMVar_hsa_circ_315231,RMVar_hsa_circ_6366,RMVar_hsa_circ_156463,RMVar_hsa_circ_47930,RMVar_hsa_circ_310010,RMVar_hsa_circ_356162,RMVar_hsa_circ_337761,RMVar_hsa_circ_282545,RMVar_hsa_circ_156464,RMVar_hsa_circ_156465 33667 RMVar_ID_33667 Human_SNP_ID_500855615 A-to-I Human chr12 + 50458139 50458139 50458139 TATTTTTTTTTTTGTAAAGACAGGGTTTTGCCATGTTGTGCAGGCTGGTCTCAAACTCCTGGGCT TATTTTTTTTTTTGTAAAGACAGGGTTTTGCCGTGTTGTGCAGGCTGGTCTCAAACTCCTGGGCT A G LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs770194623 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11964262 RMVar_hsa_circ_300058,RMVar_hsa_circ_362825,RMVar_hsa_circ_282759,RMVar_hsa_circ_65767,RMVar_hsa_circ_156431,RMVar_hsa_circ_284685,RMVar_hsa_circ_156442,RMVar_hsa_circ_65030,RMVar_hsa_circ_42887,RMVar_hsa_circ_350297,RMVar_hsa_circ_364298,RMVar_hsa_circ_340771,RMVar_hsa_circ_156443,RMVar_hsa_circ_333323,RMVar_hsa_circ_38780,RMVar_hsa_circ_56483,RMVar_hsa_circ_8813,RMVar_hsa_circ_343836,RMVar_hsa_circ_156451,RMVar_hsa_circ_8042,RMVar_hsa_circ_156459,RMVar_hsa_circ_156461,RMVar_hsa_circ_344696,RMVar_hsa_circ_320479,RMVar_hsa_circ_365181,RMVar_hsa_circ_315231,RMVar_hsa_circ_6366,RMVar_hsa_circ_156463,RMVar_hsa_circ_47930,RMVar_hsa_circ_310010,RMVar_hsa_circ_356162,RMVar_hsa_circ_337761,RMVar_hsa_circ_282545,RMVar_hsa_circ_156464,RMVar_hsa_circ_156465 33668 RMVar_ID_33668 Human_SNP_ID_500855629 A-to-I Human chr12 + 50458186 50458186 50458186 GTCTCAAACTCCTGGGCTCCAATGATCCTCCCACCTCAGCCTCTTAAAGTGCTGGGGTTACAGAT GTCTCAAACTCCTGGGCTCCAATGATCCTCCCGCCTCAGCCTCTTAAAGTGCTGGGGTTACAGAT A G LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1324117179 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_300058,RMVar_hsa_circ_362825,RMVar_hsa_circ_282759,RMVar_hsa_circ_65767,RMVar_hsa_circ_156431,RMVar_hsa_circ_284685,RMVar_hsa_circ_156442,RMVar_hsa_circ_65030,RMVar_hsa_circ_42887,RMVar_hsa_circ_350297,RMVar_hsa_circ_364298,RMVar_hsa_circ_340771,RMVar_hsa_circ_156443,RMVar_hsa_circ_333323,RMVar_hsa_circ_38780,RMVar_hsa_circ_56483,RMVar_hsa_circ_8813,RMVar_hsa_circ_343836,RMVar_hsa_circ_156451,RMVar_hsa_circ_8042,RMVar_hsa_circ_156459,RMVar_hsa_circ_156461,RMVar_hsa_circ_344696,RMVar_hsa_circ_320479,RMVar_hsa_circ_365181,RMVar_hsa_circ_315231,RMVar_hsa_circ_6366,RMVar_hsa_circ_156463,RMVar_hsa_circ_47930,RMVar_hsa_circ_310010,RMVar_hsa_circ_356162,RMVar_hsa_circ_337761,RMVar_hsa_circ_282545,RMVar_hsa_circ_156464,RMVar_hsa_circ_156465 33669 RMVar_ID_33669 Human_SNP_ID_500855671 A-to-I Human chr12 + 50458329 50458329 50458329 TTTTGTATTTTTAGTTAGAGACAGAGGGTTTCACCATGTTGGCCAGGGTGGTCTTGATCTCTTGA TTTTGTATTTTTAGTTAGAGACAGAGGGTTTCGCCATGTTGGCCAGGGTGGTCTTGATCTCTTGA A G LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs976634405 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11964275,Human_RBP_ID_18261141 RMVar_hsa_circ_300058,RMVar_hsa_circ_362825,RMVar_hsa_circ_282759,RMVar_hsa_circ_65767,RMVar_hsa_circ_156431,RMVar_hsa_circ_284685,RMVar_hsa_circ_156442,RMVar_hsa_circ_65030,RMVar_hsa_circ_42887,RMVar_hsa_circ_350297,RMVar_hsa_circ_364298,RMVar_hsa_circ_340771,RMVar_hsa_circ_156443,RMVar_hsa_circ_333323,RMVar_hsa_circ_38780,RMVar_hsa_circ_56483,RMVar_hsa_circ_8813,RMVar_hsa_circ_343836,RMVar_hsa_circ_156451,RMVar_hsa_circ_8042,RMVar_hsa_circ_156459,RMVar_hsa_circ_156461,RMVar_hsa_circ_344696,RMVar_hsa_circ_320479,RMVar_hsa_circ_365181,RMVar_hsa_circ_315231,RMVar_hsa_circ_6366,RMVar_hsa_circ_156463,RMVar_hsa_circ_47930,RMVar_hsa_circ_310010,RMVar_hsa_circ_356162,RMVar_hsa_circ_337761,RMVar_hsa_circ_282545,RMVar_hsa_circ_156464,RMVar_hsa_circ_156465 33670 RMVar_ID_33670 Human_SNP_ID_500855860 A-to-I Human chr12 + 50459128 50459128 50459128 TCAAGAGATTCTCCTGCCTCAGCCTCCTGAATAGCTGGGATTACAGGTGTTTGCCACCATGCCAG TCAAGAGATTCTCCTGCCTCAGCCTCCTGAATGGCTGGGATTACAGGTGTTTGCCACCATGCCAG A G LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1283811606 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23563080 RMVar_hsa_circ_300058,RMVar_hsa_circ_362825,RMVar_hsa_circ_282759,RMVar_hsa_circ_65767,RMVar_hsa_circ_156431,RMVar_hsa_circ_284685,RMVar_hsa_circ_156442,RMVar_hsa_circ_65030,RMVar_hsa_circ_42887,RMVar_hsa_circ_350297,RMVar_hsa_circ_364298,RMVar_hsa_circ_340771,RMVar_hsa_circ_156443,RMVar_hsa_circ_333323,RMVar_hsa_circ_38780,RMVar_hsa_circ_56483,RMVar_hsa_circ_8813,RMVar_hsa_circ_343836,RMVar_hsa_circ_156451,RMVar_hsa_circ_8042,RMVar_hsa_circ_156459,RMVar_hsa_circ_156461,RMVar_hsa_circ_344696,RMVar_hsa_circ_320479,RMVar_hsa_circ_365181,RMVar_hsa_circ_315231,RMVar_hsa_circ_6366,RMVar_hsa_circ_156463,RMVar_hsa_circ_47930,RMVar_hsa_circ_310010,RMVar_hsa_circ_356162,RMVar_hsa_circ_337761,RMVar_hsa_circ_282545,RMVar_hsa_circ_156464,RMVar_hsa_circ_156465 33671 RMVar_ID_33671 Human_SNP_ID_500855875 A-to-I Human chr12 + 50459164 50459164 50459164 GGGATTACAGGTGTTTGCCACCATGCCAGGCTAATTTTTGTATTTTTAGTAGAGATGGGGATTCA GGGATTACAGGTGTTTGCCACCATGCCAGGCTGATTTTTGTATTTTTAGTAGAGATGGGGATTCA A G LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1024353443 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_300058,RMVar_hsa_circ_362825,RMVar_hsa_circ_282759,RMVar_hsa_circ_65767,RMVar_hsa_circ_156431,RMVar_hsa_circ_284685,RMVar_hsa_circ_156442,RMVar_hsa_circ_65030,RMVar_hsa_circ_42887,RMVar_hsa_circ_350297,RMVar_hsa_circ_364298,RMVar_hsa_circ_340771,RMVar_hsa_circ_156443,RMVar_hsa_circ_333323,RMVar_hsa_circ_38780,RMVar_hsa_circ_56483,RMVar_hsa_circ_8813,RMVar_hsa_circ_343836,RMVar_hsa_circ_156451,RMVar_hsa_circ_8042,RMVar_hsa_circ_156459,RMVar_hsa_circ_156461,RMVar_hsa_circ_344696,RMVar_hsa_circ_320479,RMVar_hsa_circ_365181,RMVar_hsa_circ_315231,RMVar_hsa_circ_6366,RMVar_hsa_circ_156463,RMVar_hsa_circ_47930,RMVar_hsa_circ_310010,RMVar_hsa_circ_356162,RMVar_hsa_circ_337761,RMVar_hsa_circ_282545,RMVar_hsa_circ_156464,RMVar_hsa_circ_156465 33672 RMVar_ID_33672 Human_SNP_ID_500855876 A-to-I Human chr12 + 50459173 50459173 50459173 GGTGTTTGCCACCATGCCAGGCTAATTTTTGTATTTTTAGTAGAGATGGGGATTCACCATGTTAG GGTGTTTGCCACCATGCCAGGCTAATTTTTGTGTTTTTAGTAGAGATGGGGATTCACCATGTTAG A G LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1435367008 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_300058,RMVar_hsa_circ_362825,RMVar_hsa_circ_282759,RMVar_hsa_circ_65767,RMVar_hsa_circ_156431,RMVar_hsa_circ_284685,RMVar_hsa_circ_156442,RMVar_hsa_circ_65030,RMVar_hsa_circ_42887,RMVar_hsa_circ_350297,RMVar_hsa_circ_364298,RMVar_hsa_circ_340771,RMVar_hsa_circ_156443,RMVar_hsa_circ_333323,RMVar_hsa_circ_38780,RMVar_hsa_circ_56483,RMVar_hsa_circ_8813,RMVar_hsa_circ_343836,RMVar_hsa_circ_156451,RMVar_hsa_circ_8042,RMVar_hsa_circ_156459,RMVar_hsa_circ_156461,RMVar_hsa_circ_344696,RMVar_hsa_circ_320479,RMVar_hsa_circ_365181,RMVar_hsa_circ_315231,RMVar_hsa_circ_6366,RMVar_hsa_circ_156463,RMVar_hsa_circ_47930,RMVar_hsa_circ_310010,RMVar_hsa_circ_356162,RMVar_hsa_circ_337761,RMVar_hsa_circ_282545,RMVar_hsa_circ_156464,RMVar_hsa_circ_156465 33673 RMVar_ID_33673 Human_SNP_ID_500855878 A-to-I Human chr12 + 50459182 50459182 50459182 CACCATGCCAGGCTAATTTTTGTATTTTTAGTAGAGATGGGGATTCACCATGTTAGCCAGGCTGG CACCATGCCAGGCTAATTTTTGTATTTTTAGTGGAGATGGGGATTCACCATGTTAGCCAGGCTGG A G LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1190678912 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_300058,RMVar_hsa_circ_362825,RMVar_hsa_circ_282759,RMVar_hsa_circ_65767,RMVar_hsa_circ_156431,RMVar_hsa_circ_284685,RMVar_hsa_circ_156442,RMVar_hsa_circ_65030,RMVar_hsa_circ_42887,RMVar_hsa_circ_350297,RMVar_hsa_circ_364298,RMVar_hsa_circ_340771,RMVar_hsa_circ_156443,RMVar_hsa_circ_333323,RMVar_hsa_circ_38780,RMVar_hsa_circ_56483,RMVar_hsa_circ_8813,RMVar_hsa_circ_343836,RMVar_hsa_circ_156451,RMVar_hsa_circ_8042,RMVar_hsa_circ_156459,RMVar_hsa_circ_156461,RMVar_hsa_circ_344696,RMVar_hsa_circ_320479,RMVar_hsa_circ_365181,RMVar_hsa_circ_315231,RMVar_hsa_circ_6366,RMVar_hsa_circ_156463,RMVar_hsa_circ_47930,RMVar_hsa_circ_310010,RMVar_hsa_circ_356162,RMVar_hsa_circ_337761,RMVar_hsa_circ_282545,RMVar_hsa_circ_156464,RMVar_hsa_circ_156465 33674 RMVar_ID_33674 Human_SNP_ID_500855881 A-to-I Human chr12 + 50459204 50459204 50459204 TATTTTTAGTAGAGATGGGGATTCACCATGTTAGCCAGGCTGGTCTAGAACTCCTGACCTCAGGT TATTTTTAGTAGAGATGGGGATTCACCATGTTGGCCAGGCTGGTCTAGAACTCCTGACCTCAGGT A G LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1240237181 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_300058,RMVar_hsa_circ_362825,RMVar_hsa_circ_282759,RMVar_hsa_circ_65767,RMVar_hsa_circ_156431,RMVar_hsa_circ_284685,RMVar_hsa_circ_156442,RMVar_hsa_circ_65030,RMVar_hsa_circ_42887,RMVar_hsa_circ_350297,RMVar_hsa_circ_364298,RMVar_hsa_circ_340771,RMVar_hsa_circ_156443,RMVar_hsa_circ_333323,RMVar_hsa_circ_38780,RMVar_hsa_circ_56483,RMVar_hsa_circ_8813,RMVar_hsa_circ_343836,RMVar_hsa_circ_156451,RMVar_hsa_circ_8042,RMVar_hsa_circ_156459,RMVar_hsa_circ_156461,RMVar_hsa_circ_344696,RMVar_hsa_circ_320479,RMVar_hsa_circ_365181,RMVar_hsa_circ_315231,RMVar_hsa_circ_6366,RMVar_hsa_circ_156463,RMVar_hsa_circ_47930,RMVar_hsa_circ_310010,RMVar_hsa_circ_356162,RMVar_hsa_circ_337761,RMVar_hsa_circ_282545,RMVar_hsa_circ_156464,RMVar_hsa_circ_156465 33675 RMVar_ID_33675 Human_SNP_ID_500856003 A-to-I Human chr12 + 50459677 50459677 50459677 GAAACCCCATCTCTACTAAAAATACAAAAATTATCTAGGTGTGGTGGCACGTGCCTATAGTCCCA GAAACCCCATCTCTACTAAAAATACAAAAATTTTCTAGGTGTGGTGGCACGTGCCTATAGTCCCA A T LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893226673 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_300058,RMVar_hsa_circ_362825,RMVar_hsa_circ_282759,RMVar_hsa_circ_65767,RMVar_hsa_circ_156431,RMVar_hsa_circ_284685,RMVar_hsa_circ_156442,RMVar_hsa_circ_65030,RMVar_hsa_circ_42887,RMVar_hsa_circ_350297,RMVar_hsa_circ_364298,RMVar_hsa_circ_340771,RMVar_hsa_circ_156443,RMVar_hsa_circ_333323,RMVar_hsa_circ_38780,RMVar_hsa_circ_56483,RMVar_hsa_circ_8813,RMVar_hsa_circ_343836,RMVar_hsa_circ_156451,RMVar_hsa_circ_8042,RMVar_hsa_circ_156459,RMVar_hsa_circ_156461,RMVar_hsa_circ_344696,RMVar_hsa_circ_320479,RMVar_hsa_circ_365181,RMVar_hsa_circ_315231,RMVar_hsa_circ_6366,RMVar_hsa_circ_156463,RMVar_hsa_circ_47930,RMVar_hsa_circ_310010,RMVar_hsa_circ_356162,RMVar_hsa_circ_337761,RMVar_hsa_circ_282545,RMVar_hsa_circ_156464,RMVar_hsa_circ_156465 33676 RMVar_ID_33676 Human_SNP_ID_500856010 A-to-I Human chr12 + 50459701 50459701 50459701 CAAAAATTATCTAGGTGTGGTGGCACGTGCCTATAGTCCCAGCTACTCGGGAGGCTGAGGCAGGA CAAAAATTATCTAGGTGTGGTGGCACGTGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGA A G LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs146781494 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_300058,RMVar_hsa_circ_362825,RMVar_hsa_circ_282759,RMVar_hsa_circ_65767,RMVar_hsa_circ_156431,RMVar_hsa_circ_284685,RMVar_hsa_circ_156442,RMVar_hsa_circ_65030,RMVar_hsa_circ_42887,RMVar_hsa_circ_350297,RMVar_hsa_circ_364298,RMVar_hsa_circ_340771,RMVar_hsa_circ_156443,RMVar_hsa_circ_333323,RMVar_hsa_circ_38780,RMVar_hsa_circ_56483,RMVar_hsa_circ_8813,RMVar_hsa_circ_343836,RMVar_hsa_circ_156451,RMVar_hsa_circ_8042,RMVar_hsa_circ_156459,RMVar_hsa_circ_156461,RMVar_hsa_circ_344696,RMVar_hsa_circ_320479,RMVar_hsa_circ_365181,RMVar_hsa_circ_315231,RMVar_hsa_circ_6366,RMVar_hsa_circ_156463,RMVar_hsa_circ_47930,RMVar_hsa_circ_310010,RMVar_hsa_circ_356162,RMVar_hsa_circ_337761,RMVar_hsa_circ_282545,RMVar_hsa_circ_156464,RMVar_hsa_circ_156465 33677 RMVar_ID_33677 Human_SNP_ID_500856011 A-to-I Human chr12 + 50459703 50459703 50459703 AAAATTATCTAGGTGTGGTGGCACGTGCCTATAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTATCTAGGTGTGGTGGCACGTGCCTATTGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA A T LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1427161982 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_300058,RMVar_hsa_circ_362825,RMVar_hsa_circ_282759,RMVar_hsa_circ_65767,RMVar_hsa_circ_156431,RMVar_hsa_circ_284685,RMVar_hsa_circ_156442,RMVar_hsa_circ_65030,RMVar_hsa_circ_42887,RMVar_hsa_circ_350297,RMVar_hsa_circ_364298,RMVar_hsa_circ_340771,RMVar_hsa_circ_156443,RMVar_hsa_circ_333323,RMVar_hsa_circ_38780,RMVar_hsa_circ_56483,RMVar_hsa_circ_8813,RMVar_hsa_circ_343836,RMVar_hsa_circ_156451,RMVar_hsa_circ_8042,RMVar_hsa_circ_156459,RMVar_hsa_circ_156461,RMVar_hsa_circ_344696,RMVar_hsa_circ_320479,RMVar_hsa_circ_365181,RMVar_hsa_circ_315231,RMVar_hsa_circ_6366,RMVar_hsa_circ_156463,RMVar_hsa_circ_47930,RMVar_hsa_circ_310010,RMVar_hsa_circ_356162,RMVar_hsa_circ_337761,RMVar_hsa_circ_282545,RMVar_hsa_circ_156464,RMVar_hsa_circ_156465 33678 RMVar_ID_33678 Human_SNP_ID_500856259 A-to-I Human chr12 + 50460452 50460452 50460452 TGGGCCCAAGCAGTCTTCTGCCTCAGCCTTCCAAGTAGCTGGGCATATTATAGGTGCATACCACT TGGGCCCAAGCAGTCTTCTGCCTCAGCCTTCCGAGTAGCTGGGCATATTATAGGTGCATACCACT A G LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1004756648 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_300058,RMVar_hsa_circ_362825,RMVar_hsa_circ_282759,RMVar_hsa_circ_65767,RMVar_hsa_circ_156431,RMVar_hsa_circ_284685,RMVar_hsa_circ_156442,RMVar_hsa_circ_65030,RMVar_hsa_circ_42887,RMVar_hsa_circ_350297,RMVar_hsa_circ_364298,RMVar_hsa_circ_340771,RMVar_hsa_circ_156443,RMVar_hsa_circ_333323,RMVar_hsa_circ_38780,RMVar_hsa_circ_56483,RMVar_hsa_circ_8813,RMVar_hsa_circ_343836,RMVar_hsa_circ_156451,RMVar_hsa_circ_8042,RMVar_hsa_circ_156459,RMVar_hsa_circ_156461,RMVar_hsa_circ_344696,RMVar_hsa_circ_320479,RMVar_hsa_circ_365181,RMVar_hsa_circ_315231,RMVar_hsa_circ_6366,RMVar_hsa_circ_156463,RMVar_hsa_circ_47930,RMVar_hsa_circ_310010,RMVar_hsa_circ_356162,RMVar_hsa_circ_337761,RMVar_hsa_circ_282545,RMVar_hsa_circ_156464,RMVar_hsa_circ_156465 33679 RMVar_ID_33679 Human_SNP_ID_500856261 A-to-I Human chr12 + 50460456 50460456 50460456 CCCAAGCAGTCTTCTGCCTCAGCCTTCCAAGTAGCTGGGCATATTATAGGTGCATACCACTGCAC CCCAAGCAGTCTTCTGCCTCAGCCTTCCAAGTGGCTGGGCATATTATAGGTGCATACCACTGCAC A G LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1471375915 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_300058,RMVar_hsa_circ_362825,RMVar_hsa_circ_282759,RMVar_hsa_circ_65767,RMVar_hsa_circ_156431,RMVar_hsa_circ_284685,RMVar_hsa_circ_156442,RMVar_hsa_circ_65030,RMVar_hsa_circ_42887,RMVar_hsa_circ_350297,RMVar_hsa_circ_364298,RMVar_hsa_circ_340771,RMVar_hsa_circ_156443,RMVar_hsa_circ_333323,RMVar_hsa_circ_38780,RMVar_hsa_circ_56483,RMVar_hsa_circ_8813,RMVar_hsa_circ_343836,RMVar_hsa_circ_156451,RMVar_hsa_circ_8042,RMVar_hsa_circ_156459,RMVar_hsa_circ_156461,RMVar_hsa_circ_344696,RMVar_hsa_circ_320479,RMVar_hsa_circ_365181,RMVar_hsa_circ_315231,RMVar_hsa_circ_6366,RMVar_hsa_circ_156463,RMVar_hsa_circ_47930,RMVar_hsa_circ_310010,RMVar_hsa_circ_356162,RMVar_hsa_circ_337761,RMVar_hsa_circ_282545,RMVar_hsa_circ_156464,RMVar_hsa_circ_156465 33680 RMVar_ID_33680 Human_SNP_ID_500856286 A-to-I Human chr12 + 50460585 50460585 50460585 ATCTCAAACAATCCTCCTGCCTCAGCCTCCCAAAGTGCTGAGATTACAGGCGTGAGCCACTGTGT ATCTCAAACAATCCTCCTGCCTCAGCCTCCCATAGTGCTGAGATTACAGGCGTGAGCCACTGTGT A T LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1380033848 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_300058,RMVar_hsa_circ_362825,RMVar_hsa_circ_282759,RMVar_hsa_circ_65767,RMVar_hsa_circ_156431,RMVar_hsa_circ_284685,RMVar_hsa_circ_156442,RMVar_hsa_circ_65030,RMVar_hsa_circ_42887,RMVar_hsa_circ_350297,RMVar_hsa_circ_364298,RMVar_hsa_circ_340771,RMVar_hsa_circ_156443,RMVar_hsa_circ_333323,RMVar_hsa_circ_38780,RMVar_hsa_circ_56483,RMVar_hsa_circ_8813,RMVar_hsa_circ_343836,RMVar_hsa_circ_156451,RMVar_hsa_circ_8042,RMVar_hsa_circ_156459,RMVar_hsa_circ_156461,RMVar_hsa_circ_344696,RMVar_hsa_circ_320479,RMVar_hsa_circ_365181,RMVar_hsa_circ_315231,RMVar_hsa_circ_6366,RMVar_hsa_circ_156463,RMVar_hsa_circ_47930,RMVar_hsa_circ_310010,RMVar_hsa_circ_356162,RMVar_hsa_circ_337761,RMVar_hsa_circ_282545,RMVar_hsa_circ_156464,RMVar_hsa_circ_156465 33681 RMVar_ID_33681 Human_SNP_ID_500856347 A-to-I Human chr12 + 50460822 50460822 50460822 AAAATTAGCTGGACGTGGTGGCTGGCGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA AAAATTAGCTGGACGTGGTGGCTGGCGCCTGTGGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA A G LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1232592704 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_300058,RMVar_hsa_circ_362825,RMVar_hsa_circ_282759,RMVar_hsa_circ_65767,RMVar_hsa_circ_156431,RMVar_hsa_circ_284685,RMVar_hsa_circ_156442,RMVar_hsa_circ_65030,RMVar_hsa_circ_42887,RMVar_hsa_circ_350297,RMVar_hsa_circ_364298,RMVar_hsa_circ_340771,RMVar_hsa_circ_156443,RMVar_hsa_circ_333323,RMVar_hsa_circ_38780,RMVar_hsa_circ_56483,RMVar_hsa_circ_8813,RMVar_hsa_circ_343836,RMVar_hsa_circ_156451,RMVar_hsa_circ_8042,RMVar_hsa_circ_156459,RMVar_hsa_circ_156461,RMVar_hsa_circ_344696,RMVar_hsa_circ_320479,RMVar_hsa_circ_365181,RMVar_hsa_circ_315231,RMVar_hsa_circ_6366,RMVar_hsa_circ_156463,RMVar_hsa_circ_47930,RMVar_hsa_circ_310010,RMVar_hsa_circ_356162,RMVar_hsa_circ_337761,RMVar_hsa_circ_282545,RMVar_hsa_circ_156464,RMVar_hsa_circ_156465 33682 RMVar_ID_33682 Human_SNP_ID_500856363 A-to-I Human chr12 + 50460870 50460870 50460870 GAGGCTGAGGCAGGAGAATGGCGTGAACCCGGAAGGCAGAGCTTGCAGTGAGCTGAGATGTGCCA GAGGCTGAGGCAGGAGAATGGCGTGAACCCGGGAGGCAGAGCTTGCAGTGAGCTGAGATGTGCCA A G LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs781294619 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_300058,RMVar_hsa_circ_362825,RMVar_hsa_circ_282759,RMVar_hsa_circ_65767,RMVar_hsa_circ_156431,RMVar_hsa_circ_284685,RMVar_hsa_circ_156442,RMVar_hsa_circ_65030,RMVar_hsa_circ_42887,RMVar_hsa_circ_350297,RMVar_hsa_circ_364298,RMVar_hsa_circ_340771,RMVar_hsa_circ_156443,RMVar_hsa_circ_333323,RMVar_hsa_circ_38780,RMVar_hsa_circ_56483,RMVar_hsa_circ_8813,RMVar_hsa_circ_343836,RMVar_hsa_circ_156451,RMVar_hsa_circ_8042,RMVar_hsa_circ_156459,RMVar_hsa_circ_156461,RMVar_hsa_circ_344696,RMVar_hsa_circ_320479,RMVar_hsa_circ_365181,RMVar_hsa_circ_315231,RMVar_hsa_circ_6366,RMVar_hsa_circ_156463,RMVar_hsa_circ_47930,RMVar_hsa_circ_310010,RMVar_hsa_circ_356162,RMVar_hsa_circ_337761,RMVar_hsa_circ_282545,RMVar_hsa_circ_156464,RMVar_hsa_circ_156465 33683 RMVar_ID_33683 Human_SNP_ID_500856364 A-to-I Human chr12 + 50460870 50460870 50460870 GAGGCTGAGGCAGGAGAATGGCGTGAACCCGGAAGGCAGAGCTTGCAGTGAGCTGAGATGTGCCA GAGGCTGAGGCAGGAGAATGGCGTGAACCCGGTAGGCAGAGCTTGCAGTGAGCTGAGATGTGCCA A T LARP4 Ensembl:ENSG00000161813 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs781294619 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_300058,RMVar_hsa_circ_362825,RMVar_hsa_circ_282759,RMVar_hsa_circ_65767,RMVar_hsa_circ_156431,RMVar_hsa_circ_284685,RMVar_hsa_circ_156442,RMVar_hsa_circ_65030,RMVar_hsa_circ_42887,RMVar_hsa_circ_350297,RMVar_hsa_circ_364298,RMVar_hsa_circ_340771,RMVar_hsa_circ_156443,RMVar_hsa_circ_333323,RMVar_hsa_circ_38780,RMVar_hsa_circ_56483,RMVar_hsa_circ_8813,RMVar_hsa_circ_343836,RMVar_hsa_circ_156451,RMVar_hsa_circ_8042,RMVar_hsa_circ_156459,RMVar_hsa_circ_156461,RMVar_hsa_circ_344696,RMVar_hsa_circ_320479,RMVar_hsa_circ_365181,RMVar_hsa_circ_315231,RMVar_hsa_circ_6366,RMVar_hsa_circ_156463,RMVar_hsa_circ_47930,RMVar_hsa_circ_310010,RMVar_hsa_circ_356162,RMVar_hsa_circ_337761,RMVar_hsa_circ_282545,RMVar_hsa_circ_156464,RMVar_hsa_circ_156465 33684 RMVar_ID_33684 Human_SNP_ID_500869656 A-to-I Human chr12 + 50511465 50511465 50511465 AGGCAAATGTCACTACCGTCTGGCTAATTTTTATATTTTTGGTAGAGACGGGGTTTCACTATGTT AGGCAAATGTCACTACCGTCTGGCTAATTTTTGTATTTTTGGTAGAGACGGGGTTTCACTATGTT A G DIP2B Ensembl:ENSG00000066084 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1180895592 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89229,RMVar_hsa_circ_156471 33685 RMVar_ID_33685 Human_SNP_ID_500870074 A-to-I Human chr12 + 50512948 50512948 50512948 AGAATTGCTTGAACCCGGGAGGCGGAGGTTGCAGTGAGCTAGGACCGCACCACTGCACTCCAGCC AGAATTGCTTGAACCCGGGAGGCGGAGGTTGCGGTGAGCTAGGACCGCACCACTGCACTCCAGCC A G DIP2B Ensembl:ENSG00000066084 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs548579661 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89229,RMVar_hsa_circ_156471 33686 RMVar_ID_33686 Human_SNP_ID_500871011 A-to-I Human chr12 + 50516528 50516521 50516529 CTCCCACCTTGGCCTCCCAAAGTGCAGAGATTATGACTGTGAGCCACTGTGCCTGGACCCCATCT CTCCCACCTTGGCCTCCCAAAGTGCA________GACTGTGAGCCACTGTGCCTGGACCCCATCT AGAGATTAT A DIP2B Ensembl:ENSG00000066084 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs758330055 Functional Loss DEL dbSNP153 27..34 33 - - - Human_RBP_ID_11964911 RMVar_hsa_circ_89229,RMVar_hsa_circ_156471 33687 RMVar_ID_33687 Human_SNP_ID_500871057 A-to-I Human chr12 + 50516717 50516717 50516717 TTTGTTTTGGCCGGACACGGTGGCTCATGCTTATAATCCCAGCACTTTGGGAGGCCAAGGTGGGC TTTGTTTTGGCCGGACACGGTGGCTCATGCTTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGC A G DIP2B Ensembl:ENSG00000066084 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559111963 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89229,RMVar_hsa_circ_156471 33688 RMVar_ID_33688 Human_SNP_ID_500873891 A-to-I Human chr12 + 50528067 50528067 50528067 CATCTGCCTTAGCCTCCCAGGTAGCTGAGACTACAAGCATGCACCACCATGCCCAGCTAGGTTTA CATCTGCCTTAGCCTCCCAGGTAGCTGAGACTGCAAGCATGCACCACCATGCCCAGCTAGGTTTA A G DIP2B Ensembl:ENSG00000066084 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs937166949 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89229,RMVar_hsa_circ_156471 33689 RMVar_ID_33689 Human_SNP_ID_500877324 A-to-I Human chr12 + 50541855 50541855 50541855 AAAACCCAGTCTACACTAAAAATACAAAAATTAGCCAGACGTGATGGCGTATGCCTGTAGTCCCA AAAACCCAGTCTACACTAAAAATACAAAAATTGGCCAGACGTGATGGCGTATGCCTGTAGTCCCA A G DIP2B Ensembl:ENSG00000066084 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs562418377 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11965508 RMVar_hsa_circ_89229,RMVar_hsa_circ_156471 33690 RMVar_ID_33690 Human_SNP_ID_500878117 A-to-I Human chr12 + 50544824 50544824 50544824 TATTTTTAGTAGAGAAGGGGTTCCACTGTGTTAGCCAGGCTGATCTCGAACTCCTGACCTCATGA TATTTTTAGTAGAGAAGGGGTTCCACTGTGTTGGCCAGGCTGATCTCGAACTCCTGACCTCATGA A G DIP2B Ensembl:ENSG00000066084 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1269260441 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89229,RMVar_hsa_circ_156471 33691 RMVar_ID_33691 Human_SNP_ID_500878158 A-to-I Human chr12 + 50544970 50544970 50544970 GAGTAGTACCAGGTGTGGTTTCTTATGACTGTAATACTAGCACTTTGGGAGGCCAAGATGGGAGA GAGTAGTACCAGGTGTGGTTTCTTATGACTGTGATACTAGCACTTTGGGAGGCCAAGATGGGAGA A G DIP2B Ensembl:ENSG00000066084 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1443124567 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2341686,Human_RBP_ID_5127125,Human_RBP_ID_17561114,Human_RBP_ID_22472325 RMVar_hsa_circ_89229,RMVar_hsa_circ_156471 33692 RMVar_ID_33692 Human_SNP_ID_500879034 A-to-I Human chr12 + 50548735 50548735 50548735 TTTAGTAGAGATGGGGTTTCGGCATGTTGGCCAGGCTGGTCTTGAACTCCTGACCTCAGGTAATT TTTAGTAGAGATGGGGTTTCGGCATGTTGGCCGGGCTGGTCTTGAACTCCTGACCTCAGGTAATT A G DIP2B Ensembl:ENSG00000066084 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1194132336 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89229,RMVar_hsa_circ_156471 33693 RMVar_ID_33693 Human_SNP_ID_500880671 A-to-I Human chr12 + 50555128 50555128 50555128 GGAATATAATATTCTTGCCCTCAACTCTTCCTAGTGTCCCCCATTCTAGAGACCCTCTGTTTGCC GGAATATAATATTCTTGCCCTCAACTCTTCCTGGTGTCCCCCATTCTAGAGACCCTCTGTTTGCC A G DIP2B Ensembl:ENSG00000066084 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs929780340 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89229,RMVar_hsa_circ_156471 33694 RMVar_ID_33694 Human_SNP_ID_500882243 A-to-I Human chr12 + 50561633 50561633 50561633 ATAAATTTGTTGTATTATTGATTGATTGAGACAGAGTCGCTTTGTTGCCTAGGCTGGAATGCAGT ATAAATTTGTTGTATTATTGATTGATTGAGACGGAGTCGCTTTGTTGCCTAGGCTGGAATGCAGT A G DIP2B Ensembl:ENSG00000066084 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935606262 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11965857 RMVar_hsa_circ_89229,RMVar_hsa_circ_156471 33695 RMVar_ID_33695 Human_SNP_ID_500884306 A-to-I Human chr12 + 50570644 50570644 50570644 AGGCGAGAGAATCACTTGAATCCGGGAGGCAGAAGTTACAATGAGCCGAGATCGCGCCACTGCGA AGGCGAGAGAATCACTTGAATCCGGGAGGCAGCAGTTACAATGAGCCGAGATCGCGCCACTGCGA A C DIP2B Ensembl:ENSG00000066084 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs961260895 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89229,RMVar_hsa_circ_156471 33696 RMVar_ID_33696 Human_SNP_ID_500899923 A-to-I Human chr12 + 50632757 50632757 50632757 CAAGGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTCCTGACCTCAAGTAATCCGCCTCCCTTC CAAGGTTTCACCATGTTGGCCAGGCTGGTCTCCAACTCCTGACCTCAAGTAATCCGCCTCCCTTC A C DIP2B Ensembl:ENSG00000066084 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs568977006 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107283,RMVar_hsa_circ_89229,RMVar_hsa_circ_156472,RMVar_hsa_circ_156471,RMVar_hsa_circ_296244,RMVar_hsa_circ_325458,RMVar_hsa_circ_156473,RMVar_hsa_circ_156474,RMVar_hsa_circ_156475 33697 RMVar_ID_33697 Human_SNP_ID_500899924 A-to-I Human chr12 + 50632757 50632757 50632757 CAAGGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTCCTGACCTCAAGTAATCCGCCTCCCTTC CAAGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAAGTAATCCGCCTCCCTTC A G DIP2B Ensembl:ENSG00000066084 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs568977006 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107283,RMVar_hsa_circ_89229,RMVar_hsa_circ_156472,RMVar_hsa_circ_156471,RMVar_hsa_circ_296244,RMVar_hsa_circ_325458,RMVar_hsa_circ_156473,RMVar_hsa_circ_156474,RMVar_hsa_circ_156475 33698 RMVar_ID_33698 Human_SNP_ID_500903249 A-to-I Human chr12 + 50647239 50647239 50647239 GCCTGGATGATTTTTGTATTTTTTGTGGAGACAGGGTTTCACCATGTTGCCTAAGCTGGAGTTTT GCCTGGATGATTTTTGTATTTTTTGTGGAGACGGGGTTTCACCATGTTGCCTAAGCTGGAGTTTT A G DIP2B Ensembl:ENSG00000066084 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1223608949 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107283,RMVar_hsa_circ_89229,RMVar_hsa_circ_156471,RMVar_hsa_circ_296244,RMVar_hsa_circ_76456,RMVar_hsa_circ_156474,RMVar_hsa_circ_156475,RMVar_hsa_circ_309964,RMVar_hsa_circ_361805,RMVar_hsa_circ_113109,RMVar_hsa_circ_156476,RMVar_hsa_circ_156477,RMVar_hsa_circ_156478 33699 RMVar_ID_33699 Human_SNP_ID_500905382 A-to-I Human chr12 + 50655809 50655809 50655809 TGAGAGCAACCTGGGCAACATAGTGAAACTCCATCTCTACCAAAAATACAAAAAATTAGCTGGGT TGAGAGCAACCTGGGCAACATAGTGAAACTCCGTCTCTACCAAAAATACAAAAAATTAGCTGGGT A G DIP2B Ensembl:ENSG00000066084 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992495551 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13638,RMVar_hsa_circ_107283,RMVar_hsa_circ_89229,RMVar_hsa_circ_156471,RMVar_hsa_circ_296244,RMVar_hsa_circ_76456,RMVar_hsa_circ_156474,RMVar_hsa_circ_156475,RMVar_hsa_circ_309964,RMVar_hsa_circ_361805,RMVar_hsa_circ_113109,RMVar_hsa_circ_156476,RMVar_hsa_circ_156477,RMVar_hsa_circ_156478,RMVar_hsa_circ_105838,RMVar_hsa_circ_156479 33700 RMVar_ID_33700 Human_SNP_ID_500918559 A-to-I Human chr12 + 50712340 50712340 50712340 AGTTGGTCAGTTTTAGCCAGGCATGATGGCTCATGTCTGTAATCCCAGCACTTTGGGAGGCCGAG AGTTGGTCAGTTTTAGCCAGGCATGATGGCTCCTGTCTGTAATCCCAGCACTTTGGGAGGCCGAG A C DIP2B Ensembl:ENSG00000066084 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs920076172 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107283,RMVar_hsa_circ_156475,RMVar_hsa_circ_110970,RMVar_hsa_circ_37183,RMVar_hsa_circ_33446,RMVar_hsa_circ_156490,RMVar_hsa_circ_268262,RMVar_hsa_circ_265421,RMVar_hsa_circ_266917,RMVar_hsa_circ_264861,RMVar_hsa_circ_31160,RMVar_hsa_circ_49631,RMVar_hsa_circ_331582,RMVar_hsa_circ_363688,RMVar_hsa_circ_323755,RMVar_hsa_circ_53409,RMVar_hsa_circ_156495,RMVar_hsa_circ_31651,RMVar_hsa_circ_35419,RMVar_hsa_circ_80709,RMVar_hsa_circ_156494,RMVar_hsa_circ_79172,RMVar_hsa_circ_156501,RMVar_hsa_circ_115873,RMVar_hsa_circ_17957,RMVar_hsa_circ_156506,RMVar_hsa_circ_156507,RMVar_hsa_circ_156505,RMVar_hsa_circ_38090,RMVar_hsa_circ_67944,RMVar_hsa_circ_268763,RMVar_hsa_circ_362418,RMVar_hsa_circ_89475,RMVar_hsa_circ_156509,RMVar_hsa_circ_156510,RMVar_hsa_circ_329117,RMVar_hsa_circ_92985,RMVar_hsa_circ_156511,RMVar_hsa_circ_18791,RMVar_hsa_circ_8939,RMVar_hsa_circ_338429,RMVar_hsa_circ_156512,RMVar_hsa_circ_324735,RMVar_hsa_circ_306589 33701 RMVar_ID_33701 Human_SNP_ID_500918560 A-to-I Human chr12 + 50712340 50712340 50712340 AGTTGGTCAGTTTTAGCCAGGCATGATGGCTCATGTCTGTAATCCCAGCACTTTGGGAGGCCGAG AGTTGGTCAGTTTTAGCCAGGCATGATGGCTCGTGTCTGTAATCCCAGCACTTTGGGAGGCCGAG A G DIP2B Ensembl:ENSG00000066084 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs920076172 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107283,RMVar_hsa_circ_156475,RMVar_hsa_circ_110970,RMVar_hsa_circ_37183,RMVar_hsa_circ_33446,RMVar_hsa_circ_156490,RMVar_hsa_circ_268262,RMVar_hsa_circ_265421,RMVar_hsa_circ_266917,RMVar_hsa_circ_264861,RMVar_hsa_circ_31160,RMVar_hsa_circ_49631,RMVar_hsa_circ_331582,RMVar_hsa_circ_363688,RMVar_hsa_circ_323755,RMVar_hsa_circ_53409,RMVar_hsa_circ_156495,RMVar_hsa_circ_31651,RMVar_hsa_circ_35419,RMVar_hsa_circ_80709,RMVar_hsa_circ_156494,RMVar_hsa_circ_79172,RMVar_hsa_circ_156501,RMVar_hsa_circ_115873,RMVar_hsa_circ_17957,RMVar_hsa_circ_156506,RMVar_hsa_circ_156507,RMVar_hsa_circ_156505,RMVar_hsa_circ_38090,RMVar_hsa_circ_67944,RMVar_hsa_circ_268763,RMVar_hsa_circ_362418,RMVar_hsa_circ_89475,RMVar_hsa_circ_156509,RMVar_hsa_circ_156510,RMVar_hsa_circ_329117,RMVar_hsa_circ_92985,RMVar_hsa_circ_156511,RMVar_hsa_circ_18791,RMVar_hsa_circ_8939,RMVar_hsa_circ_338429,RMVar_hsa_circ_156512,RMVar_hsa_circ_324735,RMVar_hsa_circ_306589 33702 RMVar_ID_33702 Human_SNP_ID_500918756 A-to-I Human chr12 + 50713209 50713209 50713209 AACTCAAACTGTCTTCTCACCTTGGCCTCCCAAAGTGCTGAGATTACAGACTTGAGTCACCATAC AACTCAAACTGTCTTCTCACCTTGGCCTCCCAGAGTGCTGAGATTACAGACTTGAGTCACCATAC A G DIP2B Ensembl:ENSG00000066084 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1025983315 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107283,RMVar_hsa_circ_156475,RMVar_hsa_circ_110970,RMVar_hsa_circ_37183,RMVar_hsa_circ_33446,RMVar_hsa_circ_156490,RMVar_hsa_circ_268262,RMVar_hsa_circ_265421,RMVar_hsa_circ_266917,RMVar_hsa_circ_264861,RMVar_hsa_circ_31160,RMVar_hsa_circ_49631,RMVar_hsa_circ_331582,RMVar_hsa_circ_363688,RMVar_hsa_circ_323755,RMVar_hsa_circ_53409,RMVar_hsa_circ_156495,RMVar_hsa_circ_31651,RMVar_hsa_circ_35419,RMVar_hsa_circ_80709,RMVar_hsa_circ_156494,RMVar_hsa_circ_79172,RMVar_hsa_circ_156501,RMVar_hsa_circ_115873,RMVar_hsa_circ_17957,RMVar_hsa_circ_156506,RMVar_hsa_circ_156507,RMVar_hsa_circ_156505,RMVar_hsa_circ_38090,RMVar_hsa_circ_67944,RMVar_hsa_circ_268763,RMVar_hsa_circ_362418,RMVar_hsa_circ_89475,RMVar_hsa_circ_156509,RMVar_hsa_circ_156510,RMVar_hsa_circ_329117,RMVar_hsa_circ_92985,RMVar_hsa_circ_156511,RMVar_hsa_circ_18791,RMVar_hsa_circ_8939,RMVar_hsa_circ_338429,RMVar_hsa_circ_156512,RMVar_hsa_circ_324735,RMVar_hsa_circ_306589 33703 RMVar_ID_33703 Human_SNP_ID_500918758 A-to-I Human chr12 + 50713222 50713222 50713222 TTCTCACCTTGGCCTCCCAAAGTGCTGAGATTACAGACTTGAGTCACCATACCCGGCCTGGTTTT TTCTCACCTTGGCCTCCCAAAGTGCTGAGATTTCAGACTTGAGTCACCATACCCGGCCTGGTTTT A T DIP2B Ensembl:ENSG00000066084 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1208998496 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107283,RMVar_hsa_circ_156475,RMVar_hsa_circ_110970,RMVar_hsa_circ_37183,RMVar_hsa_circ_33446,RMVar_hsa_circ_156490,RMVar_hsa_circ_268262,RMVar_hsa_circ_265421,RMVar_hsa_circ_266917,RMVar_hsa_circ_264861,RMVar_hsa_circ_31160,RMVar_hsa_circ_49631,RMVar_hsa_circ_331582,RMVar_hsa_circ_363688,RMVar_hsa_circ_323755,RMVar_hsa_circ_53409,RMVar_hsa_circ_156495,RMVar_hsa_circ_31651,RMVar_hsa_circ_35419,RMVar_hsa_circ_80709,RMVar_hsa_circ_156494,RMVar_hsa_circ_79172,RMVar_hsa_circ_156501,RMVar_hsa_circ_115873,RMVar_hsa_circ_17957,RMVar_hsa_circ_156506,RMVar_hsa_circ_156507,RMVar_hsa_circ_156505,RMVar_hsa_circ_38090,RMVar_hsa_circ_67944,RMVar_hsa_circ_268763,RMVar_hsa_circ_362418,RMVar_hsa_circ_89475,RMVar_hsa_circ_156509,RMVar_hsa_circ_156510,RMVar_hsa_circ_329117,RMVar_hsa_circ_92985,RMVar_hsa_circ_156511,RMVar_hsa_circ_18791,RMVar_hsa_circ_8939,RMVar_hsa_circ_338429,RMVar_hsa_circ_156512,RMVar_hsa_circ_324735,RMVar_hsa_circ_306589 33704 RMVar_ID_33704 Human_SNP_ID_500927923 A-to-I Human chr12 + 50751706 50751706 50751706 ACAGCATTTAAAGGTTCGTGAGGGCCGGGCACAATGGCTCATGCCTGTAATCCCAGCACTTTGGG ACAGCATTTAAAGGTTCGTGAGGGCCGGGCACGATGGCTCATGCCTGTAATCCCAGCACTTTGGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1375642927 Functional Loss SNV dbSNP153 33..33 33 - - - 33705 RMVar_ID_33705 Human_SNP_ID_500930730 A-to-I Human chr12 - 50762145 50762145 50762145 GAAACCCCGTCTCTACTAAAAATACAAAAATTAGCCAGGTGTGGTGGCACACACCTGTAATCCCA GAAACCCCGTCTCTACTAAAAATACAAAAATTCGCCAGGTGTGGTGGCACACACCTGTAATCCCA T G lnc-SLC11A2-8,lnc-SLC11A2-7,lnc-SLC11A2-7:2 RNACentral:URS0000D5E087,RNACentral:URS0000D5ACD2,RNACentral:URS0000D56D46 lincRNA,lincRNA,lincRNA intron,exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1249976948 Functional Loss SNV dbSNP153 33..33 33 - - - 33706 RMVar_ID_33706 Human_SNP_ID_500931110 A-to-I Human chr12 - 50763532 50763532 50763532 CGACTCACTGCAGCCTCCAACCCCGGGATTCAAGCGATTCTCCAACCTCAGCCTATGGGGCAGCT CGACTCACTGCAGCCTCCAACCCCGGGATTCAGGCGATTCTCCAACCTCAGCCTATGGGGCAGCT T C lnc-SLC11A2-8,lnc-SLC11A2-7,lnc-SLC11A2-7:2 RNACentral:URS0000D5E087,RNACentral:URS0000D5ACD2,RNACentral:URS0000D56D46 lincRNA,lincRNA,lincRNA intron,exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs573957587 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27422681 33707 RMVar_ID_33707 Human_SNP_ID_500931111 A-to-I Human chr12 - 50763532 50763532 50763532 CGACTCACTGCAGCCTCCAACCCCGGGATTCAAGCGATTCTCCAACCTCAGCCTATGGGGCAGCT CGACTCACTGCAGCCTCCAACCCCGGGATTCACGCGATTCTCCAACCTCAGCCTATGGGGCAGCT T G lnc-SLC11A2-8,lnc-SLC11A2-7,lnc-SLC11A2-7:2 RNACentral:URS0000D5E087,RNACentral:URS0000D5ACD2,RNACentral:URS0000D56D46 lincRNA,lincRNA,lincRNA intron,exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs573957587 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27422681 33708 RMVar_ID_33708 Human_SNP_ID_500932452 A-to-I Human chr12 + 50767947 50767947 50767947 CAGGCTGGAGTGCAGTGGTGCGATCTCAGCTCACTGCAACCTCCGCCTCCCGAGTTCAAGTGATT CAGGCTGGAGTGCAGTGGTGCGATCTCAGCTCGCTGCAACCTCCGCCTCCCGAGTTCAAGTGATT A G ATF1 Ensembl:ENSG00000123268 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1414227606 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93027,RMVar_hsa_circ_156530 33709 RMVar_ID_33709 Human_SNP_ID_500934438 A-to-I Human chr12 + 50775951 50775951 50775951 GTGTGGCTGATGGCCTGTAATCGCAACACTTTAGGAGGCCAAGGTAGGTGGATCGTTTGAGCTTA GTGTGGCTGATGGCCTGTAATCGCAACACTTTGGGAGGCCAAGGTAGGTGGATCGTTTGAGCTTA A G ATF1 Ensembl:ENSG00000123268 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs989109457 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44846,RMVar_hsa_circ_93027,RMVar_hsa_circ_156530 33710 RMVar_ID_33710 Human_SNP_ID_500939795 A-to-I Human chr12 + 50797668 50797668 50797668 TTTTTTTTAATTTTTGGTAGAGATAGAGTCCCACTATGTTGACCAGGCTGGTGTCAAACTCTTGG TTTTTTTTAATTTTTGGTAGAGATAGAGTCCCCCTATGTTGACCAGGCTGGTGTCAAACTCTTGG A C ATF1 Ensembl:ENSG00000123268 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs368446420 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93027,RMVar_hsa_circ_156530,RMVar_hsa_circ_156532,RMVar_hsa_circ_268278,RMVar_hsa_circ_285069,RMVar_hsa_circ_272820,RMVar_hsa_circ_156533,RMVar_hsa_circ_349574,RMVar_hsa_circ_304440,RMVar_hsa_circ_156535,RMVar_hsa_circ_156536 33711 RMVar_ID_33711 Human_SNP_ID_500939798 A-to-I Human chr12 + 50797705 50797705 50797705 GTTGACCAGGCTGGTGTCAAACTCTTGGGCTCAAGTGATCCTCCCACCTCAGCCTCCCAAAGTGT GTTGACCAGGCTGGTGTCAAACTCTTGGGCTCGAGTGATCCTCCCACCTCAGCCTCCCAAAGTGT A G ATF1 Ensembl:ENSG00000123268 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1241285558 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93027,RMVar_hsa_circ_156530,RMVar_hsa_circ_156532,RMVar_hsa_circ_268278,RMVar_hsa_circ_285069,RMVar_hsa_circ_272820,RMVar_hsa_circ_156533,RMVar_hsa_circ_349574,RMVar_hsa_circ_304440,RMVar_hsa_circ_156535,RMVar_hsa_circ_156536 33712 RMVar_ID_33712 Human_SNP_ID_500941865 A-to-I Human chr12 + 50807282 50807264 50807282 AAAAAATTAGCCAGGTATGATGGCGTGTACCTATATTCCCAGCTGCTTGGGAGGCTGAGGCAGGA AAAAAATTAGCCAGG__________________TATTCCCAGCTGCTTGGGAGGCTGAGGCAGGA GTATGATGGCGTGTACCTA G ATF1 Ensembl:ENSG00000123268 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1480253787 Functional Loss DEL dbSNP153 16..33 33 - - - RMVar_hsa_circ_93027,RMVar_hsa_circ_156530,RMVar_hsa_circ_156532,RMVar_hsa_circ_268278,RMVar_hsa_circ_285069,RMVar_hsa_circ_272820,RMVar_hsa_circ_156533,RMVar_hsa_circ_349574,RMVar_hsa_circ_304440,RMVar_hsa_circ_156535,RMVar_hsa_circ_156536 33713 RMVar_ID_33713 Human_SNP_ID_500941873 A-to-I Human chr12 + 50807282 50807282 50807282 AAAAAATTAGCCAGGTATGATGGCGTGTACCTATATTCCCAGCTGCTTGGGAGGCTGAGGCAGGA AAAAAATTAGCCAGGTATGATGGCGTGTACCTGTATTCCCAGCTGCTTGGGAGGCTGAGGCAGGA A G ATF1 Ensembl:ENSG00000123268 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1438780425 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93027,RMVar_hsa_circ_156530,RMVar_hsa_circ_156532,RMVar_hsa_circ_268278,RMVar_hsa_circ_285069,RMVar_hsa_circ_272820,RMVar_hsa_circ_156533,RMVar_hsa_circ_349574,RMVar_hsa_circ_304440,RMVar_hsa_circ_156535,RMVar_hsa_circ_156536 33714 RMVar_ID_33714 Human_SNP_ID_500944570 A-to-I Human chr12 + 50818351 50818351 50818351 GGGATATCTTGAGTCCAGGAGGTCAAGGTTGCAATGAGCTGTGATTGTGCCACTGCACTCAGCCT GGGATATCTTGAGTCCAGGAGGTCAAGGTTGCGATGAGCTGTGATTGTGCCACTGCACTCAGCCT A G ATF1 Ensembl:ENSG00000123268 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs988808214 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268278 33715 RMVar_ID_33715 Human_SNP_ID_500944648 A-to-I Human chr12 + 50818755 50818755 50818755 GGTCAGACTCCCAAGTAGCTGGGATTACAGGCATGTGCCACCACAGCTAATTTTTGTATTTTTAG GGTCAGACTCCCAAGTAGCTGGGATTACAGGCGTGTGCCACCACAGCTAATTTTTGTATTTTTAG A G ATF1 Ensembl:ENSG00000123268 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs148893489 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268278 33716 RMVar_ID_33716 Human_SNP_ID_500945001 A-to-I Human chr12 + 50820237 50820237 50820237 AAATTCTAAATTACAAAGGTAAGAGAAAACCTAGTACATTACTAAATATATAAAGTATATGTTCT AAATTCTAAATTACAAAGGTAAGAGAAAACCTGGTACATTACTAAATATATAAAGTATATGTTCT A G ATF1 Ensembl:ENSG00000123268 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1467144201 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_992792,Human_RBP_ID_2342142,Human_RBP_ID_17821135,Human_RBP_ID_26613060,Human_RBP_ID_27630223 RMVar_hsa_circ_268278 33717 RMVar_ID_33717 Human_SNP_ID_500971200 A-to-I Human chr12 + 50930339 50930339 50930339 TTTGCTCTTGTTGCCCAGGCTGGAGTGCAATGACGTGATCTCCGCTCACTGCAACCTCCACCTCG TTTGCTCTTGTTGCCCAGGCTGGAGTGCAATGCCGTGATCTCCGCTCACTGCAACCTCCACCTCG A C METTL7A Ensembl:ENSG00000185432 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,29129909,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs1170377666 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1368823 33718 RMVar_ID_33718 Human_SNP_ID_500971202 A-to-I Human chr12 + 50930344 50930344 50930344 TCTTGTTGCCCAGGCTGGAGTGCAATGACGTGATCTCCGCTCACTGCAACCTCCACCTCGCGGGT TCTTGTTGCCCAGGCTGGAGTGCAATGACGTGTTCTCCGCTCACTGCAACCTCCACCTCGCGGGT A T METTL7A Ensembl:ENSG00000185432 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1196072733 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4226926 Human_Splice_Rec_1368823 33719 RMVar_ID_33719 Human_SNP_ID_500971210 A-to-I Human chr12 + 50930366 50930366 50930366 CAATGACGTGATCTCCGCTCACTGCAACCTCCACCTCGCGGGTTTAAGCGATTCTTCTGCCTCAG CAATGACGTGATCTCCGCTCACTGCAACCTCCGCCTCGCGGGTTTAAGCGATTCTTCTGCCTCAG A G METTL7A Ensembl:ENSG00000185432 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs565829859 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1368823 33720 RMVar_ID_33720 Human_SNP_ID_500971231 A-to-I Human chr12 + 50930409 50930409 50930409 TTAAGCGATTCTTCTGCCTCAGCCTCCCTAGTAGCTGGGATTACAGGTGCCCACCACCATGCCCA TTAAGCGATTCTTCTGCCTCAGCCTCCCTAGTGGCTGGGATTACAGGTGCCCACCACCATGCCCA A G METTL7A Ensembl:ENSG00000185432 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE107867;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;ASD brains,cerebellum;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,29129909,30559470,31158229,32596459 RNA-Seq:(High) rs1176040353 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1368823 33721 RMVar_ID_33721 Human_SNP_ID_500971235 A-to-I Human chr12 + 50930419 50930419 50930419 CTTCTGCCTCAGCCTCCCTAGTAGCTGGGATTACAGGTGCCCACCACCATGCCCAGCTAATTTGT CTTCTGCCTCAGCCTCCCTAGTAGCTGGGATTGCAGGTGCCCACCACCATGCCCAGCTAATTTGT A G METTL7A Ensembl:ENSG00000185432 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 23474544,24183664,29129909,31158229 RNA-Seq:(High) rs1238121802 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1368823 33722 RMVar_ID_33722 Human_SNP_ID_500971252 A-to-I Human chr12 + 50930487 50930487 50930487 TTTAGTTGAGACAGGGTTTCACTACGTTGGCCAGGCTGGTCTTGAACTCCTGATCTCAGGCAATC TTTAGTTGAGACAGGGTTTCACTACGTTGGCCGGGCTGGTCTTGAACTCCTGATCTCAGGCAATC A G METTL7A Ensembl:ENSG00000185432 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560067365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_421654,Human_RBP_ID_8178557,Human_RBP_ID_22369816,Human_RBP_ID_26416869,Human_RBP_ID_27630244 33723 RMVar_ID_33723 Human_SNP_ID_500971260 A-to-I Human chr12 + 50930530 50930530 50930530 GAACTCCTGATCTCAGGCAATCCACCCACCTCAGCCTCCCAAAGTGCTGGGATGACAGGCGTGAG GAACTCCTGATCTCAGGCAATCCACCCACCTCCGCCTCCCAAAGTGCTGGGATGACAGGCGTGAG A C METTL7A Ensembl:ENSG00000185432 Protein coding 3'UTR GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs937391251 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8178558 33724 RMVar_ID_33724 Human_SNP_ID_500971287 A-to-I Human chr12 + 50930658 50930658 50930658 CAGGCTGGAGTGCAATGCTGTGATCTCAGCTTACCACAACCTCCACCTCCCGGGTTCAAGTGATT CAGGCTGGAGTGCAATGCTGTGATCTCAGCTTGCCACAACCTCCACCTCCCGGGTTCAAGTGATT A G METTL7A Ensembl:ENSG00000185432 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1007887261 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8178562,Human_RBP_ID_22369817 33725 RMVar_ID_33725 Human_SNP_ID_500971298 A-to-I Human chr12 + 50930723 50930723 50930723 CACCTGCCTCAGCCTCCTGAGTAGCTGGTATTACAGGCATGCGTCACCACGCCGGCTAATTTTGT CACCTGCCTCAGCCTCCTGAGTAGCTGGTATTGCAGGCATGCGTCACCACGCCGGCTAATTTTGT A G METTL7A Ensembl:ENSG00000185432 Protein coding 3'UTR GSE38233;GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,30559470,31158229 RNA-Seq:(High) rs1475399000 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6194077,Human_RBP_ID_8178564,Human_RBP_ID_17561120,Human_RBP_ID_26421189 Human_miRNA_ID_604469,Human_miRNA_ID_1398879 33726 RMVar_ID_33726 Human_SNP_ID_500971308 A-to-I Human chr12 + 50930762 50930760 50930763 TGCGTCACCACGCCGGCTAATTTTGTACTTTTAGTAGAGATGGTGTTTCCCCACGTTGGTCAGTC TGCGTCACCACGCCGGCTAATTTTGTACTTT___TAGAGATGGTGTTTCCCCACGTTGGTCAGTC TTAG T METTL7A Ensembl:ENSG00000185432 Protein coding 3'UTR GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs1340295986 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_11967634,Human_RBP_ID_17561120,Human_RBP_ID_18261249,Human_RBP_ID_21885181,Human_RBP_ID_26416872 33727 RMVar_ID_33727 Human_SNP_ID_500971480 A-to-I Human chr12 + 50931454 50931454 50931454 ACAGGGGGCTGGGCGTGGTGGCTCACGCCTGTAATCCTAGCACTTTGGGAGGCCGAGGCGGGTGG ACAGGGGGCTGGGCGTGGTGGCTCACGCCTGTGATCCTAGCACTTTGGGAGGCCGAGGCGGGTGG A G METTL7A Ensembl:ENSG00000185432 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs3180343 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8178574,Human_RBP_ID_26422213 33728 RMVar_ID_33728 Human_SNP_ID_500971505 A-to-I Human chr12 + 50931504 50931504 50931504 GGCCGAGGCGGGTGGATCACGAGGTAGGAGTTAAAGACCAGCCTGGCCAACATGGCAAAACCCTA GGCCGAGGCGGGTGGATCACGAGGTAGGAGTTGAAGACCAGCCTGGCCAACATGGCAAAACCCTA A G METTL7A Ensembl:ENSG00000185432 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs3180345 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8177928,Human_RBP_ID_26421196 33729 RMVar_ID_33729 Human_SNP_ID_500971520 A-to-I Human chr12 + 50931564 50931564 50931564 CCCTACTAAAGATACAAAAAAAAAAAAAAATTAGCCAGGCGTGGTGGTGGGTGCCTGTAATCCCA CCCTACTAAAGATACAAAAAAAAAAAAAAATTGGCCAGGCGTGGTGGTGGGTGCCTGTAATCCCA A G METTL7A Ensembl:ENSG00000185432 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1293174705 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26416893 33730 RMVar_ID_33730 Human_SNP_ID_500971521 A-to-I Human chr12 + 50931564 50931564 50931564 CCCTACTAAAGATACAAAAAAAAAAAAAAATTAGCCAGGCGTGGTGGTGGGTGCCTGTAATCCCA CCCTACTAAAGATACAAAAAAAAAAAAAAATTTGCCAGGCGTGGTGGTGGGTGCCTGTAATCCCA A T METTL7A Ensembl:ENSG00000185432 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1293174705 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26416893 33731 RMVar_ID_33731 Human_SNP_ID_500971524 A-to-I Human chr12 + 50931568 50931568 50931568 ACTAAAGATACAAAAAAAAAAAAAAATTAGCCAGGCGTGGTGGTGGGTGCCTGTAATCCCAGGTA ACTAAAGATACAAAAAAAAAAAAAAATTAGCCGGGCGTGGTGGTGGGTGCCTGTAATCCCAGGTA A G METTL7A Ensembl:ENSG00000185432 Protein coding 3'UTR GSE38233;GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,32596459 RNA-Seq:(High) rs1449225128 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26416893 33732 RMVar_ID_33732 Human_SNP_ID_500971535 A-to-I Human chr12 + 50931596 50931596 50931596 AGCCAGGCGTGGTGGTGGGTGCCTGTAATCCCAGGTACTTGGAAGGCTGAGGCAGGAGAATCTCT AGCCAGGCGTGGTGGTGGGTGCCTGTAATCCCGGGTACTTGGAAGGCTGAGGCAGGAGAATCTCT A G METTL7A Ensembl:ENSG00000185432 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs3180986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8178576,Human_RBP_ID_17561121 33733 RMVar_ID_33733 Human_SNP_ID_500971549 A-to-I Human chr12 + 50931652 50931652 50931652 AGAATCTCTTGAACCCAGAAGGCGAAGGTTGCAGTGAACCGAGATCATGCCATTGTACTCTAGCC AGAATCTCTTGAACCCAGAAGGCGAAGGTTGCCGTGAACCGAGATCATGCCATTGTACTCTAGCC A C METTL7A Ensembl:ENSG00000185432 Protein coding 3'UTR GSE38233;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,32596459 RNA-Seq:(High) rs1210260263 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8178577,Human_RBP_ID_17561121,Human_RBP_ID_26416894 Human_Splice_Rec_1368824 33734 RMVar_ID_33734 Human_SNP_ID_500971555 A-to-I Human chr12 + 50931666 50931666 50931666 CCAGAAGGCGAAGGTTGCAGTGAACCGAGATCATGCCATTGTACTCTAGCCTGGGTGACAAGAGC CCAGAAGGCGAAGGTTGCAGTGAACCGAGATCGTGCCATTGTACTCTAGCCTGGGTGACAAGAGC A G METTL7A Ensembl:ENSG00000185432 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs958965881 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17561122 Human_Splice_Rec_1368824 33735 RMVar_ID_33735 Human_SNP_ID_500971557 A-to-I Human chr12 + 50931671 50931671 50931671 AGGCGAAGGTTGCAGTGAACCGAGATCATGCCATTGTACTCTAGCCTGGGTGACAAGAGCAAGAC AGGCGAAGGTTGCAGTGAACCGAGATCATGCCGTTGTACTCTAGCCTGGGTGACAAGAGCAAGAC A G METTL7A Ensembl:ENSG00000185432 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs377657191 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17561122 Human_Splice_Rec_1368824 33736 RMVar_ID_33736 Human_SNP_ID_500971563 A-to-I Human chr12 + 50931693 50931693 50931693 AGATCATGCCATTGTACTCTAGCCTGGGTGACAAGAGCAAGACTCCGTCTCAAAAAAAAAAAAAA AGATCATGCCATTGTACTCTAGCCTGGGTGACGAGAGCAAGACTCCGTCTCAAAAAAAAAAAAAA A G METTL7A Ensembl:ENSG00000185432 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1418575727 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17561122 Human_Splice_Rec_1368824 33737 RMVar_ID_33737 Human_SNP_ID_500971606 A-to-I Human chr12 + 50931754 50931754 50931754 AAAAAAAAAAAAAGAAGTAGAGACAGGGAGACAGGGTCTCACTGTGTTGCCTAGGCCGGTCTTGA AAAAAAAAAAAAAGAAGTAGAGACAGGGAGACGGGGTCTCACTGTGTTGCCTAGGCCGGTCTTGA A G METTL7A Ensembl:ENSG00000185432 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs3180347 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6194094,Human_RBP_ID_8178578,Human_RBP_ID_26421197 Human_miRNA_ID_75631,Human_miRNA_ID_78801,Human_miRNA_ID_975433,Human_miRNA_ID_1079978 33738 RMVar_ID_33738 Human_SNP_ID_500971616 A-to-I Human chr12 + 50931799 50931799 50931799 GTTGCCTAGGCCGGTCTTGAACTCCTGGGCTCAAGTGATTCTCCCACCTTGACCTCCTAAATTGT GTTGCCTAGGCCGGTCTTGAACTCCTGGGCTCCAGTGATTCTCCCACCTTGACCTCCTAAATTGT A C METTL7A Ensembl:ENSG00000185432 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs539284466 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_421658,Human_RBP_ID_4255986 Human_miRNA_ID_1038805 33739 RMVar_ID_33739 Human_SNP_ID_500979974 A-to-I Human chr12 - 50967916 50967916 50967916 GCCTGGCTAACTTTTTAATTTTTTGTAGAGATAGGGTATTCGCCATGTTGCCCAGAATGGTCTCA GCCTGGCTAACTTTTTAATTTTTTGTAGAGATTGGGTATTCGCCATGTTGCCCAGAATGGTCTCA T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251241184 Functional Loss SNV dbSNP153 33..33 33 - - - 33740 RMVar_ID_33740 Human_SNP_ID_500989331 A-to-I Human chr12 - 51006260 51006260 51006260 AGTTTCACTCTTGTCGCCCAGGCTAGAGTGCAATGGTGCAATCCTGGCTCACCGCAACCTCCTCC AGTTTCACTCTTGTCGCCCAGGCTAGAGTGCAGTGGTGCAATCCTGGCTCACCGCAACCTCCTCC T C SLC11A2 Ensembl:ENSG00000110911 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs974601727 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1369322 RMVar_hsa_circ_299421,RMVar_hsa_circ_156541,RMVar_hsa_circ_272864,RMVar_hsa_circ_156543,RMVar_hsa_circ_323416,RMVar_hsa_circ_346139,RMVar_hsa_circ_156547,RMVar_hsa_circ_282237,RMVar_hsa_circ_106885,RMVar_hsa_circ_156550,RMVar_hsa_circ_156551,RMVar_hsa_circ_319932,RMVar_hsa_circ_59148,RMVar_hsa_circ_156552,RMVar_hsa_circ_330402,RMVar_hsa_circ_273619,RMVar_hsa_circ_156553 33741 RMVar_ID_33741 Human_SNP_ID_500989725 A-to-I Human chr12 - 51008093 51008093 51008093 TCAAGTGATTCTCCCACTTCAGCCTCCCCAGTAGCTGGGACTATAGATGGCATGCCACCATGCCA TCAAGTGATTCTCCCACTTCAGCCTCCCCAGTTGCTGGGACTATAGATGGCATGCCACCATGCCA T A SLC11A2 Ensembl:ENSG00000110911 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355703330 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_299421,RMVar_hsa_circ_156541,RMVar_hsa_circ_272864,RMVar_hsa_circ_156543,RMVar_hsa_circ_323416,RMVar_hsa_circ_346139,RMVar_hsa_circ_156547,RMVar_hsa_circ_282237,RMVar_hsa_circ_106885,RMVar_hsa_circ_156550,RMVar_hsa_circ_156551,RMVar_hsa_circ_319932,RMVar_hsa_circ_59148,RMVar_hsa_circ_156552,RMVar_hsa_circ_330402,RMVar_hsa_circ_273619,RMVar_hsa_circ_156553 33742 RMVar_ID_33742 Human_SNP_ID_500989737 A-to-I Human chr12 - 51008153 51008153 51008153 TCATCTAGGCTCCAGTGCAGTGGCACAACCATAGCCCACTGTAGCCTTGAATTCCTGGGGTCAAG TCATCTAGGCTCCAGTGCAGTGGCACAACCATGGCCCACTGTAGCCTTGAATTCCTGGGGTCAAG T C SLC11A2 Ensembl:ENSG00000110911 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs920293744 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11968042,Human_RBP_ID_19778947 RMVar_hsa_circ_299421,RMVar_hsa_circ_156541,RMVar_hsa_circ_272864,RMVar_hsa_circ_156543,RMVar_hsa_circ_323416,RMVar_hsa_circ_346139,RMVar_hsa_circ_156547,RMVar_hsa_circ_282237,RMVar_hsa_circ_106885,RMVar_hsa_circ_156550,RMVar_hsa_circ_156551,RMVar_hsa_circ_319932,RMVar_hsa_circ_59148,RMVar_hsa_circ_156552,RMVar_hsa_circ_330402,RMVar_hsa_circ_273619,RMVar_hsa_circ_156553 33743 RMVar_ID_33743 Human_SNP_ID_500991917 A-to-I Human chr12 - 51016150 51016150 51016150 GCAATCTGCCTGCCTTGGCCTCCCGAAGTGTTAGGATTACAGGCATGAGCCACTACAGCCAGCCA GCAATCTGCCTGCCTTGGCCTCCCGAAGTGTTGGGATTACAGGCATGAGCCACTACAGCCAGCCA T C SLC11A2 Ensembl:ENSG00000110911 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs901846811 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18918 33744 RMVar_ID_33744 Human_SNP_ID_500992575 A-to-I Human chr12 - 51018757 51018757 51018757 TTTATTTATTTATTTATTTGTTTATGACAGACAGGGTCTTGCTCTGTAGCCCAGGCTGGGGTGCC TTTATTTATTTATTTATTTGTTTATGACAGACGGGGTCTTGCTCTGTAGCCCAGGCTGGGGTGCC T C SLC11A2 Ensembl:ENSG00000110911 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348122859 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6194252 RMVar_hsa_circ_18918 33745 RMVar_ID_33745 Human_SNP_ID_500992897 A-to-I Human chr12 - 51020199 51020199 51020199 AAAAAAAGCCAGCTGTGGTGGTACGTGCCTGTAGTCTCAGCTACTTGGGAACTTGGGAGGCTGAG AAAAAAAGCCAGCTGTGGTGGTACGTGCCTGTTGTCTCAGCTACTTGGGAACTTGGGAGGCTGAG T A SLC11A2 Ensembl:ENSG00000110911 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404379624 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17561125 RMVar_hsa_circ_18918 33746 RMVar_ID_33746 Human_SNP_ID_501000286 A-to-I Human chr12 + 51049940 51049940 51049940 ATTTTCATCTAAATGTTACCTAACAGTATTATAAGTTGGTGCAAAAGTAATTGCGGCTTTTGGCT ATTTTCATCTAAATGTTACCTAACAGTATTATGAGTTGGTGCAAAAGTAATTGCGGCTTTTGGCT A G LETMD1 Ensembl:ENSG00000050426 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1040780468 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3549,RMVar_hsa_circ_332234,RMVar_hsa_circ_24451,RMVar_hsa_circ_276574,RMVar_hsa_circ_280689,RMVar_hsa_circ_99391,RMVar_hsa_circ_156557,RMVar_hsa_circ_156558,RMVar_hsa_circ_156556 33747 RMVar_ID_33747 Human_SNP_ID_501000365 A-to-I Human chr12 + 51050254 51050254 51050254 TTTATTATGAATTTTTTTTTTTTTTGAGTCTCACCGTGTCGCCCAGGCTGGAGTGCAATGGCATG TTTATTATGAATTTTTTTTTTTTTTGAGTCTCGCCGTGTCGCCCAGGCTGGAGTGCAATGGCATG A G LETMD1 Ensembl:ENSG00000050426 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1177644476 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2342317,Human_RBP_ID_11968343 RMVar_hsa_circ_3549,RMVar_hsa_circ_332234,RMVar_hsa_circ_24451,RMVar_hsa_circ_276574,RMVar_hsa_circ_280689,RMVar_hsa_circ_99391,RMVar_hsa_circ_156557,RMVar_hsa_circ_156558,RMVar_hsa_circ_156556 33748 RMVar_ID_33748 Human_SNP_ID_501000380 A-to-I Human chr12 + 51050278 51050278 51050278 TGAGTCTCACCGTGTCGCCCAGGCTGGAGTGCAATGGCATGATCTCGGTTCACTGCAACCTCTGC TGAGTCTCACCGTGTCGCCCAGGCTGGAGTGCGATGGCATGATCTCGGTTCACTGCAACCTCTGC A G LETMD1 Ensembl:ENSG00000050426 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs371775844 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3549,RMVar_hsa_circ_332234,RMVar_hsa_circ_24451,RMVar_hsa_circ_276574,RMVar_hsa_circ_280689,RMVar_hsa_circ_99391,RMVar_hsa_circ_156557,RMVar_hsa_circ_156558,RMVar_hsa_circ_156556 33749 RMVar_ID_33749 Human_SNP_ID_501000522 A-to-I Human chr12 + 51050830 51050830 51050830 GAGGTCGGGCGTTTGAGACCAGCCTGACCAACATAGAGAAGCACCGTCTCTACTAAAAATACAAA GAGGTCGGGCGTTTGAGACCAGCCTGACCAACGTAGAGAAGCACCGTCTCTACTAAAAATACAAA A G LETMD1 Ensembl:ENSG00000050426 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs943010550 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3549,RMVar_hsa_circ_332234,RMVar_hsa_circ_24451,RMVar_hsa_circ_276574,RMVar_hsa_circ_280689,RMVar_hsa_circ_99391,RMVar_hsa_circ_156557,RMVar_hsa_circ_156558,RMVar_hsa_circ_156556 33750 RMVar_ID_33750 Human_SNP_ID_501002185 A-to-I Human chr12 + 51057163 51057163 51057163 GGGAGGCTGAGACATGAGAATTGCTTGAACCCAGGAGGTGGATTGCAGTGAGCCAAGATCGCACC GGGAGGCTGAGACATGAGAATTGCTTGAACCCGGGAGGTGGATTGCAGTGAGCCAAGATCGCACC A G LETMD1 Ensembl:ENSG00000050426 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1173306189 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6194323,Human_RBP_ID_11968480,Human_RBP_ID_17561127 RMVar_hsa_circ_3549,RMVar_hsa_circ_24435,RMVar_hsa_circ_32378,RMVar_hsa_circ_280689,RMVar_hsa_circ_156558,RMVar_hsa_circ_58978,RMVar_hsa_circ_328605,RMVar_hsa_circ_338579 33751 RMVar_ID_33751 Human_SNP_ID_501012275 A-to-I Human chr12 - 51097103 51097103 51097103 ACAAAATTAGCCGGGTGTGGTGGCACGTGCCTATAATCCCACCTACTCAGGAGGCTGAGGCAGGA ACAAAATTAGCCGGGTGTGGTGGCACGTGCCTGTAATCCCACCTACTCAGGAGGCTGAGGCAGGA T C TFCP2 Ensembl:ENSG00000135457 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs543074552 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_156572,RMVar_hsa_circ_268989,RMVar_hsa_circ_156571,RMVar_hsa_circ_374238,RMVar_hsa_circ_267932 33752 RMVar_ID_33752 Human_SNP_ID_501012434 A-to-I Human chr12 - 51097782 51097782 51097782 GAACTCCTGGCCTCAAGTGATCAACCCGCCTCAGCCTCCCGAAGTGCTGGGATTACAGATGTGAA GAACTCCTGGCCTCAAGTGATCAACCCGCCTCGGCCTCCCGAAGTGCTGGGATTACAGATGTGAA T C TFCP2 Ensembl:ENSG00000135457 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs971454884 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_156572,RMVar_hsa_circ_268989,RMVar_hsa_circ_156571,RMVar_hsa_circ_374238,RMVar_hsa_circ_267932 33753 RMVar_ID_33753 Human_SNP_ID_501015408 A-to-I Human chr12 - 51110447 51110447 51110447 CTCTTGCCTCAGCCTCACCAGTAGCTGGGACTAGAGGCGCATGTCACCATGCCTGGCTAATTTTT CTCTTGCCTCAGCCTCACCAGTAGCTGGGACTGGAGGCGCATGTCACCATGCCTGGCTAATTTTT T C TFCP2 Ensembl:ENSG00000135457 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1244526316 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_156572,RMVar_hsa_circ_156571,RMVar_hsa_circ_374238,RMVar_hsa_circ_19291,RMVar_hsa_circ_372631,RMVar_hsa_circ_322067,RMVar_hsa_circ_345101,RMVar_hsa_circ_156579,RMVar_hsa_circ_331673,RMVar_hsa_circ_156575,RMVar_hsa_circ_343948,RMVar_hsa_circ_295495,RMVar_hsa_circ_278852,RMVar_hsa_circ_156582,RMVar_hsa_circ_156581,RMVar_hsa_circ_275608,RMVar_hsa_circ_277671,RMVar_hsa_circ_156583,RMVar_hsa_circ_294231,RMVar_hsa_circ_336952,RMVar_hsa_circ_347456,RMVar_hsa_circ_356620,RMVar_hsa_circ_345516,RMVar_hsa_circ_367409,RMVar_hsa_circ_156584,RMVar_hsa_circ_44400 33754 RMVar_ID_33754 Human_SNP_ID_501015646 A-to-I Human chr12 - 51111349 51111349 51111349 CTGAGGTCAGGAGTTTGAGAGCAGCATGGCCAACATGGTGAAACCCCATCTCTACTAAAGATACA CTGAGGTCAGGAGTTTGAGAGCAGCATGGCCAGCATGGTGAAACCCCATCTCTACTAAAGATACA T C TFCP2 Ensembl:ENSG00000135457 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs968451346 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_156572,RMVar_hsa_circ_156571,RMVar_hsa_circ_374238,RMVar_hsa_circ_19291,RMVar_hsa_circ_372631,RMVar_hsa_circ_322067,RMVar_hsa_circ_345101,RMVar_hsa_circ_156579,RMVar_hsa_circ_331673,RMVar_hsa_circ_156575,RMVar_hsa_circ_343948,RMVar_hsa_circ_295495,RMVar_hsa_circ_278852,RMVar_hsa_circ_280402,RMVar_hsa_circ_156582,RMVar_hsa_circ_156581,RMVar_hsa_circ_275608,RMVar_hsa_circ_277671,RMVar_hsa_circ_156583,RMVar_hsa_circ_294231,RMVar_hsa_circ_336952,RMVar_hsa_circ_356620,RMVar_hsa_circ_345516,RMVar_hsa_circ_367409,RMVar_hsa_circ_156584,RMVar_hsa_circ_292153,RMVar_hsa_circ_332507,RMVar_hsa_circ_156585 33755 RMVar_ID_33755 Human_SNP_ID_501015654 A-to-I Human chr12 - 51111419 51111412 51111419 GGTGTGGGCTGGGCACAGTGGCTCAAGCCTGTAATCCCAGCACTTTAGGAGGCCAAGGTGGGTGG GGTGTGGGCTGGGCACAGTGGCTCAAGCCTGT_______GCACTTTAGGAGGCCAAGGTGGGTGG CTGGGATT C TFCP2 Ensembl:ENSG00000135457 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1441239041 Functional Loss DEL dbSNP153 33..39 33 - - - RMVar_hsa_circ_156572,RMVar_hsa_circ_156571,RMVar_hsa_circ_374238,RMVar_hsa_circ_19291,RMVar_hsa_circ_372631,RMVar_hsa_circ_322067,RMVar_hsa_circ_345101,RMVar_hsa_circ_156579,RMVar_hsa_circ_331673,RMVar_hsa_circ_156575,RMVar_hsa_circ_343948,RMVar_hsa_circ_295495,RMVar_hsa_circ_278852,RMVar_hsa_circ_280402,RMVar_hsa_circ_156582,RMVar_hsa_circ_156581,RMVar_hsa_circ_275608,RMVar_hsa_circ_277671,RMVar_hsa_circ_156583,RMVar_hsa_circ_294231,RMVar_hsa_circ_336952,RMVar_hsa_circ_356620,RMVar_hsa_circ_345516,RMVar_hsa_circ_367409,RMVar_hsa_circ_156584,RMVar_hsa_circ_292153,RMVar_hsa_circ_332507,RMVar_hsa_circ_156585 33756 RMVar_ID_33756 Human_SNP_ID_501016369 A-to-I Human chr12 - 51114896 51114896 51114896 CACCACACCTAGCTAATTTTTGTATTTTTGGTAGAGACGGGGTTTCACCATGTTGGCCAGGGTAG CACCACACCTAGCTAATTTTTGTATTTTTGGTGGAGACGGGGTTTCACCATGTTGGCCAGGGTAG T C TFCP2 Ensembl:ENSG00000135457 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1374041427 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_156572,RMVar_hsa_circ_156571,RMVar_hsa_circ_374238,RMVar_hsa_circ_19291,RMVar_hsa_circ_372631,RMVar_hsa_circ_322067,RMVar_hsa_circ_345101,RMVar_hsa_circ_156579,RMVar_hsa_circ_331673,RMVar_hsa_circ_156575,RMVar_hsa_circ_343948,RMVar_hsa_circ_295495,RMVar_hsa_circ_278852,RMVar_hsa_circ_280402,RMVar_hsa_circ_156582,RMVar_hsa_circ_156581,RMVar_hsa_circ_275608,RMVar_hsa_circ_277671,RMVar_hsa_circ_156583,RMVar_hsa_circ_294231,RMVar_hsa_circ_336952,RMVar_hsa_circ_356620,RMVar_hsa_circ_345516,RMVar_hsa_circ_367409,RMVar_hsa_circ_156584,RMVar_hsa_circ_292153,RMVar_hsa_circ_332507,RMVar_hsa_circ_156585 33757 RMVar_ID_33757 Human_SNP_ID_501016384 A-to-I Human chr12 - 51114985 51114985 51114985 GCGATATCAACTCACCACAACCTCTCCCTCCCAGGTTCAAGTGATTCTCCTGCCTCAGCCTCCAA GCGATATCAACTCACCACAACCTCTCCCTCCCGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCAA T C TFCP2 Ensembl:ENSG00000135457 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1259828818 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_156572,RMVar_hsa_circ_156571,RMVar_hsa_circ_374238,RMVar_hsa_circ_19291,RMVar_hsa_circ_372631,RMVar_hsa_circ_322067,RMVar_hsa_circ_345101,RMVar_hsa_circ_156579,RMVar_hsa_circ_331673,RMVar_hsa_circ_156575,RMVar_hsa_circ_343948,RMVar_hsa_circ_295495,RMVar_hsa_circ_278852,RMVar_hsa_circ_280402,RMVar_hsa_circ_156582,RMVar_hsa_circ_156581,RMVar_hsa_circ_275608,RMVar_hsa_circ_277671,RMVar_hsa_circ_156583,RMVar_hsa_circ_294231,RMVar_hsa_circ_336952,RMVar_hsa_circ_356620,RMVar_hsa_circ_345516,RMVar_hsa_circ_367409,RMVar_hsa_circ_156584,RMVar_hsa_circ_292153,RMVar_hsa_circ_332507,RMVar_hsa_circ_156585 33758 RMVar_ID_33758 Human_SNP_ID_501021042 A-to-I Human chr12 - 51133383 51133383 51133383 GGAGGATGGCTTGAGCCCAAGAGGCTGAGGCTACAGTGAGTGGTGATTACGCCACTGTACCCCAC GGAGGATGGCTTGAGCCCAAGAGGCTGAGGCTGCAGTGAGTGGTGATTACGCCACTGTACCCCAC T C TFCP2 Ensembl:ENSG00000135457 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs575527807 Functional Loss SNV dbSNP153 33..33 33 - - - 33759 RMVar_ID_33759 Human_SNP_ID_501021843 A-to-I Human chr12 - 51136770 51136770 51136770 CATGCCGGCTAATTATTTTTTATACTTTTAGTAGAGATGGGGTTTTACCATGTCAGCTAGACTAG CATGCCGGCTAATTATTTTTTATACTTTTAGTGGAGATGGGGTTTTACCATGTCAGCTAGACTAG T C TFCP2 Ensembl:ENSG00000135457 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1295960251 Functional Loss SNV dbSNP153 33..33 33 - - - 33760 RMVar_ID_33760 Human_SNP_ID_501022601 A-to-I Human chr12 - 51140376 51140376 51140376 AAAAAGGAAGAAAGACAGAGTCTCACTATATTACTCAGGCTGGTGTTGAATTACTGGGCTCAAGT AAAAAGGAAGAAAGACAGAGTCTCACTATATTGCTCAGGCTGGTGTTGAATTACTGGGCTCAAGT T C TFCP2 Ensembl:ENSG00000135457 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs955588855 Functional Loss SNV dbSNP153 33..33 33 - - - 33761 RMVar_ID_33761 Human_SNP_ID_501022605 A-to-I Human chr12 - 51140392 51140389 51140393 AAAGAAGGAAGGAAGAAAAAAGGAAGAAAGACAGAGTCTCACTATATTACTCAGGCTGGTGTTGA AAAGAAGGAAGGAAGAAAAAAGGAAGAAAGA____GTCTCACTATATTACTCAGGCTGGTGTTGA CTCTG C TFCP2 Ensembl:ENSG00000135457 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs979312435 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_24977819 33762 RMVar_ID_33762 Human_SNP_ID_501026134 A-to-I Human chr12 - 51154680 51154680 51154680 ACATTTATTTATTTATTTAGAGATGGACTCTCACTGTGTCACCTAGGCTGGAGTGCAGTGGCACC ACATTTATTTATTTATTTAGAGATGGACTCTCGCTGTGTCACCTAGGCTGGAGTGCAGTGGCACC T C TFCP2 Ensembl:ENSG00000135457 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs780459107 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11969892 33763 RMVar_ID_33763 Human_SNP_ID_501026739 A-to-I Human chr12 - 51157154 51157154 51157154 AAAATTAGCCGGCCGTAGTGGCACATGCCTGTAATCCTAGCTACTTAGGAGGCTGAGGCAGGAGA AAAATTAGCCGGCCGTAGTGGCACATGCCTGTCATCCTAGCTACTTAGGAGGCTGAGGCAGGAGA T G TFCP2 Ensembl:ENSG00000135457 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1242953323 Functional Loss SNV dbSNP153 33..33 33 - - - 33764 RMVar_ID_33764 Human_SNP_ID_501027023 A-to-I Human chr12 - 51158034 51158034 51158034 TTGTGCCACATCACTCCAGCCTTGGTGACAGAACAAGACTCTGTTTCTAAAAAAAAATTAAGATT TTGTGCCACATCACTCCAGCCTTGGTGACAGAGCAAGACTCTGTTTCTAAAAAAAAATTAAGATT T C TFCP2 Ensembl:ENSG00000135457 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs931760745 Functional Loss SNV dbSNP153 33..33 33 - - - 33765 RMVar_ID_33765 Human_SNP_ID_501027047 A-to-I Human chr12 - 51158147 51158147 51158147 AAAATTAGCTGGGCATGGTGATATATTCCTGTAGTCCTAGCTACTAGCTACTCAGGAGGCTGAGG AAAATTAGCTGGGCATGGTGATATATTCCTGTGGTCCTAGCTACTAGCTACTCAGGAGGCTGAGG T C TFCP2 Ensembl:ENSG00000135457 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1321910555 Functional Loss SNV dbSNP153 33..33 33 - - - 33766 RMVar_ID_33766 Human_SNP_ID_501027160 A-to-I Human chr12 - 51158653 51158653 51158653 GAGACCCTGTCTTTACTAAAAATATAAAAATTAGCTGGGCATGGTGGCTCATGCCTGTAGTCCCA GAGACCCTGTCTTTACTAAAAATATAAAAATTGGCTGGGCATGGTGGCTCATGCCTGTAGTCCCA T C TFCP2 Ensembl:ENSG00000135457 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1262716921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24977940 33767 RMVar_ID_33767 Human_SNP_ID_501027414 A-to-I Human chr12 - 51159476 51159476 51159476 AAATTAGCTGGGCATGGTGGTGGGCGCCTGTAATCCCAGCTACTTGGGCGGCTGAGGCATGAGAA AAATTAGCTGGGCATGGTGGTGGGCGCCTGTAGTCCCAGCTACTTGGGCGGCTGAGGCATGAGAA T C TFCP2 Ensembl:ENSG00000135457 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1018829714 Functional Loss SNV dbSNP153 33..33 33 - - - 33768 RMVar_ID_33768 Human_SNP_ID_501027426 A-to-I Human chr12 - 51159534 51159526 51159534 GTGGGTTCGAGACCAGCCTCGCCAATGTGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAG GTGGGTTCGAGACCAGCCTCGCCAATGTGGTG________TCTCTACTAAAAATACAAAAATTAG ACGGGGTTT A TFCP2 Ensembl:ENSG00000135457 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1374919244 Functional Loss DEL dbSNP153 33..40 33 - - - 33769 RMVar_ID_33769 Human_SNP_ID_501027483 A-to-I Human chr12 - 51159687 51159687 51159687 GCCTGGGAGTTTGAGGCCAGCCTGGGCAACATAGTGATACCCTGTCTCTAAAAACAAACCCAAAT GCCTGGGAGTTTGAGGCCAGCCTGGGCAACATGGTGATACCCTGTCTCTAAAAACAAACCCAAAT T C TFCP2 Ensembl:ENSG00000135457 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1367340489 Functional Loss SNV dbSNP153 33..33 33 - - - 33770 RMVar_ID_33770 Human_SNP_ID_501028583 A-to-I Human chr12 - 51164090 51164090 51164090 CAAGTGATCCTCCTACCTCAGCCTCCTGAGTAACTGAGACTACAGGCATGCATCACCAAACCCAG CAAGTGATCCTCCTACCTCAGCCTCCTGAGTAGCTGAGACTACAGGCATGCATCACCAAACCCAG T C TFCP2 Ensembl:ENSG00000135457 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1364461869 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3407974 33771 RMVar_ID_33771 Human_SNP_ID_501029476 A-to-I Human chr12 - 51167895 51167895 51167895 CACCACACCTGGCCAGTTTTTCTACTTTTTGTAGAGACTAGATCTTGCTGTGTTGCTCAGGCTGA CACCACACCTGGCCAGTTTTTCTACTTTTTGTGGAGACTAGATCTTGCTGTGTTGCTCAGGCTGA T C TFCP2 Ensembl:ENSG00000135457 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1412551355 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11970208 33772 RMVar_ID_33772 Human_SNP_ID_501029482 A-to-I Human chr12 - 51167939 51167939 51167939 TTCCTGCTGCAGCCTCCTGACTGGCTAGGACTACAGGGTCACACCACCACACCTGGCCAGTTTTT TTCCTGCTGCAGCCTCCTGACTGGCTAGGACTGCAGGGTCACACCACCACACCTGGCCAGTTTTT T C TFCP2 Ensembl:ENSG00000135457 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs908267037 Functional Loss SNV dbSNP153 33..33 33 - - - 33773 RMVar_ID_33773 Human_SNP_ID_501029488 A-to-I Human chr12 - 51167979 51167979 51167979 GTAGCTCATTGCAGCCTCAAACTCCTGGGCTCAAGTGATCTTCCTGCTGCAGCCTCCTGACTGGC GTAGCTCATTGCAGCCTCAAACTCCTGGGCTCGAGTGATCTTCCTGCTGCAGCCTCCTGACTGGC T C TFCP2 Ensembl:ENSG00000135457 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256888113 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8378252 33774 RMVar_ID_33774 Human_SNP_ID_501029910 A-to-I Human chr12 - 51169701 51169701 51169701 TCTTTTCTTTTTGAGACGGGTCCTGTTCTGTCACTCAGGCTGGGGTGCAGTGGCACCATCTCGGC TCTTTTCTTTTTGAGACGGGTCCTGTTCTGTCCCTCAGGCTGGGGTGCAGTGGCACCATCTCGGC T G TFCP2 Ensembl:ENSG00000135457 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs939727907 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11970251,Human_RBP_ID_19779531,Human_RBP_ID_23158058 33775 RMVar_ID_33775 Human_SNP_ID_501040585 A-to-I Human chr12 - 51212983 51212983 51212983 GCAGTAAGCCGAGATCCCGCCGCTGCACTCCAACCTGGGTGACAGAGCGAGACTCCGCCTCGAAA GCAGTAAGCCGAGATCCCGCCGCTGCACTCCAGCCTGGGTGACAGAGCGAGACTCCGCCTCGAAA T C POU6F1 Ensembl:ENSG00000184271 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs797022209 Functional Loss SNV dbSNP153 33..33 33 - - - 33776 RMVar_ID_33776 Human_SNP_ID_501040864 A-to-I Human chr12 - 51214103 51214103 51214103 GAGTCTCACTGTGTCTCCCAGACAGGAGTGCAATGGCATGATCTCGGCTCACTGCAACCTCCGCC GAGTCTCACTGTGTCTCCCAGACAGGAGTGCAGTGGCATGATCTCGGCTCACTGCAACCTCCGCC T C POU6F1 Ensembl:ENSG00000184271 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs867539664 Functional Loss SNV dbSNP153 33..33 33 - - - 33777 RMVar_ID_33777 Human_SNP_ID_501077160 A-to-I Human chr12 - 51353659 51353659 51353659 GTCCAGTGAAATGATATATTCTGGCTGGGCACAGTGGCTCACACCTGTAATCCTAGCACTTTGGG GTCCAGTGAAATGATATATTCTGGCTGGGCACGGTGGCTCACACCTGTAATCCTAGCACTTTGGG T C GALNT6 Ensembl:ENSG00000139629 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956142500 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17471874 Human_miRNA_ID_2890549 RMVar_hsa_circ_124821,RMVar_hsa_circ_156595 33778 RMVar_ID_33778 Human_SNP_ID_501078595 A-to-I Human chr12 - 51359244 51359243 51359244 GTTCCGGACCAAGAGCCCCCACACCTTCCCCAAGGGCACTAGTGTCATTGCTCGCAATCAAGTGC GTTCCGGACCAAGAGCCCCCACACCTTCCCCA_GGGCACTAGTGTCATTGCTCGCAATCAAGTGC CT C GALNT6 Ensembl:ENSG00000139629 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs748270490 Functional Loss DEL dbSNP153 33..33 33 - - - Human_Splice_Rec_1370130,Human_Splice_Rec_1370152,Human_Splice_Rec_1370176 RMVar_hsa_circ_98975,RMVar_hsa_circ_124821,RMVar_hsa_circ_156595,RMVar_hsa_circ_156596 33779 RMVar_ID_33779 Human_SNP_ID_501080227 A-to-I Human chr12 - 51366106 51366106 51366106 CGAGACCAGCCTGGCCAATATGGTGAAATGCTATCTCTACTAAAAATGTAAAAATGAGCCAGGCA CGAGACCAGCCTGGCCAATATGGTGAAATGCTGTCTCTACTAAAAATGTAAAAATGAGCCAGGCA T C GALNT6 Ensembl:ENSG00000139629 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928456762 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124821,RMVar_hsa_circ_156595 33780 RMVar_ID_33780 Human_SNP_ID_501080809 A-to-I Human chr12 - 51368633 51368633 51368633 GGGAGGCCGAGGCGGGCAGATCACTTGAGGTCAGGAATTCGAGACCAGCCTGGCCAACATGGTGA GGGAGGCCGAGGCGGGCAGATCACTTGAGGTCGGGAATTCGAGACCAGCCTGGCCAACATGGTGA T C GALNT6 Ensembl:ENSG00000139629 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1434150543 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124821,RMVar_hsa_circ_156595 33781 RMVar_ID_33781 Human_SNP_ID_501082598 A-to-I Human chr12 - 51376413 51376413 51376413 GTCAGGTTGGTCTCGAACTCCCGAACTCAGGTAATCTGCCTGCTCCAGCCTCCCAAAGTGCTGGG GTCAGGTTGGTCTCGAACTCCCGAACTCAGGTGATCTGCCTGCTCCAGCCTCCCAAAGTGCTGGG T C GALNT6 Ensembl:ENSG00000139629 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1305105300 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124821,RMVar_hsa_circ_156595 33782 RMVar_ID_33782 Human_SNP_ID_501084750 A-to-I Human chr12 - 51384462 51384462 51384462 GTCTTGAACTCCTGGCCTAAAGTGATCTGCCCACCATGGCCTCCCAAAGTGCTGGGATTTCAGGT GTCTTGAACTCCTGGCCTAAAGTGATCTGCCCTCCATGGCCTCCCAAAGTGCTGGGATTTCAGGT T A GALNT6 Ensembl:ENSG00000139629 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1225368188 Functional Loss SNV dbSNP153 33..33 33 - - - 33783 RMVar_ID_33783 Human_SNP_ID_501099660 A-to-I Human chr12 + 51449291 51449291 51449291 AGGACTTGTCTCTACTAAAAATCAAAAAAATTAGCTGGGCGTGGTGGTACACGCCTGTGGTCCCA AGGACTTGTCTCTACTAAAAATCAAAAAAATTGGCTGGGCGTGGTGGTACACGCCTGTGGTCCCA A G SLC4A8 Ensembl:ENSG00000050438 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs888171094 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1662,RMVar_hsa_circ_18841,RMVar_hsa_circ_40184,RMVar_hsa_circ_325448,RMVar_hsa_circ_355427,RMVar_hsa_circ_274920,RMVar_hsa_circ_34333,RMVar_hsa_circ_14178,RMVar_hsa_circ_16448,RMVar_hsa_circ_1822,RMVar_hsa_circ_156598,RMVar_hsa_circ_156599 33784 RMVar_ID_33784 Human_SNP_ID_501113898 A-to-I Human chr12 + 51511586 51511586 51511586 TAATTTTTGTATTTTAGTAGAGACGAAGTTTCACTATGTTGGCCAGGCTGGTCTGAAACTCCTGG TAATTTTTGTATTTTAGTAGAGACGAAGTTTCCCTATGTTGGCCAGGCTGGTCTGAAACTCCTGG A C SLC4A8 Ensembl:ENSG00000050438 Protein coding 3'UTR GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs964524882 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265102 33785 RMVar_ID_33785 Human_SNP_ID_501114317 A-to-I Human chr12 + 51513594 51513594 51513594 CTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTATAGGCGCGCACCACCATGCCCAGCTAATTTTT CTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTGTAGGCGCGCACCACCATGCCCAGCTAATTTTT A G SLC4A8 Ensembl:ENSG00000050438 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1014456592 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265102 33786 RMVar_ID_33786 Human_SNP_ID_501136610 A-to-I Human chr12 + 51612925 51612925 51612925 TTGTATTTTTAGTAGAGATGGGGTTTCACCATATTGGCCAGACTGGTCTTGAACTCCTGACATCC TTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGACTGGTCTTGAACTCCTGACATCC A G SCN8A Ensembl:ENSG00000196876 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1436430161 Functional Loss SNV dbSNP153 33..33 33 - - - 33787 RMVar_ID_33787 Human_SNP_ID_501148805 A-to-I Human chr12 + 51667424 51667424 51667424 GAGTCTAACTCCAAGTTGGAGTGCAGTGATGCAATCATAGGTCACTGCAGCCTCAACCTCCTGGG GAGTCTAACTCCAAGTTGGAGTGCAGTGATGCCATCATAGGTCACTGCAGCCTCAACCTCCTGGG A C SCN8A Ensembl:ENSG00000196876 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1233138354 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 33788 RMVar_ID_33788 Human_SNP_ID_501177251 A-to-I Human chr12 + 51793883 51793883 51793883 AACAGAAAGAAAGGCCAGGCATGATGGCTCACACCTGTAATCCTAGCATTTTGGGAGGCCAAGGA AACAGAAAGAAAGGCCAGGCATGATGGCTCACTCCTGTAATCCTAGCATTTTGGGAGGCCAAGGA A T SCN8A Ensembl:ENSG00000196876 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1310272554 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_329115,RMVar_hsa_circ_156619,RMVar_hsa_circ_96299,RMVar_hsa_circ_156627,RMVar_hsa_circ_341453,RMVar_hsa_circ_32886,RMVar_hsa_circ_156633,RMVar_hsa_circ_54131,RMVar_hsa_circ_337703,RMVar_hsa_circ_156636,RMVar_hsa_circ_156637,RMVar_hsa_circ_370858 33789 RMVar_ID_33789 Human_SNP_ID_501177252 A-to-I Human chr12 + 51793889 51793889 51793889 AAGAAAGGCCAGGCATGATGGCTCACACCTGTAATCCTAGCATTTTGGGAGGCCAAGGAAGACAG AAGAAAGGCCAGGCATGATGGCTCACACCTGTGATCCTAGCATTTTGGGAGGCCAAGGAAGACAG A G SCN8A Ensembl:ENSG00000196876 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs533109471 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_329115,RMVar_hsa_circ_156619,RMVar_hsa_circ_96299,RMVar_hsa_circ_156627,RMVar_hsa_circ_341453,RMVar_hsa_circ_32886,RMVar_hsa_circ_156633,RMVar_hsa_circ_54131,RMVar_hsa_circ_337703,RMVar_hsa_circ_156636,RMVar_hsa_circ_156637,RMVar_hsa_circ_370858 33790 RMVar_ID_33790 Human_SNP_ID_501424008 A-to-I Human chr12 + 52731763 52731763 52731763 GACAACAGCCTTCCTCATCCCACTGCTAGTCTAGATCACCACACTTCCCAAAATTGACAGGATCG GACAACAGCCTTCCTCATCCCACTGCTAGTCTGGATCACCACACTTCCCAAAATTGACAGGATCG A G AC055716.2 Ensembl:ENSG00000257616 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1231676479 Functional Loss SNV dbSNP153 33..33 33 - - - 33791 RMVar_ID_33791 Human_SNP_ID_501471560 A-to-I Human chr12 - 52902855 52902855 52902855 AGTGCGTGCCACCATGCCCGGTTAATTTTTGTATTATTTGTAGGGACAGGGTTTCAATATGTTGG AGTGCGTGCCACCATGCCCGGTTAATTTTTGTGTTATTTGTAGGGACAGGGTTTCAATATGTTGG T C KRT8 Ensembl:ENSG00000170421 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1447206610 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98349,RMVar_hsa_circ_114394,RMVar_hsa_circ_124383,RMVar_hsa_circ_105831,RMVar_hsa_circ_156770,RMVar_hsa_circ_156772,RMVar_hsa_circ_156771,RMVar_hsa_circ_156769,RMVar_hsa_circ_109596,RMVar_hsa_circ_156783 33792 RMVar_ID_33792 Human_SNP_ID_501500740 A-to-I Human chr12 + 53010674 53010674 53010674 TTTTGTTTGTTTTTGTTTTTGTTTTGAGACAGAGTCTCACTATGGCTCAGGCTGGAGTGCAGTGG TTTTGTTTGTTTTTGTTTTTGTTTTGAGACAGTGTCTCACTATGGCTCAGGCTGGAGTGCAGTGG A T EIF4B Ensembl:ENSG00000063046 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs984247138 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6195674,Human_RBP_ID_11972127 RMVar_hsa_circ_40334,RMVar_hsa_circ_76754,RMVar_hsa_circ_156797 33793 RMVar_ID_33793 Human_SNP_ID_501501720 A-to-I Human chr12 + 53014301 53014301 53014301 TGGCGTGGTGGCACGCGCCTGTAGTCCCAGCCACTTGGGAGGCTGAGGCAGGAGAAATTGCTTGA TGGCGTGGTGGCACGCGCCTGTAGTCCCAGCCTCTTGGGAGGCTGAGGCAGGAGAAATTGCTTGA A T EIF4B Ensembl:ENSG00000063046 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1310701644 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40334,RMVar_hsa_circ_76754,RMVar_hsa_circ_156797 33794 RMVar_ID_33794 Human_SNP_ID_501502647 A-to-I Human chr12 + 53017843 53017843 53017843 TTGAACTCCTGACCTCATGACCCACCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAG TTGAACTCCTGACCTCATGACCCACCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAG A G EIF4B Ensembl:ENSG00000063046 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1440494377 Functional Loss SNV dbSNP153 33..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 33795 RMVar_ID_33795 Human_SNP_ID_501502714 A-to-I Human chr12 + 53018130 53018130 53018130 GTCCTGTCTCAGCCTCCCAAGTAGATGGGATTACTGGCACATGCCACCACACCTGGCTAATTTTT GTCCTGTCTCAGCCTCCCAAGTAGATGGGATTGCTGGCACATGCCACCACACCTGGCTAATTTTT A G EIF4B Ensembl:ENSG00000063046 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1169069745 Functional Loss SNV dbSNP153 33..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 33796 RMVar_ID_33796 Human_SNP_ID_501502729 A-to-I Human chr12 + 53018174 53018174 53018174 CACCACACCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATAATGGTCAGGCTGG CACCACACCTGGCTAATTTTTGTATTTTTAGTGGAGACAGGGTTTCACCATAATGGTCAGGCTGG A G EIF4B Ensembl:ENSG00000063046 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs565408006 Functional Loss SNV dbSNP153 33..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 33797 RMVar_ID_33797 Human_SNP_ID_501503228 A-to-I Human chr12 + 53019546 53019544 53019547 TGGATTACATGCCCAGCTAATTTTTTGTATTTAGTAGAGATAGGGTTGCACTATGTTGGTCAGGC TGGATTACATGCCCAGCTAATTTTTTGTATT___TAGAGATAGGGTTGCACTATGTTGGTCAGGC TTAG T EIF4B Ensembl:ENSG00000063046 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1319449121 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_11972408 RMVar_hsa_circ_76754,RMVar_hsa_circ_156797,RMVar_hsa_circ_82258,RMVar_hsa_circ_86249,RMVar_hsa_circ_123410,RMVar_hsa_circ_294205,RMVar_hsa_circ_304371,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_156805,RMVar_hsa_circ_156804,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_313304,RMVar_hsa_circ_101989,RMVar_hsa_circ_284764,RMVar_hsa_circ_91253,RMVar_hsa_circ_156808,RMVar_hsa_circ_156812,RMVar_hsa_circ_156814,RMVar_hsa_circ_76890,RMVar_hsa_circ_156813,RMVar_hsa_circ_156810,RMVar_hsa_circ_156811,RMVar_hsa_circ_156809 33798 RMVar_ID_33798 Human_SNP_ID_501504087 A-to-I Human chr12 + 53022948 53022948 53022948 CGCTTTGGGAGGTCAAGGCAGGTGGATTGCTTAAGGCCAGGAGTTTGAGAGCAGCCTGGGCGACA CGCTTTGGGAGGTCAAGGCAGGTGGATTGCTTCAGGCCAGGAGTTTGAGAGCAGCCTGGGCGACA A C EIF4B Ensembl:ENSG00000063046 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1170189111 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76754,RMVar_hsa_circ_156797,RMVar_hsa_circ_15097,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_156820,RMVar_hsa_circ_156822,RMVar_hsa_circ_156821,RMVar_hsa_circ_156819,RMVar_hsa_circ_156825,RMVar_hsa_circ_89981 33799 RMVar_ID_33799 Human_SNP_ID_501504586 A-to-I Human chr12 + 53024748 53024748 53024748 GCAATCTTGGCTCACTGCAACCTCTGCCTGCCAGGTTCAGGGTGTTCCTCATGCCTCAGCCTCCT GCAATCTTGGCTCACTGCAACCTCTGCCTGCCGGGTTCAGGGTGTTCCTCATGCCTCAGCCTCCT A G EIF4B Ensembl:ENSG00000063046 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1294279680 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11972560 RMVar_hsa_circ_76754,RMVar_hsa_circ_156797,RMVar_hsa_circ_15097,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_156820,RMVar_hsa_circ_156822,RMVar_hsa_circ_156821,RMVar_hsa_circ_156819,RMVar_hsa_circ_156825,RMVar_hsa_circ_89981 33800 RMVar_ID_33800 Human_SNP_ID_501505768 A-to-I Human chr12 + 53029003 53029003 53029003 CAAAAATTAGGTGGCCGTAGTGGCACATACCTATCATCCCAGCTACTCGGGTGGCTGAGGCAGGA CAAAAATTAGGTGGCCGTAGTGGCACATACCTGTCATCCCAGCTACTCGGGTGGCTGAGGCAGGA A G EIF4B Ensembl:ENSG00000063046 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1039899099 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11972759 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_82628,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_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_110979,RMVar_hsa_circ_86627,RMVar_hsa_circ_156835,RMVar_hsa_circ_156836,RMVar_hsa_circ_156837 33801 RMVar_ID_33801 Human_SNP_ID_501505769 A-to-I Human chr12 + 53029003 53029003 53029003 CAAAAATTAGGTGGCCGTAGTGGCACATACCTATCATCCCAGCTACTCGGGTGGCTGAGGCAGGA CAAAAATTAGGTGGCCGTAGTGGCACATACCTTTCATCCCAGCTACTCGGGTGGCTGAGGCAGGA A T EIF4B Ensembl:ENSG00000063046 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1039899099 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11972759 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_82628,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_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_110979,RMVar_hsa_circ_86627,RMVar_hsa_circ_156835,RMVar_hsa_circ_156836,RMVar_hsa_circ_156837 33802 RMVar_ID_33802 Human_SNP_ID_501505772 A-to-I Human chr12 + 53029015 53029015 53029015 GGCCGTAGTGGCACATACCTATCATCCCAGCTACTCGGGTGGCTGAGGCAGGAGAATTGCTTGAG GGCCGTAGTGGCACATACCTATCATCCCAGCTGCTCGGGTGGCTGAGGCAGGAGAATTGCTTGAG A G EIF4B Ensembl:ENSG00000063046 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs533476157 Functional Loss SNV dbSNP153 33..33 33 - - - 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_82628,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_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_110979,RMVar_hsa_circ_86627,RMVar_hsa_circ_156835,RMVar_hsa_circ_156836,RMVar_hsa_circ_156837 33803 RMVar_ID_33803 Human_SNP_ID_501505942 A-to-I Human chr12 + 53029515 53029515 53029515 CTCTTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGTGCACGCCACCATGCCCAGCTAATTTTT CTCTTGCCTCAGCCTCCCGAGTAGCTGGGACTGCAGGTGCACGCCACCATGCCCAGCTAATTTTT A G EIF4B Ensembl:ENSG00000063046 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1319124060 Functional Loss SNV dbSNP153 33..33 33 - - - 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_82628,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_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_110979,RMVar_hsa_circ_86627,RMVar_hsa_circ_156835,RMVar_hsa_circ_156836,RMVar_hsa_circ_156837 33804 RMVar_ID_33804 Human_SNP_ID_501505976 A-to-I Human chr12 + 53029654 53029654 53029654 CCTTGGCCTCCCAAAGTGTTGGGATTACAGGCATGAGCCACCGTGCCCGGCCAAATTTTTCCTAT CCTTGGCCTCCCAAAGTGTTGGGATTACAGGCGTGAGCCACCGTGCCCGGCCAAATTTTTCCTAT A G EIF4B Ensembl:ENSG00000063046 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7967789 Functional Loss SNV dbSNP153 33..33 33 - - - 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_82628,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_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_110979,RMVar_hsa_circ_86627,RMVar_hsa_circ_156835,RMVar_hsa_circ_156836,RMVar_hsa_circ_156837 33805 RMVar_ID_33805 Human_SNP_ID_501506547 A-to-I Human chr12 + 53031478 53031478 53031478 TGATATTTTTTCTAAAGATGGGGTTTCTCCACATTGCCCAGGCTGGTTTTAAACTTCCAAGTTCA TGATATTTTTTCTAAAGATGGGGTTTCTCCACGTTGCCCAGGCTGGTTTTAAACTTCCAAGTTCA A G EIF4B Ensembl:ENSG00000063046 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1359408632 Functional Loss SNV dbSNP153 33..33 33 - - - 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_82628,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_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_110979,RMVar_hsa_circ_86627,RMVar_hsa_circ_156835,RMVar_hsa_circ_156836,RMVar_hsa_circ_156837 33806 RMVar_ID_33806 Human_SNP_ID_501545657 A-to-I Human chr12 - 53174115 53174115 53174115 TATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGGTCTCGATCTCCTGACCTCGTGA TATTTTTAGTAGAGACGGGGTTTCACCGTGTTCGCCAGGATGGTCTCGATCTCCTGACCTCGTGA T G CSAD Ensembl:ENSG00000139631 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1350051879 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_116310 33807 RMVar_ID_33807 Human_SNP_ID_501545794 A-to-I Human chr12 - 53174550 53174550 53174550 ACCTCAGGTGATCCACCCACCTCAGCATCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCACAC ACCTCAGGTGATCCACCCACCTCAGCATCCCAGAGTGCTGGGATTACAGGTGTGAGCCACCACAC T C CSAD Ensembl:ENSG00000139631 Protein coding intron GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 ASD brains,Fragile X samples from UC Davis FXTAS brain repository;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 30559470,31158229,31158229,31158229 RNA-Seq:(High) rs1490183084 Functional Loss SNV dbSNP153 33..33 33 - - - 33808 RMVar_ID_33808 Human_SNP_ID_501545804 A-to-I Human chr12 - 53174628 53174628 53174628 CACCACGCCCGGCTAATTGTGTATTTTTTAGTAGAAATGAGGTTTCGCCATGTTGGCCAGGCTGG CACCACGCCCGGCTAATTGTGTATTTTTTAGTGGAAATGAGGTTTCGCCATGTTGGCCAGGCTGG T C CSAD Ensembl:ENSG00000139631 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1283440142 Functional Loss SNV dbSNP153 33..33 33 - - - 33809 RMVar_ID_33809 Human_SNP_ID_501545846 A-to-I Human chr12 - 53174778 53174778 53174778 CATATATATATATATTTTTGAAATGGAGTCCCACTCTGTCGCCCAGGCTGGAGTGCAGTGGTACC CATATATATATATATTTTTGAAATGGAGTCCCCCTCTGTCGCCCAGGCTGGAGTGCAGTGGTACC T G CSAD Ensembl:ENSG00000139631 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs1022696458 Functional Loss SNV dbSNP153 33..33 33 - - - 33810 RMVar_ID_33810 Human_SNP_ID_501546217 A-to-I Human chr12 - 53176298 53176298 53176298 TCAAGCGATTCTTCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCATGCACCACCACACCCG TCAAGCGATTCTTCTGCCTCAGCCTCCCAAGTCGCTGGGATTACAGGCATGCACCACCACACCCG T G CSAD Ensembl:ENSG00000139631 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1254963244 Functional Loss SNV dbSNP153 33..33 33 - - - 33811 RMVar_ID_33811 Human_SNP_ID_501546218 A-to-I Human chr12 - 53176302 53176302 53176302 GGGTTCAAGCGATTCTTCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCATGCACCACCACA GGGTTCAAGCGATTCTTCTGCCTCAGCCTCCCCAGTAGCTGGGATTACAGGCATGCACCACCACA T G CSAD Ensembl:ENSG00000139631 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1447957970 Functional Loss SNV dbSNP153 33..33 33 - - - 33812 RMVar_ID_33812 Human_SNP_ID_501546222 A-to-I Human chr12 - 53176310 53176310 53176310 TGCCTCCCGGGTTCAAGCGATTCTTCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCATGCA TGCCTCCCGGGTTCAAGCGATTCTTCTGCCTCCGCCTCCCAAGTAGCTGGGATTACAGGCATGCA T G CSAD Ensembl:ENSG00000139631 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1168137039 Functional Loss SNV dbSNP153 33..33 33 - - - 33813 RMVar_ID_33813 Human_SNP_ID_501546236 A-to-I Human chr12 - 53176371 53176371 53176371 AATTTTGCTCTTGCTGCCCAGGCTGGAATGCAATGGTGCGATCTTGGCTCACTGCAACCTCTGCC AATTTTGCTCTTGCTGCCCAGGCTGGAATGCAGTGGTGCGATCTTGGCTCACTGCAACCTCTGCC T C CSAD Ensembl:ENSG00000139631 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1350524202 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11973426 33814 RMVar_ID_33814 Human_SNP_ID_501546259 A-to-I Human chr12 - 53176475 53176475 53176475 GACCTCGTGATCCACCCGCCCTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCTCC GACCTCGTGATCCACCCGCCCTGGCCTCCCAACGTGCTGGGATTACAGGCGTGAGCCACTGCTCC T G CSAD Ensembl:ENSG00000139631 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1326257382 Functional Loss SNV dbSNP153 33..33 33 - - - 33815 RMVar_ID_33815 Human_SNP_ID_501546283 A-to-I Human chr12 - 53176571 53176571 53176571 GGGACTGCAGGTGCCCACCACCATGCCGGGCTAATTTTTTGTATTTTTAGTAGAGATGGGGTTTC GGGACTGCAGGTGCCCACCACCATGCCGGGCTGATTTTTTGTATTTTTAGTAGAGATGGGGTTTC T C CSAD Ensembl:ENSG00000139631 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1004858978 Functional Loss SNV dbSNP153 33..33 33 - - - 33816 RMVar_ID_33816 Human_SNP_ID_501546284 A-to-I Human chr12 - 53176571 53176571 53176571 GGGACTGCAGGTGCCCACCACCATGCCGGGCTAATTTTTTGTATTTTTAGTAGAGATGGGGTTTC GGGACTGCAGGTGCCCACCACCATGCCGGGCTCATTTTTTGTATTTTTAGTAGAGATGGGGTTTC T G CSAD Ensembl:ENSG00000139631 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1004858978 Functional Loss SNV dbSNP153 33..33 33 - - - 33817 RMVar_ID_33817 Human_SNP_ID_501546353 A-to-I Human chr12 - 53176881 53176881 53176881 AAAAAATTAAAAAATTAACCCGGCATGCTGGCATGTGCCTGTAGTCCTAGCTACTCAGGAGGCTG AAAAAATTAAAAAATTAACCCGGCATGCTGGCGTGTGCCTGTAGTCCTAGCTACTCAGGAGGCTG T C CSAD Ensembl:ENSG00000139631 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1488971203 Functional Loss SNV dbSNP153 33..33 33 - - - 33818 RMVar_ID_33818 Human_SNP_ID_501546373 A-to-I Human chr12 - 53176949 53176949 53176949 AGGTGGGAGGATTGCTTGAAGCCAAGAGTTTAAGACCAGCCTGGGCAACATAGTGAGACCCTGTT AGGTGGGAGGATTGCTTGAAGCCAAGAGTTTAGGACCAGCCTGGGCAACATAGTGAGACCCTGTT T C CSAD Ensembl:ENSG00000139631 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1434137362 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25024178 33819 RMVar_ID_33819 Human_SNP_ID_501546384 A-to-I Human chr12 - 53177010 53177010 53177010 ACATTATATTTTGGCCAGGCGAGGTGGCTCACACCTGTAATCCCAGTGCTTTGGGAGGCTGAGGT ACATTATATTTTGGCCAGGCGAGGTGGCTCACGCCTGTAATCCCAGTGCTTTGGGAGGCTGAGGT T C CSAD Ensembl:ENSG00000139631 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1258914142 Functional Loss SNV dbSNP153 33..33 33 - - - 33820 RMVar_ID_33820 Human_SNP_ID_501546527 A-to-I Human chr12 - 53177584 53177584 53177584 CTCCACGCTTTGTTGCCTTAGGCTGGTTTCCAACTCGTGAGCTCAAGTGATCCTCCCACTTCAGC CTCCACGCTTTGTTGCCTTAGGCTGGTTTCCAGCTCGTGAGCTCAAGTGATCCTCCCACTTCAGC T C CSAD Ensembl:ENSG00000139631 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1136356 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8378569,Human_RBP_ID_11973444 33821 RMVar_ID_33821 Human_SNP_ID_501546579 A-to-I Human chr12 - 53177770 53177770 53177770 AGCTGGGCTTGGTGGCACGTGCCTGTAATCCCAGTTACCAGGTGGCTGAGGCAGGAGAATCACTT AGCTGGGCTTGGTGGCACGTGCCTGTAATCCCCGTTACCAGGTGGCTGAGGCAGGAGAATCACTT T G CSAD Ensembl:ENSG00000139631 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1296141390 Functional Loss SNV dbSNP153 33..33 33 - - - 33822 RMVar_ID_33822 Human_SNP_ID_501546580 A-to-I Human chr12 - 53177775 53177775 53177775 AAATTAGCTGGGCTTGGTGGCACGTGCCTGTAATCCCAGTTACCAGGTGGCTGAGGCAGGAGAAT AAATTAGCTGGGCTTGGTGGCACGTGCCTGTAGTCCCAGTTACCAGGTGGCTGAGGCAGGAGAAT T C CSAD Ensembl:ENSG00000139631 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1003850410 Functional Loss SNV dbSNP153 33..33 33 - - - 33823 RMVar_ID_33823 Human_SNP_ID_501546606 A-to-I Human chr12 - 53177912 53177912 53177912 TCTCTGGACAGGCACGGTGGCTCACGCCTGTAATCCCAGCACTCTGGGAGACCGAGGTGGGCGGA TCTCTGGACAGGCACGGTGGCTCACGCCTGTATTCCCAGCACTCTGGGAGACCGAGGTGGGCGGA T A CSAD Ensembl:ENSG00000139631 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1302191023 Functional Loss SNV dbSNP153 33..33 33 - - - 33824 RMVar_ID_33824 Human_SNP_ID_501546675 A-to-I Human chr12 - 53178216 53178216 53178216 CATTGGCCTCGGCCTCCTAGAGTGCTAGGATTACAGGATTGAGCCACCATGCCTGGCCGGATATG CATTGGCCTCGGCCTCCTAGAGTGCTAGGATTGCAGGATTGAGCCACCATGCCTGGCCGGATATG T C CSAD Ensembl:ENSG00000139631 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs1032073051 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11973451,Human_RBP_ID_25024181 33825 RMVar_ID_33825 Human_SNP_ID_501546687 A-to-I Human chr12 - 53178251 53178251 53178251 CCAGGCTGGTCTCGAATTCCTAGGCTCAAGCTATCCATTGGCCTCGGCCTCCTAGAGTGCTAGGA CCAGGCTGGTCTCGAATTCCTAGGCTCAAGCTGTCCATTGGCCTCGGCCTCCTAGAGTGCTAGGA T C CSAD Ensembl:ENSG00000139631 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs984262069 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11973452 33826 RMVar_ID_33826 Human_SNP_ID_501546690 A-to-I Human chr12 - 53178262 53178262 53178262 TGCCATGTTGCCCAGGCTGGTCTCGAATTCCTAGGCTCAAGCTATCCATTGGCCTCGGCCTCCTA TGCCATGTTGCCCAGGCTGGTCTCGAATTCCTGGGCTCAAGCTATCCATTGGCCTCGGCCTCCTA T C CSAD Ensembl:ENSG00000139631 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1565680783 Functional Loss SNV dbSNP153 33..33 33 - - - 33827 RMVar_ID_33827 Human_SNP_ID_501546731 A-to-I Human chr12 - 53178370 53178370 53178370 CTCCCATCTTAGCCTCCCAAGTAGTTGGGACTACAGATGTGGGCAACTGTGCCTGGATAATTTTG CTCCCATCTTAGCCTCCCAAGTAGTTGGGACTGCAGATGTGGGCAACTGTGCCTGGATAATTTTG T C CSAD Ensembl:ENSG00000139631 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs968470779 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11973456 33828 RMVar_ID_33828 Human_SNP_ID_501546784 A-to-I Human chr12 - 53178548 53178542 53178549 ACCTCAGGTCATCTACCCACCTTGGCCTCCCAAAGTGCTGGGATTCCAGGTGTGAGCCACCACAC ACCTCAGGTCATCTACCCACCTTGGCCTCCC_______TGGGATTCCAGGTGTGAGCCACCACAC AGCACTTT A CSAD Ensembl:ENSG00000139631 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1269563379 Functional Loss DEL dbSNP153 32..38 33 - - - 33829 RMVar_ID_33829 Human_SNP_ID_501546786 A-to-I Human chr12 - 53178548 53178546 53178548 ACCTCAGGTCATCTACCCACCTTGGCCTCCCAAAGTGCTGGGATTCCAGGTGTGAGCCACCACAC ACCTCAGGTCATCTACCCACCTTGGCCTCCCA__GTGCTGGGATTCCAGGTGTGAGCCACCACAC CTT C CSAD Ensembl:ENSG00000139631 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1357194855 Functional Loss DEL dbSNP153 33..34 33 - - - 33830 RMVar_ID_33830 Human_SNP_ID_501546843 A-to-I Human chr12 - 53178794 53178788 53178794 ATGTGCTTTTATTTAAATTTATTTTTATTTTTATTTTTTTTTGAGATGGAGTCTCACTCTGTCAC ATGTGCTTTTATTTAAATTTATTTTTATTTTT______TTTTGAGATGGAGTCTCACTCTGTCAC AAAAAAT A CSAD Ensembl:ENSG00000139631 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs201098413 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_6195963 33831 RMVar_ID_33831 Human_SNP_ID_501546845 A-to-I Human chr12 - 53178794 53178794 53178794 ATGTGCTTTTATTTAAATTTATTTTTATTTTTATTTTTTTTTGAGATGGAGTCTCACTCTGTCAC ATGTGCTTTTATTTAAATTTATTTTTATTTTTTTTTTTTTTTGAGATGGAGTCTCACTCTGTCAC T A CSAD Ensembl:ENSG00000139631 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1207974949 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6195963 33832 RMVar_ID_33832 Human_SNP_ID_501546917 A-to-I Human chr12 - 53179108 53179108 53179108 TGGCTCACACCTGTAATCCCAGCACGTTGGGAAGCCGAGGTGGGCGGATCATCTGAGGTCGGGAG TGGCTCACACCTGTAATCCCAGCACGTTGGGAGGCCGAGGTGGGCGGATCATCTGAGGTCGGGAG T C CSAD Ensembl:ENSG00000139631 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs369618895 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11973465 Human_Splice_Rec_1373872,Human_Splice_Rec_1373891 33833 RMVar_ID_33833 Human_SNP_ID_501548760 A-to-I Human chr12 + 53184390 53184390 53184390 CTTGTATTTTTAGTATAGACAAGGTTTCACCTATTGTCCAGGCTTGTCTCGAACTCCTGACTTCG CTTGTATTTTTAGTATAGACAAGGTTTCACCTGTTGTCCAGGCTTGTCTCGAACTCCTGACTTCG A G ZNF740 Ensembl:ENSG00000139651 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1273044556 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23564368 RMVar_hsa_circ_356124 33834 RMVar_ID_33834 Human_SNP_ID_501548792 A-to-I Human chr12 + 53184447 53184447 53184447 TGACTTCGTGATCCGCCCGCCTCATTCTCCCAAAGTGCTGGGATTATAGGTGTGAGCCACTGCAC TGACTTCGTGATCCGCCCGCCTCATTCTCCCAGAGTGCTGGGATTATAGGTGTGAGCCACTGCAC A G ZNF740 Ensembl:ENSG00000139651 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1435214890 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_356124 33835 RMVar_ID_33835 Human_SNP_ID_501554110 A-to-I Human chr12 - 53202451 53202451 53202451 ACTTGGGCGCCTGAGGCCAGAGAATTGCTTGAATCTGGGAGGCAGAGGTTGCAGTGAGCTGAGAT ACTTGGGCGCCTGAGGCCAGAGAATTGCTTGAGTCTGGGAGGCAGAGGTTGCAGTGAGCTGAGAT T C ITGB7 Ensembl:ENSG00000139626 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1005436775 Functional Loss SNV dbSNP153 33..33 33 - - - 33836 RMVar_ID_33836 Human_SNP_ID_501554176 A-to-I Human chr12 - 53202773 53202773 53202773 TATTTTTAGTAGAGACGGGGTTTCACTATGTTAGCCAGGCTGGTCTTGAACTCCTGACCTTGTGA TATTTTTAGTAGAGACGGGGTTTCACTATGTTGGCCAGGCTGGTCTTGAACTCCTGACCTTGTGA T C ITGB7 Ensembl:ENSG00000139626 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1365249008 Functional Loss SNV dbSNP153 33..33 33 - - - 33837 RMVar_ID_33837 Human_SNP_ID_501554558 A-to-I Human chr12 - 53204214 53204214 53204214 CACCATGCCTGGATAATTTTTGTATTTTTAGTAGATATGGGGTTTCACCATGTTGGTATGGCTGG CACCATGCCTGGATAATTTTTGTATTTTTAGTGGATATGGGGTTTCACCATGTTGGTATGGCTGG T C ITGB7 Ensembl:ENSG00000139626 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs139564701 Functional Loss SNV dbSNP153 33..33 33 - - - 33838 RMVar_ID_33838 Human_SNP_ID_501574776 A-to-I Human chr12 + 53281678 53281678 53281678 ACTCCGAAGGCCCTGGGTATTAGAAAGAATTTAGGATTTTCTTGATATTTGCCTGGCTTTTGAGA ACTCCGAAGGCCCTGGGTATTAGAAAGAATTTGGGATTTTCTTGATATTTGCCTGGCTTTTGAGA A G ESPL1 Ensembl:ENSG00000135476 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs768172628 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19058216 RMVar_hsa_circ_123069,RMVar_hsa_circ_156888,RMVar_hsa_circ_9623,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_113745,RMVar_hsa_circ_156894,RMVar_hsa_circ_90320,RMVar_hsa_circ_156897,RMVar_hsa_circ_370133,RMVar_hsa_circ_156899 33839 RMVar_ID_33839 Human_SNP_ID_501574779 A-to-I Human chr12 + 53281692 53281692 53281692 GGGTATTAGAAAGAATTTAGGATTTTCTTGATATTTGCCTGGCTTTTGAGATTTCCCTGGAGCTA GGGTATTAGAAAGAATTTAGGATTTTCTTGATTTTTGCCTGGCTTTTGAGATTTCCCTGGAGCTA A T ESPL1 Ensembl:ENSG00000135476 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs894832345 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19058216 RMVar_hsa_circ_123069,RMVar_hsa_circ_156888,RMVar_hsa_circ_9623,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_113745,RMVar_hsa_circ_156894,RMVar_hsa_circ_90320,RMVar_hsa_circ_156897,RMVar_hsa_circ_370133,RMVar_hsa_circ_156899 33840 RMVar_ID_33840 Human_SNP_ID_501574859 A-to-I Human chr12 + 53282043 53282043 53282043 GTTTTTATCATTCCTAAATTGGCGGACAAGTCACTGGTGAGGGCAAAGCTAGGAACTGTTACTGC GTTTTTATCATTCCTAAATTGGCGGACAAGTCGCTGGTGAGGGCAAAGCTAGGAACTGTTACTGC A G ESPL1 Ensembl:ENSG00000135476 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs569783804 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123069,RMVar_hsa_circ_156888,RMVar_hsa_circ_9623,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_113745,RMVar_hsa_circ_156894,RMVar_hsa_circ_90320,RMVar_hsa_circ_156897,RMVar_hsa_circ_370133,RMVar_hsa_circ_156899 33841 RMVar_ID_33841 Human_SNP_ID_501574862 A-to-I Human chr12 + 53282061 53282061 53282061 TTGGCGGACAAGTCACTGGTGAGGGCAAAGCTAGGAACTGTTACTGCTTCTCAGGGTCAGGAACA TTGGCGGACAAGTCACTGGTGAGGGCAAAGCTGGGAACTGTTACTGCTTCTCAGGGTCAGGAACA A G ESPL1 Ensembl:ENSG00000135476 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1432123190 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123069,RMVar_hsa_circ_156888,RMVar_hsa_circ_9623,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_113745,RMVar_hsa_circ_156894,RMVar_hsa_circ_90320,RMVar_hsa_circ_156897,RMVar_hsa_circ_370133,RMVar_hsa_circ_156899 33842 RMVar_ID_33842 Human_SNP_ID_501575387 A-to-I Human chr12 + 53284284 53284284 53284284 CTTTTTTTATTTTTGAGACAGAGTCTCACTTTATTACCCAGGCTGGAGTGCAGTGGCGTGATCTT CTTTTTTTATTTTTGAGACAGAGTCTCACTTTCTTACCCAGGCTGGAGTGCAGTGGCGTGATCTT A C ESPL1 Ensembl:ENSG00000135476 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1306617822 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123069,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_113745,RMVar_hsa_circ_156894,RMVar_hsa_circ_90320,RMVar_hsa_circ_156897,RMVar_hsa_circ_156900,RMVar_hsa_circ_375084 33843 RMVar_ID_33843 Human_SNP_ID_501578816 A-to-I Human chr12 - 53296275 53296275 53296275 GCAGCAGGTAGCCGTTCCTGTGGAAAGGATACAGAACTCGTCAGTGGGACGAGTAATTCTTTCCC GCAGCAGGTAGCCGTTCCTGTGGAAAGGATACTGAACTCGTCAGTGGGACGAGTAATTCTTTCCC T A - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs760941908 Functional Loss SNV dbSNP153 33..33 33 - - - 33844 RMVar_ID_33844 Human_SNP_ID_501578817 A-to-I Human chr12 - 53296275 53296275 53296275 GCAGCAGGTAGCCGTTCCTGTGGAAAGGATACAGAACTCGTCAGTGGGACGAGTAATTCTTTCCC GCAGCAGGTAGCCGTTCCTGTGGAAAGGATACGGAACTCGTCAGTGGGACGAGTAATTCTTTCCC T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs760941908 Functional Loss SNV dbSNP153 33..33 33 - - - 33845 RMVar_ID_33845 Human_SNP_ID_501578893 A-to-I Human chr12 + 53296434 53296426 53296434 CCCTTTTTTTTTTTCTTTCTTTTTTGAGACGGAATTTCGCTCTGTCGCCCAGGCTGGAGCGCAAT CCCTTTTTTTTTTTCTTTCTTTTTT________ATTTCGCTCTGTCGCCCAGGCTGGAGCGCAAT TGAGACGGA T PFDN5 Ensembl:ENSG00000123349 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404399359 Functional Loss DEL dbSNP153 26..33 33 - - - Human_RBP_ID_11974176,Human_RBP_ID_24979146 Human_Splice_Rec_1374582,Human_Splice_Rec_1374584,Human_Splice_Rec_1374606,Human_Splice_Rec_1374610,Human_Splice_Rec_1374657,Human_Splice_Rec_1374662,Human_Splice_Rec_1374663 RMVar_hsa_circ_26175,RMVar_hsa_circ_100047,RMVar_hsa_circ_156904,RMVar_hsa_circ_101607,RMVar_hsa_circ_156906 33846 RMVar_ID_33846 Human_SNP_ID_501578918 A-to-I Human chr12 + 53296488 53296488 53296488 TGGAGCGCAATGGTGAGATCTTGGCTTACTGCAACCTCCGCCTCCCGAGTTCAAGAGATTCTTCT TGGAGCGCAATGGTGAGATCTTGGCTTACTGCGACCTCCGCCTCCCGAGTTCAAGAGATTCTTCT A G PFDN5 Ensembl:ENSG00000123349 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223937067 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1374582,Human_Splice_Rec_1374584,Human_Splice_Rec_1374585,Human_Splice_Rec_1374606,Human_Splice_Rec_1374610,Human_Splice_Rec_1374616,Human_Splice_Rec_1374617,Human_Splice_Rec_1374646,Human_Splice_Rec_1374647,Human_Splice_Rec_1374662 RMVar_hsa_circ_26175,RMVar_hsa_circ_100047,RMVar_hsa_circ_156904,RMVar_hsa_circ_101607,RMVar_hsa_circ_156906 33847 RMVar_ID_33847 Human_SNP_ID_501578935 A-to-I Human chr12 + 53296538 53296538 53296538 TCAAGAGATTCTTCTGCCTCAGTCTCCCGAGTAGCTGGGACTTTAGGTACGCGCCACCACGACCG TCAAGAGATTCTTCTGCCTCAGTCTCCCGAGTGGCTGGGACTTTAGGTACGCGCCACCACGACCG A G PFDN5 Ensembl:ENSG00000123349 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs559518337 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1374585,Human_Splice_Rec_1374616,Human_Splice_Rec_1374617,Human_Splice_Rec_1374646,Human_Splice_Rec_1374647 RMVar_hsa_circ_26175,RMVar_hsa_circ_100047,RMVar_hsa_circ_156904,RMVar_hsa_circ_101607,RMVar_hsa_circ_156906 33848 RMVar_ID_33848 Human_SNP_ID_501579099 A-to-I Human chr12 + 53297273 53297273 53297273 CAACATGGTGAAACCCTGTCTTTACTAAATATACAAAAATTAGCCAGGCGTGGTGGCACATGCTT CAACATGGTGAAACCCTGTCTTTACTAAATATGCAAAAATTAGCCAGGCGTGGTGGCACATGCTT A G PFDN5 Ensembl:ENSG00000123349 Protein coding intron GSE38233;GSE99789 cultured B-cells;esophageal squamous carcinoma cells,EC109 - 24183664,29796672 RNA-Seq:(High) rs1228926800 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26175,RMVar_hsa_circ_100047,RMVar_hsa_circ_156904,RMVar_hsa_circ_101607,RMVar_hsa_circ_156906 33849 RMVar_ID_33849 Human_SNP_ID_501579134 A-to-I Human chr12 + 53297399 53297399 53297399 TGCAGTGAGCCGATAGCGGGCAATTGCACTCCAACCTGGGCGATAGAGCGAGACTCTGTCTCAGA TGCAGTGAGCCGATAGCGGGCAATTGCACTCCCACCTGGGCGATAGAGCGAGACTCTGTCTCAGA A C PFDN5 Ensembl:ENSG00000123349 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs551812145 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11974208 Human_Splice_Rec_1374658 RMVar_hsa_circ_26175,RMVar_hsa_circ_100047,RMVar_hsa_circ_156904,RMVar_hsa_circ_101607,RMVar_hsa_circ_156906 33850 RMVar_ID_33850 Human_SNP_ID_501579135 A-to-I Human chr12 + 53297399 53297399 53297399 TGCAGTGAGCCGATAGCGGGCAATTGCACTCCAACCTGGGCGATAGAGCGAGACTCTGTCTCAGA TGCAGTGAGCCGATAGCGGGCAATTGCACTCCGACCTGGGCGATAGAGCGAGACTCTGTCTCAGA A G PFDN5 Ensembl:ENSG00000123349 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs551812145 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11974208 Human_Splice_Rec_1374658 RMVar_hsa_circ_26175,RMVar_hsa_circ_100047,RMVar_hsa_circ_156904,RMVar_hsa_circ_101607,RMVar_hsa_circ_156906 33851 RMVar_ID_33851 Human_SNP_ID_501605058 A-to-I Human chr12 + 53389527 53389527 53389527 CACTGTGCCCAGCCGCTAATTTTTGCATTTTTAGTAGAGACTGGGTTTCACCATGTTGGCCAGGA CACTGTGCCCAGCCGCTAATTTTTGCATTTTTGGTAGAGACTGGGTTTCACCATGTTGGCCAGGA A G SP1 Ensembl:ENSG00000185591 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1259551751 Functional Loss SNV dbSNP153 33..33 33 - - - 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_156939 33852 RMVar_ID_33852 Human_SNP_ID_501621164 A-to-I Human chr12 + 53445132 53445131 53445132 CCAGCACTTTGGGATTCCGGGGCGGGCGGATCACGAGGTCAGGAGTTCAAGACCAGCCTAGCCAA CCAGCACTTTGGGATTCCGGGGCGGGCGGATC_CGAGGTCAGGAGTTCAAGACCAGCCTAGCCAA CA C PRR13,AC023509.1 Ensembl:ENSG00000205352,Ensembl:ENSG00000257379 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1377880563 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_95847,RMVar_hsa_circ_99716,RMVar_hsa_circ_156944,RMVar_hsa_circ_82729,RMVar_hsa_circ_156945,RMVar_hsa_circ_78908,RMVar_hsa_circ_156946,RMVar_hsa_circ_156947 33853 RMVar_ID_33853 Human_SNP_ID_501621170 A-to-I Human chr12 + 53445159 53445159 53445159 GGATCACGAGGTCAGGAGTTCAAGACCAGCCTAGCCAACATGGTGAAACCTGTCTACTAAAGATA GGATCACGAGGTCAGGAGTTCAAGACCAGCCTCGCCAACATGGTGAAACCTGTCTACTAAAGATA A C PRR13,AC023509.1 Ensembl:ENSG00000205352,Ensembl:ENSG00000257379 Protein coding,lincRNA intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1423898949 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95847,RMVar_hsa_circ_99716,RMVar_hsa_circ_156944,RMVar_hsa_circ_82729,RMVar_hsa_circ_156945,RMVar_hsa_circ_78908,RMVar_hsa_circ_156946,RMVar_hsa_circ_156947 33854 RMVar_ID_33854 Human_SNP_ID_501622456 A-to-I Human chr12 + 53450010 53450010 53450010 CTGATACTGCGCCACTGTACTCCAGCCGAGGCAACAGAGTGAGACTCCGTCTCAAAAAAAAAAGA CTGATACTGCGCCACTGTACTCCAGCCGAGGCTACAGAGTGAGACTCCGTCTCAAAAAAAAAAGA A T AC023509.1 Ensembl:ENSG00000257379 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1191504023 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82729,RMVar_hsa_circ_156946 33855 RMVar_ID_33855 Human_SNP_ID_501624663 A-to-I Human chr12 + 53456337 53456337 53456337 AGAATTAGCTGGGCATGGTGGTGTGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAGATAGGAGA AGAATTAGCTGGGCATGGTGGTGTGCGCCTGTGATCCCAGCTACTCAGGAGGCTGAGATAGGAGA A G PCBP2,AC023509.1 Ensembl:ENSG00000197111,Ensembl:ENSG00000257379 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs901237988 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36422,RMVar_hsa_circ_82729,RMVar_hsa_circ_156946,RMVar_hsa_circ_295324,RMVar_hsa_circ_354734,RMVar_hsa_circ_369829,RMVar_hsa_circ_312833,RMVar_hsa_circ_274363,RMVar_hsa_circ_156950,RMVar_hsa_circ_56429,RMVar_hsa_circ_156952,RMVar_hsa_circ_156951,RMVar_hsa_circ_124300,RMVar_hsa_circ_64066,RMVar_hsa_circ_125173,RMVar_hsa_circ_156953,RMVar_hsa_circ_270150,RMVar_hsa_circ_368867,RMVar_hsa_circ_156954,RMVar_hsa_circ_365218,RMVar_hsa_circ_73434,RMVar_hsa_circ_156956 33856 RMVar_ID_33856 Human_SNP_ID_501628773 A-to-I Human chr12 + 53469068 53469068 53469068 GGGATTACAGGCATGTGCCACCATGCCTGGCTAATTTTGTATTTTTAGTAGAGATGGAGTTTCTC GGGATTACAGGCATGTGCCACCATGCCTGGCTGATTTTGTATTTTTAGTAGAGATGGAGTTTCTC A G PCBP2 Ensembl:ENSG00000197111 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1424442402 Functional Loss SNV dbSNP153 33..33 33 - - - 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 33857 RMVar_ID_33857 Human_SNP_ID_501629027 A-to-I Human chr12 + 53469841 53469841 53469841 TTGGCTCACTGTGACCTCCGTCTCCTGGGTTCAAGCAATTTTCCTGCCCCAGCCTCCCGAGTAGA TTGGCTCACTGTGACCTCCGTCTCCTGGGTTCTAGCAATTTTCCTGCCCCAGCCTCCCGAGTAGA A T PCBP2 Ensembl:ENSG00000197111 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1291191625 Functional Loss SNV dbSNP153 33..33 33 - - - 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 33858 RMVar_ID_33858 Human_SNP_ID_501629142 A-to-I Human chr12 + 53470157 53470157 53470157 ATATAATCCCAGCACTTGTGGGAGGCTGAGGCAAGTGGGTCACGAGGTCAGGAGACCAGCCTGAC ATATAATCCCAGCACTTGTGGGAGGCTGAGGCGAGTGGGTCACGAGGTCAGGAGACCAGCCTGAC A G PCBP2 Ensembl:ENSG00000197111 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs577544496 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11976074,Human_RBP_ID_17561142,Human_RBP_ID_17821835,Human_RBP_ID_25024336 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 33859 RMVar_ID_33859 Human_SNP_ID_501629285 A-to-I Human chr12 + 53470458 53470457 53470459 AAAGGGTCTCCCTCTGTTGCCCAGGCTGGAGCAGAGAGGCATGATCGTGGCTCACTGCAGCCTTG AAAGGGTCTCCCTCTGTTGCCCAGGCTGGAGC__AGAGGCATGATCGTGGCTCACTGCAGCCTTG CAG C PCBP2 Ensembl:ENSG00000197111 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1565869868 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_11976077,Human_RBP_ID_17561143 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 33860 RMVar_ID_33860 Human_SNP_ID_501629286 A-to-I Human chr12 + 53470458 53470458 53470458 AAAGGGTCTCCCTCTGTTGCCCAGGCTGGAGCAGAGAGGCATGATCGTGGCTCACTGCAGCCTTG AAAGGGTCTCCCTCTGTTGCCCAGGCTGGAGCGGAGAGGCATGATCGTGGCTCACTGCAGCCTTG A G PCBP2 Ensembl:ENSG00000197111 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1239888233 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11976077,Human_RBP_ID_17561143 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 33861 RMVar_ID_33861 Human_SNP_ID_501629594 A-to-I Human chr12 + 53471318 53471318 53471318 TTTTTTTTAAAGGGCCAGGTTCGGTGGCTTATACCTGTAATCCCAGCACTTTGGGAGGCCAAGGT TTTTTTTTAAAGGGCCAGGTTCGGTGGCTTATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGT A G PCBP2 Ensembl:ENSG00000197111 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs554985008 Functional Loss SNV dbSNP153 33..33 33 - - - 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 33862 RMVar_ID_33862 Human_SNP_ID_501629641 A-to-I Human chr12 + 53471490 53471490 53471490 GTCCTGCTGAGGCAGGTGAATTGCTCAAATCCAGGAGGCTGAGGTTGCACAGTGAGCCAAGATCA GTCCTGCTGAGGCAGGTGAATTGCTCAAATCCGGGAGGCTGAGGTTGCACAGTGAGCCAAGATCA A G PCBP2 Ensembl:ENSG00000197111 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1011290497 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6196941 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 33863 RMVar_ID_33863 Human_SNP_ID_501631883 A-to-I Human chr12 + 53478397 53478397 53478397 GGGCATGGTGACAGCTGCCTGGAATTGCAGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTAGAA GGGCATGGTGACAGCTGCCTGGAATTGCAGCTCCTCAGGAGGCTGAGGCAGGAGAATCGCTAGAA A C PCBP2 Ensembl:ENSG00000197111 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1353932861 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11976572,Human_RBP_ID_24980004 RMVar_hsa_circ_127496,RMVar_hsa_circ_156968 33864 RMVar_ID_33864 Human_SNP_ID_501635182 A-to-I Human chr12 + 53488580 53488580 53488580 CTACTTGGGAGGCTGAGGCAGAAGAATTGCTTAAACCCGGGAGGCTGAGGTTTTGGTGAGCCAAG CTACTTGGGAGGCTGAGGCAGAAGAATTGCTTGAACCCGGGAGGCTGAGGTTTTGGTGAGCCAAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs761080916 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8378940 33865 RMVar_ID_33865 Human_SNP_ID_501635183 A-to-I Human chr12 + 53488580 53488580 53488580 CTACTTGGGAGGCTGAGGCAGAAGAATTGCTTAAACCCGGGAGGCTGAGGTTTTGGTGAGCCAAG CTACTTGGGAGGCTGAGGCAGAAGAATTGCTTTAACCCGGGAGGCTGAGGTTTTGGTGAGCCAAG A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs761080916 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8378940 33866 RMVar_ID_33866 Human_SNP_ID_501642627 A-to-I Human chr12 - 53518009 53518009 53518009 AATTCAAAAATTAGCCAGGTGTGGCAGTGTGCACCTGTAGTCCCAGCTACTCGGAAGGCTGAGGC AATTCAAAAATTAGCCAGGTGTGGCAGTGTGCGCCTGTAGTCCCAGCTACTCGGAAGGCTGAGGC T C ATF7-NPFF,ATF7 Ensembl:ENSG00000267281,Ensembl:ENSG00000170653 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917371210 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80477,RMVar_hsa_circ_125492,RMVar_hsa_circ_90019,RMVar_hsa_circ_89141,RMVar_hsa_circ_156985,RMVar_hsa_circ_156986,RMVar_hsa_circ_156987,RMVar_hsa_circ_156984,RMVar_hsa_circ_55838 33867 RMVar_ID_33867 Human_SNP_ID_501642644 A-to-I Human chr12 - 53518073 53518073 53518073 ATCACTTGAGGTCAGGAGTTTGAGACCAGCCTAGCTAACGTGGCAAAACCCCATCTCTACTAAAA ATCACTTGAGGTCAGGAGTTTGAGACCAGCCTGGCTAACGTGGCAAAACCCCATCTCTACTAAAA T C ATF7-NPFF,ATF7 Ensembl:ENSG00000267281,Ensembl:ENSG00000170653 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1565914178 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80477,RMVar_hsa_circ_125492,RMVar_hsa_circ_90019,RMVar_hsa_circ_89141,RMVar_hsa_circ_156985,RMVar_hsa_circ_156986,RMVar_hsa_circ_156987,RMVar_hsa_circ_156984,RMVar_hsa_circ_55838 33868 RMVar_ID_33868 Human_SNP_ID_501647726 A-to-I Human chr12 - 53540188 53540188 53540188 TGCCACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCTGGC TGCCACCATGCCTGGCTAATTTTTGTATTTTTGGTAGAGACAGGGTTTCACCATGTTGGCCTGGC T C ATF7-NPFF,ATF7 Ensembl:ENSG00000267281,Ensembl:ENSG00000170653 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1169534354 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125492,RMVar_hsa_circ_90019,RMVar_hsa_circ_156986,RMVar_hsa_circ_156987,RMVar_hsa_circ_55838,RMVar_hsa_circ_69330,RMVar_hsa_circ_28254 33869 RMVar_ID_33869 Human_SNP_ID_501647923 A-to-I Human chr12 - 53541011 53541011 53541011 CAGAAAGAGGGCTGCGCGAGGCCTGGTGGTTCACACCTGTAATCCCAGTGCTTAGGGAGGCCACA CAGAAAGAGGGCTGCGCGAGGCCTGGTGGTTCGCACCTGTAATCCCAGTGCTTAGGGAGGCCACA T C ATF7-NPFF,ATF7 Ensembl:ENSG00000267281,Ensembl:ENSG00000170653 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1248167653 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125492,RMVar_hsa_circ_90019,RMVar_hsa_circ_156986,RMVar_hsa_circ_156987,RMVar_hsa_circ_55838,RMVar_hsa_circ_69330,RMVar_hsa_circ_28254 33870 RMVar_ID_33870 Human_SNP_ID_501656494 A-to-I Human chr12 - 53578258 53578258 53578258 GCGATCCTCCCACCTCAGCCTCCCAAATAGCTAGGACTATAGGTACACGCCAGGACACTTGGCTA GCGATCCTCCCACCTCAGCCTCCCAAATAGCTCGGACTATAGGTACACGCCAGGACACTTGGCTA T G ATF7-NPFF,ATF7 Ensembl:ENSG00000267281,Ensembl:ENSG00000170653 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1362244628 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125492,RMVar_hsa_circ_156987,RMVar_hsa_circ_55838,RMVar_hsa_circ_69330,RMVar_hsa_circ_340567,RMVar_hsa_circ_156993 33871 RMVar_ID_33871 Human_SNP_ID_501665071 A-to-I Human chr12 - 53616937 53616937 53616937 TCTCACCTTTTTTTTTTTTTTTTTGGAGACAGAGTCGTTCTCTGTTGCCTAGGCTGGAGTACAGT TCTCACCTTTTTTTTTTTTTTTTTGGAGACAGCGTCGTTCTCTGTTGCCTAGGCTGGAGTACAGT T G ATF7-NPFF,ATF7 Ensembl:ENSG00000267281,Ensembl:ENSG00000170653 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1340375970 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94771,RMVar_hsa_circ_156993,RMVar_hsa_circ_156994 33872 RMVar_ID_33872 Human_SNP_ID_501665180 A-to-I Human chr12 - 53617371 53617371 53617371 CACCCACCTTGACCTCCCCAAGTGCTGGGATTACAGGTGTGAGCCACTGTGCCTGGCCTAGTATA CACCCACCTTGACCTCCCCAAGTGCTGGGATTTCAGGTGTGAGCCACTGTGCCTGGCCTAGTATA T A ATF7-NPFF,ATF7 Ensembl:ENSG00000267281,Ensembl:ENSG00000170653 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941313198 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94771,RMVar_hsa_circ_156993,RMVar_hsa_circ_156994 33873 RMVar_ID_33873 Human_SNP_ID_501676762 A-to-I Human chr12 - 53665291 53665291 53665291 TGCCATGTGAAGGAGCCGTCTCCACCTCCCATAGTTCTCCCGCGTCTGGTTGGCCCCGTGTGTTC TGCCATGTGAAGGAGCCGTCTCCACCTCCCATTGTTCTCCCGCGTCTGGTTGGCCCCGTGTGTTC T A ATP5MC2 Ensembl:ENSG00000135390 Protein coding intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1276052181 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_34762,Human_RBP_ID_228941,Human_RBP_ID_422529,Human_RBP_ID_753661,Human_RBP_ID_876141,Human_RBP_ID_1269729,Human_RBP_ID_1797117,Human_RBP_ID_2343663,Human_RBP_ID_3408552,Human_RBP_ID_4256543,Human_RBP_ID_5437783,Human_RBP_ID_5491674,Human_RBP_ID_8379047,Human_RBP_ID_11978220,Human_RBP_ID_17239203,Human_RBP_ID_17354931,Human_RBP_ID_17474775,Human_RBP_ID_17650371,Human_RBP_ID_17684747,Human_RBP_ID_18628993,Human_RBP_ID_18935340,Human_RBP_ID_19828446,Human_RBP_ID_22437095,Human_RBP_ID_22794522,Human_RBP_ID_23565060,Human_RBP_ID_26806743,Human_RBP_ID_26908030,Human_RBP_ID_27215699,Human_RBP_ID_27423080 Human_miRNA_ID_314879,Human_miRNA_ID_318151,Human_miRNA_ID_2072788,Human_miRNA_ID_2074471,Human_miRNA_ID_3011608,Human_miRNA_ID_3064634 RMVar_hsa_circ_156995,RMVar_hsa_circ_112522,RMVar_hsa_circ_123686,RMVar_hsa_circ_120204,RMVar_hsa_circ_156996,RMVar_hsa_circ_156997 33874 RMVar_ID_33874 Human_SNP_ID_501677191 A-to-I Human chr12 - 53666899 53666899 53666899 CGCTGTCTCCCAGACTGAAGTGCAGTGGCACAATCTCAGCCCACTGCAATCTCTGCCTCCCGGGT CGCTGTCTCCCAGACTGAAGTGCAGTGGCACAGTCTCAGCCCACTGCAATCTCTGCCTCCCGGGT T C ATP5MC2 Ensembl:ENSG00000135390 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1462633504 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11978267,Human_RBP_ID_23305976 RMVar_hsa_circ_123686,RMVar_hsa_circ_120204,RMVar_hsa_circ_156996,RMVar_hsa_circ_156997 33875 RMVar_ID_33875 Human_SNP_ID_501677699 A-to-I Human chr12 - 53668153 53668153 53668153 GAAACCCTGTCTCTGCTAAAAATACAAAAATTAGCCAGGCGTTGTGGTGGGCGCCTGTAGTCCCA GAAACCCTGTCTCTGCTAAAAATACAAAAATTGGCCAGGCGTTGTGGTGGGCGCCTGTAGTCCCA T C ATP5MC2 Ensembl:ENSG00000135390 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1479339415 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123686,RMVar_hsa_circ_120204,RMVar_hsa_circ_156996,RMVar_hsa_circ_156997 33876 RMVar_ID_33876 Human_SNP_ID_501678792 A-to-I Human chr12 - 53672252 53672252 53672252 GCACCACTGCACTCCAGCCTGGGCGTCAGAGCAAGACTCTGTCTCAAAAAATAAATAAATAAGTA GCACCACTGCACTCCAGCCTGGGCGTCAGAGCGAGACTCTGTCTCAAAAAATAAATAAATAAGTA T C ATP5MC2 Ensembl:ENSG00000135390 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1022985483 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6197686 RMVar_hsa_circ_303241,RMVar_hsa_circ_157000,RMVar_hsa_circ_372062,RMVar_hsa_circ_157002 33877 RMVar_ID_33877 Human_SNP_ID_501678826 A-to-I Human chr12 - 53672386 53672386 53672386 GAAACCCCATCTCTACTAAAAAAACGAAAACCAGTTGGGCATGGTGGCGGGCGCCTGTAATCCCA GAAACCCCATCTCTACTAAAAAAACGAAAACCCGTTGGGCATGGTGGCGGGCGCCTGTAATCCCA T G ATP5MC2 Ensembl:ENSG00000135390 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1419061537 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25024423 RMVar_hsa_circ_303241,RMVar_hsa_circ_157000,RMVar_hsa_circ_372062,RMVar_hsa_circ_157002 33878 RMVar_ID_33878 Human_SNP_ID_501690924 A-to-I Human chr12 - 53718621 53718621 53718621 AGGAAGCTGAGGTGGAAGGATTGCTTGAGCCCAGGAGGTCAAGGCTGCAGTGTGCTGTGATCGCA AGGAAGCTGAGGTGGAAGGATTGCTTGAGCCCGGGAGGTCAAGGCTGCAGTGTGCTGTGATCGCA T C CALCOCO1 Ensembl:ENSG00000012822 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965426846 Functional Loss SNV dbSNP153 33..33 33 - - - 33879 RMVar_ID_33879 Human_SNP_ID_501806616 A-to-I Human chr12 - 54182609 54182609 54182609 CTCTCTCCTTCCTCACAGGTGCCCTTTGGGGAAGTAAGCATGGTCCGGGACTGGTTGGGCATTGT CTCTCTCCTTCCTCACAGGTGCCCTTTGGGGAGGTAAGCATGGTCCGGGACTGGTTGGGCATTGT T C SMUG1 Ensembl:ENSG00000123415 Protein coding intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1184255235 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_877047,Human_RBP_ID_25016955,Human_RBP_ID_26422303 Human_Splice_Rec_1376834,Human_Splice_Rec_1376846,Human_Splice_Rec_1376860,Human_Splice_Rec_1376866,Human_Splice_Rec_1376872,Human_Splice_Rec_1376880,Human_Splice_Rec_1376892,Human_Splice_Rec_1376896,Human_Splice_Rec_1376902,Human_Splice_Rec_1376906,Human_Splice_Rec_1376910,Human_Splice_Rec_1376914,Human_Splice_Rec_1376922,Human_Splice_Rec_1376924,Human_Splice_Rec_1376930 RMVar_hsa_circ_352229,RMVar_hsa_circ_66280,RMVar_hsa_circ_104034,RMVar_hsa_circ_276429,RMVar_hsa_circ_157009,RMVar_hsa_circ_330801 33880 RMVar_ID_33880 Human_SNP_ID_501820958 A-to-I Human chr12 - 54240499 54240499 54240499 TTCATGGCCAGGCACAGTGGCTACCGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGAGAA TTCATGGCCAGGCACAGTGGCTACCGCCTGTAGTCCCAGCACTTTGGGAGGCTGAGGCAGGAGAA T C CBX5 Ensembl:ENSG00000094916 Protein coding 3'UTR GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831 HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line - 29129909,29796672,31158229,32596459 RNA-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 33881 RMVar_ID_33881 Human_SNP_ID_501822064 A-to-I Human chr12 - 54245087 54245087 54245087 TAATTGCTTGAACCTGGGAGGCAGAGGTTGCAATGAGCTGAGATCGAGCCTCTGCACTCCTGCCT TAATTGCTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCTGAGATCGAGCCTCTGCACTCCTGCCT T C CBX5 Ensembl:ENSG00000094916 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs867467540 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112121,RMVar_hsa_circ_114284,RMVar_hsa_circ_157011,RMVar_hsa_circ_157012,RMVar_hsa_circ_157018,RMVar_hsa_circ_378226 33882 RMVar_ID_33882 Human_SNP_ID_501822113 A-to-I Human chr12 - 54245283 54245274 54245283 ATAAAGGTCGGATGCAGTGGCTCACACCTGTAATCCCAACACTTTGGGTGGCCAAGGCAGGCGGA ATAAAGGTCGGATGCAGTGGCTCACACCTGTA_________CTTTGGGTGGCCAAGGCAGGCGGA GTGTTGGGAT G CBX5 Ensembl:ENSG00000094916 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1212428869 Functional Loss DEL dbSNP153 33..41 33 - - - RMVar_hsa_circ_112121,RMVar_hsa_circ_114284,RMVar_hsa_circ_157011,RMVar_hsa_circ_157012,RMVar_hsa_circ_157018,RMVar_hsa_circ_378226 33883 RMVar_ID_33883 Human_SNP_ID_501829713 A-to-I Human chr12 - 54275823 54275823 54275823 CGGCTAATTTTTAGTAGAGACGGGGTTTCTCCATGTTGGTTAGGCTGGCCTCAAACTCCTGACCT CGGCTAATTTTTAGTAGAGACGGGGTTTCTCCTTGTTGGTTAGGCTGGCCTCAAACTCCTGACCT T A CBX5 Ensembl:ENSG00000094916 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs976760960 Functional Loss SNV dbSNP153 33..33 33 - - - 33884 RMVar_ID_33884 Human_SNP_ID_501832955 A-to-I Human chr12 - 54285160 54285160 54285160 CATTCCCATCTATAATTTTATCTGGTACCATTATTCAATTTAGATATATTGCATAGGATGTGCCA CATTCCCATCTATAATTTTATCTGGTACCATTCTTCAATTTAGATATATTGCATAGGATGTGCCA T G - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs766892723 Functional Loss SNV dbSNP153 33..33 33 - - - 33885 RMVar_ID_33885 Human_SNP_ID_501845246 A-to-I Human chr12 + 54332481 54332481 54332481 GGAGGTGGCTGGGCATGGTAGCTCACGCGTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGCGG GGAGGTGGCTGGGCATGGTAGCTCACGCGTGTGATCCCAGCACTTTGGGAGGCTGAGGCAGGCGG A G COPZ1,AC078778.1 Ensembl:ENSG00000111481,Ensembl:ENSG00000258344 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs955353876 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_157050,RMVar_hsa_circ_110639,RMVar_hsa_circ_101848,RMVar_hsa_circ_157049 33886 RMVar_ID_33886 Human_SNP_ID_501845280 A-to-I Human chr12 + 54332623 54332623 54332623 AGGTGTGGTGGTGGGTGCCTGTAATGCCAGCTATTTGAGAGGCTGAGGCAGGAGAATCGCTTGAA AGGTGTGGTGGTGGGTGCCTGTAATGCCAGCTGTTTGAGAGGCTGAGGCAGGAGAATCGCTTGAA A G COPZ1,AC078778.1 Ensembl:ENSG00000111481,Ensembl:ENSG00000258344 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1480606865 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_157050,RMVar_hsa_circ_110639,RMVar_hsa_circ_101848,RMVar_hsa_circ_157049 33887 RMVar_ID_33887 Human_SNP_ID_501845415 A-to-I Human chr12 + 54333226 54333226 54333226 CCACCATGCCCAGCTAATTTTTTTGTATTTTTAGTAGAGACAGGGTTTCGCCATGTTGCCCAGGC CCACCATGCCCAGCTAATTTTTTTGTATTTTTTGTAGAGACAGGGTTTCGCCATGTTGCCCAGGC A T COPZ1,AC078778.1 Ensembl:ENSG00000111481,Ensembl:ENSG00000258344 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1284973871 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_157050,RMVar_hsa_circ_110639,RMVar_hsa_circ_101848,RMVar_hsa_circ_157049 33888 RMVar_ID_33888 Human_SNP_ID_501845424 A-to-I Human chr12 + 54333246 54333246 54333246 TTTTGTATTTTTAGTAGAGACAGGGTTTCGCCATGTTGCCCAGGCTGGCCTCAAACTCCTGAGCT TTTTGTATTTTTAGTAGAGACAGGGTTTCGCCGTGTTGCCCAGGCTGGCCTCAAACTCCTGAGCT A G COPZ1,AC078778.1 Ensembl:ENSG00000111481,Ensembl:ENSG00000258344 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs953444441 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_157050,RMVar_hsa_circ_110639,RMVar_hsa_circ_101848,RMVar_hsa_circ_157049 33889 RMVar_ID_33889 Human_SNP_ID_501845441 A-to-I Human chr12 + 54333322 54333322 54333322 TCCCCACATTGGCCTCCCAAAGTGCTGGTATTACAGGTAGGAACCAGCATGCCTAGCCATGAAAT TCCCCACATTGGCCTCCCAAAGTGCTGGTATTGCAGGTAGGAACCAGCATGCCTAGCCATGAAAT A G COPZ1,AC078778.1 Ensembl:ENSG00000111481,Ensembl:ENSG00000258344 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285442910 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_157050,RMVar_hsa_circ_110639,RMVar_hsa_circ_101848,RMVar_hsa_circ_157049 33890 RMVar_ID_33890 Human_SNP_ID_501846028 A-to-I Human chr12 + 54335749 54335749 54335749 GCTGGAGTGCAGTAGCGCAATTGTAGCTCACTACAGCCTTGAACTCCCAAGCTCAAGCGATCCTC GCTGGAGTGCAGTAGCGCAATTGTAGCTCACTGCAGCCTTGAACTCCCAAGCTCAAGCGATCCTC A G COPZ1,AC078778.1 Ensembl:ENSG00000111481,Ensembl:ENSG00000258344 Protein coding,lincRNA intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1013249709 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_157050,RMVar_hsa_circ_110639,RMVar_hsa_circ_101848,RMVar_hsa_circ_157049 33891 RMVar_ID_33891 Human_SNP_ID_501846072 A-to-I Human chr12 + 54335946 54335946 54335946 AGTGATCTCCTGCCTCAGCTTCCAAAAGTGCTAGGATTACAGGCATGAGCCACTGCGCCTGGCCT AGTGATCTCCTGCCTCAGCTTCCAAAAGTGCTGGGATTACAGGCATGAGCCACTGCGCCTGGCCT A G COPZ1,AC078778.1 Ensembl:ENSG00000111481,Ensembl:ENSG00000258344 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs930816519 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_157050,RMVar_hsa_circ_110639,RMVar_hsa_circ_101848,RMVar_hsa_circ_157049 33892 RMVar_ID_33892 Human_SNP_ID_501846181 A-to-I Human chr12 + 54336420 54336420 54336420 AAAATTAGCCGGGCATGGTGGCAGGTGCGTGTAGTCCCAGCTACTCGGGAGGCTGAAGCAGGAGA AAAATTAGCCGGGCATGGTGGCAGGTGCGTGTGGTCCCAGCTACTCGGGAGGCTGAAGCAGGAGA A G COPZ1,AC078778.1 Ensembl:ENSG00000111481,Ensembl:ENSG00000258344 Protein coding,lincRNA intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs868790330 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_157050,RMVar_hsa_circ_110639,RMVar_hsa_circ_101848,RMVar_hsa_circ_157049 33893 RMVar_ID_33893 Human_SNP_ID_501848704 A-to-I Human chr12 + 54346447 54346447 54346447 GGCACGTGCCACCACGCCTGGCTAATTTTTGTATTTTTAGTGGAGACAGGGTTTTACCATGTTGG GGCACGTGCCACCACGCCTGGCTAATTTTTGTGTTTTTAGTGGAGACAGGGTTTTACCATGTTGG A G COPZ1 Ensembl:ENSG00000111481 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs963181000 Functional Loss SNV dbSNP153 33..33 33 - - - 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 33894 RMVar_ID_33894 Human_SNP_ID_501848711 A-to-I Human chr12 + 54346473 54346473 54346473 TTTTGTATTTTTAGTGGAGACAGGGTTTTACCATGTTGGCCAGGCTGGTCTTGAACTCCTGACCT TTTTGTATTTTTAGTGGAGACAGGGTTTTACCGTGTTGGCCAGGCTGGTCTTGAACTCCTGACCT A G COPZ1 Ensembl:ENSG00000111481 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1376489917 Functional Loss SNV dbSNP153 33..33 33 - - - 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 33895 RMVar_ID_33895 Human_SNP_ID_501880728 A-to-I Human chr12 + 54483532 54483532 54483532 CTCCCACCTCAGCCTCTGGAGTAGCTGGGACTACAGGTGTGTGCCACCTTGCCTGGCTAATTTTT CTCCCACCTCAGCCTCTGGAGTAGCTGGGACTGCAGGTGTGTGCCACCTTGCCTGGCTAATTTTT A G AC079313.2 Ensembl:ENSG00000258137 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048418175 Functional Loss SNV dbSNP153 33..33 33 - - - 33896 RMVar_ID_33896 Human_SNP_ID_502105355 A-to-I Human chr12 - 55328517 55328517 55328517 GAGATCATGCCACTGCAACCTCTGCCTCCCAGATTCAAGCGATTCTCCTGCCTCAGCCTCCTGAG GAGATCATGCCACTGCAACCTCTGCCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1423990520 Functional Loss SNV dbSNP153 33..33 33 - - - 33897 RMVar_ID_33897 Human_SNP_ID_502222333 A-to-I Human chr12 + 55731257 55731257 55731257 ACAATGATGTGTGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCCA ACAATGATGTGTGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCCA A G LOC105369779,LOC105369779:2,LOC105369779:3,LOC105369779:4 RNACentral:URS0000D5D061,RNACentral:URS0000D57932,RNACentral:URS0000D5CF4D,RNACentral:URS0000D5D544 lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048211279 Functional Loss SNV dbSNP153 33..33 33 - - - 33898 RMVar_ID_33898 Human_SNP_ID_502229789 A-to-I Human chr12 - 55762121 55762121 55762121 GGCCATGCTTGGCCAATTTTTGTATGTTTAGTAAAGATGGGTTTCACCATGTTGGCCAGGCTGGT GGCCATGCTTGGCCAATTTTTGTATGTTTAGTGAAGATGGGTTTCACCATGTTGGCCAGGCTGGT T C AC073487.1,AC023055.1,SARNP Ensembl:ENSG00000257509,Ensembl:ENSG00000257390,Ensembl:ENSG00000205323 lincRNA,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1187623157 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36264,RMVar_hsa_circ_35258 33899 RMVar_ID_33899 Human_SNP_ID_502230110 A-to-I Human chr12 - 55763472 55763472 55763472 GAAACCCCATCTCTACTAAAAATACAAAAATTAGGTGTGGTGGCGTGCGCATGTAGTCCCAGCTA GAAACCCCATCTCTACTAAAAATACAAAAATTGGGTGTGGTGGCGTGCGCATGTAGTCCCAGCTA T C AC023055.1,SARNP Ensembl:ENSG00000257390,Ensembl:ENSG00000205323 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1024492549 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36264,RMVar_hsa_circ_35258 33900 RMVar_ID_33900 Human_SNP_ID_502231138 A-to-I Human chr12 - 55767542 55767542 55767542 TGCCCGGCTTGTATTTGTATATTTTTGAGACAAGATCTCACTCTGTTGCCCAGACTGAAGTGCAG TGCCCGGCTTGTATTTGTATATTTTTGAGACAGGATCTCACTCTGTTGCCCAGACTGAAGTGCAG T C AC023055.1,SARNP Ensembl:ENSG00000257390,Ensembl:ENSG00000205323 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1330560530 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11982423 RMVar_hsa_circ_36264,RMVar_hsa_circ_35258 33901 RMVar_ID_33901 Human_SNP_ID_502233128 A-to-I Human chr12 - 55775031 55775031 55775031 TACAAAAAAATTAGTCGGGTGTGGTGGCACACACTTGTAATCCCAGCTATTTGGGAGGCTGAGGC TACAAAAAAATTAGTCGGGTGTGGTGGCACACGCTTGTAATCCCAGCTATTTGGGAGGCTGAGGC T C AC023055.1,SARNP Ensembl:ENSG00000257390,Ensembl:ENSG00000205323 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1006082666 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11982557 RMVar_hsa_circ_36264,RMVar_hsa_circ_35258 33902 RMVar_ID_33902 Human_SNP_ID_502233909 A-to-I Human chr12 - 55778219 55778205 55778220 TTGCTTGAACCGTGGAGGTGGAGGTCTCAGTAAGCTGAGATCATGCCACTGCACTCCAGCCTGGG TTGCTTGAACCGTGGAGGTGGAGGTCTCAGT_______________CACTGCACTCCAGCCTGGG GGCATGATCTCAGCTT G AC023055.1,SARNP Ensembl:ENSG00000257390,Ensembl:ENSG00000205323 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1398005993 Functional Loss DEL dbSNP153 32..46 33 - - - RMVar_hsa_circ_36264,RMVar_hsa_circ_35258 33903 RMVar_ID_33903 Human_SNP_ID_502233909 A-to-I Human chr12 - 55778220 55778205 55778220 ATTGCTTGAACCGTGGAGGTGGAGGTCTCAGTAAGCTGAGATCATGCCACTGCACTCCAGCCTGG ATTGCTTGAACCGTGGAGGTGGAGGTCTCAGT_______________CACTGCACTCCAGCCTGG GGCATGATCTCAGCTT G AC023055.1,SARNP Ensembl:ENSG00000257390,Ensembl:ENSG00000205323 Protein coding,Protein coding intron,intron GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs1398005993 Functional Loss DEL dbSNP153 33..47 33 - - - RMVar_hsa_circ_36264,RMVar_hsa_circ_35258 33904 RMVar_ID_33904 Human_SNP_ID_502233912 A-to-I Human chr12 - 55778219 55778219 55778219 TTGCTTGAACCGTGGAGGTGGAGGTCTCAGTAAGCTGAGATCATGCCACTGCACTCCAGCCTGGG TTGCTTGAACCGTGGAGGTGGAGGTCTCAGTAGGCTGAGATCATGCCACTGCACTCCAGCCTGGG T C AC023055.1,SARNP Ensembl:ENSG00000257390,Ensembl:ENSG00000205323 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1034558170 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36264,RMVar_hsa_circ_35258 33905 RMVar_ID_33905 Human_SNP_ID_502233913 A-to-I Human chr12 - 55778220 55778220 55778220 ATTGCTTGAACCGTGGAGGTGGAGGTCTCAGTAAGCTGAGATCATGCCACTGCACTCCAGCCTGG ATTGCTTGAACCGTGGAGGTGGAGGTCTCAGTGAGCTGAGATCATGCCACTGCACTCCAGCCTGG T C AC023055.1,SARNP Ensembl:ENSG00000257390,Ensembl:ENSG00000205323 Protein coding,Protein coding intron,intron GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs569900801 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36264,RMVar_hsa_circ_35258 33906 RMVar_ID_33906 Human_SNP_ID_502233914 A-to-I Human chr12 - 55778220 55778220 55778220 ATTGCTTGAACCGTGGAGGTGGAGGTCTCAGTAAGCTGAGATCATGCCACTGCACTCCAGCCTGG ATTGCTTGAACCGTGGAGGTGGAGGTCTCAGTCAGCTGAGATCATGCCACTGCACTCCAGCCTGG T G AC023055.1,SARNP Ensembl:ENSG00000257390,Ensembl:ENSG00000205323 Protein coding,Protein coding intron,intron GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs569900801 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36264,RMVar_hsa_circ_35258 33907 RMVar_ID_33907 Human_SNP_ID_502233954 A-to-I Human chr12 - 55778426 55778426 55778426 TAAAGGGGAAACAGGTCAGCACAGTGGCTCACACTTGTAATCTCAGCACTTTGAGAGGCCGAGGC TAAAGGGGAAACAGGTCAGCACAGTGGCTCACGCTTGTAATCTCAGCACTTTGAGAGGCCGAGGC T C AC023055.1,SARNP Ensembl:ENSG00000257390,Ensembl:ENSG00000205323 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs893235337 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36264,RMVar_hsa_circ_35258 33908 RMVar_ID_33908 Human_SNP_ID_502233955 A-to-I Human chr12 - 55778426 55778426 55778426 TAAAGGGGAAACAGGTCAGCACAGTGGCTCACACTTGTAATCTCAGCACTTTGAGAGGCCGAGGC TAAAGGGGAAACAGGTCAGCACAGTGGCTCACCCTTGTAATCTCAGCACTTTGAGAGGCCGAGGC T G AC023055.1,SARNP Ensembl:ENSG00000257390,Ensembl:ENSG00000205323 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs893235337 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36264,RMVar_hsa_circ_35258 33909 RMVar_ID_33909 Human_SNP_ID_502234082 A-to-I Human chr12 - 55778932 55778932 55778932 CAGTCTCGCCCTGTCGCCCAGGCTGGAGTGCAATGGCACGATCTTGGCTCACTGCAACCTCTGCC CAGTCTCGCCCTGTCGCCCAGGCTGGAGTGCAGTGGCACGATCTTGGCTCACTGCAACCTCTGCC T C AC023055.1,SARNP Ensembl:ENSG00000257390,Ensembl:ENSG00000205323 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs920673488 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36264,RMVar_hsa_circ_35258 33910 RMVar_ID_33910 Human_SNP_ID_502234763 A-to-I Human chr12 - 55781870 55781870 55781870 CTCTACAAAAAATAAGAACAGCCAGGCATGGTAGTGAGTGCCGGTAGTCCCAGCTCCTTGAAAGG CTCTACAAAAAATAAGAACAGCCAGGCATGGTCGTGAGTGCCGGTAGTCCCAGCTCCTTGAAAGG T G AC023055.1,SARNP Ensembl:ENSG00000257390,Ensembl:ENSG00000205323 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1235994784 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36264,RMVar_hsa_circ_35258 33911 RMVar_ID_33911 Human_SNP_ID_502234967 A-to-I Human chr12 - 55782715 55782715 55782715 GTGCAGTGTGGCACATGCCTGTGGTCCCAGCTACTTAGGAGACTGAGGTGGGAGGATTGCTTGAG GTGCAGTGTGGCACATGCCTGTGGTCCCAGCTGCTTAGGAGACTGAGGTGGGAGGATTGCTTGAG T C AC023055.1,SARNP Ensembl:ENSG00000257390,Ensembl:ENSG00000205323 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs982803928 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17561146 RMVar_hsa_circ_36264,RMVar_hsa_circ_35258 33912 RMVar_ID_33912 Human_SNP_ID_502234980 A-to-I Human chr12 - 55782749 55782749 55782749 TGTCTTCTATAAAATGTAAAAACAAATTAGCCAGGTGCAGTGTGGCACATGCCTGTGGTCCCAGC TGTCTTCTATAAAATGTAAAAACAAATTAGCCCGGTGCAGTGTGGCACATGCCTGTGGTCCCAGC T G AC023055.1,SARNP Ensembl:ENSG00000257390,Ensembl:ENSG00000205323 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264965623 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36264,RMVar_hsa_circ_35258 33913 RMVar_ID_33913 Human_SNP_ID_502235043 A-to-I Human chr12 - 55783035 55783034 55783035 CGCAATGATAGCTCACTGCAGCCTCAGCCTCCAGGGTCAAGTGATCCTCCCACCTCAGCCTCCTG CGCAATGATAGCTCACTGCAGCCTCAGCCTCC_GGGTCAAGTGATCCTCCCACCTCAGCCTCCTG CT C AC023055.1,SARNP Ensembl:ENSG00000257390,Ensembl:ENSG00000205323 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs981259317 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_36264,RMVar_hsa_circ_35258 33914 RMVar_ID_33914 Human_SNP_ID_502235044 A-to-I Human chr12 - 55783035 55783035 55783035 CGCAATGATAGCTCACTGCAGCCTCAGCCTCCAGGGTCAAGTGATCCTCCCACCTCAGCCTCCTG CGCAATGATAGCTCACTGCAGCCTCAGCCTCCCGGGTCAAGTGATCCTCCCACCTCAGCCTCCTG T G AC023055.1,SARNP Ensembl:ENSG00000257390,Ensembl:ENSG00000205323 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1033729590 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36264,RMVar_hsa_circ_35258 33915 RMVar_ID_33915 Human_SNP_ID_502235923 A-to-I Human chr12 - 55786561 55786561 55786561 CCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAACTCGGAGGGCGGAGGCT CCTGTAATCCCAGCTACTTGGGAGGCTGAGGCTGGAGAATCGCTTGAACTCGGAGGGCGGAGGCT T A AC023055.1,SARNP Ensembl:ENSG00000257390,Ensembl:ENSG00000205323 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs948525283 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36264,RMVar_hsa_circ_35258 33916 RMVar_ID_33916 Human_SNP_ID_502236072 A-to-I Human chr12 - 55787137 55787137 55787137 GCCTCCATTTCCCAGGCTCAAGCAAGCCTCCCACCTCAGCCTCCTGAGTAGGTGGGACCACAGAT GCCTCCATTTCCCAGGCTCAAGCAAGCCTCCCCCCTCAGCCTCCTGAGTAGGTGGGACCACAGAT T G AC023055.1,SARNP Ensembl:ENSG00000257390,Ensembl:ENSG00000205323 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs909390221 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36264,RMVar_hsa_circ_35258 33917 RMVar_ID_33917 Human_SNP_ID_502236526 A-to-I Human chr12 - 55788677 55788677 55788677 CTCCCACCTCAGCCTTTCTCGTAGCTAAAACTACAGGCACGTGCCACCATGCCCAGCTAATTTTT CTCCCACCTCAGCCTTTCTCGTAGCTAAAACTGCAGGCACGTGCCACCATGCCCAGCTAATTTTT T C AC023055.1,SARNP Ensembl:ENSG00000257390,Ensembl:ENSG00000205323 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1010015117 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36264,RMVar_hsa_circ_35258 33918 RMVar_ID_33918 Human_SNP_ID_502236527 A-to-I Human chr12 - 55788683 55788683 55788683 GTGATCCTCCCACCTCAGCCTTTCTCGTAGCTAAAACTACAGGCACGTGCCACCATGCCCAGCTA GTGATCCTCCCACCTCAGCCTTTCTCGTAGCTGAAACTACAGGCACGTGCCACCATGCCCAGCTA T C AC023055.1,SARNP Ensembl:ENSG00000257390,Ensembl:ENSG00000205323 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs779571237 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36264,RMVar_hsa_circ_35258 33919 RMVar_ID_33919 Human_SNP_ID_502237630 A-to-I Human chr12 - 55793103 55793103 55793103 TAATTTTTGTATTATTAGTAGAGACAGGTTTCACTGTGTTGGCCAGGCTGGTCTTGAACTCCTAA TAATTTTTGTATTATTAGTAGAGACAGGTTTCCCTGTGTTGGCCAGGCTGGTCTTGAACTCCTAA T G AC023055.1,SARNP Ensembl:ENSG00000257390,Ensembl:ENSG00000205323 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs12824514 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36264,RMVar_hsa_circ_157120,RMVar_hsa_circ_35258,RMVar_hsa_circ_296409,RMVar_hsa_circ_343802,RMVar_hsa_circ_345304,RMVar_hsa_circ_315736,RMVar_hsa_circ_276457,RMVar_hsa_circ_157118,RMVar_hsa_circ_157119,RMVar_hsa_circ_157117 33920 RMVar_ID_33920 Human_SNP_ID_502239387 A-to-I Human chr12 - 55800024 55800024 55800024 ACTACTGCCCGACTGATTTTTGTATTTTTAGTAGAGACAGGGTTTTACCATGTTGGCCAGGCTGG ACTACTGCCCGACTGATTTTTGTATTTTTAGTGGAGACAGGGTTTTACCATGTTGGCCAGGCTGG T C AC023055.1,SARNP Ensembl:ENSG00000257390,Ensembl:ENSG00000205323 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1390212816 Functional Loss SNV dbSNP153 33..33 33 - - - 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_157122 33921 RMVar_ID_33921 Human_SNP_ID_502239389 A-to-I Human chr12 - 55800033 55800033 55800033 GTGTGTGCCACTACTGCCCGACTGATTTTTGTATTTTTAGTAGAGACAGGGTTTTACCATGTTGG GTGTGTGCCACTACTGCCCGACTGATTTTTGTGTTTTTAGTAGAGACAGGGTTTTACCATGTTGG T C AC023055.1,SARNP Ensembl:ENSG00000257390,Ensembl:ENSG00000205323 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs746944064 Functional Loss SNV dbSNP153 33..33 33 - - - 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_157122 33922 RMVar_ID_33922 Human_SNP_ID_502239676 A-to-I Human chr12 - 55801321 55801321 55801321 TTCCCACTTCAGCCTCCCCAGTAGCTAAGACTATAGGCGCACACCCCCACACCCAGCTAATTTTT TTCCCACTTCAGCCTCCCCAGTAGCTAAGACTTTAGGCGCACACCCCCACACCCAGCTAATTTTT T A AC023055.1,SARNP Ensembl:ENSG00000257390,Ensembl:ENSG00000205323 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1293303409 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_157120,RMVar_hsa_circ_35258,RMVar_hsa_circ_276457,RMVar_hsa_circ_157119,RMVar_hsa_circ_310136,RMVar_hsa_circ_127815,RMVar_hsa_circ_311987,RMVar_hsa_circ_275257,RMVar_hsa_circ_157122 33923 RMVar_ID_33923 Human_SNP_ID_502239752 A-to-I Human chr12 - 55801694 55801694 55801694 AGGATCCCTTGAGCCCAGGAGGGGGAGGCTGCAGGGAGCTGTGATTGTGCCATTGCACTTTATCT AGGATCCCTTGAGCCCAGGAGGGGGAGGCTGCGGGGAGCTGTGATTGTGCCATTGCACTTTATCT T C AC023055.1,SARNP Ensembl:ENSG00000257390,Ensembl:ENSG00000205323 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1212109035 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_157120,RMVar_hsa_circ_35258,RMVar_hsa_circ_276457,RMVar_hsa_circ_157119,RMVar_hsa_circ_310136,RMVar_hsa_circ_127815,RMVar_hsa_circ_311987,RMVar_hsa_circ_275257,RMVar_hsa_circ_157122 33924 RMVar_ID_33924 Human_SNP_ID_502239763 A-to-I Human chr12 - 55801734 55801734 55801734 GTGCACCTGTAGTCCTACCTACTTGGGAGGCTAAGGCAGGAGGATCCCTTGAGCCCAGGAGGGGG GTGCACCTGTAGTCCTACCTACTTGGGAGGCTGAGGCAGGAGGATCCCTTGAGCCCAGGAGGGGG T C AC023055.1,SARNP Ensembl:ENSG00000257390,Ensembl:ENSG00000205323 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1301389715 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24982645 RMVar_hsa_circ_157120,RMVar_hsa_circ_35258,RMVar_hsa_circ_276457,RMVar_hsa_circ_157119,RMVar_hsa_circ_310136,RMVar_hsa_circ_127815,RMVar_hsa_circ_311987,RMVar_hsa_circ_275257,RMVar_hsa_circ_157122 33925 RMVar_ID_33925 Human_SNP_ID_502240739 A-to-I Human chr12 - 55805590 55805590 55805590 TGCCTGCCTAGGCCCCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCACCTGGTCTAGTTTT TGCCTGCCTAGGCCCCCCAAAGTGCTGGGATTGCAGGCGTGAGCCACCGCACCTGGTCTAGTTTT T C AC023055.1,SARNP Ensembl:ENSG00000257390,Ensembl:ENSG00000205323 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1401184767 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_157120,RMVar_hsa_circ_127815,RMVar_hsa_circ_157122 33926 RMVar_ID_33926 Human_SNP_ID_502240845 A-to-I Human chr12 - 55805998 55805998 55805998 AATTTTGTTCTTGGCATCCAGGCTGGAGCGCAATGATGTGATCTCGGCTCACTGCAACCTCTGCG AATTTTGTTCTTGGCATCCAGGCTGGAGCGCAGTGATGTGATCTCGGCTCACTGCAACCTCTGCG T C AC023055.1,SARNP Ensembl:ENSG00000257390,Ensembl:ENSG00000205323 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs549717083 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11983233 RMVar_hsa_circ_157120,RMVar_hsa_circ_127815,RMVar_hsa_circ_157122 33927 RMVar_ID_33927 Human_SNP_ID_502241122 A-to-I Human chr12 - 55807019 55807019 55807019 GGAGGTTCGGGTGGGAGGATTTCTTGAGTTCAAGAGTTTAAGTTCAGCCCGGGCAACATGGCGAG GGAGGTTCGGGTGGGAGGATTTCTTGAGTTCAGGAGTTTAAGTTCAGCCCGGGCAACATGGCGAG T C AC023055.1,SARNP Ensembl:ENSG00000257390,Ensembl:ENSG00000205323 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1238816881 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_157120,RMVar_hsa_circ_127815,RMVar_hsa_circ_157122 33928 RMVar_ID_33928 Human_SNP_ID_502241222 A-to-I Human chr12 - 55807407 55807407 55807407 CCTTGGCCTCACAAGGGGCTGGAATTGTAAGCATAAGCCACCAAGATCAAGATTGTTACTTAATA CCTTGGCCTCACAAGGGGCTGGAATTGTAAGCGTAAGCCACCAAGATCAAGATTGTTACTTAATA T C AC023055.1,SARNP Ensembl:ENSG00000257390,Ensembl:ENSG00000205323 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7954839 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_157120,RMVar_hsa_circ_127815,RMVar_hsa_circ_157122 33929 RMVar_ID_33929 Human_SNP_ID_502242068 A-to-I Human chr12 - 55810350 55810350 55810350 CCAACACTTTGGGAGGCTGAGGCAGGAGGATCACTTGAGCCCAGGAGTTTAAGAACAGCCTGGGC CCAACACTTTGGGAGGCTGAGGCAGGAGGATCCCTTGAGCCCAGGAGTTTAAGAACAGCCTGGGC T G AC023055.1,SARNP Ensembl:ENSG00000257390,Ensembl:ENSG00000205323 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs886257798 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_157120,RMVar_hsa_circ_127815,RMVar_hsa_circ_157122 33930 RMVar_ID_33930 Human_SNP_ID_502243304 A-to-I Human chr12 - 55815087 55815087 55815087 AATTGCTCCACTGCACTTCAGCCTGGGTGACAAAGGGAGACCTTGTCTCAAAAAAAAGAAAATAA AATTGCTCCACTGCACTTCAGCCTGGGTGACAGAGGGAGACCTTGTCTCAAAAAAAAGAAAATAA T C AC023055.1,SARNP Ensembl:ENSG00000257390,Ensembl:ENSG00000205323 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1174340139 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_157120,RMVar_hsa_circ_127815,RMVar_hsa_circ_157122 33931 RMVar_ID_33931 Human_SNP_ID_502245838 A-to-I Human chr12 + 55823938 55823938 55823938 GTTGGCCAGTCTGGTCTCGAACTCCTGACCTCAAGAGATCTGCCTACCTCAGCCTCCCAAAGTGC GTTGGCCAGTCTGGTCTCGAACTCCTGACCTCCAGAGATCTGCCTACCTCAGCCTCCCAAAGTGC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1331355182 Functional Loss SNV dbSNP153 33..33 33 - - - 33932 RMVar_ID_33932 Human_SNP_ID_502246062 A-to-I Human chr12 - 55824965 55824965 55824965 ACCACACCTGGCTAATTTTTTGTATTTTTAGTAGAAATGGGGTTTTGTTATGTTGGCTAGCCTGA ACCACACCTGGCTAATTTTTTGTATTTTTAGTGGAAATGGGGTTTTGTTATGTTGGCTAGCCTGA T C AC023055.1,DNAJC14 Ensembl:ENSG00000257390,Ensembl:ENSG00000135392 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1221003292 Functional Loss SNV dbSNP153 33..33 33 - - - 33933 RMVar_ID_33933 Human_SNP_ID_502246178 A-to-I Human chr12 - 55825431 55825431 55825431 TAGAAGTAGATATTAGGTTGATATTAGATAACAGATTGTTACTGCTATTTCTGTACAAATAAAAC TAGAAGTAGATATTAGGTTGATATTAGATAACGGATTGTTACTGCTATTTCTGTACAAATAAAAC T C AC023055.1,DNAJC14 Ensembl:ENSG00000257390,Ensembl:ENSG00000135392 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7956337 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_3660 33934 RMVar_ID_33934 Human_SNP_ID_502246179 A-to-I Human chr12 - 55825431 55825431 55825431 TAGAAGTAGATATTAGGTTGATATTAGATAACAGATTGTTACTGCTATTTCTGTACAAATAAAAC TAGAAGTAGATATTAGGTTGATATTAGATAACCGATTGTTACTGCTATTTCTGTACAAATAAAAC T G AC023055.1,DNAJC14 Ensembl:ENSG00000257390,Ensembl:ENSG00000135392 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7956337 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_3660 33935 RMVar_ID_33935 Human_SNP_ID_502248618 A-to-I Human chr12 + 55833834 55833834 55833834 CGGGGGGGTGCTGGGCACGGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCCAAGGCGGGC CGGGGGGGTGCTGGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGC A G TMEM198B Ensembl:ENSG00000182796 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs372235974 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17357943 33936 RMVar_ID_33936 Human_SNP_ID_502248806 A-to-I Human chr12 + 55834368 55834368 55834368 TCACTGTAACCTCCGCCTCCTGGATTCAAGTGATTCTCATGCCTCAGCTTCCCGAGTAGCTGGGA TCACTGTAACCTCCGCCTCCTGGATTCAAGTGTTTCTCATGCCTCAGCTTCCCGAGTAGCTGGGA A T TMEM198B Ensembl:ENSG00000182796 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs986338935 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17357945 Human_Splice_Rec_1379506,Human_Splice_Rec_1379526 33937 RMVar_ID_33937 Human_SNP_ID_502248826 A-to-I Human chr12 + 55834464 55834464 55834464 TTTTGTATCTTTAGTAGAGATGGGGTTTCACCATGTTAGCCAGGCTGGTCTTGAACTCCCAACCT TTTTGTATCTTTAGTAGAGATGGGGTTTCACCGTGTTAGCCAGGCTGGTCTTGAACTCCCAACCT A G TMEM198B Ensembl:ENSG00000182796 Pseudogene intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1244837485 Functional Loss SNV dbSNP153 33..33 33 - - - 33938 RMVar_ID_33938 Human_SNP_ID_502267460 A-to-I Human chr12 - 55907526 55907526 55907526 TGTTTCAAGTGATTCTCCTGCTTCAACCTCCCAAGTAGCTGGGATTACAAGCGCATGCCGCCGTG TGTTTCAAGTGATTCTCCTGCTTCAACCTCCCGAGTAGCTGGGATTACAAGCGCATGCCGCCGTG T C PYM1 Ensembl:ENSG00000170473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1068189 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90586,RMVar_hsa_circ_95992,RMVar_hsa_circ_157125,RMVar_hsa_circ_157126 33939 RMVar_ID_33939 Human_SNP_ID_502267477 A-to-I Human chr12 - 55907587 55907587 55907587 GCTCTGTCACCAGGCTGGAGTGCAGTGGCTCAATCTCGGCTTACTGCAACCTCCAACCCCCTGTT GCTCTGTCACCAGGCTGGAGTGCAGTGGCTCAGTCTCGGCTTACTGCAACCTCCAACCCCCTGTT T C PYM1 Ensembl:ENSG00000170473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs965831273 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90586,RMVar_hsa_circ_95992,RMVar_hsa_circ_157125,RMVar_hsa_circ_157126 33940 RMVar_ID_33940 Human_SNP_ID_502268453 A-to-I Human chr12 - 55911273 55911273 55911273 ACCCCATCTCTACTTAAAAATATATAAAAATTAGCCGGACGTGGTGGCACACATCTGTAATCCCA ACCCCATCTCTACTTAAAAATATATAAAAATTGGCCGGACGTGGTGGCACACATCTGTAATCCCA T C PYM1 Ensembl:ENSG00000170473 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1275760240 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90586,RMVar_hsa_circ_95992,RMVar_hsa_circ_157125,RMVar_hsa_circ_157126 33941 RMVar_ID_33941 Human_SNP_ID_502268573 A-to-I Human chr12 - 55911758 55911758 55911758 CGGCTCATTGCAACCTCCCCCTCCTGGGATCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCT CGGCTCATTGCAACCTCCCCCTCCTGGGATCAGGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCT T C PYM1 Ensembl:ENSG00000170473 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1448909573 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90586,RMVar_hsa_circ_95992,RMVar_hsa_circ_157125,RMVar_hsa_circ_157126 33942 RMVar_ID_33942 Human_SNP_ID_502269755 A-to-I Human chr12 - 55916844 55916844 55916844 AGCCTCCCAAAGTGTTGGGATTAGAGGCATGAACCACCACGCCCAACCTCAGACTACTTTCTTTT AGCCTCCCAAAGTGTTGGGATTAGAGGCATGAGCCACCACGCCCAACCTCAGACTACTTTCTTTT T C PYM1 Ensembl:ENSG00000170473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1681070 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90586,RMVar_hsa_circ_95992,RMVar_hsa_circ_157125,RMVar_hsa_circ_157126 33943 RMVar_ID_33943 Human_SNP_ID_502269756 A-to-I Human chr12 - 55916844 55916844 55916844 AGCCTCCCAAAGTGTTGGGATTAGAGGCATGAACCACCACGCCCAACCTCAGACTACTTTCTTTT AGCCTCCCAAAGTGTTGGGATTAGAGGCATGACCCACCACGCCCAACCTCAGACTACTTTCTTTT T G PYM1 Ensembl:ENSG00000170473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1681070 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90586,RMVar_hsa_circ_95992,RMVar_hsa_circ_157125,RMVar_hsa_circ_157126 33944 RMVar_ID_33944 Human_SNP_ID_502270226 A-to-I Human chr12 - 55918821 55918821 55918821 CTCTGTCGCCCAGGCTGGAGTGCAGTGGTGCAATCTCGGCTCAGTGCGACCTCTGCCTCTCAGGT CTCTGTCGCCCAGGCTGGAGTGCAGTGGTGCAGTCTCGGCTCAGTGCGACCTCTGCCTCTCAGGT T C PYM1 Ensembl:ENSG00000170473 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs899710033 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90586,RMVar_hsa_circ_95992,RMVar_hsa_circ_157125,RMVar_hsa_circ_157126 33945 RMVar_ID_33945 Human_SNP_ID_502270340 A-to-I Human chr12 - 55919347 55919347 55919347 GAATTCGAGACCAGCCTGGGCAACATGGCAAAACCTCGTCTCTACTAAAAATACAAAAAATTAAC GAATTCGAGACCAGCCTGGGCAACATGGCAAATCCTCGTCTCTACTAAAAATACAAAAAATTAAC T A PYM1 Ensembl:ENSG00000170473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1273122169 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90586,RMVar_hsa_circ_95992,RMVar_hsa_circ_157125,RMVar_hsa_circ_157126 33946 RMVar_ID_33946 Human_SNP_ID_502270344 A-to-I Human chr12 - 55919377 55919377 55919377 GGCTGAGGCGGGTGGATTGCTTGAGCCCAGGAATTCGAGACCAGCCTGGGCAACATGGCAAAACC GGCTGAGGCGGGTGGATTGCTTGAGCCCAGGAGTTCGAGACCAGCCTGGGCAACATGGCAAAACC T C PYM1 Ensembl:ENSG00000170473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1254514852 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90586,RMVar_hsa_circ_95992,RMVar_hsa_circ_157125,RMVar_hsa_circ_157126 33947 RMVar_ID_33947 Human_SNP_ID_502270596 A-to-I Human chr12 - 55920455 55920455 55920455 TTTTGTATTTTTAGTAGAGATGGTGTTTTACCATGTTGTCTAGGCTGGTCTTGAACTCCTGGCCT TTTTGTATTTTTAGTAGAGATGGTGTTTTACCGTGTTGTCTAGGCTGGTCTTGAACTCCTGGCCT T C PYM1 Ensembl:ENSG00000170473 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215426258 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90586,RMVar_hsa_circ_95992,RMVar_hsa_circ_157125,RMVar_hsa_circ_157126 33948 RMVar_ID_33948 Human_SNP_ID_502276761 A-to-I Human chr12 + 55944161 55944161 55944161 CTACAAAATATTTTTTAAAAAATTAGCTGGGCATGGTGGCACGCACCTGTAGTCCCAACAACTCA CTACAAAATATTTTTTAAAAAATTAGCTGGGCGTGGTGGCACGCACCTGTAGTCCCAACAACTCA A G DGKA Ensembl:ENSG00000065357 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1009566459 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19053,RMVar_hsa_circ_28816,RMVar_hsa_circ_76165,RMVar_hsa_circ_157130 33949 RMVar_ID_33949 Human_SNP_ID_502277753 A-to-I Human chr12 + 55948581 55948580 55948581 GAGACCTCATCTCTATGAAAAATAAAATAATTAACCAGGCATGGTGGCACACGCTTGTGGTTCCA GAGACCTCATCTCTATGAAAAATAAAATAATT_ACCAGGCATGGTGGCACACGCTTGTGGTTCCA TA T DGKA Ensembl:ENSG00000065357 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270573747 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_19053,RMVar_hsa_circ_28816,RMVar_hsa_circ_76165,RMVar_hsa_circ_157130 33950 RMVar_ID_33950 Human_SNP_ID_502286065 A-to-I Human chr12 - 55980701 55980701 55980701 AACTGGATGAAAAGCATCATGGAGAATGCCTCAGCTGGGGTGGAGCACCTCTTGCTAGGGAACAA AACTGGATGAAAAGCATCATGGAGAATGCCTCGGCTGGGGTGGAGCACCTCTTGCTAGGGAACAA T C AC034102.1 Ensembl:ENSG00000237493 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878918968 Functional Loss SNV dbSNP153 33..33 33 - - - 33951 RMVar_ID_33951 Human_SNP_ID_502287395 A-to-I Human chr12 + 55986286 55986286 55986286 TCTGACCAACATGGAGAAACTCCGTCTCTACTAAAAATACAAAATTAGCCAGGCGTGGTGGTGCA TCTGACCAACATGGAGAAACTCCGTCTCTACTGAAAATACAAAATTAGCCAGGCGTGGTGGTGCA A G RAB5B Ensembl:ENSG00000111540 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1442097086 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5938 33952 RMVar_ID_33952 Human_SNP_ID_502287551 A-to-I Human chr12 - 55986905 55986904 55986905 GGGTGGAGGGAGGGGGATACTGTAAAGGGGGGAGGGGGAAGGGGAGGGGATTTCCAGGCTTCAAC GGGTGGAGGGAGGGGGATACTGTAAAGGGGGG_GGGGGAAGGGGAGGGGATTTCCAGGCTTCAAC CT C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs756350502 Functional Loss DEL dbSNP153 33..33 33 - - - 33953 RMVar_ID_33953 Human_SNP_ID_502287552 A-to-I Human chr12 - 55986905 55986905 55986905 GGGTGGAGGGAGGGGGATACTGTAAAGGGGGGAGGGGGAAGGGGAGGGGATTTCCAGGCTTCAAC GGGTGGAGGGAGGGGGATACTGTAAAGGGGGGGGGGGGAAGGGGAGGGGATTTCCAGGCTTCAAC T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs370178643 Functional Loss SNV dbSNP153 33..33 33 - - - 33954 RMVar_ID_33954 Human_SNP_ID_502314863 A-to-I Human chr12 + 56090374 56090374 56090374 CCACATATGGCCGGGCACAGTGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCTGAGGCAGGT CCACATATGGCCGGGCACAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGT A G ERBB3 Ensembl:ENSG00000065361 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1018807980 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17561158 RMVar_hsa_circ_78618,RMVar_hsa_circ_157144,RMVar_hsa_circ_54446,RMVar_hsa_circ_108879,RMVar_hsa_circ_157147,RMVar_hsa_circ_111621,RMVar_hsa_circ_157150,RMVar_hsa_circ_127409,RMVar_hsa_circ_157151 33955 RMVar_ID_33955 Human_SNP_ID_502327988 A-to-I Human chr12 + 56135518 56135518 56135518 TTAAAGGTCATAGAAAAAGCACAAAACATAGTATCTGCCTTCACAATACTCACTGGCCAGTTTCA TTAAAGGTCATAGAAAAAGCACAAAACATAGTGTCTGCCTTCACAATACTCACTGGCCAGTTTCA A G ESYT1 Ensembl:ENSG00000139641 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs115391641 Functional Loss SNV dbSNP153 33..33 33 - - - 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_109407,RMVar_hsa_circ_157188,RMVar_hsa_circ_157190,RMVar_hsa_circ_157191,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_157199,RMVar_hsa_circ_157201,RMVar_hsa_circ_80348,RMVar_hsa_circ_157200 33956 RMVar_ID_33956 Human_SNP_ID_502331116 A-to-I Human chr12 + 56145837 56145837 56145837 AAAATTAGCTGGGCGTGGTGGTGGACGCCTGTAGTCCCAGCTACTCGGGAGGCTGAAACAGGAGA AAAATTAGCTGGGCGTGGTGGTGGACGCCTGTGGTCCCAGCTACTCGGGAGGCTGAAACAGGAGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs890453592 Functional Loss SNV dbSNP153 33..33 33 - - - 33957 RMVar_ID_33957 Human_SNP_ID_502333688 A-to-I Human chr12 + 56155053 56155052 56155054 TCAGTGTCTACACTGACCCTTCCTTATACTTTAGAGTTCAAGGAGGCCTTCGAGCTGTTTGACCG TCAGTGTCTACACTGACCCTTCCTTATACTTT__AGTTCAAGGAGGCCTTCGAGCTGTTTGACCG TAG T MYL6B Ensembl:ENSG00000196465 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1418382984 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_18189163 RMVar_hsa_circ_104306,RMVar_hsa_circ_101581,RMVar_hsa_circ_111642,RMVar_hsa_circ_157220,RMVar_hsa_circ_157221 33958 RMVar_ID_33958 Human_SNP_ID_502335487 A-to-I Human chr12 + 56160151 56160151 56160151 CTGAAATCCGGCATGTTCTTGTCACACTGGGTAAGGTTCTGTGTCCTTGTCCTTGAGCTGAGATG CTGAAATCCGGCATGTTCTTGTCACACTGGGTGAGGTTCTGTGTCCTTGTCCTTGAGCTGAGATG A G MYL6 Ensembl:ENSG00000092841 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879033700 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19058362,Human_RBP_ID_22436507 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_157236 33959 RMVar_ID_33959 Human_SNP_ID_502337455 A-to-I Human chr12 - 56166714 56166706 56166715 GTGGTGGTGCGAGCCTGTGGTCCCAGCTACTCAGGAAGCTGAGGTGGGAGGATCGTTTGAGCCCA GTGGTGGTGCGAGCCTGTGGTCCCAGCTACT_________GAGGTGGGAGGATCGTTTGAGCCCA CAGCTTCCTG C AC073896.4,SMARCC2 Ensembl:ENSG00000258199,Ensembl:ENSG00000139613 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1255007020 Functional Loss DEL dbSNP153 32..40 33 - - - Human_RBP_ID_5246404 RMVar_hsa_circ_35361 33960 RMVar_ID_33960 Human_SNP_ID_502338048 A-to-I Human chr12 - 56168453 56168453 56168453 CGAGAATTGCTTGAACCCAGGAGGTAGAGGTTACAGTGAGCTGAGATCATGCCACTGTACTCCAG CGAGAATTGCTTGAACCCAGGAGGTAGAGGTTGCAGTGAGCTGAGATCATGCCACTGTACTCCAG T C AC073896.4,SMARCC2 Ensembl:ENSG00000258199,Ensembl:ENSG00000139613 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1198978492 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35361,RMVar_hsa_circ_341984,RMVar_hsa_circ_359882 33961 RMVar_ID_33961 Human_SNP_ID_502338050 A-to-I Human chr12 - 56168460 56168460 56168460 AAAGGCACGAGAATTGCTTGAACCCAGGAGGTAGAGGTTACAGTGAGCTGAGATCATGCCACTGT AAAGGCACGAGAATTGCTTGAACCCAGGAGGTTGAGGTTACAGTGAGCTGAGATCATGCCACTGT T A AC073896.4,SMARCC2 Ensembl:ENSG00000258199,Ensembl:ENSG00000139613 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1271582847 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35361,RMVar_hsa_circ_341984,RMVar_hsa_circ_359882 33962 RMVar_ID_33962 Human_SNP_ID_502338136 A-to-I Human chr12 - 56168814 56168814 56168814 CAGCATGCCCGGTTAATTTTTGTATTTTTAGCAGAGATGGGGTTTCACCCTGTTGCCCCAGGCTG CAGCATGCCCGGTTAATTTTTGTATTTTTAGCGGAGATGGGGTTTCACCCTGTTGCCCCAGGCTG T C AC073896.4,SMARCC2 Ensembl:ENSG00000258199,Ensembl:ENSG00000139613 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1230741354 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35361,RMVar_hsa_circ_341984,RMVar_hsa_circ_359882 33963 RMVar_ID_33963 Human_SNP_ID_502338139 A-to-I Human chr12 - 56168823 56168823 56168823 GGCACGTGCCAGCATGCCCGGTTAATTTTTGTATTTTTAGCAGAGATGGGGTTTCACCCTGTTGC GGCACGTGCCAGCATGCCCGGTTAATTTTTGTGTTTTTAGCAGAGATGGGGTTTCACCCTGTTGC T C AC073896.4,SMARCC2 Ensembl:ENSG00000258199,Ensembl:ENSG00000139613 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs879347472 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35361,RMVar_hsa_circ_341984,RMVar_hsa_circ_359882 33964 RMVar_ID_33964 Human_SNP_ID_502347639 A-to-I Human chr12 - 56203722 56203722 56203722 CAGCCTGGGCGACAGAGCAAGGCTCCGTCTAAAAAAAAAAAAAAAAAAAAAAGTCTTCATAGGCC CAGCCTGGGCGACAGAGCAAGGCTCCGTCTAACAAAAAAAAAAAAAAAAAAAGTCTTCATAGGCC T G RNF41 Ensembl:ENSG00000181852 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs75288681 Functional Loss SNV dbSNP153 33..33 33 - - - 33965 RMVar_ID_33965 Human_SNP_ID_502351230 A-to-I Human chr12 - 56218227 56218227 56218227 TATGTGGGCCAGGCGCGGTGGCTCACACTTGTAATCCCAGCATTTTGGGAGGCTGAGGCGGGTGG TATGTGGGCCAGGCGCGGTGGCTCACACTTGTGATCCCAGCATTTTGGGAGGCTGAGGCGGGTGG T C RNF41 Ensembl:ENSG00000181852 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1252030453 Functional Loss SNV dbSNP153 33..33 33 - - - 33966 RMVar_ID_33966 Human_SNP_ID_502351797 A-to-I Human chr12 - 56220155 56220155 56220155 GTGATTGGTCCATCTCGGCTTCCCAAAGTGCTAGGATTACAGGCATGAGCCACTGCACCCAGCCT GTGATTGGTCCATCTCGGCTTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGCACCCAGCCT T C RNF41 Ensembl:ENSG00000181852 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1197394850 Functional Loss SNV dbSNP153 33..33 33 - - - 33967 RMVar_ID_33967 Human_SNP_ID_502351905 A-to-I Human chr12 - 56220585 56220585 56220585 GGATTACAGGTACCTGCCACCATGCCTGGCTAATTTTTTGTATTTTTAGTTGAGATGGGGTTTCA GGATTACAGGTACCTGCCACCATGCCTGGCTAGTTTTTTGTATTTTTAGTTGAGATGGGGTTTCA T C RNF41 Ensembl:ENSG00000181852 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1415179818 Functional Loss SNV dbSNP153 33..33 33 - - - 33968 RMVar_ID_33968 Human_SNP_ID_502353680 A-to-I Human chr12 + 56227103 56227103 56227103 GATATGGTTTAAGAACTAGACTGGCTGGGCGCAGTGGCTCATGCCTATAATCTCAGCACTTTGGG GATATGGTTTAAGAACTAGACTGGCTGGGCGCGGTGGCTCATGCCTATAATCTCAGCACTTTGGG A G NABP2 Ensembl:ENSG00000139579 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs980977505 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89622,RMVar_hsa_circ_157267 33969 RMVar_ID_33969 Human_SNP_ID_502353681 A-to-I Human chr12 + 56227103 56227103 56227103 GATATGGTTTAAGAACTAGACTGGCTGGGCGCAGTGGCTCATGCCTATAATCTCAGCACTTTGGG GATATGGTTTAAGAACTAGACTGGCTGGGCGCTGTGGCTCATGCCTATAATCTCAGCACTTTGGG A T NABP2 Ensembl:ENSG00000139579 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs980977505 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89622,RMVar_hsa_circ_157267 33970 RMVar_ID_33970 Human_SNP_ID_502353684 A-to-I Human chr12 + 56227117 56227117 56227117 ACTAGACTGGCTGGGCGCAGTGGCTCATGCCTATAATCTCAGCACTTTGGGAGGCCAAGGCTGGC ACTAGACTGGCTGGGCGCAGTGGCTCATGCCTGTAATCTCAGCACTTTGGGAGGCCAAGGCTGGC A G NABP2 Ensembl:ENSG00000139579 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs926930973 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89622,RMVar_hsa_circ_157267 33971 RMVar_ID_33971 Human_SNP_ID_502354096 A-to-I Human chr12 + 56228651 56228651 56228651 CTCGTGATCCACCCGCGTCAGCCTCCCACCGTACTGAGATTACAGGTGTGAGCCACCACGCCTGG CTCGTGATCCACCCGCGTCAGCCTCCCACCGTTCTGAGATTACAGGTGTGAGCCACCACGCCTGG A T NABP2 Ensembl:ENSG00000139579 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs760068771 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89622,RMVar_hsa_circ_157267 33972 RMVar_ID_33972 Human_SNP_ID_502354391 A-to-I Human chr12 + 56229685 56229685 56229685 GAAACCGGGAGGCGGAGGTTGAGGTGAGCCGAAATTGCACCATTGCACTCCAGCCTGGGCAATAA GAAACCGGGAGGCGGAGGTTGAGGTGAGCCGAGATTGCACCATTGCACTCCAGCCTGGGCAATAA A G NABP2 Ensembl:ENSG00000139579 Protein coding 3'UTR GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1142868 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_423817 Human_miRNA_ID_2019650,Human_miRNA_ID_2024745,Human_miRNA_ID_2311363,Human_miRNA_ID_2313381,Human_miRNA_ID_2499476,Human_miRNA_ID_2607259,Human_miRNA_ID_2655166 RMVar_hsa_circ_89622,RMVar_hsa_circ_101629,RMVar_hsa_circ_157267,RMVar_hsa_circ_157268 33973 RMVar_ID_33973 Human_SNP_ID_502357470 A-to-I Human chr12 - 56239764 56239764 56239764 ACCTTCTTACTCCCTGGACCTAGAAGGGGAGAAGAGGCTGGAGGTGGGGTGGATGGGGCCAGAGT ACCTTCTTACTCCCTGGACCTAGAAGGGGAGAGGAGGCTGGAGGTGGGGTGGATGGGGCCAGAGT T C ANKRD52 Ensembl:ENSG00000139645 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 29129909,30559470 RNA-Seq:(High) rs929290293 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_753878,Human_RBP_ID_4232373,Human_RBP_ID_17243235,Human_RBP_ID_17357154 Human_miRNA_ID_2016269,Human_miRNA_ID_2974051,Human_miRNA_ID_3007239 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 33974 RMVar_ID_33974 Human_SNP_ID_502359179 A-to-I Human chr12 - 56246297 56246297 56246297 GGCCGGGCATGGTGGCTCACGTCTGTAATCCCAGCACTTTGGAAGGCCAAGGCGGGCAGATCACC GGCCGGGCATGGTGGCTCACGTCTGTAATCCCTGCACTTTGGAAGGCCAAGGCGGGCAGATCACC T A ANKRD52 Ensembl:ENSG00000139645 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1041397517 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106953,RMVar_hsa_circ_126467,RMVar_hsa_circ_111834,RMVar_hsa_circ_157275,RMVar_hsa_circ_97729,RMVar_hsa_circ_157277,RMVar_hsa_circ_80650,RMVar_hsa_circ_157278,RMVar_hsa_circ_157276,RMVar_hsa_circ_157274,RMVar_hsa_circ_83286,RMVar_hsa_circ_99260,RMVar_hsa_circ_157280,RMVar_hsa_circ_93719,RMVar_hsa_circ_106018,RMVar_hsa_circ_157281,RMVar_hsa_circ_157282,RMVar_hsa_circ_121949,RMVar_hsa_circ_265719,RMVar_hsa_circ_157283,RMVar_hsa_circ_157284,RMVar_hsa_circ_126415,RMVar_hsa_circ_157286,RMVar_hsa_circ_107425,RMVar_hsa_circ_157287 33975 RMVar_ID_33975 Human_SNP_ID_502360321 A-to-I Human chr12 - 56250346 56250346 56250346 AAAAAAAAAACCCACAAAAATCAGGTAGGCACAGTGACTCATGCCTGTAATTCCAGCACTGAGGT AAAAAAAAAACCCACAAAAATCAGGTAGGCACCGTGACTCATGCCTGTAATTCCAGCACTGAGGT T G ANKRD52 Ensembl:ENSG00000139645 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1193523076 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11986556,Human_RBP_ID_22493592 RMVar_hsa_circ_106953,RMVar_hsa_circ_126467,RMVar_hsa_circ_111834,RMVar_hsa_circ_157275,RMVar_hsa_circ_97729,RMVar_hsa_circ_157277,RMVar_hsa_circ_80650,RMVar_hsa_circ_157278,RMVar_hsa_circ_157276,RMVar_hsa_circ_157274,RMVar_hsa_circ_83286,RMVar_hsa_circ_99260,RMVar_hsa_circ_157280,RMVar_hsa_circ_93719,RMVar_hsa_circ_106018,RMVar_hsa_circ_157281,RMVar_hsa_circ_157282,RMVar_hsa_circ_121949,RMVar_hsa_circ_265719,RMVar_hsa_circ_157283,RMVar_hsa_circ_157284,RMVar_hsa_circ_126415,RMVar_hsa_circ_118106,RMVar_hsa_circ_102964,RMVar_hsa_circ_157286,RMVar_hsa_circ_107425,RMVar_hsa_circ_157287,RMVar_hsa_circ_157288,RMVar_hsa_circ_120013,RMVar_hsa_circ_116686,RMVar_hsa_circ_110249,RMVar_hsa_circ_93240,RMVar_hsa_circ_126631,RMVar_hsa_circ_157291,RMVar_hsa_circ_157292,RMVar_hsa_circ_157293,RMVar_hsa_circ_157290,RMVar_hsa_circ_112128,RMVar_hsa_circ_157294,RMVar_hsa_circ_107413,RMVar_hsa_circ_124554,RMVar_hsa_circ_97124,RMVar_hsa_circ_157296,RMVar_hsa_circ_157298,RMVar_hsa_circ_157300,RMVar_hsa_circ_87181,RMVar_hsa_circ_157299,RMVar_hsa_circ_157297,RMVar_hsa_circ_157295,RMVar_hsa_circ_104582,RMVar_hsa_circ_157302 33976 RMVar_ID_33976 Human_SNP_ID_502360387 A-to-I Human chr12 - 56250627 56250627 56250627 CTCCTGCCTCAGACTCCCAAAGTGCTGGGATTACAGATATGAGCCACCACACCTAGCCCACAATT CTCCTGCCTCAGACTCCCAAAGTGCTGGGATTGCAGATATGAGCCACCACACCTAGCCCACAATT T C ANKRD52 Ensembl:ENSG00000139645 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1482835584 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23158391,Human_RBP_ID_24983804 RMVar_hsa_circ_106953,RMVar_hsa_circ_126467,RMVar_hsa_circ_111834,RMVar_hsa_circ_157275,RMVar_hsa_circ_97729,RMVar_hsa_circ_157277,RMVar_hsa_circ_80650,RMVar_hsa_circ_157278,RMVar_hsa_circ_157276,RMVar_hsa_circ_157274,RMVar_hsa_circ_83286,RMVar_hsa_circ_99260,RMVar_hsa_circ_157280,RMVar_hsa_circ_93719,RMVar_hsa_circ_106018,RMVar_hsa_circ_157281,RMVar_hsa_circ_157282,RMVar_hsa_circ_121949,RMVar_hsa_circ_265719,RMVar_hsa_circ_157283,RMVar_hsa_circ_157284,RMVar_hsa_circ_126415,RMVar_hsa_circ_118106,RMVar_hsa_circ_102964,RMVar_hsa_circ_157286,RMVar_hsa_circ_107425,RMVar_hsa_circ_157287,RMVar_hsa_circ_157288,RMVar_hsa_circ_120013,RMVar_hsa_circ_116686,RMVar_hsa_circ_110249,RMVar_hsa_circ_93240,RMVar_hsa_circ_126631,RMVar_hsa_circ_157291,RMVar_hsa_circ_157292,RMVar_hsa_circ_157293,RMVar_hsa_circ_157290,RMVar_hsa_circ_112128,RMVar_hsa_circ_157294,RMVar_hsa_circ_107413,RMVar_hsa_circ_124554,RMVar_hsa_circ_97124,RMVar_hsa_circ_157296,RMVar_hsa_circ_157298,RMVar_hsa_circ_157300,RMVar_hsa_circ_87181,RMVar_hsa_circ_157299,RMVar_hsa_circ_157297,RMVar_hsa_circ_157295,RMVar_hsa_circ_104582,RMVar_hsa_circ_157302 33977 RMVar_ID_33977 Human_SNP_ID_502367472 A-to-I Human chr12 - 56277830 56277830 56277830 GAGGTCGGGAGTTCAAGACTAACCTGACCAACATGGTGAAACCCCCCTCTACTAAAAATACAAAA GAGGTCGGGAGTTCAAGACTAACCTGACCAACCTGGTGAAACCCCCCTCTACTAAAAATACAAAA T G CS Ensembl:ENSG00000062485 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs949055827 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117890,RMVar_hsa_circ_122808,RMVar_hsa_circ_108450,RMVar_hsa_circ_24586,RMVar_hsa_circ_157322,RMVar_hsa_circ_157324,RMVar_hsa_circ_157323,RMVar_hsa_circ_82371,RMVar_hsa_circ_157325,RMVar_hsa_circ_8991,RMVar_hsa_circ_323380,RMVar_hsa_circ_83353,RMVar_hsa_circ_106144,RMVar_hsa_circ_157327,RMVar_hsa_circ_295233,RMVar_hsa_circ_99303,RMVar_hsa_circ_29598,RMVar_hsa_circ_157329,RMVar_hsa_circ_157331,RMVar_hsa_circ_10990,RMVar_hsa_circ_157330,RMVar_hsa_circ_157328 33978 RMVar_ID_33978 Human_SNP_ID_502367623 A-to-I Human chr12 - 56278409 56278409 56278409 TAAAAAGTGACATGGGCTGGGTGCAGTGGCTCACGCCTGTAATCTCAGCACTTTGGGAGGCCGAG TAAAAAGTGACATGGGCTGGGTGCAGTGGCTCGCGCCTGTAATCTCAGCACTTTGGGAGGCCGAG T C CS Ensembl:ENSG00000062485 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1250076707 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117890,RMVar_hsa_circ_122808,RMVar_hsa_circ_108450,RMVar_hsa_circ_24586,RMVar_hsa_circ_157322,RMVar_hsa_circ_157324,RMVar_hsa_circ_157323,RMVar_hsa_circ_82371,RMVar_hsa_circ_157325,RMVar_hsa_circ_8991,RMVar_hsa_circ_323380,RMVar_hsa_circ_83353,RMVar_hsa_circ_106144,RMVar_hsa_circ_157327,RMVar_hsa_circ_295233,RMVar_hsa_circ_99303,RMVar_hsa_circ_29598,RMVar_hsa_circ_157329,RMVar_hsa_circ_157331,RMVar_hsa_circ_10990,RMVar_hsa_circ_157330,RMVar_hsa_circ_157328 33979 RMVar_ID_33979 Human_SNP_ID_502367681 A-to-I Human chr12 - 56278571 56278571 56278571 CACCACGCCCATCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTTGCCTTGTTGGCCAGGATGG CACCACGCCCATCTAATTTTTGTATTTTTAGTGGAGATGGGGTTTTGCCTTGTTGGCCAGGATGG T C CS Ensembl:ENSG00000062485 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1432221004 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117890,RMVar_hsa_circ_122808,RMVar_hsa_circ_108450,RMVar_hsa_circ_24586,RMVar_hsa_circ_157322,RMVar_hsa_circ_157324,RMVar_hsa_circ_157323,RMVar_hsa_circ_82371,RMVar_hsa_circ_157325,RMVar_hsa_circ_8991,RMVar_hsa_circ_323380,RMVar_hsa_circ_83353,RMVar_hsa_circ_106144,RMVar_hsa_circ_157327,RMVar_hsa_circ_295233,RMVar_hsa_circ_99303,RMVar_hsa_circ_29598,RMVar_hsa_circ_157329,RMVar_hsa_circ_157331,RMVar_hsa_circ_10990,RMVar_hsa_circ_157330,RMVar_hsa_circ_157328 33980 RMVar_ID_33980 Human_SNP_ID_502367684 A-to-I Human chr12 - 56278588 56278588 56278588 GGACCACAGGTGCAAGCCACCACGCCCATCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTTGC GGACCACAGGTGCAAGCCACCACGCCCATCTAGTTTTTGTATTTTTAGTAGAGATGGGGTTTTGC T C CS Ensembl:ENSG00000062485 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1014972004 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117890,RMVar_hsa_circ_122808,RMVar_hsa_circ_108450,RMVar_hsa_circ_24586,RMVar_hsa_circ_157322,RMVar_hsa_circ_157324,RMVar_hsa_circ_157323,RMVar_hsa_circ_82371,RMVar_hsa_circ_157325,RMVar_hsa_circ_8991,RMVar_hsa_circ_323380,RMVar_hsa_circ_83353,RMVar_hsa_circ_106144,RMVar_hsa_circ_157327,RMVar_hsa_circ_295233,RMVar_hsa_circ_99303,RMVar_hsa_circ_29598,RMVar_hsa_circ_157329,RMVar_hsa_circ_157331,RMVar_hsa_circ_10990,RMVar_hsa_circ_157330,RMVar_hsa_circ_157328 33981 RMVar_ID_33981 Human_SNP_ID_502367693 A-to-I Human chr12 - 56278613 56278613 56278613 CCTGCCTTGGCCTCCCGAGTAGCTGGGACCACAGGTGCAAGCCACCACGCCCATCTAATTTTTGT CCTGCCTTGGCCTCCCGAGTAGCTGGGACCACTGGTGCAAGCCACCACGCCCATCTAATTTTTGT T A CS Ensembl:ENSG00000062485 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1565619984 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23158406 RMVar_hsa_circ_117890,RMVar_hsa_circ_122808,RMVar_hsa_circ_108450,RMVar_hsa_circ_24586,RMVar_hsa_circ_157322,RMVar_hsa_circ_157324,RMVar_hsa_circ_157323,RMVar_hsa_circ_82371,RMVar_hsa_circ_157325,RMVar_hsa_circ_8991,RMVar_hsa_circ_323380,RMVar_hsa_circ_83353,RMVar_hsa_circ_106144,RMVar_hsa_circ_157327,RMVar_hsa_circ_295233,RMVar_hsa_circ_99303,RMVar_hsa_circ_29598,RMVar_hsa_circ_157329,RMVar_hsa_circ_157331,RMVar_hsa_circ_10990,RMVar_hsa_circ_157330,RMVar_hsa_circ_157328 33982 RMVar_ID_33982 Human_SNP_ID_502367731 A-to-I Human chr12 - 56278727 56278726 56278728 ATTTACCAACTTTTTTTTTTTTTTTCCGAGACAGAGTCTCTGTCGCTCAGGCTGCAGTGCAGTGG ATTTACCAACTTTTTTTTTTTTTTTCCGAGA__GAGTCTCTGTCGCTCAGGCTGCAGTGCAGTGG CTG C CS Ensembl:ENSG00000062485 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs977008848 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_11986861,Human_RBP_ID_17561160 RMVar_hsa_circ_117890,RMVar_hsa_circ_122808,RMVar_hsa_circ_108450,RMVar_hsa_circ_24586,RMVar_hsa_circ_157322,RMVar_hsa_circ_157324,RMVar_hsa_circ_157323,RMVar_hsa_circ_82371,RMVar_hsa_circ_157325,RMVar_hsa_circ_8991,RMVar_hsa_circ_323380,RMVar_hsa_circ_83353,RMVar_hsa_circ_106144,RMVar_hsa_circ_157327,RMVar_hsa_circ_295233,RMVar_hsa_circ_99303,RMVar_hsa_circ_29598,RMVar_hsa_circ_157329,RMVar_hsa_circ_157331,RMVar_hsa_circ_10990,RMVar_hsa_circ_157330,RMVar_hsa_circ_157328 33983 RMVar_ID_33983 Human_SNP_ID_502367773 A-to-I Human chr12 - 56278898 56278898 56278898 GTCCTGGTGCACACCTGTAATCCCAACTACTCAGGAGGCCGAGGTGGGAGAATCGCTTGAACCTA GTCCTGGTGCACACCTGTAATCCCAACTACTCGGGAGGCCGAGGTGGGAGAATCGCTTGAACCTA T C CS Ensembl:ENSG00000062485 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs71459355 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117890,RMVar_hsa_circ_122808,RMVar_hsa_circ_108450,RMVar_hsa_circ_24586,RMVar_hsa_circ_157322,RMVar_hsa_circ_157324,RMVar_hsa_circ_157323,RMVar_hsa_circ_82371,RMVar_hsa_circ_157325,RMVar_hsa_circ_8991,RMVar_hsa_circ_323380,RMVar_hsa_circ_83353,RMVar_hsa_circ_106144,RMVar_hsa_circ_157327,RMVar_hsa_circ_295233,RMVar_hsa_circ_99303,RMVar_hsa_circ_29598,RMVar_hsa_circ_157329,RMVar_hsa_circ_157331,RMVar_hsa_circ_10990,RMVar_hsa_circ_157330,RMVar_hsa_circ_157328 33984 RMVar_ID_33984 Human_SNP_ID_502367776 A-to-I Human chr12 - 56278912 56278905 56278936 AAAATTAGCTGAGCGTCCTGGTGCACACCTGTAATCCCAACTACTCAGGAGGCCGAGGTGGGAGA AAAATTAGATGGGCGTGGTGGCTTGCACCTGTGGTCCCAGCTACTCAGGAGGCCGAGGTGGGAGA TTGGGATTACAGGTGTGCACCAGGACGCTCAG CTGGGACCACAGGTGCAAGCCACCACGCCCAT CS Ensembl:ENSG00000062485 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs71457814 Functional Loss MNV dbSNP153 9..40 33 - - - RMVar_hsa_circ_117890,RMVar_hsa_circ_122808,RMVar_hsa_circ_108450,RMVar_hsa_circ_24586,RMVar_hsa_circ_157322,RMVar_hsa_circ_157324,RMVar_hsa_circ_157323,RMVar_hsa_circ_82371,RMVar_hsa_circ_157325,RMVar_hsa_circ_8991,RMVar_hsa_circ_323380,RMVar_hsa_circ_83353,RMVar_hsa_circ_106144,RMVar_hsa_circ_157327,RMVar_hsa_circ_295233,RMVar_hsa_circ_99303,RMVar_hsa_circ_29598,RMVar_hsa_circ_157329,RMVar_hsa_circ_157331,RMVar_hsa_circ_10990,RMVar_hsa_circ_157330,RMVar_hsa_circ_157328 33985 RMVar_ID_33985 Human_SNP_ID_502367950 A-to-I Human chr12 - 56279577 56279577 56279577 TATTTTTAGTAGAGTCGGGGTTTCACCGTGTTAGCCAGGATTGTCTCGATCTCCTGACCTCGTGA TATTTTTAGTAGAGTCGGGGTTTCACCGTGTTGGCCAGGATTGTCTCGATCTCCTGACCTCGTGA T C CS Ensembl:ENSG00000062485 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1372253000 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117890,RMVar_hsa_circ_122808,RMVar_hsa_circ_108450,RMVar_hsa_circ_24586,RMVar_hsa_circ_157322,RMVar_hsa_circ_157324,RMVar_hsa_circ_157323,RMVar_hsa_circ_82371,RMVar_hsa_circ_157325,RMVar_hsa_circ_8991,RMVar_hsa_circ_323380,RMVar_hsa_circ_83353,RMVar_hsa_circ_106144,RMVar_hsa_circ_157327,RMVar_hsa_circ_295233,RMVar_hsa_circ_99303,RMVar_hsa_circ_29598,RMVar_hsa_circ_157329,RMVar_hsa_circ_157331,RMVar_hsa_circ_10990,RMVar_hsa_circ_157330,RMVar_hsa_circ_157328 33986 RMVar_ID_33986 Human_SNP_ID_502369287 A-to-I Human chr12 - 56284485 56284485 56284485 GATCACCTGAGCCTGCAAGTCAAGGCTGCAGTAAGCCGTGATTGTGCCACTGTGCTGCAGCCTGA GATCACCTGAGCCTGCAAGTCAAGGCTGCAGTGAGCCGTGATTGTGCCACTGTGCTGCAGCCTGA T C CS Ensembl:ENSG00000062485 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1428730458 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11986969,Human_RBP_ID_17561708 RMVar_hsa_circ_117890,RMVar_hsa_circ_157324,RMVar_hsa_circ_82371,RMVar_hsa_circ_157325,RMVar_hsa_circ_8991,RMVar_hsa_circ_83353,RMVar_hsa_circ_106144,RMVar_hsa_circ_92622,RMVar_hsa_circ_157329,RMVar_hsa_circ_10990,RMVar_hsa_circ_157328,RMVar_hsa_circ_277144,RMVar_hsa_circ_27216,RMVar_hsa_circ_157334,RMVar_hsa_circ_157335,RMVar_hsa_circ_365232,RMVar_hsa_circ_331502 33987 RMVar_ID_33987 Human_SNP_ID_502369575 A-to-I Human chr12 - 56285563 56285563 56285563 GAATCAAACAGAGGGCGCAATGGCTCATGCCTATTATCCCAACATTTTGGGAGGCTGCAGTTGGA GAATCAAACAGAGGGCGCAATGGCTCATGCCTGTTATCCCAACATTTTGGGAGGCTGCAGTTGGA T C CS Ensembl:ENSG00000062485 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs552952131 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11986982 RMVar_hsa_circ_117890,RMVar_hsa_circ_157324,RMVar_hsa_circ_82371,RMVar_hsa_circ_157325,RMVar_hsa_circ_8991,RMVar_hsa_circ_83353,RMVar_hsa_circ_106144,RMVar_hsa_circ_92622,RMVar_hsa_circ_157329,RMVar_hsa_circ_10990,RMVar_hsa_circ_157328,RMVar_hsa_circ_277144,RMVar_hsa_circ_27216,RMVar_hsa_circ_157334,RMVar_hsa_circ_157335,RMVar_hsa_circ_365232,RMVar_hsa_circ_331502 33988 RMVar_ID_33988 Human_SNP_ID_502369578 A-to-I Human chr12 - 56285576 56285576 56285576 ACAATAAGAAAAGGAATCAAACAGAGGGCGCAATGGCTCATGCCTATTATCCCAACATTTTGGGA ACAATAAGAAAAGGAATCAAACAGAGGGCGCAGTGGCTCATGCCTATTATCCCAACATTTTGGGA T C CS Ensembl:ENSG00000062485 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1430785260 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11986982 RMVar_hsa_circ_117890,RMVar_hsa_circ_157324,RMVar_hsa_circ_82371,RMVar_hsa_circ_157325,RMVar_hsa_circ_8991,RMVar_hsa_circ_83353,RMVar_hsa_circ_106144,RMVar_hsa_circ_92622,RMVar_hsa_circ_157329,RMVar_hsa_circ_10990,RMVar_hsa_circ_157328,RMVar_hsa_circ_277144,RMVar_hsa_circ_27216,RMVar_hsa_circ_157334,RMVar_hsa_circ_157335,RMVar_hsa_circ_365232,RMVar_hsa_circ_331502 33989 RMVar_ID_33989 Human_SNP_ID_502370309 A-to-I Human chr12 - 56288476 56288476 56288476 CAAAAATTAGCCAAGCATGGTGGCGTGTGCCTATAATCCCAGCTACTCAGGAGGCTGAGGCATGA CAAAAATTAGCCAAGCATGGTGGCGTGTGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCATGA T C CS,AC073896.1 Ensembl:ENSG00000062485,Ensembl:ENSG00000144785 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1180183815 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24984089 RMVar_hsa_circ_117890,RMVar_hsa_circ_157324,RMVar_hsa_circ_83353,RMVar_hsa_circ_65934,RMVar_hsa_circ_92622,RMVar_hsa_circ_157328,RMVar_hsa_circ_157335,RMVar_hsa_circ_365232,RMVar_hsa_circ_361093,RMVar_hsa_circ_335439 33990 RMVar_ID_33990 Human_SNP_ID_502370702 A-to-I Human chr12 - 56290175 56290175 56290175 AAACATAAAATCTTCCGGGCACTGTGGCTCATACCTGTAATCCCAGCACTTTGGGAGGCTGAGGC AAACATAAAATCTTCCGGGCACTGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGC T C CS,AC073896.1 Ensembl:ENSG00000062485,Ensembl:ENSG00000144785 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1487545152 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117890,RMVar_hsa_circ_157324,RMVar_hsa_circ_83353,RMVar_hsa_circ_65934,RMVar_hsa_circ_92622,RMVar_hsa_circ_157328,RMVar_hsa_circ_157335,RMVar_hsa_circ_365232,RMVar_hsa_circ_361093,RMVar_hsa_circ_335439 33991 RMVar_ID_33991 Human_SNP_ID_502370734 A-to-I Human chr12 - 56290280 56290278 56290280 GTGAACCTGGGAGAGGGAGGTTGCAATGAGCTAAGATTGTGCCATTGCACTCCAGCCTGGGTGAC GTGAACCTGGGAGAGGGAGGTTGCAATGAGCT__GATTGTGCCATTGCACTCCAGCCTGGGTGAC CTT C CS,AC073896.1 Ensembl:ENSG00000062485,Ensembl:ENSG00000144785 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1483331522 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_117890,RMVar_hsa_circ_157324,RMVar_hsa_circ_83353,RMVar_hsa_circ_65934,RMVar_hsa_circ_92622,RMVar_hsa_circ_157328,RMVar_hsa_circ_157335,RMVar_hsa_circ_365232,RMVar_hsa_circ_361093,RMVar_hsa_circ_335439 33992 RMVar_ID_33992 Human_SNP_ID_502371671 A-to-I Human chr12 - 56294229 56294229 56294229 CCTCAGGTGATCGGCCTACCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGCACC CCTCAGGTGATCGGCCTACCTTGGCCTCCCAAGGTGCTGGGATTACAGGCATGAGCCACTGCACC T C CS,AC073896.1 Ensembl:ENSG00000062485,Ensembl:ENSG00000144785 Protein coding,Protein coding intron,intron GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs1472736583 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83353,RMVar_hsa_circ_92622,RMVar_hsa_circ_157328,RMVar_hsa_circ_157335,RMVar_hsa_circ_365232,RMVar_hsa_circ_361093,RMVar_hsa_circ_335439 33993 RMVar_ID_33993 Human_SNP_ID_502371672 A-to-I Human chr12 - 56294230 56294230 56294230 ACCTCAGGTGATCGGCCTACCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGCAC ACCTCAGGTGATCGGCCTACCTTGGCCTCCCAGAGTGCTGGGATTACAGGCATGAGCCACTGCAC T C CS,AC073896.1 Ensembl:ENSG00000062485,Ensembl:ENSG00000144785 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1303598388 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83353,RMVar_hsa_circ_92622,RMVar_hsa_circ_157328,RMVar_hsa_circ_157335,RMVar_hsa_circ_365232,RMVar_hsa_circ_361093,RMVar_hsa_circ_335439 33994 RMVar_ID_33994 Human_SNP_ID_502372679 A-to-I Human chr12 - 56298133 56298133 56298133 TTAGCCAGACATGGTGGCACATGCCTGTAATCATAGCTACTTGGGAGGCTGAGGCAGGAGGATCG TTAGCCAGACATGGTGGCACATGCCTGTAATCGTAGCTACTTGGGAGGCTGAGGCAGGAGGATCG T C CS,AC073896.1 Ensembl:ENSG00000062485,Ensembl:ENSG00000144785 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs908793860 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83353,RMVar_hsa_circ_92622,RMVar_hsa_circ_157328,RMVar_hsa_circ_157335,RMVar_hsa_circ_365232,RMVar_hsa_circ_361093,RMVar_hsa_circ_335439 33995 RMVar_ID_33995 Human_SNP_ID_502372680 A-to-I Human chr12 - 56298137 56298137 56298137 AAAATTAGCCAGACATGGTGGCACATGCCTGTAATCATAGCTACTTGGGAGGCTGAGGCAGGAGG AAAATTAGCCAGACATGGTGGCACATGCCTGTGATCATAGCTACTTGGGAGGCTGAGGCAGGAGG T C CS,AC073896.1 Ensembl:ENSG00000062485,Ensembl:ENSG00000144785 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs940196221 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83353,RMVar_hsa_circ_92622,RMVar_hsa_circ_157328,RMVar_hsa_circ_157335,RMVar_hsa_circ_365232,RMVar_hsa_circ_361093,RMVar_hsa_circ_335439 33996 RMVar_ID_33996 Human_SNP_ID_502372692 A-to-I Human chr12 - 56298199 56298199 56298199 GAGGTCGGGAATTTGAGACCAGCCTGACCAACATGGAGAAACCTCATCTCTACGAAAAATACAAA GAGGTCGGGAATTTGAGACCAGCCTGACCAACGTGGAGAAACCTCATCTCTACGAAAAATACAAA T C CS,AC073896.1 Ensembl:ENSG00000062485,Ensembl:ENSG00000144785 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1177317065 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24984185 RMVar_hsa_circ_83353,RMVar_hsa_circ_92622,RMVar_hsa_circ_157328,RMVar_hsa_circ_157335,RMVar_hsa_circ_365232,RMVar_hsa_circ_361093,RMVar_hsa_circ_335439 33997 RMVar_ID_33997 Human_SNP_ID_502374070 A-to-I Human chr12 - 56303490 56303490 56303490 AGGTGTGGTGGTGAGTACCTGTAGTCCCAGCTACTTGGGAGAGTGAGGTGGGAGGATCGCTTGAG AGGTGTGGTGGTGAGTACCTGTAGTCCCAGCTCCTTGGGAGAGTGAGGTGGGAGGATCGCTTGAG T G AC073896.1 Ensembl:ENSG00000144785 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs974579955 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25024975 33998 RMVar_ID_33998 Human_SNP_ID_502374300 A-to-I Human chr12 - 56304219 56304219 56304219 TTTTATGTTTTTTTTAGAGAAAAGGTCTCACTATGTTGCCCAATCTGGAGTACAGTGGCTGTTCA TTTTATGTTTTTTTTAGAGAAAAGGTCTCACTGTGTTGCCCAATCTGGAGTACAGTGGCTGTTCA T C AC073896.1 Ensembl:ENSG00000144785 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1362582921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6200918 33999 RMVar_ID_33999 Human_SNP_ID_502374354 A-to-I Human chr12 - 56304470 56304470 56304470 GTTGCCCAGGGTGGACTTGAATTCCTGGTCTCAGGTGATCCTCCTGCCTTGGCCTTCCAAAGTGC GTTGCCCAGGGTGGACTTGAATTCCTGGTCTCGGGTGATCCTCCTGCCTTGGCCTTCCAAAGTGC T C AC073896.1 Ensembl:ENSG00000144785 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973201249 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24984230 34000 RMVar_ID_34000 Human_SNP_ID_502375044 A-to-I Human chr12 - 56307401 56307401 56307401 TCATTGCAGCCTCTAACTCCTGGCTTCAAGCAATCCTCCTGCCTTGGCCTCCTGAGTTTCTAGGA TCATTGCAGCCTCTAACTCCTGGCTTCAAGCAGTCCTCCTGCCTTGGCCTCCTGAGTTTCTAGGA T C AC073896.1 Ensembl:ENSG00000144785 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1030197102 Functional Loss SNV dbSNP153 33..33 33 - - - 34001 RMVar_ID_34001 Human_SNP_ID_502375229 A-to-I Human chr12 - 56308259 56308259 56308259 TGCTACAAAAAATACAAAAATTAGCCGGCATAATGGTGTGCACCTGTGGTTCCAGCGACTCTGGA TGCTACAAAAAATACAAAAATTAGCCGGCATAGTGGTGTGCACCTGTGGTTCCAGCGACTCTGGA T C AC073896.1 Ensembl:ENSG00000144785 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs568387476 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6200951 34002 RMVar_ID_34002 Human_SNP_ID_502375240 A-to-I Human chr12 - 56308304 56308304 56308304 GTCCAGGAGTTTGAGACCAGCCTAGGCAATATAGTGAGACCCCATTGCTACAAAAAATACAAAAA GTCCAGGAGTTTGAGACCAGCCTAGGCAATATTGTGAGACCCCATTGCTACAAAAAATACAAAAA T A AC073896.1 Ensembl:ENSG00000144785 Protein coding intron GSE100210;GSE112787 HepG2 cell line;293 Flip-In T-REx cells,empty vector - 29129909,29967493 RNA-Seq:(High) rs1565626908 Functional Loss SNV dbSNP153 33..33 33 - - - 34003 RMVar_ID_34003 Human_SNP_ID_502375241 A-to-I Human chr12 - 56308313 56308313 56308313 ATCACTCGAGTCCAGGAGTTTGAGACCAGCCTAGGCAATATAGTGAGACCCCATTGCTACAAAAA ATCACTCGAGTCCAGGAGTTTGAGACCAGCCTGGGCAATATAGTGAGACCCCATTGCTACAAAAA T C AC073896.1 Ensembl:ENSG00000144785 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1406684832 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_423959,Human_RBP_ID_11987771,Human_RBP_ID_23566840 34004 RMVar_ID_34004 Human_SNP_ID_502376168 A-to-I Human chr12 - 56311654 56311654 56311654 CCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCCAGGAGGCAGAGGTTGCAATAAGC CCAGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACCCAGGAGGCAGAGGTTGCAATAAGC T C CNPY2,AC073896.1 Ensembl:ENSG00000257727,Ensembl:ENSG00000144785 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs890330130 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24984328 34005 RMVar_ID_34005 Human_SNP_ID_502376171 A-to-I Human chr12 - 56311676 56311676 56311676 GTGGTGGTGCATGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCCA GTGGTGGTGCATGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCCA T C CNPY2,AC073896.1 Ensembl:ENSG00000257727,Ensembl:ENSG00000144785 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1364729644 Functional Loss SNV dbSNP153 33..33 33 - - - 34006 RMVar_ID_34006 Human_SNP_ID_502376196 A-to-I Human chr12 - 56311740 56311740 56311740 TGAGACCAGCCCGACCAACACAGAGAAACCCCATCTCTACTAAAAATACAAAAGTTAGCTGGGTG TGAGACCAGCCCGACCAACACAGAGAAACCCCGTCTCTACTAAAAATACAAAAGTTAGCTGGGTG T C CNPY2,AC073896.1 Ensembl:ENSG00000257727,Ensembl:ENSG00000144785 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1241161398 Functional Loss SNV dbSNP153 33..33 33 - - - 34007 RMVar_ID_34007 Human_SNP_ID_502376200 A-to-I Human chr12 - 56311751 56311750 56311752 GGTCTGGAGTTTGAGACCAGCCCGACCAACACAGAGAAACCCCATCTCTACTAAAAATACAAAAG GGTCTGGAGTTTGAGACCAGCCCGACCAACA__GAGAAACCCCATCTCTACTAAAAATACAAAAG CTG C CNPY2,AC073896.1 Ensembl:ENSG00000257727,Ensembl:ENSG00000144785 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1368975865 Functional Loss DEL dbSNP153 32..33 33 - - - 34008 RMVar_ID_34008 Human_SNP_ID_502376628 A-to-I Human chr12 - 56313274 56313274 56313274 GTTGGTCAGGATGGTCTCGAACTCCTGACCTCAAGTGAGCCACCCTCCTCGGCCTCTCAAAGTGC GTTGGTCAGGATGGTCTCGAACTCCTGACCTCCAGTGAGCCACCCTCCTCGGCCTCTCAAAGTGC T G CNPY2,AC073896.1 Ensembl:ENSG00000257727,Ensembl:ENSG00000144785 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1221358701 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24984350 34009 RMVar_ID_34009 Human_SNP_ID_502376824 A-to-I Human chr12 - 56314040 56314040 56314040 AAAAGTAGCCAGGCGTGGTGGCTCATGCCTATAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGA AAAAGTAGCCAGGCGTGGTGGCTCATGCCTATGGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGA T C CNPY2,AC073896.1 Ensembl:ENSG00000257727,Ensembl:ENSG00000144785 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1198706559 Functional Loss SNV dbSNP153 33..33 33 - - - 34010 RMVar_ID_34010 Human_SNP_ID_502387312 A-to-I Human chr12 - 56353828 56353828 56353828 CCATGCCTGGCTAGTTTTTTTGTATTTTTAGTAGAGACGATGTTTCTCCATGTTGGCCAGGCTGG CCATGCCTGGCTAGTTTTTTTGTATTTTTAGTGGAGACGATGTTTCTCCATGTTGGCCAGGCTGG T C STAT2 Ensembl:ENSG00000170581 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1565656851 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3626,RMVar_hsa_circ_110793,RMVar_hsa_circ_157343,RMVar_hsa_circ_42097,RMVar_hsa_circ_62643,RMVar_hsa_circ_20152,RMVar_hsa_circ_157352,RMVar_hsa_circ_374080,RMVar_hsa_circ_47377,RMVar_hsa_circ_101334,RMVar_hsa_circ_157354,RMVar_hsa_circ_21301,RMVar_hsa_circ_119937,RMVar_hsa_circ_157356,RMVar_hsa_circ_117212,RMVar_hsa_circ_157359,RMVar_hsa_circ_110178,RMVar_hsa_circ_267051,RMVar_hsa_circ_157361 34011 RMVar_ID_34011 Human_SNP_ID_502387341 A-to-I Human chr12 - 56353909 56353909 56353909 TCACTGCAACTTCCAACTCCCAGGTTCAAGCAATTCTCCTGTCTCAGCCTCCCGAGTTGCTGGGA TCACTGCAACTTCCAACTCCCAGGTTCAAGCAGTTCTCCTGTCTCAGCCTCCCGAGTTGCTGGGA T C STAT2 Ensembl:ENSG00000170581 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1307785599 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3626,RMVar_hsa_circ_110793,RMVar_hsa_circ_157343,RMVar_hsa_circ_42097,RMVar_hsa_circ_62643,RMVar_hsa_circ_20152,RMVar_hsa_circ_157352,RMVar_hsa_circ_374080,RMVar_hsa_circ_47377,RMVar_hsa_circ_101334,RMVar_hsa_circ_157354,RMVar_hsa_circ_21301,RMVar_hsa_circ_119937,RMVar_hsa_circ_157356,RMVar_hsa_circ_117212,RMVar_hsa_circ_157359,RMVar_hsa_circ_110178,RMVar_hsa_circ_267051,RMVar_hsa_circ_157361 34012 RMVar_ID_34012 Human_SNP_ID_502402343 A-to-I Human chr12 - 56415891 56415891 56415891 ATTTTTTGTATTTTTAGTAGAGACAGGATTTCACCACGTTGGCCAGGCTGGTCTTGAACTCCTGA ATTTTTTGTATTTTTAGTAGAGACAGGATTTCGCCACGTTGGCCAGGCTGGTCTTGAACTCCTGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs549770284 Functional Loss SNV dbSNP153 33..33 33 - - - 34013 RMVar_ID_34013 Human_SNP_ID_502402629 A-to-I Human chr12 - 56416917 56416917 56416917 GAGTTTGAGACCGGCCTGGACAATATGGCGAAATCCCATCTCCACTAAAAATACAAAAATTAGCC GAGTTTGAGACCGGCCTGGACAATATGGCGAAGTCCCATCTCCACTAAAAATACAAAAATTAGCC T C TIMELESS Ensembl:ENSG00000111602 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985757169 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11988346 RMVar_hsa_circ_106918,RMVar_hsa_circ_157363 34014 RMVar_ID_34014 Human_SNP_ID_502404273 A-to-I Human chr12 - 56421911 56421911 56421911 TCTGGTACAGATGGGACTGGCTGACAGTGTCAAGGACTTCCAAAGGTAGAGAGGCACATGCTCTG TCTGGTACAGATGGGACTGGCTGACAGTGTCAGGGACTTCCAAAGGTAGAGAGGCACATGCTCTG T C TIMELESS Ensembl:ENSG00000111602 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1362318641 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_424057,Human_RBP_ID_8783540,Human_RBP_ID_17823122,Human_RBP_ID_18977404,Human_RBP_ID_26323012 Human_Splice_Rec_1384265,Human_Splice_Rec_1384321,Human_Splice_Rec_1384349 Human_miRNA_ID_2782650,Human_miRNA_ID_2785618 RMVar_hsa_circ_106918,RMVar_hsa_circ_110364,RMVar_hsa_circ_157363,RMVar_hsa_circ_265341,RMVar_hsa_circ_157364 34015 RMVar_ID_34015 Human_SNP_ID_502418789 A-to-I Human chr12 + 56476696 56476696 56476696 GCTCAACTGCAAGCTCCGCCTCCCGGGTTCATACCATTCTCCTGCCTTAGCCTCCCGAGCAGCTG GCTCAACTGCAAGCTCCGCCTCCCGGGTTCATGCCATTCTCCTGCCTTAGCCTCCCGAGCAGCTG A G SPRYD4 Ensembl:ENSG00000176422 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1468903716 Functional Loss SNV dbSNP153 33..33 33 - - - 34016 RMVar_ID_34016 Human_SNP_ID_502427691 A-to-I Human chr12 + 56511523 56511523 56511523 ACCACCCCTGAAGAAATTGCACAGGTTGCTACAATTTCTGCAAACGGAGACAAAGAAATTGGCAA ACCACCCCTGAAGAAATTGCACAGGTTGCTACCATTTCTGCAAACGGAGACAAAGAAATTGGCAA A C HSPD1P4 Ensembl:ENSG00000257576 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031775824 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17358678 34017 RMVar_ID_34017 Human_SNP_ID_502431347 A-to-I Human chr12 + 56528017 56528017 56528017 CATGCCTGTAATTCCAGCACTTTGGGAGGCCAAAGTGGGAGGATCACTTGACCTAGGAGTTCCAG CATGCCTGTAATTCCAGCACTTTGGGAGGCCACAGTGGGAGGATCACTTGACCTAGGAGTTCCAG A C RBMS2 Ensembl:ENSG00000076067 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1287419170 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105227,RMVar_hsa_circ_120797,RMVar_hsa_circ_109066,RMVar_hsa_circ_157378,RMVar_hsa_circ_157380,RMVar_hsa_circ_98915,RMVar_hsa_circ_157379,RMVar_hsa_circ_157377 34018 RMVar_ID_34018 Human_SNP_ID_502437934 A-to-I Human chr12 + 56556475 56556475 56556475 TGGGCTCACTGCAACCTCTGCCTCCCGAGTTCAAGCGATTCTCCTGCCTCAGCCTCTGGAGTAGC TGGGCTCACTGCAACCTCTGCCTCCCGAGTTCGAGCGATTCTCCTGCCTCAGCCTCTGGAGTAGC A G RBMS2 Ensembl:ENSG00000076067 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1378606776 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105227,RMVar_hsa_circ_120797,RMVar_hsa_circ_109066,RMVar_hsa_circ_157378,RMVar_hsa_circ_157380,RMVar_hsa_circ_98915,RMVar_hsa_circ_157379,RMVar_hsa_circ_157377 34019 RMVar_ID_34019 Human_SNP_ID_502438137 A-to-I Human chr12 + 56557539 56557539 56557539 TACCTCCTGATGAGAGGGACCAGTCCCACAGTATTTTTGCTGACTGTAAGCTCAATAAAGGCAGA TACCTCCTGATGAGAGGGACCAGTCCCACAGTGTTTTTGCTGACTGTAAGCTCAATAAAGGCAGA A G RBMS2 Ensembl:ENSG00000076067 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs902883837 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105227,RMVar_hsa_circ_120797,RMVar_hsa_circ_109066,RMVar_hsa_circ_157378,RMVar_hsa_circ_157380,RMVar_hsa_circ_98915,RMVar_hsa_circ_157379,RMVar_hsa_circ_157377 34020 RMVar_ID_34020 Human_SNP_ID_502439138 A-to-I Human chr12 + 56561098 56561098 56561098 TCCAACCATGTTCCTGCAAAGGACAGGATCTCATTCTTCTTTATGGCTCCGTAGTATTCCATGTG TCCAACCATGTTCCTGCAAAGGACAGGATCTCGTTCTTCTTTATGGCTCCGTAGTATTCCATGTG A G RBMS2 Ensembl:ENSG00000076067 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs537927224 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105227,RMVar_hsa_circ_120797,RMVar_hsa_circ_109066,RMVar_hsa_circ_157378,RMVar_hsa_circ_157380,RMVar_hsa_circ_98915,RMVar_hsa_circ_157379,RMVar_hsa_circ_157377 34021 RMVar_ID_34021 Human_SNP_ID_502442169 A-to-I Human chr12 + 56573865 56573865 56573865 TTTTTGTTGTTGTTGTTGTTGTTGTTGAGACGAAGTCTCACTCTGTTGCCCAGGCTGGAGTGCAA TTTTTGTTGTTGTTGTTGTTGTTGTTGAGACGCAGTCTCACTCTGTTGCCCAGGCTGGAGTGCAA A C RBMS2 Ensembl:ENSG00000076067 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947095213 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105227,RMVar_hsa_circ_109066,RMVar_hsa_circ_125421,RMVar_hsa_circ_157378,RMVar_hsa_circ_98915,RMVar_hsa_circ_157379,RMVar_hsa_circ_157377,RMVar_hsa_circ_373994,RMVar_hsa_circ_305741,RMVar_hsa_circ_318255,RMVar_hsa_circ_118978,RMVar_hsa_circ_116716,RMVar_hsa_circ_157385,RMVar_hsa_circ_157387,RMVar_hsa_circ_157388,RMVar_hsa_circ_157389,RMVar_hsa_circ_157386,RMVar_hsa_circ_322103,RMVar_hsa_circ_345345,RMVar_hsa_circ_113401,RMVar_hsa_circ_157391,RMVar_hsa_circ_157392,RMVar_hsa_circ_115004,RMVar_hsa_circ_118516,RMVar_hsa_circ_109041,RMVar_hsa_circ_86313,RMVar_hsa_circ_157394,RMVar_hsa_circ_157395,RMVar_hsa_circ_157393,RMVar_hsa_circ_157396 34022 RMVar_ID_34022 Human_SNP_ID_502442231 A-to-I Human chr12 + 56574121 56574121 56574121 CCTCAGCCTCCCAAAGTGCTAGGATTACAGGCATGAGCCACTGCGCCCAGCCAGTCCACACAACT CCTCAGCCTCCCAAAGTGCTAGGATTACAGGCGTGAGCCACTGCGCCCAGCCAGTCCACACAACT A G RBMS2 Ensembl:ENSG00000076067 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1178191515 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105227,RMVar_hsa_circ_109066,RMVar_hsa_circ_125421,RMVar_hsa_circ_157378,RMVar_hsa_circ_98915,RMVar_hsa_circ_157379,RMVar_hsa_circ_157377,RMVar_hsa_circ_373994,RMVar_hsa_circ_305741,RMVar_hsa_circ_318255,RMVar_hsa_circ_118978,RMVar_hsa_circ_116716,RMVar_hsa_circ_157385,RMVar_hsa_circ_157387,RMVar_hsa_circ_157388,RMVar_hsa_circ_157389,RMVar_hsa_circ_157386,RMVar_hsa_circ_322103,RMVar_hsa_circ_345345,RMVar_hsa_circ_113401,RMVar_hsa_circ_157391,RMVar_hsa_circ_157392,RMVar_hsa_circ_115004,RMVar_hsa_circ_118516,RMVar_hsa_circ_109041,RMVar_hsa_circ_86313,RMVar_hsa_circ_157394,RMVar_hsa_circ_157395,RMVar_hsa_circ_157393,RMVar_hsa_circ_157396 34023 RMVar_ID_34023 Human_SNP_ID_502442957 A-to-I Human chr12 + 56577331 56577331 56577331 TACTCAGGAGTCTGAGGCAGGAGAATCATTTGAACCCAGGAGGCAGAAGTTGCAGTGAGCCGAGA TACTCAGGAGTCTGAGGCAGGAGAATCATTTGGACCCAGGAGGCAGAAGTTGCAGTGAGCCGAGA A G RBMS2 Ensembl:ENSG00000076067 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1186399741 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105227,RMVar_hsa_circ_109066,RMVar_hsa_circ_125421,RMVar_hsa_circ_157378,RMVar_hsa_circ_98915,RMVar_hsa_circ_157379,RMVar_hsa_circ_157377,RMVar_hsa_circ_373994,RMVar_hsa_circ_305741,RMVar_hsa_circ_318255,RMVar_hsa_circ_118978,RMVar_hsa_circ_116716,RMVar_hsa_circ_157385,RMVar_hsa_circ_157387,RMVar_hsa_circ_157388,RMVar_hsa_circ_157389,RMVar_hsa_circ_157386,RMVar_hsa_circ_322103,RMVar_hsa_circ_345345,RMVar_hsa_circ_113401,RMVar_hsa_circ_157391,RMVar_hsa_circ_157392,RMVar_hsa_circ_115004,RMVar_hsa_circ_118516,RMVar_hsa_circ_109041,RMVar_hsa_circ_86313,RMVar_hsa_circ_157394,RMVar_hsa_circ_157395,RMVar_hsa_circ_157393,RMVar_hsa_circ_157396 34024 RMVar_ID_34024 Human_SNP_ID_502443577 A-to-I Human chr12 + 56579999 56579999 56579999 TCACCTAGGCTGGAGTGCAGTGGCATGATCTCAGCTCACTGCAGCCTCTGCTTCCCAGGTTCAAG TCACCTAGGCTGGAGTGCAGTGGCATGATCTCGGCTCACTGCAGCCTCTGCTTCCCAGGTTCAAG A G RBMS2 Ensembl:ENSG00000076067 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1168660275 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105227,RMVar_hsa_circ_109066,RMVar_hsa_circ_125421,RMVar_hsa_circ_157378,RMVar_hsa_circ_98915,RMVar_hsa_circ_157379,RMVar_hsa_circ_157377,RMVar_hsa_circ_373994,RMVar_hsa_circ_305741,RMVar_hsa_circ_318255,RMVar_hsa_circ_118978,RMVar_hsa_circ_116716,RMVar_hsa_circ_157385,RMVar_hsa_circ_157387,RMVar_hsa_circ_157388,RMVar_hsa_circ_157389,RMVar_hsa_circ_157386,RMVar_hsa_circ_322103,RMVar_hsa_circ_345345,RMVar_hsa_circ_113401,RMVar_hsa_circ_157391,RMVar_hsa_circ_157392,RMVar_hsa_circ_115004,RMVar_hsa_circ_118516,RMVar_hsa_circ_109041,RMVar_hsa_circ_86313,RMVar_hsa_circ_157394,RMVar_hsa_circ_157395,RMVar_hsa_circ_157393,RMVar_hsa_circ_157396 34025 RMVar_ID_34025 Human_SNP_ID_502444619 A-to-I Human chr12 + 56584286 56584286 56584286 AAACCCCTGTCCCTACAAAAAATACAAAAATTAGCCAGGTGAGGTGGTGCGTGCCTGTAATCCCA AAACCCCTGTCCCTACAAAAAATACAAAAATTGGCCAGGTGAGGTGGTGCGTGCCTGTAATCCCA A G RBMS2 Ensembl:ENSG00000076067 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs897298686 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109066,RMVar_hsa_circ_125421,RMVar_hsa_circ_157378,RMVar_hsa_circ_98915,RMVar_hsa_circ_157377,RMVar_hsa_circ_373994,RMVar_hsa_circ_318255,RMVar_hsa_circ_118978,RMVar_hsa_circ_157387,RMVar_hsa_circ_157388,RMVar_hsa_circ_157389,RMVar_hsa_circ_157386,RMVar_hsa_circ_322103,RMVar_hsa_circ_157392,RMVar_hsa_circ_118516,RMVar_hsa_circ_109041,RMVar_hsa_circ_85919,RMVar_hsa_circ_88210,RMVar_hsa_circ_86313,RMVar_hsa_circ_157394,RMVar_hsa_circ_157393,RMVar_hsa_circ_157396,RMVar_hsa_circ_328413,RMVar_hsa_circ_157397,RMVar_hsa_circ_371914,RMVar_hsa_circ_157399,RMVar_hsa_circ_157400,RMVar_hsa_circ_157401,RMVar_hsa_circ_94903,RMVar_hsa_circ_157403,RMVar_hsa_circ_90982,RMVar_hsa_circ_85661,RMVar_hsa_circ_111570,RMVar_hsa_circ_157404,RMVar_hsa_circ_157405,RMVar_hsa_circ_157406 34026 RMVar_ID_34026 Human_SNP_ID_502449092 A-to-I Human chr12 - 56600463 56600463 56600463 TGAAGGGCTGGACATGTCCTAGCCCAGACTCTACCCGTGAAGACTTGGCCTACTGTGAGCACCTC TGAAGGGCTGGACATGTCCTAGCCCAGACTCTTCCCGTGAAGACTTGGCCTACTGTGAGCACCTC T A BAZ2A Ensembl:ENSG00000076108 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs772642986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229704,Human_RBP_ID_1797856,Human_RBP_ID_8783619,Human_RBP_ID_18977431,Human_RBP_ID_19056417,Human_RBP_ID_22472006,Human_RBP_ID_27423680 Human_Splice_Rec_1384898,Human_Splice_Rec_1384954,Human_Splice_Rec_1384978,Human_Splice_Rec_1385034,Human_Splice_Rec_1385050 RMVar_hsa_circ_60919 34027 RMVar_ID_34027 Human_SNP_ID_502449093 A-to-I Human chr12 - 56600463 56600463 56600463 TGAAGGGCTGGACATGTCCTAGCCCAGACTCTACCCGTGAAGACTTGGCCTACTGTGAGCACCTC TGAAGGGCTGGACATGTCCTAGCCCAGACTCTGCCCGTGAAGACTTGGCCTACTGTGAGCACCTC T C BAZ2A Ensembl:ENSG00000076108 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs772642986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_229704,Human_RBP_ID_1797856,Human_RBP_ID_8783619,Human_RBP_ID_18977431,Human_RBP_ID_19056417,Human_RBP_ID_22472006,Human_RBP_ID_27423680 Human_Splice_Rec_1384898,Human_Splice_Rec_1384954,Human_Splice_Rec_1384978,Human_Splice_Rec_1385034,Human_Splice_Rec_1385050 RMVar_hsa_circ_60919 34028 RMVar_ID_34028 Human_SNP_ID_502451348 A-to-I Human chr12 - 56608035 56608035 56608035 AGTTTTGCTCTTGTTGCCCAGGCTGGAGTGCAATGGCGCGATCTTGGCTCACCGCAACCTCCCAG AGTTTTGCTCTTGTTGCCCAGGCTGGAGTGCAGTGGCGCGATCTTGGCTCACCGCAACCTCCCAG T C BAZ2A Ensembl:ENSG00000076108 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1238886116 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89965,RMVar_hsa_circ_157412,RMVar_hsa_circ_95702,RMVar_hsa_circ_157414,RMVar_hsa_circ_58360,RMVar_hsa_circ_111422,RMVar_hsa_circ_157418 34029 RMVar_ID_34029 Human_SNP_ID_502451436 A-to-I Human chr12 - 56608285 56608285 56608285 TCACTACAAGCTCTGCCTCCTGGATTCACCCCATTCTCCTGCCTCGGCCTCCCGAGTAGCTGGGA TCACTACAAGCTCTGCCTCCTGGATTCACCCCGTTCTCCTGCCTCGGCCTCCCGAGTAGCTGGGA T C BAZ2A Ensembl:ENSG00000076108 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1565817928 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25025072 RMVar_hsa_circ_89965,RMVar_hsa_circ_157412,RMVar_hsa_circ_95702,RMVar_hsa_circ_157414,RMVar_hsa_circ_58360,RMVar_hsa_circ_111422,RMVar_hsa_circ_157418 34030 RMVar_ID_34030 Human_SNP_ID_502451528 A-to-I Human chr12 - 56608617 56608617 56608617 TGCAGTGAGCTGAGATCACACCATTGCACTCCAGCCTGGGCAACAAGAGTGAAACTCCATCTCAA TGCAGTGAGCTGAGATCACACCATTGCACTCCGGCCTGGGCAACAAGAGTGAAACTCCATCTCAA T C BAZ2A Ensembl:ENSG00000076108 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs928990829 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89965,RMVar_hsa_circ_157412,RMVar_hsa_circ_95702,RMVar_hsa_circ_157414,RMVar_hsa_circ_58360,RMVar_hsa_circ_111422,RMVar_hsa_circ_157418 34031 RMVar_ID_34031 Human_SNP_ID_502451529 A-to-I Human chr12 - 56608617 56608617 56608617 TGCAGTGAGCTGAGATCACACCATTGCACTCCAGCCTGGGCAACAAGAGTGAAACTCCATCTCAA TGCAGTGAGCTGAGATCACACCATTGCACTCCCGCCTGGGCAACAAGAGTGAAACTCCATCTCAA T G BAZ2A Ensembl:ENSG00000076108 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs928990829 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89965,RMVar_hsa_circ_157412,RMVar_hsa_circ_95702,RMVar_hsa_circ_157414,RMVar_hsa_circ_58360,RMVar_hsa_circ_111422,RMVar_hsa_circ_157418 34032 RMVar_ID_34032 Human_SNP_ID_502451533 A-to-I Human chr12 - 56608630 56608630 56608630 AGGAGGCAGAGGTTGCAGTGAGCTGAGATCACACCATTGCACTCCAGCCTGGGCAACAAGAGTGA AGGAGGCAGAGGTTGCAGTGAGCTGAGATCACGCCATTGCACTCCAGCCTGGGCAACAAGAGTGA T C BAZ2A Ensembl:ENSG00000076108 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1365513700 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89965,RMVar_hsa_circ_157412,RMVar_hsa_circ_95702,RMVar_hsa_circ_157414,RMVar_hsa_circ_58360,RMVar_hsa_circ_111422,RMVar_hsa_circ_157418 34033 RMVar_ID_34033 Human_SNP_ID_502451550 A-to-I Human chr12 - 56608707 56608707 56608707 AAATTAGCCAGGCATGGTGGCGCATGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAA AAATTAGCCAGGCATGGTGGCGCATGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAA T C BAZ2A Ensembl:ENSG00000076108 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1214984919 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89965,RMVar_hsa_circ_157412,RMVar_hsa_circ_95702,RMVar_hsa_circ_157414,RMVar_hsa_circ_58360,RMVar_hsa_circ_111422,RMVar_hsa_circ_157418 34034 RMVar_ID_34034 Human_SNP_ID_502451551 A-to-I Human chr12 - 56608708 56608708 56608708 AAAATTAGCCAGGCATGGTGGCGCATGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTAGCCAGGCATGGTGGCGCATGCCTGTGATCCCAGCTACTCGGGAGGCTGAGGCAGGAGA T C BAZ2A Ensembl:ENSG00000076108 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs890104010 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89965,RMVar_hsa_circ_157412,RMVar_hsa_circ_95702,RMVar_hsa_circ_157414,RMVar_hsa_circ_58360,RMVar_hsa_circ_111422,RMVar_hsa_circ_157418 34035 RMVar_ID_34035 Human_SNP_ID_502459830 A-to-I Human chr12 - 56640989 56640989 56640989 GCTACAGTGTGGTAGCACAGTCTTGGCTCACTATAACCTCCACCTCCTGGGTTCAAGCGATTCAC GCTACAGTGTGGTAGCACAGTCTTGGCTCACTGTAACCTCCACCTCCTGGGTTCAAGCGATTCAC T C ATP5F1B Ensembl:ENSG00000110955 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs935904279 Functional Loss SNV dbSNP153 33..33 33 - - - 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 34036 RMVar_ID_34036 Human_SNP_ID_502459899 A-to-I Human chr12 - 56641253 56641253 56641253 TCAGGTGATTCCTTTGTCTCAGCCTCCTGAGTAGCTGGGATTATAGGTGCCCGACACCAGGCCCG TCAGGTGATTCCTTTGTCTCAGCCTCCTGAGTGGCTGGGATTATAGGTGCCCGACACCAGGCCCG T C ATP5F1B Ensembl:ENSG00000110955 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1160405370 Functional Loss SNV dbSNP153 33..33 33 - - - 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 34037 RMVar_ID_34037 Human_SNP_ID_502460034 A-to-I Human chr12 - 56641740 56641740 56641740 AAGACCATCCTGACTTAACACAGTGAAACCCCATCTCTACTAAAAATACAAAAAATTAGCTGGGC AAGACCATCCTGACTTAACACAGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTAGCTGGGC T C ATP5F1B Ensembl:ENSG00000110955 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs759360737 Functional Loss SNV dbSNP153 33..33 33 - - - 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 34038 RMVar_ID_34038 Human_SNP_ID_502465299 A-to-I Human chr12 - 56660809 56660809 56660809 CACTGCAATCTCTGAATTCCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTTCCGAGTAGCTGGGA CACTGCAATCTCTGAATTCCCAGGTTCAAGCACTTCTCCTGCCTCAGCCTTCCGAGTAGCTGGGA T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs566331717 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24985304 34039 RMVar_ID_34039 Human_SNP_ID_502467798 A-to-I Human chr12 - 56668025 56668025 56668025 TGGCTCACTCCAGCCTCCACCTCCTGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGCT TGGCTCACTCCAGCCTCCACCTCCTGGGTTCAGGCAATTCTCCTGCCTCAGCCTCCCAAGTAGCT T C PTGES3 Ensembl:ENSG00000110958 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1565860239 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_157452,RMVar_hsa_circ_31608,RMVar_hsa_circ_265226,RMVar_hsa_circ_374821,RMVar_hsa_circ_265153,RMVar_hsa_circ_269992,RMVar_hsa_circ_349993,RMVar_hsa_circ_157451,RMVar_hsa_circ_271848,RMVar_hsa_circ_157453 34040 RMVar_ID_34040 Human_SNP_ID_502467825 A-to-I Human chr12 - 56668116 56668112 56668116 TGAAATCTACTCTTTTAACAGACTATTTATTTATTTTTTTGAGGCAGAGTTTTGCTCTTGTTGCC TGAAATCTACTCTTTTAACAGACTATTTATTT____TTTTGAGGCAGAGTTTTGCTCTTGTTGCC AAAAT A PTGES3 Ensembl:ENSG00000110958 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs761630579 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_9691740,Human_RBP_ID_11990393,Human_RBP_ID_24985427 RMVar_hsa_circ_157452,RMVar_hsa_circ_31608,RMVar_hsa_circ_265226,RMVar_hsa_circ_374821,RMVar_hsa_circ_265153,RMVar_hsa_circ_269992,RMVar_hsa_circ_349993,RMVar_hsa_circ_157451,RMVar_hsa_circ_271848,RMVar_hsa_circ_157453 34041 RMVar_ID_34041 Human_SNP_ID_502467953 A-to-I Human chr12 - 56668504 56668504 56668504 GAACTCCTGAGCTCAAGTGATCCTCCTGCCTCAGCTTCCCAAAGTGCTGGGACTACAGGCCTGAG GAACTCCTGAGCTCAAGTGATCCTCCTGCCTCCGCTTCCCAAAGTGCTGGGACTACAGGCCTGAG T G PTGES3 Ensembl:ENSG00000110958 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1481603595 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_157452,RMVar_hsa_circ_31608,RMVar_hsa_circ_265226,RMVar_hsa_circ_374821,RMVar_hsa_circ_265153,RMVar_hsa_circ_269992,RMVar_hsa_circ_349993,RMVar_hsa_circ_157451,RMVar_hsa_circ_271848,RMVar_hsa_circ_157453 34042 RMVar_ID_34042 Human_SNP_ID_502467960 A-to-I Human chr12 - 56668527 56668527 56668527 ATTGTGTTGCTTAGGCAGGTCTTGAACTCCTGAGCTCAAGTGATCCTCCTGCCTCAGCTTCCCAA ATTGTGTTGCTTAGGCAGGTCTTGAACTCCTGGGCTCAAGTGATCCTCCTGCCTCAGCTTCCCAA T C PTGES3 Ensembl:ENSG00000110958 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs988548616 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_157452,RMVar_hsa_circ_31608,RMVar_hsa_circ_265226,RMVar_hsa_circ_374821,RMVar_hsa_circ_265153,RMVar_hsa_circ_269992,RMVar_hsa_circ_349993,RMVar_hsa_circ_157451,RMVar_hsa_circ_271848,RMVar_hsa_circ_157453 34043 RMVar_ID_34043 Human_SNP_ID_502468247 A-to-I Human chr12 - 56669347 56669344 56669347 CCCAGAAGGCGTGAACAAAATTAGCTGGGCGTAGTGGTGCATGCCTGTGATTCCAGCTACTCGGG CCCAGAAGGCGTGAACAAAATTAGCTGGGCGT___GGTGCATGCCTGTGATTCCAGCTACTCGGG CACT C PTGES3 Ensembl:ENSG00000110958 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1367948689 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_11990465,Human_RBP_ID_22906375 RMVar_hsa_circ_157452,RMVar_hsa_circ_31608,RMVar_hsa_circ_265226,RMVar_hsa_circ_374821,RMVar_hsa_circ_265153,RMVar_hsa_circ_269992,RMVar_hsa_circ_349993,RMVar_hsa_circ_157451,RMVar_hsa_circ_271848,RMVar_hsa_circ_157453 34044 RMVar_ID_34044 Human_SNP_ID_502468248 A-to-I Human chr12 - 56669347 56669347 56669347 CCCAGAAGGCGTGAACAAAATTAGCTGGGCGTAGTGGTGCATGCCTGTGATTCCAGCTACTCGGG CCCAGAAGGCGTGAACAAAATTAGCTGGGCGTGGTGGTGCATGCCTGTGATTCCAGCTACTCGGG T C PTGES3 Ensembl:ENSG00000110958 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1297592390 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11990465,Human_RBP_ID_22906375 RMVar_hsa_circ_157452,RMVar_hsa_circ_31608,RMVar_hsa_circ_265226,RMVar_hsa_circ_374821,RMVar_hsa_circ_265153,RMVar_hsa_circ_269992,RMVar_hsa_circ_349993,RMVar_hsa_circ_157451,RMVar_hsa_circ_271848,RMVar_hsa_circ_157453 34045 RMVar_ID_34045 Human_SNP_ID_502468274 A-to-I Human chr12 - 56669412 56669412 56669412 GGGTGCAGTGGCGGGCGCCTGTAATCTCAGCTACTCAGAAGGCTGAGGCAGGAGAATCGCGTGAA GGGTGCAGTGGCGGGCGCCTGTAATCTCAGCTGCTCAGAAGGCTGAGGCAGGAGAATCGCGTGAA T C PTGES3 Ensembl:ENSG00000110958 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904806361 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_157452,RMVar_hsa_circ_31608,RMVar_hsa_circ_265226,RMVar_hsa_circ_374821,RMVar_hsa_circ_265153,RMVar_hsa_circ_269992,RMVar_hsa_circ_349993,RMVar_hsa_circ_157451,RMVar_hsa_circ_271848,RMVar_hsa_circ_157453 34046 RMVar_ID_34046 Human_SNP_ID_502468776 A-to-I Human chr12 - 56670921 56670921 56670921 TTTTTGTTTTTTCCCCAGATACAGGATCCACTATTGCTCAGGCTGTCTCGAACTCCTGAAGGATT TTTTTGTTTTTTCCCCAGATACAGGATCCACTGTTGCTCAGGCTGTCTCGAACTCCTGAAGGATT T C PTGES3 Ensembl:ENSG00000110958 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs949233841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11990542,Human_RBP_ID_24985492,Human_RBP_ID_27423756 RMVar_hsa_circ_265226,RMVar_hsa_circ_374821,RMVar_hsa_circ_265153,RMVar_hsa_circ_349993,RMVar_hsa_circ_157451,RMVar_hsa_circ_271848,RMVar_hsa_circ_157453,RMVar_hsa_circ_157454,RMVar_hsa_circ_95238,RMVar_hsa_circ_272624,RMVar_hsa_circ_279247,RMVar_hsa_circ_157456,RMVar_hsa_circ_157455 34047 RMVar_ID_34047 Human_SNP_ID_502468864 A-to-I Human chr12 - 56671178 56671178 56671178 CCCAGCTTGGTCTTGAACTTCTGGGCTCAAGCAGTCTCCCCACCTCAGCCTCCCAAAGTGCTGGG CCCAGCTTGGTCTTGAACTTCTGGGCTCAAGCTGTCTCCCCACCTCAGCCTCCCAAAGTGCTGGG T A PTGES3 Ensembl:ENSG00000110958 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1446610545 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9691786,Human_RBP_ID_11990565,Human_RBP_ID_24985497,Human_RBP_ID_26768333 RMVar_hsa_circ_265226,RMVar_hsa_circ_374821,RMVar_hsa_circ_265153,RMVar_hsa_circ_349993,RMVar_hsa_circ_157451,RMVar_hsa_circ_271848,RMVar_hsa_circ_157453,RMVar_hsa_circ_157454,RMVar_hsa_circ_95238,RMVar_hsa_circ_272624,RMVar_hsa_circ_279247,RMVar_hsa_circ_157456,RMVar_hsa_circ_157455 34048 RMVar_ID_34048 Human_SNP_ID_502468876 A-to-I Human chr12 - 56671217 56671217 56671217 ATTTTTGTATTTTTTGTAGAAAGGGGTATCACAGTGTTGCCCAGCTTGGTCTTGAACTTCTGGGC ATTTTTGTATTTTTTGTAGAAAGGGGTATCACTGTGTTGCCCAGCTTGGTCTTGAACTTCTGGGC T A PTGES3 Ensembl:ENSG00000110958 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs888848747 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6201834,Human_RBP_ID_11990567,Human_RBP_ID_26768333 RMVar_hsa_circ_265226,RMVar_hsa_circ_374821,RMVar_hsa_circ_265153,RMVar_hsa_circ_349993,RMVar_hsa_circ_157451,RMVar_hsa_circ_271848,RMVar_hsa_circ_157453,RMVar_hsa_circ_157454,RMVar_hsa_circ_95238,RMVar_hsa_circ_272624,RMVar_hsa_circ_279247,RMVar_hsa_circ_157456,RMVar_hsa_circ_157455 34049 RMVar_ID_34049 Human_SNP_ID_502468894 A-to-I Human chr12 - 56671286 56671286 56671286 CCAAGTGATCCTCCCTCCTCAGTCCCCCAAGTAGCTGGGACTGTAGGGGCATGCCACAACACCTG CCAAGTGATCCTCCCTCCTCAGTCCCCCAAGTGGCTGGGACTGTAGGGGCATGCCACAACACCTG T C PTGES3 Ensembl:ENSG00000110958 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1009774790 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6201836,Human_RBP_ID_11990570,Human_RBP_ID_24985500 RMVar_hsa_circ_265226,RMVar_hsa_circ_374821,RMVar_hsa_circ_265153,RMVar_hsa_circ_349993,RMVar_hsa_circ_157451,RMVar_hsa_circ_271848,RMVar_hsa_circ_157453,RMVar_hsa_circ_157454,RMVar_hsa_circ_95238,RMVar_hsa_circ_272624,RMVar_hsa_circ_279247,RMVar_hsa_circ_157456,RMVar_hsa_circ_157455 34050 RMVar_ID_34050 Human_SNP_ID_502469940 A-to-I Human chr12 - 56674613 56674613 56674613 ATCGTGTTAGCCAGGATGGTCTCAATCTCCTGACATTGTGATCCTCCTGCCTCGGCCTCCCAAAG ATCGTGTTAGCCAGGATGGTCTCAATCTCCTGGCATTGTGATCCTCCTGCCTCGGCCTCCCAAAG T C PTGES3 Ensembl:ENSG00000110958 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1221084481 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11990716,Human_RBP_ID_24985570 RMVar_hsa_circ_73656,RMVar_hsa_circ_157454,RMVar_hsa_circ_95238 34051 RMVar_ID_34051 Human_SNP_ID_502470303 A-to-I Human chr12 - 56675498 56675498 56675498 TTTTTTTTTGGTCTCATTCTGTTGCCTAGGCTAGAGTGCAGTAGTGTGATCTTGGCTCACTGCAA TTTTTTTTTGGTCTCATTCTGTTGCCTAGGCTGGAGTGCAGTAGTGTGATCTTGGCTCACTGCAA T C PTGES3 Ensembl:ENSG00000110958 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs186624504 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11990745 RMVar_hsa_circ_73656,RMVar_hsa_circ_157454,RMVar_hsa_circ_95238 34052 RMVar_ID_34052 Human_SNP_ID_502470871 A-to-I Human chr12 - 56676883 56676883 56676883 GGAATCTCACTCTCTCACCCAGGCTGCAGTGCAGTGGCACGATCTCAGCTCACTGCAACCTCCAC GGAATCTCACTCTCTCACCCAGGCTGCAGTGCCGTGGCACGATCTCAGCTCACTGCAACCTCCAC T G PTGES3 Ensembl:ENSG00000110958 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs986300872 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11990821,Human_RBP_ID_24985606 RMVar_hsa_circ_73656,RMVar_hsa_circ_157454,RMVar_hsa_circ_95238 34053 RMVar_ID_34053 Human_SNP_ID_502471438 A-to-I Human chr12 - 56678356 56678356 56678356 CCTGGCCAACATGGTGAAAACCTGCCTCTACTAAAAAACAAAAATTAGCCAGGCTTGGTGGCGGG CCTGGCCAACATGGTGAAAACCTGCCTCTACTGAAAAACAAAAATTAGCCAGGCTTGGTGGCGGG T C PTGES3 Ensembl:ENSG00000110958 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1362342709 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11990900 RMVar_hsa_circ_73656,RMVar_hsa_circ_157454,RMVar_hsa_circ_95238 34054 RMVar_ID_34054 Human_SNP_ID_502471439 A-to-I Human chr12 - 56678359 56678359 56678359 CAGCCTGGCCAACATGGTGAAAACCTGCCTCTACTAAAAAACAAAAATTAGCCAGGCTTGGTGGC CAGCCTGGCCAACATGGTGAAAACCTGCCTCTGCTAAAAAACAAAAATTAGCCAGGCTTGGTGGC T C PTGES3 Ensembl:ENSG00000110958 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs888964207 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11990900 RMVar_hsa_circ_73656,RMVar_hsa_circ_157454,RMVar_hsa_circ_95238 34055 RMVar_ID_34055 Human_SNP_ID_502471676 A-to-I Human chr12 - 56679100 56679100 56679100 GTCTCCATGCTTCTCTAAGTCAGGGTCTTGCTATGTGGCCCAGGCTGGAGTGCAGTGGTACAACC GTCTCCATGCTTCTCTAAGTCAGGGTCTTGCTGTGTGGCCCAGGCTGGAGTGCAGTGGTACAACC T C PTGES3 Ensembl:ENSG00000110958 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027117922 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19789798,Human_RBP_ID_24985631 RMVar_hsa_circ_73656,RMVar_hsa_circ_157454,RMVar_hsa_circ_95238 34056 RMVar_ID_34056 Human_SNP_ID_502471677 A-to-I Human chr12 - 56679100 56679100 56679100 GTCTCCATGCTTCTCTAAGTCAGGGTCTTGCTATGTGGCCCAGGCTGGAGTGCAGTGGTACAACC GTCTCCATGCTTCTCTAAGTCAGGGTCTTGCTCTGTGGCCCAGGCTGGAGTGCAGTGGTACAACC T G PTGES3 Ensembl:ENSG00000110958 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027117922 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19789798,Human_RBP_ID_24985631 RMVar_hsa_circ_73656,RMVar_hsa_circ_157454,RMVar_hsa_circ_95238 34057 RMVar_ID_34057 Human_SNP_ID_502471708 A-to-I Human chr12 - 56679189 56679189 56679189 GGCATGGTTGGTTTGAACTCCTGGCCTCCAGTAATCTGCCAGCCTTGGGCTCCCAAAGTGCTGAT GGCATGGTTGGTTTGAACTCCTGGCCTCCAGTCATCTGCCAGCCTTGGGCTCCCAAAGTGCTGAT T G PTGES3 Ensembl:ENSG00000110958 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs568835915 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17561428 RMVar_hsa_circ_73656,RMVar_hsa_circ_157454,RMVar_hsa_circ_95238 34058 RMVar_ID_34058 Human_SNP_ID_502471720 A-to-I Human chr12 - 56679237 56679235 56679237 GCCCAACTAATTTTTGTATCTTCAGTAGAGACAGGGTTTTGCCATGTTGGCATGGTTGGTTTGAA GCCCAACTAATTTTTGTATCTTCAGTAGAGAC__GGTTTTGCCATGTTGGCATGGTTGGTTTGAA CCT C PTGES3 Ensembl:ENSG00000110958 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs895713276 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_6201925,Human_RBP_ID_11990940,Human_RBP_ID_17561428 RMVar_hsa_circ_73656,RMVar_hsa_circ_157454,RMVar_hsa_circ_95238 34059 RMVar_ID_34059 Human_SNP_ID_502471722 A-to-I Human chr12 - 56679246 56679246 56679246 TGCTACCATGCCCAACTAATTTTTGTATCTTCAGTAGAGACAGGGTTTTGCCATGTTGGCATGGT TGCTACCATGCCCAACTAATTTTTGTATCTTCGGTAGAGACAGGGTTTTGCCATGTTGGCATGGT T C PTGES3 Ensembl:ENSG00000110958 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1026095332 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6201925,Human_RBP_ID_11990941 RMVar_hsa_circ_73656,RMVar_hsa_circ_157454,RMVar_hsa_circ_95238 34060 RMVar_ID_34060 Human_SNP_ID_502471940 A-to-I Human chr12 - 56679737 56679737 56679737 CTGGGAGGTGGAGGTTGCGGTGAGCCAAGATCATGCCACCGTTCTCCAGCCTGTCACTCCGGGGT CTGGGAGGTGGAGGTTGCGGTGAGCCAAGATCGTGCCACCGTTCTCCAGCCTGTCACTCCGGGGT T C PTGES3 Ensembl:ENSG00000110958 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs551418026 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2345511,Human_RBP_ID_23158576 RMVar_hsa_circ_73656,RMVar_hsa_circ_157454,RMVar_hsa_circ_95238 34061 RMVar_ID_34061 Human_SNP_ID_502472185 A-to-I Human chr12 - 56680350 56680350 56680350 GAAAATTGGGTTGGGTGCAGTGACTCACACCTATAATCCCACCACTTTGGGGGACTGAGGTGGGC GAAAATTGGGTTGGGTGCAGTGACTCACACCTGTAATCCCACCACTTTGGGGGACTGAGGTGGGC T C PTGES3 Ensembl:ENSG00000110958 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1000051164 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17561165,Human_RBP_ID_24985658 RMVar_hsa_circ_73656,RMVar_hsa_circ_157454,RMVar_hsa_circ_95238 34062 RMVar_ID_34062 Human_SNP_ID_502472186 A-to-I Human chr12 - 56680354 56680352 56680354 GAAAGAAAATTGGGTTGGGTGCAGTGACTCACACCTATAATCCCACCACTTTGGGGGACTGAGGT GAAAGAAAATTGGGTTGGGTGCAGTGACTCAC__CTATAATCCCACCACTTTGGGGGACTGAGGT GGT G PTGES3 Ensembl:ENSG00000110958 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs988952213 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_17561165 RMVar_hsa_circ_73656,RMVar_hsa_circ_157454,RMVar_hsa_circ_95238 34063 RMVar_ID_34063 Human_SNP_ID_502472374 A-to-I Human chr12 - 56680813 56680813 56680813 GATCACGCCACAGCACTCCAGCCTGAATGACAAAGCAAGAACTGGTCTCAAAAAAAAAAAAAAAC GATCACGCCACAGCACTCCAGCCTGAATGACAGAGCAAGAACTGGTCTCAAAAAAAAAAAAAAAC T C PTGES3 Ensembl:ENSG00000110958 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs572510179 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8380304 RMVar_hsa_circ_73656,RMVar_hsa_circ_157454,RMVar_hsa_circ_95238 34064 RMVar_ID_34064 Human_SNP_ID_502472392 A-to-I Human chr12 - 56680866 56680866 56680866 GACTGAGGTGGGAGGATCACCTGAGCCTGCGAAGTCAAGGCTGTGTGAGCTGAGATCACGCCACA GACTGAGGTGGGAGGATCACCTGAGCCTGCGAGGTCAAGGCTGTGTGAGCTGAGATCACGCCACA T C PTGES3 Ensembl:ENSG00000110958 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335657815 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11990979,Human_RBP_ID_17560895 RMVar_hsa_circ_73656,RMVar_hsa_circ_157454,RMVar_hsa_circ_95238 34065 RMVar_ID_34065 Human_SNP_ID_502472722 A-to-I Human chr12 - 56681715 56681715 56681715 GAGTACCTGGGATTACAGGCGCATGCCACCGTACCTGGCTAATTTTTGTATTTTTTTTTTTAAGT GAGTACCTGGGATTACAGGCGCATGCCACCGTGCCTGGCTAATTTTTGTATTTTTTTTTTTAAGT T C PTGES3 Ensembl:ENSG00000110958 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1183695762 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73656,RMVar_hsa_circ_157454,RMVar_hsa_circ_95238 34066 RMVar_ID_34066 Human_SNP_ID_502472803 A-to-I Human chr12 - 56681939 56681939 56681939 GGGAGGCTGAGGCAGGAGAATGGTTTGAACCCAGGAGGCGAGGAGGTTGCAGTGAGCCGAGAATG GGGAGGCTGAGGCAGGAGAATGGTTTGAACCCGGGAGGCGAGGAGGTTGCAGTGAGCCGAGAATG T C PTGES3 Ensembl:ENSG00000110958 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1294726405 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73656,RMVar_hsa_circ_157454,RMVar_hsa_circ_95238 34067 RMVar_ID_34067 Human_SNP_ID_502472814 A-to-I Human chr12 - 56681979 56681979 56681979 AGCTGGGCACCGTGGCGGGTGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATGGTT AGCTGGGCACCGTGGCGGGTGCCTGTAATCCCGGCTACTTGGGAGGCTGAGGCAGGAGAATGGTT T C PTGES3 Ensembl:ENSG00000110958 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1191779436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22574717 RMVar_hsa_circ_73656,RMVar_hsa_circ_157454,RMVar_hsa_circ_95238 34068 RMVar_ID_34068 Human_SNP_ID_502473378 A-to-I Human chr12 - 56683390 56683390 56683390 CGGCTCACCGCAACCTCCGCCTCCTGTGTTCAAGCAATTCTCCTGCCTCAGCCTCCCGGGTAGCT CGGCTCACCGCAACCTCCGCCTCCTGTGTTCAGGCAATTCTCCTGCCTCAGCCTCCCGGGTAGCT T C PTGES3 Ensembl:ENSG00000110958 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs941431191 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73656,RMVar_hsa_circ_157454,RMVar_hsa_circ_95238 34069 RMVar_ID_34069 Human_SNP_ID_502473487 A-to-I Human chr12 - 56683551 56683551 56683551 CCGCCTTCTGGGTTGAAGTAGTTCTCTGCCTCAGCTTCCTGAGTAGCTGGGATTCCAGGTGCCTG CCGCCTTCTGGGTTGAAGTAGTTCTCTGCCTCTGCTTCCTGAGTAGCTGGGATTCCAGGTGCCTG T A PTGES3 Ensembl:ENSG00000110958 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1364834151 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11991076 RMVar_hsa_circ_73656,RMVar_hsa_circ_157454,RMVar_hsa_circ_95238 34070 RMVar_ID_34070 Human_SNP_ID_502473504 A-to-I Human chr12 - 56683587 56683587 56683587 GGAGTGAACTGGTGCGATCTCGGCTCACTGCAACCTCCGCCTTCTGGGTTGAAGTAGTTCTCTGC GGAGTGAACTGGTGCGATCTCGGCTCACTGCAGCCTCCGCCTTCTGGGTTGAAGTAGTTCTCTGC T C PTGES3 Ensembl:ENSG00000110958 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982811877 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2345525,Human_RBP_ID_11991076,Human_RBP_ID_23567345 RMVar_hsa_circ_73656,RMVar_hsa_circ_157454,RMVar_hsa_circ_95238 34071 RMVar_ID_34071 Human_SNP_ID_502473505 A-to-I Human chr12 - 56683587 56683587 56683587 GGAGTGAACTGGTGCGATCTCGGCTCACTGCAACCTCCGCCTTCTGGGTTGAAGTAGTTCTCTGC GGAGTGAACTGGTGCGATCTCGGCTCACTGCACCCTCCGCCTTCTGGGTTGAAGTAGTTCTCTGC T G PTGES3 Ensembl:ENSG00000110958 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982811877 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2345525,Human_RBP_ID_11991076,Human_RBP_ID_23567345 RMVar_hsa_circ_73656,RMVar_hsa_circ_157454,RMVar_hsa_circ_95238 34072 RMVar_ID_34072 Human_SNP_ID_502474076 A-to-I Human chr12 - 56684992 56684992 56684992 CTCAGTCTCCCGAGTAGCTGGGACTGCAGGCAAGCACCACCATGCCTGGCTAATAAATTTTTTTT CTCAGTCTCCCGAGTAGCTGGGACTGCAGGCAGGCACCACCATGCCTGGCTAATAAATTTTTTTT T C PTGES3 Ensembl:ENSG00000110958 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1307491045 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73656,RMVar_hsa_circ_157454,RMVar_hsa_circ_95238 34073 RMVar_ID_34073 Human_SNP_ID_502474110 A-to-I Human chr12 - 56685098 56685098 56685098 TAACTTGTTTTAAAAGTGTTTTTTTTGGAGACAGGGTCTTCCTCTGTCACCCAGGCTGGAGTGCA TAACTTGTTTTAAAAGTGTTTTTTTTGGAGACGGGGTCTTCCTCTGTCACCCAGGCTGGAGTGCA T C PTGES3 Ensembl:ENSG00000110958 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1051951509 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73656,RMVar_hsa_circ_157454,RMVar_hsa_circ_95238 34074 RMVar_ID_34074 Human_SNP_ID_502474332 A-to-I Human chr12 - 56685512 56685512 56685512 CCTGTGGTCCCAGCTACTTGGGAGGCTAAGGCAAGAGAATGGCTTGAACCCGGAAGGCGGAGCTT CCTGTGGTCCCAGCTACTTGGGAGGCTAAGGCGAGAGAATGGCTTGAACCCGGAAGGCGGAGCTT T C PTGES3 Ensembl:ENSG00000110958 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1055895401 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_113533,Human_RBP_ID_11991197,Human_RBP_ID_24985755 RMVar_hsa_circ_73656,RMVar_hsa_circ_157454,RMVar_hsa_circ_95238 34075 RMVar_ID_34075 Human_SNP_ID_502474333 A-to-I Human chr12 - 56685517 56685517 56685517 GGGCGCCTGTGGTCCCAGCTACTTGGGAGGCTAAGGCAAGAGAATGGCTTGAACCCGGAAGGCGG GGGCGCCTGTGGTCCCAGCTACTTGGGAGGCTGAGGCAAGAGAATGGCTTGAACCCGGAAGGCGG T C PTGES3 Ensembl:ENSG00000110958 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1349849111 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_113533 RMVar_hsa_circ_73656,RMVar_hsa_circ_157454,RMVar_hsa_circ_95238 34076 RMVar_ID_34076 Human_SNP_ID_502476267 A-to-I Human chr12 + 56690254 56690254 56690254 AGAATCTCTTGAACCCGGAAGACGCAGGTTGCAGCGAGTCTAGATTGTACCACTGTACTCCAGCT AGAATCTCTTGAACCCGGAAGACGCAGGTTGCGGCGAGTCTAGATTGTACCACTGTACTCCAGCT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1311149625 Functional Loss SNV dbSNP153 33..33 33 - - - 34077 RMVar_ID_34077 Human_SNP_ID_502487691 A-to-I Human chr12 - 56726856 56726856 56726856 GCTTAGAATATCCAAGAAGTGCCAGGGGCGGTAGTTCACGCCTGTAATCCCAGCACTTTGGGAGG GCTTAGAATATCCAAGAAGTGCCAGGGGCGGTGGTTCACGCCTGTAATCCCAGCACTTTGGGAGG T C NACA,AC117378.1 Ensembl:ENSG00000196531,Ensembl:ENSG00000285625 Protein coding,Protein coding 5'UTR,intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1393837305 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11991815,Human_RBP_ID_22906464 34078 RMVar_ID_34078 Human_SNP_ID_502488102 A-to-I Human chr12 - 56728373 56728373 56728373 GGGTGTGGTGTTGTGTGCCTGTAGTTCCAGCTACTCGGGAGGCTGAGGTGGGAGAATCGTTTATG GGGTGTGGTGTTGTGTGCCTGTAGTTCCAGCTGCTCGGGAGGCTGAGGTGGGAGAATCGTTTATG T C NACA,AC117378.1 Ensembl:ENSG00000196531,Ensembl:ENSG00000285625 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs779134239 Functional Loss SNV dbSNP153 33..33 33 - - - 34079 RMVar_ID_34079 Human_SNP_ID_502488303 A-to-I Human chr12 - 56729196 56729196 56729196 GCTAGAGTGCAGTGGCGCCATCTCGGCTCACTACAAACTCCACCTCCCAGGTTCGCGCCATTCTC GCTAGAGTGCAGTGGCGCCATCTCGGCTCACTGCAAACTCCACCTCCCAGGTTCGCGCCATTCTC T C NACA,AC117378.1 Ensembl:ENSG00000196531,Ensembl:ENSG00000285625 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1259200939 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25025282 34080 RMVar_ID_34080 Human_SNP_ID_502488410 A-to-I Human chr12 - 56729502 56729502 56729502 CCAGGCTGGTGTCGAACTCCTGAGCTTGGGCAATCCACCTGCCTTGGCCTCCCAGGTGTGAGCCA CCAGGCTGGTGTCGAACTCCTGAGCTTGGGCAGTCCACCTGCCTTGGCCTCCCAGGTGTGAGCCA T C NACA,AC117378.1 Ensembl:ENSG00000196531,Ensembl:ENSG00000285625 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1023708155 Functional Loss SNV dbSNP153 33..33 33 - - - 34081 RMVar_ID_34081 Human_SNP_ID_502488595 A-to-I Human chr12 - 56730446 56730446 56730446 AGAGAATCACCTGAACCCATGAGGTGGAGGTTACAGTGAGCTGAGATCACGCCACTGCACTCCAT AGAGAATCACCTGAACCCATGAGGTGGAGGTTGCAGTGAGCTGAGATCACGCCACTGCACTCCAT T C NACA,AC117378.1 Ensembl:ENSG00000196531,Ensembl:ENSG00000285625 Protein coding,Protein coding intron,intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1296019586 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3409675,Human_RBP_ID_11991856 34082 RMVar_ID_34082 Human_SNP_ID_502488601 A-to-I Human chr12 - 56730464 56730464 56730464 ACTAAGAAGGCTGAGGCAAGAGAATCACCTGAACCCATGAGGTGGAGGTTACAGTGAGCTGAGAT ACTAAGAAGGCTGAGGCAAGAGAATCACCTGAGCCCATGAGGTGGAGGTTACAGTGAGCTGAGAT T C NACA,AC117378.1 Ensembl:ENSG00000196531,Ensembl:ENSG00000285625 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965550339 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3409675,Human_RBP_ID_11991856,Human_RBP_ID_23158665 34083 RMVar_ID_34083 Human_SNP_ID_502488604 A-to-I Human chr12 - 56730478 56730478 56730478 CTGTAATCCCAGCTACTAAGAAGGCTGAGGCAAGAGAATCACCTGAACCCATGAGGTGGAGGTTA CTGTAATCCCAGCTACTAAGAAGGCTGAGGCAGGAGAATCACCTGAACCCATGAGGTGGAGGTTA T C NACA,AC117378.1 Ensembl:ENSG00000196531,Ensembl:ENSG00000285625 Protein coding,Protein coding intron,intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1330686982 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3409675,Human_RBP_ID_11991856 34084 RMVar_ID_34084 Human_SNP_ID_502488611 A-to-I Human chr12 - 56730493 56730493 56730493 TGTGGTGGCGGGCACCTGTAATCCCAGCTACTAAGAAGGCTGAGGCAAGAGAATCACCTGAACCC TGTGGTGGCGGGCACCTGTAATCCCAGCTACTGAGAAGGCTGAGGCAAGAGAATCACCTGAACCC T C NACA,AC117378.1 Ensembl:ENSG00000196531,Ensembl:ENSG00000285625 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1455642141 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4233812,Human_RBP_ID_11991856 34085 RMVar_ID_34085 Human_SNP_ID_502488613 A-to-I Human chr12 - 56730505 56730505 56730505 AAATTAGCCAGGTGTGGTGGCGGGCACCTGTAATCCCAGCTACTAAGAAGGCTGAGGCAAGAGAA AAATTAGCCAGGTGTGGTGGCGGGCACCTGTAGTCCCAGCTACTAAGAAGGCTGAGGCAAGAGAA T C NACA,AC117378.1 Ensembl:ENSG00000196531,Ensembl:ENSG00000285625 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1190856891 Functional Loss SNV dbSNP153 33..33 33 - - - 34086 RMVar_ID_34086 Human_SNP_ID_502488622 A-to-I Human chr12 - 56730528 56730528 56730528 CGGTCTCCACTAAAAATACAAGAAAATTAGCCAGGTGTGGTGGCGGGCACCTGTAATCCCAGCTA CGGTCTCCACTAAAAATACAAGAAAATTAGCCGGGTGTGGTGGCGGGCACCTGTAATCCCAGCTA T C NACA,AC117378.1 Ensembl:ENSG00000196531,Ensembl:ENSG00000285625 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs11830865 Functional Loss SNV dbSNP153 33..33 33 - - - 34087 RMVar_ID_34087 Human_SNP_ID_502488623 A-to-I Human chr12 - 56730532 56730532 56730532 AACCCGGTCTCCACTAAAAATACAAGAAAATTAGCCAGGTGTGGTGGCGGGCACCTGTAATCCCA AACCCGGTCTCCACTAAAAATACAAGAAAATTGGCCAGGTGTGGTGGCGGGCACCTGTAATCCCA T C NACA,AC117378.1 Ensembl:ENSG00000196531,Ensembl:ENSG00000285625 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1301309400 Functional Loss SNV dbSNP153 33..33 33 - - - 34088 RMVar_ID_34088 Human_SNP_ID_502488625 A-to-I Human chr12 - 56730540 56730540 56730540 CATGGTGAAACCCGGTCTCCACTAAAAATACAAGAAAATTAGCCAGGTGTGGTGGCGGGCACCTG CATGGTGAAACCCGGTCTCCACTAAAAATACAGGAAAATTAGCCAGGTGTGGTGGCGGGCACCTG T C NACA,AC117378.1 Ensembl:ENSG00000196531,Ensembl:ENSG00000285625 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs926924445 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26418404 34089 RMVar_ID_34089 Human_SNP_ID_502488632 A-to-I Human chr12 - 56730573 56730573 56730573 CTGAGGCCAGGAGTTCAAGGCCAGCCTGGCCAACATGGTGAAACCCGGTCTCCACTAAAAATACA CTGAGGCCAGGAGTTCAAGGCCAGCCTGGCCAGCATGGTGAAACCCGGTCTCCACTAAAAATACA T C NACA,AC117378.1 Ensembl:ENSG00000196531,Ensembl:ENSG00000285625 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs931545413 Functional Loss SNV dbSNP153 33..33 33 - - - 34090 RMVar_ID_34090 Human_SNP_ID_502488633 A-to-I Human chr12 - 56730574 56730574 56730574 ACTGAGGCCAGGAGTTCAAGGCCAGCCTGGCCAACATGGTGAAACCCGGTCTCCACTAAAAATAC ACTGAGGCCAGGAGTTCAAGGCCAGCCTGGCCGACATGGTGAAACCCGGTCTCCACTAAAAATAC T C NACA,AC117378.1 Ensembl:ENSG00000196531,Ensembl:ENSG00000285625 Protein coding,Protein coding intron,intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1048663560 Functional Loss SNV dbSNP153 33..33 33 - - - 34091 RMVar_ID_34091 Human_SNP_ID_502488648 A-to-I Human chr12 - 56730627 56730627 56730627 CCTGTCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCACACCCGACTGAGGCCAGG CCTGTCTCAGCCTCCCAAAGTGCTGGGATTACGGGTGTGAGCCACCACACCCGACTGAGGCCAGG T C NACA,AC117378.1 Ensembl:ENSG00000196531,Ensembl:ENSG00000285625 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1228557624 Functional Loss SNV dbSNP153 33..33 33 - - - 34092 RMVar_ID_34092 Human_SNP_ID_502488649 A-to-I Human chr12 - 56730641 56730641 56730641 GACCTTGTGATCTGCCTGTCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCACACC GACCTTGTGATCTGCCTGTCTCAGCCTCCCAAGGTGCTGGGATTACAGGTGTGAGCCACCACACC T C NACA,AC117378.1 Ensembl:ENSG00000196531,Ensembl:ENSG00000285625 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1019745714 Functional Loss SNV dbSNP153 33..33 33 - - - 34093 RMVar_ID_34093 Human_SNP_ID_502488653 A-to-I Human chr12 - 56730651 56730651 56730651 TCGATCTCCTGACCTTGTGATCTGCCTGTCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG TCGATCTCCTGACCTTGTGATCTGCCTGTCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG T C NACA,AC117378.1 Ensembl:ENSG00000196531,Ensembl:ENSG00000285625 Protein coding,Protein coding intron,intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1476327032 Functional Loss SNV dbSNP153 33..33 33 - - - 34094 RMVar_ID_34094 Human_SNP_ID_502488686 A-to-I Human chr12 - 56730775 56730775 56730775 TCATGCCATTCTCCTGCCTCAGCCTCCCAAATAGCTGAGACTACAGGTGCCCGCCACCACGCCCA TCATGCCATTCTCCTGCCTCAGCCTCCCAAATGGCTGAGACTACAGGTGCCCGCCACCACGCCCA T C NACA,AC117378.1 Ensembl:ENSG00000196531,Ensembl:ENSG00000285625 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1386798991 Functional Loss SNV dbSNP153 33..33 33 - - - 34095 RMVar_ID_34095 Human_SNP_ID_502488746 A-to-I Human chr12 - 56730955 56730955 56730955 GCCAGGCACAGTGGCTCATACCTGTAATCCCAACACTTTGGGAGGCCAAGACAGGCAGATCACCT GCCAGGCACAGTGGCTCATACCTGTAATCCCAGCACTTTGGGAGGCCAAGACAGGCAGATCACCT T C NACA,AC117378.1 Ensembl:ENSG00000196531,Ensembl:ENSG00000285625 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1482053934 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23158668 34096 RMVar_ID_34096 Human_SNP_ID_502488810 A-to-I Human chr12 - 56731285 56731285 56731285 CCACTGGGCGACAGAGCGAGACTCCATCTCAAAAAAGAAACAAAACAAAAAAAAAAGTAAGATTT CCACTGGGCGACAGAGCGAGACTCCATCTCAACAAAGAAACAAAACAAAAAAAAAAGTAAGATTT T G NACA,AC117378.1 Ensembl:ENSG00000196531,Ensembl:ENSG00000285625 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904276888 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25025283,Human_RBP_ID_26418407 RMVar_hsa_circ_157473 34097 RMVar_ID_34097 Human_SNP_ID_502488811 A-to-I Human chr12 - 56731292 56731292 56731292 ATCACAGCCACTGGGCGACAGAGCGAGACTCCATCTCAAAAAAGAAACAAAACAAAAAAAAAAGT ATCACAGCCACTGGGCGACAGAGCGAGACTCCGTCTCAAAAAAGAAACAAAACAAAAAAAAAAGT T C NACA,AC117378.1 Ensembl:ENSG00000196531,Ensembl:ENSG00000285625 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404528615 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6202185,Human_RBP_ID_25025283,Human_RBP_ID_26418407 RMVar_hsa_circ_157473 34098 RMVar_ID_34098 Human_SNP_ID_502488825 A-to-I Human chr12 - 56731348 56731348 56731348 AGGCTGAGGCAGGAGAATTGCTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCTGAGATCACAGCC AGGCTGAGGCAGGAGAATTGCTTGAACCCAGGGGGCAGAGGTTGCAGTGAGCTGAGATCACAGCC T C PRIM1,NACA,AC117378.1 Ensembl:ENSG00000198056,Ensembl:ENSG00000196531,Ensembl:ENSG00000285625 Protein coding,Protein coding,Protein coding 3'UTR,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277406887 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_157473 34099 RMVar_ID_34099 Human_SNP_ID_502488827 A-to-I 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 GSE38233;GSE100210;GSE112787;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;293 Flip-In T-REx cells,empty vector;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,29967493,31158229,31158229,31158229 RNA-Seq:(High) rs1206430213 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_157473 34100 RMVar_ID_34100 Human_SNP_ID_502488829 A-to-I 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 GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1024674689 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_157473 34101 RMVar_ID_34101 Human_SNP_ID_502488834 A-to-I Human chr12 - 56731396 56731396 56731396 AAAATCAGTCGGGTGTGGTGGTGCATACAGTAATCCTAGCTACTTGGGAGGCTGAGGCAGGAGAA AAAATCAGTCGGGTGTGGTGGTGCATACAGTAGTCCTAGCTACTTGGGAGGCTGAGGCAGGAGAA T C PRIM1,NACA,AC117378.1 Ensembl:ENSG00000198056,Ensembl:ENSG00000196531,Ensembl:ENSG00000285625 Protein coding,Protein coding,Protein coding 3'UTR,intron,intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1002161109 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1798047 RMVar_hsa_circ_157473 34102 RMVar_ID_34102 Human_SNP_ID_502488835 A-to-I Human chr12 - 56731397 56731397 56731397 AAAAATCAGTCGGGTGTGGTGGTGCATACAGTAATCCTAGCTACTTGGGAGGCTGAGGCAGGAGA AAAAATCAGTCGGGTGTGGTGGTGCATACAGTGATCCTAGCTACTTGGGAGGCTGAGGCAGGAGA T C PRIM1,NACA,AC117378.1 Ensembl:ENSG00000198056,Ensembl:ENSG00000196531,Ensembl:ENSG00000285625 Protein coding,Protein coding,Protein coding 3'UTR,intron,intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs1033699353 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1798047 RMVar_hsa_circ_157473 34103 RMVar_ID_34103 Human_SNP_ID_502488858 A-to-I Human chr12 - 56731460 56731460 56731460 GAGGTCAGTAGTTCGAGACTAGCCTGGCCAACATGGTGAAACCCCCGTCTCTACTAAAACTACAA GAGGTCAGTAGTTCGAGACTAGCCTGGCCAACGTGGTGAAACCCCCGTCTCTACTAAAACTACAA T C PRIM1,NACA,AC117378.1 Ensembl:ENSG00000198056,Ensembl:ENSG00000196531,Ensembl:ENSG00000285625 Protein coding,Protein coding,Protein coding 3'UTR,intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs923011624 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_157473 34104 RMVar_ID_34104 Human_SNP_ID_502488859 A-to-I Human chr12 - 56731463 56731463 56731463 CCTGAGGTCAGTAGTTCGAGACTAGCCTGGCCAACATGGTGAAACCCCCGTCTCTACTAAAACTA CCTGAGGTCAGTAGTTCGAGACTAGCCTGGCCGACATGGTGAAACCCCCGTCTCTACTAAAACTA T C PRIM1,NACA,AC117378.1 Ensembl:ENSG00000198056,Ensembl:ENSG00000196531,Ensembl:ENSG00000285625 Protein coding,Protein coding,Protein coding 3'UTR,intron,intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs1313371316 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_157473 34105 RMVar_ID_34105 Human_SNP_ID_502488863 A-to-I Human chr12 - 56731486 56731486 56731486 GGGAGGCCGAGGCAGGCGGATCACCTGAGGTCAGTAGTTCGAGACTAGCCTGGCCAACATGGTGA GGGAGGCCGAGGCAGGCGGATCACCTGAGGTCGGTAGTTCGAGACTAGCCTGGCCAACATGGTGA T C PRIM1,NACA,AC117378.1 Ensembl:ENSG00000198056,Ensembl:ENSG00000196531,Ensembl:ENSG00000285625 Protein coding,Protein coding,Protein coding 3'UTR,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1343443328 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_157473 34106 RMVar_ID_34106 Human_SNP_ID_502488878 A-to-I Human chr12 - 56731538 56731538 56731538 AAAAGATTTCCTGGCCAAGTGCAGTGGCTCACACCCGTAATCCCAGCACTTTGGGAGGCCGAGGC AAAAGATTTCCTGGCCAAGTGCAGTGGCTCACGCCCGTAATCCCAGCACTTTGGGAGGCCGAGGC T C PRIM1,NACA,AC117378.1 Ensembl:ENSG00000198056,Ensembl:ENSG00000196531,Ensembl:ENSG00000285625 Protein coding,Protein coding,Protein coding 3'UTR,5'UTR,intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1049441723 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26421420 Human_Splice_Rec_1385465 RMVar_hsa_circ_157473 34107 RMVar_ID_34107 Human_SNP_ID_502490987 A-to-I Human chr12 - 56740053 56740053 56740053 TGGCTCACTGCAGCCTCTGCCTTCCAGGTTCAAGCAATTCTCTGCCTCACCCTCCCAAGTAGCTG TGGCTCACTGCAGCCTCTGCCTTCCAGGTTCATGCAATTCTCTGCCTCACCCTCCCAAGTAGCTG T A PRIM1,AC117378.1 Ensembl:ENSG00000198056,Ensembl:ENSG00000285625 Protein coding,Protein coding CDS,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1293571152 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1385520,Human_Splice_Rec_1385521 RMVar_hsa_circ_850,RMVar_hsa_circ_285150,RMVar_hsa_circ_157474,RMVar_hsa_circ_87692,RMVar_hsa_circ_353960,RMVar_hsa_circ_362223,RMVar_hsa_circ_311745,RMVar_hsa_circ_157476,RMVar_hsa_circ_50478,RMVar_hsa_circ_278188,RMVar_hsa_circ_157478,RMVar_hsa_circ_157479,RMVar_hsa_circ_157477,RMVar_hsa_circ_333957,RMVar_hsa_circ_348466,RMVar_hsa_circ_313927,RMVar_hsa_circ_82695,RMVar_hsa_circ_157482,RMVar_hsa_circ_157483,RMVar_hsa_circ_157481,RMVar_hsa_circ_368629,RMVar_hsa_circ_378689,RMVar_hsa_circ_288198 34108 RMVar_ID_34108 Human_SNP_ID_502497154 A-to-I Human chr12 + 56765772 56765772 56765772 CAAGGAATTCGCCTACCTCAGCCTTCTAAAGTATTGGGATTACAAGTGTGAGCCACTGTGCCCAG CAAGGAATTCGCCTACCTCAGCCTTCTAAAGTGTTGGGATTACAAGTGTGAGCCACTGTGCCCAG A G HSD17B6 Ensembl:ENSG00000025423 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1367323859 Functional Loss SNV dbSNP153 33..33 33 - - - 34109 RMVar_ID_34109 Human_SNP_ID_502571214 A-to-I Human chr12 - 57056798 57056798 57056798 TGGTGTTCCCTTTAACCCTTGGCATGTATAATAGAATTTTGGTGAATGAAAGAACCCAAATAGGC TGGTGTTCCCTTTAACCCTTGGCATGTATAATGGAATTTTGGTGAATGAAAGAACCCAAATAGGC T C NEMP1 Ensembl:ENSG00000166881 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1332712718 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6202449,Human_RBP_ID_8380427,Human_RBP_ID_11992286,Human_RBP_ID_22794880,Human_RBP_ID_22906488,Human_RBP_ID_23567589,Human_RBP_ID_27631294 34110 RMVar_ID_34110 Human_SNP_ID_502574048 A-to-I Human chr12 - 57068043 57068043 57068043 TGGGGGGCTGGTTGTGGTGGCTCACCCCTGTAATCCTAGCACTTTGGGAGGCTGAAGGGGGAGGA TGGGGGGCTGGTTGTGGTGGCTCACCCCTGTATTCCTAGCACTTTGGGAGGCTGAAGGGGGAGGA T A NEMP1 Ensembl:ENSG00000166881 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs992926766 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_339917,RMVar_hsa_circ_157493,RMVar_hsa_circ_378982,RMVar_hsa_circ_60700,RMVar_hsa_circ_361937 34111 RMVar_ID_34111 Human_SNP_ID_502574162 A-to-I Human chr12 - 57068467 57068467 57068467 ATGTGCCTGTGATCCCAGTTACTCGAGAGGCTAAGGCACGAGAACCGCTTGAGCCTGGAGGCGGA ATGTGCCTGTGATCCCAGTTACTCGAGAGGCTGAGGCACGAGAACCGCTTGAGCCTGGAGGCGGA T C NEMP1 Ensembl:ENSG00000166881 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs747890734 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11992716,Human_RBP_ID_24986416 RMVar_hsa_circ_339917,RMVar_hsa_circ_157493,RMVar_hsa_circ_378982,RMVar_hsa_circ_60700,RMVar_hsa_circ_361937 34112 RMVar_ID_34112 Human_SNP_ID_502575422 A-to-I Human chr12 - 57073561 57073561 57073561 CGGCTCACCTCAACCTCCGCCTCCCAAGTTCAAGTGATTCTCCTGCCTCAGCCTCTCGAGTAGCT CGGCTCACCTCAACCTCCGCCTCCCAAGTTCAGGTGATTCTCCTGCCTCAGCCTCTCGAGTAGCT T C NEMP1 Ensembl:ENSG00000166881 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1047697526 Functional Loss SNV dbSNP153 33..33 33 - - - 34113 RMVar_ID_34113 Human_SNP_ID_502575543 A-to-I Human chr12 - 57074044 57074044 57074044 GGATTGTTTGAGCCCAAGAGTTTGAGGCTGCAATGAGCTATGATCACATTACTGTACTCCAGCCT GGATTGTTTGAGCCCAAGAGTTTGAGGCTGCAGTGAGCTATGATCACATTACTGTACTCCAGCCT T C NEMP1 Ensembl:ENSG00000166881 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs540390848 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6202667 34114 RMVar_ID_34114 Human_SNP_ID_502575558 A-to-I Human chr12 - 57074107 57074107 57074107 AAAACTAGCTGGGTGTGGTGGTGTATACCTGTAGTCCTGGCTACTTGGGAGGCTGAAGTGGGAGG AAAACTAGCTGGGTGTGGTGGTGTATACCTGTGGTCCTGGCTACTTGGGAGGCTGAAGTGGGAGG T C NEMP1 Ensembl:ENSG00000166881 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1193526990 Functional Loss SNV dbSNP153 33..33 33 - - - 34115 RMVar_ID_34115 Human_SNP_ID_502618479 A-to-I Human chr12 - 57229048 57229048 57229048 CCCCTCCTGTTGTTCACTTGTCCCATTTTGTTACCTGTCCACCTCTTGATGTCCCAGGAGTCGGT CCCCTCCTGTTGTTCACTTGTCCCATTTTGTTTCCTGTCCACCTCTTGATGTCCCAGGAGTCGGT T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs902785367 Functional Loss SNV dbSNP153 33..33 33 - - - 34116 RMVar_ID_34116 Human_SNP_ID_502626139 A-to-I Human chr12 - 57254379 57254379 57254379 CTCCTGCCTCAGCCTCCCAAGTAGCTGGCACTACAGACACGCGCCACCATGCCCGGCTAATTTTT CTCCTGCCTCAGCCTCCCAAGTAGCTGGCACTGCAGACACGCGCCACCATGCCCGGCTAATTTTT T C AC137834.1,R3HDM2 Ensembl:ENSG00000258830,Ensembl:ENSG00000179912 Protein coding,Protein coding intron,exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1166614952 Functional Loss SNV dbSNP153 33..33 33 - - - 34117 RMVar_ID_34117 Human_SNP_ID_502641198 A-to-I Human chr12 - 57322130 57322130 57322130 CTCACTGCAACCTCCGCCTCCAGGATTCAAGCAGTTCTGCTGCCTCAGCCTCCCGAACAGGCGAG CTCACTGCAACCTCCGCCTCCAGGATTCAAGCTGTTCTGCTGCCTCAGCCTCCCGAACAGGCGAG T A R3HDM2 Ensembl:ENSG00000179912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs980629474 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_424695 RMVar_hsa_circ_344725,RMVar_hsa_circ_157637,RMVar_hsa_circ_110776,RMVar_hsa_circ_157643,RMVar_hsa_circ_70804,RMVar_hsa_circ_38581,RMVar_hsa_circ_313248 34118 RMVar_ID_34118 Human_SNP_ID_502641950 A-to-I Human chr12 - 57325696 57325696 57325696 CAAAAAAAAAAAAAAAATTAGCTAAGGATAGTAGTGCATGCCTGTGGTTCCAGCAATTTGGGAGG CAAAAAAAAAAAAAAAATTAGCTAAGGATAGTGGTGCATGCCTGTGGTTCCAGCAATTTGGGAGG T C R3HDM2 Ensembl:ENSG00000179912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs549691952 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_344725,RMVar_hsa_circ_157637,RMVar_hsa_circ_110776,RMVar_hsa_circ_157643,RMVar_hsa_circ_70804,RMVar_hsa_circ_38581,RMVar_hsa_circ_313248 34119 RMVar_ID_34119 Human_SNP_ID_502643149 A-to-I Human chr12 - 57330827 57330827 57330827 GGGCGTGGTGGCGGGTGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATGGCGTGAA GGGCGTGGTGGCGGGTGCCTGTAGTCCCAGCTGCTTGGGAGGCTGAGGCAGGAGAATGGCGTGAA T C R3HDM2 Ensembl:ENSG00000179912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1314790043 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_344725,RMVar_hsa_circ_157637,RMVar_hsa_circ_110776,RMVar_hsa_circ_157643,RMVar_hsa_circ_70804,RMVar_hsa_circ_38581,RMVar_hsa_circ_313248 34120 RMVar_ID_34120 Human_SNP_ID_502643851 A-to-I Human chr12 - 57333853 57333853 57333853 TATTTTTAGTAGAGATGGGGTTTCGCCACGTTAGCCAGGCTGGTCTCGAACTCCTAACCTCGTCA TATTTTTAGTAGAGATGGGGTTTCGCCACGTTGGCCAGGCTGGTCTCGAACTCCTAACCTCGTCA T C R3HDM2 Ensembl:ENSG00000179912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1479560525 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_344725,RMVar_hsa_circ_157637,RMVar_hsa_circ_110776,RMVar_hsa_circ_157643,RMVar_hsa_circ_70804,RMVar_hsa_circ_38581,RMVar_hsa_circ_313248 34121 RMVar_ID_34121 Human_SNP_ID_502649477 A-to-I Human chr12 - 57358099 57358099 57358099 CGTCACGCGCCTGTAGTCCCAGCTACTTGGGAAGCTGAGGCAGGAGAATTGCTTGAATCTGGGAG CGTCACGCGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATTGCTTGAATCTGGGAG T C R3HDM2 Ensembl:ENSG00000179912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs996895851 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_344725,RMVar_hsa_circ_157637,RMVar_hsa_circ_110776,RMVar_hsa_circ_157643,RMVar_hsa_circ_70804,RMVar_hsa_circ_38581,RMVar_hsa_circ_313248 34122 RMVar_ID_34122 Human_SNP_ID_502650261 A-to-I Human chr12 - 57360810 57360810 57360810 ACCTCATGACCCGCCCGCCTCAGCCTCCCAAAATGCTGGGATTACAGGCGTGAGCCACTGCGCCC ACCTCATGACCCGCCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCGCCC T C R3HDM2 Ensembl:ENSG00000179912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1309641580 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_344725,RMVar_hsa_circ_157637,RMVar_hsa_circ_110776,RMVar_hsa_circ_157643,RMVar_hsa_circ_70804,RMVar_hsa_circ_38581,RMVar_hsa_circ_313248 34123 RMVar_ID_34123 Human_SNP_ID_502650623 A-to-I Human chr12 - 57362021 57362021 57362021 CTCAAGCAATCCTCCCACCTCAGCCTCCGAGTAGCTGGGACTGCAGGCCTGCTCCACCGCGCATG CTCAAGCAATCCTCCCACCTCAGCCTCCGAGTGGCTGGGACTGCAGGCCTGCTCCACCGCGCATG T C R3HDM2 Ensembl:ENSG00000179912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs979421533 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_344725,RMVar_hsa_circ_157637,RMVar_hsa_circ_110776,RMVar_hsa_circ_157643,RMVar_hsa_circ_70804,RMVar_hsa_circ_38581,RMVar_hsa_circ_313248 34124 RMVar_ID_34124 Human_SNP_ID_502651008 A-to-I Human chr12 - 57363844 57363844 57363844 TTTTTTTTTAAGAGATGGAGTCTTGGTTGCCCAGGCTGGAGCACAGTGGTGTGATCCTAGCTCAC TTTTTTTTTAAGAGATGGAGTCTTGGTTGCCCCGGCTGGAGCACAGTGGTGTGATCCTAGCTCAC T G R3HDM2 Ensembl:ENSG00000179912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1424228971 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_344725,RMVar_hsa_circ_157637,RMVar_hsa_circ_110776,RMVar_hsa_circ_157643,RMVar_hsa_circ_70804,RMVar_hsa_circ_38581,RMVar_hsa_circ_313248 34125 RMVar_ID_34125 Human_SNP_ID_502654127 A-to-I Human chr12 - 57375810 57375810 57375810 ATATTAGCTGCACATGGTGGTGTGGGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCGGGAGAA ATATTAGCTGCACATGGTGGTGTGGGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCGGGAGAA T C R3HDM2 Ensembl:ENSG00000179912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs529826417 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_344725,RMVar_hsa_circ_157637,RMVar_hsa_circ_110776,RMVar_hsa_circ_157643,RMVar_hsa_circ_70804,RMVar_hsa_circ_38581,RMVar_hsa_circ_313248 34126 RMVar_ID_34126 Human_SNP_ID_502654737 A-to-I Human chr12 - 57378606 57378606 57378606 GGGAGGCCAAAGCAGAAGGATGTCTTGAGTCCAGGAGTTTGAGACCAGCCTGGGCAACATGGCAA GGGAGGCCAAAGCAGAAGGATGTCTTGAGTCCGGGAGTTTGAGACCAGCCTGGGCAACATGGCAA T C R3HDM2 Ensembl:ENSG00000179912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1254682150 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_344725,RMVar_hsa_circ_157637,RMVar_hsa_circ_110776,RMVar_hsa_circ_157643,RMVar_hsa_circ_70804,RMVar_hsa_circ_38581,RMVar_hsa_circ_313248 34127 RMVar_ID_34127 Human_SNP_ID_502656242 A-to-I Human chr12 - 57384955 57384955 57384955 TTTAGTAGAGATGGGGTTTCACCGTTTTGGCCAGGCTGGTCTTGAACTCCTGACCTCGTGATCCA TTTAGTAGAGATGGGGTTTCACCGTTTTGGCCCGGCTGGTCTTGAACTCCTGACCTCGTGATCCA T G R3HDM2 Ensembl:ENSG00000179912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982526744 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_344725,RMVar_hsa_circ_157637,RMVar_hsa_circ_110776,RMVar_hsa_circ_157643,RMVar_hsa_circ_70804,RMVar_hsa_circ_38581,RMVar_hsa_circ_313248 34128 RMVar_ID_34128 Human_SNP_ID_502659723 A-to-I Human chr12 - 57398518 57398518 57398518 CGCCACTGCACTCCAGCCTGTGTGACGGAGTAAGACTCCATCTCAAAAAAAAAAAAGAGAGAGAA CGCCACTGCACTCCAGCCTGTGTGACGGAGTAGGACTCCATCTCAAAAAAAAAAAAGAGAGAGAA T C R3HDM2 Ensembl:ENSG00000179912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs967462357 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93739,RMVar_hsa_circ_157649 34129 RMVar_ID_34129 Human_SNP_ID_502659763 A-to-I Human chr12 - 57398662 57398662 57398662 TAACATGGTGAAACTTTGTCGGTACTAAAAATACAAAAATTAGCCGGGCATGGTGGCGGGCACCT TAACATGGTGAAACTTTGTCGGTACTAAAAATGCAAAAATTAGCCGGGCATGGTGGCGGGCACCT T C R3HDM2 Ensembl:ENSG00000179912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1050106600 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93739,RMVar_hsa_circ_157649 34130 RMVar_ID_34130 Human_SNP_ID_502661319 A-to-I Human chr12 - 57405104 57405104 57405104 AAGATTACTCGAGCCCAGGAGGTTGAGGTTACAGTGAGCTATGATCATGTCACTGTACTCTAGCT AAGATTACTCGAGCCCAGGAGGTTGAGGTTACGGTGAGCTATGATCATGTCACTGTACTCTAGCT T C R3HDM2 Ensembl:ENSG00000179912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1466151045 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93739,RMVar_hsa_circ_157649 34131 RMVar_ID_34131 Human_SNP_ID_502661942 A-to-I Human chr12 - 57407904 57407904 57407904 AAAATTAGCTGGATGTGGTGGCACGCACCTGTAGTCCCCAGCTATGTGGGAGGCTGAGCTGAGAG AAAATTAGCTGGATGTGGTGGCACGCACCTGTGGTCCCCAGCTATGTGGGAGGCTGAGCTGAGAG T C R3HDM2 Ensembl:ENSG00000179912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs551376856 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93739,RMVar_hsa_circ_157649 34132 RMVar_ID_34132 Human_SNP_ID_502662930 A-to-I Human chr12 - 57412345 57412345 57412345 TAGGGACAAGGTTTCACAATGTTGGTCAGGCTAGTCTTGAACTCCTGATCTCAAGTGATTCGCCC TAGGGACAAGGTTTCACAATGTTGGTCAGGCTGGTCTTGAACTCCTGATCTCAAGTGATTCGCCC T C R3HDM2 Ensembl:ENSG00000179912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992473859 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93739,RMVar_hsa_circ_157649 34133 RMVar_ID_34133 Human_SNP_ID_502663162 A-to-I Human chr12 - 57413331 57413331 57413331 CCTCAGCATCCCAAAGTGTTGGGAGTACAGACATGAGCTACCATGCCTAGCCTTAACCTGAATTA CCTCAGCATCCCAAAGTGTTGGGAGTACAGACGTGAGCTACCATGCCTAGCCTTAACCTGAATTA T C R3HDM2 Ensembl:ENSG00000179912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs540730 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_3661,GWAS_ID_3662,GWAS_ID_3663,GWAS_ID_3664,GWAS_ID_3665,GWAS_ID_3666,GWAS_ID_3667,GWAS_ID_3668,GWAS_ID_3669,GWAS_ID_3670 RMVar_hsa_circ_93739,RMVar_hsa_circ_157649 34134 RMVar_ID_34134 Human_SNP_ID_502663273 A-to-I Human chr12 - 57413732 57413732 57413732 TTGTTGTTGTTGTTGTTGTTTTTTCCTTGAGAATGGAGTCTTGCTCTGTCACCCAGGCTGGAGTA TTGTTGTTGTTGTTGTTGTTTTTTCCTTGAGAGTGGAGTCTTGCTCTGTCACCCAGGCTGGAGTA T C R3HDM2 Ensembl:ENSG00000179912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs190555928 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2345819,Human_RBP_ID_3409900,Human_RBP_ID_6203333,Human_RBP_ID_23567985 RMVar_hsa_circ_93739,RMVar_hsa_circ_157649 34135 RMVar_ID_34135 Human_SNP_ID_502664080 A-to-I Human chr12 - 57416756 57416756 57416756 TTGCCCAGGCTGGAGTGCAGTGGCGCAGTCTCAGCTCACTGCAACCTCCGCCTCTCAGATTCAAG TTGCCCAGGCTGGAGTGCAGTGGCGCAGTCTCGGCTCACTGCAACCTCCGCCTCTCAGATTCAAG T C R3HDM2 Ensembl:ENSG00000179912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1175659641 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93739,RMVar_hsa_circ_157649 34136 RMVar_ID_34136 Human_SNP_ID_502664563 A-to-I Human chr12 - 57418619 57418619 57418619 GGGAGACAGAGGTTGCGGTGAGCTGAGATCGCACCACTGTACTCCAGCCTGGACGACAGAGACTC GGGAGACAGAGGTTGCGGTGAGCTGAGATCGCGCCACTGTACTCCAGCCTGGACGACAGAGACTC T C R3HDM2 Ensembl:ENSG00000179912 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1485358732 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24987710 RMVar_hsa_circ_93739,RMVar_hsa_circ_157649 34137 RMVar_ID_34137 Human_SNP_ID_502664568 A-to-I Human chr12 - 57418626 57418626 57418626 TGAACCGGGGAGACAGAGGTTGCGGTGAGCTGAGATCGCACCACTGTACTCCAGCCTGGACGACA TGAACCGGGGAGACAGAGGTTGCGGTGAGCTGCGATCGCACCACTGTACTCCAGCCTGGACGACA T G R3HDM2 Ensembl:ENSG00000179912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049089913 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93739,RMVar_hsa_circ_157649 34138 RMVar_ID_34138 Human_SNP_ID_502665060 A-to-I Human chr12 - 57420644 57420644 57420644 AGATAGATGGAAAACTAGTAAAGCCTGGGCGCAGTGGCTCACGCCCGTAATCCCAATACTATGGG AGATAGATGGAAAACTAGTAAAGCCTGGGCGCGGTGGCTCACGCCCGTAATCCCAATACTATGGG T C R3HDM2 Ensembl:ENSG00000179912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs187700049 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93739,RMVar_hsa_circ_157649 34139 RMVar_ID_34139 Human_SNP_ID_502665361 A-to-I Human chr12 - 57421781 57421781 57421781 AATAGATAGGCTGGGTGTAGTGTCTCACACCTATAATCCAGCACTTTGGGAGGCTGAGGTGGGAG AATAGATAGGCTGGGTGTAGTGTCTCACACCTGTAATCCAGCACTTTGGGAGGCTGAGGTGGGAG T C R3HDM2 Ensembl:ENSG00000179912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs557445701 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17561174,Human_RBP_ID_24987752 RMVar_hsa_circ_93739,RMVar_hsa_circ_157649 34140 RMVar_ID_34140 Human_SNP_ID_502665849 A-to-I Human chr12 - 57423664 57423664 57423664 GGGATTACAGGTGCCCGCCACCACGTCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCA GGGATTACAGGTGCCCGCCACCACGTCTGGCTGATTTTTGTATTTTTAGTAGAGATGGGGTTTCA T C R3HDM2 Ensembl:ENSG00000179912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1390014561 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93739,RMVar_hsa_circ_157649 34141 RMVar_ID_34141 Human_SNP_ID_502666084 A-to-I Human chr12 - 57424309 57424306 57424310 AAAAATACAAGACCTTAGCTGGGTGTTATGGTATCACATGCCTGTAATCCCAGCTACTCGGGAGG AAAAATACAAGACCTTAGCTGGGTGTTATGG____ACATGCCTGTAATCCCAGCTACTCGGGAGG TGATA T R3HDM2 Ensembl:ENSG00000179912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1555320681 Functional Loss DEL dbSNP153 32..35 33 - - - RMVar_hsa_circ_93739,RMVar_hsa_circ_157649 34142 RMVar_ID_34142 Human_SNP_ID_502666212 A-to-I Human chr12 - 57424848 57424848 57424848 AAATATTGTATAGGCTTGGCTTGGTGGTTCATACCTGTAGTGCAGCACTTTGGGAATCTGAGGCG AAATATTGTATAGGCTTGGCTTGGTGGTTCATTCCTGTAGTGCAGCACTTTGGGAATCTGAGGCG T A R3HDM2 Ensembl:ENSG00000179912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1343828451 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1942787,Human_miRNA_ID_1945833,Human_miRNA_ID_2116978,Human_miRNA_ID_2200556,Human_miRNA_ID_2203620,Human_miRNA_ID_2316097,Human_miRNA_ID_2319252,Human_miRNA_ID_2322412,Human_miRNA_ID_2325579,Human_miRNA_ID_2519956,Human_miRNA_ID_2523122,Human_miRNA_ID_2774963,Human_miRNA_ID_2816081,Human_miRNA_ID_2822316,Human_miRNA_ID_2828445,Human_miRNA_ID_2831603,Human_miRNA_ID_2835722,Human_miRNA_ID_2841077,Human_miRNA_ID_2846196,Human_miRNA_ID_2849221,Human_miRNA_ID_2863344,Human_miRNA_ID_3113073 RMVar_hsa_circ_93739,RMVar_hsa_circ_157649 34143 RMVar_ID_34143 Human_SNP_ID_502666536 A-to-I Human chr12 - 57425965 57425965 57425965 CCTCGGCCTCCCGAAGTGCTGGGATTACAGGCATGAGCCACCGCGCCTGACCTATCTTTCCTTAG CCTCGGCCTCCCGAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCCTGACCTATCTTTCCTTAG T C R3HDM2 Ensembl:ENSG00000179912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1410022836 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23158822 RMVar_hsa_circ_93739,RMVar_hsa_circ_157649 34144 RMVar_ID_34144 Human_SNP_ID_502666539 A-to-I Human chr12 - 57425971 57425971 57425971 TGCCCGCCTCGGCCTCCCGAAGTGCTGGGATTACAGGCATGAGCCACCGCGCCTGACCTATCTTT TGCCCGCCTCGGCCTCCCGAAGTGCTGGGATTCCAGGCATGAGCCACCGCGCCTGACCTATCTTT T G R3HDM2 Ensembl:ENSG00000179912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs545389238 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93739,RMVar_hsa_circ_157649 34145 RMVar_ID_34145 Human_SNP_ID_502667201 A-to-I Human chr12 - 57428373 57428373 57428373 CCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCGCCCAGCCAAACCAATC CCCACCTCGGCCTCCCAAAGTGCTGGGATTACCGGCATGAGCCACCGCGCCCAGCCAAACCAATC T G R3HDM2 Ensembl:ENSG00000179912 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1189874546 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93739,RMVar_hsa_circ_157649 34146 RMVar_ID_34146 Human_SNP_ID_502667464 A-to-I Human chr12 - 57429129 57429129 57429129 TCTGGCCTCAGACTCCCAAAAGCACTGGGATTACAGGCGTGAGCCATTGCTCTTGGCAGAGCTTC TCTGGCCTCAGACTCCCAAAAGCACTGGGATTGCAGGCGTGAGCCATTGCTCTTGGCAGAGCTTC T C R3HDM2 Ensembl:ENSG00000179912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978428258 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93739,RMVar_hsa_circ_157649 34147 RMVar_ID_34147 Human_SNP_ID_502667473 A-to-I Human chr12 - 57429169 57429169 57429169 TTGCCCAGGCTGGTTTTGAACTCCTGGCCTCAAGTGATCCTCTGGCCTCAGACTCCCAAAAGCAC TTGCCCAGGCTGGTTTTGAACTCCTGGCCTCAGGTGATCCTCTGGCCTCAGACTCCCAAAAGCAC T C R3HDM2 Ensembl:ENSG00000179912 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1421910776 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2345846 RMVar_hsa_circ_93739,RMVar_hsa_circ_157649 34148 RMVar_ID_34148 Human_SNP_ID_502667599 A-to-I Human chr12 - 57429655 57429655 57429655 AGAATGGAGTGTAGTGGTTCCTTTTCGGCTCAATGCAACCTCTGCCTCCTGGCCTCAAGCCGTCC AGAATGGAGTGTAGTGGTTCCTTTTCGGCTCAGTGCAACCTCTGCCTCCTGGCCTCAAGCCGTCC T C R3HDM2 Ensembl:ENSG00000179912 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs776246665 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11994791,Human_RBP_ID_23306041 Human_miRNA_ID_2273059,Human_miRNA_ID_2445599,Human_miRNA_ID_2446985,Human_miRNA_ID_2475801,Human_miRNA_ID_2961585 RMVar_hsa_circ_93739,RMVar_hsa_circ_157649 34149 RMVar_ID_34149 Human_SNP_ID_502678637 A-to-I Human chr12 + 57470841 57470841 57470841 CCAGCATCACTGAGAATGCTGCCATGGATGCTAGAGGGCTACAGGAAGAGCCAGAAGTTGGGACC CCAGCATCACTGAGAATGCTGCCATGGATGCTGGAGGGCTACAGGAAGAGCCAGAAGTTGGGACC A G GLI1 Ensembl:ENSG00000111087 Protein coding CDS GSE56152 embryonic stem cells,wild type - 25708366 RNA-Seq:(High) rs11553626 Functional Loss SNV dbSNP153 33..33 33 - - - 34150 RMVar_ID_34150 Human_SNP_ID_502682923 A-to-I Human chr12 + 57484738 57484738 57484738 GCGATCCCGGCTCACTGCAACCTCTGCCTCCCAAGTTCAAGCAATTCTCCTGCCTCAGCCTCCCA GCGATCCCGGCTCACTGCAACCTCTGCCTCCCGAGTTCAAGCAATTCTCCTGCCTCAGCCTCCCA A G MARS1 Ensembl:ENSG00000166986 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1467939982 Functional Loss SNV dbSNP153 33..33 33 - - - 34151 RMVar_ID_34151 Human_SNP_ID_502682924 A-to-I Human chr12 + 57484738 57484738 57484738 GCGATCCCGGCTCACTGCAACCTCTGCCTCCCAAGTTCAAGCAATTCTCCTGCCTCAGCCTCCCA GCGATCCCGGCTCACTGCAACCTCTGCCTCCCTAGTTCAAGCAATTCTCCTGCCTCAGCCTCCCA A T MARS1 Ensembl:ENSG00000166986 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1467939982 Functional Loss SNV dbSNP153 33..33 33 - - - 34152 RMVar_ID_34152 Human_SNP_ID_502687668 A-to-I Human chr12 + 57496066 57496066 57496066 ATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACTATGTTGGCTAGGCTGGTCTTGAACTGACCT ATTTTTTGTATTTTTAGTAGAGACGGGGTTTCGCTATGTTGGCTAGGCTGGTCTTGAACTGACCT A G MARS1 Ensembl:ENSG00000166986 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1270276678 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11995092 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 34153 RMVar_ID_34153 Human_SNP_ID_502687681 A-to-I Human chr12 + 57496107 57496107 57496107 GCTAGGCTGGTCTTGAACTGACCTCATGATCCACTTGTCTCGGCCTCCCAAAGTGCTGGGATTAC GCTAGGCTGGTCTTGAACTGACCTCATGATCCGCTTGTCTCGGCCTCCCAAAGTGCTGGGATTAC A G MARS1 Ensembl:ENSG00000166986 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1397812632 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11995093,Human_RBP_ID_24987944 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 34154 RMVar_ID_34154 Human_SNP_ID_502687827 A-to-I Human chr12 + 57496597 57496597 57496597 GCCCAGGAGTTCGAGACCAGTCCTGTCAACATAGACTGCATCTCTACAAAAAAAATTTAAAAATT GCCCAGGAGTTCGAGACCAGTCCTGTCAACATCGACTGCATCTCTACAAAAAAAATTTAAAAATT A C MARS1 Ensembl:ENSG00000166986 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1207087181 Functional Loss SNV dbSNP153 33..33 33 - - - 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 34155 RMVar_ID_34155 Human_SNP_ID_502687834 A-to-I Human chr12 + 57496626 57496626 57496626 CATAGACTGCATCTCTACAAAAAAAATTTAAAAATTATCCAGGCACGGTGATGCCTGCCTGAAGT CATAGACTGCATCTCTACAAAAAAAATTTAAAGATTATCCAGGCACGGTGATGCCTGCCTGAAGT A G MARS1 Ensembl:ENSG00000166986 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs528866561 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11995101 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 34156 RMVar_ID_34156 Human_SNP_ID_502691328 A-to-I Human chr12 + 57508814 57508814 57508814 AAACTTCTGACCTCAAATGATTCACCCGCCTTAGCCTCCCAAAGTGCTGGGATTACAGGTGTAAG AAACTTCTGACCTCAAATGATTCACCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGTGTAAG A G MARS1 Ensembl:ENSG00000166986 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1365057209 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112516,RMVar_hsa_circ_157661,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 34157 RMVar_ID_34157 Human_SNP_ID_502701510 A-to-I Human chr12 - 57543201 57543201 57543201 GAGACTGTAGGCGCCCACCACCACACCCGGCTAATTTTCTTGTATTTTTAGTAGAGACGGGGTTT GAGACTGTAGGCGCCCACCACCACACCCGGCTGATTTTCTTGTATTTTTAGTAGAGACGGGGTTT T C DCTN2 Ensembl:ENSG00000175203 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1344696652 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84786,RMVar_hsa_circ_100953,RMVar_hsa_circ_157682,RMVar_hsa_circ_157683,RMVar_hsa_circ_83739,RMVar_hsa_circ_157701 34158 RMVar_ID_34158 Human_SNP_ID_502701514 A-to-I Human chr12 - 57543209 57543209 57543209 GAGTAGCTGAGACTGTAGGCGCCCACCACCACACCCGGCTAATTTTCTTGTATTTTTAGTAGAGA GAGTAGCTGAGACTGTAGGCGCCCACCACCACGCCCGGCTAATTTTCTTGTATTTTTAGTAGAGA T C DCTN2 Ensembl:ENSG00000175203 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs576545275 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84786,RMVar_hsa_circ_100953,RMVar_hsa_circ_157682,RMVar_hsa_circ_157683,RMVar_hsa_circ_83739,RMVar_hsa_circ_157701 34159 RMVar_ID_34159 Human_SNP_ID_502701890 A-to-I Human chr12 - 57544579 57544579 57544579 AGACCCCGTCTCTACTAAAAAATATAAAAATTAGCAAGGCGTGGTGGCGAGCGCTTATAGTCCCA AGACCCCGTCTCTACTAAAAAATATAAAAATTGGCAAGGCGTGGTGGCGAGCGCTTATAGTCCCA T C DCTN2 Ensembl:ENSG00000175203 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1196811664 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84786,RMVar_hsa_circ_100953,RMVar_hsa_circ_157682,RMVar_hsa_circ_157683,RMVar_hsa_circ_83739,RMVar_hsa_circ_157701 34160 RMVar_ID_34160 Human_SNP_ID_502709541 A-to-I Human chr12 - 57576342 57576342 57576342 TGAGCTCATCAATGGTCTTCTGCTTCTCGTTGATCTCGTCCCGGAGCCGGGCCAGCTGCCGGTGA TGAGCTCATCAATGGTCTTCTGCTTCTCGTTGCTCTCGTCCCGGAGCCGGGCCAGCTGCCGGTGA T G RF00017-1166 RNACentral:URS00009832A9 SRP RNA intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs879254299 Functional Loss SNV dbSNP153 33..33 33 - - - 34161 RMVar_ID_34161 Human_SNP_ID_502747670 A-to-I Human chr12 + 57718168 57718168 57718168 ACCCACCCAGGGGAAGCCAAATATAGGCCAAGAGCAGCCTGTGGATGATGCTGCAGAAGTCCCTC ACCCACCCAGGGGAAGCCAAATATAGGCCAAGGGCAGCCTGTGGATGATGCTGCAGAAGTCCCTC A G OS9 Ensembl:ENSG00000135506 Protein coding CDS GSE56152 embryonic stem cells,wild type - 25708366 RNA-Seq:(High) rs752908758 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_753697,Human_RBP_ID_4235173,Human_RBP_ID_22437281,Human_RBP_ID_22756873,Human_RBP_ID_26321677 Human_Splice_Rec_1389866,Human_Splice_Rec_1389900,Human_Splice_Rec_1389946,Human_Splice_Rec_1389972,Human_Splice_Rec_1389990,Human_Splice_Rec_1390012,Human_Splice_Rec_1390036,Human_Splice_Rec_1390058,Human_Splice_Rec_1390096,Human_Splice_Rec_1390126,Human_Splice_Rec_1390140,Human_Splice_Rec_1390152 Human_miRNA_ID_40821,Human_miRNA_ID_69543,Human_miRNA_ID_1937669,Human_miRNA_ID_1948769 RMVar_hsa_circ_19152,RMVar_hsa_circ_368245,RMVar_hsa_circ_101715,RMVar_hsa_circ_157730,RMVar_hsa_circ_157733 34162 RMVar_ID_34162 Human_SNP_ID_502748771 A-to-I Human chr12 + 57722167 57722163 57722167 TTTTGTTTGTTTTGTTTCGAGACAAGAGTCTCACTCTGTTGCCCAGGCTGGAGTGCAGTGGCCTG TTTTGTTTGTTTTGTTTCGAGACAAGAGT____CTCTGTTGCCCAGGCTGGAGTGCAGTGGCCTG TCTCA T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335929012 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_8380783 34163 RMVar_ID_34163 Human_SNP_ID_502765109 A-to-I Human chr12 + 57778989 57778989 57778989 TCAAGCGATTCTCCTGCCTCAGCCTCCCTAGTAGCTGGCATTACAGGCGCCCGCCACCACACCCA TCAAGCGATTCTCCTGCCTCAGCCTCCCTAGTTGCTGGCATTACAGGCGCCCGCCACCACACCCA A T EEF1AKMT3,AC025165.3 Ensembl:ENSG00000123427,Ensembl:ENSG00000257921 Protein coding,Protein coding intron,intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1201960428 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109396,RMVar_hsa_circ_157755 34164 RMVar_ID_34164 Human_SNP_ID_502802627 A-to-I Human chr12 - 57931884 57931884 57931884 GGGTTAATCCATGTTGGTCAGGCTGGTCTCGAACTCCCAACCTCAGGTGAACCACCCACCTCAGC GGGTTAATCCATGTTGGTCAGGCTGGTCTCGAGCTCCCAACCTCAGGTGAACCACCCACCTCAGC T C GIHCG Ensembl:ENSG00000257698 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924374956 Functional Loss SNV dbSNP153 33..33 33 - - - 34165 RMVar_ID_34165 Human_SNP_ID_503246336 A-to-I Human chr12 + 59783751 59783751 59783751 TCGGCTTACTACAACCTCTGCCTCCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAAC TCGGCTTACTACAACCTCTGCCTCCCAGGTTCCAGCAATTCTCCTGCCTCAGCCTCCCGAGTAAC A C SLC16A7 Ensembl:ENSG00000118596 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line - 29129909,31158229,32596459 RNA-Seq:(High) rs969299269 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_157782 34166 RMVar_ID_34166 Human_SNP_ID_85627898 A-to-I Human chr2 + 105093569 105093556 105093570 AAAGACTGCAAAAGCAGAAGCAATTGTTTATAAACATGGAAGTGGAAGAATAAAAGTAAATGGAA AAAGACTGCAAAAGCAGAAG______________CATGGAAGTGGAAGAATAAAAGTAAATGGAA GCAATTGTTTATAAA G MRPS9 Ensembl:ENSG00000135972 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs746817782 Functional Loss DEL dbSNP153 21..34 33 - - - Human_RBP_ID_61186,Human_RBP_ID_23816425,Human_RBP_ID_26656070 Human_Splice_Rec_283838,Human_Splice_Rec_283839,Human_Splice_Rec_283850,Human_Splice_Rec_283851,Human_Splice_Rec_283854,Human_Splice_Rec_283855 RMVar_hsa_circ_11533,RMVar_hsa_circ_324772,RMVar_hsa_circ_54860,RMVar_hsa_circ_22926,RMVar_hsa_circ_67598,RMVar_hsa_circ_362018,RMVar_hsa_circ_65743 34167 RMVar_ID_34167 Human_SNP_ID_85694577 A-to-I Human chr2 + 105358884 105358884 105358884 GTTCATGCGACGAACTTGGGGCTCTCCTTTTCAGGATTTTCTTCCTCACTTTCCAGAGGCTGTTT GTTCATGCGACGAACTTGGGGCTCTCCTTTTCGGGATTTTCTTCCTCACTTTCCAGAGGCTGTTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006949496 Functional Loss SNV dbSNP153 33..33 33 - - - 34168 RMVar_ID_34168 Human_SNP_ID_85694918 A-to-I Human chr2 - 105360391 105360391 105360391 GATGGCACCACTGAACTCCAGCCTGGAAGACAAAGAGACTCCGTCTCAAAAAAAAAAAGCCTTCA GATGGCACCACTGAACTCCAGCCTGGAAGACAGAGAGACTCCGTCTCAAAAAAAAAAAGCCTTCA T C FHL2 Ensembl:ENSG00000115641 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1180606447 Functional Loss SNV dbSNP153 33..33 33 - - - 34169 RMVar_ID_34169 Human_SNP_ID_85695072 A-to-I Human chr2 - 105361083 105361083 105361083 GTTCAGTCCCAGGGAAAGAGAAAACTCGCCCTAGGCCCTAGGTGGGAAGATGGTTTGAAATTTTT GTTCAGTCCCAGGGAAAGAGAAAACTCGCCCTCGGCCCTAGGTGGGAAGATGGTTTGAAATTTTT T G FHL2 Ensembl:ENSG00000115641 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1192678906 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_57637,Human_RBP_ID_531463,Human_RBP_ID_23212076,Human_RBP_ID_24422347,Human_RBP_ID_24485676 Human_miRNA_ID_193971,Human_miRNA_ID_2008419 RMVar_hsa_circ_121656,RMVar_hsa_circ_202306,RMVar_hsa_circ_77584,RMVar_hsa_circ_202305 34170 RMVar_ID_34170 Human_SNP_ID_85697830 A-to-I Human chr2 - 105372380 105372380 105372380 TCTACTAAAAATACAAAAAATTAGCCGGGCATAGTGGCGGGCGTCTGTAGTCCCAGCTACTCGGG TCTACTAAAAATACAAAAAATTAGCCGGGCATGGTGGCGGGCGTCTGTAGTCCCAGCTACTCGGG T C FHL2 Ensembl:ENSG00000115641 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1383899798 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_371869,RMVar_hsa_circ_202308,RMVar_hsa_circ_284600,RMVar_hsa_circ_202307,RMVar_hsa_circ_307296,RMVar_hsa_circ_202309,RMVar_hsa_circ_86098 34171 RMVar_ID_34171 Human_SNP_ID_85702122 A-to-I Human chr2 - 105390179 105390179 105390179 TCGCCCAGGCTGGAGTGCAGTGGCACGATCTCAGCTCACTGCAAGCTCTACCTCTTGGTTCACGC TCGCCCAGGCTGGAGTGCAGTGGCACGATCTCGGCTCACTGCAAGCTCTACCTCTTGGTTCACGC T C FHL2 Ensembl:ENSG00000115641 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs578040007 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_284026,Human_Splice_Rec_284027,Human_Splice_Rec_284090 RMVar_hsa_circ_202310,RMVar_hsa_circ_121656,RMVar_hsa_circ_202306,RMVar_hsa_circ_86098 34172 RMVar_ID_34172 Human_SNP_ID_85802350 A-to-I Human chr2 + 105779225 105779225 105779225 GCTACTCTGGAGGCTGAGGCATGAGAATCGCTAGAAACTGGGAGACAGAGGTTGCAGTGAGCCGA GCTACTCTGGAGGCTGAGGCATGAGAATCGCTGGAAACTGGGAGACAGAGGTTGCAGTGAGCCGA A G NCK2 Ensembl:ENSG00000071051 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1455580607 Functional Loss SNV dbSNP153 33..33 33 - - - 34173 RMVar_ID_34173 Human_SNP_ID_86482329 A-to-I Human chr2 + 108453623 108453623 108453623 CCTGGCCAGCATGGTGAAACCCTGTCTGTACTAAAAATACAACATTTAGCTGGGCGTGATTGCCC CCTGGCCAGCATGGTGAAACCCTGTCTGTACTGAAAATACAACATTTAGCTGGGCGTGATTGCCC A G GCC2 Ensembl:ENSG00000135968 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs766715241 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_202359,RMVar_hsa_circ_105892,RMVar_hsa_circ_104986,RMVar_hsa_circ_202361,RMVar_hsa_circ_10872,RMVar_hsa_circ_63227,RMVar_hsa_circ_58349,RMVar_hsa_circ_272696,RMVar_hsa_circ_280307,RMVar_hsa_circ_93826,RMVar_hsa_circ_104987,RMVar_hsa_circ_202365,RMVar_hsa_circ_326070,RMVar_hsa_circ_202364,RMVar_hsa_circ_324561,RMVar_hsa_circ_40589,RMVar_hsa_circ_65028,RMVar_hsa_circ_39937,RMVar_hsa_circ_202367,RMVar_hsa_circ_202368,RMVar_hsa_circ_202369 34174 RMVar_ID_34174 Human_SNP_ID_86488841 A-to-I Human chr2 + 108476260 108476260 108476260 TTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGCTGGCCAGGCTGGTCTTGAACTCCTGACCT TTTTGTATTTTTAGTAGAGACGGGGTTTCACCCTGCTGGCCAGGCTGGTCTTGAACTCCTGACCT A C GCC2 Ensembl:ENSG00000135968 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs995390051 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_202359,RMVar_hsa_circ_105892,RMVar_hsa_circ_104986,RMVar_hsa_circ_202361,RMVar_hsa_circ_10872,RMVar_hsa_circ_63227,RMVar_hsa_circ_280307,RMVar_hsa_circ_93826,RMVar_hsa_circ_104987,RMVar_hsa_circ_202364,RMVar_hsa_circ_40589,RMVar_hsa_circ_39937,RMVar_hsa_circ_63412,RMVar_hsa_circ_202371,RMVar_hsa_circ_202369,RMVar_hsa_circ_87936,RMVar_hsa_circ_297431,RMVar_hsa_circ_202372,RMVar_hsa_circ_27481,RMVar_hsa_circ_202373,RMVar_hsa_circ_373714,RMVar_hsa_circ_359976,RMVar_hsa_circ_369081,RMVar_hsa_circ_118476,RMVar_hsa_circ_357140,RMVar_hsa_circ_351366,RMVar_hsa_circ_202375,RMVar_hsa_circ_16096,RMVar_hsa_circ_47726,RMVar_hsa_circ_202376 34175 RMVar_ID_34175 Human_SNP_ID_86495700 A-to-I Human chr2 + 108501095 108501095 108501095 ATGGCTCACTGCAACCTCCGCCTCCCAGATTCAAGCGATTCTCCTGCCTCAGCCTCCCCAGCAGC ATGGCTCACTGCAACCTCCGCCTCCCAGATTCGAGCGATTCTCCTGCCTCAGCCTCCCCAGCAGC A G GCC2 Ensembl:ENSG00000135968 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1378948563 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_202359,RMVar_hsa_circ_105892,RMVar_hsa_circ_104986,RMVar_hsa_circ_202361 34176 RMVar_ID_34176 Human_SNP_ID_86496131 A-to-I Human chr2 - 108502757 108502753 108502758 CACCACGCCCGGCTAATTTTTGTATTCTGAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGG CACCACGCCCGGCTAATTTTTGTATTCTGAG_____ACGGGGTTTCACCATGTTGGCCAGGCTGG TCTCTA T GCC2-AS1,GCC2-AS1:2,GCC2-AS1:3,GCC2-AS1:4,GCC2-AS1:5 RNACentral:URS00009AD569,RNACentral:URS0000D5D967,RNACentral:URS0000D58C9E,RNACentral:URS0000D5954B,RNACentral:URS00009AFD4A lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,exon,exon,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1376837462 Functional Loss DEL dbSNP153 32..36 33 - - - 34177 RMVar_ID_34177 Human_SNP_ID_86496132 A-to-I Human chr2 - 108502757 108502757 108502757 CACCACGCCCGGCTAATTTTTGTATTCTGAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGG CACCACGCCCGGCTAATTTTTGTATTCTGAGTCGAGACGGGGTTTCACCATGTTGGCCAGGCTGG T G GCC2-AS1,GCC2-AS1:2,GCC2-AS1:3,GCC2-AS1:4,GCC2-AS1:5 RNACentral:URS00009AD569,RNACentral:URS0000D5D967,RNACentral:URS0000D58C9E,RNACentral:URS0000D5954B,RNACentral:URS00009AFD4A lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,exon,exon,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1275720956 Functional Loss SNV dbSNP153 33..33 33 - - - 34178 RMVar_ID_34178 Human_SNP_ID_86509920 A-to-I Human chr2 + 108552039 108552039 108552039 TTCAATCTGAACGTCCAGGATTTGTGAGAAGTACAGAGGTCTCTAATGTGTGTATATGTGTGTGT TTCAATCTGAACGTCCAGGATTTGTGAGAAGTGCAGAGGTCTCTAATGTGTGTATATGTGTGTGT A G LIMS1 Ensembl:ENSG00000169756 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1162089160 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569835 RMVar_hsa_circ_202359,RMVar_hsa_circ_105892,RMVar_hsa_circ_104986,RMVar_hsa_circ_202361 34179 RMVar_ID_34179 Human_SNP_ID_86512456 A-to-I Human chr2 + 108561822 108561822 108561822 GGAGTGCAGTGGCGTGATCTTGGCTCAACTGCAACCTCTGCCTCCCGGGTTCAAGCAACTCTCAT GGAGTGCAGTGGCGTGATCTTGGCTCAACTGCCACCTCTGCCTCCCGGGTTCAAGCAACTCTCAT A C LIMS1 Ensembl:ENSG00000169756 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs955788197 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13571732 RMVar_hsa_circ_202359,RMVar_hsa_circ_105892,RMVar_hsa_circ_104986,RMVar_hsa_circ_202361 34180 RMVar_ID_34180 Human_SNP_ID_86517784 A-to-I Human chr2 + 108583764 108583764 108583764 TCGCTCAGGCTGGAGTGCAGTGGTGTGATCTCAGCTTACTGCAACCTCTGCCTCCTGGGTTCAAG TCGCTCAGGCTGGAGTGCAGTGGTGTGATCTCGGCTTACTGCAACCTCTGCCTCCTGGGTTCAAG A G LIMS1 Ensembl:ENSG00000169756 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971090815 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_202359,RMVar_hsa_circ_105892,RMVar_hsa_circ_104986,RMVar_hsa_circ_202361 34181 RMVar_ID_34181 Human_SNP_ID_86518095 A-to-I Human chr2 + 108585040 108585040 108585040 GAGCGTGGTGGCACGTGCCTGTTGACCCAGCTACTTGGGAGGCTGAGGCAGGAAAATGACTTGAA GAGCGTGGTGGCACGTGCCTGTTGACCCAGCTGCTTGGGAGGCTGAGGCAGGAAAATGACTTGAA A G LIMS1 Ensembl:ENSG00000169756 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1558797249 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_202359,RMVar_hsa_circ_105892,RMVar_hsa_circ_104986,RMVar_hsa_circ_202361 34182 RMVar_ID_34182 Human_SNP_ID_86540003 A-to-I Human chr2 + 108673516 108673516 108673516 TCAAGCAGTCCTCCCACTTCAGCCTCCAGAGTAGCTGAGACCACAGGCACACACCACCCTTCCTG TCAAGCAGTCCTCCCACTTCAGCCTCCAGAGTGGCTGAGACCACAGGCACACACCACCCTTCCTG A G LIMS1 Ensembl:ENSG00000169756 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1412094623 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_202359,RMVar_hsa_circ_105892,RMVar_hsa_circ_104986,RMVar_hsa_circ_202361,RMVar_hsa_circ_105814,RMVar_hsa_circ_95513,RMVar_hsa_circ_22769,RMVar_hsa_circ_52491,RMVar_hsa_circ_202388,RMVar_hsa_circ_104339,RMVar_hsa_circ_126765,RMVar_hsa_circ_202391,RMVar_hsa_circ_16971,RMVar_hsa_circ_124353,RMVar_hsa_circ_202394,RMVar_hsa_circ_202395,RMVar_hsa_circ_202393,RMVar_hsa_circ_126189,RMVar_hsa_circ_202396 34183 RMVar_ID_34183 Human_SNP_ID_86545379 A-to-I Human chr2 - 108694809 108694809 108694809 TTGCTATATGGACATATGTAGCAACACAAATCAGAATAGAATGGAACCTGTGCCCTGGTGGCAGA TTGCTATATGGACATATGTAGCAACACAAATCGGAATAGAATGGAACCTGTGCCCTGGTGGCAGA T C AC010095.1 Ensembl:ENSG00000233648 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs955731382 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26999193,Human_RBP_ID_27281436 34184 RMVar_ID_34184 Human_SNP_ID_86545380 A-to-I Human chr2 - 108694812 108694812 108694812 GTATTGCTATATGGACATATGTAGCAACACAAATCAGAATAGAATGGAACCTGTGCCCTGGTGGC GTATTGCTATATGGACATATGTAGCAACACAAGTCAGAATAGAATGGAACCTGTGCCCTGGTGGC T C AC010095.1 Ensembl:ENSG00000233648 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs989752822 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26999193,Human_RBP_ID_27281436 34185 RMVar_ID_34185 Human_SNP_ID_86545398 A-to-I Human chr2 - 108694877 108694877 108694877 AGAAAAGTACACCTGATTTTCATGACAATACGATAATGCTGTATTAGCTAGTGGAGCCACTTTCT AGAAAAGTACACCTGATTTTCATGACAATACGGTAATGCTGTATTAGCTAGTGGAGCCACTTTCT T C AC010095.1 Ensembl:ENSG00000233648 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs990516738 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1866449,Human_miRNA_ID_1877554,Human_miRNA_ID_1901808,Human_miRNA_ID_2531707,Human_miRNA_ID_2666810,Human_miRNA_ID_2982798 34186 RMVar_ID_34186 Human_SNP_ID_86552277 A-to-I Human chr2 + 108720969 108720969 108720969 TACCCGGGAGGCTGAGGCAGGAGAGTCGCTTGAACCCGGGAGGCGGAGGTTCCAGTGAGCCGAGA TACCCGGGAGGCTGAGGCAGGAGAGTCGCTTGGACCCGGGAGGCGGAGGTTCCAGTGAGCCGAGA A G RANBP2 Ensembl:ENSG00000153201 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913194236 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_202359,RMVar_hsa_circ_105892,RMVar_hsa_circ_104986,RMVar_hsa_circ_202361,RMVar_hsa_circ_87241,RMVar_hsa_circ_202399 34187 RMVar_ID_34187 Human_SNP_ID_86560930 A-to-I Human chr2 + 108750066 108750066 108750066 TACTCAGGAGGCTGAGGCAGGGGAATCGCTTCAACCCGGGAGGCGGAGGTTGCAGTGAGCCAAGA TACTCAGGAGGCTGAGGCAGGGGAATCGCTTCGACCCGGGAGGCGGAGGTTGCAGTGAGCCAAGA A G RANBP2 Ensembl:ENSG00000153201 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1177453731 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_202359,RMVar_hsa_circ_105892,RMVar_hsa_circ_104986,RMVar_hsa_circ_202361,RMVar_hsa_circ_31226,RMVar_hsa_circ_104797,RMVar_hsa_circ_337676,RMVar_hsa_circ_34376,RMVar_hsa_circ_202400,RMVar_hsa_circ_75726,RMVar_hsa_circ_202404,RMVar_hsa_circ_49242,RMVar_hsa_circ_42180,RMVar_hsa_circ_202402,RMVar_hsa_circ_326272,RMVar_hsa_circ_345514,RMVar_hsa_circ_10628,RMVar_hsa_circ_83350,RMVar_hsa_circ_344567 34188 RMVar_ID_34188 Human_SNP_ID_86572862 A-to-I Human chr2 + 108790996 108790995 108790997 GTTGTCCAGGCTGATCTTGAACTCCTGGGCTCAAGAGATACTCCCACTTCGGCCTCCCAAAGTGC GTTGTCCAGGCTGATCTTGAACTCCTGGGCTC__GAGATACTCCCACTTCGGCCTCCCAAAGTGC CAA C CCDC138 Ensembl:ENSG00000163006 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256523003 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_13573820 RMVar_hsa_circ_73427,RMVar_hsa_circ_366399,RMVar_hsa_circ_332383,RMVar_hsa_circ_202419,RMVar_hsa_circ_202423,RMVar_hsa_circ_280280,RMVar_hsa_circ_312788,RMVar_hsa_circ_322442,RMVar_hsa_circ_346789,RMVar_hsa_circ_61040,RMVar_hsa_circ_333588,RMVar_hsa_circ_321453,RMVar_hsa_circ_285573,RMVar_hsa_circ_307438,RMVar_hsa_circ_281888,RMVar_hsa_circ_202425,RMVar_hsa_circ_202426,RMVar_hsa_circ_202424,RMVar_hsa_circ_202421,RMVar_hsa_circ_202422,RMVar_hsa_circ_202420,RMVar_hsa_circ_202418 34189 RMVar_ID_34189 Human_SNP_ID_86579862 A-to-I Human chr2 + 108816899 108816899 108816899 AAAAAATTTTTGTAGAGATCAGACCTGGCTTCATTGCACAGAATGATCTTGAACTCTTAGCTTCA AAAAAATTTTTGTAGAGATCAGACCTGGCTTCGTTGCACAGAATGATCTTGAACTCTTAGCTTCA A G CCDC138 Ensembl:ENSG00000163006 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1330331476 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13574158 RMVar_hsa_circ_1832,RMVar_hsa_circ_202419,RMVar_hsa_circ_322442,RMVar_hsa_circ_61040,RMVar_hsa_circ_321453,RMVar_hsa_circ_285573,RMVar_hsa_circ_307438,RMVar_hsa_circ_202421,RMVar_hsa_circ_202420,RMVar_hsa_circ_202428,RMVar_hsa_circ_50855,RMVar_hsa_circ_310556,RMVar_hsa_circ_202418,RMVar_hsa_circ_334321,RMVar_hsa_circ_330969,RMVar_hsa_circ_202429,RMVar_hsa_circ_312106,RMVar_hsa_circ_202427,RMVar_hsa_circ_340700,RMVar_hsa_circ_60824,RMVar_hsa_circ_7617,RMVar_hsa_circ_202435,RMVar_hsa_circ_354291,RMVar_hsa_circ_56541,RMVar_hsa_circ_367176,RMVar_hsa_circ_47418,RMVar_hsa_circ_338589,RMVar_hsa_circ_348107,RMVar_hsa_circ_57295 34190 RMVar_ID_34190 Human_SNP_ID_86580157 A-to-I Human chr2 + 108818152 108818152 108818152 ACATGGTGACACCCCATCTCTACAAAAAATACAAAAGTTAGCCAGGCCTGGTGGCACGCGCCTAT ACATGGTGACACCCCATCTCTACAAAAAATACGAAAGTTAGCCAGGCCTGGTGGCACGCGCCTAT A G CCDC138 Ensembl:ENSG00000163006 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs959014586 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1832,RMVar_hsa_circ_202419,RMVar_hsa_circ_322442,RMVar_hsa_circ_61040,RMVar_hsa_circ_321453,RMVar_hsa_circ_285573,RMVar_hsa_circ_307438,RMVar_hsa_circ_202421,RMVar_hsa_circ_202420,RMVar_hsa_circ_202428,RMVar_hsa_circ_50855,RMVar_hsa_circ_310556,RMVar_hsa_circ_202418,RMVar_hsa_circ_334321,RMVar_hsa_circ_330969,RMVar_hsa_circ_202429,RMVar_hsa_circ_312106,RMVar_hsa_circ_202427,RMVar_hsa_circ_340700,RMVar_hsa_circ_60824,RMVar_hsa_circ_7617,RMVar_hsa_circ_202435,RMVar_hsa_circ_354291,RMVar_hsa_circ_56541,RMVar_hsa_circ_367176,RMVar_hsa_circ_47418,RMVar_hsa_circ_338589,RMVar_hsa_circ_348107,RMVar_hsa_circ_57295 34191 RMVar_ID_34191 Human_SNP_ID_86580158 A-to-I Human chr2 + 108818153 108818153 108818153 CATGGTGACACCCCATCTCTACAAAAAATACAAAAGTTAGCCAGGCCTGGTGGCACGCGCCTATA CATGGTGACACCCCATCTCTACAAAAAATACAGAAGTTAGCCAGGCCTGGTGGCACGCGCCTATA A G CCDC138 Ensembl:ENSG00000163006 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1369315201 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1832,RMVar_hsa_circ_202419,RMVar_hsa_circ_322442,RMVar_hsa_circ_61040,RMVar_hsa_circ_321453,RMVar_hsa_circ_285573,RMVar_hsa_circ_307438,RMVar_hsa_circ_202421,RMVar_hsa_circ_202420,RMVar_hsa_circ_202428,RMVar_hsa_circ_50855,RMVar_hsa_circ_310556,RMVar_hsa_circ_202418,RMVar_hsa_circ_334321,RMVar_hsa_circ_330969,RMVar_hsa_circ_202429,RMVar_hsa_circ_312106,RMVar_hsa_circ_202427,RMVar_hsa_circ_340700,RMVar_hsa_circ_60824,RMVar_hsa_circ_7617,RMVar_hsa_circ_202435,RMVar_hsa_circ_354291,RMVar_hsa_circ_56541,RMVar_hsa_circ_367176,RMVar_hsa_circ_47418,RMVar_hsa_circ_338589,RMVar_hsa_circ_348107,RMVar_hsa_circ_57295 34192 RMVar_ID_34192 Human_SNP_ID_86580176 A-to-I Human chr2 + 108818215 108818215 108818215 ATAACCCCAGTTCCCTGGGAGGCTGAGGTGGTAGGATCACCTGAACCTGGGGGGGTCGAGGCTGC ATAACCCCAGTTCCCTGGGAGGCTGAGGTGGTGGGATCACCTGAACCTGGGGGGGTCGAGGCTGC A G CCDC138 Ensembl:ENSG00000163006 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs931247438 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1832,RMVar_hsa_circ_202419,RMVar_hsa_circ_322442,RMVar_hsa_circ_61040,RMVar_hsa_circ_321453,RMVar_hsa_circ_285573,RMVar_hsa_circ_307438,RMVar_hsa_circ_202421,RMVar_hsa_circ_202420,RMVar_hsa_circ_202428,RMVar_hsa_circ_50855,RMVar_hsa_circ_310556,RMVar_hsa_circ_202418,RMVar_hsa_circ_334321,RMVar_hsa_circ_330969,RMVar_hsa_circ_202429,RMVar_hsa_circ_312106,RMVar_hsa_circ_202427,RMVar_hsa_circ_340700,RMVar_hsa_circ_60824,RMVar_hsa_circ_7617,RMVar_hsa_circ_202435,RMVar_hsa_circ_354291,RMVar_hsa_circ_56541,RMVar_hsa_circ_367176,RMVar_hsa_circ_47418,RMVar_hsa_circ_338589,RMVar_hsa_circ_348107,RMVar_hsa_circ_57295 34193 RMVar_ID_34193 Human_SNP_ID_86580205 A-to-I Human chr2 + 108818289 108818289 108818289 TGATTGTACCACTGTACTCCAGCCTGGGCAACAGAGTGAGACCCTGTCTGAAGAAAAATAATGGA TGATTGTACCACTGTACTCCAGCCTGGGCAACGGAGTGAGACCCTGTCTGAAGAAAAATAATGGA A G CCDC138 Ensembl:ENSG00000163006 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904665448 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13574212,Human_RBP_ID_18744072 RMVar_hsa_circ_1832,RMVar_hsa_circ_202419,RMVar_hsa_circ_322442,RMVar_hsa_circ_61040,RMVar_hsa_circ_321453,RMVar_hsa_circ_285573,RMVar_hsa_circ_307438,RMVar_hsa_circ_202421,RMVar_hsa_circ_202420,RMVar_hsa_circ_202428,RMVar_hsa_circ_50855,RMVar_hsa_circ_310556,RMVar_hsa_circ_202418,RMVar_hsa_circ_334321,RMVar_hsa_circ_330969,RMVar_hsa_circ_202429,RMVar_hsa_circ_312106,RMVar_hsa_circ_202427,RMVar_hsa_circ_340700,RMVar_hsa_circ_60824,RMVar_hsa_circ_7617,RMVar_hsa_circ_202435,RMVar_hsa_circ_354291,RMVar_hsa_circ_56541,RMVar_hsa_circ_367176,RMVar_hsa_circ_47418,RMVar_hsa_circ_338589,RMVar_hsa_circ_348107,RMVar_hsa_circ_57295 34194 RMVar_ID_34194 Human_SNP_ID_86582765 A-to-I Human chr2 + 108828520 108828520 108828520 ATACTGACATAAGACATGTAGACCAATGGGATAGAATGGAGAGCCCAATATAAGCCCTCACATAT ATACTGACATAAGACATGTAGACCAATGGGATGGAATGGAGAGCCCAATATAAGCCCTCACATAT A G CCDC138 Ensembl:ENSG00000163006 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1244418840 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13574413 RMVar_hsa_circ_1832,RMVar_hsa_circ_202419,RMVar_hsa_circ_322442,RMVar_hsa_circ_61040,RMVar_hsa_circ_321453,RMVar_hsa_circ_285573,RMVar_hsa_circ_307438,RMVar_hsa_circ_202421,RMVar_hsa_circ_202420,RMVar_hsa_circ_202428,RMVar_hsa_circ_50855,RMVar_hsa_circ_310556,RMVar_hsa_circ_202418,RMVar_hsa_circ_334321,RMVar_hsa_circ_330969,RMVar_hsa_circ_202429,RMVar_hsa_circ_312106,RMVar_hsa_circ_202427,RMVar_hsa_circ_340700,RMVar_hsa_circ_60824,RMVar_hsa_circ_7617,RMVar_hsa_circ_202435,RMVar_hsa_circ_354291,RMVar_hsa_circ_56541,RMVar_hsa_circ_367176,RMVar_hsa_circ_47418,RMVar_hsa_circ_338589,RMVar_hsa_circ_348107,RMVar_hsa_circ_57295 34195 RMVar_ID_34195 Human_SNP_ID_86583677 A-to-I Human chr2 + 108831812 108831812 108831812 TGGAGCGCAATGGCATGATCTCGGCCCACTGCAACTACTGCCTCCTGGGTTCAAGCGATTCTCCT TGGAGCGCAATGGCATGATCTCGGCCCACTGCGACTACTGCCTCCTGGGTTCAAGCGATTCTCCT A G CCDC138 Ensembl:ENSG00000163006 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs531604077 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1832,RMVar_hsa_circ_202419,RMVar_hsa_circ_322442,RMVar_hsa_circ_61040,RMVar_hsa_circ_321453,RMVar_hsa_circ_285573,RMVar_hsa_circ_307438,RMVar_hsa_circ_202421,RMVar_hsa_circ_202420,RMVar_hsa_circ_202428,RMVar_hsa_circ_50855,RMVar_hsa_circ_310556,RMVar_hsa_circ_202418,RMVar_hsa_circ_334321,RMVar_hsa_circ_330969,RMVar_hsa_circ_202429,RMVar_hsa_circ_312106,RMVar_hsa_circ_202427,RMVar_hsa_circ_340700,RMVar_hsa_circ_60824,RMVar_hsa_circ_7617,RMVar_hsa_circ_202435,RMVar_hsa_circ_354291,RMVar_hsa_circ_56541,RMVar_hsa_circ_367176,RMVar_hsa_circ_47418,RMVar_hsa_circ_338589,RMVar_hsa_circ_348107,RMVar_hsa_circ_57295 34196 RMVar_ID_34196 Human_SNP_ID_86766641 A-to-I Human chr2 - 109550166 109550166 109550166 CCTGCCTCAGCCTCCCGAGTAGCTGGGATTATAGGCATGTGCCACCATGCCCAGCTAATTTTGTA CCTGCCTCAGCCTCCCGAGTAGCTGGGATTATGGGCATGTGCCACCATGCCCAGCTAATTTTGTA T C SEPTIN10 Ensembl:ENSG00000186522 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1418768429 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4144,RMVar_hsa_circ_376335,RMVar_hsa_circ_202455 34197 RMVar_ID_34197 Human_SNP_ID_86769439 A-to-I Human chr2 - 109561890 109561890 109561890 TGCCTGCCTTGGGCTCCTGAAGTGATGGGATTACAGTGATGGATCACACCTGGCTAAGGATATGT TGCCTGCCTTGGGCTCCTGAAGTGATGGGATTGCAGTGATGGATCACACCTGGCTAAGGATATGT T C SEPTIN10 Ensembl:ENSG00000186522 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1395099026 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569840 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 34198 RMVar_ID_34198 Human_SNP_ID_86769477 A-to-I Human chr2 - 109562039 109562039 109562039 CCAGCTAATTTTTGTGTTTTTGTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTTGA CCAGCTAATTTTTGTGTTTTTGTAGTAGAGACTGGGTTTCACCATGTTGGCCAGGCTGGTCTTGA T A SEPTIN10 Ensembl:ENSG00000186522 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs567471094 Functional Loss SNV dbSNP153 33..33 33 - - - 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 34199 RMVar_ID_34199 Human_SNP_ID_86776912 A-to-I Human chr2 - 109590569 109590567 109590570 AAATTAGTCAGCTGTGGTGGCAAGCACCTATAATCCTAGCTGCTCGAGAGGCTGAGGCAGGAGAA AAATTAGTCAGCTGTGGTGGCAAGCACCTAT___CCTAGCTGCTCGAGAGGCTGAGGCAGGAGAA GATT G SEPTIN10 Ensembl:ENSG00000186522 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs377584868 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_376335,RMVar_hsa_circ_272325,RMVar_hsa_circ_202455,RMVar_hsa_circ_202457,RMVar_hsa_circ_273970,RMVar_hsa_circ_5705,RMVar_hsa_circ_90874,RMVar_hsa_circ_202465,RMVar_hsa_circ_202459,RMVar_hsa_circ_202460,RMVar_hsa_circ_333762,RMVar_hsa_circ_286736,RMVar_hsa_circ_274078,RMVar_hsa_circ_202470,RMVar_hsa_circ_202468,RMVar_hsa_circ_280646,RMVar_hsa_circ_47045 34200 RMVar_ID_34200 Human_SNP_ID_86782008 A-to-I Human chr2 - 109610227 109610227 109610227 GAAATTAGCTGGGCTTGGTGGCATGCGCCTGTAGTCCCAACTACTTGGGAGGCTGAGGCAGGAGG GAAATTAGCTGGGCTTGGTGGCATGCGCCTGTGGTCCCAACTACTTGGGAGGCTGAGGCAGGAGG T C SEPTIN10 Ensembl:ENSG00000186522 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs898325457 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90874,RMVar_hsa_circ_202459 34201 RMVar_ID_34201 Human_SNP_ID_86796444 A-to-I Human chr2 - 109665272 109665272 109665272 GATGGATTCGTGGTCCTTGGCATCAATGATGCAGTTGCTATCGGACCATTTCCACGGCACGTACA GATGGATTCGTGGTCCTTGGCATCAATGATGCGGTTGCTATCGGACCATTTCCACGGCACGTACA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1325872119 Functional Loss SNV dbSNP153 33..33 33 - - - 34202 RMVar_ID_34202 Human_SNP_ID_86892496 A-to-I Human chr2 - 110375399 110375399 110375399 GGATCTGTGATGAGATCGGGAAAGTGGGCTCAAGAGGTCTGGATCTGTGGTGAGATGGGGGAAGT GGATCTGTGATGAGATCGGGAAAGTGGGCTCAGGAGGTCTGGATCTGTGGTGAGATGGGGGAAGT T C LINC01106 Ensembl:ENSG00000175772 lincRNA exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1277278542 Functional Loss SNV dbSNP153 33..33 33 - - - 34203 RMVar_ID_34203 Human_SNP_ID_87052322 A-to-I Human chr2 - 111242316 111242315 111242317 CTATACTTATTTAACTTTTTTTTTTTTGAGACAGAGTCTCCCTCTGTCACCCAGGCTGGAATGCA CTATACTTATTTAACTTTTTTTTTTTTGAGA__GAGTCTCCCTCTGTCACCCAGGCTGGAATGCA CTG C MIR4435-2HG Ensembl:ENSG00000172965 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1489195744 Functional Loss DEL dbSNP153 32..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,RMVar_hsa_circ_46678,RMVar_hsa_circ_80963,RMVar_hsa_circ_304253,RMVar_hsa_circ_202526,RMVar_hsa_circ_347098,RMVar_hsa_circ_338418,RMVar_hsa_circ_13022 34204 RMVar_ID_34204 Human_SNP_ID_87107407 A-to-I Human chr2 - 111488756 111488756 111488756 CCAATGAAAGATATAGGCTGAAAGGGTTAGCTAGGGATTCTAGAAAAGCTCTCTAAAGGAGACTG CCAATGAAAGATATAGGCTGAAAGGGTTAGCTCGGGATTCTAGAAAAGCTCTCTAAAGGAGACTG T G MIR4435-2HG,AC017002.4 Ensembl:ENSG00000172965,Ensembl:ENSG00000285016 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1399127243 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22980927 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 34205 RMVar_ID_34205 Human_SNP_ID_87191631 A-to-I Human chr2 - 111836499 111836499 111836499 GGACTACCGGTATGCTCCATCACGCCTGGCTAATTTTTAAATTTTTTTGGTAGAGACAAGGTGTT GGACTACCGGTATGCTCCATCACGCCTGGCTAGTTTTTAAATTTTTTTGGTAGAGACAAGGTGTT T C ANAPC1 Ensembl:ENSG00000153107 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1466566881 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,RMVar_hsa_circ_12789,RMVar_hsa_circ_91140,RMVar_hsa_circ_79739,RMVar_hsa_circ_115405,RMVar_hsa_circ_202535,RMVar_hsa_circ_111696,RMVar_hsa_circ_94820,RMVar_hsa_circ_202537,RMVar_hsa_circ_202538,RMVar_hsa_circ_202536,RMVar_hsa_circ_202539,RMVar_hsa_circ_126434,RMVar_hsa_circ_202540,RMVar_hsa_circ_95960,RMVar_hsa_circ_202543,RMVar_hsa_circ_116724,RMVar_hsa_circ_110379,RMVar_hsa_circ_202544,RMVar_hsa_circ_202547,RMVar_hsa_circ_100304,RMVar_hsa_circ_127752,RMVar_hsa_circ_61521,RMVar_hsa_circ_202550,RMVar_hsa_circ_202549,RMVar_hsa_circ_121876,RMVar_hsa_circ_77817,RMVar_hsa_circ_202551,RMVar_hsa_circ_202552,RMVar_hsa_circ_112777,RMVar_hsa_circ_87443,RMVar_hsa_circ_202555,RMVar_hsa_circ_115674,RMVar_hsa_circ_88602,RMVar_hsa_circ_202556,RMVar_hsa_circ_202557,RMVar_hsa_circ_105494,RMVar_hsa_circ_202558,RMVar_hsa_circ_202559,RMVar_hsa_circ_66068,RMVar_hsa_circ_114578,RMVar_hsa_circ_357029,RMVar_hsa_circ_115293,RMVar_hsa_circ_64008,RMVar_hsa_circ_65999,RMVar_hsa_circ_51456,RMVar_hsa_circ_76015,RMVar_hsa_circ_77552,RMVar_hsa_circ_117562,RMVar_hsa_circ_202561,RMVar_hsa_circ_202562,RMVar_hsa_circ_202560,RMVar_hsa_circ_87416,RMVar_hsa_circ_125054,RMVar_hsa_circ_202564,RMVar_hsa_circ_202565,RMVar_hsa_circ_364250,RMVar_hsa_circ_202563,RMVar_hsa_circ_355552,RMVar_hsa_circ_107377,RMVar_hsa_circ_81944,RMVar_hsa_circ_81374,RMVar_hsa_circ_202566,RMVar_hsa_circ_202568,RMVar_hsa_circ_202569,RMVar_hsa_circ_202567,RMVar_hsa_circ_20693,RMVar_hsa_circ_329748,RMVar_hsa_circ_343103,RMVar_hsa_circ_359476,RMVar_hsa_circ_85860,RMVar_hsa_circ_115977,RMVar_hsa_circ_202571,RMVar_hsa_circ_202572,RMVar_hsa_circ_333681,RMVar_hsa_circ_102996,RMVar_hsa_circ_112337,RMVar_hsa_circ_202573,RMVar_hsa_circ_202575,RMVar_hsa_circ_80879,RMVar_hsa_circ_202576,RMVar_hsa_circ_202574,RMVar_hsa_circ_128114,RMVar_hsa_circ_363398,RMVar_hsa_circ_104865,RMVar_hsa_circ_110641,RMVar_hsa_circ_88865,RMVar_hsa_circ_202577,RMVar_hsa_circ_202579,RMVar_hsa_circ_202580,RMVar_hsa_circ_202581,RMVar_hsa_circ_202578 34206 RMVar_ID_34206 Human_SNP_ID_87193409 A-to-I Human chr2 - 111843917 111843917 111843917 TGGTGGCTGAGGTAGGAGAATCGCTTGAACTCAGGAGGCAGAAGTTGCAGTGTGCCAAGACCGTG TGGTGGCTGAGGTAGGAGAATCGCTTGAACTCGGGAGGCAGAAGTTGCAGTGTGCCAAGACCGTG T C ANAPC1 Ensembl:ENSG00000153107 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1312548107 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,RMVar_hsa_circ_91140,RMVar_hsa_circ_79739,RMVar_hsa_circ_115405,RMVar_hsa_circ_202535,RMVar_hsa_circ_111696,RMVar_hsa_circ_94820,RMVar_hsa_circ_202537,RMVar_hsa_circ_202538,RMVar_hsa_circ_202536,RMVar_hsa_circ_202539,RMVar_hsa_circ_126434,RMVar_hsa_circ_202540,RMVar_hsa_circ_95960,RMVar_hsa_circ_202543,RMVar_hsa_circ_116724,RMVar_hsa_circ_110379,RMVar_hsa_circ_202544,RMVar_hsa_circ_202547,RMVar_hsa_circ_100304,RMVar_hsa_circ_127752,RMVar_hsa_circ_61521,RMVar_hsa_circ_202550,RMVar_hsa_circ_202549,RMVar_hsa_circ_121876,RMVar_hsa_circ_77817,RMVar_hsa_circ_202551,RMVar_hsa_circ_202552,RMVar_hsa_circ_112777,RMVar_hsa_circ_87443,RMVar_hsa_circ_202555,RMVar_hsa_circ_115674,RMVar_hsa_circ_88602,RMVar_hsa_circ_202556,RMVar_hsa_circ_202557,RMVar_hsa_circ_105494,RMVar_hsa_circ_202558,RMVar_hsa_circ_202559,RMVar_hsa_circ_66068,RMVar_hsa_circ_114578,RMVar_hsa_circ_357029,RMVar_hsa_circ_115293,RMVar_hsa_circ_64008,RMVar_hsa_circ_65999,RMVar_hsa_circ_51456,RMVar_hsa_circ_76015,RMVar_hsa_circ_77552,RMVar_hsa_circ_117562,RMVar_hsa_circ_202561,RMVar_hsa_circ_202562,RMVar_hsa_circ_202560,RMVar_hsa_circ_87416,RMVar_hsa_circ_125054,RMVar_hsa_circ_202564,RMVar_hsa_circ_202565,RMVar_hsa_circ_202563,RMVar_hsa_circ_355552,RMVar_hsa_circ_107377,RMVar_hsa_circ_81944,RMVar_hsa_circ_81374,RMVar_hsa_circ_202566,RMVar_hsa_circ_202568,RMVar_hsa_circ_202569,RMVar_hsa_circ_202567,RMVar_hsa_circ_20693,RMVar_hsa_circ_329748,RMVar_hsa_circ_359476,RMVar_hsa_circ_85860,RMVar_hsa_circ_115977,RMVar_hsa_circ_202571,RMVar_hsa_circ_202572,RMVar_hsa_circ_102996,RMVar_hsa_circ_112337,RMVar_hsa_circ_202573,RMVar_hsa_circ_202575,RMVar_hsa_circ_80879,RMVar_hsa_circ_202576,RMVar_hsa_circ_202574,RMVar_hsa_circ_128114,RMVar_hsa_circ_363398,RMVar_hsa_circ_104865,RMVar_hsa_circ_110641,RMVar_hsa_circ_88865,RMVar_hsa_circ_15296,RMVar_hsa_circ_106722,RMVar_hsa_circ_202577,RMVar_hsa_circ_202579,RMVar_hsa_circ_202580,RMVar_hsa_circ_202581,RMVar_hsa_circ_202578,RMVar_hsa_circ_122234,RMVar_hsa_circ_52700,RMVar_hsa_circ_66281,RMVar_hsa_circ_202582,RMVar_hsa_circ_202583,RMVar_hsa_circ_77394,RMVar_hsa_circ_360192,RMVar_hsa_circ_202584 34207 RMVar_ID_34207 Human_SNP_ID_87195283 A-to-I Human chr2 - 111851138 111851138 111851138 AGATCATGCCACTGTACTCCACCCACGGGAAAAGAGTGAGATCTTATCTCAAAAAAAAAAAAAAT AGATCATGCCACTGTACTCCACCCACGGGAAATGAGTGAGATCTTATCTCAAAAAAAAAAAAAAT T A ANAPC1 Ensembl:ENSG00000153107 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1375096865 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,RMVar_hsa_circ_91140,RMVar_hsa_circ_79739,RMVar_hsa_circ_115405,RMVar_hsa_circ_202535,RMVar_hsa_circ_111696,RMVar_hsa_circ_94820,RMVar_hsa_circ_202537,RMVar_hsa_circ_202538,RMVar_hsa_circ_202536,RMVar_hsa_circ_202539,RMVar_hsa_circ_126434,RMVar_hsa_circ_202540,RMVar_hsa_circ_110379,RMVar_hsa_circ_202547,RMVar_hsa_circ_100304,RMVar_hsa_circ_127752,RMVar_hsa_circ_202550,RMVar_hsa_circ_202549,RMVar_hsa_circ_121876,RMVar_hsa_circ_202551,RMVar_hsa_circ_115674,RMVar_hsa_circ_202556,RMVar_hsa_circ_105494,RMVar_hsa_circ_202558,RMVar_hsa_circ_114578,RMVar_hsa_circ_64008,RMVar_hsa_circ_65999,RMVar_hsa_circ_51456,RMVar_hsa_circ_76015,RMVar_hsa_circ_77552,RMVar_hsa_circ_117562,RMVar_hsa_circ_202562,RMVar_hsa_circ_87416,RMVar_hsa_circ_125054,RMVar_hsa_circ_202564,RMVar_hsa_circ_202565,RMVar_hsa_circ_202563,RMVar_hsa_circ_355552,RMVar_hsa_circ_81944,RMVar_hsa_circ_81374,RMVar_hsa_circ_202566,RMVar_hsa_circ_202568,RMVar_hsa_circ_202567,RMVar_hsa_circ_359476,RMVar_hsa_circ_85860,RMVar_hsa_circ_115977,RMVar_hsa_circ_202572,RMVar_hsa_circ_112337,RMVar_hsa_circ_202575,RMVar_hsa_circ_202576,RMVar_hsa_circ_128114,RMVar_hsa_circ_363398,RMVar_hsa_circ_104865,RMVar_hsa_circ_88865,RMVar_hsa_circ_15296,RMVar_hsa_circ_106722,RMVar_hsa_circ_202577,RMVar_hsa_circ_202579,RMVar_hsa_circ_202580,RMVar_hsa_circ_202578,RMVar_hsa_circ_122234,RMVar_hsa_circ_52700,RMVar_hsa_circ_202582,RMVar_hsa_circ_202583,RMVar_hsa_circ_77394,RMVar_hsa_circ_114328,RMVar_hsa_circ_327742,RMVar_hsa_circ_379032,RMVar_hsa_circ_202584,RMVar_hsa_circ_338664,RMVar_hsa_circ_115960,RMVar_hsa_circ_74937,RMVar_hsa_circ_202585,RMVar_hsa_circ_202586,RMVar_hsa_circ_295972,RMVar_hsa_circ_375905,RMVar_hsa_circ_202587 34208 RMVar_ID_34208 Human_SNP_ID_87200573 A-to-I Human chr2 - 111871546 111871546 111871546 GGGTTTCTCCATGTTAGTCATGCTGGTCTCGAACTCCCGACCTCAGGTGATCCACCCACCTTGGC GGGTTTCTCCATGTTAGTCATGCTGGTCTCGAGCTCCCGACCTCAGGTGATCCACCCACCTTGGC T C ANAPC1 Ensembl:ENSG00000153107 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1345257261 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,RMVar_hsa_circ_91140,RMVar_hsa_circ_115405,RMVar_hsa_circ_94820,RMVar_hsa_circ_202537,RMVar_hsa_circ_202538,RMVar_hsa_circ_202539,RMVar_hsa_circ_110379,RMVar_hsa_circ_202547,RMVar_hsa_circ_100304,RMVar_hsa_circ_202550,RMVar_hsa_circ_64008,RMVar_hsa_circ_65999,RMVar_hsa_circ_51456,RMVar_hsa_circ_87416,RMVar_hsa_circ_202565,RMVar_hsa_circ_355552,RMVar_hsa_circ_81374,RMVar_hsa_circ_359476,RMVar_hsa_circ_85860,RMVar_hsa_circ_202572,RMVar_hsa_circ_112337,RMVar_hsa_circ_202576,RMVar_hsa_circ_363398,RMVar_hsa_circ_104865,RMVar_hsa_circ_88865,RMVar_hsa_circ_8291,RMVar_hsa_circ_15296,RMVar_hsa_circ_106722,RMVar_hsa_circ_202577,RMVar_hsa_circ_202579,RMVar_hsa_circ_202578,RMVar_hsa_circ_202583,RMVar_hsa_circ_37575,RMVar_hsa_circ_34443,RMVar_hsa_circ_114328,RMVar_hsa_circ_379032,RMVar_hsa_circ_338664,RMVar_hsa_circ_115960,RMVar_hsa_circ_74937,RMVar_hsa_circ_202585,RMVar_hsa_circ_202586,RMVar_hsa_circ_375905,RMVar_hsa_circ_120087,RMVar_hsa_circ_202587,RMVar_hsa_circ_202588,RMVar_hsa_circ_358463,RMVar_hsa_circ_340531,RMVar_hsa_circ_364136,RMVar_hsa_circ_305364,RMVar_hsa_circ_79267,RMVar_hsa_circ_115832,RMVar_hsa_circ_202590,RMVar_hsa_circ_119960,RMVar_hsa_circ_101374,RMVar_hsa_circ_202594,RMVar_hsa_circ_202596,RMVar_hsa_circ_75939,RMVar_hsa_circ_202595,RMVar_hsa_circ_359636,RMVar_hsa_circ_69315,RMVar_hsa_circ_202598,RMVar_hsa_circ_89628,RMVar_hsa_circ_338111,RMVar_hsa_circ_202597,RMVar_hsa_circ_368863,RMVar_hsa_circ_105653,RMVar_hsa_circ_202599,RMVar_hsa_circ_202600 34209 RMVar_ID_34209 Human_SNP_ID_87218541 A-to-I Human chr2 - 111940524 111940524 111940524 CAGGAGCACCTGACACAGGATGCAGTTGCTAAAGCAAATCAAACAAAAGAGGGCTTGCCTGTTGC CAGGAGCACCTGACACAGGATGCAGTTGCTAAGGCAAATCAAACAAAAGAGGGCTTGCCTGTTGC T C RTRAFP1 Ensembl:ENSG00000225496 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879061438 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 34210 RMVar_ID_34210 Human_SNP_ID_87218542 A-to-I Human chr2 - 111940524 111940524 111940524 CAGGAGCACCTGACACAGGATGCAGTTGCTAAAGCAAATCAAACAAAAGAGGGCTTGCCTGTTGC CAGGAGCACCTGACACAGGATGCAGTTGCTAACGCAAATCAAACAAAAGAGGGCTTGCCTGTTGC T G RTRAFP1 Ensembl:ENSG00000225496 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879061438 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 34211 RMVar_ID_34211 Human_SNP_ID_87218546 A-to-I Human chr2 - 111940549 111940549 111940549 GCTTAAGGCAATTCAAATTTTGGTTCAGGAGCACCTGACACAGGATGCAGTTGCTAAAGCAAATC GCTTAAGGCAATTCAAATTTTGGTTCAGGAGCGCCTGACACAGGATGCAGTTGCTAAAGCAAATC T C RTRAFP1 Ensembl:ENSG00000225496 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879034985 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1842600,Human_miRNA_ID_1905169,Human_miRNA_ID_2234008,Human_miRNA_ID_2234009,Human_miRNA_ID_2234010,Human_miRNA_ID_3028164,Human_miRNA_ID_3028165,Human_miRNA_ID_3028166 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 34212 RMVar_ID_34212 Human_SNP_ID_87218548 A-to-I Human chr2 - 111940566 111940566 111940566 GATGATTGCCTGGTAATGCTTAAGGCAATTCAAATTTTGGTTCAGGAGCACCTGACACAGGATGC GATGATTGCCTGGTAATGCTTAAGGCAATTCAGATTTTGGTTCAGGAGCACCTGACACAGGATGC T C RTRAFP1 Ensembl:ENSG00000225496 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878984879 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 34213 RMVar_ID_34213 Human_SNP_ID_87218549 A-to-I Human chr2 - 111940567 111940567 111940567 TGATGATTGCCTGGTAATGCTTAAGGCAATTCAAATTTTGGTTCAGGAGCACCTGACACAGGATG TGATGATTGCCTGGTAATGCTTAAGGCAATTCGAATTTTGGTTCAGGAGCACCTGACACAGGATG T C RTRAFP1 Ensembl:ENSG00000225496 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878909145 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 34214 RMVar_ID_34214 Human_SNP_ID_87236565 A-to-I Human chr2 + 112014901 112014901 112014901 CCTTAAATGATCCACCCGCTTTGGCCTCCCAAAATGCTGGGATTACAGGTGTGAGCCACTGCACC CCTTAAATGATCCACCCGCTTTGGCCTCCCAATATGCTGGGATTACAGGTGTGAGCCACTGCACC A T MERTK Ensembl:ENSG00000153208 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934089374 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_373259,RMVar_hsa_circ_202606,RMVar_hsa_circ_72269,RMVar_hsa_circ_57726,RMVar_hsa_circ_91189,RMVar_hsa_circ_202610,RMVar_hsa_circ_53190 34215 RMVar_ID_34215 Human_SNP_ID_87284823 A-to-I Human chr2 - 112213093 112213093 112213093 TGGAGGTGCATACCTGGAGTCCCAGCTACTTGAGAGTCTGAGGCAAGAGGATCACTGGAGCCCAT TGGAGGTGCATACCTGGAGTCCCAGCTACTTGGGAGTCTGAGGCAAGAGGATCACTGGAGCCCAT T C ZC3H8 Ensembl:ENSG00000144161 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs549756970 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 34216 RMVar_ID_34216 Human_SNP_ID_87292753 A-to-I Human chr2 - 112249592 112249592 112249592 AAATACAAAAAAATTTAGCCAGGCATGGTGGCATGCACCTGTAGTCCCAGCTACTAGGGAGGCTG AAATACAAAAAAATTTAGCCAGGCATGGTGGCCTGCACCTGTAGTCCCAGCTACTAGGGAGGCTG T G ZC3H8 Ensembl:ENSG00000144161 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1309181447 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 34217 RMVar_ID_34217 Human_SNP_ID_87306686 A-to-I Human chr2 + 112308548 112308548 112308548 CACCTCCTGGATTCAAGCAGTTCTCCTGCCTCAGACTCCTGAGTAGCTGAGACTACAGGTGTATG CACCTCCTGGATTCAAGCAGTTCTCCTGCCTCCGACTCCTGAGTAGCTGAGACTACAGGTGTATG A C ZC3H6 Ensembl:ENSG00000188177 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1394454896 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118236,RMVar_hsa_circ_59090,RMVar_hsa_circ_271068,RMVar_hsa_circ_340045,RMVar_hsa_circ_357555,RMVar_hsa_circ_323132,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_32356,RMVar_hsa_circ_73197,RMVar_hsa_circ_202632,RMVar_hsa_circ_202633 34218 RMVar_ID_34218 Human_SNP_ID_87313373 A-to-I Human chr2 + 112338895 112338853 112338895 ATATATATATATATATATATATATATATATATATATATATATATATATATAATTTTTTTTTTTTG _________________________________TATATATATATATATATAATTTTTTTTTTTTG GTGTATATATATATATATATATATATATATATATATATATATA G ZC3H6 Ensembl:ENSG00000188177 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs778683215 Functional Loss DEL dbSNP153 1..33 33 - - - RMVar_hsa_circ_118236,RMVar_hsa_circ_269195,RMVar_hsa_circ_202633 34219 RMVar_ID_34219 Human_SNP_ID_87313377 A-to-I Human chr2 + 112338893 112338853 112338893 ATATATATATATATATATATATATATATATATATATATATATATATATATATAATTTTTTTTTTT _________________________________TATATATATATATATATATAATTTTTTTTTTT GTGTATATATATATATATATATATATATATATATATATATA G ZC3H6 Ensembl:ENSG00000188177 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1349770101 Functional Loss DEL dbSNP153 1..33 33 - - - RMVar_hsa_circ_118236,RMVar_hsa_circ_269195,RMVar_hsa_circ_202633 34220 RMVar_ID_34220 Human_SNP_ID_87313436 A-to-I Human chr2 + 112338893 112338880 112338893 ATATATATATATATATATATATATATATATATATATATATATATATATATATAATTTTTTTTTTT ATATATATATATATATATAT_____________TATATATATATATATATATAATTTTTTTTTTT TATATATATATATA T ZC3H6 Ensembl:ENSG00000188177 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1553497344 Functional Loss DEL dbSNP153 21..33 33 - - - RMVar_hsa_circ_118236,RMVar_hsa_circ_269195,RMVar_hsa_circ_202633 34221 RMVar_ID_34221 Human_SNP_ID_87313450 A-to-I Human chr2 + 112338887 112338887 112338887 GTATATATATATATATATATATATATATATATATATATATATATATATATATATATATAATTTTT GTATATATATATATATATATATATATATATATGTATATATATATATATATATATATATAATTTTT A G ZC3H6 Ensembl:ENSG00000188177 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs188338519 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118236,RMVar_hsa_circ_269195,RMVar_hsa_circ_202633 34222 RMVar_ID_34222 Human_SNP_ID_87313461 A-to-I Human chr2 + 112338893 112338893 112338893 ATATATATATATATATATATATATATATATATATATATATATATATATATATAATTTTTTTTTTT ATATATATATATATATATATATATATATATATGTATATATATATATATATATAATTTTTTTTTTT A G ZC3H6 Ensembl:ENSG00000188177 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs181245972 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118236,RMVar_hsa_circ_269195,RMVar_hsa_circ_202633 34223 RMVar_ID_34223 Human_SNP_ID_87313463 A-to-I Human chr2 + 112338895 112338895 112338895 ATATATATATATATATATATATATATATATATATATATATATATATATATAATTTTTTTTTTTTG ATATATATATATATATATATATATATATATATGTATATATATATATATATAATTTTTTTTTTTTG A G ZC3H6 Ensembl:ENSG00000188177 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs186600900 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118236,RMVar_hsa_circ_269195,RMVar_hsa_circ_202633 34224 RMVar_ID_34224 Human_SNP_ID_87346084 A-to-I Human chr2 - 112477452 112477452 112477452 ATTGCCCGAGGTTAGGAGTTCGAGACCAGTCTAGGCAACATGGTGAAACCCCAGTTCTACTAAAA ATTGCCCGAGGTTAGGAGTTCGAGACCAGTCTGGGCAACATGGTGAAACCCCAGTTCTACTAAAA T C HSALNG0017963 RNACentral:URS0000E95A39 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1261913501 Functional Loss SNV dbSNP153 33..33 33 - - - 34225 RMVar_ID_34225 Human_SNP_ID_87349069 A-to-I Human chr2 + 112488533 112488533 112488533 TAATCTCAGCACTTTGGGAGTCTGAGGCGGACAGATCACTTAGGGTCAGGAGTTCGAGACCAATC TAATCTCAGCACTTTGGGAGTCTGAGGCGGACGGATCACTTAGGGTCAGGAGTTCGAGACCAATC A G TTL Ensembl:ENSG00000114999 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1442064613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13580697 RMVar_hsa_circ_76778,RMVar_hsa_circ_288797,RMVar_hsa_circ_297838,RMVar_hsa_circ_294726,RMVar_hsa_circ_275470,RMVar_hsa_circ_202644,RMVar_hsa_circ_202646,RMVar_hsa_circ_202647,RMVar_hsa_circ_202645,RMVar_hsa_circ_202643 34226 RMVar_ID_34226 Human_SNP_ID_87354070 A-to-I Human chr2 + 112511839 112511839 112511839 GCAATCTACACACTTCAGCCTCCCAGAGTGCTAGGATTACAGGCGTGAGCCACCATGCCCAGCCA GCAATCTACACACTTCAGCCTCCCAGAGTGCTGGGATTACAGGCGTGAGCCACCATGCCCAGCCA A G TTL Ensembl:ENSG00000114999 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1428403599 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76778,RMVar_hsa_circ_294726,RMVar_hsa_circ_202646,RMVar_hsa_circ_202647,RMVar_hsa_circ_202652,RMVar_hsa_circ_202648,RMVar_hsa_circ_110966,RMVar_hsa_circ_24854,RMVar_hsa_circ_94831,RMVar_hsa_circ_284617,RMVar_hsa_circ_202653 34227 RMVar_ID_34227 Human_SNP_ID_87358748 A-to-I Human chr2 + 112531083 112531083 112531083 CACACTGCAGCCTCGAATTTCTGGGCTTGAGCAGTCCTCCCGTCTCAGCCTCCTGAGTAGCTGAG CACACTGCAGCCTCGAATTTCTGGGCTTGAGCGGTCCTCCCGTCTCAGCCTCCTGAGTAGCTGAG A G TTL Ensembl:ENSG00000114999 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1397572891 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8202993,Human_RBP_ID_13581076,Human_RBP_ID_26475961 Human_miRNA_ID_2709579,Human_miRNA_ID_2712706,Human_miRNA_ID_3048686 RMVar_hsa_circ_76778,RMVar_hsa_circ_202647,RMVar_hsa_circ_202648,RMVar_hsa_circ_110966,RMVar_hsa_circ_94831,RMVar_hsa_circ_202653 34228 RMVar_ID_34228 Human_SNP_ID_87361839 A-to-I Human chr2 + 112543978 112543978 112543978 GGTGGTGCGCACCCAAGTAGCTGGTCCCAGCTACTCGGGAGGCTGAGGTGGGAGGATAAGTTGAA GGTGGTGCGCACCCAAGTAGCTGGTCCCAGCTTCTCGGGAGGCTGAGGTGGGAGGATAAGTTGAA A T POLR1B Ensembl:ENSG00000125630 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1037148770 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25579868 34229 RMVar_ID_34229 Human_SNP_ID_87363049 A-to-I Human chr2 + 112548656 112548656 112548656 TTTTTTTGAGACGGAGTCTCCCTCTCTCACCCAGGTTGGAGCGCAGTGGCGCAATCTTGGCTCAC TTTTTTTGAGACGGAGTCTCCCTCTCTCACCCCGGTTGGAGCGCAGTGGCGCAATCTTGGCTCAC A C POLR1B Ensembl:ENSG00000125630 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1158515225 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47061,RMVar_hsa_circ_318754,RMVar_hsa_circ_354029,RMVar_hsa_circ_357081,RMVar_hsa_circ_326716,RMVar_hsa_circ_284203,RMVar_hsa_circ_273163,RMVar_hsa_circ_202656,RMVar_hsa_circ_202657,RMVar_hsa_circ_82908,RMVar_hsa_circ_202659 34230 RMVar_ID_34230 Human_SNP_ID_87364689 A-to-I Human chr2 + 112555385 112555385 112555385 AAAAAACACCTGGTGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGGGGTGGGAGG AAAAAACACCTGGTGCGGTGGCTCACACCTGTCATCCCAGCACTTTGGGAGGCCGGGGTGGGAGG A C POLR1B Ensembl:ENSG00000125630 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs535674929 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47061,RMVar_hsa_circ_318754,RMVar_hsa_circ_354029,RMVar_hsa_circ_326716,RMVar_hsa_circ_284203,RMVar_hsa_circ_202657,RMVar_hsa_circ_82908,RMVar_hsa_circ_202659,RMVar_hsa_circ_72184,RMVar_hsa_circ_349647,RMVar_hsa_circ_202660,RMVar_hsa_circ_318447,RMVar_hsa_circ_344553 34231 RMVar_ID_34231 Human_SNP_ID_87365229 A-to-I Human chr2 + 112557702 112557702 112557702 GGACTCAAGCGATCCTTCCGCCTCAGCCTCCCAAGTAGCTGGAACTACAGGCACGCCCCACCCCC GGACTCAAGCGATCCTTCCGCCTCAGCCTCCCGAGTAGCTGGAACTACAGGCACGCCCCACCCCC A G POLR1B Ensembl:ENSG00000125630 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs902547870 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47061,RMVar_hsa_circ_318754,RMVar_hsa_circ_354029,RMVar_hsa_circ_326716,RMVar_hsa_circ_284203,RMVar_hsa_circ_202657,RMVar_hsa_circ_82908,RMVar_hsa_circ_202659,RMVar_hsa_circ_72184,RMVar_hsa_circ_349647,RMVar_hsa_circ_202660,RMVar_hsa_circ_318447,RMVar_hsa_circ_344553 34232 RMVar_ID_34232 Human_SNP_ID_87366306 A-to-I Human chr2 + 112561872 112561872 112561872 GTTTGTTTGTTTTGTAGAGATGGGGTCTTGCTATGTTATCCAGGCTGGTCTCGAACTCCTGGCCT GTTTGTTTGTTTTGTAGAGATGGGGTCTTGCTGTGTTATCCAGGCTGGTCTCGAACTCCTGGCCT A G POLR1B Ensembl:ENSG00000125630 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs769187876 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47061,RMVar_hsa_circ_326716,RMVar_hsa_circ_284203,RMVar_hsa_circ_82908,RMVar_hsa_circ_202659,RMVar_hsa_circ_72184,RMVar_hsa_circ_14682,RMVar_hsa_circ_344553,RMVar_hsa_circ_202664,RMVar_hsa_circ_48357,RMVar_hsa_circ_87156,RMVar_hsa_circ_373003,RMVar_hsa_circ_202665 34233 RMVar_ID_34233 Human_SNP_ID_87369910 A-to-I Human chr2 + 112576837 112576837 112576837 CCCACCTCGGCCTCCGAAAGTGCTAGGATTACAGGTGTGAGCCACTGTGCCTGGCCTCCGGTGAG CCCACCTCGGCCTCCGAAAGTGCTAGGATTACTGGTGTGAGCCACTGTGCCTGGCCTCCGGTGAG A T POLR1B Ensembl:ENSG00000125630 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1259136136 Functional Loss SNV dbSNP153 33..33 33 - - - 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 34234 RMVar_ID_34234 Human_SNP_ID_87371076 A-to-I Human chr2 + 112581555 112581555 112581555 ACTGCAGGCCAGGCGCTGTGGCTCATACCTGTAATCTCAGCACTTTGGGAGGCCGACATGGGCGG ACTGCAGGCCAGGCGCTGTGGCTCATACCTGTCATCTCAGCACTTTGGGAGGCCGACATGGGCGG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs937426304 Functional Loss SNV dbSNP153 33..33 33 - - - 34235 RMVar_ID_34235 Human_SNP_ID_87371077 A-to-I Human chr2 + 112581555 112581555 112581555 ACTGCAGGCCAGGCGCTGTGGCTCATACCTGTAATCTCAGCACTTTGGGAGGCCGACATGGGCGG ACTGCAGGCCAGGCGCTGTGGCTCATACCTGTGATCTCAGCACTTTGGGAGGCCGACATGGGCGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs937426304 Functional Loss SNV dbSNP153 33..33 33 - - - 34236 RMVar_ID_34236 Human_SNP_ID_87374741 A-to-I Human chr2 + 112595435 112595435 112595435 CAATATGTTGGCCAGGCTGGTCTAGAACTCCTAACCTCAAGTGATCTGCCCTCGTCTGCCTCCCA CAATATGTTGGCCAGGCTGGTCTAGAACTCCTGACCTCAAGTGATCTGCCCTCGTCTGCCTCCCA A G AC012442.3 Ensembl:ENSG00000243389 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1051669769 Functional Loss SNV dbSNP153 33..33 33 - - - 34237 RMVar_ID_34237 Human_SNP_ID_87374749 A-to-I Human chr2 + 112595467 112595467 112595467 AACCTCAAGTGATCTGCCCTCGTCTGCCTCCCAAAGTGCTGGGATTCCAGGCGTGAGCCACCACA AACCTCAAGTGATCTGCCCTCGTCTGCCTCCCGAAGTGCTGGGATTCCAGGCGTGAGCCACCACA A G AC012442.3 Ensembl:ENSG00000243389 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1416612604 Functional Loss SNV dbSNP153 33..33 33 - - - 34238 RMVar_ID_34238 Human_SNP_ID_87375473 A-to-I Human chr2 + 112598240 112598240 112598240 AAAATGTAGGCCAGGCGCAGTGGCTCACACCTATAATCCCAGCACTTTGGGAGGCCGAGGCCGGC AAAATGTAGGCCAGGCGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGCCGGC A G AC012442.3 Ensembl:ENSG00000243389 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1229717781 Functional Loss SNV dbSNP153 33..33 33 - - - 34239 RMVar_ID_34239 Human_SNP_ID_87386407 A-to-I Human chr2 + 112642546 112642546 112642546 TGTTGATAGGCTGGTCTCGAACTCCCGTCCTCAGGTGATCCACCCGCCTTGGCCTCCCAAAATGC TGTTGATAGGCTGGTCTCGAACTCCCGTCCTCGGGTGATCCACCCGCCTTGGCCTCCCAAAATGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs975051355 Functional Loss SNV dbSNP153 33..33 33 - - - 34240 RMVar_ID_34240 Human_SNP_ID_87389486 A-to-I Human chr2 + 112653848 112653848 112653848 CAGTTTTGCTCTTGTTGCCCAGGCTGGAGTGCAATGGCATGATCTTGGCTCACCACAACCTCTAC CAGTTTTGCTCTTGTTGCCCAGGCTGGAGTGCGATGGCATGATCTTGGCTCACCACAACCTCTAC A G SLC20A1 Ensembl:ENSG00000144136 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1226598040 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15322,RMVar_hsa_circ_122313,RMVar_hsa_circ_202672,RMVar_hsa_circ_81535,RMVar_hsa_circ_202671,RMVar_hsa_circ_202673,RMVar_hsa_circ_126614,RMVar_hsa_circ_27779,RMVar_hsa_circ_39219 34241 RMVar_ID_34241 Human_SNP_ID_87389690 A-to-I Human chr2 + 112654633 112654633 112654633 GAATTGTAGTTTGGGGCCGGGCGCGGTGGCTCATGCTTGTAATCCCAGCACTTTGGGAGGCCGAG GAATTGTAGTTTGGGGCCGGGCGCGGTGGCTCGTGCTTGTAATCCCAGCACTTTGGGAGGCCGAG A G SLC20A1 Ensembl:ENSG00000144136 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1312266523 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15322,RMVar_hsa_circ_122313,RMVar_hsa_circ_202672,RMVar_hsa_circ_81535,RMVar_hsa_circ_202671,RMVar_hsa_circ_202673,RMVar_hsa_circ_126614,RMVar_hsa_circ_27779,RMVar_hsa_circ_39219 34242 RMVar_ID_34242 Human_SNP_ID_87389849 A-to-I Human chr2 + 112655134 112655134 112655134 GGGATTACACATGTGCATCACCACGCCCAGCTAATTTTTGTATTTTTAGTAGATACGTGGTTTCA GGGATTACACATGTGCATCACCACGCCCAGCTGATTTTTGTATTTTTAGTAGATACGTGGTTTCA A G SLC20A1 Ensembl:ENSG00000144136 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1271626379 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13582395 RMVar_hsa_circ_15322,RMVar_hsa_circ_122313,RMVar_hsa_circ_202672,RMVar_hsa_circ_81535,RMVar_hsa_circ_202671,RMVar_hsa_circ_202673,RMVar_hsa_circ_126614,RMVar_hsa_circ_27779,RMVar_hsa_circ_39219 34243 RMVar_ID_34243 Human_SNP_ID_87389852 A-to-I Human chr2 + 112655152 112655152 112655152 CACCACGCCCAGCTAATTTTTGTATTTTTAGTAGATACGTGGTTTCACCGTGTTGGTCAGTCTGG CACCACGCCCAGCTAATTTTTGTATTTTTAGTGGATACGTGGTTTCACCGTGTTGGTCAGTCTGG A G SLC20A1 Ensembl:ENSG00000144136 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs371662719 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13582396 RMVar_hsa_circ_15322,RMVar_hsa_circ_122313,RMVar_hsa_circ_202672,RMVar_hsa_circ_81535,RMVar_hsa_circ_202671,RMVar_hsa_circ_202673,RMVar_hsa_circ_126614,RMVar_hsa_circ_27779,RMVar_hsa_circ_39219 34244 RMVar_ID_34244 Human_SNP_ID_87389880 A-to-I Human chr2 + 112655245 112655245 112655245 CGGACCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCTGCCGCGTCTGGCCTTGTGTCTG CGGACCTCAGCCTCCCAAAGTGCTGGGATTACGGGCGTGAGCTGCCGCGTCTGGCCTTGTGTCTG A G SLC20A1 Ensembl:ENSG00000144136 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1212463728 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15322,RMVar_hsa_circ_122313,RMVar_hsa_circ_202672,RMVar_hsa_circ_81535,RMVar_hsa_circ_202671,RMVar_hsa_circ_202673,RMVar_hsa_circ_126614,RMVar_hsa_circ_27779,RMVar_hsa_circ_39219 34245 RMVar_ID_34245 Human_SNP_ID_87390210 A-to-I Human chr2 + 112656314 112656314 112656314 GCCCTGCCAGGTTCAAGTGATTCTCCCACCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCCA GCCCTGCCAGGTTCAAGTGATTCTCCCACCTCCGCCTCCCGAGTAGCTGGGACTACAGGCGCCCA A C SLC20A1 Ensembl:ENSG00000144136 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1431873624 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15322,RMVar_hsa_circ_122313,RMVar_hsa_circ_202672,RMVar_hsa_circ_81535,RMVar_hsa_circ_202671,RMVar_hsa_circ_202673,RMVar_hsa_circ_126614,RMVar_hsa_circ_27779,RMVar_hsa_circ_39219 34246 RMVar_ID_34246 Human_SNP_ID_87390973 A-to-I Human chr2 + 112659036 112659036 112659036 AAACTTGGAGATTTGGAGGAAGCTCCAGAGAGAGAGAGGCTTCCCAGCGTGGACTTGAAAGAGGA AAACTTGGAGATTTGGAGGAAGCTCCAGAGAGCGAGAGGCTTCCCAGCGTGGACTTGAAAGAGGA A C SLC20A1 Ensembl:ENSG00000144136 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1296654092 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_922630,Human_RBP_ID_17965488,Human_RBP_ID_19000055,Human_RBP_ID_22765120,Human_RBP_ID_23115052,Human_RBP_ID_26339752,Human_RBP_ID_26487384 Human_Splice_Rec_289251,Human_Splice_Rec_289271,Human_Splice_Rec_289278,Human_Splice_Rec_289279,Human_Splice_Rec_289294,Human_Splice_Rec_289295,Human_Splice_Rec_289303 Human_miRNA_ID_3003246 RMVar_hsa_circ_15322,RMVar_hsa_circ_202672,RMVar_hsa_circ_81535,RMVar_hsa_circ_202673,RMVar_hsa_circ_126614,RMVar_hsa_circ_27779,RMVar_hsa_circ_39219,RMVar_hsa_circ_266720,RMVar_hsa_circ_357025,RMVar_hsa_circ_358731 34247 RMVar_ID_34247 Human_SNP_ID_87391731 A-to-I Human chr2 + 112661749 112661749 112661749 TTTTGTATTTTTAGTAGACACAGGATTTCACCATGTTGGCCAAGCTGGTCATGAACTCCTAACCT TTTTGTATTTTTAGTAGACACAGGATTTCACCGTGTTGGCCAAGCTGGTCATGAACTCCTAACCT A G SLC20A1 Ensembl:ENSG00000144136 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs999200638 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_202672,RMVar_hsa_circ_81535,RMVar_hsa_circ_202673,RMVar_hsa_circ_126614,RMVar_hsa_circ_202677,RMVar_hsa_circ_116745,RMVar_hsa_circ_202678 34248 RMVar_ID_34248 Human_SNP_ID_87412048 A-to-I Human chr2 - 112739382 112739382 112739382 GGGTCTTGCCATGTTGCCCAGACTGGAGTACAATGGCATAATCATAGCTCACTGCAGCCTTGACC GGGTCTTGCCATGTTGCCCAGACTGGAGTACAGTGGCATAATCATAGCTCACTGCAGCCTTGACC T C CKAP2L Ensembl:ENSG00000169607 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042203905 Functional Loss SNV dbSNP153 33..33 33 - - - 34249 RMVar_ID_34249 Human_SNP_ID_87412144 A-to-I Human chr2 - 112739815 112739815 112739815 ACCCCAACTCTATGAAAAATAAAAAATTAGCCAGGCATGCTGGCATACGTTTGTGCTCCCACCAG ACCCCAACTCTATGAAAAATAAAAAATTAGCCTGGCATGCTGGCATACGTTTGTGCTCCCACCAG T A CKAP2L Ensembl:ENSG00000169607 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs764241555 Functional Loss SNV dbSNP153 33..33 33 - - - 34250 RMVar_ID_34250 Human_SNP_ID_87519754 A-to-I Human chr2 + 113187726 113187726 113187726 TTCATTATCCAAGTGACACAGGAAGTTGAACCAGTAAGCAGGAGTCATCATAATATGAAAACGTT TTCATTATCCAAGTGACACAGGAAGTTGAACCGGTAAGCAGGAGTCATCATAATATGAAAACGTT A G PSD4 Ensembl:ENSG00000125637 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs147381695 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19024,RMVar_hsa_circ_80791,RMVar_hsa_circ_73174,RMVar_hsa_circ_202684 34251 RMVar_ID_34251 Human_SNP_ID_87520633 A-to-I Human chr2 + 113191639 113191639 113191639 CCAGTTCAACTTCCTAATTGTATCACTTGAATAATGAATGTTTAAATAACTGGAATACCCCACAC CCAGTTCAACTTCCTAATTGTATCACTTGAATGATGAATGTTTAAATAACTGGAATACCCCACAC A G PSD4 Ensembl:ENSG00000125637 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs913104212 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19024,RMVar_hsa_circ_80791,RMVar_hsa_circ_73174,RMVar_hsa_circ_202684 34252 RMVar_ID_34252 Human_SNP_ID_87584472 A-to-I Human chr2 + 113469317 113469317 113469317 GGTGTGCACCACCACACCCAGCTAATTTTTGTATTTTTAGTAGAGACGGTTTCGCCACATTGGCC GGTGTGCACCACCACACCCAGCTAATTTTTGTGTTTTTAGTAGAGACGGTTTCGCCACATTGGCC A G CBWD2 Ensembl:ENSG00000136682 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs903895304 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3738,RMVar_hsa_circ_75294,RMVar_hsa_circ_312678,RMVar_hsa_circ_342882,RMVar_hsa_circ_22758,RMVar_hsa_circ_352902 34253 RMVar_ID_34253 Human_SNP_ID_87616407 A-to-I Human chr2 + 113595400 113595400 113595400 GGTGTTCTCCAGTGCCAAGTACCCTGCTCCAGAGCGCCTGCAGGAATATGGCTCCATCTTCACGG GGTGTTCTCCAGTGCCAAGTACCCTGCTCCAGGGCGCCTGCAGGAATATGGCTCCATCTTCACGG A G WASH2P Ensembl:ENSG00000146556 Pseudogene exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs879998894 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_290418,Human_Splice_Rec_290434 Human_miRNA_ID_1887415,Human_miRNA_ID_1887416 34254 RMVar_ID_34254 Human_SNP_ID_87616517 A-to-I Human chr2 - 113595713 113595713 113595713 TCCTCGGGCTCCGGCTTGGTGCTCACGCACACAGGAAAGTCCTTCAGCTTCTCCTGGGAGGGCCA TCCTCGGGCTCCGGCTTGGTGCTCACGCACACGGGAAAGTCCTTCAGCTTCTCCTGGGAGGGCCA T C lnc-SLC35F5-17 RNACentral:URS00008BF43D lincRNA intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs773670713 Functional Loss SNV dbSNP153 33..33 33 - - - 34255 RMVar_ID_34255 Human_SNP_ID_87616733 A-to-I Human chr2 - 113596386 113596386 113596386 TGGCCCAGGTCTGGCACATAGAAGTAGTTCTCAGGGACCTGCAAGATTAGGCAGGGACATGTGAG TGGCCCAGGTCTGGCACATAGAAGTAGTTCTCTGGGACCTGCAAGATTAGGCAGGGACATGTGAG T A lnc-SLC35F5-17 RNACentral:URS00008BF43D lincRNA intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs2592653 Functional Loss SNV dbSNP153 33..33 33 - - - 34256 RMVar_ID_34256 Human_SNP_ID_87617985 A-to-I Human chr2 - 113599773 113599773 113599773 CATTAGTGCCCGTTGGAGAAAACGGGAATCCCAAAGAAATGGTGGGTCCTGGCCATCCGTGAGAT CATTAGTGCCCGTTGGAGAAAACGGGAATCCCGAAGAAATGGTGGGTCCTGGCCATCCGTGAGAT T C DDX11L2 Ensembl:ENSG00000236397 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs67465876 Functional Loss SNV dbSNP153 33..33 33 - - - 34257 RMVar_ID_34257 Human_SNP_ID_87619147 A-to-I Human chr2 - 113602484 113602484 113602484 CCGAGTTGTCACAAAGCCAGGCAGTGGCCCCAACCTCTGTGCTTAGGGGAATGCTGCTCCACCTT CCGAGTTGTCACAAAGCCAGGCAGTGGCCCCACCCTCTGTGCTTAGGGGAATGCTGCTCCACCTT T G lnc-SLC35F5-16 RNACentral:URS00008BD7F6 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1414177991 Functional Loss SNV dbSNP153 33..33 33 - - - 34258 RMVar_ID_34258 Human_SNP_ID_87630185 A-to-I Human chr2 + 113639646 113639646 113639646 CAAGACTCCATATATGGAGATCCCTTGAGATCAAGAGTTCGAGACCAGCCTGGCCAACACGGCAA CAAGACTCCATATATGGAGATCCCTTGAGATCGAGAGTTCGAGACCAGCCTGGCCAACACGGCAA A G RABL2A Ensembl:ENSG00000144134 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1203052517 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5054 34259 RMVar_ID_34259 Human_SNP_ID_87630442 A-to-I Human chr2 + 113640586 113640586 113640586 TTTAGTAGAGACGGAATTTCACCATGTTGGCCAGGCTGGTCTCAAACTCCTGACCTCAGGTGATT TTTAGTAGAGACGGAATTTCACCATGTTGGCCCGGCTGGTCTCAAACTCCTGACCTCAGGTGATT A C RABL2A Ensembl:ENSG00000144134 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1433005486 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5054 34260 RMVar_ID_34260 Human_SNP_ID_87647178 A-to-I Human chr2 - 113707698 113707698 113707698 AAAATTAGCCAGGCATGGTGGTGCACGCCTGTAGTCCCAGCTACTTGTGAGGCTGAGGTAGGAGA AAAATTAGCCAGGCATGGTGGTGCACGCCTGTCGTCCCAGCTACTTGTGAGGCTGAGGTAGGAGA T G SLC35F5 Ensembl:ENSG00000115084 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs142753958 Functional Loss SNV dbSNP153 33..33 33 - - - 34261 RMVar_ID_34261 Human_SNP_ID_87647333 A-to-I Human chr2 - 113708487 113708484 113708487 TTGGCCAGGTTGGTCTTGAACTCTTGACCTCAAGTGATCTACACGCCTCGGCCTCCCAAAGTGCT TTGGCCAGGTTGGTCTTGAACTCTTGACCTCA___GATCTACACGCCTCGGCCTCCCAAAGTGCT CACT C SLC35F5 Ensembl:ENSG00000115084 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1313085698 Functional Loss DEL dbSNP153 33..35 33 - - - 34262 RMVar_ID_34262 Human_SNP_ID_87647340 A-to-I Human chr2 - 113708501 113708501 113708501 GAGGTTTTACCATGTTGGCCAGGTTGGTCTTGAACTCTTGACCTCAAGTGATCTACACGCCTCGG GAGGTTTTACCATGTTGGCCAGGTTGGTCTTGGACTCTTGACCTCAAGTGATCTACACGCCTCGG T C SLC35F5 Ensembl:ENSG00000115084 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1480297834 Functional Loss SNV dbSNP153 33..33 33 - - - 34263 RMVar_ID_34263 Human_SNP_ID_87647344 A-to-I Human chr2 - 113708513 113708513 113708513 TATAGTAGAGAGGAGGTTTTACCATGTTGGCCAGGTTGGTCTTGAACTCTTGACCTCAAGTGATC TATAGTAGAGAGGAGGTTTTACCATGTTGGCCTGGTTGGTCTTGAACTCTTGACCTCAAGTGATC T A SLC35F5 Ensembl:ENSG00000115084 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1444201370 Functional Loss SNV dbSNP153 33..33 33 - - - 34264 RMVar_ID_34264 Human_SNP_ID_87647346 A-to-I Human chr2 - 113708522 113708522 113708522 TTTTGTATTTATAGTAGAGAGGAGGTTTTACCATGTTGGCCAGGTTGGTCTTGAACTCTTGACCT TTTTGTATTTATAGTAGAGAGGAGGTTTTACCGTGTTGGCCAGGTTGGTCTTGAACTCTTGACCT T C SLC35F5 Ensembl:ENSG00000115084 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1208037336 Functional Loss SNV dbSNP153 33..33 33 - - - 34265 RMVar_ID_34265 Human_SNP_ID_87647349 A-to-I Human chr2 - 113708537 113708533 113708537 CACGCCCAGCTAATTTTTTGTATTTATAGTAGAGAGGAGGTTTTACCATGTTGGCCAGGTTGGTC CACGCCCAGCTAATTTTTTGTATTTATAGTAG____GAGGTTTTACCATGTTGGCCAGGTTGGTC CCTCT C SLC35F5 Ensembl:ENSG00000115084 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1219563737 Functional Loss DEL dbSNP153 33..36 33 - - - 34266 RMVar_ID_34266 Human_SNP_ID_87647351 A-to-I Human chr2 - 113708537 113708537 113708537 CACGCCCAGCTAATTTTTTGTATTTATAGTAGAGAGGAGGTTTTACCATGTTGGCCAGGTTGGTC CACGCCCAGCTAATTTTTTGTATTTATAGTAGGGAGGAGGTTTTACCATGTTGGCCAGGTTGGTC T C SLC35F5 Ensembl:ENSG00000115084 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1318951262 Functional Loss SNV dbSNP153 33..33 33 - - - 34267 RMVar_ID_34267 Human_SNP_ID_87647354 A-to-I Human chr2 - 113708548 113708548 113708548 ACATGCACCACCACGCCCAGCTAATTTTTTGTATTTATAGTAGAGAGGAGGTTTTACCATGTTGG ACATGCACCACCACGCCCAGCTAATTTTTTGTGTTTATAGTAGAGAGGAGGTTTTACCATGTTGG T C SLC35F5 Ensembl:ENSG00000115084 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs961786962 Functional Loss SNV dbSNP153 33..33 33 - - - 34268 RMVar_ID_34268 Human_SNP_ID_87647361 A-to-I Human chr2 - 113708594 113708594 113708594 TCAAGTGATTCTCCTGCCTCAGCCTCCCGAATAGCTGGGATTACAGACATGCACCACCACGCCCA TCAAGTGATTCTCCTGCCTCAGCCTCCCGAATGGCTGGGATTACAGACATGCACCACCACGCCCA T C SLC35F5 Ensembl:ENSG00000115084 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1292433447 Functional Loss SNV dbSNP153 33..33 33 - - - 34269 RMVar_ID_34269 Human_SNP_ID_87647392 A-to-I Human chr2 - 113708680 113708680 113708680 TTTTTTTGAGACAGAGTCTCACTCCATTGCCCAGGCTGAAGTGCAGTGGCACGATCTCGGCTCAC TTTTTTTGAGACAGAGTCTCACTCCATTGCCCCGGCTGAAGTGCAGTGGCACGATCTCGGCTCAC T G SLC35F5 Ensembl:ENSG00000115084 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1470295097 Functional Loss SNV dbSNP153 33..33 33 - - - 34270 RMVar_ID_34270 Human_SNP_ID_87647395 A-to-I Human chr2 - 113708698 113708696 113708698 TTATTTTTTATTTTTTATTTTTTTTGAGACAGAGTCTCACTCCATTGCCCAGGCTGAAGTGCAGT TTATTTTTTATTTTTTATTTTTTTTGAGACAG__TCTCACTCCATTGCCCAGGCTGAAGTGCAGT ACT A SLC35F5 Ensembl:ENSG00000115084 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs1234664134 Functional Loss DEL dbSNP153 33..34 33 - - - 34271 RMVar_ID_34271 Human_SNP_ID_87647400 A-to-I Human chr2 - 113708714 113708707 113708714 GTAATTATGCAGTATTTTATTTTTTATTTTTTATTTTTTTTGAGACAGAGTCTCACTCCATTGCC GTAATTATGCAGTATTTTATTTTTTATTTTTT_______TTGAGACAGAGTCTCACTCCATTGCC AAAAAAAT A SLC35F5 Ensembl:ENSG00000115084 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs925783358 Functional Loss DEL dbSNP153 33..39 33 - - - Human_RBP_ID_6815683 34272 RMVar_ID_34272 Human_SNP_ID_87647402 A-to-I Human chr2 - 113708714 113708708 113708714 GTAATTATGCAGTATTTTATTTTTTATTTTTTATTTTTTTTGAGACAGAGTCTCACTCCATTGCC GTAATTATGCAGTATTTTATTTTTTATTTTTT______TTTGAGACAGAGTCTCACTCCATTGCC AAAAAAT A SLC35F5 Ensembl:ENSG00000115084 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs937266280 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_6815683 34273 RMVar_ID_34273 Human_SNP_ID_87647404 A-to-I Human chr2 - 113708714 113708713 113708714 GTAATTATGCAGTATTTTATTTTTTATTTTTTATTTTTTTTGAGACAGAGTCTCACTCCATTGCC GTAATTATGCAGTATTTTATTTTTTATTTTTT_TTTTTTTTGAGACAGAGTCTCACTCCATTGCC AT A SLC35F5 Ensembl:ENSG00000115084 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs202130136 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_6815683 34274 RMVar_ID_34274 Human_SNP_ID_87647405 A-to-I Human chr2 - 113708714 113708714 113708714 GTAATTATGCAGTATTTTATTTTTTATTTTTTATTTTTTTTGAGACAGAGTCTCACTCCATTGCC GTAATTATGCAGTATTTTATTTTTTATTTTTTTTTTTTTTTGAGACAGAGTCTCACTCCATTGCC T A SLC35F5 Ensembl:ENSG00000115084 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs182206747 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6815683 34275 RMVar_ID_34275 Human_SNP_ID_87647407 A-to-I Human chr2 - 113708721 113708721 113708721 ATAGCATGTAATTATGCAGTATTTTATTTTTTATTTTTTATTTTTTTTGAGACAGAGTCTCACTC ATAGCATGTAATTATGCAGTATTTTATTTTTTGTTTTTTATTTTTTTTGAGACAGAGTCTCACTC T C SLC35F5 Ensembl:ENSG00000115084 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs766022823 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6815683 34276 RMVar_ID_34276 Human_SNP_ID_87647577 A-to-I Human chr2 - 113709417 113709417 113709417 CCTTCCCTCACTCTTCTCAGCTATAAAGTGAGAAGCGAAATTCAGTATCTTTTAAGATTCCTCTC CCTTCCCTCACTCTTCTCAGCTATAAAGTGAGGAGCGAAATTCAGTATCTTTTAAGATTCCTCTC T C SLC35F5 Ensembl:ENSG00000115084 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs935644 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_3671,GWAS_ID_3672,GWAS_ID_3673,GWAS_ID_3674 34277 RMVar_ID_34277 Human_SNP_ID_87647713 A-to-I Human chr2 - 113709963 113709963 113709963 AAAAACAAAAACAAAAAACAAACAGGCATGGTAGTGCATACCTGTAGTCTGAGCTGCTTGGGAGT AAAAACAAAAACAAAAAACAAACAGGCATGGTGGTGCATACCTGTAGTCTGAGCTGCTTGGGAGT T C SLC35F5 Ensembl:ENSG00000115084 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs551563967 Functional Loss SNV dbSNP153 33..33 33 - - - 34278 RMVar_ID_34278 Human_SNP_ID_87647793 A-to-I Human chr2 - 113710464 113710463 113710464 TGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCATGCCTGGCTAAAACCAATTCTTTAG TGGCCTCCCAAAGTGCTGGGATTACAGGCATG_GCCACCATGCCTGGCTAAAACCAATTCTTTAG CT C SLC35F5 Ensembl:ENSG00000115084 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs781021169 Functional Loss DEL dbSNP153 33..33 33 - - - 34279 RMVar_ID_34279 Human_SNP_ID_87647811 A-to-I Human chr2 - 113710564 113710564 113710564 TTGCTATATTGCCTAATTTTTGTGTTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGC TTGCTATATTGCCTAATTTTTGTGTTTTTAGTGGAGATGGGGTTTCACCATGTTGGCCAGGCTGC T C SLC35F5 Ensembl:ENSG00000115084 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1415089031 Functional Loss SNV dbSNP153 33..33 33 - - - 34280 RMVar_ID_34280 Human_SNP_ID_87647829 A-to-I Human chr2 - 113710664 113710664 113710664 TCAAGCCATCCTCCCACCTCAGTCTCCTGAGTAGTTGGGACTACTGGCATGTGCCCCCATTCCTG TCAAGCCATCCTCCCACCTCAGTCTCCTGAGTCGTTGGGACTACTGGCATGTGCCCCCATTCCTG T G SLC35F5 Ensembl:ENSG00000115084 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1299595341 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13584088 34281 RMVar_ID_34281 Human_SNP_ID_87647834 A-to-I Human chr2 - 113710681 113710681 113710681 ACTGCAACCTCCCAAGCTCAAGCCATCCTCCCACCTCAGTCTCCTGAGTAGTTGGGACTACTGGC ACTGCAACCTCCCAAGCTCAAGCCATCCTCCCGCCTCAGTCTCCTGAGTAGTTGGGACTACTGGC T C SLC35F5 Ensembl:ENSG00000115084 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1381321629 Functional Loss SNV dbSNP153 33..33 33 - - - 34282 RMVar_ID_34282 Human_SNP_ID_87648188 A-to-I Human chr2 - 113712428 113712428 113712428 CCTGTAGTCCCAGCTGCTCGGGAGGCTGAGGCAGCAGAATGGCGTGAACCCGGGAGGCGGAGCCT CCTGTAGTCCCAGCTGCTCGGGAGGCTGAGGCGGCAGAATGGCGTGAACCCGGGAGGCGGAGCCT T C SLC35F5 Ensembl:ENSG00000115084 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1259683099 Functional Loss SNV dbSNP153 33..33 33 - - - 34283 RMVar_ID_34283 Human_SNP_ID_87654280 A-to-I Human chr2 - 113740487 113740487 113740487 TGTAATTTCAAAAAATAATTTTTAAAAACACTATTATCTGCACATACCTTTAAATCTGCTATAAA TGTAATTTCAAAAAATAATTTTTAAAAACACTGTTATCTGCACATACCTTTAAATCTGCTATAAA T C SLC35F5 Ensembl:ENSG00000115084 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1308583148 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13584733 RMVar_hsa_circ_126620,RMVar_hsa_circ_202695,RMVar_hsa_circ_279872,RMVar_hsa_circ_374988,RMVar_hsa_circ_328181,RMVar_hsa_circ_107917,RMVar_hsa_circ_202696,RMVar_hsa_circ_202698,RMVar_hsa_circ_202697,RMVar_hsa_circ_202705,RMVar_hsa_circ_306170,RMVar_hsa_circ_367316,RMVar_hsa_circ_360414,RMVar_hsa_circ_314184,RMVar_hsa_circ_202706,RMVar_hsa_circ_202704,RMVar_hsa_circ_202708,RMVar_hsa_circ_306896,RMVar_hsa_circ_312794,RMVar_hsa_circ_311575,RMVar_hsa_circ_304085,RMVar_hsa_circ_202709,RMVar_hsa_circ_270193,RMVar_hsa_circ_202707,RMVar_hsa_circ_299389,RMVar_hsa_circ_325230,RMVar_hsa_circ_202714,RMVar_hsa_circ_202715,RMVar_hsa_circ_202713,RMVar_hsa_circ_6763,RMVar_hsa_circ_202719,RMVar_hsa_circ_285887,RMVar_hsa_circ_299327,RMVar_hsa_circ_372867,RMVar_hsa_circ_299168,RMVar_hsa_circ_202720,RMVar_hsa_circ_350812,RMVar_hsa_circ_202717,RMVar_hsa_circ_202718,RMVar_hsa_circ_363539,RMVar_hsa_circ_69707,RMVar_hsa_circ_339481,RMVar_hsa_circ_323696,RMVar_hsa_circ_362734,RMVar_hsa_circ_202722 34284 RMVar_ID_34284 Human_SNP_ID_87654290 A-to-I Human chr2 - 113740534 113740534 113740534 TTAACTGTACACTTAAAAATGATCCAAATGGTATATTTTATGTATATTGTAATTTCAAAAAATAA TTAACTGTACACTTAAAAATGATCCAAATGGTGTATTTTATGTATATTGTAATTTCAAAAAATAA T C SLC35F5 Ensembl:ENSG00000115084 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs186232171 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126620,RMVar_hsa_circ_202695,RMVar_hsa_circ_279872,RMVar_hsa_circ_374988,RMVar_hsa_circ_328181,RMVar_hsa_circ_107917,RMVar_hsa_circ_202696,RMVar_hsa_circ_202698,RMVar_hsa_circ_202697,RMVar_hsa_circ_202705,RMVar_hsa_circ_306170,RMVar_hsa_circ_367316,RMVar_hsa_circ_360414,RMVar_hsa_circ_314184,RMVar_hsa_circ_202706,RMVar_hsa_circ_202704,RMVar_hsa_circ_202708,RMVar_hsa_circ_306896,RMVar_hsa_circ_312794,RMVar_hsa_circ_311575,RMVar_hsa_circ_304085,RMVar_hsa_circ_202709,RMVar_hsa_circ_270193,RMVar_hsa_circ_202707,RMVar_hsa_circ_299389,RMVar_hsa_circ_325230,RMVar_hsa_circ_202714,RMVar_hsa_circ_202715,RMVar_hsa_circ_202713,RMVar_hsa_circ_6763,RMVar_hsa_circ_202719,RMVar_hsa_circ_285887,RMVar_hsa_circ_299327,RMVar_hsa_circ_372867,RMVar_hsa_circ_299168,RMVar_hsa_circ_202720,RMVar_hsa_circ_350812,RMVar_hsa_circ_202717,RMVar_hsa_circ_202718,RMVar_hsa_circ_363539,RMVar_hsa_circ_69707,RMVar_hsa_circ_339481,RMVar_hsa_circ_323696,RMVar_hsa_circ_362734,RMVar_hsa_circ_202722 34285 RMVar_ID_34285 Human_SNP_ID_87654295 A-to-I Human chr2 - 113740564 113740546 113740565 TGCATAACAGTGTGAATGTACTTTATGCCATTAACTGTACACTTAAAAATGATCCAAATGGTATA TGCATAACAGTGTGAATGTACTTTATGCCAT___________________GATCCAAATGGTATA CATTTTTAAGTGTACAGTTA C SLC35F5 Ensembl:ENSG00000115084 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1408770984 Functional Loss DEL dbSNP153 32..50 33 - - - RMVar_hsa_circ_126620,RMVar_hsa_circ_202695,RMVar_hsa_circ_279872,RMVar_hsa_circ_374988,RMVar_hsa_circ_328181,RMVar_hsa_circ_107917,RMVar_hsa_circ_202696,RMVar_hsa_circ_202698,RMVar_hsa_circ_202697,RMVar_hsa_circ_202705,RMVar_hsa_circ_306170,RMVar_hsa_circ_367316,RMVar_hsa_circ_360414,RMVar_hsa_circ_314184,RMVar_hsa_circ_202706,RMVar_hsa_circ_202704,RMVar_hsa_circ_202708,RMVar_hsa_circ_306896,RMVar_hsa_circ_312794,RMVar_hsa_circ_311575,RMVar_hsa_circ_304085,RMVar_hsa_circ_202709,RMVar_hsa_circ_270193,RMVar_hsa_circ_202707,RMVar_hsa_circ_299389,RMVar_hsa_circ_325230,RMVar_hsa_circ_202714,RMVar_hsa_circ_202715,RMVar_hsa_circ_202713,RMVar_hsa_circ_6763,RMVar_hsa_circ_202719,RMVar_hsa_circ_285887,RMVar_hsa_circ_299327,RMVar_hsa_circ_372867,RMVar_hsa_circ_299168,RMVar_hsa_circ_202720,RMVar_hsa_circ_350812,RMVar_hsa_circ_202717,RMVar_hsa_circ_202718,RMVar_hsa_circ_363539,RMVar_hsa_circ_69707,RMVar_hsa_circ_339481,RMVar_hsa_circ_323696,RMVar_hsa_circ_362734,RMVar_hsa_circ_202722 34286 RMVar_ID_34286 Human_SNP_ID_87654297 A-to-I Human chr2 - 113740564 113740564 113740564 TGCATAACAGTGTGAATGTACTTTATGCCATTAACTGTACACTTAAAAATGATCCAAATGGTATA TGCATAACAGTGTGAATGTACTTTATGCCATTTACTGTACACTTAAAAATGATCCAAATGGTATA T A SLC35F5 Ensembl:ENSG00000115084 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs989366552 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126620,RMVar_hsa_circ_202695,RMVar_hsa_circ_279872,RMVar_hsa_circ_374988,RMVar_hsa_circ_328181,RMVar_hsa_circ_107917,RMVar_hsa_circ_202696,RMVar_hsa_circ_202698,RMVar_hsa_circ_202697,RMVar_hsa_circ_202705,RMVar_hsa_circ_306170,RMVar_hsa_circ_367316,RMVar_hsa_circ_360414,RMVar_hsa_circ_314184,RMVar_hsa_circ_202706,RMVar_hsa_circ_202704,RMVar_hsa_circ_202708,RMVar_hsa_circ_306896,RMVar_hsa_circ_312794,RMVar_hsa_circ_311575,RMVar_hsa_circ_304085,RMVar_hsa_circ_202709,RMVar_hsa_circ_270193,RMVar_hsa_circ_202707,RMVar_hsa_circ_299389,RMVar_hsa_circ_325230,RMVar_hsa_circ_202714,RMVar_hsa_circ_202715,RMVar_hsa_circ_202713,RMVar_hsa_circ_6763,RMVar_hsa_circ_202719,RMVar_hsa_circ_285887,RMVar_hsa_circ_299327,RMVar_hsa_circ_372867,RMVar_hsa_circ_299168,RMVar_hsa_circ_202720,RMVar_hsa_circ_350812,RMVar_hsa_circ_202717,RMVar_hsa_circ_202718,RMVar_hsa_circ_363539,RMVar_hsa_circ_69707,RMVar_hsa_circ_339481,RMVar_hsa_circ_323696,RMVar_hsa_circ_362734,RMVar_hsa_circ_202722 34287 RMVar_ID_34287 Human_SNP_ID_87656078 A-to-I Human chr2 - 113748220 113748220 113748220 TGAAGGTTACAGTGAGCAGAGACTGAACCACTACACTCCAGTCTGGGTGACAGAGTGAGACTGTC TGAAGGTTACAGTGAGCAGAGACTGAACCACTGCACTCCAGTCTGGGTGACAGAGTGAGACTGTC T C SLC35F5 Ensembl:ENSG00000115084 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs767708903 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569855 RMVar_hsa_circ_126620,RMVar_hsa_circ_202695,RMVar_hsa_circ_279872,RMVar_hsa_circ_328181,RMVar_hsa_circ_107917,RMVar_hsa_circ_202696,RMVar_hsa_circ_202697,RMVar_hsa_circ_306170,RMVar_hsa_circ_360414,RMVar_hsa_circ_202706,RMVar_hsa_circ_27065,RMVar_hsa_circ_202708,RMVar_hsa_circ_312794,RMVar_hsa_circ_304085,RMVar_hsa_circ_270193,RMVar_hsa_circ_202707,RMVar_hsa_circ_202715,RMVar_hsa_circ_6763,RMVar_hsa_circ_372867,RMVar_hsa_circ_299168,RMVar_hsa_circ_350812,RMVar_hsa_circ_202717,RMVar_hsa_circ_202718,RMVar_hsa_circ_69707,RMVar_hsa_circ_339481,RMVar_hsa_circ_362734,RMVar_hsa_circ_28648,RMVar_hsa_circ_202724,RMVar_hsa_circ_122710,RMVar_hsa_circ_343500,RMVar_hsa_circ_302174,RMVar_hsa_circ_202726,RMVar_hsa_circ_202727,RMVar_hsa_circ_202728,RMVar_hsa_circ_375309,RMVar_hsa_circ_317914,RMVar_hsa_circ_202729 34288 RMVar_ID_34288 Human_SNP_ID_87688549 A-to-I Human chr2 - 113880339 113880339 113880339 TCAAGCGATTCTCCTGCCTCAGCCCCCCGAGCAGCTGGTATTACAGGCATATGCCACCCCACCCA TCAAGCGATTCTCCTGCCTCAGCCCCCCGAGCGGCTGGTATTACAGGCATATGCCACCCCACCCA T C ACTR3-AS1,ACTR3-AS1:2,ACTR3-AS1:3,ACTR3-AS1:4,ACTR3-AS1:5,ACTR3-AS1:6,ACTR3-AS1:7,ACTR3-AS1:8,ACTR3-AS1:9,ACTR3-AS1:10,ACTR3-AS1:11,ACTR3-AS1:12,ACTR3-AS1:13 RNACentral:URS0000D56D77,RNACentral:URS0000D577C0,RNACentral:URS000075A0DA,RNACentral:URS0000D576CF,RNACentral:URS0000D5B1C9,RNACentral:URS0000D5C070,RNACentral:URS00009BE5F7,RNACentral:URS0000D5C1B6,RNACentral:URS0000D58D2A,RNACentral:URS0000D56C7D,RNACentral:URS0000D57B2C,RNACentral:URS0000D5B6E1,RNACentral:URS0000D58E3F lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,exon,intron,intron,intron,exon,intron,intron,intron,intron,intron,intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968526553 Functional Loss SNV dbSNP153 33..33 33 - - - 34289 RMVar_ID_34289 Human_SNP_ID_87689022 A-to-I Human chr2 - 113881951 113881951 113881951 AGGATCGCTTGAGCCTGGGAGATTGAGGCCTCAGTGAGCCATGATCATGCCACTGTACTCCAGCC AGGATCGCTTGAGCCTGGGAGATTGAGGCCTCGGTGAGCCATGATCATGCCACTGTACTCCAGCC T C ACTR3-AS1,ACTR3-AS1:2,ACTR3-AS1:3,ACTR3-AS1:4,ACTR3-AS1:5,ACTR3-AS1:6,ACTR3-AS1:7,ACTR3-AS1:8,ACTR3-AS1:9,ACTR3-AS1:10,ACTR3-AS1:11,ACTR3-AS1:12,ACTR3-AS1:13 RNACentral:URS0000D56D77,RNACentral:URS0000D577C0,RNACentral:URS000075A0DA,RNACentral:URS0000D576CF,RNACentral:URS0000D5B1C9,RNACentral:URS0000D5C070,RNACentral:URS00009BE5F7,RNACentral:URS0000D5C1B6,RNACentral:URS0000D58D2A,RNACentral:URS0000D56C7D,RNACentral:URS0000D57B2C,RNACentral:URS0000D5B6E1,RNACentral:URS0000D58E3F lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,intron,exon,exon,exon,exon,intron,exon,exon,exon,exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs898515184 Functional Loss SNV dbSNP153 33..33 33 - - - 34290 RMVar_ID_34290 Human_SNP_ID_87702139 A-to-I Human chr2 + 113933307 113933307 113933307 CTGAGGCAGGTGAATCACAAGGTCAGGAGTTCAAGATCAGCCTGGCTGAGATGGTGAAACCCCGT CTGAGGCAGGTGAATCACAAGGTCAGGAGTTCGAGATCAGCCTGGCTGAGATGGTGAAACCCCGT A G ACTR3 Ensembl:ENSG00000115091 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs796429873 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70362,RMVar_hsa_circ_74295,RMVar_hsa_circ_318996,RMVar_hsa_circ_374683,RMVar_hsa_circ_314045,RMVar_hsa_circ_92558,RMVar_hsa_circ_346175,RMVar_hsa_circ_202737,RMVar_hsa_circ_202738,RMVar_hsa_circ_374871,RMVar_hsa_circ_366237,RMVar_hsa_circ_299555,RMVar_hsa_circ_338230,RMVar_hsa_circ_202739,RMVar_hsa_circ_202741,RMVar_hsa_circ_202742,RMVar_hsa_circ_202740,RMVar_hsa_circ_306467,RMVar_hsa_circ_355565,RMVar_hsa_circ_85228,RMVar_hsa_circ_202745,RMVar_hsa_circ_202746,RMVar_hsa_circ_202747,RMVar_hsa_circ_298356,RMVar_hsa_circ_311521,RMVar_hsa_circ_118540 34291 RMVar_ID_34291 Human_SNP_ID_87702298 A-to-I Human chr2 + 113933819 113933819 113933819 CTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCGCCCGCCACCGCACCTGGCTAAGTTTT CTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTGCAGGCGCCCGCCACCGCACCTGGCTAAGTTTT A G ACTR3 Ensembl:ENSG00000115091 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270958654 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70362,RMVar_hsa_circ_74295,RMVar_hsa_circ_318996,RMVar_hsa_circ_374683,RMVar_hsa_circ_314045,RMVar_hsa_circ_92558,RMVar_hsa_circ_346175,RMVar_hsa_circ_202737,RMVar_hsa_circ_202738,RMVar_hsa_circ_374871,RMVar_hsa_circ_366237,RMVar_hsa_circ_299555,RMVar_hsa_circ_338230,RMVar_hsa_circ_202739,RMVar_hsa_circ_202741,RMVar_hsa_circ_202742,RMVar_hsa_circ_202740,RMVar_hsa_circ_306467,RMVar_hsa_circ_355565,RMVar_hsa_circ_85228,RMVar_hsa_circ_202745,RMVar_hsa_circ_202746,RMVar_hsa_circ_202747,RMVar_hsa_circ_298356,RMVar_hsa_circ_311521,RMVar_hsa_circ_118540 34292 RMVar_ID_34292 Human_SNP_ID_87706138 A-to-I Human chr2 + 113949120 113949120 113949120 TGGAAAAAGGCAGGGCGTGGTGGCTCACACCTATAATCCCAGCACTTTGGGAGGCTGAGGCAGGC TGGAAAAAGGCAGGGCGTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGC A G ACTR3 Ensembl:ENSG00000115091 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1052955759 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8870 RMVar_hsa_circ_70362,RMVar_hsa_circ_74295,RMVar_hsa_circ_374683,RMVar_hsa_circ_346175,RMVar_hsa_circ_202738,RMVar_hsa_circ_374871,RMVar_hsa_circ_202739,RMVar_hsa_circ_85228,RMVar_hsa_circ_202746,RMVar_hsa_circ_298356,RMVar_hsa_circ_346894,RMVar_hsa_circ_202749,RMVar_hsa_circ_202752,RMVar_hsa_circ_290361,RMVar_hsa_circ_275270,RMVar_hsa_circ_202751 34293 RMVar_ID_34293 Human_SNP_ID_87706313 A-to-I Human chr2 + 113949655 113949655 113949655 GTGATCATAACTCAGTGTAACCTCGAATTCCTAGGGTCAAGCAATCCTTTTTCCTCAGCCCTCTC GTGATCATAACTCAGTGTAACCTCGAATTCCTGGGGTCAAGCAATCCTTTTTCCTCAGCCCTCTC A G ACTR3 Ensembl:ENSG00000115091 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs999736785 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70362,RMVar_hsa_circ_74295,RMVar_hsa_circ_374683,RMVar_hsa_circ_346175,RMVar_hsa_circ_202738,RMVar_hsa_circ_374871,RMVar_hsa_circ_202739,RMVar_hsa_circ_85228,RMVar_hsa_circ_202746,RMVar_hsa_circ_298356,RMVar_hsa_circ_346894,RMVar_hsa_circ_202749,RMVar_hsa_circ_202752,RMVar_hsa_circ_290361,RMVar_hsa_circ_275270,RMVar_hsa_circ_202751 34294 RMVar_ID_34294 Human_SNP_ID_87706316 A-to-I Human chr2 + 113949665 113949665 113949665 CTCAGTGTAACCTCGAATTCCTAGGGTCAAGCAATCCTTTTTCCTCAGCCCTCTCAAGTAGCTGG CTCAGTGTAACCTCGAATTCCTAGGGTCAAGCCATCCTTTTTCCTCAGCCCTCTCAAGTAGCTGG A C ACTR3 Ensembl:ENSG00000115091 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1298707252 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569857 RMVar_hsa_circ_70362,RMVar_hsa_circ_74295,RMVar_hsa_circ_374683,RMVar_hsa_circ_346175,RMVar_hsa_circ_202738,RMVar_hsa_circ_374871,RMVar_hsa_circ_202739,RMVar_hsa_circ_85228,RMVar_hsa_circ_202746,RMVar_hsa_circ_298356,RMVar_hsa_circ_346894,RMVar_hsa_circ_202749,RMVar_hsa_circ_202752,RMVar_hsa_circ_290361,RMVar_hsa_circ_275270,RMVar_hsa_circ_202751 34295 RMVar_ID_34295 Human_SNP_ID_87706324 A-to-I Human chr2 + 113949728 113949728 113949728 GGAACTACAGGTGTGTGCCACCATGCCTAGCTAGTTTTTAAATTTTTTGTAGAGACAGGGTCTCG GGAACTACAGGTGTGTGCCACCATGCCTAGCTGGTTTTTAAATTTTTTGTAGAGACAGGGTCTCG A G ACTR3 Ensembl:ENSG00000115091 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs866331194 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70362,RMVar_hsa_circ_74295,RMVar_hsa_circ_374683,RMVar_hsa_circ_346175,RMVar_hsa_circ_202738,RMVar_hsa_circ_374871,RMVar_hsa_circ_202739,RMVar_hsa_circ_85228,RMVar_hsa_circ_202746,RMVar_hsa_circ_298356,RMVar_hsa_circ_346894,RMVar_hsa_circ_202749,RMVar_hsa_circ_202752,RMVar_hsa_circ_290361,RMVar_hsa_circ_275270,RMVar_hsa_circ_202751 34296 RMVar_ID_34296 Human_SNP_ID_87834889 A-to-I Human chr2 + 114469607 114469607 114469607 AAAATTAGCTGGGAGTGGTGGTGCATGCCTGTAATCCTAGCTAGTCAGGAGGCTGAGGCAGGAGA AAAATTAGCTGGGAGTGGTGGTGCATGCCTGTGATCCTAGCTAGTCAGGAGGCTGAGGCAGGAGA A G DPP10 Ensembl:ENSG00000175497 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1445108317 Functional Loss SNV dbSNP153 33..33 33 - - - 34297 RMVar_ID_34297 Human_SNP_ID_87836692 A-to-I Human chr2 + 114477180 114477180 114477180 ATGGTTTCACCATGTTGGACAGGCAGGTCTTGAACTCCTGACCTCAAATGATCCAAGGCCAAGGA ATGGTTTCACCATGTTGGACAGGCAGGTCTTGCACTCCTGACCTCAAATGATCCAAGGCCAAGGA A C DPP10 Ensembl:ENSG00000175497 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs914980904 Functional Loss SNV dbSNP153 33..33 33 - - - 34298 RMVar_ID_34298 Human_SNP_ID_87855668 A-to-I Human chr2 + 114549451 114549451 114549451 TTGGGATGCCAAGGTGGGCAGATCACGTGGTCAGGAGTTCAAGACCAGCCTGGCCAACATTGGGA TTGGGATGCCAAGGTGGGCAGATCACGTGGTCGGGAGTTCAAGACCAGCCTGGCCAACATTGGGA A G DPP10 Ensembl:ENSG00000175497 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1288895988 Functional Loss SNV dbSNP153 33..33 33 - - - 34299 RMVar_ID_34299 Human_SNP_ID_87922403 A-to-I Human chr2 + 114820834 114820834 114820834 CTGGCGATGAGATTTGGGTGGGTGCACAGCCAAACCATATCATTCTTCCCCTGGACCCTCCCAAA CTGGCGATGAGATTTGGGTGGGTGCACAGCCATACCATATCATTCTTCCCCTGGACCCTCCCAAA A T DPP10 Ensembl:ENSG00000175497 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1341491355 Functional Loss SNV dbSNP153 33..33 33 - - - 34300 RMVar_ID_34300 Human_SNP_ID_87927503 A-to-I Human chr2 + 114838478 114838478 114838478 AGGATTACAGCTGTGAGCTACCACGCCTAGCTAATTTTTTTGGATTTTTAGTAGAGATGGGATTT AGGATTACAGCTGTGAGCTACCACGCCTAGCTGATTTTTTTGGATTTTTAGTAGAGATGGGATTT A G DPP10 Ensembl:ENSG00000175497 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1364400927 Functional Loss SNV dbSNP153 33..33 33 - - - 34301 RMVar_ID_34301 Human_SNP_ID_87935543 A-to-I Human chr2 + 114871823 114871823 114871823 AGTGGTGAACAAGCGAGCAAACTTTCATCTGTATTTATAGCCACTCCCCATCACTTGCATTACTG AGTGGTGAACAAGCGAGCAAACTTTCATCTGTGTTTATAGCCACTCCCCATCACTTGCATTACTG A G DPP10 Ensembl:ENSG00000175497 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs577817791 Functional Loss SNV dbSNP153 33..33 33 - - - 34302 RMVar_ID_34302 Human_SNP_ID_87938771 A-to-I Human chr2 + 114884615 114884615 114884615 TCGAGGAACAGGTGGTGTTTGGTTATATGAATATGTTCTTTAATGGTGATTTCTGAGATTTTGGT TCGAGGAACAGGTGGTGTTTGGTTATATGAATGTGTTCTTTAATGGTGATTTCTGAGATTTTGGT A G DPP10 Ensembl:ENSG00000175497 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1044196630 Functional Loss SNV dbSNP153 33..33 33 - - - 34303 RMVar_ID_34303 Human_SNP_ID_88013001 A-to-I Human chr2 + 115178421 115178421 115178421 AACCACAGTTTCCTCATCTTTAAAATGAGAACAACAAACTAACTTGCACACAGTGTTCTAATGAG AACCACAGTTTCCTCATCTTTAAAATGAGAACCACAAACTAACTTGCACACAGTGTTCTAATGAG A C DPP10 Ensembl:ENSG00000175497 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs538452884 Functional Loss SNV dbSNP153 33..33 33 - - - 34304 RMVar_ID_34304 Human_SNP_ID_88755336 A-to-I Human chr2 - 117993207 117993207 117993207 TTTTTTTAGTAGAGATGGGGTTTCACCGTGTTAGCCAGGATGGTCTCGATCTCCTGACCTCGAGG TTTTTTTAGTAGAGATGGGGTTTCACCGTGTTCGCCAGGATGGTCTCGATCTCCTGACCTCGAGG T G CCDC93 Ensembl:ENSG00000125633 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459368534 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119248,RMVar_hsa_circ_82738,RMVar_hsa_circ_202803,RMVar_hsa_circ_202804,RMVar_hsa_circ_97897,RMVar_hsa_circ_305022,RMVar_hsa_circ_202812,RMVar_hsa_circ_366341 34305 RMVar_ID_34305 Human_SNP_ID_88783200 A-to-I Human chr2 - 118109730 118109730 118109730 AAAACATAAAAGCAGATTAAAGTTTGGCATACAAGATCTCAGTCTGATAGTAATTGCTTTAAAAC AAAACATAAAAGCAGATTAAAGTTTGGCATACGAGATCTCAGTCTGATAGTAATTGCTTTAAAAC T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1272258416 Functional Loss SNV dbSNP153 33..33 33 - - - 34306 RMVar_ID_34306 Human_SNP_ID_89181261 A-to-I Human chr2 + 119717325 119717325 119717325 GCCCTCCAGCCTGGGCAACAGAGTATGACTCCATCTGGAAAAAAAAAAAAGAAAAAGAAAAAAAA GCCCTCCAGCCTGGGCAACAGAGTATGACTCCGTCTGGAAAAAAAAAAAAGAAAAAGAAAAAAAA A G lnc-TMEM177-3,lnc-TMEM177-3:2 RNACentral:URS00008BF2EF,RNACentral:URS00009B1595 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1252083476 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67850,RMVar_hsa_circ_85507,RMVar_hsa_circ_202832 34307 RMVar_ID_34307 Human_SNP_ID_89238756 A-to-I Human chr2 + 119966352 119966352 119966352 ATGATCACAGCTCACTGTAACCTCTGCCTCCCAGGCTCAAGTGATCCTCCTGCCTCAGCCCCCGG ATGATCACAGCTCACTGTAACCTCTGCCTCCCGGGCTCAAGTGATCCTCCTGCCTCAGCCCCCGG A G PTPN4 Ensembl:ENSG00000088179 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1254905834 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85170,RMVar_hsa_circ_202843,RMVar_hsa_circ_363595,RMVar_hsa_circ_302893,RMVar_hsa_circ_202870,RMVar_hsa_circ_346078,RMVar_hsa_circ_202871,RMVar_hsa_circ_291878,RMVar_hsa_circ_202878,RMVar_hsa_circ_97385,RMVar_hsa_circ_297521,RMVar_hsa_circ_202879,RMVar_hsa_circ_332801,RMVar_hsa_circ_202892,RMVar_hsa_circ_202893,RMVar_hsa_circ_373613,RMVar_hsa_circ_202897,RMVar_hsa_circ_202894,RMVar_hsa_circ_286186,RMVar_hsa_circ_286012,RMVar_hsa_circ_202900,RMVar_hsa_circ_305548,RMVar_hsa_circ_365396,RMVar_hsa_circ_202901,RMVar_hsa_circ_322854,RMVar_hsa_circ_202904,RMVar_hsa_circ_202902,RMVar_hsa_circ_278999 34308 RMVar_ID_34308 Human_SNP_ID_197377926 A-to-I Human chr4 + 105020251 105020251 105020251 CCTGTAGTCCCGGCTGCTTGGGAGGCTGAGGCAGGAGAATGGTGTGAACCCGGGAGGCGGAGCTT CCTGTAGTCCCGGCTGCTTGGGAGGCTGAGGCGGGAGAATGGTGTGAACCCGGGAGGCGGAGCTT A G AC096577.1 Ensembl:ENSG00000248373 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037808827 Functional Loss SNV dbSNP153 33..33 33 - - - 34309 RMVar_ID_34309 Human_SNP_ID_197435687 A-to-I Human chr4 + 105259176 105259176 105259176 GGGAGGCTGAGGCGGGAAGATCACTTGAGCCCAGAAGTTCAGGTTCAACCTGAGCAACATAGCAA GGGAGGCTGAGGCGGGAAGATCACTTGAGCCCGGAAGTTCAGGTTCAACCTGAGCAACATAGCAA A G TET2 Ensembl:ENSG00000168769 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1051912807 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_53127,RMVar_hsa_circ_82348,RMVar_hsa_circ_227783 34310 RMVar_ID_34310 Human_SNP_ID_197472403 A-to-I Human chr4 - 105403317 105403317 105403317 TGATAGGCTGGGCATGGTGGCTCACACTTGTAATCCCAACACTTTGGGAGGCCAAGGCAGGAGGA TGATAGGCTGGGCATGGTGGCTCACACTTGTACTCCCAACACTTTGGGAGGCCAAGGCAGGAGGA T G PPA2 Ensembl:ENSG00000138777 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1434890096 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_227793,RMVar_hsa_circ_227789,RMVar_hsa_circ_332990,RMVar_hsa_circ_280822,RMVar_hsa_circ_304059,RMVar_hsa_circ_330943,RMVar_hsa_circ_302559,RMVar_hsa_circ_227797,RMVar_hsa_circ_285486,RMVar_hsa_circ_227791,RMVar_hsa_circ_227792,RMVar_hsa_circ_332629,RMVar_hsa_circ_367914,RMVar_hsa_circ_296894,RMVar_hsa_circ_301626,RMVar_hsa_circ_296636,RMVar_hsa_circ_227799,RMVar_hsa_circ_227800,RMVar_hsa_circ_227798,RMVar_hsa_circ_227796,RMVar_hsa_circ_364052 34311 RMVar_ID_34311 Human_SNP_ID_197476774 A-to-I Human chr4 - 105421795 105421795 105421795 AAAGGGATCTACCCGCCTCAGCCTCCCAAAGTACTGGGATTACAGGTTTGAGCCACCATGCCCAG AAAGGGATCTACCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTTTGAGCCACCATGCCCAG T C PPA2 Ensembl:ENSG00000138777 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1313188667 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25830917 RMVar_hsa_circ_227793,RMVar_hsa_circ_227789,RMVar_hsa_circ_332990,RMVar_hsa_circ_280822,RMVar_hsa_circ_304059,RMVar_hsa_circ_330943,RMVar_hsa_circ_302559,RMVar_hsa_circ_227797,RMVar_hsa_circ_285486,RMVar_hsa_circ_227791,RMVar_hsa_circ_227792,RMVar_hsa_circ_332629,RMVar_hsa_circ_367914,RMVar_hsa_circ_296894,RMVar_hsa_circ_301626,RMVar_hsa_circ_296636,RMVar_hsa_circ_227799,RMVar_hsa_circ_227800,RMVar_hsa_circ_227798,RMVar_hsa_circ_227796,RMVar_hsa_circ_364052 34312 RMVar_ID_34312 Human_SNP_ID_197476775 A-to-I Human chr4 - 105421795 105421795 105421795 AAAGGGATCTACCCGCCTCAGCCTCCCAAAGTACTGGGATTACAGGTTTGAGCCACCATGCCCAG AAAGGGATCTACCCGCCTCAGCCTCCCAAAGTCCTGGGATTACAGGTTTGAGCCACCATGCCCAG T G PPA2 Ensembl:ENSG00000138777 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1313188667 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25830917 RMVar_hsa_circ_227793,RMVar_hsa_circ_227789,RMVar_hsa_circ_332990,RMVar_hsa_circ_280822,RMVar_hsa_circ_304059,RMVar_hsa_circ_330943,RMVar_hsa_circ_302559,RMVar_hsa_circ_227797,RMVar_hsa_circ_285486,RMVar_hsa_circ_227791,RMVar_hsa_circ_227792,RMVar_hsa_circ_332629,RMVar_hsa_circ_367914,RMVar_hsa_circ_296894,RMVar_hsa_circ_301626,RMVar_hsa_circ_296636,RMVar_hsa_circ_227799,RMVar_hsa_circ_227800,RMVar_hsa_circ_227798,RMVar_hsa_circ_227796,RMVar_hsa_circ_364052 34313 RMVar_ID_34313 Human_SNP_ID_197480506 A-to-I Human chr4 - 105438028 105438028 105438028 TTTTTTTTAAAAAAAAAATTTTAGACTTGGGAAGATCCCCATGAAAAAGATAAGAGCACGAACTG TTTTTTTTAAAAAAAAAATTTTAGACTTGGGAGGATCCCCATGAAAAAGATAAGAGCACGAACTG T C PPA2 Ensembl:ENSG00000138777 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs962824637 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8581799,Human_RBP_ID_22457732,Human_RBP_ID_25774696,Human_RBP_ID_26688326 Human_Splice_Rec_588980,Human_Splice_Rec_588981,Human_Splice_Rec_589024,Human_Splice_Rec_589025,Human_Splice_Rec_589080,Human_Splice_Rec_589081,Human_Splice_Rec_589108,Human_Splice_Rec_589109,Human_Splice_Rec_589124,Human_Splice_Rec_589125,Human_Splice_Rec_589138,Human_Splice_Rec_589139,Human_Splice_Rec_589158,Human_Splice_Rec_589159,Human_Splice_Rec_589172,Human_Splice_Rec_589173,Human_Splice_Rec_589186,Human_Splice_Rec_589187,Human_Splice_Rec_589200,Human_Splice_Rec_589201,Human_Splice_Rec_589212,Human_Splice_Rec_589222 RMVar_hsa_circ_332990,RMVar_hsa_circ_280822,RMVar_hsa_circ_304059,RMVar_hsa_circ_302559,RMVar_hsa_circ_17332,RMVar_hsa_circ_227797,RMVar_hsa_circ_227791,RMVar_hsa_circ_227792,RMVar_hsa_circ_332629,RMVar_hsa_circ_367914,RMVar_hsa_circ_296894,RMVar_hsa_circ_301626,RMVar_hsa_circ_296636,RMVar_hsa_circ_227799,RMVar_hsa_circ_227800,RMVar_hsa_circ_227798,RMVar_hsa_circ_227804,RMVar_hsa_circ_285595,RMVar_hsa_circ_288978,RMVar_hsa_circ_293852,RMVar_hsa_circ_364052,RMVar_hsa_circ_288106,RMVar_hsa_circ_270444,RMVar_hsa_circ_227805,RMVar_hsa_circ_227802,RMVar_hsa_circ_227803,RMVar_hsa_circ_335661,RMVar_hsa_circ_227801,RMVar_hsa_circ_369360,RMVar_hsa_circ_309711,RMVar_hsa_circ_227806,RMVar_hsa_circ_227807 34314 RMVar_ID_34314 Human_SNP_ID_197578899 A-to-I Human chr4 + 105846161 105846161 105846161 TATATTTCTGCCAGGCATGGTGGCTCATGCCTATAATCCCAGCACTTTGAGAGGCCAAGGTGGGA TATATTTCTGCCAGGCATGGTGGCTCATGCCTGTAATCCCAGCACTTTGAGAGGCCAAGGTGGGA A G GSTCD Ensembl:ENSG00000138780 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs992470704 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8212055,Human_RBP_ID_26518141 34315 RMVar_ID_34315 Human_SNP_ID_197579070 A-to-I Human chr4 + 105846893 105846893 105846893 GTTGGCCAGGCTGGTTTCGAACTCCTGACCTCAGGTGATCTACCCGCCTCAGCCTCCCAAAGTGC GTTGGCCAGGCTGGTTTCGAACTCCTGACCTCGGGTGATCTACCCGCCTCAGCCTCCCAAAGTGC A G GSTCD Ensembl:ENSG00000138780 Protein coding 3'UTR GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs753779963 Functional Loss SNV dbSNP153 33..33 33 - - - 34316 RMVar_ID_34316 Human_SNP_ID_197579444 A-to-I Human chr4 + 105848607 105848607 105848607 GAACAAAAATAGAATGGGGAGCCGGGCGTGGTAGCTCACGCCTGTAATCTCAGCACTTTGGGATG GAACAAAAATAGAATGGGGAGCCGGGCGTGGTGGCTCACGCCTGTAATCTCAGCACTTTGGGATG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1228576537 Functional Loss SNV dbSNP153 33..33 33 - - - 34317 RMVar_ID_34317 Human_SNP_ID_197584149 A-to-I Human chr4 - 105867463 105867463 105867463 CTCTAACCTCAGCCTCCCAAGTAGTTGGCTCTACAGGTGTGTGCCACCATAGCTGGCTAATTTAT CTCTAACCTCAGCCTCCCAAGTAGTTGGCTCTGCAGGTGTGTGCCACCATAGCTGGCTAATTTAT T C INTS12 Ensembl:ENSG00000138785 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1233930538 Functional Loss SNV dbSNP153 33..33 33 - - - 34318 RMVar_ID_34318 Human_SNP_ID_197584154 A-to-I Human chr4 - 105867476 105867476 105867476 GGCTTAAGCAATCCTCTAACCTCAGCCTCCCAAGTAGTTGGCTCTACAGGTGTGTGCCACCATAG GGCTTAAGCAATCCTCTAACCTCAGCCTCCCAGGTAGTTGGCTCTACAGGTGTGTGCCACCATAG T C INTS12 Ensembl:ENSG00000138785 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1366114739 Functional Loss SNV dbSNP153 33..33 33 - - - 34319 RMVar_ID_34319 Human_SNP_ID_197669471 A-to-I Human chr4 - 106228904 106228904 106228904 AATGGCTTTTACCCAAAAGATAGGCAATAACAAATGCTGGTGAGGATGTAGAGAAAAAGGAACCC AATGGCTTTTACCCAAAAGATAGGCAATAACAGATGCTGGTGAGGATGTAGAGAAAAAGGAACCC T C TBCK Ensembl:ENSG00000145348 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs770199583 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1328,RMVar_hsa_circ_227835,RMVar_hsa_circ_321555,RMVar_hsa_circ_90978,RMVar_hsa_circ_356553,RMVar_hsa_circ_227834,RMVar_hsa_circ_338907,RMVar_hsa_circ_323564,RMVar_hsa_circ_306371,RMVar_hsa_circ_71717,RMVar_hsa_circ_304302,RMVar_hsa_circ_72247,RMVar_hsa_circ_34363,RMVar_hsa_circ_34556,RMVar_hsa_circ_33653,RMVar_hsa_circ_298855,RMVar_hsa_circ_32567,RMVar_hsa_circ_276277,RMVar_hsa_circ_227842,RMVar_hsa_circ_328772,RMVar_hsa_circ_332745,RMVar_hsa_circ_334498,RMVar_hsa_circ_365281,RMVar_hsa_circ_333706,RMVar_hsa_circ_331382,RMVar_hsa_circ_312346,RMVar_hsa_circ_280616,RMVar_hsa_circ_288044,RMVar_hsa_circ_62763,RMVar_hsa_circ_41659,RMVar_hsa_circ_227846,RMVar_hsa_circ_227848,RMVar_hsa_circ_227849,RMVar_hsa_circ_227847,RMVar_hsa_circ_340220,RMVar_hsa_circ_227844,RMVar_hsa_circ_227845,RMVar_hsa_circ_227843,RMVar_hsa_circ_311638,RMVar_hsa_circ_317562,RMVar_hsa_circ_65815,RMVar_hsa_circ_77832,RMVar_hsa_circ_24574,RMVar_hsa_circ_3665,RMVar_hsa_circ_115708,RMVar_hsa_circ_227853,RMVar_hsa_circ_227855,RMVar_hsa_circ_227854,RMVar_hsa_circ_317948,RMVar_hsa_circ_227852,RMVar_hsa_circ_349378,RMVar_hsa_circ_331451,RMVar_hsa_circ_281750,RMVar_hsa_circ_311695,RMVar_hsa_circ_25907,RMVar_hsa_circ_26416,RMVar_hsa_circ_9982,RMVar_hsa_circ_227861,RMVar_hsa_circ_227863,RMVar_hsa_circ_227864,RMVar_hsa_circ_227865,RMVar_hsa_circ_227862 34320 RMVar_ID_34320 Human_SNP_ID_197669502 A-to-I Human chr4 - 106229068 106229068 106229068 AAATCTAATAATCTGATTTTAAAAAGGGCAAAAGATTTGATTACACATTTCTCAAAAGAAGACAT AAATCTAATAATCTGATTTTAAAAAGGGCAAACGATTTGATTACACATTTCTCAAAAGAAGACAT T G TBCK Ensembl:ENSG00000145348 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1050332982 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1328,RMVar_hsa_circ_227835,RMVar_hsa_circ_321555,RMVar_hsa_circ_90978,RMVar_hsa_circ_356553,RMVar_hsa_circ_227834,RMVar_hsa_circ_338907,RMVar_hsa_circ_323564,RMVar_hsa_circ_306371,RMVar_hsa_circ_71717,RMVar_hsa_circ_304302,RMVar_hsa_circ_72247,RMVar_hsa_circ_34363,RMVar_hsa_circ_34556,RMVar_hsa_circ_33653,RMVar_hsa_circ_298855,RMVar_hsa_circ_32567,RMVar_hsa_circ_276277,RMVar_hsa_circ_227842,RMVar_hsa_circ_328772,RMVar_hsa_circ_332745,RMVar_hsa_circ_334498,RMVar_hsa_circ_365281,RMVar_hsa_circ_333706,RMVar_hsa_circ_331382,RMVar_hsa_circ_312346,RMVar_hsa_circ_280616,RMVar_hsa_circ_288044,RMVar_hsa_circ_62763,RMVar_hsa_circ_41659,RMVar_hsa_circ_227846,RMVar_hsa_circ_227848,RMVar_hsa_circ_227849,RMVar_hsa_circ_227847,RMVar_hsa_circ_340220,RMVar_hsa_circ_227844,RMVar_hsa_circ_227845,RMVar_hsa_circ_227843,RMVar_hsa_circ_311638,RMVar_hsa_circ_317562,RMVar_hsa_circ_65815,RMVar_hsa_circ_77832,RMVar_hsa_circ_24574,RMVar_hsa_circ_3665,RMVar_hsa_circ_115708,RMVar_hsa_circ_227853,RMVar_hsa_circ_227855,RMVar_hsa_circ_227854,RMVar_hsa_circ_317948,RMVar_hsa_circ_227852,RMVar_hsa_circ_349378,RMVar_hsa_circ_331451,RMVar_hsa_circ_281750,RMVar_hsa_circ_311695,RMVar_hsa_circ_25907,RMVar_hsa_circ_26416,RMVar_hsa_circ_9982,RMVar_hsa_circ_227861,RMVar_hsa_circ_227863,RMVar_hsa_circ_227864,RMVar_hsa_circ_227865,RMVar_hsa_circ_227862 34321 RMVar_ID_34321 Human_SNP_ID_197673498 A-to-I Human chr4 - 106245531 106245531 106245531 CCACCCCTTAAGGGCAAGGAAACACTTTGTCTAGAGTGACTGGCTCACTTAAAGATTGAGACCTA CCACCCCTTAAGGGCAAGGAAACACTTTGTCTGGAGTGACTGGCTCACTTAAAGATTGAGACCTA T C TBCK Ensembl:ENSG00000145348 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs964843495 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1328,RMVar_hsa_circ_227835,RMVar_hsa_circ_90978,RMVar_hsa_circ_356553,RMVar_hsa_circ_227834,RMVar_hsa_circ_71717,RMVar_hsa_circ_304302,RMVar_hsa_circ_34363,RMVar_hsa_circ_298855,RMVar_hsa_circ_276277,RMVar_hsa_circ_227842,RMVar_hsa_circ_332745,RMVar_hsa_circ_365281,RMVar_hsa_circ_331382,RMVar_hsa_circ_280616,RMVar_hsa_circ_340220,RMVar_hsa_circ_227844,RMVar_hsa_circ_227845,RMVar_hsa_circ_227843,RMVar_hsa_circ_77832,RMVar_hsa_circ_317948,RMVar_hsa_circ_227852,RMVar_hsa_circ_331451,RMVar_hsa_circ_281750,RMVar_hsa_circ_26416,RMVar_hsa_circ_227863,RMVar_hsa_circ_227864,RMVar_hsa_circ_227865,RMVar_hsa_circ_377286,RMVar_hsa_circ_353933,RMVar_hsa_circ_11453,RMVar_hsa_circ_227873,RMVar_hsa_circ_227869,RMVar_hsa_circ_265377,RMVar_hsa_circ_319829,RMVar_hsa_circ_375389,RMVar_hsa_circ_366196,RMVar_hsa_circ_315268,RMVar_hsa_circ_227874,RMVar_hsa_circ_227875,RMVar_hsa_circ_70166,RMVar_hsa_circ_346162,RMVar_hsa_circ_348240,RMVar_hsa_circ_227876 34322 RMVar_ID_34322 Human_SNP_ID_198051994 A-to-I Human chr4 - 107822465 107822465 107822465 TATTTTTAGCAGAGACAGGGTCTCAACATGTTAGTCAGGCTGTTCTCGAACTCTTGACCTTGCGA TATTTTTAGCAGAGACAGGGTCTCAACATGTTGGTCAGGCTGTTCTCGAACTCTTGACCTTGCGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1011144065 Functional Loss SNV dbSNP153 33..33 33 - - - 34323 RMVar_ID_34323 Human_SNP_ID_198097586 A-to-I Human chr4 + 108023690 108023690 108023690 GAAGGAGCATTGTATACTGCAAGCTTGTCCACATGCTGTAAAGAGCAATCCGTGCCTCCTGTTCT GAAGGAGCATTGTATACTGCAAGCTTGTCCACGTGCTGTAAAGAGCAATCCGTGCCTCCTGTTCT A G HADH Ensembl:ENSG00000138796 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4956034 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_3675,GWAS_ID_3676 RMVar_hsa_circ_15615,RMVar_hsa_circ_320066,RMVar_hsa_circ_329457,RMVar_hsa_circ_345064,RMVar_hsa_circ_26815,RMVar_hsa_circ_227914,RMVar_hsa_circ_227913,RMVar_hsa_circ_33012 34324 RMVar_ID_34324 Human_SNP_ID_198098043 A-to-I Human chr4 + 108025698 108025698 108025698 ATCACTTGAGCCCAGGAGTTCGAGACCAGCCTAGGCAACATGGCAAAAACCCTCTCTACAGAAAA ATCACTTGAGCCCAGGAGTTCGAGACCAGCCTGGGCAACATGGCAAAAACCCTCTCTACAGAAAA A G HADH Ensembl:ENSG00000138796 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs571779007 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15615,RMVar_hsa_circ_320066,RMVar_hsa_circ_329457,RMVar_hsa_circ_345064,RMVar_hsa_circ_26815,RMVar_hsa_circ_227914,RMVar_hsa_circ_227913,RMVar_hsa_circ_33012 34325 RMVar_ID_34325 Human_SNP_ID_198103927 A-to-I Human chr4 - 108050365 108050365 108050365 CCATTCTCAAGCAGGGCTAACACCTCCAATCTAGAGCACCCTGCACTTCCGGCTCCACCAGTCTT CCATTCTCAAGCAGGGCTAACACCTCCAATCTGGAGCACCCTGCACTTCCGGCTCCACCAGTCTT T C LEF1 Ensembl:ENSG00000138795 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1560750269 Functional Loss SNV dbSNP153 33..33 33 - - - 34326 RMVar_ID_34326 Human_SNP_ID_198103937 A-to-I Human chr4 - 108050425 108050425 108050425 CTGGCACAGCGAACTGTGAAGTACTGAGGTACAGACAACTTCCATGGCCCTGCTGTGGCCCCATT CTGGCACAGCGAACTGTGAAGTACTGAGGTACGGACAACTTCCATGGCCCTGCTGTGGCCCCATT T C LEF1 Ensembl:ENSG00000138795 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs980925350 Functional Loss SNV dbSNP153 33..33 33 - - - 34327 RMVar_ID_34327 Human_SNP_ID_198240644 A-to-I Human chr4 + 108623039 108623039 108623039 GTTGCAGGAGATGATGGACAACAAAGGTAGAAAAGCCAGATTATGGCCAGGTGTGGTGGCTTATG GTTGCAGGAGATGATGGACAACAAAGGTAGAACAGCCAGATTATGGCCAGGTGTGGTGGCTTATG A C RPL34 Ensembl:ENSG00000109475 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs890415965 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_356074 34328 RMVar_ID_34328 Human_SNP_ID_198240654 A-to-I Human chr4 + 108623069 108623069 108623069 AAAAGCCAGATTATGGCCAGGTGTGGTGGCTTATGCCTGAAATCCCAACACTTTGGGAGGCGGAG AAAAGCCAGATTATGGCCAGGTGTGGTGGCTTGTGCCTGAAATCCCAACACTTTGGGAGGCGGAG A G RPL34 Ensembl:ENSG00000109475 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs561310770 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17574834 RMVar_hsa_circ_356074 34329 RMVar_ID_34329 Human_SNP_ID_198240695 A-to-I Human chr4 + 108623222 108623222 108623222 GGGCGTGGTGGCGCATGCCTGTGATCCCAGCTACTCAGAGACTGAGGCAGGAGAATTGCTGGAAG GGGCGTGGTGGCGCATGCCTGTGATCCCAGCTTCTCAGAGACTGAGGCAGGAGAATTGCTGGAAG A T RPL34 Ensembl:ENSG00000109475 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs926586462 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_356074 34330 RMVar_ID_34330 Human_SNP_ID_198240703 A-to-I Human chr4 + 108623252 108623252 108623252 CTACTCAGAGACTGAGGCAGGAGAATTGCTGGAAGCTGGGAGGCAGAGGTTGTGGTGAGCTGCGA CTACTCAGAGACTGAGGCAGGAGAATTGCTGGGAGCTGGGAGGCAGAGGTTGTGGTGAGCTGCGA A G RPL34 Ensembl:ENSG00000109475 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs929509532 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_356074 34331 RMVar_ID_34331 Human_SNP_ID_198240801 A-to-I Human chr4 + 108623567 108623567 108623567 GAATAGCTGGGACTGCAGGCACATGCCACCACACTTGACTGATTTTTTGTATTTTTAGTAGAGAC GAATAGCTGGGACTGCAGGCACATGCCACCACGCTTGACTGATTTTTTGTATTTTTAGTAGAGAC A G RPL34 Ensembl:ENSG00000109475 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1338819735 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_356074 34332 RMVar_ID_34332 Human_SNP_ID_198240831 A-to-I Human chr4 + 108623645 108623645 108623645 GTTAGCCAGGATGGTCTCTATCTGACCTCATGATCTGTCAGCCTCGACCTCCCAAAGTGCTGGGA GTTAGCCAGGATGGTCTCTATCTGACCTCATGTTCTGTCAGCCTCGACCTCCCAAAGTGCTGGGA A T RPL34 Ensembl:ENSG00000109475 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1332036486 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_356074 34333 RMVar_ID_34333 Human_SNP_ID_198241342 A-to-I Human chr4 + 108625485 108625485 108625485 TCGGCTCACCGCACCCTCTGCCTTCCAGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGC TCGGCTCACCGCACCCTCTGCCTTCCAGGTTCGAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGC A G RPL34 Ensembl:ENSG00000109475 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1031533068 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_591194 34334 RMVar_ID_34334 Human_SNP_ID_198241369 A-to-I Human chr4 + 108625586 108625586 108625586 TTTGTATATTTTAGTAGAGACGAGGTTTCTCCATGTTGGTCAGGCTGGTCTCAAACTCCCGACCT TTTGTATATTTTAGTAGAGACGAGGTTTCTCCGTGTTGGTCAGGCTGGTCTCAAACTCCCGACCT A G RPL34 Ensembl:ENSG00000109475 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs965630409 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15234044 34335 RMVar_ID_34335 Human_SNP_ID_198241379 A-to-I Human chr4 + 108625625 108625625 108625625 TCAGGCTGGTCTCAAACTCCCGACCTCAGGTGATCTGCCCACCTCGGCCTCCCAAAGTGCTGGTG TCAGGCTGGTCTCAAACTCCCGACCTCAGGTGGTCTGCCCACCTCGGCCTCCCAAAGTGCTGGTG A G RPL34 Ensembl:ENSG00000109475 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1180148274 Functional Loss SNV dbSNP153 33..33 33 - - - 34336 RMVar_ID_34336 Human_SNP_ID_198241530 A-to-I Human chr4 + 108626234 108626234 108626234 TTGGCTTGCTGCAACCTCCACCTCCTGGACTCAAGTGATTCTCTGCCTCAGCCTCCCAAGTAGCT TTGGCTTGCTGCAACCTCCACCTCCTGGACTCTAGTGATTCTCTGCCTCAGCCTCCCAAGTAGCT A T RPL34 Ensembl:ENSG00000109475 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1267595256 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15021331 34337 RMVar_ID_34337 Human_SNP_ID_198241571 A-to-I Human chr4 + 108626390 108626390 108626390 GGGCTCAAGCAGTCTGCCTGCCTCAGCCTCCCAGCGTGCCAGGATTACAGGCATGAGCCATTCTT GGGCTCAAGCAGTCTGCCTGCCTCAGCCTCCCGGCGTGCCAGGATTACAGGCATGAGCCATTCTT A G RPL34 Ensembl:ENSG00000109475 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs56375323 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_3677,GWAS_ID_3678,GWAS_ID_3679,GWAS_ID_3680,GWAS_ID_3681,GWAS_ID_3682,GWAS_ID_3683,GWAS_ID_3684,GWAS_ID_3685,GWAS_ID_3686,GWAS_ID_3687 34338 RMVar_ID_34338 Human_SNP_ID_198241611 A-to-I Human chr4 + 108626470 108626468 108626470 GCTGACAACCTTTTTTTTTTTTTTTTTTTTTGAAATGGAGCCTTGCTCTTGCCCAGGCTGGAGCG GCTGACAACCTTTTTTTTTTTTTTTTTTTTT__AATGGAGCCTTGCTCTTGCCCAGGCTGGAGCG TGA T RPL34 Ensembl:ENSG00000109475 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1305760281 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_15021347 34339 RMVar_ID_34339 Human_SNP_ID_198241614 A-to-I Human chr4 + 108626470 108626470 108626470 GCTGACAACCTTTTTTTTTTTTTTTTTTTTTGAAATGGAGCCTTGCTCTTGCCCAGGCTGGAGCG GCTGACAACCTTTTTTTTTTTTTTTTTTTTTGTAATGGAGCCTTGCTCTTGCCCAGGCTGGAGCG A T RPL34 Ensembl:ENSG00000109475 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1486303553 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15021347 34340 RMVar_ID_34340 Human_SNP_ID_198241643 A-to-I Human chr4 + 108626578 108626561 108626578 TCAAGCAATTCTGCCTCAGCCTCCTGAGGATTACAGGCGCCCACCACCACACCCGGCTAATTTTT TCAAGCAATTCTGCCT_________________CAGGCGCCCACCACCACACCCGGCTAATTTTT TCAGCCTCCTGAGGATTA T RPL34 Ensembl:ENSG00000109475 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs900412249 Functional Loss DEL dbSNP153 17..33 33 - - - Human_RBP_ID_15021349 34341 RMVar_ID_34341 Human_SNP_ID_198241654 A-to-I Human chr4 + 108626613 108626613 108626613 GGCGCCCACCACCACACCCGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTTGCCATATTGG GGCGCCCACCACCACACCCGGCTAATTTTTGTGTTTTTAGTAGAGATGGGGTTTTGCCATATTGG A G RPL34 Ensembl:ENSG00000109475 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1194119593 Functional Loss SNV dbSNP153 33..33 33 - - - 34342 RMVar_ID_34342 Human_SNP_ID_198241657 A-to-I Human chr4 + 108626619 108626619 108626619 CACCACCACACCCGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTTGCCATATTGGCCAGGT CACCACCACACCCGGCTAATTTTTGTATTTTTGGTAGAGATGGGGTTTTGCCATATTGGCCAGGT A G RPL34 Ensembl:ENSG00000109475 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1214432699 Functional Loss SNV dbSNP153 33..33 33 - - - 34343 RMVar_ID_34343 Human_SNP_ID_198241662 A-to-I Human chr4 + 108626639 108626639 108626639 TTTTGTATTTTTAGTAGAGATGGGGTTTTGCCATATTGGCCAGGTTCATCTTGAACTCTTGATCT TTTTGTATTTTTAGTAGAGATGGGGTTTTGCCGTATTGGCCAGGTTCATCTTGAACTCTTGATCT A G RPL34 Ensembl:ENSG00000109475 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs536247784 Functional Loss SNV dbSNP153 33..33 33 - - - 34344 RMVar_ID_34344 Human_SNP_ID_198241767 A-to-I Human chr4 + 108627028 108627028 108627028 TTGGGAGGCCAAGGCGGGCGGATCATGAGGTCAGGAGATCGAGACCATCCTGTCTAGCACGGTGA TTGGGAGGCCAAGGCGGGCGGATCATGAGGTCGGGAGATCGAGACCATCCTGTCTAGCACGGTGA A G RPL34 Ensembl:ENSG00000109475 Protein coding intron GSE38233;GSE107867 cultured B-cells;ASD brains,temporal_cortex - 24183664,30559470 RNA-Seq:(High) rs1254228517 Functional Loss SNV dbSNP153 33..33 33 - - - 34345 RMVar_ID_34345 Human_SNP_ID_198241790 A-to-I Human chr4 + 108627082 108627082 108627082 TAGCACGGTGAAACCCCGTCTGTACTAAAAATACAAAAAACTAGCTGGGCGTGGTGGTATGCGTC TAGCACGGTGAAACCCCGTCTGTACTAAAAATGCAAAAAACTAGCTGGGCGTGGTGGTATGCGTC A G RPL34 Ensembl:ENSG00000109475 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1205890400 Functional Loss SNV dbSNP153 33..33 33 - - - 34346 RMVar_ID_34346 Human_SNP_ID_198241794 A-to-I Human chr4 + 108627092 108627092 108627092 AAACCCCGTCTGTACTAAAAATACAAAAAACTAGCTGGGCGTGGTGGTATGCGTCTGTAATCCCA AAACCCCGTCTGTACTAAAAATACAAAAAACTGGCTGGGCGTGGTGGTATGCGTCTGTAATCCCA A G RPL34 Ensembl:ENSG00000109475 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1348408102 Functional Loss SNV dbSNP153 33..33 33 - - - 34347 RMVar_ID_34347 Human_SNP_ID_198241816 A-to-I Human chr4 + 108627159 108627159 108627159 TACTCGGGAGGCTGAGGCAAGAGGATTGCTTGAACCCGGGAGGCAGAGGTTGCAGTAAGCCAAGA TACTCGGGAGGCTGAGGCAAGAGGATTGCTTGCACCCGGGAGGCAGAGGTTGCAGTAAGCCAAGA A C RPL34 Ensembl:ENSG00000109475 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1399340890 Functional Loss SNV dbSNP153 33..33 33 - - - 34348 RMVar_ID_34348 Human_SNP_ID_198241866 A-to-I Human chr4 + 108627286 108627286 108627286 TTTTCTTAGGCCAGACCCAGTGGCTCACCCCTATAGTCCCAGTCTCAACACTTGGGATGCTGAGG TTTTCTTAGGCCAGACCCAGTGGCTCACCCCTGTAGTCCCAGTCTCAACACTTGGGATGCTGAGG A G RPL34 Ensembl:ENSG00000109475 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs963463103 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15021369 34349 RMVar_ID_34349 Human_SNP_ID_198241951 A-to-I Human chr4 + 108627598 108627598 108627598 TTTAAGAATTTAACCGCCAGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAG TTTAAGAATTTAACCGCCAGGCGCGGTGGCTCCCGCCTGTAATCCCAGCACTTTGGGAGGCTGAG A C RPL34 Ensembl:ENSG00000109475 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1560615060 Functional Loss SNV dbSNP153 33..33 33 - - - 34350 RMVar_ID_34350 Human_SNP_ID_198241954 A-to-I Human chr4 + 108627606 108627606 108627606 TTTAACCGCCAGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGTGG TTTAACCGCCAGGCGCGGTGGCTCACGCCTGTGATCCCAGCACTTTGGGAGGCTGAGGCAGGTGG A G RPL34 Ensembl:ENSG00000109475 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1037684873 Functional Loss SNV dbSNP153 33..33 33 - - - 34351 RMVar_ID_34351 Human_SNP_ID_198242325 A-to-I Human chr4 + 108629018 108629018 108629018 ATTTTTGTATTTTTAGTAGAGACGGGTTCGCCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCT ATTTTTGTATTTTTAGTAGAGACGGGTTCGCCCTGTTGGCCAGGCTGGTCTCGAACTCCTGACCT A C RPL34 Ensembl:ENSG00000109475 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1018713280 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15021436,Human_RBP_ID_25775719 34352 RMVar_ID_34352 Human_SNP_ID_198242326 A-to-I Human chr4 + 108629018 108629018 108629018 ATTTTTGTATTTTTAGTAGAGACGGGTTCGCCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCT ATTTTTGTATTTTTAGTAGAGACGGGTTCGCCGTGTTGGCCAGGCTGGTCTCGAACTCCTGACCT A G RPL34 Ensembl:ENSG00000109475 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1018713280 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15021436,Human_RBP_ID_25775719 34353 RMVar_ID_34353 Human_SNP_ID_198242350 A-to-I Human chr4 + 108629092 108629092 108629092 CGCCCGCCTCGGCCTGCTAAAGTGTTGGGATGACAGGCTTGAGCCACCACGCTGGGCCACTACTC CGCCCGCCTCGGCCTGCTAAAGTGTTGGGATGGCAGGCTTGAGCCACCACGCTGGGCCACTACTC A G RPL34 Ensembl:ENSG00000109475 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1048112256 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15021438 34354 RMVar_ID_34354 Human_SNP_ID_198242717 A-to-I Human chr4 + 108630691 108630691 108630691 AAACCCCGTCTCTACTAAAAATACAAAAAATTAGCCGGGCATGGTGGCAGGCGCCTGTAGTCACA AAACCCCGTCTCTACTAAAAATACAAAAAATTGGCCGGGCATGGTGGCAGGCGCCTGTAGTCACA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs895165888 Functional Loss SNV dbSNP153 33..33 33 - - - 34355 RMVar_ID_34355 Human_SNP_ID_198243589 A-to-I Human chr4 + 108634051 108634051 108634051 CACCCGCCTTGGCCTCCCAAATTGCTGGGATTACAGACATGAGCCACCGCGCCCGGCCCTACAAT CACCCGCCTTGGCCTCCCAAATTGCTGGGATTTCAGACATGAGCCACCGCGCCCGGCCCTACAAT A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs986099372 Functional Loss SNV dbSNP153 33..33 33 - - - 34356 RMVar_ID_34356 Human_SNP_ID_198249947 A-to-I Human chr4 + 108659216 108659216 108659216 GTTGGCCAGGCTGTTCTGGAACGCTTGACTTCATGATCGACCCGCCTCAGCCTCCCAAAGTGCTG GTTGGCCAGGCTGTTCTGGAACGCTTGACTTCGTGATCGACCCGCCTCAGCCTCCCAAAGTGCTG A G OSTC Ensembl:ENSG00000198856 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1476808070 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104578,RMVar_hsa_circ_107374,RMVar_hsa_circ_227921,RMVar_hsa_circ_227923 34357 RMVar_ID_34357 Human_SNP_ID_198249956 A-to-I Human chr4 + 108659240 108659240 108659240 TTGACTTCATGATCGACCCGCCTCAGCCTCCCAAAGTGCTGGGATTATAGGTGTGAGCCACTGTG TTGACTTCATGATCGACCCGCCTCAGCCTCCCCAAGTGCTGGGATTATAGGTGTGAGCCACTGTG A C OSTC Ensembl:ENSG00000198856 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs543939811 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104578,RMVar_hsa_circ_107374,RMVar_hsa_circ_227921,RMVar_hsa_circ_227923 34358 RMVar_ID_34358 Human_SNP_ID_198250040 A-to-I Human chr4 + 108659596 108659596 108659596 CAAAACCATCCTGGCTAACATGGTGAAACCCCATCTCTTACTAAAAATACAAAAAATGAGCCAGG CAAAACCATCCTGGCTAACATGGTGAAACCCCGTCTCTTACTAAAAATACAAAAAATGAGCCAGG A G OSTC Ensembl:ENSG00000198856 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1319358417 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104578,RMVar_hsa_circ_107374,RMVar_hsa_circ_227921,RMVar_hsa_circ_227923 34359 RMVar_ID_34359 Human_SNP_ID_198250206 A-to-I Human chr4 + 108660261 108660261 108660261 AAACAGGACAGTGGTCCAAACAGAAAATTGCTATTTTCTGTATCTTGTAAATCTAGGATTTGAGT AAACAGGACAGTGGTCCAAACAGAAAATTGCTCTTTTCTGTATCTTGTAAATCTAGGATTTGAGT A C OSTC Ensembl:ENSG00000198856 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6818080 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_3688,GWAS_ID_3689,GWAS_ID_3690,GWAS_ID_3691,GWAS_ID_3692,GWAS_ID_3693,GWAS_ID_3694,GWAS_ID_3695,GWAS_ID_3696,GWAS_ID_3697,GWAS_ID_3698,GWAS_ID_3699,GWAS_ID_3700,GWAS_ID_3701,GWAS_ID_3702,GWAS_ID_3703,GWAS_ID_3704,GWAS_ID_3705,GWAS_ID_3706,GWAS_ID_3707,GWAS_ID_3708,GWAS_ID_3709,GWAS_ID_3710,GWAS_ID_3711,GWAS_ID_3712,GWAS_ID_3713,GWAS_ID_3714,GWAS_ID_3715,GWAS_ID_3716,GWAS_ID_3717,GWAS_ID_3718,GWAS_ID_3719,GWAS_ID_3720,GWAS_ID_3721,GWAS_ID_3722,GWAS_ID_3723,GWAS_ID_3724,GWAS_ID_3725,GWAS_ID_3726,GWAS_ID_3727,GWAS_ID_3728,GWAS_ID_3729,GWAS_ID_3730,GWAS_ID_3731,GWAS_ID_3732,GWAS_ID_3733,GWAS_ID_3734,GWAS_ID_3735,GWAS_ID_3736,GWAS_ID_3737,GWAS_ID_3738,GWAS_ID_3739,GWAS_ID_3740,GWAS_ID_3741,GWAS_ID_3742,GWAS_ID_3743,GWAS_ID_3744,GWAS_ID_3745,GWAS_ID_3746,GWAS_ID_3747,GWAS_ID_3748,GWAS_ID_3749,GWAS_ID_3750,GWAS_ID_3751,GWAS_ID_3752,GWAS_ID_3753,GWAS_ID_3754,GWAS_ID_3755,GWAS_ID_3756,GWAS_ID_3757,GWAS_ID_3758,GWAS_ID_3759,GWAS_ID_3760,GWAS_ID_3761,GWAS_ID_3762,GWAS_ID_3763,GWAS_ID_3764,GWAS_ID_3765,GWAS_ID_3766,GWAS_ID_3767,GWAS_ID_3768,GWAS_ID_3769,GWAS_ID_3770,GWAS_ID_3771,GWAS_ID_3772,GWAS_ID_3773,GWAS_ID_3774 RMVar_hsa_circ_104578,RMVar_hsa_circ_107374,RMVar_hsa_circ_227921,RMVar_hsa_circ_227923 34360 RMVar_ID_34360 Human_SNP_ID_198250207 A-to-I Human chr4 + 108660261 108660261 108660261 AAACAGGACAGTGGTCCAAACAGAAAATTGCTATTTTCTGTATCTTGTAAATCTAGGATTTGAGT AAACAGGACAGTGGTCCAAACAGAAAATTGCTGTTTTCTGTATCTTGTAAATCTAGGATTTGAGT A G OSTC Ensembl:ENSG00000198856 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6818080 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_3688,GWAS_ID_3689,GWAS_ID_3690,GWAS_ID_3691,GWAS_ID_3692,GWAS_ID_3693,GWAS_ID_3694,GWAS_ID_3695,GWAS_ID_3696,GWAS_ID_3697,GWAS_ID_3698,GWAS_ID_3699,GWAS_ID_3700,GWAS_ID_3701,GWAS_ID_3702,GWAS_ID_3703,GWAS_ID_3704,GWAS_ID_3705,GWAS_ID_3706,GWAS_ID_3707,GWAS_ID_3708,GWAS_ID_3709,GWAS_ID_3710,GWAS_ID_3711,GWAS_ID_3712,GWAS_ID_3713,GWAS_ID_3714,GWAS_ID_3715,GWAS_ID_3716,GWAS_ID_3717,GWAS_ID_3718,GWAS_ID_3719,GWAS_ID_3720,GWAS_ID_3721,GWAS_ID_3722,GWAS_ID_3723,GWAS_ID_3724,GWAS_ID_3725,GWAS_ID_3726,GWAS_ID_3727,GWAS_ID_3728,GWAS_ID_3729,GWAS_ID_3730,GWAS_ID_3731,GWAS_ID_3732,GWAS_ID_3733,GWAS_ID_3734,GWAS_ID_3735,GWAS_ID_3736,GWAS_ID_3737,GWAS_ID_3738,GWAS_ID_3739,GWAS_ID_3740,GWAS_ID_3741,GWAS_ID_3742,GWAS_ID_3743,GWAS_ID_3744,GWAS_ID_3745,GWAS_ID_3746,GWAS_ID_3747,GWAS_ID_3748,GWAS_ID_3749,GWAS_ID_3750,GWAS_ID_3751,GWAS_ID_3752,GWAS_ID_3753,GWAS_ID_3754,GWAS_ID_3755,GWAS_ID_3756,GWAS_ID_3757,GWAS_ID_3758,GWAS_ID_3759,GWAS_ID_3760,GWAS_ID_3761,GWAS_ID_3762,GWAS_ID_3763,GWAS_ID_3764,GWAS_ID_3765,GWAS_ID_3766,GWAS_ID_3767,GWAS_ID_3768,GWAS_ID_3769,GWAS_ID_3770,GWAS_ID_3771,GWAS_ID_3772,GWAS_ID_3773,GWAS_ID_3774 RMVar_hsa_circ_104578,RMVar_hsa_circ_107374,RMVar_hsa_circ_227921,RMVar_hsa_circ_227923 34361 RMVar_ID_34361 Human_SNP_ID_198250392 A-to-I Human chr4 + 108661055 108661055 108661055 CCTGGTCAACGTGGTGAAAACCAGTCTCTACTAAAAAATAAAAAAATTAGCTGGGCGTGGTAGTG CCTGGTCAACGTGGTGAAAACCAGTCTCTACTGAAAAATAAAAAAATTAGCTGGGCGTGGTAGTG A G OSTC Ensembl:ENSG00000198856 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1252145074 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104578,RMVar_hsa_circ_107374,RMVar_hsa_circ_227921,RMVar_hsa_circ_227923 34362 RMVar_ID_34362 Human_SNP_ID_198250918 A-to-I Human chr4 + 108663289 108663289 108663289 GCTGGAGTGCAGTGGCGTGATCTCGGCTCACTACAAACTCTGCCTCCCAGGTACATACCATTCTC GCTGGAGTGCAGTGGCGTGATCTCGGCTCACTGCAAACTCTGCCTCCCAGGTACATACCATTCTC A G OSTC Ensembl:ENSG00000198856 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs376856124 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_591246,Human_Splice_Rec_591247 RMVar_hsa_circ_104578,RMVar_hsa_circ_107374,RMVar_hsa_circ_227921,RMVar_hsa_circ_227923 34363 RMVar_ID_34363 Human_SNP_ID_198251267 A-to-I Human chr4 + 108664739 108664739 108664739 CCTCGGCGTCCTGAGTAGCTGGGACTACAGGCATGCACTACCACACCCAGGTAATTTTTGTATTT CCTCGGCGTCCTGAGTAGCTGGGACTACAGGCGTGCACTACCACACCCAGGTAATTTTTGTATTT A G OSTC Ensembl:ENSG00000198856 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11943458 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_3775,GWAS_ID_3776,GWAS_ID_3777,GWAS_ID_3778,GWAS_ID_3779,GWAS_ID_3780,GWAS_ID_3781,GWAS_ID_3782,GWAS_ID_3783,GWAS_ID_3784,GWAS_ID_3785,GWAS_ID_3786,GWAS_ID_3787,GWAS_ID_3788,GWAS_ID_3789,GWAS_ID_3790,GWAS_ID_3791,GWAS_ID_3792,GWAS_ID_3793,GWAS_ID_3794,GWAS_ID_3795,GWAS_ID_3796,GWAS_ID_3797,GWAS_ID_3798,GWAS_ID_3799,GWAS_ID_3800,GWAS_ID_3801,GWAS_ID_3802,GWAS_ID_3803,GWAS_ID_3804,GWAS_ID_3805,GWAS_ID_3806,GWAS_ID_3807,GWAS_ID_3808,GWAS_ID_3809,GWAS_ID_3810,GWAS_ID_3811,GWAS_ID_3812,GWAS_ID_3813,GWAS_ID_3814,GWAS_ID_3815,GWAS_ID_3816,GWAS_ID_3817,GWAS_ID_3818,GWAS_ID_3819,GWAS_ID_3820,GWAS_ID_3821,GWAS_ID_3822,GWAS_ID_3823,GWAS_ID_3824,GWAS_ID_3825,GWAS_ID_3826,GWAS_ID_3827,GWAS_ID_3828,GWAS_ID_3829,GWAS_ID_3830,GWAS_ID_3831,GWAS_ID_3832,GWAS_ID_3833,GWAS_ID_3834,GWAS_ID_3835,GWAS_ID_3836,GWAS_ID_3837,GWAS_ID_3838,GWAS_ID_3839,GWAS_ID_3840,GWAS_ID_3841,GWAS_ID_3842,GWAS_ID_3843,GWAS_ID_3844,GWAS_ID_3845,GWAS_ID_3846,GWAS_ID_3847,GWAS_ID_3848,GWAS_ID_3849,GWAS_ID_3850,GWAS_ID_3851,GWAS_ID_3852,GWAS_ID_3853,GWAS_ID_3854,GWAS_ID_3855,GWAS_ID_3856,GWAS_ID_3857,GWAS_ID_3858,GWAS_ID_3859,GWAS_ID_3860,GWAS_ID_3861 RMVar_hsa_circ_104578,RMVar_hsa_circ_107374,RMVar_hsa_circ_227921,RMVar_hsa_circ_227923 34364 RMVar_ID_34364 Human_SNP_ID_198251695 A-to-I Human chr4 + 108666454 108666454 108666454 GGGAAGGGCCAGGCGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGATGG GGGAAGGGCCAGGCGCGGTGGCTCACACCTGTCATCCCAGCACTTTGGGAGGCCGAGGTGGATGG A C OSTC Ensembl:ENSG00000198856 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs149995900 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104578,RMVar_hsa_circ_107374,RMVar_hsa_circ_227921,RMVar_hsa_circ_227923 34365 RMVar_ID_34365 Human_SNP_ID_198429641 A-to-I Human chr4 - 109426439 109426439 109426439 AGTAGAAGGGGCAGGTGTGGTGGCTCATGCCTATAATCCCAGGACTTTGGGAGGCCAAAGCAGGA AGTAGAAGGGGCAGGTGTGGTGGCTCATGCCTGTAATCCCAGGACTTTGGGAGGCCAAAGCAGGA T C SEC24B-AS1 Ensembl:ENSG00000247950 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1183268133 Functional Loss SNV dbSNP153 33..33 33 - - - 34366 RMVar_ID_34366 Human_SNP_ID_198450194 A-to-I Human chr4 + 109508296 109508296 109508296 TAGGTAAATGTAGCGTATGGGCCATGCATAGTAGCTCACGGCTGTAATTCCAGCACTTTGGGAAG TAGGTAAATGTAGCGTATGGGCCATGCATAGTGGCTCACGGCTGTAATTCCAGCACTTTGGGAAG A G SEC24B Ensembl:ENSG00000138802 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1414633483 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114072,RMVar_hsa_circ_121412,RMVar_hsa_circ_266148,RMVar_hsa_circ_227936,RMVar_hsa_circ_98006,RMVar_hsa_circ_34279,RMVar_hsa_circ_4514,RMVar_hsa_circ_106411,RMVar_hsa_circ_227940,RMVar_hsa_circ_227941,RMVar_hsa_circ_337682,RMVar_hsa_circ_323496,RMVar_hsa_circ_62885,RMVar_hsa_circ_345991,RMVar_hsa_circ_227946,RMVar_hsa_circ_227947,RMVar_hsa_circ_364468,RMVar_hsa_circ_364743,RMVar_hsa_circ_347936,RMVar_hsa_circ_312543,RMVar_hsa_circ_331981,RMVar_hsa_circ_277040,RMVar_hsa_circ_271828,RMVar_hsa_circ_125361,RMVar_hsa_circ_227951,RMVar_hsa_circ_227955,RMVar_hsa_circ_77323,RMVar_hsa_circ_81610,RMVar_hsa_circ_227957,RMVar_hsa_circ_74716,RMVar_hsa_circ_227956,RMVar_hsa_circ_227953,RMVar_hsa_circ_227954,RMVar_hsa_circ_227952,RMVar_hsa_circ_227949,RMVar_hsa_circ_227950,RMVar_hsa_circ_227948,RMVar_hsa_circ_341893,RMVar_hsa_circ_314489,RMVar_hsa_circ_3808,RMVar_hsa_circ_28656,RMVar_hsa_circ_312263,RMVar_hsa_circ_227962,RMVar_hsa_circ_227963,RMVar_hsa_circ_353728,RMVar_hsa_circ_356399,RMVar_hsa_circ_316402,RMVar_hsa_circ_64662,RMVar_hsa_circ_308396,RMVar_hsa_circ_40876,RMVar_hsa_circ_26291,RMVar_hsa_circ_227964,RMVar_hsa_circ_227966,RMVar_hsa_circ_227967,RMVar_hsa_circ_227965,RMVar_hsa_circ_28739,RMVar_hsa_circ_361368,RMVar_hsa_circ_20728,RMVar_hsa_circ_227968 34367 RMVar_ID_34367 Human_SNP_ID_198450227 A-to-I Human chr4 + 109508430 109508430 109508430 CCTCCAAAAAAACAAAAAAATTAGCTGAGCATAGTGCCATGTGCCTGTGGTCCCAGCTACTCTGT CCTCCAAAAAAACAAAAAAATTAGCTGAGCATGGTGCCATGTGCCTGTGGTCCCAGCTACTCTGT A G SEC24B Ensembl:ENSG00000138802 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1038893071 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114072,RMVar_hsa_circ_121412,RMVar_hsa_circ_266148,RMVar_hsa_circ_227936,RMVar_hsa_circ_98006,RMVar_hsa_circ_34279,RMVar_hsa_circ_4514,RMVar_hsa_circ_106411,RMVar_hsa_circ_227940,RMVar_hsa_circ_227941,RMVar_hsa_circ_337682,RMVar_hsa_circ_323496,RMVar_hsa_circ_62885,RMVar_hsa_circ_345991,RMVar_hsa_circ_227946,RMVar_hsa_circ_227947,RMVar_hsa_circ_364468,RMVar_hsa_circ_364743,RMVar_hsa_circ_347936,RMVar_hsa_circ_312543,RMVar_hsa_circ_331981,RMVar_hsa_circ_277040,RMVar_hsa_circ_271828,RMVar_hsa_circ_125361,RMVar_hsa_circ_227951,RMVar_hsa_circ_227955,RMVar_hsa_circ_77323,RMVar_hsa_circ_81610,RMVar_hsa_circ_227957,RMVar_hsa_circ_74716,RMVar_hsa_circ_227956,RMVar_hsa_circ_227953,RMVar_hsa_circ_227954,RMVar_hsa_circ_227952,RMVar_hsa_circ_227949,RMVar_hsa_circ_227950,RMVar_hsa_circ_227948,RMVar_hsa_circ_341893,RMVar_hsa_circ_314489,RMVar_hsa_circ_3808,RMVar_hsa_circ_28656,RMVar_hsa_circ_312263,RMVar_hsa_circ_227962,RMVar_hsa_circ_227963,RMVar_hsa_circ_353728,RMVar_hsa_circ_356399,RMVar_hsa_circ_316402,RMVar_hsa_circ_64662,RMVar_hsa_circ_308396,RMVar_hsa_circ_40876,RMVar_hsa_circ_26291,RMVar_hsa_circ_227964,RMVar_hsa_circ_227966,RMVar_hsa_circ_227967,RMVar_hsa_circ_227965,RMVar_hsa_circ_28739,RMVar_hsa_circ_361368,RMVar_hsa_circ_20728,RMVar_hsa_circ_227968 34368 RMVar_ID_34368 Human_SNP_ID_198450450 A-to-I Human chr4 + 109509418 109509418 109509418 TTATTTGGCCAGGCACAGTGGCTCACGCCTGTAATCCTAGCACTTTGGAAGGCCGAGGCAGGCGG TTATTTGGCCAGGCACAGTGGCTCACGCCTGTGATCCTAGCACTTTGGAAGGCCGAGGCAGGCGG A G SEC24B Ensembl:ENSG00000138802 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1301807698 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114072,RMVar_hsa_circ_121412,RMVar_hsa_circ_266148,RMVar_hsa_circ_227936,RMVar_hsa_circ_98006,RMVar_hsa_circ_34279,RMVar_hsa_circ_4514,RMVar_hsa_circ_106411,RMVar_hsa_circ_227940,RMVar_hsa_circ_227941,RMVar_hsa_circ_337682,RMVar_hsa_circ_323496,RMVar_hsa_circ_62885,RMVar_hsa_circ_345991,RMVar_hsa_circ_227946,RMVar_hsa_circ_227947,RMVar_hsa_circ_364468,RMVar_hsa_circ_364743,RMVar_hsa_circ_347936,RMVar_hsa_circ_312543,RMVar_hsa_circ_331981,RMVar_hsa_circ_277040,RMVar_hsa_circ_271828,RMVar_hsa_circ_125361,RMVar_hsa_circ_227951,RMVar_hsa_circ_227955,RMVar_hsa_circ_77323,RMVar_hsa_circ_81610,RMVar_hsa_circ_227957,RMVar_hsa_circ_74716,RMVar_hsa_circ_227956,RMVar_hsa_circ_227953,RMVar_hsa_circ_227954,RMVar_hsa_circ_227952,RMVar_hsa_circ_227949,RMVar_hsa_circ_227950,RMVar_hsa_circ_227948,RMVar_hsa_circ_341893,RMVar_hsa_circ_314489,RMVar_hsa_circ_3808,RMVar_hsa_circ_28656,RMVar_hsa_circ_312263,RMVar_hsa_circ_227962,RMVar_hsa_circ_227963,RMVar_hsa_circ_353728,RMVar_hsa_circ_356399,RMVar_hsa_circ_316402,RMVar_hsa_circ_64662,RMVar_hsa_circ_308396,RMVar_hsa_circ_40876,RMVar_hsa_circ_26291,RMVar_hsa_circ_227964,RMVar_hsa_circ_227966,RMVar_hsa_circ_227967,RMVar_hsa_circ_227965,RMVar_hsa_circ_28739,RMVar_hsa_circ_361368,RMVar_hsa_circ_20728,RMVar_hsa_circ_227968 34369 RMVar_ID_34369 Human_SNP_ID_198491568 A-to-I Human chr4 - 109676672 109676672 109676672 TCTTGTGCTATTCTGCTATTGCAGCAGAAAACAGATTAAGACAGAAAATTGGTACTAGGAGCAGA TCTTGTGCTATTCTGCTATTGCAGCAGAAAACGGATTAAGACAGAAAATTGGTACTAGGAGCAGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984802660 Functional Loss SNV dbSNP153 33..33 33 - - - 34370 RMVar_ID_34370 Human_SNP_ID_198494554 A-to-I Human chr4 - 109687789 109687789 109687789 CAGCAGCCACCGTTGCTTTGATAGACGCATACAAGCCCTTTCTAACATTAGCAAGTCATAAAAAT CAGCAGCCACCGTTGCTTTGATAGACGCATACCAGCCCTTTCTAACATTAGCAAGTCATAAAAAT T G - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1561254771 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8582447 34371 RMVar_ID_34371 Human_SNP_ID_198494955 A-to-I Human chr4 - 109689104 109689104 109689104 AGGCATGGCGGCGCATGCCTGCAATCCCAGCTACTTGGAAGGCTGAGGCAGGAGAATCACTTGAA AGGCATGGCGGCGCATGCCTGCAATCCCAGCTTCTTGGAAGGCTGAGGCAGGAGAATCACTTGAA T A CASP6 Ensembl:ENSG00000138794 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs930459502 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_611402 34372 RMVar_ID_34372 Human_SNP_ID_198494957 A-to-I Human chr4 - 109689108 109689108 109689108 AGCTAGGCATGGCGGCGCATGCCTGCAATCCCAGCTACTTGGAAGGCTGAGGCAGGAGAATCACT AGCTAGGCATGGCGGCGCATGCCTGCAATCCCTGCTACTTGGAAGGCTGAGGCAGGAGAATCACT T A CASP6 Ensembl:ENSG00000138794 Protein coding 3'UTR GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1050308449 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_611402 34373 RMVar_ID_34373 Human_SNP_ID_198494958 A-to-I Human chr4 - 109689114 109689114 109689114 AAATTTAGCTAGGCATGGCGGCGCATGCCTGCAATCCCAGCTACTTGGAAGGCTGAGGCAGGAGA AAATTTAGCTAGGCATGGCGGCGCATGCCTGCCATCCCAGCTACTTGGAAGGCTGAGGCAGGAGA T G CASP6 Ensembl:ENSG00000138794 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1408253527 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_611402 34374 RMVar_ID_34374 Human_SNP_ID_198497845 A-to-I Human chr4 - 109700520 109700520 109700520 TTTGAAACTGAATGTATTAAGAGATGGGGTCTAGCTCTGTTACCCAGGCTGGAGTATGGTGACTA TTTGAAACTGAATGTATTAAGAGATGGGGTCTTGCTCTGTTACCCAGGCTGGAGTATGGTGACTA T A CASP6 Ensembl:ENSG00000138794 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs935214001 Functional Loss SNV dbSNP153 33..33 33 - - - 34375 RMVar_ID_34375 Human_SNP_ID_198504749 A-to-I Human chr4 - 109727793 109727793 109727793 TTATTTTATTTTTTGTTAATATTTTTGAGGCAAGGTCTCCCTCTGTGCCCAGGCTAGAGGGCAGT TTATTTTATTTTTTGTTAATATTTTTGAGGCAGGGTCTCCCTCTGTGCCCAGGCTAGAGGGCAGT T C PLA2G12A,AC126283.2 Ensembl:ENSG00000123739,Ensembl:ENSG00000285330 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985684657 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266915 34376 RMVar_ID_34376 Human_SNP_ID_198555260 A-to-I Human chr4 + 109925383 109925383 109925383 ATATCACAGCGTATGGTTGTTTTCTAGAAAGTAATAGCCAAAATTTACTGGGAACTCACTATGTG ATATCACAGCGTATGGTTGTTTTCTAGAAAGTGATAGCCAAAATTTACTGGGAACTCACTATGTG A G EGF Ensembl:ENSG00000138798 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs976371086 Functional Loss SNV dbSNP153 33..33 33 - - - 34377 RMVar_ID_34377 Human_SNP_ID_198606266 A-to-I Human chr4 - 110134742 110134742 110134742 TTGTCCAGGCTGGTCTCGAATTCCTGGCCTCAAGTGATCCTCCTACCTCAACTCCCAAAGTGCTG TTGTCCAGGCTGGTCTCGAATTCCTGGCCTCACGTGATCCTCCTACCTCAACTCCCAAAGTGCTG T G ELOVL6 Ensembl:ENSG00000170522 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs558512009 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_317199,RMVar_hsa_circ_309808 34378 RMVar_ID_34378 Human_SNP_ID_198617692 A-to-I Human chr4 - 110183930 110183930 110183930 TTGCCTAGGCTGGAGTACAGTGGTACGATCTCAGCTCACTGCAACGTCTGCCTCCCAGTCTAAAG TTGCCTAGGCTGGAGTACAGTGGTACGATCTCGGCTCACTGCAACGTCTGCCTCCCAGTCTAAAG T C ELOVL6 Ensembl:ENSG00000170522 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs535636799 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_317199,RMVar_hsa_circ_309808 34379 RMVar_ID_34379 Human_SNP_ID_198635667 A-to-I Human chr4 - 110252047 110252047 110252047 GAATGAGCAGGAACTCACCTCAGTGGTGCAGAAACTCCTGCAGCAGATCCAAGATAAATTTCAGA GAATGAGCAGGAACTCACCTCAGTGGTGCAGACACTCCTGCAGCAGATCCAAGATAAATTTCAGA T G HSBP1P2 Ensembl:ENSG00000166530 Pseudogene exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1371313757 Functional Loss SNV dbSNP153 33..33 33 - - - 34380 RMVar_ID_34380 Human_SNP_ID_198635669 A-to-I Human chr4 - 110252058 110252058 110252058 ACTGACCCCAAGAATGAGCAGGAACTCACCTCAGTGGTGCAGAAACTCCTGCAGCAGATCCAAGA ACTGACCCCAAGAATGAGCAGGAACTCACCTCGGTGGTGCAGAAACTCCTGCAGCAGATCCAAGA T C HSBP1P2 Ensembl:ENSG00000166530 Pseudogene exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1327460901 Functional Loss SNV dbSNP153 33..33 33 - - - 34381 RMVar_ID_34381 Human_SNP_ID_199126868 A-to-I Human chr4 - 112281734 112281730 112281734 CTGCTCCTTGTGGGAACTGCTGATGTTTTGACAAAAGAAAGAGGGAAGGTGGAACTACACAGTGG CTGCTCCTTGTGGGAACTGCTGATGTTTTGAC____GAAAGAGGGAAGGTGGAACTACACAGTGG CTTTT C TIFA Ensembl:ENSG00000145365 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10547838 Functional Loss DEL dbSNP153 33..36 33 - - - Human_Splice_Rec_592935 34382 RMVar_ID_34382 Human_SNP_ID_199126870 A-to-I Human chr4 - 112281734 112281734 112281734 CTGCTCCTTGTGGGAACTGCTGATGTTTTGACAAAAGAAAGAGGGAAGGTGGAACTACACAGTGG CTGCTCCTTGTGGGAACTGCTGATGTTTTGACGAAAGAAAGAGGGAAGGTGGAACTACACAGTGG T C TIFA Ensembl:ENSG00000145365 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs201769691 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_592935 34383 RMVar_ID_34383 Human_SNP_ID_199148137 A-to-I Human chr4 + 112375249 112375249 112375249 GTCACTCAGCCGGAGTGTAGAGGTGCAGTCACAGCTCACTCCAGCCTCAATCTCCTGGGCTCAAG GTCACTCAGCCGGAGTGTAGAGGTGCAGTCACGGCTCACTCCAGCCTCAATCTCCTGGGCTCAAG A G ALPK1 Ensembl:ENSG00000073331 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1169506107 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_228007,RMVar_hsa_circ_108897 34384 RMVar_ID_34384 Human_SNP_ID_199167096 A-to-I Human chr4 + 112455959 112455959 112455959 GAGTCTCCCGGAGGAAATGACAATTACCTGACAATCACAGGGCCGTCACACCTCTTCCTGTCAGG GAGTCTCCCGGAGGAAATGACAATTACCTGACGATCACAGGGCCGTCACACCTCTTCCTGTCAGG A G TOX4P1 Ensembl:ENSG00000248697 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs953551291 Functional Loss SNV dbSNP153 33..33 33 - - - 34385 RMVar_ID_34385 Human_SNP_ID_199167103 A-to-I Human chr4 + 112455974 112455974 112455974 AATGACAATTACCTGACAATCACAGGGCCGTCACACCTCTTCCTGTCAGGGGCCGAGACATTCCA AATGACAATTACCTGACAATCACAGGGCCGTCGCACCTCTTCCTGTCAGGGGCCGAGACATTCCA A G TOX4P1 Ensembl:ENSG00000248697 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs911978967 Functional Loss SNV dbSNP153 33..33 33 - - - 34386 RMVar_ID_34386 Human_SNP_ID_199167116 A-to-I Human chr4 + 112456019 112456019 112456019 TCAGGGGCCGAGACATTCCATACACCAAGCTTAGGTGATGAAGAATTTGAAATCCCACCTATCTC TCAGGGGCCGAGACATTCCATACACCAAGCTTGGGTGATGAAGAATTTGAAATCCCACCTATCTC A G TOX4P1 Ensembl:ENSG00000248697 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1175198982 Functional Loss SNV dbSNP153 33..33 33 - - - 34387 RMVar_ID_34387 Human_SNP_ID_199167117 A-to-I Human chr4 + 112456019 112456019 112456019 TCAGGGGCCGAGACATTCCATACACCAAGCTTAGGTGATGAAGAATTTGAAATCCCACCTATCTC TCAGGGGCCGAGACATTCCATACACCAAGCTTTGGTGATGAAGAATTTGAAATCCCACCTATCTC A T TOX4P1 Ensembl:ENSG00000248697 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1175198982 Functional Loss SNV dbSNP153 33..33 33 - - - 34388 RMVar_ID_34388 Human_SNP_ID_199193718 A-to-I Human chr4 - 112562047 112562037 112562047 AAATTAGCTGGGCATACTGGCGCATGCCTGTAATCACAGCTATTCGGGAGGCTGAGGCAGGAGAA AAATTAGCTGGGCATACTGGCGCATGCCTGTA__________TTCGGGAGGCTGAGGCAGGAGAA ATAGCTGTGAT A ZGRF1 Ensembl:ENSG00000138658 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1177810703 Functional Loss DEL dbSNP153 33..42 33 - - - RMVar_hsa_circ_6485,RMVar_hsa_circ_345486,RMVar_hsa_circ_38280,RMVar_hsa_circ_302035,RMVar_hsa_circ_13883,RMVar_hsa_circ_228014,RMVar_hsa_circ_265075,RMVar_hsa_circ_94944,RMVar_hsa_circ_28177,RMVar_hsa_circ_39400,RMVar_hsa_circ_228015,RMVar_hsa_circ_42056,RMVar_hsa_circ_228016,RMVar_hsa_circ_98056,RMVar_hsa_circ_305762,RMVar_hsa_circ_297268,RMVar_hsa_circ_228017,RMVar_hsa_circ_360672,RMVar_hsa_circ_28888,RMVar_hsa_circ_228018 34389 RMVar_ID_34389 Human_SNP_ID_199202707 A-to-I Human chr4 - 112600509 112600509 112600509 TTTTGTATTTCTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCAGGACTCGAACTCCTGACCT TTTTGTATTTCTAGTAGAGACGGGGTTTCACCTTGTTGGCCAGGCAGGACTCGAACTCCTGACCT T A ZGRF1 Ensembl:ENSG00000138658 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1410319198 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265075,RMVar_hsa_circ_228021,RMVar_hsa_circ_292822,RMVar_hsa_circ_39400,RMVar_hsa_circ_28888,RMVar_hsa_circ_342141,RMVar_hsa_circ_330861,RMVar_hsa_circ_105251,RMVar_hsa_circ_281007,RMVar_hsa_circ_228023,RMVar_hsa_circ_228022,RMVar_hsa_circ_51122,RMVar_hsa_circ_228019,RMVar_hsa_circ_228020,RMVar_hsa_circ_73154,RMVar_hsa_circ_30869,RMVar_hsa_circ_46730,RMVar_hsa_circ_2763,RMVar_hsa_circ_70734,RMVar_hsa_circ_228031,RMVar_hsa_circ_94952,RMVar_hsa_circ_59203 34390 RMVar_ID_34390 Human_SNP_ID_199203826 A-to-I Human chr4 - 112605428 112605428 112605428 GGCCAGGCATGGTGACTCATGCCTGTAATCCCAGTACTTTGGGAGGCCAAGGCGGGTGGATCACT GGCCAGGCATGGTGACTCATGCCTGTAATCCCGGTACTTTGGGAGGCCAAGGCGGGTGGATCACT T C ZGRF1 Ensembl:ENSG00000138658 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs550549735 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265075,RMVar_hsa_circ_228021,RMVar_hsa_circ_292822,RMVar_hsa_circ_39400,RMVar_hsa_circ_28888,RMVar_hsa_circ_330861,RMVar_hsa_circ_105251,RMVar_hsa_circ_281007,RMVar_hsa_circ_228022,RMVar_hsa_circ_51122,RMVar_hsa_circ_228019,RMVar_hsa_circ_228020,RMVar_hsa_circ_30869,RMVar_hsa_circ_46730,RMVar_hsa_circ_2763,RMVar_hsa_circ_70734,RMVar_hsa_circ_228033,RMVar_hsa_circ_43939,RMVar_hsa_circ_228031,RMVar_hsa_circ_94952,RMVar_hsa_circ_346803,RMVar_hsa_circ_59203,RMVar_hsa_circ_345313,RMVar_hsa_circ_1527,RMVar_hsa_circ_228032 34391 RMVar_ID_34391 Human_SNP_ID_199208907 A-to-I Human chr4 - 112625206 112625206 112625206 TAGTTCACTGTAGCCTCAAACCCTTAGGCTCAAACAATCCTTCCGCCTTAGCTTCCGAAGTAGTT TAGTTCACTGTAGCCTCAAACCCTTAGGCTCAGACAATCCTTCCGCCTTAGCTTCCGAAGTAGTT T C ZGRF1 Ensembl:ENSG00000138658 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1406219151 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105251,RMVar_hsa_circ_228019,RMVar_hsa_circ_43939,RMVar_hsa_circ_370675,RMVar_hsa_circ_228037,RMVar_hsa_circ_103874,RMVar_hsa_circ_228038,RMVar_hsa_circ_116401,RMVar_hsa_circ_79786,RMVar_hsa_circ_228040,RMVar_hsa_circ_228043 34392 RMVar_ID_34392 Human_SNP_ID_199213529 A-to-I Human chr4 + 112644039 112644039 112644039 CGGAGGCGGGCAGATCACCAGGACAGCAATTCAAGACAAACCTGGCAAACATGGTGAAACCCCGT CGGAGGCGGGCAGATCACCAGGACAGCAATTCGAGACAAACCTGGCAAACATGGTGAAACCCCGT A G LARP7 Ensembl:ENSG00000174720 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6843988 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_228045,RMVar_hsa_circ_106189,RMVar_hsa_circ_228047,RMVar_hsa_circ_328373,RMVar_hsa_circ_228046 34393 RMVar_ID_34393 Human_SNP_ID_199213530 A-to-I Human chr4 + 112644039 112644039 112644039 CGGAGGCGGGCAGATCACCAGGACAGCAATTCAAGACAAACCTGGCAAACATGGTGAAACCCCGT CGGAGGCGGGCAGATCACCAGGACAGCAATTCTAGACAAACCTGGCAAACATGGTGAAACCCCGT A T LARP7 Ensembl:ENSG00000174720 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6843988 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_228045,RMVar_hsa_circ_106189,RMVar_hsa_circ_228047,RMVar_hsa_circ_328373,RMVar_hsa_circ_228046 34394 RMVar_ID_34394 Human_SNP_ID_199284561 A-to-I Human chr4 + 112937053 112937053 112937053 AACTCAAGCAATCCTCCCGCCTCTGCCTCCCAAAGTGCTGGAATCATAGACATGAGCCATCACGC AACTCAAGCAATCCTCCCGCCTCTGCCTCCCAGAGTGCTGGAATCATAGACATGAGCCATCACGC A G ANK2 Ensembl:ENSG00000145362 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs999680353 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_52888,RMVar_hsa_circ_96143,RMVar_hsa_circ_228053 34395 RMVar_ID_34395 Human_SNP_ID_199303876 A-to-I Human chr4 + 113020650 113020650 113020650 AGGAGTCCAAGACCAGCCTGGCAAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAATAGCC AGGAGTCCAAGACCAGCCTGGCAAACATGGTGCAACCCCGTCTCTACTAAAAATACAAAATAGCC A C ANK2 Ensembl:ENSG00000145362 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1336205104 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_52888,RMVar_hsa_circ_96143,RMVar_hsa_circ_228053 34396 RMVar_ID_34396 Human_SNP_ID_199397280 A-to-I Human chr4 - 113420414 113420414 113420414 ATGCAGTTGAGTTTCCCACATTTGGTGAAATCACAGGTGTCAGCACATCCAGAGTGCAATGGATA ATGCAGTTGAGTTTCCCACATTTGGTGAAATCCCAGGTGTCAGCACATCCAGAGTGCAATGGATA T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs927045103 Functional Loss SNV dbSNP153 33..33 33 - - - 34397 RMVar_ID_34397 Human_SNP_ID_199406736 A-to-I Human chr4 - 113453658 113453654 113453659 GGAGGCTGGCTAGTAGTGTGTGAGAAAAGAATAGAAGTGAAATTTGCATAATGAATGTAAAAGGG GGAGGCTGGCTAGTAGTGTGTGAGAAAAGAA_____GTGAAATTTGCATAATGAATGTAAAAGGG CTTCTA C CAMK2D Ensembl:ENSG00000145349 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1029232246 Functional Loss DEL dbSNP153 32..36 33 - - - Human_RBP_ID_611915,Human_RBP_ID_4770685,Human_RBP_ID_7259791,Human_RBP_ID_24031622,Human_RBP_ID_24431311,Human_RBP_ID_25777924 RMVar_hsa_circ_228137 34398 RMVar_ID_34398 Human_SNP_ID_199406741 A-to-I Human chr4 - 113453676 113453673 113453676 TCCCTTTTCCTTTTTTGGGGAGGCTGGCTAGTAGTGTGTGAGAAAAGAATAGAAGTGAAATTTGC TCCCTTTTCCTTTTTTGGGGAGGCTGGCTAGT___GTGTGAGAAAAGAATAGAAGTGAAATTTGC CACT C CAMK2D Ensembl:ENSG00000145349 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1195804873 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_611915,Human_RBP_ID_4770686,Human_RBP_ID_7259791,Human_RBP_ID_20989286,Human_RBP_ID_24031622,Human_RBP_ID_24431311,Human_RBP_ID_25829461 RMVar_hsa_circ_228137 34399 RMVar_ID_34399 Human_SNP_ID_200191624 A-to-I Human chr4 - 116599222 116599222 116599222 CAGGCCTTGAACCCCTCAGGCCCCAGCACCCCACCATGATCCTTGTCGAAGTGGTTGAAGGACGC CAGGCCTTGAACCCCTCAGGCCCCAGCACCCCGCCATGATCCTTGTCGAAGTGGTTGAAGGACGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878948535 Functional Loss SNV dbSNP153 33..33 33 - - - 34400 RMVar_ID_34400 Human_SNP_ID_200191627 A-to-I Human chr4 - 116599227 116599227 116599227 TGAGGCAGGCCTTGAACCCCTCAGGCCCCAGCACCCCACCATGATCCTTGTCGAAGTGGTTGAAG TGAGGCAGGCCTTGAACCCCTCAGGCCCCAGCGCCCCACCATGATCCTTGTCGAAGTGGTTGAAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879068125 Functional Loss SNV dbSNP153 33..33 33 - - - 34401 RMVar_ID_34401 Human_SNP_ID_200191631 A-to-I Human chr4 - 116599237 116599237 116599237 CCCAGGCTGATGAGGCAGGCCTTGAACCCCTCAGGCCCCAGCACCCCACCATGATCCTTGTCGAA CCCAGGCTGATGAGGCAGGCCTTGAACCCCTCGGGCCCCAGCACCCCACCATGATCCTTGTCGAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878994385 Functional Loss SNV dbSNP153 33..33 33 - - - 34402 RMVar_ID_34402 Human_SNP_ID_200191643 A-to-I Human chr4 - 116599273 116599273 116599273 TCGGCCTCACCCTGCCGGTCGTTCTCCACGTCATAGCCCAGGCTGATGAGGCAGGCCTTGAACCC TCGGCCTCACCCTGCCGGTCGTTCTCCACGTCGTAGCCCAGGCTGATGAGGCAGGCCTTGAACCC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879212717 Functional Loss SNV dbSNP153 33..33 33 - - - 34403 RMVar_ID_34403 Human_SNP_ID_200315243 A-to-I Human chr4 - 117084822 117084822 117084822 TCCTGAACTCTACTTCCAGAAAACCAAAAAACAAGACATCCCTCGTCAACTTGTCTACATTGGTC TCCTGAACTCTACTTCCAGAAAACCAAAAAACGAGACATCCCTCGTCAACTTGTCTACATTGGTC T C TRAM1L1 Ensembl:ENSG00000174599 Protein coding CDS GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs755408129 Functional Loss SNV dbSNP153 33..33 33 - - - 34404 RMVar_ID_34404 Human_SNP_ID_200590518 A-to-I Human chr4 - 118194019 118194019 118194019 AATATGAATTACACCTCAAGAGTTTTGAAAAGACCAAGGAGTCTTGGGAGATGAATTCAGAAGAG AATATGAATTACACCTCAAGAGTTTTGAAAAGTCCAAGGAGTCTTGGGAGATGAATTCAGAAGAG T A FKBP4P1 Ensembl:ENSG00000251463 Pseudogene exon GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1218633566 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17410015 34405 RMVar_ID_34405 Human_SNP_ID_200704503 A-to-I Human chr4 - 118677566 118677566 118677566 AAGTTAGCTGGGGATGGTGGCGTGTACCTGTTATCCCAGCTACTCGGGAGACTGAGGCAGGAGAA AAGTTAGCTGGGGATGGTGGCGTGTACCTGTTGTCCCAGCTACTCGGGAGACTGAGGCAGGAGAA T C METTL14-DT Ensembl:ENSG00000281731 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1448818061 Functional Loss SNV dbSNP153 33..33 33 - - - 34406 RMVar_ID_34406 Human_SNP_ID_200710481 A-to-I Human chr4 + 118701376 118701376 118701376 CCTGGCTAATTTTTTTAGTATTTGTAGAGATGAGGTCTTGTTATGTTGCCCAGGCTGGCCCCAAA CCTGGCTAATTTTTTTAGTATTTGTAGAGATGCGGTCTTGTTATGTTGCCCAGGCTGGCCCCAAA A C METTL14 Ensembl:ENSG00000145388 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1463118090 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15031050 RMVar_hsa_circ_14180,RMVar_hsa_circ_69273,RMVar_hsa_circ_228229 34407 RMVar_ID_34407 Human_SNP_ID_200712103 A-to-I Human chr4 + 118707990 118707990 118707990 GGGACTGCAGGCGTGTGCCACCACACCTGGCTAATTTTTTGTATTTTTAGTAGAGATGATGTTTC GGGACTGCAGGCGTGTGCCACCACACCTGGCTGATTTTTTGTATTTTTAGTAGAGATGATGTTTC A G METTL14 Ensembl:ENSG00000145388 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1206525206 Functional Loss SNV dbSNP153 33..33 33 - - - 34408 RMVar_ID_34408 Human_SNP_ID_200712131 A-to-I Human chr4 + 118708100 118708100 118708100 GCCCGCCTTGGCCTCCAAATTGCTGGGATTACAAGTGTGAGCCACCACACACCCAAGCCAGACTA GCCCGCCTTGGCCTCCAAATTGCTGGGATTACGAGTGTGAGCCACCACACACCCAAGCCAGACTA A G METTL14 Ensembl:ENSG00000145388 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1349330561 Functional Loss SNV dbSNP153 33..33 33 - - - 34409 RMVar_ID_34409 Human_SNP_ID_200713573 A-to-I Human chr4 + 118714596 118714596 118714596 TAACAAAATACCACATGCATATTTTCTTTTTTATTTTTATTTTTTGAGACAGAGTCTCTGTTACC TAACAAAATACCACATGCATATTTTCTTTTTTCTTTTTATTTTTTGAGACAGAGTCTCTGTTACC A C METTL14 Ensembl:ENSG00000145388 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs755374949 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7261415 34410 RMVar_ID_34410 Human_SNP_ID_200713574 A-to-I Human chr4 + 118714596 118714596 118714596 TAACAAAATACCACATGCATATTTTCTTTTTTATTTTTATTTTTTGAGACAGAGTCTCTGTTACC TAACAAAATACCACATGCATATTTTCTTTTTTGTTTTTATTTTTTGAGACAGAGTCTCTGTTACC A G METTL14 Ensembl:ENSG00000145388 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs755374949 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7261415 34411 RMVar_ID_34411 Human_SNP_ID_200713577 A-to-I Human chr4 + 118714612 118714612 118714612 GCATATTTTCTTTTTTATTTTTATTTTTTGAGACAGAGTCTCTGTTACCCAGGCTGGGGGGCAGT GCATATTTTCTTTTTTATTTTTATTTTTTGAGTCAGAGTCTCTGTTACCCAGGCTGGGGGGCAGT A T METTL14 Ensembl:ENSG00000145388 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs376112255 Functional Loss SNV dbSNP153 33..33 33 - - - 34412 RMVar_ID_34412 Human_SNP_ID_200713617 A-to-I Human chr4 + 118714848 118714848 118714848 ACCTCAACTGATCCACCCACCCTGGCCTCCCAAAGTGTCAGGATTACAGGCGTGAGCCTCTGCAA ACCTCAACTGATCCACCCACCCTGGCCTCCCAGAGTGTCAGGATTACAGGCGTGAGCCTCTGCAA A G METTL14 Ensembl:ENSG00000145388 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971494300 Functional Loss SNV dbSNP153 33..33 33 - - - 34413 RMVar_ID_34413 Human_SNP_ID_200899018 A-to-I Human chr4 + 119502186 119502186 119502186 GAGAACCAAGGAGTAGGAGTGAAACATCTATGATGGATGTTTATCACAGTGCTGTTTGTAATAGT GAGAACCAAGGAGTAGGAGTGAAACATCTATGCTGGATGTTTATCACAGTGCTGTTTGTAATAGT A C AC093752.1 Ensembl:ENSG00000245958 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs945699795 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_306208,RMVar_hsa_circ_335077 34414 RMVar_ID_34414 Human_SNP_ID_200899019 A-to-I Human chr4 + 119502186 119502186 119502186 GAGAACCAAGGAGTAGGAGTGAAACATCTATGATGGATGTTTATCACAGTGCTGTTTGTAATAGT GAGAACCAAGGAGTAGGAGTGAAACATCTATGGTGGATGTTTATCACAGTGCTGTTTGTAATAGT A G AC093752.1 Ensembl:ENSG00000245958 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs945699795 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_306208,RMVar_hsa_circ_335077 34415 RMVar_ID_34415 Human_SNP_ID_200899029 A-to-I Human chr4 - 119502215 119502213 119502215 CGTCCCTTGGTGTAATATTTGCAGTGTTCACTATTACAAACAGCACTGTGATAAACATCCATCAT CGTCCCTTGGTGTAATATTTGCAGTGTTCACT__TACAAACAGCACTGTGATAAACATCCATCAT AAT A PDE5A Ensembl:ENSG00000138735 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1430986983 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_80646,RMVar_hsa_circ_123613,RMVar_hsa_circ_228292,RMVar_hsa_circ_228293,RMVar_hsa_circ_61808,RMVar_hsa_circ_228294 34416 RMVar_ID_34416 Human_SNP_ID_200906683 A-to-I Human chr4 - 119537860 119537860 119537860 CTCTTTTACACAAAACATTATAATTTTTGAATAGTCTATATTCATTTCTTCCACCATTTACTTTT CTCTTTTACACAAAACATTATAATTTTTGAATGGTCTATATTCATTTCTTCCACCATTTACTTTT T C PDE5A Ensembl:ENSG00000138735 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277884366 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_53235,RMVar_hsa_circ_61808,RMVar_hsa_circ_77345,RMVar_hsa_circ_85663,RMVar_hsa_circ_103257,RMVar_hsa_circ_228296,RMVar_hsa_circ_299982,RMVar_hsa_circ_339182,RMVar_hsa_circ_228297,RMVar_hsa_circ_347508,RMVar_hsa_circ_333455,RMVar_hsa_circ_318312,RMVar_hsa_circ_228300,RMVar_hsa_circ_228299,RMVar_hsa_circ_228303,RMVar_hsa_circ_340940,RMVar_hsa_circ_228302,RMVar_hsa_circ_362713,RMVar_hsa_circ_228304 34417 RMVar_ID_34417 Human_SNP_ID_487814156 A-to-I Human chr12 - 15934 15934 15934 GCAGCATGAAGGAGCGAAAGCTGGAGAAGAAGAAGCAGAAGGAGCAGGAGCAAGGTGAGCGGGCC GCAGCATGAAGGAGCGAAAGCTGGAGAAGAAGCAGCAGAAGGAGCAGGAGCAAGGTGAGCGGGCC T G WASH8P Ensembl:ENSG00000226210 Pseudogene exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs797038049 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1319493 34418 RMVar_ID_34418 Human_SNP_ID_487816429 A-to-I Human chr12 - 21162 21162 21162 CCCTTTGGATATTTTGATATTCGAAGGGAATGATCATATTCTCAAAGTCTTCTGATCTTTAGCCA CCCTTTGGATATTTTGATATTCGAAGGGAATGGTCATATTCTCAAAGTCTTCTGATCTTTAGCCA T C WASH8P Ensembl:ENSG00000226210 Pseudogene intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs879949220 Functional Loss SNV dbSNP153 33..33 33 - - - 34419 RMVar_ID_34419 Human_SNP_ID_487911951 A-to-I Human chr12 - 365126 365126 365126 ATTGCTTCAGCCTGGGAGATGGAGGTTGCAGTAAGCTGAGATCCTGCCACTGCACTCCAGCCTGG ATTGCTTCAGCCTGGGAGATGGAGGTTGCAGTGAGCTGAGATCCTGCCACTGCACTCCAGCCTGG T C KDM5A Ensembl:ENSG00000073614 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1347826696 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29544,RMVar_hsa_circ_53342,RMVar_hsa_circ_376519,RMVar_hsa_circ_64329,RMVar_hsa_circ_75829,RMVar_hsa_circ_26255,RMVar_hsa_circ_154157,RMVar_hsa_circ_267489,RMVar_hsa_circ_277767,RMVar_hsa_circ_64135,RMVar_hsa_circ_154163,RMVar_hsa_circ_43473,RMVar_hsa_circ_154166,RMVar_hsa_circ_272410 34420 RMVar_ID_34420 Human_SNP_ID_487916628 A-to-I Human chr12 - 380955 380955 380955 CCTATCTCTACTAATTATGCAAAAAATTAGCCAGGTGTGGTGGTGGGCACCTGTAATTCCATCTG CCTATCTCTACTAATTATGCAAAAAATTAGCCGGGTGTGGTGGTGGGCACCTGTAATTCCATCTG T C KDM5A Ensembl:ENSG00000073614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1039386587 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29544,RMVar_hsa_circ_64329,RMVar_hsa_circ_75829,RMVar_hsa_circ_154157,RMVar_hsa_circ_267489,RMVar_hsa_circ_64135,RMVar_hsa_circ_63870 34421 RMVar_ID_34421 Human_SNP_ID_487916943 A-to-I Human chr12 - 381931 381931 381931 ATGGTGGTGGACTCCTGGAGTCCCAGCTAATCAAGAGGCTGAGGCAGGAGGATTGCTTGAGCCCA ATGGTGGTGGACTCCTGGAGTCCCAGCTAATCGAGAGGCTGAGGCAGGAGGATTGCTTGAGCCCA T C KDM5A Ensembl:ENSG00000073614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs989097044 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29544,RMVar_hsa_circ_64329,RMVar_hsa_circ_75829,RMVar_hsa_circ_154157,RMVar_hsa_circ_267489,RMVar_hsa_circ_64135,RMVar_hsa_circ_63870 34422 RMVar_ID_34422 Human_SNP_ID_487916981 A-to-I Human chr12 - 382086 382086 382086 GAATAATTCGTGGCATGTGGTGGCTCATACCTATAATCCCAGCACTTTGGGAGGCTGAGGTGGAA GAATAATTCGTGGCATGTGGTGGCTCATACCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGAA T C KDM5A Ensembl:ENSG00000073614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs898324773 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29544,RMVar_hsa_circ_64329,RMVar_hsa_circ_75829,RMVar_hsa_circ_154157,RMVar_hsa_circ_267489,RMVar_hsa_circ_64135,RMVar_hsa_circ_63870 34423 RMVar_ID_34423 Human_SNP_ID_487917338 A-to-I Human chr12 - 383339 383339 383339 ATGGTGGTGCACACCTGTAGTCTCAACCACTCAGGAGGCTAAGGTGGGAGGATCACATGAGTCCG ATGGTGGTGCACACCTGTAGTCTCAACCACTCTGGAGGCTAAGGTGGGAGGATCACATGAGTCCG T A KDM5A Ensembl:ENSG00000073614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs914477293 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29544,RMVar_hsa_circ_64329,RMVar_hsa_circ_75829,RMVar_hsa_circ_154157,RMVar_hsa_circ_267489,RMVar_hsa_circ_64135,RMVar_hsa_circ_63870 34424 RMVar_ID_34424 Human_SNP_ID_487923028 A-to-I Human chr12 + 404553 404553 404553 ACTTTGGAAGGCCAAGGGAGGAGGATTGTTTGAGTCCGGGAGTTCAAGGCCAGCCTGGGCAACAT ACTTTGGAAGGCCAAGGGAGGAGGATTGTTTGCGTCCGGGAGTTCAAGGCCAGCCTGGGCAACAT A C CCDC77 Ensembl:ENSG00000120647 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs954062327 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99817,RMVar_hsa_circ_154167 34425 RMVar_ID_34425 Human_SNP_ID_487927785 A-to-I Human chr12 + 418736 418736 418736 TTCATTCATTGATTTAGAGGCAGTATCACTCTATTGCCCAGGCTGGAGTACAGTGGCGCTCTCTT TTCATTCATTGATTTAGAGGCAGTATCACTCTGTTGCCCAGGCTGGAGTACAGTGGCGCTCTCTT A G CCDC77 Ensembl:ENSG00000120647 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1250399639 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_154175,RMVar_hsa_circ_40087,RMVar_hsa_circ_294114,RMVar_hsa_circ_345083,RMVar_hsa_circ_275475,RMVar_hsa_circ_56226,RMVar_hsa_circ_10551,RMVar_hsa_circ_154171,RMVar_hsa_circ_154170,RMVar_hsa_circ_335979,RMVar_hsa_circ_110027,RMVar_hsa_circ_154172,RMVar_hsa_circ_154173,RMVar_hsa_circ_378054,RMVar_hsa_circ_314908,RMVar_hsa_circ_154176,RMVar_hsa_circ_310041 34426 RMVar_ID_34426 Human_SNP_ID_487987846 A-to-I Human chr12 - 641584 641584 641584 TGCCTCGGCCTCCCAGAGTGCTGGCTGGGATTACAAGTGTGAGCCACCGCGCCCGGCCCTAGCCT TGCCTCGGCCTCCCAGAGTGCTGGCTGGGATTGCAAGTGTGAGCCACCGCGCCCGGCCCTAGCCT T C NINJ2 Ensembl:ENSG00000171840 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1051158337 Functional Loss SNV dbSNP153 33..33 33 - - - 34427 RMVar_ID_34427 Human_SNP_ID_488019557 A-to-I Human chr12 + 763328 763328 763328 ATTGTTGGCTAGGCGTGGTGGCTCACGCTTGTAATCCCAACACTTTGGGAGGCCGAGGTTAGTGG ATTGTTGGCTAGGCGTGGTGGCTCACGCTTGTTATCCCAACACTTTGGGAGGCCGAGGTTAGTGG A T WNK1 Ensembl:ENSG00000060237 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1455327345 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12048067 RMVar_hsa_circ_80852,RMVar_hsa_circ_154189 34428 RMVar_ID_34428 Human_SNP_ID_488019569 A-to-I Human chr12 + 763374 763374 763374 GGGAGGCCGAGGTTAGTGGATAACCTGAGGTCAGAAGTTGGAGACCAGCCTAGTCAACATGGTGA GGGAGGCCGAGGTTAGTGGATAACCTGAGGTCGGAAGTTGGAGACCAGCCTAGTCAACATGGTGA A G WNK1 Ensembl:ENSG00000060237 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs887681684 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25006968 RMVar_hsa_circ_80852,RMVar_hsa_circ_154189 34429 RMVar_ID_34429 Human_SNP_ID_488019997 A-to-I Human chr12 + 765091 765091 765091 TCCTCAGGTGATCCACCCATCTCAGTCTTCCAAAGTGCTGGGAGTACAGGTGTGAGCCACTGCGT TCCTCAGGTGATCCACCCATCTCAGTCTTCCAGAGTGCTGGGAGTACAGGTGTGAGCCACTGCGT A G WNK1 Ensembl:ENSG00000060237 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1250982891 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80852,RMVar_hsa_circ_154189 34430 RMVar_ID_34430 Human_SNP_ID_488024356 A-to-I Human chr12 + 782638 782638 782638 GCGATTCTCCTGCCTTGGCCTTCCGAGCAGCTAGGATTACAGGCATGCACCACCACGCCCAGCTA GCGATTCTCCTGCCTTGGCCTTCCGAGCAGCTGGGATTACAGGCATGCACCACCACGCCCAGCTA A G WNK1 Ensembl:ENSG00000060237 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1305157453 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80852,RMVar_hsa_circ_154189 34431 RMVar_ID_34431 Human_SNP_ID_488044786 A-to-I Human chr12 + 866852 866852 866852 GAATCAGAAAATTCATGGTTACGGCCGGGCTCAGTGGCTCACGCCTGTAATCCTAGCACTTTGGG GAATCAGAAAATTCATGGTTACGGCCGGGCTCGGTGGCTCACGCCTGTAATCCTAGCACTTTGGG A G WNK1 Ensembl:ENSG00000060237 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1051729372 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61884,RMVar_hsa_circ_123914,RMVar_hsa_circ_360216,RMVar_hsa_circ_81954,RMVar_hsa_circ_154196,RMVar_hsa_circ_3227,RMVar_hsa_circ_154197,RMVar_hsa_circ_355589 34432 RMVar_ID_34432 Human_SNP_ID_488046262 A-to-I Human chr12 + 872147 872147 872147 ATTTATTTATTTATTTATTTTTATTTATTTTGAGACAGCCTTGCTCTGTTGCCCAGGCTGGAGTG ATTTATTTATTTATTTATTTTTATTTATTTTGGGACAGCCTTGCTCTGTTGCCCAGGCTGGAGTG A G WNK1 Ensembl:ENSG00000060237 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971421336 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6237782,Human_RBP_ID_9709532,Human_RBP_ID_12067294,Human_RBP_ID_25028575 RMVar_hsa_circ_61884,RMVar_hsa_circ_123914,RMVar_hsa_circ_31818,RMVar_hsa_circ_154196,RMVar_hsa_circ_3227,RMVar_hsa_circ_76827,RMVar_hsa_circ_109216,RMVar_hsa_circ_61317,RMVar_hsa_circ_154201,RMVar_hsa_circ_154202 34433 RMVar_ID_34433 Human_SNP_ID_488053393 A-to-I Human chr12 + 898686 898686 898686 GCCTCAAACTCCTAGGCTCAGGTGGTCCTCCTACCTTAGCTTCCTGGGTAGCTGGGATTACAGGC GCCTCAAACTCCTAGGCTCAGGTGGTCCTCCTGCCTTAGCTTCCTGGGTAGCTGGGATTACAGGC A G WNK1 Ensembl:ENSG00000060237 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1474013849 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5205,RMVar_hsa_circ_61884,RMVar_hsa_circ_371180,RMVar_hsa_circ_66595,RMVar_hsa_circ_154207,RMVar_hsa_circ_368991,RMVar_hsa_circ_154216,RMVar_hsa_circ_17778,RMVar_hsa_circ_362986 34434 RMVar_ID_34434 Human_SNP_ID_488053414 A-to-I Human chr12 + 898765 898765 898765 CCTGCTAACTTTGAATTTTTTTTTTGAGACAGAATCCCGCTCTGTTGCCCAGGCTGGAGTGCAGT CCTGCTAACTTTGAATTTTTTTTTTGAGACAGCATCCCGCTCTGTTGCCCAGGCTGGAGTGCAGT A C WNK1 Ensembl:ENSG00000060237 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1419609535 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5205,RMVar_hsa_circ_61884,RMVar_hsa_circ_371180,RMVar_hsa_circ_66595,RMVar_hsa_circ_154207,RMVar_hsa_circ_368991,RMVar_hsa_circ_154216,RMVar_hsa_circ_17778,RMVar_hsa_circ_362986 34435 RMVar_ID_34435 Human_SNP_ID_488053415 A-to-I Human chr12 + 898765 898765 898765 CCTGCTAACTTTGAATTTTTTTTTTGAGACAGAATCCCGCTCTGTTGCCCAGGCTGGAGTGCAGT CCTGCTAACTTTGAATTTTTTTTTTGAGACAGGATCCCGCTCTGTTGCCCAGGCTGGAGTGCAGT A G WNK1 Ensembl:ENSG00000060237 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1419609535 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5205,RMVar_hsa_circ_61884,RMVar_hsa_circ_371180,RMVar_hsa_circ_66595,RMVar_hsa_circ_154207,RMVar_hsa_circ_368991,RMVar_hsa_circ_154216,RMVar_hsa_circ_17778,RMVar_hsa_circ_362986 34436 RMVar_ID_34436 Human_SNP_ID_488057856 A-to-I Human chr12 - 914899 914899 914899 CCCACCTTGGCCTCCCAAAGTGCTGGGGTTACAGGTGTGAGCCACTGTGCCTGGTCAGATTTTAG CCCACCTTGGCCTCCCAAAGTGCTGGGGTTACGGGTGTGAGCCACTGTGCCTGGTCAGATTTTAG T C RAD52 Ensembl:ENSG00000002016 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1445776073 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97715,RMVar_hsa_circ_106759,RMVar_hsa_circ_102303,RMVar_hsa_circ_154222,RMVar_hsa_circ_154224,RMVar_hsa_circ_87664,RMVar_hsa_circ_154223,RMVar_hsa_circ_154221 34437 RMVar_ID_34437 Human_SNP_ID_488060305 A-to-I Human chr12 - 923837 923836 923838 GCCAGGCTGGTCTTGAACTCCTGACCTCAAGTAATCCGCCTGCCTCGGCCTCCGAAAGTTTTGGG GCCAGGCTGGTCTTGAACTCCTGACCTCAAG__ATCCGCCTGCCTCGGCCTCCGAAAGTTTTGGG TTA T RAD52 Ensembl:ENSG00000002016 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1214202440 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_154226,RMVar_hsa_circ_97715,RMVar_hsa_circ_106759,RMVar_hsa_circ_154222,RMVar_hsa_circ_87664,RMVar_hsa_circ_154223,RMVar_hsa_circ_339242,RMVar_hsa_circ_154221,RMVar_hsa_circ_322123,RMVar_hsa_circ_154228,RMVar_hsa_circ_289034,RMVar_hsa_circ_154227 34438 RMVar_ID_34438 Human_SNP_ID_488061416 A-to-I Human chr12 - 927754 927754 927754 TCAAGTGATTCTCCTGCCTCAGTCTCCTGAGTAGCTGGGATTACAGGTGCCCACCACCACACCCG TCAAGTGATTCTCCTGCCTCAGTCTCCTGAGTTGCTGGGATTACAGGTGCCCACCACCACACCCG T A RAD52 Ensembl:ENSG00000002016 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs758223959 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97715,RMVar_hsa_circ_106759,RMVar_hsa_circ_154222,RMVar_hsa_circ_87664,RMVar_hsa_circ_154223,RMVar_hsa_circ_339242,RMVar_hsa_circ_154221,RMVar_hsa_circ_154228,RMVar_hsa_circ_154227,RMVar_hsa_circ_313723,RMVar_hsa_circ_304861,RMVar_hsa_circ_378180,RMVar_hsa_circ_154229 34439 RMVar_ID_34439 Human_SNP_ID_488061427 A-to-I Human chr12 - 927783 927782 927784 CGGCTCACTGCAACCTCTGCCTCCCAGGTTCAAGTGATTCTCCTGCCTCAGTCTCCTGAGTAGCT CGGCTCACTGCAACCTCTGCCTCCCAGGTTC__GTGATTCTCCTGCCTCAGTCTCCTGAGTAGCT CTT C RAD52 Ensembl:ENSG00000002016 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1278646334 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_97715,RMVar_hsa_circ_106759,RMVar_hsa_circ_154222,RMVar_hsa_circ_87664,RMVar_hsa_circ_154223,RMVar_hsa_circ_339242,RMVar_hsa_circ_154221,RMVar_hsa_circ_154228,RMVar_hsa_circ_154227,RMVar_hsa_circ_313723,RMVar_hsa_circ_304861,RMVar_hsa_circ_378180,RMVar_hsa_circ_154229 34440 RMVar_ID_34440 Human_SNP_ID_488061736 A-to-I Human chr12 - 929029 929029 929029 AAAGCCCGTCTCTACTAAAAATACAAAAAATTAGCTGGGCATGGTGGTGTATGCTTGTAGTCCTA AAAGCCCGTCTCTACTAAAAATACAAAAAATTGGCTGGGCATGGTGGTGTATGCTTGTAGTCCTA T C RAD52 Ensembl:ENSG00000002016 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs558216174 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97715,RMVar_hsa_circ_106759,RMVar_hsa_circ_154222,RMVar_hsa_circ_87664,RMVar_hsa_circ_154223,RMVar_hsa_circ_339242,RMVar_hsa_circ_154221,RMVar_hsa_circ_154228,RMVar_hsa_circ_154227,RMVar_hsa_circ_313723,RMVar_hsa_circ_304861,RMVar_hsa_circ_378180,RMVar_hsa_circ_154229 34441 RMVar_ID_34441 Human_SNP_ID_488066918 A-to-I Human chr12 - 948601 948601 948601 CAGGCTGGAGTACAGTGGCGCCGTCTCGGCTCACTGCAACGTCCGCCTCCTGGGTTCAAGCGATT CAGGCTGGAGTACAGTGGCGCCGTCTCGGCTCTCTGCAACGTCCGCCTCCTGGGTTCAAGCGATT T A RAD52 Ensembl:ENSG00000002016 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs944996569 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87664,RMVar_hsa_circ_154221 34442 RMVar_ID_34442 Human_SNP_ID_488071945 A-to-I Human chr12 - 967854 967854 967854 TCGGCTCACTGCAACCTCCCCCTCCTGGGCTCAGGTGATCCTCCCACCCCAGCCTCTCAAATAGC TCGGCTCACTGCAACCTCCCCCTCCTGGGCTCCGGTGATCCTCCCACCCCAGCCTCTCAAATAGC T G RAD52 Ensembl:ENSG00000002016 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1261072362 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87664,RMVar_hsa_circ_154221 34443 RMVar_ID_34443 Human_SNP_ID_488073750 A-to-I Human chr12 - 973606 973606 973606 GGGCATGGTGGCACATGCCTGTAGTCCCAGCTACTCGGGAGGCTGGGGCAGGAGGATCTCTTGAG GGGCATGGTGGCACATGCCTGTAGTCCCAGCTTCTCGGGAGGCTGGGGCAGGAGGATCTCTTGAG T A RAD52 Ensembl:ENSG00000002016 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1238750454 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87664,RMVar_hsa_circ_154221 34444 RMVar_ID_34444 Human_SNP_ID_488075129 A-to-I Human chr12 - 979229 979229 979229 CGCCTTGTTGCCCTGGTTGTTCTTGAACTCCTAAGCTCAGACAGTCCACCCACCTCGGCCTCCCA CGCCTTGTTGCCCTGGTTGTTCTTGAACTCCTGAGCTCAGACAGTCCACCCACCTCGGCCTCCCA T C RAD52,AC004803.1 Ensembl:ENSG00000002016,Ensembl:ENSG00000250132 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1280969726 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5246315 RMVar_hsa_circ_87664,RMVar_hsa_circ_154221 34445 RMVar_ID_34445 Human_SNP_ID_488084477 A-to-I Human chr12 + 1011684 1011684 1011684 GGCTGGGCACAGTGGCTCATGCCTGTAATCCTAGCAGTTTGGAAGGTCAAGTTGGGCGGATCACC GGCTGGGCACAGTGGCTCATGCCTGTAATCCTGGCAGTTTGGAAGGTCAAGTTGGGCGGATCACC A G ERC1 Ensembl:ENSG00000082805 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs772672026 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85810,RMVar_hsa_circ_92073,RMVar_hsa_circ_154233,RMVar_hsa_circ_154234 34446 RMVar_ID_34446 Human_SNP_ID_488122279 A-to-I Human chr12 + 1155187 1155187 1155187 ATATCTACTAAAAATAAAAAAATCTGATGGGCATATTGGTACGTGCCTGTAGTCTCAGCTACTTG ATATCTACTAAAAATAAAAAAATCTGATGGGCGTATTGGTACGTGCCTGTAGTCTCAGCTACTTG A G ERC1 Ensembl:ENSG00000082805 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1261346903 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2312355,Human_RBP_ID_24947425 RMVar_hsa_circ_92073,RMVar_hsa_circ_154233,RMVar_hsa_circ_360114,RMVar_hsa_circ_366027,RMVar_hsa_circ_363760,RMVar_hsa_circ_341490,RMVar_hsa_circ_310476,RMVar_hsa_circ_21731,RMVar_hsa_circ_53620,RMVar_hsa_circ_359278,RMVar_hsa_circ_367777,RMVar_hsa_circ_355693,RMVar_hsa_circ_13451,RMVar_hsa_circ_373716,RMVar_hsa_circ_154241,RMVar_hsa_circ_154244,RMVar_hsa_circ_352302,RMVar_hsa_circ_53789,RMVar_hsa_circ_42167,RMVar_hsa_circ_303710,RMVar_hsa_circ_26497,RMVar_hsa_circ_154245,RMVar_hsa_circ_62468,RMVar_hsa_circ_329155 34447 RMVar_ID_34447 Human_SNP_ID_488151179 A-to-I Human chr12 + 1267639 1267639 1267639 AATTAATTAGCCGGGCATGAGGGGGTATGCCTATATTCCCAGCTACTTGAGGGACTGAGGTGAGA AATTAATTAGCCGGGCATGAGGGGGTATGCCTGTATTCCCAGCTACTTGAGGGACTGAGGTGAGA A G ERC1 Ensembl:ENSG00000082805 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1324750232 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22901929 RMVar_hsa_circ_20106,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_367777,RMVar_hsa_circ_13451,RMVar_hsa_circ_42167,RMVar_hsa_circ_358674,RMVar_hsa_circ_69245,RMVar_hsa_circ_37177,RMVar_hsa_circ_39259,RMVar_hsa_circ_335405,RMVar_hsa_circ_309153,RMVar_hsa_circ_376635,RMVar_hsa_circ_154252,RMVar_hsa_circ_308526,RMVar_hsa_circ_315604,RMVar_hsa_circ_326696,RMVar_hsa_circ_270629,RMVar_hsa_circ_154257,RMVar_hsa_circ_154254,RMVar_hsa_circ_154255,RMVar_hsa_circ_154256 34448 RMVar_ID_34448 Human_SNP_ID_488173561 A-to-I Human chr12 + 1354808 1354808 1354808 AAGTAGCTGAGACTACAGGAGTGCGCCCGGCTAGTTTTTGTGTTTTTGTAGAGACGGGGTGTCAC AAGTAGCTGAGACTACAGGAGTGCGCCCGGCTGGTTTTTGTGTTTTTGTAGAGACGGGGTGTCAC A G ERC1 Ensembl:ENSG00000082805 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973533689 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11890338 RMVar_hsa_circ_20106,RMVar_hsa_circ_92073,RMVar_hsa_circ_154233,RMVar_hsa_circ_363760,RMVar_hsa_circ_341490,RMVar_hsa_circ_21731,RMVar_hsa_circ_13451,RMVar_hsa_circ_42167,RMVar_hsa_circ_69245,RMVar_hsa_circ_39259,RMVar_hsa_circ_376635,RMVar_hsa_circ_308526,RMVar_hsa_circ_315604,RMVar_hsa_circ_326696,RMVar_hsa_circ_154258,RMVar_hsa_circ_271467,RMVar_hsa_circ_276587,RMVar_hsa_circ_293183,RMVar_hsa_circ_312382,RMVar_hsa_circ_154260,RMVar_hsa_circ_154259 34449 RMVar_ID_34449 Human_SNP_ID_488190996 A-to-I Human chr12 + 1418852 1418850 1418852 CTCTTGCCTCAGACACCTGAGTAGCAGGGACTACACGCGTGTACCACCATGCCCTGCTAAATTTT CTCTTGCCTCAGACACCTGAGTAGCAGGGAC__CACGCGTGTACCACCATGCCCTGCTAAATTTT CTA C ERC1 Ensembl:ENSG00000082805 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1271285148 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_92073,RMVar_hsa_circ_154233,RMVar_hsa_circ_363760,RMVar_hsa_circ_69245,RMVar_hsa_circ_39259,RMVar_hsa_circ_326696,RMVar_hsa_circ_154258,RMVar_hsa_circ_293183,RMVar_hsa_circ_154267,RMVar_hsa_circ_283022 34450 RMVar_ID_34450 Human_SNP_ID_488190997 A-to-I Human chr12 + 1418852 1418852 1418852 CTCTTGCCTCAGACACCTGAGTAGCAGGGACTACACGCGTGTACCACCATGCCCTGCTAAATTTT CTCTTGCCTCAGACACCTGAGTAGCAGGGACTGCACGCGTGTACCACCATGCCCTGCTAAATTTT A G ERC1 Ensembl:ENSG00000082805 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs116675483 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92073,RMVar_hsa_circ_154233,RMVar_hsa_circ_363760,RMVar_hsa_circ_69245,RMVar_hsa_circ_39259,RMVar_hsa_circ_326696,RMVar_hsa_circ_154258,RMVar_hsa_circ_293183,RMVar_hsa_circ_154267,RMVar_hsa_circ_283022 34451 RMVar_ID_34451 Human_SNP_ID_488190998 A-to-I Human chr12 + 1418852 1418852 1418852 CTCTTGCCTCAGACACCTGAGTAGCAGGGACTACACGCGTGTACCACCATGCCCTGCTAAATTTT CTCTTGCCTCAGACACCTGAGTAGCAGGGACTTCACGCGTGTACCACCATGCCCTGCTAAATTTT A T ERC1 Ensembl:ENSG00000082805 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs116675483 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92073,RMVar_hsa_circ_154233,RMVar_hsa_circ_363760,RMVar_hsa_circ_69245,RMVar_hsa_circ_39259,RMVar_hsa_circ_326696,RMVar_hsa_circ_154258,RMVar_hsa_circ_293183,RMVar_hsa_circ_154267,RMVar_hsa_circ_283022 34452 RMVar_ID_34452 Human_SNP_ID_488198315 A-to-I Human chr12 + 1445491 1445491 1445491 GACCTCAAGTGATCCTCCCACCTTGGCCTCCCAAGGTGCTGGGATTACAGGCGTGATTCACCGCG GACCTCAAGTGATCCTCCCACCTTGGCCTCCCGAGGTGCTGGGATTACAGGCGTGATTCACCGCG A G ERC1 Ensembl:ENSG00000082805 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1476347401 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92073,RMVar_hsa_circ_154233 34453 RMVar_ID_34453 Human_SNP_ID_488237680 A-to-I Human chr12 - 1592122 1592122 1592122 TTTTTCTGAAGCCCTGGAATTCTACAAGAGAGATATTTTGAGACTGAAACATGTTTGTGCCTAGA TTTTTCTGAAGCCCTGGAATTCTACAAGAGAGGTATTTTGAGACTGAAACATGTTTGTGCCTAGA T C FBXL14 Ensembl:ENSG00000171823 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1429245874 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_991192,Human_RBP_ID_6160549,Human_RBP_ID_11893212,Human_RBP_ID_17353358,Human_RBP_ID_17469972,Human_RBP_ID_18258020,Human_RBP_ID_18623497 34454 RMVar_ID_34454 Human_SNP_ID_488266567 A-to-I Human chr12 + 1698257 1698257 1698257 TGTGTGTGTGTGTGTATTTTATTTAATTTCTGAGACAGGGTCTTGCTCTGTCACCCAGGCTGGAG TGTGTGTGTGTGTGTATTTTATTTAATTTCTGTGACAGGGTCTTGCTCTGTCACCCAGGCTGGAG A T ADIPOR2 Ensembl:ENSG00000006831 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459272227 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2317382,Human_RBP_ID_3400187,Human_RBP_ID_6160709,Human_RBP_ID_11893452 34455 RMVar_ID_34455 Human_SNP_ID_488388283 A-to-I Human chr12 + 2180945 2180945 2180945 CTGGGGACGGGTGCAGCTTGGGATTGTGTTATATTTGTAGCAGTTCTGATGACAACAAGAATAAA CTGGGGACGGGTGCAGCTTGGGATTGTGTTATGTTTGTAGCAGTTCTGATGACAACAAGAATAAA A G CACNA1C Ensembl:ENSG00000151067 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1221269985 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47124,RMVar_hsa_circ_368715,RMVar_hsa_circ_43485 34456 RMVar_ID_34456 Human_SNP_ID_488388299 A-to-I Human chr12 + 2181023 2181023 2181023 ATTTGTTTCATGAACATAACCCTCAAATCTGCACTCCCCTATTACGTGTTTGGGCAACTGAGTTT ATTTGTTTCATGAACATAACCCTCAAATCTGCTCTCCCCTATTACGTGTTTGGGCAACTGAGTTT A T CACNA1C Ensembl:ENSG00000151067 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1455781325 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47124,RMVar_hsa_circ_368715,RMVar_hsa_circ_43485 34457 RMVar_ID_34457 Human_SNP_ID_488388443 A-to-I Human chr12 + 2181722 2181722 2181722 CAGGGGACCCACATCCACGATATCGTTTTTTTACAGCTCATTACTGAATCCTCACAATAACCCCA CAGGGGACCCACATCCACGATATCGTTTTTTTGCAGCTCATTACTGAATCCTCACAATAACCCCA A G CACNA1C Ensembl:ENSG00000151067 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1395501416 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47124,RMVar_hsa_circ_368715,RMVar_hsa_circ_43485 34458 RMVar_ID_34458 Human_SNP_ID_488532127 A-to-I Human chr12 - 2749758 2749758 2749758 AAACTAAGAACGCTGAAAAAAGGTTAGAGGATACCCCTCCCCCACCAAGCTCAAGCATCCCAGGT AAACTAAGAACGCTGAAAAAAGGTTAGAGGATGCCCCTCCCCCACCAAGCTCAAGCATCCCAGGT T C ITFG2-AS1 Ensembl:ENSG00000256150 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1452337853 Functional Loss SNV dbSNP153 33..33 33 - - - 34459 RMVar_ID_34459 Human_SNP_ID_488547737 A-to-I Human chr12 - 2808259 2808259 2808259 GCGCTCTTGACTCACTGCAAGCTCCACCTCCCAGGTTCACACCATTCTCCTGCCTCAGCCTCCCC GCGCTCTTGACTCACTGCAAGCTCCACCTCCCGGGTTCACACCATTCTCCTGCCTCAGCCTCCCC T C ITFG2-AS1,ITFG2-AS1:2 Ensembl:ENSG00000256150,Ensembl:ENSG00000258325 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1362595627 Functional Loss SNV dbSNP153 33..33 33 - - - 34460 RMVar_ID_34460 Human_SNP_ID_488552904 A-to-I Human chr12 + 2825840 2825840 2825840 GCTGGAGTCCGATGGCACGAACTTGGCTCACTACAACCCCCATCTCCCAGGTTCAAGCAACTCCT GCTGGAGTCCGATGGCACGAACTTGGCTCACTGCAACCCCCATCTCCCAGGTTCAAGCAACTCCT A G ITFG2 Ensembl:ENSG00000111203 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985204452 Functional Loss SNV dbSNP153 33..33 33 - - - 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 34461 RMVar_ID_34461 Human_SNP_ID_488552906 A-to-I Human chr12 + 2825842 2825842 2825842 TGGAGTCCGATGGCACGAACTTGGCTCACTACAACCCCCATCTCCCAGGTTCAAGCAACTCCTAT TGGAGTCCGATGGCACGAACTTGGCTCACTACCACCCCCATCTCCCAGGTTCAAGCAACTCCTAT A C ITFG2 Ensembl:ENSG00000111203 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs926621773 Functional Loss SNV dbSNP153 33..33 33 - - - 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 34462 RMVar_ID_34462 Human_SNP_ID_488552907 A-to-I Human chr12 + 2825842 2825842 2825842 TGGAGTCCGATGGCACGAACTTGGCTCACTACAACCCCCATCTCCCAGGTTCAAGCAACTCCTAT TGGAGTCCGATGGCACGAACTTGGCTCACTACGACCCCCATCTCCCAGGTTCAAGCAACTCCTAT A G ITFG2 Ensembl:ENSG00000111203 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs926621773 Functional Loss SNV dbSNP153 33..33 33 - - - 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 34463 RMVar_ID_34463 Human_SNP_ID_488554027 A-to-I Human chr12 + 2829692 2829692 2829692 AGAAGACTGAGGTGGGAGGATCGCTTGAGTCCAGGAGGTTGAGGCTGCAATGAGCTCTGATCATG AGAAGACTGAGGTGGGAGGATCGCTTGAGTCCTGGAGGTTGAGGCTGCAATGAGCTCTGATCATG A T ITFG2 Ensembl:ENSG00000111203 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037617475 Functional Loss SNV dbSNP153 33..33 33 - - - 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 34464 RMVar_ID_34464 Human_SNP_ID_488554030 A-to-I Human chr12 + 2829708 2829708 2829708 AGGATCGCTTGAGTCCAGGAGGTTGAGGCTGCAATGAGCTCTGATCATGCCACTACACTCCAGCC AGGATCGCTTGAGTCCAGGAGGTTGAGGCTGCCATGAGCTCTGATCATGCCACTACACTCCAGCC A C ITFG2 Ensembl:ENSG00000111203 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1337696533 Functional Loss SNV dbSNP153 33..33 33 - - - 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 34465 RMVar_ID_34465 Human_SNP_ID_488556871 A-to-I Human chr12 + 2839230 2839230 2839230 GGGGAATCACTTGAACCTGAAAGGCAGAGGTTACAGTGAGCCGAGATCATGCCACTGCACTCCAG GGGGAATCACTTGAACCTGAAAGGCAGAGGTTGCAGTGAGCCGAGATCATGCCACTGCACTCCAG A G ITFG2 Ensembl:ENSG00000111203 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs767497398 Functional Loss SNV dbSNP153 33..33 33 - - - 34466 RMVar_ID_34466 Human_SNP_ID_488558319 A-to-I Human chr12 + 2844433 2844433 2844433 AAAATTAGCTGAGCATAGCGGTGTGCGCTTGTAATCCCAGCTACTTGGGAAGCTGAGACAGGAGA AAAATTAGCTGAGCATAGCGGTGTGCGCTTGTGATCCCAGCTACTTGGGAAGCTGAGACAGGAGA A G ITFG2 Ensembl:ENSG00000111203 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1441780822 Functional Loss SNV dbSNP153 33..33 33 - - - 34467 RMVar_ID_34467 Human_SNP_ID_488560192 A-to-I Human chr12 + 2851395 2851395 2851395 ATGGAGTCTGACTCTGTCCCTGATGCTCGAGCACAGTGGCCATGATCTTGGCTCACTGCAACCTC ATGGAGTCTGACTCTGTCCCTGATGCTCGAGCGCAGTGGCCATGATCTTGGCTCACTGCAACCTC A G ITFG2 Ensembl:ENSG00000111203 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs572599799 Functional Loss SNV dbSNP153 33..33 33 - - - 34468 RMVar_ID_34468 Human_SNP_ID_488560488 A-to-I Human chr12 + 2852506 2852506 2852506 CTCCCACTTCAGCCTCCCATGTAGCTGGGATTATGGGCATGTGCCACCATGCCTGGCTAATTTTT CTCCCACTTCAGCCTCCCATGTAGCTGGGATTGTGGGCATGTGCCACCATGCCTGGCTAATTTTT A G ITFG2 Ensembl:ENSG00000111203 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1186634125 Functional Loss SNV dbSNP153 33..33 33 - - - 34469 RMVar_ID_34469 Human_SNP_ID_488561004 A-to-I Human chr12 + 2854081 2854081 2854081 GAGTTTCTCTCTTGTTGCCCCGGCTGGAGTGCAATGGCACCATCTTGGCTCACTGCAACCTCCGC GAGTTTCTCTCTTGTTGCCCCGGCTGGAGTGCGATGGCACCATCTTGGCTCACTGCAACCTCCGC A G ITFG2 Ensembl:ENSG00000111203 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335413671 Functional Loss SNV dbSNP153 33..33 33 - - - 34470 RMVar_ID_34470 Human_SNP_ID_488565576 A-to-I Human chr12 - 2869611 2869611 2869611 CCAATATGGTAAACCCCATCTCTACTAAAAATACAAAAAAAGTAGCTGGGCGTGGTGGCAGGCAC CCAATATGGTAAACCCCATCTCTACTAAAAATGCAAAAAAAGTAGCTGGGCGTGGTGGCAGGCAC T C FOXM1 Ensembl:ENSG00000111206 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1035865898 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24962770 RMVar_hsa_circ_91591,RMVar_hsa_circ_154335,RMVar_hsa_circ_369612,RMVar_hsa_circ_154341,RMVar_hsa_circ_98493,RMVar_hsa_circ_100125,RMVar_hsa_circ_154343,RMVar_hsa_circ_154346,RMVar_hsa_circ_335015 34471 RMVar_ID_34471 Human_SNP_ID_488565583 A-to-I Human chr12 - 2869640 2869640 2869640 CTGAGGTCAGGAGTTCGAGACTAGCCTGGCCAATATGGTAAACCCCATCTCTACTAAAAATACAA CTGAGGTCAGGAGTTCGAGACTAGCCTGGCCAGTATGGTAAACCCCATCTCTACTAAAAATACAA T C FOXM1 Ensembl:ENSG00000111206 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs749801267 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91591,RMVar_hsa_circ_154335,RMVar_hsa_circ_369612,RMVar_hsa_circ_154341,RMVar_hsa_circ_98493,RMVar_hsa_circ_100125,RMVar_hsa_circ_154343,RMVar_hsa_circ_154346,RMVar_hsa_circ_335015 34472 RMVar_ID_34472 Human_SNP_ID_488567938 A-to-I Human chr12 + 2877961 2877961 2877961 CCAGCACTTTAGGAGGCCGAGGCGGGTGGATCACTTGAGGTCACGAGTTCGAGACCAGCCTGGCA CCAGCACTTTAGGAGGCCGAGGCGGGTGGATCTCTTGAGGTCACGAGTTCGAGACCAGCCTGGCA A T RHNO1,TULP3 Ensembl:ENSG00000171792,Ensembl:ENSG00000078246 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1163426054 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1325122 RMVar_hsa_circ_127855,RMVar_hsa_circ_154349 34473 RMVar_ID_34473 Human_SNP_ID_488567987 A-to-I Human chr12 + 2878087 2878087 2878087 CCAGCTACTCTGGAGGCTGAGGTGGAAGGATCACCTGAGGCCGAGAGGTGGAGGCTATGGTAAGC CCAGCTACTCTGGAGGCTGAGGTGGAAGGATCCCCTGAGGCCGAGAGGTGGAGGCTATGGTAAGC A C RHNO1,TULP3 Ensembl:ENSG00000171792,Ensembl:ENSG00000078246 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1448408974 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1325123 RMVar_hsa_circ_127855,RMVar_hsa_circ_154349 34474 RMVar_ID_34474 Human_SNP_ID_488568001 A-to-I Human chr12 + 2878154 2878153 2878155 TGATCACACCACTGCACTCCAGCCTGGGCGACAGAGGGAGACACCGTCTCCAAAACAAACAAATG TGATCACACCACTGCACTCCAGCCTGGGCGAC__AGGGAGACACCGTCTCCAAAACAAACAAATG CAG C RHNO1,TULP3 Ensembl:ENSG00000171792,Ensembl:ENSG00000078246 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs888972814 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_127855,RMVar_hsa_circ_154349 34475 RMVar_ID_34475 Human_SNP_ID_488568226 A-to-I Human chr12 + 2879099 2879099 2879099 TTGGCTCACTACAACCTCAACCTCCTGGGCTCAGGTGATCCTCCCACCTCAGCCTCCTGAATGGC TTGGCTCACTACAACCTCAACCTCCTGGGCTCCGGTGATCCTCCCACCTCAGCCTCCTGAATGGC A C RHNO1,TULP3 Ensembl:ENSG00000171792,Ensembl:ENSG00000078246 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs578035230 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127855,RMVar_hsa_circ_154349 34476 RMVar_ID_34476 Human_SNP_ID_488568555 A-to-I Human chr12 + 2880446 2880446 2880446 CAAGACCAGTCTGGCCAACGTGGTGAAACCCCATCTCTACTAAAAAATACTATAATTAGCTGGGC CAAGACCAGTCTGGCCAACGTGGTGAAACCCCCTCTCTACTAAAAAATACTATAATTAGCTGGGC A C RHNO1,TULP3 Ensembl:ENSG00000171792,Ensembl:ENSG00000078246 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1271968308 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17817053 RMVar_hsa_circ_127855,RMVar_hsa_circ_154349 34477 RMVar_ID_34477 Human_SNP_ID_488568636 A-to-I Human chr12 + 2880822 2880821 2880823 TGCCAAGCTAATTATTCTTTTAAATTTGTAGTAGAGACGAGGTCTCTCTATGTTGCCCAGGCTGG TGCCAAGCTAATTATTCTTTTAAATTTGTAGT__AGACGAGGTCTCTCTATGTTGCCCAGGCTGG TAG T RHNO1,TULP3 Ensembl:ENSG00000171792,Ensembl:ENSG00000078246 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1379256387 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_127855,RMVar_hsa_circ_154349 34478 RMVar_ID_34478 Human_SNP_ID_488568743 A-to-I Human chr12 + 2881341 2881341 2881341 GGCAGGCTGGTCTTGAACTCCTGACTTCAAGTAATCTGCCCGCCTCAGCTCCCTAAACTGCTGGT GGCAGGCTGGTCTTGAACTCCTGACTTCAAGTGATCTGCCCGCCTCAGCTCCCTAAACTGCTGGT A G RHNO1,TULP3 Ensembl:ENSG00000171792,Ensembl:ENSG00000078246 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs781640283 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_113278 RMVar_hsa_circ_127855,RMVar_hsa_circ_154349 34479 RMVar_ID_34479 Human_SNP_ID_488568857 A-to-I Human chr12 + 2881854 2881854 2881854 TTGAACCCAGGAGGTAGAGGTTGTGGTGAGCCAAGATCGCGCCACTGTACTCTAGCCTGCGTAAC TTGAACCCAGGAGGTAGAGGTTGTGGTGAGCCTAGATCGCGCCACTGTACTCTAGCCTGCGTAAC A T RHNO1,TULP3 Ensembl:ENSG00000171792,Ensembl:ENSG00000078246 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1295997916 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127855,RMVar_hsa_circ_154349 34480 RMVar_ID_34480 Human_SNP_ID_488569136 A-to-I Human chr12 + 2882963 2882962 2882963 AGTGTGCTTGCTTGTAGTTCCAGCTACTCAGGAAGCTGATGTGGGAGGATTGCTTGGGCTTTAGA AGTGTGCTTGCTTGTAGTTCCAGCTACTCAGG_AGCTGATGTGGGAGGATTGCTTGGGCTTTAGA GA G RHNO1,TULP3 Ensembl:ENSG00000171792,Ensembl:ENSG00000078246 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1425940289 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_23555614 RMVar_hsa_circ_127855,RMVar_hsa_circ_154349 34481 RMVar_ID_34481 Human_SNP_ID_488569151 A-to-I Human chr12 + 2883022 2883022 2883022 TTTAGAGGTTGAGGCTGCAATGATCCATGATCACACCACTGCACTCCAGCCTAGGTGACAGAGCA TTTAGAGGTTGAGGCTGCAATGATCCATGATCGCACCACTGCACTCCAGCCTAGGTGACAGAGCA A G RHNO1,TULP3 Ensembl:ENSG00000171792,Ensembl:ENSG00000078246 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs375533966 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24962970 RMVar_hsa_circ_127855,RMVar_hsa_circ_154349 34482 RMVar_ID_34482 Human_SNP_ID_488569249 A-to-I Human chr12 + 2883123 2883123 2883123 AGAAAACCTGGGGTGTGGTGGCTCACACCTGTAATTCCAGCACTTTGGGAGGCTGAGGTGCGCAG AGAAAACCTGGGGTGTGGTGGCTCACACCTGTGATTCCAGCACTTTGGGAGGCTGAGGTGCGCAG A G RHNO1,TULP3 Ensembl:ENSG00000171792,Ensembl:ENSG00000078246 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1413979400 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23555615 RMVar_hsa_circ_127855,RMVar_hsa_circ_154349 34483 RMVar_ID_34483 Human_SNP_ID_488569270 A-to-I Human chr12 + 2883208 2883208 2883208 CAAGACTAGCCTGGGCAATACAACGAAACCCTATTTCTACAAAAATACGAAAATTAGCCAGCGCT CAAGACTAGCCTGGGCAATACAACGAAACCCTGTTTCTACAAAAATACGAAAATTAGCCAGCGCT A G RHNO1,TULP3 Ensembl:ENSG00000171792,Ensembl:ENSG00000078246 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs917152412 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127855,RMVar_hsa_circ_154349 34484 RMVar_ID_34484 Human_SNP_ID_488570455 A-to-I Human chr12 + 2886464 2886464 2886464 CTTGAGCCCAGGAGTTCGAGACCAGCCTGGGCAACATGGTGAAACCCCATCTTTACTAAAAATAT CTTGAGCCCAGGAGTTCGAGACCAGCCTGGGCCACATGGTGAAACCCCATCTTTACTAAAAATAT A C RHNO1,TULP3 Ensembl:ENSG00000171792,Ensembl:ENSG00000078246 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1020790208 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127855,RMVar_hsa_circ_154349 34485 RMVar_ID_34485 Human_SNP_ID_488570477 A-to-I Human chr12 + 2886558 2886558 2886558 GCGCACCTGTAGTCCCAGCTACTTGGGAGGCTAAGGTGGGCAGATCTCTTGAACCGGGAGGTCAA GCGCACCTGTAGTCCCAGCTACTTGGGAGGCTCAGGTGGGCAGATCTCTTGAACCGGGAGGTCAA A C RHNO1,TULP3 Ensembl:ENSG00000171792,Ensembl:ENSG00000078246 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs927897119 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127855,RMVar_hsa_circ_154349 34486 RMVar_ID_34486 Human_SNP_ID_488571124 A-to-I Human chr12 + 2888673 2888673 2888673 CCTCAGCCTCCCCAGTAGCTGGGATTACAGGCACCAGCCACCATGCCTGGCTAATTTTTTTGTAT CCTCAGCCTCCCCAGTAGCTGGGATTACAGGCCCCAGCCACCATGCCTGGCTAATTTTTTTGTAT A C RHNO1,TULP3 Ensembl:ENSG00000171792,Ensembl:ENSG00000078246 Protein coding,Protein coding 3'UTR,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1392555804 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_271405,Human_miRNA_ID_2051829,Human_miRNA_ID_2493310 RMVar_hsa_circ_127855,RMVar_hsa_circ_154349 34487 RMVar_ID_34487 Human_SNP_ID_488571142 A-to-I Human chr12 + 2888713 2888713 2888713 CCATGCCTGGCTAATTTTTTTGTATTTTTAGTAGAGATGTGGTTTCTCCATGTTGGCCAGGCTGG CCATGCCTGGCTAATTTTTTTGTATTTTTAGTGGAGATGTGGTTTCTCCATGTTGGCCAGGCTGG A G RHNO1,TULP3 Ensembl:ENSG00000171792,Ensembl:ENSG00000078246 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs933490746 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9015923 RMVar_hsa_circ_127855,RMVar_hsa_circ_154349 34488 RMVar_ID_34488 Human_SNP_ID_488574193 A-to-I Human chr12 + 2898819 2898819 2898819 CTCCTTCCTCTGCCTCCTGAGTAGCTGGGATTACAGGTGTGCACCACCACACCTGGCTAATTTTT CTCCTTCCTCTGCCTCCTGAGTAGCTGGGATTGCAGGTGTGCACCACCACACCTGGCTAATTTTT A G TULP3 Ensembl:ENSG00000078246 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs918044040 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127855,RMVar_hsa_circ_154349 34489 RMVar_ID_34489 Human_SNP_ID_488575991 A-to-I Human chr12 + 2904909 2904909 2904909 TCATCTTTACCTGAAGTCAGGAGTTTGAGACGAACCTGGCCAACATGGCGAAACCCCGTCTCCAC TCATCTTTACCTGAAGTCAGGAGTTTGAGACGCACCTGGCCAACATGGCGAAACCCCGTCTCCAC A C TULP3 Ensembl:ENSG00000078246 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1471869842 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127855,RMVar_hsa_circ_154349 34490 RMVar_ID_34490 Human_SNP_ID_488583453 A-to-I Human chr12 + 2932350 2932350 2932350 CGTATGATCCCAGCACTTCGGGAGGCTGAGGCAGGTGGATCCCTTGAGGACATGAGCTCGAGACC CGTATGATCCCAGCACTTCGGGAGGCTGAGGCTGGTGGATCCCTTGAGGACATGAGCTCGAGACC A T TULP3 Ensembl:ENSG00000078246 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs746382432 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_154351,RMVar_hsa_circ_351101,RMVar_hsa_circ_118065,RMVar_hsa_circ_368291,RMVar_hsa_circ_3949,RMVar_hsa_circ_269124,RMVar_hsa_circ_328393 34491 RMVar_ID_34491 Human_SNP_ID_488583542 A-to-I Human chr12 + 2932763 2932763 2932763 GCCTTGAACTCCTGGACTCCAGTGATCCCTCTACCTCAGCCTCCCAAGCAGCTGGGATTATAGGC GCCTTGAACTCCTGGACTCCAGTGATCCCTCTGCCTCAGCCTCCCAAGCAGCTGGGATTATAGGC A G TULP3 Ensembl:ENSG00000078246 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1299922407 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_154351,RMVar_hsa_circ_351101,RMVar_hsa_circ_118065,RMVar_hsa_circ_368291,RMVar_hsa_circ_3949,RMVar_hsa_circ_269124,RMVar_hsa_circ_328393 34492 RMVar_ID_34492 Human_SNP_ID_488584833 A-to-I Human chr12 + 2937406 2937406 2937406 GCCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTCAA GCCTGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGGTCTCAA A G TULP3 Ensembl:ENSG00000078246 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs577263146 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_154351,RMVar_hsa_circ_118065,RMVar_hsa_circ_9094,RMVar_hsa_circ_269124,RMVar_hsa_circ_282374,RMVar_hsa_circ_35368,RMVar_hsa_circ_154356 34493 RMVar_ID_34493 Human_SNP_ID_488584834 A-to-I Human chr12 + 2937406 2937406 2937406 GCCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTCAA GCCTGGCTAATTTTTGTATTTTTAGTAGAGACTGGGTTTCACCATGTTGGCCAGGCTGGTCTCAA A T TULP3 Ensembl:ENSG00000078246 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs577263146 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_154351,RMVar_hsa_circ_118065,RMVar_hsa_circ_9094,RMVar_hsa_circ_269124,RMVar_hsa_circ_282374,RMVar_hsa_circ_35368,RMVar_hsa_circ_154356 34494 RMVar_ID_34494 Human_SNP_ID_488584840 A-to-I Human chr12 + 2937417 2937417 2937417 TTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTCCTGACCT TTTTGTATTTTTAGTAGAGACAGGGTTTCACCGTGTTGGCCAGGCTGGTCTCAAACTCCTGACCT A G TULP3 Ensembl:ENSG00000078246 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs904536359 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_154351,RMVar_hsa_circ_118065,RMVar_hsa_circ_9094,RMVar_hsa_circ_269124,RMVar_hsa_circ_282374,RMVar_hsa_circ_35368,RMVar_hsa_circ_154356 34495 RMVar_ID_34495 Human_SNP_ID_488600145 A-to-I Human chr12 + 2990536 2990536 2990536 TTGCCTAGGCTGGAGTGCAGTGGCGTGATCTCAGCTCACTGCAACTCTGCCTCCCAGGTACAAGT TTGCCTAGGCTGGAGTGCAGTGGCGTGATCTCGGCTCACTGCAACTCTGCCTCCCAGGTACAAGT A G TEAD4 Ensembl:ENSG00000197905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1487004756 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11922333 34496 RMVar_ID_34496 Human_SNP_ID_488600239 A-to-I Human chr12 + 2990983 2990983 2990983 AAGGAGGGAGAATTGCTTGAGGCTGGAAGTTCAAGACCAGCCTAGGCAACCTAGTGAGACCTCTG AAGGAGGGAGAATTGCTTGAGGCTGGAAGTTCCAGACCAGCCTAGGCAACCTAGTGAGACCTCTG A C TEAD4 Ensembl:ENSG00000197905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1408114680 Functional Loss SNV dbSNP153 33..33 33 - - - 34497 RMVar_ID_34497 Human_SNP_ID_488606939 A-to-I Human chr12 + 3016262 3016262 3016262 GTTGCCCAGGCTGGCCTAGAACTCCTGGGCTCAAGCGATCTACCAACCTCAGCCTCTCCAGGAGC GTTGCCCAGGCTGGCCTAGAACTCCTGGGCTCGAGCGATCTACCAACCTCAGCCTCTCCAGGAGC A G TEAD4 Ensembl:ENSG00000197905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404690957 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63309,RMVar_hsa_circ_324313,RMVar_hsa_circ_154357,RMVar_hsa_circ_270451,RMVar_hsa_circ_154359 34498 RMVar_ID_34498 Human_SNP_ID_488662377 A-to-I Human chr12 + 3219968 3219968 3219968 CCTGAGGTCAGGAGTTCGAGACTAGCCTGGCCAACGTGGTGAAACCCTGTCTCTACTAAAAATAC CCTGAGGTCAGGAGTTCGAGACTAGCCTGGCCTACGTGGTGAAACCCTGTCTCTACTAAAAATAC A T TSPAN9 Ensembl:ENSG00000011105 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs972207402 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9095 34499 RMVar_ID_34499 Human_SNP_ID_488662392 A-to-I Human chr12 + 3220024 3220024 3220024 TAAAAATACAAAAAGTAGTGGCGCATGCTTGTAGTCCCAGCTGCTTGGAAGGCTAAGGCAGGAGA TAAAAATACAAAAAGTAGTGGCGCATGCTTGTGGTCCCAGCTGCTTGGAAGGCTAAGGCAGGAGA A G TSPAN9 Ensembl:ENSG00000011105 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1473255475 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9095 34500 RMVar_ID_34500 Human_SNP_ID_488813626 A-to-I Human chr12 - 3839945 3839945 3839945 AAGGTTTAAATCCATTCACATCAGCAGCAGCAACAGCAGTTTTACTCTTGCAGCTGTCATCCTCT AAGGTTTAAATCCATTCACATCAGCAGCAGCAGCAGCAGTTTTACTCTTGCAGCTGTCATCCTCT T C PARP11 Ensembl:ENSG00000111224 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs990396986 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_154373,RMVar_hsa_circ_154375,RMVar_hsa_circ_154377,RMVar_hsa_circ_285659,RMVar_hsa_circ_154379,RMVar_hsa_circ_307799,RMVar_hsa_circ_154380 34501 RMVar_ID_34501 Human_SNP_ID_488817777 A-to-I Human chr12 - 3858833 3858833 3858833 CACACACCTGGGCCTCCCAGGGTGCTGGGATTACAGGCGTGAGCCACCGCACCCAGCCTGAATAT CACACACCTGGGCCTCCCAGGGTGCTGGGATTGCAGGCGTGAGCCACCGCACCCAGCCTGAATAT T C PARP11 Ensembl:ENSG00000111224 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1303511747 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_154373,RMVar_hsa_circ_154375,RMVar_hsa_circ_154377,RMVar_hsa_circ_285659,RMVar_hsa_circ_154379,RMVar_hsa_circ_307799,RMVar_hsa_circ_154380 34502 RMVar_ID_34502 Human_SNP_ID_488934160 A-to-I Human chr12 + 4335475 4335475 4335475 ACATTAGGAGGTGGGGTCTTTGGGTGGTTATTAGGTCACAAGGGTGCAGCCCTCATGAATGGAAT ACATTAGGAGGTGGGGTCTTTGGGTGGTTATTTGGTCACAAGGGTGCAGCCCTCATGAATGGAAT A T TIGAR,AC008012.1 Ensembl:ENSG00000078237,Ensembl:ENSG00000285901 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1372299156 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_154393,RMVar_hsa_circ_117086,RMVar_hsa_circ_154392 34503 RMVar_ID_34503 Human_SNP_ID_488938878 A-to-I Human chr12 + 4353671 4353671 4353671 AGCCTGGCCAACAATGGTGAAACCCTGTCTCTACTACAAATACAAAAAAGCCAGGCGTGGTAGCA AGCCTGGCCAACAATGGTGAAACCCTGTCTCTGCTACAAATACAAAAAAGCCAGGCGTGGTAGCA A G TIGAR,AC008012.1 Ensembl:ENSG00000078237,Ensembl:ENSG00000285901 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1321558918 Functional Loss SNV dbSNP153 33..33 33 - - - 34504 RMVar_ID_34504 Human_SNP_ID_488940120 A-to-I Human chr12 + 4357983 4357983 4357983 AAAATTAGCCAGGCCTGGTGGCCGGCGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGTAGA AAAATTAGCCAGGCCTGGTGGCCGGCGCCTGTGGTCCCAGCTACTTGGGAGGCTGAGGCAGTAGA A G TIGAR,AC008012.1 Ensembl:ENSG00000078237,Ensembl:ENSG00000285901 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1316383155 Functional Loss SNV dbSNP153 33..33 33 - - - 34505 RMVar_ID_34505 Human_SNP_ID_488971205 A-to-I Human chr12 - 4488607 4488607 4488607 ATAGAAACTGTTGGCAAGCAGAGTGCTTTCCTATAACAGAATGTGTCTTAATTTTCTACTCGAGG ATAGAAACTGTTGGCAAGCAGAGTGCTTTCCTGTAACAGAATGTGTCTTAATTTTCTACTCGAGG T C C12orf4 Ensembl:ENSG00000047621 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs980633563 Functional Loss SNV dbSNP153 33..33 33 - - - 34506 RMVar_ID_34506 Human_SNP_ID_488990058 A-to-I Human chr12 + 4569661 4569661 4569661 AAAAAATTTGAAAGTAGAGACAGGGTCTCGCTATGTTGCCCAGGCTGGTCTCAAACTCCTGGGCT AAAAAATTTGAAAGTAGAGACAGGGTCTCGCTGTGTTGCCCAGGCTGGTCTCAAACTCCTGGGCT A G DYRK4 Ensembl:ENSG00000010219 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1193639593 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_65281,RMVar_hsa_circ_364808 34507 RMVar_ID_34507 Human_SNP_ID_489388750 A-to-I Human chr12 + 6176391 6176391 6176391 TCACACTTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGAGGATTGAGCCCAGGAGTTCAAGAC TCACACTTGTAATCCCAGCACTTTGGGAGGCCCAGGCGGGAGGATTGAGCCCAGGAGTTCAAGAC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017044499 Functional Loss SNV dbSNP153 33..33 33 - - - 34508 RMVar_ID_34508 Human_SNP_ID_489388751 A-to-I Human chr12 + 6176391 6176391 6176391 TCACACTTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGAGGATTGAGCCCAGGAGTTCAAGAC TCACACTTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGAGGATTGAGCCCAGGAGTTCAAGAC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017044499 Functional Loss SNV dbSNP153 33..33 33 - - - 34509 RMVar_ID_34509 Human_SNP_ID_489414664 A-to-I Human chr12 - 6270305 6270305 6270305 GCCCTAGTGGCATTTTCGGAGCATTTCGAAGAAGTTACTACCGGTACTACAACAAGTACATCAAT GCCCTAGTGGCATTTTCGGAGCATTTCGAAGAGGTTACTACCGGTACTACAACAAGTACATCAAT T C ATP5MFP5 Ensembl:ENSG00000256103 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879197163 Functional Loss SNV dbSNP153 33..33 33 - - - 34510 RMVar_ID_34510 Human_SNP_ID_489414668 A-to-I Human chr12 - 6270315 6270315 6270315 CGGGACTTCAGCCCTAGTGGCATTTTCGGAGCATTTCGAAGAAGTTACTACCGGTACTACAACAA CGGGACTTCAGCCCTAGTGGCATTTTCGGAGCGTTTCGAAGAAGTTACTACCGGTACTACAACAA T C ATP5MFP5 Ensembl:ENSG00000256103 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879079189 Functional Loss SNV dbSNP153 33..33 33 - - - 34511 RMVar_ID_34511 Human_SNP_ID_489428694 A-to-I Human chr12 - 6321112 6321112 6321112 GGGAGGCTAAGCTGGGAGACTCACTTGAGCCCAGGAAGTTGAGGCGGCAGTGAGCTGTGATCATG GGGAGGCTAAGCTGGGAGACTCACTTGAGCCCGGGAAGTTGAGGCGGCAGTGAGCTGTGATCATG T C lnc-TNFRSF1A-3 RNACentral:URS00008BB61A lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1397549186 Functional Loss SNV dbSNP153 33..33 33 - - - 34512 RMVar_ID_34512 Human_SNP_ID_489439362 A-to-I Human chr12 - 6357339 6357339 6357339 AAACTTCTGACTTCAACTGATCCACCTGTCTCAGCCTCCCAAAGTGTTGGGATTACAGGCGTGAG AAACTTCTGACTTCAACTGATCCACCTGTCTCGGCCTCCCAAAGTGTTGGGATTACAGGCGTGAG T C SCNN1A Ensembl:ENSG00000111319 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs545588475 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_698,RMVar_hsa_circ_91849,RMVar_hsa_circ_154488,RMVar_hsa_circ_119541,RMVar_hsa_circ_100555,RMVar_hsa_circ_154493,RMVar_hsa_circ_154494 34513 RMVar_ID_34513 Human_SNP_ID_489439368 A-to-I Human chr12 - 6357394 6357394 6357394 AATTTTTGTATTTTTGGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTTCTGA AATTTTTGTATTTTTGGTAGAGACGGGGTTTCTCCATGTTGGCCAGGCTGGTCTCAAACTTCTGA T A SCNN1A Ensembl:ENSG00000111319 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs779140150 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_698,RMVar_hsa_circ_91849,RMVar_hsa_circ_154488,RMVar_hsa_circ_119541,RMVar_hsa_circ_100555,RMVar_hsa_circ_154493,RMVar_hsa_circ_154494 34514 RMVar_ID_34514 Human_SNP_ID_489439494 A-to-I Human chr12 - 6357833 6357833 6357833 CCGCCGTGCCCGGCTAATTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGG CCGCCGTGCCCGGCTAATTTTGTATTTTTAGTTGAGATGGGGTTTCACCATGTTGGCCAGGCTGG T A SCNN1A Ensembl:ENSG00000111319 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1456860141 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_698,RMVar_hsa_circ_91849,RMVar_hsa_circ_154488,RMVar_hsa_circ_119541,RMVar_hsa_circ_100555,RMVar_hsa_circ_154493,RMVar_hsa_circ_154494 34515 RMVar_ID_34515 Human_SNP_ID_489439495 A-to-I Human chr12 - 6357833 6357833 6357833 CCGCCGTGCCCGGCTAATTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGG CCGCCGTGCCCGGCTAATTTTGTATTTTTAGTGGAGATGGGGTTTCACCATGTTGGCCAGGCTGG T C SCNN1A Ensembl:ENSG00000111319 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1456860141 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_698,RMVar_hsa_circ_91849,RMVar_hsa_circ_154488,RMVar_hsa_circ_119541,RMVar_hsa_circ_100555,RMVar_hsa_circ_154493,RMVar_hsa_circ_154494 34516 RMVar_ID_34516 Human_SNP_ID_489439523 A-to-I Human chr12 - 6357946 6357946 6357946 CTGGCCAGGCTGGAGTGCAATGGCGCAATCTCAGCTCATGACAACCTCCACCTCCCAGGTTCAAG CTGGCCAGGCTGGAGTGCAATGGCGCAATCTCGGCTCATGACAACCTCCACCTCCCAGGTTCAAG T C SCNN1A Ensembl:ENSG00000111319 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1380227965 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_698,RMVar_hsa_circ_91849,RMVar_hsa_circ_154488,RMVar_hsa_circ_119541,RMVar_hsa_circ_100555,RMVar_hsa_circ_154493,RMVar_hsa_circ_154494 34517 RMVar_ID_34517 Human_SNP_ID_489439690 A-to-I Human chr12 - 6358776 6358776 6358776 ACCTCACTGTAGCTTTGATTTCCTGGGCTGAAACGATCCTCCTGATTCAGCCTCCCAAGTAGCTG ACCTCACTGTAGCTTTGATTTCCTGGGCTGAAGCGATCCTCCTGATTCAGCCTCCCAAGTAGCTG T C SCNN1A Ensembl:ENSG00000111319 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1468403028 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_698,RMVar_hsa_circ_91849,RMVar_hsa_circ_154488,RMVar_hsa_circ_119541,RMVar_hsa_circ_100555,RMVar_hsa_circ_154493,RMVar_hsa_circ_154494 34518 RMVar_ID_34518 Human_SNP_ID_489439984 A-to-I Human chr12 - 6359862 6359862 6359862 GGAGGCTGAGGCAGGAGGATTGCTTGAACCCAAGAGGTGGAGGTTGCAGTGAGCCGAGATCGCAC GGAGGCTGAGGCAGGAGGATTGCTTGAACCCAGGAGGTGGAGGTTGCAGTGAGCCGAGATCGCAC T C SCNN1A Ensembl:ENSG00000111319 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs941045850 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_698,RMVar_hsa_circ_91849,RMVar_hsa_circ_154488,RMVar_hsa_circ_119541,RMVar_hsa_circ_100555,RMVar_hsa_circ_154493,RMVar_hsa_circ_154494 34519 RMVar_ID_34519 Human_SNP_ID_489463734 A-to-I Human chr12 + 6448657 6448657 6448657 TGTGGTGGCACACACCTGTAATCCCAGCTACTAGGGAGGCTGAGGCAGGAGAATCACTTGAACTC TGTGGTGGCACACACCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACTC A C CD27 Ensembl:ENSG00000139193 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs933080094 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_116205 34520 RMVar_ID_34520 Human_SNP_ID_489463735 A-to-I Human chr12 + 6448657 6448657 6448657 TGTGGTGGCACACACCTGTAATCCCAGCTACTAGGGAGGCTGAGGCAGGAGAATCACTTGAACTC TGTGGTGGCACACACCTGTAATCCCAGCTACTGGGGAGGCTGAGGCAGGAGAATCACTTGAACTC A G CD27 Ensembl:ENSG00000139193 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs933080094 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_116205 34521 RMVar_ID_34521 Human_SNP_ID_489463736 A-to-I Human chr12 + 6448657 6448657 6448657 TGTGGTGGCACACACCTGTAATCCCAGCTACTAGGGAGGCTGAGGCAGGAGAATCACTTGAACTC TGTGGTGGCACACACCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCACTTGAACTC A T CD27 Ensembl:ENSG00000139193 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs933080094 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_116205 34522 RMVar_ID_34522 Human_SNP_ID_489463757 A-to-I Human chr12 + 6448730 6448730 6448730 GAGGTTGCACTGAGCCGAGATCGTGCCACTGCACTCCAACCTGGGCGACAAAGCAAGACTCTGTC GAGGTTGCACTGAGCCGAGATCGTGCCACTGCTCTCCAACCTGGGCGACAAAGCAAGACTCTGTC A T CD27 Ensembl:ENSG00000139193 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1403199119 Functional Loss SNV dbSNP153 33..33 33 - - - 34523 RMVar_ID_34523 Human_SNP_ID_489463884 A-to-I Human chr12 + 6449197 6449197 6449197 TTTTGTATTTTTTGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTCCTGAGCT TTTTGTATTTTTTGTAGAGACGGGGTTTCACCGTGTTGGCCAGGCTGGTCTCAAACTCCTGAGCT A G CD27 Ensembl:ENSG00000139193 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs190599386 Functional Loss SNV dbSNP153 33..33 33 - - - 34524 RMVar_ID_34524 Human_SNP_ID_489463885 A-to-I Human chr12 + 6449197 6449197 6449197 TTTTGTATTTTTTGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTCCTGAGCT TTTTGTATTTTTTGTAGAGACGGGGTTTCACCTTGTTGGCCAGGCTGGTCTCAAACTCCTGAGCT A T CD27 Ensembl:ENSG00000139193 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs190599386 Functional Loss SNV dbSNP153 33..33 33 - - - 34525 RMVar_ID_34525 Human_SNP_ID_489479792 A-to-I Human chr12 + 6505096 6505096 6505096 CATATGCAATTTTTGTTTTGAGACAGAGTTTCACTCTTGTTGCCCAGGCTGGAGTGCAGTGGCAT CATATGCAATTTTTGTTTTGAGACAGAGTTTCCCTCTTGTTGCCCAGGCTGGAGTGCAGTGGCAT A C NCAPD2 Ensembl:ENSG00000010292 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202162612 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90162,RMVar_hsa_circ_154502 34526 RMVar_ID_34526 Human_SNP_ID_489481640 A-to-I Human chr12 + 6511724 6511724 6511724 CTACTCTAGGCCCGGTGCGGTGGCTCACGCCTATAATCCCAGCACTCTGGGAGGCCGAGGCGAGT CTACTCTAGGCCCGGTGCGGTGGCTCACGCCTGTAATCCCAGCACTCTGGGAGGCCGAGGCGAGT A G NCAPD2 Ensembl:ENSG00000010292 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1192515770 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36131,RMVar_hsa_circ_356034,RMVar_hsa_circ_102280,RMVar_hsa_circ_154504,RMVar_hsa_circ_32617,RMVar_hsa_circ_32841,RMVar_hsa_circ_55271,RMVar_hsa_circ_117656,RMVar_hsa_circ_54934,RMVar_hsa_circ_154511,RMVar_hsa_circ_14581 34527 RMVar_ID_34527 Human_SNP_ID_489481657 A-to-I Human chr12 + 6511780 6511780 6511780 GAGGCGAGTGGATCACCTGAGGTCAGGAGTTCAAGACCGGCCTGGCCAACATGGTGAAACCTTGT GAGGCGAGTGGATCACCTGAGGTCAGGAGTTCGAGACCGGCCTGGCCAACATGGTGAAACCTTGT A G NCAPD2 Ensembl:ENSG00000010292 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1324007687 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36131,RMVar_hsa_circ_356034,RMVar_hsa_circ_102280,RMVar_hsa_circ_154504,RMVar_hsa_circ_32617,RMVar_hsa_circ_32841,RMVar_hsa_circ_55271,RMVar_hsa_circ_117656,RMVar_hsa_circ_54934,RMVar_hsa_circ_154511,RMVar_hsa_circ_14581 34528 RMVar_ID_34528 Human_SNP_ID_489482610 A-to-I Human chr12 + 6515330 6515330 6515330 CCTCAGCCTCCCAAGTAGCTGGGACTTCAGGCACATACTACCATGCCTGGCTAATTTTTTTAGTT CCTCAGCCTCCCAAGTAGCTGGGACTTCAGGCGCATACTACCATGCCTGGCTAATTTTTTTAGTT A G NCAPD2 Ensembl:ENSG00000010292 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1314896284 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36131,RMVar_hsa_circ_356034,RMVar_hsa_circ_102280,RMVar_hsa_circ_154504,RMVar_hsa_circ_55271,RMVar_hsa_circ_117656,RMVar_hsa_circ_31767,RMVar_hsa_circ_54934,RMVar_hsa_circ_154511,RMVar_hsa_circ_154517,RMVar_hsa_circ_371401,RMVar_hsa_circ_372707,RMVar_hsa_circ_154516 34529 RMVar_ID_34529 Human_SNP_ID_489482798 A-to-I Human chr12 + 6516069 6516069 6516069 CAAAAAAAAATTAGCTGGGTGTGGTGGCGCGCACCTGTAATCCTAGCTACTCGGGAGGCTGAAGT CAAAAAAAAATTAGCTGGGTGTGGTGGCGCGCGCCTGTAATCCTAGCTACTCGGGAGGCTGAAGT A G NCAPD2 Ensembl:ENSG00000010292 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1328452151 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36131,RMVar_hsa_circ_356034,RMVar_hsa_circ_102280,RMVar_hsa_circ_154504,RMVar_hsa_circ_55271,RMVar_hsa_circ_117656,RMVar_hsa_circ_31767,RMVar_hsa_circ_54934,RMVar_hsa_circ_154511,RMVar_hsa_circ_154517,RMVar_hsa_circ_371401,RMVar_hsa_circ_372707,RMVar_hsa_circ_154516 34530 RMVar_ID_34530 Human_SNP_ID_489484176 A-to-I Human chr12 + 6520359 6520359 6520359 GATCTCCCAGGCTCAAGTGATCCTCCCACCTCAGCTCCCTCGAGTAGCTGAGACCACAGGCACAC GATCTCCCAGGCTCAAGTGATCCTCCCACCTCCGCTCCCTCGAGTAGCTGAGACCACAGGCACAC A C NCAPD2 Ensembl:ENSG00000010292 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1289534728 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36131,RMVar_hsa_circ_102280,RMVar_hsa_circ_154504,RMVar_hsa_circ_117656,RMVar_hsa_circ_13094,RMVar_hsa_circ_154511,RMVar_hsa_circ_154517,RMVar_hsa_circ_371401,RMVar_hsa_circ_372707,RMVar_hsa_circ_154516,RMVar_hsa_circ_332251,RMVar_hsa_circ_43599,RMVar_hsa_circ_30144,RMVar_hsa_circ_123765,RMVar_hsa_circ_154519,RMVar_hsa_circ_154520,RMVar_hsa_circ_112971 34531 RMVar_ID_34531 Human_SNP_ID_489485428 A-to-I Human chr12 + 6524528 6524528 6524528 AAAATTAGCCAGGTGTGGTGGTGGGCACCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGACA AAAATTAGCCAGGTGTGGTGGTGGGCACCTGTGGTCCCAGCTACTTGGGAGGCTGAGGCAGGACA A G NCAPD2 Ensembl:ENSG00000010292 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs754723801 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76078,RMVar_hsa_circ_103761,RMVar_hsa_circ_154521,RMVar_hsa_circ_123089,RMVar_hsa_circ_112593,RMVar_hsa_circ_154526,RMVar_hsa_circ_154527,RMVar_hsa_circ_154528,RMVar_hsa_circ_95313,RMVar_hsa_circ_154529 34532 RMVar_ID_34532 Human_SNP_ID_489487677 A-to-I Human chr12 + 6531694 6531694 6531694 GGGCGTATTGGCGTGCGCCTGTAATCCCAGCTACTCAAGAGGCTGAGGCAGGAGAATCGCCTGAA GGGCGTATTGGCGTGCGCCTGTAATCCCAGCTGCTCAAGAGGCTGAGGCAGGAGAATCGCCTGAA A G NCAPD2 Ensembl:ENSG00000010292 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1224654653 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2865663 RMVar_hsa_circ_103761,RMVar_hsa_circ_154521,RMVar_hsa_circ_80445,RMVar_hsa_circ_154535 34533 RMVar_ID_34533 Human_SNP_ID_489487694 A-to-I Human chr12 + 6531759 6531757 6531759 CCCAGAGGCGGAGGTTGTAGTGAGCCGAAATCACACCATTGCACTCCAGCTTGGGCAACAATAGC CCCAGAGGCGGAGGTTGTAGTGAGCCGAAAT__CACCATTGCACTCCAGCTTGGGCAACAATAGC TCA T NCAPD2 Ensembl:ENSG00000010292 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs777501675 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_18631554,Human_RBP_ID_23158957,Human_RBP_ID_23570488,Human_RBP_ID_24993297,Human_RBP_ID_26805363 Human_miRNA_ID_211432,Human_miRNA_ID_220951,Human_miRNA_ID_759484,Human_miRNA_ID_764424,Human_miRNA_ID_1072091,Human_miRNA_ID_1323984,Human_miRNA_ID_2019590,Human_miRNA_ID_2024685,Human_miRNA_ID_2311305,Human_miRNA_ID_2313322,Human_miRNA_ID_2499416,Human_miRNA_ID_2607200,Human_miRNA_ID_2655107 RMVar_hsa_circ_103761,RMVar_hsa_circ_154521,RMVar_hsa_circ_80445,RMVar_hsa_circ_154535 34534 RMVar_ID_34534 Human_SNP_ID_489496254 A-to-I Human chr12 - 6558025 6558025 6558025 GCGATTCTTGTGCCTCAGACTCCCAAGTAGCTAGGATTACAGGTGTGTACCACCATCCCTGGCTA GCGATTCTTGTGCCTCAGACTCCCAAGTAGCTGGGATTACAGGTGTGTACCACCATCCCTGGCTA T C NOP2,AC006064.6 Ensembl:ENSG00000111641,Ensembl:ENSG00000285238 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1401751681 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1329043 RMVar_hsa_circ_154572,RMVar_hsa_circ_97889,RMVar_hsa_circ_127483,RMVar_hsa_circ_114513,RMVar_hsa_circ_154573,RMVar_hsa_circ_154574 34535 RMVar_ID_34535 Human_SNP_ID_489496287 A-to-I Human chr12 - 6558094 6558094 6558094 CTTTGTCGCTCAGGCTGGACTGCAGTGGTGCAATCTCAGCTCATTGCAACCTCCACCTTCCAGGT CTTTGTCGCTCAGGCTGGACTGCAGTGGTGCAGTCTCAGCTCATTGCAACCTCCACCTTCCAGGT T C NOP2,AC006064.6 Ensembl:ENSG00000111641,Ensembl:ENSG00000285238 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1283126632 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1329042,Human_Splice_Rec_1329043,Human_Splice_Rec_1329170 RMVar_hsa_circ_154572,RMVar_hsa_circ_97889,RMVar_hsa_circ_127483,RMVar_hsa_circ_114513,RMVar_hsa_circ_154573,RMVar_hsa_circ_154574 34536 RMVar_ID_34536 Human_SNP_ID_489496288 A-to-I Human chr12 - 6558095 6558095 6558095 GCTTTGTCGCTCAGGCTGGACTGCAGTGGTGCAATCTCAGCTCATTGCAACCTCCACCTTCCAGG GCTTTGTCGCTCAGGCTGGACTGCAGTGGTGCGATCTCAGCTCATTGCAACCTCCACCTTCCAGG T C NOP2,AC006064.6 Ensembl:ENSG00000111641,Ensembl:ENSG00000285238 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1313660890 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1329042,Human_Splice_Rec_1329043,Human_Splice_Rec_1329170 RMVar_hsa_circ_154572,RMVar_hsa_circ_97889,RMVar_hsa_circ_127483,RMVar_hsa_circ_114513,RMVar_hsa_circ_154573,RMVar_hsa_circ_154574 34537 RMVar_ID_34537 Human_SNP_ID_489496426 A-to-I Human chr12 - 6558365 6558365 6558365 CGGAGGCTGAGGCAGGAGAATTGCTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCCGAGATCACA CGGAGGCTGAGGCAGGAGAATTGCTTGAACCCTGGAGGCAGAGGTTGCAGTGAGCCGAGATCACA T A NOP2,AC006064.6 Ensembl:ENSG00000111641,Ensembl:ENSG00000285238 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1481078850 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_154572,RMVar_hsa_circ_97889,RMVar_hsa_circ_127483,RMVar_hsa_circ_114513,RMVar_hsa_circ_154573,RMVar_hsa_circ_154574 34538 RMVar_ID_34538 Human_SNP_ID_489501824 A-to-I Human chr12 - 6576165 6576165 6576165 TTTAGTAGAGACAGGGTTTCAGCATGTTGGCCAGGATGGTCTCGATCTCTTGACCTCATGTTCTG TTTAGTAGAGACAGGGTTTCAGCATGTTGGCCGGGATGGTCTCGATCTCTTGACCTCATGTTCTG T C CHD4,AC006064.6 Ensembl:ENSG00000111642,Ensembl:ENSG00000285238 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1023439591 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100510,RMVar_hsa_circ_102778,RMVar_hsa_circ_154580,RMVar_hsa_circ_154581 34539 RMVar_ID_34539 Human_SNP_ID_489501839 A-to-I Human chr12 - 6576222 6576222 6576222 CTCCCGAGTAGCTGGGACAACAGGCGTGTGCCACCACGCCCAGCTAATTTTTGTATTTTTAGTAG CTCCCGAGTAGCTGGGACAACAGGCGTGTGCCGCCACGCCCAGCTAATTTTTGTATTTTTAGTAG T C CHD4,AC006064.6 Ensembl:ENSG00000111642,Ensembl:ENSG00000285238 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1259447637 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100510,RMVar_hsa_circ_102778,RMVar_hsa_circ_154580,RMVar_hsa_circ_154581 34540 RMVar_ID_34540 Human_SNP_ID_489501886 A-to-I Human chr12 - 6576428 6576428 6576428 CACCTGTAGTTCCAGCTACTTAGGAGGCTGCAATGAGCCTAGATTGTGCCATTGCACTCCAGCCT CACCTGTAGTTCCAGCTACTTAGGAGGCTGCAGTGAGCCTAGATTGTGCCATTGCACTCCAGCCT T C CHD4,AC006064.6 Ensembl:ENSG00000111642,Ensembl:ENSG00000285238 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs867438885 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8382008,Human_RBP_ID_12010440 RMVar_hsa_circ_100510,RMVar_hsa_circ_102778,RMVar_hsa_circ_154580,RMVar_hsa_circ_154581 34541 RMVar_ID_34541 Human_SNP_ID_489504881 A-to-I Human chr12 - 6585703 6585703 6585703 CTCACTGCAACCTCCGCCTCCCGGGTTCAAGCAGTTCTCTTGCCTCAGCCTCCCGAATAGCTGGG CTCACTGCAACCTCCGCCTCCCGGGTTCAAGCGGTTCTCTTGCCTCAGCCTCCCGAATAGCTGGG T C CHD4,AC006064.6 Ensembl:ENSG00000111642,Ensembl:ENSG00000285238 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs554127261 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_154585,RMVar_hsa_circ_93404,RMVar_hsa_circ_267036,RMVar_hsa_circ_77106,RMVar_hsa_circ_154588,RMVar_hsa_circ_267741,RMVar_hsa_circ_92656,RMVar_hsa_circ_51264,RMVar_hsa_circ_154589 34542 RMVar_ID_34542 Human_SNP_ID_489505166 A-to-I Human chr12 - 6586533 6586533 6586533 AATGTTTTTAGAGATGTCTTGCTATGTTGCCCAGGATGGTCTTGAACTCCTGGCCTTAAGCAGTT AATGTTTTTAGAGATGTCTTGCTATGTTGCCCGGGATGGTCTTGAACTCCTGGCCTTAAGCAGTT T C CHD4,AC006064.6 Ensembl:ENSG00000111642,Ensembl:ENSG00000285238 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs767972147 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8382022,Human_RBP_ID_17561358 RMVar_hsa_circ_154585,RMVar_hsa_circ_93404,RMVar_hsa_circ_267036,RMVar_hsa_circ_77106,RMVar_hsa_circ_154588,RMVar_hsa_circ_267741,RMVar_hsa_circ_92656,RMVar_hsa_circ_51264,RMVar_hsa_circ_154589 34543 RMVar_ID_34543 Human_SNP_ID_489505235 A-to-I Human chr12 - 6586773 6586773 6586773 GAATTGCTTGAACCCAGGAGGCGGAGGTTGCAATGAGCTGAGATTGCGCCACTGCATTCCAGCCT GAATTGCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCTGAGATTGCGCCACTGCATTCCAGCCT T C CHD4,AC006064.6 Ensembl:ENSG00000111642,Ensembl:ENSG00000285238 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1330743607 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_154585,RMVar_hsa_circ_93404,RMVar_hsa_circ_267036,RMVar_hsa_circ_77106,RMVar_hsa_circ_154588,RMVar_hsa_circ_267741,RMVar_hsa_circ_92656,RMVar_hsa_circ_51264,RMVar_hsa_circ_154589 34544 RMVar_ID_34544 Human_SNP_ID_489505243 A-to-I Human chr12 - 6586803 6586803 6586803 GTCCCAGGTGTTCGGGAGGCTGAGGCAGGAGAATTGCTTGAACCCAGGAGGCGGAGGTTGCAATG GTCCCAGGTGTTCGGGAGGCTGAGGCAGGAGAGTTGCTTGAACCCAGGAGGCGGAGGTTGCAATG T C CHD4,AC006064.6 Ensembl:ENSG00000111642,Ensembl:ENSG00000285238 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs987956234 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_154585,RMVar_hsa_circ_93404,RMVar_hsa_circ_267036,RMVar_hsa_circ_77106,RMVar_hsa_circ_154588,RMVar_hsa_circ_267741,RMVar_hsa_circ_92656,RMVar_hsa_circ_51264,RMVar_hsa_circ_154589 34545 RMVar_ID_34545 Human_SNP_ID_489524007 A-to-I Human chr12 - 6647639 6647639 6647639 GAGGTTGTAGTGAGCCGAGATCGCACCACTGCACTCCAGCCTGGGCGACAGAGTAGGACTCCGTC GAGGTTGTAGTGAGCCGAGATCGCACCACTGCGCTCCAGCCTGGGCGACAGAGTAGGACTCCGTC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1328507174 Functional Loss SNV dbSNP153 33..33 33 - - - 34546 RMVar_ID_34546 Human_SNP_ID_489532784 A-to-I Human chr12 - 6680184 6680184 6680184 AAGGTGGGCTGATCCCTTGAGCCTAGGAGTTCAAGACCAGCCTGGGCAACATGGAAAAACCGTGT AAGGTGGGCTGATCCCTTGAGCCTAGGAGTTCCAGACCAGCCTGGGCAACATGGAAAAACCGTGT T G ZNF384 Ensembl:ENSG00000126746 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs993632482 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17560992 RMVar_hsa_circ_331498,RMVar_hsa_circ_154606,RMVar_hsa_circ_295570,RMVar_hsa_circ_154611,RMVar_hsa_circ_315312 34547 RMVar_ID_34547 Human_SNP_ID_489547038 A-to-I Human chr12 + 6725935 6725935 6725935 GCACTTGGCTGGGTGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGAAGGCCAAGGCAGGTGG GCACTTGGCTGGGTGCGGTGGCTCATGCCTGTGATCCCAGCACTTTGGAAGGCCAAGGCAGGTGG A G COPS7A Ensembl:ENSG00000111652 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1161271211 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1331840,Human_Splice_Rec_1331948 RMVar_hsa_circ_12814,RMVar_hsa_circ_36664,RMVar_hsa_circ_289996 34548 RMVar_ID_34548 Human_SNP_ID_489547562 A-to-I Human chr12 + 6727686 6727686 6727686 TTCAACTCTGAATTTAGGGTAGGAATTGGATGACGTATGGAGCAAGAGGGCATTGTGGTTTGGGA TTCAACTCTGAATTTAGGGTAGGAATTGGATGGCGTATGGAGCAAGAGGGCATTGTGGTTTGGGA A G COPS7A Ensembl:ENSG00000111652 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7138427 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1331896 GWAS_ID_3862 RMVar_hsa_circ_12814,RMVar_hsa_circ_36664,RMVar_hsa_circ_289996 34549 RMVar_ID_34549 Human_SNP_ID_489551046 A-to-I Human chr12 + 6739560 6739560 6739560 TCAGGAGGCGAAGCTTCCAGAGAGCCGAGATCACACCACTGCACTCCAGCCTGGGCGACAGAGCG TCAGGAGGCGAAGCTTCCAGAGAGCCGAGATCCCACCACTGCACTCCAGCCTGGGCGACAGAGCG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017956817 Functional Loss SNV dbSNP153 33..33 33 - - - 34550 RMVar_ID_34550 Human_SNP_ID_489551047 A-to-I Human chr12 + 6739560 6739560 6739560 TCAGGAGGCGAAGCTTCCAGAGAGCCGAGATCACACCACTGCACTCCAGCCTGGGCGACAGAGCG TCAGGAGGCGAAGCTTCCAGAGAGCCGAGATCGCACCACTGCACTCCAGCCTGGGCGACAGAGCG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017956817 Functional Loss SNV dbSNP153 33..33 33 - - - 34551 RMVar_ID_34551 Human_SNP_ID_489583541 A-to-I Human chr12 - 6849112 6849112 6849112 ATTCTTGGAACTGGACGACTTCTGAAAACTGGAGGACGAGCATGGGAGCAAGGCCAGGACCATGA ATTCTTGGAACTGGACGACTTCTGAAAACTGGGGGACGAGCATGGGAGCAAGGCCAGGACCATGA T C CDCA3 Ensembl:ENSG00000111665 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs372805520 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_426812,Human_RBP_ID_1476603,Human_RBP_ID_1800270,Human_RBP_ID_3412747,Human_RBP_ID_4259346,Human_RBP_ID_6214480,Human_RBP_ID_8247821,Human_RBP_ID_9364621,Human_RBP_ID_12019268,Human_RBP_ID_18526756,Human_RBP_ID_18632519,Human_RBP_ID_22039816,Human_RBP_ID_22910957 Human_Splice_Rec_1332562,Human_Splice_Rec_1332572,Human_Splice_Rec_1332580,Human_Splice_Rec_1332586,Human_Splice_Rec_1332594,Human_Splice_Rec_1332600,Human_Splice_Rec_1332606 34552 RMVar_ID_34552 Human_SNP_ID_489594377 A-to-I Human chr12 + 6885241 6885241 6885241 AACTAGCACCTTTGAAAAGTAAAATGATCTATACAAGCTCCAAGGATGCAATCAAAAAGAAATTT AACTAGCACCTTTGAAAAGTAAAATGATCTATGCAAGCTCCAAGGATGCAATCAAAAAGAAATTT A G DSTNP2,LRRC23 Ensembl:ENSG00000248593,Ensembl:ENSG00000010626 Pseudogene,Protein coding exon,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs879957731 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1863471,Human_miRNA_ID_1873499,Human_miRNA_ID_1884180 34553 RMVar_ID_34553 Human_SNP_ID_489594430 A-to-I Human chr12 + 6885426 6885417 6885426 CAGGCTGGAGTGCAGTGACAGGATCTCGGCTCACTGCAACCTCTGCCTCCCGGGTTCAAGTGATT CAGGCTGGAGTGCAGTGACAGGAT_________CTGCAACCTCTGCCTCCCGGGTTCAAGTGATT TCTCGGCTCA T DSTNP2,LRRC23 Ensembl:ENSG00000248593,Ensembl:ENSG00000010626 Pseudogene,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334985692 Functional Loss DEL dbSNP153 25..33 33 - - - Human_RBP_ID_17358165 34554 RMVar_ID_34554 Human_SNP_ID_489594459 A-to-I Human chr12 + 6885547 6885547 6885547 AATTTTTGTATTCTTAGTAGAGTCAGGGTTTCACCATATTGGTCAGGCTGGTCTCGAACTCCTGA AATTTTTGTATTCTTAGTAGAGTCAGGGTTTCGCCATATTGGTCAGGCTGGTCTCGAACTCCTGA A G DSTNP2,LRRC23 Ensembl:ENSG00000248593,Ensembl:ENSG00000010626 Pseudogene,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1458158474 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9710416 34555 RMVar_ID_34555 Human_SNP_ID_489594461 A-to-I Human chr12 + 6885552 6885552 6885552 TTGTATTCTTAGTAGAGTCAGGGTTTCACCATATTGGTCAGGCTGGTCTCGAACTCCTGACCTCG TTGTATTCTTAGTAGAGTCAGGGTTTCACCATGTTGGTCAGGCTGGTCTCGAACTCCTGACCTCG A G DSTNP2,LRRC23 Ensembl:ENSG00000248593,Ensembl:ENSG00000010626 Pseudogene,Protein coding exon,intron GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490829,GSM3490830,GSM3490831 Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,EC109 cell line - 31158229,32596459 RNA-Seq:(High) rs1161227045 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9710416 34556 RMVar_ID_34556 Human_SNP_ID_489594477 A-to-I Human chr12 + 6885609 6885609 6885609 TGACCTCGTGATTTGCCCTCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCAGCATGC TGACCTCGTGATTTGCCCTCCTTGGCCTCCCACAGTGCTGGGATTACAGGCGTGAGCCAGCATGC A C DSTNP2,LRRC23 Ensembl:ENSG00000248593,Ensembl:ENSG00000010626 Pseudogene,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1325393978 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3422013,Human_RBP_ID_9710416 34557 RMVar_ID_34557 Human_SNP_ID_489595349 A-to-I Human chr12 + 6888861 6888861 6888861 GCGGCTGGAGTAAAGTGGCTCAATCTCTGCTCACTGCAAACTCTCCCTCCCAGGTTCAAGCAATT GCGGCTGGAGTAAAGTGGCTCAATCTCTGCTCGCTGCAAACTCTCCCTCCCAGGTTCAAGCAATT A G LRRC23 Ensembl:ENSG00000010626 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1189756237 Functional Loss SNV dbSNP153 33..33 33 - - - 34558 RMVar_ID_34558 Human_SNP_ID_489596265 A-to-I Human chr12 + 6892191 6892191 6892191 TCAAGCGATTCTGTTGCCTCAGCCTCCCGAGTAGCTGGGCTTACAGGCATGCGCCACCACGCCCA TCAAGCGATTCTGTTGCCTCAGCCTCCCGAGTCGCTGGGCTTACAGGCATGCGCCACCACGCCCA A C LRRC23 Ensembl:ENSG00000010626 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934473038 Functional Loss SNV dbSNP153 33..33 33 - - - 34559 RMVar_ID_34559 Human_SNP_ID_489596266 A-to-I Human chr12 + 6892191 6892191 6892191 TCAAGCGATTCTGTTGCCTCAGCCTCCCGAGTAGCTGGGCTTACAGGCATGCGCCACCACGCCCA TCAAGCGATTCTGTTGCCTCAGCCTCCCGAGTGGCTGGGCTTACAGGCATGCGCCACCACGCCCA A G LRRC23 Ensembl:ENSG00000010626 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934473038 Functional Loss SNV dbSNP153 33..33 33 - - - 34560 RMVar_ID_34560 Human_SNP_ID_489596419 A-to-I Human chr12 + 6892809 6892809 6892809 GAAACTGAAGAACTCAAGATCTATTGGAGGCCAAGTGCAAGTTGCTCATGCCTGTAATCCTAGCA GAAACTGAAGAACTCAAGATCTATTGGAGGCCCAGTGCAAGTTGCTCATGCCTGTAATCCTAGCA A C LRRC23 Ensembl:ENSG00000010626 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1267637551 Functional Loss SNV dbSNP153 33..33 33 - - - 34561 RMVar_ID_34561 Human_SNP_ID_489601844 A-to-I Human chr12 + 6910435 6910435 6910435 TGTTTCTACAGAAGTGAAAATAATGGCCCGGCATGGTGGCTCACACCTGTAGTTCTAGCACTTTG TGTTTCTACAGAAGTGAAAATAATGGCCCGGCGTGGTGGCTCACACCTGTAGTTCTAGCACTTTG A G LRRC23 Ensembl:ENSG00000010626 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1301168244 Functional Loss SNV dbSNP153 33..33 33 - - - 34562 RMVar_ID_34562 Human_SNP_ID_489602270 A-to-I Human chr12 + 6912285 6912285 6912285 AATCCCTCCTCCTCAGCTAAGTAGCAAGGACTACAGGTGTATGCCATCACGCCCAGCTAATTTTT AATCCCTCCTCCTCAGCTAAGTAGCAAGGACTGCAGGTGTATGCCATCACGCCCAGCTAATTTTT A G LRRC23 Ensembl:ENSG00000010626 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1160316988 Functional Loss SNV dbSNP153 33..33 33 - - - 34563 RMVar_ID_34563 Human_SNP_ID_489604762 A-to-I Human chr12 + 6920529 6920529 6920529 TCAAGCGATTCTTCTGCCTCAGCCTCCCGAATAGCTGGGATTACAGGCATGTGCCACCATGCCTG TCAAGCGATTCTTCTGCCTCAGCCTCCCGAATTGCTGGGATTACAGGCATGTGCCACCATGCCTG A T ENO2 Ensembl:ENSG00000111674 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs782248206 Functional Loss SNV dbSNP153 33..33 33 - - - 34564 RMVar_ID_34564 Human_SNP_ID_489604903 A-to-I Human chr12 + 6920987 6920987 6920987 TTTTGTATTTTTAGTAGAGATGGGGTTTTACTATGTTAGCCAGGGAACTCCTATCCTCAAGTGAT TTTTGTATTTTTAGTAGAGATGGGGTTTTACTCTGTTAGCCAGGGAACTCCTATCCTCAAGTGAT A C ENO2 Ensembl:ENSG00000111674 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1007183735 Functional Loss SNV dbSNP153 33..33 33 - - - 34565 RMVar_ID_34565 Human_SNP_ID_489604904 A-to-I Human chr12 + 6920987 6920987 6920987 TTTTGTATTTTTAGTAGAGATGGGGTTTTACTATGTTAGCCAGGGAACTCCTATCCTCAAGTGAT TTTTGTATTTTTAGTAGAGATGGGGTTTTACTGTGTTAGCCAGGGAACTCCTATCCTCAAGTGAT A G ENO2 Ensembl:ENSG00000111674 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1007183735 Functional Loss SNV dbSNP153 33..33 33 - - - 34566 RMVar_ID_34566 Human_SNP_ID_489604972 A-to-I Human chr12 + 6921345 6921329 6921345 GATTGGGGAGGTGGAGGTTGCAGTGAGCTGAGATTGTGCCACTGCACTCCAGCCTGGATGACAGA GATTGGGGAGGTGGAGG________________TTGTGCCACTGCACTCCAGCCTGGATGACAGA GTTGCAGTGAGCTGAGA G ENO2 Ensembl:ENSG00000111674 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1374305981 Functional Loss DEL dbSNP153 18..33 33 - - - 34567 RMVar_ID_34567 Human_SNP_ID_489614781 A-to-I Human chr12 + 6949875 6949875 6949875 TCACTCTGTTGCCCAGGCTGGAGTGCGGTGGCATGATCTCGGCTCACTGCAACCTCCACCTCCTG TCACTCTGTTGCCCAGGCTGGAGTGCGGTGGCGTGATCTCGGCTCACTGCAACCTCCACCTCCTG A G PTPN6 Ensembl:ENSG00000111679 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1456986559 Functional Loss SNV dbSNP153 33..33 33 - - - 34568 RMVar_ID_34568 Human_SNP_ID_489620249 A-to-I Human chr12 - 6967675 6967675 6967675 AGGCCGAGGGTGAGGCCGAGGCTGCCAAGATGATATCCTTCTGCTGGAGAGATCTCAGCCCAGCC AGGCCGAGGGTGAGGCCGAGGCTGCCAAGATGCTATCCTTCTGCTGGAGAGATCTCAGCCCAGCC T G PHB2 Ensembl:ENSG00000215021 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs112401532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_427512,Human_RBP_ID_17830213,Human_RBP_ID_18633131,Human_RBP_ID_22574100,Human_RBP_ID_22908969,Human_RBP_ID_27425022 RMVar_hsa_circ_6926,RMVar_hsa_circ_121658,RMVar_hsa_circ_125056,RMVar_hsa_circ_112548,RMVar_hsa_circ_116151,RMVar_hsa_circ_154674,RMVar_hsa_circ_154678,RMVar_hsa_circ_89625,RMVar_hsa_circ_93446,RMVar_hsa_circ_154679,RMVar_hsa_circ_154676,RMVar_hsa_circ_154677,RMVar_hsa_circ_154675,RMVar_hsa_circ_154680,RMVar_hsa_circ_374995,RMVar_hsa_circ_311995,RMVar_hsa_circ_154681 34569 RMVar_ID_34569 Human_SNP_ID_489630444 A-to-I Human chr12 - 7007109 7007109 7007109 AACCCGGGAGGCAGAGGTTGCAGTGAGCCGAGATCGCGCCATTGCACTCCACCTGGGCAACAAGA AACCCGGGAGGCAGAGGTTGCAGTGAGCCGAGGTCGCGCCATTGCACTCCACCTGGGCAACAAGA T C LPCAT3 Ensembl:ENSG00000111684 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1555156898 Functional Loss SNV dbSNP153 33..33 33 - - - 34570 RMVar_ID_34570 Human_SNP_ID_489652546 A-to-I Human chr12 - 7095178 7095178 7095178 CTGGGAGGCGGAGGTTGCAGTGAGCTAAGATCACGCCACTGCACTCCAGCCTGCGGACAGACCAA CTGGGAGGCGGAGGTTGCAGTGAGCTAAGATCGCGCCACTGCACTCCAGCCTGCGGACAGACCAA T C C1RL Ensembl:ENSG00000139178 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1266814578 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1334146 34571 RMVar_ID_34571 Human_SNP_ID_489653236 A-to-I Human chr12 - 7097337 7097337 7097337 CGGAGGTTGCAGTGAGCCGAGATCGCGCAAGTACGCTCCAGTCTGGGCAACAAGAGCGAAACTCG CGGAGGTTGCAGTGAGCCGAGATCGCGCAAGTGCGCTCCAGTCTGGGCAACAAGAGCGAAACTCG T C C1RL Ensembl:ENSG00000139178 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs775407678 Functional Loss SNV dbSNP153 33..33 33 - - - 34572 RMVar_ID_34572 Human_SNP_ID_489653278 A-to-I Human chr12 - 7097486 7097486 7097486 CTGAGGTCAGGAGTTTCAGACCAGCCTGGCCCACATGATGAAACCCCGTCTCTACTAAAAAATAC CTGAGGTCAGGAGTTTCAGACCAGCCTGGCCCGCATGATGAAACCCCGTCTCTACTAAAAAATAC T C C1RL Ensembl:ENSG00000139178 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1413792146 Functional Loss SNV dbSNP153 33..33 33 - - - 34573 RMVar_ID_34573 Human_SNP_ID_489653293 A-to-I Human chr12 - 7097555 7097555 7097555 GATCCCGGCCAGGCGCGGTGCCTCACGCCTGTAATCCCAGCACTTTGGGAGGCAGAGGCGGGTGG GATCCCGGCCAGGCGCGGTGCCTCACGCCTGTTATCCCAGCACTTTGGGAGGCAGAGGCGGGTGG T A C1RL Ensembl:ENSG00000139178 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1013334601 Functional Loss SNV dbSNP153 33..33 33 - - - 34574 RMVar_ID_34574 Human_SNP_ID_489653437 A-to-I Human chr12 - 7098123 7098123 7098123 GGGACTACAGGCGCCCGCCACCACGGCCGGCTAATTTTTTTTTGTATTTTTTAGTAGAGACGGGG GGGACTACAGGCGCCCGCCACCACGGCCGGCTCATTTTTTTTTGTATTTTTTAGTAGAGACGGGG T G C1RL Ensembl:ENSG00000139178 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1416156319 Functional Loss SNV dbSNP153 33..33 33 - - - 34575 RMVar_ID_34575 Human_SNP_ID_489659794 A-to-I Human chr12 + 7125181 7125181 7125181 CGCCCGCCACCGCTTCCTAAAGTGCTGTGACTATAGGCATGAACCATCACACCCAGCTTTCCACT CGCCCGCCACCGCTTCCTAAAGTGCTGTGACTGTAGGCATGAACCATCACACCCAGCTTTCCACT A G C1RL-AS1 RNACentral:URS00008C0582 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1052251284 Functional Loss SNV dbSNP153 33..33 33 - - - 34576 RMVar_ID_34576 Human_SNP_ID_489776891 A-to-I Human chr12 + 7607036 7607036 7607036 GAAAGTATCCGTAAATGGAGAGAAGAGCAAACAGAACGCTTGGAAGCCCTTGATGCCAATTCTCA GAAAGTATCCGTAAATGGAGAGAAGAGCAAACGGAACGCTTGGAAGCCCTTGATGCCAATTCTCA A G AC006927.1 Ensembl:ENSG00000255977 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879063602 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23575580 34577 RMVar_ID_34577 Human_SNP_ID_489776900 A-to-I Human chr12 + 7607068 7607068 7607068 AGAACGCTTGGAAGCCCTTGATGCCAATTCTCAGAAGCAAGAAGCAGAGTGGAAAGAAAAGGCAA AGAACGCTTGGAAGCCCTTGATGCCAATTCTCGGAAGCAAGAAGCAGAGTGGAAAGAAAAGGCAA A G AC006927.1 Ensembl:ENSG00000255977 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879042960 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17358195,Human_RBP_ID_18527209 Human_miRNA_ID_1896592 34578 RMVar_ID_34578 Human_SNP_ID_489867305 A-to-I Human chr12 - 7923426 7923426 7923426 ACTTCTTAGTAGAGACTGTGTTTCACCATGTTAGCCAGGCTGGTCTCCAACTCTTGACCTCAGAT ACTTCTTAGTAGAGACTGTGTTTCACCATGTTGGCCAGGCTGGTCTCCAACTCTTGACCTCAGAT T C SLC2A3 Ensembl:ENSG00000059804 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1296971479 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17561014 RMVar_hsa_circ_101124,RMVar_hsa_circ_103742,RMVar_hsa_circ_124122,RMVar_hsa_circ_95032,RMVar_hsa_circ_154727,RMVar_hsa_circ_154729,RMVar_hsa_circ_154728,RMVar_hsa_circ_154726 34579 RMVar_ID_34579 Human_SNP_ID_489867329 A-to-I Human chr12 - 7923493 7923493 7923493 CTGCTGCCTCAGCCTCCCAGGTAGCTGGGATTATAGGCACGTGCCACCACGCTCAGCTAATTTTT CTGCTGCCTCAGCCTCCCAGGTAGCTGGGATTGTAGGCACGTGCCACCACGCTCAGCTAATTTTT T C SLC2A3 Ensembl:ENSG00000059804 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs899581004 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101124,RMVar_hsa_circ_103742,RMVar_hsa_circ_124122,RMVar_hsa_circ_95032,RMVar_hsa_circ_154727,RMVar_hsa_circ_154729,RMVar_hsa_circ_154728,RMVar_hsa_circ_154726 34580 RMVar_ID_34580 Human_SNP_ID_489867344 A-to-I Human chr12 - 7923563 7923563 7923563 GTCACCAGGCTGGAGAGCAGTGGCAGGATCTCAGCTCACTGCAACCTCTGCCTCCTGGGCTTAAG GTCACCAGGCTGGAGAGCAGTGGCAGGATCTCGGCTCACTGCAACCTCTGCCTCCTGGGCTTAAG T C SLC2A3 Ensembl:ENSG00000059804 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1475440642 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101124,RMVar_hsa_circ_103742,RMVar_hsa_circ_124122,RMVar_hsa_circ_95032,RMVar_hsa_circ_154727,RMVar_hsa_circ_154729,RMVar_hsa_circ_154728,RMVar_hsa_circ_154726 34581 RMVar_ID_34581 Human_SNP_ID_489867348 A-to-I Human chr12 - 7923592 7923592 7923592 ATTTTTTTTTTGAGACAGGGTTTCACTCTGTCACCAGGCTGGAGAGCAGTGGCAGGATCTCAGCT ATTTTTTTTTTGAGACAGGGTTTCACTCTGTCTCCAGGCTGGAGAGCAGTGGCAGGATCTCAGCT T A SLC2A3 Ensembl:ENSG00000059804 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928061519 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101124,RMVar_hsa_circ_103742,RMVar_hsa_circ_124122,RMVar_hsa_circ_95032,RMVar_hsa_circ_154727,RMVar_hsa_circ_154729,RMVar_hsa_circ_154728,RMVar_hsa_circ_154726 34582 RMVar_ID_34582 Human_SNP_ID_489867456 A-to-I Human chr12 - 7923842 7923842 7923842 ATTGCTTGAACCCAGGAGGCAGAGGTTGTGGTAAGTTGAGATGGTGCCATTGCACTCCAGCCTGA ATTGCTTGAACCCAGGAGGCAGAGGTTGTGGTGAGTTGAGATGGTGCCATTGCACTCCAGCCTGA T C SLC2A3 Ensembl:ENSG00000059804 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1442368080 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101124,RMVar_hsa_circ_103742,RMVar_hsa_circ_124122,RMVar_hsa_circ_95032,RMVar_hsa_circ_154727,RMVar_hsa_circ_154729,RMVar_hsa_circ_154728,RMVar_hsa_circ_154726 34583 RMVar_ID_34583 Human_SNP_ID_489868985 A-to-I Human chr12 - 7929557 7929557 7929557 AGGAGGCTGAGGTAAGAGGATCACTTGAGCTCAGGAGTTTCAGGTTGCAGTGAGCTATAATTATG AGGAGGCTGAGGTAAGAGGATCACTTGAGCTCGGGAGTTTCAGGTTGCAGTGAGCTATAATTATG T C SLC2A3 Ensembl:ENSG00000059804 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1266877006 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124122,RMVar_hsa_circ_95032,RMVar_hsa_circ_154727,RMVar_hsa_circ_154726,RMVar_hsa_circ_68152 34584 RMVar_ID_34584 Human_SNP_ID_489868987 A-to-I Human chr12 - 7929562 7929562 7929562 TACTCAGGAGGCTGAGGTAAGAGGATCACTTGAGCTCAGGAGTTTCAGGTTGCAGTGAGCTATAA TACTCAGGAGGCTGAGGTAAGAGGATCACTTGTGCTCAGGAGTTTCAGGTTGCAGTGAGCTATAA T A SLC2A3 Ensembl:ENSG00000059804 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs112237103 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124122,RMVar_hsa_circ_95032,RMVar_hsa_circ_154727,RMVar_hsa_circ_154726,RMVar_hsa_circ_68152 34585 RMVar_ID_34585 Human_SNP_ID_489868988 A-to-I Human chr12 - 7929562 7929562 7929562 TACTCAGGAGGCTGAGGTAAGAGGATCACTTGAGCTCAGGAGTTTCAGGTTGCAGTGAGCTATAA TACTCAGGAGGCTGAGGTAAGAGGATCACTTGCGCTCAGGAGTTTCAGGTTGCAGTGAGCTATAA T G SLC2A3 Ensembl:ENSG00000059804 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs112237103 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124122,RMVar_hsa_circ_95032,RMVar_hsa_circ_154727,RMVar_hsa_circ_154726,RMVar_hsa_circ_68152 34586 RMVar_ID_34586 Human_SNP_ID_489868991 A-to-I Human chr12 - 7929567 7929567 7929567 CCAGCTACTCAGGAGGCTGAGGTAAGAGGATCACTTGAGCTCAGGAGTTTCAGGTTGCAGTGAGC CCAGCTACTCAGGAGGCTGAGGTAAGAGGATCGCTTGAGCTCAGGAGTTTCAGGTTGCAGTGAGC T C SLC2A3 Ensembl:ENSG00000059804 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1308914573 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124122,RMVar_hsa_circ_95032,RMVar_hsa_circ_154727,RMVar_hsa_circ_154726,RMVar_hsa_circ_68152 34587 RMVar_ID_34587 Human_SNP_ID_489868992 A-to-I Human chr12 - 7929576 7929570 7929577 TCTGTAGTCCCAGCTACTCAGGAGGCTGAGGTAAGAGGATCACTTGAGCTCAGGAGTTTCAGGTT TCTGTAGTCCCAGCTACTCAGGAGGCTGAGG_______ATCACTTGAGCTCAGGAGTTTCAGGTT TCCTCTTA T SLC2A3 Ensembl:ENSG00000059804 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1055286686 Functional Loss DEL dbSNP153 32..38 33 - - - RMVar_hsa_circ_124122,RMVar_hsa_circ_95032,RMVar_hsa_circ_154727,RMVar_hsa_circ_154726,RMVar_hsa_circ_68152 34588 RMVar_ID_34588 Human_SNP_ID_489879838 A-to-I Human chr12 - 7964078 7964078 7964078 GAACTCCTGATCTCAGGTTATCCACCCGCCTCAGCCTCTCCAAGTGCTGGGATTACAAGTGTGAG GAACTCCTGATCTCAGGTTATCCACCCGCCTCGGCCTCTCCAAGTGCTGGGATTACAAGTGTGAG T C lnc-SLC2A3-4,lnc-SLC2A3-4:2,lnc-SLC2A3-4:3,lnc-SLC2A3-4:4 RNACentral:URS0000D58CF2,RNACentral:URS0000D5C301,RNACentral:URS0000E5BAED,RNACentral:URS0000D57A1B lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,exon GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1015652047 Functional Loss SNV dbSNP153 33..33 33 - - - 34589 RMVar_ID_34589 Human_SNP_ID_489879897 A-to-I Human chr12 - 7964269 7964269 7964269 TCGAGCTGTCGCCCAGGCTGGAGTGCAATGGCATGATCTTGGCTCACTGCAACCTCTGCCTCCCG TCGAGCTGTCGCCCAGGCTGGAGTGCAATGGCGTGATCTTGGCTCACTGCAACCTCTGCCTCCCG T C lnc-SLC2A3-4,lnc-SLC2A3-4:2,lnc-SLC2A3-4:3,lnc-SLC2A3-4:4 RNACentral:URS0000D58CF2,RNACentral:URS0000D5C301,RNACentral:URS0000E5BAED,RNACentral:URS0000D57A1B lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1309300029 Functional Loss SNV dbSNP153 33..33 33 - - - 34590 RMVar_ID_34590 Human_SNP_ID_489879899 A-to-I Human chr12 - 7964274 7964274 7964274 GAGTATCGAGCTGTCGCCCAGGCTGGAGTGCAATGGCATGATCTTGGCTCACTGCAACCTCTGCC GAGTATCGAGCTGTCGCCCAGGCTGGAGTGCAGTGGCATGATCTTGGCTCACTGCAACCTCTGCC T C lnc-SLC2A3-4,lnc-SLC2A3-4:2,lnc-SLC2A3-4:3,lnc-SLC2A3-4:4 RNACentral:URS0000D58CF2,RNACentral:URS0000D5C301,RNACentral:URS0000E5BAED,RNACentral:URS0000D57A1B lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1324523510 Functional Loss SNV dbSNP153 33..33 33 - - - 34591 RMVar_ID_34591 Human_SNP_ID_489880610 A-to-I Human chr12 - 7966625 7966625 7966625 TATTTTCAGTAGAGATGGGGTTTCACCACGTTAGCCAGGCTGGTCTCGAACTCCTGACCTCGTGA TATTTTCAGTAGAGATGGGGTTTCACCACGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCGTGA T C lnc-SLC2A3-4,lnc-SLC2A3-4:2,lnc-SLC2A3-4:3,lnc-SLC2A3-4:4 RNACentral:URS0000D58CF2,RNACentral:URS0000D5C301,RNACentral:URS0000E5BAED,RNACentral:URS0000D57A1B lincRNA,lincRNA,lincRNA,lincRNA exon,intron,exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1418617316 Functional Loss SNV dbSNP153 33..33 33 - - - 34592 RMVar_ID_34592 Human_SNP_ID_489913802 A-to-I Human chr12 + 8093556 8093556 8093556 TGAGATCAGCCTGGGCAACATGATGAAATCCCATCTCTACAAAAAAAATACAAACATTAGTTGGA TGAGATCAGCCTGGGCAACATGATGAAATCCCGTCTCTACAAAAAAAATACAAACATTAGTTGGA A G NECAP1,AC006511.6 Ensembl:ENSG00000089818,Ensembl:ENSG00000284697 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1465505725 Functional Loss SNV dbSNP153 33..33 33 - - - 34593 RMVar_ID_34593 Human_SNP_ID_489944012 A-to-I Human chr12 + 8215931 8215931 8215931 CCAACCCTTTGGGAGGTCAAAGCAAGCAGATCACGAGATCAGGAAACTGAGACCATCCTAGCCAA CCAACCCTTTGGGAGGTCAAAGCAAGCAGATCGCGAGATCAGGAAACTGAGACCATCCTAGCCAA A G FAM66C Ensembl:ENSG00000226711 lincRNA exon GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1248415989 Functional Loss SNV dbSNP153 33..33 33 - - - 34594 RMVar_ID_34594 Human_SNP_ID_489948054 A-to-I Human chr12 - 8226067 8226067 8226067 CTTAGAGTGGGCTGTGCAGATAGACCTTTCCGAGTCATGTAATTGGATTAAGTTAATTGTAATTA CTTAGAGTGGGCTGTGCAGATAGACCTTTCCGGGTCATGTAATTGGATTAAGTTAATTGTAATTA T C FAM90A1 Ensembl:ENSG00000171847 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs796442698 Functional Loss SNV dbSNP153 33..33 33 - - - 34595 RMVar_ID_34595 Human_SNP_ID_490028344 A-to-I Human chr12 + 8512413 8512413 8512413 AGCTGTGTCTTTGGATTTGTAGGCCACTCCTCAACTTTTCAGCTCCCGCACGATTCCTTAGGGCA AGCTGTGTCTTTGGATTTGTAGGCCACTCCTCGACTTTTCAGCTCCCGCACGATTCCTTAGGGCA A G CLEC4D Ensembl:ENSG00000166527 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1310836462 Functional Loss SNV dbSNP153 33..33 33 - - - 34596 RMVar_ID_34596 Human_SNP_ID_490028353 A-to-I Human chr12 + 8512440 8512440 8512440 TCCTCAACTTTTCAGCTCCCGCACGATTCCTTAGGGCAAGCGACCAGTGGTTGACACCGCATATA TCCTCAACTTTTCAGCTCCCGCACGATTCCTTGGGGCAAGCGACCAGTGGTTGACACCGCATATA A G CLEC4D Ensembl:ENSG00000166527 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1190477680 Functional Loss SNV dbSNP153 33..33 33 - - - 34597 RMVar_ID_34597 Human_SNP_ID_490035474 A-to-I Human chr12 - 8540794 8540794 8540794 AGAAACAAAAAACCAAAGAGAGAGAAAAAATGAATTCATCTAAATCATCTGAAACACAATGCACA AGAAACAAAAAACCAAAGAGAGAGAAAAAATGCATTCATCTAAATCATCTGAAACACAATGCACA T G CLEC4E Ensembl:ENSG00000166523 Protein coding CDS GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs749293813 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1336159,Human_Splice_Rec_1336169,Human_Splice_Rec_1336175,Human_Splice_Rec_1336187,Human_Splice_Rec_1336195 34598 RMVar_ID_34598 Human_SNP_ID_490076598 A-to-I Human chr12 + 8703688 8703688 8703688 GCAATCCTTTTGCTTCAGACTCCCAAAGTACTAGGATTACAGGTGTGAATCACTGTGCCTGGCCC GCAATCCTTTTGCTTCAGACTCCCAAAGTACTGGGATTACAGGTGTGAATCACTGTGCCTGGCCC A G RIMKLB Ensembl:ENSG00000166532 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs776315390 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98066,RMVar_hsa_circ_32635,RMVar_hsa_circ_154751,RMVar_hsa_circ_374467,RMVar_hsa_circ_154752 34599 RMVar_ID_34599 Human_SNP_ID_490078500 A-to-I Human chr12 + 8710488 8710488 8710488 TACTGCCACACCTGGCTCATTTTTGTATTTTTAGTAAAGACAGGGTTTTGCCATATTGGCCAGGC TACTGCCACACCTGGCTCATTTTTGTATTTTTGGTAAAGACAGGGTTTTGCCATATTGGCCAGGC A G RIMKLB Ensembl:ENSG00000166532 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1402624420 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98066,RMVar_hsa_circ_32635,RMVar_hsa_circ_154751,RMVar_hsa_circ_374467,RMVar_hsa_circ_154752 34600 RMVar_ID_34600 Human_SNP_ID_490080685 A-to-I Human chr12 + 8718536 8718536 8718536 CTGGTGGCATGCGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGTCAGGAGAATCGATTGAACCCC CTGGTGGCATGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGTCAGGAGAATCGATTGAACCCC A G RIMKLB Ensembl:ENSG00000166532 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1473113184 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5505,RMVar_hsa_circ_76282,RMVar_hsa_circ_374467,RMVar_hsa_circ_283026,RMVar_hsa_circ_154752,RMVar_hsa_circ_154755,RMVar_hsa_circ_154756,RMVar_hsa_circ_154754 34601 RMVar_ID_34601 Human_SNP_ID_490084899 A-to-I Human chr12 + 8733790 8733790 8733790 CTGTAGTCCTAGCTACTCGGAGAGGCTGAGGTAGGAGGATTGATTGAGCACAGGAATTGGAGGCT CTGTAGTCCTAGCTACTCGGAGAGGCTGAGGTGGGAGGATTGATTGAGCACAGGAATTGGAGGCT A G RIMKLB Ensembl:ENSG00000166532 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1416903304 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5505,RMVar_hsa_circ_76282,RMVar_hsa_circ_374467,RMVar_hsa_circ_283026,RMVar_hsa_circ_154752,RMVar_hsa_circ_154755,RMVar_hsa_circ_154756 34602 RMVar_ID_34602 Human_SNP_ID_490088201 A-to-I Human chr12 + 8746853 8746853 8746853 GTCTTAAACTCCTGGGCTCAAATTATCCTCCTACCTCAGCCTTCTGAGTAACTAGGGCTACAGAC GTCTTAAACTCCTGGGCTCAAATTATCCTCCTGCCTCAGCCTTCTGAGTAACTAGGGCTACAGAC A G RIMKLB Ensembl:ENSG00000166532 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935691935 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5505,RMVar_hsa_circ_76282,RMVar_hsa_circ_374467,RMVar_hsa_circ_283026,RMVar_hsa_circ_154752,RMVar_hsa_circ_154755,RMVar_hsa_circ_154756 34603 RMVar_ID_34603 Human_SNP_ID_490088206 A-to-I Human chr12 + 8746874 8746874 8746874 ATTATCCTCCTACCTCAGCCTTCTGAGTAACTAGGGCTACAGACACACACAACCACACCTGGCTA ATTATCCTCCTACCTCAGCCTTCTGAGTAACTGGGGCTACAGACACACACAACCACACCTGGCTA A G RIMKLB Ensembl:ENSG00000166532 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1455585958 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5505,RMVar_hsa_circ_76282,RMVar_hsa_circ_374467,RMVar_hsa_circ_283026,RMVar_hsa_circ_154752,RMVar_hsa_circ_154755,RMVar_hsa_circ_154756 34604 RMVar_ID_34604 Human_SNP_ID_490191782 A-to-I Human chr12 + 9162162 9162162 9162162 TTTTGTTTTTTTCGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGTTCTCAAACCCCTGACCT TTTTGTTTTTTTCGTAGAGACAGGGTTTCACCGTGTTGGCCAGGCTGTTCTCAAACCCCTGACCT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1358471767 Functional Loss SNV dbSNP153 33..33 33 - - - 34605 RMVar_ID_34605 Human_SNP_ID_490199597 A-to-I Human chr12 + 9195523 9195506 9195524 TGGAGTGCAGTGGTGCCATTATAACTCACAGCAGCATCGAAGTTCTGGGCTCGAGGGATCCTCCC TGGAGTGCAGTGGTGC__________________CATCGAAGTTCTGGGCTCGAGGGATCCTCCC CCATTATAACTCACAGCAG C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1201253359 Functional Loss DEL dbSNP153 17..34 33 - - - 34606 RMVar_ID_34606 Human_SNP_ID_490205322 A-to-I Human chr12 + 9219502 9219501 9219502 CAAGATGGATTAAAGACCTAAATGTAAAACCTAAAACTATAAAATCCTGGAAGATAACCTAGAAA CAAGATGGATTAAAGACCTAAATGTAAAACCT_AAACTATAAAATCCTGGAAGATAACCTAGAAA TA T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1420946112 Functional Loss DEL dbSNP153 33..33 33 - - - 34607 RMVar_ID_34607 Human_SNP_ID_490263502 A-to-I Human chr12 - 9427867 9427867 9427867 CACCATTGTGACCTATTTCCATTCTCTTTTTTAGGGAACATTAAGCAAAATCCCAATACACAGAG CACCATTGTGACCTATTTCCATTCTCTTTTTTGGGGAACATTAAGCAAAATCCCAATACACAGAG T C DDX12P Ensembl:ENSG00000214826 Pseudogene intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1199939753 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17358375 Human_Splice_Rec_1337673 34608 RMVar_ID_34608 Human_SNP_ID_490313546 A-to-I Human chr12 + 9658756 9658756 9658756 CTAAAAACACAAAATTAGCCAGGCATCGTGGCACACGCCTGTAGTCCCAGCTACTCGAGAGGCTG CTAAAAACACAAAATTAGCCAGGCATCGTGGCGCACGCCTGTAGTCCCAGCTACTCGAGAGGCTG A G AC010186.3 Ensembl:ENSG00000257027 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10771996 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_154848 34609 RMVar_ID_34609 Human_SNP_ID_490313547 A-to-I Human chr12 + 9658756 9658756 9658756 CTAAAAACACAAAATTAGCCAGGCATCGTGGCACACGCCTGTAGTCCCAGCTACTCGAGAGGCTG CTAAAAACACAAAATTAGCCAGGCATCGTGGCTCACGCCTGTAGTCCCAGCTACTCGAGAGGCTG A T AC010186.3 Ensembl:ENSG00000257027 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10771996 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_154848 34610 RMVar_ID_34610 Human_SNP_ID_490313706 A-to-I Human chr12 + 9659352 9659352 9659352 GGGACATTAGATACCAGAATTGGGAACAAACTAGATCCATAAGATACTATGGTCAGTAATGAGAT GGGACATTAGATACCAGAATTGGGAACAAACTGGATCCATAAGATACTATGGTCAGTAATGAGAT A G AC010186.3 Ensembl:ENSG00000257027 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11052241 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_3863 RMVar_hsa_circ_154848 34611 RMVar_ID_34611 Human_SNP_ID_490313731 A-to-I Human chr12 + 9659428 9659424 9659428 GTGACTTTTTTTTTTTTTTTAAATGGAGTCTCACTCTGTCACCCAGAGTGGAGTGCAGTGGCATG GTGACTTTTTTTTTTTTTTTAAATGGAGT____CTCTGTCACCCAGAGTGGAGTGCAGTGGCATG TCTCA T AC010186.3 Ensembl:ENSG00000257027 lincRNA intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1382602271 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_154848 34612 RMVar_ID_34612 Human_SNP_ID_490313732 A-to-I Human chr12 + 9659428 9659428 9659428 GTGACTTTTTTTTTTTTTTTAAATGGAGTCTCACTCTGTCACCCAGAGTGGAGTGCAGTGGCATG GTGACTTTTTTTTTTTTTTTAAATGGAGTCTCTCTCTGTCACCCAGAGTGGAGTGCAGTGGCATG A T AC010186.3 Ensembl:ENSG00000257027 lincRNA intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs568219089 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_154848 34613 RMVar_ID_34613 Human_SNP_ID_490320832 A-to-I Human chr12 + 9688659 9688659 9688659 CAGAATTGCTTGAACCTGGGAGGTGGAGGCCTACAGTTAGCTGAAATCATGCTACTGTACTCCAG CAGAATTGCTTGAACCTGGGAGGTGGAGGCCTGCAGTTAGCTGAAATCATGCTACTGTACTCCAG A G CLEC2D Ensembl:ENSG00000069493 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1306772274 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18635398,Human_RBP_ID_25013975 RMVar_hsa_circ_154848,RMVar_hsa_circ_154849,RMVar_hsa_circ_154850 34614 RMVar_ID_34614 Human_SNP_ID_490320833 A-to-I Human chr12 + 9688661 9688661 9688661 GAATTGCTTGAACCTGGGAGGTGGAGGCCTACAGTTAGCTGAAATCATGCTACTGTACTCCAGCC GAATTGCTTGAACCTGGGAGGTGGAGGCCTACCGTTAGCTGAAATCATGCTACTGTACTCCAGCC A C CLEC2D Ensembl:ENSG00000069493 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs754761061 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18635398,Human_RBP_ID_25013975 RMVar_hsa_circ_154848,RMVar_hsa_circ_154849,RMVar_hsa_circ_154850 34615 RMVar_ID_34615 Human_SNP_ID_490321683 A-to-I Human chr12 + 9692253 9692253 9692253 TGTCTCCCAGGTTCAAATGATTCTCATGCCTCAGCCTCCCAAATAGCTGGGATTACAGGTGCATG TGTCTCCCAGGTTCAAATGATTCTCATGCCTCCGCCTCCCAAATAGCTGGGATTACAGGTGCATG A C CLEC2D Ensembl:ENSG00000069493 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1226377919 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_154848,RMVar_hsa_circ_154849,RMVar_hsa_circ_154850 34616 RMVar_ID_34616 Human_SNP_ID_490360937 A-to-I Human chr12 - 9857785 9857784 9857786 TACTGTCATTTGACCTAACATGACAAAGACATAAAATTTTTTCAACTTATCATATAATAGATATA TACTGTCATTTGACCTAACATGACAAAGACA__AAATTTTTTCAACTTATCATATAATAGATATA TTA T CLEC2B Ensembl:ENSG00000110852 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1284299419 Functional Loss DEL dbSNP153 32..33 33 - - - 34617 RMVar_ID_34617 Human_SNP_ID_646136925 A-to-I Human chr18 + 45831837 45831837 45831837 TCGGCTCACTGCAGCCTCCGCCTCCCGGGTTCAAGCGGTTCTCCTGCCTCAGCCTCCTGAGTGGC TCGGCTCACTGCAGCCTCCGCCTCCCGGGTTCCAGCGGTTCTCCTGCCTCAGCCTCCTGAGTGGC A C SIGLEC15 Ensembl:ENSG00000197046 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1473721920 Functional Loss SNV dbSNP153 33..33 33 - - - 34618 RMVar_ID_34618 Human_SNP_ID_646145871 A-to-I Human chr18 - 45868572 45868572 45868572 CTGAGGCTGGGGGTTCAAGACCAGCCTGACCAACATGGAGAAACCCGGACTCTACTAAAAATAAA CTGAGGCTGGGGGTTCAAGACCAGCCTGACCAGCATGGAGAAACCCGGACTCTACTAAAAATAAA T C EPG5 Ensembl:ENSG00000152223 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1310676922 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25349,RMVar_hsa_circ_97827,RMVar_hsa_circ_368591,RMVar_hsa_circ_105392,RMVar_hsa_circ_95005,RMVar_hsa_circ_96486,RMVar_hsa_circ_5038,RMVar_hsa_circ_51140,RMVar_hsa_circ_189833,RMVar_hsa_circ_189835,RMVar_hsa_circ_21350,RMVar_hsa_circ_189836,RMVar_hsa_circ_189834,RMVar_hsa_circ_91815,RMVar_hsa_circ_102315,RMVar_hsa_circ_119019,RMVar_hsa_circ_31920,RMVar_hsa_circ_189838,RMVar_hsa_circ_189840,RMVar_hsa_circ_114484,RMVar_hsa_circ_189839,RMVar_hsa_circ_98759,RMVar_hsa_circ_189844,RMVar_hsa_circ_100625,RMVar_hsa_circ_189841,RMVar_hsa_circ_189842,RMVar_hsa_circ_189843,RMVar_hsa_circ_308689,RMVar_hsa_circ_189846,RMVar_hsa_circ_124815,RMVar_hsa_circ_311587,RMVar_hsa_circ_189845 34619 RMVar_ID_34619 Human_SNP_ID_646166438 A-to-I Human chr18 - 45953631 45953631 45953631 CTCAAGTTTGAGAGGGGATGGAGAAGACCATTAGATGCAACCCTATGGAGGCCAAAGTGATCATA CTCAAGTTTGAGAGGGGATGGAGAAGACCATTGGATGCAACCCTATGGAGGCCAAAGTGATCATA T C EPG5 Ensembl:ENSG00000152223 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs915767641 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21350,RMVar_hsa_circ_115268,RMVar_hsa_circ_189871,RMVar_hsa_circ_36696,RMVar_hsa_circ_56507 34620 RMVar_ID_34620 Human_SNP_ID_646195783 A-to-I Human chr18 - 46076436 46076436 46076436 GCTGGTCTCGAACTTCTGATCTCAAATGATCCACCCACCTCAGCCTCCCAAAGTGCTGGGATTAC GCTGGTCTCGAACTTCTGATCTCAAATGATCCGCCCACCTCAGCCTCCCAAAGTGCTGGGATTAC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1395112273 Functional Loss SNV dbSNP153 33..33 33 - - - 34621 RMVar_ID_34621 Human_SNP_ID_646196975 A-to-I Human chr18 - 46080938 46080938 46080938 TTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGGTTTCGAACTCCTGACCTTAGATGATC TTTAGTAGAGACGGGGTTTCACCATGTTGGCCGGGCTGGTTTCGAACTCCTGACCTTAGATGATC T C ATP5F1A Ensembl:ENSG00000152234 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1192473957 Functional Loss SNV dbSNP153 33..33 33 - - - 34622 RMVar_ID_34622 Human_SNP_ID_646202037 A-to-I Human chr18 - 46096907 46096907 46096907 GTGATCTCCGCCCACTGCAACCACCGCCTCCCAGGATCAAGTGATTCTCCCACCTCAGCCTCCCG GTGATCTCCGCCCACTGCAACCACCGCCTCCCGGGATCAAGTGATTCTCCCACCTCAGCCTCCCG T C ATP5F1A Ensembl:ENSG00000152234 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs556706885 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120046,RMVar_hsa_circ_189882,RMVar_hsa_circ_76524,RMVar_hsa_circ_189901 34623 RMVar_ID_34623 Human_SNP_ID_646203884 A-to-I Human chr18 - 46102910 46102910 46102910 ACAGGGTCTTGCTCTTTCGTCCAAGCTGGAGTATAGTGGTGATCACAGTTCACTGCAACCTTGAA ACAGGGTCTTGCTCTTTCGTCCAAGCTGGAGTGTAGTGGTGATCACAGTTCACTGCAACCTTGAA T C ATP5F1A Ensembl:ENSG00000152234 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1423863734 Functional Loss SNV dbSNP153 33..33 33 - - - 34624 RMVar_ID_34624 Human_SNP_ID_646204774 A-to-I Human chr18 + 46105761 46105761 46105761 GCACCACCACACCCGGCTAATTTTTGTGTTTTAGTAAAGACAGGGTTTCACAATATTGGCCAGGC GCACCACCACACCCGGCTAATTTTTGTGTTTTGGTAAAGACAGGGTTTCACAATATTGGCCAGGC A G HAUS1 Ensembl:ENSG00000152240 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs890296265 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82962,RMVar_hsa_circ_109823,RMVar_hsa_circ_189905,RMVar_hsa_circ_189906,RMVar_hsa_circ_77365,RMVar_hsa_circ_189907 34625 RMVar_ID_34625 Human_SNP_ID_646206196 A-to-I Human chr18 + 46110976 46110976 46110976 TCGGCTCACTGCAACCTCTGCCTTCCGGATTCAAGCGATTCTCGTGCCTCAGCCTCCTGGGTAGC TCGGCTCACTGCAACCTCTGCCTTCCGGATTCGAGCGATTCTCGTGCCTCAGCCTCCTGGGTAGC A G HAUS1 Ensembl:ENSG00000152240 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005838297 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82962,RMVar_hsa_circ_109823,RMVar_hsa_circ_7367,RMVar_hsa_circ_189905,RMVar_hsa_circ_189906,RMVar_hsa_circ_77365,RMVar_hsa_circ_189907 34626 RMVar_ID_34626 Human_SNP_ID_646206230 A-to-I Human chr18 + 46111083 46111083 46111083 TATTTTTAGTAGAAACAGGGTTTCTCCGTGTTAGCCAGAATGGTCTTGATCTCCTGATCCATCCA TATTTTTAGTAGAAACAGGGTTTCTCCGTGTTGGCCAGAATGGTCTTGATCTCCTGATCCATCCA A G HAUS1 Ensembl:ENSG00000152240 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1398588366 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82962,RMVar_hsa_circ_109823,RMVar_hsa_circ_7367,RMVar_hsa_circ_189905,RMVar_hsa_circ_189906,RMVar_hsa_circ_77365,RMVar_hsa_circ_189907 34627 RMVar_ID_34627 Human_SNP_ID_646223186 A-to-I Human chr18 + 46177788 46177788 46177788 AAACTTAGCTGGGTGGGGTGGTATGCATCTTTAGTCCCTGCTGCTTGTGGGGCTGAGGTGGAAGG AAACTTAGCTGGGTGGGGTGGTATGCATCTTTTGTCCCTGCTGCTTGTGGGGCTGAGGTGGAAGG A T C18orf25 Ensembl:ENSG00000152242 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs996600806 Functional Loss SNV dbSNP153 33..33 33 - - - 34628 RMVar_ID_34628 Human_SNP_ID_646224893 A-to-I Human chr18 + 46184637 46184637 46184637 CCAGCTACTCAGGAAGCTGAGGTGGGAGAATCACCTGAGCCTAGGAAGGTAAGGCTGCAATGAGC CCAGCTACTCAGGAAGCTGAGGTGGGAGAATCGCCTGAGCCTAGGAAGGTAAGGCTGCAATGAGC A G C18orf25 Ensembl:ENSG00000152242 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1334744379 Functional Loss SNV dbSNP153 33..33 33 - - - 34629 RMVar_ID_34629 Human_SNP_ID_646225295 A-to-I Human chr18 + 46186220 46186220 46186220 TGATTATCATGAATTTTTTTTTTTTTTGAGACAAAGTCTTGCTCTGTCGCCAGGCTGGAGTGCAG TGATTATCATGAATTTTTTTTTTTTTTGAGACGAAGTCTTGCTCTGTCGCCAGGCTGGAGTGCAG A G C18orf25 Ensembl:ENSG00000152242 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1272347322 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_136415 34630 RMVar_ID_34630 Human_SNP_ID_646227041 A-to-I Human chr18 + 46192660 46192660 46192660 GTGATCTCGTCTCACTGCATTCTCTGCCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGTCTCCCA GTGATCTCGTCTCACTGCATTCTCTGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGTCTCCCA A G C18orf25 Ensembl:ENSG00000152242 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1169953139 Functional Loss SNV dbSNP153 33..33 33 - - - 34631 RMVar_ID_34631 Human_SNP_ID_646227148 A-to-I Human chr18 + 46193043 46193043 46193043 AATAGTGAAACTGGGCATGGTGGCACGTTCCTATAGTCCCAGCTACTTGGGAGACTGAGGCAGGA AATAGTGAAACTGGGCATGGTGGCACGTTCCTGTAGTCCCAGCTACTTGGGAGACTGAGGCAGGA A G C18orf25 Ensembl:ENSG00000152242 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs143367459 Functional Loss SNV dbSNP153 33..33 33 - - - 34632 RMVar_ID_34632 Human_SNP_ID_646227380 A-to-I Human chr18 + 46193833 46193832 46193833 GTTGGCCAGACTGGTCTTGAACTCCTGGCCTCAAGTGATCTGCCCACCTTGGCCTCCCAAAGTGC GTTGGCCAGACTGGTCTTGAACTCCTGGCCTC_AGTGATCTGCCCACCTTGGCCTCCCAAAGTGC CA C C18orf25 Ensembl:ENSG00000152242 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1209646196 Functional Loss DEL dbSNP153 33..33 33 - - - 34633 RMVar_ID_34633 Human_SNP_ID_646227381 A-to-I Human chr18 + 46193833 46193833 46193833 GTTGGCCAGACTGGTCTTGAACTCCTGGCCTCAAGTGATCTGCCCACCTTGGCCTCCCAAAGTGC GTTGGCCAGACTGGTCTTGAACTCCTGGCCTCGAGTGATCTGCCCACCTTGGCCTCCCAAAGTGC A G C18orf25 Ensembl:ENSG00000152242 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs533086777 Functional Loss SNV dbSNP153 33..33 33 - - - 34634 RMVar_ID_34634 Human_SNP_ID_646229825 A-to-I Human chr18 + 46202360 46202360 46202360 GAAAAGTGTCCTACTAGCACCCATGTACTTGTAGCATAGAAAAGGCATTCAACATAGGAAAGGCA GAAAAGTGTCCTACTAGCACCCATGTACTTGTGGCATAGAAAAGGCATTCAACATAGGAAAGGCA A G C18orf25 Ensembl:ENSG00000152242 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1306155436 Functional Loss SNV dbSNP153 33..33 33 - - - 34635 RMVar_ID_34635 Human_SNP_ID_646229907 A-to-I Human chr18 + 46202677 46202677 46202677 GGGCGTAGTGGCGGGTGCCTGTAATCCCGGCTACTCAGAAGGCTGAAGGAGGAGAATCGCTTGAA GGGCGTAGTGGCGGGTGCCTGTAATCCCGGCTGCTCAGAAGGCTGAAGGAGGAGAATCGCTTGAA A G C18orf25 Ensembl:ENSG00000152242 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1452501059 Functional Loss SNV dbSNP153 33..33 33 - - - 34636 RMVar_ID_34636 Human_SNP_ID_646229908 A-to-I Human chr18 + 46202677 46202677 46202677 GGGCGTAGTGGCGGGTGCCTGTAATCCCGGCTACTCAGAAGGCTGAAGGAGGAGAATCGCTTGAA GGGCGTAGTGGCGGGTGCCTGTAATCCCGGCTTCTCAGAAGGCTGAAGGAGGAGAATCGCTTGAA A T C18orf25 Ensembl:ENSG00000152242 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1452501059 Functional Loss SNV dbSNP153 33..33 33 - - - 34637 RMVar_ID_34637 Human_SNP_ID_646234081 A-to-I Human chr18 + 46219743 46219743 46219743 CCGCTTGCCTTGGCCTCCCAAGTGCTGTGATTACAGGTGTGAGCCACCACGCCCGGCCATTATCA CCGCTTGCCTTGGCCTCCCAAGTGCTGTGATTGCAGGTGTGAGCCACCACGCCCGGCCATTATCA A G C18orf25 Ensembl:ENSG00000152242 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1415927605 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39335,RMVar_hsa_circ_60061 34638 RMVar_ID_34638 Human_SNP_ID_646234469 A-to-I Human chr18 + 46221449 46221449 46221449 GGGTGTGGTGGCGCGCGTCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAA GGGTGTGGTGGCGCGCGTCTGTAGTCCCAGCTGCTCGGGAGGCTGAGGCAGGAGAATCACTTGAA A G C18orf25 Ensembl:ENSG00000152242 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1007283145 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39335,RMVar_hsa_circ_60061 34639 RMVar_ID_34639 Human_SNP_ID_646235863 A-to-I Human chr18 + 46227677 46227677 46227677 TGGAATGCAATGGCACGAACCCGACTCACTGCAACTTCCGCCTCCCAGGTTCAAGTGATTCTCCT TGGAATGCAATGGCACGAACCCGACTCACTGCCACTTCCGCCTCCCAGGTTCAAGTGATTCTCCT A C C18orf25 Ensembl:ENSG00000152242 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs911315725 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13314003 RMVar_hsa_circ_39335,RMVar_hsa_circ_60061 34640 RMVar_ID_34640 Human_SNP_ID_646383240 A-to-I Human chr18 - 46824752 46824752 46824752 GCCATCCACCTGTCTTGGCCTGCCAAAGTGCTAGGATTACAAAATGCATAAGCCACCACGCCTGG GCCATCCACCTGTCTTGGCCTGCCAAAGTGCTGGGATTACAAAATGCATAAGCCACCACGCCTGG T C PIAS2 Ensembl:ENSG00000078043 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1417297973 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22964088 RMVar_hsa_circ_51537,RMVar_hsa_circ_189938,RMVar_hsa_circ_323241,RMVar_hsa_circ_361058,RMVar_hsa_circ_351253,RMVar_hsa_circ_323124,RMVar_hsa_circ_88083,RMVar_hsa_circ_280687,RMVar_hsa_circ_189940,RMVar_hsa_circ_189939,RMVar_hsa_circ_189936,RMVar_hsa_circ_189937,RMVar_hsa_circ_189935,RMVar_hsa_circ_189943,RMVar_hsa_circ_370150,RMVar_hsa_circ_322903 34641 RMVar_ID_34641 Human_SNP_ID_646402874 A-to-I Human chr18 - 46904840 46904840 46904840 TAATCCTGTAATCTTAGCACCTTGGGAGGCTGAGGTGGGAGGATCACTTGAGCCCAAGAGTTTGA TAATCCTGTAATCTTAGCACCTTGGGAGGCTGTGGTGGGAGGATCACTTGAGCCCAAGAGTTTGA T A PIAS2 Ensembl:ENSG00000078043 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs905030868 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41169,RMVar_hsa_circ_88083,RMVar_hsa_circ_189935,RMVar_hsa_circ_46556,RMVar_hsa_circ_311508,RMVar_hsa_circ_189959 34642 RMVar_ID_34642 Human_SNP_ID_646406619 A-to-I Human chr18 + 46919073 46919073 46919073 TATACACAACACACACACATATTGTTTTGGCCAGGTGCAGTGGCTCATGCCTGTAATCCCAGCAC TATACACAACACACACACATATTGTTTTGGCCCGGTGCAGTGGCTCATGCCTGTAATCCCAGCAC A C KATNAL2 Ensembl:ENSG00000167216 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs923792188 Functional Loss SNV dbSNP153 33..33 33 - - - 34643 RMVar_ID_34643 Human_SNP_ID_646415456 A-to-I Human chr18 + 46953712 46953712 46953712 CCGGCAGGTTGAGGCTGCAGTGAGCCGTGATCACACCACTGTACTCCAACCTAGGCGACACATGG CCGGCAGGTTGAGGCTGCAGTGAGCCGTGATCGCACCACTGTACTCCAACCTAGGCGACACATGG A G KATNAL2 Ensembl:ENSG00000167216 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs966195584 Functional Loss SNV dbSNP153 33..33 33 - - - 34644 RMVar_ID_34644 Human_SNP_ID_646437990 A-to-I Human chr18 - 47096539 47096539 47096539 GTAGAAGATTCGCTGACTATGCTGGGCAACATAGTGAGACCCCGTCTCTGCACAATATAAAAATT GTAGAAGATTCGCTGACTATGCTGGGCAACATGGTGAGACCCCGTCTCTGCACAATATAAAAATT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1047045961 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_189969 34645 RMVar_ID_34645 Human_SNP_ID_646448808 A-to-I Human chr18 - 47140576 47140576 47140576 CAGTCGAGGCTGCAGTGAGCTGTGATCATGCAACTGCACTCCAGCCTGGGTGACAGAACAAGGCC CAGTCGAGGCTGCAGTGAGCTGTGATCATGCAGCTGCACTCCAGCCTGGGTGACAGAACAAGGCC T C AC012254.2,HDHD2 Ensembl:ENSG00000267228,Ensembl:ENSG00000167220 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs866218855 Functional Loss SNV dbSNP153 33..33 33 - - - 34646 RMVar_ID_34646 Human_SNP_ID_646448818 A-to-I Human chr18 - 47140616 47140616 47140616 TACTTGGGAGGCCGATGTGAGAGGATTGCTTGAGCATGGGCAGTCGAGGCTGCAGTGAGCTGTGA TACTTGGGAGGCCGATGTGAGAGGATTGCTTGGGCATGGGCAGTCGAGGCTGCAGTGAGCTGTGA T C AC012254.2,HDHD2 Ensembl:ENSG00000267228,Ensembl:ENSG00000167220 Protein coding,Protein coding intron,intron GSE100210;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229 RNA-Seq:(High) rs918738214 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13316024 34647 RMVar_ID_34647 Human_SNP_ID_646449419 A-to-I Human chr18 - 47143230 47143230 47143230 CCAGGCTGGTCTCGAACTCCTGGATTCAAGCAATCCTCCTACCTCAGCCACCCAAAGTGCTGGGA CCAGGCTGGTCTCGAACTCCTGGATTCAAGCAGTCCTCCTACCTCAGCCACCCAAAGTGCTGGGA T C AC012254.2,HDHD2 Ensembl:ENSG00000267228,Ensembl:ENSG00000167220 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs545158153 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9898758 34648 RMVar_ID_34648 Human_SNP_ID_646449772 A-to-I Human chr18 - 47144683 47144683 47144683 CAGTCCCTCCCACCTTAGCCTCCCAAGTAGCTAGGACTACAGGCCCATGCTACCACGCTTGGCTA CAGTCCCTCCCACCTTAGCCTCCCAAGTAGCTGGGACTACAGGCCCATGCTACCACGCTTGGCTA T C AC012254.2,HDHD2 Ensembl:ENSG00000267228,Ensembl:ENSG00000167220 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924207440 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6689390 34649 RMVar_ID_34649 Human_SNP_ID_646619629 A-to-I Human chr18 - 47822750 47822750 47822750 GCTTGAACCCTGGAGGCAGAAGTTGCACTGAAACAAGATCGTGCCACTGCATTCCAGCTGGGGCA GCTTGAACCCTGGAGGCAGAAGTTGCACTGAAGCAAGATCGTGCCACTGCATTCCAGCTGGGGCA T C SMAD2 Ensembl:ENSG00000175387 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs933885823 Functional Loss SNV dbSNP153 33..33 33 - - - 34650 RMVar_ID_34650 Human_SNP_ID_646631156 A-to-I Human chr18 - 47860125 47860125 47860125 TTTAAGTCATAGGATTGATTAATTGAGACAGGATCTCACTTCGTTGCCCAGGCTGGAGTGCAGTG TTTAAGTCATAGGATTGATTAATTGAGACAGGGTCTCACTTCGTTGCCCAGGCTGGAGTGCAGTG T C SMAD2 Ensembl:ENSG00000175387 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs546951990 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_189980,RMVar_hsa_circ_189979,RMVar_hsa_circ_85065,RMVar_hsa_circ_267989,RMVar_hsa_circ_28288,RMVar_hsa_circ_8623,RMVar_hsa_circ_189985,RMVar_hsa_circ_189982,RMVar_hsa_circ_189983,RMVar_hsa_circ_318694,RMVar_hsa_circ_189984,RMVar_hsa_circ_328037,RMVar_hsa_circ_76285,RMVar_hsa_circ_119052,RMVar_hsa_circ_189987,RMVar_hsa_circ_189986,RMVar_hsa_circ_374009,RMVar_hsa_circ_189989,RMVar_hsa_circ_189991,RMVar_hsa_circ_189992,RMVar_hsa_circ_293362,RMVar_hsa_circ_289782,RMVar_hsa_circ_189993,RMVar_hsa_circ_189994,RMVar_hsa_circ_189995 34651 RMVar_ID_34651 Human_SNP_ID_646631159 A-to-I Human chr18 - 47860128 47860128 47860128 TCATTTAAGTCATAGGATTGATTAATTGAGACAGGATCTCACTTCGTTGCCCAGGCTGGAGTGCA TCATTTAAGTCATAGGATTGATTAATTGAGACGGGATCTCACTTCGTTGCCCAGGCTGGAGTGCA T C SMAD2 Ensembl:ENSG00000175387 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903215478 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_189980,RMVar_hsa_circ_189979,RMVar_hsa_circ_85065,RMVar_hsa_circ_267989,RMVar_hsa_circ_28288,RMVar_hsa_circ_8623,RMVar_hsa_circ_189985,RMVar_hsa_circ_189982,RMVar_hsa_circ_189983,RMVar_hsa_circ_318694,RMVar_hsa_circ_189984,RMVar_hsa_circ_328037,RMVar_hsa_circ_76285,RMVar_hsa_circ_119052,RMVar_hsa_circ_189987,RMVar_hsa_circ_189986,RMVar_hsa_circ_374009,RMVar_hsa_circ_189989,RMVar_hsa_circ_189991,RMVar_hsa_circ_189992,RMVar_hsa_circ_293362,RMVar_hsa_circ_289782,RMVar_hsa_circ_189993,RMVar_hsa_circ_189994,RMVar_hsa_circ_189995 34652 RMVar_ID_34652 Human_SNP_ID_646631237 A-to-I Human chr18 - 47860432 47860431 47860432 CAAAAAAAAATTTTTTTTTTTTTAAATTAGCCAGGGGTAGTGGCATTCACCTGTGGTCCCAGCTA CAAAAAAAAATTTTTTTTTTTTTAAATTAGCC_GGGGTAGTGGCATTCACCTGTGGTCCCAGCTA CT C SMAD2 Ensembl:ENSG00000175387 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277738814 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_2542956 RMVar_hsa_circ_189980,RMVar_hsa_circ_189979,RMVar_hsa_circ_85065,RMVar_hsa_circ_267989,RMVar_hsa_circ_28288,RMVar_hsa_circ_8623,RMVar_hsa_circ_189985,RMVar_hsa_circ_189982,RMVar_hsa_circ_189983,RMVar_hsa_circ_318694,RMVar_hsa_circ_189984,RMVar_hsa_circ_328037,RMVar_hsa_circ_76285,RMVar_hsa_circ_119052,RMVar_hsa_circ_189987,RMVar_hsa_circ_189986,RMVar_hsa_circ_374009,RMVar_hsa_circ_189989,RMVar_hsa_circ_189991,RMVar_hsa_circ_189992,RMVar_hsa_circ_293362,RMVar_hsa_circ_289782,RMVar_hsa_circ_189993,RMVar_hsa_circ_189994,RMVar_hsa_circ_189995 34653 RMVar_ID_34653 Human_SNP_ID_646645274 A-to-I Human chr18 - 47913016 47913016 47913016 ACTCCGGAGGCTGAGGCAGGAGAACTGCTTGAACCTGGGAGGTGGAGGTTGCAGTGAGCTGAGGT ACTCCGGAGGCTGAGGCAGGAGAACTGCTTGAGCCTGGGAGGTGGAGGTTGCAGTGAGCTGAGGT T C SMAD2 Ensembl:ENSG00000175387 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1230849242 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111810,RMVar_hsa_circ_63495,RMVar_hsa_circ_190005,RMVar_hsa_circ_60536 34654 RMVar_ID_34654 Human_SNP_ID_646844525 A-to-I Human chr18 + 48717830 48717825 48717830 TTCATTGCAGCCTTGAACTCCTGGCCTCAAGCAATCCTCCTGCCTCAGCCTCTTGAGTAGTTCTA TTCATTGCAGCCTTGAACTCCTGGCCTC_____ATCCTCCTGCCTCAGCCTCTTGAGTAGTTCTA CAAGCA C CTIF Ensembl:ENSG00000134030 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1235659390 Functional Loss DEL dbSNP153 29..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 34655 RMVar_ID_34655 Human_SNP_ID_646844536 A-to-I Human chr18 + 48717869 48717869 48717869 CTGCCTCAGCCTCTTGAGTAGTTCTAGGGACTATAGGCACCCGCCACCACACCTGACTAATTTTA CTGCCTCAGCCTCTTGAGTAGTTCTAGGGACTGTAGGCACCCGCCACCACACCTGACTAATTTTA A G CTIF Ensembl:ENSG00000134030 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1263325870 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 34656 RMVar_ID_34656 Human_SNP_ID_646844537 A-to-I Human chr18 + 48717871 48717871 48717871 GCCTCAGCCTCTTGAGTAGTTCTAGGGACTATAGGCACCCGCCACCACACCTGACTAATTTTATT GCCTCAGCCTCTTGAGTAGTTCTAGGGACTATGGGCACCCGCCACCACACCTGACTAATTTTATT A G CTIF Ensembl:ENSG00000134030 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444924958 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 34657 RMVar_ID_34657 Human_SNP_ID_646960139 A-to-I Human chr18 - 49159631 49159631 49159631 GTGATTGTCCTGCCTTGTCTTCCCAAGGTGCTAGGATTACAGGCATGAGCCACTGTGCCCTACAG GTGATTGTCCTGCCTTGTCTTCCCAAGGTGCTGGGATTACAGGCATGAGCCACTGTGCCCTACAG T C DYM Ensembl:ENSG00000141627 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1367220025 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50589,RMVar_hsa_circ_85747,RMVar_hsa_circ_107969,RMVar_hsa_circ_118103,RMVar_hsa_circ_99038,RMVar_hsa_circ_190031,RMVar_hsa_circ_190033,RMVar_hsa_circ_190034,RMVar_hsa_circ_190032,RMVar_hsa_circ_339710,RMVar_hsa_circ_362822,RMVar_hsa_circ_321151,RMVar_hsa_circ_58201,RMVar_hsa_circ_74321,RMVar_hsa_circ_342700,RMVar_hsa_circ_82855,RMVar_hsa_circ_190036,RMVar_hsa_circ_190037,RMVar_hsa_circ_371219,RMVar_hsa_circ_305630,RMVar_hsa_circ_341589,RMVar_hsa_circ_80110,RMVar_hsa_circ_190038,RMVar_hsa_circ_13465,RMVar_hsa_circ_50029,RMVar_hsa_circ_190039 34658 RMVar_ID_34658 Human_SNP_ID_646960140 A-to-I Human chr18 - 49159631 49159631 49159631 GTGATTGTCCTGCCTTGTCTTCCCAAGGTGCTAGGATTACAGGCATGAGCCACTGTGCCCTACAG GTGATTGTCCTGCCTTGTCTTCCCAAGGTGCTCGGATTACAGGCATGAGCCACTGTGCCCTACAG T G DYM Ensembl:ENSG00000141627 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1367220025 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50589,RMVar_hsa_circ_85747,RMVar_hsa_circ_107969,RMVar_hsa_circ_118103,RMVar_hsa_circ_99038,RMVar_hsa_circ_190031,RMVar_hsa_circ_190033,RMVar_hsa_circ_190034,RMVar_hsa_circ_190032,RMVar_hsa_circ_339710,RMVar_hsa_circ_362822,RMVar_hsa_circ_321151,RMVar_hsa_circ_58201,RMVar_hsa_circ_74321,RMVar_hsa_circ_342700,RMVar_hsa_circ_82855,RMVar_hsa_circ_190036,RMVar_hsa_circ_190037,RMVar_hsa_circ_371219,RMVar_hsa_circ_305630,RMVar_hsa_circ_341589,RMVar_hsa_circ_80110,RMVar_hsa_circ_190038,RMVar_hsa_circ_13465,RMVar_hsa_circ_50029,RMVar_hsa_circ_190039 34659 RMVar_ID_34659 Human_SNP_ID_646987004 A-to-I Human chr18 - 49263283 49263283 49263283 GAAACCCCATCTCTACTAAAAATACAAAAATTAGCCGAGTGTGCTGGTGGGTGCCTGTAATCCCA GAAACCCCATCTCTACTAAAAATACAAAAATTGGCCGAGTGTGCTGGTGGGTGCCTGTAATCCCA T C DYM Ensembl:ENSG00000141627 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs562540559 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26427,RMVar_hsa_circ_50589,RMVar_hsa_circ_85747,RMVar_hsa_circ_107969,RMVar_hsa_circ_118103,RMVar_hsa_circ_99038,RMVar_hsa_circ_190031,RMVar_hsa_circ_190033,RMVar_hsa_circ_190034,RMVar_hsa_circ_190032,RMVar_hsa_circ_321151,RMVar_hsa_circ_74321,RMVar_hsa_circ_342700,RMVar_hsa_circ_82855,RMVar_hsa_circ_190037,RMVar_hsa_circ_371219,RMVar_hsa_circ_305630,RMVar_hsa_circ_80110,RMVar_hsa_circ_190038,RMVar_hsa_circ_13465,RMVar_hsa_circ_50029,RMVar_hsa_circ_190039,RMVar_hsa_circ_322008,RMVar_hsa_circ_360296,RMVar_hsa_circ_323701,RMVar_hsa_circ_301984,RMVar_hsa_circ_78152,RMVar_hsa_circ_125129,RMVar_hsa_circ_21236,RMVar_hsa_circ_190040,RMVar_hsa_circ_190042,RMVar_hsa_circ_3529,RMVar_hsa_circ_190041,RMVar_hsa_circ_190045,RMVar_hsa_circ_26917,RMVar_hsa_circ_300703,RMVar_hsa_circ_303179,RMVar_hsa_circ_314925,RMVar_hsa_circ_190046,RMVar_hsa_circ_281282,RMVar_hsa_circ_314851,RMVar_hsa_circ_333073,RMVar_hsa_circ_348604,RMVar_hsa_circ_329650,RMVar_hsa_circ_281599,RMVar_hsa_circ_277020,RMVar_hsa_circ_36138,RMVar_hsa_circ_190047,RMVar_hsa_circ_190049,RMVar_hsa_circ_190051,RMVar_hsa_circ_190053,RMVar_hsa_circ_190052,RMVar_hsa_circ_190050,RMVar_hsa_circ_190048,RMVar_hsa_circ_67644 34660 RMVar_ID_34660 Human_SNP_ID_647001680 A-to-I Human chr18 - 49318375 49318374 49318375 GACCTCTCGAGCTGCCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCATGCC GACCTCTCGAGCTGCCTGCCTTGGCCTCCCAA_GTGCTGGGATTACAGGCGTGAGCCACCATGCC CT C DYM Ensembl:ENSG00000141627 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs74174750 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_26427,RMVar_hsa_circ_85747,RMVar_hsa_circ_107969,RMVar_hsa_circ_118103,RMVar_hsa_circ_99038,RMVar_hsa_circ_190031,RMVar_hsa_circ_190033,RMVar_hsa_circ_190034,RMVar_hsa_circ_190032,RMVar_hsa_circ_321151,RMVar_hsa_circ_74321,RMVar_hsa_circ_342700,RMVar_hsa_circ_13465,RMVar_hsa_circ_322008,RMVar_hsa_circ_360296,RMVar_hsa_circ_78152,RMVar_hsa_circ_125129,RMVar_hsa_circ_21236,RMVar_hsa_circ_190040,RMVar_hsa_circ_190041,RMVar_hsa_circ_26917,RMVar_hsa_circ_314925,RMVar_hsa_circ_333073,RMVar_hsa_circ_348604,RMVar_hsa_circ_281599,RMVar_hsa_circ_36138,RMVar_hsa_circ_190047,RMVar_hsa_circ_190049,RMVar_hsa_circ_190048,RMVar_hsa_circ_298617,RMVar_hsa_circ_330843,RMVar_hsa_circ_317473,RMVar_hsa_circ_190058,RMVar_hsa_circ_190059,RMVar_hsa_circ_329993,RMVar_hsa_circ_349612,RMVar_hsa_circ_364350,RMVar_hsa_circ_283054,RMVar_hsa_circ_66383,RMVar_hsa_circ_190064,RMVar_hsa_circ_122073,RMVar_hsa_circ_289959,RMVar_hsa_circ_190060,RMVar_hsa_circ_287088,RMVar_hsa_circ_190066,RMVar_hsa_circ_80467,RMVar_hsa_circ_190067,RMVar_hsa_circ_190065,RMVar_hsa_circ_190063 34661 RMVar_ID_34661 Human_SNP_ID_647018913 A-to-I Human chr18 - 49389635 49389635 49389635 AAACTTAACCAGGCATGGTGGCATGTGCCTGTAGTCTCAGCTGCTTGCGAGATTGAGGTAGGAGG AAACTTAACCAGGCATGGTGGCATGTGCCTGTGGTCTCAGCTGCTTGCGAGATTGAGGTAGGAGG T C DYM Ensembl:ENSG00000141627 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs568556217 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13465,RMVar_hsa_circ_360296,RMVar_hsa_circ_78152,RMVar_hsa_circ_21236,RMVar_hsa_circ_190040,RMVar_hsa_circ_333073,RMVar_hsa_circ_36138,RMVar_hsa_circ_77787,RMVar_hsa_circ_190047,RMVar_hsa_circ_330843,RMVar_hsa_circ_329993,RMVar_hsa_circ_80467,RMVar_hsa_circ_190067,RMVar_hsa_circ_305583,RMVar_hsa_circ_47094,RMVar_hsa_circ_333562,RMVar_hsa_circ_190068,RMVar_hsa_circ_190070,RMVar_hsa_circ_190069,RMVar_hsa_circ_287549,RMVar_hsa_circ_330646,RMVar_hsa_circ_303942,RMVar_hsa_circ_190077,RMVar_hsa_circ_190078,RMVar_hsa_circ_315754,RMVar_hsa_circ_359273 34662 RMVar_ID_34662 Human_SNP_ID_647025214 A-to-I Human chr18 - 49415099 49415099 49415099 TGGCTGGTCTCAAACTCCTGACTTCAGGTTGAAGCAGGAGAATCGCTTGAGCCCTGGAAACAGAG TGGCTGGTCTCAAACTCCTGACTTCAGGTTGAGGCAGGAGAATCGCTTGAGCCCTGGAAACAGAG T C DYM Ensembl:ENSG00000141627 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749195694 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13465,RMVar_hsa_circ_78152,RMVar_hsa_circ_190040,RMVar_hsa_circ_36138,RMVar_hsa_circ_77787,RMVar_hsa_circ_80467,RMVar_hsa_circ_190067,RMVar_hsa_circ_333562,RMVar_hsa_circ_190068,RMVar_hsa_circ_190069,RMVar_hsa_circ_287549,RMVar_hsa_circ_190078,RMVar_hsa_circ_315754,RMVar_hsa_circ_190079,RMVar_hsa_circ_302026 34663 RMVar_ID_34663 Human_SNP_ID_647042283 A-to-I Human chr18 - 49478408 49478407 49478408 AATACAAAAATTAGTCGGGCATAGTGGTACACACCTGTAATCCCAGCTACTCCAGAGGCTGAGGC AATACAAAAATTAGTCGGGCATAGTGGTACAC_CCTGTAATCCCAGCTACTCCAGAGGCTGAGGC GT G C18orf32 Ensembl:ENSG00000177576 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879359840 Functional Loss DEL dbSNP153 33..33 33 - - - 34664 RMVar_ID_34664 Human_SNP_ID_647044228 A-to-I Human chr18 - 49484920 49484920 49484920 GCTCCACCATGGCTGGCTAATTTTGTGTTTTTAGTAGAGACGGGGTTTCACCATGTTGGTTAGGC GCTCCACCATGGCTGGCTAATTTTGTGTTTTTGGTAGAGACGGGGTTTCACCATGTTGGTTAGGC T C C18orf32,AC100778.2,RPL17-C18orf32 Ensembl:ENSG00000177576,Ensembl:ENSG00000263916,Ensembl:ENSG00000215472 Protein coding,lincRNA,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs929270106 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13319559 34665 RMVar_ID_34665 Human_SNP_ID_647132115 A-to-I Human chr18 + 49820464 49820464 49820464 CCAGCATCAGAGAAAGGCAGTCTCCCGATAGAAAACACATGAAACTGGTGATCAGCCACTTCCTG CCAGCATCAGAGAAAGGCAGTCTCCCGATAGAGAACACATGAAACTGGTGATCAGCCACTTCCTG A G SNHG22 Ensembl:ENSG00000267322 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1449768175 Functional Loss SNV dbSNP153 33..33 33 - - - 34666 RMVar_ID_34666 Human_SNP_ID_647230497 A-to-I Human chr18 - 50187716 50187716 50187716 ACCCAGGAGTTCGAGACTAGCCTGGACAACATAGCGAGACCTCATCTCTACAAAAAATAGAAAAA ACCCAGGAGTTCGAGACTAGCCTGGACAACATGGCGAGACCTCATCTCTACAAAAAATAGAAAAA T C MYO5B Ensembl:ENSG00000167306 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1278456793 Functional Loss SNV dbSNP153 33..33 33 - - - 34667 RMVar_ID_34667 Human_SNP_ID_647248710 A-to-I Human chr18 - 50260479 50260479 50260479 TTTGTATTTTTTGTAGAGATGGGGGTTTCGTCATGTTGCGCAGGGTGGTTTTGAACTCTTGGACT TTTGTATTTTTTGTAGAGATGGGGGTTTCGTCGTGTTGCGCAGGGTGGTTTTGAACTCTTGGACT T C CFAP53 Ensembl:ENSG00000172361 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1408784380 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7391,RMVar_hsa_circ_69187 34668 RMVar_ID_34668 Human_SNP_ID_647255197 A-to-I Human chr18 - 50282708 50282708 50282708 GTGGTACAAGCTGGACGAGCTGTTTGAGCAGGAGCGCAATGTGCGCACAGCCATGACAAACCGCG GTGGTACAAGCTGGACGAGCTGTTTGAGCAGGTGCGCAATGTGCGCACAGCCATGACAAACCGCG T A CXXC1 Ensembl:ENSG00000154832 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1281002360 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_279034,Human_RBP_ID_509185,Human_RBP_ID_5583194,Human_RBP_ID_8472391,Human_RBP_ID_18717909,Human_RBP_ID_22064244 Human_Splice_Rec_1912754,Human_Splice_Rec_1912782,Human_Splice_Rec_1912810,Human_Splice_Rec_1912834,Human_Splice_Rec_1912860,Human_Splice_Rec_1912886,Human_Splice_Rec_1912888,Human_Splice_Rec_1912892 RMVar_hsa_circ_190126,RMVar_hsa_circ_114169 34669 RMVar_ID_34669 Human_SNP_ID_647256183 A-to-I Human chr18 - 50285353 50285353 50285353 GGGGCTGACCTGGGCCTTCCTCCTGCCGGCACAGGAATCGTACAAGTACTTCCCTTCCTCGGTGA GGGGCTGACCTGGGCCTTCCTCCTGCCGGCACGGGAATCGTACAAGTACTTCCCTTCCTCGGTGA T C CXXC1 Ensembl:ENSG00000154832 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs112730220 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_823173,Human_RBP_ID_5319612,Human_RBP_ID_19087254,Human_RBP_ID_21976969 Human_Splice_Rec_1912737,Human_Splice_Rec_1912765,Human_Splice_Rec_1912793,Human_Splice_Rec_1912817,Human_Splice_Rec_1912919,Human_Splice_Rec_1912939 RMVar_hsa_circ_95488,RMVar_hsa_circ_100072,RMVar_hsa_circ_190127,RMVar_hsa_circ_119529,RMVar_hsa_circ_190129,RMVar_hsa_circ_190130 34670 RMVar_ID_34670 Human_SNP_ID_647282647 A-to-I Human chr18 + 50392809 50392809 50392809 CGGACTGCAGCGGCGCTATCTCGGCTCACTGCAAACTCTGCCTCCCAGGTTCACGCCATCCTCCT CGGACTGCAGCGGCGCTATCTCGGCTCACTGCGAACTCTGCCTCCCAGGTTCACGCCATCCTCCT A G SKA1 Ensembl:ENSG00000154839 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348666530 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26462549,Human_RBP_ID_27461554 RMVar_hsa_circ_84889,RMVar_hsa_circ_118795,RMVar_hsa_circ_190132,RMVar_hsa_circ_82060,RMVar_hsa_circ_190133,RMVar_hsa_circ_190134 34671 RMVar_ID_34671 Human_SNP_ID_647282759 A-to-I Human chr18 + 50393235 50393235 50393235 GTCCCAGCTACTCAGGAGAATTGCTTGAACCTAGGAGGTGGAGGTTGCAGTGAGCCGAGATCGTG GTCCCAGCTACTCAGGAGAATTGCTTGAACCTGGGAGGTGGAGGTTGCAGTGAGCCGAGATCGTG A G SKA1 Ensembl:ENSG00000154839 Protein coding 3'UTR GSE100210;GSE99789;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,29796672,31158229,31158229 RNA-Seq:(High) rs566464998 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84889,RMVar_hsa_circ_118795,RMVar_hsa_circ_190132,RMVar_hsa_circ_82060,RMVar_hsa_circ_190133,RMVar_hsa_circ_190134 34672 RMVar_ID_34672 Human_SNP_ID_647351345 A-to-I Human chr18 + 50683188 50683188 50683188 GTTGCCCAGGCTGGAGTGCAGTGGCGTGATCTAAGCTCACTGCAATCTCCATCCCCCAGGTTCAA GTTGCCCAGGCTGGAGTGCAGTGGCGTGATCTGAGCTCACTGCAATCTCCATCCCCCAGGTTCAA A G MAPK4 Ensembl:ENSG00000141639 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1019723533 Functional Loss SNV dbSNP153 33..33 33 - - - 34673 RMVar_ID_34673 Human_SNP_ID_647352761 A-to-I Human chr18 + 50689277 50689277 50689277 AAATTATCCCAGGTGTGGTGGTGCAAGCCTGTAATCCCAGCTACTCGAGAGGCTGAGGCAGGAAA AAATTATCCCAGGTGTGGTGGTGCAAGCCTGTGATCCCAGCTACTCGAGAGGCTGAGGCAGGAAA A G MAPK4 Ensembl:ENSG00000141639 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1267639762 Functional Loss SNV dbSNP153 33..33 33 - - - 34674 RMVar_ID_34674 Human_SNP_ID_647360825 A-to-I Human chr18 + 50725107 50725107 50725107 ATTCATGCTGGTTAGCAAACAGCCTCTCGCACAAGGCTTCTGAGTGTCCCTTCCCTTCCCCAGGT ATTCATGCTGGTTAGCAAACAGCCTCTCGCACCAGGCTTCTGAGTGTCCCTTCCCTTCCCCAGGT A C MAPK4 Ensembl:ENSG00000141639 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs142754856 Functional Loss SNV dbSNP153 33..33 33 - - - 34675 RMVar_ID_34675 Human_SNP_ID_647380398 A-to-I Human chr18 - 50802832 50802832 50802832 CCCTAAGCCAGGCATGGTGGTGTGTGCCTGTAATCCCAGCTACTTAGGAGGCTGAGGCATGAGGG CCCTAAGCCAGGCATGGTGGTGTGTGCCTGTAGTCCCAGCTACTTAGGAGGCTGAGGCATGAGGG T C MRO Ensembl:ENSG00000134042 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1429052410 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55777 34676 RMVar_ID_34676 Human_SNP_ID_647400976 A-to-I Human chr18 + 50882828 50882828 50882828 AAAATTTGCTGGGCATGGTAGCACACACCTATAATCCCAGCTACTCAGTAGGCTGAGGCAGGAGA AAAATTTGCTGGGCATGGTAGCACACACCTATGATCCCAGCTACTCAGTAGGCTGAGGCAGGAGA A G ME2 Ensembl:ENSG00000082212 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1365802938 Functional Loss SNV dbSNP153 33..33 33 - - - 34677 RMVar_ID_34677 Human_SNP_ID_647401001 A-to-I Human chr18 + 50882949 50882949 50882949 CCAGCCTGGGCGACAGTGATTTTTGAGACTCTATCTCAAAAAAACAAACAAAAAAACTACTGCAA CCAGCCTGGGCGACAGTGATTTTTGAGACTCTGTCTCAAAAAAACAAACAAAAAAACTACTGCAA A G ME2 Ensembl:ENSG00000082212 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1345803590 Functional Loss SNV dbSNP153 33..33 33 - - - 34678 RMVar_ID_34678 Human_SNP_ID_647401601 A-to-I Human chr18 + 50885319 50885319 50885319 GAGATCGGACGATTGCTTGAGGCCAAGAGTTCAAGACCAGCCTGGGCAACATAGCAAACGCCAGC GAGATCGGACGATTGCTTGAGGCCAAGAGTTCGAGACCAGCCTGGGCAACATAGCAAACGCCAGC A G ME2 Ensembl:ENSG00000082212 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1292874148 Functional Loss SNV dbSNP153 33..33 33 - - - 34679 RMVar_ID_34679 Human_SNP_ID_647401948 A-to-I Human chr18 + 50886739 50886739 50886739 AAAACCAAATCTGGCTGGATGCAGTGGCTCACACCTGTAATCTCAGCACTTTGGGAGGCCAAGAC AAAACCAAATCTGGCTGGATGCAGTGGCTCACGCCTGTAATCTCAGCACTTTGGGAGGCCAAGAC A G ME2 Ensembl:ENSG00000082212 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1391295915 Functional Loss SNV dbSNP153 33..33 33 - - - 34680 RMVar_ID_34680 Human_SNP_ID_647412969 A-to-I Human chr18 + 50932759 50932759 50932759 GTGACTGATAGATTTATTTCCCAGGTTCAAGCAGTTCCCCTGCCTCAGCCTCCCGAGTATCTGGG GTGACTGATAGATTTATTTCCCAGGTTCAAGCGGTTCCCCTGCCTCAGCCTCCCGAGTATCTGGG A G ME2 Ensembl:ENSG00000082212 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1294762749 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_290097,RMVar_hsa_circ_190143,RMVar_hsa_circ_281838,RMVar_hsa_circ_39214,RMVar_hsa_circ_68413,RMVar_hsa_circ_87206,RMVar_hsa_circ_273482,RMVar_hsa_circ_190153,RMVar_hsa_circ_190154,RMVar_hsa_circ_120754,RMVar_hsa_circ_285710,RMVar_hsa_circ_190157,RMVar_hsa_circ_190156,RMVar_hsa_circ_190160,RMVar_hsa_circ_294793 34681 RMVar_ID_34681 Human_SNP_ID_647416450 A-to-I Human chr18 + 50947397 50947397 50947397 GCCCACCAGCACCCTACAGTCAGATAGTTGTGATGCTTTAATTCTAACATACAGCCCGTACCACA GCCCACCAGCACCCTACAGTCAGATAGTTGTGGTGCTTTAATTCTAACATACAGCCCGTACCACA A G ME2 Ensembl:ENSG00000082212 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs527710919 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17265401,Human_RBP_ID_23772613 Human_miRNA_ID_1523581 RMVar_hsa_circ_87206,RMVar_hsa_circ_190154,RMVar_hsa_circ_120754,RMVar_hsa_circ_190156 34682 RMVar_ID_34682 Human_SNP_ID_647446133 A-to-I Human chr18 + 51068896 51068896 51068896 AGAGCCATGATCATGCCACTGTGCTCCAGACTAGGTGATAGAGTGAGACCCTTTCTCAAAAATAA AGAGCCATGATCATGCCACTGTGCTCCAGACTGGGTGATAGAGTGAGACCCTTTCTCAAAAATAA A G SMAD4 Ensembl:ENSG00000141646 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1458091111 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51291,RMVar_hsa_circ_67256,RMVar_hsa_circ_370863,RMVar_hsa_circ_190176 34683 RMVar_ID_34683 Human_SNP_ID_647473960 A-to-I Human chr18 - 51176482 51176482 51176482 ACGACTGTGTGATTTGCTTTGAGAATGAGGTTATTGCTGCCCTAGTTCCATGTGGCCACAACCTC ACGACTGTGTGATTTGCTTTGAGAATGAGGTTTTTGCTGCCCTAGTTCCATGTGGCCACAACCTC T A MEX3C Ensembl:ENSG00000176624 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1470893321 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_509332,Human_RBP_ID_1550581,Human_RBP_ID_8472501,Human_RBP_ID_23772778 RMVar_hsa_circ_190180 34684 RMVar_ID_34684 Human_SNP_ID_647474562 A-to-I Human chr18 - 51178694 51178694 51178694 CACCACGCCCAGCTAATTTTTGTGTATTTAGTAAAGACGGGGTTTCACCATGTTCACCATGTTAG CACCACGCCCAGCTAATTTTTGTGTATTTAGTGAAGACGGGGTTTCACCATGTTCACCATGTTAG T C MEX3C Ensembl:ENSG00000176624 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1331851520 Functional Loss SNV dbSNP153 33..33 33 - - - 34685 RMVar_ID_34685 Human_SNP_ID_647474594 A-to-I Human chr18 - 51178797 51178797 51178797 GGAGTGCAGTGGGACAATCTCGGCTCACTGCAACCTCTGTCCCCCGGGTTCGAGCAATTCTTCTG GGAGTGCAGTGGGACAATCTCGGCTCACTGCAGCCTCTGTCCCCCGGGTTCGAGCAATTCTTCTG T C MEX3C Ensembl:ENSG00000176624 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1228103956 Functional Loss SNV dbSNP153 33..33 33 - - - 34686 RMVar_ID_34686 Human_SNP_ID_648096225 A-to-I Human chr18 + 53535025 53535025 53535025 AATAAACACAGGGGCATGGGCCAAGGGATCTCACTGTGTGCTGAACATGTATTTTCAGATGCAAG AATAAACACAGGGGCATGGGCCAAGGGATCTCGCTGTGTGCTGAACATGTATTTTCAGATGCAAG A G DCC Ensembl:ENSG00000187323 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs780297972 Functional Loss SNV dbSNP153 33..33 33 - - - 34687 RMVar_ID_34687 Human_SNP_ID_648096348 A-to-I Human chr18 + 53535620 53535620 53535620 TTGTTACAAAACACCTTTTTTAACAAAAAGGTATTTTGAGCCTACAAAAAGTTTCTTTAAACTGT TTGTTACAAAACACCTTTTTTAACAAAAAGGTGTTTTGAGCCTACAAAAAGTTTCTTTAAACTGT A G DCC Ensembl:ENSG00000187323 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1041625232 Functional Loss SNV dbSNP153 33..33 33 - - - 34688 RMVar_ID_34688 Human_SNP_ID_648271924 A-to-I Human chr18 - 54214374 54214372 54214374 GCTAACATAGTGAGACTCCTGTCCCTACAAAAAATTTTTAAAAATTAGCTGGGCATGTTGGCCTG GCTAACATAGTGAGACTCCTGTCCCTACAAAA__TTTTTAAAAATTAGCTGGGCATGTTGGCCTG ATT A MBD2 Ensembl:ENSG00000134046 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1568094245 Functional Loss DEL dbSNP153 33..34 33 - - - 34689 RMVar_ID_34689 Human_SNP_ID_648271927 A-to-I Human chr18 - 54214375 54214375 54214375 GGCTAACATAGTGAGACTCCTGTCCCTACAAAAAATTTTTAAAAATTAGCTGGGCATGTTGGCCT GGCTAACATAGTGAGACTCCTGTCCCTACAAAGAATTTTTAAAAATTAGCTGGGCATGTTGGCCT T C MBD2 Ensembl:ENSG00000134046 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1568094246 Functional Loss SNV dbSNP153 33..33 33 - - - 34690 RMVar_ID_34690 Human_SNP_ID_648271928 A-to-I Human chr18 - 54214377 54214377 54214377 CTGGCTAACATAGTGAGACTCCTGTCCCTACAAAAAATTTTTAAAAATTAGCTGGGCATGTTGGC CTGGCTAACATAGTGAGACTCCTGTCCCTACACAAAATTTTTAAAAATTAGCTGGGCATGTTGGC T G MBD2 Ensembl:ENSG00000134046 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs957434917 Functional Loss SNV dbSNP153 33..33 33 - - - 34691 RMVar_ID_34691 Human_SNP_ID_648271930 A-to-I Human chr18 - 54214380 54214380 54214380 AGCCTGGCTAACATAGTGAGACTCCTGTCCCTACAAAAAATTTTTAAAAATTAGCTGGGCATGTT AGCCTGGCTAACATAGTGAGACTCCTGTCCCTGCAAAAAATTTTTAAAAATTAGCTGGGCATGTT T C MBD2 Ensembl:ENSG00000134046 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1423359786 Functional Loss SNV dbSNP153 33..33 33 - - - 34692 RMVar_ID_34692 Human_SNP_ID_648272287 A-to-I Human chr18 - 54215628 54215628 54215628 AGATGGGCGTGGTGATGTGTGTCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCT AGATGGGCGTGGTGATGTGTGTCTGTAATCCCTGCTACTCGGGAGGCTGAGGCAGGAGAATTGCT T A MBD2 Ensembl:ENSG00000134046 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs752874801 Functional Loss SNV dbSNP153 33..33 33 - - - 34693 RMVar_ID_34693 Human_SNP_ID_648272289 A-to-I Human chr18 - 54215633 54215633 54215633 AAATTAGATGGGCGTGGTGATGTGTGTCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAA AAATTAGATGGGCGTGGTGATGTGTGTCTGTACTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAA T G MBD2 Ensembl:ENSG00000134046 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1390421566 Functional Loss SNV dbSNP153 33..33 33 - - - 34694 RMVar_ID_34694 Human_SNP_ID_648272607 A-to-I Human chr18 - 54216886 54216886 54216886 AGATTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGAACTCAGGTGATCCACCTGCTTTGGC AGATTTCACCATGTTGGCCAGGCTGGTCTCGACCTCCTGAACTCAGGTGATCCACCTGCTTTGGC T G MBD2 Ensembl:ENSG00000134046 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1298710915 Functional Loss SNV dbSNP153 33..33 33 - - - 34695 RMVar_ID_34695 Human_SNP_ID_648273010 A-to-I Human chr18 - 54218564 54218564 54218564 TGCTTGGGGTTGTACAGCTAGTAAGTGCAAAGATACAACCTGAAGCTGGTGGTTTAACCTCAGAA TGCTTGGGGTTGTACAGCTAGTAAGTGCAAAGGTACAACCTGAAGCTGGTGGTTTAACCTCAGAA T C MBD2 Ensembl:ENSG00000134046 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs570867 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_3864,GWAS_ID_3865,GWAS_ID_3866 34696 RMVar_ID_34696 Human_SNP_ID_648273107 A-to-I Human chr18 - 54218915 54218915 54218915 CTTTGTCACCTAGGCTGGAGTGCAGTGGTGCAATCTCAGCTCACTGCAACCTCCGCCTCCTGGGT CTTTGTCACCTAGGCTGGAGTGCAGTGGTGCAGTCTCAGCTCACTGCAACCTCCGCCTCCTGGGT T C MBD2 Ensembl:ENSG00000134046 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048302546 Functional Loss SNV dbSNP153 33..33 33 - - - 34697 RMVar_ID_34697 Human_SNP_ID_648273718 A-to-I Human chr18 - 54221268 54221268 54221268 ATCTTTTAGTAGAGACAGGGTTTTACCGTGTTAGCCAGGATGGTCTCGATCTCCTGACCTCGTGA ATCTTTTAGTAGAGACAGGGTTTTACCGTGTTGGCCAGGATGGTCTCGATCTCCTGACCTCGTGA T C MBD2 Ensembl:ENSG00000134046 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1281467621 Functional Loss SNV dbSNP153 33..33 33 - - - 34698 RMVar_ID_34698 Human_SNP_ID_648595954 A-to-I Human chr18 - 55546084 55546084 55546084 TCATTCTCCTGCCTCGGCCTCCCAAAGTGCTGAGATTTACAGGCATGAGCCACTGGACCCTGCAC TCATTCTCCTGCCTCGGCCTCCCAAAGTGCTGTGATTTACAGGCATGAGCCACTGGACCCTGCAC T A TCF4 Ensembl:ENSG00000196628 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs914772208 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_52518,RMVar_hsa_circ_305713,RMVar_hsa_circ_39929 34699 RMVar_ID_34699 Human_SNP_ID_648844616 A-to-I Human chr18 - 56611818 56611818 56611818 AAAAATTAGCCGGGTGTGCTGGTGGGCTACTCAGGAGGCTGAGGCTGGAGAATCGTTTGAACCTG AAAAATTAGCCGGGTGTGCTGGTGGGCTACTCGGGAGGCTGAGGCTGGAGAATCGTTTGAACCTG T C TXNL1 Ensembl:ENSG00000091164 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs926966152 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58384,RMVar_hsa_circ_107194,RMVar_hsa_circ_117355,RMVar_hsa_circ_190273,RMVar_hsa_circ_190274,RMVar_hsa_circ_277502,RMVar_hsa_circ_328975,RMVar_hsa_circ_22222,RMVar_hsa_circ_43217,RMVar_hsa_circ_190275 34700 RMVar_ID_34700 Human_SNP_ID_648844677 A-to-I Human chr18 - 56611987 56611987 56611987 AAGATTAGCCGGGCGTGGCAGCATGTGCCTGTAGTCCCCCCTCCTCAGGAGGCTGAGGCAGGAGA AAGATTAGCCGGGCGTGGCAGCATGTGCCTGTGGTCCCCCCTCCTCAGGAGGCTGAGGCAGGAGA T C TXNL1 Ensembl:ENSG00000091164 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs939745768 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58384,RMVar_hsa_circ_107194,RMVar_hsa_circ_117355,RMVar_hsa_circ_190273,RMVar_hsa_circ_190274,RMVar_hsa_circ_277502,RMVar_hsa_circ_328975,RMVar_hsa_circ_22222,RMVar_hsa_circ_43217,RMVar_hsa_circ_190275 34701 RMVar_ID_34701 Human_SNP_ID_648844985 A-to-I Human chr18 - 56613091 56613091 56613091 TCACTCCTGTAATCCCAGCATTTTGGGAGGCCAAGATGGGCAGATTGCTCGAGCCCATGATTTTG TCACTCCTGTAATCCCAGCATTTTGGGAGGCCGAGATGGGCAGATTGCTCGAGCCCATGATTTTG T C TXNL1 Ensembl:ENSG00000091164 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs937315069 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25368063 RMVar_hsa_circ_58384,RMVar_hsa_circ_107194,RMVar_hsa_circ_117355,RMVar_hsa_circ_190273,RMVar_hsa_circ_190274,RMVar_hsa_circ_277502,RMVar_hsa_circ_328975,RMVar_hsa_circ_22222,RMVar_hsa_circ_43217,RMVar_hsa_circ_190275 34702 RMVar_ID_34702 Human_SNP_ID_648844986 A-to-I Human chr18 - 56613091 56613091 56613091 TCACTCCTGTAATCCCAGCATTTTGGGAGGCCAAGATGGGCAGATTGCTCGAGCCCATGATTTTG TCACTCCTGTAATCCCAGCATTTTGGGAGGCCCAGATGGGCAGATTGCTCGAGCCCATGATTTTG T G TXNL1 Ensembl:ENSG00000091164 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs937315069 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25368063 RMVar_hsa_circ_58384,RMVar_hsa_circ_107194,RMVar_hsa_circ_117355,RMVar_hsa_circ_190273,RMVar_hsa_circ_190274,RMVar_hsa_circ_277502,RMVar_hsa_circ_328975,RMVar_hsa_circ_22222,RMVar_hsa_circ_43217,RMVar_hsa_circ_190275 34703 RMVar_ID_34703 Human_SNP_ID_648845099 A-to-I Human chr18 - 56613754 56613754 56613754 CAGGCTGGAGTACAGTGGCACGACCTTGGTTCAGTATAGCCCTGATCTACTGGGCTCAGGTGATT CAGGCTGGAGTACAGTGGCACGACCTTGGTTCTGTATAGCCCTGATCTACTGGGCTCAGGTGATT T A TXNL1 Ensembl:ENSG00000091164 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs897666838 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5260991 RMVar_hsa_circ_58384,RMVar_hsa_circ_107194,RMVar_hsa_circ_117355,RMVar_hsa_circ_190273,RMVar_hsa_circ_190274,RMVar_hsa_circ_277502,RMVar_hsa_circ_328975,RMVar_hsa_circ_22222,RMVar_hsa_circ_43217,RMVar_hsa_circ_190275 34704 RMVar_ID_34704 Human_SNP_ID_648849251 A-to-I Human chr18 - 56629955 56629955 56629955 CCCTAAAGTGATCCACCTGCCTTGGCCTCCCAAAGTGCTGAGATTACAGGCATGAGCCATCATCG CCCTAAAGTGATCCACCTGCCTTGGCCTCCCAGAGTGCTGAGATTACAGGCATGAGCCATCATCG T C TXNL1 Ensembl:ENSG00000091164 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs536780939 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58384,RMVar_hsa_circ_361209 34705 RMVar_ID_34705 Human_SNP_ID_648882661 A-to-I Human chr18 + 56769433 56769433 56769433 ATTGCCCAGGCTGGTTTCGAACTCCTGGGCTCAAGTGATCCTCCCACCCCAACCTCCCAAAGTGC ATTGCCCAGGCTGGTTTCGAACTCCTGGGCTCCAGTGATCCTCCCACCCCAACCTCCCAAAGTGC A C WDR7 Ensembl:ENSG00000091157 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs932667388 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1594,RMVar_hsa_circ_29154,RMVar_hsa_circ_372319,RMVar_hsa_circ_190283,RMVar_hsa_circ_123749,RMVar_hsa_circ_190281,RMVar_hsa_circ_42855,RMVar_hsa_circ_364326,RMVar_hsa_circ_190287,RMVar_hsa_circ_292498,RMVar_hsa_circ_289365,RMVar_hsa_circ_53928,RMVar_hsa_circ_190297,RMVar_hsa_circ_67923,RMVar_hsa_circ_190289,RMVar_hsa_circ_190288,RMVar_hsa_circ_344253,RMVar_hsa_circ_281597,RMVar_hsa_circ_190294,RMVar_hsa_circ_190295,RMVar_hsa_circ_20866,RMVar_hsa_circ_288513,RMVar_hsa_circ_294396,RMVar_hsa_circ_190298,RMVar_hsa_circ_190300,RMVar_hsa_circ_296129,RMVar_hsa_circ_366403,RMVar_hsa_circ_281150,RMVar_hsa_circ_190299 34706 RMVar_ID_34706 Human_SNP_ID_649066992 A-to-I Human chr18 - 57547909 57547909 57547909 ATGTGAGGCTGGGTGCCGTGCCTTACATGTGTAATTCCAATACTTTGGAAGGCCAAGGTTGGAGG ATGTGAGGCTGGGTGCCGTGCCTTACATGTGTCATTCCAATACTTTGGAAGGCCAAGGTTGGAGG T G FECH Ensembl:ENSG00000066926 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971808666 Functional Loss SNV dbSNP153 33..33 33 - - - 34707 RMVar_ID_34707 Human_SNP_ID_649084723 A-to-I Human chr18 - 57618710 57618710 57618710 ATTTGTAGATACGAGATCTCATTATGTTTCCCAGGCTGGTCTTAAACTCCTGGGCTTAAGCAATC ATTTGTAGATACGAGATCTCATTATGTTTCCCCGGCTGGTCTTAAACTCCTGGGCTTAAGCAATC T G NARS1 Ensembl:ENSG00000134440 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1246557214 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13325343 RMVar_hsa_circ_110138,RMVar_hsa_circ_190320,RMVar_hsa_circ_89274,RMVar_hsa_circ_190329,RMVar_hsa_circ_190331,RMVar_hsa_circ_366430,RMVar_hsa_circ_88227,RMVar_hsa_circ_89382,RMVar_hsa_circ_190332,RMVar_hsa_circ_190335 34708 RMVar_ID_34708 Human_SNP_ID_649084751 A-to-I Human chr18 - 57618793 57618793 57618793 GGCTTAAGGGATCCTCCCACCTCAGCCTTCCAAGTAGCTCGGACCACAGGGGCATGTCACCACAC GGCTTAAGGGATCCTCCCACCTCAGCCTTCCAGGTAGCTCGGACCACAGGGGCATGTCACCACAC T C NARS1 Ensembl:ENSG00000134440 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1320853593 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13325346 RMVar_hsa_circ_110138,RMVar_hsa_circ_190320,RMVar_hsa_circ_89274,RMVar_hsa_circ_190329,RMVar_hsa_circ_190331,RMVar_hsa_circ_366430,RMVar_hsa_circ_88227,RMVar_hsa_circ_89382,RMVar_hsa_circ_190332,RMVar_hsa_circ_190335 34709 RMVar_ID_34709 Human_SNP_ID_649084766 A-to-I Human chr18 - 57618856 57618856 57618856 AATTTGTTGCCCAGGCTGGAGTGCAGTAGCGCATTCATGGCTCACTGCAGCTTCAACCTCCTGGG AATTTGTTGCCCAGGCTGGAGTGCAGTAGCGCGTTCATGGCTCACTGCAGCTTCAACCTCCTGGG T C NARS1 Ensembl:ENSG00000134440 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs888009053 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110138,RMVar_hsa_circ_190320,RMVar_hsa_circ_89274,RMVar_hsa_circ_190329,RMVar_hsa_circ_190331,RMVar_hsa_circ_366430,RMVar_hsa_circ_88227,RMVar_hsa_circ_89382,RMVar_hsa_circ_190332,RMVar_hsa_circ_190335 34710 RMVar_ID_34710 Human_SNP_ID_649084771 A-to-I Human chr18 - 57618861 57618861 57618861 ATCTTAATTTGTTGCCCAGGCTGGAGTGCAGTAGCGCATTCATGGCTCACTGCAGCTTCAACCTC ATCTTAATTTGTTGCCCAGGCTGGAGTGCAGTTGCGCATTCATGGCTCACTGCAGCTTCAACCTC T A NARS1 Ensembl:ENSG00000134440 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1252093226 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110138,RMVar_hsa_circ_190320,RMVar_hsa_circ_89274,RMVar_hsa_circ_190329,RMVar_hsa_circ_190331,RMVar_hsa_circ_366430,RMVar_hsa_circ_88227,RMVar_hsa_circ_89382,RMVar_hsa_circ_190332,RMVar_hsa_circ_190335 34711 RMVar_ID_34711 Human_SNP_ID_649084778 A-to-I Human chr18 - 57618909 57618905 57618909 GGGTACTTGTTTTTAATTTAACTTATTTATTTATTTTTCTGAGACAGGATCTTAATTTGTTGCCC GGGTACTTGTTTTTAATTTAACTTATTTATTT____TTCTGAGACAGGATCTTAATTTGTTGCCC AAAAT A NARS1 Ensembl:ENSG00000134440 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968571166 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_6697033 RMVar_hsa_circ_110138,RMVar_hsa_circ_190320,RMVar_hsa_circ_89274,RMVar_hsa_circ_190329,RMVar_hsa_circ_190331,RMVar_hsa_circ_366430,RMVar_hsa_circ_88227,RMVar_hsa_circ_89382,RMVar_hsa_circ_190332,RMVar_hsa_circ_190335 34712 RMVar_ID_34712 Human_SNP_ID_649084853 A-to-I Human chr18 - 57619197 57619197 57619197 CCAGCTACTCGGGAGACTGAGATAGGGGGATTACTTGAGCCCAGGAGGTTGAGGCTGCAGTGAGC CCAGCTACTCGGGAGACTGAGATAGGGGGATTGCTTGAGCCCAGGAGGTTGAGGCTGCAGTGAGC T C NARS1 Ensembl:ENSG00000134440 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1345582191 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110138,RMVar_hsa_circ_190320,RMVar_hsa_circ_89274,RMVar_hsa_circ_190329,RMVar_hsa_circ_190331,RMVar_hsa_circ_366430,RMVar_hsa_circ_88227,RMVar_hsa_circ_89382,RMVar_hsa_circ_190332,RMVar_hsa_circ_190335 34713 RMVar_ID_34713 Human_SNP_ID_649084855 A-to-I Human chr18 - 57619206 57619205 57619206 CCTGTGGCCCCAGCTACTCGGGAGACTGAGATAGGGGGATTACTTGAGCCCAGGAGGTTGAGGCT CCTGTGGCCCCAGCTACTCGGGAGACTGAGAT_GGGGGATTACTTGAGCCCAGGAGGTTGAGGCT CT C NARS1 Ensembl:ENSG00000134440 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs113965356 Functional Loss DEL dbSNP153 33..33 33 - - - GWAS_ID_3867,GWAS_ID_3868,GWAS_ID_3869,GWAS_ID_3870,GWAS_ID_3871,GWAS_ID_3872,GWAS_ID_3873,GWAS_ID_3874,GWAS_ID_3875,GWAS_ID_3876,GWAS_ID_3877,GWAS_ID_3878,GWAS_ID_3879,GWAS_ID_3880,GWAS_ID_3881 RMVar_hsa_circ_110138,RMVar_hsa_circ_190320,RMVar_hsa_circ_89274,RMVar_hsa_circ_190329,RMVar_hsa_circ_190331,RMVar_hsa_circ_366430,RMVar_hsa_circ_88227,RMVar_hsa_circ_89382,RMVar_hsa_circ_190332,RMVar_hsa_circ_190335 34714 RMVar_ID_34714 Human_SNP_ID_649085042 A-to-I Human chr18 - 57619963 57619963 57619963 TGGACTCAGGCCTGGTGTGGTGGCTCACGCCTATAATCTCAACACTTTGGGAGGCCGGGGCAGGT TGGACTCAGGCCTGGTGTGGTGGCTCACGCCTGTAATCTCAACACTTTGGGAGGCCGGGGCAGGT T C NARS1 Ensembl:ENSG00000134440 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs535104986 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110138,RMVar_hsa_circ_190320,RMVar_hsa_circ_89274,RMVar_hsa_circ_190329,RMVar_hsa_circ_190331,RMVar_hsa_circ_366430,RMVar_hsa_circ_88227,RMVar_hsa_circ_89382,RMVar_hsa_circ_190332,RMVar_hsa_circ_190335 34715 RMVar_ID_34715 Human_SNP_ID_649098105 A-to-I Human chr18 + 57667295 57667281 57667295 GCTGGAGTGCAGTGGCACAATCTCTGCTCACTACAGCCTCAACCTCCAGGATTCAAGTGATCTGC GCTGGAGTGCAGTGGCACGATCTCTGCTCACTGCAGCCTCAACCTCCAGGATTCAAGTGATCTGC AATCTCTGCTCACTA GATCTCTGCTCACTG AC027097.1,AC027097.2 Ensembl:ENSG00000267040,Ensembl:ENSG00000267787 lincRNA,lincRNA exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs386803630 Functional Loss MNV dbSNP153 19..33 33 - - - Human_Splice_Rec_1917916 RMVar_hsa_circ_83490,RMVar_hsa_circ_125710,RMVar_hsa_circ_190337,RMVar_hsa_circ_190338 34716 RMVar_ID_34716 Human_SNP_ID_649098107 A-to-I Human chr18 + 57667295 57667295 57667295 GCTGGAGTGCAGTGGCACAATCTCTGCTCACTACAGCCTCAACCTCCAGGATTCAAGTGATCTGC GCTGGAGTGCAGTGGCACAATCTCTGCTCACTGCAGCCTCAACCTCCAGGATTCAAGTGATCTGC A G AC027097.1,AC027097.2 Ensembl:ENSG00000267040,Ensembl:ENSG00000267787 lincRNA,lincRNA exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs317846 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1917916 Clinvar_Rec_107 RMVar_hsa_circ_83490,RMVar_hsa_circ_125710,RMVar_hsa_circ_190337,RMVar_hsa_circ_190338 34717 RMVar_ID_34717 Human_SNP_ID_649098108 A-to-I Human chr18 + 57667295 57667295 57667295 GCTGGAGTGCAGTGGCACAATCTCTGCTCACTACAGCCTCAACCTCCAGGATTCAAGTGATCTGC GCTGGAGTGCAGTGGCACAATCTCTGCTCACTTCAGCCTCAACCTCCAGGATTCAAGTGATCTGC A T AC027097.1,AC027097.2 Ensembl:ENSG00000267040,Ensembl:ENSG00000267787 lincRNA,lincRNA exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs317846 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1917916 Clinvar_Rec_107 RMVar_hsa_circ_83490,RMVar_hsa_circ_125710,RMVar_hsa_circ_190337,RMVar_hsa_circ_190338 34718 RMVar_ID_34718 Human_SNP_ID_649106263 A-to-I Human chr18 + 57699753 57699753 57699753 AAAAAAATAAAAAAAAAGACAGGAGTCTCACTAAGTTTTCCAGGCTGGCCTCGAACTCCTGGCCT AAAAAAATAAAAAAAAAGACAGGAGTCTCACTGAGTTTTCCAGGCTGGCCTCGAACTCCTGGCCT A G AC027097.2 Ensembl:ENSG00000267787 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1164546431 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125710,RMVar_hsa_circ_190338 34719 RMVar_ID_34719 Human_SNP_ID_649116121 A-to-I Human chr18 + 57738000 57738000 57738000 CGACTTCTCTGCAGTGTGCATGTGTGTGAAACACAGACACACACGGGAGGAATTTGGCTCTGTCA CGACTTCTCTGCAGTGTGCATGTGTGTGAAACGCAGACACACACGGGAGGAATTTGGCTCTGTCA A G AC027097.2 Ensembl:ENSG00000267787 lincRNA exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs404736 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_190359,RMVar_hsa_circ_107064 34720 RMVar_ID_34720 Human_SNP_ID_649116122 A-to-I Human chr18 + 57738000 57738000 57738000 CGACTTCTCTGCAGTGTGCATGTGTGTGAAACACAGACACACACGGGAGGAATTTGGCTCTGTCA CGACTTCTCTGCAGTGTGCATGTGTGTGAAACTCAGACACACACGGGAGGAATTTGGCTCTGTCA A T AC027097.2 Ensembl:ENSG00000267787 lincRNA exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs404736 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_190359,RMVar_hsa_circ_107064 34721 RMVar_ID_34721 Human_SNP_ID_649140452 A-to-I Human chr18 + 57838751 57838751 57838751 CAGCGAGAGCTATGGAATAAAACTATTGATGCAATGAAGAGAGTTGAAGAGATCAAACAGAAACA CAGCGAGAGCTATGGAATAAAACTATTGATGCGATGAAGAGAGTTGAAGAGATCAAACAGAAACA A G RSL24D1P11 Ensembl:ENSG00000231544 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1360392012 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26462705 34722 RMVar_ID_34722 Human_SNP_ID_649201267 A-to-I Human chr18 + 58082674 58082674 58082674 CATACATGTAGTCCCATCTACTTGAGCGTCTGAGGCAGGAGAATTGCTTGAACCTGGGAAGCGGA CATACATGTAGTCCCATCTACTTGAGCGTCTGCGGCAGGAGAATTGCTTGAACCTGGGAAGCGGA A C NEDD4L Ensembl:ENSG00000049759 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1015401117 Functional Loss SNV dbSNP153 33..33 33 - - - 34723 RMVar_ID_34723 Human_SNP_ID_649201896 A-to-I Human chr18 + 58084895 58084895 58084895 TTTCGTAATTTTGGTAGAGACTGGGTCTTCCTATGTTGCCCAGCCTGGTCTTGAATTCCTGGGCT TTTCGTAATTTTGGTAGAGACTGGGTCTTCCTGTGTTGCCCAGCCTGGTCTTGAATTCCTGGGCT A G NEDD4L Ensembl:ENSG00000049759 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1050146190 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23774644 34724 RMVar_ID_34724 Human_SNP_ID_649207550 A-to-I Human chr18 + 58107894 58107894 58107894 ATGCCACTATGCCCAGCTAATTTTTTTTTTGTATTTTTAGTAAAGATGGGGTTTTGCCATCTTGC ATGCCACTATGCCCAGCTAATTTTTTTTTTGTGTTTTTAGTAAAGATGGGGTTTTGCCATCTTGC A G NEDD4L Ensembl:ENSG00000049759 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027678044 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_190363 34725 RMVar_ID_34725 Human_SNP_ID_649207551 A-to-I Human chr18 + 58107894 58107894 58107894 ATGCCACTATGCCCAGCTAATTTTTTTTTTGTATTTTTAGTAAAGATGGGGTTTTGCCATCTTGC ATGCCACTATGCCCAGCTAATTTTTTTTTTGTTTTTTTAGTAAAGATGGGGTTTTGCCATCTTGC A T NEDD4L Ensembl:ENSG00000049759 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027678044 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_190363 34726 RMVar_ID_34726 Human_SNP_ID_649207553 A-to-I Human chr18 + 58107903 58107903 58107903 TGCCCAGCTAATTTTTTTTTTGTATTTTTAGTAAAGATGGGGTTTTGCCATCTTGCTTCTGCTGG TGCCCAGCTAATTTTTTTTTTGTATTTTTAGTGAAGATGGGGTTTTGCCATCTTGCTTCTGCTGG A G NEDD4L Ensembl:ENSG00000049759 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs964494107 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_190363 34727 RMVar_ID_34727 Human_SNP_ID_649238217 A-to-I Human chr18 + 58230986 58230967 58230987 AGGGACAAACAAGTCTGGACGTGGTGACTCATACCTGTAATTCCAACACTGTGGGAGGTGGAGGC AGGGACAAACAAGT____________________CTGTAATTCCAACACTGTGGGAGGTGGAGGC TCTGGACGTGGTGACTCATAC T NEDD4L Ensembl:ENSG00000049759 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1329375404 Functional Loss DEL dbSNP153 15..34 33 - - - RMVar_hsa_circ_6445,RMVar_hsa_circ_293960,RMVar_hsa_circ_335897,RMVar_hsa_circ_363960,RMVar_hsa_circ_302735,RMVar_hsa_circ_59427,RMVar_hsa_circ_272538,RMVar_hsa_circ_23556,RMVar_hsa_circ_86834,RMVar_hsa_circ_98265,RMVar_hsa_circ_190364,RMVar_hsa_circ_190365,RMVar_hsa_circ_190366,RMVar_hsa_circ_373635,RMVar_hsa_circ_190367,RMVar_hsa_circ_190368 34728 RMVar_ID_34728 Human_SNP_ID_649238228 A-to-I Human chr18 + 58230998 58230998 58230998 GTCTGGACGTGGTGACTCATACCTGTAATTCCAACACTGTGGGAGGTGGAGGCAGGAGGATCCCT GTCTGGACGTGGTGACTCATACCTGTAATTCCCACACTGTGGGAGGTGGAGGCAGGAGGATCCCT A C NEDD4L Ensembl:ENSG00000049759 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1456931062 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6445,RMVar_hsa_circ_293960,RMVar_hsa_circ_335897,RMVar_hsa_circ_363960,RMVar_hsa_circ_302735,RMVar_hsa_circ_59427,RMVar_hsa_circ_272538,RMVar_hsa_circ_23556,RMVar_hsa_circ_86834,RMVar_hsa_circ_98265,RMVar_hsa_circ_190364,RMVar_hsa_circ_190365,RMVar_hsa_circ_190366,RMVar_hsa_circ_373635,RMVar_hsa_circ_190367,RMVar_hsa_circ_190368 34729 RMVar_ID_34729 Human_SNP_ID_649254507 A-to-I Human chr18 + 58297625 58297625 58297625 TTGTAGGCTGAAAACTGGCCCACAGATTTATTAGGTCCTGACCCCTGGAACTTGTCAATGTTGCC TTGTAGGCTGAAAACTGGCCCACAGATTTATTGGGTCCTGACCCCTGGAACTTGTCAATGTTGCC A G NEDD4L Ensembl:ENSG00000049759 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1397126152 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17567364 RMVar_hsa_circ_6445,RMVar_hsa_circ_293960,RMVar_hsa_circ_335897,RMVar_hsa_circ_363960,RMVar_hsa_circ_302735,RMVar_hsa_circ_59427,RMVar_hsa_circ_60977,RMVar_hsa_circ_86834,RMVar_hsa_circ_190364,RMVar_hsa_circ_190368,RMVar_hsa_circ_342403,RMVar_hsa_circ_47925,RMVar_hsa_circ_55410,RMVar_hsa_circ_190370,RMVar_hsa_circ_190371,RMVar_hsa_circ_190372,RMVar_hsa_circ_76555 34730 RMVar_ID_34730 Human_SNP_ID_649302101 A-to-I Human chr18 - 58487787 58487787 58487787 GTATTCCTGGGCTCCAGCTAACCTCCTGTTTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG GTATTCCTGGGCTCCAGCTAACCTCCTGTTTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG T C ALPK2 Ensembl:ENSG00000198796 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1384825345 Functional Loss SNV dbSNP153 33..33 33 - - - 34731 RMVar_ID_34731 Human_SNP_ID_649302654 A-to-I Human chr18 - 58489965 58489965 58489965 GCGATTCTCCTGCCTCAGCCTCCTGAGTAGCTAAGACTACAGGCACACGGTACCACACCCAGCTA GCGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGAGACTACAGGCACACGGTACCACACCCAGCTA T C ALPK2 Ensembl:ENSG00000198796 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1482001533 Functional Loss SNV dbSNP153 33..33 33 - - - 34732 RMVar_ID_34732 Human_SNP_ID_649314949 A-to-I Human chr18 - 58538905 58538905 58538905 ATTTTCAGAGATAGTATGGACAGAGAGGAAGCAGGGTGGGGGTGGGGATGGTGCCAGACTCTTTT ATTTTCAGAGATAGTATGGACAGAGAGGAAGCGGGGTGGGGGTGGGGATGGTGCCAGACTCTTTT T C ALPK2 Ensembl:ENSG00000198796 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1279784638 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84169,RMVar_hsa_circ_190389,RMVar_hsa_circ_127569,RMVar_hsa_circ_190390 34733 RMVar_ID_34733 Human_SNP_ID_649315465 A-to-I Human chr18 - 58541309 58541309 58541309 TGAGTGAGTTCTTGTGAGATCTGGTTGTTTAAAAGTGTGCGGCACCTCCCCCTTGCTCGCTCTTG TGAGTGAGTTCTTGTGAGATCTGGTTGTTTAAGAGTGTGCGGCACCTCCCCCTTGCTCGCTCTTG T C ALPK2 Ensembl:ENSG00000198796 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1421648755 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84169,RMVar_hsa_circ_190389,RMVar_hsa_circ_127569,RMVar_hsa_circ_190390 34734 RMVar_ID_34734 Human_SNP_ID_649315493 A-to-I Human chr18 - 58541437 58541437 58541437 CTACCAAATCTTGCACTGAGATGTAATCCCCAATGTTGGAGGTGGGGCCCAGTGGGAGGTGATTG CTACCAAATCTTGCACTGAGATGTAATCCCCAGTGTTGGAGGTGGGGCCCAGTGGGAGGTGATTG T C ALPK2 Ensembl:ENSG00000198796 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs555303858 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84169,RMVar_hsa_circ_190389,RMVar_hsa_circ_127569,RMVar_hsa_circ_190390 34735 RMVar_ID_34735 Human_SNP_ID_649353815 A-to-I Human chr18 + 58702096 58702096 58702096 ATTTAAGAAACAGATTGTGGATCTGGCATGGTAGCTCACACCTGTAATCCCAGTACTTTGGGAAG ATTTAAGAAACAGATTGTGGATCTGGCATGGTGGCTCACACCTGTAATCCCAGTACTTTGGGAAG A G MALT1 Ensembl:ENSG00000172175 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1198984898 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2053,RMVar_hsa_circ_55577,RMVar_hsa_circ_357897,RMVar_hsa_circ_269120,RMVar_hsa_circ_74253,RMVar_hsa_circ_354556,RMVar_hsa_circ_324161,RMVar_hsa_circ_190395,RMVar_hsa_circ_190396 34736 RMVar_ID_34736 Human_SNP_ID_649357656 A-to-I Human chr18 + 58719020 58719020 58719020 GGTGTGGGTGAGGAACAAAGTTCAGTATTGCTAGAAGGTAGAAAACTAGGGAAGGAGTGGCTGGA GGTGTGGGTGAGGAACAAAGTTCAGTATTGCTGGAAGGTAGAAAACTAGGGAAGGAGTGGCTGGA A G MALT1 Ensembl:ENSG00000172175 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935315792 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2053,RMVar_hsa_circ_55577,RMVar_hsa_circ_357897,RMVar_hsa_circ_269120,RMVar_hsa_circ_65311,RMVar_hsa_circ_68166,RMVar_hsa_circ_318851,RMVar_hsa_circ_356856,RMVar_hsa_circ_288725,RMVar_hsa_circ_190398,RMVar_hsa_circ_190397,RMVar_hsa_circ_343682,RMVar_hsa_circ_46786,RMVar_hsa_circ_84771,RMVar_hsa_circ_378538,RMVar_hsa_circ_6674,RMVar_hsa_circ_316248,RMVar_hsa_circ_190400,RMVar_hsa_circ_190401 34737 RMVar_ID_34737 Human_SNP_ID_649362042 A-to-I Human chr18 + 58737355 58737355 58737355 ATTTAAAAAATTAGCCAGGCATTATGGTGTGCACCTGCAGTGCCAGCTACTCGCGAGACTTAGGT ATTTAAAAAATTAGCCAGGCATTATGGTGTGCGCCTGCAGTGCCAGCTACTCGCGAGACTTAGGT A G MALT1 Ensembl:ENSG00000172175 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1279970098 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25382,RMVar_hsa_circ_269120,RMVar_hsa_circ_356856,RMVar_hsa_circ_316248,RMVar_hsa_circ_190402,RMVar_hsa_circ_306785,RMVar_hsa_circ_126345,RMVar_hsa_circ_190405,RMVar_hsa_circ_190406,RMVar_hsa_circ_72251,RMVar_hsa_circ_323589 34738 RMVar_ID_34738 Human_SNP_ID_649362142 A-to-I Human chr18 + 58737631 58737631 58737631 TGTGAGACTACAGAGTCTCTGTCGCGCAGGCTAGAGTGCAGTGGCATGATCTTGGCTTACTGCAA TGTGAGACTACAGAGTCTCTGTCGCGCAGGCTGGAGTGCAGTGGCATGATCTTGGCTTACTGCAA A G MALT1 Ensembl:ENSG00000172175 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1262323860 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17567367 RMVar_hsa_circ_25382,RMVar_hsa_circ_269120,RMVar_hsa_circ_356856,RMVar_hsa_circ_316248,RMVar_hsa_circ_190402,RMVar_hsa_circ_306785,RMVar_hsa_circ_126345,RMVar_hsa_circ_190405,RMVar_hsa_circ_190406,RMVar_hsa_circ_72251,RMVar_hsa_circ_323589 34739 RMVar_ID_34739 Human_SNP_ID_649365939 A-to-I Human chr18 + 58752578 58752578 58752578 CGGTAAGCAGATCATTTGAACCCAGGAGTTTGAGACTAGCCTTGGCAACATGGTGAAACCCCATC CGGTAAGCAGATCATTTGAACCCAGGAGTTTGGGACTAGCCTTGGCAACATGGTGAAACCCCATC A G MALT1 Ensembl:ENSG00000172175 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1129317 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13326462 34740 RMVar_ID_34740 Human_SNP_ID_649366135 A-to-I Human chr18 + 58753226 58753226 58753226 ATTTGTTTTTTTGTTGTTGTCTTTTGAGTCTCACTCTGTCTCCCAGGCTGTAGTGCAGTGGCACG ATTTGTTTTTTTGTTGTTGTCTTTTGAGTCTCTCTCTGTCTCCCAGGCTGTAGTGCAGTGGCACG A T MALT1 Ensembl:ENSG00000172175 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1028506253 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17567368 34741 RMVar_ID_34741 Human_SNP_ID_649366160 A-to-I Human chr18 + 58753311 58753311 58753311 CGCCTCCCAGGTTCAAGCGATTCTCGTGCCTCAGCCCCCCGCATAGCTGGCATTACAGGCACACA CGCCTCCCAGGTTCAAGCGATTCTCGTGCCTCGGCCCCCCGCATAGCTGGCATTACAGGCACACA A G MALT1 Ensembl:ENSG00000172175 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs1248272107 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17567368 34742 RMVar_ID_34742 Human_SNP_ID_649366200 A-to-I Human chr18 + 58753481 58753481 58753481 TGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGTCACCATGCCCGGCCGGCAGTG TGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTCCAGGCGTGAGTCACCATGCCCGGCCGGCAGTG A C MALT1 Ensembl:ENSG00000172175 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs540521830 Functional Loss SNV dbSNP153 33..33 33 - - - 34743 RMVar_ID_34743 Human_SNP_ID_649397206 A-to-I Human chr18 + 58877015 58877015 58877015 CCAGGAGTTAGAGGCTGCAGTGAGCTAGGATCACACTACTGCACTTCAGCCTGGGCAACAGAGTG CCAGGAGTTAGAGGCTGCAGTGAGCTAGGATCGCACTACTGCACTTCAGCCTGGGCAACAGAGTG A G ZNF532 Ensembl:ENSG00000074657 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1138210 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32043,RMVar_hsa_circ_86662,RMVar_hsa_circ_29230,RMVar_hsa_circ_95403,RMVar_hsa_circ_190408,RMVar_hsa_circ_50902,RMVar_hsa_circ_82081,RMVar_hsa_circ_369625,RMVar_hsa_circ_190409,RMVar_hsa_circ_302973,RMVar_hsa_circ_49493,RMVar_hsa_circ_190410,RMVar_hsa_circ_190411,RMVar_hsa_circ_190412 34744 RMVar_ID_34744 Human_SNP_ID_649418377 A-to-I Human chr18 + 58957903 58957903 58957903 CCTGGCCAACATGACGAAACCCCATCTCTACTAAAAGTACAAAAATGAGCTGGGCATAGTGGCAG CCTGGCCAACATGACGAAACCCCATCTCTACTGAAAGTACAAAAATGAGCTGGGCATAGTGGCAG A G ZNF532 Ensembl:ENSG00000074657 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs955032480 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101219,RMVar_hsa_circ_29230,RMVar_hsa_circ_82081,RMVar_hsa_circ_190412,RMVar_hsa_circ_309920,RMVar_hsa_circ_341394,RMVar_hsa_circ_190425,RMVar_hsa_circ_265505,RMVar_hsa_circ_335724,RMVar_hsa_circ_41099,RMVar_hsa_circ_190427,RMVar_hsa_circ_319290,RMVar_hsa_circ_290147,RMVar_hsa_circ_102506,RMVar_hsa_circ_190431 34745 RMVar_ID_34745 Human_SNP_ID_649418378 A-to-I Human chr18 + 58957903 58957903 58957903 CCTGGCCAACATGACGAAACCCCATCTCTACTAAAAGTACAAAAATGAGCTGGGCATAGTGGCAG CCTGGCCAACATGACGAAACCCCATCTCTACTTAAAGTACAAAAATGAGCTGGGCATAGTGGCAG A T ZNF532 Ensembl:ENSG00000074657 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs955032480 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101219,RMVar_hsa_circ_29230,RMVar_hsa_circ_82081,RMVar_hsa_circ_190412,RMVar_hsa_circ_309920,RMVar_hsa_circ_341394,RMVar_hsa_circ_190425,RMVar_hsa_circ_265505,RMVar_hsa_circ_335724,RMVar_hsa_circ_41099,RMVar_hsa_circ_190427,RMVar_hsa_circ_319290,RMVar_hsa_circ_290147,RMVar_hsa_circ_102506,RMVar_hsa_circ_190431 34746 RMVar_ID_34746 Human_SNP_ID_649419400 A-to-I Human chr18 + 58962145 58962145 58962145 CTACTCAGGAGGCTGAGGCAGGAGAATTGTTTAAACCCGGGAGGTGAAGGTTGCGGTGAGCCGAG CTACTCAGGAGGCTGAGGCAGGAGAATTGTTTGAACCCGGGAGGTGAAGGTTGCGGTGAGCCGAG A G ZNF532 Ensembl:ENSG00000074657 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs376583852 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101219,RMVar_hsa_circ_29230,RMVar_hsa_circ_82081,RMVar_hsa_circ_190412,RMVar_hsa_circ_309920,RMVar_hsa_circ_341394,RMVar_hsa_circ_190425,RMVar_hsa_circ_265505,RMVar_hsa_circ_335724,RMVar_hsa_circ_41099,RMVar_hsa_circ_190427,RMVar_hsa_circ_319290,RMVar_hsa_circ_290147,RMVar_hsa_circ_102506,RMVar_hsa_circ_190431 34747 RMVar_ID_34747 Human_SNP_ID_649424164 A-to-I Human chr18 + 58980862 58980862 58980862 CAGAGTTTCTCCATGTTTGTCAGGCTCATCTCAAACTTCCGACCTCAGGTGATCTGCCTGCCTCG CAGAGTTTCTCCATGTTTGTCAGGCTCATCTCGAACTTCCGACCTCAGGTGATCTGCCTGCCTCG A G ZNF532 Ensembl:ENSG00000074657 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs190533313 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13326543 RMVar_hsa_circ_101219,RMVar_hsa_circ_309920,RMVar_hsa_circ_190425,RMVar_hsa_circ_265505,RMVar_hsa_circ_190427,RMVar_hsa_circ_319290,RMVar_hsa_circ_290147,RMVar_hsa_circ_318690 34748 RMVar_ID_34748 Human_SNP_ID_649511456 A-to-I Human chr18 - 59329953 59329953 59329953 AAGGAGTTTTTATAGTCTTTGTGCATACTTCTAGGTATTACAGAAACAGTCTGTAAATGACATTT AAGGAGTTTTTATAGTCTTTGTGCATACTTCTTGGTATTACAGAAACAGTCTGTAAATGACATTT T A LMAN1 Ensembl:ENSG00000074695 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1043325 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3558221,Human_RBP_ID_6698105,Human_RBP_ID_8827907,Human_RBP_ID_18300186,Human_RBP_ID_20296340,Human_RBP_ID_22390686,Human_RBP_ID_23775101,Human_RBP_ID_26462771 Human_miRNA_ID_1130295,Human_miRNA_ID_2648596,Human_miRNA_ID_2671193,Human_miRNA_ID_3101843 RMVar_hsa_circ_117284,RMVar_hsa_circ_190440,RMVar_hsa_circ_112263,RMVar_hsa_circ_190439 34749 RMVar_ID_34749 Human_SNP_ID_649511457 A-to-I Human chr18 - 59329953 59329953 59329953 AAGGAGTTTTTATAGTCTTTGTGCATACTTCTAGGTATTACAGAAACAGTCTGTAAATGACATTT AAGGAGTTTTTATAGTCTTTGTGCATACTTCTGGGTATTACAGAAACAGTCTGTAAATGACATTT T C LMAN1 Ensembl:ENSG00000074695 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1043325 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3558221,Human_RBP_ID_6698105,Human_RBP_ID_8827907,Human_RBP_ID_18300186,Human_RBP_ID_20296340,Human_RBP_ID_22390686,Human_RBP_ID_23775101,Human_RBP_ID_26462771 Human_miRNA_ID_1130295,Human_miRNA_ID_2648596,Human_miRNA_ID_2671193,Human_miRNA_ID_3101843 RMVar_hsa_circ_117284,RMVar_hsa_circ_190440,RMVar_hsa_circ_112263,RMVar_hsa_circ_190439 34750 RMVar_ID_34750 Human_SNP_ID_649511612 A-to-I Human chr18 - 59330704 59330704 59330704 CCTCATGCCTCCCAGAATATGAGGTCTAATTAAGAAGTCCCATCAGGTTTATTTTGTAACCAAAG CCTCATGCCTCCCAGAATATGAGGTCTAATTAGGAAGTCCCATCAGGTTTATTTTGTAACCAAAG T C LMAN1 Ensembl:ENSG00000074695 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs947806582 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_510075,Human_RBP_ID_1877272,Human_RBP_ID_8194393,Human_RBP_ID_22390698,Human_RBP_ID_24482975 RMVar_hsa_circ_117284,RMVar_hsa_circ_190440,RMVar_hsa_circ_112263,RMVar_hsa_circ_190439 34751 RMVar_ID_34751 Human_SNP_ID_263706214 A-to-I Human chr5 - 180033590 180033590 180033590 CTGGGTTCAAGTGAAAGTGATTCTCCTGCCTCAGACTCCCGAGCAGCTGGGATTATAGGCGCACA CTGGGTTCAAGTGAAAGTGATTCTCCTGCCTCTGACTCCCGAGCAGCTGGGATTATAGGCGCACA T A RNF130 Ensembl:ENSG00000113269 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1419916110 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96706,RMVar_hsa_circ_236712,RMVar_hsa_circ_271088,RMVar_hsa_circ_236717,RMVar_hsa_circ_236718,RMVar_hsa_circ_2315,RMVar_hsa_circ_360343 34752 RMVar_ID_34752 Human_SNP_ID_263751475 A-to-I Human chr5 - 180196462 180196462 180196462 CAGAGTCTCACTGTTGCCCAGGCTGGAGTGCAATGGTGTGATCTCGGCTCACTGCAACCTCCTCC CAGAGTCTCACTGTTGCCCAGGCTGGAGTGCAGTGGTGTGATCTCGGCTCACTGCAACCTCCTCC T C RASGEF1C Ensembl:ENSG00000146090 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1330906068 Functional Loss SNV dbSNP153 33..33 33 - - - 34753 RMVar_ID_34753 Human_SNP_ID_263764253 A-to-I Human chr5 - 180243883 180243883 180243883 AGATCATGCCACTGCACTCCAGCCTGGGCGACAGAGCGAGACTCTGTCTTTATTTATATATGTAT AGATCATGCCACTGCACTCCAGCCTGGGCGACGGAGCGAGACTCTGTCTTTATTTATATATGTAT T C MAPK9 Ensembl:ENSG00000050748 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270471411 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7424709 RMVar_hsa_circ_13130,RMVar_hsa_circ_347734,RMVar_hsa_circ_98393,RMVar_hsa_circ_236723,RMVar_hsa_circ_236724,RMVar_hsa_circ_11705,RMVar_hsa_circ_236725,RMVar_hsa_circ_372760,RMVar_hsa_circ_74354,RMVar_hsa_circ_343753 34754 RMVar_ID_34754 Human_SNP_ID_263764303 A-to-I Human chr5 - 180244027 180244027 180244027 CTGGCCAACATGGCGAAACCCCATCTCTACTAAAAATAACAAAAATTAGCCGACCGTTATGGCAG CTGGCCAACATGGCGAAACCCCATCTCTACTACAAATAACAAAAATTAGCCGACCGTTATGGCAG T G MAPK9 Ensembl:ENSG00000050748 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1417035058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8612641 RMVar_hsa_circ_13130,RMVar_hsa_circ_347734,RMVar_hsa_circ_98393,RMVar_hsa_circ_236723,RMVar_hsa_circ_236724,RMVar_hsa_circ_11705,RMVar_hsa_circ_236725,RMVar_hsa_circ_372760,RMVar_hsa_circ_74354,RMVar_hsa_circ_343753 34755 RMVar_ID_34755 Human_SNP_ID_263766896 A-to-I Human chr5 - 180254055 180254055 180254055 GACTGAGGCAGGAGAATTTCTTGAACCCAGGAAGCGGAGGTTGCAGTGAGCTGAGATAGTGCCAT GACTGAGGCAGGAGAATTTCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCTGAGATAGTGCCAT T C MAPK9 Ensembl:ENSG00000050748 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1218686745 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13130,RMVar_hsa_circ_347734,RMVar_hsa_circ_236724,RMVar_hsa_circ_236726,RMVar_hsa_circ_11705,RMVar_hsa_circ_236725,RMVar_hsa_circ_372760,RMVar_hsa_circ_270713,RMVar_hsa_circ_290126,RMVar_hsa_circ_343753,RMVar_hsa_circ_236727 34756 RMVar_ID_34756 Human_SNP_ID_263766921 A-to-I Human chr5 - 180254160 180254160 180254160 GAGTTCGACACCAGCCTGGTCAACATGGTGAAACTCTGTCTCTACTAAAAATATAAAAATTAGCT GAGTTCGACACCAGCCTGGTCAACATGGTGAATCTCTGTCTCTACTAAAAATATAAAAATTAGCT T A MAPK9 Ensembl:ENSG00000050748 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs911845264 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13130,RMVar_hsa_circ_347734,RMVar_hsa_circ_236724,RMVar_hsa_circ_236726,RMVar_hsa_circ_11705,RMVar_hsa_circ_236725,RMVar_hsa_circ_372760,RMVar_hsa_circ_270713,RMVar_hsa_circ_290126,RMVar_hsa_circ_343753,RMVar_hsa_circ_236727 34757 RMVar_ID_34757 Human_SNP_ID_263830647 A-to-I Human chr5 + 180475110 180475110 180475110 ACAGTGGCTCAGGCCTGTACTCCCAGCGCTTTAGGAGGCCAAGGTGGGCAGATCACGTGAGCCCA ACAGTGGCTCAGGCCTGTACTCCCAGCGCTTTGGGAGGCCAAGGTGGGCAGATCACGTGAGCCCA A G lnc-CNOT6-1 RNACentral:URS00008B5857 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1276917309 Functional Loss SNV dbSNP153 33..33 33 - - - 34758 RMVar_ID_34758 Human_SNP_ID_263830958 A-to-I Human chr5 + 180476179 180476179 180476179 ACGCTGGTCTCGAACTCCCGACCTTGTGATCCACCCGCTCTGGCCTCCCAGAGTCCTGGGATTAC ACGCTGGTCTCGAACTCCCGACCTTGTGATCCTCCCGCTCTGGCCTCCCAGAGTCCTGGGATTAC A T lnc-CNOT6-1 RNACentral:URS00008B5857 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1316507274 Functional Loss SNV dbSNP153 33..33 33 - - - 34759 RMVar_ID_34759 Human_SNP_ID_263834641 A-to-I Human chr5 - 180490287 180490287 180490287 ACAATCTCGGCTTGTTGCAAGCTCCACCTCCCAGATTCAAGCAATTCTCCTGCCTCAGTTTCCCG ACAATCTCGGCTTGTTGCAAGCTCCACCTCCCGGATTCAAGCAATTCTCCTGCCTCAGTTTCCCG 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 GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1422108626 Functional Loss SNV dbSNP153 33..33 33 - - - 34760 RMVar_ID_34760 Human_SNP_ID_263839880 A-to-I Human chr5 + 180508453 180508453 180508453 CCTGCCTCAGCCTCCTGGGTGGCTGGGACTACAGGCGCACGCCACCATGCCCAGCTAATTTTTGT CCTGCCTCAGCCTCCTGGGTGGCTGGGACTACCGGCGCACGCCACCATGCCCAGCTAATTTTTGT A C CNOT6 Ensembl:ENSG00000113300 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs993992124 Functional Loss SNV dbSNP153 33..33 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 34761 RMVar_ID_34761 Human_SNP_ID_263839881 A-to-I Human chr5 + 180508453 180508453 180508453 CCTGCCTCAGCCTCCTGGGTGGCTGGGACTACAGGCGCACGCCACCATGCCCAGCTAATTTTTGT CCTGCCTCAGCCTCCTGGGTGGCTGGGACTACGGGCGCACGCCACCATGCCCAGCTAATTTTTGT A G CNOT6 Ensembl:ENSG00000113300 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs993992124 Functional Loss SNV dbSNP153 33..33 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 34762 RMVar_ID_34762 Human_SNP_ID_263841646 A-to-I Human chr5 + 180514301 180514301 180514301 AAAATCAGCCACATGTGTTGGGGGGCGCCTGTAATCCCATCTACTCGGGAGGCTGAGGCAGGAGA AAAATCAGCCACATGTGTTGGGGGGCGCCTGTCATCCCATCTACTCGGGAGGCTGAGGCAGGAGA A C CNOT6 Ensembl:ENSG00000113300 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs557378214 Functional Loss SNV dbSNP153 33..33 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 34763 RMVar_ID_34763 Human_SNP_ID_263841651 A-to-I Human chr5 + 180514311 180514311 180514311 ACATGTGTTGGGGGGCGCCTGTAATCCCATCTACTCGGGAGGCTGAGGCAGGAGAATTGCTTGAA ACATGTGTTGGGGGGCGCCTGTAATCCCATCTGCTCGGGAGGCTGAGGCAGGAGAATTGCTTGAA A G CNOT6 Ensembl:ENSG00000113300 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1365302426 Functional Loss SNV dbSNP153 33..33 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 34764 RMVar_ID_34764 Human_SNP_ID_263847046 A-to-I Human chr5 - 180534316 180534316 180534316 ACAATGTTGAGAAAGAAAACCACTCCAAAATCATCGCAGGGGTACTGGGCCTAATTGCTAAGGGC ACAATGTTGAGAAAGAAAACCACTCCAAAATCGTCGCAGGGGTACTGGGCCTAATTGCTAAGGGC T C AC122714.1 Ensembl:ENSG00000250749 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049208837 Functional Loss SNV dbSNP153 33..33 33 - - - 34765 RMVar_ID_34765 Human_SNP_ID_263852360 A-to-I Human chr5 + 180552384 180552384 180552384 CAAATAGGCTGGGCACGATGGCTCAAGCCTATAATCCCAGCACACTTTGGGAGGCCGAGGCGGGC CAAATAGGCTGGGCACGATGGCTCAAGCCTATTATCCCAGCACACTTTGGGAGGCCGAGGCGGGC A T CNOT6 Ensembl:ENSG00000113300 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1418084022 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33719,RMVar_hsa_circ_281788,RMVar_hsa_circ_236744,RMVar_hsa_circ_236745,RMVar_hsa_circ_332998,RMVar_hsa_circ_353348,RMVar_hsa_circ_236748,RMVar_hsa_circ_236747,RMVar_hsa_circ_236749,RMVar_hsa_circ_236753,RMVar_hsa_circ_284135,RMVar_hsa_circ_320393,RMVar_hsa_circ_372611,RMVar_hsa_circ_280449,RMVar_hsa_circ_236755,RMVar_hsa_circ_236754,RMVar_hsa_circ_236751,RMVar_hsa_circ_236752,RMVar_hsa_circ_236750 34766 RMVar_ID_34766 Human_SNP_ID_263853661 A-to-I Human chr5 + 180556835 180556835 180556835 AAAATTAGCCAGGCATGGTGGCAGGTGCCTGTAGTCCCAGCTACTCGGGAGACTGAGGTGGGAGA AAAATTAGCCAGGCATGGTGGCAGGTGCCTGTGGTCCCAGCTACTCGGGAGACTGAGGTGGGAGA A G CNOT6 Ensembl:ENSG00000113300 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1448488877 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33719,RMVar_hsa_circ_236745,RMVar_hsa_circ_332998,RMVar_hsa_circ_353348,RMVar_hsa_circ_236748,RMVar_hsa_circ_236749,RMVar_hsa_circ_236753,RMVar_hsa_circ_284135,RMVar_hsa_circ_320393,RMVar_hsa_circ_372611,RMVar_hsa_circ_236751,RMVar_hsa_circ_236752,RMVar_hsa_circ_236750,RMVar_hsa_circ_66932,RMVar_hsa_circ_321622,RMVar_hsa_circ_376831,RMVar_hsa_circ_298864,RMVar_hsa_circ_236758 34767 RMVar_ID_34767 Human_SNP_ID_263866495 A-to-I Human chr5 - 180602505 180602504 180602505 GGTGTTGAGAGCCATCCTGCAAGTCTTTTTCAACAGAACTTCACAGACTGTTAGAGCTGCTGAGA GGTGTTGAGAGCCATCCTGCAAGTCTTTTTCA_CAGAACTTCACAGACTGTTAGAGCTGCTGAGA GT G FLT4 Ensembl:ENSG00000037280 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1291061122 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_18357498 34768 RMVar_ID_34768 Human_SNP_ID_263921124 A-to-I Human chr5 - 180795798 180795797 180795798 ACCGAGGAATTCAGGGCAAACAGATCATCTCAATTTGCCTTGCTGATGTGCCAGCTGGGATTACG ACCGAGGAATTCAGGGCAAACAGATCATCTCA_TTTGCCTTGCTGATGTGCCAGCTGGGATTACG AT A MGAT1 Ensembl:ENSG00000131446 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-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 34769 RMVar_ID_34769 Human_SNP_ID_263921125 A-to-I Human chr5 - 180795798 180795798 180795798 ACCGAGGAATTCAGGGCAAACAGATCATCTCAATTTGCCTTGCTGATGTGCCAGCTGGGATTACG ACCGAGGAATTCAGGGCAAACAGATCATCTCAGTTTGCCTTGCTGATGTGCCAGCTGGGATTACG T C MGAT1 Ensembl:ENSG00000131446 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-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 34770 RMVar_ID_34770 Human_SNP_ID_263921313 A-to-I Human chr5 - 180796560 180796554 180796560 GCATCACTCTTTTCTTCCACATAAACTTTCTTAAAAATCAAATATGGGGATATGGCCCACAGCTC GCATCACTCTTTTCTTCCACATAAACTTTCTT______CAAATATGGGGATATGGCCCACAGCTC GATTTTT G MGAT1 Ensembl:ENSG00000131446 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1407368258 Functional Loss DEL dbSNP153 33..38 33 - - - RMVar_hsa_circ_120765,RMVar_hsa_circ_236769 34771 RMVar_ID_34771 Human_SNP_ID_263921494 A-to-I Human chr5 - 180797302 180797302 180797302 CGCCTCCCAGGTTCAAGGGATTCTCCTGTCTCAGCCTTCTGAGTAGCTGGGATTACAGGCACGCA CGCCTCCCAGGTTCAAGGGATTCTCCTGTCTCCGCCTTCTGAGTAGCTGGGATTACAGGCACGCA T G MGAT1 Ensembl:ENSG00000131446 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1186279961 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120765,RMVar_hsa_circ_236769 34772 RMVar_ID_34772 Human_SNP_ID_263931965 A-to-I Human chr5 + 180833219 180833219 180833219 AATGACTGCCTAAGAGAACAGAGATGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGT AATGACTGCCTAAGAGAACAGAGATGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGT A G LINC00847 Ensembl:ENSG00000245060 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs952193589 Functional Loss SNV dbSNP153 33..33 33 - - - 34773 RMVar_ID_34773 Human_SNP_ID_263932549 A-to-I Human chr5 + 180835372 180835372 180835372 GACACTTGCACCAGTGGCCCTCTGGGGCTCTCAAGCCTTTAGCCTTGAACTTAGTTACACCATGT GACACTTGCACCAGTGGCCCTCTGGGGCTCTCGAGCCTTTAGCCTTGAACTTAGTTACACCATGT A G LINC00847 Ensembl:ENSG00000245060 lincRNA intron GSE100210;GSE99789;GSE107867;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490832,GSM3490833,GSM3490834;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,EC109;ASD brains,Fragile X samples from NIH NeuroBioBank;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,KYSE180 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,29796672,30559470,31158229,32596459,32596459 RNA-Seq:(High) rs1242812298 Functional Loss SNV dbSNP153 33..33 33 - - - 34774 RMVar_ID_34774 Human_SNP_ID_264027259 A-to-I Human chr5 + 181207340 181207340 181207340 TGAGGCAGGAGAAGTGCTTGAATCCAGGAGGCAGAGGTTGCAGTGAACCGAGATTGCGCCACGAC TGAGGCAGGAGAAGTGCTTGAATCCAGGAGGCGGAGGTTGCAGTGAACCGAGATTGCGCCACGAC A G RF00017-049 RNACentral:URS000096B6E3 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893588653 Functional Loss SNV dbSNP153 33..33 33 - - - 34775 RMVar_ID_34775 Human_SNP_ID_264034881 A-to-I Human chr5 + 181228673 181228673 181228673 CAGCAATTTAGGGTCCCGGCACGGTGGCTCACACCTGTAGTCCCAGCACTTTGGGAGGCAGAGGT CAGCAATTTAGGGTCCCGGCACGGTGGCTCACTCCTGTAGTCCCAGCACTTTGGGAGGCAGAGGT A T TRIM41 Ensembl:ENSG00000146063 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs998376638 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114296,RMVar_hsa_circ_236774 34776 RMVar_ID_34776 Human_SNP_ID_264037978 A-to-I Human chr5 - 181237170 181237170 181237170 AGGGGCTTAAGGCTGTAGTGAGCCAGGATCGCACCCCTGCACTCCAGCCTAGACAATGGAGCAAG AGGGGCTTAAGGCTGTAGTGAGCCAGGATCGCTCCCCTGCACTCCAGCCTAGACAATGGAGCAAG T A RACK1 Ensembl:ENSG00000204628 Protein coding intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1357505456 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_640639,Human_RBP_ID_1391293,Human_RBP_ID_1652916,Human_RBP_ID_15417073,Human_RBP_ID_23044163 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_83853,RMVar_hsa_circ_236776,RMVar_hsa_circ_236778,RMVar_hsa_circ_236780,RMVar_hsa_circ_236782,RMVar_hsa_circ_236781,RMVar_hsa_circ_236779,RMVar_hsa_circ_236777 34777 RMVar_ID_34777 Human_SNP_ID_264039336 A-to-I Human chr5 - 181240779 181240779 181240779 TCACGCCTGTAATCCTAGCTCTCTGGTAGGCCAAGGTGGGAGGACTGCTTGAGGACAGGAGAGCA TCACGCCTGTAATCCTAGCTCTCTGGTAGGCCGAGGTGGGAGGACTGCTTGAGGACAGGAGAGCA T C RACK1 Ensembl:ENSG00000204628 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1245717928 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2217315,Human_miRNA_ID_2867534 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 34778 RMVar_ID_34778 Human_SNP_ID_264039379 A-to-I Human chr5 - 181240885 181240885 181240885 ACCTCAGGTGATCTGCCCGCCTCAGCCTCCCAAAGTGCTGGGATTATAAGCGTGAGCCACCGTCC ACCTCAGGTGATCTGCCCGCCTCAGCCTCCCAGAGTGCTGGGATTATAAGCGTGAGCCACCGTCC T C RACK1 Ensembl:ENSG00000204628 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs536318381 Functional Loss SNV dbSNP153 33..33 33 - - - 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 34779 RMVar_ID_34779 Human_SNP_ID_264039380 A-to-I Human chr5 - 181240885 181240885 181240885 ACCTCAGGTGATCTGCCCGCCTCAGCCTCCCAAAGTGCTGGGATTATAAGCGTGAGCCACCGTCC ACCTCAGGTGATCTGCCCGCCTCAGCCTCCCACAGTGCTGGGATTATAAGCGTGAGCCACCGTCC T G RACK1 Ensembl:ENSG00000204628 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs536318381 Functional Loss SNV dbSNP153 33..33 33 - - - 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 34780 RMVar_ID_34780 Human_SNP_ID_264039696 A-to-I Human chr5 - 181241752 181241751 181241752 ACTCAGTCACTTGACTCTGTGATCAGAGCCAAATCCAGGGTTGTATGAGTGATGCAATGAGACAG ACTCAGTCACTTGACTCTGTGATCAGAGCCAA_TCCAGGGTTGTATGAGTGATGCAATGAGACAG AT A RACK1 Ensembl:ENSG00000204628 Protein coding intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1488030573 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_1652970,Human_RBP_ID_1993972,Human_RBP_ID_8267544,Human_RBP_ID_15417329,Human_RBP_ID_24101936 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_236807,RMVar_hsa_circ_82079,RMVar_hsa_circ_236810,RMVar_hsa_circ_236811,RMVar_hsa_circ_236809 34781 RMVar_ID_34781 Human_SNP_ID_264040508 A-to-I Human chr5 - 181243863 181243863 181243863 TGCAAGGCGGCGGCAGGAGAGGTTGTGGTGCTAGTTTCTCTAAGCCATCCAGTGCCATCCTCGTC TGCAAGGCGGCGGCAGGAGAGGTTGTGGTGCTGGTTTCTCTAAGCCATCCAGTGCCATCCTCGTC T C RACK1 Ensembl:ENSG00000204628 Protein coding 5'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1293793921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250504,Human_RBP_ID_640683,Human_RBP_ID_1041133,Human_RBP_ID_1212403,Human_RBP_ID_1321140,Human_RBP_ID_1653004,Human_RBP_ID_1993991,Human_RBP_ID_3767522,Human_RBP_ID_4846263,Human_RBP_ID_5242346,Human_RBP_ID_5476635,Human_RBP_ID_5509474,Human_RBP_ID_7426038,Human_RBP_ID_8613019,Human_RBP_ID_9175574,Human_RBP_ID_9335548,Human_RBP_ID_15417444,Human_RBP_ID_17415509,Human_RBP_ID_17532265,Human_RBP_ID_17662335,Human_RBP_ID_18195216,Human_RBP_ID_18840772,Human_RBP_ID_21218233,Human_RBP_ID_22100589,Human_RBP_ID_22300326,Human_RBP_ID_22459467,Human_RBP_ID_22512267,Human_RBP_ID_22828332,Human_RBP_ID_23137016,Human_RBP_ID_24101982,Human_RBP_ID_24432619,Human_RBP_ID_24506028,Human_RBP_ID_26702003,Human_RBP_ID_26826998,Human_RBP_ID_27080921,Human_RBP_ID_27336055,Human_RBP_ID_27515251 Human_miRNA_ID_2042674,Human_miRNA_ID_2044825,Human_miRNA_ID_2299866,Human_miRNA_ID_2303134,Human_miRNA_ID_2306398 RMVar_hsa_circ_83853,RMVar_hsa_circ_236789,RMVar_hsa_circ_236776,RMVar_hsa_circ_90860,RMVar_hsa_circ_44697,RMVar_hsa_circ_236790,RMVar_hsa_circ_77061,RMVar_hsa_circ_236796,RMVar_hsa_circ_110756,RMVar_hsa_circ_83006,RMVar_hsa_circ_236801,RMVar_hsa_circ_79325,RMVar_hsa_circ_87613,RMVar_hsa_circ_236806,RMVar_hsa_circ_82079,RMVar_hsa_circ_100156,RMVar_hsa_circ_236810,RMVar_hsa_circ_236811,RMVar_hsa_circ_95427,RMVar_hsa_circ_236813,RMVar_hsa_circ_236815 34782 RMVar_ID_34782 Human_SNP_ID_264041905 A-to-I Human chr5 + 181248737 181248705 181248738 AGAGTAGTTTCTTTAAGAGTCTGATCTCGGCCAGGCGCAGTGGCTCACGCCTGTAATCCCAGTAC A_________________________________GCGCAGTGGCTCACGCCTGTAATCCCAGTAC AGAGTAGTTTCTTTAAGAGTCTGATCTCGGCCAG A AC008443.1 Ensembl:ENSG00000233937 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1306152959 Functional Loss DEL dbSNP153 2..34 33 - - - 34783 RMVar_ID_34783 Human_SNP_ID_264041916 A-to-I Human chr5 + 181248737 181248737 181248737 AGAGTAGTTTCTTTAAGAGTCTGATCTCGGCCAGGCGCAGTGGCTCACGCCTGTAATCCCAGTAC AGAGTAGTTTCTTTAAGAGTCTGATCTCGGCCTGGCGCAGTGGCTCACGCCTGTAATCCCAGTAC A T AC008443.1 Ensembl:ENSG00000233937 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs962711339 Functional Loss SNV dbSNP153 33..33 33 - - - 34784 RMVar_ID_34784 Human_SNP_ID_264041921 A-to-I Human chr5 + 181248743 181248743 181248743 GTTTCTTTAAGAGTCTGATCTCGGCCAGGCGCAGTGGCTCACGCCTGTAATCCCAGTACTTCGGA GTTTCTTTAAGAGTCTGATCTCGGCCAGGCGCGGTGGCTCACGCCTGTAATCCCAGTACTTCGGA A G AC008443.1 Ensembl:ENSG00000233937 lincRNA intron GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs1336250994 Functional Loss SNV dbSNP153 33..33 33 - - - 34785 RMVar_ID_34785 Human_SNP_ID_264043187 A-to-I Human chr5 + 181254215 181254215 181254215 GGCAGGCTGAGGCAGGAGAATGGCATGAATCCAGGAGGCGGAGCTGGCAGTGAGCCGAGATCGTG GGCAGGCTGAGGCAGGAGAATGGCATGAATCCCGGAGGCGGAGCTGGCAGTGAGCCGAGATCGTG A C AC008443.1 Ensembl:ENSG00000233937 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1329717082 Functional Loss SNV dbSNP153 33..33 33 - - - 34786 RMVar_ID_34786 Human_SNP_ID_264043251 A-to-I Human chr5 + 181254398 181254397 181254399 TTGTTGTTGTTGTTGTTGTTTCCCCCGCAGACAGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCA TTGTTGTTGTTGTTGTTGTTTCCCCCGCAGAC__AGTCTCGCTCTGTCGCCCAGGCTGGAGTGCA CAG C AC008443.1 Ensembl:ENSG00000233937 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1414593951 Functional Loss DEL dbSNP153 33..34 33 - - - 34787 RMVar_ID_34787 Human_SNP_ID_525464023 A-to-I Human chr13 - 30229596 30229594 30229597 CTCCTGCCTCAGCCTCCTAAGTAGCTGGGACCACAGGCACATGCCACCACATCTGGCTAAGTTTT CTCCTGCCTCAGCCTCCTAAGTAGCTGGGAC___AGGCACATGCCACCACATCTGGCTAAGTTTT TGTG T KATNAL1 Ensembl:ENSG00000102781 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1321943155 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_48251,RMVar_hsa_circ_100667,RMVar_hsa_circ_162518,RMVar_hsa_circ_162516,RMVar_hsa_circ_162520,RMVar_hsa_circ_162517,RMVar_hsa_circ_162521,RMVar_hsa_circ_162519,RMVar_hsa_circ_162522,RMVar_hsa_circ_162524,RMVar_hsa_circ_10720,RMVar_hsa_circ_273955,RMVar_hsa_circ_289487,RMVar_hsa_circ_311807,RMVar_hsa_circ_271384,RMVar_hsa_circ_162526,RMVar_hsa_circ_162527,RMVar_hsa_circ_162525,RMVar_hsa_circ_162523 34788 RMVar_ID_34788 Human_SNP_ID_525469692 A-to-I Human chr13 - 30252884 30252884 30252884 AAATTAGCTGGGTGTGGTGGTGCATGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCATGAGAA AAATTAGCTGGGTGTGGTGGTGCATGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCATGAGAA T C KATNAL1 Ensembl:ENSG00000102781 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs971668514 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_162518,RMVar_hsa_circ_162520,RMVar_hsa_circ_162519,RMVar_hsa_circ_162522,RMVar_hsa_circ_98678,RMVar_hsa_circ_10720,RMVar_hsa_circ_273955,RMVar_hsa_circ_311807,RMVar_hsa_circ_162526,RMVar_hsa_circ_162527,RMVar_hsa_circ_162525,RMVar_hsa_circ_162531,RMVar_hsa_circ_315407,RMVar_hsa_circ_366410,RMVar_hsa_circ_162530,RMVar_hsa_circ_365097,RMVar_hsa_circ_162532,RMVar_hsa_circ_162534,RMVar_hsa_circ_162535 34789 RMVar_ID_34789 Human_SNP_ID_525481479 A-to-I Human chr13 - 30296407 30296407 30296407 GGGCCCAAGCCTCCCTCCTTCCGGGGGATGTTAATCCAAGCCAGGTGGGTGAACTGAGAGTCCAC GGGCCCAAGCCTCCCTCCTTCCGGGGGATGTTGATCCAAGCCAGGTGGGTGAACTGAGAGTCCAC T C KATNAL1 Ensembl:ENSG00000102781 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1158446626 Functional Loss SNV dbSNP153 33..33 33 - - - 34790 RMVar_ID_34790 Human_SNP_ID_525481480 A-to-I Human chr13 - 30296412 30296412 30296412 TCAGGGGGCCCAAGCCTCCCTCCTTCCGGGGGATGTTAATCCAAGCCAGGTGGGTGAACTGAGAG TCAGGGGGCCCAAGCCTCCCTCCTTCCGGGGGGTGTTAATCCAAGCCAGGTGGGTGAACTGAGAG T C KATNAL1 Ensembl:ENSG00000102781 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1438284894 Functional Loss SNV dbSNP153 33..33 33 - - - 34791 RMVar_ID_34791 Human_SNP_ID_525482738 A-to-I Human chr13 - 30302117 30302117 30302117 TTATCCCAGCACTTTGGGAGGCTGAGAGGGGCAGAAAGCTTGAGTCCAGGAGTTTGAGACAAGTT TTATCCCAGCACTTTGGGAGGCTGAGAGGGGCCGAAAGCTTGAGTCCAGGAGTTTGAGACAAGTT T G KATNAL1 Ensembl:ENSG00000102781 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1220341521 Functional Loss SNV dbSNP153 33..33 33 - - - 34792 RMVar_ID_34792 Human_SNP_ID_525495553 A-to-I Human chr13 - 30356679 30356679 30356679 GGCTCAAGCCATCCTCCCACCTCAGCCTCTCAAGTAGCTGGGACTACAGGTGTGTGTCCCCATGC GGCTCAAGCCATCCTCCCACCTCAGCCTCTCAGGTAGCTGGGACTACAGGTGTGTGTCCCCATGC T C LINC00426 Ensembl:ENSG00000238121 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1000387379 Functional Loss SNV dbSNP153 33..33 33 - - - 34793 RMVar_ID_34793 Human_SNP_ID_525495622 A-to-I Human chr13 - 30356952 30356952 30356952 CTCCCACCTCAGCCTCCTGAGTAGCTGGGACTACAGGCATACACCACCATGTCTGGCTAAATTTT CTCCCACCTCAGCCTCCTGAGTAGCTGGGACTGCAGGCATACACCACCATGTCTGGCTAAATTTT T C LINC00426 Ensembl:ENSG00000238121 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1339660222 Functional Loss SNV dbSNP153 33..33 33 - - - 34794 RMVar_ID_34794 Human_SNP_ID_525495628 A-to-I Human chr13 - 30356974 30356974 30356974 GACCTCCTGGGTTCAAGCCATCCTCCCACCTCAGCCTCCTGAGTAGCTGGGACTACAGGCATACA GACCTCCTGGGTTCAAGCCATCCTCCCACCTCGGCCTCCTGAGTAGCTGGGACTACAGGCATACA T C LINC00426 Ensembl:ENSG00000238121 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1312051150 Functional Loss SNV dbSNP153 33..33 33 - - - 34795 RMVar_ID_34795 Human_SNP_ID_525495711 A-to-I Human chr13 - 30357350 30357350 30357350 TGGCCGGAGTTTAAGGATTTGGGGCTGGGCACAGTGGCTCGTGCCTGTAATCCTAGCACTTTGGG TGGCCGGAGTTTAAGGATTTGGGGCTGGGCACTGTGGCTCGTGCCTGTAATCCTAGCACTTTGGG T A LINC00426 Ensembl:ENSG00000238121 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1258456766 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1453504 34796 RMVar_ID_34796 Human_SNP_ID_525495712 A-to-I Human chr13 - 30357350 30357350 30357350 TGGCCGGAGTTTAAGGATTTGGGGCTGGGCACAGTGGCTCGTGCCTGTAATCCTAGCACTTTGGG TGGCCGGAGTTTAAGGATTTGGGGCTGGGCACGGTGGCTCGTGCCTGTAATCCTAGCACTTTGGG T C LINC00426 Ensembl:ENSG00000238121 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1258456766 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1453504 34797 RMVar_ID_34797 Human_SNP_ID_525498192 A-to-I Human chr13 - 30367604 30367604 30367604 CTTCTGCTTCAGCGTCCCAAGTAGCTGGGATTACAGGTGAGCACCATCATGCCTGGCTAATTTTG CTTCTGCTTCAGCGTCCCAAGTAGCTGGGATTGCAGGTGAGCACCATCATGCCTGGCTAATTTTG T C LINC00426 Ensembl:ENSG00000238121 lincRNA exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1358718680 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1453463,Human_Splice_Rec_1453473,Human_Splice_Rec_1453525 RMVar_hsa_circ_69722 34798 RMVar_ID_34798 Human_SNP_ID_525498201 A-to-I Human chr13 - 30367639 30367638 30367639 TCATTATAACCTCCGCCTCCCGGGTTCAAGCAATTCTTCTGCTTCAGCGTCCCAAGTAGCTGGGA TCATTATAACCTCCGCCTCCCGGGTTCAAGCA_TTCTTCTGCTTCAGCGTCCCAAGTAGCTGGGA AT A LINC00426 Ensembl:ENSG00000238121 lincRNA exon GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1415428025 Functional Loss DEL dbSNP153 33..33 33 - - - Human_Splice_Rec_1453463,Human_Splice_Rec_1453472,Human_Splice_Rec_1453473,Human_Splice_Rec_1453524,Human_Splice_Rec_1453525 RMVar_hsa_circ_69722 34799 RMVar_ID_34799 Human_SNP_ID_525498202 A-to-I Human chr13 - 30367639 30367639 30367639 TCATTATAACCTCCGCCTCCCGGGTTCAAGCAATTCTTCTGCTTCAGCGTCCCAAGTAGCTGGGA TCATTATAACCTCCGCCTCCCGGGTTCAAGCAGTTCTTCTGCTTCAGCGTCCCAAGTAGCTGGGA T C LINC00426 Ensembl:ENSG00000238121 lincRNA exon GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1403939429 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1453463,Human_Splice_Rec_1453472,Human_Splice_Rec_1453473,Human_Splice_Rec_1453524,Human_Splice_Rec_1453525 RMVar_hsa_circ_69722 34800 RMVar_ID_34800 Human_SNP_ID_525498203 A-to-I Human chr13 - 30367640 30367640 30367640 CTCATTATAACCTCCGCCTCCCGGGTTCAAGCAATTCTTCTGCTTCAGCGTCCCAAGTAGCTGGG CTCATTATAACCTCCGCCTCCCGGGTTCAAGCGATTCTTCTGCTTCAGCGTCCCAAGTAGCTGGG T C LINC00426 Ensembl:ENSG00000238121 lincRNA exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs933342462 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1453463,Human_Splice_Rec_1453472,Human_Splice_Rec_1453473,Human_Splice_Rec_1453524,Human_Splice_Rec_1453525 RMVar_hsa_circ_69722 34801 RMVar_ID_34801 Human_SNP_ID_525498214 A-to-I Human chr13 - 30367666 30367666 30367666 CCTAGAGTGCAATGGCGCTATTTCGGCTCATTATAACCTCCGCCTCCCGGGTTCAAGCAATTCTT CCTAGAGTGCAATGGCGCTATTTCGGCTCATTGTAACCTCCGCCTCCCGGGTTCAAGCAATTCTT T C LINC00426 Ensembl:ENSG00000238121 lincRNA exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs552200672 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1453463,Human_Splice_Rec_1453472,Human_Splice_Rec_1453473,Human_Splice_Rec_1453524,Human_Splice_Rec_1453525 RMVar_hsa_circ_69722 34802 RMVar_ID_34802 Human_SNP_ID_525498222 A-to-I Human chr13 - 30367687 30367687 30367687 AGCGTTTCACTCGTCGCCCAGCCTAGAGTGCAATGGCGCTATTTCGGCTCATTATAACCTCCGCC AGCGTTTCACTCGTCGCCCAGCCTAGAGTGCAGTGGCGCTATTTCGGCTCATTATAACCTCCGCC T C LINC00426 Ensembl:ENSG00000238121 lincRNA exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1351279405 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1453463,Human_Splice_Rec_1453472,Human_Splice_Rec_1453473,Human_Splice_Rec_1453524,Human_Splice_Rec_1453525 RMVar_hsa_circ_69722 34803 RMVar_ID_34803 Human_SNP_ID_525556225 A-to-I Human chr13 - 30599733 30599733 30599733 AAGTTTAAATGAGGTCTTTATGGTGGACCCTAATCCAATATGACTAGTATCTTTATAAGAAGAGG AAGTTTAAATGAGGTCTTTATGGTGGACCCTAGTCCAATATGACTAGTATCTTTATAAGAAGAGG T C HMGB1 Ensembl:ENSG00000189403 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1384496751 Functional Loss SNV dbSNP153 33..33 33 - - - 34804 RMVar_ID_34804 Human_SNP_ID_525562415 A-to-I Human chr13 + 30624523 30624523 30624523 GTCTGTAGCCCCAGCTACCCGGGAGGGGGACTACGGGTGCACGGCACCATGCCCAGGAGGTCCAG GTCTGTAGCCCCAGCTACCCGGGAGGGGGACTCCGGGTGCACGGCACCATGCCCAGGAGGTCCAG A C USPL1 Ensembl:ENSG00000132952 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334106747 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_162547,RMVar_hsa_circ_90231,RMVar_hsa_circ_377138,RMVar_hsa_circ_376654,RMVar_hsa_circ_28746,RMVar_hsa_circ_326436,RMVar_hsa_circ_368198,RMVar_hsa_circ_162545,RMVar_hsa_circ_362749,RMVar_hsa_circ_309272,RMVar_hsa_circ_162548,RMVar_hsa_circ_162546 34805 RMVar_ID_34805 Human_SNP_ID_525562416 A-to-I Human chr13 + 30624523 30624523 30624523 GTCTGTAGCCCCAGCTACCCGGGAGGGGGACTACGGGTGCACGGCACCATGCCCAGGAGGTCCAG GTCTGTAGCCCCAGCTACCCGGGAGGGGGACTGCGGGTGCACGGCACCATGCCCAGGAGGTCCAG A G USPL1 Ensembl:ENSG00000132952 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334106747 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_162547,RMVar_hsa_circ_90231,RMVar_hsa_circ_377138,RMVar_hsa_circ_376654,RMVar_hsa_circ_28746,RMVar_hsa_circ_326436,RMVar_hsa_circ_368198,RMVar_hsa_circ_162545,RMVar_hsa_circ_362749,RMVar_hsa_circ_309272,RMVar_hsa_circ_162548,RMVar_hsa_circ_162546 34806 RMVar_ID_34806 Human_SNP_ID_525565483 A-to-I Human chr13 + 30637004 30637004 30637004 GAGCATCTCACTTGCCCAGGCTGGAGTGCAGTAGTACAATCACAGCTCACTGCAGCTTGTAGAAC GAGCATCTCACTTGCCCAGGCTGGAGTGCAGTGGTACAATCACAGCTCACTGCAGCTTGTAGAAC A G USPL1 Ensembl:ENSG00000132952 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1332153155 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12256567,Human_RBP_ID_17835981 RMVar_hsa_circ_162547,RMVar_hsa_circ_90231,RMVar_hsa_circ_377138,RMVar_hsa_circ_376654,RMVar_hsa_circ_28746,RMVar_hsa_circ_326436,RMVar_hsa_circ_162545,RMVar_hsa_circ_362749,RMVar_hsa_circ_309272,RMVar_hsa_circ_162548,RMVar_hsa_circ_162552,RMVar_hsa_circ_273432,RMVar_hsa_circ_307427,RMVar_hsa_circ_357264,RMVar_hsa_circ_316108,RMVar_hsa_circ_162553,RMVar_hsa_circ_162550,RMVar_hsa_circ_162551 34807 RMVar_ID_34807 Human_SNP_ID_525567193 A-to-I Human chr13 + 30644118 30644118 30644118 CAGCCTGGCCAACATGGTGAAACGCTGTCTCTACTGAAAATACAAAAATTAGCCGGGCATGATGG CAGCCTGGCCAACATGGTGAAACGCTGTCTCTGCTGAAAATACAAAAATTAGCCGGGCATGATGG A G USPL1 Ensembl:ENSG00000132952 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1227061637 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90231,RMVar_hsa_circ_377138,RMVar_hsa_circ_162545,RMVar_hsa_circ_362749,RMVar_hsa_circ_309272,RMVar_hsa_circ_162548,RMVar_hsa_circ_35931,RMVar_hsa_circ_162552,RMVar_hsa_circ_273432,RMVar_hsa_circ_316108,RMVar_hsa_circ_162553,RMVar_hsa_circ_283960,RMVar_hsa_circ_360551,RMVar_hsa_circ_162554,RMVar_hsa_circ_374775,RMVar_hsa_circ_162555 34808 RMVar_ID_34808 Human_SNP_ID_525567199 A-to-I Human chr13 + 30644144 30644144 30644144 GTCTCTACTGAAAATACAAAAATTAGCCGGGCATGATGGCGGACACCTGTAGTCCCAGCTACTCG GTCTCTACTGAAAATACAAAAATTAGCCGGGCGTGATGGCGGACACCTGTAGTCCCAGCTACTCG A G USPL1 Ensembl:ENSG00000132952 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1449304281 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90231,RMVar_hsa_circ_377138,RMVar_hsa_circ_162545,RMVar_hsa_circ_362749,RMVar_hsa_circ_309272,RMVar_hsa_circ_162548,RMVar_hsa_circ_35931,RMVar_hsa_circ_162552,RMVar_hsa_circ_273432,RMVar_hsa_circ_316108,RMVar_hsa_circ_162553,RMVar_hsa_circ_283960,RMVar_hsa_circ_360551,RMVar_hsa_circ_162554,RMVar_hsa_circ_374775,RMVar_hsa_circ_162555 34809 RMVar_ID_34809 Human_SNP_ID_525992420 A-to-I Human chr13 + 32335198 32335198 32335198 AAACCCCATCTCTATGAAAAAAAACAAAAATTATCCAGATGTGGTGGCATGTGCCTGTAATCCCA AAACCCCATCTCTATGAAAAAAAACAAAAATTGTCCAGATGTGGTGGCATGTGCCTGTAATCCCA A G BRCA2 Ensembl:ENSG00000139618 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1036161951 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109405,RMVar_hsa_circ_120972,RMVar_hsa_circ_362683,RMVar_hsa_circ_162618,RMVar_hsa_circ_61551,RMVar_hsa_circ_162622 34810 RMVar_ID_34810 Human_SNP_ID_525992588 A-to-I Human chr13 + 32335940 32335940 32335940 GTCTCATTCTGTTACCTAGTCTGGAGTGCACTAGTGTGATCTCAGCTCACCGTAGCCTCACCCTC GTCTCATTCTGTTACCTAGTCTGGAGTGCACTGGTGTGATCTCAGCTCACCGTAGCCTCACCCTC A G BRCA2 Ensembl:ENSG00000139618 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1325160145 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109405,RMVar_hsa_circ_120972,RMVar_hsa_circ_362683,RMVar_hsa_circ_162618,RMVar_hsa_circ_61551,RMVar_hsa_circ_162622 34811 RMVar_ID_34811 Human_SNP_ID_525992611 A-to-I Human chr13 + 32336061 32336061 32336061 ACACCACCACACCCAGCTAATTTTTATTTTTCATAGAGTCATGGTCTCACTATGTTGCCCAGGCT ACACCACCACACCCAGCTAATTTTTATTTTTCGTAGAGTCATGGTCTCACTATGTTGCCCAGGCT A G BRCA2 Ensembl:ENSG00000139618 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1339430846 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109405,RMVar_hsa_circ_120972,RMVar_hsa_circ_362683,RMVar_hsa_circ_162618,RMVar_hsa_circ_61551,RMVar_hsa_circ_162622 34812 RMVar_ID_34812 Human_SNP_ID_526014348 A-to-I Human chr13 + 32399062 32399062 32399062 GTGGCTCATGCCTGTAATCCCAACACTTTGAGAAGCTGAGGTGGGAGGAGTGCTTGAGGCCAGGA GTGGCTCATGCCTGTAATCCCAACACTTTGAGCAGCTGAGGTGGGAGGAGTGCTTGAGGCCAGGA A C BRCA2 Ensembl:ENSG00000139618 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs886050112 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_108 RMVar_hsa_circ_120972,RMVar_hsa_circ_162618 34813 RMVar_ID_34813 Human_SNP_ID_526014573 A-to-I Human chr13 + 32399966 32399966 32399966 CACCACCATGCCCAGCTAATTTTTGCATTTTTAGTAGAGACTGGGTTTTACCATGTTGGCCAAGC CACCACCATGCCCAGCTAATTTTTGCATTTTTGGTAGAGACTGGGTTTTACCATGTTGGCCAAGC A G BRCA2 Ensembl:ENSG00000139618 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474662928 Functional Loss SNV dbSNP153 33..33 33 - - - 34814 RMVar_ID_34814 Human_SNP_ID_526014577 A-to-I Human chr13 + 32399995 32399995 32399995 TTTAGTAGAGACTGGGTTTTACCATGTTGGCCAAGCTGGTCTCAAACTCCTGATGTCAGGTGATC TTTAGTAGAGACTGGGTTTTACCATGTTGGCCGAGCTGGTCTCAAACTCCTGATGTCAGGTGATC A G BRCA2 Ensembl:ENSG00000139618 Protein coding 3'UTR GSE100210;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229 RNA-Seq:(High) rs1426227797 Functional Loss SNV dbSNP153 33..33 33 - - - 34815 RMVar_ID_34815 Human_SNP_ID_526017551 A-to-I Human chr13 - 32412435 32412435 32412435 TTTAGTAGAGACGGGATTTTGCCGTGTTGGCCAGGCTGGTCTCAAACTCCTGACCTCAAGTGATC TTTAGTAGAGACGGGATTTTGCCGTGTTGGCCGGGCTGGTCTCAAACTCCTGACCTCAAGTGATC T C N4BP2L1 Ensembl:ENSG00000139597 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1051091409 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64916 34816 RMVar_ID_34816 Human_SNP_ID_526023348 A-to-I Human chr13 - 32436730 32436730 32436730 GCTGGAGTGCAGTGGCGTGATCTCAGCTCGCTACAACTTCTGACTCCCAGGTTCAGGTGATTCTC GCTGGAGTGCAGTGGCGTGATCTCAGCTCGCTGCAACTTCTGACTCCCAGGTTCAGGTGATTCTC T C N4BP2L2 Ensembl:ENSG00000244754 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350506722 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_162628,RMVar_hsa_circ_162630,RMVar_hsa_circ_162632,RMVar_hsa_circ_162631,RMVar_hsa_circ_162629,RMVar_hsa_circ_162633,RMVar_hsa_circ_35673,RMVar_hsa_circ_340105,RMVar_hsa_circ_162627,RMVar_hsa_circ_356773,RMVar_hsa_circ_316102,RMVar_hsa_circ_11247 34817 RMVar_ID_34817 Human_SNP_ID_526030767 A-to-I Human chr13 - 32467988 32467988 32467988 AAATGCATTATTTTCCTTTTTCTATTTTTTTGAGACAGAGTCTTGCTCTGTTGCCTATGCAACAG AAATGCATTATTTTCCTTTTTCTATTTTTTTGTGACAGAGTCTTGCTCTGTTGCCTATGCAACAG T A N4BP2L2 Ensembl:ENSG00000244754 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1011008952 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16530,RMVar_hsa_circ_162628,RMVar_hsa_circ_162630,RMVar_hsa_circ_162631,RMVar_hsa_circ_162629,RMVar_hsa_circ_35673,RMVar_hsa_circ_340105,RMVar_hsa_circ_162627,RMVar_hsa_circ_11247,RMVar_hsa_circ_267269,RMVar_hsa_circ_331234,RMVar_hsa_circ_357782,RMVar_hsa_circ_57407,RMVar_hsa_circ_16407,RMVar_hsa_circ_339451,RMVar_hsa_circ_326544,RMVar_hsa_circ_68852,RMVar_hsa_circ_162636 34818 RMVar_ID_34818 Human_SNP_ID_526034442 A-to-I Human chr13 - 32484251 32484251 32484251 ATGATCTCGGCTCGCTGCAGCCTTGACCTCCTAGGCTGAAGCAATCCTCCCACCTCAGTTCACCC ATGATCTCGGCTCGCTGCAGCCTTGACCTCCTGGGCTGAAGCAATCCTCCCACCTCAGTTCACCC T C N4BP2L2 Ensembl:ENSG00000244754 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs931512741 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16530,RMVar_hsa_circ_162628,RMVar_hsa_circ_162630,RMVar_hsa_circ_162629,RMVar_hsa_circ_35673,RMVar_hsa_circ_340105,RMVar_hsa_circ_162627,RMVar_hsa_circ_267269,RMVar_hsa_circ_331234,RMVar_hsa_circ_57407,RMVar_hsa_circ_162640,RMVar_hsa_circ_16407,RMVar_hsa_circ_339451,RMVar_hsa_circ_68852,RMVar_hsa_circ_162636,RMVar_hsa_circ_101362,RMVar_hsa_circ_162638,RMVar_hsa_circ_162639,RMVar_hsa_circ_162641,RMVar_hsa_circ_162642 34819 RMVar_ID_34819 Human_SNP_ID_526034518 A-to-I Human chr13 - 32484612 32484612 32484612 GGCGTGGTGGCGCTGTGCCAGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGGATCCTTTGAA GGCGTGGTGGCGCTGTGCCAGTAATCCCAGCTGCTTGGGAGGCTGAGGCAGGAGGATCCTTTGAA T C N4BP2L2 Ensembl:ENSG00000244754 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1216400397 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16530,RMVar_hsa_circ_162628,RMVar_hsa_circ_162630,RMVar_hsa_circ_162629,RMVar_hsa_circ_35673,RMVar_hsa_circ_340105,RMVar_hsa_circ_162627,RMVar_hsa_circ_267269,RMVar_hsa_circ_331234,RMVar_hsa_circ_57407,RMVar_hsa_circ_162640,RMVar_hsa_circ_16407,RMVar_hsa_circ_339451,RMVar_hsa_circ_68852,RMVar_hsa_circ_162636,RMVar_hsa_circ_101362,RMVar_hsa_circ_162638,RMVar_hsa_circ_162639,RMVar_hsa_circ_162641,RMVar_hsa_circ_162642 34820 RMVar_ID_34820 Human_SNP_ID_526034522 A-to-I Human chr13 - 32484621 32484621 32484621 AATTAGCTGGGCGTGGTGGCGCTGTGCCAGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGGA AATTAGCTGGGCGTGGTGGCGCTGTGCCAGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGGA T C N4BP2L2 Ensembl:ENSG00000244754 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1219736372 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16530,RMVar_hsa_circ_162628,RMVar_hsa_circ_162630,RMVar_hsa_circ_162629,RMVar_hsa_circ_35673,RMVar_hsa_circ_340105,RMVar_hsa_circ_162627,RMVar_hsa_circ_267269,RMVar_hsa_circ_331234,RMVar_hsa_circ_57407,RMVar_hsa_circ_162640,RMVar_hsa_circ_16407,RMVar_hsa_circ_339451,RMVar_hsa_circ_68852,RMVar_hsa_circ_162636,RMVar_hsa_circ_101362,RMVar_hsa_circ_162638,RMVar_hsa_circ_162639,RMVar_hsa_circ_162641,RMVar_hsa_circ_162642 34821 RMVar_ID_34821 Human_SNP_ID_526035815 A-to-I Human chr13 - 32490508 32490508 32490508 CTAAGGTCAGGAGTTGAAGACAAGCCTGGTCAACATAGTGAGACCTAGTCTCTACTAAAAATACA CTAAGGTCAGGAGTTGAAGACAAGCCTGGTCACCATAGTGAGACCTAGTCTCTACTAAAAATACA T G N4BP2L2 Ensembl:ENSG00000244754 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1410192436 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16530,RMVar_hsa_circ_162628,RMVar_hsa_circ_162630,RMVar_hsa_circ_162629,RMVar_hsa_circ_35673,RMVar_hsa_circ_340105,RMVar_hsa_circ_162627,RMVar_hsa_circ_267269,RMVar_hsa_circ_331234,RMVar_hsa_circ_57407,RMVar_hsa_circ_162640,RMVar_hsa_circ_16407,RMVar_hsa_circ_339451,RMVar_hsa_circ_68852,RMVar_hsa_circ_162636,RMVar_hsa_circ_101362,RMVar_hsa_circ_162638,RMVar_hsa_circ_162639,RMVar_hsa_circ_162641,RMVar_hsa_circ_162642 34822 RMVar_ID_34822 Human_SNP_ID_526037286 A-to-I Human chr13 - 32495835 32495835 32495835 TACTGAAAATACAAAAATTACCTGGGCATGGTAGCAGACACCTGTAATCCCAGCTACTCAGGAGA TACTGAAAATACAAAAATTACCTGGGCATGGTGGCAGACACCTGTAATCCCAGCTACTCAGGAGA T C N4BP2L2 Ensembl:ENSG00000244754 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1472412834 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16530,RMVar_hsa_circ_162628,RMVar_hsa_circ_162630,RMVar_hsa_circ_162629,RMVar_hsa_circ_35673,RMVar_hsa_circ_340105,RMVar_hsa_circ_162627,RMVar_hsa_circ_267269,RMVar_hsa_circ_331234,RMVar_hsa_circ_57407,RMVar_hsa_circ_162640,RMVar_hsa_circ_16407,RMVar_hsa_circ_339451,RMVar_hsa_circ_68852,RMVar_hsa_circ_162636,RMVar_hsa_circ_101362,RMVar_hsa_circ_162638,RMVar_hsa_circ_162639,RMVar_hsa_circ_162641,RMVar_hsa_circ_162642 34823 RMVar_ID_34823 Human_SNP_ID_526037820 A-to-I Human chr13 - 32498125 32498125 32498125 TAAAAATTAGCCAAGTATGGTGGCATATGCCTATATTCTAGCTACTCAGGAGGCTGAGATGGGAG TAAAAATTAGCCAAGTATGGTGGCATATGCCTGTATTCTAGCTACTCAGGAGGCTGAGATGGGAG T C N4BP2L2 Ensembl:ENSG00000244754 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs748245690 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12133758 RMVar_hsa_circ_16530,RMVar_hsa_circ_162628,RMVar_hsa_circ_162630,RMVar_hsa_circ_162629,RMVar_hsa_circ_35673,RMVar_hsa_circ_340105,RMVar_hsa_circ_162627,RMVar_hsa_circ_267269,RMVar_hsa_circ_331234,RMVar_hsa_circ_57407,RMVar_hsa_circ_162640,RMVar_hsa_circ_16407,RMVar_hsa_circ_339451,RMVar_hsa_circ_68852,RMVar_hsa_circ_162636,RMVar_hsa_circ_101362,RMVar_hsa_circ_162638,RMVar_hsa_circ_162639,RMVar_hsa_circ_162641,RMVar_hsa_circ_162642 34824 RMVar_ID_34824 Human_SNP_ID_526038552 A-to-I Human chr13 - 32501050 32501050 32501050 CAGCCTGGGTAAAATGGCGAAACCTCGTCTTTACTAAAAATACAAAATTAGCTGGGCGTCGTGAT CAGCCTGGGTAAAATGGCGAAACCTCGTCTTTCCTAAAAATACAAAATTAGCTGGGCGTCGTGAT T G N4BP2L2 Ensembl:ENSG00000244754 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037143372 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16530,RMVar_hsa_circ_162628,RMVar_hsa_circ_162630,RMVar_hsa_circ_162629,RMVar_hsa_circ_35673,RMVar_hsa_circ_340105,RMVar_hsa_circ_162627,RMVar_hsa_circ_267269,RMVar_hsa_circ_331234,RMVar_hsa_circ_57407,RMVar_hsa_circ_162640,RMVar_hsa_circ_16407,RMVar_hsa_circ_339451,RMVar_hsa_circ_68852,RMVar_hsa_circ_162636,RMVar_hsa_circ_101362,RMVar_hsa_circ_162638,RMVar_hsa_circ_162639,RMVar_hsa_circ_162641,RMVar_hsa_circ_162642 34825 RMVar_ID_34825 Human_SNP_ID_526038867 A-to-I Human chr13 - 32502181 32502181 32502181 TGCATGCCTGTAATCCCAGCTACTTGAAGGCTAAGGTAGGAGAATTCCTTGAACCCAGGAGGGCA TGCATGCCTGTAATCCCAGCTACTTGAAGGCTGAGGTAGGAGAATTCCTTGAACCCAGGAGGGCA T C N4BP2L2 Ensembl:ENSG00000244754 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1311307157 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16530,RMVar_hsa_circ_162628,RMVar_hsa_circ_162630,RMVar_hsa_circ_162629,RMVar_hsa_circ_35673,RMVar_hsa_circ_340105,RMVar_hsa_circ_162627,RMVar_hsa_circ_267269,RMVar_hsa_circ_331234,RMVar_hsa_circ_57407,RMVar_hsa_circ_162640,RMVar_hsa_circ_16407,RMVar_hsa_circ_339451,RMVar_hsa_circ_68852,RMVar_hsa_circ_162636,RMVar_hsa_circ_101362,RMVar_hsa_circ_162638,RMVar_hsa_circ_162639,RMVar_hsa_circ_162641,RMVar_hsa_circ_162642 34826 RMVar_ID_34826 Human_SNP_ID_526038910 A-to-I Human chr13 - 32502356 32502354 32502356 TAGTTAGCAATGCTGTAATAGGCTGGGCTCACACCTGTAATCCCAGCACTTTGGGAGGTTGAGGA TAGTTAGCAATGCTGTAATAGGCTGGGCTCAC__CTGTAATCCCAGCACTTTGGGAGGTTGAGGA GGT G N4BP2L2 Ensembl:ENSG00000244754 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1463209624 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_16530,RMVar_hsa_circ_162628,RMVar_hsa_circ_162630,RMVar_hsa_circ_162629,RMVar_hsa_circ_35673,RMVar_hsa_circ_340105,RMVar_hsa_circ_162627,RMVar_hsa_circ_267269,RMVar_hsa_circ_331234,RMVar_hsa_circ_57407,RMVar_hsa_circ_162640,RMVar_hsa_circ_16407,RMVar_hsa_circ_339451,RMVar_hsa_circ_68852,RMVar_hsa_circ_162636,RMVar_hsa_circ_101362,RMVar_hsa_circ_162638,RMVar_hsa_circ_162639,RMVar_hsa_circ_162641,RMVar_hsa_circ_162642 34827 RMVar_ID_34827 Human_SNP_ID_526039068 A-to-I Human chr13 - 32503051 32503051 32503051 CTCCTGCCTCAGCCTCCCGAGTCGCTGGGATTACAGGTGCCTACCACCACGCCCGACTAATTTTT CTCCTGCCTCAGCCTCCCGAGTCGCTGGGATTGCAGGTGCCTACCACCACGCCCGACTAATTTTT T C N4BP2L2 Ensembl:ENSG00000244754 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1373029399 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16530,RMVar_hsa_circ_162628,RMVar_hsa_circ_162630,RMVar_hsa_circ_162629,RMVar_hsa_circ_35673,RMVar_hsa_circ_340105,RMVar_hsa_circ_162627,RMVar_hsa_circ_267269,RMVar_hsa_circ_331234,RMVar_hsa_circ_57407,RMVar_hsa_circ_162640,RMVar_hsa_circ_16407,RMVar_hsa_circ_339451,RMVar_hsa_circ_68852,RMVar_hsa_circ_162636,RMVar_hsa_circ_101362,RMVar_hsa_circ_162638,RMVar_hsa_circ_162639,RMVar_hsa_circ_162641,RMVar_hsa_circ_162642 34828 RMVar_ID_34828 Human_SNP_ID_526039098 A-to-I Human chr13 - 32503151 32503151 32503151 TTTTTTTTTTTGCTACAGAGTCTTGCTCTGTCACCTAGGCTGTACTGCAGTGGCATGATCTCAGC TTTTTTTTTTTGCTACAGAGTCTTGCTCTGTCTCCTAGGCTGTACTGCAGTGGCATGATCTCAGC T A N4BP2L2 Ensembl:ENSG00000244754 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs993947942 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6271718,Human_RBP_ID_12133955,Human_RBP_ID_23591827 Human_miRNA_ID_2877617 RMVar_hsa_circ_16530,RMVar_hsa_circ_162628,RMVar_hsa_circ_162630,RMVar_hsa_circ_162629,RMVar_hsa_circ_35673,RMVar_hsa_circ_340105,RMVar_hsa_circ_162627,RMVar_hsa_circ_267269,RMVar_hsa_circ_331234,RMVar_hsa_circ_57407,RMVar_hsa_circ_162640,RMVar_hsa_circ_16407,RMVar_hsa_circ_339451,RMVar_hsa_circ_68852,RMVar_hsa_circ_162636,RMVar_hsa_circ_101362,RMVar_hsa_circ_162638,RMVar_hsa_circ_162639,RMVar_hsa_circ_162641,RMVar_hsa_circ_162642 34829 RMVar_ID_34829 Human_SNP_ID_526039301 A-to-I Human chr13 - 32503965 32503965 32503965 GAGTCTTTTTCTTTCACCCAGGCTGCCAGGCTAGAGTGCAGTGGCGCAATCATAGTTCACTGTAA GAGTCTTTTTCTTTCACCCAGGCTGCCAGGCTGGAGTGCAGTGGCGCAATCATAGTTCACTGTAA T C N4BP2L2 Ensembl:ENSG00000244754 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1345510306 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12133989,Human_RBP_ID_17836156 RMVar_hsa_circ_16530,RMVar_hsa_circ_162628,RMVar_hsa_circ_162630,RMVar_hsa_circ_162629,RMVar_hsa_circ_35673,RMVar_hsa_circ_340105,RMVar_hsa_circ_162627,RMVar_hsa_circ_267269,RMVar_hsa_circ_331234,RMVar_hsa_circ_57407,RMVar_hsa_circ_162640,RMVar_hsa_circ_16407,RMVar_hsa_circ_339451,RMVar_hsa_circ_68852,RMVar_hsa_circ_162636,RMVar_hsa_circ_101362,RMVar_hsa_circ_162638,RMVar_hsa_circ_162639,RMVar_hsa_circ_162641,RMVar_hsa_circ_162642 34830 RMVar_ID_34830 Human_SNP_ID_526040988 A-to-I Human chr13 - 32510702 32510702 32510702 CTGAGGTGAGGCGTTGGAGACCAGCCTGGCCAACGTGGTGAAACCCTGTCTTTACTAAAGATACA CTGAGGTGAGGCGTTGGAGACCAGCCTGGCCAGCGTGGTGAAACCCTGTCTTTACTAAAGATACA T C N4BP2L2 Ensembl:ENSG00000244754 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1159055335 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24366543 RMVar_hsa_circ_16530,RMVar_hsa_circ_162628,RMVar_hsa_circ_162630,RMVar_hsa_circ_162629,RMVar_hsa_circ_35673,RMVar_hsa_circ_340105,RMVar_hsa_circ_162627,RMVar_hsa_circ_267269,RMVar_hsa_circ_331234,RMVar_hsa_circ_57407,RMVar_hsa_circ_162640,RMVar_hsa_circ_16407,RMVar_hsa_circ_339451,RMVar_hsa_circ_68852,RMVar_hsa_circ_162636,RMVar_hsa_circ_101362,RMVar_hsa_circ_162638,RMVar_hsa_circ_162639,RMVar_hsa_circ_162641,RMVar_hsa_circ_162642 34831 RMVar_ID_34831 Human_SNP_ID_526041868 A-to-I Human chr13 - 32514632 32514632 32514632 CAGTCTTTTTTGGGGGTTGGGGTTAAGAGATGAGGTCTCTTTCTGTTGTATAGACTGGACTTGAA CAGTCTTTTTTGGGGGTTGGGGTTAAGAGATGCGGTCTCTTTCTGTTGTATAGACTGGACTTGAA T G N4BP2L2 Ensembl:ENSG00000244754 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs575737813 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_756175,Human_RBP_ID_6271904,Human_RBP_ID_9030153,Human_RBP_ID_12134510 RMVar_hsa_circ_16530,RMVar_hsa_circ_162628,RMVar_hsa_circ_162630,RMVar_hsa_circ_162629,RMVar_hsa_circ_35673,RMVar_hsa_circ_340105,RMVar_hsa_circ_162627,RMVar_hsa_circ_267269,RMVar_hsa_circ_331234,RMVar_hsa_circ_57407,RMVar_hsa_circ_162640,RMVar_hsa_circ_16407,RMVar_hsa_circ_339451,RMVar_hsa_circ_68852,RMVar_hsa_circ_162636,RMVar_hsa_circ_101362,RMVar_hsa_circ_162638,RMVar_hsa_circ_162639,RMVar_hsa_circ_162641,RMVar_hsa_circ_162642 34832 RMVar_ID_34832 Human_SNP_ID_526042156 A-to-I Human chr13 - 32515811 32515811 32515811 ATCGCTTGAACCTGGGAGGCAGAGTTTGCAGTAAGCAGAGATTGCGCCACTTGCACTCCAGCCTG ATCGCTTGAACCTGGGAGGCAGAGTTTGCAGTGAGCAGAGATTGCGCCACTTGCACTCCAGCCTG T C N4BP2L2 Ensembl:ENSG00000244754 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1038725550 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25042298 RMVar_hsa_circ_16530,RMVar_hsa_circ_162628,RMVar_hsa_circ_162630,RMVar_hsa_circ_162629,RMVar_hsa_circ_35673,RMVar_hsa_circ_340105,RMVar_hsa_circ_162627,RMVar_hsa_circ_267269,RMVar_hsa_circ_331234,RMVar_hsa_circ_57407,RMVar_hsa_circ_162640,RMVar_hsa_circ_16407,RMVar_hsa_circ_339451,RMVar_hsa_circ_68852,RMVar_hsa_circ_162636,RMVar_hsa_circ_101362,RMVar_hsa_circ_162638,RMVar_hsa_circ_162639,RMVar_hsa_circ_162641,RMVar_hsa_circ_162642 34833 RMVar_ID_34833 Human_SNP_ID_526042186 A-to-I Human chr13 - 32515913 32515913 32515913 TCTGACACAGTGAAACCACATCTCTACTTAAAATACAAAAATCAGCTGGGTGTGGTGGTGTGTGC TCTGACACAGTGAAACCACATCTCTACTTAAACTACAAAAATCAGCTGGGTGTGGTGGTGTGTGC T G N4BP2L2 Ensembl:ENSG00000244754 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1183087050 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16530,RMVar_hsa_circ_162628,RMVar_hsa_circ_162630,RMVar_hsa_circ_162629,RMVar_hsa_circ_35673,RMVar_hsa_circ_340105,RMVar_hsa_circ_162627,RMVar_hsa_circ_267269,RMVar_hsa_circ_331234,RMVar_hsa_circ_57407,RMVar_hsa_circ_162640,RMVar_hsa_circ_16407,RMVar_hsa_circ_339451,RMVar_hsa_circ_68852,RMVar_hsa_circ_162636,RMVar_hsa_circ_101362,RMVar_hsa_circ_162638,RMVar_hsa_circ_162639,RMVar_hsa_circ_162641,RMVar_hsa_circ_162642 34834 RMVar_ID_34834 Human_SNP_ID_526044418 A-to-I Human chr13 - 32524846 32524846 32524846 AGATAGGAGGATTGCTTGAGGCAGGGAGGTCAAGGCTGCAGTGAGCTGAGATCATGCTACTGCAC AGATAGGAGGATTGCTTGAGGCAGGGAGGTCAGGGCTGCAGTGAGCTGAGATCATGCTACTGCAC T C N4BP2L2 Ensembl:ENSG00000244754 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs541227023 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12134988 RMVar_hsa_circ_16530,RMVar_hsa_circ_35673,RMVar_hsa_circ_162627,RMVar_hsa_circ_68852,RMVar_hsa_circ_101362,RMVar_hsa_circ_162639,RMVar_hsa_circ_162642,RMVar_hsa_circ_162645,RMVar_hsa_circ_279929,RMVar_hsa_circ_266394,RMVar_hsa_circ_374349,RMVar_hsa_circ_275780,RMVar_hsa_circ_162643,RMVar_hsa_circ_162644,RMVar_hsa_circ_162649,RMVar_hsa_circ_97693,RMVar_hsa_circ_286002,RMVar_hsa_circ_162648,RMVar_hsa_circ_311792 34835 RMVar_ID_34835 Human_SNP_ID_526044447 A-to-I Human chr13 - 32524945 32524945 32524945 CAGCCTGGGCAACATGATGAAACCCCATCTCTACAAAAAGTAGAAAAATTAGCCAGGTGTGGTGG CAGCCTGGGCAACATGATGAAACCCCATCTCTTCAAAAAGTAGAAAAATTAGCCAGGTGTGGTGG T A N4BP2L2 Ensembl:ENSG00000244754 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1010496129 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_118414,Human_RBP_ID_25042513 RMVar_hsa_circ_16530,RMVar_hsa_circ_35673,RMVar_hsa_circ_162627,RMVar_hsa_circ_68852,RMVar_hsa_circ_101362,RMVar_hsa_circ_162639,RMVar_hsa_circ_162642,RMVar_hsa_circ_162645,RMVar_hsa_circ_279929,RMVar_hsa_circ_266394,RMVar_hsa_circ_374349,RMVar_hsa_circ_275780,RMVar_hsa_circ_162643,RMVar_hsa_circ_162644,RMVar_hsa_circ_162649,RMVar_hsa_circ_97693,RMVar_hsa_circ_286002,RMVar_hsa_circ_162648,RMVar_hsa_circ_311792 34836 RMVar_ID_34836 Human_SNP_ID_526044467 A-to-I Human chr13 - 32525013 32525013 32525013 CATGCCTATAATCCCAGCACTTTGGGAGGCCGAGGCGGGCAGATCACTTGAGCCCAGGAGTTAGA CATGCCTATAATCCCAGCACTTTGGGAGGCCGCGGCGGGCAGATCACTTGAGCCCAGGAGTTAGA T G N4BP2L2 Ensembl:ENSG00000244754 Protein coding intron GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1297918776 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_118414 RMVar_hsa_circ_16530,RMVar_hsa_circ_35673,RMVar_hsa_circ_162627,RMVar_hsa_circ_68852,RMVar_hsa_circ_101362,RMVar_hsa_circ_162639,RMVar_hsa_circ_162642,RMVar_hsa_circ_162645,RMVar_hsa_circ_279929,RMVar_hsa_circ_266394,RMVar_hsa_circ_374349,RMVar_hsa_circ_275780,RMVar_hsa_circ_162643,RMVar_hsa_circ_162644,RMVar_hsa_circ_162649,RMVar_hsa_circ_97693,RMVar_hsa_circ_286002,RMVar_hsa_circ_162648,RMVar_hsa_circ_311792 34837 RMVar_ID_34837 Human_SNP_ID_526044603 A-to-I Human chr13 - 32525569 32525569 32525569 GAATTCCTGGACTCAAGGGATCCTCCTGCCTCAGCCTCCTGAGTAACTAGGACTACAGGCAGGTA GAATTCCTGGACTCAAGGGATCCTCCTGCCTCGGCCTCCTGAGTAACTAGGACTACAGGCAGGTA T C N4BP2L2 Ensembl:ENSG00000244754 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1134473 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16530,RMVar_hsa_circ_35673,RMVar_hsa_circ_162627,RMVar_hsa_circ_68852,RMVar_hsa_circ_101362,RMVar_hsa_circ_162639,RMVar_hsa_circ_162642,RMVar_hsa_circ_162645,RMVar_hsa_circ_279929,RMVar_hsa_circ_266394,RMVar_hsa_circ_374349,RMVar_hsa_circ_275780,RMVar_hsa_circ_162643,RMVar_hsa_circ_162644,RMVar_hsa_circ_162649,RMVar_hsa_circ_97693,RMVar_hsa_circ_286002,RMVar_hsa_circ_162648,RMVar_hsa_circ_311792 34838 RMVar_ID_34838 Human_SNP_ID_526044609 A-to-I Human chr13 - 32525612 32525612 32525612 CAGGCTAGAGCGTAGTGACACAATCATAGCTCAGTGCAGCCTCGAATTCCTGGACTCAAGGGATC CAGGCTAGAGCGTAGTGACACAATCATAGCTCCGTGCAGCCTCGAATTCCTGGACTCAAGGGATC T G N4BP2L2 Ensembl:ENSG00000244754 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560847842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230521,Human_RBP_ID_12135039 RMVar_hsa_circ_16530,RMVar_hsa_circ_35673,RMVar_hsa_circ_162627,RMVar_hsa_circ_68852,RMVar_hsa_circ_101362,RMVar_hsa_circ_162639,RMVar_hsa_circ_162642,RMVar_hsa_circ_162645,RMVar_hsa_circ_279929,RMVar_hsa_circ_266394,RMVar_hsa_circ_374349,RMVar_hsa_circ_275780,RMVar_hsa_circ_162643,RMVar_hsa_circ_162644,RMVar_hsa_circ_162649,RMVar_hsa_circ_97693,RMVar_hsa_circ_286002,RMVar_hsa_circ_162648,RMVar_hsa_circ_311792 34839 RMVar_ID_34839 Human_SNP_ID_526044620 A-to-I Human chr13 - 32525667 32525667 32525667 AATTTCAGTGAGGATGTTTGTGTGTGTTTTAGAGATGGGGTCTTGCTTTGTTGCCCAGGCTAGAG AATTTCAGTGAGGATGTTTGTGTGTGTTTTAGGGATGGGGTCTTGCTTTGTTGCCCAGGCTAGAG T C N4BP2L2 Ensembl:ENSG00000244754 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1134475 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6272119,Human_RBP_ID_9724998,Human_RBP_ID_12135041,Human_RBP_ID_23591996 RMVar_hsa_circ_16530,RMVar_hsa_circ_35673,RMVar_hsa_circ_162627,RMVar_hsa_circ_68852,RMVar_hsa_circ_101362,RMVar_hsa_circ_162639,RMVar_hsa_circ_162642,RMVar_hsa_circ_162645,RMVar_hsa_circ_279929,RMVar_hsa_circ_266394,RMVar_hsa_circ_374349,RMVar_hsa_circ_275780,RMVar_hsa_circ_162643,RMVar_hsa_circ_162644,RMVar_hsa_circ_162649,RMVar_hsa_circ_97693,RMVar_hsa_circ_286002,RMVar_hsa_circ_162648,RMVar_hsa_circ_311792 34840 RMVar_ID_34840 Human_SNP_ID_526044621 A-to-I Human chr13 - 32525669 32525669 32525669 GGAATTTCAGTGAGGATGTTTGTGTGTGTTTTAGAGATGGGGTCTTGCTTTGTTGCCCAGGCTAG GGAATTTCAGTGAGGATGTTTGTGTGTGTTTTGGAGATGGGGTCTTGCTTTGTTGCCCAGGCTAG T C N4BP2L2 Ensembl:ENSG00000244754 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs3168729 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6272119,Human_RBP_ID_9724998,Human_RBP_ID_12135041,Human_RBP_ID_23591996 RMVar_hsa_circ_16530,RMVar_hsa_circ_35673,RMVar_hsa_circ_162627,RMVar_hsa_circ_68852,RMVar_hsa_circ_101362,RMVar_hsa_circ_162639,RMVar_hsa_circ_162642,RMVar_hsa_circ_162645,RMVar_hsa_circ_279929,RMVar_hsa_circ_266394,RMVar_hsa_circ_374349,RMVar_hsa_circ_275780,RMVar_hsa_circ_162643,RMVar_hsa_circ_162644,RMVar_hsa_circ_162649,RMVar_hsa_circ_97693,RMVar_hsa_circ_286002,RMVar_hsa_circ_162648,RMVar_hsa_circ_311792 34841 RMVar_ID_34841 Human_SNP_ID_526081369 A-to-I Human chr13 + 32665798 32665798 32665798 ATCAATGGATGAGTGTATAAAGAAATTGTGGTATATGTATACAATGGAATATTATTCCAGCCATA ATCAATGGATGAGTGTATAAAGAAATTGTGGTGTATGTATACAATGGAATATTATTCCAGCCATA A G PDS5B Ensembl:ENSG00000083642 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs948678529 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_506,RMVar_hsa_circ_32585,RMVar_hsa_circ_162656,RMVar_hsa_circ_304042,RMVar_hsa_circ_334771,RMVar_hsa_circ_354316,RMVar_hsa_circ_375788,RMVar_hsa_circ_162655,RMVar_hsa_circ_357558,RMVar_hsa_circ_340371,RMVar_hsa_circ_307948,RMVar_hsa_circ_323421,RMVar_hsa_circ_299159,RMVar_hsa_circ_274851,RMVar_hsa_circ_42659,RMVar_hsa_circ_162660,RMVar_hsa_circ_162662,RMVar_hsa_circ_162663,RMVar_hsa_circ_162661,RMVar_hsa_circ_162659,RMVar_hsa_circ_336933,RMVar_hsa_circ_369687,RMVar_hsa_circ_319512,RMVar_hsa_circ_269503,RMVar_hsa_circ_272031,RMVar_hsa_circ_47325,RMVar_hsa_circ_83008,RMVar_hsa_circ_162667,RMVar_hsa_circ_12629,RMVar_hsa_circ_26125,RMVar_hsa_circ_162668,RMVar_hsa_circ_162665,RMVar_hsa_circ_162666,RMVar_hsa_circ_162664,RMVar_hsa_circ_14831,RMVar_hsa_circ_35950,RMVar_hsa_circ_162670,RMVar_hsa_circ_11142 34842 RMVar_ID_34842 Human_SNP_ID_526085929 A-to-I Human chr13 + 32684000 32684000 32684000 TTCTGGTCAATGATCACTTACTTAATTTTGTGAGAGAGAGAACATTAGACAAACGAGTAAGTATG TTCTGGTCAATGATCACTTACTTAATTTTGTGTGAGAGAGAACATTAGACAAACGAGTAAGTATG A T PDS5B Ensembl:ENSG00000083642 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs750827034 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12137303 Human_Splice_Rec_1455459,Human_Splice_Rec_1455529,Human_Splice_Rec_1455551 RMVar_hsa_circ_506,RMVar_hsa_circ_32585,RMVar_hsa_circ_162656,RMVar_hsa_circ_334771,RMVar_hsa_circ_354316,RMVar_hsa_circ_375788,RMVar_hsa_circ_162655,RMVar_hsa_circ_340371,RMVar_hsa_circ_307948,RMVar_hsa_circ_323421,RMVar_hsa_circ_274851,RMVar_hsa_circ_42659,RMVar_hsa_circ_162662,RMVar_hsa_circ_162663,RMVar_hsa_circ_162661,RMVar_hsa_circ_336933,RMVar_hsa_circ_319512,RMVar_hsa_circ_47325,RMVar_hsa_circ_83008,RMVar_hsa_circ_12629,RMVar_hsa_circ_26125,RMVar_hsa_circ_162665,RMVar_hsa_circ_162666,RMVar_hsa_circ_162664,RMVar_hsa_circ_162670,RMVar_hsa_circ_11142,RMVar_hsa_circ_1730,RMVar_hsa_circ_11295,RMVar_hsa_circ_13352,RMVar_hsa_circ_16800,RMVar_hsa_circ_6430,RMVar_hsa_circ_312531,RMVar_hsa_circ_348095,RMVar_hsa_circ_366649,RMVar_hsa_circ_345176,RMVar_hsa_circ_41627,RMVar_hsa_circ_66982,RMVar_hsa_circ_38471,RMVar_hsa_circ_62706,RMVar_hsa_circ_162673,RMVar_hsa_circ_162674,RMVar_hsa_circ_126623,RMVar_hsa_circ_162676,RMVar_hsa_circ_38159,RMVar_hsa_circ_162675,RMVar_hsa_circ_311093,RMVar_hsa_circ_336662,RMVar_hsa_circ_162677,RMVar_hsa_circ_41772,RMVar_hsa_circ_313993,RMVar_hsa_circ_316841,RMVar_hsa_circ_44434,RMVar_hsa_circ_37225,RMVar_hsa_circ_162678 34843 RMVar_ID_34843 Human_SNP_ID_526086334 A-to-I Human chr13 + 32685743 32685743 32685743 TCACGGCTCATTGCATCCTTGACCTGGGTTCCAACAGTCCTCCCACCTCAGCCTCCTGAGTAGGT TCACGGCTCATTGCATCCTTGACCTGGGTTCCCACAGTCCTCCCACCTCAGCCTCCTGAGTAGGT A C PDS5B Ensembl:ENSG00000083642 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs945281783 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32585,RMVar_hsa_circ_162656,RMVar_hsa_circ_334771,RMVar_hsa_circ_354316,RMVar_hsa_circ_375788,RMVar_hsa_circ_162655,RMVar_hsa_circ_307948,RMVar_hsa_circ_323421,RMVar_hsa_circ_274851,RMVar_hsa_circ_42659,RMVar_hsa_circ_162662,RMVar_hsa_circ_162663,RMVar_hsa_circ_162661,RMVar_hsa_circ_319512,RMVar_hsa_circ_47325,RMVar_hsa_circ_83008,RMVar_hsa_circ_12629,RMVar_hsa_circ_26125,RMVar_hsa_circ_162665,RMVar_hsa_circ_162664,RMVar_hsa_circ_162670,RMVar_hsa_circ_11142,RMVar_hsa_circ_1730,RMVar_hsa_circ_11295,RMVar_hsa_circ_13352,RMVar_hsa_circ_16800,RMVar_hsa_circ_6430,RMVar_hsa_circ_312531,RMVar_hsa_circ_348095,RMVar_hsa_circ_366649,RMVar_hsa_circ_345176,RMVar_hsa_circ_41627,RMVar_hsa_circ_38471,RMVar_hsa_circ_62706,RMVar_hsa_circ_162673,RMVar_hsa_circ_162674,RMVar_hsa_circ_126623,RMVar_hsa_circ_162676,RMVar_hsa_circ_38159,RMVar_hsa_circ_162675,RMVar_hsa_circ_311093,RMVar_hsa_circ_336662,RMVar_hsa_circ_162677,RMVar_hsa_circ_41772,RMVar_hsa_circ_313993,RMVar_hsa_circ_316841,RMVar_hsa_circ_44434,RMVar_hsa_circ_37225,RMVar_hsa_circ_162678 34844 RMVar_ID_34844 Human_SNP_ID_526086542 A-to-I Human chr13 + 32686638 32686638 32686638 CCTGTTTCTACAAAAAACAAAAATAAAAAATTAGCTAGGTGTGGCATTGTATGCCTGTAGTCCCA CCTGTTTCTACAAAAAACAAAAATAAAAAATTGGCTAGGTGTGGCATTGTATGCCTGTAGTCCCA A G PDS5B Ensembl:ENSG00000083642 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1486676911 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32585,RMVar_hsa_circ_162656,RMVar_hsa_circ_334771,RMVar_hsa_circ_354316,RMVar_hsa_circ_375788,RMVar_hsa_circ_162655,RMVar_hsa_circ_307948,RMVar_hsa_circ_323421,RMVar_hsa_circ_274851,RMVar_hsa_circ_42659,RMVar_hsa_circ_162662,RMVar_hsa_circ_162663,RMVar_hsa_circ_162661,RMVar_hsa_circ_319512,RMVar_hsa_circ_47325,RMVar_hsa_circ_83008,RMVar_hsa_circ_12629,RMVar_hsa_circ_26125,RMVar_hsa_circ_162665,RMVar_hsa_circ_162664,RMVar_hsa_circ_162670,RMVar_hsa_circ_11142,RMVar_hsa_circ_1730,RMVar_hsa_circ_11295,RMVar_hsa_circ_13352,RMVar_hsa_circ_16800,RMVar_hsa_circ_6430,RMVar_hsa_circ_312531,RMVar_hsa_circ_348095,RMVar_hsa_circ_366649,RMVar_hsa_circ_345176,RMVar_hsa_circ_41627,RMVar_hsa_circ_38471,RMVar_hsa_circ_62706,RMVar_hsa_circ_162673,RMVar_hsa_circ_162674,RMVar_hsa_circ_126623,RMVar_hsa_circ_162676,RMVar_hsa_circ_38159,RMVar_hsa_circ_162675,RMVar_hsa_circ_311093,RMVar_hsa_circ_336662,RMVar_hsa_circ_162677,RMVar_hsa_circ_41772,RMVar_hsa_circ_313993,RMVar_hsa_circ_316841,RMVar_hsa_circ_44434,RMVar_hsa_circ_37225,RMVar_hsa_circ_162678 34845 RMVar_ID_34845 Human_SNP_ID_526212423 A-to-I Human chr13 - 33190385 33190385 33190385 ACAGGGTCTTTCTCTGTGACCCTGGCTGGAGTACAGTGATAGGATCATAGCTTACTGCAGCCTCT ACAGGGTCTTTCTCTGTGACCCTGGCTGGAGTGCAGTGATAGGATCATAGCTTACTGCAGCCTCT T C STARD13 Ensembl:ENSG00000133121 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs966206883 Functional Loss SNV dbSNP153 33..33 33 - - - 34846 RMVar_ID_34846 Human_SNP_ID_526325512 A-to-I Human chr13 - 33670318 33670318 33670318 TTAATCTGCCTAGTTGCATTAGCGCTGCCCATATTCTTAATCTTGTCTGCAATGATACCATGAAG TTAATCTGCCTAGTTGCATTAGCGCTGCCCATGTTCTTAATCTTGTCTGCAATGATACCATGAAG T C AL139383.1 Ensembl:ENSG00000230490 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1026999995 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3440567 34847 RMVar_ID_34847 Human_SNP_ID_526644026 A-to-I Human chr13 + 34954908 34954908 34954908 TTCGATCCCCTATTGGTTGAATCTATGGATGTAGAACTCATGGATACAGAGGGTCCACTGTAAAT TTCGATCCCCTATTGGTTGAATCTATGGATGTGGAACTCATGGATACAGAGGGTCCACTGTAAAT A G NBEA Ensembl:ENSG00000172915 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1458913998 Functional Loss SNV dbSNP153 33..33 33 - - - 34848 RMVar_ID_34848 Human_SNP_ID_526711159 A-to-I Human chr13 + 35237212 35237212 35237212 GGGAGATTGAGGCTGCAGTGAGCCACGATCGTACCACTGCACTCCAGCCTGGGCACCGGAGACCC GGGAGATTGAGGCTGCAGTGAGCCACGATCGTGCCACTGCACTCCAGCCTGGGCACCGGAGACCC A G NBEA Ensembl:ENSG00000172915 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs546206319 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9030796 RMVar_hsa_circ_117152,RMVar_hsa_circ_162710,RMVar_hsa_circ_330121,RMVar_hsa_circ_340610,RMVar_hsa_circ_320035,RMVar_hsa_circ_319603,RMVar_hsa_circ_46493,RMVar_hsa_circ_3882,RMVar_hsa_circ_24800,RMVar_hsa_circ_30115,RMVar_hsa_circ_47922,RMVar_hsa_circ_305431,RMVar_hsa_circ_100234,RMVar_hsa_circ_162733,RMVar_hsa_circ_15679,RMVar_hsa_circ_362295,RMVar_hsa_circ_13634,RMVar_hsa_circ_36730,RMVar_hsa_circ_36802,RMVar_hsa_circ_14164,RMVar_hsa_circ_5020,RMVar_hsa_circ_317723,RMVar_hsa_circ_327609,RMVar_hsa_circ_24000,RMVar_hsa_circ_50917,RMVar_hsa_circ_9282,RMVar_hsa_circ_7041,RMVar_hsa_circ_326978,RMVar_hsa_circ_318359,RMVar_hsa_circ_343144,RMVar_hsa_circ_318190,RMVar_hsa_circ_12054,RMVar_hsa_circ_290586,RMVar_hsa_circ_348425,RMVar_hsa_circ_24816,RMVar_hsa_circ_33717,RMVar_hsa_circ_281190,RMVar_hsa_circ_313844,RMVar_hsa_circ_81324,RMVar_hsa_circ_27401,RMVar_hsa_circ_23594,RMVar_hsa_circ_162781,RMVar_hsa_circ_162782,RMVar_hsa_circ_320033,RMVar_hsa_circ_337841,RMVar_hsa_circ_29233 34849 RMVar_ID_34849 Human_SNP_ID_526851656 A-to-I Human chr13 - 35817646 35817646 35817646 CTGGGCCTGGGGTTGACCCAGAGAAGGGATGTACCACTTGGGGCATGGTGATTCTCATCAAATAT CTGGGCCTGGGGTTGACCCAGAGAAGGGATGTGCCACTTGGGGCATGGTGATTCTCATCAAATAT T C DCLK1 Ensembl:ENSG00000133083 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1343393522 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13748,RMVar_hsa_circ_282523,RMVar_hsa_circ_45886,RMVar_hsa_circ_300964,RMVar_hsa_circ_292222,RMVar_hsa_circ_162805,RMVar_hsa_circ_344938,RMVar_hsa_circ_162804,RMVar_hsa_circ_285506,RMVar_hsa_circ_281830,RMVar_hsa_circ_267833,RMVar_hsa_circ_13847,RMVar_hsa_circ_46761,RMVar_hsa_circ_162809,RMVar_hsa_circ_162811,RMVar_hsa_circ_162812,RMVar_hsa_circ_162810,RMVar_hsa_circ_162808,RMVar_hsa_circ_24986,RMVar_hsa_circ_15173,RMVar_hsa_circ_36001 34850 RMVar_ID_34850 Human_SNP_ID_527094884 A-to-I Human chr13 - 36846017 36846017 36846017 AGTTTGGGGCTGTAGTGAACTATGATCATACAACTTCATTCTAGCCTGGGTGACAAAGTGACACC AGTTTGGGGCTGTAGTGAACTATGATCATACAGCTTCATTCTAGCCTGGGTGACAAAGTGACACC T C SMAD9 Ensembl:ENSG00000120693 Protein coding 3'UTR GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1241559582 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17836915,Human_RBP_ID_18268039 34851 RMVar_ID_34851 Human_SNP_ID_527094899 A-to-I Human chr13 - 36846089 36846089 36846089 TGGATGCAGTGGCTCATTCCTATAGTCCCAGCACTTTGGGAGGCCAAGGCGGGAGGATCATCTGA TGGATGCAGTGGCTCATTCCTATAGTCCCAGCGCTTTGGGAGGCCAAGGCGGGAGGATCATCTGA T C SMAD9 Ensembl:ENSG00000120693 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053272281 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4268741 34852 RMVar_ID_34852 Human_SNP_ID_527094900 A-to-I Human chr13 - 36846089 36846089 36846089 TGGATGCAGTGGCTCATTCCTATAGTCCCAGCACTTTGGGAGGCCAAGGCGGGAGGATCATCTGA TGGATGCAGTGGCTCATTCCTATAGTCCCAGCCCTTTGGGAGGCCAAGGCGGGAGGATCATCTGA T G SMAD9 Ensembl:ENSG00000120693 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053272281 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4268741 34853 RMVar_ID_34853 Human_SNP_ID_527125565 A-to-I Human chr13 - 36966664 36966664 36966664 TTAAAAGATCGTGTCTTAAAGAAGCTGGGTATAGTGGCACACGCCTGTGATCCCAGCTGCTCTGT TTAAAAGATCGTGTCTTAAAGAAGCTGGGTATGGTGGCACACGCCTGTGATCCCAGCTGCTCTGT T C ALG5 Ensembl:ENSG00000120697 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1225320839 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_303116,RMVar_hsa_circ_162853,RMVar_hsa_circ_279697,RMVar_hsa_circ_312289,RMVar_hsa_circ_351986,RMVar_hsa_circ_162855,RMVar_hsa_circ_265974,RMVar_hsa_circ_162854 34854 RMVar_ID_34854 Human_SNP_ID_527125566 A-to-I Human chr13 - 36966666 36966666 36966666 TTTTAAAAGATCGTGTCTTAAAGAAGCTGGGTATAGTGGCACACGCCTGTGATCCCAGCTGCTCT TTTTAAAAGATCGTGTCTTAAAGAAGCTGGGTGTAGTGGCACACGCCTGTGATCCCAGCTGCTCT T C ALG5 Ensembl:ENSG00000120697 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs771008211 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_303116,RMVar_hsa_circ_162853,RMVar_hsa_circ_279697,RMVar_hsa_circ_312289,RMVar_hsa_circ_351986,RMVar_hsa_circ_162855,RMVar_hsa_circ_265974,RMVar_hsa_circ_162854 34855 RMVar_ID_34855 Human_SNP_ID_527126271 A-to-I Human chr13 - 36969673 36969673 36969673 AAAACTAGCTGGGTGTGGTGGCGCCCACCTGTAATCCCAGCTACTTGGGAGACTGAGGCAGGAGA AAAACTAGCTGGGTGTGGTGGCGCCCACCTGTGATCCCAGCTACTTGGGAGACTGAGGCAGGAGA T C ALG5 Ensembl:ENSG00000120697 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913589551 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_303116,RMVar_hsa_circ_162853,RMVar_hsa_circ_279697,RMVar_hsa_circ_312289,RMVar_hsa_circ_351986,RMVar_hsa_circ_162855,RMVar_hsa_circ_265974,RMVar_hsa_circ_162854 34856 RMVar_ID_34856 Human_SNP_ID_527126445 A-to-I Human chr13 - 36970452 36970452 36970452 GGGATTACAGGCGTGCGCCACCACACCCAGCTAATTTTTGTATTTTTAGTAGAGGCAGTTTCACC GGGATTACAGGCGTGCGCCACCACACCCAGCTGATTTTTGTATTTTTAGTAGAGGCAGTTTCACC T C ALG5 Ensembl:ENSG00000120697 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1449284456 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_303116,RMVar_hsa_circ_162853,RMVar_hsa_circ_279697,RMVar_hsa_circ_312289,RMVar_hsa_circ_351986,RMVar_hsa_circ_162855,RMVar_hsa_circ_265974,RMVar_hsa_circ_162854 34857 RMVar_ID_34857 Human_SNP_ID_527128994 A-to-I Human chr13 - 36979867 36979867 36979867 AATTGTTTGGTATTTTTAGCAGATGAGGTTTCACCATGTTGCCGAGGCTGGTCTTGAACTCCTGA AATTGTTTGGTATTTTTAGCAGATGAGGTTTCGCCATGTTGCCGAGGCTGGTCTTGAACTCCTGA T C ALG5 Ensembl:ENSG00000120697 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1425305344 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12146331,Human_RBP_ID_17561991 RMVar_hsa_circ_9691,RMVar_hsa_circ_303116,RMVar_hsa_circ_162853,RMVar_hsa_circ_279697,RMVar_hsa_circ_351986,RMVar_hsa_circ_162855,RMVar_hsa_circ_265974 34858 RMVar_ID_34858 Human_SNP_ID_527129115 A-to-I Human chr13 - 36980367 36980367 36980367 AGCCAGGTGTCGTAGCGCACACCTGTAAGCCCAGCTACTCGGGAAGCTGAGGCATGAGAATCACT AGCCAGGTGTCGTAGCGCACACCTGTAAGCCCGGCTACTCGGGAAGCTGAGGCATGAGAATCACT T C ALG5 Ensembl:ENSG00000120697 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1426763912 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9691,RMVar_hsa_circ_303116,RMVar_hsa_circ_162853,RMVar_hsa_circ_279697,RMVar_hsa_circ_351986,RMVar_hsa_circ_162855,RMVar_hsa_circ_265974 34859 RMVar_ID_34859 Human_SNP_ID_527136483 A-to-I Human chr13 - 37009639 37009639 37009639 GTCTTGCATTACTTTTTGTTCCTTTTTTAAAAACACAAGAGCACTGAATCAAAAGAATTGAGTTT GTCTTGCATTACTTTTTGTTCCTTTTTTAAAAGCACAAGAGCACTGAATCAAAAGAATTGAGTTT T C SUPT20H Ensembl:ENSG00000102710 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs11559100 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_435551,Human_RBP_ID_3428513,Human_RBP_ID_6277322,Human_RBP_ID_12146991,Human_RBP_ID_17244668,Human_RBP_ID_18639590,Human_RBP_ID_25045992,Human_RBP_ID_27558533 34860 RMVar_ID_34860 Human_SNP_ID_527138646 A-to-I Human chr13 - 37018759 37018759 37018759 CCTGCTACTCAAGAGGCTGAGGTCGGAGGATCACTTGAGCCCAGGAAGTCGAGGCTGCAGTGAGC CCTGCTACTCAAGAGGCTGAGGTCGGAGGATCCCTTGAGCCCAGGAAGTCGAGGCTGCAGTGAGC T G SUPT20H Ensembl:ENSG00000102710 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941103844 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_278434,RMVar_hsa_circ_341021,RMVar_hsa_circ_58334,RMVar_hsa_circ_90668,RMVar_hsa_circ_39458,RMVar_hsa_circ_25972,RMVar_hsa_circ_162858,RMVar_hsa_circ_162859,RMVar_hsa_circ_49237 34861 RMVar_ID_34861 Human_SNP_ID_527150527 A-to-I Human chr13 + 37068291 37068291 37068291 ATCCAGCAATTCTACTTCTAGGTATATACTCAAAGGAATTGAAAGCTGGGACTTGAACAGATATT ATCCAGCAATTCTACTTCTAGGTATATACTCAGAGGAATTGAAAGCTGGGACTTGAACAGATATT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215435879 Functional Loss SNV dbSNP153 33..33 33 - - - 34862 RMVar_ID_34862 Human_SNP_ID_527173386 A-to-I Human chr13 + 37166499 37166499 37166499 TACCCTTGACTGAAGACCGGTCCTTCTTTATCAGGGATGGTCATCCTCTTCGACCGAGTGCGCAG TACCCTTGACTGAAGACCGGTCCTTCTTTATCGGGGATGGTCATCCTCTTCGACCGAGTGCGCAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223359630 Functional Loss SNV dbSNP153 33..33 33 - - - 34863 RMVar_ID_34863 Human_SNP_ID_527370486 A-to-I Human chr13 - 37979121 37979121 37979121 TAAACAGCTCTAAAAACTGTGAACAAAATACAAAATTCATAAAACAACTCCCTAAACACTCTGGA TAAACAGCTCTAAAAACTGTGAACAAAATACACAATTCATAAAACAACTCCCTAAACACTCTGGA T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978021161 Functional Loss SNV dbSNP153 33..33 33 - - - 34864 RMVar_ID_34864 Human_SNP_ID_527713873 A-to-I Human chr13 - 39378528 39378528 39378528 ACTGGTAAAGCCCTCTTGTCTTATCTCTTTGCAGGCTTGTTGATTGGTGCTGGCTGTGCCCTCTA ACTGGTAAAGCCCTCTTGTCTTATCTCTTTGCGGGCTTGTTGATTGGTGCTGGCTGTGCCCTCTA T C LHFPL6 Ensembl:ENSG00000183722 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1025520867 Functional Loss SNV dbSNP153 33..33 33 - - - 34865 RMVar_ID_34865 Human_SNP_ID_527731638 A-to-I Human chr13 - 39457075 39457075 39457075 TCTAATTTGGCCAAGTGCTGTGGCTCACGTCTATAATCCCAGCAGTTTTGGAGGCCGAGGCTGGC TCTAATTTGGCCAAGTGCTGTGGCTCACGTCTGTAATCCCAGCAGTTTTGGAGGCCGAGGCTGGC T C LHFPL6 Ensembl:ENSG00000183722 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1304588220 Functional Loss SNV dbSNP153 33..33 33 - - - 34866 RMVar_ID_34866 Human_SNP_ID_527737755 A-to-I Human chr13 - 39484146 39484146 39484146 GCTCTGTGAATCTGAAACCGGGTGGAGAAGATAGGATTGGGGAAAAACTTGGAAATGATTGTCAC GCTCTGTGAATCTGAAACCGGGTGGAGAAGATGGGATTGGGGAAAAACTTGGAAATGATTGTCAC T C LHFPL6 Ensembl:ENSG00000183722 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1395082643 Functional Loss SNV dbSNP153 33..33 33 - - - 34867 RMVar_ID_34867 Human_SNP_ID_527745628 A-to-I Human chr13 - 39519001 39519001 39519001 AAACTCCTGACCTCAAGTGATCTACCACCTCAACCTCCCAAAGTTCTGGAATTACAGGTGTGAGC AAACTCCTGACCTCAAGTGATCTACCACCTCAGCCTCCCAAAGTTCTGGAATTACAGGTGTGAGC T C LHFPL6 Ensembl:ENSG00000183722 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs556358293 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22915986 34868 RMVar_ID_34868 Human_SNP_ID_527745629 A-to-I Human chr13 - 39519001 39519001 39519001 AAACTCCTGACCTCAAGTGATCTACCACCTCAACCTCCCAAAGTTCTGGAATTACAGGTGTGAGC AAACTCCTGACCTCAAGTGATCTACCACCTCACCCTCCCAAAGTTCTGGAATTACAGGTGTGAGC T G LHFPL6 Ensembl:ENSG00000183722 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs556358293 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22915986 34869 RMVar_ID_34869 Human_SNP_ID_527748129 A-to-I Human chr13 - 39529934 39529934 39529934 GATGAACTTCAGAATAAAATTTTCTCTTTCATAAAACCTTTTTCTTCTTGACACTTCGTGCAAAA GATGAACTTCAGAATAAAATTTTCTCTTTCATGAAACCTTTTTCTTCTTGACACTTCGTGCAAAA T C LHFPL6 Ensembl:ENSG00000183722 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs757561558 Functional Loss SNV dbSNP153 33..33 33 - - - 34870 RMVar_ID_34870 Human_SNP_ID_527748313 A-to-I Human chr13 - 39530682 39530682 39530682 AAAAGTGATAATGTAAAAGACATTTTGTACAAAGTGTCAAGAAGGAAAAGGTTTTATGAAACACG AAAAGTGATAATGTAAAAGACATTTTGTACAATGTGTCAAGAAGGAAAAGGTTTTATGAAACACG T A LHFPL6 Ensembl:ENSG00000183722 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1490679738 Functional Loss SNV dbSNP153 33..33 33 - - - 34871 RMVar_ID_34871 Human_SNP_ID_527748319 A-to-I Human chr13 - 39530711 39530710 39530711 TAAGCAACCACAGCACAATGCAAAAGAAAAAAAGTGATAATGTAAAAGACATTTTGTACAAAGTG TAAGCAACCACAGCACAATGCAAAAGAAAAAA_GTGATAATGTAAAAGACATTTTGTACAAAGTG CT C LHFPL6 Ensembl:ENSG00000183722 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs376065201 Functional Loss DEL dbSNP153 33..33 33 - - - 34872 RMVar_ID_34872 Human_SNP_ID_527758994 A-to-I Human chr13 - 39575030 39575030 39575030 GAGTTTGCTCTGTCGCGAGGCCAAAGTGCAGTAGCGCTATCTCGGCTCACTGCAACCTCTGCCTC GAGTTTGCTCTGTCGCGAGGCCAAAGTGCAGTGGCGCTATCTCGGCTCACTGCAACCTCTGCCTC T C LHFPL6 Ensembl:ENSG00000183722 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1453057195 Functional Loss SNV dbSNP153 33..33 33 - - - 34873 RMVar_ID_34873 Human_SNP_ID_527972556 A-to-I Human chr13 - 40456103 40456103 40456103 TGCACCACCACGCCTGGCTAATTTGTATTCTTAGTAGAGACGGGGTTTGACCATGTTGGCCAGGC TGCACCACCACGCCTGGCTAATTTGTATTCTTTGTAGAGACGGGGTTTGACCATGTTGGCCAGGC T A LINC00598 Ensembl:ENSG00000215483 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1246912863 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5246702 RMVar_hsa_circ_67097,RMVar_hsa_circ_125302,RMVar_hsa_circ_73309,RMVar_hsa_circ_162912 34874 RMVar_ID_34874 Human_SNP_ID_528016236 A-to-I Human chr13 - 40641864 40641864 40641864 CTCTCACCTCAGCCTCCCAAGTAGCTGGGATTACAAGTATGCGCCACCATGCCCTGCTAATTTTT CTCTCACCTCAGCCTCCCAAGTAGCTGGGATTGCAAGTATGCGCCACCATGCCCTGCTAATTTTT T C FOXO1 Ensembl:ENSG00000150907 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs533801358 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99843,RMVar_hsa_circ_162915 34875 RMVar_ID_34875 Human_SNP_ID_528021261 A-to-I Human chr13 - 40661338 40661338 40661338 CTAGAAGGCGGAGGTTGCAGTGAGCCGAGATCACGTCACTGACCTCCAACCTGGGCAACAGAGGG CTAGAAGGCGGAGGTTGCAGTGAGCCGAGATCGCGTCACTGACCTCCAACCTGGGCAACAGAGGG T C FOXO1 Ensembl:ENSG00000150907 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1356859019 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25078318 34876 RMVar_ID_34876 Human_SNP_ID_528021279 A-to-I Human chr13 - 40661416 40661416 40661416 GGCAGGTGCCTGTAGTCCCAGCTATCGTGCCAATAATCCCAACTACTCGGGAGGCTGAGGCAGGA GGCAGGTGCCTGTAGTCCCAGCTATCGTGCCAGTAATCCCAACTACTCGGGAGGCTGAGGCAGGA T C FOXO1 Ensembl:ENSG00000150907 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170190081 Functional Loss SNV dbSNP153 33..33 33 - - - 34877 RMVar_ID_34877 Human_SNP_ID_528038263 A-to-I Human chr13 - 40728362 40728362 40728362 CTCCTGCTTCAGCCCCTCAAGTAGCTGGTATTACAGGTGCCCACCACCACACCCAGCTAATTTTT CTCCTGCTTCAGCCCCTCAAGTAGCTGGTATTGCAGGTGCCCACCACCACACCCAGCTAATTTTT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215879358 Functional Loss SNV dbSNP153 33..33 33 - - - 34878 RMVar_ID_34878 Human_SNP_ID_528057765 A-to-I Human chr13 + 40810346 40810346 40810346 ATGTCCAGCTAATTTTTTTTGGTATTTTTTGTAGAGACGAGGTTTCACCATGTTGTCCAGGTTGG ATGTCCAGCTAATTTTTTTTGGTATTTTTTGTGGAGACGAGGTTTCACCATGTTGTCCAGGTTGG A G SLC25A15 Ensembl:ENSG00000102743 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1240226990 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75703,RMVar_hsa_circ_162920 34879 RMVar_ID_34879 Human_SNP_ID_528082495 A-to-I Human chr13 - 40913497 40913497 40913497 CTTTAAAAATTATTCTGATGAAGAATCTGGATAGGGAAAAACTGAAGACTTTTTTTTTTAGACGA CTTTAAAAATTATTCTGATGAAGAATCTGGATGGGGAAAAACTGAAGACTTTTTTTTTTAGACGA T C TPTE2P5,SUGT1P3 Ensembl:ENSG00000168852,Ensembl:ENSG00000239827 Pseudogene,Pseudogene intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1340277501 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_272990 34880 RMVar_ID_34880 Human_SNP_ID_528083784 A-to-I Human chr13 - 40920111 40920111 40920111 CATGTCTGTAATCCCAGCACTTTGGGAGGCCAAGTGGGGCGGATCGCTTGAGGTTAGGAGTTGGA CATGTCTGTAATCCCAGCACTTTGGGAGGCCAGGTGGGGCGGATCGCTTGAGGTTAGGAGTTGGA T C TPTE2P5,SUGT1P3 Ensembl:ENSG00000168852,Ensembl:ENSG00000239827 Pseudogene,Pseudogene intron,intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1482171054 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17360857 34881 RMVar_ID_34881 Human_SNP_ID_528087496 A-to-I Human chr13 - 40934619 40934619 40934619 GGTCAGGACTTTGAGACCAGCCTGACCAACATAGAAAACCCCATCTCAATTAAAACTACAAAAAT GGTCAGGACTTTGAGACCAGCCTGACCAACATGGAAAACCCCATCTCAATTAAAACTACAAAAAT T C ELF1 Ensembl:ENSG00000120690 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1458116481 Functional Loss SNV dbSNP153 33..33 33 - - - 34882 RMVar_ID_34882 Human_SNP_ID_528087766 A-to-I Human chr13 - 40935813 40935813 40935813 AAAAAATTAGCTGGGCATGGTGGCGGGTGCCTATAATCCCAGCTACTCGGGAGGCTGAGGCAGAG AAAAAATTAGCTGGGCATGGTGGCGGGTGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGAG T C ELF1 Ensembl:ENSG00000120690 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1445687054 Functional Loss SNV dbSNP153 33..33 33 - - - 34883 RMVar_ID_34883 Human_SNP_ID_528087935 A-to-I Human chr13 - 40936503 40936503 40936503 GTGATCCACCCACCTTGGACTCCCAAAGTGCTAGGATTACAGGCATGAGCCACCGTGCCCGGCCA GTGATCCACCCACCTTGGACTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGTGCCCGGCCA T C ELF1 Ensembl:ENSG00000120690 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1303063858 Functional Loss SNV dbSNP153 33..33 33 - - - 34884 RMVar_ID_34884 Human_SNP_ID_528087952 A-to-I Human chr13 - 40936587 40936587 40936587 CCGACTATGCCCAGCTAATTTTTGTATTTTTAATAGAGATGGGGTTTCACCATGTTGACCAGGCC CCGACTATGCCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGACCAGGCC T C ELF1 Ensembl:ENSG00000120690 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1566163736 Functional Loss SNV dbSNP153 33..33 33 - - - 34885 RMVar_ID_34885 Human_SNP_ID_528088057 A-to-I Human chr13 - 40936825 40936825 40936825 CTCCTGCCTCAGCCTCCCGAGTTGCTGGGATTATAGGCACGCGCCACCATGCCCAGCTAATTTTT CTCCTGCCTCAGCCTCCCGAGTTGCTGGGATTGTAGGCACGCGCCACCATGCCCAGCTAATTTTT T C ELF1 Ensembl:ENSG00000120690 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1292330473 Functional Loss SNV dbSNP153 33..33 33 - - - 34886 RMVar_ID_34886 Human_SNP_ID_528088074 A-to-I Human chr13 - 40936910 40936910 40936910 TCCCTCTGTAGCCCAGGCTGGAGTGCAGTGGCACGATCTCACTCACACTGCTCCCTTCACCTCCC TCCCTCTGTAGCCCAGGCTGGAGTGCAGTGGCGCGATCTCACTCACACTGCTCCCTTCACCTCCC T C ELF1 Ensembl:ENSG00000120690 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1279638160 Functional Loss SNV dbSNP153 33..33 33 - - - 34887 RMVar_ID_34887 Human_SNP_ID_528088225 A-to-I Human chr13 - 40937630 40937630 40937630 CCCGACTCTACTAAAAATACAAAAAATTAGCTAGGCGTAGTGGCGGGCGCCTGTAATCCCAGCTA CCCGACTCTACTAAAAATACAAAAAATTAGCTGGGCGTAGTGGCGGGCGCCTGTAATCCCAGCTA T C ELF1 Ensembl:ENSG00000120690 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs765052127 Functional Loss SNV dbSNP153 33..33 33 - - - 34888 RMVar_ID_34888 Human_SNP_ID_528088310 A-to-I Human chr13 - 40937954 40937954 40937954 AAATTAGCTGGGTATGGTGGCAGGCACCTGTAATCCTAGCTACTCAGGAGGCTGAGGCAGGAGAA AAATTAGCTGGGTATGGTGGCAGGCACCTGTACTCCTAGCTACTCAGGAGGCTGAGGCAGGAGAA T G ELF1 Ensembl:ENSG00000120690 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1322245101 Functional Loss SNV dbSNP153 33..33 33 - - - 34889 RMVar_ID_34889 Human_SNP_ID_528091449 A-to-I Human chr13 - 40951694 40951692 40951694 CCCAGCTAATTTTTTGTATTTTTAGTAGAAACAGGGTTTCTCCATGTTGGCCAGTCTCAGACTCC CCCAGCTAATTTTTTGTATTTTTAGTAGAAAC__GGTTTCTCCATGTTGGCCAGTCTCAGACTCC CCT C ELF1 Ensembl:ENSG00000120690 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1209250024 Functional Loss DEL dbSNP153 33..34 33 - - - Human_Splice_Rec_1459446 RMVar_hsa_circ_350593,RMVar_hsa_circ_354621,RMVar_hsa_circ_353900,RMVar_hsa_circ_364736 34890 RMVar_ID_34890 Human_SNP_ID_528091466 A-to-I Human chr13 - 40951745 40951745 40951745 CTCCTATCTCACTCTCCTGAGTAGCTGGGACTACAGGTGCGTGCCACCACGCCCAGCTAATTTTT CTCCTATCTCACTCTCCTGAGTAGCTGGGACTGCAGGTGCGTGCCACCACGCCCAGCTAATTTTT T C ELF1 Ensembl:ENSG00000120690 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1411674511 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_350593,RMVar_hsa_circ_354621,RMVar_hsa_circ_353900,RMVar_hsa_circ_364736 34891 RMVar_ID_34891 Human_SNP_ID_528111415 A-to-I Human chr13 - 41036033 41036033 41036033 GGGCGTGGTGGCGGGCACCTGTGGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATGGCGTGAA GGGCGTGGTGGCGGGCACCTGTGGTCCCAGCTGCTTGGGAGGCTGAGGCAGGAGAATGGCGTGAA T C ELF1 Ensembl:ENSG00000120690 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs890109385 Functional Loss SNV dbSNP153 33..33 33 - - - 34892 RMVar_ID_34892 Human_SNP_ID_528115989 A-to-I Human chr13 - 41053294 41053294 41053294 GCTGGAGTGCAGTAGCATGATCTCGGCTCACTACAAGCTCTGCCTCCCGGGTTCAAGCAATTCTC GCTGGAGTGCAGTAGCATGATCTCGGCTCACTGCAAGCTCTGCCTCCCGGGTTCAAGCAATTCTC T C ELF1 Ensembl:ENSG00000120690 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs537253933 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25048751 34893 RMVar_ID_34893 Human_SNP_ID_528123084 A-to-I Human chr13 + 41077371 41077371 41077371 ATATGAGGCCGAGTGCGGTGCCTCATGCCTGTAATCTCAGCACTTTGGGAGGCTGAGGCAGGAGA ATATGAGGCCGAGTGCGGTGCCTCATGCCTGTCATCTCAGCACTTTGGGAGGCTGAGGCAGGAGA A C WBP4 Ensembl:ENSG00000120688 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1254723961 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59098,RMVar_hsa_circ_75026,RMVar_hsa_circ_358352,RMVar_hsa_circ_162933 34894 RMVar_ID_34894 Human_SNP_ID_528145423 A-to-I Human chr13 - 41171127 41171127 41171127 GCGCTTGCAGCATGGCTGACCAACTGACTGAAAGGCAGACTGCAGAATTCAAAGAAGCTTTTTCA GCGCTTGCAGCATGGCTGACCAACTGACTGAAGGGCAGACTGCAGAATTCAAAGAAGCTTTTTCA T C CALM2P3 Ensembl:ENSG00000215482 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878858794 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1484123,Human_RBP_ID_4278898,Human_RBP_ID_18527856,Human_RBP_ID_23595395 Human_miRNA_ID_1860385 34895 RMVar_ID_34895 Human_SNP_ID_528155585 A-to-I Human chr13 - 41216610 41216610 41216610 GAAGGGCCAAAGGGGGAAGATCTCTTGAGGTAAGAATTTGAGACCAGCCTGGGCAAAATAGACCC GAAGGGCCAAAGGGGGAAGATCTCTTGAGGTATGAATTTGAGACCAGCCTGGGCAAAATAGACCC T A MTRF1 Ensembl:ENSG00000120662 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1249384467 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_436091 RMVar_hsa_circ_86304 34896 RMVar_ID_34896 Human_SNP_ID_528158541 A-to-I Human chr13 - 41230014 41230014 41230014 TCACTGCAACCTCTGCCTCCAGTGTTCAAGCTATTCTCCTGCATCAGCCTCCCAGGTAGCTGGGA TCACTGCAACCTCTGCCTCCAGTGTTCAAGCTCTTCTCCTGCATCAGCCTCCCAGGTAGCTGGGA T G MTRF1 Ensembl:ENSG00000120662 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs191863422 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_311761,RMVar_hsa_circ_332064,RMVar_hsa_circ_86304,RMVar_hsa_circ_341757,RMVar_hsa_circ_329534,RMVar_hsa_circ_267347,RMVar_hsa_circ_55310,RMVar_hsa_circ_162937,RMVar_hsa_circ_358545 34897 RMVar_ID_34897 Human_SNP_ID_528160699 A-to-I Human chr13 - 41239978 41239978 41239978 TTTTGTATTTTTAGTAGAGACAGGTTTTCACCATGTTGGCCAGACTGGTCTCGAACTCCTGACCT TTTTGTATTTTTAGTAGAGACAGGTTTTCACCTTGTTGGCCAGACTGGTCTCGAACTCCTGACCT T A MTRF1 Ensembl:ENSG00000120662 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs532338915 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_311761,RMVar_hsa_circ_332064,RMVar_hsa_circ_86304,RMVar_hsa_circ_329534,RMVar_hsa_circ_267347,RMVar_hsa_circ_351806,RMVar_hsa_circ_55310,RMVar_hsa_circ_162937,RMVar_hsa_circ_360621,RMVar_hsa_circ_376440,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 34898 RMVar_ID_34898 Human_SNP_ID_528160700 A-to-I Human chr13 - 41239978 41239978 41239978 TTTTGTATTTTTAGTAGAGACAGGTTTTCACCATGTTGGCCAGACTGGTCTCGAACTCCTGACCT TTTTGTATTTTTAGTAGAGACAGGTTTTCACCGTGTTGGCCAGACTGGTCTCGAACTCCTGACCT T C MTRF1 Ensembl:ENSG00000120662 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs532338915 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_311761,RMVar_hsa_circ_332064,RMVar_hsa_circ_86304,RMVar_hsa_circ_329534,RMVar_hsa_circ_267347,RMVar_hsa_circ_351806,RMVar_hsa_circ_55310,RMVar_hsa_circ_162937,RMVar_hsa_circ_360621,RMVar_hsa_circ_376440,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 34899 RMVar_ID_34899 Human_SNP_ID_528180358 A-to-I Human chr13 + 41321204 41321204 41321204 CCTGCAGTCCCAGCTATCCAGGATGTTGAGGCAGGAGGATCCCTTGAACCTAAGAGTTGAGGCTG CCTGCAGTCCCAGCTATCCAGGATGTTGAGGCCGGAGGATCCCTTGAACCTAAGAGTTGAGGCTG A C NAA16 Ensembl:ENSG00000172766 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886221549 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12156884 RMVar_hsa_circ_9863,RMVar_hsa_circ_271693,RMVar_hsa_circ_292416,RMVar_hsa_circ_83047,RMVar_hsa_circ_269971,RMVar_hsa_circ_66493,RMVar_hsa_circ_162964,RMVar_hsa_circ_162953,RMVar_hsa_circ_162955,RMVar_hsa_circ_162957,RMVar_hsa_circ_2832,RMVar_hsa_circ_162958,RMVar_hsa_circ_162956,RMVar_hsa_circ_162954,RMVar_hsa_circ_22701,RMVar_hsa_circ_323089,RMVar_hsa_circ_334567,RMVar_hsa_circ_341283,RMVar_hsa_circ_323270,RMVar_hsa_circ_319630,RMVar_hsa_circ_273687,RMVar_hsa_circ_280423,RMVar_hsa_circ_48513,RMVar_hsa_circ_162966,RMVar_hsa_circ_162967,RMVar_hsa_circ_162968,RMVar_hsa_circ_162965,RMVar_hsa_circ_162962,RMVar_hsa_circ_162963,RMVar_hsa_circ_162961,RMVar_hsa_circ_162970,RMVar_hsa_circ_323930,RMVar_hsa_circ_337635,RMVar_hsa_circ_349976,RMVar_hsa_circ_336328,RMVar_hsa_circ_73597,RMVar_hsa_circ_162969 34900 RMVar_ID_34900 Human_SNP_ID_528185747 A-to-I Human chr13 + 41341462 41341462 41341462 ACAACTTGCCAGCCGTGGTGGCTCATGCCTGTAATCCAGCACTTTGGGAGGCTGAGGTGGGAGGA ACAACTTGCCAGCCGTGGTGGCTCATGCCTGTGATCCAGCACTTTGGGAGGCTGAGGTGGGAGGA A G NAA16 Ensembl:ENSG00000172766 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1017321589 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83047,RMVar_hsa_circ_66493,RMVar_hsa_circ_162953,RMVar_hsa_circ_22701,RMVar_hsa_circ_334567,RMVar_hsa_circ_341283,RMVar_hsa_circ_323270,RMVar_hsa_circ_48513,RMVar_hsa_circ_162966,RMVar_hsa_circ_162967,RMVar_hsa_circ_162968,RMVar_hsa_circ_162965,RMVar_hsa_circ_323930,RMVar_hsa_circ_336328,RMVar_hsa_circ_73597,RMVar_hsa_circ_313757,RMVar_hsa_circ_162969,RMVar_hsa_circ_265122,RMVar_hsa_circ_20113,RMVar_hsa_circ_23235,RMVar_hsa_circ_65558,RMVar_hsa_circ_75491,RMVar_hsa_circ_294891,RMVar_hsa_circ_20942,RMVar_hsa_circ_162975 34901 RMVar_ID_34901 Human_SNP_ID_528186031 A-to-I Human chr13 + 41342347 41342347 41342347 TTTAGTAGAGACAGGGTTTCCTCGTGTTGCCCAGGCTGGTCTCGAACTCCTGAGCGCAAGCAATC TTTAGTAGAGACAGGGTTTCCTCGTGTTGCCCGGGCTGGTCTCGAACTCCTGAGCGCAAGCAATC A G NAA16 Ensembl:ENSG00000172766 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1343863501 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83047,RMVar_hsa_circ_66493,RMVar_hsa_circ_162953,RMVar_hsa_circ_22701,RMVar_hsa_circ_334567,RMVar_hsa_circ_341283,RMVar_hsa_circ_323270,RMVar_hsa_circ_48513,RMVar_hsa_circ_162966,RMVar_hsa_circ_162967,RMVar_hsa_circ_162968,RMVar_hsa_circ_162965,RMVar_hsa_circ_323930,RMVar_hsa_circ_336328,RMVar_hsa_circ_73597,RMVar_hsa_circ_313757,RMVar_hsa_circ_162969,RMVar_hsa_circ_265122,RMVar_hsa_circ_20113,RMVar_hsa_circ_23235,RMVar_hsa_circ_65558,RMVar_hsa_circ_75491,RMVar_hsa_circ_294891,RMVar_hsa_circ_20942,RMVar_hsa_circ_162975 34902 RMVar_ID_34902 Human_SNP_ID_528246893 A-to-I Human chr13 - 41573849 41573849 41573849 GGGAGGCCGAGGCGGGCAGACCACCTGAGGCCAGGAGCTCGATACCAGCCCGGCCAACCTGGCGA GGGAGGCCGAGGCGGGCAGACCACCTGAGGCCGGGAGCTCGATACCAGCCCGGCCAACCTGGCGA T C VWA8 Ensembl:ENSG00000102763 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1456586010 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80270,RMVar_hsa_circ_162981 34903 RMVar_ID_34903 Human_SNP_ID_528246894 A-to-I Human chr13 - 41573864 41573864 41573864 CAATCCCAGCACCCCGGGAGGCCGAGGCGGGCAGACCACCTGAGGCCAGGAGCTCGATACCAGCC CAATCCCAGCACCCCGGGAGGCCGAGGCGGGCGGACCACCTGAGGCCAGGAGCTCGATACCAGCC T C VWA8 Ensembl:ENSG00000102763 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1260293546 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80270,RMVar_hsa_circ_162981 34904 RMVar_ID_34904 Human_SNP_ID_528328145 A-to-I Human chr13 + 41926641 41926641 41926641 TATGCAGACTACCACAATCTCTTGGAAATCACAGAGAAGATGGTTTCAGGGATGGTAAAGCATAT TATGCAGACTACCACAATCTCTTGGAAATCACGGAGAAGATGGTTTCAGGGATGGTAAAGCATAT A G KARS1P1 Ensembl:ENSG00000229696 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048568678 Functional Loss SNV dbSNP153 33..33 33 - - - 34905 RMVar_ID_34905 Human_SNP_ID_528328152 A-to-I Human chr13 + 41926665 41926665 41926665 GAAATCACAGAGAAGATGGTTTCAGGGATGGTAAAGCATATTACAGGCAGTTACAAGGTCAGCTA GAAATCACAGAGAAGATGGTTTCAGGGATGGTGAAGCATATTACAGGCAGTTACAAGGTCAGCTA A G KARS1P1 Ensembl:ENSG00000229696 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1004435316 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8249070,Human_RBP_ID_18527953 34906 RMVar_ID_34906 Human_SNP_ID_528328209 A-to-I Human chr13 - 41926892 41926892 41926892 TACAAGCTTGTCAAGGAGCCTGGCTGTGGTCCAAGGTAGAGGGCATTCAACAGCTTTTGCCACAC TACAAGCTTGTCAAGGAGCCTGGCTGTGGTCCGAGGTAGAGGGCATTCAACAGCTTTTGCCACAC T C VWA8 Ensembl:ENSG00000102763 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202697272 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73832,RMVar_hsa_circ_55717,RMVar_hsa_circ_277963,RMVar_hsa_circ_163040,RMVar_hsa_circ_9254,RMVar_hsa_circ_328749,RMVar_hsa_circ_163042,RMVar_hsa_circ_57145,RMVar_hsa_circ_124599,RMVar_hsa_circ_281815,RMVar_hsa_circ_163046,RMVar_hsa_circ_163047 34907 RMVar_ID_34907 Human_SNP_ID_528431022 A-to-I Human chr13 - 42369390 42369390 42369390 AAAAGGTCAAGTCCATTGTGACACTGGATGGAAGCAAACTTTTTCACCTGCAGAAGTGTAACGGG AAAAGGTCAAGTCCATTGTGACACTGGATGGAGGCAAACTTTTTCACCTGCAGAAGTGTAACGGG T C FABP3P2 Ensembl:ENSG00000233259 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs897586916 Functional Loss SNV dbSNP153 33..33 33 - - - 34908 RMVar_ID_34908 Human_SNP_ID_528431028 A-to-I Human chr13 - 42369421 42369421 42369421 ATGGGGTTCGATGAGACAACAGCAGATGACAAAAAGGTCAAGTCCATTGTGACACTGGATGGAAG ATGGGGTTCGATGAGACAACAGCAGATGACAAGAAGGTCAAGTCCATTGTGACACTGGATGGAAG T C FABP3P2 Ensembl:ENSG00000233259 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs111474103 Functional Loss SNV dbSNP153 33..33 33 - - - 34909 RMVar_ID_34909 Human_SNP_ID_528431029 A-to-I Human chr13 - 42369422 42369422 42369422 GATGGGGTTCGATGAGACAACAGCAGATGACAAAAAGGTCAAGTCCATTGTGACACTGGATGGAA GATGGGGTTCGATGAGACAACAGCAGATGACAGAAAGGTCAAGTCCATTGTGACACTGGATGGAA T C FABP3P2 Ensembl:ENSG00000233259 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs113367059 Functional Loss SNV dbSNP153 33..33 33 - - - 34910 RMVar_ID_34910 Human_SNP_ID_528593076 A-to-I Human chr13 + 43034522 43034522 43034522 AATTTTTAGTAGAGACGGGGTTTCCCCGTGTTAGCCAGGATGGTCTTGTTCTCCTGACCTAGTGA AATTTTTAGTAGAGACGGGGTTTCCCCGTGTTGGCCAGGATGGTCTTGTTCTCCTGACCTAGTGA A G DNAJC15 Ensembl:ENSG00000120675 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1019865027 Functional Loss SNV dbSNP153 33..33 33 - - - 34911 RMVar_ID_34911 Human_SNP_ID_528722210 A-to-I Human chr13 - 43590585 43590584 43590585 TTTTTTTAGTAGAAACAAGGTTTCACCATGTTAGCCACAATGGTCTCGATCTCCTGACCTCCTGA TTTTTTTAGTAGAAACAAGGTTTCACCATGTT_GCCACAATGGTCTCGATCTCCTGACCTCCTGA CT C ENOX1 Ensembl:ENSG00000120658 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215718289 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_113052,RMVar_hsa_circ_8541,RMVar_hsa_circ_163111,RMVar_hsa_circ_317997,RMVar_hsa_circ_312123,RMVar_hsa_circ_312649,RMVar_hsa_circ_22010 34912 RMVar_ID_34912 Human_SNP_ID_528764170 A-to-I Human chr13 - 43772649 43772643 43772649 TGCCTTCTGGGTTCATGTGATTCTCTTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGTGTGTA TGCCTTCTGGGTTCATGTGATTCTCTTGCCTC______CCGAGTAGCTGGGATTACAGGTGTGTA GGAGGCT G ENOX1 Ensembl:ENSG00000120658 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1294732703 Functional Loss DEL dbSNP153 33..38 33 - - - 34913 RMVar_ID_34913 Human_SNP_ID_528915951 A-to-I Human chr13 - 44434447 44434447 44434447 CAGTATTAAACACTCATATGCTTATGGCTTGGAGAAATTTCTTAGTTGGGTGAATTAAAGGTTAA CAGTATTAAACACTCATATGCTTATGGCTTGGGGAAATTTCTTAGTTGGGTGAATTAAAGGTTAA T C TSC22D1 Ensembl:ENSG00000102804 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1288545999 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_996549,Human_RBP_ID_2383786,Human_RBP_ID_18177276,Human_RBP_ID_24469577 Human_miRNA_ID_1539678,Human_miRNA_ID_1593654 34914 RMVar_ID_34914 Human_SNP_ID_528943649 A-to-I Human chr13 - 44547882 44547882 44547882 GGGTAGCTGAGACAGGAGGATTGCTTGAGCCCAGGAGTTCGAGGCTGTAGTGTGCCGTGATTGTA GGGTAGCTGAGACAGGAGGATTGCTTGAGCCCGGGAGTTCGAGGCTGTAGTGTGCCGTGATTGTA T C TSC22D1 Ensembl:ENSG00000102804 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs938849040 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12162568 34915 RMVar_ID_34915 Human_SNP_ID_528947631 A-to-I Human chr13 - 44563057 44563057 44563057 TCTCGTTGCCCAGGCTGGAGTGCAATGATGCAATCTTGGCTCATTGCAACCTTCCCCTCGCGGGT TCTCGTTGCCCAGGCTGGAGTGCAATGATGCAGTCTTGGCTCATTGCAACCTTCCCCTCGCGGGT T C TSC22D1 Ensembl:ENSG00000102804 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs570289625 Functional Loss SNV dbSNP153 33..33 33 - - - 34916 RMVar_ID_34916 Human_SNP_ID_528947633 A-to-I Human chr13 - 44563065 44563065 44563065 AGTTTTGTTCTCGTTGCCCAGGCTGGAGTGCAATGATGCAATCTTGGCTCATTGCAACCTTCCCC AGTTTTGTTCTCGTTGCCCAGGCTGGAGTGCAGTGATGCAATCTTGGCTCATTGCAACCTTCCCC T C TSC22D1 Ensembl:ENSG00000102804 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs537625163 Functional Loss SNV dbSNP153 33..33 33 - - - 34917 RMVar_ID_34917 Human_SNP_ID_529049908 A-to-I Human chr13 - 44983702 44983702 44983702 GCCTCAACCTGCTGGGCTCAAGTGATTCTCCCATCTCAGCCTCACAAGTAGCTGGGACTACAGGC GCCTCAACCTGCTGGGCTCAAGTGATTCTCCCGTCTCAGCCTCACAAGTAGCTGGGACTACAGGC T C AL359706.1,NUFIP1 Ensembl:ENSG00000223732,Ensembl:ENSG00000083635 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1021580887 Functional Loss SNV dbSNP153 33..33 33 - - - 34918 RMVar_ID_34918 Human_SNP_ID_529050726 A-to-I Human chr13 - 44987001 44987001 44987001 TGCCTGGGCAACAAAGTGAGACCCCCGTCTCTACAAAAAAAATAAAATTAGCCAGGCGTGGTGGA TGCCTGGGCAACAAAGTGAGACCCCCGTCTCTGCAAAAAAAATAAAATTAGCCAGGCGTGGTGGA T C AL359706.1,NUFIP1 Ensembl:ENSG00000223732,Ensembl:ENSG00000083635 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1200097877 Functional Loss SNV dbSNP153 33..33 33 - - - 34919 RMVar_ID_34919 Human_SNP_ID_365362601 A-to-I Human chr8 + 60540682 60540682 60540682 TGTTACATTTTTAGTAGAGTTGGGCTTTCCCCATGTTGGCCAGGCTGGCCTGGAACTTCTGACCT TGTTACATTTTTAGTAGAGTTGGGCTTTCCCCGTGTTGGCCAGGCTGGCCTGGAACTTCTGACCT A G RAB2A Ensembl:ENSG00000104388 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs575852239 Functional Loss SNV dbSNP153 33..33 33 - - - 34920 RMVar_ID_34920 Human_SNP_ID_365369322 A-to-I Human chr8 + 60565315 60565315 60565315 GTGGCACACACCTGTAGCCCCAGCTACTTGGTAGACTGAGGCGGGAGGATTGCTTGAGCTCAAGA GTGGCACACACCTGTAGCCCCAGCTACTTGGTGGACTGAGGCGGGAGGATTGCTTGAGCTCAAGA A G RAB2A Ensembl:ENSG00000104388 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs887007543 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10130,RMVar_hsa_circ_302608,RMVar_hsa_circ_344205,RMVar_hsa_circ_252251 34921 RMVar_ID_34921 Human_SNP_ID_365375127 A-to-I Human chr8 + 60588063 60588063 60588063 AAAAGGCCGAGGCGGGAGGATTGCTTCAGCCTAGGAGTTTGAGACCAGCCTGGGCAATGTAGGGA AAAAGGCCGAGGCGGGAGGATTGCTTCAGCCTGGGAGTTTGAGACCAGCCTGGGCAATGTAGGGA A G RAB2A Ensembl:ENSG00000104388 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1363519498 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_302608,RMVar_hsa_circ_270563,RMVar_hsa_circ_60019,RMVar_hsa_circ_252252,RMVar_hsa_circ_352086,RMVar_hsa_circ_272369,RMVar_hsa_circ_252255,RMVar_hsa_circ_252256,RMVar_hsa_circ_375129 34922 RMVar_ID_34922 Human_SNP_ID_365375157 A-to-I Human chr8 + 60588156 60588156 60588156 TTTTAAAAAAGTAGCTGAACATGGTGGTACATACTTGTAGTCCCAGCTACTCCAGAGGCTGAGGT TTTTAAAAAAGTAGCTGAACATGGTGGTACATGCTTGTAGTCCCAGCTACTCCAGAGGCTGAGGT A G RAB2A Ensembl:ENSG00000104388 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1038334467 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8688930 RMVar_hsa_circ_302608,RMVar_hsa_circ_270563,RMVar_hsa_circ_60019,RMVar_hsa_circ_252252,RMVar_hsa_circ_352086,RMVar_hsa_circ_272369,RMVar_hsa_circ_252255,RMVar_hsa_circ_252256,RMVar_hsa_circ_375129 34923 RMVar_ID_34923 Human_SNP_ID_365379478 A-to-I Human chr8 + 60605029 60605029 60605029 CAGGAGCCCCTCCCTCACAGGCTCAGAGGCCTAGGAAGGAAGAATGGTTTTGTAGGTCAGGGCCA CAGGAGCCCCTCCCTCACAGGCTCAGAGGCCTGGGAAGGAAGAATGGTTTTGTAGGTCAGGGCCA A G RAB2A Ensembl:ENSG00000104388 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1399228630 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60019 34924 RMVar_ID_34924 Human_SNP_ID_365379998 A-to-I Human chr8 + 60606750 60606750 60606750 TAAAAGTCGACAAATTTTTCTAACAGTTGCCCAAGCTATACCTGGGCCTTTTTGAGCTGCAGCTA TAAAAGTCGACAAATTTTTCTAACAGTTGCCCGAGCTATACCTGGGCCTTTTTGAGCTGCAGCTA A G RAB2A Ensembl:ENSG00000104388 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs959815364 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60019 34925 RMVar_ID_34925 Human_SNP_ID_365379999 A-to-I Human chr8 + 60606750 60606750 60606750 TAAAAGTCGACAAATTTTTCTAACAGTTGCCCAAGCTATACCTGGGCCTTTTTGAGCTGCAGCTA TAAAAGTCGACAAATTTTTCTAACAGTTGCCCTAGCTATACCTGGGCCTTTTTGAGCTGCAGCTA A T RAB2A Ensembl:ENSG00000104388 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs959815364 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60019 34926 RMVar_ID_34926 Human_SNP_ID_365380010 A-to-I Human chr8 + 60606782 60606782 60606782 AAGCTATACCTGGGCCTTTTTGAGCTGCAGCTAGAGCTGGAGTGGCTGAGATACACAAGCAGTGT AAGCTATACCTGGGCCTTTTTGAGCTGCAGCTGGAGCTGGAGTGGCTGAGATACACAAGCAGTGT A G RAB2A Ensembl:ENSG00000104388 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs566433357 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60019 34927 RMVar_ID_34927 Human_SNP_ID_365380015 A-to-I Human chr8 + 60606802 60606802 60606802 TGAGCTGCAGCTAGAGCTGGAGTGGCTGAGATACACAAGCAGTGTCCTGAGGCAACACAGGTGGT TGAGCTGCAGCTAGAGCTGGAGTGGCTGAGATCCACAAGCAGTGTCCTGAGGCAACACAGGTGGT A C RAB2A Ensembl:ENSG00000104388 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1411407229 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60019 34928 RMVar_ID_34928 Human_SNP_ID_365380031 A-to-I Human chr8 + 60606855 60606855 60606855 AACACAGGTGGTGGGGCCGTGGCCTGACCTACAAAACTGTTCTTCCCTCTTAGGGCCTCCAGGCC AACACAGGTGGTGGGGCCGTGGCCTGACCTACCAAACTGTTCTTCCCTCTTAGGGCCTCCAGGCC A C RAB2A Ensembl:ENSG00000104388 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1327862909 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60019 34929 RMVar_ID_34929 Human_SNP_ID_365406837 A-to-I Human chr8 + 60713322 60713322 60713322 TTTAGTAGAGACGGGGTTTCGCCATATTGGCCAGGCTGTTCTCGACTCCTTACCTCGTGACCCGC TTTAGTAGAGACGGGGTTTCGCCATATTGGCCGGGCTGTTCTCGACTCCTTACCTCGTGACCCGC A G CHD7 Ensembl:ENSG00000171316 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs553287543 Functional Loss SNV dbSNP153 33..33 33 - - - 34930 RMVar_ID_34930 Human_SNP_ID_365415220 A-to-I Human chr8 + 60746173 60746173 60746173 CTCCTGCCTCAGCCTCCTGAGTGGCTGGGACTACAGGCGCGCACCACCGTGCCTGGCTAATTTTT CTCCTGCCTCAGCCTCCTGAGTGGCTGGGACTGCAGGCGCGCACCACCGTGCCTGGCTAATTTTT A G CHD7 Ensembl:ENSG00000171316 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs545372783 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_109 RMVar_hsa_circ_76107,RMVar_hsa_circ_95557,RMVar_hsa_circ_274526,RMVar_hsa_circ_333247,RMVar_hsa_circ_367807,RMVar_hsa_circ_118719,RMVar_hsa_circ_112433,RMVar_hsa_circ_79266,RMVar_hsa_circ_91926,RMVar_hsa_circ_77786,RMVar_hsa_circ_252260,RMVar_hsa_circ_252264,RMVar_hsa_circ_63165,RMVar_hsa_circ_73352,RMVar_hsa_circ_252266,RMVar_hsa_circ_252268,RMVar_hsa_circ_252267,RMVar_hsa_circ_252265,RMVar_hsa_circ_252262,RMVar_hsa_circ_252263,RMVar_hsa_circ_252261,RMVar_hsa_circ_252259 34931 RMVar_ID_34931 Human_SNP_ID_365418000 A-to-I Human chr8 + 60758229 60758229 60758229 ATGATCATGGCTCACTGCGTCCTCTACCTCCCAGGCTCAAGCAATCCTCCTACCTCAGCCTCCTT ATGATCATGGCTCACTGCGTCCTCTACCTCCCGGGCTCAAGCAATCCTCCTACCTCAGCCTCCTT A G CHD7 Ensembl:ENSG00000171316 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs971327526 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16447170 RMVar_hsa_circ_76107,RMVar_hsa_circ_95557,RMVar_hsa_circ_274526,RMVar_hsa_circ_333247,RMVar_hsa_circ_367807,RMVar_hsa_circ_118719,RMVar_hsa_circ_112433,RMVar_hsa_circ_79266,RMVar_hsa_circ_91926,RMVar_hsa_circ_77786,RMVar_hsa_circ_252260,RMVar_hsa_circ_252264,RMVar_hsa_circ_63165,RMVar_hsa_circ_73352,RMVar_hsa_circ_252266,RMVar_hsa_circ_252268,RMVar_hsa_circ_252267,RMVar_hsa_circ_252265,RMVar_hsa_circ_252262,RMVar_hsa_circ_252263,RMVar_hsa_circ_252261,RMVar_hsa_circ_252259,RMVar_hsa_circ_252271 34932 RMVar_ID_34932 Human_SNP_ID_365430870 A-to-I Human chr8 + 60811410 60811410 60811410 CATGCAGGTATAATTTCCTCTTCGTTCTTACAAAAAAAGAAATTGGTATACTGTTAGTACATTTT CATGCAGGTATAATTTCCTCTTCGTTCTTACAGAAAAAGAAATTGGTATACTGTTAGTACATTTT A G CHD7 Ensembl:ENSG00000171316 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs748916682 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16447971,Human_RBP_ID_21955039 RMVar_hsa_circ_76107,RMVar_hsa_circ_95557,RMVar_hsa_circ_118719,RMVar_hsa_circ_112433,RMVar_hsa_circ_79266,RMVar_hsa_circ_91926,RMVar_hsa_circ_252260,RMVar_hsa_circ_252264,RMVar_hsa_circ_63165,RMVar_hsa_circ_252262,RMVar_hsa_circ_252263,RMVar_hsa_circ_252261,RMVar_hsa_circ_41189,RMVar_hsa_circ_9487,RMVar_hsa_circ_252259,RMVar_hsa_circ_69117,RMVar_hsa_circ_265636,RMVar_hsa_circ_304494,RMVar_hsa_circ_268589,RMVar_hsa_circ_66457,RMVar_hsa_circ_252274,RMVar_hsa_circ_377134,RMVar_hsa_circ_56007 34933 RMVar_ID_34933 Human_SNP_ID_365463434 A-to-I Human chr8 + 60937889 60937889 60937889 CTCTTGTTTGACTTTCTTTGCATCATCTTTCCAGGGACTCTGTTCCTCCGGTTTCCTCTTCTTTC CTCTTGTTTGACTTTCTTTGCATCATCTTTCCGGGGACTCTGTTCCTCCGGTTTCCTCTTCTTTC A G AC022182.1 Ensembl:ENSG00000254777 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878936402 Functional Loss SNV dbSNP153 33..33 33 - - - 34934 RMVar_ID_34934 Human_SNP_ID_365463452 A-to-I Human chr8 + 60937932 60937932 60937932 TCCTCCGGTTTCCTCTTCTTTCTGACAAAGTGAGAAATATCAGTCACACAATTTGATGAGGAAGC TCCTCCGGTTTCCTCTTCTTTCTGACAAAGTGGGAAATATCAGTCACACAATTTGATGAGGAAGC A G AC022182.1 Ensembl:ENSG00000254777 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878859594 Functional Loss SNV dbSNP153 33..33 33 - - - 34935 RMVar_ID_34935 Human_SNP_ID_365463462 A-to-I Human chr8 + 60937968 60937968 60937968 ATATCAGTCACACAATTTGATGAGGAAGCACCATCTGTTGGCTTTCTACTGGCAATCAGGAGACT ATATCAGTCACACAATTTGATGAGGAAGCACCGTCTGTTGGCTTTCTACTGGCAATCAGGAGACT A G AC022182.1 Ensembl:ENSG00000254777 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879228102 Functional Loss SNV dbSNP153 33..33 33 - - - 34936 RMVar_ID_34936 Human_SNP_ID_365605934 A-to-I Human chr8 - 61514841 61514841 61514841 CCACTTAGGACCAGGCAAGGTGGTTCATGCCTATAATCCCAGAACTTTGGGTGCCCAAGGCAGGA CCACTTAGGACCAGGCAAGGTGGTTCATGCCTGTAATCCCAGAACTTTGGGTGCCCAAGGCAGGA T C ASPH Ensembl:ENSG00000198363 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1563655026 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94519,RMVar_hsa_circ_252300 34937 RMVar_ID_34937 Human_SNP_ID_365607911 A-to-I Human chr8 - 61523535 61523535 61523535 AGGCAGGCAGATCATTTGAGGTCAGGAGTTCAAGACAAGCTTGACCAACACGGTGAAACCCCATC AGGCAGGCAGATCATTTGAGGTCAGGAGTTCAGGACAAGCTTGACCAACACGGTGAAACCCCATC T C ASPH Ensembl:ENSG00000198363 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs926554023 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67952,RMVar_hsa_circ_94519,RMVar_hsa_circ_252300,RMVar_hsa_circ_288638,RMVar_hsa_circ_353926,RMVar_hsa_circ_356125,RMVar_hsa_circ_319389,RMVar_hsa_circ_126733,RMVar_hsa_circ_62714,RMVar_hsa_circ_252301,RMVar_hsa_circ_20680,RMVar_hsa_circ_252302,RMVar_hsa_circ_99077,RMVar_hsa_circ_252303 34938 RMVar_ID_34938 Human_SNP_ID_365607921 A-to-I Human chr8 - 61523583 61523583 61523583 GCTCGGTGTGGTGGCTCATGACTGTAATCCCAACACTTTGGGAGGCCGAGGCAGGCAGATCATTT GCTCGGTGTGGTGGCTCATGACTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGCAGATCATTT T C ASPH Ensembl:ENSG00000198363 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs137949011 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_3882,GWAS_ID_3883,GWAS_ID_3884,GWAS_ID_3885,GWAS_ID_3886,GWAS_ID_3887,GWAS_ID_3888,GWAS_ID_3889,GWAS_ID_3890,GWAS_ID_3891,GWAS_ID_3892,GWAS_ID_3893,GWAS_ID_3894,GWAS_ID_3895,GWAS_ID_3896,GWAS_ID_3897,GWAS_ID_3898,GWAS_ID_3899,GWAS_ID_3900,GWAS_ID_3901,GWAS_ID_3902,GWAS_ID_3903,GWAS_ID_3904,GWAS_ID_3905,GWAS_ID_3906,GWAS_ID_3907,GWAS_ID_3908,GWAS_ID_3909,GWAS_ID_3910,GWAS_ID_3911,GWAS_ID_3912,GWAS_ID_3913,GWAS_ID_3914,GWAS_ID_3915,GWAS_ID_3916,GWAS_ID_3917,GWAS_ID_3918,GWAS_ID_3919,GWAS_ID_3920,GWAS_ID_3921,GWAS_ID_3922,GWAS_ID_3923 RMVar_hsa_circ_67952,RMVar_hsa_circ_94519,RMVar_hsa_circ_252300,RMVar_hsa_circ_288638,RMVar_hsa_circ_353926,RMVar_hsa_circ_356125,RMVar_hsa_circ_319389,RMVar_hsa_circ_126733,RMVar_hsa_circ_62714,RMVar_hsa_circ_252301,RMVar_hsa_circ_20680,RMVar_hsa_circ_252302,RMVar_hsa_circ_99077,RMVar_hsa_circ_252303 34939 RMVar_ID_34939 Human_SNP_ID_365639610 A-to-I Human chr8 - 61660418 61660418 61660418 TATGTGAGTGCCCACTTTTAAACTGTTGGGTAAAGAAAAATTGGAGTCCTCTAAGGAAGTTAGTG TATGTGAGTGCCCACTTTTAAACTGTTGGGTAGAGAAAAATTGGAGTCCTCTAAGGAAGTTAGTG T C ASPH Ensembl:ENSG00000198363 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1189557472 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_702384 RMVar_hsa_circ_67952,RMVar_hsa_circ_372416,RMVar_hsa_circ_252305,RMVar_hsa_circ_18929,RMVar_hsa_circ_354845,RMVar_hsa_circ_366161,RMVar_hsa_circ_252316,RMVar_hsa_circ_37564,RMVar_hsa_circ_352039,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_39855,RMVar_hsa_circ_252325,RMVar_hsa_circ_354483,RMVar_hsa_circ_351145,RMVar_hsa_circ_272199,RMVar_hsa_circ_252328,RMVar_hsa_circ_252329 34940 RMVar_ID_34940 Human_SNP_ID_365978416 A-to-I Human chr8 - 63015371 63015371 63015371 TTGATTTATCAGTTCAGTCCAATTTATACTGGAAATATTTCTTCATTTCAGCAATGTTACATATT TTGATTTATCAGTTCAGTCCAATTTATACTGGGAATATTTCTTCATTTCAGCAATGTTACATATT T C GGH Ensembl:ENSG00000137563 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs201429647 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_702453,Human_RBP_ID_2056557,Human_RBP_ID_9227203,Human_RBP_ID_17318486,Human_RBP_ID_17433099,Human_RBP_ID_17546273 Human_Splice_Rec_981356,Human_Splice_Rec_981372,Human_Splice_Rec_981374 RMVar_hsa_circ_88655,RMVar_hsa_circ_252350 34941 RMVar_ID_34941 Human_SNP_ID_366019918 A-to-I Human chr8 + 63177887 63177887 63177887 TCAAGAAATTTTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGACACATGCTACCACGCCTG TCAAGAAATTTTCCTGCCTCAGCCTCCCAAGTGGCTGGGATTACAGACACATGCTACCACGCCTG A G YTHDF3 Ensembl:ENSG00000185728 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934739301 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63733,RMVar_hsa_circ_124231,RMVar_hsa_circ_75676,RMVar_hsa_circ_252352,RMVar_hsa_circ_277300,RMVar_hsa_circ_252353 34942 RMVar_ID_34942 Human_SNP_ID_366022045 A-to-I Human chr8 + 63184992 63184992 63184992 AAATACAAAAAATTAGCTGGGCATGGTGGCGGACGCCTGTGGTCTCAGCTACTCTGGGAGCTGAA AAATACAAAAAATTAGCTGGGCATGGTGGCGGGCGCCTGTGGTCTCAGCTACTCTGGGAGCTGAA A G YTHDF3 Ensembl:ENSG00000185728 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1180952021 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16452900,Human_RBP_ID_22625003 RMVar_hsa_circ_63733,RMVar_hsa_circ_124231,RMVar_hsa_circ_75676,RMVar_hsa_circ_252352,RMVar_hsa_circ_277300,RMVar_hsa_circ_252353 34943 RMVar_ID_34943 Human_SNP_ID_366025098 A-to-I Human chr8 + 63195991 63195991 63195991 GCCCATCTAATTTTTCTTTGTTTAGTAGAGACAGGATTTTGCCATGTCGCCCAGGTTGGTTTAGA GCCCATCTAATTTTTCTTTGTTTAGTAGAGACCGGATTTTGCCATGTCGCCCAGGTTGGTTTAGA A C YTHDF3 Ensembl:ENSG00000185728 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs938996350 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24263908 34944 RMVar_ID_34944 Human_SNP_ID_366609786 A-to-I Human chr8 - 65593353 65593353 65593353 CTGCCTTGGCCTCCAGAACTGTTGGGATTACAAGCATGAGCCAACACACCTGGCCAGCATATTTT CTGCCTTGGCCTCCAGAACTGTTGGGATTACAGGCATGAGCCAACACACCTGGCCAGCATATTTT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs907674859 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_702682 34945 RMVar_ID_34945 Human_SNP_ID_366609841 A-to-I Human chr8 - 65593594 65593594 65593594 TTTTTTTTTTTTTTGAGATAGGGTCTGTCTCTATTGCTTAGGCTGGAGTGCAGTGGCACAACCAT TTTTTTTTTTTTTTGAGATAGGGTCTGTCTCTGTTGCTTAGGCTGGAGTGCAGTGGCACAACCAT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1231064663 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16454630 34946 RMVar_ID_34946 Human_SNP_ID_366610045 A-to-I Human chr8 - 65594212 65594208 65594213 AGATTGTCATCTGCTTTCTCTTTTTTTTTTTGAGACAGAGTCTCATTCTGTCGCCCAGGCTGGAG AGATTGTCATCTGCTTTCTCTTTTTTTTTTT_____AGAGTCTCATTCTGTCGCCCAGGCTGGAG TGTCTC T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1416781596 Functional Loss DEL dbSNP153 32..36 33 - - - Human_RBP_ID_7849458 34947 RMVar_ID_34947 Human_SNP_ID_366611116 A-to-I Human chr8 - 65598403 65598403 65598403 CTGTGTTATCCCATGTTGGCCAGGCTGGTCTCAAATTCCTGACCTCAGGTGATCCACCCGTCTCG CTGTGTTATCCCATGTTGGCCAGGCTGGTCTCGAATTCCTGACCTCAGGTGATCCACCCGTCTCG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879650580 Functional Loss SNV dbSNP153 33..33 33 - - - 34948 RMVar_ID_34948 Human_SNP_ID_366631231 A-to-I Human chr8 + 65676463 65676463 65676463 TTGGCTCACTGTAGCCTCTGCCTCCCGGATTCAAGTGATTCTCCTGCCTCAGCCTCCTGAGTAGC TTGGCTCACTGTAGCCTCTGCCTCCCGGATTCGAGTGATTCTCCTGCCTCAGCCTCCTGAGTAGC A G MTFR1 Ensembl:ENSG00000066855 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs143735253 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_252368,RMVar_hsa_circ_110390,RMVar_hsa_circ_278474,RMVar_hsa_circ_344980,RMVar_hsa_circ_373150,RMVar_hsa_circ_252366,RMVar_hsa_circ_345710,RMVar_hsa_circ_120121,RMVar_hsa_circ_273174,RMVar_hsa_circ_252370,RMVar_hsa_circ_252371,RMVar_hsa_circ_252369 34949 RMVar_ID_34949 Human_SNP_ID_366634234 A-to-I Human chr8 + 65688710 65688710 65688710 TCGTGATCCGCCCGCCTTCAGGCTCCCAAAGTACTGGGATTACAGGCGTAAGCCACCGCGCCCAG TCGTGATCCGCCCGCCTTCAGGCTCCCAAAGTGCTGGGATTACAGGCGTAAGCCACCGCGCCCAG A G MTFR1 Ensembl:ENSG00000066855 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005336759 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110390,RMVar_hsa_circ_278474,RMVar_hsa_circ_344980,RMVar_hsa_circ_252366,RMVar_hsa_circ_345710,RMVar_hsa_circ_120121,RMVar_hsa_circ_273174,RMVar_hsa_circ_252370,RMVar_hsa_circ_252371,RMVar_hsa_circ_252369,RMVar_hsa_circ_65759 34950 RMVar_ID_34950 Human_SNP_ID_366634583 A-to-I Human chr8 + 65690277 65690277 65690277 GTAGTACTGGCTGGGCGTGGTGGTGCATACCTATAATCCCAGCACTTTGGGAGGCTGAGGCAGGT GTAGTACTGGCTGGGCGTGGTGGTGCATACCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGT A G MTFR1 Ensembl:ENSG00000066855 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs551796340 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110390,RMVar_hsa_circ_278474,RMVar_hsa_circ_252366,RMVar_hsa_circ_345710,RMVar_hsa_circ_120121,RMVar_hsa_circ_273174,RMVar_hsa_circ_252370,RMVar_hsa_circ_252371,RMVar_hsa_circ_252369,RMVar_hsa_circ_65759 34951 RMVar_ID_34951 Human_SNP_ID_366640334 A-to-I Human chr8 + 65713962 65713962 65713962 TGTCCGCCTCAGCCTCCCAAAGAGCTGGGATTATGGATGTGAGCCACCACACCCAGCCAACAATT TGTCCGCCTCAGCCTCCCAAAGAGCTGGGATTGTGGATGTGAGCCACCACACCCAGCCAACAATT A G MTFR1 Ensembl:ENSG00000066855 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1466136807 Functional Loss SNV dbSNP153 33..33 33 - - - 34952 RMVar_ID_34952 Human_SNP_ID_366644126 A-to-I Human chr8 - 65730283 65730283 65730283 CCAGCTACTTGGGAGGCTGAGGCAGAAGAATCACTTAAACCCGGGAGGTGGAGGTTTCGGTGAGC CCAGCTACTTGGGAGGCTGAGGCAGAAGAATCGCTTAAACCCGGGAGGTGGAGGTTTCGGTGAGC T C PDE7A Ensembl:ENSG00000205268 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs907188755 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21484,RMVar_hsa_circ_252378,RMVar_hsa_circ_302785,RMVar_hsa_circ_329933,RMVar_hsa_circ_300420,RMVar_hsa_circ_252376,RMVar_hsa_circ_252377,RMVar_hsa_circ_118338,RMVar_hsa_circ_101533,RMVar_hsa_circ_252381,RMVar_hsa_circ_39139,RMVar_hsa_circ_64154,RMVar_hsa_circ_252383 34953 RMVar_ID_34953 Human_SNP_ID_366644128 A-to-I Human chr8 - 65730290 65730290 65730290 TGTAATACCAGCTACTTGGGAGGCTGAGGCAGAAGAATCACTTAAACCCGGGAGGTGGAGGTTTC TGTAATACCAGCTACTTGGGAGGCTGAGGCAGGAGAATCACTTAAACCCGGGAGGTGGAGGTTTC T C PDE7A Ensembl:ENSG00000205268 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs986440752 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21484,RMVar_hsa_circ_252378,RMVar_hsa_circ_302785,RMVar_hsa_circ_329933,RMVar_hsa_circ_300420,RMVar_hsa_circ_252376,RMVar_hsa_circ_252377,RMVar_hsa_circ_118338,RMVar_hsa_circ_101533,RMVar_hsa_circ_252381,RMVar_hsa_circ_39139,RMVar_hsa_circ_64154,RMVar_hsa_circ_252383 34954 RMVar_ID_34954 Human_SNP_ID_366644143 A-to-I Human chr8 - 65730355 65730354 65730355 ACCAACATGGAGAAACCCTGTCTCTACTAAAAATACAAAATTAGCTGGTTGTGGTGGCGCATGCC ACCAACATGGAGAAACCCTGTCTCTACTAAAA_TACAAAATTAGCTGGTTGTGGTGGCGCATGCC AT A PDE7A Ensembl:ENSG00000205268 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1319935879 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_21484,RMVar_hsa_circ_252378,RMVar_hsa_circ_302785,RMVar_hsa_circ_329933,RMVar_hsa_circ_300420,RMVar_hsa_circ_252376,RMVar_hsa_circ_252377,RMVar_hsa_circ_118338,RMVar_hsa_circ_101533,RMVar_hsa_circ_252381,RMVar_hsa_circ_39139,RMVar_hsa_circ_64154,RMVar_hsa_circ_252383 34955 RMVar_ID_34955 Human_SNP_ID_366644144 A-to-I Human chr8 - 65730358 65730358 65730358 CTGACCAACATGGAGAAACCCTGTCTCTACTAAAAATACAAAATTAGCTGGTTGTGGTGGCGCAT CTGACCAACATGGAGAAACCCTGTCTCTACTACAAATACAAAATTAGCTGGTTGTGGTGGCGCAT T G PDE7A Ensembl:ENSG00000205268 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs987452845 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21484,RMVar_hsa_circ_252378,RMVar_hsa_circ_302785,RMVar_hsa_circ_329933,RMVar_hsa_circ_300420,RMVar_hsa_circ_252376,RMVar_hsa_circ_252377,RMVar_hsa_circ_118338,RMVar_hsa_circ_101533,RMVar_hsa_circ_252381,RMVar_hsa_circ_39139,RMVar_hsa_circ_64154,RMVar_hsa_circ_252383 34956 RMVar_ID_34956 Human_SNP_ID_366644152 A-to-I Human chr8 - 65730393 65730393 65730393 GGTGGATCACCTGAGGTTGGGAGTTCGAGACCAGCCTGACCAACATGGAGAAACCCTGTCTCTAC GGTGGATCACCTGAGGTTGGGAGTTCGAGACCTGCCTGACCAACATGGAGAAACCCTGTCTCTAC T A PDE7A Ensembl:ENSG00000205268 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs562981170 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21484,RMVar_hsa_circ_252378,RMVar_hsa_circ_302785,RMVar_hsa_circ_329933,RMVar_hsa_circ_300420,RMVar_hsa_circ_252376,RMVar_hsa_circ_252377,RMVar_hsa_circ_118338,RMVar_hsa_circ_101533,RMVar_hsa_circ_252381,RMVar_hsa_circ_39139,RMVar_hsa_circ_64154,RMVar_hsa_circ_252383 34957 RMVar_ID_34957 Human_SNP_ID_366644153 A-to-I Human chr8 - 65730393 65730393 65730393 GGTGGATCACCTGAGGTTGGGAGTTCGAGACCAGCCTGACCAACATGGAGAAACCCTGTCTCTAC GGTGGATCACCTGAGGTTGGGAGTTCGAGACCGGCCTGACCAACATGGAGAAACCCTGTCTCTAC T C PDE7A Ensembl:ENSG00000205268 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs562981170 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21484,RMVar_hsa_circ_252378,RMVar_hsa_circ_302785,RMVar_hsa_circ_329933,RMVar_hsa_circ_300420,RMVar_hsa_circ_252376,RMVar_hsa_circ_252377,RMVar_hsa_circ_118338,RMVar_hsa_circ_101533,RMVar_hsa_circ_252381,RMVar_hsa_circ_39139,RMVar_hsa_circ_64154,RMVar_hsa_circ_252383 34958 RMVar_ID_34958 Human_SNP_ID_366644176 A-to-I Human chr8 - 65730459 65730459 65730459 AAGAAGTGTGCTGGCTGGGCTTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGC AAGAAGTGTGCTGGCTGGGCTTGGTGGCTCACTCCTGTAATCCCAGCACTTTGGGAGGCTGAGGC T A PDE7A Ensembl:ENSG00000205268 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1001960272 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21484,RMVar_hsa_circ_252378,RMVar_hsa_circ_302785,RMVar_hsa_circ_329933,RMVar_hsa_circ_300420,RMVar_hsa_circ_252376,RMVar_hsa_circ_252377,RMVar_hsa_circ_118338,RMVar_hsa_circ_101533,RMVar_hsa_circ_252381,RMVar_hsa_circ_39139,RMVar_hsa_circ_64154,RMVar_hsa_circ_252383 34959 RMVar_ID_34959 Human_SNP_ID_366644177 A-to-I Human chr8 - 65730459 65730459 65730459 AAGAAGTGTGCTGGCTGGGCTTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGC AAGAAGTGTGCTGGCTGGGCTTGGTGGCTCACCCCTGTAATCCCAGCACTTTGGGAGGCTGAGGC T G PDE7A Ensembl:ENSG00000205268 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1001960272 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21484,RMVar_hsa_circ_252378,RMVar_hsa_circ_302785,RMVar_hsa_circ_329933,RMVar_hsa_circ_300420,RMVar_hsa_circ_252376,RMVar_hsa_circ_252377,RMVar_hsa_circ_118338,RMVar_hsa_circ_101533,RMVar_hsa_circ_252381,RMVar_hsa_circ_39139,RMVar_hsa_circ_64154,RMVar_hsa_circ_252383 34960 RMVar_ID_34960 Human_SNP_ID_366644240 A-to-I Human chr8 - 65730723 65730723 65730723 GGGTTTTGCCATGATGGCCAGGCTAGTCTCGAACTCCTGACTTCAAGTGATCTGCCTGCCTTGGC GGGTTTTGCCATGATGGCCAGGCTAGTCTCGACCTCCTGACTTCAAGTGATCTGCCTGCCTTGGC T G PDE7A Ensembl:ENSG00000205268 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1366094743 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21484,RMVar_hsa_circ_252378,RMVar_hsa_circ_302785,RMVar_hsa_circ_329933,RMVar_hsa_circ_300420,RMVar_hsa_circ_252376,RMVar_hsa_circ_252377,RMVar_hsa_circ_118338,RMVar_hsa_circ_101533,RMVar_hsa_circ_252381,RMVar_hsa_circ_39139,RMVar_hsa_circ_64154,RMVar_hsa_circ_252383 34961 RMVar_ID_34961 Human_SNP_ID_366644266 A-to-I Human chr8 - 65730840 65730840 65730840 TAGCTCACTGCAACCTCCACCTCCTGGGTTCAAGCGATTCTCTTGTCTCAGCCTCCCAAGTAGCT TAGCTCACTGCAACCTCCACCTCCTGGGTTCAGGCGATTCTCTTGTCTCAGCCTCCCAAGTAGCT T C PDE7A Ensembl:ENSG00000205268 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1303239454 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21484,RMVar_hsa_circ_252378,RMVar_hsa_circ_302785,RMVar_hsa_circ_329933,RMVar_hsa_circ_300420,RMVar_hsa_circ_252376,RMVar_hsa_circ_252377,RMVar_hsa_circ_118338,RMVar_hsa_circ_101533,RMVar_hsa_circ_252381,RMVar_hsa_circ_39139,RMVar_hsa_circ_64154,RMVar_hsa_circ_252383 34962 RMVar_ID_34962 Human_SNP_ID_366645394 A-to-I Human chr8 - 65735754 65735754 65735754 GAGCATGATGGCAGGTGCCTGTAATCCCAGCTACTCGGGTGGCTGAGGCGGGAGGATCACTTGAA GAGCATGATGGCAGGTGCCTGTAATCCCAGCTGCTCGGGTGGCTGAGGCGGGAGGATCACTTGAA T C PDE7A Ensembl:ENSG00000205268 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1451507238 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21484,RMVar_hsa_circ_252378,RMVar_hsa_circ_302785,RMVar_hsa_circ_329933,RMVar_hsa_circ_300420,RMVar_hsa_circ_252376,RMVar_hsa_circ_252377,RMVar_hsa_circ_118338,RMVar_hsa_circ_101533,RMVar_hsa_circ_252381,RMVar_hsa_circ_252386,RMVar_hsa_circ_39139,RMVar_hsa_circ_64154,RMVar_hsa_circ_252383,RMVar_hsa_circ_299011,RMVar_hsa_circ_308856,RMVar_hsa_circ_309710,RMVar_hsa_circ_271443,RMVar_hsa_circ_252384,RMVar_hsa_circ_252385 34963 RMVar_ID_34963 Human_SNP_ID_366665247 A-to-I Human chr8 - 65820239 65820239 65820239 GGCATGTGCCACCATGTCCCGCTAATTATTGTATTTTTAGTAGAGACAGGATTTTGCCATGTTGG GGCATGTGCCACCATGTCCCGCTAATTATTGTGTTTTTAGTAGAGACAGGATTTTGCCATGTTGG T C PDE7A Ensembl:ENSG00000205268 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs563048779 Functional Loss SNV dbSNP153 33..33 33 - - - 34964 RMVar_ID_34964 Human_SNP_ID_366818520 A-to-I Human chr8 + 66454938 66454938 66454938 CGGGGTTTCACCATGTTGGCCTGGCTGGTCTCAAACTCCTGACCTTAGTTATCCACCCGCCTCCA CGGGGTTTCACCATGTTGGCCTGGCTGGTCTCGAACTCCTGACCTTAGTTATCCACCCGCCTCCA A G AC009879.3,ADHFE1 Ensembl:ENSG00000285791,Ensembl:ENSG00000147576 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1015331973 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73979,RMVar_hsa_circ_74777 34965 RMVar_ID_34965 Human_SNP_ID_366860727 A-to-I Human chr8 - 66631607 66631607 66631607 CAGTCAAGCCTACTGCTTGCAATTAAGATATCAATCTGAAATGCATCTGTAATTCCTGGCCACAG CAGTCAAGCCTACTGCTTGCAATTAAGATATCTATCTGAAATGCATCTGTAATTCCTGGCCACAG T A VCPIP1 Ensembl:ENSG00000175073 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs910449101 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17546386,Human_RBP_ID_22410347 34966 RMVar_ID_34966 Human_SNP_ID_366864831 A-to-I Human chr8 - 66648734 66648734 66648734 TGGCCAACATGGTAAAACCTCATCTCTTCAAAAAATACAAAAAAATTAGCCGGGTGTGGTGGTGC TGGCCAACATGGTAAAACCTCATCTCTTCAAAGAATACAAAAAAATTAGCCGGGTGTGGTGGTGC T C VCPIP1 Ensembl:ENSG00000175073 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1207281144 Functional Loss SNV dbSNP153 33..33 33 - - - 34967 RMVar_ID_34967 Human_SNP_ID_366864834 A-to-I Human chr8 - 66648745 66648745 66648746 TGAGACCAGCCTGGCCAACATGGTAAAACCTCATCTCTTCAAAAAATACAAAAAAATTAGCCGGG TGAGACCAGCCTGGCCAACATGGTAAAACCTTGTCTCTTCAAAAAATACAAAAAAATTAGCCGGG TG CA VCPIP1 Ensembl:ENSG00000175073 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs71561292 Functional Loss MNV dbSNP153 32..33 33 - - - 34968 RMVar_ID_34968 Human_SNP_ID_366864871 A-to-I Human chr8 - 66648943 66648943 66648943 GTTGCCTAGGCTTGTCTTGAATTCCTGAGCTCAGGTGATCTTCCTGCATCGGCCTCCCAAAGTGT GTTGCCTAGGCTTGTCTTGAATTCCTGAGCTCGGGTGATCTTCCTGCATCGGCCTCCCAAAGTGT T C VCPIP1 Ensembl:ENSG00000175073 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1292108028 Functional Loss SNV dbSNP153 33..33 33 - - - 34969 RMVar_ID_34969 Human_SNP_ID_366871159 A-to-I Human chr8 + 66674130 66674130 66674130 GCAACTTGCCTGTCTCAGCTTCCCAAGTAGCTAGGACTACAGGCGCCTGCCACCACACCCGGCTA GCAACTTGCCTGTCTCAGCTTCCCAAGTAGCTGGGACTACAGGCGCCTGCCACCACACCCGGCTA A G C8orf44,C8orf44-SGK3 Ensembl:ENSG00000288596,Ensembl:ENSG00000288602 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1460089556 Functional Loss SNV dbSNP153 33..33 33 - - - 34970 RMVar_ID_34970 Human_SNP_ID_366871370 A-to-I Human chr8 + 66675259 66675259 66675259 CACTTTGGGAAGCTTAGACTGGAGGATTACCTAAGGCCAGGAGTTCAAGAACAACTTGGTCAACC CACTTTGGGAAGCTTAGACTGGAGGATTACCTGAGGCCAGGAGTTCAAGAACAACTTGGTCAACC A G C8orf44,C8orf44-SGK3 Ensembl:ENSG00000288596,Ensembl:ENSG00000288602 Protein coding,Protein coding intron,intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs998701481 Functional Loss SNV dbSNP153 33..33 33 - - - 34971 RMVar_ID_34971 Human_SNP_ID_366871758 A-to-I Human chr8 + 66677111 66677111 66677111 TCAAGCGATTCTCCTACCTCAGCCTCCCAAGTAGCTGGAATTACAGGCACCTGCTACAACACCCG TCAAGCGATTCTCCTACCTCAGCCTCCCAAGTCGCTGGAATTACAGGCACCTGCTACAACACCCG A C C8orf44,C8orf44-SGK3 Ensembl:ENSG00000288596,Ensembl:ENSG00000288602 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1177794967 Functional Loss SNV dbSNP153 33..33 33 - - - 34972 RMVar_ID_34972 Human_SNP_ID_366871774 A-to-I Human chr8 + 66677178 66677178 66677178 TAATTTTTGTAGTTTTTGTAGAGACGAGTTTCACCATGTTGACCAGGCTGGTCTCAAACTCTTGA TAATTTTTGTAGTTTTTGTAGAGACGAGTTTCCCCATGTTGACCAGGCTGGTCTCAAACTCTTGA A C C8orf44,C8orf44-SGK3 Ensembl:ENSG00000288596,Ensembl:ENSG00000288602 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1051854246 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16458222 34973 RMVar_ID_34973 Human_SNP_ID_366871776 A-to-I Human chr8 + 66677190 66677190 66677190 TTTTTGTAGAGACGAGTTTCACCATGTTGACCAGGCTGGTCTCAAACTCTTGACGTCAAATGATC TTTTTGTAGAGACGAGTTTCACCATGTTGACCCGGCTGGTCTCAAACTCTTGACGTCAAATGATC A C C8orf44,C8orf44-SGK3 Ensembl:ENSG00000288596,Ensembl:ENSG00000288602 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560705996 Functional Loss SNV dbSNP153 33..33 33 - - - 34974 RMVar_ID_34974 Human_SNP_ID_366871779 A-to-I Human chr8 + 66677201 66677201 66677201 ACGAGTTTCACCATGTTGACCAGGCTGGTCTCAAACTCTTGACGTCAAATGATCCACCTGCCTCA ACGAGTTTCACCATGTTGACCAGGCTGGTCTCGAACTCTTGACGTCAAATGATCCACCTGCCTCA A G C8orf44,C8orf44-SGK3 Ensembl:ENSG00000288596,Ensembl:ENSG00000288602 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1160143516 Functional Loss SNV dbSNP153 33..33 33 - - - 34975 RMVar_ID_34975 Human_SNP_ID_366872009 A-to-I Human chr8 + 66677953 66677953 66677953 CCCCATCTTTACTAAAAATACGAAAATTAGCCAGGTGCGGTGGTGCATACCTGTAATCTCAGCTA CCCCATCTTTACTAAAAATACGAAAATTAGCCGGGTGCGGTGGTGCATACCTGTAATCTCAGCTA A G C8orf44,C8orf44-SGK3 Ensembl:ENSG00000288596,Ensembl:ENSG00000288602 Protein coding,Protein coding CDS,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs568554290 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_982683,Human_Splice_Rec_982691,Human_Splice_Rec_982697,Human_Splice_Rec_982703 34976 RMVar_ID_34976 Human_SNP_ID_366872010 A-to-I Human chr8 + 66677953 66677953 66677953 CCCCATCTTTACTAAAAATACGAAAATTAGCCAGGTGCGGTGGTGCATACCTGTAATCTCAGCTA CCCCATCTTTACTAAAAATACGAAAATTAGCCTGGTGCGGTGGTGCATACCTGTAATCTCAGCTA A T C8orf44,C8orf44-SGK3 Ensembl:ENSG00000288596,Ensembl:ENSG00000288602 Protein coding,Protein coding CDS,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs568554290 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_982683,Human_Splice_Rec_982691,Human_Splice_Rec_982697,Human_Splice_Rec_982703 34977 RMVar_ID_34977 Human_SNP_ID_366872825 A-to-I Human chr8 + 66681056 66681055 66681056 GTGGTGCATGCCTGTAGTCCTAGCTACTCGGGAAGCTGAGGCAAGAGGATAGCCTGAGCCCAGGG GTGGTGCATGCCTGTAGTCCTAGCTACTCGGG_AGCTGAGGCAAGAGGATAGCCTGAGCCCAGGG GA G C8orf44,C8orf44-SGK3 Ensembl:ENSG00000288596,Ensembl:ENSG00000288602 Protein coding,Protein coding 3'UTR,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1271772465 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_38591 34978 RMVar_ID_34978 Human_SNP_ID_366875693 A-to-I Human chr8 + 66693512 66693512 66693512 CTACTGCCTCAGCCTCCTGAGTGGCTGGTATTACAGGCATGTGCCACCACGCCCGGCTAATTTTG CTACTGCCTCAGCCTCCTGAGTGGCTGGTATTGCAGGCATGTGCCACCACGCCCGGCTAATTTTG A G C8orf44-SGK3 Ensembl:ENSG00000288602 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1216956793 Functional Loss SNV dbSNP153 33..33 33 - - - 34979 RMVar_ID_34979 Human_SNP_ID_366944743 A-to-I Human chr8 - 66985951 66985948 66985951 GCAGTGACGGAAGCAGAAAACGAAAGCTAAAGAAGGTGTTTGGTGATGACTCTTGAGCTCTCCAA GCAGTGACGGAAGCAGAAAACGAAAGCTAAAG___GTGTTTGGTGATGACTCTTGAGCTCTCCAA CCTT C PPP1R42,AC110998.1 Ensembl:ENSG00000178125,Ensembl:ENSG00000253223 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264118727 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_252434,RMVar_hsa_circ_328464 34980 RMVar_ID_34980 Human_SNP_ID_366957653 A-to-I Human chr8 - 67044667 67044667 67044667 TCCACCCAGGAGGTGGAGATTGCAGTGAGCCAAGATGGCGCCATTGCACTCCAGCCTGGCCAACA TCCACCCAGGAGGTGGAGATTGCAGTGAGCCAGGATGGCGCCATTGCACTCCAGCCTGGCCAACA T C PPP1R42,COPS5 Ensembl:ENSG00000178125,Ensembl:ENSG00000121022 Protein coding,Protein coding intron,intron GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line - 24183664,31158229 RNA-Seq:(High) rs1284970096 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99053,RMVar_hsa_circ_252437 34981 RMVar_ID_34981 Human_SNP_ID_366957691 A-to-I Human chr8 - 67044879 67044879 67044879 ATTTGAATTTTAGGCCGGGCACAGTGGTTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGC ATTTGAATTTTAGGCCGGGCACAGTGGTTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGC T C PPP1R42,COPS5 Ensembl:ENSG00000178125,Ensembl:ENSG00000121022 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs895982284 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99053,RMVar_hsa_circ_252437 34982 RMVar_ID_34982 Human_SNP_ID_366957778 A-to-I Human chr8 - 67045334 67045334 67045334 TTCTCCCGCCTCAGCCTCCCAAGTAACTGGGAATATAGGCACCTGCCATCATGCCTGACTAATTT TTCTCCCGCCTCAGCCTCCCAAGTAACTGGGATTATAGGCACCTGCCATCATGCCTGACTAATTT T A PPP1R42,COPS5 Ensembl:ENSG00000178125,Ensembl:ENSG00000121022 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1433914502 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99053,RMVar_hsa_circ_252437 34983 RMVar_ID_34983 Human_SNP_ID_366957782 A-to-I Human chr8 - 67045354 67045354 67045354 CGCCTACCGGGTTCAAGCGATTCTCCCGCCTCAGCCTCCCAAGTAACTGGGAATATAGGCACCTG CGCCTACCGGGTTCAAGCGATTCTCCCGCCTCGGCCTCCCAAGTAACTGGGAATATAGGCACCTG T C PPP1R42,COPS5 Ensembl:ENSG00000178125,Ensembl:ENSG00000121022 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1366770157 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99053,RMVar_hsa_circ_252437 34984 RMVar_ID_34984 Human_SNP_ID_366982391 A-to-I Human chr8 + 67150435 67150421 67150436 ATGTTGTTTTTTTTTTTGTGAGATGGAGTCTCACTTTGTTATCCCAGGCTGGAGTGCAGTGGCAT ATGTTGTTTTTTTTTTTGT_______________TTTGTTATCCCAGGCTGGAGTGCAGTGGCAT TGAGATGGAGTCTCAC T CSPP1 Ensembl:ENSG00000104218 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1554599930 Functional Loss DEL dbSNP153 20..34 33 - - - RMVar_hsa_circ_7486,RMVar_hsa_circ_365717,RMVar_hsa_circ_114154,RMVar_hsa_circ_30904,RMVar_hsa_circ_252447,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_292862,RMVar_hsa_circ_125750,RMVar_hsa_circ_60609,RMVar_hsa_circ_252480,RMVar_hsa_circ_252481,RMVar_hsa_circ_45641,RMVar_hsa_circ_367747,RMVar_hsa_circ_62091,RMVar_hsa_circ_252494,RMVar_hsa_circ_75464,RMVar_hsa_circ_366704,RMVar_hsa_circ_358910,RMVar_hsa_circ_14549,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_342273,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_252503,RMVar_hsa_circ_9577,RMVar_hsa_circ_58455,RMVar_hsa_circ_252505,RMVar_hsa_circ_252506,RMVar_hsa_circ_252504 34985 RMVar_ID_34985 Human_SNP_ID_366990916 A-to-I Human chr8 - 67184672 67184672 67184672 TCATGCAGGCTGGAGTGCAGTGGCACGATTTCAGCTCACTGTAACCTCCACCTCCTGGTTCAAGT TCATGCAGGCTGGAGTGCAGTGGCACGATTTCGGCTCACTGTAACCTCCACCTCCTGGTTCAAGT T C ARFGEF1 Ensembl:ENSG00000066777 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1162502044 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_252514,RMVar_hsa_circ_90951 34986 RMVar_ID_34986 Human_SNP_ID_366996584 A-to-I Human chr8 - 67205235 67205235 67205235 GGAGGCAGACAATTGCCCAAAGGGAGCTGCCTACTAGGCAGTCTTGGGGCAGTGGCTCCAATGCT GGAGGCAGACAATTGCCCAAAGGGAGCTGCCTGCTAGGCAGTCTTGGGGCAGTGGCTCCAATGCT T C ARFGEF1 Ensembl:ENSG00000066777 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs981672924 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2655,RMVar_hsa_circ_252514,RMVar_hsa_circ_90951,RMVar_hsa_circ_377342,RMVar_hsa_circ_267266,RMVar_hsa_circ_268101,RMVar_hsa_circ_252521,RMVar_hsa_circ_252520,RMVar_hsa_circ_125179,RMVar_hsa_circ_281436 34987 RMVar_ID_34987 Human_SNP_ID_366996596 A-to-I Human chr8 - 67205294 67205294 67205294 ACCACATGGCCACACCTCCATCCCAGATTCTCAGGGCAGCTTTGGCAGGAAGCTTTCCAGGAGGC ACCACATGGCCACACCTCCATCCCAGATTCTCCGGGCAGCTTTGGCAGGAAGCTTTCCAGGAGGC T G ARFGEF1 Ensembl:ENSG00000066777 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs891211906 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2655,RMVar_hsa_circ_252514,RMVar_hsa_circ_90951,RMVar_hsa_circ_377342,RMVar_hsa_circ_267266,RMVar_hsa_circ_268101,RMVar_hsa_circ_252521,RMVar_hsa_circ_252520,RMVar_hsa_circ_125179,RMVar_hsa_circ_281436 34988 RMVar_ID_34988 Human_SNP_ID_367006775 A-to-I Human chr8 - 67244069 67244069 67244069 TCTGGCTGATTTTTTGTATTTTTAGTAGAGACAGGGTTTTGTCATGTTGGCCAGGCTGGTCTCAA TCTGGCTGATTTTTTGTATTTTTAGTAGAGACGGGGTTTTGTCATGTTGGCCAGGCTGGTCTCAA T C ARFGEF1 Ensembl:ENSG00000066777 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1312856534 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9779,RMVar_hsa_circ_20067,RMVar_hsa_circ_252520,RMVar_hsa_circ_125179,RMVar_hsa_circ_324843,RMVar_hsa_circ_52814,RMVar_hsa_circ_14848,RMVar_hsa_circ_252524,RMVar_hsa_circ_252525,RMVar_hsa_circ_68438,RMVar_hsa_circ_362999,RMVar_hsa_circ_252526,RMVar_hsa_circ_348917,RMVar_hsa_circ_124015,RMVar_hsa_circ_8586,RMVar_hsa_circ_47838,RMVar_hsa_circ_29234,RMVar_hsa_circ_252527,RMVar_hsa_circ_252528,RMVar_hsa_circ_343163,RMVar_hsa_circ_252534,RMVar_hsa_circ_96099,RMVar_hsa_circ_12942,RMVar_hsa_circ_112112,RMVar_hsa_circ_306133,RMVar_hsa_circ_252535,RMVar_hsa_circ_252536,RMVar_hsa_circ_252537,RMVar_hsa_circ_72149,RMVar_hsa_circ_266441,RMVar_hsa_circ_332149,RMVar_hsa_circ_339839,RMVar_hsa_circ_366940,RMVar_hsa_circ_338960,RMVar_hsa_circ_18420,RMVar_hsa_circ_322855,RMVar_hsa_circ_252539,RMVar_hsa_circ_252540,RMVar_hsa_circ_252538,RMVar_hsa_circ_328115,RMVar_hsa_circ_47645,RMVar_hsa_circ_316831,RMVar_hsa_circ_23785,RMVar_hsa_circ_252543,RMVar_hsa_circ_4855,RMVar_hsa_circ_252542 34989 RMVar_ID_34989 Human_SNP_ID_367006776 A-to-I Human chr8 - 67244075 67244075 67244075 ACCATGTCTGGCTGATTTTTTGTATTTTTAGTAGAGACAGGGTTTTGTCATGTTGGCCAGGCTGG ACCATGTCTGGCTGATTTTTTGTATTTTTAGTGGAGACAGGGTTTTGTCATGTTGGCCAGGCTGG T C ARFGEF1 Ensembl:ENSG00000066777 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs911627969 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26180582 RMVar_hsa_circ_9779,RMVar_hsa_circ_20067,RMVar_hsa_circ_252520,RMVar_hsa_circ_125179,RMVar_hsa_circ_324843,RMVar_hsa_circ_52814,RMVar_hsa_circ_14848,RMVar_hsa_circ_252524,RMVar_hsa_circ_252525,RMVar_hsa_circ_68438,RMVar_hsa_circ_362999,RMVar_hsa_circ_252526,RMVar_hsa_circ_348917,RMVar_hsa_circ_124015,RMVar_hsa_circ_8586,RMVar_hsa_circ_47838,RMVar_hsa_circ_29234,RMVar_hsa_circ_252527,RMVar_hsa_circ_252528,RMVar_hsa_circ_343163,RMVar_hsa_circ_252534,RMVar_hsa_circ_96099,RMVar_hsa_circ_12942,RMVar_hsa_circ_112112,RMVar_hsa_circ_306133,RMVar_hsa_circ_252535,RMVar_hsa_circ_252536,RMVar_hsa_circ_252537,RMVar_hsa_circ_72149,RMVar_hsa_circ_266441,RMVar_hsa_circ_332149,RMVar_hsa_circ_339839,RMVar_hsa_circ_366940,RMVar_hsa_circ_338960,RMVar_hsa_circ_18420,RMVar_hsa_circ_322855,RMVar_hsa_circ_252539,RMVar_hsa_circ_252540,RMVar_hsa_circ_252538,RMVar_hsa_circ_328115,RMVar_hsa_circ_47645,RMVar_hsa_circ_316831,RMVar_hsa_circ_23785,RMVar_hsa_circ_252543,RMVar_hsa_circ_4855,RMVar_hsa_circ_252542 34990 RMVar_ID_34990 Human_SNP_ID_367021517 A-to-I Human chr8 - 67303548 67303548 67303548 CACCAGCACGCCTGGCTAATTTTTGTGTTTTTAGTAGAGACGATGTTTCACCACGTTGGCCAGAC CACCAGCACGCCTGGCTAATTTTTGTGTTTTTGGTAGAGACGATGTTTCACCACGTTGGCCAGAC T C ARFGEF1 Ensembl:ENSG00000066777 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs542824019 Functional Loss SNV dbSNP153 33..33 33 - - - 34991 RMVar_ID_34991 Human_SNP_ID_367029297 A-to-I Human chr8 - 67333173 67333173 67333173 AAAATTAGCTGGCTGTGGTGGTGCGTGCCTGTAGTCCAGCTGCTCGGGCGGCTGAGGCAGGAGAA AAAATTAGCTGGCTGTGGTGGTGCGTGCCTGTCGTCCAGCTGCTCGGGCGGCTGAGGCAGGAGAA T G ARFGEF1 Ensembl:ENSG00000066777 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1316715400 Functional Loss SNV dbSNP153 33..33 33 - - - 34992 RMVar_ID_34992 Human_SNP_ID_367468454 A-to-I Human chr8 + 69129969 69129969 69129969 ACATTGCGGAAAAGGCTGACCGCAAATACGAGAAGGTAGCTCGTAAGCTGGTCATCCTGGAGGGT ACATTGCGGAAAAGGCTGACCGCAAATACGAGCAGGTAGCTCGTAAGCTGGTCATCCTGGAGGGT A C AF201337.1 Ensembl:ENSG00000254332 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs575790564 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17715133,Human_RBP_ID_18125508 34993 RMVar_ID_34993 Human_SNP_ID_367468455 A-to-I Human chr8 + 69129969 69129969 69129969 ACATTGCGGAAAAGGCTGACCGCAAATACGAGAAGGTAGCTCGTAAGCTGGTCATCCTGGAGGGT ACATTGCGGAAAAGGCTGACCGCAAATACGAGGAGGTAGCTCGTAAGCTGGTCATCCTGGAGGGT A G AF201337.1 Ensembl:ENSG00000254332 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs575790564 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17715133,Human_RBP_ID_18125508 34994 RMVar_ID_34994 Human_SNP_ID_367606874 A-to-I Human chr8 - 69690301 69690301 69690301 GAATGTCAAATTGAAGAAATTCAATGAAGCACAGGTAAATGGTGGGAGTAACTATGACTCTCTTA GAATGTCAAATTGAAGAAATTCAATGAAGCACGGGTAAATGGTGGGAGTAACTATGACTCTCTTA T C SLCO5A1 Ensembl:ENSG00000137571 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs7844100 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1117766 RMVar_hsa_circ_333705,RMVar_hsa_circ_252622,RMVar_hsa_circ_252621,RMVar_hsa_circ_337620,RMVar_hsa_circ_288153,RMVar_hsa_circ_285450,RMVar_hsa_circ_252625,RMVar_hsa_circ_252627,RMVar_hsa_circ_252626,RMVar_hsa_circ_307345,RMVar_hsa_circ_252624,RMVar_hsa_circ_265698,RMVar_hsa_circ_32484,RMVar_hsa_circ_252629,RMVar_hsa_circ_318916,RMVar_hsa_circ_252630 34995 RMVar_ID_34995 Human_SNP_ID_367633861 A-to-I Human chr8 - 69804509 69804509 69804509 GAGTTTGAGAACAGCCTGGGCAACATGGTGAAACCCCGCCTCTACTAAAAATATAAAAATTAGTC GAGTTTGAGAACAGCCTGGGCAACATGGTGAACCCCCGCCTCTACTAAAAATATAAAAATTAGTC T G SLCO5A1 Ensembl:ENSG00000137571 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1012812917 Functional Loss SNV dbSNP153 33..33 33 - - - 34996 RMVar_ID_34996 Human_SNP_ID_367716561 A-to-I Human chr8 - 70118794 70118794 70118794 GTCCCAGCTACTCGGGAGGCTGAGATAGGAGAATTGCTTGAACCTGGGAGGCGGAAGTTGTAGTG GTCCCAGCTACTCGGGAGGCTGAGATAGGAGAGTTGCTTGAACCTGGGAGGCGGAAGTTGTAGTG T C NCOA2 Ensembl:ENSG00000140396 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041075029 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111457,RMVar_hsa_circ_252638 34997 RMVar_ID_34997 Human_SNP_ID_367716585 A-to-I Human chr8 - 70118914 70118913 70118915 GGAGGCTGAGGCGGATGGATCACCTGAGGTCAAGAGTTTGAGACTAGCCTGGCTAACATGGTGAA GGAGGCTGAGGCGGATGGATCACCTGAGGTC__GAGTTTGAGACTAGCCTGGCTAACATGGTGAA CTT C NCOA2 Ensembl:ENSG00000140396 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1023482380 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_111457,RMVar_hsa_circ_252638 34998 RMVar_ID_34998 Human_SNP_ID_367716586 A-to-I Human chr8 - 70118914 70118914 70118914 GGAGGCTGAGGCGGATGGATCACCTGAGGTCAAGAGTTTGAGACTAGCCTGGCTAACATGGTGAA GGAGGCTGAGGCGGATGGATCACCTGAGGTCAGGAGTTTGAGACTAGCCTGGCTAACATGGTGAA T C NCOA2 Ensembl:ENSG00000140396 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs969781163 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111457,RMVar_hsa_circ_252638 34999 RMVar_ID_34999 Human_SNP_ID_367722570 A-to-I Human chr8 - 70143123 70143123 70143123 CAACATGGTGAAACCTCATCTCCACTAAAAATACAAAAATTAAATGGGCGTGGTGGCGTGCACCT CAACATGGTGAAACCTCATCTCCACTAAAAATGCAAAAATTAAATGGGCGTGGTGGCGTGCACCT T C NCOA2 Ensembl:ENSG00000140396 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs765729839 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103301,RMVar_hsa_circ_314449,RMVar_hsa_circ_111457,RMVar_hsa_circ_355630,RMVar_hsa_circ_252638,RMVar_hsa_circ_281283,RMVar_hsa_circ_252639,RMVar_hsa_circ_252640,RMVar_hsa_circ_294670,RMVar_hsa_circ_345411,RMVar_hsa_circ_298767,RMVar_hsa_circ_252642,RMVar_hsa_circ_252644,RMVar_hsa_circ_252645,RMVar_hsa_circ_252643,RMVar_hsa_circ_118323,RMVar_hsa_circ_252647,RMVar_hsa_circ_377101,RMVar_hsa_circ_376095,RMVar_hsa_circ_252646,RMVar_hsa_circ_68083,RMVar_hsa_circ_41127,RMVar_hsa_circ_88254,RMVar_hsa_circ_252649,RMVar_hsa_circ_106213,RMVar_hsa_circ_361237,RMVar_hsa_circ_74648,RMVar_hsa_circ_83570,RMVar_hsa_circ_252650,RMVar_hsa_circ_252651,RMVar_hsa_circ_252652,RMVar_hsa_circ_375973,RMVar_hsa_circ_297751,RMVar_hsa_circ_74481,RMVar_hsa_circ_329751,RMVar_hsa_circ_252653,RMVar_hsa_circ_252654,RMVar_hsa_circ_362557,RMVar_hsa_circ_307273,RMVar_hsa_circ_324474,RMVar_hsa_circ_285240,RMVar_hsa_circ_333099,RMVar_hsa_circ_252656,RMVar_hsa_circ_46154,RMVar_hsa_circ_252657,RMVar_hsa_circ_252655 35000 RMVar_ID_35000 Human_SNP_ID_367735739 A-to-I Human chr8 - 70197922 70197922 70197922 TGGTGGTGTGTGCCTGTAGTTCTAGCTACTCAAGAGGCTGAGCTGGGAGGATCACTTGAGCCAAT TGGTGGTGTGTGCCTGTAGTTCTAGCTACTCAGGAGGCTGAGCTGGGAGGATCACTTGAGCCAAT T C NCOA2 Ensembl:ENSG00000140396 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs995673879 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103301,RMVar_hsa_circ_252645,RMVar_hsa_circ_68083,RMVar_hsa_circ_106213,RMVar_hsa_circ_74648,RMVar_hsa_circ_252651,RMVar_hsa_circ_74481,RMVar_hsa_circ_362557,RMVar_hsa_circ_53916,RMVar_hsa_circ_2394,RMVar_hsa_circ_284058,RMVar_hsa_circ_72919,RMVar_hsa_circ_252664,RMVar_hsa_circ_252665,RMVar_hsa_circ_318959,RMVar_hsa_circ_355301 35001 RMVar_ID_35001 Human_SNP_ID_367735741 A-to-I Human chr8 - 70197937 70197937 70197937 AAAATTAAATGGGCATGGTGGTGTGTGCCTGTAGTTCTAGCTACTCAAGAGGCTGAGCTGGGAGG AAAATTAAATGGGCATGGTGGTGTGTGCCTGTGGTTCTAGCTACTCAAGAGGCTGAGCTGGGAGG T C NCOA2 Ensembl:ENSG00000140396 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1023211638 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103301,RMVar_hsa_circ_252645,RMVar_hsa_circ_68083,RMVar_hsa_circ_106213,RMVar_hsa_circ_74648,RMVar_hsa_circ_252651,RMVar_hsa_circ_74481,RMVar_hsa_circ_362557,RMVar_hsa_circ_53916,RMVar_hsa_circ_2394,RMVar_hsa_circ_284058,RMVar_hsa_circ_72919,RMVar_hsa_circ_252664,RMVar_hsa_circ_252665,RMVar_hsa_circ_318959,RMVar_hsa_circ_355301 35002 RMVar_ID_35002 Human_SNP_ID_367779414 A-to-I Human chr8 - 70380830 70380830 70380830 ACTCAAGTCATCTGCCTAACTTGGCCTCCGAAAGTGCTGGGATTACAGACGGGAGCCACGGCCAC ACTCAAGTCATCTGCCTAACTTGGCCTCCGAAGGTGCTGGGATTACAGACGGGAGCCACGGCCAC T C NCOA2 Ensembl:ENSG00000140396 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1044621784 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16466140 RMVar_hsa_circ_103301,RMVar_hsa_circ_252645,RMVar_hsa_circ_106213,RMVar_hsa_circ_252651 35003 RMVar_ID_35003 Human_SNP_ID_367779449 A-to-I Human chr8 - 70380968 70380968 70380968 CCTGGACTCAGGTGATCCTCCTACCTCATCCCAAGTAGTCGGGACCACAGGCGGGCACCACCACA CCTGGACTCAGGTGATCCTCCTACCTCATCCCGAGTAGTCGGGACCACAGGCGGGCACCACCACA T C NCOA2 Ensembl:ENSG00000140396 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs918534021 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103301,RMVar_hsa_circ_252645,RMVar_hsa_circ_106213,RMVar_hsa_circ_252651 35004 RMVar_ID_35004 Human_SNP_ID_367781806 A-to-I Human chr8 - 70390684 70390684 70390684 TAGCTCACTGCAGCCTCAAACTCCTGGGCTCAAGTGATCCTCTCACCTCTGCCTCCTGAGTAGCT TAGCTCACTGCAGCCTCAAACTCCTGGGCTCAGGTGATCCTCTCACCTCTGCCTCCTGAGTAGCT T C NCOA2 Ensembl:ENSG00000140396 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs995978359 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103301,RMVar_hsa_circ_252645,RMVar_hsa_circ_106213,RMVar_hsa_circ_252651 35005 RMVar_ID_35005 Human_SNP_ID_367826687 A-to-I Human chr8 - 70577086 70577086 70577086 TGGGAACTTTGGACCTGCTGAATGGCGGGACTAAAAGGGCTATAGCACAAACAAGGCTGAAATAT TGGGAACTTTGGACCTGCTGAATGGCGGGACTGAAAGGGCTATAGCACAAACAAGGCTGAAATAT T C TRAM1 Ensembl:ENSG00000067167 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909008715 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94515,RMVar_hsa_circ_252672 35006 RMVar_ID_35006 Human_SNP_ID_367826843 A-to-I Human chr8 - 70577701 70577701 70577701 GCACAGCTCTTCTCTCTTTCTTGTCATCCACAACGTGGTGAGCAGAGGGGCATGTTTCAGCCTTG GCACAGCTCTTCTCTCTTTCTTGTCATCCACAGCGTGGTGAGCAGAGGGGCATGTTTCAGCCTTG T C TRAM1 Ensembl:ENSG00000067167 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1167501345 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94515,RMVar_hsa_circ_252672 35007 RMVar_ID_35007 Human_SNP_ID_367841504 A-to-I Human chr8 + 70640162 70640162 70640162 TAAAAAATTTCTTGTAGAGATGAGGTCTCACTATGTTGCCCAAGCTTGTCTCGGACTCCTGGGCT TAAAAAATTTCTTGTAGAGATGAGGTCTCACTCTGTTGCCCAAGCTTGTCTCGGACTCCTGGGCT A C LACTB2-AS1 Ensembl:ENSG00000246366 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs983516984 Functional Loss SNV dbSNP153 33..33 33 - - - 35008 RMVar_ID_35008 Human_SNP_ID_368480104 A-to-I Human chr8 - 73277609 73277609 73277609 TGAAAAGAAAAAGTTCTATGGTCCACAAAGGCAGAAGATGATGTTTATGGGATTTATCTGTCTGG TGAAAAGAAAAAGTTCTATGGTCCACAAAGGCGGAAGATGATGTTTATGGGATTTATCTGTCTGG T C PRXL2AP2 Ensembl:ENSG00000254213 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878893777 Functional Loss SNV dbSNP153 33..33 33 - - - 35009 RMVar_ID_35009 Human_SNP_ID_368480123 A-to-I Human chr8 - 73277658 73277658 73277658 ATGAAGTGAAGGATTTCCAGCCTTATTTTAAAAGAGAAACCTTCCTGGATGAAAAGAAAAAGTTC ATGAAGTGAAGGATTTCCAGCCTTATTTTAAAGGAGAAACCTTCCTGGATGAAAAGAAAAAGTTC T C PRXL2AP2 Ensembl:ENSG00000254213 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878876229 Functional Loss SNV dbSNP153 33..33 33 - - - 35010 RMVar_ID_35010 Human_SNP_ID_368489420 A-to-I Human chr8 + 73312398 73312398 73312398 ACTAGCGGAACATTTGAGCAACATCAGCAGTTAGTACTTAACACACACGCACAAGAATACTCCTA ACTAGCGGAACATTTGAGCAACATCAGCAGTTGGTACTTAACACACACGCACAAGAATACTCCTA A G RDH10 Ensembl:ENSG00000121039 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903806244 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3168451 RMVar_hsa_circ_63513 35011 RMVar_ID_35011 Human_SNP_ID_368492176 A-to-I Human chr8 + 73323826 73323826 73323826 GGCATGCGCCACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGG GGCATGCGCCACCACGCCCAGCTAATTTTTGTGTTTTTAGTAGAGACGGGGTTTCACCATGTTGG A G RDH10 Ensembl:ENSG00000121039 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1264135429 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90998,RMVar_hsa_circ_252736 35012 RMVar_ID_35012 Human_SNP_ID_368528076 A-to-I Human chr8 - 73471289 73471289 73471289 GTGTGCCTGTAGTCCTGGCTACCTGGGAGGCCAAGGCTGGAGGATTGCTTGAGCCTGGGAGGTCA GTGTGCCTGTAGTCCTGGCTACCTGGGAGGCCGAGGCTGGAGGATTGCTTGAGCCTGGGAGGTCA T C STAU2 Ensembl:ENSG00000040341 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1255032800 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74617 35013 RMVar_ID_35013 Human_SNP_ID_368541697 A-to-I Human chr8 - 73532622 73532620 73532622 CTCATTTTTAAAATTTTTTATATTTTTGAGACAGGGTCTCGCTCTGTCACTGAGGCTGGAGTACA CTCATTTTTAAAATTTTTTATATTTTTGAGAC__GGTCTCGCTCTGTCACTGAGGCTGGAGTACA CCT C STAU2 Ensembl:ENSG00000040341 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs766194871 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_252737,RMVar_hsa_circ_344776,RMVar_hsa_circ_74617,RMVar_hsa_circ_353203,RMVar_hsa_circ_367583,RMVar_hsa_circ_351591,RMVar_hsa_circ_305357,RMVar_hsa_circ_330154,RMVar_hsa_circ_12523 35014 RMVar_ID_35014 Human_SNP_ID_368584936 A-to-I Human chr8 - 73715399 73715399 73715399 CAGGCTAGAGTGTAGTGGTGCCATCTCGGTTCACTGCAACTTCCACCTCCCAGGTTCAAGCGATT CAGGCTAGAGTGTAGTGGTGCCATCTCGGTTCGCTGCAACTTCCACCTCCCAGGTTCAAGCGATT T C STAU2,AC022826.2 Ensembl:ENSG00000040341,Ensembl:ENSG00000258677 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1409115611 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5048,RMVar_hsa_circ_344776,RMVar_hsa_circ_330154,RMVar_hsa_circ_252738,RMVar_hsa_circ_114517,RMVar_hsa_circ_285401,RMVar_hsa_circ_43107,RMVar_hsa_circ_298916,RMVar_hsa_circ_311354,RMVar_hsa_circ_62738,RMVar_hsa_circ_283002,RMVar_hsa_circ_33197,RMVar_hsa_circ_332414,RMVar_hsa_circ_14199,RMVar_hsa_circ_305225,RMVar_hsa_circ_252749,RMVar_hsa_circ_252748,RMVar_hsa_circ_285460,RMVar_hsa_circ_282825,RMVar_hsa_circ_252751,RMVar_hsa_circ_252752,RMVar_hsa_circ_57687 35015 RMVar_ID_35015 Human_SNP_ID_368591491 A-to-I Human chr8 - 73741615 73741615 73741615 CCAGCTACTGGGGAGTCTGAGGCAGGAGAATCACTTGAGCCTGGTAGGTGGAGGTTGCAGTGAGC CCAGCTACTGGGGAGTCTGAGGCAGGAGAATCCCTTGAGCCTGGTAGGTGGAGGTTGCAGTGAGC T G STAU2,AC022826.2 Ensembl:ENSG00000040341,Ensembl:ENSG00000258677 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1426416913 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16470425 RMVar_hsa_circ_252738,RMVar_hsa_circ_114517,RMVar_hsa_circ_344698 35016 RMVar_ID_35016 Human_SNP_ID_368591656 A-to-I Human chr8 - 73742298 73742298 73742298 GAACTCCTGACCTCAGGTGATCCGTCCGCCTCAGACTCCAAAAGTGCTGGGATTACAGGCGTGAG GAACTCCTGACCTCAGGTGATCCGTCCGCCTCGGACTCCAAAAGTGCTGGGATTACAGGCGTGAG T C STAU2,AC022826.2 Ensembl:ENSG00000040341,Ensembl:ENSG00000258677 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs578016508 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_986512,Human_Splice_Rec_986513,Human_Splice_Rec_986540,Human_Splice_Rec_986541 RMVar_hsa_circ_252738,RMVar_hsa_circ_114517,RMVar_hsa_circ_344698 35017 RMVar_ID_35017 Human_SNP_ID_368591662 A-to-I Human chr8 - 73742316 73742314 73742316 GTTCGCCAGGCTAGTCTCGAACTCCTGACCTCAGGTGATCCGTCCGCCTCAGACTCCAAAAGTGC GTTCGCCAGGCTAGTCTCGAACTCCTGACCTC__GTGATCCGTCCGCCTCAGACTCCAAAAGTGC CCT C STAU2,AC022826.2 Ensembl:ENSG00000040341,Ensembl:ENSG00000258677 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1245789631 Functional Loss DEL dbSNP153 33..34 33 - - - Human_Splice_Rec_986512,Human_Splice_Rec_986513,Human_Splice_Rec_986540,Human_Splice_Rec_986541 RMVar_hsa_circ_252738,RMVar_hsa_circ_114517,RMVar_hsa_circ_344698 35018 RMVar_ID_35018 Human_SNP_ID_368591685 A-to-I Human chr8 - 73742365 73742365 73742365 CTCCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGACGATTTTGCCGTGTTCGCCAGGCTAGTC CTCCATGCCTGGCTAATTTTTGTATTTTTAGTGGAGACGATTTTGCCGTGTTCGCCAGGCTAGTC T C STAU2,AC022826.2 Ensembl:ENSG00000040341,Ensembl:ENSG00000258677 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs780384995 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_252738,RMVar_hsa_circ_114517,RMVar_hsa_circ_344698 35019 RMVar_ID_35019 Human_SNP_ID_368609642 A-to-I Human chr8 - 73813820 73813820 73813820 TGAACCTGGGAGGCGGGGATTGCAGTGAGCCAAGGTCGTACCATTGCACTCCAGCCTGGGCAACA TGAACCTGGGAGGCGGGGATTGCAGTGAGCCAGGGTCGTACCATTGCACTCCAGCCTGGGCAACA T C UBE2W,AC022826.2 Ensembl:ENSG00000104343,Ensembl:ENSG00000258677 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1452609366 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56332,RMVar_hsa_circ_271367,RMVar_hsa_circ_331467,RMVar_hsa_circ_252756 35020 RMVar_ID_35020 Human_SNP_ID_368609650 A-to-I Human chr8 - 73813849 73813844 73813850 CAGGTGGAGGCTGAGGCAGGAGAATCACTTGAACCTGGGAGGCGGGGATTGCAGTGAGCCAAGGT CAGGTGGAGGCTGAGGCAGGAGAATCACTTG______GGAGGCGGGGATTGCAGTGAGCCAAGGT CCAGGTT C UBE2W,AC022826.2 Ensembl:ENSG00000104343,Ensembl:ENSG00000258677 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1391360004 Functional Loss DEL dbSNP153 32..37 33 - - - Human_RBP_ID_26182075 RMVar_hsa_circ_56332,RMVar_hsa_circ_271367,RMVar_hsa_circ_331467,RMVar_hsa_circ_252756 35021 RMVar_ID_35021 Human_SNP_ID_368614721 A-to-I Human chr8 - 73834717 73834717 73834717 TGTAGTAGAGACGAGGTTTCGCCATGTTGCCCAGGCTAGTCTTGAACTCCTGACCTCAGGCATTA TGTAGTAGAGACGAGGTTTCGCCATGTTGCCCGGGCTAGTCTTGAACTCCTGACCTCAGGCATTA T C UBE2W,AC022826.2 Ensembl:ENSG00000104343,Ensembl:ENSG00000258677 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348875307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16471464 35022 RMVar_ID_35022 Human_SNP_ID_368616047 A-to-I Human chr8 - 73839902 73839902 73839902 GTGAAACCCCATCTCACCATGTTTAAAATACAAAATTTAGCCAGGTGTGGTGATGCATGCCTGGA GTGAAACCCCATCTCACCATGTTTAAAATACACAATTTAGCCAGGTGTGGTGATGCATGCCTGGA T G UBE2W,AC022826.2 Ensembl:ENSG00000104343,Ensembl:ENSG00000258677 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1301193026 Functional Loss SNV dbSNP153 33..33 33 - - - 35023 RMVar_ID_35023 Human_SNP_ID_368620715 A-to-I Human chr8 - 73856597 73856597 73856597 TAATCTCAGCATTTTGGGAGGCCAGGGCGGGCAGATCACTTGAGGTCAGGAGTTCGAGCCAGACC TAATCTCAGCATTTTGGGAGGCCAGGGCGGGCTGATCACTTGAGGTCAGGAGTTCGAGCCAGACC T A UBE2W,AC022826.2 Ensembl:ENSG00000104343,Ensembl:ENSG00000258677 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1213766403 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_796577,Human_RBP_ID_26182208 35024 RMVar_ID_35024 Human_SNP_ID_368620716 A-to-I Human chr8 - 73856597 73856597 73856597 TAATCTCAGCATTTTGGGAGGCCAGGGCGGGCAGATCACTTGAGGTCAGGAGTTCGAGCCAGACC TAATCTCAGCATTTTGGGAGGCCAGGGCGGGCGGATCACTTGAGGTCAGGAGTTCGAGCCAGACC T C UBE2W,AC022826.2 Ensembl:ENSG00000104343,Ensembl:ENSG00000258677 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1213766403 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_796577,Human_RBP_ID_26182208 35025 RMVar_ID_35025 Human_SNP_ID_368625421 A-to-I Human chr8 - 73873038 73873038 73873038 AGCCAGGCGTGGTAGAGCGCATCTGTAATCCCAGTTATTTGAGAGGCTGAGGCAGGAGAATCCCT AGCCAGGCGTGGTAGAGCGCATCTGTAATCCCGGTTATTTGAGAGGCTGAGGCAGGAGAATCCCT T C UBE2W,AC022826.2 Ensembl:ENSG00000104343,Ensembl:ENSG00000258677 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1167839202 Functional Loss SNV dbSNP153 33..33 33 - - - 35026 RMVar_ID_35026 Human_SNP_ID_368625423 A-to-I Human chr8 - 73873043 73873043 73873043 AAATTAGCCAGGCGTGGTAGAGCGCATCTGTAATCCCAGTTATTTGAGAGGCTGAGGCAGGAGAA AAATTAGCCAGGCGTGGTAGAGCGCATCTGTAGTCCCAGTTATTTGAGAGGCTGAGGCAGGAGAA T C UBE2W,AC022826.2 Ensembl:ENSG00000104343,Ensembl:ENSG00000258677 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs952795384 Functional Loss SNV dbSNP153 33..33 33 - - - 35027 RMVar_ID_35027 Human_SNP_ID_368625427 A-to-I Human chr8 - 73873057 73873057 73873057 TAAAAATACAAAAAAAATTAGCCAGGCGTGGTAGAGCGCATCTGTAATCCCAGTTATTTGAGAGG TAAAAATACAAAAAAAATTAGCCAGGCGTGGTTGAGCGCATCTGTAATCCCAGTTATTTGAGAGG T A UBE2W,AC022826.2 Ensembl:ENSG00000104343,Ensembl:ENSG00000258677 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1177877224 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16472385 35028 RMVar_ID_35028 Human_SNP_ID_368644455 A-to-I Human chr8 - 73948013 73948013 73948013 TAATTTTGTATTTTTAGTACAGATGGGGTTTCACTATGTTAGTCAGGCTGCTCTCGAACTCTTGA TAATTTTGTATTTTTAGTACAGATGGGGTTTCGCTATGTTAGTCAGGCTGCTCTCGAACTCTTGA T C ELOC Ensembl:ENSG00000154582 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569813986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16472725 35029 RMVar_ID_35029 Human_SNP_ID_368644860 A-to-I Human chr8 - 73949628 73949628 73949628 GTCACATTTGTATGATTCCATTTTTATGAAATATCCAGAGTAGGTAAATCCATAGAGACGGAAAG GTCACATTTGTATGATTCCATTTTTATGAAATGTCCAGAGTAGGTAAATCCATAGAGACGGAAAG T C ELOC Ensembl:ENSG00000154582 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270847967 Functional Loss SNV dbSNP153 33..33 33 - - - 35030 RMVar_ID_35030 Human_SNP_ID_368644861 A-to-I Human chr8 - 73949630 73949630 73949630 ATGTCACATTTGTATGATTCCATTTTTATGAAATATCCAGAGTAGGTAAATCCATAGAGACGGAA ATGTCACATTTGTATGATTCCATTTTTATGAAGTATCCAGAGTAGGTAAATCCATAGAGACGGAA T C ELOC Ensembl:ENSG00000154582 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1160111350 Functional Loss SNV dbSNP153 33..33 33 - - - 35031 RMVar_ID_35031 Human_SNP_ID_368650364 A-to-I Human chr8 - 73970234 73970230 73970234 TATGCTCATATTTATTTTTGAGTCAGAGTCTCACTCTGTTCTGCACTCCCAGGCTGGAGTGCAGT TATGCTCATATTTATTTTTGAGTCAGAGTCTC____TGTTCTGCACTCCCAGGCTGGAGTGCAGT AGAGT A ELOC Ensembl:ENSG00000154582 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1468644307 Functional Loss DEL dbSNP153 33..36 33 - - - 35032 RMVar_ID_35032 Human_SNP_ID_368803241 A-to-I Human chr8 - 74604194 74604194 74604194 GAAGGTGGATTAAATATCACTCTCACCATCCGACTACTTATGCATGGAAAGGAAGTTGGCAGTAT GAAGGTGGATTAAATATCACTCTCACCATCCGGCTACTTATGCATGGAAAGGAAGTTGGCAGTAT T C AC115837.1 Ensembl:ENSG00000253341 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879008325 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3170018,Human_RBP_ID_7870845 Human_miRNA_ID_1895024 35033 RMVar_ID_35033 Human_SNP_ID_368803248 A-to-I Human chr8 - 74604211 74604211 74604211 TGGAAACCAGTGTGATTGAAGGTGGATTAAATATCACTCTCACCATCCGACTACTTATGCATGGA TGGAAACCAGTGTGATTGAAGGTGGATTAAATGTCACTCTCACCATCCGACTACTTATGCATGGA T C AC115837.1 Ensembl:ENSG00000253341 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879178757 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5629268 Human_miRNA_ID_1819044,Human_miRNA_ID_1853479 35034 RMVar_ID_35034 Human_SNP_ID_368803253 A-to-I Human chr8 - 74604235 74604235 74604235 AGCTCCCCAGAACACTGCTCGACATGGAAACCAGTGTGATTGAAGGTGGATTAAATATCACTCTC AGCTCCCCAGAACACTGCTCGACATGGAAACCGGTGTGATTGAAGGTGGATTAAATATCACTCTC T C AC115837.1 Ensembl:ENSG00000253341 Pseudogene exon GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs879065967 Functional Loss SNV dbSNP153 33..33 33 - - - 35035 RMVar_ID_35035 Human_SNP_ID_275443338 A-to-I Human chr6 - 45362044 45362044 45362044 TGTTGTTGTTGTTGTTGTTGTTTTTGAGAGGAATCTAGCTTTGTTGCCCAGGCGCTGGAGTGCAG TGTTGTTGTTGTTGTTGTTGTTTTTGAGAGGATTCTAGCTTTGTTGCCCAGGCGCTGGAGTGCAG T A SUPT3H Ensembl:ENSG00000196284 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1028804337 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3810732,Human_RBP_ID_15839358,Human_RBP_ID_17161488,Human_RBP_ID_21349156 RMVar_hsa_circ_319157,RMVar_hsa_circ_333604,RMVar_hsa_circ_281622,RMVar_hsa_circ_238818,RMVar_hsa_circ_321036,RMVar_hsa_circ_282281,RMVar_hsa_circ_323640,RMVar_hsa_circ_32056,RMVar_hsa_circ_293828,RMVar_hsa_circ_238824,RMVar_hsa_circ_58289,RMVar_hsa_circ_288304,RMVar_hsa_circ_238826,RMVar_hsa_circ_287884,RMVar_hsa_circ_238828 35036 RMVar_ID_35036 Human_SNP_ID_275443339 A-to-I Human chr6 - 45362044 45362044 45362044 TGTTGTTGTTGTTGTTGTTGTTTTTGAGAGGAATCTAGCTTTGTTGCCCAGGCGCTGGAGTGCAG TGTTGTTGTTGTTGTTGTTGTTTTTGAGAGGAGTCTAGCTTTGTTGCCCAGGCGCTGGAGTGCAG T C SUPT3H Ensembl:ENSG00000196284 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1028804337 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3810732,Human_RBP_ID_15839358,Human_RBP_ID_17161488,Human_RBP_ID_21349156 RMVar_hsa_circ_319157,RMVar_hsa_circ_333604,RMVar_hsa_circ_281622,RMVar_hsa_circ_238818,RMVar_hsa_circ_321036,RMVar_hsa_circ_282281,RMVar_hsa_circ_323640,RMVar_hsa_circ_32056,RMVar_hsa_circ_293828,RMVar_hsa_circ_238824,RMVar_hsa_circ_58289,RMVar_hsa_circ_288304,RMVar_hsa_circ_238826,RMVar_hsa_circ_287884,RMVar_hsa_circ_238828 35037 RMVar_ID_35037 Human_SNP_ID_275760394 A-to-I Human chr6 + 46656210 46656208 46656210 TATTATTTAGGTTTTTTTTTTGAGATGGAGTCACACTCTGTCGCCCAGGCTGTAGTGCAGTGGCG TATTATTTAGGTTTTTTTTTTGAGATGGAGT__CACTCTGTCGCCCAGGCTGTAGTGCAGTGGCG TCA T SLC25A27 Ensembl:ENSG00000153291 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1164851235 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_22137,RMVar_hsa_circ_342195,RMVar_hsa_circ_238852 35038 RMVar_ID_35038 Human_SNP_ID_275760396 A-to-I Human chr6 + 46656212 46656212 46656212 TTATTTAGGTTTTTTTTTTGAGATGGAGTCACACTCTGTCGCCCAGGCTGTAGTGCAGTGGCGCC TTATTTAGGTTTTTTTTTTGAGATGGAGTCACGCTCTGTCGCCCAGGCTGTAGTGCAGTGGCGCC A G SLC25A27 Ensembl:ENSG00000153291 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904344462 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22137,RMVar_hsa_circ_342195,RMVar_hsa_circ_238852 35039 RMVar_ID_35039 Human_SNP_ID_275760463 A-to-I Human chr6 + 46656401 46656401 46656401 AGAGTCTCGCTCTGTTGCCCAGGCTGGAGCACAGTGGTGTGACCCTGGCTCACTGCAACCTTTGT AGAGTCTCGCTCTGTTGCCCAGGCTGGAGCACGGTGGTGTGACCCTGGCTCACTGCAACCTTTGT A G SLC25A27 Ensembl:ENSG00000153291 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913225691 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22137,RMVar_hsa_circ_342195,RMVar_hsa_circ_238852 35040 RMVar_ID_35040 Human_SNP_ID_275760464 A-to-I Human chr6 + 46656425 46656425 46656425 TGGAGCACAGTGGTGTGACCCTGGCTCACTGCAACCTTTGTCTCCCGAGTTCAAGCGATTCTCCT TGGAGCACAGTGGTGTGACCCTGGCTCACTGCCACCTTTGTCTCCCGAGTTCAAGCGATTCTCCT A C SLC25A27 Ensembl:ENSG00000153291 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,cerebellum - 29129909,30559470 RNA-Seq:(High) rs939337510 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22137,RMVar_hsa_circ_342195,RMVar_hsa_circ_238852 35041 RMVar_ID_35041 Human_SNP_ID_275760502 A-to-I Human chr6 + 46656621 46656621 46656621 TTGTATTTTTAGTAGAGACGGGGTTTCACCATATTGATCAGGTTGGTCCCAAACTCCTGACCTCA TTGTATTTTTAGTAGAGACGGGGTTTCACCATTTTGATCAGGTTGGTCCCAAACTCCTGACCTCA A T SLC25A27 Ensembl:ENSG00000153291 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs1014107362 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22137,RMVar_hsa_circ_342195,RMVar_hsa_circ_238852 35042 RMVar_ID_35042 Human_SNP_ID_275760503 A-to-I Human chr6 + 46656628 46656628 46656628 TTTAGTAGAGACGGGGTTTCACCATATTGATCAGGTTGGTCCCAAACTCCTGACCTCAGGTGATC TTTAGTAGAGACGGGGTTTCACCATATTGATCTGGTTGGTCCCAAACTCCTGACCTCAGGTGATC A T SLC25A27 Ensembl:ENSG00000153291 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs534932845 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22137,RMVar_hsa_circ_342195,RMVar_hsa_circ_238852 35043 RMVar_ID_35043 Human_SNP_ID_275760512 A-to-I Human chr6 + 46656653 46656653 46656653 ATTGATCAGGTTGGTCCCAAACTCCTGACCTCAGGTGATCCACCTGACTTGGCCTCCCAAAGTGC ATTGATCAGGTTGGTCCCAAACTCCTGACCTCGGGTGATCCACCTGACTTGGCCTCCCAAAGTGC A G SLC25A27 Ensembl:ENSG00000153291 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs919241873 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26011240 RMVar_hsa_circ_22137,RMVar_hsa_circ_342195,RMVar_hsa_circ_238852 35044 RMVar_ID_35044 Human_SNP_ID_275760516 A-to-I Human chr6 + 46656679 46656679 46656679 GACCTCAGGTGATCCACCTGACTTGGCCTCCCAAAGTGCTAGGATTACAGGCGTGAGCCGCCGTG GACCTCAGGTGATCCACCTGACTTGGCCTCCCGAAGTGCTAGGATTACAGGCGTGAGCCGCCGTG A G SLC25A27 Ensembl:ENSG00000153291 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1261441306 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22137,RMVar_hsa_circ_342195,RMVar_hsa_circ_238852 35045 RMVar_ID_35045 Human_SNP_ID_275760580 A-to-I Human chr6 + 46656908 46656908 46656908 ATGAAGCAAGCCAGATACAGTGGCTTATGCCTATAATCCCAGCAGTTTGGAAAGCCGAGGCGGGA ATGAAGCAAGCCAGATACAGTGGCTTATGCCTGTAATCCCAGCAGTTTGGAAAGCCGAGGCGGGA A G SLC25A27 Ensembl:ENSG00000153291 Protein coding intron GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;ASD brains,frontal_cortex;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,30559470,31158229,31158229 RNA-Seq:(High) rs1400646760 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26011244 RMVar_hsa_circ_22137,RMVar_hsa_circ_342195,RMVar_hsa_circ_238852 35046 RMVar_ID_35046 Human_SNP_ID_275760610 A-to-I Human chr6 + 46657037 46657037 46657037 AGAGTAAGAAAATTAGCCAGGCCTGGTGGCACATGACTGTAGTCCCCACTACTTGGGAGGCTGAG AGAGTAAGAAAATTAGCCAGGCCTGGTGGCACGTGACTGTAGTCCCCACTACTTGGGAGGCTGAG A G SLC25A27 Ensembl:ENSG00000153291 Protein coding intron GSE47997;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 23474544,29129909,31158229,31158229 RNA-Seq:(High) rs899605483 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15839633 RMVar_hsa_circ_22137,RMVar_hsa_circ_342195,RMVar_hsa_circ_238852 35047 RMVar_ID_35047 Human_SNP_ID_275772784 A-to-I Human chr6 + 46701935 46701935 46701935 TGTGGCCAATCAGTCAGAAGCTGCCCTTGAACAAGTGGCATCTTACGCAGACCAACAGAGTATTT TGTGGCCAATCAGTCAGAAGCTGCCCTTGAACGAGTGGCATCTTACGCAGACCAACAGAGTATTT A G TDRD6 Ensembl:ENSG00000180113 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs764788432 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_775716,Human_Splice_Rec_775722,Human_Splice_Rec_775730 35048 RMVar_ID_35048 Human_SNP_ID_276506037 A-to-I Human chr6 + 49473893 49473893 49473893 TTGCAATCCTAGTCTCTGATAAAACAGACTTTAAACCAACAAAGATCAAAAGAGACAAAGAAGAC TTGCAATCCTAGTCTCTGATAAAACAGACTTTCAACCAACAAAGATCAAAAGAGACAAAGAAGAC A C CENPQ Ensembl:ENSG00000031691 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1180449614 Functional Loss SNV dbSNP153 33..33 33 - - - 35049 RMVar_ID_35049 Human_SNP_ID_276526549 A-to-I Human chr6 - 49555647 49555647 49555647 AAAATTAGCCGGGCGTGATGGCGAGCGCCTGTAGTCCCGGCTGCTCGGGAGGCTGAGGCAGGAGA AAAATTAGCCGGGCGTGATGGCGAGCGCCTGTGGTCCCGGCTGCTCGGGAGGCTGAGGCAGGAGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1290519233 Functional Loss SNV dbSNP153 33..33 33 - - - 35050 RMVar_ID_35050 Human_SNP_ID_277267137 A-to-I Human chr6 + 52481787 52481787 52481787 GCCTCCTTGGCCTCCCAAAGTGCTAGGATTACAGGCGTGAGCCATTGCTCCTGGCCTGGGTGAAA GCCTCCTTGGCCTCCCAAAGTGCTAGGATTACGGGCGTGAGCCATTGCTCCTGGCCTGGGTGAAA A G EFHC1 Ensembl:ENSG00000096093 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1341536378 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_238952,RMVar_hsa_circ_238950,RMVar_hsa_circ_305388,RMVar_hsa_circ_378141,RMVar_hsa_circ_284140,RMVar_hsa_circ_363225 35051 RMVar_ID_35051 Human_SNP_ID_277269511 A-to-I Human chr6 + 52492632 52492632 52492632 CTTTCTTTCTTTTTAAAAAAATAAATTTTTTTAGAGATGGGATCTCACTCTGTCATACAGGCTGG CTTTCTTTCTTTTTAAAAAAATAAATTTTTTTGGAGATGGGATCTCACTCTGTCATACAGGCTGG A G EFHC1 Ensembl:ENSG00000096093 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs3177234 Functional Loss SNV dbSNP153 33..33 33 - - - 35052 RMVar_ID_35052 Human_SNP_ID_277269525 A-to-I Human chr6 + 52492684 52492684 52492684 TCATACAGGCTGGAGTGTGGTGGCACTATCCTAGTTCTATGAAGCCTCAGACTCCTGGGCTCAAG TCATACAGGCTGGAGTGTGGTGGCACTATCCTGGTTCTATGAAGCCTCAGACTCCTGGGCTCAAG A G EFHC1 Ensembl:ENSG00000096093 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs956711937 Functional Loss SNV dbSNP153 33..33 33 - - - 35053 RMVar_ID_35053 Human_SNP_ID_277269885 A-to-I Human chr6 + 52493537 52493524 52493537 AGCCAGGTGTGGTGGCGTGTGCCTGTAGTCCCAGCCACTCGGGAGGCTTAAATGGGAGAATCACT AGCCAGGTGTGGTGGCGTGT_____________GCCACTCGGGAGGCTTAAATGGGAGAATCACT TGCCTGTAGTCCCA T EFHC1 Ensembl:ENSG00000096093 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1027664351 Functional Loss DEL dbSNP153 21..33 33 - - - 35054 RMVar_ID_35054 Human_SNP_ID_277270560 A-to-I Human chr6 + 52495607 52495607 52495607 GCTGTTTTGTTTTGTTTTTGTGTTTGTTTTTTAGAGACAGGGTCTTACTCTGTTGCCAGACTGGA GCTGTTTTGTTTTGTTTTTGTGTTTGTTTTTTGGAGACAGGGTCTTACTCTGTTGCCAGACTGGA A G EFHC1 Ensembl:ENSG00000096093 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs767275665 Functional Loss SNV dbSNP153 33..33 33 - - - 35055 RMVar_ID_35055 Human_SNP_ID_277284928 A-to-I Human chr6 - 52555003 52555003 52555003 AAGTCAGGATTGACTAGAAGTTGGCCAGGCACAGTGGCTCACACTTGTTATCTCAGCACTTCGGG AAGTCAGGATTGACTAGAAGTTGGCCAGGCACCGTGGCTCACACTTGTTATCTCAGCACTTCGGG T G TRAM2 Ensembl:ENSG00000065308 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1338003956 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269571,RMVar_hsa_circ_238959,RMVar_hsa_circ_110892 35056 RMVar_ID_35056 Human_SNP_ID_277315974 A-to-I Human chr6 + 52683349 52683349 52683349 GGATGTGGTTGTACATGGCTGTAATCTCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCTTGAA GGATGTGGTTGTACATGGCTGTAATCTCAGCTGCTCGGGAGGCTGAGGCAGGAGAATTGCTTGAA A G TMEM14A Ensembl:ENSG00000096092 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1409890569 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127811,RMVar_hsa_circ_84731,RMVar_hsa_circ_238963,RMVar_hsa_circ_238964 35057 RMVar_ID_35057 Human_SNP_ID_277316140 A-to-I Human chr6 + 52683843 52683843 52683843 CTCCATGTTGGTCAGACTGGCCTCAAACTCCCAACATCAGGTGATCCACCCATCTCTGCCTCCCA CTCCATGTTGGTCAGACTGGCCTCAAACTCCCTACATCAGGTGATCCACCCATCTCTGCCTCCCA A T TMEM14A Ensembl:ENSG00000096092 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs966307600 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127811,RMVar_hsa_circ_84731,RMVar_hsa_circ_238963,RMVar_hsa_circ_238964 35058 RMVar_ID_35058 Human_SNP_ID_277399470 A-to-I Human chr6 - 52993017 52993017 52993017 CTCACTGCAACCTCCGCCTCCCAGGATCAAGCAATTCCCCTGCCTCAGCCTACCTAGTAGCTGGG CTCACTGCAACCTCCGCCTCCCAGGATCAAGCGATTCCCCTGCCTCAGCCTACCTAGTAGCTGGG T C GSTA4 Ensembl:ENSG00000170899 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1029225691 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26013392 35059 RMVar_ID_35059 Human_SNP_ID_277399485 A-to-I Human chr6 - 52993077 52993076 52993077 TTTTTTTTTGACGGAGGCTGGCTCTGTAGCCCAGGCTGGAGTGCAGTGGTGTGATCTCGGCTCAC TTTTTTTTTGACGGAGGCTGGCTCTGTAGCCC_GGCTGGAGTGCAGTGGTGTGATCTCGGCTCAC CT C GSTA4 Ensembl:ENSG00000170899 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1204871724 Functional Loss DEL dbSNP153 33..33 33 - - - 35060 RMVar_ID_35060 Human_SNP_ID_277418613 A-to-I Human chr6 + 53076044 53076044 53076044 GGGATTACAGGCGTGAGCCACCGCGCCCAGCCAGATGCTAATATTTTTGATGTTGTGTTTTGGAA GGGATTACAGGCGTGAGCCACCGCGCCCAGCCCGATGCTAATATTTTTGATGTTGTGTTTTGGAA A C FBXO9 Ensembl:ENSG00000112146 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1267383066 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118117,RMVar_hsa_circ_238974,RMVar_hsa_circ_300138,RMVar_hsa_circ_310962,RMVar_hsa_circ_273816,RMVar_hsa_circ_238975,RMVar_hsa_circ_238973,RMVar_hsa_circ_375250,RMVar_hsa_circ_238976,RMVar_hsa_circ_238977 35061 RMVar_ID_35061 Human_SNP_ID_277420153 A-to-I Human chr6 + 53082601 53082601 53082601 TCATTGGAGCAGTTGTCGCTGGTGTGCAGAGGATTCTACATCTGTGCCAGGTACTAAGTTTTTGT TCATTGGAGCAGTTGTCGCTGGTGTGCAGAGGTTTCTACATCTGTGCCAGGTACTAAGTTTTTGT A T FBXO9 Ensembl:ENSG00000112146 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1282715197 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_666300,Human_RBP_ID_948829,Human_RBP_ID_3969186,Human_RBP_ID_8237378,Human_RBP_ID_9400749,Human_RBP_ID_15849409,Human_RBP_ID_18450568,Human_RBP_ID_18867633,Human_RBP_ID_19017180,Human_RBP_ID_27827782 Human_Splice_Rec_778376,Human_Splice_Rec_778377,Human_Splice_Rec_778398,Human_Splice_Rec_778399,Human_Splice_Rec_778422,Human_Splice_Rec_778423,Human_Splice_Rec_778440,Human_Splice_Rec_778441,Human_Splice_Rec_778448,Human_Splice_Rec_778449 RMVar_hsa_circ_300138,RMVar_hsa_circ_238973,RMVar_hsa_circ_375250,RMVar_hsa_circ_50044,RMVar_hsa_circ_238977,RMVar_hsa_circ_356639,RMVar_hsa_circ_101077,RMVar_hsa_circ_61031,RMVar_hsa_circ_238979,RMVar_hsa_circ_238982,RMVar_hsa_circ_374361,RMVar_hsa_circ_275338,RMVar_hsa_circ_238981,RMVar_hsa_circ_367589 35062 RMVar_ID_35062 Human_SNP_ID_277421411 A-to-I Human chr6 + 53088728 53088728 53088728 TCAGGCGATTCTCCTGCCTCAGTCTCCCGAGTAGCCGAGATTACAGGCATGCACCACCACCGCCT TCAGGCGATTCTCCTGCCTCAGTCTCCCGAGTGGCCGAGATTACAGGCATGCACCACCACCGCCT A G FBXO9 Ensembl:ENSG00000112146 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1180225424 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_375250,RMVar_hsa_circ_238977,RMVar_hsa_circ_101077,RMVar_hsa_circ_61031,RMVar_hsa_circ_238979,RMVar_hsa_circ_238982,RMVar_hsa_circ_374361,RMVar_hsa_circ_367589 35063 RMVar_ID_35063 Human_SNP_ID_277424249 A-to-I Human chr6 + 53100709 53100709 53100709 TGCATCTATAAAAATGGGATTATATTGTACAGAATGCTTTGTAAGCTTTCTCTCCCCACATAAGA TGCATCTATAAAAATGGGATTATATTGTACAGGATGCTTTGTAAGCTTTCTCTCCCCACATAAGA A G FBXO9 Ensembl:ENSG00000112146 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1446299604 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1674853,Human_RBP_ID_2023396,Human_RBP_ID_18867671 RMVar_hsa_circ_101077,RMVar_hsa_circ_238979 35064 RMVar_ID_35064 Human_SNP_ID_277466431 A-to-I Human chr6 - 53271367 53271367 53271367 TTTTGTATTTTTAGTAGAGACAGGGTTTCACCATTTTGGCCAGGATGGTGTTGATCTCTTGACCT TTTTGTATTTTTAGTAGAGACAGGGTTTCACCGTTTTGGCCAGGATGGTGTTGATCTCTTGACCT T C ELOVL5 Ensembl:ENSG00000012660 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1381975030 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106233,RMVar_hsa_circ_121642,RMVar_hsa_circ_125654,RMVar_hsa_circ_116206,RMVar_hsa_circ_104715,RMVar_hsa_circ_59935,RMVar_hsa_circ_238984,RMVar_hsa_circ_238986,RMVar_hsa_circ_238988,RMVar_hsa_circ_238987,RMVar_hsa_circ_238985,RMVar_hsa_circ_238991,RMVar_hsa_circ_238992,RMVar_hsa_circ_349433 35065 RMVar_ID_35065 Human_SNP_ID_277471458 A-to-I Human chr6 - 53292534 53292534 53292534 CACCCGCCTTGGCATCCCAAAGTGCTGGGATTACAGGCATGAGCCACCACACCCAGCCCTTGTTT CACCCGCCTTGGCATCCCAAAGTGCTGGGATTGCAGGCATGAGCCACCACACCCAGCCCTTGTTT T C ELOVL5 Ensembl:ENSG00000012660 Protein coding intron GSE100210;GSE99789 HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 29129909,29796672 RNA-Seq:(High) rs981146314 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26013731 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 35066 RMVar_ID_35066 Human_SNP_ID_277471461 A-to-I Human chr6 - 53292574 53292556 53292575 GTTGGCCAGGCTGGTCTTGAACTCCTGACTTCAGGTGATCCACCCGCCTTGGCATCCCAAAGTGC GTTGGCCAGGCTGGTCTTGAACTCCTGACTT___________________GGCATCCCAAAGTGC CAAGGCGGGTGGATCACCTG C ELOVL5 Ensembl:ENSG00000012660 Protein coding intron GSE38233;GSE99789 cultured B-cells;esophageal squamous carcinoma cells,EC109 - 24183664,29796672 RNA-Seq:(High) rs1484550244 Functional Loss DEL dbSNP153 32..50 33 - - - 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 35067 RMVar_ID_35067 Human_SNP_ID_277471481 A-to-I Human chr6 - 53292682 53292682 53292682 ATTTCAAGCGATTCTCCCACCTCAGCCTCCCAAGTAGCTGGGATTACAGGTGTGCAGCACCATGC ATTTCAAGCGATTCTCCCACCTCAGCCTCCCATGTAGCTGGGATTACAGGTGTGCAGCACCATGC T A ELOVL5 Ensembl:ENSG00000012660 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1427445517 Functional Loss SNV dbSNP153 33..33 33 - - - 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 35068 RMVar_ID_35068 Human_SNP_ID_277471486 A-to-I Human chr6 - 53292696 53292696 53292696 GCCTCTTCCTCCCAATTTCAAGCGATTCTCCCACCTCAGCCTCCCAAGTAGCTGGGATTACAGGT GCCTCTTCCTCCCAATTTCAAGCGATTCTCCCCCCTCAGCCTCCCAAGTAGCTGGGATTACAGGT T G ELOVL5 Ensembl:ENSG00000012660 Protein coding intron GSE100210;GSE99789 HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 29129909,29796672 RNA-Seq:(High) rs1456349016 Functional Loss SNV dbSNP153 33..33 33 - - - 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 35069 RMVar_ID_35069 Human_SNP_ID_277471490 A-to-I Human chr6 - 53292708 53292708 53292708 CAGCTCACTGCAGCCTCTTCCTCCCAATTTCAAGCGATTCTCCCACCTCAGCCTCCCAAGTAGCT CAGCTCACTGCAGCCTCTTCCTCCCAATTTCAGGCGATTCTCCCACCTCAGCCTCCCAAGTAGCT T C ELOVL5 Ensembl:ENSG00000012660 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1313756127 Functional Loss SNV dbSNP153 33..33 33 - - - 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 35070 RMVar_ID_35070 Human_SNP_ID_277471495 A-to-I Human chr6 - 53292734 53292734 53292734 CACGCTGGGGTGCAGTGGTACGATCTCAGCTCACTGCAGCCTCTTCCTCCCAATTTCAAGCGATT CACGCTGGGGTGCAGTGGTACGATCTCAGCTCGCTGCAGCCTCTTCCTCCCAATTTCAAGCGATT T C ELOVL5 Ensembl:ENSG00000012660 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1004641968 Functional Loss SNV dbSNP153 33..33 33 - - - 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 35071 RMVar_ID_35071 Human_SNP_ID_277471496 A-to-I Human chr6 - 53292739 53292739 53292739 TTGCCCACGCTGGGGTGCAGTGGTACGATCTCAGCTCACTGCAGCCTCTTCCTCCCAATTTCAAG TTGCCCACGCTGGGGTGCAGTGGTACGATCTCGGCTCACTGCAGCCTCTTCCTCCCAATTTCAAG T C ELOVL5 Ensembl:ENSG00000012660 Protein coding intron GSE100210;GSE99789 HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 29129909,29796672 RNA-Seq:(High) rs933314490 Functional Loss SNV dbSNP153 33..33 33 - - - 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 35072 RMVar_ID_35072 Human_SNP_ID_277471516 A-to-I Human chr6 - 53292777 53292777 53292777 TGTTTTTATTTTCATTTTTGAGACGGAGTCTCACTCTGTTGCCCACGCTGGGGTGCAGTGGTACG TGTTTTTATTTTCATTTTTGAGACGGAGTCTCGCTCTGTTGCCCACGCTGGGGTGCAGTGGTACG T C ELOVL5 Ensembl:ENSG00000012660 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs547041079 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15850731 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 35073 RMVar_ID_35073 Human_SNP_ID_277471690 A-to-I Human chr6 - 53293458 53293458 53293458 CAAAAATTAGCGGGGTGTGGTGGTGTGTGTCTATAGTCCCAGCTACTCTGGAGGCTAAGGCAGGA CAAAAATTAGCGGGGTGTGGTGGTGTGTGTCTGTAGTCCCAGCTACTCTGGAGGCTAAGGCAGGA T C ELOVL5 Ensembl:ENSG00000012660 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs763757195 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_169004 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 35074 RMVar_ID_35074 Human_SNP_ID_277471698 A-to-I Human chr6 - 53293489 53293489 53293489 ATATGGTGAAACCTGGTCTCTACTAAAATTACAAAAATTAGCGGGGTGTGGTGGTGTGTGTCTAT ATATGGTGAAACCTGGTCTCTACTAAAATTACTAAAATTAGCGGGGTGTGGTGGTGTGTGTCTAT T A ELOVL5 Ensembl:ENSG00000012660 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1186137800 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26013745 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 35075 RMVar_ID_35075 Human_SNP_ID_277471722 A-to-I Human chr6 - 53293568 53293568 53293568 CACTCCTGTAATCCCAGTACTTTGGGAGGCCAAGGCAGGTGGGTCCCCTGAGGTCAGGAGTTCCA CACTCCTGTAATCCCAGTACTTTGGGAGGCCATGGCAGGTGGGTCCCCTGAGGTCAGGAGTTCCA T A ELOVL5 Ensembl:ENSG00000012660 Protein coding intron GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs1427555213 Functional Loss SNV dbSNP153 33..33 33 - - - 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 35076 RMVar_ID_35076 Human_SNP_ID_277479670 A-to-I Human chr6 - 53324212 53324212 53324212 GTCTCGTTCTGTCTCCCAGGCTGGAGTGCAGTAGCACAATCTCAGCTCACTGCAACCTCCGCCTT GTCTCGTTCTGTCTCCCAGGCTGGAGTGCAGTGGCACAATCTCAGCTCACTGCAACCTCCGCCTT T C ELOVL5 Ensembl:ENSG00000012660 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355472208 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104715,RMVar_hsa_circ_238984 35077 RMVar_ID_35077 Human_SNP_ID_277481521 A-to-I Human chr6 - 53331582 53331582 53331582 CAGTGATGAACTGCCTATATAATGGTGGTCCCATAAGATTATAATGGAACTGAAAAATTCCTCTT CAGTGATGAACTGCCTATATAATGGTGGTCCCGTAAGATTATAATGGAACTGAAAAATTCCTCTT T C ELOVL5 Ensembl:ENSG00000012660 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1209247283 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104715,RMVar_hsa_circ_238984 35078 RMVar_ID_35078 Human_SNP_ID_277525776 A-to-I Human chr6 - 53504154 53504154 53504154 TTTTAAACCTTTTTTAGAGACAGGGTCTCACTATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCT TTTTAAACCTTTTTTAGAGACAGGGTCTCACTGTGTTGCTCAGGCTGGTCTCGAACTCCTGGGCT T C GCLC Ensembl:ENSG00000001084 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs772370487 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_238999,RMVar_hsa_circ_124846,RMVar_hsa_circ_67784,RMVar_hsa_circ_239000 35079 RMVar_ID_35079 Human_SNP_ID_277525777 A-to-I Human chr6 - 53504154 53504154 53504154 TTTTAAACCTTTTTTAGAGACAGGGTCTCACTATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCT TTTTAAACCTTTTTTAGAGACAGGGTCTCACTCTGTTGCTCAGGCTGGTCTCGAACTCCTGGGCT T G GCLC Ensembl:ENSG00000001084 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs772370487 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_238999,RMVar_hsa_circ_124846,RMVar_hsa_circ_67784,RMVar_hsa_circ_239000 35080 RMVar_ID_35080 Human_SNP_ID_277533033 A-to-I Human chr6 - 53535298 53535298 53535298 GTTGGCCAGGCTGGTCTTGAACTCCTGAGCTCAGGCAGTCCGCCTGCCTTGGCCTCCCAGAGTGC GTTGGCCAGGCTGGTCTTGAACTCCTGAGCTCGGGCAGTCCGCCTGCCTTGGCCTCCCAGAGTGC T C GCLC Ensembl:ENSG00000001084 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167359341 Functional Loss SNV dbSNP153 33..33 33 - - - 35081 RMVar_ID_35081 Human_SNP_ID_277534709 A-to-I Human chr6 - 53541966 53541966 53541966 CTACTCGGGAGGCTGAGATAGAAGGATCGCTTAAGCCTGGGAGTTTGAGGCTGCAGTGAGCCGTG CTACTCGGGAGGCTGAGATAGAAGGATCGCTTGAGCCTGGGAGTTTGAGGCTGCAGTGAGCCGTG T C GCLC Ensembl:ENSG00000001084 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031580385 Functional Loss SNV dbSNP153 33..33 33 - - - 35082 RMVar_ID_35082 Human_SNP_ID_277534723 A-to-I Human chr6 - 53541999 53541999 53541999 TAAAAAATTAGTGGCATGTGCCTGTGGCCCCAACTACTCGGGAGGCTGAGATAGAAGGATCGCTT TAAAAAATTAGTGGCATGTGCCTGTGGCCCCAGCTACTCGGGAGGCTGAGATAGAAGGATCGCTT T C GCLC Ensembl:ENSG00000001084 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs552445540 Functional Loss SNV dbSNP153 33..33 33 - - - 35083 RMVar_ID_35083 Human_SNP_ID_277610158 A-to-I Human chr6 + 53859810 53859810 53859810 TTGCTTTATAATTAAAAAAAAATCCCAGAATGAAATAGACTTGGAAACACAATGGGATAAATGCA TTGCTTTATAATTAAAAAAAAATCCCAGAATGTAATAGACTTGGAAACACAATGGGATAAATGCA A T LRRC1 Ensembl:ENSG00000137269 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs953340364 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_163,RMVar_hsa_circ_330899,RMVar_hsa_circ_364281,RMVar_hsa_circ_239007 35084 RMVar_ID_35084 Human_SNP_ID_278348521 A-to-I Human chr6 - 56788333 56788333 56788333 AAAGTAGCTGGTGGTGCACACCTATAGTCCCAACTACTTGGGAGGCTAAGGCAGGATAATTGCTT AAAGTAGCTGGTGGTGCACACCTATAGTCCCACCTACTTGGGAGGCTAAGGCAGGATAATTGCTT T G DST Ensembl:ENSG00000151914 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251705383 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57037,RMVar_hsa_circ_89652,RMVar_hsa_circ_239126,RMVar_hsa_circ_13312,RMVar_hsa_circ_52272 35085 RMVar_ID_35085 Human_SNP_ID_278384737 A-to-I Human chr6 - 56947428 56947428 56947428 CTGGTCAACATGGTGAAACCCCGTCTTTACTAAAATACAAAAATTAGCTGGGTGTGGTGGCGCAC CTGGTCAACATGGTGAAACCCCGTCTTTACTAGAATACAAAAATTAGCTGGGTGTGGTGGCGCAC T C DST Ensembl:ENSG00000151914 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1401738676 Functional Loss SNV dbSNP153 33..33 33 - - - 35086 RMVar_ID_35086 Human_SNP_ID_278408063 A-to-I Human chr6 + 57050550 57050550 57050550 GTTGCCCAGGCTGATCTTGAACTTCTGGGCTCAAGTGATCCTCCTGTCTTGGCCTCCCAGTGTGC GTTGCCCAGGCTGATCTTGAACTTCTGGGCTCGAGTGATCCTCCTGTCTTGGCCTCCCAGTGTGC A G KIAA1586 Ensembl:ENSG00000168116 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1016285852 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99233,RMVar_hsa_circ_239141 35087 RMVar_ID_35087 Human_SNP_ID_278409953 A-to-I Human chr6 + 57056747 57056747 57056747 TTTTGTAGAGATGGGGTTTTGCCATGTTGCCCAGGTTGGTATTGGACTCCTGGGCTCAAACAGCC TTTTGTAGAGATGGGGTTTTGCCATGTTGCCCCGGTTGGTATTGGACTCCTGGGCTCAAACAGCC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1011996346 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95106,RMVar_hsa_circ_239144 35088 RMVar_ID_35088 Human_SNP_ID_278410060 A-to-I Human chr6 + 57057129 57057129 57057129 ATGCACCTGTAGTCCCAGCTACTCGGGAGGCTAGGGCAGGAGAATCGCTTGAACACAGGAGGCGG ATGCACCTGTAGTCCCAGCTACTCGGGAGGCTGGGGCAGGAGAATCGCTTGAACACAGGAGGCGG A G - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1298338749 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95106,RMVar_hsa_circ_239144 35089 RMVar_ID_35089 Human_SNP_ID_278410189 A-to-I Human chr6 + 57057660 57057660 57057660 CCTGTAGTCCCAGCTACTCAGGAGGCTGAGACAGGAGAATTGCTTGAACCTGGGAGGCAGAGGTT CCTGTAGTCCCAGCTACTCAGGAGGCTGAGACGGGAGAATTGCTTGAACCTGGGAGGCAGAGGTT A G piR-38580 RNACentral:URS0000251E76 piRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs867941183 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95106,RMVar_hsa_circ_239144 35090 RMVar_ID_35090 Human_SNP_ID_278411255 A-to-I Human chr6 + 57062097 57062097 57062097 AGAACCATAGGCACGTGCCACCACGTTGGGCTAATTTTTGTGTTTTTATAGAGACAGGTTTTCAC AGAACCATAGGCACGTGCCACCACGTTGGGCTGATTTTTGTGTTTTTATAGAGACAGGTTTTCAC A G lnc-KIAA1586-1 RNACentral:URS00008B3648 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs146536634 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95106,RMVar_hsa_circ_239144 35091 RMVar_ID_35091 Human_SNP_ID_278414822 A-to-I Human chr6 + 57077866 57077866 57077866 GATCTCAGCTCACTGCAACCTCCGCGTCTCCCAGGTTCAAGCGATTCTCCTGCCTTAGCCTCCCA GATCTCAGCTCACTGCAACCTCCGCGTCTCCCGGGTTCAAGCGATTCTCCTGCCTTAGCCTCCCA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs773518103 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95106,RMVar_hsa_circ_239144 35092 RMVar_ID_35092 Human_SNP_ID_278414969 A-to-I Human chr6 + 57078699 57078699 57078699 TTCATTAAAATGAGGTCAATATTACTAATCCCAAAACTAGAAAAGGATATCACAAGAAAAGAAAA TTCATTAAAATGAGGTCAATATTACTAATCCCCAAACTAGAAAAGGATATCACAAGAAAAGAAAA A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs921573425 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95106,RMVar_hsa_circ_239144 35093 RMVar_ID_35093 Human_SNP_ID_278414970 A-to-I Human chr6 + 57078699 57078699 57078699 TTCATTAAAATGAGGTCAATATTACTAATCCCAAAACTAGAAAAGGATATCACAAGAAAAGAAAA TTCATTAAAATGAGGTCAATATTACTAATCCCGAAACTAGAAAAGGATATCACAAGAAAAGAAAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs921573425 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95106,RMVar_hsa_circ_239144 35094 RMVar_ID_35094 Human_SNP_ID_278415427 A-to-I Human chr6 + 57080873 57080873 57080873 TGGTGGCATTTGCCTGTAGTCCTAGTGACTCCAGAGACTGAGGTGGGAGGATTGCTTGAGCCCAG TGGTGGCATTTGCCTGTAGTCCTAGTGACTCCCGAGACTGAGGTGGGAGGATTGCTTGAGCCCAG A C - - Other Unknown GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs567628938 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95106,RMVar_hsa_circ_239144 35095 RMVar_ID_35095 Human_SNP_ID_278416536 A-to-I Human chr6 + 57086034 57086034 57086034 ACGATCTCGGCTCACTGCAAGCTTCGCCTCCCAGGTTCATGCCATTCTCCCGCCTCAGCCTCTCT ACGATCTCGGCTCACTGCAAGCTTCGCCTCCCGGGTTCATGCCATTCTCCCGCCTCAGCCTCTCT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs933178115 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95106,RMVar_hsa_circ_239144 35096 RMVar_ID_35096 Human_SNP_ID_278423719 A-to-I Human chr6 + 57115221 57115221 57115221 TCAGGAGGTTGAGGCTTCAGTGAGCTGTGGTCACACCATTGCACTCTAGCCTGGGTAACAAAGTG TCAGGAGGTTGAGGCTTCAGTGAGCTGTGGTCTCACCATTGCACTCTAGCCTGGGTAACAAAGTG A T ZNF451 Ensembl:ENSG00000112200 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs764966477 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15857225 RMVar_hsa_circ_35891,RMVar_hsa_circ_14735,RMVar_hsa_circ_327774,RMVar_hsa_circ_122388,RMVar_hsa_circ_310745,RMVar_hsa_circ_60204,RMVar_hsa_circ_239150,RMVar_hsa_circ_239151,RMVar_hsa_circ_239152 35097 RMVar_ID_35097 Human_SNP_ID_278423724 A-to-I Human chr6 + 57115248 57115247 57115249 TGGTCACACCATTGCACTCTAGCCTGGGTAACAAAGTGAGATCCTGTCAGAAAAAAAAAGTATCT TGGTCACACCATTGCACTCTAGCCTGGGTAAC__AGTGAGATCCTGTCAGAAAAAAAAAGTATCT CAA C ZNF451 Ensembl:ENSG00000112200 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs929729889 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_15857226,Human_RBP_ID_18372550 RMVar_hsa_circ_35891,RMVar_hsa_circ_14735,RMVar_hsa_circ_327774,RMVar_hsa_circ_122388,RMVar_hsa_circ_310745,RMVar_hsa_circ_60204,RMVar_hsa_circ_239150,RMVar_hsa_circ_239151,RMVar_hsa_circ_239152 35098 RMVar_ID_35098 Human_SNP_ID_278424475 A-to-I Human chr6 + 57118512 57118512 57118512 AAATTTAATTTGACCTTTCTCCCCCTTTTTTTAGAAGAGAGTCTTGCTTTGTTGTCCCCCAGGCT AAATTTAATTTGACCTTTCTCCCCCTTTTTTTGGAAGAGAGTCTTGCTTTGTTGTCCCCCAGGCT A G ZNF451 Ensembl:ENSG00000112200 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs940444763 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7619165,Human_RBP_ID_15857317 RMVar_hsa_circ_35891,RMVar_hsa_circ_14735,RMVar_hsa_circ_327774,RMVar_hsa_circ_122388,RMVar_hsa_circ_310745,RMVar_hsa_circ_60204,RMVar_hsa_circ_239150,RMVar_hsa_circ_239151,RMVar_hsa_circ_239152 35099 RMVar_ID_35099 Human_SNP_ID_278424683 A-to-I Human chr6 + 57119404 57119404 57119404 CAAAAATTAGGTGGGTGGTGGCACGCGCCTGCAATCTCAGCTACTCGGGGGCTGAGGCAGGAGAA CAAAAATTAGGTGGGTGGTGGCACGCGCCTGCGATCTCAGCTACTCGGGGGCTGAGGCAGGAGAA A G ZNF451 Ensembl:ENSG00000112200 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1280215979 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35891,RMVar_hsa_circ_14735,RMVar_hsa_circ_327774,RMVar_hsa_circ_122388,RMVar_hsa_circ_310745,RMVar_hsa_circ_60204,RMVar_hsa_circ_239150,RMVar_hsa_circ_239151,RMVar_hsa_circ_239152 35100 RMVar_ID_35100 Human_SNP_ID_278431917 A-to-I Human chr6 - 57151802 57151802 57151802 TAACTTATCCAGGTCAGTATGTTTCTATCTTTAATCCCAATCTTTCTCTTTACATGCTATTTCCT TAACTTATCCAGGTCAGTATGTTTCTATCTTTGATCCCAATCTTTCTCTTTACATGCTATTTCCT T C ZNF451-AS1 Ensembl:ENSG00000226803 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006119323 Functional Loss SNV dbSNP153 33..33 33 - - - 35101 RMVar_ID_35101 Human_SNP_ID_278493341 A-to-I Human chr6 + 57408828 57408828 57408828 TGATCTCCTGGCTCATGGGACCTTCCTGCCTCAACCTCCCAAGTAGCTAGGATTATAGGTGCATA TGATCTCCTGGCTCATGGGACCTTCCTGCCTCGACCTCCCAAGTAGCTAGGATTATAGGTGCATA A G PRIM2 Ensembl:ENSG00000146143 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1192749816 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43753,RMVar_hsa_circ_331015,RMVar_hsa_circ_57631,RMVar_hsa_circ_35114 35102 RMVar_ID_35102 Human_SNP_ID_278583750 A-to-I Human chr6 - 57856459 57856459 57856459 ATAATGCTCCCCTGATGTGGGGAATTAGCTCAAGTGGTAGAGCGCTTGCTTAGCATGCAAGAGGT ATAATGCTCCCCTGATGTGGGGAATTAGCTCATGTGGTAGAGCGCTTGCTTAGCATGCAAGAGGT T A AL021368.3 Ensembl:ENSG00000272541 lincRNA exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs537406950 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23110800,Human_RBP_ID_23112046,Human_RBP_ID_27102643 35103 RMVar_ID_35103 Human_SNP_ID_278583751 A-to-I Human chr6 - 57856459 57856459 57856459 ATAATGCTCCCCTGATGTGGGGAATTAGCTCAAGTGGTAGAGCGCTTGCTTAGCATGCAAGAGGT ATAATGCTCCCCTGATGTGGGGAATTAGCTCAGGTGGTAGAGCGCTTGCTTAGCATGCAAGAGGT T C AL021368.3 Ensembl:ENSG00000272541 lincRNA exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs537406950 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23110800,Human_RBP_ID_23112046,Human_RBP_ID_27102643 35104 RMVar_ID_35104 Human_SNP_ID_278598764 A-to-I Human chr6 - 57921786 57921786 57921786 TTGAGCCCAGGAGTTTGAGATCGGTTTGCACAACATGGACCCCATCTCTACAAAATATTTAAGAT TTGAGCCCAGGAGTTTGAGATCGGTTTGCACACCATGGACCCCATCTCTACAAAATATTTAAGAT T G AL021368.4,GUSBP4 Ensembl:ENSG00000283352,Ensembl:ENSG00000239650 lincRNA,Pseudogene intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs986619501 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_239196,RMVar_hsa_circ_298934 35105 RMVar_ID_35105 Human_SNP_ID_278607232 A-to-I Human chr6 - 57953742 57953742 57953742 AAATTAACCGGGTGTGGGTGGCGGGCACCTGTAGTCCCAGTTACTCGGGAGGCTGAGGCAGGAGA AAATTAACCGGGTGTGGGTGGCGGGCACCTGTCGTCCCAGTTACTCGGGAGGCTGAGGCAGGAGA T G AL021368.4,LINC00680 Ensembl:ENSG00000283352,Ensembl:ENSG00000215190 lincRNA,Pseudogene intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971355659 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113589,RMVar_hsa_circ_239197,RMVar_hsa_circ_239201,RMVar_hsa_circ_99017 35106 RMVar_ID_35106 Human_SNP_ID_278607234 A-to-I Human chr6 - 57953748 57953748 57953748 ATACAAAAATTAACCGGGTGTGGGTGGCGGGCACCTGTAGTCCCAGTTACTCGGGAGGCTGAGGC ATACAAAAATTAACCGGGTGTGGGTGGCGGGCTCCTGTAGTCCCAGTTACTCGGGAGGCTGAGGC T A AL021368.4,LINC00680 Ensembl:ENSG00000283352,Ensembl:ENSG00000215190 lincRNA,Pseudogene intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs977413196 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113589,RMVar_hsa_circ_239197,RMVar_hsa_circ_239201,RMVar_hsa_circ_99017 35107 RMVar_ID_35107 Human_SNP_ID_278607243 A-to-I Human chr6 - 57953778 57953778 57953778 CAACGTGATGAAACCCTGTCTCTACTAAAGATACAAAAATTAACCGGGTGTGGGTGGCGGGCACC CAACGTGATGAAACCCTGTCTCTACTAAAGATGCAAAAATTAACCGGGTGTGGGTGGCGGGCACC T C AL021368.4,LINC00680 Ensembl:ENSG00000283352,Ensembl:ENSG00000215190 lincRNA,Pseudogene intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs936267215 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17422836 RMVar_hsa_circ_113589,RMVar_hsa_circ_239197,RMVar_hsa_circ_239201,RMVar_hsa_circ_99017 35108 RMVar_ID_35108 Human_SNP_ID_518026468 A-to-I Human chr12 - 120095374 120095374 120095374 AGGGGGGTTCCTGGGGGCTTCCAGCCCAGGCTAGAAGCCCCCATGGCTTCTGGCAGCTGGACATC AGGGGGGTTCCTGGGGGCTTCCAGCCCAGGCTGGAAGCCCCCATGGCTTCTGGCAGCTGGACATC T C RAB35 Ensembl:ENSG00000111737 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1344234073 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5111820,Human_RBP_ID_5139722,Human_RBP_ID_8178193,Human_RBP_ID_21884821,Human_RBP_ID_26422715 35109 RMVar_ID_35109 Human_SNP_ID_518026469 A-to-I Human chr12 - 120095374 120095374 120095374 AGGGGGGTTCCTGGGGGCTTCCAGCCCAGGCTAGAAGCCCCCATGGCTTCTGGCAGCTGGACATC AGGGGGGTTCCTGGGGGCTTCCAGCCCAGGCTCGAAGCCCCCATGGCTTCTGGCAGCTGGACATC T G RAB35 Ensembl:ENSG00000111737 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1344234073 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5111820,Human_RBP_ID_5139722,Human_RBP_ID_8178193,Human_RBP_ID_21884821,Human_RBP_ID_26422715 35110 RMVar_ID_35110 Human_SNP_ID_518030524 A-to-I Human chr12 - 120109627 120109627 120109627 AAGCCTGGGCAACGTAGCCAGACTCTGTCCCTACTAAAAATAAAAAAATTAGCTGGGCATGATGG AAGCCTGGGCAACGTAGCCAGACTCTGTCCCTCCTAAAAATAAAAAAATTAGCTGGGCATGATGG T G RAB35 Ensembl:ENSG00000111737 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900783974 Functional Loss SNV dbSNP153 33..33 33 - - - 35111 RMVar_ID_35111 Human_SNP_ID_518031241 A-to-I Human chr12 - 120112141 120112141 120112141 AAACCCTGTCCCTACAAACAATACAAAAAATTAGCTGGGCGTGATGGCGGGCGCCTGTAATCCCA AAACCCTGTCCCTACAAACAATACAAAAAATTTGCTGGGCGTGATGGCGGGCGCCTGTAATCCCA T A RAB35 Ensembl:ENSG00000111737 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1336412138 Functional Loss SNV dbSNP153 33..33 33 - - - 35112 RMVar_ID_35112 Human_SNP_ID_518031242 A-to-I Human chr12 - 120112141 120112141 120112141 AAACCCTGTCCCTACAAACAATACAAAAAATTAGCTGGGCGTGATGGCGGGCGCCTGTAATCCCA AAACCCTGTCCCTACAAACAATACAAAAAATTCGCTGGGCGTGATGGCGGGCGCCTGTAATCCCA T G RAB35 Ensembl:ENSG00000111737 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1336412138 Functional Loss SNV dbSNP153 33..33 33 - - - 35113 RMVar_ID_35113 Human_SNP_ID_518031837 A-to-I Human chr12 - 120114335 120114335 120114335 TAATCCCATCACTTTGGGAGGCCAAGGCGGGCAGATCACCTGAAGACAGGAGTTTGAGACCAACT TAATCCCATCACTTTGGGAGGCCAAGGCGGGCCGATCACCTGAAGACAGGAGTTTGAGACCAACT T G RAB35 Ensembl:ENSG00000111737 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs988994240 Functional Loss SNV dbSNP153 33..33 33 - - - 35114 RMVar_ID_35114 Human_SNP_ID_518043603 A-to-I Human chr12 - 120156915 120156915 120156915 ACTTGGGTGATCGGGACGGGCTCGCCTCGCTTACAGGTGATGTGGTTTTCAGTTGGCTGTTGCTG ACTTGGGTGATCGGGACGGGCTCGCCTCGCTTGCAGGTGATGTGGTTTTCAGTTGGCTGTTGCTG T C GCN1 Ensembl:ENSG00000089154 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs756928985 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8776896,Human_RBP_ID_9279312,Human_RBP_ID_19056924 Human_Splice_Rec_1432320,Human_Splice_Rec_1432321,Human_Splice_Rec_1432393 RMVar_hsa_circ_16258,RMVar_hsa_circ_93383,RMVar_hsa_circ_113123,RMVar_hsa_circ_160658,RMVar_hsa_circ_100597,RMVar_hsa_circ_160672,RMVar_hsa_circ_121438,RMVar_hsa_circ_160659,RMVar_hsa_circ_160660,RMVar_hsa_circ_160667,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_115482,RMVar_hsa_circ_160683,RMVar_hsa_circ_160690,RMVar_hsa_circ_77104,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_160695,RMVar_hsa_circ_160693,RMVar_hsa_circ_160691,RMVar_hsa_circ_11802,RMVar_hsa_circ_25894,RMVar_hsa_circ_121604,RMVar_hsa_circ_86722,RMVar_hsa_circ_102746,RMVar_hsa_circ_36059,RMVar_hsa_circ_6667,RMVar_hsa_circ_98244,RMVar_hsa_circ_160703,RMVar_hsa_circ_160704,RMVar_hsa_circ_160702,RMVar_hsa_circ_23203,RMVar_hsa_circ_121514,RMVar_hsa_circ_127166,RMVar_hsa_circ_104225,RMVar_hsa_circ_160709,RMVar_hsa_circ_160711,RMVar_hsa_circ_67367,RMVar_hsa_circ_160712,RMVar_hsa_circ_160710,RMVar_hsa_circ_112828,RMVar_hsa_circ_160716,RMVar_hsa_circ_362694,RMVar_hsa_circ_85377,RMVar_hsa_circ_91241,RMVar_hsa_circ_80851,RMVar_hsa_circ_10729,RMVar_hsa_circ_160717,RMVar_hsa_circ_160718,RMVar_hsa_circ_160719,RMVar_hsa_circ_73198,RMVar_hsa_circ_101497,RMVar_hsa_circ_160720 35115 RMVar_ID_35115 Human_SNP_ID_518047159 A-to-I Human chr12 - 120169139 120169139 120169139 GGCGCTACGCCGCCACGCGCGGCTAATTTTTTATATTTTTAGTAGAGACAGGGTTTCATCGTGTT GGCGCTACGCCGCCACGCGCGGCTAATTTTTTGTATTTTTAGTAGAGACAGGGTTTCATCGTGTT T C GCN1 Ensembl:ENSG00000089154 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264040770 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116393,RMVar_hsa_circ_160668,RMVar_hsa_circ_117599,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_160691,RMVar_hsa_circ_127166,RMVar_hsa_circ_104225,RMVar_hsa_circ_160709,RMVar_hsa_circ_160710,RMVar_hsa_circ_8132,RMVar_hsa_circ_101497,RMVar_hsa_circ_160720,RMVar_hsa_circ_122941,RMVar_hsa_circ_160723,RMVar_hsa_circ_34195,RMVar_hsa_circ_113969,RMVar_hsa_circ_97493,RMVar_hsa_circ_289890,RMVar_hsa_circ_160725,RMVar_hsa_circ_160727,RMVar_hsa_circ_85130,RMVar_hsa_circ_160726,RMVar_hsa_circ_160733,RMVar_hsa_circ_83082,RMVar_hsa_circ_97869,RMVar_hsa_circ_372494,RMVar_hsa_circ_160732,RMVar_hsa_circ_160735,RMVar_hsa_circ_357486 35116 RMVar_ID_35116 Human_SNP_ID_518047161 A-to-I Human chr12 - 120169146 120169146 120169146 GACTACAGGCGCTACGCCGCCACGCGCGGCTAATTTTTTATATTTTTAGTAGAGACAGGGTTTCA GACTACAGGCGCTACGCCGCCACGCGCGGCTAGTTTTTTATATTTTTAGTAGAGACAGGGTTTCA T C GCN1 Ensembl:ENSG00000089154 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1488390149 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116393,RMVar_hsa_circ_160668,RMVar_hsa_circ_117599,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_160691,RMVar_hsa_circ_127166,RMVar_hsa_circ_104225,RMVar_hsa_circ_160709,RMVar_hsa_circ_160710,RMVar_hsa_circ_8132,RMVar_hsa_circ_101497,RMVar_hsa_circ_160720,RMVar_hsa_circ_122941,RMVar_hsa_circ_160723,RMVar_hsa_circ_34195,RMVar_hsa_circ_113969,RMVar_hsa_circ_97493,RMVar_hsa_circ_289890,RMVar_hsa_circ_160725,RMVar_hsa_circ_160727,RMVar_hsa_circ_85130,RMVar_hsa_circ_160726,RMVar_hsa_circ_160733,RMVar_hsa_circ_83082,RMVar_hsa_circ_97869,RMVar_hsa_circ_372494,RMVar_hsa_circ_160732,RMVar_hsa_circ_160735,RMVar_hsa_circ_357486 35117 RMVar_ID_35117 Human_SNP_ID_518047393 A-to-I Human chr12 - 120169681 120169676 120169682 TGGCCAACATGGTGAAACCCCGTCTTTACTAAAAGTACAAAAATTAGCTGGGTGTGGTGGCGCAT TGGCCAACATGGTGAAACCCCGTCTTTACTA______CAAAAATTAGCTGGGTGTGGTGGCGCAT GTACTTT G GCN1 Ensembl:ENSG00000089154 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs908774884 Functional Loss DEL dbSNP153 32..37 33 - - - Human_RBP_ID_11841280,Human_RBP_ID_22899372 RMVar_hsa_circ_116393,RMVar_hsa_circ_160668,RMVar_hsa_circ_117599,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_160691,RMVar_hsa_circ_127166,RMVar_hsa_circ_104225,RMVar_hsa_circ_160709,RMVar_hsa_circ_160710,RMVar_hsa_circ_8132,RMVar_hsa_circ_101497,RMVar_hsa_circ_160720,RMVar_hsa_circ_122941,RMVar_hsa_circ_160723,RMVar_hsa_circ_34195,RMVar_hsa_circ_113969,RMVar_hsa_circ_97493,RMVar_hsa_circ_289890,RMVar_hsa_circ_160725,RMVar_hsa_circ_160727,RMVar_hsa_circ_85130,RMVar_hsa_circ_160726,RMVar_hsa_circ_160733,RMVar_hsa_circ_83082,RMVar_hsa_circ_97869,RMVar_hsa_circ_372494,RMVar_hsa_circ_160732,RMVar_hsa_circ_160735,RMVar_hsa_circ_357486 35118 RMVar_ID_35118 Human_SNP_ID_518047394 A-to-I Human chr12 - 120169683 120169683 120169683 TCTGGCCAACATGGTGAAACCCCGTCTTTACTAAAAGTACAAAAATTAGCTGGGTGTGGTGGCGC TCTGGCCAACATGGTGAAACCCCGTCTTTACTGAAAGTACAAAAATTAGCTGGGTGTGGTGGCGC T C GCN1 Ensembl:ENSG00000089154 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1259602694 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11841280,Human_RBP_ID_22899372 RMVar_hsa_circ_116393,RMVar_hsa_circ_160668,RMVar_hsa_circ_117599,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_160691,RMVar_hsa_circ_127166,RMVar_hsa_circ_104225,RMVar_hsa_circ_160709,RMVar_hsa_circ_160710,RMVar_hsa_circ_8132,RMVar_hsa_circ_101497,RMVar_hsa_circ_160720,RMVar_hsa_circ_122941,RMVar_hsa_circ_160723,RMVar_hsa_circ_34195,RMVar_hsa_circ_113969,RMVar_hsa_circ_97493,RMVar_hsa_circ_289890,RMVar_hsa_circ_160725,RMVar_hsa_circ_160727,RMVar_hsa_circ_85130,RMVar_hsa_circ_160726,RMVar_hsa_circ_160733,RMVar_hsa_circ_83082,RMVar_hsa_circ_97869,RMVar_hsa_circ_372494,RMVar_hsa_circ_160732,RMVar_hsa_circ_160735,RMVar_hsa_circ_357486 35119 RMVar_ID_35119 Human_SNP_ID_518047400 A-to-I Human chr12 - 120169708 120169708 120169708 CACGAAGTCAAGATTTCGAGACCATTCTGGCCAACATGGTGAAACCCCGTCTTTACTAAAAGTAC CACGAAGTCAAGATTTCGAGACCATTCTGGCCCACATGGTGAAACCCCGTCTTTACTAAAAGTAC T G GCN1 Ensembl:ENSG00000089154 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1247688007 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3395463,Human_RBP_ID_11841281 RMVar_hsa_circ_116393,RMVar_hsa_circ_160668,RMVar_hsa_circ_117599,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_160691,RMVar_hsa_circ_127166,RMVar_hsa_circ_104225,RMVar_hsa_circ_160709,RMVar_hsa_circ_160710,RMVar_hsa_circ_8132,RMVar_hsa_circ_101497,RMVar_hsa_circ_160720,RMVar_hsa_circ_122941,RMVar_hsa_circ_160723,RMVar_hsa_circ_34195,RMVar_hsa_circ_113969,RMVar_hsa_circ_97493,RMVar_hsa_circ_289890,RMVar_hsa_circ_160725,RMVar_hsa_circ_160727,RMVar_hsa_circ_85130,RMVar_hsa_circ_160726,RMVar_hsa_circ_160733,RMVar_hsa_circ_83082,RMVar_hsa_circ_97869,RMVar_hsa_circ_372494,RMVar_hsa_circ_160732,RMVar_hsa_circ_160735,RMVar_hsa_circ_357486 35120 RMVar_ID_35120 Human_SNP_ID_518047725 A-to-I Human chr12 - 120170975 120170975 120170975 CACCCCACCCGGCTAAGACAGGGTTTCACCATATTGGTCAGGCTGGTCTGGAATTCCTGACCTCA CACCCCACCCGGCTAAGACAGGGTTTCACCATGTTGGTCAGGCTGGTCTGGAATTCCTGACCTCA T C GCN1 Ensembl:ENSG00000089154 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs919790415 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117599,RMVar_hsa_circ_160680,RMVar_hsa_circ_160690,RMVar_hsa_circ_123642,RMVar_hsa_circ_56475,RMVar_hsa_circ_104225,RMVar_hsa_circ_160709,RMVar_hsa_circ_8132,RMVar_hsa_circ_101497,RMVar_hsa_circ_160720,RMVar_hsa_circ_113969,RMVar_hsa_circ_97493,RMVar_hsa_circ_289890,RMVar_hsa_circ_160725,RMVar_hsa_circ_160726,RMVar_hsa_circ_97869,RMVar_hsa_circ_160732,RMVar_hsa_circ_304238,RMVar_hsa_circ_357486 35121 RMVar_ID_35121 Human_SNP_ID_518047848 A-to-I Human chr12 - 120171373 120171369 120171373 AACCTCCGCCTCCTGGGTTTAAGCGATTCTCCAACCTCAGCCTCCTGAGTAGCTGGGATTACAGA AACCTCCGCCTCCTGGGTTTAAGCGATTCTCC____TCAGCCTCCTGAGTAGCTGGGATTACAGA AGGTT A GCN1 Ensembl:ENSG00000089154 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1270209328 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_117599,RMVar_hsa_circ_160680,RMVar_hsa_circ_160690,RMVar_hsa_circ_123642,RMVar_hsa_circ_56475,RMVar_hsa_circ_104225,RMVar_hsa_circ_160709,RMVar_hsa_circ_8132,RMVar_hsa_circ_101497,RMVar_hsa_circ_160720,RMVar_hsa_circ_113969,RMVar_hsa_circ_97493,RMVar_hsa_circ_289890,RMVar_hsa_circ_160725,RMVar_hsa_circ_160726,RMVar_hsa_circ_97869,RMVar_hsa_circ_160732,RMVar_hsa_circ_304238,RMVar_hsa_circ_357486 35122 RMVar_ID_35122 Human_SNP_ID_518048304 A-to-I Human chr12 - 120173185 120173185 120173185 GGGCATGGTGGCGGGCACCTGTAATCTCAGCTACGTGGGAGGCTGAGGCAGGGAGAATTGAACCC GGGCATGGTGGCGGGCACCTGTAATCTCAGCTGCGTGGGAGGCTGAGGCAGGGAGAATTGAACCC T C GCN1 Ensembl:ENSG00000089154 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs980554004 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117599,RMVar_hsa_circ_160680,RMVar_hsa_circ_160690,RMVar_hsa_circ_123642,RMVar_hsa_circ_56475,RMVar_hsa_circ_104225,RMVar_hsa_circ_160709,RMVar_hsa_circ_8132,RMVar_hsa_circ_101497,RMVar_hsa_circ_160720,RMVar_hsa_circ_113969,RMVar_hsa_circ_97493,RMVar_hsa_circ_289890,RMVar_hsa_circ_160725,RMVar_hsa_circ_160726,RMVar_hsa_circ_97869,RMVar_hsa_circ_160732,RMVar_hsa_circ_304238,RMVar_hsa_circ_357486 35123 RMVar_ID_35123 Human_SNP_ID_518048306 A-to-I Human chr12 - 120173194 120173194 120173194 AAATTAGCTGGGCATGGTGGCGGGCACCTGTAATCTCAGCTACGTGGGAGGCTGAGGCAGGGAGA AAATTAGCTGGGCATGGTGGCGGGCACCTGTAGTCTCAGCTACGTGGGAGGCTGAGGCAGGGAGA T C GCN1 Ensembl:ENSG00000089154 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs945177665 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117599,RMVar_hsa_circ_160680,RMVar_hsa_circ_160690,RMVar_hsa_circ_123642,RMVar_hsa_circ_56475,RMVar_hsa_circ_104225,RMVar_hsa_circ_160709,RMVar_hsa_circ_8132,RMVar_hsa_circ_101497,RMVar_hsa_circ_160720,RMVar_hsa_circ_113969,RMVar_hsa_circ_97493,RMVar_hsa_circ_289890,RMVar_hsa_circ_160725,RMVar_hsa_circ_160726,RMVar_hsa_circ_97869,RMVar_hsa_circ_160732,RMVar_hsa_circ_304238,RMVar_hsa_circ_357486 35124 RMVar_ID_35124 Human_SNP_ID_518050970 A-to-I Human chr12 - 120182102 120182102 120182102 TTCTGTCACTCAGGTTGGAATGCAGTGGCGCAATCTCGGCTCACTGCAACCTCTGCCTCCCAGGC TTCTGTCACTCAGGTTGGAATGCAGTGGCGCAGTCTCGGCTCACTGCAACCTCTGCCTCCCAGGC T C GCN1 Ensembl:ENSG00000089154 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs903431717 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80413,RMVar_hsa_circ_328382,RMVar_hsa_circ_98601,RMVar_hsa_circ_160738,RMVar_hsa_circ_160740,RMVar_hsa_circ_160739,RMVar_hsa_circ_160743,RMVar_hsa_circ_83250,RMVar_hsa_circ_160746,RMVar_hsa_circ_95142,RMVar_hsa_circ_98067,RMVar_hsa_circ_160748,RMVar_hsa_circ_75848,RMVar_hsa_circ_160747 35125 RMVar_ID_35125 Human_SNP_ID_518051875 A-to-I Human chr12 - 120185661 120185661 120185661 GGGAGGCGGAGGTTGCGGTGAGCCGAGATCGCACTACTGCACTCCAGCCGGGGCGATAGAGTGAG GGGAGGCGGAGGTTGCGGTGAGCCGAGATCGCTCTACTGCACTCCAGCCGGGGCGATAGAGTGAG T A GCN1 Ensembl:ENSG00000089154 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs867041506 Functional Loss SNV dbSNP153 33..33 33 - - - 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 35126 RMVar_ID_35126 Human_SNP_ID_518051876 A-to-I Human chr12 - 120185661 120185661 120185661 GGGAGGCGGAGGTTGCGGTGAGCCGAGATCGCACTACTGCACTCCAGCCGGGGCGATAGAGTGAG GGGAGGCGGAGGTTGCGGTGAGCCGAGATCGCGCTACTGCACTCCAGCCGGGGCGATAGAGTGAG T C GCN1 Ensembl:ENSG00000089154 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs867041506 Functional Loss SNV dbSNP153 33..33 33 - - - 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 35127 RMVar_ID_35127 Human_SNP_ID_518051895 A-to-I Human chr12 - 120185703 120185703 120185703 TCAGCTACTCATGTGGCTGAGGCAGGAGAATCACTTGAACCTGGGAGGCGGAGGTTGCGGTGAGC TCAGCTACTCATGTGGCTGAGGCAGGAGAATCCCTTGAACCTGGGAGGCGGAGGTTGCGGTGAGC T G GCN1 Ensembl:ENSG00000089154 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1301795520 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24938165 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 35128 RMVar_ID_35128 Human_SNP_ID_518052867 A-to-I Human chr12 - 120189197 120189197 120189197 ATGGTGACGCACGCCTGTAATCCTAGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTCAACCTG ATGGTGACGCACGCCTGTAATCCTAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTCAACCTG T C GCN1 Ensembl:ENSG00000089154 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1461536028 Functional Loss SNV dbSNP153 33..33 33 - - - 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 35129 RMVar_ID_35129 Human_SNP_ID_518053040 A-to-I Human chr12 - 120189816 120189816 120189816 CGCCACCACACCCAGCTAATTTTCGTGTTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGC CGCCACCACACCCAGCTAATTTTCGTGTTTTTTGTAGAGATGGGGTTTCACCATGTTGGCCAGGC T A GCN1 Ensembl:ENSG00000089154 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1044722831 Functional Loss SNV dbSNP153 33..33 33 - - - 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 35130 RMVar_ID_35130 Human_SNP_ID_518053041 A-to-I Human chr12 - 120189816 120189816 120189816 CGCCACCACACCCAGCTAATTTTCGTGTTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGC CGCCACCACACCCAGCTAATTTTCGTGTTTTTGGTAGAGATGGGGTTTCACCATGTTGGCCAGGC T C GCN1 Ensembl:ENSG00000089154 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1044722831 Functional Loss SNV dbSNP153 33..33 33 - - - 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 35131 RMVar_ID_35131 Human_SNP_ID_518053057 A-to-I Human chr12 - 120189857 120189857 120189857 CTCATGCCTTAGCCTCTCCAGTAGCTGGGATTACAGGTGTGCGCCACCACACCCAGCTAATTTTC CTCATGCCTTAGCCTCTCCAGTAGCTGGGATTGCAGGTGTGCGCCACCACACCCAGCTAATTTTC T C GCN1 Ensembl:ENSG00000089154 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs938658731 Functional Loss SNV dbSNP153 33..33 33 - - - 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 35132 RMVar_ID_35132 Human_SNP_ID_518053137 A-to-I Human chr12 - 120190186 120190186 120190186 GAGTCTCTCACTGTTGCCCTGGCTGAAGTGCAATGGCACGATCTCAGCTCATTGCAACCTCCACC GAGTCTCTCACTGTTGCCCTGGCTGAAGTGCAGTGGCACGATCTCAGCTCATTGCAACCTCCACC T C GCN1 Ensembl:ENSG00000089154 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1342745529 Functional Loss SNV dbSNP153 33..33 33 - - - 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 35133 RMVar_ID_35133 Human_SNP_ID_518058559 A-to-I Human chr12 + 120207287 120207287 120207287 TGTCGGCCTCGGCCTCCCAAAGTTCTGGGGTTACAGGCATGAGCCACCGTGGCCGGCCGGCAGTT TGTCGGCCTCGGCCTCCCAAAGTTCTGGGGTTGCAGGCATGAGCCACCGTGGCCGGCCGGCAGTT A G PXN-AS1 Ensembl:ENSG00000255857 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs887711987 Functional Loss SNV dbSNP153 33..33 33 - - - 35134 RMVar_ID_35134 Human_SNP_ID_518059123 A-to-I Human chr12 + 120209447 120209447 120209447 TGAGGCATGATAATTGCTTGAACCCAGGAGGTAGAGGCTGCAGTGAACCGAGATCGTGCCACTAC TGAGGCATGATAATTGCTTGAACCCAGGAGGTGGAGGCTGCAGTGAACCGAGATCGTGCCACTAC A G PXN-AS1 Ensembl:ENSG00000255857 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1441987288 Functional Loss SNV dbSNP153 33..33 33 - - - 35135 RMVar_ID_35135 Human_SNP_ID_518059136 A-to-I Human chr12 + 120209478 120209478 120209478 TAGAGGCTGCAGTGAACCGAGATCGTGCCACTACACTCTGGCTTGGATGACAGAGTGAGACTCCA TAGAGGCTGCAGTGAACCGAGATCGTGCCACTGCACTCTGGCTTGGATGACAGAGTGAGACTCCA A G PXN-AS1 Ensembl:ENSG00000255857 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1240976416 Functional Loss SNV dbSNP153 33..33 33 - - - 35136 RMVar_ID_35136 Human_SNP_ID_518069399 A-to-I Human chr12 - 120248878 120248878 120248878 CCCGCCTCAGCCTCCCAAAGTTTTGGGATTACAGACGTGAACCACTGCACCTGGCCATAACTGCC CCCGCCTCAGCCTCCCAAAGTTTTGGGATTACGGACGTGAACCACTGCACCTGGCCATAACTGCC T C PXN Ensembl:ENSG00000089159 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs963174422 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11841903 35137 RMVar_ID_35137 Human_SNP_ID_518080520 A-to-I Human chr12 - 120291302 120291302 120291302 CGGCTGACTGCAACCTCCACATTCCGGGTTCAAGCGATTCTCTGTCTCAGCCTCCGGAGTAGCTG CGGCTGACTGCAACCTCCACATTCCGGGTTCAGGCGATTCTCTGTCTCAGCCTCCGGAGTAGCTG T C RF00017-049,RF00017-1304,lnc-PLA2G1B-2 RNACentral:URS000096B6E3,RNACentral:URS0000990DE9,RNACentral:URS0000D58AC8 SRP RNA,SRP RNA,lincRNA intron,intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs549990185 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6141995,Human_RBP_ID_11841975 35138 RMVar_ID_35138 Human_SNP_ID_518121605 A-to-I Human chr12 + 120441119 120441118 120441119 CCGGGCCAACATGATGAAATCCTGTCTCTACTAAAAATACAAAAATTAGTTGGGTGTGGTGGCGC CCGGGCCAACATGATGAAATCCTGTCTCTACT_AAAATACAAAAATTAGTTGGGTGTGGTGGCGC TA T AL021546.1 Ensembl:ENSG00000111780 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1565910076 Functional Loss DEL dbSNP153 33..33 33 - - - 35139 RMVar_ID_35139 Human_SNP_ID_518123543 A-to-I Human chr12 + 120447336 120447334 120447336 CCTGACCGTGATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCGC CCTGACCGTGATCCACCCGCCTCGGCCTCCC__AGTGCTGGGATTACAGGTGTGAGCCACCGCGC CAA C GATC,AL021546.1 Ensembl:ENSG00000257218,Ensembl:ENSG00000111780 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1182728073 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_107284,RMVar_hsa_circ_160782 35140 RMVar_ID_35140 Human_SNP_ID_518124201 A-to-I Human chr12 + 120449631 120449630 120449632 CACCATGCCTGGTTAATTTTTGTATTTTTAGTAGAGAGGGGTTTCACCATGTTGGCAAGGCTCGT CACCATGCCTGGTTAATTTTTGTATTTTTAGT__AGAGGGGTTTCACCATGTTGGCAAGGCTCGT TAG T GATC,AL021546.1 Ensembl:ENSG00000257218,Ensembl:ENSG00000111780 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1344031499 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_107284,RMVar_hsa_circ_160782 35141 RMVar_ID_35141 Human_SNP_ID_518124494 A-to-I Human chr12 + 120450870 120450870 120450870 TTAGCTATAAAAGCCCTGACTTGGCCGGGCATAATGGCTCACTCCTGTAATCCCAGCATTTTGGG TTAGCTATAAAAGCCCTGACTTGGCCGGGCATGATGGCTCACTCCTGTAATCCCAGCATTTTGGG A G GATC,AL021546.1 Ensembl:ENSG00000257218,Ensembl:ENSG00000111780 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs781500946 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107284,RMVar_hsa_circ_160782 35142 RMVar_ID_35142 Human_SNP_ID_518125262 A-to-I Human chr12 + 120453791 120453791 120453791 ATCACTTGAGCCCAGAAGTTTGAGACCAGCCTAGGCAACACAGCAAGACCCTGTCTCAAAAAAAA ATCACTTGAGCCCAGAAGTTTGAGACCAGCCTGGGCAACACAGCAAGACCCTGTCTCAAAAAAAA A G GATC,AL021546.1 Ensembl:ENSG00000257218,Ensembl:ENSG00000111780 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1012193666 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107284,RMVar_hsa_circ_160782 35143 RMVar_ID_35143 Human_SNP_ID_518127183 A-to-I Human chr12 + 120460459 120460459 120460459 CTTTCTTCCCAGAAGAGGGCTAACTTCCTACTAAGGTCTGAAGAGTGTTGAAAGTAGACTAGAGC CTTTCTTCCCAGAAGAGGGCTAACTTCCTACTGAGGTCTGAAGAGTGTTGAAAGTAGACTAGAGC A G GATC Ensembl:ENSG00000257218 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1447956478 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_990047,Human_RBP_ID_1788695,Human_RBP_ID_4205167,Human_RBP_ID_8066090,Human_RBP_ID_8178204,Human_RBP_ID_11842783,Human_RBP_ID_18256077,Human_RBP_ID_23542096,Human_RBP_ID_26412702,Human_RBP_ID_27623693 35144 RMVar_ID_35144 Human_SNP_ID_518127186 A-to-I Human chr12 + 120460482 120460482 120460482 CTTCCTACTAAGGTCTGAAGAGTGTTGAAAGTAGACTAGAGCTTGGGAACTCCTAACCTAGAACT CTTCCTACTAAGGTCTGAAGAGTGTTGAAAGTTGACTAGAGCTTGGGAACTCCTAACCTAGAACT A T GATC Ensembl:ENSG00000257218 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs141488114 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1788695,Human_RBP_ID_8179424,Human_RBP_ID_11842783,Human_RBP_ID_18256077,Human_RBP_ID_23542096,Human_RBP_ID_26412702 35145 RMVar_ID_35145 Human_SNP_ID_518127187 A-to-I Human chr12 + 120460497 120460496 120460497 TGAAGAGTGTTGAAAGTAGACTAGAGCTTGGGAACTCCTAACCTAGAACTATCTGCCATCCCACA TGAAGAGTGTTGAAAGTAGACTAGAGCTTGGG_ACTCCTAACCTAGAACTATCTGCCATCCCACA GA G GATC Ensembl:ENSG00000257218 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1480267255 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_1788695,Human_RBP_ID_8179424,Human_RBP_ID_11842783,Human_RBP_ID_26412702 35146 RMVar_ID_35146 Human_SNP_ID_518127188 A-to-I Human chr12 + 120460497 120460497 120460497 TGAAGAGTGTTGAAAGTAGACTAGAGCTTGGGAACTCCTAACCTAGAACTATCTGCCATCCCACA TGAAGAGTGTTGAAAGTAGACTAGAGCTTGGGCACTCCTAACCTAGAACTATCTGCCATCCCACA A C GATC Ensembl:ENSG00000257218 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1362663603 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1788695,Human_RBP_ID_8179424,Human_RBP_ID_11842783,Human_RBP_ID_26412702 35147 RMVar_ID_35147 Human_SNP_ID_518127245 A-to-I Human chr12 + 120460750 120460750 120460750 AAAGTGGGCTGGGCGCAGTGGCTCACTCCTGTAATCCCAGCACTTTGGGAGGCTGAGACGGGCGG AAAGTGGGCTGGGCGCAGTGGCTCACTCCTGTGATCCCAGCACTTTGGGAGGCTGAGACGGGCGG A G GATC Ensembl:ENSG00000257218 Protein coding 3'UTR GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-Seq:(High) rs3205956 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26421744 35148 RMVar_ID_35148 Human_SNP_ID_518127277 A-to-I Human chr12 + 120460842 120460841 120460843 CCTGGCTAATGCGGTGAAACCTCATCTCTACTAAAAATACAAAAAATTAGCTGGGTGTGATGACA CCTGGCTAATGCGGTGAAACCTCATCTCTACT__AAATACAAAAAATTAGCTGGGTGTGATGACA TAA T GATC Ensembl:ENSG00000257218 Protein coding 3'UTR GSE47997;GSE100210;GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;HepG2 cell line;HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,29129909,29129909,32596459 RNA-Seq:(High) rs961064926 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_26412713 35149 RMVar_ID_35149 Human_SNP_ID_518127395 A-to-I Human chr12 + 120461213 120461213 120461213 CAACTCCTGGGCTCAAGTGATCCTCCCACCTCAGCCTCCTAAGTAACTGGGACTACATATGTGCA CAACTCCTGGGCTCAAGTGATCCTCCCACCTCCGCCTCCTAAGTAACTGGGACTACATATGTGCA A C GATC Ensembl:ENSG00000257218 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs117232182 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_582613,Human_miRNA_ID_1128690 35150 RMVar_ID_35150 Human_SNP_ID_518127396 A-to-I Human chr12 + 120461213 120461213 120461213 CAACTCCTGGGCTCAAGTGATCCTCCCACCTCAGCCTCCTAAGTAACTGGGACTACATATGTGCA CAACTCCTGGGCTCAAGTGATCCTCCCACCTCGGCCTCCTAAGTAACTGGGACTACATATGTGCA A G GATC Ensembl:ENSG00000257218 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs117232182 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_582613,Human_miRNA_ID_1128690 35151 RMVar_ID_35151 Human_SNP_ID_518129064 A-to-I Human chr12 - 120467884 120467884 120467884 CTCCATGTTGGCCAGGTTTGTCTTGAACTCCTAACCTCAAGTGATCCACCCACCTCAGCCTCCCA CTCCATGTTGGCCAGGTTTGTCTTGAACTCCTGACCTCAAGTGATCCACCCACCTCAGCCTCCCA T C SRSF9 Ensembl:ENSG00000111786 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1255530118 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11843158 35152 RMVar_ID_35152 Human_SNP_ID_518130924 A-to-I Human chr12 + 120474135 120474135 120474135 CAGCCTGGGCAACATGTTAAAACCCCGTCTCTACAAAAAATACAAAAATTAGCTGGGCATGGTGG CAGCCTGGGCAACATGTTAAAACCCCGTCTCTGCAAAAAATACAAAAATTAGCTGGGCATGGTGG A G DYNLL1 Ensembl:ENSG00000088986 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1342858279 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88195,RMVar_hsa_circ_160785 35153 RMVar_ID_35153 Human_SNP_ID_518133502 A-to-I Human chr12 - 120484868 120484868 120484868 CAGGTGTAGTGTTGCGTGCCTGTAGGCTACTTAGGAGGCTGAGGCAGGAGAATCGCTTGAACCCA CAGGTGTAGTGTTGCGTGCCTGTAGGCTACTTCGGAGGCTGAGGCAGGAGAATCGCTTGAACCCA T G NRAV,NRAV:2,NRAV:3 RNACentral:URS0000D5CED7,RNACentral:URS0000D5CDA0,RNACentral:URS0000D58B6E lincRNA,lincRNA,lincRNA exon,exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1161727549 Functional Loss SNV dbSNP153 33..33 33 - - - 35154 RMVar_ID_35154 Human_SNP_ID_518133533 A-to-I Human chr12 - 120485021 120485021 120485021 TTTATAGCCCATGCGGCCAGGGGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCCAG TTTATAGCCCATGCGGCCAGGGGCGGTGGCTCCCGCCTGTAATCCCAGCACTTTGGGAGGCCCAG T G NRAV,NRAV:2,NRAV:3 RNACentral:URS0000D5CED7,RNACentral:URS0000D5CDA0,RNACentral:URS0000D58B6E lincRNA,lincRNA,lincRNA exon,exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1022238922 Functional Loss SNV dbSNP153 33..33 33 - - - 35155 RMVar_ID_35155 Human_SNP_ID_518133740 A-to-I Human chr12 - 120485781 120485781 120485781 GCTAGGGTGTAGTGGTGCGATCGTACCTCACTACAGCCTCAAACTCCCAGGCTCAAGGGATCCGA GCTAGGGTGTAGTGGTGCGATCGTACCTCACTGCAGCCTCAAACTCCCAGGCTCAAGGGATCCGA T C NRAV,NRAV:2,NRAV:3 RNACentral:URS0000D5CED7,RNACentral:URS0000D5CDA0,RNACentral:URS0000D58B6E lincRNA,lincRNA,lincRNA intron,exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1458473830 Functional Loss SNV dbSNP153 33..33 33 - - - 35156 RMVar_ID_35156 Human_SNP_ID_518134081 A-to-I Human chr12 - 120487113 120487113 120487113 AAAATTAGCCGGGTGTGGTGGCGGGCGCCTGTAGTCCCAGCTACTAGGGAGGCTGAAGCAGGACA AAAATTAGCCGGGTGTGGTGGCGGGCGCCTGTCGTCCCAGCTACTAGGGAGGCTGAAGCAGGACA T G NRAV,NRAV:2,NRAV:3 RNACentral:URS0000D5CED7,RNACentral:URS0000D5CDA0,RNACentral:URS0000D58B6E lincRNA,lincRNA,lincRNA exon,exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1296035697 Functional Loss SNV dbSNP153 33..33 33 - - - 35157 RMVar_ID_35157 Human_SNP_ID_518134364 A-to-I Human chr12 + 120488160 120488160 120488160 GCCGCAGAAGACAGTCCACGTGTCTTAACCAGACTTACAAGACTCCAAAGGTCTGGCTTCTCCCC GCCGCAGAAGACAGTCCACGTGTCTTAACCAGGCTTACAAGACTCCAAAGGTCTGGCTTCTCCCC A G DYNLL1 Ensembl:ENSG00000088986 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs615298 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1433112,Human_Splice_Rec_1433113,Human_Splice_Rec_1433122,Human_Splice_Rec_1433123 RMVar_hsa_circ_88195,RMVar_hsa_circ_74645,RMVar_hsa_circ_160785 35158 RMVar_ID_35158 Human_SNP_ID_518134534 A-to-I Human chr12 - 120488942 120488942 120488942 CCTTGAGTTCCTACCCTGTCTTTTAGTCACTTAGTCCTTTTTTTCTCTTTTTTCTTTTTTTGAGA CCTTGAGTTCCTACCCTGTCTTTTAGTCACTTGGTCCTTTTTTTCTCTTTTTTCTTTTTTTGAGA T C NRAV Ensembl:ENSG00000248008 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs977063741 Functional Loss SNV dbSNP153 33..33 33 - - - 35159 RMVar_ID_35159 Human_SNP_ID_518142134 A-to-I Human chr12 - 120518792 120518792 120518792 TTGGGAGGCTGAGGCGTGTGGATCACGAGGTCAGGAGTCTGAGACCAGCCTGACCAATGTGGTGA TTGGGAGGCTGAGGCGTGTGGATCACGAGGTCGGGAGTCTGAGACCAGCCTGACCAATGTGGTGA T C COQ5 Ensembl:ENSG00000110871 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs916389577 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50414,RMVar_hsa_circ_160792,RMVar_hsa_circ_370482,RMVar_hsa_circ_294736,RMVar_hsa_circ_160795,RMVar_hsa_circ_334346,RMVar_hsa_circ_160796 35160 RMVar_ID_35160 Human_SNP_ID_518142780 A-to-I Human chr12 - 120521195 120521195 120521195 CAGTGTGGTAGCTGGTGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATTGCTTGAA CAGTGTGGTAGCTGGTGCCTGTAATCCCAGCTGCTTGGGAGGCTGAGGCAGGAGAATTGCTTGAA T C COQ5 Ensembl:ENSG00000110871 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs958170678 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50414,RMVar_hsa_circ_160792,RMVar_hsa_circ_370482,RMVar_hsa_circ_294736,RMVar_hsa_circ_160795,RMVar_hsa_circ_334346,RMVar_hsa_circ_160796 35161 RMVar_ID_35161 Human_SNP_ID_518142882 A-to-I Human chr12 - 120521564 120521564 120521564 TTCAAGCAATTCTCTGCCTCAGCCTCCTGAGTAGCTGGGATTATAGGCATGCACCACCACGCCTG TTCAAGCAATTCTCTGCCTCAGCCTCCTGAGTGGCTGGGATTATAGGCATGCACCACCACGCCTG T C COQ5 Ensembl:ENSG00000110871 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs527475778 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50414,RMVar_hsa_circ_160792,RMVar_hsa_circ_370482,RMVar_hsa_circ_294736,RMVar_hsa_circ_160795,RMVar_hsa_circ_334346,RMVar_hsa_circ_160796 35162 RMVar_ID_35162 Human_SNP_ID_518142888 A-to-I Human chr12 - 120521588 120521588 120521588 CCACTGCAACCTCCACCTCCGGGGTTCAAGCAATTCTCTGCCTCAGCCTCCTGAGTAGCTGGGAT CCACTGCAACCTCCACCTCCGGGGTTCAAGCAGTTCTCTGCCTCAGCCTCCTGAGTAGCTGGGAT T C COQ5 Ensembl:ENSG00000110871 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs905796264 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50414,RMVar_hsa_circ_160792,RMVar_hsa_circ_370482,RMVar_hsa_circ_294736,RMVar_hsa_circ_160795,RMVar_hsa_circ_334346,RMVar_hsa_circ_160796 35163 RMVar_ID_35163 Human_SNP_ID_518143444 A-to-I Human chr12 - 120523261 120523261 120523261 GCCATCTCGGCTCACTGCAAGCTCCACCTCCCAGGTTCACGCCATTCTCCTGCCTCAGCCTCCCG GCCATCTCGGCTCACTGCAAGCTCCACCTCCCGGGTTCACGCCATTCTCCTGCCTCAGCCTCCCG T C COQ5,RPL29P24 Ensembl:ENSG00000110871,Ensembl:ENSG00000241030 Protein coding,Pseudogene intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs866899065 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50414 35164 RMVar_ID_35164 Human_SNP_ID_518143580 A-to-I Human chr12 - 120523838 120523838 120523838 GCCCAGCTAATTTTTGTGTTTTTACTAGAGACAGGGTTTTGCCATGTTGGCCAGGCTAGCCTTGA GCCCAGCTAATTTTTGTGTTTTTACTAGAGACGGGGTTTTGCCATGTTGGCCAGGCTAGCCTTGA T C COQ5 Ensembl:ENSG00000110871 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1387974201 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50414 35165 RMVar_ID_35165 Human_SNP_ID_518143599 A-to-I Human chr12 - 120523909 120523909 120523909 ACCTTCCAGGTTCCAGTGATTCTCCTGCCCCAACCACCCGAGTAGCTGGGATTACAGGTGTGCAC ACCTTCCAGGTTCCAGTGATTCTCCTGCCCCAGCCACCCGAGTAGCTGGGATTACAGGTGTGCAC T C COQ5 Ensembl:ENSG00000110871 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1462373130 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1433202,Human_Splice_Rec_1433203 RMVar_hsa_circ_50414 35166 RMVar_ID_35166 Human_SNP_ID_518143620 A-to-I Human chr12 - 120523958 120523958 120523958 TCGCCCAGGCTGGAATGCAGTGGTCCAATTTCAGCTCACTGCAACCTCTACCTTCCAGGTTCCAG TCGCCCAGGCTGGAATGCAGTGGTCCAATTTCGGCTCACTGCAACCTCTACCTTCCAGGTTCCAG T C COQ5 Ensembl:ENSG00000110871 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1243400423 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1433202,Human_Splice_Rec_1433203 RMVar_hsa_circ_50414 35167 RMVar_ID_35167 Human_SNP_ID_518143632 A-to-I Human chr12 - 120523976 120523976 120523976 AAACAGAGTCTCTCTCTGTCGCCCAGGCTGGAATGCAGTGGTCCAATTTCAGCTCACTGCAACCT AAACAGAGTCTCTCTCTGTCGCCCAGGCTGGAGTGCAGTGGTCCAATTTCAGCTCACTGCAACCT T C COQ5 Ensembl:ENSG00000110871 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1455792836 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1433202,Human_Splice_Rec_1433203 RMVar_hsa_circ_50414 35168 RMVar_ID_35168 Human_SNP_ID_518143649 A-to-I Human chr12 - 120524004 120524004 120524004 TAATCATGCATCTTTCATCTTTATTTTGAAACAGAGTCTCTCTCTGTCGCCCAGGCTGGAATGCA TAATCATGCATCTTTCATCTTTATTTTGAAACGGAGTCTCTCTCTGTCGCCCAGGCTGGAATGCA T C COQ5 Ensembl:ENSG00000110871 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1259777611 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50414 35169 RMVar_ID_35169 Human_SNP_ID_518143650 A-to-I Human chr12 - 120524007 120524007 120524007 CATTAATCATGCATCTTTCATCTTTATTTTGAAACAGAGTCTCTCTCTGTCGCCCAGGCTGGAAT CATTAATCATGCATCTTTCATCTTTATTTTGAGACAGAGTCTCTCTCTGTCGCCCAGGCTGGAAT T C COQ5 Ensembl:ENSG00000110871 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1486094206 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50414 35170 RMVar_ID_35170 Human_SNP_ID_518144124 A-to-I Human chr12 - 120525662 120525662 120525662 CCTCAGCCTCCCAAAGTTCTGGGATTATAGGCATGAGCCACTGCGCCCAGCCTTGTTTATTTATT CCTCAGCCTCCCAAAGTTCTGGGATTATAGGCGTGAGCCACTGCGCCCAGCCTTGTTTATTTATT T C COQ5 Ensembl:ENSG00000110871 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1286347174 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50414 35171 RMVar_ID_35171 Human_SNP_ID_518144149 A-to-I Human chr12 - 120525735 120525735 120525735 TATTTTTAGTAGAGATGGAGTTTCACTGTGTTAGCTAGGATGGTCTCGATCTCTGGACCTCGTGA TATTTTTAGTAGAGATGGAGTTTCACTGTGTTGGCTAGGATGGTCTCGATCTCTGGACCTCGTGA T C COQ5 Ensembl:ENSG00000110871 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs544827528 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50414 35172 RMVar_ID_35172 Human_SNP_ID_518144644 A-to-I Human chr12 - 120527243 120527243 120527243 CATCTCTACTAAAAATACAAAAAAAATTAGCCAAGCATGGTGACGCACGCCTGTAATCACAGCTA CATCTCTACTAAAAATACAAAAAAAATTAGCCGAGCATGGTGACGCACGCCTGTAATCACAGCTA T C COQ5 Ensembl:ENSG00000110871 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs188620240 Functional Loss SNV dbSNP153 33..33 33 - - - 35173 RMVar_ID_35173 Human_SNP_ID_518144645 A-to-I Human chr12 - 120527243 120527243 120527243 CATCTCTACTAAAAATACAAAAAAAATTAGCCAAGCATGGTGACGCACGCCTGTAATCACAGCTA CATCTCTACTAAAAATACAAAAAAAATTAGCCCAGCATGGTGACGCACGCCTGTAATCACAGCTA T G COQ5 Ensembl:ENSG00000110871 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs188620240 Functional Loss SNV dbSNP153 33..33 33 - - - 35174 RMVar_ID_35174 Human_SNP_ID_518144663 A-to-I Human chr12 - 120527289 120527289 120527289 TTGAAGTCAGGAGTTCGAGACCAGCCTGGCCAACGTGGTGAAACCTCATCTCTACTAAAAATACA TTGAAGTCAGGAGTTCGAGACCAGCCTGGCCAGCGTGGTGAAACCTCATCTCTACTAAAAATACA T C COQ5 Ensembl:ENSG00000110871 Protein coding intron GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs1178199893 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1433206 35175 RMVar_ID_35175 Human_SNP_ID_518144839 A-to-I Human chr12 - 120527953 120527953 120527953 ACTGAGTCTCTCTCTGTCACCCCCAGGCTGGAAGGCAGTGGCGCGATCTCGGCTCACTGCAAGCT ACTGAGTCTCTCTCTGTCACCCCCAGGCTGGAGGGCAGTGGCGCGATCTCGGCTCACTGCAAGCT T C COQ5 Ensembl:ENSG00000110871 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202322071 Functional Loss SNV dbSNP153 33..33 33 - - - 35176 RMVar_ID_35176 Human_SNP_ID_518144939 A-to-I Human chr12 - 120528080 120528080 120528080 CTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCATCTGCCACTGTGCCCTGCTAATTTTT CTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTGCAGGCATCTGCCACTGTGCCCTGCTAATTTTT T C COQ5 Ensembl:ENSG00000110871 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1259634715 Functional Loss SNV dbSNP153 33..33 33 - - - 35177 RMVar_ID_35177 Human_SNP_ID_518145092 A-to-I Human chr12 - 120528656 120528656 120528656 GGGATTACAGGCGCCCGCCAGCACGCCCGGCTAACTTTTTTGTATTCTTACTAGAGATGGGGTTT GGGATTACAGGCGCCCGCCAGCACGCCCGGCTGACTTTTTTGTATTCTTACTAGAGATGGGGTTT T C COQ5 Ensembl:ENSG00000110871 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1429366751 Functional Loss SNV dbSNP153 33..33 33 - - - 35178 RMVar_ID_35178 Human_SNP_ID_518149417 A-to-I Human chr12 + 120544400 120544400 120544400 AAAAAATTGGCTGGGAGTGTTGGCTCATGCCTATAATACCAGCACTTTGGGAGGCCGAGCAGATG AAAAAATTGGCTGGGAGTGTTGGCTCATGCCTGTAATACCAGCACTTTGGGAGGCCGAGCAGATG A G RNF10 Ensembl:ENSG00000022840 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1445708123 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24938720 RMVar_hsa_circ_16657,RMVar_hsa_circ_106714,RMVar_hsa_circ_160797,RMVar_hsa_circ_295150,RMVar_hsa_circ_311176,RMVar_hsa_circ_160798,RMVar_hsa_circ_160799 35179 RMVar_ID_35179 Human_SNP_ID_518149447 A-to-I Human chr12 + 120544536 120544536 120544536 AAAATCAGCTGGACATGGTGGTGAGTGCCTGTAGTCTCAGCTGCTCAGGAGGCTGAAGTGGGAGG AAAATCAGCTGGACATGGTGGTGAGTGCCTGTGGTCTCAGCTGCTCAGGAGGCTGAAGTGGGAGG A G RNF10 Ensembl:ENSG00000022840 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1429925797 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16657,RMVar_hsa_circ_106714,RMVar_hsa_circ_160797,RMVar_hsa_circ_295150,RMVar_hsa_circ_311176,RMVar_hsa_circ_160798,RMVar_hsa_circ_160799 35180 RMVar_ID_35180 Human_SNP_ID_518149451 A-to-I Human chr12 + 120544550 120544550 120544550 ATGGTGGTGAGTGCCTGTAGTCTCAGCTGCTCAGGAGGCTGAAGTGGGAGGGTGGCTTGAGCCTG ATGGTGGTGAGTGCCTGTAGTCTCAGCTGCTCGGGAGGCTGAAGTGGGAGGGTGGCTTGAGCCTG A G RNF10 Ensembl:ENSG00000022840 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1243972662 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16657,RMVar_hsa_circ_106714,RMVar_hsa_circ_160797,RMVar_hsa_circ_295150,RMVar_hsa_circ_311176,RMVar_hsa_circ_160798,RMVar_hsa_circ_160799 35181 RMVar_ID_35181 Human_SNP_ID_518150756 A-to-I Human chr12 + 120549598 120549598 120549598 CCTGAGGCCAGGAGTTTGAGACGGGCCTGGCTAATGTGGCAAAACTCTGTCTCTACTAAAAATAC CCTGAGGCCAGGAGTTTGAGACGGGCCTGGCTGATGTGGCAAAACTCTGTCTCTACTAAAAATAC A G RNF10 Ensembl:ENSG00000022840 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1366517854 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_53195,RMVar_hsa_circ_16657,RMVar_hsa_circ_106714,RMVar_hsa_circ_160797,RMVar_hsa_circ_295150,RMVar_hsa_circ_160799,RMVar_hsa_circ_265128,RMVar_hsa_circ_355918,RMVar_hsa_circ_68570,RMVar_hsa_circ_34227,RMVar_hsa_circ_160801 35182 RMVar_ID_35182 Human_SNP_ID_518152586 A-to-I Human chr12 + 120555617 120555617 120555617 TCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAACTGGGACTACAGGCACGCACCACCACTCCCA TCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTGACTGGGACTACAGGCACGCACCACCACTCCCA A G RNF10 Ensembl:ENSG00000022840 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1444556940 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106714,RMVar_hsa_circ_160797,RMVar_hsa_circ_295150,RMVar_hsa_circ_160799,RMVar_hsa_circ_265128,RMVar_hsa_circ_68570,RMVar_hsa_circ_88407,RMVar_hsa_circ_34227,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_311391,RMVar_hsa_circ_323851,RMVar_hsa_circ_332619,RMVar_hsa_circ_307791,RMVar_hsa_circ_290831,RMVar_hsa_circ_294043,RMVar_hsa_circ_27491,RMVar_hsa_circ_160807,RMVar_hsa_circ_160809,RMVar_hsa_circ_160810,RMVar_hsa_circ_160808,RMVar_hsa_circ_160806 35183 RMVar_ID_35183 Human_SNP_ID_518152609 A-to-I Human chr12 + 120555676 120555676 120555676 CTCCCAGCTAATTTTTTTTTGTATTTTTTTTTAGTAGAGATGGGGTTTCTCCATGTTGGTCAGGC CTCCCAGCTAATTTTTTTTTGTATTTTTTTTTGGTAGAGATGGGGTTTCTCCATGTTGGTCAGGC A G RNF10 Ensembl:ENSG00000022840 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1344072478 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24938770 RMVar_hsa_circ_106714,RMVar_hsa_circ_160797,RMVar_hsa_circ_295150,RMVar_hsa_circ_160799,RMVar_hsa_circ_265128,RMVar_hsa_circ_68570,RMVar_hsa_circ_88407,RMVar_hsa_circ_34227,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_311391,RMVar_hsa_circ_323851,RMVar_hsa_circ_332619,RMVar_hsa_circ_307791,RMVar_hsa_circ_290831,RMVar_hsa_circ_294043,RMVar_hsa_circ_27491,RMVar_hsa_circ_160807,RMVar_hsa_circ_160809,RMVar_hsa_circ_160810,RMVar_hsa_circ_160808,RMVar_hsa_circ_160806 35184 RMVar_ID_35184 Human_SNP_ID_518156313 A-to-I Human chr12 + 120568111 120568111 120568111 TACAAAAAATACGAAATTTAGCCAGGTGTGGTAGTGTGTACCTGTAGTCCCAGCTACTTGGGAGG TACAAAAAATACGAAATTTAGCCAGGTGTGGTGGTGTGTACCTGTAGTCCCAGCTACTTGGGAGG A G RNF10 Ensembl:ENSG00000022840 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1368103340 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88407,RMVar_hsa_circ_86391,RMVar_hsa_circ_160802,RMVar_hsa_circ_160803,RMVar_hsa_circ_307791,RMVar_hsa_circ_27491,RMVar_hsa_circ_160816,RMVar_hsa_circ_327844,RMVar_hsa_circ_160810,RMVar_hsa_circ_375920,RMVar_hsa_circ_160815,RMVar_hsa_circ_37149,RMVar_hsa_circ_83786,RMVar_hsa_circ_160817,RMVar_hsa_circ_84745,RMVar_hsa_circ_88087,RMVar_hsa_circ_16332,RMVar_hsa_circ_160825,RMVar_hsa_circ_160828,RMVar_hsa_circ_309102,RMVar_hsa_circ_160826,RMVar_hsa_circ_376353,RMVar_hsa_circ_160829,RMVar_hsa_circ_122660,RMVar_hsa_circ_286489,RMVar_hsa_circ_106013,RMVar_hsa_circ_160830,RMVar_hsa_circ_160831,RMVar_hsa_circ_160832 35185 RMVar_ID_35185 Human_SNP_ID_518156580 A-to-I Human chr12 + 120569169 120569169 120569169 TTTTGTATTTTTAGTAGAGACAGGGTTTCTCCATGTTGGTCAGGCTAGTCTCAAACTCCTGACCT TTTTGTATTTTTAGTAGAGACAGGGTTTCTCCCTGTTGGTCAGGCTAGTCTCAAACTCCTGACCT A C RNF10 Ensembl:ENSG00000022840 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs970398071 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88407,RMVar_hsa_circ_86391,RMVar_hsa_circ_160802,RMVar_hsa_circ_160803,RMVar_hsa_circ_307791,RMVar_hsa_circ_27491,RMVar_hsa_circ_160816,RMVar_hsa_circ_327844,RMVar_hsa_circ_160810,RMVar_hsa_circ_375920,RMVar_hsa_circ_160815,RMVar_hsa_circ_37149,RMVar_hsa_circ_83786,RMVar_hsa_circ_160817,RMVar_hsa_circ_84745,RMVar_hsa_circ_88087,RMVar_hsa_circ_16332,RMVar_hsa_circ_160825,RMVar_hsa_circ_160828,RMVar_hsa_circ_309102,RMVar_hsa_circ_160826,RMVar_hsa_circ_376353,RMVar_hsa_circ_160829,RMVar_hsa_circ_122660,RMVar_hsa_circ_286489,RMVar_hsa_circ_106013,RMVar_hsa_circ_160830,RMVar_hsa_circ_160831,RMVar_hsa_circ_160832 35186 RMVar_ID_35186 Human_SNP_ID_518156836 A-to-I Human chr12 + 120569992 120569992 120569992 TTGGCTCACTGCAACTTCCCCCTCGCGGGTTCAAGCGATTCTCCTGCCCCAGCCTCCTGAGTAGC TTGGCTCACTGCAACTTCCCCCTCGCGGGTTCGAGCGATTCTCCTGCCCCAGCCTCCTGAGTAGC A G RNF10 Ensembl:ENSG00000022840 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs901109785 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88407,RMVar_hsa_circ_86391,RMVar_hsa_circ_160802,RMVar_hsa_circ_160803,RMVar_hsa_circ_307791,RMVar_hsa_circ_27491,RMVar_hsa_circ_160816,RMVar_hsa_circ_327844,RMVar_hsa_circ_160810,RMVar_hsa_circ_375920,RMVar_hsa_circ_160815,RMVar_hsa_circ_37149,RMVar_hsa_circ_83786,RMVar_hsa_circ_160817,RMVar_hsa_circ_84745,RMVar_hsa_circ_88087,RMVar_hsa_circ_16332,RMVar_hsa_circ_160825,RMVar_hsa_circ_160828,RMVar_hsa_circ_309102,RMVar_hsa_circ_160826,RMVar_hsa_circ_376353,RMVar_hsa_circ_160829,RMVar_hsa_circ_122660,RMVar_hsa_circ_286489,RMVar_hsa_circ_106013,RMVar_hsa_circ_160830,RMVar_hsa_circ_160831,RMVar_hsa_circ_160832 35187 RMVar_ID_35187 Human_SNP_ID_518156919 A-to-I Human chr12 + 120570223 120570223 120570223 TTTTTTTTTTTTTTAAGATGGAGTTTTGCTCTATCACCCAGGCTGGAGCACAATGGCACGATCTC TTTTTTTTTTTTTTAAGATGGAGTTTTGCTCTCTCACCCAGGCTGGAGCACAATGGCACGATCTC A C RNF10 Ensembl:ENSG00000022840 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs996723917 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88407,RMVar_hsa_circ_86391,RMVar_hsa_circ_160802,RMVar_hsa_circ_160803,RMVar_hsa_circ_307791,RMVar_hsa_circ_27491,RMVar_hsa_circ_160816,RMVar_hsa_circ_327844,RMVar_hsa_circ_160810,RMVar_hsa_circ_375920,RMVar_hsa_circ_160815,RMVar_hsa_circ_37149,RMVar_hsa_circ_83786,RMVar_hsa_circ_160817,RMVar_hsa_circ_84745,RMVar_hsa_circ_88087,RMVar_hsa_circ_16332,RMVar_hsa_circ_160825,RMVar_hsa_circ_160828,RMVar_hsa_circ_309102,RMVar_hsa_circ_160826,RMVar_hsa_circ_376353,RMVar_hsa_circ_160829,RMVar_hsa_circ_122660,RMVar_hsa_circ_286489,RMVar_hsa_circ_106013,RMVar_hsa_circ_160830,RMVar_hsa_circ_160831,RMVar_hsa_circ_160832 35188 RMVar_ID_35188 Human_SNP_ID_518156920 A-to-I Human chr12 + 120570223 120570223 120570223 TTTTTTTTTTTTTTAAGATGGAGTTTTGCTCTATCACCCAGGCTGGAGCACAATGGCACGATCTC TTTTTTTTTTTTTTAAGATGGAGTTTTGCTCTGTCACCCAGGCTGGAGCACAATGGCACGATCTC A G RNF10 Ensembl:ENSG00000022840 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs996723917 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88407,RMVar_hsa_circ_86391,RMVar_hsa_circ_160802,RMVar_hsa_circ_160803,RMVar_hsa_circ_307791,RMVar_hsa_circ_27491,RMVar_hsa_circ_160816,RMVar_hsa_circ_327844,RMVar_hsa_circ_160810,RMVar_hsa_circ_375920,RMVar_hsa_circ_160815,RMVar_hsa_circ_37149,RMVar_hsa_circ_83786,RMVar_hsa_circ_160817,RMVar_hsa_circ_84745,RMVar_hsa_circ_88087,RMVar_hsa_circ_16332,RMVar_hsa_circ_160825,RMVar_hsa_circ_160828,RMVar_hsa_circ_309102,RMVar_hsa_circ_160826,RMVar_hsa_circ_376353,RMVar_hsa_circ_160829,RMVar_hsa_circ_122660,RMVar_hsa_circ_286489,RMVar_hsa_circ_106013,RMVar_hsa_circ_160830,RMVar_hsa_circ_160831,RMVar_hsa_circ_160832 35189 RMVar_ID_35189 Human_SNP_ID_518163101 A-to-I Human chr12 - 120594058 120594058 120594058 CAAACACAGAATCAGCAAAGAGGAGACCATGCACTGGCTCCAACAGAAGTGTGATGGGATCATGC CAAACACAGAATCAGCAAAGAGGAGACCATGCGCTGGCTCCAACAGAAGTGTGATGGGATCATGC T C RPL11P5 Ensembl:ENSG00000242137 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1480730748 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1829291,Human_miRNA_ID_1829504,Human_miRNA_ID_1830135 35190 RMVar_ID_35190 Human_SNP_ID_518172908 A-to-I Human chr12 - 120634530 120634522 120634530 AGAGGATGTCAAGATTTTTATTTTTCAAGACAAAGTCTCACTCAGTTGCCCAGGCTGGAGTTCAG AGAGGATGTCAAGATTTTTATTTTTCAAGACA________CTCAGTTGCCCAGGCTGGAGTTCAG GTGAGACTT G AC125616.1 Ensembl:ENSG00000256008 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1436360564 Functional Loss DEL dbSNP153 33..40 33 - - - 35191 RMVar_ID_35191 Human_SNP_ID_518175563 A-to-I Human chr12 + 120645014 120645014 120645014 GTTAGTAGAGATGGAGTTTCACCACGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAAGTGATC GTTAGTAGAGATGGAGTTTCACCACGTTGGCCGGGCTGGTCTCGAACTCCTGACCTCAAGTGATC A G CABP1 Ensembl:ENSG00000157782 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1322296700 Functional Loss SNV dbSNP153 33..33 33 - - - 35192 RMVar_ID_35192 Human_SNP_ID_518175742 A-to-I Human chr12 + 120645952 120645952 120645952 TCACATCTGTAATTGCAGCACTTTGGGAGGCCAAGTCAGGAGGATTGCTTGAGCCCAAGAGTTTG TCACATCTGTAATTGCAGCACTTTGGGAGGCCGAGTCAGGAGGATTGCTTGAGCCCAAGAGTTTG A G CABP1 Ensembl:ENSG00000157782 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs945614900 Functional Loss SNV dbSNP153 33..33 33 - - - 35193 RMVar_ID_35193 Human_SNP_ID_518177434 A-to-I Human chr12 + 120653093 120653093 120653093 ATGCAGTGGAAATTCCCCAGCTACCACTCTCCATTCTTCATGGGAGCAAATTCCTCTCCATCCTT ATGCAGTGGAAATTCCCCAGCTACCACTCTCCGTTCTTCATGGGAGCAAATTCCTCTCCATCCTT A G CABP1 Ensembl:ENSG00000157782 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1456002972 Functional Loss SNV dbSNP153 33..33 33 - - - 35194 RMVar_ID_35194 Human_SNP_ID_518177946 A-to-I Human chr12 + 120655257 120655257 120655257 CGAGACCACCCTGGCCAACATGGTGAAACCCCATCTCTGCTGAAAATACGGAAAAAAAAATTAGC CGAGACCACCCTGGCCAACATGGTGAAACCCCTTCTCTGCTGAAAATACGGAAAAAAAAATTAGC A T CABP1 Ensembl:ENSG00000157782 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1405585223 Functional Loss SNV dbSNP153 33..33 33 - - - 35195 RMVar_ID_35195 Human_SNP_ID_518178455 A-to-I Human chr12 + 120656836 120656836 120656836 AGAATCGCTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCCAAGGTCGCGCCATGGCACTCCAGCC AGAATCGCTTGAACCCAGGAGGCAGAGGTTGCGGTGAGCCAAGGTCGCGCCATGGCACTCCAGCC A G CABP1 Ensembl:ENSG00000157782 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs770188249 Functional Loss SNV dbSNP153 33..33 33 - - - 35196 RMVar_ID_35196 Human_SNP_ID_518178583 A-to-I Human chr12 + 120657480 120657480 120657480 TGCCTGAGGAAGTAGATCTGAGCTTCATACTCAGGTCTGTCTGCCTCTAGAGTCCAAGTGCGTCT TGCCTGAGGAAGTAGATCTGAGCTTCATACTCGGGTCTGTCTGCCTCTAGAGTCCAAGTGCGTCT A G CABP1 Ensembl:ENSG00000157782 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1454056405 Functional Loss SNV dbSNP153 33..33 33 - - - 35197 RMVar_ID_35197 Human_SNP_ID_518189552 A-to-I Human chr12 + 120701721 120701721 120701721 CCTGGTTGGCCGGGGAAGCTGTAGGGGTGGATAGAGCTGGCTTTCCTTCTGGGCTGTCTCCATCT CCTGGTTGGCCGGGGAAGCTGTAGGGGTGGATGGAGCTGGCTTTCCTTCTGGGCTGTCTCCATCT A G MLEC Ensembl:ENSG00000110917 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs574808706 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_228631,Human_RBP_ID_412762,Human_RBP_ID_753215,Human_RBP_ID_6143051,Human_RBP_ID_8367478,Human_RBP_ID_8777109,Human_RBP_ID_11845038,Human_RBP_ID_18256237,Human_RBP_ID_23542482 Human_miRNA_ID_1970969 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 35198 RMVar_ID_35198 Human_SNP_ID_518192842 A-to-I Human chr12 + 120715018 120715018 120715018 TGAGACCAGCCTGGGCAACATGGCAAAACCCCATCTGTACAAAAAATACAAAAAAATTAGCCAGG TGAGACCAGCCTGGGCAACATGGCAAAACCCCGTCTGTACAAAAAATACAAAAAAATTAGCCAGG A G UNC119B Ensembl:ENSG00000175970 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs965462460 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117258,RMVar_hsa_circ_160843 35199 RMVar_ID_35199 Human_SNP_ID_518206329 A-to-I Human chr12 - 120762971 120762971 120762971 CCTTCCTTCCTTCTCAGCCCTCGAGGATGCATATAGCTAATTAAGCAGGCCCAGAGACAGAGAGG CCTTCCTTCCTTCTCAGCCCTCGAGGATGCATGTAGCTAATTAAGCAGGCCCAGAGACAGAGAGG T C SPPL3 Ensembl:ENSG00000157837 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs544024979 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265015 35200 RMVar_ID_35200 Human_SNP_ID_518206330 A-to-I Human chr12 - 120762971 120762971 120762971 CCTTCCTTCCTTCTCAGCCCTCGAGGATGCATATAGCTAATTAAGCAGGCCCAGAGACAGAGAGG CCTTCCTTCCTTCTCAGCCCTCGAGGATGCATCTAGCTAATTAAGCAGGCCCAGAGACAGAGAGG T G SPPL3 Ensembl:ENSG00000157837 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs544024979 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265015 35201 RMVar_ID_35201 Human_SNP_ID_518210869 A-to-I Human chr12 - 120780147 120780147 120780147 GGATGGGAGGATTGCTTGAGGCGAGGAGTTCAAGACCAGCCTGGGCAACATAGTGAGACTGCATC GGATGGGAGGATTGCTTGAGGCGAGGAGTTCAGGACCAGCCTGGGCAACATAGTGAGACTGCATC T C SPPL3 Ensembl:ENSG00000157837 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1473783812 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 35202 RMVar_ID_35202 Human_SNP_ID_518210945 A-to-I Human chr12 - 120780442 120780442 120780442 CTCCCCCAGCTTTTTTTGTTTTGTTTGGAGACAGGGCCTTACTCTGTTGCTCAGGCTGGAGTGCA CTCCCCCAGCTTTTTTTGTTTTGTTTGGAGACGGGGCCTTACTCTGTTGCTCAGGCTGGAGTGCA T C SPPL3 Ensembl:ENSG00000157837 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs899845057 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11845698,Human_RBP_ID_21885613 RMVar_hsa_circ_271105,RMVar_hsa_circ_265688,RMVar_hsa_circ_68822,RMVar_hsa_circ_160855,RMVar_hsa_circ_342598,RMVar_hsa_circ_266422 35203 RMVar_ID_35203 Human_SNP_ID_518223357 A-to-I Human chr12 - 120828962 120828962 120828962 GCCCAGGAGCTCATGACCAGCCTGGGCAACATAGAGAGACCCCCATCTCTACAAGAAATAAAAAT GCCCAGGAGCTCATGACCAGCCTGGGCAACATTGAGAGACCCCCATCTCTACAAGAAATAAAAAT T A SPPL3 Ensembl:ENSG00000157837 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1410314915 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101372,RMVar_hsa_circ_160862 35204 RMVar_ID_35204 Human_SNP_ID_518229040 A-to-I Human chr12 - 120850476 120850476 120850476 TTTTTTTTTTTTTTTTAAAGGCTGGTCTCACTATGTTGTCCAGGCTGGTCTTGAACTCTTGGGCT TTTTTTTTTTTTTTTTAAAGGCTGGTCTCACTTTGTTGTCCAGGCTGGTCTTGAACTCTTGGGCT T A SPPL3 Ensembl:ENSG00000157837 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs958034891 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101372,RMVar_hsa_circ_160862 35205 RMVar_ID_35205 Human_SNP_ID_518230144 A-to-I Human chr12 - 120853524 120853524 120853524 CATATCTTCTTCTTAGTCTAAAATTTATATCAAAAGAATTAGGAATACTATGGTTTGTTACAGCT CATATCTTCTTCTTAGTCTAAAATTTATATCAGAAGAATTAGGAATACTATGGTTTGTTACAGCT T C SPPL3 Ensembl:ENSG00000157837 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs74843871 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8367547 RMVar_hsa_circ_101372,RMVar_hsa_circ_160862 35206 RMVar_ID_35206 Human_SNP_ID_518232735 A-to-I Human chr12 - 120863720 120863720 120863720 GGAGGATAGCTTCAGCCCAGGAGTTCGAGGCTACAGTCAGCTGTGATCACTCCAGCCTGAGCAAT GGAGGATAGCTTCAGCCCAGGAGTTCGAGGCTGCAGTCAGCTGTGATCACTCCAGCCTGAGCAAT T C SPPL3 Ensembl:ENSG00000157837 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1204616596 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101372,RMVar_hsa_circ_160862 35207 RMVar_ID_35207 Human_SNP_ID_518232740 A-to-I Human chr12 - 120863734 120863734 120863734 GGGAGGTTGAGGCAGGAGGATAGCTTCAGCCCAGGAGTTCGAGGCTACAGTCAGCTGTGATCACT GGGAGGTTGAGGCAGGAGGATAGCTTCAGCCCGGGAGTTCGAGGCTACAGTCAGCTGTGATCACT T C SPPL3 Ensembl:ENSG00000157837 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1180084664 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101372,RMVar_hsa_circ_160862 35208 RMVar_ID_35208 Human_SNP_ID_518232920 A-to-I Human chr12 - 120864452 120864452 120864452 CGGCTCGCTGCAGCCTCCGACTCCCAGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCCAAGTAGCT CGGCTCGCTGCAGCCTCCGACTCCCAGGTTCAGGCAGTTCTCCTGCCTCAGCCTCCCAAGTAGCT T C SPPL3 Ensembl:ENSG00000157837 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs997610345 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101372,RMVar_hsa_circ_160862 35209 RMVar_ID_35209 Human_SNP_ID_518233674 A-to-I Human chr12 - 120867543 120867543 120867543 CCTCTGCCTCAGCCTCTCAAGTAGCTGGGACTACAGGCACGTACCATCACACCCAGCTAGTTTTT CCTCTGCCTCAGCCTCTCAAGTAGCTGGGACTGCAGGCACGTACCATCACACCCAGCTAGTTTTT T C SPPL3 Ensembl:ENSG00000157837 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs769417133 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101372,RMVar_hsa_circ_160862 35210 RMVar_ID_35210 Human_SNP_ID_518233687 A-to-I Human chr12 - 120867582 120867582 120867582 TGGCTCCCTGCAACCTCCGCCTCCCGGGTTCAAGCGATTCCTCTGCCTCAGCCTCTCAAGTAGCT TGGCTCCCTGCAACCTCCGCCTCCCGGGTTCAGGCGATTCCTCTGCCTCAGCCTCTCAAGTAGCT T C SPPL3 Ensembl:ENSG00000157837 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs962213616 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101372,RMVar_hsa_circ_160862 35211 RMVar_ID_35211 Human_SNP_ID_518234276 A-to-I Human chr12 - 120869666 120869666 120869666 TAGCGAAAATGCTAACATAAGAAGTAAATAGTAGCAAGCAAAGGATTTTTAAAATATCCAACCTA TAGCGAAAATGCTAACATAAGAAGTAAATAGTGGCAAGCAAAGGATTTTTAAAATATCCAACCTA T C SPPL3 Ensembl:ENSG00000157837 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs916908917 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101372,RMVar_hsa_circ_160862 35212 RMVar_ID_35212 Human_SNP_ID_518237913 A-to-I Human chr12 - 120882817 120882817 120882817 GCCATCATAGTTAACTGTAACCTTGAACTCCTAGCCTCAAGCAATCTTTCGCCTTGGCTTCCCAC GCCATCATAGTTAACTGTAACCTTGAACTCCTGGCCTCAAGCAATCTTTCGCCTTGGCTTCCCAC T C SPPL3 Ensembl:ENSG00000157837 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs578230401 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101372,RMVar_hsa_circ_160862 35213 RMVar_ID_35213 Human_SNP_ID_518239320 A-to-I Human chr12 - 120888187 120888187 120888187 CCTGTAATCCCAGCTACTCAGGAGGCTGAGGTAGGAGAATCACTTGAACGCAAGAGGCAGAGGTT CCTGTAATCCCAGCTACTCAGGAGGCTGAGGTGGGAGAATCACTTGAACGCAAGAGGCAGAGGTT T C SPPL3 Ensembl:ENSG00000157837 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1377661224 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101372,RMVar_hsa_circ_160862 35214 RMVar_ID_35214 Human_SNP_ID_518242067 A-to-I Human chr12 - 120898127 120898127 120898127 GCTAATTTTTTGTAGACATGAGGTTTTGCCATATTGGCCAGGTTGGTCTCGAACTCCTGACTTCA GCTAATTTTTTGTAGACATGAGGTTTTGCCATGTTGGCCAGGTTGGTCTCGAACTCCTGACTTCA T C SPPL3 Ensembl:ENSG00000157837 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335860561 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11847357 RMVar_hsa_circ_101372,RMVar_hsa_circ_160862 35215 RMVar_ID_35215 Human_SNP_ID_518324470 A-to-I Human chr12 + 121212316 121212316 121212316 GCCCACACCCAGATTTGGACTCATTGGCTCACACCTGTAGTCCCAGTGCTTTGGGAAGCCAAGGT GCCCACACCCAGATTTGGACTCATTGGCTCACTCCTGTAGTCCCAGTGCTTTGGGAAGCCAAGGT A T P2RX4 Ensembl:ENSG00000135124 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1023383417 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80220,RMVar_hsa_circ_108760,RMVar_hsa_circ_160870,RMVar_hsa_circ_160871 35216 RMVar_ID_35216 Human_SNP_ID_518324813 A-to-I Human chr12 + 121213155 121213155 121213155 AAAGACATAGTACAGAAAAAGAGGCTGGGCACAGTGGCTCATGCCTGAAATCACAGTACTTTGGG AAAGACATAGTACAGAAAAAGAGGCTGGGCACCGTGGCTCATGCCTGAAATCACAGTACTTTGGG A C P2RX4 Ensembl:ENSG00000135124 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs910735129 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80220,RMVar_hsa_circ_108760,RMVar_hsa_circ_160870,RMVar_hsa_circ_160871 35217 RMVar_ID_35217 Human_SNP_ID_518324942 A-to-I Human chr12 + 121213770 121213770 121213770 ATCTCTACAATCATGAGGTTTCCATGTTGCCCAGGCTGGTCTCGAACTCCTGAGCTCTAGCAATC ATCTCTACAATCATGAGGTTTCCATGTTGCCCCGGCTGGTCTCGAACTCCTGAGCTCTAGCAATC A C P2RX4 Ensembl:ENSG00000135124 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs964215324 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80220,RMVar_hsa_circ_108760,RMVar_hsa_circ_160870,RMVar_hsa_circ_160871 35218 RMVar_ID_35218 Human_SNP_ID_518324980 A-to-I Human chr12 + 121213971 121213971 121213971 CCTGTAATCCCAATACTTTGGGAGGCTGAGGCAAGTGGATCCCTTGAGCTTAGGAATTTTGAGAC CCTGTAATCCCAATACTTTGGGAGGCTGAGGCCAGTGGATCCCTTGAGCTTAGGAATTTTGAGAC A C P2RX4 Ensembl:ENSG00000135124 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1445360522 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80220,RMVar_hsa_circ_108760,RMVar_hsa_circ_160870,RMVar_hsa_circ_160871 35219 RMVar_ID_35219 Human_SNP_ID_518324991 A-to-I Human chr12 + 121214055 121214055 121214055 AAACCCCATCTCTACCAAAAATACGAAAAATTAGCTTGGCATAGTGGCGCACACCTGTGGACCCA AAACCCCATCTCTACCAAAAATACGAAAAATTGGCTTGGCATAGTGGCGCACACCTGTGGACCCA A G P2RX4 Ensembl:ENSG00000135124 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1481091176 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80220,RMVar_hsa_circ_108760,RMVar_hsa_circ_160870,RMVar_hsa_circ_160871 35220 RMVar_ID_35220 Human_SNP_ID_518325213 A-to-I Human chr12 + 121214969 121214969 121214969 ACCACACCCAGCTAATTTTGTGTATTTTTAGTAGAGTCGGGGTTTCACAATGTTGGCCAGGCTGG ACCACACCCAGCTAATTTTGTGTATTTTTAGTCGAGTCGGGGTTTCACAATGTTGGCCAGGCTGG A C P2RX4 Ensembl:ENSG00000135124 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs112485293 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80220,RMVar_hsa_circ_108760,RMVar_hsa_circ_160870,RMVar_hsa_circ_160871 35221 RMVar_ID_35221 Human_SNP_ID_518325214 A-to-I Human chr12 + 121214969 121214969 121214969 ACCACACCCAGCTAATTTTGTGTATTTTTAGTAGAGTCGGGGTTTCACAATGTTGGCCAGGCTGG ACCACACCCAGCTAATTTTGTGTATTTTTAGTTGAGTCGGGGTTTCACAATGTTGGCCAGGCTGG A T P2RX4 Ensembl:ENSG00000135124 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs112485293 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80220,RMVar_hsa_circ_108760,RMVar_hsa_circ_160870,RMVar_hsa_circ_160871 35222 RMVar_ID_35222 Human_SNP_ID_518325219 A-to-I Human chr12 + 121214985 121214985 121214985 TTTGTGTATTTTTAGTAGAGTCGGGGTTTCACAATGTTGGCCAGGCTGGTCTTGGACTCCTGACC TTTGTGTATTTTTAGTAGAGTCGGGGTTTCACTATGTTGGCCAGGCTGGTCTTGGACTCCTGACC A T P2RX4 Ensembl:ENSG00000135124 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1054805002 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80220,RMVar_hsa_circ_108760,RMVar_hsa_circ_160870,RMVar_hsa_circ_160871 35223 RMVar_ID_35223 Human_SNP_ID_518328313 A-to-I Human chr12 + 121226038 121226038 121226038 AGCTGGGACCACAGGGGCGCACCACCATGCCCAGCCAACTTATTTTTTGTAGAGACAGGGTCTCA AGCTGGGACCACAGGGGCGCACCACCATGCCCGGCCAACTTATTTTTTGTAGAGACAGGGTCTCA A G P2RX4 Ensembl:ENSG00000135124 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1464459126 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61092,RMVar_hsa_circ_108760,RMVar_hsa_circ_160871,RMVar_hsa_circ_367007,RMVar_hsa_circ_55701 35224 RMVar_ID_35224 Human_SNP_ID_518328786 A-to-I Human chr12 + 121227974 121227974 121227974 TTCATTAGCCAGGCATGGTGATGCATGCCTATAGTTCCAGCTACTTGAGAGGCTGAGGTGGGAGA TTCATTAGCCAGGCATGGTGATGCATGCCTATGGTTCCAGCTACTTGAGAGGCTGAGGTGGGAGA A G P2RX4 Ensembl:ENSG00000135124 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs112593845 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61092,RMVar_hsa_circ_108760,RMVar_hsa_circ_160871,RMVar_hsa_circ_367007,RMVar_hsa_circ_55701 35225 RMVar_ID_35225 Human_SNP_ID_518328787 A-to-I Human chr12 + 121227974 121227974 121227974 TTCATTAGCCAGGCATGGTGATGCATGCCTATAGTTCCAGCTACTTGAGAGGCTGAGGTGGGAGA TTCATTAGCCAGGCATGGTGATGCATGCCTATTGTTCCAGCTACTTGAGAGGCTGAGGTGGGAGA A T P2RX4 Ensembl:ENSG00000135124 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs112593845 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61092,RMVar_hsa_circ_108760,RMVar_hsa_circ_160871,RMVar_hsa_circ_367007,RMVar_hsa_circ_55701 35226 RMVar_ID_35226 Human_SNP_ID_518331052 A-to-I Human chr12 + 121235659 121235659 121235659 TACAAAAAATTAAATTAGCCGGGTGTGGCGGTATATATCTGTAGTCCCAGCTACTTGGGTGGCTG TACAAAAAATTAAATTAGCCGGGTGTGGCGGTGTATATCTGTAGTCCCAGCTACTTGGGTGGCTG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1174862954 Functional Loss SNV dbSNP153 33..33 33 - - - 35227 RMVar_ID_35227 Human_SNP_ID_518331054 A-to-I Human chr12 + 121235661 121235661 121235661 CAAAAAATTAAATTAGCCGGGTGTGGCGGTATATATCTGTAGTCCCAGCTACTTGGGTGGCTGAG CAAAAAATTAAATTAGCCGGGTGTGGCGGTATGTATCTGTAGTCCCAGCTACTTGGGTGGCTGAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs892166332 Functional Loss SNV dbSNP153 33..33 33 - - - 35228 RMVar_ID_35228 Human_SNP_ID_518333127 A-to-I Human chr12 - 121243884 121243884 121243884 GGGACCCCACTGCCCTTCCCACTGAGCACATCATGGCTACCTGACTTGGTGGGAGCTCCAGGCAG GGGACCCCACTGCCCTTCCCACTGAGCACATCGTGGCTACCTGACTTGGTGGGAGCTCCAGGCAG T C CAMKK2 Ensembl:ENSG00000110931 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1063843 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_3924,GWAS_ID_3925,GWAS_ID_3926,GWAS_ID_3927,GWAS_ID_3928,GWAS_ID_3929,GWAS_ID_3930,GWAS_ID_3931,GWAS_ID_3932,GWAS_ID_3933,GWAS_ID_3934,GWAS_ID_3935,GWAS_ID_3936,GWAS_ID_3937,GWAS_ID_3938,GWAS_ID_3939,GWAS_ID_3940,GWAS_ID_3941,GWAS_ID_3942,GWAS_ID_3943,GWAS_ID_3944,GWAS_ID_3945 RMVar_hsa_circ_119675,RMVar_hsa_circ_160875 35229 RMVar_ID_35229 Human_SNP_ID_518338143 A-to-I Human chr12 - 121262323 121262323 121262323 TATTTTTAATGGAGATGGGGTTTCACCGTGTTAGTCAGGATGGTCTTGATCTCCTGAACTCGTGA TATTTTTAATGGAGATGGGGTTTCACCGTGTTGGTCAGGATGGTCTTGATCTCCTGAACTCGTGA T C CAMKK2 Ensembl:ENSG00000110931 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs565478945 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_160880,RMVar_hsa_circ_119675,RMVar_hsa_circ_160875,RMVar_hsa_circ_73520,RMVar_hsa_circ_115621,RMVar_hsa_circ_371958,RMVar_hsa_circ_374227,RMVar_hsa_circ_123455,RMVar_hsa_circ_87700,RMVar_hsa_circ_78673,RMVar_hsa_circ_160882,RMVar_hsa_circ_160883,RMVar_hsa_circ_160881,RMVar_hsa_circ_160878,RMVar_hsa_circ_160879,RMVar_hsa_circ_277182,RMVar_hsa_circ_160890 35230 RMVar_ID_35230 Human_SNP_ID_518338389 A-to-I Human chr12 - 121263359 121263359 121263359 CGCGCTTATAATGACAGCACTCTGGGAGGCCAAGGTGGACAGATCACTTGAGATCAGGAGTTTGA CGCGCTTATAATGACAGCACTCTGGGAGGCCACGGTGGACAGATCACTTGAGATCAGGAGTTTGA T G CAMKK2 Ensembl:ENSG00000110931 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1011050257 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_160880,RMVar_hsa_circ_119675,RMVar_hsa_circ_160875,RMVar_hsa_circ_73520,RMVar_hsa_circ_115621,RMVar_hsa_circ_371958,RMVar_hsa_circ_374227,RMVar_hsa_circ_123455,RMVar_hsa_circ_87700,RMVar_hsa_circ_78673,RMVar_hsa_circ_160882,RMVar_hsa_circ_160883,RMVar_hsa_circ_160881,RMVar_hsa_circ_160878,RMVar_hsa_circ_160879,RMVar_hsa_circ_277182,RMVar_hsa_circ_160890 35231 RMVar_ID_35231 Human_SNP_ID_518339065 A-to-I Human chr12 - 121266070 121266070 121266070 AAAATTAGCTGGGCATGGTGGTGTGCACCTGTAGTCCTAGCTACTCGGGAGGCTGAGGCGGGAGG AAAATTAGCTGGGCATGGTGGTGTGCACCTGTCGTCCTAGCTACTCGGGAGGCTGAGGCGGGAGG T G CAMKK2 Ensembl:ENSG00000110931 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1037016858 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_160880,RMVar_hsa_circ_73520,RMVar_hsa_circ_115621,RMVar_hsa_circ_371958,RMVar_hsa_circ_374227,RMVar_hsa_circ_87700,RMVar_hsa_circ_78673,RMVar_hsa_circ_160882,RMVar_hsa_circ_160881,RMVar_hsa_circ_27605,RMVar_hsa_circ_160878,RMVar_hsa_circ_160879,RMVar_hsa_circ_325323,RMVar_hsa_circ_334518,RMVar_hsa_circ_282648 35232 RMVar_ID_35232 Human_SNP_ID_518344003 A-to-I Human chr12 - 121285806 121285806 121285806 TTGGGTCACACATCTACTCTCTTTTTTGAGACAGGGTCTCGCTCTGTCACCCAGGCTAGAGTGCG TTGGGTCACACATCTACTCTCTTTTTTGAGACGGGGTCTCGCTCTGTCACCCAGGCTAGAGTGCG T C CAMKK2 Ensembl:ENSG00000110931 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1248907308 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115621,RMVar_hsa_circ_160878 35233 RMVar_ID_35233 Human_SNP_ID_518345583 A-to-I Human chr12 - 121292402 121292402 121292402 GAGGAGGGCTGGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGTAG GAGGAGGGCTGGGCACGGTGGCTCACGCCTGTCATCCCAGCACTTTGGGAGGCCGAGGCGGGTAG T G CAMKK2 Ensembl:ENSG00000110931 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459985925 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115621,RMVar_hsa_circ_160878 35234 RMVar_ID_35234 Human_SNP_ID_518353676 A-to-I Human chr12 - 121324968 121324968 121324968 TAGAGATGGAATCTCACTCTGTTGCCCAGGCTAGTCTCAAATTTCTGGGCTCAAGCAGTCCTCCC TAGAGATGGAATCTCACTCTGTTGCCCAGGCTCGTCTCAAATTTCTGGGCTCAAGCAGTCCTCCC T G ANAPC5 Ensembl:ENSG00000089053 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1315711157 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9667551,Human_RBP_ID_11848717 RMVar_hsa_circ_16571,RMVar_hsa_circ_95026,RMVar_hsa_circ_111714,RMVar_hsa_circ_13766,RMVar_hsa_circ_160896,RMVar_hsa_circ_370329,RMVar_hsa_circ_373039,RMVar_hsa_circ_160902,RMVar_hsa_circ_160903,RMVar_hsa_circ_160901,RMVar_hsa_circ_27800,RMVar_hsa_circ_160904,RMVar_hsa_circ_101348 35235 RMVar_ID_35235 Human_SNP_ID_518355211 A-to-I Human chr12 - 121331888 121331888 121331888 GCAGTGAGCTAGGATTGTGCCACTGTACTCCAACCTGGGTGACAGAGGGAGACCCTGTCTCTAAA GCAGTGAGCTAGGATTGTGCCACTGTACTCCAGCCTGGGTGACAGAGGGAGACCCTGTCTCTAAA T C ANAPC5 Ensembl:ENSG00000089053 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1555272960 Functional Loss SNV dbSNP153 33..33 33 - - - 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_160906,RMVar_hsa_circ_45517,RMVar_hsa_circ_313313,RMVar_hsa_circ_371671,RMVar_hsa_circ_358407,RMVar_hsa_circ_375911,RMVar_hsa_circ_76171,RMVar_hsa_circ_160907,RMVar_hsa_circ_36437,RMVar_hsa_circ_160905 35236 RMVar_ID_35236 Human_SNP_ID_518355240 A-to-I Human chr12 - 121332026 121332026 121332026 GTTTACCAGCCTGGGGAACATAGTGAGACTCTATATCTATTTTTAAAAAAATTAGCCGACCAAGC GTTTACCAGCCTGGGGAACATAGTGAGACTCTGTATCTATTTTTAAAAAAATTAGCCGACCAAGC T C ANAPC5 Ensembl:ENSG00000089053 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1555272975 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11849008,Human_RBP_ID_27623867 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_160906,RMVar_hsa_circ_45517,RMVar_hsa_circ_313313,RMVar_hsa_circ_371671,RMVar_hsa_circ_358407,RMVar_hsa_circ_375911,RMVar_hsa_circ_76171,RMVar_hsa_circ_160907,RMVar_hsa_circ_36437,RMVar_hsa_circ_160905 35237 RMVar_ID_35237 Human_SNP_ID_518355286 A-to-I Human chr12 - 121332238 121332238 121332238 TAGCTTTGGGCTGGGCACCATAGCTCATGCCTATAATCCCAGCACTTTGGGAGGCCAAAGAAGGA TAGCTTTGGGCTGGGCACCATAGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAAGAAGGA T C ANAPC5 Ensembl:ENSG00000089053 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs1439149834 Functional Loss SNV dbSNP153 33..33 33 - - - 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_160906,RMVar_hsa_circ_45517,RMVar_hsa_circ_313313,RMVar_hsa_circ_371671,RMVar_hsa_circ_358407,RMVar_hsa_circ_375911,RMVar_hsa_circ_76171,RMVar_hsa_circ_160907,RMVar_hsa_circ_36437,RMVar_hsa_circ_160905 35238 RMVar_ID_35238 Human_SNP_ID_518355420 A-to-I Human chr12 - 121332882 121332882 121332882 TGGCCTCCCAAAGTGCTGGGATTATAGGCATAAGCTACTGCACCCATCTCAGAATTTGTCTATGT TGGCCTCCCAAAGTGCTGGGATTATAGGCATACGCTACTGCACCCATCTCAGAATTTGTCTATGT T G ANAPC5 Ensembl:ENSG00000089053 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1555273054 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6144057 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_160906,RMVar_hsa_circ_45517,RMVar_hsa_circ_313313,RMVar_hsa_circ_371671,RMVar_hsa_circ_358407,RMVar_hsa_circ_375911,RMVar_hsa_circ_76171,RMVar_hsa_circ_160907,RMVar_hsa_circ_36437,RMVar_hsa_circ_160905 35239 RMVar_ID_35239 Human_SNP_ID_518355421 A-to-I Human chr12 - 121332883 121332883 121332883 TTGGCCTCCCAAAGTGCTGGGATTATAGGCATAAGCTACTGCACCCATCTCAGAATTTGTCTATG TTGGCCTCCCAAAGTGCTGGGATTATAGGCATGAGCTACTGCACCCATCTCAGAATTTGTCTATG T C ANAPC5 Ensembl:ENSG00000089053 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1029653514 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6144057 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_160906,RMVar_hsa_circ_45517,RMVar_hsa_circ_313313,RMVar_hsa_circ_371671,RMVar_hsa_circ_358407,RMVar_hsa_circ_375911,RMVar_hsa_circ_76171,RMVar_hsa_circ_160907,RMVar_hsa_circ_36437,RMVar_hsa_circ_160905 35240 RMVar_ID_35240 Human_SNP_ID_518355423 A-to-I Human chr12 - 121332889 121332889 121332889 CCCACCTTGGCCTCCCAAAGTGCTGGGATTATAGGCATAAGCTACTGCACCCATCTCAGAATTTG CCCACCTTGGCCTCCCAAAGTGCTGGGATTATGGGCATAAGCTACTGCACCCATCTCAGAATTTG T C ANAPC5 Ensembl:ENSG00000089053 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1379612969 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6144057 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_160906,RMVar_hsa_circ_45517,RMVar_hsa_circ_313313,RMVar_hsa_circ_371671,RMVar_hsa_circ_358407,RMVar_hsa_circ_375911,RMVar_hsa_circ_76171,RMVar_hsa_circ_160907,RMVar_hsa_circ_36437,RMVar_hsa_circ_160905 35241 RMVar_ID_35241 Human_SNP_ID_518355431 A-to-I Human chr12 - 121332918 121332918 121332918 TTCTTGAACGCCTGGTCTCAAGTGATCCTCCCACCTTGGCCTCCCAAAGTGCTGGGATTATAGGC TTCTTGAACGCCTGGTCTCAAGTGATCCTCCCGCCTTGGCCTCCCAAAGTGCTGGGATTATAGGC T C ANAPC5 Ensembl:ENSG00000089053 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs560221009 Functional Loss SNV dbSNP153 33..33 33 - - - 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_160906,RMVar_hsa_circ_45517,RMVar_hsa_circ_313313,RMVar_hsa_circ_371671,RMVar_hsa_circ_358407,RMVar_hsa_circ_375911,RMVar_hsa_circ_76171,RMVar_hsa_circ_160907,RMVar_hsa_circ_36437,RMVar_hsa_circ_160905 35242 RMVar_ID_35242 Human_SNP_ID_518355437 A-to-I Human chr12 - 121332931 121332931 121332931 GTTGCCCAGGTTGTTCTTGAACGCCTGGTCTCAAGTGATCCTCCCACCTTGGCCTCCCAAAGTGC GTTGCCCAGGTTGTTCTTGAACGCCTGGTCTCGAGTGATCCTCCCACCTTGGCCTCCCAAAGTGC T C ANAPC5 Ensembl:ENSG00000089053 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1135183 Functional Loss SNV dbSNP153 33..33 33 - - - 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_160906,RMVar_hsa_circ_45517,RMVar_hsa_circ_313313,RMVar_hsa_circ_371671,RMVar_hsa_circ_358407,RMVar_hsa_circ_375911,RMVar_hsa_circ_76171,RMVar_hsa_circ_160907,RMVar_hsa_circ_36437,RMVar_hsa_circ_160905 35243 RMVar_ID_35243 Human_SNP_ID_518355449 A-to-I Human chr12 - 121332965 121332965 121332965 TATTTTTAAAAATATAGAGACAAGGTTTTGCTATGTTGCCCAGGTTGTTCTTGAACGCCTGGTCT TATTTTTAAAAATATAGAGACAAGGTTTTGCTGTGTTGCCCAGGTTGTTCTTGAACGCCTGGTCT T C ANAPC5 Ensembl:ENSG00000089053 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1135182 Functional Loss SNV dbSNP153 33..33 33 - - - 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_160906,RMVar_hsa_circ_45517,RMVar_hsa_circ_313313,RMVar_hsa_circ_371671,RMVar_hsa_circ_358407,RMVar_hsa_circ_375911,RMVar_hsa_circ_76171,RMVar_hsa_circ_160907,RMVar_hsa_circ_36437,RMVar_hsa_circ_160905 35244 RMVar_ID_35244 Human_SNP_ID_518355453 A-to-I Human chr12 - 121332975 121332975 121332975 TTCTTCTTTTTATTTTTAAAAATATAGAGACAAGGTTTTGCTATGTTGCCCAGGTTGTTCTTGAA TTCTTCTTTTTATTTTTAAAAATATAGAGACAGGGTTTTGCTATGTTGCCCAGGTTGTTCTTGAA T C ANAPC5 Ensembl:ENSG00000089053 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1135180 Functional Loss SNV dbSNP153 33..33 33 - - - 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_160906,RMVar_hsa_circ_45517,RMVar_hsa_circ_313313,RMVar_hsa_circ_371671,RMVar_hsa_circ_358407,RMVar_hsa_circ_375911,RMVar_hsa_circ_76171,RMVar_hsa_circ_160907,RMVar_hsa_circ_36437,RMVar_hsa_circ_160905 35245 RMVar_ID_35245 Human_SNP_ID_518355684 A-to-I Human chr12 - 121334054 121334054 121334054 CCAGGCTGGTTTCAAACTCCTGGCTTCCAGCAATCCTCCCACCTTGGCCTTCCAAAGTGCTGGGA CCAGGCTGGTTTCAAACTCCTGGCTTCCAGCAGTCCTCCCACCTTGGCCTTCCAAAGTGCTGGGA T C ANAPC5 Ensembl:ENSG00000089053 Protein coding intron GSE38233;GSE100210;GSE107867;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank;ASD brains,frontal_cortex - 24183664,29129909,30559470,30559470 RNA-Seq:(High) rs782305483 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17561312 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_160906,RMVar_hsa_circ_45517,RMVar_hsa_circ_313313,RMVar_hsa_circ_371671,RMVar_hsa_circ_358407,RMVar_hsa_circ_375911,RMVar_hsa_circ_76171,RMVar_hsa_circ_160907,RMVar_hsa_circ_36437,RMVar_hsa_circ_160905 35246 RMVar_ID_35246 Human_SNP_ID_518355688 A-to-I Human chr12 - 121334088 121334088 121334088 TATTTTTTGTAGAGGTAGGATCTTGCTTTGTTACCCAGGCTGGTTTCAAACTCCTGGCTTCCAGC TATTTTTTGTAGAGGTAGGATCTTGCTTTGTTGCCCAGGCTGGTTTCAAACTCCTGGCTTCCAGC T C ANAPC5 Ensembl:ENSG00000089053 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1175278066 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11849091,Human_RBP_ID_17561312 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_160906,RMVar_hsa_circ_45517,RMVar_hsa_circ_313313,RMVar_hsa_circ_371671,RMVar_hsa_circ_358407,RMVar_hsa_circ_375911,RMVar_hsa_circ_76171,RMVar_hsa_circ_160907,RMVar_hsa_circ_36437,RMVar_hsa_circ_160905 35247 RMVar_ID_35247 Human_SNP_ID_518355703 A-to-I Human chr12 - 121334161 121334161 121334161 AAGCAGTCCATCTCAGCCTCCTAGCTGTGACTACAGGCATGCACCACAATGCCCAGCTAATTTTT AAGCAGTCCATCTCAGCCTCCTAGCTGTGACTGCAGGCATGCACCACAATGCCCAGCTAATTTTT T C ANAPC5 Ensembl:ENSG00000089053 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs782328332 Functional Loss SNV dbSNP153 33..33 33 - - - 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_160906,RMVar_hsa_circ_45517,RMVar_hsa_circ_313313,RMVar_hsa_circ_371671,RMVar_hsa_circ_358407,RMVar_hsa_circ_375911,RMVar_hsa_circ_76171,RMVar_hsa_circ_160907,RMVar_hsa_circ_36437,RMVar_hsa_circ_160905 35248 RMVar_ID_35248 Human_SNP_ID_518355950 A-to-I Human chr12 - 121335304 121335304 121335304 AAAATTAGCCAGGTGTGGTGGCAGGCACCTGTAGTCCCAGCTACTCAGGAGACTGAGGCAGGAGA AAAATTAGCCAGGTGTGGTGGCAGGCACCTGTTGTCCCAGCTACTCAGGAGACTGAGGCAGGAGA T A ANAPC5 Ensembl:ENSG00000089053 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1042047293 Functional Loss SNV dbSNP153 33..33 33 - - - 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_160906,RMVar_hsa_circ_45517,RMVar_hsa_circ_313313,RMVar_hsa_circ_371671,RMVar_hsa_circ_358407,RMVar_hsa_circ_375911,RMVar_hsa_circ_76171,RMVar_hsa_circ_160907,RMVar_hsa_circ_36437,RMVar_hsa_circ_160905 35249 RMVar_ID_35249 Human_SNP_ID_518355974 A-to-I Human chr12 - 121335441 121335441 121335441 TGCTGTTTGGCCTGGTGCGGTGGCTCACGCCTATAGTCCCAGCACTTTGGGAGGCCAAGGCGGGT TGCTGTTTGGCCTGGTGCGGTGGCTCACGCCTGTAGTCCCAGCACTTTGGGAGGCCAAGGCGGGT T C ANAPC5 Ensembl:ENSG00000089053 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025588604 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11849144,Human_RBP_ID_25019893 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_160906,RMVar_hsa_circ_45517,RMVar_hsa_circ_313313,RMVar_hsa_circ_371671,RMVar_hsa_circ_358407,RMVar_hsa_circ_375911,RMVar_hsa_circ_76171,RMVar_hsa_circ_160907,RMVar_hsa_circ_36437,RMVar_hsa_circ_160905 35250 RMVar_ID_35250 Human_SNP_ID_518356857 A-to-I Human chr12 - 121339227 121339227 121339227 GGCCAACATGGAGAAGCACTGTCTCTACTGAAAATACAAAAAATTAGCCAGATGTGATGGTGGAT GGCCAACATGGAGAAGCACTGTCTCTACTGAATATACAAAAAATTAGCCAGATGTGATGGTGGAT T A ANAPC5 Ensembl:ENSG00000089053 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1486953461 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24940131 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 35251 RMVar_ID_35251 Human_SNP_ID_518359300 A-to-I Human chr12 - 121349438 121349438 121349438 CTCCTACCTCAGTCTTCTAAGTAGCTAGGACTACAGGCACCTGCCACCATGCCTGGCTAATTTTT CTCCTACCTCAGTCTTCTAAGTAGCTAGGACTGCAGGCACCTGCCACCATGCCTGGCTAATTTTT T C ANAPC5 Ensembl:ENSG00000089053 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs972101282 Functional Loss SNV dbSNP153 33..33 33 - - - 35252 RMVar_ID_35252 Human_SNP_ID_518359893 A-to-I Human chr12 - 121351569 121351569 121351569 CCTGTAATTTCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTAGAACCTGGGAAGCGGAGGTT CCTGTAATTTCAGCTACTCGGGAGGCTGAGGCCGGAGAATCGCTAGAACCTGGGAAGCGGAGGTT T G ANAPC5 Ensembl:ENSG00000089053 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs782064195 Functional Loss SNV dbSNP153 33..33 33 - - - 35253 RMVar_ID_35253 Human_SNP_ID_518375416 A-to-I Human chr12 + 121404084 121404084 121404084 GTCGCCAGGCTGGAGTGCAGTGGCACGATCTCAGCTCACTGCAACCTCTGCCTCTCGGGTTCAAA GTCGCCAGGCTGGAGTGCAGTGGCACGATCTCGGCTCACTGCAACCTCTGCCTCTCGGGTTCAAA A G RNF34 Ensembl:ENSG00000170633 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1385005591 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42823,RMVar_hsa_circ_273207,RMVar_hsa_circ_160916 35254 RMVar_ID_35254 Human_SNP_ID_518375453 A-to-I Human chr12 + 121404206 121404206 121404206 TTTCTTCGTATTTAGTAGAGACGGAGTTTCACAATGTTGCCCAGGCTGGTCCCAAACTCCTGAGC TTTCTTCGTATTTAGTAGAGACGGAGTTTCACCATGTTGCCCAGGCTGGTCCCAAACTCCTGAGC A C RNF34 Ensembl:ENSG00000170633 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1417075004 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42823,RMVar_hsa_circ_273207,RMVar_hsa_circ_160916 35255 RMVar_ID_35255 Human_SNP_ID_518380561 A-to-I Human chr12 + 121424530 121424530 121424530 GAGGCTGGAGGAATGCTTGAGCTCACAAGTTCAAGACTAGCTTGGACAACATGGCGAAACCCTGT GAGGCTGGAGGAATGCTTGAGCTCACAAGTTCCAGACTAGCTTGGACAACATGGCGAAACCCTGT A C RNF34 Ensembl:ENSG00000170633 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1449329468 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18619962 35256 RMVar_ID_35256 Human_SNP_ID_518381367 A-to-I Human chr12 - 121427398 121427398 121427398 AGTTGGGACTACAGGTGCCTGCCACCATGCCCAGTTAACTTTTGTATTTTTAGTAGAGATAGGGT AGTTGGGACTACAGGTGCCTGCCACCATGCCCGGTTAACTTTTGTATTTTTAGTAGAGATAGGGT T C lnc-CAMKK2-1 RNACentral:URS00008B65D0 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1359575702 Functional Loss SNV dbSNP153 33..33 33 - - - 35257 RMVar_ID_35257 Human_SNP_ID_518381578 A-to-I Human chr12 + 121428310 121428310 121428310 CGTGTCCTGGGTTCAAGCGATTCTCCTGTCTCAGCCTCCTGAGTAGCTGGGACTACAGGCATGCA CGTGTCCTGGGTTCAAGCGATTCTCCTGTCTCGGCCTCCTGAGTAGCTGGGACTACAGGCATGCA A G RNF34 Ensembl:ENSG00000170633 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs562490516 Functional Loss SNV dbSNP153 33..33 33 - - - 35258 RMVar_ID_35258 Human_SNP_ID_518394578 A-to-I Human chr12 - 121475418 121475418 121475418 TGGCTAAATTTTCTTCTATTTTTTGTAAAGACAGGGTCTCAGTGTGTTGCCCAGGCTGGTCTCAA TGGCTAAATTTTCTTCTATTTTTTGTAAAGACGGGGTCTCAGTGTGTTGCCCAGGCTGGTCTCAA T C KDM2B Ensembl:ENSG00000089094 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1352158186 Functional Loss SNV dbSNP153 33..33 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 35259 RMVar_ID_35259 Human_SNP_ID_518397457 A-to-I Human chr12 - 121486324 121486324 121486324 AAAAAAAAAAAAAAAAAAAAAAAGGAGTTCGAAACCAGCCTGATCAACAAGGTGAAACCCTGTCT AAAAAAAAAAAAAAAAAAAAAAAGGAGTTCGAGACCAGCCTGATCAACAAGGTGAAACCCTGTCT T C KDM2B Ensembl:ENSG00000089094 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1197234310 Functional Loss SNV dbSNP153 33..33 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 35260 RMVar_ID_35260 Human_SNP_ID_518402486 A-to-I Human chr12 - 121506208 121506208 121506208 GAGCCCAGGAGTTTGAGACCAGCCTGGGCAACATAGTAAGACCCTATCTGTACAAAAACAAAAAT GAGCCCAGGAGTTTGAGACCAGCCTGGGCAACGTAGTAAGACCCTATCTGTACAAAAACAAAAAT T C KDM2B Ensembl:ENSG00000089094 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs782110657 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47992,RMVar_hsa_circ_16768,RMVar_hsa_circ_101784,RMVar_hsa_circ_160923,RMVar_hsa_circ_94276,RMVar_hsa_circ_160922,RMVar_hsa_circ_348249,RMVar_hsa_circ_333954,RMVar_hsa_circ_334916,RMVar_hsa_circ_368957,RMVar_hsa_circ_21309,RMVar_hsa_circ_338224,RMVar_hsa_circ_330501 35261 RMVar_ID_35261 Human_SNP_ID_518402502 A-to-I Human chr12 - 121506286 121506286 121506286 GGAGACCCAGAAAAGATTTTGAGGCCTGCTGCAGTGGCTCACACCTGTAATCCTAACATTTTGGA GGAGACCCAGAAAAGATTTTGAGGCCTGCTGCCGTGGCTCACACCTGTAATCCTAACATTTTGGA T G KDM2B Ensembl:ENSG00000089094 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1555302950 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47992,RMVar_hsa_circ_16768,RMVar_hsa_circ_101784,RMVar_hsa_circ_160923,RMVar_hsa_circ_94276,RMVar_hsa_circ_160922,RMVar_hsa_circ_348249,RMVar_hsa_circ_333954,RMVar_hsa_circ_334916,RMVar_hsa_circ_368957,RMVar_hsa_circ_21309,RMVar_hsa_circ_338224,RMVar_hsa_circ_330501 35262 RMVar_ID_35262 Human_SNP_ID_518402977 A-to-I Human chr12 - 121508165 121508165 121508165 AGAGGATTGCTTGACCCCAGAAGGTCACTGCTATAGGGAGCCATGGTCTCGCCACTGCACTCTAG AGAGGATTGCTTGACCCCAGAAGGTCACTGCTGTAGGGAGCCATGGTCTCGCCACTGCACTCTAG T C KDM2B Ensembl:ENSG00000089094 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs782208549 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47992,RMVar_hsa_circ_16768,RMVar_hsa_circ_101784,RMVar_hsa_circ_160923,RMVar_hsa_circ_94276,RMVar_hsa_circ_160922,RMVar_hsa_circ_348249,RMVar_hsa_circ_333954,RMVar_hsa_circ_334916,RMVar_hsa_circ_368957,RMVar_hsa_circ_21309,RMVar_hsa_circ_338224,RMVar_hsa_circ_330501 35263 RMVar_ID_35263 Human_SNP_ID_518403013 A-to-I Human chr12 - 121508360 121508360 121508360 GGGTGCGGGCCAGGCACGGTGGCTCAGGCCTTAATCCCAGCACTTTGGGAAGCTGAGGCAGATGG GGGTGCGGGCCAGGCACGGTGGCTCAGGCCTTCATCCCAGCACTTTGGGAAGCTGAGGCAGATGG T G KDM2B Ensembl:ENSG00000089094 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1177098697 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47992,RMVar_hsa_circ_16768,RMVar_hsa_circ_101784,RMVar_hsa_circ_160923,RMVar_hsa_circ_94276,RMVar_hsa_circ_160922,RMVar_hsa_circ_348249,RMVar_hsa_circ_333954,RMVar_hsa_circ_334916,RMVar_hsa_circ_368957,RMVar_hsa_circ_21309,RMVar_hsa_circ_338224,RMVar_hsa_circ_330501 35264 RMVar_ID_35264 Human_SNP_ID_518413339 A-to-I Human chr12 - 121546511 121546511 121546511 GGGCATGGTGGCGGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGATGTGAA GGGCATGGTGGCGGGCGCCTGTAGTCCCAGCTGCTCGGGAGGCTGAGGCAGGAGAATGATGTGAA T C KDM2B Ensembl:ENSG00000089094 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1428029935 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_113385 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 35265 RMVar_ID_35265 Human_SNP_ID_518413342 A-to-I Human chr12 - 121546521 121546521 121546521 AAAATTAGCCGGGCATGGTGGCGGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTAGCCGGGCATGGTGGCGGGCGCCTGTGGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA T C KDM2B Ensembl:ENSG00000089094 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1422964893 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_113385 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 35266 RMVar_ID_35266 Human_SNP_ID_518423145 A-to-I Human chr12 + 121583478 121583478 121583478 CAGTGACACAATCTCAGCTCACTGCAACCTCCACCTCCTGGACTCAGCAATGCTCCACCTTAGCC CAGTGACACAATCTCAGCTCACTGCAACCTCCGCCTCCTGGACTCAGCAATGCTCCACCTTAGCC A G KDM2B-DT Ensembl:ENSG00000256742 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1201074405 Functional Loss SNV dbSNP153 33..33 33 - - - 35267 RMVar_ID_35267 Human_SNP_ID_518423447 A-to-I Human chr12 + 121585110 121585110 121585110 CCAGCAATTTGGGAGGCCAAGGCGGACAGATCACCTGTGCTCAGGAGTTCGAGACCAGCTTGGGC CCAGCAATTTGGGAGGCCAAGGCGGACAGATCCCCTGTGCTCAGGAGTTCGAGACCAGCTTGGGC A C KDM2B-DT Ensembl:ENSG00000256742 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1220499610 Functional Loss SNV dbSNP153 33..33 33 - - - 35268 RMVar_ID_35268 Human_SNP_ID_518424796 A-to-I Human chr12 + 121590111 121590111 121590111 AAAATTAACCGGGCGTGGTGGCGCGTGCCTGTAATCACAGCTACTAGCGGGGCTGAGGCAGGAAG AAAATTAACCGGGCGTGGTGGCGCGTGCCTGTCATCACAGCTACTAGCGGGGCTGAGGCAGGAAG A C KDM2B-DT Ensembl:ENSG00000256742 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs920406260 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1479800 35269 RMVar_ID_35269 Human_SNP_ID_518425600 A-to-I Human chr12 + 121592840 121592840 121592840 GGAGTCTCACTCTGTCGCCCAGGATGGAGTGCAGTGGTGCGACCTTGGCTCACTGCAACCTCTGC GGAGTCTCACTCTGTCGCCCAGGATGGAGTGCGGTGGTGCGACCTTGGCTCACTGCAACCTCTGC A G KDM2B-DT Ensembl:ENSG00000256742 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1447389385 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_160933 35270 RMVar_ID_35270 Human_SNP_ID_518426914 A-to-I Human chr12 + 121597400 121597400 121597400 TCCTCCCTCTCTGGCTCCCGAAGTGCGGGGATAATAGGCATGAACCACTGTGCACAGCCCATATT TCCTCCCTCTCTGGCTCCCGAAGTGCGGGGATCATAGGCATGAACCACTGTGCACAGCCCATATT A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167552243 Functional Loss SNV dbSNP153 33..33 33 - - - 35271 RMVar_ID_35271 Human_SNP_ID_518426915 A-to-I Human chr12 + 121597400 121597400 121597400 TCCTCCCTCTCTGGCTCCCGAAGTGCGGGGATAATAGGCATGAACCACTGTGCACAGCCCATATT TCCTCCCTCTCTGGCTCCCGAAGTGCGGGGATGATAGGCATGAACCACTGTGCACAGCCCATATT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167552243 Functional Loss SNV dbSNP153 33..33 33 - - - 35272 RMVar_ID_35272 Human_SNP_ID_518462342 A-to-I Human chr12 + 121716782 121716782 121716782 ACAGGGTTTCACCATCTTGGCCAGTCTGGTCTAGAACTCCTGACCTCGTGATCCATCTGCCTTGG ACAGGGTTTCACCATCTTGGCCAGTCTGGTCTGGAACTCCTGACCTCGTGATCCATCTGCCTTGG A G TMEM120B Ensembl:ENSG00000188735 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1390734066 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11850366 RMVar_hsa_circ_91782,RMVar_hsa_circ_100312,RMVar_hsa_circ_160938,RMVar_hsa_circ_160939 35273 RMVar_ID_35273 Human_SNP_ID_518462775 A-to-I Human chr12 + 121718455 121718455 121718455 TTGAACCCAGAAGGCGGAGGTTGCAGTGAGCCAAGATCGTGCCAGGGTACTCCAGCCTGGGTGAC TTGAACCCAGAAGGCGGAGGTTGCAGTGAGCCCAGATCGTGCCAGGGTACTCCAGCCTGGGTGAC A C TMEM120B Ensembl:ENSG00000188735 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1325062047 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91782,RMVar_hsa_circ_100312,RMVar_hsa_circ_160938,RMVar_hsa_circ_160939 35274 RMVar_ID_35274 Human_SNP_ID_518465357 A-to-I Human chr12 + 121728031 121728030 121728032 TTGACACTCACTTTTCTTTTTCCCCCTAAGACAGAGTCTCACTCTGTCGCCCAGGCTAGAGTGCA TTGACACTCACTTTTCTTTTTCCCCCTAAGAC__AGTCTCACTCTGTCGCCCAGGCTAGAGTGCA CAG C TMEM120B Ensembl:ENSG00000188735 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1318061762 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_91782,RMVar_hsa_circ_100312,RMVar_hsa_circ_160938,RMVar_hsa_circ_160939 35275 RMVar_ID_35275 Human_SNP_ID_518466509 A-to-I Human chr12 + 121732026 121732026 121732026 GGGCGTGGTGGCGGGCGCCTGTAGCCCCAGCTACTCGGGAGGCTGAAGCAGTAGAATCTCTTGAA GGGCGTGGTGGCGGGCGCCTGTAGCCCCAGCTGCTCGGGAGGCTGAAGCAGTAGAATCTCTTGAA A G TMEM120B Ensembl:ENSG00000188735 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs970174422 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91782,RMVar_hsa_circ_100312,RMVar_hsa_circ_160938,RMVar_hsa_circ_160939 35276 RMVar_ID_35276 Human_SNP_ID_518466985 A-to-I Human chr12 + 121733806 121733806 121733806 GTGATCCGCCCACCTCGGCCTCCCAAAGTGCTAGGATTACAGGTGTGAGCCACTGCACCTGGCCC GTGATCCGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACTGCACCTGGCCC A G TMEM120B Ensembl:ENSG00000188735 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903532457 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91782,RMVar_hsa_circ_100312,RMVar_hsa_circ_160938,RMVar_hsa_circ_160939 35277 RMVar_ID_35277 Human_SNP_ID_518467218 A-to-I Human chr12 + 121734640 121734640 121734640 TTTACTTCTTTTAAAAAATGGACAGGCTGGGCATGGTGGCTCACACCTGTAATCCCAGCACTTTG TTTACTTCTTTTAAAAAATGGACAGGCTGGGCGTGGTGGCTCACACCTGTAATCCCAGCACTTTG A G TMEM120B Ensembl:ENSG00000188735 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1221368065 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91782,RMVar_hsa_circ_100312,RMVar_hsa_circ_160938,RMVar_hsa_circ_160939 35278 RMVar_ID_35278 Human_SNP_ID_518468401 A-to-I Human chr12 + 121739136 121739136 121739136 TTGAACCCGGGAGGCAGAGGTTGCAGTGAGCCAAGATCGCACCACTGTACTCTGGCCTGGGCGAC TTGAACCCGGGAGGCAGAGGTTGCAGTGAGCCGAGATCGCACCACTGTACTCTGGCCTGGGCGAC A G TMEM120B Ensembl:ENSG00000188735 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs911477940 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91782,RMVar_hsa_circ_100312,RMVar_hsa_circ_160938,RMVar_hsa_circ_160939 35279 RMVar_ID_35279 Human_SNP_ID_518472452 A-to-I Human chr12 + 121752678 121752678 121752678 GGAAGGGTGAGACAGGAGAATCGCTTGAACCCAGGAGGCAGAGGTTGCAGTGAGTTGAGATCGCT GGAAGGGTGAGACAGGAGAATCGCTTGAACCCCGGAGGCAGAGGTTGCAGTGAGTTGAGATCGCT A C TMEM120B Ensembl:ENSG00000188735 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048471591 Functional Loss SNV dbSNP153 33..33 33 - - - 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 35280 RMVar_ID_35280 Human_SNP_ID_518472453 A-to-I Human chr12 + 121752678 121752678 121752678 GGAAGGGTGAGACAGGAGAATCGCTTGAACCCAGGAGGCAGAGGTTGCAGTGAGTTGAGATCGCT GGAAGGGTGAGACAGGAGAATCGCTTGAACCCGGGAGGCAGAGGTTGCAGTGAGTTGAGATCGCT A G TMEM120B Ensembl:ENSG00000188735 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048471591 Functional Loss SNV dbSNP153 33..33 33 - - - 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 35281 RMVar_ID_35281 Human_SNP_ID_518473373 A-to-I Human chr12 + 121756377 121756377 121756377 AAAATTAGTCGGGCCTGATGGCATGCATCTGTAATCCCAGCTACTCGGGAGGCCAAGGCAGGAGA AAAATTAGTCGGGCCTGATGGCATGCATCTGTGATCCCAGCTACTCGGGAGGCCAAGGCAGGAGA A G TMEM120B Ensembl:ENSG00000188735 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1055144036 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11850759 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 35282 RMVar_ID_35282 Human_SNP_ID_518473843 A-to-I Human chr12 + 121758058 121758058 121758058 AGAGGATCGCTTGAGCCCAGGAGATTAAGGCTACAGTGGGCCATGATCACGTCACTGCACTCCAG AGAGGATCGCTTGAGCCCAGGAGATTAAGGCTGCAGTGGGCCATGATCACGTCACTGCACTCCAG A G TMEM120B Ensembl:ENSG00000188735 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1408289984 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24940686 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 35283 RMVar_ID_35283 Human_SNP_ID_518475087 A-to-I Human chr12 + 121762230 121762230 121762230 AGGAGGCAGAGGTTGCAGTGAGCTGAGATCGCACCATTGCACTCCAGCCCAGGGACAATGCAGGA AGGAGGCAGAGGTTGCAGTGAGCTGAGATCGCGCCATTGCACTCCAGCCCAGGGACAATGCAGGA A G TMEM120B Ensembl:ENSG00000188735 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1245902781 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6499,RMVar_hsa_circ_91782,RMVar_hsa_circ_160939,RMVar_hsa_circ_372610,RMVar_hsa_circ_76846,RMVar_hsa_circ_95470,RMVar_hsa_circ_160944,RMVar_hsa_circ_160945,RMVar_hsa_circ_160943,RMVar_hsa_circ_112218,RMVar_hsa_circ_160948,RMVar_hsa_circ_370028,RMVar_hsa_circ_160952 35284 RMVar_ID_35284 Human_SNP_ID_518479668 A-to-I Human chr12 + 121777209 121777209 121777209 TGCCAGGATAGTCTCGATCTCTTGACCTTGTGATCTGCCTGCCTCAGCCTCCCAAAGTGCTGGGA TGCCAGGATAGTCTCGATCTCTTGACCTTGTGTTCTGCCTGCCTCAGCCTCCCAAAGTGCTGGGA A T TMEM120B Ensembl:ENSG00000188735 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs566870332 Functional Loss SNV dbSNP153 33..33 33 - - - 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 35285 RMVar_ID_35285 Human_SNP_ID_518479671 A-to-I Human chr12 + 121777222 121777222 121777222 TCGATCTCTTGACCTTGTGATCTGCCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG TCGATCTCTTGACCTTGTGATCTGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG A G TMEM120B Ensembl:ENSG00000188735 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs73413716 Functional Loss SNV dbSNP153 33..33 33 - - - 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 35286 RMVar_ID_35286 Human_SNP_ID_518479717 A-to-I Human chr12 - 121777410 121777410 121777410 GGGAAATCTCATTTTAAAAATGTAATCAGGCCAGGCACAGTGGCTCACACCTGTAATCCCAGCGC GGGAAATCTCATTTTAAAAATGTAATCAGGCCGGGCACAGTGGCTCACACCTGTAATCCCAGCGC T C lnc-CAMKK2-1 RNACentral:URS00008B65D0 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1210455821 Functional Loss SNV dbSNP153 33..33 33 - - - 35287 RMVar_ID_35287 Human_SNP_ID_518479975 A-to-I Human chr12 - 121778420 121778420 121778420 TTGGGACAGAGTCTCATTCTGTCACTCAGGCTAGAGTGCAGTGGCATGATCTTGGCTCACTGCAA TTGGGACAGAGTCTCATTCTGTCACTCAGGCTGGAGTGCAGTGGCATGATCTTGGCTCACTGCAA T C RHOF Ensembl:ENSG00000139725 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs1190377838 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12075722,Human_RBP_ID_24464403,Human_RBP_ID_26423238 Human_miRNA_ID_112109 35288 RMVar_ID_35288 Human_SNP_ID_518480553 A-to-I Human chr12 + 121780151 121780151 121780151 GCGATCTTGGTTCATCACAACCTCTGCCACCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCG GCGATCTTGGTTCATCACAACCTCTGCCACCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCG A G TMEM120B Ensembl:ENSG00000188735 Protein coding 3'UTR GSE47997;GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831 K562 cells&HepG2 cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line - 23474544,29129909,32596459 RNA-Seq:(High) rs1337610843 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_114767 Human_miRNA_ID_1414404,Human_miRNA_ID_2723955 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 35289 RMVar_ID_35289 Human_SNP_ID_518480555 A-to-I Human chr12 + 121780157 121780157 121780157 TTGGTTCATCACAACCTCTGCCACCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGC TTGGTTCATCACAACCTCTGCCACCCAGGTTCGAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGC A G TMEM120B Ensembl:ENSG00000188735 Protein coding 3'UTR GSE47997;GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490829,GSM3490830,GSM3490831 K562 cells&HepG2 cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,EC109 cell line - 23474544,29129909,32596459,32596459 RNA-Seq:(High) rs561971426 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_114767 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 35290 RMVar_ID_35290 Human_SNP_ID_518480602 A-to-I Human chr12 + 121780319 121780319 121780319 ACCTCAGGTGATTCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTATGC ACCTCAGGTGATTCGCCCGCCTCGGCCTCCCAGAGTGCTGGGATTACAGGCGTGAGCCACTATGC A G TMEM120B Ensembl:ENSG00000188735 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1370081040 Functional Loss SNV dbSNP153 33..33 33 - - - 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 35291 RMVar_ID_35291 Human_SNP_ID_518487323 A-to-I Human chr12 - 121801336 121801336 121801336 AAGACGGGCTTCGCAGCGACCCTCGGGGGTCCATGGAGCCGCCTGCCTTCGCCCCCTCGCTCTTC AAGACGGGCTTCGCAGCGACCCTCGGGGGTCCGTGGAGCCGCCTGCCTTCGCCCCCTCGCTCTTC T C LINC01089,RHOF Ensembl:ENSG00000212694,Ensembl:ENSG00000139725 lincRNA,Protein coding intron,intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs571200612 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_752574 Human_Splice_Rec_1435769 RMVar_hsa_circ_86912,RMVar_hsa_circ_342870,RMVar_hsa_circ_89100,RMVar_hsa_circ_160962,RMVar_hsa_circ_160963,RMVar_hsa_circ_291683,RMVar_hsa_circ_349187,RMVar_hsa_circ_160965 35292 RMVar_ID_35292 Human_SNP_ID_518495563 A-to-I Human chr12 + 121825880 121825880 121825880 GTTGGCCAGGTTGGTCTCGAACTCCTGACCTCAAGTAATTCGCCTGCCTTGGTCTCCCAAACTGC GTTGGCCAGGTTGGTCTCGAACTCCTGACCTCGAGTAATTCGCCTGCCTTGGTCTCCCAAACTGC A G SETD1B Ensembl:ENSG00000139718 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1423303006 Functional Loss SNV dbSNP153 33..33 33 - - - 35293 RMVar_ID_35293 Human_SNP_ID_518503452 A-to-I Human chr12 - 121853456 121853456 121853456 CACCACGCCCGGCTAAATTTTGTATTTTTAGTAGAGGTTTCACCGTGTTATCCAGGATGGTCTCG CACCACGCCCGGCTAAATTTTGTATTTTTAGTGGAGGTTTCACCGTGTTATCCAGGATGGTCTCG T C HPD Ensembl:ENSG00000158104 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1566572509 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11851403 RMVar_hsa_circ_87811,RMVar_hsa_circ_160967,RMVar_hsa_circ_74191,RMVar_hsa_circ_53495,RMVar_hsa_circ_365967 35294 RMVar_ID_35294 Human_SNP_ID_518515986 A-to-I Human chr12 + 121901482 121901481 121901482 GTGATCCTCCTGTCTCAGCCTCCCAAGCAGCTAGGACTGTAGGCACATGTAACCATGCCTGGTTA GTGATCCTCCTGTCTCAGCCTCCCAAGCAGCT_GGACTGTAGGCACATGTAACCATGCCTGGTTA TA T PSMD9,AC069503.2 Ensembl:ENSG00000110801,Ensembl:ENSG00000256950 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs919535136 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_113472,Human_RBP_ID_1267538,Human_RBP_ID_11851546 RMVar_hsa_circ_160970,RMVar_hsa_circ_92659,RMVar_hsa_circ_160971,RMVar_hsa_circ_274514,RMVar_hsa_circ_282670 35295 RMVar_ID_35295 Human_SNP_ID_518517567 A-to-I Human chr12 + 121907455 121907453 121907456 TCACCCAGGCTGGAGTGCAGTGGCATTATCTCAGCTCACTGCAACCTCTGCCTCCCGGCACCTGG TCACCCAGGCTGGAGTGCAGTGGCATTATCT___CTCACTGCAACCTCTGCCTCCCGGCACCTGG TCAG T PSMD9,AC069503.2 Ensembl:ENSG00000110801,Ensembl:ENSG00000256950 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1565894447 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_11851674 35296 RMVar_ID_35296 Human_SNP_ID_518519489 A-to-I Human chr12 + 121914379 121914379 121914379 CAAGACCAGCCTGGCCAACATGGCGAAACCCCATCTCTATTAAAAATACAAAAATTATCTGGGCA CAAGACCAGCCTGGCCAACATGGCGAAACCCCGTCTCTATTAAAAATACAAAAATTATCTGGGCA A G PSMD9,AC069503.2 Ensembl:ENSG00000110801,Ensembl:ENSG00000256950 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs948593815 Functional Loss SNV dbSNP153 33..33 33 - - - 35297 RMVar_ID_35297 Human_SNP_ID_518532547 A-to-I Human chr12 + 121966016 121966016 121966016 TACTATGTTGCCCAGGCTGGACTCGAACTCCTAACCCCAAGCAATCCTCCCACCTTAGCCTCCCA TACTATGTTGCCCAGGCTGGACTCGAACTCCTCACCCCAAGCAATCCTCCCACCTTAGCCTCCCA A C WDR66 Ensembl:ENSG00000158023 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1480966262 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11852454 RMVar_hsa_circ_30358,RMVar_hsa_circ_6965,RMVar_hsa_circ_89230,RMVar_hsa_circ_160974,RMVar_hsa_circ_373043,RMVar_hsa_circ_160979,RMVar_hsa_circ_361413,RMVar_hsa_circ_124999,RMVar_hsa_circ_98002,RMVar_hsa_circ_160982,RMVar_hsa_circ_160983,RMVar_hsa_circ_160980,RMVar_hsa_circ_160981,RMVar_hsa_circ_61810,RMVar_hsa_circ_347267,RMVar_hsa_circ_321211,RMVar_hsa_circ_23648,RMVar_hsa_circ_160992,RMVar_hsa_circ_373066,RMVar_hsa_circ_160994,RMVar_hsa_circ_297728,RMVar_hsa_circ_354298,RMVar_hsa_circ_296449,RMVar_hsa_circ_352677,RMVar_hsa_circ_160995,RMVar_hsa_circ_55052,RMVar_hsa_circ_122327,RMVar_hsa_circ_160996,RMVar_hsa_circ_378853 35298 RMVar_ID_35298 Human_SNP_ID_518537946 A-to-I Human chr12 + 121987553 121987552 121987553 CCTGGCCAACATGGTGAAGCCCTGTCTCTACTAAAAATACAAAAATTAGCCAGGCATGGTGGCGC CCTGGCCAACATGGTGAAGCCCTGTCTCTACT_AAAATACAAAAATTAGCCAGGCATGGTGGCGC TA T WDR66 Ensembl:ENSG00000158023 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1294007106 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_160980 35299 RMVar_ID_35299 Human_SNP_ID_518537947 A-to-I Human chr12 + 121987553 121987553 121987553 CCTGGCCAACATGGTGAAGCCCTGTCTCTACTAAAAATACAAAAATTAGCCAGGCATGGTGGCGC CCTGGCCAACATGGTGAAGCCCTGTCTCTACTGAAAATACAAAAATTAGCCAGGCATGGTGGCGC A G WDR66 Ensembl:ENSG00000158023 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1036664727 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_160980 35300 RMVar_ID_35300 Human_SNP_ID_518537950 A-to-I Human chr12 + 121987572 121987572 121987572 CCCTGTCTCTACTAAAAATACAAAAATTAGCCAGGCATGGTGGCGCACACCTGTAATCCCAGCTA CCCTGTCTCTACTAAAAATACAAAAATTAGCCGGGCATGGTGGCGCACACCTGTAATCCCAGCTA A G WDR66 Ensembl:ENSG00000158023 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs964753326 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_160980 35301 RMVar_ID_35301 Human_SNP_ID_518539119 A-to-I Human chr12 + 121992822 121992822 121992822 GTCTCAAGCTCCTAAAACGATCTACCCACTCCAGCCTCCTAAAGTGCTGGGATTACAGGCGTAAG GTCTCAAGCTCCTAAAACGATCTACCCACTCCGGCCTCCTAAAGTGCTGGGATTACAGGCGTAAG A G WDR66 Ensembl:ENSG00000158023 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992110138 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_160980 35302 RMVar_ID_35302 Human_SNP_ID_518560068 A-to-I Human chr12 + 122069920 122069920 122069920 GTATATGCGTGTGTGTATATTTTTTAAGAGACAAGGTCTTGTTCTGTCATCCAGTCTGGAGTGTA GTATATGCGTGTGTGTATATTTTTTAAGAGACGAGGTCTTGTTCTGTCATCCAGTCTGGAGTGTA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs997879356 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3396255 35303 RMVar_ID_35303 Human_SNP_ID_518560479 A-to-I Human chr12 + 122071463 122071462 122071464 ACAGGAAAATCCTAACTTTTCTTTTTTGAGACAGAGTGTTGCTCTGTCACCCAGGCTGAAGTATA ACAGGAAAATCCTAACTTTTCTTTTTTGAGAC__AGTGTTGCTCTGTCACCCAGGCTGAAGTATA CAG C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1354655864 Functional Loss DEL dbSNP153 33..34 33 - - - 35304 RMVar_ID_35304 Human_SNP_ID_518560536 A-to-I Human chr12 + 122071684 122071684 122071684 CTGATCAACTTCTGACCTCAAATGATCCACCCACCTTGGCCTCCCAAAGTGCTGGGATTATAGGC CTGATCAACTTCTGACCTCAAATGATCCACCCGCCTTGGCCTCCCAAAGTGCTGGGATTATAGGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1363105861 Functional Loss SNV dbSNP153 33..33 33 - - - 35305 RMVar_ID_35305 Human_SNP_ID_518600158 A-to-I Human chr12 - 122210918 122210918 122210918 TCCCCACTTTAGCCTCCCCAGTAGCTGGGATTACAGGTGCACACCACCATGCCCCAGCTAATTTT TCCCCACTTTAGCCTCCCCAGTAGCTGGGATTGCAGGTGCACACCACCATGCCCCAGCTAATTTT T C DIABLO,AC048338.2,AC048338.1 Ensembl:ENSG00000184047,Ensembl:ENSG00000284934,Ensembl:ENSG00000256861 Protein coding,Protein coding,Protein coding intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs976915368 Functional Loss SNV dbSNP153 33..33 33 - - - 35306 RMVar_ID_35306 Human_SNP_ID_518600161 A-to-I Human chr12 - 122210940 122210939 122210940 ACCTCCTGGACTCAAGTGATCCTCCCCACTTTAGCCTCCCCAGTAGCTGGGATTACAGGTGCACA ACCTCCTGGACTCAAGTGATCCTCCCCACTTT_GCCTCCCCAGTAGCTGGGATTACAGGTGCACA CT C DIABLO,AC048338.2,AC048338.1 Ensembl:ENSG00000184047,Ensembl:ENSG00000284934,Ensembl:ENSG00000256861 Protein coding,Protein coding,Protein coding intron,intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1427818960 Functional Loss DEL dbSNP153 33..33 33 - - - 35307 RMVar_ID_35307 Human_SNP_ID_518600532 A-to-I Human chr12 - 122212111 122212111 122212111 CAAAATTGGGCCACGTGCAGTAGTTCACACCTATGATCCCAGCACTTTGGAAGGCCAAGTCAGAT CAAAATTGGGCCACGTGCAGTAGTTCACACCTGTGATCCCAGCACTTTGGAAGGCCAAGTCAGAT T C DIABLO,AC048338.2,AC048338.1 Ensembl:ENSG00000184047,Ensembl:ENSG00000284934,Ensembl:ENSG00000256861 Protein coding,Protein coding,Protein coding intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs896771365 Functional Loss SNV dbSNP153 33..33 33 - - - 35308 RMVar_ID_35308 Human_SNP_ID_518600533 A-to-I Human chr12 - 122212111 122212111 122212111 CAAAATTGGGCCACGTGCAGTAGTTCACACCTATGATCCCAGCACTTTGGAAGGCCAAGTCAGAT CAAAATTGGGCCACGTGCAGTAGTTCACACCTCTGATCCCAGCACTTTGGAAGGCCAAGTCAGAT T G DIABLO,AC048338.2,AC048338.1 Ensembl:ENSG00000184047,Ensembl:ENSG00000284934,Ensembl:ENSG00000256861 Protein coding,Protein coding,Protein coding intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs896771365 Functional Loss SNV dbSNP153 33..33 33 - - - 35309 RMVar_ID_35309 Human_SNP_ID_518600801 A-to-I Human chr12 - 122213059 122213059 122213059 AAAATTAGCCAGGCATGGTGATGGGCGCCTGTAGTCCCAGCTTCTTGGGAGGCTGAGGTGAGAGG AAAATTAGCCAGGCATGGTGATGGGCGCCTGTCGTCCCAGCTTCTTGGGAGGCTGAGGTGAGAGG T G DIABLO,AC048338.2,AC048338.1 Ensembl:ENSG00000184047,Ensembl:ENSG00000284934,Ensembl:ENSG00000256861 Protein coding,Protein coding,Protein coding intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1226570176 Functional Loss SNV dbSNP153 33..33 33 - - - 35310 RMVar_ID_35310 Human_SNP_ID_518600920 A-to-I Human chr12 - 122213416 122213416 122213416 ACTGCTTACTACAGCCTTAGCCTCTGGGCTCAAGCGATCCTACCATGTCAGTCTCCCAGGTAGCT ACTGCTTACTACAGCCTTAGCCTCTGGGCTCAGGCGATCCTACCATGTCAGTCTCCCAGGTAGCT T C DIABLO,AC048338.2,AC048338.1 Ensembl:ENSG00000184047,Ensembl:ENSG00000284934,Ensembl:ENSG00000256861 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1463444985 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6145237,Human_RBP_ID_17811630 35311 RMVar_ID_35311 Human_SNP_ID_518600941 A-to-I Human chr12 - 122213497 122213495 122213498 ACGGAATTTTTTTTTTTTTTTTCCCTGAGACAAGGTCTTACTCTGTTACCAGGCTGGAGTACAGT ACGGAATTTTTTTTTTTTTTTTCCCTGAGAC___GTCTTACTCTGTTACCAGGCTGGAGTACAGT CCTT C DIABLO,AC048338.2,AC048338.1 Ensembl:ENSG00000184047,Ensembl:ENSG00000284934,Ensembl:ENSG00000256861 Protein coding,Protein coding,Protein coding intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1334858036 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_11854324 35312 RMVar_ID_35312 Human_SNP_ID_518601054 A-to-I Human chr12 - 122213828 122213828 122213828 TGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGACATGAGCCACTGCGCTTGGCCCAGAAAA TGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTGCAGACATGAGCCACTGCGCTTGGCCCAGAAAA T C DIABLO,AC048338.2,AC048338.1 Ensembl:ENSG00000184047,Ensembl:ENSG00000284934,Ensembl:ENSG00000256861 Protein coding,Protein coding,Protein coding intron,intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1332800734 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11854346 35313 RMVar_ID_35313 Human_SNP_ID_518601383 A-to-I Human chr12 - 122214873 122214873 122214873 TACCCTGGCCACCGTGGTGAAACCCTGTCTCTACTAAAAATACAAAAATTAGCCAGGTGTAGTGG TACCCTGGCCACCGTGGTGAAACCCTGTCTCTTCTAAAAATACAAAAATTAGCCAGGTGTAGTGG T A DIABLO,AC048338.2,AC048338.1 Ensembl:ENSG00000184047,Ensembl:ENSG00000284934,Ensembl:ENSG00000256861 Protein coding,Protein coding,Protein coding intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1460439111 Functional Loss SNV dbSNP153 33..33 33 - - - 35314 RMVar_ID_35314 Human_SNP_ID_518601384 A-to-I Human chr12 - 122214873 122214873 122214873 TACCCTGGCCACCGTGGTGAAACCCTGTCTCTACTAAAAATACAAAAATTAGCCAGGTGTAGTGG TACCCTGGCCACCGTGGTGAAACCCTGTCTCTGCTAAAAATACAAAAATTAGCCAGGTGTAGTGG T C DIABLO,AC048338.2,AC048338.1 Ensembl:ENSG00000184047,Ensembl:ENSG00000284934,Ensembl:ENSG00000256861 Protein coding,Protein coding,Protein coding intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1460439111 Functional Loss SNV dbSNP153 33..33 33 - - - 35315 RMVar_ID_35315 Human_SNP_ID_518601494 A-to-I Human chr12 - 122215164 122215164 122215164 AATTTTCCTGCCTCAGCCTCCCGATTACAAGCATGCACCACCACGCCTGGCTAATTTTTGTATTT AATTTTCCTGCCTCAGCCTCCCGATTACAAGCGTGCACCACCACGCCTGGCTAATTTTTGTATTT T C DIABLO,AC048338.2,AC048338.1 Ensembl:ENSG00000184047,Ensembl:ENSG00000284934,Ensembl:ENSG00000256861 Protein coding,Protein coding,Protein coding intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs937573186 Functional Loss SNV dbSNP153 33..33 33 - - - 35316 RMVar_ID_35316 Human_SNP_ID_518601495 A-to-I Human chr12 - 122215164 122215164 122215164 AATTTTCCTGCCTCAGCCTCCCGATTACAAGCATGCACCACCACGCCTGGCTAATTTTTGTATTT AATTTTCCTGCCTCAGCCTCCCGATTACAAGCCTGCACCACCACGCCTGGCTAATTTTTGTATTT T G DIABLO,AC048338.2,AC048338.1 Ensembl:ENSG00000184047,Ensembl:ENSG00000284934,Ensembl:ENSG00000256861 Protein coding,Protein coding,Protein coding intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs937573186 Functional Loss SNV dbSNP153 33..33 33 - - - 35317 RMVar_ID_35317 Human_SNP_ID_518603393 A-to-I Human chr12 - 122221563 122221563 122221563 CGAGACCACCCCTCTACAAAAAATAATTAGCTAGGTGTGGTGGCGTGTGTCGGTAGTCCTAGCTA CGAGACCACCCCTCTACAAAAAATAATTAGCTGGGTGTGGTGGCGTGTGTCGGTAGTCCTAGCTA T C DIABLO,AC048338.2,AC048338.1 Ensembl:ENSG00000184047,Ensembl:ENSG00000284934,Ensembl:ENSG00000256861 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1314312915 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_312593,RMVar_hsa_circ_319595,RMVar_hsa_circ_161017,RMVar_hsa_circ_161016,RMVar_hsa_circ_161018,RMVar_hsa_circ_47833,RMVar_hsa_circ_312265 35318 RMVar_ID_35318 Human_SNP_ID_518603404 A-to-I Human chr12 - 122221597 122221596 122221598 GGCCAAGAGTTCGAGACCAGCCTGAGAAACATAGCGAGACCACCCCTCTACAAAAAATAATTAGC GGCCAAGAGTTCGAGACCAGCCTGAGAAACA__GCGAGACCACCCCTCTACAAAAAATAATTAGC CTA C DIABLO,AC048338.2,AC048338.1 Ensembl:ENSG00000184047,Ensembl:ENSG00000284934,Ensembl:ENSG00000256861 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs999440625 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_11854531 RMVar_hsa_circ_312593,RMVar_hsa_circ_319595,RMVar_hsa_circ_161017,RMVar_hsa_circ_161016,RMVar_hsa_circ_161018,RMVar_hsa_circ_47833,RMVar_hsa_circ_312265 35319 RMVar_ID_35319 Human_SNP_ID_518603606 A-to-I Human chr12 - 122222421 122222421 122222421 TTTTTTTGTATTTGTAGTAGGGACAGGGTTTCACCGTGTTAGCCAGGATGGTCTCGATCTCCTGA TTTTTTTGTATTTGTAGTAGGGACAGGGTTTCGCCGTGTTAGCCAGGATGGTCTCGATCTCCTGA T C DIABLO,AC048338.2,AC048338.1 Ensembl:ENSG00000184047,Ensembl:ENSG00000284934,Ensembl:ENSG00000256861 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs958982285 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_312593,RMVar_hsa_circ_319595,RMVar_hsa_circ_161017,RMVar_hsa_circ_161016,RMVar_hsa_circ_161018,RMVar_hsa_circ_47833,RMVar_hsa_circ_312265 35320 RMVar_ID_35320 Human_SNP_ID_518612389 A-to-I Human chr12 - 122253453 122253453 122253453 CACCTCCTGAGTTCAAGTGATTCTGCTGCCTCAGTCACCTGAGTAGCTGGGATTACAGGCACATG CACCTCCTGAGTTCAAGTGATTCTGCTGCCTCGGTCACCTGAGTAGCTGGGATTACAGGCACATG T C VPS33A,AC048338.1 Ensembl:ENSG00000139719,Ensembl:ENSG00000256861 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs528383525 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1436746 RMVar_hsa_circ_161022,RMVar_hsa_circ_363937,RMVar_hsa_circ_41508,RMVar_hsa_circ_126212,RMVar_hsa_circ_161025,RMVar_hsa_circ_161032,RMVar_hsa_circ_366228,RMVar_hsa_circ_161038,RMVar_hsa_circ_105893,RMVar_hsa_circ_161037,RMVar_hsa_circ_121683,RMVar_hsa_circ_161039,RMVar_hsa_circ_265653 35321 RMVar_ID_35321 Human_SNP_ID_518613217 A-to-I Human chr12 - 122256452 122256452 122256452 CTCCCGTCTTAGCTATCCGAGTAGCTGGGATTACAGGAACGCGCCACCACGCCAGGCTAATTTTT CTCCCGTCTTAGCTATCCGAGTAGCTGGGATTGCAGGAACGCGCCACCACGCCAGGCTAATTTTT T C VPS33A,AC048338.1 Ensembl:ENSG00000139719,Ensembl:ENSG00000256861 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs889932395 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_161022,RMVar_hsa_circ_363937,RMVar_hsa_circ_41508,RMVar_hsa_circ_126212,RMVar_hsa_circ_161025,RMVar_hsa_circ_161032,RMVar_hsa_circ_366228,RMVar_hsa_circ_161038,RMVar_hsa_circ_105893,RMVar_hsa_circ_161037,RMVar_hsa_circ_121683,RMVar_hsa_circ_161039,RMVar_hsa_circ_265653 35322 RMVar_ID_35322 Human_SNP_ID_518613775 A-to-I Human chr12 - 122258899 122258899 122258899 TTGGCACACTGCAACCTCGGCCTCCCAGGCTCAAGCAATTCTCCCGCCTCAGCTTCCTGAGTAGA TTGGCACACTGCAACCTCGGCCTCCCAGGCTCGAGCAATTCTCCCGCCTCAGCTTCCTGAGTAGA T C VPS33A,AC048338.1 Ensembl:ENSG00000139719,Ensembl:ENSG00000256861 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1010077216 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_161022,RMVar_hsa_circ_363937,RMVar_hsa_circ_41508,RMVar_hsa_circ_126212,RMVar_hsa_circ_161025,RMVar_hsa_circ_161032,RMVar_hsa_circ_366228,RMVar_hsa_circ_161038,RMVar_hsa_circ_105893,RMVar_hsa_circ_161037,RMVar_hsa_circ_121683,RMVar_hsa_circ_161039,RMVar_hsa_circ_265653 35323 RMVar_ID_35323 Human_SNP_ID_518618422 A-to-I Human chr12 - 122275428 122275428 122275428 TTTTGTATTTTTACTAGAGACAGGGTATCACTATGTTGGCCAGGTTGGTCTTGAACTCCTGACCT TTTTGTATTTTTACTAGAGACAGGGTATCACTGTGTTGGCCAGGTTGGTCTTGAACTCCTGACCT T C CLIP1 Ensembl:ENSG00000130779 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1000239597 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104713,RMVar_hsa_circ_268219,RMVar_hsa_circ_161041,RMVar_hsa_circ_360514,RMVar_hsa_circ_58250 35324 RMVar_ID_35324 Human_SNP_ID_518626216 A-to-I Human chr12 - 122305811 122305811 122305811 CGTCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGCGCTCAGCCATCTGAC CGTCCACCTCAGCCTCCCAAAGTGCTGGGATTGCAGGCATGAGCCACTGCGCTCAGCCATCTGAC T C CLIP1 Ensembl:ENSG00000130779 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1276535070 Functional Loss SNV dbSNP153 33..33 33 - - - 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_58250,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_343361,RMVar_hsa_circ_307810,RMVar_hsa_circ_314558,RMVar_hsa_circ_287261,RMVar_hsa_circ_62040,RMVar_hsa_circ_120675,RMVar_hsa_circ_161046,RMVar_hsa_circ_161047,RMVar_hsa_circ_161043,RMVar_hsa_circ_161044 35325 RMVar_ID_35325 Human_SNP_ID_518626234 A-to-I Human chr12 - 122305871 122305871 122305871 TAGAGACTGGGTTTCATCATGTTGCCCAGGGTAATCTCGAACTCCTGAGCTTAGGCAATCCGTCC TAGAGACTGGGTTTCATCATGTTGCCCAGGGTGATCTCGAACTCCTGAGCTTAGGCAATCCGTCC T C CLIP1 Ensembl:ENSG00000130779 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs925869466 Functional Loss SNV dbSNP153 33..33 33 - - - 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_58250,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_343361,RMVar_hsa_circ_307810,RMVar_hsa_circ_314558,RMVar_hsa_circ_287261,RMVar_hsa_circ_62040,RMVar_hsa_circ_120675,RMVar_hsa_circ_161046,RMVar_hsa_circ_161047,RMVar_hsa_circ_161043,RMVar_hsa_circ_161044 35326 RMVar_ID_35326 Human_SNP_ID_518633946 A-to-I Human chr12 - 122337365 122337365 122337365 CTCGGCTCACCCAACCTCCGCCTCCCAGGCTCAAGCGATTCTTCTGCCTCAGCCTCCCAAGTAGC CTCGGCTCACCCAACCTCCGCCTCCCAGGCTCCAGCGATTCTTCTGCCTCAGCCTCCCAAGTAGC T G CLIP1 Ensembl:ENSG00000130779 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285730669 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12297,RMVar_hsa_circ_28381,RMVar_hsa_circ_104713,RMVar_hsa_circ_161041,RMVar_hsa_circ_360846,RMVar_hsa_circ_31445,RMVar_hsa_circ_161042,RMVar_hsa_circ_367744,RMVar_hsa_circ_372327,RMVar_hsa_circ_307810,RMVar_hsa_circ_314558,RMVar_hsa_circ_62040,RMVar_hsa_circ_161047,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_24428,RMVar_hsa_circ_43368,RMVar_hsa_circ_161051,RMVar_hsa_circ_161052,RMVar_hsa_circ_45437,RMVar_hsa_circ_18786,RMVar_hsa_circ_339671,RMVar_hsa_circ_344769,RMVar_hsa_circ_18285,RMVar_hsa_circ_54738,RMVar_hsa_circ_161055,RMVar_hsa_circ_288729,RMVar_hsa_circ_365477,RMVar_hsa_circ_295142,RMVar_hsa_circ_95273,RMVar_hsa_circ_161056,RMVar_hsa_circ_161057,RMVar_hsa_circ_31890,RMVar_hsa_circ_306965,RMVar_hsa_circ_350331,RMVar_hsa_circ_161058 35327 RMVar_ID_35327 Human_SNP_ID_518634264 A-to-I Human chr12 - 122338499 122338499 122338499 TTGGCCAGGGTGGTCTCGAACTCCTGACCTCAAGTGATCCACTGACCTCGGCCTCCCAAAGTGCT TTGGCCAGGGTGGTCTCGAACTCCTGACCTCAGGTGATCCACTGACCTCGGCCTCCCAAAGTGCT T C CLIP1 Ensembl:ENSG00000130779 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs908173999 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12297,RMVar_hsa_circ_28381,RMVar_hsa_circ_104713,RMVar_hsa_circ_161041,RMVar_hsa_circ_360846,RMVar_hsa_circ_31445,RMVar_hsa_circ_161042,RMVar_hsa_circ_367744,RMVar_hsa_circ_372327,RMVar_hsa_circ_307810,RMVar_hsa_circ_314558,RMVar_hsa_circ_62040,RMVar_hsa_circ_161047,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_24428,RMVar_hsa_circ_43368,RMVar_hsa_circ_161051,RMVar_hsa_circ_161052,RMVar_hsa_circ_45437,RMVar_hsa_circ_18786,RMVar_hsa_circ_339671,RMVar_hsa_circ_344769,RMVar_hsa_circ_18285,RMVar_hsa_circ_54738,RMVar_hsa_circ_161055,RMVar_hsa_circ_288729,RMVar_hsa_circ_365477,RMVar_hsa_circ_295142,RMVar_hsa_circ_95273,RMVar_hsa_circ_161056,RMVar_hsa_circ_161057,RMVar_hsa_circ_31890,RMVar_hsa_circ_306965,RMVar_hsa_circ_350331,RMVar_hsa_circ_161058 35328 RMVar_ID_35328 Human_SNP_ID_518635373 A-to-I Human chr12 - 122342633 122342633 122342633 AAAGACGGGGTCTTGCTGTGTTGCCGAGACTGATCTTGAACTCCTGGCCTCAAGTGATCCTTCTG AAAGACGGGGTCTTGCTGTGTTGCCGAGACTGGTCTTGAACTCCTGGCCTCAAGTGATCCTTCTG T C CLIP1 Ensembl:ENSG00000130779 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1375736545 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12297,RMVar_hsa_circ_28381,RMVar_hsa_circ_104713,RMVar_hsa_circ_161041,RMVar_hsa_circ_360846,RMVar_hsa_circ_31445,RMVar_hsa_circ_161042,RMVar_hsa_circ_367744,RMVar_hsa_circ_307810,RMVar_hsa_circ_314558,RMVar_hsa_circ_62040,RMVar_hsa_circ_357637,RMVar_hsa_circ_72951,RMVar_hsa_circ_364249,RMVar_hsa_circ_24428,RMVar_hsa_circ_43368,RMVar_hsa_circ_161052,RMVar_hsa_circ_18786,RMVar_hsa_circ_339671,RMVar_hsa_circ_18285,RMVar_hsa_circ_54738,RMVar_hsa_circ_161055,RMVar_hsa_circ_288729,RMVar_hsa_circ_365477,RMVar_hsa_circ_31890,RMVar_hsa_circ_350331,RMVar_hsa_circ_33535,RMVar_hsa_circ_324316,RMVar_hsa_circ_349809,RMVar_hsa_circ_161058,RMVar_hsa_circ_329726,RMVar_hsa_circ_279873,RMVar_hsa_circ_33859,RMVar_hsa_circ_39752,RMVar_hsa_circ_161060,RMVar_hsa_circ_161061 35329 RMVar_ID_35329 Human_SNP_ID_518635701 A-to-I Human chr12 - 122344000 122344000 122344000 TTGCCCAGGCTGATCTTGAACTCCTGGCCACAAGTGATCCTCTTGCCTTGGCCTCCCAAAGTGCT TTGCCCAGGCTGATCTTGAACTCCTGGCCACAGGTGATCCTCTTGCCTTGGCCTCCCAAAGTGCT T C CLIP1 Ensembl:ENSG00000130779 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1446887849 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12297,RMVar_hsa_circ_28381,RMVar_hsa_circ_104713,RMVar_hsa_circ_161041,RMVar_hsa_circ_360846,RMVar_hsa_circ_31445,RMVar_hsa_circ_161042,RMVar_hsa_circ_367744,RMVar_hsa_circ_307810,RMVar_hsa_circ_314558,RMVar_hsa_circ_62040,RMVar_hsa_circ_357637,RMVar_hsa_circ_72951,RMVar_hsa_circ_364249,RMVar_hsa_circ_24428,RMVar_hsa_circ_43368,RMVar_hsa_circ_161052,RMVar_hsa_circ_18786,RMVar_hsa_circ_339671,RMVar_hsa_circ_18285,RMVar_hsa_circ_54738,RMVar_hsa_circ_161055,RMVar_hsa_circ_288729,RMVar_hsa_circ_365477,RMVar_hsa_circ_31890,RMVar_hsa_circ_350331,RMVar_hsa_circ_33535,RMVar_hsa_circ_324316,RMVar_hsa_circ_349809,RMVar_hsa_circ_161058,RMVar_hsa_circ_329726,RMVar_hsa_circ_279873,RMVar_hsa_circ_33859,RMVar_hsa_circ_39752,RMVar_hsa_circ_161060,RMVar_hsa_circ_161061 35330 RMVar_ID_35330 Human_SNP_ID_518637971 A-to-I Human chr12 - 122353439 122353439 122353439 GGCTAATTTTTGTAGAGATGGGGTTTTGCCATATTGACCAGGCTGGTCTCAAACTGAACTCAAGC GGCTAATTTTTGTAGAGATGGGGTTTTGCCATGTTGACCAGGCTGGTCTCAAACTGAACTCAAGC T C CLIP1 Ensembl:ENSG00000130779 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1458600788 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12297,RMVar_hsa_circ_28381,RMVar_hsa_circ_104713,RMVar_hsa_circ_161041,RMVar_hsa_circ_360846,RMVar_hsa_circ_31445,RMVar_hsa_circ_161042,RMVar_hsa_circ_367744,RMVar_hsa_circ_307810,RMVar_hsa_circ_314558,RMVar_hsa_circ_357637,RMVar_hsa_circ_72951,RMVar_hsa_circ_364249,RMVar_hsa_circ_24428,RMVar_hsa_circ_161052,RMVar_hsa_circ_11372,RMVar_hsa_circ_18285,RMVar_hsa_circ_54738,RMVar_hsa_circ_288729,RMVar_hsa_circ_365477,RMVar_hsa_circ_31890,RMVar_hsa_circ_33535,RMVar_hsa_circ_324316,RMVar_hsa_circ_329726,RMVar_hsa_circ_33859,RMVar_hsa_circ_39752,RMVar_hsa_circ_161061,RMVar_hsa_circ_31080,RMVar_hsa_circ_299332,RMVar_hsa_circ_310583,RMVar_hsa_circ_161062,RMVar_hsa_circ_303021,RMVar_hsa_circ_294560,RMVar_hsa_circ_161064,RMVar_hsa_circ_161065,RMVar_hsa_circ_161066,RMVar_hsa_circ_161063 35331 RMVar_ID_35331 Human_SNP_ID_518640613 A-to-I Human chr12 - 122361718 122361718 122361718 CAAGAGAGCCTCCTGCACCACCATGCCTGGCTAGTTTTTGTATTTTTTGTAGAGACGGGGTCTGT CAAGAGAGCCTCCTGCACCACCATGCCTGGCTGGTTTTTGTATTTTTTGTAGAGACGGGGTCTGT T C CLIP1 Ensembl:ENSG00000130779 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1201362246 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12075959 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_31080,RMVar_hsa_circ_294560,RMVar_hsa_circ_161066,RMVar_hsa_circ_161069,RMVar_hsa_circ_289502,RMVar_hsa_circ_307778,RMVar_hsa_circ_161068 35332 RMVar_ID_35332 Human_SNP_ID_518646360 A-to-I Human chr12 - 122385038 122385038 122385038 GTCCCAGCTACTCATGAGTCTGAGGCAGGAGAATCGCTTGAACCTGGGAGGCAGAGGTCGCAGAG GTCCCAGCTACTCATGAGTCTGAGGCAGGAGATTCGCTTGAACCTGGGAGGCAGAGGTCGCAGAG T A CLIP1 Ensembl:ENSG00000130779 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs182424095 Functional Loss SNV dbSNP153 33..33 33 - - - 35333 RMVar_ID_35333 Human_SNP_ID_518651718 A-to-I Human chr12 - 122404386 122404386 122404386 CATGTTGGCCAGCCCGAAGGTCTCGAACTCCTAGCCTCAAGTGATTTACCCACCTTGGCCTCCCA CATGTTGGCCAGCCCGAAGGTCTCGAACTCCTGGCCTCAAGTGATTTACCCACCTTGGCCTCCCA T C CLIP1 Ensembl:ENSG00000130779 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1161204485 Functional Loss SNV dbSNP153 33..33 33 - - - 35334 RMVar_ID_35334 Human_SNP_ID_518652277 A-to-I Human chr12 - 122406243 122406243 122406243 CAGGGTTTCGCCATGTTTCCTAGGATGATCTCAAACTCCTGAGCTCAAAACTATCTGCCCACCTT CAGGGTTTCGCCATGTTTCCTAGGATGATCTCGAACTCCTGAGCTCAAAACTATCTGCCCACCTT T C CLIP1 Ensembl:ENSG00000130779 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355157480 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11855918 35335 RMVar_ID_35335 Human_SNP_ID_518653799 A-to-I Human chr12 - 122412246 122412246 122412246 AGCTCAGGGCAACATGGCAAAACTCCATTTCTACAAAAACAAAAGTTAGCCAGGGATGGTTGTGT AGCTCAGGGCAACATGGCAAAACTCCATTTCTGCAAAAACAAAAGTTAGCCAGGGATGGTTGTGT T C CLIP1 Ensembl:ENSG00000130779 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1425053240 Functional Loss SNV dbSNP153 33..33 33 - - - 35336 RMVar_ID_35336 Human_SNP_ID_518653815 A-to-I Human chr12 - 122412313 122412313 122412313 GGCCAGGTGTGGTGGCTCACCCCTGTAATCCCAGCACTTTGGGAGGCTGAAGTGGATGGATCCCG GGCCAGGTGTGGTGGCTCACCCCTGTAATCCCGGCACTTTGGGAGGCTGAAGTGGATGGATCCCG T C CLIP1 Ensembl:ENSG00000130779 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1373079706 Functional Loss SNV dbSNP153 33..33 33 - - - 35337 RMVar_ID_35337 Human_SNP_ID_518655937 A-to-I Human chr12 - 122420835 122420835 122420835 GGCCTCCCAGGTTTAAGCGATTCTCGTGCCTCAGCCTCCTGAGTACTGGAATTACAGGTGCCCGC GGCCTCCCAGGTTTAAGCGATTCTCGTGCCTCGGCCTCCTGAGTACTGGAATTACAGGTGCCCGC T C CLIP1 Ensembl:ENSG00000130779 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1463405555 Functional Loss SNV dbSNP153 33..33 33 - - - 35338 RMVar_ID_35338 Human_SNP_ID_518670241 A-to-I Human chr12 - 122472517 122472511 122472517 CCTGGCCGGTGCATATAACTTTTAAGTTTAAAAGTAAATTGTTGGCCAGGCGTGGTGGCTCATGC CCTGGCCGGTGCATATAACTTTTAAGTTTAAA______TTGTTGGCCAGGCGTGGTGGCTCATGC ATTTACT A ZCCHC8 Ensembl:ENSG00000033030 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893296119 Functional Loss DEL dbSNP153 33..38 33 - - - 35339 RMVar_ID_35339 Human_SNP_ID_518670959 A-to-I Human chr12 - 122475159 122475128 122475160 GCTGTAATCCCAGCTACTTGGGAGGCAGAGGCAGAAGAACTGCTTGAACCCGGGAGGCAGAGGTT GCTGTAATCCCAGCTACTTGGGAGGCAGAGG________________________________TT ACCTCTGCCTCCCGGGTTCAAGCAGTTCTTCTG A ZCCHC8 Ensembl:ENSG00000033030 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1315253858 Functional Loss DEL dbSNP153 32..63 33 - - - 35340 RMVar_ID_35340 Human_SNP_ID_518670965 A-to-I Human chr12 - 122475159 122475159 122475159 GCTGTAATCCCAGCTACTTGGGAGGCAGAGGCAGAAGAACTGCTTGAACCCGGGAGGCAGAGGTT GCTGTAATCCCAGCTACTTGGGAGGCAGAGGCGGAAGAACTGCTTGAACCCGGGAGGCAGAGGTT T C ZCCHC8 Ensembl:ENSG00000033030 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1187452048 Functional Loss SNV dbSNP153 33..33 33 - - - 35341 RMVar_ID_35341 Human_SNP_ID_518673076 A-to-I Human chr12 - 122484190 122484190 122484190 TTCTCAGGAGGCTGAGGTGGGAGGATCGTTTGAGCCTGGCAGGTGGAGGTTGCAGTAAGCCAAGA TTCTCAGGAGGCTGAGGTGGGAGGATCGTTTGCGCCTGGCAGGTGGAGGTTGCAGTAAGCCAAGA T G ZCCHC8 Ensembl:ENSG00000033030 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202224720 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23543902 RMVar_hsa_circ_67141,RMVar_hsa_circ_27111,RMVar_hsa_circ_161075,RMVar_hsa_circ_69295 35342 RMVar_ID_35342 Human_SNP_ID_518673544 A-to-I Human chr12 - 122486366 122486366 122486366 CTCTGTCACCCAGGCTAGAGTGCCATGGCACAATCTCAGCTTACTGCAACCTCCCCCTCCCAGAT CTCTGTCACCCAGGCTAGAGTGCCATGGCACAGTCTCAGCTTACTGCAACCTCCCCCTCCCAGAT T C ZCCHC8 Ensembl:ENSG00000033030 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1222476273 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11856362 RMVar_hsa_circ_67141,RMVar_hsa_circ_27111,RMVar_hsa_circ_161075,RMVar_hsa_circ_69295 35343 RMVar_ID_35343 Human_SNP_ID_518673549 A-to-I Human chr12 - 122486382 122486382 122486382 TTGAGACAGCCTCTCGCTCTGTCACCCAGGCTAGAGTGCCATGGCACAATCTCAGCTTACTGCAA TTGAGACAGCCTCTCGCTCTGTCACCCAGGCTGGAGTGCCATGGCACAATCTCAGCTTACTGCAA T C ZCCHC8 Ensembl:ENSG00000033030 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1235100812 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11856362 RMVar_hsa_circ_67141,RMVar_hsa_circ_27111,RMVar_hsa_circ_161075,RMVar_hsa_circ_69295 35344 RMVar_ID_35344 Human_SNP_ID_518673561 A-to-I Human chr12 - 122486411 122486410 122486411 TTGACTTTTTTTTTTTTTTTTTTTTTTTTTTGAGACAGCCTCTCGCTCTGTCACCCAGGCTAGAG TTGACTTTTTTTTTTTTTTTTTTTTTTTTTTG_GACAGCCTCTCGCTCTGTCACCCAGGCTAGAG CT C ZCCHC8 Ensembl:ENSG00000033030 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1381273089 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_2309981,Human_RBP_ID_11856363 RMVar_hsa_circ_67141,RMVar_hsa_circ_27111,RMVar_hsa_circ_161075,RMVar_hsa_circ_69295 35345 RMVar_ID_35345 Human_SNP_ID_518673950 A-to-I Human chr12 - 122488122 122488122 122488122 GAGACTGAGTCACGGAAATTGCTTTGAACCCAAGAGACTGAGGCTGCAGTGAGCCGAGATTTGCC GAGACTGAGTCACGGAAATTGCTTTGAACCCAGGAGACTGAGGCTGCAGTGAGCCGAGATTTGCC T C ZCCHC8 Ensembl:ENSG00000033030 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs545677205 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67141,RMVar_hsa_circ_27111,RMVar_hsa_circ_161075,RMVar_hsa_circ_69295 35346 RMVar_ID_35346 Human_SNP_ID_518674059 A-to-I Human chr12 - 122488691 122488691 122488691 AATTTTTGTATTTTTAGTAGGGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGA AATTTTTGTATTTTTAGTAGGGACAGGGTTTCCCCATGTTGGCCAGGCTGGTCTCGAACTCCTGA T G ZCCHC8 Ensembl:ENSG00000033030 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs142162932 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67141,RMVar_hsa_circ_27111,RMVar_hsa_circ_161075,RMVar_hsa_circ_69295 35347 RMVar_ID_35347 Human_SNP_ID_518678626 A-to-I Human chr12 - 122505877 122505877 122505877 CTATTTGGGAGGCTGAGGCATAAGAATTACTTAAACCCAGGAGGCAGAGGTTGCAGTGAGCCGAG CTATTTGGGAGGCTGAGGCATAAGAATTACTTCAACCCAGGAGGCAGAGGTTGCAGTGAGCCGAG T G RSRC2 Ensembl:ENSG00000111011 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1046608620 Functional Loss SNV dbSNP153 33..33 33 - - - 35348 RMVar_ID_35348 Human_SNP_ID_518678629 A-to-I Human chr12 - 122505881 122505881 122505881 CCAGCTATTTGGGAGGCTGAGGCATAAGAATTACTTAAACCCAGGAGGCAGAGGTTGCAGTGAGC CCAGCTATTTGGGAGGCTGAGGCATAAGAATTCCTTAAACCCAGGAGGCAGAGGTTGCAGTGAGC T G RSRC2 Ensembl:ENSG00000111011 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1358080038 Functional Loss SNV dbSNP153 33..33 33 - - - 35349 RMVar_ID_35349 Human_SNP_ID_518679088 A-to-I Human chr12 - 122507231 122507231 122507231 GGGTCTACAGGTGCCCACCACCATGCCAGGCTAGTTTTTTGTATTTTTAGTAGAGACGGGGTTTC GGGTCTACAGGTGCCCACCACCATGCCAGGCTGGTTTTTTGTATTTTTAGTAGAGACGGGGTTTC T C RSRC2 Ensembl:ENSG00000111011 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1173398004 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11856800 Human_Splice_Rec_1437444 RMVar_hsa_circ_55503,RMVar_hsa_circ_327177,RMVar_hsa_circ_66156 35350 RMVar_ID_35350 Human_SNP_ID_518679094 A-to-I Human chr12 - 122507257 122507257 122507257 CTGCCTCAGACTCCTGAGACCCTCCTGGGTCTACAGGTGCCCACCACCATGCCAGGCTAGTTTTT CTGCCTCAGACTCCTGAGACCCTCCTGGGTCTGCAGGTGCCCACCACCATGCCAGGCTAGTTTTT T C RSRC2 Ensembl:ENSG00000111011 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs564107368 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55503,RMVar_hsa_circ_327177,RMVar_hsa_circ_66156 35351 RMVar_ID_35351 Human_SNP_ID_518679371 A-to-I Human chr12 - 122508054 122508054 122508054 TTATGCCTTTAATCCCAGCACTTTGGGATGCCAAGTGAGCGGATCAGTTGAGGTAAGGAGTCCAA TTATGCCTTTAATCCCAGCACTTTGGGATGCCTAGTGAGCGGATCAGTTGAGGTAAGGAGTCCAA T A RSRC2 Ensembl:ENSG00000111011 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs553058943 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19061659,Human_RBP_ID_24408180 RMVar_hsa_circ_55503,RMVar_hsa_circ_327177,RMVar_hsa_circ_66156 35352 RMVar_ID_35352 Human_SNP_ID_518680029 A-to-I Human chr12 - 122509962 122509962 122509962 CAAAAATTAGCCAGGCGTGGTTGTGTGTGCCTATAGTCCCAGCTACTCAGGAGGCTTGAACTCGG CAAAAATTAGCCAGGCGTGGTTGTGTGTGCCTGTAGTCCCAGCTACTCAGGAGGCTTGAACTCGG T C RSRC2 Ensembl:ENSG00000111011 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs777591321 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_327177,RMVar_hsa_circ_66156,RMVar_hsa_circ_304157,RMVar_hsa_circ_324267,RMVar_hsa_circ_356319,RMVar_hsa_circ_161081,RMVar_hsa_circ_161082 35353 RMVar_ID_35353 Human_SNP_ID_518680624 A-to-I Human chr12 - 122511935 122511935 122511935 GGGCATGGTGGTGTGTACCTGTAATCCCGGCTACACAGGAGGCTGAGGCAGGAGAATCGCTTGAA GGGCATGGTGGTGTGTACCTGTAATCCCGGCTGCACAGGAGGCTGAGGCAGGAGAATCGCTTGAA T C RSRC2 Ensembl:ENSG00000111011 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs140316716 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17561319 RMVar_hsa_circ_66156,RMVar_hsa_circ_324267,RMVar_hsa_circ_356319,RMVar_hsa_circ_161082,RMVar_hsa_circ_277407,RMVar_hsa_circ_161083 35354 RMVar_ID_35354 Human_SNP_ID_518680815 A-to-I Human chr12 - 122512568 122512568 122512568 ACCACCACGCCCTGCTAATTTTTTGTATTTTTAGTAGATGCGGGATTTCACCATGTTAATAACCA ACCACCACGCCCTGCTAATTTTTTGTATTTTTTGTAGATGCGGGATTTCACCATGTTAATAACCA T A RSRC2 Ensembl:ENSG00000111011 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1009849930 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11856941 RMVar_hsa_circ_66156,RMVar_hsa_circ_324267,RMVar_hsa_circ_356319,RMVar_hsa_circ_161082,RMVar_hsa_circ_277407,RMVar_hsa_circ_161083 35355 RMVar_ID_35355 Human_SNP_ID_518680818 A-to-I Human chr12 - 122512584 122512584 122512584 GAGATTACAGGCGCCCACCACCACGCCCTGCTAATTTTTTGTATTTTTAGTAGATGCGGGATTTC GAGATTACAGGCGCCCACCACCACGCCCTGCTGATTTTTTGTATTTTTAGTAGATGCGGGATTTC T C RSRC2 Ensembl:ENSG00000111011 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1292406616 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11856941,Human_RBP_ID_24942249 RMVar_hsa_circ_66156,RMVar_hsa_circ_324267,RMVar_hsa_circ_356319,RMVar_hsa_circ_161082,RMVar_hsa_circ_277407,RMVar_hsa_circ_161083 35356 RMVar_ID_35356 Human_SNP_ID_518680848 A-to-I Human chr12 - 122512680 122512680 122512680 TTGCCTAGGCTGGAGTGCAGTGGTGTGATCTCAGCTTACTGCAACCCCTGCCTCCTGGGTTCAAG TTGCCTAGGCTGGAGTGCAGTGGTGTGATCTCGGCTTACTGCAACCCCTGCCTCCTGGGTTCAAG T C RSRC2 Ensembl:ENSG00000111011 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs984765639 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66156,RMVar_hsa_circ_324267,RMVar_hsa_circ_356319,RMVar_hsa_circ_161082,RMVar_hsa_circ_277407,RMVar_hsa_circ_161083 35357 RMVar_ID_35357 Human_SNP_ID_518681325 A-to-I Human chr12 - 122514020 122514019 122514020 TTACAAAATTAAGGTGTTTTGTTTTTTGAGACAGGGTCCCACCCAGGCTGGAGTGCAGTGGCACA TTACAAAATTAAGGTGTTTTGTTTTTTGAGAC_GGGTCCCACCCAGGCTGGAGTGCAGTGGCACA CT C RSRC2 Ensembl:ENSG00000111011 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1177038770 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_754601,Human_RBP_ID_6146085,Human_RBP_ID_11856973 RMVar_hsa_circ_66156,RMVar_hsa_circ_324267,RMVar_hsa_circ_356319,RMVar_hsa_circ_161082,RMVar_hsa_circ_277407,RMVar_hsa_circ_161083 35358 RMVar_ID_35358 Human_SNP_ID_518681326 A-to-I Human chr12 - 122514020 122514020 122514020 TTACAAAATTAAGGTGTTTTGTTTTTTGAGACAGGGTCCCACCCAGGCTGGAGTGCAGTGGCACA TTACAAAATTAAGGTGTTTTGTTTTTTGAGACGGGGTCCCACCCAGGCTGGAGTGCAGTGGCACA T C RSRC2 Ensembl:ENSG00000111011 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1439362701 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_754601,Human_RBP_ID_6146085,Human_RBP_ID_11856973 RMVar_hsa_circ_66156,RMVar_hsa_circ_324267,RMVar_hsa_circ_356319,RMVar_hsa_circ_161082,RMVar_hsa_circ_277407,RMVar_hsa_circ_161083 35359 RMVar_ID_35359 Human_SNP_ID_518682367 A-to-I Human chr12 - 122516975 122516975 122516975 TGAATAGGCCTATTAAAATGCAGTTGTTGGCTAGGTGTCGTGGTTTACACCTGTAATCACAACGA TGAATAGGCCTATTAAAATGCAGTTGTTGGCTGGGTGTCGTGGTTTACACCTGTAATCACAACGA T C RSRC2 Ensembl:ENSG00000111011 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1401108831 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11857062 RMVar_hsa_circ_72827,RMVar_hsa_circ_356319,RMVar_hsa_circ_367831,RMVar_hsa_circ_56997 35360 RMVar_ID_35360 Human_SNP_ID_518688041 A-to-I Human chr12 + 122535771 122535771 122535771 CCAGGAGGCAGAGGTTGCAGTGAGCCAAGATTATGCCACTATACTCTAGCCTGAGTGACAGAGTG CCAGGAGGCAGAGGTTGCAGTGAGCCAAGATTGTGCCACTATACTCTAGCCTGAGTGACAGAGTG A G KNTC1 Ensembl:ENSG00000184445 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1379113380 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10223,RMVar_hsa_circ_105901,RMVar_hsa_circ_107161,RMVar_hsa_circ_124960,RMVar_hsa_circ_161088,RMVar_hsa_circ_121846,RMVar_hsa_circ_109285,RMVar_hsa_circ_161089,RMVar_hsa_circ_161090,RMVar_hsa_circ_161091,RMVar_hsa_circ_334725,RMVar_hsa_circ_363705,RMVar_hsa_circ_364078,RMVar_hsa_circ_378232,RMVar_hsa_circ_124033,RMVar_hsa_circ_81914,RMVar_hsa_circ_97580,RMVar_hsa_circ_69005,RMVar_hsa_circ_161092,RMVar_hsa_circ_161094,RMVar_hsa_circ_161095,RMVar_hsa_circ_161096,RMVar_hsa_circ_161093 35361 RMVar_ID_35361 Human_SNP_ID_518688609 A-to-I Human chr12 + 122537987 122537987 122537987 AAACCTCGTCTGTACAAAAAATACCAAAAACTAGCTGGCCATAGTGGTGTGTACCTGTGGTCCCA AAACCTCGTCTGTACAAAAAATACCAAAAACTGGCTGGCCATAGTGGTGTGTACCTGTGGTCCCA A G KNTC1 Ensembl:ENSG00000184445 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1380093155 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10223,RMVar_hsa_circ_105901,RMVar_hsa_circ_107161,RMVar_hsa_circ_124960,RMVar_hsa_circ_161088,RMVar_hsa_circ_121846,RMVar_hsa_circ_109285,RMVar_hsa_circ_161089,RMVar_hsa_circ_161090,RMVar_hsa_circ_161091,RMVar_hsa_circ_334725,RMVar_hsa_circ_363705,RMVar_hsa_circ_364078,RMVar_hsa_circ_378232,RMVar_hsa_circ_124033,RMVar_hsa_circ_81914,RMVar_hsa_circ_97580,RMVar_hsa_circ_69005,RMVar_hsa_circ_161092,RMVar_hsa_circ_161094,RMVar_hsa_circ_161095,RMVar_hsa_circ_161096,RMVar_hsa_circ_161093 35362 RMVar_ID_35362 Human_SNP_ID_518689356 A-to-I Human chr12 + 122540989 122540988 122540990 GTCTAGGAGCTCGAAACCAGCCTGGATAATATAGAGAGACCGCCACCTCTACAAAAAATAAAAAA GTCTAGGAGCTCGAAACCAGCCTGGATAATAT__AGAGACCGCCACCTCTACAAAAAATAAAAAA TAG T KNTC1 Ensembl:ENSG00000184445 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1446927539 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_10223,RMVar_hsa_circ_105901,RMVar_hsa_circ_107161,RMVar_hsa_circ_124960,RMVar_hsa_circ_161088,RMVar_hsa_circ_109285,RMVar_hsa_circ_161090,RMVar_hsa_circ_161091,RMVar_hsa_circ_363705,RMVar_hsa_circ_378232,RMVar_hsa_circ_124033,RMVar_hsa_circ_81914,RMVar_hsa_circ_97580,RMVar_hsa_circ_69005,RMVar_hsa_circ_116321,RMVar_hsa_circ_161092,RMVar_hsa_circ_161094,RMVar_hsa_circ_161095,RMVar_hsa_circ_161096,RMVar_hsa_circ_161093,RMVar_hsa_circ_161098,RMVar_hsa_circ_92703,RMVar_hsa_circ_161101,RMVar_hsa_circ_108321,RMVar_hsa_circ_111263,RMVar_hsa_circ_98991,RMVar_hsa_circ_161102,RMVar_hsa_circ_161099,RMVar_hsa_circ_161100 35363 RMVar_ID_35363 Human_SNP_ID_518689370 A-to-I Human chr12 + 122541024 122541024 122541024 GAGACCGCCACCTCTACAAAAAATAAAAAATTAGCCACATGTGTTGGTGTGTGTCTGTAGTCCCA GAGACCGCCACCTCTACAAAAAATAAAAAATTGGCCACATGTGTTGGTGTGTGTCTGTAGTCCCA A G KNTC1 Ensembl:ENSG00000184445 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1407717003 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10223,RMVar_hsa_circ_105901,RMVar_hsa_circ_107161,RMVar_hsa_circ_124960,RMVar_hsa_circ_161088,RMVar_hsa_circ_109285,RMVar_hsa_circ_161090,RMVar_hsa_circ_161091,RMVar_hsa_circ_363705,RMVar_hsa_circ_378232,RMVar_hsa_circ_124033,RMVar_hsa_circ_81914,RMVar_hsa_circ_97580,RMVar_hsa_circ_69005,RMVar_hsa_circ_116321,RMVar_hsa_circ_161092,RMVar_hsa_circ_161094,RMVar_hsa_circ_161095,RMVar_hsa_circ_161096,RMVar_hsa_circ_161093,RMVar_hsa_circ_161098,RMVar_hsa_circ_92703,RMVar_hsa_circ_161101,RMVar_hsa_circ_108321,RMVar_hsa_circ_111263,RMVar_hsa_circ_98991,RMVar_hsa_circ_161102,RMVar_hsa_circ_161099,RMVar_hsa_circ_161100 35364 RMVar_ID_35364 Human_SNP_ID_518694379 A-to-I Human chr12 + 122558804 122558804 122558804 AGGCTGAGGCATGAGAATTGCTTGAACCTGGTAGGCAGAGGTTAGGGTGAGCCAAAACTGCGCCA AGGCTGAGGCATGAGAATTGCTTGAACCTGGTGGGCAGAGGTTAGGGTGAGCCAAAACTGCGCCA A G KNTC1 Ensembl:ENSG00000184445 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1565954510 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107161,RMVar_hsa_circ_124960,RMVar_hsa_circ_161088,RMVar_hsa_circ_161091,RMVar_hsa_circ_378232,RMVar_hsa_circ_124033,RMVar_hsa_circ_81914,RMVar_hsa_circ_97580,RMVar_hsa_circ_5726,RMVar_hsa_circ_95867,RMVar_hsa_circ_161094,RMVar_hsa_circ_161095,RMVar_hsa_circ_161096,RMVar_hsa_circ_161093,RMVar_hsa_circ_161098,RMVar_hsa_circ_92703,RMVar_hsa_circ_161101,RMVar_hsa_circ_108321,RMVar_hsa_circ_111263,RMVar_hsa_circ_98991,RMVar_hsa_circ_161099,RMVar_hsa_circ_161100,RMVar_hsa_circ_112227,RMVar_hsa_circ_6652,RMVar_hsa_circ_161104,RMVar_hsa_circ_161105,RMVar_hsa_circ_50545,RMVar_hsa_circ_106319,RMVar_hsa_circ_71486,RMVar_hsa_circ_161108,RMVar_hsa_circ_161109,RMVar_hsa_circ_346904,RMVar_hsa_circ_376574,RMVar_hsa_circ_100924,RMVar_hsa_circ_49905,RMVar_hsa_circ_161113,RMVar_hsa_circ_96683,RMVar_hsa_circ_16878,RMVar_hsa_circ_161115,RMVar_hsa_circ_105638,RMVar_hsa_circ_320660,RMVar_hsa_circ_372340,RMVar_hsa_circ_161116,RMVar_hsa_circ_4115,RMVar_hsa_circ_161117,RMVar_hsa_circ_358681,RMVar_hsa_circ_25523,RMVar_hsa_circ_112565,RMVar_hsa_circ_161118,RMVar_hsa_circ_45216,RMVar_hsa_circ_161120,RMVar_hsa_circ_113421,RMVar_hsa_circ_161121,RMVar_hsa_circ_161122,RMVar_hsa_circ_342529 35365 RMVar_ID_35365 Human_SNP_ID_518694622 A-to-I Human chr12 + 122559750 122559750 122559750 TCCCGCTGCCACCACACCTGGCTAATTTTTGTATTTTAGTAGAGACGGAGTTTCACCATGTTGGT TCCCGCTGCCACCACACCTGGCTAATTTTTGTGTTTTAGTAGAGACGGAGTTTCACCATGTTGGT A G KNTC1 Ensembl:ENSG00000184445 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs925859805 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107161,RMVar_hsa_circ_124960,RMVar_hsa_circ_161088,RMVar_hsa_circ_161091,RMVar_hsa_circ_378232,RMVar_hsa_circ_124033,RMVar_hsa_circ_81914,RMVar_hsa_circ_97580,RMVar_hsa_circ_5726,RMVar_hsa_circ_95867,RMVar_hsa_circ_161094,RMVar_hsa_circ_161095,RMVar_hsa_circ_161096,RMVar_hsa_circ_161093,RMVar_hsa_circ_161098,RMVar_hsa_circ_92703,RMVar_hsa_circ_161101,RMVar_hsa_circ_108321,RMVar_hsa_circ_111263,RMVar_hsa_circ_98991,RMVar_hsa_circ_161099,RMVar_hsa_circ_161100,RMVar_hsa_circ_112227,RMVar_hsa_circ_6652,RMVar_hsa_circ_161104,RMVar_hsa_circ_161105,RMVar_hsa_circ_50545,RMVar_hsa_circ_106319,RMVar_hsa_circ_71486,RMVar_hsa_circ_161108,RMVar_hsa_circ_161109,RMVar_hsa_circ_346904,RMVar_hsa_circ_376574,RMVar_hsa_circ_100924,RMVar_hsa_circ_49905,RMVar_hsa_circ_161113,RMVar_hsa_circ_96683,RMVar_hsa_circ_16878,RMVar_hsa_circ_161115,RMVar_hsa_circ_105638,RMVar_hsa_circ_320660,RMVar_hsa_circ_372340,RMVar_hsa_circ_161116,RMVar_hsa_circ_4115,RMVar_hsa_circ_161117,RMVar_hsa_circ_358681,RMVar_hsa_circ_25523,RMVar_hsa_circ_112565,RMVar_hsa_circ_161118,RMVar_hsa_circ_45216,RMVar_hsa_circ_161120,RMVar_hsa_circ_113421,RMVar_hsa_circ_161121,RMVar_hsa_circ_161122,RMVar_hsa_circ_342529 35366 RMVar_ID_35366 Human_SNP_ID_518694827 A-to-I Human chr12 + 122560606 122560564 122560607 TGTTGGCCAGACTAGTCTTGAACCCTGACTTCAAGTGATCTGCCTGCCTTGGCCTCCCAAAATGC __________________________________GTGATCTGCCTGCCTTGGCCTCCCAAAATGC GGTTTCACCATGTTGGCCAGACTAGTCTTGAACCCTGACTTCAA G KNTC1 Ensembl:ENSG00000184445 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1272039573 Functional Loss DEL dbSNP153 1..34 33 - - - RMVar_hsa_circ_107161,RMVar_hsa_circ_124960,RMVar_hsa_circ_161088,RMVar_hsa_circ_161091,RMVar_hsa_circ_378232,RMVar_hsa_circ_124033,RMVar_hsa_circ_81914,RMVar_hsa_circ_97580,RMVar_hsa_circ_5726,RMVar_hsa_circ_95867,RMVar_hsa_circ_161094,RMVar_hsa_circ_161095,RMVar_hsa_circ_161096,RMVar_hsa_circ_161093,RMVar_hsa_circ_161098,RMVar_hsa_circ_92703,RMVar_hsa_circ_161101,RMVar_hsa_circ_108321,RMVar_hsa_circ_111263,RMVar_hsa_circ_98991,RMVar_hsa_circ_161099,RMVar_hsa_circ_161100,RMVar_hsa_circ_112227,RMVar_hsa_circ_6652,RMVar_hsa_circ_161104,RMVar_hsa_circ_161105,RMVar_hsa_circ_50545,RMVar_hsa_circ_106319,RMVar_hsa_circ_71486,RMVar_hsa_circ_161108,RMVar_hsa_circ_161109,RMVar_hsa_circ_346904,RMVar_hsa_circ_376574,RMVar_hsa_circ_100924,RMVar_hsa_circ_49905,RMVar_hsa_circ_161113,RMVar_hsa_circ_96683,RMVar_hsa_circ_16878,RMVar_hsa_circ_161115,RMVar_hsa_circ_105638,RMVar_hsa_circ_320660,RMVar_hsa_circ_372340,RMVar_hsa_circ_161116,RMVar_hsa_circ_4115,RMVar_hsa_circ_161117,RMVar_hsa_circ_358681,RMVar_hsa_circ_25523,RMVar_hsa_circ_112565,RMVar_hsa_circ_161118,RMVar_hsa_circ_45216,RMVar_hsa_circ_161120,RMVar_hsa_circ_113421,RMVar_hsa_circ_161121,RMVar_hsa_circ_161122,RMVar_hsa_circ_342529 35367 RMVar_ID_35367 Human_SNP_ID_518694934 A-to-I Human chr12 + 122561054 122561054 122561054 GGATTCTTGGCTGGGTGCAGTGGCTCATGCCTATAATCCTAGCACTTTGGGAGGCCCAGGAGAGC GGATTCTTGGCTGGGTGCAGTGGCTCATGCCTGTAATCCTAGCACTTTGGGAGGCCCAGGAGAGC A G KNTC1 Ensembl:ENSG00000184445 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1423675158 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107161,RMVar_hsa_circ_124960,RMVar_hsa_circ_161088,RMVar_hsa_circ_161091,RMVar_hsa_circ_378232,RMVar_hsa_circ_124033,RMVar_hsa_circ_81914,RMVar_hsa_circ_97580,RMVar_hsa_circ_5726,RMVar_hsa_circ_95867,RMVar_hsa_circ_161094,RMVar_hsa_circ_161095,RMVar_hsa_circ_161096,RMVar_hsa_circ_161093,RMVar_hsa_circ_161098,RMVar_hsa_circ_92703,RMVar_hsa_circ_161101,RMVar_hsa_circ_108321,RMVar_hsa_circ_111263,RMVar_hsa_circ_98991,RMVar_hsa_circ_161099,RMVar_hsa_circ_161100,RMVar_hsa_circ_112227,RMVar_hsa_circ_6652,RMVar_hsa_circ_161104,RMVar_hsa_circ_161105,RMVar_hsa_circ_50545,RMVar_hsa_circ_106319,RMVar_hsa_circ_71486,RMVar_hsa_circ_161108,RMVar_hsa_circ_161109,RMVar_hsa_circ_346904,RMVar_hsa_circ_376574,RMVar_hsa_circ_100924,RMVar_hsa_circ_49905,RMVar_hsa_circ_161113,RMVar_hsa_circ_96683,RMVar_hsa_circ_16878,RMVar_hsa_circ_161115,RMVar_hsa_circ_105638,RMVar_hsa_circ_320660,RMVar_hsa_circ_372340,RMVar_hsa_circ_161116,RMVar_hsa_circ_4115,RMVar_hsa_circ_161117,RMVar_hsa_circ_358681,RMVar_hsa_circ_25523,RMVar_hsa_circ_112565,RMVar_hsa_circ_161118,RMVar_hsa_circ_45216,RMVar_hsa_circ_161120,RMVar_hsa_circ_113421,RMVar_hsa_circ_161121,RMVar_hsa_circ_161122,RMVar_hsa_circ_342529 35368 RMVar_ID_35368 Human_SNP_ID_518694966 A-to-I Human chr12 + 122561230 122561230 122561230 CCAGCTACTTGGAAGGCTGAGGCAGGAGAATTACTTGAACCCAGAAGGTGGAGGTTGCAGTGAGC CCAGCTACTTGGAAGGCTGAGGCAGGAGAATTTCTTGAACCCAGAAGGTGGAGGTTGCAGTGAGC A T KNTC1 Ensembl:ENSG00000184445 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs78280246 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107161,RMVar_hsa_circ_124960,RMVar_hsa_circ_161088,RMVar_hsa_circ_161091,RMVar_hsa_circ_378232,RMVar_hsa_circ_124033,RMVar_hsa_circ_81914,RMVar_hsa_circ_97580,RMVar_hsa_circ_5726,RMVar_hsa_circ_95867,RMVar_hsa_circ_161094,RMVar_hsa_circ_161095,RMVar_hsa_circ_161096,RMVar_hsa_circ_161093,RMVar_hsa_circ_161098,RMVar_hsa_circ_92703,RMVar_hsa_circ_161101,RMVar_hsa_circ_108321,RMVar_hsa_circ_111263,RMVar_hsa_circ_98991,RMVar_hsa_circ_161099,RMVar_hsa_circ_161100,RMVar_hsa_circ_112227,RMVar_hsa_circ_6652,RMVar_hsa_circ_161104,RMVar_hsa_circ_161105,RMVar_hsa_circ_50545,RMVar_hsa_circ_106319,RMVar_hsa_circ_71486,RMVar_hsa_circ_161108,RMVar_hsa_circ_161109,RMVar_hsa_circ_346904,RMVar_hsa_circ_376574,RMVar_hsa_circ_100924,RMVar_hsa_circ_49905,RMVar_hsa_circ_161113,RMVar_hsa_circ_96683,RMVar_hsa_circ_16878,RMVar_hsa_circ_161115,RMVar_hsa_circ_105638,RMVar_hsa_circ_320660,RMVar_hsa_circ_372340,RMVar_hsa_circ_161116,RMVar_hsa_circ_4115,RMVar_hsa_circ_161117,RMVar_hsa_circ_358681,RMVar_hsa_circ_25523,RMVar_hsa_circ_112565,RMVar_hsa_circ_161118,RMVar_hsa_circ_45216,RMVar_hsa_circ_161120,RMVar_hsa_circ_113421,RMVar_hsa_circ_161121,RMVar_hsa_circ_161122,RMVar_hsa_circ_342529 35369 RMVar_ID_35369 Human_SNP_ID_518697927 A-to-I Human chr12 + 122572256 122572256 122572256 CCTAGTAAAAATACAAAAAAAATTAGCCAGGCATGGTGGTGGGTGCCTGTAGTCCTAGCTATTTG CCTAGTAAAAATACAAAAAAAATTAGCCAGGCCTGGTGGTGGGTGCCTGTAGTCCTAGCTATTTG A C KNTC1 Ensembl:ENSG00000184445 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs895127536 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107161,RMVar_hsa_circ_161088,RMVar_hsa_circ_378232,RMVar_hsa_circ_97580,RMVar_hsa_circ_898,RMVar_hsa_circ_95867,RMVar_hsa_circ_161095,RMVar_hsa_circ_161096,RMVar_hsa_circ_161098,RMVar_hsa_circ_92703,RMVar_hsa_circ_161101,RMVar_hsa_circ_108321,RMVar_hsa_circ_111263,RMVar_hsa_circ_98991,RMVar_hsa_circ_161099,RMVar_hsa_circ_161100,RMVar_hsa_circ_112227,RMVar_hsa_circ_6652,RMVar_hsa_circ_161104,RMVar_hsa_circ_161105,RMVar_hsa_circ_50545,RMVar_hsa_circ_71486,RMVar_hsa_circ_346904,RMVar_hsa_circ_100924,RMVar_hsa_circ_49905,RMVar_hsa_circ_161113,RMVar_hsa_circ_96683,RMVar_hsa_circ_161115,RMVar_hsa_circ_105638,RMVar_hsa_circ_320660,RMVar_hsa_circ_161116,RMVar_hsa_circ_161122,RMVar_hsa_circ_79909,RMVar_hsa_circ_161126,RMVar_hsa_circ_10772,RMVar_hsa_circ_271551,RMVar_hsa_circ_370315,RMVar_hsa_circ_161124,RMVar_hsa_circ_325022,RMVar_hsa_circ_161127,RMVar_hsa_circ_321335,RMVar_hsa_circ_161125,RMVar_hsa_circ_373976,RMVar_hsa_circ_341134,RMVar_hsa_circ_94258,RMVar_hsa_circ_270602,RMVar_hsa_circ_39518,RMVar_hsa_circ_126126,RMVar_hsa_circ_161129,RMVar_hsa_circ_161130,RMVar_hsa_circ_161131,RMVar_hsa_circ_369486,RMVar_hsa_circ_161128,RMVar_hsa_circ_82234,RMVar_hsa_circ_161133,RMVar_hsa_circ_99178,RMVar_hsa_circ_161134,RMVar_hsa_circ_161132,RMVar_hsa_circ_161135 35370 RMVar_ID_35370 Human_SNP_ID_518697928 A-to-I Human chr12 + 122572256 122572256 122572256 CCTAGTAAAAATACAAAAAAAATTAGCCAGGCATGGTGGTGGGTGCCTGTAGTCCTAGCTATTTG CCTAGTAAAAATACAAAAAAAATTAGCCAGGCGTGGTGGTGGGTGCCTGTAGTCCTAGCTATTTG A G KNTC1 Ensembl:ENSG00000184445 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs895127536 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107161,RMVar_hsa_circ_161088,RMVar_hsa_circ_378232,RMVar_hsa_circ_97580,RMVar_hsa_circ_898,RMVar_hsa_circ_95867,RMVar_hsa_circ_161095,RMVar_hsa_circ_161096,RMVar_hsa_circ_161098,RMVar_hsa_circ_92703,RMVar_hsa_circ_161101,RMVar_hsa_circ_108321,RMVar_hsa_circ_111263,RMVar_hsa_circ_98991,RMVar_hsa_circ_161099,RMVar_hsa_circ_161100,RMVar_hsa_circ_112227,RMVar_hsa_circ_6652,RMVar_hsa_circ_161104,RMVar_hsa_circ_161105,RMVar_hsa_circ_50545,RMVar_hsa_circ_71486,RMVar_hsa_circ_346904,RMVar_hsa_circ_100924,RMVar_hsa_circ_49905,RMVar_hsa_circ_161113,RMVar_hsa_circ_96683,RMVar_hsa_circ_161115,RMVar_hsa_circ_105638,RMVar_hsa_circ_320660,RMVar_hsa_circ_161116,RMVar_hsa_circ_161122,RMVar_hsa_circ_79909,RMVar_hsa_circ_161126,RMVar_hsa_circ_10772,RMVar_hsa_circ_271551,RMVar_hsa_circ_370315,RMVar_hsa_circ_161124,RMVar_hsa_circ_325022,RMVar_hsa_circ_161127,RMVar_hsa_circ_321335,RMVar_hsa_circ_161125,RMVar_hsa_circ_373976,RMVar_hsa_circ_341134,RMVar_hsa_circ_94258,RMVar_hsa_circ_270602,RMVar_hsa_circ_39518,RMVar_hsa_circ_126126,RMVar_hsa_circ_161129,RMVar_hsa_circ_161130,RMVar_hsa_circ_161131,RMVar_hsa_circ_369486,RMVar_hsa_circ_161128,RMVar_hsa_circ_82234,RMVar_hsa_circ_161133,RMVar_hsa_circ_99178,RMVar_hsa_circ_161134,RMVar_hsa_circ_161132,RMVar_hsa_circ_161135 35371 RMVar_ID_35371 Human_SNP_ID_518698498 A-to-I Human chr12 + 122574511 122574511 122574511 TGAGATGGGTCTGGCTGTGTCGCCCAGGCTGGAATGCAGTGACATGATCATGGTTCACTGCAGCC TGAGATGGGTCTGGCTGTGTCGCCCAGGCTGGCATGCAGTGACATGATCATGGTTCACTGCAGCC A C KNTC1 Ensembl:ENSG00000184445 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs990054102 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107161,RMVar_hsa_circ_161088,RMVar_hsa_circ_378232,RMVar_hsa_circ_97580,RMVar_hsa_circ_898,RMVar_hsa_circ_95867,RMVar_hsa_circ_161095,RMVar_hsa_circ_161096,RMVar_hsa_circ_161098,RMVar_hsa_circ_92703,RMVar_hsa_circ_161101,RMVar_hsa_circ_108321,RMVar_hsa_circ_111263,RMVar_hsa_circ_98991,RMVar_hsa_circ_161099,RMVar_hsa_circ_161100,RMVar_hsa_circ_112227,RMVar_hsa_circ_6652,RMVar_hsa_circ_161104,RMVar_hsa_circ_161105,RMVar_hsa_circ_50545,RMVar_hsa_circ_71486,RMVar_hsa_circ_100924,RMVar_hsa_circ_49905,RMVar_hsa_circ_161113,RMVar_hsa_circ_161115,RMVar_hsa_circ_105638,RMVar_hsa_circ_79909,RMVar_hsa_circ_161126,RMVar_hsa_circ_10772,RMVar_hsa_circ_271551,RMVar_hsa_circ_370315,RMVar_hsa_circ_161124,RMVar_hsa_circ_161127,RMVar_hsa_circ_321335,RMVar_hsa_circ_373976,RMVar_hsa_circ_341134,RMVar_hsa_circ_94258,RMVar_hsa_circ_39518,RMVar_hsa_circ_30260,RMVar_hsa_circ_126126,RMVar_hsa_circ_161129,RMVar_hsa_circ_161130,RMVar_hsa_circ_161131,RMVar_hsa_circ_161133,RMVar_hsa_circ_99178,RMVar_hsa_circ_161132,RMVar_hsa_circ_105211,RMVar_hsa_circ_127627,RMVar_hsa_circ_161136,RMVar_hsa_circ_14209,RMVar_hsa_circ_161138,RMVar_hsa_circ_16044,RMVar_hsa_circ_161137 35372 RMVar_ID_35372 Human_SNP_ID_518698522 A-to-I Human chr12 + 122574614 122574614 122574614 CTGAGTAGTTAGGACCATAGGCGTGTGCCACTACGCCCAGCTAATTTTTGTATTTTTTGTAGAGA CTGAGTAGTTAGGACCATAGGCGTGTGCCACTTCGCCCAGCTAATTTTTGTATTTTTTGTAGAGA A T KNTC1 Ensembl:ENSG00000184445 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1044541093 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107161,RMVar_hsa_circ_161088,RMVar_hsa_circ_378232,RMVar_hsa_circ_97580,RMVar_hsa_circ_898,RMVar_hsa_circ_95867,RMVar_hsa_circ_161095,RMVar_hsa_circ_161096,RMVar_hsa_circ_161098,RMVar_hsa_circ_92703,RMVar_hsa_circ_161101,RMVar_hsa_circ_108321,RMVar_hsa_circ_111263,RMVar_hsa_circ_98991,RMVar_hsa_circ_161099,RMVar_hsa_circ_161100,RMVar_hsa_circ_112227,RMVar_hsa_circ_6652,RMVar_hsa_circ_161104,RMVar_hsa_circ_161105,RMVar_hsa_circ_50545,RMVar_hsa_circ_71486,RMVar_hsa_circ_100924,RMVar_hsa_circ_49905,RMVar_hsa_circ_161113,RMVar_hsa_circ_161115,RMVar_hsa_circ_105638,RMVar_hsa_circ_79909,RMVar_hsa_circ_161126,RMVar_hsa_circ_10772,RMVar_hsa_circ_271551,RMVar_hsa_circ_370315,RMVar_hsa_circ_161124,RMVar_hsa_circ_161127,RMVar_hsa_circ_321335,RMVar_hsa_circ_373976,RMVar_hsa_circ_341134,RMVar_hsa_circ_94258,RMVar_hsa_circ_39518,RMVar_hsa_circ_30260,RMVar_hsa_circ_126126,RMVar_hsa_circ_161129,RMVar_hsa_circ_161130,RMVar_hsa_circ_161131,RMVar_hsa_circ_161133,RMVar_hsa_circ_99178,RMVar_hsa_circ_161132,RMVar_hsa_circ_105211,RMVar_hsa_circ_127627,RMVar_hsa_circ_161136,RMVar_hsa_circ_14209,RMVar_hsa_circ_161138,RMVar_hsa_circ_16044,RMVar_hsa_circ_161137 35373 RMVar_ID_35373 Human_SNP_ID_518699047 A-to-I Human chr12 + 122576622 122576622 122576622 AGAATCACTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCCGAGATTGCGCCACTGCACTGTAGCC AGAATCACTTGAACCTGGGAGGCAGAGGTTGCGGTGAGCCGAGATTGCGCCACTGCACTGTAGCC A G KNTC1 Ensembl:ENSG00000184445 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs369012685 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23306235 RMVar_hsa_circ_107161,RMVar_hsa_circ_161088,RMVar_hsa_circ_378232,RMVar_hsa_circ_97580,RMVar_hsa_circ_898,RMVar_hsa_circ_95867,RMVar_hsa_circ_161095,RMVar_hsa_circ_161096,RMVar_hsa_circ_161098,RMVar_hsa_circ_92703,RMVar_hsa_circ_161101,RMVar_hsa_circ_108321,RMVar_hsa_circ_111263,RMVar_hsa_circ_98991,RMVar_hsa_circ_161099,RMVar_hsa_circ_161100,RMVar_hsa_circ_112227,RMVar_hsa_circ_6652,RMVar_hsa_circ_161104,RMVar_hsa_circ_161105,RMVar_hsa_circ_50545,RMVar_hsa_circ_71486,RMVar_hsa_circ_100924,RMVar_hsa_circ_49905,RMVar_hsa_circ_161113,RMVar_hsa_circ_161115,RMVar_hsa_circ_105638,RMVar_hsa_circ_79909,RMVar_hsa_circ_161126,RMVar_hsa_circ_10772,RMVar_hsa_circ_271551,RMVar_hsa_circ_370315,RMVar_hsa_circ_161124,RMVar_hsa_circ_161127,RMVar_hsa_circ_321335,RMVar_hsa_circ_373976,RMVar_hsa_circ_341134,RMVar_hsa_circ_94258,RMVar_hsa_circ_39518,RMVar_hsa_circ_30260,RMVar_hsa_circ_161129,RMVar_hsa_circ_161130,RMVar_hsa_circ_161131,RMVar_hsa_circ_99178,RMVar_hsa_circ_161132,RMVar_hsa_circ_105211,RMVar_hsa_circ_127627,RMVar_hsa_circ_161136,RMVar_hsa_circ_8872,RMVar_hsa_circ_346366,RMVar_hsa_circ_14209,RMVar_hsa_circ_161138,RMVar_hsa_circ_16044,RMVar_hsa_circ_161137,RMVar_hsa_circ_371228,RMVar_hsa_circ_375437,RMVar_hsa_circ_348774,RMVar_hsa_circ_123469,RMVar_hsa_circ_70301,RMVar_hsa_circ_87561,RMVar_hsa_circ_161140,RMVar_hsa_circ_161141,RMVar_hsa_circ_161142,RMVar_hsa_circ_161139,RMVar_hsa_circ_367545,RMVar_hsa_circ_161143 35374 RMVar_ID_35374 Human_SNP_ID_518704224 A-to-I Human chr12 + 122596283 122596283 122596283 TATTTGTATTTTAGTAGAGACCGGGTTTCACCATGTTACCTAGGCTGGTCTTGAACTCCTGAGCT TATTTGTATTTTAGTAGAGACCGGGTTTCACCGTGTTACCTAGGCTGGTCTTGAACTCCTGAGCT A G KNTC1 Ensembl:ENSG00000184445 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1407885482 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11858311 RMVar_hsa_circ_97580,RMVar_hsa_circ_7551,RMVar_hsa_circ_161096,RMVar_hsa_circ_112227,RMVar_hsa_circ_161105,RMVar_hsa_circ_100924,RMVar_hsa_circ_161113,RMVar_hsa_circ_105211,RMVar_hsa_circ_161136,RMVar_hsa_circ_14209,RMVar_hsa_circ_109604,RMVar_hsa_circ_358718,RMVar_hsa_circ_100128,RMVar_hsa_circ_161144,RMVar_hsa_circ_161146,RMVar_hsa_circ_161145,RMVar_hsa_circ_125175,RMVar_hsa_circ_161155,RMVar_hsa_circ_43314,RMVar_hsa_circ_161159,RMVar_hsa_circ_29509,RMVar_hsa_circ_61870,RMVar_hsa_circ_364994,RMVar_hsa_circ_370524,RMVar_hsa_circ_327299,RMVar_hsa_circ_17609,RMVar_hsa_circ_76670,RMVar_hsa_circ_113587,RMVar_hsa_circ_20242,RMVar_hsa_circ_13541,RMVar_hsa_circ_161160,RMVar_hsa_circ_25254,RMVar_hsa_circ_161158,RMVar_hsa_circ_303143,RMVar_hsa_circ_333375,RMVar_hsa_circ_301722,RMVar_hsa_circ_161169,RMVar_hsa_circ_161170,RMVar_hsa_circ_161171,RMVar_hsa_circ_161168 35375 RMVar_ID_35375 Human_SNP_ID_518704234 A-to-I Human chr12 + 122596317 122596317 122596317 GTTACCTAGGCTGGTCTTGAACTCCTGAGCTCAGGCAATCCACCCGTCTCGACCTCCCAAAGTGC GTTACCTAGGCTGGTCTTGAACTCCTGAGCTCGGGCAATCCACCCGTCTCGACCTCCCAAAGTGC A G KNTC1 Ensembl:ENSG00000184445 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs926032651 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11858311 RMVar_hsa_circ_97580,RMVar_hsa_circ_7551,RMVar_hsa_circ_161096,RMVar_hsa_circ_112227,RMVar_hsa_circ_161105,RMVar_hsa_circ_100924,RMVar_hsa_circ_161113,RMVar_hsa_circ_105211,RMVar_hsa_circ_161136,RMVar_hsa_circ_14209,RMVar_hsa_circ_109604,RMVar_hsa_circ_358718,RMVar_hsa_circ_100128,RMVar_hsa_circ_161144,RMVar_hsa_circ_161146,RMVar_hsa_circ_161145,RMVar_hsa_circ_125175,RMVar_hsa_circ_161155,RMVar_hsa_circ_43314,RMVar_hsa_circ_161159,RMVar_hsa_circ_29509,RMVar_hsa_circ_61870,RMVar_hsa_circ_364994,RMVar_hsa_circ_370524,RMVar_hsa_circ_327299,RMVar_hsa_circ_17609,RMVar_hsa_circ_76670,RMVar_hsa_circ_113587,RMVar_hsa_circ_20242,RMVar_hsa_circ_13541,RMVar_hsa_circ_161160,RMVar_hsa_circ_25254,RMVar_hsa_circ_161158,RMVar_hsa_circ_303143,RMVar_hsa_circ_333375,RMVar_hsa_circ_301722,RMVar_hsa_circ_161169,RMVar_hsa_circ_161170,RMVar_hsa_circ_161171,RMVar_hsa_circ_161168 35376 RMVar_ID_35376 Human_SNP_ID_518704235 A-to-I Human chr12 + 122596321 122596321 122596321 CCTAGGCTGGTCTTGAACTCCTGAGCTCAGGCAATCCACCCGTCTCGACCTCCCAAAGTGCTAGG CCTAGGCTGGTCTTGAACTCCTGAGCTCAGGCGATCCACCCGTCTCGACCTCCCAAAGTGCTAGG A G KNTC1 Ensembl:ENSG00000184445 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs933558030 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11858312 RMVar_hsa_circ_97580,RMVar_hsa_circ_7551,RMVar_hsa_circ_161096,RMVar_hsa_circ_112227,RMVar_hsa_circ_161105,RMVar_hsa_circ_100924,RMVar_hsa_circ_161113,RMVar_hsa_circ_105211,RMVar_hsa_circ_161136,RMVar_hsa_circ_14209,RMVar_hsa_circ_109604,RMVar_hsa_circ_358718,RMVar_hsa_circ_100128,RMVar_hsa_circ_161144,RMVar_hsa_circ_161146,RMVar_hsa_circ_161145,RMVar_hsa_circ_125175,RMVar_hsa_circ_161155,RMVar_hsa_circ_43314,RMVar_hsa_circ_161159,RMVar_hsa_circ_29509,RMVar_hsa_circ_61870,RMVar_hsa_circ_364994,RMVar_hsa_circ_370524,RMVar_hsa_circ_327299,RMVar_hsa_circ_17609,RMVar_hsa_circ_76670,RMVar_hsa_circ_113587,RMVar_hsa_circ_20242,RMVar_hsa_circ_13541,RMVar_hsa_circ_161160,RMVar_hsa_circ_25254,RMVar_hsa_circ_161158,RMVar_hsa_circ_303143,RMVar_hsa_circ_333375,RMVar_hsa_circ_301722,RMVar_hsa_circ_161169,RMVar_hsa_circ_161170,RMVar_hsa_circ_161171,RMVar_hsa_circ_161168 35377 RMVar_ID_35377 Human_SNP_ID_518704882 A-to-I Human chr12 + 122598498 122598498 122598498 GCTGGAGTGCAGTGGTATGAATGTGACTCACTACAGCCTCTATGTCCTGGGCTCAAGTGATACTC GCTGGAGTGCAGTGGTATGAATGTGACTCACTGCAGCCTCTATGTCCTGGGCTCAAGTGATACTC A G KNTC1 Ensembl:ENSG00000184445 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893514447 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11858403 RMVar_hsa_circ_97580,RMVar_hsa_circ_7551,RMVar_hsa_circ_161096,RMVar_hsa_circ_100924,RMVar_hsa_circ_161113,RMVar_hsa_circ_105211,RMVar_hsa_circ_161136,RMVar_hsa_circ_14209,RMVar_hsa_circ_109604,RMVar_hsa_circ_358718,RMVar_hsa_circ_100128,RMVar_hsa_circ_161144,RMVar_hsa_circ_161146,RMVar_hsa_circ_161145,RMVar_hsa_circ_125175,RMVar_hsa_circ_161155,RMVar_hsa_circ_43314,RMVar_hsa_circ_161159,RMVar_hsa_circ_29509,RMVar_hsa_circ_61870,RMVar_hsa_circ_364994,RMVar_hsa_circ_327299,RMVar_hsa_circ_17609,RMVar_hsa_circ_76670,RMVar_hsa_circ_113587,RMVar_hsa_circ_20242,RMVar_hsa_circ_13541,RMVar_hsa_circ_25254,RMVar_hsa_circ_161158,RMVar_hsa_circ_303143,RMVar_hsa_circ_333375,RMVar_hsa_circ_301722,RMVar_hsa_circ_74174,RMVar_hsa_circ_161169,RMVar_hsa_circ_161170,RMVar_hsa_circ_161171,RMVar_hsa_circ_161168,RMVar_hsa_circ_265556,RMVar_hsa_circ_309209,RMVar_hsa_circ_161172 35378 RMVar_ID_35378 Human_SNP_ID_518712544 A-to-I Human chr12 + 122627497 122627497 122627497 CTCCTGCTTCAGCCTCCCGAGTATCTGGGACTACAGGCACACACCACCATGCTTTCCTGATTTTT CTCCTGCTTCAGCCTCCCGAGTATCTGGGACTGCAGGCACACACCACCATGCTTTCCTGATTTTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs868608709 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_161168 35379 RMVar_ID_35379 Human_SNP_ID_518721204 A-to-I Human chr12 + 122662080 122662080 122662080 TATTTATTCATTTATTATAGAAATGGGGTCTTACTATGTTGCCCAGTCTGATCTTGAACTCCTGG TATTTATTCATTTATTATAGAAATGGGGTCTTGCTATGTTGCCCAGTCTGATCTTGAACTCCTGG A G lnc-KNTC1-3 RNACentral:URS00008B6387 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1021987014 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_161168 35380 RMVar_ID_35380 Human_SNP_ID_518747421 A-to-I Human chr12 + 122758127 122758127 122758127 GGAGTCTCACTCTGTTGCCCAGACTGGAGTGTAATGGCGTGATCTCGGCTCACTGCAACCTCCGC GGAGTCTCACTCTGTTGCCCAGACTGGAGTGTGATGGCGTGATCTCGGCTCACTGCAACCTCCGC A G DENR Ensembl:ENSG00000139726 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs915157918 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6146820 RMVar_hsa_circ_70314,RMVar_hsa_circ_62754 35381 RMVar_ID_35381 Human_SNP_ID_518747435 A-to-I Human chr12 + 122758171 122758171 122758171 TCGGCTCACTGCAACCTCCGCCTCCAGGGTTCAAGTGATTCTCCTGGTTCAGCCTCCCGAGTAGC TCGGCTCACTGCAACCTCCGCCTCCAGGGTTCTAGTGATTCTCCTGGTTCAGCCTCCCGAGTAGC A T DENR Ensembl:ENSG00000139726 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs994333490 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70314,RMVar_hsa_circ_62754 35382 RMVar_ID_35382 Human_SNP_ID_518747449 A-to-I Human chr12 + 122758211 122758211 122758211 CTCCTGGTTCAGCCTCCCGAGTAGCGGAGATTACAGGCGCCTGCCACCGTGCCTGGCTGATTTTT CTCCTGGTTCAGCCTCCCGAGTAGCGGAGATTCCAGGCGCCTGCCACCGTGCCTGGCTGATTTTT A C DENR Ensembl:ENSG00000139726 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1245338495 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70314,RMVar_hsa_circ_62754 35383 RMVar_ID_35383 Human_SNP_ID_518747567 A-to-I Human chr12 + 122758759 122758759 122758759 CCCAGGAGTTCAAGGCTGCATGAGTTAAGATCACATCACTGCACTATAGCCTGGGTGACAAAGTG CCCAGGAGTTCAAGGCTGCATGAGTTAAGATCGCATCACTGCACTATAGCCTGGGTGACAAAGTG A G DENR Ensembl:ENSG00000139726 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1317453922 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11859935 RMVar_hsa_circ_70314,RMVar_hsa_circ_62754 35384 RMVar_ID_35384 Human_SNP_ID_518747570 A-to-I Human chr12 + 122758772 122758772 122758772 GGCTGCATGAGTTAAGATCACATCACTGCACTATAGCCTGGGTGACAAAGTGAGACTGTCTCTTT GGCTGCATGAGTTAAGATCACATCACTGCACTGTAGCCTGGGTGACAAAGTGAGACTGTCTCTTT A G DENR Ensembl:ENSG00000139726 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941516439 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11859935 RMVar_hsa_circ_70314,RMVar_hsa_circ_62754 35385 RMVar_ID_35385 Human_SNP_ID_518747750 A-to-I Human chr12 + 122759437 122759437 122759437 TTTATTGCATTAGAATTTTGCTGAACCGGGCCAGGCACAGTGGCTCACACCTGTAATCACAGCAC TTTATTGCATTAGAATTTTGCTGAACCGGGCCGGGCACAGTGGCTCACACCTGTAATCACAGCAC A G DENR Ensembl:ENSG00000139726 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs568240359 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_754888,Human_RBP_ID_6146831,Human_RBP_ID_11859956 RMVar_hsa_circ_70314,RMVar_hsa_circ_62754 35386 RMVar_ID_35386 Human_SNP_ID_518747753 A-to-I Human chr12 + 122759443 122759443 122759443 GCATTAGAATTTTGCTGAACCGGGCCAGGCACAGTGGCTCACACCTGTAATCACAGCACTTTGGG GCATTAGAATTTTGCTGAACCGGGCCAGGCACGGTGGCTCACACCTGTAATCACAGCACTTTGGG A G DENR Ensembl:ENSG00000139726 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs921457045 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_754888,Human_RBP_ID_6146831,Human_RBP_ID_11859956 RMVar_hsa_circ_70314,RMVar_hsa_circ_62754 35387 RMVar_ID_35387 Human_SNP_ID_518747788 A-to-I Human chr12 + 122759636 122759636 122759636 CCAGCTACTCGGGAGGCTGAGCTACGAGAATCACTTGGACCCAGGAGGTAGAGGTTGCAGCCAGC CCAGCTACTCGGGAGGCTGAGCTACGAGAATCGCTTGGACCCAGGAGGTAGAGGTTGCAGCCAGC A G DENR Ensembl:ENSG00000139726 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1481844568 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6146834,Human_RBP_ID_11859963 RMVar_hsa_circ_70314,RMVar_hsa_circ_62754 35388 RMVar_ID_35388 Human_SNP_ID_518747792 A-to-I Human chr12 + 122759646 122759646 122759646 GGGAGGCTGAGCTACGAGAATCACTTGGACCCAGGAGGTAGAGGTTGCAGCCAGCTGAGATGGTG GGGAGGCTGAGCTACGAGAATCACTTGGACCCCGGAGGTAGAGGTTGCAGCCAGCTGAGATGGTG A C DENR Ensembl:ENSG00000139726 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941147564 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6146834,Human_RBP_ID_11859964 RMVar_hsa_circ_70314,RMVar_hsa_circ_62754 35389 RMVar_ID_35389 Human_SNP_ID_518747793 A-to-I Human chr12 + 122759646 122759646 122759646 GGGAGGCTGAGCTACGAGAATCACTTGGACCCAGGAGGTAGAGGTTGCAGCCAGCTGAGATGGTG GGGAGGCTGAGCTACGAGAATCACTTGGACCCGGGAGGTAGAGGTTGCAGCCAGCTGAGATGGTG A G DENR Ensembl:ENSG00000139726 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941147564 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6146834,Human_RBP_ID_11859964 RMVar_hsa_circ_70314,RMVar_hsa_circ_62754 35390 RMVar_ID_35390 Human_SNP_ID_518747801 A-to-I Human chr12 + 122759666 122759666 122759666 TCACTTGGACCCAGGAGGTAGAGGTTGCAGCCAGCTGAGATGGTGCCATTGCACTCCAGCCTGGG TCACTTGGACCCAGGAGGTAGAGGTTGCAGCCCGCTGAGATGGTGCCATTGCACTCCAGCCTGGG A C DENR Ensembl:ENSG00000139726 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1300006437 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6146834,Human_RBP_ID_11859964 RMVar_hsa_circ_70314,RMVar_hsa_circ_62754 35391 RMVar_ID_35391 Human_SNP_ID_518747802 A-to-I Human chr12 + 122759666 122759666 122759666 TCACTTGGACCCAGGAGGTAGAGGTTGCAGCCAGCTGAGATGGTGCCATTGCACTCCAGCCTGGG TCACTTGGACCCAGGAGGTAGAGGTTGCAGCCGGCTGAGATGGTGCCATTGCACTCCAGCCTGGG A G DENR Ensembl:ENSG00000139726 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1300006437 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6146834,Human_RBP_ID_11859964 RMVar_hsa_circ_70314,RMVar_hsa_circ_62754 35392 RMVar_ID_35392 Human_SNP_ID_518750138 A-to-I Human chr12 + 122769156 122769151 122769157 ATGGCCAAAGGGAGAGAGGCCTTTTAAAATATATATATATATACACATATATATGTATATATACA ATGGCCAAAGGGAGAGAGGCCTTTTAAA______ATATATATACACATATATATGTATATATACA AATATAT A DENR Ensembl:ENSG00000139726 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs886558609 Functional Loss DEL dbSNP153 29..34 33 - - - Human_RBP_ID_26413215 35393 RMVar_ID_35393 Human_SNP_ID_518750139 A-to-I Human chr12 + 122769156 122769151 122769157 ATGGCCAAAGGGAGAGAGGCCTTTTAAAATATATATATATATACACATATATATGTATATATACA ATGGCCAAAGGGAGAGAGGCCTTTTAAAATAT__ATATATATACACATATATATGTATATATACA AATATAT AATAT DENR Ensembl:ENSG00000139726 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs886558609 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_26413215 35394 RMVar_ID_35394 Human_SNP_ID_518750146 A-to-I Human chr12 + 122769158 122769158 122769158 GGCCAAAGGGAGAGAGGCCTTTTAAAATATATATATATATACACATATATATGTATATATACACA GGCCAAAGGGAGAGAGGCCTTTTAAAATATATGTATATATACACATATATATGTATATATACACA A G DENR Ensembl:ENSG00000139726 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1213131252 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26413215 35395 RMVar_ID_35395 Human_SNP_ID_518750153 A-to-I Human chr12 + 122769164 122769164 122769164 AGGGAGAGAGGCCTTTTAAAATATATATATATATACACATATATATGTATATATACACATATATG AGGGAGAGAGGCCTTTTAAAATATATATATATGTACACATATATATGTATATATACACATATATG A G DENR Ensembl:ENSG00000139726 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1045743 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26413215 35396 RMVar_ID_35396 Human_SNP_ID_518750155 A-to-I Human chr12 + 122769166 122769165 122769167 GGAGAGAGGCCTTTTAAAATATATATATATATACACATATATATGTATATATACACATATATGTA GGAGAGAGGCCTTTTAAAATATATATATATAT__ACATATATATGTATATATACACATATATGTA TAC T DENR Ensembl:ENSG00000139726 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1034623576 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_26413215 35397 RMVar_ID_35397 Human_SNP_ID_518750234 A-to-I Human chr12 + 122769242 122769242 122769242 ATACACATGTATATATACATGTGTGTATGTATACATGTATATATATATACATACACATATATGTA ATACACATGTATATATACATGTGTGTATGTATGCATGTATATATATATACATACACATATATGTA A G DENR Ensembl:ENSG00000139726 Protein coding intron GSE47997;GSE38233;GSE38233 K562 cells&HepG2 cells;cultured B-cells;cultured B-cells - 23474544,24183664,24183664 RNA-Seq:(High) rs1198111088 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3396731,Human_RBP_ID_18620583,Human_RBP_ID_26413221 35398 RMVar_ID_35398 Human_SNP_ID_518750668 A-to-I Human chr12 - 122770272 122770272 122770272 CCATCACTTCTTTAACCATTTCCCAATTGTTCATTTATAACATTTGCAATTTTTTATTATAAATA CCATCACTTCTTTAACCATTTCCCAATTGTTCTTTTATAACATTTGCAATTTTTTATTATAAATA T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs564486590 Functional Loss SNV dbSNP153 33..33 33 - - - 35399 RMVar_ID_35399 Human_SNP_ID_518750669 A-to-I Human chr12 - 122770272 122770272 122770272 CCATCACTTCTTTAACCATTTCCCAATTGTTCATTTATAACATTTGCAATTTTTTATTATAAATA CCATCACTTCTTTAACCATTTCCCAATTGTTCGTTTATAACATTTGCAATTTTTTATTATAAATA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs564486590 Functional Loss SNV dbSNP153 33..33 33 - - - 35400 RMVar_ID_35400 Human_SNP_ID_518751276 A-to-I Human chr12 + 122772755 122772755 122772755 TTTTTTTTTTTTTTGATACGGAGTGTCCCTCTATTGCCTAGGCTGGAGTGAGGTGGCGCAGTCTT TTTTTTTTTTTTTTGATACGGAGTGTCCCTCTGTTGCCTAGGCTGGAGTGAGGTGGCGCAGTCTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1384204772 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6146983,Human_RBP_ID_11860353 RMVar_hsa_circ_161179 35401 RMVar_ID_35401 Human_SNP_ID_518751308 A-to-I Human chr12 + 122772858 122772858 122772858 CTCCTGCCTCAGCCTTCCGAGTAGCTGGGACTATGGGTGCGCACCACCACACGTGGCTAGTTTTT CTCCTGCCTCAGCCTTCCGAGTAGCTGGGACTGTGGGTGCGCACCACCACACGTGGCTAGTTTTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1039315757 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6146985 RMVar_hsa_circ_161179 35402 RMVar_ID_35402 Human_SNP_ID_518751541 A-to-I Human chr12 + 122773570 122773570 122773570 GTCTCAAACTCCTGAACGCAACAGATCCTCCTACATTGGCCTCCCAAAGTGCTGGGGTTACAGGC GTCTCAAACTCCTGAACGCAACAGATCCTCCTCCATTGGCCTCCCAAAGTGCTGGGGTTACAGGC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910771296 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11860366 RMVar_hsa_circ_161179 35403 RMVar_ID_35403 Human_SNP_ID_518751542 A-to-I Human chr12 + 122773570 122773570 122773570 GTCTCAAACTCCTGAACGCAACAGATCCTCCTACATTGGCCTCCCAAAGTGCTGGGGTTACAGGC GTCTCAAACTCCTGAACGCAACAGATCCTCCTGCATTGGCCTCCCAAAGTGCTGGGGTTACAGGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910771296 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11860366 RMVar_hsa_circ_161179 35404 RMVar_ID_35404 Human_SNP_ID_518762365 A-to-I Human chr12 + 122815028 122815028 122815028 CTGTTTGCCAGGCTGCTTGAACTCCCGGCCTCAAGTAATCCTCCTGCCTCAGCCTCCCAAAGTGT CTGTTTGCCAGGCTGCTTGAACTCCCGGCCTCGAGTAATCCTCCTGCCTCAGCCTCCCAAAGTGT A G CCDC62 Ensembl:ENSG00000130783 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1159818371 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_328157,RMVar_hsa_circ_310972,RMVar_hsa_circ_161195 35405 RMVar_ID_35405 Human_SNP_ID_518778874 A-to-I Human chr12 - 122869718 122869718 122869718 GTGAAATAAGCTGGGGGTGGTGGTGCTCGCCTATAGTCCCACCTACTCTGAAGGCTGAGGCCACA GTGAAATAAGCTGGGGGTGGTGGTGCTCGCCTGTAGTCCCACCTACTCTGAAGGCTGAGGCCACA T C VPS37B Ensembl:ENSG00000139722 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs556991695 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37382 35406 RMVar_ID_35406 Human_SNP_ID_518779070 A-to-I Human chr12 - 122870569 122870569 122870569 ACCCCAAGCAGGCTAGTTTTTCATTTTTTTGCAGAGAGGTTGTCTTGCTATGTTGCCCAGGCTGG ACCCCAAGCAGGCTAGTTTTTCATTTTTTTGCGGAGAGGTTGTCTTGCTATGTTGCCCAGGCTGG T C AC027290.3,VPS37B Ensembl:ENSG00000280138,Ensembl:ENSG00000139722 Other,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1024637364 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37382 35407 RMVar_ID_35407 Human_SNP_ID_518782961 A-to-I Human chr12 - 122886408 122886408 122886408 CTATGGTTTCCTAGGCTGTTCTCAAACTCCTGAGCTCAAGCAATCCTTCTGCCTTGGCCTCTCGA CTATGGTTTCCTAGGCTGTTCTCAAACTCCTGGGCTCAAGCAATCCTTCTGCCTTGGCCTCTCGA T C AC027290.3,VPS37B Ensembl:ENSG00000280138,Ensembl:ENSG00000139722 Other,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1199112498 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3421971 35408 RMVar_ID_35408 Human_SNP_ID_518801138 A-to-I Human chr12 - 122959269 122959269 122959269 CAGGTCACTGCAACCTCTGCCTCCCAGCTTCAAGTGATTCTCCTGCCTCAGCCTCTCAAGTAGCT CAGGTCACTGCAACCTCTGCCTCCCAGCTTCAGGTGATTCTCCTGCCTCAGCCTCTCAAGTAGCT T C ABCB9 Ensembl:ENSG00000150967 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031090361 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104417,RMVar_hsa_circ_161221 35409 RMVar_ID_35409 Human_SNP_ID_518808554 A-to-I Human chr12 - 122983729 122983729 122983729 CGCCCCACCACCTGCCTTCTCTTTGATTTCTAAAGAGGGATTCAGCAGAGACCCCCCACCCCTCC CGCCCCACCACCTGCCTTCTCTTTGATTTCTAGAGAGGGATTCAGCAGAGACCCCCCACCCCTCC T C PITPNM2 Ensembl:ENSG00000090975 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1054921067 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118403,RMVar_hsa_circ_161227 35410 RMVar_ID_35410 Human_SNP_ID_518848632 A-to-I Human chr12 - 123157760 123157760 123157760 AAATGAGGCTGGGTATAGTGGCTTATGCCTATAATCCCAGCACTTTGGGAGGCCGAGGTGGGTGG AAATGAGGCTGGGTATAGTGGCTTATGCCTATGATCCCAGCACTTTGGGAGGCCGAGGTGGGTGG T C MPHOSPH9 Ensembl:ENSG00000051825 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1257425044 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81544,RMVar_hsa_circ_98333,RMVar_hsa_circ_161237,RMVar_hsa_circ_161238 35411 RMVar_ID_35411 Human_SNP_ID_518848633 A-to-I Human chr12 - 123157762 123157762 123157762 TAAAATGAGGCTGGGTATAGTGGCTTATGCCTATAATCCCAGCACTTTGGGAGGCCGAGGTGGGT TAAAATGAGGCTGGGTATAGTGGCTTATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGT T C MPHOSPH9 Ensembl:ENSG00000051825 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs373842917 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24944011 RMVar_hsa_circ_81544,RMVar_hsa_circ_98333,RMVar_hsa_circ_161237,RMVar_hsa_circ_161238 35412 RMVar_ID_35412 Human_SNP_ID_518848760 A-to-I Human chr12 - 123158221 123158221 123158221 GGAGGCTGAGGTGGGCAGATCAGATCACCTGCAGTCAGGAGTTCAAGACCAGCTTGGCCAATATG GGAGGCTGAGGTGGGCAGATCAGATCACCTGCGGTCAGGAGTTCAAGACCAGCTTGGCCAATATG T C MPHOSPH9 Ensembl:ENSG00000051825 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048167500 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81544,RMVar_hsa_circ_98333,RMVar_hsa_circ_161237,RMVar_hsa_circ_161238 35413 RMVar_ID_35413 Human_SNP_ID_518848761 A-to-I Human chr12 - 123158221 123158221 123158221 GGAGGCTGAGGTGGGCAGATCAGATCACCTGCAGTCAGGAGTTCAAGACCAGCTTGGCCAATATG GGAGGCTGAGGTGGGCAGATCAGATCACCTGCCGTCAGGAGTTCAAGACCAGCTTGGCCAATATG T G MPHOSPH9 Ensembl:ENSG00000051825 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048167500 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81544,RMVar_hsa_circ_98333,RMVar_hsa_circ_161237,RMVar_hsa_circ_161238 35414 RMVar_ID_35414 Human_SNP_ID_518848858 A-to-I Human chr12 - 123158665 123158663 123158665 ATTGCACCACTGCACTCCAGTCAGGGCAACAGAGTGAGACTGTGTCTCAAAAAAAAAAAAATTGA ATTGCACCACTGCACTCCAGTCAGGGCAACAG__TGAGACTGTGTCTCAAAAAAAAAAAAATTGA ACT A MPHOSPH9 Ensembl:ENSG00000051825 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335898329 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_81544,RMVar_hsa_circ_98333,RMVar_hsa_circ_161237,RMVar_hsa_circ_161238 35415 RMVar_ID_35415 Human_SNP_ID_518848861 A-to-I Human chr12 - 123158692 123158692 123158692 AAGAGTTGGAGGTTGCAGTGAGCTGAGATTGCACCACTGCACTCCAGTCAGGGCAACAGAGTGAG AAGAGTTGGAGGTTGCAGTGAGCTGAGATTGCGCCACTGCACTCCAGTCAGGGCAACAGAGTGAG T C MPHOSPH9 Ensembl:ENSG00000051825 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs930528113 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9668838,Human_RBP_ID_25020403 RMVar_hsa_circ_81544,RMVar_hsa_circ_98333,RMVar_hsa_circ_161237,RMVar_hsa_circ_161238 35416 RMVar_ID_35416 Human_SNP_ID_518848879 A-to-I Human chr12 - 123158768 123158768 123158768 AAAAATTAGCCGGTTGTGGTGGTGTGCCTGCAATCTCAGCTACTTGGAGGCTGAGGCAGGAGGTT AAAAATTAGCCGGTTGTGGTGGTGTGCCTGCAGTCTCAGCTACTTGGAGGCTGAGGCAGGAGGTT T C MPHOSPH9 Ensembl:ENSG00000051825 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs185813279 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81544,RMVar_hsa_circ_98333,RMVar_hsa_circ_161237,RMVar_hsa_circ_161238 35417 RMVar_ID_35417 Human_SNP_ID_518848903 A-to-I Human chr12 - 123158873 123158873 123158873 TAATCTCAGCACTTTGGGAGGCCAAGGTGGGCAGATCACTTGAGGTCAGGAGTTTGAGGCCGGCC TAATCTCAGCACTTTGGGAGGCCAAGGTGGGCGGATCACTTGAGGTCAGGAGTTTGAGGCCGGCC T C MPHOSPH9 Ensembl:ENSG00000051825 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2695481 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81544,RMVar_hsa_circ_98333,RMVar_hsa_circ_161237,RMVar_hsa_circ_161238 35418 RMVar_ID_35418 Human_SNP_ID_518848940 A-to-I Human chr12 - 123159044 123159044 123159044 GCTGTGTCACCAGGCTGGAGCGCAGTGACGCAATCTCGGCTCACTGCAGCCTCCAACTCCCTGGT GCTGTGTCACCAGGCTGGAGCGCAGTGACGCAGTCTCGGCTCACTGCAGCCTCCAACTCCCTGGT T C MPHOSPH9 Ensembl:ENSG00000051825 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1279089276 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17560942 RMVar_hsa_circ_81544,RMVar_hsa_circ_98333,RMVar_hsa_circ_161237,RMVar_hsa_circ_161238 35419 RMVar_ID_35419 Human_SNP_ID_518848969 A-to-I Human chr12 - 123159142 123159142 123159142 AATAATAAAAAAAAATACCTGCCAATGTGATCATTTTTTAAAAGGTGTGGGGTTGTCTTGGCTAA AATAATAAAAAAAAATACCTGCCAATGTGATCGTTTTTTAAAAGGTGTGGGGTTGTCTTGGCTAA T C MPHOSPH9 Ensembl:ENSG00000051825 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2851438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2310521,Human_RBP_ID_3396860 GWAS_ID_3946 RMVar_hsa_circ_81544,RMVar_hsa_circ_98333,RMVar_hsa_circ_161237,RMVar_hsa_circ_161238 35420 RMVar_ID_35420 Human_SNP_ID_518849012 A-to-I Human chr12 - 123159296 123159296 123159296 AGCCAGGCGTGGTAGTGCACGCCTGCAGTCCTAGCTACTCGGGAGGCTGAGGCATGAGAATCGCT AGCCAGGCGTGGTAGTGCACGCCTGCAGTCCTGGCTACTCGGGAGGCTGAGGCATGAGAATCGCT T C MPHOSPH9 Ensembl:ENSG00000051825 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1306643383 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81544,RMVar_hsa_circ_98333,RMVar_hsa_circ_161237,RMVar_hsa_circ_161238 35421 RMVar_ID_35421 Human_SNP_ID_518851337 A-to-I Human chr12 - 123168970 123168970 123168970 TGAAGCAGTAGAATGGTGTGAACCCAAGAGGCAGAGCTTGCCGTGAGCCGAGATCGCGCCACTGC TGAAGCAGTAGAATGGTGTGAACCCAAGAGGCGGAGCTTGCCGTGAGCCGAGATCGCGCCACTGC T C MPHOSPH9 Ensembl:ENSG00000051825 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1375043222 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_428,RMVar_hsa_circ_98333,RMVar_hsa_circ_270777,RMVar_hsa_circ_322344,RMVar_hsa_circ_161238,RMVar_hsa_circ_344902,RMVar_hsa_circ_373021,RMVar_hsa_circ_301697,RMVar_hsa_circ_318400,RMVar_hsa_circ_274631,RMVar_hsa_circ_73008,RMVar_hsa_circ_61129,RMVar_hsa_circ_21414,RMVar_hsa_circ_65180,RMVar_hsa_circ_161240,RMVar_hsa_circ_161242,RMVar_hsa_circ_161244,RMVar_hsa_circ_161245,RMVar_hsa_circ_161243,RMVar_hsa_circ_161241,RMVar_hsa_circ_161239,RMVar_hsa_circ_112150,RMVar_hsa_circ_119361,RMVar_hsa_circ_115396,RMVar_hsa_circ_161248,RMVar_hsa_circ_356741,RMVar_hsa_circ_161249,RMVar_hsa_circ_359049,RMVar_hsa_circ_305866,RMVar_hsa_circ_76789,RMVar_hsa_circ_161250,RMVar_hsa_circ_161251,RMVar_hsa_circ_161253,RMVar_hsa_circ_3423,RMVar_hsa_circ_161254,RMVar_hsa_circ_33029,RMVar_hsa_circ_109269,RMVar_hsa_circ_283203,RMVar_hsa_circ_317105,RMVar_hsa_circ_331295,RMVar_hsa_circ_283259,RMVar_hsa_circ_265552,RMVar_hsa_circ_50157,RMVar_hsa_circ_51309,RMVar_hsa_circ_49297,RMVar_hsa_circ_161256,RMVar_hsa_circ_161257,RMVar_hsa_circ_161258,RMVar_hsa_circ_161255 35422 RMVar_ID_35422 Human_SNP_ID_518853728 A-to-I Human chr12 - 123178661 123178661 123178661 AAATTAGCTGGGCATGGTGGTGCACACCTGTAATCCCTGCTACTCAGGAGGGTGAGGCAGGAGAA AAATTAGCTGGGCATGGTGGTGCACACCTGTAGTCCCTGCTACTCAGGAGGGTGAGGCAGGAGAA T C MPHOSPH9 Ensembl:ENSG00000051825 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs796105201 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_428,RMVar_hsa_circ_98333,RMVar_hsa_circ_270777,RMVar_hsa_circ_161238,RMVar_hsa_circ_344902,RMVar_hsa_circ_373021,RMVar_hsa_circ_301697,RMVar_hsa_circ_318400,RMVar_hsa_circ_274631,RMVar_hsa_circ_73008,RMVar_hsa_circ_61129,RMVar_hsa_circ_21414,RMVar_hsa_circ_65180,RMVar_hsa_circ_161240,RMVar_hsa_circ_161242,RMVar_hsa_circ_161244,RMVar_hsa_circ_161243,RMVar_hsa_circ_161241,RMVar_hsa_circ_161239,RMVar_hsa_circ_112150,RMVar_hsa_circ_119361,RMVar_hsa_circ_115396,RMVar_hsa_circ_161248,RMVar_hsa_circ_356741,RMVar_hsa_circ_161249,RMVar_hsa_circ_359049,RMVar_hsa_circ_305866,RMVar_hsa_circ_76789,RMVar_hsa_circ_161250,RMVar_hsa_circ_161251,RMVar_hsa_circ_161253,RMVar_hsa_circ_3423,RMVar_hsa_circ_161254,RMVar_hsa_circ_33029,RMVar_hsa_circ_109269,RMVar_hsa_circ_283203,RMVar_hsa_circ_317105,RMVar_hsa_circ_331295,RMVar_hsa_circ_283259,RMVar_hsa_circ_265552,RMVar_hsa_circ_50157,RMVar_hsa_circ_49297,RMVar_hsa_circ_317174,RMVar_hsa_circ_161256,RMVar_hsa_circ_161257,RMVar_hsa_circ_161258,RMVar_hsa_circ_161255,RMVar_hsa_circ_369504,RMVar_hsa_circ_290595,RMVar_hsa_circ_294399,RMVar_hsa_circ_272149,RMVar_hsa_circ_161260,RMVar_hsa_circ_9191,RMVar_hsa_circ_33850,RMVar_hsa_circ_161262,RMVar_hsa_circ_6730,RMVar_hsa_circ_161263,RMVar_hsa_circ_161261 35423 RMVar_ID_35423 Human_SNP_ID_518854543 A-to-I Human chr12 - 123182105 123182105 123182105 GAAACCCCGTCTTTACTAAAAATACAAAAATTAGCCGGGCATGGTGGCGTGCGCCTGTAGTCCCA GAAACCCCGTCTTTACTAAAAATACAAAAATTGGCCGGGCATGGTGGCGTGCGCCTGTAGTCCCA T C MPHOSPH9 Ensembl:ENSG00000051825 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1303888225 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_428,RMVar_hsa_circ_98333,RMVar_hsa_circ_270777,RMVar_hsa_circ_161238,RMVar_hsa_circ_344902,RMVar_hsa_circ_373021,RMVar_hsa_circ_318400,RMVar_hsa_circ_274631,RMVar_hsa_circ_73008,RMVar_hsa_circ_61129,RMVar_hsa_circ_3605,RMVar_hsa_circ_21414,RMVar_hsa_circ_65180,RMVar_hsa_circ_161240,RMVar_hsa_circ_161242,RMVar_hsa_circ_161243,RMVar_hsa_circ_161241,RMVar_hsa_circ_161239,RMVar_hsa_circ_112150,RMVar_hsa_circ_115396,RMVar_hsa_circ_161248,RMVar_hsa_circ_356741,RMVar_hsa_circ_161249,RMVar_hsa_circ_359049,RMVar_hsa_circ_305866,RMVar_hsa_circ_76789,RMVar_hsa_circ_161251,RMVar_hsa_circ_161253,RMVar_hsa_circ_3423,RMVar_hsa_circ_161254,RMVar_hsa_circ_33029,RMVar_hsa_circ_109269,RMVar_hsa_circ_317105,RMVar_hsa_circ_283259,RMVar_hsa_circ_265552,RMVar_hsa_circ_50157,RMVar_hsa_circ_49297,RMVar_hsa_circ_161256,RMVar_hsa_circ_161257,RMVar_hsa_circ_161255,RMVar_hsa_circ_369504,RMVar_hsa_circ_290595,RMVar_hsa_circ_294399,RMVar_hsa_circ_272149,RMVar_hsa_circ_9191,RMVar_hsa_circ_33850,RMVar_hsa_circ_161262,RMVar_hsa_circ_6730,RMVar_hsa_circ_161263,RMVar_hsa_circ_161261,RMVar_hsa_circ_123741,RMVar_hsa_circ_335986,RMVar_hsa_circ_331684,RMVar_hsa_circ_314670,RMVar_hsa_circ_25389,RMVar_hsa_circ_50666,RMVar_hsa_circ_161266,RMVar_hsa_circ_161267,RMVar_hsa_circ_161265,RMVar_hsa_circ_115836,RMVar_hsa_circ_161269,RMVar_hsa_circ_4917,RMVar_hsa_circ_161268 35424 RMVar_ID_35424 Human_SNP_ID_518858580 A-to-I Human chr12 - 123197682 123197682 123197682 CGCCTCCCAGGTTCAGGCGATTCTCCTGCCTCAGCCTCCCTAGTAGCTGGGACTACAGGTGCATG CGCCTCCCAGGTTCAGGCGATTCTCCTGCCTCGGCCTCCCTAGTAGCTGGGACTACAGGTGCATG T C MPHOSPH9 Ensembl:ENSG00000051825 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1483018041 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_428,RMVar_hsa_circ_98333,RMVar_hsa_circ_270777,RMVar_hsa_circ_161238,RMVar_hsa_circ_344902,RMVar_hsa_circ_318400,RMVar_hsa_circ_274631,RMVar_hsa_circ_73008,RMVar_hsa_circ_61129,RMVar_hsa_circ_3605,RMVar_hsa_circ_65180,RMVar_hsa_circ_161240,RMVar_hsa_circ_161242,RMVar_hsa_circ_161241,RMVar_hsa_circ_161239,RMVar_hsa_circ_112150,RMVar_hsa_circ_115396,RMVar_hsa_circ_161248,RMVar_hsa_circ_356741,RMVar_hsa_circ_161249,RMVar_hsa_circ_359049,RMVar_hsa_circ_305866,RMVar_hsa_circ_76789,RMVar_hsa_circ_161251,RMVar_hsa_circ_161253,RMVar_hsa_circ_3423,RMVar_hsa_circ_161254,RMVar_hsa_circ_109269,RMVar_hsa_circ_317105,RMVar_hsa_circ_283259,RMVar_hsa_circ_265552,RMVar_hsa_circ_50157,RMVar_hsa_circ_49297,RMVar_hsa_circ_161256,RMVar_hsa_circ_161257,RMVar_hsa_circ_161255,RMVar_hsa_circ_369504,RMVar_hsa_circ_290595,RMVar_hsa_circ_294399,RMVar_hsa_circ_272149,RMVar_hsa_circ_9191,RMVar_hsa_circ_33850,RMVar_hsa_circ_161262,RMVar_hsa_circ_161263,RMVar_hsa_circ_161261,RMVar_hsa_circ_123741,RMVar_hsa_circ_335986,RMVar_hsa_circ_331684,RMVar_hsa_circ_314670,RMVar_hsa_circ_25389,RMVar_hsa_circ_161271,RMVar_hsa_circ_50666,RMVar_hsa_circ_161266,RMVar_hsa_circ_161267,RMVar_hsa_circ_161265,RMVar_hsa_circ_115836,RMVar_hsa_circ_350629,RMVar_hsa_circ_161269,RMVar_hsa_circ_4917,RMVar_hsa_circ_161268,RMVar_hsa_circ_366477,RMVar_hsa_circ_329198,RMVar_hsa_circ_342085,RMVar_hsa_circ_306725,RMVar_hsa_circ_45145,RMVar_hsa_circ_291940,RMVar_hsa_circ_296586,RMVar_hsa_circ_291739,RMVar_hsa_circ_161273,RMVar_hsa_circ_161275,RMVar_hsa_circ_161274,RMVar_hsa_circ_161272,RMVar_hsa_circ_161270 35425 RMVar_ID_35425 Human_SNP_ID_518860210 A-to-I Human chr12 - 123203760 123203760 123203760 AAGATCACTTTAGCCTGGGAGATTGAGGCTGCAGTGAACCATGATCACACCACTGCACTCCAGCC AAGATCACTTTAGCCTGGGAGATTGAGGCTGCGGTGAACCATGATCACACCACTGCACTCCAGCC T C MPHOSPH9 Ensembl:ENSG00000051825 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1476097075 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_428,RMVar_hsa_circ_98333,RMVar_hsa_circ_161238,RMVar_hsa_circ_344902,RMVar_hsa_circ_274631,RMVar_hsa_circ_161240,RMVar_hsa_circ_161239,RMVar_hsa_circ_112150,RMVar_hsa_circ_115396,RMVar_hsa_circ_161248,RMVar_hsa_circ_161249,RMVar_hsa_circ_305866,RMVar_hsa_circ_76789,RMVar_hsa_circ_161251,RMVar_hsa_circ_161254,RMVar_hsa_circ_109269,RMVar_hsa_circ_283259,RMVar_hsa_circ_161255,RMVar_hsa_circ_294399,RMVar_hsa_circ_33850,RMVar_hsa_circ_123741,RMVar_hsa_circ_335986,RMVar_hsa_circ_25389,RMVar_hsa_circ_161271,RMVar_hsa_circ_50666,RMVar_hsa_circ_161267,RMVar_hsa_circ_115836,RMVar_hsa_circ_350629,RMVar_hsa_circ_161269,RMVar_hsa_circ_366477,RMVar_hsa_circ_306725,RMVar_hsa_circ_45145,RMVar_hsa_circ_291940,RMVar_hsa_circ_296586,RMVar_hsa_circ_161273,RMVar_hsa_circ_161272,RMVar_hsa_circ_26213,RMVar_hsa_circ_371106,RMVar_hsa_circ_161270,RMVar_hsa_circ_34604,RMVar_hsa_circ_161279,RMVar_hsa_circ_83435,RMVar_hsa_circ_374801,RMVar_hsa_circ_161277,RMVar_hsa_circ_354704,RMVar_hsa_circ_161278,RMVar_hsa_circ_161280 35426 RMVar_ID_35426 Human_SNP_ID_518860259 A-to-I Human chr12 - 123203982 123203982 123203982 TATTTTCTTACCTCAAAACTTGGCTATTGGCTAGGCGTGGTGGCTCATGCCTGTAATCCCAGCAC TATTTTCTTACCTCAAAACTTGGCTATTGGCTGGGCGTGGTGGCTCATGCCTGTAATCCCAGCAC T C MPHOSPH9 Ensembl:ENSG00000051825 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1486510414 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_428,RMVar_hsa_circ_98333,RMVar_hsa_circ_161238,RMVar_hsa_circ_344902,RMVar_hsa_circ_274631,RMVar_hsa_circ_161240,RMVar_hsa_circ_161239,RMVar_hsa_circ_112150,RMVar_hsa_circ_115396,RMVar_hsa_circ_161248,RMVar_hsa_circ_161249,RMVar_hsa_circ_305866,RMVar_hsa_circ_76789,RMVar_hsa_circ_161251,RMVar_hsa_circ_161254,RMVar_hsa_circ_109269,RMVar_hsa_circ_283259,RMVar_hsa_circ_161255,RMVar_hsa_circ_294399,RMVar_hsa_circ_33850,RMVar_hsa_circ_123741,RMVar_hsa_circ_335986,RMVar_hsa_circ_25389,RMVar_hsa_circ_161271,RMVar_hsa_circ_50666,RMVar_hsa_circ_161267,RMVar_hsa_circ_115836,RMVar_hsa_circ_350629,RMVar_hsa_circ_161269,RMVar_hsa_circ_366477,RMVar_hsa_circ_306725,RMVar_hsa_circ_45145,RMVar_hsa_circ_291940,RMVar_hsa_circ_296586,RMVar_hsa_circ_161273,RMVar_hsa_circ_161272,RMVar_hsa_circ_26213,RMVar_hsa_circ_371106,RMVar_hsa_circ_161270,RMVar_hsa_circ_34604,RMVar_hsa_circ_161279,RMVar_hsa_circ_83435,RMVar_hsa_circ_374801,RMVar_hsa_circ_161277,RMVar_hsa_circ_354704,RMVar_hsa_circ_161278,RMVar_hsa_circ_161280 35427 RMVar_ID_35427 Human_SNP_ID_518860316 A-to-I Human chr12 - 123204180 123204180 123204180 CTCCTGCCTCAGCTTCCCTTGTAGCTGGGATTACAGGCATGCGCCACCATGCCTGGCTAATTTTG CTCCTGCCTCAGCTTCCCTTGTAGCTGGGATTCCAGGCATGCGCCACCATGCCTGGCTAATTTTG T G MPHOSPH9 Ensembl:ENSG00000051825 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1397366622 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_428,RMVar_hsa_circ_98333,RMVar_hsa_circ_161238,RMVar_hsa_circ_344902,RMVar_hsa_circ_274631,RMVar_hsa_circ_161240,RMVar_hsa_circ_161239,RMVar_hsa_circ_112150,RMVar_hsa_circ_115396,RMVar_hsa_circ_161248,RMVar_hsa_circ_161249,RMVar_hsa_circ_305866,RMVar_hsa_circ_76789,RMVar_hsa_circ_161251,RMVar_hsa_circ_161254,RMVar_hsa_circ_109269,RMVar_hsa_circ_283259,RMVar_hsa_circ_161255,RMVar_hsa_circ_294399,RMVar_hsa_circ_33850,RMVar_hsa_circ_123741,RMVar_hsa_circ_335986,RMVar_hsa_circ_25389,RMVar_hsa_circ_161271,RMVar_hsa_circ_50666,RMVar_hsa_circ_161267,RMVar_hsa_circ_115836,RMVar_hsa_circ_350629,RMVar_hsa_circ_161269,RMVar_hsa_circ_366477,RMVar_hsa_circ_306725,RMVar_hsa_circ_45145,RMVar_hsa_circ_291940,RMVar_hsa_circ_296586,RMVar_hsa_circ_161273,RMVar_hsa_circ_161272,RMVar_hsa_circ_26213,RMVar_hsa_circ_371106,RMVar_hsa_circ_161270,RMVar_hsa_circ_34604,RMVar_hsa_circ_161279,RMVar_hsa_circ_83435,RMVar_hsa_circ_374801,RMVar_hsa_circ_161277,RMVar_hsa_circ_354704,RMVar_hsa_circ_161278,RMVar_hsa_circ_161280 35428 RMVar_ID_35428 Human_SNP_ID_518860502 A-to-I Human chr12 - 123204839 123204839 123204839 TTGCTCTGTCGCCCAGGCTAGAGTGAAGGAGTACAGTGGCATGATCCCAACTCACTGCAACCTCT TTGCTCTGTCGCCCAGGCTAGAGTGAAGGAGTGCAGTGGCATGATCCCAACTCACTGCAACCTCT T C MPHOSPH9 Ensembl:ENSG00000051825 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2695479 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11862932,Human_RBP_ID_19733333 GWAS_ID_3947,GWAS_ID_3948,GWAS_ID_3949,GWAS_ID_3950,GWAS_ID_3951,GWAS_ID_3952,GWAS_ID_3953,GWAS_ID_3954,GWAS_ID_3955,GWAS_ID_3956,GWAS_ID_3957,GWAS_ID_3958,GWAS_ID_3959,GWAS_ID_3960,GWAS_ID_3961,GWAS_ID_3962,GWAS_ID_3963,GWAS_ID_3964,GWAS_ID_3965,GWAS_ID_3966,GWAS_ID_3967,GWAS_ID_3968,GWAS_ID_3969,GWAS_ID_3970,GWAS_ID_3971,GWAS_ID_3972,GWAS_ID_3973,GWAS_ID_3974,GWAS_ID_3975,GWAS_ID_3976,GWAS_ID_3977,GWAS_ID_3978,GWAS_ID_3979,GWAS_ID_3980,GWAS_ID_3981,GWAS_ID_3982,GWAS_ID_3983,GWAS_ID_3984,GWAS_ID_3985,GWAS_ID_3986,GWAS_ID_3987,GWAS_ID_3988,GWAS_ID_3989,GWAS_ID_3990,GWAS_ID_3991,GWAS_ID_3992,GWAS_ID_3993,GWAS_ID_3994,GWAS_ID_3995,GWAS_ID_3996,GWAS_ID_3997,GWAS_ID_3998,GWAS_ID_3999,GWAS_ID_4000,GWAS_ID_4001,GWAS_ID_4002,GWAS_ID_4003,GWAS_ID_4004,GWAS_ID_4005,GWAS_ID_4006,GWAS_ID_4007,GWAS_ID_4008,GWAS_ID_4009,GWAS_ID_4010,GWAS_ID_4011,GWAS_ID_4012,GWAS_ID_4013,GWAS_ID_4014,GWAS_ID_4015,GWAS_ID_4016,GWAS_ID_4017,GWAS_ID_4018,GWAS_ID_4019,GWAS_ID_4020,GWAS_ID_4021,GWAS_ID_4022,GWAS_ID_4023,GWAS_ID_4024,GWAS_ID_4025,GWAS_ID_4026,GWAS_ID_4027,GWAS_ID_4028,GWAS_ID_4029,GWAS_ID_4030,GWAS_ID_4031,GWAS_ID_4032,GWAS_ID_4033 RMVar_hsa_circ_428,RMVar_hsa_circ_98333,RMVar_hsa_circ_161238,RMVar_hsa_circ_344902,RMVar_hsa_circ_274631,RMVar_hsa_circ_161240,RMVar_hsa_circ_161239,RMVar_hsa_circ_112150,RMVar_hsa_circ_115396,RMVar_hsa_circ_161248,RMVar_hsa_circ_161249,RMVar_hsa_circ_305866,RMVar_hsa_circ_76789,RMVar_hsa_circ_161251,RMVar_hsa_circ_161254,RMVar_hsa_circ_109269,RMVar_hsa_circ_283259,RMVar_hsa_circ_161255,RMVar_hsa_circ_294399,RMVar_hsa_circ_33850,RMVar_hsa_circ_123741,RMVar_hsa_circ_335986,RMVar_hsa_circ_25389,RMVar_hsa_circ_161271,RMVar_hsa_circ_50666,RMVar_hsa_circ_161267,RMVar_hsa_circ_115836,RMVar_hsa_circ_350629,RMVar_hsa_circ_161269,RMVar_hsa_circ_366477,RMVar_hsa_circ_306725,RMVar_hsa_circ_45145,RMVar_hsa_circ_291940,RMVar_hsa_circ_296586,RMVar_hsa_circ_161273,RMVar_hsa_circ_161272,RMVar_hsa_circ_26213,RMVar_hsa_circ_371106,RMVar_hsa_circ_161270,RMVar_hsa_circ_34604,RMVar_hsa_circ_161279,RMVar_hsa_circ_83435,RMVar_hsa_circ_374801,RMVar_hsa_circ_161277,RMVar_hsa_circ_354704,RMVar_hsa_circ_161278,RMVar_hsa_circ_161280 35429 RMVar_ID_35429 Human_SNP_ID_518860853 A-to-I Human chr12 - 123206278 123206278 123206278 TTTTTTTTGTTTGTTTGTTTTTAGTAGAGGCAAGGTCTCTCTATGTTGCCCAAGCTGGTCTCTCA TTTTTTTTGTTTGTTTGTTTTTAGTAGAGGCAGGGTCTCTCTATGTTGCCCAAGCTGGTCTCTCA T C MPHOSPH9 Ensembl:ENSG00000051825 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs573904669 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6147760 RMVar_hsa_circ_428,RMVar_hsa_circ_98333,RMVar_hsa_circ_161238,RMVar_hsa_circ_344902,RMVar_hsa_circ_274631,RMVar_hsa_circ_161240,RMVar_hsa_circ_161239,RMVar_hsa_circ_112150,RMVar_hsa_circ_115396,RMVar_hsa_circ_161248,RMVar_hsa_circ_161249,RMVar_hsa_circ_305866,RMVar_hsa_circ_76789,RMVar_hsa_circ_161251,RMVar_hsa_circ_161254,RMVar_hsa_circ_109269,RMVar_hsa_circ_283259,RMVar_hsa_circ_161255,RMVar_hsa_circ_294399,RMVar_hsa_circ_33850,RMVar_hsa_circ_123741,RMVar_hsa_circ_335986,RMVar_hsa_circ_25389,RMVar_hsa_circ_161271,RMVar_hsa_circ_50666,RMVar_hsa_circ_161267,RMVar_hsa_circ_115836,RMVar_hsa_circ_350629,RMVar_hsa_circ_161269,RMVar_hsa_circ_366477,RMVar_hsa_circ_306725,RMVar_hsa_circ_45145,RMVar_hsa_circ_291940,RMVar_hsa_circ_296586,RMVar_hsa_circ_161273,RMVar_hsa_circ_161272,RMVar_hsa_circ_26213,RMVar_hsa_circ_371106,RMVar_hsa_circ_161270,RMVar_hsa_circ_34604,RMVar_hsa_circ_161279,RMVar_hsa_circ_83435,RMVar_hsa_circ_374801,RMVar_hsa_circ_161277,RMVar_hsa_circ_354704,RMVar_hsa_circ_161278,RMVar_hsa_circ_161280 35430 RMVar_ID_35430 Human_SNP_ID_518860985 A-to-I Human chr12 - 123206679 123206679 123206679 TCGATCTCCTGACCTTGTGACCCACCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG TCGATCTCCTGACCTTGTGACCCACCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG T C MPHOSPH9 Ensembl:ENSG00000051825 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1210133898 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_428,RMVar_hsa_circ_98333,RMVar_hsa_circ_161238,RMVar_hsa_circ_344902,RMVar_hsa_circ_274631,RMVar_hsa_circ_161240,RMVar_hsa_circ_161239,RMVar_hsa_circ_112150,RMVar_hsa_circ_115396,RMVar_hsa_circ_161248,RMVar_hsa_circ_161249,RMVar_hsa_circ_305866,RMVar_hsa_circ_76789,RMVar_hsa_circ_161251,RMVar_hsa_circ_161254,RMVar_hsa_circ_109269,RMVar_hsa_circ_283259,RMVar_hsa_circ_161255,RMVar_hsa_circ_294399,RMVar_hsa_circ_33850,RMVar_hsa_circ_123741,RMVar_hsa_circ_335986,RMVar_hsa_circ_25389,RMVar_hsa_circ_161271,RMVar_hsa_circ_50666,RMVar_hsa_circ_161267,RMVar_hsa_circ_115836,RMVar_hsa_circ_350629,RMVar_hsa_circ_161269,RMVar_hsa_circ_366477,RMVar_hsa_circ_306725,RMVar_hsa_circ_45145,RMVar_hsa_circ_291940,RMVar_hsa_circ_296586,RMVar_hsa_circ_161273,RMVar_hsa_circ_161272,RMVar_hsa_circ_26213,RMVar_hsa_circ_371106,RMVar_hsa_circ_161270,RMVar_hsa_circ_34604,RMVar_hsa_circ_161279,RMVar_hsa_circ_83435,RMVar_hsa_circ_374801,RMVar_hsa_circ_161277,RMVar_hsa_circ_354704,RMVar_hsa_circ_161278,RMVar_hsa_circ_161280 35431 RMVar_ID_35431 Human_SNP_ID_518861591 A-to-I Human chr12 - 123208864 123208864 123208864 CTGGCTGGCTTGAGCTGGGCATCATAGTTTACACCTGTAATCCTTGTACTTTGGGAGGCTGAGGT CTGGCTGGCTTGAGCTGGGCATCATAGTTTACGCCTGTAATCCTTGTACTTTGGGAGGCTGAGGT T C MPHOSPH9 Ensembl:ENSG00000051825 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1310683923 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11863102,Human_RBP_ID_17561568 RMVar_hsa_circ_428,RMVar_hsa_circ_98333,RMVar_hsa_circ_161238,RMVar_hsa_circ_344902,RMVar_hsa_circ_274631,RMVar_hsa_circ_161240,RMVar_hsa_circ_161239,RMVar_hsa_circ_112150,RMVar_hsa_circ_115396,RMVar_hsa_circ_161248,RMVar_hsa_circ_161249,RMVar_hsa_circ_305866,RMVar_hsa_circ_76789,RMVar_hsa_circ_161251,RMVar_hsa_circ_161254,RMVar_hsa_circ_109269,RMVar_hsa_circ_283259,RMVar_hsa_circ_161255,RMVar_hsa_circ_294399,RMVar_hsa_circ_33850,RMVar_hsa_circ_123741,RMVar_hsa_circ_335986,RMVar_hsa_circ_25389,RMVar_hsa_circ_161271,RMVar_hsa_circ_50666,RMVar_hsa_circ_161267,RMVar_hsa_circ_115836,RMVar_hsa_circ_350629,RMVar_hsa_circ_161269,RMVar_hsa_circ_366477,RMVar_hsa_circ_306725,RMVar_hsa_circ_45145,RMVar_hsa_circ_291940,RMVar_hsa_circ_296586,RMVar_hsa_circ_161273,RMVar_hsa_circ_161272,RMVar_hsa_circ_26213,RMVar_hsa_circ_371106,RMVar_hsa_circ_161270,RMVar_hsa_circ_34604,RMVar_hsa_circ_161279,RMVar_hsa_circ_83435,RMVar_hsa_circ_374801,RMVar_hsa_circ_161277,RMVar_hsa_circ_354704,RMVar_hsa_circ_161278,RMVar_hsa_circ_161280 35432 RMVar_ID_35432 Human_SNP_ID_518861593 A-to-I Human chr12 - 123208873 123208873 123208873 TAAAAAATTCTGGCTGGCTTGAGCTGGGCATCATAGTTTACACCTGTAATCCTTGTACTTTGGGA TAAAAAATTCTGGCTGGCTTGAGCTGGGCATCTTAGTTTACACCTGTAATCCTTGTACTTTGGGA T A MPHOSPH9 Ensembl:ENSG00000051825 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11057192 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11863102,Human_RBP_ID_17561568 GWAS_ID_4034,GWAS_ID_4035,GWAS_ID_4036,GWAS_ID_4037,GWAS_ID_4038,GWAS_ID_4039,GWAS_ID_4040,GWAS_ID_4041 RMVar_hsa_circ_428,RMVar_hsa_circ_98333,RMVar_hsa_circ_161238,RMVar_hsa_circ_344902,RMVar_hsa_circ_274631,RMVar_hsa_circ_161240,RMVar_hsa_circ_161239,RMVar_hsa_circ_112150,RMVar_hsa_circ_115396,RMVar_hsa_circ_161248,RMVar_hsa_circ_161249,RMVar_hsa_circ_305866,RMVar_hsa_circ_76789,RMVar_hsa_circ_161251,RMVar_hsa_circ_161254,RMVar_hsa_circ_109269,RMVar_hsa_circ_283259,RMVar_hsa_circ_161255,RMVar_hsa_circ_294399,RMVar_hsa_circ_33850,RMVar_hsa_circ_123741,RMVar_hsa_circ_335986,RMVar_hsa_circ_25389,RMVar_hsa_circ_161271,RMVar_hsa_circ_50666,RMVar_hsa_circ_161267,RMVar_hsa_circ_115836,RMVar_hsa_circ_350629,RMVar_hsa_circ_161269,RMVar_hsa_circ_366477,RMVar_hsa_circ_306725,RMVar_hsa_circ_45145,RMVar_hsa_circ_291940,RMVar_hsa_circ_296586,RMVar_hsa_circ_161273,RMVar_hsa_circ_161272,RMVar_hsa_circ_26213,RMVar_hsa_circ_371106,RMVar_hsa_circ_161270,RMVar_hsa_circ_34604,RMVar_hsa_circ_161279,RMVar_hsa_circ_83435,RMVar_hsa_circ_374801,RMVar_hsa_circ_161277,RMVar_hsa_circ_354704,RMVar_hsa_circ_161278,RMVar_hsa_circ_161280 35433 RMVar_ID_35433 Human_SNP_ID_518861594 A-to-I Human chr12 - 123208873 123208873 123208873 TAAAAAATTCTGGCTGGCTTGAGCTGGGCATCATAGTTTACACCTGTAATCCTTGTACTTTGGGA TAAAAAATTCTGGCTGGCTTGAGCTGGGCATCGTAGTTTACACCTGTAATCCTTGTACTTTGGGA T C MPHOSPH9 Ensembl:ENSG00000051825 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11057192 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11863102,Human_RBP_ID_17561568 GWAS_ID_4034,GWAS_ID_4035,GWAS_ID_4036,GWAS_ID_4037,GWAS_ID_4038,GWAS_ID_4039,GWAS_ID_4040,GWAS_ID_4041 RMVar_hsa_circ_428,RMVar_hsa_circ_98333,RMVar_hsa_circ_161238,RMVar_hsa_circ_344902,RMVar_hsa_circ_274631,RMVar_hsa_circ_161240,RMVar_hsa_circ_161239,RMVar_hsa_circ_112150,RMVar_hsa_circ_115396,RMVar_hsa_circ_161248,RMVar_hsa_circ_161249,RMVar_hsa_circ_305866,RMVar_hsa_circ_76789,RMVar_hsa_circ_161251,RMVar_hsa_circ_161254,RMVar_hsa_circ_109269,RMVar_hsa_circ_283259,RMVar_hsa_circ_161255,RMVar_hsa_circ_294399,RMVar_hsa_circ_33850,RMVar_hsa_circ_123741,RMVar_hsa_circ_335986,RMVar_hsa_circ_25389,RMVar_hsa_circ_161271,RMVar_hsa_circ_50666,RMVar_hsa_circ_161267,RMVar_hsa_circ_115836,RMVar_hsa_circ_350629,RMVar_hsa_circ_161269,RMVar_hsa_circ_366477,RMVar_hsa_circ_306725,RMVar_hsa_circ_45145,RMVar_hsa_circ_291940,RMVar_hsa_circ_296586,RMVar_hsa_circ_161273,RMVar_hsa_circ_161272,RMVar_hsa_circ_26213,RMVar_hsa_circ_371106,RMVar_hsa_circ_161270,RMVar_hsa_circ_34604,RMVar_hsa_circ_161279,RMVar_hsa_circ_83435,RMVar_hsa_circ_374801,RMVar_hsa_circ_161277,RMVar_hsa_circ_354704,RMVar_hsa_circ_161278,RMVar_hsa_circ_161280 35434 RMVar_ID_35434 Human_SNP_ID_518861623 A-to-I Human chr12 - 123208968 123208968 123208968 AGATGGTGCCACTGCACTCCAGCCTGGGTGACAGAGCGAGACTCCGCCTCAGCAAAAACAACAAC AGATGGTGCCACTGCACTCCAGCCTGGGTGACGGAGCGAGACTCCGCCTCAGCAAAAACAACAAC T C MPHOSPH9 Ensembl:ENSG00000051825 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1368611623 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_428,RMVar_hsa_circ_98333,RMVar_hsa_circ_161238,RMVar_hsa_circ_344902,RMVar_hsa_circ_274631,RMVar_hsa_circ_161240,RMVar_hsa_circ_161239,RMVar_hsa_circ_112150,RMVar_hsa_circ_115396,RMVar_hsa_circ_161248,RMVar_hsa_circ_161249,RMVar_hsa_circ_305866,RMVar_hsa_circ_76789,RMVar_hsa_circ_161251,RMVar_hsa_circ_161254,RMVar_hsa_circ_109269,RMVar_hsa_circ_283259,RMVar_hsa_circ_161255,RMVar_hsa_circ_294399,RMVar_hsa_circ_33850,RMVar_hsa_circ_123741,RMVar_hsa_circ_335986,RMVar_hsa_circ_25389,RMVar_hsa_circ_161271,RMVar_hsa_circ_50666,RMVar_hsa_circ_161267,RMVar_hsa_circ_115836,RMVar_hsa_circ_350629,RMVar_hsa_circ_161269,RMVar_hsa_circ_366477,RMVar_hsa_circ_306725,RMVar_hsa_circ_45145,RMVar_hsa_circ_291940,RMVar_hsa_circ_296586,RMVar_hsa_circ_161273,RMVar_hsa_circ_161272,RMVar_hsa_circ_26213,RMVar_hsa_circ_371106,RMVar_hsa_circ_161270,RMVar_hsa_circ_34604,RMVar_hsa_circ_161279,RMVar_hsa_circ_83435,RMVar_hsa_circ_374801,RMVar_hsa_circ_161277,RMVar_hsa_circ_354704,RMVar_hsa_circ_161278,RMVar_hsa_circ_161280 35435 RMVar_ID_35435 Human_SNP_ID_518861763 A-to-I Human chr12 - 123209518 123209518 123209518 CTGTTCATCCCAGCTATTTGGGAGGCTGAGGCAGGAGAATCACTTGAACCTGGGAGGTGGAGGTT CTGTTCATCCCAGCTATTTGGGAGGCTGAGGCGGGAGAATCACTTGAACCTGGGAGGTGGAGGTT T C MPHOSPH9 Ensembl:ENSG00000051825 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1380052971 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_428,RMVar_hsa_circ_98333,RMVar_hsa_circ_161238,RMVar_hsa_circ_344902,RMVar_hsa_circ_274631,RMVar_hsa_circ_161240,RMVar_hsa_circ_161239,RMVar_hsa_circ_112150,RMVar_hsa_circ_115396,RMVar_hsa_circ_161248,RMVar_hsa_circ_161249,RMVar_hsa_circ_305866,RMVar_hsa_circ_76789,RMVar_hsa_circ_161251,RMVar_hsa_circ_161254,RMVar_hsa_circ_109269,RMVar_hsa_circ_283259,RMVar_hsa_circ_161255,RMVar_hsa_circ_294399,RMVar_hsa_circ_33850,RMVar_hsa_circ_123741,RMVar_hsa_circ_335986,RMVar_hsa_circ_25389,RMVar_hsa_circ_161271,RMVar_hsa_circ_50666,RMVar_hsa_circ_161267,RMVar_hsa_circ_115836,RMVar_hsa_circ_350629,RMVar_hsa_circ_161269,RMVar_hsa_circ_366477,RMVar_hsa_circ_306725,RMVar_hsa_circ_45145,RMVar_hsa_circ_291940,RMVar_hsa_circ_296586,RMVar_hsa_circ_161273,RMVar_hsa_circ_161272,RMVar_hsa_circ_26213,RMVar_hsa_circ_371106,RMVar_hsa_circ_161270,RMVar_hsa_circ_34604,RMVar_hsa_circ_161279,RMVar_hsa_circ_83435,RMVar_hsa_circ_374801,RMVar_hsa_circ_161277,RMVar_hsa_circ_354704,RMVar_hsa_circ_161278,RMVar_hsa_circ_161280 35436 RMVar_ID_35436 Human_SNP_ID_518861799 A-to-I Human chr12 - 123209652 123209652 123209652 TAATCTCGGCACTTTGGGAAGCTGAAGTGGGCAGACCATCTGAGGTAAGGAGTTCGAGACCAGCC TAATCTCGGCACTTTGGGAAGCTGAAGTGGGCGGACCATCTGAGGTAAGGAGTTCGAGACCAGCC T C MPHOSPH9 Ensembl:ENSG00000051825 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1186004135 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6147789 RMVar_hsa_circ_428,RMVar_hsa_circ_98333,RMVar_hsa_circ_161238,RMVar_hsa_circ_344902,RMVar_hsa_circ_274631,RMVar_hsa_circ_161240,RMVar_hsa_circ_161239,RMVar_hsa_circ_112150,RMVar_hsa_circ_115396,RMVar_hsa_circ_161248,RMVar_hsa_circ_161249,RMVar_hsa_circ_305866,RMVar_hsa_circ_76789,RMVar_hsa_circ_161251,RMVar_hsa_circ_161254,RMVar_hsa_circ_109269,RMVar_hsa_circ_283259,RMVar_hsa_circ_161255,RMVar_hsa_circ_294399,RMVar_hsa_circ_33850,RMVar_hsa_circ_123741,RMVar_hsa_circ_335986,RMVar_hsa_circ_25389,RMVar_hsa_circ_161271,RMVar_hsa_circ_50666,RMVar_hsa_circ_161267,RMVar_hsa_circ_115836,RMVar_hsa_circ_350629,RMVar_hsa_circ_161269,RMVar_hsa_circ_366477,RMVar_hsa_circ_306725,RMVar_hsa_circ_45145,RMVar_hsa_circ_291940,RMVar_hsa_circ_296586,RMVar_hsa_circ_161273,RMVar_hsa_circ_161272,RMVar_hsa_circ_26213,RMVar_hsa_circ_371106,RMVar_hsa_circ_161270,RMVar_hsa_circ_34604,RMVar_hsa_circ_161279,RMVar_hsa_circ_83435,RMVar_hsa_circ_374801,RMVar_hsa_circ_161277,RMVar_hsa_circ_354704,RMVar_hsa_circ_161278,RMVar_hsa_circ_161280 35437 RMVar_ID_35437 Human_SNP_ID_518862066 A-to-I Human chr12 - 123210530 123210530 123210530 TGCCACCACACCTGGCTGATTTTTGGATTTTTAGTAGAGATGGGGCTTCACCACGTTGGCCAGGC TGCCACCACACCTGGCTGATTTTTGGATTTTTGGTAGAGATGGGGCTTCACCACGTTGGCCAGGC T C MPHOSPH9 Ensembl:ENSG00000051825 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs773982127 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_428,RMVar_hsa_circ_98333,RMVar_hsa_circ_161238,RMVar_hsa_circ_344902,RMVar_hsa_circ_274631,RMVar_hsa_circ_14880,RMVar_hsa_circ_161240,RMVar_hsa_circ_161239,RMVar_hsa_circ_112150,RMVar_hsa_circ_115396,RMVar_hsa_circ_161248,RMVar_hsa_circ_161249,RMVar_hsa_circ_305866,RMVar_hsa_circ_76789,RMVar_hsa_circ_161251,RMVar_hsa_circ_161254,RMVar_hsa_circ_109269,RMVar_hsa_circ_283259,RMVar_hsa_circ_161255,RMVar_hsa_circ_294399,RMVar_hsa_circ_33850,RMVar_hsa_circ_123741,RMVar_hsa_circ_335986,RMVar_hsa_circ_25389,RMVar_hsa_circ_161271,RMVar_hsa_circ_50666,RMVar_hsa_circ_161267,RMVar_hsa_circ_115836,RMVar_hsa_circ_161269,RMVar_hsa_circ_366477,RMVar_hsa_circ_306725,RMVar_hsa_circ_45145,RMVar_hsa_circ_291940,RMVar_hsa_circ_296586,RMVar_hsa_circ_161272,RMVar_hsa_circ_26213,RMVar_hsa_circ_371106,RMVar_hsa_circ_161270,RMVar_hsa_circ_34604,RMVar_hsa_circ_374801,RMVar_hsa_circ_161277,RMVar_hsa_circ_354704,RMVar_hsa_circ_161278,RMVar_hsa_circ_291199,RMVar_hsa_circ_320597,RMVar_hsa_circ_322888,RMVar_hsa_circ_305935,RMVar_hsa_circ_279443,RMVar_hsa_circ_161282,RMVar_hsa_circ_161284,RMVar_hsa_circ_161285,RMVar_hsa_circ_161283,RMVar_hsa_circ_161281 35438 RMVar_ID_35438 Human_SNP_ID_518865981 A-to-I Human chr12 - 123225261 123225242 123225261 TTTTGCATTTTTTGTTGAGACAAGGTTTTGCTATGTTGCCCAGGTTAGTCTTGAACTCATGAACT TTTTGCATTTTTTGTTGAGACAAGGTTTTGCT___________________TGAACTCATGAACT AAGACTAACCTGGGCAACAT A MPHOSPH9 Ensembl:ENSG00000051825 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1565976286 Functional Loss DEL dbSNP153 33..51 33 - - - Human_RBP_ID_11863398 RMVar_hsa_circ_14880,RMVar_hsa_circ_33850,RMVar_hsa_circ_335986,RMVar_hsa_circ_161271,RMVar_hsa_circ_50666,RMVar_hsa_circ_306725,RMVar_hsa_circ_45145,RMVar_hsa_circ_296586,RMVar_hsa_circ_161270,RMVar_hsa_circ_34604,RMVar_hsa_circ_322888,RMVar_hsa_circ_305935,RMVar_hsa_circ_4426,RMVar_hsa_circ_161284,RMVar_hsa_circ_161285,RMVar_hsa_circ_338008,RMVar_hsa_circ_318454,RMVar_hsa_circ_318882,RMVar_hsa_circ_51667,RMVar_hsa_circ_161293,RMVar_hsa_circ_161294,RMVar_hsa_circ_53907,RMVar_hsa_circ_39255,RMVar_hsa_circ_297197,RMVar_hsa_circ_161297,RMVar_hsa_circ_290606,RMVar_hsa_circ_297260,RMVar_hsa_circ_349765 35439 RMVar_ID_35439 Human_SNP_ID_518865982 A-to-I Human chr12 - 123225261 123225247 123225262 TTTTGCATTTTTTGTTGAGACAAGGTTTTGCTATGTTGCCCAGGTTAGTCTTGAACTCATGAACT TTTTGCATTTTTTGTTGAGACAAGGTTTTGC_______________AGTCTTGAACTCATGAACT TAACCTGGGCAACATA T MPHOSPH9 Ensembl:ENSG00000051825 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs527470137 Functional Loss DEL dbSNP153 32..46 33 - - - Human_RBP_ID_11863398 RMVar_hsa_circ_14880,RMVar_hsa_circ_33850,RMVar_hsa_circ_335986,RMVar_hsa_circ_161271,RMVar_hsa_circ_50666,RMVar_hsa_circ_306725,RMVar_hsa_circ_45145,RMVar_hsa_circ_296586,RMVar_hsa_circ_161270,RMVar_hsa_circ_34604,RMVar_hsa_circ_322888,RMVar_hsa_circ_305935,RMVar_hsa_circ_4426,RMVar_hsa_circ_161284,RMVar_hsa_circ_161285,RMVar_hsa_circ_338008,RMVar_hsa_circ_318454,RMVar_hsa_circ_318882,RMVar_hsa_circ_51667,RMVar_hsa_circ_161293,RMVar_hsa_circ_161294,RMVar_hsa_circ_53907,RMVar_hsa_circ_39255,RMVar_hsa_circ_297197,RMVar_hsa_circ_161297,RMVar_hsa_circ_290606,RMVar_hsa_circ_297260,RMVar_hsa_circ_349765 35440 RMVar_ID_35440 Human_SNP_ID_518865983 A-to-I Human chr12 - 123225247 123225247 123225247 TTGAGACAAGGTTTTGCTATGTTGCCCAGGTTAGTCTTGAACTCATGAACTCAAATGATCCACCC TTGAGACAAGGTTTTGCTATGTTGCCCAGGTTGGTCTTGAACTCATGAACTCAAATGATCCACCC T C MPHOSPH9 Ensembl:ENSG00000051825 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs979370001 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11863398 RMVar_hsa_circ_14880,RMVar_hsa_circ_33850,RMVar_hsa_circ_335986,RMVar_hsa_circ_161271,RMVar_hsa_circ_50666,RMVar_hsa_circ_306725,RMVar_hsa_circ_45145,RMVar_hsa_circ_296586,RMVar_hsa_circ_161270,RMVar_hsa_circ_34604,RMVar_hsa_circ_322888,RMVar_hsa_circ_305935,RMVar_hsa_circ_4426,RMVar_hsa_circ_161284,RMVar_hsa_circ_161285,RMVar_hsa_circ_338008,RMVar_hsa_circ_318454,RMVar_hsa_circ_318882,RMVar_hsa_circ_51667,RMVar_hsa_circ_161293,RMVar_hsa_circ_161294,RMVar_hsa_circ_53907,RMVar_hsa_circ_39255,RMVar_hsa_circ_297197,RMVar_hsa_circ_161297,RMVar_hsa_circ_290606,RMVar_hsa_circ_297260,RMVar_hsa_circ_349765 35441 RMVar_ID_35441 Human_SNP_ID_518868449 A-to-I Human chr12 + 123235491 123235491 123235491 GGTTCACGCCATTCTCCTGCCTTAGCCTCCCTAGTAGCTGAGACTACAGGTGCCTGCCACCAGGC GGTTCACGCCATTCTCCTGCCTTAGCCTCCCTGGTAGCTGAGACTACAGGTGCCTGCCACCAGGC A G C12orf65 Ensembl:ENSG00000130921 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1270361421 Functional Loss SNV dbSNP153 33..33 33 - - - 35442 RMVar_ID_35442 Human_SNP_ID_518874661 A-to-I Human chr12 - 123258323 123258323 123258323 CAGTCTTGCTCTGTTGCTCACGCTGGAGTGCAATGGCGCAATCTTGGCTCACTGCAACCTCGCCT CAGTCTTGCTCTGTTGCTCACGCTGGAGTGCAGTGGCGCAATCTTGGCTCACTGCAACCTCGCCT T C CDK2AP1 Ensembl:ENSG00000111328 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1257567919 Functional Loss SNV dbSNP153 33..33 33 - - - 35443 RMVar_ID_35443 Human_SNP_ID_518877187 A-to-I Human chr12 - 123267197 123267197 123267197 CAGCTGCTCAGTGACTACGGGCCACCGTCCCTAGGCTACACCCAGGTATGTCAATGGGGGTGATG CAGCTGCTCAGTGACTACGGGCCACCGTCCCTGGGCTACACCCAGGTATGTCAATGGGGGTGATG T C CDK2AP1 Ensembl:ENSG00000111328 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1366423838 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_413786,Human_RBP_ID_4247971 Human_Splice_Rec_1439444,Human_Splice_Rec_1439445,Human_Splice_Rec_1439476,Human_Splice_Rec_1439477,Human_Splice_Rec_1439482,Human_Splice_Rec_1439483,Human_Splice_Rec_1439488,Human_Splice_Rec_1439489,Human_Splice_Rec_1439494,Human_Splice_Rec_1439495,Human_Splice_Rec_1439499,Human_Splice_Rec_1439504,Human_Splice_Rec_1439505,Human_Splice_Rec_1439510,Human_Splice_Rec_1439511 RMVar_hsa_circ_285668 35444 RMVar_ID_35444 Human_SNP_ID_518888069 A-to-I Human chr12 - 123300767 123300767 123300767 TTAGTAGAGACAGGGTTTTACCATGTTGGCCAAGCTGGTCTCGAACTCCTGACTTTGTGATCTGC TTAGTAGAGACAGGGTTTTACCATGTTGGCCACGCTGGTCTCGAACTCCTGACTTTGTGATCTGC T G SBNO1 Ensembl:ENSG00000139697 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs964866938 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_161302,RMVar_hsa_circ_97966,RMVar_hsa_circ_265655,RMVar_hsa_circ_161305,RMVar_hsa_circ_93677,RMVar_hsa_circ_332105,RMVar_hsa_circ_334493,RMVar_hsa_circ_96621,RMVar_hsa_circ_161306,RMVar_hsa_circ_161307 35445 RMVar_ID_35445 Human_SNP_ID_518888088 A-to-I Human chr12 - 123300859 123300859 123300859 CATCTCCCAGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCCGAGTAGCTAGGACTACAGTGCCTGC CATCTCCCAGGTTCAAGCAGTTCTCCTGCCTCGGCCTCCCGAGTAGCTAGGACTACAGTGCCTGC T C SBNO1 Ensembl:ENSG00000139697 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1240378358 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_161302,RMVar_hsa_circ_97966,RMVar_hsa_circ_265655,RMVar_hsa_circ_161305,RMVar_hsa_circ_93677,RMVar_hsa_circ_332105,RMVar_hsa_circ_334493,RMVar_hsa_circ_96621,RMVar_hsa_circ_161306,RMVar_hsa_circ_161307 35446 RMVar_ID_35446 Human_SNP_ID_518888093 A-to-I Human chr12 - 123300876 123300876 123300876 CAGCTCACTGCAACCTCCATCTCCCAGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCCGAGTAGCT CAGCTCACTGCAACCTCCATCTCCCAGGTTCACGCAGTTCTCCTGCCTCAGCCTCCCGAGTAGCT T G SBNO1 Ensembl:ENSG00000139697 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1448376682 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_161302,RMVar_hsa_circ_97966,RMVar_hsa_circ_265655,RMVar_hsa_circ_161305,RMVar_hsa_circ_93677,RMVar_hsa_circ_332105,RMVar_hsa_circ_334493,RMVar_hsa_circ_96621,RMVar_hsa_circ_161306,RMVar_hsa_circ_161307 35447 RMVar_ID_35447 Human_SNP_ID_518894860 A-to-I Human chr12 - 123322833 123322833 123322833 CTCCGTCACCCAGGCTGGAGTGCAGTGGTACCATCTTGGCTCACTGCAACCTCTGCCTCCTGGGT CTCCGTCACCCAGGCTGGAGTGCAGTGGTACCTTCTTGGCTCACTGCAACCTCTGCCTCCTGGGT T A SBNO1 Ensembl:ENSG00000139697 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1349140947 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17561570 RMVar_hsa_circ_7345,RMVar_hsa_circ_57531,RMVar_hsa_circ_161302,RMVar_hsa_circ_97966,RMVar_hsa_circ_93677,RMVar_hsa_circ_161307,RMVar_hsa_circ_299588,RMVar_hsa_circ_5136,RMVar_hsa_circ_9389,RMVar_hsa_circ_41035,RMVar_hsa_circ_161310,RMVar_hsa_circ_359431,RMVar_hsa_circ_283557,RMVar_hsa_circ_31067,RMVar_hsa_circ_161317,RMVar_hsa_circ_33401,RMVar_hsa_circ_161318,RMVar_hsa_circ_280061,RMVar_hsa_circ_25956,RMVar_hsa_circ_92146,RMVar_hsa_circ_161320,RMVar_hsa_circ_161319,RMVar_hsa_circ_41868,RMVar_hsa_circ_35797,RMVar_hsa_circ_7822,RMVar_hsa_circ_5176,RMVar_hsa_circ_58739,RMVar_hsa_circ_341880,RMVar_hsa_circ_73010,RMVar_hsa_circ_29140,RMVar_hsa_circ_74941,RMVar_hsa_circ_161326,RMVar_hsa_circ_40988,RMVar_hsa_circ_268504,RMVar_hsa_circ_73418,RMVar_hsa_circ_284847 35448 RMVar_ID_35448 Human_SNP_ID_518900348 A-to-I Human chr12 - 123341266 123341266 123341266 TTCTGTATTTTTAGTAGAGATGCGGTTTCACAATCTTGGCCAGGCTGGTCTTGAACTCCTGACCT TTCTGTATTTTTAGTAGAGATGCGGTTTCACAGTCTTGGCCAGGCTGGTCTTGAACTCCTGACCT T C SBNO1 Ensembl:ENSG00000139697 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs531530647 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7345,RMVar_hsa_circ_93677,RMVar_hsa_circ_161307,RMVar_hsa_circ_9389,RMVar_hsa_circ_161318,RMVar_hsa_circ_92146,RMVar_hsa_circ_7975,RMVar_hsa_circ_2491,RMVar_hsa_circ_2043,RMVar_hsa_circ_5176,RMVar_hsa_circ_161330,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_4343,RMVar_hsa_circ_13440,RMVar_hsa_circ_42297,RMVar_hsa_circ_23895,RMVar_hsa_circ_65931,RMVar_hsa_circ_293777,RMVar_hsa_circ_295963,RMVar_hsa_circ_161339,RMVar_hsa_circ_56723,RMVar_hsa_circ_161340,RMVar_hsa_circ_304795,RMVar_hsa_circ_328651,RMVar_hsa_circ_353542,RMVar_hsa_circ_293021,RMVar_hsa_circ_161341,RMVar_hsa_circ_161342 35449 RMVar_ID_35449 Human_SNP_ID_518900368 A-to-I Human chr12 - 123341327 123341327 123341327 TCTCTGCCTCAGTCTCCCGAGTAGCTGGGATTACAGGTGCCCGCCACCACGCCCAGCTTGTTTCT TCTCTGCCTCAGTCTCCCGAGTAGCTGGGATTGCAGGTGCCCGCCACCACGCCCAGCTTGTTTCT T C SBNO1 Ensembl:ENSG00000139697 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs965671634 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7345,RMVar_hsa_circ_93677,RMVar_hsa_circ_161307,RMVar_hsa_circ_9389,RMVar_hsa_circ_161318,RMVar_hsa_circ_92146,RMVar_hsa_circ_7975,RMVar_hsa_circ_2491,RMVar_hsa_circ_2043,RMVar_hsa_circ_5176,RMVar_hsa_circ_161330,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_4343,RMVar_hsa_circ_13440,RMVar_hsa_circ_42297,RMVar_hsa_circ_23895,RMVar_hsa_circ_65931,RMVar_hsa_circ_293777,RMVar_hsa_circ_295963,RMVar_hsa_circ_161339,RMVar_hsa_circ_56723,RMVar_hsa_circ_161340,RMVar_hsa_circ_304795,RMVar_hsa_circ_328651,RMVar_hsa_circ_353542,RMVar_hsa_circ_293021,RMVar_hsa_circ_161341,RMVar_hsa_circ_161342 35450 RMVar_ID_35450 Human_SNP_ID_518900369 A-to-I Human chr12 - 123341327 123341327 123341327 TCTCTGCCTCAGTCTCCCGAGTAGCTGGGATTACAGGTGCCCGCCACCACGCCCAGCTTGTTTCT TCTCTGCCTCAGTCTCCCGAGTAGCTGGGATTCCAGGTGCCCGCCACCACGCCCAGCTTGTTTCT T G SBNO1 Ensembl:ENSG00000139697 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs965671634 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7345,RMVar_hsa_circ_93677,RMVar_hsa_circ_161307,RMVar_hsa_circ_9389,RMVar_hsa_circ_161318,RMVar_hsa_circ_92146,RMVar_hsa_circ_7975,RMVar_hsa_circ_2491,RMVar_hsa_circ_2043,RMVar_hsa_circ_5176,RMVar_hsa_circ_161330,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_4343,RMVar_hsa_circ_13440,RMVar_hsa_circ_42297,RMVar_hsa_circ_23895,RMVar_hsa_circ_65931,RMVar_hsa_circ_293777,RMVar_hsa_circ_295963,RMVar_hsa_circ_161339,RMVar_hsa_circ_56723,RMVar_hsa_circ_161340,RMVar_hsa_circ_304795,RMVar_hsa_circ_328651,RMVar_hsa_circ_353542,RMVar_hsa_circ_293021,RMVar_hsa_circ_161341,RMVar_hsa_circ_161342 35451 RMVar_ID_35451 Human_SNP_ID_518900881 A-to-I Human chr12 - 123343194 123343194 123343194 AAGTCTCATTCCATCGCCCAGGCTGGAGTGCAATGGCGCGACCTCGGCTTCCTGCAACCCCTGCC AAGTCTCATTCCATCGCCCAGGCTGGAGTGCAGTGGCGCGACCTCGGCTTCCTGCAACCCCTGCC T C SBNO1 Ensembl:ENSG00000139697 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs960883766 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7345,RMVar_hsa_circ_93677,RMVar_hsa_circ_161307,RMVar_hsa_circ_9389,RMVar_hsa_circ_161318,RMVar_hsa_circ_92146,RMVar_hsa_circ_7975,RMVar_hsa_circ_2491,RMVar_hsa_circ_2043,RMVar_hsa_circ_5176,RMVar_hsa_circ_161330,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_4343,RMVar_hsa_circ_13440,RMVar_hsa_circ_42297,RMVar_hsa_circ_23895,RMVar_hsa_circ_65931,RMVar_hsa_circ_293777,RMVar_hsa_circ_295963,RMVar_hsa_circ_161339,RMVar_hsa_circ_56723,RMVar_hsa_circ_161340,RMVar_hsa_circ_304795,RMVar_hsa_circ_328651,RMVar_hsa_circ_353542,RMVar_hsa_circ_293021,RMVar_hsa_circ_161341,RMVar_hsa_circ_161342 35452 RMVar_ID_35452 Human_SNP_ID_518901943 A-to-I Human chr12 - 123346881 123346881 123346881 TAGAGACAGGGTTTTACCATGTTGGCCATGCTAGTCTTGAGCTCCTGACCTCAGGTAATGTGCCC TAGAGACAGGGTTTTACCATGTTGGCCATGCTGGTCTTGAGCTCCTGACCTCAGGTAATGTGCCC T C SBNO1 Ensembl:ENSG00000139697 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1284662628 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7345,RMVar_hsa_circ_9389,RMVar_hsa_circ_7975,RMVar_hsa_circ_2043,RMVar_hsa_circ_5176,RMVar_hsa_circ_161330,RMVar_hsa_circ_161332,RMVar_hsa_circ_80624,RMVar_hsa_circ_37146,RMVar_hsa_circ_77087,RMVar_hsa_circ_161333,RMVar_hsa_circ_4343,RMVar_hsa_circ_42297,RMVar_hsa_circ_23895,RMVar_hsa_circ_293777,RMVar_hsa_circ_295963,RMVar_hsa_circ_161339,RMVar_hsa_circ_161340,RMVar_hsa_circ_304795,RMVar_hsa_circ_293021,RMVar_hsa_circ_161342,RMVar_hsa_circ_363302,RMVar_hsa_circ_161343,RMVar_hsa_circ_282944 35453 RMVar_ID_35453 Human_SNP_ID_518901944 A-to-I Human chr12 - 123346881 123346881 123346881 TAGAGACAGGGTTTTACCATGTTGGCCATGCTAGTCTTGAGCTCCTGACCTCAGGTAATGTGCCC TAGAGACAGGGTTTTACCATGTTGGCCATGCTCGTCTTGAGCTCCTGACCTCAGGTAATGTGCCC T G SBNO1 Ensembl:ENSG00000139697 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1284662628 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7345,RMVar_hsa_circ_9389,RMVar_hsa_circ_7975,RMVar_hsa_circ_2043,RMVar_hsa_circ_5176,RMVar_hsa_circ_161330,RMVar_hsa_circ_161332,RMVar_hsa_circ_80624,RMVar_hsa_circ_37146,RMVar_hsa_circ_77087,RMVar_hsa_circ_161333,RMVar_hsa_circ_4343,RMVar_hsa_circ_42297,RMVar_hsa_circ_23895,RMVar_hsa_circ_293777,RMVar_hsa_circ_295963,RMVar_hsa_circ_161339,RMVar_hsa_circ_161340,RMVar_hsa_circ_304795,RMVar_hsa_circ_293021,RMVar_hsa_circ_161342,RMVar_hsa_circ_363302,RMVar_hsa_circ_161343,RMVar_hsa_circ_282944 35454 RMVar_ID_35454 Human_SNP_ID_518902950 A-to-I Human chr12 - 123350071 123350071 123350071 TTTTTGTCTTTTTTGTAGAGACAGGGTTTGCCATGTTGCCCAGGCTGGTCTTGAACTCCTGAGCT TTTTTGTCTTTTTTGTAGAGACAGGGTTTGCCGTGTTGCCCAGGCTGGTCTTGAACTCCTGAGCT T C SBNO1 Ensembl:ENSG00000139697 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1054124956 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7345,RMVar_hsa_circ_9389,RMVar_hsa_circ_161332,RMVar_hsa_circ_80624,RMVar_hsa_circ_77087,RMVar_hsa_circ_161333,RMVar_hsa_circ_4343,RMVar_hsa_circ_42297,RMVar_hsa_circ_23895,RMVar_hsa_circ_293777,RMVar_hsa_circ_161340,RMVar_hsa_circ_304795,RMVar_hsa_circ_293021,RMVar_hsa_circ_161342,RMVar_hsa_circ_161343,RMVar_hsa_circ_282944,RMVar_hsa_circ_161344,RMVar_hsa_circ_287604 35455 RMVar_ID_35455 Human_SNP_ID_518903794 A-to-I Human chr12 - 123353025 123353025 123353025 GGGAAGCCGAGGCGGACGGATTGCCTGAGCCCAGGAGTTTGAGACCAGCCTGGGCAATACGGTGA GGGAAGCCGAGGCGGACGGATTGCCTGAGCCCGGGAGTTTGAGACCAGCCTGGGCAATACGGTGA T C SBNO1 Ensembl:ENSG00000139697 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1210941713 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80624,RMVar_hsa_circ_161333 35456 RMVar_ID_35456 Human_SNP_ID_518904528 A-to-I Human chr12 - 123355769 123355769 123355769 GTTTATTTTTCATTTTTTTGGGACAGGGTCTCACTCTGTCACCCAGCCTGGAATGCAGTGCCATG GTTTATTTTTCATTTTTTTGGGACAGGGTCTCTCTCTGTCACCCAGCCTGGAATGCAGTGCCATG T A SBNO1 Ensembl:ENSG00000139697 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917025431 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_753896,Human_RBP_ID_11864772 RMVar_hsa_circ_80624,RMVar_hsa_circ_161333 35457 RMVar_ID_35457 Human_SNP_ID_518905080 A-to-I Human chr12 - 123357673 123357673 123357673 TCGGCTCACTGTAACCTCCACTTTCCGGGTTCAAGCTATTCTCCTGTCTCAGCCTCCCGAGTAGC TCGGCTCACTGTAACCTCCACTTTCCGGGTTCGAGCTATTCTCCTGTCTCAGCCTCCCGAGTAGC T C SBNO1 Ensembl:ENSG00000139697 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1272763618 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5491096 RMVar_hsa_circ_80624,RMVar_hsa_circ_161333 35458 RMVar_ID_35458 Human_SNP_ID_518905648 A-to-I Human chr12 - 123359493 123359493 123359493 TGGAGTGCACGAGTGCGATCTTGGCAACCTCCACCTCCTGGGTTCAAGTGATTCTCCCACCTCAG TGGAGTGCACGAGTGCGATCTTGGCAACCTCCGCCTCCTGGGTTCAAGTGATTCTCCCACCTCAG T C SBNO1 Ensembl:ENSG00000139697 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs980461968 Functional Loss SNV dbSNP153 33..33 33 - - - 35459 RMVar_ID_35459 Human_SNP_ID_518906371 A-to-I Human chr12 - 123361711 123361711 123361711 TTTTTTTTTTTTTTAGACTGTCTTGCTCTGTCACCAGGCTGGAGTGCAGTGGGGTGATCTGAGCT TTTTTTTTTTTTTTAGACTGTCTTGCTCTGTCGCCAGGCTGGAGTGCAGTGGGGTGATCTGAGCT T C SBNO1 Ensembl:ENSG00000139697 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1468404233 Functional Loss SNV dbSNP153 33..33 33 - - - 35460 RMVar_ID_35460 Human_SNP_ID_518913925 A-to-I Human chr12 + 123386430 123386430 123386430 TAGAGACGGGGTTTCGCCATGTTGGCCAGGCTAGTCTTGAACTCCTGACCTCAGGTTATCTGCCC TAGAGACGGGGTTTCGCCATGTTGGCCAGGCTGGTCTTGAACTCCTGACCTCAGGTTATCTGCCC A G KMT5A Ensembl:ENSG00000183955 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs543861282 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24945488 35461 RMVar_ID_35461 Human_SNP_ID_518914080 A-to-I Human chr12 + 123387017 123387017 123387017 TAGCTGGGATTACAGGCATGCGCAACCACGCCAAGCTAATTTTTGTATTTTTAGTAGAGACGGGG TAGCTGGGATTACAGGCATGCGCAACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGG A C KMT5A Ensembl:ENSG00000183955 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1158386155 Functional Loss SNV dbSNP153 33..33 33 - - - 35462 RMVar_ID_35462 Human_SNP_ID_518915743 A-to-I Human chr12 + 123392543 123392543 123392543 AAAATTAGCCTGGCATGGTGGCATGCATCTGTAGTCCCAGCTGCTTGGGAGGCTAAGGCAGGAGG AAAATTAGCCTGGCATGGTGGCATGCATCTGTGGTCCCAGCTGCTTGGGAGGCTAAGGCAGGAGG A G KMT5A Ensembl:ENSG00000183955 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1199819871 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_755798 RMVar_hsa_circ_301969 35463 RMVar_ID_35463 Human_SNP_ID_518919186 A-to-I Human chr12 + 123405284 123405284 123405284 GGTGTGATCTCGGCTCATTGCAACCTCCTCTCAGGCTCAAAGAATTCTCCTCCCTCAGCCTCCAG GGTGTGATCTCGGCTCATTGCAACCTCCTCTCGGGCTCAAAGAATTCTCCTCCCTCAGCCTCCAG A G KMT5A Ensembl:ENSG00000183955 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1471771021 Functional Loss SNV dbSNP153 33..33 33 - - - 35464 RMVar_ID_35464 Human_SNP_ID_518920895 A-to-I Human chr12 - 123410996 123410996 123410996 TAAGTCAGGCACAGTGGCTCACGCATGCCTGTAATCACAGCCCTGTGGGAGGGTGAGGCATGAGG TAAGTCAGGCACAGTGGCTCACGCATGCCTGTCATCACAGCCCTGTGGGAGGGTGAGGCATGAGG T G RILPL2 Ensembl:ENSG00000150977 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1165872376 Functional Loss SNV dbSNP153 33..33 33 - - - 35465 RMVar_ID_35465 Human_SNP_ID_518920902 A-to-I Human chr12 - 123411016 123411015 123411017 AATAAATAAATAAATAAAAATAAGTCAGGCACAGTGGCTCACGCATGCCTGTAATCACAGCCCTG AATAAATAAATAAATAAAAATAAGTCAGGCA__GTGGCTCACGCATGCCTGTAATCACAGCCCTG CTG C RILPL2 Ensembl:ENSG00000150977 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1181935369 Functional Loss DEL dbSNP153 32..33 33 - - - 35466 RMVar_ID_35466 Human_SNP_ID_518921006 A-to-I Human chr12 - 123411244 123411244 123411244 GATCACGAGGTCAGGAGACCAGCCTGGCCAACATGGTGAAACCTCGTCTCTACTAAAAATACAAA GATCACGAGGTCAGGAGACCAGCCTGGCCAACGTGGTGAAACCTCGTCTCTACTAAAAATACAAA T C RILPL2 Ensembl:ENSG00000150977 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1182987954 Functional Loss SNV dbSNP153 33..33 33 - - - 35467 RMVar_ID_35467 Human_SNP_ID_518921047 A-to-I Human chr12 - 123411379 123411379 123411379 CGCCTGCCTCGCCCTCCCAAAGTGGTGGGATTACAGGGATTACCGTGCCTGGCCAGCAGTCATCT CGCCTGCCTCGCCCTCCCAAAGTGGTGGGATTTCAGGGATTACCGTGCCTGGCCAGCAGTCATCT T A RILPL2 Ensembl:ENSG00000150977 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs892157284 Functional Loss SNV dbSNP153 33..33 33 - - - 35468 RMVar_ID_35468 Human_SNP_ID_518921080 A-to-I Human chr12 - 123411476 123411475 123411477 AGCAATCATCTTTTATTTTATTTATTTGAGACAGAGTCTCGCTCTGTCGCCCAGGCCGGAGTGCA AGCAATCATCTTTTATTTTATTTATTTGAGA__GAGTCTCGCTCTGTCGCCCAGGCCGGAGTGCA CTG C RILPL2 Ensembl:ENSG00000150977 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1566087573 Functional Loss DEL dbSNP153 32..33 33 - - - 35469 RMVar_ID_35469 Human_SNP_ID_518921303 A-to-I Human chr12 - 123412323 123412323 123412323 CAGCCTAGGCAACATAGTAAGAACCTATCTTTACAAAAAACAAAAAATTAGCCAGGCATGGTGGT CAGCCTAGGCAACATAGTAAGAACCTATCTTTTCAAAAAACAAAAAATTAGCCAGGCATGGTGGT T A RILPL2 Ensembl:ENSG00000150977 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs537651957 Functional Loss SNV dbSNP153 33..33 33 - - - 35470 RMVar_ID_35470 Human_SNP_ID_518922202 A-to-I Human chr12 - 123414871 123414871 123414871 TCTGGAGTGCAGTGGCACGATCTCGGCTCACTACAAGCTCTGCTGCCTACGTTCACGCCATTCTC TCTGGAGTGCAGTGGCACGATCTCGGCTCACTGCAAGCTCTGCTGCCTACGTTCACGCCATTCTC T C RILPL2 Ensembl:ENSG00000150977 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs911137915 Functional Loss SNV dbSNP153 33..33 33 - - - 35471 RMVar_ID_35471 Human_SNP_ID_518922802 A-to-I Human chr12 - 123417151 123417151 123417151 GGGACCACAGGTGTTCACCATCATGCCCAGCTAATTTTTGTATTTTTGGTAAAGATGGGGTTTCT GGGACCACAGGTGTTCACCATCATGCCCAGCTCATTTTTGTATTTTTGGTAAAGATGGGGTTTCT T G RILPL2 Ensembl:ENSG00000150977 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1381674209 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83077,RMVar_hsa_circ_161346,RMVar_hsa_circ_77932,RMVar_hsa_circ_161347 35472 RMVar_ID_35472 Human_SNP_ID_518923238 A-to-I Human chr12 - 123418899 123418899 123418899 TCCTGGCCAACATGGTGAAACCCCAAGCCTGTAGTCCCAGCTACTCAAGAGGCTGAGGCAAGAGA TCCTGGCCAACATGGTGAAACCCCAAGCCTGTGGTCCCAGCTACTCAAGAGGCTGAGGCAAGAGA T C RILPL2 Ensembl:ENSG00000150977 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1343486141 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83077,RMVar_hsa_circ_161346,RMVar_hsa_circ_77932,RMVar_hsa_circ_161347 35473 RMVar_ID_35473 Human_SNP_ID_518923375 A-to-I Human chr12 - 123419309 123419309 123419309 CTCAGAAATCAAGTCAGTAGGCCGGGCGCAGTAGCTCACACCTGTAATCCCAGCACTTTGGGAGG CTCAGAAATCAAGTCAGTAGGCCGGGCGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGG T C RILPL2 Ensembl:ENSG00000150977 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1325465181 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83077,RMVar_hsa_circ_161346,RMVar_hsa_circ_77932,RMVar_hsa_circ_161347 35474 RMVar_ID_35474 Human_SNP_ID_518935478 A-to-I Human chr12 + 123458987 123458987 123458987 TTTCCCCAGAGACAGGGAGTCGCCCAGGCTGGAGAGCGGTGGCGCGATCTCGGCTCACTGCAGCG TTTCCCCAGAGACAGGGAGTCGCCCAGGCTGGTGAGCGGTGGCGCGATCTCGGCTCACTGCAGCG A T SNRNP35 Ensembl:ENSG00000184209 Protein coding exon GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs754850152 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1439786 35475 RMVar_ID_35475 Human_SNP_ID_518935494 A-to-I Human chr12 + 123459039 123459039 123459039 GCTCACTGCAGCGTCGACATTTCGGGTCAAGCAGTCCTCCCGCCTCAGCCTCTCAAGTATCTGGG GCTCACTGCAGCGTCGACATTTCGGGTCAAGCGGTCCTCCCGCCTCAGCCTCTCAAGTATCTGGG A G SNRNP35 Ensembl:ENSG00000184209 Protein coding exon GSE47997;GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 23474544,24183664,29129909,31158229,31158229 RNA-Seq:(High) rs1312717961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1439786 35476 RMVar_ID_35476 Human_SNP_ID_518935520 A-to-I Human chr12 + 123459124 123459124 123459124 CCCGGAGAATTGATTATTGATTGATTGATTGAAACGGGGTCTCACTTTGTTGCCCAGGCTGGTCT CCCGGAGAATTGATTATTGATTGATTGATTGAGACGGGGTCTCACTTTGTTGCCCAGGCTGGTCT A G SNRNP35 Ensembl:ENSG00000184209 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1391855895 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24945579 35477 RMVar_ID_35477 Human_SNP_ID_518935585 A-to-I Human chr12 + 123459390 123459390 123459390 ATCCTGAAGCTCAAAATTTACTGACCTCAAATAATCCACCCGCCTTGGCCTCCCAAAGTGCTGGG ATCCTGAAGCTCAAAATTTACTGACCTCAAATGATCCACCCGCCTTGGCCTCCCAAAGTGCTGGG A G SNRNP35 Ensembl:ENSG00000184209 Protein coding intron GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-Seq:(High) rs934187914 Functional Loss SNV dbSNP153 33..33 33 - - - 35478 RMVar_ID_35478 Human_SNP_ID_518935587 A-to-I Human chr12 + 123459395 123459395 123459395 GAAGCTCAAAATTTACTGACCTCAAATAATCCACCCGCCTTGGCCTCCCAAAGTGCTGGGATTAC GAAGCTCAAAATTTACTGACCTCAAATAATCCCCCCGCCTTGGCCTCCCAAAGTGCTGGGATTAC A C SNRNP35 Ensembl:ENSG00000184209 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs889903492 Functional Loss SNV dbSNP153 33..33 33 - - - 35479 RMVar_ID_35479 Human_SNP_ID_518935588 A-to-I Human chr12 + 123459395 123459395 123459395 GAAGCTCAAAATTTACTGACCTCAAATAATCCACCCGCCTTGGCCTCCCAAAGTGCTGGGATTAC GAAGCTCAAAATTTACTGACCTCAAATAATCCGCCCGCCTTGGCCTCCCAAAGTGCTGGGATTAC A G SNRNP35 Ensembl:ENSG00000184209 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs889903492 Functional Loss SNV dbSNP153 33..33 33 - - - 35480 RMVar_ID_35480 Human_SNP_ID_518935687 A-to-I Human chr12 + 123459769 123459769 123459769 GAGATTGGCCATTGCACTCCAGCCTGGGTGACAGAGTGAGACTTTGTCTCGAGTAAAAAAAGAGA GAGATTGGCCATTGCACTCCAGCCTGGGTGACGGAGTGAGACTTTGTCTCGAGTAAAAAAAGAGA A G SNRNP35 Ensembl:ENSG00000184209 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1442471212 Functional Loss SNV dbSNP153 33..33 33 - - - 35481 RMVar_ID_35481 Human_SNP_ID_518935863 A-to-I Human chr12 + 123460504 123460503 123460505 GAGGTTAGTACAGGCTGGGTTCGCTGGCTCACATGTGTAATCCCAGCACTTTGGGAGGCTGAGGC GAGGTTAGTACAGGCTGGGTTCGCTGGCTCAC__GTGTAATCCCAGCACTTTGGGAGGCTGAGGC CAT C SNRNP35 Ensembl:ENSG00000184209 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1170277052 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_6148545 RMVar_hsa_circ_161348,RMVar_hsa_circ_126128 35482 RMVar_ID_35482 Human_SNP_ID_518935865 A-to-I Human chr12 + 123460504 123460504 123460504 GAGGTTAGTACAGGCTGGGTTCGCTGGCTCACATGTGTAATCCCAGCACTTTGGGAGGCTGAGGC GAGGTTAGTACAGGCTGGGTTCGCTGGCTCACGTGTGTAATCCCAGCACTTTGGGAGGCTGAGGC A G SNRNP35 Ensembl:ENSG00000184209 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs969710363 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6148545 RMVar_hsa_circ_161348,RMVar_hsa_circ_126128 35483 RMVar_ID_35483 Human_SNP_ID_518935879 A-to-I Human chr12 + 123460575 123460575 123460575 ATAGCTCATGCCCAGGAGTTCAAGATCAGCCTATGCAATATAGTGAGACCCCATCTCTACAAAAA ATAGCTCATGCCCAGGAGTTCAAGATCAGCCTGTGCAATATAGTGAGACCCCATCTCTACAAAAA A G SNRNP35 Ensembl:ENSG00000184209 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs371147762 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_161348,RMVar_hsa_circ_126128 35484 RMVar_ID_35484 Human_SNP_ID_518935927 A-to-I Human chr12 + 123460651 123460651 123460651 AAAAAAGCTGGGTATGGTGGCGCATAGTGAGTAATTCCAGGTACTCAGGAGGCTAGGGTGGGAGA AAAAAAGCTGGGTATGGTGGCGCATAGTGAGTGATTCCAGGTACTCAGGAGGCTAGGGTGGGAGA A G SNRNP35 Ensembl:ENSG00000184209 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs555904342 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_161348,RMVar_hsa_circ_126128 35485 RMVar_ID_35485 Human_SNP_ID_518935945 A-to-I Human chr12 + 123460736 123460736 123460736 GTGCCACTGTACTCCAGTCTGGGCAACAGAGCAAGACCCTGTCTCAAAAAAAATTCAAGCGATTC GTGCCACTGTACTCCAGTCTGGGCAACAGAGCGAGACCCTGTCTCAAAAAAAATTCAAGCGATTC A G SNRNP35 Ensembl:ENSG00000184209 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1321966237 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_161348,RMVar_hsa_circ_126128 35486 RMVar_ID_35486 Human_SNP_ID_518936289 A-to-I Human chr12 + 123461902 123461902 123461902 CGCCACCACACCCAGCTAATTTTTGTATGTTTAGTAGAGATGGGGTTTCGCTATGTTGCTGAGGC CGCCACCACACCCAGCTAATTTTTGTATGTTTCGTAGAGATGGGGTTTCGCTATGTTGCTGAGGC A C SNRNP35 Ensembl:ENSG00000184209 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1464810313 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_161348,RMVar_hsa_circ_126128 35487 RMVar_ID_35487 Human_SNP_ID_518938484 A-to-I Human chr12 - 123470386 123470386 123470386 TCATTGCAGCTATGAACCCCTGGGCTCAAGCAATCCTCCCACCTCAGCCTCCCAAGTAGCTGGTA TCATTGCAGCTATGAACCCCTGGGCTCAAGCAGTCCTCCCACCTCAGCCTCCCAAGTAGCTGGTA T C RILPL1 Ensembl:ENSG00000188026 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs577824301 Functional Loss SNV dbSNP153 33..33 33 - - - 35488 RMVar_ID_35488 Human_SNP_ID_518939896 A-to-I Human chr12 - 123475977 123475977 123475977 ATCGCTTGAACCCGGGAGGAGGAGGTTGCAGTAAGCTGAGATTGCGCCACCGCACTCCAGCCTGG ATCGCTTGAACCCGGGAGGAGGAGGTTGCAGTGAGCTGAGATTGCGCCACCGCACTCCAGCCTGG T C RILPL1 Ensembl:ENSG00000188026 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1283067561 Functional Loss SNV dbSNP153 33..33 33 - - - 35489 RMVar_ID_35489 Human_SNP_ID_518946594 A-to-I Human chr12 - 123503026 123503026 123503026 AAAATTAGCCGAGCGTGGTGGCGGGGACCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA AAAATTAGCCGAGCGTGGTGGCGGGGACCTGTTGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA T A RILPL1 Ensembl:ENSG00000188026 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1185594670 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_322060,RMVar_hsa_circ_351971 35490 RMVar_ID_35490 Human_SNP_ID_518950788 A-to-I Human chr12 - 123515535 123515535 123515535 TGAGGCAGGAGAATCTCTTGAACCCAGGAGGCAGAGGTCGTAGTGAGTTGAGATCGCGCCACTGC TGAGGCAGGAGAATCTCTTGAACCCAGGAGGCGGAGGTCGTAGTGAGTTGAGATCGCGCCACTGC T C RILPL1 Ensembl:ENSG00000188026 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1316105622 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22710581 RMVar_hsa_circ_322060,RMVar_hsa_circ_351971 35491 RMVar_ID_35491 Human_SNP_ID_518950789 A-to-I Human chr12 - 123515535 123515535 123515535 TGAGGCAGGAGAATCTCTTGAACCCAGGAGGCAGAGGTCGTAGTGAGTTGAGATCGCGCCACTGC TGAGGCAGGAGAATCTCTTGAACCCAGGAGGCCGAGGTCGTAGTGAGTTGAGATCGCGCCACTGC T G RILPL1 Ensembl:ENSG00000188026 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1316105622 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22710581 RMVar_hsa_circ_322060,RMVar_hsa_circ_351971 35492 RMVar_ID_35492 Human_SNP_ID_518951168 A-to-I Human chr12 - 123517005 123517005 123517005 GGAGTGCAGTGGTGCGATCTTGGCTCACTGCAACCTCCTCCTCCCTCACCTCCTGCTCAGGTAAT GGAGTGCAGTGGTGCGATCTTGGCTCACTGCAGCCTCCTCCTCCCTCACCTCCTGCTCAGGTAAT T C RILPL1 Ensembl:ENSG00000188026 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041777861 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_322060,RMVar_hsa_circ_351971 35493 RMVar_ID_35493 Human_SNP_ID_518951329 A-to-I Human chr12 - 123517610 123517610 123517610 TGAGACCAGCCTGGGCAACATGGCAAAGCCCCATCTCTACAAAAAATACAATAAGTAGCCAGGTG TGAGACCAGCCTGGGCAACATGGCAAAGCCCCGTCTCTACAAAAAATACAATAAGTAGCCAGGTG T C RILPL1 Ensembl:ENSG00000188026 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474834505 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_322060,RMVar_hsa_circ_351971 35494 RMVar_ID_35494 Human_SNP_ID_518951491 A-to-I Human chr12 - 123518339 123518339 123518339 CCACGCCTGGCTAAGTTTTAAATTTTTTTGGTAGAGACGGGGGTCTCACTATGTTGCCCAGGCTG CCACGCCTGGCTAAGTTTTAAATTTTTTTGGTGGAGACGGGGGTCTCACTATGTTGCCCAGGCTG T C RILPL1 Ensembl:ENSG00000188026 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1428197627 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_322060,RMVar_hsa_circ_351971 35495 RMVar_ID_35495 Human_SNP_ID_518951511 A-to-I Human chr12 - 123518395 123518395 123518395 TCAAAAGATTCTCCCACCTCAGTCTTCTAAGTAGCTGGGATGACAGGTGTGCACCACCACGCCTG TCAAAAGATTCTCCCACCTCAGTCTTCTAAGTGGCTGGGATGACAGGTGTGCACCACCACGCCTG T C RILPL1 Ensembl:ENSG00000188026 Protein coding intron GSE47997;GSE100210;GSE99789;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BERP35T4 cell line - 23474544,29129909,29796672,31158229 RNA-Seq:(High) rs1215718541 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_322060,RMVar_hsa_circ_351971 35496 RMVar_ID_35496 Human_SNP_ID_518951513 A-to-I Human chr12 - 123518399 123518399 123518399 AGGCTCAAAAGATTCTCCCACCTCAGTCTTCTAAGTAGCTGGGATGACAGGTGTGCACCACCACG AGGCTCAAAAGATTCTCCCACCTCAGTCTTCTGAGTAGCTGGGATGACAGGTGTGCACCACCACG T C RILPL1 Ensembl:ENSG00000188026 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1488959341 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24945715 RMVar_hsa_circ_322060,RMVar_hsa_circ_351971 35497 RMVar_ID_35497 Human_SNP_ID_518951529 A-to-I Human chr12 - 123518431 123518431 123518431 GCAATTATAGTTCACCATAGCCTCAACCTCCCAGGCTCAAAAGATTCTCCCACCTCAGTCTTCTA GCAATTATAGTTCACCATAGCCTCAACCTCCCGGGCTCAAAAGATTCTCCCACCTCAGTCTTCTA T C RILPL1 Ensembl:ENSG00000188026 Protein coding intron GSE100210;GSE99789;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BERP35T1 cell line - 29129909,29796672,31158229 RNA-Seq:(High) rs1363058817 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_322060,RMVar_hsa_circ_351971 35498 RMVar_ID_35498 Human_SNP_ID_518951651 A-to-I Human chr12 - 123518869 123518869 123518869 TATTTTTAGCGGAGACGGGATTTCACCGTGTTAGCCAGTATGGTCTCGATCTCCTGACCTCATGA TATTTTTAGCGGAGACGGGATTTCACCGTGTTGGCCAGTATGGTCTCGATCTCCTGACCTCATGA T C RILPL1 Ensembl:ENSG00000188026 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1311917417 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_351971 35499 RMVar_ID_35499 Human_SNP_ID_518952033 A-to-I Human chr12 - 123520367 123520367 123520367 TTTAATAGAGACGGGATTTCACCATGTTGGCCAGGCTGGCCTTGAAGTTCTGACCTAAGGTGATC TTTAATAGAGACGGGATTTCACCATGTTGGCCCGGCTGGCCTTGAAGTTCTGACCTAAGGTGATC T G RILPL1 Ensembl:ENSG00000188026 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1165046527 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_351971 35500 RMVar_ID_35500 Human_SNP_ID_518952071 A-to-I Human chr12 - 123520526 123520526 123520526 GAGACGGAGTCTCACTCCGTCGACCAGGCTGTAATGCAGTGGCGCAATCTTGGCTCACTGCAACC GAGACGGAGTCTCACTCCGTCGACCAGGCTGTGATGCAGTGGCGCAATCTTGGCTCACTGCAACC T C RILPL1 Ensembl:ENSG00000188026 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956229004 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_351971 35501 RMVar_ID_35501 Human_SNP_ID_518952752 A-to-I Human chr12 - 123521808 123521808 123521808 AGATCGCAGCACTGCACTCCAGCCTGGGCGACAGAGCAAGACTATGTCTCAAAAAAAAAAGTATA AGATCGCAGCACTGCACTCCAGCCTGGGCGACGGAGCAAGACTATGTCTCAAAAAAAAAAGTATA T C RILPL1 Ensembl:ENSG00000188026 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1297097718 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_351971 35502 RMVar_ID_35502 Human_SNP_ID_518952775 A-to-I Human chr12 - 123521897 123521897 123521897 GGAGGCGGGCGCCTGTAGAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGATTCGCTTGAACCCA GGAGGCGGGCGCCTGTAGAGTCCCAGCTACTCTGGAGGCTGAGGCAGGAGATTCGCTTGAACCCA T A RILPL1 Ensembl:ENSG00000188026 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs916539380 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_351971 35503 RMVar_ID_35503 Human_SNP_ID_518953533 A-to-I Human chr12 - 123524914 123524914 123524914 TTGGCCAGGCTGGTCATGGACTTCTGACCTCAAGTGATCCGCCTGCCTTGGCCTCCCAAGTGCTG TTGGCCAGGCTGGTCATGGACTTCTGACCTCAGGTGATCCGCCTGCCTTGGCCTCCCAAGTGCTG T C RILPL1 Ensembl:ENSG00000188026 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs988524561 Functional Loss SNV dbSNP153 33..33 33 - - - 35504 RMVar_ID_35504 Human_SNP_ID_518953555 A-to-I Human chr12 - 123525045 123525045 123525045 TCACTGCAAACTCCGCTTCCCAGCTTCAAGTAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGA TCACTGCAAACTCCGCTTCCCAGCTTCAAGTAGTTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGA T C RILPL1 Ensembl:ENSG00000188026 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs938609855 Functional Loss SNV dbSNP153 33..33 33 - - - 35505 RMVar_ID_35505 Human_SNP_ID_518953577 A-to-I Human chr12 - 123525124 123525122 123525124 TTTATTTATTATTATTATTTTTTCCAAGACAGAGTCTCACTCTGTCACCCAGGCTGGAGTGCAGT TTTATTTATTATTATTATTTTTTCCAAGACAG__TCTCACTCTGTCACCCAGGCTGGAGTGCAGT ACT A RILPL1 Ensembl:ENSG00000188026 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1299530289 Functional Loss DEL dbSNP153 33..34 33 - - - 35506 RMVar_ID_35506 Human_SNP_ID_518953580 A-to-I Human chr12 - 123525124 123525124 123525124 TTTATTTATTATTATTATTTTTTCCAAGACAGAGTCTCACTCTGTCACCCAGGCTGGAGTGCAGT TTTATTTATTATTATTATTTTTTCCAAGACAGTGTCTCACTCTGTCACCCAGGCTGGAGTGCAGT T A RILPL1 Ensembl:ENSG00000188026 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444611847 Functional Loss SNV dbSNP153 33..33 33 - - - 35507 RMVar_ID_35507 Human_SNP_ID_518953774 A-to-I Human chr12 - 123525744 123525743 123525745 GCCCTGGAGGTTGAGACAAGCCTGGGCAACATAGCAATACCCCATTTGTTTCTTTTTTTTTTTTT GCCCTGGAGGTTGAGACAAGCCTGGGCAACA__GCAATACCCCATTTGTTTCTTTTTTTTTTTTT CTA C RILPL1 Ensembl:ENSG00000188026 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1344570980 Functional Loss DEL dbSNP153 32..33 33 - - - 35508 RMVar_ID_35508 Human_SNP_ID_518954226 A-to-I Human chr12 - 123527619 123527619 123527619 TCAGTCTGTCACCCAGGCTGGAGTGCAGTGGCATGATCTCGGCTCACTGCAACCTCTGCTTCCCT TCAGTCTGTCACCCAGGCTGGAGTGCAGTGGCGTGATCTCGGCTCACTGCAACCTCTGCTTCCCT T C RILPL1 Ensembl:ENSG00000188026 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1336138176 Functional Loss SNV dbSNP153 33..33 33 - - - 35509 RMVar_ID_35509 Human_SNP_ID_518954399 A-to-I Human chr12 - 123528345 123528341 123528345 TTATCTTTTTTTTTTTTTTGAGACAGCATCTCACTCTGTTGCCCAGGCTGGCGTGCCGTGCGTGA TTATCTTTTTTTTTTTTTTGAGACAGCATCTC____TGTTGCCCAGGCTGGCGTGCCGTGCGTGA AGAGT A RILPL1 Ensembl:ENSG00000188026 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1198183333 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_17561327 35510 RMVar_ID_35510 Human_SNP_ID_518954690 A-to-I Human chr12 - 123529339 123529339 123529339 TGCGTTGAGCCGAGATCATATCACTGCACTCCAGCCTGAGCAACAGAGCGAGACTTTGTCTCAGA TGCGTTGAGCCGAGATCATATCACTGCACTCCGGCCTGAGCAACAGAGCGAGACTTTGTCTCAGA T C RILPL1 Ensembl:ENSG00000188026 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs962279526 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18511074 35511 RMVar_ID_35511 Human_SNP_ID_518954834 A-to-I Human chr12 - 123529835 123529835 123529835 GGGACGTACTCTGTCATCCAGGCCAGAGAGCAATGATGGCATCACGGCTCCCTGCAGCCCTGAAC GGGACGTACTCTGTCATCCAGGCCAGAGAGCAGTGATGGCATCACGGCTCCCTGCAGCCCTGAAC T C RILPL1 Ensembl:ENSG00000188026 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs201855082 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12076723 35512 RMVar_ID_35512 Human_SNP_ID_518954840 A-to-I Human chr12 - 123529843 123529843 123529843 TTGAGTCAGGGACGTACTCTGTCATCCAGGCCAGAGAGCAATGATGGCATCACGGCTCCCTGCAG TTGAGTCAGGGACGTACTCTGTCATCCAGGCCGGAGAGCAATGATGGCATCACGGCTCCCTGCAG T C RILPL1 Ensembl:ENSG00000188026 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs540799117 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12076723 35513 RMVar_ID_35513 Human_SNP_ID_518954976 A-to-I Human chr12 - 123530262 123530262 123530262 ATTCAGGAAGCTGAGGCAGGAGAATCGCTTGAACCCGGGAGGCAGAGATTGCAGCGAGTCGAAAT ATTCAGGAAGCTGAGGCAGGAGAATCGCTTGATCCCGGGAGGCAGAGATTGCAGCGAGTCGAAAT T A RILPL1 Ensembl:ENSG00000188026 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1003029568 Functional Loss SNV dbSNP153 33..33 33 - - - 35514 RMVar_ID_35514 Human_SNP_ID_518954977 A-to-I Human chr12 - 123530263 123530263 123530263 TATTCAGGAAGCTGAGGCAGGAGAATCGCTTGAACCCGGGAGGCAGAGATTGCAGCGAGTCGAAA TATTCAGGAAGCTGAGGCAGGAGAATCGCTTGCACCCGGGAGGCAGAGATTGCAGCGAGTCGAAA T G RILPL1 Ensembl:ENSG00000188026 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1434415193 Functional Loss SNV dbSNP153 33..33 33 - - - 35515 RMVar_ID_35515 Human_SNP_ID_518955027 A-to-I Human chr12 - 123530434 123530434 123530434 GGCTGGGCGCGGTGGCTCACACCTGTAATCCCAGCACTTTTGGGGGGCCAAGGCGGGTGGATCAC GGCTGGGCGCGGTGGCTCACACCTGTAATCCCGGCACTTTTGGGGGGCCAAGGCGGGTGGATCAC T C RILPL1 Ensembl:ENSG00000188026 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs552699940 Functional Loss SNV dbSNP153 33..33 33 - - - 35516 RMVar_ID_35516 Human_SNP_ID_518970870 A-to-I Human chr12 + 123590861 123590861 123590861 AAAAAATTAGCTGGGTGTGGTGGCGTGCACCTATAGTCCCAGCTACTCGGGAGGCTGAGGCATGA AAAAAATTAGCTGGGTGTGGTGGCGTGCACCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCATGA A G TMED2 Ensembl:ENSG00000086598 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1206302372 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106433,RMVar_hsa_circ_124313,RMVar_hsa_circ_161352,RMVar_hsa_circ_161354,RMVar_hsa_circ_161356,RMVar_hsa_circ_98990 35517 RMVar_ID_35517 Human_SNP_ID_518971359 A-to-I Human chr12 + 123593189 123593189 123593189 GGCTTGAGTGATCCACCTGCCTCTGCCTTTCAAAGTGCTGGGATTACAGGCCTGAGCCACTGTGT GGCTTGAGTGATCCACCTGCCTCTGCCTTTCAGAGTGCTGGGATTACAGGCCTGAGCCACTGTGT A G TMED2 Ensembl:ENSG00000086598 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs540591938 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106433,RMVar_hsa_circ_124313,RMVar_hsa_circ_161352,RMVar_hsa_circ_161354,RMVar_hsa_circ_161356,RMVar_hsa_circ_98990 35518 RMVar_ID_35518 Human_SNP_ID_518971575 A-to-I Human chr12 + 123594008 123594008 123594008 TTTTTGGTATTGTAGAGACTGGGTTTCTCCATATTGCCCAGGGTTGGCCTCTGACTCCTGAGCAA TTTTTGGTATTGTAGAGACTGGGTTTCTCCATGTTGCCCAGGGTTGGCCTCTGACTCCTGAGCAA A G TMED2 Ensembl:ENSG00000086598 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1418611522 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6148733 RMVar_hsa_circ_106433,RMVar_hsa_circ_124313,RMVar_hsa_circ_161352,RMVar_hsa_circ_161354,RMVar_hsa_circ_161356,RMVar_hsa_circ_98990 35519 RMVar_ID_35519 Human_SNP_ID_518971707 A-to-I Human chr12 + 123594502 123594502 123594502 CTGGAGAGTTGGACACAATGGCTTGTGCCTGTAGTCTTAGCTGCTTCTGAGCCTGAGGCAGGAGG CTGGAGAGTTGGACACAATGGCTTGTGCCTGTGGTCTTAGCTGCTTCTGAGCCTGAGGCAGGAGG A G TMED2 Ensembl:ENSG00000086598 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1355203202 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106433,RMVar_hsa_circ_124313,RMVar_hsa_circ_161352,RMVar_hsa_circ_161354,RMVar_hsa_circ_161356,RMVar_hsa_circ_98990 35520 RMVar_ID_35520 Human_SNP_ID_518974051 A-to-I Human chr12 + 123603592 123603592 123603592 TTTTGTATTTTTAGTAGATACGGGGTTTCACCATCTCGGCCAGGTTGGTCTTGAACTCCTGACCT TTTTGTATTTTTAGTAGATACGGGGTTTCACCGTCTCGGCCAGGTTGGTCTTGAACTCCTGACCT A G DDX55 Ensembl:ENSG00000111364 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs974583358 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11866460,Human_RBP_ID_22900464 RMVar_hsa_circ_94631,RMVar_hsa_circ_161359 35521 RMVar_ID_35521 Human_SNP_ID_518974154 A-to-I Human chr12 + 123603902 123603902 123603902 TCGGCTCACTGCAACTTCTGCCTCCCGGGTTCAAGCTATTCTCCCATCTCAGCCTTCCAAGTAGC TCGGCTCACTGCAACTTCTGCCTCCCGGGTTCCAGCTATTCTCCCATCTCAGCCTTCCAAGTAGC A C DDX55 Ensembl:ENSG00000111364 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1487424263 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11866475 RMVar_hsa_circ_94631,RMVar_hsa_circ_161359 35522 RMVar_ID_35522 Human_SNP_ID_518974737 A-to-I Human chr12 + 123606251 123606251 123606251 AGAAGCTGGCTACAAATGTGAAAAAATAGGCCAGAAGCCGTGGCTCACGCCTGTAATCCCAGCAC AGAAGCTGGCTACAAATGTGAAAAAATAGGCCGGAAGCCGTGGCTCACGCCTGTAATCCCAGCAC A G DDX55 Ensembl:ENSG00000111364 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1424587313 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5347010 RMVar_hsa_circ_6666,RMVar_hsa_circ_94631,RMVar_hsa_circ_161359,RMVar_hsa_circ_341460,RMVar_hsa_circ_365330,RMVar_hsa_circ_378373,RMVar_hsa_circ_333231,RMVar_hsa_circ_87842,RMVar_hsa_circ_24028,RMVar_hsa_circ_161362,RMVar_hsa_circ_65333,RMVar_hsa_circ_161363 35523 RMVar_ID_35523 Human_SNP_ID_518977465 A-to-I Human chr12 + 123617056 123617056 123617056 CCTGTAGTCCCAGCTACTTGAGAGGCTGAGGCAGGAGAATCGCTTGAGCGCAGGAGGCAGAGGTG CCTGTAGTCCCAGCTACTTGAGAGGCTGAGGCGGGAGAATCGCTTGAGCGCAGGAGGCAGAGGTG A G DDX55 Ensembl:ENSG00000111364 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1173359892 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2311078,Human_RBP_ID_11866966 RMVar_hsa_circ_6666,RMVar_hsa_circ_87842,RMVar_hsa_circ_161362,RMVar_hsa_circ_92983,RMVar_hsa_circ_161364,RMVar_hsa_circ_368404,RMVar_hsa_circ_107907,RMVar_hsa_circ_288362,RMVar_hsa_circ_161369,RMVar_hsa_circ_303829,RMVar_hsa_circ_276373,RMVar_hsa_circ_161371,RMVar_hsa_circ_161372,RMVar_hsa_circ_161370 35524 RMVar_ID_35524 Human_SNP_ID_518979413 A-to-I Human chr12 - 123622937 123622934 123622937 TTTTTAATTGTTCCTTTATTGTAATTGAGACGAGGTCTCACCGTGTTGCCTAGGCTGGTCCCAAA TTTTTAATTGTTCCTTTATTGTAATTGAGACG___TCTCACCGTGTTGCCTAGGCTGGTCCCAAA ACCT A EIF2B1 Ensembl:ENSG00000111361 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs958266139 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_11867091 RMVar_hsa_circ_115197,RMVar_hsa_circ_161375 35525 RMVar_ID_35525 Human_SNP_ID_518979479 A-to-I Human chr12 - 123623137 123623137 123623137 ACCTCAGGTGATCCACCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCACAT ACCTCAGGTGATCCACCCACCTCGGCCTCCCAGAGTGCTGGGATTACAGGCGTGAGCCACCACAT T C EIF2B1 Ensembl:ENSG00000111361 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs569850861 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115197,RMVar_hsa_circ_161375 35526 RMVar_ID_35526 Human_SNP_ID_518979536 A-to-I Human chr12 - 123623277 123623277 123623277 GGTTCAAGCGAGTCTCCTGCTTCAGCCTCCCTAGTAGCTGGGATTACAGGCACCCCCCATCCCAC GGTTCAAGCGAGTCTCCTGCTTCAGCCTCCCTGGTAGCTGGGATTACAGGCACCCCCCATCCCAC T C EIF2B1 Ensembl:ENSG00000111361 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs903687614 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24946156 RMVar_hsa_circ_115197,RMVar_hsa_circ_161375 35527 RMVar_ID_35527 Human_SNP_ID_518979726 A-to-I Human chr12 - 123623915 123623915 123623915 TTTCCACTTCCCAAAGTGCTAGGATTACAGGCATGAGCCACTGTGGCCGGCCTGTCATTTGTTTT TTTCCACTTCCCAAAGTGCTAGGATTACAGGCGTGAGCCACTGTGGCCGGCCTGTCATTTGTTTT T C EIF2B1 Ensembl:ENSG00000111361 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1318560059 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17062430 RMVar_hsa_circ_115197,RMVar_hsa_circ_161375 35528 RMVar_ID_35528 Human_SNP_ID_518979874 A-to-I Human chr12 - 123624361 123624361 123624361 CCAGCTGCCCAGGAAGCTGAGGCAGGAGTATCACGTGAGCCCAGGAATTTGAGGTTGCAGTAAGT CCAGCTGCCCAGGAAGCTGAGGCAGGAGTATCGCGTGAGCCCAGGAATTTGAGGTTGCAGTAAGT T C EIF2B1 Ensembl:ENSG00000111361 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs539363937 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17561575 RMVar_hsa_circ_115197,RMVar_hsa_circ_161375 35529 RMVar_ID_35529 Human_SNP_ID_518979880 A-to-I Human chr12 - 123624383 123624383 123624383 GTGGTGGTGCTTGCCTGTAGTTCCAGCTGCCCAGGAAGCTGAGGCAGGAGTATCACGTGAGCCCA GTGGTGGTGCTTGCCTGTAGTTCCAGCTGCCCGGGAAGCTGAGGCAGGAGTATCACGTGAGCCCA T C EIF2B1 Ensembl:ENSG00000111361 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569866461 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17561575 RMVar_hsa_circ_115197,RMVar_hsa_circ_161375 35530 RMVar_ID_35530 Human_SNP_ID_518980972 A-to-I Human chr12 - 123628645 123628645 123628645 AAAGAGGTTATGGAGGCTGGGCATGGTGGCTCATGCCTGTAATCCCAGCACTTTGGAAAGCCAAG AAAGAGGTTATGGAGGCTGGGCATGGTGGCTCGTGCCTGTAATCCCAGCACTTTGGAAAGCCAAG T C EIF2B1 Ensembl:ENSG00000111361 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1304037110 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38129,RMVar_hsa_circ_115197,RMVar_hsa_circ_161375,RMVar_hsa_circ_306871,RMVar_hsa_circ_348531,RMVar_hsa_circ_105703,RMVar_hsa_circ_161377,RMVar_hsa_circ_161378 35531 RMVar_ID_35531 Human_SNP_ID_518983215 A-to-I Human chr12 + 123636520 123636520 123636520 TCCTAGAGCCGGGCACGGCGGCACATGCCTGTAATCCCAACACTTTAGGAGGCTGAGGTGGGAGG TCCTAGAGCCGGGCACGGCGGCACATGCCTGTGATCCCAACACTTTAGGAGGCTGAGGTGGGAGG A G GTF2H3 Ensembl:ENSG00000111358 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1366528026 Functional Loss SNV dbSNP153 33..33 33 - - - 35532 RMVar_ID_35532 Human_SNP_ID_518986236 A-to-I Human chr12 + 123648129 123648129 123648129 TTGAAGAGATTAAAGATCTAATGACCAAAAGTAACAACTTTTAAACATTGTTATTTTGCAAATAG TTGAAGAGATTAAAGATCTAATGACCAAAAGTGACAACTTTTAAACATTGTTATTTTGCAAATAG A G GTF2H3 Ensembl:ENSG00000111358 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1290484502 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2311128,Human_RBP_ID_17812238 RMVar_hsa_circ_9505,RMVar_hsa_circ_117332,RMVar_hsa_circ_299018,RMVar_hsa_circ_93528,RMVar_hsa_circ_161383,RMVar_hsa_circ_161384,RMVar_hsa_circ_161385,RMVar_hsa_circ_276352,RMVar_hsa_circ_95852,RMVar_hsa_circ_161388,RMVar_hsa_circ_161389,RMVar_hsa_circ_161390,RMVar_hsa_circ_339100,RMVar_hsa_circ_369576,RMVar_hsa_circ_43282 35533 RMVar_ID_35533 Human_SNP_ID_518988572 A-to-I Human chr12 + 123658063 123658053 123658063 GACCAAATTCAAAAGAGTTTTATTTTTATTTTATTTTATTTTATTTTTAGACAGAGTCTTGCTCT GACCAAATTCAAAAGAGTTTTAT__________TTTTATTTTATTTTTAGACAGAGTCTTGCTCT TTTTTATTTTA T GTF2H3 Ensembl:ENSG00000111358 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs918026829 Functional Loss DEL dbSNP153 24..33 33 - - - Human_RBP_ID_6149178 RMVar_hsa_circ_93528,RMVar_hsa_circ_161385,RMVar_hsa_circ_374063,RMVar_hsa_circ_161392 35534 RMVar_ID_35534 Human_SNP_ID_518988573 A-to-I Human chr12 + 123658063 123658053 123658063 GACCAAATTCAAAAGAGTTTTATTTTTATTTTATTTTATTTTATTTTTAGACAGAGTCTTGCTCT GACCAAATTCAAAAGAGTTTTATTTTTA_____TTTTATTTTATTTTTAGACAGAGTCTTGCTCT TTTTTATTTTA TTTTTA GTF2H3 Ensembl:ENSG00000111358 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs918026829 Functional Loss DEL dbSNP153 29..33 33 - - - Human_RBP_ID_6149178 RMVar_hsa_circ_93528,RMVar_hsa_circ_161385,RMVar_hsa_circ_374063,RMVar_hsa_circ_161392 35535 RMVar_ID_35535 Human_SNP_ID_518988641 A-to-I Human chr12 + 123658343 123658343 123658343 GGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGCGGCTGGGATTACAGGTGCCCGCCACTACG GGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCTAGCGGCTGGGATTACAGGTGCCCGCCACTACG A T GTF2H3 Ensembl:ENSG00000111358 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs969492905 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93528,RMVar_hsa_circ_161385,RMVar_hsa_circ_374063,RMVar_hsa_circ_161392 35536 RMVar_ID_35536 Human_SNP_ID_518988656 A-to-I Human chr12 + 123658407 123658407 123658407 GCCCAGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTTATACTCTATTGGTTAGGCTGGTATC GCCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTTATACTCTATTGGTTAGGCTGGTATC A G GTF2H3 Ensembl:ENSG00000111358 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs954984315 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93528,RMVar_hsa_circ_161385,RMVar_hsa_circ_374063,RMVar_hsa_circ_161392 35537 RMVar_ID_35537 Human_SNP_ID_518989414 A-to-I Human chr12 + 123661520 123661520 123661520 AAAATTAGCCATGCGAAGTAGCAGGTGCCTGTAGTTCCAGCTACTCGGGAGGCTGAGGCAAGAGA AAAATTAGCCATGCGAAGTAGCAGGTGCCTGTGGTTCCAGCTACTCGGGAGGCTGAGGCAAGAGA A G GTF2H3 Ensembl:ENSG00000111358 Protein coding 3'UTR GSE38233;GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,32596459 RNA-Seq:(High) rs1198424684 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4209874 35538 RMVar_ID_35538 Human_SNP_ID_518989422 A-to-I Human chr12 + 123661547 123661547 123661547 CCTGTAGTTCCAGCTACTCGGGAGGCTGAGGCAAGAGAATTGCTTGAATCCAGGAGGCAGAGGTT CCTGTAGTTCCAGCTACTCGGGAGGCTGAGGCGAGAGAATTGCTTGAATCCAGGAGGCAGAGGTT A G GTF2H3 Ensembl:ENSG00000111358 Protein coding 3'UTR GSE38233;GSE99789;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29796672,32596459 RNA-Seq:(High) rs1332417783 Functional Loss SNV dbSNP153 33..33 33 - - - 35539 RMVar_ID_35539 Human_SNP_ID_518989489 A-to-I Human chr12 + 123661768 123661767 123661768 CTGGGTTTCTGTTTTGTTTTGTTTTGTGAGACAGAGTCTCGCTCTGTTGCCCAGGCTGGGGTGCA CTGGGTTTCTGTTTTGTTTTGTTTTGTGAGAC_GAGTCTCGCTCTGTTGCCCAGGCTGGGGTGCA CA C GTF2H3 Ensembl:ENSG00000111358 Protein coding 3'UTR GSE38233;GSE107867 cultured B-cells;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 24183664,30559470 RNA-Seq:(High) rs1209870243 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_22369862,Human_RBP_ID_23156697,Human_RBP_ID_26413468 35540 RMVar_ID_35540 Human_SNP_ID_518989490 A-to-I Human chr12 + 123661768 123661768 123661768 CTGGGTTTCTGTTTTGTTTTGTTTTGTGAGACAGAGTCTCGCTCTGTTGCCCAGGCTGGGGTGCA CTGGGTTTCTGTTTTGTTTTGTTTTGTGAGACGGAGTCTCGCTCTGTTGCCCAGGCTGGGGTGCA A G GTF2H3 Ensembl:ENSG00000111358 Protein coding 3'UTR GSE38233;GSE107867 cultured B-cells;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 24183664,30559470 RNA-Seq:(High) rs1048265855 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22369862,Human_RBP_ID_23156697,Human_RBP_ID_26413468 35541 RMVar_ID_35541 Human_SNP_ID_518989514 A-to-I Human chr12 + 123661849 123661849 123661849 TCTCTGCAAGCTCTGTCTCCTGGGTTCACGCCATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGA TCTCTGCAAGCTCTGTCTCCTGGGTTCACGCCGTTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGA A G GTF2H3 Ensembl:ENSG00000111358 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1002934832 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_115625,Human_RBP_ID_22369862,Human_RBP_ID_26421886,Human_RBP_ID_27419859 35542 RMVar_ID_35542 Human_SNP_ID_518999429 A-to-I Human chr12 + 123700211 123700211 123700211 TTTTTTTATTATTTGTAGAAATGGGTTTCGCCATGTTGCCCAGGCTGGTCATTAACTCCTGGGCT TTTTTTTATTATTTGTAGAAATGGGTTTCGCCGTGTTGCCCAGGCTGGTCATTAACTCCTGGGCT A G TCTN2 Ensembl:ENSG00000168778 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs565136857 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11024,RMVar_hsa_circ_161398,RMVar_hsa_circ_306013,RMVar_hsa_circ_48537,RMVar_hsa_circ_161406,RMVar_hsa_circ_161407,RMVar_hsa_circ_332666,RMVar_hsa_circ_316788,RMVar_hsa_circ_307635,RMVar_hsa_circ_161424,RMVar_hsa_circ_161425,RMVar_hsa_circ_363749,RMVar_hsa_circ_23061,RMVar_hsa_circ_329657,RMVar_hsa_circ_161428,RMVar_hsa_circ_375493 35543 RMVar_ID_35543 Human_SNP_ID_519222107 A-to-I Human chr12 - 124530802 124530802 124530802 GCCCCTGCTGTATGCTGGGGCCTGCAGCTGGTATGTTCACTTTGGTTCATTTTACTTGGCAGTTT GCCCCTGCTGTATGCTGGGGCCTGCAGCTGGTGTGTTCACTTTGGTTCATTTTACTTGGCAGTTT T C NCOR2 Ensembl:ENSG00000196498 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs528805395 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21997,RMVar_hsa_circ_62283,RMVar_hsa_circ_379002 35544 RMVar_ID_35544 Human_SNP_ID_519228497 A-to-I Human chr12 - 124552137 124552137 124552137 GTTTTGATTTTTAGTAGAGATGAGGTGTCATTATGTTGCCCGGGCTGGTCTTGAACTCCTGAGCT GTTTTGATTTTTAGTAGAGATGAGGTGTCATTGTGTTGCCCGGGCTGGTCTTGAACTCCTGAGCT T C NCOR2 Ensembl:ENSG00000196498 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs563379791 Functional Loss SNV dbSNP153 33..33 33 - - - 35545 RMVar_ID_35545 Human_SNP_ID_519249040 A-to-I Human chr12 - 124628494 124628494 124628494 GGGAGTGGTGGTACCCACTTGTAATCCCAGCTACTTGGAGGCTGAGGCAGGAAAATCGCTTGAAC GGGAGTGGTGGTACCCACTTGTAATCCCAGCTGCTTGGAGGCTGAGGCAGGAAAATCGCTTGAAC T C lnc-NCOR2-3,lnc-NCOR2-3:2,lnc-NCOR2-3:3,lnc-NCOR2-3:4,lnc-NCOR2-3:5 RNACentral:URS0000D589F7,RNACentral:URS0000D5D877,RNACentral:URS0000D5BFC2,RNACentral:URS0000D5BBD6,RNACentral:URS0000D56EC2 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1471499133 Functional Loss SNV dbSNP153 33..33 33 - - - 35546 RMVar_ID_35546 Human_SNP_ID_519288598 A-to-I Human chr12 - 124783734 124783734 124783734 GCTGTGTTGCCCAGGCTGGAGTGCAGTGGCACAATCTTGGCTCACTGCAACCTCCACCTCCCGGG GCTGTGTTGCCCAGGCTGGAGTGCAGTGGCACTATCTTGGCTCACTGCAACCTCCACCTCCCGGG T A SCARB1 Ensembl:ENSG00000073060 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1409960974 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11870661 RMVar_hsa_circ_10216,RMVar_hsa_circ_71896 35547 RMVar_ID_35547 Human_SNP_ID_519288603 A-to-I Human chr12 - 124783778 124783778 124783778 TTTTATTTTTATTTTTTTTGGTTTCTTTTTTGAGATGGAGTCTTGCTGTGTTGCCCAGGCTGGAG TTTTATTTTTATTTTTTTTGGTTTCTTTTTTGGGATGGAGTCTTGCTGTGTTGCCCAGGCTGGAG T C SCARB1 Ensembl:ENSG00000073060 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1486067575 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6150208 RMVar_hsa_circ_10216,RMVar_hsa_circ_71896 35548 RMVar_ID_35548 Human_SNP_ID_519301833 A-to-I Human chr12 - 124834821 124834821 124834821 TCACTGCAGCCTCGACCTTCTGGGCCCAAGCAATCCTCCTGCCTCAGCCTCCCAAGTAGCTGGGA TCACTGCAGCCTCGACCTTCTGGGCCCAAGCAGTCCTCCTGCCTCAGCCTCCCAAGTAGCTGGGA T C SCARB1 Ensembl:ENSG00000073060 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1343975304 Functional Loss SNV dbSNP153 33..33 33 - - - 35549 RMVar_ID_35549 Human_SNP_ID_519322720 A-to-I Human chr12 - 124912716 124912716 124912716 CCTGACCAGCAGAGGTTGATCTTTGCCGGAAAACAGCTGGAAGATGGTCGTACCCTGTCTGACTA CCTGACCAGCAGAGGTTGATCTTTGCCGGAAAGCAGCTGGAAGATGGTCGTACCCTGTCTGACTA T C UBC Ensembl:ENSG00000150991 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-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 35550 RMVar_ID_35550 Human_SNP_ID_519322919 A-to-I Human chr12 + 124913220 124913220 124913220 AACCTCTGCTGATCAGGAGGAATGCCTTCCTTATCTTGGATCTTTGCCTTGACATTCTCGATGGT AACCTCTGCTGATCAGGAGGAATGCCTTCCTTGTCTTGGATCTTTGCCTTGACATTCTCGATGGT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs370055957 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 35551 RMVar_ID_35551 Human_SNP_ID_519343568 A-to-I Human chr12 - 124979201 124979201 124979201 ACTACGCTTGGCTAACTTTGTATTTTTTTTGTAGAGACGGGGTTTTGCCATGTTGCCCAGGCTGG ACTACGCTTGGCTAACTTTGTATTTTTTTTGTGGAGACGGGGTTTTGCCATGTTGCCCAGGCTGG T C DHX37 Ensembl:ENSG00000150990 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs527811906 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73533,RMVar_hsa_circ_120739,RMVar_hsa_circ_161604,RMVar_hsa_circ_9280,RMVar_hsa_circ_313598 35552 RMVar_ID_35552 Human_SNP_ID_519345708 A-to-I Human chr12 - 124986635 124986635 124986635 AAGATCTCGGCTCACTGCAACCTCCACCTCCCAGTTTCAAGAGATTCTCCTGTCTCAGCCTCCCA AAGATCTCGGCTCACTGCAACCTCCACCTCCCGGTTTCAAGAGATTCTCCTGTCTCAGCCTCCCA T C DHX37 Ensembl:ENSG00000150990 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs747935710 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120739,RMVar_hsa_circ_161604 35553 RMVar_ID_35553 Human_SNP_ID_519348620 A-to-I Human chr12 + 124996876 124996876 124996876 TGCCGCCCAGGTTCAAACAATTCTCCTGCCTCAGCCCCCTGAGTAGCTGGGATTACAGGCGTGTG TGCCGCCCAGGTTCAAACAATTCTCCTGCCTCGGCCCCCTGAGTAGCTGGGATTACAGGCGTGTG A G BRI3BP Ensembl:ENSG00000184992 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs941884816 Functional Loss SNV dbSNP153 33..33 33 - - - 35554 RMVar_ID_35554 Human_SNP_ID_519349031 A-to-I Human chr12 + 124998206 124998205 124998206 CCCAGCTACTTGGGAGGCTGAGGCAGGAGAATAGATTGAGCCCGGGAGGCTGACGTTGCGGTGAG CCCAGCTACTTGGGAGGCTGAGGCAGGAGAAT_GATTGAGCCCGGGAGGCTGACGTTGCGGTGAG TA T BRI3BP Ensembl:ENSG00000184992 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs869146845 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_11871873,Human_RBP_ID_17561339 35555 RMVar_ID_35555 Human_SNP_ID_519349034 A-to-I Human chr12 + 124998206 124998206 124998206 CCCAGCTACTTGGGAGGCTGAGGCAGGAGAATAGATTGAGCCCGGGAGGCTGACGTTGCGGTGAG CCCAGCTACTTGGGAGGCTGAGGCAGGAGAATGGATTGAGCCCGGGAGGCTGACGTTGCGGTGAG A G BRI3BP Ensembl:ENSG00000184992 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1555216187 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11871873,Human_RBP_ID_17561339 35556 RMVar_ID_35556 Human_SNP_ID_519349197 A-to-I Human chr12 + 124998895 124998895 124998895 GCCCAGGAGTTTGAGACCAGCCTGGGCAACATAGTGAGACCCCATCTCTACGAAAAACCAAAACC GCCCAGGAGTTTGAGACCAGCCTGGGCAACATGGTGAGACCCCATCTCTACGAAAAACCAAAACC A G BRI3BP Ensembl:ENSG00000184992 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1373642042 Functional Loss SNV dbSNP153 33..33 33 - - - 35557 RMVar_ID_35557 Human_SNP_ID_519349341 A-to-I Human chr12 + 124999482 124999482 124999482 GTCTCCCTCTGTCGCCCAGGCTGGAGTGCAGTAGCTCAATCTTGGCTCACTGCAGTCTCTACCTC GTCTCCCTCTGTCGCCCAGGCTGGAGTGCAGTGGCTCAATCTTGGCTCACTGCAGTCTCTACCTC A G BRI3BP Ensembl:ENSG00000184992 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1476634337 Functional Loss SNV dbSNP153 33..33 33 - - - 35558 RMVar_ID_35558 Human_SNP_ID_519350046 A-to-I Human chr12 + 125001489 125001489 125001489 TCAAGCGATCCTCCCACCTTAACCTCCTGAGTAGCTGGGCTTACAAGCATGTGCCACCATGCCTA TCAAGCGATCCTCCCACCTTAACCTCCTGAGTGGCTGGGCTTACAAGCATGTGCCACCATGCCTA A G BRI3BP Ensembl:ENSG00000184992 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1468425719 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11871938 35559 RMVar_ID_35559 Human_SNP_ID_519350164 A-to-I Human chr12 + 125001919 125001919 125001919 TACTTTTTTCCTTTGCCCCAACTCCCAGCCTTAAGCAACTGCCAATCTGCTTTCTGTCTCTATTT TACTTTTTTCCTTTGCCCCAACTCCCAGCCTTGAGCAACTGCCAATCTGCTTTCTGTCTCTATTT A G BRI3BP Ensembl:ENSG00000184992 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs917739263 Functional Loss SNV dbSNP153 33..33 33 - - - 35560 RMVar_ID_35560 Human_SNP_ID_519350897 A-to-I Human chr12 + 125004212 125004211 125004212 AAAATTTTTTTGAGACAAGGTCTTGCTTTGTCACCCAGACTGGAGTGCAGTGGCACGAACACAGC AAAATTTTTTTGAGACAAGGTCTTGCTTTGTC_CCCAGACTGGAGTGCAGTGGCACGAACACAGC CA C BRI3BP Ensembl:ENSG00000184992 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1417854348 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_195886 35561 RMVar_ID_35561 Human_SNP_ID_519350907 A-to-I Human chr12 + 125004267 125004266 125004267 CGAACACAGCTCACTTGCAGCTTCAACCTCCCAGGTTCGATGATCCCCCAGCCTTCTCCCGAGTA CGAACACAGCTCACTTGCAGCTTCAACCTCCC_GGTTCGATGATCCCCCAGCCTTCTCCCGAGTA CA C BRI3BP Ensembl:ENSG00000184992 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1437090379 Functional Loss DEL dbSNP153 33..33 33 - - - 35562 RMVar_ID_35562 Human_SNP_ID_519350908 A-to-I Human chr12 + 125004267 125004267 125004267 CGAACACAGCTCACTTGCAGCTTCAACCTCCCAGGTTCGATGATCCCCCAGCCTTCTCCCGAGTA CGAACACAGCTCACTTGCAGCTTCAACCTCCCGGGTTCGATGATCCCCCAGCCTTCTCCCGAGTA A G BRI3BP Ensembl:ENSG00000184992 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1270643251 Functional Loss SNV dbSNP153 33..33 33 - - - 35563 RMVar_ID_35563 Human_SNP_ID_519350913 A-to-I Human chr12 + 125004284 125004284 125004284 CAGCTTCAACCTCCCAGGTTCGATGATCCCCCAGCCTTCTCCCGAGTAGCTGGAACCACAGGTAC CAGCTTCAACCTCCCAGGTTCGATGATCCCCCGGCCTTCTCCCGAGTAGCTGGAACCACAGGTAC A G BRI3BP Ensembl:ENSG00000184992 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1229341794 Functional Loss SNV dbSNP153 33..33 33 - - - 35564 RMVar_ID_35564 Human_SNP_ID_519351057 A-to-I Human chr12 + 125005026 125005026 125005026 TGCCATCACACCCGGCTAAGTTTTGTGTTTTTAGTAGAGTCAAGAGGTTTCACCATGTTGGCCAG TGCCATCACACCCGGCTAAGTTTTGTGTTTTTGGTAGAGTCAAGAGGTTTCACCATGTTGGCCAG A G BRI3BP Ensembl:ENSG00000184992 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1044046749 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11872020,Human_RBP_ID_24947216 35565 RMVar_ID_35565 Human_SNP_ID_519351058 A-to-I Human chr12 + 125005029 125005028 125005030 CATCACACCCGGCTAAGTTTTGTGTTTTTAGTAGAGTCAAGAGGTTTCACCATGTTGGCCAGGCT CATCACACCCGGCTAAGTTTTGTGTTTTTAGT__AGTCAAGAGGTTTCACCATGTTGGCCAGGCT TAG T BRI3BP Ensembl:ENSG00000184992 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1413806192 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_11872020 35566 RMVar_ID_35566 Human_SNP_ID_519351059 A-to-I Human chr12 + 125005029 125005029 125005029 CATCACACCCGGCTAAGTTTTGTGTTTTTAGTAGAGTCAAGAGGTTTCACCATGTTGGCCAGGCT CATCACACCCGGCTAAGTTTTGTGTTTTTAGTGGAGTCAAGAGGTTTCACCATGTTGGCCAGGCT A G BRI3BP Ensembl:ENSG00000184992 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1373304920 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11872020 35567 RMVar_ID_35567 Human_SNP_ID_519351653 A-to-I Human chr12 + 125007428 125007428 125007428 AAAACTAGCCAGGCTTGGTGGCATGTGTCTGTAATTCCAGTTACTCAGGAGGCTAAGGCAAGAGA AAAACTAGCCAGGCTTGGTGGCATGTGTCTGTGATTCCAGTTACTCAGGAGGCTAAGGCAAGAGA A G BRI3BP Ensembl:ENSG00000184992 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1278087962 Functional Loss SNV dbSNP153 33..33 33 - - - 35568 RMVar_ID_35568 Human_SNP_ID_519351657 A-to-I Human chr12 + 125007442 125007442 125007442 TTGGTGGCATGTGTCTGTAATTCCAGTTACTCAGGAGGCTAAGGCAAGAGAATTGCTTGGACCTG TTGGTGGCATGTGTCTGTAATTCCAGTTACTCGGGAGGCTAAGGCAAGAGAATTGCTTGGACCTG A G BRI3BP Ensembl:ENSG00000184992 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1199174825 Functional Loss SNV dbSNP153 33..33 33 - - - 35569 RMVar_ID_35569 Human_SNP_ID_519352395 A-to-I Human chr12 + 125009925 125009925 125009925 GCAGTTCGAGACCAGCCTGGCCAGCATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGC GCAGTTCGAGACCAGCCTGGCCAGCATGGTGACACCCCATCTCTACTAAAAATACAAAAATTAGC A C BRI3BP Ensembl:ENSG00000184992 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1036516550 Functional Loss SNV dbSNP153 33..33 33 - - - 35570 RMVar_ID_35570 Human_SNP_ID_519352896 A-to-I Human chr12 + 125012066 125012066 125012066 ATAATAAAGCCTGGTGTGGTGGCTGCACCTGTAGCCCTAGCTACTTGGGAAGCTAAGGCAGGATT ATAATAAAGCCTGGTGTGGTGGCTGCACCTGTTGCCCTAGCTACTTGGGAAGCTAAGGCAGGATT A T BRI3BP Ensembl:ENSG00000184992 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs533313218 Functional Loss SNV dbSNP153 33..33 33 - - - 35571 RMVar_ID_35571 Human_SNP_ID_519353612 A-to-I Human chr12 + 125014896 125014896 125014896 GCTCGTGATCCTCCCACCTCAGCCTCCCGAGTAGCTGGGACCACAGGCCCATGCCACCACACCTG GCTCGTGATCCTCCCACCTCAGCCTCCCGAGTGGCTGGGACCACAGGCCCATGCCACCACACCTG A G BRI3BP Ensembl:ENSG00000184992 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1163790348 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_161606 35572 RMVar_ID_35572 Human_SNP_ID_519354067 A-to-I Human chr12 + 125016655 125016655 125016655 TCAAGTGATTCTCCTGCCCCAGCCTGCCAAGTAGCTGGGATTACAGGCATGCACCACCACACCCG TCAAGTGATTCTCCTGCCCCAGCCTGCCAAGTGGCTGGGATTACAGGCATGCACCACCACACCCG A G BRI3BP Ensembl:ENSG00000184992 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1378857739 Functional Loss SNV dbSNP153 33..33 33 - - - 35573 RMVar_ID_35573 Human_SNP_ID_519354068 A-to-I Human chr12 + 125016655 125016655 125016655 TCAAGTGATTCTCCTGCCCCAGCCTGCCAAGTAGCTGGGATTACAGGCATGCACCACCACACCCG TCAAGTGATTCTCCTGCCCCAGCCTGCCAAGTTGCTGGGATTACAGGCATGCACCACCACACCCG A T BRI3BP Ensembl:ENSG00000184992 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1378857739 Functional Loss SNV dbSNP153 33..33 33 - - - 35574 RMVar_ID_35574 Human_SNP_ID_519356871 A-to-I Human chr12 + 125026680 125026680 125026680 TTTTTTAAAAAAGAAAGCCCTAGGCCAGGCGCAGTGGCTGATGCCTGTAATCCCAGCGCTTTGGG TTTTTTAAAAAAGAAAGCCCTAGGCCAGGCGCCGTGGCTGATGCCTGTAATCCCAGCGCTTTGGG A C BRI3BP Ensembl:ENSG00000184992 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1387788858 Functional Loss SNV dbSNP153 33..33 33 - - - 35575 RMVar_ID_35575 Human_SNP_ID_519357056 A-to-I Human chr12 + 125027396 125027396 125027396 GGATATTTAAGATTTGCTGGAGCAGGCTGGGCAGGGTGGCTCACCCCTATAATCCCAACACTTTG GGATATTTAAGATTTGCTGGAGCAGGCTGGGCCGGGTGGCTCACCCCTATAATCCCAACACTTTG A C BRI3BP Ensembl:ENSG00000184992 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs111457986 Functional Loss SNV dbSNP153 33..33 33 - - - 35576 RMVar_ID_35576 Human_SNP_ID_519357062 A-to-I Human chr12 + 125027412 125027412 125027412 CTGGAGCAGGCTGGGCAGGGTGGCTCACCCCTATAATCCCAACACTTTGGGAGGCCAAGGCAGGT CTGGAGCAGGCTGGGCAGGGTGGCTCACCCCTGTAATCCCAACACTTTGGGAGGCCAAGGCAGGT A G BRI3BP Ensembl:ENSG00000184992 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1421209837 Functional Loss SNV dbSNP153 33..33 33 - - - 35577 RMVar_ID_35577 Human_SNP_ID_519357070 A-to-I Human chr12 + 125027441 125027441 125027441 CCTATAATCCCAACACTTTGGGAGGCCAAGGCAGGTGGATCACCTGAGGTCAGGAGTTTGAGACC CCTATAATCCCAACACTTTGGGAGGCCAAGGCGGGTGGATCACCTGAGGTCAGGAGTTTGAGACC A G BRI3BP Ensembl:ENSG00000184992 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1351230401 Functional Loss SNV dbSNP153 33..33 33 - - - 35578 RMVar_ID_35578 Human_SNP_ID_519357076 A-to-I Human chr12 + 125027460 125027460 125027460 GGGAGGCCAAGGCAGGTGGATCACCTGAGGTCAGGAGTTTGAGACCAGCCCGGCCAACAGAGTGA GGGAGGCCAAGGCAGGTGGATCACCTGAGGTCGGGAGTTTGAGACCAGCCCGGCCAACAGAGTGA A G BRI3BP Ensembl:ENSG00000184992 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs927489042 Functional Loss SNV dbSNP153 33..33 33 - - - 35579 RMVar_ID_35579 Human_SNP_ID_519357087 A-to-I Human chr12 + 125027483 125027483 125027483 CCTGAGGTCAGGAGTTTGAGACCAGCCCGGCCAACAGAGTGAAACCCCGTCTCTACTAAAAATAC CCTGAGGTCAGGAGTTTGAGACCAGCCCGGCCGACAGAGTGAAACCCCGTCTCTACTAAAAATAC A G BRI3BP Ensembl:ENSG00000184992 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,31158229,31158229,31158229,31158229,31158229,31158229 RNA-Seq:(High) rs957533600 Functional Loss SNV dbSNP153 33..33 33 - - - 35580 RMVar_ID_35580 Human_SNP_ID_519357089 A-to-I Human chr12 + 125027488 125027488 125027488 GGTCAGGAGTTTGAGACCAGCCCGGCCAACAGAGTGAAACCCCGTCTCTACTAAAAATACAAAAA GGTCAGGAGTTTGAGACCAGCCCGGCCAACAGGGTGAAACCCCGTCTCTACTAAAAATACAAAAA A G BRI3BP Ensembl:ENSG00000184992 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs990308871 Functional Loss SNV dbSNP153 33..33 33 - - - 35581 RMVar_ID_35581 Human_SNP_ID_519357101 A-to-I Human chr12 + 125027527 125027527 125027527 CCCCGTCTCTACTAAAAATACAAAAATTAGCCAGGCCTGGTGGTGGGCGCCTGTGATCCCAGCTA CCCCGTCTCTACTAAAAATACAAAAATTAGCCCGGCCTGGTGGTGGGCGCCTGTGATCCCAGCTA A C BRI3BP Ensembl:ENSG00000184992 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs866169505 Functional Loss SNV dbSNP153 33..33 33 - - - 35582 RMVar_ID_35582 Human_SNP_ID_519357167 A-to-I Human chr12 + 125027767 125027767 125027767 TGGAGTGCAGTGGCACCATCTCGGCTCACTGCAAGCTCCGCCTCCTGGGTTCACGCCATTCTCCT TGGAGTGCAGTGGCACCATCTCGGCTCACTGCGAGCTCCGCCTCCTGGGTTCACGCCATTCTCCT A G BRI3BP Ensembl:ENSG00000184992 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1421550792 Functional Loss SNV dbSNP153 33..33 33 - - - 35583 RMVar_ID_35583 Human_SNP_ID_519357176 A-to-I Human chr12 + 125027792 125027792 125027792 TCACTGCAAGCTCCGCCTCCTGGGTTCACGCCATTCTCCTACCTCAGCCTCCCAAGTAGCCGGGA TCACTGCAAGCTCCGCCTCCTGGGTTCACGCCGTTCTCCTACCTCAGCCTCCCAAGTAGCCGGGA A G BRI3BP Ensembl:ENSG00000184992 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs543656909 Functional Loss SNV dbSNP153 33..33 33 - - - 35584 RMVar_ID_35584 Human_SNP_ID_519357245 A-to-I Human chr12 + 125027988 125027988 125027988 GGATTACAGGCGTGAGCCACCGCGCTGGGCCTAGATCAAATCTTTATCCATGCACATTGGAACAC GGATTACAGGCGTGAGCCACCGCGCTGGGCCTGGATCAAATCTTTATCCATGCACATTGGAACAC A G BRI3BP Ensembl:ENSG00000184992 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1467384576 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6150512,Human_RBP_ID_27420068 Human_miRNA_ID_1751324 35585 RMVar_ID_35585 Human_SNP_ID_519357522 A-to-I Human chr12 + 125029242 125029242 125029242 CCTTTCATAAATATACTTTCCAGGCTGGGTGCAGTGGCTCAAGCTTGTAATCCCAGCACTTTGGG CCTTTCATAAATATACTTTCCAGGCTGGGTGCGGTGGCTCAAGCTTGTAATCCCAGCACTTTGGG A G BRI3BP Ensembl:ENSG00000184992 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs537230892 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6150534,Human_RBP_ID_8778311,Human_RBP_ID_17812602 Human_miRNA_ID_1472746 35586 RMVar_ID_35586 Human_SNP_ID_519357523 A-to-I Human chr12 + 125029242 125029242 125029242 CCTTTCATAAATATACTTTCCAGGCTGGGTGCAGTGGCTCAAGCTTGTAATCCCAGCACTTTGGG CCTTTCATAAATATACTTTCCAGGCTGGGTGCTGTGGCTCAAGCTTGTAATCCCAGCACTTTGGG A T BRI3BP Ensembl:ENSG00000184992 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs537230892 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6150534,Human_RBP_ID_8778311,Human_RBP_ID_17812602 Human_miRNA_ID_1472746 35587 RMVar_ID_35587 Human_SNP_ID_519357605 A-to-I Human chr12 + 125029389 125029389 125029389 ATACAAAAAAAAAAAAAAAAAAAAAAATAGCCAGGTGTGGTGGTGGGTTCCTGTAGTCCCAGCTA ATACAAAAAAAAAAAAAAAAAAAAAAATAGCCGGGTGTGGTGGTGGGTTCCTGTAGTCCCAGCTA A G BRI3BP Ensembl:ENSG00000184992 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1304930495 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_414592,Human_RBP_ID_4211048,Human_RBP_ID_6150535,Human_RBP_ID_26423317 35588 RMVar_ID_35588 Human_SNP_ID_519357612 A-to-I Human chr12 + 125029417 125029417 125029417 AGCCAGGTGTGGTGGTGGGTTCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGTGGGAGAATTGTA AGCCAGGTGTGGTGGTGGGTTCCTGTAGTCCCGGCTACTCAGGAGGCTGAGGTGGGAGAATTGTA A G BRI3BP Ensembl:ENSG00000184992 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs796213291 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6150535 35589 RMVar_ID_35589 Human_SNP_ID_519357614 A-to-I Human chr12 + 125029425 125029425 125029425 GTGGTGGTGGGTTCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGTGGGAGAATTGTATGAACCTG GTGGTGGTGGGTTCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGTGGGAGAATTGTATGAACCTG A G BRI3BP Ensembl:ENSG00000184992 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs974376501 Functional Loss SNV dbSNP153 33..33 33 - - - 35590 RMVar_ID_35590 Human_SNP_ID_519357701 A-to-I Human chr12 + 125029574 125029574 125029574 AAAAGTGTGTGTGTGTGTATATATATGTATATATATATACACACACACACACTTTCCAATACCAG AAAAGTGTGTGTGTGTGTATATATATGTATATGTATATACACACACACACACTTTCCAATACCAG A G BRI3BP Ensembl:ENSG00000184992 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1437186292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1235732,Human_RBP_ID_8066352,Human_RBP_ID_8778319,Human_RBP_ID_17469131 Human_miRNA_ID_62286,Human_miRNA_ID_561552 35591 RMVar_ID_35591 Human_SNP_ID_519371401 A-to-I Human chr12 + 125083685 125083681 125083685 TTTGTTTGTTTGTTTGTTTGAGACAGAGTCTCACTCGGTCGCCGAGGCTGGAGTGCAGTAGCACC TTTGTTTGTTTGTTTGTTTGAGACAGAGT____CTCGGTCGCCGAGGCTGGAGTGCAGTAGCACC TCTCA T AACS Ensembl:ENSG00000081760 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs778935515 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_92427,RMVar_hsa_circ_312386,RMVar_hsa_circ_334527,RMVar_hsa_circ_378230,RMVar_hsa_circ_332993,RMVar_hsa_circ_161612,RMVar_hsa_circ_161609,RMVar_hsa_circ_161610,RMVar_hsa_circ_161608,RMVar_hsa_circ_117511 35592 RMVar_ID_35592 Human_SNP_ID_519375387 A-to-I Human chr12 + 125098251 125098251 125098251 CCGGAGTTTGAGAGCAGCCTGGGCAACATGGCAAAACTCCATCTCTACAAAAAAGAAATAACTTA CCGGAGTTTGAGAGCAGCCTGGGCAACATGGCCAAACTCCATCTCTACAAAAAAGAAATAACTTA A C AACS Ensembl:ENSG00000081760 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs939826531 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92427,RMVar_hsa_circ_378230,RMVar_hsa_circ_332993,RMVar_hsa_circ_161612,RMVar_hsa_circ_161609,RMVar_hsa_circ_161610,RMVar_hsa_circ_117511,RMVar_hsa_circ_376522 35593 RMVar_ID_35593 Human_SNP_ID_519588119 A-to-I Human chr12 - 125962190 125962190 125962190 GACTGGGTAATTTATAAAGGAAAAGGAGGTTTAATGGACTCACAGTTCCACATGGCTAGGGAGGC GACTGGGTAATTTATAAAGGAAAAGGAGGTTTGATGGACTCACAGTTCCACATGGCTAGGGAGGC T C LINC00939 Ensembl:ENSG00000249267 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1188995426 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_351368 35594 RMVar_ID_35594 Human_SNP_ID_520324770 A-to-I Human chr12 - 128803443 128803442 128803443 TCTTCAAATGAGCTTGGGTTATTTCTCCCCCCAGCTTACTGTGAATAATAAATGAGGTGCTGTCT TCTTCAAATGAGCTTGGGTTATTTCTCCCCCC_GCTTACTGTGAATAATAAATGAGGTGCTGTCT CT C SLC15A4 Ensembl:ENSG00000139370 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs113729829 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_48308,RMVar_hsa_circ_161642,RMVar_hsa_circ_120627,RMVar_hsa_circ_84074,RMVar_hsa_circ_337280,RMVar_hsa_circ_370553,RMVar_hsa_circ_161641,RMVar_hsa_circ_369969,RMVar_hsa_circ_161647,RMVar_hsa_circ_161643,RMVar_hsa_circ_161645,RMVar_hsa_circ_161644,RMVar_hsa_circ_284043,RMVar_hsa_circ_369708,RMVar_hsa_circ_161648 35595 RMVar_ID_35595 Human_SNP_ID_520324773 A-to-I Human chr12 - 128803443 128803443 128803443 TCTTCAAATGAGCTTGGGTTATTTCTCCCCCCAGCTTACTGTGAATAATAAATGAGGTGCTGTCT TCTTCAAATGAGCTTGGGTTATTTCTCCCCCCGGCTTACTGTGAATAATAAATGAGGTGCTGTCT T C SLC15A4 Ensembl:ENSG00000139370 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10773577 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48308,RMVar_hsa_circ_161642,RMVar_hsa_circ_120627,RMVar_hsa_circ_84074,RMVar_hsa_circ_337280,RMVar_hsa_circ_370553,RMVar_hsa_circ_161641,RMVar_hsa_circ_369969,RMVar_hsa_circ_161647,RMVar_hsa_circ_161643,RMVar_hsa_circ_161645,RMVar_hsa_circ_161644,RMVar_hsa_circ_284043,RMVar_hsa_circ_369708,RMVar_hsa_circ_161648 35596 RMVar_ID_35596 Human_SNP_ID_520324774 A-to-I Human chr12 - 128803443 128803443 128803443 TCTTCAAATGAGCTTGGGTTATTTCTCCCCCCAGCTTACTGTGAATAATAAATGAGGTGCTGTCT TCTTCAAATGAGCTTGGGTTATTTCTCCCCCCCGCTTACTGTGAATAATAAATGAGGTGCTGTCT T G SLC15A4 Ensembl:ENSG00000139370 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10773577 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48308,RMVar_hsa_circ_161642,RMVar_hsa_circ_120627,RMVar_hsa_circ_84074,RMVar_hsa_circ_337280,RMVar_hsa_circ_370553,RMVar_hsa_circ_161641,RMVar_hsa_circ_369969,RMVar_hsa_circ_161647,RMVar_hsa_circ_161643,RMVar_hsa_circ_161645,RMVar_hsa_circ_161644,RMVar_hsa_circ_284043,RMVar_hsa_circ_369708,RMVar_hsa_circ_161648 35597 RMVar_ID_35597 Human_SNP_ID_520328202 A-to-I Human chr12 - 128815468 128815468 128815468 TTGGCCAGGCTGGTCTCGAACTCCATACCTCAAGTGATCCACACGCCTCAGCCTCCCAAAGTGCT TTGGCCAGGCTGGTCTCGAACTCCATACCTCAGGTGATCCACACGCCTCAGCCTCCCAAAGTGCT T C SLC15A4 Ensembl:ENSG00000139370 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982585297 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_161642,RMVar_hsa_circ_84074 35598 RMVar_ID_35598 Human_SNP_ID_520522022 A-to-I Human chr12 - 129524819 129524819 129524819 GACGGAGTCTCACTCTGTCGCTAGGCTGGAGTACAGTGGCGCAGTCTCCGCTCACTGCAACCTCC GACGGAGTCTCACTCTGTCGCTAGGCTGGAGTTCAGTGGCGCAGTCTCCGCTCACTGCAACCTCC T A TMEM132D Ensembl:ENSG00000151952 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs931264232 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90099,RMVar_hsa_circ_109184,RMVar_hsa_circ_99580,RMVar_hsa_circ_161673,RMVar_hsa_circ_161674,RMVar_hsa_circ_94959,RMVar_hsa_circ_161675,RMVar_hsa_circ_127157,RMVar_hsa_circ_161676,RMVar_hsa_circ_84096,RMVar_hsa_circ_161677,RMVar_hsa_circ_161678 35599 RMVar_ID_35599 Human_SNP_ID_520522023 A-to-I Human chr12 - 129524819 129524819 129524819 GACGGAGTCTCACTCTGTCGCTAGGCTGGAGTACAGTGGCGCAGTCTCCGCTCACTGCAACCTCC GACGGAGTCTCACTCTGTCGCTAGGCTGGAGTGCAGTGGCGCAGTCTCCGCTCACTGCAACCTCC T C TMEM132D Ensembl:ENSG00000151952 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs931264232 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90099,RMVar_hsa_circ_109184,RMVar_hsa_circ_99580,RMVar_hsa_circ_161673,RMVar_hsa_circ_161674,RMVar_hsa_circ_94959,RMVar_hsa_circ_161675,RMVar_hsa_circ_127157,RMVar_hsa_circ_161676,RMVar_hsa_circ_84096,RMVar_hsa_circ_161677,RMVar_hsa_circ_161678 35600 RMVar_ID_35600 Human_SNP_ID_493049429 A-to-I Human chr12 + 20385131 20385131 20385131 ATCACCACACTGTCTTCCACAATGGTTGAGCCAATTTACATTCCCACCACCAGTGTAAACGCGTT ATCACCACACTGTCTTCCACAATGGTTGAGCCGATTTACATTCCCACCACCAGTGTAAACGCGTT A G PDE3A Ensembl:ENSG00000172572 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1186907701 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24465114 35601 RMVar_ID_35601 Human_SNP_ID_493049430 A-to-I Human chr12 + 20385131 20385131 20385131 ATCACCACACTGTCTTCCACAATGGTTGAGCCAATTTACATTCCCACCACCAGTGTAAACGCGTT ATCACCACACTGTCTTCCACAATGGTTGAGCCTATTTACATTCCCACCACCAGTGTAAACGCGTT A T PDE3A Ensembl:ENSG00000172572 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1186907701 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24465114 35602 RMVar_ID_35602 Human_SNP_ID_493068838 A-to-I Human chr12 + 20462902 20462902 20462902 GCCTTGACCTTCCAGGCTCAAGGGATCCTCCTACTTCGGCCTCCTGAGTATACCACCATGCCAGG GCCTTGACCTTCCAGGCTCAAGGGATCCTCCTGCTTCGGCCTCCTGAGTATACCACCATGCCAGG A G PDE3A Ensembl:ENSG00000172572 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251952449 Functional Loss SNV dbSNP153 33..33 33 - - - 35603 RMVar_ID_35603 Human_SNP_ID_493074447 A-to-I Human chr12 + 20486673 20486673 20486673 TTTGTTTTTTTGAGACAGAGTCTTGCTCTGTCACCTGTGCTGGAGTGCAGTGGTGCAATCTCAAT TTTGTTTTTTTGAGACAGAGTCTTGCTCTGTCTCCTGTGCTGGAGTGCAGTGGTGCAATCTCAAT A T PDE3A Ensembl:ENSG00000172572 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs529655037 Functional Loss SNV dbSNP153 33..33 33 - - - 35604 RMVar_ID_35604 Human_SNP_ID_493074469 A-to-I Human chr12 + 20486727 20486727 20486727 GCAATCTCAATCCACTGCAACCCCCGCCTTCCAGGTTCAAGCAATTCTCATGCGTCAGCCTCCCA GCAATCTCAATCCACTGCAACCCCCGCCTTCCGGGTTCAAGCAATTCTCATGCGTCAGCCTCCCA A G PDE3A Ensembl:ENSG00000172572 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs999760749 Functional Loss SNV dbSNP153 33..33 33 - - - 35605 RMVar_ID_35605 Human_SNP_ID_493074470 A-to-I Human chr12 + 20486737 20486737 20486737 TCCACTGCAACCCCCGCCTTCCAGGTTCAAGCAATTCTCATGCGTCAGCCTCCCAGGTAGCTGGG TCCACTGCAACCCCCGCCTTCCAGGTTCAAGCGATTCTCATGCGTCAGCCTCCCAGGTAGCTGGG A G PDE3A Ensembl:ENSG00000172572 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1312116115 Functional Loss SNV dbSNP153 33..33 33 - - - 35606 RMVar_ID_35606 Human_SNP_ID_493075573 A-to-I Human chr12 + 20490980 20490980 20490980 AAAATTAGCCAGATATGACGGTATGTGCCTGTAGTCCTAGCTACTCAGGAGGCTGAGGCAGGAGG AAAATTAGCCAGATATGACGGTATGTGCCTGTCGTCCTAGCTACTCAGGAGGCTGAGGCAGGAGG A C PDE3A Ensembl:ENSG00000172572 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs937723575 Functional Loss SNV dbSNP153 33..33 33 - - - 35607 RMVar_ID_35607 Human_SNP_ID_493075820 A-to-I Human chr12 + 20492000 20492000 20492000 GACGATAATTTAGTACAGAGAGTTTTTTTTTGAGGCAGAGTCTCGCCGTGTTGCCCAGGCTGGAG GACGATAATTTAGTACAGAGAGTTTTTTTTTGTGGCAGAGTCTCGCCGTGTTGCCCAGGCTGGAG A T PDE3A Ensembl:ENSG00000172572 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs929941289 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2323912,Human_RBP_ID_11904032 35608 RMVar_ID_35608 Human_SNP_ID_493329411 A-to-I Human chr12 + 21440984 21440984 21440984 TATCACATTTACCGATTTGCATATTTTAAGCCATCTTTGCATCCCTGAATAAATCCCACTTGATT TATCACATTTACCGATTTGCATATTTTAAGCCGTCTTTGCATCCCTGAATAAATCCCACTTGATT A G PYROXD1 Ensembl:ENSG00000121350 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs535061389 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27383,RMVar_hsa_circ_48181,RMVar_hsa_circ_332970 35609 RMVar_ID_35609 Human_SNP_ID_493380282 A-to-I Human chr12 - 21642094 21642094 21642094 GTGGACATTCTTACGTATGTTACCTGGAAACTAAGTGGATTACCCAAACACCGCGTGATTGGAAG GTGGACATTCTTACGTATGTTACCTGGAAACTGAGTGGATTACCCAAACACCGCGTGATTGGAAG T C LDHB,AC010197.2 Ensembl:ENSG00000111716,Ensembl:ENSG00000285854 Protein coding,Protein coding CDS,CDS GSE56152 embryonic stem cells,wild type - 25708366 RNA-Seq:(High) rs1197679109 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_34318,Human_RBP_ID_416415,Human_RBP_ID_991301,Human_RBP_ID_1469594,Human_RBP_ID_1792441,Human_RBP_ID_4216600,Human_RBP_ID_8247620,Human_RBP_ID_8372683,Human_RBP_ID_8779823,Human_RBP_ID_9014749,Human_RBP_ID_17353458,Human_RBP_ID_17470084,Human_RBP_ID_17815515,Human_RBP_ID_18623878,Human_RBP_ID_22435804,Human_RBP_ID_22492979,Human_RBP_ID_22755844,Human_RBP_ID_23207572,Human_RBP_ID_23552160,Human_RBP_ID_24957415,Human_RBP_ID_26905108 Human_Splice_Rec_1345814,Human_Splice_Rec_1345884,Human_Splice_Rec_1345898,Human_Splice_Rec_1345912,Human_Splice_Rec_1345926 RMVar_hsa_circ_110020,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_155228,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 35610 RMVar_ID_35610 Human_SNP_ID_493380285 A-to-I Human chr12 - 21642110 21642110 21642110 ATTTCCAAAATTTTTAGTGGACATTCTTACGTATGTTACCTGGAAACTAAGTGGATTACCCAAAC ATTTCCAAAATTTTTAGTGGACATTCTTACGTGTGTTACCTGGAAACTAAGTGGATTACCCAAAC T C LDHB,AC010197.2 Ensembl:ENSG00000111716,Ensembl:ENSG00000285854 Protein coding,Protein coding CDS,CDS GSE56152 embryonic stem cells,wild type - 25708366 RNA-Seq:(High) rs1446544363 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_34318,Human_RBP_ID_228811,Human_RBP_ID_416415,Human_RBP_ID_991301,Human_RBP_ID_1469595,Human_RBP_ID_1792441,Human_RBP_ID_5461691,Human_RBP_ID_8247620,Human_RBP_ID_9675912,Human_RBP_ID_17241454,Human_RBP_ID_17356927,Human_RBP_ID_18623878,Human_RBP_ID_22435804,Human_RBP_ID_22755844,Human_RBP_ID_23208008,Human_RBP_ID_23552160,Human_RBP_ID_26321260 Human_Splice_Rec_1345814,Human_Splice_Rec_1345884,Human_Splice_Rec_1345898,Human_Splice_Rec_1345912,Human_Splice_Rec_1345926 RMVar_hsa_circ_110020,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_155228,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 35611 RMVar_ID_35611 Human_SNP_ID_493380288 A-to-I Human chr12 + 21642115 21642115 21642115 GGTAATCCACTTAGTTTCCAGGTAACATACGTAAGAATGTCCACTAAAAATTTTGGAAATAATAT GGTAATCCACTTAGTTTCCAGGTAACATACGTGAGAATGTCCACTAAAAATTTTGGAAATAATAT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs200362342 Functional Loss SNV dbSNP153 33..33 33 - - - 35612 RMVar_ID_35612 Human_SNP_ID_493480272 A-to-I Human chr12 + 22053950 22053949 22053951 TTGTTGTTGTTTTTTGTCTTTTTTTTTGAGACAGGGTCTCGCTGTGTCTCTCAGGCTGGAGTGCA TTGTTGTTGTTTTTTGTCTTTTTTTTTGAGAC__GGTCTCGCTGTGTCTCTCAGGCTGGAGTGCA CAG C CMAS Ensembl:ENSG00000111726 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1365396239 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_124970,RMVar_hsa_circ_155243 35613 RMVar_ID_35613 Human_SNP_ID_493480273 A-to-I Human chr12 + 22053950 22053950 22053950 TTGTTGTTGTTTTTTGTCTTTTTTTTTGAGACAGGGTCTCGCTGTGTCTCTCAGGCTGGAGTGCA TTGTTGTTGTTTTTTGTCTTTTTTTTTGAGACGGGGTCTCGCTGTGTCTCTCAGGCTGGAGTGCA A G CMAS Ensembl:ENSG00000111726 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388503852 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124970,RMVar_hsa_circ_155243 35614 RMVar_ID_35614 Human_SNP_ID_493481272 A-to-I Human chr12 + 22058027 22058027 22058027 ATTTGTGTTTTTAGTGGAGATGGCGTTTCACTATGTTGGCTGGGCTGCTCTCGAACTCCTGACCT ATTTGTGTTTTTAGTGGAGATGGCGTTTCACTGTGTTGGCTGGGCTGCTCTCGAACTCCTGACCT A G CMAS Ensembl:ENSG00000111726 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs908356314 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_68254,RMVar_hsa_circ_124970,RMVar_hsa_circ_155243,RMVar_hsa_circ_332098,RMVar_hsa_circ_2952,RMVar_hsa_circ_40692 35615 RMVar_ID_35615 Human_SNP_ID_493576667 A-to-I Human chr12 - 22460851 22460851 22460851 CTGTGGGCCAGGTTTGGTGGCTCATACCTGCAATCCCACCACTTTGGGAGACCAAGGCAGGCGGA CTGTGGGCCAGGTTTGGTGGCTCATACCTGCAGTCCCACCACTTTGGGAGACCAAGGCAGGCGGA T C AC053513.2,C2CD5 Ensembl:ENSG00000256973,Ensembl:ENSG00000111731 lincRNA,Protein coding intron,intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs775810745 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28859,RMVar_hsa_circ_6786,RMVar_hsa_circ_155249,RMVar_hsa_circ_155250,RMVar_hsa_circ_281561,RMVar_hsa_circ_336506,RMVar_hsa_circ_334708,RMVar_hsa_circ_66939,RMVar_hsa_circ_40859,RMVar_hsa_circ_155252,RMVar_hsa_circ_155251,RMVar_hsa_circ_338201,RMVar_hsa_circ_11297,RMVar_hsa_circ_155254,RMVar_hsa_circ_26763 35616 RMVar_ID_35616 Human_SNP_ID_493586981 A-to-I Human chr12 - 22503553 22503553 22503553 TAAGCCGAGATCATGCCACTGCACTCCAGCCTAGGTGACAGAGGGAGACTCCATCTCAAAAAATA TAAGCCGAGATCATGCCACTGCACTCCAGCCTGGGTGACAGAGGGAGACTCCATCTCAAAAAATA T C C2CD5 Ensembl:ENSG00000111731 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1456457368 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28859,RMVar_hsa_circ_155250,RMVar_hsa_circ_281561,RMVar_hsa_circ_66939,RMVar_hsa_circ_40859,RMVar_hsa_circ_155251,RMVar_hsa_circ_338201,RMVar_hsa_circ_279230,RMVar_hsa_circ_340688,RMVar_hsa_circ_349291,RMVar_hsa_circ_279446,RMVar_hsa_circ_37686,RMVar_hsa_circ_155258,RMVar_hsa_circ_23841,RMVar_hsa_circ_9703,RMVar_hsa_circ_18553,RMVar_hsa_circ_81054,RMVar_hsa_circ_61739,RMVar_hsa_circ_155261,RMVar_hsa_circ_358413,RMVar_hsa_circ_64599,RMVar_hsa_circ_285502,RMVar_hsa_circ_352810,RMVar_hsa_circ_66293,RMVar_hsa_circ_293739,RMVar_hsa_circ_53042,RMVar_hsa_circ_298120,RMVar_hsa_circ_37492,RMVar_hsa_circ_281536,RMVar_hsa_circ_4104,RMVar_hsa_circ_3036,RMVar_hsa_circ_155266,RMVar_hsa_circ_155265,RMVar_hsa_circ_355845,RMVar_hsa_circ_282675,RMVar_hsa_circ_155271,RMVar_hsa_circ_270872,RMVar_hsa_circ_277451,RMVar_hsa_circ_155273,RMVar_hsa_circ_278361,RMVar_hsa_circ_155274 35617 RMVar_ID_35617 Human_SNP_ID_493619951 A-to-I Human chr12 + 22639493 22639493 22639493 GAGATCAGGAGCTCTAGACCAGCCTGGCCAACATGGCGAAACCCCATCTCTACTAAAAATACAAA GAGATCAGGAGCTCTAGACCAGCCTGGCCAACGTGGCGAAACCCCATCTCTACTAAAAATACAAA A G ETNK1 Ensembl:ENSG00000139163 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355456058 Functional Loss SNV dbSNP153 33..33 33 - - - 35618 RMVar_ID_35618 Human_SNP_ID_493961277 A-to-I Human chr12 - 23980010 23980010 23980010 GGCCAGGAGTCTGAGAACATCCTGGGCAATATAGCGAGATTCTGTCTCTACTATCTATCTATCTA GGCCAGGAGTCTGAGAACATCCTGGGCAATATGGCGAGATTCTGTCTCTACTATCTATCTATCTA T C SOX5 Ensembl:ENSG00000134532 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1188063536 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56469,RMVar_hsa_circ_60625,RMVar_hsa_circ_14868,RMVar_hsa_circ_318132,RMVar_hsa_circ_327748,RMVar_hsa_circ_367729,RMVar_hsa_circ_359270 35619 RMVar_ID_35619 Human_SNP_ID_494021526 A-to-I Human chr12 - 24213419 24213418 24213419 TTTTTCTTTTTCTTTTTTTTTTTTTTTTTTTTAGCATTTCAAGAAATAGATAATATCAAGGACAT TTTTTCTTTTTCTTTTTTTTTTTTTTTTTTTT_GCATTTCAAGAAATAGATAATATCAAGGACAT CT C SOX5 Ensembl:ENSG00000134532 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1162868042 Functional Loss DEL dbSNP153 33..33 33 - - - Human_Splice_Rec_1347137,Human_Splice_Rec_1347261,Human_Splice_Rec_1347295,Human_Splice_Rec_1347305 RMVar_hsa_circ_56469,RMVar_hsa_circ_14868,RMVar_hsa_circ_327748,RMVar_hsa_circ_155311,RMVar_hsa_circ_155313,RMVar_hsa_circ_274535,RMVar_hsa_circ_301541,RMVar_hsa_circ_293609,RMVar_hsa_circ_155314,RMVar_hsa_circ_155312 35620 RMVar_ID_35620 Human_SNP_ID_494021527 A-to-I Human chr12 - 24213419 24213418 24213420 TTTTTCTTTTTCTTTTTTTTTTTTTTTTTTTTAGCATTTCAAGAAATAGATAATATCAAGGACAT TTTTTCTTTTTCTTTTTTTTTTTTTTTTTTT__GCATTTCAAGAAATAGATAATATCAAGGACAT CTA C SOX5 Ensembl:ENSG00000134532 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1491464886 Functional Loss DEL dbSNP153 32..33 33 - - - Human_Splice_Rec_1347137,Human_Splice_Rec_1347261,Human_Splice_Rec_1347295,Human_Splice_Rec_1347305 RMVar_hsa_circ_56469,RMVar_hsa_circ_14868,RMVar_hsa_circ_327748,RMVar_hsa_circ_155311,RMVar_hsa_circ_155313,RMVar_hsa_circ_274535,RMVar_hsa_circ_301541,RMVar_hsa_circ_293609,RMVar_hsa_circ_155314,RMVar_hsa_circ_155312 35621 RMVar_ID_35621 Human_SNP_ID_494021528 A-to-I Human chr12 - 24213419 24213419 24213419 TTTTTCTTTTTCTTTTTTTTTTTTTTTTTTTTAGCATTTCAAGAAATAGATAATATCAAGGACAT TTTTTCTTTTTCTTTTTTTTTTTTTTTTTTTTTGCATTTCAAGAAATAGATAATATCAAGGACAT T A SOX5 Ensembl:ENSG00000134532 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1364613071 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1347137,Human_Splice_Rec_1347261,Human_Splice_Rec_1347295,Human_Splice_Rec_1347305 RMVar_hsa_circ_56469,RMVar_hsa_circ_14868,RMVar_hsa_circ_327748,RMVar_hsa_circ_155311,RMVar_hsa_circ_155313,RMVar_hsa_circ_274535,RMVar_hsa_circ_301541,RMVar_hsa_circ_293609,RMVar_hsa_circ_155314,RMVar_hsa_circ_155312 35622 RMVar_ID_35622 Human_SNP_ID_494098085 A-to-I Human chr12 - 24518171 24518171 24518171 CCAGCTACTCGGGAGGCTGAGGCATGAGAAACACTGGAAGCTGGGAGGTGGAGGTTGCAGTCAGT CCAGCTACTCGGGAGGCTGAGGCATGAGAAACGCTGGAAGCTGGGAGGTGGAGGTTGCAGTCAGT T C SOX5 Ensembl:ENSG00000134532 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs983195028 Functional Loss SNV dbSNP153 33..33 33 - - - 35623 RMVar_ID_35623 Human_SNP_ID_494172206 A-to-I Human chr12 - 24816887 24816887 24816887 ACTCCACCTCTTGTCAGCTCAGTGGCAGCATTAGATTCTCATAGGAGCACAAATCCTATTGTGAA ACTCCACCTCTTGTCAGCTCAGTGGCAGCATTTGATTCTCATAGGAGCACAAATCCTATTGTGAA T A BCAT1 Ensembl:ENSG00000060982 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1196352712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_359043 35624 RMVar_ID_35624 Human_SNP_ID_494174456 A-to-I Human chr12 - 24826096 24826096 24826096 GCAATTCTCCCACCTTGGCTTTCCATGTAGCTAGAACCACAGGTGCATGCCACCACATTCCACTA GCAATTCTCCCACCTTGGCTTTCCATGTAGCTGGAACCACAGGTGCATGCCACCACATTCCACTA T C BCAT1 Ensembl:ENSG00000060982 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1346765366 Functional Loss SNV dbSNP153 33..33 33 - - - 35625 RMVar_ID_35625 Human_SNP_ID_494190834 A-to-I Human chr12 - 24891887 24891887 24891887 AAAATTAGCCGGGCGTGGTGGCAGGCGCCTGTAGTCCAAGCTACTTAGGAGGCTGAGGCAGGAAA AAAATTAGCCGGGCGTGGTGGCAGGCGCCTGTGGTCCAAGCTACTTAGGAGGCTGAGGCAGGAAA T C BCAT1 Ensembl:ENSG00000060982 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1254948062 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_115247 RMVar_hsa_circ_23695,RMVar_hsa_circ_349071,RMVar_hsa_circ_347758,RMVar_hsa_circ_306384,RMVar_hsa_circ_155328,RMVar_hsa_circ_332966 35626 RMVar_ID_35626 Human_SNP_ID_494198313 A-to-I Human chr12 - 24922303 24922303 24922303 TCTTGTAGCTGGGCAAGGTGGCACATGCCTGTAGTCCCAGCTACTTGGGGGACTGAGGCAGGTGG TCTTGTAGCTGGGCAAGGTGGCACATGCCTGTGGTCCCAGCTACTTGGGGGACTGAGGCAGGTGG T C BCAT1 Ensembl:ENSG00000060982 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs563148582 Functional Loss SNV dbSNP153 33..33 33 - - - 35627 RMVar_ID_35627 Human_SNP_ID_494202528 A-to-I Human chr12 - 24939674 24939674 24939674 TGCCACCATGCTTGGCTAGTTTTTGTATTTTTAGTAGTGACGGAGTTTTGCCATGCTGGCCAGGC TGCCACCATGCTTGGCTAGTTTTTGTATTTTTGGTAGTGACGGAGTTTTGCCATGCTGGCCAGGC T C BCAT1 Ensembl:ENSG00000060982 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1191451391 Functional Loss SNV dbSNP153 33..33 33 - - - 35628 RMVar_ID_35628 Human_SNP_ID_494216137 A-to-I Human chr12 - 24995365 24995365 24995365 TGAGACCAACCTGGGCAACATAGAGAAACCCTATCTCTACCAAAAATACAAAATTAGCCAGGCAG TGAGACCAACCTGGGCAACATAGAGAAACCCTGTCTCTACCAAAAATACAAAATTAGCCAGGCAG T C C12orf77 Ensembl:ENSG00000226397 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs937929442 Functional Loss SNV dbSNP153 33..33 33 - - - 35629 RMVar_ID_35629 Human_SNP_ID_494216139 A-to-I Human chr12 - 24995371 24995371 24995371 TGAGTTTGAGACCAACCTGGGCAACATAGAGAAACCCTATCTCTACCAAAAATACAAAATTAGCC TGAGTTTGAGACCAACCTGGGCAACATAGAGACACCCTATCTCTACCAAAAATACAAAATTAGCC T G C12orf77 Ensembl:ENSG00000226397 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1231245980 Functional Loss SNV dbSNP153 33..33 33 - - - 35630 RMVar_ID_35630 Human_SNP_ID_494237493 A-to-I Human chr12 + 25080626 25080626 25080626 CACCCTCCTTGGCCTCCCAAAATGTTGGGATTACAGGTGTGAGCCACCGCGCCTGGCCAAGGAAA CACCCTCCTTGGCCTCCCAAAATGTTGGGATTTCAGGTGTGAGCCACCGCGCCTGGCCAAGGAAA A T LRMP Ensembl:ENSG00000118308 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1030719640 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1294,RMVar_hsa_circ_2553,RMVar_hsa_circ_358584,RMVar_hsa_circ_349896,RMVar_hsa_circ_155335,RMVar_hsa_circ_298774 35631 RMVar_ID_35631 Human_SNP_ID_494237854 A-to-I Human chr12 + 25082034 25082034 25082034 CTCCTGTCCCAGGTTCCTCAGTAGTTGGGACTACGGGTGCAAGCCACCACATTTGACTAATTAAA CTCCTGTCCCAGGTTCCTCAGTAGTTGGGACTTCGGGTGCAAGCCACCACATTTGACTAATTAAA A T LRMP Ensembl:ENSG00000118308 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs758963948 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1294,RMVar_hsa_circ_2553,RMVar_hsa_circ_358584,RMVar_hsa_circ_349896,RMVar_hsa_circ_155335,RMVar_hsa_circ_298774 35632 RMVar_ID_35632 Human_SNP_ID_494266991 A-to-I Human chr12 + 25196991 25196991 25196991 CCTGGATAACACAGTGAAACCCCGTCTCTACTAAAATAATACAAAAAATTAGCCGGGCGTGGTGA CCTGGATAACACAGTGAAACCCCGTCTCTACTGAAATAATACAAAAAATTAGCCGGGCGTGGTGA A G ETFRF1 Ensembl:ENSG00000205707 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1448139228 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113743,RMVar_hsa_circ_155340 35633 RMVar_ID_35633 Human_SNP_ID_494267181 A-to-I Human chr12 + 25197745 25197745 25197745 CTCCAGCCCTGGCCTCCCAAAGTGCTGAGATTACAGGTACAAGCCACCATGCCCAGCCTAAGAAT CTCCAGCCCTGGCCTCCCAAAGTGCTGAGATTGCAGGTACAAGCCACCATGCCCAGCCTAAGAAT A G ETFRF1 Ensembl:ENSG00000205707 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1014500519 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113743,RMVar_hsa_circ_155340 35634 RMVar_ID_35634 Human_SNP_ID_494546726 A-to-I Human chr12 - 26354955 26354955 26354955 GACAGACTTTGAGAACCACCAACTTGCCAGGTACGGTGGCTCACACCTGTAATCCCAGCACTTTG GACAGACTTTGAGAACCACCAACTTGCCAGGTGCGGTGGCTCACACCTGTAATCCCAGCACTTTG T C ITPR2 Ensembl:ENSG00000123104 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1396654109 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121970,RMVar_hsa_circ_264833,RMVar_hsa_circ_155351 35635 RMVar_ID_35635 Human_SNP_ID_494564036 A-to-I Human chr12 - 26430986 26430986 26430986 GTTAAGGGACCAAGAAATGAATAAGGCACAATAGTAAAGACCACCCAGGGATTTCTGAGTGGATG GTTAAGGGACCAAGAAATGAATAAGGCACAATGGTAAAGACCACCCAGGGATTTCTGAGTGGATG T C ITPR2 Ensembl:ENSG00000123104 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1201762678 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3806,RMVar_hsa_circ_70997,RMVar_hsa_circ_21493,RMVar_hsa_circ_73712,RMVar_hsa_circ_350617,RMVar_hsa_circ_361249,RMVar_hsa_circ_375791,RMVar_hsa_circ_367183,RMVar_hsa_circ_347557,RMVar_hsa_circ_312454,RMVar_hsa_circ_65942,RMVar_hsa_circ_67873,RMVar_hsa_circ_53795,RMVar_hsa_circ_65549,RMVar_hsa_circ_101286,RMVar_hsa_circ_155353,RMVar_hsa_circ_155354,RMVar_hsa_circ_344221,RMVar_hsa_circ_30679,RMVar_hsa_circ_58328,RMVar_hsa_circ_155355,RMVar_hsa_circ_359467,RMVar_hsa_circ_374652,RMVar_hsa_circ_378805,RMVar_hsa_circ_368488,RMVar_hsa_circ_358361,RMVar_hsa_circ_338001,RMVar_hsa_circ_57573,RMVar_hsa_circ_47625,RMVar_hsa_circ_63728,RMVar_hsa_circ_64939,RMVar_hsa_circ_54224,RMVar_hsa_circ_155357,RMVar_hsa_circ_22894,RMVar_hsa_circ_25918,RMVar_hsa_circ_155358,RMVar_hsa_circ_73744,RMVar_hsa_circ_362874,RMVar_hsa_circ_155356,RMVar_hsa_circ_302294,RMVar_hsa_circ_65627,RMVar_hsa_circ_78109,RMVar_hsa_circ_120526,RMVar_hsa_circ_56543,RMVar_hsa_circ_155360,RMVar_hsa_circ_363521,RMVar_hsa_circ_356299,RMVar_hsa_circ_364684,RMVar_hsa_circ_356218,RMVar_hsa_circ_111397,RMVar_hsa_circ_55909,RMVar_hsa_circ_72069,RMVar_hsa_circ_17573,RMVar_hsa_circ_155362,RMVar_hsa_circ_155363,RMVar_hsa_circ_155361 35636 RMVar_ID_35636 Human_SNP_ID_494593151 A-to-I Human chr12 - 26553747 26553747 26553747 GGAGTCTTGCTCTGTCACCCAGGCTGGAGTGCAGTGGCGCAATCTTGGCTCACTGCAAGCTCTGC GGAGTCTTGCTCTGTCACCCAGGCTGGAGTGCTGTGGCGCAATCTTGGCTCACTGCAAGCTCTGC T A ITPR2 Ensembl:ENSG00000123104 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1269027112 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3806,RMVar_hsa_circ_70997,RMVar_hsa_circ_21493,RMVar_hsa_circ_350617,RMVar_hsa_circ_361249,RMVar_hsa_circ_67873,RMVar_hsa_circ_53795,RMVar_hsa_circ_65549,RMVar_hsa_circ_101286,RMVar_hsa_circ_58328,RMVar_hsa_circ_155355,RMVar_hsa_circ_359467,RMVar_hsa_circ_368488,RMVar_hsa_circ_358361,RMVar_hsa_circ_57573,RMVar_hsa_circ_63728,RMVar_hsa_circ_54224,RMVar_hsa_circ_22894,RMVar_hsa_circ_73744,RMVar_hsa_circ_362874,RMVar_hsa_circ_363521,RMVar_hsa_circ_356299,RMVar_hsa_circ_111397,RMVar_hsa_circ_55909,RMVar_hsa_circ_72069,RMVar_hsa_circ_53517,RMVar_hsa_circ_94304,RMVar_hsa_circ_92486,RMVar_hsa_circ_364745,RMVar_hsa_circ_155363,RMVar_hsa_circ_96274,RMVar_hsa_circ_155365,RMVar_hsa_circ_56199,RMVar_hsa_circ_112326,RMVar_hsa_circ_155364,RMVar_hsa_circ_155370,RMVar_hsa_circ_76317,RMVar_hsa_circ_155369,RMVar_hsa_circ_317047,RMVar_hsa_circ_62072,RMVar_hsa_circ_155371,RMVar_hsa_circ_368690,RMVar_hsa_circ_331828,RMVar_hsa_circ_344489,RMVar_hsa_circ_327688,RMVar_hsa_circ_99699,RMVar_hsa_circ_63068,RMVar_hsa_circ_18017,RMVar_hsa_circ_69218,RMVar_hsa_circ_155372,RMVar_hsa_circ_301791,RMVar_hsa_circ_371332,RMVar_hsa_circ_107214,RMVar_hsa_circ_83121,RMVar_hsa_circ_81439,RMVar_hsa_circ_155374,RMVar_hsa_circ_155375,RMVar_hsa_circ_155373,RMVar_hsa_circ_361476,RMVar_hsa_circ_57451,RMVar_hsa_circ_155378,RMVar_hsa_circ_124380,RMVar_hsa_circ_155377,RMVar_hsa_circ_98876,RMVar_hsa_circ_356621,RMVar_hsa_circ_352142,RMVar_hsa_circ_155381,RMVar_hsa_circ_127093,RMVar_hsa_circ_312094,RMVar_hsa_circ_359510,RMVar_hsa_circ_269530,RMVar_hsa_circ_155379,RMVar_hsa_circ_265223,RMVar_hsa_circ_360892,RMVar_hsa_circ_339091,RMVar_hsa_circ_340058,RMVar_hsa_circ_326543,RMVar_hsa_circ_275155,RMVar_hsa_circ_290365,RMVar_hsa_circ_271613,RMVar_hsa_circ_57331,RMVar_hsa_circ_72770,RMVar_hsa_circ_103419,RMVar_hsa_circ_65349,RMVar_hsa_circ_54112,RMVar_hsa_circ_57024,RMVar_hsa_circ_155383,RMVar_hsa_circ_155385,RMVar_hsa_circ_53987,RMVar_hsa_circ_155384,RMVar_hsa_circ_155382,RMVar_hsa_circ_155380 35637 RMVar_ID_35637 Human_SNP_ID_494603854 A-to-I Human chr12 - 26596525 26596525 26596525 CTCCTGCCTCAGCCTCCCGAGTGGCTGGGATTACAGGCATGTGCCACCATGCTCAGCTAATTTTT CTCCTGCCTCAGCCTCCCGAGTGGCTGGGATTGCAGGCATGTGCCACCATGCTCAGCTAATTTTT T C ITPR2 Ensembl:ENSG00000123104 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1451103342 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3806,RMVar_hsa_circ_350617,RMVar_hsa_circ_361249,RMVar_hsa_circ_67873,RMVar_hsa_circ_65549,RMVar_hsa_circ_101286,RMVar_hsa_circ_58328,RMVar_hsa_circ_155355,RMVar_hsa_circ_359467,RMVar_hsa_circ_368488,RMVar_hsa_circ_358361,RMVar_hsa_circ_57573,RMVar_hsa_circ_22894,RMVar_hsa_circ_73744,RMVar_hsa_circ_362874,RMVar_hsa_circ_363521,RMVar_hsa_circ_356299,RMVar_hsa_circ_111397,RMVar_hsa_circ_72069,RMVar_hsa_circ_53517,RMVar_hsa_circ_94304,RMVar_hsa_circ_92486,RMVar_hsa_circ_364745,RMVar_hsa_circ_155363,RMVar_hsa_circ_96274,RMVar_hsa_circ_155365,RMVar_hsa_circ_56199,RMVar_hsa_circ_112326,RMVar_hsa_circ_155364,RMVar_hsa_circ_155370,RMVar_hsa_circ_76317,RMVar_hsa_circ_155369,RMVar_hsa_circ_317047,RMVar_hsa_circ_62072,RMVar_hsa_circ_155371,RMVar_hsa_circ_331828,RMVar_hsa_circ_344489,RMVar_hsa_circ_327688,RMVar_hsa_circ_99699,RMVar_hsa_circ_63068,RMVar_hsa_circ_18017,RMVar_hsa_circ_69218,RMVar_hsa_circ_155372,RMVar_hsa_circ_301791,RMVar_hsa_circ_371332,RMVar_hsa_circ_107214,RMVar_hsa_circ_83121,RMVar_hsa_circ_81439,RMVar_hsa_circ_155374,RMVar_hsa_circ_155375,RMVar_hsa_circ_155373,RMVar_hsa_circ_361476,RMVar_hsa_circ_57451,RMVar_hsa_circ_155378,RMVar_hsa_circ_124380,RMVar_hsa_circ_155377,RMVar_hsa_circ_98876,RMVar_hsa_circ_356621,RMVar_hsa_circ_352142,RMVar_hsa_circ_127093,RMVar_hsa_circ_312094,RMVar_hsa_circ_359510,RMVar_hsa_circ_155379,RMVar_hsa_circ_265223,RMVar_hsa_circ_360892,RMVar_hsa_circ_339091,RMVar_hsa_circ_275155,RMVar_hsa_circ_290365,RMVar_hsa_circ_271613,RMVar_hsa_circ_57331,RMVar_hsa_circ_72770,RMVar_hsa_circ_103419,RMVar_hsa_circ_65349,RMVar_hsa_circ_54112,RMVar_hsa_circ_57024,RMVar_hsa_circ_155383,RMVar_hsa_circ_155385,RMVar_hsa_circ_53987,RMVar_hsa_circ_155384,RMVar_hsa_circ_155382,RMVar_hsa_circ_25452,RMVar_hsa_circ_122448,RMVar_hsa_circ_355339,RMVar_hsa_circ_359859,RMVar_hsa_circ_355734,RMVar_hsa_circ_313614,RMVar_hsa_circ_267613,RMVar_hsa_circ_155387,RMVar_hsa_circ_77575,RMVar_hsa_circ_366712,RMVar_hsa_circ_155386,RMVar_hsa_circ_354261,RMVar_hsa_circ_320133,RMVar_hsa_circ_327296,RMVar_hsa_circ_306416,RMVar_hsa_circ_155389,RMVar_hsa_circ_282529,RMVar_hsa_circ_72564,RMVar_hsa_circ_155388,RMVar_hsa_circ_348007,RMVar_hsa_circ_361008,RMVar_hsa_circ_365628,RMVar_hsa_circ_289970,RMVar_hsa_circ_69244,RMVar_hsa_circ_72124,RMVar_hsa_circ_155390 35638 RMVar_ID_35638 Human_SNP_ID_494676646 A-to-I Human chr12 - 26909278 26909278 26909278 CAGCCCAGTGCAGCCTCTGCCTCTTGGGTTCAAGTGATTCTCCTGCCTCAGCATCCCGAGTAGCT CAGCCCAGTGCAGCCTCTGCCTCTTGGGTTCAGGTGATTCTCCTGCCTCAGCATCCCGAGTAGCT T C INTS13 Ensembl:ENSG00000064102 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1438027928 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_155419,RMVar_hsa_circ_112157 35639 RMVar_ID_35639 Human_SNP_ID_494677701 A-to-I Human chr12 - 26913639 26913639 26913639 ATCATGTGGAATGAATTAGAAACCCTTGTCAGAGCCCATATCAACAACTCAGAGAAACATCAAAG ATCATGTGGAATGAATTAGAAACCCTTGTCAGCGCCCATATCAACAACTCAGAGAAACATCAAAG T G INTS13 Ensembl:ENSG00000064102 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1565820199 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_33263,Human_RBP_ID_2329621,Human_RBP_ID_22572285 Human_Splice_Rec_1349120,Human_Splice_Rec_1349152 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 35640 RMVar_ID_35640 Human_SNP_ID_494677800 A-to-I Human chr12 - 26914081 26914078 26914081 AGTGTTATTGTGAAAGAATCTCTGACAGAAGAAGATGTGTTAAACTGTCAAAAAACAATATACAA AGTGTTATTGTGAAAGAATCTCTGACAGAAGA___TGTGTTAAACTGTCAAAAAACAATATACAA ATCT A INTS13 Ensembl:ENSG00000064102 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334876338 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_1469991,Human_RBP_ID_1793044 Human_Splice_Rec_1349118,Human_Splice_Rec_1349150,Human_Splice_Rec_1349170,Human_Splice_Rec_1349178 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 35641 RMVar_ID_35641 Human_SNP_ID_494679656 A-to-I Human chr12 - 26921898 26921898 26921898 TAATCCTAGCACTTTGGGAGGCCAAGGTGGGCAGATCACTTGAGGTCAGGAGTTCGAGACAAGCG TAATCCTAGCACTTTGGGAGGCCAAGGTGGGCGGATCACTTGAGGTCAGGAGTTCGAGACAAGCG T C INTS13 Ensembl:ENSG00000064102 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1432157603 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72430,RMVar_hsa_circ_360008,RMVar_hsa_circ_363111,RMVar_hsa_circ_99523,RMVar_hsa_circ_155424 35642 RMVar_ID_35642 Human_SNP_ID_494683153 A-to-I Human chr12 - 26936718 26936718 26936718 TTATATGGCAGAATCTTGCAGGCAGCATGTCGAGTTTGATATGCTGGTGAAGAATAGAACCCAAG TTATATGGCAGAATCTTGCAGGCAGCATGTCGTGTTTGATATGCTGGTGAAGAATAGAACCCAAG T A INTS13 Ensembl:ENSG00000064102 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1022170371 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9015469,Human_RBP_ID_9322457 Human_Splice_Rec_1349128,Human_Splice_Rec_1349188,Human_Splice_Rec_1349200 RMVar_hsa_circ_72430,RMVar_hsa_circ_19224,RMVar_hsa_circ_61728 35643 RMVar_ID_35643 Human_SNP_ID_494684748 A-to-I Human chr12 + 26942132 26942132 26942132 TCGGCTCACTGCATCCTCCACCTTCCGGGCTCAAGCAGTTCTCCTGCCTCAGCCTCCAGAGTAGC TCGGCTCACTGCATCCTCCACCTTCCGGGCTCCAGCAGTTCTCCTGCCTCAGCCTCCAGAGTAGC A C FGFR1OP2 Ensembl:ENSG00000111790 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913421065 Functional Loss SNV dbSNP153 33..33 33 - - - 35644 RMVar_ID_35644 Human_SNP_ID_494693249 A-to-I Human chr12 - 26977702 26977702 26977702 TCTCCCAGGCTAGAGTGCAGTCGCGCAGTCTCAGTTCACTGCAACCTCCACCTCCCGAGTTCAAG TCTCCCAGGCTAGAGTGCAGTCGCGCAGTCTCTGTTCACTGCAACCTCCACCTCCCGAGTTCAAG T A TM7SF3 Ensembl:ENSG00000064115 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7309280 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_4042,GWAS_ID_4043 RMVar_hsa_circ_155432,RMVar_hsa_circ_91077,RMVar_hsa_circ_113847,RMVar_hsa_circ_123334,RMVar_hsa_circ_155433,RMVar_hsa_circ_155434,RMVar_hsa_circ_265575,RMVar_hsa_circ_155435,RMVar_hsa_circ_155436,RMVar_hsa_circ_266182,RMVar_hsa_circ_266379,RMVar_hsa_circ_51618 35645 RMVar_ID_35645 Human_SNP_ID_494693250 A-to-I Human chr12 - 26977702 26977702 26977702 TCTCCCAGGCTAGAGTGCAGTCGCGCAGTCTCAGTTCACTGCAACCTCCACCTCCCGAGTTCAAG TCTCCCAGGCTAGAGTGCAGTCGCGCAGTCTCGGTTCACTGCAACCTCCACCTCCCGAGTTCAAG T C TM7SF3 Ensembl:ENSG00000064115 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7309280 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_4042,GWAS_ID_4043 RMVar_hsa_circ_155432,RMVar_hsa_circ_91077,RMVar_hsa_circ_113847,RMVar_hsa_circ_123334,RMVar_hsa_circ_155433,RMVar_hsa_circ_155434,RMVar_hsa_circ_265575,RMVar_hsa_circ_155435,RMVar_hsa_circ_155436,RMVar_hsa_circ_266182,RMVar_hsa_circ_266379,RMVar_hsa_circ_51618 35646 RMVar_ID_35646 Human_SNP_ID_494693331 A-to-I Human chr12 - 26977926 26977926 26977926 ATGCCTGGTAAGCTTTTATTTTTAGTAGAGACAGAGTCTCACTGTTGCCTAGGGTGGTCTTAAAC ATGCCTGGTAAGCTTTTATTTTTAGTAGAGACGGAGTCTCACTGTTGCCTAGGGTGGTCTTAAAC T C TM7SF3 Ensembl:ENSG00000064115 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1401748684 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_155432,RMVar_hsa_circ_91077,RMVar_hsa_circ_113847,RMVar_hsa_circ_123334,RMVar_hsa_circ_155433,RMVar_hsa_circ_155434,RMVar_hsa_circ_265575,RMVar_hsa_circ_155435,RMVar_hsa_circ_155436,RMVar_hsa_circ_266182,RMVar_hsa_circ_266379,RMVar_hsa_circ_51618 35647 RMVar_ID_35647 Human_SNP_ID_494693356 A-to-I Human chr12 - 26978033 26978033 26978033 GGACTGCAGTGACACTATCATAGCTCACTGCAACCTCAAACTCTAAGGCTCAAGCCATCCTCTTA GGACTGCAGTGACACTATCATAGCTCACTGCAGCCTCAAACTCTAAGGCTCAAGCCATCCTCTTA T C TM7SF3 Ensembl:ENSG00000064115 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs183679708 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1349304,Human_Splice_Rec_1349305 RMVar_hsa_circ_155432,RMVar_hsa_circ_91077,RMVar_hsa_circ_113847,RMVar_hsa_circ_123334,RMVar_hsa_circ_155433,RMVar_hsa_circ_155434,RMVar_hsa_circ_265575,RMVar_hsa_circ_155435,RMVar_hsa_circ_155436,RMVar_hsa_circ_266182,RMVar_hsa_circ_266379,RMVar_hsa_circ_51618 35648 RMVar_ID_35648 Human_SNP_ID_494693363 A-to-I Human chr12 - 26978058 26978058 26978058 AGGATCTCTTTCTGTCACCCATGCTGGACTGCAGTGACACTATCATAGCTCACTGCAACCTCAAA AGGATCTCTTTCTGTCACCCATGCTGGACTGCGGTGACACTATCATAGCTCACTGCAACCTCAAA T C TM7SF3 Ensembl:ENSG00000064115 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1179839993 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11912918 Human_Splice_Rec_1349304 RMVar_hsa_circ_155432,RMVar_hsa_circ_91077,RMVar_hsa_circ_113847,RMVar_hsa_circ_123334,RMVar_hsa_circ_155433,RMVar_hsa_circ_155434,RMVar_hsa_circ_265575,RMVar_hsa_circ_155435,RMVar_hsa_circ_155436,RMVar_hsa_circ_266182,RMVar_hsa_circ_266379,RMVar_hsa_circ_51618 35649 RMVar_ID_35649 Human_SNP_ID_494693478 A-to-I Human chr12 - 26978706 26978706 26978706 AGGTGTTGTAGTGCACACCTGTGGTCTCAGCTACTCTGGGAGGCTGAGGCTAGAGGATTGCTTGA AGGTGTTGTAGTGCACACCTGTGGTCTCAGCTCCTCTGGGAGGCTGAGGCTAGAGGATTGCTTGA T G TM7SF3 Ensembl:ENSG00000064115 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1237148042 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_155432,RMVar_hsa_circ_91077,RMVar_hsa_circ_113847,RMVar_hsa_circ_123334,RMVar_hsa_circ_155433,RMVar_hsa_circ_155434,RMVar_hsa_circ_265575,RMVar_hsa_circ_155435,RMVar_hsa_circ_155436,RMVar_hsa_circ_266182,RMVar_hsa_circ_266379,RMVar_hsa_circ_51618 35650 RMVar_ID_35650 Human_SNP_ID_494695898 A-to-I Human chr12 - 26988420 26988420 26988420 GTGTCTCACGCCTGTAATCCCAGCACATTGGGAGGTCAAGATGGGCGGATTGCTTGAGCTCCAGA GTGTCTCACGCCTGTAATCCCAGCACATTGGGCGGTCAAGATGGGCGGATTGCTTGAGCTCCAGA T G TM7SF3 Ensembl:ENSG00000064115 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1032274126 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_155432,RMVar_hsa_circ_91077,RMVar_hsa_circ_123334,RMVar_hsa_circ_155433,RMVar_hsa_circ_155436,RMVar_hsa_circ_266379,RMVar_hsa_circ_304304,RMVar_hsa_circ_51618,RMVar_hsa_circ_378029,RMVar_hsa_circ_317415,RMVar_hsa_circ_278776,RMVar_hsa_circ_107534,RMVar_hsa_circ_155443,RMVar_hsa_circ_31992,RMVar_hsa_circ_155444,RMVar_hsa_circ_155445,RMVar_hsa_circ_155441,RMVar_hsa_circ_155442,RMVar_hsa_circ_65150,RMVar_hsa_circ_309042,RMVar_hsa_circ_292564,RMVar_hsa_circ_155449,RMVar_hsa_circ_276377,RMVar_hsa_circ_155446,RMVar_hsa_circ_155447,RMVar_hsa_circ_311457,RMVar_hsa_circ_313336,RMVar_hsa_circ_316275,RMVar_hsa_circ_281133,RMVar_hsa_circ_155451,RMVar_hsa_circ_155450,RMVar_hsa_circ_155448 35651 RMVar_ID_35651 Human_SNP_ID_494696109 A-to-I Human chr12 - 26989171 26989171 26989171 TTGGCCTCCCAAAGTGCTGGGATTACAGGCATAAGCCACCATACCCCACCCGTGTATAACTTTGA TTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCATACCCCACCCGTGTATAACTTTGA T C TM7SF3 Ensembl:ENSG00000064115 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1204686322 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_155432,RMVar_hsa_circ_91077,RMVar_hsa_circ_123334,RMVar_hsa_circ_155433,RMVar_hsa_circ_155436,RMVar_hsa_circ_266379,RMVar_hsa_circ_304304,RMVar_hsa_circ_51618,RMVar_hsa_circ_378029,RMVar_hsa_circ_317415,RMVar_hsa_circ_278776,RMVar_hsa_circ_107534,RMVar_hsa_circ_155443,RMVar_hsa_circ_31992,RMVar_hsa_circ_155444,RMVar_hsa_circ_155445,RMVar_hsa_circ_155441,RMVar_hsa_circ_155442,RMVar_hsa_circ_65150,RMVar_hsa_circ_309042,RMVar_hsa_circ_292564,RMVar_hsa_circ_155449,RMVar_hsa_circ_276377,RMVar_hsa_circ_155446,RMVar_hsa_circ_155447,RMVar_hsa_circ_311457,RMVar_hsa_circ_313336,RMVar_hsa_circ_316275,RMVar_hsa_circ_281133,RMVar_hsa_circ_155451,RMVar_hsa_circ_155450,RMVar_hsa_circ_155448 35652 RMVar_ID_35652 Human_SNP_ID_494707306 A-to-I Human chr12 + 27034516 27034516 27034516 TCTTCCAGGCTGCAGTGCAGTGACACAATCACAGTTCATTGCAGTGTTGACCTCCTGGGCTCAAG TCTTCCAGGCTGCAGTGCAGTGACACAATCACGGTTCATTGCAGTGTTGACCTCCTGGGCTCAAG A G MED21 Ensembl:ENSG00000152944 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1420989327 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_155464 35653 RMVar_ID_35653 Human_SNP_ID_494707351 A-to-I Human chr12 + 27034661 27034661 27034661 TGGGGTTTTGCAGTGTTGCCCAGGCTTATCTCAAACTCCTGGGCTCAACCGATCTGCCCATTTCG TGGGGTTTTGCAGTGTTGCCCAGGCTTATCTCCAACTCCTGGGCTCAACCGATCTGCCCATTTCG A C MED21 Ensembl:ENSG00000152944 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1287047517 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_155464 35654 RMVar_ID_35654 Human_SNP_ID_494707440 A-to-I Human chr12 + 27034940 27034940 27034940 GCCTGGCTAATTTTTGTATTTTTCGTAGAGACAGGGTTTTACCATGTTTACCAGGCTAGTCTTGA GCCTGGCTAATTTTTGTATTTTTCGTAGAGACCGGGTTTTACCATGTTTACCAGGCTAGTCTTGA A C MED21 Ensembl:ENSG00000152944 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1460789896 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11913566 RMVar_hsa_circ_155464 35655 RMVar_ID_35655 Human_SNP_ID_494707447 A-to-I Human chr12 + 27034965 27034965 27034965 TAGAGACAGGGTTTTACCATGTTTACCAGGCTAGTCTTGAATTCCTGACCTTAGGTGCTCCGCCT TAGAGACAGGGTTTTACCATGTTTACCAGGCTGGTCTTGAATTCCTGACCTTAGGTGCTCCGCCT A G MED21 Ensembl:ENSG00000152944 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229,31158229 RNA-Seq:(High) rs375346575 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11913567 RMVar_hsa_circ_155464 35656 RMVar_ID_35656 Human_SNP_ID_494708856 A-to-I Human chr12 + 27039910 27039910 27039910 CTGACCTTGTGATCTGCCCACCTCAGCTTCCCAAAGTGCTGGGATTACAGGCGTGAACTTTGATT CTGACCTTGTGATCTGCCCACCTCAGCTTCCCGAAGTGCTGGGATTACAGGCGTGAACTTTGATT A G MED21 Ensembl:ENSG00000152944 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909057965 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3402004 RMVar_hsa_circ_155464 35657 RMVar_ID_35657 Human_SNP_ID_494773107 A-to-I Human chr12 + 27313386 27313383 27313387 AAAGAATTCTGGGTTTTGTTTTGTTTTGTTTTAATTTTTATTTTTTGAGATGAAGTCTCGCTCTG AAAGAATTCTGGGTTTTGTTTTGTTTTGTT____TTTTTATTTTTTGAGATGAAGTCTCGCTCTG TTTAA T STK38L Ensembl:ENSG00000211455 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1433325342 Functional Loss DEL dbSNP153 31..34 33 - - - RMVar_hsa_circ_117233,RMVar_hsa_circ_155466,RMVar_hsa_circ_69788 35658 RMVar_ID_35658 Human_SNP_ID_494773121 A-to-I Human chr12 + 27313425 27313425 27313425 ATTTTTTGAGATGAAGTCTCGCTCTGTTGCCTAGGCTGGAGTGCAGTGGTGTGATCTTGGCTCAC ATTTTTTGAGATGAAGTCTCGCTCTGTTGCCTTGGCTGGAGTGCAGTGGTGTGATCTTGGCTCAC A T STK38L Ensembl:ENSG00000211455 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1250186783 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117233,RMVar_hsa_circ_155466,RMVar_hsa_circ_69788 35659 RMVar_ID_35659 Human_SNP_ID_494782395 A-to-I Human chr12 + 27354351 27354351 27354351 AGAAAACCAAATAGTGTATGTTCTCAGTTATTAGTGGGAGCTAAACACTGAGTACACATGGACAC AGAAAACCAAATAGTGTATGTTCTCAGTTATTCGTGGGAGCTAAACACTGAGTACACATGGACAC A C ARNTL2 Ensembl:ENSG00000029153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1036424027 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117233,RMVar_hsa_circ_155466,RMVar_hsa_circ_111023,RMVar_hsa_circ_155469 35660 RMVar_ID_35660 Human_SNP_ID_494798198 A-to-I Human chr12 + 27421384 27421383 27421384 CCTGGCCAATATGGTGAAACCCCGTTTCTACTAAAAATACAAAAAAAATTACCCAGGCACTCACT CCTGGCCAATATGGTGAAACCCCGTTTCTACT_AAAATACAAAAAAAATTACCCAGGCACTCACT TA T ARNTL2 Ensembl:ENSG00000029153 Protein coding 3'UTR GSE38233;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29796672,31158229,32596459 RNA-Seq:(High) rs34336841 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_117233,RMVar_hsa_circ_155466,RMVar_hsa_circ_155484,RMVar_hsa_circ_155491,RMVar_hsa_circ_155492 35661 RMVar_ID_35661 Human_SNP_ID_494798199 A-to-I Human chr12 - 27421383 27421383 27421383 GTGAGTGCCTGGGTAATTTTTTTTGTATTTTTAGTAGAAACGGGGTTTCACCATATTGGCCAGGC GTGAGTGCCTGGGTAATTTTTTTTGTATTTTTGGTAGAAACGGGGTTTCACCATATTGGCCAGGC T C ARNTL2-AS1 Ensembl:ENSG00000245311 lincRNA intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1227060052 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_117499 35662 RMVar_ID_35662 Human_SNP_ID_494798200 A-to-I Human chr12 + 27421390 27421390 27421390 CAATATGGTGAAACCCCGTTTCTACTAAAAATACAAAAAAAATTACCCAGGCACTCACTCTTGAG CAATATGGTGAAACCCCGTTTCTACTAAAAATCCAAAAAAAATTACCCAGGCACTCACTCTTGAG A C ARNTL2 Ensembl:ENSG00000029153 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs557649373 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117233,RMVar_hsa_circ_155466,RMVar_hsa_circ_155484,RMVar_hsa_circ_155491,RMVar_hsa_circ_155492 35663 RMVar_ID_35663 Human_SNP_ID_494798201 A-to-I Human chr12 + 27421390 27421390 27421390 CAATATGGTGAAACCCCGTTTCTACTAAAAATACAAAAAAAATTACCCAGGCACTCACTCTTGAG CAATATGGTGAAACCCCGTTTCTACTAAAAATTCAAAAAAAATTACCCAGGCACTCACTCTTGAG A T ARNTL2 Ensembl:ENSG00000029153 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs557649373 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117233,RMVar_hsa_circ_155466,RMVar_hsa_circ_155484,RMVar_hsa_circ_155491,RMVar_hsa_circ_155492 35664 RMVar_ID_35664 Human_SNP_ID_494798202 A-to-I Human chr12 + 27421392 27421391 27421392 ATATGGTGAAACCCCGTTTCTACTAAAAATACAAAAAAAATTACCCAGGCACTCACTCTTGAGGT ATATGGTGAAACCCCGTTTCTACTAAAAATAC_AAAAAAATTACCCAGGCACTCACTCTTGAGGT CA C ARNTL2 Ensembl:ENSG00000029153 Protein coding 3'UTR GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs752772526 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_117233,RMVar_hsa_circ_155466,RMVar_hsa_circ_155484,RMVar_hsa_circ_155491,RMVar_hsa_circ_155492 35665 RMVar_ID_35665 Human_SNP_ID_494798222 A-to-I Human chr12 + 27421492 27421492 27421492 ATGAGCGCAAAGGCCTCATGACCTAATGGCACACACCTGTAATCCCAACTGCTTGGGAGGCTGAG ATGAGCGCAAAGGCCTCATGACCTAATGGCACGCACCTGTAATCCCAACTGCTTGGGAGGCTGAG A G ARNTL2 Ensembl:ENSG00000029153 Protein coding 3'UTR GSE38233;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,32596459 RNA-Seq:(High) rs1440061235 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117233,RMVar_hsa_circ_155466,RMVar_hsa_circ_155484,RMVar_hsa_circ_155491,RMVar_hsa_circ_155492 35666 RMVar_ID_35666 Human_SNP_ID_494798225 A-to-I Human chr12 + 27421500 27421500 27421500 AAAGGCCTCATGACCTAATGGCACACACCTGTAATCCCAACTGCTTGGGAGGCTGAGGCGAGAGG AAAGGCCTCATGACCTAATGGCACACACCTGTGATCCCAACTGCTTGGGAGGCTGAGGCGAGAGG A G ARNTL2 Ensembl:ENSG00000029153 Protein coding 3'UTR GSE38233;GSE100210;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,29129909,29796672,31158229 RNA-Seq:(High) rs113632419 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117233,RMVar_hsa_circ_155466,RMVar_hsa_circ_155484,RMVar_hsa_circ_155491,RMVar_hsa_circ_155492 35667 RMVar_ID_35667 Human_SNP_ID_494798241 A-to-I Human chr12 + 27421578 27421578 27421578 GGGAGGCAGAGGTTGCAGTGAGCCGAGATCGCACCACTGCACTCCAGTCTGGGCAACAGAGTGAG GGGAGGCAGAGGTTGCAGTGAGCCGAGATCGCGCCACTGCACTCCAGTCTGGGCAACAGAGTGAG A G ARNTL2 Ensembl:ENSG00000029153 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1392801086 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117233,RMVar_hsa_circ_155466,RMVar_hsa_circ_155484,RMVar_hsa_circ_155491,RMVar_hsa_circ_155492 35668 RMVar_ID_35668 Human_SNP_ID_494798669 A-to-I Human chr12 + 27423349 27423349 27423349 TTCTTTTCTTTTTTTTTTTTTTTTTTTTTTTGAGATGGAGTCTCGCTCTATCGCCCAGGCTGGAG TTCTTTTCTTTTTTTTTTTTTTTTTTTTTTTGGGATGGAGTCTCGCTCTATCGCCCAGGCTGGAG A G ARNTL2 Ensembl:ENSG00000029153 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1437094985 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117233,RMVar_hsa_circ_155466,RMVar_hsa_circ_155484,RMVar_hsa_circ_155491,RMVar_hsa_circ_155492 35669 RMVar_ID_35669 Human_SNP_ID_494798670 A-to-I Human chr12 + 27423349 27423349 27423349 TTCTTTTCTTTTTTTTTTTTTTTTTTTTTTTGAGATGGAGTCTCGCTCTATCGCCCAGGCTGGAG TTCTTTTCTTTTTTTTTTTTTTTTTTTTTTTGTGATGGAGTCTCGCTCTATCGCCCAGGCTGGAG A T ARNTL2 Ensembl:ENSG00000029153 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1437094985 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117233,RMVar_hsa_circ_155466,RMVar_hsa_circ_155484,RMVar_hsa_circ_155491,RMVar_hsa_circ_155492 35670 RMVar_ID_35670 Human_SNP_ID_494798679 A-to-I Human chr12 + 27423366 27423366 27423366 TTTTTTTTTTTTTTGAGATGGAGTCTCGCTCTATCGCCCAGGCTGGAGTGCAGTGGCGCGATCTT TTTTTTTTTTTTTTGAGATGGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCGATCTT A G ARNTL2 Ensembl:ENSG00000029153 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,31158229,31158229,31158229 RNA-Seq:(High) rs1276643315 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117233,RMVar_hsa_circ_155466,RMVar_hsa_circ_155484,RMVar_hsa_circ_155491,RMVar_hsa_circ_155492 35671 RMVar_ID_35671 Human_SNP_ID_494798692 A-to-I Human chr12 + 27423404 27423404 27423404 CAGGCTGGAGTGCAGTGGCGCGATCTTGGCTCACTGCCATCTCTGCCTCCTGGGTTCACGCCATT CAGGCTGGAGTGCAGTGGCGCGATCTTGGCTCGCTGCCATCTCTGCCTCCTGGGTTCACGCCATT A G ARNTL2 Ensembl:ENSG00000029153 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1189591276 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117233,RMVar_hsa_circ_155466,RMVar_hsa_circ_155484,RMVar_hsa_circ_155491,RMVar_hsa_circ_155492 35672 RMVar_ID_35672 Human_SNP_ID_494798702 A-to-I Human chr12 + 27423466 27423466 27423466 ATTCTGCCTCAGCCTCCAGAGCAGCTGGGACCACAGGCGCCCGCCACCACACCTGGCTAATTTTG ATTCTGCCTCAGCCTCCAGAGCAGCTGGGACCGCAGGCGCCCGCCACCACACCTGGCTAATTTTG A G ARNTL2 Ensembl:ENSG00000029153 Protein coding 3'UTR GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1482164706 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_417572 RMVar_hsa_circ_117233,RMVar_hsa_circ_155466,RMVar_hsa_circ_155484,RMVar_hsa_circ_155491,RMVar_hsa_circ_155492 35673 RMVar_ID_35673 Human_SNP_ID_494798742 A-to-I Human chr12 + 27423589 27423589 27423589 CTGACCTCGTGATCCGCCCACTTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGCG CTGACCTCGTGATCCGCCCACTTCGGCCTCCCCAAGTGCTGGGATTACAGGCATGAGCCACTGCG A C ARNTL2 Ensembl:ENSG00000029153 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs1437908913 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117233,RMVar_hsa_circ_155466,RMVar_hsa_circ_155484,RMVar_hsa_circ_155491,RMVar_hsa_circ_155492 35674 RMVar_ID_35674 Human_SNP_ID_494798743 A-to-I Human chr12 + 27423590 27423590 27423590 TGACCTCGTGATCCGCCCACTTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGCGC TGACCTCGTGATCCGCCCACTTCGGCCTCCCAGAGTGCTGGGATTACAGGCATGAGCCACTGCGC A G ARNTL2 Ensembl:ENSG00000029153 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,31158229,31158229,31158229 RNA-Seq:(High) rs952137925 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117233,RMVar_hsa_circ_155466,RMVar_hsa_circ_155484,RMVar_hsa_circ_155491,RMVar_hsa_circ_155492 35675 RMVar_ID_35675 Human_SNP_ID_494798745 A-to-I Human chr12 + 27423609 27423609 27423609 CTTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGCGCCCGGCCTACTCTACACTTT CTTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCGCCCGGCCTACTCTACACTTT A G ARNTL2 Ensembl:ENSG00000029153 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,31158229,32596459 RNA-Seq:(High) rs1016724606 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117233,RMVar_hsa_circ_155466,RMVar_hsa_circ_155484,RMVar_hsa_circ_155491,RMVar_hsa_circ_155492 35676 RMVar_ID_35676 Human_SNP_ID_494858042 A-to-I Human chr12 + 27684872 27684872 27684872 TGTATACCTTTCACTCAGCTTCCTCTAACGTTAACATCTTACGTAATCATGATTACATTCATCAA TGTATACCTTTCACTCAGCTTCCTCTAACGTTGACATCTTACGTAATCATGATTACATTCATCAA A G PPFIBP1 Ensembl:ENSG00000110841 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1351934566 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_331584,RMVar_hsa_circ_96140,RMVar_hsa_circ_112274,RMVar_hsa_circ_155502,RMVar_hsa_circ_155503,RMVar_hsa_circ_29253,RMVar_hsa_circ_291487,RMVar_hsa_circ_373775,RMVar_hsa_circ_289534,RMVar_hsa_circ_155508,RMVar_hsa_circ_58403,RMVar_hsa_circ_328197,RMVar_hsa_circ_32869,RMVar_hsa_circ_155510 35677 RMVar_ID_35677 Human_SNP_ID_494860085 A-to-I Human chr12 + 27693635 27693635 27693635 ACCACAAAATTGTTGAACAGTTTAAGAATTTCAACCTTAATCTTGGATCCCTTTACCTCATATGG ACCACAAAATTGTTGAACAGTTTAAGAATTTCGACCTTAATCTTGGATCCCTTTACCTCATATGG A G PPFIBP1 Ensembl:ENSG00000110841 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs565529633 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1166356 RMVar_hsa_circ_96140,RMVar_hsa_circ_112274,RMVar_hsa_circ_155502,RMVar_hsa_circ_155503 35678 RMVar_ID_35678 Human_SNP_ID_494860216 A-to-I Human chr12 + 27694234 27694234 27694234 CAGGGTCTCACCATGTTGTCCAGCCTGGTCTCAAACTCCTGTCCTCAAGTGATCCTCCCACCTCA CAGGGTCTCACCATGTTGTCCAGCCTGGTCTCGAACTCCTGTCCTCAAGTGATCCTCCCACCTCA A G PPFIBP1 Ensembl:ENSG00000110841 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs918707284 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6170469 Human_miRNA_ID_1962253 RMVar_hsa_circ_96140,RMVar_hsa_circ_112274,RMVar_hsa_circ_155502,RMVar_hsa_circ_155503 35679 RMVar_ID_35679 Human_SNP_ID_494873318 A-to-I Human chr12 + 27751028 27751028 27751028 GGGGGGCTGAGGCGGGAGAATTGCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGACGAGATCATG GGGGGGCTGAGGCGGGAGAATTGCTTGAACCCGGGAGGCGGAGGTTGCAGTGAGACGAGATCATG A G MRPS35 Ensembl:ENSG00000061794 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1228210386 Functional Loss SNV dbSNP153 33..33 33 - - - 35680 RMVar_ID_35680 Human_SNP_ID_494883702 A-to-I Human chr12 + 27793432 27793294 27793432 GGTTGTGGTGGCATGTACCTGTAGTCCCAGTTACTTGGGAGGCTGAGACAGGAGGATTGCTTGAG _________________________________CTTGGGAGGCTGAGACAGGAGGATTGCTTGAG GCTTGGGAGGCTGAGGCAGGAGGATCACTTGAGCCTGGGTGTTCAAGATAGGCCTGGTCAACACAGCAAGACCCCTTCTCTAAAAATGAAAATAAAAAAATTAGCTGGTTGTGGTGGCATGTACCTGTAGTCCCAGTTA G KLHL42 Ensembl:ENSG00000087448 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1565484068 Functional Loss DEL dbSNP153 1..33 33 - - - Human_RBP_ID_17561065 RMVar_hsa_circ_116025,RMVar_hsa_circ_155521 35681 RMVar_ID_35681 Human_SNP_ID_494883719 A-to-I Human chr12 + 27793358 27793358 27793358 GCCTGGGTGTTCAAGATAGGCCTGGTCAACACAGCAAGACCCCTTCTCTAAAAATGAAAATAAAA GCCTGGGTGTTCAAGATAGGCCTGGTCAACACGGCAAGACCCCTTCTCTAAAAATGAAAATAAAA A G KLHL42 Ensembl:ENSG00000087448 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1013748562 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116025,RMVar_hsa_circ_155521 35682 RMVar_ID_35682 Human_SNP_ID_495031496 A-to-I Human chr12 + 28441752 28441749 28441752 TATATATCATATATCTCATATATATATCTCATATATATATGTATATGTGTATGCATGTGATATAT TATATATCATATATCTCATATATATATCTC___TATATATGTATATGTGTATGCATGTGATATAT CATA C CCDC91 Ensembl:ENSG00000123106 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1003733962 Functional Loss DEL dbSNP153 31..33 33 - - - 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_61899 35683 RMVar_ID_35683 Human_SNP_ID_495031499 A-to-I Human chr12 + 28441752 28441751 28441752 TATATATCATATATCTCATATATATATCTCATATATATATGTATATGTGTATGCATGTGATATAT TATATATCATATATCTCATATATATATCTCAT_TATATATGTATATGTGTATGCATGTGATATAT TA T CCDC91 Ensembl:ENSG00000123106 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1184045759 Functional Loss DEL dbSNP153 33..33 33 - - - 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_61899 35684 RMVar_ID_35684 Human_SNP_ID_495031503 A-to-I Human chr12 + 28441756 28441756 28441756 TATCATATATCTCATATATATATCTCATATATATATGTATATGTGTATGCATGTGATATATGGTC TATCATATATCTCATATATATATCTCATATATGTATGTATATGTGTATGCATGTGATATATGGTC A G CCDC91 Ensembl:ENSG00000123106 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1035833204 Functional Loss SNV dbSNP153 33..33 33 - - - 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_61899 35685 RMVar_ID_35685 Human_SNP_ID_495031504 A-to-I Human chr12 + 28441758 28441758 28441758 TCATATATCTCATATATATATCTCATATATATATGTATATGTGTATGCATGTGATATATGGTCAG TCATATATCTCATATATATATCTCATATATATGTGTATATGTGTATGCATGTGATATATGGTCAG A G CCDC91 Ensembl:ENSG00000123106 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs564083212 Functional Loss SNV dbSNP153 33..33 33 - - - 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_61899 35686 RMVar_ID_35686 Human_SNP_ID_495331823 A-to-I Human chr12 - 29668717 29668717 29668717 GTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGTGGATCACCTGAGGTCAGGA GTGGCTCATGCCTGTAATCCCAGCACTTTGGGGGGCCAAGGTGGGTGGATCACCTGAGGTCAGGA T C TMTC1 Ensembl:ENSG00000133687 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1051541249 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92363,RMVar_hsa_circ_155575,RMVar_hsa_circ_124458,RMVar_hsa_circ_36543,RMVar_hsa_circ_155578,RMVar_hsa_circ_41734,RMVar_hsa_circ_80318,RMVar_hsa_circ_155583,RMVar_hsa_circ_373915,RMVar_hsa_circ_155585,RMVar_hsa_circ_32017,RMVar_hsa_circ_273363,RMVar_hsa_circ_155588,RMVar_hsa_circ_1762,RMVar_hsa_circ_293119,RMVar_hsa_circ_330738,RMVar_hsa_circ_372164,RMVar_hsa_circ_155592,RMVar_hsa_circ_155594,RMVar_hsa_circ_155595,RMVar_hsa_circ_155593 35687 RMVar_ID_35687 Human_SNP_ID_606446562 A-to-I Human chr16 - 66546980 66546979 66546981 GGGAGGCAAAGGTGGGAGGATTGCTTGAGCTCAGGAGTCTGAGACCAGCCTGGGCAACATGGCAA GGGAGGCAAAGGTGGGAGGATTGCTTGAGCT__GGAGTCTGAGACCAGCCTGGGCAACATGGCAA CTG C TK2 Ensembl:ENSG00000166548 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs766512421 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_19806,RMVar_hsa_circ_21481,RMVar_hsa_circ_28034,RMVar_hsa_circ_70458 35688 RMVar_ID_35688 Human_SNP_ID_606446563 A-to-I Human chr16 - 66546980 66546979 66546980 GGGAGGCAAAGGTGGGAGGATTGCTTGAGCTCAGGAGTCTGAGACCAGCCTGGGCAACATGGCAA GGGAGGCAAAGGTGGGAGGATTGCTTGAGCTC_GGAGTCTGAGACCAGCCTGGGCAACATGGCAA CT C TK2 Ensembl:ENSG00000166548 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1364680395 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_19806,RMVar_hsa_circ_21481,RMVar_hsa_circ_28034,RMVar_hsa_circ_70458 35689 RMVar_ID_35689 Human_SNP_ID_606448948 A-to-I Human chr16 + 66555152 66555141 66555152 TCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTGGAACCGGAGAGACAGAGGTTGAGGTAAGC TCAGCTACTCGGGAGGCTGAGG___________CTGGAACCGGAGAGACAGAGGTTGAGGTAAGC GCAGGAGAATCA G CKLF-CMTM1,CKLF Ensembl:ENSG00000254788,Ensembl:ENSG00000217555 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1352094251 Functional Loss DEL dbSNP153 23..33 33 - - - 35690 RMVar_ID_35690 Human_SNP_ID_606477777 A-to-I Human chr16 - 66675998 66675998 66675998 TTTTTTAGCTGGGCATGGTGGCATGTGCTTATAGTTCCAGTTCCTTGGGTGGCAGAGGCGGGAAG TTTTTTAGCTGGGCATGGTGGCATGTGCTTATTGTTCCAGTTCCTTGGGTGGCAGAGGCGGGAAG T A CMTM4 Ensembl:ENSG00000183723 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1436860164 Functional Loss SNV dbSNP153 33..33 33 - - - 35691 RMVar_ID_35691 Human_SNP_ID_606481858 A-to-I Human chr16 - 66691619 66691619 66691619 ATAGGTTACTGCAGCCTCGACCTCCTGGGCTCAGGTGATCCTTCCACCTCAGCCCTCCAACTAGC ATAGGTTACTGCAGCCTCGACCTCCTGGGCTCGGGTGATCCTTCCACCTCAGCCCTCCAACTAGC T C CMTM4 Ensembl:ENSG00000183723 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037234514 Functional Loss SNV dbSNP153 33..33 33 - - - 35692 RMVar_ID_35692 Human_SNP_ID_606489471 A-to-I Human chr16 - 66721463 66721463 66721463 TGGAACCAAAGGCCAAATAATAAACAGCCTTTAGTTTTTAAAGTAAAATTCATTTTATTTGCAGA TGGAACCAAAGGCCAAATAATAAACAGCCTTTGGTTTTTAAAGTAAAATTCATTTTATTTGCAGA T C DYNC1LI2 Ensembl:ENSG00000135720 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1199661804 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6525300,Human_RBP_ID_8187798,Human_RBP_ID_12770876,Human_RBP_ID_17879086,Human_RBP_ID_22388864,Human_RBP_ID_23695202,Human_RBP_ID_26442362,Human_RBP_ID_27659539 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 35693 RMVar_ID_35693 Human_SNP_ID_606490805 A-to-I Human chr16 - 66726971 66726971 66726971 TGAGGCTGCAGTTGAGCTGTGATTATGCCACCATGCTCCAGCCAGGGTGACAGAGTGAGAGACTG TGAGGCTGCAGTTGAGCTGTGATTATGCCACCGTGCTCCAGCCAGGGTGACAGAGTGAGAGACTG T C DYNC1LI2 Ensembl:ENSG00000135720 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1340219652 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12771134,Human_RBP_ID_25219290 RMVar_hsa_circ_124215,RMVar_hsa_circ_108594,RMVar_hsa_circ_113583,RMVar_hsa_circ_103998,RMVar_hsa_circ_49120,RMVar_hsa_circ_178957,RMVar_hsa_circ_86225,RMVar_hsa_circ_93341,RMVar_hsa_circ_178959,RMVar_hsa_circ_178960,RMVar_hsa_circ_178958,RMVar_hsa_circ_178955,RMVar_hsa_circ_178956,RMVar_hsa_circ_294016,RMVar_hsa_circ_30777,RMVar_hsa_circ_41711,RMVar_hsa_circ_178963 35694 RMVar_ID_35694 Human_SNP_ID_606491317 A-to-I Human chr16 - 66729085 66729084 66729086 ATGTATGTTGTTTCACAGCTGGTCCACGACAAAGAGTTGGCAGCAGAAGATGAGCAGGTGTTCCT ATGTATGTTGTTTCACAGCTGGTCCACGACA__GAGTTGGCAGCAGAAGATGAGCAGGTGTTCCT CTT C DYNC1LI2 Ensembl:ENSG00000135720 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1351600477 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_44784,Human_RBP_ID_895442,Human_RBP_ID_2479024,Human_RBP_ID_9372917,Human_RBP_ID_12771224,Human_RBP_ID_18983881,Human_RBP_ID_27811876 Human_Splice_Rec_1723772,Human_Splice_Rec_1723773,Human_Splice_Rec_1723794,Human_Splice_Rec_1723795,Human_Splice_Rec_1723803,Human_Splice_Rec_1723808,Human_Splice_Rec_1723809,Human_Splice_Rec_1723824,Human_Splice_Rec_1723825,Human_Splice_Rec_1723840,Human_Splice_Rec_1723841,Human_Splice_Rec_1723854,Human_Splice_Rec_1723855,Human_Splice_Rec_1723860 RMVar_hsa_circ_124215,RMVar_hsa_circ_108594,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_178959,RMVar_hsa_circ_178958,RMVar_hsa_circ_178955,RMVar_hsa_circ_178956,RMVar_hsa_circ_294016,RMVar_hsa_circ_49799,RMVar_hsa_circ_30777,RMVar_hsa_circ_109490,RMVar_hsa_circ_178963,RMVar_hsa_circ_279756,RMVar_hsa_circ_178965,RMVar_hsa_circ_178967,RMVar_hsa_circ_25272,RMVar_hsa_circ_178966,RMVar_hsa_circ_178964,RMVar_hsa_circ_67167,RMVar_hsa_circ_319145 35695 RMVar_ID_35695 Human_SNP_ID_606493909 A-to-I Human chr16 - 66738658 66738658 66738658 GTTGGCCAGGCTGGTCTTGAATTCCTGACCTCATGATCCACCCGCCTTGGCCTGCCACAGTTCTG GTTGGCCAGGCTGGTCTTGAATTCCTGACCTCGTGATCCACCCGCCTTGGCCTGCCACAGTTCTG T C DYNC1LI2 Ensembl:ENSG00000135720 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1184206703 Functional Loss SNV dbSNP153 33..33 33 - - - 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_178969,RMVar_hsa_circ_319145,RMVar_hsa_circ_316889,RMVar_hsa_circ_23453,RMVar_hsa_circ_78309,RMVar_hsa_circ_88939,RMVar_hsa_circ_178968,RMVar_hsa_circ_178973,RMVar_hsa_circ_178976,RMVar_hsa_circ_178974,RMVar_hsa_circ_320321,RMVar_hsa_circ_296572 35696 RMVar_ID_35696 Human_SNP_ID_606495611 A-to-I Human chr16 - 66745117 66745117 66745117 ATCACCACAGGTCAGGAGTTCGAGACTAGCCCAGCCAACATGGTGAAACCCGGTCTCTACTAAAA ATCACCACAGGTCAGGAGTTCGAGACTAGCCCGGCCAACATGGTGAAACCCGGTCTCTACTAAAA T C DYNC1LI2 Ensembl:ENSG00000135720 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1389817204 Functional Loss SNV dbSNP153 33..33 33 - - - 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 35697 RMVar_ID_35697 Human_SNP_ID_606495680 A-to-I Human chr16 - 66745411 66745411 66745411 CAGCCAGTATGGTGGCACACAACTGTAATCCCAGCCACTCAAGAGCCTGAGGCATGAGGATCGCC CAGCCAGTATGGTGGCACACAACTGTAATCCCGGCCACTCAAGAGCCTGAGGCATGAGGATCGCC T C DYNC1LI2 Ensembl:ENSG00000135720 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1338991944 Functional Loss SNV dbSNP153 33..33 33 - - - 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 35698 RMVar_ID_35698 Human_SNP_ID_606495780 A-to-I Human chr16 - 66745804 66745804 66745804 CACCTCCCGAGCTCGAGCAGTCCTCCCTCCTCAGTCTCCCGAGTAGCTGGGACTACAGGTACATG CACCTCCCGAGCTCGAGCAGTCCTCCCTCCTCGGTCTCCCGAGTAGCTGGGACTACAGGTACATG T C DYNC1LI2 Ensembl:ENSG00000135720 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1430523256 Functional Loss SNV dbSNP153 33..33 33 - - - 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 35699 RMVar_ID_35699 Human_SNP_ID_606496304 A-to-I Human chr16 - 66747790 66747790 66747790 GAGGCGGGTGGATCACTTGGGATCAGGAGTTCAAGACCAGCCTGGTCAACTTGGTGAAACCCCAT GAGGCGGGTGGATCACTTGGGATCAGGAGTTCCAGACCAGCCTGGTCAACTTGGTGAAACCCCAT T G DYNC1LI2 Ensembl:ENSG00000135720 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1258633721 Functional Loss SNV dbSNP153 33..33 33 - - - 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 35700 RMVar_ID_35700 Human_SNP_ID_606496405 A-to-I Human chr16 - 66748170 66748170 66748170 AGCCTCGGGTCATCCTTCCACCTCATCCTCCTAAGCAGCTGGGACTATAGATGTGTGCCACCACA AGCCTCGGGTCATCCTTCCACCTCATCCTCCTGAGCAGCTGGGACTATAGATGTGTGCCACCACA T C DYNC1LI2 Ensembl:ENSG00000135720 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs576822457 Functional Loss SNV dbSNP153 33..33 33 - - - 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 35701 RMVar_ID_35701 Human_SNP_ID_606496414 A-to-I Human chr16 - 66748231 66748231 66748231 CTCTGTCACCCAGGCTGGGGTGCAGTGGCTCAATCTTGGCTCATTGCAACCTCTGCCTCCCAGCC CTCTGTCACCCAGGCTGGGGTGCAGTGGCTCAGTCTTGGCTCATTGCAACCTCTGCCTCCCAGCC T C DYNC1LI2 Ensembl:ENSG00000135720 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1257081141 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22715357 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 35702 RMVar_ID_35702 Human_SNP_ID_606510548 A-to-I Human chr16 - 66806492 66806492 66806492 TGAACCCGGCAGGCAGAGGTTGCGGTGAGCCGAGACTGCACCACTGCACTCCAGCCTAGGTAACA TGAACCCGGCAGGCAGAGGTTGCGGTGAGCCGGGACTGCACCACTGCACTCCAGCCTAGGTAACA T C NAE1 Ensembl:ENSG00000159593 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs979146512 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45740,RMVar_hsa_circ_4721,RMVar_hsa_circ_178979,RMVar_hsa_circ_90509,RMVar_hsa_circ_298337,RMVar_hsa_circ_316840,RMVar_hsa_circ_178980,RMVar_hsa_circ_178981,RMVar_hsa_circ_107419,RMVar_hsa_circ_325455,RMVar_hsa_circ_178983 35703 RMVar_ID_35703 Human_SNP_ID_606510777 A-to-I Human chr16 - 66807422 66807422 66807422 TTGGCCAGGCTGGTCTCGAACTCCTGACCTCAAGTGATCCTCCTGTGTTGGCCTCCCAAAGTGCA TTGGCCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCCTCCTGTGTTGGCCTCCCAAAGTGCA T C NAE1 Ensembl:ENSG00000159593 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1278905335 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45740,RMVar_hsa_circ_4721,RMVar_hsa_circ_178979,RMVar_hsa_circ_90509,RMVar_hsa_circ_298337,RMVar_hsa_circ_316840,RMVar_hsa_circ_178980,RMVar_hsa_circ_178981,RMVar_hsa_circ_107419,RMVar_hsa_circ_325455,RMVar_hsa_circ_178983 35704 RMVar_ID_35704 Human_SNP_ID_606515042 A-to-I Human chr16 - 66823778 66823778 66823778 GCAGTGAGCTATGATCAGGCCACTATGCTACAAACTGGGCAACAGAGCAAAAGCCTGTCTCTAAA GCAGTGAGCTATGATCAGGCCACTATGCTACATACTGGGCAACAGAGCAAAAGCCTGTCTCTAAA T A NAE1 Ensembl:ENSG00000159593 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs967606802 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25219745 RMVar_hsa_circ_3610,RMVar_hsa_circ_45740,RMVar_hsa_circ_178979,RMVar_hsa_circ_90509,RMVar_hsa_circ_113479,RMVar_hsa_circ_178986,RMVar_hsa_circ_324245,RMVar_hsa_circ_341112,RMVar_hsa_circ_178988,RMVar_hsa_circ_29969,RMVar_hsa_circ_339402,RMVar_hsa_circ_348414,RMVar_hsa_circ_178991,RMVar_hsa_circ_178990,RMVar_hsa_circ_269701,RMVar_hsa_circ_318033,RMVar_hsa_circ_20758,RMVar_hsa_circ_353708,RMVar_hsa_circ_12717,RMVar_hsa_circ_50534,RMVar_hsa_circ_42293 35705 RMVar_ID_35705 Human_SNP_ID_606515054 A-to-I Human chr16 - 66823824 66823824 66823824 GGGAGGCTGAGGCAGGAAGATTGCTTAAGCCTAGGAGTTCAAGGCTGCAGTGAGCTATGATCAGG GGGAGGCTGAGGCAGGAAGATTGCTTAAGCCTGGGAGTTCAAGGCTGCAGTGAGCTATGATCAGG T C NAE1 Ensembl:ENSG00000159593 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1361662027 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3610,RMVar_hsa_circ_45740,RMVar_hsa_circ_178979,RMVar_hsa_circ_90509,RMVar_hsa_circ_113479,RMVar_hsa_circ_178986,RMVar_hsa_circ_324245,RMVar_hsa_circ_341112,RMVar_hsa_circ_178988,RMVar_hsa_circ_29969,RMVar_hsa_circ_339402,RMVar_hsa_circ_348414,RMVar_hsa_circ_178991,RMVar_hsa_circ_178990,RMVar_hsa_circ_269701,RMVar_hsa_circ_318033,RMVar_hsa_circ_20758,RMVar_hsa_circ_353708,RMVar_hsa_circ_12717,RMVar_hsa_circ_50534,RMVar_hsa_circ_42293 35706 RMVar_ID_35706 Human_SNP_ID_606515175 A-to-I Human chr16 - 66824358 66824358 66824358 TCGATCTCCTGACCTTGTGATCCACCCGCTTCAGCCTCCCAAAGTGCTGAGATTACAGGCATGAG TCGATCTCCTGACCTTGTGATCCACCCGCTTCGGCCTCCCAAAGTGCTGAGATTACAGGCATGAG T C NAE1 Ensembl:ENSG00000159593 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1376594911 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3610,RMVar_hsa_circ_45740,RMVar_hsa_circ_178979,RMVar_hsa_circ_90509,RMVar_hsa_circ_113479,RMVar_hsa_circ_178986,RMVar_hsa_circ_324245,RMVar_hsa_circ_341112,RMVar_hsa_circ_178988,RMVar_hsa_circ_29969,RMVar_hsa_circ_339402,RMVar_hsa_circ_348414,RMVar_hsa_circ_178991,RMVar_hsa_circ_178990,RMVar_hsa_circ_269701,RMVar_hsa_circ_318033,RMVar_hsa_circ_20758,RMVar_hsa_circ_353708,RMVar_hsa_circ_12717,RMVar_hsa_circ_50534,RMVar_hsa_circ_42293 35707 RMVar_ID_35707 Human_SNP_ID_606515209 A-to-I Human chr16 - 66824480 66824480 66824480 TCACGCCGTTCTCCTCCCTCAGTCTTCCGAGTAGCTGAGACTACAGGCGCCCACCACCACGCCTG TCACGCCGTTCTCCTCCCTCAGTCTTCCGAGTTGCTGAGACTACAGGCGCCCACCACCACGCCTG T A NAE1 Ensembl:ENSG00000159593 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1424666920 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3610,RMVar_hsa_circ_45740,RMVar_hsa_circ_178979,RMVar_hsa_circ_90509,RMVar_hsa_circ_113479,RMVar_hsa_circ_178986,RMVar_hsa_circ_324245,RMVar_hsa_circ_341112,RMVar_hsa_circ_178988,RMVar_hsa_circ_29969,RMVar_hsa_circ_339402,RMVar_hsa_circ_348414,RMVar_hsa_circ_178991,RMVar_hsa_circ_178990,RMVar_hsa_circ_269701,RMVar_hsa_circ_318033,RMVar_hsa_circ_20758,RMVar_hsa_circ_353708,RMVar_hsa_circ_12717,RMVar_hsa_circ_50534,RMVar_hsa_circ_42293 35708 RMVar_ID_35708 Human_SNP_ID_606531542 A-to-I Human chr16 + 66889867 66889867 66889867 CTGTAGTCTCAGCTGCTTGGAAGGCTGAAATGAGAGGATCTCTTGAGCCCAGGAGGTCTAGGCCA CTGTAGTCTCAGCTGCTTGGAAGGCTGAAATGGGAGGATCTCTTGAGCCCAGGAGGTCTAGGCCA A G PDP2 Ensembl:ENSG00000172840 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs905121353 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90756,RMVar_hsa_circ_178998 35709 RMVar_ID_35709 Human_SNP_ID_606531617 A-to-I Human chr16 + 66890205 66890205 66890205 GTGAGGCTGAGGCAGGAGAATCCCTTGAACCCAGAAGGCAGAGGTTGCAGTGAGCTGAGATTGTG GTGAGGCTGAGGCAGGAGAATCCCTTGAACCCCGAAGGCAGAGGTTGCAGTGAGCTGAGATTGTG A C PDP2 Ensembl:ENSG00000172840 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs965817993 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90756,RMVar_hsa_circ_178998 35710 RMVar_ID_35710 Human_SNP_ID_606543469 A-to-I Human chr16 - 66933153 66933152 66933153 GAAATCTCATCTCTACTAAAAATACAAAAATTAGTGGGGCGTGGTGGTGTGTGCCTGTGGTCCCA GAAATCTCATCTCTACTAAAAATACAAAAATT_GTGGGGCGTGGTGGTGTGTGCCTGTGGTCCCA CT C CIAO2B Ensembl:ENSG00000166595 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs760656299 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_103379,RMVar_hsa_circ_107703,RMVar_hsa_circ_94109,RMVar_hsa_circ_179001,RMVar_hsa_circ_179003,RMVar_hsa_circ_179002 35711 RMVar_ID_35711 Human_SNP_ID_606547041 A-to-I Human chr16 + 66944837 66944837 66944837 TGCCATGGGTCCTCTCTTGCTAGACACACTCCATAGATCCCCCCACTGAGCTGTGGATGGGCAAA TGCCATGGGTCCTCTCTTGCTAGACACACTCCGTAGATCCCCCCACTGAGCTGTGGATGGGCAAA A G AC009084.1,CES2 Ensembl:ENSG00000265408,Ensembl:ENSG00000172831 lincRNA,Protein coding intron,3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1457089119 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4377058,Human_RBP_ID_5181340,Human_RBP_ID_8188373,Human_RBP_ID_18286508,Human_RBP_ID_26810451 Human_miRNA_ID_1960880,Human_miRNA_ID_2653519,Human_miRNA_ID_2754717 RMVar_hsa_circ_112490,RMVar_hsa_circ_179010 35712 RMVar_ID_35712 Human_SNP_ID_606551130 A-to-I Human chr16 + 66961761 66961761 66961761 AATTTTTGTATTTTTAGGAGAGATGGGGTTTCACCATGTGGGCCAGGCTGGTCTCAAACTCCTGA AATTTTTGTATTTTTAGGAGAGATGGGGTTTCGCCATGTGGGCCAGGCTGGTCTCAAACTCCTGA A G AC009084.1,CES3 Ensembl:ENSG00000265408,Ensembl:ENSG00000172828 lincRNA,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1461112529 Functional Loss SNV dbSNP153 33..33 33 - - - 35713 RMVar_ID_35713 Human_SNP_ID_606562465 A-to-I Human chr16 + 67005685 67005684 67005685 CCTCACCAACATGGTGAAAACCCATCTCTACTAAAAGTACAAAAAAATTAGCCAGCTGTAGTGGC CCTCACCAACATGGTGAAAACCCATCTCTACT_AAAGTACAAAAAAATTAGCCAGCTGTAGTGGC TA T CES4A Ensembl:ENSG00000172824 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs35245817 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_107927,RMVar_hsa_circ_179017 35714 RMVar_ID_35714 Human_SNP_ID_606562999 A-to-I Human chr16 + 67007684 67007684 67007684 ACTCTGCTGCCCAGGCTAGAGTGTAGTGGTGCAATCACAGCTCACTGCAGCCTTGACCTCCCAGG ACTCTGCTGCCCAGGCTAGAGTGTAGTGGTGCCATCACAGCTCACTGCAGCCTTGACCTCCCAGG A C CES4A Ensembl:ENSG00000172824 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1441158903 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107927,RMVar_hsa_circ_179017 35715 RMVar_ID_35715 Human_SNP_ID_606569953 A-to-I Human chr16 + 67033460 67033460 67033460 CTCCTGCTTCAGCCTCCTGACTTGCTGGGATTACAGGCGCCTGCCACCACGCCTGGCTGGTTTTT CTCCTGCTTCAGCCTCCTGACTTGCTGGGATTTCAGGCGCCTGCCACCACGCCTGGCTGGTTTTT A T CBFB Ensembl:ENSG00000067955 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1329712690 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_179018,RMVar_hsa_circ_99066,RMVar_hsa_circ_118127,RMVar_hsa_circ_179019 35716 RMVar_ID_35716 Human_SNP_ID_606569965 A-to-I Human chr16 + 67033501 67033501 67033501 TGCCACCACGCCTGGCTGGTTTTTGTATTTTTAGTAGAGATGGGTTTCACCATGTTGGCCAGGCT TGCCACCACGCCTGGCTGGTTTTTGTATTTTTGGTAGAGATGGGTTTCACCATGTTGGCCAGGCT A G CBFB Ensembl:ENSG00000067955 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1472923684 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_179018,RMVar_hsa_circ_99066,RMVar_hsa_circ_118127,RMVar_hsa_circ_179019 35717 RMVar_ID_35717 Human_SNP_ID_606573801 A-to-I Human chr16 + 67047930 67047930 67047930 GTCTCTACTAGGAATGCAAAAATTGGCTGGGCATGGTGGTGGGTGCCTCTGGTCCCAGCTGCTCG GTCTCTACTAGGAATGCAAAAATTGGCTGGGCGTGGTGGTGGGTGCCTCTGGTCCCAGCTGCTCG A G CBFB Ensembl:ENSG00000067955 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1029763680 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99066,RMVar_hsa_circ_179019,RMVar_hsa_circ_179021,RMVar_hsa_circ_281379,RMVar_hsa_circ_289906,RMVar_hsa_circ_291214,RMVar_hsa_circ_179022,RMVar_hsa_circ_179020 35718 RMVar_ID_35718 Human_SNP_ID_606580278 A-to-I Human chr16 + 67072490 67072489 67072491 TTTTTCTTTTTTTTTCTTTTTTTTTTCCAGACAGAGTCTTGCTCTCTCACCCCGGCTGGAGTGCA TTTTTCTTTTTTTTTCTTTTTTTTTTCCAGAC__AGTCTTGCTCTCTCACCCCGGCTGGAGTGCA CAG C CBFB Ensembl:ENSG00000067955 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1403390278 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_2479236 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_179022,RMVar_hsa_circ_312067,RMVar_hsa_circ_303452,RMVar_hsa_circ_179023 35719 RMVar_ID_35719 Human_SNP_ID_606580584 A-to-I Human chr16 + 67073581 67073581 67073581 CAGCCTGGCCAACATGGTGAAACTCCGTCTCTACTGAAAATTCAAAAATTAGCCATGGTGGTGCG CAGCCTGGCCAACATGGTGAAACTCCGTCTCTGCTGAAAATTCAAAAATTAGCCATGGTGGTGCG A G CBFB Ensembl:ENSG00000067955 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1020717351 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12773315 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_179022,RMVar_hsa_circ_312067,RMVar_hsa_circ_303452,RMVar_hsa_circ_179023 35720 RMVar_ID_35720 Human_SNP_ID_606580621 A-to-I Human chr16 + 67073712 67073712 67073712 TGCGGTGAGCCGAGATCGTGCCATTGCACTCCAGCCTGGGCAGCAGAGTGAGACTCCATCTCAAA TGCGGTGAGCCGAGATCGTGCCATTGCACTCCGGCCTGGGCAGCAGAGTGAGACTCCATCTCAAA A G CBFB Ensembl:ENSG00000067955 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs890028096 Functional Loss SNV dbSNP153 33..33 33 - - - 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_179022,RMVar_hsa_circ_312067,RMVar_hsa_circ_303452,RMVar_hsa_circ_179023 35721 RMVar_ID_35721 Human_SNP_ID_606580678 A-to-I Human chr16 + 67073888 67073888 67073888 TGAAACCCGTCTCAACCAAAACTACAAAAATTAGCCGGGCATGGTGGAGGGCACCTGTAGTTACT TGAAACCCGTCTCAACCAAAACTACAAAAATTCGCCGGGCATGGTGGAGGGCACCTGTAGTTACT A C CBFB Ensembl:ENSG00000067955 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1407407214 Functional Loss SNV dbSNP153 33..33 33 - - - 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_179022,RMVar_hsa_circ_312067,RMVar_hsa_circ_303452,RMVar_hsa_circ_179023 35722 RMVar_ID_35722 Human_SNP_ID_606580691 A-to-I Human chr16 + 67073935 67073935 67073935 AGGGCACCTGTAGTTACTTGGGAAGCTGAGGCAGGAGAATGGCATGAACCCAGGAGGCGGAGCTT AGGGCACCTGTAGTTACTTGGGAAGCTGAGGCCGGAGAATGGCATGAACCCAGGAGGCGGAGCTT A C CBFB Ensembl:ENSG00000067955 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs551506184 Functional Loss SNV dbSNP153 33..33 33 - - - 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_179022,RMVar_hsa_circ_312067,RMVar_hsa_circ_303452,RMVar_hsa_circ_179023 35723 RMVar_ID_35723 Human_SNP_ID_606580692 A-to-I Human chr16 + 67073935 67073935 67073935 AGGGCACCTGTAGTTACTTGGGAAGCTGAGGCAGGAGAATGGCATGAACCCAGGAGGCGGAGCTT AGGGCACCTGTAGTTACTTGGGAAGCTGAGGCGGGAGAATGGCATGAACCCAGGAGGCGGAGCTT A G CBFB Ensembl:ENSG00000067955 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs551506184 Functional Loss SNV dbSNP153 33..33 33 - - - 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_179022,RMVar_hsa_circ_312067,RMVar_hsa_circ_303452,RMVar_hsa_circ_179023 35724 RMVar_ID_35724 Human_SNP_ID_606580849 A-to-I Human chr16 + 67074548 67074548 67074548 GGGACTACAGGCACGTGCCATCATACCCTGCTAATTTTTGTATTTTTAGTAGAGACGAGGTTTCA GGGACTACAGGCACGTGCCATCATACCCTGCTGATTTTTGTATTTTTAGTAGAGACGAGGTTTCA A G CBFB Ensembl:ENSG00000067955 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs943865273 Functional Loss SNV dbSNP153 33..33 33 - - - 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_179022,RMVar_hsa_circ_312067,RMVar_hsa_circ_303452,RMVar_hsa_circ_179023 35725 RMVar_ID_35725 Human_SNP_ID_606581923 A-to-I Human chr16 + 67078435 67078435 67078435 AGCTCTGGTGGCACACACCTGTAGTCCCTGCTACTTGGGAGCCTGAAGCAGGAGGATCATTTGAG AGCTCTGGTGGCACACACCTGTAGTCCCTGCTGCTTGGGAGCCTGAAGCAGGAGGATCATTTGAG A G CBFB Ensembl:ENSG00000067955 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1265808748 Functional Loss SNV dbSNP153 33..33 33 - - - 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_179022,RMVar_hsa_circ_312067,RMVar_hsa_circ_303452,RMVar_hsa_circ_179023 35726 RMVar_ID_35726 Human_SNP_ID_606581933 A-to-I Human chr16 + 67078497 67078497 67078497 GAGCTTGGGAGGTTGAGGCTGCAGTGAGCTATAATCACACCACTGCACTCCAGCCTGGGCTTGAG GAGCTTGGGAGGTTGAGGCTGCAGTGAGCTATTATCACACCACTGCACTCCAGCCTGGGCTTGAG A T CBFB Ensembl:ENSG00000067955 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs936668338 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9832090 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_179022,RMVar_hsa_circ_312067,RMVar_hsa_circ_303452,RMVar_hsa_circ_179023 35727 RMVar_ID_35727 Human_SNP_ID_606581984 A-to-I Human chr16 + 67078704 67078704 67078704 GAGTTTCGCTCTTGTTGCCCAGGCTGGAGTGCAATGGTGTGATCTTGGCTCACCGCAACCTCTGC GAGTTTCGCTCTTGTTGCCCAGGCTGGAGTGCCATGGTGTGATCTTGGCTCACCGCAACCTCTGC A C CBFB Ensembl:ENSG00000067955 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs753295959 Functional Loss SNV dbSNP153 33..33 33 - - - 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_179022,RMVar_hsa_circ_312067,RMVar_hsa_circ_303452,RMVar_hsa_circ_179023 35728 RMVar_ID_35728 Human_SNP_ID_606582015 A-to-I Human chr16 + 67078853 67078853 67078853 TTGTATTTGTTTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGGCTGGTCTCTTCAACTCC TTGTATTTGTTTTTTAGTAGAGACGGGGTTTCGCCATGTTGGCCAGGGCTGGTCTCTTCAACTCC A G CBFB Ensembl:ENSG00000067955 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs932874495 Functional Loss SNV dbSNP153 33..33 33 - - - 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_179022,RMVar_hsa_circ_312067,RMVar_hsa_circ_303452,RMVar_hsa_circ_179023 35729 RMVar_ID_35729 Human_SNP_ID_606582016 A-to-I Human chr16 + 67078856 67078856 67078856 TATTTGTTTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGGCTGGTCTCTTCAACTCCCAA TATTTGTTTTTTAGTAGAGACGGGGTTTCACCCTGTTGGCCAGGGCTGGTCTCTTCAACTCCCAA A C CBFB Ensembl:ENSG00000067955 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1014970692 Functional Loss SNV dbSNP153 33..33 33 - - - 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_179022,RMVar_hsa_circ_312067,RMVar_hsa_circ_303452,RMVar_hsa_circ_179023 35730 RMVar_ID_35730 Human_SNP_ID_606582017 A-to-I Human chr16 + 67078856 67078856 67078856 TATTTGTTTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGGCTGGTCTCTTCAACTCCCAA TATTTGTTTTTTAGTAGAGACGGGGTTTCACCGTGTTGGCCAGGGCTGGTCTCTTCAACTCCCAA A G CBFB Ensembl:ENSG00000067955 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1014970692 Functional Loss SNV dbSNP153 33..33 33 - - - 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_179022,RMVar_hsa_circ_312067,RMVar_hsa_circ_303452,RMVar_hsa_circ_179023 35731 RMVar_ID_35731 Human_SNP_ID_606582784 A-to-I Human chr16 + 67081876 67081876 67081876 TTTTCCTTTTTTTTTGAGACAGGCTGGAGTGCAATGGCGCAATCTCGGCTCACTGCAACCTTCAC TTTTCCTTTTTTTTTGAGACAGGCTGGAGTGCCATGGCGCAATCTCGGCTCACTGCAACCTTCAC A C CBFB Ensembl:ENSG00000067955 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs894414130 Functional Loss SNV dbSNP153 33..33 33 - - - 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_179022,RMVar_hsa_circ_312067,RMVar_hsa_circ_303452,RMVar_hsa_circ_179023 35732 RMVar_ID_35732 Human_SNP_ID_606583265 A-to-I Human chr16 + 67083533 67083525 67083534 GGTCAGGCTGGTCTCGGACTCCTGACCTCATGATCCACCCACCTCAACCTCCCAAAGTGCTTGGA GGTCAGGCTGGTCTCGGACTCCTGA_________CCACCCACCTCAACCTCCCAAAGTGCTTGGA ACCTCATGAT A CBFB Ensembl:ENSG00000067955 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1358945054 Functional Loss DEL dbSNP153 26..34 33 - - - Human_RBP_ID_25220175 RMVar_hsa_circ_80501,RMVar_hsa_circ_179023 35733 RMVar_ID_35733 Human_SNP_ID_606596475 A-to-I Human chr16 + 67136197 67136196 67136197 GTGGTAAAGCACGCCTGTACTCCCAGCTACTCAGGAGGCTGAGACAGGAGAATCGCTTGAACTCA GTGGTAAAGCACGCCTGTACTCCCAGCTACTC_GGAGGCTGAGACAGGAGAATCGCTTGAACTCA CA C C16orf70 Ensembl:ENSG00000125149 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1324772556 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_179025,RMVar_hsa_circ_90176,RMVar_hsa_circ_59329,RMVar_hsa_circ_56128 35734 RMVar_ID_35734 Human_SNP_ID_606596477 A-to-I Human chr16 + 67136197 67136197 67136197 GTGGTAAAGCACGCCTGTACTCCCAGCTACTCAGGAGGCTGAGACAGGAGAATCGCTTGAACTCA GTGGTAAAGCACGCCTGTACTCCCAGCTACTCGGGAGGCTGAGACAGGAGAATCGCTTGAACTCA A G C16orf70 Ensembl:ENSG00000125149 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs781638948 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_179025,RMVar_hsa_circ_90176,RMVar_hsa_circ_59329,RMVar_hsa_circ_56128 35735 RMVar_ID_35735 Human_SNP_ID_606596687 A-to-I Human chr16 + 67136809 67136809 67136809 CCCTATGTTGCCCAGGCTGGTCTCAAACTCCTAGCCTTAAGCGGTCGTCCCACCTCAGCCTCCCA CCCTATGTTGCCCAGGCTGGTCTCAAACTCCTGGCCTTAAGCGGTCGTCCCACCTCAGCCTCCCA A G C16orf70 Ensembl:ENSG00000125149 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1008977606 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_179025,RMVar_hsa_circ_90176,RMVar_hsa_circ_59329,RMVar_hsa_circ_56128 35736 RMVar_ID_35736 Human_SNP_ID_606628426 A-to-I Human chr16 + 67240340 67240340 67240340 CCTAAGGTCAGGAGTTCTAGACCAGCCTGGCCAACGTGGTGAAACCCCGTCTCTACAAAAATGCA CCTAAGGTCAGGAGTTCTAGACCAGCCTGGCCGACGTGGTGAAACCCCGTCTCTACAAAAATGCA A G SLC9A5 Ensembl:ENSG00000135740 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs778371027 Functional Loss SNV dbSNP153 33..33 33 - - - 35737 RMVar_ID_35737 Human_SNP_ID_606635077 A-to-I Human chr16 - 67268150 67268150 67268150 AAAAAAGGCTGGGCATGATGGTGTGTGCCTGTAGTCCCAGCTACTCGGGAGGCTAAGGCAAAAGG AAAAAAGGCTGGGCATGATGGTGTGTGCCTGTGGTCCCAGCTACTCGGGAGGCTAAGGCAAAAGG T C lnc-KCTD19-1-002 RNACentral:URS00008B8D7E lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264466994 Functional Loss SNV dbSNP153 33..33 33 - - - 35738 RMVar_ID_35738 Human_SNP_ID_606636583 A-to-I Human chr16 - 67273375 67273375 67273375 AAAGCAGGAGGATTATTTGAGGTCAGGAGTTCAAGAACAGCCTGAGCAACATTGTGAGGCCCTAC AAAGCAGGAGGATTATTTGAGGTCAGGAGTTCGAGAACAGCCTGAGCAACATTGTGAGGCCCTAC T C lnc-KCTD19-1-002 RNACentral:URS00008B8D7E lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1366298772 Functional Loss SNV dbSNP153 33..33 33 - - - 35739 RMVar_ID_35739 Human_SNP_ID_606677144 A-to-I Human chr16 - 67438515 67438515 67438515 ACTACATCCCTATCTTCTAGCGTCCTGGCCCAAGGCTCTCAATTGCACTCTTTGTGTGTGTGTGT ACTACATCCCTATCTTCTAGCGTCCTGGCCCAGGGCTCTCAATTGCACTCTTTGTGTGTGTGTGT T C ATP6V0D1 Ensembl:ENSG00000159720 Protein coding exon GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1010271486 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12775250,Human_RBP_ID_23695944,Human_RBP_ID_27444094 Human_miRNA_ID_2019944,Human_miRNA_ID_2025039,Human_miRNA_ID_2311655,Human_miRNA_ID_2313673,Human_miRNA_ID_2499769,Human_miRNA_ID_2607551,Human_miRNA_ID_2655460 RMVar_hsa_circ_87078,RMVar_hsa_circ_179077,RMVar_hsa_circ_78030,RMVar_hsa_circ_179076 35740 RMVar_ID_35740 Human_SNP_ID_606683002 A-to-I Human chr16 - 67464032 67464032 67464032 TCCCATGCCCCCAACCCTTTAACCTTCAAACTAGATACCATATCACAAGGCCTGGGAGAGCACAG TCCCATGCCCCCAACCCTTTAACCTTCAAACTGGATACCATATCACAAGGCCTGGGAGAGCACAG T C ATP6V0D1 Ensembl:ENSG00000159720 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1410985676 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85319,RMVar_hsa_circ_117044,RMVar_hsa_circ_179078,RMVar_hsa_circ_179082 35741 RMVar_ID_35741 Human_SNP_ID_606684735 A-to-I Human chr16 - 67471280 67471280 67471280 GGGAGGGTGAGGCAGGAGAATTGCTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCCAGGGTCACC GGGAGGGTGAGGCAGGAGAATTGCTTGAACCCGGGAGGCAGAGGTTGCAGTGAGCCAGGGTCACC T C ATP6V0D1 Ensembl:ENSG00000159720 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223308664 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85319,RMVar_hsa_circ_117044,RMVar_hsa_circ_179078,RMVar_hsa_circ_179082 35742 RMVar_ID_35742 Human_SNP_ID_606686049 A-to-I Human chr16 - 67477007 67477007 67477007 TTTTTTTTTTTTTTAATTTGAGACAGAGTCTCACTCTGTCACCCAGGCTGGACATCTCGGCTCAC TTTTTTTTTTTTTTAATTTGAGACAGAGTCTCGCTCTGTCACCCAGGCTGGACATCTCGGCTCAC T C ATP6V0D1 Ensembl:ENSG00000159720 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1248480860 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85319,RMVar_hsa_circ_117044,RMVar_hsa_circ_179078,RMVar_hsa_circ_179082 35743 RMVar_ID_35743 Human_SNP_ID_606688935 A-to-I Human chr16 + 67487763 67487763 67487763 AAAACCCTGTCTCTTCAAAAATTACAAAAATTAGCTAGACATGGTGGCGCAAGCCTGTAGTCCCA AAAACCCTGTCTCTTCAAAAATTACAAAAATTGGCTAGACATGGTGGCGCAAGCCTGTAGTCCCA A G AC009061.2 Ensembl:ENSG00000270049 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1164059834 Functional Loss SNV dbSNP153 33..33 33 - - - 35744 RMVar_ID_35744 Human_SNP_ID_606689827 A-to-I Human chr16 + 67491443 67491443 67491443 TCTCCTGCCTCAGCCTCCCGAGTAGCTGTTCTACAGGCGCCCACCACCACACCCGGCTAATTTTT TCTCCTGCCTCAGCCTCCCGAGTAGCTGTTCTTCAGGCGCCCACCACCACACCCGGCTAATTTTT A T AC009061.2 Ensembl:ENSG00000270049 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1194302634 Functional Loss SNV dbSNP153 33..33 33 - - - 35745 RMVar_ID_35745 Human_SNP_ID_606690420 A-to-I Human chr16 + 67494061 67494061 67494061 GTTGCCCAGGCCGGTCTCAAACTCCTGGACTCAAGTGATTCTCCCACCTCTGCCTCCCAAAGTGT GTTGCCCAGGCCGGTCTCAAACTCCTGGACTCGAGTGATTCTCCCACCTCTGCCTCCCAAAGTGT A G AC009061.2 Ensembl:ENSG00000270049 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1326516425 Functional Loss SNV dbSNP153 33..33 33 - - - 35746 RMVar_ID_35746 Human_SNP_ID_606693058 A-to-I Human chr16 + 67504718 67504718 67504718 TGACTCACTGCAGCCTCAACCTCCTGTGCTCAAACAATCCTCCCACCTCAGCCTCCCTAATAGCT TGACTCACTGCAGCCTCAACCTCCTGTGCTCAGACAATCCTCCCACCTCAGCCTCCCTAATAGCT A G AC009061.2 Ensembl:ENSG00000270049 lincRNA exon GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs915893317 Functional Loss SNV dbSNP153 33..33 33 - - - 35747 RMVar_ID_35747 Human_SNP_ID_606709619 A-to-I Human chr16 + 67566681 67566681 67566681 TCACTGCAAGCTCTACCTCCCAGGTTCACGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGA TCACTGCAAGCTCTACCTCCCAGGTTCACGCCGTTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGA A G CTCF Ensembl:ENSG00000102974 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1315666918 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104522,RMVar_hsa_circ_179087 35748 RMVar_ID_35748 Human_SNP_ID_606712173 A-to-I Human chr16 + 67575128 67575128 67575128 TTCTTTAGTCACGCGTTGTGTTGCATGCCTGTAGTCCTAGCTATTCAGGAGGCTGAGGCCGGAGG TTCTTTAGTCACGCGTTGTGTTGCATGCCTGTCGTCCTAGCTATTCAGGAGGCTGAGGCCGGAGG A C CTCF Ensembl:ENSG00000102974 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1324354953 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17564693 RMVar_hsa_circ_58083,RMVar_hsa_circ_346924,RMVar_hsa_circ_104522,RMVar_hsa_circ_377450,RMVar_hsa_circ_179087,RMVar_hsa_circ_91373,RMVar_hsa_circ_345675,RMVar_hsa_circ_75098,RMVar_hsa_circ_179089,RMVar_hsa_circ_179090,RMVar_hsa_circ_179088 35749 RMVar_ID_35749 Human_SNP_ID_606714785 A-to-I Human chr16 + 67583564 67583564 67583564 CAAAACTTAGCCGGGTGTAGTGGGGCATGCCTATAATCTCAGCCACTCGGGAGGCCGAGGCAGGA CAAAACTTAGCCGGGTGTAGTGGGGCATGCCTGTAATCTCAGCCACTCGGGAGGCCGAGGCAGGA A G CTCF Ensembl:ENSG00000102974 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs759147574 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6526866 RMVar_hsa_circ_58083,RMVar_hsa_circ_346924,RMVar_hsa_circ_104522,RMVar_hsa_circ_377450,RMVar_hsa_circ_179087,RMVar_hsa_circ_91373,RMVar_hsa_circ_345675,RMVar_hsa_circ_75098,RMVar_hsa_circ_179089,RMVar_hsa_circ_179090,RMVar_hsa_circ_179088 35750 RMVar_ID_35750 Human_SNP_ID_606717581 A-to-I Human chr16 + 67592933 67592933 67592933 CCTGTAGTCCCAGCTACTTAGGAGGCTGAGGCAGGAGAATCGGTTGAACCTGGAGGCAGGGGTTG CCTGTAGTCCCAGCTACTTAGGAGGCTGAGGCGGGAGAATCGGTTGAACCTGGAGGCAGGGGTTG A G CTCF Ensembl:ENSG00000102974 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs568350725 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58083,RMVar_hsa_circ_346924,RMVar_hsa_circ_104522,RMVar_hsa_circ_377450,RMVar_hsa_circ_179087,RMVar_hsa_circ_91373,RMVar_hsa_circ_345675,RMVar_hsa_circ_75098,RMVar_hsa_circ_179089,RMVar_hsa_circ_179090,RMVar_hsa_circ_179088 35751 RMVar_ID_35751 Human_SNP_ID_606720009 A-to-I Human chr16 + 67601549 67601549 67601549 TATTTCTAGTCGAGATGGGGTTTCACCATGTTAGCCAGGATGGTCTCGATCTCCTGACCTCGGGG TATTTCTAGTCGAGATGGGGTTTCACCATGTTGGCCAGGATGGTCTCGATCTCCTGACCTCGGGG A G CTCF Ensembl:ENSG00000102974 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1309124952 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58083,RMVar_hsa_circ_346924,RMVar_hsa_circ_104522,RMVar_hsa_circ_377450,RMVar_hsa_circ_179087,RMVar_hsa_circ_91373,RMVar_hsa_circ_345675,RMVar_hsa_circ_75098,RMVar_hsa_circ_179089,RMVar_hsa_circ_179090,RMVar_hsa_circ_179088 35752 RMVar_ID_35752 Human_SNP_ID_606726446 A-to-I Human chr16 + 67623407 67623407 67623407 TCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGTGGATCATTTGAGCTTAGGAGTTCC TCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGTGGATCATTTGAGCTTAGGAGTTCC A G CTCF Ensembl:ENSG00000102974 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1333701064 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1728208,Human_Splice_Rec_1728209 RMVar_hsa_circ_7522,RMVar_hsa_circ_104522,RMVar_hsa_circ_179087,RMVar_hsa_circ_91373,RMVar_hsa_circ_345675,RMVar_hsa_circ_179089,RMVar_hsa_circ_357839,RMVar_hsa_circ_179088,RMVar_hsa_circ_347814,RMVar_hsa_circ_310170,RMVar_hsa_circ_24105,RMVar_hsa_circ_179096,RMVar_hsa_circ_36848,RMVar_hsa_circ_24370,RMVar_hsa_circ_311413,RMVar_hsa_circ_179097,RMVar_hsa_circ_337919,RMVar_hsa_circ_268048,RMVar_hsa_circ_179099,RMVar_hsa_circ_322461,RMVar_hsa_circ_179098,RMVar_hsa_circ_179103,RMVar_hsa_circ_179104,RMVar_hsa_circ_85455 35753 RMVar_ID_35753 Human_SNP_ID_606727074 A-to-I Human chr16 + 67625064 67625064 67625064 CTCCTTCCTCATTTTCCCGAGTAGCTGGGACCACAGGTGTACGCCACCATGCCTAGCTAATTTTT CTCCTTCCTCATTTTCCCGAGTAGCTGGGACCTCAGGTGTACGCCACCATGCCTAGCTAATTTTT A T CTCF Ensembl:ENSG00000102974 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1050867143 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7522,RMVar_hsa_circ_104522,RMVar_hsa_circ_179087,RMVar_hsa_circ_91373,RMVar_hsa_circ_345675,RMVar_hsa_circ_179089,RMVar_hsa_circ_357839,RMVar_hsa_circ_179088,RMVar_hsa_circ_347814,RMVar_hsa_circ_310170,RMVar_hsa_circ_24105,RMVar_hsa_circ_179096,RMVar_hsa_circ_36848,RMVar_hsa_circ_24370,RMVar_hsa_circ_311413,RMVar_hsa_circ_179097,RMVar_hsa_circ_337919,RMVar_hsa_circ_268048,RMVar_hsa_circ_179099,RMVar_hsa_circ_322461,RMVar_hsa_circ_179098,RMVar_hsa_circ_179103,RMVar_hsa_circ_179104,RMVar_hsa_circ_85455 35754 RMVar_ID_35754 Human_SNP_ID_606727091 A-to-I Human chr16 + 67625109 67625108 67625110 ACCATGCCTAGCTAATTTTTGTATTTTTCAGTAGAGACGGGTTTCACTATATGTTGGCCAGGCCA ACCATGCCTAGCTAATTTTTGTATTTTTCAGT__AGACGGGTTTCACTATATGTTGGCCAGGCCA TAG T CTCF Ensembl:ENSG00000102974 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs995460652 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_12777224 RMVar_hsa_circ_7522,RMVar_hsa_circ_104522,RMVar_hsa_circ_179087,RMVar_hsa_circ_91373,RMVar_hsa_circ_345675,RMVar_hsa_circ_179089,RMVar_hsa_circ_357839,RMVar_hsa_circ_179088,RMVar_hsa_circ_347814,RMVar_hsa_circ_310170,RMVar_hsa_circ_24105,RMVar_hsa_circ_179096,RMVar_hsa_circ_36848,RMVar_hsa_circ_24370,RMVar_hsa_circ_311413,RMVar_hsa_circ_179097,RMVar_hsa_circ_337919,RMVar_hsa_circ_268048,RMVar_hsa_circ_179099,RMVar_hsa_circ_322461,RMVar_hsa_circ_179098,RMVar_hsa_circ_179103,RMVar_hsa_circ_179104,RMVar_hsa_circ_85455 35755 RMVar_ID_35755 Human_SNP_ID_606730351 A-to-I Human chr16 + 67635672 67635671 67635673 CCACCACGCCCAGCTAATTTTATATTTTTAGTAGAGTCAGGGTTTCTCCATGTTGGACAGGCTGG CCACCACGCCCAGCTAATTTTATATTTTTAGT__AGTCAGGGTTTCTCCATGTTGGACAGGCTGG TAG T CTCF Ensembl:ENSG00000102974 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1455029529 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_310170,RMVar_hsa_circ_268048 35756 RMVar_ID_35756 Human_SNP_ID_606730352 A-to-I Human chr16 + 67635672 67635672 67635672 CCACCACGCCCAGCTAATTTTATATTTTTAGTAGAGTCAGGGTTTCTCCATGTTGGACAGGCTGG CCACCACGCCCAGCTAATTTTATATTTTTAGTGGAGTCAGGGTTTCTCCATGTTGGACAGGCTGG A G CTCF Ensembl:ENSG00000102974 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs541556839 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_310170,RMVar_hsa_circ_268048 35757 RMVar_ID_35757 Human_SNP_ID_606730366 A-to-I Human chr16 + 67635763 67635721 67635763 CACCCACCTCAGCCTCCCAAAGTACTGGGATTACAGGTGTGAGCCACCACGCCCAGCTGCCAGTT _________________________________CAGGTGTGAGCCACCACGCCCAGCTGCCAGTT TCAGGTGATACACCCACCTCAGCCTCCCAAAGTACTGGGATTA T CTCF Ensembl:ENSG00000102974 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1405188293 Functional Loss DEL dbSNP153 1..33 33 - - - RMVar_hsa_circ_310170,RMVar_hsa_circ_268048 35758 RMVar_ID_35758 Human_SNP_ID_606730385 A-to-I Human chr16 + 67635815 67635815 67635815 CCAGCTGCCAGTTTCTTATTTCTTGTAGAGATAAGGTCTCACTATGTTACCCAAGCTGGTCTTGA CCAGCTGCCAGTTTCTTATTTCTTGTAGAGATGAGGTCTCACTATGTTACCCAAGCTGGTCTTGA A G CTCF Ensembl:ENSG00000102974 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs941595368 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_310170,RMVar_hsa_circ_268048 35759 RMVar_ID_35759 Human_SNP_ID_606744579 A-to-I Human chr16 - 67678314 67678314 67678314 GTGCCACCACGCCCAGCGAATTTTGTATTTTTAGTAGAGACGGGGTTTCTTCCTGCTAGTTAGGC GTGCCACCACGCCCAGCGAATTTTGTATTTTTGGTAGAGACGGGGTTTCTTCCTGCTAGTTAGGC T C GFOD2 Ensembl:ENSG00000141098 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs573686090 Functional Loss SNV dbSNP153 33..33 33 - - - 35760 RMVar_ID_35760 Human_SNP_ID_606744771 A-to-I Human chr16 - 67679045 67679045 67679045 GTCCTACCTCAGTCTCCCAAGTAGCTGGGGCTACAGGTACACGCCACCACGCCTGGCTTATTTTT GTCCTACCTCAGTCTCCCAAGTAGCTGGGGCTGCAGGTACACGCCACCACGCCTGGCTTATTTTT T C GFOD2 Ensembl:ENSG00000141098 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1054021155 Functional Loss SNV dbSNP153 33..33 33 - - - 35761 RMVar_ID_35761 Human_SNP_ID_606744870 A-to-I Human chr16 - 67679357 67679357 67679357 TGGTGGCAGGCTCCTGTAATCCCAGCTAGCTCAGGAGGCTGAGGCAGGAAAGTCACTTGAACCCA TGGTGGCAGGCTCCTGTAATCCCAGCTAGCTCTGGAGGCTGAGGCAGGAAAGTCACTTGAACCCA T A GFOD2 Ensembl:ENSG00000141098 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1415403889 Functional Loss SNV dbSNP153 33..33 33 - - - 35762 RMVar_ID_35762 Human_SNP_ID_606745427 A-to-I Human chr16 - 67681682 67681682 67681682 ATTCAGGGTTGGGCTCAGTGCCTCACACCTCTAATCCAGCACTTTGGGAGGCCAAGGTGGGCAGA ATTCAGGGTTGGGCTCAGTGCCTCACACCTCTTATCCAGCACTTTGGGAGGCCAAGGTGGGCAGA T A GFOD2 Ensembl:ENSG00000141098 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893844404 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269522 35763 RMVar_ID_35763 Human_SNP_ID_606745491 A-to-I Human chr16 - 67681987 67681987 67681987 TTTGTAGAGACAGGATCTTGCTGTGTTGTTCAAGCTGGTTTCGAACTCCTAACCTCAGGCAATCA TTTGTAGAGACAGGATCTTGCTGTGTTGTTCAGGCTGGTTTCGAACTCCTAACCTCAGGCAATCA T C GFOD2 Ensembl:ENSG00000141098 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,31158229,31158229,32596459 RNA-Seq:(High) rs544866621 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269522 35764 RMVar_ID_35764 Human_SNP_ID_606745536 A-to-I Human chr16 - 67682178 67682178 67682178 CAAAAATTAGCTGGGCGTGTTGGCACGTGCCTATAGTCCCAGCTACTCAGGAGGCTGAGGCAGGA CAAAAATTAGCTGGGCGTGTTGGCACGTGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGA T C GFOD2 Ensembl:ENSG00000141098 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1055301208 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269522 35765 RMVar_ID_35765 Human_SNP_ID_606745550 A-to-I Human chr16 - 67682220 67682220 67682220 CAGCCTGACCAACCTGGTGAAACCTCGTCTATACTAAAAACACAAAAATTAGCTGGGCGTGTTGG CAGCCTGACCAACCTGGTGAAACCTCGTCTATGCTAAAAACACAAAAATTAGCTGGGCGTGTTGG T C GFOD2 Ensembl:ENSG00000141098 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1160052340 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269522 35766 RMVar_ID_35766 Human_SNP_ID_606745976 A-to-I Human chr16 - 67684257 67684257 67684257 GCGATACTCCTGCCTCGGCTTTGCAAGTAGCCAGGACTACAGGCATGTGCCACCACGCCCAGCTA GCGATACTCCTGCCTCGGCTTTGCAAGTAGCCGGGACTACAGGCATGTGCCACCACGCCCAGCTA T C GFOD2 Ensembl:ENSG00000141098 Protein coding intron GSE38233;GSE107867 cultured B-cells;ASD brains,frontal_cortex - 24183664,30559470 RNA-Seq:(High) rs1413546876 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22203946 RMVar_hsa_circ_179113,RMVar_hsa_circ_269522 35767 RMVar_ID_35767 Human_SNP_ID_606745987 A-to-I Human chr16 - 67684321 67684321 67684321 GCCCAGGCTGGAGTGTGCATTGGTGCAATCTCAGCTCACTGCAACCTCCACCTCCCAGGTTCAAG GCCCAGGCTGGAGTGTGCATTGGTGCAATCTCGGCTCACTGCAACCTCCACCTCCCAGGTTCAAG T C GFOD2 Ensembl:ENSG00000141098 Protein coding intron GSE38233;GSE107867 cultured B-cells;ASD brains,temporal_cortex - 24183664,30559470 RNA-Seq:(High) rs1555545224 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_179113,RMVar_hsa_circ_269522 35768 RMVar_ID_35768 Human_SNP_ID_606750525 A-to-I Human chr16 - 67702302 67702302 67702302 GCCTGGCTAATTTGTGTATTTTTAGCAGAGACAGTGTTTCACATGTTGGTCTCAAACTCCTAGCC GCCTGGCTAATTTGTGTATTTTTAGCAGAGACGGTGTTTCACATGTTGGTCTCAAACTCCTAGCC T C GFOD2 Ensembl:ENSG00000141098 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs555724486 Functional Loss SNV dbSNP153 33..33 33 - - - 35769 RMVar_ID_35769 Human_SNP_ID_606751412 A-to-I Human chr16 - 67705940 67705940 67705940 GGGAAAACCATAACAGGCACTTTTTTTTTTTTAAAGATAGAGTTTCACTCTGTTGCCCAGCCTGG GGGAAAACCATAACAGGCACTTTTTTTTTTTTTAAGATAGAGTTTCACTCTGTTGCCCAGCCTGG T A GFOD2 Ensembl:ENSG00000141098 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1386234392 Functional Loss SNV dbSNP153 33..33 33 - - - 35770 RMVar_ID_35770 Human_SNP_ID_606752393 A-to-I Human chr16 - 67710194 67710194 67710194 TTGAGCCCAGGAGTTCGAGGCTACAGTAAGCTATGATCGCCCCACTGCACTCCGGCCTGACCAAC TTGAGCCCAGGAGTTCGAGGCTACAGTAAGCTGTGATCGCCCCACTGCACTCCGGCCTGACCAAC T C GFOD2 Ensembl:ENSG00000141098 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs544885017 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12777573,Human_RBP_ID_25220873 35771 RMVar_ID_35771 Human_SNP_ID_606765742 A-to-I Human chr16 - 67766017 67766017 67766017 ATTTTGAGACTTTGGTGTTTGTTTATTTATTTATTTATCTGAGACAGGGTCTTACTCTGTCTCCC ATTTTGAGACTTTGGTGTTTGTTTATTTATTTGTTTATCTGAGACAGGGTCTTACTCTGTCTCCC T C RANBP10 Ensembl:ENSG00000141084 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1292719919 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3497610 RMVar_hsa_circ_336505,RMVar_hsa_circ_112950,RMVar_hsa_circ_179122,RMVar_hsa_circ_179121,RMVar_hsa_circ_34349,RMVar_hsa_circ_298267,RMVar_hsa_circ_179123 35772 RMVar_ID_35772 Human_SNP_ID_606766500 A-to-I Human chr16 - 67769240 67769240 67769240 ACAGGGTTTCACCAGGTTGCCCAGACTCGTCTAGAACTCCTGAGCTCAAGCAGTCCACCCATCTC ACAGGGTTTCACCAGGTTGCCCAGACTCGTCTGGAACTCCTGAGCTCAAGCAGTCCACCCATCTC T C RANBP10 Ensembl:ENSG00000141084 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1392534902 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12778152 RMVar_hsa_circ_336505,RMVar_hsa_circ_112950,RMVar_hsa_circ_179122,RMVar_hsa_circ_179121,RMVar_hsa_circ_34349,RMVar_hsa_circ_298267,RMVar_hsa_circ_179123 35773 RMVar_ID_35773 Human_SNP_ID_606767434 A-to-I Human chr16 - 67772788 67772788 67772788 TGGGTGCCATTCTACCTCCAGGTGTCAATGACACAGGGAGCAGCCCCACAGGAGCCCAGGTTGCA TGGGTGCCATTCTACCTCCAGGTGTCAATGACCCAGGGAGCAGCCCCACAGGAGCCCAGGTTGCA T G RANBP10 Ensembl:ENSG00000141084 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1010494192 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112950,RMVar_hsa_circ_179121 35774 RMVar_ID_35774 Human_SNP_ID_606767436 A-to-I Human chr16 - 67772793 67772793 67772793 ACATTTGGGTGCCATTCTACCTCCAGGTGTCAATGACACAGGGAGCAGCCCCACAGGAGCCCAGG ACATTTGGGTGCCATTCTACCTCCAGGTGTCAGTGACACAGGGAGCAGCCCCACAGGAGCCCAGG T C RANBP10 Ensembl:ENSG00000141084 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs118016432 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112950,RMVar_hsa_circ_179121 35775 RMVar_ID_35775 Human_SNP_ID_606767437 A-to-I Human chr16 - 67772801 67772801 67772801 TGACACCCACATTTGGGTGCCATTCTACCTCCAGGTGTCAATGACACAGGGAGCAGCCCCACAGG TGACACCCACATTTGGGTGCCATTCTACCTCCGGGTGTCAATGACACAGGGAGCAGCCCCACAGG T C RANBP10 Ensembl:ENSG00000141084 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1446076202 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112950,RMVar_hsa_circ_179121 35776 RMVar_ID_35776 Human_SNP_ID_606769913 A-to-I Human chr16 - 67782806 67782806 67782806 CTTTTAAGAGATGGCTCTTAAAAGTGGCTTTTAAGAGATGGCTCTTAAAAGTGGCTTTTAAGAGA CTTTTAAGAGATGGCTCTTAAAAGTGGCTTTTGAGAGATGGCTCTTAAAAGTGGCTTTTAAGAGA T C RANBP10 Ensembl:ENSG00000141084 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1325071592 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112950,RMVar_hsa_circ_179121 35777 RMVar_ID_35777 Human_SNP_ID_606785408 A-to-I Human chr16 - 67838442 67838442 67838442 AATTTTTGTGTTTTTAGTAAAGATGAGGTTTCACCACGTTGTCCGGGCTGGTCTCGAACTCCTGA AATTTTTGTGTTTTTAGTAAAGATGAGGTTTCGCCACGTTGTCCGGGCTGGTCTCGAACTCCTGA T C CENPT Ensembl:ENSG00000102901 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs544442562 Functional Loss SNV dbSNP153 33..33 33 - - - 35778 RMVar_ID_35778 Human_SNP_ID_606785518 A-to-I Human chr16 - 67838850 67838850 67838850 CAATCTCAGTTCACTGTAATCTCTGCCTCCCGAGTTCACACGATTTTCCTGCCTCAGCCTCCTGA CAATCTCAGTTCACTGTAATCTCTGCCTCCCGGGTTCACACGATTTTCCTGCCTCAGCCTCCTGA T C CENPT Ensembl:ENSG00000102901 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1000657579 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12778876 35779 RMVar_ID_35779 Human_SNP_ID_606785583 A-to-I Human chr16 - 67839054 67839054 67839054 AAGAGATGGAGTTTCAACATGTTGGGCAGGCTAGTCTGGAACTTCTGACCTCAGGTGATCCGGCC AAGAGATGGAGTTTCAACATGTTGGGCAGGCTGGTCTGGAACTTCTGACCTCAGGTGATCCGGCC T C CENPT Ensembl:ENSG00000102901 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1015152032 Functional Loss SNV dbSNP153 33..33 33 - - - 35780 RMVar_ID_35780 Human_SNP_ID_606788738 A-to-I Human chr16 + 67848528 67848528 67848528 TTGCTTGAACCCGGGAGGTGGAGGTCGCAGTGAACTGAGATCATGCCACTGTACTCCAGCCTGGG TTGCTTGAACCCGGGAGGTGGAGGTCGCAGTGGACTGAGATCATGCCACTGTACTCCAGCCTGGG A G NUTF2 Ensembl:ENSG00000102898 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs934731892 Functional Loss SNV dbSNP153 33..33 33 - - - 35781 RMVar_ID_35781 Human_SNP_ID_606789151 A-to-I Human chr16 + 67850044 67850044 67850044 AAACTCCTGAGTTCAAGCGATACTCCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGATGTGAA AAACTCCTGAGTTCAAGCGATACTCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGATGTGAA A G NUTF2 Ensembl:ENSG00000102898 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1343186943 Functional Loss SNV dbSNP153 33..33 33 - - - 35782 RMVar_ID_35782 Human_SNP_ID_606789522 A-to-I Human chr16 + 67851299 67851299 67851299 GGTTAGGAGTTGGAGACCAGCTTGGCCAATATAGTGAAACTCTGTTTCTATTAAAAATACAAAAA GGTTAGGAGTTGGAGACCAGCTTGGCCAATATGGTGAAACTCTGTTTCTATTAAAAATACAAAAA A G NUTF2 Ensembl:ENSG00000102898 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1196587150 Functional Loss SNV dbSNP153 33..33 33 - - - 35783 RMVar_ID_35783 Human_SNP_ID_606790242 A-to-I Human chr16 + 67853999 67853999 67853999 TTGAGATGGAGTTTCGCTCTGTCACCTAGGCTAGAGTGCAGTAGCATGATCTCAGCTCACTACAG TTGAGATGGAGTTTCGCTCTGTCACCTAGGCTGGAGTGCAGTAGCATGATCTCAGCTCACTACAG A G NUTF2 Ensembl:ENSG00000102898 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1203725779 Functional Loss SNV dbSNP153 33..33 33 - - - 35784 RMVar_ID_35784 Human_SNP_ID_606790296 A-to-I Human chr16 + 67854211 67854211 67854211 GAACTCTTGGTCTGCCCGCCTTGGCCTCCCAAAATGCTGGGATTACAGGCGTGAGCCACTGCTTG GAACTCTTGGTCTGCCCGCCTTGGCCTCCCAAGATGCTGGGATTACAGGCGTGAGCCACTGCTTG A G NUTF2 Ensembl:ENSG00000102898 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1337021190 Functional Loss SNV dbSNP153 33..33 33 - - - 35785 RMVar_ID_35785 Human_SNP_ID_606798376 A-to-I Human chr16 + 67884336 67884336 67884336 GCGTGTGGTAGTCAGAAGGTTTAGCTGGGCCCAGGGCAGGTATTGCGCCTGCTTGGGTTCTGCCA GCGTGTGGTAGTCAGAAGGTTTAGCTGGGCCCGGGGCAGGTATTGCGCCTGCTTGGGTTCTGCCA A G AC040162.3,EDC4 Ensembl:ENSG00000263126,Ensembl:ENSG00000038358 lincRNA,Protein coding exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs11558520 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1005098,Human_RBP_ID_5141935,Human_RBP_ID_5575965,Human_RBP_ID_6527532,Human_RBP_ID_8188891,Human_RBP_ID_8436875,Human_RBP_ID_8809237,Human_RBP_ID_23209395,Human_RBP_ID_23696317 Human_miRNA_ID_3214575 35786 RMVar_ID_35786 Human_SNP_ID_606802164 A-to-I Human chr16 + 67898238 67898238 67898238 TTGGGCTCAAGAGTTCGAGAACAAGCCTGGGCAACATGGTGAAACCCTGTCTCTACTGAAAATAC TTGGGCTCAAGAGTTCGAGAACAAGCCTGGGCCACATGGTGAAACCCTGTCTCTACTGAAAATAC A C PSKH1 Ensembl:ENSG00000159792 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1480690552 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17564223 35787 RMVar_ID_35787 Human_SNP_ID_606803187 A-to-I Human chr16 + 67902424 67902424 67902424 TCAAGCGATTCTCCTACCTCAGCCTCCTGAGCAGCTGGGATTACAGGCGCGTGCCATCACGTCCG TCAAGCGATTCTCCTACCTCAGCCTCCTGAGCTGCTGGGATTACAGGCGCGTGCCATCACGTCCG A T PSKH1 Ensembl:ENSG00000159792 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1351818399 Functional Loss SNV dbSNP153 33..33 33 - - - 35788 RMVar_ID_35788 Human_SNP_ID_606806120 A-to-I Human chr16 + 67913729 67913729 67913729 AGGCTGGTACTTCTCAGACTCCTGATGTTCATACACATCCCCTGGAATCTCGTTAAAATGTAGAT AGGCTGGTACTTCTCAGACTCCTGATGTTCATGCACATCCCCTGGAATCTCGTTAAAATGTAGAT A G PSKH1 Ensembl:ENSG00000159792 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1015929922 Functional Loss SNV dbSNP153 33..33 33 - - - 35789 RMVar_ID_35789 Human_SNP_ID_606837645 A-to-I Human chr16 + 68024885 68024885 68024885 AGACAGTCTCACTGTGTTGCCCAGGCTGGAGTACAGTGGTGCGATGTCAGCTCACTGCAGTCTCT AGACAGTCTCACTGTGTTGCCCAGGCTGGAGTGCAGTGGTGCGATGTCAGCTCACTGCAGTCTCT A G DUS2 Ensembl:ENSG00000167264 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs932184213 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99498,RMVar_hsa_circ_179175,RMVar_hsa_circ_87968,RMVar_hsa_circ_179174 35790 RMVar_ID_35790 Human_SNP_ID_606838456 A-to-I Human chr16 + 68028358 68028358 68028358 ATATAACAACATAATAATAGACGTTAGAGGCCAGGCGCGGTGGCTCACACCTGTAATCCCAGCAC ATATAACAACATAATAATAGACGTTAGAGGCCGGGCGCGGTGGCTCACACCTGTAATCCCAGCAC A G DUS2 Ensembl:ENSG00000167264 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs925747773 Functional Loss SNV dbSNP153 33..33 33 - - - 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_279630,RMVar_hsa_circ_280695,RMVar_hsa_circ_271056,RMVar_hsa_circ_179177,RMVar_hsa_circ_179178,RMVar_hsa_circ_179176 35791 RMVar_ID_35791 Human_SNP_ID_606838702 A-to-I Human chr16 + 68029378 68029378 68029378 TTGCCCTGACTGGTCTTGAACTCTTGGGCTCAAATGATCCTCTTGCCTCAACCTCCCAGTGTTAG TTGCCCTGACTGGTCTTGAACTCTTGGGCTCACATGATCCTCTTGCCTCAACCTCCCAGTGTTAG A C DUS2 Ensembl:ENSG00000167264 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1205794193 Functional Loss SNV dbSNP153 33..33 33 - - - 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_279630,RMVar_hsa_circ_280695,RMVar_hsa_circ_271056,RMVar_hsa_circ_179177,RMVar_hsa_circ_179178,RMVar_hsa_circ_179176 35792 RMVar_ID_35792 Human_SNP_ID_606839268 A-to-I Human chr16 + 68031768 68031768 68031768 CCAGGCTGGAGGGCAGTGGTGCGATCTTGGCTAACTGCAACCTCTGCCTCCCTGGTTTGAGTGAT CCAGGCTGGAGGGCAGTGGTGCGATCTTGGCTGACTGCAACCTCTGCCTCCCTGGTTTGAGTGAT A G DUS2 Ensembl:ENSG00000167264 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1033229010 Functional Loss SNV dbSNP153 33..33 33 - - - 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_279630,RMVar_hsa_circ_280695,RMVar_hsa_circ_271056,RMVar_hsa_circ_179177,RMVar_hsa_circ_179178,RMVar_hsa_circ_179176 35793 RMVar_ID_35793 Human_SNP_ID_606850333 A-to-I Human chr16 + 68077001 68077001 68077001 GGTCTCAGCCGGGCACGGTGGCTCATGCCTGTAATCCCACAACTTTGGGAGGCCGAGGCAGGTGG GGTCTCAGCCGGGCACGGTGGCTCATGCCTGTGATCCCACAACTTTGGGAGGCCGAGGCAGGTGG A G DUS2 Ensembl:ENSG00000167264 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs895135012 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_332664,RMVar_hsa_circ_125327,RMVar_hsa_circ_179184,RMVar_hsa_circ_14071,RMVar_hsa_circ_12132,RMVar_hsa_circ_179195 35794 RMVar_ID_35794 Human_SNP_ID_606850369 A-to-I Human chr16 + 68077193 68077193 68077193 GAGAACTGCTTAAACCTGGAGGCAGAGGTTGCAGTTAGCTGAGATCATGCCACTGCACTCCAGCC GAGAACTGCTTAAACCTGGAGGCAGAGGTTGCGGTTAGCTGAGATCATGCCACTGCACTCCAGCC A G DUS2 Ensembl:ENSG00000167264 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs756700754 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_332664,RMVar_hsa_circ_125327,RMVar_hsa_circ_179184,RMVar_hsa_circ_14071,RMVar_hsa_circ_12132,RMVar_hsa_circ_179195 35795 RMVar_ID_35795 Human_SNP_ID_606850456 A-to-I Human chr16 + 68077589 68077589 68077589 TTTTGTATTTTCAGTAGGGATGGGGTTTCACCATCTTCACCAGGCTGGTCTCGAACTCCTGACCT TTTTGTATTTTCAGTAGGGATGGGGTTTCACCGTCTTCACCAGGCTGGTCTCGAACTCCTGACCT A G AC130462.3,DUS2 Ensembl:ENSG00000261864,Ensembl:ENSG00000167264 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1181193842 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_332664,RMVar_hsa_circ_125327,RMVar_hsa_circ_179184,RMVar_hsa_circ_14071,RMVar_hsa_circ_12132,RMVar_hsa_circ_179195 35796 RMVar_ID_35796 Human_SNP_ID_606850459 A-to-I Human chr16 + 68077598 68077598 68077598 TTCAGTAGGGATGGGGTTTCACCATCTTCACCAGGCTGGTCTCGAACTCCTGACCTCAGATGATC TTCAGTAGGGATGGGGTTTCACCATCTTCACCCGGCTGGTCTCGAACTCCTGACCTCAGATGATC A C AC130462.3,DUS2 Ensembl:ENSG00000261864,Ensembl:ENSG00000167264 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs192547494 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_332664,RMVar_hsa_circ_125327,RMVar_hsa_circ_179184,RMVar_hsa_circ_14071,RMVar_hsa_circ_12132,RMVar_hsa_circ_179195 35797 RMVar_ID_35797 Human_SNP_ID_606866568 A-to-I Human chr16 + 68142647 68142647 68142647 GGGCGTGGTGGTGGGTGCCTGTAATCTCAGCTACTTGGGAGGCTGAGGCATGAGACTCATTTGAA GGGCGTGGTGGTGGGTGCCTGTAATCTCAGCTGCTTGGGAGGCTGAGGCATGAGACTCATTTGAA A G NFATC3 Ensembl:ENSG00000072736 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs189183451 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_179205,RMVar_hsa_circ_286210,RMVar_hsa_circ_179198,RMVar_hsa_circ_294649,RMVar_hsa_circ_296020,RMVar_hsa_circ_343271,RMVar_hsa_circ_291835,RMVar_hsa_circ_281495,RMVar_hsa_circ_179201,RMVar_hsa_circ_179203,RMVar_hsa_circ_179204,RMVar_hsa_circ_179202,RMVar_hsa_circ_356013,RMVar_hsa_circ_361959,RMVar_hsa_circ_179206,RMVar_hsa_circ_361224,RMVar_hsa_circ_327647,RMVar_hsa_circ_179208 35798 RMVar_ID_35798 Human_SNP_ID_606867088 A-to-I Human chr16 + 68144838 68144838 68144838 TGCCACCACGCCCAGCTGATTTTTACATTTTTAGTAGAAACAGAGTTTCAACATGTTGGCCAGGC TGCCACCACGCCCAGCTGATTTTTACATTTTTGGTAGAAACAGAGTTTCAACATGTTGGCCAGGC A G NFATC3 Ensembl:ENSG00000072736 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1351964150 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12781520 RMVar_hsa_circ_179205,RMVar_hsa_circ_286210,RMVar_hsa_circ_179198,RMVar_hsa_circ_294649,RMVar_hsa_circ_296020,RMVar_hsa_circ_343271,RMVar_hsa_circ_291835,RMVar_hsa_circ_281495,RMVar_hsa_circ_179201,RMVar_hsa_circ_179203,RMVar_hsa_circ_179204,RMVar_hsa_circ_179202,RMVar_hsa_circ_356013,RMVar_hsa_circ_361959,RMVar_hsa_circ_179206,RMVar_hsa_circ_361224,RMVar_hsa_circ_327647,RMVar_hsa_circ_179208 35799 RMVar_ID_35799 Human_SNP_ID_606867149 A-to-I Human chr16 + 68145036 68145036 68145036 CACTATGTTGCCCAGGCTGGTCTACAACTCCTAGCCTCAAGTGATCCTCCCACCTTGGCCTCCCT CACTATGTTGCCCAGGCTGGTCTACAACTCCTGGCCTCAAGTGATCCTCCCACCTTGGCCTCCCT A G NFATC3 Ensembl:ENSG00000072736 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1407070756 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_179205,RMVar_hsa_circ_286210,RMVar_hsa_circ_179198,RMVar_hsa_circ_294649,RMVar_hsa_circ_296020,RMVar_hsa_circ_343271,RMVar_hsa_circ_291835,RMVar_hsa_circ_281495,RMVar_hsa_circ_179201,RMVar_hsa_circ_179203,RMVar_hsa_circ_179204,RMVar_hsa_circ_179202,RMVar_hsa_circ_356013,RMVar_hsa_circ_361959,RMVar_hsa_circ_179206,RMVar_hsa_circ_361224,RMVar_hsa_circ_327647,RMVar_hsa_circ_179208 35800 RMVar_ID_35800 Human_SNP_ID_606867247 A-to-I Human chr16 + 68145343 68145343 68145343 TTTTATGTTTTTTGTAGAGATGGGGTTTCACCATCTTGTCCAGGCAGGCTGGTTTTGAACTCCTG TTTTATGTTTTTTGTAGAGATGGGGTTTCACCGTCTTGTCCAGGCAGGCTGGTTTTGAACTCCTG A G NFATC3 Ensembl:ENSG00000072736 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1020820095 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_179205,RMVar_hsa_circ_286210,RMVar_hsa_circ_179198,RMVar_hsa_circ_294649,RMVar_hsa_circ_296020,RMVar_hsa_circ_343271,RMVar_hsa_circ_291835,RMVar_hsa_circ_281495,RMVar_hsa_circ_179201,RMVar_hsa_circ_179203,RMVar_hsa_circ_179204,RMVar_hsa_circ_179202,RMVar_hsa_circ_356013,RMVar_hsa_circ_361959,RMVar_hsa_circ_179206,RMVar_hsa_circ_361224,RMVar_hsa_circ_327647,RMVar_hsa_circ_179208 35801 RMVar_ID_35801 Human_SNP_ID_606868908 A-to-I Human chr16 + 68152655 68152655 68152655 CTCCTGCCTCAGTCTTTCAGGTAGCTGGGACTACAGGTGCATGCCTTCACGTCTGGCTCTACCTG CTCCTGCCTCAGTCTTTCAGGTAGCTGGGACTGCAGGTGCATGCCTTCACGTCTGGCTCTACCTG A G NFATC3 Ensembl:ENSG00000072736 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1418601847 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_179205,RMVar_hsa_circ_286210,RMVar_hsa_circ_179198,RMVar_hsa_circ_294649,RMVar_hsa_circ_296020,RMVar_hsa_circ_343271,RMVar_hsa_circ_291835,RMVar_hsa_circ_281495,RMVar_hsa_circ_179201,RMVar_hsa_circ_179203,RMVar_hsa_circ_179204,RMVar_hsa_circ_179202,RMVar_hsa_circ_356013,RMVar_hsa_circ_361959,RMVar_hsa_circ_179206,RMVar_hsa_circ_361224,RMVar_hsa_circ_327647,RMVar_hsa_circ_179208 35802 RMVar_ID_35802 Human_SNP_ID_606872083 A-to-I Human chr16 + 68164713 68164713 68164713 CATCCTGGCCAGCATGGTGAAACCCCGTCTCTACTGAAAATACAAAAAAATTAGCCGGGCGTGGT CATCCTGGCCAGCATGGTGAAACCCCGTCTCTCCTGAAAATACAAAAAAATTAGCCGGGCGTGGT A C NFATC3 Ensembl:ENSG00000072736 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1271597737 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_126086 RMVar_hsa_circ_179205,RMVar_hsa_circ_179198,RMVar_hsa_circ_294649,RMVar_hsa_circ_296020,RMVar_hsa_circ_343271,RMVar_hsa_circ_291835,RMVar_hsa_circ_281495,RMVar_hsa_circ_179203,RMVar_hsa_circ_179204,RMVar_hsa_circ_179202,RMVar_hsa_circ_361959,RMVar_hsa_circ_179206,RMVar_hsa_circ_361224,RMVar_hsa_circ_327647,RMVar_hsa_circ_179208,RMVar_hsa_circ_179211,RMVar_hsa_circ_284947,RMVar_hsa_circ_288906,RMVar_hsa_circ_308406,RMVar_hsa_circ_282290,RMVar_hsa_circ_179209,RMVar_hsa_circ_179210,RMVar_hsa_circ_179212 35803 RMVar_ID_35803 Human_SNP_ID_606873070 A-to-I Human chr16 + 68168415 68168414 68168416 GAAATTCTGACTTGAAGTGATCTGCCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG GAAATTCTGACTTGAAGTGATCTGCCCACCTC__CCTCCCAAAGTGCTGGGATTACAGGTGTGAG CAG C NFATC3 Ensembl:ENSG00000072736 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1362953267 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_179205,RMVar_hsa_circ_179198,RMVar_hsa_circ_294649,RMVar_hsa_circ_343271,RMVar_hsa_circ_291835,RMVar_hsa_circ_281495,RMVar_hsa_circ_179203,RMVar_hsa_circ_179204,RMVar_hsa_circ_361959,RMVar_hsa_circ_179206,RMVar_hsa_circ_361224,RMVar_hsa_circ_327647,RMVar_hsa_circ_179208,RMVar_hsa_circ_66224,RMVar_hsa_circ_284947,RMVar_hsa_circ_308406,RMVar_hsa_circ_282290,RMVar_hsa_circ_179209,RMVar_hsa_circ_179210,RMVar_hsa_circ_328864,RMVar_hsa_circ_179212,RMVar_hsa_circ_339036,RMVar_hsa_circ_270108,RMVar_hsa_circ_179213,RMVar_hsa_circ_179214 35804 RMVar_ID_35804 Human_SNP_ID_606873158 A-to-I Human chr16 + 68168688 68168688 68168688 TTGTATTTTTAGTAGAGACGGGGTTTCACCATATTCACCAGGCTAGTCTCGAACTCCTGACCTCG TTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTCACCAGGCTAGTCTCGAACTCCTGACCTCG A G NFATC3 Ensembl:ENSG00000072736 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1435316463 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_179205,RMVar_hsa_circ_179198,RMVar_hsa_circ_294649,RMVar_hsa_circ_343271,RMVar_hsa_circ_291835,RMVar_hsa_circ_281495,RMVar_hsa_circ_179203,RMVar_hsa_circ_179204,RMVar_hsa_circ_361959,RMVar_hsa_circ_179206,RMVar_hsa_circ_361224,RMVar_hsa_circ_327647,RMVar_hsa_circ_179208,RMVar_hsa_circ_66224,RMVar_hsa_circ_284947,RMVar_hsa_circ_308406,RMVar_hsa_circ_282290,RMVar_hsa_circ_179209,RMVar_hsa_circ_179210,RMVar_hsa_circ_328864,RMVar_hsa_circ_179212,RMVar_hsa_circ_339036,RMVar_hsa_circ_270108,RMVar_hsa_circ_179213,RMVar_hsa_circ_179214 35805 RMVar_ID_35805 Human_SNP_ID_606879511 A-to-I Human chr16 + 68193436 68193436 68193436 GCTGTGGTCTCAGTGCTTTGGGAGGCCAAGGTAGGAGGATTACTTGAGACTAGGAGTTTGAGACC GCTGTGGTCTCAGTGCTTTGGGAGGCCAAGGTGGGAGGATTACTTGAGACTAGGAGTTTGAGACC A G NFATC3 Ensembl:ENSG00000072736 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202070107 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12781898,Human_RBP_ID_25221679 RMVar_hsa_circ_53724,RMVar_hsa_circ_343271,RMVar_hsa_circ_66224,RMVar_hsa_circ_346057 35806 RMVar_ID_35806 Human_SNP_ID_606884517 A-to-I Human chr16 + 68213308 68213308 68213308 GTGGTGGCGGGCACCTGTGGTCCCAGGTACTCAGGAGGCTGAGGCAGGAGAATGGCGTGAACTCA GTGGTGGCGGGCACCTGTGGTCCCAGGTACTCGGGAGGCTGAGGCAGGAGAATGGCGTGAACTCA A G NFATC3 Ensembl:ENSG00000072736 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs889350759 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26780541 RMVar_hsa_circ_53724,RMVar_hsa_circ_343271,RMVar_hsa_circ_66224,RMVar_hsa_circ_346057 35807 RMVar_ID_35807 Human_SNP_ID_606887536 A-to-I Human chr16 + 68225046 68225046 68225046 GCAATCTCGGCTCACCGCAACCTCCGCCTCCCAGGTTCAAGTGATTCTCCTGCCTCACCCTCCCG GCAATCTCGGCTCACCGCAACCTCCGCCTCCCGGGTTCAAGTGATTCTCCTGCCTCACCCTCCCG A G AC020978.7,NFATC3 Ensembl:ENSG00000263276,Ensembl:ENSG00000072736 lincRNA,Protein coding exon,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1423849828 Functional Loss SNV dbSNP153 33..33 33 - - - 35808 RMVar_ID_35808 Human_SNP_ID_606887537 A-to-I Human chr16 + 68225052 68225052 68225052 TCGGCTCACCGCAACCTCCGCCTCCCAGGTTCAAGTGATTCTCCTGCCTCACCCTCCCGAGTAGC TCGGCTCACCGCAACCTCCGCCTCCCAGGTTCGAGTGATTCTCCTGCCTCACCCTCCCGAGTAGC A G AC020978.7,NFATC3 Ensembl:ENSG00000263276,Ensembl:ENSG00000072736 lincRNA,Protein coding exon,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs868355240 Functional Loss SNV dbSNP153 33..33 33 - - - 35809 RMVar_ID_35809 Human_SNP_ID_606898682 A-to-I Human chr16 + 68266005 68266005 68266005 TATGCAGGCCGGGCGCGGTGGCTCAGTCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGCGG TATGCAGGCCGGGCGCGGTGGCTCAGTCCTGTGATCCCAGCACTTTGGGAGGCCGAGGCAGGCGG A G SLC7A6 Ensembl:ENSG00000103064 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1199406963 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88143,RMVar_hsa_circ_126841,RMVar_hsa_circ_91429,RMVar_hsa_circ_179228,RMVar_hsa_circ_179229,RMVar_hsa_circ_179227 35810 RMVar_ID_35810 Human_SNP_ID_606900117 A-to-I Human chr16 + 68272354 68272354 68272354 CATGAGGCCGAGATAGAGGACTGCTTGAGCCTAGGAGTTGGAGGCTGCAGTGAGCTATGATTGCA CATGAGGCCGAGATAGAGGACTGCTTGAGCCTGGGAGTTGGAGGCTGCAGTGAGCTATGATTGCA A G SLC7A6 Ensembl:ENSG00000103064 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1403747906 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12782928 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_371452,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_179238,RMVar_hsa_circ_179237,RMVar_hsa_circ_179234,RMVar_hsa_circ_179235,RMVar_hsa_circ_179233,RMVar_hsa_circ_179230,RMVar_hsa_circ_179231 35811 RMVar_ID_35811 Human_SNP_ID_606901217 A-to-I Human chr16 + 68276837 68276834 68276837 CTGGGCAACATGGTGAGACCCTGTCTCTACAAAAAATCAAATTAGCTGGGCATGTTGGTGTGTGC CTGGGCAACATGGTGAGACCCTGTCTCTAC___AAATCAAATTAGCTGGGCATGTTGGTGTGTGC CAAA C SLC7A6 Ensembl:ENSG00000103064 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1261323714 Functional Loss DEL dbSNP153 31..33 33 - - - RMVar_hsa_circ_179232,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_296067,RMVar_hsa_circ_179236,RMVar_hsa_circ_111783,RMVar_hsa_circ_179234,RMVar_hsa_circ_179235,RMVar_hsa_circ_179233,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_362625,RMVar_hsa_circ_179243 35812 RMVar_ID_35812 Human_SNP_ID_606902970 A-to-I Human chr16 + 68284075 68284075 68284075 AGTAGGGTGAGGCAAACGAGGTGCCTGGGGTCAGCGTTGAAGGGCGTACTCACTCTCAGGTTCCG AGTAGGGTGAGGCAAACGAGGTGCCTGGGGTCGGCGTTGAAGGGCGTACTCACTCTCAGGTTCCG A G SLC7A6 Ensembl:ENSG00000103064 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1416074396 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_179232,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_296067,RMVar_hsa_circ_179236,RMVar_hsa_circ_111783,RMVar_hsa_circ_179234,RMVar_hsa_circ_179235,RMVar_hsa_circ_179233,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_362625,RMVar_hsa_circ_179243 35813 RMVar_ID_35813 Human_SNP_ID_606906645 A-to-I Human chr16 + 68298641 68298641 68298641 GTGGGGACTTCTGTTTTCTCCCTGTGGAGATCAGTGAAGACTGGGAGGAAAGCTGCTTCAACCTG GTGGGGACTTCTGTTTTCTCCCTGTGGAGATCGGTGAAGACTGGGAGGAAAGCTGCTTCAACCTG A G SLC7A6 Ensembl:ENSG00000103064 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1038033838 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1520862,Human_RBP_ID_1845041,Human_RBP_ID_8437061,Human_RBP_ID_12783580,Human_RBP_ID_17690673,Human_RBP_ID_17884336,Human_RBP_ID_25222009,Human_RBP_ID_26445265 RMVar_hsa_circ_111783,RMVar_hsa_circ_179230,RMVar_hsa_circ_111921,RMVar_hsa_circ_179241 35814 RMVar_ID_35814 Human_SNP_ID_606907128 A-to-I Human chr16 - 68300741 68300741 68300741 GTCTGAGCAGTGGGAGATTTTAGTTAACAGCTATTTCTGCTTCCAAACTCTGATAACGGTTGTGA GTCTGAGCAGTGGGAGATTTTAGTTAACAGCTGTTTCTGCTTCCAAACTCTGATAACGGTTGTGA T C SLC7A6OS Ensembl:ENSG00000103061 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs781514809 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4379045,Human_RBP_ID_12783715,Human_RBP_ID_26445269 35815 RMVar_ID_35815 Human_SNP_ID_606909331 A-to-I Human chr16 - 68309469 68309469 68309469 CTAGCACGTAGGGAGGCCCAGGCGGGAGGATCACTTGAGCCTGGGGAGGTCAAGGCTACAGTGAG CTAGCACGTAGGGAGGCCCAGGCGGGAGGATCTCTTGAGCCTGGGGAGGTCAAGGCTACAGTGAG T A SLC7A6OS Ensembl:ENSG00000103061 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1252663281 Functional Loss SNV dbSNP153 33..33 33 - - - 35816 RMVar_ID_35816 Human_SNP_ID_606912264 A-to-I Human chr16 + 68318714 68318714 68318714 TGCCACCACACCTGGCTAATATTTGTGTTTTTAGTAGAGACTTGGTTTCACCTGTTGGCCAGGCT TGCCACCACACCTGGCTAATATTTGTGTTTTTCGTAGAGACTTGGTTTCACCTGTTGGCCAGGCT A C PRMT7,AC020978.1 Ensembl:ENSG00000132600,Ensembl:ENSG00000259797 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1406901837 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9345874,Human_RBP_ID_12784032 RMVar_hsa_circ_340373 35817 RMVar_ID_35817 Human_SNP_ID_606913217 A-to-I Human chr16 + 68321996 68321996 68321996 TTGAGACAGAATCTCGCTCTGTCACTCAGGCTAGAGTACAGGGGCGAGATCTCGGCTCACTGCAG TTGAGACAGAATCTCGCTCTGTCACTCAGGCTGGAGTACAGGGGCGAGATCTCGGCTCACTGCAG A G PRMT7 Ensembl:ENSG00000132600 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs577307276 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6528372 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 35818 RMVar_ID_35818 Human_SNP_ID_606913335 A-to-I Human chr16 + 68322400 68322400 68322400 TTGTATGTTTTGTAGAGGCAGAGTTTCGCTGTATTGCCCAGGCTGGTCTTGATCCCCTGAGGTCA TTGTATGTTTTGTAGAGGCAGAGTTTCGCTGTGTTGCCCAGGCTGGTCTTGATCCCCTGAGGTCA A G PRMT7 Ensembl:ENSG00000132600 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1198803593 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6528375,Human_RBP_ID_12784127 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 35819 RMVar_ID_35819 Human_SNP_ID_606913634 A-to-I Human chr16 + 68323420 68323420 68323420 TTTTGTATCTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGTTGGTCTCCAACTCCTGACCT TTTTGTATCTTTAGTAGAGATGGGGTTTCACCGTGTTGGCCAGGTTGGTCTCCAACTCCTGACCT A G PRMT7 Ensembl:ENSG00000132600 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1567649937 Functional Loss SNV dbSNP153 33..33 33 - - - 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 35820 RMVar_ID_35820 Human_SNP_ID_606914388 A-to-I Human chr16 + 68326349 68326349 68326349 TTCACCGCAACCTCCGCCTCCTGGGTTCAAGCAATTCTCTTTTCTCAGCCTCCCAAATAGCTGGG TTCACCGCAACCTCCGCCTCCTGGGTTCAAGCTATTCTCTTTTCTCAGCCTCCCAAATAGCTGGG A T PRMT7 Ensembl:ENSG00000132600 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs957595081 Functional Loss SNV dbSNP153 33..33 33 - - - 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 35821 RMVar_ID_35821 Human_SNP_ID_606914396 A-to-I Human chr16 + 68326372 68326372 68326372 GGTTCAAGCAATTCTCTTTTCTCAGCCTCCCAAATAGCTGGGATTACAGGTATGTACCACTGCAC GGTTCAAGCAATTCTCTTTTCTCAGCCTCCCAGATAGCTGGGATTACAGGTATGTACCACTGCAC A G PRMT7 Ensembl:ENSG00000132600 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs57494306 Functional Loss SNV dbSNP153 33..33 33 - - - 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 35822 RMVar_ID_35822 Human_SNP_ID_606918657 A-to-I Human chr16 + 68342163 68342163 68342163 ACCCGGATGTGGTGGTGCGTGCCTGTAATTCCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCT ACCCGGATGTGGTGGTGCGTGCCTGTAATTCCGGCTACTCGGGAGGCTGAGGCAGGAGAATTGCT A G PRMT7 Ensembl:ENSG00000132600 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1329148765 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85592,RMVar_hsa_circ_94598,RMVar_hsa_circ_91222,RMVar_hsa_circ_30974,RMVar_hsa_circ_179260,RMVar_hsa_circ_179261,RMVar_hsa_circ_179259,RMVar_hsa_circ_42376,RMVar_hsa_circ_365158,RMVar_hsa_circ_118965,RMVar_hsa_circ_179262,RMVar_hsa_circ_179263,RMVar_hsa_circ_377235 35823 RMVar_ID_35823 Human_SNP_ID_606969907 A-to-I Human chr16 + 68540716 68540713 68540717 CCAAGTTGCCAGGTACAGTGGGTCACACCTGTAAGTCCAGCACTTTGGGAAGCTGAGGCAATAGG CCAAGTTGCCAGGTACAGTGGGTCACACCT____GTCCAGCACTTTGGGAAGCTGAGGCAATAGG TGTAA T ZFP90 Ensembl:ENSG00000184939 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1023861265 Functional Loss DEL dbSNP153 31..34 33 - - - 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 35824 RMVar_ID_35824 Human_SNP_ID_606969909 A-to-I Human chr16 + 68540716 68540716 68540716 CCAAGTTGCCAGGTACAGTGGGTCACACCTGTAAGTCCAGCACTTTGGGAAGCTGAGGCAATAGG CCAAGTTGCCAGGTACAGTGGGTCACACCTGTTAGTCCAGCACTTTGGGAAGCTGAGGCAATAGG A T ZFP90 Ensembl:ENSG00000184939 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1461495662 Functional Loss SNV dbSNP153 33..33 33 - - - 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 35825 RMVar_ID_35825 Human_SNP_ID_606971706 A-to-I Human chr16 + 68546535 68546535 68546535 ACAGTATGTTTTGTTTTGTTTTGTTTTTTATTAAGACGGATTCTTGCTCTGTCACCCAGGCTGGA ACAGTATGTTTTGTTTTGTTTTGTTTTTTATTGAGACGGATTCTTGCTCTGTCACCCAGGCTGGA A G ZFP90 Ensembl:ENSG00000184939 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs887980852 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6528470 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 35826 RMVar_ID_35826 Human_SNP_ID_606973777 A-to-I Human chr16 + 68553736 68553736 68553736 GAACTCCCGGGCTCAAGCAGTCCTCCTGCCTCAGCCCTCCAAGTAGCTAGGACCATAGATGCAAG GAACTCCCGGGCTCAAGCAGTCCTCCTGCCTCGGCCCTCCAAGTAGCTAGGACCATAGATGCAAG A G ZFP90 Ensembl:ENSG00000184939 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1211273565 Functional Loss SNV dbSNP153 33..33 33 - - - 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 35827 RMVar_ID_35827 Human_SNP_ID_606974684 A-to-I Human chr16 + 68557190 68557190 68557190 TTTGATCTTTTGTAGAGATGGGGTTTTGCTCTATTGCCTAGGATGGTCTCAAACTCTTGGGCTCC TTTGATCTTTTGTAGAGATGGGGTTTTGCTCTGTTGCCTAGGATGGTCTCAAACTCTTGGGCTCC A G ZFP90 Ensembl:ENSG00000184939 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs753233788 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1732042 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 35828 RMVar_ID_35828 Human_SNP_ID_607009004 A-to-I Human chr16 + 68686345 68686345 68686345 CAGACCGCATGTCTCTCCTTGCGGCGCTACACAAGAGCAGAGTACGAGTCTGAGGTGGAGGGAGT CAGACCGCATGTCTCTCCTTGCGGCGCTACACGAGAGCAGAGTACGAGTCTGAGGTGGAGGGAGT A G CDH3 Ensembl:ENSG00000062038 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs573919158 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_179292,RMVar_hsa_circ_11993,RMVar_hsa_circ_87527,RMVar_hsa_circ_38936,RMVar_hsa_circ_125135,RMVar_hsa_circ_179286,RMVar_hsa_circ_179288,RMVar_hsa_circ_84466,RMVar_hsa_circ_179287,RMVar_hsa_circ_111167,RMVar_hsa_circ_335222,RMVar_hsa_circ_179294,RMVar_hsa_circ_76082,RMVar_hsa_circ_179293 35829 RMVar_ID_35829 Human_SNP_ID_607009005 A-to-I Human chr16 + 68686345 68686345 68686345 CAGACCGCATGTCTCTCCTTGCGGCGCTACACAAGAGCAGAGTACGAGTCTGAGGTGGAGGGAGT CAGACCGCATGTCTCTCCTTGCGGCGCTACACTAGAGCAGAGTACGAGTCTGAGGTGGAGGGAGT A T CDH3 Ensembl:ENSG00000062038 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs573919158 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_179292,RMVar_hsa_circ_11993,RMVar_hsa_circ_87527,RMVar_hsa_circ_38936,RMVar_hsa_circ_125135,RMVar_hsa_circ_179286,RMVar_hsa_circ_179288,RMVar_hsa_circ_84466,RMVar_hsa_circ_179287,RMVar_hsa_circ_111167,RMVar_hsa_circ_335222,RMVar_hsa_circ_179294,RMVar_hsa_circ_76082,RMVar_hsa_circ_179293 35830 RMVar_ID_35830 Human_SNP_ID_607049889 A-to-I Human chr16 + 68836638 68836637 68836639 CCAGCTAATTTTAAAAATTGTTTTGTAGAGACAGGGATCTTGCTATGATGCACAGGCTGGTCTTG CCAGCTAATTTTAAAAATTGTTTTGTAGAGAC__GGATCTTGCTATGATGCACAGGCTGGTCTTG CAG C RF00017-1003 RNACentral:URS0000945854 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1040638608 Functional Loss DEL dbSNP153 33..34 33 - - - 35831 RMVar_ID_35831 Human_SNP_ID_607057616 A-to-I Human chr16 + 68867662 68867662 68867662 AGGAGTTCAAGACCAGCCTGGCCAACATGGTGAATCCCCGTCTCTACTAAAATACAAAAATTAGC AGGAGTTCAAGACCAGCCTGGCCAACATGGTGGATCCCCGTCTCTACTAAAATACAAAAATTAGC A G TANGO6 Ensembl:ENSG00000103047 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs987470836 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19111,RMVar_hsa_circ_40728,RMVar_hsa_circ_322236,RMVar_hsa_circ_345921,RMVar_hsa_circ_368151,RMVar_hsa_circ_377496,RMVar_hsa_circ_364345,RMVar_hsa_circ_339279,RMVar_hsa_circ_297516,RMVar_hsa_circ_89327,RMVar_hsa_circ_179305,RMVar_hsa_circ_179306,RMVar_hsa_circ_179310,RMVar_hsa_circ_109866,RMVar_hsa_circ_369752,RMVar_hsa_circ_179311,RMVar_hsa_circ_286551,RMVar_hsa_circ_29412,RMVar_hsa_circ_31507,RMVar_hsa_circ_21421,RMVar_hsa_circ_179312,RMVar_hsa_circ_179313,RMVar_hsa_circ_179314 35832 RMVar_ID_35832 Human_SNP_ID_607057631 A-to-I Human chr16 + 68867716 68867716 68867716 CAAAAATTAGCCTGGCATGGCGGCGGGCGCCTAACCCCAGCTACTTGGGAGGCTGAGGCAGGAGA CAAAAATTAGCCTGGCATGGCGGCGGGCGCCTCACCCCAGCTACTTGGGAGGCTGAGGCAGGAGA A C TANGO6 Ensembl:ENSG00000103047 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs915091219 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19111,RMVar_hsa_circ_40728,RMVar_hsa_circ_322236,RMVar_hsa_circ_345921,RMVar_hsa_circ_368151,RMVar_hsa_circ_377496,RMVar_hsa_circ_364345,RMVar_hsa_circ_339279,RMVar_hsa_circ_297516,RMVar_hsa_circ_89327,RMVar_hsa_circ_179305,RMVar_hsa_circ_179306,RMVar_hsa_circ_179310,RMVar_hsa_circ_109866,RMVar_hsa_circ_369752,RMVar_hsa_circ_179311,RMVar_hsa_circ_286551,RMVar_hsa_circ_29412,RMVar_hsa_circ_31507,RMVar_hsa_circ_21421,RMVar_hsa_circ_179312,RMVar_hsa_circ_179313,RMVar_hsa_circ_179314 35833 RMVar_ID_35833 Human_SNP_ID_607090603 A-to-I Human chr16 + 69007475 69007475 69007475 GTATTTTTAGTAGAGACGGGTTTCACTGTGTTAGCCAGTATGATCTCGATCTGACCTCATGATCC GTATTTTTAGTAGAGACGGGTTTCACTGTGTTGGCCAGTATGATCTCGATCTGACCTCATGATCC A G TANGO6 Ensembl:ENSG00000103047 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs916850552 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79117,RMVar_hsa_circ_179319,RMVar_hsa_circ_54710,RMVar_hsa_circ_90579,RMVar_hsa_circ_121273,RMVar_hsa_circ_179322,RMVar_hsa_circ_179323,RMVar_hsa_circ_353122,RMVar_hsa_circ_360700,RMVar_hsa_circ_347010,RMVar_hsa_circ_360242,RMVar_hsa_circ_179328 35834 RMVar_ID_35834 Human_SNP_ID_607100444 A-to-I Human chr16 + 69049487 69049486 69049487 AAGTTTCGCTCTTGTCCCCCAAGCTGGTGTACAATGGCGCCATCTCGTCTCACTGCAACCTCTGC AAGTTTCGCTCTTGTCCCCCAAGCTGGTGTAC_ATGGCGCCATCTCGTCTCACTGCAACCTCTGC CA C TANGO6 Ensembl:ENSG00000103047 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1371827016 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_90579,RMVar_hsa_circ_179323 35835 RMVar_ID_35835 Human_SNP_ID_607101927 A-to-I Human chr16 + 69055892 69055892 69055892 AGCCCTTTCTCTACTGAAAATACCAAAAAATTAGCCGGGAGTGGTGGTGGGCGTCTGTAATCCCA AGCCCTTTCTCTACTGAAAATACCAAAAAATTCGCCGGGAGTGGTGGTGGGCGTCTGTAATCCCA A C TANGO6 Ensembl:ENSG00000103047 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348301223 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90579,RMVar_hsa_circ_179323 35836 RMVar_ID_35836 Human_SNP_ID_607109546 A-to-I Human chr16 + 69085966 69085966 69085966 ATGGCTCACTGCAGCCTTGACCTCCTGGGCTCAAGGAATTCTCCCACCTCAGCACCCCCGAGTAG ATGGCTCACTGCAGCCTTGACCTCCTGGGCTCGAGGAATTCTCCCACCTCAGCACCCCCGAGTAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs192215799 Functional Loss SNV dbSNP153 33..33 33 - - - 35837 RMVar_ID_35837 Human_SNP_ID_607119819 A-to-I Human chr16 - 69122815 69122815 69122815 AAATTAAGCCAGGTGCGGTGGTTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAAGTGGGTGG AAATTAAGCCAGGTGCGGTGGTTCACGCCTGTCATCCCAGCACTTTGGGAGGCCAAAGTGGGTGG T G DERPC,CHTF8 Ensembl:ENSG00000286140,Ensembl:ENSG00000168802 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1375380863 Functional Loss SNV dbSNP153 33..33 33 - - - 35838 RMVar_ID_35838 Human_SNP_ID_607120010 A-to-I Human chr16 - 69123557 69123557 69123557 GCCTCCCAGGGTTCAAGTGATTCTCTTACCTCAGCCTGCCGAATAGCTGGGATTATGGGTGCCTG GCCTCCCAGGGTTCAAGTGATTCTCTTACCTCGGCCTGCCGAATAGCTGGGATTATGGGTGCCTG T C DERPC,CHTF8 Ensembl:ENSG00000286140,Ensembl:ENSG00000168802 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1230922866 Functional Loss SNV dbSNP153 33..33 33 - - - 35839 RMVar_ID_35839 Human_SNP_ID_607120039 A-to-I Human chr16 - 69123644 69123644 69123644 TTGGATTTATTGATTGATTGATTGATTTTTTGAGACAGTCTCACTCTGTCGCCCAGGGTGGAGCA TTGGATTTATTGATTGATTGATTGATTTTTTGGGACAGTCTCACTCTGTCGCCCAGGGTGGAGCA T C DERPC,CHTF8 Ensembl:ENSG00000286140,Ensembl:ENSG00000168802 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs964387366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12785322 35840 RMVar_ID_35840 Human_SNP_ID_607120981 A-to-I Human chr16 - 69126990 69126990 69126990 TGCCCACCTTGGCCTCCCAAAGTGCTGAGATTACAGGCATGAGCCACCGCGCCCGGCCTCATACA TGCCCACCTTGGCCTCCCAAAGTGCTGAGATTGCAGGCATGAGCCACCGCGCCCGGCCTCATACA T C DERPC,CHTF8 Ensembl:ENSG00000286140,Ensembl:ENSG00000168802 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs761290438 Functional Loss SNV dbSNP153 33..33 33 - - - 35841 RMVar_ID_35841 Human_SNP_ID_607121213 A-to-I Human chr16 - 69127685 69127685 69127685 GAATCACTTGAACCTGGGAGACAGAGGTTGCAATGAGCTGAGATCGAGCCACTGCACTCCAGCCT GAATCACTTGAACCTGGGAGACAGAGGTTGCAGTGAGCTGAGATCGAGCCACTGCACTCCAGCCT T C DERPC,CHTF8 Ensembl:ENSG00000286140,Ensembl:ENSG00000168802 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1452269937 Functional Loss SNV dbSNP153 33..33 33 - - - 35842 RMVar_ID_35842 Human_SNP_ID_607123616 A-to-I Human chr16 + 69135531 69135531 69135531 GCCCAGGAGTGTAAGACCACCCTGGGCAACATAGTGAGACCCCATCCCTAAAAAAATAAATAAAT GCCCAGGAGTGTAAGACCACCCTGGGCAACATGGTGAGACCCCATCCCTAAAAAAATAAATAAAT A G UTP4 Ensembl:ENSG00000141076 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1280586740 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123142,RMVar_hsa_circ_38462,RMVar_hsa_circ_179331,RMVar_hsa_circ_357278 35843 RMVar_ID_35843 Human_SNP_ID_607124446 A-to-I Human chr16 + 69138255 69138255 69138255 GTTCTTTTCTTTCTTTTTTTTTTTTTTTCTGGAGGCAGAGTGTCACTCTGTCATCCATGCTGGCA GTTCTTTTCTTTCTTTTTTTTTTTTTTTCTGGGGGCAGAGTGTCACTCTGTCATCCATGCTGGCA A G UTP4 Ensembl:ENSG00000141076 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1182004208 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_44966,Human_RBP_ID_233794,Human_RBP_ID_761524,Human_RBP_ID_6528866,Human_RBP_ID_9833060,Human_RBP_ID_12868436,Human_RBP_ID_22946206,Human_RBP_ID_23307679 RMVar_hsa_circ_34831,RMVar_hsa_circ_123142,RMVar_hsa_circ_296623,RMVar_hsa_circ_38462,RMVar_hsa_circ_179331,RMVar_hsa_circ_339130,RMVar_hsa_circ_346703,RMVar_hsa_circ_51333,RMVar_hsa_circ_279753,RMVar_hsa_circ_48822,RMVar_hsa_circ_111704,RMVar_hsa_circ_179333,RMVar_hsa_circ_179335,RMVar_hsa_circ_6404,RMVar_hsa_circ_179334,RMVar_hsa_circ_179332,RMVar_hsa_circ_179337,RMVar_hsa_circ_94727,RMVar_hsa_circ_179336 35844 RMVar_ID_35844 Human_SNP_ID_607124726 A-to-I Human chr16 + 69139108 69139108 69139108 CTCCTGCCTCAGCCTCCCTAGTAGCTGGGACTACAGGTGCGTGCCACCATGCCCGGCTAGTTTTT CTCCTGCCTCAGCCTCCCTAGTAGCTGGGACTGCAGGTGCGTGCCACCATGCCCGGCTAGTTTTT A G UTP4 Ensembl:ENSG00000141076 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1407576871 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1732791 RMVar_hsa_circ_34831,RMVar_hsa_circ_123142,RMVar_hsa_circ_296623,RMVar_hsa_circ_38462,RMVar_hsa_circ_179331,RMVar_hsa_circ_339130,RMVar_hsa_circ_346703,RMVar_hsa_circ_51333,RMVar_hsa_circ_279753,RMVar_hsa_circ_48822,RMVar_hsa_circ_111704,RMVar_hsa_circ_179333,RMVar_hsa_circ_179335,RMVar_hsa_circ_6404,RMVar_hsa_circ_179334,RMVar_hsa_circ_179332,RMVar_hsa_circ_179337,RMVar_hsa_circ_94727,RMVar_hsa_circ_179336 35845 RMVar_ID_35845 Human_SNP_ID_607124736 A-to-I Human chr16 + 69139134 69139134 69139134 GGGACTACAGGTGCGTGCCACCATGCCCGGCTAGTTTTTGTGTTTTTAGTAGAGACGGGGTTTCA GGGACTACAGGTGCGTGCCACCATGCCCGGCTGGTTTTTGTGTTTTTAGTAGAGACGGGGTTTCA A G UTP4 Ensembl:ENSG00000141076 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1316732097 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34831,RMVar_hsa_circ_123142,RMVar_hsa_circ_296623,RMVar_hsa_circ_38462,RMVar_hsa_circ_179331,RMVar_hsa_circ_339130,RMVar_hsa_circ_346703,RMVar_hsa_circ_51333,RMVar_hsa_circ_279753,RMVar_hsa_circ_48822,RMVar_hsa_circ_111704,RMVar_hsa_circ_179333,RMVar_hsa_circ_179335,RMVar_hsa_circ_6404,RMVar_hsa_circ_179334,RMVar_hsa_circ_179332,RMVar_hsa_circ_179337,RMVar_hsa_circ_94727,RMVar_hsa_circ_179336 35846 RMVar_ID_35846 Human_SNP_ID_607124740 A-to-I Human chr16 + 69139152 69139152 69139152 CACCATGCCCGGCTAGTTTTTGTGTTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGG CACCATGCCCGGCTAGTTTTTGTGTTTTTAGTGGAGACGGGGTTTCACCATGTTGGCCAGGCTGG A G UTP4 Ensembl:ENSG00000141076 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1280886081 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34831,RMVar_hsa_circ_123142,RMVar_hsa_circ_296623,RMVar_hsa_circ_38462,RMVar_hsa_circ_179331,RMVar_hsa_circ_339130,RMVar_hsa_circ_346703,RMVar_hsa_circ_51333,RMVar_hsa_circ_279753,RMVar_hsa_circ_48822,RMVar_hsa_circ_111704,RMVar_hsa_circ_179333,RMVar_hsa_circ_179335,RMVar_hsa_circ_6404,RMVar_hsa_circ_179334,RMVar_hsa_circ_179332,RMVar_hsa_circ_179337,RMVar_hsa_circ_94727,RMVar_hsa_circ_179336 35847 RMVar_ID_35847 Human_SNP_ID_607126524 A-to-I Human chr16 + 69145338 69145338 69145338 GCTGGAGTGCAGTGGTGCAGTCTCGGCTCACTACAACCTCTGTCTCCTGGGTTCAAGCGATTCTC GCTGGAGTGCAGTGGTGCAGTCTCGGCTCACTGCAACCTCTGTCTCCTGGGTTCAAGCGATTCTC A G UTP4 Ensembl:ENSG00000141076 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1262936382 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34831,RMVar_hsa_circ_123142,RMVar_hsa_circ_38462,RMVar_hsa_circ_179331,RMVar_hsa_circ_339130,RMVar_hsa_circ_346703,RMVar_hsa_circ_51333,RMVar_hsa_circ_48822,RMVar_hsa_circ_111704,RMVar_hsa_circ_179333,RMVar_hsa_circ_6404,RMVar_hsa_circ_179334,RMVar_hsa_circ_179332,RMVar_hsa_circ_179337,RMVar_hsa_circ_376750,RMVar_hsa_circ_333271,RMVar_hsa_circ_22941,RMVar_hsa_circ_78632,RMVar_hsa_circ_274864,RMVar_hsa_circ_39077,RMVar_hsa_circ_179340,RMVar_hsa_circ_179341,RMVar_hsa_circ_179342,RMVar_hsa_circ_282951,RMVar_hsa_circ_325328,RMVar_hsa_circ_108003,RMVar_hsa_circ_179343 35848 RMVar_ID_35848 Human_SNP_ID_607127193 A-to-I Human chr16 + 69147384 69147384 69147384 AAAATTAGCTGGGCGTGGCGGTATGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTAGCTGGGCGTGGCGGTATGCGCCTGTCGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA A C UTP4 Ensembl:ENSG00000141076 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs766671017 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34831,RMVar_hsa_circ_123142,RMVar_hsa_circ_38462,RMVar_hsa_circ_179331,RMVar_hsa_circ_339130,RMVar_hsa_circ_346703,RMVar_hsa_circ_51333,RMVar_hsa_circ_48822,RMVar_hsa_circ_111704,RMVar_hsa_circ_179333,RMVar_hsa_circ_6404,RMVar_hsa_circ_179334,RMVar_hsa_circ_179332,RMVar_hsa_circ_179337,RMVar_hsa_circ_376750,RMVar_hsa_circ_333271,RMVar_hsa_circ_22941,RMVar_hsa_circ_78632,RMVar_hsa_circ_274864,RMVar_hsa_circ_39077,RMVar_hsa_circ_179340,RMVar_hsa_circ_179341,RMVar_hsa_circ_179342,RMVar_hsa_circ_282951,RMVar_hsa_circ_325328,RMVar_hsa_circ_108003,RMVar_hsa_circ_179343 35849 RMVar_ID_35849 Human_SNP_ID_607130605 A-to-I Human chr16 + 69158438 69158438 69158438 CTCCTGCCTCAGCCTCCCAAAGTGCTAGGATTACAGGTGTGAGTCACCATGCCTAGTGAAAGTCA CTCCTGCCTCAGCCTCCCAAAGTGCTAGGATTGCAGGTGTGAGTCACCATGCCTAGTGAAAGTCA A G UTP4 Ensembl:ENSG00000141076 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1289479224 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38462,RMVar_hsa_circ_51333,RMVar_hsa_circ_111704,RMVar_hsa_circ_6404,RMVar_hsa_circ_179337,RMVar_hsa_circ_333271,RMVar_hsa_circ_78632,RMVar_hsa_circ_179342,RMVar_hsa_circ_116527,RMVar_hsa_circ_87595,RMVar_hsa_circ_179348,RMVar_hsa_circ_179349,RMVar_hsa_circ_120977,RMVar_hsa_circ_64992,RMVar_hsa_circ_179353,RMVar_hsa_circ_179352,RMVar_hsa_circ_79053,RMVar_hsa_circ_179351,RMVar_hsa_circ_125580,RMVar_hsa_circ_314470,RMVar_hsa_circ_374973,RMVar_hsa_circ_377000,RMVar_hsa_circ_284171,RMVar_hsa_circ_17433,RMVar_hsa_circ_179355,RMVar_hsa_circ_179356,RMVar_hsa_circ_179357,RMVar_hsa_circ_179354 35850 RMVar_ID_35850 Human_SNP_ID_607130857 A-to-I Human chr16 + 69159478 69159478 69159478 TTTGGAGGCCGAGGTGGGCAGATCATAAGGTCAAGAGATCGAGACCATGCTGACCAAAATGGTGA TTTGGAGGCCGAGGTGGGCAGATCATAAGGTCGAGAGATCGAGACCATGCTGACCAAAATGGTGA A G UTP4 Ensembl:ENSG00000141076 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1012012968 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38462,RMVar_hsa_circ_51333,RMVar_hsa_circ_111704,RMVar_hsa_circ_6404,RMVar_hsa_circ_179337,RMVar_hsa_circ_333271,RMVar_hsa_circ_78632,RMVar_hsa_circ_179342,RMVar_hsa_circ_116527,RMVar_hsa_circ_87595,RMVar_hsa_circ_179348,RMVar_hsa_circ_179349,RMVar_hsa_circ_120977,RMVar_hsa_circ_64992,RMVar_hsa_circ_179353,RMVar_hsa_circ_179352,RMVar_hsa_circ_79053,RMVar_hsa_circ_179351,RMVar_hsa_circ_125580,RMVar_hsa_circ_314470,RMVar_hsa_circ_374973,RMVar_hsa_circ_377000,RMVar_hsa_circ_284171,RMVar_hsa_circ_17433,RMVar_hsa_circ_179355,RMVar_hsa_circ_179356,RMVar_hsa_circ_179357,RMVar_hsa_circ_179354 35851 RMVar_ID_35851 Human_SNP_ID_607131511 A-to-I Human chr16 + 69161825 69161825 69161825 AGCTGGGACTACAGGCGAGTCCCACCACACCTAGCTAATCTTTTTTTTTAGTAGAGATGAGGTTT AGCTGGGACTACAGGCGAGTCCCACCACACCTCGCTAATCTTTTTTTTTAGTAGAGATGAGGTTT A C UTP4 Ensembl:ENSG00000141076 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1414642527 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12786097 RMVar_hsa_circ_1476,RMVar_hsa_circ_38462,RMVar_hsa_circ_51333,RMVar_hsa_circ_111704,RMVar_hsa_circ_6404,RMVar_hsa_circ_179337,RMVar_hsa_circ_333271,RMVar_hsa_circ_78632,RMVar_hsa_circ_179342,RMVar_hsa_circ_87595,RMVar_hsa_circ_179349,RMVar_hsa_circ_120977,RMVar_hsa_circ_179353,RMVar_hsa_circ_179352,RMVar_hsa_circ_125580,RMVar_hsa_circ_314470,RMVar_hsa_circ_374973,RMVar_hsa_circ_377000,RMVar_hsa_circ_284171,RMVar_hsa_circ_17433,RMVar_hsa_circ_179355,RMVar_hsa_circ_179356,RMVar_hsa_circ_179357,RMVar_hsa_circ_179354,RMVar_hsa_circ_271008,RMVar_hsa_circ_300664,RMVar_hsa_circ_179360,RMVar_hsa_circ_179361,RMVar_hsa_circ_179359 35852 RMVar_ID_35852 Human_SNP_ID_607131532 A-to-I Human chr16 + 69161896 69161896 69161896 GTTGCCCAGGCTGGTCTTGAACTCCTGGACTCAAGCGTTCCTCCCGCCCTGGCCCTTCCGAAGTG GTTGCCCAGGCTGGTCTTGAACTCCTGGACTCCAGCGTTCCTCCCGCCCTGGCCCTTCCGAAGTG A C UTP4 Ensembl:ENSG00000141076 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1293684300 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1476,RMVar_hsa_circ_38462,RMVar_hsa_circ_51333,RMVar_hsa_circ_111704,RMVar_hsa_circ_6404,RMVar_hsa_circ_179337,RMVar_hsa_circ_333271,RMVar_hsa_circ_78632,RMVar_hsa_circ_179342,RMVar_hsa_circ_87595,RMVar_hsa_circ_179349,RMVar_hsa_circ_120977,RMVar_hsa_circ_179353,RMVar_hsa_circ_179352,RMVar_hsa_circ_125580,RMVar_hsa_circ_314470,RMVar_hsa_circ_374973,RMVar_hsa_circ_377000,RMVar_hsa_circ_284171,RMVar_hsa_circ_17433,RMVar_hsa_circ_179355,RMVar_hsa_circ_179356,RMVar_hsa_circ_179357,RMVar_hsa_circ_179354,RMVar_hsa_circ_271008,RMVar_hsa_circ_300664,RMVar_hsa_circ_179360,RMVar_hsa_circ_179361,RMVar_hsa_circ_179359 35853 RMVar_ID_35853 Human_SNP_ID_607131690 A-to-I Human chr16 + 69162394 69162394 69162394 GGTCAGAAGTTCAAAACCAGCCCGGCCAACATAGTGAGACCCCGTTTCTACTAAAAATACAAAAA GGTCAGAAGTTCAAAACCAGCCCGGCCAACATGGTGAGACCCCGTTTCTACTAAAAATACAAAAA A G UTP4 Ensembl:ENSG00000141076 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1029367574 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1476,RMVar_hsa_circ_38462,RMVar_hsa_circ_51333,RMVar_hsa_circ_111704,RMVar_hsa_circ_6404,RMVar_hsa_circ_179337,RMVar_hsa_circ_333271,RMVar_hsa_circ_78632,RMVar_hsa_circ_179342,RMVar_hsa_circ_87595,RMVar_hsa_circ_179349,RMVar_hsa_circ_120977,RMVar_hsa_circ_179353,RMVar_hsa_circ_179352,RMVar_hsa_circ_125580,RMVar_hsa_circ_314470,RMVar_hsa_circ_374973,RMVar_hsa_circ_377000,RMVar_hsa_circ_284171,RMVar_hsa_circ_17433,RMVar_hsa_circ_179355,RMVar_hsa_circ_179356,RMVar_hsa_circ_179357,RMVar_hsa_circ_179354,RMVar_hsa_circ_271008,RMVar_hsa_circ_300664,RMVar_hsa_circ_179360,RMVar_hsa_circ_179361,RMVar_hsa_circ_179359 35854 RMVar_ID_35854 Human_SNP_ID_607134592 A-to-I Human chr16 + 69172439 69172439 69172439 CACCACGCCCGGCTAATTTTTTGTATTTTAGTAGAGACGGGGTTTCAGCATGTTGGCCAGGATGG CACCACGCCCGGCTAATTTTTTGTATTTTAGTGGAGACGGGGTTTCAGCATGTTGGCCAGGATGG A G UTP4 Ensembl:ENSG00000141076 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1259399725 Functional Loss SNV dbSNP153 33..33 33 - - - 35855 RMVar_ID_35855 Human_SNP_ID_607144253 A-to-I Human chr16 + 69209223 69209223 69209223 TCGATCTCCTGACCTCATGATCCGCCTGCCTCAGCCTCCCAAAGTGCCTGGCCACCATGCCTGGC TCGATCTCCTGACCTCATGATCCGCCTGCCTCTGCCTCCCAAAGTGCCTGGCCACCATGCCTGGC A T UTP4,SNTB2 Ensembl:ENSG00000141076,Ensembl:ENSG00000168807 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910372865 Functional Loss SNV dbSNP153 33..33 33 - - - 35856 RMVar_ID_35856 Human_SNP_ID_607158455 A-to-I Human chr16 + 69266856 69266856 69266856 CTCCCACCTCAGTCTCCTGAGTCGCTGGGACTACAGATGCACACCATCATGCCTGGCTGATTTTC CTCCCACCTCAGTCTCCTGAGTCGCTGGGACTGCAGATGCACACCATCATGCCTGGCTGATTTTC A G SNTB2 Ensembl:ENSG00000168807 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1378704238 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_179368,RMVar_hsa_circ_179369,RMVar_hsa_circ_12805,RMVar_hsa_circ_179373,RMVar_hsa_circ_271303,RMVar_hsa_circ_271404,RMVar_hsa_circ_110385,RMVar_hsa_circ_179374,RMVar_hsa_circ_179372,RMVar_hsa_circ_325927,RMVar_hsa_circ_283688 35857 RMVar_ID_35857 Human_SNP_ID_607163582 A-to-I Human chr16 + 69286578 69286578 69286578 GTGGTGACACACATCTGTAGCCCCAGCTACTCAGGAGGCTGAGGTAGGAGGATCACCTGAGCCCA GTGGTGACACACATCTGTAGCCCCAGCTACTCGGGAGGCTGAGGTAGGAGGATCACCTGAGCCCA A G SNTB2 Ensembl:ENSG00000168807 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1220541552 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12805,RMVar_hsa_circ_110385,RMVar_hsa_circ_179374,RMVar_hsa_circ_104695,RMVar_hsa_circ_179375,RMVar_hsa_circ_309792,RMVar_hsa_circ_179379 35858 RMVar_ID_35858 Human_SNP_ID_607167873 A-to-I Human chr16 + 69303050 69303050 69303050 CACCACACCCAGCTAATTTTTGTATTTTTAGTAGAGGCAGGTTTTCACCATGTTGGCTAGGCTGG CACCACACCCAGCTAATTTTTGTATTTTTAGTGGAGGCAGGTTTTCACCATGTTGGCTAGGCTGG A G SNTB2,AC026464.4 Ensembl:ENSG00000168807,Ensembl:ENSG00000260914 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1440474269 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12877581 35859 RMVar_ID_35859 Human_SNP_ID_607168197 A-to-I Human chr16 + 69304695 69304663 69304695 TTTTCCTTCTTTTTTTTTTGAGACAGGTTCTCACTCTGTCACCGAGGTTGGAGTGCAGTGGTATG T________________________________CTCTGTCACCGAGGTTGGAGTGCAGTGGTATG TTTTCCTTCTTTTTTTTTTGAGACAGGTTCTCA T SNTB2,AC026464.4 Ensembl:ENSG00000168807,Ensembl:ENSG00000260914 Protein coding,Protein coding 3'UTR,intron GSE100210;GSE107867 HepG2 cell line;ASD brains,frontal_cortex - 29129909,30559470 RNA-Seq:(High) rs1458427695 Functional Loss DEL dbSNP153 2..33 33 - - - Human_RBP_ID_12786967,Human_RBP_ID_23697202 Human_miRNA_ID_866987,Human_miRNA_ID_1793043 35860 RMVar_ID_35860 Human_SNP_ID_607168208 A-to-I Human chr16 + 69304695 69304691 69304695 TTTTCCTTCTTTTTTTTTTGAGACAGGTTCTCACTCTGTCACCGAGGTTGGAGTGCAGTGGTATG TTTTCCTTCTTTTTTTTTTGAGACAGGTT____CTCTGTCACCGAGGTTGGAGTGCAGTGGTATG TCTCA T SNTB2,AC026464.4 Ensembl:ENSG00000168807,Ensembl:ENSG00000260914 Protein coding,Protein coding 3'UTR,intron GSE100210;GSE107867 HepG2 cell line;ASD brains,frontal_cortex - 29129909,30559470 RNA-Seq:(High) rs1190948988 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_12786967,Human_RBP_ID_23697202 Human_miRNA_ID_866987,Human_miRNA_ID_1793043 35861 RMVar_ID_35861 Human_SNP_ID_607168606 A-to-I Human chr16 + 69306725 69306725 69306725 TGGGAGCCCAAGGTGGGTGGATCACCTGAGGTAAGGAGTTTGAGACCAGCCTGGCCAACATGGTG TGGGAGCCCAAGGTGGGTGGATCACCTGAGGTGAGGAGTTTGAGACCAGCCTGGCCAACATGGTG A G SNTB2,AC026464.4 Ensembl:ENSG00000168807,Ensembl:ENSG00000260914 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251689938 Functional Loss SNV dbSNP153 33..33 33 - - - 35862 RMVar_ID_35862 Human_SNP_ID_607170611 A-to-I Human chr16 - 69314142 69314142 69314142 GCTAACACAGTGAAGCACCATCTCTACTAAAAATACAAAAAGTTAGCCGGGTGTGGTGACGCGTG GCTAACACAGTGAAGCACCATCTCTACTAAAAGTACAAAAAGTTAGCCGGGTGTGGTGACGCGTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1036021757 Functional Loss SNV dbSNP153 33..33 33 - - - 35863 RMVar_ID_35863 Human_SNP_ID_607171857 A-to-I Human chr16 + 69318225 69318213 69318226 AAACTCCTGGGCTCAAGCGATCCTCCCGCCTCAGCCTCCCAGAGTGCTGGGATTACAGGGGTGAG AAACTCCTGGGCTCAAGCGAT_____________CCTCCCAGAGTGCTGGGATTACAGGGGTGAG TCCTCCCGCCTCAG T VPS4A,AC026464.4 Ensembl:ENSG00000132612,Ensembl:ENSG00000260914 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1261687904 Functional Loss DEL dbSNP153 22..34 33 - - - 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_76611,RMVar_hsa_circ_25976,RMVar_hsa_circ_59180,RMVar_hsa_circ_179385,RMVar_hsa_circ_179386,RMVar_hsa_circ_179387 35864 RMVar_ID_35864 Human_SNP_ID_607173646 A-to-I Human chr16 - 69322857 69322857 69322857 CTCCATATTGGCTAGGCTGGTCTCGAACTCCTAACCTTGTGATCTGCCCACCCTGGCCTCCCAAA CTCCATATTGGCTAGGCTGGTCTCGAACTCCTGACCTTGTGATCTGCCCACCCTGGCCTCCCAAA T C COG8 Ensembl:ENSG00000213380 Protein coding intron GSE107867;GSE126723:GSM3611830,GSM3611831,GSM3611832 ASD brains,frontal_cortex;Bronchiolar epithelium,BERP35T1 cell line - 30559470,31158229 RNA-Seq:(High) rs573801622 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4379692,Human_RBP_ID_12787379 35865 RMVar_ID_35865 Human_SNP_ID_607173662 A-to-I Human chr16 - 69322911 69322911 69322911 AGTGCACACCACCACACCCGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCTCCATATTGG AGTGCACACCACCACACCCGGCTAATTTTTGTGTTTTTAGTAGAGACAGGGTTTCTCCATATTGG T C COG8 Ensembl:ENSG00000213380 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs544928045 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12787382 35866 RMVar_ID_35866 Human_SNP_ID_607173688 A-to-I Human chr16 - 69323021 69323021 69323021 CTCTGTCACCCAGGCTGGAGTGCAGTGGCCCAATCTCTGCTCACTGCAACCTCTGCCTCCCGGCT CTCTGTCACCCAGGCTGGAGTGCAGTGGCCCAGTCTCTGCTCACTGCAACCTCTGCCTCCCGGCT T C COG8 Ensembl:ENSG00000213380 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1194248563 Functional Loss SNV dbSNP153 33..33 33 - - - 35867 RMVar_ID_35867 Human_SNP_ID_607173771 A-to-I Human chr16 - 69323285 69323285 69323285 TTAGCTGGGCATGATGGTGTGTGCCTGTTGCTACTCAGGAGGCTGAGGTCAGAAGATTGTGTGAG TTAGCTGGGCATGATGGTGTGTGCCTGTTGCTGCTCAGGAGGCTGAGGTCAGAAGATTGTGTGAG T C COG8 Ensembl:ENSG00000213380 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1446367516 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1845214,Human_RBP_ID_6529410,Human_RBP_ID_12787393,Human_RBP_ID_18286780 35868 RMVar_ID_35868 Human_SNP_ID_607173822 A-to-I Human chr16 - 69323470 69323470 69323470 GTCATATTATCTGGACCTGACTTTACTTGCTAAAGAATATAAAATGCAGGCTAGGTGTGGTGGCT GTCATATTATCTGGACCTGACTTTACTTGCTACAGAATATAAAATGCAGGCTAGGTGTGGTGGCT T G COG8 Ensembl:ENSG00000213380 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992657539 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_478309,Human_RBP_ID_1845216,Human_RBP_ID_3498049,Human_RBP_ID_4379703,Human_RBP_ID_8083818,Human_RBP_ID_8809404,Human_RBP_ID_12787412,Human_RBP_ID_22946210,Human_RBP_ID_27659813 35869 RMVar_ID_35869 Human_SNP_ID_607173823 A-to-I Human chr16 - 69323471 69323471 69323471 CGTCATATTATCTGGACCTGACTTTACTTGCTAAAGAATATAAAATGCAGGCTAGGTGTGGTGGC CGTCATATTATCTGGACCTGACTTTACTTGCTGAAGAATATAAAATGCAGGCTAGGTGTGGTGGC T C COG8 Ensembl:ENSG00000213380 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1294159196 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_478309,Human_RBP_ID_1845216,Human_RBP_ID_3498049,Human_RBP_ID_4379703,Human_RBP_ID_8083818,Human_RBP_ID_8809404,Human_RBP_ID_12787412,Human_RBP_ID_22946210,Human_RBP_ID_27659813 35870 RMVar_ID_35870 Human_SNP_ID_607174746 A-to-I Human chr16 - 69325554 69325554 69325554 TAATTTTTTTATTTTTAGTGAGACGGGGTTTCACTGTGTTAGCCAGGATGTTCTCGATTTCCTGA TAATTTTTTTATTTTTAGTGAGACGGGGTTTCGCTGTGTTAGCCAGGATGTTCTCGATTTCCTGA T C COG8 Ensembl:ENSG00000213380 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1414705052 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6529470,Human_RBP_ID_18682702 35871 RMVar_ID_35871 Human_SNP_ID_607174752 A-to-I Human chr16 - 69325570 69325570 69325570 CACCACCACGCCCGGCTAATTTTTTTATTTTTAGTGAGACGGGGTTTCACTGTGTTAGCCAGGAT CACCACCACGCCCGGCTAATTTTTTTATTTTTGGTGAGACGGGGTTTCACTGTGTTAGCCAGGAT T C COG8 Ensembl:ENSG00000213380 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202435510 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4379771,Human_RBP_ID_6529470,Human_RBP_ID_12787562,Human_RBP_ID_18286793,Human_RBP_ID_18682702 35872 RMVar_ID_35872 Human_SNP_ID_607175345 A-to-I Human chr16 - 69327296 69327296 69327296 GGGTGTGCTGGTAGGCGCCTGTAATCACAGCTACTTGGGAGGCTGAGGCGGGAGAATCGCTCAAA GGGTGTGCTGGTAGGCGCCTGTAATCACAGCTGCTTGGGAGGCTGAGGCGGGAGAATCGCTCAAA T C PDF,COG8 Ensembl:ENSG00000258429,Ensembl:ENSG00000213380 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1045557542 Functional Loss SNV dbSNP153 33..33 33 - - - 35873 RMVar_ID_35873 Human_SNP_ID_607175363 A-to-I Human chr16 - 69327335 69327335 69327335 GGCGAAACACTGTTTCTACTAAAAATATGAAAATTAGCTGGGTGTGCTGGTAGGCGCCTGTAATC GGCGAAACACTGTTTCTACTAAAAATATGAAAGTTAGCTGGGTGTGCTGGTAGGCGCCTGTAATC T C PDF,COG8 Ensembl:ENSG00000258429,Ensembl:ENSG00000213380 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1316978213 Functional Loss SNV dbSNP153 33..33 33 - - - 35874 RMVar_ID_35874 Human_SNP_ID_607175367 A-to-I Human chr16 - 69327341 69327341 69327341 CAACATGGCGAAACACTGTTTCTACTAAAAATATGAAAATTAGCTGGGTGTGCTGGTAGGCGCCT CAACATGGCGAAACACTGTTTCTACTAAAAATGTGAAAATTAGCTGGGTGTGCTGGTAGGCGCCT T C PDF,COG8 Ensembl:ENSG00000258429,Ensembl:ENSG00000213380 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs996727369 Functional Loss SNV dbSNP153 33..33 33 - - - 35875 RMVar_ID_35875 Human_SNP_ID_607175579 A-to-I Human chr16 - 69328068 69328068 69328068 TGGCGAGCACCTGTAATCCCAGCTACTCGTGAAGCCAAGGCAGAGAATTACTTGAACCCAGGAGG TGGCGAGCACCTGTAATCCCAGCTACTCGTGAGGCCAAGGCAGAGAATTACTTGAACCCAGGAGG T C PDF,COG8 Ensembl:ENSG00000258429,Ensembl:ENSG00000213380 Protein coding,Protein coding 3'UTR,intron GSE38233;GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1164465279 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1521135,Human_RBP_ID_2480187,Human_RBP_ID_3498059,Human_RBP_ID_6529553,Human_RBP_ID_8437405,Human_RBP_ID_12787691,Human_RBP_ID_17690711,Human_RBP_ID_27444644 35876 RMVar_ID_35876 Human_SNP_ID_607175623 A-to-I Human chr16 - 69328183 69328183 69328183 CCAGCACTTTGGGAGGGCGGGGCGGGTGGATCACGAGGTCAGGAGCTCAAGACCAGCCTGGCCAA CCAGCACTTTGGGAGGGCGGGGCGGGTGGATCGCGAGGTCAGGAGCTCAAGACCAGCCTGGCCAA T C PDF,COG8 Ensembl:ENSG00000258429,Ensembl:ENSG00000213380 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1345243633 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9843290,Human_RBP_ID_25245881 35877 RMVar_ID_35877 Human_SNP_ID_607175636 A-to-I Human chr16 - 69328218 69328218 69328218 AAAGTGGCCAGGTGCAGTGGTTCACGCCTGTAATCCCAGCACTTTGGGAGGGCGGGGCGGGTGGA AAAGTGGCCAGGTGCAGTGGTTCACGCCTGTAGTCCCAGCACTTTGGGAGGGCGGGGCGGGTGGA T C PDF,COG8 Ensembl:ENSG00000258429,Ensembl:ENSG00000213380 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1468210799 Functional Loss SNV dbSNP153 33..33 33 - - - 35878 RMVar_ID_35878 Human_SNP_ID_607175642 A-to-I Human chr16 - 69328235 69328235 69328235 CAATGTGTAGGTTTAAGAAAGTGGCCAGGTGCAGTGGTTCACGCCTGTAATCCCAGCACTTTGGG CAATGTGTAGGTTTAAGAAAGTGGCCAGGTGCGGTGGTTCACGCCTGTAATCCCAGCACTTTGGG T C PDF,COG8 Ensembl:ENSG00000258429,Ensembl:ENSG00000213380 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs938103870 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12787695,Human_RBP_ID_26445284 35879 RMVar_ID_35879 Human_SNP_ID_607177273 A-to-I Human chr16 - 69331659 69331659 69331659 GTCTCTACTAAAAATACAAAAATTAGCCTGGCATGGTGGCGGGCGCCTGTAATCCCAGCTACCAC GTCTCTACTAAAAATACAAAAATTAGCCTGGCGTGGTGGCGGGCGCCTGTAATCCCAGCTACCAC T C AC026464.6,COG8 Ensembl:ENSG00000272617,Ensembl:ENSG00000213380 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs527432468 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98220,RMVar_hsa_circ_179396 35880 RMVar_ID_35880 Human_SNP_ID_607181884 A-to-I Human chr16 + 69345815 69345815 69345815 ATTCTACCTAAGCCTCCCGAGTGGCTGGGACCACAAGTATGTGCCACCACACCCGGGTCATTTAA ATTCTACCTAAGCCTCCCGAGTGGCTGGGACCGCAAGTATGTGCCACCACACCCGGGTCATTTAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1567437051 Functional Loss SNV dbSNP153 33..33 33 - - - 35881 RMVar_ID_35881 Human_SNP_ID_607182679 A-to-I Human chr16 + 69348718 69348718 69348718 GCCCACTGCAGTCTCTGCCTCCAGGTTCAAGCAATTCTCTTGCCTCAGCCTCCCAGGTAGCTGGG GCCCACTGCAGTCTCTGCCTCCAGGTTCAAGCGATTCTCTTGCCTCAGCCTCCCAGGTAGCTGGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1009738188 Functional Loss SNV dbSNP153 33..33 33 - - - 35882 RMVar_ID_35882 Human_SNP_ID_607184747 A-to-I Human chr16 - 69356611 69356611 69356611 TATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGGTCTCGATCTCCTGACCTCGTGA TATTTTTAGTAGAGACGGGGTTTCACCGTGTTGGCCAGGATGGTCTCGATCTCCTGACCTCGTGA T C TERF2 Ensembl:ENSG00000132604 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1292447525 Functional Loss SNV dbSNP153 33..33 33 - - - 35883 RMVar_ID_35883 Human_SNP_ID_607185790 A-to-I Human chr16 - 69360521 69360521 69360521 TTTTGTATTTTTAGTAGAGCCAGGGTTTCACCATGTTGGCCAGTATGATCTCGAACTCCTGGGCT TTTTGTATTTTTAGTAGAGCCAGGGTTTCACCGTGTTGGCCAGTATGATCTCGAACTCCTGGGCT T C TERF2 Ensembl:ENSG00000132604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs534613780 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12788263 RMVar_hsa_circ_356783 35884 RMVar_ID_35884 Human_SNP_ID_607190994 A-to-I Human chr16 - 69380594 69380594 69380594 GGAGTATAGTGGCGTGATCTCGGCTTACTGCAAGCTCCGCCTCCTGGGTTCAAGCAGTTCTACAC GGAGTATAGTGGCGTGATCTCGGCTTACTGCAGGCTCCGCCTCCTGGGTTCAAGCAGTTCTACAC T C TERF2 Ensembl:ENSG00000132604 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1487743554 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76940,RMVar_hsa_circ_179404,RMVar_hsa_circ_46401,RMVar_hsa_circ_376738,RMVar_hsa_circ_179408 35885 RMVar_ID_35885 Human_SNP_ID_607204044 A-to-I Human chr16 + 69431726 69431726 69431726 GCCAGGACATCGAGGCTGCAGTGAGCCGAGATAGCACTACTGCACTCCAGCCTGGGTGACAGCGA GCCAGGACATCGAGGCTGCAGTGAGCCGAGATGGCACTACTGCACTCCAGCCTGGGTGACAGCGA A G CYB5B Ensembl:ENSG00000103018 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs552483188 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25245896 35886 RMVar_ID_35886 Human_SNP_ID_607208758 A-to-I Human chr16 + 69452519 69452519 69452519 CCCGGCCAACATGGCGAAACCCCGTTTCTACTAAAAATACAAAAATTAGCTGGGAATGGTGGTGT CCCGGCCAACATGGCGAAACCCCGTTTCTACTCAAAATACAAAAATTAGCTGGGAATGGTGGTGT A C CYB5B Ensembl:ENSG00000103018 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1353615227 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85874,RMVar_hsa_circ_74161,RMVar_hsa_circ_179412,RMVar_hsa_circ_179413 35887 RMVar_ID_35887 Human_SNP_ID_607209369 A-to-I Human chr16 + 69455155 69455155 69455155 TGACCTCATGATCCGCCTGTCTCGGCCTCCCCAAGTGCTGGGATTATAGGCATGAGCCACTGCAC TGACCTCATGATCCGCCTGTCTCGGCCTCCCCCAGTGCTGGGATTATAGGCATGAGCCACTGCAC A C CYB5B Ensembl:ENSG00000103018 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1016835232 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17564255 RMVar_hsa_circ_85874,RMVar_hsa_circ_74161,RMVar_hsa_circ_179412,RMVar_hsa_circ_179413 35888 RMVar_ID_35888 Human_SNP_ID_607238879 A-to-I Human chr16 + 69571183 69571183 69571183 AAAAAAAGCCAGGCATGGTGGCATACACCTGTAATACCAACTACTCGCGATGCTGAGGCAGGAGA AAAAAAAGCCAGGCATGGTGGCATACACCTGTGATACCAACTACTCGCGATGCTGAGGCAGGAGA A G NFAT5 Ensembl:ENSG00000102908 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1332205389 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 35889 RMVar_ID_35889 Human_SNP_ID_607239086 A-to-I Human chr16 + 69571966 69571966 69571966 TGGATTTTTTAGTAGAAACAGGGTTTCACCATATTAGCCAGGATGGTCTCGATCTCCTGATCTCG TGGATTTTTTAGTAGAAACAGGGTTTCACCATGTTAGCCAGGATGGTCTCGATCTCCTGATCTCG A G NFAT5 Ensembl:ENSG00000102908 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs761777490 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 35890 RMVar_ID_35890 Human_SNP_ID_607239764 A-to-I Human chr16 + 69574762 69574762 69574762 ACAATCTTGGCTTATTGCAACCTCTGTCACCCAGGTTCAAGCAATTCTCCCACCAGAGCCTCCCA ACAATCTTGGCTTATTGCAACCTCTGTCACCCGGGTTCAAGCAATTCTCCCACCAGAGCCTCCCA A G NFAT5 Ensembl:ENSG00000102908 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1458139653 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 35891 RMVar_ID_35891 Human_SNP_ID_607240135 A-to-I Human chr16 + 69576185 69576185 69576185 AAATTAGCTGGGCGTGGTGGGCGGGCACCTGTAGTCCCCTGAGGCAGGAGAATGGCTTGAACCCG AAATTAGCTGGGCGTGGTGGGCGGGCACCTGTTGTCCCCTGAGGCAGGAGAATGGCTTGAACCCG A T NFAT5 Ensembl:ENSG00000102908 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs568444978 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12790143,Human_RBP_ID_23697496 RMVar_hsa_circ_86768,RMVar_hsa_circ_350666,RMVar_hsa_circ_90611,RMVar_hsa_circ_179415,RMVar_hsa_circ_179416,RMVar_hsa_circ_179417 35892 RMVar_ID_35892 Human_SNP_ID_607241227 A-to-I Human chr16 + 69580795 69580795 69580795 CTCCGGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGTGCCCGCCACCACGCCTGGCTAATTTTC CTCCGGCCTCAGCCTCCCGAGTAGCTGGGACTGCAGGTGCCCGCCACCACGCCTGGCTAATTTTC A G NFAT5 Ensembl:ENSG00000102908 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1200860333 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 35893 RMVar_ID_35893 Human_SNP_ID_607241351 A-to-I Human chr16 + 69581206 69581206 69581206 GGGACTACAGGAGTGTGCCACCACGCCAGGCTAATTTTTTGTATTTTTAGTAGAGGTGGGGTTTT GGGACTACAGGAGTGTGCCACCACGCCAGGCTCATTTTTTGTATTTTTAGTAGAGGTGGGGTTTT A C NFAT5 Ensembl:ENSG00000102908 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334465119 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 35894 RMVar_ID_35894 Human_SNP_ID_607241352 A-to-I Human chr16 + 69581206 69581206 69581206 GGGACTACAGGAGTGTGCCACCACGCCAGGCTAATTTTTTGTATTTTTAGTAGAGGTGGGGTTTT GGGACTACAGGAGTGTGCCACCACGCCAGGCTGATTTTTTGTATTTTTAGTAGAGGTGGGGTTTT A G NFAT5 Ensembl:ENSG00000102908 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334465119 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 35895 RMVar_ID_35895 Human_SNP_ID_607241361 A-to-I Human chr16 + 69581242 69581242 69581242 TTTTGTATTTTTAGTAGAGGTGGGGTTTTGTTATGTTGGCCAGGGTGGTCTCGAACTCCCGAGTT TTTTGTATTTTTAGTAGAGGTGGGGTTTTGTTGTGTTGGCCAGGGTGGTCTCGAACTCCCGAGTT A G NFAT5 Ensembl:ENSG00000102908 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1182482244 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12790209,Human_RBP_ID_25223492 RMVar_hsa_circ_86768,RMVar_hsa_circ_350666,RMVar_hsa_circ_90611,RMVar_hsa_circ_179415,RMVar_hsa_circ_179416,RMVar_hsa_circ_179417 35896 RMVar_ID_35896 Human_SNP_ID_607242008 A-to-I Human chr16 + 69584115 69584115 69584115 GGGCATGGTGGTGCGCACCTTTAATGCCAGCTACTCGGGAGGTTGAGGCAGGGGAATCGTTTGAA GGGCATGGTGGTGCGCACCTTTAATGCCAGCTCCTCGGGAGGTTGAGGCAGGGGAATCGTTTGAA A C NFAT5 Ensembl:ENSG00000102908 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs367813286 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17565111 RMVar_hsa_circ_86768,RMVar_hsa_circ_350666,RMVar_hsa_circ_90611,RMVar_hsa_circ_179415,RMVar_hsa_circ_179416,RMVar_hsa_circ_179417 35897 RMVar_ID_35897 Human_SNP_ID_607242170 A-to-I Human chr16 + 69584736 69584736 69584736 CCTGAGGCCAGGATGTCGAGGCTGAGTGAGCTATGATTGTACCACTGCACTCCAGTCTGGGTGAC CCTGAGGCCAGGATGTCGAGGCTGAGTGAGCTGTGATTGTACCACTGCACTCCAGTCTGGGTGAC A G NFAT5 Ensembl:ENSG00000102908 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1405576907 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17564261 RMVar_hsa_circ_86768,RMVar_hsa_circ_350666,RMVar_hsa_circ_90611,RMVar_hsa_circ_179415,RMVar_hsa_circ_179416,RMVar_hsa_circ_179417 35898 RMVar_ID_35898 Human_SNP_ID_607243585 A-to-I Human chr16 + 69590053 69590053 69590053 AAAACTAGCCAAGTCTGGTGGCACATGCCTGTAGTCTTAGCTACTTAGGAGACTGATAAAGGAGA AAAACTAGCCAAGTCTGGTGGCACATGCCTGTGGTCTTAGCTACTTAGGAGACTGATAAAGGAGA A G NFAT5 Ensembl:ENSG00000102908 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs757320930 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17564262 RMVar_hsa_circ_86768,RMVar_hsa_circ_350666,RMVar_hsa_circ_90611,RMVar_hsa_circ_179415,RMVar_hsa_circ_179416,RMVar_hsa_circ_179417 35899 RMVar_ID_35899 Human_SNP_ID_607243591 A-to-I Human chr16 + 69590067 69590067 69590067 CTGGTGGCACATGCCTGTAGTCTTAGCTACTTAGGAGACTGATAAAGGAGAATTGCATGACCCCA CTGGTGGCACATGCCTGTAGTCTTAGCTACTTGGGAGACTGATAAAGGAGAATTGCATGACCCCA A G NFAT5 Ensembl:ENSG00000102908 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355133478 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12790352,Human_RBP_ID_17564262 RMVar_hsa_circ_86768,RMVar_hsa_circ_350666,RMVar_hsa_circ_90611,RMVar_hsa_circ_179415,RMVar_hsa_circ_179416,RMVar_hsa_circ_179417 35900 RMVar_ID_35900 Human_SNP_ID_607250229 A-to-I Human chr16 + 69617899 69617899 69617899 CTGTGGAAGGCCGGGCACGGTGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCCAAGGTGGGC CTGTGGAAGGCCGGGCACGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGC A G NFAT5 Ensembl:ENSG00000102908 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1294644122 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17564265 RMVar_hsa_circ_179419,RMVar_hsa_circ_86768,RMVar_hsa_circ_350666,RMVar_hsa_circ_90611,RMVar_hsa_circ_179415,RMVar_hsa_circ_179416,RMVar_hsa_circ_179417,RMVar_hsa_circ_179418 35901 RMVar_ID_35901 Human_SNP_ID_607251369 A-to-I Human chr16 + 69622856 69622856 69622856 TTGTTTGGGAAAAAAAAAAAAAAGAAAAAAATAGACTCGAGGCTGGGTGTGGTGGCTCACGCCTG TTGTTTGGGAAAAAAAAAAAAAAGAAAAAAATCGACTCGAGGCTGGGTGTGGTGGCTCACGCCTG A C NFAT5 Ensembl:ENSG00000102908 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900077037 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_179419,RMVar_hsa_circ_86768,RMVar_hsa_circ_350666,RMVar_hsa_circ_90611,RMVar_hsa_circ_179415,RMVar_hsa_circ_179416,RMVar_hsa_circ_179417,RMVar_hsa_circ_179418 35902 RMVar_ID_35902 Human_SNP_ID_607251413 A-to-I Human chr16 + 69623022 69623022 69623022 ACAAAATTAGCCAGGCATAGTGGTGTATGCCTATAATCTCAGCAACTTGGGAGGCTGAGGCAGGA ACAAAATTAGCCAGGCATAGTGGTGTATGCCTGTAATCTCAGCAACTTGGGAGGCTGAGGCAGGA A G NFAT5 Ensembl:ENSG00000102908 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560527018 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12790660 RMVar_hsa_circ_179419,RMVar_hsa_circ_86768,RMVar_hsa_circ_350666,RMVar_hsa_circ_90611,RMVar_hsa_circ_179415,RMVar_hsa_circ_179416,RMVar_hsa_circ_179417,RMVar_hsa_circ_179418 35903 RMVar_ID_35903 Human_SNP_ID_607253236 A-to-I Human chr16 + 69630146 69630146 69630146 TTTAGTAGAGACGGGGTTTCATTGTGTTGGCCAGGCTGATCTCAAACTCCTGACCTCAGGTGATG TTTAGTAGAGACGGGGTTTCATTGTGTTGGCCTGGCTGATCTCAAACTCCTGACCTCAGGTGATG A T NFAT5 Ensembl:ENSG00000102908 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432588553 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6530471 RMVar_hsa_circ_86768,RMVar_hsa_circ_90611,RMVar_hsa_circ_179416,RMVar_hsa_circ_179417,RMVar_hsa_circ_179421,RMVar_hsa_circ_280353,RMVar_hsa_circ_334411,RMVar_hsa_circ_344469,RMVar_hsa_circ_376693,RMVar_hsa_circ_316767,RMVar_hsa_circ_84295,RMVar_hsa_circ_179420 35904 RMVar_ID_35904 Human_SNP_ID_607253278 A-to-I Human chr16 + 69630292 69630292 69630292 GGGCTCAGGTGATCCTCGAGGCTTGGCCTCCTAAAGTGCTGGGATTACAGGTGTGAACCACTATG GGGCTCAGGTGATCCTCGAGGCTTGGCCTCCTGAAGTGCTGGGATTACAGGTGTGAACCACTATG A G NFAT5 Ensembl:ENSG00000102908 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1448906847 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17690721 RMVar_hsa_circ_86768,RMVar_hsa_circ_90611,RMVar_hsa_circ_179416,RMVar_hsa_circ_179417,RMVar_hsa_circ_179421,RMVar_hsa_circ_280353,RMVar_hsa_circ_334411,RMVar_hsa_circ_344469,RMVar_hsa_circ_376693,RMVar_hsa_circ_316767,RMVar_hsa_circ_84295,RMVar_hsa_circ_179420 35905 RMVar_ID_35905 Human_SNP_ID_607255112 A-to-I Human chr16 + 69638096 69638096 69638096 CAAAAATTATCTGGGCATGGTGGCAGGCACCTATAATTCCAGCTACTCTGGAGTCTGAGGCAGGA CAAAAATTATCTGGGCATGGTGGCAGGCACCTGTAATTCCAGCTACTCTGGAGTCTGAGGCAGGA A G NFAT5 Ensembl:ENSG00000102908 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs573556331 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12790992 RMVar_hsa_circ_86768,RMVar_hsa_circ_90611,RMVar_hsa_circ_179416,RMVar_hsa_circ_179417,RMVar_hsa_circ_179421,RMVar_hsa_circ_280353,RMVar_hsa_circ_334411,RMVar_hsa_circ_344469,RMVar_hsa_circ_376693,RMVar_hsa_circ_316767,RMVar_hsa_circ_84295,RMVar_hsa_circ_179420 35906 RMVar_ID_35906 Human_SNP_ID_607264785 A-to-I Human chr16 + 69679409 69679409 69679409 AGGCCGAGGTGGGCGAATCACTTAAGGCCAGGAATTCAAAACCAGCCTGGCCAACATGGTGAAAC AGGCCGAGGTGGGCGAATCACTTAAGGCCAGGTATTCAAAACCAGCCTGGCCAACATGGTGAAAC A T NFAT5 Ensembl:ENSG00000102908 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1485369415 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86768,RMVar_hsa_circ_179417,RMVar_hsa_circ_316767,RMVar_hsa_circ_84295,RMVar_hsa_circ_179420,RMVar_hsa_circ_332352,RMVar_hsa_circ_327004,RMVar_hsa_circ_179428,RMVar_hsa_circ_45409,RMVar_hsa_circ_300723,RMVar_hsa_circ_179422,RMVar_hsa_circ_343812,RMVar_hsa_circ_351065,RMVar_hsa_circ_266030,RMVar_hsa_circ_179427,RMVar_hsa_circ_16184,RMVar_hsa_circ_271535,RMVar_hsa_circ_47798,RMVar_hsa_circ_71456,RMVar_hsa_circ_321769,RMVar_hsa_circ_179430,RMVar_hsa_circ_179432,RMVar_hsa_circ_100539,RMVar_hsa_circ_312332,RMVar_hsa_circ_179433,RMVar_hsa_circ_179434 35907 RMVar_ID_35907 Human_SNP_ID_607264885 A-to-I Human chr16 + 69679829 69679829 69679829 CATCTAAGGAAATTTGATATAAAATTAATAATAGTTGGCTGGGCATGGTGGCTCACGCCTGTAAT CATCTAAGGAAATTTGATATAAAATTAATAATGGTTGGCTGGGCATGGTGGCTCACGCCTGTAAT A G NFAT5 Ensembl:ENSG00000102908 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1002836142 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6530720 RMVar_hsa_circ_86768,RMVar_hsa_circ_179417,RMVar_hsa_circ_316767,RMVar_hsa_circ_84295,RMVar_hsa_circ_179420,RMVar_hsa_circ_332352,RMVar_hsa_circ_327004,RMVar_hsa_circ_179428,RMVar_hsa_circ_45409,RMVar_hsa_circ_300723,RMVar_hsa_circ_179422,RMVar_hsa_circ_343812,RMVar_hsa_circ_351065,RMVar_hsa_circ_266030,RMVar_hsa_circ_179427,RMVar_hsa_circ_16184,RMVar_hsa_circ_271535,RMVar_hsa_circ_47798,RMVar_hsa_circ_71456,RMVar_hsa_circ_321769,RMVar_hsa_circ_179430,RMVar_hsa_circ_179432,RMVar_hsa_circ_100539,RMVar_hsa_circ_312332,RMVar_hsa_circ_179433,RMVar_hsa_circ_179434 35908 RMVar_ID_35908 Human_SNP_ID_607266866 A-to-I Human chr16 + 69687279 69687279 69687279 CCTGGCCAACATGGCAAAACCCTGTCTCTACTAAAAATAAAAAAATTAGCTGGGCGTGGTGGTGT CCTGGCCAACATGGCAAAACCCTGTCTCTACTGAAAATAAAAAAATTAGCTGGGCGTGGTGGTGT A G NFAT5 Ensembl:ENSG00000102908 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1142100 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86768,RMVar_hsa_circ_179417,RMVar_hsa_circ_84295,RMVar_hsa_circ_179420,RMVar_hsa_circ_327004,RMVar_hsa_circ_179428,RMVar_hsa_circ_45409,RMVar_hsa_circ_300723,RMVar_hsa_circ_179422,RMVar_hsa_circ_343812,RMVar_hsa_circ_266030,RMVar_hsa_circ_16184,RMVar_hsa_circ_321769,RMVar_hsa_circ_58552,RMVar_hsa_circ_179434,RMVar_hsa_circ_56384,RMVar_hsa_circ_325814,RMVar_hsa_circ_351878 35909 RMVar_ID_35909 Human_SNP_ID_607267521 A-to-I Human chr16 + 69689613 69689613 69689613 TTGCCCAGCCTGCAGTACAGTAGAGCGATCTCAGCTCATTGCAACCACCTCCTCCTGGATTCAAG TTGCCCAGCCTGCAGTACAGTAGAGCGATCTCGGCTCATTGCAACCACCTCCTCCTGGATTCAAG A G NFAT5 Ensembl:ENSG00000102908 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1034438352 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86768,RMVar_hsa_circ_179417,RMVar_hsa_circ_84295,RMVar_hsa_circ_179420,RMVar_hsa_circ_327004,RMVar_hsa_circ_179428,RMVar_hsa_circ_45409,RMVar_hsa_circ_300723,RMVar_hsa_circ_179422,RMVar_hsa_circ_343812,RMVar_hsa_circ_266030,RMVar_hsa_circ_16184,RMVar_hsa_circ_321769,RMVar_hsa_circ_58552,RMVar_hsa_circ_179434,RMVar_hsa_circ_56384,RMVar_hsa_circ_325814,RMVar_hsa_circ_351878 35910 RMVar_ID_35910 Human_SNP_ID_607267543 A-to-I Human chr16 + 69689710 69689710 69689710 GGATTTACAGGCATGTGCCACCATGCCCTGCTAATTTTTGTATTTTTAGTAGAGACAGAGTTTCA GGATTTACAGGCATGTGCCACCATGCCCTGCTTATTTTTGTATTTTTAGTAGAGACAGAGTTTCA A T NFAT5 Ensembl:ENSG00000102908 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs945557375 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86768,RMVar_hsa_circ_179417,RMVar_hsa_circ_84295,RMVar_hsa_circ_179420,RMVar_hsa_circ_327004,RMVar_hsa_circ_179428,RMVar_hsa_circ_45409,RMVar_hsa_circ_300723,RMVar_hsa_circ_179422,RMVar_hsa_circ_343812,RMVar_hsa_circ_266030,RMVar_hsa_circ_16184,RMVar_hsa_circ_321769,RMVar_hsa_circ_58552,RMVar_hsa_circ_179434,RMVar_hsa_circ_56384,RMVar_hsa_circ_325814,RMVar_hsa_circ_351878 35911 RMVar_ID_35911 Human_SNP_ID_607272780 A-to-I Human chr16 - 69712786 69712786 69712786 TAGCCAGGCTGGTTTCAAACACTTGACCTCAAATGATTCTCCTGCCTCAGCCTCCCAAAGTGCTG TAGCCAGGCTGGTTTCAAACACTTGACCTCAAGTGATTCTCCTGCCTCAGCCTCCCAAAGTGCTG T C NQO1 Ensembl:ENSG00000181019 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs771494456 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29782,RMVar_hsa_circ_41946 35912 RMVar_ID_35912 Human_SNP_ID_607273599 A-to-I Human chr16 - 69715652 69715652 69715652 GTGATTCTCCTGCCTCAACAGCCCGAGTAGCTAGGACTACAGGCGTGCGCCACCACGCCCGGTTG GTGATTCTCCTGCCTCAACAGCCCGAGTAGCTCGGACTACAGGCGTGCGCCACCACGCCCGGTTG T G NQO1 Ensembl:ENSG00000181019 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1394343659 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41946,RMVar_hsa_circ_333431,RMVar_hsa_circ_110172,RMVar_hsa_circ_179438,RMVar_hsa_circ_179439,RMVar_hsa_circ_179440,RMVar_hsa_circ_330725 35913 RMVar_ID_35913 Human_SNP_ID_607277086 A-to-I Human chr16 + 69728999 69728999 69728999 TTCACTGCAGCCTCGACCTTCTGGAGTCAAGCAATCCTCCTGCCCCAGCCTCCTGAGTAGCTGAG TTCACTGCAGCCTCGACCTTCTGGAGTCAAGCGATCCTCCTGCCCCAGCCTCCTGAGTAGCTGAG A G AC092115.4 Ensembl:ENSG00000262136 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1227835509 Functional Loss SNV dbSNP153 33..33 33 - - - 35914 RMVar_ID_35914 Human_SNP_ID_607278430 A-to-I Human chr16 - 69733846 69733846 69733846 GGCATGCGCCACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATCTGGG GGCATGCGCCACCACGCCCAGCTAATTTTTGTGTTTTTAGTAGAGACGGGGTTTCACCATCTGGG T C L13304-001 RNACentral:URS000044B5AA scRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs896627684 Functional Loss SNV dbSNP153 33..33 33 - - - 35915 RMVar_ID_35915 Human_SNP_ID_607278690 A-to-I Human chr16 - 69734568 69734568 69734568 AAATTAGCTGGGCATGATGATGGGCACCTGTAATCCCAGCTTCTTGGGAGGCTGAGGCAGGAGAA AAATTAGCTGGGCATGATGATGGGCACCTGTATTCCCAGCTTCTTGGGAGGCTGAGGCAGGAGAA T A L13304-001 RNACentral:URS000044B5AA scRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459678768 Functional Loss SNV dbSNP153 33..33 33 - - - 35916 RMVar_ID_35916 Human_SNP_ID_607279308 A-to-I Human chr16 - 69736685 69736685 69736685 ACCCAGATAATTTCTGTAGTTTTAGTAGAGACAGGTTTCACCATGTTGGCCAGGCTGGTTTCAAA ACCCAGATAATTTCTGTAGTTTTAGTAGAGACGGGTTTCACCATGTTGGCCAGGCTGGTTTCAAA T C L13304-001 RNACentral:URS000044B5AA scRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs550927160 Functional Loss SNV dbSNP153 33..33 33 - - - 35917 RMVar_ID_35917 Human_SNP_ID_607279310 A-to-I Human chr16 - 69736694 69736694 69736694 TACCACTACACCCAGATAATTTCTGTAGTTTTAGTAGAGACAGGTTTCACCATGTTGGCCAGGCT TACCACTACACCCAGATAATTTCTGTAGTTTTCGTAGAGACAGGTTTCACCATGTTGGCCAGGCT T G L13304-001 RNACentral:URS000044B5AA scRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1330365393 Functional Loss SNV dbSNP153 33..33 33 - - - 35918 RMVar_ID_35918 Human_SNP_ID_607283729 A-to-I Human chr16 - 69750187 69750187 69750187 CAGCCTGGCCAACATGGCGAAACCCCATCTCTACTAAAAAATACAAAAATCAGTGGGGCATGGTG CAGCCTGGCCAACATGGCGAAACCCCATCTCTTCTAAAAAATACAAAAATCAGTGGGGCATGGTG T A NOB1 Ensembl:ENSG00000141101 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1488128730 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2947,RMVar_hsa_circ_107685,RMVar_hsa_circ_112970,RMVar_hsa_circ_179442,RMVar_hsa_circ_179443,RMVar_hsa_circ_34455 35919 RMVar_ID_35919 Human_SNP_ID_607283734 A-to-I Human chr16 - 69750206 69750206 69750206 GAGGCTGGGAGTTTGAGACCAGCCTGGCCAACATGGCGAAACCCCATCTCTACTAAAAAATACAA GAGGCTGGGAGTTTGAGACCAGCCTGGCCAACGTGGCGAAACCCCATCTCTACTAAAAAATACAA T C NOB1 Ensembl:ENSG00000141101 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1310928655 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2947,RMVar_hsa_circ_107685,RMVar_hsa_circ_112970,RMVar_hsa_circ_179442,RMVar_hsa_circ_179443,RMVar_hsa_circ_34455 35920 RMVar_ID_35920 Human_SNP_ID_607285694 A-to-I Human chr16 - 69757008 69757008 69757008 GCCATAAGCACCAGGTCATGCTAATGAGACAGAATTTGATGAGGCGCCAAGAAGAACTTCGGAGG GCCATAAGCACCAGGTCATGCTAATGAGACAGGATTTGATGAGGCGCCAAGAAGAACTTCGGAGG T C AC092115.2 Ensembl:ENSG00000260290 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879153615 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3510790,Human_RBP_ID_5096630,Human_RBP_ID_5274706,Human_RBP_ID_5573259,Human_RBP_ID_6550171,Human_RBP_ID_8252433,Human_RBP_ID_9257151,Human_RBP_ID_17488826,Human_RBP_ID_18513297,Human_RBP_ID_18530310,Human_RBP_ID_26446959 35921 RMVar_ID_35921 Human_SNP_ID_607285702 A-to-I Human chr16 - 69757035 69757035 69757035 AGCCAGAGATGGAGATGGAGGCTGCACGCCATAAGCACCAGGTCATGCTAATGAGACAGAATTTG AGCCAGAGATGGAGATGGAGGCTGCACGCCATGAGCACCAGGTCATGCTAATGAGACAGAATTTG T C AC092115.2 Ensembl:ENSG00000260290 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879127181 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5573259 35922 RMVar_ID_35922 Human_SNP_ID_607287685 A-to-I Human chr16 + 69764279 69764279 69764279 TGGAGTGCAGTGGCACAATCACGGCTCACTGTAACCTTGACCTGCCTGGGCTCGGGTGATCCTCC TGGAGTGCAGTGGCACAATCACGGCTCACTGTGACCTTGACCTGCCTGGGCTCGGGTGATCCTCC A G WWP2 Ensembl:ENSG00000198373 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs914126026 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104988,RMVar_hsa_circ_179448 35923 RMVar_ID_35923 Human_SNP_ID_607289983 A-to-I Human chr16 + 69774330 69774330 69774330 CTAGCTGGAGTGCAGTGGCGTGATCATAGCTCACTGCAGCCTAGACCTCCCAGGCTCAAGCGATC CTAGCTGGAGTGCAGTGGCGTGATCATAGCTCGCTGCAGCCTAGACCTCCCAGGCTCAAGCGATC A G WWP2 Ensembl:ENSG00000198373 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs966155544 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104988,RMVar_hsa_circ_179448 35924 RMVar_ID_35924 Human_SNP_ID_607293512 A-to-I Human chr16 + 69787479 69787479 69787479 GGCATAGTGGTGCATGCTAGCTGGTCCCAGCTACTAAGGACACTGAAGTGGGAGGATCGCTTGAG GGCATAGTGGTGCATGCTAGCTGGTCCCAGCTTCTAAGGACACTGAAGTGGGAGGATCGCTTGAG A T WWP2 Ensembl:ENSG00000198373 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1337464000 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14205,RMVar_hsa_circ_104988,RMVar_hsa_circ_179448,RMVar_hsa_circ_323660,RMVar_hsa_circ_374447,RMVar_hsa_circ_292245,RMVar_hsa_circ_179453,RMVar_hsa_circ_84431,RMVar_hsa_circ_179450,RMVar_hsa_circ_179451,RMVar_hsa_circ_371674,RMVar_hsa_circ_31916,RMVar_hsa_circ_293820,RMVar_hsa_circ_32641,RMVar_hsa_circ_179454,RMVar_hsa_circ_179452 35925 RMVar_ID_35925 Human_SNP_ID_607294802 A-to-I Human chr16 + 69792769 69792769 69792769 GCTAGAGTGCAGTGGCACAATTACAGCTCACTACAGCCTCGACCTCCTGGGCTCCAGGGATCCTC GCTAGAGTGCAGTGGCACAATTACAGCTCACTGCAGCCTCGACCTCCTGGGCTCCAGGGATCCTC A G WWP2 Ensembl:ENSG00000198373 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs952103843 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14205,RMVar_hsa_circ_104988,RMVar_hsa_circ_179448,RMVar_hsa_circ_323660,RMVar_hsa_circ_374447,RMVar_hsa_circ_292245,RMVar_hsa_circ_179453,RMVar_hsa_circ_84431,RMVar_hsa_circ_179450,RMVar_hsa_circ_179451,RMVar_hsa_circ_371674,RMVar_hsa_circ_31916,RMVar_hsa_circ_293820,RMVar_hsa_circ_32641,RMVar_hsa_circ_179454,RMVar_hsa_circ_179452 35926 RMVar_ID_35926 Human_SNP_ID_607300546 A-to-I Human chr16 + 69814260 69814260 69814260 ATAGGTAACTGTAGCCTCGAACTCCTGGGCTCAAGCGATCCTCTTGCCTCAGCCTCCAGAGTTGC ATAGGTAACTGTAGCCTCGAACTCCTGGGCTCGAGCGATCCTCTTGCCTCAGCCTCCAGAGTTGC A G WWP2 Ensembl:ENSG00000198373 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs541558737 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14205,RMVar_hsa_circ_104988,RMVar_hsa_circ_179448,RMVar_hsa_circ_323660,RMVar_hsa_circ_374447,RMVar_hsa_circ_179451,RMVar_hsa_circ_371674,RMVar_hsa_circ_32641,RMVar_hsa_circ_120734,RMVar_hsa_circ_179452,RMVar_hsa_circ_179456 35927 RMVar_ID_35927 Human_SNP_ID_607304135 A-to-I Human chr16 + 69827343 69827343 69827343 GCATTCTATAATGTCAGAGGTTGCAGTGAGCCAAGATCGCGCCACTGCACTCCAGCCTGGGCGAC GCATTCTATAATGTCAGAGGTTGCAGTGAGCCGAGATCGCGCCACTGCACTCCAGCCTGGGCGAC A G WWP2 Ensembl:ENSG00000198373 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1374891560 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14205,RMVar_hsa_circ_104988,RMVar_hsa_circ_179448,RMVar_hsa_circ_323660,RMVar_hsa_circ_374447,RMVar_hsa_circ_179451,RMVar_hsa_circ_371674,RMVar_hsa_circ_32641,RMVar_hsa_circ_120734,RMVar_hsa_circ_179452,RMVar_hsa_circ_179456 35928 RMVar_ID_35928 Human_SNP_ID_607326375 A-to-I Human chr16 + 69916298 69916298 69916298 TTCACTGTAGCCTTGATCTCCCAGGCACAAGCAGTCCTCCCACCTCAGCTGCCCAAGTAGCTGGG TTCACTGTAGCCTTGATCTCCCAGGCACAAGCTGTCCTCCCACCTCAGCTGCCCAAGTAGCTGGG A T WWP2 Ensembl:ENSG00000198373 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924308236 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3147,RMVar_hsa_circ_104988,RMVar_hsa_circ_179448,RMVar_hsa_circ_122846,RMVar_hsa_circ_179459,RMVar_hsa_circ_84734,RMVar_hsa_circ_268531,RMVar_hsa_circ_179461,RMVar_hsa_circ_360520,RMVar_hsa_circ_373654,RMVar_hsa_circ_179463 35929 RMVar_ID_35929 Human_SNP_ID_607337073 A-to-I Human chr16 + 69955990 69955990 69955990 ACACAAGGCTGGGTGCGGTGGCTCACGCCCGTAATCCCAGCACTTTGGGAGGCCAAGGTGGCAGG ACACAAGGCTGGGTGCGGTGGCTCACGCCCGTGATCCCAGCACTTTGGGAGGCCAAGGTGGCAGG A G CLEC18A Ensembl:ENSG00000157322 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1454016551 Functional Loss SNV dbSNP153 33..33 33 - - - 35930 RMVar_ID_35930 Human_SNP_ID_607356060 A-to-I Human chr16 - 70026649 70026649 70026649 CCCAGCTACTTAGGAGGCCGAGGCGGGAGAATAGCTTGAATCCAGGAGGCTGAGATTGCAGTGAG CCCAGCTACTTAGGAGGCCGAGGCGGGAGAATCGCTTGAATCCAGGAGGCTGAGATTGCAGTGAG T G PDXDC2P,AC009022.1 Ensembl:ENSG00000255185,Ensembl:ENSG00000196696 Pseudogene,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1039215252 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266162,RMVar_hsa_circ_115035,RMVar_hsa_circ_179473,RMVar_hsa_circ_91912,RMVar_hsa_circ_365657,RMVar_hsa_circ_51635,RMVar_hsa_circ_89979,RMVar_hsa_circ_179479,RMVar_hsa_circ_179480,RMVar_hsa_circ_179484,RMVar_hsa_circ_269489,RMVar_hsa_circ_304761,RMVar_hsa_circ_24750,RMVar_hsa_circ_65977,RMVar_hsa_circ_179487,RMVar_hsa_circ_312875,RMVar_hsa_circ_276689,RMVar_hsa_circ_326571,RMVar_hsa_circ_179488 35931 RMVar_ID_35931 Human_SNP_ID_607366258 A-to-I Human chr16 + 70063521 70063521 70063521 TGAGACCATCCTGACCAACATGGTGAAACCCCATCTCTACTGGGAATACAAAAATTAGTCGGGTG TGAGACCATCCTGACCAACATGGTGAAACCCCGTCTCTACTGGGAATACAAAAATTAGTCGGGTG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1435622138 Functional Loss SNV dbSNP153 33..33 33 - - - 35932 RMVar_ID_35932 Human_SNP_ID_607380099 A-to-I Human chr16 + 70116163 70116163 70116163 GCAGTGGCGCGAATCTGCCCACTGCAGCCTCCATCTCCCTGGTTGAAGCAATTTTCCTGTCTCAG GCAGTGGCGCGAATCTGCCCACTGCAGCCTCCCTCTCCCTGGTTGAAGCAATTTTCCTGTCTCAG A C PDPR Ensembl:ENSG00000090857 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1286136554 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23697881 RMVar_hsa_circ_179493,RMVar_hsa_circ_91980,RMVar_hsa_circ_100604,RMVar_hsa_circ_179494 35933 RMVar_ID_35933 Human_SNP_ID_607380100 A-to-I Human chr16 + 70116163 70116163 70116163 GCAGTGGCGCGAATCTGCCCACTGCAGCCTCCATCTCCCTGGTTGAAGCAATTTTCCTGTCTCAG GCAGTGGCGCGAATCTGCCCACTGCAGCCTCCGTCTCCCTGGTTGAAGCAATTTTCCTGTCTCAG A G PDPR Ensembl:ENSG00000090857 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1286136554 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23697881 RMVar_hsa_circ_179493,RMVar_hsa_circ_91980,RMVar_hsa_circ_100604,RMVar_hsa_circ_179494 35934 RMVar_ID_35934 Human_SNP_ID_607380598 A-to-I Human chr16 + 70117972 70117972 70117972 AAAAGTAACTGGGCGTGGTGGCGCGTGCTTGTAGTTCCAGCTGTTCAGGAGGCCGAGGCAGGAGA AAAAGTAACTGGGCGTGGTGGCGCGTGCTTGTTGTTCCAGCTGTTCAGGAGGCCGAGGCAGGAGA A T PDPR Ensembl:ENSG00000090857 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1253788958 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_815991,Human_RBP_ID_12793915 RMVar_hsa_circ_179493,RMVar_hsa_circ_91980,RMVar_hsa_circ_100604,RMVar_hsa_circ_179494 35935 RMVar_ID_35935 Human_SNP_ID_607380957 A-to-I Human chr16 + 70119205 70119205 70119205 TGCCTTGTCCAAGGGCAGTGGTTCATGCCTGTAATCTCAACACTTTGGGAGACCAAGGTGGGAGG TGCCTTGTCCAAGGGCAGTGGTTCATGCCTGTTATCTCAACACTTTGGGAGACCAAGGTGGGAGG A T PDPR Ensembl:ENSG00000090857 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs970279899 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_179493,RMVar_hsa_circ_91980,RMVar_hsa_circ_100604,RMVar_hsa_circ_179494 35936 RMVar_ID_35936 Human_SNP_ID_607381217 A-to-I Human chr16 + 70120016 70120016 70120016 TCTGCTCGCTGCAGCCTCCGCCTCCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGC TCTGCTCGCTGCAGCCTCCGCCTCCCGGGTTCCAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGC A C PDPR Ensembl:ENSG00000090857 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1480590754 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_179493,RMVar_hsa_circ_91980,RMVar_hsa_circ_100604,RMVar_hsa_circ_179494 35937 RMVar_ID_35937 Human_SNP_ID_607381219 A-to-I Human chr16 + 70120020 70120020 70120020 CTCGCTGCAGCCTCCGCCTCCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGG CTCGCTGCAGCCTCCGCCTCCCGGGTTCAAGCCATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGG A C PDPR Ensembl:ENSG00000090857 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1171259980 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_179493,RMVar_hsa_circ_91980,RMVar_hsa_circ_100604,RMVar_hsa_circ_179494 35938 RMVar_ID_35938 Human_SNP_ID_607381261 A-to-I Human chr16 + 70120176 70120176 70120176 TGACCTCGTTATCCACTCGCCGCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACTGCGC TGACCTCGTTATCCACTCGCCGCGGCCTCCCACAGTGCTGGGATTACAGGTGTGAGCCACTGCGC A C PDPR Ensembl:ENSG00000090857 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs139936903 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_179493,RMVar_hsa_circ_91980,RMVar_hsa_circ_100604,RMVar_hsa_circ_179494 35939 RMVar_ID_35939 Human_SNP_ID_607381262 A-to-I Human chr16 + 70120176 70120176 70120176 TGACCTCGTTATCCACTCGCCGCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACTGCGC TGACCTCGTTATCCACTCGCCGCGGCCTCCCAGAGTGCTGGGATTACAGGTGTGAGCCACTGCGC A G PDPR Ensembl:ENSG00000090857 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs139936903 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_179493,RMVar_hsa_circ_91980,RMVar_hsa_circ_100604,RMVar_hsa_circ_179494 35940 RMVar_ID_35940 Human_SNP_ID_607381263 A-to-I Human chr16 + 70120176 70120176 70120176 TGACCTCGTTATCCACTCGCCGCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACTGCGC TGACCTCGTTATCCACTCGCCGCGGCCTCCCATAGTGCTGGGATTACAGGTGTGAGCCACTGCGC A T PDPR Ensembl:ENSG00000090857 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs139936903 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_179493,RMVar_hsa_circ_91980,RMVar_hsa_circ_100604,RMVar_hsa_circ_179494 35941 RMVar_ID_35941 Human_SNP_ID_607381921 A-to-I Human chr16 + 70121890 70121889 70121890 GGATTCAAGCAGTCCTTCTGCCATAGCCTTCCAAGTAGCTGGGACTACTGACATGCACCACCACA GGATTCAAGCAGTCCTTCTGCCATAGCCTTCC_AGTAGCTGGGACTACTGACATGCACCACCACA CA C PDPR Ensembl:ENSG00000090857 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1468780253 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_29876,RMVar_hsa_circ_179493,RMVar_hsa_circ_91980,RMVar_hsa_circ_100604,RMVar_hsa_circ_179494,RMVar_hsa_circ_342526,RMVar_hsa_circ_348908,RMVar_hsa_circ_366247,RMVar_hsa_circ_313549,RMVar_hsa_circ_288574,RMVar_hsa_circ_298950,RMVar_hsa_circ_125317,RMVar_hsa_circ_28534,RMVar_hsa_circ_179496 35942 RMVar_ID_35942 Human_SNP_ID_607387969 A-to-I Human chr16 + 70137169 70137169 70137169 GGTCATGAGATCGAGACCACTCTGGCTAACACAGTGAAACCCCATCTCTACTAAAAATACACAAA GGTCATGAGATCGAGACCACTCTGGCTAACACGGTGAAACCCCATCTCTACTAAAAATACACAAA A G PDPR Ensembl:ENSG00000090857 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs543742528 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78706,RMVar_hsa_circ_100604,RMVar_hsa_circ_179494,RMVar_hsa_circ_366247,RMVar_hsa_circ_313549,RMVar_hsa_circ_298950,RMVar_hsa_circ_125317,RMVar_hsa_circ_28534,RMVar_hsa_circ_179496,RMVar_hsa_circ_326014,RMVar_hsa_circ_298121,RMVar_hsa_circ_108198,RMVar_hsa_circ_75535,RMVar_hsa_circ_179497,RMVar_hsa_circ_179498,RMVar_hsa_circ_179500,RMVar_hsa_circ_107696,RMVar_hsa_circ_111185,RMVar_hsa_circ_179501,RMVar_hsa_circ_89384,RMVar_hsa_circ_82138,RMVar_hsa_circ_127643,RMVar_hsa_circ_179503,RMVar_hsa_circ_179504,RMVar_hsa_circ_179505,RMVar_hsa_circ_111461,RMVar_hsa_circ_179507,RMVar_hsa_circ_85466,RMVar_hsa_circ_179506,RMVar_hsa_circ_101950,RMVar_hsa_circ_179508,RMVar_hsa_circ_179509,RMVar_hsa_circ_179510 35943 RMVar_ID_35943 Human_SNP_ID_607394494 A-to-I Human chr16 + 70155008 70155008 70155008 GAGTTCACAAGTTCGAGACCAGCCCGGCCAACATGGTGAAACCCCGTATCTGCTAAAAATATAAA GAGTTCACAAGTTCGAGACCAGCCCGGCCAACGTGGTGAAACCCCGTATCTGCTAAAAATATAAA A G PDPR Ensembl:ENSG00000090857 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1269450141 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_179523,RMVar_hsa_circ_76174 35944 RMVar_ID_35944 Human_SNP_ID_607394495 A-to-I Human chr16 + 70155008 70155008 70155008 GAGTTCACAAGTTCGAGACCAGCCCGGCCAACATGGTGAAACCCCGTATCTGCTAAAAATATAAA GAGTTCACAAGTTCGAGACCAGCCCGGCCAACTTGGTGAAACCCCGTATCTGCTAAAAATATAAA A T PDPR Ensembl:ENSG00000090857 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1269450141 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_179523,RMVar_hsa_circ_76174 35945 RMVar_ID_35945 Human_SNP_ID_607398064 A-to-I Human chr16 + 70164732 70164732 70164732 AAATACAAAATTAGGCGTGGTAGCGCATGCCTATAATCCCAGCTTCGCGGGAGGCTGAGGCAGGA AAATACAAAATTAGGCGTGGTAGCGCATGCCTGTAATCCCAGCTTCGCGGGAGGCTGAGGCAGGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1288097894 Functional Loss SNV dbSNP153 33..33 33 - - - 35946 RMVar_ID_35946 Human_SNP_ID_607401853 A-to-I Human chr16 + 70178402 70178402 70178402 CCTCAGCCTCCCAAGTAGCTAGGACTACAGGCACGAGCCACCACACCCCACTAATTTTTGTATTT CCTCAGCCTCCCAAGTAGCTAGGACTACAGGCGCGAGCCACCACACCCCACTAATTTTTGTATTT A G CLEC18C Ensembl:ENSG00000157335 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1477040455 Functional Loss SNV dbSNP153 33..33 33 - - - 35947 RMVar_ID_35947 Human_SNP_ID_607410162 A-to-I Human chr16 - 70207867 70207867 70207867 AGGAGGAGGGGCACGGGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGGGGCCGAGACAGGTGG AGGAGGAGGGGCACGGGGTGGCTCACGCCTGTGATCCCAGCACTTTGGGGGGCCGAGACAGGTGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1452653331 Functional Loss SNV dbSNP153 33..33 33 - - - 35948 RMVar_ID_35948 Human_SNP_ID_607410486 A-to-I Human chr16 - 70208985 70208985 70208985 GTGATCTCAGCTCACTGTAACCTCAACCTCCCAGGCTCAAGCAGTCCTCTCACTTCAGCCTCCCA GTGATCTCAGCTCACTGTAACCTCAACCTCCCGGGCTCAAGCAGTCCTCTCACTTCAGCCTCCCA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs930029658 Functional Loss SNV dbSNP153 33..33 33 - - - 35949 RMVar_ID_35949 Human_SNP_ID_607418385 A-to-I Human chr16 - 70240789 70240789 70240789 AGCTTGGTGTAGTGGTGTGCACCTGCAGTCCTAGCTACTCGGGAGGCTGAGGGAGGAGGATCGAT AGCTTGGTGTAGTGGTGTGCACCTGCAGTCCTGGCTACTCGGGAGGCTGAGGGAGGAGGATCGAT T C SMG1P7 Ensembl:ENSG00000261556 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1213284712 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_361547 35950 RMVar_ID_35950 Human_SNP_ID_607420036 A-to-I Human chr16 - 70247992 70247992 70247992 GGAGGGCAGTGGCACAATCTCGGCTCACTGCAACCTCCGCCTCCCAGGTTCAAGCAGTTCTCATG GGAGGGCAGTGGCACAATCTCGGCTCACTGCAGCCTCCGCCTCCCAGGTTCAAGCAGTTCTCATG T C EXOSC6 Ensembl:ENSG00000223496 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1249331690 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8185948,Human_RBP_ID_12794499 35951 RMVar_ID_35951 Human_SNP_ID_607420037 A-to-I Human chr16 - 70247992 70247992 70247992 GGAGGGCAGTGGCACAATCTCGGCTCACTGCAACCTCCGCCTCCCAGGTTCAAGCAGTTCTCATG GGAGGGCAGTGGCACAATCTCGGCTCACTGCACCCTCCGCCTCCCAGGTTCAAGCAGTTCTCATG T G EXOSC6 Ensembl:ENSG00000223496 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1249331690 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8185948,Human_RBP_ID_12794499 35952 RMVar_ID_35952 Human_SNP_ID_607420229 A-to-I Human chr16 - 70248674 70248674 70248674 GGAGGATCGCTTGTGCCTGGGAGGTTGAAGCTACAGTGAGCTATGGTCAAGCTACTGCACTCCAT GGAGGATCGCTTGTGCCTGGGAGGTTGAAGCTGCAGTGAGCTATGGTCAAGCTACTGCACTCCAT T C EXOSC6 Ensembl:ENSG00000223496 Protein coding 3'UTR GSE38233;GSE112787;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;293 Flip-In T-REx cells,empty vector;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29967493,31158229,31158229 RNA-Seq:(High) rs891808617 Functional Loss SNV dbSNP153 33..33 33 - - - 35953 RMVar_ID_35953 Human_SNP_ID_607420327 A-to-I Human chr16 - 70248848 70248848 70248848 ACTGTGGGAGGCTGAGGCTGGTGAATCGCCTGAGTCCAGGAGTTTGAGACCAGCCTGGGCAACAA ACTGTGGGAGGCTGAGGCTGGTGAATCGCCTGGGTCCAGGAGTTTGAGACCAGCCTGGGCAACAA T C EXOSC6 Ensembl:ENSG00000223496 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs953940007 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26445313 35954 RMVar_ID_35954 Human_SNP_ID_607420711 A-to-I Human chr16 - 70249877 70249877 70249877 GCGCGATCTCAGCTCACTGCAACCTCCGCCTCAGAGGTTCAAGTGATTCTCCTGCCTCAGCCTCT GCGCGATCTCAGCTCACTGCAACCTCCGCCTCGGAGGTTCAAGTGATTCTCCTGCCTCAGCCTCT T C EXOSC6 Ensembl:ENSG00000223496 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs1365566940 Functional Loss SNV dbSNP153 33..33 33 - - - 35955 RMVar_ID_35955 Human_SNP_ID_607420717 A-to-I Human chr16 - 70249889 70249889 70249889 TGGAGTGCAATGGCGCGATCTCAGCTCACTGCAACCTCCGCCTCAGAGGTTCAAGTGATTCTCCT TGGAGTGCAATGGCGCGATCTCAGCTCACTGCCACCTCCGCCTCAGAGGTTCAAGTGATTCTCCT T G EXOSC6 Ensembl:ENSG00000223496 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1290371384 Functional Loss SNV dbSNP153 33..33 33 - - - 35956 RMVar_ID_35956 Human_SNP_ID_607420730 A-to-I Human chr16 - 70249912 70249912 70249912 GAGTCTCACTCTGTTGCCCAGGCTGGAGTGCAATGGCGCGATCTCAGCTCACTGCAACCTCCGCC GAGTCTCACTCTGTTGCCCAGGCTGGAGTGCAGTGGCGCGATCTCAGCTCACTGCAACCTCCGCC T C EXOSC6 Ensembl:ENSG00000223496 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,31158229,31158229 RNA-Seq:(High) rs766126476 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1075392 35957 RMVar_ID_35957 Human_SNP_ID_607420909 A-to-I Human chr16 - 70250424 70250424 70250424 CCTCAGGTGATCCACCCGCCTTGGCCTCCCAAAGTGCTGGAATTACAGGTGTGAGCCACTGTGCC CCTCAGGTGATCCACCCGCCTTGGCCTCCCAAGGTGCTGGAATTACAGGTGTGAGCCACTGTGCC T C EXOSC6 Ensembl:ENSG00000223496 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1405951945 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4380622,Human_RBP_ID_25224777 35958 RMVar_ID_35958 Human_SNP_ID_607423449 A-to-I Human chr16 - 70256372 70256360 70256373 TGAAACTGGGAGGCAGAGGTTGTGGTGAGCCAAGATCACACCATTGCACTCCAGCCTGAACAACA TGAAACTGGGAGGCAGAGGTTGTGGTGAGCC_____________TGCACTCCAGCCTGAACAACA AATGGTGTGATCTT A AARS1 Ensembl:ENSG00000090861 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1279071588 Functional Loss DEL dbSNP153 32..44 33 - - - 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_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_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_46263,RMVar_hsa_circ_179553,RMVar_hsa_circ_179554,RMVar_hsa_circ_290304,RMVar_hsa_circ_325291,RMVar_hsa_circ_179552,RMVar_hsa_circ_321816,RMVar_hsa_circ_284628,RMVar_hsa_circ_179556,RMVar_hsa_circ_179557,RMVar_hsa_circ_179555 35959 RMVar_ID_35959 Human_SNP_ID_607423449 A-to-I Human chr16 - 70256373 70256360 70256373 TTGAAACTGGGAGGCAGAGGTTGTGGTGAGCCAAGATCACACCATTGCACTCCAGCCTGAACAAC TTGAAACTGGGAGGCAGAGGTTGTGGTGAGCC_____________TGCACTCCAGCCTGAACAAC AATGGTGTGATCTT A AARS1 Ensembl:ENSG00000090861 Protein coding intron GSE38233;GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,32596459 RNA-Seq:(High) rs1279071588 Functional Loss DEL dbSNP153 33..45 33 - - - 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_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_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_46263,RMVar_hsa_circ_179553,RMVar_hsa_circ_179554,RMVar_hsa_circ_290304,RMVar_hsa_circ_325291,RMVar_hsa_circ_179552,RMVar_hsa_circ_321816,RMVar_hsa_circ_284628,RMVar_hsa_circ_179556,RMVar_hsa_circ_179557,RMVar_hsa_circ_179555 35960 RMVar_ID_35960 Human_SNP_ID_607423451 A-to-I Human chr16 - 70256372 70256372 70256372 TGAAACTGGGAGGCAGAGGTTGTGGTGAGCCAAGATCACACCATTGCACTCCAGCCTGAACAACA TGAAACTGGGAGGCAGAGGTTGTGGTGAGCCAGGATCACACCATTGCACTCCAGCCTGAACAACA T C AARS1 Ensembl:ENSG00000090861 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1040171296 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_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_46263,RMVar_hsa_circ_179553,RMVar_hsa_circ_179554,RMVar_hsa_circ_290304,RMVar_hsa_circ_325291,RMVar_hsa_circ_179552,RMVar_hsa_circ_321816,RMVar_hsa_circ_284628,RMVar_hsa_circ_179556,RMVar_hsa_circ_179557,RMVar_hsa_circ_179555 35961 RMVar_ID_35961 Human_SNP_ID_607423452 A-to-I Human chr16 - 70256373 70256373 70256373 TTGAAACTGGGAGGCAGAGGTTGTGGTGAGCCAAGATCACACCATTGCACTCCAGCCTGAACAAC TTGAAACTGGGAGGCAGAGGTTGTGGTGAGCCGAGATCACACCATTGCACTCCAGCCTGAACAAC T C AARS1 Ensembl:ENSG00000090861 Protein coding intron GSE38233;GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,32596459 RNA-Seq:(High) rs900331376 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_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_46263,RMVar_hsa_circ_179553,RMVar_hsa_circ_179554,RMVar_hsa_circ_290304,RMVar_hsa_circ_325291,RMVar_hsa_circ_179552,RMVar_hsa_circ_321816,RMVar_hsa_circ_284628,RMVar_hsa_circ_179556,RMVar_hsa_circ_179557,RMVar_hsa_circ_179555 35962 RMVar_ID_35962 Human_SNP_ID_607423456 A-to-I Human chr16 - 70256390 70256390 70256390 TGAGGCAAGAGAATCATTTGAAACTGGGAGGCAGAGGTTGTGGTGAGCCAAGATCACACCATTGC TGAGGCAAGAGAATCATTTGAAACTGGGAGGCGGAGGTTGTGGTGAGCCAAGATCACACCATTGC T C AARS1 Ensembl:ENSG00000090861 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,31158229,31158229,32596459,32596459 RNA-Seq:(High) rs1458516182 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17564270 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_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_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_46263,RMVar_hsa_circ_179553,RMVar_hsa_circ_179554,RMVar_hsa_circ_290304,RMVar_hsa_circ_325291,RMVar_hsa_circ_179552,RMVar_hsa_circ_321816,RMVar_hsa_circ_284628,RMVar_hsa_circ_179556,RMVar_hsa_circ_179557,RMVar_hsa_circ_179555 35963 RMVar_ID_35963 Human_SNP_ID_607423683 A-to-I Human chr16 - 70257346 70257346 70257346 TAGTGGCACAGTCTCGGCTCATTGCAACCTCTACCTCCTGGCTTCGATTCTCATGCCTCAGCCTC TAGTGGCACAGTCTCGGCTCATTGCAACCTCTGCCTCCTGGCTTCGATTCTCATGCCTCAGCCTC T C AARS1 Ensembl:ENSG00000090861 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1217710327 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12794720,Human_RBP_ID_25224833 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_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_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_46263,RMVar_hsa_circ_179553,RMVar_hsa_circ_179554,RMVar_hsa_circ_290304,RMVar_hsa_circ_325291,RMVar_hsa_circ_179552,RMVar_hsa_circ_321816,RMVar_hsa_circ_284628,RMVar_hsa_circ_179556,RMVar_hsa_circ_179557,RMVar_hsa_circ_179555 35964 RMVar_ID_35964 Human_SNP_ID_607423692 A-to-I Human chr16 - 70257369 70257369 70257369 GCTCTGTCCCGCAGGGTGGAGTGTAGTGGCACAGTCTCGGCTCATTGCAACCTCTACCTCCTGGC GCTCTGTCCCGCAGGGTGGAGTGTAGTGGCACGGTCTCGGCTCATTGCAACCTCTACCTCCTGGC T C AARS1 Ensembl:ENSG00000090861 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1225593357 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12794721 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_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_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_46263,RMVar_hsa_circ_179553,RMVar_hsa_circ_179554,RMVar_hsa_circ_290304,RMVar_hsa_circ_325291,RMVar_hsa_circ_179552,RMVar_hsa_circ_321816,RMVar_hsa_circ_284628,RMVar_hsa_circ_179556,RMVar_hsa_circ_179557,RMVar_hsa_circ_179555 35965 RMVar_ID_35965 Human_SNP_ID_607424274 A-to-I Human chr16 - 70259154 70259154 70259154 CCCCGACGAAGACCCATCATGAGCAACCACACAGCTACGCACATTCTGAACTTCGCCCTGCGCTC CCCCGACGAAGACCCATCATGAGCAACCACACGGCTACGCACATTCTGAACTTCGCCCTGCGCTC T C AARS1 Ensembl:ENSG00000090861 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs367579673 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5848,Human_RBP_ID_3947883,Human_RBP_ID_6531771,Human_RBP_ID_8231829,Human_RBP_ID_9256836,Human_RBP_ID_9285233,Human_RBP_ID_12794771,Human_RBP_ID_17255190,Human_RBP_ID_22473912 Human_Splice_Rec_1734762,Human_Splice_Rec_1734786,Human_Splice_Rec_1734800,Human_Splice_Rec_1734804,Human_Splice_Rec_1734810 Human_miRNA_ID_2076426,Human_miRNA_ID_2206000 RMVar_hsa_circ_2025,RMVar_hsa_circ_80087,RMVar_hsa_circ_110816,RMVar_hsa_circ_127201,RMVar_hsa_circ_119668,RMVar_hsa_circ_104782,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_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_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_321816,RMVar_hsa_circ_284628,RMVar_hsa_circ_82104,RMVar_hsa_circ_179556,RMVar_hsa_circ_179557,RMVar_hsa_circ_179555,RMVar_hsa_circ_297170,RMVar_hsa_circ_40313,RMVar_hsa_circ_179562,RMVar_hsa_circ_49717,RMVar_hsa_circ_297044,RMVar_hsa_circ_179558,RMVar_hsa_circ_179559,RMVar_hsa_circ_332434,RMVar_hsa_circ_371390,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_179566,RMVar_hsa_circ_179567,RMVar_hsa_circ_179565,RMVar_hsa_circ_179563,RMVar_hsa_circ_179560,RMVar_hsa_circ_179561 35966 RMVar_ID_35966 Human_SNP_ID_607425096 A-to-I Human chr16 - 70261807 70261807 70261807 AAATTAGCCAGGTATGGTGGTGGATGCCTGTAATCCCACCTGCTCGGGAAGCTGAGAGGGGAGAA AAATTAGCCAGGTATGGTGGTGGATGCCTGTAGTCCCACCTGCTCGGGAAGCTGAGAGGGGAGAA T C AARS1 Ensembl:ENSG00000090861 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1325479161 Functional Loss SNV dbSNP153 33..33 33 - - - 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_179570,RMVar_hsa_circ_179572,RMVar_hsa_circ_179573,RMVar_hsa_circ_179571,RMVar_hsa_circ_179568,RMVar_hsa_circ_179569 35967 RMVar_ID_35967 Human_SNP_ID_607425807 A-to-I Human chr16 - 70263765 70263765 70263765 AGGTGTGGTGGCGCATGCCTGTAGTCCCAGCTATTTGTGGGGCTGAGGCAGGAGGATCACTTGAG AGGTGTGGTGGCGCATGCCTGTAGTCCCAGCTGTTTGTGGGGCTGAGGCAGGAGGATCACTTGAG T C AARS1 Ensembl:ENSG00000090861 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs373783148 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12794843,Human_RBP_ID_17564718,Human_RBP_ID_25224886 RMVar_hsa_circ_80087,RMVar_hsa_circ_110816,RMVar_hsa_circ_127201,RMVar_hsa_circ_119668,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_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_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_179576 35968 RMVar_ID_35968 Human_SNP_ID_607426069 A-to-I Human chr16 - 70264596 70264596 70264596 AATGCTATTAGGGGCCTGGCGCTGTGCCTCACACCTGTAATCCCAACACTTTGGGAGGCCGGGGC AATGCTATTAGGGGCCTGGCGCTGTGCCTCACTCCTGTAATCCCAACACTTTGGGAGGCCGGGGC T A AARS1 Ensembl:ENSG00000090861 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1340882661 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80087,RMVar_hsa_circ_110816,RMVar_hsa_circ_127201,RMVar_hsa_circ_119668,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_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_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_179576 35969 RMVar_ID_35969 Human_SNP_ID_607426530 A-to-I Human chr16 - 70265989 70265989 70265989 TATTTTTCCTAGAGACGGGGTTTCACCATGTTAGTCAGGATGGTCTCAATCTCCTGACCTCATGA TATTTTTCCTAGAGACGGGGTTTCACCATGTTTGTCAGGATGGTCTCAATCTCCTGACCTCATGA T A AARS1 Ensembl:ENSG00000090861 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs934498145 Functional Loss SNV dbSNP153 33..33 33 - - - 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_179532,RMVar_hsa_circ_76551,RMVar_hsa_circ_179536,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_324254,RMVar_hsa_circ_286801,RMVar_hsa_circ_101642,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_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_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 35970 RMVar_ID_35970 Human_SNP_ID_607426555 A-to-I Human chr16 - 70266069 70266069 70266069 GACCTCCTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACAGCGCC GACCTCCTGATCCGCCCGCCTCGGCCTCCCAACGTGCTGGGATTACAGGCGTGAGCCACAGCGCC T G AARS1 Ensembl:ENSG00000090861 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1290960590 Functional Loss SNV dbSNP153 33..33 33 - - - 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_179532,RMVar_hsa_circ_76551,RMVar_hsa_circ_179536,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_324254,RMVar_hsa_circ_286801,RMVar_hsa_circ_101642,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_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_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 35971 RMVar_ID_35971 Human_SNP_ID_607428545 A-to-I Human chr16 - 70271890 70271890 70271890 AGATGGGTGACACGGGCCCCTGTGGTCCTTGCAGTGAGATCCACTACGACCGGATTGGTGGTCGG AGATGGGTGACACGGGCCCCTGTGGTCCTTGCTGTGAGATCCACTACGACCGGATTGGTGGTCGG T A AARS1 Ensembl:ENSG00000090861 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1176005208 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5849,Human_RBP_ID_4380851,Human_RBP_ID_8812006,Human_RBP_ID_9257071,Human_RBP_ID_9285884,Human_RBP_ID_12795038,Human_RBP_ID_22441081 Human_Splice_Rec_1734744 Human_miRNA_ID_2506717,Human_miRNA_ID_3043288 RMVar_hsa_circ_110816,RMVar_hsa_circ_127201,RMVar_hsa_circ_82118,RMVar_hsa_circ_179532,RMVar_hsa_circ_76551,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_101642,RMVar_hsa_circ_100575,RMVar_hsa_circ_179560,RMVar_hsa_circ_122626,RMVar_hsa_circ_77343,RMVar_hsa_circ_179570,RMVar_hsa_circ_179568,RMVar_hsa_circ_179569,RMVar_hsa_circ_12494,RMVar_hsa_circ_119896,RMVar_hsa_circ_179580,RMVar_hsa_circ_589,RMVar_hsa_circ_32788,RMVar_hsa_circ_313607,RMVar_hsa_circ_7020,RMVar_hsa_circ_289973,RMVar_hsa_circ_179584,RMVar_hsa_circ_331613 35972 RMVar_ID_35972 Human_SNP_ID_607430716 A-to-I Human chr16 - 70277890 70277890 70277890 AAATTAGCCAGGTGTACCTGTACGTGCCTGTAATCTCAGCTACTTGGGAGGCTGAGGCAAGAGAA AAATTAGCCAGGTGTACCTGTACGTGCCTGTAGTCTCAGCTACTTGGGAGGCTGAGGCAAGAGAA T C AARS1 Ensembl:ENSG00000090861 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs779758589 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110816,RMVar_hsa_circ_82118,RMVar_hsa_circ_179530,RMVar_hsa_circ_179531,RMVar_hsa_circ_101642,RMVar_hsa_circ_179560,RMVar_hsa_circ_12494,RMVar_hsa_circ_32788,RMVar_hsa_circ_313607,RMVar_hsa_circ_289973,RMVar_hsa_circ_179584,RMVar_hsa_circ_281927,RMVar_hsa_circ_331613,RMVar_hsa_circ_47298 35973 RMVar_ID_35973 Human_SNP_ID_607431675 A-to-I Human chr16 - 70281096 70281096 70281096 GCTGGGCGCAGTGGCTCACACTTGTAATCCCAACACTCTGGGAGGCCGAGGCAGATAGGTCACTT GCTGGGCGCAGTGGCTCACACTTGTAATCCCAGCACTCTGGGAGGCCGAGGCAGATAGGTCACTT T C AARS1 Ensembl:ENSG00000090861 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs562341930 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110816,RMVar_hsa_circ_82118,RMVar_hsa_circ_179530,RMVar_hsa_circ_179531,RMVar_hsa_circ_101642,RMVar_hsa_circ_179560,RMVar_hsa_circ_12494,RMVar_hsa_circ_32788,RMVar_hsa_circ_313607,RMVar_hsa_circ_289973,RMVar_hsa_circ_179584,RMVar_hsa_circ_281927,RMVar_hsa_circ_331613,RMVar_hsa_circ_47298 35974 RMVar_ID_35974 Human_SNP_ID_607431922 A-to-I Human chr16 - 70281962 70281962 70281962 TATTTTTAGTAGAGATGGGGTTTCACCGTGTTAGCCAGGATGGTCTCAATCTCCTGACCTTGTGA TATTTTTAGTAGAGATGGGGTTTCACCGTGTTGGCCAGGATGGTCTCAATCTCCTGACCTTGTGA T C AARS1 Ensembl:ENSG00000090861 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1201838566 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110816,RMVar_hsa_circ_82118,RMVar_hsa_circ_179530,RMVar_hsa_circ_179531,RMVar_hsa_circ_101642,RMVar_hsa_circ_179560,RMVar_hsa_circ_12494,RMVar_hsa_circ_32788,RMVar_hsa_circ_313607,RMVar_hsa_circ_289973,RMVar_hsa_circ_179584,RMVar_hsa_circ_281927,RMVar_hsa_circ_331613,RMVar_hsa_circ_47298 35975 RMVar_ID_35975 Human_SNP_ID_607432805 A-to-I Human chr16 - 70284438 70284438 70284438 GCCACCATGCCCGGATTATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTAGCCAAGA GCCACCATGCCCGGATTATTTTTTGTATTTTTGGTAGAGACGGGGTTTCACCATGTTAGCCAAGA T C AARS1 Ensembl:ENSG00000090861 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560624183 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25225031 RMVar_hsa_circ_82118,RMVar_hsa_circ_179530 35976 RMVar_ID_35976 Human_SNP_ID_607433004 A-to-I Human chr16 - 70285134 70285134 70285134 ACCACTATTTCCCAGGTTCAAGCGATTCTCCCATCTCAGCCTTCTGAGTAGCTGGGATTACAGGC ACCACTATTTCCCAGGTTCAAGCGATTCTCCCGTCTCAGCCTTCTGAGTAGCTGGGATTACAGGC T C AARS1 Ensembl:ENSG00000090861 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs8063749 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82118,RMVar_hsa_circ_179530 35977 RMVar_ID_35977 Human_SNP_ID_607433477 A-to-I Human chr16 - 70286648 70286648 70286648 TATTTTTAGTAGAGACAGGGTTTCACCGTGTTAGCCAGGATGGTCTTGATCTCCTGACCTTGTGA TATTTTTAGTAGAGACAGGGTTTCACCGTGTTGGCCAGGATGGTCTTGATCTCCTGACCTTGTGA T C AARS1 Ensembl:ENSG00000090861 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1372299772 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82118,RMVar_hsa_circ_179530 35978 RMVar_ID_35978 Human_SNP_ID_607433483 A-to-I Human chr16 - 70286664 70286664 70286664 ATTTTTTGTTGTGTTGTATTTTTAGTAGAGACAGGGTTTCACCGTGTTAGCCAGGATGGTCTTGA ATTTTTTGTTGTGTTGTATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGGTCTTGA T C AARS1 Ensembl:ENSG00000090861 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs976662175 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82118,RMVar_hsa_circ_179530 35979 RMVar_ID_35979 Human_SNP_ID_607444726 A-to-I Human chr16 + 70327293 70327293 70327293 ATGGTGGCTCATGCCTGTAATCCCAGCACTTTAGCAGGCCGAGGTGGGTGGATCACGAGGTCAGG ATGGTGGCTCATGCCTGTAATCCCAGCACTTTGGCAGGCCGAGGTGGGTGGATCACGAGGTCAGG A G DDX19B,AC012184.2 Ensembl:ENSG00000157349,Ensembl:ENSG00000260537 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1247362264 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18041,RMVar_hsa_circ_19275,RMVar_hsa_circ_73023,RMVar_hsa_circ_343867,RMVar_hsa_circ_84694,RMVar_hsa_circ_107049,RMVar_hsa_circ_179589,RMVar_hsa_circ_179590,RMVar_hsa_circ_110877,RMVar_hsa_circ_25997,RMVar_hsa_circ_179591,RMVar_hsa_circ_299142,RMVar_hsa_circ_116969,RMVar_hsa_circ_179593 35980 RMVar_ID_35980 Human_SNP_ID_607444899 A-to-I Human chr16 - 70327925 70327925 70327925 CTGGTCTCGAACTCCTAACCTTACAATGATCCACCCACCTTAGGCTCCCAAAGTGCTGAGATTAC CTGGTCTCGAACTCCTAACCTTACAATGATCCGCCCACCTTAGGCTCCCAAAGTGCTGAGATTAC T C AC012184.3 Ensembl:ENSG00000261777 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1300093925 Functional Loss SNV dbSNP153 33..33 33 - - - 35981 RMVar_ID_35981 Human_SNP_ID_607446932 A-to-I Human chr16 + 70335528 70335528 70335528 CAGGCTGGAGTGCCGTGGCACGACCTCGGCTCACTGTAACCTCTGCCTCCCAGGTTCAAGCGATT CAGGCTGGAGTGCCGTGGCACGACCTCGGCTCGCTGTAACCTCTGCCTCCCAGGTTCAAGCGATT A G AC012184.2 Ensembl:ENSG00000260537 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270280876 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73023,RMVar_hsa_circ_343867,RMVar_hsa_circ_179590,RMVar_hsa_circ_110877 35982 RMVar_ID_35982 Human_SNP_ID_607447714 A-to-I Human chr16 + 70338622 70338621 70338622 GTTGGCCAGACCGGTCTCGAACTCCTGGCCTCAAGCGAGCAACTCACCTCGGCCTCCCAAAGTGC GTTGGCCAGACCGGTCTCGAACTCCTGGCCTC_AGCGAGCAACTCACCTCGGCCTCCCAAAGTGC CA C AC012184.2 Ensembl:ENSG00000260537 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355531349 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_73023,RMVar_hsa_circ_343867,RMVar_hsa_circ_179590,RMVar_hsa_circ_110877 35983 RMVar_ID_35983 Human_SNP_ID_607449172 A-to-I Human chr16 + 70343461 70343461 70343461 AAAACAGAAGTGGGCCTGGCTCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGT AAAACAGAAGTGGGCCTGGCTCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGT A G AC012184.2 Ensembl:ENSG00000260537 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs938603790 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73023,RMVar_hsa_circ_343867,RMVar_hsa_circ_179590,RMVar_hsa_circ_110877 35984 RMVar_ID_35984 Human_SNP_ID_607453179 A-to-I Human chr16 + 70357070 70357070 70357070 GGAGTTCAAGACCAGCCTGACCAACATGGTGAAACCCTGTCTCCACTAAAAATACAAAACTCAAA GGAGTTCAAGACCAGCCTGACCAACATGGTGACACCCTGTCTCCACTAAAAATACAAAACTCAAA A C DDX19A,AC012184.2 Ensembl:ENSG00000168872,Ensembl:ENSG00000260537 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1467908417 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23165197 RMVar_hsa_circ_73023,RMVar_hsa_circ_179590,RMVar_hsa_circ_110877,RMVar_hsa_circ_45779,RMVar_hsa_circ_104389,RMVar_hsa_circ_179594,RMVar_hsa_circ_297588 35985 RMVar_ID_35985 Human_SNP_ID_607453575 A-to-I Human chr16 + 70358170 70358170 70358170 CTCGTTCCTCAGCCTCTCACGTAGCTGGGATTACAGGCCTGAGCCACCACACCTGGCTAATTTTG CTCGTTCCTCAGCCTCTCACGTAGCTGGGATTGCAGGCCTGAGCCACCACACCTGGCTAATTTTG A G DDX19A,AC012184.2 Ensembl:ENSG00000168872,Ensembl:ENSG00000260537 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs910588220 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73023,RMVar_hsa_circ_179590,RMVar_hsa_circ_110877,RMVar_hsa_circ_45779,RMVar_hsa_circ_104389,RMVar_hsa_circ_179594,RMVar_hsa_circ_297588 35986 RMVar_ID_35986 Human_SNP_ID_607453576 A-to-I Human chr16 + 70358172 70358172 70358172 CGTTCCTCAGCCTCTCACGTAGCTGGGATTACAGGCCTGAGCCACCACACCTGGCTAATTTTGGT CGTTCCTCAGCCTCTCACGTAGCTGGGATTACGGGCCTGAGCCACCACACCTGGCTAATTTTGGT A G DDX19A,AC012184.2 Ensembl:ENSG00000168872,Ensembl:ENSG00000260537 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs923766856 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73023,RMVar_hsa_circ_179590,RMVar_hsa_circ_110877,RMVar_hsa_circ_45779,RMVar_hsa_circ_104389,RMVar_hsa_circ_179594,RMVar_hsa_circ_297588 35987 RMVar_ID_35987 Human_SNP_ID_607453727 A-to-I Human chr16 + 70358740 70358740 70358740 TAATGGCACATGGCTTGTAGTCCCGGCTACTCAGGAGGCTGAGGTAGGAGAATTGCTTGAACCCA TAATGGCACATGGCTTGTAGTCCCGGCTACTCGGGAGGCTGAGGTAGGAGAATTGCTTGAACCCA A G DDX19A,AC012184.2 Ensembl:ENSG00000168872,Ensembl:ENSG00000260537 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1274000010 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73023,RMVar_hsa_circ_179590,RMVar_hsa_circ_110877,RMVar_hsa_circ_45779,RMVar_hsa_circ_104389,RMVar_hsa_circ_179594,RMVar_hsa_circ_297588 35988 RMVar_ID_35988 Human_SNP_ID_607453735 A-to-I Human chr16 + 70358772 70358772 70358772 AGGAGGCTGAGGTAGGAGAATTGCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCCGAGATCATG AGGAGGCTGAGGTAGGAGAATTGCTTGAACCCGGGAGGCGGAGGTTGCAGTGAGCCGAGATCATG A G DDX19A,AC012184.2 Ensembl:ENSG00000168872,Ensembl:ENSG00000260537 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1231812465 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73023,RMVar_hsa_circ_179590,RMVar_hsa_circ_110877,RMVar_hsa_circ_45779,RMVar_hsa_circ_104389,RMVar_hsa_circ_179594,RMVar_hsa_circ_297588 35989 RMVar_ID_35989 Human_SNP_ID_607454072 A-to-I Human chr16 + 70360187 70360187 70360187 CCTGTAATCCTAGCTCCTCAGAAGGCTGAGGTAGGAGACTCGCTTGAACCCAGGAGGCAGAGGTT CCTGTAATCCTAGCTCCTCAGAAGGCTGAGGTTGGAGACTCGCTTGAACCCAGGAGGCAGAGGTT A T DDX19A,AC012184.2 Ensembl:ENSG00000168872,Ensembl:ENSG00000260537 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1276585391 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73023,RMVar_hsa_circ_179590,RMVar_hsa_circ_110877,RMVar_hsa_circ_45779,RMVar_hsa_circ_104389,RMVar_hsa_circ_179594,RMVar_hsa_circ_297588 35990 RMVar_ID_35990 Human_SNP_ID_607454533 A-to-I Human chr16 + 70361889 70361889 70361889 CAAAACCCTGTCTCTACTAAAAATACAAAATTAGCTGGGCACGGTGGCCCAAACCTGTAATCCTA CAAAACCCTGTCTCTACTAAAAATACAAAATTTGCTGGGCACGGTGGCCCAAACCTGTAATCCTA A T DDX19A,AC012184.2 Ensembl:ENSG00000168872,Ensembl:ENSG00000260537 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1157543280 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73023,RMVar_hsa_circ_104389,RMVar_hsa_circ_179594,RMVar_hsa_circ_85894,RMVar_hsa_circ_309277,RMVar_hsa_circ_179597,RMVar_hsa_circ_179598,RMVar_hsa_circ_179599 35991 RMVar_ID_35991 Human_SNP_ID_607454595 A-to-I Human chr16 + 70362032 70362032 70362032 GTCTTACTAAAATCAAAAAAAAAAAAATATCCAGGCCTGTTGGCATGTGCCTGTAGTCCCAGCTA GTCTTACTAAAATCAAAAAAAAAAAAATATCCGGGCCTGTTGGCATGTGCCTGTAGTCCCAGCTA A G DDX19A,AC012184.2 Ensembl:ENSG00000168872,Ensembl:ENSG00000260537 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1462008222 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73023,RMVar_hsa_circ_104389,RMVar_hsa_circ_179594,RMVar_hsa_circ_85894,RMVar_hsa_circ_309277,RMVar_hsa_circ_179597,RMVar_hsa_circ_179598,RMVar_hsa_circ_179599 35992 RMVar_ID_35992 Human_SNP_ID_607457928 A-to-I Human chr16 + 70373138 70373138 70373138 CACGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGTAGGAGGATCGCTTGAGCCTGGGTAGAGGC CACGCCTGTAGTCCCAGCTACTCGGGAGGCTGTGGTAGGAGGATCGCTTGAGCCTGGGTAGAGGC A T DDX19A Ensembl:ENSG00000168872 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs747691798 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26445319 35993 RMVar_ID_35993 Human_SNP_ID_607457939 A-to-I Human chr16 + 70373165 70373165 70373165 GGCTGAGGTAGGAGGATCGCTTGAGCCTGGGTAGAGGCTGCTGTGAGCTGAAATGGCGCCACTGC GGCTGAGGTAGGAGGATCGCTTGAGCCTGGGTGGAGGCTGCTGTGAGCTGAAATGGCGCCACTGC A G DDX19A Ensembl:ENSG00000168872 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1387824087 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_478781,Human_RBP_ID_25225304,Human_RBP_ID_26445319 35994 RMVar_ID_35994 Human_SNP_ID_607458138 A-to-I Human chr16 + 70373778 70373778 70373778 TTTTGAGACAGAGTGTCACTCTGGCCCGGAGTACAGAGGCGTGATCTCGGCCCACTGCAACCTCT TTTTGAGACAGAGTGTCACTCTGGCCCGGAGTGCAGAGGCGTGATCTCGGCCCACTGCAACCTCT A G - - Other Unknown GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 29129909,30559470 RNA-Seq:(High) rs894018057 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12796178 35995 RMVar_ID_35995 Human_SNP_ID_607458177 A-to-I Human chr16 + 70373886 70373886 70373886 AGCTGGGATTACAGGCACATGCCAGCATGCCCAGCTAATCTTTATATTTTCTGTAGAGATGGGGT AGCTGGGATTACAGGCACATGCCAGCATGCCCGGCTAATCTTTATATTTTCTGTAGAGATGGGGT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1567660997 Functional Loss SNV dbSNP153 33..33 33 - - - 35996 RMVar_ID_35996 Human_SNP_ID_607458183 A-to-I Human chr16 + 70373897 70373897 70373897 CAGGCACATGCCAGCATGCCCAGCTAATCTTTATATTTTCTGTAGAGATGGGGTTTTGCCATGTT CAGGCACATGCCAGCATGCCCAGCTAATCTTTCTATTTTCTGTAGAGATGGGGTTTTGCCATGTT A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913166061 Functional Loss SNV dbSNP153 33..33 33 - - - 35997 RMVar_ID_35997 Human_SNP_ID_607458423 A-to-I Human chr16 + 70374601 70374600 70374602 ATCTCGGTTCACTGCAGCCTCGACCCAGTCTCAAGTGACCCTCCTGCCTCACCCCTCCAAGTAGA ATCTCGGTTCACTGCAGCCTCGACCCAGTCTC__GTGACCCTCCTGCCTCACCCCTCCAAGTAGA CAA C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1296103666 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_6532069,Human_RBP_ID_12796215 35998 RMVar_ID_35998 Human_SNP_ID_607458435 A-to-I Human chr16 + 70374651 70374651 70374651 ACCCCTCCAAGTAGATGGGACTACAGGCCTGCACCACCACACCCGGCTAATTTTTGTATTTTTTT ACCCCTCCAAGTAGATGGGACTACAGGCCTGCGCCACCACACCCGGCTAATTTTTGTATTTTTTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1365111760 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12796217 35999 RMVar_ID_35999 Human_SNP_ID_607458462 A-to-I Human chr16 + 70374743 70374743 70374743 CCGAGGCTGGTTTTGAACTCCTGAGCTTAAGTAATCTGCCCGCCTGGGCCTCCCAAAGTGCTGGG CCGAGGCTGGTTTTGAACTCCTGAGCTTAAGTGATCTGCCCGCCTGGGCCTCCCAAAGTGCTGGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs933055230 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12796223 36000 RMVar_ID_36000 Human_SNP_ID_607458612 A-to-I Human chr16 + 70375329 70375329 70375329 TTTAGTAGAGATGGGGTTTCTCTATGTTGGTCAGTCTGGTCTTGAACTCCCAACCTCAAGCGAAC TTTAGTAGAGATGGGGTTTCTCTATGTTGGTCGGTCTGGTCTTGAACTCCCAACCTCAAGCGAAC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1306669539 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1238248,Human_RBP_ID_12796241 36001 RMVar_ID_36001 Human_SNP_ID_607459039 A-to-I Human chr16 - 70376778 70376777 70376779 AGATTGAGCCACTGCACTCCAGCCTGAGCGACAGAGTAAGACTCCGTCTCAAAAAAAAAAAAGTA AGATTGAGCCACTGCACTCCAGCCTGAGCGA__GAGTAAGACTCCGTCTCAAAAAAAAAAAAGTA CTG C ST3GAL2 Ensembl:ENSG00000157350 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1404581110 Functional Loss DEL dbSNP153 32..33 33 - - - 36002 RMVar_ID_36002 Human_SNP_ID_607459063 A-to-I Human chr16 - 70376825 70376825 70376825 AGGCAGAGAATTGCTTGAACCTGGGAGGTGGAAGTTGTGGTGAGCCGAGATTGAGCCACTGCACT AGGCAGAGAATTGCTTGAACCTGGGAGGTGGAGGTTGTGGTGAGCCGAGATTGAGCCACTGCACT T C ST3GAL2 Ensembl:ENSG00000157350 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs557036067 Functional Loss SNV dbSNP153 33..33 33 - - - 36003 RMVar_ID_36003 Human_SNP_ID_607459163 A-to-I Human chr16 - 70377171 70377169 70377171 TTTTTTTTTTTTTTTTTTTTTTTTTAAGAGACAGGGTCTCCTGTCGCCCAGACTGGTGCAGAGCT TTTTTTTTTTTTTTTTTTTTTTTTTAAGAGAC__GGTCTCCTGTCGCCCAGACTGGTGCAGAGCT CCT C ST3GAL2 Ensembl:ENSG00000157350 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1326026865 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_12796319,Human_RBP_ID_17565122 36004 RMVar_ID_36004 Human_SNP_ID_607459593 A-to-I Human chr16 - 70378221 70378221 70378221 TTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCACAGGTCATC TTTAGTAGAGACGGGGTTTCACCATGTTGGCCGGGCTGGTCTCGAACTCCTGACCACAGGTCATC T C ST3GAL2 Ensembl:ENSG00000157350 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202651737 Functional Loss SNV dbSNP153 33..33 33 - - - 36005 RMVar_ID_36005 Human_SNP_ID_607459605 A-to-I Human chr16 - 70378250 70378250 70378250 TGCCACCACACCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGC TGCCACCACACCCAGCTAATTTTTGTATTTTTGGTAGAGACGGGGTTTCACCATGTTGGCCAGGC T C ST3GAL2 Ensembl:ENSG00000157350 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs367949450 Functional Loss SNV dbSNP153 33..33 33 - - - 36006 RMVar_ID_36006 Human_SNP_ID_607459625 A-to-I Human chr16 - 70378312 70378312 70378312 GCAACCTCCGCCTCCCAAGTTCACCCACCTCAACCTCCCGAGTAGCTGGAATTACAGGGGTGTGC GCAACCTCCGCCTCCCAAGTTCACCCACCTCAGCCTCCCGAGTAGCTGGAATTACAGGGGTGTGC T C ST3GAL2 Ensembl:ENSG00000157350 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs779075576 Functional Loss SNV dbSNP153 33..33 33 - - - 36007 RMVar_ID_36007 Human_SNP_ID_607459626 A-to-I Human chr16 - 70378312 70378312 70378312 GCAACCTCCGCCTCCCAAGTTCACCCACCTCAACCTCCCGAGTAGCTGGAATTACAGGGGTGTGC GCAACCTCCGCCTCCCAAGTTCACCCACCTCACCCTCCCGAGTAGCTGGAATTACAGGGGTGTGC T G ST3GAL2 Ensembl:ENSG00000157350 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs779075576 Functional Loss SNV dbSNP153 33..33 33 - - - 36008 RMVar_ID_36008 Human_SNP_ID_607459628 A-to-I Human chr16 - 70378313 70378313 70378313 TGCAACCTCCGCCTCCCAAGTTCACCCACCTCAACCTCCCGAGTAGCTGGAATTACAGGGGTGTG TGCAACCTCCGCCTCCCAAGTTCACCCACCTCCACCTCCCGAGTAGCTGGAATTACAGGGGTGTG T G ST3GAL2 Ensembl:ENSG00000157350 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1292434592 Functional Loss SNV dbSNP153 33..33 33 - - - 36009 RMVar_ID_36009 Human_SNP_ID_607459927 A-to-I Human chr16 - 70378959 70378959 70378959 GAGTCTTGTTCTGTTACCCAGGCTGGAGTGCAATGGCCCGATGTCGGCTCATCCCAACCTCCACC GAGTCTTGTTCTGTTACCCAGGCTGGAGTGCAGTGGCCCGATGTCGGCTCATCCCAACCTCCACC T C ST3GAL2 Ensembl:ENSG00000157350 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs117025305 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2481406,Human_RBP_ID_12796337,Human_RBP_ID_23165224,Human_RBP_ID_25225347 Human_miRNA_ID_1075396 36010 RMVar_ID_36010 Human_SNP_ID_607459937 A-to-I Human chr16 - 70378992 70378992 70378992 TTTATTTATTTAATTTATTTATTTATTGAGACAGAGTCTTGTTCTGTTACCCAGGCTGGAGTGCA TTTATTTATTTAATTTATTTATTTATTGAGACGGAGTCTTGTTCTGTTACCCAGGCTGGAGTGCA T C ST3GAL2 Ensembl:ENSG00000157350 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1247765235 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2481407,Human_RBP_ID_6532096,Human_RBP_ID_8437916 36011 RMVar_ID_36011 Human_SNP_ID_607460125 A-to-I Human chr16 - 70379472 70379472 70379472 GTCCTTCATTGTTCTGAAATGGGCATGATGGAAGAAGGCGGGTCTGGTAGGATAGCTGTGACTGA GTCCTTCATTGTTCTGAAATGGGCATGATGGAGGAAGGCGGGTCTGGTAGGATAGCTGTGACTGA T C ST3GAL2 Ensembl:ENSG00000157350 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1411955562 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2481410,Human_RBP_ID_3498487,Human_RBP_ID_6532106 RMVar_hsa_circ_125819,RMVar_hsa_circ_179603 36012 RMVar_ID_36012 Human_SNP_ID_607460242 A-to-I Human chr16 - 70379795 70379795 70379795 AAACCTCGTCTCTACCAAAAAAAAAAAAAAATACAAAAATTAGCCAGGCGCAGTGGTGCGCACCT AAACCTCGTCTCTACCAAAAAAAAAAAAAAATGCAAAAATTAGCCAGGCGCAGTGGTGCGCACCT T C ST3GAL2 Ensembl:ENSG00000157350 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1051706406 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12796381,Human_RBP_ID_25225353 RMVar_hsa_circ_125819,RMVar_hsa_circ_179603 36013 RMVar_ID_36013 Human_SNP_ID_607462047 A-to-I Human chr16 - 70384539 70384539 70384539 CACCACACCCAGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTTACCATGTTGGCCAGGATGG CACCACACCCAGCTAATTTTTGTATTTTTAGTGGAGACAGGGTTTTACCATGTTGGCCAGGATGG T C ST3GAL2 Ensembl:ENSG00000157350 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs902973980 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102862,RMVar_hsa_circ_179605 36014 RMVar_ID_36014 Human_SNP_ID_607462252 A-to-I Human chr16 - 70385116 70385116 70385116 TATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCTAGGATGGTCTCGATCTCCTGACCTTGTGA TATTTTTAGTAGAGACGGGGTTTCACCGTGTTGGCTAGGATGGTCTCGATCTCCTGACCTTGTGA T C ST3GAL2 Ensembl:ENSG00000157350 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1264508776 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102862,RMVar_hsa_circ_179605 36015 RMVar_ID_36015 Human_SNP_ID_607462294 A-to-I Human chr16 - 70385257 70385257 70385257 GAGTCTCACTCTGTCACCCAGGCTGGAGTGCAATGGCGCCTTCTCGGCTCACTGCAACCTGGGTT GAGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGCGCCTTCTCGGCTCACTGCAACCTGGGTT T C ST3GAL2 Ensembl:ENSG00000157350 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs898889723 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102862,RMVar_hsa_circ_179605 36016 RMVar_ID_36016 Human_SNP_ID_607462530 A-to-I Human chr16 - 70385966 70385966 70385966 GCAGTGGCTCACACCTGTAATCCCAGCACTCTAGGAGGCCAAGGAGGGTAGATTGTTTGAGTCCA GCAGTGGCTCACACCTGTAATCCCAGCACTCTTGGAGGCCAAGGAGGGTAGATTGTTTGAGTCCA T A ST3GAL2 Ensembl:ENSG00000157350 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs368169921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17563807 RMVar_hsa_circ_102862,RMVar_hsa_circ_179605 36017 RMVar_ID_36017 Human_SNP_ID_607462577 A-to-I Human chr16 - 70386099 70386099 70386099 GGAGAATCGCTCGAACCTGGGAGGCAGAGGTTACAGTGAGACGAGATTGTGCCACTGCATTCAAG GGAGAATCGCTCGAACCTGGGAGGCAGAGGTTGCAGTGAGACGAGATTGTGCCACTGCATTCAAG T C ST3GAL2 Ensembl:ENSG00000157350 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1213814200 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102862,RMVar_hsa_circ_179605 36018 RMVar_ID_36018 Human_SNP_ID_607462593 A-to-I Human chr16 - 70386126 70386126 70386126 GTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTCGAACCTGGGAGGCAGAGGTTACAGTG GTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAGTCGCTCGAACCTGGGAGGCAGAGGTTACAGTG T C ST3GAL2 Ensembl:ENSG00000157350 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs932924030 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102862,RMVar_hsa_circ_179605 36019 RMVar_ID_36019 Human_SNP_ID_607462594 A-to-I Human chr16 - 70386126 70386126 70386126 GTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTCGAACCTGGGAGGCAGAGGTTACAGTG GTCCCAGCTACTTGGGAGGCTGAGGCAGGAGACTCGCTCGAACCTGGGAGGCAGAGGTTACAGTG T G ST3GAL2 Ensembl:ENSG00000157350 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs932924030 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102862,RMVar_hsa_circ_179605 36020 RMVar_ID_36020 Human_SNP_ID_607462815 A-to-I Human chr16 - 70386839 70386839 70386839 GAGTTAGAGACCAGCCTGGCCAACATGGTGAAACCTCATCTGTACTAAAAATAAAACAATTAGCT GAGTTAGAGACCAGCCTGGCCAACATGGTGAATCCTCATCTGTACTAAAAATAAAACAATTAGCT T A ST3GAL2 Ensembl:ENSG00000157350 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1257026960 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102862,RMVar_hsa_circ_179605 36021 RMVar_ID_36021 Human_SNP_ID_607462822 A-to-I Human chr16 - 70386873 70386873 70386873 TTGGGAGGCCAAGGCGGGTGGATCACAAGGTCAGGAGTTAGAGACCAGCCTGGCCAACATGGTGA TTGGGAGGCCAAGGCGGGTGGATCACAAGGTCGGGAGTTAGAGACCAGCCTGGCCAACATGGTGA T C ST3GAL2 Ensembl:ENSG00000157350 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1448060263 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102862,RMVar_hsa_circ_179605 36022 RMVar_ID_36022 Human_SNP_ID_607465549 A-to-I Human chr16 - 70396483 70396483 70396483 CCTCCCACCTCAGCTTCAGAGTAGCTGGGACTACAGGCACGTGCCACCACGCCTGGCTAATTTTT CCTCCCACCTCAGCTTCAGAGTAGCTGGGACTTCAGGCACGTGCCACCACGCCTGGCTAATTTTT T A ST3GAL2 Ensembl:ENSG00000157350 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs918197124 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102862,RMVar_hsa_circ_179605 36023 RMVar_ID_36023 Human_SNP_ID_607465865 A-to-I Human chr16 - 70397561 70397561 70397561 CCACCCCTCTCAGCTAATTTTTTTGTATTTTTAGTACAGACGGGGTTTCACCATGTTGGCCAGGC CCACCCCTCTCAGCTAATTTTTTTGTATTTTTGGTACAGACGGGGTTTCACCATGTTGGCCAGGC T C ST3GAL2 Ensembl:ENSG00000157350 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs960695822 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102862,RMVar_hsa_circ_179605 36024 RMVar_ID_36024 Human_SNP_ID_607467150 A-to-I Human chr16 - 70401827 70401827 70401827 ACAACGCCTGGCTGATTTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGG ACAACGCCTGGCTGATTTTTTGTATTTTTAGTGGAGATGGGGTTTCACCATGTTGGCCAGGCTGG T C ST3GAL2 Ensembl:ENSG00000157350 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs929205977 Functional Loss SNV dbSNP153 33..33 33 - - - 36025 RMVar_ID_36025 Human_SNP_ID_607467458 A-to-I Human chr16 - 70402681 70402681 70402681 CACGCCACTGCACTCCAGCCTGGTGACAGAGCAAGACTCCGTCTCAAAAGAAAAAAAAATACTTC CACGCCACTGCACTCCAGCCTGGTGACAGAGCGAGACTCCGTCTCAAAAGAAAAAAAAATACTTC T C ST3GAL2 Ensembl:ENSG00000157350 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs140284469 Functional Loss SNV dbSNP153 33..33 33 - - - 36026 RMVar_ID_36026 Human_SNP_ID_607467459 A-to-I Human chr16 - 70402681 70402681 70402681 CACGCCACTGCACTCCAGCCTGGTGACAGAGCAAGACTCCGTCTCAAAAGAAAAAAAAATACTTC CACGCCACTGCACTCCAGCCTGGTGACAGAGCCAGACTCCGTCTCAAAAGAAAAAAAAATACTTC T G ST3GAL2 Ensembl:ENSG00000157350 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs140284469 Functional Loss SNV dbSNP153 33..33 33 - - - 36027 RMVar_ID_36027 Human_SNP_ID_607469573 A-to-I Human chr16 - 70409482 70409482 70409482 AAAATTAGCCAGGCATGGTGGCGCATGCCTGTAATCCCAGCTACTCAGGAGACCGAGGCAGGAAA AAAATTAGCCAGGCATGGTGGCGCATGCCTGTGATCCCAGCTACTCAGGAGACCGAGGCAGGAAA T C ST3GAL2 Ensembl:ENSG00000157350 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1206257332 Functional Loss SNV dbSNP153 33..33 33 - - - 36028 RMVar_ID_36028 Human_SNP_ID_607469718 A-to-I Human chr16 - 70409867 70409867 70409867 CTTGGGAGGCTGAGGCAGGAGTCTGAGAGTTCAAGTCCAGCCTGGGGAACATAGCAAGACCCTGT CTTGGGAGGCTGAGGCAGGAGTCTGAGAGTTCGAGTCCAGCCTGGGGAACATAGCAAGACCCTGT T C ST3GAL2 Ensembl:ENSG00000157350 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1473529588 Functional Loss SNV dbSNP153 33..33 33 - - - 36029 RMVar_ID_36029 Human_SNP_ID_607469907 A-to-I Human chr16 - 70410383 70410383 70410383 AGCCGGGCATGGTGGTGGGCACCTGTGGTCCCAGCTACGGGGGAGGCTGAGGCAGGAGAATGGCA AGCCGGGCATGGTGGTGGGCACCTGTGGTCCCCGCTACGGGGGAGGCTGAGGCAGGAGAATGGCA T G ST3GAL2 Ensembl:ENSG00000157350 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1258982482 Functional Loss SNV dbSNP153 33..33 33 - - - 36030 RMVar_ID_36030 Human_SNP_ID_607469940 A-to-I Human chr16 - 70410449 70410449 70410449 GGAGATCAAGACCATCCTGGCTAACATGGTGAAGCCCTGTCTCTACTAAAAATACAAAAAAAAAT GGAGATCAAGACCATCCTGGCTAACATGGTGAGGCCCTGTCTCTACTAAAAATACAAAAAAAAAT T C ST3GAL2 Ensembl:ENSG00000157350 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1037788114 Functional Loss SNV dbSNP153 33..33 33 - - - 36031 RMVar_ID_36031 Human_SNP_ID_607470376 A-to-I Human chr16 - 70411870 70411870 70411870 CCCACCTCACCCTCCTGAGTAGCTGGGATTACAGACATCCGCCACCACACCCAGCTAATTTTGTA CCCACCTCACCCTCCTGAGTAGCTGGGATTACGGACATCCGCCACCACACCCAGCTAATTTTGTA T C ST3GAL2 Ensembl:ENSG00000157350 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs993820414 Functional Loss SNV dbSNP153 33..33 33 - - - 36032 RMVar_ID_36032 Human_SNP_ID_607470380 A-to-I Human chr16 - 70411882 70411882 70411882 TCAAGCGATTCTCCCACCTCACCCTCCTGAGTAGCTGGGATTACAGACATCCGCCACCACACCCA TCAAGCGATTCTCCCACCTCACCCTCCTGAGTGGCTGGGATTACAGACATCCGCCACCACACCCA T C ST3GAL2 Ensembl:ENSG00000157350 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs536604872 Functional Loss SNV dbSNP153 33..33 33 - - - 36033 RMVar_ID_36033 Human_SNP_ID_607470538 A-to-I Human chr16 - 70412544 70412544 70412544 GACCTGCCAGGCTCAGGTGATCCTCCCACCTCAGCCTCCTGAGTAGCTGGGCCTACAGAAACATG GACCTGCCAGGCTCAGGTGATCCTCCCACCTCCGCCTCCTGAGTAGCTGGGCCTACAGAAACATG T G ST3GAL2 Ensembl:ENSG00000157350 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1166778165 Functional Loss SNV dbSNP153 33..33 33 - - - 36034 RMVar_ID_36034 Human_SNP_ID_607470651 A-to-I Human chr16 - 70412992 70412992 70412992 CACCTGCCTCCGCCTCCCAAAGTACTGGGATTACAGGTGTGTGCCACCGTGCCCAGCCTCAAGCC CACCTGCCTCCGCCTCCCAAAGTACTGGGATTGCAGGTGTGTGCCACCGTGCCCAGCCTCAAGCC T C ST3GAL2 Ensembl:ENSG00000157350 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1168667880 Functional Loss SNV dbSNP153 33..33 33 - - - 36035 RMVar_ID_36035 Human_SNP_ID_607470703 A-to-I Human chr16 - 70413198 70413198 70413198 TTGCCCAGGCTGGAGTGCAGTGGCCCGATCTTAGCTCACTGCAACCTCCGCCTTCCAGGTTCAAG TTGCCCAGGCTGGAGTGCAGTGGCCCGATCTTGGCTCACTGCAACCTCCGCCTTCCAGGTTCAAG T C ST3GAL2 Ensembl:ENSG00000157350 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971296105 Functional Loss SNV dbSNP153 33..33 33 - - - 36036 RMVar_ID_36036 Human_SNP_ID_607470737 A-to-I Human chr16 - 70413300 70413299 70413300 ATGATCCTGCCCCCTCAGCTTCCCGAGTAGCTAGGGCTGTAGGCACTTGCCACCATGCCCAGCTA ATGATCCTGCCCCCTCAGCTTCCCGAGTAGCT_GGGCTGTAGGCACTTGCCACCATGCCCAGCTA CT C ST3GAL2 Ensembl:ENSG00000157350 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1292163823 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_12796597 36037 RMVar_ID_36037 Human_SNP_ID_607474328 A-to-I Human chr16 - 70425650 70425650 70425650 GAATGGAGCGGTCTCGGTTCACTGCAGCTTCCACCTCTCGGGTTCAAGCGATTCTCCTGTGTCAG GAATGGAGCGGTCTCGGTTCACTGCAGCTTCCGCCTCTCGGGTTCAAGCGATTCTCCTGTGTCAG T C ST3GAL2 Ensembl:ENSG00000157350 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs762329375 Functional Loss SNV dbSNP153 33..33 33 - - - 36038 RMVar_ID_36038 Human_SNP_ID_607474671 A-to-I Human chr16 - 70426446 70426446 70426446 CCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGCGGATTGCCTGAGGTCAGGAGTTCAAGACC CCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGGATTGCCTGAGGTCAGGAGTTCAAGACC T C ST3GAL2 Ensembl:ENSG00000157350 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1235478397 Functional Loss SNV dbSNP153 33..33 33 - - - 36039 RMVar_ID_36039 Human_SNP_ID_607475663 A-to-I Human chr16 - 70429720 70429720 70429720 GGAGAATCACTTGAACCTGGGAGGTGGAGGTTACAGTGAGCCGTGATCACCCCATTTCACTCCAG GGAGAATCACTTGAACCTGGGAGGTGGAGGTTCCAGTGAGCCGTGATCACCCCATTTCACTCCAG T G ST3GAL2 Ensembl:ENSG00000157350 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs28491205 Functional Loss SNV dbSNP153 33..33 33 - - - 36040 RMVar_ID_36040 Human_SNP_ID_607477599 A-to-I Human chr16 - 70436312 70436312 70436312 TTGGCCACCCCTTCCTGGGGTGACAGGAACCTAGGATTACAGGCATACGCCACGACACCCCGCTA TTGGCCACCCCTTCCTGGGGTGACAGGAACCTGGGATTACAGGCATACGCCACGACACCCCGCTA T C ST3GAL2 Ensembl:ENSG00000157350 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1333699257 Functional Loss SNV dbSNP153 33..33 33 - - - 36041 RMVar_ID_36041 Human_SNP_ID_607493359 A-to-I Human chr16 - 70485682 70485682 70485682 ACTCCGGAGGCTGAGGTGGGAGAGTCACTTGAACCCGGGAGACAGAGGTTGCAGTCAGCCAAGAT ACTCCGGAGGCTGAGGTGGGAGAGTCACTTGAGCCCGGGAGACAGAGGTTGCAGTCAGCCAAGAT T C COG4 Ensembl:ENSG00000103051 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs989134158 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81662,RMVar_hsa_circ_100295,RMVar_hsa_circ_122105,RMVar_hsa_circ_118209,RMVar_hsa_circ_95629,RMVar_hsa_circ_112041,RMVar_hsa_circ_179628,RMVar_hsa_circ_179630,RMVar_hsa_circ_179631,RMVar_hsa_circ_179629,RMVar_hsa_circ_179627,RMVar_hsa_circ_94808,RMVar_hsa_circ_179632,RMVar_hsa_circ_179633 36042 RMVar_ID_36042 Human_SNP_ID_607493841 A-to-I Human chr16 - 70487122 70487122 70487122 CATGCCCAGCTGATTTTTGTATTTTTAGTAGAAACGAGGTTTCACCATGCTGTCTAGGCTGGTCT CATGCCCAGCTGATTTTTGTATTTTTAGTAGAGACGAGGTTTCACCATGCTGTCTAGGCTGGTCT T C COG4 Ensembl:ENSG00000103051 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1391977770 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81662,RMVar_hsa_circ_100295,RMVar_hsa_circ_122105,RMVar_hsa_circ_118209,RMVar_hsa_circ_95629,RMVar_hsa_circ_112041,RMVar_hsa_circ_179628,RMVar_hsa_circ_179630,RMVar_hsa_circ_179631,RMVar_hsa_circ_179629,RMVar_hsa_circ_179627,RMVar_hsa_circ_94808,RMVar_hsa_circ_179632,RMVar_hsa_circ_179633 36043 RMVar_ID_36043 Human_SNP_ID_607493859 A-to-I Human chr16 - 70487183 70487183 70487183 CAACCTCTGCGATTCTCCTGCCTCAGCTTCCTAAGTTGCTGGGATTACAGGCACCTGACACCATG CAACCTCTGCGATTCTCCTGCCTCAGCTTCCTGAGTTGCTGGGATTACAGGCACCTGACACCATG T C COG4 Ensembl:ENSG00000103051 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs910187279 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81662,RMVar_hsa_circ_100295,RMVar_hsa_circ_122105,RMVar_hsa_circ_118209,RMVar_hsa_circ_95629,RMVar_hsa_circ_112041,RMVar_hsa_circ_179628,RMVar_hsa_circ_179630,RMVar_hsa_circ_179631,RMVar_hsa_circ_179629,RMVar_hsa_circ_179627,RMVar_hsa_circ_94808,RMVar_hsa_circ_179632,RMVar_hsa_circ_179633 36044 RMVar_ID_36044 Human_SNP_ID_607494141 A-to-I Human chr16 - 70488100 70488100 70488100 AAAATAATAGCCAGGTGTGGTGGCTCACACCTATAACCCCAGCACTTTGGGATGCCAAGGCGGGA AAAATAATAGCCAGGTGTGGTGGCTCACACCTGTAACCCCAGCACTTTGGGATGCCAAGGCGGGA T C COG4 Ensembl:ENSG00000103051 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1019050394 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81662,RMVar_hsa_circ_100295,RMVar_hsa_circ_122105,RMVar_hsa_circ_118209,RMVar_hsa_circ_95629,RMVar_hsa_circ_112041,RMVar_hsa_circ_179628,RMVar_hsa_circ_179630,RMVar_hsa_circ_179631,RMVar_hsa_circ_179629,RMVar_hsa_circ_179627,RMVar_hsa_circ_94808,RMVar_hsa_circ_179632,RMVar_hsa_circ_179633 36045 RMVar_ID_36045 Human_SNP_ID_607494142 A-to-I Human chr16 - 70488100 70488100 70488100 AAAATAATAGCCAGGTGTGGTGGCTCACACCTATAACCCCAGCACTTTGGGATGCCAAGGCGGGA AAAATAATAGCCAGGTGTGGTGGCTCACACCTCTAACCCCAGCACTTTGGGATGCCAAGGCGGGA T G COG4 Ensembl:ENSG00000103051 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1019050394 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81662,RMVar_hsa_circ_100295,RMVar_hsa_circ_122105,RMVar_hsa_circ_118209,RMVar_hsa_circ_95629,RMVar_hsa_circ_112041,RMVar_hsa_circ_179628,RMVar_hsa_circ_179630,RMVar_hsa_circ_179631,RMVar_hsa_circ_179629,RMVar_hsa_circ_179627,RMVar_hsa_circ_94808,RMVar_hsa_circ_179632,RMVar_hsa_circ_179633 36046 RMVar_ID_36046 Human_SNP_ID_607498718 A-to-I Human chr16 - 70504531 70504531 70504531 TCAATTTTGGCTCACTGCAATCTCCGCCTCCCAGGATCAAGCAGTTCTCGTGCCTCTGCCTCCTG TCAATTTTGGCTCACTGCAATCTCCGCCTCCCGGGATCAAGCAGTTCTCGTGCCTCTGCCTCCTG T C COG4 Ensembl:ENSG00000103051 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1380865126 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12797138 RMVar_hsa_circ_50,RMVar_hsa_circ_81662,RMVar_hsa_circ_100295,RMVar_hsa_circ_122105,RMVar_hsa_circ_118209,RMVar_hsa_circ_112041,RMVar_hsa_circ_179628,RMVar_hsa_circ_179630,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 36047 RMVar_ID_36047 Human_SNP_ID_607507068 A-to-I Human chr16 + 70531078 70531078 70531078 CATGAGGTCAGGAGATCGAGACCATTCTGGCTAACACAGTGAAACCCCATCTCTACTAAAAATAC CATGAGGTCAGGAGATCGAGACCATTCTGGCTGACACAGTGAAACCCCATCTCTACTAAAAATAC A G SF3B3 Ensembl:ENSG00000189091 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1332272859 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1107,RMVar_hsa_circ_121582,RMVar_hsa_circ_324347,RMVar_hsa_circ_338488,RMVar_hsa_circ_377675,RMVar_hsa_circ_179639,RMVar_hsa_circ_368211,RMVar_hsa_circ_330487,RMVar_hsa_circ_323717,RMVar_hsa_circ_306331,RMVar_hsa_circ_83258,RMVar_hsa_circ_287654,RMVar_hsa_circ_80173,RMVar_hsa_circ_119826,RMVar_hsa_circ_179641,RMVar_hsa_circ_179643,RMVar_hsa_circ_179644,RMVar_hsa_circ_179642,RMVar_hsa_circ_179640,RMVar_hsa_circ_46222,RMVar_hsa_circ_94251,RMVar_hsa_circ_179648,RMVar_hsa_circ_179649,RMVar_hsa_circ_318558,RMVar_hsa_circ_371365,RMVar_hsa_circ_101775,RMVar_hsa_circ_179651,RMVar_hsa_circ_179652,RMVar_hsa_circ_179650 36048 RMVar_ID_36048 Human_SNP_ID_607507204 A-to-I Human chr16 + 70531451 70531451 70531451 AGGTGCTGCCACAACGCCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACTATGTTGG AGGTGCTGCCACAACGCCCAGCTAATTTTTGTGTTTTTAGTAGAGATGGGGTTTCACTATGTTGG A G SF3B3 Ensembl:ENSG00000189091 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs552378221 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1107,RMVar_hsa_circ_121582,RMVar_hsa_circ_324347,RMVar_hsa_circ_338488,RMVar_hsa_circ_377675,RMVar_hsa_circ_179639,RMVar_hsa_circ_368211,RMVar_hsa_circ_330487,RMVar_hsa_circ_323717,RMVar_hsa_circ_306331,RMVar_hsa_circ_83258,RMVar_hsa_circ_287654,RMVar_hsa_circ_80173,RMVar_hsa_circ_119826,RMVar_hsa_circ_179641,RMVar_hsa_circ_179643,RMVar_hsa_circ_179644,RMVar_hsa_circ_179642,RMVar_hsa_circ_179640,RMVar_hsa_circ_46222,RMVar_hsa_circ_94251,RMVar_hsa_circ_179648,RMVar_hsa_circ_179649,RMVar_hsa_circ_318558,RMVar_hsa_circ_371365,RMVar_hsa_circ_101775,RMVar_hsa_circ_179651,RMVar_hsa_circ_179652,RMVar_hsa_circ_179650 36049 RMVar_ID_36049 Human_SNP_ID_607507209 A-to-I Human chr16 + 70531477 70531477 70531477 TTTTGTATTTTTAGTAGAGATGGGGTTTCACTATGTTGGCCAGGCTGGTCTTCTGACCCCAGGTG TTTTGTATTTTTAGTAGAGATGGGGTTTCACTGTGTTGGCCAGGCTGGTCTTCTGACCCCAGGTG A G SF3B3 Ensembl:ENSG00000189091 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1009173102 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17564279 RMVar_hsa_circ_1107,RMVar_hsa_circ_121582,RMVar_hsa_circ_324347,RMVar_hsa_circ_338488,RMVar_hsa_circ_377675,RMVar_hsa_circ_179639,RMVar_hsa_circ_368211,RMVar_hsa_circ_330487,RMVar_hsa_circ_323717,RMVar_hsa_circ_306331,RMVar_hsa_circ_83258,RMVar_hsa_circ_287654,RMVar_hsa_circ_80173,RMVar_hsa_circ_119826,RMVar_hsa_circ_179641,RMVar_hsa_circ_179643,RMVar_hsa_circ_179644,RMVar_hsa_circ_179642,RMVar_hsa_circ_179640,RMVar_hsa_circ_46222,RMVar_hsa_circ_94251,RMVar_hsa_circ_179648,RMVar_hsa_circ_179649,RMVar_hsa_circ_318558,RMVar_hsa_circ_371365,RMVar_hsa_circ_101775,RMVar_hsa_circ_179651,RMVar_hsa_circ_179652,RMVar_hsa_circ_179650 36050 RMVar_ID_36050 Human_SNP_ID_607509595 A-to-I Human chr16 + 70539959 70539959 70539959 TCACTATGCCCAGCTCATTTTGTACTTTTAGTAGAGACAGGGTTTCTCCATGTTAGTCAGGCTGG TCACTATGCCCAGCTCATTTTGTACTTTTAGTGGAGACAGGGTTTCTCCATGTTAGTCAGGCTGG A G SF3B3 Ensembl:ENSG00000189091 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs921288947 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35580,RMVar_hsa_circ_1107,RMVar_hsa_circ_121582,RMVar_hsa_circ_324347,RMVar_hsa_circ_179639,RMVar_hsa_circ_368211,RMVar_hsa_circ_330487,RMVar_hsa_circ_83258,RMVar_hsa_circ_287654,RMVar_hsa_circ_80173,RMVar_hsa_circ_179641,RMVar_hsa_circ_179643,RMVar_hsa_circ_179642,RMVar_hsa_circ_179640,RMVar_hsa_circ_46222,RMVar_hsa_circ_94251,RMVar_hsa_circ_179649,RMVar_hsa_circ_101775,RMVar_hsa_circ_118412,RMVar_hsa_circ_308069,RMVar_hsa_circ_376283,RMVar_hsa_circ_179650,RMVar_hsa_circ_276082,RMVar_hsa_circ_80721,RMVar_hsa_circ_90869,RMVar_hsa_circ_46268,RMVar_hsa_circ_56989,RMVar_hsa_circ_102025,RMVar_hsa_circ_179655,RMVar_hsa_circ_179657,RMVar_hsa_circ_179658,RMVar_hsa_circ_179656,RMVar_hsa_circ_179653,RMVar_hsa_circ_179654,RMVar_hsa_circ_86802,RMVar_hsa_circ_179662,RMVar_hsa_circ_179663,RMVar_hsa_circ_282589,RMVar_hsa_circ_375363,RMVar_hsa_circ_378115,RMVar_hsa_circ_378757,RMVar_hsa_circ_364283,RMVar_hsa_circ_277893,RMVar_hsa_circ_58019,RMVar_hsa_circ_104089,RMVar_hsa_circ_179665,RMVar_hsa_circ_47365,RMVar_hsa_circ_179666 36051 RMVar_ID_36051 Human_SNP_ID_607509688 A-to-I Human chr16 + 70540270 70540246 70540270 TACAAAATGAGCTGGTCTCAAACCAGCTGGCCAAGCTGGTCTCAAACTCCTGACCTCAAGTGATC TACAAAATG________________________AGCTGGTCTCAAACTCCTGACCTCAAGTGATC GAGCTGGTCTCAAACCAGCTGGCCA G SF3B3 Ensembl:ENSG00000189091 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006596027 Functional Loss DEL dbSNP153 10..33 33 - - - RMVar_hsa_circ_35580,RMVar_hsa_circ_1107,RMVar_hsa_circ_121582,RMVar_hsa_circ_324347,RMVar_hsa_circ_179639,RMVar_hsa_circ_368211,RMVar_hsa_circ_330487,RMVar_hsa_circ_83258,RMVar_hsa_circ_287654,RMVar_hsa_circ_80173,RMVar_hsa_circ_179641,RMVar_hsa_circ_179643,RMVar_hsa_circ_179642,RMVar_hsa_circ_179640,RMVar_hsa_circ_46222,RMVar_hsa_circ_94251,RMVar_hsa_circ_179649,RMVar_hsa_circ_101775,RMVar_hsa_circ_118412,RMVar_hsa_circ_308069,RMVar_hsa_circ_376283,RMVar_hsa_circ_179650,RMVar_hsa_circ_276082,RMVar_hsa_circ_80721,RMVar_hsa_circ_90869,RMVar_hsa_circ_46268,RMVar_hsa_circ_56989,RMVar_hsa_circ_102025,RMVar_hsa_circ_179655,RMVar_hsa_circ_179657,RMVar_hsa_circ_179658,RMVar_hsa_circ_179656,RMVar_hsa_circ_179653,RMVar_hsa_circ_179654,RMVar_hsa_circ_86802,RMVar_hsa_circ_179662,RMVar_hsa_circ_179663,RMVar_hsa_circ_282589,RMVar_hsa_circ_375363,RMVar_hsa_circ_378115,RMVar_hsa_circ_378757,RMVar_hsa_circ_364283,RMVar_hsa_circ_277893,RMVar_hsa_circ_58019,RMVar_hsa_circ_104089,RMVar_hsa_circ_179665,RMVar_hsa_circ_47365,RMVar_hsa_circ_179666 36052 RMVar_ID_36052 Human_SNP_ID_607510395 A-to-I Human chr16 + 70542887 70542887 70542887 GGGACTACAAGCGCCCGCCACCATGCCCAGCTAATTTTTTGTATTTTTAGTAGAGACAGGGTTTC GGGACTACAAGCGCCCGCCACCATGCCCAGCTGATTTTTTGTATTTTTAGTAGAGACAGGGTTTC A G SF3B3 Ensembl:ENSG00000189091 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs962156717 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35580,RMVar_hsa_circ_1107,RMVar_hsa_circ_121582,RMVar_hsa_circ_179639,RMVar_hsa_circ_368211,RMVar_hsa_circ_330487,RMVar_hsa_circ_83258,RMVar_hsa_circ_287654,RMVar_hsa_circ_80173,RMVar_hsa_circ_179641,RMVar_hsa_circ_179643,RMVar_hsa_circ_179642,RMVar_hsa_circ_179640,RMVar_hsa_circ_46222,RMVar_hsa_circ_101775,RMVar_hsa_circ_118412,RMVar_hsa_circ_376283,RMVar_hsa_circ_179650,RMVar_hsa_circ_276082,RMVar_hsa_circ_80721,RMVar_hsa_circ_90869,RMVar_hsa_circ_46268,RMVar_hsa_circ_179667,RMVar_hsa_circ_56989,RMVar_hsa_circ_102025,RMVar_hsa_circ_179655,RMVar_hsa_circ_179657,RMVar_hsa_circ_179656,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_378115,RMVar_hsa_circ_378757,RMVar_hsa_circ_364283,RMVar_hsa_circ_277893,RMVar_hsa_circ_58019,RMVar_hsa_circ_65184,RMVar_hsa_circ_119000,RMVar_hsa_circ_104089,RMVar_hsa_circ_179665,RMVar_hsa_circ_47365,RMVar_hsa_circ_297241,RMVar_hsa_circ_179666,RMVar_hsa_circ_338483,RMVar_hsa_circ_278842,RMVar_hsa_circ_111280,RMVar_hsa_circ_115266,RMVar_hsa_circ_99528,RMVar_hsa_circ_179669,RMVar_hsa_circ_179671,RMVar_hsa_circ_179672,RMVar_hsa_circ_179673,RMVar_hsa_circ_179670,RMVar_hsa_circ_179668 36053 RMVar_ID_36053 Human_SNP_ID_607510396 A-to-I Human chr16 + 70542887 70542887 70542887 GGGACTACAAGCGCCCGCCACCATGCCCAGCTAATTTTTTGTATTTTTAGTAGAGACAGGGTTTC GGGACTACAAGCGCCCGCCACCATGCCCAGCTTATTTTTTGTATTTTTAGTAGAGACAGGGTTTC A T SF3B3 Ensembl:ENSG00000189091 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs962156717 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35580,RMVar_hsa_circ_1107,RMVar_hsa_circ_121582,RMVar_hsa_circ_179639,RMVar_hsa_circ_368211,RMVar_hsa_circ_330487,RMVar_hsa_circ_83258,RMVar_hsa_circ_287654,RMVar_hsa_circ_80173,RMVar_hsa_circ_179641,RMVar_hsa_circ_179643,RMVar_hsa_circ_179642,RMVar_hsa_circ_179640,RMVar_hsa_circ_46222,RMVar_hsa_circ_101775,RMVar_hsa_circ_118412,RMVar_hsa_circ_376283,RMVar_hsa_circ_179650,RMVar_hsa_circ_276082,RMVar_hsa_circ_80721,RMVar_hsa_circ_90869,RMVar_hsa_circ_46268,RMVar_hsa_circ_179667,RMVar_hsa_circ_56989,RMVar_hsa_circ_102025,RMVar_hsa_circ_179655,RMVar_hsa_circ_179657,RMVar_hsa_circ_179656,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_378115,RMVar_hsa_circ_378757,RMVar_hsa_circ_364283,RMVar_hsa_circ_277893,RMVar_hsa_circ_58019,RMVar_hsa_circ_65184,RMVar_hsa_circ_119000,RMVar_hsa_circ_104089,RMVar_hsa_circ_179665,RMVar_hsa_circ_47365,RMVar_hsa_circ_297241,RMVar_hsa_circ_179666,RMVar_hsa_circ_338483,RMVar_hsa_circ_278842,RMVar_hsa_circ_111280,RMVar_hsa_circ_115266,RMVar_hsa_circ_99528,RMVar_hsa_circ_179669,RMVar_hsa_circ_179671,RMVar_hsa_circ_179672,RMVar_hsa_circ_179673,RMVar_hsa_circ_179670,RMVar_hsa_circ_179668 36054 RMVar_ID_36054 Human_SNP_ID_607510397 A-to-I Human chr16 + 70542897 70542897 70542897 GCGCCCGCCACCATGCCCAGCTAATTTTTTGTATTTTTAGTAGAGACAGGGTTTCACTGTTAACT GCGCCCGCCACCATGCCCAGCTAATTTTTTGTGTTTTTAGTAGAGACAGGGTTTCACTGTTAACT A G SF3B3 Ensembl:ENSG00000189091 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs868700300 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35580,RMVar_hsa_circ_1107,RMVar_hsa_circ_121582,RMVar_hsa_circ_179639,RMVar_hsa_circ_368211,RMVar_hsa_circ_330487,RMVar_hsa_circ_83258,RMVar_hsa_circ_287654,RMVar_hsa_circ_80173,RMVar_hsa_circ_179641,RMVar_hsa_circ_179643,RMVar_hsa_circ_179642,RMVar_hsa_circ_179640,RMVar_hsa_circ_46222,RMVar_hsa_circ_101775,RMVar_hsa_circ_118412,RMVar_hsa_circ_376283,RMVar_hsa_circ_179650,RMVar_hsa_circ_276082,RMVar_hsa_circ_80721,RMVar_hsa_circ_90869,RMVar_hsa_circ_46268,RMVar_hsa_circ_179667,RMVar_hsa_circ_56989,RMVar_hsa_circ_102025,RMVar_hsa_circ_179655,RMVar_hsa_circ_179657,RMVar_hsa_circ_179656,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_378115,RMVar_hsa_circ_378757,RMVar_hsa_circ_364283,RMVar_hsa_circ_277893,RMVar_hsa_circ_58019,RMVar_hsa_circ_65184,RMVar_hsa_circ_119000,RMVar_hsa_circ_104089,RMVar_hsa_circ_179665,RMVar_hsa_circ_47365,RMVar_hsa_circ_297241,RMVar_hsa_circ_179666,RMVar_hsa_circ_338483,RMVar_hsa_circ_278842,RMVar_hsa_circ_111280,RMVar_hsa_circ_115266,RMVar_hsa_circ_99528,RMVar_hsa_circ_179669,RMVar_hsa_circ_179671,RMVar_hsa_circ_179672,RMVar_hsa_circ_179673,RMVar_hsa_circ_179670,RMVar_hsa_circ_179668 36055 RMVar_ID_36055 Human_SNP_ID_607510496 A-to-I Human chr16 + 70543263 70543263 70543263 AACCCTGTCTCTACTAAAAGAAATACAAAATTAGCCAGGCATGGTGGCGCATGCCTGTAATCGCA AACCCTGTCTCTACTAAAAGAAATACAAAATTGGCCAGGCATGGTGGCGCATGCCTGTAATCGCA A G SF3B3 Ensembl:ENSG00000189091 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1313838237 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35580,RMVar_hsa_circ_1107,RMVar_hsa_circ_121582,RMVar_hsa_circ_179639,RMVar_hsa_circ_368211,RMVar_hsa_circ_330487,RMVar_hsa_circ_83258,RMVar_hsa_circ_287654,RMVar_hsa_circ_80173,RMVar_hsa_circ_179641,RMVar_hsa_circ_179643,RMVar_hsa_circ_179642,RMVar_hsa_circ_179640,RMVar_hsa_circ_46222,RMVar_hsa_circ_101775,RMVar_hsa_circ_118412,RMVar_hsa_circ_376283,RMVar_hsa_circ_179650,RMVar_hsa_circ_276082,RMVar_hsa_circ_80721,RMVar_hsa_circ_90869,RMVar_hsa_circ_46268,RMVar_hsa_circ_179667,RMVar_hsa_circ_56989,RMVar_hsa_circ_102025,RMVar_hsa_circ_179655,RMVar_hsa_circ_179657,RMVar_hsa_circ_179656,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_378115,RMVar_hsa_circ_378757,RMVar_hsa_circ_364283,RMVar_hsa_circ_277893,RMVar_hsa_circ_58019,RMVar_hsa_circ_65184,RMVar_hsa_circ_119000,RMVar_hsa_circ_104089,RMVar_hsa_circ_179665,RMVar_hsa_circ_47365,RMVar_hsa_circ_297241,RMVar_hsa_circ_179666,RMVar_hsa_circ_338483,RMVar_hsa_circ_278842,RMVar_hsa_circ_111280,RMVar_hsa_circ_115266,RMVar_hsa_circ_99528,RMVar_hsa_circ_179669,RMVar_hsa_circ_179671,RMVar_hsa_circ_179672,RMVar_hsa_circ_179673,RMVar_hsa_circ_179670,RMVar_hsa_circ_179668 36056 RMVar_ID_36056 Human_SNP_ID_607510709 A-to-I Human chr16 + 70543885 70543885 70543885 TTTTTTTAATTTTTTTTTGAGACAAGAGTCTCACTCTGTTACCCAGGCTAGAGTGCAGTGGCACA TTTTTTTAATTTTTTTTTGAGACAAGAGTCTCCCTCTGTTACCCAGGCTAGAGTGCAGTGGCACA A C SF3B3 Ensembl:ENSG00000189091 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs918843425 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17564280 RMVar_hsa_circ_35580,RMVar_hsa_circ_1107,RMVar_hsa_circ_121582,RMVar_hsa_circ_179639,RMVar_hsa_circ_368211,RMVar_hsa_circ_330487,RMVar_hsa_circ_83258,RMVar_hsa_circ_287654,RMVar_hsa_circ_80173,RMVar_hsa_circ_179641,RMVar_hsa_circ_179643,RMVar_hsa_circ_179642,RMVar_hsa_circ_179640,RMVar_hsa_circ_46222,RMVar_hsa_circ_101775,RMVar_hsa_circ_118412,RMVar_hsa_circ_376283,RMVar_hsa_circ_179650,RMVar_hsa_circ_276082,RMVar_hsa_circ_80721,RMVar_hsa_circ_90869,RMVar_hsa_circ_46268,RMVar_hsa_circ_179667,RMVar_hsa_circ_56989,RMVar_hsa_circ_102025,RMVar_hsa_circ_179655,RMVar_hsa_circ_179657,RMVar_hsa_circ_179656,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_378115,RMVar_hsa_circ_378757,RMVar_hsa_circ_364283,RMVar_hsa_circ_277893,RMVar_hsa_circ_58019,RMVar_hsa_circ_65184,RMVar_hsa_circ_119000,RMVar_hsa_circ_104089,RMVar_hsa_circ_179665,RMVar_hsa_circ_47365,RMVar_hsa_circ_297241,RMVar_hsa_circ_179666,RMVar_hsa_circ_338483,RMVar_hsa_circ_278842,RMVar_hsa_circ_111280,RMVar_hsa_circ_115266,RMVar_hsa_circ_99528,RMVar_hsa_circ_179669,RMVar_hsa_circ_179671,RMVar_hsa_circ_179672,RMVar_hsa_circ_179673,RMVar_hsa_circ_179670,RMVar_hsa_circ_179668 36057 RMVar_ID_36057 Human_SNP_ID_607511337 A-to-I Human chr16 + 70546084 70546084 70546084 GCCCAGTCTCAAGCAAGCAATTCTCCCACCTTAGCTTCTGGAGTAGCTGGGACTACAGGTGTGCG GCCCAGTCTCAAGCAAGCAATTCTCCCACCTTGGCTTCTGGAGTAGCTGGGACTACAGGTGTGCG A G SF3B3 Ensembl:ENSG00000189091 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs893683674 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35580,RMVar_hsa_circ_1107,RMVar_hsa_circ_121582,RMVar_hsa_circ_179639,RMVar_hsa_circ_368211,RMVar_hsa_circ_330487,RMVar_hsa_circ_83258,RMVar_hsa_circ_80173,RMVar_hsa_circ_179641,RMVar_hsa_circ_179642,RMVar_hsa_circ_179640,RMVar_hsa_circ_46222,RMVar_hsa_circ_101775,RMVar_hsa_circ_118412,RMVar_hsa_circ_376283,RMVar_hsa_circ_179650,RMVar_hsa_circ_80721,RMVar_hsa_circ_90869,RMVar_hsa_circ_46268,RMVar_hsa_circ_179667,RMVar_hsa_circ_56989,RMVar_hsa_circ_102025,RMVar_hsa_circ_179655,RMVar_hsa_circ_179656,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_378115,RMVar_hsa_circ_378757,RMVar_hsa_circ_364283,RMVar_hsa_circ_58019,RMVar_hsa_circ_65184,RMVar_hsa_circ_119000,RMVar_hsa_circ_104089,RMVar_hsa_circ_179665,RMVar_hsa_circ_47365,RMVar_hsa_circ_179666,RMVar_hsa_circ_338483,RMVar_hsa_circ_278842,RMVar_hsa_circ_111280,RMVar_hsa_circ_115266,RMVar_hsa_circ_99528,RMVar_hsa_circ_179669,RMVar_hsa_circ_179671,RMVar_hsa_circ_179672,RMVar_hsa_circ_179670,RMVar_hsa_circ_179668,RMVar_hsa_circ_95163,RMVar_hsa_circ_110498,RMVar_hsa_circ_352474,RMVar_hsa_circ_374189,RMVar_hsa_circ_123867,RMVar_hsa_circ_179675,RMVar_hsa_circ_78168,RMVar_hsa_circ_89946,RMVar_hsa_circ_179677,RMVar_hsa_circ_179679,RMVar_hsa_circ_179680,RMVar_hsa_circ_179678,RMVar_hsa_circ_179676 36058 RMVar_ID_36058 Human_SNP_ID_607513164 A-to-I Human chr16 + 70553046 70553046 70553046 AATTCTGCTCAGCCTCCCGAGTAGTTGGAATTACAGGCGCCCACCACCACACCCAGCTAATTTTT AATTCTGCTCAGCCTCCCGAGTAGTTGGAATTGCAGGCGCCCACCACCACACCCAGCTAATTTTT A G SF3B3 Ensembl:ENSG00000189091 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027298469 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35580,RMVar_hsa_circ_1107,RMVar_hsa_circ_121582,RMVar_hsa_circ_179639,RMVar_hsa_circ_368211,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_46268,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_378115,RMVar_hsa_circ_378757,RMVar_hsa_circ_364283,RMVar_hsa_circ_58019,RMVar_hsa_circ_65184,RMVar_hsa_circ_119000,RMVar_hsa_circ_179665,RMVar_hsa_circ_47365,RMVar_hsa_circ_338483,RMVar_hsa_circ_111280,RMVar_hsa_circ_115266,RMVar_hsa_circ_99528,RMVar_hsa_circ_179669,RMVar_hsa_circ_179671,RMVar_hsa_circ_179670,RMVar_hsa_circ_179668,RMVar_hsa_circ_95163,RMVar_hsa_circ_110498,RMVar_hsa_circ_352474,RMVar_hsa_circ_374189,RMVar_hsa_circ_123867,RMVar_hsa_circ_89946,RMVar_hsa_circ_179677,RMVar_hsa_circ_179679,RMVar_hsa_circ_179680,RMVar_hsa_circ_179678,RMVar_hsa_circ_179676,RMVar_hsa_circ_124155,RMVar_hsa_circ_340678,RMVar_hsa_circ_333063,RMVar_hsa_circ_94340,RMVar_hsa_circ_24064,RMVar_hsa_circ_66049,RMVar_hsa_circ_24318,RMVar_hsa_circ_179682,RMVar_hsa_circ_179683,RMVar_hsa_circ_179681 36059 RMVar_ID_36059 Human_SNP_ID_607519245 A-to-I Human chr16 + 70575247 70575247 70575247 TTGAGATGAAGTCTTACTCTGTTGCCCAGGCTAGAGTACAGAGGCACAATCTCGGCTCACCACAG TTGAGATGAAGTCTTACTCTGTTGCCCAGGCTGGAGTACAGAGGCACAATCTCGGCTCACCACAG A G SF3B3 Ensembl:ENSG00000189091 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1200413562 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12799356 RMVar_hsa_circ_121582,RMVar_hsa_circ_179639,RMVar_hsa_circ_83258,RMVar_hsa_circ_179640,RMVar_hsa_circ_86802,RMVar_hsa_circ_179663,RMVar_hsa_circ_123867,RMVar_hsa_circ_179680,RMVar_hsa_circ_94340,RMVar_hsa_circ_179681,RMVar_hsa_circ_103993,RMVar_hsa_circ_124047,RMVar_hsa_circ_179702,RMVar_hsa_circ_179703 36060 RMVar_ID_36060 Human_SNP_ID_607519717 A-to-I Human chr16 + 70576866 70576864 70576866 AGACTGATTTACTGGGCCTGGCATGGTGGCTCACACCTGTAATCCCAGCACTTTGAGAGGCTGAG AGACTGATTTACTGGGCCTGGCATGGTGGCT__CACCTGTAATCCCAGCACTTTGAGAGGCTGAG TCA T SF3B3 Ensembl:ENSG00000189091 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1453706677 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_478911 RMVar_hsa_circ_121582,RMVar_hsa_circ_179639,RMVar_hsa_circ_83258,RMVar_hsa_circ_179640,RMVar_hsa_circ_86802,RMVar_hsa_circ_179663,RMVar_hsa_circ_123867,RMVar_hsa_circ_179680,RMVar_hsa_circ_94340,RMVar_hsa_circ_179681,RMVar_hsa_circ_103993,RMVar_hsa_circ_124047,RMVar_hsa_circ_179702,RMVar_hsa_circ_179703 36061 RMVar_ID_36061 Human_SNP_ID_607519762 A-to-I Human chr16 + 70577091 70577091 70577091 TTGAGGCTGCAGTGAGCTGTGATTGCGCCACTACACTCCAGCCTGGATGACAGGACGAAACCTGT TTGAGGCTGCAGTGAGCTGTGATTGCGCCACTGCACTCCAGCCTGGATGACAGGACGAAACCTGT A G SF3B3 Ensembl:ENSG00000189091 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1454225426 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6532938,Human_RBP_ID_12799442 RMVar_hsa_circ_121582,RMVar_hsa_circ_179639,RMVar_hsa_circ_83258,RMVar_hsa_circ_179640,RMVar_hsa_circ_86802,RMVar_hsa_circ_179663,RMVar_hsa_circ_123867,RMVar_hsa_circ_179680,RMVar_hsa_circ_94340,RMVar_hsa_circ_179681,RMVar_hsa_circ_103993,RMVar_hsa_circ_124047,RMVar_hsa_circ_179702,RMVar_hsa_circ_179703 36062 RMVar_ID_36062 Human_SNP_ID_607526733 A-to-I Human chr16 + 70603546 70603545 70603546 GTGATCCACCCGCCTCAGCCTCCCAGAGTGCTAGGGTTACAGGTGTGAGTCACCGTGCCCGGCCT GTGATCCACCCGCCTCAGCCTCCCAGAGTGCT_GGGTTACAGGTGTGAGTCACCGTGCCCGGCCT TA T IL34 Ensembl:ENSG00000157368 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs763206905 Functional Loss DEL dbSNP153 33..33 33 - - - 36063 RMVar_ID_36063 Human_SNP_ID_607794838 A-to-I Human chr16 + 71635066 71635066 71635066 AAGCAAAAAAATGGCCGGCCTCGGCGGCTCACACCTGTAACCCCAGCACTTTGGGAGGCTGAGGT AAGCAAAAAAATGGCCGGCCTCGGCGGCTCACGCCTGTAACCCCAGCACTTTGGGAGGCTGAGGT A G MARVELD3 Ensembl:ENSG00000140832 Protein coding intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs921104219 Functional Loss SNV dbSNP153 33..33 33 - - - 36064 RMVar_ID_36064 Human_SNP_ID_607806410 A-to-I Human chr16 - 71676928 71676928 71676928 CCTGGCCAACATGGTGAAACCCCAGCTCTACTAAAAATACAAAAAATTAGCCTGGCATGGTGGGG CCTGGCCAACATGGTGAAACCCCAGCTCTACTGAAAATACAAAAAATTAGCCTGGCATGGTGGGG T C PHLPP2 Ensembl:ENSG00000040199 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1486203606 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_312669,RMVar_hsa_circ_20484,RMVar_hsa_circ_179759,RMVar_hsa_circ_295768,RMVar_hsa_circ_316451,RMVar_hsa_circ_358023,RMVar_hsa_circ_359210,RMVar_hsa_circ_378879,RMVar_hsa_circ_267074,RMVar_hsa_circ_69085,RMVar_hsa_circ_45982,RMVar_hsa_circ_179769,RMVar_hsa_circ_268729,RMVar_hsa_circ_284458,RMVar_hsa_circ_336672,RMVar_hsa_circ_14005,RMVar_hsa_circ_91472,RMVar_hsa_circ_297120,RMVar_hsa_circ_179771,RMVar_hsa_circ_319403,RMVar_hsa_circ_179775,RMVar_hsa_circ_179776,RMVar_hsa_circ_293916,RMVar_hsa_circ_123475,RMVar_hsa_circ_179778,RMVar_hsa_circ_179779,RMVar_hsa_circ_303946,RMVar_hsa_circ_88313,RMVar_hsa_circ_179780,RMVar_hsa_circ_179782,RMVar_hsa_circ_6161,RMVar_hsa_circ_179781,RMVar_hsa_circ_283009,RMVar_hsa_circ_290439,RMVar_hsa_circ_292948,RMVar_hsa_circ_298899,RMVar_hsa_circ_289821,RMVar_hsa_circ_49787,RMVar_hsa_circ_179785,RMVar_hsa_circ_179787,RMVar_hsa_circ_179788,RMVar_hsa_circ_179786,RMVar_hsa_circ_179784 36065 RMVar_ID_36065 Human_SNP_ID_607808341 A-to-I Human chr16 - 71683867 71683867 71683867 AGAATCGCTTGAACCCAGGAGGCGGAGATTGCAGTGAGCCAAGATCATTCCATTGCACTCCAGCC AGAATCGCTTGAACCCAGGAGGCGGAGATTGCTGTGAGCCAAGATCATTCCATTGCACTCCAGCC T A PHLPP2 Ensembl:ENSG00000040199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs921169633 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_358023,RMVar_hsa_circ_359210,RMVar_hsa_circ_378879,RMVar_hsa_circ_69085,RMVar_hsa_circ_14005,RMVar_hsa_circ_91472,RMVar_hsa_circ_319403,RMVar_hsa_circ_179776,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_289821,RMVar_hsa_circ_49787,RMVar_hsa_circ_179787,RMVar_hsa_circ_179788,RMVar_hsa_circ_179786,RMVar_hsa_circ_347399,RMVar_hsa_circ_90415,RMVar_hsa_circ_179790,RMVar_hsa_circ_337735,RMVar_hsa_circ_372980,RMVar_hsa_circ_179793 36066 RMVar_ID_36066 Human_SNP_ID_607808346 A-to-I Human chr16 - 71683883 71683883 71683883 GATGCTGAGCTGCAGGAGAATCGCTTGAACCCAGGAGGCGGAGATTGCAGTGAGCCAAGATCATT GATGCTGAGCTGCAGGAGAATCGCTTGAACCCGGGAGGCGGAGATTGCAGTGAGCCAAGATCATT T C PHLPP2 Ensembl:ENSG00000040199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991447915 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_358023,RMVar_hsa_circ_359210,RMVar_hsa_circ_378879,RMVar_hsa_circ_69085,RMVar_hsa_circ_14005,RMVar_hsa_circ_91472,RMVar_hsa_circ_319403,RMVar_hsa_circ_179776,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_289821,RMVar_hsa_circ_49787,RMVar_hsa_circ_179787,RMVar_hsa_circ_179788,RMVar_hsa_circ_179786,RMVar_hsa_circ_347399,RMVar_hsa_circ_90415,RMVar_hsa_circ_179790,RMVar_hsa_circ_337735,RMVar_hsa_circ_372980,RMVar_hsa_circ_179793 36067 RMVar_ID_36067 Human_SNP_ID_607818654 A-to-I Human chr16 - 71720630 71720630 71720630 GAAGTCCTGGCCTCAGGTGATCCGCCTGCCTCAGCCTGCCAAAGTGCTGGGATTACAGGCATGAG GAAGTCCTGGCCTCAGGTGATCCGCCTGCCTCGGCCTGCCAAAGTGCTGGGATTACAGGCATGAG T C PHLPP2 Ensembl:ENSG00000040199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1265901161 Functional Loss SNV dbSNP153 33..33 33 - - - 36068 RMVar_ID_36068 Human_SNP_ID_607818677 A-to-I Human chr16 - 71720682 71720682 71720682 TTTTGTATTTTTAGTAGAGACAGGGTTTCTCTATGTTGGTCAGGCTGGTGTTGAAGTCCTGGCCT TTTTGTATTTTTAGTAGAGACAGGGTTTCTCTGTGTTGGTCAGGCTGGTGTTGAAGTCCTGGCCT T C PHLPP2 Ensembl:ENSG00000040199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs897219119 Functional Loss SNV dbSNP153 33..33 33 - - - 36069 RMVar_ID_36069 Human_SNP_ID_607819105 A-to-I Human chr16 - 71722249 71722249 71722249 TTTTGTATTTTTAGTAGAGACAGGGTTGCGCTATGTTTCCCAGGCTGGTCTTGAACTCCTGATCT TTTTGTATTTTTAGTAGAGACAGGGTTGCGCTGTGTTTCCCAGGCTGGTCTTGAACTCCTGATCT T C PHLPP2 Ensembl:ENSG00000040199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs770540478 Functional Loss SNV dbSNP153 33..33 33 - - - 36070 RMVar_ID_36070 Human_SNP_ID_607819134 A-to-I Human chr16 - 71722318 71722318 71722318 GCGATTCTCCTGCCTCAGCCTCTTGAGTAGCTAGGATCACGGGCACCCGCCACCACACCCCACTG GCGATTCTCCTGCCTCAGCCTCTTGAGTAGCTGGGATCACGGGCACCCGCCACCACACCCCACTG T C PHLPP2 Ensembl:ENSG00000040199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs532311585 Functional Loss SNV dbSNP153 33..33 33 - - - 36071 RMVar_ID_36071 Human_SNP_ID_607819161 A-to-I Human chr16 - 71722421 71722421 71722421 AGTTTTTTTTCTTTTTATTTATTTTTTGAGACAGGGTCTCACTCTGTCACCCAAGCCTGAGTGCA AGTTTTTTTTCTTTTTATTTATTTTTTGAGACGGGGTCTCACTCTGTCACCCAAGCCTGAGTGCA T C PHLPP2 Ensembl:ENSG00000040199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs760467857 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6533654,Human_RBP_ID_12801655 36072 RMVar_ID_36072 Human_SNP_ID_607821292 A-to-I Human chr16 - 71730253 71730253 71730253 ATTAATTCATCTAAGTAATCTCAAAAAACTGTAGGAAGGGTGCTCTCCCTGAGAAGCTTCTCCCA ATTAATTCATCTAAGTAATCTCAAAAAACTGTGGGAAGGGTGCTCTCCCTGAGAAGCTTCTCCCA T C AP1G1 Ensembl:ENSG00000166747 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1319596636 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_479021,Human_RBP_ID_4381999,Human_RBP_ID_6533694,Human_RBP_ID_8809996,Human_RBP_ID_17370702,Human_RBP_ID_17487612,Human_RBP_ID_18287222,Human_RBP_ID_26810542 Human_miRNA_ID_275651,Human_miRNA_ID_1189122,Human_miRNA_ID_1802191,Human_miRNA_ID_2054125,Human_miRNA_ID_2922839 RMVar_hsa_circ_122896,RMVar_hsa_circ_179800 36073 RMVar_ID_36073 Human_SNP_ID_607827238 A-to-I Human chr16 - 71751117 71751117 71751117 GGAGTCTCAGTCTGTTGCTCAGGCTGGAGTGCAGTGGCGCAAACTCGGCTCACTGCAAGCTCGGC GGAGTCTCAGTCTGTTGCTCAGGCTGGAGTGCGGTGGCGCAAACTCGGCTCACTGCAAGCTCGGC T C AP1G1 Ensembl:ENSG00000166747 Protein coding intron GSE107867 ASD brains,cerebellum;ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs913746288 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6993,RMVar_hsa_circ_119209,RMVar_hsa_circ_122896,RMVar_hsa_circ_179800,RMVar_hsa_circ_77600,RMVar_hsa_circ_100728,RMVar_hsa_circ_59826,RMVar_hsa_circ_115682,RMVar_hsa_circ_36220,RMVar_hsa_circ_179802,RMVar_hsa_circ_179803,RMVar_hsa_circ_179801,RMVar_hsa_circ_46391,RMVar_hsa_circ_34236,RMVar_hsa_circ_179808,RMVar_hsa_circ_86449,RMVar_hsa_circ_179809,RMVar_hsa_circ_348437,RMVar_hsa_circ_353710,RMVar_hsa_circ_356337,RMVar_hsa_circ_91209,RMVar_hsa_circ_60469,RMVar_hsa_circ_7819,RMVar_hsa_circ_179814,RMVar_hsa_circ_179815,RMVar_hsa_circ_72474,RMVar_hsa_circ_98656,RMVar_hsa_circ_179816,RMVar_hsa_circ_346260,RMVar_hsa_circ_280182,RMVar_hsa_circ_7417,RMVar_hsa_circ_52724,RMVar_hsa_circ_36173,RMVar_hsa_circ_304744,RMVar_hsa_circ_315328,RMVar_hsa_circ_179820,RMVar_hsa_circ_179821 36074 RMVar_ID_36074 Human_SNP_ID_607828376 A-to-I Human chr16 - 71755243 71755243 71755243 TTTTTTTCTTTTTGTAGAGATGGGGTTTCGCTATGTTGTCCAGGCTGGTCTCGAACTCCTGGACT TTTTTTTCTTTTTGTAGAGATGGGGTTTCGCTGTGTTGTCCAGGCTGGTCTCGAACTCCTGGACT T C AP1G1 Ensembl:ENSG00000166747 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs537338461 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12802156 RMVar_hsa_circ_6993,RMVar_hsa_circ_122896,RMVar_hsa_circ_179800,RMVar_hsa_circ_77600,RMVar_hsa_circ_100728,RMVar_hsa_circ_59826,RMVar_hsa_circ_115682,RMVar_hsa_circ_36220,RMVar_hsa_circ_179802,RMVar_hsa_circ_179803,RMVar_hsa_circ_46391,RMVar_hsa_circ_34236,RMVar_hsa_circ_179808,RMVar_hsa_circ_86449,RMVar_hsa_circ_179809,RMVar_hsa_circ_348437,RMVar_hsa_circ_353710,RMVar_hsa_circ_91209,RMVar_hsa_circ_60469,RMVar_hsa_circ_7819,RMVar_hsa_circ_179815,RMVar_hsa_circ_72474,RMVar_hsa_circ_98656,RMVar_hsa_circ_179816,RMVar_hsa_circ_346260,RMVar_hsa_circ_7417,RMVar_hsa_circ_52724,RMVar_hsa_circ_36173,RMVar_hsa_circ_315328,RMVar_hsa_circ_99935,RMVar_hsa_circ_179821,RMVar_hsa_circ_102424,RMVar_hsa_circ_179823,RMVar_hsa_circ_23773,RMVar_hsa_circ_179822 36075 RMVar_ID_36075 Human_SNP_ID_607835612 A-to-I Human chr16 - 71779479 71779479 71779479 AAAATTAGCTGGGGTTGGTGGCACGCATCTGTAGTTCCAGCTACTTGGGAGGTTGAGGCACGAGA AAAATTAGCTGGGGTTGGTGGCACGCATCTGTGGTTCCAGCTACTTGGGAGGTTGAGGCACGAGA T C AP1G1 Ensembl:ENSG00000166747 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1423103048 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7819,RMVar_hsa_circ_98656,RMVar_hsa_circ_179816,RMVar_hsa_circ_99935,RMVar_hsa_circ_179823,RMVar_hsa_circ_21890,RMVar_hsa_circ_304228,RMVar_hsa_circ_179830,RMVar_hsa_circ_120305,RMVar_hsa_circ_338826,RMVar_hsa_circ_179835,RMVar_hsa_circ_179834,RMVar_hsa_circ_375593,RMVar_hsa_circ_179845,RMVar_hsa_circ_179846,RMVar_hsa_circ_295328 36076 RMVar_ID_36076 Human_SNP_ID_607837325 A-to-I Human chr16 - 71785410 71785410 71785410 CACCACACCCGGCTAATTTTTGTATTTTTGGTAGAGACAGGGTTTCACCATGTTGTCCAGACTAG CACCACACCCGGCTAATTTTTGTATTTTTGGTGGAGACAGGGTTTCACCATGTTGTCCAGACTAG T C AP1G1 Ensembl:ENSG00000166747 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs976445985 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7819,RMVar_hsa_circ_98656,RMVar_hsa_circ_179816,RMVar_hsa_circ_99935,RMVar_hsa_circ_179823,RMVar_hsa_circ_21890,RMVar_hsa_circ_304228,RMVar_hsa_circ_179830,RMVar_hsa_circ_120305,RMVar_hsa_circ_338826,RMVar_hsa_circ_179835,RMVar_hsa_circ_179834,RMVar_hsa_circ_375593,RMVar_hsa_circ_179845,RMVar_hsa_circ_179846,RMVar_hsa_circ_295328 36077 RMVar_ID_36077 Human_SNP_ID_607837350 A-to-I Human chr16 - 71785475 71785475 71785475 CACTACCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGCTACAGGCACCTGC CACTACCCAGGTTCAAGCGATTCTCCTGCCTCCGCCTCCTGAGTAGCTGGGCTACAGGCACCTGC T G AP1G1 Ensembl:ENSG00000166747 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1014452462 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7819,RMVar_hsa_circ_98656,RMVar_hsa_circ_179816,RMVar_hsa_circ_99935,RMVar_hsa_circ_179823,RMVar_hsa_circ_21890,RMVar_hsa_circ_304228,RMVar_hsa_circ_179830,RMVar_hsa_circ_120305,RMVar_hsa_circ_338826,RMVar_hsa_circ_179835,RMVar_hsa_circ_179834,RMVar_hsa_circ_375593,RMVar_hsa_circ_179845,RMVar_hsa_circ_179846,RMVar_hsa_circ_295328 36078 RMVar_ID_36078 Human_SNP_ID_607839187 A-to-I Human chr16 - 71791660 71791656 71791660 TTTTTTTTTTTTTTTTTTTGAGACAGGGTCTCACTCTGTCACCCAGGATACAGTGTCACAGCTTA TTTTTTTTTTTTTTTTTTTGAGACAGGGTCTC____TGTCACCCAGGATACAGTGTCACAGCTTA AGAGT A AP1G1 Ensembl:ENSG00000166747 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1216658233 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_98656,RMVar_hsa_circ_179816,RMVar_hsa_circ_120305,RMVar_hsa_circ_179834,RMVar_hsa_circ_179848,RMVar_hsa_circ_345648 36079 RMVar_ID_36079 Human_SNP_ID_607842668 A-to-I Human chr16 - 71802834 71802834 71802834 TCGCTGGCCAGACCTGGTGGCTCATGTCTGTAATCCCAGTACTTTGGGAAGCCAAGTCAGAAGGA TCGCTGGCCAGACCTGGTGGCTCATGTCTGTATTCCCAGTACTTTGGGAAGCCAAGTCAGAAGGA T A AP1G1 Ensembl:ENSG00000166747 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1319646251 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17564287 RMVar_hsa_circ_98656,RMVar_hsa_circ_179816,RMVar_hsa_circ_120305,RMVar_hsa_circ_179834,RMVar_hsa_circ_345648 36080 RMVar_ID_36080 Human_SNP_ID_607845332 A-to-I Human chr16 + 71810093 71810092 71810094 CACCACGGCCGTCTAATATTTGCATTTTTAGTAGAGAGAGGGTTTCGCCATGTTGGCCAGGCTGG CACCACGGCCGTCTAATATTTGCATTTTTAGT__AGAGAGGGTTTCGCCATGTTGGCCAGGCTGG TAG T L13705-001 RNACentral:URS00005A0C9B misc_RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs997013363 Functional Loss DEL dbSNP153 33..34 33 - - - 36081 RMVar_ID_36081 Human_SNP_ID_607845333 A-to-I Human chr16 + 71810093 71810093 71810093 CACCACGGCCGTCTAATATTTGCATTTTTAGTAGAGAGAGGGTTTCGCCATGTTGGCCAGGCTGG CACCACGGCCGTCTAATATTTGCATTTTTAGTCGAGAGAGGGTTTCGCCATGTTGGCCAGGCTGG A C L13705-001 RNACentral:URS00005A0C9B misc_RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1028946200 Functional Loss SNV dbSNP153 33..33 33 - - - 36082 RMVar_ID_36082 Human_SNP_ID_607846278 A-to-I Human chr16 + 71813290 71813289 71813290 TTTTGTAGAGACACGGTTTTGCCATGTTACCCAAGCTGGTCTGGAACTCATGGGCTCATGCGATC TTTTGTAGAGACACGGTTTTGCCATGTTACCC_AGCTGGTCTGGAACTCATGGGCTCATGCGATC CA C L13705-001 RNACentral:URS00005A0C9B misc_RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1325229196 Functional Loss DEL dbSNP153 33..33 33 - - - 36083 RMVar_ID_36083 Human_SNP_ID_607846632 A-to-I Human chr16 + 71814422 71814422 71814422 TCAAGTGATCCTCCCACCTCAGCCGGGACTACAGGTGCATACCACCATACCCAGCTAATTTTTTT TCAAGTGATCCTCCCACCTCAGCCGGGACTACGGGTGCATACCACCATACCCAGCTAATTTTTTT A G L13705-001 RNACentral:URS00005A0C9B misc_RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1393145547 Functional Loss SNV dbSNP153 33..33 33 - - - 36084 RMVar_ID_36084 Human_SNP_ID_607862469 A-to-I Human chr16 - 71872034 71872034 71872034 CTGAGGTTGGGAGTTCGAGACCAGCCTGACCAACATGGAGAAACCCCGTCTCTACTAAAAATACA CTGAGGTTGGGAGTTCGAGACCAGCCTGACCAGCATGGAGAAACCCCGTCTCTACTAAAAATACA T C ZNF821 Ensembl:ENSG00000102984 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1372191046 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22405,RMVar_hsa_circ_44293 36085 RMVar_ID_36085 Human_SNP_ID_607869941 A-to-I Human chr16 + 71896854 71896854 71896854 ATAAAAACAGCCAGGCGTGGAGGCCCGCATCTATAGTCCAGGAGGCTGAGGTAGGAGGATTGCTT ATAAAAACAGCCAGGCGTGGAGGCCCGCATCTGTAGTCCAGGAGGCTGAGGTAGGAGGATTGCTT A G IST1 Ensembl:ENSG00000182149 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1010588490 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25227197 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 36086 RMVar_ID_36086 Human_SNP_ID_607871507 A-to-I Human chr16 + 71901420 71901420 71901420 TGTTTTTAGTAGAGATGGGGTTTCACTGCGTTAGCCAGAATGGTCTCGATCTCCTGACCTCGTGA TGTTTTTAGTAGAGATGGGGTTTCACTGCGTTCGCCAGAATGGTCTCGATCTCCTGACCTCGTGA A C IST1 Ensembl:ENSG00000182149 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs542740292 Functional Loss SNV dbSNP153 33..33 33 - - - 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 36087 RMVar_ID_36087 Human_SNP_ID_607871508 A-to-I Human chr16 + 71901420 71901420 71901420 TGTTTTTAGTAGAGATGGGGTTTCACTGCGTTAGCCAGAATGGTCTCGATCTCCTGACCTCGTGA TGTTTTTAGTAGAGATGGGGTTTCACTGCGTTTGCCAGAATGGTCTCGATCTCCTGACCTCGTGA A T IST1 Ensembl:ENSG00000182149 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs542740292 Functional Loss SNV dbSNP153 33..33 33 - - - 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 36088 RMVar_ID_36088 Human_SNP_ID_607873277 A-to-I Human chr16 + 71906909 71906909 71906909 TTGTCAGCTGGGTACGGTTGTCTCATGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGGGA TTGTCAGCTGGGTACGGTTGTCTCATGCCTGTCGTCCCAGCTACTTGGGAGGCTGAGGCAGGGGA A C IST1 Ensembl:ENSG00000182149 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs920584904 Functional Loss SNV dbSNP153 33..33 33 - - - 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 36089 RMVar_ID_36089 Human_SNP_ID_607874671 A-to-I Human chr16 + 71911118 71911118 71911118 AAAAAATTAGCTAGGCGTGGTGGTGTGTGCCTATAATCTCAGTTACTTGGGAGGCTGAGGCAGGA AAAAAATTAGCTAGGCGTGGTGGTGTGTGCCTGTAATCTCAGTTACTTGGGAGGCTGAGGCAGGA A G IST1 Ensembl:ENSG00000182149 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs879931609 Functional Loss SNV dbSNP153 33..33 33 - - - 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 36090 RMVar_ID_36090 Human_SNP_ID_607874672 A-to-I Human chr16 + 71911118 71911118 71911118 AAAAAATTAGCTAGGCGTGGTGGTGTGTGCCTATAATCTCAGTTACTTGGGAGGCTGAGGCAGGA AAAAAATTAGCTAGGCGTGGTGGTGTGTGCCTTTAATCTCAGTTACTTGGGAGGCTGAGGCAGGA A T IST1 Ensembl:ENSG00000182149 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs879931609 Functional Loss SNV dbSNP153 33..33 33 - - - 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 36091 RMVar_ID_36091 Human_SNP_ID_607874678 A-to-I Human chr16 + 71911130 71911130 71911130 AGGCGTGGTGGTGTGTGCCTATAATCTCAGTTACTTGGGAGGCTGAGGCAGGAGAATAGCTTAAA AGGCGTGGTGGTGTGTGCCTATAATCTCAGTTGCTTGGGAGGCTGAGGCAGGAGAATAGCTTAAA A G IST1 Ensembl:ENSG00000182149 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1485339983 Functional Loss SNV dbSNP153 33..33 33 - - - 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 36092 RMVar_ID_36092 Human_SNP_ID_607874772 A-to-I Human chr16 + 71911412 71911412 71911412 AAGTTCAGCCAGGTGTGGTGGTTCACGCCTGTAATCCCAGACACTCCGGAGGCTGAGGCAAGAGA AAGTTCAGCCAGGTGTGGTGGTTCACGCCTGTTATCCCAGACACTCCGGAGGCTGAGGCAAGAGA A T IST1 Ensembl:ENSG00000182149 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs12922574 Functional Loss SNV dbSNP153 33..33 33 - - - 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 36093 RMVar_ID_36093 Human_SNP_ID_607875067 A-to-I Human chr16 + 71912263 71912255 71912264 TCTCCATTATAAAAATTTTTTTTTTGAGACGGAATCTCGCTCTGTCACTCAGGCTGGAGTGCGGT TCTCCATTATAAAAATTTTTTTTTT_________TCTCGCTCTGTCACTCAGGCTGGAGTGCGGT TGAGACGGAA T IST1 Ensembl:ENSG00000182149 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1221191306 Functional Loss DEL dbSNP153 26..34 33 - - - Human_RBP_ID_12803795 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 36094 RMVar_ID_36094 Human_SNP_ID_607875071 A-to-I Human chr16 + 71912263 71912263 71912263 TCTCCATTATAAAAATTTTTTTTTTGAGACGGAATCTCGCTCTGTCACTCAGGCTGGAGTGCGGT TCTCCATTATAAAAATTTTTTTTTTGAGACGGTATCTCGCTCTGTCACTCAGGCTGGAGTGCGGT A T IST1 Ensembl:ENSG00000182149 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs532432483 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12803795 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 36095 RMVar_ID_36095 Human_SNP_ID_607879791 A-to-I Human chr16 + 71925590 71925590 71925590 CCTGCCTCAGCCTCCCAAAGTGCTGAGATTACAGGCATGAGCCACCGTGCCCGGCCAGCTCAGTG CCTGCCTCAGCCTCCCAAAGTGCTGAGATTACGGGCATGAGCCACCGTGCCCGGCCAGCTCAGTG A G IST1 Ensembl:ENSG00000182149 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs921309519 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92307,RMVar_hsa_circ_179852,RMVar_hsa_circ_104862,RMVar_hsa_circ_179858,RMVar_hsa_circ_126161,RMVar_hsa_circ_116260,RMVar_hsa_circ_179863,RMVar_hsa_circ_113347,RMVar_hsa_circ_179864,RMVar_hsa_circ_179865 36096 RMVar_ID_36096 Human_SNP_ID_607879826 A-to-I Human chr16 + 71925696 71925696 71925696 TAAAAAAGTACTGGCCAGGTGTGGTGATTCACATTTGTAATCCAAGCACTTTGGGAAGCTGAGGC TAAAAAAGTACTGGCCAGGTGTGGTGATTCACTTTTGTAATCCAAGCACTTTGGGAAGCTGAGGC A T IST1 Ensembl:ENSG00000182149 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1567475494 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92307,RMVar_hsa_circ_179852,RMVar_hsa_circ_104862,RMVar_hsa_circ_179858,RMVar_hsa_circ_126161,RMVar_hsa_circ_116260,RMVar_hsa_circ_179863,RMVar_hsa_circ_113347,RMVar_hsa_circ_179864,RMVar_hsa_circ_179865 36097 RMVar_ID_36097 Human_SNP_ID_607879828 A-to-I Human chr16 + 71925702 71925699 71925702 AGTACTGGCCAGGTGTGGTGATTCACATTTGTAATCCAAGCACTTTGGGAAGCTGAGGCAGGAGG AGTACTGGCCAGGTGTGGTGATTCACATTT___ATCCAAGCACTTTGGGAAGCTGAGGCAGGAGG TGTA T IST1 Ensembl:ENSG00000182149 Protein coding intron GSE47997;GSE126723:GSM3611827,GSM3611828,GSM3611829 K562 cells&HepG2 cells;Bronchiolar epithelium,BEP2D cell line - 23474544,31158229 RNA-Seq:(High) rs10537526 Functional Loss DEL dbSNP153 31..33 33 - - - RMVar_hsa_circ_92307,RMVar_hsa_circ_179852,RMVar_hsa_circ_104862,RMVar_hsa_circ_179858,RMVar_hsa_circ_126161,RMVar_hsa_circ_116260,RMVar_hsa_circ_179863,RMVar_hsa_circ_113347,RMVar_hsa_circ_179864,RMVar_hsa_circ_179865 36098 RMVar_ID_36098 Human_SNP_ID_607908146 A-to-I Human chr16 + 72005140 72005140 72005140 TCCATCAGCCCTGATAGTGCCCAACAGGGCTTAGCGCTGGCTGACAACATGAGACAAGAAAGCAT TCCATCAGCCCTGATAGTGCCCAACAGGGCTTGGCGCTGGCTGACAACATGAGACAAGAAAGCAT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs544278998 Functional Loss SNV dbSNP153 33..33 33 - - - 36099 RMVar_ID_36099 Human_SNP_ID_607908607 A-to-I Human chr16 - 72006640 72006640 72006640 GCGGCCGTAGCCCGTGACCTCACTCGGTGGGCAGGACTGGTCTCCAGAAATGCTTTGGGTTCATC GCGGCCGTAGCCCGTGACCTCACTCGGTGGGCCGGACTGGTCTCCAGAAATGCTTTGGGTTCATC T G - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1463545556 Functional Loss SNV dbSNP153 33..33 33 - - - 36100 RMVar_ID_36100 Human_SNP_ID_607909724 A-to-I Human chr16 + 72010000 72010000 72010000 GAACTATTGGCCTCAAGGGATCTTCCCGCCTCAGCCTCCCAAAGTGGTGGGATTACAGGCGTGGG GAACTATTGGCCTCAAGGGATCTTCCCGCCTCTGCCTCCCAAAGTGGTGGGATTACAGGCGTGGG A T DHODH Ensembl:ENSG00000102967 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1476246092 Functional Loss SNV dbSNP153 33..33 33 - - - 36101 RMVar_ID_36101 Human_SNP_ID_607912392 A-to-I Human chr16 + 72019878 72019878 72019878 AATTGAAAACATTTGGCCGGGCATGGTGGCTCACGCCTGTAATCCTAACACTCTGGAAGGCCAAG AATTGAAAACATTTGGCCGGGCATGGTGGCTCTCGCCTGTAATCCTAACACTCTGGAAGGCCAAG A T DHODH Ensembl:ENSG00000102967 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1365597645 Functional Loss SNV dbSNP153 33..33 33 - - - 36102 RMVar_ID_36102 Human_SNP_ID_607912763 A-to-I Human chr16 - 72020452 72020452 72020452 GCTCGGGAGGCTGAAGTAGGATTGAGGCTCCAATGAACCGTGATCGCGCCACTGCACTCCAGCCT GCTCGGGAGGCTGAAGTAGGATTGAGGCTCCATTGAACCGTGATCGCGCCACTGCACTCCAGCCT T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1321089879 Functional Loss SNV dbSNP153 33..33 33 - - - 36103 RMVar_ID_36103 Human_SNP_ID_607912764 A-to-I Human chr16 - 72020452 72020452 72020452 GCTCGGGAGGCTGAAGTAGGATTGAGGCTCCAATGAACCGTGATCGCGCCACTGCACTCCAGCCT GCTCGGGAGGCTGAAGTAGGATTGAGGCTCCAGTGAACCGTGATCGCGCCACTGCACTCCAGCCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1321089879 Functional Loss SNV dbSNP153 33..33 33 - - - 36104 RMVar_ID_36104 Human_SNP_ID_607912799 A-to-I Human chr16 + 72020541 72020541 72020541 CTGCTCCCGGCTGAGTTTTCAATTATAGAGATAGGGTTTCACCATGTTGCCCAGACTGGTCTTGA CTGCTCCCGGCTGAGTTTTCAATTATAGAGATGGGGTTTCACCATGTTGCCCAGACTGGTCTTGA A G DHODH Ensembl:ENSG00000102967 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs972680163 Functional Loss SNV dbSNP153 33..33 33 - - - 36105 RMVar_ID_36105 Human_SNP_ID_607914166 A-to-I Human chr16 + 72024776 72024776 72024776 GATCACCTGAGGCCAGGAGTTGGAGACCAGCCAGGCCACCATGGTGAAACCCTGTCTCTACCAAA GATCACCTGAGGCCAGGAGTTGGAGACCAGCCGGGCCACCATGGTGAAACCCTGTCTCTACCAAA A G DHODH Ensembl:ENSG00000102967 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs944741177 Functional Loss SNV dbSNP153 33..33 33 - - - 36106 RMVar_ID_36106 Human_SNP_ID_607930628 A-to-I Human chr16 - 72085810 72085810 72085810 TTTATAGAGGCGCAGTTTCACCGTGTTAGCCAAGATGGTCTCGATCTCCTGACCTCGTGATCTGC TTTATAGAGGCGCAGTTTCACCGTGTTAGCCAGGATGGTCTCGATCTCCTGACCTCGTGATCTGC T C TXNL4B Ensembl:ENSG00000140830 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs532012595 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1005450,Human_RBP_ID_6534601,Human_RBP_ID_12804556,Human_RBP_ID_27660266 RMVar_hsa_circ_125389,RMVar_hsa_circ_179871 36107 RMVar_ID_36107 Human_SNP_ID_607981269 A-to-I Human chr16 + 72278289 72278289 72278289 TCGCTGTCACTATGGCCCATTACAAAGCCGCCAACTTGAAGCGTGAGCAGTTCCGGAGGTACTTG TCGCTGTCACTATGGCCCATTACAAAGCCGCCGACTTGAAGCGTGAGCAGTTCCGGAGGTACTTG A G AC009075.2 Ensembl:ENSG00000261774 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1199657194 Functional Loss SNV dbSNP153 33..33 33 - - - 36108 RMVar_ID_36108 Human_SNP_ID_607981280 A-to-I Human chr16 + 72278330 72278329 72278330 CGTGAGCAGTTCCGGAGGTACTTGGAGAAGTCAGGGGTGCTGGACACACTGACCAAGGTGTTGGT CGTGAGCAGTTCCGGAGGTACTTGGAGAAGTC_GGGGTGCTGGACACACTGACCAAGGTGTTGGT CA C AC009075.2 Ensembl:ENSG00000261774 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285500025 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5573414 36109 RMVar_ID_36109 Human_SNP_ID_607981282 A-to-I Human chr16 + 72278330 72278330 72278330 CGTGAGCAGTTCCGGAGGTACTTGGAGAAGTCAGGGGTGCTGGACACACTGACCAAGGTGTTGGT CGTGAGCAGTTCCGGAGGTACTTGGAGAAGTCGGGGGTGCTGGACACACTGACCAAGGTGTTGGT A G AC009075.2 Ensembl:ENSG00000261774 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1405766077 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5573414 36110 RMVar_ID_36110 Human_SNP_ID_607981287 A-to-I Human chr16 + 72278345 72278345 72278345 AGGTACTTGGAGAAGTCAGGGGTGCTGGACACACTGACCAAGGTGTTGGTATGAAGAACCAGAGA AGGTACTTGGAGAAGTCAGGGGTGCTGGACACGCTGACCAAGGTGTTGGTATGAAGAACCAGAGA A G AC009075.2 Ensembl:ENSG00000261774 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1467811907 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5573414 36111 RMVar_ID_36111 Human_SNP_ID_608140119 A-to-I Human chr16 - 72851692 72851692 72851692 ACAAAAATTAGCCGTGGTGGTAGGGGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAA ACAAAAATTAGCCGTGGTGGTAGGGGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAA T C ZFHX3 Ensembl:ENSG00000140836 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1197515989 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26118,RMVar_hsa_circ_356925,RMVar_hsa_circ_369293,RMVar_hsa_circ_81898,RMVar_hsa_circ_179896,RMVar_hsa_circ_179897,RMVar_hsa_circ_179895,RMVar_hsa_circ_69619,RMVar_hsa_circ_179898,RMVar_hsa_circ_374150,RMVar_hsa_circ_300011 36112 RMVar_ID_36112 Human_SNP_ID_608145145 A-to-I Human chr16 - 72870353 72870353 72870353 CTCTGTAGCTCTGTCACCCAGGCTGGAGTGCAATGGCGAGATCTTGGCTCACTGCAACCTCCACC CTCTGTAGCTCTGTCACCCAGGCTGGAGTGCACTGGCGAGATCTTGGCTCACTGCAACCTCCACC T G ZFHX3 Ensembl:ENSG00000140836 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1047485160 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26118,RMVar_hsa_circ_356925,RMVar_hsa_circ_369293,RMVar_hsa_circ_81898,RMVar_hsa_circ_179896,RMVar_hsa_circ_179897,RMVar_hsa_circ_179895,RMVar_hsa_circ_69619,RMVar_hsa_circ_179898,RMVar_hsa_circ_374150,RMVar_hsa_circ_300011 36113 RMVar_ID_36113 Human_SNP_ID_608163891 A-to-I Human chr16 - 72933957 72933957 72933957 AAAATTAGCTGGGCGTGGTGGAGGGCACCTGCAGTCCCAGCTACTCGGGAGGCTGAGGTGGGAGA AAAATTAGCTGGGCGTGGTGGAGGGCACCTGCGGTCCCAGCTACTCGGGAGGCTGAGGTGGGAGA T C ZFHX3 Ensembl:ENSG00000140836 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs537292293 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_65726,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_179900,RMVar_hsa_circ_179901 36114 RMVar_ID_36114 Human_SNP_ID_608184270 A-to-I Human chr16 - 73004277 73004277 73004277 CAGATAGAGAAAAATGGAGGCCAGGCACAGTAATCCTAGCACTTTGGGAGGCTGAGGTGGGAGGA CAGATAGAGAAAAATGGAGGCCAGGCACAGTAGTCCTAGCACTTTGGGAGGCTGAGGTGGGAGGA T C ZFHX3 Ensembl:ENSG00000140836 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1467361155 Functional Loss SNV dbSNP153 33..33 33 - - - 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 36115 RMVar_ID_36115 Human_SNP_ID_608184667 A-to-I Human chr16 - 73005668 73005668 73005668 CTTCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCGGCCACCACGCCCGGCTAATTTGT CTTCTGCCTCAGCCTCCCGAGTAGCTGGGACTGCAGGCGCCGGCCACCACGCCCGGCTAATTTGT T C ZFHX3,AC002044.3 Ensembl:ENSG00000140836,Ensembl:ENSG00000280092 Protein coding,Other intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1453798321 Functional Loss SNV dbSNP153 33..33 33 - - - 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 36116 RMVar_ID_36116 Human_SNP_ID_608185212 A-to-I Human chr16 - 73007651 73007651 73007651 CACGAGGTCAGGAGTTGAGACCTGTCTGGCCAACATAGTGAAACCCAGTCTCTACTAAAGATACA CACGAGGTCAGGAGTTGAGACCTGTCTGGCCAGCATAGTGAAACCCAGTCTCTACTAAAGATACA T C ZFHX3 Ensembl:ENSG00000140836 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1196408016 Functional Loss SNV dbSNP153 33..33 33 - - - 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 36117 RMVar_ID_36117 Human_SNP_ID_608186320 A-to-I Human chr16 - 73011642 73011642 73011642 ATCCATGCACTGCGACCTCTGCCTCTAGGTTCAAGTGATTCTCCTGCCTCAGCCTCCTGAGTAGC ATCCATGCACTGCGACCTCTGCCTCTAGGTTCGAGTGATTCTCCTGCCTCAGCCTCCTGAGTAGC T C ZFHX3 Ensembl:ENSG00000140836 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1020995094 Functional Loss SNV dbSNP153 33..33 33 - - - 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 36118 RMVar_ID_36118 Human_SNP_ID_608186516 A-to-I Human chr16 - 73012348 73012348 73012348 AGAGGCCAGCCAAGGAATAAACTGTCATGTGCAGTATCACTTGTAGTAGAAAATTTGTCTCTGAT AGAGGCCAGCCAAGGAATAAACTGTCATGTGCGGTATCACTTGTAGTAGAAAATTTGTCTCTGAT T C ZFHX3 Ensembl:ENSG00000140836 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs527426497 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22715394 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 36119 RMVar_ID_36119 Human_SNP_ID_608186522 A-to-I Human chr16 - 73012362 73012362 73012362 AAATGCATACTATCAGAGGCCAGCCAAGGAATAAACTGTCATGTGCAGTATCACTTGTAGTAGAA AAATGCATACTATCAGAGGCCAGCCAAGGAATGAACTGTCATGTGCAGTATCACTTGTAGTAGAA T C ZFHX3 Ensembl:ENSG00000140836 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1297900274 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22715394 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 36120 RMVar_ID_36120 Human_SNP_ID_608186526 A-to-I Human chr16 - 73012383 73012383 73012383 AATGGTGATTCCATATGGTTCAAATGCATACTATCAGAGGCCAGCCAAGGAATAAACTGTCATGT AATGGTGATTCCATATGGTTCAAATGCATACTGTCAGAGGCCAGCCAAGGAATAAACTGTCATGT T C ZFHX3 Ensembl:ENSG00000140836 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968221116 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22715394,Human_RBP_ID_25228100 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 36121 RMVar_ID_36121 Human_SNP_ID_608186536 A-to-I Human chr16 - 73012415 73012413 73012415 TTATTATTTAACAGCTCTAATTTAATAAAAAAAATGGTGATTCCATATGGTTCAAATGCATACTA TTATTATTTAACAGCTCTAATTTAATAAAAAA__TGGTGATTCCATATGGTTCAAATGCATACTA ATT A ZFHX3 Ensembl:ENSG00000140836 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs5817824 Functional Loss DEL dbSNP153 33..34 33 - - - 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 36122 RMVar_ID_36122 Human_SNP_ID_608186537 A-to-I Human chr16 - 73012415 73012413 73012415 TTATTATTTAACAGCTCTAATTTAATAAAAAAAATGGTGATTCCATATGGTTCAAATGCATACTA TTATTATTTAACAGCTCTAATTTAATAAAAAA_ATGGTGATTCCATATGGTTCAAATGCATACTA ATT AT ZFHX3 Ensembl:ENSG00000140836 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs5817824 Functional Loss DEL dbSNP153 33..33 33 - - - 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 36123 RMVar_ID_36123 Human_SNP_ID_608186637 A-to-I Human chr16 - 73012819 73012819 73012819 TTTTGGATTAAATTAGAGTTGTTAATAACATCATGGAAGAACGTGTTAGGTTCTGGGCAAGGATC TTTTGGATTAAATTAGAGTTGTTAATAACATCGTGGAAGAACGTGTTAGGTTCTGGGCAAGGATC T C ZFHX3 Ensembl:ENSG00000140836 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1254123445 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17564299 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 36124 RMVar_ID_36124 Human_SNP_ID_608186661 A-to-I Human chr16 - 73012907 73012907 73012907 ATTTTCTGCTACAAGAGATATTGCAAATGACAATTCATTCCTTGGCTGGCCTCTGATACTATGTA ATTTTCTGCTACAAGAGATATTGCAAATGACAGTTCATTCCTTGGCTGGCCTCTGATACTATGTA T C ZFHX3 Ensembl:ENSG00000140836 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1326687225 Functional Loss SNV dbSNP153 33..33 33 - - - 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 36125 RMVar_ID_36125 Human_SNP_ID_608186667 A-to-I Human chr16 - 73012929 73012929 73012929 TTTCTAGAACCAGCATGGATACATTTTCTGCTACAAGAGATATTGCAAATGACAATTCATTCCTT TTTCTAGAACCAGCATGGATACATTTTCTGCTGCAAGAGATATTGCAAATGACAATTCATTCCTT T C ZFHX3 Ensembl:ENSG00000140836 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982186213 Functional Loss SNV dbSNP153 33..33 33 - - - 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 36126 RMVar_ID_36126 Human_SNP_ID_608186671 A-to-I Human chr16 - 73012953 73012953 73012953 GTGTGTGCATAGGATGGAGCTATGTTTCTAGAACCAGCATGGATACATTTTCTGCTACAAGAGAT GTGTGTGCATAGGATGGAGCTATGTTTCTAGAGCCAGCATGGATACATTTTCTGCTACAAGAGAT T C ZFHX3 Ensembl:ENSG00000140836 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1266558357 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17125160 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 36127 RMVar_ID_36127 Human_SNP_ID_608188194 A-to-I Human chr16 - 73018110 73018108 73018110 GTGATGGCGCATGCCTGTAGTCCCAGCTACTCAAGAGGCTAAGGCGGGAGGATTGCTTGAGCCTG GTGATGGCGCATGCCTGTAGTCCCAGCTACTC__GAGGCTAAGGCGGGAGGATTGCTTGAGCCTG CTT C ZFHX3 Ensembl:ENSG00000140836 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs747949607 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_25228115 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 36128 RMVar_ID_36128 Human_SNP_ID_608188194 A-to-I Human chr16 - 73018109 73018108 73018110 TGATGGCGCATGCCTGTAGTCCCAGCTACTCAAGAGGCTAAGGCGGGAGGATTGCTTGAGCCTGG TGATGGCGCATGCCTGTAGTCCCAGCTACTC__GAGGCTAAGGCGGGAGGATTGCTTGAGCCTGG CTT C ZFHX3 Ensembl:ENSG00000140836 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs747949607 Functional Loss DEL dbSNP153 32..33 33 - - - 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 36129 RMVar_ID_36129 Human_SNP_ID_608192386 A-to-I Human chr16 - 73032185 73032185 73032185 CGATCCTCCCACCTCAGTCCCGCAACCCGAGTAGCTCGGACTGTAGGCATGCATCACCACGTCTG CGATCCTCCCACCTCAGTCCCGCAACCCGAGTGGCTCGGACTGTAGGCATGCATCACCACGTCTG T C ZFHX3 Ensembl:ENSG00000140836 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1317024545 Functional Loss SNV dbSNP153 33..33 33 - - - 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 36130 RMVar_ID_36130 Human_SNP_ID_608554638 A-to-I Human chr16 - 74293788 74293788 74293788 GGATGGTCTCGATTTTGTGATCTGCCTGCCTCAGCCTCCCAAAGTGCTAGGATTATAGGCGTGAA GGATGGTCTCGATTTTGTGATCTGCCTGCCTCCGCCTCCCAAAGTGCTAGGATTATAGGCGTGAA T G AC138627.1 Ensembl:ENSG00000261404 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs186308063 Functional Loss SNV dbSNP153 33..33 33 - - - 36131 RMVar_ID_36131 Human_SNP_ID_608556218 A-to-I Human chr16 + 74298776 74298774 74298777 TGTGCCTGGAGTCTCAGCTACTCGGGAGGCTGAAGTGAGAAGATCACTTGAATCTGAGAGGTAGA TGTGCCTGGAGTCTCAGCTACTCGGGAGGCT___GTGAGAAGATCACTTGAATCTGAGAGGTAGA TGAA T PSMD7 Ensembl:ENSG00000103035 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1454401642 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_17564752 RMVar_hsa_circ_179910,RMVar_hsa_circ_89829 36132 RMVar_ID_36132 Human_SNP_ID_608556220 A-to-I Human chr16 + 74298776 74298776 74298776 TGTGCCTGGAGTCTCAGCTACTCGGGAGGCTGAAGTGAGAAGATCACTTGAATCTGAGAGGTAGA TGTGCCTGGAGTCTCAGCTACTCGGGAGGCTGGAGTGAGAAGATCACTTGAATCTGAGAGGTAGA A G PSMD7 Ensembl:ENSG00000103035 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1567524903 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17564752 RMVar_hsa_circ_179910,RMVar_hsa_circ_89829 36133 RMVar_ID_36133 Human_SNP_ID_608556384 A-to-I Human chr16 + 74299428 74299428 74299428 TGAGACAGGGTCTGCCGAGGCTGGGGTGCAGTAGCACAATCTCAGCTCACTGTAGCTAGCCTCAA TGAGACAGGGTCTGCCGAGGCTGGGGTGCAGTGGCACAATCTCAGCTCACTGTAGCTAGCCTCAA A G PSMD7 Ensembl:ENSG00000103035 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1191702220 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12808238 RMVar_hsa_circ_179910,RMVar_hsa_circ_89829 36134 RMVar_ID_36134 Human_SNP_ID_608556402 A-to-I Human chr16 + 74299515 74299515 74299515 AGTCCCTGCACCTCAGTCCCCCAGCCCCAAGTAGCTGAGACTACAGGCACATCCCCACTATGCCC AGTCCCTGCACCTCAGTCCCCCAGCCCCAAGTCGCTGAGACTACAGGCACATCCCCACTATGCCC A C PSMD7 Ensembl:ENSG00000103035 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1382073547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6536272 RMVar_hsa_circ_179910,RMVar_hsa_circ_89829 36135 RMVar_ID_36135 Human_SNP_ID_608556405 A-to-I Human chr16 + 74299525 74299525 74299525 CCTCAGTCCCCCAGCCCCAAGTAGCTGAGACTACAGGCACATCCCCACTATGCCCGGCTAAGTTT CCTCAGTCCCCCAGCCCCAAGTAGCTGAGACTGCAGGCACATCCCCACTATGCCCGGCTAAGTTT A G PSMD7 Ensembl:ENSG00000103035 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1315058150 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6536272 RMVar_hsa_circ_179910,RMVar_hsa_circ_89829 36136 RMVar_ID_36136 Human_SNP_ID_608556407 A-to-I Human chr16 + 74299531 74299531 74299531 TCCCCCAGCCCCAAGTAGCTGAGACTACAGGCACATCCCCACTATGCCCGGCTAAGTTTTGTATT TCCCCCAGCCCCAAGTAGCTGAGACTACAGGCGCATCCCCACTATGCCCGGCTAAGTTTTGTATT A G PSMD7 Ensembl:ENSG00000103035 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs374658449 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6536272 RMVar_hsa_circ_179910,RMVar_hsa_circ_89829 36137 RMVar_ID_36137 Human_SNP_ID_608556463 A-to-I Human chr16 + 74299641 74299641 74299641 GTCTCAAACTCCTGAGCTCAAGTGATCTGCCCACCTCAGCCTCTCGAAGTGCTGGGATTACAGGC GTCTCAAACTCCTGAGCTCAAGTGATCTGCCCCCCTCAGCCTCTCGAAGTGCTGGGATTACAGGC A C PSMD7 Ensembl:ENSG00000103035 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1174946310 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27445482 Human_Splice_Rec_1739558 Human_miRNA_ID_2715717,Human_miRNA_ID_2873859,Human_miRNA_ID_2981822,Human_miRNA_ID_3051699 RMVar_hsa_circ_92508,RMVar_hsa_circ_179910,RMVar_hsa_circ_89829,RMVar_hsa_circ_179911,RMVar_hsa_circ_179912 36138 RMVar_ID_36138 Human_SNP_ID_608556466 A-to-I Human chr16 + 74299646 74299646 74299646 AAACTCCTGAGCTCAAGTGATCTGCCCACCTCAGCCTCTCGAAGTGCTGGGATTACAGGCATGAG AAACTCCTGAGCTCAAGTGATCTGCCCACCTCGGCCTCTCGAAGTGCTGGGATTACAGGCATGAG A G PSMD7 Ensembl:ENSG00000103035 Protein coding intron GSE38233;GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,32596459 RNA-Seq:(High) rs1373251955 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25228257,Human_RBP_ID_27445482 Human_Splice_Rec_1739558,Human_Splice_Rec_1739559 Human_miRNA_ID_604697,Human_miRNA_ID_2715717,Human_miRNA_ID_3051699 RMVar_hsa_circ_92508,RMVar_hsa_circ_179910,RMVar_hsa_circ_89829,RMVar_hsa_circ_179911,RMVar_hsa_circ_179912 36139 RMVar_ID_36139 Human_SNP_ID_608557351 A-to-I Human chr16 + 74302622 74302622 74302622 AACATTAGCCAGGCATGATGGTCCATGCCTGTATTCCAAGCTACTCAGGAGGCTGAGACGGGAAT AACATTAGCCAGGCATGATGGTCCATGCCTGTCTTCCAAGCTACTCAGGAGGCTGAGACGGGAAT A C PSMD7 Ensembl:ENSG00000103035 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913173818 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101025,RMVar_hsa_circ_92508,RMVar_hsa_circ_179910,RMVar_hsa_circ_89829,RMVar_hsa_circ_319635,RMVar_hsa_circ_179912,RMVar_hsa_circ_82589,RMVar_hsa_circ_126476,RMVar_hsa_circ_179914,RMVar_hsa_circ_179913,RMVar_hsa_circ_179917,RMVar_hsa_circ_76646,RMVar_hsa_circ_179916,RMVar_hsa_circ_371554,RMVar_hsa_circ_179918,RMVar_hsa_circ_179919 36140 RMVar_ID_36140 Human_SNP_ID_608558945 A-to-I Human chr16 - 74307877 74307877 74307877 GCCTAGGCTGGAGTGCAGTGGCATGTGATCACAGCTCACTGTAACCTTGAGCTCCTGGGCTCCAG GCCTAGGCTGGAGTGCAGTGGCATGTGATCACGGCTCACTGTAACCTTGAGCTCCTGGGCTCCAG T C AC009120.2 Ensembl:ENSG00000259972 lincRNA intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs542803807 Functional Loss SNV dbSNP153 33..33 33 - - - 36141 RMVar_ID_36141 Human_SNP_ID_608560802 A-to-I Human chr16 - 74313971 74313971 74313971 AAGAAAAAAAAAAAGAAAATGAGGAAGAGGCCAGACACGGGGGCTGACACCTGTAATCTCAGCAC AAGAAAAAAAAAAAGAAAATGAGGAAGAGGCCGGACACGGGGGCTGACACCTGTAATCTCAGCAC T C AC009120.2 Ensembl:ENSG00000259972 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1380810238 Functional Loss SNV dbSNP153 33..33 33 - - - 36142 RMVar_ID_36142 Human_SNP_ID_608561518 A-to-I Human chr16 - 74316084 74316084 74316084 GCTGGTCTCTCTCCTGACCTTGTGATCCACCCACCCTTGCCTCCCAGAGTGCTGGGATTACAGGC GCTGGTCTCTCTCCTGACCTTGTGATCCACCCGCCCTTGCCTCCCAGAGTGCTGGGATTACAGGC T C AC009120.2 Ensembl:ENSG00000259972 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941420135 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5097471,Human_RBP_ID_5247424,Human_RBP_ID_22715400 36143 RMVar_ID_36143 Human_SNP_ID_608561522 A-to-I Human chr16 - 74316088 74316088 74316088 CCAGGCTGGTCTCTCTCCTGACCTTGTGATCCACCCACCCTTGCCTCCCAGAGTGCTGGGATTAC CCAGGCTGGTCTCTCTCCTGACCTTGTGATCCGCCCACCCTTGCCTCCCAGAGTGCTGGGATTAC T C AC009120.2 Ensembl:ENSG00000259972 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749819296 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5097471,Human_RBP_ID_5247424,Human_RBP_ID_22715400 36144 RMVar_ID_36144 Human_SNP_ID_608561603 A-to-I Human chr16 - 74316272 74316272 74316272 CTCAGTCTCACTCTCTCATCAGGCTGGAGTGCAGTGGCCCGATCTCGGCTCACTGCATCCTCTAA CTCAGTCTCACTCTCTCATCAGGCTGGAGTGCCGTGGCCCGATCTCGGCTCACTGCATCCTCTAA T G AC009120.2 Ensembl:ENSG00000259972 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs912813526 Functional Loss SNV dbSNP153 33..33 33 - - - 36145 RMVar_ID_36145 Human_SNP_ID_608562139 A-to-I Human chr16 - 74318023 74318023 74318023 GTCTAAGGTGGGGAGACTAGCCTGGGTAACATAGCAAGACACTTGTCTCTACAAAAAATTAGCCA GTCTAAGGTGGGGAGACTAGCCTGGGTAACATGGCAAGACACTTGTCTCTACAAAAAATTAGCCA T C AC009120.2 Ensembl:ENSG00000259972 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1235490782 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5339 36146 RMVar_ID_36146 Human_SNP_ID_608562895 A-to-I Human chr16 - 74320277 74320277 74320277 CCTCAAGGGATCCTCCCGCCTTGGCCTTCCAAAATGCTAGGATTACAGGTGTGAGCCACTGCGCC CCTCAAGGGATCCTCCCGCCTTGGCCTTCCAACATGCTAGGATTACAGGTGTGAGCCACTGCGCC T G AC009120.2 Ensembl:ENSG00000259972 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs915328362 Functional Loss SNV dbSNP153 33..33 33 - - - 36147 RMVar_ID_36147 Human_SNP_ID_608562988 A-to-I Human chr16 - 74320512 74320512 74320512 CTCACTGCAGCCTCAAACTCCTGGGCTCAAGCAATCCTCCCACCTCAGCCTCCCGAGTAGCTGGG CTCACTGCAGCCTCAAACTCCTGGGCTCAAGCCATCCTCCCACCTCAGCCTCCCGAGTAGCTGGG T G AC009120.2 Ensembl:ENSG00000259972 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1347667097 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25228387 36148 RMVar_ID_36148 Human_SNP_ID_608565271 A-to-I Human chr16 - 74327204 74327204 74327204 CTTTTTATTTTTTGTAGAGATGGGTTCTTGCTATGTTGCCTAGACTGGTCTCGAACTCCTGGCTT CTTTTTATTTTTTGTAGAGATGGGTTCTTGCTGTGTTGCCTAGACTGGTCTCGAACTCCTGGCTT T C AC009120.2 Ensembl:ENSG00000259972 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1460867538 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3509946,Human_RBP_ID_25228441 36149 RMVar_ID_36149 Human_SNP_ID_608565526 A-to-I Human chr16 - 74327852 74327852 74327852 GTGATGGCAAGTGCTTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTTGAAACC GTGATGGCAAGTGCTTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTTGAAACC T C AC009120.2 Ensembl:ENSG00000259972 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1440161657 Functional Loss SNV dbSNP153 33..33 33 - - - 36150 RMVar_ID_36150 Human_SNP_ID_608565746 A-to-I Human chr16 - 74328558 74328558 74328558 GGATCGCTTCAGCCCAGAAGTTCAAGACTGCAATGAGCCATGATTGCGCCACTGCACTCCAGCCT GGATCGCTTCAGCCCAGAAGTTCAAGACTGCAGTGAGCCATGATTGCGCCACTGCACTCCAGCCT T C AC009120.2 Ensembl:ENSG00000259972 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs765813532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3509949,Human_RBP_ID_12808887 36151 RMVar_ID_36151 Human_SNP_ID_608565747 A-to-I Human chr16 - 74328558 74328558 74328558 GGATCGCTTCAGCCCAGAAGTTCAAGACTGCAATGAGCCATGATTGCGCCACTGCACTCCAGCCT GGATCGCTTCAGCCCAGAAGTTCAAGACTGCACTGAGCCATGATTGCGCCACTGCACTCCAGCCT T G AC009120.2 Ensembl:ENSG00000259972 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs765813532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3509949,Human_RBP_ID_12808887 36152 RMVar_ID_36152 Human_SNP_ID_608565832 A-to-I Human chr16 - 74328762 74328762 74328762 AATAAATTAACAGATCAGGCGCAGTAGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGC AATAAATTAACAGATCAGGCGCAGTAGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGC T C AC009120.2 Ensembl:ENSG00000259972 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1434995585 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5096769 36153 RMVar_ID_36153 Human_SNP_ID_608565834 A-to-I Human chr16 - 74328769 74328769 74328769 CTCAAAAAATAAATTAACAGATCAGGCGCAGTAGCTCACACCTGTAATCCCAGCACTTTGGGAGG CTCAAAAAATAAATTAACAGATCAGGCGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGG T C AC009120.2 Ensembl:ENSG00000259972 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348420478 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5096769 36154 RMVar_ID_36154 Human_SNP_ID_608566253 A-to-I Human chr16 - 74330106 74330106 74330106 AAATACAAAATTAGGCGTGATAGCGCATGCCTATAATCCCAGCTTCGAGGGAGGCTGAGGCAGGA AAATACAAAATTAGGCGTGATAGCGCATGCCTGTAATCCCAGCTTCGAGGGAGGCTGAGGCAGGA T C AC009120.2 Ensembl:ENSG00000259972 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1323532097 Functional Loss SNV dbSNP153 33..33 33 - - - 36155 RMVar_ID_36155 Human_SNP_ID_608577617 A-to-I Human chr16 - 74362150 74362150 74362150 AGATTAAGTTTGTTAAAACCCTGCCTTGTCCAAGGGCAGTGGTTCATGCCTGTAATCTCAGCACT AGATTAAGTTTGTTAAAACCCTGCCTTGTCCAGGGGCAGTGGTTCATGCCTGTAATCTCAGCACT T C AC009053.2 Ensembl:ENSG00000214331 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1419826444 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107349,RMVar_hsa_circ_179928 36156 RMVar_ID_36156 Human_SNP_ID_608578060 A-to-I Human chr16 - 74363373 74363373 74363373 ATGGCGAAACCCTATCTCTACTAAAAATACAAAAAGTAGCTGGGCGTGGTGGCGCGTACTTATAG ATGGCGAAACCCTATCTCTACTAAAAATACAAGAAGTAGCTGGGCGTGGTGGCGCGTACTTATAG T C AC009053.2 Ensembl:ENSG00000214331 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1420764338 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107349,RMVar_hsa_circ_179928 36157 RMVar_ID_36157 Human_SNP_ID_608578412 A-to-I Human chr16 - 74364263 74364263 74364263 GATATTTTCAAACCCAGAACTGTCCGCCCCCAAAGCCTGGATTCCCTGCCATGCTGGCATGTTGC GATATTTTCAAACCCAGAACTGTCCGCCCCCATAGCCTGGATTCCCTGCCATGCTGGCATGTTGC T A AC009053.2 Ensembl:ENSG00000214331 Pseudogene intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs868622224 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1089310,Human_RBP_ID_3511426,Human_RBP_ID_17079216,Human_RBP_ID_17189174,Human_RBP_ID_17206575,Human_RBP_ID_17565414,Human_RBP_ID_18926562,Human_RBP_ID_21973822,Human_RBP_ID_22523666 RMVar_hsa_circ_107349,RMVar_hsa_circ_179928 36158 RMVar_ID_36158 Human_SNP_ID_608578413 A-to-I Human chr16 - 74364263 74364263 74364263 GATATTTTCAAACCCAGAACTGTCCGCCCCCAAAGCCTGGATTCCCTGCCATGCTGGCATGTTGC GATATTTTCAAACCCAGAACTGTCCGCCCCCAGAGCCTGGATTCCCTGCCATGCTGGCATGTTGC T C AC009053.2 Ensembl:ENSG00000214331 Pseudogene intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs868622224 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1089310,Human_RBP_ID_3511426,Human_RBP_ID_17079216,Human_RBP_ID_17189174,Human_RBP_ID_17206575,Human_RBP_ID_17565414,Human_RBP_ID_18926562,Human_RBP_ID_21973822,Human_RBP_ID_22523666 RMVar_hsa_circ_107349,RMVar_hsa_circ_179928 36159 RMVar_ID_36159 Human_SNP_ID_608578587 A-to-I Human chr16 - 74364699 74364699 74364699 GGGAGGCCAATGTGGGCAGATCACTTGAGGTCAGGAGCTCGAGACCATCCTGGGCAACGTAGTGA GGGAGGCCAATGTGGGCAGATCACTTGAGGTCGGGAGCTCGAGACCATCCTGGGCAACGTAGTGA T C AC009053.2 Ensembl:ENSG00000214331 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1425262782 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9841677,Human_RBP_ID_12809019,Human_RBP_ID_17206670,Human_RBP_ID_18529948 RMVar_hsa_circ_107349,RMVar_hsa_circ_179928 36160 RMVar_ID_36160 Human_SNP_ID_608578782 A-to-I Human chr16 - 74365103 74365103 74365103 AAATTAGTCGGGCACAGTGGCGTGCGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCGGGAGAA AAATTAGTCGGGCACAGTGGCGTGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCGGGAGAA T C AC009053.2 Ensembl:ENSG00000214331 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444696588 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5247303,Human_RBP_ID_8252528,Human_RBP_ID_17372545 RMVar_hsa_circ_107349,RMVar_hsa_circ_179928 36161 RMVar_ID_36161 Human_SNP_ID_608578799 A-to-I Human chr16 - 74365130 74365130 74365130 AAACTCCATCTCTACTAAAAATACAAAAAATTAGTCGGGCACAGTGGCGTGCGCCTGTAATCCCA AAACTCCATCTCTACTAAAAATACAAAAAATTCGTCGGGCACAGTGGCGTGCGCCTGTAATCCCA T G AC009053.2 Ensembl:ENSG00000214331 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1479249454 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_127777,Human_RBP_ID_5247303,Human_RBP_ID_17372545 RMVar_hsa_circ_107349,RMVar_hsa_circ_179928 36162 RMVar_ID_36162 Human_SNP_ID_608578804 A-to-I Human chr16 - 74365155 74365155 74365155 CGAGACCAGCCTGGCCAACATGGTGAAACTCCATCTCTACTAAAAATACAAAAAATTAGTCGGGC CGAGACCAGCCTGGCCAACATGGTGAAACTCCGTCTCTACTAAAAATACAAAAAATTAGTCGGGC T C AC009053.2 Ensembl:ENSG00000214331 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1397781649 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_127777,Human_RBP_ID_17372545 RMVar_hsa_circ_107349,RMVar_hsa_circ_179928 36163 RMVar_ID_36163 Human_SNP_ID_608579187 A-to-I Human chr16 - 74366318 74366318 74366318 GCACTGCAGCCTCCATCTCCCTGGTTGAAGCAATTTTCCTGTCTCAGCCTCCTGAGTAGCTGGGA GCACTGCAGCCTCCATCTCCCTGGTTGAAGCAGTTTTCCTGTCTCAGCCTCCTGAGTAGCTGGGA T C AC009053.2 Ensembl:ENSG00000214331 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934326839 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107349,RMVar_hsa_circ_179928 36164 RMVar_ID_36164 Human_SNP_ID_608605533 A-to-I Human chr16 - 74440769 74440769 74440769 GCAGCTACTTAGGAGGCTGAGGCAGGAGAATCACTTGACCCAGGAGGTGAAAGTTGCAGTGAGCC GCAGCTACTTAGGAGGCTGAGGCAGGAGAATCGCTTGACCCAGGAGGTGAAAGTTGCAGTGAGCC T C RF00017-1020 RNACentral:URS000099BA6B SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1320482765 Functional Loss SNV dbSNP153 33..33 33 - - - 36165 RMVar_ID_36165 Human_SNP_ID_608620798 A-to-I Human chr16 - 74489236 74489236 74489236 AAACTCTGGACCTCAGGTGATCTTCCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTAAG AAACTCTGGACCTCAGGTGATCTTCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTAAG T C GLG1 Ensembl:ENSG00000090863 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs557470974 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2752,RMVar_hsa_circ_268623,RMVar_hsa_circ_371700,RMVar_hsa_circ_179941,RMVar_hsa_circ_45525,RMVar_hsa_circ_104398,RMVar_hsa_circ_179953,RMVar_hsa_circ_26037,RMVar_hsa_circ_15226,RMVar_hsa_circ_66790,RMVar_hsa_circ_355930,RMVar_hsa_circ_350256,RMVar_hsa_circ_67380,RMVar_hsa_circ_39089,RMVar_hsa_circ_358004,RMVar_hsa_circ_315293,RMVar_hsa_circ_358039,RMVar_hsa_circ_369361,RMVar_hsa_circ_108207,RMVar_hsa_circ_20644,RMVar_hsa_circ_291967,RMVar_hsa_circ_179962,RMVar_hsa_circ_179963,RMVar_hsa_circ_179961,RMVar_hsa_circ_342637,RMVar_hsa_circ_368884,RMVar_hsa_circ_336210 36166 RMVar_ID_36166 Human_SNP_ID_608622354 A-to-I Human chr16 - 74494053 74494053 74494053 CTCCTGCCTCAGCCTCCCTAGTAGCTATGACTACAGGCACCTGACAACACGCCCAGCTAATTTTT CTCCTGCCTCAGCCTCCCTAGTAGCTATGACTGCAGGCACCTGACAACACGCCCAGCTAATTTTT T C GLG1 Ensembl:ENSG00000090863 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1036607075 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2752,RMVar_hsa_circ_268623,RMVar_hsa_circ_371700,RMVar_hsa_circ_179941,RMVar_hsa_circ_104398,RMVar_hsa_circ_179953,RMVar_hsa_circ_26037,RMVar_hsa_circ_15226,RMVar_hsa_circ_66790,RMVar_hsa_circ_355930,RMVar_hsa_circ_350256,RMVar_hsa_circ_67380,RMVar_hsa_circ_358004,RMVar_hsa_circ_369361,RMVar_hsa_circ_108207,RMVar_hsa_circ_179962,RMVar_hsa_circ_179963,RMVar_hsa_circ_342637,RMVar_hsa_circ_336210,RMVar_hsa_circ_179964,RMVar_hsa_circ_345792,RMVar_hsa_circ_349805,RMVar_hsa_circ_347454,RMVar_hsa_circ_359220,RMVar_hsa_circ_55149 36167 RMVar_ID_36167 Human_SNP_ID_608622357 A-to-I Human chr16 - 74494063 74494063 74494063 TCAAGCAAGTCTCCTGCCTCAGCCTCCCTAGTAGCTATGACTACAGGCACCTGACAACACGCCCA TCAAGCAAGTCTCCTGCCTCAGCCTCCCTAGTTGCTATGACTACAGGCACCTGACAACACGCCCA T A GLG1 Ensembl:ENSG00000090863 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs919146592 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2752,RMVar_hsa_circ_268623,RMVar_hsa_circ_371700,RMVar_hsa_circ_179941,RMVar_hsa_circ_104398,RMVar_hsa_circ_179953,RMVar_hsa_circ_26037,RMVar_hsa_circ_15226,RMVar_hsa_circ_66790,RMVar_hsa_circ_355930,RMVar_hsa_circ_350256,RMVar_hsa_circ_67380,RMVar_hsa_circ_358004,RMVar_hsa_circ_369361,RMVar_hsa_circ_108207,RMVar_hsa_circ_179962,RMVar_hsa_circ_179963,RMVar_hsa_circ_342637,RMVar_hsa_circ_336210,RMVar_hsa_circ_179964,RMVar_hsa_circ_345792,RMVar_hsa_circ_349805,RMVar_hsa_circ_347454,RMVar_hsa_circ_359220,RMVar_hsa_circ_55149 36168 RMVar_ID_36168 Human_SNP_ID_608622567 A-to-I Human chr16 - 74494586 74494586 74494586 CCTGGCCAAGATGGTGAAACGCCGTCTCTACTAAAAATACAAAAATTAGTCGGCCGTGGTGGTGG CCTGGCCAAGATGGTGAAACGCCGTCTCTACTGAAAATACAAAAATTAGTCGGCCGTGGTGGTGG T C GLG1 Ensembl:ENSG00000090863 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1567479922 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2752,RMVar_hsa_circ_268623,RMVar_hsa_circ_371700,RMVar_hsa_circ_179941,RMVar_hsa_circ_104398,RMVar_hsa_circ_179953,RMVar_hsa_circ_26037,RMVar_hsa_circ_15226,RMVar_hsa_circ_66790,RMVar_hsa_circ_355930,RMVar_hsa_circ_350256,RMVar_hsa_circ_67380,RMVar_hsa_circ_358004,RMVar_hsa_circ_369361,RMVar_hsa_circ_108207,RMVar_hsa_circ_179962,RMVar_hsa_circ_179963,RMVar_hsa_circ_342637,RMVar_hsa_circ_336210,RMVar_hsa_circ_179964,RMVar_hsa_circ_345792,RMVar_hsa_circ_349805,RMVar_hsa_circ_347454,RMVar_hsa_circ_359220,RMVar_hsa_circ_55149 36169 RMVar_ID_36169 Human_SNP_ID_608646568 A-to-I Human chr16 - 74571500 74571500 74571500 CCTGGCTAATTTTATTATTATTTATAAAGACAAGGTCTCTGAATGTTGCCCAGTCTGGTCTCTAG CCTGGCTAATTTTATTATTATTTATAAAGACAGGGTCTCTGAATGTTGCCCAGTCTGGTCTCTAG T C GLG1 Ensembl:ENSG00000090863 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053069309 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6536664,Human_RBP_ID_12810108 RMVar_hsa_circ_108207,RMVar_hsa_circ_179963 36170 RMVar_ID_36170 Human_SNP_ID_608648754 A-to-I Human chr16 - 74577952 74577952 74577952 TCCAGGCTGGTCTTGAACTCCTGGCCTCAAGTAATCCTCCTACCTTGGCCTCCCAGAGTGCTGGG TCCAGGCTGGTCTTGAACTCCTGGCCTCAAGTGATCCTCCTACCTTGGCCTCCCAGAGTGCTGGG T C GLG1 Ensembl:ENSG00000090863 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs997663948 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25228947 RMVar_hsa_circ_108207,RMVar_hsa_circ_179963 36171 RMVar_ID_36171 Human_SNP_ID_608650247 A-to-I Human chr16 - 74582756 74582756 74582756 GAGTGCAGTGGCGCGATCTCGGCTCACTGTCAAGCTCCACCTCCCGGGTTCACACCATTCTCCTG GAGTGCAGTGGCGCGATCTCGGCTCACTGTCAGGCTCCACCTCCCGGGTTCACACCATTCTCCTG T C GLG1 Ensembl:ENSG00000090863 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1003423903 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6536721 RMVar_hsa_circ_108207,RMVar_hsa_circ_179963 36172 RMVar_ID_36172 Human_SNP_ID_608651298 A-to-I Human chr16 - 74586003 74586003 74586003 GCTAGAGTGCAGTGGTGTGATCTCGGCTCACTACAGCCTTTGCCTCCCGAGTTCAAGCAGTTCTC GCTAGAGTGCAGTGGTGTGATCTCGGCTCACTGCAGCCTTTGCCTCCCGAGTTCAAGCAGTTCTC T C GLG1 Ensembl:ENSG00000090863 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1449594251 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108207,RMVar_hsa_circ_179963 36173 RMVar_ID_36173 Human_SNP_ID_608652135 A-to-I Human chr16 - 74588691 74588691 74588691 GAACAGGCCAAGTGTGGTGGCTCATGTCTGTAATCCGAGCACTTTGGGAGGCTAAGGCGGGTGGA GAACAGGCCAAGTGTGGTGGCTCATGTCTGTATTCCGAGCACTTTGGGAGGCTAAGGCGGGTGGA T A GLG1 Ensembl:ENSG00000090863 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1252655055 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108207,RMVar_hsa_circ_179963 36174 RMVar_ID_36174 Human_SNP_ID_608652661 A-to-I Human chr16 - 74590119 74590119 74590119 GTGGCGTGCGCCTGTAGTCCCTACTACTTGGAAGGCTGAGGCAGGAGAATGGCATGAACCCTGGA GTGGCGTGCGCCTGTAGTCCCTACTACTTGGATGGCTGAGGCAGGAGAATGGCATGAACCCTGGA T A GLG1 Ensembl:ENSG00000090863 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs889431042 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108207,RMVar_hsa_circ_179963 36175 RMVar_ID_36175 Human_SNP_ID_608664304 A-to-I Human chr16 - 74624793 74624793 74624793 TGGATTCTTGCTGTATTGCCCCAGCTGGTCTCAATCTCCTATCCTCAAGCTGTCCTCCCATCTCA TGGATTCTTGCTGTATTGCCCCAGCTGGTCTCCATCTCCTATCCTCAAGCTGTCCTCCCATCTCA T G RFWD3 Ensembl:ENSG00000168411 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs962846436 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82437,RMVar_hsa_circ_125493,RMVar_hsa_circ_103245,RMVar_hsa_circ_117671,RMVar_hsa_circ_179971,RMVar_hsa_circ_179973,RMVar_hsa_circ_81650,RMVar_hsa_circ_179972,RMVar_hsa_circ_179969,RMVar_hsa_circ_179970,RMVar_hsa_circ_179975 36176 RMVar_ID_36176 Human_SNP_ID_608665714 A-to-I Human chr16 - 74629547 74629547 74629547 TCTTGGATCACTGCATCCTCCACCTCCCGAGTAGCTGGGACTATACGCGTGTGCCACCACACCTG TCTTGGATCACTGCATCCTCCACCTCCCGAGTGGCTGGGACTATACGCGTGTGCCACCACACCTG T C RFWD3 Ensembl:ENSG00000168411 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1407171433 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82437,RMVar_hsa_circ_125493,RMVar_hsa_circ_103245,RMVar_hsa_circ_117671,RMVar_hsa_circ_179971,RMVar_hsa_circ_179973,RMVar_hsa_circ_81650,RMVar_hsa_circ_179972,RMVar_hsa_circ_179969,RMVar_hsa_circ_179970,RMVar_hsa_circ_179975,RMVar_hsa_circ_368398,RMVar_hsa_circ_310100,RMVar_hsa_circ_336224,RMVar_hsa_circ_291279,RMVar_hsa_circ_179976,RMVar_hsa_circ_179977,RMVar_hsa_circ_179979,RMVar_hsa_circ_126686,RMVar_hsa_circ_373538,RMVar_hsa_circ_179978 36177 RMVar_ID_36177 Human_SNP_ID_608665725 A-to-I Human chr16 - 74629581 74629580 74629582 ACTCTGTCACCCAGGCTGGAGTGCAGTGGCACAGTCTTGGATCACTGCATCCTCCACCTCCCGAG ACTCTGTCACCCAGGCTGGAGTGCAGTGGCA__GTCTTGGATCACTGCATCCTCCACCTCCCGAG CTG C RFWD3 Ensembl:ENSG00000168411 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1014758301 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_82437,RMVar_hsa_circ_125493,RMVar_hsa_circ_103245,RMVar_hsa_circ_117671,RMVar_hsa_circ_179971,RMVar_hsa_circ_179973,RMVar_hsa_circ_81650,RMVar_hsa_circ_179972,RMVar_hsa_circ_179969,RMVar_hsa_circ_179970,RMVar_hsa_circ_179975,RMVar_hsa_circ_368398,RMVar_hsa_circ_310100,RMVar_hsa_circ_336224,RMVar_hsa_circ_291279,RMVar_hsa_circ_179976,RMVar_hsa_circ_179977,RMVar_hsa_circ_179979,RMVar_hsa_circ_126686,RMVar_hsa_circ_373538,RMVar_hsa_circ_179978 36178 RMVar_ID_36178 Human_SNP_ID_608667134 A-to-I Human chr16 - 74633765 74633765 74633765 TCATATTTTTTGTAGCAACAGGGTTTCACCATATTGCCCAGGCTGGTCTCGAACTCATGATCTCA TCATATTTTTTGTAGCAACAGGGTTTCACCATGTTGCCCAGGCTGGTCTCGAACTCATGATCTCA T C RFWD3 Ensembl:ENSG00000168411 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs894243008 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12811248 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_291279,RMVar_hsa_circ_179976,RMVar_hsa_circ_179977,RMVar_hsa_circ_179979,RMVar_hsa_circ_126686,RMVar_hsa_circ_373538,RMVar_hsa_circ_179978,RMVar_hsa_circ_28231,RMVar_hsa_circ_179981,RMVar_hsa_circ_90685,RMVar_hsa_circ_34417,RMVar_hsa_circ_299985,RMVar_hsa_circ_372830,RMVar_hsa_circ_179980,RMVar_hsa_circ_376320,RMVar_hsa_circ_311118,RMVar_hsa_circ_291016,RMVar_hsa_circ_108742,RMVar_hsa_circ_179984,RMVar_hsa_circ_179986,RMVar_hsa_circ_179987,RMVar_hsa_circ_179985,RMVar_hsa_circ_179983 36179 RMVar_ID_36179 Human_SNP_ID_608669486 A-to-I Human chr16 - 74640624 74640624 74640624 AAAAATTTTTTTTAAAGACAGGGTCTTGCTCTATCACAAAGGCCAGAGTGCAGTGGCGCCATCAG AAAAATTTTTTTTAAAGACAGGGTCTTGCTCTGTCACAAAGGCCAGAGTGCAGTGGCGCCATCAG T C RFWD3 Ensembl:ENSG00000168411 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs567532946 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17881070 RMVar_hsa_circ_109838,RMVar_hsa_circ_82437,RMVar_hsa_circ_125493,RMVar_hsa_circ_103245,RMVar_hsa_circ_179971,RMVar_hsa_circ_179969,RMVar_hsa_circ_179970,RMVar_hsa_circ_336224,RMVar_hsa_circ_28231,RMVar_hsa_circ_372830,RMVar_hsa_circ_179980,RMVar_hsa_circ_376320,RMVar_hsa_circ_311118,RMVar_hsa_circ_108742,RMVar_hsa_circ_179986,RMVar_hsa_circ_179987,RMVar_hsa_circ_179985,RMVar_hsa_circ_371094,RMVar_hsa_circ_369366,RMVar_hsa_circ_71753,RMVar_hsa_circ_179989,RMVar_hsa_circ_179988,RMVar_hsa_circ_347439 36180 RMVar_ID_36180 Human_SNP_ID_608669504 A-to-I Human chr16 - 74640677 74640677 74640677 CCTCGGCCTCCCAGAGTGCTGGGATTACAGGCATGAGCCACTGCGCCTGGCCAAAAAATTTTTTT CCTCGGCCTCCCAGAGTGCTGGGATTACAGGCTTGAGCCACTGCGCCTGGCCAAAAAATTTTTTT T A RFWD3 Ensembl:ENSG00000168411 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs149366908 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109838,RMVar_hsa_circ_82437,RMVar_hsa_circ_125493,RMVar_hsa_circ_103245,RMVar_hsa_circ_179971,RMVar_hsa_circ_179969,RMVar_hsa_circ_179970,RMVar_hsa_circ_336224,RMVar_hsa_circ_28231,RMVar_hsa_circ_372830,RMVar_hsa_circ_179980,RMVar_hsa_circ_376320,RMVar_hsa_circ_311118,RMVar_hsa_circ_108742,RMVar_hsa_circ_179986,RMVar_hsa_circ_179987,RMVar_hsa_circ_179985,RMVar_hsa_circ_371094,RMVar_hsa_circ_369366,RMVar_hsa_circ_71753,RMVar_hsa_circ_179989,RMVar_hsa_circ_179988,RMVar_hsa_circ_347439 36181 RMVar_ID_36181 Human_SNP_ID_608669706 A-to-I Human chr16 - 74641295 74641295 74641295 AGCCGGGCATGGTGGCACGCACCTGTAGTCCCAGCTACTCGGGAGACTGAGGCAGGAGGATAGCT AGCCGGGCATGGTGGCACGCACCTGTAGTCCCCGCTACTCGGGAGACTGAGGCAGGAGGATAGCT T G RFWD3 Ensembl:ENSG00000168411 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs557098025 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109838,RMVar_hsa_circ_82437,RMVar_hsa_circ_125493,RMVar_hsa_circ_103245,RMVar_hsa_circ_179971,RMVar_hsa_circ_179969,RMVar_hsa_circ_179970,RMVar_hsa_circ_336224,RMVar_hsa_circ_28231,RMVar_hsa_circ_372830,RMVar_hsa_circ_179980,RMVar_hsa_circ_376320,RMVar_hsa_circ_311118,RMVar_hsa_circ_108742,RMVar_hsa_circ_179986,RMVar_hsa_circ_179987,RMVar_hsa_circ_179985,RMVar_hsa_circ_371094,RMVar_hsa_circ_369366,RMVar_hsa_circ_71753,RMVar_hsa_circ_179989,RMVar_hsa_circ_179988,RMVar_hsa_circ_347439 36182 RMVar_ID_36182 Human_SNP_ID_608669853 A-to-I Human chr16 - 74641743 74641743 74641743 TTTTTTTGTATTTTTAGTAGAGACAGGGTTTCACCGTGTTGGCCAGGCTGGTCTGGAACTCCTGA TTTTTTTGTATTTTTAGTAGAGACAGGGTTTCTCCGTGTTGGCCAGGCTGGTCTGGAACTCCTGA T A RFWD3 Ensembl:ENSG00000168411 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1017575740 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109838,RMVar_hsa_circ_82437,RMVar_hsa_circ_125493,RMVar_hsa_circ_103245,RMVar_hsa_circ_179971,RMVar_hsa_circ_179969,RMVar_hsa_circ_179970,RMVar_hsa_circ_336224,RMVar_hsa_circ_28231,RMVar_hsa_circ_372830,RMVar_hsa_circ_179980,RMVar_hsa_circ_376320,RMVar_hsa_circ_311118,RMVar_hsa_circ_108742,RMVar_hsa_circ_179986,RMVar_hsa_circ_179987,RMVar_hsa_circ_179985,RMVar_hsa_circ_371094,RMVar_hsa_circ_369366,RMVar_hsa_circ_71753,RMVar_hsa_circ_179989,RMVar_hsa_circ_179988,RMVar_hsa_circ_347439 36183 RMVar_ID_36183 Human_SNP_ID_608669858 A-to-I Human chr16 - 74641757 74641757 74641757 CATGCCCAGCTAATTTTTTTTGTATTTTTAGTAGAGACAGGGTTTCACCGTGTTGGCCAGGCTGG CATGCCCAGCTAATTTTTTTTGTATTTTTAGTGGAGACAGGGTTTCACCGTGTTGGCCAGGCTGG T C RFWD3 Ensembl:ENSG00000168411 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1029616515 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109838,RMVar_hsa_circ_82437,RMVar_hsa_circ_125493,RMVar_hsa_circ_103245,RMVar_hsa_circ_179971,RMVar_hsa_circ_179969,RMVar_hsa_circ_179970,RMVar_hsa_circ_336224,RMVar_hsa_circ_28231,RMVar_hsa_circ_372830,RMVar_hsa_circ_179980,RMVar_hsa_circ_376320,RMVar_hsa_circ_311118,RMVar_hsa_circ_108742,RMVar_hsa_circ_179986,RMVar_hsa_circ_179987,RMVar_hsa_circ_179985,RMVar_hsa_circ_371094,RMVar_hsa_circ_369366,RMVar_hsa_circ_71753,RMVar_hsa_circ_179989,RMVar_hsa_circ_179988,RMVar_hsa_circ_347439 36184 RMVar_ID_36184 Human_SNP_ID_608669872 A-to-I Human chr16 - 74641804 74641804 74641804 CTCCTGCCTCAGTCTCCCAAGTAGCCGGGATTACAGGCGCCTTTCACCATGCCCAGCTAATTTTT CTCCTGCCTCAGTCTCCCAAGTAGCCGGGATTGCAGGCGCCTTTCACCATGCCCAGCTAATTTTT T C RFWD3 Ensembl:ENSG00000168411 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs989418881 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109838,RMVar_hsa_circ_82437,RMVar_hsa_circ_125493,RMVar_hsa_circ_103245,RMVar_hsa_circ_179971,RMVar_hsa_circ_179969,RMVar_hsa_circ_179970,RMVar_hsa_circ_336224,RMVar_hsa_circ_28231,RMVar_hsa_circ_372830,RMVar_hsa_circ_179980,RMVar_hsa_circ_376320,RMVar_hsa_circ_311118,RMVar_hsa_circ_108742,RMVar_hsa_circ_179986,RMVar_hsa_circ_179987,RMVar_hsa_circ_179985,RMVar_hsa_circ_371094,RMVar_hsa_circ_369366,RMVar_hsa_circ_71753,RMVar_hsa_circ_179989,RMVar_hsa_circ_179988,RMVar_hsa_circ_347439 36185 RMVar_ID_36185 Human_SNP_ID_608669886 A-to-I Human chr16 - 74641840 74641840 74641840 TCACTACAACTTCCCGCCTCCCAGGTTCAAGCAATTCTCCTGCCTCAGTCTCCCAAGTAGCCGGG TCACTACAACTTCCCGCCTCCCAGGTTCAAGCCATTCTCCTGCCTCAGTCTCCCAAGTAGCCGGG T G RFWD3 Ensembl:ENSG00000168411 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs201326884 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109838,RMVar_hsa_circ_82437,RMVar_hsa_circ_125493,RMVar_hsa_circ_103245,RMVar_hsa_circ_179971,RMVar_hsa_circ_179969,RMVar_hsa_circ_179970,RMVar_hsa_circ_336224,RMVar_hsa_circ_28231,RMVar_hsa_circ_372830,RMVar_hsa_circ_179980,RMVar_hsa_circ_376320,RMVar_hsa_circ_311118,RMVar_hsa_circ_108742,RMVar_hsa_circ_179986,RMVar_hsa_circ_179987,RMVar_hsa_circ_179985,RMVar_hsa_circ_371094,RMVar_hsa_circ_369366,RMVar_hsa_circ_71753,RMVar_hsa_circ_179989,RMVar_hsa_circ_179988,RMVar_hsa_circ_347439 36186 RMVar_ID_36186 Human_SNP_ID_608669902 A-to-I Human chr16 - 74641888 74641888 74641888 AGTTTTGCTCTTGTTGCCCAGGCTGGATTGCAATGGTGCAATCTTGGCTCACTACAACTTCCCGC AGTTTTGCTCTTGTTGCCCAGGCTGGATTGCAGTGGTGCAATCTTGGCTCACTACAACTTCCCGC T C RFWD3 Ensembl:ENSG00000168411 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs900132705 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109838,RMVar_hsa_circ_82437,RMVar_hsa_circ_125493,RMVar_hsa_circ_103245,RMVar_hsa_circ_179971,RMVar_hsa_circ_179969,RMVar_hsa_circ_179970,RMVar_hsa_circ_336224,RMVar_hsa_circ_28231,RMVar_hsa_circ_372830,RMVar_hsa_circ_179980,RMVar_hsa_circ_376320,RMVar_hsa_circ_311118,RMVar_hsa_circ_108742,RMVar_hsa_circ_179986,RMVar_hsa_circ_179987,RMVar_hsa_circ_179985,RMVar_hsa_circ_371094,RMVar_hsa_circ_369366,RMVar_hsa_circ_71753,RMVar_hsa_circ_179989,RMVar_hsa_circ_179988,RMVar_hsa_circ_347439 36187 RMVar_ID_36187 Human_SNP_ID_608670166 A-to-I Human chr16 - 74642646 74642646 74642646 TCTAATAAAAATGAAAAAAATTATCCGTGTGTAGTGGTACACACCTGTAGTCTCAGCTACTCAGG TCTAATAAAAATGAAAAAAATTATCCGTGTGTTGTGGTACACACCTGTAGTCTCAGCTACTCAGG T A RFWD3 Ensembl:ENSG00000168411 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs542560136 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109838,RMVar_hsa_circ_82437,RMVar_hsa_circ_125493,RMVar_hsa_circ_103245,RMVar_hsa_circ_179971,RMVar_hsa_circ_179969,RMVar_hsa_circ_179970,RMVar_hsa_circ_336224,RMVar_hsa_circ_28231,RMVar_hsa_circ_372830,RMVar_hsa_circ_179980,RMVar_hsa_circ_376320,RMVar_hsa_circ_311118,RMVar_hsa_circ_108742,RMVar_hsa_circ_179986,RMVar_hsa_circ_179987,RMVar_hsa_circ_179985,RMVar_hsa_circ_371094,RMVar_hsa_circ_369366,RMVar_hsa_circ_71753,RMVar_hsa_circ_179989,RMVar_hsa_circ_179988,RMVar_hsa_circ_347439 36188 RMVar_ID_36188 Human_SNP_ID_608670167 A-to-I Human chr16 - 74642646 74642646 74642646 TCTAATAAAAATGAAAAAAATTATCCGTGTGTAGTGGTACACACCTGTAGTCTCAGCTACTCAGG TCTAATAAAAATGAAAAAAATTATCCGTGTGTGGTGGTACACACCTGTAGTCTCAGCTACTCAGG T C RFWD3 Ensembl:ENSG00000168411 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs542560136 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109838,RMVar_hsa_circ_82437,RMVar_hsa_circ_125493,RMVar_hsa_circ_103245,RMVar_hsa_circ_179971,RMVar_hsa_circ_179969,RMVar_hsa_circ_179970,RMVar_hsa_circ_336224,RMVar_hsa_circ_28231,RMVar_hsa_circ_372830,RMVar_hsa_circ_179980,RMVar_hsa_circ_376320,RMVar_hsa_circ_311118,RMVar_hsa_circ_108742,RMVar_hsa_circ_179986,RMVar_hsa_circ_179987,RMVar_hsa_circ_179985,RMVar_hsa_circ_371094,RMVar_hsa_circ_369366,RMVar_hsa_circ_71753,RMVar_hsa_circ_179989,RMVar_hsa_circ_179988,RMVar_hsa_circ_347439 36189 RMVar_ID_36189 Human_SNP_ID_608670212 A-to-I Human chr16 - 74642782 74642782 74642782 TGAGCCTTTTTGAAAATAAATAGGCTGGGTGTAGTGGCTCATGCCTGTAATCCCAGCACTTTGGA TGAGCCTTTTTGAAAATAAATAGGCTGGGTGTGGTGGCTCATGCCTGTAATCCCAGCACTTTGGA T C RFWD3 Ensembl:ENSG00000168411 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs912739783 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109838,RMVar_hsa_circ_82437,RMVar_hsa_circ_125493,RMVar_hsa_circ_103245,RMVar_hsa_circ_179971,RMVar_hsa_circ_179969,RMVar_hsa_circ_179970,RMVar_hsa_circ_336224,RMVar_hsa_circ_28231,RMVar_hsa_circ_372830,RMVar_hsa_circ_179980,RMVar_hsa_circ_376320,RMVar_hsa_circ_311118,RMVar_hsa_circ_108742,RMVar_hsa_circ_179986,RMVar_hsa_circ_179987,RMVar_hsa_circ_179985,RMVar_hsa_circ_371094,RMVar_hsa_circ_369366,RMVar_hsa_circ_71753,RMVar_hsa_circ_179989,RMVar_hsa_circ_179988,RMVar_hsa_circ_347439 36190 RMVar_ID_36190 Human_SNP_ID_608671539 A-to-I Human chr16 - 74646537 74646537 74646537 ATGATCCGCCTGCCTTGGCCTCCCAAAGTGCTAGGATTACAGGTGTGAGCCACTGCGCCCAGCGA ATGATCCGCCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACTGCGCCCAGCGA T C RFWD3 Ensembl:ENSG00000168411 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs891253109 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9836244 RMVar_hsa_circ_109838,RMVar_hsa_circ_82437,RMVar_hsa_circ_125493,RMVar_hsa_circ_103245,RMVar_hsa_circ_179971,RMVar_hsa_circ_179969,RMVar_hsa_circ_179970,RMVar_hsa_circ_28231,RMVar_hsa_circ_179980,RMVar_hsa_circ_311118,RMVar_hsa_circ_108742,RMVar_hsa_circ_179987,RMVar_hsa_circ_371094,RMVar_hsa_circ_71753,RMVar_hsa_circ_179988,RMVar_hsa_circ_347439,RMVar_hsa_circ_179995,RMVar_hsa_circ_296091,RMVar_hsa_circ_320264,RMVar_hsa_circ_272428,RMVar_hsa_circ_179994 36191 RMVar_ID_36191 Human_SNP_ID_608671575 A-to-I Human chr16 - 74646623 74646623 74646623 CGCCGTCATGCCTGGCTAATTTTTTGTATTTTAGTAGAGACGAGGTTTCACCATGTCAGCCAGGA CGCCGTCATGCCTGGCTAATTTTTTGTATTTTGGTAGAGACGAGGTTTCACCATGTCAGCCAGGA T C RFWD3 Ensembl:ENSG00000168411 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1439140380 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109838,RMVar_hsa_circ_82437,RMVar_hsa_circ_125493,RMVar_hsa_circ_103245,RMVar_hsa_circ_179971,RMVar_hsa_circ_179969,RMVar_hsa_circ_179970,RMVar_hsa_circ_28231,RMVar_hsa_circ_179980,RMVar_hsa_circ_311118,RMVar_hsa_circ_108742,RMVar_hsa_circ_179987,RMVar_hsa_circ_371094,RMVar_hsa_circ_71753,RMVar_hsa_circ_179988,RMVar_hsa_circ_347439,RMVar_hsa_circ_179995,RMVar_hsa_circ_296091,RMVar_hsa_circ_320264,RMVar_hsa_circ_272428,RMVar_hsa_circ_179994 36192 RMVar_ID_36192 Human_SNP_ID_608671851 A-to-I Human chr16 - 74647428 74647428 74647428 CAAAAATTAGCCGGATATGGTGGTGCGTGCCTATAGTCCCAGCTACTCGGGAAGCTGAGGCAGGA CAAAAATTAGCCGGATATGGTGGTGCGTGCCTGTAGTCCCAGCTACTCGGGAAGCTGAGGCAGGA T C RFWD3 Ensembl:ENSG00000168411 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1377006123 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109838,RMVar_hsa_circ_82437,RMVar_hsa_circ_125493,RMVar_hsa_circ_103245,RMVar_hsa_circ_179971,RMVar_hsa_circ_179969,RMVar_hsa_circ_179970,RMVar_hsa_circ_28231,RMVar_hsa_circ_179980,RMVar_hsa_circ_311118,RMVar_hsa_circ_108742,RMVar_hsa_circ_179987,RMVar_hsa_circ_371094,RMVar_hsa_circ_71753,RMVar_hsa_circ_179988,RMVar_hsa_circ_347439,RMVar_hsa_circ_179995,RMVar_hsa_circ_296091,RMVar_hsa_circ_320264,RMVar_hsa_circ_272428,RMVar_hsa_circ_179994 36193 RMVar_ID_36193 Human_SNP_ID_608672085 A-to-I Human chr16 - 74648085 74648085 74648085 AGCACATTCGCCAGGTGTGGTGGCATGCGCCTATAGTCCTAGCTACTTAGGGAGTCTGAGACAGG AGCACATTCGCCAGGTGTGGTGGCATGCGCCTGTAGTCCTAGCTACTTAGGGAGTCTGAGACAGG T C RFWD3 Ensembl:ENSG00000168411 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1338719579 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25229332 RMVar_hsa_circ_109838,RMVar_hsa_circ_82437,RMVar_hsa_circ_125493,RMVar_hsa_circ_103245,RMVar_hsa_circ_179971,RMVar_hsa_circ_179969,RMVar_hsa_circ_179970,RMVar_hsa_circ_28231,RMVar_hsa_circ_179980,RMVar_hsa_circ_311118,RMVar_hsa_circ_108742,RMVar_hsa_circ_179987,RMVar_hsa_circ_371094,RMVar_hsa_circ_71753,RMVar_hsa_circ_179988,RMVar_hsa_circ_347439,RMVar_hsa_circ_179995,RMVar_hsa_circ_296091,RMVar_hsa_circ_320264,RMVar_hsa_circ_272428,RMVar_hsa_circ_179994 36194 RMVar_ID_36194 Human_SNP_ID_608672378 A-to-I Human chr16 - 74649051 74649051 74649051 TTTAGAGACTAGGTCTCACTCTCACCCAGGCTAGAGTGCAGTGGTGCAGTCATAACTCACTGCAG TTTAGAGACTAGGTCTCACTCTCACCCAGGCTGGAGTGCAGTGGTGCAGTCATAACTCACTGCAG T C RFWD3 Ensembl:ENSG00000168411 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1329028247 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_888950,Human_RBP_ID_9345911,Human_RBP_ID_12811570,Human_RBP_ID_22652355 RMVar_hsa_circ_109838,RMVar_hsa_circ_82437,RMVar_hsa_circ_125493,RMVar_hsa_circ_103245,RMVar_hsa_circ_179971,RMVar_hsa_circ_179969,RMVar_hsa_circ_179970,RMVar_hsa_circ_28231,RMVar_hsa_circ_179980,RMVar_hsa_circ_311118,RMVar_hsa_circ_108742,RMVar_hsa_circ_179987,RMVar_hsa_circ_371094,RMVar_hsa_circ_71753,RMVar_hsa_circ_179988,RMVar_hsa_circ_347439,RMVar_hsa_circ_179995,RMVar_hsa_circ_296091,RMVar_hsa_circ_320264,RMVar_hsa_circ_272428,RMVar_hsa_circ_179994 36195 RMVar_ID_36195 Human_SNP_ID_608673540 A-to-I Human chr16 - 74652953 74652953 74652953 AATTTGTCTGGGTGTGGTGGCTCATGCCTGCAATTCCAGCATTTTGGGAGGCCAAGGTGGGTGGA AATTTGTCTGGGTGTGGTGGCTCATGCCTGCAGTTCCAGCATTTTGGGAGGCCAAGGTGGGTGGA T C RFWD3 Ensembl:ENSG00000168411 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs918089546 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125493,RMVar_hsa_circ_103245,RMVar_hsa_circ_179969,RMVar_hsa_circ_179970,RMVar_hsa_circ_311118,RMVar_hsa_circ_371094,RMVar_hsa_circ_179988,RMVar_hsa_circ_347439,RMVar_hsa_circ_179995,RMVar_hsa_circ_272428,RMVar_hsa_circ_283239,RMVar_hsa_circ_283448,RMVar_hsa_circ_179998 36196 RMVar_ID_36196 Human_SNP_ID_608673609 A-to-I Human chr16 - 74653151 74653151 74653151 TATTTTTTGTAGAGATGGGGTTTCACCATGTTAATCAGGCTGGTCTCGAACTCCTAGGCACAAGC TATTTTTTGTAGAGATGGGGTTTCACCATGTTCATCAGGCTGGTCTCGAACTCCTAGGCACAAGC T G RFWD3 Ensembl:ENSG00000168411 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs78754429 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6537103,Human_RBP_ID_12811747 RMVar_hsa_circ_125493,RMVar_hsa_circ_103245,RMVar_hsa_circ_179969,RMVar_hsa_circ_179970,RMVar_hsa_circ_311118,RMVar_hsa_circ_371094,RMVar_hsa_circ_179988,RMVar_hsa_circ_347439,RMVar_hsa_circ_179995,RMVar_hsa_circ_272428,RMVar_hsa_circ_283239,RMVar_hsa_circ_283448,RMVar_hsa_circ_179998 36197 RMVar_ID_36197 Human_SNP_ID_608674682 A-to-I Human chr16 - 74656550 74656550 74656550 AGGAGGTTGGGGTGAAAGGTTCCAATGAGCCAATATCATGCCACTGCACTCCAGCCTGGGTGACA AGGAGGTTGGGGTGAAAGGTTCCAATGAGCCAGTATCATGCCACTGCACTCCAGCCTGGGTGACA T C RFWD3 Ensembl:ENSG00000168411 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs966435736 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6537133 RMVar_hsa_circ_125493,RMVar_hsa_circ_103245,RMVar_hsa_circ_179969,RMVar_hsa_circ_179970,RMVar_hsa_circ_311118,RMVar_hsa_circ_371094,RMVar_hsa_circ_179988,RMVar_hsa_circ_347439,RMVar_hsa_circ_179995,RMVar_hsa_circ_272428,RMVar_hsa_circ_283239,RMVar_hsa_circ_283448,RMVar_hsa_circ_179998 36198 RMVar_ID_36198 Human_SNP_ID_608675626 A-to-I Human chr16 - 74659589 74659588 74659590 TTACTCTGGGTTTTTTTTTTGTTTTTAAGACAAGAGTCTTGCTCTGTCACTCAGGCTGGAGTGCA TTACTCTGGGTTTTTTTTTTGTTTTTAAGAC__GAGTCTTGCTCTGTCACTCAGGCTGGAGTGCA CTT C RFWD3 Ensembl:ENSG00000168411 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs765312541 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_125493,RMVar_hsa_circ_103245,RMVar_hsa_circ_179969,RMVar_hsa_circ_179970,RMVar_hsa_circ_311118,RMVar_hsa_circ_371094,RMVar_hsa_circ_179988,RMVar_hsa_circ_347439,RMVar_hsa_circ_179995,RMVar_hsa_circ_272428,RMVar_hsa_circ_283239,RMVar_hsa_circ_283448,RMVar_hsa_circ_179998 36199 RMVar_ID_36199 Human_SNP_ID_608676900 A-to-I Human chr16 - 74663179 74663179 74663179 TGAGTATTGGCCGGGCGCGGTGGCTCATGCCTATAATCCGAGCACTTTGGGAGGCTGAGGCTGGC TGAGTATTGGCCGGGCGCGGTGGCTCATGCCTGTAATCCGAGCACTTTGGGAGGCTGAGGCTGGC T C RFWD3 Ensembl:ENSG00000168411 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs369345096 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12812086 Human_miRNA_ID_1943221,Human_miRNA_ID_1946267,Human_miRNA_ID_2086947,Human_miRNA_ID_2117412,Human_miRNA_ID_2200994,Human_miRNA_ID_2204057,Human_miRNA_ID_2316596,Human_miRNA_ID_2319752,Human_miRNA_ID_2322909,Human_miRNA_ID_2326081,Human_miRNA_ID_2329180,Human_miRNA_ID_2520458,Human_miRNA_ID_2523620,Human_miRNA_ID_2816516,Human_miRNA_ID_2822809,Human_miRNA_ID_2828944,Human_miRNA_ID_2832103,Human_miRNA_ID_2836222,Human_miRNA_ID_2841577,Human_miRNA_ID_2846641,Human_miRNA_ID_2849666,Human_miRNA_ID_2863779,Human_miRNA_ID_3113511 RMVar_hsa_circ_103245,RMVar_hsa_circ_179969,RMVar_hsa_circ_82425,RMVar_hsa_circ_112273,RMVar_hsa_circ_180000,RMVar_hsa_circ_180001 36200 RMVar_ID_36200 Human_SNP_ID_608677228 A-to-I Human chr16 - 74664159 74664159 74664159 GTTGCTTGAGCCGAGGAGTTGAAGACCAGCCTAGGCAACGTGGGAAACCCCATCTATACAAAAAA GTTGCTTGAGCCGAGGAGTTGAAGACCAGCCTGGGCAACGTGGGAAACCCCATCTATACAAAAAA T C RFWD3 Ensembl:ENSG00000168411 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1033078693 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103245,RMVar_hsa_circ_179969,RMVar_hsa_circ_82425,RMVar_hsa_circ_112273,RMVar_hsa_circ_180000,RMVar_hsa_circ_180001 36201 RMVar_ID_36201 Human_SNP_ID_608677257 A-to-I Human chr16 - 74664237 74664237 74664237 ACATTAAAAGCTTTTAGTTAGGCAGCTGCAGTAGCTCACTCCTGTAATCCCAGCACTTTGGGAGG ACATTAAAAGCTTTTAGTTAGGCAGCTGCAGTTGCTCACTCCTGTAATCCCAGCACTTTGGGAGG T A RFWD3 Ensembl:ENSG00000168411 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs939387963 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12812141 RMVar_hsa_circ_103245,RMVar_hsa_circ_179969,RMVar_hsa_circ_82425,RMVar_hsa_circ_112273,RMVar_hsa_circ_180000,RMVar_hsa_circ_180001 36202 RMVar_ID_36202 Human_SNP_ID_608677360 A-to-I Human chr16 - 74664555 74664555 74664555 TTTTGTAGAGACGGGGTTTTGCCGTGTTGCCCAGGCTGGTCTCCAACTCCTGGTCTCCAGCTACC TTTTGTAGAGACGGGGTTTTGCCGTGTTGCCCTGGCTGGTCTCCAACTCCTGGTCTCCAGCTACC T A RFWD3 Ensembl:ENSG00000168411 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1307790256 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103245,RMVar_hsa_circ_179969,RMVar_hsa_circ_82425,RMVar_hsa_circ_112273,RMVar_hsa_circ_180000,RMVar_hsa_circ_180001 36203 RMVar_ID_36203 Human_SNP_ID_608677416 A-to-I Human chr16 - 74664691 74664691 74664691 GGTCTGGAGTGCAGTGGCGTGATCTCGGCTCAATGTAACCTCCACTCTCCGGGTTCAAGGGGTTC GGTCTGGAGTGCAGTGGCGTGATCTCGGCTCAGTGTAACCTCCACTCTCCGGGTTCAAGGGGTTC T C RFWD3 Ensembl:ENSG00000168411 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs546212734 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4384086,Human_RBP_ID_12812156,Human_RBP_ID_19075165,Human_RBP_ID_24558996 Human_Splice_Rec_1740162,Human_Splice_Rec_1740163,Human_Splice_Rec_1740200,Human_Splice_Rec_1740201,Human_Splice_Rec_1740210,Human_Splice_Rec_1740211,Human_Splice_Rec_1740214,Human_Splice_Rec_1740215,Human_Splice_Rec_1740220,Human_Splice_Rec_1740221,Human_Splice_Rec_1740224,Human_Splice_Rec_1740225,Human_Splice_Rec_1740228 RMVar_hsa_circ_103245,RMVar_hsa_circ_179969,RMVar_hsa_circ_82425,RMVar_hsa_circ_112273,RMVar_hsa_circ_180000,RMVar_hsa_circ_180001 36204 RMVar_ID_36204 Human_SNP_ID_608677417 A-to-I Human chr16 - 74664691 74664691 74664691 GGTCTGGAGTGCAGTGGCGTGATCTCGGCTCAATGTAACCTCCACTCTCCGGGTTCAAGGGGTTC GGTCTGGAGTGCAGTGGCGTGATCTCGGCTCACTGTAACCTCCACTCTCCGGGTTCAAGGGGTTC T G RFWD3 Ensembl:ENSG00000168411 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs546212734 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4384086,Human_RBP_ID_12812156,Human_RBP_ID_19075165,Human_RBP_ID_24558996 Human_Splice_Rec_1740162,Human_Splice_Rec_1740163,Human_Splice_Rec_1740200,Human_Splice_Rec_1740201,Human_Splice_Rec_1740210,Human_Splice_Rec_1740211,Human_Splice_Rec_1740214,Human_Splice_Rec_1740215,Human_Splice_Rec_1740220,Human_Splice_Rec_1740221,Human_Splice_Rec_1740224,Human_Splice_Rec_1740225,Human_Splice_Rec_1740228 RMVar_hsa_circ_103245,RMVar_hsa_circ_179969,RMVar_hsa_circ_82425,RMVar_hsa_circ_112273,RMVar_hsa_circ_180000,RMVar_hsa_circ_180001 36205 RMVar_ID_36205 Human_SNP_ID_608677656 A-to-I Human chr16 - 74665330 74665330 74665330 GTCTGCCCTCGGCTTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCGCCTGACCTGTTCTA GTCTGCCCTCGGCTTCCCAAAGTGCTGGGATTGCAGGTGTGAGCCACCGCGCCTGACCTGTTCTA T C RFWD3 Ensembl:ENSG00000168411 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947595304 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20144300 Human_Splice_Rec_1740219 RMVar_hsa_circ_103245,RMVar_hsa_circ_179969,RMVar_hsa_circ_112273,RMVar_hsa_circ_180001 36206 RMVar_ID_36206 Human_SNP_ID_608681935 A-to-I Human chr16 - 74677879 74677879 74677879 GGTCAGGAGTTCAAGACTAGCCTGGCCAACATAGTGAAACACTGTCTCTACTAAAAATACAAAAA GGTCAGGAGTTCAAGACTAGCCTGGCCAACATGGTGAAACACTGTCTCTACTAAAAATACAAAAA T C MLKL Ensembl:ENSG00000168404 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs916287317 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22655,RMVar_hsa_circ_45829 36207 RMVar_ID_36207 Human_SNP_ID_608681937 A-to-I Human chr16 - 74677881 74677881 74677881 GAGGTCAGGAGTTCAAGACTAGCCTGGCCAACATAGTGAAACACTGTCTCTACTAAAAATACAAA GAGGTCAGGAGTTCAAGACTAGCCTGGCCAACGTAGTGAAACACTGTCTCTACTAAAAATACAAA T C MLKL Ensembl:ENSG00000168404 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1332329295 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22655,RMVar_hsa_circ_45829 36208 RMVar_ID_36208 Human_SNP_ID_608687247 A-to-I Human chr16 - 74694530 74694530 74694530 GAACTCCTGGCCTCAAGTGATCCTCTTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCACCTA GAACTCCTGGCCTCAAGTGATCCTCTTGCCTCTGCCTCCCAAAGTGCTGGGATTACAGGCACCTA T A MLKL Ensembl:ENSG00000168404 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs916463006 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74908,RMVar_hsa_circ_94784,RMVar_hsa_circ_180003 36209 RMVar_ID_36209 Human_SNP_ID_608687248 A-to-I Human chr16 - 74694530 74694530 74694530 GAACTCCTGGCCTCAAGTGATCCTCTTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCACCTA GAACTCCTGGCCTCAAGTGATCCTCTTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCACCTA T C MLKL Ensembl:ENSG00000168404 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs916463006 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74908,RMVar_hsa_circ_94784,RMVar_hsa_circ_180003 36210 RMVar_ID_36210 Human_SNP_ID_608739104 A-to-I Human chr16 - 74872503 74872503 74872503 CAGACTGGAGAGTGGTGATGCAATCATAGCTCACTGTAGCCTCTATCACCTGAGCTCAAGTGATC CAGACTGGAGAGTGGTGATGCAATCATAGCTCCCTGTAGCCTCTATCACCTGAGCTCAAGTGATC T G WDR59 Ensembl:ENSG00000103091 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031387093 Functional Loss SNV dbSNP153 33..33 33 - - - 36211 RMVar_ID_36211 Human_SNP_ID_608752048 A-to-I Human chr16 - 74914758 74914758 74914758 AAAACCCCGTCTATACTAAAAATACAAAAATTAGCTGGTCATGGTGGCGTGCGCCTGTAGTCCCG AAAACCCCGTCTATACTAAAAATACAAAAATTGGCTGGTCATGGTGGCGTGCGCCTGTAGTCCCG T C WDR59 Ensembl:ENSG00000103091 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs750953035 Functional Loss SNV dbSNP153 33..33 33 - - - 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_83117,RMVar_hsa_circ_180015,RMVar_hsa_circ_180016,RMVar_hsa_circ_96865,RMVar_hsa_circ_350367,RMVar_hsa_circ_180017,RMVar_hsa_circ_367393,RMVar_hsa_circ_327532,RMVar_hsa_circ_335464,RMVar_hsa_circ_300619,RMVar_hsa_circ_180020,RMVar_hsa_circ_180022,RMVar_hsa_circ_46638,RMVar_hsa_circ_180021,RMVar_hsa_circ_180019 36212 RMVar_ID_36212 Human_SNP_ID_608755473 A-to-I Human chr16 - 74925837 74925837 74925837 AGGTGAGGAGACAGGGTCTTGCTTTGTTGCCCAGGCTGATCTGGAACTCCTGGCCTCAAGTGATC AGGTGAGGAGACAGGGTCTTGCTTTGTTGCCCTGGCTGATCTGGAACTCCTGGCCTCAAGTGATC T A WDR59 Ensembl:ENSG00000103091 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs939155400 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_180033,RMVar_hsa_circ_180035,RMVar_hsa_circ_2684,RMVar_hsa_circ_180036,RMVar_hsa_circ_180034,RMVar_hsa_circ_180032 36213 RMVar_ID_36213 Human_SNP_ID_608755504 A-to-I Human chr16 - 74925941 74925941 74925941 GTGCTCTGTTGCCCACACTGGAGTGCAGTGGTATGATCATAGCTCACTGTAACCTTGAACCCCTT GTGCTCTGTTGCCCACACTGGAGTGCAGTGGTGTGATCATAGCTCACTGTAACCTTGAACCCCTT T C WDR59 Ensembl:ENSG00000103091 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs926187885 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_180033,RMVar_hsa_circ_180035,RMVar_hsa_circ_2684,RMVar_hsa_circ_180036,RMVar_hsa_circ_180034,RMVar_hsa_circ_180032 36214 RMVar_ID_36214 Human_SNP_ID_608759318 A-to-I Human chr16 - 74938691 74938688 74938691 CTAGAAAAAATACAAAAAAATTAGCCAGGCTTAGTGGTGTGCACCTGTAGTCCCAGCTACTTGGA CTAGAAAAAATACAAAAAAATTAGCCAGGCTT___GGTGTGCACCTGTAGTCCCAGCTACTTGGA CACT C WDR59 Ensembl:ENSG00000103091 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1170077849 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_373,RMVar_hsa_circ_8447,RMVar_hsa_circ_180006,RMVar_hsa_circ_90270,RMVar_hsa_circ_348093,RMVar_hsa_circ_115136,RMVar_hsa_circ_180016,RMVar_hsa_circ_96865,RMVar_hsa_circ_350367,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_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_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 36215 RMVar_ID_36215 Human_SNP_ID_608762228 A-to-I Human chr16 - 74947192 74947192 74947192 CACCCGACTTGGCCTCCCAAAGTGCTGGGATTATAGGCTTGAGCCATCGCGACTGGCCCATGGTG CACCCGACTTGGCCTCCCAAAGTGCTGGGATTTTAGGCTTGAGCCATCGCGACTGGCCCATGGTG T A WDR59 Ensembl:ENSG00000103091 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893953074 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_373,RMVar_hsa_circ_8447,RMVar_hsa_circ_180006,RMVar_hsa_circ_90270,RMVar_hsa_circ_348093,RMVar_hsa_circ_115136,RMVar_hsa_circ_180016,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_120143,RMVar_hsa_circ_180033,RMVar_hsa_circ_2684,RMVar_hsa_circ_180034,RMVar_hsa_circ_274537,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,RMVar_hsa_circ_180045,RMVar_hsa_circ_305790,RMVar_hsa_circ_370224,RMVar_hsa_circ_302741,RMVar_hsa_circ_180044 36216 RMVar_ID_36216 Human_SNP_ID_608762229 A-to-I Human chr16 - 74947192 74947192 74947192 CACCCGACTTGGCCTCCCAAAGTGCTGGGATTATAGGCTTGAGCCATCGCGACTGGCCCATGGTG CACCCGACTTGGCCTCCCAAAGTGCTGGGATTGTAGGCTTGAGCCATCGCGACTGGCCCATGGTG T C WDR59 Ensembl:ENSG00000103091 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893953074 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_373,RMVar_hsa_circ_8447,RMVar_hsa_circ_180006,RMVar_hsa_circ_90270,RMVar_hsa_circ_348093,RMVar_hsa_circ_115136,RMVar_hsa_circ_180016,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_120143,RMVar_hsa_circ_180033,RMVar_hsa_circ_2684,RMVar_hsa_circ_180034,RMVar_hsa_circ_274537,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,RMVar_hsa_circ_180045,RMVar_hsa_circ_305790,RMVar_hsa_circ_370224,RMVar_hsa_circ_302741,RMVar_hsa_circ_180044 36217 RMVar_ID_36217 Human_SNP_ID_608766423 A-to-I Human chr16 - 74960542 74960542 74960542 TGGGGTTTTGCTGTGTTGGCCGGGCTGATCTCAAACTCCTGACCTTGGGTGATCCACCCACCTCA TGGGGTTTTGCTGTGTTGGCCGGGCTGATCTCGAACTCCTGACCTTGGGTGATCCACCCACCTCA T C WDR59 Ensembl:ENSG00000103091 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1364314991 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6537443,Human_RBP_ID_12813377 RMVar_hsa_circ_180006,RMVar_hsa_circ_90270,RMVar_hsa_circ_96865,RMVar_hsa_circ_180022,RMVar_hsa_circ_46638,RMVar_hsa_circ_180021,RMVar_hsa_circ_4984,RMVar_hsa_circ_92597,RMVar_hsa_circ_180031,RMVar_hsa_circ_273813,RMVar_hsa_circ_180042,RMVar_hsa_circ_180047,RMVar_hsa_circ_180045,RMVar_hsa_circ_370224,RMVar_hsa_circ_313869,RMVar_hsa_circ_111091,RMVar_hsa_circ_180046,RMVar_hsa_circ_358964,RMVar_hsa_circ_376532 36218 RMVar_ID_36218 Human_SNP_ID_608771743 A-to-I Human chr16 - 74976996 74976994 74976996 CTTTTTCAGTCTTGTTGTTTTTGTTTTCAGACAGGGTCTCGCAATGTCGCCCAGGCTGGAGTGCC CTTTTTCAGTCTTGTTGTTTTTGTTTTCAGAC__GGTCTCGCAATGTCGCCCAGGCTGGAGTGCC CCT C WDR59 Ensembl:ENSG00000103091 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956210940 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_12813616 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 36219 RMVar_ID_36219 Human_SNP_ID_608772851 A-to-I Human chr16 - 74980064 74980064 74980064 ACCTGTGTCAGGAGTCGAGACCAGCCTGGCTAACATGGTGAAAGCCCGTTTCTACTAAAAATACT ACCTGTGTCAGGAGTCGAGACCAGCCTGGCTAGCATGGTGAAAGCCCGTTTCTACTAAAAATACT T C WDR59 Ensembl:ENSG00000103091 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1306022928 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17564318 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 36220 RMVar_ID_36220 Human_SNP_ID_422877629 A-to-I Human chr10 - 15075711 15075711 15075711 CCTTGGCCCCCCAAAGTGCTGAGACTATAGGCATGAGCCACCGCGTCCAGCCAGGATTCTTGAAA CCTTGGCCCCCCAAAGTGCTGAGACTATAGGCGTGAGCCACCGCGTCCAGCCAGGATTCTTGAAA T C ACBD7 Ensembl:ENSG00000176244 Protein coding 3'UTR GSE100210;GSE112787;GSE107867;GSE107867;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;293 Flip-In T-REx cells,empty vector;ASD brains,Fragile X samples from NIH NeuroBioBank;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,29967493,30559470,30559470,32596459 RNA-Seq:(High) rs931755394 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26393942 36221 RMVar_ID_36221 Human_SNP_ID_422877635 A-to-I Human chr10 - 15075730 15075730 15075730 ATCTGAGGTGATCTACCCACCTTGGCCCCCCAAAGTGCTGAGACTATAGGCATGAGCCACCGCGT ATCTGAGGTGATCTACCCACCTTGGCCCCCCAGAGTGCTGAGACTATAGGCATGAGCCACCGCGT T C ACBD7 Ensembl:ENSG00000176244 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs944016661 Functional Loss SNV dbSNP153 33..33 33 - - - 36222 RMVar_ID_36222 Human_SNP_ID_422877648 A-to-I Human chr10 - 15075782 15075782 15075782 TTTCATAGAGACAGGGTTTCACCATGTTGCCCAGGCTGGTCTGGAACTCCTGATCTGAGGTGATC TTTCATAGAGACAGGGTTTCACCATGTTGCCCGGGCTGGTCTGGAACTCCTGATCTGAGGTGATC T C ACBD7 Ensembl:ENSG00000176244 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1298538391 Functional Loss SNV dbSNP153 33..33 33 - - - 36223 RMVar_ID_36223 Human_SNP_ID_422877651 A-to-I Human chr10 - 15075791 15075791 15075791 TTTTGTATTTTTCATAGAGACAGGGTTTCACCATGTTGCCCAGGCTGGTCTGGAACTCCTGATCT TTTTGTATTTTTCATAGAGACAGGGTTTCACCGTGTTGCCCAGGCTGGTCTGGAACTCCTGATCT T C ACBD7 Ensembl:ENSG00000176244 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1441005922 Functional Loss SNV dbSNP153 33..33 33 - - - 36224 RMVar_ID_36224 Human_SNP_ID_422877652 A-to-I Human chr10 - 15075791 15075791 15075791 TTTTGTATTTTTCATAGAGACAGGGTTTCACCATGTTGCCCAGGCTGGTCTGGAACTCCTGATCT TTTTGTATTTTTCATAGAGACAGGGTTTCACCCTGTTGCCCAGGCTGGTCTGGAACTCCTGATCT T G ACBD7 Ensembl:ENSG00000176244 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1441005922 Functional Loss SNV dbSNP153 33..33 33 - - - 36225 RMVar_ID_36225 Human_SNP_ID_422877655 A-to-I Human chr10 - 15075802 15075802 15075802 GCCCAGCTAATTTTTGTATTTTTCATAGAGACAGGGTTTCACCATGTTGCCCAGGCTGGTCTGGA GCCCAGCTAATTTTTGTATTTTTCATAGAGACGGGGTTTCACCATGTTGCCCAGGCTGGTCTGGA T C ACBD7 Ensembl:ENSG00000176244 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1238027320 Functional Loss SNV dbSNP153 33..33 33 - - - 36226 RMVar_ID_36226 Human_SNP_ID_422877683 A-to-I Human chr10 - 15075887 15075887 15075887 TCACTGCAACCTCTGCCTCCCAGGGTCAAGCAATCCTCCCATCTCAGCCTCCAGAGTAGCTGGGA TCACTGCAACCTCTGCCTCCCAGGGTCAAGCAGTCCTCCCATCTCAGCCTCCAGAGTAGCTGGGA T C ACBD7 Ensembl:ENSG00000176244 Protein coding 3'UTR GSE100210;GSE107867;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;ASD brains,frontal_cortex;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,30559470,32596459 RNA-Seq:(High) rs1364687637 Functional Loss SNV dbSNP153 33..33 33 - - - 36227 RMVar_ID_36227 Human_SNP_ID_422877692 A-to-I Human chr10 - 15075911 15075911 15075911 GGAGCGCAGTGGCACGCTCTCGGCTCACTGCAACCTCTGCCTCCCAGGGTCAAGCAATCCTCCCA GGAGCGCAGTGGCACGCTCTCGGCTCACTGCAGCCTCTGCCTCCCAGGGTCAAGCAATCCTCCCA T C ACBD7 Ensembl:ENSG00000176244 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1374547720 Functional Loss SNV dbSNP153 33..33 33 - - - 36228 RMVar_ID_36228 Human_SNP_ID_422877713 A-to-I Human chr10 - 15075968 15075968 15075968 TTCTTTTTTTTTTTTTTTTTTTTTGTTGAGACAGGCTGTCACTCTGTTACCCAGGCTGGAGCGCA TTCTTTTTTTTTTTTTTTTTTTTTGTTGAGACCGGCTGTCACTCTGTTACCCAGGCTGGAGCGCA T G ACBD7 Ensembl:ENSG00000176244 Protein coding 3'UTR GSE100210;GSE107867 HepG2 cell line;ASD brains,cerebellum - 29129909,30559470 RNA-Seq:(High) rs1416678943 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5949838 36229 RMVar_ID_36229 Human_SNP_ID_422878054 A-to-I Human chr10 - 15077225 15077225 15077225 TATGGCTGAGTAATATCCCCTGGTATACATATACAACGTTTTCTTTATCCCATCATCTGCTGATG TATGGCTGAGTAATATCCCCTGGTATACATATGCAACGTTTTCTTTATCCCATCATCTGCTGATG T C ACBD7 Ensembl:ENSG00000176244 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs545234984 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5949854,Human_RBP_ID_17226335,Human_RBP_ID_17343063,Human_RBP_ID_17458844,Human_RBP_ID_17773760,Human_RBP_ID_27605452 36230 RMVar_ID_36230 Human_SNP_ID_422878055 A-to-I Human chr10 - 15077227 15077227 15077227 TATATGGCTGAGTAATATCCCCTGGTATACATATACAACGTTTTCTTTATCCCATCATCTGCTGA TATATGGCTGAGTAATATCCCCTGGTATACATGTACAACGTTTTCTTTATCCCATCATCTGCTGA T C ACBD7 Ensembl:ENSG00000176244 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1393867616 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5949854,Human_RBP_ID_17226335,Human_RBP_ID_17343063,Human_RBP_ID_17458844,Human_RBP_ID_17773760,Human_RBP_ID_27605452 36231 RMVar_ID_36231 Human_SNP_ID_422878217 A-to-I Human chr10 - 15077761 15077761 15077761 TCAAGTGATTCTCTTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGTGCTTGCCACCATGGCTG TCAAGTGATTCTCTTGCCTCAGCCTCCCGAGTGGCTGGGATTACAGGTGCTTGCCACCATGGCTG T C ACBD7 Ensembl:ENSG00000176244 Protein coding 3'UTR GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1160478168 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_374777 36232 RMVar_ID_36232 Human_SNP_ID_422878378 A-to-I Human chr10 - 15078269 15078269 15078269 CATGGAATACTATGGAGCCATAAAAAGGGATGAGTTCATGTCCTTTGCAGGGACATGGATGAAGC CATGGAATACTATGGAGCCATAAAAAGGGATGTGTTCATGTCCTTTGCAGGGACATGGATGAAGC T A ACBD7 Ensembl:ENSG00000176244 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1474632695 Functional Loss SNV dbSNP153 33..33 33 - - - 36233 RMVar_ID_36233 Human_SNP_ID_422886552 A-to-I Human chr10 - 15104471 15104471 15104471 GTGAGGAGGAGGTTGCAGTGAGCTGAGACCGCACCATTGCACTCCAGCCTGGACAACAAGAGTGA GTGAGGAGGAGGTTGCAGTGAGCTGAGACCGCGCCATTGCACTCCAGCCTGGACAACAAGAGTGA T C NMT2 Ensembl:ENSG00000152465 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1180633902 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24856875 36234 RMVar_ID_36234 Human_SNP_ID_422887247 A-to-I Human chr10 - 15106838 15106838 15106838 CCTTGGCCTCCCAAAGTACTGGGATTATAGACATGAGCCACCACTCTTGGCCACAGCCACTTTCA CCTTGGCCTCCCAAAGTACTGGGATTATAGACGTGAGCCACCACTCTTGGCCACAGCCACTTTCA T C NMT2 Ensembl:ENSG00000152465 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 29129909,30559470 RNA-Seq:(High) rs1437975483 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_142336,RMVar_hsa_circ_142337,RMVar_hsa_circ_121941 36235 RMVar_ID_36235 Human_SNP_ID_422887248 A-to-I Human chr10 + 15106843 15106843 15106843 GTGGCTGTGGCCAAGAGTGGTGGCTCATGTCTATAATCCCAGTACTTTGGGAGGCCAAGGCAGAA GTGGCTGTGGCCAAGAGTGGTGGCTCATGTCTGTAATCCCAGTACTTTGGGAGGCCAAGGCAGAA A G RPP38 Ensembl:ENSG00000152464 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941223003 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_142335 36236 RMVar_ID_36236 Human_SNP_ID_422887249 A-to-I Human chr10 - 15106844 15106844 15106844 CTTCTGCCTTGGCCTCCCAAAGTACTGGGATTATAGACATGAGCCACCACTCTTGGCCACAGCCA CTTCTGCCTTGGCCTCCCAAAGTACTGGGATTGTAGACATGAGCCACCACTCTTGGCCACAGCCA T C NMT2 Ensembl:ENSG00000152465 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1323015289 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_142336,RMVar_hsa_circ_142337,RMVar_hsa_circ_121941 36237 RMVar_ID_36237 Human_SNP_ID_422887252 A-to-I Human chr10 - 15106856 15106856 15106856 CCTCAAGTGATCCTTCTGCCTTGGCCTCCCAAAGTACTGGGATTATAGACATGAGCCACCACTCT CCTCAAGTGATCCTTCTGCCTTGGCCTCCCAACGTACTGGGATTATAGACATGAGCCACCACTCT T G NMT2 Ensembl:ENSG00000152465 Protein coding intron GSE107867 ASD brains,cerebellum;ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1055721581 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_142336,RMVar_hsa_circ_142337,RMVar_hsa_circ_121941 36238 RMVar_ID_36238 Human_SNP_ID_422887274 A-to-I Human chr10 - 15106928 15106928 15106928 CCTGGCTAAGTTTTTCATTTTTTGTAGAGACAAGGTCTTGCTATGTTTCCCGTGCTGGTCTTTAA CCTGGCTAAGTTTTTCATTTTTTGTAGAGACAGGGTCTTGCTATGTTTCCCGTGCTGGTCTTTAA T C NMT2 Ensembl:ENSG00000152465 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1323326003 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_142336,RMVar_hsa_circ_142337,RMVar_hsa_circ_121941 36239 RMVar_ID_36239 Human_SNP_ID_422887278 A-to-I Human chr10 - 15106935 15106935 15106935 CACCACGCCTGGCTAAGTTTTTCATTTTTTGTAGAGACAAGGTCTTGCTATGTTTCCCGTGCTGG CACCACGCCTGGCTAAGTTTTTCATTTTTTGTGGAGACAAGGTCTTGCTATGTTTCCCGTGCTGG T C NMT2 Ensembl:ENSG00000152465 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1171931382 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_142336,RMVar_hsa_circ_142337,RMVar_hsa_circ_121941 36240 RMVar_ID_36240 Human_SNP_ID_422887701 A-to-I Human chr10 - 15108386 15108386 15108386 GGTCAGGAGATCGAGACCATTCTGGCCAACATAGTGAAACCCCATCTCTACTAAAAATACAAAAA GGTCAGGAGATCGAGACCATTCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAA T C NMT2 Ensembl:ENSG00000152465 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs527328409 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_142336,RMVar_hsa_circ_142337,RMVar_hsa_circ_121941 36241 RMVar_ID_36241 Human_SNP_ID_422887756 A-to-I Human chr10 - 15108512 15108512 15108512 GGATTGCTTCAAAAGCAGAGTTTTGTGCAAGCACTCACTGTGCTCTCTGAAAGAGCCTGAGGCCG GGATTGCTTCAAAAGCAGAGTTTTGTGCAAGCGCTCACTGTGCTCTCTGAAAGAGCCTGAGGCCG T C NMT2 Ensembl:ENSG00000152465 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs566087410 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_374805 RMVar_hsa_circ_142336,RMVar_hsa_circ_142337,RMVar_hsa_circ_121941 36242 RMVar_ID_36242 Human_SNP_ID_422887757 A-to-I Human chr10 - 15108512 15108512 15108512 GGATTGCTTCAAAAGCAGAGTTTTGTGCAAGCACTCACTGTGCTCTCTGAAAGAGCCTGAGGCCG GGATTGCTTCAAAAGCAGAGTTTTGTGCAAGCCCTCACTGTGCTCTCTGAAAGAGCCTGAGGCCG T G NMT2 Ensembl:ENSG00000152465 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs566087410 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_374805 RMVar_hsa_circ_142336,RMVar_hsa_circ_142337,RMVar_hsa_circ_121941 36243 RMVar_ID_36243 Human_SNP_ID_423000527 A-to-I Human chr10 - 15520149 15520149 15520149 CCTTGGCCTCCCAAAGTGCTAGGATTACAGGCATGAGCCACCGCTCTGGCCTGATCTTTGGATTT CCTTGGCCTCCCAAAGTGCTAGGATTACAGGCGTGAGCCACCGCTCTGGCCTGATCTTTGGATTT T C ITGA8 Ensembl:ENSG00000077943 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs913750507 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38733 36244 RMVar_ID_36244 Human_SNP_ID_423000529 A-to-I Human chr10 - 15520161 15520161 15520161 GCAATCCACCCACCTTGGCCTCCCAAAGTGCTAGGATTACAGGCATGAGCCACCGCTCTGGCCTG GCAATCCACCCACCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCTCTGGCCTG T C ITGA8 Ensembl:ENSG00000077943 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1315233948 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38733 36245 RMVar_ID_36245 Human_SNP_ID_423000537 A-to-I Human chr10 - 15520190 15520190 15520190 CAAGTCTGGTCTCGACCTCCTGAGCTCAGGCAATCCACCCACCTTGGCCTCCCAAAGTGCTAGGA CAAGTCTGGTCTCGACCTCCTGAGCTCAGGCAGTCCACCCACCTTGGCCTCCCAAAGTGCTAGGA T C ITGA8 Ensembl:ENSG00000077943 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1455354399 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38733 36246 RMVar_ID_36246 Human_SNP_ID_423089636 A-to-I Human chr10 - 15847928 15847928 15847928 CTTGCTTTCATTTTTAGGGTTTGTGTTTAGTGAATCAGAGGGATCTGCATTAGAACAGTTTGAAG CTTGCTTTCATTTTTAGGGTTTGTGTTTAGTGGATCAGAGGGATCTGCATTAGAACAGTTTGAAG T C MINDY3 Ensembl:ENSG00000148481 Protein coding exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs781155133 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_374971,Human_RBP_ID_1444840,Human_RBP_ID_1763771,Human_RBP_ID_11321292 Human_Splice_Rec_1115300,Human_Splice_Rec_1115301,Human_Splice_Rec_1115326,Human_Splice_Rec_1115327 RMVar_hsa_circ_142377,RMVar_hsa_circ_94863,RMVar_hsa_circ_368682,RMVar_hsa_circ_142379,RMVar_hsa_circ_23268,RMVar_hsa_circ_333619,RMVar_hsa_circ_281359,RMVar_hsa_circ_142387,RMVar_hsa_circ_286456,RMVar_hsa_circ_272273,RMVar_hsa_circ_142388,RMVar_hsa_circ_142393,RMVar_hsa_circ_272366,RMVar_hsa_circ_4082,RMVar_hsa_circ_142397,RMVar_hsa_circ_285954,RMVar_hsa_circ_142399,RMVar_hsa_circ_142400,RMVar_hsa_circ_312766 36247 RMVar_ID_36247 Human_SNP_ID_423089637 A-to-I Human chr10 - 15847928 15847928 15847928 CTTGCTTTCATTTTTAGGGTTTGTGTTTAGTGAATCAGAGGGATCTGCATTAGAACAGTTTGAAG CTTGCTTTCATTTTTAGGGTTTGTGTTTAGTGCATCAGAGGGATCTGCATTAGAACAGTTTGAAG T G MINDY3 Ensembl:ENSG00000148481 Protein coding exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs781155133 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_374971,Human_RBP_ID_1444840,Human_RBP_ID_1763771,Human_RBP_ID_11321292 Human_Splice_Rec_1115300,Human_Splice_Rec_1115301,Human_Splice_Rec_1115326,Human_Splice_Rec_1115327 RMVar_hsa_circ_142377,RMVar_hsa_circ_94863,RMVar_hsa_circ_368682,RMVar_hsa_circ_142379,RMVar_hsa_circ_23268,RMVar_hsa_circ_333619,RMVar_hsa_circ_281359,RMVar_hsa_circ_142387,RMVar_hsa_circ_286456,RMVar_hsa_circ_272273,RMVar_hsa_circ_142388,RMVar_hsa_circ_142393,RMVar_hsa_circ_272366,RMVar_hsa_circ_4082,RMVar_hsa_circ_142397,RMVar_hsa_circ_285954,RMVar_hsa_circ_142399,RMVar_hsa_circ_142400,RMVar_hsa_circ_312766 36248 RMVar_ID_36248 Human_SNP_ID_423257114 A-to-I Human chr10 + 16437438 16437438 16437438 ACAGCTCACTGCAGCCTCGACCTCCTGAGCTCAAGCGAACTTCCTGCCTCAGCCTCCTGAGCTTC ACAGCTCACTGCAGCCTCGACCTCCTGAGCTCGAGCGAACTTCCTGCCTCAGCCTCCTGAGCTTC A G PTER Ensembl:ENSG00000165983 Protein coding intron GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831 HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line - 29129909,32596459 RNA-Seq:(High) rs11558229 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1115464 36249 RMVar_ID_36249 Human_SNP_ID_423257133 A-to-I Human chr10 + 16437530 16437529 16437531 CCACCATGTCCGGTTATTTTTGTATTTTTTGTAGAGAGTGTCTCGCCATGTTGCCCAGGCTGGTT CCACCATGTCCGGTTATTTTTGTATTTTTTGT__AGAGTGTCTCGCCATGTTGCCCAGGCTGGTT TAG T PTER Ensembl:ENSG00000165983 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs770599177 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_11321779,Human_RBP_ID_22152383 36250 RMVar_ID_36250 Human_SNP_ID_423257500 A-to-I Human chr10 + 16438666 16438666 16438666 TGAGTGGTCTCAGGCCAGGCGCGGTGGCTCACACCTGTAATCCCGGCACTTTGGGAGGCTGAGGC TGAGTGGTCTCAGGCCAGGCGCGGTGGCTCACCCCTGTAATCCCGGCACTTTGGGAGGCTGAGGC A C PTER Ensembl:ENSG00000165983 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1203385466 Functional Loss SNV dbSNP153 33..33 33 - - - 36251 RMVar_ID_36251 Human_SNP_ID_423259450 A-to-I Human chr10 + 16446274 16446274 16446274 GAGTTGGTCTGTCGCCCAGGCTGGAGTGTAGCAGTGTGATCTTGGCTAACTGCAACCTCCACCAC GAGTTGGTCTGTCGCCCAGGCTGGAGTGTAGCGGTGTGATCTTGGCTAACTGCAACCTCCACCAC A G PTER Ensembl:ENSG00000165983 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913795505 Functional Loss SNV dbSNP153 33..33 33 - - - 36252 RMVar_ID_36252 Human_SNP_ID_423261811 A-to-I Human chr10 + 16455296 16455296 16455296 GTTCTCCTGAAGCATCAGACCAAGGGCCAGAAAAAAGAGAAACTTCTGAGCAGAAAAGTACTGCC GTTCTCCTGAAGCATCAGACCAAGGGCCAGAAGAAAGAGAAACTTCTGAGCAGAAAAGTACTGCC A G PTER Ensembl:ENSG00000165983 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1372475680 Functional Loss SNV dbSNP153 33..33 33 - - - 36253 RMVar_ID_36253 Human_SNP_ID_423277351 A-to-I Human chr10 + 16511377 16511377 16511377 ACCTAGGACTAATGACAGATCATTTCCTTCTGATGAGAACTAGGAGGGTTTGCCTTCTCTGAGAC ACCTAGGACTAATGACAGATCATTTCCTTCTGCTGAGAACTAGGAGGGTTTGCCTTCTCTGAGAC A C PTER Ensembl:ENSG00000165983 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs80072752 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18239911 36254 RMVar_ID_36254 Human_SNP_ID_423311861 A-to-I Human chr10 - 16637523 16637523 16637523 CCCCGCCTAAGGATTCTCCAGTATCACACATCATGGCCTGAAAAGACTTCGCAGAACTGAAACTC CCCCGCCTAAGGATTCTCCAGTATCACACATCGTGGCCTGAAAAGACTTCGCAGAACTGAAACTC T C RSU1 Ensembl:ENSG00000148484 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1250340314 Functional Loss SNV dbSNP153 33..33 33 - - - 36255 RMVar_ID_36255 Human_SNP_ID_423336937 A-to-I Human chr10 - 16720904 16720904 16720904 CAGCTCACTGCAGCCTCAAACTCTCAGGGCTCAGGTGATCCTCCCACCTCAGCCTCCCAAGCAGT CAGCTCACTGCAGCCTCAAACTCTCAGGGCTCCGGTGATCCTCCCACCTCAGCCTCCCAAGCAGT T G RSU1 Ensembl:ENSG00000148484 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1344441457 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28778,RMVar_hsa_circ_315868,RMVar_hsa_circ_142402,RMVar_hsa_circ_23051,RMVar_hsa_circ_27954,RMVar_hsa_circ_21833 36256 RMVar_ID_36256 Human_SNP_ID_423340175 A-to-I Human chr10 - 16730962 16730962 16730962 AAAATAAGCTGGGCGTGGTGGCGGGCATCTATAATCCCAGCTACTTCAGAGACTGAGGCACAAGA AAAATAAGCTGGGCGTGGTGGCGGGCATCTATGATCCCAGCTACTTCAGAGACTGAGGCACAAGA T C AC073367.1,RSU1 Ensembl:ENSG00000225213,Ensembl:ENSG00000148484 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs778428404 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28778,RMVar_hsa_circ_315868,RMVar_hsa_circ_142402,RMVar_hsa_circ_23051,RMVar_hsa_circ_27954 36257 RMVar_ID_36257 Human_SNP_ID_423340176 A-to-I Human chr10 - 16730964 16730964 16730964 CAAAAATAAGCTGGGCGTGGTGGCGGGCATCTATAATCCCAGCTACTTCAGAGACTGAGGCACAA CAAAAATAAGCTGGGCGTGGTGGCGGGCATCTGTAATCCCAGCTACTTCAGAGACTGAGGCACAA T C AC073367.1,RSU1 Ensembl:ENSG00000225213,Ensembl:ENSG00000148484 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs977114357 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28778,RMVar_hsa_circ_315868,RMVar_hsa_circ_142402,RMVar_hsa_circ_23051,RMVar_hsa_circ_27954 36258 RMVar_ID_36258 Human_SNP_ID_423342780 A-to-I Human chr10 - 16739595 16739595 16739595 GAAAGAAAGAAAATGTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATGGCGTGAACCTG GAAAGAAAGAAAATGTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCGTGAACCTG T C AC073367.1,RSU1 Ensembl:ENSG00000225213,Ensembl:ENSG00000148484 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs966860953 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28778,RMVar_hsa_circ_315868,RMVar_hsa_circ_23051,RMVar_hsa_circ_27954 36259 RMVar_ID_36259 Human_SNP_ID_423470307 A-to-I Human chr10 - 17217107 17217107 17217107 CTGAGACAGGAGCTTGCAATACCACCCAGGCTAGAATACAGTGACTCCATCACAGCTCACTGTAG CTGAGACAGGAGCTTGCAATACCACCCAGGCTGGAATACAGTGACTCCATCACAGCTCACTGTAG T C VIM-AS1 Ensembl:ENSG00000229124 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs932065095 Functional Loss SNV dbSNP153 33..33 33 - - - 36260 RMVar_ID_36260 Human_SNP_ID_423472926 A-to-I Human chr10 - 17226592 17226592 17226592 GCACACCTGTGGTCCCAGCTACTTGGGAGACTAAGGCAGGGGGATTGCTTGAGCCTGGGAAATTG GCACACCTGTGGTCCCAGCTACTTGGGAGACTGAGGCAGGGGGATTGCTTGAGCCTGGGAAATTG T C VIM-AS1 Ensembl:ENSG00000229124 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1021281174 Functional Loss SNV dbSNP153 33..33 33 - - - 36261 RMVar_ID_36261 Human_SNP_ID_423475406 A-to-I Human chr10 + 17234781 17234781 17234781 GCAGGAGTCCACTGAGTACCGGAGACAGGTGCAGTCCCTCACCTGTGAAGTGGATGCCCTTAAAG GCAGGAGTCCACTGAGTACCGGAGACAGGTGCGGTCCCTCACCTGTGAAGTGGATGCCCTTAAAG A G VIM Ensembl:ENSG00000026025 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs779403092 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_8331149,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_24797606,Human_RBP_ID_26394017,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_2777478,Human_miRNA_ID_2890313,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 36262 RMVar_ID_36262 Human_SNP_ID_423476215 A-to-I Human chr10 + 17237460 17237460 17237460 TCCTACAAGATTTAGAAAAAAGTTTACAACATAATCTAGTTTACAGAAAAATCTTGTGCTAGAAT TCCTACAAGATTTAGAAAAAAGTTTACAACATGATCTAGTTTACAGAAAAATCTTGTGCTAGAAT A G VIM Ensembl:ENSG00000026025 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1014530164 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26062,Human_RBP_ID_375118,Human_RBP_ID_2207326,Human_RBP_ID_3345391,Human_RBP_ID_5951617,Human_RBP_ID_9583727,Human_RBP_ID_17226408,Human_RBP_ID_17343116,Human_RBP_ID_17458935,Human_RBP_ID_17774143,Human_RBP_ID_18239964,Human_RBP_ID_22152431,Human_RBP_ID_22377311,Human_RBP_ID_22879858,Human_RBP_ID_23206371,Human_RBP_ID_23447747,Human_RBP_ID_24401234,Human_RBP_ID_24456689,Human_RBP_ID_26399653,Human_RBP_ID_26877831,Human_RBP_ID_27192277 Human_miRNA_ID_2290411 RMVar_hsa_circ_122742,RMVar_hsa_circ_109688,RMVar_hsa_circ_142425,RMVar_hsa_circ_142426,RMVar_hsa_circ_95446,RMVar_hsa_circ_142435,RMVar_hsa_circ_117850,RMVar_hsa_circ_78427,RMVar_hsa_circ_142437,RMVar_hsa_circ_103579,RMVar_hsa_circ_142438,RMVar_hsa_circ_77198,RMVar_hsa_circ_75842,RMVar_hsa_circ_142443,RMVar_hsa_circ_125809,RMVar_hsa_circ_142446,RMVar_hsa_circ_142447,RMVar_hsa_circ_142449 36263 RMVar_ID_36263 Human_SNP_ID_423476216 A-to-I Human chr10 + 17237460 17237460 17237460 TCCTACAAGATTTAGAAAAAAGTTTACAACATAATCTAGTTTACAGAAAAATCTTGTGCTAGAAT TCCTACAAGATTTAGAAAAAAGTTTACAACATTATCTAGTTTACAGAAAAATCTTGTGCTAGAAT A T VIM Ensembl:ENSG00000026025 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1014530164 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26062,Human_RBP_ID_375118,Human_RBP_ID_2207326,Human_RBP_ID_3345391,Human_RBP_ID_5951617,Human_RBP_ID_9583727,Human_RBP_ID_17226408,Human_RBP_ID_17343116,Human_RBP_ID_17458935,Human_RBP_ID_17774143,Human_RBP_ID_18239964,Human_RBP_ID_22152431,Human_RBP_ID_22377311,Human_RBP_ID_22879858,Human_RBP_ID_23206371,Human_RBP_ID_23447747,Human_RBP_ID_24401234,Human_RBP_ID_24456689,Human_RBP_ID_26399653,Human_RBP_ID_26877831,Human_RBP_ID_27192277 Human_miRNA_ID_2290411 RMVar_hsa_circ_122742,RMVar_hsa_circ_109688,RMVar_hsa_circ_142425,RMVar_hsa_circ_142426,RMVar_hsa_circ_95446,RMVar_hsa_circ_142435,RMVar_hsa_circ_117850,RMVar_hsa_circ_78427,RMVar_hsa_circ_142437,RMVar_hsa_circ_103579,RMVar_hsa_circ_142438,RMVar_hsa_circ_77198,RMVar_hsa_circ_75842,RMVar_hsa_circ_142443,RMVar_hsa_circ_125809,RMVar_hsa_circ_142446,RMVar_hsa_circ_142447,RMVar_hsa_circ_142449 36264 RMVar_ID_36264 Human_SNP_ID_423570477 A-to-I Human chr10 - 17577587 17577587 17577587 AATGCCTGTTAGCCTCACGTAAAATGCCCCCAACATGCGGACATACTTGAAATCTTCATTTTTGA AATGCCTGTTAGCCTCACGTAAAATGCCCCCAGCATGCGGACATACTTGAAATCTTCATTTTTGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1297698710 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_142460,RMVar_hsa_circ_142461 36265 RMVar_ID_36265 Human_SNP_ID_423570588 A-to-I Human chr10 - 17577987 17577987 17577987 TTGGGAGATCGATTCCACCTTCTGGGAGACCGACTCCTACTCCTTCTGTAGCGCAGTGTGGGAGA TTGGGAGATCGATTCCACCTTCTGGGAGACCGGCTCCTACTCCTTCTGTAGCGCAGTGTGGGAGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1403472844 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_142460,RMVar_hsa_circ_142461 36266 RMVar_ID_36266 Human_SNP_ID_423570624 A-to-I Human chr10 + 17578153 17578152 17578154 CCCCAGGTCATCACTGTAGTCACAGACACAAGAACCACTCAAAGTCTCCCGAAAGGTCTTAGAAG CCCCAGGTCATCACTGTAGTCACAGACACAAG__CCACTCAAAGTCTCCCGAAAGGTCTTAGAAG GAA G PRPF38AP2 Ensembl:ENSG00000236582 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1483646334 Functional Loss DEL dbSNP153 33..34 33 - - - 36267 RMVar_ID_36267 Human_SNP_ID_423574856 A-to-I Human chr10 - 17593387 17593387 17593387 CGTTTGAACCTGAGAGGCAGAAGTTGCAGTGAACTGACATGATGCCATTGCATTCCAGCCTGGGC CGTTTGAACCTGAGAGGCAGAAGTTGCAGTGAGCTGACATGATGCCATTGCATTCCAGCCTGGGC T C HACD1 Ensembl:ENSG00000165996 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1306577547 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_142460,RMVar_hsa_circ_142461,RMVar_hsa_circ_142463,RMVar_hsa_circ_142464,RMVar_hsa_circ_377162 36268 RMVar_ID_36268 Human_SNP_ID_423575318 A-to-I Human chr10 - 17595027 17595027 17595027 TGGTGAAACCCTGTCTCTACTAAAAATACAAAAATTAACCGGGCGTGGTGGCGGGCGCCTGTAGT TGGTGAAACCCTGTCTCTACTAAAAATACAAACATTAACCGGGCGTGGTGGCGGGCGCCTGTAGT T G HACD1 Ensembl:ENSG00000165996 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1476548544 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_142460,RMVar_hsa_circ_142461,RMVar_hsa_circ_142463,RMVar_hsa_circ_142465,RMVar_hsa_circ_142464,RMVar_hsa_circ_377162,RMVar_hsa_circ_296986 36269 RMVar_ID_36269 Human_SNP_ID_423575812 A-to-I Human chr10 - 17597200 17597200 17597200 GAGGTTGCAGTGATCTGAGATCACACCACTGCACTCCAGCTTGGTGACACAGCGTGACTCTGTCT GAGGTTGCAGTGATCTGAGATCACACCACTGCCCTCCAGCTTGGTGACACAGCGTGACTCTGTCT T G HACD1 Ensembl:ENSG00000165996 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs782707866 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_142460,RMVar_hsa_circ_142461,RMVar_hsa_circ_142463,RMVar_hsa_circ_142465,RMVar_hsa_circ_142464,RMVar_hsa_circ_377162,RMVar_hsa_circ_296986 36270 RMVar_ID_36270 Human_SNP_ID_423577774 A-to-I Human chr10 - 17604453 17604453 17604453 TTTTTGAGACGGACAGCTCTGTCGCCCAGGCTAGAGTGCAGTGGCGTGATCTTGCCTCACTGCAA TTTTTGAGACGGACAGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCGTGATCTTGCCTCACTGCAA T C HACD1 Ensembl:ENSG00000165996 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1554816878 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115426,RMVar_hsa_circ_142467 36271 RMVar_ID_36271 Human_SNP_ID_423579384 A-to-I Human chr10 - 17610392 17610392 17610392 CACCCACCTTGGCCTCCCAAAATCCTGGGATTACAGGTGTGAGCCACTGCGCCTGGCCTAAAATT CACCCACCTTGGCCTCCCAAAATCCTGGGATTGCAGGTGTGAGCCACTGCGCCTGGCCTAAAATT T C HACD1 Ensembl:ENSG00000165996 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388579416 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115426,RMVar_hsa_circ_142467 36272 RMVar_ID_36272 Human_SNP_ID_423579397 A-to-I Human chr10 - 17610466 17610466 17610466 TTTTAAATTTTTTGTAGAAACAAGGTCTTGCCATGTTGCCCAGGCTGGTCTTGAACTCCTGGGCC TTTTAAATTTTTTGTAGAAACAAGGTCTTGCCGTGTTGCCCAGGCTGGTCTTGAACTCCTGGGCC T C HACD1 Ensembl:ENSG00000165996 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs574174407 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115426,RMVar_hsa_circ_142467 36273 RMVar_ID_36273 Human_SNP_ID_423580532 A-to-I Human chr10 - 17614244 17614244 17614244 TAATAATTTCTGTAAAGACAGGTTTTTGCTATATTGCCCAGGATGTTCTCAAGTGATCCTCCCAC TAATAATTTCTGTAAAGACAGGTTTTTGCTATGTTGCCCAGGATGTTCTCAAGTGATCCTCCCAC T C HACD1 Ensembl:ENSG00000165996 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1389845577 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11323997 RMVar_hsa_circ_115426,RMVar_hsa_circ_142467 36274 RMVar_ID_36274 Human_SNP_ID_423580657 A-to-I Human chr10 - 17614705 17614701 17614705 TTCCTTGTTATTTCCTTTTTTTTTCTTTTGTTAAGCCAAGCCCTTGCTCTGTTTTCCAGGCTGGA TTCCTTGTTATTTCCTTTTTTTTTCTTTTGTT____CAAGCCCTTGCTCTGTTTTCCAGGCTGGA GGCTT G HACD1 Ensembl:ENSG00000165996 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1554817830 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_2208753 RMVar_hsa_circ_115426,RMVar_hsa_circ_142467 36275 RMVar_ID_36275 Human_SNP_ID_423581006 A-to-I Human chr10 - 17615845 17615845 17615845 CTCCTGCCTCGGCCTCCGGAGTAGCTGGGACTACAAGCGTGGGCCACCACGCCCCATTAATTTTT CTCCTGCCTCGGCCTCCGGAGTAGCTGGGACTGCAAGCGTGGGCCACCACGCCCCATTAATTTTT T C HACD1 Ensembl:ENSG00000165996 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1420980702 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115426,RMVar_hsa_circ_142467 36276 RMVar_ID_36276 Human_SNP_ID_423601142 A-to-I Human chr10 + 17686454 17686454 17686454 GCTGGAGTACAGTGGCGTGATCTCAGCTGACTATAGCCTCTGCCTCCCGGGTTCAAGTGATTCTC GCTGGAGTACAGTGGCGTGATCTCAGCTGACTGTAGCCTCTGCCTCCCGGGTTCAAGTGATTCTC A G STAM Ensembl:ENSG00000136738 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs374258125 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16101,RMVar_hsa_circ_142470,RMVar_hsa_circ_79829,RMVar_hsa_circ_369370,RMVar_hsa_circ_43477,RMVar_hsa_circ_142472,RMVar_hsa_circ_327935,RMVar_hsa_circ_44936,RMVar_hsa_circ_79360,RMVar_hsa_circ_29795,RMVar_hsa_circ_142473 36277 RMVar_ID_36277 Human_SNP_ID_423601169 A-to-I Human chr10 + 17686522 17686522 17686522 CCTCAGCCTCCTGAGTAGCTGGGAATACAGGCATGCGCCACCACGCCTGGCTGGTTTTTGTAGTG CCTCAGCCTCCTGAGTAGCTGGGAATACAGGCGTGCGCCACCACGCCTGGCTGGTTTTTGTAGTG A G STAM Ensembl:ENSG00000136738 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1393797962 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16101,RMVar_hsa_circ_142470,RMVar_hsa_circ_79829,RMVar_hsa_circ_369370,RMVar_hsa_circ_43477,RMVar_hsa_circ_142472,RMVar_hsa_circ_327935,RMVar_hsa_circ_44936,RMVar_hsa_circ_79360,RMVar_hsa_circ_29795,RMVar_hsa_circ_142473 36278 RMVar_ID_36278 Human_SNP_ID_423601324 A-to-I Human chr10 + 17687219 17687219 17687219 ATTTTGGGCTGGGCACGGTGGCTCATGCCTGTAATCGCAGCACTTTGGGAGGCTGAGGCGGGCGA ATTTTGGGCTGGGCACGGTGGCTCATGCCTGTGATCGCAGCACTTTGGGAGGCTGAGGCGGGCGA A G STAM Ensembl:ENSG00000136738 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1487223796 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16101,RMVar_hsa_circ_142470,RMVar_hsa_circ_79829,RMVar_hsa_circ_369370,RMVar_hsa_circ_43477,RMVar_hsa_circ_142472,RMVar_hsa_circ_327935,RMVar_hsa_circ_44936,RMVar_hsa_circ_79360,RMVar_hsa_circ_29795,RMVar_hsa_circ_142473 36279 RMVar_ID_36279 Human_SNP_ID_423601367 A-to-I Human chr10 + 17687321 17687320 17687321 ACATGGTAAAACCCCGCGTCTGCTAAAAGTACAAAAATTAGCTGGGCATGGTGGTGCGCGCCTGT ACATGGTAAAACCCCGCGTCTGCTAAAAGTAC_AAAATTAGCTGGGCATGGTGGTGCGCGCCTGT CA C STAM Ensembl:ENSG00000136738 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs531063972 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_11324598 RMVar_hsa_circ_16101,RMVar_hsa_circ_142470,RMVar_hsa_circ_79829,RMVar_hsa_circ_369370,RMVar_hsa_circ_43477,RMVar_hsa_circ_142472,RMVar_hsa_circ_327935,RMVar_hsa_circ_44936,RMVar_hsa_circ_79360,RMVar_hsa_circ_29795,RMVar_hsa_circ_142473 36280 RMVar_ID_36280 Human_SNP_ID_423601372 A-to-I Human chr10 + 17687336 17687336 17687336 GCGTCTGCTAAAAGTACAAAAATTAGCTGGGCATGGTGGTGCGCGCCTGTAATCCTACTCGGGAG GCGTCTGCTAAAAGTACAAAAATTAGCTGGGCGTGGTGGTGCGCGCCTGTAATCCTACTCGGGAG A G STAM Ensembl:ENSG00000136738 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs375051606 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16101,RMVar_hsa_circ_142470,RMVar_hsa_circ_79829,RMVar_hsa_circ_369370,RMVar_hsa_circ_43477,RMVar_hsa_circ_142472,RMVar_hsa_circ_327935,RMVar_hsa_circ_44936,RMVar_hsa_circ_79360,RMVar_hsa_circ_29795,RMVar_hsa_circ_142473 36281 RMVar_ID_36281 Human_SNP_ID_423601393 A-to-I Human chr10 + 17687377 17687376 17687378 CGCGCCTGTAATCCTACTCGGGAGGTTGACACAAGAGAATCGCTTGAACCGCATCCCCCACCCCC CGCGCCTGTAATCCTACTCGGGAGGTTGACAC__GAGAATCGCTTGAACCGCATCCCCCACCCCC CAA C STAM Ensembl:ENSG00000136738 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1397561038 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_17558892,Human_RBP_ID_23304261 RMVar_hsa_circ_16101,RMVar_hsa_circ_142470,RMVar_hsa_circ_79829,RMVar_hsa_circ_369370,RMVar_hsa_circ_43477,RMVar_hsa_circ_142472,RMVar_hsa_circ_327935,RMVar_hsa_circ_44936,RMVar_hsa_circ_79360,RMVar_hsa_circ_29795,RMVar_hsa_circ_142473 36282 RMVar_ID_36282 Human_SNP_ID_423629628 A-to-I Human chr10 + 17797473 17797473 17797473 CTGCCACCACGCTGGCTAATTTTTGTATTTTTAGTAGAGACGAGGTTTCACCATGTTGGCCAGGC CTGCCACCACGCTGGCTAATTTTTGTATTTTTGGTAGAGACGAGGTTTCACCATGTTGGCCAGGC A G TMEM236 Ensembl:ENSG00000148483 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs929165426 Functional Loss SNV dbSNP153 33..33 33 - - - 36283 RMVar_ID_36283 Human_SNP_ID_423629629 A-to-I Human chr10 + 17797476 17797476 17797476 CCACCACGCTGGCTAATTTTTGTATTTTTAGTAGAGACGAGGTTTCACCATGTTGGCCAGGCTGG CCACCACGCTGGCTAATTTTTGTATTTTTAGTGGAGACGAGGTTTCACCATGTTGGCCAGGCTGG A G TMEM236 Ensembl:ENSG00000148483 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1046236549 Functional Loss SNV dbSNP153 33..33 33 - - - 36284 RMVar_ID_36284 Human_SNP_ID_423682796 A-to-I Human chr10 + 18013461 18013461 18013461 ATGATCATAGCTTACTGTAGGCTTGATCTCCTAGGATCAAGTGATTCTCCTACCTCAGCCTCCCA ATGATCATAGCTTACTGTAGGCTTGATCTCCTGGGATCAAGTGATTCTCCTACCTCAGCCTCCCA A G SLC39A12 Ensembl:ENSG00000148482 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982831049 Functional Loss SNV dbSNP153 33..33 33 - - - 36285 RMVar_ID_36285 Human_SNP_ID_423751507 A-to-I Human chr10 + 18257823 18257823 18257823 TGGAGTGCAGTGGCATGATCTCGGCTCACTGCAACCTCTGCCTCTCAGGTTCAAGCAATTCTCCT TGGAGTGCAGTGGCATGATCTCGGCTCACTGCCACCTCTGCCTCTCAGGTTCAAGCAATTCTCCT A C CACNB2 Ensembl:ENSG00000165995 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs572540766 Functional Loss SNV dbSNP153 33..33 33 - - - 36286 RMVar_ID_36286 Human_SNP_ID_423751518 A-to-I Human chr10 + 18257847 18257847 18257847 CTCACTGCAACCTCTGCCTCTCAGGTTCAAGCAATTCTCCTTCCTCAGCCTCCCGAGTAGCTGGG CTCACTGCAACCTCTGCCTCTCAGGTTCAAGCGATTCTCCTTCCTCAGCCTCCCGAGTAGCTGGG A G CACNB2 Ensembl:ENSG00000165995 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1251471685 Functional Loss SNV dbSNP153 33..33 33 - - - 36287 RMVar_ID_36287 Human_SNP_ID_423751730 A-to-I Human chr10 + 18258651 18258651 18258651 AGGAGCCTGAGGAAGGAGAATCACTTGAACCCAGGAGGTGGAGGTTGCAGTGAGCTGAGATCATG AGGAGCCTGAGGAAGGAGAATCACTTGAACCCGGGAGGTGGAGGTTGCAGTGAGCTGAGATCATG A G CACNB2 Ensembl:ENSG00000165995 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1357271746 Functional Loss SNV dbSNP153 33..33 33 - - - 36288 RMVar_ID_36288 Human_SNP_ID_423773480 A-to-I Human chr10 + 18338864 18338864 18338864 AGGTTCAAATGATCCTCCCAACTCAGCCTCCCAAGTAGCTGGGACCACAGGCACATGCCACCATG AGGTTCAAATGATCCTCCCAACTCAGCCTCCCGAGTAGCTGGGACCACAGGCACATGCCACCATG A G CACNB2 Ensembl:ENSG00000165995 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1230262205 Functional Loss SNV dbSNP153 33..33 33 - - - 36289 RMVar_ID_36289 Human_SNP_ID_423773508 A-to-I Human chr10 + 18338960 18338960 18338960 CGGGGTCTTCCTTTGTTGCCCAGGCTGGTTTCAAACTCCTGGGCTCAAATGATCCTCCCACCTCG CGGGGTCTTCCTTTGTTGCCCAGGCTGGTTTCGAACTCCTGGGCTCAAATGATCCTCCCACCTCG A G CACNB2 Ensembl:ENSG00000165995 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1413767367 Functional Loss SNV dbSNP153 33..33 33 - - - 36290 RMVar_ID_36290 Human_SNP_ID_423792069 A-to-I Human chr10 + 18405702 18405702 18405702 AGACTCAGCCAGGCACAATGGCTCATGCCTGTAATCCCAGCAATTTGGGAGGCCGAGGCGGGTGG AGACTCAGCCAGGCACAATGGCTCATGCCTGTGATCCCAGCAATTTGGGAGGCCGAGGCGGGTGG A G CACNB2 Ensembl:ENSG00000165995 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879029146 Functional Loss SNV dbSNP153 33..33 33 - - - 36291 RMVar_ID_36291 Human_SNP_ID_423793125 A-to-I Human chr10 + 18409201 18409201 18409201 TGCATCTGTAAGCCCAGCTATCCCAGAGGCTGAAGCAGGAGAATCACTTGAACCCGGAGGCGGAG TGCATCTGTAAGCCCAGCTATCCCAGAGGCTGGAGCAGGAGAATCACTTGAACCCGGAGGCGGAG A G CACNB2 Ensembl:ENSG00000165995 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1158700435 Functional Loss SNV dbSNP153 33..33 33 - - - 36292 RMVar_ID_36292 Human_SNP_ID_423793188 A-to-I Human chr10 + 18409327 18409326 18409328 TCTCCAGGAAAAAAAAAAAAAAAAGTAGAGACAAAGTCTCCTTATGTTGCCCAGCCTGGTCTTGA TCTCCAGGAAAAAAAAAAAAAAAAGTAGAGAC__AGTCTCCTTATGTTGCCCAGCCTGGTCTTGA CAA C CACNB2 Ensembl:ENSG00000165995 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs376208173 Functional Loss DEL dbSNP153 33..34 33 - - - 36293 RMVar_ID_36293 Human_SNP_ID_423799340 A-to-I Human chr10 + 18431100 18431100 18431100 AGCCTCCTGGGTTCAAGCAATCCTCTCACCTCAGTCTCCAGGGTAGCTGAGATACAGGAGTGTAC AGCCTCCTGGGTTCAAGCAATCCTCTCACCTCTGTCTCCAGGGTAGCTGAGATACAGGAGTGTAC A T CACNB2 Ensembl:ENSG00000165995 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs778759098 Functional Loss SNV dbSNP153 33..33 33 - - - 36294 RMVar_ID_36294 Human_SNP_ID_423799748 A-to-I Human chr10 + 18432571 18432571 18432571 AAAAACATTCCAGGCTGGGTGCAGTGACTTACACCTGTATTCCCAGCACTTTGGGAGGCCAGAGG AAAAACATTCCAGGCTGGGTGCAGTGACTTACCCCTGTATTCCCAGCACTTTGGGAGGCCAGAGG A C CACNB2 Ensembl:ENSG00000165995 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1242504113 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11326124 36295 RMVar_ID_36295 Human_SNP_ID_423802272 A-to-I Human chr10 + 18441764 18441764 18441764 TCAAGCCATCCTCCCACCTCAGCCTCCCAAGTAGCTGGGACTATAGGCATGCGCCACCACACCCA TCAAGCCATCCTCCCACCTCAGCCTCCCAAGTCGCTGGGACTATAGGCATGCGCCACCACACCCA A C CACNB2 Ensembl:ENSG00000165995 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049401079 Functional Loss SNV dbSNP153 33..33 33 - - - 36296 RMVar_ID_36296 Human_SNP_ID_423802273 A-to-I Human chr10 + 18441764 18441764 18441764 TCAAGCCATCCTCCCACCTCAGCCTCCCAAGTAGCTGGGACTATAGGCATGCGCCACCACACCCA TCAAGCCATCCTCCCACCTCAGCCTCCCAAGTGGCTGGGACTATAGGCATGCGCCACCACACCCA A G CACNB2 Ensembl:ENSG00000165995 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049401079 Functional Loss SNV dbSNP153 33..33 33 - - - 36297 RMVar_ID_36297 Human_SNP_ID_423804389 A-to-I Human chr10 + 18448011 18448011 18448011 GGGAAAGACACTTTCTTTTTGTTTTTTAATAGAGATAGGGTCTTGCTCTGTTGCCCAGGCTGGAG GGGAAAGACACTTTCTTTTTGTTTTTTAATAGGGATAGGGTCTTGCTCTGTTGCCCAGGCTGGAG A G CACNB2 Ensembl:ENSG00000165995 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs374476354 Functional Loss SNV dbSNP153 33..33 33 - - - 36298 RMVar_ID_36298 Human_SNP_ID_423808145 A-to-I Human chr10 + 18461175 18461175 18461175 TCCTTACCTGATCTGCACACCTCGGCCTCCCAAAGTGCTGGGAATACAGGCATGAGCCACTGCGC TCCTTACCTGATCTGCACACCTCGGCCTCCCACAGTGCTGGGAATACAGGCATGAGCCACTGCGC A C CACNB2 Ensembl:ENSG00000165995 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893544441 Functional Loss SNV dbSNP153 33..33 33 - - - 36299 RMVar_ID_36299 Human_SNP_ID_423808146 A-to-I Human chr10 + 18461175 18461175 18461175 TCCTTACCTGATCTGCACACCTCGGCCTCCCAAAGTGCTGGGAATACAGGCATGAGCCACTGCGC TCCTTACCTGATCTGCACACCTCGGCCTCCCATAGTGCTGGGAATACAGGCATGAGCCACTGCGC A T CACNB2 Ensembl:ENSG00000165995 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893544441 Functional Loss SNV dbSNP153 33..33 33 - - - 36300 RMVar_ID_36300 Human_SNP_ID_423809748 A-to-I Human chr10 + 18466284 18466284 18466284 TTTAGAGACAGTGTCGCTCTGTCACCCAGCCTAGAGTGCAGTGACATGATCATAGCTCACTGCAG TTTAGAGACAGTGTCGCTCTGTCACCCAGCCTGGAGTGCAGTGACATGATCATAGCTCACTGCAG A G CACNB2 Ensembl:ENSG00000165995 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1263174468 Functional Loss SNV dbSNP153 33..33 33 - - - 36301 RMVar_ID_36301 Human_SNP_ID_423809762 A-to-I Human chr10 + 18466315 18466315 18466315 TAGAGTGCAGTGACATGATCATAGCTCACTGCAGCCTCAAACTTCTGGACTGAAGCAACCCTCCA TAGAGTGCAGTGACATGATCATAGCTCACTGCGGCCTCAAACTTCTGGACTGAAGCAACCCTCCA A G CACNB2 Ensembl:ENSG00000165995 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1400656098 Functional Loss SNV dbSNP153 33..33 33 - - - 36302 RMVar_ID_36302 Human_SNP_ID_423810383 A-to-I Human chr10 + 18468350 18468350 18468350 AGGCATAGTGGCATGCATATGTAGTTTCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAG AGGCATAGTGGCATGCATATGTAGTTTCAGCTGCTTGGGAGGCTGAGGCAGGAGAATCGCTTGAG A G CACNB2 Ensembl:ENSG00000165995 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs912223433 Functional Loss SNV dbSNP153 33..33 33 - - - 36303 RMVar_ID_36303 Human_SNP_ID_423816282 A-to-I Human chr10 + 18487989 18487989 18487989 AGGGAATAAAAAGTCATGCAAATTGTACTTTTAGTAGAGACAGGGTTTCACCATGTTGCACTGGC AGGGAATAAAAAGTCATGCAAATTGTACTTTTGGTAGAGACAGGGTTTCACCATGTTGCACTGGC A G CACNB2 Ensembl:ENSG00000165995 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913174250 Functional Loss SNV dbSNP153 33..33 33 - - - 36304 RMVar_ID_36304 Human_SNP_ID_423816289 A-to-I Human chr10 + 18488009 18488009 18488009 AATTGTACTTTTAGTAGAGACAGGGTTTCACCATGTTGCACTGGCTGGTCTCGAACTCCTGACCT AATTGTACTTTTAGTAGAGACAGGGTTTCACCGTGTTGCACTGGCTGGTCTCGAACTCCTGACCT A G CACNB2 Ensembl:ENSG00000165995 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913591768 Functional Loss SNV dbSNP153 33..33 33 - - - 36305 RMVar_ID_36305 Human_SNP_ID_423831418 A-to-I Human chr10 - 18537201 18537201 18537201 GATGGATCACTTGAGGTCGGGAGTTTGAGACCAGCCTGGGCAACATGGCAAAGCCCCGTCTCTAC GATGGATCACTTGAGGTCGGGAGTTTGAGACCGGCCTGGGCAACATGGCAAAGCCCCGTCTCTAC T C AL450384.2 Ensembl:ENSG00000240291 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1312743682 Functional Loss SNV dbSNP153 33..33 33 - - - 36306 RMVar_ID_36306 Human_SNP_ID_423831543 A-to-I Human chr10 - 18537701 18537701 18537701 CTGATCTTGGTTCAGTGCAACCTTGGCCTCCCAGGTTCAAGTGATTTTCCTGCCTCAGCTTCTCA CTGATCTTGGTTCAGTGCAACCTTGGCCTCCCTGGTTCAAGTGATTTTCCTGCCTCAGCTTCTCA T A AL450384.2 Ensembl:ENSG00000240291 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909767416 Functional Loss SNV dbSNP153 33..33 33 - - - 36307 RMVar_ID_36307 Human_SNP_ID_423841362 A-to-I Human chr10 - 18564230 18564230 18564230 GTATGGGAATGGAATGGAGAATGGAATGTAATAGAGAGTGGATGGAATGTATTACAGTGGAGAAT GTATGGGAATGGAATGGAGAATGGAATGTAATGGAGAGTGGATGGAATGTATTACAGTGGAGAAT T C NSUN6 Ensembl:ENSG00000241058 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1008196569 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_191788 RMVar_hsa_circ_75180,RMVar_hsa_circ_110674,RMVar_hsa_circ_265392,RMVar_hsa_circ_142500,RMVar_hsa_circ_5757,RMVar_hsa_circ_53695 36308 RMVar_ID_36308 Human_SNP_ID_423856518 A-to-I Human chr10 - 18612163 18612163 18612163 TCTCCACCTTGGCCTCCCAAAGTGCTAAGATTATAGGGATGAGACGCCACACCCAGCCAGGACTG TCTCCACCTTGGCCTCCCAAAGTGCTAAGATTGTAGGGATGAGACGCCACACCCAGCCAGGACTG T C NSUN6 Ensembl:ENSG00000241058 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334985431 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75180,RMVar_hsa_circ_265392,RMVar_hsa_circ_304992,RMVar_hsa_circ_5757,RMVar_hsa_circ_53695,RMVar_hsa_circ_353618,RMVar_hsa_circ_367694,RMVar_hsa_circ_313309,RMVar_hsa_circ_267252,RMVar_hsa_circ_291385,RMVar_hsa_circ_142510,RMVar_hsa_circ_66098,RMVar_hsa_circ_142503,RMVar_hsa_circ_142504,RMVar_hsa_circ_142505,RMVar_hsa_circ_142502,RMVar_hsa_circ_288267,RMVar_hsa_circ_349050,RMVar_hsa_circ_350759,RMVar_hsa_circ_294757,RMVar_hsa_circ_322762,RMVar_hsa_circ_142506,RMVar_hsa_circ_142507,RMVar_hsa_circ_357701,RMVar_hsa_circ_365539,RMVar_hsa_circ_341950,RMVar_hsa_circ_269832,RMVar_hsa_circ_142511 36309 RMVar_ID_36309 Human_SNP_ID_423866356 A-to-I Human chr10 - 18642015 18642015 18642015 TTACCCAGGCTGGAGTGCAGGGACACAAGCATAGCTCATTGCAGGCTCGAACTTCTGGACTCAGG TTACCCAGGCTGGAGTGCAGGGACACAAGCATGGCTCATTGCAGGCTCGAACTTCTGGACTCAGG T C NSUN6 Ensembl:ENSG00000241058 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs561208820 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24798277 RMVar_hsa_circ_75180,RMVar_hsa_circ_304992,RMVar_hsa_circ_53695,RMVar_hsa_circ_353618,RMVar_hsa_circ_367694,RMVar_hsa_circ_291385,RMVar_hsa_circ_66098,RMVar_hsa_circ_142504,RMVar_hsa_circ_142505,RMVar_hsa_circ_349050,RMVar_hsa_circ_350759,RMVar_hsa_circ_294757,RMVar_hsa_circ_322762,RMVar_hsa_circ_142506,RMVar_hsa_circ_357701,RMVar_hsa_circ_365539,RMVar_hsa_circ_341950,RMVar_hsa_circ_142511,RMVar_hsa_circ_58889,RMVar_hsa_circ_360438,RMVar_hsa_circ_365283,RMVar_hsa_circ_359851 36310 RMVar_ID_36310 Human_SNP_ID_423867574 A-to-I Human chr10 - 18646032 18646032 18646032 CGCCACAATGCTCGGCTAATTTTGATATTCTTAGCACAGATGGGATTTCACCATGTTGGCCAGGC CGCCACAATGCTCGGCTAATTTTGATATTCTTGGCACAGATGGGATTTCACCATGTTGGCCAGGC T C NSUN6 Ensembl:ENSG00000241058 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1378209423 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75180,RMVar_hsa_circ_53695,RMVar_hsa_circ_353618,RMVar_hsa_circ_291385,RMVar_hsa_circ_142505,RMVar_hsa_circ_349050,RMVar_hsa_circ_350759,RMVar_hsa_circ_357701,RMVar_hsa_circ_341950,RMVar_hsa_circ_58889,RMVar_hsa_circ_360438,RMVar_hsa_circ_365283,RMVar_hsa_circ_290333,RMVar_hsa_circ_366855,RMVar_hsa_circ_142514 36311 RMVar_ID_36311 Human_SNP_ID_423870057 A-to-I Human chr10 - 18654620 18654620 18654620 CCTCAGCCTCCCAAAGTGTTGGGATTACAGGCATGAGCCACTGCGCCAGGCCACTTTCCAGATAC CCTCAGCCTCCCAAAGTGTTGGGATTACAGGCCTGAGCCACTGCGCCAGGCCACTTTCCAGATAC T G NSUN6 Ensembl:ENSG00000241058 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1013598258 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_53695,RMVar_hsa_circ_291385,RMVar_hsa_circ_142505,RMVar_hsa_circ_350759,RMVar_hsa_circ_341950,RMVar_hsa_circ_360438,RMVar_hsa_circ_366855,RMVar_hsa_circ_312870 36312 RMVar_ID_36312 Human_SNP_ID_423870058 A-to-I Human chr10 - 18654626 18654626 18654626 CACCCGCCTCAGCCTCCCAAAGTGTTGGGATTACAGGCATGAGCCACTGCGCCAGGCCACTTTCC CACCCGCCTCAGCCTCCCAAAGTGTTGGGATTTCAGGCATGAGCCACTGCGCCAGGCCACTTTCC T A NSUN6 Ensembl:ENSG00000241058 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs751167361 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_53695,RMVar_hsa_circ_291385,RMVar_hsa_circ_142505,RMVar_hsa_circ_350759,RMVar_hsa_circ_341950,RMVar_hsa_circ_360438,RMVar_hsa_circ_366855,RMVar_hsa_circ_312870 36313 RMVar_ID_36313 Human_SNP_ID_423870082 A-to-I Human chr10 - 18654732 18654732 18654732 GGGACTACAGGCACGTGCCATCACGCCAGGCTAATTTTTGCATTTTTAGTACAGATGGGGTTTTA GGGACTACAGGCACGTGCCATCACGCCAGGCTGATTTTTGCATTTTTAGTACAGATGGGGTTTTA T C NSUN6 Ensembl:ENSG00000241058 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1269172784 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_53695,RMVar_hsa_circ_291385,RMVar_hsa_circ_142505,RMVar_hsa_circ_350759,RMVar_hsa_circ_341950,RMVar_hsa_circ_360438,RMVar_hsa_circ_366855,RMVar_hsa_circ_312870 36314 RMVar_ID_36314 Human_SNP_ID_423870672 A-to-I Human chr10 - 18657003 18657001 18657003 GACAACATGGAGAAATCCTGTCTCTCCAAAAAAATACAAAAGTTAGCTGGACATGGTGGTGCACA GACAACATGGAGAAATCCTGTCTCTCCAAAAA__TACAAAAGTTAGCTGGACATGGTGGTGCACA ATT A NSUN6 Ensembl:ENSG00000241058 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs962762328 Functional Loss DEL dbSNP153 33..34 33 - - - 36315 RMVar_ID_36315 Human_SNP_ID_423870673 A-to-I Human chr10 - 18657003 18657001 18657003 GACAACATGGAGAAATCCTGTCTCTCCAAAAAAATACAAAAGTTAGCTGGACATGGTGGTGCACA GACAACATGGAGAAATCCTGTCTCTCCAAAAA_ATACAAAAGTTAGCTGGACATGGTGGTGCACA ATT AT NSUN6 Ensembl:ENSG00000241058 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs962762328 Functional Loss DEL dbSNP153 33..33 33 - - - 36316 RMVar_ID_36316 Human_SNP_ID_423874712 A-to-I Human chr10 + 18669846 18669846 18669846 AAACCCCGTCTCTACTAAAAATACAAAAAACTAGCCGGGCGTGGTGGGGCAGACTTGTAGTCCCC AAACCCCGTCTCTACTAAAAATACAAAAAACTGGCCGGGCGTGGTGGGGCAGACTTGTAGTCCCC A G ARL5B Ensembl:ENSG00000165997 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs561842660 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20905,RMVar_hsa_circ_64507 36317 RMVar_ID_36317 Human_SNP_ID_423874725 A-to-I Human chr10 + 18669872 18669872 18669872 AAAACTAGCCGGGCGTGGTGGGGCAGACTTGTAGTCCCCAGCTACTCAGGAGGCTGAGGCAGGAG AAAACTAGCCGGGCGTGGTGGGGCAGACTTGTTGTCCCCAGCTACTCAGGAGGCTGAGGCAGGAG A T ARL5B Ensembl:ENSG00000165997 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1439457995 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20905,RMVar_hsa_circ_64507 36318 RMVar_ID_36318 Human_SNP_ID_424209544 A-to-I Human chr10 + 19846912 19846912 19846912 CCATATGGCTGAGGAGGTGTCACAATCATGGCAGAAGGGAAAAGGCACGTCTTACACGGCAGCGG CCATATGGCTGAGGAGGTGTCACAATCATGGCGGAAGGGAAAAGGCACGTCTTACACGGCAGCGG A G PLXDC2 Ensembl:ENSG00000120594 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs550777368 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82532,RMVar_hsa_circ_142528 36319 RMVar_ID_36319 Human_SNP_ID_424209545 A-to-I Human chr10 + 19846921 19846921 19846921 TGAGGAGGTGTCACAATCATGGCAGAAGGGAAAAGGCACGTCTTACACGGCAGCGGGCAAGAGAG TGAGGAGGTGTCACAATCATGGCAGAAGGGAAGAGGCACGTCTTACACGGCAGCGGGCAAGAGAG A G PLXDC2 Ensembl:ENSG00000120594 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs72784112 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_4044 RMVar_hsa_circ_82532,RMVar_hsa_circ_142528 36320 RMVar_ID_36320 Human_SNP_ID_424232299 A-to-I Human chr10 + 19930792 19930792 19930792 CAAGGCCAGCCTGACCAACAAGGTGAAATCCCATCTCTACTAAAACTACAAAAATTAGCCAGGCC CAAGGCCAGCCTGACCAACAAGGTGAAATCCCGTCTCTACTAAAACTACAAAAATTAGCCAGGCC A G PLXDC2 Ensembl:ENSG00000120594 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1322662253 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82532,RMVar_hsa_circ_142528 36321 RMVar_ID_36321 Human_SNP_ID_424232302 A-to-I Human chr10 + 19930820 19930820 19930820 TCCCATCTCTACTAAAACTACAAAAATTAGCCAGGCCTGGTTGCAGGTGCTTGCAATCCCAGCTA TCCCATCTCTACTAAAACTACAAAAATTAGCCGGGCCTGGTTGCAGGTGCTTGCAATCCCAGCTA A G PLXDC2 Ensembl:ENSG00000120594 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs887627012 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82532,RMVar_hsa_circ_142528 36322 RMVar_ID_36322 Human_SNP_ID_424327173 A-to-I Human chr10 + 20286764 20286764 20286764 GTTGTTGTTTGAGATGGGGTTTTGCTCTTGTTACCCAGGCTGGAGTGCAATGGCGTGATCTCGTC GTTGTTGTTTGAGATGGGGTTTTGCTCTTGTTGCCCAGGCTGGAGTGCAATGGCGTGATCTCGTC A G PLXDC2 Ensembl:ENSG00000120594 Protein coding 3'UTR GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1304760663 Functional Loss SNV dbSNP153 33..33 33 - - - 36323 RMVar_ID_36323 Human_SNP_ID_424327187 A-to-I Human chr10 + 20286804 20286804 20286804 TGGAGTGCAATGGCGTGATCTCGTCTCACTGCAACCTCCGCCTCCCAGGTTCAAGCGATTCTCCT TGGAGTGCAATGGCGTGATCTCGTCTCACTGCCACCTCCGCCTCCCAGGTTCAAGCGATTCTCCT A C PLXDC2 Ensembl:ENSG00000120594 Protein coding 3'UTR GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs767562953 Functional Loss SNV dbSNP153 33..33 33 - - - 36324 RMVar_ID_36324 Human_SNP_ID_424327188 A-to-I Human chr10 + 20286804 20286804 20286804 TGGAGTGCAATGGCGTGATCTCGTCTCACTGCAACCTCCGCCTCCCAGGTTCAAGCGATTCTCCT TGGAGTGCAATGGCGTGATCTCGTCTCACTGCGACCTCCGCCTCCCAGGTTCAAGCGATTCTCCT A G PLXDC2 Ensembl:ENSG00000120594 Protein coding 3'UTR GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs767562953 Functional Loss SNV dbSNP153 33..33 33 - - - 36325 RMVar_ID_36325 Human_SNP_ID_424505555 A-to-I Human chr10 - 20913008 20913008 20913008 CCTGTAATATGAGTACTTTGGGAGGCTGAGACAGGAGGATCATTTGAGGCCAGGAGCTTGAAACC CCTGTAATATGAGTACTTTGGGAGGCTGAGACGGGAGGATCATTTGAGGCCAGGAGCTTGAAACC T C NEBL Ensembl:ENSG00000078114 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1449677147 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77257,RMVar_hsa_circ_142546,RMVar_hsa_circ_114047,RMVar_hsa_circ_142548,RMVar_hsa_circ_142567,RMVar_hsa_circ_142566,RMVar_hsa_circ_142572,RMVar_hsa_circ_142571 36326 RMVar_ID_36326 Human_SNP_ID_424563740 A-to-I Human chr10 - 21136466 21136466 21136466 AAAAGGGCTGGGCATGGTGGCCCATGCCTGTTATCTCAGCCCTTTGGGAGGCTGAGGTGAGAGGA AAAAGGGCTGGGCATGGTGGCCCATGCCTGTTGTCTCAGCCCTTTGGGAGGCTGAGGTGAGAGGA T C NEBL,C10orf113 Ensembl:ENSG00000078114,Ensembl:ENSG00000204683 Protein coding,Protein coding intron,intron GSE107867 ASD brains,cerebellum;ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs558481607 Functional Loss SNV dbSNP153 33..33 33 - - - 36327 RMVar_ID_36327 Human_SNP_ID_424564013 A-to-I Human chr10 - 21137715 21137715 21137715 TTGCCCAGGCTGGTTTCAAACTGCTGGCCTGAAGCAATCCTTCTGCTTCAGCCTCCCAAAGTGCT TTGCCCAGGCTGGTTTCAAACTGCTGGCCTGAGGCAATCCTTCTGCTTCAGCCTCCCAAAGTGCT T C NEBL,C10orf113 Ensembl:ENSG00000078114,Ensembl:ENSG00000204683 Protein coding,Protein coding intron,intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1456180858 Functional Loss SNV dbSNP153 33..33 33 - - - 36328 RMVar_ID_36328 Human_SNP_ID_424566778 A-to-I Human chr10 - 21148608 21148608 21148608 GGCAGGCCAATCGCTTCCACGCAGGAGGTGGAAGTTGCAGTGAGCTGAGATCACGCCACTGCACT GGCAGGCCAATCGCTTCCACGCAGGAGGTGGAGGTTGCAGTGAGCTGAGATCACGCCACTGCACT T C NEBL Ensembl:ENSG00000078114 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1039759516 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_142575 36329 RMVar_ID_36329 Human_SNP_ID_424656172 A-to-I Human chr10 - 21486808 21486808 21486808 TGGCTCACCACAAACTCTGCCTCCCGGGTCCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCT TGGCTCACCACAAACTCTGCCTCCCGGGTCCAGGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs536335704 Functional Loss SNV dbSNP153 33..33 33 - - - 36330 RMVar_ID_36330 Human_SNP_ID_424656173 A-to-I Human chr10 - 21486808 21486808 21486808 TGGCTCACCACAAACTCTGCCTCCCGGGTCCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCT TGGCTCACCACAAACTCTGCCTCCCGGGTCCACGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCT T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs536335704 Functional Loss SNV dbSNP153 33..33 33 - - - 36331 RMVar_ID_36331 Human_SNP_ID_424670911 A-to-I Human chr10 + 21540133 21540133 21540133 TTAGTTGGGGCTGGGCACAGTGGCTCATGCCTATAATTCCAGCACTTTGGTAGGCTGAGGTGGGC TTAGTTGGGGCTGGGCACAGTGGCTCATGCCTGTAATTCCAGCACTTTGGTAGGCTGAGGTGGGC A G MLLT10 Ensembl:ENSG00000078403 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1013287454 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24798712 RMVar_hsa_circ_22163,RMVar_hsa_circ_41652,RMVar_hsa_circ_119150,RMVar_hsa_circ_142578,RMVar_hsa_circ_97333,RMVar_hsa_circ_343303,RMVar_hsa_circ_361775,RMVar_hsa_circ_368909,RMVar_hsa_circ_349944,RMVar_hsa_circ_335552,RMVar_hsa_circ_60387,RMVar_hsa_circ_142579,RMVar_hsa_circ_142580 36332 RMVar_ID_36332 Human_SNP_ID_424671310 A-to-I Human chr10 + 21541503 21541503 21541503 TGCCTCCTGGATTCAAACGATTCTCCTGCCTCAGTCTCCCATGTATCTGGGACTACAGACATGCG TGCCTCCTGGATTCAAACGATTCTCCTGCCTCGGTCTCCCATGTATCTGGGACTACAGACATGCG A G MLLT10 Ensembl:ENSG00000078403 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1008308161 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22163,RMVar_hsa_circ_41652,RMVar_hsa_circ_119150,RMVar_hsa_circ_142578,RMVar_hsa_circ_97333,RMVar_hsa_circ_343303,RMVar_hsa_circ_361775,RMVar_hsa_circ_368909,RMVar_hsa_circ_349944,RMVar_hsa_circ_335552,RMVar_hsa_circ_60387,RMVar_hsa_circ_142579,RMVar_hsa_circ_142580 36333 RMVar_ID_36333 Human_SNP_ID_424671387 A-to-I Human chr10 + 21541748 21541748 21541748 GTTGACCAGCCTCGTCTGGAATTCCTGAGCTCAAGCAGTCCTCCTACCTCAGCCTCCCAAAGTGG GTTGACCAGCCTCGTCTGGAATTCCTGAGCTCGAGCAGTCCTCCTACCTCAGCCTCCCAAAGTGG A G MLLT10 Ensembl:ENSG00000078403 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs536742802 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22163,RMVar_hsa_circ_41652,RMVar_hsa_circ_119150,RMVar_hsa_circ_142578,RMVar_hsa_circ_97333,RMVar_hsa_circ_343303,RMVar_hsa_circ_361775,RMVar_hsa_circ_368909,RMVar_hsa_circ_349944,RMVar_hsa_circ_335552,RMVar_hsa_circ_60387,RMVar_hsa_circ_142579,RMVar_hsa_circ_142580 36334 RMVar_ID_36334 Human_SNP_ID_424687548 A-to-I Human chr10 + 21601013 21601013 21601013 TTGCCCAGCCTGGAGTGCAGTGGTGCAATTACAGCTCACTGTAGCTTCTACTTCCCAGCCTCAAG TTGCCCAGCCTGGAGTGCAGTGGTGCAATTACCGCTCACTGTAGCTTCTACTTCCCAGCCTCAAG A C MLLT10 Ensembl:ENSG00000078403 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1235255555 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2210591,Human_RBP_ID_11330927 RMVar_hsa_circ_6168,RMVar_hsa_circ_20632,RMVar_hsa_circ_119150,RMVar_hsa_circ_142578,RMVar_hsa_circ_97333,RMVar_hsa_circ_343303,RMVar_hsa_circ_361775,RMVar_hsa_circ_368909,RMVar_hsa_circ_349944,RMVar_hsa_circ_60387,RMVar_hsa_circ_142579,RMVar_hsa_circ_332013,RMVar_hsa_circ_58350,RMVar_hsa_circ_19036,RMVar_hsa_circ_283296,RMVar_hsa_circ_348707,RMVar_hsa_circ_350854,RMVar_hsa_circ_318060,RMVar_hsa_circ_65582,RMVar_hsa_circ_13059,RMVar_hsa_circ_142583,RMVar_hsa_circ_288611,RMVar_hsa_circ_357167,RMVar_hsa_circ_359464,RMVar_hsa_circ_58461,RMVar_hsa_circ_142584 36335 RMVar_ID_36335 Human_SNP_ID_424687556 A-to-I Human chr10 + 21601030 21601030 21601030 CAGTGGTGCAATTACAGCTCACTGTAGCTTCTACTTCCCAGCCTCAAGCAATCCTCCCATCTCAG CAGTGGTGCAATTACAGCTCACTGTAGCTTCTGCTTCCCAGCCTCAAGCAATCCTCCCATCTCAG A G MLLT10 Ensembl:ENSG00000078403 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350024338 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2210591,Human_RBP_ID_11330927 RMVar_hsa_circ_6168,RMVar_hsa_circ_20632,RMVar_hsa_circ_119150,RMVar_hsa_circ_142578,RMVar_hsa_circ_97333,RMVar_hsa_circ_343303,RMVar_hsa_circ_361775,RMVar_hsa_circ_368909,RMVar_hsa_circ_349944,RMVar_hsa_circ_60387,RMVar_hsa_circ_142579,RMVar_hsa_circ_332013,RMVar_hsa_circ_58350,RMVar_hsa_circ_19036,RMVar_hsa_circ_283296,RMVar_hsa_circ_348707,RMVar_hsa_circ_350854,RMVar_hsa_circ_318060,RMVar_hsa_circ_65582,RMVar_hsa_circ_13059,RMVar_hsa_circ_142583,RMVar_hsa_circ_288611,RMVar_hsa_circ_357167,RMVar_hsa_circ_359464,RMVar_hsa_circ_58461,RMVar_hsa_circ_142584 36336 RMVar_ID_36336 Human_SNP_ID_424687582 A-to-I Human chr10 + 21601146 21601146 21601146 TGTTTTATTTTTTATAGAGATAGGATCTCACTATGTTGCCTAGGCTGGTCTTGAACTCTTGGATT TGTTTTATTTTTTATAGAGATAGGATCTCACTGTGTTGCCTAGGCTGGTCTTGAACTCTTGGATT A G MLLT10 Ensembl:ENSG00000078403 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1244485531 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11330933 RMVar_hsa_circ_6168,RMVar_hsa_circ_20632,RMVar_hsa_circ_119150,RMVar_hsa_circ_142578,RMVar_hsa_circ_97333,RMVar_hsa_circ_343303,RMVar_hsa_circ_361775,RMVar_hsa_circ_368909,RMVar_hsa_circ_349944,RMVar_hsa_circ_60387,RMVar_hsa_circ_142579,RMVar_hsa_circ_332013,RMVar_hsa_circ_58350,RMVar_hsa_circ_19036,RMVar_hsa_circ_283296,RMVar_hsa_circ_348707,RMVar_hsa_circ_350854,RMVar_hsa_circ_318060,RMVar_hsa_circ_65582,RMVar_hsa_circ_13059,RMVar_hsa_circ_142583,RMVar_hsa_circ_288611,RMVar_hsa_circ_357167,RMVar_hsa_circ_359464,RMVar_hsa_circ_58461,RMVar_hsa_circ_142584 36337 RMVar_ID_36337 Human_SNP_ID_424689000 A-to-I Human chr10 + 21607001 21607001 21607001 ATTGTTATAAATGGCTGGGTGTGGTAGTTCACACCTTTAATCCCAGCCCTTTTGGAGACAGTAGG ATTGTTATAAATGGCTGGGTGTGGTAGTTCACGCCTTTAATCCCAGCCCTTTTGGAGACAGTAGG A G MLLT10 Ensembl:ENSG00000078403 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170311524 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3345984,Human_RBP_ID_8331711,Human_RBP_ID_11331101 RMVar_hsa_circ_6168,RMVar_hsa_circ_20632,RMVar_hsa_circ_119150,RMVar_hsa_circ_142578,RMVar_hsa_circ_97333,RMVar_hsa_circ_343303,RMVar_hsa_circ_361775,RMVar_hsa_circ_368909,RMVar_hsa_circ_349944,RMVar_hsa_circ_60387,RMVar_hsa_circ_142579,RMVar_hsa_circ_332013,RMVar_hsa_circ_58350,RMVar_hsa_circ_19036,RMVar_hsa_circ_283296,RMVar_hsa_circ_348707,RMVar_hsa_circ_350854,RMVar_hsa_circ_318060,RMVar_hsa_circ_65582,RMVar_hsa_circ_13059,RMVar_hsa_circ_142583,RMVar_hsa_circ_288611,RMVar_hsa_circ_357167,RMVar_hsa_circ_359464,RMVar_hsa_circ_58461,RMVar_hsa_circ_142584 36338 RMVar_ID_36338 Human_SNP_ID_424700332 A-to-I Human chr10 + 21650276 21650276 21650276 GGGAGGCTGAGGTGAGAGGATTGCTGGAGCCTAGGAGGTTGAGGCTGTAGTGAGCTGTGATCGTA GGGAGGCTGAGGTGAGAGGATTGCTGGAGCCTGGGAGGTTGAGGCTGTAGTGAGCTGTGATCGTA A G MLLT10 Ensembl:ENSG00000078403 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1190081080 Functional Loss SNV dbSNP153 33..33 33 - - - 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,RMVar_hsa_circ_142589 36339 RMVar_ID_36339 Human_SNP_ID_424702634 A-to-I Human chr10 + 21659530 21659530 21659530 TTCTTACTCTTAATCTTTTTTTTTTTTTTTTGAGACGGATTCTCGCTTTGTTGGCAGGGTTGGAG TTCTTACTCTTAATCTTTTTTTTTTTTTTTTGTGACGGATTCTCGCTTTGTTGGCAGGGTTGGAG A T MLLT10 Ensembl:ENSG00000078403 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1234325642 Functional Loss SNV dbSNP153 33..33 33 - - - 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 36340 RMVar_ID_36340 Human_SNP_ID_424702647 A-to-I Human chr10 + 21659585 21659585 21659585 AGGGTTGGAGTGCAGTGGTGTGATCTCGGCTCACTGCAGTCTTTGCCTCCTGGGTTCAAGGGATT AGGGTTGGAGTGCAGTGGTGTGATCTCGGCTCTCTGCAGTCTTTGCCTCCTGGGTTCAAGGGATT A T MLLT10 Ensembl:ENSG00000078403 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1418367812 Functional Loss SNV dbSNP153 33..33 33 - - - 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 36341 RMVar_ID_36341 Human_SNP_ID_424704540 A-to-I Human chr10 + 21666454 21666454 21666454 TTGGGAGGCCGAAGCGGGTGGATCACGAGGTCAAGAGATCAAGACCATCCTGCCCAACATGGTGA TTGGGAGGCCGAAGCGGGTGGATCACGAGGTCGAGAGATCAAGACCATCCTGCCCAACATGGTGA A G MLLT10 Ensembl:ENSG00000078403 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1209500929 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24799383 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 36342 RMVar_ID_36342 Human_SNP_ID_424704543 A-to-I Human chr10 + 21666462 21666462 21666462 CCGAAGCGGGTGGATCACGAGGTCAAGAGATCAAGACCATCCTGCCCAACATGGTGAAACCGCTC CCGAAGCGGGTGGATCACGAGGTCAAGAGATCCAGACCATCCTGCCCAACATGGTGAAACCGCTC A C MLLT10 Ensembl:ENSG00000078403 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs931331938 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24799383 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 36343 RMVar_ID_36343 Human_SNP_ID_424705845 A-to-I Human chr10 + 21671226 21671226 21671226 TTTTAGTAGAGATGGGATTTCACATGTTGGCCAGGCTGGTCTCGAACTGCTGATCTCAGGTGATC TTTTAGTAGAGATGGGATTTCACATGTTGGCCCGGCTGGTCTCGAACTGCTGATCTCAGGTGATC A C MLLT10 Ensembl:ENSG00000078403 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs920841422 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119150,RMVar_hsa_circ_142578,RMVar_hsa_circ_97333,RMVar_hsa_circ_60387,RMVar_hsa_circ_142579,RMVar_hsa_circ_58350,RMVar_hsa_circ_19036,RMVar_hsa_circ_65582,RMVar_hsa_circ_13059,RMVar_hsa_circ_58461,RMVar_hsa_circ_5456,RMVar_hsa_circ_109009,RMVar_hsa_circ_142586,RMVar_hsa_circ_327839,RMVar_hsa_circ_61898,RMVar_hsa_circ_65965,RMVar_hsa_circ_374784,RMVar_hsa_circ_75084,RMVar_hsa_circ_25936,RMVar_hsa_circ_71054,RMVar_hsa_circ_36195,RMVar_hsa_circ_142590,RMVar_hsa_circ_39526,RMVar_hsa_circ_29174,RMVar_hsa_circ_351722,RMVar_hsa_circ_361899,RMVar_hsa_circ_280539,RMVar_hsa_circ_142595 36344 RMVar_ID_36344 Human_SNP_ID_424705846 A-to-I Human chr10 + 21671226 21671226 21671226 TTTTAGTAGAGATGGGATTTCACATGTTGGCCAGGCTGGTCTCGAACTGCTGATCTCAGGTGATC TTTTAGTAGAGATGGGATTTCACATGTTGGCCGGGCTGGTCTCGAACTGCTGATCTCAGGTGATC A G MLLT10 Ensembl:ENSG00000078403 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs920841422 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119150,RMVar_hsa_circ_142578,RMVar_hsa_circ_97333,RMVar_hsa_circ_60387,RMVar_hsa_circ_142579,RMVar_hsa_circ_58350,RMVar_hsa_circ_19036,RMVar_hsa_circ_65582,RMVar_hsa_circ_13059,RMVar_hsa_circ_58461,RMVar_hsa_circ_5456,RMVar_hsa_circ_109009,RMVar_hsa_circ_142586,RMVar_hsa_circ_327839,RMVar_hsa_circ_61898,RMVar_hsa_circ_65965,RMVar_hsa_circ_374784,RMVar_hsa_circ_75084,RMVar_hsa_circ_25936,RMVar_hsa_circ_71054,RMVar_hsa_circ_36195,RMVar_hsa_circ_142590,RMVar_hsa_circ_39526,RMVar_hsa_circ_29174,RMVar_hsa_circ_351722,RMVar_hsa_circ_361899,RMVar_hsa_circ_280539,RMVar_hsa_circ_142595 36345 RMVar_ID_36345 Human_SNP_ID_424705893 A-to-I Human chr10 + 21671398 21671398 21671398 TTAAGGTTGGCCGGGCGTGGTGGCTCACATCTATAATCCTAGCAGTTTGGGATGCTGAGGTGGGC TTAAGGTTGGCCGGGCGTGGTGGCTCACATCTGTAATCCTAGCAGTTTGGGATGCTGAGGTGGGC A G MLLT10 Ensembl:ENSG00000078403 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277277352 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17558908 RMVar_hsa_circ_119150,RMVar_hsa_circ_142578,RMVar_hsa_circ_97333,RMVar_hsa_circ_60387,RMVar_hsa_circ_142579,RMVar_hsa_circ_58350,RMVar_hsa_circ_19036,RMVar_hsa_circ_65582,RMVar_hsa_circ_13059,RMVar_hsa_circ_58461,RMVar_hsa_circ_5456,RMVar_hsa_circ_109009,RMVar_hsa_circ_142586,RMVar_hsa_circ_327839,RMVar_hsa_circ_61898,RMVar_hsa_circ_65965,RMVar_hsa_circ_374784,RMVar_hsa_circ_75084,RMVar_hsa_circ_25936,RMVar_hsa_circ_71054,RMVar_hsa_circ_36195,RMVar_hsa_circ_142590,RMVar_hsa_circ_39526,RMVar_hsa_circ_29174,RMVar_hsa_circ_351722,RMVar_hsa_circ_361899,RMVar_hsa_circ_280539,RMVar_hsa_circ_142595 36346 RMVar_ID_36346 Human_SNP_ID_424705932 A-to-I Human chr10 + 21671595 21671595 21671595 ATCATCTGAGTTTAGGAGTTGGAGACCAGCCTAGGCAACATGGCAAAACCCTGTCTCTCTAAAAA ATCATCTGAGTTTAGGAGTTGGAGACCAGCCTCGGCAACATGGCAAAACCCTGTCTCTCTAAAAA A C MLLT10 Ensembl:ENSG00000078403 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs895214847 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119150,RMVar_hsa_circ_142578,RMVar_hsa_circ_97333,RMVar_hsa_circ_60387,RMVar_hsa_circ_142579,RMVar_hsa_circ_58350,RMVar_hsa_circ_19036,RMVar_hsa_circ_65582,RMVar_hsa_circ_13059,RMVar_hsa_circ_58461,RMVar_hsa_circ_5456,RMVar_hsa_circ_109009,RMVar_hsa_circ_142586,RMVar_hsa_circ_327839,RMVar_hsa_circ_61898,RMVar_hsa_circ_65965,RMVar_hsa_circ_374784,RMVar_hsa_circ_75084,RMVar_hsa_circ_25936,RMVar_hsa_circ_71054,RMVar_hsa_circ_36195,RMVar_hsa_circ_142590,RMVar_hsa_circ_39526,RMVar_hsa_circ_29174,RMVar_hsa_circ_351722,RMVar_hsa_circ_361899,RMVar_hsa_circ_280539,RMVar_hsa_circ_142595 36347 RMVar_ID_36347 Human_SNP_ID_424706199 A-to-I Human chr10 + 21672445 21672445 21672445 AGACGGGTTCAGCCTCCTGAGTAGCTGGGATTAGAGGCACACGTCACCACCCCCGGCTAATTTTT AGACGGGTTCAGCCTCCTGAGTAGCTGGGATTGGAGGCACACGTCACCACCCCCGGCTAATTTTT A G MLLT10 Ensembl:ENSG00000078403 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1371999679 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119150,RMVar_hsa_circ_142578,RMVar_hsa_circ_97333,RMVar_hsa_circ_60387,RMVar_hsa_circ_142579,RMVar_hsa_circ_58350,RMVar_hsa_circ_19036,RMVar_hsa_circ_65582,RMVar_hsa_circ_13059,RMVar_hsa_circ_58461,RMVar_hsa_circ_5456,RMVar_hsa_circ_109009,RMVar_hsa_circ_142586,RMVar_hsa_circ_327839,RMVar_hsa_circ_61898,RMVar_hsa_circ_65965,RMVar_hsa_circ_374784,RMVar_hsa_circ_75084,RMVar_hsa_circ_25936,RMVar_hsa_circ_71054,RMVar_hsa_circ_36195,RMVar_hsa_circ_142590,RMVar_hsa_circ_39526,RMVar_hsa_circ_29174,RMVar_hsa_circ_351722,RMVar_hsa_circ_361899,RMVar_hsa_circ_280539,RMVar_hsa_circ_142595 36348 RMVar_ID_36348 Human_SNP_ID_424707336 A-to-I Human chr10 + 21676296 21676296 21676296 AAAAGTAGCCCGGCATGGTGGCGGGTGCCTGTAGTCCTAGCTACTCGGAGAGGCTGAGGCAGGAG AAAAGTAGCCCGGCATGGTGGCGGGTGCCTGTGGTCCTAGCTACTCGGAGAGGCTGAGGCAGGAG A G MLLT10 Ensembl:ENSG00000078403 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1202797914 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_109009,RMVar_hsa_circ_142586,RMVar_hsa_circ_327839,RMVar_hsa_circ_61898,RMVar_hsa_circ_65965,RMVar_hsa_circ_374784,RMVar_hsa_circ_75084,RMVar_hsa_circ_25936,RMVar_hsa_circ_36195,RMVar_hsa_circ_142590,RMVar_hsa_circ_39526,RMVar_hsa_circ_29174,RMVar_hsa_circ_351722,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_80541,RMVar_hsa_circ_142598,RMVar_hsa_circ_142599,RMVar_hsa_circ_142596 36349 RMVar_ID_36349 Human_SNP_ID_424707850 A-to-I Human chr10 + 21678174 21678174 21678174 TTGACCAGGCTAGAGTGTAGTGGCCTGATCTCAGCTCACTGCCACCTCTGCCTCCCGAGTTAAAG TTGACCAGGCTAGAGTGTAGTGGCCTGATCTCGGCTCACTGCCACCTCTGCCTCCCGAGTTAAAG A G MLLT10 Ensembl:ENSG00000078403 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1442671867 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_109009,RMVar_hsa_circ_142586,RMVar_hsa_circ_327839,RMVar_hsa_circ_61898,RMVar_hsa_circ_65965,RMVar_hsa_circ_374784,RMVar_hsa_circ_75084,RMVar_hsa_circ_25936,RMVar_hsa_circ_36195,RMVar_hsa_circ_142590,RMVar_hsa_circ_39526,RMVar_hsa_circ_29174,RMVar_hsa_circ_351722,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_80541,RMVar_hsa_circ_142598,RMVar_hsa_circ_142599,RMVar_hsa_circ_142596 36350 RMVar_ID_36350 Human_SNP_ID_424708340 A-to-I Human chr10 + 21680331 21680331 21680331 TTGTTCAAGCGATTCTTGTGCCTCAGCCTCCCAAGTAGCTCGGATTACAGGCACGTGCCACCATG TTGTTCAAGCGATTCTTGTGCCTCAGCCTCCCGAGTAGCTCGGATTACAGGCACGTGCCACCATG A G MLLT10 Ensembl:ENSG00000078403 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1043781056 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_109009,RMVar_hsa_circ_142586,RMVar_hsa_circ_327839,RMVar_hsa_circ_61898,RMVar_hsa_circ_65965,RMVar_hsa_circ_374784,RMVar_hsa_circ_75084,RMVar_hsa_circ_25936,RMVar_hsa_circ_36195,RMVar_hsa_circ_142590,RMVar_hsa_circ_39526,RMVar_hsa_circ_29174,RMVar_hsa_circ_351722,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_80541,RMVar_hsa_circ_142598,RMVar_hsa_circ_142599,RMVar_hsa_circ_142596 36351 RMVar_ID_36351 Human_SNP_ID_424708446 A-to-I Human chr10 + 21680788 21680788 21680788 GAGGTCAGGAGTTCCAGACCAACCTGGCCAACATGGTGAAACCCTGTCTCTACTAAAGATACAAA GAGGTCAGGAGTTCCAGACCAACCTGGCCAACGTGGTGAAACCCTGTCTCTACTAAAGATACAAA A G MLLT10 Ensembl:ENSG00000078403 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs972746766 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_109009,RMVar_hsa_circ_142586,RMVar_hsa_circ_327839,RMVar_hsa_circ_61898,RMVar_hsa_circ_65965,RMVar_hsa_circ_374784,RMVar_hsa_circ_75084,RMVar_hsa_circ_25936,RMVar_hsa_circ_36195,RMVar_hsa_circ_142590,RMVar_hsa_circ_39526,RMVar_hsa_circ_29174,RMVar_hsa_circ_351722,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_80541,RMVar_hsa_circ_142598,RMVar_hsa_circ_142599,RMVar_hsa_circ_142596 36352 RMVar_ID_36352 Human_SNP_ID_424709912 A-to-I Human chr10 + 21686727 21686727 21686727 CCTTGGGGCCGTGCATGGTGGCTCATGCCTGCAATCCCAGCACTTTGGGAGGCCGAGGTGGCAGA CCTTGGGGCCGTGCATGGTGGCTCATGCCTGCGATCCCAGCACTTTGGGAGGCCGAGGTGGCAGA A G MLLT10 Ensembl:ENSG00000078403 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1213362814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11332722 RMVar_hsa_circ_1953,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_28893,RMVar_hsa_circ_142601,RMVar_hsa_circ_142602,RMVar_hsa_circ_332502,RMVar_hsa_circ_309660,RMVar_hsa_circ_142603 36353 RMVar_ID_36353 Human_SNP_ID_424716061 A-to-I Human chr10 + 21709841 21709841 21709841 CTCGGCTCAATCTCAACCTCCCAGGCTCAAGCAGTTCTCCCACCTCAGCCTCCCAAGTAGCTGGG CTCGGCTCAATCTCAACCTCCCAGGCTCAAGCGGTTCTCCCACCTCAGCCTCCCAAGTAGCTGGG A G MLLT10 Ensembl:ENSG00000078403 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350935916 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 36354 RMVar_ID_36354 Human_SNP_ID_424718629 A-to-I Human chr10 + 21718119 21718119 21718119 TGCCCACCTTGGCCTCCCAAAGTGCTGGGATTACAGGTGTGGGCCACTGCGCCCGGCCTCTATTT TGCCCACCTTGGCCTCCCAAAGTGCTGGGATTCCAGGTGTGGGCCACTGCGCCCGGCCTCTATTT A C MLLT10 Ensembl:ENSG00000078403 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs561498953 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97333,RMVar_hsa_circ_142579,RMVar_hsa_circ_58350,RMVar_hsa_circ_13059,RMVar_hsa_circ_58461,RMVar_hsa_circ_327839,RMVar_hsa_circ_65965,RMVar_hsa_circ_25936,RMVar_hsa_circ_36195,RMVar_hsa_circ_361899,RMVar_hsa_circ_268026,RMVar_hsa_circ_377400,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_53576,RMVar_hsa_circ_17582,RMVar_hsa_circ_28893,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_63935,RMVar_hsa_circ_271805,RMVar_hsa_circ_7458,RMVar_hsa_circ_270275,RMVar_hsa_circ_31712,RMVar_hsa_circ_142606,RMVar_hsa_circ_7510,RMVar_hsa_circ_13906,RMVar_hsa_circ_142608,RMVar_hsa_circ_6709,RMVar_hsa_circ_142607,RMVar_hsa_circ_142605 36355 RMVar_ID_36355 Human_SNP_ID_424720291 A-to-I Human chr10 + 21725603 21725603 21725603 TTTAGCTGGGCGTGGTGGCGGGCGCCTCCTGTAATCCCAGCCACTGGGAAGTCTGAGGCAGAATT TTTAGCTGGGCGTGGTGGCGGGCGCCTCCTGTTATCCCAGCCACTGGGAAGTCTGAGGCAGAATT A T MLLT10 Ensembl:ENSG00000078403 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417881501 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97333,RMVar_hsa_circ_142579,RMVar_hsa_circ_58350,RMVar_hsa_circ_13059,RMVar_hsa_circ_58461,RMVar_hsa_circ_327839,RMVar_hsa_circ_65965,RMVar_hsa_circ_25936,RMVar_hsa_circ_36195,RMVar_hsa_circ_361899,RMVar_hsa_circ_268026,RMVar_hsa_circ_377400,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_53576,RMVar_hsa_circ_17582,RMVar_hsa_circ_28893,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_63935,RMVar_hsa_circ_271805,RMVar_hsa_circ_7458,RMVar_hsa_circ_270275,RMVar_hsa_circ_31712,RMVar_hsa_circ_142606,RMVar_hsa_circ_7510,RMVar_hsa_circ_13906,RMVar_hsa_circ_142608,RMVar_hsa_circ_6709,RMVar_hsa_circ_142607,RMVar_hsa_circ_142605 36356 RMVar_ID_36356 Human_SNP_ID_424723754 A-to-I Human chr10 + 21738106 21738106 21738106 CCTGACCAACGTGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCCGGGTGTGGTGGCGC CCTGACCAACGTGGTGAAACCCCGTCTCTACTGAAAATACAAAAATTAGCCGGGTGTGGTGGCGC A G MLLT10 Ensembl:ENSG00000078403 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs542590018 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63935 36357 RMVar_ID_36357 Human_SNP_ID_424754422 A-to-I Human chr10 - 21845415 21845415 21845415 TGGAGGCGGAGGTTGCAGTGAGCCGAGATCACACCACTGTGCTCCAGCCTGGGCAACAGAACAAG TGGAGGCGGAGGTTGCAGTGAGCCGAGATCACGCCACTGTGCTCCAGCCTGGGCAACAGAACAAG T C DNAJC1 Ensembl:ENSG00000136770 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017000258 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24800273 RMVar_hsa_circ_89546,RMVar_hsa_circ_105257,RMVar_hsa_circ_142614,RMVar_hsa_circ_142615,RMVar_hsa_circ_112144,RMVar_hsa_circ_142617,RMVar_hsa_circ_112305,RMVar_hsa_circ_346178,RMVar_hsa_circ_142616,RMVar_hsa_circ_286035,RMVar_hsa_circ_85371,RMVar_hsa_circ_19044,RMVar_hsa_circ_142618 36358 RMVar_ID_36358 Human_SNP_ID_424759356 A-to-I Human chr10 - 21864379 21864379 21864379 CTGACCTCGTGATCCACCTGCCTTGGCCTCCCAGGGTGCTGGGATTACAGGCATGAGCCACTGCA CTGACCTCGTGATCCACCTGCCTTGGCCTCCCCGGGTGCTGGGATTACAGGCATGAGCCACTGCA T G DNAJC1 Ensembl:ENSG00000136770 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs546529737 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89546,RMVar_hsa_circ_105257,RMVar_hsa_circ_142614,RMVar_hsa_circ_142615,RMVar_hsa_circ_112144,RMVar_hsa_circ_142617,RMVar_hsa_circ_112305,RMVar_hsa_circ_346178,RMVar_hsa_circ_142616,RMVar_hsa_circ_286035,RMVar_hsa_circ_85371,RMVar_hsa_circ_19044,RMVar_hsa_circ_142618 36359 RMVar_ID_36359 Human_SNP_ID_424762208 A-to-I Human chr10 - 21875862 21875862 21875862 GAAGTGCAACAGCATGATCTCACCTCGCTGCAACCTCCGCCTCCCAGGTTCAAGTGATTCTCCTG GAAGTGCAACAGCATGATCTCACCTCGCTGCACCCTCCGCCTCCCAGGTTCAAGTGATTCTCCTG T G DNAJC1 Ensembl:ENSG00000136770 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1364857452 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89546,RMVar_hsa_circ_105257,RMVar_hsa_circ_142614,RMVar_hsa_circ_142615,RMVar_hsa_circ_112144,RMVar_hsa_circ_142617,RMVar_hsa_circ_112305,RMVar_hsa_circ_346178,RMVar_hsa_circ_142616,RMVar_hsa_circ_286035,RMVar_hsa_circ_85371,RMVar_hsa_circ_19044,RMVar_hsa_circ_142618 36360 RMVar_ID_36360 Human_SNP_ID_424781873 A-to-I Human chr10 - 21956301 21956301 21956301 CAGTGTTGAGGTGAGACTTTTAAAAGGTGATTAGGTCATGAAGGCTCTACCCTCATGAAAGTGTT CAGTGTTGAGGTGAGACTTTTAAAAGGTGATTCGGTCATGAAGGCTCTACCCTCATGAAAGTGTT T G DNAJC1 Ensembl:ENSG00000136770 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1380788587 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89546,RMVar_hsa_circ_142614 36361 RMVar_ID_36361 Human_SNP_ID_424789388 A-to-I Human chr10 - 21986908 21986908 21986908 CAAAAAATTGTTGGGTGTGGTGGCAGCTGTCTATAAGCCCAACTACTCGGGAGGCTGAGGCAGGA CAAAAAATTGTTGGGTGTGGTGGCAGCTGTCTGTAAGCCCAACTACTCGGGAGGCTGAGGCAGGA T C DNAJC1 Ensembl:ENSG00000136770 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1446282785 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89546,RMVar_hsa_circ_142614 36362 RMVar_ID_36362 Human_SNP_ID_424933441 A-to-I Human chr10 - 22562424 22562424 22562424 CTGCCTCAGCCTCCCTAGTAGCTGGGACTACAAGCGCCTGTCACTACGCTTGGCTAATTTTTTTG CTGCCTCAGCCTCCCTAGTAGCTGGGACTACAGGCGCCTGTCACTACGCTTGGCTAATTTTTTTG T C PIP4K2A Ensembl:ENSG00000150867 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1425270985 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_142633,RMVar_hsa_circ_76969,RMVar_hsa_circ_318438,RMVar_hsa_circ_112978,RMVar_hsa_circ_3590,RMVar_hsa_circ_142635,RMVar_hsa_circ_29641,RMVar_hsa_circ_82944,RMVar_hsa_circ_355251,RMVar_hsa_circ_142636,RMVar_hsa_circ_356562,RMVar_hsa_circ_314152,RMVar_hsa_circ_142637 36363 RMVar_ID_36363 Human_SNP_ID_424943163 A-to-I Human chr10 - 22598166 22598166 22598166 CTATGTAGACACAGAGCCTTACTATGCTGCCCAGGCTGGTCCCAAACTCCTGGCCTCAAGTGATC CTATGTAGACACAGAGCCTTACTATGCTGCCCGGGCTGGTCCCAAACTCCTGGCCTCAAGTGATC T C PIP4K2A Ensembl:ENSG00000150867 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1403741472 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11334890 RMVar_hsa_circ_3590,RMVar_hsa_circ_29641,RMVar_hsa_circ_355251,RMVar_hsa_circ_142638,RMVar_hsa_circ_312981,RMVar_hsa_circ_364370,RMVar_hsa_circ_60069,RMVar_hsa_circ_60361,RMVar_hsa_circ_142641,RMVar_hsa_circ_305294,RMVar_hsa_circ_142644 36364 RMVar_ID_36364 Human_SNP_ID_424959287 A-to-I Human chr10 - 22659549 22659549 22659549 GCATTAATGTCTCAATGACCCCAGACCTTGCTACCGTCCTCCTCTCAACTCCTGTGGCACATTTA GCATTAATGTCTCAATGACCCCAGACCTTGCTGCCGTCCTCCTCTCAACTCCTGTGGCACATTTA T C PIP4K2A Ensembl:ENSG00000150867 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031971330 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5435335 36365 RMVar_ID_36365 Human_SNP_ID_425074487 A-to-I Human chr10 + 23123175 23123175 23123175 ATCTCGGCTCACTGCAACTTCTGCCACCCCCGAGTTCAAAAGATTCTCCTGCCTCAGCCTCCTGA ATCTCGGCTCACTGCAACTTCTGCCACCCCCGCGTTCAAAAGATTCTCCTGCCTCAGCCTCCTGA A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569318223 Functional Loss SNV dbSNP153 33..33 33 - - - 36366 RMVar_ID_36366 Human_SNP_ID_425357203 A-to-I Human chr10 + 24230529 24230529 24230529 GTTTTGTTTTTTTTTTTTTTTTTTTTTGAGACAGAGTCTCACTCTTTCATCCAGGCTGGAATGCA GTTTTGTTTTTTTTTTTTTTTTTTTTTGAGACGGAGTCTCACTCTTTCATCCAGGCTGGAATGCA A G KIAA1217 Ensembl:ENSG00000120549 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1435046254 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25657 36367 RMVar_ID_36367 Human_SNP_ID_425363968 A-to-I Human chr10 + 24258792 24258792 24258792 TTTTTTGTATTTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGGTCTCGATCTCCTGA TTTTTTGTATTTTTTAGTAGAGACGGGGTTTCTCCGTGTTAGCCAGGATGGTCTCGATCTCCTGA A T KIAA1217 Ensembl:ENSG00000120549 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1403598212 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25657 36368 RMVar_ID_36368 Human_SNP_ID_425372026 A-to-I Human chr10 + 24291432 24291432 24291432 GGTGCCTGAAATCCCAGCTATTAGGGTGGCTGAAGCAAGAGAATCACTTGAACCTGGGAGGCGGA GGTGCCTGAAATCCCAGCTATTAGGGTGGCTGCAGCAAGAGAATCACTTGAACCTGGGAGGCGGA A C KIAA1217 Ensembl:ENSG00000120549 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1447514712 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25657 36369 RMVar_ID_36369 Human_SNP_ID_425372027 A-to-I Human chr10 + 24291436 24291436 24291436 CCTGAAATCCCAGCTATTAGGGTGGCTGAAGCAAGAGAATCACTTGAACCTGGGAGGCGGAGGTT CCTGAAATCCCAGCTATTAGGGTGGCTGAAGCGAGAGAATCACTTGAACCTGGGAGGCGGAGGTT A G KIAA1217 Ensembl:ENSG00000120549 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs956426059 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25657 36370 RMVar_ID_36370 Human_SNP_ID_425431941 A-to-I Human chr10 + 24530993 24530993 24530993 GAGGCAGACAGATTGCTTGATCCCAGGAGTTCAAGACCAGCCTGTGCAACATGGCAGAAACCCCG GAGGCAGACAGATTGCTTGATCCCAGGAGTTCGAGACCAGCCTGTGCAACATGGCAGAAACCCCG A G KIAA1217 Ensembl:ENSG00000120549 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs994915573 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_352473,RMVar_hsa_circ_32578,RMVar_hsa_circ_53836,RMVar_hsa_circ_362504,RMVar_hsa_circ_359655,RMVar_hsa_circ_323805,RMVar_hsa_circ_70646,RMVar_hsa_circ_322398 36371 RMVar_ID_36371 Human_SNP_ID_425467643 A-to-I Human chr10 - 24663689 24663689 24663689 CCTCTTCTCTACTAAAAATAAAAAAATTAGCCAGGGGTGGGGATGCACGCTTCTAATCCCAGCTA CCTCTTCTCTACTAAAAATAAAAAAATTAGCCGGGGGTGGGGATGCACGCTTCTAATCCCAGCTA T C ARHGAP21 Ensembl:ENSG00000107863 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs771606065 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2959,RMVar_hsa_circ_142682,RMVar_hsa_circ_347323,RMVar_hsa_circ_290657,RMVar_hsa_circ_142680,RMVar_hsa_circ_272921,RMVar_hsa_circ_363963,RMVar_hsa_circ_142683,RMVar_hsa_circ_44917 36372 RMVar_ID_36372 Human_SNP_ID_425479105 A-to-I Human chr10 - 24710911 24710911 24710911 TTTCGTATTTTTAATAGAGATGGGGTTTCGCCATGTTGGCCATGCTGTTCTCGAACTCCTGACCT TTTCGTATTTTTAATAGAGATGGGGTTTCGCCGTGTTGGCCATGCTGTTCTCGAACTCCTGACCT T C ARHGAP21 Ensembl:ENSG00000107863 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs933401646 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2959,RMVar_hsa_circ_347323,RMVar_hsa_circ_363963,RMVar_hsa_circ_142683 36373 RMVar_ID_36373 Human_SNP_ID_425522726 A-to-I Human chr10 - 24881950 24881950 24881950 CGCCTGACTCAGCCTCCCAAAGTTCTGGGATTACAGATATGAGCCACCGTGCCCCGCAAACTGAG CGCCTGACTCAGCCTCCCAAAGTTCTGGGATTGCAGATATGAGCCACCGTGCCCCGCAAACTGAG T C PRTFDC1 Ensembl:ENSG00000099256 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1162798810 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_345733,RMVar_hsa_circ_142690,RMVar_hsa_circ_142693,RMVar_hsa_circ_106590,RMVar_hsa_circ_142694,RMVar_hsa_circ_313156 36374 RMVar_ID_36374 Human_SNP_ID_425652292 A-to-I Human chr10 + 25397129 25397129 25397129 CTATCACTTCAGCATATAACATAGCCCAACCAAAAGAGAGAATGTCCCATCATATTTACGGATCC CTATCACTTCAGCATATAACATAGCCCAACCAGAAGAGAGAATGTCCCATCATATTTACGGATCC A G GPR158 Ensembl:ENSG00000151025 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1046470315 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25273,RMVar_hsa_circ_52956,RMVar_hsa_circ_277162,RMVar_hsa_circ_142702,RMVar_hsa_circ_142703 36375 RMVar_ID_36375 Human_SNP_ID_425652495 A-to-I Human chr10 + 25398055 25398055 25398055 TAGCCCATGAGAAAACAGGGACTTCGACTACTACAATTGCAGGGAAGTAAATTCTTCCAACAGCC TAGCCCATGAGAAAACAGGGACTTCGACTACTGCAATTGCAGGGAAGTAAATTCTTCCAACAGCC A G GPR158 Ensembl:ENSG00000151025 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1031533900 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25273,RMVar_hsa_circ_52956,RMVar_hsa_circ_277162,RMVar_hsa_circ_142702,RMVar_hsa_circ_142703 36376 RMVar_ID_36376 Human_SNP_ID_425922967 A-to-I Human chr10 + 26497048 26497048 26497048 CATCTCTACAAAAAGTAAAAAATAAAAAAATTAGCCAAGCGTGGTGGCATGTGCCTGTGGTCTCA CATCTCTACAAAAAGTAAAAAATAAAAAAATTTGCCAAGCGTGGTGGCATGTGCCTGTGGTCTCA A T APBB1IP Ensembl:ENSG00000077420 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1052659700 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_65233,RMVar_hsa_circ_345608,RMVar_hsa_circ_365727,RMVar_hsa_circ_357793,RMVar_hsa_circ_357604,RMVar_hsa_circ_59649 36377 RMVar_ID_36377 Human_SNP_ID_425924919 A-to-I Human chr10 + 26504984 26504984 26504984 CCCTATGTTGCCTAGGCTTTTCTCGGACTCCTAGGCTCAAGCGCGCCACCCATCTCAGCCTCACA CCCTATGTTGCCTAGGCTTTTCTCGGACTCCTCGGCTCAAGCGCGCCACCCATCTCAGCCTCACA A C APBB1IP Ensembl:ENSG00000077420 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1467002311 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_326880,RMVar_hsa_circ_65233,RMVar_hsa_circ_365727,RMVar_hsa_circ_357604,RMVar_hsa_circ_360245,RMVar_hsa_circ_334151,RMVar_hsa_circ_353476,RMVar_hsa_circ_142721,RMVar_hsa_circ_354805,RMVar_hsa_circ_351080 36378 RMVar_ID_36378 Human_SNP_ID_425927423 A-to-I Human chr10 + 26515066 26515066 26515066 GCTAATTTTTTTTTTTTTTTTTGTATTTTAGTAGAGATGGGGTTTCACCGTGTTGGCCAGGGTGA GCTAATTTTTTTTTTTTTTTTTGTATTTTAGTTGAGATGGGGTTTCACCGTGTTGGCCAGGGTGA A T APBB1IP Ensembl:ENSG00000077420 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1427901590 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55494,RMVar_hsa_circ_357604,RMVar_hsa_circ_360245,RMVar_hsa_circ_354805,RMVar_hsa_circ_358827,RMVar_hsa_circ_105427,RMVar_hsa_circ_142723,RMVar_hsa_circ_68662 36379 RMVar_ID_36379 Human_SNP_ID_425978356 A-to-I Human chr10 + 26699018 26699018 26699018 GGGGTGGTGCATGCCTGTAGTTCTACCTACTCAGGAGCCTGAGGGAGGAGGATTGTTCGATCCCA GGGGTGGTGCATGCCTGTAGTTCTACCTACTCCGGAGCCTGAGGGAGGAGGATTGTTCGATCCCA A C PDSS1 Ensembl:ENSG00000148459 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1364237650 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18592066 RMVar_hsa_circ_112312,RMVar_hsa_circ_142726 36380 RMVar_ID_36380 Human_SNP_ID_425983131 A-to-I Human chr10 + 26718614 26718614 26718614 GAAACCCCATCTCTACTAAAAATACAAACATTAGCTGGATGTGGTGGTGTGCACATGTAATCCAA GAAACCCCATCTCTACTAAAAATACAAACATTCGCTGGATGTGGTGGTGTGCACATGTAATCCAA A C AL390961.2,PDSS1 Ensembl:ENSG00000235843,Ensembl:ENSG00000148459 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1419911269 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_142728,RMVar_hsa_circ_315691,RMVar_hsa_circ_338630,RMVar_hsa_circ_287003,RMVar_hsa_circ_142730,RMVar_hsa_circ_142729,RMVar_hsa_circ_142734,RMVar_hsa_circ_142738,RMVar_hsa_circ_111456,RMVar_hsa_circ_285245,RMVar_hsa_circ_295943,RMVar_hsa_circ_308902,RMVar_hsa_circ_290541,RMVar_hsa_circ_142739,RMVar_hsa_circ_142736,RMVar_hsa_circ_142737,RMVar_hsa_circ_142735,RMVar_hsa_circ_142740,RMVar_hsa_circ_23756,RMVar_hsa_circ_314162,RMVar_hsa_circ_370144,RMVar_hsa_circ_313299,RMVar_hsa_circ_142741 36381 RMVar_ID_36381 Human_SNP_ID_425984678 A-to-I Human chr10 + 26724798 26724797 26724799 TGGGGGTTTGCCATGTTGGCCGGGCTGGTCTCAAACTCCTGCCCTCAAGTGATCCACCCACCTTG TGGGGGTTTGCCATGTTGGCCGGGCTGGTCTC__ACTCCTGCCCTCAAGTGATCCACCCACCTTG CAA C PDSS1 Ensembl:ENSG00000148459 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1197770509 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_11337862,Human_RBP_ID_24802101 RMVar_hsa_circ_13693,RMVar_hsa_circ_142728,RMVar_hsa_circ_338630,RMVar_hsa_circ_142738,RMVar_hsa_circ_111456,RMVar_hsa_circ_285245,RMVar_hsa_circ_142739,RMVar_hsa_circ_142737,RMVar_hsa_circ_23756,RMVar_hsa_circ_61166,RMVar_hsa_circ_361614 36382 RMVar_ID_36382 Human_SNP_ID_425985436 A-to-I Human chr10 + 26728029 26728029 26728029 TACCAGGAGGCGCGTGCTGTCTTGTCTGTCCCATTACTGGTGATGCATGCCTGGATCGCTTGATT TACCAGGAGGCGCGTGCTGTCTTGTCTGTCCCGTTACTGGTGATGCATGCCTGGATCGCTTGATT A G PDSS1 Ensembl:ENSG00000148459 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs3118153 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_4045,GWAS_ID_4046,GWAS_ID_4047,GWAS_ID_4048,GWAS_ID_4049,GWAS_ID_4050,GWAS_ID_4051 RMVar_hsa_circ_13693,RMVar_hsa_circ_142728,RMVar_hsa_circ_338630,RMVar_hsa_circ_142738,RMVar_hsa_circ_111456,RMVar_hsa_circ_285245,RMVar_hsa_circ_142739,RMVar_hsa_circ_142737,RMVar_hsa_circ_23756,RMVar_hsa_circ_61166,RMVar_hsa_circ_361614 36383 RMVar_ID_36383 Human_SNP_ID_425985437 A-to-I Human chr10 + 26728029 26728029 26728029 TACCAGGAGGCGCGTGCTGTCTTGTCTGTCCCATTACTGGTGATGCATGCCTGGATCGCTTGATT TACCAGGAGGCGCGTGCTGTCTTGTCTGTCCCTTTACTGGTGATGCATGCCTGGATCGCTTGATT A T PDSS1 Ensembl:ENSG00000148459 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs3118153 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_4045,GWAS_ID_4046,GWAS_ID_4047,GWAS_ID_4048,GWAS_ID_4049,GWAS_ID_4050,GWAS_ID_4051 RMVar_hsa_circ_13693,RMVar_hsa_circ_142728,RMVar_hsa_circ_338630,RMVar_hsa_circ_142738,RMVar_hsa_circ_111456,RMVar_hsa_circ_285245,RMVar_hsa_circ_142739,RMVar_hsa_circ_142737,RMVar_hsa_circ_23756,RMVar_hsa_circ_61166,RMVar_hsa_circ_361614 36384 RMVar_ID_36384 Human_SNP_ID_425985525 A-to-I Human chr10 + 26728367 26728367 26728367 CAAAAATTAGCCGGGCGTAGTGGCAGGCGCCTATAATCCCAGCTACTCTGGAGGCTGATACAGGA CAAAAATTAGCCGGGCGTAGTGGCAGGCGCCTGTAATCCCAGCTACTCTGGAGGCTGATACAGGA A G PDSS1 Ensembl:ENSG00000148459 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1430086864 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13693,RMVar_hsa_circ_142728,RMVar_hsa_circ_338630,RMVar_hsa_circ_142738,RMVar_hsa_circ_111456,RMVar_hsa_circ_285245,RMVar_hsa_circ_142739,RMVar_hsa_circ_142737,RMVar_hsa_circ_23756,RMVar_hsa_circ_61166,RMVar_hsa_circ_361614 36385 RMVar_ID_36385 Human_SNP_ID_425986131 A-to-I Human chr10 + 26730444 26730443 26730445 CCAGCCTGGGCAACATGGCGAAACCTCTGTCTACAAGGAATACAAAAATTAGCTGGGTGTGGTAG CCAGCCTGGGCAACATGGCGAAACCTCTGTCT__AAGGAATACAAAAATTAGCTGGGTGTGGTAG TAC T PDSS1 Ensembl:ENSG00000148459 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1260784642 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_13693,RMVar_hsa_circ_142728,RMVar_hsa_circ_338630,RMVar_hsa_circ_142738,RMVar_hsa_circ_111456,RMVar_hsa_circ_285245,RMVar_hsa_circ_142739,RMVar_hsa_circ_23756,RMVar_hsa_circ_61166,RMVar_hsa_circ_361614 36386 RMVar_ID_36386 Human_SNP_ID_425988725 A-to-I Human chr10 + 26741223 26741223 26741223 TATACCTCCCCAGGCCAGGCGCGGTGGCTCACACCTGTAATCCCAGCACTTGGGGAGGCTGAGGT TATACCTCCCCAGGCCAGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTGGGGAGGCTGAGGT A G PDSS1 Ensembl:ENSG00000148459 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs577039088 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13693,RMVar_hsa_circ_142728,RMVar_hsa_circ_338630,RMVar_hsa_circ_111456,RMVar_hsa_circ_142739,RMVar_hsa_circ_377228 36387 RMVar_ID_36387 Human_SNP_ID_425989000 A-to-I Human chr10 + 26742151 26742151 26742151 CGCCCACCTCGGCCTCCCAGAGTGCTGGGATTACAGGCGTGTGCCACCACGCCTGGCCAGAACCA CGCCCACCTCGGCCTCCCAGAGTGCTGGGATTGCAGGCGTGTGCCACCACGCCTGGCCAGAACCA A G PDSS1 Ensembl:ENSG00000148459 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1447431771 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13693,RMVar_hsa_circ_142728,RMVar_hsa_circ_338630,RMVar_hsa_circ_111456,RMVar_hsa_circ_142739,RMVar_hsa_circ_377228 36388 RMVar_ID_36388 Human_SNP_ID_425993285 A-to-I Human chr10 - 26760724 26760724 26760724 CTCCATGCCCAGCTAATTGTTGTATTTTTAGTAGACACGGGTTTTCGCCATGATGGCCAGGCTGG CTCCATGCCCAGCTAATTGTTGTATTTTTAGTGGACACGGGTTTTCGCCATGATGGCCAGGCTGG T C ABI1 Ensembl:ENSG00000136754 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1406826373 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_142744,RMVar_hsa_circ_60583,RMVar_hsa_circ_360757,RMVar_hsa_circ_279599 36389 RMVar_ID_36389 Human_SNP_ID_425993440 A-to-I Human chr10 - 26761210 26761210 26761210 TGGTTGGCTGGGAGTGGTGACTCACACCTGTAATCCAGCATTTTGGGAGGCCAAGGTGGGAGGAT TGGTTGGCTGGGAGTGGTGACTCACACCTGTAGTCCAGCATTTTGGGAGGCCAAGGTGGGAGGAT T C ABI1 Ensembl:ENSG00000136754 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs973607402 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_142744,RMVar_hsa_circ_60583,RMVar_hsa_circ_360757,RMVar_hsa_circ_279599 36390 RMVar_ID_36390 Human_SNP_ID_426010820 A-to-I Human chr10 - 26835409 26835409 26835409 CACCACACCCTGCTAATTTTTAAATTTTTTGTAGAGACGAGGTCTTGCTGTGCTGCTCAGGCTGG CACCACACCCTGCTAATTTTTAAATTTTTTGTGGAGACGAGGTCTTGCTGTGCTGCTCAGGCTGG T C ABI1 Ensembl:ENSG00000136754 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1401967189 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121568,RMVar_hsa_circ_142747 36391 RMVar_ID_36391 Human_SNP_ID_426015152 A-to-I Human chr10 - 26852474 26852474 26852474 CAGATGCTTATTTTATTTTATTTTTTTGAGACAGAGTTTCGTTCTTGTTGCCCAGGCTAGAGTAT CAGATGCTTATTTTATTTTATTTTTTTGAGACGGAGTTTCGTTCTTGTTGCCCAGGCTAGAGTAT T C ABI1 Ensembl:ENSG00000136754 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1159137467 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121568,RMVar_hsa_circ_142747 36392 RMVar_ID_36392 Human_SNP_ID_426046052 A-to-I Human chr10 - 26970103 26970103 26970103 CTAACAGAAACTAGGGCCGGGCGAAGTGGCTCACACCTGTAATCCCAGCACTTTGGGCGGCTGAG CTAACAGAAACTAGGGCCGGGCGAAGTGGCTCGCACCTGTAATCCCAGCACTTTGGGCGGCTGAG T C lnc-ANKRD26-1 RNACentral:URS00008B437F lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1266913065 Functional Loss SNV dbSNP153 33..33 33 - - - 36393 RMVar_ID_36393 Human_SNP_ID_426046317 A-to-I Human chr10 - 26971192 26971192 26971192 TTTAGTAGAGACAGGGTTTGGCCATGATGGCCAGGTTGGTCTCAAACTCCTGAGCTCAAGTGATA TTTAGTAGAGACAGGGTTTGGCCATGATGGCCGGGTTGGTCTCAAACTCCTGAGCTCAAGTGATA T C lnc-ANKRD26-1 RNACentral:URS00008B437F lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs561011589 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24802562 36394 RMVar_ID_36394 Human_SNP_ID_426072751 A-to-I Human chr10 - 27080105 27080105 27080105 TTGCCCAGGCTGGAGTGCTACAGCATGATCTCAGCTCACTGCAATCTCTGCTTCCTGGGTTCACA TTGCCCAGGCTGGAGTGCTACAGCATGATCTCGGCTCACTGCAATCTCTGCTTCCTGGGTTCACA T C ANKRD26 Ensembl:ENSG00000107890 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404677141 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1120483 RMVar_hsa_circ_86857,RMVar_hsa_circ_142760,RMVar_hsa_circ_142768,RMVar_hsa_circ_76652,RMVar_hsa_circ_142776,RMVar_hsa_circ_349940,RMVar_hsa_circ_350400,RMVar_hsa_circ_312394,RMVar_hsa_circ_348161,RMVar_hsa_circ_321584,RMVar_hsa_circ_299092,RMVar_hsa_circ_267213,RMVar_hsa_circ_142781,RMVar_hsa_circ_293741,RMVar_hsa_circ_312164,RMVar_hsa_circ_287130,RMVar_hsa_circ_142782,RMVar_hsa_circ_142780,RMVar_hsa_circ_73376,RMVar_hsa_circ_300967,RMVar_hsa_circ_368764,RMVar_hsa_circ_269464,RMVar_hsa_circ_142785 36395 RMVar_ID_36395 Human_SNP_ID_426078302 A-to-I Human chr10 + 27101294 27101294 27101294 AGACGCAAGCCACCACGCCCGGCTATTTTTGCATTTTTTGTAGAGACAGGGTCTCACCATGTTGC AGACGCAAGCCACCACGCCCGGCTATTTTTGCGTTTTTTGTAGAGACAGGGTCTCACCATGTTGC A G lnc-MASTL-5 RNACentral:URS0000D5784D lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1016823764 Functional Loss SNV dbSNP153 33..33 33 - - - 36396 RMVar_ID_36396 Human_SNP_ID_426081027 A-to-I Human chr10 - 27111467 27111467 27111467 CCTTTTGGCATGGTGCCATGGCTCACATCTGTAATCCCAGCACTTTTGGAGGCTGAGGCGGGTGG CCTTTTGGCATGGTGCCATGGCTCACATCTGTCATCCCAGCACTTTTGGAGGCTGAGGCGGGTGG T G YME1L1 Ensembl:ENSG00000136758 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1294910823 Functional Loss SNV dbSNP153 33..33 33 - - - 36397 RMVar_ID_36397 Human_SNP_ID_426086166 A-to-I Human chr10 - 27132627 27132627 27132627 TTTTAGTAGAGACGGCGTTTCACCGTTAGCCAAGATGGTCTCGATCTCCTCACCTTGCGATCTGC TTTTAGTAGAGACGGCGTTTCACCGTTAGCCAGGATGGTCTCGATCTCCTCACCTTGCGATCTGC T C YME1L1 Ensembl:ENSG00000136758 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1431672273 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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,RMVar_hsa_circ_142811,RMVar_hsa_circ_279499,RMVar_hsa_circ_329634,RMVar_hsa_circ_142810 36398 RMVar_ID_36398 Human_SNP_ID_426088766 A-to-I Human chr10 - 27143125 27143112 27143125 CCTCAGGTTATCCACCCACCTCTGCCTCCCAAAGTGCTGGAATTACAGGCGTGAGCCACCACACC CCTCAGGTTATCCACCCACCTCTGCCTCCCAA_____________CAGGCGTGAGCCACCACACC GTAATTCCAGCACT G YME1L1 Ensembl:ENSG00000136758 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202930583 Functional Loss DEL dbSNP153 33..45 33 - - - RMVar_hsa_circ_20627,RMVar_hsa_circ_142789,RMVar_hsa_circ_18071,RMVar_hsa_circ_32462,RMVar_hsa_circ_142800,RMVar_hsa_circ_48914,RMVar_hsa_circ_313908,RMVar_hsa_circ_142806,RMVar_hsa_circ_142808,RMVar_hsa_circ_315022,RMVar_hsa_circ_142811,RMVar_hsa_circ_329634,RMVar_hsa_circ_354035,RMVar_hsa_circ_142815,RMVar_hsa_circ_142813,RMVar_hsa_circ_378103,RMVar_hsa_circ_53401,RMVar_hsa_circ_142817,RMVar_hsa_circ_273725,RMVar_hsa_circ_371793,RMVar_hsa_circ_142816 36399 RMVar_ID_36399 Human_SNP_ID_426090981 A-to-I Human chr10 - 27151054 27151054 27151054 GGGTGTGGTGGCCTGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTCGAA GGGTGTGGTGGCCTGCGCCTGTAGTCCCAGCTGCTCGGGAGGCTGAGGCAGGAGAATCACTCGAA T C YME1L1 Ensembl:ENSG00000136758 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs533961686 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86010,RMVar_hsa_circ_142819 36400 RMVar_ID_36400 Human_SNP_ID_426090984 A-to-I Human chr10 - 27151064 27151064 27151064 AAAAATAGCTGGGTGTGGTGGCCTGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAAATAGCTGGGTGTGGTGGCCTGCGCCTGTGGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA T C YME1L1 Ensembl:ENSG00000136758 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs547372841 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86010,RMVar_hsa_circ_142819 36401 RMVar_ID_36401 Human_SNP_ID_426093881 A-to-I Human chr10 + 27161317 27161317 27161317 ATCACCTGAGGTCAGGAGTTAGAGACCAGCCTAGCTAACGTGGCAAAACCCCATCTCTACTAAAA ATCACCTGAGGTCAGGAGTTAGAGACCAGCCTGGCTAACGTGGCAAAACCCCATCTCTACTAAAA A G MASTL Ensembl:ENSG00000120539 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1465609783 Functional Loss SNV dbSNP153 33..33 33 - - - 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_142828 36402 RMVar_ID_36402 Human_SNP_ID_426094121 A-to-I Human chr10 + 27162522 27162522 27162522 GAAACCCCATCTCTACTAAAAATACAAAAATTAGCTGAGTGTGGTGGCACACGCCTGTAGTCCCA GAAACCCCATCTCTACTAAAAATACAAAAATTTGCTGAGTGTGGTGGCACACGCCTGTAGTCCCA A T MASTL Ensembl:ENSG00000120539 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1411785297 Functional Loss SNV dbSNP153 33..33 33 - - - 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_142828 36403 RMVar_ID_36403 Human_SNP_ID_426094138 A-to-I Human chr10 + 27162610 27162610 27162610 AGAATTGCTTAAACCTGGGAGGCAGAGGTTGCAGTGAGCCAAGATCACGACACTGCACTCTAGCC AGAATTGCTTAAACCTGGGAGGCAGAGGTTGCGGTGAGCCAAGATCACGACACTGCACTCTAGCC A G MASTL Ensembl:ENSG00000120539 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1476476194 Functional Loss SNV dbSNP153 33..33 33 - - - 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_142828 36404 RMVar_ID_36404 Human_SNP_ID_426094226 A-to-I Human chr10 + 27162994 27162994 27162994 GCTGGAGTGCAATGGCGTGATCTCGGCTCACTACAACATCCACCTCCCGGGTTCAAGCAATTCTC GCTGGAGTGCAATGGCGTGATCTCGGCTCACTGCAACATCCACCTCCCGGGTTCAAGCAATTCTC A G MASTL Ensembl:ENSG00000120539 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1564485426 Functional Loss SNV dbSNP153 33..33 33 - - - 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_142828 36405 RMVar_ID_36405 Human_SNP_ID_426094239 A-to-I Human chr10 + 27163020 27163020 27163020 CTCACTACAACATCCACCTCCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTTCTGAGTAGCTGGG CTCACTACAACATCCACCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTTCTGAGTAGCTGGG A G MASTL Ensembl:ENSG00000120539 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs948576154 Functional Loss SNV dbSNP153 33..33 33 - - - 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_142828 36406 RMVar_ID_36406 Human_SNP_ID_426096957 A-to-I Human chr10 + 27173755 27173755 27173755 GGCATCCACCATCATGCCCGCCTAATTTTTGTATTTTTAGTAGAGACAGTTTCACCATGTTAGCC GGCATCCACCATCATGCCCGCCTAATTTTTGTGTTTTTAGTAGAGACAGTTTCACCATGTTAGCC A G MASTL Ensembl:ENSG00000120539 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1170981227 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_366834,RMVar_hsa_circ_326591,RMVar_hsa_circ_142821,RMVar_hsa_circ_142822,RMVar_hsa_circ_51633,RMVar_hsa_circ_323753,RMVar_hsa_circ_142832,RMVar_hsa_circ_280240,RMVar_hsa_circ_142835,RMVar_hsa_circ_279663,RMVar_hsa_circ_303255,RMVar_hsa_circ_142836,RMVar_hsa_circ_281255,RMVar_hsa_circ_142838 36407 RMVar_ID_36407 Human_SNP_ID_426097708 A-to-I Human chr10 + 27177019 27177019 27177019 GGCACCTGCCCCCATGCTCGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATCATGG GGCACCTGCCCCCATGCTCGGCTAATTTTTGTGTTTTTAGTAGAGACGGGGTTTCACCATCATGG A G MASTL Ensembl:ENSG00000120539 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs781088543 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_366834,RMVar_hsa_circ_326591,RMVar_hsa_circ_142821,RMVar_hsa_circ_142822,RMVar_hsa_circ_51633,RMVar_hsa_circ_323753,RMVar_hsa_circ_142832,RMVar_hsa_circ_280240,RMVar_hsa_circ_142835,RMVar_hsa_circ_279663,RMVar_hsa_circ_303255,RMVar_hsa_circ_142836,RMVar_hsa_circ_281255,RMVar_hsa_circ_142838 36408 RMVar_ID_36408 Human_SNP_ID_426098925 A-to-I Human chr10 + 27182162 27182162 27182162 AGTCCCAGCTACTCTGGAGGCTGAGGCAGGAGAATCGCTTCAACCCGGGAGGCGGACATTGCAGT AGTCCCAGCTACTCTGGAGGCTGAGGCAGGAGCATCGCTTCAACCCGGGAGGCGGACATTGCAGT A C MASTL Ensembl:ENSG00000120539 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1166019178 Functional Loss SNV dbSNP153 33..33 33 - - - 36409 RMVar_ID_36409 Human_SNP_ID_426099051 A-to-I Human chr10 + 27182649 27182649 27182649 ACCTGTAGTTCCAGCTACTTGGGGGCTTAGGCAGGAAGATTACTTGAGCCCAGGAGGTCGAGGCT ACCTGTAGTTCCAGCTACTTGGGGGCTTAGGCCGGAAGATTACTTGAGCCCAGGAGGTCGAGGCT A C MASTL Ensembl:ENSG00000120539 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,31158229,31158229 RNA-Seq:(High) rs1000057271 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17558923 36410 RMVar_ID_36410 Human_SNP_ID_426099288 A-to-I Human chr10 + 27183737 27183735 27183737 TTCTTTCTTTTTTTGGTTTTGGGATTTTTTTGAGACAGGATCTGGGTCTGTCGCCCAGGCTGGAA TTCTTTCTTTTTTTGGTTTTGGGATTTTTTT__GACAGGATCTGGGTCTGTCGCCCAGGCTGGAA TGA T MASTL Ensembl:ENSG00000120539 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1390602536 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_5959263 36411 RMVar_ID_36411 Human_SNP_ID_426099295 A-to-I Human chr10 - 27183772 27183770 27183773 AGAAAGTTGCAGTGAGCCGAGATTGTGCTACTACATTCCAGCCTGGGCGACAGACCCAGATCCTG AGAAAGTTGCAGTGAGCCGAGATTGTGCTAC___ATTCCAGCCTGGGCGACAGACCCAGATCCTG TGTA T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs760361716 Functional Loss DEL dbSNP153 32..34 33 - - - 36412 RMVar_ID_36412 Human_SNP_ID_426099745 A-to-I Human chr10 + 27185565 27185565 27185565 TGAGGTGGGAGAATCGCTTGAACCCGGGAGGCAGAGTTTGCAGTGAGCCGAGATTGTGCCATTGC TGAGGTGGGAGAATCGCTTGAACCCGGGAGGCGGAGTTTGCAGTGAGCCGAGATTGTGCCATTGC A G MASTL Ensembl:ENSG00000120539 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1286376896 Functional Loss SNV dbSNP153 33..33 33 - - - 36413 RMVar_ID_36413 Human_SNP_ID_426104395 A-to-I Human chr10 - 27203245 27203245 27203245 GCAGTGGCTCATGTCTATAATCCCGGGACTTTAGGAAGCTGAGATGGGTGGATTGCTTGAGCCCA GCAGTGGCTCATGTCTATAATCCCGGGACTTTCGGAAGCTGAGATGGGTGGATTGCTTGAGCCCA T G ACBD5 Ensembl:ENSG00000107897 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417855591 Functional Loss SNV dbSNP153 33..33 33 - - - 36414 RMVar_ID_36414 Human_SNP_ID_426337278 A-to-I Human chr10 - 28150026 28150026 28150026 TTCATGAAAAACTACACTACTATGAGAAGCAGAGTCCGGTGCCCATTCTCCATGGTGCGGCGGCC TTCATGAAAAACTACACTACTATGAGAAGCAGGGTCCGGTGCCCATTCTCCATGGTGCGGCGGCC T C MPP7 Ensembl:ENSG00000150054 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs754942974 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9360221 Human_Splice_Rec_1121458,Human_Splice_Rec_1121459,Human_Splice_Rec_1121490,Human_Splice_Rec_1121491,Human_Splice_Rec_1121520,Human_Splice_Rec_1121521,Human_Splice_Rec_1121556,Human_Splice_Rec_1121557,Human_Splice_Rec_1121612,Human_Splice_Rec_1121613,Human_Splice_Rec_1121624,Human_Splice_Rec_1121625 RMVar_hsa_circ_36135,RMVar_hsa_circ_80305,RMVar_hsa_circ_56504,RMVar_hsa_circ_142859,RMVar_hsa_circ_360127,RMVar_hsa_circ_142860,RMVar_hsa_circ_308712,RMVar_hsa_circ_356475,RMVar_hsa_circ_363663 36415 RMVar_ID_36415 Human_SNP_ID_426428857 A-to-I Human chr10 - 28521260 28521260 28521260 AAAATTGGCCGGGTGTGGTGGTGCATGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAAGAGA AAAATTGGCCGGGTGTGGTGGTGCATGCCTGTGATCCCAGCTACTTGGGAGGCTGAGGCAAGAGA T C WAC-AS1,WAC-AS1:2,WAC-AS1:3,WAC-AS1:4,WAC-AS1:5,WAC-AS1:6,WAC-AS1:7,WAC-AS1:8,WAC-AS1:9,WAC-AS1:10 RNACentral:URS0000D5B30D,RNACentral:URS0000D5AE7F,RNACentral:URS0000E9B485,RNACentral:URS0000D58195,RNACentral:URS0000D5DE00,RNACentral:URS0000D5A2FB,RNACentral:URS0000D5B8D9,RNACentral:URS0000D5CF18,RNACentral:URS0000759FCD,RNACentral:URS0000D5720E lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,exon,exon,exon,exon,exon,exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs563226398 Functional Loss SNV dbSNP153 33..33 33 - - - 36416 RMVar_ID_36416 Human_SNP_ID_426428867 A-to-I Human chr10 - 28521300 28521300 28521300 CCTGACCAACGTGGAGAAATTCTGTCCCTACTAAAAATGCAAAATTGGCCGGGTGTGGTGGTGCA CCTGACCAACGTGGAGAAATTCTGTCCCTACTGAAAATGCAAAATTGGCCGGGTGTGGTGGTGCA T C WAC-AS1,WAC-AS1:2,WAC-AS1:3,WAC-AS1:4,WAC-AS1:5,WAC-AS1:6,WAC-AS1:7,WAC-AS1:8,WAC-AS1:9,WAC-AS1:10 RNACentral:URS0000D5B30D,RNACentral:URS0000D5AE7F,RNACentral:URS0000E9B485,RNACentral:URS0000D58195,RNACentral:URS0000D5DE00,RNACentral:URS0000D5A2FB,RNACentral:URS0000D5B8D9,RNACentral:URS0000D5CF18,RNACentral:URS0000759FCD,RNACentral:URS0000D5720E lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,exon,exon,exon,exon,exon,exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1209613066 Functional Loss SNV dbSNP153 33..33 33 - - - 36417 RMVar_ID_36417 Human_SNP_ID_426429320 A-to-I Human chr10 - 28523105 28523105 28523105 GTGGTGGTGCGTGCCTGTGATCCCAGCTGCTCAGGAGGCTGAGGCAGGAGAATCGCTTGGACCTG GTGGTGGTGCGTGCCTGTGATCCCAGCTGCTCTGGAGGCTGAGGCAGGAGAATCGCTTGGACCTG T A WAC-AS1 Ensembl:ENSG00000254635 lincRNA exon GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1473821182 Functional Loss SNV dbSNP153 33..33 33 - - - 36418 RMVar_ID_36418 Human_SNP_ID_426429534 A-to-I Human chr10 - 28523687 28523687 28523687 GTCCCAGCTACTCGAGAGGCTAAGGCAGGAAAATCGCTTGAACCCAGGAGGCAGAGATTGCGGTG GTCCCAGCTACTCGAGAGGCTAAGGCAGGAAAGTCGCTTGAACCCAGGAGGCAGAGATTGCGGTG T C WAC-AS1 Ensembl:ENSG00000254635 lincRNA exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1259480409 Functional Loss SNV dbSNP153 33..33 33 - - - 36419 RMVar_ID_36419 Human_SNP_ID_426429535 A-to-I Human chr10 - 28523688 28523688 28523688 GGTCCCAGCTACTCGAGAGGCTAAGGCAGGAAAATCGCTTGAACCCAGGAGGCAGAGATTGCGGT GGTCCCAGCTACTCGAGAGGCTAAGGCAGGAAGATCGCTTGAACCCAGGAGGCAGAGATTGCGGT T C WAC-AS1 Ensembl:ENSG00000254635 lincRNA exon GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1208497254 Functional Loss SNV dbSNP153 33..33 33 - - - 36420 RMVar_ID_36420 Human_SNP_ID_426429902 A-to-I Human chr10 - 28525197 28525196 28525197 TGCCACCATGCCTGACCAATTTTTGTATTTTTAGTTGAGACGGGATTTTGCCATGTTGGCTAGGC TGCCACCATGCCTGACCAATTTTTGTATTTTT_GTTGAGACGGGATTTTGCCATGTTGGCTAGGC CT C WAC-AS1 Ensembl:ENSG00000254635 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1422364327 Functional Loss DEL dbSNP153 33..33 33 - - - 36421 RMVar_ID_36421 Human_SNP_ID_426429912 A-to-I Human chr10 - 28525238 28525238 28525238 CTCCTGCCTCAACCTCCCGAGTAGCTGGGATTACAGGCACTTGCCACCATGCCTGACCAATTTTT CTCCTGCCTCAACCTCCCGAGTAGCTGGGATTGCAGGCACTTGCCACCATGCCTGACCAATTTTT T C WAC-AS1 Ensembl:ENSG00000254635 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs568065870 Functional Loss SNV dbSNP153 33..33 33 - - - 36422 RMVar_ID_36422 Human_SNP_ID_426429925 A-to-I Human chr10 - 28525277 28525277 28525277 CGGCTCACAGCAACCTCCGCCTCCCGGCTTCAAGCGATTCTCCTGCCTCAACCTCCCGAGTAGCT CGGCTCACAGCAACCTCCGCCTCCCGGCTTCAGGCGATTCTCCTGCCTCAACCTCCCGAGTAGCT T C WAC-AS1 Ensembl:ENSG00000254635 lincRNA intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1171530079 Functional Loss SNV dbSNP153 33..33 33 - - - 36423 RMVar_ID_36423 Human_SNP_ID_426430038 A-to-I Human chr10 - 28525594 28525594 28525594 TGAACCTGGAAGATGGAGGTTGCAGTGAGCCAAGATCGTGCCACCTCACTCCAGCCTGGGTGATA TGAACCTGGAAGATGGAGGTTGCAGTGAGCCACGATCGTGCCACCTCACTCCAGCCTGGGTGATA T G WAC-AS1 Ensembl:ENSG00000254635 lincRNA intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1189957972 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24804307 36424 RMVar_ID_36424 Human_SNP_ID_426430039 A-to-I Human chr10 - 28525595 28525595 28525595 TTGAACCTGGAAGATGGAGGTTGCAGTGAGCCAAGATCGTGCCACCTCACTCCAGCCTGGGTGAT TTGAACCTGGAAGATGGAGGTTGCAGTGAGCCGAGATCGTGCCACCTCACTCCAGCCTGGGTGAT T C WAC-AS1 Ensembl:ENSG00000254635 lincRNA intron GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,30559470,31158229,31158229 RNA-Seq:(High) rs1013440657 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24804308 36425 RMVar_ID_36425 Human_SNP_ID_426430040 A-to-I Human chr10 - 28525599 28525599 28525599 TCGCTTGAACCTGGAAGATGGAGGTTGCAGTGAGCCAAGATCGTGCCACCTCACTCCAGCCTGGG TCGCTTGAACCTGGAAGATGGAGGTTGCAGTGCGCCAAGATCGTGCCACCTCACTCCAGCCTGGG T G WAC-AS1 Ensembl:ENSG00000254635 lincRNA intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1246879790 Functional Loss SNV dbSNP153 33..33 33 - - - 36426 RMVar_ID_36426 Human_SNP_ID_426430062 A-to-I Human chr10 - 28525686 28525686 28525686 TGAGTCAGGAGTTAGAGACCAGCAAAAAAATTAGCTGGGTGTGTTTGCGGGCACCTGTAATCCCT TGAGTCAGGAGTTAGAGACCAGCAAAAAAATTCGCTGGGTGTGTTTGCGGGCACCTGTAATCCCT T G WAC-AS1 Ensembl:ENSG00000254635 lincRNA intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1482487663 Functional Loss SNV dbSNP153 33..33 33 - - - 36427 RMVar_ID_36427 Human_SNP_ID_426430077 A-to-I Human chr10 - 28525763 28525763 28525763 AAAGATGGCTGAGGCTGGATGCTGTGGCTTATACCTGTAATCCCAGCACTTTGAGAGGCCAAGGC AAAGATGGCTGAGGCTGGATGCTGTGGCTTATGCCTGTAATCCCAGCACTTTGAGAGGCCAAGGC T C WAC-AS1 Ensembl:ENSG00000254635 lincRNA intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1220955951 Functional Loss SNV dbSNP153 33..33 33 - - - 36428 RMVar_ID_36428 Human_SNP_ID_426431264 A-to-I Human chr10 - 28530687 28530687 28530687 AAGTTAGCCAGGTGTGGTGGTGTGCGCCTGTAATCCCAGTTATTCGGGAGACTGAGGCAGGAGAA AAGTTAGCCAGGTGTGGTGGTGTGCGCCTGTATTCCCAGTTATTCGGGAGACTGAGGCAGGAGAA T A WAC-AS1 Ensembl:ENSG00000254635 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1387817646 Functional Loss SNV dbSNP153 33..33 33 - - - 36429 RMVar_ID_36429 Human_SNP_ID_426431625 A-to-I Human chr10 - 28531913 28531913 28531913 CTCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCGCTCGGCTTTTCACC CTCCCGCCTCGGCCTCCCAAAGTGCTGGGATTGCAGGCGTGAGCCACTGCGCTCGGCTTTTCACC T C WAC-AS1 Ensembl:ENSG00000254635 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1181039063 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24804335 36430 RMVar_ID_36430 Human_SNP_ID_426434242 A-to-I Human chr10 + 28538357 28538357 28538357 GAATCTCAGCACTTTGGGAGGCCGAGGCAGGCAGATCACCTGAGGTCAGGAGTTTGAGACCAGCC GAATCTCAGCACTTTGGGAGGCCGAGGCAGGCGGATCACCTGAGGTCAGGAGTTTGAGACCAGCC A G WAC Ensembl:ENSG00000095787 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1399214574 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 36431 RMVar_ID_36431 Human_SNP_ID_426434255 A-to-I Human chr10 + 28538395 28538395 28538395 CCTGAGGTCAGGAGTTTGAGACCAGCCTGGCCAACGTGGTGAAACCCTGTCTCTACTACAAATAC CCTGAGGTCAGGAGTTTGAGACCAGCCTGGCCGACGTGGTGAAACCCTGTCTCTACTACAAATAC A G WAC Ensembl:ENSG00000095787 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1306167257 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 36432 RMVar_ID_36432 Human_SNP_ID_426434270 A-to-I Human chr10 + 28538435 28538435 28538435 GAAACCCTGTCTCTACTACAAATACAAAAGTTAGCTGGTTGCGGTGGCGAGTGCCTGTAATCCCA GAAACCCTGTCTCTACTACAAATACAAAAGTTGGCTGGTTGCGGTGGCGAGTGCCTGTAATCCCA A G WAC Ensembl:ENSG00000095787 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1137213 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23451873 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 36433 RMVar_ID_36433 Human_SNP_ID_426434299 A-to-I Human chr10 + 28538532 28538532 28538532 TGAACCCAGGAGGTGGAGGTTGCAGTGAGCTGAGATTGTGCCATTGCACTCCAGCCTGGGAGACG TGAACCCAGGAGGTGGAGGTTGCAGTGAGCTGGGATTGTGCCATTGCACTCCAGCCTGGGAGACG A G WAC Ensembl:ENSG00000095787 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1364525574 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9621389,Human_RBP_ID_22887403,Human_RBP_ID_24804423 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 36434 RMVar_ID_36434 Human_SNP_ID_426434680 A-to-I Human chr10 + 28539557 28539557 28539557 ACCAAAAGCAAAAACCTTAAGGTACAATCGTTAGGGTTTGTTTTTTGGTTTTTTTTTTTCTGGAG ACCAAAAGCAAAAACCTTAAGGTACAATCGTTGGGGTTTGTTTTTTGGTTTTTTTTTTTCTGGAG A G WAC Ensembl:ENSG00000095787 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1138608 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_376390,Human_RBP_ID_3347568,Human_RBP_ID_5960708,Human_RBP_ID_23451889 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 36435 RMVar_ID_36435 Human_SNP_ID_426434725 A-to-I Human chr10 + 28539676 28539676 28539676 TGCCTCCTGAGTTCAAGCGATCCTTCTGCCTTAATGTCCCAAGTAGCTGGGATTACAAACATACG TGCCTCCTGAGTTCAAGCGATCCTTCTGCCTTGATGTCCCAAGTAGCTGGGATTACAAACATACG A G WAC Ensembl:ENSG00000095787 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1450402779 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1351700 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 36436 RMVar_ID_36436 Human_SNP_ID_426434746 A-to-I Human chr10 + 28539742 28539742 28539742 CATCATGCCCGGCTAATTTTTGTATTTTTAGTAGAAATAGGGTTTCACCAAGTTGGCCAGGCTGG CATCATGCCCGGCTAATTTTTGTATTTTTAGTGGAAATAGGGTTTCACCAAGTTGGCCAGGCTGG A G WAC Ensembl:ENSG00000095787 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs775636335 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 36437 RMVar_ID_36437 Human_SNP_ID_426434759 A-to-I Human chr10 + 28539793 28539793 28539793 GTTGGCCAGGCTGGTCTCAATCTCCTGCTCTCAAGTGATCCACCTGCCTCGGCCTCCCAAAGTGC GTTGGCCAGGCTGGTCTCAATCTCCTGCTCTCGAGTGATCCACCTGCCTCGGCCTCCCAAAGTGC A G WAC Ensembl:ENSG00000095787 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1417743644 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 36438 RMVar_ID_36438 Human_SNP_ID_426436140 A-to-I Human chr10 + 28544048 28544048 28544048 GGGATTACAGGTGCGCACTGCCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTTG GGGATTACAGGTGCGCACTGCCACGCCCAGCTGATTTTTGTATTTTTAGTAGAGACAGGGTTTTG A G WAC Ensembl:ENSG00000095787 Protein coding intron GSE107867 ASD brains,cerebellum;ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs778830867 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 36439 RMVar_ID_36439 Human_SNP_ID_426437585 A-to-I Human chr10 + 28548998 28548998 28548998 CTCACTGCAGCCTCAAAAAAACTCCTGGGCTCAAGTGATCCTCTTGCCACAACCTCCCAAGTAGT CTCACTGCAGCCTCAAAAAAACTCCTGGGCTCCAGTGATCCTCTTGCCACAACCTCCCAAGTAGT A C WAC Ensembl:ENSG00000095787 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,cerebellum - 29129909,30559470 RNA-Seq:(High) rs1423979423 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8332710 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 36440 RMVar_ID_36440 Human_SNP_ID_426437853 A-to-I Human chr10 + 28549994 28549994 28549994 AGACCAGCCAGGCCAAACATGGTTGAAACCCTATCTCTACTAAAAATACAAAAAGTTAGCTGGGT AGACCAGCCAGGCCAAACATGGTTGAAACCCTGTCTCTACTAAAAATACAAAAAGTTAGCTGGGT A G WAC Ensembl:ENSG00000095787 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs369888810 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 36441 RMVar_ID_36441 Human_SNP_ID_426437860 A-to-I Human chr10 + 28550009 28550009 28550009 AACATGGTTGAAACCCTATCTCTACTAAAAATACAAAAAGTTAGCTGGGTGTGGTGGCCAGCACC AACATGGTTGAAACCCTATCTCTACTAAAAATGCAAAAAGTTAGCTGGGTGTGGTGGCCAGCACC A G WAC Ensembl:ENSG00000095787 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1338351168 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19507064 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 36442 RMVar_ID_36442 Human_SNP_ID_426437877 A-to-I Human chr10 + 28550075 28550075 28550075 GTAATCCCAGCTACTCGGGAGGCTGATGAGGCAGGAGAATCGCTTGAACTTGGGAGATGGAGGTC GTAATCCCAGCTACTCGGGAGGCTGATGAGGCGGGAGAATCGCTTGAACTTGGGAGATGGAGGTC A G WAC Ensembl:ENSG00000095787 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,frontal_cortex - 29129909,30559470 RNA-Seq:(High) rs924680532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11343372 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 36443 RMVar_ID_36443 Human_SNP_ID_426441335 A-to-I Human chr10 + 28562174 28562174 28562174 TGCCTCCTGAGTTCAAGTGATTCTCCTGCCTCAACTTCCTGAGTAGCTGGGATTGTAGGTGTGCG TGCCTCCTGAGTTCAAGTGATTCTCCTGCCTCGACTTCCTGAGTAGCTGGGATTGTAGGTGTGCG A G WAC Ensembl:ENSG00000095787 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1390963447 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 36444 RMVar_ID_36444 Human_SNP_ID_426441350 A-to-I Human chr10 + 28562229 28562229 28562229 TAGGTGTGCGCAACCACATCTGGCTAATTTTTATATTTTTAGTAGAGACGGGGTTTCACCATGTT TAGGTGTGCGCAACCACATCTGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTT A G WAC Ensembl:ENSG00000095787 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1260428992 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 36445 RMVar_ID_36445 Human_SNP_ID_426441351 A-to-I Human chr10 + 28562229 28562229 28562229 TAGGTGTGCGCAACCACATCTGGCTAATTTTTATATTTTTAGTAGAGACGGGGTTTCACCATGTT TAGGTGTGCGCAACCACATCTGGCTAATTTTTTTATTTTTAGTAGAGACGGGGTTTCACCATGTT A T WAC Ensembl:ENSG00000095787 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1260428992 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 36446 RMVar_ID_36446 Human_SNP_ID_426441874 A-to-I Human chr10 + 28563860 28563860 28563860 CTGACCTCGTGATCCGCTGCCTTGGTCTCCCAAAGTGCTGGAATTAAAAGCGTGAGCCACTGTGC CTGACCTCGTGATCCGCTGCCTTGGTCTCCCACAGTGCTGGAATTAAAAGCGTGAGCCACTGTGC A C WAC Ensembl:ENSG00000095787 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1257950367 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 36447 RMVar_ID_36447 Human_SNP_ID_426441875 A-to-I Human chr10 + 28563860 28563860 28563860 CTGACCTCGTGATCCGCTGCCTTGGTCTCCCAAAGTGCTGGAATTAAAAGCGTGAGCCACTGTGC CTGACCTCGTGATCCGCTGCCTTGGTCTCCCAGAGTGCTGGAATTAAAAGCGTGAGCCACTGTGC A G WAC Ensembl:ENSG00000095787 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1257950367 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 36448 RMVar_ID_36448 Human_SNP_ID_426441947 A-to-I Human chr10 + 28564161 28564161 28564161 GTGGTGTACACCTGTAGTCCCAGCAACTCTGGAGGCTGAGGTGGGAGGAAGGCTTAAGCCTAGGA GTGGTGTACACCTGTAGTCCCAGCAACTCTGGTGGCTGAGGTGGGAGGAAGGCTTAAGCCTAGGA A T WAC Ensembl:ENSG00000095787 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs563771500 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 36449 RMVar_ID_36449 Human_SNP_ID_426441950 A-to-I Human chr10 + 28564206 28564206 28564206 AGGAAGGCTTAAGCCTAGGAGGTGGAGGTTGCAATGAGCCAAGATTGTGCCACTGCACGATAGAG AGGAAGGCTTAAGCCTAGGAGGTGGAGGTTGCCATGAGCCAAGATTGTGCCACTGCACGATAGAG A C WAC Ensembl:ENSG00000095787 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1397788669 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 36450 RMVar_ID_36450 Human_SNP_ID_426443122 A-to-I Human chr10 + 28568467 28568467 28568467 CAGTGGCACGGTCTTGGCTCGCTGCAACCTCCACCTCCCGGGTTCAAGCAATTTTCCTGTCTCAG CAGTGGCACGGTCTTGGCTCGCTGCAACCTCCGCCTCCCGGGTTCAAGCAATTTTCCTGTCTCAG A G WAC Ensembl:ENSG00000095787 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1370133923 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11344236 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 36451 RMVar_ID_36451 Human_SNP_ID_426445670 A-to-I Human chr10 + 28578012 28578012 28578012 AAGTGAACGTCTCTACTAAAAATACAAAAATTAGTGGGACATGGTAGCGTATATCTGTAGTGCCA AAGTGAACGTCTCTACTAAAAATACAAAAATTGGTGGGACATGGTAGCGTATATCTGTAGTGCCA A G WAC Ensembl:ENSG00000095787 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1366401864 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11344636 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 36452 RMVar_ID_36452 Human_SNP_ID_426454242 A-to-I Human chr10 + 28609191 28609191 28609191 TGAAACCAGCCTGACCAAGATGGTGAAACGCTATCTCTAATAAAAATACAAAAGTTAACCAGGCG TGAAACCAGCCTGACCAAGATGGTGAAACGCTGTCTCTAATAAAAATACAAAAGTTAACCAGGCG A G WAC Ensembl:ENSG00000095787 Protein coding intron GSE38233;GSE100210;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,frontal_cortex - 24183664,29129909,30559470 RNA-Seq:(High) rs1413023065 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_376421,Human_RBP_ID_5961771 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_352921,RMVar_hsa_circ_103059,RMVar_hsa_circ_29550,RMVar_hsa_circ_142872,RMVar_hsa_circ_53960,RMVar_hsa_circ_331927 36453 RMVar_ID_36453 Human_SNP_ID_426454407 A-to-I Human chr10 + 28609753 28609753 28609753 AAACTTAGCCAGGTGTGGTGGTGAACGCCTGTAGTTCCAGCTACTTGGGAGGCTGAGGTGGGAGA AAACTTAGCCAGGTGTGGTGGTGAACGCCTGTTGTTCCAGCTACTTGGGAGGCTGAGGTGGGAGA A T WAC Ensembl:ENSG00000095787 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1456538160 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24805166 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_352921,RMVar_hsa_circ_103059,RMVar_hsa_circ_29550,RMVar_hsa_circ_142872,RMVar_hsa_circ_53960,RMVar_hsa_circ_331927 36454 RMVar_ID_36454 Human_SNP_ID_426454530 A-to-I Human chr10 + 28610167 28610167 28610167 GTTGGGCAGGCTGCTCTTGAACTCCTAACCTTAGGCGATCCACCTGCCTCAGCCTCCCAAAGTGC GTTGGGCAGGCTGCTCTTGAACTCCTAACCTTGGGCGATCCACCTGCCTCAGCCTCCCAAAGTGC A G WAC Ensembl:ENSG00000095787 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs371888776 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11345622 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_352921,RMVar_hsa_circ_103059,RMVar_hsa_circ_29550,RMVar_hsa_circ_142872,RMVar_hsa_circ_53960,RMVar_hsa_circ_331927 36455 RMVar_ID_36455 Human_SNP_ID_426455338 A-to-I Human chr10 + 28613021 28613020 28613021 CTCCTTTAAGAAGGCTGGGCGCGGTGGCTCACAGCTATAATTACAGCACTTAGGAGGCCAAGGCA CTCCTTTAAGAAGGCTGGGCGCGGTGGCTCAC_GCTATAATTACAGCACTTAGGAGGCCAAGGCA CA C WAC Ensembl:ENSG00000095787 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1286532484 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_24805208 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 36456 RMVar_ID_36456 Human_SNP_ID_426455398 A-to-I Human chr10 + 28613202 28613202 28613202 CAAGCCTGGCCAACAGGCAAAACCCGGTCTCTACTAAAAGTACAAAAATTATCTGGGTGTGCTGG CAAGCCTGGCCAACAGGCAAAACCCGGTCTCTGCTAAAAGTACAAAAATTATCTGGGTGTGCTGG A G WAC Ensembl:ENSG00000095787 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1400932398 Functional Loss SNV dbSNP153 33..33 33 - - - 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 36457 RMVar_ID_36457 Human_SNP_ID_426455410 A-to-I Human chr10 + 28613246 28613246 28613246 AAAATTATCTGGGTGTGCTGGCACAGACCTATAATCCCAGCTACTCGGGCGGCTGAGGCATGAGA AAAATTATCTGGGTGTGCTGGCACAGACCTATGATCCCAGCTACTCGGGCGGCTGAGGCATGAGA A G WAC Ensembl:ENSG00000095787 Protein coding intron GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-Seq:(High) rs982856254 Functional Loss SNV dbSNP153 33..33 33 - - - 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 36458 RMVar_ID_36458 Human_SNP_ID_426455694 A-to-I Human chr10 + 28614271 28614271 28614271 GGGACTACAGGCGCCCGCCACTGCGCCCGGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTC GGGACTACAGGCGCCCGCCACTGCGCCCGGCTCATTTTTTGTATTTTTAGTAGAGACGGGGTTTC A C WAC Ensembl:ENSG00000095787 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1028637971 Functional Loss SNV dbSNP153 33..33 33 - - - 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 36459 RMVar_ID_36459 Human_SNP_ID_426455695 A-to-I Human chr10 + 28614271 28614271 28614271 GGGACTACAGGCGCCCGCCACTGCGCCCGGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTC GGGACTACAGGCGCCCGCCACTGCGCCCGGCTGATTTTTTGTATTTTTAGTAGAGACGGGGTTTC A G WAC Ensembl:ENSG00000095787 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1028637971 Functional Loss SNV dbSNP153 33..33 33 - - - 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 36460 RMVar_ID_36460 Human_SNP_ID_426509122 A-to-I Human chr10 - 28816779 28816779 28816779 AACCTCTGCCTCCAAGTTTAAGCGATTATCCTACCTCAGCCTCCCAAGTAGCTGGGATTACAGGC AACCTCTGCCTCCAAGTTTAAGCGATTATCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs547952218 Functional Loss SNV dbSNP153 33..33 33 - - - 36461 RMVar_ID_36461 Human_SNP_ID_426660996 A-to-I Human chr10 + 29419353 29419353 29419353 TTTTGTATTTTTAGTAGAGATGGGGTTTCACCAGTTTGCCCAAGCTGGTCTCGAACTCCTAGGCT TTTTGTATTTTTAGTAGAGATGGGGTTTCACCGGTTTGCCCAAGCTGGTCTCGAACTCCTAGGCT A G SVIL-AS1 Ensembl:ENSG00000224597 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1313808642 Functional Loss SNV dbSNP153 33..33 33 - - - 36462 RMVar_ID_36462 Human_SNP_ID_426671543 A-to-I Human chr10 + 29458846 29458846 29458846 TGGTATTTTTTGAGACAAGGTCTCACTCTGCTACTCAGGCTGGAGTGCAGTGGTGCAATCATAGC TGGTATTTTTTGAGACAAGGTCTCACTCTGCTGCTCAGGCTGGAGTGCAGTGGTGCAATCATAGC A G SVIL-AS1 Ensembl:ENSG00000224597 Pseudogene intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1374605282 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_142881 36463 RMVar_ID_36463 Human_SNP_ID_426671628 A-to-I Human chr10 + 29459179 29459179 29459179 TAACCCAGGCTGGAGGGCAGTGGCTCAATCATAGCTCTCTGCAGCCTTAAACTCCTGGACTCAAG TAACCCAGGCTGGAGGGCAGTGGCTCAATCATGGCTCTCTGCAGCCTTAAACTCCTGGACTCAAG A G SVIL-AS1 Ensembl:ENSG00000224597 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1135040 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11346370 RMVar_hsa_circ_142881 36464 RMVar_ID_36464 Human_SNP_ID_426671633 A-to-I Human chr10 + 29459195 29459195 29459195 GCAGTGGCTCAATCATAGCTCTCTGCAGCCTTAAACTCCTGGACTCAAGCAGTCCTCCCACCTCA GCAGTGGCTCAATCATAGCTCTCTGCAGCCTTGAACTCCTGGACTCAAGCAGTCCTCCCACCTCA A G SVIL-AS1 Ensembl:ENSG00000224597 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1135039 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9588670,Human_RBP_ID_11346370 RMVar_hsa_circ_142881 36465 RMVar_ID_36465 Human_SNP_ID_426672009 A-to-I Human chr10 + 29460795 29460795 29460795 AGGCATTATGGTGTGTGCTTGTAGTCCCAGCTACCTGGGAGGCTGATGTGGGAGGATTGTCTGAG AGGCATTATGGTGTGTGCTTGTAGTCCCAGCTTCCTGGGAGGCTGATGTGGGAGGATTGTCTGAG A T SVIL-AS1 Ensembl:ENSG00000224597 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909946860 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17346640 36466 RMVar_ID_36466 Human_SNP_ID_426672012 A-to-I Human chr10 - 29460798 29460798 29460798 AGGCTCAGACAATCCTCCCACATCAGCCTCCCAGGTAGCTGGGACTACAAGCACACACCATAATG AGGCTCAGACAATCCTCCCACATCAGCCTCCCCGGTAGCTGGGACTACAAGCACACACCATAATG T G SVIL Ensembl:ENSG00000197321 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs548143588 Functional Loss SNV dbSNP153 33..33 33 - - - 36467 RMVar_ID_36467 Human_SNP_ID_426688866 A-to-I Human chr10 - 29527494 29527494 29527494 TGACCCCGGGAGGCGGAGTTTGCAGTGAGCCAAGATCATGCCACTGCACTCCAGCCTGGTGACAG TGACCCCGGGAGGCGGAGTTTGCAGTGAGCCAGGATCATGCCACTGCACTCCAGCCTGGTGACAG T C SVIL Ensembl:ENSG00000197321 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs894445871 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_15950,RMVar_hsa_circ_18215,RMVar_hsa_circ_334511,RMVar_hsa_circ_331556,RMVar_hsa_circ_32975,RMVar_hsa_circ_142887,RMVar_hsa_circ_72217,RMVar_hsa_circ_142886,RMVar_hsa_circ_18678,RMVar_hsa_circ_362967,RMVar_hsa_circ_123646 36468 RMVar_ID_36468 Human_SNP_ID_426688868 A-to-I Human chr10 - 29527499 29527499 29527499 TCACTTGACCCCGGGAGGCGGAGTTTGCAGTGAGCCAAGATCATGCCACTGCACTCCAGCCTGGT TCACTTGACCCCGGGAGGCGGAGTTTGCAGTGGGCCAAGATCATGCCACTGCACTCCAGCCTGGT T C SVIL Ensembl:ENSG00000197321 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1214321914 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_15950,RMVar_hsa_circ_18215,RMVar_hsa_circ_334511,RMVar_hsa_circ_331556,RMVar_hsa_circ_32975,RMVar_hsa_circ_142887,RMVar_hsa_circ_72217,RMVar_hsa_circ_142886,RMVar_hsa_circ_18678,RMVar_hsa_circ_362967,RMVar_hsa_circ_123646 36469 RMVar_ID_36469 Human_SNP_ID_426688869 A-to-I Human chr10 - 29527503 29527503 29527503 AGAATCACTTGACCCCGGGAGGCGGAGTTTGCAGTGAGCCAAGATCATGCCACTGCACTCCAGCC AGAATCACTTGACCCCGGGAGGCGGAGTTTGCCGTGAGCCAAGATCATGCCACTGCACTCCAGCC T G SVIL Ensembl:ENSG00000197321 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1337811923 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_15950,RMVar_hsa_circ_18215,RMVar_hsa_circ_334511,RMVar_hsa_circ_331556,RMVar_hsa_circ_32975,RMVar_hsa_circ_142887,RMVar_hsa_circ_72217,RMVar_hsa_circ_142886,RMVar_hsa_circ_18678,RMVar_hsa_circ_362967,RMVar_hsa_circ_123646 36470 RMVar_ID_36470 Human_SNP_ID_426688885 A-to-I Human chr10 - 29527551 29527551 29527551 GTGGTGGTGCGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGACCCCG GTGGTGGTGCGCGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGACCCCG T C SVIL Ensembl:ENSG00000197321 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs922323346 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_15950,RMVar_hsa_circ_18215,RMVar_hsa_circ_334511,RMVar_hsa_circ_331556,RMVar_hsa_circ_32975,RMVar_hsa_circ_142887,RMVar_hsa_circ_72217,RMVar_hsa_circ_142886,RMVar_hsa_circ_18678,RMVar_hsa_circ_362967,RMVar_hsa_circ_123646 36471 RMVar_ID_36471 Human_SNP_ID_426705788 A-to-I Human chr10 - 29596249 29596249 29596249 TTACACTGGTCTCAAACTCCTGGCCTCAAGCAATCCTCCCACCTCGGCCTCCCAAAGGGCTGGGA TTACACTGGTCTCAAACTCCTGGCCTCAAGCAGTCCTCCCACCTCGGCCTCCCAAAGGGCTGGGA T C SVIL Ensembl:ENSG00000197321 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs892443848 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22771,RMVar_hsa_circ_64840,RMVar_hsa_circ_107890,RMVar_hsa_circ_142889,RMVar_hsa_circ_118204,RMVar_hsa_circ_298698,RMVar_hsa_circ_142891 36472 RMVar_ID_36472 Human_SNP_ID_458109443 A-to-I Human chr11 + 20007050 20007049 20007051 ACAATCTCAGCTCACTGCAACCTCCGCCTCCCAGGCTCAAACAATCCTCCCACCTCAGCCTCCAG ACAATCTCAGCTCACTGCAACCTCCGCCTCCC__GCTCAAACAATCCTCCCACCTCAGCCTCCAG CAG C NAV2 Ensembl:ENSG00000166833 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1309710334 Functional Loss DEL dbSNP153 33..34 33 - - - 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_280789,RMVar_hsa_circ_148666 36473 RMVar_ID_36473 Human_SNP_ID_458198472 A-to-I Human chr11 + 20365241 20365241 20365241 GAACTCTTGACCTCAGATGATGCTCCCGCTTCAGCCTCCCAAAGTGCTGCGATTACAGGCGTGAG GAACTCTTGACCTCAGATGATGCTCCCGCTTCGGCCTCCCAAAGTGCTGCGATTACAGGCGTGAG A G HTATIP2 Ensembl:ENSG00000109854 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1422973451 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57003,RMVar_hsa_circ_107336,RMVar_hsa_circ_148687,RMVar_hsa_circ_358048 36474 RMVar_ID_36474 Human_SNP_ID_458204523 A-to-I Human chr11 + 20390070 20390070 20390070 CTGCTCAGAAGACTGAGGCAGGTGAATTGCTTAAACCTGGGAGGCAGAGGTGGCAGTGAGCTGAG CTGCTCAGAAGACTGAGGCAGGTGAATTGCTTCAACCTGGGAGGCAGAGGTGGCAGTGAGCTGAG A C PRMT3 Ensembl:ENSG00000185238 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1349400797 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_438,RMVar_hsa_circ_63978,RMVar_hsa_circ_110608,RMVar_hsa_circ_40294,RMVar_hsa_circ_16408,RMVar_hsa_circ_63176,RMVar_hsa_circ_148688,RMVar_hsa_circ_350084,RMVar_hsa_circ_23469 36475 RMVar_ID_36475 Human_SNP_ID_458204739 A-to-I Human chr11 + 20390839 20390839 20390839 TTGGGAGGCCAAGGCGGATGGATCACAAGGTCAGGAGATCGAGACCATCCTGGCTAACCCAGTGA TTGGGAGGCCAAGGCGGATGGATCACAAGGTCGGGAGATCGAGACCATCCTGGCTAACCCAGTGA A G PRMT3 Ensembl:ENSG00000185238 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1314178374 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_438,RMVar_hsa_circ_63978,RMVar_hsa_circ_110608,RMVar_hsa_circ_40294,RMVar_hsa_circ_16408,RMVar_hsa_circ_63176,RMVar_hsa_circ_148688,RMVar_hsa_circ_350084,RMVar_hsa_circ_23469 36476 RMVar_ID_36476 Human_SNP_ID_458212668 A-to-I Human chr11 + 20421151 20421151 20421151 GCCTTGACCTCCCAGGCCCAAGTGATCCTCCTACCTTGCTTCTCGAGTAGCCGGGACCACAGGCT GCCTTGACCTCCCAGGCCCAAGTGATCCTCCTGCCTTGCTTCTCGAGTAGCCGGGACCACAGGCT A G PRMT3 Ensembl:ENSG00000185238 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1207677312 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_30755,RMVar_hsa_circ_63978,RMVar_hsa_circ_40294,RMVar_hsa_circ_16408,RMVar_hsa_circ_29981,RMVar_hsa_circ_148690,RMVar_hsa_circ_148693,RMVar_hsa_circ_17828,RMVar_hsa_circ_351387,RMVar_hsa_circ_48763,RMVar_hsa_circ_148694,RMVar_hsa_circ_297212,RMVar_hsa_circ_343148,RMVar_hsa_circ_344494,RMVar_hsa_circ_3094,RMVar_hsa_circ_62938,RMVar_hsa_circ_148696,RMVar_hsa_circ_22584,RMVar_hsa_circ_148697,RMVar_hsa_circ_148695,RMVar_hsa_circ_148702,RMVar_hsa_circ_271119,RMVar_hsa_circ_302709,RMVar_hsa_circ_273715,RMVar_hsa_circ_71041,RMVar_hsa_circ_148705,RMVar_hsa_circ_148706,RMVar_hsa_circ_148707,RMVar_hsa_circ_148704,RMVar_hsa_circ_148708,RMVar_hsa_circ_283553,RMVar_hsa_circ_358719,RMVar_hsa_circ_362639,RMVar_hsa_circ_301828,RMVar_hsa_circ_148709 36477 RMVar_ID_36477 Human_SNP_ID_458235221 A-to-I Human chr11 + 20513190 20513190 20513190 CTCCCACCTCAGCCTCCCTAATAGCTGGGACTACAGGCACATGCCACCACACCTGGGTAATTTTT CTCCCACCTCAGCCTCCCTAATAGCTGGGACTGCAGGCACATGCCACCACACCTGGGTAATTTTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1284364985 Functional Loss SNV dbSNP153 33..33 33 - - - 36478 RMVar_ID_36478 Human_SNP_ID_460040582 A-to-I Human chr11 - 27331855 27331855 27331855 CATTAATGTCCTTAAAGATGAGGAAAAACACTACATCCATACTGTCCTAACTCCAGTACTCTCCT CATTAATGTCCTTAAAGATGAGGAAAAACACTGCATCCATACTGTCCTAACTCCAGTACTCTCCT T C CCDC34 Ensembl:ENSG00000109881 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232941713 Functional Loss SNV dbSNP153 33..33 33 - - - 36479 RMVar_ID_36479 Human_SNP_ID_460064358 A-to-I Human chr11 - 27435577 27435577 27435577 AGGCTGAGGCAGGAGAATAGCTTGAACCCAGGAGGCGGAGGTTGCAGTGAACCGAGATTGCACCA AGGCTGAGGCAGGAGAATAGCTTGAACCCAGGGGGCGGAGGTTGCAGTGAACCGAGATTGCACCA T C LGR4 Ensembl:ENSG00000205213 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1426907094 Functional Loss SNV dbSNP153 33..33 33 - - - 36480 RMVar_ID_36480 Human_SNP_ID_460068702 A-to-I Human chr11 - 27454717 27454717 27454717 TGCTCTGTCTTCCAGGCTAGAGAGCAGGTGGCATGATCTCGGCTCACTGCAACCACCACCGCCCT TGCTCTGTCTTCCAGGCTAGAGAGCAGGTGGCCTGATCTCGGCTCACTGCAACCACCACCGCCCT T G LGR4 Ensembl:ENSG00000205213 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs921983382 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11585874 36481 RMVar_ID_36481 Human_SNP_ID_460075837 A-to-I Human chr11 - 27484075 27484075 27484075 CAGTCTTCTGATGGCGACTTTACCGTGACAGCAGAAGTGGTATTGTAGGTCCAGGCACTGCCAGC CAGTCTTCTGATGGCGACTTTACCGTGACAGCGGAAGTGGTATTGTAGGTCCAGGCACTGCCAGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879076927 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11586187 36482 RMVar_ID_36482 Human_SNP_ID_460169787 A-to-I Human chr11 - 27890774 27890774 27890774 GCATATTAACCTTATACCAAACAAACAAGATCAAACTCTCACTATTGTGGATACTGGAATTGGAA GCATATTAACCTTATACCAAACAAACAAGATCGAACTCTCACTATTGTGGATACTGGAATTGGAA T C HSP90AA2P Ensembl:ENSG00000224411 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215276056 Functional Loss SNV dbSNP153 33..33 33 - - - 36483 RMVar_ID_36483 Human_SNP_ID_460313216 A-to-I Human chr11 + 28460283 28460283 28460283 TGTAATGGACATTTGTCATTTTTCTTACCAATATCTATTTCTACCTACTTGAGTAATCAGAAACA TGTAATGGACATTTGTCATTTTTCTTACCAATGTCTATTTCTACCTACTTGAGTAATCAGAAACA A G METTL15 Ensembl:ENSG00000169519 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1471819729 Functional Loss SNV dbSNP153 33..33 33 - - - 36484 RMVar_ID_36484 Human_SNP_ID_33306086 A-to-I Human chr1 - 150046495 150046495 150046495 TGCAGTGAGCCGAGATCGCCCCACTGTACTCCAGCCTGGGTGACAGAGCAAGACTCTGTCTCAAA TGCAGTGAGCCGAGATCGCCCCACTGTACTCCCGCCTGGGTGACAGAGCAAGACTCTGTCTCAAA T G AC244033.2 Ensembl:ENSG00000285184 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs367638615 Functional Loss SNV dbSNP153 33..33 33 - - - 36485 RMVar_ID_36485 Human_SNP_ID_33306217 A-to-I Human chr1 - 150046943 150046943 150046943 CCTTAGCCTCCCCAGTAGCTGGGATTACAGGCACCTGCCACCATGTCCAATTAATTTTTGTATTT CCTTAGCCTCCCCAGTAGCTGGGATTACAGGCGCCTGCCACCATGTCCAATTAATTTTTGTATTT T C AC244033.2 Ensembl:ENSG00000285184 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1305792091 Functional Loss SNV dbSNP153 33..33 33 - - - 36486 RMVar_ID_36486 Human_SNP_ID_33306253 A-to-I Human chr1 - 150047065 150047065 150047065 TGAGGATATTGACTTTGTTTTTTTTCCAAGACAGAGCTGTGCTCTGTCGCCCAGGCTAGAGTGCA TGAGGATATTGACTTTGTTTTTTTTCCAAGACGGAGCTGTGCTCTGTCGCCCAGGCTAGAGTGCA T C AC244033.2 Ensembl:ENSG00000285184 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1389274065 Functional Loss SNV dbSNP153 33..33 33 - - - 36487 RMVar_ID_36487 Human_SNP_ID_33306422 A-to-I Human chr1 - 150047892 150047892 150047892 GAGTGCACGCTGGAGCGCGATCTTGTCTTACTACAACCTCTGCCTCCCAGATTCAAGCGATTTTC GAGTGCACGCTGGAGCGCGATCTTGTCTTACTGCAACCTCTGCCTCCCAGATTCAAGCGATTTTC T C AC244033.2 Ensembl:ENSG00000285184 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910546906 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_125548,Human_Splice_Rec_125556,Human_Splice_Rec_125562 36488 RMVar_ID_36488 Human_SNP_ID_33313918 A-to-I Human chr1 + 150079470 150079470 150079470 TCTCTCTCTGTCACCCAGATTGGCGTGATCTCAGCTCACTGCAACCTCCGCCTCCCAGGTTCAAG TCTCTCTCTGTCACCCAGATTGGCGTGATCTCTGCTCACTGCAACCTCCGCCTCCCAGGTTCAAG A T VPS45 Ensembl:ENSG00000136631 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs902532497 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6693,RMVar_hsa_circ_293143,RMVar_hsa_circ_62762,RMVar_hsa_circ_61631,RMVar_hsa_circ_11465,RMVar_hsa_circ_42942,RMVar_hsa_circ_284350,RMVar_hsa_circ_359182,RMVar_hsa_circ_9949,RMVar_hsa_circ_3989,RMVar_hsa_circ_284279,RMVar_hsa_circ_323920 36489 RMVar_ID_36489 Human_SNP_ID_33317824 A-to-I Human chr1 + 150097462 150097462 150097462 CTGTATAATCCTGGGTGCAGTGGTTTATGCCTATAATCCCAGCACTTTGGGAGGCCGAGCGGGCA CTGTATAATCCTGGGTGCAGTGGTTTATGCCTCTAATCCCAGCACTTTGGGAGGCCGAGCGGGCA A C VPS45 Ensembl:ENSG00000136631 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1052725110 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 36490 RMVar_ID_36490 Human_SNP_ID_33318243 A-to-I Human chr1 + 150099333 150099332 150099333 CCTGGCCAACATAGTGAAACCTTGTCTCTACTAAAAAAAAAAATACAAAAATTAGCCGGGTGTGG CCTGGCCAACATAGTGAAACCTTGTCTCTACT_AAAAAAAAAATACAAAAATTAGCCGGGTGTGG TA T VPS45 Ensembl:ENSG00000136631 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1181008396 Functional Loss DEL 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 36491 RMVar_ID_36491 Human_SNP_ID_33320165 A-to-I Human chr1 + 150107762 150107762 150107762 GTCTCTATTAAAAATACAAAAAGTAGTCTGGCATGGTGGCGCACGCCTGTATTCCCAGCTACTTA GTCTCTATTAAAAATACAAAAAGTAGTCTGGCGTGGTGGCGCACGCCTGTATTCCCAGCTACTTA A G VPS45 Ensembl:ENSG00000136631 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs782025825 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 36492 RMVar_ID_36492 Human_SNP_ID_33322431 A-to-I Human chr1 + 150117803 150117803 150117803 ATCGCTTGAGTCCGGGAGGCGGAGGCTGTAGTAAGCTGAGATCGTACCACTGCACTCCAGCCTGG ATCGCTTGAGTCCGGGAGGCGGAGGCTGTAGTGAGCTGAGATCGTACCACTGCACTCCAGCCTGG A G VPS45 Ensembl:ENSG00000136631 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1553808723 Functional Loss SNV dbSNP153 33..33 33 - - - 36493 RMVar_ID_36493 Human_SNP_ID_33323986 A-to-I Human chr1 + 150124660 150124660 150124660 ACCCCCCTACCTCCCGGATTTAAGTAATTCTCATGCCTCAGCCTCCCAAGTAGCTGGGACTACAA ACCCCCCTACCTCCCGGATTTAAGTAATTCTCGTGCCTCAGCCTCCCAAGTAGCTGGGACTACAA A G VPS45 Ensembl:ENSG00000136631 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404785445 Functional Loss SNV dbSNP153 33..33 33 - - - 36494 RMVar_ID_36494 Human_SNP_ID_33324252 A-to-I Human chr1 + 150125737 150125737 150125737 TTTGAGATGGAGTCTCCTCTGTTGCCCAGGCTAGAGTGCAGTGATGTGATCTCAGCTCACTGTAA TTTGAGATGGAGTCTCCTCTGTTGCCCAGGCTGGAGTGCAGTGATGTGATCTCAGCTCACTGTAA A G VPS45 Ensembl:ENSG00000136631 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1274613511 Functional Loss SNV dbSNP153 33..33 33 - - - 36495 RMVar_ID_36495 Human_SNP_ID_33324257 A-to-I Human chr1 + 150125788 150125781 150125788 TCAGCTCACTGTAACCTCCACCACCCAGGTTCAAGGAATTCTCTGCCTCAGCCTCCCGAGTAGCT TCAGCTCACTGTAACCTCCACCACCC_______AGGAATTCTCTGCCTCAGCCTCCCGAGTAGCT CAGGTTCA C VPS45 Ensembl:ENSG00000136631 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1553810611 Functional Loss DEL dbSNP153 27..33 33 - - - 36496 RMVar_ID_36496 Human_SNP_ID_33326759 A-to-I Human chr1 + 150136935 150136935 150136935 TGTTTGTTTGTTTTGAGACAGGGTCTCACCCTATCACCCAGGCTGGAGTGCAGTGGTGCCATCTC TGTTTGTTTGTTTTGAGACAGGGTCTCACCCTGTCACCCAGGCTGGAGTGCAGTGGTGCCATCTC A G VPS45 Ensembl:ENSG00000136631 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1458447922 Functional Loss SNV dbSNP153 33..33 33 - - - 36497 RMVar_ID_36497 Human_SNP_ID_33328027 A-to-I Human chr1 + 150142688 150142687 150142689 CTTGTTGTTGTTGCTGTTGTTGTTGTTGAGACAGGGTTTCACTCCTGTCGCCCAGGTTGGAGTGC CTTGTTGTTGTTGCTGTTGTTGTTGTTGAGAC__GGTTTCACTCCTGTCGCCCAGGTTGGAGTGC CAG C VPS45 Ensembl:ENSG00000136631 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215930969 Functional Loss DEL dbSNP153 33..34 33 - - - 36498 RMVar_ID_36498 Human_SNP_ID_33328058 A-to-I Human chr1 + 150142834 150142834 150142834 CTACAGGCACCTGTCTAATTTTTGTATTTTTTATAGAGATGGGGTTTCACTATGTTCCCCTGCCT CTACAGGCACCTGTCTAATTTTTGTATTTTTTGTAGAGATGGGGTTTCACTATGTTCCCCTGCCT A G VPS45 Ensembl:ENSG00000136631 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs782024926 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_125615,Human_Splice_Rec_125659,Human_Splice_Rec_125831 36499 RMVar_ID_36499 Human_SNP_ID_33328059 A-to-I Human chr1 + 150142838 150142838 150142838 AGGCACCTGTCTAATTTTTGTATTTTTTATAGAGATGGGGTTTCACTATGTTCCCCTGCCTGGTT AGGCACCTGTCTAATTTTTGTATTTTTTATAGGGATGGGGTTTCACTATGTTCCCCTGCCTGGTT A G VPS45 Ensembl:ENSG00000136631 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1553815614 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_125614,Human_Splice_Rec_125615,Human_Splice_Rec_125658,Human_Splice_Rec_125659,Human_Splice_Rec_125830,Human_Splice_Rec_125831 36500 RMVar_ID_36500 Human_SNP_ID_33328076 A-to-I Human chr1 + 150142892 150142892 150142892 CCTGCCTGGTTTCGAACTCCTGGGCTCAAGCGATCCACCCGCCTCAGCCTCCCAAAGTGCTGGGA CCTGCCTGGTTTCGAACTCCTGGGCTCAAGCGGTCCACCCGCCTCAGCCTCCCAAAGTGCTGGGA A G VPS45 Ensembl:ENSG00000136631 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1553815662 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_125614,Human_Splice_Rec_125615,Human_Splice_Rec_125658,Human_Splice_Rec_125659,Human_Splice_Rec_125830,Human_Splice_Rec_125831 36501 RMVar_ID_36501 Human_SNP_ID_33328077 A-to-I Human chr1 + 150142896 150142896 150142896 CCTGGTTTCGAACTCCTGGGCTCAAGCGATCCACCCGCCTCAGCCTCCCAAAGTGCTGGGATTAC CCTGGTTTCGAACTCCTGGGCTCAAGCGATCCCCCCGCCTCAGCCTCCCAAAGTGCTGGGATTAC A C VPS45 Ensembl:ENSG00000136631 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1553815668 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_125614,Human_Splice_Rec_125615,Human_Splice_Rec_125658,Human_Splice_Rec_125659,Human_Splice_Rec_125830,Human_Splice_Rec_125831 36502 RMVar_ID_36502 Human_SNP_ID_33328084 A-to-I Human chr1 + 150142905 150142905 150142905 GAACTCCTGGGCTCAAGCGATCCACCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGCGTAAGC GAACTCCTGGGCTCAAGCGATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGCGTAAGC A G VPS45 Ensembl:ENSG00000136631 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1553815674 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_125614,Human_Splice_Rec_125615,Human_Splice_Rec_125658,Human_Splice_Rec_125659,Human_Splice_Rec_125830,Human_Splice_Rec_125831 36503 RMVar_ID_36503 Human_SNP_ID_33328399 A-to-I Human chr1 + 150144217 150144217 150144217 GCAATCCACCCGCCTCAGCCTTCTAAAGTGCTAGCATTACAGGCCTGAGCCACCGCGCCTGCCTG GCAATCCACCCGCCTCAGCCTTCTAAAGTGCTGGCATTACAGGCCTGAGCCACCGCGCCTGCCTG A G VPS45 Ensembl:ENSG00000136631 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1485664833 Functional Loss SNV dbSNP153 33..33 33 - - - 36504 RMVar_ID_36504 Human_SNP_ID_33339218 A-to-I Human chr1 + 150185367 150185367 150185367 CATGGCGAAACCCCATCTCTACTAAAAATTCAAAAATTAGCCAGGTGTGTTGTTGCGCATCTGTA CATGGCGAAACCCCATCTCTACTAAAAATTCAGAAATTAGCCAGGTGTGTTGTTGCGCATCTGTA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs868976107 Functional Loss SNV dbSNP153 33..33 33 - - - 36505 RMVar_ID_36505 Human_SNP_ID_33349047 A-to-I Human chr1 - 150223927 150223927 150223927 CAGCCTGACCAACATGGAGAAACCCTGTCTCTACTATAAATACAAAATTAGCTGGGCGTGGTGGC CAGCCTGACCAACATGGAGAAACCCTGTCTCTCCTATAAATACAAAATTAGCTGGGCGTGGTGGC T G ANP32E Ensembl:ENSG00000143401 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs971911858 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_368933 36506 RMVar_ID_36506 Human_SNP_ID_33350834 A-to-I Human chr1 - 150231392 150231392 150231392 TAGGGTTTCACCATGTTGTCCAGACTGGTTTCAAATTCCTGGGCTCCGGTCATCCTCCTGCCTCG TAGGGTTTCACCATGTTGTCCAGACTGGTTTCCAATTCCTGGGCTCCGGTCATCCTCCTGCCTCG T G ANP32E Ensembl:ENSG00000143401 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1022368194 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66515,RMVar_hsa_circ_349491,RMVar_hsa_circ_276670 36507 RMVar_ID_36507 Human_SNP_ID_33350842 A-to-I Human chr1 - 150231423 150231423 150231423 ACCTGGCTAATTTTTGTATTTTTTGCAGAGATAGGGTTTCACCATGTTGTCCAGACTGGTTTCAA ACCTGGCTAATTTTTGTATTTTTTGCAGAGATGGGGTTTCACCATGTTGTCCAGACTGGTTTCAA T C ANP32E Ensembl:ENSG00000143401 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1198639980 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66515,RMVar_hsa_circ_349491,RMVar_hsa_circ_276670 36508 RMVar_ID_36508 Human_SNP_ID_33367578 A-to-I Human chr1 + 150294788 150294788 150294788 GGGCGTGGTGGCAAACGCCTGTAATCTCAGCTACTCGAGAGCTGAGGCAGGAGAATCGCTTGAAC GGGCGTGGTGGCAAACGCCTGTAATCTCAGCTGCTCGAGAGCTGAGGCAGGAGAATCGCTTGAAC A G MRPS21 Ensembl:ENSG00000266472 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs889885349 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10567925 36509 RMVar_ID_36509 Human_SNP_ID_33367741 A-to-I Human chr1 + 150295264 150295264 150295264 GTGATCTGCCTGCCTCTGCCTCCCAAAGTGCTAGGATTACAGGCGTAAGCCACAGCGCCCGGCCC GTGATCTGCCTGCCTCTGCCTCCCAAAGTGCTGGGATTACAGGCGTAAGCCACAGCGCCCGGCCC A G MRPS21 Ensembl:ENSG00000266472 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1374741678 Functional Loss SNV dbSNP153 33..33 33 - - - 36510 RMVar_ID_36510 Human_SNP_ID_33368040 A-to-I Human chr1 + 150296228 150296228 150296228 CCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGCATCCGGCCCAGCCCTAGTAGT CCTTGGCCTCCCAAAGTGCTGGGATTACAGGCCTGAGCCACTGCATCCGGCCCAGCCCTAGTAGT A C MRPS21 Ensembl:ENSG00000266472 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025893997 Functional Loss SNV dbSNP153 33..33 33 - - - 36511 RMVar_ID_36511 Human_SNP_ID_33368397 A-to-I Human chr1 + 150297462 150297462 150297462 GGGAGGTTCAGGCGGGTGGATCACCTGAGGTCAGGAGTTCAATACCAGCCTGGCCAACATAGCGA GGGAGGTTCAGGCGGGTGGATCACCTGAGGTCGGGAGTTCAATACCAGCCTGGCCAACATAGCGA A G MRPS21 Ensembl:ENSG00000266472 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1162636773 Functional Loss SNV dbSNP153 33..33 33 - - - 36512 RMVar_ID_36512 Human_SNP_ID_33368802 A-to-I Human chr1 + 150299087 150299087 150299087 AAAATACAAAAATTAGCCATGCATGGTGGCACAGGTCTGTAATCCCAGCTACTCCGTAGGCTGAG AAAATACAAAAATTAGCCATGCATGGTGGCACGGGTCTGTAATCCCAGCTACTCCGTAGGCTGAG A G MRPS21 Ensembl:ENSG00000266472 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1553857115 Functional Loss SNV dbSNP153 33..33 33 - - - 36513 RMVar_ID_36513 Human_SNP_ID_33371528 A-to-I Human chr1 + 150308767 150308767 150308767 CTGAGGCAGGAGAATTGCTTGAACTGGGGAGGAAGAGGTTGCAGTGAGCCAAGATCATGCCACTG CTGAGGCAGGAGAATTGCTTGAACTGGGGAGGCAGAGGTTGCAGTGAGCCAAGATCATGCCACTG A C MRPS21 Ensembl:ENSG00000266472 Protein coding 3'UTR GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs580060 Functional Loss SNV dbSNP153 33..33 33 - - - 36514 RMVar_ID_36514 Human_SNP_ID_33371631 A-to-I Human chr1 + 150309096 150309096 150309096 TAGGCTCACTGCAACCTCCGCCTCCTGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCCAGAAGC TAGGCTCACTGCAACCTCCGCCTCCTGGGTTCGAGTGATTCTCCTGCCTCAGCCTCCCCAGAAGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1192264657 Functional Loss SNV dbSNP153 33..33 33 - - - 36515 RMVar_ID_36515 Human_SNP_ID_33371745 A-to-I Human chr1 + 150309365 150309365 150309365 GCTCTGTTGCCCAGGCTGGAGGGCAGTGGGACAATCTCAGCTCACTGCAAGCTCCGCCGCCTGGG GCTCTGTTGCCCAGGCTGGAGGGCAGTGGGACCATCTCAGCTCACTGCAAGCTCCGCCGCCTGGG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202626006 Functional Loss SNV dbSNP153 33..33 33 - - - 36516 RMVar_ID_36516 Human_SNP_ID_33371746 A-to-I Human chr1 + 150309365 150309365 150309365 GCTCTGTTGCCCAGGCTGGAGGGCAGTGGGACAATCTCAGCTCACTGCAAGCTCCGCCGCCTGGG GCTCTGTTGCCCAGGCTGGAGGGCAGTGGGACGATCTCAGCTCACTGCAAGCTCCGCCGCCTGGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202626006 Functional Loss SNV dbSNP153 33..33 33 - - - 36517 RMVar_ID_36517 Human_SNP_ID_33377033 A-to-I Human chr1 + 150329853 150329853 150329853 GCGATCTCGGTTCACTGCAGCCTCTGCCTCCCAGGTTCAAGTGATTCTCCTGCCTCAGCCTCCTA GCGATCTCGGTTCACTGCAGCCTCTGCCTCCCGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCTA A G PRPF3 Ensembl:ENSG00000117360 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1375018837 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6841,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_60201 36518 RMVar_ID_36518 Human_SNP_ID_33378500 A-to-I Human chr1 + 150335650 150335650 150335650 ACCACGCCTGGCTAATTTTGTATTTTTGGTGGAGACGGGGTTTCTCCGTGTTGGTCAGGCTGGTC ACCACGCCTGGCTAATTTTGTATTTTTGGTGGGGACGGGGTTTCTCCGTGTTGGTCAGGCTGGTC A G PRPF3 Ensembl:ENSG00000117360 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1286733979 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_310454,RMVar_hsa_circ_19437,RMVar_hsa_circ_352571,RMVar_hsa_circ_362153,RMVar_hsa_circ_60201,RMVar_hsa_circ_293437,RMVar_hsa_circ_354461,RMVar_hsa_circ_368495,RMVar_hsa_circ_324343 36519 RMVar_ID_36519 Human_SNP_ID_33379522 A-to-I Human chr1 + 150339157 150339157 150339157 GGAGGCTGAGGGCTGAAGGATTGCTTGAGCCCAGGAGTTAAAGACCAGCTTGGGCAATATGGTGA GGAGGCTGAGGGCTGAAGGATTGCTTGAGCCCGGGAGTTAAAGACCAGCTTGGGCAATATGGTGA A G PRPF3 Ensembl:ENSG00000117360 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1432556051 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_310454,RMVar_hsa_circ_19437,RMVar_hsa_circ_352571,RMVar_hsa_circ_60201,RMVar_hsa_circ_354461,RMVar_hsa_circ_324343,RMVar_hsa_circ_60325,RMVar_hsa_circ_311140 36520 RMVar_ID_36520 Human_SNP_ID_33379751 A-to-I Human chr1 + 150339803 150339803 150339803 TCTCACTCTGTTGCACAATCTCGGCTCGCTGCAACCTCTGTCTCCTGGGTTGAAGCAGTTCTTCT TCTCACTCTGTTGCACAATCTCGGCTCGCTGCCACCTCTGTCTCCTGGGTTGAAGCAGTTCTTCT A C PRPF3 Ensembl:ENSG00000117360 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs587646656 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_310454,RMVar_hsa_circ_19437,RMVar_hsa_circ_352571,RMVar_hsa_circ_60201,RMVar_hsa_circ_354461,RMVar_hsa_circ_324343,RMVar_hsa_circ_60325,RMVar_hsa_circ_311140 36521 RMVar_ID_36521 Human_SNP_ID_33379947 A-to-I Human chr1 + 150340751 150340751 150340751 CCTCTAATCCAAACACTTTCGGAGGCCAAGGCAGGAGGATTGCTTGAGGCCAAGAATTCAAGACC CCTCTAATCCAAACACTTTCGGAGGCCAAGGCGGGAGGATTGCTTGAGGCCAAGAATTCAAGACC A G PRPF3 Ensembl:ENSG00000117360 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs758675895 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88682,RMVar_hsa_circ_19437,RMVar_hsa_circ_60201,RMVar_hsa_circ_60325,RMVar_hsa_circ_329976,RMVar_hsa_circ_27171,RMVar_hsa_circ_135877 36522 RMVar_ID_36522 Human_SNP_ID_33380310 A-to-I Human chr1 + 150341861 150341861 150341861 GAGTAGCTTGGATTATAGGTGCCTGCCACCACACCTGGCTAGTTTTTGAACTTTTAGTAGAGACA GAGTAGCTTGGATTATAGGTGCCTGCCACCACCCCTGGCTAGTTTTTGAACTTTTAGTAGAGACA A C PRPF3 Ensembl:ENSG00000117360 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs920469570 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10568942 RMVar_hsa_circ_88682,RMVar_hsa_circ_19437,RMVar_hsa_circ_60201,RMVar_hsa_circ_60325,RMVar_hsa_circ_329976,RMVar_hsa_circ_27171,RMVar_hsa_circ_135877 36523 RMVar_ID_36523 Human_SNP_ID_33380329 A-to-I Human chr1 + 150341951 150341951 150341951 GTCTTGAACTCCTGACCTCAAGTGATCTGCCCACCTAGGCTTCCCAAAGTGCTGGGTTTACCGGC GTCTTGAACTCCTGACCTCAAGTGATCTGCCCGCCTAGGCTTCCCAAAGTGCTGGGTTTACCGGC A G PRPF3 Ensembl:ENSG00000117360 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1211070504 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88682,RMVar_hsa_circ_19437,RMVar_hsa_circ_60201,RMVar_hsa_circ_60325,RMVar_hsa_circ_329976,RMVar_hsa_circ_27171,RMVar_hsa_circ_135877 36524 RMVar_ID_36524 Human_SNP_ID_33381627 A-to-I Human chr1 + 150346980 150346980 150346980 GGATGTGGTGGCACACACCTGTATTCCCAGCTACTCAGGAAGCTGAGGTGGGAGGATCACTTGAG GGATGTGGTGGCACACACCTGTATTCCCAGCTTCTCAGGAAGCTGAGGTGGGAGGATCACTTGAG A T PRPF3 Ensembl:ENSG00000117360 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1357647470 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60325,RMVar_hsa_circ_59451 36525 RMVar_ID_36525 Human_SNP_ID_33381832 A-to-I Human chr1 + 150347506 150347506 150347506 TAATCTGAGCACTTTGGGAGGCCGAGGCGAGCAGATCATTTGAGGTCAGGAGTTCGTAACAGCCT TAATCTGAGCACTTTGGGAGGCCGAGGCGAGCGGATCATTTGAGGTCAGGAGTTCGTAACAGCCT A G PRPF3 Ensembl:ENSG00000117360 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1136373 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10569122 RMVar_hsa_circ_60325,RMVar_hsa_circ_59451 36526 RMVar_ID_36526 Human_SNP_ID_33381852 A-to-I Human chr1 + 150347565 150347565 150347565 CAGCCTGGCCAACATGGTGAAACCCCGTCTCTACTGAAAACACAAAAATTCGGGGCGTGGTGGTG CAGCCTGGCCAACATGGTGAAACCCCGTCTCTCCTGAAAACACAAAAATTCGGGGCGTGGTGGTG A C PRPF3 Ensembl:ENSG00000117360 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1317351674 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60325,RMVar_hsa_circ_59451 36527 RMVar_ID_36527 Human_SNP_ID_33382657 A-to-I Human chr1 + 150350381 150350381 150350381 GAGCCACCACGCCTGGCTAATTTTGTATTTTTAGTAGAGACGGGGTTTCGCCATATTGGTCAAGC GAGCCACCACGCCTGGCTAATTTTGTATTTTTGGTAGAGACGGGGTTTCGCCATATTGGTCAAGC A G PRPF3 Ensembl:ENSG00000117360 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1238370718 Functional Loss SNV dbSNP153 33..33 33 - - - 36528 RMVar_ID_36528 Human_SNP_ID_33382663 A-to-I Human chr1 + 150350403 150350403 150350403 TTGTATTTTTAGTAGAGACGGGGTTTCGCCATATTGGTCAAGCTGGTCTCGAACTCCTGACCTGA TTGTATTTTTAGTAGAGACGGGGTTTCGCCATGTTGGTCAAGCTGGTCTCGAACTCCTGACCTGA A G PRPF3 Ensembl:ENSG00000117360 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs911029814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24584204 36529 RMVar_ID_36529 Human_SNP_ID_33382726 A-to-I Human chr1 + 150350703 150350703 150350703 CTTACTGAGACCCAGCACAGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGATGAGGTGGTT CTTACTGAGACCCAGCACAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGATGAGGTGGTT A G PRPF3 Ensembl:ENSG00000117360 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1035742505 Functional Loss SNV dbSNP153 33..33 33 - - - 36530 RMVar_ID_36530 Human_SNP_ID_33382998 A-to-I Human chr1 + 150351784 150351784 150351784 CTCCCACCTCAGCCTCCCAAAGTGCTGGGATTATAGGCATGAGCTACTGTGCCCAGCCCTACCTT CTCCCACCTCAGCCTCCCAAAGTGCTGGGATTGTAGGCATGAGCTACTGTGCCCAGCCCTACCTT A G PRPF3 Ensembl:ENSG00000117360 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1435358604 Functional Loss SNV dbSNP153 33..33 33 - - - 36531 RMVar_ID_36531 Human_SNP_ID_33382999 A-to-I Human chr1 + 150351790 150351790 150351790 CCTCAGCCTCCCAAAGTGCTGGGATTATAGGCATGAGCTACTGTGCCCAGCCCTACCTTCACATA CCTCAGCCTCCCAAAGTGCTGGGATTATAGGCGTGAGCTACTGTGCCCAGCCCTACCTTCACATA A G PRPF3 Ensembl:ENSG00000117360 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs942879721 Functional Loss SNV dbSNP153 33..33 33 - - - 36532 RMVar_ID_36532 Human_SNP_ID_33389891 A-to-I Human chr1 + 150377117 150377117 150377117 CCTGTAGTCTCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCTTGAACCCAGGAGGCAGCAGTT CCTGTAGTCTCAGCTACTCGGGAGGCTGAGGCGGGAGAATTGCTTGAACCCAGGAGGCAGCAGTT A G RPRD2 Ensembl:ENSG00000163125 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1257819549 Functional Loss SNV dbSNP153 33..33 33 - - - 36533 RMVar_ID_36533 Human_SNP_ID_33390816 A-to-I Human chr1 + 150380477 150380477 150380477 GCAAGCAGTTCTCCTGTCTCAGCCTCTGAAGTAGCTGGGATTATAGGCATACACCACCATGCCCA GCAAGCAGTTCTCCTGTCTCAGCCTCTGAAGTCGCTGGGATTATAGGCATACACCACCATGCCCA A C RPRD2 Ensembl:ENSG00000163125 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1246426781 Functional Loss SNV dbSNP153 33..33 33 - - - 36534 RMVar_ID_36534 Human_SNP_ID_33392925 A-to-I Human chr1 + 150387986 150387986 150387986 TCACCCAGGCTGGAGTGCAGTGGTGTGATCTCAGCTCAATGTAACCTCTGCCTCCTAGACTTCAG TCACCCAGGCTGGAGTGCAGTGGTGTGATCTCGGCTCAATGTAACCTCTGCCTCCTAGACTTCAG A G RPRD2 Ensembl:ENSG00000163125 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1553882284 Functional Loss SNV dbSNP153 33..33 33 - - - 36535 RMVar_ID_36535 Human_SNP_ID_33396521 A-to-I Human chr1 + 150401326 150401326 150401326 CCTGGCCAACATGGTGAAACCCTGTCTCTCCTAAACATACAAAAATTAGCTGGGTATGGTGGTGC CCTGGCCAACATGGTGAAACCCTGTCTCTCCTGAACATACAAAAATTAGCTGGGTATGGTGGTGC A G RPRD2 Ensembl:ENSG00000163125 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1403071701 Functional Loss SNV dbSNP153 33..33 33 - - - 36536 RMVar_ID_36536 Human_SNP_ID_33396532 A-to-I Human chr1 + 150401367 150401367 150401367 AAAATTAGCTGGGTATGGTGGTGCAAGCCTGTAGTTACAGCTACTCGGGACGCCAAGGCAGAAGA AAAATTAGCTGGGTATGGTGGTGCAAGCCTGTGGTTACAGCTACTCGGGACGCCAAGGCAGAAGA A G RPRD2 Ensembl:ENSG00000163125 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs587613390 Functional Loss SNV dbSNP153 33..33 33 - - - 36537 RMVar_ID_36537 Human_SNP_ID_33396541 A-to-I Human chr1 + 150401389 150401389 150401389 GCAAGCCTGTAGTTACAGCTACTCGGGACGCCAAGGCAGAAGAATTGCTTGAACCTGTGAGACGG GCAAGCCTGTAGTTACAGCTACTCGGGACGCCGAGGCAGAAGAATTGCTTGAACCTGTGAGACGG A G RPRD2 Ensembl:ENSG00000163125 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1303386909 Functional Loss SNV dbSNP153 33..33 33 - - - 36538 RMVar_ID_36538 Human_SNP_ID_33405052 A-to-I Human chr1 + 150434566 150434566 150434566 GGCTGGGCCCTGTGGCTTACACCTGTAATCCCAACACTTTGGGAGGCCGAGGCGGGTGGATCATT GGCTGGGCCCTGTGGCTTACACCTGTAATCCCCACACTTTGGGAGGCCGAGGCGGGTGGATCATT A C RPRD2 Ensembl:ENSG00000163125 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1401284187 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9881,RMVar_hsa_circ_354670,RMVar_hsa_circ_312122,RMVar_hsa_circ_60908,RMVar_hsa_circ_135883,RMVar_hsa_circ_351175,RMVar_hsa_circ_135881,RMVar_hsa_circ_341797,RMVar_hsa_circ_270473 36539 RMVar_ID_36539 Human_SNP_ID_33410089 A-to-I Human chr1 + 150454701 150454701 150454701 GAAATTTTGTCTCAACAAAAAATACAAAAATTAGCCAGGAGTGGTGGTATGTGCCTGTAGTCCCA GAAATTTTGTCTCAACAAAAAATACAAAAATTGGCCAGGAGTGGTGGTATGTGCCTGTAGTCCCA A G RPRD2 Ensembl:ENSG00000163125 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1216196089 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_354670,RMVar_hsa_circ_60908,RMVar_hsa_circ_135884,RMVar_hsa_circ_351175,RMVar_hsa_circ_342773,RMVar_hsa_circ_367888,RMVar_hsa_circ_52370,RMVar_hsa_circ_135891,RMVar_hsa_circ_135889,RMVar_hsa_circ_68120,RMVar_hsa_circ_330137,RMVar_hsa_circ_329734,RMVar_hsa_circ_135893,RMVar_hsa_circ_297419,RMVar_hsa_circ_135892,RMVar_hsa_circ_330648,RMVar_hsa_circ_360845,RMVar_hsa_circ_300434,RMVar_hsa_circ_135895,RMVar_hsa_circ_135896 36540 RMVar_ID_36540 Human_SNP_ID_33411038 A-to-I Human chr1 + 150458740 150458740 150458740 TGGCTCACTGCATCCTCCATCTCCTGCGTTCAAACAATTCTCCTGCCTCAGCCTCCCGAGTAGCT TGGCTCACTGCATCCTCCATCTCCTGCGTTCAGACAATTCTCCTGCCTCAGCCTCCCGAGTAGCT A G RPRD2 Ensembl:ENSG00000163125 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs868933656 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60908,RMVar_hsa_circ_40614,RMVar_hsa_circ_342773,RMVar_hsa_circ_52370,RMVar_hsa_circ_135889,RMVar_hsa_circ_68120,RMVar_hsa_circ_330137,RMVar_hsa_circ_329734,RMVar_hsa_circ_135893,RMVar_hsa_circ_135892,RMVar_hsa_circ_360845,RMVar_hsa_circ_300434,RMVar_hsa_circ_135896,RMVar_hsa_circ_332855,RMVar_hsa_circ_135898 36541 RMVar_ID_36541 Human_SNP_ID_33413317 A-to-I Human chr1 + 150467648 150467648 150467648 CACCTGCCTCGACCTCCCAAAGTGCTGGGATTACAGGTGTGAACCACCGTGCCTGGCCGATGTGA CACCTGCCTCGACCTCCCAAAGTGCTGGGATTGCAGGTGTGAACCACCGTGCCTGGCCGATGTGA A G RPRD2 Ensembl:ENSG00000163125 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041547176 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_135899,RMVar_hsa_circ_109119 36542 RMVar_ID_36542 Human_SNP_ID_33413405 A-to-I Human chr1 + 150468051 150468051 150468051 GGGCGTGGTGGCTCACAGCTGTAACCCCAACTACTTGGGAGGCTGAGGTAGGAGAATCGCTTGAA GGGCGTGGTGGCTCACAGCTGTAACCCCAACTGCTTGGGAGGCTGAGGTAGGAGAATCGCTTGAA A G RPRD2 Ensembl:ENSG00000163125 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs994171904 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_135899,RMVar_hsa_circ_109119 36543 RMVar_ID_36543 Human_SNP_ID_33413446 A-to-I Human chr1 + 150468240 150468240 150468240 GGCTGGGCGCAGTGGCTCATGCCTGTAATCCTAACACTTTGGGAGGCCACGATGGGAGGATCACT GGCTGGGCGCAGTGGCTCATGCCTGTAATCCTGACACTTTGGGAGGCCACGATGGGAGGATCACT A G RPRD2 Ensembl:ENSG00000163125 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs939722414 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_135899,RMVar_hsa_circ_109119 36544 RMVar_ID_36544 Human_SNP_ID_33419806 A-to-I Human chr1 + 150492065 150492065 150492065 CTCGGCTCACTGCATCTCTGCCTCCCGGGTTCAAACAATTCTTCTGCCTCAGCCTCCCGAGTAGC CTCGGCTCACTGCATCTCTGCCTCCCGGGTTCGAACAATTCTTCTGCCTCAGCCTCCCGAGTAGC A G TARS2 Ensembl:ENSG00000143374 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs756804058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10571236 RMVar_hsa_circ_94626,RMVar_hsa_circ_135901,RMVar_hsa_circ_135902,RMVar_hsa_circ_135903,RMVar_hsa_circ_74007,RMVar_hsa_circ_307289,RMVar_hsa_circ_318847,RMVar_hsa_circ_352559,RMVar_hsa_circ_135904,RMVar_hsa_circ_372302 36545 RMVar_ID_36545 Human_SNP_ID_33419807 A-to-I Human chr1 + 150492065 150492065 150492065 CTCGGCTCACTGCATCTCTGCCTCCCGGGTTCAAACAATTCTTCTGCCTCAGCCTCCCGAGTAGC CTCGGCTCACTGCATCTCTGCCTCCCGGGTTCTAACAATTCTTCTGCCTCAGCCTCCCGAGTAGC A T TARS2 Ensembl:ENSG00000143374 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs756804058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10571236 RMVar_hsa_circ_94626,RMVar_hsa_circ_135901,RMVar_hsa_circ_135902,RMVar_hsa_circ_135903,RMVar_hsa_circ_74007,RMVar_hsa_circ_307289,RMVar_hsa_circ_318847,RMVar_hsa_circ_352559,RMVar_hsa_circ_135904,RMVar_hsa_circ_372302 36546 RMVar_ID_36546 Human_SNP_ID_33420322 A-to-I Human chr1 + 150493899 150493899 150493899 TGAACTTAGACTGGGCATGGTGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCCAAGGTGGGT TGAACTTAGACTGGGCATGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGT A G TARS2 Ensembl:ENSG00000143374 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs899410787 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94626,RMVar_hsa_circ_135902,RMVar_hsa_circ_74007,RMVar_hsa_circ_318847,RMVar_hsa_circ_271608,RMVar_hsa_circ_341937,RMVar_hsa_circ_309210,RMVar_hsa_circ_270719,RMVar_hsa_circ_135906,RMVar_hsa_circ_135908,RMVar_hsa_circ_100183,RMVar_hsa_circ_135907 36547 RMVar_ID_36547 Human_SNP_ID_33420499 A-to-I Human chr1 + 150494478 150494478 150494478 ATACAGACTGTCGGCCAGGTGCGGTGGTTCACACGTGTAATCCCAACACTTTGGGAGGCCAAGTT ATACAGACTGTCGGCCAGGTGCGGTGGTTCACCCGTGTAATCCCAACACTTTGGGAGGCCAAGTT A C TARS2 Ensembl:ENSG00000143374 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1349033992 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94626,RMVar_hsa_circ_135902,RMVar_hsa_circ_74007,RMVar_hsa_circ_318847,RMVar_hsa_circ_271608,RMVar_hsa_circ_341937,RMVar_hsa_circ_309210,RMVar_hsa_circ_270719,RMVar_hsa_circ_135906,RMVar_hsa_circ_135908,RMVar_hsa_circ_100183,RMVar_hsa_circ_135907 36548 RMVar_ID_36548 Human_SNP_ID_33420585 A-to-I Human chr1 + 150494774 150494774 150494774 AATATACATATAGGGGCTGGGCGTGGTGGCTCACGCCTGTAATCCTAACACTTTGGGAGGCTGAG AATATACATATAGGGGCTGGGCGTGGTGGCTCCCGCCTGTAATCCTAACACTTTGGGAGGCTGAG A C TARS2 Ensembl:ENSG00000143374 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1441987383 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94626,RMVar_hsa_circ_135902,RMVar_hsa_circ_74007,RMVar_hsa_circ_318847,RMVar_hsa_circ_271608,RMVar_hsa_circ_341937,RMVar_hsa_circ_309210,RMVar_hsa_circ_270719,RMVar_hsa_circ_135906,RMVar_hsa_circ_135908,RMVar_hsa_circ_100183,RMVar_hsa_circ_135907 36549 RMVar_ID_36549 Human_SNP_ID_33422178 A-to-I Human chr1 + 150500425 150500425 150500425 CAGCCTGGCCAACGTGGCGAAACCCCATCTCTACTAAAAATATAAAAATTGGCCGGGTGAGGTGT CAGCCTGGCCAACGTGGCGAAACCCCATCTCTGCTAAAAATATAAAAATTGGCCGGGTGAGGTGT A G TARS2 Ensembl:ENSG00000143374 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1439708442 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79295,RMVar_hsa_circ_135908,RMVar_hsa_circ_100183,RMVar_hsa_circ_135910 36550 RMVar_ID_36550 Human_SNP_ID_33423455 A-to-I Human chr1 - 150504572 150504572 150504572 GGAATGGTGGAAGTATCACGAATTGTGTACCCAAGATCACCTTCCAGTTTTTAAGAAATATTCAG GGAATGGTGGAAGTATCACGAATTGTGTACCCGAGATCACCTTCCAGTTTTTAAGAAATATTCAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs587626507 Functional Loss SNV dbSNP153 33..33 33 - - - 36551 RMVar_ID_36551 Human_SNP_ID_33427454 A-to-I Human chr1 + 150518602 150518602 150518602 GAGACATGGGGTTTCTCCATGTCGTTCAGGCTAGTCCCGAACTCCTGACCTCAGGTGATCCGCCT GAGACATGGGGTTTCTCCATGTCGTTCAGGCTGGTCCCGAACTCCTGACCTCAGGTGATCCGCCT A G FALEC RNACentral:URS00008C10F0 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1442895988 Functional Loss SNV dbSNP153 33..33 33 - - - 36552 RMVar_ID_36552 Human_SNP_ID_33441149 A-to-I Human chr1 - 150565726 150565726 150565726 AGGCGGGAGGATTGCTTGAGCTTAGGAGTTCAAGTCTAGCCTAGGCAACATAGTGAGACCCTGTC AGGCGGGAGGATTGCTTGAGCTTAGGAGTTCAGGTCTAGCCTAGGCAACATAGTGAGACCCTGTC T C ADAMTSL4-AS1 Ensembl:ENSG00000203804 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1000076734 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1149433 36553 RMVar_ID_36553 Human_SNP_ID_33445376 A-to-I Human chr1 - 150579318 150579318 150579318 GCCGGCGCAAGCCCCCCGTCCACCCTCACGCCAGACTCCCGGAGGGTCGCGCGGCCGCCGCCCAT GCCGGCGCAAGCCCCCCGTCCACCCTCACGCCGGACTCCCGGAGGGTCGCGCGGCCGCCGCCCAT T C MCL1 Ensembl:ENSG00000143384 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1229212054 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3992093,Human_RBP_ID_9319128,Human_RBP_ID_17762860,Human_RBP_ID_22023791,Human_RBP_ID_22428571,Human_RBP_ID_22532148,Human_RBP_ID_26753427 RMVar_hsa_circ_75621,RMVar_hsa_circ_135920 36554 RMVar_ID_36554 Human_SNP_ID_33446204 A-to-I Human chr1 - 150581676 150581664 150581676 TCTGTAATCCCAACACTTTGGGAGGCCAAGGTAGGAGGATCACCTGAGTCCAGGAGTTCAAGACC TCTGTAATCCCAACACTTTGGGAGGCCAAGGT____________TGAGTCCAGGAGTTCAAGACC AGGTGATCCTCCT A RF00017-1784 RNACentral:URS0000904F64 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1196163424 Functional Loss DEL dbSNP153 33..44 33 - - - 36555 RMVar_ID_36555 Human_SNP_ID_33448858 A-to-I Human chr1 - 150591573 150591573 150591573 TGGCCAATATGGTGAAACCCCGTGTCCACCAAAAATACAAAAATTAGCCGGGCGTGGTAGCACGT TGGCCAATATGGTGAAACCCCGTGTCCACCAAGAATACAAAAATTAGCCGGGCGTGGTAGCACGT T C RF00017-1784 RNACentral:URS0000904F64 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs587774217 Functional Loss SNV dbSNP153 33..33 33 - - - 36556 RMVar_ID_36556 Human_SNP_ID_33450488 A-to-I Human chr1 - 150597524 150597524 150597524 TGAGGCCAGGAGTTTTAAGGCTGTAGTGTGCTATGAATGCACCTGTGAATAGCAGCTGTGCTCCA TGAGGCCAGGAGTTTTAAGGCTGTAGTGTGCTGTGAATGCACCTGTGAATAGCAGCTGTGCTCCA T C RF00017-1784 RNACentral:URS0000904F64 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs988116894 Functional Loss SNV dbSNP153 33..33 33 - - - 36557 RMVar_ID_36557 Human_SNP_ID_33450496 A-to-I Human chr1 - 150597567 150597567 150597567 CTATAGTCCCAGCTACTTCAGAGGCTAACGTTAGAGGATCATCTGAGGCCAGGAGTTTTAAGGCT CTATAGTCCCAGCTACTTCAGAGGCTAACGTTCGAGGATCATCTGAGGCCAGGAGTTTTAAGGCT T G RF00017-1784 RNACentral:URS0000904F64 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs892771668 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10572076 36558 RMVar_ID_36558 Human_SNP_ID_33450508 A-to-I Human chr1 - 150597617 150597617 150597617 TGCATTTGACCCATTTAAACTGCATCTTAGCTAGGTGCAGTGGGGTATGCCTATAGTCCCAGCTA TGCATTTGACCCATTTAAACTGCATCTTAGCTGGGTGCAGTGGGGTATGCCTATAGTCCCAGCTA T C RF00017-1784 RNACentral:URS0000904F64 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1188818726 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5687446 36559 RMVar_ID_36559 Human_SNP_ID_33450691 A-to-I Human chr1 - 150598268 150598268 150598268 GAGATCATAGCTCACTGTAGCCTTGAACTCCTAGGCTCAAAAGATCCTCCCATCTTAGTTTCTCT GAGATCATAGCTCACTGTAGCCTTGAACTCCTGGGCTCAAAAGATCCTCCCATCTTAGTTTCTCT T C RF00017-1784 RNACentral:URS0000904F64 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1135975 Functional Loss SNV dbSNP153 33..33 33 - - - 36560 RMVar_ID_36560 Human_SNP_ID_33451181 A-to-I Human chr1 - 150600247 150600247 150600247 AGGAGTTGGAGGCTGCACTGAGCTTTGATGGCACCACTCTACTCCAGCCTTCGTAACAAAGACCT AGGAGTTGGAGGCTGCACTGAGCTTTGATGGCGCCACTCTACTCCAGCCTTCGTAACAAAGACCT T C RF00017-1784 RNACentral:URS0000904F64 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1003674098 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5687456 36561 RMVar_ID_36561 Human_SNP_ID_33451259 A-to-I Human chr1 - 150600696 150600696 150600696 ACGGGGTTTCACCATATTGGTCAGGCTGTCTCAAATTCCTGACCTCGTGCTCTGCCCTCCTCGGC ACGGGGTTTCACCATATTGGTCAGGCTGTCTCTAATTCCTGACCTCGTGCTCTGCCCTCCTCGGC T A RF00017-1784 RNACentral:URS0000904F64 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1476426937 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21998260,Human_RBP_ID_24584918 36562 RMVar_ID_36562 Human_SNP_ID_33451295 A-to-I Human chr1 - 150600839 150600839 150600839 AATGCAACCTCCGCCTCCCGGATTCTGGCTCAATGCAACCTCTGCCTCCCGGATTCAAGCGATTC AATGCAACCTCCGCCTCCCGGATTCTGGCTCAGTGCAACCTCTGCCTCCCGGATTCAAGCGATTC T C RF00017-1784 RNACentral:URS0000904F64 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs771215066 Functional Loss SNV dbSNP153 33..33 33 - - - 36563 RMVar_ID_36563 Human_SNP_ID_33451617 A-to-I Human chr1 - 150602052 150602052 150602052 TTGCCCAGGCTGATCTTGAATTCCTGGACTCAAGCGATCTGCCTGCCTTGGCCTCCCAAAATGCT TTGCCCAGGCTGATCTTGAATTCCTGGACTCAGGCGATCTGCCTGCCTTGGCCTCCCAAAATGCT T C ENSA Ensembl:ENSG00000143420 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1370233477 Functional Loss SNV dbSNP153 33..33 33 - - - 36564 RMVar_ID_36564 Human_SNP_ID_33451642 A-to-I Human chr1 - 150602177 150602177 150602177 ACCCTCTGCCTCCCAGACCAAGTAATCCTCCCACTTTGGCCTCCAGAGTAGCTGGGACTACAGGC ACCCTCTGCCTCCCAGACCAAGTAATCCTCCCCCTTTGGCCTCCAGAGTAGCTGGGACTACAGGC T G ENSA Ensembl:ENSG00000143420 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1260198555 Functional Loss SNV dbSNP153 33..33 33 - - - 36565 RMVar_ID_36565 Human_SNP_ID_33452574 A-to-I Human chr1 - 150605818 150605818 150605818 CCTGGCCAAATGGTGAAACCCCGTTTTTACTAAAAATACAAAAATTAGCAGGGTGTGGTGGTGGG CCTGGCCAAATGGTGAAACCCCGTTTTTACTAGAAATACAAAAATTAGCAGGGTGTGGTGGTGGG T C ENSA Ensembl:ENSG00000143420 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1050728972 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22846641 36566 RMVar_ID_36566 Human_SNP_ID_33452861 A-to-I Human chr1 - 150607057 150607057 150607057 CGCAACCACACCTGGCTTATTTTTGTATTTTTAGTAGAGATGGAGTTTCACCATGTTGGCCAAGC CGCAACCACACCTGGCTTATTTTTGTATTTTTGGTAGAGATGGAGTTTCACCATGTTGGCCAAGC T C ENSA Ensembl:ENSG00000143420 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs868102829 Functional Loss SNV dbSNP153 33..33 33 - - - 36567 RMVar_ID_36567 Human_SNP_ID_33452862 A-to-I Human chr1 - 150607057 150607057 150607057 CGCAACCACACCTGGCTTATTTTTGTATTTTTAGTAGAGATGGAGTTTCACCATGTTGGCCAAGC CGCAACCACACCTGGCTTATTTTTGTATTTTTCGTAGAGATGGAGTTTCACCATGTTGGCCAAGC T G ENSA Ensembl:ENSG00000143420 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs868102829 Functional Loss SNV dbSNP153 33..33 33 - - - 36568 RMVar_ID_36568 Human_SNP_ID_33452868 A-to-I Human chr1 - 150607098 150607098 150607098 ATTCTACCTCAGCCTCCCAAGTAGCTGGGATTATGGGCACCCGCAACCACACCTGGCTTATTTTT ATTCTACCTCAGCCTCCCAAGTAGCTGGGATTGTGGGCACCCGCAACCACACCTGGCTTATTTTT T C ENSA Ensembl:ENSG00000143420 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs889691061 Functional Loss SNV dbSNP153 33..33 33 - - - 36569 RMVar_ID_36569 Human_SNP_ID_33452877 A-to-I Human chr1 - 150607159 150607159 150607159 AGAGTGCAGTAGTGCAATCTCGGTTCAGTGCAACCTCCACCTCCCGGGTTCAAACAGTTCTATTC AGAGTGCAGTAGTGCAATCTCGGTTCAGTGCAGCCTCCACCTCCCGGGTTCAAACAGTTCTATTC T C ENSA Ensembl:ENSG00000143420 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs998040296 Functional Loss SNV dbSNP153 33..33 33 - - - 36570 RMVar_ID_36570 Human_SNP_ID_33452929 A-to-I Human chr1 - 150607366 150607366 150607366 GGGAGGCTGAGGTAGGAGAATTGCTTGAACCCAGGAGGCAGGAGGTTGCAGTGAGCTGAGATTGT GGGAGGCTGAGGTAGGAGAATTGCTTGAACCCTGGAGGCAGGAGGTTGCAGTGAGCTGAGATTGT T A ENSA Ensembl:ENSG00000143420 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1426315338 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24584972 36571 RMVar_ID_36571 Human_SNP_ID_33452940 A-to-I Human chr1 - 150607411 150607411 150607411 CAAAAATTAGCTGGTGGTGACGCACACCTGTAATCCCAGCTACTCGGGAGGCTGAGGTAGGAGAA CAAAAATTAGCTGGTGGTGACGCACACCTGTAGTCCCAGCTACTCGGGAGGCTGAGGTAGGAGAA T C ENSA Ensembl:ENSG00000143420 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs943903647 Functional Loss SNV dbSNP153 33..33 33 - - - 36572 RMVar_ID_36572 Human_SNP_ID_33453785 A-to-I Human chr1 - 150610912 150610912 150610912 GGCTGGGCTGGGCGTGGTGCCTTATGCCCACAATCCCAGCATTTTGGGAGGCCAAGATGGGAGGA GGCTGGGCTGGGCGTGGTGCCTTATGCCCACAGTCCCAGCATTTTGGGAGGCCAAGATGGGAGGA T C ENSA Ensembl:ENSG00000143420 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1008975932 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5687505 36573 RMVar_ID_36573 Human_SNP_ID_33454309 A-to-I Human chr1 - 150613116 150613116 150613116 GCCATCACACCCAGCTAATTTTTTGTATTTTTAGTAGAGATGGGGTTTCATCATGTTGGCCAGGC GCCATCACACCCAGCTAATTTTTTGTATTTTTGGTAGAGATGGGGTTTCATCATGTTGGCCAGGC T C ENSA Ensembl:ENSG00000143420 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947247480 Functional Loss SNV dbSNP153 33..33 33 - - - 36574 RMVar_ID_36574 Human_SNP_ID_33454316 A-to-I Human chr1 - 150613140 150613140 150613140 TCTCCTGCCGCAGCCTCCCAGGTAGCCATCACACCCAGCTAATTTTTTGTATTTTTAGTAGAGAT TCTCCTGCCGCAGCCTCCCAGGTAGCCATCACGCCCAGCTAATTTTTTGTATTTTTAGTAGAGAT T C ENSA Ensembl:ENSG00000143420 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985310006 Functional Loss SNV dbSNP153 33..33 33 - - - 36575 RMVar_ID_36575 Human_SNP_ID_33454322 A-to-I Human chr1 - 150613174 150613174 150613174 TCACTGCAACCTCCACCTCCTAGATTCAAGCGATTCTCCTGCCGCAGCCTCCCAGGTAGCCATCA TCACTGCAACCTCCACCTCCTAGATTCAAGCGCTTCTCCTGCCGCAGCCTCCCAGGTAGCCATCA T G ENSA Ensembl:ENSG00000143420 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1434145490 Functional Loss SNV dbSNP153 33..33 33 - - - 36576 RMVar_ID_36576 Human_SNP_ID_33454327 A-to-I Human chr1 - 150613185 150613185 150613185 GCAATCTCGGCTCACTGCAACCTCCACCTCCTAGATTCAAGCGATTCTCCTGCCGCAGCCTCCCA GCAATCTCGGCTCACTGCAACCTCCACCTCCTCGATTCAAGCGATTCTCCTGCCGCAGCCTCCCA T G ENSA Ensembl:ENSG00000143420 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1397598602 Functional Loss SNV dbSNP153 33..33 33 - - - 36577 RMVar_ID_36577 Human_SNP_ID_33454337 A-to-I Human chr1 - 150613222 150613222 150613222 AGTGTTGCTCTTGTTTCCCAGGCTGGAGAGCAATGGCGCAATCTCGGCTCACTGCAACCTCCACC AGTGTTGCTCTTGTTTCCCAGGCTGGAGAGCAGTGGCGCAATCTCGGCTCACTGCAACCTCCACC T C ENSA Ensembl:ENSG00000143420 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs918704666 Functional Loss SNV dbSNP153 33..33 33 - - - 36578 RMVar_ID_36578 Human_SNP_ID_33454625 A-to-I Human chr1 - 150614507 150614507 150614507 AAAAAATTAAAAAATTAGCCATGCATGATGGCATGCACCTGTGGCCCCAGCTACGTGGGAGGCTG AAAAAATTAAAAAATTAGCCATGCATGATGGCGTGCACCTGTGGCCCCAGCTACGTGGGAGGCTG T C ENSA Ensembl:ENSG00000143420 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1339847764 Functional Loss SNV dbSNP153 33..33 33 - - - 36579 RMVar_ID_36579 Human_SNP_ID_33454634 A-to-I Human chr1 - 150614548 150614547 150614548 GAGACCACCCTGGGCAACAAAATGAGACCCCCATCTCTACAAAAAAATTAAAAAATTAGCCATGC GAGACCACCCTGGGCAACAAAATGAGACCCCC_TCTCTACAAAAAAATTAAAAAATTAGCCATGC AT A ENSA Ensembl:ENSG00000143420 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1250977326 Functional Loss DEL dbSNP153 33..33 33 - - - 36580 RMVar_ID_36580 Human_SNP_ID_33454636 A-to-I Human chr1 - 150614548 150614548 150614548 GAGACCACCCTGGGCAACAAAATGAGACCCCCATCTCTACAAAAAAATTAAAAAATTAGCCATGC GAGACCACCCTGGGCAACAAAATGAGACCCCCGTCTCTACAAAAAAATTAAAAAATTAGCCATGC T C ENSA Ensembl:ENSG00000143420 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1370404478 Functional Loss SNV dbSNP153 33..33 33 - - - 36581 RMVar_ID_36581 Human_SNP_ID_33454637 A-to-I Human chr1 - 150614564 150614558 150614564 TTGTGCCCAGGAGTTCGAGACCACCCTGGGCAACAAAATGAGACCCCCATCTCTACAAAAAAATT TTGTGCCCAGGAGTTCGAGACCACCCTGGGCA______TGAGACCCCCATCTCTACAAAAAAATT ATTTTGT A ENSA Ensembl:ENSG00000143420 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1178923924 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_5687542 36582 RMVar_ID_36582 Human_SNP_ID_33454931 A-to-I Human chr1 - 150615553 150615553 150615553 AAAATAAAAGCCAGGCATGGTGGCACACGCCTATAGTCCCAGCTACTTGGGACGGTGAGGTAGGA AAAATAAAAGCCAGGCATGGTGGCACACGCCTGTAGTCCCAGCTACTTGGGACGGTGAGGTAGGA T C ENSA Ensembl:ENSG00000143420 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs758483190 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24751679 36583 RMVar_ID_36583 Human_SNP_ID_33454961 A-to-I Human chr1 - 150615682 150615682 150615682 AGGAGGGGCGGAGCCCAATGACTCAGGCGCCTATAATCCCGACAGTTTGGGAGGCTGAGGCAGGA AGGAGGGGCGGAGCCCAATGACTCAGGCGCCTGTAATCCCGACAGTTTGGGAGGCTGAGGCAGGA T C ENSA Ensembl:ENSG00000143420 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1427445686 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10572302 36584 RMVar_ID_36584 Human_SNP_ID_33455395 A-to-I Human chr1 - 150617348 150617348 150617348 CGTCACTGTACTCCAGCCTGGGCAACAAGAGCAAAACTCTGTCTCCAAAAAAAAAATAAAACATG CGTCACTGTACTCCAGCCTGGGCAACAAGAGCGAAACTCTGTCTCCAAAAAAAAAATAAAACATG T C ENSA Ensembl:ENSG00000143420 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs587740427 Functional Loss SNV dbSNP153 33..33 33 - - - 36585 RMVar_ID_36585 Human_SNP_ID_33455410 A-to-I Human chr1 - 150617391 150617391 150617391 TTGCTTGAACCCGGGAGGCGGAGGTTGCAGTGAGCCGAGATTGCGTCACTGTACTCCAGCCTGGG TTGCTTGAACCCGGGAGGCGGAGGTTGCAGTGGGCCGAGATTGCGTCACTGTACTCCAGCCTGGG T C ENSA Ensembl:ENSG00000143420 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1180864360 Functional Loss SNV dbSNP153 33..33 33 - - - 36586 RMVar_ID_36586 Human_SNP_ID_33455572 A-to-I Human chr1 - 150617942 150617942 150617942 AATACAAAAATTAGCCAGGCCTGGTGGCGGGTACCTGTAATCCCAGATACTCCGCAAGCTAAGGC AATACAAAAATTAGCCAGGCCTGGTGGCGGGTGCCTGTAATCCCAGATACTCCGCAAGCTAAGGC T C ENSA Ensembl:ENSG00000143420 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1295438579 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10572382 36587 RMVar_ID_36587 Human_SNP_ID_33455779 A-to-I Human chr1 - 150618483 150618483 150618483 CACCACCATGCCCGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTTGCCATGTTGGCCAGGC CACCACCATGCCCGGCTAATTTTTGTATTTTTGGTAGAGACGGGGTTTTGCCATGTTGGCCAGGC T C ENSA Ensembl:ENSG00000143420 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1168630447 Functional Loss SNV dbSNP153 33..33 33 - - - 36588 RMVar_ID_36588 Human_SNP_ID_33455802 A-to-I Human chr1 - 150618619 150618619 150618619 GTTTTTGAGGCAAGGTCTTGCTCTGTTGCCCAAGCTGGAGTGCAGTGGTGTGATCTCAGCTCACT GTTTTTGAGGCAAGGTCTTGCTCTGTTGCCCATGCTGGAGTGCAGTGGTGTGATCTCAGCTCACT T A ENSA Ensembl:ENSG00000143420 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs587680827 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23143907 36589 RMVar_ID_36589 Human_SNP_ID_33455828 A-to-I Human chr1 - 150618715 150618715 150618715 CACCTGCCTCAGCCTCCCAAAGTGCTAGGATTACAGATGTGAGCCACCGCGCCTGGCTGTGGTTT CACCTGCCTCAGCCTCCCAAAGTGCTAGGATTGCAGATGTGAGCCACCGCGCCTGGCTGTGGTTT T C ENSA Ensembl:ENSG00000143420 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1167985124 Functional Loss SNV dbSNP153 33..33 33 - - - 36590 RMVar_ID_36590 Human_SNP_ID_33455829 A-to-I Human chr1 - 150618721 150618721 150618721 GTGATCCACCTGCCTCAGCCTCCCAAAGTGCTAGGATTACAGATGTGAGCCACCGCGCCTGGCTG GTGATCCACCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGATGTGAGCCACCGCGCCTGGCTG T C ENSA Ensembl:ENSG00000143420 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1444859255 Functional Loss SNV dbSNP153 33..33 33 - - - 36591 RMVar_ID_36591 Human_SNP_ID_33455849 A-to-I Human chr1 - 150618789 150618789 150618789 TTTTGTACTTTTAGTAGAGACGGGGTTTCGCCATGTTGCCCTGGCTGGTCTTGAACTCCTGACCT TTTTGTACTTTTAGTAGAGACGGGGTTTCGCCGTGTTGCCCTGGCTGGTCTTGAACTCCTGACCT T C ENSA Ensembl:ENSG00000143420 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs587670362 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24585104 36592 RMVar_ID_36592 Human_SNP_ID_33455855 A-to-I Human chr1 - 150618806 150618806 150618806 CACCACACCTGGCTAATTTTTGTACTTTTAGTAGAGACGGGGTTTCGCCATGTTGCCCTGGCTGG CACCACACCTGGCTAATTTTTGTACTTTTAGTGGAGACGGGGTTTCGCCATGTTGCCCTGGCTGG T C ENSA Ensembl:ENSG00000143420 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs938914028 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10572396 36593 RMVar_ID_36593 Human_SNP_ID_33455858 A-to-I Human chr1 - 150618809 150618809 150618809 TGCCACCACACCTGGCTAATTTTTGTACTTTTAGTAGAGACGGGGTTTCGCCATGTTGCCCTGGC TGCCACCACACCTGGCTAATTTTTGTACTTTTCGTAGAGACGGGGTTTCGCCATGTTGCCCTGGC T G ENSA Ensembl:ENSG00000143420 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1238188375 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10572396 36594 RMVar_ID_36594 Human_SNP_ID_33455877 A-to-I Human chr1 - 150618915 150618913 150618915 CAGGCTGGAGTGCAGTAGTGAGATCTCAACTCACTGCAACCTCTGCCTCCTGGGTTCAAGCTATT CAGGCTGGAGTGCAGTAGTGAGATCTCAACTC__TGCAACCTCTGCCTCCTGGGTTCAAGCTATT AGT A ENSA Ensembl:ENSG00000143420 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1187797466 Functional Loss DEL dbSNP153 33..34 33 - - - 36595 RMVar_ID_36595 Human_SNP_ID_33455888 A-to-I Human chr1 - 150618965 150618963 150618965 GGCCTGTTGGTTTTTTTTTCTTTTTAAGACAGAGTCTCACTCTTGTCGCCCAGGCTGGAGTGCAG GGCCTGTTGGTTTTTTTTTCTTTTTAAGACAG__TCTCACTCTTGTCGCCCAGGCTGGAGTGCAG ACT A ENSA Ensembl:ENSG00000143420 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1356067901 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_10572398 36596 RMVar_ID_36596 Human_SNP_ID_33455924 A-to-I Human chr1 - 150619128 150619128 150619128 GGGATTACAGGCATGTGCCACCATGCCCTGCTAATTTTTGTATTTTTGGTAGAGATGGTGTATCA GGGATTACAGGCATGTGCCACCATGCCCTGCTGATTTTTGTATTTTTGGTAGAGATGGTGTATCA T C ENSA Ensembl:ENSG00000143420 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs745559265 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10572399 36597 RMVar_ID_36597 Human_SNP_ID_33455931 A-to-I Human chr1 - 150619171 150619171 150619171 ACCTCTGGGTTCAAGTGATTCTGCCTCACCCTACGGAGTAGCTGGGATTACAGGCATGTGCCACC ACCTCTGGGTTCAAGTGATTCTGCCTCACCCTGCGGAGTAGCTGGGATTACAGGCATGTGCCACC T C ENSA Ensembl:ENSG00000143420 Protein coding intron GSE100210;GSE107867;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank;ASD brains,frontal_cortex - 29129909,30559470,30559470 RNA-Seq:(High) rs943130562 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5687591,Human_RBP_ID_9456449 36598 RMVar_ID_36598 Human_SNP_ID_33456290 A-to-I Human chr1 - 150620724 150620724 150620724 GTTGTGTAGGCTGCTCCTGAACTCCTGGCCTCAAGCAGTCTTTCCACCTCAGCCTCCCAAAGTGC GTTGTGTAGGCTGCTCCTGAACTCCTGGCCTCGAGCAGTCTTTCCACCTCAGCCTCCCAAAGTGC T C ENSA Ensembl:ENSG00000143420 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs773189457 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3992183,Human_RBP_ID_8284834,Human_RBP_ID_10572479 36599 RMVar_ID_36599 Human_SNP_ID_33456339 A-to-I Human chr1 - 150620983 150620983 150620983 GCCTCAACCTCCTGGGCTCAAGTAATCTTCCCATCTCAGCCTCCCAAGTAGCTGGGACTACAAGC GCCTCAACCTCCTGGGCTCAAGTAATCTTCCCTTCTCAGCCTCCCAAGTAGCTGGGACTACAAGC T A ENSA Ensembl:ENSG00000143420 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1225465039 Functional Loss SNV dbSNP153 33..33 33 - - - 36600 RMVar_ID_36600 Human_SNP_ID_33456345 A-to-I Human chr1 - 150621021 150621018 150621022 CACCCAGAATGGAGTGCAGGGTGCAAACACTCACTGTAGCCTCAACCTCCTGGGCTCAAGTAATC CACCCAGAATGGAGTGCAGGGTGCAAACACT____GTAGCCTCAACCTCCTGGGCTCAAGTAATC CAGTG C ENSA Ensembl:ENSG00000143420 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs892687247 Functional Loss DEL dbSNP153 32..35 33 - - - 36601 RMVar_ID_36601 Human_SNP_ID_33456489 A-to-I Human chr1 - 150621482 150621482 150621482 ATCACTTGAGGTCAGGAGTTTGAGACCAGCCTAGCCAACATGGTGAAACCCCATCTCTACTAAAA ATCACTTGAGGTCAGGAGTTTGAGACCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAA T C ENSA Ensembl:ENSG00000143420 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs587594472 Functional Loss SNV dbSNP153 33..33 33 - - - 36602 RMVar_ID_36602 Human_SNP_ID_33456506 A-to-I Human chr1 - 150621547 150621547 150621547 ACTCCAGCGGGTGTACGGTGGCTCACGCCTATAATTCCAGCACTTTGGGAGGCCAAGGTGGGTGG ACTCCAGCGGGTGTACGGTGGCTCACGCCTATCATTCCAGCACTTTGGGAGGCCAAGGTGGGTGG T G ENSA Ensembl:ENSG00000143420 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1254605425 Functional Loss SNV dbSNP153 33..33 33 - - - 36603 RMVar_ID_36603 Human_SNP_ID_33456507 A-to-I Human chr1 - 150621549 150621549 150621549 AAACTCCAGCGGGTGTACGGTGGCTCACGCCTATAATTCCAGCACTTTGGGAGGCCAAGGTGGGT AAACTCCAGCGGGTGTACGGTGGCTCACGCCTGTAATTCCAGCACTTTGGGAGGCCAAGGTGGGT T C ENSA Ensembl:ENSG00000143420 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1016829948 Functional Loss SNV dbSNP153 33..33 33 - - - 36604 RMVar_ID_36604 Human_SNP_ID_33460618 A-to-I Human chr1 + 150637341 150637341 150637341 ATGGGCCAGGCTGGTCTTGAACTCCTGACCTTAGGCGATTCACCCGCCTCGGCCTCCCAAAGTGC ATGGGCCAGGCTGGTCTTGAACTCCTGACCTTGGGCGATTCACCCGCCTCGGCCTCCCAAAGTGC A G lnc-ADAMTSL4-7,lnc-ADAMTSL4-7:2 RNACentral:URS0000D58933,RNACentral:URS0000D5BD46 lincRNA,lincRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1395900167 Functional Loss SNV dbSNP153 33..33 33 - - - 36605 RMVar_ID_36605 Human_SNP_ID_33469550 A-to-I Human chr1 - 150676066 150676066 150676066 AGGAGGCTGAGGCCAGACGATTGTTTGAGTCTAGGAGGTTGGGGCTACAGTGAGCCATGTTCACA AGGAGGCTGAGGCCAGACGATTGTTTGAGTCTCGGAGGTTGGGGCTACAGTGAGCCATGTTCACA T G GOLPH3L Ensembl:ENSG00000143457 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs587689187 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93444,RMVar_hsa_circ_135927,RMVar_hsa_circ_75597,RMVar_hsa_circ_135926,RMVar_hsa_circ_45177 36606 RMVar_ID_36606 Human_SNP_ID_33469718 A-to-I Human chr1 - 150676808 150676808 150676808 GAAACCCAGTCTCTACTAAAAATACAAAAATTAGCCAGGCTTGGTGGCGGGTGGCTGTAATCCCA GAAACCCAGTCTCTACTAAAAATACAAAAATTTGCCAGGCTTGGTGGCGGGTGGCTGTAATCCCA T A GOLPH3L Ensembl:ENSG00000143457 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs587752244 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93444,RMVar_hsa_circ_135927,RMVar_hsa_circ_75597,RMVar_hsa_circ_135926,RMVar_hsa_circ_45177 36607 RMVar_ID_36607 Human_SNP_ID_33471642 A-to-I Human chr1 - 150684819 150684819 150684819 TACTAATAATACAAAAATTAGCTGGGCGTGGTAGTGCATGCCCGTAATCCCAGCTACTTGGGAGG TACTAATAATACAAAAATTAGCTGGGCGTGGTGGTGCATGCCCGTAATCCCAGCTACTTGGGAGG T C GOLPH3L Ensembl:ENSG00000143457 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs996041128 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93444,RMVar_hsa_circ_135927,RMVar_hsa_circ_75597,RMVar_hsa_circ_135926,RMVar_hsa_circ_45177 36608 RMVar_ID_36608 Human_SNP_ID_33472905 A-to-I Human chr1 - 150691034 150691034 150691034 CTGCCTTGGCCTCCCAAAGTGCTGGGATTACAAGCGTGAGCCACTGCACCTGGGCCATAGATCTT CTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCACCTGGGCCATAGATCTT T C GOLPH3L Ensembl:ENSG00000143457 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031698892 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93444,RMVar_hsa_circ_135927,RMVar_hsa_circ_75597,RMVar_hsa_circ_135926,RMVar_hsa_circ_45177 36609 RMVar_ID_36609 Human_SNP_ID_33482824 A-to-I Human chr1 - 150731144 150731144 150731144 ACCTCAGGTGATCCACCCACCCCAGCCTCCCAAAGTGCTAAGATTACAGGCGTGAGCCACTGAGC ACCTCAGGTGATCCACCCACCCCAGCCTCCCAGAGTGCTAAGATTACAGGCGTGAGCCACTGAGC T C CTSS Ensembl:ENSG00000163131 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1373084183 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85933,RMVar_hsa_circ_103543,RMVar_hsa_circ_135932,RMVar_hsa_circ_135933 36610 RMVar_ID_36610 Human_SNP_ID_33482841 A-to-I Human chr1 - 150731216 150731215 150731216 GCCCAGCTAATTTTTGTATTTTTAGTAAAGACAGGGTTTTGCCACATTAGCCAGGCTGGTCTCAA GCCCAGCTAATTTTTGTATTTTTAGTAAAGAC_GGGTTTTGCCACATTAGCCAGGCTGGTCTCAA CT C CTSS Ensembl:ENSG00000163131 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1254758779 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_85933,RMVar_hsa_circ_103543,RMVar_hsa_circ_135932,RMVar_hsa_circ_135933 36611 RMVar_ID_36611 Human_SNP_ID_33482843 A-to-I Human chr1 - 150731231 150731231 150731231 GGCGTGCACCACCACGCCCAGCTAATTTTTGTATTTTTAGTAAAGACAGGGTTTTGCCACATTAG GGCGTGCACCACCACGCCCAGCTAATTTTTGTGTTTTTAGTAAAGACAGGGTTTTGCCACATTAG T C CTSS Ensembl:ENSG00000163131 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs926249787 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85933,RMVar_hsa_circ_103543,RMVar_hsa_circ_135932,RMVar_hsa_circ_135933 36612 RMVar_ID_36612 Human_SNP_ID_33482858 A-to-I Human chr1 - 150731311 150731311 150731311 CCATCTCAGTTCACTGCAACTTCTGCCTCCCGAGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGA CCATCTCAGTTCACTGCAACTTCTGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGA T C CTSS Ensembl:ENSG00000163131 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs56091952 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_98429 RMVar_hsa_circ_85933,RMVar_hsa_circ_103543,RMVar_hsa_circ_135932,RMVar_hsa_circ_135933 36613 RMVar_ID_36613 Human_SNP_ID_33482870 A-to-I Human chr1 - 150731362 150731362 150731362 GTTTTTTGAGACGGAGTCTCACTCTGTTGCCCAGGCTGGAGTGCAGTGGCACCATCTCAGTTCAC GTTTTTTGAGACGGAGTCTCACTCTGTTGCCCGGGCTGGAGTGCAGTGGCACCATCTCAGTTCAC T C CTSS Ensembl:ENSG00000163131 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1485858584 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85933,RMVar_hsa_circ_103543,RMVar_hsa_circ_135932,RMVar_hsa_circ_135933 36614 RMVar_ID_36614 Human_SNP_ID_33482872 A-to-I Human chr1 - 150731374 150731374 150731374 CAGTTTTGTTTTGTTTTTTGAGACGGAGTCTCACTCTGTTGCCCAGGCTGGAGTGCAGTGGCACC CAGTTTTGTTTTGTTTTTTGAGACGGAGTCTCGCTCTGTTGCCCAGGCTGGAGTGCAGTGGCACC T C CTSS Ensembl:ENSG00000163131 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1048111395 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85933,RMVar_hsa_circ_103543,RMVar_hsa_circ_135932,RMVar_hsa_circ_135933 36615 RMVar_ID_36615 Human_SNP_ID_33482961 A-to-I Human chr1 - 150731937 150731937 150731937 GCACCACTGCACTCCAGCCTGGGTGACAGAGCAAGACCCTGTCTTAAAAAAAGAGGATTCAACAC GCACCACTGCACTCCAGCCTGGGTGACAGAGCGAGACCCTGTCTTAAAAAAAGAGGATTCAACAC T C CTSS Ensembl:ENSG00000163131 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1052341770 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85933,RMVar_hsa_circ_103543,RMVar_hsa_circ_135932,RMVar_hsa_circ_135933 36616 RMVar_ID_36616 Human_SNP_ID_33482978 A-to-I Human chr1 - 150732007 150732007 150732007 GCTATGCAGATGTCTAAGACAGGAGGATCACAAGAGCCCAGGAGGTTGAGAATGCAGTGAGCTTG GCTATGCAGATGTCTAAGACAGGAGGATCACAGGAGCCCAGGAGGTTGAGAATGCAGTGAGCTTG T C CTSS Ensembl:ENSG00000163131 Protein coding 3'UTR GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1259374528 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85933,RMVar_hsa_circ_103543,RMVar_hsa_circ_135932,RMVar_hsa_circ_135933,RMVar_hsa_circ_135934 36617 RMVar_ID_36617 Human_SNP_ID_33483009 A-to-I Human chr1 - 150732177 150732177 150732177 GCCACGTGTAGTGGCTCATGCCTGTAATCCCAACACTTTGGGAGGCTGAAGTAGGAGGATCGTCT GCCACGTGTAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAAGTAGGAGGATCGTCT T C CTSS Ensembl:ENSG00000163131 Protein coding 3'UTR GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs898311674 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85933,RMVar_hsa_circ_103543,RMVar_hsa_circ_135932,RMVar_hsa_circ_135933 36618 RMVar_ID_36618 Human_SNP_ID_33483010 A-to-I Human chr1 - 150732178 150732178 150732178 CGCCACGTGTAGTGGCTCATGCCTGTAATCCCAACACTTTGGGAGGCTGAAGTAGGAGGATCGTC CGCCACGTGTAGTGGCTCATGCCTGTAATCCCGACACTTTGGGAGGCTGAAGTAGGAGGATCGTC T C CTSS Ensembl:ENSG00000163131 Protein coding 3'UTR GSE47997;GSE38233;GSE38233 K562 cells&HepG2 cells;cultured B-cells;cultured B-cells - 23474544,24183664,24183664 RNA-Seq:(High) rs1211422458 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85933,RMVar_hsa_circ_103543,RMVar_hsa_circ_135932,RMVar_hsa_circ_135933 36619 RMVar_ID_36619 Human_SNP_ID_33483122 A-to-I Human chr1 - 150732784 150732784 150732784 GCTAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAAATTAGCCGAGCACGGTGGTGCATG GCTAACATGGTGAAACCCCATCTCTACTAAAATTACAAAAAATTAGCCGAGCACGGTGGTGCATG T A CTSS Ensembl:ENSG00000163131 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1364191064 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85933,RMVar_hsa_circ_103543,RMVar_hsa_circ_135932,RMVar_hsa_circ_135933 36620 RMVar_ID_36620 Human_SNP_ID_33483125 A-to-I Human chr1 - 150732797 150732797 150732797 AAAGAGCAGCCTGGCTAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAAATTAGCCGAGC AAAGAGCAGCCTGGCTAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTAGCCGAGC T C CTSS Ensembl:ENSG00000163131 Protein coding 3'UTR GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1436787632 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_98431 RMVar_hsa_circ_85933,RMVar_hsa_circ_103543,RMVar_hsa_circ_135932,RMVar_hsa_circ_135933 36621 RMVar_ID_36621 Human_SNP_ID_33483127 A-to-I Human chr1 - 150732802 150732802 150732802 GAGTTAAAGAGCAGCCTGGCTAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAAATTAGC GAGTTAAAGAGCAGCCTGGCTAACATGGTGAAGCCCCATCTCTACTAAAAATACAAAAAATTAGC T C CTSS Ensembl:ENSG00000163131 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs3208233 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_98431 RMVar_hsa_circ_85933,RMVar_hsa_circ_103543,RMVar_hsa_circ_135932,RMVar_hsa_circ_135933 36622 RMVar_ID_36622 Human_SNP_ID_33483136 A-to-I Human chr1 - 150732861 150732861 150732861 CTCACGCCTGTAATCCCAGTACTTGGGAGGCCAAGGCAGGCATATCAACTTGAGGCCAGGAGTTA CTCACGCCTGTAATCCCAGTACTTGGGAGGCCGAGGCAGGCATATCAACTTGAGGCCAGGAGTTA T C CTSS Ensembl:ENSG00000163131 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1190956080 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85933,RMVar_hsa_circ_103543,RMVar_hsa_circ_135932,RMVar_hsa_circ_135933 36623 RMVar_ID_36623 Human_SNP_ID_33484342 A-to-I Human chr1 - 150739081 150739081 150739081 TAAGCAATTCTCCTGCCTCAGCCTCCGGAGTAACTGGGATTACAGGCACGCACCACCACACCCTG TAAGCAATTCTCCTGCCTCAGCCTCCGGAGTAGCTGGGATTACAGGCACGCACCACCACACCCTG T C CTSS Ensembl:ENSG00000163131 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs113967546 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_4052,GWAS_ID_4053,GWAS_ID_4054,GWAS_ID_4055,GWAS_ID_4056,GWAS_ID_4057,GWAS_ID_4058,GWAS_ID_4059,GWAS_ID_4060,GWAS_ID_4061,GWAS_ID_4062,GWAS_ID_4063 RMVar_hsa_circ_85933,RMVar_hsa_circ_103543,RMVar_hsa_circ_135932,RMVar_hsa_circ_135933 36624 RMVar_ID_36624 Human_SNP_ID_33484732 A-to-I Human chr1 - 150740864 150740864 150740864 GGGGAACATAGTGAGACCCCATCTCTATACAAAAATAAGCCAGGCATGGTGACACACACTTGTGG GGGGAACATAGTGAGACCCCATCTCTATACAAGAATAAGCCAGGCATGGTGACACACACTTGTGG T C CTSS Ensembl:ENSG00000163131 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1381142318 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85933,RMVar_hsa_circ_103543,RMVar_hsa_circ_135932,RMVar_hsa_circ_135933 36625 RMVar_ID_36625 Human_SNP_ID_33484787 A-to-I Human chr1 - 150741126 150741126 150741126 ATGGTGGCATGTGCCTGTAATATCAACTACTCAAGAGGCTGAGGTAGGAGGATTTTTTGAGCTGA ATGGTGGCATGTGCCTGTAATATCAACTACTCGAGAGGCTGAGGTAGGAGGATTTTTTGAGCTGA T C CTSS Ensembl:ENSG00000163131 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs956400193 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85933,RMVar_hsa_circ_103543,RMVar_hsa_circ_135932,RMVar_hsa_circ_135933 36626 RMVar_ID_36626 Human_SNP_ID_33484789 A-to-I Human chr1 - 150741137 150741137 150741137 ATTAGCTGGGCATGGTGGCATGTGCCTGTAATATCAACTACTCAAGAGGCTGAGGTAGGAGGATT ATTAGCTGGGCATGGTGGCATGTGCCTGTAATGTCAACTACTCAAGAGGCTGAGGTAGGAGGATT T C CTSS Ensembl:ENSG00000163131 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs914841573 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85933,RMVar_hsa_circ_103543,RMVar_hsa_circ_135932,RMVar_hsa_circ_135933 36627 RMVar_ID_36627 Human_SNP_ID_33484790 A-to-I Human chr1 - 150741140 150741140 150741140 AAAATTAGCTGGGCATGGTGGCATGTGCCTGTAATATCAACTACTCAAGAGGCTGAGGTAGGAGG AAAATTAGCTGGGCATGGTGGCATGTGCCTGTTATATCAACTACTCAAGAGGCTGAGGTAGGAGG T A CTSS Ensembl:ENSG00000163131 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs183345008 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85933,RMVar_hsa_circ_103543,RMVar_hsa_circ_135932,RMVar_hsa_circ_135933 36628 RMVar_ID_36628 Human_SNP_ID_33484791 A-to-I Human chr1 - 150741140 150741140 150741140 AAAATTAGCTGGGCATGGTGGCATGTGCCTGTAATATCAACTACTCAAGAGGCTGAGGTAGGAGG AAAATTAGCTGGGCATGGTGGCATGTGCCTGTGATATCAACTACTCAAGAGGCTGAGGTAGGAGG T C CTSS Ensembl:ENSG00000163131 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs183345008 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85933,RMVar_hsa_circ_103543,RMVar_hsa_circ_135932,RMVar_hsa_circ_135933 36629 RMVar_ID_36629 Human_SNP_ID_33484977 A-to-I Human chr1 - 150741994 150741994 150741994 GACCTCGTGATCTGCCCACCTCGGTCTCCCCAAGTGCTGGGATTACAGGCATGAGCCACCCTACC GACCTCGTGATCTGCCCACCTCGGTCTCCCCAGGTGCTGGGATTACAGGCATGAGCCACCCTACC T C CTSS Ensembl:ENSG00000163131 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs919300788 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85933,RMVar_hsa_circ_103543,RMVar_hsa_circ_135932,RMVar_hsa_circ_135933 36630 RMVar_ID_36630 Human_SNP_ID_33504932 A-to-I Human chr1 - 150826190 150826190 150826190 TTTTCCTCGTCTGGGCATGGTGGCTCACGCCTATAATCCCAGCACTCTGGGAGGCTGAGGCAGGT TTTTCCTCGTCTGGGCATGGTGGCTCACGCCTGTAATCCCAGCACTCTGGGAGGCTGAGGCAGGT T C ARNT Ensembl:ENSG00000143437 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs587716774 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106973,RMVar_hsa_circ_135939,RMVar_hsa_circ_368934,RMVar_hsa_circ_330599,RMVar_hsa_circ_55700,RMVar_hsa_circ_75265,RMVar_hsa_circ_288189,RMVar_hsa_circ_135943,RMVar_hsa_circ_290315,RMVar_hsa_circ_301368,RMVar_hsa_circ_344445,RMVar_hsa_circ_360755,RMVar_hsa_circ_292504,RMVar_hsa_circ_92823,RMVar_hsa_circ_135945,RMVar_hsa_circ_135947,RMVar_hsa_circ_51901,RMVar_hsa_circ_135948,RMVar_hsa_circ_135946,RMVar_hsa_circ_135944 36631 RMVar_ID_36631 Human_SNP_ID_33505741 A-to-I Human chr1 - 150829925 150829925 150829925 CCAGAGGCTGGCCAGGGAAGCAAGTTTTGCCTAGTGGCCATTGGCAGATTGCAGGCAAGTATGAA CCAGAGGCTGGCCAGGGAAGCAAGTTTTGCCTGGTGGCCATTGGCAGATTGCAGGCAAGTATGAA T C ARNT Ensembl:ENSG00000143437 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs777035487 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_858430,Human_RBP_ID_5157329,Human_RBP_ID_19035297 Human_Splice_Rec_127234,Human_Splice_Rec_127274,Human_Splice_Rec_127302,Human_Splice_Rec_127344,Human_Splice_Rec_127382,Human_Splice_Rec_127410 Human_miRNA_ID_2673899,Human_miRNA_ID_2924655 RMVar_hsa_circ_19964,RMVar_hsa_circ_106973,RMVar_hsa_circ_135939,RMVar_hsa_circ_368934,RMVar_hsa_circ_75265,RMVar_hsa_circ_290315,RMVar_hsa_circ_301368,RMVar_hsa_circ_344445,RMVar_hsa_circ_360755,RMVar_hsa_circ_92823,RMVar_hsa_circ_135945,RMVar_hsa_circ_135947,RMVar_hsa_circ_135948,RMVar_hsa_circ_135946,RMVar_hsa_circ_48220,RMVar_hsa_circ_343876,RMVar_hsa_circ_365196,RMVar_hsa_circ_347344,RMVar_hsa_circ_296176,RMVar_hsa_circ_22904,RMVar_hsa_circ_135949,RMVar_hsa_circ_327695,RMVar_hsa_circ_346565 36632 RMVar_ID_36632 Human_SNP_ID_33506439 A-to-I Human chr1 - 150833286 150833286 150833286 TTGGCCAGGCTGGCCTCAAACTCTTGACCTCAAGTGATTCGCCTGCGTCAGCCTCCCAAAGTGCT TTGGCCAGGCTGGCCTCAAACTCTTGACCTCATGTGATTCGCCTGCGTCAGCCTCCCAAAGTGCT T A ARNT Ensembl:ENSG00000143437 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1312348801 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19964,RMVar_hsa_circ_368934,RMVar_hsa_circ_75265,RMVar_hsa_circ_290315,RMVar_hsa_circ_301368,RMVar_hsa_circ_344445,RMVar_hsa_circ_92823,RMVar_hsa_circ_135947,RMVar_hsa_circ_135948,RMVar_hsa_circ_135946,RMVar_hsa_circ_48220,RMVar_hsa_circ_365196,RMVar_hsa_circ_296176,RMVar_hsa_circ_22904,RMVar_hsa_circ_57485,RMVar_hsa_circ_135949,RMVar_hsa_circ_327695,RMVar_hsa_circ_346565,RMVar_hsa_circ_344680,RMVar_hsa_circ_65567,RMVar_hsa_circ_41097,RMVar_hsa_circ_52711,RMVar_hsa_circ_32058,RMVar_hsa_circ_356357 36633 RMVar_ID_36633 Human_SNP_ID_33509060 A-to-I Human chr1 - 150845486 150845486 150845486 CTTCCACCTCAGCCTCCCTAGTAGCTGGGAATATGGGCATTTGCCACCATGCCTAGCTAATTTTT CTTCCACCTCAGCCTCCCTAGTAGCTGGGAATGTGGGCATTTGCCACCATGCCTAGCTAATTTTT T C ARNT Ensembl:ENSG00000143437 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1041997537 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19964,RMVar_hsa_circ_75265,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_54627,RMVar_hsa_circ_72829,RMVar_hsa_circ_85968,RMVar_hsa_circ_135954 36634 RMVar_ID_36634 Human_SNP_ID_33510136 A-to-I Human chr1 - 150849877 150849877 150849877 TATTTTTAGTAGAGACGGGGTTTCACCATGTTAGCCAGACTGGTCTTGAACTCTTGGCCTTAAGT TATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGACTGGTCTTGAACTCTTGGCCTTAAGT T C ARNT Ensembl:ENSG00000143437 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1437636775 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19964,RMVar_hsa_circ_75265,RMVar_hsa_circ_22904,RMVar_hsa_circ_4816,RMVar_hsa_circ_57485,RMVar_hsa_circ_344680,RMVar_hsa_circ_54627,RMVar_hsa_circ_72829,RMVar_hsa_circ_85968,RMVar_hsa_circ_135954,RMVar_hsa_circ_378953 36635 RMVar_ID_36635 Human_SNP_ID_33510160 A-to-I Human chr1 - 150849992 150849992 150849992 GCTGGAGTGCAGTGCTGCAGTCTTGGCTCACTACAACTTCTGCCTTCCAGGTTCAAGCGATTCTA GCTGGAGTGCAGTGCTGCAGTCTTGGCTCACTGCAACTTCTGCCTTCCAGGTTCAAGCGATTCTA T C ARNT Ensembl:ENSG00000143437 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs907767463 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19964,RMVar_hsa_circ_75265,RMVar_hsa_circ_22904,RMVar_hsa_circ_4816,RMVar_hsa_circ_57485,RMVar_hsa_circ_344680,RMVar_hsa_circ_54627,RMVar_hsa_circ_72829,RMVar_hsa_circ_85968,RMVar_hsa_circ_135954,RMVar_hsa_circ_378953 36636 RMVar_ID_36636 Human_SNP_ID_33515134 A-to-I Human chr1 - 150869088 150869088 150869088 GTCCTGTTGTGTCAGCCAGGCTGGAGTGCAGTAGCGTGACCATAGCTTCCTGCAACACCTCCAAT GTCCTGTTGTGTCAGCCAGGCTGGAGTGCAGTGGCGTGACCATAGCTTCCTGCAACACCTCCAAT T C ARNT Ensembl:ENSG00000143437 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1235553661 Functional Loss SNV dbSNP153 33..33 33 - - - 36637 RMVar_ID_36637 Human_SNP_ID_33515548 A-to-I Human chr1 - 150870949 150870948 150870949 TTGCCCCGGCTGGTCTCAAACTCCTGGGCTCAAGCAATCCTCCTGCCTCGGCCTCCCAGAGTGCC TTGCCCCGGCTGGTCTCAAACTCCTGGGCTCA_GCAATCCTCCTGCCTCGGCCTCCCAGAGTGCC CT C ARNT Ensembl:ENSG00000143437 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs920605226 Functional Loss DEL dbSNP153 33..33 33 - - - 36638 RMVar_ID_36638 Human_SNP_ID_33530632 A-to-I Human chr1 + 150930628 150930628 150930628 TCAGCTCACTGCAACCTCTGCCTCCTGGGTTCAAGCAATTCTCTGCTTCGACCTCCCAACTAGCT TCAGCTCACTGCAACCTCTGCCTCCTGGGTTCCAGCAATTCTCTGCTTCGACCTCCCAACTAGCT A C SETDB1 Ensembl:ENSG00000143379 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1453049070 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26368102 RMVar_hsa_circ_38707,RMVar_hsa_circ_353159,RMVar_hsa_circ_374033,RMVar_hsa_circ_347097,RMVar_hsa_circ_352777,RMVar_hsa_circ_331799,RMVar_hsa_circ_303013,RMVar_hsa_circ_279206,RMVar_hsa_circ_31669,RMVar_hsa_circ_340345,RMVar_hsa_circ_135958,RMVar_hsa_circ_135959,RMVar_hsa_circ_135960,RMVar_hsa_circ_341440,RMVar_hsa_circ_325821,RMVar_hsa_circ_334286,RMVar_hsa_circ_289020,RMVar_hsa_circ_135962,RMVar_hsa_circ_135963,RMVar_hsa_circ_135964,RMVar_hsa_circ_135961 36639 RMVar_ID_36639 Human_SNP_ID_33530708 A-to-I Human chr1 + 150930986 150930986 150930986 AGTGTTGAATAAGTTTTAAGAGCAGGCCAGATACAGTGGCTCATACCTGTAATCCCAGCACTTTG AGTGTTGAATAAGTTTTAAGAGCAGGCCAGATGCAGTGGCTCATACCTGTAATCCCAGCACTTTG A G SETDB1 Ensembl:ENSG00000143379 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs935011083 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38707,RMVar_hsa_circ_353159,RMVar_hsa_circ_374033,RMVar_hsa_circ_347097,RMVar_hsa_circ_352777,RMVar_hsa_circ_331799,RMVar_hsa_circ_303013,RMVar_hsa_circ_279206,RMVar_hsa_circ_31669,RMVar_hsa_circ_340345,RMVar_hsa_circ_135958,RMVar_hsa_circ_135959,RMVar_hsa_circ_135960,RMVar_hsa_circ_341440,RMVar_hsa_circ_325821,RMVar_hsa_circ_334286,RMVar_hsa_circ_289020,RMVar_hsa_circ_135962,RMVar_hsa_circ_135963,RMVar_hsa_circ_135964,RMVar_hsa_circ_135961 36640 RMVar_ID_36640 Human_SNP_ID_33530725 A-to-I Human chr1 + 150931053 150931053 150931053 AGGTTGAGGTGGGAGGATCCCCTGATCCCAGGAATTTGAGACCAGCCTGGCCAACGTAGCAAGAC AGGTTGAGGTGGGAGGATCCCCTGATCCCAGGTATTTGAGACCAGCCTGGCCAACGTAGCAAGAC A T SETDB1 Ensembl:ENSG00000143379 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1249918320 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10574151 RMVar_hsa_circ_38707,RMVar_hsa_circ_353159,RMVar_hsa_circ_374033,RMVar_hsa_circ_347097,RMVar_hsa_circ_352777,RMVar_hsa_circ_331799,RMVar_hsa_circ_303013,RMVar_hsa_circ_279206,RMVar_hsa_circ_31669,RMVar_hsa_circ_340345,RMVar_hsa_circ_135958,RMVar_hsa_circ_135959,RMVar_hsa_circ_135960,RMVar_hsa_circ_341440,RMVar_hsa_circ_325821,RMVar_hsa_circ_334286,RMVar_hsa_circ_289020,RMVar_hsa_circ_135962,RMVar_hsa_circ_135963,RMVar_hsa_circ_135964,RMVar_hsa_circ_135961 36641 RMVar_ID_36641 Human_SNP_ID_33531363 A-to-I Human chr1 + 150933129 150933129 150933129 TTCCCCAGGCTGGAGTGTGATAGCATGATCATAGTTCACTGCAGCCTCAACCTCCTGGGCTCAAG TTCCCCAGGCTGGAGTGTGATAGCATGATCATGGTTCACTGCAGCCTCAACCTCCTGGGCTCAAG A G SETDB1 Ensembl:ENSG00000143379 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs587760018 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10574181,Human_RBP_ID_23331716 RMVar_hsa_circ_38707,RMVar_hsa_circ_353159,RMVar_hsa_circ_374033,RMVar_hsa_circ_347097,RMVar_hsa_circ_352777,RMVar_hsa_circ_331799,RMVar_hsa_circ_303013,RMVar_hsa_circ_279206,RMVar_hsa_circ_31669,RMVar_hsa_circ_340345,RMVar_hsa_circ_135958,RMVar_hsa_circ_135959,RMVar_hsa_circ_135960,RMVar_hsa_circ_341440,RMVar_hsa_circ_325821,RMVar_hsa_circ_334286,RMVar_hsa_circ_289020,RMVar_hsa_circ_135962,RMVar_hsa_circ_135963,RMVar_hsa_circ_135964,RMVar_hsa_circ_135961 36642 RMVar_ID_36642 Human_SNP_ID_33532313 A-to-I Human chr1 + 150936741 150936741 150936741 AGTATCTCACTCTGTAACCCAGGCTGGAGCACAGTAGTGCTATCATAGCTCACTTCGACTTCAGC AGTATCTCACTCTGTAACCCAGGCTGGAGCACCGTAGTGCTATCATAGCTCACTTCGACTTCAGC A C SETDB1 Ensembl:ENSG00000143379 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs979793391 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10574213 RMVar_hsa_circ_38707,RMVar_hsa_circ_353159,RMVar_hsa_circ_374033,RMVar_hsa_circ_347097,RMVar_hsa_circ_352777,RMVar_hsa_circ_331799,RMVar_hsa_circ_303013,RMVar_hsa_circ_279206,RMVar_hsa_circ_31669,RMVar_hsa_circ_340345,RMVar_hsa_circ_135958,RMVar_hsa_circ_135959,RMVar_hsa_circ_135960,RMVar_hsa_circ_341440,RMVar_hsa_circ_325821,RMVar_hsa_circ_334286,RMVar_hsa_circ_289020,RMVar_hsa_circ_135962,RMVar_hsa_circ_135963,RMVar_hsa_circ_135964,RMVar_hsa_circ_135961 36643 RMVar_ID_36643 Human_SNP_ID_33532315 A-to-I Human chr1 + 150936744 150936744 150936744 ATCTCACTCTGTAACCCAGGCTGGAGCACAGTAGTGCTATCATAGCTCACTTCGACTTCAGCCTC ATCTCACTCTGTAACCCAGGCTGGAGCACAGTGGTGCTATCATAGCTCACTTCGACTTCAGCCTC A G SETDB1 Ensembl:ENSG00000143379 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1295835907 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10574214 RMVar_hsa_circ_38707,RMVar_hsa_circ_353159,RMVar_hsa_circ_374033,RMVar_hsa_circ_347097,RMVar_hsa_circ_352777,RMVar_hsa_circ_331799,RMVar_hsa_circ_303013,RMVar_hsa_circ_279206,RMVar_hsa_circ_31669,RMVar_hsa_circ_340345,RMVar_hsa_circ_135958,RMVar_hsa_circ_135959,RMVar_hsa_circ_135960,RMVar_hsa_circ_341440,RMVar_hsa_circ_325821,RMVar_hsa_circ_334286,RMVar_hsa_circ_289020,RMVar_hsa_circ_135962,RMVar_hsa_circ_135963,RMVar_hsa_circ_135964,RMVar_hsa_circ_135961 36644 RMVar_ID_36644 Human_SNP_ID_33532894 A-to-I Human chr1 + 150938994 150938994 150938994 CACTGGTCTTACGCTGCACCAAGCTGGAGTGCAATGGTGCAGTCTTGGCTTACTGCAACCCTTGC CACTGGTCTTACGCTGCACCAAGCTGGAGTGCGATGGTGCAGTCTTGGCTTACTGCAACCCTTGC A G SETDB1 Ensembl:ENSG00000143379 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1262231073 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38707,RMVar_hsa_circ_353159,RMVar_hsa_circ_374033,RMVar_hsa_circ_347097,RMVar_hsa_circ_352777,RMVar_hsa_circ_331799,RMVar_hsa_circ_303013,RMVar_hsa_circ_279206,RMVar_hsa_circ_31669,RMVar_hsa_circ_340345,RMVar_hsa_circ_135958,RMVar_hsa_circ_135959,RMVar_hsa_circ_135960,RMVar_hsa_circ_341440,RMVar_hsa_circ_325821,RMVar_hsa_circ_334286,RMVar_hsa_circ_289020,RMVar_hsa_circ_135962,RMVar_hsa_circ_135963,RMVar_hsa_circ_135964,RMVar_hsa_circ_135961 36645 RMVar_ID_36645 Human_SNP_ID_33537539 A-to-I Human chr1 + 150957245 150957245 150957245 CAAAAATTAGCAGGGTATGATGGCATGCACCTATAATCCCAGCTACTTGGGAGGCTGAGGCAGGA CAAAAATTAGCAGGGTATGATGGCATGCACCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGA A G SETDB1 Ensembl:ENSG00000143379 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1175864724 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38707,RMVar_hsa_circ_374033,RMVar_hsa_circ_347097,RMVar_hsa_circ_31669,RMVar_hsa_circ_340345,RMVar_hsa_circ_135960,RMVar_hsa_circ_135964,RMVar_hsa_circ_115912,RMVar_hsa_circ_56623,RMVar_hsa_circ_135966,RMVar_hsa_circ_72325,RMVar_hsa_circ_135969,RMVar_hsa_circ_86901,RMVar_hsa_circ_126533,RMVar_hsa_circ_135972,RMVar_hsa_circ_309524,RMVar_hsa_circ_79479,RMVar_hsa_circ_135975,RMVar_hsa_circ_310491,RMVar_hsa_circ_135978,RMVar_hsa_circ_84833,RMVar_hsa_circ_107353,RMVar_hsa_circ_371960,RMVar_hsa_circ_135980,RMVar_hsa_circ_279567,RMVar_hsa_circ_82026,RMVar_hsa_circ_135982,RMVar_hsa_circ_135983,RMVar_hsa_circ_135984,RMVar_hsa_circ_135981 36646 RMVar_ID_36646 Human_SNP_ID_33537723 A-to-I Human chr1 + 150958065 150958065 150958065 AAAATTAGCAAGGCACGGTGGCGCGTGCCTGTAATCTCAGCTACTTGGGAGGCTGAGGCAGGAGA AAAATTAGCAAGGCACGGTGGCGCGTGCCTGTCATCTCAGCTACTTGGGAGGCTGAGGCAGGAGA A C SETDB1 Ensembl:ENSG00000143379 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1481279361 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38707,RMVar_hsa_circ_374033,RMVar_hsa_circ_347097,RMVar_hsa_circ_31669,RMVar_hsa_circ_340345,RMVar_hsa_circ_135960,RMVar_hsa_circ_135964,RMVar_hsa_circ_115912,RMVar_hsa_circ_56623,RMVar_hsa_circ_135966,RMVar_hsa_circ_72325,RMVar_hsa_circ_135969,RMVar_hsa_circ_86901,RMVar_hsa_circ_126533,RMVar_hsa_circ_135972,RMVar_hsa_circ_309524,RMVar_hsa_circ_79479,RMVar_hsa_circ_135975,RMVar_hsa_circ_310491,RMVar_hsa_circ_135978,RMVar_hsa_circ_84833,RMVar_hsa_circ_107353,RMVar_hsa_circ_371960,RMVar_hsa_circ_135980,RMVar_hsa_circ_279567,RMVar_hsa_circ_82026,RMVar_hsa_circ_135982,RMVar_hsa_circ_135983,RMVar_hsa_circ_135984,RMVar_hsa_circ_135981 36647 RMVar_ID_36647 Human_SNP_ID_33539866 A-to-I Human chr1 + 150965451 150965451 150965451 TAGTTGCCATTCTACTCCAAACCAGCTAGCCTAGCTGAAGAGAAGAGGGAAGGGGGAAGAGGCCA TAGTTGCCATTCTACTCCAAACCAGCTAGCCTGGCTGAAGAGAAGAGGGAAGGGGGAAGAGGCCA A G AL590133.2 Ensembl:ENSG00000259357 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs769393868 Functional Loss SNV dbSNP153 33..33 33 - - - 36648 RMVar_ID_36648 Human_SNP_ID_33547452 A-to-I Human chr1 - 150993382 150993382 150993382 ATTGCTTGAACCTGGGAGGCGGACGTTGCAGTAAGCTGAGATCACACCACTGCACTCCAGCCTGG ATTGCTTGAACCTGGGAGGCGGACGTTGCAGTGAGCTGAGATCACACCACTGCACTCCAGCCTGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs3211289 Functional Loss SNV dbSNP153 33..33 33 - - - 36649 RMVar_ID_36649 Human_SNP_ID_33547464 A-to-I Human chr1 - 150993420 150993420 150993420 CCTATAATCCCAGCTACTGAGGAGGGTGAGGTAGGAGAATTGCTTGAACCTGGGAGGCGGACGTT CCTATAATCCCAGCTACTGAGGAGGGTGAGGTGGGAGAATTGCTTGAACCTGGGAGGCGGACGTT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs944018978 Functional Loss SNV dbSNP153 33..33 33 - - - 36650 RMVar_ID_36650 Human_SNP_ID_33547484 A-to-I Human chr1 - 150993486 150993486 150993486 GGCCAACATGGTGAAACCCCCGTCTCTATTAAAACTACAAAAATTAGCCAGGTGTGGTGGTAGGC GGCCAACATGGTGAAACCCCCGTCTCTATTAAGACTACAAAAATTAGCCAGGTGTGGTGGTAGGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs3211290 Functional Loss SNV dbSNP153 33..33 33 - - - 36651 RMVar_ID_36651 Human_SNP_ID_33548146 A-to-I Human chr1 - 150996182 150996182 150996182 GTCAGGCTAGTCTTGAATTCCTGACCTCAAGTAATCCGCCTGCCTTGGCCTCCCGAAGTGCTGGA GTCAGGCTAGTCTTGAATTCCTGACCTCAAGTGATCCGCCTGCCTTGGCCTCCCGAAGTGCTGGA T C MINDY1 Ensembl:ENSG00000143409 Protein coding 3'UTR GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 29129909,30559470 RNA-Seq:(High) rs967742693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557310,Human_RBP_ID_26388550 36652 RMVar_ID_36652 Human_SNP_ID_33548158 A-to-I Human chr1 - 150996238 150996238 150996238 CGCCACTGCGCCCAGCTAATTTTTGTATTTTTAGTAGAGACGGTTTCGCCACTTTGGTCAGGCTA CGCCACTGCGCCCAGCTAATTTTTGTATTTTTGGTAGAGACGGTTTCGCCACTTTGGTCAGGCTA T C MINDY1 Ensembl:ENSG00000143409 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1261910040 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557310,Human_RBP_ID_26388550 36653 RMVar_ID_36653 Human_SNP_ID_33548310 A-to-I Human chr1 - 150996726 150996726 150996726 CAGCCTGCCCAAAAAGGTGAAACCCCGTCTCTACTAAAAATACAAGAAATTAGCTGGGCGTCATG CAGCCTGCCCAAAAAGGTGAAACCCCGTCTCTGCTAAAAATACAAGAAATTAGCTGGGCGTCATG T C MINDY1 Ensembl:ENSG00000143409 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs587669220 Functional Loss SNV dbSNP153 33..33 33 - - - 36654 RMVar_ID_36654 Human_SNP_ID_33550247 A-to-I Human chr1 - 151004020 151004020 151004020 TACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCCGAGG TACTCGGGAGGCTGAGGCAGGAGAATCACTTGCACCCAGGAGGCAGAGGTTGCAGTGAGCCGAGG T G MINDY1 Ensembl:ENSG00000143409 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs986741417 Functional Loss SNV dbSNP153 33..33 33 - - - 36655 RMVar_ID_36655 Human_SNP_ID_33568538 A-to-I Human chr1 + 151073114 151073114 151073114 ATAGCTCATCGCATCCTTGAACTCCTGGGCTTAAGCTATCCTCCCGCCTTAGCCTCCTGAATAGC ATAGCTCATCGCATCCTTGAACTCCTGGGCTTCAGCTATCCTCCCGCCTTAGCCTCCTGAATAGC A C GABPB2 Ensembl:ENSG00000143458 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1484523159 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_128272,Human_Splice_Rec_128273 36656 RMVar_ID_36656 Human_SNP_ID_33568569 A-to-I Human chr1 + 151073211 151073211 151073211 TAATTTTTTTATTTTTGTATTTTTGTAGAGACAGAGTCCCTCTGTGTTGTCCCGGCTGGGATCAA TAATTTTTTTATTTTTGTATTTTTGTAGAGACGGAGTCCCTCTGTGTTGTCCCGGCTGGGATCAA A G GABPB2 Ensembl:ENSG00000143458 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474437058 Functional Loss SNV dbSNP153 33..33 33 - - - 36657 RMVar_ID_36657 Human_SNP_ID_33568802 A-to-I Human chr1 + 151074070 151074070 151074070 GCTATCTCGGCTCGCTGCAAGCTCCGCTTCCTAGTTCATGCCATTCTCCTGCCTCAGCCTCCTGA GCTATCTCGGCTCGCTGCAAGCTCCGCTTCCTGGTTCATGCCATTCTCCTGCCTCAGCCTCCTGA A G GABPB2 Ensembl:ENSG00000143458 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1250279579 Functional Loss SNV dbSNP153 33..33 33 - - - 36658 RMVar_ID_36658 Human_SNP_ID_33569141 A-to-I Human chr1 + 151075074 151075074 151075074 TGAGGCAGGAGAATTGCTTGAGCATTAGAGGCAGAGGTTGTGGCGAGCCGAGATCGTGCCACCGC TGAGGCAGGAGAATTGCTTGAGCATTAGAGGCCGAGGTTGTGGCGAGCCGAGATCGTGCCACCGC A C GABPB2 Ensembl:ENSG00000143458 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs952354456 Functional Loss SNV dbSNP153 33..33 33 - - - 36659 RMVar_ID_36659 Human_SNP_ID_33569343 A-to-I Human chr1 + 151075666 151075666 151075666 GGGAGGCGGAAGTTGCAGCGAGCTGAGACTGCACCACTGGACTCCAGCCTAGGCAACAGAGCGAG GGGAGGCGGAAGTTGCAGCGAGCTGAGACTGCGCCACTGGACTCCAGCCTAGGCAACAGAGCGAG A G GABPB2 Ensembl:ENSG00000143458 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1018178202 Functional Loss SNV dbSNP153 33..33 33 - - - 36660 RMVar_ID_36660 Human_SNP_ID_33571210 A-to-I Human chr1 + 151081796 151081796 151081796 AGCTGAGACTGCAGACGTGCACCACCATGCCCAGCTAATTCTTTTGTATTTTTTGAAAAGACAGA AGCTGAGACTGCAGACGTGCACCACCATGCCCCGCTAATTCTTTTGTATTTTTTGAAAAGACAGA A C GABPB2 Ensembl:ENSG00000143458 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1308548163 Functional Loss SNV dbSNP153 33..33 33 - - - 36661 RMVar_ID_36661 Human_SNP_ID_33571741 A-to-I Human chr1 + 151083523 151083523 151083523 GGACGTGGTGGCACATGCCTGTAATCCGAGCTACTCGGAAGGCTGAGGCAGAGAATTGCTTGAAC GGACGTGGTGGCACATGCCTGTAATCCGAGCTGCTCGGAAGGCTGAGGCAGAGAATTGCTTGAAC A G GABPB2 Ensembl:ENSG00000143458 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1200621871 Functional Loss SNV dbSNP153 33..33 33 - - - 36662 RMVar_ID_36662 Human_SNP_ID_33572671 A-to-I Human chr1 + 151086767 151086767 151086767 TCAGCTCACTGCAACCTCCACCTCCTGAGCTCAAGTTTTCCTCCCACTTTAGCCTCCTGAGTAGC TCAGCTCACTGCAACCTCCACCTCCTGAGCTCGAGTTTTCCTCCCACTTTAGCCTCCTGAGTAGC A G GABPB2 Ensembl:ENSG00000143458 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1038891355 Functional Loss SNV dbSNP153 33..33 33 - - - 36663 RMVar_ID_36663 Human_SNP_ID_33581029 A-to-I Human chr1 + 151119049 151119049 151119049 GAAACTGAAATAAGCTGCGTGTGGTGGCTCACACCTGTAATCCCAACACTTTGGGACGTTGAAAT GAAACTGAAATAAGCTGCGTGTGGTGGCTCACGCCTGTAATCCCAACACTTTGGGACGTTGAAAT A G GABPB2 Ensembl:ENSG00000143458 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1237223574 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17725451,Human_RBP_ID_26386397 36664 RMVar_ID_36664 Human_SNP_ID_33581054 A-to-I Human chr1 + 151119185 151119185 151119185 TAAAAATTAGCCAAGTATGGTGACAGGCACCTATGGTTCCAGCTACTCAGGAGGCTGAGGTGGGA TAAAAATTAGCCAAGTATGGTGACAGGCACCTGTGGTTCCAGCTACTCAGGAGGCTGAGGTGGGA A G GABPB2 Ensembl:ENSG00000143458 Protein coding 3'UTR GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1051621843 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26386398 36665 RMVar_ID_36665 Human_SNP_ID_33581069 A-to-I Human chr1 + 151119304 151119304 151119304 CTCTCCAGGCTTGAGTGACAGAGCAAGACTGTATCTCAAAGGAAAAAGGAAACTAGGCCAGGCGT CTCTCCAGGCTTGAGTGACAGAGCAAGACTGTTTCTCAAAGGAAAAAGGAAACTAGGCCAGGCGT A T GABPB2 Ensembl:ENSG00000143458 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1211491120 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5688796 36666 RMVar_ID_36666 Human_SNP_ID_33581076 A-to-I Human chr1 + 151119331 151119331 151119331 ACTGTATCTCAAAGGAAAAAGGAAACTAGGCCAGGCGTGGTGGCTCACGCCTGTAATCCCAACAC ACTGTATCTCAAAGGAAAAAGGAAACTAGGCCGGGCGTGGTGGCTCACGCCTGTAATCCCAACAC A G GABPB2 Ensembl:ENSG00000143458 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs182393479 Functional Loss SNV dbSNP153 33..33 33 - - - 36667 RMVar_ID_36667 Human_SNP_ID_33581087 A-to-I Human chr1 + 151119353 151119353 151119353 AAACTAGGCCAGGCGTGGTGGCTCACGCCTGTAATCCCAACACTTTGGGAGGCCGAGGCGGGCGG AAACTAGGCCAGGCGTGGTGGCTCACGCCTGTTATCCCAACACTTTGGGAGGCCGAGGCGGGCGG A T GABPB2 Ensembl:ENSG00000143458 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs985216109 Functional Loss SNV dbSNP153 33..33 33 - - - 36668 RMVar_ID_36668 Human_SNP_ID_33581089 A-to-I Human chr1 + 151119359 151119359 151119359 GGCCAGGCGTGGTGGCTCACGCCTGTAATCCCAACACTTTGGGAGGCCGAGGCGGGCGGATCACG GGCCAGGCGTGGTGGCTCACGCCTGTAATCCCGACACTTTGGGAGGCCGAGGCGGGCGGATCACG A G GABPB2 Ensembl:ENSG00000143458 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1182599415 Functional Loss SNV dbSNP153 33..33 33 - - - 36669 RMVar_ID_36669 Human_SNP_ID_33581295 A-to-I Human chr1 + 151120049 151120049 151120049 CCTGACCAACATGGAGAAACCCTGTCTCTACTAAAAATACAAAATTAGGGCCAGACCCGGCAGCT CCTGACCAACATGGAGAAACCCTGTCTCTACTGAAAATACAAAATTAGGGCCAGACCCGGCAGCT A G GABPB2 Ensembl:ENSG00000143458 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs979399772 Functional Loss SNV dbSNP153 33..33 33 - - - 36670 RMVar_ID_36670 Human_SNP_ID_33581326 A-to-I Human chr1 + 151120177 151120176 151120177 GACCAGCCTGGCCGAGATGGTGAAACCCTACTAAAAATACAAAAATTCACCTGGCGAGGTGGCAG GACCAGCCTGGCCGAGATGGTGAAACCCTACT_AAAATACAAAAATTCACCTGGCGAGGTGGCAG TA T GABPB2 Ensembl:ENSG00000143458 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs754039924 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_17725453 36671 RMVar_ID_36671 Human_SNP_ID_33581372 A-to-I Human chr1 + 151120389 151120389 151120389 AAAATTAGCTGGGTGTGGTGGCACATGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA AAAATTAGCTGGGTGTGGTGGCACATGCCTGTCATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA A C GABPB2 Ensembl:ENSG00000143458 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1252982515 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1355343 36672 RMVar_ID_36672 Human_SNP_ID_33581975 A-to-I Human chr1 + 151123231 151123231 151123231 TAATCCCAGCACTTTGAGAGGCTGAGGTGGGTAGATCACTTGAGGTGAGGAGTTCGAGACCAGCC TAATCCCAGCACTTTGAGAGGCTGAGGTGGGTGGATCACTTGAGGTGAGGAGTTCGAGACCAGCC A G GABPB2 Ensembl:ENSG00000143458 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs1173736024 Functional Loss SNV dbSNP153 33..33 33 - - - 36673 RMVar_ID_36673 Human_SNP_ID_33581996 A-to-I Human chr1 + 151123334 151123334 151123334 AAAATTAGTTGGGCATGATGGCATACGCCTGTAGTCCCAGCTACTCTGGAGGCTGAAACAGGAGA AAAATTAGTTGGGCATGATGGCATACGCCTGTGGTCCCAGCTACTCTGGAGGCTGAAACAGGAGA A G GABPB2 Ensembl:ENSG00000143458 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1558168538 Functional Loss SNV dbSNP153 33..33 33 - - - 36674 RMVar_ID_36674 Human_SNP_ID_33582047 A-to-I Human chr1 + 151123581 151123581 151123581 TCTACTTTAAAATAAAGCTGCTGGCCGGGCACAGTGGCTCACGCCTGTAACCTCAGCACTTTGGG TCTACTTTAAAATAAAGCTGCTGGCCGGGCACGGTGGCTCACGCCTGTAACCTCAGCACTTTGGG A G GABPB2 Ensembl:ENSG00000143458 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1167702763 Functional Loss SNV dbSNP153 33..33 33 - - - 36675 RMVar_ID_36675 Human_SNP_ID_33582074 A-to-I Human chr1 + 151123669 151123669 151123669 GGTCAGGAGATTGAGACCATCCTGGCTAACACAGTGAAACCCTGGCCCTACTAAAAATACAAAAA GGTCAGGAGATTGAGACCATCCTGGCTAACACGGTGAAACCCTGGCCCTACTAAAAATACAAAAA A G GABPB2 Ensembl:ENSG00000143458 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1372115328 Functional Loss SNV dbSNP153 33..33 33 - - - 36676 RMVar_ID_36676 Human_SNP_ID_33582114 A-to-I Human chr1 + 151123777 151123777 151123777 GGGAGGCTGAGGCAGGAGAATGACGTGAACCCAGGAGGCAGAGCTTGCAGTGAGCTGAGATCGCC GGGAGGCTGAGGCAGGAGAATGACGTGAACCCGGGAGGCAGAGCTTGCAGTGAGCTGAGATCGCC A G GABPB2 Ensembl:ENSG00000143458 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs1463938338 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23302808 36677 RMVar_ID_36677 Human_SNP_ID_33582314 A-to-I Human chr1 + 151124323 151124323 151124323 AGCTGGGATTACAGGCACGCGCTAATTTTTGTATTTTTAGTACAGACGGGATTTCACCATATTGG AGCTGGGATTACAGGCACGCGCTAATTTTTGTGTTTTTAGTACAGACGGGATTTCACCATATTGG A G GABPB2 Ensembl:ENSG00000143458 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs587677154 Functional Loss SNV dbSNP153 33..33 33 - - - 36678 RMVar_ID_36678 Human_SNP_ID_33582316 A-to-I Human chr1 + 151124329 151124329 151124329 GATTACAGGCACGCGCTAATTTTTGTATTTTTAGTACAGACGGGATTTCACCATATTGGCCAGGC GATTACAGGCACGCGCTAATTTTTGTATTTTTCGTACAGACGGGATTTCACCATATTGGCCAGGC A C GABPB2 Ensembl:ENSG00000143458 Protein coding 3'UTR GSE38233;GSE100210;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 24183664,29129909,30559470 RNA-Seq:(High) rs1332058346 Functional Loss SNV dbSNP153 33..33 33 - - - 36679 RMVar_ID_36679 Human_SNP_ID_33594110 A-to-I Human chr1 + 151167686 151167686 151167686 AAATCCTGTCTCTACCAAAAATGTAAAAAATTAGCTGGGTGTGTGGTGTGTGCCTGTAATCCCAG AAATCCTGTCTCTACCAAAAATGTAAAAAATTGGCTGGGTGTGTGGTGTGTGCCTGTAATCCCAG A G SCNM1 Ensembl:ENSG00000163156 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1238975237 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23332070 RMVar_hsa_circ_90462,RMVar_hsa_circ_136047 36680 RMVar_ID_36680 Human_SNP_ID_33599499 A-to-I Human chr1 - 151188954 151188954 151188954 GTGGTGGTGTGCGCCTATAGTCCCAGCTACTCAGGAGGCTGAGGCAGAGAATCGCTTGAACCTGG GTGGTGGTGTGCGCCTATAGTCCCAGCTACTCGGGAGGCTGAGGCAGAGAATCGCTTGAACCTGG T C VPS72 Ensembl:ENSG00000163159 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs375508532 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119046,RMVar_hsa_circ_136056 36681 RMVar_ID_36681 Human_SNP_ID_33600897 A-to-I Human chr1 - 151194552 151194552 151194552 AATACAAAAATTCGCTGAGCGTGGTGGTGCGCACCTGTAGTCACAGCTACTAAGGAAACTGAGAT AATACAAAAATTCGCTGAGCGTGGTGGTGCGCGCCTGTAGTCACAGCTACTAAGGAAACTGAGAT T C VPS72 Ensembl:ENSG00000163159 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941050390 Functional Loss SNV dbSNP153 33..33 33 - - - 36682 RMVar_ID_36682 Human_SNP_ID_33600898 A-to-I Human chr1 - 151194552 151194552 151194552 AATACAAAAATTCGCTGAGCGTGGTGGTGCGCACCTGTAGTCACAGCTACTAAGGAAACTGAGAT AATACAAAAATTCGCTGAGCGTGGTGGTGCGCCCCTGTAGTCACAGCTACTAAGGAAACTGAGAT T G VPS72 Ensembl:ENSG00000163159 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941050390 Functional Loss SNV dbSNP153 33..33 33 - - - 36683 RMVar_ID_36683 Human_SNP_ID_33600917 A-to-I Human chr1 - 151194596 151194596 151194596 AAGACTAGCCTGGGCAACATGGCAAAAATCCTATCTCTACAAAAAATACAAAAATTCGCTGAGCG AAGACTAGCCTGGGCAACATGGCAAAAATCCTGTCTCTACAAAAAATACAAAAATTCGCTGAGCG T C VPS72 Ensembl:ENSG00000163159 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1022173824 Functional Loss SNV dbSNP153 33..33 33 - - - 36684 RMVar_ID_36684 Human_SNP_ID_33600918 A-to-I Human chr1 - 151194603 151194600 151194603 GGGGTTCAAGACTAGCCTGGGCAACATGGCAAAAATCCTATCTCTACAAAAAATACAAAAATTCG GGGGTTCAAGACTAGCCTGGGCAACATGGCAA___TCCTATCTCTACAAAAAATACAAAAATTCG ATTT A VPS72 Ensembl:ENSG00000163159 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs368423675 Functional Loss DEL dbSNP153 33..35 33 - - - 36685 RMVar_ID_36685 Human_SNP_ID_33602349 A-to-I Human chr1 + 151199451 151199451 151199451 CCTGGCCAACATAGAGAAATCTCGTCCCTACTAAAAATACAAAAATTATCCGGACAGTAGTGGCG CCTGGCCAACATAGAGAAATCTCGTCCCTACTGAAAATACAAAAATTATCCGGACAGTAGTGGCG A G PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285202779 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11183284 36686 RMVar_ID_36686 Human_SNP_ID_33602366 A-to-I Human chr1 + 151199520 151199520 151199520 TCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGATAATCCCTTGAGCCTGGGAGGCAGAGCTT TCTGTAATCCCAGCTACTTGGGAGGCTGAGGCGGGATAATCCCTTGAGCCTGGGAGGCAGAGCTT A G PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1184919991 Functional Loss SNV dbSNP153 33..33 33 - - - 36687 RMVar_ID_36687 Human_SNP_ID_33602809 A-to-I Human chr1 + 151201095 151201095 151201095 TGACCCTGTGATCCGCCCGCCTTGGCTTCCCAAAGTGCTGGGATTATAGGCGTGAGCCACCGTGC TGACCCTGTGATCCGCCCGCCTTGGCTTCCCAGAGTGCTGGGATTATAGGCGTGAGCCACCGTGC A G PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs587623147 Functional Loss SNV dbSNP153 33..33 33 - - - 36688 RMVar_ID_36688 Human_SNP_ID_33602873 A-to-I Human chr1 + 151201378 151201378 151201378 ATGTTTTTGTGGTTTTTTTTTTGAGACAGAGTATCATTCTGTCACCCAGGCTGGAGTGCAGTGGT ATGTTTTTGTGGTTTTTTTTTTGAGACAGAGTCTCATTCTGTCACCCAGGCTGGAGTGCAGTGGT A C PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1445566736 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3281161,Human_RBP_ID_22708011 36689 RMVar_ID_36689 Human_SNP_ID_33602876 A-to-I Human chr1 + 151201389 151201389 151201389 GTTTTTTTTTTGAGACAGAGTATCATTCTGTCACCCAGGCTGGAGTGCAGTGGTGCCATCTTGGC GTTTTTTTTTTGAGACAGAGTATCATTCTGTCGCCCAGGCTGGAGTGCAGTGGTGCCATCTTGGC A G PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1240814955 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22708011 36690 RMVar_ID_36690 Human_SNP_ID_33602916 A-to-I Human chr1 + 151201570 151201570 151201570 TAGTGATGGGGTTTCATCATGTCAGCCAGACTAGTCTTGAACTCCTGACCTCAAGTAATCCGCCC TAGTGATGGGGTTTCATCATGTCAGCCAGACTGGTCTTGAACTCCTGACCTCAAGTAATCCGCCC A G PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1429430606 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10576540,Human_RBP_ID_17557311 36691 RMVar_ID_36691 Human_SNP_ID_33602944 A-to-I Human chr1 + 151201672 151201672 151201672 CGCAAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAAATA CGCAAGGTCAGGAGTTCGAGACCAGCCTGGCCCACATGGTGAAACCCCATCTCTACTAAAAAATA A C PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs12733535 Functional Loss SNV dbSNP153 33..33 33 - - - 36692 RMVar_ID_36692 Human_SNP_ID_33602945 A-to-I Human chr1 + 151201672 151201672 151201672 CGCAAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAAATA CGCAAGGTCAGGAGTTCGAGACCAGCCTGGCCGACATGGTGAAACCCCATCTCTACTAAAAAATA A G PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs12733535 Functional Loss SNV dbSNP153 33..33 33 - - - 36693 RMVar_ID_36693 Human_SNP_ID_33602968 A-to-I Human chr1 + 151201751 151201751 151201751 AGGCATGTTGGCGCAGGCCTGTAATCCCAGCTACTTAGGAGGCTGAGTCAGGAGAATTGCTTGAA AGGCATGTTGGCGCAGGCCTGTAATCCCAGCTGCTTAGGAGGCTGAGTCAGGAGAATTGCTTGAA A G PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1454389654 Functional Loss SNV dbSNP153 33..33 33 - - - 36694 RMVar_ID_36694 Human_SNP_ID_33603189 A-to-I Human chr1 + 151202635 151202635 151202635 CAGATTACAGGCACCTGCCACCACATCTGACTAATTTTTGTATTTTAGTAGAGACAGGGTTTCAC CAGATTACAGGCACCTGCCACCACATCTGACTGATTTTTGTATTTTAGTAGAGACAGGGTTTCAC A G PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1200041146 Functional Loss SNV dbSNP153 33..33 33 - - - 36695 RMVar_ID_36695 Human_SNP_ID_33603265 A-to-I Human chr1 + 151202898 151202898 151202898 GAGTTCAAGCGATTCTCCTGCTTCAGCTTCCCAAGTAACTGAGATTACAGGCACCTGCCACGTCT GAGTTCAAGCGATTCTCCTGCTTCAGCTTCCCGAGTAACTGAGATTACAGGCACCTGCCACGTCT A G PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs868241496 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10576597 36696 RMVar_ID_36696 Human_SNP_ID_33603277 A-to-I Human chr1 + 151202952 151202952 151202952 CTGCCACGTCTGGCTAATTTTTGTATTTTAGTAGAGATCAGATTTCACCATGTTAGTCAGGCTGG CTGCCACGTCTGGCTAATTTTTGTATTTTAGTGGAGATCAGATTTCACCATGTTAGTCAGGCTGG A G PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1217019323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10576598,Human_RBP_ID_27388026 36697 RMVar_ID_36697 Human_SNP_ID_33603285 A-to-I Human chr1 + 151202974 151202974 151202974 GTATTTTAGTAGAGATCAGATTTCACCATGTTAGTCAGGCTGGTCTCAAACTCCTGACCTCAGGT GTATTTTAGTAGAGATCAGATTTCACCATGTTGGTCAGGCTGGTCTCAAACTCCTGACCTCAGGT A G PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1283644223 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10576598 36698 RMVar_ID_36698 Human_SNP_ID_33603361 A-to-I Human chr1 + 151203271 151203271 151203271 GCACTTGAGGCTGGGTACAATGGCTCACACCTATATTCTCAGCACTTTGGGAGGCCAAGGCAGGC GCACTTGAGGCTGGGTACAATGGCTCACACCTGTATTCTCAGCACTTTGGGAGGCCAAGGCAGGC A G PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971665496 Functional Loss SNV dbSNP153 33..33 33 - - - 36699 RMVar_ID_36699 Human_SNP_ID_33603407 A-to-I Human chr1 + 151203470 151203469 151203470 AGAATTGCTTGAACCCGGGGGACAGAGGTTGCAATGAGTCAAGATCACACCATTGCATTCCAGCC AGAATTGCTTGAACCCGGGGGACAGAGGTTGC_ATGAGTCAAGATCACACCATTGCATTCCAGCC CA C PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1002604851 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_22708012,Human_RBP_ID_24586480 36700 RMVar_ID_36700 Human_SNP_ID_33603408 A-to-I Human chr1 + 151203470 151203470 151203470 AGAATTGCTTGAACCCGGGGGACAGAGGTTGCAATGAGTCAAGATCACACCATTGCATTCCAGCC AGAATTGCTTGAACCCGGGGGACAGAGGTTGCCATGAGTCAAGATCACACCATTGCATTCCAGCC A C PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1054562121 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22708012,Human_RBP_ID_24586480 36701 RMVar_ID_36701 Human_SNP_ID_33603453 A-to-I Human chr1 + 151203633 151203633 151203633 GGATCACAAGCTCAAGAGATGGAGACCATCCTAACCAACGTGGTGAAACCCCGTCTCTACTAAAA GGATCACAAGCTCAAGAGATGGAGACCATCCTGACCAACGTGGTGAAACCCCGTCTCTACTAAAA A G PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1558232800 Functional Loss SNV dbSNP153 33..33 33 - - - 36702 RMVar_ID_36702 Human_SNP_ID_33603675 A-to-I Human chr1 + 151204342 151204342 151204342 GGGATTACAGGCACCCGCCAACACGCCCGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCG GGGATTACAGGCACCCGCCAACACGCCCGGCTCATTTTTGTATTTTTAGTAGAGACGGGGTTTCG A C PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1211153928 Functional Loss SNV dbSNP153 33..33 33 - - - 36703 RMVar_ID_36703 Human_SNP_ID_33603871 A-to-I Human chr1 + 151205255 151205255 151205255 TGTAGTGCAGTGGTGCGATCTTGGCTCACTGCAGCCCTTGCCTCCCAGGTTCAAGCGATTCTCCT TGTAGTGCAGTGGTGCGATCTTGGCTCACTGCCGCCCTTGCCTCCCAGGTTCAAGCGATTCTCCT A C PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1027720798 Functional Loss SNV dbSNP153 33..33 33 - - - 36704 RMVar_ID_36704 Human_SNP_ID_33603883 A-to-I Human chr1 + 151205309 151205309 151205309 GCGATTCTCCTGCCTCAGCCTCCTAGGTCACTAGGATCACAGGCGTGCGCCACCACGCCCAGATA GCGATTCTCCTGCCTCAGCCTCCTAGGTCACTCGGATCACAGGCGTGCGCCACCACGCCCAGATA A C PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs952675866 Functional Loss SNV dbSNP153 33..33 33 - - - 36705 RMVar_ID_36705 Human_SNP_ID_33603924 A-to-I Human chr1 + 151205436 151205436 151205436 GGCCTCAAGCGATCCTCCTGCCTTGGCTTCCCAAAGTTCTGAGATTACAGGCGTGAGCTACTGCC GGCCTCAAGCGATCCTCCTGCCTTGGCTTCCCCAAGTTCTGAGATTACAGGCGTGAGCTACTGCC A C PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1056958839 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557313,Human_RBP_ID_23144099 36706 RMVar_ID_36706 Human_SNP_ID_33604627 A-to-I Human chr1 + 151208059 151208059 151208059 TTTTGTATTTTTAGTAGAAATGGGGTTTCTCCATGTTGGGTCAGGCTGTTCTCGAACTCCTAACT TTTTGTATTTTTAGTAGAAATGGGGTTTCTCCGTGTTGGGTCAGGCTGTTCTCGAACTCCTAACT A G PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs587705040 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5689076,Human_RBP_ID_10576833 36707 RMVar_ID_36707 Human_SNP_ID_33604637 A-to-I Human chr1 + 151208103 151208103 151208103 GCTGTTCTCGAACTCCTAACTTCAGCTGATCCACCTGCCTTGGCCTCCCAAAGTGCTGGGATTAC GCTGTTCTCGAACTCCTAACTTCAGCTGATCCGCCTGCCTTGGCCTCCCAAAGTGCTGGGATTAC A G PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277313625 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10576833 36708 RMVar_ID_36708 Human_SNP_ID_33605473 A-to-I Human chr1 + 151210787 151210787 151210787 TTTTTGTATTTTTAGTAGAGACGGGTTTTGCCATGTTGACCAGGCTGGTTTTGATCTCCTGACCT TTTTTGTATTTTTAGTAGAGACGGGTTTTGCCGTGTTGACCAGGCTGGTTTTGATCTCCTGACCT A G PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1224793905 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5125739,Human_RBP_ID_10576980,Human_RBP_ID_24586628 36709 RMVar_ID_36709 Human_SNP_ID_33605606 A-to-I Human chr1 + 151211405 151211405 151211405 GCTACTCTGGAGTCTGAGGGGAGAATCACTTGAACCTGAGAGGTTGAGGCTGCAGTAAGCTGTGT GCTACTCTGGAGTCTGAGGGGAGAATCACTTGGACCTGAGAGGTTGAGGCTGCAGTAAGCTGTGT A G PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232606307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10577011,Human_RBP_ID_17557315,Human_RBP_ID_22470144 36710 RMVar_ID_36710 Human_SNP_ID_33605815 A-to-I Human chr1 + 151211965 151211965 151211965 CTCTACTAAAAACAAAAAATAAAAAAAAAATTAGCTGGGTGTGGTGGCAGGTGCCTGTAGTCCTA CTCTACTAAAAACAAAAAATAAAAAAAAAATTCGCTGGGTGTGGTGGCAGGTGCCTGTAGTCCTA A C PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1558246039 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_101511,Human_RBP_ID_24586654 36711 RMVar_ID_36711 Human_SNP_ID_33606011 A-to-I Human chr1 + 151212628 151212628 151212628 GACGGAGTCTCGCTCTGTCGCCAGGCTGGAGTACAGTGGCATGATCTCTGCTTACTGCAATCTCT GACGGAGTCTCGCTCTGTCGCCAGGCTGGAGTGCAGTGGCATGATCTCTGCTTACTGCAATCTCT A G PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215518296 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10577059,Human_RBP_ID_19190494 36712 RMVar_ID_36712 Human_SNP_ID_33606858 A-to-I Human chr1 + 151215435 151215435 151215435 TCACTTCCAGCTCTGCCTCCTGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGAGAAGCTGGGA TCACTTCCAGCTCTGCCTCCTGGGTTCAAGCGGTTCTCCTGCCTCAGCCTCCTGAGAAGCTGGGA A G PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs587646544 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24586721 36713 RMVar_ID_36713 Human_SNP_ID_33606859 A-to-I Human chr1 + 151215435 151215435 151215435 TCACTTCCAGCTCTGCCTCCTGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGAGAAGCTGGGA TCACTTCCAGCTCTGCCTCCTGGGTTCAAGCGTTTCTCCTGCCTCAGCCTCCTGAGAAGCTGGGA A T PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs587646544 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24586721 36714 RMVar_ID_36714 Human_SNP_ID_33606885 A-to-I Human chr1 + 151215530 151215530 151215530 TTTTGTATTTTTAGTAGAGACGGGTTTTCACCATGTTGGCCAGGAGGCTGGTCTTGTGAACTCTT TTTTGTATTTTTAGTAGAGACGGGTTTTCACCGTGTTGGCCAGGAGGCTGGTCTTGTGAACTCTT A G PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1172668223 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10577181 36715 RMVar_ID_36715 Human_SNP_ID_33607396 A-to-I Human chr1 + 151217102 151217102 151217102 ACCCAGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTTTCCACGTTGGCCAGGCTGGTCTTGA ACCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTTTCCACGTTGGCCAGGCTGGTCTTGA A G PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1245293150 Functional Loss SNV dbSNP153 33..33 33 - - - 36716 RMVar_ID_36716 Human_SNP_ID_33607415 A-to-I Human chr1 + 151217173 151217173 151217173 GGCCTCAAGTGACCCACCCACTAGGCCTCCCAAAGTGCTGGGATTACAGGCTTGAGCCATTGTGC GGCCTCAAGTGACCCACCCACTAGGCCTCCCAGAGTGCTGGGATTACAGGCTTGAGCCATTGTGC A G PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs778373016 Functional Loss SNV dbSNP153 33..33 33 - - - 36717 RMVar_ID_36717 Human_SNP_ID_33607509 A-to-I Human chr1 + 151217694 151217694 151217694 GCACTGACCTCCCAGGCCCAGGCCATCTTCCCACCTCAGCCTCACAAGTAGCTGGGACTACAGAC GCACTGACCTCCCAGGCCCAGGCCATCTTCCCGCCTCAGCCTCACAAGTAGCTGGGACTACAGAC A G PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968153372 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11183430,Human_RBP_ID_24586753 36718 RMVar_ID_36718 Human_SNP_ID_33607694 A-to-I Human chr1 + 151218581 151218581 151218581 AGATGAGGCCGGGCTCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGTGGA AGATGAGGCCGGGCTCAGTGGCTCACGCCTGTGATCCCAGCACTTTGGGAGGCCAAGGCAGTGGA A G PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1312876864 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10577366,Human_RBP_ID_24586769 36719 RMVar_ID_36719 Human_SNP_ID_33607840 A-to-I Human chr1 + 151219123 151219123 151219123 GGAAAGTAGGCTGGGCACAATGGCTCACGCCTATAATCCCAGCACTTTGGAAGGATGAGGTGGGC GGAAAGTAGGCTGGGCACAATGGCTCACGCCTGTAATCCCAGCACTTTGGAAGGATGAGGTGGGC A G PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1314504218 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557316 36720 RMVar_ID_36720 Human_SNP_ID_33607852 A-to-I Human chr1 + 151219194 151219194 151219194 CTTGAGGTCAGGAGTTCCAGACCAGGCTGGCCAACATGGCGAAACCCTGTCTGTACTAAAAATAC CTTGAGGTCAGGAGTTCCAGACCAGGCTGGCCCACATGGCGAAACCCTGTCTGTACTAAAAATAC A C PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1418960278 Functional Loss SNV dbSNP153 33..33 33 - - - 36721 RMVar_ID_36721 Human_SNP_ID_33607967 A-to-I Human chr1 + 151219547 151219547 151219547 CATCTCTACAAAAAATTTAAAAAAAAAAAATTAGCTGGGTGTTGTGGTGCGTGCCTGTAATCCCA CATCTCTACAAAAAATTTAAAAAAAAAAAATTGGCTGGGTGTTGTGGTGCGTGCCTGTAATCCCA A G PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1293287332 Functional Loss SNV dbSNP153 33..33 33 - - - 36722 RMVar_ID_36722 Human_SNP_ID_33607978 A-to-I Human chr1 + 151219573 151219573 151219573 AAAATTAGCTGGGTGTTGTGGTGCGTGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTAGCTGGGTGTTGTGGTGCGTGCCTGTTATCCCAGCTACTCGGGAGGCTGAGGCAGGAGA A T PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1002620383 Functional Loss SNV dbSNP153 33..33 33 - - - 36723 RMVar_ID_36723 Human_SNP_ID_33608177 A-to-I Human chr1 + 151220075 151220075 151220075 TTGCCCAGGCTGGAGTGCAGTGGCGCGATCTCAGCTCACTGCAATCTCTGTCTCCCAGGTTCAAG TTGCCCAGGCTGGAGTGCAGTGGCGCGATCTCGGCTCACTGCAATCTCTGTCTCCCAGGTTCAAG A G PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1558260779 Functional Loss SNV dbSNP153 33..33 33 - - - 36724 RMVar_ID_36724 Human_SNP_ID_33608283 A-to-I Human chr1 + 151220486 151220486 151220486 CCATATACTTACCACCTAGCTTTTTTTTTTTTAAGACAGGATTTCACTCTTTCGCCCAGGCAGGA CCATATACTTACCACCTAGCTTTTTTTTTTTTTAGACAGGATTTCACTCTTTCGCCCAGGCAGGA A T PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1181908793 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5689175,Human_RBP_ID_10577422,Human_RBP_ID_17557319,Human_RBP_ID_23144203 36725 RMVar_ID_36725 Human_SNP_ID_33608310 A-to-I Human chr1 + 151220567 151220567 151220567 TCAGCTTACTGCAACCTCTGCTCCCCGGGTTCAACCGATTCTCCTGCCTCAGCCTCCAAGTATTT TCAGCTTACTGCAACCTCTGCTCCCCGGGTTCGACCGATTCTCCTGCCTCAGCCTCCAAGTATTT A G PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-Seq:(High) rs587700813 Functional Loss SNV dbSNP153 33..33 33 - - - 36726 RMVar_ID_36726 Human_SNP_ID_33608320 A-to-I Human chr1 + 151220608 151220608 151220608 TCCTGCCTCAGCCTCCAAGTATTTGGGATTACAGGCGCCCACCACCTTGCCCAGCTAATTTTTGT TCCTGCCTCAGCCTCCAAGTATTTGGGATTACGGGCGCCCACCACCTTGCCCAGCTAATTTTTGT A G PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs984041578 Functional Loss SNV dbSNP153 33..33 33 - - - 36727 RMVar_ID_36727 Human_SNP_ID_33608327 A-to-I Human chr1 + 151220647 151220647 151220647 CACCACCTTGCCCAGCTAATTTTTGTGTTTTTAGTAGAGATGGGGTTTCGCCATGTTGGCAAGGC CACCACCTTGCCCAGCTAATTTTTGTGTTTTTTGTAGAGATGGGGTTTCGCCATGTTGGCAAGGC A T PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1363858587 Functional Loss SNV dbSNP153 33..33 33 - - - 36728 RMVar_ID_36728 Human_SNP_ID_33608329 A-to-I Human chr1 + 151220650 151220650 151220650 CACCTTGCCCAGCTAATTTTTGTGTTTTTAGTAGAGATGGGGTTTCGCCATGTTGGCAAGGCTGG CACCTTGCCCAGCTAATTTTTGTGTTTTTAGTGGAGATGGGGTTTCGCCATGTTGGCAAGGCTGG A G PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1436473417 Functional Loss SNV dbSNP153 33..33 33 - - - 36729 RMVar_ID_36729 Human_SNP_ID_33608350 A-to-I Human chr1 + 151220727 151220727 151220727 GACCTCACGTGATCCACCTGCCTTGGCCTTCCAAAGTGCTGGGATTACAGGCGTGAGCCACTTTA GACCTCACGTGATCCACCTGCCTTGGCCTTCCGAAGTGCTGGGATTACAGGCGTGAGCCACTTTA A G PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982047525 Functional Loss SNV dbSNP153 33..33 33 - - - 36730 RMVar_ID_36730 Human_SNP_ID_33608916 A-to-I Human chr1 + 151223174 151223174 151223174 GGAATTCAAGACCACCCTGGCCGACATGATGAAACCCCATCTCTGCTAAAAATACAAAAATCAGC GGAATTCAAGACCACCCTGGCCGACATGATGACACCCCATCTCTGCTAAAAATACAAAAATCAGC A C PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs763976300 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2093833 36731 RMVar_ID_36731 Human_SNP_ID_33609612 A-to-I Human chr1 + 151225650 151225650 151225650 CGCCACCATGCCCGCCTAATTTTTGTATTTTTAGTAGAGGCAGGGTTTCACCCTGTTGACCAGAC CGCCACCATGCCCGCCTAATTTTTGTATTTTTGGTAGAGGCAGGGTTTCACCCTGTTGACCAGAC A G PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1248135936 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5125280,Human_RBP_ID_10577651,Human_RBP_ID_22469465 RMVar_hsa_circ_136062,RMVar_hsa_circ_94058,RMVar_hsa_circ_308976,RMVar_hsa_circ_350364,RMVar_hsa_circ_336742,RMVar_hsa_circ_293693,RMVar_hsa_circ_303523,RMVar_hsa_circ_277260,RMVar_hsa_circ_136064,RMVar_hsa_circ_136065,RMVar_hsa_circ_136066,RMVar_hsa_circ_136063,RMVar_hsa_circ_136068,RMVar_hsa_circ_271935,RMVar_hsa_circ_307083,RMVar_hsa_circ_370410,RMVar_hsa_circ_136061,RMVar_hsa_circ_334967,RMVar_hsa_circ_295327,RMVar_hsa_circ_136070,RMVar_hsa_circ_136071,RMVar_hsa_circ_136069,RMVar_hsa_circ_136067 36732 RMVar_ID_36732 Human_SNP_ID_33609614 A-to-I Human chr1 + 151225653 151225653 151225653 CACCATGCCCGCCTAATTTTTGTATTTTTAGTAGAGGCAGGGTTTCACCCTGTTGACCAGACTGG CACCATGCCCGCCTAATTTTTGTATTTTTAGTGGAGGCAGGGTTTCACCCTGTTGACCAGACTGG A G PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1292378452 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5125280,Human_RBP_ID_10577651,Human_RBP_ID_22469465 RMVar_hsa_circ_136062,RMVar_hsa_circ_94058,RMVar_hsa_circ_308976,RMVar_hsa_circ_350364,RMVar_hsa_circ_336742,RMVar_hsa_circ_293693,RMVar_hsa_circ_303523,RMVar_hsa_circ_277260,RMVar_hsa_circ_136064,RMVar_hsa_circ_136065,RMVar_hsa_circ_136066,RMVar_hsa_circ_136063,RMVar_hsa_circ_136068,RMVar_hsa_circ_271935,RMVar_hsa_circ_307083,RMVar_hsa_circ_370410,RMVar_hsa_circ_136061,RMVar_hsa_circ_334967,RMVar_hsa_circ_295327,RMVar_hsa_circ_136070,RMVar_hsa_circ_136071,RMVar_hsa_circ_136069,RMVar_hsa_circ_136067 36733 RMVar_ID_36733 Human_SNP_ID_33609782 A-to-I Human chr1 + 151226284 151226284 151226284 AATTTTTGTGTTTTTAGTAGAGACAGGGTTTCAACATCTTGGCCAGGCTGGTCTTGAACTCCTGA AATTTTTGTGTTTTTAGTAGAGACAGGGTTTCGACATCTTGGCCAGGCTGGTCTTGAACTCCTGA A G PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1053961286 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136062,RMVar_hsa_circ_94058,RMVar_hsa_circ_308976,RMVar_hsa_circ_350364,RMVar_hsa_circ_336742,RMVar_hsa_circ_293693,RMVar_hsa_circ_303523,RMVar_hsa_circ_277260,RMVar_hsa_circ_136064,RMVar_hsa_circ_136065,RMVar_hsa_circ_136066,RMVar_hsa_circ_136063,RMVar_hsa_circ_136068,RMVar_hsa_circ_271935,RMVar_hsa_circ_307083,RMVar_hsa_circ_370410,RMVar_hsa_circ_136061,RMVar_hsa_circ_334967,RMVar_hsa_circ_295327,RMVar_hsa_circ_136070,RMVar_hsa_circ_136071,RMVar_hsa_circ_136069,RMVar_hsa_circ_136067 36734 RMVar_ID_36734 Human_SNP_ID_33609800 A-to-I Human chr1 + 151226353 151226353 151226353 GTGATCCACTTGCCTCCACCTCCCAAAGTGCTAGTATTACAGGTGTGAGCCACCGCACCCGGCCA GTGATCCACTTGCCTCCACCTCCCAAAGTGCTGGTATTACAGGTGTGAGCCACCGCACCCGGCCA A G PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs752619486 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5125283,Human_RBP_ID_17557320,Human_RBP_ID_22469467,Human_RBP_ID_23144219 RMVar_hsa_circ_136062,RMVar_hsa_circ_94058,RMVar_hsa_circ_308976,RMVar_hsa_circ_350364,RMVar_hsa_circ_336742,RMVar_hsa_circ_293693,RMVar_hsa_circ_303523,RMVar_hsa_circ_277260,RMVar_hsa_circ_136064,RMVar_hsa_circ_136065,RMVar_hsa_circ_136066,RMVar_hsa_circ_136063,RMVar_hsa_circ_136068,RMVar_hsa_circ_271935,RMVar_hsa_circ_307083,RMVar_hsa_circ_370410,RMVar_hsa_circ_136061,RMVar_hsa_circ_334967,RMVar_hsa_circ_295327,RMVar_hsa_circ_136070,RMVar_hsa_circ_136071,RMVar_hsa_circ_136069,RMVar_hsa_circ_136067 36735 RMVar_ID_36735 Human_SNP_ID_33609801 A-to-I Human chr1 + 151226353 151226353 151226353 GTGATCCACTTGCCTCCACCTCCCAAAGTGCTAGTATTACAGGTGTGAGCCACCGCACCCGGCCA GTGATCCACTTGCCTCCACCTCCCAAAGTGCTTGTATTACAGGTGTGAGCCACCGCACCCGGCCA A T PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs752619486 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5125283,Human_RBP_ID_17557320,Human_RBP_ID_22469467,Human_RBP_ID_23144219 RMVar_hsa_circ_136062,RMVar_hsa_circ_94058,RMVar_hsa_circ_308976,RMVar_hsa_circ_350364,RMVar_hsa_circ_336742,RMVar_hsa_circ_293693,RMVar_hsa_circ_303523,RMVar_hsa_circ_277260,RMVar_hsa_circ_136064,RMVar_hsa_circ_136065,RMVar_hsa_circ_136066,RMVar_hsa_circ_136063,RMVar_hsa_circ_136068,RMVar_hsa_circ_271935,RMVar_hsa_circ_307083,RMVar_hsa_circ_370410,RMVar_hsa_circ_136061,RMVar_hsa_circ_334967,RMVar_hsa_circ_295327,RMVar_hsa_circ_136070,RMVar_hsa_circ_136071,RMVar_hsa_circ_136069,RMVar_hsa_circ_136067 36736 RMVar_ID_36736 Human_SNP_ID_33610807 A-to-I Human chr1 + 151230037 151230037 151230037 GTCAACCAGGGAGGCGGAGCTTGCAGTGAGCCAAGATCACGCCACTGCACTCCAGCCTGGGCGAC GTCAACCAGGGAGGCGGAGCTTGCAGTGAGCCGAGATCACGCCACTGCACTCCAGCCTGGGCGAC A G PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1400457939 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24751912 RMVar_hsa_circ_136062,RMVar_hsa_circ_94058,RMVar_hsa_circ_308976,RMVar_hsa_circ_350364,RMVar_hsa_circ_293693,RMVar_hsa_circ_303523,RMVar_hsa_circ_277260,RMVar_hsa_circ_136064,RMVar_hsa_circ_136065,RMVar_hsa_circ_136063,RMVar_hsa_circ_136068,RMVar_hsa_circ_271935,RMVar_hsa_circ_370410,RMVar_hsa_circ_136061,RMVar_hsa_circ_334967,RMVar_hsa_circ_295327,RMVar_hsa_circ_136070,RMVar_hsa_circ_136071,RMVar_hsa_circ_136069,RMVar_hsa_circ_101176,RMVar_hsa_circ_299595,RMVar_hsa_circ_285554,RMVar_hsa_circ_136073,RMVar_hsa_circ_136075,RMVar_hsa_circ_92230,RMVar_hsa_circ_136074,RMVar_hsa_circ_136072 36737 RMVar_ID_36737 Human_SNP_ID_33610938 A-to-I Human chr1 + 151230563 151230563 151230563 GCTCTTTTACCACACTGTTGCCCTTTTTTTTGAGACAGTCTGGCTGTGTTACCCAGGCTGGAATG GCTCTTTTACCACACTGTTGCCCTTTTTTTTGCGACAGTCTGGCTGTGTTACCCAGGCTGGAATG A C PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1298609438 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136062,RMVar_hsa_circ_94058,RMVar_hsa_circ_308976,RMVar_hsa_circ_350364,RMVar_hsa_circ_293693,RMVar_hsa_circ_303523,RMVar_hsa_circ_277260,RMVar_hsa_circ_136064,RMVar_hsa_circ_136065,RMVar_hsa_circ_136063,RMVar_hsa_circ_136068,RMVar_hsa_circ_271935,RMVar_hsa_circ_370410,RMVar_hsa_circ_136061,RMVar_hsa_circ_334967,RMVar_hsa_circ_295327,RMVar_hsa_circ_136070,RMVar_hsa_circ_136071,RMVar_hsa_circ_136069,RMVar_hsa_circ_101176,RMVar_hsa_circ_299595,RMVar_hsa_circ_285554,RMVar_hsa_circ_136073,RMVar_hsa_circ_136075,RMVar_hsa_circ_92230,RMVar_hsa_circ_136074,RMVar_hsa_circ_136072 36738 RMVar_ID_36738 Human_SNP_ID_33611051 A-to-I Human chr1 + 151231024 151231024 151231024 GGTTAGGAGCTTGAGACCAGCCTGACCAACATAGTGAAACCCCATCTGTACTAAAAATATAAAGA GGTTAGGAGCTTGAGACCAGCCTGACCAACATTGTGAAACCCCATCTGTACTAAAAATATAAAGA A T PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs587775240 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136062,RMVar_hsa_circ_94058,RMVar_hsa_circ_308976,RMVar_hsa_circ_350364,RMVar_hsa_circ_293693,RMVar_hsa_circ_303523,RMVar_hsa_circ_277260,RMVar_hsa_circ_136064,RMVar_hsa_circ_136065,RMVar_hsa_circ_136063,RMVar_hsa_circ_136068,RMVar_hsa_circ_271935,RMVar_hsa_circ_370410,RMVar_hsa_circ_136061,RMVar_hsa_circ_334967,RMVar_hsa_circ_295327,RMVar_hsa_circ_136070,RMVar_hsa_circ_136071,RMVar_hsa_circ_136069,RMVar_hsa_circ_101176,RMVar_hsa_circ_299595,RMVar_hsa_circ_285554,RMVar_hsa_circ_136073,RMVar_hsa_circ_136075,RMVar_hsa_circ_92230,RMVar_hsa_circ_136074,RMVar_hsa_circ_136072 36739 RMVar_ID_36739 Human_SNP_ID_33611687 A-to-I Human chr1 + 151233263 151233263 151233263 CTCCCACCTCAGCCTCTCACGTAGTTGGGACTAAAGGCACGCACCACCACACCTGGCTAATTTTT CTCCCACCTCAGCCTCTCACGTAGTTGGGACTGAAGGCACGCACCACCACACCTGGCTAATTTTT A G PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1304900520 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136062,RMVar_hsa_circ_94058,RMVar_hsa_circ_308976,RMVar_hsa_circ_293693,RMVar_hsa_circ_303523,RMVar_hsa_circ_136063,RMVar_hsa_circ_63943,RMVar_hsa_circ_370410,RMVar_hsa_circ_136061,RMVar_hsa_circ_334967,RMVar_hsa_circ_295327,RMVar_hsa_circ_136070,RMVar_hsa_circ_136071,RMVar_hsa_circ_136069,RMVar_hsa_circ_285554,RMVar_hsa_circ_136073,RMVar_hsa_circ_92230,RMVar_hsa_circ_136072,RMVar_hsa_circ_10979 36740 RMVar_ID_36740 Human_SNP_ID_33611713 A-to-I Human chr1 + 151233367 151233367 151233367 GCTTTGTTGTCCAAGCTGGAGTACAGTTGCACAATCTCGGCTCACTGCAACCTCCGCCTCCCAGG GCTTTGTTGTCCAAGCTGGAGTACAGTTGCACGATCTCGGCTCACTGCAACCTCCGCCTCCCAGG A G PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1047062666 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_128881 RMVar_hsa_circ_136062,RMVar_hsa_circ_94058,RMVar_hsa_circ_308976,RMVar_hsa_circ_293693,RMVar_hsa_circ_303523,RMVar_hsa_circ_136063,RMVar_hsa_circ_63943,RMVar_hsa_circ_370410,RMVar_hsa_circ_136061,RMVar_hsa_circ_334967,RMVar_hsa_circ_295327,RMVar_hsa_circ_136070,RMVar_hsa_circ_136071,RMVar_hsa_circ_136069,RMVar_hsa_circ_285554,RMVar_hsa_circ_136073,RMVar_hsa_circ_92230,RMVar_hsa_circ_136072,RMVar_hsa_circ_10979 36741 RMVar_ID_36741 Human_SNP_ID_33612194 A-to-I Human chr1 + 151235351 151235351 151235351 ATGATCTGCCTGCCTTGGCCTCCCAAAGTGCTAGGATTACAGGTGTGAGCCACCGCACCCGGCCT ATGATCTGCCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCACCCGGCCT A G PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1233805728 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136062,RMVar_hsa_circ_94058,RMVar_hsa_circ_308976,RMVar_hsa_circ_293693,RMVar_hsa_circ_63943,RMVar_hsa_circ_370410,RMVar_hsa_circ_136061,RMVar_hsa_circ_295327,RMVar_hsa_circ_136070,RMVar_hsa_circ_136071,RMVar_hsa_circ_285554,RMVar_hsa_circ_136073,RMVar_hsa_circ_92230,RMVar_hsa_circ_136072,RMVar_hsa_circ_136078,RMVar_hsa_circ_374067,RMVar_hsa_circ_29605,RMVar_hsa_circ_285611,RMVar_hsa_circ_136079 36742 RMVar_ID_36742 Human_SNP_ID_33612692 A-to-I Human chr1 + 151237009 151237009 151237009 GCCACCACACCCAGCTAATTTTTTGTATTTTTAGTAGAGAAGGGGTTTCATCATGTTGGGCAAAC GCCACCACACCCAGCTAATTTTTTGTATTTTTGGTAGAGAAGGGGTTTCATCATGTTGGGCAAAC A G PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs755088863 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136062,RMVar_hsa_circ_94058,RMVar_hsa_circ_293693,RMVar_hsa_circ_63943,RMVar_hsa_circ_370410,RMVar_hsa_circ_136061,RMVar_hsa_circ_136071,RMVar_hsa_circ_92230,RMVar_hsa_circ_136072,RMVar_hsa_circ_136078,RMVar_hsa_circ_374067,RMVar_hsa_circ_285611,RMVar_hsa_circ_136079 36743 RMVar_ID_36743 Human_SNP_ID_33612798 A-to-I Human chr1 + 151237496 151237496 151237496 CAGCCTGAGCATCATGATGAGACCTCATCACTACAAAAACTCAAAAATTACCTGAGTGTGATGGT CAGCCTGAGCATCATGATGAGACCTCATCACTGCAAAAACTCAAAAATTACCTGAGTGTGATGGT A G PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1223691434 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17725544 RMVar_hsa_circ_136062,RMVar_hsa_circ_94058,RMVar_hsa_circ_293693,RMVar_hsa_circ_63943,RMVar_hsa_circ_370410,RMVar_hsa_circ_136061,RMVar_hsa_circ_136071,RMVar_hsa_circ_92230,RMVar_hsa_circ_136072,RMVar_hsa_circ_136078,RMVar_hsa_circ_374067,RMVar_hsa_circ_285611,RMVar_hsa_circ_136079 36744 RMVar_ID_36744 Human_SNP_ID_33612806 A-to-I Human chr1 + 151237549 151237549 151237549 GAGTGTGATGGTGAGCACCTGTGGTCCCAGCTACTCAGGAGGCTGATGAGGCAGAATTGCTTGAG GAGTGTGATGGTGAGCACCTGTGGTCCCAGCTGCTCAGGAGGCTGATGAGGCAGAATTGCTTGAG A G PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1337661564 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136062,RMVar_hsa_circ_94058,RMVar_hsa_circ_293693,RMVar_hsa_circ_63943,RMVar_hsa_circ_370410,RMVar_hsa_circ_136061,RMVar_hsa_circ_136071,RMVar_hsa_circ_92230,RMVar_hsa_circ_136072,RMVar_hsa_circ_136078,RMVar_hsa_circ_374067,RMVar_hsa_circ_285611,RMVar_hsa_circ_136079 36745 RMVar_ID_36745 Human_SNP_ID_33615662 A-to-I Human chr1 - 151248510 151248510 151248510 GAGCAATCACTACTCTTCTCTTCATAAACACCATGGCTCTTCTGAGGGAACTCTACGAATAGGCA GAGCAATCACTACTCTTCTCTTCATAAACACCGTGGCTCTTCTGAGGGAACTCTACGAATAGGCA T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs587600805 Functional Loss SNV dbSNP153 33..33 33 - - - 36746 RMVar_ID_36746 Human_SNP_ID_33617757 A-to-I Human chr1 + 151256080 151256080 151256080 CTTTTGAAAAGTGTCTGGCTGGGGCGTGGCTCAGGCCTGTAATCCCAGCACTTTGGAAGGCTGAA CTTTTGAAAAGTGTCTGGCTGGGGCGTGGCTCCGGCCTGTAATCCCAGCACTTTGGAAGGCTGAA A C PSMD4 Ensembl:ENSG00000159352 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1452540142 Functional Loss SNV dbSNP153 33..33 33 - - - 36747 RMVar_ID_36747 Human_SNP_ID_33618021 A-to-I Human chr1 + 151256651 151256651 151256651 TAGAGACGGGGTTTCATCATGTTGGCCAGGCTAGTCTCAAACTGCTGAGCTCAGGTGATCCACCC TAGAGACGGGGTTTCATCATGTTGGCCAGGCTGGTCTCAAACTGCTGAGCTCAGGTGATCCACCC A G PSMD4 Ensembl:ENSG00000159352 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1267731135 Functional Loss SNV dbSNP153 33..33 33 - - - 36748 RMVar_ID_36748 Human_SNP_ID_33618544 A-to-I Human chr1 + 151258663 151258663 151258663 TTGTATTTTTTGTAGAGATGGGGTTTTGTCATATTGATTAGGCTGGTCTCGAACTCTTGGGCTCA TTGTATTTTTTGTAGAGATGGGGTTTTGTCATGTTGATTAGGCTGGTCTCGAACTCTTGGGCTCA A G PSMD4 Ensembl:ENSG00000159352 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs587614658 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10578325 36749 RMVar_ID_36749 Human_SNP_ID_33618577 A-to-I Human chr1 + 151258808 151258808 151258808 AATAAAGGTTTTGGCGGTAATCCCAGCTACTTAGGAGGCTGAGGCAGGAGAAGGGGTTAAGCCCA AATAAAGGTTTTGGCGGTAATCCCAGCTACTTTGGAGGCTGAGGCAGGAGAAGGGGTTAAGCCCA A T PSMD4 Ensembl:ENSG00000159352 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1558320287 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5689372 36750 RMVar_ID_36750 Human_SNP_ID_33618604 A-to-I Human chr1 + 151258952 151258952 151258952 AATATGTGAAATGGCCAGGTGCGGTGGCTTACACCTGTAATCCCAGCACTTTGAGAGGTTGAGGT AATATGTGAAATGGCCAGGTGCGGTGGCTTACGCCTGTAATCCCAGCACTTTGAGAGGTTGAGGT A G PSMD4 Ensembl:ENSG00000159352 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1160180646 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10578341 36751 RMVar_ID_36751 Human_SNP_ID_33618629 A-to-I Human chr1 + 151259032 151259032 151259032 GGTCAGGAGCTCAAGACCAACCTGGCCAACATAGTGAAACCCCGTCTCTACTAAAAATACAAAAA GGTCAGGAGCTCAAGACCAACCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAA A G PSMD4 Ensembl:ENSG00000159352 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs137899083 Functional Loss SNV dbSNP153 33..33 33 - - - 36752 RMVar_ID_36752 Human_SNP_ID_33618772 A-to-I Human chr1 + 151259660 151259660 151259660 CCTGTAATCCCAGCACTTTGAGAGGCCAAGGCAGGAGGACTACATGAGTCTAGGAGTTTGTGACT CCTGTAATCCCAGCACTTTGAGAGGCCAAGGCGGGAGGACTACATGAGTCTAGGAGTTTGTGACT A G PSMD4 Ensembl:ENSG00000159352 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1350654821 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10578369 36753 RMVar_ID_36753 Human_SNP_ID_33619008 A-to-I Human chr1 + 151260653 151260647 151260653 CACCTCTCAGGTTCAGGTGATTCTCCTGCCTCAGCCACCCGAATAGCTGGGATTACAGGTGCCTG CACCTCTCAGGTTCAGGTGATTCTCCT______GCCACCCGAATAGCTGGGATTACAGGTGCCTG TGCCTCA T PSMD4 Ensembl:ENSG00000159352 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs767490867 Functional Loss DEL dbSNP153 28..33 33 - - - 36754 RMVar_ID_36754 Human_SNP_ID_33619085 A-to-I Human chr1 + 151260949 151260949 151260949 CTCACTGCAACCTCGGCCTCCCGGGTTCAAGCAATTCTCCTGCCTCAACCTCCTGAGTAGCTAGG CTCACTGCAACCTCGGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCAACCTCCTGAGTAGCTAGG A G PSMD4 Ensembl:ENSG00000159352 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs192841539 Functional Loss SNV dbSNP153 33..33 33 - - - 36755 RMVar_ID_36755 Human_SNP_ID_33619298 A-to-I Human chr1 + 151261767 151261767 151261767 CTTGAGCTCAGAAGTTCAAGACCAGCTTGGGCAACATAGCTAGATCCCTGTCTCTACAAAAAAAA CTTGAGCTCAGAAGTTCAAGACCAGCTTGGGCCACATAGCTAGATCCCTGTCTCTACAAAAAAAA A C PSMD4 Ensembl:ENSG00000159352 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1309575111 Functional Loss SNV dbSNP153 33..33 33 - - - 36756 RMVar_ID_36756 Human_SNP_ID_33624138 A-to-I Human chr1 - 151279722 151279722 151279722 GCCCTGGAGTTCGAGACTAGCCTGTGCAACACAGCAGGACTCTGCCTCTACAGAATATTTGGAAA GCCCTGGAGTTCGAGACTAGCCTGTGCAACACTGCAGGACTCTGCCTCTACAGAATATTTGGAAA T A ZNF687-AS1 Ensembl:ENSG00000232671 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1419930260 Functional Loss SNV dbSNP153 33..33 33 - - - 36757 RMVar_ID_36757 Human_SNP_ID_33629308 A-to-I Human chr1 - 151296083 151296083 151296083 CGCCACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATCTTGGCCAGGC CGCCACCACGCCCAGCTAATTTTTGTATTTTTGGTAGAGACGGGGTTTCACCATCTTGGCCAGGC T C PI4KB Ensembl:ENSG00000143393 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1465865376 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44726,RMVar_hsa_circ_73523 36758 RMVar_ID_36758 Human_SNP_ID_33629311 A-to-I Human chr1 - 151296098 151296098 151296098 GGGATTACAGGCATGCGCCACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCA GGGATTACAGGCATGCGCCACCACGCCCAGCTGATTTTTGTATTTTTAGTAGAGACGGGGTTTCA T C PI4KB Ensembl:ENSG00000143393 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1404403467 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44726,RMVar_hsa_circ_73523 36759 RMVar_ID_36759 Human_SNP_ID_33629330 A-to-I Human chr1 - 151296146 151296146 151296146 GCCTCCCAGAGTTCAAGTGATTCTCCCACCTCAGCCTCCTGATTAGCTGGGATTACAGGCATGCG GCCTCCCAGAGTTCAAGTGATTCTCCCACCTCCGCCTCCTGATTAGCTGGGATTACAGGCATGCG T G PI4KB Ensembl:ENSG00000143393 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1010398630 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44726,RMVar_hsa_circ_73523 36760 RMVar_ID_36760 Human_SNP_ID_33629336 A-to-I Human chr1 - 151296184 151296184 151296184 GGAGTGCAGTGGCGTGATCTCGGCTCACTGTAACCTCTGCCTCCCAGAGTTCAAGTGATTCTCCC GGAGTGCAGTGGCGTGATCTCGGCTCACTGTATCCTCTGCCTCCCAGAGTTCAAGTGATTCTCCC T A PI4KB Ensembl:ENSG00000143393 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1219509218 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44726,RMVar_hsa_circ_73523 36761 RMVar_ID_36761 Human_SNP_ID_33634542 A-to-I Human chr1 - 151317937 151317937 151317937 GAGCATGATGGCACACACCTAAAGTCCTAGCTACTCGGGAGGCTGAGGCAGGAGGATGCCTTGAG GAGCATGATGGCACACACCTAAAGTCCTAGCTGCTCGGGAGGCTGAGGCAGGAGGATGCCTTGAG T C PI4KB Ensembl:ENSG00000143393 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049076248 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44726,RMVar_hsa_circ_348638,RMVar_hsa_circ_345443 36762 RMVar_ID_36762 Human_SNP_ID_33635930 A-to-I Human chr1 - 151323680 151323680 151323680 TCGTTCTGTCGCCCAGGCTAGAGTGCAGTGGCACGATCTCGGCTCACTGCAACCTCTGCCTCAGG TCGTTCTGTCGCCCAGGCTAGAGTGCAGTGGCTCGATCTCGGCTCACTGCAACCTCTGCCTCAGG T A PI4KB Ensembl:ENSG00000143393 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1160934318 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44726,RMVar_hsa_circ_348638,RMVar_hsa_circ_345443 36763 RMVar_ID_36763 Human_SNP_ID_33639338 A-to-I Human chr1 - 151337744 151337744 151337744 CACCCGCCATGGCCTCCCAAAGTGTTGGGATTACAGGTGTGAGCCAGCGTGCCTTGCCTATTTTA CACCCGCCATGGCCTCCCAAAGTGTTGGGATTCCAGGTGTGAGCCAGCGTGCCTTGCCTATTTTA T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1401124054 Functional Loss SNV dbSNP153 33..33 33 - - - 36764 RMVar_ID_36764 Human_SNP_ID_33639380 A-to-I Human chr1 - 151337965 151337965 151337965 GGCGTCTTGCTCTGTCACCCATGTTGGAGCGCAGTGGTGCAGTCTCAGCCCACTGCAACCTCTGC GGCGTCTTGCTCTGTCACCCATGTTGGAGCGCGGTGGTGCAGTCTCAGCCCACTGCAACCTCTGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs897233304 Functional Loss SNV dbSNP153 33..33 33 - - - 36765 RMVar_ID_36765 Human_SNP_ID_33646031 A-to-I Human chr1 - 151364660 151364660 151364660 ATGCTGCAGGTTGATGTAGACACAGTAAAAGGAGGGCTGAAGTTGAACCCCAACTTCCTGGTGGA ATGCTGCAGGTTGATGTAGACACAGTAAAAGGTGGGCTGAAGTTGAACCCCAACTTCCTGGTGGA T A SELENBP1 Ensembl:ENSG00000143416 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1490170039 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_129482,Human_Splice_Rec_129502,Human_Splice_Rec_129522,Human_Splice_Rec_129542,Human_Splice_Rec_129554,Human_Splice_Rec_129576,Human_Splice_Rec_129592,Human_Splice_Rec_129612,Human_Splice_Rec_129634,Human_Splice_Rec_129656,Human_Splice_Rec_129674 RMVar_hsa_circ_87249,RMVar_hsa_circ_136109,RMVar_hsa_circ_85190,RMVar_hsa_circ_136108 36766 RMVar_ID_36766 Human_SNP_ID_33646032 A-to-I Human chr1 - 151364660 151364660 151364660 ATGCTGCAGGTTGATGTAGACACAGTAAAAGGAGGGCTGAAGTTGAACCCCAACTTCCTGGTGGA ATGCTGCAGGTTGATGTAGACACAGTAAAAGGGGGGCTGAAGTTGAACCCCAACTTCCTGGTGGA T C SELENBP1 Ensembl:ENSG00000143416 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1490170039 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_129482,Human_Splice_Rec_129502,Human_Splice_Rec_129522,Human_Splice_Rec_129542,Human_Splice_Rec_129554,Human_Splice_Rec_129576,Human_Splice_Rec_129592,Human_Splice_Rec_129612,Human_Splice_Rec_129634,Human_Splice_Rec_129656,Human_Splice_Rec_129674 RMVar_hsa_circ_87249,RMVar_hsa_circ_136109,RMVar_hsa_circ_85190,RMVar_hsa_circ_136108 36767 RMVar_ID_36767 Human_SNP_ID_33646882 A-to-I Human chr1 - 151367108 151367108 151367108 GAACTCCTGACCTCAAGTGATCCGCCCGCCTCAGCCTCTCAAAGGGCTGGGATTACTGGCATGAG GAACTCCTGACCTCAAGTGATCCGCCCGCCTCGGCCTCTCAAAGGGCTGGGATTACTGGCATGAG T C SELENBP1 Ensembl:ENSG00000143416 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs914606750 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_129706,Human_Splice_Rec_129707,Human_Splice_Rec_129720,Human_Splice_Rec_129721 36768 RMVar_ID_36768 Human_SNP_ID_33646883 A-to-I Human chr1 - 151367108 151367108 151367108 GAACTCCTGACCTCAAGTGATCCGCCCGCCTCAGCCTCTCAAAGGGCTGGGATTACTGGCATGAG GAACTCCTGACCTCAAGTGATCCGCCCGCCTCCGCCTCTCAAAGGGCTGGGATTACTGGCATGAG T G SELENBP1 Ensembl:ENSG00000143416 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs914606750 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_129706,Human_Splice_Rec_129707,Human_Splice_Rec_129720,Human_Splice_Rec_129721 36769 RMVar_ID_36769 Human_SNP_ID_33659122 A-to-I Human chr1 - 151413824 151413823 151413824 AAAAAATTACTTGGCTAGGCACAGTGGCTCATACCTGTAATTCTGGTACTTTGGGAGGCTGAGAT AAAAAATTACTTGGCTAGGCACAGTGGCTCAT_CCTGTAATTCTGGTACTTTGGGAGGCTGAGAT GT G POGZ Ensembl:ENSG00000143442 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1328657055 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5689795 RMVar_hsa_circ_91466,RMVar_hsa_circ_361867,RMVar_hsa_circ_136125,RMVar_hsa_circ_115332,RMVar_hsa_circ_136126,RMVar_hsa_circ_136127,RMVar_hsa_circ_357928,RMVar_hsa_circ_97435,RMVar_hsa_circ_136128 36770 RMVar_ID_36770 Human_SNP_ID_33659739 A-to-I Human chr1 - 151416125 151416125 151416125 CAGCTCACTGCAACCTCCGCGTCACAGGTTCAAGCAATTCTTCTGCCTCAGCCTCCCGAGTAGCT CAGCTCACTGCAACCTCCGCGTCACAGGTTCAGGCAATTCTTCTGCCTCAGCCTCCCGAGTAGCT T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1438959805 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91466,RMVar_hsa_circ_361867,RMVar_hsa_circ_136125,RMVar_hsa_circ_115332,RMVar_hsa_circ_136126,RMVar_hsa_circ_136127,RMVar_hsa_circ_357928,RMVar_hsa_circ_97435,RMVar_hsa_circ_136128 36771 RMVar_ID_36771 Human_SNP_ID_33661155 A-to-I Human chr1 - 151420457 151420457 151420457 AATACAAAAATTGGGTGTGGTGGCGCACGCCTATAGTCGTAGCTACTCAGGAGGTAGAGGTGGGA AATACAAAAATTGGGTGTGGTGGCGCACGCCTGTAGTCGTAGCTACTCAGGAGGTAGAGGTGGGA T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1347967108 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91466,RMVar_hsa_circ_361867,RMVar_hsa_circ_136125,RMVar_hsa_circ_115332,RMVar_hsa_circ_136126,RMVar_hsa_circ_136127,RMVar_hsa_circ_357928,RMVar_hsa_circ_97435,RMVar_hsa_circ_136128 36772 RMVar_ID_36772 Human_SNP_ID_33664615 A-to-I Human chr1 - 151434064 151434064 151434064 CCTCAAGTGATCTGCCTGCCTCGGCCTCCCAAAGTGCTGACATTATAGGCGTAAGCCACCACGCC CCTCAAGTGATCTGCCTGCCTCGGCCTCCCAAGGTGCTGACATTATAGGCGTAAGCCACCACGCC T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1159039487 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2062,RMVar_hsa_circ_357928,RMVar_hsa_circ_270364,RMVar_hsa_circ_136132,RMVar_hsa_circ_272073,RMVar_hsa_circ_136135,RMVar_hsa_circ_342536,RMVar_hsa_circ_369597,RMVar_hsa_circ_136137 36773 RMVar_ID_36773 Human_SNP_ID_33664694 A-to-I Human chr1 - 151434390 151434390 151434390 GGCTCACTGCACCCTCCACCTCCCAGGCTCAAACGATCCTCCCACCTCGGCCCCCCAAGTAGCTG GGCTCACTGCACCCTCCACCTCCCAGGCTCAAGCGATCCTCCCACCTCGGCCCCCCAAGTAGCTG T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1306330441 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2062,RMVar_hsa_circ_357928,RMVar_hsa_circ_270364,RMVar_hsa_circ_136132,RMVar_hsa_circ_272073,RMVar_hsa_circ_136135,RMVar_hsa_circ_342536,RMVar_hsa_circ_369597,RMVar_hsa_circ_136137 36774 RMVar_ID_36774 Human_SNP_ID_33664712 A-to-I Human chr1 - 151434467 151434467 151434467 GGTTTTCTTTGTTTTGTTCAAGATGGGGTCTCACTTTGTCACCCAGGCTGGAGTGCAGTAGTGGC GGTTTTCTTTGTTTTGTTCAAGATGGGGTCTCGCTTTGTCACCCAGGCTGGAGTGCAGTAGTGGC T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1453754536 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24752028 RMVar_hsa_circ_2062,RMVar_hsa_circ_357928,RMVar_hsa_circ_270364,RMVar_hsa_circ_136132,RMVar_hsa_circ_272073,RMVar_hsa_circ_136135,RMVar_hsa_circ_342536,RMVar_hsa_circ_369597,RMVar_hsa_circ_136137 36775 RMVar_ID_36775 Human_SNP_ID_33665266 A-to-I Human chr1 - 151436504 151436504 151436504 GGGAGGCGGAGGTTGCTGTGAGCTGAGATCGCACCACTGCACTCCAGCCTGGGCAACAAGAGGAA GGGAGGCGGAGGTTGCTGTGAGCTGAGATCGCGCCACTGCACTCCAGCCTGGGCAACAAGAGGAA T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1398990429 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2062,RMVar_hsa_circ_357928,RMVar_hsa_circ_270364,RMVar_hsa_circ_136132,RMVar_hsa_circ_272073,RMVar_hsa_circ_136135,RMVar_hsa_circ_342536,RMVar_hsa_circ_369597,RMVar_hsa_circ_136137 36776 RMVar_ID_36776 Human_SNP_ID_33665289 A-to-I Human chr1 - 151436555 151436555 151436555 CCTGCAATCCCAGCTATTAGGGAGGCTGAGGCAGGAGAATCGTTTGCACTCGGGAGGCGGAGGTT CCTGCAATCCCAGCTATTAGGGAGGCTGAGGCGGGAGAATCGTTTGCACTCGGGAGGCGGAGGTT T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1276615539 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2062,RMVar_hsa_circ_357928,RMVar_hsa_circ_270364,RMVar_hsa_circ_136132,RMVar_hsa_circ_272073,RMVar_hsa_circ_136135,RMVar_hsa_circ_342536,RMVar_hsa_circ_369597,RMVar_hsa_circ_136137 36777 RMVar_ID_36777 Human_SNP_ID_33665292 A-to-I Human chr1 - 151436581 151436581 151436581 AAATTAGCCAGGTGTGGTGGTGCATGCCTGCAATCCCAGCTATTAGGGAGGCTGAGGCAGGAGAA AAATTAGCCAGGTGTGGTGGTGCATGCCTGCAGTCCCAGCTATTAGGGAGGCTGAGGCAGGAGAA T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1374840320 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2062,RMVar_hsa_circ_357928,RMVar_hsa_circ_270364,RMVar_hsa_circ_136132,RMVar_hsa_circ_272073,RMVar_hsa_circ_136135,RMVar_hsa_circ_342536,RMVar_hsa_circ_369597,RMVar_hsa_circ_136137 36778 RMVar_ID_36778 Human_SNP_ID_33665436 A-to-I Human chr1 - 151437147 151437147 151437147 CTTTGTTGCCCAGGCTGGAGTACAGTGGCGCAATCTCGGCTCACTGCAGCCTCTGCCTCCCAAGT CTTTGTTGCCCAGGCTGGAGTACAGTGGCGCATTCTCGGCTCACTGCAGCCTCTGCCTCCCAAGT T A POGZ Ensembl:ENSG00000143442 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs895017814 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2062,RMVar_hsa_circ_357928,RMVar_hsa_circ_270364,RMVar_hsa_circ_136132,RMVar_hsa_circ_272073,RMVar_hsa_circ_136135,RMVar_hsa_circ_342536,RMVar_hsa_circ_369597,RMVar_hsa_circ_136137 36779 RMVar_ID_36779 Human_SNP_ID_33665437 A-to-I Human chr1 - 151437147 151437147 151437147 CTTTGTTGCCCAGGCTGGAGTACAGTGGCGCAATCTCGGCTCACTGCAGCCTCTGCCTCCCAAGT CTTTGTTGCCCAGGCTGGAGTACAGTGGCGCAGTCTCGGCTCACTGCAGCCTCTGCCTCCCAAGT T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs895017814 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2062,RMVar_hsa_circ_357928,RMVar_hsa_circ_270364,RMVar_hsa_circ_136132,RMVar_hsa_circ_272073,RMVar_hsa_circ_136135,RMVar_hsa_circ_342536,RMVar_hsa_circ_369597,RMVar_hsa_circ_136137 36780 RMVar_ID_36780 Human_SNP_ID_33665577 A-to-I Human chr1 - 151437669 151437669 151437669 CGGCTCACTGCAACCTCTGTCTCCCTGGTTCAAGCGATTCTCATGCCTCACCCACCCCAGTAGCT CGGCTCACTGCAACCTCTGTCTCCCTGGTTCAGGCGATTCTCATGCCTCACCCACCCCAGTAGCT T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs574121749 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2062,RMVar_hsa_circ_357928,RMVar_hsa_circ_270364,RMVar_hsa_circ_136132,RMVar_hsa_circ_272073,RMVar_hsa_circ_136135,RMVar_hsa_circ_342536,RMVar_hsa_circ_369597,RMVar_hsa_circ_136137 36781 RMVar_ID_36781 Human_SNP_ID_33665674 A-to-I Human chr1 - 151438128 151438128 151438128 TGGCCCACTGCAACCTCCACTTCCCGGGTTCAAGTAATTCTCTTGCCTCAGCCTCCTGAGTAGCT TGGCCCACTGCAACCTCCACTTCCCGGGTTCACGTAATTCTCTTGCCTCAGCCTCCTGAGTAGCT T G POGZ Ensembl:ENSG00000143442 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1245190944 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2062,RMVar_hsa_circ_357928,RMVar_hsa_circ_270364,RMVar_hsa_circ_136132,RMVar_hsa_circ_272073,RMVar_hsa_circ_136135,RMVar_hsa_circ_342536,RMVar_hsa_circ_369597,RMVar_hsa_circ_136137 36782 RMVar_ID_36782 Human_SNP_ID_33666802 A-to-I Human chr1 - 151442627 151442627 151442627 GACCCCCTGCAACCTCTGCCTCCTGGATTCAAACGATTCTCGTGCCTCAGCCTCCCAAGTAGCTG GACCCCCTGCAACCTCTGCCTCCTGGATTCAAGCGATTCTCGTGCCTCAGCCTCCCAAGTAGCTG T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1313203390 Functional Loss SNV dbSNP153 33..33 33 - - - 36783 RMVar_ID_36783 Human_SNP_ID_33667076 A-to-I Human chr1 - 151443552 151443552 151443552 GCACCACCACGCCCGGCTAATTTTATGTTTTTAGTAGAGATGGGTTTTCTCCATGTTGGTCAGGC GCACCACCACGCCCGGCTAATTTTATGTTTTTGGTAGAGATGGGTTTTCTCCATGTTGGTCAGGC T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs936503617 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8043531,Human_RBP_ID_10580623 36784 RMVar_ID_36784 Human_SNP_ID_33667080 A-to-I Human chr1 - 151443560 151443558 151443560 ACAGGCATGCACCACCACGCCCGGCTAATTTTATGTTTTTAGTAGAGATGGGTTTTCTCCATGTT ACAGGCATGCACCACCACGCCCGGCTAATTTT__GTTTTTAGTAGAGATGGGTTTTCTCCATGTT CAT C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1350297750 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_8043531,Human_RBP_ID_10580623 36785 RMVar_ID_36785 Human_SNP_ID_33668139 A-to-I Human chr1 - 151447286 151447286 151447286 TTCACTGCAACCTCCGCCTCCTGGGTTCAAGCAATTCTCCTGTTTCAGCCTCCTGAGTAGCTGGA TTCACTGCAACCTCCGCCTCCTGGGTTCAAGCGATTCTCCTGTTTCAGCCTCCTGAGTAGCTGGA T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1335617996 Functional Loss SNV dbSNP153 33..33 33 - - - 36786 RMVar_ID_36786 Human_SNP_ID_33668293 A-to-I Human chr1 - 151447736 151447736 151447736 CCTATAATCCCAGCACTTTGGGAATCTGAGGCAGGTGTGTTGCTTGAGTCCAGGAGTTTGAGACC CCTATAATCCCAGCACTTTGGGAATCTGAGGCGGGTGTGTTGCTTGAGTCCAGGAGTTTGAGACC T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1138548 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24587950 36787 RMVar_ID_36787 Human_SNP_ID_33668304 A-to-I Human chr1 - 151447765 151447765 151447765 ACATCAAAAGCTGGGCACAGTGGCTCATACCTATAATCCCAGCACTTTGGGAATCTGAGGCAGGT ACATCAAAAGCTGGGCACAGTGGCTCATACCTGTAATCCCAGCACTTTGGGAATCTGAGGCAGGT T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1138546 Functional Loss SNV dbSNP153 33..33 33 - - - 36788 RMVar_ID_36788 Human_SNP_ID_33668305 A-to-I Human chr1 - 151447779 151447779 151447779 GCATGGATCAAAACACATCAAAAGCTGGGCACAGTGGCTCATACCTATAATCCCAGCACTTTGGG GCATGGATCAAAACACATCAAAAGCTGGGCACGGTGGCTCATACCTATAATCCCAGCACTTTGGG T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE38233;GSE107867 cultured B-cells;ASD brains,cerebellum - 24183664,30559470 RNA-Seq:(High) rs1448296682 Functional Loss SNV dbSNP153 33..33 33 - - - 36789 RMVar_ID_36789 Human_SNP_ID_33668436 A-to-I Human chr1 - 151448382 151448382 151448382 GTCTCGAACTCCTGAACTCAGGTAATCCTCTCACCTCAGCCTCCCGAAGTGCTAGGATTGCAGAT GTCTCGAACTCCTGAACTCAGGTAATCCTCTCGCCTCAGCCTCCCGAAGTGCTAGGATTGCAGAT T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs996484877 Functional Loss SNV dbSNP153 33..33 33 - - - 36790 RMVar_ID_36790 Human_SNP_ID_33668438 A-to-I Human chr1 - 151448391 151448391 151448391 CACAAGCTGGTCTCGAACTCCTGAACTCAGGTAATCCTCTCACCTCAGCCTCCCGAAGTGCTAGG CACAAGCTGGTCTCGAACTCCTGAACTCAGGTGATCCTCTCACCTCAGCCTCCCGAAGTGCTAGG T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs977747743 Functional Loss SNV dbSNP153 33..33 33 - - - 36791 RMVar_ID_36791 Human_SNP_ID_33668439 A-to-I Human chr1 - 151448395 151448395 151448395 GTTGCACAAGCTGGTCTCGAACTCCTGAACTCAGGTAATCCTCTCACCTCAGCCTCCCGAAGTGC GTTGCACAAGCTGGTCTCGAACTCCTGAACTCCGGTAATCCTCTCACCTCAGCCTCCCGAAGTGC T G POGZ Ensembl:ENSG00000143442 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 29129909,30559470 RNA-Seq:(High) rs562880939 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10580817 36792 RMVar_ID_36792 Human_SNP_ID_33668447 A-to-I Human chr1 - 151448419 151448419 151448419 TTAATAGATATGAGGTCTCTCTCTGTTGCACAAGCTGGTCTCGAACTCCTGAACTCAGGTAATCC TTAATAGATATGAGGTCTCTCTCTGTTGCACAGGCTGGTCTCGAACTCCTGAACTCAGGTAATCC T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs1372118323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10580817 36793 RMVar_ID_36793 Human_SNP_ID_33668538 A-to-I Human chr1 - 151448782 151448782 151448782 CAGCTCACTTCAGCCTCCACCTCCTGGACTTAAGAGATTCTCCCACCTCAGCCTGTTGAGTAGCT CAGCTCACTTCAGCCTCCACCTCCTGGACTTACGAGATTCTCCCACCTCAGCCTGTTGAGTAGCT T G POGZ Ensembl:ENSG00000143442 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1210265550 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5690028,Human_RBP_ID_10580832,Human_RBP_ID_24587955 36794 RMVar_ID_36794 Human_SNP_ID_33668782 A-to-I Human chr1 - 151449653 151449653 151449653 TGACCTCGTGATCCGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGTGC TGACCTCGTGATCCGCCCACCTCGGCCTCCCAGAGTGCTGGGATTACAGGCGTGAGCCACTGTGC T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1440172981 Functional Loss SNV dbSNP153 33..33 33 - - - 36795 RMVar_ID_36795 Human_SNP_ID_33668787 A-to-I Human chr1 - 151449667 151449667 151449667 TGGTCTTGATCTCCTGACCTCGTGATCCGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGC TGGTCTTGATCTCCTGACCTCGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGC T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1384660613 Functional Loss SNV dbSNP153 33..33 33 - - - 36796 RMVar_ID_36796 Human_SNP_ID_33668825 A-to-I Human chr1 - 151449774 151449774 151449774 CTCCTGCCCCAGCCTCCCGAGTAGCTGGGATTACAGGCGGCCGCCACCACGCCTGGCTAATTTTT CTCCTGCCCCAGCCTCCCGAGTAGCTGGGATTGCAGGCGGCCGCCACCACGCCTGGCTAATTTTT T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1215199310 Functional Loss SNV dbSNP153 33..33 33 - - - 36797 RMVar_ID_36797 Human_SNP_ID_33668959 A-to-I Human chr1 - 151450170 151450170 151450170 AAAACTAGCCAGCCGTGGTGGTGGGCACCTGTAGTCCCAGCTACTTGGGAGACTGAAACAGGAGA AAAACTAGCCAGCCGTGGTGGTGGGCACCTGTGGTCCCAGCTACTTGGGAGACTGAAACAGGAGA T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1331616041 Functional Loss SNV dbSNP153 33..33 33 - - - 36798 RMVar_ID_36798 Human_SNP_ID_33669016 A-to-I Human chr1 - 151450402 151450402 151450402 GCTGCAGTGAGTTGAGATCGCGCCACTGCACTACAGCCCAGGCGACAAAGACCCTGTGACCTAAA GCTGCAGTGAGTTGAGATCGCGCCACTGCACTGCAGCCCAGGCGACAAAGACCCTGTGACCTAAA T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1384935278 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10580868 36799 RMVar_ID_36799 Human_SNP_ID_33669028 A-to-I Human chr1 - 151450444 151450444 151450444 GGAGGCTGAGACGGGAGGATTGCTTGAGCCCAAGAGGTCGAGGCTGCAGTGAGTTGAGATCGCGC GGAGGCTGAGACGGGAGGATTGCTTGAGCCCAGGAGGTCGAGGCTGCAGTGAGTTGAGATCGCGC T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1486580060 Functional Loss SNV dbSNP153 33..33 33 - - - 36800 RMVar_ID_36800 Human_SNP_ID_33669052 A-to-I Human chr1 - 151450533 151450533 151450533 GCCTGGGCAATATGGCAAAACTCTAGCTTTATAGAAAATACAAAAATTAACCAGGCGTGGTAGCA GCCTGGGCAATATGGCAAAACTCTAGCTTTATCGAAAATACAAAAATTAACCAGGCGTGGTAGCA T G POGZ Ensembl:ENSG00000143442 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs987566172 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10580869 36801 RMVar_ID_36801 Human_SNP_ID_33669058 A-to-I Human chr1 - 151450572 151450572 151450572 AAGGCAAGCAGATCACTTGAGTCCTGAAGTTCAAGACCAGCCTGGGCAATATGGCAAAACTCTAG AAGGCAAGCAGATCACTTGAGTCCTGAAGTTCGAGACCAGCCTGGGCAATATGGCAAAACTCTAG T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1196589867 Functional Loss SNV dbSNP153 33..33 33 - - - 36802 RMVar_ID_36802 Human_SNP_ID_33669188 A-to-I Human chr1 - 151451073 151451073 151451073 GGATTACAGGCGTGTGCCACCACACCTGGCTAATTTTTGTATTTTTTTTTTTTAGTAGAGACGGG GGATTACAGGCGTGTGCCACCACACCTGGCTAGTTTTTGTATTTTTTTTTTTTAGTAGAGACGGG T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1401250764 Functional Loss SNV dbSNP153 33..33 33 - - - 36803 RMVar_ID_36803 Human_SNP_ID_33669285 A-to-I Human chr1 - 151451419 151451419 151451419 GAGAGGCTGAAGCAAGAGAATCGCTTGCACCCAGGAGGTGAAGGTTGCAGTGAGCTGAGATCGCG GAGAGGCTGAAGCAAGAGAATCGCTTGCACCCGGGAGGTGAAGGTTGCAGTGAGCTGAGATCGCG T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs534787790 Functional Loss SNV dbSNP153 33..33 33 - - - 36804 RMVar_ID_36804 Human_SNP_ID_33669290 A-to-I Human chr1 - 151451437 151451437 151451437 CTGTAATTACAGCTCCTTGAGAGGCTGAAGCAAGAGAATCGCTTGCACCCAGGAGGTGAAGGTTG CTGTAATTACAGCTCCTTGAGAGGCTGAAGCAGGAGAATCGCTTGCACCCAGGAGGTGAAGGTTG T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs971706910 Functional Loss SNV dbSNP153 33..33 33 - - - 36805 RMVar_ID_36805 Human_SNP_ID_33669291 A-to-I Human chr1 - 151451437 151451437 151451437 CTGTAATTACAGCTCCTTGAGAGGCTGAAGCAAGAGAATCGCTTGCACCCAGGAGGTGAAGGTTG CTGTAATTACAGCTCCTTGAGAGGCTGAAGCACGAGAATCGCTTGCACCCAGGAGGTGAAGGTTG T G POGZ Ensembl:ENSG00000143442 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs971706910 Functional Loss SNV dbSNP153 33..33 33 - - - 36806 RMVar_ID_36806 Human_SNP_ID_33669315 A-to-I Human chr1 - 151451527 151451527 151451527 GAGGTCAGGAGTTGAAGACCAGCCTGACCAACATGATGAAACCCCATCTCTACTAAAAGTACAAA GAGGTCAGGAGTTGAAGACCAGCCTGACCAACGTGATGAAACCCCATCTCTACTAAAAGTACAAA T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1273854981 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24587974 36807 RMVar_ID_36807 Human_SNP_ID_33669323 A-to-I Human chr1 - 151451558 151451546 151451558 ACTTTGGGAGACTGAGGCGGGTGGATCACCTGAGGTCAGGAGTTGAAGACCAGCCTGACCAACAT ACTTTGGGAGACTGAGGCGGGTGGATCACCTG____________GAAGACCAGCCTGACCAACAT CAACTCCTGACCT C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1382468658 Functional Loss DEL dbSNP153 33..44 33 - - - 36808 RMVar_ID_36808 Human_SNP_ID_33669456 A-to-I Human chr1 - 151452034 151452034 151452034 GGAGTGCAATTGCACCATCTCGGCTCACTGCAACCTCCACCTCCCGGGTTCAAGCAATTCTCCTG GGAGTGCAATTGCACCATCTCGGCTCACTGCAGCCTCCACCTCCCGGGTTCAAGCAATTCTCCTG T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973162318 Functional Loss SNV dbSNP153 33..33 33 - - - 36809 RMVar_ID_36809 Human_SNP_ID_33669457 A-to-I Human chr1 - 151452034 151452034 151452034 GGAGTGCAATTGCACCATCTCGGCTCACTGCAACCTCCACCTCCCGGGTTCAAGCAATTCTCCTG GGAGTGCAATTGCACCATCTCGGCTCACTGCACCCTCCACCTCCCGGGTTCAAGCAATTCTCCTG T G POGZ Ensembl:ENSG00000143442 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973162318 Functional Loss SNV dbSNP153 33..33 33 - - - 36810 RMVar_ID_36810 Human_SNP_ID_33669603 A-to-I Human chr1 - 151452426 151452426 151452426 GGATCACCTGAGCCCAGGAGGTTGAGGCTGCAATAAGCCGTGATTGTGCCACTGCACTCCAGCCT GGATCACCTGAGCCCAGGAGGTTGAGGCTGCAGTAAGCCGTGATTGTGCCACTGCACTCCAGCCT T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs906142182 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10580898 36811 RMVar_ID_36811 Human_SNP_ID_33669604 A-to-I Human chr1 - 151452426 151452426 151452426 GGATCACCTGAGCCCAGGAGGTTGAGGCTGCAATAAGCCGTGATTGTGCCACTGCACTCCAGCCT GGATCACCTGAGCCCAGGAGGTTGAGGCTGCACTAAGCCGTGATTGTGCCACTGCACTCCAGCCT T G POGZ Ensembl:ENSG00000143442 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs906142182 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10580898 36812 RMVar_ID_36812 Human_SNP_ID_33669616 A-to-I Human chr1 - 151452489 151452489 151452489 TCTATAAGAAAATATCAAAATAGCCCACCTGTAGTGACAACTACTTGGGAGGCTGAGGCAGGAGG TCTATAAGAAAATATCAAAATAGCCCACCTGTGGTGACAACTACTTGGGAGGCTGAGGCAGGAGG T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs887020615 Functional Loss SNV dbSNP153 33..33 33 - - - 36813 RMVar_ID_36813 Human_SNP_ID_33669663 A-to-I Human chr1 - 151452609 151452609 151452609 CGCCTGCATTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCGCCTGGTGACAGGAT CGCCTGCATTGGCCTCCCAAAGTGCTGGGATTGCAGGCGTGAGCCACTGCGCCTGGTGACAGGAT T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,temporal_cortex - 29129909,30559470 RNA-Seq:(High) rs532608920 Functional Loss SNV dbSNP153 33..33 33 - - - 36814 RMVar_ID_36814 Human_SNP_ID_33669685 A-to-I Human chr1 - 151452701 151452701 151452701 AGCCACCACGCATGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACTGTGTTGGCCAGGC AGCCACCACGCATGGCTAATTTTTGTATTTTTGGTAGAGACGGGGTTTCACTGTGTTGGCCAGGC T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs780693609 Functional Loss SNV dbSNP153 33..33 33 - - - 36815 RMVar_ID_36815 Human_SNP_ID_33669690 A-to-I Human chr1 - 151452716 151452716 151452716 GGGACTGCAGGCACCAGCCACCACGCATGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCA GGGACTGCAGGCACCAGCCACCACGCATGGCTGATTTTTGTATTTTTAGTAGAGACGGGGTTTCA T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1454963800 Functional Loss SNV dbSNP153 33..33 33 - - - 36816 RMVar_ID_36816 Human_SNP_ID_33669719 A-to-I Human chr1 - 151452807 151452807 151452807 TAGACTAGAGTGCAGTGGCACAATCTTGGCTCACTGCAACCTCTGCCTCCCGAATTCAAGCGATT TAGACTAGAGTGCAGTGGCACAATCTTGGCTCCCTGCAACCTCTGCCTCCCGAATTCAAGCGATT T G POGZ Ensembl:ENSG00000143442 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1197568751 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10580905 36817 RMVar_ID_36817 Human_SNP_ID_33669721 A-to-I Human chr1 - 151452820 151452820 151452820 TCGCTCTGTTGCCTAGACTAGAGTGCAGTGGCACAATCTTGGCTCACTGCAACCTCTGCCTCCCG TCGCTCTGTTGCCTAGACTAGAGTGCAGTGGCGCAATCTTGGCTCACTGCAACCTCTGCCTCCCG T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1177080205 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10580905 36818 RMVar_ID_36818 Human_SNP_ID_33669782 A-to-I Human chr1 - 151453087 151453087 151453087 TGAAACCTGTCTCTACTAAAAATACAAAAATTAGCTGGGCGTTGTGGCGCATGCATGTAATCCCA TGAAACCTGTCTCTACTAAAAATACAAAAATTGGCTGGGCGTTGTGGCGCATGCATGTAATCCCA T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1183164758 Functional Loss SNV dbSNP153 33..33 33 - - - 36819 RMVar_ID_36819 Human_SNP_ID_33669795 A-to-I Human chr1 - 151453123 151453123 151453123 AAGGTCAGGAGTTCAAGACCAGCCTGACCAACATGGTGAAACCTGTCTCTACTAAAAATACAAAA AAGGTCAGGAGTTCAAGACCAGCCTGACCAACGTGGTGAAACCTGTCTCTACTAAAAATACAAAA T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs993515097 Functional Loss SNV dbSNP153 33..33 33 - - - 36820 RMVar_ID_36820 Human_SNP_ID_33670234 A-to-I Human chr1 - 151454905 151454905 151454905 TGGGGTTTCACCATATTGATCAGGCTGGTCTCAAACTCCTGACCTCTTGATCGACCCGCCTTGGC TGGGGTTTCACCATATTGATCAGGCTGGTCTCGAACTCCTGACCTCTTGATCGACCCGCCTTGGC T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE100210;GSE107867;GSE107867 HepG2 cell line;ASD brains,cerebellum;ASD brains,temporal_cortex - 29129909,30559470,30559470 RNA-Seq:(High) rs796286598 Functional Loss SNV dbSNP153 33..33 33 - - - 36821 RMVar_ID_36821 Human_SNP_ID_33670236 A-to-I Human chr1 - 151454925 151454925 151454925 TTTTTGTATTTTTCTAGAGATGGGGTTTCACCATATTGATCAGGCTGGTCTCAAACTCCTGACCT TTTTTGTATTTTTCTAGAGATGGGGTTTCACCTTATTGATCAGGCTGGTCTCAAACTCCTGACCT T A POGZ Ensembl:ENSG00000143442 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs560209880 Functional Loss SNV dbSNP153 33..33 33 - - - 36822 RMVar_ID_36822 Human_SNP_ID_33670263 A-to-I Human chr1 - 151455007 151455007 151455007 CGCCTCCTGGGTTCAAGCGATTCTCCTCCTTCAGCTTCCTCAGTAGCTGGGATTACAGGCACGCG CGCCTCCTGGGTTCAAGCGATTCTCCTCCTTCGGCTTCCTCAGTAGCTGGGATTACAGGCACGCG T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1290239027 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_130067,Human_Splice_Rec_130081 36823 RMVar_ID_36823 Human_SNP_ID_33670272 A-to-I Human chr1 - 151455024 151455024 151455024 CGGCTCACTGCACCCTCCGCCTCCTGGGTTCAAGCGATTCTCCTCCTTCAGCTTCCTCAGTAGCT CGGCTCACTGCACCCTCCGCCTCCTGGGTTCACGCGATTCTCCTCCTTCAGCTTCCTCAGTAGCT T G POGZ Ensembl:ENSG00000143442 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1415083070 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_130067,Human_Splice_Rec_130081 36824 RMVar_ID_36824 Human_SNP_ID_33670306 A-to-I Human chr1 - 151455105 151455105 151455105 ATTCACAAAAACTTGTCTTTTTTTTTTTTTTGAGATGGAGTCTCGCTCTATTGCCCAGGCTGGAG ATTCACAAAAACTTGTCTTTTTTTTTTTTTTGTGATGGAGTCTCGCTCTATTGCCCAGGCTGGAG T A POGZ Ensembl:ENSG00000143442 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1325844715 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10580975,Human_RBP_ID_24588006 36825 RMVar_ID_36825 Human_SNP_ID_33670588 A-to-I Human chr1 - 151455993 151455993 151455993 CACTCCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGAAGGATTGTGTGAGCCCAGGAGTTGGA CACTCCTGTAATCCCAGCACTTTGGGAGGCCAGGGTGGAAGGATTGTGTGAGCCCAGGAGTTGGA T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1137942 Functional Loss SNV dbSNP153 33..33 33 - - - 36826 RMVar_ID_36826 Human_SNP_ID_33670594 A-to-I Human chr1 - 151456010 151456010 151456010 GGCCTAGCGTGGTGGCTCACTCCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGAAGGATTGTG GGCCTAGCGTGGTGGCTCACTCCTGTAATCCCGGCACTTTGGGAGGCCAAGGTGGAAGGATTGTG T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1137940 Functional Loss SNV dbSNP153 33..33 33 - - - 36827 RMVar_ID_36827 Human_SNP_ID_33670596 A-to-I Human chr1 - 151456015 151456015 151456015 TATTTGGCCTAGCGTGGTGGCTCACTCCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGAAGGA TATTTGGCCTAGCGTGGTGGCTCACTCCTGTAGTCCCAGCACTTTGGGAGGCCAAGGTGGAAGGA T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1137939 Functional Loss SNV dbSNP153 33..33 33 - - - 36828 RMVar_ID_36828 Human_SNP_ID_33670597 A-to-I Human chr1 - 151456016 151456016 151456016 CTATTTGGCCTAGCGTGGTGGCTCACTCCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGAAGG CTATTTGGCCTAGCGTGGTGGCTCACTCCTGTGATCCCAGCACTTTGGGAGGCCAAGGTGGAAGG T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1137938 Functional Loss SNV dbSNP153 33..33 33 - - - 36829 RMVar_ID_36829 Human_SNP_ID_33670599 A-to-I Human chr1 - 151456024 151456024 151456024 AGAAACTACTATTTGGCCTAGCGTGGTGGCTCACTCCTGTAATCCCAGCACTTTGGGAGGCCAAG AGAAACTACTATTTGGCCTAGCGTGGTGGCTCGCTCCTGTAATCCCAGCACTTTGGGAGGCCAAG T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1137936 Functional Loss SNV dbSNP153 33..33 33 - - - 36830 RMVar_ID_36830 Human_SNP_ID_33692696 A-to-I Human chr1 + 151544195 151544195 151544195 TAGATATGGGTTCTCACTATGTTGCCCAGGCTAGTCTTGAACTCCTGGTTTAAAGTAATCTTCCT TAGATATGGGTTCTCACTATGTTGCCCAGGCTGGTCTTGAACTCCTGGTTTAAAGTAATCTTCCT A G AL365436.2,TUFT1 Ensembl:ENSG00000232536,Ensembl:ENSG00000143367 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1222707181 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110647,RMVar_hsa_circ_136139 36831 RMVar_ID_36831 Human_SNP_ID_33693932 A-to-I Human chr1 + 151549821 151549821 151549821 TTGGCTCACTGCCGCCTTGACCTTATGAGCTCAATTGATCCTCTCACCTCAGCTTCCCTAGTAGC TTGGCTCACTGCCGCCTTGACCTTATGAGCTCTATTGATCCTCTCACCTCAGCTTCCCTAGTAGC A T AL365436.2,TUFT1 Ensembl:ENSG00000232536,Ensembl:ENSG00000143367 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1241603132 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110647,RMVar_hsa_circ_136139 36832 RMVar_ID_36832 Human_SNP_ID_33694142 A-to-I Human chr1 + 151550820 151550820 151550820 CACGGTGGTGCACGCCTGTAGTCCAGCTGCTTAGGAAGCTGAGATGAGAGGATCAATTGAGCCTG CACGGTGGTGCACGCCTGTAGTCCAGCTGCTTGGGAAGCTGAGATGAGAGGATCAATTGAGCCTG A G AL365436.2,TUFT1 Ensembl:ENSG00000232536,Ensembl:ENSG00000143367 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs986307728 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110647,RMVar_hsa_circ_136139 36833 RMVar_ID_36833 Human_SNP_ID_33696331 A-to-I Human chr1 + 151560336 151560336 151560336 TACTTGGGAGGCTGAGGCAGGAGAATTGCTTGAGCCCAGGAGACGGAGGCTGCAGTGAGCCAAGA TACTTGGGAGGCTGAGGCAGGAGAATTGCTTGGGCCCAGGAGACGGAGGCTGCAGTGAGCCAAGA A G AL365436.2,TUFT1 Ensembl:ENSG00000232536,Ensembl:ENSG00000143367 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1008957896 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110647,RMVar_hsa_circ_136139 36834 RMVar_ID_36834 Human_SNP_ID_33719411 A-to-I Human chr1 + 151652464 151652464 151652464 GGAGCCTTGCTCTGTCACCTAGGCTGGAGTGCAGTGGTGTGATCTCGGCTCACTGCAACCTCCGC GGAGCCTTGCTCTGTCACCTAGGCTGGAGTGCGGTGGTGTGATCTCGGCTCACTGCAACCTCCGC A G SNX27 Ensembl:ENSG00000143376 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs911058257 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_316646,RMVar_hsa_circ_324552,RMVar_hsa_circ_338220,RMVar_hsa_circ_324478,RMVar_hsa_circ_290690,RMVar_hsa_circ_315824,RMVar_hsa_circ_275696,RMVar_hsa_circ_136148,RMVar_hsa_circ_24291,RMVar_hsa_circ_270329,RMVar_hsa_circ_136150,RMVar_hsa_circ_136151,RMVar_hsa_circ_136149,RMVar_hsa_circ_136146,RMVar_hsa_circ_136147,RMVar_hsa_circ_136145 36835 RMVar_ID_36835 Human_SNP_ID_33720576 A-to-I Human chr1 + 151657210 151657210 151657210 CATTTTGTTTTTTTGAGACAGTGTGTCCTTCTATTGTCCAGGCTGGAGTGTAGTGGCAGGATCGT CATTTTGTTTTTTTGAGACAGTGTGTCCTTCTGTTGTCCAGGCTGGAGTGTAGTGGCAGGATCGT A G SNX27 Ensembl:ENSG00000143376 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs919308583 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_316646,RMVar_hsa_circ_324552,RMVar_hsa_circ_338220,RMVar_hsa_circ_324478,RMVar_hsa_circ_290690,RMVar_hsa_circ_315824,RMVar_hsa_circ_275696,RMVar_hsa_circ_136148,RMVar_hsa_circ_24291,RMVar_hsa_circ_270329,RMVar_hsa_circ_136150,RMVar_hsa_circ_136151,RMVar_hsa_circ_136149,RMVar_hsa_circ_136146,RMVar_hsa_circ_136147,RMVar_hsa_circ_136145 36836 RMVar_ID_36836 Human_SNP_ID_33749486 A-to-I Human chr1 - 151777384 151777384 151777384 TGGAGTGCAATGGTGCATTCTCGGCTCACTGCAACCTCCGCCTCCCAGGTTCGAGTGATTCTCAT TGGAGTGCAATGGTGCATTCTCGGCTCACTGCTACCTCCGCCTCCCAGGTTCGAGTGATTCTCAT T A TDRKH Ensembl:ENSG00000182134 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1168763119 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124134,RMVar_hsa_circ_136171,RMVar_hsa_circ_108927,RMVar_hsa_circ_136170,RMVar_hsa_circ_379018 36837 RMVar_ID_36837 Human_SNP_ID_33765817 A-to-I Human chr1 + 151843922 151843922 151843922 CTCCTGCCTCAGCCTCACAAGTAGCTGGGACTACAGGCGAGCACCACCATGCCCTGTTAATTTTT CTCCTGCCTCAGCCTCACAAGTAGCTGGGACTGCAGGCGAGCACCACCATGCCCTGTTAATTTTT A G C2CD4D-AS1 Ensembl:ENSG00000234614 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs765397676 Functional Loss SNV dbSNP153 33..33 33 - - - 36838 RMVar_ID_36838 Human_SNP_ID_33768279 A-to-I Human chr1 + 151854074 151854074 151854074 CTCACAGGCCGGGTGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGCGGA CTCACAGGCCGGGTGCGGTGGCTCACGCCTGTGATCCCAGCACTTTGGGAGGCCGAGGCGGCGGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1043364943 Functional Loss SNV dbSNP153 33..33 33 - - - 36839 RMVar_ID_36839 Human_SNP_ID_33768454 A-to-I Human chr1 + 151854540 151854540 151854540 CTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGACACACACCACCACACCCAGCTAAATTTT CTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTTCAGACACACACCACCACACCCAGCTAAATTTT A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1437964742 Functional Loss SNV dbSNP153 33..33 33 - - - 36840 RMVar_ID_36840 Human_SNP_ID_33768459 A-to-I Human chr1 + 151854562 151854562 151854562 AGCTGGGATTACAGACACACACCACCACACCCAGCTAAATTTTGTATATTTTTTTTAGTAGAGAT AGCTGGGATTACAGACACACACCACCACACCCGGCTAAATTTTGTATATTTTTTTTAGTAGAGAT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1210207890 Functional Loss SNV dbSNP153 33..33 33 - - - 36841 RMVar_ID_36841 Human_SNP_ID_33768469 A-to-I Human chr1 + 151854586 151854586 151854586 CCACACCCAGCTAAATTTTGTATATTTTTTTTAGTAGAGATGGGGTTTTGCCATGTTAGCCAGGC CCACACCCAGCTAAATTTTGTATATTTTTTTTGGTAGAGATGGGGTTTTGCCATGTTAGCCAGGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1407115972 Functional Loss SNV dbSNP153 33..33 33 - - - 36842 RMVar_ID_36842 Human_SNP_ID_33768580 A-to-I Human chr1 + 151855088 151855088 151855088 TGTTCTAAAGATCAGTCCTCGCGCAGTGGCTCAAGGCTGTAATCTCAGCATTTTGGGAGGCCGAG TGTTCTAAAGATCAGTCCTCGCGCAGTGGCTCCAGGCTGTAATCTCAGCATTTTGGGAGGCCGAG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1413145200 Functional Loss SNV dbSNP153 33..33 33 - - - 36843 RMVar_ID_36843 Human_SNP_ID_33772458 A-to-I Human chr1 - 151871267 151871267 151871267 GGGCTGGAATGCAGAGACACAATCTCAGCTCAATGCAACCTCCACCTCCCAGGTTCAAGCGATTC GGGCTGGAATGCAGAGACACAATCTCAGCTCAGTGCAACCTCCACCTCCCAGGTTCAAGCGATTC T C THEM4 Ensembl:ENSG00000159445 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs147007922 Functional Loss SNV dbSNP153 33..33 33 - - - 36844 RMVar_ID_36844 Human_SNP_ID_33773190 A-to-I Human chr1 - 151874467 151874467 151874467 AGGAGGCTGAGGCAGGAGAATTGCTTGAACCCAGGAGGAAGAGGTTGCAGTGAGCCAAGATCATG AGGAGGCTGAGGCAGGAGAATTGCTTGAACCCCGGAGGAAGAGGTTGCAGTGAGCCAAGATCATG T G THEM4 Ensembl:ENSG00000159445 Protein coding 3'UTR GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs570331421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1458 36845 RMVar_ID_36845 Human_SNP_ID_33777503 A-to-I Human chr1 - 151893154 151893151 151893155 TTGGCCGGGCTGGTCTCGAACTCCTAAATTCAAGTGATCTGCCCCACCTTGGCCTCCCAAAGTGC TTGGCCGGGCTGGTCTCGAACTCCTAAATTC____GATCTGCCCCACCTTGGCCTCCCAAAGTGC CACTT C THEM4 Ensembl:ENSG00000159445 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277583877 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_24588527 RMVar_hsa_circ_369425,RMVar_hsa_circ_136175,RMVar_hsa_circ_104150,RMVar_hsa_circ_136177 36846 RMVar_ID_36846 Human_SNP_ID_33777513 A-to-I Human chr1 - 151893189 151893189 151893189 TTTTATATTTTTAATAGAGACAGGGTTTCACAATGTTGGCCGGGCTGGTCTCGAACTCCTAAATT TTTTATATTTTTAATAGAGACAGGGTTTCACAGTGTTGGCCGGGCTGGTCTCGAACTCCTAAATT T C THEM4 Ensembl:ENSG00000159445 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971393765 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_369425,RMVar_hsa_circ_136175,RMVar_hsa_circ_104150,RMVar_hsa_circ_136177 36847 RMVar_ID_36847 Human_SNP_ID_34113769 A-to-I Human chr1 + 153183199 153183199 153183199 CAAGCGATTCTTTAAATTATGTGTGGTGGCGCATGCCTGTAATCCCAAGTAGCTGGGATTACAGG CAAGCGATTCTTTAAATTATGTGTGGTGGCGCGTGCCTGTAATCCCAAGTAGCTGGGATTACAGG A G AL161636.1 Ensembl:ENSG00000229699 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1007014086 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9555099,Human_RBP_ID_11183852,Human_RBP_ID_22847016,Human_RBP_ID_24588663 36848 RMVar_ID_36848 Human_SNP_ID_34222175 A-to-I Human chr1 - 153605768 153605768 153605768 TGCTTCAAAAAAATGAAAACTCCAGCCTGACCAACATGTAGAAACCCCGTCTCTACTAAAAATAC TGCTTCAAAAAAATGAAAACTCCAGCCTGACCTACATGTAGAAACCCCGTCTCTACTAAAAATAC T A BX470102.2 Ensembl:ENSG00000285867 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs763619509 Functional Loss SNV dbSNP153 33..33 33 - - - 36849 RMVar_ID_36849 Human_SNP_ID_34226124 A-to-I Human chr1 - 153620248 153620248 153620248 GAGTCCCACTCTGTAGCCCAGACTGGAGTGCAATGGCGCGATCTCTGCTCACCACAACCTCCGCC GAGTCCCACTCTGTAGCCCAGACTGGAGTGCAGTGGCGCGATCTCTGCTCACCACAACCTCCGCC T C S100A13 Ensembl:ENSG00000189171 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs897807215 Functional Loss SNV dbSNP153 33..33 33 - - - 36850 RMVar_ID_36850 Human_SNP_ID_34226406 A-to-I Human chr1 - 153621529 153621529 153621529 ACCTCGAGTTATCCACCCGCCTTGGCCTCCCAAAGTTCTGGGATTACAGGCATGAGCCACCATGC ACCTCGAGTTATCCACCCGCCTTGGCCTCCCAGAGTTCTGGGATTACAGGCATGAGCCACCATGC T C S100A13 Ensembl:ENSG00000189171 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1205960990 Functional Loss SNV dbSNP153 33..33 33 - - - 36851 RMVar_ID_36851 Human_SNP_ID_34226771 A-to-I Human chr1 - 153623021 153623021 153623021 CAATGGCGTGATTACAGTTCACTGCAGCCTCTACCTCCTACGCTCAAGTGATCCTTCCACCTCAG CAATGGCGTGATTACAGTTCACTGCAGCCTCTGCCTCCTACGCTCAAGTGATCCTTCCACCTCAG T C S100A13 Ensembl:ENSG00000189171 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs894538275 Functional Loss SNV dbSNP153 33..33 33 - - - 36852 RMVar_ID_36852 Human_SNP_ID_34230262 A-to-I Human chr1 + 153635111 153635111 153635111 ACCTCAGGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGAAAACAGGCGTGAGCCACCGCGC ACCTCAGGTGATCCGCCCGCCTCGGCCTCCCACAGTGCTGGGAAAACAGGCGTGAGCCACCGCGC A C CHTOP Ensembl:ENSG00000160679 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs182244942 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136223,RMVar_hsa_circ_87326 36853 RMVar_ID_36853 Human_SNP_ID_34230263 A-to-I Human chr1 + 153635111 153635111 153635111 ACCTCAGGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGAAAACAGGCGTGAGCCACCGCGC ACCTCAGGTGATCCGCCCGCCTCGGCCTCCCAGAGTGCTGGGAAAACAGGCGTGAGCCACCGCGC A G CHTOP Ensembl:ENSG00000160679 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs182244942 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136223,RMVar_hsa_circ_87326 36854 RMVar_ID_36854 Human_SNP_ID_34230364 A-to-I Human chr1 + 153635426 153635426 153635426 CTCCCGCCTTGGCCTCCCAAAGTGCTGAGATTACAGGCGTGAAGCACCGCGCCCGCCCTGTCCGG CTCCCGCCTTGGCCTCCCAAAGTGCTGAGATTGCAGGCGTGAAGCACCGCGCCCGCCCTGTCCGG A G CHTOP Ensembl:ENSG00000160679 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1161987663 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136223,RMVar_hsa_circ_87326 36855 RMVar_ID_36855 Human_SNP_ID_34231360 A-to-I Human chr1 + 153638955 153638955 153638955 CAGGCTGGAGTGCAGTGGCACGATCTCGGCTCACTGCAAGCTCCGCCTCCCGGGTCCATACCATT CAGGCTGGAGTGCAGTGGCACGATCTCGGCTCCCTGCAAGCTCCGCCTCCCGGGTCCATACCATT A C CHTOP Ensembl:ENSG00000160679 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900138357 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10583263 RMVar_hsa_circ_136223,RMVar_hsa_circ_87326 36856 RMVar_ID_36856 Human_SNP_ID_34231361 A-to-I Human chr1 + 153638955 153638955 153638955 CAGGCTGGAGTGCAGTGGCACGATCTCGGCTCACTGCAAGCTCCGCCTCCCGGGTCCATACCATT CAGGCTGGAGTGCAGTGGCACGATCTCGGCTCGCTGCAAGCTCCGCCTCCCGGGTCCATACCATT A G CHTOP Ensembl:ENSG00000160679 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900138357 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10583263 RMVar_hsa_circ_136223,RMVar_hsa_circ_87326 36857 RMVar_ID_36857 Human_SNP_ID_34231362 A-to-I Human chr1 + 153638955 153638955 153638955 CAGGCTGGAGTGCAGTGGCACGATCTCGGCTCACTGCAAGCTCCGCCTCCCGGGTCCATACCATT CAGGCTGGAGTGCAGTGGCACGATCTCGGCTCTCTGCAAGCTCCGCCTCCCGGGTCCATACCATT A T CHTOP Ensembl:ENSG00000160679 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900138357 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10583263 RMVar_hsa_circ_136223,RMVar_hsa_circ_87326 36858 RMVar_ID_36858 Human_SNP_ID_34231429 A-to-I Human chr1 + 153639142 153639142 153639142 TGACCTCGTGATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCTTGAGCCACCGCGC TGACCTCGTGATCCACCCGCCTCGGCCTCCCAGAGTGCTGGGATTACAGGCTTGAGCCACCGCGC A G CHTOP Ensembl:ENSG00000160679 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1054046231 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24588800 RMVar_hsa_circ_136223,RMVar_hsa_circ_87326 36859 RMVar_ID_36859 Human_SNP_ID_34231667 A-to-I Human chr1 + 153640026 153640026 153640026 GAACTCCTGACCTCAAGTGATCTGCCTGCCTCAGTATCCCAAAGTGTTCAGATTACAGGCATGAG GAACTCCTGACCTCAAGTGATCTGCCTGCCTCGGTATCCCAAAGTGTTCAGATTACAGGCATGAG A G CHTOP Ensembl:ENSG00000160679 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1432550027 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136223,RMVar_hsa_circ_87326 36860 RMVar_ID_36860 Human_SNP_ID_34231719 A-to-I Human chr1 + 153640241 153640241 153640241 CCAGGCCTGTAATCCCAGCACTCTGGGAGGCCAAGGCAGGCGGATCACTTGAGGTCAGGAGTTTG CCAGGCCTGTAATCCCAGCACTCTGGGAGGCCGAGGCAGGCGGATCACTTGAGGTCAGGAGTTTG A G CHTOP Ensembl:ENSG00000160679 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1265800107 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23302838 RMVar_hsa_circ_136223,RMVar_hsa_circ_87326 36861 RMVar_ID_36861 Human_SNP_ID_34231730 A-to-I Human chr1 + 153640296 153640296 153640296 CAGGAGTTTGAGACTAGCCTGGCCAATGTGGCAAAACCCCATCTCTACTAAAAAAAAAAAAAAGC CAGGAGTTTGAGACTAGCCTGGCCAATGTGGCGAAACCCCATCTCTACTAAAAAAAAAAAAAAGC A G CHTOP Ensembl:ENSG00000160679 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs911130865 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136223,RMVar_hsa_circ_87326 36862 RMVar_ID_36862 Human_SNP_ID_34231817 A-to-I Human chr1 + 153640578 153640578 153640578 TGGGCAGGTGGATCACCTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGACAAGACCCCGT TGGGCAGGTGGATCACCTGAGGTCAGGAGTTCCAGACCAGCCTGGCCAACATGACAAGACCCCGT A C CHTOP Ensembl:ENSG00000160679 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1315917208 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10583346,Human_RBP_ID_24588831 RMVar_hsa_circ_136223,RMVar_hsa_circ_87326 36863 RMVar_ID_36863 Human_SNP_ID_34231829 A-to-I Human chr1 + 153640624 153640624 153640624 CAACATGACAAGACCCCGTCTCCACCAAAAATAAGCCAGGCGTGATGACAGCTCCTGTAATCCCA CAACATGACAAGACCCCGTCTCCACCAAAAATGAGCCAGGCGTGATGACAGCTCCTGTAATCCCA A G CHTOP Ensembl:ENSG00000160679 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947421643 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10583348 RMVar_hsa_circ_136223,RMVar_hsa_circ_87326 36864 RMVar_ID_36864 Human_SNP_ID_34231831 A-to-I Human chr1 + 153640629 153640629 153640629 TGACAAGACCCCGTCTCCACCAAAAATAAGCCAGGCGTGATGACAGCTCCTGTAATCCCAGCTAC TGACAAGACCCCGTCTCCACCAAAAATAAGCCGGGCGTGATGACAGCTCCTGTAATCCCAGCTAC A G CHTOP Ensembl:ENSG00000160679 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1043054107 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10583349,Human_RBP_ID_24588833 RMVar_hsa_circ_136223,RMVar_hsa_circ_87326 36865 RMVar_ID_36865 Human_SNP_ID_34231832 A-to-I Human chr1 + 153640629 153640629 153640629 TGACAAGACCCCGTCTCCACCAAAAATAAGCCAGGCGTGATGACAGCTCCTGTAATCCCAGCTAC TGACAAGACCCCGTCTCCACCAAAAATAAGCCTGGCGTGATGACAGCTCCTGTAATCCCAGCTAC A T CHTOP Ensembl:ENSG00000160679 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1043054107 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10583349,Human_RBP_ID_24588833 RMVar_hsa_circ_136223,RMVar_hsa_circ_87326 36866 RMVar_ID_36866 Human_SNP_ID_34231846 A-to-I Human chr1 + 153640682 153640682 153640682 AATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGTTTGAACCTGGGAGACGAAGGTTGCAGT AATCCCAGCTACTCGGGAGGCTGAGGCAGGAGGATTGTTTGAACCTGGGAGACGAAGGTTGCAGT A G CHTOP Ensembl:ENSG00000160679 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006566870 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136223,RMVar_hsa_circ_87326 36867 RMVar_ID_36867 Human_SNP_ID_34233792 A-to-I Human chr1 + 153647740 153647740 153647740 ACAGTGCTAAAAGAACACCTGAGGCTGGGCACAGTGGCTTACGCCTGTAATCCCAGCACTTTGGG ACAGTGCTAAAAGAACACCTGAGGCTGGGCACGGTGGCTTACGCCTGTAATCCCAGCACTTTGGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270210130 Functional Loss SNV dbSNP153 33..33 33 - - - 36868 RMVar_ID_36868 Human_SNP_ID_34237650 A-to-I Human chr1 + 153661910 153661907 153661911 TTAATTCAAAGACAGCTTCAAATTGTGATCTGAGTATTTATAATTAAATGACTCAATTATCATTT TTAATTCAAAGACAGCTTCAAATTGTGATC____TATTTATAATTAAATGACTCAATTATCATTT CTGAG C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1319605801 Functional Loss DEL dbSNP153 31..34 33 - - - 36869 RMVar_ID_36869 Human_SNP_ID_34237786 A-to-I Human chr1 + 153662377 153662377 153662377 AGCTTAGGCTCCAGTCTTCCCCCTTGGGTAGGAAAAGGAGTGAAGGGAATGTCACTCCTGAGTTT AGCTTAGGCTCCAGTCTTCCCCCTTGGGTAGGGAAAGGAGTGAAGGGAATGTCACTCCTGAGTTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1130607 Functional Loss SNV dbSNP153 33..33 33 - - - 36870 RMVar_ID_36870 Human_SNP_ID_34238851 A-to-I Human chr1 - 153666321 153666321 153666321 AAATTAGCCAGGCGTGGTGGTGGGCGTCTGTAATCCCCACTACTTGGGAGGCTGAGGCAGGAGAG AAATTAGCCAGGCGTGGTGGTGGGCGTCTGTAGTCCCCACTACTTGGGAGGCTGAGGCAGGAGAG T C ILF2 Ensembl:ENSG00000143621 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1271001392 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136227,RMVar_hsa_circ_104995,RMVar_hsa_circ_126664,RMVar_hsa_circ_120297,RMVar_hsa_circ_95774,RMVar_hsa_circ_94614,RMVar_hsa_circ_136231,RMVar_hsa_circ_84560,RMVar_hsa_circ_136229,RMVar_hsa_circ_136230,RMVar_hsa_circ_136228,RMVar_hsa_circ_26670,RMVar_hsa_circ_123443,RMVar_hsa_circ_136226,RMVar_hsa_circ_108615,RMVar_hsa_circ_136240,RMVar_hsa_circ_82146,RMVar_hsa_circ_136242,RMVar_hsa_circ_106661,RMVar_hsa_circ_127208,RMVar_hsa_circ_91645,RMVar_hsa_circ_136244,RMVar_hsa_circ_136246,RMVar_hsa_circ_136245,RMVar_hsa_circ_97045,RMVar_hsa_circ_308802,RMVar_hsa_circ_136243,RMVar_hsa_circ_136253,RMVar_hsa_circ_136254,RMVar_hsa_circ_78949,RMVar_hsa_circ_136257,RMVar_hsa_circ_65490,RMVar_hsa_circ_279877,RMVar_hsa_circ_136258,RMVar_hsa_circ_115795,RMVar_hsa_circ_136262 36871 RMVar_ID_36871 Human_SNP_ID_34238852 A-to-I Human chr1 - 153666322 153666322 153666322 AAAATTAGCCAGGCGTGGTGGTGGGCGTCTGTAATCCCCACTACTTGGGAGGCTGAGGCAGGAGA AAAATTAGCCAGGCGTGGTGGTGGGCGTCTGTGATCCCCACTACTTGGGAGGCTGAGGCAGGAGA T C ILF2 Ensembl:ENSG00000143621 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1052556273 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136227,RMVar_hsa_circ_104995,RMVar_hsa_circ_126664,RMVar_hsa_circ_120297,RMVar_hsa_circ_95774,RMVar_hsa_circ_94614,RMVar_hsa_circ_136231,RMVar_hsa_circ_84560,RMVar_hsa_circ_136229,RMVar_hsa_circ_136230,RMVar_hsa_circ_136228,RMVar_hsa_circ_26670,RMVar_hsa_circ_123443,RMVar_hsa_circ_136226,RMVar_hsa_circ_108615,RMVar_hsa_circ_136240,RMVar_hsa_circ_82146,RMVar_hsa_circ_136242,RMVar_hsa_circ_106661,RMVar_hsa_circ_127208,RMVar_hsa_circ_91645,RMVar_hsa_circ_136244,RMVar_hsa_circ_136246,RMVar_hsa_circ_136245,RMVar_hsa_circ_97045,RMVar_hsa_circ_308802,RMVar_hsa_circ_136243,RMVar_hsa_circ_136253,RMVar_hsa_circ_136254,RMVar_hsa_circ_78949,RMVar_hsa_circ_136257,RMVar_hsa_circ_65490,RMVar_hsa_circ_279877,RMVar_hsa_circ_136258,RMVar_hsa_circ_115795,RMVar_hsa_circ_136262 36872 RMVar_ID_36872 Human_SNP_ID_34239506 A-to-I Human chr1 - 153669039 153669039 153669039 ATGCCCAGCTAATTTTTGTATGTCTGTTTAGTAGAGACGGGGTTTCACCATGTTGCCCAGGCTGA ATGCCCAGCTAATTTTTGTATGTCTGTTTAGTGGAGACGGGGTTTCACCATGTTGCCCAGGCTGA T C ILF2 Ensembl:ENSG00000143621 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1191474646 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136227,RMVar_hsa_circ_120297,RMVar_hsa_circ_84560,RMVar_hsa_circ_136226,RMVar_hsa_circ_108615,RMVar_hsa_circ_82146,RMVar_hsa_circ_136242,RMVar_hsa_circ_106661,RMVar_hsa_circ_136244,RMVar_hsa_circ_97045,RMVar_hsa_circ_136243,RMVar_hsa_circ_136254,RMVar_hsa_circ_78949,RMVar_hsa_circ_136257,RMVar_hsa_circ_37248,RMVar_hsa_circ_136264,RMVar_hsa_circ_312449 36873 RMVar_ID_36873 Human_SNP_ID_34245938 A-to-I Human chr1 + 153690875 153690875 153690875 TGAGGCAGAAGAATTGCTTGAACCCGGGAGGCAGAGGTTGCGATGAGCCAAGATTACACCACGCA TGAGGCAGAAGAATTGCTTGAACCCGGGAGGCCGAGGTTGCGATGAGCCAAGATTACACCACGCA A C NPR1 Ensembl:ENSG00000169418 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1359296685 Functional Loss SNV dbSNP153 33..33 33 - - - 36874 RMVar_ID_36874 Human_SNP_ID_34262807 A-to-I Human chr1 + 153753855 153753855 153753855 ATGTTGTATTTTTGTAGAGATGGAGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGACCT ATGTTGTATTTTTGTAGAGATGGAGTTTCACCGTGTTGGCCAGGCTGGTCTTGAACTCCTGACCT A G INTS3 Ensembl:ENSG00000143624 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs779670726 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48593,RMVar_hsa_circ_113049,RMVar_hsa_circ_136268,RMVar_hsa_circ_24292,RMVar_hsa_circ_344007,RMVar_hsa_circ_105743,RMVar_hsa_circ_98446,RMVar_hsa_circ_375720,RMVar_hsa_circ_136272,RMVar_hsa_circ_120592,RMVar_hsa_circ_136273,RMVar_hsa_circ_318009,RMVar_hsa_circ_337531,RMVar_hsa_circ_109589,RMVar_hsa_circ_136274,RMVar_hsa_circ_347928,RMVar_hsa_circ_136275,RMVar_hsa_circ_293110,RMVar_hsa_circ_136277,RMVar_hsa_circ_136279,RMVar_hsa_circ_96334,RMVar_hsa_circ_136278,RMVar_hsa_circ_136276,RMVar_hsa_circ_289942,RMVar_hsa_circ_8493,RMVar_hsa_circ_24624,RMVar_hsa_circ_136280,RMVar_hsa_circ_136281,RMVar_hsa_circ_136282,RMVar_hsa_circ_136283,RMVar_hsa_circ_115117 36875 RMVar_ID_36875 Human_SNP_ID_34262858 A-to-I Human chr1 + 153754001 153754001 153754001 TTTTTTTCTGTTTTTTAAGATGGGGTGTCACCATGTTGCCAAGGCTGGTCTTGAACTCGTAGGCT TTTTTTTCTGTTTTTTAAGATGGGGTGTCACCCTGTTGCCAAGGCTGGTCTTGAACTCGTAGGCT A C INTS3 Ensembl:ENSG00000143624 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1224769090 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48593,RMVar_hsa_circ_113049,RMVar_hsa_circ_136268,RMVar_hsa_circ_24292,RMVar_hsa_circ_344007,RMVar_hsa_circ_105743,RMVar_hsa_circ_98446,RMVar_hsa_circ_375720,RMVar_hsa_circ_136272,RMVar_hsa_circ_120592,RMVar_hsa_circ_136273,RMVar_hsa_circ_318009,RMVar_hsa_circ_337531,RMVar_hsa_circ_109589,RMVar_hsa_circ_136274,RMVar_hsa_circ_347928,RMVar_hsa_circ_136275,RMVar_hsa_circ_293110,RMVar_hsa_circ_136277,RMVar_hsa_circ_136279,RMVar_hsa_circ_96334,RMVar_hsa_circ_136278,RMVar_hsa_circ_136276,RMVar_hsa_circ_289942,RMVar_hsa_circ_8493,RMVar_hsa_circ_24624,RMVar_hsa_circ_136280,RMVar_hsa_circ_136281,RMVar_hsa_circ_136282,RMVar_hsa_circ_136283,RMVar_hsa_circ_115117 36876 RMVar_ID_36876 Human_SNP_ID_34262872 A-to-I Human chr1 + 153754075 153754075 153754075 CACCTGCCTCGGCCTCCCAAGGTGCTAGGATTACAGGTGTGAGCCACCATGCTGGTCTTTTAAAT CACCTGCCTCGGCCTCCCAAGGTGCTAGGATTCCAGGTGTGAGCCACCATGCTGGTCTTTTAAAT A C INTS3 Ensembl:ENSG00000143624 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1394940701 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48593,RMVar_hsa_circ_113049,RMVar_hsa_circ_136268,RMVar_hsa_circ_24292,RMVar_hsa_circ_344007,RMVar_hsa_circ_105743,RMVar_hsa_circ_98446,RMVar_hsa_circ_375720,RMVar_hsa_circ_136272,RMVar_hsa_circ_120592,RMVar_hsa_circ_136273,RMVar_hsa_circ_318009,RMVar_hsa_circ_337531,RMVar_hsa_circ_109589,RMVar_hsa_circ_136274,RMVar_hsa_circ_347928,RMVar_hsa_circ_136275,RMVar_hsa_circ_293110,RMVar_hsa_circ_136277,RMVar_hsa_circ_136279,RMVar_hsa_circ_96334,RMVar_hsa_circ_136278,RMVar_hsa_circ_136276,RMVar_hsa_circ_289942,RMVar_hsa_circ_8493,RMVar_hsa_circ_24624,RMVar_hsa_circ_136280,RMVar_hsa_circ_136281,RMVar_hsa_circ_136282,RMVar_hsa_circ_136283,RMVar_hsa_circ_115117 36877 RMVar_ID_36877 Human_SNP_ID_34263363 A-to-I Human chr1 + 153756166 153756166 153756166 GGAGGCTGAGGCTGGTGGGAACACTTGAGGTCAGGAGTTCAAGACTAGCCGGGCAACATGATGAA GGAGGCTGAGGCTGGTGGGAACACTTGAGGTCGGGAGTTCAAGACTAGCCGGGCAACATGATGAA A G INTS3 Ensembl:ENSG00000143624 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs150676131 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48593,RMVar_hsa_circ_113049,RMVar_hsa_circ_136268,RMVar_hsa_circ_24292,RMVar_hsa_circ_344007,RMVar_hsa_circ_105743,RMVar_hsa_circ_98446,RMVar_hsa_circ_375720,RMVar_hsa_circ_136272,RMVar_hsa_circ_120592,RMVar_hsa_circ_136273,RMVar_hsa_circ_318009,RMVar_hsa_circ_337531,RMVar_hsa_circ_109589,RMVar_hsa_circ_136274,RMVar_hsa_circ_136275,RMVar_hsa_circ_293110,RMVar_hsa_circ_136277,RMVar_hsa_circ_136279,RMVar_hsa_circ_96334,RMVar_hsa_circ_136278,RMVar_hsa_circ_289942,RMVar_hsa_circ_116662,RMVar_hsa_circ_8493,RMVar_hsa_circ_24624,RMVar_hsa_circ_136280,RMVar_hsa_circ_136281,RMVar_hsa_circ_136282,RMVar_hsa_circ_136283,RMVar_hsa_circ_115117,RMVar_hsa_circ_293052,RMVar_hsa_circ_96391,RMVar_hsa_circ_136285,RMVar_hsa_circ_136287,RMVar_hsa_circ_38268,RMVar_hsa_circ_136286 36878 RMVar_ID_36878 Human_SNP_ID_34281081 A-to-I Human chr1 - 153821179 153821179 153821179 AGGAATTCAAGACTAGCCTGGGCAGCATAGCAAGACCCCCACCCCTTACAAAAAAATAAAAAATT AGGAATTCAAGACTAGCCTGGGCAGCATAGCAGGACCCCCACCCCTTACAAAAAAATAAAAAATT T C GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350328136 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32482,RMVar_hsa_circ_356213,RMVar_hsa_circ_344971,RMVar_hsa_circ_46063,RMVar_hsa_circ_360643 36879 RMVar_ID_36879 Human_SNP_ID_34281297 A-to-I Human chr1 - 153822134 153822134 153822134 CTCTGTCACCCAGGCTGGAGTGTAGTGGTGCAATCTCGGCTCATTGCAACCTCCACCTCCCAGGT CTCTGTCACCCAGGCTGGAGTGTAGTGGTGCAGTCTCGGCTCATTGCAACCTCCACCTCCCAGGT T C GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs898515907 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32482,RMVar_hsa_circ_356213,RMVar_hsa_circ_344971,RMVar_hsa_circ_46063,RMVar_hsa_circ_360643 36880 RMVar_ID_36880 Human_SNP_ID_34281425 A-to-I Human chr1 - 153822589 153822589 153822589 AGGAGAATCACTTAAACCTGAGAGGAGGTTGCAGTGCGCCGAGATTGCACCATTGCCCTCCAGCC AGGAGAATCACTTAAACCTGAGAGGAGGTTGCGGTGCGCCGAGATTGCACCATTGCCCTCCAGCC T C GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1411338360 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32482,RMVar_hsa_circ_356213,RMVar_hsa_circ_344971,RMVar_hsa_circ_46063,RMVar_hsa_circ_360643 36881 RMVar_ID_36881 Human_SNP_ID_34281870 A-to-I Human chr1 - 153824254 153824254 153824254 ATGAGGTGTTGCTGTGTTGCCCAGGCTGACGTACATTGGCTGTTCACAAGCACTGTCATAGTGCA ATGAGGTGTTGCTGTGTTGCCCAGGCTGACGTGCATTGGCTGTTCACAAGCACTGTCATAGTGCA T C GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs75860520 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32482,RMVar_hsa_circ_356213,RMVar_hsa_circ_344971,RMVar_hsa_circ_46063,RMVar_hsa_circ_360643 36882 RMVar_ID_36882 Human_SNP_ID_34282226 A-to-I Human chr1 - 153825470 153825470 153825470 GCAGTGAGCTGAGATCGTGCCACTGCACTCCAACCTGGGCAACAGAGTGAGACTCTTGTCTCCAT GCAGTGAGCTGAGATCGTGCCACTGCACTCCAGCCTGGGCAACAGAGTGAGACTCTTGTCTCCAT T C GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs948112320 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_610 RMVar_hsa_circ_32482,RMVar_hsa_circ_356213,RMVar_hsa_circ_344971,RMVar_hsa_circ_46063,RMVar_hsa_circ_360643 36883 RMVar_ID_36883 Human_SNP_ID_34282401 A-to-I Human chr1 - 153826142 153826142 153826142 AAAATTTGCCAGGCATGGTGGCAGGTGCCTGTAGTCCCCGCTACTTGGGAGGCTGAGGCAGGAGA AAAATTTGCCAGGCATGGTGGCAGGTGCCTGTGGTCCCCGCTACTTGGGAGGCTGAGGCAGGAGA T C GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1557787681 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32482,RMVar_hsa_circ_356213,RMVar_hsa_circ_344971,RMVar_hsa_circ_46063,RMVar_hsa_circ_360643 36884 RMVar_ID_36884 Human_SNP_ID_34282505 A-to-I Human chr1 - 153826466 153826466 153826466 GTGCCTGCACACCCAGCTAGTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGGTAGCCCGGC GTGCCTGCACACCCAGCTAGTTTTGTATTTTTGGTAGAGATGGGGTTTCACCATGGTAGCCCGGC T C GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs948583631 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32482,RMVar_hsa_circ_356213,RMVar_hsa_circ_344971,RMVar_hsa_circ_46063,RMVar_hsa_circ_360643 36885 RMVar_ID_36885 Human_SNP_ID_34282570 A-to-I Human chr1 - 153826722 153826722 153826722 TTGCCCAGGCTGGTCTCAAACTCTCAGCCTCAAGTGATCTTCCCACATTGGCCTCCCAAAGTGCT TTGCCCAGGCTGGTCTCAAACTCTCAGCCTCAGGTGATCTTCCCACATTGGCCTCCCAAAGTGCT T C GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277379947 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32482,RMVar_hsa_circ_356213,RMVar_hsa_circ_344971,RMVar_hsa_circ_46063,RMVar_hsa_circ_360643 36886 RMVar_ID_36886 Human_SNP_ID_34285327 A-to-I Human chr1 - 153837294 153837294 153837294 AGATAAGGGCATCTTACTCTGTTGCCTAGGCTAGTCTTCAACTCCTGACACTCAAGCATTCCTCC AGATAAGGGCATCTTACTCTGTTGCCTAGGCTGGTCTTCAACTCCTGACACTCAAGCATTCCTCC T C GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs758173878 Functional Loss SNV dbSNP153 33..33 33 - - - 36887 RMVar_ID_36887 Human_SNP_ID_34288771 A-to-I Human chr1 - 153849693 153849693 153849693 CCGGAAGGAGGGGGTTGCAGTGAGCCAAGATCACGCCACTGTACTGCAGCCTGGGTGAAAGAGTG CCGGAAGGAGGGGGTTGCAGTGAGCCAAGATCGCGCCACTGTACTGCAGCCTGGGTGAAAGAGTG T C GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs572065630 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9457891,Human_RBP_ID_24589606 36888 RMVar_ID_36888 Human_SNP_ID_34288987 A-to-I Human chr1 - 153850499 153850499 153850499 GGTCAGGAGTTCGAGACCACCCTCGCCAACATAGTGATACCTGGTCTCTACTGAAAATACAAAAA GGTCAGGAGTTCGAGACCACCCTCGCCAACATGGTGATACCTGGTCTCTACTGAAAATACAAAAA T C GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910019786 Functional Loss SNV dbSNP153 33..33 33 - - - 36889 RMVar_ID_36889 Human_SNP_ID_34291047 A-to-I Human chr1 - 153858422 153858422 153858422 TTTTCTATTTTTTGTAGAGATGGGGCTTTGCCATGTTGCCTAGGCTGGTCTTGAACTCGTGTTTT TTTTCTATTTTTTGTAGAGATGGGGCTTTGCCGTGTTGCCTAGGCTGGTCTTGAACTCGTGTTTT T C GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1424359303 Functional Loss SNV dbSNP153 33..33 33 - - - 36890 RMVar_ID_36890 Human_SNP_ID_34291071 A-to-I Human chr1 - 153858510 153858510 153858510 GCCTTGACCTCCTGAGCTCAAGCGATCCTCCCACCTCAGCCTCCTGGGTAGCTGGGACCGCAGGT GCCTTGACCTCCTGAGCTCAAGCGATCCTCCCTCCTCAGCCTCCTGGGTAGCTGGGACCGCAGGT T A GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs562361210 Functional Loss SNV dbSNP153 33..33 33 - - - 36891 RMVar_ID_36891 Human_SNP_ID_34291254 A-to-I Human chr1 - 153859284 153859261 153859285 TGGCTCACTACAGACTAGATCCCCCAGGCTCAAGCAATCCTCCCACCCCAGCCTCCTGAGTAGCT TGGCTCACTACAGACTAGATCCCCCAGGCTC________________________CTGAGTAGCT GGAGGCTGGGGTGGGAGGATTGCTT G GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017863825 Functional Loss DEL dbSNP153 32..55 33 - - - 36892 RMVar_ID_36892 Human_SNP_ID_34293001 A-to-I Human chr1 - 153864926 153864926 153864926 AGCTGGGACTACAGGCACACGCCACTGTGCCCAGCTGATTTTTTGTGTTTTTAGTGGAGACAGGG AGCTGGGACTACAGGCACACGCCACTGTGCCCGGCTGATTTTTTGTGTTTTTAGTGGAGACAGGG T C GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1312032277 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8285768 36893 RMVar_ID_36893 Human_SNP_ID_34294000 A-to-I Human chr1 - 153868803 153868803 153868803 TTGAACCCAGGAGGGGAGGCTGCAGTGAGCCAAGATGGTGCCACTGCACTCCACCCTGGGTGACG TTGAACCCAGGAGGGGAGGCTGCAGTGAGCCAGGATGGTGCCACTGCACTCCACCCTGGGTGACG T C GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1421962390 Functional Loss SNV dbSNP153 33..33 33 - - - 36894 RMVar_ID_36894 Human_SNP_ID_34294003 A-to-I Human chr1 - 153868808 153868808 153868808 ATGGCTTGAACCCAGGAGGGGAGGCTGCAGTGAGCCAAGATGGTGCCACTGCACTCCACCCTGGG ATGGCTTGAACCCAGGAGGGGAGGCTGCAGTGCGCCAAGATGGTGCCACTGCACTCCACCCTGGG T G GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1014256659 Functional Loss SNV dbSNP153 33..33 33 - - - 36895 RMVar_ID_36895 Human_SNP_ID_34294010 A-to-I Human chr1 - 153868827 153868827 153868827 GGGAGGCTGAGGCAGGAGAATGGCTTGAACCCAGGAGGGGAGGCTGCAGTGAGCCAAGATGGTGC GGGAGGCTGAGGCAGGAGAATGGCTTGAACCCTGGAGGGGAGGCTGCAGTGAGCCAAGATGGTGC T A GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs970032233 Functional Loss SNV dbSNP153 33..33 33 - - - 36896 RMVar_ID_36896 Human_SNP_ID_34294100 A-to-I Human chr1 - 153869170 153869170 153869170 CTTCCGGCTCAGCCTCTCAAGTAGCTGGGACTACAGGCACCCACCATCATGCCTGGCTAACTTTT CTTCCGGCTCAGCCTCTCAAGTAGCTGGGACTGCAGGCACCCACCATCATGCCTGGCTAACTTTT T C GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1409680307 Functional Loss SNV dbSNP153 33..33 33 - - - 36897 RMVar_ID_36897 Human_SNP_ID_34294102 A-to-I Human chr1 - 153869180 153869180 153869180 TCAAGTGATTCTTCCGGCTCAGCCTCTCAAGTAGCTGGGACTACAGGCACCCACCATCATGCCTG TCAAGTGATTCTTCCGGCTCAGCCTCTCAAGTGGCTGGGACTACAGGCACCCACCATCATGCCTG T C GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs936149247 Functional Loss SNV dbSNP153 33..33 33 - - - 36898 RMVar_ID_36898 Human_SNP_ID_34294105 A-to-I Human chr1 - 153869184 153869184 153869184 GGGTTCAAGTGATTCTTCCGGCTCAGCCTCTCAAGTAGCTGGGACTACAGGCACCCACCATCATG GGGTTCAAGTGATTCTTCCGGCTCAGCCTCTCCAGTAGCTGGGACTACAGGCACCCACCATCATG T G GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1170061040 Functional Loss SNV dbSNP153 33..33 33 - - - 36899 RMVar_ID_36899 Human_SNP_ID_34294356 A-to-I Human chr1 - 153870222 153870222 153870222 AGGGTGACCAGGTACAGTGGCTCATGCTTGCAATCCCAGCACTTTGGAGGCCGAGGCAGGTGGAT AGGGTGACCAGGTACAGTGGCTCATGCTTGCACTCCCAGCACTTTGGAGGCCGAGGCAGGTGGAT T G GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1478469373 Functional Loss SNV dbSNP153 33..33 33 - - - 36900 RMVar_ID_36900 Human_SNP_ID_34294616 A-to-I Human chr1 - 153871050 153871050 153871050 AAAAACAAAAAACAAAAAACACCAGGCGTGGTAGCACCCATCTGTAATCCCAGCTACTCCAGAGG AAAAACAAAAAACAAAAAACACCAGGCGTGGTGGCACCCATCTGTAATCCCAGCTACTCCAGAGG T C GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1358787687 Functional Loss SNV dbSNP153 33..33 33 - - - 36901 RMVar_ID_36901 Human_SNP_ID_34295579 A-to-I Human chr1 - 153874844 153874844 153874844 GGCTGGATGTGGTGGCTCACACCTGTAATCTCAGCACTTTGGGGGGCCAAGGCGAGTGGATCACC GGCTGGATGTGGTGGCTCACACCTGTAATCTCGGCACTTTGGGGGGCCAAGGCGAGTGGATCACC T C GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs545826065 Functional Loss SNV dbSNP153 33..33 33 - - - 36902 RMVar_ID_36902 Human_SNP_ID_34295583 A-to-I Human chr1 - 153874856 153874856 153874856 AATAAATAAATAGGCTGGATGTGGTGGCTCACACCTGTAATCTCAGCACTTTGGGGGGCCAAGGC AATAAATAAATAGGCTGGATGTGGTGGCTCACGCCTGTAATCTCAGCACTTTGGGGGGCCAAGGC T C GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1309745558 Functional Loss SNV dbSNP153 33..33 33 - - - 36903 RMVar_ID_36903 Human_SNP_ID_34296542 A-to-I Human chr1 - 153878272 153878272 153878272 ATTAGTCGTGGCATGTGCCTGTGGTCCTAGCTACTCGGGAGGCTGGGGTGGGAGGCTGCAGTGAG ATTAGTCGTGGCATGTGCCTGTGGTCCTAGCTGCTCGGGAGGCTGGGGTGGGAGGCTGCAGTGAG T C GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1401306531 Functional Loss SNV dbSNP153 33..33 33 - - - 36904 RMVar_ID_36904 Human_SNP_ID_34298263 A-to-I Human chr1 - 153884868 153884868 153884868 CGTGTAATCCCAGCTGCTTGGGAGGCTGAGGCAGGAGAATTGCTTCAGCCCGGGAGGCAGAGGTT CGTGTAATCCCAGCTGCTTGGGAGGCTGAGGCGGGAGAATTGCTTCAGCCCGGGAGGCAGAGGTT T C GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256682995 Functional Loss SNV dbSNP153 33..33 33 - - - 36905 RMVar_ID_36905 Human_SNP_ID_34298273 A-to-I Human chr1 - 153884894 153884894 153884894 AAATTAGCTGGGTGTGGTGGCAGGCCCGTGTAATCCCAGCTGCTTGGGAGGCTGAGGCAGGAGAA AAATTAGCTGGGTGTGGTGGCAGGCCCGTGTAGTCCCAGCTGCTTGGGAGGCTGAGGCAGGAGAA T C GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs554891253 Functional Loss SNV dbSNP153 33..33 33 - - - 36906 RMVar_ID_36906 Human_SNP_ID_34298747 A-to-I Human chr1 - 153886716 153886716 153886716 TCTCTACTAAAAATACGAAAAAAAAAAAAATTAGCCGGGCGTGTTGGCAGGCACCTGTAGTCCCA TCTCTACTAAAAATACGAAAAAAAAAAAAATTTGCCGGGCGTGTTGGCAGGCACCTGTAGTCCCA T A GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs575435323 Functional Loss SNV dbSNP153 33..33 33 - - - 36907 RMVar_ID_36907 Human_SNP_ID_34298794 A-to-I Human chr1 - 153886854 153886854 153886854 TGGCTTTTTAAAAAAACAGCTATTTTTCGGCCAGACGCAGTGGCTCATGCCTGTAATCCCAGTGC TGGCTTTTTAAAAAAACAGCTATTTTTCGGCCTGACGCAGTGGCTCATGCCTGTAATCCCAGTGC T A GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs775662781 Functional Loss SNV dbSNP153 33..33 33 - - - 36908 RMVar_ID_36908 Human_SNP_ID_34298795 A-to-I Human chr1 - 153886854 153886854 153886854 TGGCTTTTTAAAAAAACAGCTATTTTTCGGCCAGACGCAGTGGCTCATGCCTGTAATCCCAGTGC TGGCTTTTTAAAAAAACAGCTATTTTTCGGCCGGACGCAGTGGCTCATGCCTGTAATCCCAGTGC T C GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs775662781 Functional Loss SNV dbSNP153 33..33 33 - - - 36909 RMVar_ID_36909 Human_SNP_ID_34299028 A-to-I Human chr1 - 153887904 153887904 153887904 TTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCACGGTGGTTTCCAACTCCTGTCCT TTTTGTATTTTTAGTAGAGACAGGGTTTCACCGTGTTGGCCACGGTGGTTTCCAACTCCTGTCCT T C GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1373792023 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10586319 36910 RMVar_ID_36910 Human_SNP_ID_34299648 A-to-I Human chr1 - 153890109 153890109 153890109 GGAGTGCAATGGCGCGATCTTGGCTCACTGCAACCTCTGCCTCCCGGGTTTAAGTGATTCTTCTG GGAGTGCAATGGCGCGATCTTGGCTCACTGCAGCCTCTGCCTCCCGGGTTTAAGTGATTCTTCTG T C GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs994877770 Functional Loss SNV dbSNP153 33..33 33 - - - 36911 RMVar_ID_36911 Human_SNP_ID_34299959 A-to-I Human chr1 - 153891108 153891108 153891108 GCGATCTCAGCTCACTGCAAACTCCGCCTCCCAGGTTCAAGCAGTTCTCCTTCCTCAGCCTCCTG GCGATCTCAGCTCACTGCAAACTCCGCCTCCCGGGTTCAAGCAGTTCTCCTTCCTCAGCCTCCTG T C GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947553699 Functional Loss SNV dbSNP153 33..33 33 - - - 36912 RMVar_ID_36912 Human_SNP_ID_34300969 A-to-I Human chr1 - 153894352 153894352 153894352 GCGATTTTCTTGCCTCAGCCTCCTGAGTAGCTAGAACTGCAGGCGTGTGCCACCACACCTGGCTA GCGATTTTCTTGCCTCAGCCTCCTGAGTAGCTGGAACTGCAGGCGTGTGCCACCACACCTGGCTA T C GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1413877616 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5484413,Human_RBP_ID_10586602,Human_RBP_ID_24589939 36913 RMVar_ID_36913 Human_SNP_ID_34301726 A-to-I Human chr1 - 153897086 153897086 153897086 GGGTGGAGCCTGCAGTGAGCCGAGATCGTGCCACTGCACTCCAGCCTGGGCGACAGCAACACTCC GGGTGGAGCCTGCAGTGAGCCGAGATCGTGCCGCTGCACTCCAGCCTGGGCGACAGCAACACTCC T C GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1426102854 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22560241 36914 RMVar_ID_36914 Human_SNP_ID_34302183 A-to-I Human chr1 - 153898541 153898541 153898541 TTGTATGTTTAGTAGAGATGGGGTTTCACTGTATTGGCCAGGCTGGTCTCCAACTTCTGGTCTCA TTGTATGTTTAGTAGAGATGGGGTTTCACTGTGTTGGCCAGGCTGGTCTCCAACTTCTGGTCTCA T C GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1026187100 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10586758 36915 RMVar_ID_36915 Human_SNP_ID_34302703 A-to-I Human chr1 - 153900607 153900607 153900607 AGAGGCTAAGGTGGAAGGGTTGATTGAACCCAAGAGGTTGAGGCTGCAGTGAGCTGTGATCTCAC AGAGGCTAAGGTGGAAGGGTTGATTGAACCCAGGAGGTTGAGGCTGCAGTGAGCTGTGATCTCAC T C GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs528568438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23333587 36916 RMVar_ID_36916 Human_SNP_ID_34303253 A-to-I Human chr1 - 153902565 153902564 153902565 CTGTGGTCCCAGCTACACAGGAGGCTGAGGTAAGAGAATCCCTTGAGCCCGGGAGGTTGAGGCTG CTGTGGTCCCAGCTACACAGGAGGCTGAGGTA_GAGAATCCCTTGAGCCCGGGAGGTTGAGGCTG CT C GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1035023831 Functional Loss DEL dbSNP153 33..33 33 - - - 36917 RMVar_ID_36917 Human_SNP_ID_34303264 A-to-I Human chr1 - 153902611 153902611 153902611 TTTACAAAAAATATAAGAAAACTTAGCAGGGTATGGTGGTATGTGCCTGTGGTCCCAGCTACACA TTTACAAAAAATATAAGAAAACTTAGCAGGGTGTGGTGGTATGTGCCTGTGGTCCCAGCTACACA T C GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs759460798 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10586917,Human_RBP_ID_24590007 36918 RMVar_ID_36918 Human_SNP_ID_34303286 A-to-I Human chr1 - 153902729 153902729 153902729 GACTGCAGCTGGGCTTGGTGGCTCACACATGTAATCCTAACACTTTGGGAGGCTGAGGTGGGAGG GACTGCAGCTGGGCTTGGTGGCTCACACATGTTATCCTAACACTTTGGGAGGCTGAGGTGGGAGG T A GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs933781179 Functional Loss SNV dbSNP153 33..33 33 - - - 36919 RMVar_ID_36919 Human_SNP_ID_34303402 A-to-I Human chr1 - 153903155 153903155 153903155 GGAGTGCAGTGGAGCGATCTCGGTTCACTGCAAGCTCCGCCTCCTGGTTTCACTCCATTCTCCTG GGAGTGCAGTGGAGCGATCTCGGTTCACTGCAGGCTCCGCCTCCTGGTTTCACTCCATTCTCCTG T C GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs906003720 Functional Loss SNV dbSNP153 33..33 33 - - - 36920 RMVar_ID_36920 Human_SNP_ID_34303630 A-to-I Human chr1 - 153903977 153903977 153903977 CGGGCCTGGCATATCTATTTATTTTTAAGACAAGGTCTCATGCTGTTGCCAACGCTGGAGTGCAG CGGGCCTGGCATATCTATTTATTTTTAAGACAGGGTCTCATGCTGTTGCCAACGCTGGAGTGCAG T C GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1280011681 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2094743,Human_RBP_ID_10586974 36921 RMVar_ID_36921 Human_SNP_ID_34303669 A-to-I Human chr1 - 153904087 153904087 153904087 TTAGTAGAGACTGAGGTTTCTTCATGTTGGCCAGACTGGTCTCGAACTCCTGACCTCGTGATCCA TTAGTAGAGACTGAGGTTTCTTCATGTTGGCCGGACTGGTCTCGAACTCCTGACCTCGTGATCCA T C GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1321775247 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10586980 36922 RMVar_ID_36922 Human_SNP_ID_34303675 A-to-I Human chr1 - 153904117 153904117 153904117 TGCCACCACGCCCGGCTAATATTTGTATTTTTAGTAGAGACTGAGGTTTCTTCATGTTGGCCAGA TGCCACCACGCCCGGCTAATATTTGTATTTTTCGTAGAGACTGAGGTTTCTTCATGTTGGCCAGA T G GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs577256410 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10586980 36923 RMVar_ID_36923 Human_SNP_ID_34303690 A-to-I Human chr1 - 153904171 153904171 153904171 GTTTCAAATGATTTTCCTGCGTCAGCCTTCCAAGTAGCTGGGATTACAGATGCCTGCCACCACGC GTTTCAAATGATTTTCCTGCGTCAGCCTTCCAGGTAGCTGGGATTACAGATGCCTGCCACCACGC T C GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1227103456 Functional Loss SNV dbSNP153 33..33 33 - - - 36924 RMVar_ID_36924 Human_SNP_ID_34303830 A-to-I Human chr1 - 153904682 153904682 153904682 AAAAAATTAGCTGGGCCTGGTGGCACACGCCTATAGTCCCAGCTTCTTGGGAAACTGAAACAGGA AAAAAATTAGCTGGGCCTGGTGGCACACGCCTGTAGTCCCAGCTTCTTGGGAAACTGAAACAGGA T C GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1338068959 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1344837 36925 RMVar_ID_36925 Human_SNP_ID_34303831 A-to-I Human chr1 - 153904682 153904682 153904682 AAAAAATTAGCTGGGCCTGGTGGCACACGCCTATAGTCCCAGCTTCTTGGGAAACTGAAACAGGA AAAAAATTAGCTGGGCCTGGTGGCACACGCCTCTAGTCCCAGCTTCTTGGGAAACTGAAACAGGA T G GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1338068959 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1344837 36926 RMVar_ID_36926 Human_SNP_ID_34303889 A-to-I Human chr1 - 153904845 153904845 153904845 AAAATTAGCCAGATGTGGTGGCAGGCGCCTGTAATCCCACCTGCTCGGGAGGCTGAGGCAGGAGA AAAATTAGCCAGATGTGGTGGCAGGCGCCTGTGATCCCACCTGCTCGGGAGGCTGAGGCAGGAGA T C GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1413453805 Functional Loss SNV dbSNP153 33..33 33 - - - 36927 RMVar_ID_36927 Human_SNP_ID_34304013 A-to-I Human chr1 - 153905294 153905294 153905294 CTGCTCACTGCAACCTCCACCTCCCGGGTCCAAGAGATTCTCCCTGTCTCAGCCTCCCAAGTAGC CTGCTCACTGCAACCTCCACCTCCCGGGTCCAGGAGATTCTCCCTGTCTCAGCCTCCCAAGTAGC T C GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1021163136 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10587016 36928 RMVar_ID_36928 Human_SNP_ID_34304891 A-to-I Human chr1 - 153908633 153908633 153908633 AGAATCCCTGTTTCTACTAAAAGCATAAAATTAGCTGGGCGTGGTGGCACATGCTTCTAATCCCA AGAATCCCTGTTTCTACTAAAAGCATAAAATTGGCTGGGCGTGGTGGCACATGCTTCTAATCCCA T C GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs555526496 Functional Loss SNV dbSNP153 33..33 33 - - - 36929 RMVar_ID_36929 Human_SNP_ID_34305007 A-to-I Human chr1 - 153908857 153908857 153908857 AGGAGTTAGAGGCTGCAGTGACCTAGGATTGCACCACTGTGTTCCAGCCTTGGGGATAAAACACA AGGAGTTAGAGGCTGCAGTGACCTAGGATTGCCCCACTGTGTTCCAGCCTTGGGGATAAAACACA T G GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1464278627 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5692126 36930 RMVar_ID_36930 Human_SNP_ID_34305023 A-to-I Human chr1 - 153908971 153908971 153908971 GTCTCGAACTCTTGGGCTCAAGCAGTCCTCCTACCTCGGCCTCCTAAAGTGCTGAGATGTAATCC GTCTCGAACTCTTGGGCTCAAGCAGTCCTCCTGCCTCGGCCTCCTAAAGTGCTGAGATGTAATCC T C GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1319125046 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23144500 36931 RMVar_ID_36931 Human_SNP_ID_34305027 A-to-I Human chr1 - 153908980 153908980 153908980 TCCAGGCAGGTCTCGAACTCTTGGGCTCAAGCAGTCCTCCTACCTCGGCCTCCTAAAGTGCTGAG TCCAGGCAGGTCTCGAACTCTTGGGCTCAAGCGGTCCTCCTACCTCGGCCTCCTAAAGTGCTGAG T C GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs891910267 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23144500 36932 RMVar_ID_36932 Human_SNP_ID_34305134 A-to-I Human chr1 - 153909352 153909352 153909352 AAAAATTAGTCGTCATGGTGGTGGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAAATTAGTCGTCATGGTGGTGGGCGCCTGTCGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA T G GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1016592921 Functional Loss SNV dbSNP153 33..33 33 - - - 36933 RMVar_ID_36933 Human_SNP_ID_34305193 A-to-I Human chr1 - 153909557 153909557 153909557 TGACTTGTGATCTGCCTGCCGTGGCTTCCCAAAGTGCTGTGATTACAGGCATGAGCCATCGTGCC TGACTTGTGATCTGCCTGCCGTGGCTTCCCAATGTGCTGTGATTACAGGCATGAGCCATCGTGCC T A GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417257238 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557327 36934 RMVar_ID_36934 Human_SNP_ID_34306928 A-to-I Human chr1 - 153916032 153916032 153916032 CAAGTGATCCGCCCACCTGGGCCTCCCAAAGTACTGGGATTACAGGCGTGAGCCACCGCACCCGG CAAGTGATCCGCCCACCTGGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCACCCGG T C GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025426478 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24752290 36935 RMVar_ID_36935 Human_SNP_ID_34306929 A-to-I Human chr1 - 153916032 153916032 153916032 CAAGTGATCCGCCCACCTGGGCCTCCCAAAGTACTGGGATTACAGGCGTGAGCCACCGCACCCGG CAAGTGATCCGCCCACCTGGGCCTCCCAAAGTCCTGGGATTACAGGCGTGAGCCACCGCACCCGG T G GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025426478 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24752290 36936 RMVar_ID_36936 Human_SNP_ID_34306944 A-to-I Human chr1 - 153916146 153916146 153916146 CTCCTGAGTAGCTGGGATTACAGGTGTCTGCCACTACACCCAGATAATTTTTGTATTTTTAGTGG CTCCTGAGTAGCTGGGATTACAGGTGTCTGCCGCTACACCCAGATAATTTTTGTATTTTTAGTGG T C GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs528683104 Functional Loss SNV dbSNP153 33..33 33 - - - 36937 RMVar_ID_36937 Human_SNP_ID_34316454 A-to-I Human chr1 - 153949968 153949968 153949968 TATGATTGCACCACTGTACTCCAGCCTGGGCAACAGAGTGAGGCCCTGTCTCAAAAAAAGAGAAT TATGATTGCACCACTGTACTCCAGCCTGGGCAGCAGAGTGAGGCCCTGTCTCAAAAAAAGAGAAT T C CRTC2 Ensembl:ENSG00000160741 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs567174690 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_30288 36938 RMVar_ID_36938 Human_SNP_ID_34316499 A-to-I Human chr1 - 153950194 153950194 153950194 TGGTTTACTTCTAAGGCTAGGCACAGTGGCTTATGCCTGTAATCCCAGCACTTTGGGAGGCCAAG TGGTTTACTTCTAAGGCTAGGCACAGTGGCTTGTGCCTGTAATCCCAGCACTTTGGGAGGCCAAG T C CRTC2 Ensembl:ENSG00000160741 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1334746004 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_30288 36939 RMVar_ID_36939 Human_SNP_ID_34316502 A-to-I Human chr1 - 153950208 153950208 153950208 TCAAGATTTAAGAATGGTTTACTTCTAAGGCTAGGCACAGTGGCTTATGCCTGTAATCCCAGCAC TCAAGATTTAAGAATGGTTTACTTCTAAGGCTTGGCACAGTGGCTTATGCCTGTAATCCCAGCAC T A CRTC2 Ensembl:ENSG00000160741 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1170426440 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_30288 36940 RMVar_ID_36940 Human_SNP_ID_34316503 A-to-I Human chr1 - 153950208 153950208 153950208 TCAAGATTTAAGAATGGTTTACTTCTAAGGCTAGGCACAGTGGCTTATGCCTGTAATCCCAGCAC TCAAGATTTAAGAATGGTTTACTTCTAAGGCTGGGCACAGTGGCTTATGCCTGTAATCCCAGCAC T C CRTC2 Ensembl:ENSG00000160741 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1170426440 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_30288 36941 RMVar_ID_36941 Human_SNP_ID_34322147 A-to-I Human chr1 + 153970769 153970720 153970770 ATCTTTTTTTTTTTTTTTTTTTTTTTTTAGACAGAGTCTCGCTCTGTCACCAGACTGGAGTGCAG __________________________________AGTCTCGCTCTGTCACCAGACTGGAGTGCAG AAGCTAAGCATCTTAGAATCTTTTTTTTTTTTTTTTTTTTTTTTTAGACAG A CREB3L4 Ensembl:ENSG00000143578 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1431070273 Functional Loss DEL dbSNP153 1..34 33 - - - RMVar_hsa_circ_40017 36942 RMVar_ID_36942 Human_SNP_ID_34322180 A-to-I Human chr1 + 153970769 153970769 153970769 ATCTTTTTTTTTTTTTTTTTTTTTTTTTAGACAGAGTCTCGCTCTGTCACCAGACTGGAGTGCAG ATCTTTTTTTTTTTTTTTTTTTTTTTTTAGACGGAGTCTCGCTCTGTCACCAGACTGGAGTGCAG A G CREB3L4 Ensembl:ENSG00000143578 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs558109866 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40017 36943 RMVar_ID_36943 Human_SNP_ID_34325129 A-to-I Human chr1 + 153980751 153980751 153980751 CTCGAGCCCAGGCGTTCAAGACCAGCCTGGCCAACATGACAAAACCCTGTCTCCACTAAAAACAC CTCGAGCCCAGGCGTTCAAGACCAGCCTGGCCGACATGACAAAACCCTGTCTCCACTAAAAACAC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1051724589 Functional Loss SNV dbSNP153 33..33 33 - - - 36944 RMVar_ID_36944 Human_SNP_ID_34329819 A-to-I Human chr1 + 153995606 153995606 153995606 TTAAAATGCTGGTTACCACTTCTTCCTCTTCCAGGGACGTTGTCTGCAGGCACTCAGAATGGTCC TTAAAATGCTGGTTACCACTTCTTCCTCTTCCGGGGACGTTGTCTGCAGGCACTCAGAATGGTCC A G lnc-RPS27-2 RNACentral:URS00008BA34E lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1204518937 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_327213,Human_RBP_ID_3995700,Human_RBP_ID_8956308,Human_RBP_ID_10588257,Human_RBP_ID_26368836,Human_RBP_ID_26842335 36945 RMVar_ID_36945 Human_SNP_ID_34334242 A-to-I Human chr1 + 154012859 154012859 154012859 AACCCCGCCTCTACTAAAAAAAACACAAAATTAGCCGGGCTTGGTGGTGCATGCCTGTGATCCCA AACCCCGCCTCTACTAAAAAAAACACAAAATTGGCCGGGCTTGGTGGTGCATGCCTGTGATCCCA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1451520823 Functional Loss SNV dbSNP153 33..33 33 - - - 36946 RMVar_ID_36946 Human_SNP_ID_34338374 A-to-I Human chr1 + 154030545 154030545 154030545 GTCTTGAACTCGTGGCCTCAAGCGATCTGCCCACCTCAGCCTCTCAAAGTGCTGGGATTACAGTT GTCTTGAACTCGTGGCCTCAAGCGATCTGCCCGCCTCAGCCTCTCAAAGTGCTGGGATTACAGTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005566466 Functional Loss SNV dbSNP153 33..33 33 - - - 36947 RMVar_ID_36947 Human_SNP_ID_34338429 A-to-I Human chr1 + 154030835 154030835 154030835 CTTCCTGTGGCCTTGACCTCCTGAGCTCAAGCAATCCTCCCACCTCAGCCTCTCAAGTAGCCGGG CTTCCTGTGGCCTTGACCTCCTGAGCTCAAGCTATCCTCCCACCTCAGCCTCTCAAGTAGCCGGG A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs993120012 Functional Loss SNV dbSNP153 33..33 33 - - - 36948 RMVar_ID_36948 Human_SNP_ID_34338500 A-to-I Human chr1 + 154031188 154031188 154031188 TCAGCTCACTGCAACCTCCGCCTCCTGGGTTCAAGCAATTCTCCCTGTCTCAGTCCCCCAAATAG TCAGCTCACTGCAACCTCCGCCTCCTGGGTTCCAGCAATTCTCCCTGTCTCAGTCCCCCAAATAG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1258173250 Functional Loss SNV dbSNP153 33..33 33 - - - 36949 RMVar_ID_36949 Human_SNP_ID_34364369 A-to-I Human chr1 - 154140510 154140510 154140510 GGTGCCTGCCACCACGCCCAGCTAATTTTTGTATTTTTAGTGGAGATGGGGTTTCGCCATATTGG GGTGCCTGCCACCACGCCCAGCTAATTTTTGTTTTTTTAGTGGAGATGGGGTTTCGCCATATTGG T A NUP210L Ensembl:ENSG00000143552 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1260797554 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56591,RMVar_hsa_circ_136354,RMVar_hsa_circ_365395,RMVar_hsa_circ_60841,RMVar_hsa_circ_66815,RMVar_hsa_circ_65674 36950 RMVar_ID_36950 Human_SNP_ID_34369629 A-to-I Human chr1 - 154162202 154162202 154162202 TGCAACCAAGCCCGGCTAATTTTTGTGTTTTTAGTAGAGACTAGGTTTCAACATGTTAGGCTGAT TGCAACCAAGCCCGGCTAATTTTTGTGTTTTTGGTAGAGACTAGGTTTCAACATGTTAGGCTGAT T C TPM3 Ensembl:ENSG00000143549 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs929762141 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10589312 36951 RMVar_ID_36951 Human_SNP_ID_34372544 A-to-I Human chr1 - 154173917 154173917 154173917 GGAGTGCAGCAGTGCGATCTTGGCTTACTGCAACCTCTGCCTCCCGGGTTCAAGTGATTATCTTG GGAGTGCAGCAGTGCGATCTTGGCTTACTGCAGCCTCTGCCTCCCGGGTTCAAGTGATTATCTTG T C TPM3 Ensembl:ENSG00000143549 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs754163351 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85814,RMVar_hsa_circ_320725,RMVar_hsa_circ_332932,RMVar_hsa_circ_136357 36952 RMVar_ID_36952 Human_SNP_ID_34373228 A-to-I Human chr1 - 154175927 154175927 154175927 TGGCTCAAGCCCAGGAAGTTGGGGCTACAGTGAGCTCTGATTGCGCCACTGCACTCCTGGGTGAC TGGCTCAAGCCCAGGAAGTTGGGGCTACAGTGGGCTCTGATTGCGCCACTGCACTCCTGGGTGAC T C TPM3 Ensembl:ENSG00000143549 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1304057772 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85814,RMVar_hsa_circ_320725,RMVar_hsa_circ_332932,RMVar_hsa_circ_136357 36953 RMVar_ID_36953 Human_SNP_ID_34373230 A-to-I Human chr1 - 154175933 154175933 154175933 GGAGGGTGGCTCAAGCCCAGGAAGTTGGGGCTACAGTGAGCTCTGATTGCGCCACTGCACTCCTG GGAGGGTGGCTCAAGCCCAGGAAGTTGGGGCTGCAGTGAGCTCTGATTGCGCCACTGCACTCCTG T C TPM3 Ensembl:ENSG00000143549 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1249939971 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85814,RMVar_hsa_circ_320725,RMVar_hsa_circ_332932,RMVar_hsa_circ_136357 36954 RMVar_ID_36954 Human_SNP_ID_34381235 A-to-I Human chr1 - 154208184 154208184 154208184 TCCCAGACTGGTCTCAAACTCCCCTGGGCTCAAGCGATCTCTGGCCTCTGCCTCCTGAAGTGCTG TCCCAGACTGGTCTCAAACTCCCCTGGGCTCAGGCGATCTCTGGCCTCTGCCTCCTGAAGTGCTG T C C1orf43 Ensembl:ENSG00000143612 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913824413 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136359,RMVar_hsa_circ_121933 36955 RMVar_ID_36955 Human_SNP_ID_34381240 A-to-I Human chr1 - 154208212 154208212 154208212 TTTTGCAGAGATAGGGTCTCACTTTGTTTCCCAGACTGGTCTCAAACTCCCCTGGGCTCAAGCGA TTTTGCAGAGATAGGGTCTCACTTTGTTTCCCGGACTGGTCTCAAACTCCCCTGGGCTCAAGCGA T C C1orf43 Ensembl:ENSG00000143612 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1029122805 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136359,RMVar_hsa_circ_121933 36956 RMVar_ID_36956 Human_SNP_ID_34381249 A-to-I Human chr1 - 154208232 154208232 154208232 GCCACCATACCTGGCTAATTTTTTGCAGAGATAGGGTCTCACTTTGTTTCCCAGACTGGTCTCAA GCCACCATACCTGGCTAATTTTTTGCAGAGATGGGGTCTCACTTTGTTTCCCAGACTGGTCTCAA T C C1orf43 Ensembl:ENSG00000143612 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1233305905 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136359,RMVar_hsa_circ_121933 36957 RMVar_ID_36957 Human_SNP_ID_34381256 A-to-I Human chr1 - 154208274 154208274 154208274 CTCCTGCCTCAGCCTCCTGAGGAACCAGGACTACAGGTGCTTGCCACCATACCTGGCTAATTTTT CTCCTGCCTCAGCCTCCTGAGGAACCAGGACTGCAGGTGCTTGCCACCATACCTGGCTAATTTTT T C C1orf43 Ensembl:ENSG00000143612 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs777110336 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136359,RMVar_hsa_circ_121933 36958 RMVar_ID_36958 Human_SNP_ID_34381273 A-to-I Human chr1 - 154208313 154208313 154208313 ATGGCTCACTGCAGCCTCGAATTCTGGGTTCAAGCGATCCTCCTGCCTCAGCCTCCTGAGGAACC ATGGCTCACTGCAGCCTCGAATTCTGGGTTCAGGCGATCCTCCTGCCTCAGCCTCCTGAGGAACC T C C1orf43 Ensembl:ENSG00000143612 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1186997721 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136359,RMVar_hsa_circ_121933 36959 RMVar_ID_36959 Human_SNP_ID_34381284 A-to-I Human chr1 - 154208381 154208381 154208381 AGGGTGTGTGTGAGAGAGAGAGACAGGGTCTCAGTCTGTCGCCCAGACTGGAGTGCAGTGGCACA AGGGTGTGTGTGAGAGAGAGAGACAGGGTCTCTGTCTGTCGCCCAGACTGGAGTGCAGTGGCACA T A C1orf43 Ensembl:ENSG00000143612 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs571017652 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24590634 RMVar_hsa_circ_136359,RMVar_hsa_circ_121933 36960 RMVar_ID_36960 Human_SNP_ID_34381288 A-to-I Human chr1 - 154208389 154208389 154208389 ACTTTTTTAGGGTGTGTGTGAGAGAGAGAGACAGGGTCTCAGTCTGTCGCCCAGACTGGAGTGCA ACTTTTTTAGGGTGTGTGTGAGAGAGAGAGACGGGGTCTCAGTCTGTCGCCCAGACTGGAGTGCA T C C1orf43 Ensembl:ENSG00000143612 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904619899 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136359,RMVar_hsa_circ_121933 36961 RMVar_ID_36961 Human_SNP_ID_34382079 A-to-I Human chr1 - 154211276 154211276 154211276 ATTTTTGGCCGGGCGCGGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCCGAGGAGGGTGG ATTTTTGGCCGGGCGCGGTGGCTCACGCCTATGATCCCAGCACTTTGGGAGGCCGAGGAGGGTGG T C C1orf43 Ensembl:ENSG00000143612 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs976006245 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136359,RMVar_hsa_circ_121933 36962 RMVar_ID_36962 Human_SNP_ID_34382080 A-to-I Human chr1 - 154211276 154211276 154211276 ATTTTTGGCCGGGCGCGGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCCGAGGAGGGTGG ATTTTTGGCCGGGCGCGGTGGCTCACGCCTATCATCCCAGCACTTTGGGAGGCCGAGGAGGGTGG T G C1orf43 Ensembl:ENSG00000143612 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs976006245 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136359,RMVar_hsa_circ_121933 36963 RMVar_ID_36963 Human_SNP_ID_34382081 A-to-I Human chr1 - 154211278 154211278 154211278 CTATTTTTGGCCGGGCGCGGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCCGAGGAGGGT CTATTTTTGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGAGGGT T C C1orf43 Ensembl:ENSG00000143612 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1306303006 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24590670 RMVar_hsa_circ_136359,RMVar_hsa_circ_121933 36964 RMVar_ID_36964 Human_SNP_ID_34382688 A-to-I Human chr1 - 154212897 154212897 154212897 AGGGCGAGGCAGACAGATCACAGGAGGCCAGGAGTTCAAGACCAACCTAGCCAACAAGGTGAAAC AGGGCGAGGCAGACAGATCACAGGAGGCCAGGGGTTCAAGACCAACCTAGCCAACAAGGTGAAAC T C C1orf43 Ensembl:ENSG00000143612 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1433321877 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136362,RMVar_hsa_circ_136359,RMVar_hsa_circ_121933,RMVar_hsa_circ_270644,RMVar_hsa_circ_314962,RMVar_hsa_circ_136363,RMVar_hsa_circ_87644,RMVar_hsa_circ_136364,RMVar_hsa_circ_60729 36965 RMVar_ID_36965 Human_SNP_ID_34383297 A-to-I Human chr1 - 154215033 154215033 154215033 TGAGACCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAGAATAGAAAAATTAGCCAGACA TGAGACCAGCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAGAATAGAAAAATTAGCCAGACA T C C1orf43 Ensembl:ENSG00000143612 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1019099302 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8286030 RMVar_hsa_circ_136359,RMVar_hsa_circ_121933 36966 RMVar_ID_36966 Human_SNP_ID_34383318 A-to-I Human chr1 - 154215124 154215124 154215124 TGAGGCAAGAGAGGCTGGGCGCAGTAGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGC TGAGGCAAGAGAGGCTGGGCGCAGTAGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGC T C C1orf43 Ensembl:ENSG00000143612 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs897965066 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136359,RMVar_hsa_circ_121933 36967 RMVar_ID_36967 Human_SNP_ID_34383319 A-to-I Human chr1 - 154215124 154215124 154215124 TGAGGCAAGAGAGGCTGGGCGCAGTAGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGC TGAGGCAAGAGAGGCTGGGCGCAGTAGCTCACCCCTGTAATCCCAGCACTTTGGGAGGCCAAGGC T G C1orf43 Ensembl:ENSG00000143612 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs897965066 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136359,RMVar_hsa_circ_121933 36968 RMVar_ID_36968 Human_SNP_ID_34383414 A-to-I Human chr1 - 154215428 154215428 154215428 CCGAGTAGCTGGGACTACAGGACCCCGCCACAACGCCCGGCTAATTTTTTGTATTTTTAGTAGAG CCGAGTAGCTGGGACTACAGGACCCCGCCACAGCGCCCGGCTAATTTTTTGTATTTTTAGTAGAG T C C1orf43 Ensembl:ENSG00000143612 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1283861091 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136359,RMVar_hsa_circ_121933 36969 RMVar_ID_36969 Human_SNP_ID_34386886 A-to-I Human chr1 + 154227348 154227348 154227348 TTTCGGACCATAATGATGCTGACTTTGAGGAGAAGGTGAAACAAGTGAGTGTATCACTAATTTAC TTTCGGACCATAATGATGCTGACTTTGAGGAGGAGGTGAAACAAGTGAGTGTATCACTAATTTAC A G UBAP2L Ensembl:ENSG00000143569 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1368936617 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_327340,Human_RBP_ID_1412404,Human_RBP_ID_1726088,Human_RBP_ID_5693037,Human_RBP_ID_10590555,Human_RBP_ID_18966006,Human_RBP_ID_23334134,Human_RBP_ID_27798564 Human_Splice_Rec_133880,Human_Splice_Rec_133881,Human_Splice_Rec_133926,Human_Splice_Rec_133927,Human_Splice_Rec_133972,Human_Splice_Rec_133973,Human_Splice_Rec_134022,Human_Splice_Rec_134023,Human_Splice_Rec_134032,Human_Splice_Rec_134033,Human_Splice_Rec_134050,Human_Splice_Rec_134051,Human_Splice_Rec_134068,Human_Splice_Rec_134069,Human_Splice_Rec_134118,Human_Splice_Rec_134119,Human_Splice_Rec_134136,Human_Splice_Rec_134137,Human_Splice_Rec_134148,Human_Splice_Rec_134149 RMVar_hsa_circ_106772,RMVar_hsa_circ_282860,RMVar_hsa_circ_115896,RMVar_hsa_circ_121210,RMVar_hsa_circ_136366,RMVar_hsa_circ_333997,RMVar_hsa_circ_350611,RMVar_hsa_circ_359817,RMVar_hsa_circ_136367,RMVar_hsa_circ_356443,RMVar_hsa_circ_340127,RMVar_hsa_circ_317384,RMVar_hsa_circ_333460,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_136372,RMVar_hsa_circ_136369,RMVar_hsa_circ_268210,RMVar_hsa_circ_301215,RMVar_hsa_circ_335129,RMVar_hsa_circ_287167,RMVar_hsa_circ_123093,RMVar_hsa_circ_136374,RMVar_hsa_circ_60689,RMVar_hsa_circ_136375,RMVar_hsa_circ_136373 36970 RMVar_ID_36970 Human_SNP_ID_34387859 A-to-I Human chr1 + 154231413 154231413 154231413 GCCTCTGCCTCCTGGGCTCAAGCGTTTTTCCCACCTCAGCCTCCCAAGCAGCTAGGGCCACAGGT GCCTCTGCCTCCTGGGCTCAAGCGTTTTTCCCGCCTCAGCCTCCCAAGCAGCTAGGGCCACAGGT A G UBAP2L Ensembl:ENSG00000143569 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1314027684 Functional Loss SNV dbSNP153 33..33 33 - - - 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_136374,RMVar_hsa_circ_60689,RMVar_hsa_circ_136375 36971 RMVar_ID_36971 Human_SNP_ID_34388338 A-to-I Human chr1 + 154233428 154233428 154233428 GTCATTGCAACCTCCACCTCCCAGGTTCAAGCAGTTCTCCTGCTTCAGCCTCCTGAGTAGCTGGG GTCATTGCAACCTCCACCTCCCAGGTTCAAGCGGTTCTCCTGCTTCAGCCTCCTGAGTAGCTGGG A G UBAP2L Ensembl:ENSG00000143569 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1558134341 Functional Loss SNV dbSNP153 33..33 33 - - - 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_136374,RMVar_hsa_circ_60689,RMVar_hsa_circ_136375 36972 RMVar_ID_36972 Human_SNP_ID_34390881 A-to-I Human chr1 + 154243492 154243492 154243492 TCTTTTTTTTTTTGTTTTTGAGACAGAGTCTCACTGTATCGGCCAGGCTGGAGTGCAGTGGCACG TCTTTTTTTTTTTGTTTTTGAGACAGAGTCTCGCTGTATCGGCCAGGCTGGAGTGCAGTGGCACG A G UBAP2L Ensembl:ENSG00000143569 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1433030130 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10591344 RMVar_hsa_circ_6037,RMVar_hsa_circ_106772,RMVar_hsa_circ_121210,RMVar_hsa_circ_136366,RMVar_hsa_circ_333997,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_136369,RMVar_hsa_circ_268210,RMVar_hsa_circ_335129,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_290058,RMVar_hsa_circ_46680,RMVar_hsa_circ_304820,RMVar_hsa_circ_136378,RMVar_hsa_circ_9065,RMVar_hsa_circ_136377,RMVar_hsa_circ_360132,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_366844,RMVar_hsa_circ_136380,RMVar_hsa_circ_136381,RMVar_hsa_circ_313505,RMVar_hsa_circ_277382,RMVar_hsa_circ_23121,RMVar_hsa_circ_32479,RMVar_hsa_circ_121984,RMVar_hsa_circ_136382,RMVar_hsa_circ_136383,RMVar_hsa_circ_291356,RMVar_hsa_circ_85521,RMVar_hsa_circ_136385,RMVar_hsa_circ_136386,RMVar_hsa_circ_136384 36973 RMVar_ID_36973 Human_SNP_ID_34391452 A-to-I Human chr1 + 154245789 154245789 154245789 ACAAAAAAAAAAAATTAGCCGGGCGTGGTGGCAGGCACCTGTAGTCCCAGCTACAGGCTGAGGCA ACAAAAAAAAAAAATTAGCCGGGCGTGGTGGCCGGCACCTGTAGTCCCAGCTACAGGCTGAGGCA A C UBAP2L Ensembl:ENSG00000143569 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs989054920 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6037,RMVar_hsa_circ_106772,RMVar_hsa_circ_121210,RMVar_hsa_circ_136366,RMVar_hsa_circ_333997,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_136369,RMVar_hsa_circ_268210,RMVar_hsa_circ_335129,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_290058,RMVar_hsa_circ_46680,RMVar_hsa_circ_304820,RMVar_hsa_circ_136378,RMVar_hsa_circ_9065,RMVar_hsa_circ_136377,RMVar_hsa_circ_360132,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_366844,RMVar_hsa_circ_136380,RMVar_hsa_circ_136381,RMVar_hsa_circ_313505,RMVar_hsa_circ_277382,RMVar_hsa_circ_23121,RMVar_hsa_circ_32479,RMVar_hsa_circ_121984,RMVar_hsa_circ_136382,RMVar_hsa_circ_136383,RMVar_hsa_circ_291356,RMVar_hsa_circ_85521,RMVar_hsa_circ_136385,RMVar_hsa_circ_136386,RMVar_hsa_circ_136384 36974 RMVar_ID_36974 Human_SNP_ID_34391453 A-to-I Human chr1 + 154245789 154245789 154245789 ACAAAAAAAAAAAATTAGCCGGGCGTGGTGGCAGGCACCTGTAGTCCCAGCTACAGGCTGAGGCA ACAAAAAAAAAAAATTAGCCGGGCGTGGTGGCGGGCACCTGTAGTCCCAGCTACAGGCTGAGGCA A G UBAP2L Ensembl:ENSG00000143569 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs989054920 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6037,RMVar_hsa_circ_106772,RMVar_hsa_circ_121210,RMVar_hsa_circ_136366,RMVar_hsa_circ_333997,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_136369,RMVar_hsa_circ_268210,RMVar_hsa_circ_335129,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_290058,RMVar_hsa_circ_46680,RMVar_hsa_circ_304820,RMVar_hsa_circ_136378,RMVar_hsa_circ_9065,RMVar_hsa_circ_136377,RMVar_hsa_circ_360132,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_366844,RMVar_hsa_circ_136380,RMVar_hsa_circ_136381,RMVar_hsa_circ_313505,RMVar_hsa_circ_277382,RMVar_hsa_circ_23121,RMVar_hsa_circ_32479,RMVar_hsa_circ_121984,RMVar_hsa_circ_136382,RMVar_hsa_circ_136383,RMVar_hsa_circ_291356,RMVar_hsa_circ_85521,RMVar_hsa_circ_136385,RMVar_hsa_circ_136386,RMVar_hsa_circ_136384 36975 RMVar_ID_36975 Human_SNP_ID_34392504 A-to-I Human chr1 + 154249667 154249667 154249667 ATTTCTCATCACATTTAGAGGCTGGGCATGGTAGCTTACACCTGTAATCCTAGCACTTTGGGAGG ATTTCTCATCACATTTAGAGGCTGGGCATGGTGGCTTACACCTGTAATCCTAGCACTTTGGGAGG A G UBAP2L Ensembl:ENSG00000143569 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1009690323 Functional Loss SNV dbSNP153 33..33 33 - - - 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_123093,RMVar_hsa_circ_136374,RMVar_hsa_circ_136375,RMVar_hsa_circ_348380,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_23121,RMVar_hsa_circ_32479,RMVar_hsa_circ_121984,RMVar_hsa_circ_136382,RMVar_hsa_circ_85521,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_278469,RMVar_hsa_circ_351449,RMVar_hsa_circ_85902,RMVar_hsa_circ_136391,RMVar_hsa_circ_136392 36976 RMVar_ID_36976 Human_SNP_ID_34392748 A-to-I Human chr1 + 154250615 154250615 154250615 GCAGCTCATGCCTGTAATCCTAGCACTTCGAGAAGCCGAGGCGGACGGATCACTTGAGGTCAGGA GCAGCTCATGCCTGTAATCCTAGCACTTCGAGTAGCCGAGGCGGACGGATCACTTGAGGTCAGGA A T UBAP2L Ensembl:ENSG00000143569 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1396365582 Functional Loss SNV dbSNP153 33..33 33 - - - 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_123093,RMVar_hsa_circ_136374,RMVar_hsa_circ_136375,RMVar_hsa_circ_348380,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_23121,RMVar_hsa_circ_32479,RMVar_hsa_circ_121984,RMVar_hsa_circ_136382,RMVar_hsa_circ_85521,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_278469,RMVar_hsa_circ_351449,RMVar_hsa_circ_85902,RMVar_hsa_circ_136391,RMVar_hsa_circ_136392 36977 RMVar_ID_36977 Human_SNP_ID_34393131 A-to-I Human chr1 + 154251881 154251881 154251881 CTTAGGGGCTGGGTGTGATGGCTGACACTTATAATCCCAGCACTTTGGGTGGCCAAGGCAGGAGG CTTAGGGGCTGGGTGTGATGGCTGACACTTATCATCCCAGCACTTTGGGTGGCCAAGGCAGGAGG A C UBAP2L Ensembl:ENSG00000143569 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1302895542 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106772,RMVar_hsa_circ_350611,RMVar_hsa_circ_356443,RMVar_hsa_circ_340127,RMVar_hsa_circ_36383,RMVar_hsa_circ_50165,RMVar_hsa_circ_136368,RMVar_hsa_circ_268210,RMVar_hsa_circ_123093,RMVar_hsa_circ_136374,RMVar_hsa_circ_136375,RMVar_hsa_circ_46680,RMVar_hsa_circ_371865,RMVar_hsa_circ_59942,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_90884,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_136396,RMVar_hsa_circ_88890,RMVar_hsa_circ_136395,RMVar_hsa_circ_115225,RMVar_hsa_circ_136393,RMVar_hsa_circ_136398 36978 RMVar_ID_36978 Human_SNP_ID_34393402 A-to-I Human chr1 + 154252759 154252759 154252759 TTTTGTATTTTTAGTAGACATGGGGTTTCACCATGTTGTTCAGGCCAGTCTTGAACTCCTGAATG TTTTGTATTTTTAGTAGACATGGGGTTTCACCCTGTTGTTCAGGCCAGTCTTGAACTCCTGAATG A C UBAP2L Ensembl:ENSG00000143569 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1487128308 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10591570 RMVar_hsa_circ_106772,RMVar_hsa_circ_350611,RMVar_hsa_circ_356443,RMVar_hsa_circ_340127,RMVar_hsa_circ_36383,RMVar_hsa_circ_50165,RMVar_hsa_circ_136368,RMVar_hsa_circ_268210,RMVar_hsa_circ_123093,RMVar_hsa_circ_136374,RMVar_hsa_circ_136375,RMVar_hsa_circ_46680,RMVar_hsa_circ_371865,RMVar_hsa_circ_59942,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_90884,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_136396,RMVar_hsa_circ_88890,RMVar_hsa_circ_136395,RMVar_hsa_circ_115225,RMVar_hsa_circ_136393,RMVar_hsa_circ_136398 36979 RMVar_ID_36979 Human_SNP_ID_34399167 A-to-I Human chr1 + 154274481 154274481 154274481 GTTGGCCAGGCTGCTTTTGAGCTCCTGACCTCAGGTGATCCACCCACCTCGGCCTCCCAAAGTGC GTTGGCCAGGCTGCTTTTGAGCTCCTGACCTCCGGTGATCCACCCACCTCGGCCTCCCAAAGTGC A C HAX1 Ensembl:ENSG00000143575 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs950164551 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108442,RMVar_hsa_circ_136421 36980 RMVar_ID_36980 Human_SNP_ID_34399168 A-to-I Human chr1 + 154274481 154274481 154274481 GTTGGCCAGGCTGCTTTTGAGCTCCTGACCTCAGGTGATCCACCCACCTCGGCCTCCCAAAGTGC GTTGGCCAGGCTGCTTTTGAGCTCCTGACCTCGGGTGATCCACCCACCTCGGCCTCCCAAAGTGC A G HAX1 Ensembl:ENSG00000143575 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs950164551 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108442,RMVar_hsa_circ_136421 36981 RMVar_ID_36981 Human_SNP_ID_34415197 A-to-I Human chr1 + 154335510 154335510 154335510 GCCTAGGAGTTCGAAAACAGCCTGGACACCATAGTGAGACCCTGTCTTTACAAAAAACTGAAAAA GCCTAGGAGTTCGAAAACAGCCTGGACACCATGGTGAGACCCTGTCTTTACAAAAAACTGAAAAA A G ATP8B2 Ensembl:ENSG00000143515 Protein coding intron GSE38233;GSE107867 cultured B-cells;ASD brains,cerebellum - 24183664,30559470 RNA-Seq:(High) rs896600974 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128096,RMVar_hsa_circ_136427,RMVar_hsa_circ_57111,RMVar_hsa_circ_95903,RMVar_hsa_circ_136429 36982 RMVar_ID_36982 Human_SNP_ID_34442239 A-to-I Human chr1 + 154440853 154440853 154440853 TTTTGTATTTTTAGCAGAGACGGGGCTTTGCCATGTTGGCGAGGCTGCTCTTGAACTCCTGACCT TTTTGTATTTTTAGCAGAGACGGGGCTTTGCCGTGTTGGCGAGGCTGCTCTTGAACTCCTGACCT A G IL6R Ensembl:ENSG00000160712 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1398341927 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64143,RMVar_hsa_circ_353719,RMVar_hsa_circ_353746,RMVar_hsa_circ_268328,RMVar_hsa_circ_367614 36983 RMVar_ID_36983 Human_SNP_ID_34443761 A-to-I Human chr1 + 154447170 154447170 154447170 CAAAAAATATATAATAATTGGCCAGGCACGGTAGCTCATGCCTGTAATCCTAGCACTTTGGGAGG CAAAAAATATATAATAATTGGCCAGGCACGGTGGCTCATGCCTGTAATCCTAGCACTTTGGGAGG A G IL6R Ensembl:ENSG00000160712 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs531300055 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64143,RMVar_hsa_circ_353719,RMVar_hsa_circ_353746,RMVar_hsa_circ_268328,RMVar_hsa_circ_367614 36984 RMVar_ID_36984 Human_SNP_ID_34445200 A-to-I Human chr1 + 154451741 154451741 154451741 TATTTTTAGTAGAAACGGGGTTTCTCCATGTTAGTCAGGCTGGACTCGAACTCCCCACCTCAGGT TATTTTTAGTAGAAACGGGGTTTCTCCATGTTTGTCAGGCTGGACTCGAACTCCCCACCTCAGGT A T IL6R Ensembl:ENSG00000160712 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1222074414 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_353746,RMVar_hsa_circ_268328,RMVar_hsa_circ_136433,RMVar_hsa_circ_294068 36985 RMVar_ID_36985 Human_SNP_ID_34450849 A-to-I Human chr1 - 154475390 154475390 154475390 CTGAGGTCGGGAGTTCAGGACCAGCCTGGCCGACATGGGGAAACCCTGTCTCTACTAAAAAATAC CTGAGGTCGGGAGTTCAGGACCAGCCTGGCCGGCATGGGGAAACCCTGTCTCTACTAAAAAATAC T C SHE Ensembl:ENSG00000169291 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1364117091 Functional Loss SNV dbSNP153 33..33 33 - - - 36986 RMVar_ID_36986 Human_SNP_ID_34466080 A-to-I Human chr1 + 154535252 154535252 154535252 AGCCAAGCGTGGTGGTGCACACCTGTAATTCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCCCT AGCCAAGCGTGGTGGTGCACACCTGTAATTCCGGCTACTCGGGAGGCTGAGGCAGGAGAATCCCT A G TDRD10 Ensembl:ENSG00000163239 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs921343727 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59387 36987 RMVar_ID_36987 Human_SNP_ID_34479148 A-to-I Human chr1 - 154583548 154583548 154583548 CGCAGACCTGATCTTTATAGGGTTGACATAGAAAGCAGTAGTTGTGGGTGAAAGGGCAGGTTGTC CGCAGACCTGATCTTTATAGGGTTGACATAGACAGCAGTAGTTGTGGGTGAAAGGGCAGGTTGTC T G ADAR Ensembl:ENSG00000160710 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1367830616 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_743711,Human_RBP_ID_1726241,Human_RBP_ID_5693586,Human_RBP_ID_8735305,Human_RBP_ID_10592815,Human_RBP_ID_17212697,Human_RBP_ID_17330527,Human_RBP_ID_17446458,Human_RBP_ID_18217432,Human_RBP_ID_23334473,Human_RBP_ID_26386461,Human_RBP_ID_27579232 RMVar_hsa_circ_127324,RMVar_hsa_circ_136441 36988 RMVar_ID_36988 Human_SNP_ID_34560471 A-to-I Human chr1 - 154925015 154925015 154925015 TGGCCGAGGTGAGGAACAGACAGGGGGGGTCTAGATTCTGAGGGGGTTGGTGGATATTGGGCAAG TGGCCGAGGTGAGGAACAGACAGGGGGGGTCTGGATTCTGAGGGGGTTGGTGGATATTGGGCAAG T C PMVK Ensembl:ENSG00000163344 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1268139573 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3996639,Human_RBP_ID_8286303 Human_miRNA_ID_1553074,Human_miRNA_ID_1575529,Human_miRNA_ID_1582681,Human_miRNA_ID_1616651,Human_miRNA_ID_1681067,Human_miRNA_ID_2659859 RMVar_hsa_circ_136465,RMVar_hsa_circ_108951,RMVar_hsa_circ_119233,RMVar_hsa_circ_136466 36989 RMVar_ID_36989 Human_SNP_ID_34562601 A-to-I Human chr1 - 154933829 154933829 154933829 AGATGGTGCCACTGTACTCCAGCCTGGACGACAGAGTGAGACTCTGTCTCAAAAAAGAGAAAAAA AGATGGTGCCACTGTACTCCAGCCTGGACGACGGAGTGAGACTCTGTCTCAAAAAAGAGAAAAAA T C PMVK Ensembl:ENSG00000163344 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs991577490 Functional Loss SNV dbSNP153 33..33 33 - - - 36990 RMVar_ID_36990 Human_SNP_ID_34562848 A-to-I Human chr1 - 154934975 154934975 154934975 TCACCGCAACCTCTGTCTCCTGGGTTCAAGCGATTTTCCTGTCTCAGCCTCCCGAGTAGCTGGGA TCACCGCAACCTCTGTCTCCTGGGTTCAAGCGGTTTTCCTGTCTCAGCCTCCCGAGTAGCTGGGA T C PMVK Ensembl:ENSG00000163344 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs941905853 Functional Loss SNV dbSNP153 33..33 33 - - - 36991 RMVar_ID_36991 Human_SNP_ID_34563137 A-to-I Human chr1 - 154936039 154936039 154936039 CTCTTTGTTAGGTACTGTGTGCCATTATTAGCATCTCCATTTCACAGGTGAAGAAACTGAGGCTC CTCTTTGTTAGGTACTGTGTGCCATTATTAGCCTCTCCATTTCACAGGTGAAGAAACTGAGGCTC T G PMVK Ensembl:ENSG00000163344 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1169660498 Functional Loss SNV dbSNP153 33..33 33 - - - 36992 RMVar_ID_36992 Human_SNP_ID_34570713 A-to-I Human chr1 - 154964318 154964317 154964319 TTGCCCAAGCTGTTCTTGAACTCCCGGGCTCAAGTGATCCGCCTCCCTCGGCCTCCCAGAGTGCT TTGCCCAAGCTGTTCTTGAACTCCCGGGCTC__GTGATCCGCCTCCCTCGGCCTCCCAGAGTGCT CTT C SHC1 Ensembl:ENSG00000160691 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs767267109 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_17557328 Human_Splice_Rec_135506 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 36993 RMVar_ID_36993 Human_SNP_ID_34570725 A-to-I Human chr1 - 154964344 154964344 154964344 TTTGGTAGAGATGGGGTTTCGCCATGTTGCCCAAGCTGTTCTTGAACTCCCGGGCTCAAGTGATC TTTGGTAGAGATGGGGTTTCGCCATGTTGCCCCAGCTGTTCTTGAACTCCCGGGCTCAAGTGATC T G SHC1 Ensembl:ENSG00000160691 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1306596616 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557328 Human_Splice_Rec_135506 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 36994 RMVar_ID_36994 Human_SNP_ID_34570835 A-to-I Human chr1 - 154964761 154964761 154964761 TCACTGTTCTTCAAAACTTTCCTTGTTTAGCCAGGTGTGGTGGTTCATGCCTGTAATCCCAACAT TCACTGTTCTTCAAAACTTTCCTTGTTTAGCCTGGTGTGGTGGTTCATGCCTGTAATCCCAACAT T A SHC1 Ensembl:ENSG00000160691 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1195694544 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19196783 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 36995 RMVar_ID_36995 Human_SNP_ID_34576158 A-to-I Human chr1 + 154984538 154984538 154984538 GTTCGAGACCAGCCTCAACATGGAGAAACCCCATCTCTACTAAAAATACAAAATTAGCCAGGCGT GTTCGAGACCAGCCTCAACATGGAGAAACCCCCTCTCTACTAAAAATACAAAATTAGCCAGGCGT A C FLAD1 Ensembl:ENSG00000160688 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1210535624 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136485,RMVar_hsa_circ_127024,RMVar_hsa_circ_100202,RMVar_hsa_circ_90198,RMVar_hsa_circ_136484,RMVar_hsa_circ_329794,RMVar_hsa_circ_136486,RMVar_hsa_circ_58525 36996 RMVar_ID_36996 Human_SNP_ID_34576160 A-to-I Human chr1 + 154984550 154984550 154984550 CCTCAACATGGAGAAACCCCATCTCTACTAAAAATACAAAATTAGCCAGGCGTGGTGGTGCATGC CCTCAACATGGAGAAACCCCATCTCTACTAAACATACAAAATTAGCCAGGCGTGGTGGTGCATGC A C FLAD1 Ensembl:ENSG00000160688 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1467950401 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136485,RMVar_hsa_circ_127024,RMVar_hsa_circ_100202,RMVar_hsa_circ_90198,RMVar_hsa_circ_136484,RMVar_hsa_circ_329794,RMVar_hsa_circ_136486,RMVar_hsa_circ_58525 36997 RMVar_ID_36997 Human_SNP_ID_34576276 A-to-I Human chr1 + 154984951 154984951 154984951 CAGTGGCACAGTCACAGCTCACTGAAGCCTCCATCTTCCAGGCTCAAGCAGTCCTCCTGCCTCAG CAGTGGCACAGTCACAGCTCACTGAAGCCTCCCTCTTCCAGGCTCAAGCAGTCCTCCTGCCTCAG A C FLAD1 Ensembl:ENSG00000160688 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs901413868 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136485,RMVar_hsa_circ_127024,RMVar_hsa_circ_100202,RMVar_hsa_circ_90198,RMVar_hsa_circ_136484,RMVar_hsa_circ_329794,RMVar_hsa_circ_136486,RMVar_hsa_circ_58525 36998 RMVar_ID_36998 Human_SNP_ID_34577021 A-to-I Human chr1 + 154987226 154987226 154987226 ATTTTTGTATTTTTTTGTAGAGATGGGGTTTTACCATACTGTGCCGGTTGGTCTCGAACTTCTGA ATTTTTGTATTTTTTTGTAGAGATGGGGTTTTGCCATACTGTGCCGGTTGGTCTCGAACTTCTGA A G FLAD1 Ensembl:ENSG00000160688 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs928307815 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22128457 RMVar_hsa_circ_136485,RMVar_hsa_circ_127024,RMVar_hsa_circ_100202,RMVar_hsa_circ_90198,RMVar_hsa_circ_136484,RMVar_hsa_circ_329794,RMVar_hsa_circ_136486,RMVar_hsa_circ_58525 36999 RMVar_ID_36999 Human_SNP_ID_34577122 A-to-I Human chr1 + 154987675 154987675 154987675 AAGAAGAAAGCAGGCCAGGCGTGGTGGCTCACACCTATAATTCCAGCACTTTGGGAGGCTGAGGC AAGAAGAAAGCAGGCCAGGCGTGGTGGCTCACGCCTATAATTCCAGCACTTTGGGAGGCTGAGGC A G FLAD1 Ensembl:ENSG00000160688 Protein coding exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs958083085 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136485,RMVar_hsa_circ_127024,RMVar_hsa_circ_100202,RMVar_hsa_circ_90198,RMVar_hsa_circ_136484,RMVar_hsa_circ_329794,RMVar_hsa_circ_136486,RMVar_hsa_circ_58525 37000 RMVar_ID_37000 Human_SNP_ID_34577162 A-to-I Human chr1 + 154987895 154987895 154987895 TTGAGGCTGCAGTGAACTGTGACTGAGCCACTATACTCCAGCCTGGGTGACAGAGACCCAGCTTT TTGAGGCTGCAGTGAACTGTGACTGAGCCACTGTACTCCAGCCTGGGTGACAGAGACCCAGCTTT A G FLAD1 Ensembl:ENSG00000160688 Protein coding exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs932760531 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136485,RMVar_hsa_circ_127024,RMVar_hsa_circ_100202,RMVar_hsa_circ_90198,RMVar_hsa_circ_136484,RMVar_hsa_circ_329794,RMVar_hsa_circ_136486,RMVar_hsa_circ_58525 37001 RMVar_ID_37001 Human_SNP_ID_34579762 A-to-I Human chr1 - 154996767 154996767 154996767 CTCTGTCTCAAAAAAAAAAAATCGAAATTAGCAGGACATGGTGGTACGCTCCTGTAATCCCAGCT CTCTGTCTCAAAAAAAAAAAATCGAAATTAGCGGGACATGGTGGTACGCTCCTGTAATCCCAGCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs919364572 Functional Loss SNV dbSNP153 33..33 33 - - - 37002 RMVar_ID_37002 Human_SNP_ID_34596173 A-to-I Human chr1 + 155054743 155054743 155054743 CTTACAAAAAGTATCTGGGCATGGTGGCGTGCACCCGTAGTTCCAGCCACTCAGGAGGCCGAAGT CTTACAAAAAGTATCTGGGCATGGTGGCGTGCCCCCGTAGTTCCAGCCACTCAGGAGGCCGAAGT A C ADAM15 Ensembl:ENSG00000143537 Protein coding intron GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829 esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line - 29796672,31158229 RNA-Seq:(High) rs569036944 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_332006,RMVar_hsa_circ_370093,RMVar_hsa_circ_112614,RMVar_hsa_circ_136495,RMVar_hsa_circ_136496,RMVar_hsa_circ_136497,RMVar_hsa_circ_77553,RMVar_hsa_circ_136498,RMVar_hsa_circ_76914,RMVar_hsa_circ_136499 37003 RMVar_ID_37003 Human_SNP_ID_34616444 A-to-I Human chr1 + 155133108 155133108 155133108 AATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATATTGGCCAGGCTGGTCTCGAACTCCTGA AATTTTTGTATTTTTAGTAGAGACGGGGTTTCCCCATATTGGCCAGGCTGGTCTCGAACTCCTGA A C EFNA1 Ensembl:ENSG00000169242 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1156337344 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59688 37004 RMVar_ID_37004 Human_SNP_ID_34626369 A-to-I Human chr1 - 155170901 155170901 155170901 GGGAAGCTGAGGTGGGATGATCGCTTGAGCCCAGGAGATCAAGGCTGCAGTGAGCTGAAACTGCA GGGAAGCTGAGGTGGGATGATCGCTTGAGCCCTGGAGATCAAGGCTGCAGTGAGCTGAAACTGCA T A KRTCAP2,AL713999.1 Ensembl:ENSG00000163463,Ensembl:ENSG00000273088 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1188420086 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95930,RMVar_hsa_circ_106385,RMVar_hsa_circ_136508,RMVar_hsa_circ_136509 37005 RMVar_ID_37005 Human_SNP_ID_34626422 A-to-I Human chr1 - 155171082 155171082 155171082 CCATTGGCTGGGTGGGATGGCACACGCCTGTAATCCTAGCACTTTGGGAGGTGTAGGCTGGCAGA CCATTGGCTGGGTGGGATGGCACACGCCTGTATTCCTAGCACTTTGGGAGGTGTAGGCTGGCAGA T A KRTCAP2,AL713999.1 Ensembl:ENSG00000163463,Ensembl:ENSG00000273088 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569553776 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95930,RMVar_hsa_circ_106385,RMVar_hsa_circ_136508,RMVar_hsa_circ_136509 37006 RMVar_ID_37006 Human_SNP_ID_34626455 A-to-I Human chr1 - 155171236 155171236 155171236 TTTTGTATTTTTGGTAGAGATAGGATTTCACCATGTTGGTTAGGCTGGTCTTGAACTCCTGACCT TTTTGTATTTTTGGTAGAGATAGGATTTCACCGTGTTGGTTAGGCTGGTCTTGAACTCCTGACCT T C KRTCAP2,AL713999.1 Ensembl:ENSG00000163463,Ensembl:ENSG00000273088 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs972568927 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95930,RMVar_hsa_circ_106385,RMVar_hsa_circ_136508,RMVar_hsa_circ_136509 37007 RMVar_ID_37007 Human_SNP_ID_34629957 A-to-I Human chr1 + 155183186 155183186 155183186 CCCACCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGTGCCTGGCCCCAACTCCC CCCACCTTGGCCTCCCAAAGTGCTGGGATTACGGGCGTGAGCCACTGTGCCTGGCCCCAACTCCC A G TRIM46 Ensembl:ENSG00000163462 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs570718617 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93787,RMVar_hsa_circ_136514 37008 RMVar_ID_37008 Human_SNP_ID_34635593 A-to-I Human chr1 - 155203976 155203976 155203976 AAAATTAGCTGGGCATGGTGGTGGGCACCTGTAGTCCCAGCTACTTGGGAGGCGGAGGCAGGAGA AAAATTAGCTGGGCATGGTGGTGGGCACCTGTCGTCCCAGCTACTTGGGAGGCGGAGGCAGGAGA T G THBS3 Ensembl:ENSG00000169231 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs977589169 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17320,RMVar_hsa_circ_49762,RMVar_hsa_circ_107213,RMVar_hsa_circ_136519 37009 RMVar_ID_37009 Human_SNP_ID_34635694 A-to-I Human chr1 - 155204481 155204481 155204481 AGTTCAAGTGATTCTCCTGCCTCAGCCTCCCAAGCAGCTGGGATTACAGGCGCCCTCCACCATGC AGTTCAAGTGATTCTCCTGCCTCAGCCTCCCAGGCAGCTGGGATTACAGGCGCCCTCCACCATGC T C THBS3 Ensembl:ENSG00000169231 Protein coding intron GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs939677939 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17320,RMVar_hsa_circ_49762,RMVar_hsa_circ_107213,RMVar_hsa_circ_136519 37010 RMVar_ID_37010 Human_SNP_ID_34640639 A-to-I Human chr1 - 155221461 155221461 155221461 CCTCAGCCTCCCAAAGTGCTGGGATTATAGGCATGAGCTACCGTGCCCAGCCACCCTGGAAAAAT CCTCAGCCTCCCAAAGTGCTGGGATTATAGGCGTGAGCTACCGTGCCCAGCCACCCTGGAAAAAT T C GBAP1 Ensembl:ENSG00000160766 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs889792410 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136524,RMVar_hsa_circ_136525,RMVar_hsa_circ_83923,RMVar_hsa_circ_136526,RMVar_hsa_circ_136528 37011 RMVar_ID_37011 Human_SNP_ID_34640646 A-to-I Human chr1 - 155221506 155221506 155221506 TTTTGCCATGTTGGCCATGAACACCTGTCCTCAAGCTATCCACTGCCTCAGCCTCCCAAAGTGCT TTTTGCCATGTTGGCCATGAACACCTGTCCTCCAGCTATCCACTGCCTCAGCCTCCCAAAGTGCT T G GBAP1 Ensembl:ENSG00000160766 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1354249236 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17558529 RMVar_hsa_circ_136524,RMVar_hsa_circ_136525,RMVar_hsa_circ_83923,RMVar_hsa_circ_136526,RMVar_hsa_circ_136528 37012 RMVar_ID_37012 Human_SNP_ID_34640655 A-to-I Human chr1 - 155221570 155221570 155221570 AGCTGGGATTACAGGCGTGCACCACCACACCCAGCTAATTTTTGTATTTTCATTTCAGATGGGAT AGCTGGGATTACAGGCGTGCACCACCACACCCTGCTAATTTTTGTATTTTCATTTCAGATGGGAT T A GBAP1 Ensembl:ENSG00000160766 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1047207899 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136524,RMVar_hsa_circ_136525,RMVar_hsa_circ_83923,RMVar_hsa_circ_136526,RMVar_hsa_circ_136528 37013 RMVar_ID_37013 Human_SNP_ID_34640656 A-to-I Human chr1 - 155221570 155221570 155221570 AGCTGGGATTACAGGCGTGCACCACCACACCCAGCTAATTTTTGTATTTTCATTTCAGATGGGAT AGCTGGGATTACAGGCGTGCACCACCACACCCGGCTAATTTTTGTATTTTCATTTCAGATGGGAT T C GBAP1 Ensembl:ENSG00000160766 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1047207899 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136524,RMVar_hsa_circ_136525,RMVar_hsa_circ_83923,RMVar_hsa_circ_136526,RMVar_hsa_circ_136528 37014 RMVar_ID_37014 Human_SNP_ID_34640680 A-to-I Human chr1 - 155221651 155221651 155221651 GGAGTGCAGTGGCACAATCTTGGGTCTCTGCAACCTCTGACTCCTGGGTTCAAGTGATTCTCGTA GGAGTGCAGTGGCACAATCTTGGGTCTCTGCAGCCTCTGACTCCTGGGTTCAAGTGATTCTCGTA T C GBAP1 Ensembl:ENSG00000160766 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs970702313 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136524,RMVar_hsa_circ_136525,RMVar_hsa_circ_83923,RMVar_hsa_circ_136526,RMVar_hsa_circ_136528 37015 RMVar_ID_37015 Human_SNP_ID_34640697 A-to-I Human chr1 - 155221708 155221707 155221709 TATCCACCTTGGAAATTTTTTTTTTTTGAAACAGAGTGTTACTCTGTCTCCCAGGCTGGAGTGCA TATCCACCTTGGAAATTTTTTTTTTTTGAAA__GAGTGTTACTCTGTCTCCCAGGCTGGAGTGCA CTG C GBAP1 Ensembl:ENSG00000160766 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1331268964 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_136524,RMVar_hsa_circ_136525,RMVar_hsa_circ_83923,RMVar_hsa_circ_136526,RMVar_hsa_circ_136528 37016 RMVar_ID_37016 Human_SNP_ID_34640698 A-to-I Human chr1 - 155221708 155221708 155221708 TATCCACCTTGGAAATTTTTTTTTTTTGAAACAGAGTGTTACTCTGTCTCCCAGGCTGGAGTGCA TATCCACCTTGGAAATTTTTTTTTTTTGAAACGGAGTGTTACTCTGTCTCCCAGGCTGGAGTGCA T C GBAP1 Ensembl:ENSG00000160766 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1211554736 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136524,RMVar_hsa_circ_136525,RMVar_hsa_circ_83923,RMVar_hsa_circ_136526,RMVar_hsa_circ_136528 37017 RMVar_ID_37017 Human_SNP_ID_34640846 A-to-I Human chr1 - 155222170 155222170 155222170 CAACATGGTAAAACCCCGTCTTGACTAAAAATACAAAAATCAGCCAGGCATGGTGGTGTGCGTCT CAACATGGTAAAACCCCGTCTTGACTAAAAATGCAAAAATCAGCCAGGCATGGTGGTGTGCGTCT T C GBAP1 Ensembl:ENSG00000160766 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1389114630 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136524,RMVar_hsa_circ_136525,RMVar_hsa_circ_83923,RMVar_hsa_circ_136526,RMVar_hsa_circ_136528 37018 RMVar_ID_37018 Human_SNP_ID_34640847 A-to-I Human chr1 - 155222170 155222170 155222170 CAACATGGTAAAACCCCGTCTTGACTAAAAATACAAAAATCAGCCAGGCATGGTGGTGTGCGTCT CAACATGGTAAAACCCCGTCTTGACTAAAAATCCAAAAATCAGCCAGGCATGGTGGTGTGCGTCT T G GBAP1 Ensembl:ENSG00000160766 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1389114630 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136524,RMVar_hsa_circ_136525,RMVar_hsa_circ_83923,RMVar_hsa_circ_136526,RMVar_hsa_circ_136528 37019 RMVar_ID_37019 Human_SNP_ID_34641293 A-to-I Human chr1 - 155224072 155224072 155224072 GTGCACTTCTGGTCCCAGCTACTCAGGAGGCTAAGGTGGGAGGATCCCTTGAGCCCAGGTGGTCG GTGCACTTCTGGTCCCAGCTACTCAGGAGGCTGAGGTGGGAGGATCCCTTGAGCCCAGGTGGTCG T C GBAP1 Ensembl:ENSG00000160766 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs368950640 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136524,RMVar_hsa_circ_136525,RMVar_hsa_circ_83923,RMVar_hsa_circ_136526,RMVar_hsa_circ_136528 37020 RMVar_ID_37020 Human_SNP_ID_34641296 A-to-I Human chr1 - 155224080 155224080 155224080 GTGGTGGTGTGCACTTCTGGTCCCAGCTACTCAGGAGGCTAAGGTGGGAGGATCCCTTGAGCCCA GTGGTGGTGTGCACTTCTGGTCCCAGCTACTCCGGAGGCTAAGGTGGGAGGATCCCTTGAGCCCA T G GBAP1 Ensembl:ENSG00000160766 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1324088387 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136524,RMVar_hsa_circ_136525,RMVar_hsa_circ_83923,RMVar_hsa_circ_136526,RMVar_hsa_circ_136528 37021 RMVar_ID_37021 Human_SNP_ID_34666933 A-to-I Human chr1 + 155314019 155314019 155314019 TTTTGTATTTTTAGTAGAGACGGGGTTTCACCATATTGGTCAGGCTGGTCTGGAACTCCTGACCT TTTTGTATTTTTAGTAGAGACGGGGTTTCACCGTATTGGTCAGGCTGGTCTGGAACTCCTGACCT A G FDPS Ensembl:ENSG00000160752 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1007812796 Functional Loss SNV dbSNP153 33..33 33 - - - 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 37022 RMVar_ID_37022 Human_SNP_ID_34666937 A-to-I Human chr1 + 155314028 155314028 155314028 TTTAGTAGAGACGGGGTTTCACCATATTGGTCAGGCTGGTCTGGAACTCCTGACCTTGTGATCCA TTTAGTAGAGACGGGGTTTCACCATATTGGTCGGGCTGGTCTGGAACTCCTGACCTTGTGATCCA A G FDPS Ensembl:ENSG00000160752 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs955902142 Functional Loss SNV dbSNP153 33..33 33 - - - 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 37023 RMVar_ID_37023 Human_SNP_ID_34666988 A-to-I Human chr1 + 155314225 155314225 155314225 TTTTTTTTTTTGATACAGGGTCTTACTCTGTTACCCAGGCTGGAGTGCAGTGGCATGATCTTGGC TTTTTTTTTTTGATACAGGGTCTTACTCTGTTGCCCAGGCTGGAGTGCAGTGGCATGATCTTGGC A G FDPS Ensembl:ENSG00000160752 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs190453202 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11175411 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 37024 RMVar_ID_37024 Human_SNP_ID_34667078 A-to-I Human chr1 + 155314614 155314614 155314614 CTTCCACCTCAGCCTCCCAAGTAGCTGAGACTACAGGTGCCTACCACCACGCCCGGCTTTTTAAA CTTCCACCTCAGCCTCCCAAGTAGCTGAGACTTCAGGTGCCTACCACCACGCCCGGCTTTTTAAA A T FDPS Ensembl:ENSG00000160752 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1201911650 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22847681 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 37025 RMVar_ID_37025 Human_SNP_ID_34667226 A-to-I Human chr1 + 155315361 155315361 155315361 GAGGTCAGGAGTTCGAGACCAGCCTGACCAACATGGGGAAACCCCATCTCTACTGAAAATACAAA GAGGTCAGGAGTTCGAGACCAGCCTGACCAACGTGGGGAAACCCCATCTCTACTGAAAATACAAA A G FDPS Ensembl:ENSG00000160752 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 31158229,32596459 RNA-Seq:(High) rs956384857 Functional Loss SNV dbSNP153 33..33 33 - - - 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 37026 RMVar_ID_37026 Human_SNP_ID_34667262 A-to-I Human chr1 + 155315494 155315494 155315494 GAAGTCAGGAGATCGAGACCATCCTGGCTAACATGGTGAAACCCCGTCTCTACTAAGAATACAAA GAAGTCAGGAGATCGAGACCATCCTGGCTAACGTGGTGAAACCCCGTCTCTACTAAGAATACAAA A G FDPS Ensembl:ENSG00000160752 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs531814914 Functional Loss SNV dbSNP153 33..33 33 - - - 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 37027 RMVar_ID_37027 Human_SNP_ID_34667266 A-to-I Human chr1 + 155315501 155315501 155315501 GGAGATCGAGACCATCCTGGCTAACATGGTGAAACCCCGTCTCTACTAAGAATACAAAAAAAATA GGAGATCGAGACCATCCTGGCTAACATGGTGACACCCCGTCTCTACTAAGAATACAAAAAAAATA A C FDPS Ensembl:ENSG00000160752 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1319171056 Functional Loss SNV dbSNP153 33..33 33 - - - 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 37028 RMVar_ID_37028 Human_SNP_ID_34667278 A-to-I Human chr1 + 155315536 155315536 155315536 CCCGTCTCTACTAAGAATACAAAAAAAATATTAGCCGGGCATGGTGGCAGGCGCCTGTAGTCCCA CCCGTCTCTACTAAGAATACAAAAAAAATATTGGCCGGGCATGGTGGCAGGCGCCTGTAGTCCCA A G FDPS Ensembl:ENSG00000160752 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1030850191 Functional Loss SNV dbSNP153 33..33 33 - - - 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 37029 RMVar_ID_37029 Human_SNP_ID_34667298 A-to-I Human chr1 + 155315589 155315589 155315589 CCTGTAGTCCCAGCTATTTGGGAGGCTGAGGTAGGAGAATGGCGTGAACCTGGGAGGCGGAGCTT CCTGTAGTCCCAGCTATTTGGGAGGCTGAGGTGGGAGAATGGCGTGAACCTGGGAGGCGGAGCTT A G FDPS Ensembl:ENSG00000160752 Protein coding intron GSE38233;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;Bronchiolar epithelium,BERP35T4 cell line - 24183664,31158229 RNA-Seq:(High) rs1188051691 Functional Loss SNV dbSNP153 33..33 33 - - - 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 37030 RMVar_ID_37030 Human_SNP_ID_34679098 A-to-I Human chr1 - 155357909 155357909 155357909 AAAATTAGCCTGGCATAGTGGCACGCACCTGTAATGTCAGCTACTGGGGAGGCTGAGATAGGAGG AAAATTAGCCTGGCATAGTGGCACGCACCTGTCATGTCAGCTACTGGGGAGGCTGAGATAGGAGG T G ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1027363762 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2591,RMVar_hsa_circ_42667,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_136594,RMVar_hsa_circ_110760,RMVar_hsa_circ_97081,RMVar_hsa_circ_360900,RMVar_hsa_circ_136598,RMVar_hsa_circ_369334,RMVar_hsa_circ_11734,RMVar_hsa_circ_136602,RMVar_hsa_circ_136603,RMVar_hsa_circ_136601,RMVar_hsa_circ_123722,RMVar_hsa_circ_332494,RMVar_hsa_circ_85679,RMVar_hsa_circ_15659,RMVar_hsa_circ_42461,RMVar_hsa_circ_351218,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_118802,RMVar_hsa_circ_136607,RMVar_hsa_circ_22549,RMVar_hsa_circ_136608,RMVar_hsa_circ_102723,RMVar_hsa_circ_136610 37031 RMVar_ID_37031 Human_SNP_ID_34679248 A-to-I Human chr1 - 155358496 155358496 155358496 TTTTTTTAGTAGAGACTGGGTTTTACCATGTTAGCCAGGATGGTCTCGATCTGCTGACCTTGTGA TTTTTTTAGTAGAGACTGGGTTTTACCATGTTGGCCAGGATGGTCTCGATCTGCTGACCTTGTGA T C ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs143341259 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2591,RMVar_hsa_circ_42667,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_136594,RMVar_hsa_circ_110760,RMVar_hsa_circ_97081,RMVar_hsa_circ_360900,RMVar_hsa_circ_136598,RMVar_hsa_circ_369334,RMVar_hsa_circ_11734,RMVar_hsa_circ_136602,RMVar_hsa_circ_136603,RMVar_hsa_circ_136601,RMVar_hsa_circ_123722,RMVar_hsa_circ_332494,RMVar_hsa_circ_85679,RMVar_hsa_circ_15659,RMVar_hsa_circ_42461,RMVar_hsa_circ_351218,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_118802,RMVar_hsa_circ_136607,RMVar_hsa_circ_22549,RMVar_hsa_circ_136608,RMVar_hsa_circ_102723,RMVar_hsa_circ_136610 37032 RMVar_ID_37032 Human_SNP_ID_34679330 A-to-I Human chr1 - 155358657 155358657 155358657 TTGAGGTGGAGTCTCACTCTGTCTCCCAGGCTAGAGTGCAGTGGCGTGATCTCGGCTTGCTGCAA TTGAGGTGGAGTCTCACTCTGTCTCCCAGGCTGGAGTGCAGTGGCGTGATCTCGGCTTGCTGCAA T C ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs538725637 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2591,RMVar_hsa_circ_42667,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_136594,RMVar_hsa_circ_110760,RMVar_hsa_circ_97081,RMVar_hsa_circ_360900,RMVar_hsa_circ_136598,RMVar_hsa_circ_369334,RMVar_hsa_circ_11734,RMVar_hsa_circ_136602,RMVar_hsa_circ_136603,RMVar_hsa_circ_136601,RMVar_hsa_circ_123722,RMVar_hsa_circ_332494,RMVar_hsa_circ_85679,RMVar_hsa_circ_15659,RMVar_hsa_circ_42461,RMVar_hsa_circ_351218,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_118802,RMVar_hsa_circ_136607,RMVar_hsa_circ_22549,RMVar_hsa_circ_136608,RMVar_hsa_circ_102723,RMVar_hsa_circ_136610 37033 RMVar_ID_37033 Human_SNP_ID_34679392 A-to-I Human chr1 - 155358859 155358859 155358859 CTCCCACCTCAGCCTCCCACAGTGCTGGGACTACAGACCTGAGCCACCATGCCCAGCCAAATTTT CTCCCACCTCAGCCTCCCACAGTGCTGGGACTGCAGACCTGAGCCACCATGCCCAGCCAAATTTT T C ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1436256365 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2591,RMVar_hsa_circ_42667,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_136594,RMVar_hsa_circ_110760,RMVar_hsa_circ_97081,RMVar_hsa_circ_360900,RMVar_hsa_circ_136598,RMVar_hsa_circ_369334,RMVar_hsa_circ_11734,RMVar_hsa_circ_136602,RMVar_hsa_circ_136603,RMVar_hsa_circ_136601,RMVar_hsa_circ_123722,RMVar_hsa_circ_332494,RMVar_hsa_circ_85679,RMVar_hsa_circ_15659,RMVar_hsa_circ_42461,RMVar_hsa_circ_351218,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_118802,RMVar_hsa_circ_136607,RMVar_hsa_circ_22549,RMVar_hsa_circ_136608,RMVar_hsa_circ_102723,RMVar_hsa_circ_136610 37034 RMVar_ID_37034 Human_SNP_ID_34682627 A-to-I Human chr1 - 155371799 155371799 155371799 ATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCTCTTGAACCTGGGAAGCGGAGTTTGCAGTG ATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAGTCTCTTGAACCTGGGAAGCGGAGTTTGCAGTG T C ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs935490878 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42667,RMVar_hsa_circ_368935,RMVar_hsa_circ_366827,RMVar_hsa_circ_358498,RMVar_hsa_circ_69363,RMVar_hsa_circ_55904,RMVar_hsa_circ_136579,RMVar_hsa_circ_91291,RMVar_hsa_circ_136577,RMVar_hsa_circ_370041,RMVar_hsa_circ_356619,RMVar_hsa_circ_91812,RMVar_hsa_circ_55595,RMVar_hsa_circ_136580,RMVar_hsa_circ_106304,RMVar_hsa_circ_67956,RMVar_hsa_circ_136588,RMVar_hsa_circ_107116,RMVar_hsa_circ_136592,RMVar_hsa_circ_78519,RMVar_hsa_circ_36517,RMVar_hsa_circ_71110,RMVar_hsa_circ_136595,RMVar_hsa_circ_136594,RMVar_hsa_circ_110760,RMVar_hsa_circ_97081,RMVar_hsa_circ_360900,RMVar_hsa_circ_136598,RMVar_hsa_circ_11734,RMVar_hsa_circ_136603,RMVar_hsa_circ_85679,RMVar_hsa_circ_42461,RMVar_hsa_circ_136606,RMVar_hsa_circ_55666,RMVar_hsa_circ_357101,RMVar_hsa_circ_118802,RMVar_hsa_circ_136607,RMVar_hsa_circ_22549,RMVar_hsa_circ_102723,RMVar_hsa_circ_59208,RMVar_hsa_circ_66639,RMVar_hsa_circ_136610,RMVar_hsa_circ_363166,RMVar_hsa_circ_285466,RMVar_hsa_circ_61432,RMVar_hsa_circ_332675,RMVar_hsa_circ_136612,RMVar_hsa_circ_136613,RMVar_hsa_circ_343437,RMVar_hsa_circ_318341,RMVar_hsa_circ_298012,RMVar_hsa_circ_136616,RMVar_hsa_circ_136617,RMVar_hsa_circ_136618,RMVar_hsa_circ_136615 37035 RMVar_ID_37035 Human_SNP_ID_34682870 A-to-I Human chr1 - 155372684 155372684 155372684 ATCCCTTGAGCCAAGGAGTTCGAGGCTACAGTAGGCTGTGATCAGGCCACTGCACCCCAGTCTGG ATCCCTTGAGCCAAGGAGTTCGAGGCTACAGTGGGCTGTGATCAGGCCACTGCACCCCAGTCTGG T C ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1358199910 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42667,RMVar_hsa_circ_368935,RMVar_hsa_circ_366827,RMVar_hsa_circ_358498,RMVar_hsa_circ_69363,RMVar_hsa_circ_55904,RMVar_hsa_circ_136579,RMVar_hsa_circ_91291,RMVar_hsa_circ_136577,RMVar_hsa_circ_370041,RMVar_hsa_circ_356619,RMVar_hsa_circ_91812,RMVar_hsa_circ_55595,RMVar_hsa_circ_136580,RMVar_hsa_circ_106304,RMVar_hsa_circ_67956,RMVar_hsa_circ_136588,RMVar_hsa_circ_107116,RMVar_hsa_circ_136592,RMVar_hsa_circ_78519,RMVar_hsa_circ_36517,RMVar_hsa_circ_71110,RMVar_hsa_circ_136595,RMVar_hsa_circ_136594,RMVar_hsa_circ_110760,RMVar_hsa_circ_97081,RMVar_hsa_circ_360900,RMVar_hsa_circ_136598,RMVar_hsa_circ_11734,RMVar_hsa_circ_136603,RMVar_hsa_circ_85679,RMVar_hsa_circ_42461,RMVar_hsa_circ_136606,RMVar_hsa_circ_55666,RMVar_hsa_circ_357101,RMVar_hsa_circ_118802,RMVar_hsa_circ_136607,RMVar_hsa_circ_22549,RMVar_hsa_circ_102723,RMVar_hsa_circ_59208,RMVar_hsa_circ_66639,RMVar_hsa_circ_136610,RMVar_hsa_circ_363166,RMVar_hsa_circ_285466,RMVar_hsa_circ_61432,RMVar_hsa_circ_332675,RMVar_hsa_circ_136612,RMVar_hsa_circ_136613,RMVar_hsa_circ_343437,RMVar_hsa_circ_318341,RMVar_hsa_circ_298012,RMVar_hsa_circ_136616,RMVar_hsa_circ_136617,RMVar_hsa_circ_136618,RMVar_hsa_circ_136615 37036 RMVar_ID_37036 Human_SNP_ID_34682884 A-to-I Human chr1 - 155372749 155372749 155372749 GTTAAGGCTGGGTGTGGTAGTTCATGCCTGTAATCCCACCTACTCAGGAGGCCGAGGCAGGATGG GTTAAGGCTGGGTGTGGTAGTTCATGCCTGTAGTCCCACCTACTCAGGAGGCCGAGGCAGGATGG T C ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs538289590 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42667,RMVar_hsa_circ_368935,RMVar_hsa_circ_366827,RMVar_hsa_circ_358498,RMVar_hsa_circ_69363,RMVar_hsa_circ_55904,RMVar_hsa_circ_136579,RMVar_hsa_circ_91291,RMVar_hsa_circ_136577,RMVar_hsa_circ_370041,RMVar_hsa_circ_356619,RMVar_hsa_circ_91812,RMVar_hsa_circ_55595,RMVar_hsa_circ_136580,RMVar_hsa_circ_106304,RMVar_hsa_circ_67956,RMVar_hsa_circ_136588,RMVar_hsa_circ_107116,RMVar_hsa_circ_136592,RMVar_hsa_circ_78519,RMVar_hsa_circ_36517,RMVar_hsa_circ_71110,RMVar_hsa_circ_136595,RMVar_hsa_circ_136594,RMVar_hsa_circ_110760,RMVar_hsa_circ_97081,RMVar_hsa_circ_360900,RMVar_hsa_circ_136598,RMVar_hsa_circ_11734,RMVar_hsa_circ_136603,RMVar_hsa_circ_85679,RMVar_hsa_circ_42461,RMVar_hsa_circ_136606,RMVar_hsa_circ_55666,RMVar_hsa_circ_357101,RMVar_hsa_circ_118802,RMVar_hsa_circ_136607,RMVar_hsa_circ_22549,RMVar_hsa_circ_102723,RMVar_hsa_circ_59208,RMVar_hsa_circ_66639,RMVar_hsa_circ_136610,RMVar_hsa_circ_363166,RMVar_hsa_circ_285466,RMVar_hsa_circ_61432,RMVar_hsa_circ_332675,RMVar_hsa_circ_136612,RMVar_hsa_circ_136613,RMVar_hsa_circ_343437,RMVar_hsa_circ_318341,RMVar_hsa_circ_298012,RMVar_hsa_circ_136616,RMVar_hsa_circ_136617,RMVar_hsa_circ_136618,RMVar_hsa_circ_136615 37037 RMVar_ID_37037 Human_SNP_ID_34683135 A-to-I Human chr1 - 155373808 155373808 155373808 AAAACATCAACTGGGCATGGTGGCGTGTGCCTATAGTCCCAGCTATTCTGGAGGCTGAGGTGAGA AAAACATCAACTGGGCATGGTGGCGTGTGCCTGTAGTCCCAGCTATTCTGGAGGCTGAGGTGAGA T C ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1023951371 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42667,RMVar_hsa_circ_368935,RMVar_hsa_circ_366827,RMVar_hsa_circ_358498,RMVar_hsa_circ_69363,RMVar_hsa_circ_55904,RMVar_hsa_circ_136579,RMVar_hsa_circ_91291,RMVar_hsa_circ_136577,RMVar_hsa_circ_370041,RMVar_hsa_circ_356619,RMVar_hsa_circ_91812,RMVar_hsa_circ_55595,RMVar_hsa_circ_136580,RMVar_hsa_circ_106304,RMVar_hsa_circ_67956,RMVar_hsa_circ_136588,RMVar_hsa_circ_107116,RMVar_hsa_circ_136592,RMVar_hsa_circ_78519,RMVar_hsa_circ_36517,RMVar_hsa_circ_71110,RMVar_hsa_circ_136595,RMVar_hsa_circ_136594,RMVar_hsa_circ_110760,RMVar_hsa_circ_97081,RMVar_hsa_circ_360900,RMVar_hsa_circ_136598,RMVar_hsa_circ_11734,RMVar_hsa_circ_136603,RMVar_hsa_circ_85679,RMVar_hsa_circ_42461,RMVar_hsa_circ_136606,RMVar_hsa_circ_55666,RMVar_hsa_circ_357101,RMVar_hsa_circ_118802,RMVar_hsa_circ_136607,RMVar_hsa_circ_22549,RMVar_hsa_circ_102723,RMVar_hsa_circ_59208,RMVar_hsa_circ_66639,RMVar_hsa_circ_136610,RMVar_hsa_circ_363166,RMVar_hsa_circ_285466,RMVar_hsa_circ_61432,RMVar_hsa_circ_332675,RMVar_hsa_circ_136612,RMVar_hsa_circ_136613,RMVar_hsa_circ_343437,RMVar_hsa_circ_318341,RMVar_hsa_circ_298012,RMVar_hsa_circ_136616,RMVar_hsa_circ_136617,RMVar_hsa_circ_136618,RMVar_hsa_circ_136615 37038 RMVar_ID_37038 Human_SNP_ID_34683583 A-to-I Human chr1 - 155375759 155375759 155375759 AGTTTCATTCTCGTTGCCCAGGCTGGAGTGCAATGGCACAATCTCAGCTCACTGCAGCCTCCACC AGTTTCATTCTCGTTGCCCAGGCTGGAGTGCAGTGGCACAATCTCAGCTCACTGCAGCCTCCACC T C ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1299307284 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42667,RMVar_hsa_circ_368935,RMVar_hsa_circ_366827,RMVar_hsa_circ_358498,RMVar_hsa_circ_69363,RMVar_hsa_circ_55904,RMVar_hsa_circ_136579,RMVar_hsa_circ_91291,RMVar_hsa_circ_136577,RMVar_hsa_circ_370041,RMVar_hsa_circ_356619,RMVar_hsa_circ_91812,RMVar_hsa_circ_55595,RMVar_hsa_circ_136580,RMVar_hsa_circ_106304,RMVar_hsa_circ_67956,RMVar_hsa_circ_136588,RMVar_hsa_circ_107116,RMVar_hsa_circ_136592,RMVar_hsa_circ_78519,RMVar_hsa_circ_36517,RMVar_hsa_circ_71110,RMVar_hsa_circ_136595,RMVar_hsa_circ_136594,RMVar_hsa_circ_110760,RMVar_hsa_circ_97081,RMVar_hsa_circ_360900,RMVar_hsa_circ_136598,RMVar_hsa_circ_11734,RMVar_hsa_circ_136603,RMVar_hsa_circ_85679,RMVar_hsa_circ_42461,RMVar_hsa_circ_136606,RMVar_hsa_circ_55666,RMVar_hsa_circ_357101,RMVar_hsa_circ_118802,RMVar_hsa_circ_136607,RMVar_hsa_circ_22549,RMVar_hsa_circ_102723,RMVar_hsa_circ_59208,RMVar_hsa_circ_66639,RMVar_hsa_circ_136610,RMVar_hsa_circ_363166,RMVar_hsa_circ_285466,RMVar_hsa_circ_61432,RMVar_hsa_circ_332675,RMVar_hsa_circ_136612,RMVar_hsa_circ_136613,RMVar_hsa_circ_343437,RMVar_hsa_circ_318341,RMVar_hsa_circ_298012,RMVar_hsa_circ_136616,RMVar_hsa_circ_136617,RMVar_hsa_circ_136618,RMVar_hsa_circ_136615 37039 RMVar_ID_37039 Human_SNP_ID_34683945 A-to-I Human chr1 - 155377179 155377179 155377179 GAATTTGGCTGGCATGGTGGCTCATGCCTATAATCCAAGCACTTTGGGAGGCTGAGGCAGGCAGG GAATTTGGCTGGCATGGTGGCTCATGCCTATAGTCCAAGCACTTTGGGAGGCTGAGGCAGGCAGG T C ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1253890734 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42667,RMVar_hsa_circ_368935,RMVar_hsa_circ_366827,RMVar_hsa_circ_358498,RMVar_hsa_circ_69363,RMVar_hsa_circ_55904,RMVar_hsa_circ_136579,RMVar_hsa_circ_91291,RMVar_hsa_circ_136577,RMVar_hsa_circ_370041,RMVar_hsa_circ_356619,RMVar_hsa_circ_91812,RMVar_hsa_circ_55595,RMVar_hsa_circ_136580,RMVar_hsa_circ_106304,RMVar_hsa_circ_67956,RMVar_hsa_circ_136588,RMVar_hsa_circ_107116,RMVar_hsa_circ_136592,RMVar_hsa_circ_78519,RMVar_hsa_circ_36517,RMVar_hsa_circ_71110,RMVar_hsa_circ_136595,RMVar_hsa_circ_136594,RMVar_hsa_circ_110760,RMVar_hsa_circ_97081,RMVar_hsa_circ_360900,RMVar_hsa_circ_136598,RMVar_hsa_circ_11734,RMVar_hsa_circ_136603,RMVar_hsa_circ_85679,RMVar_hsa_circ_42461,RMVar_hsa_circ_136606,RMVar_hsa_circ_55666,RMVar_hsa_circ_357101,RMVar_hsa_circ_118802,RMVar_hsa_circ_136607,RMVar_hsa_circ_22549,RMVar_hsa_circ_102723,RMVar_hsa_circ_59208,RMVar_hsa_circ_66639,RMVar_hsa_circ_136610,RMVar_hsa_circ_363166,RMVar_hsa_circ_285466,RMVar_hsa_circ_61432,RMVar_hsa_circ_332675,RMVar_hsa_circ_136612,RMVar_hsa_circ_136613,RMVar_hsa_circ_343437,RMVar_hsa_circ_318341,RMVar_hsa_circ_298012,RMVar_hsa_circ_136616,RMVar_hsa_circ_136617,RMVar_hsa_circ_136618,RMVar_hsa_circ_136615 37040 RMVar_ID_37040 Human_SNP_ID_34684094 A-to-I Human chr1 - 155377832 155377832 155377832 TATTTTTAGTAGAGATGGGATTTCACCGTATTAGCCAGGATGATCTCAATCTGACCTCGTGATCC TATTTTTAGTAGAGATGGGATTTCACCGTATTCGCCAGGATGATCTCAATCTGACCTCGTGATCC T G ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1480279914 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42667,RMVar_hsa_circ_368935,RMVar_hsa_circ_366827,RMVar_hsa_circ_358498,RMVar_hsa_circ_69363,RMVar_hsa_circ_55904,RMVar_hsa_circ_136579,RMVar_hsa_circ_91291,RMVar_hsa_circ_136577,RMVar_hsa_circ_370041,RMVar_hsa_circ_356619,RMVar_hsa_circ_91812,RMVar_hsa_circ_55595,RMVar_hsa_circ_136580,RMVar_hsa_circ_106304,RMVar_hsa_circ_67956,RMVar_hsa_circ_136588,RMVar_hsa_circ_107116,RMVar_hsa_circ_136592,RMVar_hsa_circ_78519,RMVar_hsa_circ_36517,RMVar_hsa_circ_71110,RMVar_hsa_circ_136595,RMVar_hsa_circ_136594,RMVar_hsa_circ_110760,RMVar_hsa_circ_97081,RMVar_hsa_circ_360900,RMVar_hsa_circ_136598,RMVar_hsa_circ_11734,RMVar_hsa_circ_136603,RMVar_hsa_circ_85679,RMVar_hsa_circ_42461,RMVar_hsa_circ_136606,RMVar_hsa_circ_55666,RMVar_hsa_circ_357101,RMVar_hsa_circ_118802,RMVar_hsa_circ_136607,RMVar_hsa_circ_22549,RMVar_hsa_circ_102723,RMVar_hsa_circ_59208,RMVar_hsa_circ_66639,RMVar_hsa_circ_136610,RMVar_hsa_circ_363166,RMVar_hsa_circ_285466,RMVar_hsa_circ_61432,RMVar_hsa_circ_332675,RMVar_hsa_circ_136612,RMVar_hsa_circ_136613,RMVar_hsa_circ_343437,RMVar_hsa_circ_318341,RMVar_hsa_circ_298012,RMVar_hsa_circ_136616,RMVar_hsa_circ_136617,RMVar_hsa_circ_136618,RMVar_hsa_circ_136615 37041 RMVar_ID_37041 Human_SNP_ID_34684101 A-to-I Human chr1 - 155377854 155377854 155377854 CACACCCAGCTAATTTTTTTTGTATTTTTAGTAGAGATGGGATTTCACCGTATTAGCCAGGATGA CACACCCAGCTAATTTTTTTTGTATTTTTAGTGGAGATGGGATTTCACCGTATTAGCCAGGATGA T C ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1186853322 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42667,RMVar_hsa_circ_368935,RMVar_hsa_circ_366827,RMVar_hsa_circ_358498,RMVar_hsa_circ_69363,RMVar_hsa_circ_55904,RMVar_hsa_circ_136579,RMVar_hsa_circ_91291,RMVar_hsa_circ_136577,RMVar_hsa_circ_370041,RMVar_hsa_circ_356619,RMVar_hsa_circ_91812,RMVar_hsa_circ_55595,RMVar_hsa_circ_136580,RMVar_hsa_circ_106304,RMVar_hsa_circ_67956,RMVar_hsa_circ_136588,RMVar_hsa_circ_107116,RMVar_hsa_circ_136592,RMVar_hsa_circ_78519,RMVar_hsa_circ_36517,RMVar_hsa_circ_71110,RMVar_hsa_circ_136595,RMVar_hsa_circ_136594,RMVar_hsa_circ_110760,RMVar_hsa_circ_97081,RMVar_hsa_circ_360900,RMVar_hsa_circ_136598,RMVar_hsa_circ_11734,RMVar_hsa_circ_136603,RMVar_hsa_circ_85679,RMVar_hsa_circ_42461,RMVar_hsa_circ_136606,RMVar_hsa_circ_55666,RMVar_hsa_circ_357101,RMVar_hsa_circ_118802,RMVar_hsa_circ_136607,RMVar_hsa_circ_22549,RMVar_hsa_circ_102723,RMVar_hsa_circ_59208,RMVar_hsa_circ_66639,RMVar_hsa_circ_136610,RMVar_hsa_circ_363166,RMVar_hsa_circ_285466,RMVar_hsa_circ_61432,RMVar_hsa_circ_332675,RMVar_hsa_circ_136612,RMVar_hsa_circ_136613,RMVar_hsa_circ_343437,RMVar_hsa_circ_318341,RMVar_hsa_circ_298012,RMVar_hsa_circ_136616,RMVar_hsa_circ_136617,RMVar_hsa_circ_136618,RMVar_hsa_circ_136615 37042 RMVar_ID_37042 Human_SNP_ID_34686849 A-to-I Human chr1 - 155389166 155389166 155389166 TGGTCTCTACTAAAAATAGAAAAAAATTAGCCAGGAGTGATAGTGGATGCCTGTAATCCCAGTTA TGGTCTCTACTAAAAATAGAAAAAAATTAGCCGGGAGTGATAGTGGATGCCTGTAATCCCAGTTA T C ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417301839 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42667,RMVar_hsa_circ_368935,RMVar_hsa_circ_366827,RMVar_hsa_circ_358498,RMVar_hsa_circ_69363,RMVar_hsa_circ_136579,RMVar_hsa_circ_91291,RMVar_hsa_circ_136577,RMVar_hsa_circ_370041,RMVar_hsa_circ_356619,RMVar_hsa_circ_91812,RMVar_hsa_circ_55595,RMVar_hsa_circ_136580,RMVar_hsa_circ_106304,RMVar_hsa_circ_67956,RMVar_hsa_circ_136588,RMVar_hsa_circ_78519,RMVar_hsa_circ_36517,RMVar_hsa_circ_71110,RMVar_hsa_circ_136595,RMVar_hsa_circ_136594,RMVar_hsa_circ_110760,RMVar_hsa_circ_97081,RMVar_hsa_circ_360900,RMVar_hsa_circ_136598,RMVar_hsa_circ_11734,RMVar_hsa_circ_136603,RMVar_hsa_circ_85679,RMVar_hsa_circ_42461,RMVar_hsa_circ_136606,RMVar_hsa_circ_55666,RMVar_hsa_circ_357101,RMVar_hsa_circ_118802,RMVar_hsa_circ_136607,RMVar_hsa_circ_102723,RMVar_hsa_circ_59208,RMVar_hsa_circ_66639,RMVar_hsa_circ_136610,RMVar_hsa_circ_363166,RMVar_hsa_circ_285466,RMVar_hsa_circ_136612,RMVar_hsa_circ_136613,RMVar_hsa_circ_343437,RMVar_hsa_circ_318341,RMVar_hsa_circ_298012,RMVar_hsa_circ_96092,RMVar_hsa_circ_136616,RMVar_hsa_circ_136617,RMVar_hsa_circ_136618,RMVar_hsa_circ_326638,RMVar_hsa_circ_358840,RMVar_hsa_circ_326051,RMVar_hsa_circ_280559,RMVar_hsa_circ_136620,RMVar_hsa_circ_136622,RMVar_hsa_circ_136621,RMVar_hsa_circ_65665,RMVar_hsa_circ_136624 37043 RMVar_ID_37043 Human_SNP_ID_34687500 A-to-I Human chr1 - 155391783 155391777 155391783 CTTGGCTAATTTTTTGTACTTTTGATAAAGATAGGGTTTCACCATGTTGCTCAGGCTAGTCTCAA CTTGGCTAATTTTTTGTACTTTTGATAAAGAT______TCACCATGTTGCTCAGGCTAGTCTCAA AAACCCT A ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1487968143 Functional Loss DEL dbSNP153 33..38 33 - - - RMVar_hsa_circ_42667,RMVar_hsa_circ_368935,RMVar_hsa_circ_366827,RMVar_hsa_circ_358498,RMVar_hsa_circ_69363,RMVar_hsa_circ_136579,RMVar_hsa_circ_91291,RMVar_hsa_circ_136577,RMVar_hsa_circ_370041,RMVar_hsa_circ_356619,RMVar_hsa_circ_91812,RMVar_hsa_circ_55595,RMVar_hsa_circ_136580,RMVar_hsa_circ_106304,RMVar_hsa_circ_67956,RMVar_hsa_circ_136588,RMVar_hsa_circ_78519,RMVar_hsa_circ_36517,RMVar_hsa_circ_71110,RMVar_hsa_circ_136595,RMVar_hsa_circ_136594,RMVar_hsa_circ_110760,RMVar_hsa_circ_97081,RMVar_hsa_circ_360900,RMVar_hsa_circ_136598,RMVar_hsa_circ_11734,RMVar_hsa_circ_136603,RMVar_hsa_circ_85679,RMVar_hsa_circ_42461,RMVar_hsa_circ_136606,RMVar_hsa_circ_55666,RMVar_hsa_circ_357101,RMVar_hsa_circ_118802,RMVar_hsa_circ_136607,RMVar_hsa_circ_102723,RMVar_hsa_circ_59208,RMVar_hsa_circ_66639,RMVar_hsa_circ_136610,RMVar_hsa_circ_363166,RMVar_hsa_circ_285466,RMVar_hsa_circ_136612,RMVar_hsa_circ_136613,RMVar_hsa_circ_343437,RMVar_hsa_circ_318341,RMVar_hsa_circ_298012,RMVar_hsa_circ_96092,RMVar_hsa_circ_136616,RMVar_hsa_circ_136617,RMVar_hsa_circ_136618,RMVar_hsa_circ_326638,RMVar_hsa_circ_358840,RMVar_hsa_circ_326051,RMVar_hsa_circ_280559,RMVar_hsa_circ_136620,RMVar_hsa_circ_136622,RMVar_hsa_circ_136621,RMVar_hsa_circ_65665,RMVar_hsa_circ_136624 37044 RMVar_ID_37044 Human_SNP_ID_34687502 A-to-I Human chr1 - 155391783 155391783 155391783 CTTGGCTAATTTTTTGTACTTTTGATAAAGATAGGGTTTCACCATGTTGCTCAGGCTAGTCTCAA CTTGGCTAATTTTTTGTACTTTTGATAAAGATGGGGTTTCACCATGTTGCTCAGGCTAGTCTCAA T C ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910598133 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42667,RMVar_hsa_circ_368935,RMVar_hsa_circ_366827,RMVar_hsa_circ_358498,RMVar_hsa_circ_69363,RMVar_hsa_circ_136579,RMVar_hsa_circ_91291,RMVar_hsa_circ_136577,RMVar_hsa_circ_370041,RMVar_hsa_circ_356619,RMVar_hsa_circ_91812,RMVar_hsa_circ_55595,RMVar_hsa_circ_136580,RMVar_hsa_circ_106304,RMVar_hsa_circ_67956,RMVar_hsa_circ_136588,RMVar_hsa_circ_78519,RMVar_hsa_circ_36517,RMVar_hsa_circ_71110,RMVar_hsa_circ_136595,RMVar_hsa_circ_136594,RMVar_hsa_circ_110760,RMVar_hsa_circ_97081,RMVar_hsa_circ_360900,RMVar_hsa_circ_136598,RMVar_hsa_circ_11734,RMVar_hsa_circ_136603,RMVar_hsa_circ_85679,RMVar_hsa_circ_42461,RMVar_hsa_circ_136606,RMVar_hsa_circ_55666,RMVar_hsa_circ_357101,RMVar_hsa_circ_118802,RMVar_hsa_circ_136607,RMVar_hsa_circ_102723,RMVar_hsa_circ_59208,RMVar_hsa_circ_66639,RMVar_hsa_circ_136610,RMVar_hsa_circ_363166,RMVar_hsa_circ_285466,RMVar_hsa_circ_136612,RMVar_hsa_circ_136613,RMVar_hsa_circ_343437,RMVar_hsa_circ_318341,RMVar_hsa_circ_298012,RMVar_hsa_circ_96092,RMVar_hsa_circ_136616,RMVar_hsa_circ_136617,RMVar_hsa_circ_136618,RMVar_hsa_circ_326638,RMVar_hsa_circ_358840,RMVar_hsa_circ_326051,RMVar_hsa_circ_280559,RMVar_hsa_circ_136620,RMVar_hsa_circ_136622,RMVar_hsa_circ_136621,RMVar_hsa_circ_65665,RMVar_hsa_circ_136624 37045 RMVar_ID_37045 Human_SNP_ID_34688760 A-to-I Human chr1 - 155397246 155397246 155397246 GTGATCCACCCGCCTTGGCCTCCCACAGTGCTAGGATTGCAGGCATGAGCCACCCTGTCCGGTCA GTGATCCACCCGCCTTGGCCTCCCACAGTGCTGGGATTGCAGGCATGAGCCACCCTGTCCGGTCA T C ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1558062538 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10596101 RMVar_hsa_circ_368935,RMVar_hsa_circ_366827,RMVar_hsa_circ_358498,RMVar_hsa_circ_69363,RMVar_hsa_circ_136579,RMVar_hsa_circ_91291,RMVar_hsa_circ_136577,RMVar_hsa_circ_370041,RMVar_hsa_circ_91812,RMVar_hsa_circ_55595,RMVar_hsa_circ_136580,RMVar_hsa_circ_106304,RMVar_hsa_circ_136588,RMVar_hsa_circ_78519,RMVar_hsa_circ_36517,RMVar_hsa_circ_136595,RMVar_hsa_circ_136594,RMVar_hsa_circ_110760,RMVar_hsa_circ_97081,RMVar_hsa_circ_360900,RMVar_hsa_circ_136598,RMVar_hsa_circ_136603,RMVar_hsa_circ_85679,RMVar_hsa_circ_42461,RMVar_hsa_circ_136606,RMVar_hsa_circ_55666,RMVar_hsa_circ_118802,RMVar_hsa_circ_136607,RMVar_hsa_circ_102723,RMVar_hsa_circ_59208,RMVar_hsa_circ_66639,RMVar_hsa_circ_136610,RMVar_hsa_circ_363166,RMVar_hsa_circ_136613,RMVar_hsa_circ_343437,RMVar_hsa_circ_318341,RMVar_hsa_circ_96092,RMVar_hsa_circ_136617,RMVar_hsa_circ_136618,RMVar_hsa_circ_326638,RMVar_hsa_circ_358840,RMVar_hsa_circ_280559,RMVar_hsa_circ_136620,RMVar_hsa_circ_136621,RMVar_hsa_circ_65665,RMVar_hsa_circ_136625,RMVar_hsa_circ_53527,RMVar_hsa_circ_275389,RMVar_hsa_circ_136624,RMVar_hsa_circ_304435,RMVar_hsa_circ_270411,RMVar_hsa_circ_136627,RMVar_hsa_circ_136628,RMVar_hsa_circ_136626 37046 RMVar_ID_37046 Human_SNP_ID_34689149 A-to-I Human chr1 - 155398960 155398960 155398960 GGGAGGCCAGGGCAGGCAAGTCGCTTGAGCCCAGGAGTTGAAGACCAGCCTGGGCAACATGGTGA GGGAGGCCAGGGCAGGCAAGTCGCTTGAGCCCGGGAGTTGAAGACCAGCCTGGGCAACATGGTGA T C ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs905435862 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_368935,RMVar_hsa_circ_366827,RMVar_hsa_circ_358498,RMVar_hsa_circ_69363,RMVar_hsa_circ_136579,RMVar_hsa_circ_91291,RMVar_hsa_circ_136577,RMVar_hsa_circ_370041,RMVar_hsa_circ_91812,RMVar_hsa_circ_55595,RMVar_hsa_circ_136580,RMVar_hsa_circ_106304,RMVar_hsa_circ_136588,RMVar_hsa_circ_78519,RMVar_hsa_circ_36517,RMVar_hsa_circ_136595,RMVar_hsa_circ_136594,RMVar_hsa_circ_110760,RMVar_hsa_circ_97081,RMVar_hsa_circ_360900,RMVar_hsa_circ_136598,RMVar_hsa_circ_136603,RMVar_hsa_circ_85679,RMVar_hsa_circ_42461,RMVar_hsa_circ_136606,RMVar_hsa_circ_55666,RMVar_hsa_circ_118802,RMVar_hsa_circ_136607,RMVar_hsa_circ_102723,RMVar_hsa_circ_59208,RMVar_hsa_circ_66639,RMVar_hsa_circ_136610,RMVar_hsa_circ_363166,RMVar_hsa_circ_136613,RMVar_hsa_circ_343437,RMVar_hsa_circ_318341,RMVar_hsa_circ_96092,RMVar_hsa_circ_136617,RMVar_hsa_circ_136618,RMVar_hsa_circ_326638,RMVar_hsa_circ_358840,RMVar_hsa_circ_280559,RMVar_hsa_circ_136620,RMVar_hsa_circ_136621,RMVar_hsa_circ_65665,RMVar_hsa_circ_136625,RMVar_hsa_circ_53527,RMVar_hsa_circ_275389,RMVar_hsa_circ_136624,RMVar_hsa_circ_304435,RMVar_hsa_circ_270411,RMVar_hsa_circ_136627,RMVar_hsa_circ_136628,RMVar_hsa_circ_136626 37047 RMVar_ID_37047 Human_SNP_ID_34690359 A-to-I Human chr1 - 155404296 155404296 155404296 ACTAGAGTACAGTGGCATAATACCAGCTCACTACAGTCTCCACCTCCTAGACTCAAGCGTTCATC ACTAGAGTACAGTGGCATAATACCAGCTCACTGCAGTCTCCACCTCCTAGACTCAAGCGTTCATC T C ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1052806269 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_368935,RMVar_hsa_circ_366827,RMVar_hsa_circ_358498,RMVar_hsa_circ_69363,RMVar_hsa_circ_136579,RMVar_hsa_circ_91291,RMVar_hsa_circ_136577,RMVar_hsa_circ_370041,RMVar_hsa_circ_91812,RMVar_hsa_circ_55595,RMVar_hsa_circ_136580,RMVar_hsa_circ_106304,RMVar_hsa_circ_136588,RMVar_hsa_circ_78519,RMVar_hsa_circ_36517,RMVar_hsa_circ_136595,RMVar_hsa_circ_136594,RMVar_hsa_circ_110760,RMVar_hsa_circ_97081,RMVar_hsa_circ_360900,RMVar_hsa_circ_136598,RMVar_hsa_circ_136603,RMVar_hsa_circ_85679,RMVar_hsa_circ_42461,RMVar_hsa_circ_136606,RMVar_hsa_circ_55666,RMVar_hsa_circ_118802,RMVar_hsa_circ_136607,RMVar_hsa_circ_102723,RMVar_hsa_circ_59208,RMVar_hsa_circ_66639,RMVar_hsa_circ_136610,RMVar_hsa_circ_363166,RMVar_hsa_circ_136613,RMVar_hsa_circ_343437,RMVar_hsa_circ_318341,RMVar_hsa_circ_96092,RMVar_hsa_circ_136617,RMVar_hsa_circ_136618,RMVar_hsa_circ_326638,RMVar_hsa_circ_358840,RMVar_hsa_circ_280559,RMVar_hsa_circ_136620,RMVar_hsa_circ_136621,RMVar_hsa_circ_65665,RMVar_hsa_circ_53527,RMVar_hsa_circ_275389,RMVar_hsa_circ_136624,RMVar_hsa_circ_304435,RMVar_hsa_circ_270411,RMVar_hsa_circ_136627,RMVar_hsa_circ_136628,RMVar_hsa_circ_136626 37048 RMVar_ID_37048 Human_SNP_ID_34691803 A-to-I Human chr1 - 155410265 155410265 155410265 AAAATCCAGCAGGTGTGGTGGCGCACAGCTGTAGTCCCAGCTGCTTGTGAGACTGAAGTGAGCAG AAAATCCAGCAGGTGTGGTGGCGCACAGCTGTCGTCCCAGCTGCTTGTGAGACTGAAGTGAGCAG T G ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs889343430 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_368935,RMVar_hsa_circ_366827,RMVar_hsa_circ_358498,RMVar_hsa_circ_69363,RMVar_hsa_circ_136579,RMVar_hsa_circ_91291,RMVar_hsa_circ_136577,RMVar_hsa_circ_370041,RMVar_hsa_circ_91812,RMVar_hsa_circ_55595,RMVar_hsa_circ_136580,RMVar_hsa_circ_106304,RMVar_hsa_circ_136588,RMVar_hsa_circ_78519,RMVar_hsa_circ_36517,RMVar_hsa_circ_136595,RMVar_hsa_circ_136594,RMVar_hsa_circ_110760,RMVar_hsa_circ_97081,RMVar_hsa_circ_360900,RMVar_hsa_circ_136598,RMVar_hsa_circ_136603,RMVar_hsa_circ_85679,RMVar_hsa_circ_42461,RMVar_hsa_circ_136606,RMVar_hsa_circ_55666,RMVar_hsa_circ_118802,RMVar_hsa_circ_136607,RMVar_hsa_circ_102723,RMVar_hsa_circ_59208,RMVar_hsa_circ_66639,RMVar_hsa_circ_136610,RMVar_hsa_circ_363166,RMVar_hsa_circ_136613,RMVar_hsa_circ_343437,RMVar_hsa_circ_318341,RMVar_hsa_circ_96092,RMVar_hsa_circ_136617,RMVar_hsa_circ_136618,RMVar_hsa_circ_326638,RMVar_hsa_circ_358840,RMVar_hsa_circ_280559,RMVar_hsa_circ_136620,RMVar_hsa_circ_136621,RMVar_hsa_circ_65665,RMVar_hsa_circ_53527,RMVar_hsa_circ_275389,RMVar_hsa_circ_136624,RMVar_hsa_circ_304435,RMVar_hsa_circ_270411,RMVar_hsa_circ_136627,RMVar_hsa_circ_136628,RMVar_hsa_circ_136626,RMVar_hsa_circ_136629,RMVar_hsa_circ_115859 37049 RMVar_ID_37049 Human_SNP_ID_34695293 A-to-I Human chr1 - 155423507 155423507 155423507 TGGAGTGCGGTGGCACGATCTTGGCTCACTGCAACCTCTGCCTCCCGGGTTCCAGCAATTCCCCG TGGAGTGCGGTGGCACGATCTTGGCTCACTGCGACCTCTGCCTCCCGGGTTCCAGCAATTCCCCG T C ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1339864163 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_366827,RMVar_hsa_circ_358498,RMVar_hsa_circ_69363,RMVar_hsa_circ_136579,RMVar_hsa_circ_91291,RMVar_hsa_circ_136577,RMVar_hsa_circ_370041,RMVar_hsa_circ_55595,RMVar_hsa_circ_106304,RMVar_hsa_circ_136588,RMVar_hsa_circ_78519,RMVar_hsa_circ_36517,RMVar_hsa_circ_136594,RMVar_hsa_circ_97081,RMVar_hsa_circ_136598,RMVar_hsa_circ_85679,RMVar_hsa_circ_136606,RMVar_hsa_circ_118802,RMVar_hsa_circ_136607,RMVar_hsa_circ_102723,RMVar_hsa_circ_59208,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_326638,RMVar_hsa_circ_358840,RMVar_hsa_circ_136620,RMVar_hsa_circ_65665,RMVar_hsa_circ_136631,RMVar_hsa_circ_53527,RMVar_hsa_circ_136624,RMVar_hsa_circ_304435,RMVar_hsa_circ_270411,RMVar_hsa_circ_136627,RMVar_hsa_circ_136628,RMVar_hsa_circ_291805,RMVar_hsa_circ_350393,RMVar_hsa_circ_363917,RMVar_hsa_circ_277790,RMVar_hsa_circ_136632 37050 RMVar_ID_37050 Human_SNP_ID_34697261 A-to-I Human chr1 - 155431169 155431169 155431169 ACGGCATCTTGCTCTGTTGCCCAGGCTGGAGTACAATGGCTTGGCTCACTGCAACCTCCACCTCT ACGGCATCTTGCTCTGTTGCCCAGGCTGGAGTGCAATGGCTTGGCTCACTGCAACCTCCACCTCT T C ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1034298259 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_366827,RMVar_hsa_circ_358498,RMVar_hsa_circ_69363,RMVar_hsa_circ_136579,RMVar_hsa_circ_91291,RMVar_hsa_circ_136577,RMVar_hsa_circ_370041,RMVar_hsa_circ_55595,RMVar_hsa_circ_106304,RMVar_hsa_circ_136588,RMVar_hsa_circ_78519,RMVar_hsa_circ_36517,RMVar_hsa_circ_136594,RMVar_hsa_circ_97081,RMVar_hsa_circ_136598,RMVar_hsa_circ_85679,RMVar_hsa_circ_136606,RMVar_hsa_circ_118802,RMVar_hsa_circ_136607,RMVar_hsa_circ_102723,RMVar_hsa_circ_59208,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_326638,RMVar_hsa_circ_358840,RMVar_hsa_circ_136620,RMVar_hsa_circ_65665,RMVar_hsa_circ_136631,RMVar_hsa_circ_53527,RMVar_hsa_circ_136624,RMVar_hsa_circ_304435,RMVar_hsa_circ_270411,RMVar_hsa_circ_136627,RMVar_hsa_circ_136628,RMVar_hsa_circ_291805,RMVar_hsa_circ_350393,RMVar_hsa_circ_363917,RMVar_hsa_circ_277790,RMVar_hsa_circ_136632 37051 RMVar_ID_37051 Human_SNP_ID_34701810 A-to-I Human chr1 - 155448322 155448322 155448322 CAACAACAAAACGAAAAGAAAAATAAAAATTAACCCAGAATAGCCAAAGCTATTTCTAAGCTGAA CAACAACAAAACGAAAAGAAAAATAAAAATTAGCCCAGAATAGCCAAAGCTATTTCTAAGCTGAA T C ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10752610 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_4064 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 37052 RMVar_ID_37052 Human_SNP_ID_34702598 A-to-I Human chr1 - 155451647 155451647 155451647 TACAAGCGATTCTCCTGCCTCAGCCTCCAAGTAACTGGGATTACAGGTGTCCACCACCACGCCAG TACAAGCGATTCTCCTGCCTCAGCCTCCAAGTTACTGGGATTACAGGTGTCCACCACCACGCCAG T A ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1250952135 Functional Loss SNV dbSNP153 33..33 33 - - - 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 37053 RMVar_ID_37053 Human_SNP_ID_34702882 A-to-I Human chr1 - 155452799 155452799 155452799 TTATCCCAGCACATTGGGAGACCAAGGCGGGTAGATCACTTGAGGCCAGGAGTTCGAGGGCAGCC TTATCCCAGCACATTGGGAGACCAAGGCGGGTGGATCACTTGAGGCCAGGAGTTCGAGGGCAGCC T C ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1163052880 Functional Loss SNV dbSNP153 33..33 33 - - - 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 37054 RMVar_ID_37054 Human_SNP_ID_34705369 A-to-I Human chr1 - 155463682 155463682 155463682 CAAGCGATCTTCCCACTTCAGCCTCCCAAGTAACTGGGACTACAGGGTATGCACCACTATGCCCA CAAGCGATCTTCCCACTTCAGCCTCCCAAGTAGCTGGGACTACAGGGTATGCACCACTATGCCCA T C ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1294917307 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69363,RMVar_hsa_circ_53527,RMVar_hsa_circ_350393,RMVar_hsa_circ_363917,RMVar_hsa_circ_322614,RMVar_hsa_circ_311449,RMVar_hsa_circ_136633,RMVar_hsa_circ_136639,RMVar_hsa_circ_281333,RMVar_hsa_circ_375532,RMVar_hsa_circ_136640 37055 RMVar_ID_37055 Human_SNP_ID_34706718 A-to-I Human chr1 - 155469323 155469323 155469323 CAAATAATAGCCGGACGTGGTGGCACATGCCTATAATCCCAGCTATTCAGGAGGCTGAGGCAGGA CAAATAATAGCCGGACGTGGTGGCACATGCCTGTAATCCCAGCTATTCAGGAGGCTGAGGCAGGA T C ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1182409438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5694645 RMVar_hsa_circ_69363,RMVar_hsa_circ_53527,RMVar_hsa_circ_350393,RMVar_hsa_circ_363917,RMVar_hsa_circ_322614,RMVar_hsa_circ_311449,RMVar_hsa_circ_136633,RMVar_hsa_circ_136639,RMVar_hsa_circ_281333,RMVar_hsa_circ_375532,RMVar_hsa_circ_136640 37056 RMVar_ID_37056 Human_SNP_ID_34706745 A-to-I Human chr1 - 155469456 155469456 155469456 TCAAGTGGGTGGACGTGGTGGCTCACGCCTGTAATCCCAGAACTTTGGGAGGCTGAGGCGGGCAG TCAAGTGGGTGGACGTGGTGGCTCACGCCTGTGATCCCAGAACTTTGGGAGGCTGAGGCGGGCAG T C ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1189878173 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69363,RMVar_hsa_circ_53527,RMVar_hsa_circ_350393,RMVar_hsa_circ_363917,RMVar_hsa_circ_322614,RMVar_hsa_circ_311449,RMVar_hsa_circ_136633,RMVar_hsa_circ_136639,RMVar_hsa_circ_281333,RMVar_hsa_circ_375532,RMVar_hsa_circ_136640 37057 RMVar_ID_37057 Human_SNP_ID_34707324 A-to-I Human chr1 - 155472106 155472106 155472106 TTGAATTTTTTGTAGAGTCGGGGTTTCACTGTATTGGCCAGGCTAGTTTCAAACTCCTGACCGCA TTGAATTTTTTGTAGAGTCGGGGTTTCACTGTGTTGGCCAGGCTAGTTTCAAACTCCTGACCGCA T C ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1157774418 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69363,RMVar_hsa_circ_53527,RMVar_hsa_circ_350393,RMVar_hsa_circ_363917,RMVar_hsa_circ_322614,RMVar_hsa_circ_311449,RMVar_hsa_circ_136633,RMVar_hsa_circ_136639,RMVar_hsa_circ_281333,RMVar_hsa_circ_375532,RMVar_hsa_circ_136640 37058 RMVar_ID_37058 Human_SNP_ID_34707332 A-to-I Human chr1 - 155472125 155472125 155472125 CACCACATTTGGCTAATTTTTGAATTTTTTGTAGAGTCGGGGTTTCACTGTATTGGCCAGGCTAG CACCACATTTGGCTAATTTTTGAATTTTTTGTGGAGTCGGGGTTTCACTGTATTGGCCAGGCTAG T C ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025993836 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10597127 RMVar_hsa_circ_69363,RMVar_hsa_circ_53527,RMVar_hsa_circ_350393,RMVar_hsa_circ_363917,RMVar_hsa_circ_322614,RMVar_hsa_circ_311449,RMVar_hsa_circ_136633,RMVar_hsa_circ_136639,RMVar_hsa_circ_281333,RMVar_hsa_circ_375532,RMVar_hsa_circ_136640 37059 RMVar_ID_37059 Human_SNP_ID_34707374 A-to-I Human chr1 - 155472297 155472297 155472297 ACGAATTTGTCTTTTTAAAAATTTCCTTCTTTATTTATTTGAGATGGAGTCTCTCTCTGTCATCC ACGAATTTGTCTTTTTAAAAATTTCCTTCTTTCTTTATTTGAGATGGAGTCTCTCTCTGTCATCC T G ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1182158080 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5694653,Human_RBP_ID_10597130 RMVar_hsa_circ_69363,RMVar_hsa_circ_53527,RMVar_hsa_circ_350393,RMVar_hsa_circ_363917,RMVar_hsa_circ_322614,RMVar_hsa_circ_311449,RMVar_hsa_circ_136633,RMVar_hsa_circ_136639,RMVar_hsa_circ_281333,RMVar_hsa_circ_375532,RMVar_hsa_circ_136640 37060 RMVar_ID_37060 Human_SNP_ID_34707701 A-to-I Human chr1 - 155473700 155473700 155473700 GCCTAGGAGTTGAAGACCAGCCTGGGCAACATAGGAGCCTCCCATCTCTACAGAAAAATGTTTTT GCCTAGGAGTTGAAGACCAGCCTGGGCAACATGGGAGCCTCCCATCTCTACAGAAAAATGTTTTT T C ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1425765396 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69363,RMVar_hsa_circ_53527,RMVar_hsa_circ_350393,RMVar_hsa_circ_363917,RMVar_hsa_circ_322614,RMVar_hsa_circ_311449,RMVar_hsa_circ_136633,RMVar_hsa_circ_136639,RMVar_hsa_circ_281333,RMVar_hsa_circ_375532,RMVar_hsa_circ_136640 37061 RMVar_ID_37061 Human_SNP_ID_34707773 A-to-I Human chr1 - 155474017 155474017 155474017 CCAGCCTGGCCAACATGGCGAAACCTGTCTCTACTAAAATAAAAAAATTAGCCAGCAGTGCTGGT CCAGCCTGGCCAACATGGCGAAACCTGTCTCTGCTAAAATAAAAAAATTAGCCAGCAGTGCTGGT T C ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1244990970 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24752657 RMVar_hsa_circ_69363,RMVar_hsa_circ_53527,RMVar_hsa_circ_350393,RMVar_hsa_circ_363917,RMVar_hsa_circ_322614,RMVar_hsa_circ_311449,RMVar_hsa_circ_136633,RMVar_hsa_circ_136639,RMVar_hsa_circ_281333,RMVar_hsa_circ_375532,RMVar_hsa_circ_136640 37062 RMVar_ID_37062 Human_SNP_ID_34707878 A-to-I Human chr1 - 155474468 155474468 155474468 TCTTGAACTCCTGGGCTCAAAGGGACCCTCCTACCTTGCCCTCCCAAAGTGCTGGGATTATAGGC TCTTGAACTCCTGGGCTCAAAGGGACCCTCCTGCCTTGCCCTCCCAAAGTGCTGGGATTATAGGC T C ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs967174480 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69363,RMVar_hsa_circ_53527,RMVar_hsa_circ_350393,RMVar_hsa_circ_363917,RMVar_hsa_circ_322614,RMVar_hsa_circ_311449,RMVar_hsa_circ_136633,RMVar_hsa_circ_136639,RMVar_hsa_circ_281333,RMVar_hsa_circ_375532,RMVar_hsa_circ_136640 37063 RMVar_ID_37063 Human_SNP_ID_34707900 A-to-I Human chr1 - 155474552 155474552 155474552 GGACTACAGGTGCAAGCCACCAATGCCAGGCTAATTTCTTTGTATTTTTGTAGAGATGGGGTTTC GGACTACAGGTGCAAGCCACCAATGCCAGGCTGATTTCTTTGTATTTTTGTAGAGATGGGGTTTC T C ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs907927282 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69363,RMVar_hsa_circ_53527,RMVar_hsa_circ_350393,RMVar_hsa_circ_363917,RMVar_hsa_circ_322614,RMVar_hsa_circ_311449,RMVar_hsa_circ_136633,RMVar_hsa_circ_136639,RMVar_hsa_circ_281333,RMVar_hsa_circ_375532,RMVar_hsa_circ_136640 37064 RMVar_ID_37064 Human_SNP_ID_34707928 A-to-I Human chr1 - 155474636 155474636 155474636 GGAGTGCAGTGGCACGATCTTGGCTCACTGCAACCTGTTTCCTGGGCTCAAGCCATTTTCCAGCC GGAGTGCAGTGGCACGATCTTGGCTCACTGCAGCCTGTTTCCTGGGCTCAAGCCATTTTCCAGCC T C ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1026754649 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69363,RMVar_hsa_circ_53527,RMVar_hsa_circ_350393,RMVar_hsa_circ_363917,RMVar_hsa_circ_322614,RMVar_hsa_circ_311449,RMVar_hsa_circ_136633,RMVar_hsa_circ_136639,RMVar_hsa_circ_281333,RMVar_hsa_circ_375532,RMVar_hsa_circ_136640 37065 RMVar_ID_37065 Human_SNP_ID_34707929 A-to-I Human chr1 - 155474636 155474636 155474636 GGAGTGCAGTGGCACGATCTTGGCTCACTGCAACCTGTTTCCTGGGCTCAAGCCATTTTCCAGCC GGAGTGCAGTGGCACGATCTTGGCTCACTGCACCCTGTTTCCTGGGCTCAAGCCATTTTCCAGCC T G ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1026754649 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69363,RMVar_hsa_circ_53527,RMVar_hsa_circ_350393,RMVar_hsa_circ_363917,RMVar_hsa_circ_322614,RMVar_hsa_circ_311449,RMVar_hsa_circ_136633,RMVar_hsa_circ_136639,RMVar_hsa_circ_281333,RMVar_hsa_circ_375532,RMVar_hsa_circ_136640 37066 RMVar_ID_37066 Human_SNP_ID_34708092 A-to-I Human chr1 - 155475248 155475248 155475248 CCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCAGGAGGCGGAGATT CCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCGGGAGAATCGCTTGAACCCAGGAGGCGGAGATT T C ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs954885260 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69363,RMVar_hsa_circ_53527,RMVar_hsa_circ_350393,RMVar_hsa_circ_363917,RMVar_hsa_circ_322614,RMVar_hsa_circ_311449,RMVar_hsa_circ_136633,RMVar_hsa_circ_136639,RMVar_hsa_circ_281333,RMVar_hsa_circ_375532,RMVar_hsa_circ_136640 37067 RMVar_ID_37067 Human_SNP_ID_34715611 A-to-I Human chr1 - 155503798 155503798 155503798 ATCACTTGAGCACAGGAGGTCGAGGCTGCAGTAAGTTGTGTTCATGCCACTGTACTGCAGCCTAG ATCACTTGAGCACAGGAGGTCGAGGCTGCAGTGAGTTGTGTTCATGCCACTGTACTGCAGCCTAG T C ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1365634623 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10597597 RMVar_hsa_circ_363917,RMVar_hsa_circ_311449,RMVar_hsa_circ_375532,RMVar_hsa_circ_136640,RMVar_hsa_circ_136642,RMVar_hsa_circ_277354 37068 RMVar_ID_37068 Human_SNP_ID_34715635 A-to-I Human chr1 - 155503898 155503898 155503898 GCAACATGGTGAAACCCCCCTGTACAAAAAATACAAATGTTAGCCAGGCATGGTGGCTTACACCT GCAACATGGTGAAACCCCCCTGTACAAAAAATGCAAATGTTAGCCAGGCATGGTGGCTTACACCT T C ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956817426 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_363917,RMVar_hsa_circ_311449,RMVar_hsa_circ_375532,RMVar_hsa_circ_136640,RMVar_hsa_circ_136642,RMVar_hsa_circ_277354 37069 RMVar_ID_37069 Human_SNP_ID_34717489 A-to-I Human chr1 - 155511776 155511776 155511776 AATCTTGCCGGGCGTGGTGGCTCACCCCTGTAATCCCAGCAGTTTAGGAGGCCAAGGTGGGTGGA AATCTTGCCGGGCGTGGTGGCTCACCCCTGTAGTCCCAGCAGTTTAGGAGGCCAAGGTGGGTGGA T C ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1558180387 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_363917,RMVar_hsa_circ_311449,RMVar_hsa_circ_375532,RMVar_hsa_circ_136640,RMVar_hsa_circ_136642,RMVar_hsa_circ_277354 37070 RMVar_ID_37070 Human_SNP_ID_34719499 A-to-I Human chr1 - 155519838 155519838 155519838 CGTGGCCAACATGATGAAACCCCGTCTCTACTAAAAATACAAAAAATTAGCCAACCATGATGGCA CGTGGCCAACATGATGAAACCCCGTCTCTACTGAAAATACAAAAAATTAGCCAACCATGATGGCA T C ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1241332170 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_363917,RMVar_hsa_circ_311449,RMVar_hsa_circ_375532,RMVar_hsa_circ_136640,RMVar_hsa_circ_136642,RMVar_hsa_circ_277354 37071 RMVar_ID_37071 Human_SNP_ID_34719518 A-to-I Human chr1 - 155519945 155519945 155519945 TGGTAATATCGAATGTACTTGCCGGGCGTGGTAGCTCACGCCTGTAATCCCAGCACTTTGGCATG TGGTAATATCGAATGTACTTGCCGGGCGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGCATG T C ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1425535332 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_363917,RMVar_hsa_circ_311449,RMVar_hsa_circ_375532,RMVar_hsa_circ_136640,RMVar_hsa_circ_136642,RMVar_hsa_circ_277354 37072 RMVar_ID_37072 Human_SNP_ID_34721521 A-to-I Human chr1 - 155527572 155527572 155527572 TGATTGTGCCACTGCACTCTGGCCAGGGTGACAGAGAGAGACCTTGACTCAAAAAAAAAAAAAAA TGATTGTGCCACTGCACTCTGGCCAGGGTGACGGAGAGAGACCTTGACTCAAAAAAAAAAAAAAA T C ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1400936514 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10598052 37073 RMVar_ID_37073 Human_SNP_ID_34724324 A-to-I Human chr1 - 155538486 155538486 155538486 GGATGTGGTGGTGCGTTCCTGTAGTCCCGGCTACTCGGGAGGCTGAGGCAGGAGACTCGCTTGAA GGATGTGGTGGTGCGTTCCTGTAGTCCCGGCTGCTCGGGAGGCTGAGGCAGGAGACTCGCTTGAA T C ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1219424107 Functional Loss SNV dbSNP153 33..33 33 - - - 37074 RMVar_ID_37074 Human_SNP_ID_34725679 A-to-I Human chr1 - 155543839 155543839 155543839 GCCTCAACCTCCCGGGCTCAATTGATTCTTCTACCTCAGCCCCTGCCAAGTAGCTGGGACTACAG GCCTCAACCTCCCGGGCTCAATTGATTCTTCTCCCTCAGCCCCTGCCAAGTAGCTGGGACTACAG T G ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1212915626 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10598421,Human_RBP_ID_17558014 37075 RMVar_ID_37075 Human_SNP_ID_34725844 A-to-I Human chr1 - 155544468 155544468 155544468 CCTGGCTAACACGGTGAAACCCCATCTCTACTAAAAATACAAAAAAATTGGCTGGTCGTGGTTGC CCTGGCTAACACGGTGAAACCCCATCTCTACTGAAAATACAAAAAAATTGGCTGGTCGTGGTTGC T C ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs894998703 Functional Loss SNV dbSNP153 33..33 33 - - - 37076 RMVar_ID_37076 Human_SNP_ID_34726661 A-to-I Human chr1 - 155547179 155547179 155547179 TGGGAGGCCAAGGCGGGCAGATCACGAGGTCAAGAGATCTAAACCATCCTGGCCAACATGGTAAA TGGGAGGCCAAGGCGGGCAGATCACGAGGTCAGGAGATCTAAACCATCCTGGCCAACATGGTAAA T C ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1370800386 Functional Loss SNV dbSNP153 33..33 33 - - - 37077 RMVar_ID_37077 Human_SNP_ID_34727011 A-to-I Human chr1 - 155548487 155548487 155548487 ACGGAGTCTGGCTCTGTTGCCTAGGCTGGAGTACAATGGTGCCATCTAGGTTCACTGCAACCCCC ACGGAGTCTGGCTCTGTTGCCTAGGCTGGAGTGCAATGGTGCCATCTAGGTTCACTGCAACCCCC T C ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404246451 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_746280,Human_RBP_ID_10598481 37078 RMVar_ID_37078 Human_SNP_ID_34727223 A-to-I Human chr1 - 155549335 155549335 155549335 CTGTGTCTGGCCAAAAAGTTTTTTTTTGAGACAGGGTCTCTCTGTTATCCAGGCTAGAGTGCAGT CTGTGTCTGGCCAAAAAGTTTTTTTTTGAGACCGGGTCTCTCTGTTATCCAGGCTAGAGTGCAGT T G ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1437230946 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10598527 37079 RMVar_ID_37079 Human_SNP_ID_34727430 A-to-I Human chr1 - 155550054 155550052 155550054 ATTACGCCACGGCACTCCAGCTTGGGCAACAGAGCGAGACTCTGTCTCAAAAAAAAAAAGAGGCT ATTACGCCACGGCACTCCAGCTTGGGCAACAG__CGAGACTCTGTCTCAAAAAAAAAAAGAGGCT GCT G ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1234386829 Functional Loss DEL dbSNP153 33..34 33 - - - 37080 RMVar_ID_37080 Human_SNP_ID_34727612 A-to-I Human chr1 - 155550892 155550892 155550892 TTGAGCCCAGGAGGTCGAGGCTGCAGTCAGCCATGATTGCACCACTGCACTCTAGCCTGGGCAAC TTGAGCCCAGGAGGTCGAGGCTGCAGTCAGCCGTGATTGCACCACTGCACTCTAGCCTGGGCAAC T C ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1218039145 Functional Loss SNV dbSNP153 33..33 33 - - - 37081 RMVar_ID_37081 Human_SNP_ID_34728829 A-to-I Human chr1 - 155555031 155555031 155555031 TCAAGCGATTCTCCTGTTTGAGCCTCCTGAGTAGCTGGGACTACTGGTGTATGCCACCATGCCCG TCAAGCGATTCTCCTGTTTGAGCCTCCTGAGTTGCTGGGACTACTGGTGTATGCCACCATGCCCG T A ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1237588136 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24593253 37082 RMVar_ID_37082 Human_SNP_ID_34728830 A-to-I Human chr1 - 155555031 155555031 155555031 TCAAGCGATTCTCCTGTTTGAGCCTCCTGAGTAGCTGGGACTACTGGTGTATGCCACCATGCCCG TCAAGCGATTCTCCTGTTTGAGCCTCCTGAGTGGCTGGGACTACTGGTGTATGCCACCATGCCCG T C ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1237588136 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24593253 37083 RMVar_ID_37083 Human_SNP_ID_34729373 A-to-I Human chr1 - 155556786 155556786 155556786 CTTCAGACTCCCAAATTGCTGGAATTATAGGCATGAGCTACCACACCTGGGCAATTTTGTTCATT CTTCAGACTCCCAAATTGCTGGAATTATAGGCGTGAGCTACCACACCTGGGCAATTTTGTTCATT T C ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1236079850 Functional Loss SNV dbSNP153 33..33 33 - - - 37084 RMVar_ID_37084 Human_SNP_ID_34729374 A-to-I Human chr1 - 155556786 155556786 155556786 CTTCAGACTCCCAAATTGCTGGAATTATAGGCATGAGCTACCACACCTGGGCAATTTTGTTCATT CTTCAGACTCCCAAATTGCTGGAATTATAGGCCTGAGCTACCACACCTGGGCAATTTTGTTCATT T G ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1236079850 Functional Loss SNV dbSNP153 33..33 33 - - - 37085 RMVar_ID_37085 Human_SNP_ID_34729789 A-to-I Human chr1 - 155558440 155558440 155558440 TGAGAGAGAGTTTCGCTCTTGTTGTCCAGCCTAGAGTGCAACAGCGCGATCTCAGCTCGCTGCAA TGAGAGAGAGTTTCGCTCTTGTTGTCCAGCCTGGAGTGCAACAGCGCGATCTCAGCTCGCTGCAA T C ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs898616571 Functional Loss SNV dbSNP153 33..33 33 - - - 37086 RMVar_ID_37086 Human_SNP_ID_34732320 A-to-I Human chr1 + 155566377 155566377 155566377 TTTCAGGCTGGGCGCAGTGGCTCATGCCTATAAATCCCAACACTTTGGGCGACTGAGGCAGGAGG TTTCAGGCTGGGCGCAGTGGCTCATGCCTATACATCCCAACACTTTGGGCGACTGAGGCAGGAGG A C ASH1L-AS1,ASH1L-AS1:2,ASH1L-AS1:3 RNACentral:URS0000D5A569,RNACentral:URS0000D57E5C,RNACentral:URS0000D5E18C lincRNA,lincRNA,lincRNA exon,intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1362831778 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10598850 37087 RMVar_ID_37087 Human_SNP_ID_34732334 A-to-I Human chr1 + 155566423 155566423 155566423 GGGCGACTGAGGCAGGAGGATTACTTGAGGCCAGGAGTTCAAGACCAGCCTGGTTAACATAGCAA GGGCGACTGAGGCAGGAGGATTACTTGAGGCCTGGAGTTCAAGACCAGCCTGGTTAACATAGCAA A T ASH1L-AS1,ASH1L-AS1:2,ASH1L-AS1:3 RNACentral:URS0000D5A569,RNACentral:URS0000D57E5C,RNACentral:URS0000D5E18C lincRNA,lincRNA,lincRNA exon,intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs993404590 Functional Loss SNV dbSNP153 33..33 33 - - - 37088 RMVar_ID_37088 Human_SNP_ID_34734171 A-to-I Human chr1 + 155573305 155573305 155573305 TACCCAAGTGGGCCAGACAGTGGCTCACATCTATAATCCCAGCACTTTGAGAGGCCAAGGCAGGT TACCCAAGTGGGCCAGACAGTGGCTCACATCTGTAATCCCAGCACTTTGAGAGGCCAAGGCAGGT A G ASH1L-AS1 RNACentral:URS0000D5A569 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs943354561 Functional Loss SNV dbSNP153 33..33 33 - - - 37089 RMVar_ID_37089 Human_SNP_ID_34746792 A-to-I Human chr1 + 155620193 155620193 155620193 CTTTTTATTTTTTGTAGAGGCGGGGTTTTGCTATGTTGTCCAGGCTGGCCTTGAAACCCTGAGCT CTTTTTATTTTTTGTAGAGGCGGGGTTTTGCTGTGTTGTCCAGGCTGGCCTTGAAACCCTGAGCT A G ASH1L-AS1 RNACentral:URS0000D5A569 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs530862545 Functional Loss SNV dbSNP153 33..33 33 - - - 37090 RMVar_ID_37090 Human_SNP_ID_34747194 A-to-I Human chr1 + 155621579 155621579 155621579 ACAATCTCGGCTCACTGCACCCTCTGCCTTCCAGGCTCAATCTATTCTCCTGCCTCAGCCTCTTG ACAATCTCGGCTCACTGCACCCTCTGCCTTCCGGGCTCAATCTATTCTCCTGCCTCAGCCTCTTG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs925735958 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10599368 37091 RMVar_ID_37091 Human_SNP_ID_34757412 A-to-I Human chr1 - 155661784 155661784 155661784 GGGTGTGGTGGCGGGCACCTGTAGTCCCAGCTACTCCGGAGGCTGAGGCAGGAGAATGGCGTGAA GGGTGTGGTGGCGGGCACCTGTAGTCCCAGCTGCTCCGGAGGCTGAGGCAGGAGAATGGCGTGAA T C YY1AP1 Ensembl:ENSG00000163374 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1212671107 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78938,RMVar_hsa_circ_103917,RMVar_hsa_circ_265400,RMVar_hsa_circ_136651,RMVar_hsa_circ_26391,RMVar_hsa_circ_68465,RMVar_hsa_circ_136652 37092 RMVar_ID_37092 Human_SNP_ID_34757426 A-to-I Human chr1 - 155661837 155661837 155661837 CCTGGCTAACACAGTGAAACCCTGTCTCTACTAAAAATACAAAAAAATCAGCCGGGTGTGGTGGC CCTGGCTAACACAGTGAAACCCTGTCTCTACTGAAAATACAAAAAAATCAGCCGGGTGTGGTGGC T C YY1AP1 Ensembl:ENSG00000163374 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs928313307 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78938,RMVar_hsa_circ_103917,RMVar_hsa_circ_265400,RMVar_hsa_circ_136651,RMVar_hsa_circ_26391,RMVar_hsa_circ_68465,RMVar_hsa_circ_136652 37093 RMVar_ID_37093 Human_SNP_ID_34757427 A-to-I Human chr1 - 155661840 155661840 155661840 CATCCTGGCTAACACAGTGAAACCCTGTCTCTACTAAAAATACAAAAAAATCAGCCGGGTGTGGT CATCCTGGCTAACACAGTGAAACCCTGTCTCTGCTAAAAATACAAAAAAATCAGCCGGGTGTGGT T C YY1AP1 Ensembl:ENSG00000163374 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1435264405 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78938,RMVar_hsa_circ_103917,RMVar_hsa_circ_265400,RMVar_hsa_circ_136651,RMVar_hsa_circ_26391,RMVar_hsa_circ_68465,RMVar_hsa_circ_136652 37094 RMVar_ID_37094 Human_SNP_ID_34757432 A-to-I Human chr1 - 155661857 155661857 155661857 GGTCAGGAGATCGAGACCATCCTGGCTAACACAGTGAAACCCTGTCTCTACTAAAAATACAAAAA GGTCAGGAGATCGAGACCATCCTGGCTAACACGGTGAAACCCTGTCTCTACTAAAAATACAAAAA T C YY1AP1 Ensembl:ENSG00000163374 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1324110273 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78938,RMVar_hsa_circ_103917,RMVar_hsa_circ_265400,RMVar_hsa_circ_136651,RMVar_hsa_circ_26391,RMVar_hsa_circ_68465,RMVar_hsa_circ_136652 37095 RMVar_ID_37095 Human_SNP_ID_34757559 A-to-I Human chr1 - 155662382 155662382 155662382 GGTTCAAGCGATTCTTTTGCCCCAGCCTCCCAAGTAACTGGGATTACAGGCACCCACCACCACAC GGTTCAAGCGATTCTTTTGCCCCAGCCTCCCAGGTAACTGGGATTACAGGCACCCACCACCACAC T C YY1AP1 Ensembl:ENSG00000163374 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893087852 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78938,RMVar_hsa_circ_103917,RMVar_hsa_circ_265400,RMVar_hsa_circ_136651,RMVar_hsa_circ_26391,RMVar_hsa_circ_68465,RMVar_hsa_circ_136652 37096 RMVar_ID_37096 Human_SNP_ID_34757677 A-to-I Human chr1 - 155662888 155662888 155662888 GTGATTCTCCTGCCTCAGCCTGCCAAGTAGCTAGGATCACAGGCGTGCACCACCACACCCAGCTA GTGATTCTCCTGCCTCAGCCTGCCAAGTAGCTGGGATCACAGGCGTGCACCACCACACCCAGCTA T C YY1AP1 Ensembl:ENSG00000163374 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1311530443 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78938,RMVar_hsa_circ_103917,RMVar_hsa_circ_265400,RMVar_hsa_circ_136651,RMVar_hsa_circ_26391,RMVar_hsa_circ_68465,RMVar_hsa_circ_136652 37097 RMVar_ID_37097 Human_SNP_ID_34758226 A-to-I Human chr1 - 155664902 155664902 155664902 AGCCGGGTGTGGTGGCGGGCGTCTGTAGTCCCAGGTACTCTGGAGGCTGAGGCAGGAGAATGGCG AGCCGGGTGTGGTGGCGGGCGTCTGTAGTCCCGGGTACTCTGGAGGCTGAGGCAGGAGAATGGCG T C YY1AP1 Ensembl:ENSG00000163374 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs897438514 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78938,RMVar_hsa_circ_103917,RMVar_hsa_circ_265400,RMVar_hsa_circ_136651,RMVar_hsa_circ_26391,RMVar_hsa_circ_68465,RMVar_hsa_circ_136652 37098 RMVar_ID_37098 Human_SNP_ID_34758410 A-to-I Human chr1 - 155665512 155665512 155665512 TCACTGCAACGTCCGCCTCCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGA TCACTGCAACGTCCGCCTCCCGGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGA T C YY1AP1 Ensembl:ENSG00000163374 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1264777506 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78938,RMVar_hsa_circ_103917,RMVar_hsa_circ_265400,RMVar_hsa_circ_136651,RMVar_hsa_circ_26391,RMVar_hsa_circ_68465,RMVar_hsa_circ_136652 37099 RMVar_ID_37099 Human_SNP_ID_34758474 A-to-I Human chr1 - 155665683 155665683 155665683 GTCTTGAACTCCTGACCTCAGGGGATCCACCCACCTCAGCCTCCCAGAGTGCGGGGATTACAGGC GTCTTGAACTCCTGACCTCAGGGGATCCACCCGCCTCAGCCTCCCAGAGTGCGGGGATTACAGGC T C YY1AP1 Ensembl:ENSG00000163374 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1401019467 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78938,RMVar_hsa_circ_103917,RMVar_hsa_circ_265400,RMVar_hsa_circ_136651,RMVar_hsa_circ_26391,RMVar_hsa_circ_68465,RMVar_hsa_circ_136652 37100 RMVar_ID_37100 Human_SNP_ID_34758667 A-to-I Human chr1 - 155666302 155666302 155666302 CCTGGCTAACATGGTGAAACCCCAGCTCTACTAAAAATACAAAAAACTGGCTGGGCGTGGTGGCG CCTGGCTAACATGGTGAAACCCCAGCTCTACTGAAAATACAAAAAACTGGCTGGGCGTGGTGGCG T C YY1AP1 Ensembl:ENSG00000163374 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1280103073 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78938,RMVar_hsa_circ_103917,RMVar_hsa_circ_265400,RMVar_hsa_circ_136651,RMVar_hsa_circ_26391,RMVar_hsa_circ_68465,RMVar_hsa_circ_136652 37101 RMVar_ID_37101 Human_SNP_ID_34758801 A-to-I Human chr1 - 155666817 155666817 155666817 TTTTATATTTTTAGTAGAAACATAATTTCACCATGTTGGTCAGTCTGATCTTGAACTCCTGATCT TTTTATATTTTTAGTAGAAACATAATTTCACCGTGTTGGTCAGTCTGATCTTGAACTCCTGATCT T C YY1AP1 Ensembl:ENSG00000163374 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1425881935 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10599638 RMVar_hsa_circ_78938,RMVar_hsa_circ_103917,RMVar_hsa_circ_265400,RMVar_hsa_circ_136651,RMVar_hsa_circ_26391,RMVar_hsa_circ_68465,RMVar_hsa_circ_136652 37102 RMVar_ID_37102 Human_SNP_ID_34758992 A-to-I Human chr1 - 155667641 155667641 155667641 ATTTTTGTATTTAGTAGAGTCGGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCT ATTTTTGTATTTAGTAGAGTCGGGGTTTCACCGTGTTGGCCAGGCTGGTCTCGAACTCCTGACCT T C YY1AP1 Ensembl:ENSG00000163374 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1189857022 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10599682 RMVar_hsa_circ_78938,RMVar_hsa_circ_103917,RMVar_hsa_circ_265400,RMVar_hsa_circ_136651,RMVar_hsa_circ_26391,RMVar_hsa_circ_68465,RMVar_hsa_circ_136652 37103 RMVar_ID_37103 Human_SNP_ID_34759879 A-to-I Human chr1 - 155670803 155670803 155670803 AGGCGTGGTGGCAGGCGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATGGCCTGAA AGGCGTGGTGGCAGGCGCCTGTAGTCCCAGCTGCTCAGGAGGCTGAGGCAGGAGAATGGCCTGAA T C YY1AP1 Ensembl:ENSG00000163374 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1203573801 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6989,RMVar_hsa_circ_78938,RMVar_hsa_circ_26391,RMVar_hsa_circ_68465,RMVar_hsa_circ_136652,RMVar_hsa_circ_297077,RMVar_hsa_circ_324879,RMVar_hsa_circ_40466,RMVar_hsa_circ_136660,RMVar_hsa_circ_291675,RMVar_hsa_circ_136655,RMVar_hsa_circ_136656,RMVar_hsa_circ_136654,RMVar_hsa_circ_339529,RMVar_hsa_circ_340434,RMVar_hsa_circ_323095,RMVar_hsa_circ_273574,RMVar_hsa_circ_289095,RMVar_hsa_circ_136658,RMVar_hsa_circ_136659 37104 RMVar_ID_37104 Human_SNP_ID_34759881 A-to-I Human chr1 - 155670807 155670807 155670807 AGCCAGGCGTGGTGGCAGGCGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATGGCC AGCCAGGCGTGGTGGCAGGCGCCTGTAGTCCCGGCTACTCAGGAGGCTGAGGCAGGAGAATGGCC T C YY1AP1 Ensembl:ENSG00000163374 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1311951009 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6989,RMVar_hsa_circ_78938,RMVar_hsa_circ_26391,RMVar_hsa_circ_68465,RMVar_hsa_circ_136652,RMVar_hsa_circ_297077,RMVar_hsa_circ_324879,RMVar_hsa_circ_40466,RMVar_hsa_circ_136660,RMVar_hsa_circ_291675,RMVar_hsa_circ_136655,RMVar_hsa_circ_136656,RMVar_hsa_circ_136654,RMVar_hsa_circ_339529,RMVar_hsa_circ_340434,RMVar_hsa_circ_323095,RMVar_hsa_circ_273574,RMVar_hsa_circ_289095,RMVar_hsa_circ_136658,RMVar_hsa_circ_136659 37105 RMVar_ID_37105 Human_SNP_ID_34759901 A-to-I Human chr1 - 155670869 155670869 155670869 CAGGAGATCAAGACCATCCTGTCTACAGTGAAACCCCGTCTCTACTAAAAATACAAAAAATCAGC CAGGAGATCAAGACCATCCTGTCTACAGTGAACCCCCGTCTCTACTAAAAATACAAAAAATCAGC T G YY1AP1 Ensembl:ENSG00000163374 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs12727901 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22847831 RMVar_hsa_circ_6989,RMVar_hsa_circ_78938,RMVar_hsa_circ_26391,RMVar_hsa_circ_68465,RMVar_hsa_circ_136652,RMVar_hsa_circ_297077,RMVar_hsa_circ_324879,RMVar_hsa_circ_40466,RMVar_hsa_circ_136660,RMVar_hsa_circ_291675,RMVar_hsa_circ_136655,RMVar_hsa_circ_136656,RMVar_hsa_circ_136654,RMVar_hsa_circ_339529,RMVar_hsa_circ_340434,RMVar_hsa_circ_323095,RMVar_hsa_circ_273574,RMVar_hsa_circ_289095,RMVar_hsa_circ_136658,RMVar_hsa_circ_136659 37106 RMVar_ID_37106 Human_SNP_ID_34759924 A-to-I Human chr1 - 155670937 155670937 155670937 GGCCGGGCGCCGTGGCTTACGCCTGTAATCCAACACTTTAGGAGGCCGAGGCTGTCGGATGACAA GGCCGGGCGCCGTGGCTTACGCCTGTAATCCAGCACTTTAGGAGGCCGAGGCTGTCGGATGACAA T C YY1AP1 Ensembl:ENSG00000163374 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs12728041 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6989,RMVar_hsa_circ_78938,RMVar_hsa_circ_26391,RMVar_hsa_circ_68465,RMVar_hsa_circ_136652,RMVar_hsa_circ_297077,RMVar_hsa_circ_324879,RMVar_hsa_circ_40466,RMVar_hsa_circ_136660,RMVar_hsa_circ_291675,RMVar_hsa_circ_136655,RMVar_hsa_circ_136656,RMVar_hsa_circ_136654,RMVar_hsa_circ_339529,RMVar_hsa_circ_340434,RMVar_hsa_circ_323095,RMVar_hsa_circ_273574,RMVar_hsa_circ_289095,RMVar_hsa_circ_136658,RMVar_hsa_circ_136659 37107 RMVar_ID_37107 Human_SNP_ID_34759925 A-to-I Human chr1 - 155670937 155670937 155670937 GGCCGGGCGCCGTGGCTTACGCCTGTAATCCAACACTTTAGGAGGCCGAGGCTGTCGGATGACAA GGCCGGGCGCCGTGGCTTACGCCTGTAATCCACCACTTTAGGAGGCCGAGGCTGTCGGATGACAA T G YY1AP1 Ensembl:ENSG00000163374 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs12728041 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6989,RMVar_hsa_circ_78938,RMVar_hsa_circ_26391,RMVar_hsa_circ_68465,RMVar_hsa_circ_136652,RMVar_hsa_circ_297077,RMVar_hsa_circ_324879,RMVar_hsa_circ_40466,RMVar_hsa_circ_136660,RMVar_hsa_circ_291675,RMVar_hsa_circ_136655,RMVar_hsa_circ_136656,RMVar_hsa_circ_136654,RMVar_hsa_circ_339529,RMVar_hsa_circ_340434,RMVar_hsa_circ_323095,RMVar_hsa_circ_273574,RMVar_hsa_circ_289095,RMVar_hsa_circ_136658,RMVar_hsa_circ_136659 37108 RMVar_ID_37108 Human_SNP_ID_34760025 A-to-I Human chr1 - 155671344 155671344 155671344 TCACTGCAACCTCCGCCTCCCAGGTTCAAACAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGAA TCACTGCAACCTCCGCCTCCCAGGTTCAAACAGTTCTCCTGCCTCAGCCTCCCAAGTAGCTGGAA T C YY1AP1 Ensembl:ENSG00000163374 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1051173535 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6989,RMVar_hsa_circ_78938,RMVar_hsa_circ_26391,RMVar_hsa_circ_68465,RMVar_hsa_circ_136652,RMVar_hsa_circ_297077,RMVar_hsa_circ_324879,RMVar_hsa_circ_40466,RMVar_hsa_circ_136660,RMVar_hsa_circ_291675,RMVar_hsa_circ_136655,RMVar_hsa_circ_136656,RMVar_hsa_circ_136654,RMVar_hsa_circ_339529,RMVar_hsa_circ_340434,RMVar_hsa_circ_323095,RMVar_hsa_circ_273574,RMVar_hsa_circ_289095,RMVar_hsa_circ_136658,RMVar_hsa_circ_136659 37109 RMVar_ID_37109 Human_SNP_ID_34760026 A-to-I Human chr1 - 155671348 155671348 155671348 CGGCTCACTGCAACCTCCGCCTCCCAGGTTCAAACAATTCTCCTGCCTCAGCCTCCCAAGTAGCT CGGCTCACTGCAACCTCCGCCTCCCAGGTTCATACAATTCTCCTGCCTCAGCCTCCCAAGTAGCT T A YY1AP1 Ensembl:ENSG00000163374 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1201167547 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6989,RMVar_hsa_circ_78938,RMVar_hsa_circ_26391,RMVar_hsa_circ_68465,RMVar_hsa_circ_136652,RMVar_hsa_circ_297077,RMVar_hsa_circ_324879,RMVar_hsa_circ_40466,RMVar_hsa_circ_136660,RMVar_hsa_circ_291675,RMVar_hsa_circ_136655,RMVar_hsa_circ_136656,RMVar_hsa_circ_136654,RMVar_hsa_circ_339529,RMVar_hsa_circ_340434,RMVar_hsa_circ_323095,RMVar_hsa_circ_273574,RMVar_hsa_circ_289095,RMVar_hsa_circ_136658,RMVar_hsa_circ_136659 37110 RMVar_ID_37110 Human_SNP_ID_34760027 A-to-I Human chr1 - 155671348 155671348 155671348 CGGCTCACTGCAACCTCCGCCTCCCAGGTTCAAACAATTCTCCTGCCTCAGCCTCCCAAGTAGCT CGGCTCACTGCAACCTCCGCCTCCCAGGTTCAGACAATTCTCCTGCCTCAGCCTCCCAAGTAGCT T C YY1AP1 Ensembl:ENSG00000163374 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1201167547 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6989,RMVar_hsa_circ_78938,RMVar_hsa_circ_26391,RMVar_hsa_circ_68465,RMVar_hsa_circ_136652,RMVar_hsa_circ_297077,RMVar_hsa_circ_324879,RMVar_hsa_circ_40466,RMVar_hsa_circ_136660,RMVar_hsa_circ_291675,RMVar_hsa_circ_136655,RMVar_hsa_circ_136656,RMVar_hsa_circ_136654,RMVar_hsa_circ_339529,RMVar_hsa_circ_340434,RMVar_hsa_circ_323095,RMVar_hsa_circ_273574,RMVar_hsa_circ_289095,RMVar_hsa_circ_136658,RMVar_hsa_circ_136659 37111 RMVar_ID_37111 Human_SNP_ID_34760037 A-to-I Human chr1 - 155671374 155671374 155671374 TAGGCTGGAGTGCAGTGGGGTGATCTCGGCTCACTGCAACCTCCGCCTCCCAGGTTCAAACAATT TAGGCTGGAGTGCAGTGGGGTGATCTCGGCTCGCTGCAACCTCCGCCTCCCAGGTTCAAACAATT T C YY1AP1 Ensembl:ENSG00000163374 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs891360329 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6989,RMVar_hsa_circ_78938,RMVar_hsa_circ_26391,RMVar_hsa_circ_68465,RMVar_hsa_circ_136652,RMVar_hsa_circ_297077,RMVar_hsa_circ_324879,RMVar_hsa_circ_40466,RMVar_hsa_circ_136660,RMVar_hsa_circ_291675,RMVar_hsa_circ_136655,RMVar_hsa_circ_136656,RMVar_hsa_circ_136654,RMVar_hsa_circ_339529,RMVar_hsa_circ_340434,RMVar_hsa_circ_323095,RMVar_hsa_circ_273574,RMVar_hsa_circ_289095,RMVar_hsa_circ_136658,RMVar_hsa_circ_136659 37112 RMVar_ID_37112 Human_SNP_ID_34760478 A-to-I Human chr1 - 155673116 155673116 155673116 AGCTTCTCAGGAGGCAGTGGGAGGATGGCTTGAGCCTGGGAGGGGGAGTTTGCAGTGAGCTGAGA AGCTTCTCAGGAGGCAGTGGGAGGATGGCTTGGGCCTGGGAGGGGGAGTTTGCAGTGAGCTGAGA T C YY1AP1 Ensembl:ENSG00000163374 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1288775532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22560357 RMVar_hsa_circ_78938,RMVar_hsa_circ_26391,RMVar_hsa_circ_68465,RMVar_hsa_circ_136652,RMVar_hsa_circ_297077,RMVar_hsa_circ_324879,RMVar_hsa_circ_40466,RMVar_hsa_circ_32311,RMVar_hsa_circ_136660,RMVar_hsa_circ_291675,RMVar_hsa_circ_136655,RMVar_hsa_circ_136656,RMVar_hsa_circ_136654,RMVar_hsa_circ_340434,RMVar_hsa_circ_273574,RMVar_hsa_circ_289095,RMVar_hsa_circ_136658,RMVar_hsa_circ_136659,RMVar_hsa_circ_333378,RMVar_hsa_circ_301022,RMVar_hsa_circ_136661 37113 RMVar_ID_37113 Human_SNP_ID_34760487 A-to-I Human chr1 - 155673156 155673156 155673156 CAAAAATCAGCTAGGTTTGGAGGTGTATGCCTATAGTCCCAGCTTCTCAGGAGGCAGTGGGAGGA CAAAAATCAGCTAGGTTTGGAGGTGTATGCCTGTAGTCCCAGCTTCTCAGGAGGCAGTGGGAGGA T C YY1AP1 Ensembl:ENSG00000163374 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1215896874 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78938,RMVar_hsa_circ_26391,RMVar_hsa_circ_68465,RMVar_hsa_circ_136652,RMVar_hsa_circ_297077,RMVar_hsa_circ_324879,RMVar_hsa_circ_40466,RMVar_hsa_circ_32311,RMVar_hsa_circ_136660,RMVar_hsa_circ_291675,RMVar_hsa_circ_136655,RMVar_hsa_circ_136656,RMVar_hsa_circ_136654,RMVar_hsa_circ_340434,RMVar_hsa_circ_273574,RMVar_hsa_circ_289095,RMVar_hsa_circ_136658,RMVar_hsa_circ_136659,RMVar_hsa_circ_333378,RMVar_hsa_circ_301022,RMVar_hsa_circ_136661 37114 RMVar_ID_37114 Human_SNP_ID_34760628 A-to-I Human chr1 - 155673708 155673708 155673708 TCCCTACCAAAAAAATAAAAAATAAAAAAATTAGCTGGGGATGGTGCCGAGTGCCTGTAGTCCCA TCCCTACCAAAAAAATAAAAAATAAAAAAATTCGCTGGGGATGGTGCCGAGTGCCTGTAGTCCCA T G YY1AP1 Ensembl:ENSG00000163374 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1210921016 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24593412 RMVar_hsa_circ_78938,RMVar_hsa_circ_26391,RMVar_hsa_circ_68465,RMVar_hsa_circ_136652,RMVar_hsa_circ_297077,RMVar_hsa_circ_324879,RMVar_hsa_circ_40466,RMVar_hsa_circ_32311,RMVar_hsa_circ_136660,RMVar_hsa_circ_291675,RMVar_hsa_circ_136655,RMVar_hsa_circ_136656,RMVar_hsa_circ_136654,RMVar_hsa_circ_340434,RMVar_hsa_circ_273574,RMVar_hsa_circ_289095,RMVar_hsa_circ_136658,RMVar_hsa_circ_136659,RMVar_hsa_circ_333378,RMVar_hsa_circ_301022,RMVar_hsa_circ_136661 37115 RMVar_ID_37115 Human_SNP_ID_34761306 A-to-I Human chr1 - 155676110 155676110 155676110 TCACGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGTGACTACAGGGACTCGCCACCACACCCA TCACGCCATTCTCCTGCCTCAGCCTCCCGAGTCGCTGTGACTACAGGGACTCGCCACCACACCCA T G YY1AP1 Ensembl:ENSG00000163374 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1318874865 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136663,RMVar_hsa_circ_78938,RMVar_hsa_circ_26391,RMVar_hsa_circ_68465,RMVar_hsa_circ_136652,RMVar_hsa_circ_297077,RMVar_hsa_circ_40466,RMVar_hsa_circ_136660,RMVar_hsa_circ_291675,RMVar_hsa_circ_136655,RMVar_hsa_circ_136656,RMVar_hsa_circ_340434,RMVar_hsa_circ_289095,RMVar_hsa_circ_136659,RMVar_hsa_circ_333378,RMVar_hsa_circ_301022,RMVar_hsa_circ_270419,RMVar_hsa_circ_136661,RMVar_hsa_circ_323451,RMVar_hsa_circ_286479,RMVar_hsa_circ_109088,RMVar_hsa_circ_265997,RMVar_hsa_circ_136664,RMVar_hsa_circ_136662 37116 RMVar_ID_37116 Human_SNP_ID_34762289 A-to-I Human chr1 - 155679967 155679967 155679967 CTTGCCATGTTCTGGAACTCATAGGCTCAAGTAATCTTCCTGCCTCAACCTCCCAAAGTGCTGGA CTTGCCATGTTCTGGAACTCATAGGCTCAAGTGATCTTCCTGCCTCAACCTCCCAAAGTGCTGGA T C YY1AP1 Ensembl:ENSG00000163374 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1261693024 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10600040,Human_RBP_ID_24593461 Human_Splice_Rec_139412,Human_Splice_Rec_139413,Human_Splice_Rec_139650,Human_Splice_Rec_139651 RMVar_hsa_circ_136663,RMVar_hsa_circ_78938,RMVar_hsa_circ_68465,RMVar_hsa_circ_136652,RMVar_hsa_circ_297077,RMVar_hsa_circ_136660,RMVar_hsa_circ_291675,RMVar_hsa_circ_136656,RMVar_hsa_circ_340434,RMVar_hsa_circ_286479,RMVar_hsa_circ_109088,RMVar_hsa_circ_68437,RMVar_hsa_circ_136667,RMVar_hsa_circ_136662,RMVar_hsa_circ_275688,RMVar_hsa_circ_136668 37117 RMVar_ID_37117 Human_SNP_ID_34762665 A-to-I Human chr1 - 155681529 155681529 155681529 GCTGGAATGCAGTGGGACGGTCTCAGCTCACTACAGCCTCTGCTTCTTGGACTCAAAGAGATTCT GCTGGAATGCAGTGGGACGGTCTCAGCTCACTGCAGCCTCTGCTTCTTGGACTCAAAGAGATTCT T C YY1AP1 Ensembl:ENSG00000163374 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1342464210 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10600108 RMVar_hsa_circ_78938,RMVar_hsa_circ_136652,RMVar_hsa_circ_109088,RMVar_hsa_circ_68437,RMVar_hsa_circ_136662,RMVar_hsa_circ_136668 37118 RMVar_ID_37118 Human_SNP_ID_34762671 A-to-I Human chr1 - 155681555 155681555 155681555 AGACAGTGTCTTGCTCTGTCGTTCAGGCTGGAATGCAGTGGGACGGTCTCAGCTCACTACAGCCT AGACAGTGTCTTGCTCTGTCGTTCAGGCTGGAGTGCAGTGGGACGGTCTCAGCTCACTACAGCCT T C YY1AP1 Ensembl:ENSG00000163374 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs558474741 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5695245,Human_RBP_ID_10600111 RMVar_hsa_circ_78938,RMVar_hsa_circ_136652,RMVar_hsa_circ_109088,RMVar_hsa_circ_68437,RMVar_hsa_circ_136662,RMVar_hsa_circ_136668 37119 RMVar_ID_37119 Human_SNP_ID_34762672 A-to-I Human chr1 - 155681555 155681555 155681555 AGACAGTGTCTTGCTCTGTCGTTCAGGCTGGAATGCAGTGGGACGGTCTCAGCTCACTACAGCCT AGACAGTGTCTTGCTCTGTCGTTCAGGCTGGACTGCAGTGGGACGGTCTCAGCTCACTACAGCCT T G YY1AP1 Ensembl:ENSG00000163374 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs558474741 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5695245,Human_RBP_ID_10600111 RMVar_hsa_circ_78938,RMVar_hsa_circ_136652,RMVar_hsa_circ_109088,RMVar_hsa_circ_68437,RMVar_hsa_circ_136662,RMVar_hsa_circ_136668 37120 RMVar_ID_37120 Human_SNP_ID_34762941 A-to-I Human chr1 - 155682549 155682549 155682549 GGAGACCAACCTGGCCAACATGATGAAACCCCATCTCTACTAAAAATACAAAAAATTATCCAGGT GGAGACCAACCTGGCCAACATGATGAAACCCCGTCTCTACTAAAAATACAAAAAATTATCCAGGT T C YY1AP1 Ensembl:ENSG00000163374 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1558316548 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78938,RMVar_hsa_circ_136652,RMVar_hsa_circ_109088,RMVar_hsa_circ_68437,RMVar_hsa_circ_136662,RMVar_hsa_circ_136668 37121 RMVar_ID_37121 Human_SNP_ID_34763150 A-to-I Human chr1 - 155683414 155683414 155683414 ATACTCCTGACCTCAAGTGATCCACCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG ATACTCCTGACCTCAAGTGATCCACCTGCCTCTGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG T A YY1AP1 Ensembl:ENSG00000163374 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1471645256 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78938,RMVar_hsa_circ_136652,RMVar_hsa_circ_109088,RMVar_hsa_circ_68437,RMVar_hsa_circ_136662,RMVar_hsa_circ_136668 37122 RMVar_ID_37122 Human_SNP_ID_34763151 A-to-I Human chr1 - 155683414 155683414 155683414 ATACTCCTGACCTCAAGTGATCCACCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG ATACTCCTGACCTCAAGTGATCCACCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG T C YY1AP1 Ensembl:ENSG00000163374 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1471645256 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78938,RMVar_hsa_circ_136652,RMVar_hsa_circ_109088,RMVar_hsa_circ_68437,RMVar_hsa_circ_136662,RMVar_hsa_circ_136668 37123 RMVar_ID_37123 Human_SNP_ID_34763156 A-to-I Human chr1 - 155683431 155683431 155683431 GTAGCCAAGCTGTTCTCATACTCCTGACCTCAAGTGATCCACCTGCCTCAGCCTCCCAAAGTGCT GTAGCCAAGCTGTTCTCATACTCCTGACCTCAGGTGATCCACCTGCCTCAGCCTCCCAAAGTGCT T C YY1AP1 Ensembl:ENSG00000163374 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1013498466 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78938,RMVar_hsa_circ_136652,RMVar_hsa_circ_109088,RMVar_hsa_circ_68437,RMVar_hsa_circ_136662,RMVar_hsa_circ_136668 37124 RMVar_ID_37124 Human_SNP_ID_34763165 A-to-I Human chr1 - 155683490 155683490 155683490 CACTACACCTGGCTAATTTTTGTATTGTTAGTAGAGACAGGGTTTCACCATGTTAGCCAGTAGCC CACTACACCTGGCTAATTTTTGTATTGTTAGTTGAGACAGGGTTTCACCATGTTAGCCAGTAGCC T A YY1AP1 Ensembl:ENSG00000163374 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs905109375 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78938,RMVar_hsa_circ_136652,RMVar_hsa_circ_109088,RMVar_hsa_circ_68437,RMVar_hsa_circ_136662,RMVar_hsa_circ_136668 37125 RMVar_ID_37125 Human_SNP_ID_34763166 A-to-I Human chr1 - 155683493 155683493 155683493 CACCACTACACCTGGCTAATTTTTGTATTGTTAGTAGAGACAGGGTTTCACCATGTTAGCCAGTA CACCACTACACCTGGCTAATTTTTGTATTGTTGGTAGAGACAGGGTTTCACCATGTTAGCCAGTA T C YY1AP1 Ensembl:ENSG00000163374 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559336722 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78938,RMVar_hsa_circ_136652,RMVar_hsa_circ_109088,RMVar_hsa_circ_68437,RMVar_hsa_circ_136662,RMVar_hsa_circ_136668 37126 RMVar_ID_37126 Human_SNP_ID_34763271 A-to-I Human chr1 - 155683950 155683950 155683950 AGCCACTGCACCTGGCCCAGGTCTTGCTATGTAGATCAATCTGGTCTTGAACTCCTGGCCTCAAG AGCCACTGCACCTGGCCCAGGTCTTGCTATGTGGATCAATCTGGTCTTGAACTCCTGGCCTCAAG T C YY1AP1 Ensembl:ENSG00000163374 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs575640546 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1149863,Human_RBP_ID_10600185,Human_RBP_ID_24593507 RMVar_hsa_circ_78938,RMVar_hsa_circ_136652,RMVar_hsa_circ_109088,RMVar_hsa_circ_68437,RMVar_hsa_circ_136662,RMVar_hsa_circ_136668 37127 RMVar_ID_37127 Human_SNP_ID_34763273 A-to-I Human chr1 - 155683954 155683954 155683954 AGTGAGCCACTGCACCTGGCCCAGGTCTTGCTATGTAGATCAATCTGGTCTTGAACTCCTGGCCT AGTGAGCCACTGCACCTGGCCCAGGTCTTGCTGTGTAGATCAATCTGGTCTTGAACTCCTGGCCT T C YY1AP1 Ensembl:ENSG00000163374 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1377554047 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1149863,Human_RBP_ID_10600185,Human_RBP_ID_24593507 RMVar_hsa_circ_78938,RMVar_hsa_circ_136652,RMVar_hsa_circ_109088,RMVar_hsa_circ_68437,RMVar_hsa_circ_136662,RMVar_hsa_circ_136668 37128 RMVar_ID_37128 Human_SNP_ID_34763476 A-to-I Human chr1 - 155684636 155684636 155684636 GAACTGGGAGGGGGAAGTTGCAGTGAGCTGAAATCATGCCACTGCACTCTAGCCTCGGCATCAGA GAACTGGGAGGGGGAAGTTGCAGTGAGCTGAAGTCATGCCACTGCACTCTAGCCTCGGCATCAGA T C YY1AP1 Ensembl:ENSG00000163374 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1004637221 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557340 RMVar_hsa_circ_78938,RMVar_hsa_circ_136652,RMVar_hsa_circ_109088,RMVar_hsa_circ_68437,RMVar_hsa_circ_136662,RMVar_hsa_circ_136668 37129 RMVar_ID_37129 Human_SNP_ID_34763477 A-to-I Human chr1 - 155684653 155684653 155684653 TGAACCAAGAATTGCTTGAACTGGGAGGGGGAAGTTGCAGTGAGCTGAAATCATGCCACTGCACT TGAACCAAGAATTGCTTGAACTGGGAGGGGGAGGTTGCAGTGAGCTGAAATCATGCCACTGCACT T C YY1AP1 Ensembl:ENSG00000163374 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs983364245 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8286801,Human_RBP_ID_10600220,Human_RBP_ID_17557340 RMVar_hsa_circ_78938,RMVar_hsa_circ_136652,RMVar_hsa_circ_109088,RMVar_hsa_circ_68437,RMVar_hsa_circ_136662,RMVar_hsa_circ_136668 37130 RMVar_ID_37130 Human_SNP_ID_34763492 A-to-I Human chr1 - 155684714 155684714 155684714 GCATGTGTTGGAGTGCACCTGTAGTCCCAGCTACTCGGGAAGCTGAGGCACGAGAATTGCTTGAA GCATGTGTTGGAGTGCACCTGTAGTCCCAGCTGCTCGGGAAGCTGAGGCACGAGAATTGCTTGAA T C YY1AP1 Ensembl:ENSG00000163374 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1039300453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10600222 RMVar_hsa_circ_78938,RMVar_hsa_circ_136652,RMVar_hsa_circ_109088,RMVar_hsa_circ_68437,RMVar_hsa_circ_136662,RMVar_hsa_circ_136668 37131 RMVar_ID_37131 Human_SNP_ID_34763531 A-to-I Human chr1 - 155684867 155684867 155684867 AAGAACAAGAAATTGGTCAGGTGGGGTGGCTCACGCCTGTAATCCTAGCACTTTGGGAGGACGAG AAGAACAAGAAATTGGTCAGGTGGGGTGGCTCCCGCCTGTAATCCTAGCACTTTGGGAGGACGAG T G YY1AP1 Ensembl:ENSG00000163374 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1451207093 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22564192 RMVar_hsa_circ_78938,RMVar_hsa_circ_136652,RMVar_hsa_circ_109088,RMVar_hsa_circ_68437,RMVar_hsa_circ_136662,RMVar_hsa_circ_136668 37132 RMVar_ID_37132 Human_SNP_ID_34765035 A-to-I Human chr1 + 155689715 155689715 155689715 GCAGGTGGATGACAAGGTGAAGAGATCGAGACAATCCTGGCCAACATGGTGAAACCCCGTCTCTA GCAGGTGGATGACAAGGTGAAGAGATCGAGACCATCCTGGCCAACATGGTGAAACCCCGTCTCTA A C DAP3 Ensembl:ENSG00000132676 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1470004565 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9178,RMVar_hsa_circ_337353 37133 RMVar_ID_37133 Human_SNP_ID_34768946 A-to-I Human chr1 + 155703811 155703811 155703811 CACCCACGTTGGCATCCCAGAGTGCTGGGATTACAGGTGTGAGCCACTGCGCCTGACCTAGACTT CACCCACGTTGGCATCCCAGAGTGCTGGGATTGCAGGTGTGAGCCACTGCGCCTGACCTAGACTT A G DAP3 Ensembl:ENSG00000132676 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs536575885 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9178,RMVar_hsa_circ_337353 37134 RMVar_ID_37134 Human_SNP_ID_34769002 A-to-I Human chr1 + 155704026 155704026 155704026 AAATTAGCCACCAGGTGGTTGCACATGCCTGTAGTCCCAGTTACTTAGGAGGCTGAGAAAGGAGG AAATTAGCCACCAGGTGGTTGCACATGCCTGTTGTCCCAGTTACTTAGGAGGCTGAGAAAGGAGG A T DAP3 Ensembl:ENSG00000132676 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs937239045 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9178,RMVar_hsa_circ_337353 37135 RMVar_ID_37135 Human_SNP_ID_34772482 A-to-I Human chr1 + 155718496 155718496 155718496 CATGAGGTCAGGAGACTGAGACCATCCTGGCTAACACAGTGAGACCCCATCTCTACTAAAAATAC CATGAGGTCAGGAGACTGAGACCATCCTGGCTGACACAGTGAGACCCCATCTCTACTAAAAATAC A G DAP3 Ensembl:ENSG00000132676 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1319380636 Functional Loss SNV dbSNP153 33..33 33 - - - 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_136674,RMVar_hsa_circ_136675 37136 RMVar_ID_37136 Human_SNP_ID_34772744 A-to-I Human chr1 + 155719416 155719416 155719416 CACCACCATGCCTGGCTAAGTTTTGTATTTTTAGTACAGATGGGGTTTTACCATGTTGGCCAGGC CACCACCATGCCTGGCTAAGTTTTGTATTTTTCGTACAGATGGGGTTTTACCATGTTGGCCAGGC A C DAP3 Ensembl:ENSG00000132676 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1189089923 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24593639 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_136674,RMVar_hsa_circ_136675 37137 RMVar_ID_37137 Human_SNP_ID_34773496 A-to-I Human chr1 + 155722132 155722132 155722132 ATGAATAATAAGGGCATAACAGGCCGGGCGCTATGGCTCACGCCTGTAATCCCAGCTGCACTTTG ATGAATAATAAGGGCATAACAGGCCGGGCGCTGTGGCTCACGCCTGTAATCCCAGCTGCACTTTG A G DAP3 Ensembl:ENSG00000132676 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs746174292 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25131,RMVar_hsa_circ_136670,RMVar_hsa_circ_124226,RMVar_hsa_circ_301144,RMVar_hsa_circ_320226,RMVar_hsa_circ_332365,RMVar_hsa_circ_317244,RMVar_hsa_circ_136673,RMVar_hsa_circ_276721,RMVar_hsa_circ_136677,RMVar_hsa_circ_136675,RMVar_hsa_circ_271004,RMVar_hsa_circ_362272,RMVar_hsa_circ_365217,RMVar_hsa_circ_118932,RMVar_hsa_circ_136676 37138 RMVar_ID_37138 Human_SNP_ID_34774462 A-to-I Human chr1 + 155726207 155726207 155726207 GCAATCTCAGGTCACCGCAACCTCCGCCTCCCAGGCTCAAGAGATTCTCCTGCCTCAGCCTCCCA GCAATCTCAGGTCACCGCAACCTCCGCCTCCCGGGCTCAAGAGATTCTCCTGCCTCAGCCTCCCA A G DAP3 Ensembl:ENSG00000132676 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs1474558762 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_139868 RMVar_hsa_circ_136670,RMVar_hsa_circ_124226,RMVar_hsa_circ_320226,RMVar_hsa_circ_332365,RMVar_hsa_circ_317244,RMVar_hsa_circ_136679,RMVar_hsa_circ_111509,RMVar_hsa_circ_362272,RMVar_hsa_circ_365217,RMVar_hsa_circ_299789,RMVar_hsa_circ_314679,RMVar_hsa_circ_309024,RMVar_hsa_circ_59888,RMVar_hsa_circ_136681,RMVar_hsa_circ_136682,RMVar_hsa_circ_136683,RMVar_hsa_circ_136680 37139 RMVar_ID_37139 Human_SNP_ID_34774463 A-to-I Human chr1 + 155726213 155726212 155726214 TCAGGTCACCGCAACCTCCGCCTCCCAGGCTCAAGAGATTCTCCTGCCTCAGCCTCCCAAGTAGC TCAGGTCACCGCAACCTCCGCCTCCCAGGCTC__GAGATTCTCCTGCCTCAGCCTCCCAAGTAGC CAA C DAP3 Ensembl:ENSG00000132676 Protein coding intron GSE38233;GSE100210;GSE99789;GSE99789 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109 - 24183664,29129909,29796672,29796672 RNA-Seq:(High) rs1388851238 Functional Loss DEL dbSNP153 33..34 33 - - - Human_Splice_Rec_139868 RMVar_hsa_circ_136670,RMVar_hsa_circ_124226,RMVar_hsa_circ_320226,RMVar_hsa_circ_332365,RMVar_hsa_circ_317244,RMVar_hsa_circ_136679,RMVar_hsa_circ_111509,RMVar_hsa_circ_362272,RMVar_hsa_circ_365217,RMVar_hsa_circ_299789,RMVar_hsa_circ_314679,RMVar_hsa_circ_309024,RMVar_hsa_circ_59888,RMVar_hsa_circ_136681,RMVar_hsa_circ_136682,RMVar_hsa_circ_136683,RMVar_hsa_circ_136680 37140 RMVar_ID_37140 Human_SNP_ID_34774464 A-to-I Human chr1 + 155726213 155726213 155726213 TCAGGTCACCGCAACCTCCGCCTCCCAGGCTCAAGAGATTCTCCTGCCTCAGCCTCCCAAGTAGC TCAGGTCACCGCAACCTCCGCCTCCCAGGCTCGAGAGATTCTCCTGCCTCAGCCTCCCAAGTAGC A G DAP3 Ensembl:ENSG00000132676 Protein coding intron GSE38233;GSE100210;GSE99789;GSE99789 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109 - 24183664,29129909,29796672,29796672 RNA-Seq:(High) rs529694490 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_139868 RMVar_hsa_circ_136670,RMVar_hsa_circ_124226,RMVar_hsa_circ_320226,RMVar_hsa_circ_332365,RMVar_hsa_circ_317244,RMVar_hsa_circ_136679,RMVar_hsa_circ_111509,RMVar_hsa_circ_362272,RMVar_hsa_circ_365217,RMVar_hsa_circ_299789,RMVar_hsa_circ_314679,RMVar_hsa_circ_309024,RMVar_hsa_circ_59888,RMVar_hsa_circ_136681,RMVar_hsa_circ_136682,RMVar_hsa_circ_136683,RMVar_hsa_circ_136680 37141 RMVar_ID_37141 Human_SNP_ID_34774513 A-to-I Human chr1 + 155726344 155726344 155726344 GGAGTCTTGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCACGATCTCAGCTCACTGCAAGCTCCGC GGAGTCTTGCTCTGTCGCCCAGGCTGGAGTGCGGTGGCACGATCTCAGCTCACTGCAAGCTCCGC A G DAP3 Ensembl:ENSG00000132676 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1185415945 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136670,RMVar_hsa_circ_124226,RMVar_hsa_circ_320226,RMVar_hsa_circ_332365,RMVar_hsa_circ_317244,RMVar_hsa_circ_136679,RMVar_hsa_circ_111509,RMVar_hsa_circ_362272,RMVar_hsa_circ_365217,RMVar_hsa_circ_299789,RMVar_hsa_circ_314679,RMVar_hsa_circ_309024,RMVar_hsa_circ_59888,RMVar_hsa_circ_136681,RMVar_hsa_circ_136682,RMVar_hsa_circ_136683,RMVar_hsa_circ_136680 37142 RMVar_ID_37142 Human_SNP_ID_34774591 A-to-I Human chr1 + 155726658 155726658 155726658 AAAGGAAAAGCCTTTGCCAGTCACGATGGCTCAAACCTATAATCCCAGCACTTTGGGAGGCTGAG AAAGGAAAAGCCTTTGCCAGTCACGATGGCTCCAACCTATAATCCCAGCACTTTGGGAGGCTGAG A C DAP3 Ensembl:ENSG00000132676 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1441385757 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557341 RMVar_hsa_circ_136670,RMVar_hsa_circ_124226,RMVar_hsa_circ_320226,RMVar_hsa_circ_332365,RMVar_hsa_circ_317244,RMVar_hsa_circ_136679,RMVar_hsa_circ_111509,RMVar_hsa_circ_362272,RMVar_hsa_circ_365217,RMVar_hsa_circ_299789,RMVar_hsa_circ_314679,RMVar_hsa_circ_309024,RMVar_hsa_circ_59888,RMVar_hsa_circ_136681,RMVar_hsa_circ_136682,RMVar_hsa_circ_136683,RMVar_hsa_circ_136680 37143 RMVar_ID_37143 Human_SNP_ID_34774603 A-to-I Human chr1 + 155726713 155726713 155726713 GGAGGCTGAGGCTGGAATATTGCTTAGAGCCCAGGAGGAGGCTGCAGTGAGCTGTGATCGCACCA GGAGGCTGAGGCTGGAATATTGCTTAGAGCCCTGGAGGAGGCTGCAGTGAGCTGTGATCGCACCA A T DAP3 Ensembl:ENSG00000132676 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs912710685 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10601040,Human_RBP_ID_17557341,Human_RBP_ID_17727015 RMVar_hsa_circ_136670,RMVar_hsa_circ_124226,RMVar_hsa_circ_320226,RMVar_hsa_circ_332365,RMVar_hsa_circ_317244,RMVar_hsa_circ_136679,RMVar_hsa_circ_111509,RMVar_hsa_circ_362272,RMVar_hsa_circ_365217,RMVar_hsa_circ_299789,RMVar_hsa_circ_314679,RMVar_hsa_circ_309024,RMVar_hsa_circ_59888,RMVar_hsa_circ_136681,RMVar_hsa_circ_136682,RMVar_hsa_circ_136683,RMVar_hsa_circ_136680 37144 RMVar_ID_37144 Human_SNP_ID_34774607 A-to-I Human chr1 + 155726742 155726742 155726742 CCCAGGAGGAGGCTGCAGTGAGCTGTGATCGCACCACTACACTCTAGCGTGGGCAACAAAGCAAG CCCAGGAGGAGGCTGCAGTGAGCTGTGATCGCGCCACTACACTCTAGCGTGGGCAACAAAGCAAG A G DAP3 Ensembl:ENSG00000132676 Protein coding intron GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs1251632473 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136670,RMVar_hsa_circ_124226,RMVar_hsa_circ_320226,RMVar_hsa_circ_332365,RMVar_hsa_circ_317244,RMVar_hsa_circ_136679,RMVar_hsa_circ_111509,RMVar_hsa_circ_362272,RMVar_hsa_circ_365217,RMVar_hsa_circ_299789,RMVar_hsa_circ_314679,RMVar_hsa_circ_309024,RMVar_hsa_circ_59888,RMVar_hsa_circ_136681,RMVar_hsa_circ_136682,RMVar_hsa_circ_136683,RMVar_hsa_circ_136680 37145 RMVar_ID_37145 Human_SNP_ID_34774610 A-to-I Human chr1 + 155726748 155726748 155726748 AGGAGGCTGCAGTGAGCTGTGATCGCACCACTACACTCTAGCGTGGGCAACAAAGCAAGACCCTG AGGAGGCTGCAGTGAGCTGTGATCGCACCACTGCACTCTAGCGTGGGCAACAAAGCAAGACCCTG A G DAP3 Ensembl:ENSG00000132676 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1452872051 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136670,RMVar_hsa_circ_124226,RMVar_hsa_circ_320226,RMVar_hsa_circ_332365,RMVar_hsa_circ_317244,RMVar_hsa_circ_136679,RMVar_hsa_circ_111509,RMVar_hsa_circ_362272,RMVar_hsa_circ_365217,RMVar_hsa_circ_299789,RMVar_hsa_circ_314679,RMVar_hsa_circ_309024,RMVar_hsa_circ_59888,RMVar_hsa_circ_136681,RMVar_hsa_circ_136682,RMVar_hsa_circ_136683,RMVar_hsa_circ_136680 37146 RMVar_ID_37146 Human_SNP_ID_34774774 A-to-I Human chr1 + 155727425 155727425 155727425 CTAGGAGTTCAAGGTTACAGTGAACTGTGATCACATCCTGCCTTCTAGCCTGGGTGACAGAGCAA CTAGGAGTTCAAGGTTACAGTGAACTGTGATCGCATCCTGCCTTCTAGCCTGGGTGACAGAGCAA A G DAP3 Ensembl:ENSG00000132676 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1189617524 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2096364,Human_RBP_ID_3998239,Human_RBP_ID_5695411,Human_RBP_ID_9459522,Human_RBP_ID_10601091,Human_RBP_ID_22872725,Human_RBP_ID_24752739 RMVar_hsa_circ_136670,RMVar_hsa_circ_124226,RMVar_hsa_circ_320226,RMVar_hsa_circ_332365,RMVar_hsa_circ_317244,RMVar_hsa_circ_111509,RMVar_hsa_circ_362272,RMVar_hsa_circ_365217,RMVar_hsa_circ_299789,RMVar_hsa_circ_314679,RMVar_hsa_circ_309024,RMVar_hsa_circ_59888,RMVar_hsa_circ_136681,RMVar_hsa_circ_136682,RMVar_hsa_circ_136683,RMVar_hsa_circ_136680 37147 RMVar_ID_37147 Human_SNP_ID_34775540 A-to-I Human chr1 + 155730192 155730171 155730192 TATACCTATATGTTCATATATGTATATATAATATTCATATATGTATATATGTATATATAATATTC TATACCTATATG_____________________TTCATATATGTATATATGTATATATAATATTC GTTCATATATGTATATATAATA G DAP3 Ensembl:ENSG00000132676 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1557797565 Functional Loss DEL dbSNP153 13..33 33 - - - RMVar_hsa_circ_136670,RMVar_hsa_circ_124226,RMVar_hsa_circ_320226,RMVar_hsa_circ_111509,RMVar_hsa_circ_299789,RMVar_hsa_circ_59888,RMVar_hsa_circ_136682,RMVar_hsa_circ_136683,RMVar_hsa_circ_68767,RMVar_hsa_circ_49600 37148 RMVar_ID_37148 Human_SNP_ID_34775560 A-to-I Human chr1 + 155730192 155730190 155730193 TATACCTATATGTTCATATATGTATATATAATATTCATATATGTATATATGTATATATAATATTC TATACCTATATGTTCATATATGTATATATAA___TCATATATGTATATATGTATATATAATATTC ATAT A DAP3 Ensembl:ENSG00000132676 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1457222019 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_136670,RMVar_hsa_circ_124226,RMVar_hsa_circ_320226,RMVar_hsa_circ_111509,RMVar_hsa_circ_299789,RMVar_hsa_circ_59888,RMVar_hsa_circ_136682,RMVar_hsa_circ_136683,RMVar_hsa_circ_68767,RMVar_hsa_circ_49600 37149 RMVar_ID_37149 Human_SNP_ID_34776429 A-to-I Human chr1 + 155733714 155733714 155733714 TAAAAATTAGCCAGGTGTGGTGGTGCGTGCCTATAGTCCCAGTTACTCTGGAGGCTGAGGCAGAA TAAAAATTAGCCAGGTGTGGTGGTGCGTGCCTGTAGTCCCAGTTACTCTGGAGGCTGAGGCAGAA A G DAP3 Ensembl:ENSG00000132676 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs146023429 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111509,RMVar_hsa_circ_136683 37150 RMVar_ID_37150 Human_SNP_ID_34776437 A-to-I Human chr1 + 155733762 155733762 155733762 TGGAGGCTGAGGCAGAAGAATCGGTTGAACCCAGGAGGCGGAGGTTGCAGTGAACCAAGATTGTG TGGAGGCTGAGGCAGAAGAATCGGTTGAACCCCGGAGGCGGAGGTTGCAGTGAACCAAGATTGTG A C DAP3 Ensembl:ENSG00000132676 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1402597622 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10601206 RMVar_hsa_circ_111509,RMVar_hsa_circ_136683 37151 RMVar_ID_37151 Human_SNP_ID_34776532 A-to-I Human chr1 + 155734231 155734231 155734231 TAAAATGTCCCCATCATTATTTTTTTGGAGATAGGGTCTCACTCTGTCACCCAGGCTGTAGTGCA TAAAATGTCCCCATCATTATTTTTTTGGAGATGGGGTCTCACTCTGTCACCCAGGCTGTAGTGCA A G DAP3 Ensembl:ENSG00000132676 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1002267213 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8286850,Human_RBP_ID_17557343 RMVar_hsa_circ_111509,RMVar_hsa_circ_136683 37152 RMVar_ID_37152 Human_SNP_ID_34776691 A-to-I Human chr1 + 155735009 155735009 155735009 CTCTCAGGCTGGGCGTGGTGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCCGAGGCGGGCAG CTCTCAGGCTGGGCGTGGTGGCTCATGCCTATGATCCCAGCACTTTGGGAGGCCGAGGCGGGCAG A G DAP3 Ensembl:ENSG00000132676 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs752578712 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111509,RMVar_hsa_circ_136683 37153 RMVar_ID_37153 Human_SNP_ID_34776814 A-to-I Human chr1 + 155735320 155735317 155735320 TCCTTGGGCCGGGCGCAGTGGCTCACGCCTATAATCCCTGCACTTTGGGAGGCCAGGGCGGGCGG TCCTTGGGCCGGGCGCAGTGGCTCACGCCT___ATCCCTGCACTTTGGGAGGCCAGGGCGGGCGG TATA T DAP3 Ensembl:ENSG00000132676 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1436734671 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_802731,Human_RBP_ID_10601265 RMVar_hsa_circ_111509,RMVar_hsa_circ_136683 37154 RMVar_ID_37154 Human_SNP_ID_34776825 A-to-I Human chr1 + 155735356 155735356 155735356 CCTGCACTTTGGGAGGCCAGGGCGGGCGGATCACCTGAGGTCAGGAGTTCAAGACCAGCCTGGCC CCTGCACTTTGGGAGGCCAGGGCGGGCGGATCGCCTGAGGTCAGGAGTTCAAGACCAGCCTGGCC A G DAP3 Ensembl:ENSG00000132676 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs891933253 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111509,RMVar_hsa_circ_136683 37155 RMVar_ID_37155 Human_SNP_ID_34776833 A-to-I Human chr1 + 155735392 155735392 155735392 GAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGATGAAATCCTGTCTCTACTAAAAATACAAA GAGGTCAGGAGTTCAAGACCAGCCTGGCCAACGTGATGAAATCCTGTCTCTACTAAAAATACAAA A G DAP3 Ensembl:ENSG00000132676 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1010030414 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111509,RMVar_hsa_circ_136683 37156 RMVar_ID_37156 Human_SNP_ID_34776856 A-to-I Human chr1 + 155735483 155735483 155735483 CATGTAATGCCAGCTACTCGTGAGGCTGAGACAGGAGAATCGCTTGAACCCAGGAGGCAGAGGTT CATGTAATGCCAGCTACTCGTGAGGCTGAGACGGGAGAATCGCTTGAACCCAGGAGGCAGAGGTT A G DAP3 Ensembl:ENSG00000132676 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1263490852 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111509,RMVar_hsa_circ_136683 37157 RMVar_ID_37157 Human_SNP_ID_34776953 A-to-I Human chr1 + 155735905 155735905 155735905 TGCTCTGTCACCAGGCTGGAGTGCAGTGGCTTAATCTCGGCTCACTGCAACATCCACCTCCCGAG TGCTCTGTCACCAGGCTGGAGTGCAGTGGCTTTATCTCGGCTCACTGCAACATCCACCTCCCGAG A T DAP3 Ensembl:ENSG00000132676 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1438014787 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111509,RMVar_hsa_circ_136683 37158 RMVar_ID_37158 Human_SNP_ID_34777166 A-to-I Human chr1 + 155736651 155736651 155736651 ATGGCCCAGGCTCGTCTGGAACTCCTGGGCTCAAGCAATATGCCCATCTCAGCCTCCCAAGGTGC ATGGCCCAGGCTCGTCTGGAACTCCTGGGCTCCAGCAATATGCCCATCTCAGCCTCCCAAGGTGC A C DAP3 Ensembl:ENSG00000132676 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1174609014 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23144755,Human_RBP_ID_24593857 Human_Splice_Rec_139950,Human_Splice_Rec_139951 RMVar_hsa_circ_111509,RMVar_hsa_circ_136683 37159 RMVar_ID_37159 Human_SNP_ID_34777167 A-to-I Human chr1 + 155736655 155736655 155736655 CCCAGGCTCGTCTGGAACTCCTGGGCTCAAGCAATATGCCCATCTCAGCCTCCCAAGGTGCTGGG CCCAGGCTCGTCTGGAACTCCTGGGCTCAAGCCATATGCCCATCTCAGCCTCCCAAGGTGCTGGG A C DAP3 Ensembl:ENSG00000132676 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1478557011 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23144755,Human_RBP_ID_24593857 Human_Splice_Rec_139950,Human_Splice_Rec_139951 RMVar_hsa_circ_111509,RMVar_hsa_circ_136683 37160 RMVar_ID_37160 Human_SNP_ID_34777172 A-to-I Human chr1 + 155736669 155736669 155736669 GAACTCCTGGGCTCAAGCAATATGCCCATCTCAGCCTCCCAAGGTGCTGGGATTACAGGTGTGAG GAACTCCTGGGCTCAAGCAATATGCCCATCTCGGCCTCCCAAGGTGCTGGGATTACAGGTGTGAG A G DAP3 Ensembl:ENSG00000132676 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs996736920 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23144755,Human_RBP_ID_24593857 Human_Splice_Rec_139950,Human_Splice_Rec_139951 RMVar_hsa_circ_111509,RMVar_hsa_circ_136683 37161 RMVar_ID_37161 Human_SNP_ID_34777175 A-to-I Human chr1 + 155736677 155736677 155736677 GGGCTCAAGCAATATGCCCATCTCAGCCTCCCAAGGTGCTGGGATTACAGGTGTGAGTCACTGTG GGGCTCAAGCAATATGCCCATCTCAGCCTCCCTAGGTGCTGGGATTACAGGTGTGAGTCACTGTG A T DAP3 Ensembl:ENSG00000132676 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs890924870 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_139950,Human_Splice_Rec_139951 RMVar_hsa_circ_111509,RMVar_hsa_circ_136683 37162 RMVar_ID_37162 Human_SNP_ID_34779104 A-to-I Human chr1 - 155744287 155744287 155744287 CTCTCTTGCCCAGGCTGGTGTGCAGTGGTGCAATCTCGGCTGACCGCAGCCTCAACCTCTTGGGC CTCTCTTGCCCAGGCTGGTGTGCAGTGGTGCAGTCTCGGCTGACCGCAGCCTCAACCTCTTGGGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202202156 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 37163 RMVar_ID_37163 Human_SNP_ID_34781114 A-to-I Human chr1 + 155750863 155750863 155750863 TCAGCTTACTGCAACCTCCGTCTCCTGGGTTCAAGCAATTCTCCTGCCTCAGCCTTCAGAGTAGC TCAGCTTACTGCAACCTCCGTCTCCTGGGTTCGAGCAATTCTCCTGCCTCAGCCTTCAGAGTAGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1286371422 Functional Loss SNV dbSNP153 33..33 33 - - - 37164 RMVar_ID_37164 Human_SNP_ID_34781219 A-to-I Human chr1 + 155751368 155751368 155751368 AGGAGTTCAAGACTAGCCTTGCCAACATGGTGAAACCCCGTGTCTACTAAAAATAAATAAATTAG AGGAGTTCAAGACTAGCCTTGCCAACATGGTGGAACCCCGTGTCTACTAAAAATAAATAAATTAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs35927677 Functional Loss SNV dbSNP153 33..33 33 - - - 37165 RMVar_ID_37165 Human_SNP_ID_34781910 A-to-I Human chr1 - 155753668 155753667 155753669 TCTATCTTTTCTTTTTGTTTGTCATTTGAGACAGAGTCTCACTATGTTACCCAGGCTGATCTTGA TCTATCTTTTCTTTTTGTTTGTCATTTGAGA__GAGTCTCACTATGTTACCCAGGCTGATCTTGA CTG C GON4L Ensembl:ENSG00000116580 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1395273118 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,RMVar_hsa_circ_53480,RMVar_hsa_circ_321383,RMVar_hsa_circ_323617,RMVar_hsa_circ_17870 37166 RMVar_ID_37166 Human_SNP_ID_34781911 A-to-I Human chr1 - 155753668 155753668 155753668 TCTATCTTTTCTTTTTGTTTGTCATTTGAGACAGAGTCTCACTATGTTACCCAGGCTGATCTTGA TCTATCTTTTCTTTTTGTTTGTCATTTGAGACCGAGTCTCACTATGTTACCCAGGCTGATCTTGA T G GON4L Ensembl:ENSG00000116580 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1296713959 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,RMVar_hsa_circ_53480,RMVar_hsa_circ_321383,RMVar_hsa_circ_323617,RMVar_hsa_circ_17870 37167 RMVar_ID_37167 Human_SNP_ID_34784542 A-to-I Human chr1 - 155763989 155763989 155763989 TTGTTTTTGTTTTTGTTTTGAGATGGAGTCTTACTCTGTCTCCCGGATTGGAGTGCAGTGGCATA TTGTTTTTGTTTTTGTTTTGAGATGGAGTCTTTCTCTGTCTCCCGGATTGGAGTGCAGTGGCATA T A GON4L Ensembl:ENSG00000116580 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1475022587 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1726693 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_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 37168 RMVar_ID_37168 Human_SNP_ID_34788071 A-to-I Human chr1 - 155776718 155776718 155776718 TGAGACCCTGTCTCTGCAAAAAATAAAAATAAATTAGCCAGGCATGGTGCCATGCATCTGTGGTC TGAGACCCTGTCTCTGCAAAAAATAAAAATAAGTTAGCCAGGCATGGTGCCATGCATCTGTGGTC T C GON4L Ensembl:ENSG00000116580 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1339662325 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_6614,RMVar_hsa_circ_62122,RMVar_hsa_circ_53480,RMVar_hsa_circ_72995,RMVar_hsa_circ_62364,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_30860,RMVar_hsa_circ_67152,RMVar_hsa_circ_108586,RMVar_hsa_circ_136692,RMVar_hsa_circ_57488,RMVar_hsa_circ_60308,RMVar_hsa_circ_273958,RMVar_hsa_circ_62302,RMVar_hsa_circ_276923,RMVar_hsa_circ_136694,RMVar_hsa_circ_46340,RMVar_hsa_circ_58047,RMVar_hsa_circ_29349,RMVar_hsa_circ_26499,RMVar_hsa_circ_99162,RMVar_hsa_circ_136696,RMVar_hsa_circ_288839,RMVar_hsa_circ_373004,RMVar_hsa_circ_136700,RMVar_hsa_circ_136702,RMVar_hsa_circ_54906,RMVar_hsa_circ_136701,RMVar_hsa_circ_88356,RMVar_hsa_circ_336706,RMVar_hsa_circ_26814,RMVar_hsa_circ_357485,RMVar_hsa_circ_136703,RMVar_hsa_circ_331075,RMVar_hsa_circ_136705 37169 RMVar_ID_37169 Human_SNP_ID_34790835 A-to-I Human chr1 - 155787624 155787624 155787624 GGATTCCAGGTGCATGCCACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCAC GGATTCCAGGTGCATGCCACCATGCCTGGCTAGTTTTTGTATTTTTAGTAGAGACGGGGTTTCAC T C GON4L Ensembl:ENSG00000116580 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1004352841 Functional Loss SNV dbSNP153 33..33 33 - - - 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_54906,RMVar_hsa_circ_88356,RMVar_hsa_circ_136703,RMVar_hsa_circ_32199,RMVar_hsa_circ_286059,RMVar_hsa_circ_306921,RMVar_hsa_circ_75300 37170 RMVar_ID_37170 Human_SNP_ID_34791163 A-to-I Human chr1 - 155788990 155788990 155788990 CGCCTACCAGGTTCACGCCATTCTCCTGCCTCAGACTCCCGAGTAGCTGGGACTACAGGTGCCTG CGCCTACCAGGTTCACGCCATTCTCCTGCCTCGGACTCCCGAGTAGCTGGGACTACAGGTGCCTG T C GON4L Ensembl:ENSG00000116580 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1351193015 Functional Loss SNV dbSNP153 33..33 33 - - - 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_54906,RMVar_hsa_circ_88356,RMVar_hsa_circ_136703,RMVar_hsa_circ_32199,RMVar_hsa_circ_286059,RMVar_hsa_circ_306921,RMVar_hsa_circ_75300 37171 RMVar_ID_37171 Human_SNP_ID_34794835 A-to-I Human chr1 - 155803477 155803477 155803477 GCTCTTTGGGAGGCCGAGGCGGGCGGATCACAAGGTCAAGAGATTGAGACCATCCTGGCCAACAG GCTCTTTGGGAGGCCGAGGCGGGCGGATCACAGGGTCAAGAGATTGAGACCATCCTGGCCAACAG T C GON4L Ensembl:ENSG00000116580 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1308242816 Functional Loss SNV dbSNP153 33..33 33 - - - 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_306921,RMVar_hsa_circ_75300,RMVar_hsa_circ_269872,RMVar_hsa_circ_271767,RMVar_hsa_circ_29744,RMVar_hsa_circ_136707,RMVar_hsa_circ_136708,RMVar_hsa_circ_136709 37172 RMVar_ID_37172 Human_SNP_ID_34795348 A-to-I Human chr1 - 155805827 155805827 155805827 AAATTAGTCAGATGTCGTGGCTGGTGCCTGTAATCCCAGCTCCCTGGGAGGCTGAGGCAGGAGAA AAATTAGTCAGATGTCGTGGCTGGTGCCTGTAGTCCCAGCTCCCTGGGAGGCTGAGGCAGGAGAA T C GON4L Ensembl:ENSG00000116580 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1420062425 Functional Loss SNV dbSNP153 33..33 33 - - - 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 37173 RMVar_ID_37173 Human_SNP_ID_34797953 A-to-I Human chr1 - 155814921 155814921 155814921 TTTAGTAGAGATGGGGTTTCGCCATGTTGGCCAGGCTGGTCTCGGACTTCTGACCTCAAGTGATC TTTAGTAGAGATGGGGTTTCGCCATGTTGGCCGGGCTGGTCTCGGACTTCTGACCTCAAGTGATC T C GON4L Ensembl:ENSG00000116580 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006325734 Functional Loss SNV dbSNP153 33..33 33 - - - 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_99162,RMVar_hsa_circ_136702,RMVar_hsa_circ_88356,RMVar_hsa_circ_136703,RMVar_hsa_circ_75300,RMVar_hsa_circ_271767,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_18573,RMVar_hsa_circ_48407,RMVar_hsa_circ_136712,RMVar_hsa_circ_353337,RMVar_hsa_circ_363526,RMVar_hsa_circ_347757,RMVar_hsa_circ_64487 37174 RMVar_ID_37174 Human_SNP_ID_34798465 A-to-I Human chr1 - 155817034 155817034 155817034 AGTGAGCTCTGATTGTGCTGCTGCTCTAGCCTAGGCAACAGGGCAAGATCCTGTCTCAAAACAAA AGTGAGCTCTGATTGTGCTGCTGCTCTAGCCTGGGCAACAGGGCAAGATCCTGTCTCAAAACAAA T C GON4L Ensembl:ENSG00000116580 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1003307095 Functional Loss SNV dbSNP153 33..33 33 - - - 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_58047,RMVar_hsa_circ_75300,RMVar_hsa_circ_271767,RMVar_hsa_circ_60492,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_136712,RMVar_hsa_circ_353337,RMVar_hsa_circ_347757,RMVar_hsa_circ_64487,RMVar_hsa_circ_74432 37175 RMVar_ID_37175 Human_SNP_ID_34798516 A-to-I Human chr1 - 155817269 155817269 155817269 GTTCTTTAGGCTAGATGTGGTGGCTCACACCTATAATCCCAGTGCTTTGAGAGGCTAAGGTGGGA GTTCTTTAGGCTAGATGTGGTGGCTCACACCTGTAATCCCAGTGCTTTGAGAGGCTAAGGTGGGA T C GON4L Ensembl:ENSG00000116580 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs768029499 Functional Loss SNV dbSNP153 33..33 33 - - - 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_58047,RMVar_hsa_circ_75300,RMVar_hsa_circ_271767,RMVar_hsa_circ_60492,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_136712,RMVar_hsa_circ_353337,RMVar_hsa_circ_347757,RMVar_hsa_circ_64487,RMVar_hsa_circ_74432 37176 RMVar_ID_37176 Human_SNP_ID_34798851 A-to-I Human chr1 - 155818752 155818752 155818752 TGTGATCGCCCGCCTTGTCCTCCCAATGTGCTAGGATTACAGGCGTGAGCCACTGTGCCCGTCCC TGTGATCGCCCGCCTTGTCCTCCCAATGTGCTGGGATTACAGGCGTGAGCCACTGTGCCCGTCCC T C GON4L Ensembl:ENSG00000116580 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1012949527 Functional Loss SNV dbSNP153 33..33 33 - - - 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_58047,RMVar_hsa_circ_75300,RMVar_hsa_circ_271767,RMVar_hsa_circ_60492,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_136712,RMVar_hsa_circ_353337,RMVar_hsa_circ_347757,RMVar_hsa_circ_64487,RMVar_hsa_circ_74432 37177 RMVar_ID_37177 Human_SNP_ID_34798908 A-to-I Human chr1 - 155818984 155818984 155818984 TGCCTGGCCTTTTTGTTTTGAGATGGAGTCTCACTCTGTCACCTAGGCTGGAGTGCAGTGGTGCG TGCCTGGCCTTTTTGTTTTGAGATGGAGTCTCTCTCTGTCACCTAGGCTGGAGTGCAGTGGTGCG T A GON4L Ensembl:ENSG00000116580 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1187075055 Functional Loss SNV dbSNP153 33..33 33 - - - 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_58047,RMVar_hsa_circ_75300,RMVar_hsa_circ_271767,RMVar_hsa_circ_60492,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_136712,RMVar_hsa_circ_353337,RMVar_hsa_circ_347757,RMVar_hsa_circ_64487,RMVar_hsa_circ_74432 37178 RMVar_ID_37178 Human_SNP_ID_34798909 A-to-I Human chr1 - 155818984 155818984 155818984 TGCCTGGCCTTTTTGTTTTGAGATGGAGTCTCACTCTGTCACCTAGGCTGGAGTGCAGTGGTGCG TGCCTGGCCTTTTTGTTTTGAGATGGAGTCTCGCTCTGTCACCTAGGCTGGAGTGCAGTGGTGCG T C GON4L Ensembl:ENSG00000116580 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1187075055 Functional Loss SNV dbSNP153 33..33 33 - - - 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_58047,RMVar_hsa_circ_75300,RMVar_hsa_circ_271767,RMVar_hsa_circ_60492,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_136712,RMVar_hsa_circ_353337,RMVar_hsa_circ_347757,RMVar_hsa_circ_64487,RMVar_hsa_circ_74432 37179 RMVar_ID_37179 Human_SNP_ID_34801922 A-to-I Human chr1 - 155830644 155830644 155830644 AGGTTGAGGCCGCAGTGAGCTGAGATCGTACCACTGCACTTCAGCCTAGGGGACAGAGCGAGACC AGGTTGAGGCCGCAGTGAGCTGAGATCGTACCGCTGCACTTCAGCCTAGGGGACAGAGCGAGACC T C GON4L Ensembl:ENSG00000116580 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1257886616 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_348477,RMVar_hsa_circ_136712,RMVar_hsa_circ_71077,RMVar_hsa_circ_360729 37180 RMVar_ID_37180 Human_SNP_ID_34808429 A-to-I Human chr1 - 155855809 155855809 155855809 CCCGGCTAATTTTTGTATTTTTTAGTAGAGACAGCGTTTCACCATATTGACCAGGCTGGTCTCGA CCCGGCTAATTTTTGTATTTTTTAGTAGAGACGGCGTTTCACCATATTGACCAGGCTGGTCTCGA T C GON4L Ensembl:ENSG00000116580 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041888582 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136715 37181 RMVar_ID_37181 Human_SNP_ID_34814609 A-to-I Human chr1 + 155881910 155881910 155881910 ACGAGCATGCCCGGCTAATTTTTTGTATTTTCAGTAGAGATGGGTTTCACCATGTTGGCCAGGCT ACGAGCATGCCCGGCTAATTTTTTGTATTTTCGGTAGAGATGGGTTTCACCATGTTGGCCAGGCT A G SYT11 Ensembl:ENSG00000132718 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1205270173 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136719,RMVar_hsa_circ_136721 37182 RMVar_ID_37182 Human_SNP_ID_34814901 A-to-I Human chr1 + 155883428 155883428 155883428 GTGGTGCTGCACGCCTGTGGTCCCAGCTATTCAGGAGGCTGAGGTGGGAGGATCATTTGAGCCCA GTGGTGCTGCACGCCTGTGGTCCCAGCTATTCGGGAGGCTGAGGTGGGAGGATCATTTGAGCCCA A G SYT11 Ensembl:ENSG00000132718 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11548476 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136719,RMVar_hsa_circ_136721 37183 RMVar_ID_37183 Human_SNP_ID_34818744 A-to-I Human chr1 - 155899193 155899193 155899193 ATCTGAGCCTTGACCAAGTTTATCCTAAGGGAATACCACTTTGCTCCCTGTGCATAGTTTAGGAA ATCTGAGCCTTGACCAAGTTTATCCTAAGGGAGTACCACTTTGCTCCCTGTGCATAGTTTAGGAA T C RIT1 Ensembl:ENSG00000143622 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1055184 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22373482,Human_RBP_ID_23335689,Human_RBP_ID_26388661 GWAS_ID_4065,GWAS_ID_4066,GWAS_ID_4067,GWAS_ID_4068 37184 RMVar_ID_37184 Human_SNP_ID_34819532 A-to-I Human chr1 - 155902514 155902514 155902514 TGTTGTTTTTTAGACAGAGTTTCACTCTTATCACCCAGGCTGGAGTGCAGTGGCATGATGTTGGC TGTTGTTTTTTAGACAGAGTTTCACTCTTATCGCCCAGGCTGGAGTGCAGTGGCATGATGTTGGC T C RIT1 Ensembl:ENSG00000143622 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs899816889 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136722 37185 RMVar_ID_37185 Human_SNP_ID_34819904 A-to-I Human chr1 - 155903829 155903826 155903830 ATTGTTTTTACTTTTTGTGGAGACAGGATCTCACTATGTTGCCCAGGCTGATCTTGAACACCTGG ATTGTTTTTACTTTTTGTGGAGACAGGATCT____ATGTTGCCCAGGCTGATCTTGAACACCTGG TAGTG T RIT1 Ensembl:ENSG00000143622 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs967368489 Functional Loss DEL dbSNP153 32..35 33 - - - RMVar_hsa_circ_136722 37186 RMVar_ID_37186 Human_SNP_ID_34820363 A-to-I Human chr1 - 155905472 155905472 155905472 GTCTCGGCTGAGTGCAGTGGCCCACACCTGTAATACCAGCACTTTGGGAGGCCAAGGCAGGAGGA GTCTCGGCTGAGTGCAGTGGCCCACACCTGTAGTACCAGCACTTTGGGAGGCCAAGGCAGGAGGA T C RIT1 Ensembl:ENSG00000143622 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223490197 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24746946 RMVar_hsa_circ_81183,RMVar_hsa_circ_136724 37187 RMVar_ID_37187 Human_SNP_ID_34820735 A-to-I Human chr1 - 155906921 155906921 155906921 TTGGATTTTTAGTAGAGATGAGGTCTCGCTCTATTGCCCAGGCTGGTCTCAAACTCCTGAGCGCA TTGGATTTTTAGTAGAGATGAGGTCTCGCTCTGTTGCCCAGGCTGGTCTCAAACTCCTGAGCGCA T C RIT1 Ensembl:ENSG00000143622 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs942595621 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81183,RMVar_hsa_circ_136724 37188 RMVar_ID_37188 Human_SNP_ID_34820768 A-to-I Human chr1 - 155907070 155907070 155907070 AGGGTCTCACTCTGTTGCCCATGCTGGAGTGCAGTGTTGTGATCTTGGCTCACTGCAGCCTGGAC AGGGTCTCACTCTGTTGCCCATGCTGGAGTGCGGTGTTGTGATCTTGGCTCACTGCAGCCTGGAC T C RIT1 Ensembl:ENSG00000143622 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1046068708 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81183,RMVar_hsa_circ_136724 37189 RMVar_ID_37189 Human_SNP_ID_34820871 A-to-I Human chr1 - 155907439 155907439 155907439 CAGGAGTTCAAGACCAGCCTGGCCAACATGGTAAAACCCCATCTCTACTGAAAATACAAAAATTA CAGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTGAAAATACAAAAATTA T C RIT1 Ensembl:ENSG00000143622 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1439575772 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81183,RMVar_hsa_circ_136724 37190 RMVar_ID_37190 Human_SNP_ID_34821004 A-to-I Human chr1 - 155907978 155907978 155907978 TCATGCCATTCTCCTGCCTCAGGCTCCAGCGTAGCTGGGACTACAGGCACCCGCCACCTCGCCTG TCATGCCATTCTCCTGCCTCAGGCTCCAGCGTGGCTGGGACTACAGGCACCCGCCACCTCGCCTG T C RIT1 Ensembl:ENSG00000143622 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs656247 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81183,RMVar_hsa_circ_136724 37191 RMVar_ID_37191 Human_SNP_ID_34821035 A-to-I Human chr1 - 155908054 155908054 155908054 ATGGAGTCTCACTGTCGCCCAGGCTAGAGTGCAGTGGCATGATCTCGGCTCACTGCAGGCTCCGC ATGGAGTCTCACTGTCGCCCAGGCTAGAGTGCGGTGGCATGATCTCGGCTCACTGCAGGCTCCGC T C RIT1 Ensembl:ENSG00000143622 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1405883771 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81183,RMVar_hsa_circ_136724 37192 RMVar_ID_37192 Human_SNP_ID_34821226 A-to-I Human chr1 - 155908626 155908626 155908626 CCTGGGAGGCGGAGGTTGCAGTGAGCCGAGATAGTGCCATCACACTCCAGCCTGGGGGATAAGAG CCTGGGAGGCGGAGGTTGCAGTGAGCCGAGATGGTGCCATCACACTCCAGCCTGGGGGATAAGAG T C RIT1 Ensembl:ENSG00000143622 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs571339160 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81183,RMVar_hsa_circ_136724 37193 RMVar_ID_37193 Human_SNP_ID_34821247 A-to-I Human chr1 - 155908700 155908700 155908700 AAACTAGCCGGGCGTGGTGCTGGGTGCCTGTAATCCCAGCTACTGCGGGGGCTGAGGCAGGAGAA AAACTAGCCGGGCGTGGTGCTGGGTGCCTGTAGTCCCAGCTACTGCGGGGGCTGAGGCAGGAGAA T C RIT1 Ensembl:ENSG00000143622 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1306986063 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81183,RMVar_hsa_circ_136724 37194 RMVar_ID_37194 Human_SNP_ID_34821299 A-to-I Human chr1 - 155908858 155908858 155908858 CAAATTTAGAACACTGTTCAGAGATTCAGGCCAGGCGCGGTGGCTCATGCCTGTAATCCCAGCAC CAAATTTAGAACACTGTTCAGAGATTCAGGCCGGGCGCGGTGGCTCATGCCTGTAATCCCAGCAC T C RIT1 Ensembl:ENSG00000143622 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs553099179 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10603008 RMVar_hsa_circ_81183,RMVar_hsa_circ_136724 37195 RMVar_ID_37195 Human_SNP_ID_34823098 A-to-I Human chr1 - 155915513 155915510 155915514 ATAGAGCAAGACTCCATCTCATAAATAAATAAATACATAAATAAAGCTATTAATTTTCTAACCTG ATAGAGCAAGACTCCATCTCATAAATAAATA____CATAAATAAAGCTATTAATTTTCTAACCTG GTATT G KHDC4 Ensembl:ENSG00000132680 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs917305870 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_2096573,Human_RBP_ID_3282907,Human_RBP_ID_8043724,Human_RBP_ID_9459724,Human_RBP_ID_16970187,Human_RBP_ID_17727098,Human_RBP_ID_22872784,Human_RBP_ID_24752882 RMVar_hsa_circ_117053,RMVar_hsa_circ_136725 37196 RMVar_ID_37196 Human_SNP_ID_34823737 A-to-I Human chr1 - 155917981 155917981 155917981 TAACAGAAAGCTTATTACAGAAAGCTAATCACATCGACTGTCAGTGGTTGGAGTTCTGTTTGTTA TAACAGAAAGCTTATTACAGAAAGCTAATCACGTCGACTGTCAGTGGTTGGAGTTCTGTTTGTTA T C KHDC4 Ensembl:ENSG00000132680 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs605025 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_328397 GWAS_ID_4069,GWAS_ID_4070,GWAS_ID_4071,GWAS_ID_4072,GWAS_ID_4073,GWAS_ID_4074,GWAS_ID_4075,GWAS_ID_4076 RMVar_hsa_circ_117053,RMVar_hsa_circ_55665,RMVar_hsa_circ_136725,RMVar_hsa_circ_298499,RMVar_hsa_circ_66635,RMVar_hsa_circ_55113,RMVar_hsa_circ_97864,RMVar_hsa_circ_127665,RMVar_hsa_circ_136726,RMVar_hsa_circ_136727,RMVar_hsa_circ_136728,RMVar_hsa_circ_75533 37197 RMVar_ID_37197 Human_SNP_ID_34824047 A-to-I Human chr1 - 155919171 155919171 155919171 TTGAGGTCAGGAGTTCAAGACCAGCCTGGTCAACATGGTGAAACCCTGTCTCTGCTAAAAATACA TTGAGGTCAGGAGTTCAAGACCAGCCTGGTCAGCATGGTGAAACCCTGTCTCTGCTAAAAATACA T C KHDC4 Ensembl:ENSG00000132680 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1557966874 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24594528 RMVar_hsa_circ_117053,RMVar_hsa_circ_55665,RMVar_hsa_circ_136725,RMVar_hsa_circ_298499,RMVar_hsa_circ_66635,RMVar_hsa_circ_55113,RMVar_hsa_circ_97864,RMVar_hsa_circ_127665,RMVar_hsa_circ_136726,RMVar_hsa_circ_136727,RMVar_hsa_circ_136728,RMVar_hsa_circ_75533 37198 RMVar_ID_37198 Human_SNP_ID_34824138 A-to-I Human chr1 - 155919563 155919563 155919563 CTCGTGATCCGCCCACCTCAGACTCCCAAAGTACTGGGATTACAGGCGTGAGCCACCGCGCCCGG CTCGTGATCCGCCCACCTCAGACTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCCCGG T C KHDC4 Ensembl:ENSG00000132680 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1018372350 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117053,RMVar_hsa_circ_55665,RMVar_hsa_circ_136725,RMVar_hsa_circ_298499,RMVar_hsa_circ_66635,RMVar_hsa_circ_55113,RMVar_hsa_circ_97864,RMVar_hsa_circ_127665,RMVar_hsa_circ_136726,RMVar_hsa_circ_136727,RMVar_hsa_circ_136728,RMVar_hsa_circ_75533 37199 RMVar_ID_37199 Human_SNP_ID_34824179 A-to-I Human chr1 - 155919735 155919735 155919735 ACCATCTTGGCTCACTGCAAGCTCCGCCTCCCAGGTTCACGCGATTCTCCTGCCTCAGCCTCCCG ACCATCTTGGCTCACTGCAAGCTCCGCCTCCCTGGTTCACGCGATTCTCCTGCCTCAGCCTCCCG T A KHDC4 Ensembl:ENSG00000132680 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1210296217 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117053,RMVar_hsa_circ_55665,RMVar_hsa_circ_136725,RMVar_hsa_circ_298499,RMVar_hsa_circ_66635,RMVar_hsa_circ_55113,RMVar_hsa_circ_97864,RMVar_hsa_circ_127665,RMVar_hsa_circ_136726,RMVar_hsa_circ_136727,RMVar_hsa_circ_136728,RMVar_hsa_circ_75533 37200 RMVar_ID_37200 Human_SNP_ID_34824180 A-to-I Human chr1 - 155919735 155919735 155919735 ACCATCTTGGCTCACTGCAAGCTCCGCCTCCCAGGTTCACGCGATTCTCCTGCCTCAGCCTCCCG ACCATCTTGGCTCACTGCAAGCTCCGCCTCCCGGGTTCACGCGATTCTCCTGCCTCAGCCTCCCG T C KHDC4 Ensembl:ENSG00000132680 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1210296217 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117053,RMVar_hsa_circ_55665,RMVar_hsa_circ_136725,RMVar_hsa_circ_298499,RMVar_hsa_circ_66635,RMVar_hsa_circ_55113,RMVar_hsa_circ_97864,RMVar_hsa_circ_127665,RMVar_hsa_circ_136726,RMVar_hsa_circ_136727,RMVar_hsa_circ_136728,RMVar_hsa_circ_75533 37201 RMVar_ID_37201 Human_SNP_ID_34824467 A-to-I Human chr1 - 155920612 155920612 155920612 CCCTTGAGCCTAGGAGGTCATGGATGCAGTGAACCAAGATGGTGCCAGTGCACTCCAGCCTCAGT CCCTTGAGCCTAGGAGGTCATGGATGCAGTGAGCCAAGATGGTGCCAGTGCACTCCAGCCTCAGT T C KHDC4 Ensembl:ENSG00000132680 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1338074739 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117053,RMVar_hsa_circ_55665,RMVar_hsa_circ_136725,RMVar_hsa_circ_298499,RMVar_hsa_circ_66635,RMVar_hsa_circ_55113,RMVar_hsa_circ_97864,RMVar_hsa_circ_127665,RMVar_hsa_circ_136726,RMVar_hsa_circ_136727,RMVar_hsa_circ_136728,RMVar_hsa_circ_75533 37202 RMVar_ID_37202 Human_SNP_ID_34824475 A-to-I Human chr1 - 155920665 155920665 155920665 CATGGTGGCACATACCTGTATTTCAGCTACTTAAGAGGCTGAGATGGAAGGGTCCCTTGAGCCTA CATGGTGGCACATACCTGTATTTCAGCTACTTGAGAGGCTGAGATGGAAGGGTCCCTTGAGCCTA T C KHDC4 Ensembl:ENSG00000132680 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs562441850 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117053,RMVar_hsa_circ_55665,RMVar_hsa_circ_136725,RMVar_hsa_circ_298499,RMVar_hsa_circ_66635,RMVar_hsa_circ_55113,RMVar_hsa_circ_97864,RMVar_hsa_circ_127665,RMVar_hsa_circ_136726,RMVar_hsa_circ_136727,RMVar_hsa_circ_136728,RMVar_hsa_circ_75533 37203 RMVar_ID_37203 Human_SNP_ID_34824510 A-to-I Human chr1 - 155920800 155920800 155920800 AGTTAGCATTTCAAATCTTAGAAGGAAACATAATCTCAGCATCTGGGGAGGCCGAGGCAGGATTG AGTTAGCATTTCAAATCTTAGAAGGAAACATAGTCTCAGCATCTGGGGAGGCCGAGGCAGGATTG T C KHDC4 Ensembl:ENSG00000132680 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1157957890 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117053,RMVar_hsa_circ_55665,RMVar_hsa_circ_136725,RMVar_hsa_circ_298499,RMVar_hsa_circ_66635,RMVar_hsa_circ_55113,RMVar_hsa_circ_97864,RMVar_hsa_circ_127665,RMVar_hsa_circ_136726,RMVar_hsa_circ_136727,RMVar_hsa_circ_136728,RMVar_hsa_circ_75533 37204 RMVar_ID_37204 Human_SNP_ID_34824974 A-to-I Human chr1 - 155922284 155922284 155922284 AAAACTAGCTGGGTGCGGTGGCACGCGCCTGTAGTCCCAGCTACTTGGGAGGCTGAAGCAGGAGA AAAACTAGCTGGGTGCGGTGGCACGCGCCTGTGGTCCCAGCTACTTGGGAGGCTGAAGCAGGAGA T C KHDC4 Ensembl:ENSG00000132680 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs976675948 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117053,RMVar_hsa_circ_55665,RMVar_hsa_circ_136725,RMVar_hsa_circ_66635,RMVar_hsa_circ_55113,RMVar_hsa_circ_74417,RMVar_hsa_circ_97864,RMVar_hsa_circ_136727,RMVar_hsa_circ_285323,RMVar_hsa_circ_298880,RMVar_hsa_circ_272851,RMVar_hsa_circ_108867,RMVar_hsa_circ_125324,RMVar_hsa_circ_101961,RMVar_hsa_circ_136732,RMVar_hsa_circ_136734,RMVar_hsa_circ_136735,RMVar_hsa_circ_136733,RMVar_hsa_circ_136731 37205 RMVar_ID_37205 Human_SNP_ID_34825010 A-to-I Human chr1 - 155922396 155922396 155922396 TCATGCCTGTAATCCCAGCCCTTTGGGAGGCCAAGGCGGGCAGATAATGAGGTCAGGAGTTCGAG TCATGCCTGTAATCCCAGCCCTTTGGGAGGCCGAGGCGGGCAGATAATGAGGTCAGGAGTTCGAG T C KHDC4 Ensembl:ENSG00000132680 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs988162958 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117053,RMVar_hsa_circ_55665,RMVar_hsa_circ_136725,RMVar_hsa_circ_66635,RMVar_hsa_circ_55113,RMVar_hsa_circ_74417,RMVar_hsa_circ_97864,RMVar_hsa_circ_136727,RMVar_hsa_circ_285323,RMVar_hsa_circ_298880,RMVar_hsa_circ_272851,RMVar_hsa_circ_108867,RMVar_hsa_circ_125324,RMVar_hsa_circ_101961,RMVar_hsa_circ_136732,RMVar_hsa_circ_136734,RMVar_hsa_circ_136735,RMVar_hsa_circ_136733,RMVar_hsa_circ_136731 37206 RMVar_ID_37206 Human_SNP_ID_34825017 A-to-I Human chr1 - 155922417 155922417 155922417 AGGTGGGTTGGACACGGTGGCTCATGCCTGTAATCCCAGCCCTTTGGGAGGCCAAGGCGGGCAGA AGGTGGGTTGGACACGGTGGCTCATGCCTGTATTCCCAGCCCTTTGGGAGGCCAAGGCGGGCAGA T A KHDC4 Ensembl:ENSG00000132680 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs966039218 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117053,RMVar_hsa_circ_55665,RMVar_hsa_circ_136725,RMVar_hsa_circ_66635,RMVar_hsa_circ_55113,RMVar_hsa_circ_74417,RMVar_hsa_circ_97864,RMVar_hsa_circ_136727,RMVar_hsa_circ_285323,RMVar_hsa_circ_298880,RMVar_hsa_circ_272851,RMVar_hsa_circ_108867,RMVar_hsa_circ_125324,RMVar_hsa_circ_101961,RMVar_hsa_circ_136732,RMVar_hsa_circ_136734,RMVar_hsa_circ_136735,RMVar_hsa_circ_136733,RMVar_hsa_circ_136731 37207 RMVar_ID_37207 Human_SNP_ID_34825467 A-to-I Human chr1 - 155924205 155924191 155924206 ATTCTGTCGCCTCCTGCCTCAGCGTCCCAAGTAGCTGGGACTATAGGCACCCGCCAACATGCCCG ATTCTGTCGCCTCCTGCCTCAGCGTCCCAAG_______________GCACCCGCCAACATGCCCG CCTATAGTCCCAGCTA C KHDC4 Ensembl:ENSG00000132680 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs547368930 Functional Loss DEL dbSNP153 32..46 33 - - - RMVar_hsa_circ_117053,RMVar_hsa_circ_55665,RMVar_hsa_circ_136725,RMVar_hsa_circ_66635,RMVar_hsa_circ_55113,RMVar_hsa_circ_74417,RMVar_hsa_circ_97864,RMVar_hsa_circ_136727,RMVar_hsa_circ_285323,RMVar_hsa_circ_298880,RMVar_hsa_circ_108867,RMVar_hsa_circ_125324,RMVar_hsa_circ_101961,RMVar_hsa_circ_136732,RMVar_hsa_circ_136734,RMVar_hsa_circ_136735,RMVar_hsa_circ_136733,RMVar_hsa_circ_334796,RMVar_hsa_circ_376919 37208 RMVar_ID_37208 Human_SNP_ID_34825468 A-to-I Human chr1 - 155924195 155924195 155924195 CTCCTGCCTCAGCGTCCCAAGTAGCTGGGACTATAGGCACCCGCCAACATGCCCGGCTAATTTTT CTCCTGCCTCAGCGTCCCAAGTAGCTGGGACTGTAGGCACCCGCCAACATGCCCGGCTAATTTTT T C KHDC4 Ensembl:ENSG00000132680 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1464322612 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117053,RMVar_hsa_circ_55665,RMVar_hsa_circ_136725,RMVar_hsa_circ_66635,RMVar_hsa_circ_55113,RMVar_hsa_circ_74417,RMVar_hsa_circ_97864,RMVar_hsa_circ_136727,RMVar_hsa_circ_285323,RMVar_hsa_circ_298880,RMVar_hsa_circ_108867,RMVar_hsa_circ_125324,RMVar_hsa_circ_101961,RMVar_hsa_circ_136732,RMVar_hsa_circ_136734,RMVar_hsa_circ_136735,RMVar_hsa_circ_136733,RMVar_hsa_circ_334796,RMVar_hsa_circ_376919 37209 RMVar_ID_37209 Human_SNP_ID_34825537 A-to-I Human chr1 - 155924413 155924413 155924413 GGTCAGGAGATTGAGACCATCCTGGCTAATACAGTGAAATCCCGTTTCTACTAAAAATAAAACAA GGTCAGGAGATTGAGACCATCCTGGCTAATACGGTGAAATCCCGTTTCTACTAAAAATAAAACAA T C KHDC4 Ensembl:ENSG00000132680 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs763120030 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117053,RMVar_hsa_circ_55665,RMVar_hsa_circ_136725,RMVar_hsa_circ_66635,RMVar_hsa_circ_55113,RMVar_hsa_circ_74417,RMVar_hsa_circ_97864,RMVar_hsa_circ_136727,RMVar_hsa_circ_285323,RMVar_hsa_circ_298880,RMVar_hsa_circ_108867,RMVar_hsa_circ_125324,RMVar_hsa_circ_101961,RMVar_hsa_circ_136732,RMVar_hsa_circ_136734,RMVar_hsa_circ_136735,RMVar_hsa_circ_136733,RMVar_hsa_circ_334796,RMVar_hsa_circ_376919 37210 RMVar_ID_37210 Human_SNP_ID_34825807 A-to-I Human chr1 - 155925233 155925233 155925233 AGGTCAGGAGATCGAGACCATCCTGGCTAACAAGGTGAAACCCCGTCTCTACTAAAAATAAAACA AGGTCAGGAGATCGAGACCATCCTGGCTAACAGGGTGAAACCCCGTCTCTACTAAAAATAAAACA T C KHDC4 Ensembl:ENSG00000132680 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1017901314 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_96931 RMVar_hsa_circ_117053,RMVar_hsa_circ_55665,RMVar_hsa_circ_136725,RMVar_hsa_circ_66635,RMVar_hsa_circ_55113,RMVar_hsa_circ_74417,RMVar_hsa_circ_97864,RMVar_hsa_circ_136727,RMVar_hsa_circ_285323,RMVar_hsa_circ_298880,RMVar_hsa_circ_108867,RMVar_hsa_circ_125324,RMVar_hsa_circ_101961,RMVar_hsa_circ_136732,RMVar_hsa_circ_136734,RMVar_hsa_circ_136735,RMVar_hsa_circ_136733,RMVar_hsa_circ_334796,RMVar_hsa_circ_376919 37211 RMVar_ID_37211 Human_SNP_ID_34825808 A-to-I Human chr1 - 155925233 155925233 155925233 AGGTCAGGAGATCGAGACCATCCTGGCTAACAAGGTGAAACCCCGTCTCTACTAAAAATAAAACA AGGTCAGGAGATCGAGACCATCCTGGCTAACACGGTGAAACCCCGTCTCTACTAAAAATAAAACA T G KHDC4 Ensembl:ENSG00000132680 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1017901314 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_96931 RMVar_hsa_circ_117053,RMVar_hsa_circ_55665,RMVar_hsa_circ_136725,RMVar_hsa_circ_66635,RMVar_hsa_circ_55113,RMVar_hsa_circ_74417,RMVar_hsa_circ_97864,RMVar_hsa_circ_136727,RMVar_hsa_circ_285323,RMVar_hsa_circ_298880,RMVar_hsa_circ_108867,RMVar_hsa_circ_125324,RMVar_hsa_circ_101961,RMVar_hsa_circ_136732,RMVar_hsa_circ_136734,RMVar_hsa_circ_136735,RMVar_hsa_circ_136733,RMVar_hsa_circ_334796,RMVar_hsa_circ_376919 37212 RMVar_ID_37212 Human_SNP_ID_34827451 A-to-I Human chr1 - 155930344 155930344 155930344 TTATTGACTTTATTTAATGTCATTTTAGTGAGATTTTTGTTTGCTTGTTAATTCGTTTATGAAGA TTATTGACTTTATTTAATGTCATTTTAGTGAGGTTTTTGTTTGCTTGTTAATTCGTTTATGAAGA T C KHDC4 Ensembl:ENSG00000132680 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs3768280 Functional Loss SNV dbSNP153,JSNP 33..33 33 - - - Human_RBP_ID_10603786 GWAS_ID_4077,GWAS_ID_4078,GWAS_ID_4079,GWAS_ID_4080,GWAS_ID_4081,GWAS_ID_4082,GWAS_ID_4083,GWAS_ID_4084 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 37213 RMVar_ID_37213 Human_SNP_ID_34828058 A-to-I Human chr1 - 155932877 155932877 155932877 GAAGTGCAGTAGTGGGGTGATCTCGGCTCACTACAACCTCTGTCTCCTGGGTTCAAGTGATTCTG GAAGTGCAGTAGTGGGGTGATCTCGGCTCACTGCAACCTCTGTCTCCTGGGTTCAAGTGATTCTG T C KHDC4 Ensembl:ENSG00000132680 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1038888493 Functional Loss SNV dbSNP153 33..33 33 - - - 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 37214 RMVar_ID_37214 Human_SNP_ID_34829812 A-to-I Human chr1 - 155939625 155939625 155939625 CCTACCTCAGCCACAGGAATGTGCTACCACACAGGCTAATTTTTGTATTTTTAGGAGAGATGGGG CCTACCTCAGCCACAGGAATGTGCTACCACACGGGCTAATTTTTGTATTTTTAGGAGAGATGGGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs750242095 Functional Loss SNV dbSNP153 33..33 33 - - - 37215 RMVar_ID_37215 Human_SNP_ID_34834291 A-to-I Human chr1 - 155956639 155956639 155956639 TTTTGTATTTTTAGTGGAGACGGGGTTTTGCCATGTTGACCAAGCTGGTCTCGAACTCCTGATCT TTTTGTATTTTTAGTGGAGACGGGGTTTTGCCGTGTTGACCAAGCTGGTCTCGAACTCCTGATCT T C ARHGEF2 Ensembl:ENSG00000116584 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1202846870 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39461,RMVar_hsa_circ_120830,RMVar_hsa_circ_116735,RMVar_hsa_circ_122212,RMVar_hsa_circ_136741,RMVar_hsa_circ_136742,RMVar_hsa_circ_322943,RMVar_hsa_circ_136743,RMVar_hsa_circ_136744 37216 RMVar_ID_37216 Human_SNP_ID_34834327 A-to-I Human chr1 - 155956812 155956812 155956812 AGCTGGGACTACAGGCTCACGCCACCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGT AGCTGGGACTACAGGCTCACGCCACCATGCCCGGCTAATTTTTGTATTTTTAGTAGAGACGGGGT T C ARHGEF2 Ensembl:ENSG00000116584 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs944209231 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39461,RMVar_hsa_circ_120830,RMVar_hsa_circ_116735,RMVar_hsa_circ_122212,RMVar_hsa_circ_136741,RMVar_hsa_circ_136742,RMVar_hsa_circ_322943,RMVar_hsa_circ_136743,RMVar_hsa_circ_136744 37217 RMVar_ID_37217 Human_SNP_ID_34834331 A-to-I Human chr1 - 155956834 155956832 155956835 GGGCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCTCACGCCACCATGCCCAGCTAATTTTT GGGCTGCCTCAGCCTCCTGAGTAGCTGGGAC___AGGCTCACGCCACCATGCCCAGCTAATTTTT TGTA T ARHGEF2 Ensembl:ENSG00000116584 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1162466353 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_39461,RMVar_hsa_circ_120830,RMVar_hsa_circ_116735,RMVar_hsa_circ_122212,RMVar_hsa_circ_136741,RMVar_hsa_circ_136742,RMVar_hsa_circ_322943,RMVar_hsa_circ_136743,RMVar_hsa_circ_136744 37218 RMVar_ID_37218 Human_SNP_ID_34835048 A-to-I Human chr1 - 155959701 155959700 155959701 ATCTCTACTAAAAATACAAAAATTAGCCAGGCATGGCAGCATTCACCTGTAGCCACAGCTACTTG ATCTCTACTAAAAATACAAAAATTAGCCAGGC_TGGCAGCATTCACCTGTAGCCACAGCTACTTG AT A ARHGEF2 Ensembl:ENSG00000116584 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs869161962 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_39461,RMVar_hsa_circ_120830,RMVar_hsa_circ_40268,RMVar_hsa_circ_116735,RMVar_hsa_circ_122212,RMVar_hsa_circ_136741,RMVar_hsa_circ_136742,RMVar_hsa_circ_73347,RMVar_hsa_circ_136744,RMVar_hsa_circ_369785,RMVar_hsa_circ_136746,RMVar_hsa_circ_109653,RMVar_hsa_circ_136747 37219 RMVar_ID_37219 Human_SNP_ID_34835049 A-to-I Human chr1 - 155959701 155959701 155959701 ATCTCTACTAAAAATACAAAAATTAGCCAGGCATGGCAGCATTCACCTGTAGCCACAGCTACTTG ATCTCTACTAAAAATACAAAAATTAGCCAGGCTTGGCAGCATTCACCTGTAGCCACAGCTACTTG T A ARHGEF2 Ensembl:ENSG00000116584 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4661169 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39461,RMVar_hsa_circ_120830,RMVar_hsa_circ_40268,RMVar_hsa_circ_116735,RMVar_hsa_circ_122212,RMVar_hsa_circ_136741,RMVar_hsa_circ_136742,RMVar_hsa_circ_73347,RMVar_hsa_circ_136744,RMVar_hsa_circ_369785,RMVar_hsa_circ_136746,RMVar_hsa_circ_109653,RMVar_hsa_circ_136747 37220 RMVar_ID_37220 Human_SNP_ID_34835050 A-to-I Human chr1 - 155959701 155959701 155959701 ATCTCTACTAAAAATACAAAAATTAGCCAGGCATGGCAGCATTCACCTGTAGCCACAGCTACTTG ATCTCTACTAAAAATACAAAAATTAGCCAGGCGTGGCAGCATTCACCTGTAGCCACAGCTACTTG T C ARHGEF2 Ensembl:ENSG00000116584 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4661169 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39461,RMVar_hsa_circ_120830,RMVar_hsa_circ_40268,RMVar_hsa_circ_116735,RMVar_hsa_circ_122212,RMVar_hsa_circ_136741,RMVar_hsa_circ_136742,RMVar_hsa_circ_73347,RMVar_hsa_circ_136744,RMVar_hsa_circ_369785,RMVar_hsa_circ_136746,RMVar_hsa_circ_109653,RMVar_hsa_circ_136747 37221 RMVar_ID_37221 Human_SNP_ID_34835181 A-to-I Human chr1 - 155960303 155960303 155960303 CACCACACCCAGCACATTTTTAAATTTTTTGTAGAGATAAGATCTTGCTATGTTGCCTAGGCTAG CACCACACCCAGCACATTTTTAAATTTTTTGTGGAGATAAGATCTTGCTATGTTGCCTAGGCTAG T C ARHGEF2 Ensembl:ENSG00000116584 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1016255874 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39461,RMVar_hsa_circ_120830,RMVar_hsa_circ_40268,RMVar_hsa_circ_116735,RMVar_hsa_circ_122212,RMVar_hsa_circ_136741,RMVar_hsa_circ_136742,RMVar_hsa_circ_73347,RMVar_hsa_circ_136744,RMVar_hsa_circ_369785,RMVar_hsa_circ_136746,RMVar_hsa_circ_109653,RMVar_hsa_circ_136747 37222 RMVar_ID_37222 Human_SNP_ID_34835201 A-to-I Human chr1 - 155960416 155960416 155960416 CTGCTCAGGCTGGGGTGCAGTGGTGCAGTCATAGCTCACTGTAACTCAAACTCCTGGGCTCAAGT CTGCTCAGGCTGGGGTGCAGTGGTGCAGTCATTGCTCACTGTAACTCAAACTCCTGGGCTCAAGT T A ARHGEF2 Ensembl:ENSG00000116584 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1465739217 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39461,RMVar_hsa_circ_120830,RMVar_hsa_circ_40268,RMVar_hsa_circ_116735,RMVar_hsa_circ_122212,RMVar_hsa_circ_136741,RMVar_hsa_circ_136742,RMVar_hsa_circ_73347,RMVar_hsa_circ_136744,RMVar_hsa_circ_369785,RMVar_hsa_circ_136746,RMVar_hsa_circ_109653,RMVar_hsa_circ_136747 37223 RMVar_ID_37223 Human_SNP_ID_34836101 A-to-I Human chr1 - 155963810 155963810 155963810 AAAACTAGTCAGGTGTGGTGGCATGTGCCTATAGTCCCAGCTACTTGGGAGGCTGAGACAGGAGG AAAACTAGTCAGGTGTGGTGGCATGTGCCTATGGTCCCAGCTACTTGGGAGGCTGAGACAGGAGG T C ARHGEF2 Ensembl:ENSG00000116584 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs990680170 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120830,RMVar_hsa_circ_9728,RMVar_hsa_circ_40268,RMVar_hsa_circ_116735,RMVar_hsa_circ_122212,RMVar_hsa_circ_136741,RMVar_hsa_circ_136742,RMVar_hsa_circ_73347,RMVar_hsa_circ_136744,RMVar_hsa_circ_109653,RMVar_hsa_circ_114785,RMVar_hsa_circ_136747,RMVar_hsa_circ_360636,RMVar_hsa_circ_88908,RMVar_hsa_circ_136748,RMVar_hsa_circ_136749 37224 RMVar_ID_37224 Human_SNP_ID_34843154 A-to-I Human chr1 - 155992387 155992387 155992387 CTGTAGGCCTAGCTACTCGGGAGGCTGAGGCAAGAGAATGGCAGAATGGCATGAACCCGGGAGGT CTGTAGGCCTAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCAGAATGGCATGAACCCGGGAGGT T C ARHGEF2 Ensembl:ENSG00000116584 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749716045 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57283 37225 RMVar_ID_37225 Human_SNP_ID_34843161 A-to-I Human chr1 - 155992405 155992405 155992405 GGGCATGGTGGCAGGCACCTGTAGGCCTAGCTACTCGGGAGGCTGAGGCAAGAGAATGGCAGAAT GGGCATGGTGGCAGGCACCTGTAGGCCTAGCTGCTCGGGAGGCTGAGGCAAGAGAATGGCAGAAT T C ARHGEF2 Ensembl:ENSG00000116584 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1441179984 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57283 37226 RMVar_ID_37226 Human_SNP_ID_34843928 A-to-I Human chr1 - 155995237 155995237 155995237 GTGGTGGCATGCACCTGTAGTCCTAGCTACTCAGGAGGCTAATGTGGGAGGATTGCTTGAGCCTG GTGGTGGCATGCACCTGTAGTCCTAGCTACTCCGGAGGCTAATGTGGGAGGATTGCTTGAGCCTG T G ARHGEF2 Ensembl:ENSG00000116584 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355959755 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57283 37227 RMVar_ID_37227 Human_SNP_ID_34848683 A-to-I Human chr1 - 156015255 156015255 156015255 CCAATCCACCCGCCTCGGCCTCCCAAAGTGCTAGGATTACAGGCGTGAGCCACCATGCCCGGCAA CCAATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCATGCCCGGCAA T C SSR2 Ensembl:ENSG00000163479 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1355382858 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3062,RMVar_hsa_circ_87891,RMVar_hsa_circ_136753,RMVar_hsa_circ_108462,RMVar_hsa_circ_284224,RMVar_hsa_circ_136757,RMVar_hsa_circ_136759 37228 RMVar_ID_37228 Human_SNP_ID_34848713 A-to-I Human chr1 - 156015363 156015363 156015363 AGCTGGGACTGCAGGCGCATGCTGCCATGCCCAGCTAATTTTTTCGTATTTTATTAGAGACGGGG AGCTGGGACTGCAGGCGCATGCTGCCATGCCCGGCTAATTTTTTCGTATTTTATTAGAGACGGGG T C SSR2 Ensembl:ENSG00000163479 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1234519812 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10604182 RMVar_hsa_circ_3062,RMVar_hsa_circ_87891,RMVar_hsa_circ_136753,RMVar_hsa_circ_108462,RMVar_hsa_circ_284224,RMVar_hsa_circ_136757,RMVar_hsa_circ_136759 37229 RMVar_ID_37229 Human_SNP_ID_34848963 A-to-I Human chr1 - 156015888 156015888 156015888 CTTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCTCCCATGCCTGGCCAAGTGACTATAAT CTTCGGCCTCCCAAAGTGCTGGGATTACAGGCCTGAGCTCCCATGCCTGGCCAAGTGACTATAAT T G SSR2 Ensembl:ENSG00000163479 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1242268015 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3062,RMVar_hsa_circ_87891,RMVar_hsa_circ_136753,RMVar_hsa_circ_108462,RMVar_hsa_circ_284224,RMVar_hsa_circ_136757,RMVar_hsa_circ_136759 37230 RMVar_ID_37230 Human_SNP_ID_34848998 A-to-I Human chr1 - 156016064 156016064 156016064 TCACTGCAACCTCTGGCTCCCGAGTTCAAGCGATTCTCCAGCCTCAGCCTCCAGAGTAGCTGGGA TCACTGCAACCTCTGGCTCCCGAGTTCAAGCGGTTCTCCAGCCTCAGCCTCCAGAGTAGCTGGGA T C SSR2 Ensembl:ENSG00000163479 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1340290116 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3062,RMVar_hsa_circ_87891,RMVar_hsa_circ_136753,RMVar_hsa_circ_108462,RMVar_hsa_circ_284224,RMVar_hsa_circ_136757,RMVar_hsa_circ_136759 37231 RMVar_ID_37231 Human_SNP_ID_34849016 A-to-I Human chr1 - 156016112 156016112 156016112 GTTTCGCTCTTGTCGCTCTTGTCTTGAGTGCAATGGTGCAATCTCGGCTCACTGCAACCTCTGGC GTTTCGCTCTTGTCGCTCTTGTCTTGAGTGCAGTGGTGCAATCTCGGCTCACTGCAACCTCTGGC T C SSR2 Ensembl:ENSG00000163479 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1470460853 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3062,RMVar_hsa_circ_87891,RMVar_hsa_circ_136753,RMVar_hsa_circ_108462,RMVar_hsa_circ_284224,RMVar_hsa_circ_136757,RMVar_hsa_circ_136759 37232 RMVar_ID_37232 Human_SNP_ID_34849080 A-to-I Human chr1 - 156016296 156016296 156016296 CCAGGAGGCGGAGCTTGCAGTGAGCTGAGATCATGCCACTGCACTTCAGCCTGGGCGACGGAGCG CCAGGAGGCGGAGCTTGCAGTGAGCTGAGATCGTGCCACTGCACTTCAGCCTGGGCGACGGAGCG T C SSR2 Ensembl:ENSG00000163479 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1010869576 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9459866 RMVar_hsa_circ_3062,RMVar_hsa_circ_87891,RMVar_hsa_circ_136753,RMVar_hsa_circ_108462,RMVar_hsa_circ_284224,RMVar_hsa_circ_136757,RMVar_hsa_circ_136759 37233 RMVar_ID_37233 Human_SNP_ID_34849115 A-to-I Human chr1 - 156016409 156016408 156016409 ACACACAGTGAAACCCTGTCTCTACTAAAAATACAAAAAAATTAGCCAGGCGTGGTGGCGGGCGC ACACACAGTGAAACCCTGTCTCTACTAAAAAT_CAAAAAAATTAGCCAGGCGTGGTGGCGGGCGC GT G SSR2 Ensembl:ENSG00000163479 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1430714061 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_3062,RMVar_hsa_circ_87891,RMVar_hsa_circ_136753,RMVar_hsa_circ_108462,RMVar_hsa_circ_284224,RMVar_hsa_circ_136757,RMVar_hsa_circ_136759 37234 RMVar_ID_37234 Human_SNP_ID_34849123 A-to-I Human chr1 - 156016435 156016434 156016436 TCAGGAGATCGAGACCATCCTGGCTAACACACAGTGAAACCCTGTCTCTACTAAAAATACAAAAA TCAGGAGATCGAGACCATCCTGGCTAACACA__GTGAAACCCTGTCTCTACTAAAAATACAAAAA CTG C SSR2 Ensembl:ENSG00000163479 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1431926066 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_3062,RMVar_hsa_circ_87891,RMVar_hsa_circ_136753,RMVar_hsa_circ_108462,RMVar_hsa_circ_284224,RMVar_hsa_circ_136757,RMVar_hsa_circ_136759 37235 RMVar_ID_37235 Human_SNP_ID_34849569 A-to-I Human chr1 - 156018016 156018016 156018016 AGCTGGGCACGGTGGCTCATGCCTGTAATCCCAGCATTTTTGGGAGGCCGAGGTGGGTGGATCAT AGCTGGGCACGGTGGCTCATGCCTGTAATCCCGGCATTTTTGGGAGGCCGAGGTGGGTGGATCAT T C SSR2 Ensembl:ENSG00000163479 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs933100613 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3062,RMVar_hsa_circ_87891,RMVar_hsa_circ_136753,RMVar_hsa_circ_108462,RMVar_hsa_circ_284224,RMVar_hsa_circ_136757,RMVar_hsa_circ_136759 37236 RMVar_ID_37236 Human_SNP_ID_34866538 A-to-I Human chr1 + 156085800 156085800 156085800 AGGTCTGGCAGGGCATGGTGGCTCGTTCCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGTGA AGGTCTGGCAGGGCATGGTGGCTCGTTCCTGTTATCCCAGCACTTTGGGAGGCCAAGGTGGGTGA A T LMNA Ensembl:ENSG00000160789 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs769152170 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114781,RMVar_hsa_circ_136770 37237 RMVar_ID_37237 Human_SNP_ID_34871915 A-to-I Human chr1 + 156110043 156110043 156110043 CTAATTTTTTTTTTAAGAGATGGGGTTTCACTATGTTGGCCAGGTTGGTCTTGAACTCCTGGGCT CTAATTTTTTTTTTAAGAGATGGGGTTTCACTCTGTTGGCCAGGTTGGTCTTGAACTCCTGGGCT A C LMNA Ensembl:ENSG00000160789 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277554304 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114781,RMVar_hsa_circ_136770 37238 RMVar_ID_37238 Human_SNP_ID_34872215 A-to-I Human chr1 + 156111399 156111399 156111399 TGAACCTGGGAGGCAGAGGTTGCAGTGAGCTGAGATTGTACTGTTGCACTTCAGCCTGGGTGACA TGAACCTGGGAGGCAGAGGTTGCAGTGAGCTGTGATTGTACTGTTGCACTTCAGCCTGGGTGACA A T LMNA Ensembl:ENSG00000160789 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928068044 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114781,RMVar_hsa_circ_136770 37239 RMVar_ID_37239 Human_SNP_ID_34874434 A-to-I Human chr1 + 156120550 156120550 156120550 CAGGAGTTTGAGACCAGTCTGGGCAACATAGCAAGACCCCCTTCTGTACAAAAAAATTAGCCGGT CAGGAGTTTGAGACCAGTCTGGGCAACATAGCGAGACCCCCTTCTGTACAAAAAAATTAGCCGGT A G LMNA Ensembl:ENSG00000160789 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs975766038 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114781,RMVar_hsa_circ_136770 37240 RMVar_ID_37240 Human_SNP_ID_34877758 A-to-I Human chr1 + 156134067 156134067 156134067 GAGACAGAGTCTAGCTGTGTCACCCAGGCTGGAGTGCAGTAGTGCGATCTCGGCTCACTGCAACC GAGACAGAGTCTAGCTGTGTCACCCAGGCTGGGGTGCAGTAGTGCGATCTCGGCTCACTGCAACC A G LMNA Ensembl:ENSG00000160789 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1243846125 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41174,RMVar_hsa_circ_114781,RMVar_hsa_circ_136770,RMVar_hsa_circ_103790,RMVar_hsa_circ_136773 37241 RMVar_ID_37241 Human_SNP_ID_34898424 A-to-I Human chr1 + 156214113 156214113 156214113 TTTTGTATCTGTACTAGTAGAGACGAGGTTTCACCATGTTGGCCAGGCTGGTCTGGAACTCCTGA TTTTGTATCTGTACTAGTAGAGACGAGGTTTCGCCATGTTGGCCAGGCTGGTCTGGAACTCCTGA A G PMF1-BGLAP,PMF1 Ensembl:ENSG00000260238,Ensembl:ENSG00000160783 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1003341361 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10604891 37242 RMVar_ID_37242 Human_SNP_ID_34898643 A-to-I Human chr1 + 156214908 156214908 156214908 TTATTATTATTTTTTTTTTTTAGGCAGTGTCTAGCTCTGTTGCCCAGGCTGGAGTGCAGTGGCTC TTATTATTATTTTTTTTTTTTAGGCAGTGTCTGGCTCTGTTGCCCAGGCTGGAGTGCAGTGGCTC A G PMF1-BGLAP,PMF1 Ensembl:ENSG00000260238,Ensembl:ENSG00000160783 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs998174735 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10604937,Human_RBP_ID_24594977 37243 RMVar_ID_37243 Human_SNP_ID_34899447 A-to-I Human chr1 + 156217632 156217632 156217632 CCAGTAATCTCAGCTACTTGGGAGGCTGAGGCAGGAGAATCACTTGAACCCAGGAGGCGGGGAAG CCAGTAATCTCAGCTACTTGGGAGGCTGAGGCGGGAGAATCACTTGAACCCAGGAGGCGGGGAAG A G PMF1-BGLAP,PMF1 Ensembl:ENSG00000260238,Ensembl:ENSG00000160783 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1208231056 Functional Loss SNV dbSNP153 33..33 33 - - - 37244 RMVar_ID_37244 Human_SNP_ID_34901162 A-to-I Human chr1 + 156224964 156224964 156224964 CTCTGTTGCCCAGGCTGGAGGGCAGTGGCGCCATCTTGGCTCACTGCAACCTCCGCCTCCCGGGT CTCTGTTGCCCAGGCTGGAGGGCAGTGGCGCCGTCTTGGCTCACTGCAACCTCCGCCTCCCGGGT A G PMF1-BGLAP,PMF1 Ensembl:ENSG00000260238,Ensembl:ENSG00000160783 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1347818166 Functional Loss SNV dbSNP153 33..33 33 - - - 37245 RMVar_ID_37245 Human_SNP_ID_34902791 A-to-I Human chr1 + 156231275 156231274 156231276 AGAATTAGCTGGTCATGATGGTGTGCACCTGTAGTCCTAGCTACTCAGGAGGCTGAGGCAAGAGG AGAATTAGCTGGTCATGATGGTGTGCACCTGT__TCCTAGCTACTCAGGAGGCTGAGGCAAGAGG TAG T PMF1-BGLAP,PMF1 Ensembl:ENSG00000260238,Ensembl:ENSG00000160783 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1207611263 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_50170 37246 RMVar_ID_37246 Human_SNP_ID_34909911 A-to-I Human chr1 - 156254990 156254990 156254990 GCTGTCCAGGTTCAAGCAGTTTTCCCTGCCTCAGCCTCCCAAGTAGCTGGGATTATAGGTGCCCG GCTGTCCAGGTTCAAGCAGTTTTCCCTGCCTCGGCCTCCCAAGTAGCTGGGATTATAGGTGCCCG T C SMG5 Ensembl:ENSG00000198952 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs191194966 Functional Loss SNV dbSNP153 33..33 33 - - - 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_136794 37247 RMVar_ID_37247 Human_SNP_ID_34910108 A-to-I Human chr1 - 156255787 156255787 156255787 GCAATTGTCCTGCCTCGGCCTCCTGAGTAGCTAGGACTACAGGCATGCATCACCAAGCTTGACTG GCAATTGTCCTGCCTCGGCCTCCTGAGTAGCTGGGACTACAGGCATGCATCACCAAGCTTGACTG T C SMG5 Ensembl:ENSG00000198952 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs115401208 Functional Loss SNV dbSNP153 33..33 33 - - - 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_136794 37248 RMVar_ID_37248 Human_SNP_ID_34910451 A-to-I Human chr1 - 156257043 156257043 156257043 AGGTGCCTGTAGTCCCAGCTACTTGGGAGGCTAAGGCAGAATAATCACTTGAACCTGGGAGGCAG AGGTGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGAATAATCACTTGAACCTGGGAGGCAG T C SMG5 Ensembl:ENSG00000198952 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1195837996 Functional Loss SNV dbSNP153 33..33 33 - - - 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_136794 37249 RMVar_ID_37249 Human_SNP_ID_34910763 A-to-I Human chr1 - 156258609 156258609 156258609 GTATTTTTAGTAGAGACAGGGTTTCACCATGTAGGCCAGGATGGTCTCGATCTCTTGCCCTTGTG GTATTTTTAGTAGAGACAGGGTTTCACCATGTGGGCCAGGATGGTCTCGATCTCTTGCCCTTGTG T C SMG5 Ensembl:ENSG00000198952 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs951719604 Functional Loss SNV dbSNP153 33..33 33 - - - 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_136794 37250 RMVar_ID_37250 Human_SNP_ID_34910771 A-to-I Human chr1 - 156258648 156258648 156258648 GGGACTACAGGCGCACGCCACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCA GGGACTACAGGCGCACGCCACCACGCCCAGCTGATTTTTGTATTTTTAGTAGAGACAGGGTTTCA T C SMG5 Ensembl:ENSG00000198952 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs552483651 Functional Loss SNV dbSNP153 33..33 33 - - - 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_136794 37251 RMVar_ID_37251 Human_SNP_ID_34913973 A-to-I Human chr1 - 156269563 156269563 156269563 CCTGGCTAATTTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTCATCTCGA CCTGGCTAATTTTTTGTATTTTTAGTAGAGACCGGGTTTCACCATGTTGGCCAGGCTCATCTCGA T G SMG5 Ensembl:ENSG00000198952 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1473070891 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34234,RMVar_hsa_circ_106487,RMVar_hsa_circ_96074,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_60394,RMVar_hsa_circ_80134,RMVar_hsa_circ_136795,RMVar_hsa_circ_112949,RMVar_hsa_circ_136798,RMVar_hsa_circ_136799,RMVar_hsa_circ_120492,RMVar_hsa_circ_366945 37252 RMVar_ID_37252 Human_SNP_ID_34919073 A-to-I Human chr1 + 156288413 156288413 156288413 GCTGGAGTGCAGTGGCGCAATCTTGGCTCACTACAACTTCTGTCTCCAGGCTCAAGCAGTTTTCC GCTGGAGTGCAGTGGCGCAATCTTGGCTCACTGCAACTTCTGTCTCCAGGCTCAAGCAGTTTTCC A G TMEM79 Ensembl:ENSG00000163472 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404424201 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136802,RMVar_hsa_circ_89278 37253 RMVar_ID_37253 Human_SNP_ID_34922760 A-to-I Human chr1 - 156300889 156300889 156300889 TCATTTCAGCCTCCGGAGAAGCTGGGACCACAAGCATGCACCACCATGCCCGGCTAATTTTTGTA TCATTTCAGCCTCCGGAGAAGCTGGGACCACAGGCATGCACCACCATGCCCGGCTAATTTTTGTA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1004729894 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10606830 37254 RMVar_ID_37254 Human_SNP_ID_34925234 A-to-I Human chr1 - 156309565 156309565 156309565 AAAATTAGCCAGGCATGGTGGTGCAGGCCTGTAATCCCAGCTGCTTGGGAGGCTGAGGTAGTAGA AAAATTAGCCAGGCATGGTGGTGCAGGCCTGTGATCCCAGCTGCTTGGGAGGCTGAGGTAGTAGA T C CCT3 Ensembl:ENSG00000163468 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1247990455 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123798,RMVar_hsa_circ_136809,RMVar_hsa_circ_91850,RMVar_hsa_circ_118445,RMVar_hsa_circ_136810,RMVar_hsa_circ_136811,RMVar_hsa_circ_136812 37255 RMVar_ID_37255 Human_SNP_ID_34928612 A-to-I Human chr1 - 156321828 156321824 156321828 TTTATTTTGGGGTTTTTTTGAGACGGAATCTCACTCTGTCACCCAGGCTGTCGTGCAGTGACATG TTTATTTTGGGGTTTTTTTGAGACGGAATCTC____TGTCACCCAGGCTGTCGTGCAGTGACATG AGAGT A CCT3 Ensembl:ENSG00000163468 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1055465523 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_10607420 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_136824 37256 RMVar_ID_37256 Human_SNP_ID_34928752 A-to-I Human chr1 - 156322411 156322411 156322411 CGGCTCACTGCAACCTCCGCCTCTTCGGTTCAAGCAATTCTGTCTCAGCCTCCCAAGTAGCTGGG CGGCTCACTGCAACCTCCGCCTCTTCGGTTCAGGCAATTCTGTCTCAGCCTCCCAAGTAGCTGGG T C CCT3 Ensembl:ENSG00000163468 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs987226686 Functional Loss SNV dbSNP153 33..33 33 - - - 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_136824 37257 RMVar_ID_37257 Human_SNP_ID_34928855 A-to-I Human chr1 - 156322747 156322747 156322747 TCAAGCAGTTTTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTATAGGCATGTGCCACTACGCCTG TCAAGCAGTTTTCCTGCCTCAGCCTCCCGAGTGGCTGGGATTATAGGCATGTGCCACTACGCCTG T C CCT3 Ensembl:ENSG00000163468 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1217023383 Functional Loss SNV dbSNP153 33..33 33 - - - 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_136824 37258 RMVar_ID_37258 Human_SNP_ID_34928870 A-to-I Human chr1 + 156322811 156322811 156322811 AAGCCAGGGAGCAGAGGTTGTAGTGAGCTGAGATCCAGCTATTGCATTCCAGCCTGAGCAACAAG AAGCCAGGGAGCAGAGGTTGTAGTGAGCTGAGGTCCAGCTATTGCATTCCAGCCTGAGCAACAAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs564884628 Functional Loss SNV dbSNP153 33..33 33 - - - 37259 RMVar_ID_37259 Human_SNP_ID_34929637 A-to-I Human chr1 - 156325514 156325510 156325514 TTTCATCATTTTATTTTTTGAGATAGGGTCTCACTCTGTCACCCAGATTGGAGTGCAATGGTGCG TTTCATCATTTTATTTTTTGAGATAGGGTCTC____TGTCACCCAGATTGGAGTGCAATGGTGCG AGAGT A CCT3 Ensembl:ENSG00000163468 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1487607926 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_136812,RMVar_hsa_circ_354013,RMVar_hsa_circ_136813,RMVar_hsa_circ_326160,RMVar_hsa_circ_136815,RMVar_hsa_circ_119918,RMVar_hsa_circ_290114,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_293454,RMVar_hsa_circ_63269,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 37260 RMVar_ID_37260 Human_SNP_ID_34929638 A-to-I Human chr1 - 156325514 156325514 156325514 TTTCATCATTTTATTTTTTGAGATAGGGTCTCACTCTGTCACCCAGATTGGAGTGCAATGGTGCG TTTCATCATTTTATTTTTTGAGATAGGGTCTCTCTCTGTCACCCAGATTGGAGTGCAATGGTGCG T A CCT3 Ensembl:ENSG00000163468 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1022189745 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136812,RMVar_hsa_circ_354013,RMVar_hsa_circ_136813,RMVar_hsa_circ_326160,RMVar_hsa_circ_136815,RMVar_hsa_circ_119918,RMVar_hsa_circ_290114,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_293454,RMVar_hsa_circ_63269,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 37261 RMVar_ID_37261 Human_SNP_ID_34930054 A-to-I Human chr1 - 156326851 156326851 156326851 GGTAGAGACAGTTTCACCATGTTGTCCAGGCTAGTCTCAAAACTCCTGGTCTCAAGCGATTTGCC GGTAGAGACAGTTTCACCATGTTGTCCAGGCTGGTCTCAAAACTCCTGGTCTCAAGCGATTTGCC T C CCT3 Ensembl:ENSG00000163468 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1202749971 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136812,RMVar_hsa_circ_354013,RMVar_hsa_circ_136813,RMVar_hsa_circ_326160,RMVar_hsa_circ_136815,RMVar_hsa_circ_119918,RMVar_hsa_circ_290114,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_293454,RMVar_hsa_circ_63269,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 37262 RMVar_ID_37262 Human_SNP_ID_34930061 A-to-I Human chr1 - 156326880 156326880 156326880 CAACACACCTGGCTAATTTTTGTATTTTTGGTAGAGACAGTTTCACCATGTTGTCCAGGCTAGTC CAACACACCTGGCTAATTTTTGTATTTTTGGTGGAGACAGTTTCACCATGTTGTCCAGGCTAGTC T C CCT3 Ensembl:ENSG00000163468 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs992426674 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10607494 RMVar_hsa_circ_136812,RMVar_hsa_circ_354013,RMVar_hsa_circ_136813,RMVar_hsa_circ_326160,RMVar_hsa_circ_136815,RMVar_hsa_circ_119918,RMVar_hsa_circ_290114,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_293454,RMVar_hsa_circ_63269,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 37263 RMVar_ID_37263 Human_SNP_ID_34930069 A-to-I Human chr1 - 156326924 156326924 156326924 CTTGTGCCTCAGCCTCCCAACTAGCTGGGATTACAGACACCCACCAACACACCTGGCTAATTTTT CTTGTGCCTCAGCCTCCCAACTAGCTGGGATTGCAGACACCCACCAACACACCTGGCTAATTTTT T C CCT3 Ensembl:ENSG00000163468 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs969596810 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136812,RMVar_hsa_circ_354013,RMVar_hsa_circ_136813,RMVar_hsa_circ_326160,RMVar_hsa_circ_136815,RMVar_hsa_circ_119918,RMVar_hsa_circ_290114,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_293454,RMVar_hsa_circ_63269,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 37264 RMVar_ID_37264 Human_SNP_ID_34931149 A-to-I Human chr1 - 156329682 156329682 156329682 CTCCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGACGTGAGCCACCATGCCCAGCCACTCAGC CTCCCACCTCAGCCTCCCAAAGTGCTGGGATTGCAGACGTGAGCCACCATGCCCAGCCACTCAGC T C CCT3 Ensembl:ENSG00000163468 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1252959455 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_136812,RMVar_hsa_circ_354013,RMVar_hsa_circ_136813,RMVar_hsa_circ_326160,RMVar_hsa_circ_136815,RMVar_hsa_circ_119918,RMVar_hsa_circ_290114,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_293454,RMVar_hsa_circ_63269,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 37265 RMVar_ID_37265 Human_SNP_ID_34931492 A-to-I Human chr1 - 156331047 156331047 156331047 TTATATTTTTAATAGTGACGGGATTTCACCATATTGGCCAGGCTGGTCTTGAACTCCTGACCTCA TTATATTTTTAATAGTGACGGGATTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGACCTCA T C CCT3 Ensembl:ENSG00000163468 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1161181919 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10607549 RMVar_hsa_circ_136812,RMVar_hsa_circ_354013,RMVar_hsa_circ_136813,RMVar_hsa_circ_326160,RMVar_hsa_circ_136815,RMVar_hsa_circ_119918,RMVar_hsa_circ_290114,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_293454,RMVar_hsa_circ_63269,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 37266 RMVar_ID_37266 Human_SNP_ID_34931752 A-to-I Human chr1 - 156331993 156331993 156331993 AGTCTCACTCTTGTTGCCCAGGCTGGAGTGCAATGGCACAATCTCGGCTCGCCGCAACCTCCCCC AGTCTCACTCTTGTTGCCCAGGCTGGAGTGCAGTGGCACAATCTCGGCTCGCCGCAACCTCCCCC T C CCT3 Ensembl:ENSG00000163468 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs544232954 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557347 RMVar_hsa_circ_136812,RMVar_hsa_circ_354013,RMVar_hsa_circ_136813,RMVar_hsa_circ_326160,RMVar_hsa_circ_136815,RMVar_hsa_circ_119918,RMVar_hsa_circ_290114,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_293454,RMVar_hsa_circ_63269,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 37267 RMVar_ID_37267 Human_SNP_ID_34934354 A-to-I Human chr1 + 156340947 156340947 156340947 TGTCTCCTTGATTCAAGTGATTCTTGTGCCTCAGCCACCCAAGTAGCTGGGATTACAGGTGTATG TGTCTCCTTGATTCAAGTGATTCTTGTGCCTCGGCCACCCAAGTAGCTGGGATTACAGGTGTATG A G TSACC Ensembl:ENSG00000163467 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1411015176 Functional Loss SNV dbSNP153 33..33 33 - - - 37268 RMVar_ID_37268 Human_SNP_ID_34951181 A-to-I Human chr1 - 156408781 156408781 156408781 GCCCGGCTAATTTTTGTAATTTTAGTAGAGACAGGGTTTTGCCATGTTGGCCAGGCTGGTCTCGA GCCCGGCTAATTTTTGTAATTTTAGTAGAGACGGGGTTTTGCCATGTTGGCCAGGCTGGTCTCGA T C C1orf61 Ensembl:ENSG00000125462 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1480066071 Functional Loss SNV dbSNP153 33..33 33 - - - 37269 RMVar_ID_37269 Human_SNP_ID_34951478 A-to-I Human chr1 - 156410041 156410041 156410041 CCAGCTATTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCTGGGAGGCAGAGGTTGCAGTGAGC CCAGCTATTCAGGAGGCTGAGGCAGGAGAATCTCTTGAACCTGGGAGGCAGAGGTTGCAGTGAGC T A C1orf61 Ensembl:ENSG00000125462 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs992640874 Functional Loss SNV dbSNP153 33..33 33 - - - 37270 RMVar_ID_37270 Human_SNP_ID_34951482 A-to-I Human chr1 - 156410063 156410063 156410063 ATGATGGCCCATGCCTGTAATCCCAGCTATTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCTG ATGATGGCCCATGCCTGTAATCCCAGCTATTCCGGAGGCTGAGGCAGGAGAATCACTTGAACCTG T G C1orf61 Ensembl:ENSG00000125462 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1459646222 Functional Loss SNV dbSNP153 33..33 33 - - - 37271 RMVar_ID_37271 Human_SNP_ID_34951483 A-to-I Human chr1 - 156410077 156410077 156410077 AAAATTAGCCAGGCATGATGGCCCATGCCTGTAATCCCAGCTATTCAGGAGGCTGAGGCAGGAGA AAAATTAGCCAGGCATGATGGCCCATGCCTGTCATCCCAGCTATTCAGGAGGCTGAGGCAGGAGA T G C1orf61 Ensembl:ENSG00000125462 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs923627463 Functional Loss SNV dbSNP153 33..33 33 - - - 37272 RMVar_ID_37272 Human_SNP_ID_34951487 A-to-I Human chr1 - 156410099 156410099 156410099 CCCTATCTCTACTAAAAATACAAAAATTAGCCAGGCATGATGGCCCATGCCTGTAATCCCAGCTA CCCTATCTCTACTAAAAATACAAAAATTAGCCGGGCATGATGGCCCATGCCTGTAATCCCAGCTA T C C1orf61 Ensembl:ENSG00000125462 Protein coding intron GSE47997;GSE107867 K562 cells&HepG2 cells;ASD brains,Fragile X samples from NIH NeuroBioBank - 23474544,30559470 RNA-Seq:(High) rs1239928094 Functional Loss SNV dbSNP153 33..33 33 - - - 37273 RMVar_ID_37273 Human_SNP_ID_34951491 A-to-I Human chr1 - 156410127 156410127 156410127 CAAGACCAGCCTGGCCAACATGGTGAAACCCTATCTCTACTAAAAATACAAAAATTAGCCAGGCA CAAGACCAGCCTGGCCAACATGGTGAAACCCTGTCTCTACTAAAAATACAAAAATTAGCCAGGCA T C C1orf61 Ensembl:ENSG00000125462 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1213573301 Functional Loss SNV dbSNP153 33..33 33 - - - 37274 RMVar_ID_37274 Human_SNP_ID_34951492 A-to-I Human chr1 - 156410133 156410133 156410133 GGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCCTATCTCTACTAAAAATACAAAAATTAGC GGAGTTCAAGACCAGCCTGGCCAACATGGTGAGACCCTATCTCTACTAAAAATACAAAAATTAGC T C C1orf61 Ensembl:ENSG00000125462 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1048647409 Functional Loss SNV dbSNP153 33..33 33 - - - 37275 RMVar_ID_37275 Human_SNP_ID_34951507 A-to-I Human chr1 - 156410185 156410185 156410185 CCTGTAATCTCAGCACTTTGGGAGGCCAAGGCAGGTGGATCGCCTGAGGTCAGGAGTTCAAGACC CCTGTAATCTCAGCACTTTGGGAGGCCAAGGCGGGTGGATCGCCTGAGGTCAGGAGTTCAAGACC T C C1orf61 Ensembl:ENSG00000125462 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1416924203 Functional Loss SNV dbSNP153 33..33 33 - - - 37276 RMVar_ID_37276 Human_SNP_ID_34951515 A-to-I Human chr1 - 156410203 156410203 156410203 CGGGCGCAGTGGCCCAAGCCTGTAATCTCAGCACTTTGGGAGGCCAAGGCAGGTGGATCGCCTGA CGGGCGCAGTGGCCCAAGCCTGTAATCTCAGCGCTTTGGGAGGCCAAGGCAGGTGGATCGCCTGA T C C1orf61 Ensembl:ENSG00000125462 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1235025764 Functional Loss SNV dbSNP153 33..33 33 - - - 37277 RMVar_ID_37277 Human_SNP_ID_34951516 A-to-I Human chr1 - 156410203 156410203 156410203 CGGGCGCAGTGGCCCAAGCCTGTAATCTCAGCACTTTGGGAGGCCAAGGCAGGTGGATCGCCTGA CGGGCGCAGTGGCCCAAGCCTGTAATCTCAGCCCTTTGGGAGGCCAAGGCAGGTGGATCGCCTGA T G C1orf61 Ensembl:ENSG00000125462 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1235025764 Functional Loss SNV dbSNP153 33..33 33 - - - 37278 RMVar_ID_37278 Human_SNP_ID_34951941 A-to-I Human chr1 - 156411822 156411822 156411822 TCACCCAGGCTGGAGTGCAGTGGCGCAATCTCAGCTCACTGCAACCTCTGCCGCCCGGGTTCAAG TCACCCAGGCTGGAGTGCAGTGGCGCAATCTCGGCTCACTGCAACCTCTGCCGCCCGGGTTCAAG T C C1orf61 Ensembl:ENSG00000125462 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1207857775 Functional Loss SNV dbSNP153 33..33 33 - - - 37279 RMVar_ID_37279 Human_SNP_ID_34952205 A-to-I Human chr1 - 156412783 156412783 156412783 GGCTGAGGCTTCAGAAAGAAAGAGGCAGGGGTAGGAGGCAAGGCTGTGGGAACGGAAGCGGAGGG GGCTGAGGCTTCAGAAAGAAAGAGGCAGGGGTGGGAGGCAAGGCTGTGGGAACGGAAGCGGAGGG T C C1orf61 Ensembl:ENSG00000125462 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1383961476 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5312718 37280 RMVar_ID_37280 Human_SNP_ID_34966617 A-to-I Human chr1 - 156469842 156469842 156469842 AGACAAGATCCCACAGGCTGGAGTGCAGTGGCATGATCATAGCTCACTGCAGCCTCAACCTCCCA AGACAAGATCCCACAGGCTGGAGTGCAGTGGCGTGATCATAGCTCACTGCAGCCTCAACCTCCCA T C MEF2D Ensembl:ENSG00000116604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs960945473 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28877,RMVar_hsa_circ_100777,RMVar_hsa_circ_136846 37281 RMVar_ID_37281 Human_SNP_ID_34966720 A-to-I Human chr1 - 156470256 156470256 156470256 CGCCACCGCCTGGCTAATTTTTTGTATTTTTAATAGAGATGGGGTTTCACCATGTTGGCCAGGCT CGCCACCGCCTGGCTAATTTTTTGTATTTTTATTAGAGATGGGGTTTCACCATGTTGGCCAGGCT T A MEF2D Ensembl:ENSG00000116604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1392839833 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28877,RMVar_hsa_circ_100777,RMVar_hsa_circ_136846 37282 RMVar_ID_37282 Human_SNP_ID_34966973 A-to-I Human chr1 - 156471271 156471271 156471271 CAAAAATTAGCTGGGCGTGATGGTGTGCGCCTATAATCCCAGCTACTCGGGAAGCTGAGGTAGGA CAAAAATTAGCTGGGCGTGATGGTGTGCGCCTGTAATCCCAGCTACTCGGGAAGCTGAGGTAGGA T C MEF2D Ensembl:ENSG00000116604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1199344347 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24595721 RMVar_hsa_circ_28877,RMVar_hsa_circ_100777,RMVar_hsa_circ_136846 37283 RMVar_ID_37283 Human_SNP_ID_34967324 A-to-I Human chr1 - 156472838 156472838 156472838 GGATGTAGTGGCATGTGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAA GGATGTAGTGGCATGTGCCTGTAATCCCAGCTGCTCGGGAGGCTGAGGCAGGAGAATCACTTGAA T C MEF2D Ensembl:ENSG00000116604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1310212156 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28877,RMVar_hsa_circ_100777,RMVar_hsa_circ_136846 37284 RMVar_ID_37284 Human_SNP_ID_34967333 A-to-I Human chr1 - 156472911 156472911 156472911 GGTCAGGAGATCGAGACCATCCTGGCTAACACAGTGAAACCCTGTCTCTACTAAAAATACAGAAA GGTCAGGAGATCGAGACCATCCTGGCTAACACCGTGAAACCCTGTCTCTACTAAAAATACAGAAA T G MEF2D Ensembl:ENSG00000116604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs891757281 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28877,RMVar_hsa_circ_100777,RMVar_hsa_circ_136846 37285 RMVar_ID_37285 Human_SNP_ID_34967655 A-to-I Human chr1 - 156474266 156474266 156474266 TTTTGTATCTTTAGTAGAGATAGGTTTTTGCCATGTTGCCTGGGCTGGTCTCAAACTCCTGAGTT TTTTGTATCTTTAGTAGAGATAGGTTTTTGCCGTGTTGCCTGGGCTGGTCTCAAACTCCTGAGTT T C MEF2D Ensembl:ENSG00000116604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1176167899 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24595729 RMVar_hsa_circ_28877,RMVar_hsa_circ_100777,RMVar_hsa_circ_136846 37286 RMVar_ID_37286 Human_SNP_ID_34967673 A-to-I Human chr1 - 156474349 156474349 156474349 TTCTTCCTGGGTTCAGGTGATTCTCATGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCATGCG TTCTTCCTGGGTTCAGGTGATTCTCATGCCTCTGCCTCCTGAGTAGCTGGGATTACAGGCATGCG T A MEF2D Ensembl:ENSG00000116604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs902173914 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28877,RMVar_hsa_circ_100777,RMVar_hsa_circ_136846 37287 RMVar_ID_37287 Human_SNP_ID_34967674 A-to-I Human chr1 - 156474349 156474349 156474349 TTCTTCCTGGGTTCAGGTGATTCTCATGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCATGCG TTCTTCCTGGGTTCAGGTGATTCTCATGCCTCGGCCTCCTGAGTAGCTGGGATTACAGGCATGCG T C MEF2D Ensembl:ENSG00000116604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs902173914 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28877,RMVar_hsa_circ_100777,RMVar_hsa_circ_136846 37288 RMVar_ID_37288 Human_SNP_ID_34967772 A-to-I Human chr1 - 156474750 156474750 156474750 ACTGGAGTACAGTGGTGCCATCCTAGCTCACTACAGCCTTGAACTCCTGGGCTCAAGTGATCCTC ACTGGAGTACAGTGGTGCCATCCTAGCTCACTGCAGCCTTGAACTCCTGGGCTCAAGTGATCCTC T C MEF2D Ensembl:ENSG00000116604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1009621539 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28877,RMVar_hsa_circ_100777,RMVar_hsa_circ_136846 37289 RMVar_ID_37289 Human_SNP_ID_34967780 A-to-I Human chr1 - 156474774 156474774 156474774 ACAGGGTTTCACTCTGTCACCCAGACTGGAGTACAGTGGTGCCATCCTAGCTCACTACAGCCTTG ACAGGGTTTCACTCTGTCACCCAGACTGGAGTCCAGTGGTGCCATCCTAGCTCACTACAGCCTTG T G MEF2D Ensembl:ENSG00000116604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1366526350 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28877,RMVar_hsa_circ_100777,RMVar_hsa_circ_136846 37290 RMVar_ID_37290 Human_SNP_ID_34967784 A-to-I Human chr1 - 156474796 156474796 156474796 TGTTTTTTTTTTCTTTTTTGGAACAGGGTTTCACTCTGTCACCCAGACTGGAGTACAGTGGTGCC TGTTTTTTTTTTCTTTTTTGGAACAGGGTTTCGCTCTGTCACCCAGACTGGAGTACAGTGGTGCC T C MEF2D Ensembl:ENSG00000116604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1003405233 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28877,RMVar_hsa_circ_100777,RMVar_hsa_circ_136846 37291 RMVar_ID_37291 Human_SNP_ID_35013361 A-to-I Human chr1 - 156649683 156649682 156649683 AGATATGGGCAGGTTTGGGTGCAGTGGCTCACACCTATAAATCCCAGCACTTCGGGAGTCCAAGA AGATATGGGCAGGTTTGGGTGCAGTGGCTCAC_CCTATAAATCCCAGCACTTCGGGAGTCCAAGA GT G AL590666.2 Ensembl:ENSG00000229953 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1468538503 Functional Loss DEL dbSNP153 33..33 33 - - - 37292 RMVar_ID_37292 Human_SNP_ID_35030418 A-to-I Human chr1 - 156713166 156713166 156713166 GTTGGTCAGGCTGGTCTCGAACTCCCGACCTCAGATGATCCACCCCCTTCGGCCTCCCAAAGTGC GTTGGTCAGGCTGGTCTCGAACTCCCGACCTCTGATGATCCACCCCCTTCGGCCTCCCAAAGTGC T A AL590666.1 Ensembl:ENSG00000223356 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1356254191 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10609118 37293 RMVar_ID_37293 Human_SNP_ID_35030571 A-to-I Human chr1 - 156713601 156713601 156713601 TCAAGCGATTCTCCTCCCTCAGCCTCCTGAGTAGCTGGGGTTACAGGCACACATCATCACGTTCA TCAAGCGATTCTCCTCCCTCAGCCTCCTGAGTGGCTGGGGTTACAGGCACACATCATCACGTTCA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1269219081 Functional Loss SNV dbSNP153 33..33 33 - - - 37294 RMVar_ID_37294 Human_SNP_ID_35033137 A-to-I Human chr1 - 156723268 156723268 156723268 AGAAACAGGGCAGTGGACCAATGGACAGCTCCACCAGCTCCACATCTTTGGAAGCTAGATTTGGG AGAAACAGGGCAGTGGACCAATGGACAGCTCCGCCAGCTCCACATCTTTGGAAGCTAGATTTGGG T C ISG20L2 Ensembl:ENSG00000143319 Protein coding exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs765513040 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_328984,Human_RBP_ID_5697445,Human_RBP_ID_10609412,Human_RBP_ID_17212922,Human_RBP_ID_17446695,Human_RBP_ID_17727529,Human_RBP_ID_27169695 Human_miRNA_ID_270694 37295 RMVar_ID_37295 Human_SNP_ID_35035199 A-to-I Human chr1 + 156730605 156730605 156730605 AAATAAAAAAATAGCTAGGCTTGGCAGCACACACCTGTAGTCCCAGCTACTAGGGAGGCTGAGGC AAATAAAAAAATAGCTAGGCTTGGCAGCACACCCCTGTAGTCCCAGCTACTAGGGAGGCTGAGGC A C RRNAD1 Ensembl:ENSG00000143303 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs920453681 Functional Loss SNV dbSNP153 33..33 33 - - - 37296 RMVar_ID_37296 Human_SNP_ID_35038252 A-to-I Human chr1 - 156740996 156740996 156740996 GCCCGTCCGAGAGGCAGGTGCGGGAAGAGCCTATCCTTTTCCCTGGCCATGGCTCAGTCGCCTCC GCCCGTCCGAGAGGCAGGTGCGGGAAGAGCCTGTCCTTTTCCCTGGCCATGGCTCAGTCGCCTCC T C MRPL24 Ensembl:ENSG00000143314 Protein coding intron GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs1237039456 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23121518 Human_Splice_Rec_143589 RMVar_hsa_circ_127038,RMVar_hsa_circ_136897 37297 RMVar_ID_37297 Human_SNP_ID_35038806 A-to-I Human chr1 - 156743062 156743062 156743062 GCATTCTGGACCTCTGGGTTGGGATCAGGGGTAGGAATGGAAAGGATGGAGCATCAACAGCAGGG GCATTCTGGACCTCTGGGTTGGGATCAGGGGTGGGAATGGAAAGGATGGAGCATCAACAGCAGGG T C HDGF Ensembl:ENSG00000143321 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1273904177 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_329062,Human_RBP_ID_971817,Human_RBP_ID_1150027,Human_RBP_ID_1413598,Human_RBP_ID_1727096,Human_RBP_ID_2097223,Human_RBP_ID_3283289,Human_RBP_ID_5312730,Human_RBP_ID_5697590,Human_RBP_ID_8169694,Human_RBP_ID_8287606,Human_RBP_ID_9352527,Human_RBP_ID_10609744,Human_RBP_ID_17330744,Human_RBP_ID_17446723,Human_RBP_ID_17727587,Human_RBP_ID_18217795,Human_RBP_ID_18428737,Human_RBP_ID_18553626,Human_RBP_ID_19203015,Human_RBP_ID_23121521,Human_RBP_ID_23336942,Human_RBP_ID_26386568,Human_RBP_ID_26844121,Human_RBP_ID_27152859,Human_RBP_ID_27169766,Human_RBP_ID_27389569 Human_miRNA_ID_1187891 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 37298 RMVar_ID_37298 Human_SNP_ID_35042031 A-to-I Human chr1 + 156754175 156754175 156754175 TGACCTTGTCATCCACCTGCCTTGGCCTCCCAAAGTGCTGGGATTATAGGCGTGAGCAACCGCGC TGACCTTGTCATCCACCTGCCTTGGCCTCCCACAGTGCTGGGATTATAGGCGTGAGCAACCGCGC A C PRCC Ensembl:ENSG00000143294 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs938264310 Functional Loss SNV dbSNP153 33..33 33 - - - 37299 RMVar_ID_37299 Human_SNP_ID_35050984 A-to-I Human chr1 + 156787971 156787971 156787971 CTCCCACCTCAGCCTCCCAAATAGCTGGGACTACAGGCACATTCCACCATGCCCGCTAATTTAAT CTCCCACCTCAGCCTCCCAAATAGCTGGGACTGCAGGCACATTCCACCATGCCCGCTAATTTAAT A G PRCC Ensembl:ENSG00000143294 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1171209651 Functional Loss SNV dbSNP153 33..33 33 - - - 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 37300 RMVar_ID_37300 Human_SNP_ID_35051226 A-to-I Human chr1 + 156788940 156788940 156788940 TGCCCACCTGGGCCTCCCAAAGTGCTGGGGTTACAGAGGTGAGCTACCGCGCCCTGCCTATTTTT TGCCCACCTGGGCCTCCCAAAGTGCTGGGGTTGCAGAGGTGAGCTACCGCGCCCTGCCTATTTTT A G PRCC Ensembl:ENSG00000143294 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs573251484 Functional Loss SNV dbSNP153 33..33 33 - - - 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 37301 RMVar_ID_37301 Human_SNP_ID_35051582 A-to-I Human chr1 + 156790502 156790501 156790502 AAAATTAGCTGAGCGTGCTGGCATGCGCCTGTAATCCCAGCTACGTGGAAGGCTGAGACAGGAGA AAAATTAGCTGAGCGTGCTGGCATGCGCCTGT_ATCCCAGCTACGTGGAAGGCTGAGACAGGAGA TA T PRCC Ensembl:ENSG00000143294 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1185968045 Functional Loss DEL dbSNP153 33..33 33 - - - 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 37302 RMVar_ID_37302 Human_SNP_ID_35051598 A-to-I Human chr1 + 156790548 156790548 156790548 GGAAGGCTGAGACAGGAGAATCGCTTGAACCCAGGAGGCGAGGTTGCAGTGAGCCAAGATGGCGC GGAAGGCTGAGACAGGAGAATCGCTTGAACCCGGGAGGCGAGGTTGCAGTGAGCCAAGATGGCGC A G PRCC Ensembl:ENSG00000143294 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs573413645 Functional Loss SNV dbSNP153 33..33 33 - - - 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 37303 RMVar_ID_37303 Human_SNP_ID_35115368 A-to-I Human chr1 - 157029404 157029404 157029404 AGCTGGGCATGGTGGTAGGTGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGAGGCAGGAGAATTG AGCTGGGCATGGTGGTAGGTGCCTGTAGTCCCTGCTACTCAGGAGGCTGAGAGGCAGGAGAATTG T A ARHGEF11 Ensembl:ENSG00000132694 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs972829907 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127797,RMVar_hsa_circ_136946 37304 RMVar_ID_37304 Human_SNP_ID_35122629 A-to-I Human chr1 - 157059876 157059876 157059876 AATCAAGGTATGGAAGATTCAGAGTAGACAATATTTAAGGAGATATGAGAGGGCACACAGTAAGG AATCAAGGTATGGAAGATTCAGAGTAGACAATGTTTAAGGAGATATGAGAGGGCACACAGTAAGG T C SMU1P1 Ensembl:ENSG00000237842 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878931799 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5245021 37305 RMVar_ID_37305 Human_SNP_ID_35122632 A-to-I Human chr1 - 157059883 157059883 157059883 ATGGAAAAATCAAGGTATGGAAGATTCAGAGTAGACAATATTTAAGGAGATATGAGAGGGCACAC ATGGAAAAATCAAGGTATGGAAGATTCAGAGTGGACAATATTTAAGGAGATATGAGAGGGCACAC T C SMU1P1 Ensembl:ENSG00000237842 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879200614 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5245021 Human_miRNA_ID_1911881 37306 RMVar_ID_37306 Human_SNP_ID_35122635 A-to-I Human chr1 - 157059899 157059899 157059899 GCAACTGGGGCCCAAGATGGAAAAATCAAGGTATGGAAGATTCAGAGTAGACAATATTTAAGGAG GCAACTGGGGCCCAAGATGGAAAAATCAAGGTGTGGAAGATTCAGAGTAGACAATATTTAAGGAG T C SMU1P1 Ensembl:ENSG00000237842 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878988658 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5245021,Human_RBP_ID_8242766,Human_RBP_ID_17340405,Human_RBP_ID_18523597 Human_miRNA_ID_1911881 37307 RMVar_ID_37307 Human_SNP_ID_35138233 A-to-I Human chr1 - 157122855 157122855 157122855 CTACCTTTCCCCAGGAATGGGACTGAGAGGGTAGTCTCCAGCAACTCAGTCTGCACAGGGCTCCC CTACCTTTCCCCAGGAATGGGACTGAGAGGGTGGTCTCCAGCAACTCAGTCTGCACAGGGCTCCC T C ETV3 Ensembl:ENSG00000117036 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1329910585 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_329194,Human_RBP_ID_5698246,Human_RBP_ID_22780766 37308 RMVar_ID_37308 Human_SNP_ID_35284491 A-to-I Human chr1 + 157709274 157709274 157709274 TCTTCTGAACAAGGCAGACCATCCAAACGTCTAACAGATTTGGATAAGGCTCAATTACTTGAAAT TCTTCTGAACAAGGCAGACCATCCAAACGTCTGACAGATTTGGATAAGGCTCAATTACTTGAAAT A G AL356276.2 Ensembl:ENSG00000231700 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1456952264 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1413718,Human_RBP_ID_5091478,Human_RBP_ID_5889751,Human_RBP_ID_8241404,Human_RBP_ID_8735976,Human_RBP_ID_18217859,Human_RBP_ID_18553753,Human_RBP_ID_22376291,Human_RBP_ID_26844242 37309 RMVar_ID_37309 Human_SNP_ID_35284566 A-to-I Human chr1 - 157709614 157709614 157709614 TTCTTTTGTTAAGGTTACCTGGCTTTTTGGTGAAGCTGGTTTTGCTGCAGCAATATTCAGATTGA TTCTTTTGTTAAGGTTACCTGGCTTTTTGGTGGAGCTGGTTTTGCTGCAGCAATATTCAGATTGA T C lnc-FCRL3-2 RNACentral:URS00008B3ECD lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1418474733 Functional Loss SNV dbSNP153 33..33 33 - - - 37310 RMVar_ID_37310 Human_SNP_ID_35310130 A-to-I Human chr1 - 157809299 157809299 157809299 CTCCCACCTCAGCCTTCCAAAGTGTTGGGATTACAGTCATAAGCCACTGCATCTGGCTTGGATCT CTCCCACCTCAGCCTTCCAAAGTGTTGGGATTGCAGTCATAAGCCACTGCATCTGGCTTGGATCT T C FCRL1 Ensembl:ENSG00000163534 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1405479175 Functional Loss SNV dbSNP153 33..33 33 - - - 37311 RMVar_ID_37311 Human_SNP_ID_35310293 A-to-I Human chr1 - 157809886 157809886 157809886 AGGGTCTTACTCTGTTGCCCCAGCTGAAGTGCAGTGGTATGGTCATGGCTCATTGCAACCTTGAA AGGGTCTTACTCTGTTGCCCCAGCTGAAGTGCGGTGGTATGGTCATGGCTCATTGCAACCTTGAA T C FCRL1 Ensembl:ENSG00000163534 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs551295326 Functional Loss SNV dbSNP153 33..33 33 - - - 37312 RMVar_ID_37312 Human_SNP_ID_35310295 A-to-I Human chr1 - 157809892 157809892 157809892 AGAGTCAGGGTCTTACTCTGTTGCCCCAGCTGAAGTGCAGTGGTATGGTCATGGCTCATTGCAAC AGAGTCAGGGTCTTACTCTGTTGCCCCAGCTGTAGTGCAGTGGTATGGTCATGGCTCATTGCAAC T A FCRL1 Ensembl:ENSG00000163534 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs113912926 Functional Loss SNV dbSNP153 33..33 33 - - - 37313 RMVar_ID_37313 Human_SNP_ID_35310296 A-to-I Human chr1 - 157809892 157809892 157809892 AGAGTCAGGGTCTTACTCTGTTGCCCCAGCTGAAGTGCAGTGGTATGGTCATGGCTCATTGCAAC AGAGTCAGGGTCTTACTCTGTTGCCCCAGCTGCAGTGCAGTGGTATGGTCATGGCTCATTGCAAC T G FCRL1 Ensembl:ENSG00000163534 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs113912926 Functional Loss SNV dbSNP153 33..33 33 - - - 37314 RMVar_ID_37314 Human_SNP_ID_35310423 A-to-I Human chr1 - 157810372 157810372 157810372 GAATTGCATGAACTTGTGAGGTAGAGGTTGCAATGAGCCAAGATCATGCCACTGCATTCCAGCCT GAATTGCATGAACTTGTGAGGTAGAGGTTGCAGTGAGCCAAGATCATGCCACTGCATTCCAGCCT T C FCRL1 Ensembl:ENSG00000163534 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs935342542 Functional Loss SNV dbSNP153 33..33 33 - - - 37315 RMVar_ID_37315 Human_SNP_ID_35310424 A-to-I Human chr1 - 157810373 157810373 157810373 AGAATTGCATGAACTTGTGAGGTAGAGGTTGCAATGAGCCAAGATCATGCCACTGCATTCCAGCC AGAATTGCATGAACTTGTGAGGTAGAGGTTGCGATGAGCCAAGATCATGCCACTGCATTCCAGCC T C FCRL1 Ensembl:ENSG00000163534 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1464884794 Functional Loss SNV dbSNP153 33..33 33 - - - 37316 RMVar_ID_37316 Human_SNP_ID_35478607 A-to-I Human chr1 + 158455037 158455037 158455037 TCATAGCAATGCAGTCCTCATATACTATCAGCAGCTGCCTTTTCTCTATCCTCTTTCCTTTATTC TCATAGCAATGCAGTCCTCATATACTATCAGCGGCTGCCTTTTCTCTATCCTCTTTCCTTTATTC A G EI24P2 Ensembl:ENSG00000236257 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs570959178 Functional Loss SNV dbSNP153 33..33 33 - - - 37317 RMVar_ID_37317 Human_SNP_ID_35635130 A-to-I Human chr1 + 159051087 159051087 159051087 TTTTATTTTATTTGGTCACTGTCATATTAGGCAGGAGGGAACTTTTCTTTAACCTCCTCTCTCCA TTTTATTTTATTTGGTCACTGTCATATTAGGCGGGAGGGAACTTTTCTTTAACCTCCTCTCTCCA A G IFI16 Ensembl:ENSG00000163565 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1434005381 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37680 37318 RMVar_ID_37318 Human_SNP_ID_35885222 A-to-I Human chr1 - 160026800 160026800 160026800 TTTTTCTGAGACAAGATGTTGCTTTGTCACCCAGGCTGGAGTGCAGTAGTATAAACATGGCTCAC TTTTTCTGAGACAAGATGTTGCTTTGTCACCCCGGCTGGAGTGCAGTAGTATAAACATGGCTCAC T G PIGM,KCNJ10 Ensembl:ENSG00000143315,Ensembl:ENSG00000177807 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1173106827 Functional Loss SNV dbSNP153 33..33 33 - - - 37319 RMVar_ID_37319 Human_SNP_ID_35885285 A-to-I Human chr1 - 160027089 160027089 160027089 TTTAAGAGCTGGGCATGGTGGTTCATGCCTATAATCCCAATGCTTTGGGAAGCTGAGGCAGGAGG TTTAAGAGCTGGGCATGGTGGTTCATGCCTATGATCCCAATGCTTTGGGAAGCTGAGGCAGGAGG T C PIGM,KCNJ10 Ensembl:ENSG00000143315,Ensembl:ENSG00000177807 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1199396643 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10613539 37320 RMVar_ID_37320 Human_SNP_ID_35914353 A-to-I Human chr1 + 160142662 160142662 160142662 CCTGTCTCTACTAAAAGTACAAAAAATTAGCCAGTCATGGTGGCACACGCCTGTAATCTCAGCTA CCTGTCTCTACTAAAAGTACAAAAAATTAGCCGGTCATGGTGGCACACGCCTGTAATCTCAGCTA A G ATP1A2 Ensembl:ENSG00000018625 Protein coding 3'UTR GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1393011262 Functional Loss SNV dbSNP153 33..33 33 - - - 37321 RMVar_ID_37321 Human_SNP_ID_35933461 A-to-I Human chr1 + 160214294 160214294 160214294 GAGGTTGAAGAATGAGACCCTTAGGTTTTAACACGAATCCTGACACCACCATCTATAGGGTCCCA GAGGTTGAAGAATGAGACCCTTAGGTTTTAACGCGAATCCTGACACCACCATCTATAGGGTCCCA A G PEA15 Ensembl:ENSG00000162734 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1248154436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1345091,Human_RBP_ID_1413823,Human_RBP_ID_8957029,Human_RBP_ID_10613788,Human_RBP_ID_26370130 RMVar_hsa_circ_82603,RMVar_hsa_circ_127021,RMVar_hsa_circ_136996,RMVar_hsa_circ_136998 37322 RMVar_ID_37322 Human_SNP_ID_35936792 A-to-I Human chr1 - 160229825 160229825 160229825 TAGAACCGAGGTCTCACCGTGTTAGCCAGGCTAGTCTCGAACTCCTGACCTCAGGTGATCTGCCC TAGAACCGAGGTCTCACCGTGTTAGCCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCTGCCC T C DCAF8,AL139011.2 Ensembl:ENSG00000132716,Ensembl:ENSG00000258465 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984067048 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10614322 RMVar_hsa_circ_93317,RMVar_hsa_circ_123319,RMVar_hsa_circ_74628,RMVar_hsa_circ_137003,RMVar_hsa_circ_137004,RMVar_hsa_circ_346799,RMVar_hsa_circ_109951,RMVar_hsa_circ_137005,RMVar_hsa_circ_115602,RMVar_hsa_circ_342229,RMVar_hsa_circ_342606,RMVar_hsa_circ_267279,RMVar_hsa_circ_52929,RMVar_hsa_circ_137010,RMVar_hsa_circ_137008,RMVar_hsa_circ_137009,RMVar_hsa_circ_125505,RMVar_hsa_circ_340875,RMVar_hsa_circ_348906 37323 RMVar_ID_37323 Human_SNP_ID_35943632 A-to-I Human chr1 - 160257869 160257869 160257869 AAAAAAAAGCCAAGCATGGGGCAAGTACTTGCAGTCCCATCTCCTTGGGAGGCTGAGGTGGGAGG AAAAAAAAGCCAAGCATGGGGCAAGTACTTGCGGTCCCATCTCCTTGGGAGGCTGAGGTGGGAGG T C DCAF8,AL139011.2 Ensembl:ENSG00000132716,Ensembl:ENSG00000258465 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1218816223 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557363 RMVar_hsa_circ_346799,RMVar_hsa_circ_115602,RMVar_hsa_circ_342606,RMVar_hsa_circ_137009,RMVar_hsa_circ_348906,RMVar_hsa_circ_299355,RMVar_hsa_circ_344533,RMVar_hsa_circ_137016 37324 RMVar_ID_37324 Human_SNP_ID_35943638 A-to-I Human chr1 - 160257889 160257889 160257889 TTGTCTCTACAAAAAGTTTAAAAAAAAAGCCAAGCATGGGGCAAGTACTTGCAGTCCCATCTCCT TTGTCTCTACAAAAAGTTTAAAAAAAAAGCCAGGCATGGGGCAAGTACTTGCAGTCCCATCTCCT T C DCAF8,AL139011.2 Ensembl:ENSG00000132716,Ensembl:ENSG00000258465 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs983137489 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557363 RMVar_hsa_circ_346799,RMVar_hsa_circ_115602,RMVar_hsa_circ_342606,RMVar_hsa_circ_137009,RMVar_hsa_circ_348906,RMVar_hsa_circ_299355,RMVar_hsa_circ_344533,RMVar_hsa_circ_137016 37325 RMVar_ID_37325 Human_SNP_ID_35943649 A-to-I Human chr1 - 160257937 160257937 160257937 ATCACTTGATCCTAGTTGTTCAAGTCCAGCCTAGGCAATATTGAGACCTTGTCTCTACAAAAAGT ATCACTTGATCCTAGTTGTTCAAGTCCAGCCTGGGCAATATTGAGACCTTGTCTCTACAAAAAGT T C DCAF8,AL139011.2 Ensembl:ENSG00000132716,Ensembl:ENSG00000258465 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1486951186 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17558472 RMVar_hsa_circ_346799,RMVar_hsa_circ_115602,RMVar_hsa_circ_342606,RMVar_hsa_circ_137009,RMVar_hsa_circ_348906,RMVar_hsa_circ_299355,RMVar_hsa_circ_344533,RMVar_hsa_circ_137016 37326 RMVar_ID_37326 Human_SNP_ID_35943650 A-to-I Human chr1 - 160257948 160257948 160257948 AAGGTGGGAGGATCACTTGATCCTAGTTGTTCAAGTCCAGCCTAGGCAATATTGAGACCTTGTCT AAGGTGGGAGGATCACTTGATCCTAGTTGTTCGAGTCCAGCCTAGGCAATATTGAGACCTTGTCT T C DCAF8,AL139011.2 Ensembl:ENSG00000132716,Ensembl:ENSG00000258465 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs560289430 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557364 RMVar_hsa_circ_346799,RMVar_hsa_circ_115602,RMVar_hsa_circ_342606,RMVar_hsa_circ_137009,RMVar_hsa_circ_348906,RMVar_hsa_circ_299355,RMVar_hsa_circ_344533,RMVar_hsa_circ_137016 37327 RMVar_ID_37327 Human_SNP_ID_35943663 A-to-I Human chr1 - 160258002 160258002 160258002 GCCAGGCTGAGTGCGGCTGGCTCATGGCTGTAATCCCAGCACTTTTGGGAGGCCAAGGTGGGAGG GCCAGGCTGAGTGCGGCTGGCTCATGGCTGTAGTCCCAGCACTTTTGGGAGGCCAAGGTGGGAGG T C DCAF8,AL139011.2 Ensembl:ENSG00000132716,Ensembl:ENSG00000258465 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs532759384 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_346799,RMVar_hsa_circ_115602,RMVar_hsa_circ_342606,RMVar_hsa_circ_137009,RMVar_hsa_circ_348906,RMVar_hsa_circ_299355,RMVar_hsa_circ_344533,RMVar_hsa_circ_137016 37328 RMVar_ID_37328 Human_SNP_ID_35945687 A-to-I Human chr1 - 160266143 160266143 160266143 TCATCCAGGCTGGAGTGCAGTGGTGTGACCTCAGTTCACTGCAACCTCTGCCTCCCAGGCTCAAG TCATCCAGGCTGGAGTGCAGTGGTGTGACCTCGGTTCACTGCAACCTCTGCCTCCCAGGCTCAAG T C AL139011.2 Ensembl:ENSG00000258465 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs931136113 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115602,RMVar_hsa_circ_137009 37329 RMVar_ID_37329 Human_SNP_ID_35948968 A-to-I Human chr1 - 160279179 160279179 160279179 CTTTACGTCCAGGGTCTTTGTGCCTTGTCTCTACTCCCTCTCTTGGATCTGGGGAGGAGGGGCAG CTTTACGTCCAGGGTCTTTGTGCCTTGTCTCTGCTCCCTCTCTTGGATCTGGGGAGGAGGGGCAG T C PEX19,AL139011.2 Ensembl:ENSG00000162735,Ensembl:ENSG00000258465 Protein coding,Protein coding 3'UTR,intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1224084695 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_329804,Human_RBP_ID_2097766,Human_RBP_ID_17728135,Human_RBP_ID_19445520,Human_RBP_ID_26370238 Human_miRNA_ID_1219340 RMVar_hsa_circ_115602,RMVar_hsa_circ_137009 37330 RMVar_ID_37330 Human_SNP_ID_35951800 A-to-I Human chr1 - 160289651 160289641 160289651 AGGAGGTGGAGGTTGCATTCAACTGAGATCATACCACTTCATTCCAGCCTGGGTGACAGAGCAAG AGGAGGTGGAGGTTGCATTCAACTGAGATCAT__________TCCAGCCTGGGTGACAGAGCAAG AATGAAGTGGT A COPA Ensembl:ENSG00000122218 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1557858405 Functional Loss DEL dbSNP153 33..42 33 - - - Human_RBP_ID_8957067,Human_RBP_ID_18553988,Human_RBP_ID_24597333 RMVar_hsa_circ_103491,RMVar_hsa_circ_137019,RMVar_hsa_circ_99830,RMVar_hsa_circ_137018 37331 RMVar_ID_37331 Human_SNP_ID_35954785 A-to-I Human chr1 - 160302757 160302757 160302757 GAGGTCAGGAGATCGAGACCATCCTGGCTAACACGGTGAAACCCCATCTCTACTAAAAATACAAA GAGGTCAGGAGATCGAGACCATCCTGGCTAACGCGGTGAAACCCCATCTCTACTAAAAATACAAA T C COPA Ensembl:ENSG00000122218 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs866710675 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_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 37332 RMVar_ID_37332 Human_SNP_ID_35954842 A-to-I Human chr1 - 160302943 160302943 160302943 GTCTCGAACTCCTGACCTCAAGCCATCCTCCCACATCAGCTTCCCAAAGTGCTGGGATTGCAGGC GTCTCGAACTCCTGACCTCAAGCCATCCTCCCCCATCAGCTTCCCAAAGTGCTGGGATTGCAGGC T G COPA Ensembl:ENSG00000122218 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1347641641 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5125308,Human_RBP_ID_22469501 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_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_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 37333 RMVar_ID_37333 Human_SNP_ID_35954856 A-to-I Human chr1 - 160302990 160302990 160302990 ACTTGTATTTTGAGTAGAGATGGGGTTTCACCATATTGGCCAGGCTGGTCTCGAACTCCTGACCT ACTTGTATTTTGAGTAGAGATGGGGTTTCACCGTATTGGCCAGGCTGGTCTCGAACTCCTGACCT T C COPA Ensembl:ENSG00000122218 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs896704101 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_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 37334 RMVar_ID_37334 Human_SNP_ID_35958332 A-to-I Human chr1 - 160317584 160317584 160317584 AGCAATTCTCTGACCCTCAAAGAGAAACCTGAATGAATTCATTGGAACGCCCTGTCTTTGACAGT AGCAATTCTCTGACCCTCAAAGAGAAACCTGAGTGAATTCATTGGAACGCCCTGTCTTTGACAGT T C COPA Ensembl:ENSG00000122218 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879101280 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10616068 RMVar_hsa_circ_99830,RMVar_hsa_circ_137018,RMVar_hsa_circ_4835,RMVar_hsa_circ_109880,RMVar_hsa_circ_137027,RMVar_hsa_circ_137028,RMVar_hsa_circ_97323,RMVar_hsa_circ_71098,RMVar_hsa_circ_86396,RMVar_hsa_circ_88577,RMVar_hsa_circ_137036,RMVar_hsa_circ_326348,RMVar_hsa_circ_137038,RMVar_hsa_circ_137039,RMVar_hsa_circ_329218,RMVar_hsa_circ_375472,RMVar_hsa_circ_77953,RMVar_hsa_circ_137043,RMVar_hsa_circ_137044,RMVar_hsa_circ_137042,RMVar_hsa_circ_119249,RMVar_hsa_circ_137049,RMVar_hsa_circ_372695,RMVar_hsa_circ_137053,RMVar_hsa_circ_121007,RMVar_hsa_circ_137052,RMVar_hsa_circ_97844,RMVar_hsa_circ_353959,RMVar_hsa_circ_328339,RMVar_hsa_circ_38219,RMVar_hsa_circ_137070,RMVar_hsa_circ_81166,RMVar_hsa_circ_120443,RMVar_hsa_circ_126411,RMVar_hsa_circ_137054,RMVar_hsa_circ_119141,RMVar_hsa_circ_108976,RMVar_hsa_circ_137056,RMVar_hsa_circ_45880,RMVar_hsa_circ_84740,RMVar_hsa_circ_137058,RMVar_hsa_circ_137059,RMVar_hsa_circ_137057,RMVar_hsa_circ_332104,RMVar_hsa_circ_137055,RMVar_hsa_circ_336028,RMVar_hsa_circ_90612,RMVar_hsa_circ_137066,RMVar_hsa_circ_137067,RMVar_hsa_circ_137068,RMVar_hsa_circ_137065,RMVar_hsa_circ_82993,RMVar_hsa_circ_313808,RMVar_hsa_circ_137069,RMVar_hsa_circ_345145,RMVar_hsa_circ_137071 37335 RMVar_ID_37335 Human_SNP_ID_35965122 A-to-I Human chr1 + 160345772 160345772 160345772 ATCTGCCAGCATGGTGAAACCCCCCCATCTCTACTAAAAATACAAAAATTAGCCGGCTGGCTGCT ATCTGCCAGCATGGTGAAACCCCCCCATCTCTCCTAAAAATACAAAAATTAGCCGGCTGGCTGCT A C NCSTN Ensembl:ENSG00000162736 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs975320368 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108205,RMVar_hsa_circ_137081,RMVar_hsa_circ_137080,RMVar_hsa_circ_371672 37336 RMVar_ID_37336 Human_SNP_ID_36054963 A-to-I Human chr1 - 160704403 160704403 160704403 CACACACAAGAGTTTGCAACCCTCATACATGTATCCCGCTAACCCCAACTAAGTACTTCCCATTT CACACACAAGAGTTTGCAACCCTCATACATGTGTCCCGCTAACCCCAACTAAGTACTTCCCATTT T C CD48 Ensembl:ENSG00000117091 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs185084835 Functional Loss SNV dbSNP153 33..33 33 - - - 37337 RMVar_ID_37337 Human_SNP_ID_36054966 A-to-I Human chr1 - 160704409 160704409 160704409 GAACTTCACACACAAGAGTTTGCAACCCTCATACATGTATCCCGCTAACCCCAACTAAGTACTTC GAACTTCACACACAAGAGTTTGCAACCCTCATGCATGTATCCCGCTAACCCCAACTAAGTACTTC T C CD48 Ensembl:ENSG00000117091 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1408278822 Functional Loss SNV dbSNP153 33..33 33 - - - 37338 RMVar_ID_37338 Human_SNP_ID_36055206 A-to-I Human chr1 - 160705485 160705485 160705485 CCATTTTACAAAACATATCTTAAACATTAATTAGACCACAGCCTCTGTCTTCTCTAACATCCCCT CCATTTTACAAAACATATCTTAAACATTAATTGGACCACAGCCTCTGTCTTCTCTAACATCCCCT T C CD48 Ensembl:ENSG00000117091 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1337255609 Functional Loss SNV dbSNP153 33..33 33 - - - 37339 RMVar_ID_37339 Human_SNP_ID_36082989 A-to-I Human chr1 + 160815083 160815083 160815083 GACTAGGAGGCCAGGTGCGGTGGCTCACACCTATAATCCCGGTACTTTGGGAGGCTGAGGCAGGT GACTAGGAGGCCAGGTGCGGTGGCTCACACCTGTAATCCCGGTACTTTGGGAGGCTGAGGCAGGT A G LY9 Ensembl:ENSG00000122224 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs917536226 Functional Loss SNV dbSNP153 33..33 33 - - - 37340 RMVar_ID_37340 Human_SNP_ID_36083041 A-to-I Human chr1 + 160815296 160815296 160815296 CCAAGGGGCGGAGGTTTCAGTGAGCCGAGATCATGCCACTTCACTCCAGCCTGAGAGAAAGAGCA CCAAGGGGCGGAGGTTTCAGTGAGCCGAGATCGTGCCACTTCACTCCAGCCTGAGAGAAAGAGCA A G LY9 Ensembl:ENSG00000122224 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs543702537 Functional Loss SNV dbSNP153 33..33 33 - - - 37341 RMVar_ID_37341 Human_SNP_ID_36083092 A-to-I Human chr1 + 160815456 160815456 160815456 TCACCCAGGCTGGAGTACAGTGGCACGATCTCAGCTCACTGCAACCTCTGACTACCAAGTTCAAG TCACCCAGGCTGGAGTACAGTGGCACGATCTCGGCTCACTGCAACCTCTGACTACCAAGTTCAAG A G LY9 Ensembl:ENSG00000122224 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs765810334 Functional Loss SNV dbSNP153 33..33 33 - - - 37342 RMVar_ID_37342 Human_SNP_ID_36103695 A-to-I Human chr1 + 160895764 160895764 160895764 CTAATAGAAGACTGTATCCCGGTACTGAAGAGATACACCAAAGAAGGGAGAGAATTTGATTATGT CTAATAGAAGACTGTATCCCGGTACTGAAGAGGTACACCAAAGAAGGGAGAGAATTTGATTATGT A G AL354714.2 Ensembl:ENSG00000213080 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878870680 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1911248 37343 RMVar_ID_37343 Human_SNP_ID_36130078 A-to-I Human chr1 - 160995031 160995031 160995031 CTCAGCTCACTGCAACTTCTCCCTCTGAGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGCAGC CTCAGCTCACTGCAACTTCTCCCTCTGAGTTCTAGCGATTCTCCTGCCTCAGCCTCCCGAGCAGC T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1182032157 Functional Loss SNV dbSNP153 33..33 33 - - - 37344 RMVar_ID_37344 Human_SNP_ID_36130247 A-to-I Human chr1 - 160995589 160995589 160995589 TGCCACCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGA TGCCACCATGCCCAGCTAATTTTTGTATTTTTGGTAGAGACGGGGTTTCACCATGTTGGCCAGGA T C F11R Ensembl:ENSG00000158769 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1402526502 Functional Loss SNV dbSNP153 33..33 33 - - - 37345 RMVar_ID_37345 Human_SNP_ID_36130261 A-to-I Human chr1 - 160995665 160995665 160995665 TCACTGCAACCTCCACCTCCTGGGTTCAAGCAATTCTCTTGCCTCAGCCTCCTAAGTAGCTGGGA TCACTGCAACCTCCACCTCCTGGGTTCAAGCAGTTCTCTTGCCTCAGCCTCCTAAGTAGCTGGGA T C F11R Ensembl:ENSG00000158769 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs761676923 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_627018 37346 RMVar_ID_37346 Human_SNP_ID_36130439 A-to-I Human chr1 - 160996425 160996425 160996425 GTTCTGTGTCATGGTTGGAAGACAGAGTAGGAAGGATATGGAAAAGGTCATGGGGAAGCAGAGGT GTTCTGTGTCATGGTTGGAAGACAGAGTAGGAGGGATATGGAAAAGGTCATGGGGAAGCAGAGGT T C F11R Ensembl:ENSG00000158769 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1365802864 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5700003,Human_RBP_ID_17675429,Human_RBP_ID_17764183,Human_RBP_ID_23338379,Human_RBP_ID_26386614 Human_miRNA_ID_1056252,Human_miRNA_ID_1187896,Human_miRNA_ID_1473555 37347 RMVar_ID_37347 Human_SNP_ID_36130458 A-to-I Human chr1 - 160996511 160996511 160996511 CGCCTGCCTTGGCCTCCCAAAGTGATGGGATTACAGATGTGAGCCACCGTGCCTAGCCAAGGATG CGCCTGCCTTGGCCTCCCAAAGTGATGGGATTGCAGATGTGAGCCACCGTGCCTAGCCAAGGATG T C F11R Ensembl:ENSG00000158769 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1352851877 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_330018,Human_RBP_ID_4002232,Human_RBP_ID_5641849,Human_RBP_ID_5700010,Human_RBP_ID_22369307,Human_RBP_ID_22560530,Human_RBP_ID_23338379,Human_RBP_ID_26386616,Human_RBP_ID_27390044 37348 RMVar_ID_37348 Human_SNP_ID_36130468 A-to-I Human chr1 - 160996563 160996563 160996563 CAGGGTTTCACCATGTTGGTCGGGCTGGTCTCAAACTCCTGACCTCTTGATCCGCCTGCCTTGGC CAGGGTTTCACCATGTTGGTCGGGCTGGTCTCGAACTCCTGACCTCTTGATCCGCCTGCCTTGGC T C F11R Ensembl:ENSG00000158769 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE99789;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;ASD brains,Fragile X samples from NIH NeuroBioBank;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,29129909,29796672,30559470,31158229,31158229,32596459 RNA-Seq:(High) rs1158918574 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5641849,Human_RBP_ID_22369307,Human_RBP_ID_26386618 37349 RMVar_ID_37349 Human_SNP_ID_36130488 A-to-I Human chr1 - 160996644 160996644 160996644 CTCCTGCCTCAGTCTCCTGAGTAGCTGGGATTACGGGTGCGTGCCACCATGCCTGGCTAATTTTT CTCCTGCCTCAGTCTCCTGAGTAGCTGGGATTGCGGGTGCGTGCCACCATGCCTGGCTAATTTTT T C F11R Ensembl:ENSG00000158769 Protein coding 3'UTR GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,29796672,31158229,31158229,31158229 RNA-Seq:(High) rs879209469 Functional Loss SNV dbSNP153 33..33 33 - - - 37350 RMVar_ID_37350 Human_SNP_ID_36130559 A-to-I Human chr1 - 160996942 160996942 160996942 GGAAATCCCTAACAGAATTGAGTTTTCTATTAAGGATCCAAAAAGAAAAACAAAATGCTAATGAA GGAAATCCCTAACAGAATTGAGTTTTCTATTACGGATCCAAAAAGAAAAACAAAATGCTAATGAA T G F11R Ensembl:ENSG00000158769 Protein coding 3'UTR GSE100210;GSE112787 HepG2 cell line;293 Flip-In T-REx cells,empty vector - 29129909,29967493 RNA-Seq:(High) rs989557071 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_330020,Human_RBP_ID_17728261 Human_miRNA_ID_1056254,Human_miRNA_ID_1473557 37351 RMVar_ID_37351 Human_SNP_ID_36130800 A-to-I Human chr1 - 160998043 160998043 160998043 ACCCTACTAAAAATACAAAGTTAGCCAGGCATAGTGGTGCATGCCTGTAATCCCAGCTGCTCAGG ACCCTACTAAAAATACAAAGTTAGCCAGGCATGGTGGTGCATGCCTGTAATCCCAGCTGCTCAGG T C F11R,AL591806.4 Ensembl:ENSG00000158769,Ensembl:ENSG00000270149 Protein coding,Protein coding 3'UTR,3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs11624 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4002259,Human_RBP_ID_17728265,Human_RBP_ID_26386633 37352 RMVar_ID_37352 Human_SNP_ID_36130802 A-to-I Human chr1 - 160998058 160998056 160998058 GACCAACATGGAGAAACCCTACTAAAAATACAAAGTTAGCCAGGCATAGTGGTGCATGCCTGTAA GACCAACATGGAGAAACCCTACTAAAAATACA__GTTAGCCAGGCATAGTGGTGCATGCCTGTAA CTT C F11R,AL591806.4 Ensembl:ENSG00000158769,Ensembl:ENSG00000270149 Protein coding,Protein coding 3'UTR,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1032403510 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_4002260,Human_RBP_ID_17728265,Human_RBP_ID_26370340 37353 RMVar_ID_37353 Human_SNP_ID_36130806 A-to-I Human chr1 - 160998067 160998067 160998067 GATCAGCCTGACCAACATGGAGAAACCCTACTAAAAATACAAAGTTAGCCAGGCATAGTGGTGCA GATCAGCCTGACCAACATGGAGAAACCCTACTGAAAATACAAAGTTAGCCAGGCATAGTGGTGCA T C F11R,AL591806.4 Ensembl:ENSG00000158769,Ensembl:ENSG00000270149 Protein coding,Protein coding 3'UTR,3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1127862 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17728265,Human_RBP_ID_26370340 37354 RMVar_ID_37354 Human_SNP_ID_36130814 A-to-I Human chr1 - 160998100 160998100 160998100 AGGCAGGCGGATCACCTGAGGTCAGGAGTTCAAGATCAGCCTGACCAACATGGAGAAACCCTACT AGGCAGGCGGATCACCTGAGGTCAGGAGTTCAGGATCAGCCTGACCAACATGGAGAAACCCTACT T C F11R,AL591806.4 Ensembl:ENSG00000158769,Ensembl:ENSG00000270149 Protein coding,Protein coding 3'UTR,3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1127860 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4002262,Human_RBP_ID_26388790 Human_miRNA_ID_1538201,Human_miRNA_ID_1538202,Human_miRNA_ID_1592600,Human_miRNA_ID_1592601,Human_miRNA_ID_1688288,Human_miRNA_ID_1688289 37355 RMVar_ID_37355 Human_SNP_ID_36130823 A-to-I Human chr1 - 160998148 160998148 160998148 AAACTGGAGGCTGGGCGCAGTGGCTCACGCCTATAATCCCAGAGGCTGAGGCAGGCGGATCACCT AAACTGGAGGCTGGGCGCAGTGGCTCACGCCTGTAATCCCAGAGGCTGAGGCAGGCGGATCACCT T C F11R,AL591806.4 Ensembl:ENSG00000158769,Ensembl:ENSG00000270149 Protein coding,Protein coding 3'UTR,3'UTR GSE38233;GSE100210;GSE112787;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;293 Flip-In T-REx cells,empty vector;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,29967493,31158229,32596459 RNA-Seq:(High) rs879041811 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8169714,Human_RBP_ID_26386635 37356 RMVar_ID_37356 Human_SNP_ID_36132516 A-to-I Human chr1 - 161004218 161004218 161004218 TATATGGCCAGGCGTGATGGTTCACATCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGAGAA TATATGGCCAGGCGTGATGGTTCACATCTGTAGTCCCAGCACTTTGGGAGGCCAAGGCAGGAGAA T C F11R,AL591806.4 Ensembl:ENSG00000158769,Ensembl:ENSG00000270149 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs775091984 Functional Loss SNV dbSNP153 33..33 33 - - - 37357 RMVar_ID_37357 Human_SNP_ID_36133846 A-to-I Human chr1 - 161009750 161009750 161009750 TTGGCCCGGCTGGTCTTAAACTTCTGACCTCAAGCAATCCACCCACATCGGCCTCCCAAAGTGCT TTGGCCCGGCTGGTCTTAAACTTCTGACCTCATGCAATCCACCCACATCGGCCTCCCAAAGTGCT T A F11R,AL591806.4 Ensembl:ENSG00000158769,Ensembl:ENSG00000270149 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1479583530 Functional Loss SNV dbSNP153 33..33 33 - - - 37358 RMVar_ID_37358 Human_SNP_ID_36137155 A-to-I Human chr1 - 161022638 161022638 161022638 TGTATTTAGTAGAGACAGGGTTTCACCACGTTAGTCAGACTGACCTCAGGTGATCCACCCACCTC TGTATTTAGTAGAGACAGGGTTTCACCACGTTTGTCAGACTGACCTCAGGTGATCCACCCACCTC T A AL591806.4 Ensembl:ENSG00000270149 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1344282558 Functional Loss SNV dbSNP153 33..33 33 - - - 37359 RMVar_ID_37359 Human_SNP_ID_36137701 A-to-I Human chr1 - 161024568 161024568 161024568 GAGGTCGGGAGTTCGAGACCAGCCTGACCAACATGGAAAAACCCCGCGTACTAAAAATACAAAAT GAGGTCGGGAGTTCGAGACCAGCCTGACCAACGTGGAAAAACCCCGCGTACTAAAAATACAAAAT T C AL591806.4 Ensembl:ENSG00000270149 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs549491056 Functional Loss SNV dbSNP153 33..33 33 - - - 37360 RMVar_ID_37360 Human_SNP_ID_36137702 A-to-I Human chr1 - 161024568 161024568 161024568 GAGGTCGGGAGTTCGAGACCAGCCTGACCAACATGGAAAAACCCCGCGTACTAAAAATACAAAAT GAGGTCGGGAGTTCGAGACCAGCCTGACCAACCTGGAAAAACCCCGCGTACTAAAAATACAAAAT T G AL591806.4 Ensembl:ENSG00000270149 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs549491056 Functional Loss SNV dbSNP153 33..33 33 - - - 37361 RMVar_ID_37361 Human_SNP_ID_36138514 A-to-I Human chr1 - 161027904 161027904 161027904 TTGGGAGGCCGAGGCAGGTGGATCACGAGGTCAGGAGATCGAGACTATCCTGGACAACATGGTGA TTGGGAGGCCGAGGCAGGTGGATCACGAGGTCGGGAGATCGAGACTATCCTGGACAACATGGTGA T C AL591806.4 Ensembl:ENSG00000270149 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs907650962 Functional Loss SNV dbSNP153 33..33 33 - - - 37362 RMVar_ID_37362 Human_SNP_ID_36138749 A-to-I Human chr1 - 161028803 161028803 161028803 TCAAGTGATTCTCCTGCTTCAGCCTCTCGAGTAGCTGGGACTCCAGGCACTTGCCACAATGCCCA TCAAGTGATTCTCCTGCTTCAGCCTCTCGAGTGGCTGGGACTCCAGGCACTTGCCACAATGCCCA T C AL591806.4 Ensembl:ENSG00000270149 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1044640536 Functional Loss SNV dbSNP153 33..33 33 - - - 37363 RMVar_ID_37363 Human_SNP_ID_36140159 A-to-I Human chr1 - 161033725 161033723 161033725 GATTATGCACTGCACTCCAGTTTGTGTGACAGAGTGAGACCCTGTCTCAAAAAAAAAAAAAAAAA GATTATGCACTGCACTCCAGTTTGTGTGACAG__TGAGACCCTGTCTCAAAAAAAAAAAAAAAAA ACT A AL591806.4 Ensembl:ENSG00000270149 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1310190893 Functional Loss DEL dbSNP153 33..34 33 - - - 37364 RMVar_ID_37364 Human_SNP_ID_36140435 A-to-I Human chr1 - 161034772 161034772 161034772 TTGCCCAGGCTGGAGTGCAATGGGGCGATCTCAGCTCACTGCAACCTCTGCCTCCGGGGTTCAAG TTGCCCAGGCTGGAGTGCAATGGGGCGATCTCGGCTCACTGCAACCTCTGCCTCCGGGGTTCAAG T C AL591806.4 Ensembl:ENSG00000270149 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1409554139 Functional Loss SNV dbSNP153 33..33 33 - - - 37365 RMVar_ID_37365 Human_SNP_ID_36141848 A-to-I Human chr1 - 161039747 161039747 161039747 CCCTGTGATATGGCGGCCTGCAGTGGTGTGAAACACACAATGTGGACGTGCACTGACAGCCTTGC CCCTGTGATATGGCGGCCTGCAGTGGTGTGAAGCACACAATGTGGACGTGCACTGACAGCCTTGC T C USF1 Ensembl:ENSG00000158773 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1486656536 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_330063,Human_RBP_ID_10617517,Human_RBP_ID_26799093,Human_RBP_ID_27170289 37366 RMVar_ID_37366 Human_SNP_ID_36147672 A-to-I Human chr1 - 161057556 161057556 161057556 ATGGCTCACTGCAGCCTCTACCTCCTAGGCTCAAGCGATCCTCCTACCTCAGCCTTCTGAGTAGT ATGGCTCACTGCAGCCTCTACCTCCTAGGCTCTAGCGATCCTCCTACCTCAGCCTTCTGAGTAGT T A ARHGAP30 Ensembl:ENSG00000186517 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1240915123 Functional Loss SNV dbSNP153 33..33 33 - - - 37367 RMVar_ID_37367 Human_SNP_ID_36147821 A-to-I Human chr1 - 161058190 161058190 161058190 CTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCACATGTCACCACTCCCGGTTAATTTTT CTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTCCAGGCACATGTCACCACTCCCGGTTAATTTTT T G ARHGAP30 Ensembl:ENSG00000186517 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs999278292 Functional Loss SNV dbSNP153 33..33 33 - - - 37368 RMVar_ID_37368 Human_SNP_ID_36147835 A-to-I Human chr1 - 161058226 161058226 161058226 CTCACTGCAGCCTCTGACTCCTAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGG CTCACTGCAGCCTCTGACTCCTAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGG T C ARHGAP30 Ensembl:ENSG00000186517 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1244186953 Functional Loss SNV dbSNP153 33..33 33 - - - 37369 RMVar_ID_37369 Human_SNP_ID_36148144 A-to-I Human chr1 - 161059301 161059301 161059301 ACTTGAGCCAGGCGCGGTGGCTCACGCTTGTAATCTCAGCACTCTGGGAGGCTGAAGTGGGTGGA ACTTGAGCCAGGCGCGGTGGCTCACGCTTGTAGTCTCAGCACTCTGGGAGGCTGAAGTGGGTGGA T C ARHGAP30 Ensembl:ENSG00000186517 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1475848294 Functional Loss SNV dbSNP153 33..33 33 - - - 37370 RMVar_ID_37370 Human_SNP_ID_36148469 A-to-I Human chr1 - 161060514 161060514 161060514 TCAGCTCACTGAAACCTCCACCTCCTGGTTCAAGTGATTCTCTTGCCTCAGCCTCCCAAGTAGCT TCAGCTCACTGAAACCTCCACCTCCTGGTTCAGGTGATTCTCTTGCCTCAGCCTCCCAAGTAGCT T C ARHGAP30 Ensembl:ENSG00000186517 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1259935076 Functional Loss SNV dbSNP153 33..33 33 - - - 37371 RMVar_ID_37371 Human_SNP_ID_36149022 A-to-I Human chr1 - 161062617 161062615 161062618 TCAAGCAATTCTTCTGCCTCAGCCACCCAAGTAGCTGGGACTACAGACACATGCCACCACATCAG TCAAGCAATTCTTCTGCCTCAGCCACCCAAG___CTGGGACTACAGACACATGCCACCACATCAG GCTA G ARHGAP30 Ensembl:ENSG00000186517 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs146313130 Functional Loss DEL dbSNP153 32..34 33 - - - 37372 RMVar_ID_37372 Human_SNP_ID_36149035 A-to-I Human chr1 - 161062677 161062677 161062677 TCCCCCAGGCTGGAGTGCAGTGGTGCAATCTCAGCTCACTGCAACAACTACCTCCCAGATTCAAG TCCCCCAGGCTGGAGTGCAGTGGTGCAATCTCGGCTCACTGCAACAACTACCTCCCAGATTCAAG T C ARHGAP30 Ensembl:ENSG00000186517 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs28531878 Functional Loss SNV dbSNP153 33..33 33 - - - 37373 RMVar_ID_37373 Human_SNP_ID_36149529 A-to-I Human chr1 - 161064634 161064634 161064634 CCTGCTTTAGCCTCCTGAGTAGCTGGGACTACAGGTGTGAGCCACCATGCCCTGCTAATTTTTTG CCTGCTTTAGCCTCCTGAGTAGCTGGGACTACGGGTGTGAGCCACCATGCCCTGCTAATTTTTTG T C ARHGAP30 Ensembl:ENSG00000186517 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1326558692 Functional Loss SNV dbSNP153 33..33 33 - - - 37374 RMVar_ID_37374 Human_SNP_ID_36150085 A-to-I Human chr1 - 161065704 161065704 161065704 AAATTAGCCGGGCAGAGTGGTGGGTGCCTGTAATCCTAGCTACTTGGGAGGCTGAGGCAGGAGAA AAATTAGCCGGGCAGAGTGGTGGGTGCCTGTAGTCCTAGCTACTTGGGAGGCTGAGGCAGGAGAA T C ARHGAP30 Ensembl:ENSG00000186517 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs993193169 Functional Loss SNV dbSNP153 33..33 33 - - - 37375 RMVar_ID_37375 Human_SNP_ID_36150095 A-to-I Human chr1 - 161065749 161065749 161065749 CAGCCTGACCAACATGGAGAAACTCTGTCTCTACTAGAAATATAAAAATTAGCCGGGCAGAGTGG CAGCCTGACCAACATGGAGAAACTCTGTCTCTCCTAGAAATATAAAAATTAGCCGGGCAGAGTGG T G ARHGAP30 Ensembl:ENSG00000186517 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs775834687 Functional Loss SNV dbSNP153 33..33 33 - - - 37376 RMVar_ID_37376 Human_SNP_ID_36150315 A-to-I Human chr1 - 161066522 161066522 161066522 TCCCTGCCTCAGCCTCTCGAGTAGCTGGGACTACAGGCACCACCACGCCTGGCTAATTTTTGTAC TCCCTGCCTCAGCCTCTCGAGTAGCTGGGACTGCAGGCACCACCACGCCTGGCTAATTTTTGTAC T C ARHGAP30 Ensembl:ENSG00000186517 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1205106041 Functional Loss SNV dbSNP153 33..33 33 - - - 37377 RMVar_ID_37377 Human_SNP_ID_36161331 A-to-I Human chr1 - 161109365 161109365 161109365 AAATTATTTAAGTAACTAATATGCATTTTTATATGAGCACATATAAAGGGTTAACATATGGGAAT AAATTATTTAAGTAACTAATATGCATTTTTATGTGAGCACATATAAAGGGTTAACATATGGGAAT T C PFDN2 Ensembl:ENSG00000143256 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4656985 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_110 GWAS_ID_4085,GWAS_ID_4086,GWAS_ID_4087,GWAS_ID_4088,GWAS_ID_4089,GWAS_ID_4090,GWAS_ID_4091,GWAS_ID_4092,GWAS_ID_4093,GWAS_ID_4094,GWAS_ID_4095,GWAS_ID_4096,GWAS_ID_4097,GWAS_ID_4098,GWAS_ID_4099,GWAS_ID_4100,GWAS_ID_4101,GWAS_ID_4102,GWAS_ID_4103,GWAS_ID_4104,GWAS_ID_4105,GWAS_ID_4106,GWAS_ID_4107,GWAS_ID_4108,GWAS_ID_4109,GWAS_ID_4110,GWAS_ID_4111,GWAS_ID_4112,GWAS_ID_4113,GWAS_ID_4114,GWAS_ID_4115,GWAS_ID_4116,GWAS_ID_4117,GWAS_ID_4118,GWAS_ID_4119,GWAS_ID_4120,GWAS_ID_4121,GWAS_ID_4122,GWAS_ID_4123,GWAS_ID_4124,GWAS_ID_4125,GWAS_ID_4126,GWAS_ID_4127,GWAS_ID_4128,GWAS_ID_4129,GWAS_ID_4130,GWAS_ID_4131,GWAS_ID_4132,GWAS_ID_4133,GWAS_ID_4134,GWAS_ID_4135,GWAS_ID_4136,GWAS_ID_4137,GWAS_ID_4138,GWAS_ID_4139,GWAS_ID_4140,GWAS_ID_4141,GWAS_ID_4142,GWAS_ID_4143,GWAS_ID_4144,GWAS_ID_4145,GWAS_ID_4146,GWAS_ID_4147,GWAS_ID_4148,GWAS_ID_4149,GWAS_ID_4150,GWAS_ID_4151,GWAS_ID_4152,GWAS_ID_4153,GWAS_ID_4154,GWAS_ID_4155,GWAS_ID_4156,GWAS_ID_4157,GWAS_ID_4158,GWAS_ID_4159,GWAS_ID_4160,GWAS_ID_4161,GWAS_ID_4162,GWAS_ID_4163,GWAS_ID_4164,GWAS_ID_4165,GWAS_ID_4166,GWAS_ID_4167,GWAS_ID_4168,GWAS_ID_4169 RMVar_hsa_circ_124680,RMVar_hsa_circ_125716,RMVar_hsa_circ_137111,RMVar_hsa_circ_137116 37378 RMVar_ID_37378 Human_SNP_ID_36170090 A-to-I Human chr1 + 161143726 161143726 161143726 ACTGAGTCTCGCTCTGTCACCCACGCTGGAGTACAGTGGCACAATCTCAGCTCACTGCAACCTCT ACTGAGTCTCGCTCTGTCACCCACGCTGGAGTGCAGTGGCACAATCTCAGCTCACTGCAACCTCT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1397743401 Functional Loss SNV dbSNP153 33..33 33 - - - 37379 RMVar_ID_37379 Human_SNP_ID_36170245 A-to-I Human chr1 + 161144313 161144313 161144313 GCCTGGCCAACACGGAGAAACCTGTCTCCATTAAAAATACAAAAAGTAGCCGGACGTGGTGTGGG GCCTGGCCAACACGGAGAAACCTGTCTCCATTGAAAATACAAAAAGTAGCCGGACGTGGTGTGGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs926729542 Functional Loss SNV dbSNP153 33..33 33 - - - 37380 RMVar_ID_37380 Human_SNP_ID_36172709 A-to-I Human chr1 + 161153954 161153954 161153954 ATAGTAAAGATGACGGCGCCTTGAGGTAAGCTACAGGCAACACCACTTCCGCGTTTCTCTTGCGC ATAGTAAAGATGACGGCGCCTTGAGGTAAGCTGCAGGCAACACCACTTCCGCGTTTCTCTTGCGC A G UFC1 Ensembl:ENSG00000143222 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs765137972 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_149786 Human_miRNA_ID_2895086 RMVar_hsa_circ_7470,RMVar_hsa_circ_85171,RMVar_hsa_circ_137121,RMVar_hsa_circ_137122 37381 RMVar_ID_37381 Human_SNP_ID_36187223 A-to-I Human chr1 + 161207676 161207676 161207676 TTGAACCTGGGAGGCAGAGGTTGCAGTGAGCCAAGATGGTGCTACTGCACTCCAGCGCCTGGGCA TTGAACCTGGGAGGCAGAGGTTGCAGTGAGCCGAGATGGTGCTACTGCACTCCAGCGCCTGGGCA A G NDUFS2 Ensembl:ENSG00000158864 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965090390 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98482,RMVar_hsa_circ_137137,RMVar_hsa_circ_88006,RMVar_hsa_circ_104088,RMVar_hsa_circ_137138,RMVar_hsa_circ_137139 37382 RMVar_ID_37382 Human_SNP_ID_36187352 A-to-I Human chr1 + 161208059 161208059 161208059 CAGGCTGGAGTGCAATAGTGTGATCTTGGCTCACTGCAAACTCCACCTCCCAGGTTCAAGCGAGT CAGGCTGGAGTGCAATAGTGTGATCTTGGCTCGCTGCAAACTCCACCTCCCAGGTTCAAGCGAGT A G NDUFS2 Ensembl:ENSG00000158864 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1034611953 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98482,RMVar_hsa_circ_137137,RMVar_hsa_circ_88006,RMVar_hsa_circ_104088,RMVar_hsa_circ_137138,RMVar_hsa_circ_137139 37383 RMVar_ID_37383 Human_SNP_ID_36187389 A-to-I Human chr1 + 161208165 161208165 161208165 CACCACCACGCCCAGCTAATTTCTATATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGC CACCACCACGCCCAGCTAATTTCTATATTTTTTGTAGAGATGGGGTTTCACCATGTTGGCCAGGC A T NDUFS2 Ensembl:ENSG00000158864 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1240517753 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98482,RMVar_hsa_circ_137137,RMVar_hsa_circ_88006,RMVar_hsa_circ_104088,RMVar_hsa_circ_137138,RMVar_hsa_circ_137139 37384 RMVar_ID_37384 Human_SNP_ID_36187390 A-to-I Human chr1 + 161208168 161208168 161208168 CACCACGCCCAGCTAATTTCTATATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGG CACCACGCCCAGCTAATTTCTATATTTTTAGTGGAGATGGGGTTTCACCATGTTGGCCAGGCTGG A G NDUFS2 Ensembl:ENSG00000158864 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1377944081 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98482,RMVar_hsa_circ_137137,RMVar_hsa_circ_88006,RMVar_hsa_circ_104088,RMVar_hsa_circ_137138,RMVar_hsa_circ_137139 37385 RMVar_ID_37385 Human_SNP_ID_36188165 A-to-I Human chr1 + 161211014 161211014 161211014 CTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCATGAGCCACCACGCTCAGCTAATTTAT CTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTCCAGGCATGAGCCACCACGCTCAGCTAATTTAT A C NDUFS2 Ensembl:ENSG00000158864 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs746973146 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98482,RMVar_hsa_circ_137137,RMVar_hsa_circ_104088,RMVar_hsa_circ_137138,RMVar_hsa_circ_113883,RMVar_hsa_circ_137142,RMVar_hsa_circ_86395,RMVar_hsa_circ_90216,RMVar_hsa_circ_137144,RMVar_hsa_circ_137145 37386 RMVar_ID_37386 Human_SNP_ID_36188166 A-to-I Human chr1 + 161211014 161211014 161211014 CTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCATGAGCCACCACGCTCAGCTAATTTAT CTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTGCAGGCATGAGCCACCACGCTCAGCTAATTTAT A G NDUFS2 Ensembl:ENSG00000158864 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs746973146 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98482,RMVar_hsa_circ_137137,RMVar_hsa_circ_104088,RMVar_hsa_circ_137138,RMVar_hsa_circ_113883,RMVar_hsa_circ_137142,RMVar_hsa_circ_86395,RMVar_hsa_circ_90216,RMVar_hsa_circ_137144,RMVar_hsa_circ_137145 37387 RMVar_ID_37387 Human_SNP_ID_36189086 A-to-I Human chr1 + 161214301 161214299 161214301 CTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGTTCATGTACACTTGGCTGTCAGGCTTTCTG CTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG__TGTTCATGTACACTTGGCTGTCAGGCTTTCTG GTA G NDUFS2 Ensembl:ENSG00000158864 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886045468 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_21958,Human_RBP_ID_330296,Human_RBP_ID_972068,Human_RBP_ID_1074500,Human_RBP_ID_1414034,Human_RBP_ID_1727528,Human_RBP_ID_4083610,Human_RBP_ID_5136420,Human_RBP_ID_5278588,Human_RBP_ID_5641850,Human_RBP_ID_8288202,Human_RBP_ID_17222853,Human_RBP_ID_17646580,Human_RBP_ID_18554230,Human_RBP_ID_22705519,Human_RBP_ID_22749565,Human_RBP_ID_22872905,Human_RBP_ID_23112385,Human_RBP_ID_23205407,Human_RBP_ID_23338721,Human_RBP_ID_26370424,Human_RBP_ID_26844853,Human_RBP_ID_27170400 Human_miRNA_ID_2728697 Clinvar_Rec_111 RMVar_hsa_circ_113883,RMVar_hsa_circ_137142 37388 RMVar_ID_37388 Human_SNP_ID_36189090 A-to-I Human chr1 + 161214301 161214301 161214301 CTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGTTCATGTACACTTGGCTGTCAGGCTTTCTG CTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTCATGTACACTTGGCTGTCAGGCTTTCTG A G NDUFS2 Ensembl:ENSG00000158864 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs191955041 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21958,Human_RBP_ID_330296,Human_RBP_ID_972068,Human_RBP_ID_1074500,Human_RBP_ID_1414034,Human_RBP_ID_1727528,Human_RBP_ID_4083610,Human_RBP_ID_5136420,Human_RBP_ID_5278588,Human_RBP_ID_5641850,Human_RBP_ID_8288202,Human_RBP_ID_17222853,Human_RBP_ID_17646580,Human_RBP_ID_18554230,Human_RBP_ID_22705519,Human_RBP_ID_22749565,Human_RBP_ID_22872905,Human_RBP_ID_23112385,Human_RBP_ID_23205407,Human_RBP_ID_23338721,Human_RBP_ID_26370424,Human_RBP_ID_26844853,Human_RBP_ID_27170400 Human_miRNA_ID_2728697 Clinvar_Rec_112 RMVar_hsa_circ_113883,RMVar_hsa_circ_137142 37389 RMVar_ID_37389 Human_SNP_ID_36189091 A-to-I Human chr1 + 161214301 161214301 161214301 CTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGTTCATGTACACTTGGCTGTCAGGCTTTCTG CTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTGTTCATGTACACTTGGCTGTCAGGCTTTCTG A T NDUFS2 Ensembl:ENSG00000158864 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs191955041 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21958,Human_RBP_ID_330296,Human_RBP_ID_972068,Human_RBP_ID_1074500,Human_RBP_ID_1414034,Human_RBP_ID_1727528,Human_RBP_ID_4083610,Human_RBP_ID_5136420,Human_RBP_ID_5278588,Human_RBP_ID_5641850,Human_RBP_ID_8288202,Human_RBP_ID_17222853,Human_RBP_ID_17646580,Human_RBP_ID_18554230,Human_RBP_ID_22705519,Human_RBP_ID_22749565,Human_RBP_ID_22872905,Human_RBP_ID_23112385,Human_RBP_ID_23205407,Human_RBP_ID_23338721,Human_RBP_ID_26370424,Human_RBP_ID_26844853,Human_RBP_ID_27170400 Human_miRNA_ID_2728697 Clinvar_Rec_112 RMVar_hsa_circ_113883,RMVar_hsa_circ_137142 37390 RMVar_ID_37390 Human_SNP_ID_36218246 A-to-I Human chr1 + 161326046 161326046 161326046 CAACGTACTGAAACCCCATCTTGACTGAAAATACAAAAATTAGCTGGGCGCGGTGGCATGTGCCT CAACGTACTGAAACCCCATCTTGACTGAAAATGCAAAAATTAGCTGGGCGCGGTGGCATGTGCCT A G SDHC Ensembl:ENSG00000143252 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs773778354 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81462,RMVar_hsa_circ_284782,RMVar_hsa_circ_301479,RMVar_hsa_circ_277045,RMVar_hsa_circ_137155,RMVar_hsa_circ_137157,RMVar_hsa_circ_137158,RMVar_hsa_circ_137156 37391 RMVar_ID_37391 Human_SNP_ID_36221875 A-to-I Human chr1 + 161340168 161340168 161340168 AAAATTAGGCGGACCTGGTGGCAGGCACCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA AAAATTAGGCGGACCTGGTGGCAGGCACCTGTGATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA A G SDHC Ensembl:ENSG00000143252 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1197004186 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81462,RMVar_hsa_circ_301479,RMVar_hsa_circ_277045,RMVar_hsa_circ_137157,RMVar_hsa_circ_137158,RMVar_hsa_circ_137156,RMVar_hsa_circ_122300,RMVar_hsa_circ_137160,RMVar_hsa_circ_60154 37392 RMVar_ID_37392 Human_SNP_ID_36223102 A-to-I Human chr1 + 161345469 161345469 161345469 TTACACAAGTTGTAATTATTTTATTTTATTTTATTTTTGAGACAGAGTCTCGCTTTTCTGCCCAG TTACACAAGTTGTAATTATTTTATTTTATTTTGTTTTTGAGACAGAGTCTCGCTTTTCTGCCCAG A G SDHC Ensembl:ENSG00000143252 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs896795105 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81462,RMVar_hsa_circ_301479,RMVar_hsa_circ_137157,RMVar_hsa_circ_137158 37393 RMVar_ID_37393 Human_SNP_ID_36223164 A-to-I Human chr1 + 161345658 161345658 161345658 TTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTAGCCAGGATGGTCTCGATCTCCTGACCT TTTTGTATTTTTAGTAGAGACAGGGTTTCACCGTGTTAGCCAGGATGGTCTCGATCTCCTGACCT A G SDHC Ensembl:ENSG00000143252 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs935394740 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81462,RMVar_hsa_circ_301479,RMVar_hsa_circ_137157,RMVar_hsa_circ_137158 37394 RMVar_ID_37394 Human_SNP_ID_36228503 A-to-I Human chr1 + 161366975 161366975 161366975 TTTAAATTTACTTGTAGAGACGAGGTCTCACCATATTGCCCAGGGTGGTCTCAAACCCCTGGCCT TTTAAATTTACTTGTAGAGACGAGGTCTCACCGTATTGCCCAGGGTGGTCTCAAACCCCTGGCCT A G - - Other Unknown GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs922672032 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1345143,Human_RBP_ID_10619880 37395 RMVar_ID_37395 Human_SNP_ID_36228504 A-to-I Human chr1 + 161366977 161366977 161366977 TAAATTTACTTGTAGAGACGAGGTCTCACCATATTGCCCAGGGTGGTCTCAAACCCCTGGCCTCA TAAATTTACTTGTAGAGACGAGGTCTCACCATTTTGCCCAGGGTGGTCTCAAACCCCTGGCCTCA A T - - Other Unknown GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs1474079987 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1345143,Human_RBP_ID_10619880 37396 RMVar_ID_37396 Human_SNP_ID_36229262 A-to-I Human chr1 + 161370133 161370133 161370133 AATAAGTAGATAGGCCGGGTGCGGTGGCTCACATCTGTAATCCCAGCACTTTGGGAGGCTGAGGC AATAAGTAGATAGGCCGGGTGCGGTGGCTCACGTCTGTAATCCCAGCACTTTGGGAGGCTGAGGC A G SDHC Ensembl:ENSG00000143252 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1334685477 Functional Loss SNV dbSNP153 33..33 33 - - - 37397 RMVar_ID_37397 Human_SNP_ID_36229300 A-to-I Human chr1 + 161370271 161370271 161370271 AAACATTAGCTGGGCGTGTGGCGGGGGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGA AAACATTAGCTGGGCGTGTGGCGGGGGCCTGTTGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGA A T SDHC Ensembl:ENSG00000143252 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202659399 Functional Loss SNV dbSNP153 33..33 33 - - - 37398 RMVar_ID_37398 Human_SNP_ID_36229302 A-to-I Human chr1 + 161370281 161370281 161370281 TGGGCGTGTGGCGGGGGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATGGCGTGAA TGGGCGTGTGGCGGGGGCCTGTAGTCCCAGCTGCTCAGGAGGCTGAGGCAGGAGAATGGCGTGAA A G SDHC Ensembl:ENSG00000143252 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1007377438 Functional Loss SNV dbSNP153 33..33 33 - - - 37399 RMVar_ID_37399 Human_SNP_ID_36229303 A-to-I Human chr1 + 161370281 161370281 161370281 TGGGCGTGTGGCGGGGGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATGGCGTGAA TGGGCGTGTGGCGGGGGCCTGTAGTCCCAGCTTCTCAGGAGGCTGAGGCAGGAGAATGGCGTGAA A T SDHC Ensembl:ENSG00000143252 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1007377438 Functional Loss SNV dbSNP153 33..33 33 - - - 37400 RMVar_ID_37400 Human_SNP_ID_36229304 A-to-I Human chr1 + 161370285 161370285 161370285 CGTGTGGCGGGGGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATGGCGTGAACCCA CGTGTGGCGGGGGCCTGTAGTCCCAGCTACTCTGGAGGCTGAGGCAGGAGAATGGCGTGAACCCA A T SDHC Ensembl:ENSG00000143252 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1211345008 Functional Loss SNV dbSNP153 33..33 33 - - - 37401 RMVar_ID_37401 Human_SNP_ID_36229495 A-to-I Human chr1 + 161371090 161371090 161371090 CTCAAGTGATTCTTCGACCTCTGGAAGTGTTGAGATTACAGGCACGAGCCACCACACCCACCCAA CTCAAGTGATTCTTCGACCTCTGGAAGTGTTGCGATTACAGGCACGAGCCACCACACCCACCCAA A C SDHC Ensembl:ENSG00000143252 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs534812442 Functional Loss SNV dbSNP153 33..33 33 - - - 37402 RMVar_ID_37402 Human_SNP_ID_36229496 A-to-I Human chr1 + 161371095 161371095 161371095 GTGATTCTTCGACCTCTGGAAGTGTTGAGATTACAGGCACGAGCCACCACACCCACCCAACATGG GTGATTCTTCGACCTCTGGAAGTGTTGAGATTGCAGGCACGAGCCACCACACCCACCCAACATGG A G SDHC Ensembl:ENSG00000143252 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1137632 Functional Loss SNV dbSNP153 33..33 33 - - - 37403 RMVar_ID_37403 Human_SNP_ID_36229549 A-to-I Human chr1 + 161371271 161371271 161371271 CTTACTATTGGGCTGTTGACTTTTTTTTTTGAAACCAGTCCTCCCTCTGTCACCCAGGCTGGAGT CTTACTATTGGGCTGTTGACTTTTTTTTTTGAGACCAGTCCTCCCTCTGTCACCCAGGCTGGAGT A G SDHC Ensembl:ENSG00000143252 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1007756269 Functional Loss SNV dbSNP153 33..33 33 - - - 37404 RMVar_ID_37404 Human_SNP_ID_36229601 A-to-I Human chr1 + 161371505 161371505 161371505 GAACTCCTGGGCTCAAGCCATCTGCCCACCTCAGCTTCCCAAAAAGCTGGGATTACAGGCTTGAG GAACTCCTGGGCTCAAGCCATCTGCCCACCTCCGCTTCCCAAAAAGCTGGGATTACAGGCTTGAG A C SDHC Ensembl:ENSG00000143252 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs578032522 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_833969 37405 RMVar_ID_37405 Human_SNP_ID_36230570 A-to-I Human chr1 + 161374964 161374964 161374964 TTTAGTATTTTTAGTAGAGACAGGGTTTCGCCATGTTGGCCAGGCTGGTCTGGAACTCCTGACGT TTTAGTATTTTTAGTAGAGACAGGGTTTCGCCGTGTTGGCCAGGCTGGTCTGGAACTCCTGACGT A G lnc-SDHC-2 RNACentral:URS00005C37FF lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886458649 Functional Loss SNV dbSNP153 33..33 33 - - - 37406 RMVar_ID_37406 Human_SNP_ID_36230579 A-to-I Human chr1 + 161374998 161374998 161374998 GTTGGCCAGGCTGGTCTGGAACTCCTGACGTCAGGTGATCCACCTGCCTTGGCCTCCCAAAGTCG GTTGGCCAGGCTGGTCTGGAACTCCTGACGTCGGGTGATCCACCTGCCTTGGCCTCCCAAAGTCG A G lnc-SDHC-2 RNACentral:URS00005C37FF lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277786323 Functional Loss SNV dbSNP153 33..33 33 - - - 37407 RMVar_ID_37407 Human_SNP_ID_36241148 A-to-I Human chr1 + 161417188 161417188 161417188 TTGGCTCACTGCAACCTCCACTTCTGAGGTTCAAGTGATTCTCCTGCTTCAGCCTCCTGAATAGC TTGGCTCACTGCAACCTCCACTTCTGAGGTTCCAGTGATTCTCCTGCTTCAGCCTCCTGAATAGC A C AL592295.4 Ensembl:ENSG00000283696 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs970335621 Functional Loss SNV dbSNP153 33..33 33 - - - 37408 RMVar_ID_37408 Human_SNP_ID_36241255 A-to-I Human chr1 + 161417751 161417751 161417751 GACAGATCAATAGGCTGGGCACTGTGACTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGC GACAGATCAATAGGCTGGGCACTGTGACTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGC A G AL592295.4 Ensembl:ENSG00000283696 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1325141654 Functional Loss SNV dbSNP153 33..33 33 - - - 37409 RMVar_ID_37409 Human_SNP_ID_36321882 A-to-I Human chr1 + 161751246 161751246 161751246 CTCCTGCCTCGGCCTCCAGAGTAGCTGGGACTACAGACCCCACCACATCCGGCTAATTTTTTGTA CTCCTGCCTCGGCCTCCAGAGTAGCTGGGACTGCAGACCCCACCACATCCGGCTAATTTTTTGTA A G DUSP12 Ensembl:ENSG00000081721 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs868614012 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88584,RMVar_hsa_circ_137165 37410 RMVar_ID_37410 Human_SNP_ID_36327601 A-to-I Human chr1 + 161775071 161775071 161775071 TGGGCCAGAAATTCTCAGCAAATGAACATGTTAAAAAGAACAAAGGCCCCAATATGAATGAACTC TGGGCCAGAAATTCTCAGCAAATGAACATGTTCAAAAGAACAAAGGCCCCAATATGAATGAACTC A C ATF6 Ensembl:ENSG00000118217 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs762963230 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_137172,RMVar_hsa_circ_79386,RMVar_hsa_circ_88969,RMVar_hsa_circ_137173 37411 RMVar_ID_37411 Human_SNP_ID_36327602 A-to-I Human chr1 + 161775077 161775077 161775077 AGAAATTCTCAGCAAATGAACATGTTAAAAAGAACAAAGGCCCCAATATGAATGAACTCCCCGTG AGAAATTCTCAGCAAATGAACATGTTAAAAAGGACAAAGGCCCCAATATGAATGAACTCCCCGTG A G ATF6 Ensembl:ENSG00000118217 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946036122 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_137172,RMVar_hsa_circ_79386,RMVar_hsa_circ_88969,RMVar_hsa_circ_137173 37412 RMVar_ID_37412 Human_SNP_ID_36327604 A-to-I Human chr1 + 161775080 161775080 161775080 AATTCTCAGCAAATGAACATGTTAAAAAGAACAAAGGCCCCAATATGAATGAACTCCCCGTGGTC AATTCTCAGCAAATGAACATGTTAAAAAGAACGAAGGCCCCAATATGAATGAACTCCCCGTGGTC A G ATF6 Ensembl:ENSG00000118217 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs531310725 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_137172,RMVar_hsa_circ_79386,RMVar_hsa_circ_88969,RMVar_hsa_circ_137173 37413 RMVar_ID_37413 Human_SNP_ID_36327610 A-to-I Human chr1 + 161775092 161775092 161775092 ATGAACATGTTAAAAAGAACAAAGGCCCCAATATGAATGAACTCCCCGTGGTCAAATCTGGGAAA ATGAACATGTTAAAAAGAACAAAGGCCCCAATGTGAATGAACTCCCCGTGGTCAAATCTGGGAAA A G ATF6 Ensembl:ENSG00000118217 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1342826266 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_137172,RMVar_hsa_circ_79386,RMVar_hsa_circ_88969,RMVar_hsa_circ_137173 37414 RMVar_ID_37414 Human_SNP_ID_36348718 A-to-I Human chr1 + 161866887 161866887 161866887 CTCCTGTGTCAGTCTCCAGAGTATCTGGGACTACAGGAGAGTGCCACCACATCCAGCTAATTTTT CTCCTGTGTCAGTCTCCAGAGTATCTGGGACTGCAGGAGAGTGCCACCACATCCAGCTAATTTTT A G ATF6 Ensembl:ENSG00000118217 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027120112 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_308062,RMVar_hsa_circ_21624,RMVar_hsa_circ_341818,RMVar_hsa_circ_375868,RMVar_hsa_circ_105957,RMVar_hsa_circ_137198,RMVar_hsa_circ_137199,RMVar_hsa_circ_306101,RMVar_hsa_circ_137201,RMVar_hsa_circ_137206,RMVar_hsa_circ_295930,RMVar_hsa_circ_29779,RMVar_hsa_circ_137207,RMVar_hsa_circ_294597 37415 RMVar_ID_37415 Human_SNP_ID_36499024 A-to-I Human chr1 + 162506742 162506742 162506742 AAAAAAGTAGCCGGGCCTGGTGGCACGTGCCTATAATCCTAGCTACTCAGGAGGCTGAGGCAGAG AAAAAAGTAGCCGGGCCTGGTGGCACGTGCCTGTAATCCTAGCTACTCAGGAGGCTGAGGCAGAG A G UHMK1 Ensembl:ENSG00000152332 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs570529589 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_137219,RMVar_hsa_circ_309002,RMVar_hsa_circ_307001,RMVar_hsa_circ_137218,RMVar_hsa_circ_296970,RMVar_hsa_circ_287663,RMVar_hsa_circ_137220,RMVar_hsa_circ_137221 37416 RMVar_ID_37416 Human_SNP_ID_36499025 A-to-I Human chr1 + 162506742 162506742 162506742 AAAAAAGTAGCCGGGCCTGGTGGCACGTGCCTATAATCCTAGCTACTCAGGAGGCTGAGGCAGAG AAAAAAGTAGCCGGGCCTGGTGGCACGTGCCTTTAATCCTAGCTACTCAGGAGGCTGAGGCAGAG A T UHMK1 Ensembl:ENSG00000152332 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs570529589 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_137219,RMVar_hsa_circ_309002,RMVar_hsa_circ_307001,RMVar_hsa_circ_137218,RMVar_hsa_circ_296970,RMVar_hsa_circ_287663,RMVar_hsa_circ_137220,RMVar_hsa_circ_137221 37417 RMVar_ID_37417 Human_SNP_ID_36515067 A-to-I Human chr1 + 162573821 162573821 162573821 ACCCCTGTCTACTAAAAATACAAAAATTAGCTAAGTGCGCTGGTGTGCACCTGTAGTCTCAGCTG ACCCCTGTCTACTAAAAATACAAAAATTAGCTCAGTGCGCTGGTGTGCACCTGTAGTCTCAGCTG A C UAP1 Ensembl:ENSG00000117143 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs959630265 Functional Loss SNV dbSNP153 33..33 33 - - - 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_65984,RMVar_hsa_circ_56796,RMVar_hsa_circ_137227,RMVar_hsa_circ_137228 37418 RMVar_ID_37418 Human_SNP_ID_36520100 A-to-I Human chr1 + 162593587 162593587 162593587 CCTGGCAAACATGGCGAAACCTCATCTCTACTAAAAATACAAAAATTAGCTGGTGTGGTCATGCA CCTGGCAAACATGGCGAAACCTCATCTCTACTGAAAATACAAAAATTAGCTGGTGTGGTCATGCA A G UAP1,AL596325.2 Ensembl:ENSG00000117143,Ensembl:ENSG00000272574 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1196513742 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5245645 RMVar_hsa_circ_288800,RMVar_hsa_circ_103345,RMVar_hsa_circ_137228,RMVar_hsa_circ_304815,RMVar_hsa_circ_108581,RMVar_hsa_circ_137232,RMVar_hsa_circ_137233,RMVar_hsa_circ_137231,RMVar_hsa_circ_87439,RMVar_hsa_circ_137234,RMVar_hsa_circ_354971,RMVar_hsa_circ_105773,RMVar_hsa_circ_361767,RMVar_hsa_circ_365802,RMVar_hsa_circ_137238,RMVar_hsa_circ_54273 37419 RMVar_ID_37419 Human_SNP_ID_36689889 A-to-I Human chr1 - 163310953 163310953 163310953 GATATTGAGTTGTCATGAGATCTGACGGTTTTATAAGGGGCTCTTCCCCCTTTGCTCGGCATTTC GATATTGAGTTGTCATGAGATCTGACGGTTTTTTAAGGGGCTCTTCCCCCTTTGCTCGGCATTTC T A RGS5,AL592435.1 Ensembl:ENSG00000143248,Ensembl:ENSG00000232995 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs983893530 Functional Loss SNV dbSNP153 33..33 33 - - - 37420 RMVar_ID_37420 Human_SNP_ID_37003079 A-to-I Human chr1 + 164589579 164589579 164589579 CAGAGTGCTAAATGATCCCCTGGTGCCCTGGAAAGAGACCGTTTACCTCCAAAAGGTGAGTTGTT CAGAGTGCTAAATGATCCCCTGGTGCCCTGGACAGAGACCGTTTACCTCCAAAAGGTGAGTTGTT A C PBX1 Ensembl:ENSG00000185630 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1379150445 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74927,RMVar_hsa_circ_329982 37421 RMVar_ID_37421 Human_SNP_ID_37004302 A-to-I Human chr1 + 164594463 164594463 164594463 ATTACAGGCACCTGCCAAATTTTTGTATTTTTAGTGGAGACGGGGTTTCGCCGTGTTGGCCAGGC ATTACAGGCACCTGCCAAATTTTTGTATTTTTCGTGGAGACGGGGTTTCGCCGTGTTGGCCAGGC A C PBX1 Ensembl:ENSG00000185630 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs766810131 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2099701,Human_RBP_ID_10628853 RMVar_hsa_circ_74927,RMVar_hsa_circ_329982 37422 RMVar_ID_37422 Human_SNP_ID_37004303 A-to-I Human chr1 + 164594463 164594463 164594463 ATTACAGGCACCTGCCAAATTTTTGTATTTTTAGTGGAGACGGGGTTTCGCCGTGTTGGCCAGGC ATTACAGGCACCTGCCAAATTTTTGTATTTTTGGTGGAGACGGGGTTTCGCCGTGTTGGCCAGGC A G PBX1 Ensembl:ENSG00000185630 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs766810131 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2099701,Human_RBP_ID_10628853 RMVar_hsa_circ_74927,RMVar_hsa_circ_329982 37423 RMVar_ID_37423 Human_SNP_ID_37005795 A-to-I Human chr1 + 164601118 164601118 164601118 AAAATTAGCCGGGCGTGGCGGTGGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGAAAGAATT AAAATTAGCCGGGCGTGGCGGTGGGCGCCTGTGGTCCCAGCTACTCGGGAGGCTGAGAAAGAATT A G PBX1 Ensembl:ENSG00000185630 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1192472087 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74927,RMVar_hsa_circ_329982 37424 RMVar_ID_37424 Human_SNP_ID_37020236 A-to-I Human chr1 + 164661566 164661566 164661566 CTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCCTCCACCACCATGCCTGGCAAATTTTT CTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTTCAGGCCTCCACCACCATGCCTGGCAAATTTTT A T PBX1 Ensembl:ENSG00000185630 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1165801073 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41542,RMVar_hsa_circ_74927,RMVar_hsa_circ_329982 37425 RMVar_ID_37425 Human_SNP_ID_417978731 A-to-I Human chr9 + 135910003 135910003 135910003 GCTGGTCTTGAACTCCTGACCTCCAGTAATCCACCCCCCTGGGCCTCCCAAAATGCTGGGATTAT GCTGGTCTTGAACTCCTGACCTCCAGTAATCCCCCCCCCTGGGCCTCCCAAAATGCTGGGATTAT A C AL355574.1 Ensembl:ENSG00000238058 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1373407973 Functional Loss SNV dbSNP153 33..33 33 - - - 37426 RMVar_ID_37426 Human_SNP_ID_417986278 A-to-I Human chr9 - 135935004 135935002 135935004 GGTGGCACACGTACCTGTAGTCCCTGCTACTCAGGGGACTGAGGTGGGAGGATCATTGAGTCTGG GGTGGCACACGTACCTGTAGTCCCTGCTACTC__GGGACTGAGGTGGGAGGATCATTGAGTCTGG CCT C UBAC1 Ensembl:ENSG00000130560 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs371978443 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_98326,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_260819,RMVar_hsa_circ_260818,RMVar_hsa_circ_260815,RMVar_hsa_circ_260816,RMVar_hsa_circ_260814,RMVar_hsa_circ_260822,RMVar_hsa_circ_260812 37427 RMVar_ID_37427 Human_SNP_ID_417986280 A-to-I Human chr9 - 135935004 135935004 135935004 GGTGGCACACGTACCTGTAGTCCCTGCTACTCAGGGGACTGAGGTGGGAGGATCATTGAGTCTGG GGTGGCACACGTACCTGTAGTCCCTGCTACTCGGGGGACTGAGGTGGGAGGATCATTGAGTCTGG T C UBAC1 Ensembl:ENSG00000130560 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1034156649 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98326,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_260819,RMVar_hsa_circ_260818,RMVar_hsa_circ_260815,RMVar_hsa_circ_260816,RMVar_hsa_circ_260814,RMVar_hsa_circ_260822,RMVar_hsa_circ_260812 37428 RMVar_ID_37428 Human_SNP_ID_417986281 A-to-I Human chr9 - 135935004 135935004 135935004 GGTGGCACACGTACCTGTAGTCCCTGCTACTCAGGGGACTGAGGTGGGAGGATCATTGAGTCTGG GGTGGCACACGTACCTGTAGTCCCTGCTACTCCGGGGACTGAGGTGGGAGGATCATTGAGTCTGG T G UBAC1 Ensembl:ENSG00000130560 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1034156649 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98326,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_260819,RMVar_hsa_circ_260818,RMVar_hsa_circ_260815,RMVar_hsa_circ_260816,RMVar_hsa_circ_260814,RMVar_hsa_circ_260822,RMVar_hsa_circ_260812 37429 RMVar_ID_37429 Human_SNP_ID_418007203 A-to-I Human chr9 - 136007293 136007293 136007293 GGAGCATTTAGGGTTTGGTACAAGATGGTTCTAAAATGGCAAAGGTTTTTCGTGTTTGTTTGTTT GGAGCATTTAGGGTTTGGTACAAGATGGTTCTCAAATGGCAAAGGTTTTTCGTGTTTGTTTGTTT T G NACC2 Ensembl:ENSG00000148411 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1246776611 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18397058,Human_RBP_ID_24292364 RMVar_hsa_circ_127352,RMVar_hsa_circ_260832 37430 RMVar_ID_37430 Human_SNP_ID_418039939 A-to-I Human chr9 - 136113160 136113160 136113160 GTTTGAGCCCAGGCCGGGGAGGGGTTGAGGCTACAGTGAACCATGATTTTGTCACTGCTCCACCC GTTTGAGCCCAGGCCGGGGAGGGGTTGAGGCTGCAGTGAACCATGATTTTGTCACTGCTCCACCC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1255794454 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_714863,Human_RBP_ID_17716184,Human_RBP_ID_18132192 37431 RMVar_ID_37431 Human_SNP_ID_418069980 A-to-I Human chr9 - 136209700 136209700 136209700 AGGTGGCCGGGGCTCTGTAGGTAGTGGGCCTCAGGTGCACCCTCAGGAAAGGGCAGAGGGGCAGC AGGTGGCCGGGGCTCTGTAGGTAGTGGGCCTCTGGTGCACCCTCAGGAAAGGGCAGAGGGGCAGC T A QSOX2 Ensembl:ENSG00000165661 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs562288313 Functional Loss SNV dbSNP153 33..33 33 - - - 37432 RMVar_ID_37432 Human_SNP_ID_418069981 A-to-I Human chr9 - 136209700 136209700 136209700 AGGTGGCCGGGGCTCTGTAGGTAGTGGGCCTCAGGTGCACCCTCAGGAAAGGGCAGAGGGGCAGC AGGTGGCCGGGGCTCTGTAGGTAGTGGGCCTCGGGTGCACCCTCAGGAAAGGGCAGAGGGGCAGC T C QSOX2 Ensembl:ENSG00000165661 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs562288313 Functional Loss SNV dbSNP153 33..33 33 - - - 37433 RMVar_ID_37433 Human_SNP_ID_418073058 A-to-I Human chr9 - 136220046 136220046 136220046 GCCTGGGCAACAGAGAAAGATCCTGTCTCAAAAATAGATAAATGAGTGAAAATACAAAAGATAAA GCCTGGGCAACAGAGAAAGATCCTGTCTCAAAGATAGATAAATGAGTGAAAATACAAAAGATAAA T C QSOX2 Ensembl:ENSG00000165661 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1040835034 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4634,RMVar_hsa_circ_111119,RMVar_hsa_circ_260838,RMVar_hsa_circ_329603,RMVar_hsa_circ_260840,RMVar_hsa_circ_260841 37434 RMVar_ID_37434 Human_SNP_ID_418116024 A-to-I Human chr9 - 136363567 136363567 136363567 GGCGGGCCTGGGCCTGGGGCTGGCGGCGCTCAAGCTCCGAGCAGGGGCCGGGGCCCGCGGCGGCT GGCGGGCCTGGGCCTGGGGCTGGCGGCGCTCACGCTCCGAGCAGGGGCCGGGGCCCGCGGCGGCT T G DNLZ,CARD9 Ensembl:ENSG00000213221,Ensembl:ENSG00000187796 Protein coding,Protein coding CDS,exon GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs778158039 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1099187,Human_Splice_Rec_1099189 37435 RMVar_ID_37435 Human_SNP_ID_418132577 A-to-I Human chr9 - 136406519 136406519 136406519 TGAGCCGAGGTCACGCCACTGTACTCCAGCCTAGGCGACGGGCGAAACTCTGTTTCAAAAAAAAG TGAGCCGAGGTCACGCCACTGTACTCCAGCCTGGGCGACGGGCGAAACTCTGTTTCAAAAAAAAG T C ENTR1 Ensembl:ENSG00000165689 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs549019888 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17579418,Human_RBP_ID_23200823,Human_RBP_ID_26211377 RMVar_hsa_circ_51422,RMVar_hsa_circ_70092,RMVar_hsa_circ_260862,RMVar_hsa_circ_114249,RMVar_hsa_circ_360018,RMVar_hsa_circ_61004 37436 RMVar_ID_37436 Human_SNP_ID_418133956 A-to-I Human chr9 - 136409365 136409365 136409365 CATCCTGGCTAACAGGGTGAAAACCCGTCTCTACAAAAAATACAAAAAAATTAGCCGGGCGTGGT CATCCTGGCTAACAGGGTGAAAACCCGTCTCTGCAAAAAATACAAAAAAATTAGCCGGGCGTGGT T C ENTR1 Ensembl:ENSG00000165689 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1159565424 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26242284 RMVar_hsa_circ_260862,RMVar_hsa_circ_114249,RMVar_hsa_circ_360018 37437 RMVar_ID_37437 Human_SNP_ID_418133978 A-to-I Human chr9 - 136409427 136409427 136409427 CCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGCGGATCATGAGGTCAGGAGATTGAGACCAT CCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGGATCATGAGGTCAGGAGATTGAGACCAT T C ENTR1 Ensembl:ENSG00000165689 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1436982518 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_260862,RMVar_hsa_circ_114249,RMVar_hsa_circ_360018 37438 RMVar_ID_37438 Human_SNP_ID_418136210 A-to-I Human chr9 + 136415672 136415672 136415672 GTTTCTTTTTGGAGATAGAGTCTGTCTCTGTCACCCAGGCTGGAATGCAGTGGCGCGATCTCGGC GTTTCTTTTTGGAGATAGAGTCTGTCTCTGTCGCCCAGGCTGGAATGCAGTGGCGCGATCTCGGC A G PMPCA Ensembl:ENSG00000165688 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs532401866 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_183577 RMVar_hsa_circ_26742,RMVar_hsa_circ_117154,RMVar_hsa_circ_260863 37439 RMVar_ID_37439 Human_SNP_ID_418145624 A-to-I Human chr9 - 136441430 136441430 136441430 TTCCTGGTCATTTAAGAATGTTCATTCATTGAAGCCGGAGCTGTCTCTGCCACAGGAGAGCCACA TTCCTGGTCATTTAAGAATGTTCATTCATTGAGGCCGGAGCTGTCTCTGCCACAGGAGAGCCACA T C SEC16A Ensembl:ENSG00000148396 Protein coding exon GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1802979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2062206,Human_RBP_ID_5124478,Human_RBP_ID_7907698,Human_RBP_ID_8927239,Human_RBP_ID_9315341,Human_RBP_ID_16616055,Human_RBP_ID_17321681,Human_RBP_ID_17435906,Human_RBP_ID_17549005,Human_RBP_ID_18397109,Human_RBP_ID_26566311,Human_RBP_ID_27547777 37440 RMVar_ID_37440 Human_SNP_ID_418147660 A-to-I Human chr9 - 136448135 136448135 136448135 ATTTAGGGTGAATCCTGGTTCTTTCGTTGGCTACCTGGAAAGAAAAAGACAGAAGCTTATTTGCC ATTTAGGGTGAATCCTGGTTCTTTCGTTGGCTGCCTGGAAAGAAAAAGACAGAAGCTTATTTGCC T C SEC16A Ensembl:ENSG00000148396 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs759948957 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_91519,Human_RBP_ID_2062209,Human_RBP_ID_8700023,Human_RBP_ID_8927259,Human_RBP_ID_18905985,Human_RBP_ID_26239774,Human_RBP_ID_27544241 Human_Splice_Rec_1099656,Human_Splice_Rec_1099657,Human_Splice_Rec_1099716,Human_Splice_Rec_1099717,Human_Splice_Rec_1099752,Human_Splice_Rec_1099753,Human_Splice_Rec_1099804,Human_Splice_Rec_1099805,Human_Splice_Rec_1099860,Human_Splice_Rec_1099861,Human_Splice_Rec_1099874,Human_Splice_Rec_1099875,Human_Splice_Rec_1099932,Human_Splice_Rec_1099933 Human_miRNA_ID_2668064 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,RMVar_hsa_circ_61233 37441 RMVar_ID_37441 Human_SNP_ID_418148076 A-to-I Human chr9 - 136449353 136449353 136449353 CCCAGCTACTCAGGAGGTTGAGGCATAGAACTACTTGAACCCGGGAGGCAGAGGTTGCAGTGCGC CCCAGCTACTCAGGAGGTTGAGGCATAGAACTGCTTGAACCCGGGAGGCAGAGGTTGCAGTGCGC T C SEC16A Ensembl:ENSG00000148396 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1030926695 Functional Loss SNV dbSNP153 33..33 33 - - - 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 37442 RMVar_ID_37442 Human_SNP_ID_418153264 A-to-I Human chr9 - 136466051 136466051 136466051 TCCTCCAGGCTCCTTTCACGGCGATTTTGCCTACGGCACCTACCGCAGCAATTTCAGCAGTGGCC TCCTCCAGGCTCCTTTCACGGCGATTTTGCCTGCGGCACCTACCGCAGCAATTTCAGCAGTGGCC T C SEC16A Ensembl:ENSG00000148396 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1564505831 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1058604,Human_RBP_ID_9408865,Human_RBP_ID_22119505 Human_Splice_Rec_1099624,Human_Splice_Rec_1099625,Human_Splice_Rec_1099684,Human_Splice_Rec_1099685,Human_Splice_Rec_1099772,Human_Splice_Rec_1099773,Human_Splice_Rec_1099828,Human_Splice_Rec_1099829,Human_Splice_Rec_1099900,Human_Splice_Rec_1099901,Human_Splice_Rec_1099947 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 37443 RMVar_ID_37443 Human_SNP_ID_418184721 A-to-I Human chr9 + 136557657 136557657 136557657 GAATTCCTGGGCTCAAACAATCCTCCTGCCTCAGCCTCCCAAGTTACTAGGACTACAGGTGCACC GAATTCCTGGGCTCAAACAATCCTCCTGCCTCCGCCTCCCAAGTTACTAGGACTACAGGTGCACC A C NALT1,NALT1:2,NALT1:3,NALT1:4,NALT1:5,NALT1:6,NALT1:7,NALT1:8,NALT1:9 RNACentral:URS0000D5D604,RNACentral:URS0000D5CFE4,RNACentral:URS0000D57F18,RNACentral:URS0000D572F5,RNACentral:URS0000D5BCC1,RNACentral:URS0000D59AA5,RNACentral:URS0000D57366,RNACentral:URS0000D57DE7,RNACentral:URS0000D5C184 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,exon,exon,exon,exon,exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1455312554 Functional Loss SNV dbSNP153 33..33 33 - - - 37444 RMVar_ID_37444 Human_SNP_ID_418210990 A-to-I Human chr9 - 136639771 136639771 136639771 GTGGTGGCAGGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAGACAGGAGAATTGCCTAAACCCG GTGGTGGCAGGCGCCTGTAATCCCAGCTACTCGGGAGGCTGAGACAGGAGAATTGCCTAAACCCG T C RF00017-4674 RNACentral:URS000094E2D9 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1420797994 Functional Loss SNV dbSNP153 33..33 33 - - - 37445 RMVar_ID_37445 Human_SNP_ID_418262208 A-to-I Human chr9 - 136801584 136801584 136801584 CTCGTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCATGCACCACCATGCCAGGCTACTTTTT CTCGTGCCTCAGCCTCCCGAGTAGCTGGGATTCCAGGCATGCACCACCATGCCAGGCTACTTTTT T G 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,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1368792506 Functional Loss SNV dbSNP153 33..33 33 - - - 37446 RMVar_ID_37446 Human_SNP_ID_418262318 A-to-I Human chr9 - 136802061 136802061 136802061 AGTATAGGCCAGGTGCGGTGGCTCACGCCTGTAATCCCAACACTGGGAGGCCGGAGGCAGGCAGA AGTATAGGCCAGGTGCGGTGGCTCACGCCTGTGATCCCAACACTGGGAGGCCGGAGGCAGGCAGA 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,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1163098552 Functional Loss SNV dbSNP153 33..33 33 - - - 37447 RMVar_ID_37447 Human_SNP_ID_418270668 A-to-I Human chr9 + 136825790 136825790 136825790 TTAGGATTCTCCCTGTTTCAGCCACGGATGACATCGTGAAGGTTGAAGTCTGGGATGTAGTAGAC TTAGGATTCTCCCTGTTTCAGCCACGGATGACGTCGTGAAGGTTGAAGTCTGGGATGTAGTAGAC A G AL355987.2,RABL6 Ensembl:ENSG00000272679,Ensembl:ENSG00000196642 lincRNA,Protein coding exon,CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs867464647 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_90064,Human_RBP_ID_1118424,Human_RBP_ID_1703495,Human_RBP_ID_2062257,Human_RBP_ID_3911080,Human_RBP_ID_5020734,Human_RBP_ID_5633942,Human_RBP_ID_7952061,Human_RBP_ID_9315392,Human_RBP_ID_9407805,Human_RBP_ID_16617384,Human_RBP_ID_18414565,Human_RBP_ID_18906072,Human_RBP_ID_19026135,Human_RBP_ID_22556437,Human_RBP_ID_22690631,Human_RBP_ID_23091104 Human_Splice_Rec_1100646,Human_Splice_Rec_1100647,Human_Splice_Rec_1100662,Human_Splice_Rec_1100663,Human_Splice_Rec_1100676,Human_Splice_Rec_1100677,Human_Splice_Rec_1100704,Human_Splice_Rec_1100705,Human_Splice_Rec_1100730,Human_Splice_Rec_1100731,Human_Splice_Rec_1100758,Human_Splice_Rec_1100759,Human_Splice_Rec_1100774,Human_Splice_Rec_1100775,Human_Splice_Rec_1100802,Human_Splice_Rec_1100803,Human_Splice_Rec_1100822,Human_Splice_Rec_1100823 Human_miRNA_ID_2745219,Human_miRNA_ID_3193714 RMVar_hsa_circ_24332,RMVar_hsa_circ_291256,RMVar_hsa_circ_260907,RMVar_hsa_circ_88767,RMVar_hsa_circ_318358,RMVar_hsa_circ_350465,RMVar_hsa_circ_78953,RMVar_hsa_circ_84176,RMVar_hsa_circ_260909,RMVar_hsa_circ_260911,RMVar_hsa_circ_260912,RMVar_hsa_circ_260910 37448 RMVar_ID_37448 Human_SNP_ID_418273709 A-to-I Human chr9 - 136834705 136834705 136834705 GGGGGGGCCAAGGCGGGCAGATCACGAGGTCAAGAGATCGAGACCGTCCTGGCCAATATGGCAAA GGGGGGGCCAAGGCGGGCAGATCACGAGGTCAGGAGATCGAGACCGTCCTGGCCAATATGGCAAA T C CCDC183-AS1 RNACentral:URS00009BEEB0 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs565295058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16617486 37449 RMVar_ID_37449 Human_SNP_ID_418287595 A-to-I Human chr9 + 136867066 136867066 136867066 AACGCAAGCCGGGCACGGTGGTTCACGCCTGTAGTCCCAGAACTTTGGGAGGCCGAGGCGGGCGT AACGCAAGCCGGGCACGGTGGTTCACGCCTGTGGTCCCAGAACTTTGGGAGGCCGAGGCGGGCGT A G lnc-MAMDC4-4,lnc-MAMDC4-4:2 RNACentral:URS0000D5A509,RNACentral:URS0000D5C39F lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1341580068 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7907882 37450 RMVar_ID_37450 Human_SNP_ID_418288434 A-to-I Human chr9 + 136869915 136869915 136869915 TTTTTTGAGATGGAGTTTCGCTCTTGTCATCCAGACTGGAGTGCAGTGACATGATCTAGGCTCAC TTTTTTGAGATGGAGTTTCGCTCTTGTCATCCGGACTGGAGTGCAGTGACATGATCTAGGCTCAC A G lnc-MAMDC4-4,lnc-MAMDC4-4:2 RNACentral:URS0000D5A509,RNACentral:URS0000D5C39F lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1020185709 Functional Loss SNV dbSNP153 33..33 33 - - - 37451 RMVar_ID_37451 Human_SNP_ID_418293726 A-to-I Human chr9 + 136888139 136888139 136888139 GTGATCCACCCGCCTCGGCCTCCCAAAGTGCTAGGATTACAGGCATGAGCCACCGCGCCCGGCCA GTGATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCGCCCGGCCA A G TRAF2 Ensembl:ENSG00000127191 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs201278489 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16617709 37452 RMVar_ID_37452 Human_SNP_ID_418293776 A-to-I Human chr9 + 136888310 136888310 136888310 GTGGGTTAGAATCAGGTGCCATTGACGCCTGTAGTCCCAGCTACTCCGGAGGCTGAGGCAGGAGA GTGGGTTAGAATCAGGTGCCATTGACGCCTGTGGTCCCAGCTACTCCGGAGGCTGAGGCAGGAGA A G TRAF2 Ensembl:ENSG00000127191 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1029962505 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_184602 37453 RMVar_ID_37453 Human_SNP_ID_418294717 A-to-I Human chr9 + 136891030 136891030 136891030 AGTGGCTGGGACCACAGATGCGAGATCCTCCCACCTCGGCCTCCTGAGTAGCTGGGACCACAGAT AGTGGCTGGGACCACAGATGCGAGATCCTCCCGCCTCGGCCTCCTGAGTAGCTGGGACCACAGAT A G TRAF2 Ensembl:ENSG00000127191 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1447288505 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_305064 37454 RMVar_ID_37454 Human_SNP_ID_418294751 A-to-I Human chr9 + 136891178 136891178 136891178 TTGCTCAGGCTGGAGTGCAGTGGCATGATCTCAGCTCACTGCAACCTCCGCCTCTCAGGTTTGAG TTGCTCAGGCTGGAGTGCAGTGGCATGATCTCGGCTCACTGCAACCTCCGCCTCTCAGGTTTGAG A G TRAF2 Ensembl:ENSG00000127191 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs955935626 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_305064 37455 RMVar_ID_37455 Human_SNP_ID_418294770 A-to-I Human chr9 + 136891284 136891284 136891284 GCTTGCACCACCATGCCTGGCTAATTTTTTGTATTTTTAGTGGAGACGGGGTCTCACCATGTTGG GCTTGCACCACCATGCCTGGCTAATTTTTTGTGTTTTTAGTGGAGACGGGGTCTCACCATGTTGG A G TRAF2 Ensembl:ENSG00000127191 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs913323123 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16617846 RMVar_hsa_circ_305064 37456 RMVar_ID_37456 Human_SNP_ID_418294771 A-to-I Human chr9 + 136891290 136891290 136891290 ACCACCATGCCTGGCTAATTTTTTGTATTTTTAGTGGAGACGGGGTCTCACCATGTTGGCCAGCC ACCACCATGCCTGGCTAATTTTTTGTATTTTTGGTGGAGACGGGGTCTCACCATGTTGGCCAGCC A G TRAF2 Ensembl:ENSG00000127191 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs946169089 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16617846 RMVar_hsa_circ_305064 37457 RMVar_ID_37457 Human_SNP_ID_418294780 A-to-I Human chr9 + 136891310 136891310 136891310 TTTTGTATTTTTAGTGGAGACGGGGTCTCACCATGTTGGCCAGCCTGGTCTTGAACTCCTGACCT TTTTGTATTTTTAGTGGAGACGGGGTCTCACCGTGTTGGCCAGCCTGGTCTTGAACTCCTGACCT A G TRAF2 Ensembl:ENSG00000127191 Protein coding intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1201236610 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16617848 RMVar_hsa_circ_305064 37458 RMVar_ID_37458 Human_SNP_ID_418294819 A-to-I Human chr9 + 136891433 136891433 136891433 CCCAGCCATTTTTTTGTGTTTTTGGTAGAGACAGGGTTTCATCATGTTCCCCAGGCTGGTCTTGA CCCAGCCATTTTTTTGTGTTTTTGGTAGAGACGGGGTTTCATCATGTTCCCCAGGCTGGTCTTGA A G TRAF2 Ensembl:ENSG00000127191 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1436253471 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_305064 37459 RMVar_ID_37459 Human_SNP_ID_418294828 A-to-I Human chr9 + 136891478 136891478 136891478 GTTCCCCAGGCTGGTCTTGAACTCCTGAGCTCAAGCAATCTGCCTACCTCGGCCTCCCAAAGTGC GTTCCCCAGGCTGGTCTTGAACTCCTGAGCTCGAGCAATCTGCCTACCTCGGCCTCCCAAAGTGC A G TRAF2 Ensembl:ENSG00000127191 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1375612773 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_305064 37460 RMVar_ID_37460 Human_SNP_ID_418294837 A-to-I Human chr9 + 136891505 136891505 136891505 AGCTCAAGCAATCTGCCTACCTCGGCCTCCCAAAGTGCTGGGATTATAGGTGTGAGCCACCATGC AGCTCAAGCAATCTGCCTACCTCGGCCTCCCAGAGTGCTGGGATTATAGGTGTGAGCCACCATGC A G TRAF2 Ensembl:ENSG00000127191 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1020280190 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_305064 37461 RMVar_ID_37461 Human_SNP_ID_418294956 A-to-I Human chr9 + 136891887 136891887 136891887 GGAATTACAGGCGTGAGCCACTGCACTCGGCTAATTTTGTGTTTTTAGTAGAAATGGGTTTCTCC GGAATTACAGGCGTGAGCCACTGCACTCGGCTCATTTTGTGTTTTTAGTAGAAATGGGTTTCTCC A C TRAF2 Ensembl:ENSG00000127191 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs988133363 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_305064 37462 RMVar_ID_37462 Human_SNP_ID_418294957 A-to-I Human chr9 + 136891887 136891887 136891887 GGAATTACAGGCGTGAGCCACTGCACTCGGCTAATTTTGTGTTTTTAGTAGAAATGGGTTTCTCC GGAATTACAGGCGTGAGCCACTGCACTCGGCTGATTTTGTGTTTTTAGTAGAAATGGGTTTCTCC A G TRAF2 Ensembl:ENSG00000127191 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs988133363 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_305064 37463 RMVar_ID_37463 Human_SNP_ID_418295156 A-to-I Human chr9 + 136892622 136892622 136892622 AGTGGCTCAGCCAGGCACAGTGGCTCATGCCTATAATCTCAGCACTTTGGGAGATTGAGGTGGGC AGTGGCTCAGCCAGGCACAGTGGCTCATGCCTGTAATCTCAGCACTTTGGGAGATTGAGGTGGGC A G TRAF2 Ensembl:ENSG00000127191 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1040342858 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1247760,Human_RBP_ID_16617889 RMVar_hsa_circ_305064 37464 RMVar_ID_37464 Human_SNP_ID_418295157 A-to-I Human chr9 + 136892624 136892624 136892624 TGGCTCAGCCAGGCACAGTGGCTCATGCCTATAATCTCAGCACTTTGGGAGATTGAGGTGGGCAG TGGCTCAGCCAGGCACAGTGGCTCATGCCTATCATCTCAGCACTTTGGGAGATTGAGGTGGGCAG A C TRAF2 Ensembl:ENSG00000127191 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs545584294 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1247760,Human_RBP_ID_16617889 RMVar_hsa_circ_305064 37465 RMVar_ID_37465 Human_SNP_ID_418295193 A-to-I Human chr9 + 136892759 136892759 136892759 AAAATTAGCCAGGCGTGGTGACAGGCGTCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTAGCCAGGCGTGGTGACAGGCGTCTGTTATCCCAGCTACTCGGGAGGCTGAGGCAGGAGA A T TRAF2 Ensembl:ENSG00000127191 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1034392625 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_305064 37466 RMVar_ID_37466 Human_SNP_ID_418295562 A-to-I Human chr9 + 136893950 136893950 136893950 TTTTGTATTTTTACTAGAGATGGGGTTTCACCATGTTGGTCGGGCTGGTCTCAAACTCCTGACCT TTTTGTATTTTTACTAGAGATGGGGTTTCACCGTGTTGGTCGGGCTGGTCTCAAACTCCTGACCT A G TRAF2 Ensembl:ENSG00000127191 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs953010787 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_305064 37467 RMVar_ID_37467 Human_SNP_ID_418295640 A-to-I Human chr9 + 136894176 136894169 136894176 TCAAGCAATTCTCCTGCTTCAGCCTCCACAGTAGCTGGGATTACAGGCACACACCACAATGTCCG TCAAGCAATTCTCCTGCTTCAGCCTC_______GCTGGGATTACAGGCACACACCACAATGTCCG CCACAGTA C TRAF2 Ensembl:ENSG00000127191 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1207502373 Functional Loss DEL dbSNP153 27..33 33 - - - RMVar_hsa_circ_305064 37468 RMVar_ID_37468 Human_SNP_ID_418296018 A-to-I Human chr9 + 136895581 136895581 136895581 ATTTGTCATTTAAATGTTGGAATGGGCCAGGCACGGTGGCTCCTACCTGGAATCCCAGCACATTG ATTTGTCATTTAAATGTTGGAATGGGCCAGGCGCGGTGGCTCCTACCTGGAATCCCAGCACATTG A G TRAF2 Ensembl:ENSG00000127191 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1244243283 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16618014 RMVar_hsa_circ_305064 37469 RMVar_ID_37469 Human_SNP_ID_418296027 A-to-I Human chr9 + 136895599 136895599 136895599 GGAATGGGCCAGGCACGGTGGCTCCTACCTGGAATCCCAGCACATTGGGAGGGCAAGGTTGGATC GGAATGGGCCAGGCACGGTGGCTCCTACCTGGTATCCCAGCACATTGGGAGGGCAAGGTTGGATC A T TRAF2 Ensembl:ENSG00000127191 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388273060 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16618014 RMVar_hsa_circ_305064 37470 RMVar_ID_37470 Human_SNP_ID_418302215 A-to-I Human chr9 + 136912794 136912794 136912794 AGGAGGTGGAGGTTGCAGTGAGCTGAGATCGCACCACTGCACTCCAGCCTGGGTGACAGAGTGAG AGGAGGTGGAGGTTGCAGTGAGCTGAGATCGCTCCACTGCACTCCAGCCTGGGTGACAGAGTGAG A T TRAF2 Ensembl:ENSG00000127191 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs765197213 Functional Loss SNV dbSNP153 33..33 33 - - - 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 37471 RMVar_ID_37471 Human_SNP_ID_418302255 A-to-I Human chr9 + 136912946 136912946 136912946 CCTGAGGTCAGGAGATCAAAACCAGCCTGTCCAACATGGCAAAACCCCTTCTCTACTAAAAATAC CCTGAGGTCAGGAGATCAAAACCAGCCTGTCCGACATGGCAAAACCCCTTCTCTACTAAAAATAC A G TRAF2 Ensembl:ENSG00000127191 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs535397851 Functional Loss SNV dbSNP153 33..33 33 - - - 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 37472 RMVar_ID_37472 Human_SNP_ID_418302272 A-to-I Human chr9 + 136913016 136913016 136913016 TTAGCCAGGTGTGGTGGCACAGGCACTCCTGTAATCCCAGCTACTTGGGAAGCTGAGACAGGAGA TTAGCCAGGTGTGGTGGCACAGGCACTCCTGTGATCCCAGCTACTTGGGAAGCTGAGACAGGAGA A G TRAF2 Ensembl:ENSG00000127191 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1265412004 Functional Loss SNV dbSNP153 33..33 33 - - - 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 37473 RMVar_ID_37473 Human_SNP_ID_418304394 A-to-I Human chr9 + 136919317 136919317 136919317 TTGTGGGTGGCTTTTTTTTTTTTTTTTTTTTGAGACAGAGTTTCGCTCTTGTTGCCCAGACTAGA TTGTGGGTGGCTTTTTTTTTTTTTTTTTTTTGTGACAGAGTTTCGCTCTTGTTGCCCAGACTAGA A T TRAF2 Ensembl:ENSG00000127191 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1349280645 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16618437 RMVar_hsa_circ_5399,RMVar_hsa_circ_260937,RMVar_hsa_circ_108701,RMVar_hsa_circ_107198,RMVar_hsa_circ_260942 37474 RMVar_ID_37474 Human_SNP_ID_418306255 A-to-I Human chr9 + 136924415 136924415 136924415 GAACCCATGTCTACAAAAAAAATAGAAAAATTAGCCGGGCATGGTGGTGTGCACCTGTATTCCCA GAACCCATGTCTACAAAAAAAATAGAAAAATTCGCCGGGCATGGTGGTGTGCACCTGTATTCCCA A C TRAF2 Ensembl:ENSG00000127191 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1564423494 Functional Loss SNV dbSNP153 33..33 33 - - - 37475 RMVar_ID_37475 Human_SNP_ID_418310302 A-to-I Human chr9 + 136936124 136936124 136936124 GGTCAGGAGATCGAGACCATCCTGGCCAACACAGTGAAACCCCGTCTCCACTAAAATAATACAAA GGTCAGGAGATCGAGACCATCCTGGCCAACACGGTGAAACCCCGTCTCCACTAAAATAATACAAA A G AL807752.1 Ensembl:ENSG00000213590 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982381254 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17437959 37476 RMVar_ID_37476 Human_SNP_ID_418347434 A-to-I Human chr9 - 137039547 137039547 137039547 CCTCTCCTGTTCGGTTTAGACCCCCAAACTGGAGGGGGCATGGAGAACCGTAGAGCGCAGGAACG CCTCTCCTGTTCGGTTTAGACCCCCAAACTGGGGGGGGCATGGAGAACCGTAGAGCGCAGGAACG T C AL807752.6,NPDC1 Ensembl:ENSG00000279073,Ensembl:ENSG00000107281 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006675757 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_715479 37477 RMVar_ID_37477 Human_SNP_ID_418359774 A-to-I Human chr9 + 137076261 137076261 137076261 GCGATCATCCTGTCTCGGTATCCCAAGGTGTTAGGATTACAGGCATGAGCCACTGCACCTGGCCA GCGATCATCCTGTCTCGGTATCCCAAGGTGTTGGGATTACAGGCATGAGCCACTGCACCTGGCCA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1381161649 Functional Loss SNV dbSNP153 33..33 33 - - - 37478 RMVar_ID_37478 Human_SNP_ID_418359775 A-to-I Human chr9 + 137076261 137076261 137076261 GCGATCATCCTGTCTCGGTATCCCAAGGTGTTAGGATTACAGGCATGAGCCACTGCACCTGGCCA GCGATCATCCTGTCTCGGTATCCCAAGGTGTTTGGATTACAGGCATGAGCCACTGCACCTGGCCA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1381161649 Functional Loss SNV dbSNP153 33..33 33 - - - 37479 RMVar_ID_37479 Human_SNP_ID_418376774 A-to-I Human chr9 - 137119625 137119625 137119625 ACCACAGGCTGGACATGGTGGCGCACGCCTGTAATCCCAGCACTTTGGGAGGCCAATGTGGGCGG ACCACAGGCTGGACATGGTGGCGCACGCCTGTGATCCCAGCACTTTGGGAGGCCAATGTGGGCGG T C L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs572366264 Functional Loss SNV dbSNP153 33..33 33 - - - 37480 RMVar_ID_37480 Human_SNP_ID_418376900 A-to-I Human chr9 - 137119998 137119998 137119998 CTGCTTCAGCCTCCCAAGTAGCTGGGACTATAAGCAGCCACCACCACGCCCGGCTAACATATATA CTGCTTCAGCCTCCCAAGTAGCTGGGACTATAGGCAGCCACCACCACGCCCGGCTAACATATATA T C L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1208028791 Functional Loss SNV dbSNP153 33..33 33 - - - 37481 RMVar_ID_37481 Human_SNP_ID_418377190 A-to-I Human chr9 - 137120851 137120851 137120851 AAAATTAGTCGGGCGTGGTGGCGGGCGCTGTAATCCCAACTAAACTCTGGAGGCTGAGGCAGAGA AAAATTAGTCGGGCGTGGTGGCGGGCGCTGTAGTCCCAACTAAACTCTGGAGGCTGAGGCAGAGA T C L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1392013431 Functional Loss SNV dbSNP153 33..33 33 - - - 37482 RMVar_ID_37482 Human_SNP_ID_418380642 A-to-I Human chr9 + 137131958 137131957 137131959 TTTTTATTTATTCACTTATTTTTTTTCGAGACAGAGTCTTCTCTGTCGCTCAGGCTGTAGGTGCA TTTTTATTTATTCACTTATTTTTTTTCGAGAC__AGTCTTCTCTGTCGCTCAGGCTGTAGGTGCA CAG C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1387911067 Functional Loss DEL dbSNP153 33..34 33 - - - 37483 RMVar_ID_37483 Human_SNP_ID_418380656 A-to-I Human chr9 + 137131999 137131999 137131999 TCTGTCGCTCAGGCTGTAGGTGCAGTGGTGCTATCTTGGCTCACTGCAACCTCTGCCTCCTGGAT TCTGTCGCTCAGGCTGTAGGTGCAGTGGTGCTGTCTTGGCTCACTGCAACCTCTGCCTCCTGGAT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs891905416 Functional Loss SNV dbSNP153 33..33 33 - - - 37484 RMVar_ID_37484 Human_SNP_ID_418402847 A-to-I Human chr9 - 137197381 137197381 137197381 GGGACAGAACTGGGCTGGGCGCGGTGGCTCACACCTTGTAATCCCAGCACTTTGGGAGGCCGAGG GGGACAGAACTGGGCTGGGCGCGGTGGCTCACGCCTTGTAATCCCAGCACTTTGGGAGGCCGAGG T C TPRN Ensembl:ENSG00000176058 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1405301355 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_260999,RMVar_hsa_circ_84228 37485 RMVar_ID_37485 Human_SNP_ID_418406559 A-to-I Human chr9 + 137208188 137208188 137208188 AAAAAGAAAAAGAGCCGGGCACTGTGGCTCACACCTGTAATCCTAGCACTTTGGGAGGCCGAGGC AAAAAGAAAAAGAGCCGGGCACTGTGGCTCACGCCTGTAATCCTAGCACTTTGGGAGGCCGAGGC A G NDOR1 Ensembl:ENSG00000188566 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1332329682 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_261002,RMVar_hsa_circ_349705,RMVar_hsa_circ_375153 37486 RMVar_ID_37486 Human_SNP_ID_418406560 A-to-I Human chr9 + 137208188 137208188 137208188 AAAAAGAAAAAGAGCCGGGCACTGTGGCTCACACCTGTAATCCTAGCACTTTGGGAGGCCGAGGC AAAAAGAAAAAGAGCCGGGCACTGTGGCTCACTCCTGTAATCCTAGCACTTTGGGAGGCCGAGGC A T NDOR1 Ensembl:ENSG00000188566 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1332329682 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_261002,RMVar_hsa_circ_349705,RMVar_hsa_circ_375153 37487 RMVar_ID_37487 Human_SNP_ID_418465975 A-to-I Human chr9 - 137377266 137377266 137377266 TTTTGTATTTTTGGTAGAGACGGAGTTCCGCTATGTTGCACAGACTTGTCTTGAACTCCTGAGCT TTTTGTATTTTTGGTAGAGACGGAGTTCCGCTGTGTTGCACAGACTTGTCTTGAACTCCTGAGCT T C EXD3 Ensembl:ENSG00000187609 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs952045999 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1103778 37488 RMVar_ID_37488 Human_SNP_ID_418465998 A-to-I Human chr9 - 137377361 137377361 137377361 AGCTCACTACAACCTCCGCCTCCCGGGTTCAAAGGATTCTCCTGCCTCAGCCTCCCAAGTAGCTG AGCTCACTACAACCTCCGCCTCCCGGGTTCAAGGGATTCTCCTGCCTCAGCCTCCCAAGTAGCTG T C EXD3 Ensembl:ENSG00000187609 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1379635960 Functional Loss SNV dbSNP153 33..33 33 - - - 37489 RMVar_ID_37489 Human_SNP_ID_418466008 A-to-I Human chr9 - 137377398 137377398 137377398 TTCTGTCACCCAGGCTGGAGTGCAATGGCACAATCTCAGCTCACTACAACCTCCGCCTCCCGGGT TTCTGTCACCCAGGCTGGAGTGCAATGGCACAGTCTCAGCTCACTACAACCTCCGCCTCCCGGGT T C EXD3 Ensembl:ENSG00000187609 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1470300629 Functional Loss SNV dbSNP153 33..33 33 - - - 37490 RMVar_ID_37490 Human_SNP_ID_418466009 A-to-I Human chr9 - 137377401 137377401 137377401 TTGTTCTGTCACCCAGGCTGGAGTGCAATGGCACAATCTCAGCTCACTACAACCTCCGCCTCCCG TTGTTCTGTCACCCAGGCTGGAGTGCAATGGCGCAATCTCAGCTCACTACAACCTCCGCCTCCCG T C EXD3 Ensembl:ENSG00000187609 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1256237012 Functional Loss SNV dbSNP153 33..33 33 - - - 37491 RMVar_ID_37491 Human_SNP_ID_418466012 A-to-I Human chr9 - 137377406 137377406 137377406 GAGTCTTGTTCTGTCACCCAGGCTGGAGTGCAATGGCACAATCTCAGCTCACTACAACCTCCGCC GAGTCTTGTTCTGTCACCCAGGCTGGAGTGCAGTGGCACAATCTCAGCTCACTACAACCTCCGCC T C EXD3 Ensembl:ENSG00000187609 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1199215726 Functional Loss SNV dbSNP153 33..33 33 - - - 37492 RMVar_ID_37492 Human_SNP_ID_418468944 A-to-I Human chr9 - 137385632 137385632 137385632 CTACTCCGGAGGCTGAGGCACGAGAATCACGAACCTGAGAGGTGGAGGTTGCAGTGAGCCGAGAT CTACTCCGGAGGCTGAGGCACGAGAATCACGAGCCTGAGAGGTGGAGGTTGCAGTGAGCCGAGAT T C EXD3 Ensembl:ENSG00000187609 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1192473558 Functional Loss SNV dbSNP153 33..33 33 - - - 37493 RMVar_ID_37493 Human_SNP_ID_418471014 A-to-I Human chr9 - 137391973 137391973 137391973 AAAATTAGCTGGACATGGTGGCGGGCGCCTGTATTCCCAGCTACTGGGGAGGCTGAGGCAGGAGA AAAATTAGCTGGACATGGTGGCGGGCGCCTGTGTTCCCAGCTACTGGGGAGGCTGAGGCAGGAGA T C EXD3 Ensembl:ENSG00000187609 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1231882776 Functional Loss SNV dbSNP153 33..33 33 - - - 37494 RMVar_ID_37494 Human_SNP_ID_418508151 A-to-I Human chr9 - 137504507 137504507 137504507 CTGATCTATCTCTTAAATCTGCTTTTCTGGCCAGGAGTGGTGGCTCATGCCTGTAATCCTAGCAC CTGATCTATCTCTTAAATCTGCTTTTCTGGCCCGGAGTGGTGGCTCATGCCTGTAATCCTAGCAC T G PNPLA7 Ensembl:ENSG00000130653 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs531900087 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55214 37495 RMVar_ID_37495 Human_SNP_ID_418523302 A-to-I Human chr9 + 137552426 137552426 137552426 AAGGACGGTACCTTCGACCCTGACAACCTGGAAAAGTACGGCTTCGAGCCCACACAGGAGGGAAA AAGGACGGTACCTTCGACCCTGACAACCTGGAGAAGTACGGCTTCGAGCCCACACAGGAGGGAAA A G MRPL41 Ensembl:ENSG00000182154 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs777898368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5124571,Human_RBP_ID_16621508,Human_RBP_ID_17666941,Human_RBP_ID_27373904 RMVar_hsa_circ_102127,RMVar_hsa_circ_86672,RMVar_hsa_circ_261042,RMVar_hsa_circ_261043 37496 RMVar_ID_37496 Human_SNP_ID_418524658 A-to-I Human chr9 - 137557046 137557044 137557046 AAAACTAGGGGGCATGATGGTCGCAGCTACTCAGGAGGTGAGGCAGGAAGACAGAGCCCAGGTCA AAAACTAGGGGGCATGATGGTCGCAGCTACTC__GAGGTGAGGCAGGAAGACAGAGCCCAGGTCA CCT C DPH7 Ensembl:ENSG00000148399 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1485760344 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_16621604 RMVar_hsa_circ_92687,RMVar_hsa_circ_261044 37497 RMVar_ID_37497 Human_SNP_ID_418524691 A-to-I Human chr9 - 137557177 137557177 137557177 TGTATTGTCTGGGTGCGGTGGCTGACACTCGCAGTCACAGCACTCTGGGAAGGGTGGGCGGATTG TGTATTGTCTGGGTGCGGTGGCTGACACTCGCGGTCACAGCACTCTGGGAAGGGTGGGCGGATTG T C DPH7 Ensembl:ENSG00000148399 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs765941067 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92687,RMVar_hsa_circ_261044 37498 RMVar_ID_37498 Human_SNP_ID_418525177 A-to-I Human chr9 - 137558873 137558873 137558873 GGCGGGCGGATCACCTGAGGTCGGGCGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGTCAGGAGA GGCGGGCGGATCACCTGAGGTCGGGCGCCTGTCGTCCCAGCTACTTGGGAGGCTGAGTCAGGAGA T G DPH7 Ensembl:ENSG00000148399 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs760377482 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16621648 RMVar_hsa_circ_92687,RMVar_hsa_circ_261044 37499 RMVar_ID_37499 Human_SNP_ID_418525978 A-to-I Human chr9 - 137561383 137561383 137561383 GGCACCTGCCACCACGCCTGGCTAATTTTTGTATTTTTATTGGAGACGAGGTTTCACCATGTTGG GGCACCTGCCACCACGCCTGGCTAATTTTTGTGTTTTTATTGGAGACGAGGTTTCACCATGTTGG T C DPH7 Ensembl:ENSG00000148399 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs771230930 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92687,RMVar_hsa_circ_261044 37500 RMVar_ID_37500 Human_SNP_ID_418525999 A-to-I Human chr9 - 137561453 137561453 137561453 CTGCAACCTCCACCTTCCGGGTTCACGCCGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGA CTGCAACCTCCACCTTCCGGGTTCACGCCGCCGTTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGA T C DPH7 Ensembl:ENSG00000148399 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1214320180 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92687,RMVar_hsa_circ_261044 37501 RMVar_ID_37501 Human_SNP_ID_418541008 A-to-I Human chr9 + 137609943 137609943 137609943 TCACGCCATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCGCCCGCCACCACACCCG TCACGCCATTCTCCTGCCTCAGCCTCCTGAGTCGCTGGGACTACAGGCGCCCGCCACCACACCCG A C ARRDC1,AL590627.3 Ensembl:ENSG00000197070,Ensembl:ENSG00000283411 Protein coding,lincRNA intron,intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs555133800 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126454,RMVar_hsa_circ_261050 37502 RMVar_ID_37502 Human_SNP_ID_418541395 A-to-I Human chr9 + 137611293 137611293 137611293 GAGCAGAGCTGGGTACCGTGGCTCATGCCTGTAATCCCAACACTTTGGGAGGCTGAGGCAGGTGG GAGCAGAGCTGGGTACCGTGGCTCATGCCTGTGATCCCAACACTTTGGGAGGCTGAGGCAGGTGG A G ARRDC1,AL590627.3 Ensembl:ENSG00000197070,Ensembl:ENSG00000283411 Protein coding,lincRNA intron,intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1025980197 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126454,RMVar_hsa_circ_261050 37503 RMVar_ID_37503 Human_SNP_ID_418541404 A-to-I Human chr9 + 137611320 137611320 137611320 CCTGTAATCCCAACACTTTGGGAGGCTGAGGCAGGTGGATTGCTTGAGCTTAGGAGTTTGAGACC CCTGTAATCCCAACACTTTGGGAGGCTGAGGCGGGTGGATTGCTTGAGCTTAGGAGTTTGAGACC A G ARRDC1,AL590627.3 Ensembl:ENSG00000197070,Ensembl:ENSG00000283411 Protein coding,lincRNA intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs969974762 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126454,RMVar_hsa_circ_261050 37504 RMVar_ID_37504 Human_SNP_ID_418541443 A-to-I Human chr9 + 137611438 137611438 137611438 AACAAAACCCAGGTGTGGTGGCACGTGCCTGTAGTCCTAGCTACTTGCGGGGCTGAGATGGGTGG AACAAAACCCAGGTGTGGTGGCACGTGCCTGTCGTCCTAGCTACTTGCGGGGCTGAGATGGGTGG A C ARRDC1,AL590627.3 Ensembl:ENSG00000197070,Ensembl:ENSG00000283411 Protein coding,lincRNA intron,intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1051667433 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126454,RMVar_hsa_circ_261050 37505 RMVar_ID_37505 Human_SNP_ID_418541444 A-to-I Human chr9 + 137611438 137611438 137611438 AACAAAACCCAGGTGTGGTGGCACGTGCCTGTAGTCCTAGCTACTTGCGGGGCTGAGATGGGTGG AACAAAACCCAGGTGTGGTGGCACGTGCCTGTGGTCCTAGCTACTTGCGGGGCTGAGATGGGTGG A G ARRDC1,AL590627.3 Ensembl:ENSG00000197070,Ensembl:ENSG00000283411 Protein coding,lincRNA intron,intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1051667433 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126454,RMVar_hsa_circ_261050 37506 RMVar_ID_37506 Human_SNP_ID_418541463 A-to-I Human chr9 + 137611492 137611492 137611492 GAGATGGGTGGATCGCTTGAACACAGGAGGTTAAGGCTGCAGTGAGCCGAGATCGTGCCACTGCA GAGATGGGTGGATCGCTTGAACACAGGAGGTTGAGGCTGCAGTGAGCCGAGATCGTGCCACTGCA A G ARRDC1,AL590627.3 Ensembl:ENSG00000197070,Ensembl:ENSG00000283411 Protein coding,lincRNA intron,intron GSE38233;GSE100210;GSE100210;GSE107867 cultured B-cells;HepG2 cell line;HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 24183664,29129909,29129909,30559470 RNA-Seq:(High) rs1449843993 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126454,RMVar_hsa_circ_261050 37507 RMVar_ID_37507 Human_SNP_ID_418541464 A-to-I Human chr9 - 137611502 137611502 137611502 CAGGCTAGTGTGCAGTGGCACGATCTCGGCTCACTGCAGCCTTAACCTCCTGTGTTCAAGCGATC CAGGCTAGTGTGCAGTGGCACGATCTCGGCTCGCTGCAGCCTTAACCTCCTGTGTTCAAGCGATC T C lnc-ZMYND19-2,lnc-ZMYND19-2:2 RNACentral:URS00008C11BA,RNACentral:URS00009BED5A lincRNA,lincRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1010584182 Functional Loss SNV dbSNP153 33..33 33 - - - 37508 RMVar_ID_37508 Human_SNP_ID_418541949 A-to-I Human chr9 - 137612876 137612876 137612876 GTCACCCGGATGGCTGCAAAGGGGATGGCTGCATGAGCCCCAGCCAGCCGACGGCCCAGGCCCCT GTCACCCGGATGGCTGCAAAGGGGATGGCTGCGTGAGCCCCAGCCAGCCGACGGCCCAGGCCCCT T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs779219569 Functional Loss SNV dbSNP153 33..33 33 - - - 37509 RMVar_ID_37509 Human_SNP_ID_418543461 A-to-I Human chr9 - 137616121 137616121 137616121 CAAGCAATCCACCTGCCTCAGCCTCCCAAAGTACTGGGATTACAGGAGGGAGCCACCGTGCCCGG CAAGCAATCCACCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGAGGGAGCCACCGTGCCCGG T C ARRDC1-AS1 Ensembl:ENSG00000203993 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1193352955 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5041722 Human_Splice_Rec_1104562,Human_Splice_Rec_1104564,Human_Splice_Rec_1104566 37510 RMVar_ID_37510 Human_SNP_ID_418543467 A-to-I Human chr9 - 137616134 137616134 137616134 GAACTCCTGACCTCAAGCAATCCACCTGCCTCAGCCTCCCAAAGTACTGGGATTACAGGAGGGAG GAACTCCTGACCTCAAGCAATCCACCTGCCTCGGCCTCCCAAAGTACTGGGATTACAGGAGGGAG T C ARRDC1-AS1 Ensembl:ENSG00000203993 lincRNA exon GSE56152;GSE100210 embryonic stem cells,wild type;HepG2 cell line - 25708366,29129909 RNA-Seq:(High) rs1391511211 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1104562,Human_Splice_Rec_1104564 37511 RMVar_ID_37511 Human_SNP_ID_418543555 A-to-I Human chr9 - 137616289 137616289 137616289 TCACTGTAACCTCTGCCACCTGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAATTGGGA TCACTGTAACCTCTGCCACCTGGGTTCAAGCGGTTCTCCTGCCTCAGCCTCCTGAGTAATTGGGA T C ARRDC1-AS1 Ensembl:ENSG00000203993 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs932683292 Functional Loss SNV dbSNP153 33..33 33 - - - 37512 RMVar_ID_37512 Human_SNP_ID_418543802 A-to-I Human chr9 - 137617189 137617189 137617189 GAATGGCATGAACCCGGGAGGCAGAGCTTGCAATGAGCTGAGATTGTGCCACTGCACTCCAGCCT GAATGGCATGAACCCGGGAGGCAGAGCTTGCAGTGAGCTGAGATTGTGCCACTGCACTCCAGCCT T C ARRDC1-AS1 Ensembl:ENSG00000203993 lincRNA intron GSE99789;GSE123020:GSM3490829,GSM3490830,GSM3490831 esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109 cell line - 29796672,32596459 RNA-Seq:(High) rs1485808753 Functional Loss SNV dbSNP153 33..33 33 - - - 37513 RMVar_ID_37513 Human_SNP_ID_418543838 A-to-I Human chr9 + 137617319 137617319 137617319 TATTTTTAGTAGAGATGGGGTTTCACCATGTTAGCCAGGCTGGTCTCCATCTCCTGACCTCATGA TATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTCCATCTCCTGACCTCATGA A G AL590627.3 Ensembl:ENSG00000283411 lincRNA intron GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1434139933 Functional Loss SNV dbSNP153 33..33 33 - - - 37514 RMVar_ID_37514 Human_SNP_ID_418544961 A-to-I Human chr9 + 137620509 137620509 137620509 ATGATCACTGCTCACTGCAGCTTCGACCACCCAGGCTCAAAGGAGTCTCCCACCTCGGGTGCTGC ATGATCACTGCTCACTGCAGCTTCGACCACCCGGGCTCAAAGGAGTCTCCCACCTCGGGTGCTGC A G AL590627.3,EHMT1 Ensembl:ENSG00000283411,Ensembl:ENSG00000181090 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs564960513 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16622851 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 37515 RMVar_ID_37515 Human_SNP_ID_418545956 A-to-I Human chr9 + 137623886 137623886 137623886 TTTGAGACAGTCTGGAGGAGTGGTTCAATGATAGTTCTCTGCAGCCTTGACCTCCCGGGCTGAAG TTTGAGACAGTCTGGAGGAGTGGTTCAATGATGGTTCTCTGCAGCCTTGACCTCCCGGGCTGAAG A G AL590627.3,EHMT1 Ensembl:ENSG00000283411,Ensembl:ENSG00000181090 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1351281576 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16622941 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 37516 RMVar_ID_37516 Human_SNP_ID_418548176 A-to-I Human chr9 + 137631767 137631767 137631767 GGGCATTGTGGTGTGTGCCTGTAGACCCAGCTACTCCGGGAGGCTGAGGTGGGGAGAGTTGTTTG GGGCATTGTGGTGTGTGCCTGTAGACCCAGCTGCTCCGGGAGGCTGAGGTGGGGAGAGTTGTTTG A G AL590627.3,EHMT1 Ensembl:ENSG00000283411,Ensembl:ENSG00000181090 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909301580 Functional Loss SNV dbSNP153 33..33 33 - - - 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 37517 RMVar_ID_37517 Human_SNP_ID_418553684 A-to-I Human chr9 + 137650952 137650952 137650952 ATATGAATATGTGCACACCCGTGGTTCCAGCTACTCAGGAGGCTGAGGTGGGAGGATCACGAGCC ATATGAATATGTGCACACCCGTGGTTCCAGCTTCTCAGGAGGCTGAGGTGGGAGGATCACGAGCC A T AL590627.3,EHMT1 Ensembl:ENSG00000283411,Ensembl:ENSG00000181090 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1299034412 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1104628,Human_Splice_Rec_1104629 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 37518 RMVar_ID_37518 Human_SNP_ID_418564815 A-to-I Human chr9 + 137690569 137690565 137690570 AGATGTCGAAGAATATATCTTGTTTCTTGTTTATTTTATTTTATTTTTTTTGAGACAGAGTCTTG AGATGTCGAAGAATATATCTTGTTTCTTG_____TTTATTTTATTTTTTTTGAGACAGAGTCTTG GTTTAT G AL590627.3,EHMT1 Ensembl:ENSG00000283411,Ensembl:ENSG00000181090 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1458269119 Functional Loss DEL dbSNP153 30..34 33 - - - Human_RBP_ID_182353 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 37519 RMVar_ID_37519 Human_SNP_ID_418599268 A-to-I Human chr9 + 137808855 137808855 137808855 TAAGGCACGAGAATCGCTTGAACCCCAGAGGCAGAGGTTGCAGTGAACCAAGATCGTGCCAACTG TAAGGCACGAGAATCGCTTGAACCCCAGAGGCGGAGGTTGCAGTGAACCAAGATCGTGCCAACTG A G EHMT1 Ensembl:ENSG00000181090 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1333268340 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103423,RMVar_hsa_circ_318929,RMVar_hsa_circ_261062,RMVar_hsa_circ_72224,RMVar_hsa_circ_261073,RMVar_hsa_circ_313864,RMVar_hsa_circ_261085,RMVar_hsa_circ_360394,RMVar_hsa_circ_83777,RMVar_hsa_circ_261086,RMVar_hsa_circ_332958,RMVar_hsa_circ_261097,RMVar_hsa_circ_41490,RMVar_hsa_circ_99787,RMVar_hsa_circ_285558,RMVar_hsa_circ_71271,RMVar_hsa_circ_104125,RMVar_hsa_circ_261106,RMVar_hsa_circ_261107,RMVar_hsa_circ_261105,RMVar_hsa_circ_261110,RMVar_hsa_circ_88014,RMVar_hsa_circ_75840,RMVar_hsa_circ_261108,RMVar_hsa_circ_261109,RMVar_hsa_circ_98690,RMVar_hsa_circ_268157,RMVar_hsa_circ_261113,RMVar_hsa_circ_97305,RMVar_hsa_circ_20733,RMVar_hsa_circ_64910,RMVar_hsa_circ_18544,RMVar_hsa_circ_32165,RMVar_hsa_circ_261117,RMVar_hsa_circ_287585,RMVar_hsa_circ_261120,RMVar_hsa_circ_345967,RMVar_hsa_circ_25836,RMVar_hsa_circ_43494,RMVar_hsa_circ_125784,RMVar_hsa_circ_261124 37520 RMVar_ID_37520 Human_SNP_ID_418603478 A-to-I Human chr9 + 137821467 137821467 137821467 TTCCTGCCTTGACCTCCCAAGTAGGTAGGACTACAAGTGTGCACTACAATGCCCGGCTAATTTTT TTCCTGCCTTGACCTCCCAAGTAGGTAGGACTGCAAGTGTGCACTACAATGCCCGGCTAATTTTT A G EHMT1 Ensembl:ENSG00000181090 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1341662200 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16626141 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 37521 RMVar_ID_37521 Human_SNP_ID_305194306 A-to-I Human chr6 - 165531250 165531250 165531250 TATAATGGAGCTTTGAATCTAAATGGGGCAAAAATAGTAAGCAACCAATTAGACCATAAATATAA TATAATGGAGCTTTGAATCTAAATGGGGCAAAGATAGTAAGCAACCAATTAGACCATAAATATAA T C PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs964949387 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10778,RMVar_hsa_circ_314895,RMVar_hsa_circ_285082,RMVar_hsa_circ_13103,RMVar_hsa_circ_66821,RMVar_hsa_circ_290929,RMVar_hsa_circ_33457,RMVar_hsa_circ_295055,RMVar_hsa_circ_346413,RMVar_hsa_circ_242948,RMVar_hsa_circ_242950,RMVar_hsa_circ_331221,RMVar_hsa_circ_373920,RMVar_hsa_circ_242949 37522 RMVar_ID_37522 Human_SNP_ID_305263789 A-to-I Human chr6 - 165795469 165795469 165795469 TGCCCACCTCAGCCTCCCAAATTGCTGGGACTACAGGTATGAGCCACCGCGCCCAGCCCTTGACC TGCCCACCTCAGCCTCCCAAATTGCTGGGACTGCAGGTATGAGCCACCGCGCCCAGCCCTTGACC T C PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005214197 Functional Loss SNV dbSNP153 33..33 33 - - - 37523 RMVar_ID_37523 Human_SNP_ID_305265238 A-to-I Human chr6 - 165801410 165801410 165801410 CTCCCAAGTAGCTGGAATTACAGGCATGTACCACCATGCCTTGCTAATTTTTGTGTTTTTAGCAG CTCCCAAGTAGCTGGAATTACAGGCATGTACCGCCATGCCTTGCTAATTTTTGTGTTTTTAGCAG T C PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1359865122 Functional Loss SNV dbSNP153 33..33 33 - - - 37524 RMVar_ID_37524 Human_SNP_ID_305281112 A-to-I Human chr6 - 165862609 165862606 165862610 TCTTTGACTCACTTGCTCTTAGTGCACCTGTTAGTGTGGTCCTGAATTCATCAGGATTCTATTTA TCTTTGACTCACTTGCTCTTAGTGCACCTGT____GTGGTCCTGAATTCATCAGGATTCTATTTA CACTA C PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1228069109 Functional Loss DEL dbSNP153 32..35 33 - - - 37525 RMVar_ID_37525 Human_SNP_ID_305285608 A-to-I Human chr6 - 165881498 165881498 165881498 GCTAATCCTCAGGAGGCTGAGGCAGGAGAATCACCTGAACCCAGGAGGGGGAGATTGCAGTGAGC GCTAATCCTCAGGAGGCTGAGGCAGGAGAATCTCCTGAACCCAGGAGGGGGAGATTGCAGTGAGC T A PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1453033456 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8636819 37526 RMVar_ID_37526 Human_SNP_ID_305285611 A-to-I Human chr6 - 165881511 165881506 165881511 ACCTGTAGTCCCAGCTAATCCTCAGGAGGCTGAGGCAGGAGAATCACCTGAACCCAGGAGGGGGA ACCTGTAGTCCCAGCTAATCCTCAGGAGGCTG_____GGAGAATCACCTGAACCCAGGAGGGGGA CTGCCT C PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1242080828 Functional Loss DEL dbSNP153 33..37 33 - - - 37527 RMVar_ID_37527 Human_SNP_ID_305285621 A-to-I Human chr6 - 165881537 165881537 165881537 AAAATTAGCTGGGCATGGTGGTGCGCACCTGTAGTCCCAGCTAATCCTCAGGAGGCTGAGGCAGG AAAATTAGCTGGGCATGGTGGTGCGCACCTGTGGTCCCAGCTAATCCTCAGGAGGCTGAGGCAGG T C PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1374202060 Functional Loss SNV dbSNP153 33..33 33 - - - 37528 RMVar_ID_37528 Human_SNP_ID_305286005 A-to-I Human chr6 - 165883043 165883043 165883043 TTAGTAGAGATGGGGTTTCACCATTTTGGCCAAGCTGGTCTCAAACTCCTGACCTCGAGCAATCT TTAGTAGAGATGGGGTTTCACCATTTTGGCCACGCTGGTCTCAAACTCCTGACCTCGAGCAATCT T G PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1475821199 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15728084 37529 RMVar_ID_37529 Human_SNP_ID_305289748 A-to-I Human chr6 - 165897417 165897417 165897417 CCCTGGGACCCTCCCTATCTCCCCCACCCCCAAATACTGGATGGTGCCCACTCCCAGACTGTCCT CCCTGGGACCCTCCCTATCTCCCCCACCCCCAGATACTGGATGGTGCCCACTCCCAGACTGTCCT T C PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1221717077 Functional Loss SNV dbSNP153 33..33 33 - - - 37530 RMVar_ID_37530 Human_SNP_ID_305289754 A-to-I Human chr6 - 165897457 165897457 165897457 CCCTGGGGGCACCTGCAGCTCAGGACCCTCTCATTCTCCTCCCTGGGACCCTCCCTATCTCCCCC CCCTGGGGGCACCTGCAGCTCAGGACCCTCTCTTTCTCCTCCCTGGGACCCTCCCTATCTCCCCC T A PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270640234 Functional Loss SNV dbSNP153 33..33 33 - - - 37531 RMVar_ID_37531 Human_SNP_ID_305289833 A-to-I Human chr6 - 165897691 165897691 165897691 CCAGGATTCCCAGAGGACACGTCGGAACTCCAAGATGAACAGGTCACTCCAGGGCAGGAAGCAAA CCAGGATTCCCAGAGGACACGTCGGAACTCCAGGATGAACAGGTCACTCCAGGGCAGGAAGCAAA T C PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924590732 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15728248 37532 RMVar_ID_37532 Human_SNP_ID_305290361 A-to-I Human chr6 - 165899812 165899812 165899812 ACCAAGAAGGTGGCTGCAGTTGATTCTGTAGCAACTCCCAGGAGAGCAGAGCTCTGCCTTAGCCA ACCAAGAAGGTGGCTGCAGTTGATTCTGTAGCGACTCCCAGGAGAGCAGAGCTCTGCCTTAGCCA T C PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1197681256 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15728275 37533 RMVar_ID_37533 Human_SNP_ID_305290368 A-to-I Human chr6 - 165899837 165899835 165899838 AAGCAGAGGGAGATGCTATTTTTACACCAAGAAGGTGGCTGCAGTTGATTCTGTAGCAACTCCCA AAGCAGAGGGAGATGCTATTTTTACACCAAG___GTGGCTGCAGTTGATTCTGTAGCAACTCCCA CCTT C PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1562789153 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_2991545 37534 RMVar_ID_37534 Human_SNP_ID_305290370 A-to-I Human chr6 - 165899837 165899837 165899837 AAGCAGAGGGAGATGCTATTTTTACACCAAGAAGGTGGCTGCAGTTGATTCTGTAGCAACTCCCA AAGCAGAGGGAGATGCTATTTTTACACCAAGACGGTGGCTGCAGTTGATTCTGTAGCAACTCCCA T G PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1050393812 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2991545 37535 RMVar_ID_37535 Human_SNP_ID_305290488 A-to-I Human chr6 - 165900344 165900344 165900344 CCTCAGCCTCTGGAGTAGCTGGGATTACTGGCACCTGACATCATGCCCAGCTAATTTTTGTATTT CCTCAGCCTCTGGAGTAGCTGGGATTACTGGCGCCTGACATCATGCCCAGCTAATTTTTGTATTT T C PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1295935568 Functional Loss SNV dbSNP153 33..33 33 - - - 37536 RMVar_ID_37536 Human_SNP_ID_305290859 A-to-I Human chr6 - 165901637 165901637 165901637 CCACCATGCGTGGCTAATTTTGTATTTTTAGTAGAGACAGAGTTTCTCCGTGTTGGTCAGGCTGG CCACCATGCGTGGCTAATTTTGTATTTTTAGTGGAGACAGAGTTTCTCCGTGTTGGTCAGGCTGG T C PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1244639255 Functional Loss SNV dbSNP153 33..33 33 - - - 37537 RMVar_ID_37537 Human_SNP_ID_305302091 A-to-I Human chr6 - 165943988 165943988 165943988 TGAGTCAATTAAACCTATTTCCTTTATAAATTACCCAGTCTTGGGTATGTCTTTATCAGCAGTGT TGAGTCAATTAAACCTATTTCCTTTATAAATTCCCCAGTCTTGGGTATGTCTTTATCAGCAGTGT T G PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs993359659 Functional Loss SNV dbSNP153 33..33 33 - - - 37538 RMVar_ID_37538 Human_SNP_ID_305403481 A-to-I Human chr6 - 166320655 166320655 166320655 AAAAAAAAAATTAGTGTAGTGGTGTGCCCTATAGTCCCAGCTCCTTGGGAGGCTGAGGTGGGAGG AAAAAAAAAATTAGTGTAGTGGTGTGCCCTATCGTCCCAGCTCCTTGGGAGGCTGAGGTGGGAGG T G SFT2D1 Ensembl:ENSG00000198818 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs995496038 Functional Loss SNV dbSNP153 33..33 33 - - - 37539 RMVar_ID_37539 Human_SNP_ID_305403534 A-to-I Human chr6 - 166320789 166320789 166320789 CTTTGGGCTGGGCTTGGTGGCTCATCCCTGTAATCCCAGCATTTTGGGAGGCTGAGACGGGTGGA CTTTGGGCTGGGCTTGGTGGCTCATCCCTGTAGTCCCAGCATTTTGGGAGGCTGAGACGGGTGGA T C SFT2D1 Ensembl:ENSG00000198818 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1179758745 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15922487 37540 RMVar_ID_37540 Human_SNP_ID_305403590 A-to-I Human chr6 - 166321028 166321028 166321028 CTGCTCACTGCAACCTCCACCTCCCAAGTTCAAGAGTTTCTCCTGGCTCAGCCTCCTGAGTAGCT CTGCTCACTGCAACCTCCACCTCCCAAGTTCAGGAGTTTCTCCTGGCTCAGCCTCCTGAGTAGCT T C SFT2D1 Ensembl:ENSG00000198818 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1404410822 Functional Loss SNV dbSNP153 33..33 33 - - - 37541 RMVar_ID_37541 Human_SNP_ID_305403608 A-to-I Human chr6 - 166321072 166321072 166321072 GAGTCTCATTTTGTCACCCAGGCTGGAGTACAATGGCGTGATCTCTGCTCACTGCAACCTCCACC GAGTCTCATTTTGTCACCCAGGCTGGAGTACAGTGGCGTGATCTCTGCTCACTGCAACCTCCACC T C SFT2D1 Ensembl:ENSG00000198818 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs535824718 Functional Loss SNV dbSNP153 33..33 33 - - - 37542 RMVar_ID_37542 Human_SNP_ID_305403952 A-to-I Human chr6 - 166322524 166322524 166322524 CATGCCCGGCTAATTTTTTTGTGTATTTTAGTAGAGACGGGATTTCACCATGTTGGCCAGGATGG CATGCCCGGCTAATTTTTTTGTGTATTTTAGTGGAGACGGGATTTCACCATGTTGGCCAGGATGG T C SFT2D1 Ensembl:ENSG00000198818 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1445880715 Functional Loss SNV dbSNP153 33..33 33 - - - 37543 RMVar_ID_37543 Human_SNP_ID_305405757 A-to-I Human chr6 - 166329535 166329535 166329535 CGGGCGGCATAAAGCTTTTTGCAGTGTTTTATACCCTCGGCAATCTTGCTGCGTTAGCCAGGTAC CGGGCGGCATAAAGCTTTTTGCAGTGTTTTATGCCCTCGGCAATCTTGCTGCGTTAGCCAGGTAC T C SFT2D1 Ensembl:ENSG00000198818 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1562444040 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_657113,Human_RBP_ID_7572686,Human_RBP_ID_9350350,Human_RBP_ID_17709933,Human_RBP_ID_22619517,Human_RBP_ID_24147228,Human_RBP_ID_24511501,Human_RBP_ID_26828953 Human_Splice_Rec_832440,Human_Splice_Rec_832441,Human_Splice_Rec_832456,Human_Splice_Rec_832457,Human_Splice_Rec_832472,Human_Splice_Rec_832473,Human_Splice_Rec_832486,Human_Splice_Rec_832487 RMVar_hsa_circ_282870,RMVar_hsa_circ_337042 37544 RMVar_ID_37544 Human_SNP_ID_305406453 A-to-I Human chr6 - 166332393 166332393 166332393 AAAATTAGTCAGGCCTGGTGGCGTGGACCTGTAGTCCCAGCTAATTGGGAGACTGAGGTAGGAGA AAAATTAGTCAGGCCTGGTGGCGTGGACCTGTGGTCCCAGCTAATTGGGAGACTGAGGTAGGAGA T C SFT2D1 Ensembl:ENSG00000198818 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs574926486 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22617658 37545 RMVar_ID_37545 Human_SNP_ID_305407003 A-to-I Human chr6 - 166334511 166334511 166334511 TCGGCTCACTGCAACCTCTGACTCCCGGGCTCAGGTGATCCTCCCACCTCGGCCTCCCAAGTAGC TCGGCTCACTGCAACCTCTGACTCCCGGGCTCGGGTGATCCTCCCACCTCGGCCTCCCAAGTAGC T C SFT2D1 Ensembl:ENSG00000198818 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1325162876 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_252472 37546 RMVar_ID_37546 Human_SNP_ID_305473052 A-to-I Human chr6 + 166593296 166593296 166593296 ATACAACAGAACAAAATAGAATAGAATGAAATAGAAGAGAATGGAATGGAATGGAATAGAATAAA ATACAACAGAACAAAATAGAATAGAATGAAATGGAAGAGAATGGAATGGAATGGAATAGAATAAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1050921527 Functional Loss SNV dbSNP153 33..33 33 - - - 37547 RMVar_ID_37547 Human_SNP_ID_305500149 A-to-I Human chr6 - 166702118 166702118 166702118 TCTAAAATCGATGTCCACCGTAAAGAAAATGCAGGGGCTGCTGAGAAGTCGATTACTATCCTCTC TCTAAAATCGATGTCCACCGTAAAGAAAATGCGGGGGCTGCTGAGAAGTCGATTACTATCCTCTC T C RPS6KA2,AL023775.1 Ensembl:ENSG00000071242,Ensembl:ENSG00000235008 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs905067196 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_168929,Human_RBP_ID_17422636 RMVar_hsa_circ_128112,RMVar_hsa_circ_242972,RMVar_hsa_circ_80982,RMVar_hsa_circ_242975 37548 RMVar_ID_37548 Human_SNP_ID_305561675 A-to-I Human chr6 - 166939294 166939294 166939294 TGGAGTTTGTCTCTTGCCCAGGCTATAGTGCAATGGCATGATCTTGGCTCACTGCAACCTCTGCC TGGAGTTTGTCTCTTGCCCAGGCTATAGTGCAGTGGCATGATCTTGGCTCACTGCAACCTCTGCC T C AL159163.1,RNASET2 Ensembl:ENSG00000249141,Ensembl:ENSG00000026297 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1301730814 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6188,RMVar_hsa_circ_342127,RMVar_hsa_circ_242981,RMVar_hsa_circ_308022,RMVar_hsa_circ_365535,RMVar_hsa_circ_242977,RMVar_hsa_circ_317145,RMVar_hsa_circ_302598,RMVar_hsa_circ_365957,RMVar_hsa_circ_242980,RMVar_hsa_circ_333448,RMVar_hsa_circ_242982 37549 RMVar_ID_37549 Human_SNP_ID_305562341 A-to-I Human chr6 - 166942332 166942332 166942332 TAAGAAAAAAGAGACCAGGCACAGTGGTTCACACCTGTAATCCCAGCACTTTGGAAGGCCAAGGC TAAGAAAAAAGAGACCAGGCACAGTGGTTCACGCCTGTAATCCCAGCACTTTGGAAGGCCAAGGC T C AL159163.1,RNASET2 Ensembl:ENSG00000249141,Ensembl:ENSG00000026297 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1035689683 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_169031 RMVar_hsa_circ_6188,RMVar_hsa_circ_342127,RMVar_hsa_circ_242981,RMVar_hsa_circ_308022,RMVar_hsa_circ_365535,RMVar_hsa_circ_242977,RMVar_hsa_circ_317145,RMVar_hsa_circ_302598,RMVar_hsa_circ_365957,RMVar_hsa_circ_242980,RMVar_hsa_circ_333448,RMVar_hsa_circ_242982 37550 RMVar_ID_37550 Human_SNP_ID_305562345 A-to-I Human chr6 - 166942348 166942348 166942348 CTGTCTTCAAATACATTAAGAAAAAAGAGACCAGGCACAGTGGTTCACACCTGTAATCCCAGCAC CTGTCTTCAAATACATTAAGAAAAAAGAGACCGGGCACAGTGGTTCACACCTGTAATCCCAGCAC T C AL159163.1,RNASET2 Ensembl:ENSG00000249141,Ensembl:ENSG00000026297 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs558378190 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_169031 RMVar_hsa_circ_6188,RMVar_hsa_circ_342127,RMVar_hsa_circ_242981,RMVar_hsa_circ_308022,RMVar_hsa_circ_365535,RMVar_hsa_circ_242977,RMVar_hsa_circ_317145,RMVar_hsa_circ_302598,RMVar_hsa_circ_365957,RMVar_hsa_circ_242980,RMVar_hsa_circ_333448,RMVar_hsa_circ_242982 37551 RMVar_ID_37551 Human_SNP_ID_305573789 A-to-I Human chr6 - 166982385 166982385 166982385 AGAGTGAAACTCCGTCTCAAAAAAAAAAAAAAAAAAAAGAAAATCAAAAGGAATAGATCCAAACA AGAGTGAAACTCCGTCTCAAAAAAAAAAAAAAGAAAAAGAAAATCAAAAGGAATAGATCCAAACA T C Z94721.1 Ensembl:ENSG00000227598 lincRNA intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs370876914 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_4170,GWAS_ID_4171,GWAS_ID_4172,GWAS_ID_4173,GWAS_ID_4174,GWAS_ID_4175,GWAS_ID_4176,GWAS_ID_4177,GWAS_ID_4178,GWAS_ID_4179,GWAS_ID_4180,GWAS_ID_4181,GWAS_ID_4182,GWAS_ID_4183,GWAS_ID_4184,GWAS_ID_4185,GWAS_ID_4186,GWAS_ID_4187,GWAS_ID_4188,GWAS_ID_4189,GWAS_ID_4190,GWAS_ID_4191,GWAS_ID_4192,GWAS_ID_4193,GWAS_ID_4194,GWAS_ID_4195,GWAS_ID_4196,GWAS_ID_4197,GWAS_ID_4198,GWAS_ID_4199,GWAS_ID_4200,GWAS_ID_4201,GWAS_ID_4202,GWAS_ID_4203,GWAS_ID_4204,GWAS_ID_4205,GWAS_ID_4206,GWAS_ID_4207,GWAS_ID_4208,GWAS_ID_4209,GWAS_ID_4210,GWAS_ID_4211,GWAS_ID_4212,GWAS_ID_4213,GWAS_ID_4214,GWAS_ID_4215,GWAS_ID_4216,GWAS_ID_4217,GWAS_ID_4218,GWAS_ID_4219,GWAS_ID_4220,GWAS_ID_4221,GWAS_ID_4222,GWAS_ID_4223,GWAS_ID_4224,GWAS_ID_4225,GWAS_ID_4226,GWAS_ID_4227,GWAS_ID_4228,GWAS_ID_4229,GWAS_ID_4230,GWAS_ID_4231,GWAS_ID_4232,GWAS_ID_4233,GWAS_ID_4234,GWAS_ID_4235,GWAS_ID_4236,GWAS_ID_4237,GWAS_ID_4238,GWAS_ID_4239,GWAS_ID_4240,GWAS_ID_4241,GWAS_ID_4242,GWAS_ID_4243,GWAS_ID_4244,GWAS_ID_4245,GWAS_ID_4246,GWAS_ID_4247,GWAS_ID_4248,GWAS_ID_4249,GWAS_ID_4250,GWAS_ID_4251,GWAS_ID_4252,GWAS_ID_4253,GWAS_ID_4254,GWAS_ID_4255,GWAS_ID_4256,GWAS_ID_4257,GWAS_ID_4258,GWAS_ID_4259,GWAS_ID_4260,GWAS_ID_4261,GWAS_ID_4262,GWAS_ID_4263,GWAS_ID_4264,GWAS_ID_4265,GWAS_ID_4266,GWAS_ID_4267,GWAS_ID_4268,GWAS_ID_4269,GWAS_ID_4270,GWAS_ID_4271,GWAS_ID_4272,GWAS_ID_4273,GWAS_ID_4274,GWAS_ID_4275,GWAS_ID_4276,GWAS_ID_4277,GWAS_ID_4278,GWAS_ID_4279,GWAS_ID_4280,GWAS_ID_4281,GWAS_ID_4282,GWAS_ID_4283,GWAS_ID_4284,GWAS_ID_4285,GWAS_ID_4286,GWAS_ID_4287,GWAS_ID_4288,GWAS_ID_4289,GWAS_ID_4290,GWAS_ID_4291,GWAS_ID_4292,GWAS_ID_4293,GWAS_ID_4294,GWAS_ID_4295,GWAS_ID_4296,GWAS_ID_4297,GWAS_ID_4298,GWAS_ID_4299,GWAS_ID_4300,GWAS_ID_4301,GWAS_ID_4302,GWAS_ID_4303,GWAS_ID_4304,GWAS_ID_4305,GWAS_ID_4306,GWAS_ID_4307,GWAS_ID_4308,GWAS_ID_4309,GWAS_ID_4310,GWAS_ID_4311,GWAS_ID_4312,GWAS_ID_4313,GWAS_ID_4314,GWAS_ID_4315,GWAS_ID_4316,GWAS_ID_4317,GWAS_ID_4318,GWAS_ID_4319 37552 RMVar_ID_37552 Human_SNP_ID_305580752 A-to-I Human chr6 + 167008977 167008977 167008977 AGTAAGAATAGAAATAAGTGGACATACAGGCTAGACATGGTGGCTCACACCTGTAATTCCAGCAC AGTAAGAATAGAAATAAGTGGACATACAGGCTGGACATGGTGGCTCACACCTGTAATTCCAGCAC A G Z94721.2,FGFR1OP Ensembl:ENSG00000272980,Ensembl:ENSG00000213066 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167394525 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5251008,Human_RBP_ID_15735167 RMVar_hsa_circ_9158,RMVar_hsa_circ_36990,RMVar_hsa_circ_58227,RMVar_hsa_circ_356145,RMVar_hsa_circ_31414 37553 RMVar_ID_37553 Human_SNP_ID_305580995 A-to-I Human chr6 + 167009614 167009614 167009614 TTGAACCCGGCAGTCGGAGGTTGCAGTAAGCCAAGATCTCGCCATTGCACTCTAACCTGGACAAC TTGAACCCGGCAGTCGGAGGTTGCAGTAAGCCGAGATCTCGCCATTGCACTCTAACCTGGACAAC A G Z94721.2,FGFR1OP Ensembl:ENSG00000272980,Ensembl:ENSG00000213066 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs962064353 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1216127,Human_RBP_ID_15735177 RMVar_hsa_circ_9158,RMVar_hsa_circ_36990,RMVar_hsa_circ_58227,RMVar_hsa_circ_356145,RMVar_hsa_circ_31414 37554 RMVar_ID_37554 Human_SNP_ID_305583023 A-to-I Human chr6 + 167017202 167017198 167017202 TATTTTTAGTAGAGACGGGGTTTCACTGTGTTAGCTAGGATGGTCTTGATCTCCTGACCTCGTGA TATTTTTAGTAGAGACGGGGTTTCACTGT____GCTAGGATGGTCTTGATCTCCTGACCTCGTGA TGTTA T Z94721.2,FGFR1OP Ensembl:ENSG00000272980,Ensembl:ENSG00000213066 lincRNA,Protein coding intron,intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1358266722 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_36990,RMVar_hsa_circ_58227,RMVar_hsa_circ_31414,RMVar_hsa_circ_242985,RMVar_hsa_circ_242987,RMVar_hsa_circ_283437,RMVar_hsa_circ_299152,RMVar_hsa_circ_331352,RMVar_hsa_circ_242988,RMVar_hsa_circ_242986 37555 RMVar_ID_37555 Human_SNP_ID_305586101 A-to-I Human chr6 + 167029195 167029195 167029195 AAGAATGAAAGTAAGGAAAGCAGAAGGCTGTCAGGAAGTCCGGGCCAAAGATGACTGGGGTAAGG AAGAATGAAAGTAAGGAAAGCAGAAGGCTGTCGGGAAGTCCGGGCCAAAGATGACTGGGGTAAGG A G Z94721.2,FGFR1OP Ensembl:ENSG00000272980,Ensembl:ENSG00000213066 lincRNA,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1254907422 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5620641,Human_RBP_ID_15736027 RMVar_hsa_circ_36990,RMVar_hsa_circ_58227,RMVar_hsa_circ_31414,RMVar_hsa_circ_242987,RMVar_hsa_circ_283437,RMVar_hsa_circ_331352,RMVar_hsa_circ_242988,RMVar_hsa_circ_242986,RMVar_hsa_circ_110613,RMVar_hsa_circ_282372,RMVar_hsa_circ_360400,RMVar_hsa_circ_270934,RMVar_hsa_circ_242990,RMVar_hsa_circ_242992,RMVar_hsa_circ_242993,RMVar_hsa_circ_242991,RMVar_hsa_circ_62095,RMVar_hsa_circ_242996,RMVar_hsa_circ_242989,RMVar_hsa_circ_288093,RMVar_hsa_circ_318220,RMVar_hsa_circ_242997 37556 RMVar_ID_37556 Human_SNP_ID_306295025 A-to-I Human chr6 + 169703394 169703394 169703394 AAGGTTGATAACTTTGTAATTTTACTCTGGAGATTCTAACCGAAGTTGGTGTAAGTTTTCAAGAG AAGGTTGATAACTTTGTAATTTTACTCTGGAGGTTCTAACCGAAGTTGGTGTAAGTTTTCAAGAG A G C6orf120 Ensembl:ENSG00000185127 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968178073 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_657420,Human_RBP_ID_2014839,Human_RBP_ID_7575872,Human_RBP_ID_8898524,Human_RBP_ID_15742192,Human_RBP_ID_18368637,Human_RBP_ID_27752964 Human_miRNA_ID_613727,Human_miRNA_ID_617080,Human_miRNA_ID_1543811,Human_miRNA_ID_1596679 37557 RMVar_ID_37557 Human_SNP_ID_306296544 A-to-I Human chr6 - 169708690 169708690 169708690 TAATACAGGCTGGAAATCAGCTATTCAACACTATCATTGATTTAGTATACAAGAAATCATATGGA TAATACAGGCTGGAAATCAGCTATTCAACACTGTCATTGATTTAGTATACAAGAAATCATATGGA T C PHF10 Ensembl:ENSG00000130024 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs570849760 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_657527,Human_RBP_ID_8140666,Human_RBP_ID_8638238,Human_RBP_ID_17305668,Human_RBP_ID_17534851,Human_RBP_ID_18368716 RMVar_hsa_circ_61014,RMVar_hsa_circ_48343,RMVar_hsa_circ_60075 37558 RMVar_ID_37558 Human_SNP_ID_306299266 A-to-I Human chr6 - 169718920 169718920 169718920 ACATTTAATGCATAATATGTATTTCTGTACTTAGTTTTAGTTACTATCCAGCAGAAAACTTGATA ACATTTAATGCATAATATGTATTTCTGTACTTCGTTTTAGTTACTATCCAGCAGAAAACTTGATA T G PHF10 Ensembl:ENSG00000130024 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1337110731 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_80160,Human_RBP_ID_2995755,Human_RBP_ID_25986642 RMVar_hsa_circ_61014,RMVar_hsa_circ_60075,RMVar_hsa_circ_243121,RMVar_hsa_circ_279129,RMVar_hsa_circ_286365,RMVar_hsa_circ_27251,RMVar_hsa_circ_63430,RMVar_hsa_circ_243122,RMVar_hsa_circ_306928 37559 RMVar_ID_37559 Human_SNP_ID_306474931 A-to-I Human chr6 + 170359272 170359272 170359272 AAAATACAAAAATTAGCCAGGTGTGTGCCTGTAATCCTAGCTACTTGCAAGGCTGAGGCAATAGA AAAATACAAAAATTAGCCAGGTGTGTGCCTGTCATCCTAGCTACTTGCAAGGCTGAGGCAATAGA A C FAM120B Ensembl:ENSG00000112584 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs556759088 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17576572,Human_RBP_ID_18859198 RMVar_hsa_circ_114410,RMVar_hsa_circ_243140,RMVar_hsa_circ_378824 37560 RMVar_ID_37560 Human_SNP_ID_306483255 A-to-I Human chr6 + 170391373 170391373 170391373 CCTGGCCCACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATGAACCGGGCGTGTTGGCGG CCTGGCCCACATGGTGAAACCCCGTCTCTACTGAAAATACAAAAATGAACCGGGCGTGTTGGCGG A G FAM120B Ensembl:ENSG00000112584 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1204676408 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114410,RMVar_hsa_circ_243140,RMVar_hsa_circ_243154,RMVar_hsa_circ_332497,RMVar_hsa_circ_378824,RMVar_hsa_circ_301726,RMVar_hsa_circ_243153,RMVar_hsa_circ_45303 37561 RMVar_ID_37561 Human_SNP_ID_306483267 A-to-I Human chr6 + 170391414 170391400 170391415 AAAATGAACCGGGCGTGTTGGCGGGCGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGAAGGAGG AAAATGAACCGGGCGTGTT_______________TCCCAGCTACTTGGGAGGCTGAGGAAGGAGG TGGCGGGCGCCTGTAA T FAM120B Ensembl:ENSG00000112584 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1004905728 Functional Loss DEL dbSNP153 20..34 33 - - - RMVar_hsa_circ_114410,RMVar_hsa_circ_243140,RMVar_hsa_circ_243154,RMVar_hsa_circ_332497,RMVar_hsa_circ_378824,RMVar_hsa_circ_301726,RMVar_hsa_circ_243153,RMVar_hsa_circ_45303 37562 RMVar_ID_37562 Human_SNP_ID_306483274 A-to-I Human chr6 + 170391424 170391424 170391424 GGGCGTGTTGGCGGGCGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGAAGGAGGATCACTTGAA GGGCGTGTTGGCGGGCGCCTGTAATCCCAGCTGCTTGGGAGGCTGAGGAAGGAGGATCACTTGAA A G FAM120B Ensembl:ENSG00000112584 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs536615084 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114410,RMVar_hsa_circ_243140,RMVar_hsa_circ_243154,RMVar_hsa_circ_332497,RMVar_hsa_circ_378824,RMVar_hsa_circ_301726,RMVar_hsa_circ_243153,RMVar_hsa_circ_45303 37563 RMVar_ID_37563 Human_SNP_ID_306531363 A-to-I Human chr6 + 170567351 170567351 170567351 TACTAAAAATACAAAAATTAGCCAGGCGTGGTAGTGGATGTCTGTAGTCCCAGCTACTTGGGAGG TACTAAAAATACAAAAATTAGCCAGGCGTGGTGGTGGATGTCTGTAGTCCCAGCTACTTGGGAGG A G TBP Ensembl:ENSG00000112592 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1299478834 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19194,RMVar_hsa_circ_349069 37564 RMVar_ID_37564 Human_SNP_ID_650230083 A-to-I Human chr18 - 62174138 62174138 62174138 ATGATCTTGGTTCACTGTAAACTCCGCCTCCCAGATTCAAGTGATTTTCCTGCCTCAGCCTCCTG ATGATCTTGGTTCACTGTAAACTCCGCCTCCCTGATTCAAGTGATTTTCCTGCCTCAGCCTCCTG T A PIGN Ensembl:ENSG00000197563 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1327189076 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107926,RMVar_hsa_circ_190504,RMVar_hsa_circ_343686 37565 RMVar_ID_37565 Human_SNP_ID_650244980 A-to-I Human chr18 + 62240855 62240855 62240855 TTAGCTGGGCACAGTGGCACATAGTTCCTGCTACTAAGGAGGCTGAGGCAGGAGGATCTTGTGGA TTAGCTGGGCACAGTGGCACATAGTTCCTGCTCCTAAGGAGGCTGAGGCAGGAGGATCTTGTGGA A C RELCH Ensembl:ENSG00000134444 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1313889898 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23319,RMVar_hsa_circ_103348,RMVar_hsa_circ_333851,RMVar_hsa_circ_304418,RMVar_hsa_circ_354987,RMVar_hsa_circ_32503,RMVar_hsa_circ_190510,RMVar_hsa_circ_43419,RMVar_hsa_circ_190511,RMVar_hsa_circ_55694,RMVar_hsa_circ_100671,RMVar_hsa_circ_71852,RMVar_hsa_circ_328293,RMVar_hsa_circ_190515 37566 RMVar_ID_37566 Human_SNP_ID_650244982 A-to-I Human chr18 + 62240858 62240858 62240858 GCTGGGCACAGTGGCACATAGTTCCTGCTACTAAGGAGGCTGAGGCAGGAGGATCTTGTGGAGTT GCTGGGCACAGTGGCACATAGTTCCTGCTACTCAGGAGGCTGAGGCAGGAGGATCTTGTGGAGTT A C RELCH Ensembl:ENSG00000134444 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs943500023 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6699374,Human_RBP_ID_13328480 RMVar_hsa_circ_23319,RMVar_hsa_circ_103348,RMVar_hsa_circ_333851,RMVar_hsa_circ_304418,RMVar_hsa_circ_354987,RMVar_hsa_circ_32503,RMVar_hsa_circ_190510,RMVar_hsa_circ_43419,RMVar_hsa_circ_190511,RMVar_hsa_circ_55694,RMVar_hsa_circ_100671,RMVar_hsa_circ_71852,RMVar_hsa_circ_328293,RMVar_hsa_circ_190515 37567 RMVar_ID_37567 Human_SNP_ID_650306157 A-to-I Human chr18 - 62508672 62508672 62508672 CCTTGGCCTCCCAAAGTGCTGGGCTTACAGGTATGAGCCATCACTCCTGGCCTAGGACTGAGTTA CCTTGGCCTCCCAAAGTGCTGGGCTTACAGGTGTGAGCCATCACTCCTGGCCTAGGACTGAGTTA T C lnc-PIGN-7 RNACentral:URS0000D58386 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs368618234 Functional Loss SNV dbSNP153 33..33 33 - - - 37568 RMVar_ID_37568 Human_SNP_ID_650495970 A-to-I Human chr18 - 63275229 63275228 63275229 AAAATTATTTCCCTTTTTTTTTTTTTTGAGACAGGGTCTGACTCTGTCACCCAGGCTGGAGTGGT AAAATTATTTCCCTTTTTTTTTTTTTTGAGAC_GGGTCTGACTCTGTCACCCAGGCTGGAGTGGT CT C BCL2 Ensembl:ENSG00000171791 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1171637876 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_13330153 37569 RMVar_ID_37569 Human_SNP_ID_650495974 A-to-I Human chr18 - 63275233 63275233 63275233 ATCGAAAATTATTTCCCTTTTTTTTTTTTTTGAGACAGGGTCTGACTCTGTCACCCAGGCTGGAG ATCGAAAATTATTTCCCTTTTTTTTTTTTTTGTGACAGGGTCTGACTCTGTCACCCAGGCTGGAG T A BCL2 Ensembl:ENSG00000171791 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232398719 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13330153 37570 RMVar_ID_37570 Human_SNP_ID_650500949 A-to-I Human chr18 - 63296333 63296333 63296333 TGATTGTGCCACTCCACTCCAGCCTGGATGACAGAGTGAGACCTTGTCTCAAAAAAAAGGACTTC TGATTGTGCCACTCCACTCCAGCCTGGATGACGGAGTGAGACCTTGTCTCAAAAAAAAGGACTTC T C BCL2 Ensembl:ENSG00000171791 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs959108784 Functional Loss SNV dbSNP153 33..33 33 - - - 37571 RMVar_ID_37571 Human_SNP_ID_650500955 A-to-I Human chr18 - 63296355 63296355 63296355 AGGTTGAGGCTGCAGTGAGCCATGATTGTGCCACTCCACTCCAGCCTGGATGACAGAGTGAGACC AGGTTGAGGCTGCAGTGAGCCATGATTGTGCCGCTCCACTCCAGCCTGGATGACAGAGTGAGACC T C BCL2 Ensembl:ENSG00000171791 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1336312543 Functional Loss SNV dbSNP153 33..33 33 - - - 37572 RMVar_ID_37572 Human_SNP_ID_650500959 A-to-I Human chr18 - 63296366 63296366 63296366 GCTGAGATGGGAGGTTGAGGCTGCAGTGAGCCATGATTGTGCCACTCCACTCCAGCCTGGATGAC GCTGAGATGGGAGGTTGAGGCTGCAGTGAGCCGTGATTGTGCCACTCCACTCCAGCCTGGATGAC T C BCL2 Ensembl:ENSG00000171791 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1309597604 Functional Loss SNV dbSNP153 33..33 33 - - - 37573 RMVar_ID_37573 Human_SNP_ID_650501755 A-to-I Human chr18 - 63299838 63299838 63299838 GGTGCCGTTTGGCCTGGGCTTGAAGGATACATAAGAGTTTGTTCAAAAAAAAAAAGAAAAAGAAA GGTGCCGTTTGGCCTGGGCTTGAAGGATACATGAGAGTTTGTTCAAAAAAAAAAAGAAAAAGAAA T C BCL2 Ensembl:ENSG00000171791 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404117555 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25371320 37574 RMVar_ID_37574 Human_SNP_ID_650501756 A-to-I Human chr18 - 63299840 63299839 63299840 AAGGTGCCGTTTGGCCTGGGCTTGAAGGATACATAAGAGTTTGTTCAAAAAAAAAAAGAAAAAGA AAGGTGCCGTTTGGCCTGGGCTTGAAGGATAC_TAAGAGTTTGTTCAAAAAAAAAAAGAAAAAGA AT A BCL2 Ensembl:ENSG00000171791 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432030401 Functional Loss DEL dbSNP153 33..33 33 - - - 37575 RMVar_ID_37575 Human_SNP_ID_650501757 A-to-I Human chr18 - 63299840 63299840 63299840 AAGGTGCCGTTTGGCCTGGGCTTGAAGGATACATAAGAGTTTGTTCAAAAAAAAAAAGAAAAAGA AAGGTGCCGTTTGGCCTGGGCTTGAAGGATACGTAAGAGTTTGTTCAAAAAAAAAAAGAAAAAGA T C BCL2 Ensembl:ENSG00000171791 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1011306173 Functional Loss SNV dbSNP153 33..33 33 - - - 37576 RMVar_ID_37576 Human_SNP_ID_650510929 A-to-I Human chr18 - 63337761 63337761 63337761 ACCACACCTGGCTAATTTTTTGTATTTGTAGTAGAAATGGGGCTTCACCATGTTGGCCAGGCTGG ACCACACCTGGCTAATTTTTTGTATTTGTAGTTGAAATGGGGCTTCACCATGTTGGCCAGGCTGG T A KDSR Ensembl:ENSG00000119537 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs955845084 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91806,RMVar_hsa_circ_23638,RMVar_hsa_circ_190562,RMVar_hsa_circ_269650,RMVar_hsa_circ_331036 37577 RMVar_ID_37577 Human_SNP_ID_650524870 A-to-I Human chr18 - 63394607 63394607 63394607 CAAAAATTAGCTCGGCGTCAGGGCGGGCGCCTATAATCCCAGCTACTCGGGAGGCTGAGGCAGGA CAAAAATTAGCTCGGCGTCAGGGCGGGCGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGA T C VPS4B Ensembl:ENSG00000119541 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs750975952 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5859 37578 RMVar_ID_37578 Human_SNP_ID_650532477 A-to-I Human chr18 + 63424852 63424852 63424852 TGCTCCTCAAAAATGTCAAGATCATAAAAGACAAGGAAAGACTGAGGAACTGTCACAGATTGTAG TGCTCCTCAAAAATGTCAAGATCATAAAAGACGAGGAAAGACTGAGGAACTGTCACAGATTGTAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1378843193 Functional Loss SNV dbSNP153 33..33 33 - - - 37579 RMVar_ID_37579 Human_SNP_ID_650547318 A-to-I Human chr18 - 63483112 63483112 63483112 CACATCTCAGAGCTCTTTAATTTTAACACAGCAACTTCCAAAGTGTTGTGTCTTGACTCCTGGCA CACATCTCAGAGCTCTTTAATTTTAACACAGCTACTTCCAAAGTGTTGTGTCTTGACTCCTGGCA T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1263198994 Functional Loss SNV dbSNP153 33..33 33 - - - 37580 RMVar_ID_37580 Human_SNP_ID_651331807 A-to-I Human chr18 - 66505086 66505086 66505086 GAAAACCACAAGCGCTGAGATCAGGAGCCTATACAGGCAGTCTTTGCAAGTTGGCCCCGACAGTG GAAAACCACAAGCGCTGAGATCAGGAGCCTATGCAGGCAGTCTTTGCAAGTTGGCCCCGACAGTG T C CDH19 Ensembl:ENSG00000071991 Protein coding CDS GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs751703202 Functional Loss SNV dbSNP153 33..33 33 - - - 37581 RMVar_ID_37581 Human_SNP_ID_651579007 A-to-I Human chr18 - 67507175 67507175 67507175 GCTTGGCTCATTTTTGTATTTTTAGTAGTGACAGCGTTTCACCACATTGGTCAGGCTGGTCTCAA GCTTGGCTCATTTTTGTATTTTTAGTAGTGACGGCGTTTCACCACATTGGTCAGGCTGGTCTCAA T C DSEL Ensembl:ENSG00000171451 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1440798204 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13330835 37582 RMVar_ID_37582 Human_SNP_ID_651579024 A-to-I Human chr18 - 67507260 67507260 67507260 TCACTGCAACCTCCGCCTACCGGGTTCAAGTGATTCTCCTACGTCAGCCTCCTGAATAGCTGGGA TCACTGCAACCTCCGCCTACCGGGTTCAAGTGTTTCTCCTACGTCAGCCTCCTGAATAGCTGGGA T A DSEL Ensembl:ENSG00000171451 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941116910 Functional Loss SNV dbSNP153 33..33 33 - - - 37583 RMVar_ID_37583 Human_SNP_ID_651579042 A-to-I Human chr18 - 67507333 67507333 67507333 TTTTTTTTTTTTTTTTTTTGGGATGGAGTCTCACTTTGTTGCCCAGGCTGGAGTGCAGTGGTCTG TTTTTTTTTTTTTTTTTTTGGGATGGAGTCTCGCTTTGTTGCCCAGGCTGGAGTGCAGTGGTCTG T C DSEL Ensembl:ENSG00000171451 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1487873546 Functional Loss SNV dbSNP153 33..33 33 - - - 37584 RMVar_ID_37584 Human_SNP_ID_652154396 A-to-I Human chr18 + 69777993 69777993 69777993 GGAAGGATATAAAGCAGACTAAAGTGCTCATCAAAGTAAATTGAAAATAATGATAAATGCTTCAC GGAAGGATATAAAGCAGACTAAAGTGCTCATCGAAGTAAATTGAAAATAATGATAAATGCTTCAC A G DOK6 Ensembl:ENSG00000206052 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs3786256 Functional Loss SNV dbSNP153,JSNP 33..33 33 - - - GWAS_ID_4320,GWAS_ID_4321 37585 RMVar_ID_37585 Human_SNP_ID_652173123 A-to-I Human chr18 - 69858868 69858868 69858868 AAAATTAGCCAGGCCTGGTGGCACGCACCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGAAGA AAAATTAGCCAGGCCTGGTGGCACGCACCTGTGGTCCCAGCTACTTGGGAGGCTGAGGCAGAAGA T C CD226 Ensembl:ENSG00000150637 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1188740205 Functional Loss SNV dbSNP153 33..33 33 - - - 37586 RMVar_ID_37586 Human_SNP_ID_652204954 A-to-I Human chr18 - 69985080 69985080 69985080 CCTATAATCCCAGCTACTCGGGAGGCTGAGGCAGTAGAATTGCTTGAACCCAGAGGCGGGGGTTG CCTATAATCCCAGCTACTCGGGAGGCTGAGGCGGTAGAATTGCTTGAACCCAGAGGCGGGGGTTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1319061532 Functional Loss SNV dbSNP153 33..33 33 - - - 37587 RMVar_ID_37587 Human_SNP_ID_652285553 A-to-I Human chr18 + 70317868 70317868 70317868 CACCAACATCGTTTTGTTTGTTTGTTTGAGACAGGGCCCTACACTCGGTCACCCAGGTTGGTGTG CACCAACATCGTTTTGTTTGTTTGTTTGAGACCGGGCCCTACACTCGGTCACCCAGGTTGGTGTG A C SOCS6 Ensembl:ENSG00000170677 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1446710022 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13333508 37588 RMVar_ID_37588 Human_SNP_ID_652914533 A-to-I Human chr18 - 72765681 72765681 72765681 CTGGCACTGTGGCTCACGCCTGTAACCTCAGCACTTTGGGAGGCCAAGGTGGGTGGATCATGAGG CTGGCACTGTGGCTCACGCCTGTAACCTCAGCCCTTTGGGAGGCCAAGGTGGGTGGATCATGAGG T G NETO1 Ensembl:ENSG00000166342 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1160655511 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40586,RMVar_hsa_circ_267705 37589 RMVar_ID_37589 Human_SNP_ID_652914601 A-to-I Human chr18 - 72766024 72766024 72766024 TTTTGTATTTTTAGTAGAGATGAGTTCTCACCATGTTGACCGAGCTGGTCTTGAACTCCTGACCT TTTTGTATTTTTAGTAGAGATGAGTTCTCACCTTGTTGACCGAGCTGGTCTTGAACTCCTGACCT T A NETO1 Ensembl:ENSG00000166342 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs982424699 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40586,RMVar_hsa_circ_267705 37590 RMVar_ID_37590 Human_SNP_ID_652914602 A-to-I Human chr18 - 72766024 72766024 72766024 TTTTGTATTTTTAGTAGAGATGAGTTCTCACCATGTTGACCGAGCTGGTCTTGAACTCCTGACCT TTTTGTATTTTTAGTAGAGATGAGTTCTCACCGTGTTGACCGAGCTGGTCTTGAACTCCTGACCT T C NETO1 Ensembl:ENSG00000166342 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs982424699 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40586,RMVar_hsa_circ_267705 37591 RMVar_ID_37591 Human_SNP_ID_652937321 A-to-I Human chr18 - 72853514 72853514 72853514 GCCTCAAGTGATCCGCCCACCTCAGCCCCCCAAATGCTAGGATCACAGGCGTGAGCCACCACATC GCCTCAAGTGATCCGCCCACCTCAGCCCCCCAGATGCTAGGATCACAGGCGTGAGCCACCACATC T C NETO1 Ensembl:ENSG00000166342 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1374964052 Functional Loss SNV dbSNP153 33..33 33 - - - 37592 RMVar_ID_37592 Human_SNP_ID_653271804 A-to-I Human chr18 + 74158484 74158484 74158484 TTGAAGATAATCGATCCCAAGATGATTAAAATAGGGTTTCTGATGGATGTTGAATGGCGTGGACT TTGAAGATAATCGATCCCAAGATGATTAAAATCGGGTTTCTGATGGATGTTGAATGGCGTGGACT A C TIMM21 Ensembl:ENSG00000075336 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs8148 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3559380,Human_RBP_ID_23776855 37593 RMVar_ID_37593 Human_SNP_ID_653271805 A-to-I Human chr18 + 74158484 74158484 74158484 TTGAAGATAATCGATCCCAAGATGATTAAAATAGGGTTTCTGATGGATGTTGAATGGCGTGGACT TTGAAGATAATCGATCCCAAGATGATTAAAATGGGGTTTCTGATGGATGTTGAATGGCGTGGACT A G TIMM21 Ensembl:ENSG00000075336 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs8148 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3559380,Human_RBP_ID_23776855 37594 RMVar_ID_37594 Human_SNP_ID_653271806 A-to-I Human chr18 + 74158484 74158484 74158484 TTGAAGATAATCGATCCCAAGATGATTAAAATAGGGTTTCTGATGGATGTTGAATGGCGTGGACT TTGAAGATAATCGATCCCAAGATGATTAAAATTGGGTTTCTGATGGATGTTGAATGGCGTGGACT A T TIMM21 Ensembl:ENSG00000075336 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs8148 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3559380,Human_RBP_ID_23776855 37595 RMVar_ID_37595 Human_SNP_ID_653329970 A-to-I Human chr18 + 74390250 74390250 74390250 TGAGCCTTGATCTGGGCGACCATTTCCTGGCCAGTCACCTCAAGGGTGTGTAGCTCCTGGGCGCG TGAGCCTTGATCTGGGCGACCATTTCCTGGCCGGTCACCTCAAGGGTGTGTAGCTCCTGGGCGCG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878877212 Functional Loss SNV dbSNP153 33..33 33 - - - 37596 RMVar_ID_37596 Human_SNP_ID_653388687 A-to-I Human chr18 + 74615928 74615922 74615928 TCTTTTTGTCCGGGCTGGAGTGCAATGGCATGATCTCGGCTCACTGCAGCTTCCGCCTCCCGGGT TCTTTTTGTCCGGGCTGGAGTGCAATG______TCTCGGCTCACTGCAGCTTCCGCCTCCCGGGT GGCATGA G ZNF407 Ensembl:ENSG00000215421 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1212800563 Functional Loss DEL dbSNP153 28..33 33 - - - 37597 RMVar_ID_37597 Human_SNP_ID_587181883 A-to-I Human chr15 + 90002938 90002938 90002938 CTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCGATCTCGGCTCACTGCAGCCTCCGTCTCCCGGGT CTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCGTTCTCGGCTCACTGCAGCCTCCGTCTCCCGGGT A T ZNF710 Ensembl:ENSG00000140548 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335863188 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111859,RMVar_hsa_circ_174715,RMVar_hsa_circ_95129,RMVar_hsa_circ_174714 37598 RMVar_ID_37598 Human_SNP_ID_587189551 A-to-I Human chr15 + 90032200 90032200 90032200 TTGTATTTTTAGTAGAGACAGAGTTTTGCCATATTGGCCAGGCTGGTCTCGAGCTCCCAACCTCA TTGTATTTTTAGTAGAGACAGAGTTTTGCCATGTTGGCCAGGCTGGTCTCGAGCTCCCAACCTCA A G ZNF710 Ensembl:ENSG00000140548 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs951822792 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111859,RMVar_hsa_circ_174715,RMVar_hsa_circ_95129,RMVar_hsa_circ_174714 37599 RMVar_ID_37599 Human_SNP_ID_587200977 A-to-I Human chr15 - 90075321 90075321 90075321 AGACCAGGTCTCACTATGTTGCCTGGTTTGGTATCAAACTCCTGGCCTTAAGGGATCCTCCTGCC AGACCAGGTCTCACTATGTTGCCTGGTTTGGTGTCAAACTCCTGGCCTTAAGGGATCCTCCTGCC T C ZNF710-AS1 Ensembl:ENSG00000259291 lincRNA exon GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs922027931 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26437876 37600 RMVar_ID_37600 Human_SNP_ID_587201634 A-to-I Human chr15 - 90077883 90077883 90077883 TCTTTTTTTGACAAGGTCTTGCTCTATTGCCAAGGCTGGGGTGCAGTGGTGCAATCATGGCTCAC TCTTTTTTTGACAAGGTCTTGCTCTATTGCCAGGGCTGGGGTGCAGTGGTGCAATCATGGCTCAC T C ZNF710-AS1 Ensembl:ENSG00000259291 lincRNA intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1366873194 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26437880 37601 RMVar_ID_37601 Human_SNP_ID_587201635 A-to-I Human chr15 - 90077883 90077883 90077883 TCTTTTTTTGACAAGGTCTTGCTCTATTGCCAAGGCTGGGGTGCAGTGGTGCAATCATGGCTCAC TCTTTTTTTGACAAGGTCTTGCTCTATTGCCACGGCTGGGGTGCAGTGGTGCAATCATGGCTCAC T G ZNF710-AS1 Ensembl:ENSG00000259291 lincRNA intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1366873194 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26437880 37602 RMVar_ID_37602 Human_SNP_ID_587203015 A-to-I Human chr15 - 90082926 90082926 90082926 AGTCCTGGCCAGGTGTGGTGGCTCATGCCTATAGTCCCAGCACTTTGGGAGGCCAAGGTGGGAGG AGTCCTGGCCAGGTGTGGTGGCTCATGCCTATGGTCCCAGCACTTTGGGAGGCCAAGGTGGGAGG T C - - Other Unknown GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1330022743 Functional Loss SNV dbSNP153 33..33 33 - - - 37603 RMVar_ID_37603 Human_SNP_ID_587203016 A-to-I Human chr15 - 90082928 90082928 90082928 AAAGTCCTGGCCAGGTGTGGTGGCTCATGCCTATAGTCCCAGCACTTTGGGAGGCCAAGGTGGGA AAAGTCCTGGCCAGGTGTGGTGGCTCATGCCTGTAGTCCCAGCACTTTGGGAGGCCAAGGTGGGA T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs908366178 Functional Loss SNV dbSNP153 33..33 33 - - - 37604 RMVar_ID_37604 Human_SNP_ID_587206387 A-to-I Human chr15 - 90093815 90093815 90093815 AGGAGTTCGAGACCAGCCTGGCCAACATGGCAAAACCCCGTCTCTACTAAAAATACAAAAATTAG AGGAGTTCGAGACCAGCCTGGCCAACATGGCAGAACCCCGTCTCTACTAAAAATACAAAAATTAG T C IDH2 Ensembl:ENSG00000182054 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs752695402 Functional Loss SNV dbSNP153 33..33 33 - - - 37605 RMVar_ID_37605 Human_SNP_ID_587233077 A-to-I Human chr15 + 90188700 90188699 90188701 CGTATTGTCTTTTTTTGTTTGTTTTTTGAGACAGAGTCTCGCTCACTCTGGGTGCAGTGGCGCTA CGTATTGTCTTTTTTTGTTTGTTTTTTGAGAC__AGTCTCGCTCACTCTGGGTGCAGTGGCGCTA CAG C SEMA4B Ensembl:ENSG00000185033 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs200111840 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_90524,RMVar_hsa_circ_174728 37606 RMVar_ID_37606 Human_SNP_ID_587233198 A-to-I Human chr15 + 90188930 90188930 90188930 TGACCTCGTGATCCGCCCGCCTCAGCCTCCCAAAGTGCTGGGATTATAGGCATGAGCCACCGCGC TGACCTCGTGATCCGCCCGCCTCAGCCTCCCACAGTGCTGGGATTATAGGCATGAGCCACCGCGC A C SEMA4B Ensembl:ENSG00000185033 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1453509095 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90524,RMVar_hsa_circ_174728 37607 RMVar_ID_37607 Human_SNP_ID_587257972 A-to-I Human chr15 + 90272596 90272596 90272596 TACTTGGGAGGCCGAGGTGGGAGAATCGCTTGAGCCTCGGAGGTTGAGGCTGCAGTGAGCTATGA TACTTGGGAGGCCGAGGTGGGAGAATCGCTTGGGCCTCGGAGGTTGAGGCTGCAGTGAGCTATGA A G NGRN,AC091167.6 Ensembl:ENSG00000182768,Ensembl:ENSG00000275674 Protein coding,Protein coding exon,intron GSE38233;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;Bronchiolar epithelium,BERP35T4 cell line - 24183664,31158229 RNA-Seq:(High) rs541419887 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22195632,Human_RBP_ID_25178215 37608 RMVar_ID_37608 Human_SNP_ID_587258299 A-to-I Human chr15 + 90273898 90273898 90273898 TGGCCTTTATTTTTCTTTTGAGACAGGGTCTCACTCTTGTCGTCCACACTGGAGTACAGTGGCTC TGGCCTTTATTTTTCTTTTGAGACAGGGTCTCTCTCTTGTCGTCCACACTGGAGTACAGTGGCTC A T NGRN,AC091167.6 Ensembl:ENSG00000182768,Ensembl:ENSG00000275674 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1000053170 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8425781 37609 RMVar_ID_37609 Human_SNP_ID_587259215 A-to-I Human chr15 + 90276796 90276796 90276796 TATTTTTAGTAGAGACAGGGTTTTACCGTGTTAGCCATGATGGTCTCGATCTCCTGACCTCGTGA TATTTTTAGTAGAGACAGGGTTTTACCGTGTTGGCCATGATGGTCTCGATCTCCTGACCTCGTGA A G AC091167.6 Ensembl:ENSG00000275674 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1249025759 Functional Loss SNV dbSNP153 33..33 33 - - - 37610 RMVar_ID_37610 Human_SNP_ID_587259387 A-to-I Human chr15 + 90277654 90277654 90277654 AGAATTAGCCAGGTATGGTTGCACAGGCCTGTAATCCCAGCTACCCGGGAGGCTGAGGCAGGAGA AGAATTAGCCAGGTATGGTTGCACAGGCCTGTGATCCCAGCTACCCGGGAGGCTGAGGCAGGAGA A G AC091167.6 Ensembl:ENSG00000275674 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1132416 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_466929 37611 RMVar_ID_37611 Human_SNP_ID_587259393 A-to-I Human chr15 + 90277681 90277681 90277681 CCTGTAATCCCAGCTACCCGGGAGGCTGAGGCAGGAGAATCACCTGAACCTGAGAGGCAGAGGCT CCTGTAATCCCAGCTACCCGGGAGGCTGAGGCGGGAGAATCACCTGAACCTGAGAGGCAGAGGCT A G AC091167.6 Ensembl:ENSG00000275674 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1132420 Functional Loss SNV dbSNP153 33..33 33 - - - 37612 RMVar_ID_37612 Human_SNP_ID_587259400 A-to-I Human chr15 + 90277701 90277701 90277701 GGAGGCTGAGGCAGGAGAATCACCTGAACCTGAGAGGCAGAGGCTTCAGTGAGCCGAGGCCACAC GGAGGCTGAGGCAGGAGAATCACCTGAACCTGGGAGGCAGAGGCTTCAGTGAGCCGAGGCCACAC A G AC091167.6 Ensembl:ENSG00000275674 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1158000518 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17869147 37613 RMVar_ID_37613 Human_SNP_ID_587259402 A-to-I Human chr15 + 90277707 90277707 90277707 TGAGGCAGGAGAATCACCTGAACCTGAGAGGCAGAGGCTTCAGTGAGCCGAGGCCACACCACTGC TGAGGCAGGAGAATCACCTGAACCTGAGAGGCGGAGGCTTCAGTGAGCCGAGGCCACACCACTGC A G AC091167.6 Ensembl:ENSG00000275674 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1567085098 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17869147 37614 RMVar_ID_37614 Human_SNP_ID_587260079 A-to-I Human chr15 + 90279891 90279891 90279891 ACAGAGTCTAACTCTGTTGCCTAGGCTGGAGTACAACGGCACGGTCCTGGCTCACTGAAACCTCC ACAGAGTCTAACTCTGTTGCCTAGGCTGGAGTGCAACGGCACGGTCCTGGCTCACTGAAACCTCC A G AC091167.6 Ensembl:ENSG00000275674 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1485190118 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6479176 37615 RMVar_ID_37615 Human_SNP_ID_587261657 A-to-I Human chr15 + 90286375 90286375 90286375 TGTACAAAAAATATAATAAATTGGCAGGGCACAGTGGTGCCTGTGGATGCAGCTGCTGGGGAGGC TGTACAAAAAATATAATAAATTGGCAGGGCACGGTGGTGCCTGTGGATGCAGCTGCTGGGGAGGC A G AC091167.6 Ensembl:ENSG00000275674 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1471143368 Functional Loss SNV dbSNP153 33..33 33 - - - 37616 RMVar_ID_37616 Human_SNP_ID_587285405 A-to-I Human chr15 + 90376390 90376390 90376390 ATGATCTGCCCGCCTCAGCCTCCCAAAGTGTTAGGATTACAGGCCTGAGCCACCGCACCCGACCC ATGATCTGCCCGCCTCAGCCTCCCAAAGTGTTGGGATTACAGGCCTGAGCCACCGCACCCGACCC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs527866288 Functional Loss SNV dbSNP153 33..33 33 - - - 37617 RMVar_ID_37617 Human_SNP_ID_587289053 A-to-I Human chr15 + 90389870 90389870 90389870 TCCCAGCTGCTTGGGGCTGAGGTAGGAGGATCATTTGAGCCCAGAAAGTCGAGGCTGCAGTAAGC TCCCAGCTGCTTGGGGCTGAGGTAGGAGGATCCTTTGAGCCCAGAAAGTCGAGGCTGCAGTAAGC A C IQGAP1 Ensembl:ENSG00000140575 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1040936706 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79616,RMVar_hsa_circ_124073,RMVar_hsa_circ_174760,RMVar_hsa_circ_174761 37618 RMVar_ID_37618 Human_SNP_ID_587289054 A-to-I Human chr15 + 90389870 90389870 90389870 TCCCAGCTGCTTGGGGCTGAGGTAGGAGGATCATTTGAGCCCAGAAAGTCGAGGCTGCAGTAAGC TCCCAGCTGCTTGGGGCTGAGGTAGGAGGATCTTTTGAGCCCAGAAAGTCGAGGCTGCAGTAAGC A T IQGAP1 Ensembl:ENSG00000140575 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1040936706 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79616,RMVar_hsa_circ_124073,RMVar_hsa_circ_174760,RMVar_hsa_circ_174761 37619 RMVar_ID_37619 Human_SNP_ID_587299197 A-to-I Human chr15 + 90427187 90427187 90427187 GGGAGACTGAGGCAAGAGGATTGCTTGAGCCTAGGAGGTTGAGGCTGTAGGGAGTTAGTATTGCG GGGAGACTGAGGCAAGAGGATTGCTTGAGCCTGGGAGGTTGAGGCTGTAGGGAGTTAGTATTGCG A G IQGAP1 Ensembl:ENSG00000140575 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1029731235 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43673,RMVar_hsa_circ_80929,RMVar_hsa_circ_79616,RMVar_hsa_circ_124073,RMVar_hsa_circ_174760,RMVar_hsa_circ_174761,RMVar_hsa_circ_117467,RMVar_hsa_circ_76067,RMVar_hsa_circ_112963,RMVar_hsa_circ_174762,RMVar_hsa_circ_174763,RMVar_hsa_circ_295457,RMVar_hsa_circ_92142,RMVar_hsa_circ_55945,RMVar_hsa_circ_174765,RMVar_hsa_circ_174766,RMVar_hsa_circ_174767,RMVar_hsa_circ_174764 37620 RMVar_ID_37620 Human_SNP_ID_587300884 A-to-I Human chr15 + 90434181 90434181 90434181 TTTATAAGCCGGATGCGGTGGCTCACGCCTGTAATCCCAGCATTTTGGGAGGCCAAGGCGGGTGG TTTATAAGCCGGATGCGGTGGCTCACGCCTGTCATCCCAGCATTTTGGGAGGCCAAGGCGGGTGG A C IQGAP1 Ensembl:ENSG00000140575 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs963287916 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80929,RMVar_hsa_circ_79616,RMVar_hsa_circ_124073,RMVar_hsa_circ_174760,RMVar_hsa_circ_174761,RMVar_hsa_circ_117467,RMVar_hsa_circ_76067,RMVar_hsa_circ_112963,RMVar_hsa_circ_174762,RMVar_hsa_circ_174763,RMVar_hsa_circ_92142,RMVar_hsa_circ_55945,RMVar_hsa_circ_93137,RMVar_hsa_circ_113637,RMVar_hsa_circ_174765,RMVar_hsa_circ_174766,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_174770,RMVar_hsa_circ_174771 37621 RMVar_ID_37621 Human_SNP_ID_587301724 A-to-I Human chr15 + 90437643 90437643 90437643 GACTCATTGTAACAACCTCCCAGGCACAAGCTATCCTCCTGCCTTAGCCTCCCAAATGGCTAGGA GACTCATTGTAACAACCTCCCAGGCACAAGCTGTCCTCCTGCCTTAGCCTCCCAAATGGCTAGGA A G IQGAP1 Ensembl:ENSG00000140575 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs964755473 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80929,RMVar_hsa_circ_79616,RMVar_hsa_circ_124073,RMVar_hsa_circ_174760,RMVar_hsa_circ_174761,RMVar_hsa_circ_117467,RMVar_hsa_circ_76067,RMVar_hsa_circ_112963,RMVar_hsa_circ_174762,RMVar_hsa_circ_174763,RMVar_hsa_circ_92142,RMVar_hsa_circ_55945,RMVar_hsa_circ_93137,RMVar_hsa_circ_113637,RMVar_hsa_circ_174765,RMVar_hsa_circ_174766,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_174770,RMVar_hsa_circ_174771 37622 RMVar_ID_37622 Human_SNP_ID_587301725 A-to-I Human chr15 + 90437643 90437643 90437643 GACTCATTGTAACAACCTCCCAGGCACAAGCTATCCTCCTGCCTTAGCCTCCCAAATGGCTAGGA GACTCATTGTAACAACCTCCCAGGCACAAGCTTTCCTCCTGCCTTAGCCTCCCAAATGGCTAGGA A T IQGAP1 Ensembl:ENSG00000140575 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs964755473 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80929,RMVar_hsa_circ_79616,RMVar_hsa_circ_124073,RMVar_hsa_circ_174760,RMVar_hsa_circ_174761,RMVar_hsa_circ_117467,RMVar_hsa_circ_76067,RMVar_hsa_circ_112963,RMVar_hsa_circ_174762,RMVar_hsa_circ_174763,RMVar_hsa_circ_92142,RMVar_hsa_circ_55945,RMVar_hsa_circ_93137,RMVar_hsa_circ_113637,RMVar_hsa_circ_174765,RMVar_hsa_circ_174766,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_174770,RMVar_hsa_circ_174771 37623 RMVar_ID_37623 Human_SNP_ID_587301742 A-to-I Human chr15 + 90437740 90437740 90437740 AAGAAATTTTTTTTGTAGAGACAAGTCTTGCTATGTTGCTCAAGCTGTTTTGAATTCCTGACCTC AAGAAATTTTTTTTGTAGAGACAAGTCTTGCTGTGTTGCTCAAGCTGTTTTGAATTCCTGACCTC A G IQGAP1 Ensembl:ENSG00000140575 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1461840612 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2459446 RMVar_hsa_circ_80929,RMVar_hsa_circ_79616,RMVar_hsa_circ_124073,RMVar_hsa_circ_174760,RMVar_hsa_circ_174761,RMVar_hsa_circ_117467,RMVar_hsa_circ_76067,RMVar_hsa_circ_112963,RMVar_hsa_circ_174762,RMVar_hsa_circ_174763,RMVar_hsa_circ_92142,RMVar_hsa_circ_55945,RMVar_hsa_circ_93137,RMVar_hsa_circ_113637,RMVar_hsa_circ_174765,RMVar_hsa_circ_174766,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_174770,RMVar_hsa_circ_174771 37624 RMVar_ID_37624 Human_SNP_ID_587303151 A-to-I Human chr15 + 90443029 90443029 90443029 TCACCTAGGCTGGAGTGCAGTGGCACGGTCATAACTCACTGCAGCCTTGAACTTCTGGGGAAAGC TCACCTAGGCTGGAGTGCAGTGGCACGGTCATTACTCACTGCAGCCTTGAACTTCTGGGGAAAGC A T IQGAP1 Ensembl:ENSG00000140575 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs764079300 Functional Loss SNV dbSNP153 33..33 33 - - - 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_283346,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_335414,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_174777,RMVar_hsa_circ_174776,RMVar_hsa_circ_174773,RMVar_hsa_circ_174774,RMVar_hsa_circ_174772,RMVar_hsa_circ_52417,RMVar_hsa_circ_105113,RMVar_hsa_circ_174781,RMVar_hsa_circ_80566,RMVar_hsa_circ_110777,RMVar_hsa_circ_289597,RMVar_hsa_circ_309798,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_174783,RMVar_hsa_circ_174785,RMVar_hsa_circ_174786,RMVar_hsa_circ_174784,RMVar_hsa_circ_174782 37625 RMVar_ID_37625 Human_SNP_ID_587312013 A-to-I Human chr15 + 90475251 90475251 90475251 GAAGTCCTGACCTCGGGTGATCCACCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG GAAGTCCTGACCTCGGGTGATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG A G IQGAP1 Ensembl:ENSG00000140575 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1016168508 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124073,RMVar_hsa_circ_174761,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_96141,RMVar_hsa_circ_127514,RMVar_hsa_circ_174773,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_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_90067,RMVar_hsa_circ_27438,RMVar_hsa_circ_88952,RMVar_hsa_circ_174808,RMVar_hsa_circ_85108,RMVar_hsa_circ_106849,RMVar_hsa_circ_174811,RMVar_hsa_circ_174812,RMVar_hsa_circ_114375,RMVar_hsa_circ_174813,RMVar_hsa_circ_64383,RMVar_hsa_circ_84291,RMVar_hsa_circ_174814,RMVar_hsa_circ_174815,RMVar_hsa_circ_174816 37626 RMVar_ID_37626 Human_SNP_ID_587312029 A-to-I Human chr15 + 90475315 90475315 90475315 GCCACGACACCCGGCTTTTTTGCATTTTTAGTAGAGACGGGGGTTTCACCATGTTGGCCAGGCTG GCCACGACACCCGGCTTTTTTGCATTTTTAGTGGAGACGGGGGTTTCACCATGTTGGCCAGGCTG A G IQGAP1 Ensembl:ENSG00000140575 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1353630666 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124073,RMVar_hsa_circ_174761,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_96141,RMVar_hsa_circ_127514,RMVar_hsa_circ_174773,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_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_90067,RMVar_hsa_circ_27438,RMVar_hsa_circ_88952,RMVar_hsa_circ_174808,RMVar_hsa_circ_85108,RMVar_hsa_circ_106849,RMVar_hsa_circ_174811,RMVar_hsa_circ_174812,RMVar_hsa_circ_114375,RMVar_hsa_circ_174813,RMVar_hsa_circ_64383,RMVar_hsa_circ_84291,RMVar_hsa_circ_174814,RMVar_hsa_circ_174815,RMVar_hsa_circ_174816 37627 RMVar_ID_37627 Human_SNP_ID_587319181 A-to-I Human chr15 + 90502005 90502005 90502005 TGATGATGATATAGAATTGTGGCTTTAGTAGCACAGAGGATGCCCCAACAAACTCATGGCGTTGA TGATGATGATATAGAATTGTGGCTTTAGTAGCGCAGAGGATGCCCCAACAAACTCATGGCGTTGA A G IQGAP1 Ensembl:ENSG00000140575 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs933004111 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_467002,Human_RBP_ID_4340036,Human_RBP_ID_12635742,Human_RBP_ID_17251626,Human_RBP_ID_17689361 Human_miRNA_ID_624386 RMVar_hsa_circ_92142,RMVar_hsa_circ_174764,RMVar_hsa_circ_174769,RMVar_hsa_circ_77012,RMVar_hsa_circ_118590,RMVar_hsa_circ_127514,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_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_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_128212,RMVar_hsa_circ_174823,RMVar_hsa_circ_174826,RMVar_hsa_circ_81281,RMVar_hsa_circ_90816,RMVar_hsa_circ_174827,RMVar_hsa_circ_113201,RMVar_hsa_circ_174832,RMVar_hsa_circ_118771,RMVar_hsa_circ_174834,RMVar_hsa_circ_96955,RMVar_hsa_circ_174836,RMVar_hsa_circ_174837 37628 RMVar_ID_37628 Human_SNP_ID_587332440 A-to-I Human chr15 + 90549842 90549842 90549842 CTGCTGCCTCAGCCTCCTGAGTAGCTGAGACTACAGGCGCCTGCCACCATGCCCGGCTCATTTTT CTGCTGCCTCAGCCTCCTGAGTAGCTGAGACTCCAGGCGCCTGCCACCATGCCCGGCTCATTTTT A C CRTC3 Ensembl:ENSG00000140577 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1287326556 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_174838,RMVar_hsa_circ_75563,RMVar_hsa_circ_307272,RMVar_hsa_circ_350127,RMVar_hsa_circ_115476,RMVar_hsa_circ_174839 37629 RMVar_ID_37629 Human_SNP_ID_587349071 A-to-I Human chr15 + 90615959 90615959 90615959 CGGCTCACTGCAAACCTCCGCCTCCTGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGC CGGCTCACTGCAAACCTCCGCCTCCTGGGTTCCAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGC A C CRTC3 Ensembl:ENSG00000140577 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1004313775 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_174838,RMVar_hsa_circ_115476,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_266129,RMVar_hsa_circ_97706,RMVar_hsa_circ_174846,RMVar_hsa_circ_174847,RMVar_hsa_circ_99217,RMVar_hsa_circ_174849,RMVar_hsa_circ_118064,RMVar_hsa_circ_333159,RMVar_hsa_circ_174848,RMVar_hsa_circ_174850 37630 RMVar_ID_37630 Human_SNP_ID_587355903 A-to-I Human chr15 + 90639560 90639557 90639560 CAACCTCCACCTCCTGGGTTCAAGTGATTCTCATGTCTCAGACTCCTGAGTAATTGGGGTTACAG CAACCTCCACCTCCTGGGTTCAAGTGATTC___TGTCTCAGACTCCTGAGTAATTGGGGTTACAG CTCA C CRTC3 Ensembl:ENSG00000140577 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1162740121 Functional Loss DEL dbSNP153 31..33 33 - - - RMVar_hsa_circ_377347,RMVar_hsa_circ_174842,RMVar_hsa_circ_107780,RMVar_hsa_circ_174847,RMVar_hsa_circ_110712,RMVar_hsa_circ_174854,RMVar_hsa_circ_174858,RMVar_hsa_circ_277051 37631 RMVar_ID_37631 Human_SNP_ID_587355905 A-to-I Human chr15 + 90639560 90639560 90639560 CAACCTCCACCTCCTGGGTTCAAGTGATTCTCATGTCTCAGACTCCTGAGTAATTGGGGTTACAG CAACCTCCACCTCCTGGGTTCAAGTGATTCTCGTGTCTCAGACTCCTGAGTAATTGGGGTTACAG A G CRTC3 Ensembl:ENSG00000140577 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs998983199 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_377347,RMVar_hsa_circ_174842,RMVar_hsa_circ_107780,RMVar_hsa_circ_174847,RMVar_hsa_circ_110712,RMVar_hsa_circ_174854,RMVar_hsa_circ_174858,RMVar_hsa_circ_277051 37632 RMVar_ID_37632 Human_SNP_ID_587374065 A-to-I Human chr15 - 90705673 90705673 90705673 GCAGGCTGGTCCTGAGCTCCTGGTCTCAAGCAATCCTCCTGCCTCAGCCTCCCGAAGTGCTGGGA GCAGGCTGGTCCTGAGCTCCTGGTCTCAAGCAGTCCTCCTGCCTCAGCCTCCCGAAGTGCTGGGA T C CRTC3-AS1 Ensembl:ENSG00000259736 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1015094420 Functional Loss SNV dbSNP153 33..33 33 - - - 37633 RMVar_ID_37633 Human_SNP_ID_587374832 A-to-I Human chr15 - 90709131 90709131 90709131 TAGGCTGGAGTGCAGTGGCGCCATCTCAGCTCACTGCAACCTCTGCCTCCTGAGTTCAAGTGACT TAGGCTGGAGTGCAGTGGCGCCATCTCAGCTCGCTGCAACCTCTGCCTCCTGAGTTCAAGTGACT T C CRTC3-AS1 Ensembl:ENSG00000259736 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs932255906 Functional Loss SNV dbSNP153 33..33 33 - - - 37634 RMVar_ID_37634 Human_SNP_ID_587377662 A-to-I Human chr15 + 90720735 90720735 90720735 GGGAGTACAGGGGTGTACCACCATGCCTGGCTAATTCTTGTATTTGTTGTAGAGATGGGCTTTTG GGGAGTACAGGGGTGTACCACCATGCCTGGCTTATTCTTGTATTTGTTGTAGAGATGGGCTTTTG A T BLM Ensembl:ENSG00000197299 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs990955281 Functional Loss SNV dbSNP153 33..33 33 - - - 37635 RMVar_ID_37635 Human_SNP_ID_587386888 A-to-I Human chr15 + 90758444 90758444 90758444 GGGAAACGGAGGTTGCAGTAAGCCGACATTGCACCACTGCACTCCAGCCTGGAAGACAGAGCAAG GGGAAACGGAGGTTGCAGTAAGCCGACATTGCCCCACTGCACTCCAGCCTGGAAGACAGAGCAAG A C BLM Ensembl:ENSG00000197299 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1166080563 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25179150 RMVar_hsa_circ_47362 37636 RMVar_ID_37636 Human_SNP_ID_587387312 A-to-I Human chr15 + 90760024 90760023 90760024 GTTGCCCAGGCTGGTCTTGAACTCCTGGACTTAAGCAATCCTCCTGCCTTGGCCTCCCCAAAGGG GTTGCCCAGGCTGGTCTTGAACTCCTGGACTT_AGCAATCCTCCTGCCTTGGCCTCCCCAAAGGG TA T BLM Ensembl:ENSG00000197299 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1441698064 Functional Loss DEL dbSNP153 33..33 33 - - - Human_Splice_Rec_1644622 RMVar_hsa_circ_47362 37637 RMVar_ID_37637 Human_SNP_ID_587388572 A-to-I Human chr15 + 90764922 90764922 90764922 TGGCCAATGTCTCTACTAAAAATACAAAAATTAGCAGGATGTGGTGGTGCATGCCTATAGTCCTA TGGCCAATGTCTCTACTAAAAATACAAAAATTTGCAGGATGTGGTGGTGCATGCCTATAGTCCTA A T BLM Ensembl:ENSG00000197299 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1490521937 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47362,RMVar_hsa_circ_174859,RMVar_hsa_circ_106073,RMVar_hsa_circ_267935 37638 RMVar_ID_37638 Human_SNP_ID_587388581 A-to-I Human chr15 + 90764946 90764946 90764946 CAAAAATTAGCAGGATGTGGTGGTGCATGCCTATAGTCCTAGCTACTGGGGAGGGTAAGGCATGA CAAAAATTAGCAGGATGTGGTGGTGCATGCCTTTAGTCCTAGCTACTGGGGAGGGTAAGGCATGA A T BLM Ensembl:ENSG00000197299 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1035505036 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47362,RMVar_hsa_circ_174859,RMVar_hsa_circ_106073,RMVar_hsa_circ_267935 37639 RMVar_ID_37639 Human_SNP_ID_587394654 A-to-I Human chr15 + 90787763 90787763 90787763 CTGAGATCAAGGAGTTTGAGACCAGCCTGGCCAATATGGTGAAACCCTGTCTCTACTAAAAATAC CTGAGATCAAGGAGTTTGAGACCAGCCTGGCCCATATGGTGAAACCCTGTCTCTACTAAAAATAC A C BLM Ensembl:ENSG00000197299 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs746633299 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12638738 RMVar_hsa_circ_267935,RMVar_hsa_circ_33988,RMVar_hsa_circ_47763,RMVar_hsa_circ_323759,RMVar_hsa_circ_345902,RMVar_hsa_circ_337721 37640 RMVar_ID_37640 Human_SNP_ID_587394662 A-to-I Human chr15 + 90787785 90787785 90787785 CAGCCTGGCCAATATGGTGAAACCCTGTCTCTACTAAAAATACAAAAATTAGCCGGACGTGGTGA CAGCCTGGCCAATATGGTGAAACCCTGTCTCTGCTAAAAATACAAAAATTAGCCGGACGTGGTGA A G BLM Ensembl:ENSG00000197299 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1272881630 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267935,RMVar_hsa_circ_33988,RMVar_hsa_circ_47763,RMVar_hsa_circ_323759,RMVar_hsa_circ_345902,RMVar_hsa_circ_337721 37641 RMVar_ID_37641 Human_SNP_ID_587394663 A-to-I Human chr15 + 90787788 90787788 90787788 CCTGGCCAATATGGTGAAACCCTGTCTCTACTAAAAATACAAAAATTAGCCGGACGTGGTGATGG CCTGGCCAATATGGTGAAACCCTGTCTCTACTGAAAATACAAAAATTAGCCGGACGTGGTGATGG A G BLM Ensembl:ENSG00000197299 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1199824697 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267935,RMVar_hsa_circ_33988,RMVar_hsa_circ_47763,RMVar_hsa_circ_323759,RMVar_hsa_circ_345902,RMVar_hsa_circ_337721 37642 RMVar_ID_37642 Human_SNP_ID_587431893 A-to-I Human chr15 + 90914575 90914575 90914575 GGAGTTTCACTCTTTCGCCCAGGCTGGAGTGCAGTGGTGCAATCTCCGCTCACTGCAACCTCCGC GGAGTTTCACTCTTTCGCCCAGGCTGGAGTGCTGTGGTGCAATCTCCGCTCACTGCAACCTCCGC A T MAN2A2 Ensembl:ENSG00000196547 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs575785547 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33513,RMVar_hsa_circ_127370,RMVar_hsa_circ_34614,RMVar_hsa_circ_174880 37643 RMVar_ID_37643 Human_SNP_ID_587431897 A-to-I Human chr15 + 90914583 90914583 90914583 ACTCTTTCGCCCAGGCTGGAGTGCAGTGGTGCAATCTCCGCTCACTGCAACCTCCGCCTTCCGAT ACTCTTTCGCCCAGGCTGGAGTGCAGTGGTGCGATCTCCGCTCACTGCAACCTCCGCCTTCCGAT A G MAN2A2 Ensembl:ENSG00000196547 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1015945509 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33513,RMVar_hsa_circ_127370,RMVar_hsa_circ_34614,RMVar_hsa_circ_174880 37644 RMVar_ID_37644 Human_SNP_ID_587436208 A-to-I Human chr15 - 90930503 90930503 90930503 AAAATTAGCCGGGCGCAGTGGCTCGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA AAAATTAGCCGGGCGCAGTGGCTCGCGCCTGTCATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA T G HDDC3 Ensembl:ENSG00000184508 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1288095191 Functional Loss SNV dbSNP153 33..33 33 - - - 37645 RMVar_ID_37645 Human_SNP_ID_587440086 A-to-I Human chr15 + 90943889 90943889 90943889 TCTTGTAGTTGTAGTAGAGATAGAATCTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCT TCTTGTAGTTGTAGTAGAGATAGAATCTCACCCTGTTGGCCAGGCTGGTCTCGAACTCCTGACCT A C UNC45A Ensembl:ENSG00000140553 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs569021565 Functional Loss SNV dbSNP153 33..33 33 - - - 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 37646 RMVar_ID_37646 Human_SNP_ID_587440087 A-to-I Human chr15 + 90943889 90943889 90943889 TCTTGTAGTTGTAGTAGAGATAGAATCTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCT TCTTGTAGTTGTAGTAGAGATAGAATCTCACCGTGTTGGCCAGGCTGGTCTCGAACTCCTGACCT A G UNC45A Ensembl:ENSG00000140553 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs569021565 Functional Loss SNV dbSNP153 33..33 33 - - - 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 37647 RMVar_ID_37647 Human_SNP_ID_587440208 A-to-I Human chr15 + 90944189 90944189 90944189 TGGGCAGACCACAAGATCAGGAGTTTGAGACCAGCCTGGCCGACATGGTGAAACCCCGTCTCTAC TGGGCAGACCACAAGATCAGGAGTTTGAGACCTGCCTGGCCGACATGGTGAAACCCCGTCTCTAC A T UNC45A Ensembl:ENSG00000140553 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1050569552 Functional Loss SNV dbSNP153 33..33 33 - - - 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 37648 RMVar_ID_37648 Human_SNP_ID_587440638 A-to-I Human chr15 + 90945501 90945501 90945501 CTCCTGCTTCAGCCTCCTGAGTAGCTGGGATCACAGGCATGCACCACCACACCCAGCTAATTTTG CTCCTGCTTCAGCCTCCTGAGTAGCTGGGATCGCAGGCATGCACCACCACACCCAGCTAATTTTG A G UNC45A Ensembl:ENSG00000140553 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs183210395 Functional Loss SNV dbSNP153 33..33 33 - - - 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 37649 RMVar_ID_37649 Human_SNP_ID_587449054 A-to-I Human chr15 - 90969556 90969556 90969556 ACCCCGTACTGGCAGGCATGGAGCCAACAAGGAGAACCTGGAGCTCAACGGCAGCATCCTGAGTG ACCCCGTACTGGCAGGCATGGAGCCAACAAGGGGAACCTGGAGCTCAACGGCAGCATCCTGAGTG T C AC068831.8,PRC1 Ensembl:ENSG00000284946,Ensembl:ENSG00000198901 Protein coding,Protein coding 3'UTR,CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1175813540 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_232428,Human_RBP_ID_886037,Human_RBP_ID_1511032,Human_RBP_ID_1837130,Human_RBP_ID_3487597,Human_RBP_ID_6480253,Human_RBP_ID_8803363,Human_RBP_ID_12639612,Human_RBP_ID_18671910,Human_RBP_ID_22799711,Human_RBP_ID_22934604 Human_Splice_Rec_1645884,Human_Splice_Rec_1645890,Human_Splice_Rec_1645891,Human_Splice_Rec_1645916,Human_Splice_Rec_1645926,Human_Splice_Rec_1645932,Human_Splice_Rec_1645933,Human_Splice_Rec_1645958,Human_Splice_Rec_1645959,Human_Splice_Rec_1645970,Human_Splice_Rec_1646106,Human_Splice_Rec_1646107 RMVar_hsa_circ_75652,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_174913,RMVar_hsa_circ_174915,RMVar_hsa_circ_174916,RMVar_hsa_circ_174917,RMVar_hsa_circ_174914,RMVar_hsa_circ_44393,RMVar_hsa_circ_61093,RMVar_hsa_circ_30689 37650 RMVar_ID_37650 Human_SNP_ID_587450059 A-to-I Human chr15 - 90972364 90972364 90972364 AAATTTATTATTTTTAGACAGTGTCTTGCTCTATCACCCACACCGGAGTGCAGTGGCGCCATCAT AAATTTATTATTTTTAGACAGTGTCTTGCTCTGTCACCCACACCGGAGTGCAGTGGCGCCATCAT T C AC068831.8,PRC1 Ensembl:ENSG00000284946,Ensembl:ENSG00000198901 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs769145130 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12639703,Human_RBP_ID_23162813 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 37651 RMVar_ID_37651 Human_SNP_ID_587493213 A-to-I Human chr15 + 91131228 91131228 91131228 CCCAGGCTAGTCTTGAACTCCTGGGCTCATGCAATTCTCCTGCCCTGGCCTCCCAAAGTGTTGGG CCCAGGCTAGTCTTGAACTCCTGGGCTCATGCGATTCTCCTGCCCTGGCCTCCCAAAGTGTTGGG A G SV2B Ensembl:ENSG00000185518 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1282894242 Functional Loss SNV dbSNP153 33..33 33 - - - 37652 RMVar_ID_37652 Human_SNP_ID_587535078 A-to-I Human chr15 - 91297029 91297001 91297029 GAAGGAGCGTGCGCCCAACGATCAGGCAGAAGAAGCGTGCGCCCAACGATCGGGCAGAAGGAGCG GAAGGAGCGTGCGCCCAACGATCAGGCAGAAG____________________________GAGCG CCTTCTGCCCGATCGTTGGGCGCACGCTT C lnc-VPS33B-6,lnc-VPS33B-6:2,lnc-VPS33B-6:3 RNACentral:URS00008B374E,RNACentral:URS00008C0FC7,RNACentral:URS00008BA4FD lincRNA,lincRNA,lincRNA exon,intron,intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1417654174 Functional Loss DEL dbSNP153 33..60 33 - - - 37653 RMVar_ID_37653 Human_SNP_ID_587535098 A-to-I Human chr15 - 91297029 91297029 91297029 GAAGGAGCGTGCGCCCAACGATCAGGCAGAAGAAGCGTGCGCCCAACGATCGGGCAGAAGGAGCG GAAGGAGCGTGCGCCCAACGATCAGGCAGAAGGAGCGTGCGCCCAACGATCGGGCAGAAGGAGCG T C lnc-VPS33B-6,lnc-VPS33B-6:2,lnc-VPS33B-6:3 RNACentral:URS00008B374E,RNACentral:URS00008C0FC7,RNACentral:URS00008BA4FD lincRNA,lincRNA,lincRNA exon,intron,intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs760291557 Functional Loss SNV dbSNP153 33..33 33 - - - 37654 RMVar_ID_37654 Human_SNP_ID_587535099 A-to-I Human chr15 - 91297029 91297029 91297029 GAAGGAGCGTGCGCCCAACGATCAGGCAGAAGAAGCGTGCGCCCAACGATCGGGCAGAAGGAGCG GAAGGAGCGTGCGCCCAACGATCAGGCAGAAGCAGCGTGCGCCCAACGATCGGGCAGAAGGAGCG T G lnc-VPS33B-6,lnc-VPS33B-6:2,lnc-VPS33B-6:3 RNACentral:URS00008B374E,RNACentral:URS00008C0FC7,RNACentral:URS00008BA4FD lincRNA,lincRNA,lincRNA exon,intron,intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs760291557 Functional Loss SNV dbSNP153 33..33 33 - - - 37655 RMVar_ID_37655 Human_SNP_ID_587713573 A-to-I Human chr15 + 91969507 91969507 91969507 TTTGTATTTTTAGTAAAGTAGGGGGTTTCTCCATGTTGGCCAGGCTGGTCTCAAACTCCTCACCT TTTGTATTTTTAGTAAAGTAGGGGGTTTCTCCGTGTTGGCCAGGCTGGTCTCAAACTCCTCACCT A G SLCO3A1 Ensembl:ENSG00000176463 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1036641327 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 37656 RMVar_ID_37656 Human_SNP_ID_587714016 A-to-I Human chr15 + 91971140 91971140 91971140 GACCTTGGCCGGGCGCGGTGGCTCACACCTGTAATCTTAGCACTTCGGGAGGCCGAGGCGGGCGG GACCTTGGCCGGGCGCGGTGGCTCACACCTGTGATCTTAGCACTTCGGGAGGCCGAGGCGGGCGG A G SLCO3A1 Ensembl:ENSG00000176463 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs549669490 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 37657 RMVar_ID_37657 Human_SNP_ID_587727597 A-to-I Human chr15 + 92021408 92021408 92021408 CATGAGGGCAAGAGACTGTTTCAGAGAGAGACAAAATGAGTAAATAGCTGATGGGTGAATTCATA CATGAGGGCAAGAGACTGTTTCAGAGAGAGACGAAATGAGTAAATAGCTGATGGGTGAATTCATA A G SLCO3A1 Ensembl:ENSG00000176463 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs954912778 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 37658 RMVar_ID_37658 Human_SNP_ID_587727860 A-to-I Human chr15 + 92022539 92022539 92022539 ATTTTCTCAAAATGCATTGTTTCTGCCTTATTACAAAACGCTCGTGAGAGAAGACAGAAAGCTAA ATTTTCTCAAAATGCATTGTTTCTGCCTTATTCCAAAACGCTCGTGAGAGAAGACAGAAAGCTAA A C SLCO3A1 Ensembl:ENSG00000176463 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs546514727 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 37659 RMVar_ID_37659 Human_SNP_ID_587727895 A-to-I Human chr15 + 92022654 92022654 92022654 TTGCCTCTCTGAAACAGGTCTCTTGCCCTCACAGGGTACAGCAAGTCTGCAAACATACAGCTGAA TTGCCTCTCTGAAACAGGTCTCTTGCCCTCACGGGGTACAGCAAGTCTGCAAACATACAGCTGAA A G SLCO3A1 Ensembl:ENSG00000176463 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1292668114 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 37660 RMVar_ID_37660 Human_SNP_ID_587727926 A-to-I Human chr15 + 92022778 92022778 92022778 TAACTGCATGGTTGGTTAGGGAATGCTTTCTTAAAACAGTAGGTAACATCTGCACCAGGGCTTCA TAACTGCATGGTTGGTTAGGGAATGCTTTCTTTAAACAGTAGGTAACATCTGCACCAGGGCTTCA A T SLCO3A1 Ensembl:ENSG00000176463 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs747638645 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 37661 RMVar_ID_37661 Human_SNP_ID_587766639 A-to-I Human chr15 + 92159598 92159598 92159598 GGTTTTTTTTTTTTTTTTGGAGATAGGATCCCATTCTGTCTCCTAGCCTGGAATGCAGTGGCGTG GGTTTTTTTTTTTTTTTTGGAGATAGGATCCCTTTCTGTCTCCTAGCCTGGAATGCAGTGGCGTG A T SLCO3A1 Ensembl:ENSG00000176463 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs529266479 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_370084,RMVar_hsa_circ_174965,RMVar_hsa_circ_362572 37662 RMVar_ID_37662 Human_SNP_ID_587767512 A-to-I Human chr15 + 92162410 92162410 92162410 GATCTCAGGTGATCCACCTGCTTCAGCCTCCCAAAGTGCTGGAATTACAGGTGTGAGCCACCATG GATCTCAGGTGATCCACCTGCTTCAGCCTCCCCAAGTGCTGGAATTACAGGTGTGAGCCACCATG A C SLCO3A1 Ensembl:ENSG00000176463 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs140758091 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_370084,RMVar_hsa_circ_174965,RMVar_hsa_circ_362572 37663 RMVar_ID_37663 Human_SNP_ID_587767513 A-to-I Human chr15 + 92162410 92162410 92162410 GATCTCAGGTGATCCACCTGCTTCAGCCTCCCAAAGTGCTGGAATTACAGGTGTGAGCCACCATG GATCTCAGGTGATCCACCTGCTTCAGCCTCCCTAAGTGCTGGAATTACAGGTGTGAGCCACCATG A T SLCO3A1 Ensembl:ENSG00000176463 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs140758091 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_370084,RMVar_hsa_circ_174965,RMVar_hsa_circ_362572 37664 RMVar_ID_37664 Human_SNP_ID_587767773 A-to-I Human chr15 + 92163098 92163098 92163098 ACATAGGACAAAGTTTATCTATAACCTGGAAGACCATGAGTGGTGTGAAAACATGGAGTCCGTTT ACATAGGACAAAGTTTATCTATAACCTGGAAGCCCATGAGTGGTGTGAAAACATGGAGTCCGTTT A C SLCO3A1 Ensembl:ENSG00000176463 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs142850832 Functional Loss SNV dbSNP153 33..33 33 - - - 37665 RMVar_ID_37665 Human_SNP_ID_587767774 A-to-I Human chr15 + 92163098 92163098 92163098 ACATAGGACAAAGTTTATCTATAACCTGGAAGACCATGAGTGGTGTGAAAACATGGAGTCCGTTT ACATAGGACAAAGTTTATCTATAACCTGGAAGGCCATGAGTGGTGTGAAAACATGGAGTCCGTTT A G SLCO3A1 Ensembl:ENSG00000176463 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs142850832 Functional Loss SNV dbSNP153 33..33 33 - - - 37666 RMVar_ID_37666 Human_SNP_ID_587932947 A-to-I Human chr15 - 92781802 92781800 92781802 AAAACATTTTTATTTATTTATTTTTGAGACAGAGTATTGCTCTGTTGCCCAGGCTGGAGTGAAGT AAAACATTTTTATTTATTTATTTTTGAGACAG__TATTGCTCTGTTGCCCAGGCTGGAGTGAAGT ACT A FAM174B Ensembl:ENSG00000185442 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1236637237 Functional Loss DEL dbSNP153 33..34 33 - - - 37667 RMVar_ID_37667 Human_SNP_ID_587933842 A-to-I Human chr15 - 92784171 92784171 92784171 TTGAGCCAGGAGTTGAGACCAATCTGGGAAACATAGTGAGACCCCGTCTCTACCAAAAAAAAAAT TTGAGCCAGGAGTTGAGACCAATCTGGGAAACTTAGTGAGACCCCGTCTCTACCAAAAAAAAAAT T A FAM174B Ensembl:ENSG00000185442 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs957208358 Functional Loss SNV dbSNP153 33..33 33 - - - 37668 RMVar_ID_37668 Human_SNP_ID_587935811 A-to-I Human chr15 - 92791493 92791493 92791493 CTGCAACCTCTGCCTCCTTGGTGCAAGTGATTATATTGCCTCAGCCTCCCGAGTAACTGGGATTA CTGCAACCTCTGCCTCCTTGGTGCAAGTGATTGTATTGCCTCAGCCTCCCGAGTAACTGGGATTA T C FAM174B Ensembl:ENSG00000185442 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs769269629 Functional Loss SNV dbSNP153 33..33 33 - - - 37669 RMVar_ID_37669 Human_SNP_ID_587936606 A-to-I Human chr15 - 92794263 92794263 92794263 TGCCACCACGCCTGGCTAACTTTTGTATTTTTAGTAGAGACGGGGTTTCACAAAGTTGGCTGGGC TGCCACCACGCCTGGCTAACTTTTGTATTTTTGGTAGAGACGGGGTTTCACAAAGTTGGCTGGGC T C FAM174B Ensembl:ENSG00000185442 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1001204111 Functional Loss SNV dbSNP153 33..33 33 - - - 37670 RMVar_ID_37670 Human_SNP_ID_587936730 A-to-I Human chr15 - 92794792 92794791 92794793 TGGTTCACTGTAACTTCTGCCTCCCAGGCTCAAGTGATTCTCGTGCCTCAGCCTCCCCAGTATTT TGGTTCACTGTAACTTCTGCCTCCCAGGCTC__GTGATTCTCGTGCCTCAGCCTCCCCAGTATTT CTT C FAM174B Ensembl:ENSG00000185442 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1478568627 Functional Loss DEL dbSNP153 32..33 33 - - - 37671 RMVar_ID_37671 Human_SNP_ID_587936731 A-to-I Human chr15 - 92794792 92794792 92794792 TGGTTCACTGTAACTTCTGCCTCCCAGGCTCAAGTGATTCTCGTGCCTCAGCCTCCCCAGTATTT TGGTTCACTGTAACTTCTGCCTCCCAGGCTCAGGTGATTCTCGTGCCTCAGCCTCCCCAGTATTT T C FAM174B Ensembl:ENSG00000185442 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1407141669 Functional Loss SNV dbSNP153 33..33 33 - - - 37672 RMVar_ID_37672 Human_SNP_ID_587936732 A-to-I Human chr15 - 92794792 92794792 92794792 TGGTTCACTGTAACTTCTGCCTCCCAGGCTCAAGTGATTCTCGTGCCTCAGCCTCCCCAGTATTT TGGTTCACTGTAACTTCTGCCTCCCAGGCTCACGTGATTCTCGTGCCTCAGCCTCCCCAGTATTT T G FAM174B Ensembl:ENSG00000185442 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1407141669 Functional Loss SNV dbSNP153 33..33 33 - - - 37673 RMVar_ID_37673 Human_SNP_ID_587940022 A-to-I Human chr15 - 92806222 92806222 92806222 CCCAGGAGGCAGAGGTTGCAGTGAGCTGAGATAGTGCGACTGCACTGCAGCCTGGGCAACAGAGA CCCAGGAGGCAGAGGTTGCAGTGAGCTGAGATGGTGCGACTGCACTGCAGCCTGGGCAACAGAGA T C FAM174B,AC106028.2 Ensembl:ENSG00000185442,Ensembl:ENSG00000258922 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs920184573 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25180130 37674 RMVar_ID_37674 Human_SNP_ID_587940659 A-to-I Human chr15 - 92807543 92807543 92807543 TGGCGGGTGCTTGTAGTCCTGGAGGCTGAGGCAGGAGAATGGCGTGAACCTGGGAGGCGGAGACT TGGCGGGTGCTTGTAGTCCTGGAGGCTGAGGCTGGAGAATGGCGTGAACCTGGGAGGCGGAGACT T A FAM174B,AC106028.2 Ensembl:ENSG00000185442,Ensembl:ENSG00000258922 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1003598136 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25180132 37675 RMVar_ID_37675 Human_SNP_ID_587940660 A-to-I Human chr15 - 92807543 92807543 92807543 TGGCGGGTGCTTGTAGTCCTGGAGGCTGAGGCAGGAGAATGGCGTGAACCTGGGAGGCGGAGACT TGGCGGGTGCTTGTAGTCCTGGAGGCTGAGGCCGGAGAATGGCGTGAACCTGGGAGGCGGAGACT T G FAM174B,AC106028.2 Ensembl:ENSG00000185442,Ensembl:ENSG00000258922 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1003598136 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25180132 37676 RMVar_ID_37676 Human_SNP_ID_587965943 A-to-I Human chr15 + 92890756 92890756 92890756 CCCAGGCTGCTGGAGTGCAGTGGTGTGATCTCAACTCACTGCCACCTCCGCCTCCCGTTTTTAAG CCCAGGCTGCTGGAGTGCAGTGGTGTGATCTCGACTCACTGCCACCTCCGCCTCCCGTTTTTAAG A G LINC01578,AC013394.1 Ensembl:ENSG00000272888,Ensembl:ENSG00000279765 lincRNA,Protein coding intron,intron GSE38233;GSE107867 cultured B-cells;ASD brains,cerebellum - 24183664,30559470 RNA-Seq:(High) rs1279223182 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_288702,RMVar_hsa_circ_326458,RMVar_hsa_circ_62518,RMVar_hsa_circ_77798,RMVar_hsa_circ_174981,RMVar_hsa_circ_174982 37677 RMVar_ID_37677 Human_SNP_ID_587965962 A-to-I Human chr15 + 92890816 92890816 92890816 TTAAGTGATTATCCTGCCTTAGCCTCCTGAGTAGCTGGGATTACAGGCGTGCACCACCACACTTG TTAAGTGATTATCCTGCCTTAGCCTCCTGAGTGGCTGGGATTACAGGCGTGCACCACCACACTTG A G LINC01578,AC013394.1 Ensembl:ENSG00000272888,Ensembl:ENSG00000279765 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913485143 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_288702,RMVar_hsa_circ_326458,RMVar_hsa_circ_62518,RMVar_hsa_circ_77798,RMVar_hsa_circ_174981,RMVar_hsa_circ_174982 37678 RMVar_ID_37678 Human_SNP_ID_587966533 A-to-I Human chr15 + 92892854 92892854 92892854 GATTTATTTATTTTTATTTTATTTTTCGAGACAGAGTTCCACTGTCACCCATGCTGGAGTGCAGT GATTTATTTATTTTTATTTTATTTTTCGAGACGGAGTTCCACTGTCACCCATGCTGGAGTGCAGT A G LINC01578,AC013394.1 Ensembl:ENSG00000272888,Ensembl:ENSG00000279765 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs894033913 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6480778,Human_RBP_ID_12641380 RMVar_hsa_circ_326458,RMVar_hsa_circ_62518,RMVar_hsa_circ_77798,RMVar_hsa_circ_174982 37679 RMVar_ID_37679 Human_SNP_ID_587966873 A-to-I Human chr15 + 92893938 92893938 92893938 TTGCACAGGATGGAGTGTGGTGGCGCGATCTCAGCTCACTGCAACCCCTGCCTCCCGGGTTCAAT TTGCACAGGATGGAGTGTGGTGGCGCGATCTCGGCTCACTGCAACCCCTGCCTCCCGGGTTCAAT A G LINC01578,AC013394.1 Ensembl:ENSG00000272888,Ensembl:ENSG00000279765 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1018134888 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_326458,RMVar_hsa_circ_62518,RMVar_hsa_circ_77798,RMVar_hsa_circ_174982 37680 RMVar_ID_37680 Human_SNP_ID_587966924 A-to-I Human chr15 + 92894143 92894143 92894143 TGCTGGCCTTGGCCTCCCTAAGTGATAGGATTACAGGTGTGAGCCACCGCACCCAGCCTCTCAGG TGCTGGCCTTGGCCTCCCTAAGTGATAGGATTGCAGGTGTGAGCCACCGCACCCAGCCTCTCAGG A G LINC01578,AC013394.1 Ensembl:ENSG00000272888,Ensembl:ENSG00000279765 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1284639691 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5247030,Human_RBP_ID_25180338 RMVar_hsa_circ_326458,RMVar_hsa_circ_62518,RMVar_hsa_circ_77798,RMVar_hsa_circ_174982 37681 RMVar_ID_37681 Human_SNP_ID_587967097 A-to-I Human chr15 + 92894768 92894768 92894768 CCTGGCCCACATAGTGAAACCCCGTCTCTACTAAAATTACAAAAATTAGCCAGGCATGGTGATAT CCTGGCCCACATAGTGAAACCCCGTCTCTACTGAAATTACAAAAATTAGCCAGGCATGGTGATAT A G LINC01578,AC013394.1 Ensembl:ENSG00000272888,Ensembl:ENSG00000279765 lincRNA,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1348708533 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_326458,RMVar_hsa_circ_62518,RMVar_hsa_circ_77798,RMVar_hsa_circ_174982 37682 RMVar_ID_37682 Human_SNP_ID_587967103 A-to-I Human chr15 + 92894787 92894787 92894787 CCCCGTCTCTACTAAAATTACAAAAATTAGCCAGGCATGGTGATATGCGCCTACAGTCCCAGCTA CCCCGTCTCTACTAAAATTACAAAAATTAGCCGGGCATGGTGATATGCGCCTACAGTCCCAGCTA A G LINC01578,AC013394.1 Ensembl:ENSG00000272888,Ensembl:ENSG00000279765 lincRNA,Protein coding intron,intron GSE47997;GSE100210;GSE107867 K562 cells&HepG2 cells;HepG2 cell line;ASD brains,frontal_cortex - 23474544,29129909,30559470 RNA-Seq:(High) rs1464376195 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_326458,RMVar_hsa_circ_62518,RMVar_hsa_circ_77798,RMVar_hsa_circ_174982 37683 RMVar_ID_37683 Human_SNP_ID_587967125 A-to-I Human chr15 + 92894841 92894841 92894841 AGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGACCTGGGAGGTGCAGGTTGTGGTG AGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGGATCGCTTGACCTGGGAGGTGCAGGTTGTGGTG A G LINC01578,AC013394.1 Ensembl:ENSG00000272888,Ensembl:ENSG00000279765 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1157718938 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_326458,RMVar_hsa_circ_62518,RMVar_hsa_circ_77798,RMVar_hsa_circ_174982 37684 RMVar_ID_37684 Human_SNP_ID_587982723 A-to-I Human chr15 + 92948728 92948728 92948728 GTGGTGGCGGGCGCCTGTATGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATGGCGTGAA GTGGTGGCGGGCGCCTGTATGTAGTCCCAGCTGCTTGGGAGGCTGAGGCAGGAGAATGGCGTGAA A G CHD2,AC013394.1 Ensembl:ENSG00000173575,Ensembl:ENSG00000279765 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1032019497 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_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 37685 RMVar_ID_37685 Human_SNP_ID_587992841 A-to-I Human chr15 + 92987373 92987373 92987373 TAATCCCAGCACTTTGGGAGGCCAAGGCAGGCAGATCGCTGGAGCCTAGGAGTTTGAGACCAGCA TAATCCCAGCACTTTGGGAGGCCAAGGCAGGCGGATCGCTGGAGCCTAGGAGTTTGAGACCAGCA A G CHD2 Ensembl:ENSG00000173575 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs779052936 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74200,RMVar_hsa_circ_98654,RMVar_hsa_circ_174984,RMVar_hsa_circ_126848,RMVar_hsa_circ_362938,RMVar_hsa_circ_174986,RMVar_hsa_circ_371539,RMVar_hsa_circ_359930,RMVar_hsa_circ_88004,RMVar_hsa_circ_64882,RMVar_hsa_circ_63270,RMVar_hsa_circ_174988,RMVar_hsa_circ_174987,RMVar_hsa_circ_175001,RMVar_hsa_circ_60206,RMVar_hsa_circ_108751,RMVar_hsa_circ_65959,RMVar_hsa_circ_56143,RMVar_hsa_circ_100988,RMVar_hsa_circ_175013,RMVar_hsa_circ_88492,RMVar_hsa_circ_267267,RMVar_hsa_circ_118461,RMVar_hsa_circ_175021,RMVar_hsa_circ_175022,RMVar_hsa_circ_331496,RMVar_hsa_circ_53788,RMVar_hsa_circ_175024,RMVar_hsa_circ_175023,RMVar_hsa_circ_70647,RMVar_hsa_circ_67963,RMVar_hsa_circ_19468,RMVar_hsa_circ_72524,RMVar_hsa_circ_361437,RMVar_hsa_circ_56036,RMVar_hsa_circ_57020,RMVar_hsa_circ_117239,RMVar_hsa_circ_62934,RMVar_hsa_circ_16759,RMVar_hsa_circ_364621,RMVar_hsa_circ_175034,RMVar_hsa_circ_365470,RMVar_hsa_circ_358784,RMVar_hsa_circ_175035,RMVar_hsa_circ_175038,RMVar_hsa_circ_94734,RMVar_hsa_circ_376213,RMVar_hsa_circ_55449,RMVar_hsa_circ_175040,RMVar_hsa_circ_49614,RMVar_hsa_circ_175039,RMVar_hsa_circ_368350,RMVar_hsa_circ_70240,RMVar_hsa_circ_74275,RMVar_hsa_circ_38941,RMVar_hsa_circ_70515,RMVar_hsa_circ_119721,RMVar_hsa_circ_175041 37686 RMVar_ID_37686 Human_SNP_ID_588000220 A-to-I Human chr15 + 93015340 93015340 93015340 GCGCCATGTGATCTGCCCACCTCAGCCTCCCAAAATGTTGGGATTACAGGTGTGAACCACTGCGT GCGCCATGTGATCTGCCCACCTCAGCCTCCCAGAATGTTGGGATTACAGGTGTGAACCACTGCGT A G CHD2 Ensembl:ENSG00000173575 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1466756688 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25181304 RMVar_hsa_circ_63270,RMVar_hsa_circ_60206,RMVar_hsa_circ_72524,RMVar_hsa_circ_103601,RMVar_hsa_circ_175043,RMVar_hsa_circ_265214,RMVar_hsa_circ_364817,RMVar_hsa_circ_363894,RMVar_hsa_circ_281865,RMVar_hsa_circ_175054,RMVar_hsa_circ_378870,RMVar_hsa_circ_90289,RMVar_hsa_circ_175060 37687 RMVar_ID_37687 Human_SNP_ID_588728962 A-to-I Human chr15 + 95745882 95745882 95745882 TATCAGTTTAATATATGATACATCTTCTATCCAAGGACAATATATTAAATGGATTTTTGGAGCAG TATCAGTTTAATATATGATACATCTTCTATCCGAGGACAATATATTAAATGGATTTTTGGAGCAG A G AC015574.1,RNU2-3P Ensembl:ENSG00000275016,Ensembl:ENSG00000222076 lincRNA,snRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs185092831 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1063975,Human_RBP_ID_2462404,Human_RBP_ID_5566893,Human_RBP_ID_18199729,Human_RBP_ID_18207242,Human_RBP_ID_22799759,Human_RBP_ID_24475179,Human_RBP_ID_24551824,Human_RBP_ID_26438460,Human_RBP_ID_26748639 Human_miRNA_ID_3127527,Human_miRNA_ID_3130885 37688 RMVar_ID_37688 Human_SNP_ID_588855240 A-to-I Human chr15 - 96235122 96235122 96235122 GGCACAATCCCAGCTACTGGGGAGGCTGAGGCAGGAGAACCGCTTGAACCCTGGAGGCGGAGGTT GGCACAATCCCAGCTACTGGGGAGGCTGAGGCGGGAGAACCGCTTGAACCCTGGAGGCGGAGGTT T C NR2F2-AS1 Ensembl:ENSG00000247809 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs564975780 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_175085,RMVar_hsa_circ_344872 37689 RMVar_ID_37689 Human_SNP_ID_588985849 A-to-I Human chr15 + 96757244 96757244 96757244 ACAGGCGCAGGGATATCTACTGAAGGCAACTCAGACTTCTCCTGGGAATATGGTGAACTCGATCA ACAGGCGCAGGGATATCTACTGAAGGCAACTCCGACTTCTCCTGGGAATATGGTGAACTCGATCA A C FAM149B1P1 Ensembl:ENSG00000214424 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1192698234 Functional Loss SNV dbSNP153 33..33 33 - - - 37690 RMVar_ID_37690 Human_SNP_ID_589513504 A-to-I Human chr15 + 98751011 98751011 98751011 CAGGGTTTCATCATGTTGCCCAGGCTCATCTCAAACTCCTGGCCTCAAGTGATCCACCCACCTCG CAGGGTTTCATCATGTTGCCCAGGCTCATCTCTAACTCCTGGCCTCAAGTGATCCACCCACCTCG A T IGF1R Ensembl:ENSG00000140443 Protein coding intron GSE107867 ASD brains,cerebellum;ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1037386485 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 37691 RMVar_ID_37691 Human_SNP_ID_589514812 A-to-I Human chr15 + 98755485 98755485 98755485 ATTGCTGGCTGGGCATGGTGGCTCATGCCTGTAATCCCGGCAATTTGGGAGGCTGAAGTGGGTGG ATTGCTGGCTGGGCATGGTGGCTCATGCCTGTGATCCCGGCAATTTGGGAGGCTGAAGTGGGTGG A G IGF1R Ensembl:ENSG00000140443 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1417067047 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22473476 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 37692 RMVar_ID_37692 Human_SNP_ID_589556877 A-to-I Human chr15 + 98905302 98905302 98905302 AATAAACATTTTTTACAACATAGAGAAGGCTGAGAACCAGGATACCAATATCAATAAAATCTGGA AATAAACATTTTTTACAACATAGAGAAGGCTGGGAACCAGGATACCAATATCAATAAAATCTGGA A G IGF1R Ensembl:ENSG00000140443 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1173323992 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12520,RMVar_hsa_circ_175102,RMVar_hsa_circ_318859,RMVar_hsa_circ_372350,RMVar_hsa_circ_373683,RMVar_hsa_circ_326921,RMVar_hsa_circ_125337,RMVar_hsa_circ_175103,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_111531,RMVar_hsa_circ_175114,RMVar_hsa_circ_175115,RMVar_hsa_circ_57443,RMVar_hsa_circ_52470,RMVar_hsa_circ_175117,RMVar_hsa_circ_32268 37693 RMVar_ID_37693 Human_SNP_ID_589617124 A-to-I Human chr15 + 99110230 99110230 99110230 TTCCTTGTTTTACGTGGCATTTTTCACTGCTGAATCCGCAGCCATGAAGAACTGCGCTTGGCACA TTCCTTGTTTTACGTGGCATTTTTCACTGCTGGATCCGCAGCCATGAAGAACTGCGCTTGGCACA A G SYNM Ensembl:ENSG00000182253 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1165619437 Functional Loss SNV dbSNP153 33..33 33 - - - 37694 RMVar_ID_37694 Human_SNP_ID_589617127 A-to-I Human chr15 + 99110237 99110237 99110237 TTTTACGTGGCATTTTTCACTGCTGAATCCGCAGCCATGAAGAACTGCGCTTGGCACACTAAATG TTTTACGTGGCATTTTTCACTGCTGAATCCGCTGCCATGAAGAACTGCGCTTGGCACACTAAATG A T SYNM Ensembl:ENSG00000182253 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1186502814 Functional Loss SNV dbSNP153 33..33 33 - - - 37695 RMVar_ID_37695 Human_SNP_ID_589617130 A-to-I Human chr15 + 99110244 99110244 99110244 TGGCATTTTTCACTGCTGAATCCGCAGCCATGAAGAACTGCGCTTGGCACACTAAATGCTCAACG TGGCATTTTTCACTGCTGAATCCGCAGCCATGTAGAACTGCGCTTGGCACACTAAATGCTCAACG A T SYNM Ensembl:ENSG00000182253 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1184276962 Functional Loss SNV dbSNP153 33..33 33 - - - 37696 RMVar_ID_37696 Human_SNP_ID_589617141 A-to-I Human chr15 + 99110300 99110300 99110300 TGCTCAACGGCTGGTAGTTGAACGAATGAACCAATTGTATACACCCTGGGAGCTACTTCCGGTAC TGCTCAACGGCTGGTAGTTGAACGAATGAACCCATTGTATACACCCTGGGAGCTACTTCCGGTAC A C SYNM Ensembl:ENSG00000182253 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs920625650 Functional Loss SNV dbSNP153 33..33 33 - - - 37697 RMVar_ID_37697 Human_SNP_ID_589617549 A-to-I Human chr15 + 99111889 99111889 99111889 CAACGTGGTGAAACCCCGTCTCTACTAACAATACAAAAATCAGTTGGGCGTGATGGCAGGCGCCT CAACGTGGTGAAACCCCGTCTCTACTAACAATGCAAAAATCAGTTGGGCGTGATGGCAGGCGCCT A G SYNM Ensembl:ENSG00000182253 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1360938897 Functional Loss SNV dbSNP153 33..33 33 - - - 37698 RMVar_ID_37698 Human_SNP_ID_589638444 A-to-I Human chr15 - 99193820 99193820 99193820 ATCTTTGAGTAGAGATGGGGTTTCACTATGTTAGCCAGGCTGGTCTTGAACTCTTGACCTCAAGT ATCTTTGAGTAGAGATGGGGTTTCACTATGTTGGCCAGGCTGGTCTTGAACTCTTGACCTCAAGT T C TTC23 Ensembl:ENSG00000103852 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1021795689 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82978,RMVar_hsa_circ_15147,RMVar_hsa_circ_124920,RMVar_hsa_circ_175139,RMVar_hsa_circ_266999,RMVar_hsa_circ_74121,RMVar_hsa_circ_175140,RMVar_hsa_circ_64152 37699 RMVar_ID_37699 Human_SNP_ID_589654489 A-to-I Human chr15 - 99257695 99257695 99257695 CTTCTACTGTACCTTCCACATCAACTTCATCAACAGCTCTGACCGACCCGAAGGTCAGCAGGACG CTTCTACTGTACCTTCCACATCAACTTCATCATCAGCTCTGACCGACCCGAAGGTCAGCAGGACG T A - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs878940719 Functional Loss SNV dbSNP153 33..33 33 - - - 37700 RMVar_ID_37700 Human_SNP_ID_589654490 A-to-I Human chr15 - 99257696 99257696 99257696 TCTTCTACTGTACCTTCCACATCAACTTCATCAACAGCTCTGACCGACCCGAAGGTCAGCAGGAC TCTTCTACTGTACCTTCCACATCAACTTCATCGACAGCTCTGACCGACCCGAAGGTCAGCAGGAC T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs878933727 Functional Loss SNV dbSNP153 33..33 33 - - - 37701 RMVar_ID_37701 Human_SNP_ID_589654701 A-to-I Human chr15 + 99258487 99258487 99258487 TTTATGTATGGAGCAGCAAGACTGAAACTGTTAAGGAGCCATGAAGGAAGAAGCAGCAGCAAAAG TTTATGTATGGAGCAGCAAGACTGAAACTGTTGAGGAGCCATGAAGGAAGAAGCAGCAGCAAAAG A G HSP90B2P,LRRC28 Ensembl:ENSG00000259706,Ensembl:ENSG00000168904 Pseudogene,Protein coding exon,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs879142326 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3490221,Human_RBP_ID_5096311,Human_RBP_ID_5247007,Human_RBP_ID_5567762,Human_RBP_ID_8251376,Human_RBP_ID_17367738,Human_RBP_ID_17484737,Human_RBP_ID_22388407 Human_miRNA_ID_1839309 RMVar_hsa_circ_353891,RMVar_hsa_circ_369034,RMVar_hsa_circ_369035,RMVar_hsa_circ_357147,RMVar_hsa_circ_175142,RMVar_hsa_circ_349426 37702 RMVar_ID_37702 Human_SNP_ID_589654732 A-to-I Human chr15 - 99258611 99258611 99258611 ATTGGTTTGATATCATTCATAAGTTCCCATTCACAGACAGTTTTTTCAACTTTTTTAGTCTTTGG ATTGGTTTGATATCATTCATAAGTTCCCATTCCCAGACAGTTTTTTCAACTTTTTTAGTCTTTGG T G - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs879204740 Functional Loss SNV dbSNP153 33..33 33 - - - 37703 RMVar_ID_37703 Human_SNP_ID_589654940 A-to-I Human chr15 + 99259522 99259522 99259522 GCCATTAAGGACAAGATTGAAAAGGCTATGGTATCTCAGTGCCTGACAGAATCTCTGTGTGCTTT GCCATTAAGGACAAGATTGAAAAGGCTATGGTGTCTCAGTGCCTGACAGAATCTCTGTGTGCTTT A G HSP90B2P,LRRC28 Ensembl:ENSG00000259706,Ensembl:ENSG00000168904 Pseudogene,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878915225 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5567767 RMVar_hsa_circ_353891,RMVar_hsa_circ_369034,RMVar_hsa_circ_369035,RMVar_hsa_circ_357147,RMVar_hsa_circ_175142,RMVar_hsa_circ_349426 37704 RMVar_ID_37704 Human_SNP_ID_589654942 A-to-I Human chr15 - 99259529 99259529 99259529 GGCCACCAAAGCACACAGAGATTCTGTCAGGCACTGAGATACCATAGCCTTTTCAATCTTGTCCT GGCCACCAAAGCACACAGAGATTCTGTCAGGCGCTGAGATACCATAGCCTTTTCAATCTTGTCCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879090981 Functional Loss SNV dbSNP153 33..33 33 - - - 37705 RMVar_ID_37705 Human_SNP_ID_589663021 A-to-I Human chr15 + 99290892 99290892 99290892 GGGAGGCTGGGGCGGGAGAATCTCTTGAGCCCAGGATATCAAGGGCTGCAGTGAACTCTGATTGC GGGAGGCTGGGGCGGGAGAATCTCTTGAGCCCGGGATATCAAGGGCTGCAGTGAACTCTGATTGC A G LRRC28 Ensembl:ENSG00000168904 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs994124007 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61679,RMVar_hsa_circ_353891,RMVar_hsa_circ_369034,RMVar_hsa_circ_369035,RMVar_hsa_circ_357147,RMVar_hsa_circ_175142,RMVar_hsa_circ_357749,RMVar_hsa_circ_360963,RMVar_hsa_circ_175145,RMVar_hsa_circ_287148,RMVar_hsa_circ_340268,RMVar_hsa_circ_356149,RMVar_hsa_circ_175148,RMVar_hsa_circ_175149,RMVar_hsa_circ_175147 37706 RMVar_ID_37706 Human_SNP_ID_589740939 A-to-I Human chr15 + 99596079 99596079 99596079 TCTCATTACAGATTATTGTAAAATAACTATAAAAACTTGATTTTTTACAGTATTGTCTTTTAGAA TCTCATTACAGATTATTGTAAAATAACTATAAGAACTTGATTTTTTACAGTATTGTCTTTTAGAA A G MEF2A Ensembl:ENSG00000068305 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1036734625 Functional Loss SNV dbSNP153 33..33 33 - - - 37707 RMVar_ID_37707 Human_SNP_ID_589755265 A-to-I Human chr15 + 99652334 99652334 99652334 CTCGTGCAGTTCGCAGTAGGTTTCATTCTCTTACGAGAATCCAATGCTGCTGCTGATGTGACGGG CTCGTGCAGTTCGCAGTAGGTTTCATTCTCTTGCGAGAATCCAATGCTGCTGCTGATGTGACGGG A G MEF2A Ensembl:ENSG00000068305 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1326590367 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_289273,RMVar_hsa_circ_307817,RMVar_hsa_circ_367559,RMVar_hsa_circ_175156,RMVar_hsa_circ_175154,RMVar_hsa_circ_175155,RMVar_hsa_circ_325751,RMVar_hsa_circ_325605,RMVar_hsa_circ_350879,RMVar_hsa_circ_316550,RMVar_hsa_circ_285255,RMVar_hsa_circ_294606,RMVar_hsa_circ_329410,RMVar_hsa_circ_175157 37708 RMVar_ID_37708 Human_SNP_ID_589757865 A-to-I Human chr15 + 99663091 99663091 99663091 ATAAAGTTGAGCGTATGTTAATTTTTTTTTTCAGTTCTTGGTAGGCAGGAGTTAAAAGTGCAGGC ATAAAGTTGAGCGTATGTTAATTTTTTTTTTCTGTTCTTGGTAGGCAGGAGTTAAAAGTGCAGGC A T MEF2A Ensembl:ENSG00000068305 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1464624281 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_289273,RMVar_hsa_circ_307817,RMVar_hsa_circ_367559,RMVar_hsa_circ_175156,RMVar_hsa_circ_175154,RMVar_hsa_circ_175155,RMVar_hsa_circ_325751,RMVar_hsa_circ_325605,RMVar_hsa_circ_350879,RMVar_hsa_circ_316550,RMVar_hsa_circ_175158,RMVar_hsa_circ_285255,RMVar_hsa_circ_294606,RMVar_hsa_circ_329410,RMVar_hsa_circ_175157 37709 RMVar_ID_37709 Human_SNP_ID_589759173 A-to-I Human chr15 + 99667484 99667484 99667484 TGACCTCGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTCAGCCACCGCGC TGACCTCGTGATCCGCCCGCCTCGGCCTCCCAGAGTGCTGGGATTACAGGCGTCAGCCACCGCGC A G MEF2A Ensembl:ENSG00000068305 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042538307 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_289273,RMVar_hsa_circ_307817,RMVar_hsa_circ_367559,RMVar_hsa_circ_175156,RMVar_hsa_circ_175154,RMVar_hsa_circ_175155,RMVar_hsa_circ_325751,RMVar_hsa_circ_325605,RMVar_hsa_circ_350879,RMVar_hsa_circ_316550,RMVar_hsa_circ_175158,RMVar_hsa_circ_285255,RMVar_hsa_circ_294606,RMVar_hsa_circ_329410,RMVar_hsa_circ_175157,RMVar_hsa_circ_175159 37710 RMVar_ID_37710 Human_SNP_ID_589761524 A-to-I Human chr15 + 99676687 99676687 99676687 CTTCACCTCCCGGGTTCACGCCATTCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGTGCCCG CTTCACCTCCCGGGTTCACGCCATTCTGCCTCCGCCTCCCGAGTAGCTGGGACTACAGGTGCCCG A C MEF2A Ensembl:ENSG00000068305 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs965193076 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_289273,RMVar_hsa_circ_367559,RMVar_hsa_circ_94591,RMVar_hsa_circ_175155,RMVar_hsa_circ_325751,RMVar_hsa_circ_350879,RMVar_hsa_circ_316550,RMVar_hsa_circ_294606,RMVar_hsa_circ_297528,RMVar_hsa_circ_337436,RMVar_hsa_circ_55518,RMVar_hsa_circ_175160,RMVar_hsa_circ_175161,RMVar_hsa_circ_328371,RMVar_hsa_circ_368274,RMVar_hsa_circ_76277,RMVar_hsa_circ_175164 37711 RMVar_ID_37711 Human_SNP_ID_589766095 A-to-I Human chr15 + 99694532 99694525 99694532 TGCTCAACAGGTTTTAGATCTTGGAGCATTTCAGATTTCAGATTTTCAGATTTGGGATGACCAAC TGCTCAACAGGTTTTAGATCTTGGAG_______GATTTCAGATTTTCAGATTTGGGATGACCAAC GCATTTCA G MEF2A Ensembl:ENSG00000068305 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1378319304 Functional Loss DEL dbSNP153 27..33 33 - - - Human_RBP_ID_18660111 RMVar_hsa_circ_289273,RMVar_hsa_circ_94591,RMVar_hsa_circ_325751,RMVar_hsa_circ_350879,RMVar_hsa_circ_297528,RMVar_hsa_circ_55518,RMVar_hsa_circ_175160,RMVar_hsa_circ_368274,RMVar_hsa_circ_76277,RMVar_hsa_circ_175164,RMVar_hsa_circ_39839 37712 RMVar_ID_37712 Human_SNP_ID_589766096 A-to-I Human chr15 + 99694532 99694526 99694533 TGCTCAACAGGTTTTAGATCTTGGAGCATTTCAGATTTCAGATTTTCAGATTTGGGATGACCAAC TGCTCAACAGGTTTTAGATCTTGGAGC_______ATTTCAGATTTTCAGATTTGGGATGACCAAC CATTTCAG C MEF2A Ensembl:ENSG00000068305 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1181353551 Functional Loss DEL dbSNP153 28..34 33 - - - Human_RBP_ID_18660111 RMVar_hsa_circ_289273,RMVar_hsa_circ_94591,RMVar_hsa_circ_325751,RMVar_hsa_circ_350879,RMVar_hsa_circ_297528,RMVar_hsa_circ_55518,RMVar_hsa_circ_175160,RMVar_hsa_circ_368274,RMVar_hsa_circ_76277,RMVar_hsa_circ_175164,RMVar_hsa_circ_39839 37713 RMVar_ID_37713 Human_SNP_ID_589766167 A-to-I Human chr15 + 99694816 99694816 99694816 CTTCTGCACGGGAGATTTATCTCTTCTCTCTCATTTATTCAACCATTTATTTCTATCAATATGGA CTTCTGCACGGGAGATTTATCTCTTCTCTCTCCTTTATTCAACCATTTATTTCTATCAATATGGA A C MEF2A Ensembl:ENSG00000068305 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1267011130 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2433738 RMVar_hsa_circ_289273,RMVar_hsa_circ_94591,RMVar_hsa_circ_325751,RMVar_hsa_circ_350879,RMVar_hsa_circ_297528,RMVar_hsa_circ_55518,RMVar_hsa_circ_175160,RMVar_hsa_circ_368274,RMVar_hsa_circ_76277,RMVar_hsa_circ_175164,RMVar_hsa_circ_39839 37714 RMVar_ID_37714 Human_SNP_ID_589768104 A-to-I Human chr15 + 99701354 99701354 99701354 GAAAATCAGACCCAAATTGAGAGACATTCTATAAGATAACTGATCAGCACTCTTTCAAAACAAGT GAAAATCAGACCCAAATTGAGAGACATTCTATGAGATAACTGATCAGCACTCTTTCAAAACAAGT A G MEF2A Ensembl:ENSG00000068305 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1331715306 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_289273,RMVar_hsa_circ_94591,RMVar_hsa_circ_325751,RMVar_hsa_circ_350879,RMVar_hsa_circ_297528,RMVar_hsa_circ_55518,RMVar_hsa_circ_175160,RMVar_hsa_circ_368274,RMVar_hsa_circ_76277,RMVar_hsa_circ_175164,RMVar_hsa_circ_39839 37715 RMVar_ID_37715 Human_SNP_ID_589768125 A-to-I Human chr15 + 99701437 99701434 99701438 CAAGTTGTCAAGGTCATGAAAAGGAAAGACTGAGGAACTGTCACAGAGCAGAGGAGACGAAGGAG CAAGTTGTCAAGGTCATGAAAAGGAAAGAC____GAACTGTCACAGAGCAGAGGAGACGAAGGAG CTGAG C MEF2A Ensembl:ENSG00000068305 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1209728330 Functional Loss DEL dbSNP153 31..34 33 - - - RMVar_hsa_circ_289273,RMVar_hsa_circ_94591,RMVar_hsa_circ_325751,RMVar_hsa_circ_350879,RMVar_hsa_circ_297528,RMVar_hsa_circ_55518,RMVar_hsa_circ_175160,RMVar_hsa_circ_368274,RMVar_hsa_circ_76277,RMVar_hsa_circ_175164,RMVar_hsa_circ_39839 37716 RMVar_ID_37716 Human_SNP_ID_590012912 A-to-I Human chr15 + 100553787 100553787 100553787 GTTCTGTCAACCACGAGCAGTTTCTTAATGAGATCTTTCACATGGAAATCCAAATGTCTGGGGAA GTTCTGTCAACCACGAGCAGTTTCTTAATGAGCTCTTTCACATGGAAATCCAAATGTCTGGGGAA A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1396226846 Functional Loss SNV dbSNP153 33..33 33 - - - 37717 RMVar_ID_37717 Human_SNP_ID_590012913 A-to-I Human chr15 + 100553787 100553787 100553787 GTTCTGTCAACCACGAGCAGTTTCTTAATGAGATCTTTCACATGGAAATCCAAATGTCTGGGGAA GTTCTGTCAACCACGAGCAGTTTCTTAATGAGTTCTTTCACATGGAAATCCAAATGTCTGGGGAA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1396226846 Functional Loss SNV dbSNP153 33..33 33 - - - 37718 RMVar_ID_37718 Human_SNP_ID_590139406 A-to-I Human chr15 + 101029793 101029793 101029793 GGGAGACTGAAGCAGGAGAATTGCTTGAACCCAGGAGGCAGAGGTTGCAGTGAACAGAGATCACA GGGAGACTGAAGCAGGAGAATTGCTTGAACCCGGGAGGCAGAGGTTGCAGTGAACAGAGATCACA A G LRRK1 Ensembl:ENSG00000154237 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs979889814 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118622,RMVar_hsa_circ_82290,RMVar_hsa_circ_175205,RMVar_hsa_circ_121411,RMVar_hsa_circ_119669,RMVar_hsa_circ_101102,RMVar_hsa_circ_175210,RMVar_hsa_circ_175208,RMVar_hsa_circ_175209,RMVar_hsa_circ_175207 37719 RMVar_ID_37719 Human_SNP_ID_590145502 A-to-I Human chr15 + 101054078 101054078 101054078 TCAGCTCACTGCAGCTTTGACCTCCTGAACTCAAGCCATCCTCCCACCGCAACTTCCCGAGTAGC TCAGCTCACTGCAGCTTTGACCTCCTGAACTCGAGCCATCCTCCCACCGCAACTTCCCGAGTAGC A G LRRK1 Ensembl:ENSG00000154237 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1255451282 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82290,RMVar_hsa_circ_119669,RMVar_hsa_circ_101102,RMVar_hsa_circ_175208,RMVar_hsa_circ_175209,RMVar_hsa_circ_175207 37720 RMVar_ID_37720 Human_SNP_ID_590145515 A-to-I Human chr15 + 101054114 101054114 101054114 CATCCTCCCACCGCAACTTCCCGAGTAGCTACAAGCACACGCCACCACACCCAGCTAATTTGTTG CATCCTCCCACCGCAACTTCCCGAGTAGCTACCAGCACACGCCACCACACCCAGCTAATTTGTTG A C LRRK1 Ensembl:ENSG00000154237 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs141216952 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82290,RMVar_hsa_circ_119669,RMVar_hsa_circ_101102,RMVar_hsa_circ_175208,RMVar_hsa_circ_175209,RMVar_hsa_circ_175207 37721 RMVar_ID_37721 Human_SNP_ID_590192189 A-to-I Human chr15 + 101216954 101216954 101216954 AGGATGGAATGCAGAGTGTGACAAAACAATCTAACTGCATTACAAATGTATGAGACAATCTCACT AGGATGGAATGCAGAGTGTGACAAAACAATCTGACTGCATTACAAATGTATGAGACAATCTCACT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559550248 Functional Loss SNV dbSNP153 33..33 33 - - - 37722 RMVar_ID_37722 Human_SNP_ID_590211547 A-to-I Human chr15 - 101283359 101283359 101283359 TAGAGACAGGGTTTCTACTAAAAACACATGTTAGCCAGGATGGTCTCGATCTCCTGACCTCATGA TAGAGACAGGGTTTCTACTAAAAACACATGTTGGCCAGGATGGTCTCGATCTCCTGACCTCATGA T C SNRPA1 Ensembl:ENSG00000131876 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs1305374717 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12478045,Human_RBP_ID_25184478 RMVar_hsa_circ_115260,RMVar_hsa_circ_109518,RMVar_hsa_circ_175225,RMVar_hsa_circ_175227,RMVar_hsa_circ_79442,RMVar_hsa_circ_175226 37723 RMVar_ID_37723 Human_SNP_ID_590211603 A-to-I Human chr15 - 101283519 101283519 101283519 CTCTGTCGCCCAGGCTATAGGGCAGTGGTGCAATCTCACCTCACTGCAAGCTCCGCCTCCTGGGT CTCTGTCGCCCAGGCTATAGGGCAGTGGTGCAGTCTCACCTCACTGCAAGCTCCGCCTCCTGGGT T C SNRPA1 Ensembl:ENSG00000131876 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs754389816 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12478046 RMVar_hsa_circ_115260,RMVar_hsa_circ_109518,RMVar_hsa_circ_175225,RMVar_hsa_circ_175227,RMVar_hsa_circ_79442,RMVar_hsa_circ_175226 37724 RMVar_ID_37724 Human_SNP_ID_590211743 A-to-I Human chr15 - 101283914 101283914 101283914 CTTTTTGAGTCGGAGTTTTGCTCTTTTTGCCCAGGCTGGAGTGCAGTGGCGCGATCTCGGCTCAC CTTTTTGAGTCGGAGTTTTGCTCTTTTTGCCCCGGCTGGAGTGCAGTGGCGCGATCTCGGCTCAC T G SNRPA1 Ensembl:ENSG00000131876 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs975280031 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115260,RMVar_hsa_circ_109518,RMVar_hsa_circ_175225,RMVar_hsa_circ_175227,RMVar_hsa_circ_79442,RMVar_hsa_circ_175226 37725 RMVar_ID_37725 Human_SNP_ID_590213114 A-to-I Human chr15 - 101288490 101288490 101288490 TAATCCCAGCTCTTTGGGAGGCCGAGGCAGGCAGATCACGAGGTCAGGAGATCGAGACCATCGTG TAATCCCAGCTCTTTGGGAGGCCGAGGCAGGCGGATCACGAGGTCAGGAGATCGAGACCATCGTG T C SNRPA1 Ensembl:ENSG00000131876 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1214074956 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25129801 RMVar_hsa_circ_109518,RMVar_hsa_circ_175227,RMVar_hsa_circ_79442,RMVar_hsa_circ_175226,RMVar_hsa_circ_17181 37726 RMVar_ID_37726 Human_SNP_ID_590213117 A-to-I Human chr15 - 101288494 101288494 101288494 CCTGTAATCCCAGCTCTTTGGGAGGCCGAGGCAGGCAGATCACGAGGTCAGGAGATCGAGACCAT CCTGTAATCCCAGCTCTTTGGGAGGCCGAGGCGGGCAGATCACGAGGTCAGGAGATCGAGACCAT T C SNRPA1 Ensembl:ENSG00000131876 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1195596465 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109518,RMVar_hsa_circ_175227,RMVar_hsa_circ_79442,RMVar_hsa_circ_175226,RMVar_hsa_circ_17181 37727 RMVar_ID_37727 Human_SNP_ID_590213125 A-to-I Human chr15 - 101288520 101288520 101288520 CTGCCCACTGGGCGTGGTGGCTCACGCCTGTAATCCCAGCTCTTTGGGAGGCCGAGGCAGGCAGA CTGCCCACTGGGCGTGGTGGCTCACGCCTGTAGTCCCAGCTCTTTGGGAGGCCGAGGCAGGCAGA T C SNRPA1 Ensembl:ENSG00000131876 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1165360442 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109518,RMVar_hsa_circ_175227,RMVar_hsa_circ_79442,RMVar_hsa_circ_175226,RMVar_hsa_circ_17181 37728 RMVar_ID_37728 Human_SNP_ID_590214644 A-to-I Human chr15 - 101294051 101294051 101294051 TTTTGTATTTTTAGTAAAGACATGGTTTCTCCATGTTGGTCAGGCTGGTCTCGAACTCCCGACCT TTTTGTATTTTTAGTAAAGACATGGTTTCTCCGTGTTGGTCAGGCTGGTCTCGAACTCCCGACCT T C SNRPA1 Ensembl:ENSG00000131876 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs887473829 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25129905 RMVar_hsa_circ_109518,RMVar_hsa_circ_175227 37729 RMVar_ID_37729 Human_SNP_ID_590220469 A-to-I Human chr15 + 101314647 101314646 101314647 GGGCTGGCTTCACACCTCAGAACCACAGCCGTAAGCCTGGGAGGGAATTCTGAGCTCCTGCAGGA GGGCTGGCTTCACACCTCAGAACCACAGCCGT_AGCCTGGGAGGGAATTCTGAGCTCCTGCAGGA TA T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1441152245 Functional Loss DEL dbSNP153 33..33 33 - - - 37730 RMVar_ID_37730 Human_SNP_ID_590320944 A-to-I Human chr15 - 101684086 101684086 101684086 GCTTCCAGCAGGACGATGCTCACATTTTTTGCACAGTGGAGCAGGTAAACAATAACACAGAGTGA GCTTCCAGCAGGACGATGCTCACATTTTTTGCCCAGTGGAGCAGGTAAACAATAACACAGAGTGA T G TARS3 Ensembl:ENSG00000185418 Protein coding CDS GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs1275436450 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1651879,Human_Splice_Rec_1651907,Human_Splice_Rec_1651941,Human_Splice_Rec_1651985 Human_miRNA_ID_516185,Human_miRNA_ID_520412,Human_miRNA_ID_2181290,Human_miRNA_ID_2183394,Human_miRNA_ID_2969290 RMVar_hsa_circ_50524,RMVar_hsa_circ_268013,RMVar_hsa_circ_333228,RMVar_hsa_circ_371522,RMVar_hsa_circ_315163,RMVar_hsa_circ_766,RMVar_hsa_circ_30966,RMVar_hsa_circ_175253,RMVar_hsa_circ_175254,RMVar_hsa_circ_323748,RMVar_hsa_circ_53466,RMVar_hsa_circ_69998,RMVar_hsa_circ_175256,RMVar_hsa_circ_306341,RMVar_hsa_circ_45908,RMVar_hsa_circ_175257,RMVar_hsa_circ_34530,RMVar_hsa_circ_306436,RMVar_hsa_circ_344750,RMVar_hsa_circ_175258 37731 RMVar_ID_37731 Human_SNP_ID_590326672 A-to-I Human chr15 - 101706187 101706187 101706187 GGTCAGGAGTTTGAGACCAGCCTGGCCAACATAGTGAAACCCTGTCTCTACTAAAAATACAAAAA GGTCAGGAGTTTGAGACCAGCCTGGCCAACATGGTGAAACCCTGTCTCTACTAAAAATACAAAAA T C TARS3 Ensembl:ENSG00000185418 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1416911520 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_371522,RMVar_hsa_circ_766,RMVar_hsa_circ_30966,RMVar_hsa_circ_175253,RMVar_hsa_circ_45908,RMVar_hsa_circ_344750,RMVar_hsa_circ_98532,RMVar_hsa_circ_175260,RMVar_hsa_circ_303057,RMVar_hsa_circ_276639,RMVar_hsa_circ_126114,RMVar_hsa_circ_59605,RMVar_hsa_circ_175262,RMVar_hsa_circ_175263,RMVar_hsa_circ_175261,RMVar_hsa_circ_97113,RMVar_hsa_circ_175268,RMVar_hsa_circ_286156,RMVar_hsa_circ_175269 37732 RMVar_ID_37732 Human_SNP_ID_590326679 A-to-I Human chr15 - 101706215 101706215 101706215 GGGAGGCCAAGGCAGGCGGATCACTAGAGGTCAGGAGTTTGAGACCAGCCTGGCCAACATAGTGA GGGAGGCCAAGGCAGGCGGATCACTAGAGGTCGGGAGTTTGAGACCAGCCTGGCCAACATAGTGA T C TARS3 Ensembl:ENSG00000185418 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs900645490 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_371522,RMVar_hsa_circ_766,RMVar_hsa_circ_30966,RMVar_hsa_circ_175253,RMVar_hsa_circ_45908,RMVar_hsa_circ_344750,RMVar_hsa_circ_98532,RMVar_hsa_circ_175260,RMVar_hsa_circ_303057,RMVar_hsa_circ_276639,RMVar_hsa_circ_126114,RMVar_hsa_circ_59605,RMVar_hsa_circ_175262,RMVar_hsa_circ_175263,RMVar_hsa_circ_175261,RMVar_hsa_circ_97113,RMVar_hsa_circ_175268,RMVar_hsa_circ_286156,RMVar_hsa_circ_175269 37733 RMVar_ID_37733 Human_SNP_ID_590327130 A-to-I Human chr15 - 101708078 101708076 101708079 CCGTGCCTGACTAATTTTTCTATCCTTTTAGTAGAGACAAAGTTTTGCCATGTTGGCCAGGCTGG CCGTGCCTGACTAATTTTTCTATCCTTTTAG___AGACAAAGTTTTGCCATGTTGGCCAGGCTGG TCTA T TARS3 Ensembl:ENSG00000185418 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1330859434 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_371522,RMVar_hsa_circ_766,RMVar_hsa_circ_30966,RMVar_hsa_circ_175253,RMVar_hsa_circ_45908,RMVar_hsa_circ_344750,RMVar_hsa_circ_98532,RMVar_hsa_circ_175260,RMVar_hsa_circ_303057,RMVar_hsa_circ_276639,RMVar_hsa_circ_126114,RMVar_hsa_circ_59605,RMVar_hsa_circ_175262,RMVar_hsa_circ_175263,RMVar_hsa_circ_175261,RMVar_hsa_circ_97113,RMVar_hsa_circ_175268,RMVar_hsa_circ_286156,RMVar_hsa_circ_175269 37734 RMVar_ID_37734 Human_SNP_ID_590400502 A-to-I Human chr15 + 101972594 101972594 101972594 CTGTGATCTTCTCCATGGCAGGATCTCCCAGCAGGTAGAGCAGAGCCGGAGCCAGGTGCAGGCCA CTGTGATCTTCTCCATGGCAGGATCTCCCAGCGGGTAGAGCAGAGCCGGAGCCAGGTGCAGGCCA A G WASH3P Ensembl:ENSG00000185596 Pseudogene intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1352586735 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5567305 Human_Splice_Rec_1652120,Human_Splice_Rec_1652156 Human_miRNA_ID_1855537,Human_miRNA_ID_1908417 37735 RMVar_ID_37735 Human_SNP_ID_601430520 A-to-I Human chr16 - 46596255 46596255 46596255 GTGTTCTGCCCCCCTCGGCCTCCCAAAGTGCTAGGATTACAGGTGTGAGCTACCGCATGCGGCCT GTGTTCTGCCCCCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCTACCGCATGCGGCCT T C SHCBP1 Ensembl:ENSG00000171241 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1292820303 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88436,RMVar_hsa_circ_339058,RMVar_hsa_circ_178077 37736 RMVar_ID_37736 Human_SNP_ID_601430995 A-to-I Human chr16 - 46598411 46598411 46598411 TTATTGACAATGTACCTGGTCATCTGAGAGCTATGATGGAGGTGTACTGGGAGATTAATGTTGTT TTATTGACAATGTACCTGGTCATCTGAGAGCTGTGATGGAGGTGTACTGGGAGATTAATGTTGTT T C SHCBP1 Ensembl:ENSG00000171241 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs8050258 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88436,RMVar_hsa_circ_339058,RMVar_hsa_circ_178077 37737 RMVar_ID_37737 Human_SNP_ID_601431521 A-to-I Human chr16 - 46600416 46600416 46600416 CAGAATGAAGGCTGGAGTGCAATGGCATGATCATAGCTTACTGCAGCCTTAAAATTCTGGGATCA CAGAATGAAGGCTGGAGTGCAATGGCATGATCGTAGCTTACTGCAGCCTTAAAATTCTGGGATCA T C SHCBP1 Ensembl:ENSG00000171241 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs755228913 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88436,RMVar_hsa_circ_57712,RMVar_hsa_circ_178077,RMVar_hsa_circ_265079,RMVar_hsa_circ_362364,RMVar_hsa_circ_25355 37738 RMVar_ID_37738 Human_SNP_ID_601446054 A-to-I Human chr16 - 46660944 46660944 46660944 TGGGGTTCCACCATGTTGGCCAGGCTGGTCTCAAAACTCCTGACTTCAAGTGATCTGCCCACCTC TGGGGTTCCACCATGTTGGCCAGGCTGGTCTCGAAACTCCTGACTTCAAGTGATCTGCCCACCTC T C VPS35,AC012186.2 Ensembl:ENSG00000069329,Ensembl:ENSG00000261131 Protein coding,lincRNA intron,exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs910906954 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109612,RMVar_hsa_circ_119854,RMVar_hsa_circ_178084,RMVar_hsa_circ_94967,RMVar_hsa_circ_99770,RMVar_hsa_circ_89126,RMVar_hsa_circ_178085,RMVar_hsa_circ_178082,RMVar_hsa_circ_178083,RMVar_hsa_circ_178081 37739 RMVar_ID_37739 Human_SNP_ID_601455363 A-to-I Human chr16 + 46697994 46697994 46697994 AAAATTAGCCAGGTGTGATGGTGCATGCCTGTAATCCCAGCTCCTCAGTAGGCTGAGACAGGAGC AAAATTAGCCAGGTGTGATGGTGCATGCCTGTGATCCCAGCTCCTCAGTAGGCTGAGACAGGAGC A G ORC6 Ensembl:ENSG00000091651 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992039847 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_474396,Human_RBP_ID_23689649,Human_RBP_ID_26441347 RMVar_hsa_circ_117790,RMVar_hsa_circ_178107 37740 RMVar_ID_37740 Human_SNP_ID_601455380 A-to-I Human chr16 + 46698047 46698041 46698047 TGAGACAGGAGCATCACTTGAACGTGGGAGGCAGAGGTTGCAGTGAGCCGAGATTGCACCACCGC TGAGACAGGAGCATCACTTGAACGTGG______GAGGTTGCAGTGAGCCGAGATTGCACCACCGC GGAGGCA G ORC6 Ensembl:ENSG00000091651 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1224532884 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_474396,Human_RBP_ID_9062304,Human_RBP_ID_12739402,Human_RBP_ID_22582477,Human_RBP_ID_23689649,Human_RBP_ID_25210641 RMVar_hsa_circ_117790,RMVar_hsa_circ_178107 37741 RMVar_ID_37741 Human_SNP_ID_601456980 A-to-I Human chr16 - 46704538 46704538 46704538 GGGAGGCTGAGGCCAGAGAATCACTTGAACCCAGGGGGTGGAGGTTGCAGTGAGCCAAGATCACA GGGAGGCTGAGGCCAGAGAATCACTTGAACCCTGGGGGTGGAGGTTGCAGTGAGCCAAGATCACA T A MYLK3 Ensembl:ENSG00000140795 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968052941 Functional Loss SNV dbSNP153 33..33 33 - - - 37742 RMVar_ID_37742 Human_SNP_ID_601456981 A-to-I Human chr16 - 46704538 46704538 46704538 GGGAGGCTGAGGCCAGAGAATCACTTGAACCCAGGGGGTGGAGGTTGCAGTGAGCCAAGATCACA GGGAGGCTGAGGCCAGAGAATCACTTGAACCCGGGGGGTGGAGGTTGCAGTGAGCCAAGATCACA T C MYLK3 Ensembl:ENSG00000140795 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968052941 Functional Loss SNV dbSNP153 33..33 33 - - - 37743 RMVar_ID_37743 Human_SNP_ID_601457118 A-to-I Human chr16 - 46705304 46705304 46705304 GCTGGTCTCGAACTCCTGACCTCAGATGATCCACCTGTCTTGGCCTCCCAAAGAGCTGGGAATAT GCTGGTCTCGAACTCCTGACCTCAGATGATCCCCCTGTCTTGGCCTCCCAAAGAGCTGGGAATAT T G MYLK3 Ensembl:ENSG00000140795 Protein coding 3'UTR GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs1057051869 Functional Loss SNV dbSNP153 33..33 33 - - - 37744 RMVar_ID_37744 Human_SNP_ID_601457143 A-to-I Human chr16 - 46705406 46705406 46705406 TGTGCCTCAGCCTCCCAGGTAGCTGGGATTACAGGCGTGTGCTGCCACGCCCAGCTAATTTTTGT TGTGCCTCAGCCTCCCAGGTAGCTGGGATTACGGGCGTGTGCTGCCACGCCCAGCTAATTTTTGT T C MYLK3 Ensembl:ENSG00000140795 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1281838789 Functional Loss SNV dbSNP153 33..33 33 - - - 37745 RMVar_ID_37745 Human_SNP_ID_601457224 A-to-I Human chr16 - 46705778 46705778 46705778 TTTGCCATGTTGCCCAACCTGGTCTTGAGCTCAAGCGATCCACCTGCCCCAGCCTCCCAAAGTGC TTTGCCATGTTGCCCAACCTGGTCTTGAGCTCCAGCGATCCACCTGCCCCAGCCTCCCAAAGTGC T G MYLK3 Ensembl:ENSG00000140795 Protein coding 3'UTR GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs1205626078 Functional Loss SNV dbSNP153 33..33 33 - - - 37746 RMVar_ID_37746 Human_SNP_ID_601457249 A-to-I Human chr16 - 46705863 46705863 46705863 GGGCTCAGGCGATCATGAGTACCTGGGACCATAGGTGCCCGCTACTACACCCAGCTAATTTTTGT GGGCTCAGGCGATCATGAGTACCTGGGACCATGGGTGCCCGCTACTACACCCAGCTAATTTTTGT T C MYLK3 Ensembl:ENSG00000140795 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1051245371 Functional Loss SNV dbSNP153 33..33 33 - - - 37747 RMVar_ID_37747 Human_SNP_ID_601457399 A-to-I Human chr16 - 46706361 46706361 46706361 TGAACCTGGGAGGTGGAGTTTGCAGTGAGCCAAGATTGCACCACTGCACTCCAGCCTAGGCAACA TGAACCTGGGAGGTGGAGTTTGCAGTGAGCCACGATTGCACCACTGCACTCCAGCCTAGGCAACA T G MYLK3 Ensembl:ENSG00000140795 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs573659589 Functional Loss SNV dbSNP153 33..33 33 - - - 37748 RMVar_ID_37748 Human_SNP_ID_601457405 A-to-I Human chr16 - 46706431 46706431 46706431 AAATTAGTGGGGCGTGGTGGCGGATGCCTGTAATGTCAGCTACTCTGGAGGCTGAGGCAGGAGAA AAATTAGTGGGGCGTGGTGGCGGATGCCTGTAGTGTCAGCTACTCTGGAGGCTGAGGCAGGAGAA T C MYLK3 Ensembl:ENSG00000140795 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1412193057 Functional Loss SNV dbSNP153 33..33 33 - - - 37749 RMVar_ID_37749 Human_SNP_ID_601457406 A-to-I Human chr16 - 46706432 46706432 46706432 AAAATTAGTGGGGCGTGGTGGCGGATGCCTGTAATGTCAGCTACTCTGGAGGCTGAGGCAGGAGA AAAATTAGTGGGGCGTGGTGGCGGATGCCTGTGATGTCAGCTACTCTGGAGGCTGAGGCAGGAGA T C MYLK3 Ensembl:ENSG00000140795 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909771875 Functional Loss SNV dbSNP153 33..33 33 - - - 37750 RMVar_ID_37750 Human_SNP_ID_601457430 A-to-I Human chr16 - 46706566 46706566 46706566 ATATAAGCTGGGTGTGGTGGCTCATGCCCATAATCCCAGCACTTTGGGAGGCTGAGGCAGGCAGA ATATAAGCTGGGTGTGGTGGCTCATGCCCATAGTCCCAGCACTTTGGGAGGCTGAGGCAGGCAGA T C MYLK3 Ensembl:ENSG00000140795 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1330902718 Functional Loss SNV dbSNP153 33..33 33 - - - 37751 RMVar_ID_37751 Human_SNP_ID_601457431 A-to-I Human chr16 - 46706569 46706569 46706569 AGTATATAAGCTGGGTGTGGTGGCTCATGCCCATAATCCCAGCACTTTGGGAGGCTGAGGCAGGC AGTATATAAGCTGGGTGTGGTGGCTCATGCCCGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGC T C MYLK3 Ensembl:ENSG00000140795 Protein coding 3'UTR GSE100210;GSE99789 HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 29129909,29796672 RNA-Seq:(High) rs1333943016 Functional Loss SNV dbSNP153 33..33 33 - - - 37752 RMVar_ID_37752 Human_SNP_ID_601460501 A-to-I Human chr16 - 46719699 46719699 46719699 GCAGGGGTGGTGACAGATGCATCGCATAGCCCAGCATGTCCTAGCCCCAGGAGGCCTGCGGAACC GCAGGGGTGGTGACAGATGCATCGCATAGCCCGGCATGTCCTAGCCCCAGGAGGCCTGCGGAACC T C MYLK3 Ensembl:ENSG00000140795 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1180936868 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7725,RMVar_hsa_circ_321139,RMVar_hsa_circ_35028 37753 RMVar_ID_37753 Human_SNP_ID_601479436 A-to-I Human chr16 - 46797620 46797620 46797620 TAAGACTTGGCTGGGCACAGTGGCTCACCTGTAATCCCAGGACTGGGAGGCCGAGGCGAGCAGAT TAAGACTTGGCTGGGCACAGTGGCTCACCTGTCATCCCAGGACTGGGAGGCCGAGGCGAGCAGAT T G C16orf87 Ensembl:ENSG00000155330 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1567302294 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6513992,Human_RBP_ID_12739836 37754 RMVar_ID_37754 Human_SNP_ID_601479589 A-to-I Human chr16 - 46798425 46798425 46798425 TGCAACCTTGCAACCTCTGCCTCCCGAGTTCAAGCGATTCTCCTGCCTTAGCCTCCTGAGTAGCT TGCAACCTTGCAACCTCTGCCTCCCGAGTTCAGGCGATTCTCCTGCCTTAGCCTCCTGAGTAGCT T C C16orf87 Ensembl:ENSG00000155330 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1160195710 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12739858 37755 RMVar_ID_37755 Human_SNP_ID_601479849 A-to-I Human chr16 - 46799758 46799758 46799758 TCCAGCTACTAGGCAGCTGAGGCTAAAGGATCACTTGAGCCCAGGAGTTCGAGGCTGCAGTGAGT TCCAGCTACTAGGCAGCTGAGGCTAAAGGATCCCTTGAGCCCAGGAGTTCGAGGCTGCAGTGAGT T G C16orf87 Ensembl:ENSG00000155330 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs886805026 Functional Loss SNV dbSNP153 33..33 33 - - - 37756 RMVar_ID_37756 Human_SNP_ID_601480210 A-to-I Human chr16 - 46801463 46801463 46801463 CAGGCTGGAGTGCAGTGGCACTGTCTCAGCTCACTGCAACCTCTGCCTCCTGGGTTCAAGTGATT CAGGCTGGAGTGCAGTGGCACTGTCTCAGCTCGCTGCAACCTCTGCCTCCTGGGTTCAAGTGATT T C C16orf87 Ensembl:ENSG00000155330 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1236340989 Functional Loss SNV dbSNP153 33..33 33 - - - 37757 RMVar_ID_37757 Human_SNP_ID_601480226 A-to-I Human chr16 - 46801521 46801521 46801521 AACTATTTTGTATGCATTTTATTTATTTATTTAGGAGACAGAGTCTTGCTCGGTCGCCCAGGCTG AACTATTTTGTATGCATTTTATTTATTTATTTGGGAGACAGAGTCTTGCTCGGTCGCCCAGGCTG T C C16orf87 Ensembl:ENSG00000155330 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1336455594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_474458,Human_RBP_ID_6514084,Human_RBP_ID_17877091,Human_RBP_ID_20120523 37758 RMVar_ID_37758 Human_SNP_ID_601506022 A-to-I Human chr16 + 46910735 46910735 46910735 TTCCTGTCTCAGCCTCCTGAGTAGCTCAGACTACAGGCAGCACCACCACGCCCAGCTAATATTTT TTCCTGTCTCAGCCTCCTGAGTAGCTCAGACTCCAGGCAGCACCACCACGCCCAGCTAATATTTT A C GPT2 Ensembl:ENSG00000166123 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1297924661 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8486,RMVar_hsa_circ_349131,RMVar_hsa_circ_178113,RMVar_hsa_circ_373404,RMVar_hsa_circ_127742,RMVar_hsa_circ_178114,RMVar_hsa_circ_332278,RMVar_hsa_circ_323194,RMVar_hsa_circ_349349,RMVar_hsa_circ_91120,RMVar_hsa_circ_46868,RMVar_hsa_circ_178117,RMVar_hsa_circ_178118,RMVar_hsa_circ_178116,RMVar_hsa_circ_85191,RMVar_hsa_circ_178120 37759 RMVar_ID_37759 Human_SNP_ID_601506964 A-to-I Human chr16 + 46915145 46915145 46915145 TGTTGCCCATGCGGTCTGGAACTCCTGGGCTCAAGCGGTCCTCCCACCCTGGCCTCCCGAAGCCG TGTTGCCCATGCGGTCTGGAACTCCTGGGCTCCAGCGGTCCTCCCACCCTGGCCTCCCGAAGCCG A C GPT2 Ensembl:ENSG00000166123 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs901131474 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_197978,Human_RBP_ID_9419828,Human_RBP_ID_26757296 RMVar_hsa_circ_8486,RMVar_hsa_circ_349131,RMVar_hsa_circ_178113,RMVar_hsa_circ_373404,RMVar_hsa_circ_127742,RMVar_hsa_circ_178114,RMVar_hsa_circ_332278,RMVar_hsa_circ_323194,RMVar_hsa_circ_349349,RMVar_hsa_circ_91120,RMVar_hsa_circ_46868,RMVar_hsa_circ_178117,RMVar_hsa_circ_178118,RMVar_hsa_circ_178116,RMVar_hsa_circ_85191,RMVar_hsa_circ_178120 37760 RMVar_ID_37760 Human_SNP_ID_601506965 A-to-I Human chr16 + 46915145 46915145 46915145 TGTTGCCCATGCGGTCTGGAACTCCTGGGCTCAAGCGGTCCTCCCACCCTGGCCTCCCGAAGCCG TGTTGCCCATGCGGTCTGGAACTCCTGGGCTCGAGCGGTCCTCCCACCCTGGCCTCCCGAAGCCG A G GPT2 Ensembl:ENSG00000166123 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs901131474 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_197978,Human_RBP_ID_9419828,Human_RBP_ID_26757296 RMVar_hsa_circ_8486,RMVar_hsa_circ_349131,RMVar_hsa_circ_178113,RMVar_hsa_circ_373404,RMVar_hsa_circ_127742,RMVar_hsa_circ_178114,RMVar_hsa_circ_332278,RMVar_hsa_circ_323194,RMVar_hsa_circ_349349,RMVar_hsa_circ_91120,RMVar_hsa_circ_46868,RMVar_hsa_circ_178117,RMVar_hsa_circ_178118,RMVar_hsa_circ_178116,RMVar_hsa_circ_85191,RMVar_hsa_circ_178120 37761 RMVar_ID_37761 Human_SNP_ID_601509432 A-to-I Human chr16 + 46924264 46924263 46924265 AAATCTGAGTCAACGCATGGGTCAGAGGGGACATGTGTTCAAAGCTGGAGCAAAGTCATCATCTG AAATCTGAGTCAACGCATGGGTCAGAGGGGAC__GTGTTCAAAGCTGGAGCAAAGTCATCATCTG CAT C GPT2 Ensembl:ENSG00000166123 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs771321276 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_5360316 RMVar_hsa_circ_127742,RMVar_hsa_circ_91120,RMVar_hsa_circ_46868,RMVar_hsa_circ_178117,RMVar_hsa_circ_178118,RMVar_hsa_circ_115777,RMVar_hsa_circ_343140,RMVar_hsa_circ_178121,RMVar_hsa_circ_178122 37762 RMVar_ID_37762 Human_SNP_ID_601509434 A-to-I Human chr16 + 46924264 46924264 46924264 AAATCTGAGTCAACGCATGGGTCAGAGGGGACATGTGTTCAAAGCTGGAGCAAAGTCATCATCTG AAATCTGAGTCAACGCATGGGTCAGAGGGGACGTGTGTTCAAAGCTGGAGCAAAGTCATCATCTG A G GPT2 Ensembl:ENSG00000166123 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs779004477 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5360316 RMVar_hsa_circ_127742,RMVar_hsa_circ_91120,RMVar_hsa_circ_46868,RMVar_hsa_circ_178117,RMVar_hsa_circ_178118,RMVar_hsa_circ_115777,RMVar_hsa_circ_343140,RMVar_hsa_circ_178121,RMVar_hsa_circ_178122 37763 RMVar_ID_37763 Human_SNP_ID_601517574 A-to-I Human chr16 - 46957088 46957088 46957088 GAGGTGGTCAGAGGCGTGAAGCCTATAATGATAGCTCTGATGAAGAAAGCAGCAGCCATCATGGA GAGGTGGTCAGAGGCGTGAAGCCTATAATGATGGCTCTGATGAAGAAAGCAGCAGCCATCATGGA T C DNAJA2 Ensembl:ENSG00000069345 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs765773216 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_43709,Human_RBP_ID_1842751,Human_RBP_ID_6514504,Human_RBP_ID_8434151,Human_RBP_ID_17653433,Human_RBP_ID_17884114,Human_RBP_ID_27242383 RMVar_hsa_circ_84462,RMVar_hsa_circ_120220,RMVar_hsa_circ_178127,RMVar_hsa_circ_178128 37764 RMVar_ID_37764 Human_SNP_ID_601554843 A-to-I Human chr16 - 47109519 47109519 47109519 TTCGAATGTGGGCAGATGAAGGTAGTCGGCTTAGCAGGTTTCGAATGCTCTTTACTTCCTTTGTG TTCGAATGTGGGCAGATGAAGGTAGTCGGCTTGGCAGGTTTCGAATGCTCTTTACTTCCTTTGTG T C NETO2 Ensembl:ENSG00000171208 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1244154845 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6514760,Human_RBP_ID_8807998 Human_Splice_Rec_1708395,Human_Splice_Rec_1708411,Human_Splice_Rec_1708421,Human_Splice_Rec_1708429 Human_miRNA_ID_1953767 RMVar_hsa_circ_14041,RMVar_hsa_circ_267580,RMVar_hsa_circ_308524,RMVar_hsa_circ_371315,RMVar_hsa_circ_178136,RMVar_hsa_circ_178133,RMVar_hsa_circ_178134,RMVar_hsa_circ_178138,RMVar_hsa_circ_273784,RMVar_hsa_circ_274486,RMVar_hsa_circ_109873,RMVar_hsa_circ_178137,RMVar_hsa_circ_178135 37765 RMVar_ID_37765 Human_SNP_ID_601566218 A-to-I Human chr16 - 47156330 47156330 47156330 GGTTCAAGCGATTCTCCTGCCTTAGCCTCCCAAGAAGCTGTGATTACAGGTGCCCACCACCACAC GGTTCAAGCGATTCTCCTGCCTTAGCCTCCCACGAAGCTGTGATTACAGGTGCCCACCACCACAC T G ITFG1 Ensembl:ENSG00000129636 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs758343017 Functional Loss SNV dbSNP153 33..33 33 - - - 37766 RMVar_ID_37766 Human_SNP_ID_601566220 A-to-I Human chr16 - 47156339 47156339 47156339 CCGCTCCTGGGTTCAAGCGATTCTCCTGCCTTAGCCTCCCAAGAAGCTGTGATTACAGGTGCCCA CCGCTCCTGGGTTCAAGCGATTCTCCTGCCTTGGCCTCCCAAGAAGCTGTGATTACAGGTGCCCA T C ITFG1 Ensembl:ENSG00000129636 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs764193082 Functional Loss SNV dbSNP153 33..33 33 - - - 37767 RMVar_ID_37767 Human_SNP_ID_601566578 A-to-I Human chr16 - 47158219 47158219 47158219 ACCATGATGCAAGCCTGTAATCTCAGCTACTCAGGAGGCTGAGGTCGGAGAATCACCTGAGCCCA ACCATGATGCAAGCCTGTAATCTCAGCTACTCGGGAGGCTGAGGTCGGAGAATCACCTGAGCCCA T C ITFG1 Ensembl:ENSG00000129636 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs969633970 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27442973 37768 RMVar_ID_37768 Human_SNP_ID_601579978 A-to-I Human chr16 - 47216232 47216232 47216232 TGAGGGCATTGCACTCCAGCTAGGTGACAAGAACAAAACTCCGTCTCAGAAAAAAAAAAAATGGG TGAGGGCATTGCACTCCAGCTAGGTGACAAGACCAAAACTCCGTCTCAGAAAAAAAAAAAATGGG T G ITFG1 Ensembl:ENSG00000129636 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474262609 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2475457 37769 RMVar_ID_37769 Human_SNP_ID_601580005 A-to-I Human chr16 - 47216332 47216332 47216332 GAAATTAGCCAGGTGTGGTGGCACATGCCTGTAGTCCCAGCTACTTCGGGAGGCTGGGGCAGGAG GAAATTAGCCAGGTGTGGTGGCACATGCCTGTTGTCCCAGCTACTTCGGGAGGCTGGGGCAGGAG T A ITFG1 Ensembl:ENSG00000129636 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1460014812 Functional Loss SNV dbSNP153 33..33 33 - - - 37770 RMVar_ID_37770 Human_SNP_ID_601580352 A-to-I Human chr16 - 47217813 47217813 47217813 TCCCGCCATTCTCCTGCCTCAGCCTCCCGAGCAGCTGGGACCACAGGTGCCCGCCACTACACCCG TCCCGCCATTCTCCTGCCTCAGCCTCCCGAGCCGCTGGGACCACAGGTGCCCGCCACTACACCCG T G ITFG1 Ensembl:ENSG00000129636 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1463686829 Functional Loss SNV dbSNP153 33..33 33 - - - 37771 RMVar_ID_37771 Human_SNP_ID_601595647 A-to-I Human chr16 - 47287622 47287622 47287622 GAGGTGAGGGAATTGCTTGAGCCCAGGAGTTCAAGACCAGCCTGGATAACATAGTGAGGCCCTGT GAGGTGAGGGAATTGCTTGAGCCCAGGAGTTCGAGACCAGCCTGGATAACATAGTGAGGCCCTGT T C ITFG1 Ensembl:ENSG00000129636 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1325311470 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1493,RMVar_hsa_circ_336738,RMVar_hsa_circ_375933,RMVar_hsa_circ_279142,RMVar_hsa_circ_19565,RMVar_hsa_circ_178143,RMVar_hsa_circ_178145,RMVar_hsa_circ_178144,RMVar_hsa_circ_313722,RMVar_hsa_circ_22738,RMVar_hsa_circ_270482,RMVar_hsa_circ_178148,RMVar_hsa_circ_99725,RMVar_hsa_circ_20157,RMVar_hsa_circ_178149,RMVar_hsa_circ_178150,RMVar_hsa_circ_178151 37772 RMVar_ID_37772 Human_SNP_ID_601595868 A-to-I Human chr16 - 47288776 47288776 47288776 TTCTCGTGCCTCAGCCCCAAGTAGCTGGGACTACAGGTGTGCACCACCACGCTGGCTAGTTTTTG TTCTCGTGCCTCAGCCCCAAGTAGCTGGGACTGCAGGTGTGCACCACCACGCTGGCTAGTTTTTG T C ITFG1 Ensembl:ENSG00000129636 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1567446850 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1493,RMVar_hsa_circ_336738,RMVar_hsa_circ_375933,RMVar_hsa_circ_279142,RMVar_hsa_circ_19565,RMVar_hsa_circ_178143,RMVar_hsa_circ_178145,RMVar_hsa_circ_178144,RMVar_hsa_circ_313722,RMVar_hsa_circ_22738,RMVar_hsa_circ_270482,RMVar_hsa_circ_178148,RMVar_hsa_circ_99725,RMVar_hsa_circ_20157,RMVar_hsa_circ_178149,RMVar_hsa_circ_178150,RMVar_hsa_circ_178151 37773 RMVar_ID_37773 Human_SNP_ID_601595879 A-to-I Human chr16 - 47288833 47288833 47288833 GGAGTGCAGTGGTGCAATCTCGACTCGCTGCAACCTCCACTTCTTGGGTTCAAGCGATTCTCGTG GGAGTGCAGTGGTGCAATCTCGACTCGCTGCACCCTCCACTTCTTGGGTTCAAGCGATTCTCGTG T G ITFG1 Ensembl:ENSG00000129636 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1345917858 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1493,RMVar_hsa_circ_336738,RMVar_hsa_circ_375933,RMVar_hsa_circ_279142,RMVar_hsa_circ_19565,RMVar_hsa_circ_178143,RMVar_hsa_circ_178145,RMVar_hsa_circ_178144,RMVar_hsa_circ_313722,RMVar_hsa_circ_22738,RMVar_hsa_circ_270482,RMVar_hsa_circ_178148,RMVar_hsa_circ_99725,RMVar_hsa_circ_20157,RMVar_hsa_circ_178149,RMVar_hsa_circ_178150,RMVar_hsa_circ_178151 37774 RMVar_ID_37774 Human_SNP_ID_601607902 A-to-I Human chr16 - 47339140 47339140 47339140 CTATATAACTGAGTACTATTCAGGCATAAGAAAGAATGAGATTACATCATTTGCAACAACATGGA CTATATAACTGAGTACTATTCAGGCATAAGAATGAATGAGATTACATCATTTGCAACAACATGGA T A ITFG1 Ensembl:ENSG00000129636 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1210461649 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1493,RMVar_hsa_circ_336738,RMVar_hsa_circ_375933,RMVar_hsa_circ_19565,RMVar_hsa_circ_178143,RMVar_hsa_circ_22738,RMVar_hsa_circ_99725,RMVar_hsa_circ_20157,RMVar_hsa_circ_75478,RMVar_hsa_circ_29857,RMVar_hsa_circ_321262,RMVar_hsa_circ_178151,RMVar_hsa_circ_329046,RMVar_hsa_circ_372039,RMVar_hsa_circ_283200,RMVar_hsa_circ_41904,RMVar_hsa_circ_178155,RMVar_hsa_circ_20126,RMVar_hsa_circ_178156,RMVar_hsa_circ_178154 37775 RMVar_ID_37775 Human_SNP_ID_601629237 A-to-I Human chr16 - 47427942 47427942 47427942 TTTTGTAGAGACAGAGTTTCCCTATGTTGCCTAGACTGGTCTTGAACTCCTTGGCTCAAGCAATC TTTTGTAGAGACAGAGTTTCCCTATGTTGCCTGGACTGGTCTTGAACTCCTTGGCTCAAGCAATC T C ITFG1 Ensembl:ENSG00000129636 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs773585031 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25211539 RMVar_hsa_circ_375933,RMVar_hsa_circ_19565,RMVar_hsa_circ_178143,RMVar_hsa_circ_22738,RMVar_hsa_circ_29857,RMVar_hsa_circ_321262,RMVar_hsa_circ_372039,RMVar_hsa_circ_283200,RMVar_hsa_circ_178155,RMVar_hsa_circ_20126,RMVar_hsa_circ_178156,RMVar_hsa_circ_178154,RMVar_hsa_circ_275027,RMVar_hsa_circ_361517,RMVar_hsa_circ_80837,RMVar_hsa_circ_178157,RMVar_hsa_circ_178158 37776 RMVar_ID_37776 Human_SNP_ID_601629251 A-to-I Human chr16 - 47428006 47428006 47428006 CCTCAGCCTCGAGAGCATCTAGGACTACAAGCATGTGCCATTATGCCTGGCTAATTCTTGTATTT CCTCAGCCTCGAGAGCATCTAGGACTACAAGCGTGTGCCATTATGCCTGGCTAATTCTTGTATTT T C ITFG1 Ensembl:ENSG00000129636 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1191753852 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_375933,RMVar_hsa_circ_19565,RMVar_hsa_circ_178143,RMVar_hsa_circ_22738,RMVar_hsa_circ_29857,RMVar_hsa_circ_321262,RMVar_hsa_circ_372039,RMVar_hsa_circ_283200,RMVar_hsa_circ_178155,RMVar_hsa_circ_20126,RMVar_hsa_circ_178156,RMVar_hsa_circ_178154,RMVar_hsa_circ_275027,RMVar_hsa_circ_361517,RMVar_hsa_circ_80837,RMVar_hsa_circ_178157,RMVar_hsa_circ_178158 37777 RMVar_ID_37777 Human_SNP_ID_601629567 A-to-I Human chr16 - 47429302 47429302 47429302 TAAACCCATACAATGGAATATTATTCCGCTATAGAAAGAACTGAGGCACTGATACATGTTTCAAC TAAACCCATACAATGGAATATTATTCCGCTATGGAAAGAACTGAGGCACTGATACATGTTTCAAC T C ITFG1 Ensembl:ENSG00000129636 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1567497389 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_375933,RMVar_hsa_circ_178143,RMVar_hsa_circ_29857,RMVar_hsa_circ_321262,RMVar_hsa_circ_372039,RMVar_hsa_circ_178155,RMVar_hsa_circ_20126,RMVar_hsa_circ_178156,RMVar_hsa_circ_12731,RMVar_hsa_circ_361517,RMVar_hsa_circ_80837,RMVar_hsa_circ_178157,RMVar_hsa_circ_274176,RMVar_hsa_circ_178159 37778 RMVar_ID_37778 Human_SNP_ID_601667313 A-to-I Human chr16 + 47590310 47590310 47590310 TTAACTTTTTTTTTTTTTTTTTAATAGAGACCAGATCTCCCTATGTTGCCCAGGCTGGACTGGAA TTAACTTTTTTTTTTTTTTTTTAATAGAGACCGGATCTCCCTATGTTGCCCAGGCTGGACTGGAA A G PHKB Ensembl:ENSG00000102893 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs527568103 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1708852 RMVar_hsa_circ_83247,RMVar_hsa_circ_178164,RMVar_hsa_circ_127228,RMVar_hsa_circ_334402,RMVar_hsa_circ_178161,RMVar_hsa_circ_121637,RMVar_hsa_circ_292809,RMVar_hsa_circ_318878,RMVar_hsa_circ_290052,RMVar_hsa_circ_44937,RMVar_hsa_circ_106295,RMVar_hsa_circ_123850,RMVar_hsa_circ_84072,RMVar_hsa_circ_37992,RMVar_hsa_circ_178166,RMVar_hsa_circ_7337,RMVar_hsa_circ_178167,RMVar_hsa_circ_178165,RMVar_hsa_circ_305356,RMVar_hsa_circ_315502,RMVar_hsa_circ_325832,RMVar_hsa_circ_275768,RMVar_hsa_circ_282688,RMVar_hsa_circ_273795,RMVar_hsa_circ_118486,RMVar_hsa_circ_43430,RMVar_hsa_circ_17281,RMVar_hsa_circ_178173,RMVar_hsa_circ_178175,RMVar_hsa_circ_178174,RMVar_hsa_circ_178171,RMVar_hsa_circ_178172,RMVar_hsa_circ_106120,RMVar_hsa_circ_178186,RMVar_hsa_circ_81615,RMVar_hsa_circ_178188,RMVar_hsa_circ_178190,RMVar_hsa_circ_112840,RMVar_hsa_circ_374198,RMVar_hsa_circ_46572,RMVar_hsa_circ_178189,RMVar_hsa_circ_319621,RMVar_hsa_circ_46538,RMVar_hsa_circ_127374,RMVar_hsa_circ_110646,RMVar_hsa_circ_178192,RMVar_hsa_circ_178195,RMVar_hsa_circ_281064,RMVar_hsa_circ_178196,RMVar_hsa_circ_18107,RMVar_hsa_circ_61597,RMVar_hsa_circ_178197,RMVar_hsa_circ_113818,RMVar_hsa_circ_313469,RMVar_hsa_circ_178198,RMVar_hsa_circ_313809,RMVar_hsa_circ_35807,RMVar_hsa_circ_178199 37779 RMVar_ID_37779 Human_SNP_ID_601837511 A-to-I Human chr16 + 48296588 48296588 48296588 CATCTCAATAAAAATACAAAAATTAGCCTGGCATGGTGGCGGGCGCCTGTAGTCCCACCTACTCG CATCTCAATAAAAATACAAAAATTAGCCTGGCGTGGTGGCGGGCGCCTGTAGTCCCACCTACTCG A G LONP2 Ensembl:ENSG00000102910 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1033336090 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19268,RMVar_hsa_circ_178219,RMVar_hsa_circ_82057,RMVar_hsa_circ_106582,RMVar_hsa_circ_178220,RMVar_hsa_circ_283029,RMVar_hsa_circ_28218,RMVar_hsa_circ_178226,RMVar_hsa_circ_178221,RMVar_hsa_circ_274796,RMVar_hsa_circ_178228,RMVar_hsa_circ_178229,RMVar_hsa_circ_178231,RMVar_hsa_circ_330661,RMVar_hsa_circ_57064,RMVar_hsa_circ_178235,RMVar_hsa_circ_126671,RMVar_hsa_circ_178232,RMVar_hsa_circ_93110,RMVar_hsa_circ_31201,RMVar_hsa_circ_178236,RMVar_hsa_circ_75032,RMVar_hsa_circ_178237,RMVar_hsa_circ_124609,RMVar_hsa_circ_305911,RMVar_hsa_circ_178239,RMVar_hsa_circ_303926,RMVar_hsa_circ_342876,RMVar_hsa_circ_282849,RMVar_hsa_circ_77001,RMVar_hsa_circ_178240,RMVar_hsa_circ_178241,RMVar_hsa_circ_334449,RMVar_hsa_circ_357158,RMVar_hsa_circ_178243,RMVar_hsa_circ_178244 37780 RMVar_ID_37780 Human_SNP_ID_601838224 A-to-I Human chr16 + 48299327 48299327 48299327 ATGGCACTGGCTGGGAGCAGTGACTCATGCCTATAATCTCAGCACTTTGGGAGGCTGAGGCTGGT ATGGCACTGGCTGGGAGCAGTGACTCATGCCTTTAATCTCAGCACTTTGGGAGGCTGAGGCTGGT A T LONP2 Ensembl:ENSG00000102910 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1438504970 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19268,RMVar_hsa_circ_178219,RMVar_hsa_circ_82057,RMVar_hsa_circ_106582,RMVar_hsa_circ_178220,RMVar_hsa_circ_283029,RMVar_hsa_circ_28218,RMVar_hsa_circ_178226,RMVar_hsa_circ_178221,RMVar_hsa_circ_274796,RMVar_hsa_circ_178228,RMVar_hsa_circ_178229,RMVar_hsa_circ_178231,RMVar_hsa_circ_330661,RMVar_hsa_circ_57064,RMVar_hsa_circ_178235,RMVar_hsa_circ_126671,RMVar_hsa_circ_178232,RMVar_hsa_circ_93110,RMVar_hsa_circ_31201,RMVar_hsa_circ_178236,RMVar_hsa_circ_75032,RMVar_hsa_circ_178237,RMVar_hsa_circ_124609,RMVar_hsa_circ_305911,RMVar_hsa_circ_178239,RMVar_hsa_circ_303926,RMVar_hsa_circ_342876,RMVar_hsa_circ_282849,RMVar_hsa_circ_77001,RMVar_hsa_circ_178240,RMVar_hsa_circ_178241,RMVar_hsa_circ_334449,RMVar_hsa_circ_357158,RMVar_hsa_circ_178243,RMVar_hsa_circ_178244 37781 RMVar_ID_37781 Human_SNP_ID_601838226 A-to-I Human chr16 + 48299338 48299338 48299338 TGGGAGCAGTGACTCATGCCTATAATCTCAGCACTTTGGGAGGCTGAGGCTGGTGGATCACTTGA TGGGAGCAGTGACTCATGCCTATAATCTCAGCCCTTTGGGAGGCTGAGGCTGGTGGATCACTTGA A C LONP2 Ensembl:ENSG00000102910 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs566532848 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19268,RMVar_hsa_circ_178219,RMVar_hsa_circ_82057,RMVar_hsa_circ_106582,RMVar_hsa_circ_178220,RMVar_hsa_circ_283029,RMVar_hsa_circ_28218,RMVar_hsa_circ_178226,RMVar_hsa_circ_178221,RMVar_hsa_circ_274796,RMVar_hsa_circ_178228,RMVar_hsa_circ_178229,RMVar_hsa_circ_178231,RMVar_hsa_circ_330661,RMVar_hsa_circ_57064,RMVar_hsa_circ_178235,RMVar_hsa_circ_126671,RMVar_hsa_circ_178232,RMVar_hsa_circ_93110,RMVar_hsa_circ_31201,RMVar_hsa_circ_178236,RMVar_hsa_circ_75032,RMVar_hsa_circ_178237,RMVar_hsa_circ_124609,RMVar_hsa_circ_305911,RMVar_hsa_circ_178239,RMVar_hsa_circ_303926,RMVar_hsa_circ_342876,RMVar_hsa_circ_282849,RMVar_hsa_circ_77001,RMVar_hsa_circ_178240,RMVar_hsa_circ_178241,RMVar_hsa_circ_334449,RMVar_hsa_circ_357158,RMVar_hsa_circ_178243,RMVar_hsa_circ_178244 37782 RMVar_ID_37782 Human_SNP_ID_601838227 A-to-I Human chr16 + 48299338 48299338 48299338 TGGGAGCAGTGACTCATGCCTATAATCTCAGCACTTTGGGAGGCTGAGGCTGGTGGATCACTTGA TGGGAGCAGTGACTCATGCCTATAATCTCAGCGCTTTGGGAGGCTGAGGCTGGTGGATCACTTGA A G LONP2 Ensembl:ENSG00000102910 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs566532848 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19268,RMVar_hsa_circ_178219,RMVar_hsa_circ_82057,RMVar_hsa_circ_106582,RMVar_hsa_circ_178220,RMVar_hsa_circ_283029,RMVar_hsa_circ_28218,RMVar_hsa_circ_178226,RMVar_hsa_circ_178221,RMVar_hsa_circ_274796,RMVar_hsa_circ_178228,RMVar_hsa_circ_178229,RMVar_hsa_circ_178231,RMVar_hsa_circ_330661,RMVar_hsa_circ_57064,RMVar_hsa_circ_178235,RMVar_hsa_circ_126671,RMVar_hsa_circ_178232,RMVar_hsa_circ_93110,RMVar_hsa_circ_31201,RMVar_hsa_circ_178236,RMVar_hsa_circ_75032,RMVar_hsa_circ_178237,RMVar_hsa_circ_124609,RMVar_hsa_circ_305911,RMVar_hsa_circ_178239,RMVar_hsa_circ_303926,RMVar_hsa_circ_342876,RMVar_hsa_circ_282849,RMVar_hsa_circ_77001,RMVar_hsa_circ_178240,RMVar_hsa_circ_178241,RMVar_hsa_circ_334449,RMVar_hsa_circ_357158,RMVar_hsa_circ_178243,RMVar_hsa_circ_178244 37783 RMVar_ID_37783 Human_SNP_ID_601840328 A-to-I Human chr16 + 48309067 48309066 48309067 AGGAAGCATTTGAAAAAATGCTCAATATCACTAATCATCAGAGAAATGAAAAATCTATGAGATAC AGGAAGCATTTGAAAAAATGCTCAATATCACT_ATCATCAGAGAAATGAAAAATCTATGAGATAC TA T LONP2 Ensembl:ENSG00000102910 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1406391175 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_19268,RMVar_hsa_circ_106582,RMVar_hsa_circ_178220,RMVar_hsa_circ_28218,RMVar_hsa_circ_178226,RMVar_hsa_circ_178229,RMVar_hsa_circ_57064,RMVar_hsa_circ_126671,RMVar_hsa_circ_178236,RMVar_hsa_circ_75032,RMVar_hsa_circ_303926,RMVar_hsa_circ_342876,RMVar_hsa_circ_77001,RMVar_hsa_circ_178241,RMVar_hsa_circ_357158,RMVar_hsa_circ_178244,RMVar_hsa_circ_375446,RMVar_hsa_circ_178245,RMVar_hsa_circ_101762,RMVar_hsa_circ_178248 37784 RMVar_ID_37784 Human_SNP_ID_601840398 A-to-I Human chr16 + 48309473 48309473 48309473 GTGACAATAACTCAGAAATTCAAATACTGAATATTCTCATTTATAAGTGGAAGCCAAATAATGTG GTGACAATAACTCAGAAATTCAAATACTGAATGTTCTCATTTATAAGTGGAAGCCAAATAATGTG A G LONP2 Ensembl:ENSG00000102910 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202790249 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18285761 RMVar_hsa_circ_19268,RMVar_hsa_circ_106582,RMVar_hsa_circ_178220,RMVar_hsa_circ_28218,RMVar_hsa_circ_178226,RMVar_hsa_circ_178229,RMVar_hsa_circ_57064,RMVar_hsa_circ_126671,RMVar_hsa_circ_178236,RMVar_hsa_circ_75032,RMVar_hsa_circ_303926,RMVar_hsa_circ_342876,RMVar_hsa_circ_77001,RMVar_hsa_circ_178241,RMVar_hsa_circ_357158,RMVar_hsa_circ_178244,RMVar_hsa_circ_375446,RMVar_hsa_circ_178245,RMVar_hsa_circ_101762,RMVar_hsa_circ_178248 37785 RMVar_ID_37785 Human_SNP_ID_601845413 A-to-I Human chr16 + 48332326 48332325 48332326 TGCTGGACGTGGTGGCTCACACCTGTAATCCCAACACTATGGGAAGCTGAGGCAGCCAGATCACT TGCTGGACGTGGTGGCTCACACCTGTAATCCC_ACACTATGGGAAGCTGAGGCAGCCAGATCACT CA C LONP2 Ensembl:ENSG00000102910 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1212929134 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_19268,RMVar_hsa_circ_106582,RMVar_hsa_circ_178220,RMVar_hsa_circ_28218,RMVar_hsa_circ_178226,RMVar_hsa_circ_178229,RMVar_hsa_circ_57064,RMVar_hsa_circ_126671,RMVar_hsa_circ_178236,RMVar_hsa_circ_75032,RMVar_hsa_circ_303926,RMVar_hsa_circ_342876,RMVar_hsa_circ_77001,RMVar_hsa_circ_178241,RMVar_hsa_circ_357158,RMVar_hsa_circ_178244,RMVar_hsa_circ_375446,RMVar_hsa_circ_178245,RMVar_hsa_circ_101762,RMVar_hsa_circ_178248 37786 RMVar_ID_37786 Human_SNP_ID_601849475 A-to-I Human chr16 + 48350241 48350241 48350241 AACCCTGTCTCTACTAAAAATACAAAAAAATTATCCGGATGTGGTGGCGCATGCCTGTAATCCCA AACCCTGTCTCTACTAAAAATACAAAAAAATTTTCCGGATGTGGTGGCGCATGCCTGTAATCCCA A T LONP2 Ensembl:ENSG00000102910 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1353963006 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77001,RMVar_hsa_circ_178244,RMVar_hsa_circ_79595,RMVar_hsa_circ_304721,RMVar_hsa_circ_178252 37787 RMVar_ID_37787 Human_SNP_ID_601850062 A-to-I Human chr16 + 48352384 48352384 48352384 TATATTCAAGTGGGCCGGGCGTGATGGCTCACACCTGTAATTCCAGCACTTTGGGAGGTCGAGGT TATATTCAAGTGGGCCGGGCGTGATGGCTCACGCCTGTAATTCCAGCACTTTGGGAGGTCGAGGT A G LONP2 Ensembl:ENSG00000102910 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs938678932 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17371752,Human_RBP_ID_26445134 Human_miRNA_ID_1738220,Human_miRNA_ID_1943185,Human_miRNA_ID_1946231,Human_miRNA_ID_2117376,Human_miRNA_ID_2200958,Human_miRNA_ID_2204021,Human_miRNA_ID_2316567,Human_miRNA_ID_2319723,Human_miRNA_ID_2322880,Human_miRNA_ID_2326052,Human_miRNA_ID_2520429,Human_miRNA_ID_2523591,Human_miRNA_ID_2775413,Human_miRNA_ID_2816480,Human_miRNA_ID_2822780,Human_miRNA_ID_2828915,Human_miRNA_ID_2832074,Human_miRNA_ID_2836193,Human_miRNA_ID_2841548,Human_miRNA_ID_2846610,Human_miRNA_ID_2849633,Human_miRNA_ID_2863743,Human_miRNA_ID_2890926,Human_miRNA_ID_3113475 RMVar_hsa_circ_77001,RMVar_hsa_circ_178244,RMVar_hsa_circ_79595,RMVar_hsa_circ_178252 37788 RMVar_ID_37788 Human_SNP_ID_601850094 A-to-I Human chr16 + 48352513 48352513 48352513 AAAAATATACAGGCGTGTTAGCATGTGCCTGTAATCCCAGCTTCTTGGGAAGCTGAGGCACAAGA AAAAATATACAGGCGTGTTAGCATGTGCCTGTGATCCCAGCTTCTTGGGAAGCTGAGGCACAAGA A G LONP2 Ensembl:ENSG00000102910 Protein coding 3'UTR GSE47997;GSE38233;GSE38233;GSE100210;GSE100210 K562 cells&HepG2 cells;cultured B-cells;cultured B-cells;HepG2 cell line;HepG2 cell line - 23474544,24183664,24183664,29129909,29129909 RNA-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 37789 RMVar_ID_37789 Human_SNP_ID_601850095 A-to-I Human chr16 + 48352513 48352513 48352513 AAAAATATACAGGCGTGTTAGCATGTGCCTGTAATCCCAGCTTCTTGGGAAGCTGAGGCACAAGA AAAAATATACAGGCGTGTTAGCATGTGCCTGTTATCCCAGCTTCTTGGGAAGCTGAGGCACAAGA A T LONP2 Ensembl:ENSG00000102910 Protein coding 3'UTR GSE47997;GSE38233;GSE38233;GSE100210;GSE100210 K562 cells&HepG2 cells;cultured B-cells;cultured B-cells;HepG2 cell line;HepG2 cell line - 23474544,24183664,24183664,29129909,29129909 RNA-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 37790 RMVar_ID_37790 Human_SNP_ID_601850266 A-to-I Human chr16 + 48353264 48353264 48353264 ATGGTGGCTCACGCCTGTAACCCTAGCACTTTAGGAAATCGAGGCGAGTGGATCACTTAAGCTCA ATGGTGGCTCACGCCTGTAACCCTAGCACTTTGGGAAATCGAGGCGAGTGGATCACTTAAGCTCA A G LONP2 Ensembl:ENSG00000102910 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1132063 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12745206 Human_miRNA_ID_1189160,Human_miRNA_ID_1471888,Human_miRNA_ID_1943186,Human_miRNA_ID_1946232,Human_miRNA_ID_2117377,Human_miRNA_ID_2200959,Human_miRNA_ID_2204022,Human_miRNA_ID_2816481,Human_miRNA_ID_2863744,Human_miRNA_ID_3113476 RMVar_hsa_circ_77001,RMVar_hsa_circ_178244,RMVar_hsa_circ_79595,RMVar_hsa_circ_178252 37791 RMVar_ID_37791 Human_SNP_ID_601850278 A-to-I Human chr16 + 48353304 48353304 48353304 GAGGCGAGTGGATCACTTAAGCTCAGGAGTTCAAGGCCAGCCTGGGCAACATGGCAAAACCCCAT GAGGCGAGTGGATCACTTAAGCTCAGGAGTTCGAGGCCAGCCTGGGCAACATGGCAAAACCCCAT A G LONP2 Ensembl:ENSG00000102910 Protein coding 3'UTR GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-Seq:(High) rs1140176 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22939739 RMVar_hsa_circ_77001,RMVar_hsa_circ_178244,RMVar_hsa_circ_79595,RMVar_hsa_circ_178252 37792 RMVar_ID_37792 Human_SNP_ID_601850287 A-to-I Human chr16 + 48353327 48353327 48353327 CAGGAGTTCAAGGCCAGCCTGGGCAACATGGCAAAACCCCATTTCTACAAAAAATACAAAAATTA CAGGAGTTCAAGGCCAGCCTGGGCAACATGGCGAAACCCCATTTCTACAAAAAATACAAAAATTA A G LONP2 Ensembl:ENSG00000102910 Protein coding 3'UTR GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs1140177 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_645096 RMVar_hsa_circ_77001,RMVar_hsa_circ_178244,RMVar_hsa_circ_79595,RMVar_hsa_circ_178252 37793 RMVar_ID_37793 Human_SNP_ID_601850288 A-to-I Human chr16 + 48353335 48353335 48353335 CAAGGCCAGCCTGGGCAACATGGCAAAACCCCATTTCTACAAAAAATACAAAAATTAGCTGGGCA CAAGGCCAGCCTGGGCAACATGGCAAAACCCCGTTTCTACAAAAAATACAAAAATTAGCTGGGCA A G LONP2 Ensembl:ENSG00000102910 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1132076 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_645096,Human_miRNA_ID_1657709 RMVar_hsa_circ_77001,RMVar_hsa_circ_178244,RMVar_hsa_circ_79595,RMVar_hsa_circ_178252 37794 RMVar_ID_37794 Human_SNP_ID_601850293 A-to-I Human chr16 + 48353353 48353353 48353353 CATGGCAAAACCCCATTTCTACAAAAAATACAAAAATTAGCTGGGCATGGTGGCACCCGCCTGTA CATGGCAAAACCCCATTTCTACAAAAAATACAGAAATTAGCTGGGCATGGTGGCACCCGCCTGTA A G LONP2 Ensembl:ENSG00000102910 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1132081 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_182523 RMVar_hsa_circ_77001,RMVar_hsa_circ_178244,RMVar_hsa_circ_79595,RMVar_hsa_circ_178252 37795 RMVar_ID_37795 Human_SNP_ID_601850298 A-to-I Human chr16 + 48353385 48353385 48353385 AAAATTAGCTGGGCATGGTGGCACCCGCCTGTAGTCCAGCTACTTGAGGCTGAGATGGGAGGATG AAAATTAGCTGGGCATGGTGGCACCCGCCTGTCGTCCAGCTACTTGAGGCTGAGATGGGAGGATG A C LONP2 Ensembl:ENSG00000102910 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-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 37796 RMVar_ID_37796 Human_SNP_ID_601850299 A-to-I Human chr16 + 48353385 48353385 48353385 AAAATTAGCTGGGCATGGTGGCACCCGCCTGTAGTCCAGCTACTTGAGGCTGAGATGGGAGGATG AAAATTAGCTGGGCATGGTGGCACCCGCCTGTGGTCCAGCTACTTGAGGCTGAGATGGGAGGATG A G LONP2 Ensembl:ENSG00000102910 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-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 37797 RMVar_ID_37797 Human_SNP_ID_601850300 A-to-I Human chr16 + 48353390 48353390 48353390 TAGCTGGGCATGGTGGCACCCGCCTGTAGTCCAGCTACTTGAGGCTGAGATGGGAGGATGAGGGA TAGCTGGGCATGGTGGCACCCGCCTGTAGTCCGGCTACTTGAGGCTGAGATGGGAGGATGAGGGA A G LONP2 Ensembl:ENSG00000102910 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947112714 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77001,RMVar_hsa_circ_178244,RMVar_hsa_circ_79595,RMVar_hsa_circ_178252 37798 RMVar_ID_37798 Human_SNP_ID_601850323 A-to-I Human chr16 + 48353439 48353439 48353439 ATGGGAGGATGAGGGAGGTCGGGGCTGCAGTGAGCCAAGATCACGCCACTGCACTCCAGCACCCT ATGGGAGGATGAGGGAGGTCGGGGCTGCAGTGGGCCAAGATCACGCCACTGCACTCCAGCACCCT A G LONP2 Ensembl:ENSG00000102910 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1056998608 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22939740,Human_RBP_ID_25212364 RMVar_hsa_circ_77001,RMVar_hsa_circ_178244,RMVar_hsa_circ_79595,RMVar_hsa_circ_178252 37799 RMVar_ID_37799 Human_SNP_ID_601850326 A-to-I Human chr16 + 48353443 48353443 48353443 GAGGATGAGGGAGGTCGGGGCTGCAGTGAGCCAAGATCACGCCACTGCACTCCAGCACCCTGGGC GAGGATGAGGGAGGTCGGGGCTGCAGTGAGCCCAGATCACGCCACTGCACTCCAGCACCCTGGGC A C LONP2 Ensembl:ENSG00000102910 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1132101 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22939740,Human_RBP_ID_25212364 RMVar_hsa_circ_77001,RMVar_hsa_circ_178244,RMVar_hsa_circ_79595,RMVar_hsa_circ_178252 37800 RMVar_ID_37800 Human_SNP_ID_601850327 A-to-I Human chr16 + 48353443 48353443 48353443 GAGGATGAGGGAGGTCGGGGCTGCAGTGAGCCAAGATCACGCCACTGCACTCCAGCACCCTGGGC GAGGATGAGGGAGGTCGGGGCTGCAGTGAGCCGAGATCACGCCACTGCACTCCAGCACCCTGGGC A G LONP2 Ensembl:ENSG00000102910 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1132101 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22939740,Human_RBP_ID_25212364 RMVar_hsa_circ_77001,RMVar_hsa_circ_178244,RMVar_hsa_circ_79595,RMVar_hsa_circ_178252 37801 RMVar_ID_37801 Human_SNP_ID_601850652 A-to-I Human chr16 + 48354263 48354263 48354263 GGAGTCTTGCTCTGTTACCCAGGCTGCACTGCAGTGGCATGATCTCGGCTCACTGCAACCTCTGC GGAGTCTTGCTCTGTTACCCAGGCTGCACTGCGGTGGCATGATCTCGGCTCACTGCAACCTCTGC A G LONP2 Ensembl:ENSG00000102910 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs896623070 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8185852,Human_RBP_ID_22370200,Human_RBP_ID_26441477 Human_miRNA_ID_1489486 37802 RMVar_ID_37802 Human_SNP_ID_601850688 A-to-I Human chr16 + 48354448 48354448 48354448 CCAGGCTGGTCTCAAACTCCCAACCTCAAATGATCCGGCCACCTTGGCCTCCCAAAATGCTGGCA CCAGGCTGGTCTCAAACTCCCAACCTCAAATGTTCCGGCCACCTTGGCCTCCCAAAATGCTGGCA A T LONP2 Ensembl:ENSG00000102910 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1401413081 Functional Loss SNV dbSNP153 33..33 33 - - - 37803 RMVar_ID_37803 Human_SNP_ID_601897925 A-to-I Human chr16 - 48546021 48546021 48546021 TTAAAAAAATTATTTTTTTTTTTTTTGAGACAAGGTCTTCCTCTGTCACCGAGGCTGGAATGCAG TTAAAAAAATTATTTTTTTTTTTTTTGAGACAGGGTCTTCCTCTGTCACCGAGGCTGGAATGCAG T C N4BP1 Ensembl:ENSG00000102921 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1402886688 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12746141 RMVar_hsa_circ_95913,RMVar_hsa_circ_126328,RMVar_hsa_circ_178256,RMVar_hsa_circ_89968,RMVar_hsa_circ_178257,RMVar_hsa_circ_178255 37804 RMVar_ID_37804 Human_SNP_ID_601911732 A-to-I Human chr16 - 48605101 48605101 48605101 TTGAACCAGGGAAGCGGAGGTTGCGGTGAACCAAGATCACGCTATTGCACTCCAGCCTGGGCAAC TTGAACCAGGGAAGCGGAGGTTGCGGTGAACCCAGATCACGCTATTGCACTCCAGCCTGGGCAAC T G N4BP1 Ensembl:ENSG00000102921 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444206909 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89968,RMVar_hsa_circ_178255 37805 RMVar_ID_37805 Human_SNP_ID_602288146 A-to-I Human chr16 + 50105206 50105206 50105206 TGTACATTCTGTAAAAACTTCAAAACCTGGCCAGGCATGGTGGCTCACGCCTATAATCCCAGCAC TGTACATTCTGTAAAAACTTCAAAACCTGGCCGGGCATGGTGGCTCACGCCTATAATCCCAGCAC A G HEATR3 Ensembl:ENSG00000155393 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1283372770 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17690433,Human_RBP_ID_21888602,Human_RBP_ID_27560226 Human_miRNA_ID_1697667 37806 RMVar_ID_37806 Human_SNP_ID_602288152 A-to-I Human chr16 + 50105226 50105226 50105226 CAAAACCTGGCCAGGCATGGTGGCTCACGCCTATAATCCCAGCACCTTGGGAGACCGAGGCGGGT CAAAACCTGGCCAGGCATGGTGGCTCACGCCTGTAATCCCAGCACCTTGGGAGACCGAGGCGGGT A G HEATR3 Ensembl:ENSG00000155393 Protein coding 3'UTR GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs2356839 Functional Loss SNV dbSNP153 33..33 33 - - - 37807 RMVar_ID_37807 Human_SNP_ID_602288174 A-to-I Human chr16 + 50105274 50105274 50105274 GGGAGACCGAGGCGGGTGGATCACTTGAGGTCAGGAGTTTGAGGCCAGCCTGGCCAACATGGTGA GGGAGACCGAGGCGGGTGGATCACTTGAGGTCTGGAGTTTGAGGCCAGCCTGGCCAACATGGTGA A T HEATR3 Ensembl:ENSG00000155393 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs532961800 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_128707,Human_RBP_ID_26441567 37808 RMVar_ID_37808 Human_SNP_ID_602288294 A-to-I Human chr16 + 50105606 50105606 50105606 ATGGAGTCTCACTGCTGCCCAGGCTGTATTACAGTGCTGCGATCTTGGCTTACTGCAACCTCTGC ATGGAGTCTCACTGCTGCCCAGGCTGTATTACGGTGCTGCGATCTTGGCTTACTGCAACCTCTGC A G HEATR3 Ensembl:ENSG00000155393 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170210494 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22370201,Human_RBP_ID_26441571 37809 RMVar_ID_37809 Human_SNP_ID_602288300 A-to-I Human chr16 + 50105615 50105615 50105615 CACTGCTGCCCAGGCTGTATTACAGTGCTGCGATCTTGGCTTACTGCAACCTCTGCCATTCCAGG CACTGCTGCCCAGGCTGTATTACAGTGCTGCGGTCTTGGCTTACTGCAACCTCTGCCATTCCAGG A G HEATR3 Ensembl:ENSG00000155393 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs532010759 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22370201,Human_RBP_ID_23164469 37810 RMVar_ID_37810 Human_SNP_ID_602288312 A-to-I Human chr16 + 50105669 50105669 50105669 GCCATTCCAGGTTCAAGCGATTCTCATGCCTCAGCCTCCTGAGTAGCTGGAATTACAGGCACCCA GCCATTCCAGGTTCAAGCGATTCTCATGCCTCCGCCTCCTGAGTAGCTGGAATTACAGGCACCCA A C HEATR3 Ensembl:ENSG00000155393 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1313406951 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23164471 37811 RMVar_ID_37811 Human_SNP_ID_602288313 A-to-I Human chr16 + 50105669 50105669 50105669 GCCATTCCAGGTTCAAGCGATTCTCATGCCTCAGCCTCCTGAGTAGCTGGAATTACAGGCACCCA GCCATTCCAGGTTCAAGCGATTCTCATGCCTCGGCCTCCTGAGTAGCTGGAATTACAGGCACCCA A G HEATR3 Ensembl:ENSG00000155393 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1313406951 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23164471 37812 RMVar_ID_37812 Human_SNP_ID_602288358 A-to-I Human chr16 + 50105832 50105832 50105832 ACCTCAAGTGATCCGCCTGCCCTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGTGC ACCTCAAGTGATCCGCCTGCCCTGGCCTCCCAGAGTGCTGGGATTACAGGCATGAGCCACCGTGC A G HEATR3 Ensembl:ENSG00000155393 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984529741 Functional Loss SNV dbSNP153 33..33 33 - - - 37813 RMVar_ID_37813 Human_SNP_ID_602303537 A-to-I Human chr16 + 50164413 50164413 50164413 CTCACTGCAAGCCCCGCCACCCAAGTTCAAGCAATTTTCTGCCTCAGCCTCCCGAGTAGCTGGGA CTCACTGCAAGCCCCGCCACCCAAGTTCAAGCTATTTTCTGCCTCAGCCTCCCGAGTAGCTGGGA A T TENT4B Ensembl:ENSG00000121274 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs146244470 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25213135 GWAS_ID_4322,GWAS_ID_4323,GWAS_ID_4324,GWAS_ID_4325,GWAS_ID_4326 37814 RMVar_ID_37814 Human_SNP_ID_602307072 A-to-I Human chr16 + 50178384 50178384 50178384 GGAGGATTGCTTGAGCCCTGGAGGTTGAGGCTACATGAGCCATGATCGCACCACTGTACTCCAGC GGAGGATTGCTTGAGCCCTGGAGGTTGAGGCTGCATGAGCCATGATCGCACCACTGTACTCCAGC A G TENT4B Ensembl:ENSG00000121274 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251252079 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17564134,Human_RBP_ID_25213196 37815 RMVar_ID_37815 Human_SNP_ID_603048003 A-to-I Human chr16 - 53040353 53040353 53040353 AATCAAATCAGGGGCTGGGCACAGTGGCTTACACCTGTAATCCCAGCACTTTGGGAGGCCACGGT AATCAAATCAGGGGCTGGGCACAGTGGCTTACGCCTGTAATCCCAGCACTTTGGGAGGCCACGGT T C AC007906.2 Ensembl:ENSG00000277639 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs750059960 Functional Loss SNV dbSNP153 33..33 33 - - - 37816 RMVar_ID_37816 Human_SNP_ID_603049218 A-to-I Human chr16 - 53045241 53045241 53045241 TAGCATACTGATAAAGAGACAGGATGGCTTATACCTGTAATCTCAACACTTTGGAAAGCTGAACA TAGCATACTGATAAAGAGACAGGATGGCTTATGCCTGTAATCTCAACACTTTGGAAAGCTGAACA T C AC007906.2 Ensembl:ENSG00000277639 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1298043480 Functional Loss SNV dbSNP153 33..33 33 - - - 37817 RMVar_ID_37817 Human_SNP_ID_603049882 A-to-I Human chr16 - 53048294 53048292 53048295 TTCCAGTGACCTCCCACTGCAGCCACTGTAGTAGCTGGGACTGCAGGCACATGCCACCACACCCA TTCCAGTGACCTCCCACTGCAGCCACTGTAG___CTGGGACTGCAGGCACATGCCACCACACCCA GCTA G AC007906.2 Ensembl:ENSG00000277639 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1472333092 Functional Loss DEL dbSNP153 32..34 33 - - - 37818 RMVar_ID_37818 Human_SNP_ID_603052446 A-to-I Human chr16 + 53058190 53058190 53058190 TCTCCCAGGCTGGAGTGCAGTGGCACGATGTCAGCTCACTGCAGTCTCCACCTCTGGAGTTCAAG TCTCCCAGGCTGGAGTGCAGTGGCACGATGTCGGCTCACTGCAGTCTCCACCTCTGGAGTTCAAG A G CHD9 Ensembl:ENSG00000177200 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1320670960 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6518506 RMVar_hsa_circ_110606,RMVar_hsa_circ_178346 37819 RMVar_ID_37819 Human_SNP_ID_603052621 A-to-I Human chr16 + 53058928 53058928 53058928 GTCACCCATGCCTCCTGTAGTGGTATGATCATAGCTACTGCAGCCTCAACCTCCTGAGCTCGAGG GTCACCCATGCCTCCTGTAGTGGTATGATCATTGCTACTGCAGCCTCAACCTCCTGAGCTCGAGG A T CHD9 Ensembl:ENSG00000177200 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs367651314 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110606,RMVar_hsa_circ_178346 37820 RMVar_ID_37820 Human_SNP_ID_603052639 A-to-I Human chr16 + 53058992 53058992 53058992 GGATCCTCCCACCCAGCCAAGTAGCTGGGGCTACAGGTGCACACCATCATGCCCAGCTAATTTTT GGATCCTCCCACCCAGCCAAGTAGCTGGGGCTGCAGGTGCACACCATCATGCCCAGCTAATTTTT A G CHD9 Ensembl:ENSG00000177200 Protein coding intron GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs186034533 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110606,RMVar_hsa_circ_178346 37821 RMVar_ID_37821 Human_SNP_ID_603052934 A-to-I Human chr16 + 53060576 53060576 53060576 GTCTAGAAGTTCCAGACCAGCCTGGGCAACATAGCAAGACCCCATATCTACAAAAAAATGAAAAA GTCTAGAAGTTCCAGACCAGCCTGGGCAACATTGCAAGACCCCATATCTACAAAAAAATGAAAAA A T CHD9 Ensembl:ENSG00000177200 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs186439425 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110606,RMVar_hsa_circ_178346 37822 RMVar_ID_37822 Human_SNP_ID_603053770 A-to-I Human chr16 + 53063927 53063927 53063927 TGTGATCATAGCTCACTGAAGCTTAAACTCCTAGGCTCTGGCCATCCTCCCACCTCAGCCTCCAG TGTGATCATAGCTCACTGAAGCTTAAACTCCTGGGCTCTGGCCATCCTCCCACCTCAGCCTCCAG A G CHD9 Ensembl:ENSG00000177200 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs912204817 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110606,RMVar_hsa_circ_178346 37823 RMVar_ID_37823 Human_SNP_ID_603056718 A-to-I Human chr16 + 53076884 53076884 53076884 TTTTACAAGCAAGGTCTCAGTGGCAGGATCACAGCTCACTGCAGCCTTGAACTCCTAGGCTCAAA TTTTACAAGCAAGGTCTCAGTGGCAGGATCACGGCTCACTGCAGCCTTGAACTCCTAGGCTCAAA A G CHD9 Ensembl:ENSG00000177200 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1567310759 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12751289 RMVar_hsa_circ_110606,RMVar_hsa_circ_178346 37824 RMVar_ID_37824 Human_SNP_ID_603065537 A-to-I Human chr16 + 53113799 53113799 53113799 TGTAGCTCACTGCAGCCTCAAACTGAACTCCTAGGCGTAAGCGATTCTCTCACCTCAGCCTCCTG TGTAGCTCACTGCAGCCTCAAACTGAACTCCTTGGCGTAAGCGATTCTCTCACCTCAGCCTCCTG A T CHD9 Ensembl:ENSG00000177200 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs369681496 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110606,RMVar_hsa_circ_178346 37825 RMVar_ID_37825 Human_SNP_ID_603066645 A-to-I Human chr16 + 53118274 53118274 53118274 CCCTGTCTCTACCAAAAATACAAAAATTAGCTAGGTGTAGAGGTGCACACCTGTAATCCCAGCTA CCCTGTCTCTACCAAAAATACAAAAATTAGCTGGGTGTAGAGGTGCACACCTGTAATCCCAGCTA A G CHD9 Ensembl:ENSG00000177200 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1483098986 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110606,RMVar_hsa_circ_178346 37826 RMVar_ID_37826 Human_SNP_ID_603072213 A-to-I Human chr16 + 53140662 53140662 53140662 GTGCTGGAGTGCAGTAGCATCGATCGTAGCTCACTGCATCCTCAACCTCCTGAGCTCAAATGATT GTGCTGGAGTGCAGTAGCATCGATCGTAGCTCGCTGCATCCTCAACCTCCTGAGCTCAAATGATT A G CHD9 Ensembl:ENSG00000177200 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1294930170 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110606,RMVar_hsa_circ_178346 37827 RMVar_ID_37827 Human_SNP_ID_603080253 A-to-I Human chr16 + 53174218 53174218 53174218 AGGTGAGAGGATCACTTGAGCCCAGGATGTTGAGGCTGCAGTGAACCAAGATCGTGCCACTACAG AGGTGAGAGGATCACTTGAGCCCAGGATGTTGGGGCTGCAGTGAACCAAGATCGTGCCACTACAG A G CHD9 Ensembl:ENSG00000177200 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1480311797 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6518705 RMVar_hsa_circ_77604,RMVar_hsa_circ_178349,RMVar_hsa_circ_335782,RMVar_hsa_circ_352579,RMVar_hsa_circ_367103,RMVar_hsa_circ_348262,RMVar_hsa_circ_178353,RMVar_hsa_circ_178355,RMVar_hsa_circ_5273,RMVar_hsa_circ_178354,RMVar_hsa_circ_178352 37828 RMVar_ID_37828 Human_SNP_ID_603080368 A-to-I Human chr16 + 53174807 53174803 53174807 TTTCATTTTATTTTTTCTAGAGATGCAGTCTTACTTTGTTGCCCGGGCTTGTTTTGAACTCCTTT TTTCATTTTATTTTTTCTAGAGATGCAGT____CTTTGTTGCCCGGGCTTGTTTTGAACTCCTTT TCTTA T CHD9 Ensembl:ENSG00000177200 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs905718188 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_12751826 RMVar_hsa_circ_77604,RMVar_hsa_circ_178349,RMVar_hsa_circ_335782,RMVar_hsa_circ_352579,RMVar_hsa_circ_367103,RMVar_hsa_circ_348262,RMVar_hsa_circ_178353,RMVar_hsa_circ_178355,RMVar_hsa_circ_5273,RMVar_hsa_circ_178354,RMVar_hsa_circ_178352 37829 RMVar_ID_37829 Human_SNP_ID_603081967 A-to-I Human chr16 + 53181893 53181890 53181894 CCTAGGGTCAAGAGTTTGAGACCAGCCTGGCCAACATGGTGAAACCCCAGCTCCATTAAAAGTAC CCTAGGGTCAAGAGTTTGAGACCAGCCTGG____CATGGTGAAACCCCAGCTCCATTAAAAGTAC GCCAA G CHD9 Ensembl:ENSG00000177200 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs998092330 Functional Loss DEL dbSNP153 31..34 33 - - - RMVar_hsa_circ_77604,RMVar_hsa_circ_178349,RMVar_hsa_circ_335782,RMVar_hsa_circ_352579,RMVar_hsa_circ_367103,RMVar_hsa_circ_348262,RMVar_hsa_circ_178353,RMVar_hsa_circ_178355,RMVar_hsa_circ_5273,RMVar_hsa_circ_178354,RMVar_hsa_circ_178352 37830 RMVar_ID_37830 Human_SNP_ID_603098707 A-to-I Human chr16 + 53255151 53255151 53255151 TGGGCAACATGGCAAGACCCTGTCTCTATAAAAAATAAAAATTAGCTGGGCATAATGGTGCATGC TGGGCAACATGGCAAGACCCTGTCTCTATAAAGAATAAAAATTAGCTGGGCATAATGGTGCATGC A G CHD9 Ensembl:ENSG00000177200 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388184683 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3587,RMVar_hsa_circ_352579,RMVar_hsa_circ_367103,RMVar_hsa_circ_5273,RMVar_hsa_circ_364202,RMVar_hsa_circ_73719,RMVar_hsa_circ_358410,RMVar_hsa_circ_344162,RMVar_hsa_circ_16723,RMVar_hsa_circ_10575,RMVar_hsa_circ_76512,RMVar_hsa_circ_362852,RMVar_hsa_circ_178371,RMVar_hsa_circ_25396,RMVar_hsa_circ_178372,RMVar_hsa_circ_178370,RMVar_hsa_circ_334427,RMVar_hsa_circ_60369,RMVar_hsa_circ_361537,RMVar_hsa_circ_310855,RMVar_hsa_circ_283874,RMVar_hsa_circ_178373,RMVar_hsa_circ_178374,RMVar_hsa_circ_61566,RMVar_hsa_circ_178384,RMVar_hsa_circ_98229,RMVar_hsa_circ_342151,RMVar_hsa_circ_276407,RMVar_hsa_circ_178385,RMVar_hsa_circ_282780,RMVar_hsa_circ_178383,RMVar_hsa_circ_356603,RMVar_hsa_circ_310283,RMVar_hsa_circ_355748,RMVar_hsa_circ_285338,RMVar_hsa_circ_105768,RMVar_hsa_circ_265691,RMVar_hsa_circ_25328,RMVar_hsa_circ_178389,RMVar_hsa_circ_178391,RMVar_hsa_circ_11591,RMVar_hsa_circ_178390,RMVar_hsa_circ_178388 37831 RMVar_ID_37831 Human_SNP_ID_603099845 A-to-I Human chr16 + 53260350 53260350 53260350 AAAAGTTAAAACTCAGCCAGGCAAGCTGGCATATGCTTGTTGTCCCAGCTACTTGGGAGGCTGAG AAAAGTTAAAACTCAGCCAGGCAAGCTGGCATTTGCTTGTTGTCCCAGCTACTTGGGAGGCTGAG A T CHD9 Ensembl:ENSG00000177200 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1340800476 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12752272 RMVar_hsa_circ_352579,RMVar_hsa_circ_367103,RMVar_hsa_circ_358410,RMVar_hsa_circ_344162,RMVar_hsa_circ_16723,RMVar_hsa_circ_76512,RMVar_hsa_circ_178371,RMVar_hsa_circ_25396,RMVar_hsa_circ_178372,RMVar_hsa_circ_334427,RMVar_hsa_circ_361537,RMVar_hsa_circ_310855,RMVar_hsa_circ_178373,RMVar_hsa_circ_178384,RMVar_hsa_circ_98229,RMVar_hsa_circ_342151,RMVar_hsa_circ_282780,RMVar_hsa_circ_178383,RMVar_hsa_circ_310283,RMVar_hsa_circ_285338,RMVar_hsa_circ_105768,RMVar_hsa_circ_265691,RMVar_hsa_circ_25328,RMVar_hsa_circ_126390,RMVar_hsa_circ_282908,RMVar_hsa_circ_178389,RMVar_hsa_circ_178391,RMVar_hsa_circ_11591,RMVar_hsa_circ_178390,RMVar_hsa_circ_301225,RMVar_hsa_circ_178388,RMVar_hsa_circ_287976,RMVar_hsa_circ_272695,RMVar_hsa_circ_278328,RMVar_hsa_circ_270492,RMVar_hsa_circ_178394,RMVar_hsa_circ_37398,RMVar_hsa_circ_42384,RMVar_hsa_circ_178396,RMVar_hsa_circ_29375,RMVar_hsa_circ_178397,RMVar_hsa_circ_178395,RMVar_hsa_circ_178392,RMVar_hsa_circ_178393 37832 RMVar_ID_37832 Human_SNP_ID_603107213 A-to-I Human chr16 + 53293357 53293357 53293357 AAATAAATAACTGGGCACAGTGGCTAATGCCTATAATCCCAGCACTTTGGGAGGCCGAGGTGGGA AAATAAATAACTGGGCACAGTGGCTAATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGA A G CHD9 Ensembl:ENSG00000177200 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs546030255 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25214430 RMVar_hsa_circ_16723,RMVar_hsa_circ_285338,RMVar_hsa_circ_265691,RMVar_hsa_circ_178391,RMVar_hsa_circ_11591,RMVar_hsa_circ_301225,RMVar_hsa_circ_37398,RMVar_hsa_circ_42384,RMVar_hsa_circ_29375,RMVar_hsa_circ_178397,RMVar_hsa_circ_68427,RMVar_hsa_circ_25491,RMVar_hsa_circ_349402,RMVar_hsa_circ_68768,RMVar_hsa_circ_57006,RMVar_hsa_circ_80422,RMVar_hsa_circ_326976,RMVar_hsa_circ_178403,RMVar_hsa_circ_358255,RMVar_hsa_circ_178404,RMVar_hsa_circ_268595 37833 RMVar_ID_37833 Human_SNP_ID_603107250 A-to-I Human chr16 + 53293517 53293517 53293517 GCATGCCTGTGGTCCCAGCCACTCGGGAGACTAAAGTGGGAGTATCACCTGAGCCCAGAAGGTCC GCATGCCTGTGGTCCCAGCCACTCGGGAGACTCAAGTGGGAGTATCACCTGAGCCCAGAAGGTCC A C CHD9 Ensembl:ENSG00000177200 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs183709959 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16723,RMVar_hsa_circ_285338,RMVar_hsa_circ_265691,RMVar_hsa_circ_178391,RMVar_hsa_circ_11591,RMVar_hsa_circ_301225,RMVar_hsa_circ_37398,RMVar_hsa_circ_42384,RMVar_hsa_circ_29375,RMVar_hsa_circ_178397,RMVar_hsa_circ_68427,RMVar_hsa_circ_25491,RMVar_hsa_circ_349402,RMVar_hsa_circ_68768,RMVar_hsa_circ_57006,RMVar_hsa_circ_80422,RMVar_hsa_circ_326976,RMVar_hsa_circ_178403,RMVar_hsa_circ_358255,RMVar_hsa_circ_178404,RMVar_hsa_circ_268595 37834 RMVar_ID_37834 Human_SNP_ID_603107251 A-to-I Human chr16 + 53293517 53293517 53293517 GCATGCCTGTGGTCCCAGCCACTCGGGAGACTAAAGTGGGAGTATCACCTGAGCCCAGAAGGTCC GCATGCCTGTGGTCCCAGCCACTCGGGAGACTGAAGTGGGAGTATCACCTGAGCCCAGAAGGTCC A G CHD9 Ensembl:ENSG00000177200 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs183709959 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16723,RMVar_hsa_circ_285338,RMVar_hsa_circ_265691,RMVar_hsa_circ_178391,RMVar_hsa_circ_11591,RMVar_hsa_circ_301225,RMVar_hsa_circ_37398,RMVar_hsa_circ_42384,RMVar_hsa_circ_29375,RMVar_hsa_circ_178397,RMVar_hsa_circ_68427,RMVar_hsa_circ_25491,RMVar_hsa_circ_349402,RMVar_hsa_circ_68768,RMVar_hsa_circ_57006,RMVar_hsa_circ_80422,RMVar_hsa_circ_326976,RMVar_hsa_circ_178403,RMVar_hsa_circ_358255,RMVar_hsa_circ_178404,RMVar_hsa_circ_268595 37835 RMVar_ID_37835 Human_SNP_ID_603112592 A-to-I Human chr16 + 53315618 53315618 53315618 CTCCCACCTCAGTCTCCTGAGTAGCTGGGACCACAGGTGCACACCACCATGCCCAGCTGACTTTT CTCCCACCTCAGTCTCCTGAGTAGCTGGGACCCCAGGTGCACACCACCATGCCCAGCTGACTTTT A C CHD9 Ensembl:ENSG00000177200 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs983996713 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_68768,RMVar_hsa_circ_57006,RMVar_hsa_circ_35720,RMVar_hsa_circ_178409,RMVar_hsa_circ_9342,RMVar_hsa_circ_11146,RMVar_hsa_circ_72471,RMVar_hsa_circ_340009,RMVar_hsa_circ_279394,RMVar_hsa_circ_355594,RMVar_hsa_circ_178412,RMVar_hsa_circ_178414,RMVar_hsa_circ_178416,RMVar_hsa_circ_81942,RMVar_hsa_circ_291623,RMVar_hsa_circ_178415 37836 RMVar_ID_37836 Human_SNP_ID_603112617 A-to-I Human chr16 + 53315700 53315700 53315700 AGGGTTTCACCATGTTGGCCAAGGCTGGTCTCAAACTCCTGGCCTCAAGCAATCCGCCTGCTCAG AGGGTTTCACCATGTTGGCCAAGGCTGGTCTCGAACTCCTGGCCTCAAGCAATCCGCCTGCTCAG A G CHD9 Ensembl:ENSG00000177200 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904701106 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_68768,RMVar_hsa_circ_57006,RMVar_hsa_circ_35720,RMVar_hsa_circ_178409,RMVar_hsa_circ_9342,RMVar_hsa_circ_11146,RMVar_hsa_circ_72471,RMVar_hsa_circ_340009,RMVar_hsa_circ_279394,RMVar_hsa_circ_355594,RMVar_hsa_circ_178412,RMVar_hsa_circ_178414,RMVar_hsa_circ_178416,RMVar_hsa_circ_81942,RMVar_hsa_circ_291623,RMVar_hsa_circ_178415 37837 RMVar_ID_37837 Human_SNP_ID_603112627 A-to-I Human chr16 + 53315731 53315731 53315731 CAAACTCCTGGCCTCAAGCAATCCGCCTGCTCAGCCTCCCAAAGTGCTAGGAATACAGACATGAA CAAACTCCTGGCCTCAAGCAATCCGCCTGCTCCGCCTCCCAAAGTGCTAGGAATACAGACATGAA A C CHD9 Ensembl:ENSG00000177200 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs780837498 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_68768,RMVar_hsa_circ_57006,RMVar_hsa_circ_35720,RMVar_hsa_circ_178409,RMVar_hsa_circ_9342,RMVar_hsa_circ_11146,RMVar_hsa_circ_72471,RMVar_hsa_circ_340009,RMVar_hsa_circ_279394,RMVar_hsa_circ_355594,RMVar_hsa_circ_178412,RMVar_hsa_circ_178414,RMVar_hsa_circ_178416,RMVar_hsa_circ_81942,RMVar_hsa_circ_291623,RMVar_hsa_circ_178415 37838 RMVar_ID_37838 Human_SNP_ID_603112879 A-to-I Human chr16 + 53317040 53317040 53317040 GGCAAACATGGTACCCCATCTCTACTAAAAATACAAAAATCAGCTGGGCATGGTGGCGGGTGCCT GGCAAACATGGTACCCCATCTCTACTAAAAATTCAAAAATCAGCTGGGCATGGTGGCGGGTGCCT A T CHD9 Ensembl:ENSG00000177200 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs974369306 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_68768,RMVar_hsa_circ_57006,RMVar_hsa_circ_35720,RMVar_hsa_circ_178409,RMVar_hsa_circ_9342,RMVar_hsa_circ_11146,RMVar_hsa_circ_72471,RMVar_hsa_circ_340009,RMVar_hsa_circ_279394,RMVar_hsa_circ_355594,RMVar_hsa_circ_178412,RMVar_hsa_circ_178414,RMVar_hsa_circ_178416,RMVar_hsa_circ_81942,RMVar_hsa_circ_291623,RMVar_hsa_circ_178415 37839 RMVar_ID_37839 Human_SNP_ID_603113105 A-to-I Human chr16 + 53317953 53317953 53317953 GTAGCACACACCTGTAGTCCCAGCTACTTGAGAGGCTGAGGTGGGAGGATCACTTGAGCCTGGGA GTAGCACACACCTGTAGTCCCAGCTACTTGAGCGGCTGAGGTGGGAGGATCACTTGAGCCTGGGA A C CHD9 Ensembl:ENSG00000177200 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs12924399 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_68768,RMVar_hsa_circ_57006,RMVar_hsa_circ_35720,RMVar_hsa_circ_178409,RMVar_hsa_circ_9342,RMVar_hsa_circ_11146,RMVar_hsa_circ_72471,RMVar_hsa_circ_340009,RMVar_hsa_circ_279394,RMVar_hsa_circ_355594,RMVar_hsa_circ_178412,RMVar_hsa_circ_178414,RMVar_hsa_circ_178416,RMVar_hsa_circ_81942,RMVar_hsa_circ_291623,RMVar_hsa_circ_178415 37840 RMVar_ID_37840 Human_SNP_ID_603113116 A-to-I Human chr16 + 53318020 53318020 53318020 TGAAGGCTCCAGTGAGCTGTGACCACACCACTATTCTCCAGCCTGGGCAACAGAGCAAGACCCTG TGAAGGCTCCAGTGAGCTGTGACCACACCACTCTTCTCCAGCCTGGGCAACAGAGCAAGACCCTG A C CHD9 Ensembl:ENSG00000177200 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs754370758 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25214570 RMVar_hsa_circ_68768,RMVar_hsa_circ_57006,RMVar_hsa_circ_35720,RMVar_hsa_circ_178409,RMVar_hsa_circ_9342,RMVar_hsa_circ_11146,RMVar_hsa_circ_72471,RMVar_hsa_circ_340009,RMVar_hsa_circ_279394,RMVar_hsa_circ_355594,RMVar_hsa_circ_178412,RMVar_hsa_circ_178414,RMVar_hsa_circ_178416,RMVar_hsa_circ_81942,RMVar_hsa_circ_291623,RMVar_hsa_circ_178415 37841 RMVar_ID_37841 Human_SNP_ID_603113117 A-to-I Human chr16 + 53318020 53318020 53318020 TGAAGGCTCCAGTGAGCTGTGACCACACCACTATTCTCCAGCCTGGGCAACAGAGCAAGACCCTG TGAAGGCTCCAGTGAGCTGTGACCACACCACTGTTCTCCAGCCTGGGCAACAGAGCAAGACCCTG A G CHD9 Ensembl:ENSG00000177200 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs754370758 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25214570 RMVar_hsa_circ_68768,RMVar_hsa_circ_57006,RMVar_hsa_circ_35720,RMVar_hsa_circ_178409,RMVar_hsa_circ_9342,RMVar_hsa_circ_11146,RMVar_hsa_circ_72471,RMVar_hsa_circ_340009,RMVar_hsa_circ_279394,RMVar_hsa_circ_355594,RMVar_hsa_circ_178412,RMVar_hsa_circ_178414,RMVar_hsa_circ_178416,RMVar_hsa_circ_81942,RMVar_hsa_circ_291623,RMVar_hsa_circ_178415 37842 RMVar_ID_37842 Human_SNP_ID_603114879 A-to-I Human chr16 - 53325856 53325856 53325856 GGAATATTTCCATGACATAAAACACAAATAGAAATCTACACAAAGAAAGCAAACAAACAATTTCT GGAATATTTCCATGACATAAAACACAAATAGAGATCTACACAAAGAAAGCAAACAAACAATTTCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs545565392 Functional Loss SNV dbSNP153 33..33 33 - - - 37843 RMVar_ID_37843 Human_SNP_ID_603157693 A-to-I Human chr16 - 53496663 53496663 53496663 CACCCGGCTAATTTTTGTAGTTTTAGTAAGAGACTGGATTTCACCATGTTGGCTAGGCTGGTCTC CACCCGGCTAATTTTTGTAGTTTTAGTAAGAGGCTGGATTTCACCATGTTGGCTAGGCTGGTCTC T C AKTIP Ensembl:ENSG00000166971 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs571973315 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_321096,RMVar_hsa_circ_20428,RMVar_hsa_circ_66267 37844 RMVar_ID_37844 Human_SNP_ID_603205079 A-to-I Human chr16 - 53694374 53694374 53694374 GGAGTGCAGTGGTAAGATCTCGGCTCACTGCAACCTTCGCCTCCCGGGTTCAAGTGATTCTCCTG GGAGTGCAGTGGTAAGATCTCGGCTCACTGCAGCCTTCGCCTCCCGGGTTCAAGTGATTCTCCTG T C RPGRIP1L Ensembl:ENSG00000103494 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1047546507 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91797,RMVar_hsa_circ_178453,RMVar_hsa_circ_53417,RMVar_hsa_circ_376753 37845 RMVar_ID_37845 Human_SNP_ID_603214080 A-to-I Human chr16 + 53731923 53731923 53731923 GCTGTTTGTACTTTTTGTAGAGACAGGGTTTCACCATGTTGGCCCGGCTGGTCTCAAACTCCTAA GCTGTTTGTACTTTTTGTAGAGACAGGGTTTCGCCATGTTGGCCCGGCTGGTCTCAAACTCCTAA A G FTO Ensembl:ENSG00000140718 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1269901708 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12753623 37846 RMVar_ID_37846 Human_SNP_ID_603236354 A-to-I Human chr16 + 53830775 53830775 53830775 AAAATAAGCTGGGCATGGTGGTGCGCACCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGTAGA AAAATAAGCTGGGCATGGTGGTGCGCACCTGTGGTCCCAGCTACTCGGGAGGCTGAGGCAGTAGA A G FTO Ensembl:ENSG00000140718 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984913610 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_178462,RMVar_hsa_circ_333054,RMVar_hsa_circ_340040,RMVar_hsa_circ_344665,RMVar_hsa_circ_178464,RMVar_hsa_circ_291788,RMVar_hsa_circ_178463,RMVar_hsa_circ_321193,RMVar_hsa_circ_25239 37847 RMVar_ID_37847 Human_SNP_ID_603271647 A-to-I Human chr16 + 53984422 53984422 53984422 ATGGCTCACTGCAGACTCGACCTCCCCAGCTCAAGTGATCCTCCCACCTCAGCCTCCTGAGTAGC ATGGCTCACTGCAGACTCGACCTCCCCAGCTCGAGTGATCCTCCCACCTCAGCCTCCTGAGTAGC A G FTO Ensembl:ENSG00000140718 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs564247754 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104875,RMVar_hsa_circ_178474,RMVar_hsa_circ_101702,RMVar_hsa_circ_178475 37848 RMVar_ID_37848 Human_SNP_ID_603300256 A-to-I Human chr16 + 54113973 54113973 54113973 GGGACTACAGGCACGTGCCACCACGCCCAGCTAATTTTTGTATTTTTAGCAGAGATGGGGTTTCA GGGACTACAGGCACGTGCCACCACGCCCAGCTGATTTTTGTATTTTTAGCAGAGATGGGGTTTCA A G FTO Ensembl:ENSG00000140718 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1408390195 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9841680 RMVar_hsa_circ_104875,RMVar_hsa_circ_178474,RMVar_hsa_circ_101702,RMVar_hsa_circ_178475,RMVar_hsa_circ_86084,RMVar_hsa_circ_178487 37849 RMVar_ID_37849 Human_SNP_ID_603373724 A-to-I Human chr16 + 54395253 54395253 54395253 ACTTTGGGATTCCATAACAAAAATTGTAGACTAGATGTCTCAAACAACATAAATTTACTTTCTTA ACTTTGGGATTCCATAACAAAAATTGTAGACTTGATGTCTCAAACAACATAAATTTACTTTCTTA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277252569 Functional Loss SNV dbSNP153 33..33 33 - - - 37850 RMVar_ID_37850 Human_SNP_ID_603507578 A-to-I Human chr16 - 54918957 54918957 54918957 ACCAAATATATTTTGTTTAGCCAAGGTATAGGAAAAATAAAATAAATTGTATAGGTTGACTTTTT ACCAAATATATTTTGTTTAGCCAAGGTATAGGGAAAATAAAATAAATTGTATAGGTTGACTTTTT T C CRNDE Ensembl:ENSG00000245694 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs191597929 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_475536,Human_RBP_ID_1527143,Human_RBP_ID_1843590,Human_RBP_ID_9062911,Human_RBP_ID_9842976,Human_RBP_ID_18680725,Human_RBP_ID_22370203,Human_RBP_ID_23692678,Human_RBP_ID_25215612 Human_miRNA_ID_3175840 37851 RMVar_ID_37851 Human_SNP_ID_603508685 A-to-I Human chr16 - 54923581 54923581 54923581 TGGAAGGAGGAGATTCTGAAGATAAGGAGGTAATATTATCTCTTTTAAAAGAATACTTTCCTCTG TGGAAGGAGGAGATTCTGAAGATAAGGAGGTAGTATTATCTCTTTTAAAAGAATACTTTCCTCTG T C CRNDE Ensembl:ENSG00000245694 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1216919838 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1519312,Human_RBP_ID_22944445,Human_RBP_ID_26329031,Human_RBP_ID_27811125 Human_Splice_Rec_1714104,Human_Splice_Rec_1714118,Human_Splice_Rec_1714124,Human_Splice_Rec_1714132,Human_Splice_Rec_1714140,Human_Splice_Rec_1714148,Human_Splice_Rec_1714156,Human_Splice_Rec_1714166,Human_Splice_Rec_1714174,Human_Splice_Rec_1714184,Human_Splice_Rec_1714192,Human_Splice_Rec_1714200,Human_Splice_Rec_1714206 37852 RMVar_ID_37852 Human_SNP_ID_603869702 A-to-I Human chr16 - 56362589 56362589 56362589 GAGCAGTCGCCTGCCTGCAGCAGGCAGCTTCTACTCCTGCCTCATGCGTACGTCCCACAAATGCA GAGCAGTCGCCTGCCTGCAGCAGGCAGCTTCTGCTCCTGCCTCATGCGTACGTCCCACAAATGCA T C AMFR Ensembl:ENSG00000159461 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1273357329 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4372894,Human_RBP_ID_5142489,Human_RBP_ID_9285024,Human_RBP_ID_18680784,Human_RBP_ID_23692897 Human_miRNA_ID_1220317 RMVar_hsa_circ_107159,RMVar_hsa_circ_117430,RMVar_hsa_circ_178520,RMVar_hsa_circ_178521 37853 RMVar_ID_37853 Human_SNP_ID_603887544 A-to-I Human chr16 - 56435248 56435248 56435248 ATGGTGGCGCATGCCTGTAATCTCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCTG ATGGTGGCGCATGCCTGTAATCTCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCTG T C NUDT21 Ensembl:ENSG00000167005 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs574187944 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87420,RMVar_hsa_circ_178547,RMVar_hsa_circ_363898,RMVar_hsa_circ_13563 37854 RMVar_ID_37854 Human_SNP_ID_603893115 A-to-I Human chr16 + 56457778 56457778 56457778 TCTCAGCTCACTGCAACCTCCGCCTCCAGGTTAAAATGATTCTCCTGCCTCAGCCTCCCGAGTAG TCTCAGCTCACTGCAACCTCCGCCTCCAGGTTGAAATGATTCTCCTGCCTCAGCCTCCCGAGTAG A G OGFOD1 Ensembl:ENSG00000087263 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904672353 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_178548,RMVar_hsa_circ_330085,RMVar_hsa_circ_69200 37855 RMVar_ID_37855 Human_SNP_ID_603896480 A-to-I Human chr16 + 56471255 56471255 56471255 ATGGTGGTGAACGCCTGTAATCCAAGCTACTCAGGAGGCTGAGGTGGAAGAATCACTTGAACCGG ATGGTGGTGAACGCCTGTAATCCAAGCTACTCGGGAGGCTGAGGTGGAAGAATCACTTGAACCGG A G OGFOD1 Ensembl:ENSG00000087263 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1185424269 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_178551,RMVar_hsa_circ_98818,RMVar_hsa_circ_114582,RMVar_hsa_circ_178560,RMVar_hsa_circ_112805,RMVar_hsa_circ_110916,RMVar_hsa_circ_178557,RMVar_hsa_circ_178558,RMVar_hsa_circ_82847,RMVar_hsa_circ_178561 37856 RMVar_ID_37856 Human_SNP_ID_603901952 A-to-I Human chr16 - 56493262 56493262 56493262 CTCACCTCAGCCTCCTGAGTAGATGGGACTAAAGGCATGAGCCACCAGCCCGGCTAATTTTTTAT CTCACCTCAGCCTCCTGAGTAGATGGGACTAACGGCATGAGCCACCAGCCCGGCTAATTTTTTAT T G BBS2 Ensembl:ENSG00000125124 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1403934336 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_178568,RMVar_hsa_circ_178564,RMVar_hsa_circ_265566,RMVar_hsa_circ_178569,RMVar_hsa_circ_178570,RMVar_hsa_circ_178566,RMVar_hsa_circ_178567 37857 RMVar_ID_37857 Human_SNP_ID_603948073 A-to-I Human chr16 - 56666906 56666906 56666906 AAGTGTGCCCAGGGCTGCATCTGCAAAGGGGCATCGGAGAAGTGCAGCTGCTGCGCCTGATGTCG AAGTGTGCCCAGGGCTGCATCTGCAAAGGGGCGTCGGAGAAGTGCAGCTGCTGCGCCTGATGTCG T C MT1G Ensembl:ENSG00000125144 Protein coding CDS GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs755439641 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_128495,Human_RBP_ID_5113533,Human_RBP_ID_17653052,Human_RBP_ID_22442052 Human_Splice_Rec_1715902,Human_Splice_Rec_1715906,Human_Splice_Rec_1715908 Human_miRNA_ID_41647,Human_miRNA_ID_70365,Human_miRNA_ID_364168,Human_miRNA_ID_378554,Human_miRNA_ID_485298,Human_miRNA_ID_598185 37858 RMVar_ID_37858 Human_SNP_ID_603986066 A-to-I Human chr16 + 56822700 56822700 56822700 CTCCTACCTCGGCCTCCCGAGTAGCTGGGACTACAGGCACCTGCCACCATGCCTGGTTAATTTTT CTCCTACCTCGGCCTCCCGAGTAGCTGGGACTGCAGGCACCTGCCACCATGCCTGGTTAATTTTT A G NUP93 Ensembl:ENSG00000102900 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1276737806 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17414,RMVar_hsa_circ_178593,RMVar_hsa_circ_87593,RMVar_hsa_circ_103358,RMVar_hsa_circ_77865,RMVar_hsa_circ_178594,RMVar_hsa_circ_343502,RMVar_hsa_circ_178592,RMVar_hsa_circ_18118,RMVar_hsa_circ_127700,RMVar_hsa_circ_178595,RMVar_hsa_circ_92014,RMVar_hsa_circ_178598,RMVar_hsa_circ_178599,RMVar_hsa_circ_178600,RMVar_hsa_circ_286082 37859 RMVar_ID_37859 Human_SNP_ID_603990667 A-to-I Human chr16 + 56840160 56840160 56840160 CTCCTGCCTCAGCCTCACGAGTAGCTGGGACTACAGGTGCCCGCCAACACGCCCAGCTAATTTTT CTCCTGCCTCAGCCTCACGAGTAGCTGGGACTGCAGGTGCCCGCCAACACGCCCAGCTAATTTTT A G NUP93 Ensembl:ENSG00000102900 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs528738867 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_369307,RMVar_hsa_circ_178604,RMVar_hsa_circ_94937,RMVar_hsa_circ_178607,RMVar_hsa_circ_178608,RMVar_hsa_circ_178610,RMVar_hsa_circ_325460 37860 RMVar_ID_37860 Human_SNP_ID_603990823 A-to-I Human chr16 + 56840738 56840738 56840738 ATGTCTCCAGCCAGGTGCGGTGGCTCACACCTATAATCCCAACATTTTGGGAGGCTGAGGCGGAC ATGTCTCCAGCCAGGTGCGGTGGCTCACACCTCTAATCCCAACATTTTGGGAGGCTGAGGCGGAC A C NUP93 Ensembl:ENSG00000102900 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1447644725 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_369307,RMVar_hsa_circ_178604,RMVar_hsa_circ_94937,RMVar_hsa_circ_178607,RMVar_hsa_circ_178608,RMVar_hsa_circ_178610,RMVar_hsa_circ_325460 37861 RMVar_ID_37861 Human_SNP_ID_604000631 A-to-I Human chr16 + 56877793 56877793 56877793 GTGGCCTCTGTGGCGCAGGCGTGGAGCTGTTGAATTTCTTCTCTCTGCCTCCATTTCCCAGGGCC GTGGCCTCTGTGGCGCAGGCGTGGAGCTGTTGCATTTCTTCTCTCTGCCTCCATTTCCCAGGGCC A C SLC12A3 Ensembl:ENSG00000070915 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1227320457 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22007,RMVar_hsa_circ_96542,RMVar_hsa_circ_178617,RMVar_hsa_circ_101616,RMVar_hsa_circ_178616,RMVar_hsa_circ_127714,RMVar_hsa_circ_178621,RMVar_hsa_circ_178622,RMVar_hsa_circ_119026,RMVar_hsa_circ_83019,RMVar_hsa_circ_85427,RMVar_hsa_circ_25096,RMVar_hsa_circ_178625,RMVar_hsa_circ_116974,RMVar_hsa_circ_178627,RMVar_hsa_circ_119258,RMVar_hsa_circ_117568,RMVar_hsa_circ_178628,RMVar_hsa_circ_112142,RMVar_hsa_circ_178630,RMVar_hsa_circ_178631,RMVar_hsa_circ_178632 37862 RMVar_ID_37862 Human_SNP_ID_604010032 A-to-I Human chr16 + 56910614 56910613 56910614 CACCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGTGCCTGGCCTCAAAAC CACCTGCCTTGGCCTCCCAAAGTGCTGGGATT_CAGGCATGAGCCACTGTGCCTGGCCTCAAAAC TA T SLC12A3 Ensembl:ENSG00000070915 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1258420130 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_127714,RMVar_hsa_circ_178621 37863 RMVar_ID_37863 Human_SNP_ID_604010241 A-to-I Human chr16 + 56911425 56911425 56911425 ATGCTCACTGCAGCCTCGACCTCCCAGGCTCAAACGATCCTCCCGCCTCAGCATCCTGAGGAGCT ATGCTCACTGCAGCCTCGACCTCCCAGGCTCAGACGATCCTCCCGCCTCAGCATCCTGAGGAGCT A G SLC12A3 Ensembl:ENSG00000070915 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1315845818 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127714,RMVar_hsa_circ_178621 37864 RMVar_ID_37864 Human_SNP_ID_604017833 A-to-I Human chr16 + 56940367 56940367 56940367 ATGGAGTCTCGCTCTGTCATTCAGGCTGGAGTACAATGGCACAATCACTGCAATCTCCGCTTCCC ATGGAGTCTCGCTCTGTCATTCAGGCTGGAGTGCAATGGCACAATCACTGCAATCTCCGCTTCCC A G HERPUD1,AC012181.2 Ensembl:ENSG00000051108,Ensembl:ENSG00000261270 Protein coding,lincRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1383159976 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_760063,Human_RBP_ID_893067,Human_RBP_ID_3511105,Human_RBP_ID_8188386 Human_Splice_Rec_1716569 RMVar_hsa_circ_5852,RMVar_hsa_circ_178646,RMVar_hsa_circ_317081,RMVar_hsa_circ_282835,RMVar_hsa_circ_178648,RMVar_hsa_circ_178650,RMVar_hsa_circ_361763 37865 RMVar_ID_37865 Human_SNP_ID_604017834 A-to-I Human chr16 + 56940369 56940369 56940369 GGAGTCTCGCTCTGTCATTCAGGCTGGAGTACAATGGCACAATCACTGCAATCTCCGCTTCCCAG GGAGTCTCGCTCTGTCATTCAGGCTGGAGTACGATGGCACAATCACTGCAATCTCCGCTTCCCAG A G HERPUD1,AC012181.2 Ensembl:ENSG00000051108,Ensembl:ENSG00000261270 Protein coding,lincRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348961371 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_760063,Human_RBP_ID_3511105,Human_RBP_ID_8188386 Human_Splice_Rec_1716569 RMVar_hsa_circ_5852,RMVar_hsa_circ_178646,RMVar_hsa_circ_317081,RMVar_hsa_circ_282835,RMVar_hsa_circ_178648,RMVar_hsa_circ_178650,RMVar_hsa_circ_361763 37866 RMVar_ID_37866 Human_SNP_ID_604017911 A-to-I Human chr16 + 56940700 56940700 56940700 ATATCACTCTGTGGCTGGGCGCAGTGGCTCACACCTGTAATCCCAGCAGTTTGGGAGGCCGAGGC ATATCACTCTGTGGCTGGGCGCAGTGGCTCACCCCTGTAATCCCAGCAGTTTGGGAGGCCGAGGC A C HERPUD1,AC012181.2 Ensembl:ENSG00000051108,Ensembl:ENSG00000261270 Protein coding,lincRNA intron,intron GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs530943383 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5852,RMVar_hsa_circ_178646,RMVar_hsa_circ_317081,RMVar_hsa_circ_282835,RMVar_hsa_circ_178648,RMVar_hsa_circ_178650,RMVar_hsa_circ_361763 37867 RMVar_ID_37867 Human_SNP_ID_604017949 A-to-I Human chr16 + 56940859 56940859 56940859 GTGGCACGGGCCTGTAATTTACTTGGGTGGCTAAGGCAGGAGAATTGCTTGAACTGGGGAGGCAG GTGGCACGGGCCTGTAATTTACTTGGGTGGCTCAGGCAGGAGAATTGCTTGAACTGGGGAGGCAG A C HERPUD1,AC012181.2 Ensembl:ENSG00000051108,Ensembl:ENSG00000261270 Protein coding,lincRNA intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs896501838 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5259721,Human_RBP_ID_17564187 RMVar_hsa_circ_5852,RMVar_hsa_circ_178646,RMVar_hsa_circ_317081,RMVar_hsa_circ_282835,RMVar_hsa_circ_178648,RMVar_hsa_circ_178650,RMVar_hsa_circ_361763 37868 RMVar_ID_37868 Human_SNP_ID_604017950 A-to-I Human chr16 + 56940859 56940859 56940859 GTGGCACGGGCCTGTAATTTACTTGGGTGGCTAAGGCAGGAGAATTGCTTGAACTGGGGAGGCAG GTGGCACGGGCCTGTAATTTACTTGGGTGGCTGAGGCAGGAGAATTGCTTGAACTGGGGAGGCAG A G HERPUD1,AC012181.2 Ensembl:ENSG00000051108,Ensembl:ENSG00000261270 Protein coding,lincRNA intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs896501838 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5259721,Human_RBP_ID_17564187 RMVar_hsa_circ_5852,RMVar_hsa_circ_178646,RMVar_hsa_circ_317081,RMVar_hsa_circ_282835,RMVar_hsa_circ_178648,RMVar_hsa_circ_178650,RMVar_hsa_circ_361763 37869 RMVar_ID_37869 Human_SNP_ID_604018182 A-to-I Human chr16 + 56941953 56941953 56941953 GCAATGATGAATAAAACACAGTCCCTGCCTTCAAGGACCTTACAGACTGGTGAGAATGTCTGGGA GCAATGATGAATAAAACACAGTCCCTGCCTTCGAGGACCTTACAGACTGGTGAGAATGTCTGGGA A G HERPUD1 Ensembl:ENSG00000051108 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs936677867 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1519521,Human_RBP_ID_12760295 RMVar_hsa_circ_5852,RMVar_hsa_circ_178646,RMVar_hsa_circ_317081,RMVar_hsa_circ_282835,RMVar_hsa_circ_178648,RMVar_hsa_circ_178650,RMVar_hsa_circ_361763 37870 RMVar_ID_37870 Human_SNP_ID_604034775 A-to-I Human chr16 + 57005385 57005385 57005385 CAAATCAAATCAATATGAACTTGGGGTCAGGCATGGTGGCTCACACCTGTAATCCCAACACTTGG CAAATCAAATCAATATGAACTTGGGGTCAGGCGTGGTGGCTCACACCTGTAATCCCAACACTTGG A G NLRC5 Ensembl:ENSG00000140853 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1231748671 Functional Loss SNV dbSNP153 33..33 33 - - - 37871 RMVar_ID_37871 Human_SNP_ID_604048505 A-to-I Human chr16 + 57056403 57056403 57056403 GCCTCCAACTCCTGGGCTCAAGCGATCCTCCCACCTCAGCCTCTGGAGTAGCTGGGACTACAGGC GCCTCCAACTCCTGGGCTCAAGCGATCCTCCCGCCTCAGCCTCTGGAGTAGCTGGGACTACAGGC A G NLRC5 Ensembl:ENSG00000140853 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1469280538 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_126759 RMVar_hsa_circ_119999,RMVar_hsa_circ_178651,RMVar_hsa_circ_127534,RMVar_hsa_circ_268842,RMVar_hsa_circ_111670,RMVar_hsa_circ_178655,RMVar_hsa_circ_178656,RMVar_hsa_circ_178658,RMVar_hsa_circ_370538 37872 RMVar_ID_37872 Human_SNP_ID_604048507 A-to-I Human chr16 + 57056408 57056408 57056408 CAACTCCTGGGCTCAAGCGATCCTCCCACCTCAGCCTCTGGAGTAGCTGGGACTACAGGCACACA CAACTCCTGGGCTCAAGCGATCCTCCCACCTCGGCCTCTGGAGTAGCTGGGACTACAGGCACACA A G NLRC5 Ensembl:ENSG00000140853 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs576798985 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_126759 RMVar_hsa_circ_119999,RMVar_hsa_circ_178651,RMVar_hsa_circ_127534,RMVar_hsa_circ_268842,RMVar_hsa_circ_111670,RMVar_hsa_circ_178655,RMVar_hsa_circ_178656,RMVar_hsa_circ_178658,RMVar_hsa_circ_370538 37873 RMVar_ID_37873 Human_SNP_ID_604048699 A-to-I Human chr16 + 57057287 57057287 57057287 TACTAAAAATACAAAAATAATTAGCCAGGCATAGTGGCACATGCCTGTAATCCCAGCTACTTGGG TACTAAAAATACAAAAATAATTAGCCAGGCATGGTGGCACATGCCTGTAATCCCAGCTACTTGGG A G NLRC5 Ensembl:ENSG00000140853 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs62037273 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119999,RMVar_hsa_circ_178651,RMVar_hsa_circ_127534,RMVar_hsa_circ_268842,RMVar_hsa_circ_111670,RMVar_hsa_circ_178655,RMVar_hsa_circ_178656,RMVar_hsa_circ_178658,RMVar_hsa_circ_370538 37874 RMVar_ID_37874 Human_SNP_ID_604050296 A-to-I Human chr16 + 57063199 57063199 57063199 CACTGGCTCGATCTCAGCTCACTGCACCCTCCACCTCTTGGGTTCAAGCGATTCTCCTGCCTCAG CACTGGCTCGATCTCAGCTCACTGCACCCTCCGCCTCTTGGGTTCAAGCGATTCTCCTGCCTCAG A G NLRC5 Ensembl:ENSG00000140853 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs565151498 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119999,RMVar_hsa_circ_178651,RMVar_hsa_circ_268842,RMVar_hsa_circ_178658,RMVar_hsa_circ_370538 37875 RMVar_ID_37875 Human_SNP_ID_604050348 A-to-I Human chr16 + 57063350 57063350 57063350 GTTGGCGAGGCTGGTCTCGAACTCCTGACCTCAGATGATCTGCCCGTTTCGGCCTTCCAAAGTGC GTTGGCGAGGCTGGTCTCGAACTCCTGACCTCGGATGATCTGCCCGTTTCGGCCTTCCAAAGTGC A G NLRC5 Ensembl:ENSG00000140853 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1165661783 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8435503 RMVar_hsa_circ_119999,RMVar_hsa_circ_178651,RMVar_hsa_circ_268842,RMVar_hsa_circ_178658,RMVar_hsa_circ_370538 37876 RMVar_ID_37876 Human_SNP_ID_604050557 A-to-I Human chr16 + 57064188 57064188 57064188 CAGGCGTTCAAGACCAGCCTGGACAACATGGCAAAACCCCATATCTACAAAAAATAAAAATAAAA CAGGCGTTCAAGACCAGCCTGGACAACATGGCGAAACCCCATATCTACAAAAAATAAAAATAAAA A G NLRC5 Ensembl:ENSG00000140853 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1245831756 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119999,RMVar_hsa_circ_178651,RMVar_hsa_circ_268842,RMVar_hsa_circ_178658,RMVar_hsa_circ_370538 37877 RMVar_ID_37877 Human_SNP_ID_604050558 A-to-I Human chr16 + 57064188 57064188 57064188 CAGGCGTTCAAGACCAGCCTGGACAACATGGCAAAACCCCATATCTACAAAAAATAAAAATAAAA CAGGCGTTCAAGACCAGCCTGGACAACATGGCTAAACCCCATATCTACAAAAAATAAAAATAAAA A T NLRC5 Ensembl:ENSG00000140853 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1245831756 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119999,RMVar_hsa_circ_178651,RMVar_hsa_circ_268842,RMVar_hsa_circ_178658,RMVar_hsa_circ_370538 37878 RMVar_ID_37878 Human_SNP_ID_604075915 A-to-I Human chr16 - 57168639 57168639 57168639 GCCACCACACCCAGCTAATTTTTTGTCTTTTTAGTAGAGACAGGGTTTCTCCATGCTGGTCAGGC GCCACCACACCCAGCTAATTTTTTGTCTTTTTTGTAGAGACAGGGTTTCTCCATGCTGGTCAGGC T A PSME3IP1 Ensembl:ENSG00000172775 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1435244803 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12760827 RMVar_hsa_circ_45649,RMVar_hsa_circ_178678,RMVar_hsa_circ_77293,RMVar_hsa_circ_280419,RMVar_hsa_circ_319864,RMVar_hsa_circ_54715,RMVar_hsa_circ_34406,RMVar_hsa_circ_326291,RMVar_hsa_circ_178680,RMVar_hsa_circ_67638,RMVar_hsa_circ_178681 37879 RMVar_ID_37879 Human_SNP_ID_604075916 A-to-I Human chr16 - 57168639 57168639 57168639 GCCACCACACCCAGCTAATTTTTTGTCTTTTTAGTAGAGACAGGGTTTCTCCATGCTGGTCAGGC GCCACCACACCCAGCTAATTTTTTGTCTTTTTGGTAGAGACAGGGTTTCTCCATGCTGGTCAGGC T C PSME3IP1 Ensembl:ENSG00000172775 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1435244803 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12760827 RMVar_hsa_circ_45649,RMVar_hsa_circ_178678,RMVar_hsa_circ_77293,RMVar_hsa_circ_280419,RMVar_hsa_circ_319864,RMVar_hsa_circ_54715,RMVar_hsa_circ_34406,RMVar_hsa_circ_326291,RMVar_hsa_circ_178680,RMVar_hsa_circ_67638,RMVar_hsa_circ_178681 37880 RMVar_ID_37880 Human_SNP_ID_604075936 A-to-I Human chr16 - 57168720 57168720 57168720 CAGCTCACCACAATCTCTGCCTCCCGGGTTCAAGCGATTCTCCTGGCTCAGCCTCCCGACTAGCT CAGCTCACCACAATCTCTGCCTCCCGGGTTCAGGCGATTCTCCTGGCTCAGCCTCCCGACTAGCT T C PSME3IP1 Ensembl:ENSG00000172775 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1040497422 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45649,RMVar_hsa_circ_178678,RMVar_hsa_circ_77293,RMVar_hsa_circ_280419,RMVar_hsa_circ_319864,RMVar_hsa_circ_54715,RMVar_hsa_circ_34406,RMVar_hsa_circ_326291,RMVar_hsa_circ_178680,RMVar_hsa_circ_67638,RMVar_hsa_circ_178681 37881 RMVar_ID_37881 Human_SNP_ID_604076314 A-to-I Human chr16 - 57170239 57170236 57170239 GTCTCTGCTAAAAATACAAAAATTAGCCGGGCATGGTGGCTTGTGCCTGTAGTCCCAACTACTCA GTCTCTGCTAAAAATACAAAAATTAGCCGGGC___GTGGCTTGTGCCTGTAGTCCCAACTACTCA CCAT C PSME3IP1 Ensembl:ENSG00000172775 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1185166946 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_45649,RMVar_hsa_circ_178678,RMVar_hsa_circ_77293,RMVar_hsa_circ_280419,RMVar_hsa_circ_319864,RMVar_hsa_circ_54715,RMVar_hsa_circ_34406,RMVar_hsa_circ_326291,RMVar_hsa_circ_178680,RMVar_hsa_circ_67638,RMVar_hsa_circ_178681 37882 RMVar_ID_37882 Human_SNP_ID_604076316 A-to-I Human chr16 - 57170239 57170239 57170239 GTCTCTGCTAAAAATACAAAAATTAGCCGGGCATGGTGGCTTGTGCCTGTAGTCCCAACTACTCA GTCTCTGCTAAAAATACAAAAATTAGCCGGGCTTGGTGGCTTGTGCCTGTAGTCCCAACTACTCA T A PSME3IP1 Ensembl:ENSG00000172775 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs188102518 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45649,RMVar_hsa_circ_178678,RMVar_hsa_circ_77293,RMVar_hsa_circ_280419,RMVar_hsa_circ_319864,RMVar_hsa_circ_54715,RMVar_hsa_circ_34406,RMVar_hsa_circ_326291,RMVar_hsa_circ_178680,RMVar_hsa_circ_67638,RMVar_hsa_circ_178681 37883 RMVar_ID_37883 Human_SNP_ID_604076439 A-to-I Human chr16 - 57170843 57170843 57170843 GTCTCGAACTCGTTACCTCAGGTGATCCGCCCACTCCAGCATCCCAAAGTGCAGGGATTACAGGC GTCTCGAACTCGTTACCTCAGGTGATCCGCCCCCTCCAGCATCCCAAAGTGCAGGGATTACAGGC T G PSME3IP1 Ensembl:ENSG00000172775 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1033630521 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45649,RMVar_hsa_circ_178678,RMVar_hsa_circ_77293,RMVar_hsa_circ_280419,RMVar_hsa_circ_319864,RMVar_hsa_circ_54715,RMVar_hsa_circ_34406,RMVar_hsa_circ_326291,RMVar_hsa_circ_178680,RMVar_hsa_circ_67638,RMVar_hsa_circ_178681 37884 RMVar_ID_37884 Human_SNP_ID_604076453 A-to-I Human chr16 - 57170900 57170900 57170900 CCCAGCTAATTCTTGTATTTTTAGTAGAGACGAGGTTTCATCATATTGGTCAGGCTGGTCTCGAA CCCAGCTAATTCTTGTATTTTTAGTAGAGACGGGGTTTCATCATATTGGTCAGGCTGGTCTCGAA T C PSME3IP1 Ensembl:ENSG00000172775 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1211277378 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45649,RMVar_hsa_circ_178678,RMVar_hsa_circ_77293,RMVar_hsa_circ_280419,RMVar_hsa_circ_319864,RMVar_hsa_circ_54715,RMVar_hsa_circ_34406,RMVar_hsa_circ_326291,RMVar_hsa_circ_178680,RMVar_hsa_circ_67638,RMVar_hsa_circ_178681 37885 RMVar_ID_37885 Human_SNP_ID_604076461 A-to-I Human chr16 - 57170929 57170929 57170929 AGCTGGGGTTACAGGTGCATGCCACCACGCCCAGCTAATTCTTGTATTTTTAGTAGAGACGAGGT AGCTGGGGTTACAGGTGCATGCCACCACGCCCGGCTAATTCTTGTATTTTTAGTAGAGACGAGGT T C PSME3IP1 Ensembl:ENSG00000172775 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1403459294 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45649,RMVar_hsa_circ_178678,RMVar_hsa_circ_77293,RMVar_hsa_circ_280419,RMVar_hsa_circ_319864,RMVar_hsa_circ_54715,RMVar_hsa_circ_34406,RMVar_hsa_circ_326291,RMVar_hsa_circ_178680,RMVar_hsa_circ_67638,RMVar_hsa_circ_178681 37886 RMVar_ID_37886 Human_SNP_ID_604077265 A-to-I Human chr16 - 57174033 57174033 57174033 CCTCGGCCTCCCAAAGTGCCAGGATTACAGGCATGAGCCACCGCACCCGGCCGAGAATTTTTTCA CCTCGGCCTCCCAAAGTGCCAGGATTACAGGCGTGAGCCACCGCACCCGGCCGAGAATTTTTTCA T C PSME3IP1 Ensembl:ENSG00000172775 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1331199956 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_178678,RMVar_hsa_circ_77293,RMVar_hsa_circ_54715,RMVar_hsa_circ_34406,RMVar_hsa_circ_67638 37887 RMVar_ID_37887 Human_SNP_ID_604077303 A-to-I Human chr16 - 57174182 57174182 57174182 TCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGTGCGTGCCACCGTGCCTG TCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTGGCTGGGATTACAGGTGCGTGCCACCGTGCCTG T C PSME3IP1 Ensembl:ENSG00000172775 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1423525043 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1717819,Human_Splice_Rec_1717855 RMVar_hsa_circ_178678,RMVar_hsa_circ_77293,RMVar_hsa_circ_54715,RMVar_hsa_circ_34406,RMVar_hsa_circ_67638 37888 RMVar_ID_37888 Human_SNP_ID_604077321 A-to-I Human chr16 - 57174267 57174267 57174267 TTTTTTGAGACAGAATCTTGCCCTGTCGCTCAAGCTGGGGTGCAGCGGTGTGATCTTGGCTCACT TTTTTTGAGACAGAATCTTGCCCTGTCGCTCACGCTGGGGTGCAGCGGTGTGATCTTGGCTCACT T G PSME3IP1 Ensembl:ENSG00000172775 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs888608982 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1717818,Human_Splice_Rec_1717819,Human_Splice_Rec_1717854,Human_Splice_Rec_1717855 RMVar_hsa_circ_178678,RMVar_hsa_circ_77293,RMVar_hsa_circ_54715,RMVar_hsa_circ_34406,RMVar_hsa_circ_67638 37889 RMVar_ID_37889 Human_SNP_ID_604077327 A-to-I Human chr16 - 57174285 57174285 57174285 TATTTGAGAGTTTTTTTTTTTTTTGAGACAGAATCTTGCCCTGTCGCTCAAGCTGGGGTGCAGCG TATTTGAGAGTTTTTTTTTTTTTTGAGACAGAGTCTTGCCCTGTCGCTCAAGCTGGGGTGCAGCG T C PSME3IP1 Ensembl:ENSG00000172775 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1376411905 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12876003 Human_Splice_Rec_1717818,Human_Splice_Rec_1717854 RMVar_hsa_circ_178678,RMVar_hsa_circ_77293,RMVar_hsa_circ_54715,RMVar_hsa_circ_34406,RMVar_hsa_circ_67638 37890 RMVar_ID_37890 Human_SNP_ID_604077508 A-to-I Human chr16 - 57175126 57175126 57175126 CCTGTAGTCCCAGCTAGTCAGGAGGCGGAGGCAGGAGAATCGCTTGAACCTGGGAGGCGGAGGTT CCTGTAGTCCCAGCTAGTCAGGAGGCGGAGGCGGGAGAATCGCTTGAACCTGGGAGGCGGAGGTT T C PSME3IP1 Ensembl:ENSG00000172775 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1226336244 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_178678,RMVar_hsa_circ_77293,RMVar_hsa_circ_54715,RMVar_hsa_circ_34406 37891 RMVar_ID_37891 Human_SNP_ID_604077865 A-to-I Human chr16 - 57176912 57176912 57176912 AAGCGGAGGTTGCAGTGAGCCAAGATCGTGCCACTGCACTCCGGCCTGGGCGGCAGAGCGAGACT AAGCGGAGGTTGCAGTGAGCCAAGATCGTGCCGCTGCACTCCGGCCTGGGCGGCAGAGCGAGACT T C PSME3IP1 Ensembl:ENSG00000172775 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1226663883 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25216571 RMVar_hsa_circ_178678,RMVar_hsa_circ_77293,RMVar_hsa_circ_54715,RMVar_hsa_circ_34406 37892 RMVar_ID_37892 Human_SNP_ID_604077884 A-to-I Human chr16 - 57176992 57176992 57176992 AAATTAGCCGGGCATGGTAGCACACACCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAA AAATTAGCCGGGCATGGTAGCACACACCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAA T C PSME3IP1 Ensembl:ENSG00000172775 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1244617300 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_178678,RMVar_hsa_circ_77293,RMVar_hsa_circ_54715,RMVar_hsa_circ_34406 37893 RMVar_ID_37893 Human_SNP_ID_604077889 A-to-I Human chr16 - 57177006 57177006 57177006 TACTAAAAATACAAAAATTAGCCGGGCATGGTAGCACACACCTGTAATCCCAGCTACTCAGGAGG TACTAAAAATACAAAAATTAGCCGGGCATGGTGGCACACACCTGTAATCCCAGCTACTCAGGAGG T C PSME3IP1 Ensembl:ENSG00000172775 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1261624935 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_178678,RMVar_hsa_circ_77293,RMVar_hsa_circ_54715,RMVar_hsa_circ_34406 37894 RMVar_ID_37894 Human_SNP_ID_604077902 A-to-I Human chr16 - 57177037 57177037 57177037 CAGCCTGGCCAACATAATGAAAGCCCATCTTTACTAAAAATACAAAAATTAGCCGGGCATGGTAG CAGCCTGGCCAACATAATGAAAGCCCATCTTTTCTAAAAATACAAAAATTAGCCGGGCATGGTAG T A PSME3IP1 Ensembl:ENSG00000172775 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1310987060 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_178678,RMVar_hsa_circ_77293,RMVar_hsa_circ_54715,RMVar_hsa_circ_34406 37895 RMVar_ID_37895 Human_SNP_ID_604077988 A-to-I Human chr16 - 57177346 57177346 57177346 CCTGTTTCACGAAAAAAAAAAAAAAAAAAATTAGCCAGGTGTAGTGGTGCATGCCTGTAGTCCCA CCTGTTTCACGAAAAAAAAAAAAAAAAAAATTTGCCAGGTGTAGTGGTGCATGCCTGTAGTCCCA T A PSME3IP1 Ensembl:ENSG00000172775 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs989348706 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_178678,RMVar_hsa_circ_77293,RMVar_hsa_circ_54715,RMVar_hsa_circ_34406 37896 RMVar_ID_37896 Human_SNP_ID_604078029 A-to-I Human chr16 - 57177467 57177467 57177467 AGATTGTAGGCCGGGCACAGTGGCTCATGCCTATAACCCCAGCACTTTGGCAGGCTGAGGTGGGC AGATTGTAGGCCGGGCACAGTGGCTCATGCCTGTAACCCCAGCACTTTGGCAGGCTGAGGTGGGC T C PSME3IP1 Ensembl:ENSG00000172775 Protein coding intron GSE47997;GSE38233;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;cultured B-cells;HepG2 cell line - 23474544,24183664,24183664,29129909 RNA-Seq:(High) rs1249304352 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_178678,RMVar_hsa_circ_77293,RMVar_hsa_circ_54715,RMVar_hsa_circ_34406 37897 RMVar_ID_37897 Human_SNP_ID_604078106 A-to-I Human chr16 - 57177749 57177749 57177749 CCTTGGCCTCCCAAAGTGTTGGGATTATAGGCATGAGCCACCATGCCCAGCCTGAATTAAGATAT CCTTGGCCTCCCAAAGTGTTGGGATTATAGGCGTGAGCCACCATGCCCAGCCTGAATTAAGATAT T C PSME3IP1 Ensembl:ENSG00000172775 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1490153172 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_178678,RMVar_hsa_circ_77293,RMVar_hsa_circ_54715,RMVar_hsa_circ_34406 37898 RMVar_ID_37898 Human_SNP_ID_604078126 A-to-I Human chr16 - 57177824 57177824 57177824 ACCATGCCTGGCTAGTTTTTTAAATTTTTTGTAGAGATGGGGGGTCTCACTTTGTTGCCCAGGCT ACCATGCCTGGCTAGTTTTTTAAATTTTTTGTTGAGATGGGGGGTCTCACTTTGTTGCCCAGGCT T A PSME3IP1 Ensembl:ENSG00000172775 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs767484438 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_178678,RMVar_hsa_circ_77293,RMVar_hsa_circ_54715,RMVar_hsa_circ_34406 37899 RMVar_ID_37899 Human_SNP_ID_604078134 A-to-I Human chr16 - 57177861 57177861 57177861 CTCAGCCTGTGAGTAGCTGGGACTACAGGCACACATCACCATGCCTGGCTAGTTTTTTAAATTTT CTCAGCCTGTGAGTAGCTGGGACTACAGGCACGCATCACCATGCCTGGCTAGTTTTTTAAATTTT T C PSME3IP1 Ensembl:ENSG00000172775 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs187300977 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23307630 RMVar_hsa_circ_178678,RMVar_hsa_circ_77293,RMVar_hsa_circ_54715,RMVar_hsa_circ_34406 37900 RMVar_ID_37900 Human_SNP_ID_604078142 A-to-I Human chr16 - 57177895 57177895 57177895 AGCCTTAGCCTCCTGGAGTAAATGATCCTCCCACCTCAGCCTGTGAGTAGCTGGGACTACAGGCA AGCCTTAGCCTCCTGGAGTAAATGATCCTCCCGCCTCAGCCTGTGAGTAGCTGGGACTACAGGCA T C PSME3IP1 Ensembl:ENSG00000172775 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs527867297 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_178678,RMVar_hsa_circ_77293,RMVar_hsa_circ_54715,RMVar_hsa_circ_34406 37901 RMVar_ID_37901 Human_SNP_ID_604079133 A-to-I Human chr16 - 57182502 57182502 57182502 CCTTATGTTGCCCGGGCTGGCCTTGAACTCCTAGGCTCAAGCAGTCCTCCAGTCTCAGCCTCCTG CCTTATGTTGCCCGGGCTGGCCTTGAACTCCTGGGCTCAAGCAGTCCTCCAGTCTCAGCCTCCTG T C PSME3IP1 Ensembl:ENSG00000172775 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1346058945 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_761985,Human_RBP_ID_12761218 RMVar_hsa_circ_178678,RMVar_hsa_circ_77293 37902 RMVar_ID_37902 Human_SNP_ID_604079241 A-to-I Human chr16 - 57182747 57182747 57182747 TGCTACTACGCCTGGCTAATTTTCATATTTTTAGTAGAGACGGAGTTTCACCATGTTGGTCAGGC TGCTACTACGCCTGGCTAATTTTCATATTTTTGGTAGAGACGGAGTTTCACCATGTTGGTCAGGC T C PSME3IP1 Ensembl:ENSG00000172775 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1163319662 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6522289 RMVar_hsa_circ_178678,RMVar_hsa_circ_77293 37903 RMVar_ID_37903 Human_SNP_ID_604079264 A-to-I Human chr16 - 57182827 57182827 57182827 CGGCTCACTACAACCTCCGCCTCCCGGGTTCAAGCAACTCTCCTTCCTCAGCCTCCCGAGTAGCT CGGCTCACTACAACCTCCGCCTCCCGGGTTCAGGCAACTCTCCTTCCTCAGCCTCCCGAGTAGCT T C PSME3IP1 Ensembl:ENSG00000172775 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1372586795 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_178678,RMVar_hsa_circ_77293 37904 RMVar_ID_37904 Human_SNP_ID_604079295 A-to-I Human chr16 - 57182924 57182924 57182924 ATAATAGGTTCTCGGTAAATATTTGCTTCAAAAATCTTTTTTCTTTGAGATGGAGTCTCGCCCAC ATAATAGGTTCTCGGTAAATATTTGCTTCAAATATCTTTTTTCTTTGAGATGGAGTCTCGCCCAC T A PSME3IP1 Ensembl:ENSG00000172775 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1318203124 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6522290,Human_RBP_ID_12761229 RMVar_hsa_circ_178678,RMVar_hsa_circ_77293 37905 RMVar_ID_37905 Human_SNP_ID_604079296 A-to-I Human chr16 - 57182924 57182924 57182924 ATAATAGGTTCTCGGTAAATATTTGCTTCAAAAATCTTTTTTCTTTGAGATGGAGTCTCGCCCAC ATAATAGGTTCTCGGTAAATATTTGCTTCAAACATCTTTTTTCTTTGAGATGGAGTCTCGCCCAC T G PSME3IP1 Ensembl:ENSG00000172775 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1318203124 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6522290,Human_RBP_ID_12761229 RMVar_hsa_circ_178678,RMVar_hsa_circ_77293 37906 RMVar_ID_37906 Human_SNP_ID_604079396 A-to-I Human chr16 - 57183405 57183405 57183405 TCGCTTGAACCTGGGAGGTGGAGGTTGCAATGAGCTGAGATCATGCCACTGCACTCTAGTCTGTG TCGCTTGAACCTGGGAGGTGGAGGTTGCAATGCGCTGAGATCATGCCACTGCACTCTAGTCTGTG T G PSME3IP1 Ensembl:ENSG00000172775 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1356040193 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_178678,RMVar_hsa_circ_77293 37907 RMVar_ID_37907 Human_SNP_ID_604079397 A-to-I Human chr16 - 57183408 57183408 57183408 GAATCGCTTGAACCTGGGAGGTGGAGGTTGCAATGAGCTGAGATCATGCCACTGCACTCTAGTCT GAATCGCTTGAACCTGGGAGGTGGAGGTTGCAGTGAGCTGAGATCATGCCACTGCACTCTAGTCT T C PSME3IP1 Ensembl:ENSG00000172775 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs756228984 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25216658 RMVar_hsa_circ_178678,RMVar_hsa_circ_77293 37908 RMVar_ID_37908 Human_SNP_ID_604079410 A-to-I Human chr16 - 57183438 57183437 57183438 ATCCCAGCTATTCGGGAGGCAGAGGTAGGAGAATCGCTTGAACCTGGGAGGTGGAGGTTGCAATG ATCCCAGCTATTCGGGAGGCAGAGGTAGGAGA_TCGCTTGAACCTGGGAGGTGGAGGTTGCAATG AT A PSME3IP1 Ensembl:ENSG00000172775 Protein coding intron GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs1342019944 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_178678,RMVar_hsa_circ_77293 37909 RMVar_ID_37909 Human_SNP_ID_604079413 A-to-I Human chr16 - 57183444 57183444 57183444 CCTGCAATCCCAGCTATTCGGGAGGCAGAGGTAGGAGAATCGCTTGAACCTGGGAGGTGGAGGTT CCTGCAATCCCAGCTATTCGGGAGGCAGAGGTGGGAGAATCGCTTGAACCTGGGAGGTGGAGGTT T C PSME3IP1 Ensembl:ENSG00000172775 Protein coding intron GSE47997;GSE38233;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,32596459 RNA-Seq:(High) rs1192271617 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_178678,RMVar_hsa_circ_77293 37910 RMVar_ID_37910 Human_SNP_ID_604079417 A-to-I Human chr16 - 57183470 57183470 57183470 AAATTAGCCAGTCATGGTGGCGGGCACCTGCAATCCCAGCTATTCGGGAGGCAGAGGTAGGAGAA AAATTAGCCAGTCATGGTGGCGGGCACCTGCAGTCCCAGCTATTCGGGAGGCAGAGGTAGGAGAA T C PSME3IP1 Ensembl:ENSG00000172775 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1342986112 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_178678,RMVar_hsa_circ_77293 37911 RMVar_ID_37911 Human_SNP_ID_604081798 A-to-I Human chr16 + 57192990 57192990 57192990 TGCCTGCCTTGGCCTCCCAGAGTGTTGGGATTACAGGTGTGAGCCACCATGCCCTGCTCAGATAG TGCCTGCCTTGGCCTCCCAGAGTGTTGGGATTGCAGGTGTGAGCCACCATGCCCTGCTCAGATAG A G RSPRY1 Ensembl:ENSG00000159579 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs148783556 Functional Loss SNV dbSNP153 33..33 33 - - - 37912 RMVar_ID_37912 Human_SNP_ID_604085585 A-to-I Human chr16 + 57206267 57206267 57206267 CTCTGCAAAAAAAATTTAAAAATTATCCAGGTACAGTGGCACTTGCCTGTGATCCCAGCTACTCA CTCTGCAAAAAAAATTTAAAAATTATCCAGGTGCAGTGGCACTTGCCTGTGATCCCAGCTACTCA A G RSPRY1 Ensembl:ENSG00000159579 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1345837507 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17565069 RMVar_hsa_circ_14462,RMVar_hsa_circ_347477,RMVar_hsa_circ_372792,RMVar_hsa_circ_275680,RMVar_hsa_circ_330545,RMVar_hsa_circ_14508,RMVar_hsa_circ_178683,RMVar_hsa_circ_178684,RMVar_hsa_circ_178685,RMVar_hsa_circ_178682 37913 RMVar_ID_37913 Human_SNP_ID_604085659 A-to-I Human chr16 + 57206594 57206594 57206594 GTTTTGTTTTGTTTTTAAAGAGACAGGGTCTCACTTTGTCACCCAGGCTGGCGTACAGTGGCGTG GTTTTGTTTTGTTTTTAAAGAGACAGGGTCTCCCTTTGTCACCCAGGCTGGCGTACAGTGGCGTG A C RSPRY1 Ensembl:ENSG00000159579 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1225594815 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17564190 RMVar_hsa_circ_14462,RMVar_hsa_circ_347477,RMVar_hsa_circ_372792,RMVar_hsa_circ_275680,RMVar_hsa_circ_330545,RMVar_hsa_circ_14508,RMVar_hsa_circ_178683,RMVar_hsa_circ_178684,RMVar_hsa_circ_178685,RMVar_hsa_circ_178682 37914 RMVar_ID_37914 Human_SNP_ID_604085701 A-to-I Human chr16 + 57206774 57206774 57206774 TTTTTGTAGAGCCAGGTCTTGCCATGTTGCCCAGGCTGGTCTCAAATACCTGGACTCAAGCGATT TTTTTGTAGAGCCAGGTCTTGCCATGTTGCCCGGGCTGGTCTCAAATACCTGGACTCAAGCGATT A G RSPRY1 Ensembl:ENSG00000159579 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs749897761 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23164592 RMVar_hsa_circ_14462,RMVar_hsa_circ_347477,RMVar_hsa_circ_372792,RMVar_hsa_circ_275680,RMVar_hsa_circ_330545,RMVar_hsa_circ_14508,RMVar_hsa_circ_178683,RMVar_hsa_circ_178684,RMVar_hsa_circ_178685,RMVar_hsa_circ_178682 37915 RMVar_ID_37915 Human_SNP_ID_604089463 A-to-I Human chr16 + 57222284 57222284 57222284 GTTTTCTGATTTTCTGCTTTGCTTTTAGAGACAGGTCTCACTGTGTTGCTCAGGCTGGCCTCAAA GTTTTCTGATTTTCTGCTTTGCTTTTAGAGACGGGTCTCACTGTGTTGCTCAGGCTGGCCTCAAA A G RSPRY1 Ensembl:ENSG00000159579 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1315082133 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_347477,RMVar_hsa_circ_21558,RMVar_hsa_circ_119932,RMVar_hsa_circ_178682,RMVar_hsa_circ_178687,RMVar_hsa_circ_95786,RMVar_hsa_circ_307840,RMVar_hsa_circ_22539,RMVar_hsa_circ_86926,RMVar_hsa_circ_178693,RMVar_hsa_circ_103954,RMVar_hsa_circ_178694,RMVar_hsa_circ_178695 37916 RMVar_ID_37916 Human_SNP_ID_604090685 A-to-I Human chr16 + 57228179 57228179 57228179 CCTGCGGTCCCGGCTACTTGGGAGGCTGAGGCAGGAGAATCAGTTGAACCCAGGAGGCAGAGGTT CCTGCGGTCCCGGCTACTTGGGAGGCTGAGGCGGGAGAATCAGTTGAACCCAGGAGGCAGAGGTT A G RSPRY1 Ensembl:ENSG00000159579 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941790677 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_347477,RMVar_hsa_circ_21558,RMVar_hsa_circ_119932,RMVar_hsa_circ_178682,RMVar_hsa_circ_178687,RMVar_hsa_circ_95786,RMVar_hsa_circ_22539,RMVar_hsa_circ_86926,RMVar_hsa_circ_178693,RMVar_hsa_circ_103954,RMVar_hsa_circ_178694,RMVar_hsa_circ_178695,RMVar_hsa_circ_22937 37917 RMVar_ID_37917 Human_SNP_ID_604092702 A-to-I Human chr16 + 57236978 57236978 57236978 CACAAGGCCAGGAGTTTGAGACCAGCCTGGCCAAGACAGTGAAACCCCGTCTCTACTACAAATAC CACAAGGCCAGGAGTTTGAGACCAGCCTGGCCTAGACAGTGAAACCCCGTCTCTACTACAAATAC A T RSPRY1 Ensembl:ENSG00000159579 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1255324297 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95786,RMVar_hsa_circ_178693,RMVar_hsa_circ_103954,RMVar_hsa_circ_178694 37918 RMVar_ID_37918 Human_SNP_ID_604092779 A-to-I Human chr16 + 57237273 57237273 57237273 TCATGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTTGGATTACAGGCGCATGCCACCAGGCCCA TCATGCAATTCTCCTGCCTCAGCCTCCCGAGTGGCTTGGATTACAGGCGCATGCCACCAGGCCCA A G RSPRY1 Ensembl:ENSG00000159579 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1231508874 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95786,RMVar_hsa_circ_178693,RMVar_hsa_circ_103954,RMVar_hsa_circ_178694 37919 RMVar_ID_37919 Human_SNP_ID_604092780 A-to-I Human chr16 + 57237273 57237273 57237273 TCATGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTTGGATTACAGGCGCATGCCACCAGGCCCA TCATGCAATTCTCCTGCCTCAGCCTCCCGAGTTGCTTGGATTACAGGCGCATGCCACCAGGCCCA A T RSPRY1 Ensembl:ENSG00000159579 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1231508874 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95786,RMVar_hsa_circ_178693,RMVar_hsa_circ_103954,RMVar_hsa_circ_178694 37920 RMVar_ID_37920 Human_SNP_ID_604092782 A-to-I Human chr16 + 57237283 57237283 57237283 CTCCTGCCTCAGCCTCCCGAGTAGCTTGGATTACAGGCGCATGCCACCAGGCCCAGCTAATTTTT CTCCTGCCTCAGCCTCCCGAGTAGCTTGGATTGCAGGCGCATGCCACCAGGCCCAGCTAATTTTT A G RSPRY1 Ensembl:ENSG00000159579 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1277327389 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95786,RMVar_hsa_circ_178693,RMVar_hsa_circ_103954,RMVar_hsa_circ_178694 37921 RMVar_ID_37921 Human_SNP_ID_604125806 A-to-I Human chr16 + 57364880 57364880 57364880 GCTGGAGTGCAGTGGCGTGATCTCGGCTCACTACAACCTCGACCTCCTGGGTTCAAGCGATTCTC GCTGGAGTGCAGTGGCGTGATCTCGGCTCACTCCAACCTCGACCTCCTGGGTTCAAGCGATTCTC A C CCL22 Ensembl:ENSG00000102962 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1433032501 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_178703,RMVar_hsa_circ_126516 37922 RMVar_ID_37922 Human_SNP_ID_604146222 A-to-I Human chr16 - 57442481 57442481 57442481 AATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCACGTCGCCCAGGCTGGTCTTGAACTCCTGG AATTTTTGTATTTTTAGTAGAGATGGGGTTTCCCCACGTCGCCCAGGCTGGTCTTGAACTCCTGG T G CIAPIN1 Ensembl:ENSG00000005194 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1475651004 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12762178 37923 RMVar_ID_37923 Human_SNP_ID_604146824 A-to-I Human chr16 - 57445251 57445251 57445251 CCACTTGCTTCAGCCTCCCAAAGTGTGGGATTACAGGTGTGAGTCACTGCACCCAGCCCAGTTAG CCACTTGCTTCAGCCTCCCAAAGTGTGGGATTGCAGGTGTGAGTCACTGCACCCAGCCCAGTTAG T C CIAPIN1 Ensembl:ENSG00000005194 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1164844270 Functional Loss SNV dbSNP153 33..33 33 - - - 37924 RMVar_ID_37924 Human_SNP_ID_604146833 A-to-I Human chr16 - 57445302 57445302 57445302 GGTTTTCTCCATGTTGGCCAGGCTGGTCTTGAACTCCTGACCTCAGGTGATCCACTTGCTTCAGC GGTTTTCTCCATGTTGGCCAGGCTGGTCTTGATCTCCTGACCTCAGGTGATCCACTTGCTTCAGC T A CIAPIN1 Ensembl:ENSG00000005194 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1291029368 Functional Loss SNV dbSNP153 33..33 33 - - - 37925 RMVar_ID_37925 Human_SNP_ID_604146842 A-to-I Human chr16 - 57445341 57445341 57445341 CACCATGCCCAGCTAATCTTTGTATTTTTAGTAGAGACGGGTTTTCTCCATGTTGGCCAGGCTGG CACCATGCCCAGCTAATCTTTGTATTTTTAGTTGAGACGGGTTTTCTCCATGTTGGCCAGGCTGG T A CIAPIN1 Ensembl:ENSG00000005194 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs757148102 Functional Loss SNV dbSNP153 33..33 33 - - - 37926 RMVar_ID_37926 Human_SNP_ID_604147837 A-to-I Human chr16 + 57448687 57448687 57448687 TGCCTGCCTCAGCCTCCCAAAGTGTTGGGATTACAGGTATGAGCCACCGCCTAGCCCCCTTTTGT TGCCTGCCTCAGCCTCCCAAAGTGTTGGGATTGCAGGTATGAGCCACCGCCTAGCCCCCTTTTGT A G COQ9 Ensembl:ENSG00000088682 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1203659220 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_178706,RMVar_hsa_circ_82461 37927 RMVar_ID_37927 Human_SNP_ID_604147838 A-to-I Human chr16 + 57448687 57448687 57448687 TGCCTGCCTCAGCCTCCCAAAGTGTTGGGATTACAGGTATGAGCCACCGCCTAGCCCCCTTTTGT TGCCTGCCTCAGCCTCCCAAAGTGTTGGGATTTCAGGTATGAGCCACCGCCTAGCCCCCTTTTGT A T COQ9 Ensembl:ENSG00000088682 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1203659220 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_178706,RMVar_hsa_circ_82461 37928 RMVar_ID_37928 Human_SNP_ID_604147842 A-to-I Human chr16 + 57448693 57448693 57448693 CCTCAGCCTCCCAAAGTGTTGGGATTACAGGTATGAGCCACCGCCTAGCCCCCTTTTGTTGTATT CCTCAGCCTCCCAAAGTGTTGGGATTACAGGTGTGAGCCACCGCCTAGCCCCCTTTTGTTGTATT A G COQ9 Ensembl:ENSG00000088682 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs760561964 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_178706,RMVar_hsa_circ_82461 37929 RMVar_ID_37929 Human_SNP_ID_604150266 A-to-I Human chr16 - 57458494 57458494 57458494 GAAGATGACCTAGATCCCACTTTGGCTTCTTGACGGACCTTCCTCATACCTTAGATGGGAATGAC GAAGATGACCTAGATCCCACTTTGGCTTCTTGGCGGACCTTCCTCATACCTTAGATGGGAATGAC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs376825541 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_113 37930 RMVar_ID_37930 Human_SNP_ID_604151424 A-to-I Human chr16 + 57462737 57462737 57462737 GCTGGTGGCCCCTGGGCGAGATGCCGTACGCCAACCAGCCTACCGTGCGGATCACGGAGCTCACT GCTGGTGGCCCCTGGGCGAGATGCCGTACGCCGACCAGCCTACCGTGCGGATCACGGAGCTCACT A G POLR2C,AC009052.1 Ensembl:ENSG00000102978,Ensembl:ENSG00000260345 Protein coding,lincRNA exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1274221986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_760788,Human_RBP_ID_1282553,Human_RBP_ID_1519684,Human_RBP_ID_4373948,Human_RBP_ID_5274743,Human_RBP_ID_5317574,Human_RBP_ID_8435633,Human_RBP_ID_9285046,Human_RBP_ID_12762588 Human_Splice_Rec_1718375,Human_Splice_Rec_1718383,Human_Splice_Rec_1718395,Human_Splice_Rec_1718403,Human_Splice_Rec_1718417,Human_Splice_Rec_1718427,Human_Splice_Rec_1718443 RMVar_hsa_circ_100437,RMVar_hsa_circ_121760,RMVar_hsa_circ_178710,RMVar_hsa_circ_178711 37931 RMVar_ID_37931 Human_SNP_ID_604151696 A-to-I Human chr16 + 57463417 57463417 57463417 TTTTCAACTTTTATTTTGGAGTCAAGGGGTACATTGGTGCAGGTTTGTTGCCTGGGTATAGTGCG TTTTCAACTTTTATTTTGGAGTCAAGGGGTACGTTGGTGCAGGTTTGTTGCCTGGGTATAGTGCG A G POLR2C Ensembl:ENSG00000102978 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs375921619 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121760,RMVar_hsa_circ_86005,RMVar_hsa_circ_178711,RMVar_hsa_circ_378554,RMVar_hsa_circ_178712 37932 RMVar_ID_37932 Human_SNP_ID_604167132 A-to-I Human chr16 - 57523045 57523045 57523045 CTCATGTGTCAGCCTCCCGAGTAGCTAGGACTACAGGCACACACCACCACGCCCAGCTAATTCTT CTCATGTGTCAGCCTCCCGAGTAGCTAGGACTGCAGGCACACACCACCACGCCCAGCTAATTCTT T C CCDC102A Ensembl:ENSG00000135736 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1337453048 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49103,RMVar_hsa_circ_305794 37933 RMVar_ID_37933 Human_SNP_ID_604180150 A-to-I Human chr16 + 57573203 57573203 57573203 CCTGTAATCCCAGGACTTTGGAAGGCCGAGGCAGGTGGATCAACTGAGGTCAGGAGTTCGAGATC CCTGTAATCCCAGGACTTTGGAAGGCCGAGGCCGGTGGATCAACTGAGGTCAGGAGTTCGAGATC A C ADGRG5 Ensembl:ENSG00000159618 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1367235998 Functional Loss SNV dbSNP153 33..33 33 - - - 37934 RMVar_ID_37934 Human_SNP_ID_604180180 A-to-I Human chr16 + 57573313 57573313 57573313 AAAATTAGCTGGGCGTGGTGTCAGGATTCTGTAGTTCCAGCTACTCAGGAGGCTGAGAGAGGAGA AAAATTAGCTGGGCGTGGTGTCAGGATTCTGTGGTTCCAGCTACTCAGGAGGCTGAGAGAGGAGA A G ADGRG5 Ensembl:ENSG00000159618 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1470614272 Functional Loss SNV dbSNP153 33..33 33 - - - 37935 RMVar_ID_37935 Human_SNP_ID_604180182 A-to-I Human chr16 + 57573336 57573336 57573336 GGATTCTGTAGTTCCAGCTACTCAGGAGGCTGAGAGAGGAGAATTGCTTGAACCTGGGAGGCGGA GGATTCTGTAGTTCCAGCTACTCAGGAGGCTGCGAGAGGAGAATTGCTTGAACCTGGGAGGCGGA A C ADGRG5 Ensembl:ENSG00000159618 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1180552686 Functional Loss SNV dbSNP153 33..33 33 - - - 37936 RMVar_ID_37936 Human_SNP_ID_604180357 A-to-I Human chr16 + 57573983 57573983 57573983 ACCTCAAGTGATTCGCCCACCTCGGCCTCCCAAAGTGCTGAGATTACAGGCATGAGCCACCGCGC ACCTCAAGTGATTCGCCCACCTCGGCCTCCCAGAGTGCTGAGATTACAGGCATGAGCCACCGCGC A G ADGRG5 Ensembl:ENSG00000159618 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs969551272 Functional Loss SNV dbSNP153 33..33 33 - - - 37937 RMVar_ID_37937 Human_SNP_ID_604180361 A-to-I Human chr16 + 57573996 57573996 57573996 CGCCCACCTCGGCCTCCCAAAGTGCTGAGATTACAGGCATGAGCCACCGCGCCTGGCCTCCATTT CGCCCACCTCGGCCTCCCAAAGTGCTGAGATTTCAGGCATGAGCCACCGCGCCTGGCCTCCATTT A T ADGRG5 Ensembl:ENSG00000159618 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1035253473 Functional Loss SNV dbSNP153 33..33 33 - - - 37938 RMVar_ID_37938 Human_SNP_ID_604188002 A-to-I Human chr16 + 57604561 57604561 57604561 CGCTGGCCTTGGCCTCCCCAAGTGCTGGGATTACAGGCATGAGCCACCATGCCCAGCCTCCGAAC CGCTGGCCTTGGCCTCCCCAAGTGCTGGGATTGCAGGCATGAGCCACCATGCCCAGCCTCCGAAC A G - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs993913064 Functional Loss SNV dbSNP153 33..33 33 - - - 37939 RMVar_ID_37939 Human_SNP_ID_604188006 A-to-I Human chr16 + 57604567 57604567 57604567 CCTTGGCCTCCCCAAGTGCTGGGATTACAGGCATGAGCCACCATGCCCAGCCTCCGAACATTTTA CCTTGGCCTCCCCAAGTGCTGGGATTACAGGCGTGAGCCACCATGCCCAGCCTCCGAACATTTTA A G - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1432842957 Functional Loss SNV dbSNP153 33..33 33 - - - 37940 RMVar_ID_37940 Human_SNP_ID_604234328 A-to-I Human chr16 - 57773619 57773619 57773619 TTTTAGACAGCCTCGCTCTGTCACCCTGGGGTACAGTGATGCTATCATAGCTTACTGCAGCTTCA TTTTAGACAGCCTCGCTCTGTCACCCTGGGGTGCAGTGATGCTATCATAGCTTACTGCAGCTTCA T C KIFC3 Ensembl:ENSG00000140859 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1039358992 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12876124 RMVar_hsa_circ_1967 37941 RMVar_ID_37941 Human_SNP_ID_604235921 A-to-I Human chr16 - 57780502 57780502 57780502 GCATATATATATATTTTTTTTCTTGAGAGAGAATCTTGCTCTGTCACCCAGGCTGGAGTGAAGTG GCATATATATATATTTTTTTTCTTGAGAGAGAGTCTTGCTCTGTCACCCAGGCTGGAGTGAAGTG T C KIFC3 Ensembl:ENSG00000140859 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs573586041 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1967 37942 RMVar_ID_37942 Human_SNP_ID_604236135 A-to-I Human chr16 - 57781205 57781205 57781205 GCTCAAGCCATCCTCCCACCTAAGCCTCCTGAATAACTAGGACCACAGGTGTCCACCACACCTGG GCTCAAGCCATCCTCCCACCTAAGCCTCCTGAGTAACTAGGACCACAGGTGTCCACCACACCTGG T C KIFC3 Ensembl:ENSG00000140859 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1555614430 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1967 37943 RMVar_ID_37943 Human_SNP_ID_604239591 A-to-I Human chr16 - 57794425 57794425 57794425 GCCCAGGAGTTCACGACCAGCCTGGACAATATAGTGAGACCCTATCTCTACAAAAAGAAAAATAA GCCCAGGAGTTCACGACCAGCCTGGACAATATGGTGAGACCCTATCTCTACAAAAAGAAAAATAA T C KIFC3 Ensembl:ENSG00000140859 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1442862060 Functional Loss SNV dbSNP153 33..33 33 - - - 37944 RMVar_ID_37944 Human_SNP_ID_604294210 A-to-I Human chr16 + 58003304 58003304 58003304 AAAAAATTAGCCAGGTGTGGTGGCACACGCCTATGGTTCCCACTACTTGAGAGGCTGAGGTAGGC AAAAAATTAGCCAGGTGTGGTGGCACACGCCTGTGGTTCCCACTACTTGAGAGGCTGAGGTAGGC A G USB1 Ensembl:ENSG00000103005 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs951109101 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121546,RMVar_hsa_circ_85931,RMVar_hsa_circ_178740,RMVar_hsa_circ_178742 37945 RMVar_ID_37945 Human_SNP_ID_604337533 A-to-I Human chr16 - 58169478 58169478 58169478 TTGCCCAGGCTGGAGTGCAGTGGCACCATCTCAGCTCACTGCAGCCTCCACCTCCCAGGTTCAAG TTGCCCAGGCTGGAGTGCAGTGGCACCATCTCGGCTCACTGCAGCCTCCACCTCCCAGGTTCAAG T C CSNK2A2 Ensembl:ENSG00000070770 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1185993438 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17901,RMVar_hsa_circ_365630,RMVar_hsa_circ_53743,RMVar_hsa_circ_3097,RMVar_hsa_circ_46417 37946 RMVar_ID_37946 Human_SNP_ID_604404278 A-to-I Human chr16 + 58441579 58441579 58441579 TTTTTTATTTTTTGTAAAGATGGGGTCTCCCTATGTTTCCCAGGCTGGTCTTGAACTCTTGGGCT TTTTTTATTTTTTGTAAAGATGGGGTCTCCCTGTGTTTCCCAGGCTGGTCTTGAACTCTTGGGCT A G LINC02137 Ensembl:ENSG00000260186 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569950205 Functional Loss SNV dbSNP153 33..33 33 - - - 37947 RMVar_ID_37947 Human_SNP_ID_604419578 A-to-I Human chr16 + 58501801 58501801 58501801 GGGGACAGGGGCGGCCACACCAGGGCTGGGAGAAGACAGTGGGGCCTCCTCAGCAGCAGAGAGCA GGGGACAGGGGCGGCCACACCAGGGCTGGGAGGAGACAGTGGGGCCTCCTCAGCAGCAGAGAGCA A G NDRG4 Ensembl:ENSG00000103034 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1181705630 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20750 37948 RMVar_ID_37948 Human_SNP_ID_604421071 A-to-I Human chr16 + 58505821 58505821 58505821 TCGGCCCACTGCAACCTCCACCTCCCTGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTAAGTAGC TCGGCCCACTGCAACCTCCACCTCCCTGGTTCTAGCAATTCTCCTGCCTCAGCCTCCTAAGTAGC A T NDRG4 Ensembl:ENSG00000103034 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs531159996 Functional Loss SNV dbSNP153 33..33 33 - - - 37949 RMVar_ID_37949 Human_SNP_ID_604426252 A-to-I Human chr16 - 58519625 58519625 58519625 TTTTTTTTTTTAAAGAAAATGAGTAGATACGTATTTAAAAACTTAACCCACTTAAAATTTGCCTT TTTTTTTTTTTAAAGAAAATGAGTAGATACGTGTTTAAAAACTTAACCCACTTAAAATTTGCCTT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs944466168 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25217304 37950 RMVar_ID_37950 Human_SNP_ID_604427994 A-to-I Human chr16 - 58525217 58525217 58525217 AATGAGCACCATCACTCACTCAGCACACATGGATATCTTCCAGAATTTGGCTGTGGACTTGGACA AATGAGCACCATCACTCACTCAGCACACATGGGTATCTTCCAGAATTTGGCTGTGGACTTGGACA T C CNOT1 Ensembl:ENSG00000125107 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs778870515 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1004931,Human_RBP_ID_1519932,Human_RBP_ID_1844104,Human_RBP_ID_3496982,Human_RBP_ID_4375056,Human_RBP_ID_8808598,Human_RBP_ID_9326012,Human_RBP_ID_12764891,Human_RBP_ID_17254799,Human_RBP_ID_17370258,Human_RBP_ID_17487046,Human_RBP_ID_18286291,Human_RBP_ID_18681261,Human_RBP_ID_22421779 Human_Splice_Rec_1721723,Human_Splice_Rec_1721739,Human_Splice_Rec_1721835,Human_Splice_Rec_1721933,Human_Splice_Rec_1721939 RMVar_hsa_circ_318,RMVar_hsa_circ_20288,RMVar_hsa_circ_78442,RMVar_hsa_circ_64447,RMVar_hsa_circ_178761,RMVar_hsa_circ_19105,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_327021,RMVar_hsa_circ_93605,RMVar_hsa_circ_178765,RMVar_hsa_circ_178767,RMVar_hsa_circ_82873,RMVar_hsa_circ_178766,RMVar_hsa_circ_178764 37951 RMVar_ID_37951 Human_SNP_ID_604438064 A-to-I Human chr16 - 58565259 58565259 58565259 AAACATTTAAAAATTAGCTGGGCATGGTCTGTATGCGTGGAGTCCCAGCAGCTGGGGAGGCTGAG AAACATTTAAAAATTAGCTGGGCATGGTCTGTGTGCGTGGAGTCCCAGCAGCTGGGGAGGCTGAG T C CNOT1 Ensembl:ENSG00000125107 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs969446232 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12766142,Human_RBP_ID_25217967 RMVar_hsa_circ_4429,RMVar_hsa_circ_84121,RMVar_hsa_circ_83986,RMVar_hsa_circ_119739,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_119415,RMVar_hsa_circ_178776,RMVar_hsa_circ_114456,RMVar_hsa_circ_178783,RMVar_hsa_circ_372807,RMVar_hsa_circ_361850,RMVar_hsa_circ_178786,RMVar_hsa_circ_128166,RMVar_hsa_circ_178790,RMVar_hsa_circ_88886,RMVar_hsa_circ_178791,RMVar_hsa_circ_376794,RMVar_hsa_circ_81146,RMVar_hsa_circ_103931,RMVar_hsa_circ_178796,RMVar_hsa_circ_178798,RMVar_hsa_circ_178802,RMVar_hsa_circ_51306,RMVar_hsa_circ_115468,RMVar_hsa_circ_178804,RMVar_hsa_circ_93835,RMVar_hsa_circ_178803,RMVar_hsa_circ_75924,RMVar_hsa_circ_107527,RMVar_hsa_circ_86057,RMVar_hsa_circ_178809,RMVar_hsa_circ_178810,RMVar_hsa_circ_178808,RMVar_hsa_circ_109818,RMVar_hsa_circ_178812,RMVar_hsa_circ_86089,RMVar_hsa_circ_178814,RMVar_hsa_circ_110381,RMVar_hsa_circ_73537,RMVar_hsa_circ_178817,RMVar_hsa_circ_356645,RMVar_hsa_circ_121420,RMVar_hsa_circ_178821,RMVar_hsa_circ_178823,RMVar_hsa_circ_51761,RMVar_hsa_circ_178822,RMVar_hsa_circ_60582,RMVar_hsa_circ_103073,RMVar_hsa_circ_51046,RMVar_hsa_circ_83523,RMVar_hsa_circ_178825,RMVar_hsa_circ_60317,RMVar_hsa_circ_112367,RMVar_hsa_circ_55810,RMVar_hsa_circ_57253,RMVar_hsa_circ_38766,RMVar_hsa_circ_178839,RMVar_hsa_circ_87340,RMVar_hsa_circ_97750,RMVar_hsa_circ_116657,RMVar_hsa_circ_178828,RMVar_hsa_circ_178830,RMVar_hsa_circ_178829,RMVar_hsa_circ_178827,RMVar_hsa_circ_360983,RMVar_hsa_circ_123305,RMVar_hsa_circ_114267,RMVar_hsa_circ_115165,RMVar_hsa_circ_108140,RMVar_hsa_circ_95481,RMVar_hsa_circ_96016,RMVar_hsa_circ_92019,RMVar_hsa_circ_79703,RMVar_hsa_circ_82762,RMVar_hsa_circ_84450,RMVar_hsa_circ_80784,RMVar_hsa_circ_178843,RMVar_hsa_circ_178847,RMVar_hsa_circ_178849,RMVar_hsa_circ_78836,RMVar_hsa_circ_178850,RMVar_hsa_circ_178848,RMVar_hsa_circ_178845,RMVar_hsa_circ_178846,RMVar_hsa_circ_178844,RMVar_hsa_circ_178841,RMVar_hsa_circ_178840,RMVar_hsa_circ_178835,RMVar_hsa_circ_178837,RMVar_hsa_circ_178838,RMVar_hsa_circ_178836,RMVar_hsa_circ_178834 37952 RMVar_ID_37952 Human_SNP_ID_604438818 A-to-I Human chr16 - 58568194 58568194 58568194 CCAGCTAATTTTGTATTTTCTTTAGTAGAGACAGGGTTTCTCATGTTGGGCAGGCTGGTCTCAAA CCAGCTAATTTTGTATTTTCTTTAGTAGAGACGGGGTTTCTCATGTTGGGCAGGCTGGTCTCAAA T C CNOT1 Ensembl:ENSG00000125107 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1034310424 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4429,RMVar_hsa_circ_84121,RMVar_hsa_circ_83986,RMVar_hsa_circ_119739,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_119415,RMVar_hsa_circ_178776,RMVar_hsa_circ_114456,RMVar_hsa_circ_178783,RMVar_hsa_circ_372807,RMVar_hsa_circ_361850,RMVar_hsa_circ_178786,RMVar_hsa_circ_128166,RMVar_hsa_circ_178790,RMVar_hsa_circ_88886,RMVar_hsa_circ_178791,RMVar_hsa_circ_376794,RMVar_hsa_circ_81146,RMVar_hsa_circ_103931,RMVar_hsa_circ_178796,RMVar_hsa_circ_178798,RMVar_hsa_circ_178802,RMVar_hsa_circ_51306,RMVar_hsa_circ_115468,RMVar_hsa_circ_178804,RMVar_hsa_circ_93835,RMVar_hsa_circ_178803,RMVar_hsa_circ_75924,RMVar_hsa_circ_107527,RMVar_hsa_circ_86057,RMVar_hsa_circ_178809,RMVar_hsa_circ_178810,RMVar_hsa_circ_178808,RMVar_hsa_circ_109818,RMVar_hsa_circ_178812,RMVar_hsa_circ_86089,RMVar_hsa_circ_178814,RMVar_hsa_circ_110381,RMVar_hsa_circ_73537,RMVar_hsa_circ_178817,RMVar_hsa_circ_356645,RMVar_hsa_circ_121420,RMVar_hsa_circ_178821,RMVar_hsa_circ_178823,RMVar_hsa_circ_51761,RMVar_hsa_circ_178822,RMVar_hsa_circ_60582,RMVar_hsa_circ_103073,RMVar_hsa_circ_51046,RMVar_hsa_circ_83523,RMVar_hsa_circ_178825,RMVar_hsa_circ_60317,RMVar_hsa_circ_112367,RMVar_hsa_circ_55810,RMVar_hsa_circ_57253,RMVar_hsa_circ_38766,RMVar_hsa_circ_178839,RMVar_hsa_circ_87340,RMVar_hsa_circ_97750,RMVar_hsa_circ_116657,RMVar_hsa_circ_178828,RMVar_hsa_circ_178830,RMVar_hsa_circ_178829,RMVar_hsa_circ_178827,RMVar_hsa_circ_360983,RMVar_hsa_circ_123305,RMVar_hsa_circ_114267,RMVar_hsa_circ_115165,RMVar_hsa_circ_108140,RMVar_hsa_circ_95481,RMVar_hsa_circ_96016,RMVar_hsa_circ_92019,RMVar_hsa_circ_79703,RMVar_hsa_circ_82762,RMVar_hsa_circ_84450,RMVar_hsa_circ_80784,RMVar_hsa_circ_178843,RMVar_hsa_circ_178847,RMVar_hsa_circ_178849,RMVar_hsa_circ_78836,RMVar_hsa_circ_178850,RMVar_hsa_circ_178848,RMVar_hsa_circ_178845,RMVar_hsa_circ_178846,RMVar_hsa_circ_178844,RMVar_hsa_circ_178841,RMVar_hsa_circ_178840,RMVar_hsa_circ_178835,RMVar_hsa_circ_178837,RMVar_hsa_circ_178838,RMVar_hsa_circ_178836,RMVar_hsa_circ_178834 37953 RMVar_ID_37953 Human_SNP_ID_604439097 A-to-I Human chr16 - 58569263 58569263 58569263 CAAAAATTAGCCAGGCATAGTGAAGGGCGACTATAGTCCCAGCTACTTGGGAGGCTGAGGCAAGA CAAAAATTAGCCAGGCATAGTGAAGGGCGACTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAAGA T C CNOT1 Ensembl:ENSG00000125107 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs773775246 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25245351 RMVar_hsa_circ_4429,RMVar_hsa_circ_84121,RMVar_hsa_circ_83986,RMVar_hsa_circ_119739,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_119415,RMVar_hsa_circ_178776,RMVar_hsa_circ_114456,RMVar_hsa_circ_178783,RMVar_hsa_circ_372807,RMVar_hsa_circ_361850,RMVar_hsa_circ_178786,RMVar_hsa_circ_128166,RMVar_hsa_circ_178790,RMVar_hsa_circ_88886,RMVar_hsa_circ_178791,RMVar_hsa_circ_376794,RMVar_hsa_circ_81146,RMVar_hsa_circ_103931,RMVar_hsa_circ_178796,RMVar_hsa_circ_178798,RMVar_hsa_circ_178802,RMVar_hsa_circ_51306,RMVar_hsa_circ_115468,RMVar_hsa_circ_178804,RMVar_hsa_circ_93835,RMVar_hsa_circ_178803,RMVar_hsa_circ_75924,RMVar_hsa_circ_107527,RMVar_hsa_circ_86057,RMVar_hsa_circ_178809,RMVar_hsa_circ_178810,RMVar_hsa_circ_178808,RMVar_hsa_circ_109818,RMVar_hsa_circ_178812,RMVar_hsa_circ_86089,RMVar_hsa_circ_178814,RMVar_hsa_circ_110381,RMVar_hsa_circ_73537,RMVar_hsa_circ_178817,RMVar_hsa_circ_356645,RMVar_hsa_circ_121420,RMVar_hsa_circ_178821,RMVar_hsa_circ_178823,RMVar_hsa_circ_51761,RMVar_hsa_circ_178822,RMVar_hsa_circ_60582,RMVar_hsa_circ_103073,RMVar_hsa_circ_51046,RMVar_hsa_circ_83523,RMVar_hsa_circ_178825,RMVar_hsa_circ_60317,RMVar_hsa_circ_112367,RMVar_hsa_circ_55810,RMVar_hsa_circ_57253,RMVar_hsa_circ_38766,RMVar_hsa_circ_178839,RMVar_hsa_circ_87340,RMVar_hsa_circ_97750,RMVar_hsa_circ_116657,RMVar_hsa_circ_178828,RMVar_hsa_circ_178830,RMVar_hsa_circ_178829,RMVar_hsa_circ_178827,RMVar_hsa_circ_360983,RMVar_hsa_circ_123305,RMVar_hsa_circ_114267,RMVar_hsa_circ_115165,RMVar_hsa_circ_108140,RMVar_hsa_circ_95481,RMVar_hsa_circ_96016,RMVar_hsa_circ_92019,RMVar_hsa_circ_79703,RMVar_hsa_circ_82762,RMVar_hsa_circ_84450,RMVar_hsa_circ_80784,RMVar_hsa_circ_178843,RMVar_hsa_circ_178847,RMVar_hsa_circ_178849,RMVar_hsa_circ_78836,RMVar_hsa_circ_178850,RMVar_hsa_circ_178848,RMVar_hsa_circ_178845,RMVar_hsa_circ_178846,RMVar_hsa_circ_178844,RMVar_hsa_circ_178841,RMVar_hsa_circ_178840,RMVar_hsa_circ_178835,RMVar_hsa_circ_178837,RMVar_hsa_circ_178838,RMVar_hsa_circ_178836,RMVar_hsa_circ_178834 37954 RMVar_ID_37954 Human_SNP_ID_604439098 A-to-I Human chr16 - 58569263 58569263 58569263 CAAAAATTAGCCAGGCATAGTGAAGGGCGACTATAGTCCCAGCTACTTGGGAGGCTGAGGCAAGA CAAAAATTAGCCAGGCATAGTGAAGGGCGACTCTAGTCCCAGCTACTTGGGAGGCTGAGGCAAGA T G CNOT1 Ensembl:ENSG00000125107 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs773775246 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25245351 RMVar_hsa_circ_4429,RMVar_hsa_circ_84121,RMVar_hsa_circ_83986,RMVar_hsa_circ_119739,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_119415,RMVar_hsa_circ_178776,RMVar_hsa_circ_114456,RMVar_hsa_circ_178783,RMVar_hsa_circ_372807,RMVar_hsa_circ_361850,RMVar_hsa_circ_178786,RMVar_hsa_circ_128166,RMVar_hsa_circ_178790,RMVar_hsa_circ_88886,RMVar_hsa_circ_178791,RMVar_hsa_circ_376794,RMVar_hsa_circ_81146,RMVar_hsa_circ_103931,RMVar_hsa_circ_178796,RMVar_hsa_circ_178798,RMVar_hsa_circ_178802,RMVar_hsa_circ_51306,RMVar_hsa_circ_115468,RMVar_hsa_circ_178804,RMVar_hsa_circ_93835,RMVar_hsa_circ_178803,RMVar_hsa_circ_75924,RMVar_hsa_circ_107527,RMVar_hsa_circ_86057,RMVar_hsa_circ_178809,RMVar_hsa_circ_178810,RMVar_hsa_circ_178808,RMVar_hsa_circ_109818,RMVar_hsa_circ_178812,RMVar_hsa_circ_86089,RMVar_hsa_circ_178814,RMVar_hsa_circ_110381,RMVar_hsa_circ_73537,RMVar_hsa_circ_178817,RMVar_hsa_circ_356645,RMVar_hsa_circ_121420,RMVar_hsa_circ_178821,RMVar_hsa_circ_178823,RMVar_hsa_circ_51761,RMVar_hsa_circ_178822,RMVar_hsa_circ_60582,RMVar_hsa_circ_103073,RMVar_hsa_circ_51046,RMVar_hsa_circ_83523,RMVar_hsa_circ_178825,RMVar_hsa_circ_60317,RMVar_hsa_circ_112367,RMVar_hsa_circ_55810,RMVar_hsa_circ_57253,RMVar_hsa_circ_38766,RMVar_hsa_circ_178839,RMVar_hsa_circ_87340,RMVar_hsa_circ_97750,RMVar_hsa_circ_116657,RMVar_hsa_circ_178828,RMVar_hsa_circ_178830,RMVar_hsa_circ_178829,RMVar_hsa_circ_178827,RMVar_hsa_circ_360983,RMVar_hsa_circ_123305,RMVar_hsa_circ_114267,RMVar_hsa_circ_115165,RMVar_hsa_circ_108140,RMVar_hsa_circ_95481,RMVar_hsa_circ_96016,RMVar_hsa_circ_92019,RMVar_hsa_circ_79703,RMVar_hsa_circ_82762,RMVar_hsa_circ_84450,RMVar_hsa_circ_80784,RMVar_hsa_circ_178843,RMVar_hsa_circ_178847,RMVar_hsa_circ_178849,RMVar_hsa_circ_78836,RMVar_hsa_circ_178850,RMVar_hsa_circ_178848,RMVar_hsa_circ_178845,RMVar_hsa_circ_178846,RMVar_hsa_circ_178844,RMVar_hsa_circ_178841,RMVar_hsa_circ_178840,RMVar_hsa_circ_178835,RMVar_hsa_circ_178837,RMVar_hsa_circ_178838,RMVar_hsa_circ_178836,RMVar_hsa_circ_178834 37955 RMVar_ID_37955 Human_SNP_ID_604439170 A-to-I Human chr16 - 58569560 58569560 58569560 CTTTTTCTGTTTGGTATGTTGTAGAGTGTAGTATCTGATGGGAAAAAACGAATTTCTGTTTTTTG CTTTTTCTGTTTGGTATGTTGTAGAGTGTAGTTTCTGATGGGAAAAAACGAATTTCTGTTTTTTG T A CNOT1 Ensembl:ENSG00000125107 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7192054 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1089706,Human_RBP_ID_6523877,Human_RBP_ID_12766305,Human_RBP_ID_23694414,Human_RBP_ID_27659439 GWAS_ID_4327,GWAS_ID_4328 RMVar_hsa_circ_4429,RMVar_hsa_circ_84121,RMVar_hsa_circ_83986,RMVar_hsa_circ_119739,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_119415,RMVar_hsa_circ_178776,RMVar_hsa_circ_114456,RMVar_hsa_circ_178783,RMVar_hsa_circ_372807,RMVar_hsa_circ_361850,RMVar_hsa_circ_178786,RMVar_hsa_circ_128166,RMVar_hsa_circ_178790,RMVar_hsa_circ_88886,RMVar_hsa_circ_178791,RMVar_hsa_circ_376794,RMVar_hsa_circ_81146,RMVar_hsa_circ_103931,RMVar_hsa_circ_178796,RMVar_hsa_circ_178798,RMVar_hsa_circ_178802,RMVar_hsa_circ_51306,RMVar_hsa_circ_115468,RMVar_hsa_circ_178804,RMVar_hsa_circ_93835,RMVar_hsa_circ_178803,RMVar_hsa_circ_75924,RMVar_hsa_circ_107527,RMVar_hsa_circ_86057,RMVar_hsa_circ_178809,RMVar_hsa_circ_178810,RMVar_hsa_circ_178808,RMVar_hsa_circ_109818,RMVar_hsa_circ_178812,RMVar_hsa_circ_86089,RMVar_hsa_circ_178814,RMVar_hsa_circ_110381,RMVar_hsa_circ_73537,RMVar_hsa_circ_178817,RMVar_hsa_circ_356645,RMVar_hsa_circ_121420,RMVar_hsa_circ_178821,RMVar_hsa_circ_178823,RMVar_hsa_circ_51761,RMVar_hsa_circ_178822,RMVar_hsa_circ_60582,RMVar_hsa_circ_103073,RMVar_hsa_circ_51046,RMVar_hsa_circ_83523,RMVar_hsa_circ_178825,RMVar_hsa_circ_60317,RMVar_hsa_circ_112367,RMVar_hsa_circ_55810,RMVar_hsa_circ_57253,RMVar_hsa_circ_38766,RMVar_hsa_circ_178839,RMVar_hsa_circ_87340,RMVar_hsa_circ_97750,RMVar_hsa_circ_116657,RMVar_hsa_circ_178828,RMVar_hsa_circ_178830,RMVar_hsa_circ_178829,RMVar_hsa_circ_178827,RMVar_hsa_circ_360983,RMVar_hsa_circ_123305,RMVar_hsa_circ_114267,RMVar_hsa_circ_115165,RMVar_hsa_circ_108140,RMVar_hsa_circ_95481,RMVar_hsa_circ_96016,RMVar_hsa_circ_92019,RMVar_hsa_circ_79703,RMVar_hsa_circ_82762,RMVar_hsa_circ_84450,RMVar_hsa_circ_80784,RMVar_hsa_circ_178843,RMVar_hsa_circ_178847,RMVar_hsa_circ_178849,RMVar_hsa_circ_78836,RMVar_hsa_circ_178850,RMVar_hsa_circ_178848,RMVar_hsa_circ_178845,RMVar_hsa_circ_178846,RMVar_hsa_circ_178844,RMVar_hsa_circ_178841,RMVar_hsa_circ_178840,RMVar_hsa_circ_178835,RMVar_hsa_circ_178837,RMVar_hsa_circ_178838,RMVar_hsa_circ_178836,RMVar_hsa_circ_178834 37956 RMVar_ID_37956 Human_SNP_ID_604439171 A-to-I Human chr16 - 58569560 58569560 58569560 CTTTTTCTGTTTGGTATGTTGTAGAGTGTAGTATCTGATGGGAAAAAACGAATTTCTGTTTTTTG CTTTTTCTGTTTGGTATGTTGTAGAGTGTAGTGTCTGATGGGAAAAAACGAATTTCTGTTTTTTG T C CNOT1 Ensembl:ENSG00000125107 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7192054 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1089706,Human_RBP_ID_6523877,Human_RBP_ID_12766305,Human_RBP_ID_23694414,Human_RBP_ID_27659439 GWAS_ID_4327,GWAS_ID_4328 RMVar_hsa_circ_4429,RMVar_hsa_circ_84121,RMVar_hsa_circ_83986,RMVar_hsa_circ_119739,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_119415,RMVar_hsa_circ_178776,RMVar_hsa_circ_114456,RMVar_hsa_circ_178783,RMVar_hsa_circ_372807,RMVar_hsa_circ_361850,RMVar_hsa_circ_178786,RMVar_hsa_circ_128166,RMVar_hsa_circ_178790,RMVar_hsa_circ_88886,RMVar_hsa_circ_178791,RMVar_hsa_circ_376794,RMVar_hsa_circ_81146,RMVar_hsa_circ_103931,RMVar_hsa_circ_178796,RMVar_hsa_circ_178798,RMVar_hsa_circ_178802,RMVar_hsa_circ_51306,RMVar_hsa_circ_115468,RMVar_hsa_circ_178804,RMVar_hsa_circ_93835,RMVar_hsa_circ_178803,RMVar_hsa_circ_75924,RMVar_hsa_circ_107527,RMVar_hsa_circ_86057,RMVar_hsa_circ_178809,RMVar_hsa_circ_178810,RMVar_hsa_circ_178808,RMVar_hsa_circ_109818,RMVar_hsa_circ_178812,RMVar_hsa_circ_86089,RMVar_hsa_circ_178814,RMVar_hsa_circ_110381,RMVar_hsa_circ_73537,RMVar_hsa_circ_178817,RMVar_hsa_circ_356645,RMVar_hsa_circ_121420,RMVar_hsa_circ_178821,RMVar_hsa_circ_178823,RMVar_hsa_circ_51761,RMVar_hsa_circ_178822,RMVar_hsa_circ_60582,RMVar_hsa_circ_103073,RMVar_hsa_circ_51046,RMVar_hsa_circ_83523,RMVar_hsa_circ_178825,RMVar_hsa_circ_60317,RMVar_hsa_circ_112367,RMVar_hsa_circ_55810,RMVar_hsa_circ_57253,RMVar_hsa_circ_38766,RMVar_hsa_circ_178839,RMVar_hsa_circ_87340,RMVar_hsa_circ_97750,RMVar_hsa_circ_116657,RMVar_hsa_circ_178828,RMVar_hsa_circ_178830,RMVar_hsa_circ_178829,RMVar_hsa_circ_178827,RMVar_hsa_circ_360983,RMVar_hsa_circ_123305,RMVar_hsa_circ_114267,RMVar_hsa_circ_115165,RMVar_hsa_circ_108140,RMVar_hsa_circ_95481,RMVar_hsa_circ_96016,RMVar_hsa_circ_92019,RMVar_hsa_circ_79703,RMVar_hsa_circ_82762,RMVar_hsa_circ_84450,RMVar_hsa_circ_80784,RMVar_hsa_circ_178843,RMVar_hsa_circ_178847,RMVar_hsa_circ_178849,RMVar_hsa_circ_78836,RMVar_hsa_circ_178850,RMVar_hsa_circ_178848,RMVar_hsa_circ_178845,RMVar_hsa_circ_178846,RMVar_hsa_circ_178844,RMVar_hsa_circ_178841,RMVar_hsa_circ_178840,RMVar_hsa_circ_178835,RMVar_hsa_circ_178837,RMVar_hsa_circ_178838,RMVar_hsa_circ_178836,RMVar_hsa_circ_178834 37957 RMVar_ID_37957 Human_SNP_ID_604447759 A-to-I Human chr16 - 58600179 58600179 58600179 CATGCCTGGCCAAATTTTTTTGTATTCTGAGTAGAGACGGGGTTTCACCATGTTGGCCAGACTGG CATGCCTGGCCAAATTTTTTTGTATTCTGAGTTGAGACGGGGTTTCACCATGTTGGCCAGACTGG T A CNOT1 Ensembl:ENSG00000125107 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1379363877 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12767306 RMVar_hsa_circ_88886,RMVar_hsa_circ_178791,RMVar_hsa_circ_84450,RMVar_hsa_circ_178834 37958 RMVar_ID_37958 Human_SNP_ID_604447760 A-to-I Human chr16 - 58600179 58600179 58600179 CATGCCTGGCCAAATTTTTTTGTATTCTGAGTAGAGACGGGGTTTCACCATGTTGGCCAGACTGG CATGCCTGGCCAAATTTTTTTGTATTCTGAGTGGAGACGGGGTTTCACCATGTTGGCCAGACTGG T C CNOT1 Ensembl:ENSG00000125107 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1379363877 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12767306 RMVar_hsa_circ_88886,RMVar_hsa_circ_178791,RMVar_hsa_circ_84450,RMVar_hsa_circ_178834 37959 RMVar_ID_37959 Human_SNP_ID_604449440 A-to-I Human chr16 - 58605500 58605499 58605501 TTATGTGTTTTTATTTTATTTTATTTTGAGACAGAGTCTTGCTCTGTCGCCTAGGCTGGAGTGCA TTATGTGTTTTTATTTTATTTTATTTTGAGA__GAGTCTTGCTCTGTCGCCTAGGCTGGAGTGCA CTG C CNOT1 Ensembl:ENSG00000125107 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs912636968 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_88886,RMVar_hsa_circ_178791,RMVar_hsa_circ_84450,RMVar_hsa_circ_178834 37960 RMVar_ID_37960 Human_SNP_ID_604451090 A-to-I Human chr16 - 58611393 58611393 58611393 ATGGAGTCTCGCTCTGTCGCTCAGACTGGAGTACAGTGGCGTGGTCTCGGCTCCCTGTAACCTCT ATGGAGTCTCGCTCTGTCGCTCAGACTGGAGTGCAGTGGCGTGGTCTCGGCTCCCTGTAACCTCT T C CNOT1 Ensembl:ENSG00000125107 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223894333 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12767629 RMVar_hsa_circ_88886,RMVar_hsa_circ_178791,RMVar_hsa_circ_84450,RMVar_hsa_circ_178834 37961 RMVar_ID_37961 Human_SNP_ID_604451267 A-to-I Human chr16 - 58612019 58612019 58612019 TGAGGTTGGCCGCGAGGTGTGGTCACACCACTAGACTCCAGCCTGGATAACAGAGCAAGACCCCT TGAGGTTGGCCGCGAGGTGTGGTCACACCACTGGACTCCAGCCTGGATAACAGAGCAAGACCCCT T C CNOT1 Ensembl:ENSG00000125107 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1277114270 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12767655 RMVar_hsa_circ_88886,RMVar_hsa_circ_178791,RMVar_hsa_circ_84450,RMVar_hsa_circ_178834 37962 RMVar_ID_37962 Human_SNP_ID_604451563 A-to-I Human chr16 - 58613196 58613196 58613196 AACCCCATCTCTACTAAAAATAAAAAAAAATTAGCTGGGCGTGTTGGCGCATGCCTGTAATCCCA AACCCCATCTCTACTAAAAATAAAAAAAAATTTGCTGGGCGTGTTGGCGCATGCCTGTAATCCCA T A CNOT1 Ensembl:ENSG00000125107 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1030554499 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88886,RMVar_hsa_circ_178791,RMVar_hsa_circ_84450,RMVar_hsa_circ_178834 37963 RMVar_ID_37963 Human_SNP_ID_604453021 A-to-I Human chr16 - 58619157 58619157 58619157 GGTCTCTGTTGCCCAGGCTGGAGTGCAGTGGCACGATCATGGCTCACTGCAACCATGACCTCCTG GGTCTCTGTTGCCCAGGCTGGAGTGCAGTGGCTCGATCATGGCTCACTGCAACCATGACCTCCTG T A CNOT1 Ensembl:ENSG00000125107 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1198124956 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88886,RMVar_hsa_circ_178791,RMVar_hsa_circ_84450,RMVar_hsa_circ_178834 37964 RMVar_ID_37964 Human_SNP_ID_604453625 A-to-I Human chr16 - 58621160 58621160 58621160 CCGAGGAGTTTCAGACCACCCTGGGCAATATGATGAAACCCCATCTCTGCTAAAAATACAAAACT CCGAGGAGTTTCAGACCACCCTGGGCAATATGGTGAAACCCCATCTCTGCTAAAAATACAAAACT T C CNOT1 Ensembl:ENSG00000125107 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs546456664 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17564204 RMVar_hsa_circ_88886,RMVar_hsa_circ_178791,RMVar_hsa_circ_84450,RMVar_hsa_circ_178834 37965 RMVar_ID_37965 Human_SNP_ID_604453680 A-to-I Human chr16 - 58621346 58621346 58621346 TCGCTGGACCCTGGGAGGTGGAGGTTGCGGTGAGCCGAGATTGCACCATTGCACTCCAGCCTAGG TCGCTGGACCCTGGGAGGTGGAGGTTGCGGTGTGCCGAGATTGCACCATTGCACTCCAGCCTAGG T A CNOT1 Ensembl:ENSG00000125107 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs139263225 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22715356 RMVar_hsa_circ_88886,RMVar_hsa_circ_178791,RMVar_hsa_circ_84450,RMVar_hsa_circ_178834 37966 RMVar_ID_37966 Human_SNP_ID_604453698 A-to-I Human chr16 - 58621402 58621402 58621402 GGGCGTGGTGGCGCGTGCCTGTAATCTCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTGGAC GGGCGTGGTGGCGCGTGCCTGTAATCTCAGCTGCTTGGGAGGCTGAGGCAGGAGAATCGCTGGAC T C CNOT1 Ensembl:ENSG00000125107 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs753158810 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88886,RMVar_hsa_circ_178791,RMVar_hsa_circ_84450,RMVar_hsa_circ_178834 37967 RMVar_ID_37967 Human_SNP_ID_604453718 A-to-I Human chr16 - 58621467 58621467 58621467 GGAGTTTGAGACCAGCTTGACCAACATGGAGAAACCCCGTATCCACTGAAAATACAAAATTAGTT GGAGTTTGAGACCAGCTTGACCAACATGGAGAGACCCCGTATCCACTGAAAATACAAAATTAGTT T C CNOT1 Ensembl:ENSG00000125107 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs957200408 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88886,RMVar_hsa_circ_178791,RMVar_hsa_circ_84450,RMVar_hsa_circ_178834 37968 RMVar_ID_37968 Human_SNP_ID_604454004 A-to-I Human chr16 - 58622192 58622192 58622192 CTCCTGCCTCAGCATCCCTAGTAACTGGGACTACAGGCGCCCACCACCACGCCTGGCTAATTTTT CTCCTGCCTCAGCATCCCTAGTAACTGGGACTCCAGGCGCCCACCACCACGCCTGGCTAATTTTT T G CNOT1 Ensembl:ENSG00000125107 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs970954271 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88886,RMVar_hsa_circ_178791,RMVar_hsa_circ_84450,RMVar_hsa_circ_178834 37969 RMVar_ID_37969 Human_SNP_ID_604454282 A-to-I Human chr16 - 58622816 58622816 58622816 GGGTCAAGAGTTTCACTCTTGGCGCCTGGGTTAGAGTGCAGTGGTGCGATCTCAGCTCACTGCAA GGGTCAAGAGTTTCACTCTTGGCGCCTGGGTTGGAGTGCAGTGGTGCGATCTCAGCTCACTGCAA T C CNOT1 Ensembl:ENSG00000125107 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1450035684 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2478706,Human_RBP_ID_6524348,Human_RBP_ID_12768048,Human_RBP_ID_23164684 RMVar_hsa_circ_88886,RMVar_hsa_circ_178791,RMVar_hsa_circ_84450,RMVar_hsa_circ_178834 37970 RMVar_ID_37970 Human_SNP_ID_604455587 A-to-I Human chr16 - 58627284 58627284 58627284 ATTCTGCCTCAGCCCCTCGAGTAGCTGGGACTACAGGTGCCCGCCACCACACCCAGCTAATTTTT ATTCTGCCTCAGCCCCTCGAGTAGCTGGGACTGCAGGTGCCCGCCACCACACCCAGCTAATTTTT T C CNOT1 Ensembl:ENSG00000125107 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1235131494 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88886,RMVar_hsa_circ_178791,RMVar_hsa_circ_84450,RMVar_hsa_circ_178834 37971 RMVar_ID_37971 Human_SNP_ID_604455802 A-to-I Human chr16 - 58627885 58627885 58627885 AGGCGGAGGTTGCAGTGAGCCGAGATAGAGCTACTGCACTCCAGCCTGGGGGACGGGGAGACTCC AGGCGGAGGTTGCAGTGAGCCGAGATAGAGCTGCTGCACTCCAGCCTGGGGGACGGGGAGACTCC T C CNOT1 Ensembl:ENSG00000125107 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1207460188 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88886,RMVar_hsa_circ_178791,RMVar_hsa_circ_84450,RMVar_hsa_circ_178834 37972 RMVar_ID_37972 Human_SNP_ID_604455855 A-to-I Human chr16 - 58628060 58628060 58628060 ACTTAGGGAGGCCAAGGTAGGTGAATCACCAGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACAT ACTTAGGGAGGCCAAGGTAGGTGAATCACCAGTGGTCAGGAGTTCGAGACCAGCCTGGCCAACAT T A CNOT1 Ensembl:ENSG00000125107 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1206330397 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88886,RMVar_hsa_circ_178791,RMVar_hsa_circ_84450,RMVar_hsa_circ_178834 37973 RMVar_ID_37973 Human_SNP_ID_604464313 A-to-I Human chr16 - 58659787 58659787 58659787 ATTGCTCAAAACTGGGAGGCAGAGGTTGCAGTAAGCCGAGATCGCACCACTGCACTCCAGCCTGG ATTGCTCAAAACTGGGAGGCAGAGGTTGCAGTGAGCCGAGATCGCACCACTGCACTCCAGCCTGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1488606747 Functional Loss SNV dbSNP153 33..33 33 - - - 37974 RMVar_ID_37974 Human_SNP_ID_604477620 A-to-I Human chr16 - 58712277 58712277 58712277 AAACTCCTGACCTCAATGGATCCATCCACCTCAGCCTCCCAAAGTGCTAGGATTATAGACGTGAG AAACTCCTGACCTCAATGGATCCATCCACCTCGGCCTCCCAAAGTGCTAGGATTATAGACGTGAG T C GOT2 Ensembl:ENSG00000125166 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1329044539 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103561,RMVar_hsa_circ_122347,RMVar_hsa_circ_112938,RMVar_hsa_circ_89198,RMVar_hsa_circ_103390,RMVar_hsa_circ_85847,RMVar_hsa_circ_178880,RMVar_hsa_circ_178882,RMVar_hsa_circ_178883,RMVar_hsa_circ_178881,RMVar_hsa_circ_178886,RMVar_hsa_circ_178878,RMVar_hsa_circ_178879,RMVar_hsa_circ_333453,RMVar_hsa_circ_353589,RMVar_hsa_circ_361377,RMVar_hsa_circ_7691 37975 RMVar_ID_37975 Human_SNP_ID_604477634 A-to-I Human chr16 - 58712327 58712327 58712327 CTGTATTTTTAGTAGAGACTGGGTTTCACCACATTGGCCAGGCTGGTCTCAAACTCCTGACCTCA CTGTATTTTTAGTAGAGACTGGGTTTCACCACGTTGGCCAGGCTGGTCTCAAACTCCTGACCTCA T C GOT2 Ensembl:ENSG00000125166 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1441268090 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103561,RMVar_hsa_circ_122347,RMVar_hsa_circ_112938,RMVar_hsa_circ_89198,RMVar_hsa_circ_103390,RMVar_hsa_circ_85847,RMVar_hsa_circ_178880,RMVar_hsa_circ_178882,RMVar_hsa_circ_178883,RMVar_hsa_circ_178881,RMVar_hsa_circ_178886,RMVar_hsa_circ_178878,RMVar_hsa_circ_178879,RMVar_hsa_circ_333453,RMVar_hsa_circ_353589,RMVar_hsa_circ_361377,RMVar_hsa_circ_7691 37976 RMVar_ID_37976 Human_SNP_ID_604477768 A-to-I Human chr16 - 58712853 58712853 58712853 TTAGCACTTCGGCCTCCCAAAGTACTGGGATTACAGGCGTGAACCACTGCGCCCAGCCACCCATT TTAGCACTTCGGCCTCCCAAAGTACTGGGATTTCAGGCGTGAACCACTGCGCCCAGCCACCCATT T A GOT2 Ensembl:ENSG00000125166 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs995210629 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103561,RMVar_hsa_circ_122347,RMVar_hsa_circ_112938,RMVar_hsa_circ_89198,RMVar_hsa_circ_103390,RMVar_hsa_circ_85847,RMVar_hsa_circ_178880,RMVar_hsa_circ_178882,RMVar_hsa_circ_178883,RMVar_hsa_circ_178881,RMVar_hsa_circ_178886,RMVar_hsa_circ_178878,RMVar_hsa_circ_178879,RMVar_hsa_circ_333453,RMVar_hsa_circ_353589,RMVar_hsa_circ_361377,RMVar_hsa_circ_7691 37977 RMVar_ID_37977 Human_SNP_ID_604477833 A-to-I Human chr16 - 58713094 58713094 58713094 TTTTTTGTTTTTTGTGTTTTTGTTTTTGAGACAGAGTTTTGCTCTTGTTGCCCAGGCTGGAGTGC TTTTTTGTTTTTTGTGTTTTTGTTTTTGAGACGGAGTTTTGCTCTTGTTGCCCAGGCTGGAGTGC T C GOT2 Ensembl:ENSG00000125166 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs996614256 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3497151 RMVar_hsa_circ_103561,RMVar_hsa_circ_122347,RMVar_hsa_circ_112938,RMVar_hsa_circ_89198,RMVar_hsa_circ_103390,RMVar_hsa_circ_85847,RMVar_hsa_circ_178880,RMVar_hsa_circ_178882,RMVar_hsa_circ_178883,RMVar_hsa_circ_178881,RMVar_hsa_circ_178886,RMVar_hsa_circ_178878,RMVar_hsa_circ_178879,RMVar_hsa_circ_333453,RMVar_hsa_circ_353589,RMVar_hsa_circ_361377,RMVar_hsa_circ_7691 37978 RMVar_ID_37978 Human_SNP_ID_604478065 A-to-I Human chr16 - 58714205 58714205 58714205 ATCTTACTAAGTTGAATTTAACATACTAAGCCAGGTAAGGTGGCTCACACCTATAATCCCAGCAT ATCTTACTAAGTTGAATTTAACATACTAAGCCGGGTAAGGTGGCTCACACCTATAATCCCAGCAT T C GOT2 Ensembl:ENSG00000125166 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1041962538 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103561,RMVar_hsa_circ_122347,RMVar_hsa_circ_112938,RMVar_hsa_circ_89198,RMVar_hsa_circ_103390,RMVar_hsa_circ_85847,RMVar_hsa_circ_178880,RMVar_hsa_circ_178882,RMVar_hsa_circ_178883,RMVar_hsa_circ_178881,RMVar_hsa_circ_178886,RMVar_hsa_circ_178878,RMVar_hsa_circ_178879,RMVar_hsa_circ_333453,RMVar_hsa_circ_353589,RMVar_hsa_circ_361377,RMVar_hsa_circ_7691 37979 RMVar_ID_37979 Human_SNP_ID_604478085 A-to-I Human chr16 - 58714300 58714300 58714300 GTGAACCACCTGCCTCGGCCTCCCAAAGTGCTAGGATTACAGGCGTGAGCCACCAAGCCCAGCCT GTGAACCACCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCAAGCCCAGCCT T C GOT2 Ensembl:ENSG00000125166 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs549307228 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103561,RMVar_hsa_circ_122347,RMVar_hsa_circ_112938,RMVar_hsa_circ_89198,RMVar_hsa_circ_103390,RMVar_hsa_circ_85847,RMVar_hsa_circ_178880,RMVar_hsa_circ_178882,RMVar_hsa_circ_178883,RMVar_hsa_circ_178881,RMVar_hsa_circ_178886,RMVar_hsa_circ_178878,RMVar_hsa_circ_178879,RMVar_hsa_circ_333453,RMVar_hsa_circ_353589,RMVar_hsa_circ_361377,RMVar_hsa_circ_7691 37980 RMVar_ID_37980 Human_SNP_ID_135337631 A-to-I Human chr3 - 60431128 60431128 60431128 CAGCTCACTGCAGCCTCTGCCTCCAGAGTTCAAGCTATTCTTCTGTCTCAGCTCCCAAGTAGTTT CAGCTCACTGCAGCCTCTGCCTCCAGAGTTCATGCTATTCTTCTGTCTCAGCTCCCAAGTAGTTT T A FHIT Ensembl:ENSG00000189283 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1328360930 Functional Loss SNV dbSNP153 33..33 33 - - - 37981 RMVar_ID_37981 Human_SNP_ID_135366864 A-to-I Human chr3 - 60522226 60522226 60522226 GGCACTTTTAATCCCAGCTTCTCAGGAGGCTGAGACACGATAATTGCTTGAACTCAGGGGGGCAG GGCACTTTTAATCCCAGCTTCTCAGGAGGCTGTGACACGATAATTGCTTGAACTCAGGGGGGCAG T A FHIT Ensembl:ENSG00000189283 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs908241700 Functional Loss SNV dbSNP153 33..33 33 - - - 37982 RMVar_ID_37982 Human_SNP_ID_135430539 A-to-I Human chr3 - 60734646 60734646 60734646 TATACAGAGATTGAGGCCAGGTGGGATGGCTCACCCCTGTAATCCCAGGACTTTGGGAGGCCAAG TATACAGAGATTGAGGCCAGGTGGGATGGCTCGCCCCTGTAATCCCAGGACTTTGGGAGGCCAAG T C FHIT Ensembl:ENSG00000189283 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444485853 Functional Loss SNV dbSNP153 33..33 33 - - - 37983 RMVar_ID_37983 Human_SNP_ID_135547571 A-to-I Human chr3 - 61179453 61179453 61179453 CCTCTCACCTTAGCCACCAAAGTGTTGGGATTACAGATGTGGGTCACTGTGCCTGGACTAATTTT CCTCTCACCTTAGCCACCAAAGTGTTGGGATTGCAGATGTGGGTCACTGTGCCTGGACTAATTTT T C FHIT Ensembl:ENSG00000189283 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs753961768 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56168 37984 RMVar_ID_37984 Human_SNP_ID_135675309 A-to-I Human chr3 + 61655705 61655694 61655706 CCACAGCTCACTCCTGGCTCACTCCTGGGCTCAAGTGATCCTCCTGCCTCAGCCTTCCCTGTAGC CCACAGCTCACTCCTGGCTCAC____________GTGATCCTCCTGCCTCAGCCTTCCCTGTAGC CTCCTGGGCTCAA C PTPRG Ensembl:ENSG00000144724 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1449849577 Functional Loss DEL dbSNP153 23..34 33 - - - RMVar_hsa_circ_97434,RMVar_hsa_circ_114283,RMVar_hsa_circ_219300,RMVar_hsa_circ_219301 37985 RMVar_ID_37985 Human_SNP_ID_135675312 A-to-I Human chr3 + 61655705 61655705 61655705 CCACAGCTCACTCCTGGCTCACTCCTGGGCTCAAGTGATCCTCCTGCCTCAGCCTTCCCTGTAGC CCACAGCTCACTCCTGGCTCACTCCTGGGCTCTAGTGATCCTCCTGCCTCAGCCTTCCCTGTAGC A T PTPRG Ensembl:ENSG00000144724 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1453831825 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97434,RMVar_hsa_circ_114283,RMVar_hsa_circ_219300,RMVar_hsa_circ_219301 37986 RMVar_ID_37986 Human_SNP_ID_135886465 A-to-I Human chr3 - 62417315 62417315 62417315 GCACCACTGCACTCCACCCTGGGCGTCAGAGCAAGACAGTCTCAAAAAAAAAAAAAAAAAAAAAA GCACCACTGCACTCCACCCTGGGCGTCAGAGCGAGACAGTCTCAAAAAAAAAAAAAAAAAAAAAA T C CADPS Ensembl:ENSG00000163618 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1381425420 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7729 37987 RMVar_ID_37987 Human_SNP_ID_135886827 A-to-I Human chr3 - 62418616 62418616 62418616 TATTTATCAGCCGGGCTTGGTGGCTCACACCTATAATGCCAGCACTTTGGGAGGCTGAGGCTGGT TATTTATCAGCCGGGCTTGGTGGCTCACACCTGTAATGCCAGCACTTTGGGAGGCTGAGGCTGGT T C CADPS Ensembl:ENSG00000163618 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs927218145 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25752621 RMVar_hsa_circ_7729 37988 RMVar_ID_37988 Human_SNP_ID_135888349 A-to-I Human chr3 - 62424456 62424456 62424456 TTATCAGGCCAGGCGCGGTGGCTCATGCCTGTAGTACCAGCACTTTGGGAGGCCGAGGCAGGCAA TTATCAGGCCAGGCGCGGTGGCTCATGCCTGTCGTACCAGCACTTTGGGAGGCCGAGGCAGGCAA T G CADPS Ensembl:ENSG00000163618 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1294573955 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7729 37989 RMVar_ID_37989 Human_SNP_ID_136285386 A-to-I Human chr3 + 63903276 63903276 63903276 AATTAGCCGAGCTTGGGCCTGTAGTCCCACCTACCCCGGAGGCTGAGGCAGGAGAATGGCGTGAA AATTAGCCGAGCTTGGGCCTGTAGTCCCACCTGCCCCGGAGGCTGAGGCAGGAGAATGGCGTGAA A G AC104162.2,ATXN7 Ensembl:ENSG00000285399,Ensembl:ENSG00000163635 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886184956 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24383225 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 37990 RMVar_ID_37990 Human_SNP_ID_136291152 A-to-I Human chr3 + 63923624 63923624 63923624 AGTTTAGGAGTTTGAGACCAGCTTGGCAACATAGTGAGACCCCATCTCTACAAAAAAAATTAGCT AGTTTAGGAGTTTGAGACCAGCTTGGCAACATGGTGAGACCCCATCTCTACAAAAAAAATTAGCT A G ATXN7 Ensembl:ENSG00000163635 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs967431943 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 37991 RMVar_ID_37991 Human_SNP_ID_136705496 A-to-I Human chr3 - 65439928 65439886 65439928 AAGAAGCAGCTTGAGCAGCAGCAGCAGCAGCAACAGCAGCAGCAACAGCAGCAGCAGCAGCAGCA AAGAAGCAGCTTGAGCAGCAGCAGCAGCAGCA_________________________________ CTGCTGCTGCTGCTGCTGCTGCTGCTGCTGTTGCTGCTGCTGT C MAGI1 Ensembl:ENSG00000151276 Protein coding CDS GSE56152 embryonic stem cells,wild type - 25708366 RNA-Seq:(High) rs763479364 Functional Loss DEL dbSNP153 33..65 33 - - - Human_RBP_ID_27822350 Human_Splice_Rec_449678,Human_Splice_Rec_449679,Human_Splice_Rec_449724,Human_Splice_Rec_449725,Human_Splice_Rec_449766,Human_Splice_Rec_449767,Human_Splice_Rec_449814,Human_Splice_Rec_449815,Human_Splice_Rec_449856,Human_Splice_Rec_449857,Human_Splice_Rec_449900,Human_Splice_Rec_449901,Human_Splice_Rec_449940,Human_Splice_Rec_449941,Human_Splice_Rec_449984,Human_Splice_Rec_449985,Human_Splice_Rec_450018,Human_Splice_Rec_450019,Human_Splice_Rec_450082,Human_Splice_Rec_450083,Human_Splice_Rec_450092,Human_Splice_Rec_450093,Human_Splice_Rec_450104,Human_Splice_Rec_450105 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_350792,RMVar_hsa_circ_350841,RMVar_hsa_circ_293269,RMVar_hsa_circ_106022,RMVar_hsa_circ_49996,RMVar_hsa_circ_828,RMVar_hsa_circ_22726,RMVar_hsa_circ_104085,RMVar_hsa_circ_267821,RMVar_hsa_circ_219443,RMVar_hsa_circ_341062,RMVar_hsa_circ_301204,RMVar_hsa_circ_379058,RMVar_hsa_circ_283860,RMVar_hsa_circ_319383,RMVar_hsa_circ_337395,RMVar_hsa_circ_351980,RMVar_hsa_circ_288827,RMVar_hsa_circ_219445,RMVar_hsa_circ_219447,RMVar_hsa_circ_70633,RMVar_hsa_circ_219448,RMVar_hsa_circ_219446,RMVar_hsa_circ_294304,RMVar_hsa_circ_326893,RMVar_hsa_circ_347980,RMVar_hsa_circ_61252,RMVar_hsa_circ_283863,RMVar_hsa_circ_54272,RMVar_hsa_circ_219450,RMVar_hsa_circ_219452,RMVar_hsa_circ_219453,RMVar_hsa_circ_219451 37992 RMVar_ID_37992 Human_SNP_ID_136705500 A-to-I Human chr3 - 65439928 65439889 65439928 AAGAAGCAGCTTGAGCAGCAGCAGCAGCAGCAACAGCAGCAGCAACAGCAGCAGCAGCAGCAGCA AAGAAGCAGCTTGAGCAGCAGCAGCAGCAGCA_________________________________ CTGCTGCTGCTGCTGCTGCTGCTGCTGTTGCTGCTGCTGT C MAGI1 Ensembl:ENSG00000151276 Protein coding CDS GSE56152 embryonic stem cells,wild type - 25708366 RNA-Seq:(High) rs1253349373 Functional Loss DEL dbSNP153 33..65 33 - - - Human_RBP_ID_27822350 Human_Splice_Rec_449678,Human_Splice_Rec_449679,Human_Splice_Rec_449724,Human_Splice_Rec_449725,Human_Splice_Rec_449766,Human_Splice_Rec_449767,Human_Splice_Rec_449814,Human_Splice_Rec_449815,Human_Splice_Rec_449856,Human_Splice_Rec_449857,Human_Splice_Rec_449900,Human_Splice_Rec_449901,Human_Splice_Rec_449940,Human_Splice_Rec_449941,Human_Splice_Rec_449984,Human_Splice_Rec_449985,Human_Splice_Rec_450018,Human_Splice_Rec_450019,Human_Splice_Rec_450082,Human_Splice_Rec_450083,Human_Splice_Rec_450092,Human_Splice_Rec_450093,Human_Splice_Rec_450104,Human_Splice_Rec_450105 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_350792,RMVar_hsa_circ_350841,RMVar_hsa_circ_293269,RMVar_hsa_circ_106022,RMVar_hsa_circ_49996,RMVar_hsa_circ_828,RMVar_hsa_circ_22726,RMVar_hsa_circ_104085,RMVar_hsa_circ_267821,RMVar_hsa_circ_219443,RMVar_hsa_circ_341062,RMVar_hsa_circ_301204,RMVar_hsa_circ_379058,RMVar_hsa_circ_283860,RMVar_hsa_circ_319383,RMVar_hsa_circ_337395,RMVar_hsa_circ_351980,RMVar_hsa_circ_288827,RMVar_hsa_circ_219445,RMVar_hsa_circ_219447,RMVar_hsa_circ_70633,RMVar_hsa_circ_219448,RMVar_hsa_circ_219446,RMVar_hsa_circ_294304,RMVar_hsa_circ_326893,RMVar_hsa_circ_347980,RMVar_hsa_circ_61252,RMVar_hsa_circ_283863,RMVar_hsa_circ_54272,RMVar_hsa_circ_219450,RMVar_hsa_circ_219452,RMVar_hsa_circ_219453,RMVar_hsa_circ_219451 37993 RMVar_ID_37993 Human_SNP_ID_136705506 A-to-I Human chr3 - 65439928 65439895 65439928 AAGAAGCAGCTTGAGCAGCAGCAGCAGCAGCAACAGCAGCAGCAACAGCAGCAGCAGCAGCAGCA AAGAAGCAGCTTGAGCAGCAGCAGCAGCAGCA_________________________________ CTGCTGCTGCTGCTGCTGCTGTTGCTGCTGCTGT C MAGI1 Ensembl:ENSG00000151276 Protein coding CDS GSE56152 embryonic stem cells,wild type - 25708366 RNA-Seq:(High) rs756013129 Functional Loss DEL dbSNP153 33..65 33 - - - Human_RBP_ID_27822350 Human_Splice_Rec_449678,Human_Splice_Rec_449679,Human_Splice_Rec_449724,Human_Splice_Rec_449725,Human_Splice_Rec_449766,Human_Splice_Rec_449767,Human_Splice_Rec_449814,Human_Splice_Rec_449815,Human_Splice_Rec_449856,Human_Splice_Rec_449857,Human_Splice_Rec_449900,Human_Splice_Rec_449901,Human_Splice_Rec_449940,Human_Splice_Rec_449941,Human_Splice_Rec_449984,Human_Splice_Rec_449985,Human_Splice_Rec_450018,Human_Splice_Rec_450019,Human_Splice_Rec_450082,Human_Splice_Rec_450083,Human_Splice_Rec_450092,Human_Splice_Rec_450093,Human_Splice_Rec_450104,Human_Splice_Rec_450105 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_350792,RMVar_hsa_circ_350841,RMVar_hsa_circ_293269,RMVar_hsa_circ_106022,RMVar_hsa_circ_49996,RMVar_hsa_circ_828,RMVar_hsa_circ_22726,RMVar_hsa_circ_104085,RMVar_hsa_circ_267821,RMVar_hsa_circ_219443,RMVar_hsa_circ_341062,RMVar_hsa_circ_301204,RMVar_hsa_circ_379058,RMVar_hsa_circ_283860,RMVar_hsa_circ_319383,RMVar_hsa_circ_337395,RMVar_hsa_circ_351980,RMVar_hsa_circ_288827,RMVar_hsa_circ_219445,RMVar_hsa_circ_219447,RMVar_hsa_circ_70633,RMVar_hsa_circ_219448,RMVar_hsa_circ_219446,RMVar_hsa_circ_294304,RMVar_hsa_circ_326893,RMVar_hsa_circ_347980,RMVar_hsa_circ_61252,RMVar_hsa_circ_283863,RMVar_hsa_circ_54272,RMVar_hsa_circ_219450,RMVar_hsa_circ_219452,RMVar_hsa_circ_219453,RMVar_hsa_circ_219451 37994 RMVar_ID_37994 Human_SNP_ID_136705510 A-to-I Human chr3 - 65439928 65439898 65439928 AAGAAGCAGCTTGAGCAGCAGCAGCAGCAGCAACAGCAGCAGCAACAGCAGCAGCAGCAGCAGCA AAGAAGCAGCTTGAGCAGCAGCAGCAGCAGCA______________________________GCA CTGCTGCTGCTGCTGCTGTTGCTGCTGCTGT C MAGI1 Ensembl:ENSG00000151276 Protein coding CDS GSE56152 embryonic stem cells,wild type - 25708366 RNA-Seq:(High) rs777638138 Functional Loss DEL dbSNP153,HGVD 33..62 33 - - - Human_RBP_ID_27822350 Human_Splice_Rec_449678,Human_Splice_Rec_449679,Human_Splice_Rec_449724,Human_Splice_Rec_449725,Human_Splice_Rec_449766,Human_Splice_Rec_449767,Human_Splice_Rec_449814,Human_Splice_Rec_449815,Human_Splice_Rec_449856,Human_Splice_Rec_449857,Human_Splice_Rec_449900,Human_Splice_Rec_449901,Human_Splice_Rec_449940,Human_Splice_Rec_449941,Human_Splice_Rec_449984,Human_Splice_Rec_449985,Human_Splice_Rec_450018,Human_Splice_Rec_450019,Human_Splice_Rec_450082,Human_Splice_Rec_450083,Human_Splice_Rec_450092,Human_Splice_Rec_450093,Human_Splice_Rec_450104,Human_Splice_Rec_450105 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_350792,RMVar_hsa_circ_350841,RMVar_hsa_circ_293269,RMVar_hsa_circ_106022,RMVar_hsa_circ_49996,RMVar_hsa_circ_828,RMVar_hsa_circ_22726,RMVar_hsa_circ_104085,RMVar_hsa_circ_267821,RMVar_hsa_circ_219443,RMVar_hsa_circ_341062,RMVar_hsa_circ_301204,RMVar_hsa_circ_379058,RMVar_hsa_circ_283860,RMVar_hsa_circ_319383,RMVar_hsa_circ_337395,RMVar_hsa_circ_351980,RMVar_hsa_circ_288827,RMVar_hsa_circ_219445,RMVar_hsa_circ_219447,RMVar_hsa_circ_70633,RMVar_hsa_circ_219448,RMVar_hsa_circ_219446,RMVar_hsa_circ_294304,RMVar_hsa_circ_326893,RMVar_hsa_circ_347980,RMVar_hsa_circ_61252,RMVar_hsa_circ_283863,RMVar_hsa_circ_54272,RMVar_hsa_circ_219450,RMVar_hsa_circ_219452,RMVar_hsa_circ_219453,RMVar_hsa_circ_219451 37995 RMVar_ID_37995 Human_SNP_ID_136705519 A-to-I Human chr3 - 65439928 65439904 65439928 AAGAAGCAGCTTGAGCAGCAGCAGCAGCAGCAACAGCAGCAGCAACAGCAGCAGCAGCAGCAGCA AAGAAGCAGCTTGAGCAGCAGCAGCAGCAGCA________________________GCAGCAGCA CTGCTGCTGCTGTTGCTGCTGCTGT C MAGI1 Ensembl:ENSG00000151276 Protein coding CDS GSE56152 embryonic stem cells,wild type - 25708366 RNA-Seq:(High) rs747189565 Functional Loss DEL dbSNP153 33..56 33 - - - Human_RBP_ID_27822350 Human_Splice_Rec_449678,Human_Splice_Rec_449679,Human_Splice_Rec_449724,Human_Splice_Rec_449725,Human_Splice_Rec_449766,Human_Splice_Rec_449767,Human_Splice_Rec_449814,Human_Splice_Rec_449815,Human_Splice_Rec_449856,Human_Splice_Rec_449857,Human_Splice_Rec_449900,Human_Splice_Rec_449901,Human_Splice_Rec_449940,Human_Splice_Rec_449941,Human_Splice_Rec_449984,Human_Splice_Rec_449985,Human_Splice_Rec_450018,Human_Splice_Rec_450019,Human_Splice_Rec_450082,Human_Splice_Rec_450083,Human_Splice_Rec_450092,Human_Splice_Rec_450093,Human_Splice_Rec_450104,Human_Splice_Rec_450105 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_350792,RMVar_hsa_circ_350841,RMVar_hsa_circ_293269,RMVar_hsa_circ_106022,RMVar_hsa_circ_49996,RMVar_hsa_circ_828,RMVar_hsa_circ_22726,RMVar_hsa_circ_104085,RMVar_hsa_circ_267821,RMVar_hsa_circ_219443,RMVar_hsa_circ_341062,RMVar_hsa_circ_301204,RMVar_hsa_circ_379058,RMVar_hsa_circ_283860,RMVar_hsa_circ_319383,RMVar_hsa_circ_337395,RMVar_hsa_circ_351980,RMVar_hsa_circ_288827,RMVar_hsa_circ_219445,RMVar_hsa_circ_219447,RMVar_hsa_circ_70633,RMVar_hsa_circ_219448,RMVar_hsa_circ_219446,RMVar_hsa_circ_294304,RMVar_hsa_circ_326893,RMVar_hsa_circ_347980,RMVar_hsa_circ_61252,RMVar_hsa_circ_283863,RMVar_hsa_circ_54272,RMVar_hsa_circ_219450,RMVar_hsa_circ_219452,RMVar_hsa_circ_219453,RMVar_hsa_circ_219451 37996 RMVar_ID_37996 Human_SNP_ID_136705520 A-to-I Human chr3 - 65439928 65439904 65439928 AAGAAGCAGCTTGAGCAGCAGCAGCAGCAGCAACAGCAGCAGCAACAGCAGCAGCAGCAGCAGCA AAGAAGCAGCTTGAGCAGCAGCAGCAGCAGCA____________ACAGCAGCAGCAGCAGCAGCA CTGCTGCTGCTGTTGCTGCTGCTGT CTGCTGCTGCTGT MAGI1 Ensembl:ENSG00000151276 Protein coding CDS GSE56152 embryonic stem cells,wild type - 25708366 RNA-Seq:(High) rs747189565 Functional Loss DEL dbSNP153 33..44 33 - - - Human_RBP_ID_27822350 Human_Splice_Rec_449678,Human_Splice_Rec_449679,Human_Splice_Rec_449724,Human_Splice_Rec_449725,Human_Splice_Rec_449766,Human_Splice_Rec_449767,Human_Splice_Rec_449814,Human_Splice_Rec_449815,Human_Splice_Rec_449856,Human_Splice_Rec_449857,Human_Splice_Rec_449900,Human_Splice_Rec_449901,Human_Splice_Rec_449940,Human_Splice_Rec_449941,Human_Splice_Rec_449984,Human_Splice_Rec_449985,Human_Splice_Rec_450018,Human_Splice_Rec_450019,Human_Splice_Rec_450082,Human_Splice_Rec_450083,Human_Splice_Rec_450092,Human_Splice_Rec_450093,Human_Splice_Rec_450104,Human_Splice_Rec_450105 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_350792,RMVar_hsa_circ_350841,RMVar_hsa_circ_293269,RMVar_hsa_circ_106022,RMVar_hsa_circ_49996,RMVar_hsa_circ_828,RMVar_hsa_circ_22726,RMVar_hsa_circ_104085,RMVar_hsa_circ_267821,RMVar_hsa_circ_219443,RMVar_hsa_circ_341062,RMVar_hsa_circ_301204,RMVar_hsa_circ_379058,RMVar_hsa_circ_283860,RMVar_hsa_circ_319383,RMVar_hsa_circ_337395,RMVar_hsa_circ_351980,RMVar_hsa_circ_288827,RMVar_hsa_circ_219445,RMVar_hsa_circ_219447,RMVar_hsa_circ_70633,RMVar_hsa_circ_219448,RMVar_hsa_circ_219446,RMVar_hsa_circ_294304,RMVar_hsa_circ_326893,RMVar_hsa_circ_347980,RMVar_hsa_circ_61252,RMVar_hsa_circ_283863,RMVar_hsa_circ_54272,RMVar_hsa_circ_219450,RMVar_hsa_circ_219452,RMVar_hsa_circ_219453,RMVar_hsa_circ_219451 37997 RMVar_ID_37997 Human_SNP_ID_136705544 A-to-I Human chr3 - 65439928 65439922 65439928 AAGAAGCAGCTTGAGCAGCAGCAGCAGCAGCAACAGCAGCAGCAACAGCAGCAGCAGCAGCAGCA AAGAAGCAGCTTGAGCAGCAGCAGCAGCAGCA______GCAGCAACAGCAGCAGCAGCAGCAGCA CTGCTGT C MAGI1 Ensembl:ENSG00000151276 Protein coding CDS GSE56152 embryonic stem cells,wild type - 25708366 RNA-Seq:(High) rs1189084936 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_27822350 Human_Splice_Rec_449678,Human_Splice_Rec_449679,Human_Splice_Rec_449724,Human_Splice_Rec_449725,Human_Splice_Rec_449766,Human_Splice_Rec_449767,Human_Splice_Rec_449814,Human_Splice_Rec_449815,Human_Splice_Rec_449856,Human_Splice_Rec_449857,Human_Splice_Rec_449900,Human_Splice_Rec_449901,Human_Splice_Rec_449940,Human_Splice_Rec_449941,Human_Splice_Rec_449984,Human_Splice_Rec_449985,Human_Splice_Rec_450018,Human_Splice_Rec_450019,Human_Splice_Rec_450082,Human_Splice_Rec_450083,Human_Splice_Rec_450092,Human_Splice_Rec_450093,Human_Splice_Rec_450104,Human_Splice_Rec_450105 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_350792,RMVar_hsa_circ_350841,RMVar_hsa_circ_293269,RMVar_hsa_circ_106022,RMVar_hsa_circ_49996,RMVar_hsa_circ_828,RMVar_hsa_circ_22726,RMVar_hsa_circ_104085,RMVar_hsa_circ_267821,RMVar_hsa_circ_219443,RMVar_hsa_circ_341062,RMVar_hsa_circ_301204,RMVar_hsa_circ_379058,RMVar_hsa_circ_283860,RMVar_hsa_circ_319383,RMVar_hsa_circ_337395,RMVar_hsa_circ_351980,RMVar_hsa_circ_288827,RMVar_hsa_circ_219445,RMVar_hsa_circ_219447,RMVar_hsa_circ_70633,RMVar_hsa_circ_219448,RMVar_hsa_circ_219446,RMVar_hsa_circ_294304,RMVar_hsa_circ_326893,RMVar_hsa_circ_347980,RMVar_hsa_circ_61252,RMVar_hsa_circ_283863,RMVar_hsa_circ_54272,RMVar_hsa_circ_219450,RMVar_hsa_circ_219452,RMVar_hsa_circ_219453,RMVar_hsa_circ_219451 37998 RMVar_ID_37998 Human_SNP_ID_136705549 A-to-I Human chr3 - 65439928 65439928 65439928 AAGAAGCAGCTTGAGCAGCAGCAGCAGCAGCAACAGCAGCAGCAACAGCAGCAGCAGCAGCAGCA AAGAAGCAGCTTGAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAACAGCAGCAGCAGCAGCAGCA T C MAGI1 Ensembl:ENSG00000151276 Protein coding CDS GSE56152 embryonic stem cells,wild type - 25708366 RNA-Seq:(High) rs62642828 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27822350 Human_Splice_Rec_449678,Human_Splice_Rec_449679,Human_Splice_Rec_449724,Human_Splice_Rec_449725,Human_Splice_Rec_449766,Human_Splice_Rec_449767,Human_Splice_Rec_449814,Human_Splice_Rec_449815,Human_Splice_Rec_449856,Human_Splice_Rec_449857,Human_Splice_Rec_449900,Human_Splice_Rec_449901,Human_Splice_Rec_449940,Human_Splice_Rec_449941,Human_Splice_Rec_449984,Human_Splice_Rec_449985,Human_Splice_Rec_450018,Human_Splice_Rec_450019,Human_Splice_Rec_450082,Human_Splice_Rec_450083,Human_Splice_Rec_450092,Human_Splice_Rec_450093,Human_Splice_Rec_450104,Human_Splice_Rec_450105 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_350792,RMVar_hsa_circ_350841,RMVar_hsa_circ_293269,RMVar_hsa_circ_106022,RMVar_hsa_circ_49996,RMVar_hsa_circ_828,RMVar_hsa_circ_22726,RMVar_hsa_circ_104085,RMVar_hsa_circ_267821,RMVar_hsa_circ_219443,RMVar_hsa_circ_341062,RMVar_hsa_circ_301204,RMVar_hsa_circ_379058,RMVar_hsa_circ_283860,RMVar_hsa_circ_319383,RMVar_hsa_circ_337395,RMVar_hsa_circ_351980,RMVar_hsa_circ_288827,RMVar_hsa_circ_219445,RMVar_hsa_circ_219447,RMVar_hsa_circ_70633,RMVar_hsa_circ_219448,RMVar_hsa_circ_219446,RMVar_hsa_circ_294304,RMVar_hsa_circ_326893,RMVar_hsa_circ_347980,RMVar_hsa_circ_61252,RMVar_hsa_circ_283863,RMVar_hsa_circ_54272,RMVar_hsa_circ_219450,RMVar_hsa_circ_219452,RMVar_hsa_circ_219453,RMVar_hsa_circ_219451 37999 RMVar_ID_37999 Human_SNP_ID_136742431 A-to-I Human chr3 - 65570256 65570256 65570256 CTCTACTAAAAACATAAAAATTAGCTGGATATAGTGGTGCATGTCTGTAGTCCCAGCCACTTGGA CTCTACTAAAAACATAAAAATTAGCTGGATATGGTGGTGCATGTCTGTAGTCCCAGCCACTTGGA T C MAGI1 Ensembl:ENSG00000151276 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1405928264 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8578027 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 38000 RMVar_ID_38000 Human_SNP_ID_136807453 A-to-I Human chr3 - 65808412 65808412 65808412 TGACTGTAACCTCTGCCTCCCAGCTTCAAGCTATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGA TGACTGTAACCTCTGCCTCCCAGCTTCAAGCTGTTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGA T C MAGI1 Ensembl:ENSG00000151276 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1016911247 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106022,RMVar_hsa_circ_219443,RMVar_hsa_circ_87074,RMVar_hsa_circ_219454,RMVar_hsa_circ_57399 38001 RMVar_ID_38001 Human_SNP_ID_136807454 A-to-I Human chr3 - 65808417 65808417 65808417 TTGGGTGACTGTAACCTCTGCCTCCCAGCTTCAAGCTATTCTCCTGCCTCAGCCTCCTGAGTAGC TTGGGTGACTGTAACCTCTGCCTCCCAGCTTCGAGCTATTCTCCTGCCTCAGCCTCCTGAGTAGC T C MAGI1 Ensembl:ENSG00000151276 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1306623206 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106022,RMVar_hsa_circ_219443,RMVar_hsa_circ_87074,RMVar_hsa_circ_219454,RMVar_hsa_circ_57399 38002 RMVar_ID_38002 Human_SNP_ID_136826926 A-to-I Human chr3 - 65877667 65877667 65877667 TCTGTAATCCCAGCCACTTGGGAGGCTTAGGCAGGAGAATTGCTTGAACCTGGGAATCAGTTAAA TCTGTAATCCCAGCCACTTGGGAGGCTTAGGCCGGAGAATTGCTTGAACCTGGGAATCAGTTAAA T G MAGI1,MAGI1-IT1 Ensembl:ENSG00000151276,Ensembl:ENSG00000272610 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1052768366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17573736,Human_RBP_ID_25753199 RMVar_hsa_circ_106022,RMVar_hsa_circ_219443,RMVar_hsa_circ_87074,RMVar_hsa_circ_219454,RMVar_hsa_circ_57399 38003 RMVar_ID_38003 Human_SNP_ID_136835678 A-to-I Human chr3 - 65910996 65910996 65910996 AAAATTAGCCGGGTGTGCTGGCGTGCACCTGTAGTCCCAGCCACTCAGGAGGCTGAGGCAGGAGA AAAATTAGCCGGGTGTGCTGGCGTGCACCTGTGGTCCCAGCCACTCAGGAGGCTGAGGCAGGAGA T C MAGI1,MAGI1-IT1 Ensembl:ENSG00000151276,Ensembl:ENSG00000272610 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs889619669 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106022,RMVar_hsa_circ_219443,RMVar_hsa_circ_87074,RMVar_hsa_circ_219454 38004 RMVar_ID_38004 Human_SNP_ID_136838415 A-to-I Human chr3 - 65921411 65921411 65921411 CCAGCTACTCGGGAGGCTGAGATGGGAGAATTACTTGAACCCGGGACACAGAGATTGCAGTAAGC CCAGCTACTCGGGAGGCTGAGATGGGAGAATTTCTTGAACCCGGGACACAGAGATTGCAGTAAGC T A MAGI1,MAGI1-IT1 Ensembl:ENSG00000151276,Ensembl:ENSG00000272610 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs762319452 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106022,RMVar_hsa_circ_219443,RMVar_hsa_circ_87074,RMVar_hsa_circ_219454 38005 RMVar_ID_38005 Human_SNP_ID_136839691 A-to-I Human chr3 - 65925818 65925818 65925818 AAAATTGGCAGAGTGTGGTGGCTCGTGACTGTAGTCCTAGCTACTCAGGAGGCTGAGGTGAGAGG AAAATTGGCAGAGTGTGGTGGCTCGTGACTGTGGTCCTAGCTACTCAGGAGGCTGAGGTGAGAGG T C MAGI1,MAGI1-IT1 Ensembl:ENSG00000151276,Ensembl:ENSG00000272610 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1233645319 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106022,RMVar_hsa_circ_219443,RMVar_hsa_circ_87074,RMVar_hsa_circ_219454 38006 RMVar_ID_38006 Human_SNP_ID_136848760 A-to-I Human chr3 - 65958935 65958935 65958935 TTGGCCAAGCTGGAGTGCAGTGGCACGATCTCAGCTCACTGTATCCTCTGCCTTCGGGGTTCAAA TTGGCCAAGCTGGAGTGCAGTGGCACGATCTCCGCTCACTGTATCCTCTGCCTTCGGGGTTCAAA T G MAGI1 Ensembl:ENSG00000151276 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1195219100 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14928959,Human_RBP_ID_23025046 RMVar_hsa_circ_106022,RMVar_hsa_circ_219443,RMVar_hsa_circ_87074,RMVar_hsa_circ_219454 38007 RMVar_ID_38007 Human_SNP_ID_136856570 A-to-I Human chr3 - 65986999 65986999 65986999 GAACATGGTGGCGTATACCTGTAGTCCCAGCTACTCTGGAAACTGAGGCAGGAAAATCACTTGAA GAACATGGTGGCGTATACCTGTAGTCCCAGCTGCTCTGGAAACTGAGGCAGGAAAATCACTTGAA T C MAGI1 Ensembl:ENSG00000151276 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs766637241 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106022,RMVar_hsa_circ_219443,RMVar_hsa_circ_87074,RMVar_hsa_circ_219454 38008 RMVar_ID_38008 Human_SNP_ID_136856758 A-to-I Human chr3 - 65987625 65987625 65987625 ATGCCATTGCACTCCAGCCTGGGTGACAGAGTAAGACTCTGCCTTAAAAAAGAAAGGAAAGAAAA ATGCCATTGCACTCCAGCCTGGGTGACAGAGTGAGACTCTGCCTTAAAAAAGAAAGGAAAGAAAA T C MAGI1 Ensembl:ENSG00000151276 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1026242350 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106022,RMVar_hsa_circ_219443,RMVar_hsa_circ_87074,RMVar_hsa_circ_219454 38009 RMVar_ID_38009 Human_SNP_ID_136857634 A-to-I Human chr3 - 65990935 65990935 65990935 TCACCCAGGCTGGAGTGCAGTGATATGATCATAGGTCACTGCAGGCTCAAACTCCTGGGCTCAAG TCACCCAGGCTGGAGTGCAGTGATATGATCATGGGTCACTGCAGGCTCAAACTCCTGGGCTCAAG T C MAGI1 Ensembl:ENSG00000151276 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1178748007 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106022,RMVar_hsa_circ_219443,RMVar_hsa_circ_87074,RMVar_hsa_circ_219454 38010 RMVar_ID_38010 Human_SNP_ID_136858936 A-to-I Human chr3 - 65995882 65995882 65995882 GAGATCCTCCTGCCTCAGCCTCCTGAATAGCTAGGACTACAGGTGCATGCTACCACACGCAGCTA GAGATCCTCCTGCCTCAGCCTCCTGAATAGCTGGGACTACAGGTGCATGCTACCACACGCAGCTA T C MAGI1 Ensembl:ENSG00000151276 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1230842859 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106022,RMVar_hsa_circ_219443,RMVar_hsa_circ_87074,RMVar_hsa_circ_219454 38011 RMVar_ID_38011 Human_SNP_ID_136867632 A-to-I Human chr3 - 66027396 66027396 66027396 GGGAGGCTGTGGTGGGAGGATTGCTTGAGCCAAGGAGTCCGAGGCTGCAGTGAGCTATGATGGAA GGGAGGCTGTGGTGGGAGGATTGCTTGAGCCAGGGAGTCCGAGGCTGCAGTGAGCTATGATGGAA T C MAGI1 Ensembl:ENSG00000151276 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1208243425 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106022,RMVar_hsa_circ_219443,RMVar_hsa_circ_87074,RMVar_hsa_circ_219454 38012 RMVar_ID_38012 Human_SNP_ID_136869071 A-to-I Human chr3 - 66032852 66032852 66032852 GGAGTGCAGTGGTGCGATCTCGGCTCACTGCAACCTTTGCCTCCCGGGTTCAAGCAATTCTGATG GGAGTGCAGTGGTGCGATCTCGGCTCACTGCATCCTTTGCCTCCCGGGTTCAAGCAATTCTGATG T A MAGI1 Ensembl:ENSG00000151276 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1358566175 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106022,RMVar_hsa_circ_219443,RMVar_hsa_circ_87074,RMVar_hsa_circ_219454 38013 RMVar_ID_38013 Human_SNP_ID_136869072 A-to-I Human chr3 - 66032852 66032852 66032852 GGAGTGCAGTGGTGCGATCTCGGCTCACTGCAACCTTTGCCTCCCGGGTTCAAGCAATTCTGATG GGAGTGCAGTGGTGCGATCTCGGCTCACTGCAGCCTTTGCCTCCCGGGTTCAAGCAATTCTGATG T C MAGI1 Ensembl:ENSG00000151276 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1358566175 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106022,RMVar_hsa_circ_219443,RMVar_hsa_circ_87074,RMVar_hsa_circ_219454 38014 RMVar_ID_38014 Human_SNP_ID_136970314 A-to-I Human chr3 - 66391260 66391260 66391260 GTCATACGCTAACTCTGTGCTCAGCTTTTTTGAGGGACTGCCAAACTGTTTTCCAGAGTGGCTTC GTCATACGCTAACTCTGTGCTCAGCTTTTTTGGGGGACTGCCAAACTGTTTTCCAGAGTGGCTTC T C LRIG1 Ensembl:ENSG00000144749 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1409250608 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265580,RMVar_hsa_circ_219475,RMVar_hsa_circ_118420,RMVar_hsa_circ_267570,RMVar_hsa_circ_219476,RMVar_hsa_circ_91816,RMVar_hsa_circ_269168,RMVar_hsa_circ_271862,RMVar_hsa_circ_376604,RMVar_hsa_circ_34311,RMVar_hsa_circ_219477,RMVar_hsa_circ_219478 38015 RMVar_ID_38015 Human_SNP_ID_137268876 A-to-I Human chr3 - 67491532 67491532 67491532 GGTAAAACCCCGTCTCTACTTAAAATGCAAAAATTAGCCAGGCGTGGTTGCAGGCACCTATAATT GGTAAAACCCCGTCTCTACTTAAAATGCAAAAGTTAGCCAGGCGTGGTTGCAGGCACCTATAATT T C SUCLG2 Ensembl:ENSG00000172340 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1336911889 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24963,RMVar_hsa_circ_323048,RMVar_hsa_circ_358861,RMVar_hsa_circ_367299,RMVar_hsa_circ_354090,RMVar_hsa_circ_96448,RMVar_hsa_circ_219505,RMVar_hsa_circ_219506 38016 RMVar_ID_38016 Human_SNP_ID_137298099 A-to-I Human chr3 - 67605978 67605978 67605978 CCCAGTTTGGCCTCAAGTGATCTTCCTGCCTCAGCCTCTCAAAGTGCTGAGATTACAACCGAGAG CCCAGTTTGGCCTCAAGTGATCTTCCTGCCTCCGCCTCTCAAAGTGCTGAGATTACAACCGAGAG T G SUCLG2 Ensembl:ENSG00000172340 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs551501314 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_367299,RMVar_hsa_circ_219507,RMVar_hsa_circ_342476,RMVar_hsa_circ_353461,RMVar_hsa_circ_282783,RMVar_hsa_circ_219518,RMVar_hsa_circ_358757,RMVar_hsa_circ_219520 38017 RMVar_ID_38017 Human_SNP_ID_137298849 A-to-I Human chr3 - 67608824 67608824 67608824 AAACTAAAAAAATTAGCCTAGTATGGTGGTGTATGCCTGTAGTCCTAGCTACTCTGGAGGCTTTG AAACTAAAAAAATTAGCCTAGTATGGTGGTGTGTGCCTGTAGTCCTAGCTACTCTGGAGGCTTTG T C SUCLG2 Ensembl:ENSG00000172340 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1331579775 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_367299,RMVar_hsa_circ_219507,RMVar_hsa_circ_342476,RMVar_hsa_circ_353461,RMVar_hsa_circ_282783,RMVar_hsa_circ_219518,RMVar_hsa_circ_358757,RMVar_hsa_circ_219520 38018 RMVar_ID_38018 Human_SNP_ID_137313404 A-to-I Human chr3 + 67662305 67662305 67662305 CCTGTAATCCCAGCTACTTGGGAGGCAGGGGCAGGAGAATCACTTGAATCCAGGAGGCAGAGGTT CCTGTAATCCCAGCTACTTGGGAGGCAGGGGCTGGAGAATCACTTGAATCCAGGAGGCAGAGGTT A T SUCLG2-AS1 Ensembl:ENSG00000241316 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs761095567 Functional Loss SNV dbSNP153 33..33 33 - - - 38019 RMVar_ID_38019 Human_SNP_ID_137440279 A-to-I Human chr3 + 68145352 68145352 68145352 TGGAAGCACTTAGAGATGCAACAAGGAGACGCACCTTTGCCCTGGTCTCTCAAGCATATACTTCA TGGAAGCACTTAGAGATGCAACAAGGAGACGCGCCTTTGCCCTGGTCTCTCAAGCATATACTTCA A G COPS8P2,TAFA1 Ensembl:ENSG00000214552,Ensembl:ENSG00000183662 Pseudogene,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs11553714 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7237480,Human_RBP_ID_17405137 Human_miRNA_ID_1834671,Human_miRNA_ID_1834777,Human_miRNA_ID_1879290 38020 RMVar_ID_38020 Human_SNP_ID_137677462 A-to-I Human chr3 - 69026409 69026400 69026409 TATTTTTAGTAGAGACGAGGTTTTTCCATGTTAGTCAAGTTGGTCTTGATCTCCCAACCTCAGGT TATTTTTAGTAGAGACGAGGTTTTTCCATGTT_________GGTCTTGATCTCCCAACCTCAGGT CAACTTGACT C TMF1 Ensembl:ENSG00000144747 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1258063201 Functional Loss DEL dbSNP153 33..41 33 - - - 38021 RMVar_ID_38021 Human_SNP_ID_137677691 A-to-I Human chr3 - 69027223 69027223 69027223 GAGAGGCTGAGGTAGGTGGATCACTTGAGGCTAAGAGTTCAAGACCAGCCTGGCCAACATGGCAA GAGAGGCTGAGGTAGGTGGATCACTTGAGGCTGAGAGTTCAAGACCAGCCTGGCCAACATGGCAA T C TMF1 Ensembl:ENSG00000144747 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1458836733 Functional Loss SNV dbSNP153 33..33 33 - - - 38022 RMVar_ID_38022 Human_SNP_ID_137685715 A-to-I Human chr3 - 69057281 69057281 69057281 TCAGGGGTAGTAAAAAGAATCATTCCTGCAGTAGCTTCCACAAATGCAGTCATTGCAGGTGAGGA TCAGGGGTAGTAAAAAGAATCATTCCTGCAGTCGCTTCCACAAATGCAGTCATTGCAGGTGAGGA T G UBA3 Ensembl:ENSG00000144744 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs750292115 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5390180,Human_RBP_ID_18814008,Human_RBP_ID_25762891 Human_Splice_Rec_451014,Human_Splice_Rec_451015,Human_Splice_Rec_451044,Human_Splice_Rec_451045,Human_Splice_Rec_451076,Human_Splice_Rec_451077,Human_Splice_Rec_451100,Human_Splice_Rec_451101,Human_Splice_Rec_451128,Human_Splice_Rec_451129 Human_miRNA_ID_621098,Human_miRNA_ID_2234136,Human_miRNA_ID_3028292 RMVar_hsa_circ_126849,RMVar_hsa_circ_19230,RMVar_hsa_circ_219556,RMVar_hsa_circ_266956,RMVar_hsa_circ_2701,RMVar_hsa_circ_86340,RMVar_hsa_circ_324803,RMVar_hsa_circ_219557 38023 RMVar_ID_38023 Human_SNP_ID_137694184 A-to-I Human chr3 + 69091087 69091086 69091087 TGGCGTGGTGGCATGCATCTGTGGTCCCAGCTACTTGGGAGGCTGAGGTGGGAGGATCTTTTGAG TGGCGTGGTGGCATGCATCTGTGGTCCCAGCT_CTTGGGAGGCTGAGGTGGGAGGATCTTTTGAG TA T ARL6IP5 Ensembl:ENSG00000144746 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1269512455 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_123032,RMVar_hsa_circ_219562 38024 RMVar_ID_38024 Human_SNP_ID_137733621 A-to-I Human chr3 - 69231569 69231569 69231569 GAAGGATGCAGCTGGGCCGGGCACAGTGGCTTACGCCTGTAATCCCAGCACTTTGGGAGGTGGAG GAAGGATGCAGCTGGGCCGGGCACAGTGGCTTTCGCCTGTAATCCCAGCACTTTGGGAGGTGGAG T A FRMD4B Ensembl:ENSG00000114541 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042858006 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73296,RMVar_hsa_circ_65267,RMVar_hsa_circ_69116,RMVar_hsa_circ_20150,RMVar_hsa_circ_315266,RMVar_hsa_circ_25160,RMVar_hsa_circ_219576,RMVar_hsa_circ_219577,RMVar_hsa_circ_68476 38025 RMVar_ID_38025 Human_SNP_ID_137733622 A-to-I Human chr3 - 69231569 69231569 69231569 GAAGGATGCAGCTGGGCCGGGCACAGTGGCTTACGCCTGTAATCCCAGCACTTTGGGAGGTGGAG GAAGGATGCAGCTGGGCCGGGCACAGTGGCTTCCGCCTGTAATCCCAGCACTTTGGGAGGTGGAG T G FRMD4B Ensembl:ENSG00000114541 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042858006 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73296,RMVar_hsa_circ_65267,RMVar_hsa_circ_69116,RMVar_hsa_circ_20150,RMVar_hsa_circ_315266,RMVar_hsa_circ_25160,RMVar_hsa_circ_219576,RMVar_hsa_circ_219577,RMVar_hsa_circ_68476 38026 RMVar_ID_38026 Human_SNP_ID_137744666 A-to-I Human chr3 - 69270694 69270694 69270694 GGGCATGATGGCGGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACCTGAA GGGCATGATGGCGGGCGCCTGTAGTCCCAGCTGCTCGGGAGGCTGAGGCAGGAGAATCACCTGAA T C FRMD4B Ensembl:ENSG00000114541 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1242844949 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25263,RMVar_hsa_circ_69116,RMVar_hsa_circ_20150,RMVar_hsa_circ_25160,RMVar_hsa_circ_219577 38027 RMVar_ID_38027 Human_SNP_ID_137744667 A-to-I Human chr3 - 69270698 69270698 69270698 AGCCGGGCATGATGGCGGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACC AGCCGGGCATGATGGCGGGCGCCTGTAGTCCCCGCTACTCGGGAGGCTGAGGCAGGAGAATCACC T G FRMD4B Ensembl:ENSG00000114541 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs930536782 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25263,RMVar_hsa_circ_69116,RMVar_hsa_circ_20150,RMVar_hsa_circ_25160,RMVar_hsa_circ_219577 38028 RMVar_ID_38028 Human_SNP_ID_137887799 A-to-I Human chr3 + 69812886 69812886 69812886 GGGCAATGGGAAAGGTTTACAATTGGAAAGGAAAGTTGGTGTAGGTCTTTCCAGCAGTAAAATCT GGGCAATGGGAAAGGTTTACAATTGGAAAGGAGAGTTGGTGTAGGTCTTTCCAGCAGTAAAATCT A G MITF Ensembl:ENSG00000187098 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1385906391 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_368653 38029 RMVar_ID_38029 Human_SNP_ID_137920591 A-to-I Human chr3 + 69950158 69950158 69950158 AACAACAAAAGCAAGAATCGTCGGGCAGGCACAGTAGCTCACGCCTGTAATCTCAGCACTTTGGG AACAACAAAAGCAAGAATCGTCGGGCAGGCACGGTAGCTCACGCCTGTAATCTCAGCACTTTGGG A G MITF Ensembl:ENSG00000187098 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs777695598 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84118,RMVar_hsa_circ_342088,RMVar_hsa_circ_101040,RMVar_hsa_circ_219589,RMVar_hsa_circ_219590 38030 RMVar_ID_38030 Human_SNP_ID_137925337 A-to-I Human chr3 + 69968266 69968266 69968266 GTATGGTCCATAGCACTGTATATTATGGATCGATATTAATGTATCCAATGAAATAATCGACTTGT GTATGGTCCATAGCACTGTATATTATGGATCGTTATTAATGTATCCAATGAAATAATCGACTTGT A T MITF Ensembl:ENSG00000187098 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1035756023 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_607681,Human_RBP_ID_1631201,Human_RBP_ID_18814070,Human_RBP_ID_21897563,Human_RBP_ID_27720588 Human_miRNA_ID_128070,Human_miRNA_ID_3098806 RMVar_hsa_circ_84118,RMVar_hsa_circ_219590,RMVar_hsa_circ_267730 38031 RMVar_ID_38031 Human_SNP_ID_138185561 A-to-I Human chr3 - 70961836 70961836 70961836 GGCTGGACTCGAACTCCTGGGCTCAAGTGATCATCCTACCTTAGCCTCCCAAGTAACTTGGACTA GGCTGGACTCGAACTCCTGGGCTCAAGTGATCCTCCTACCTTAGCCTCCCAAGTAACTTGGACTA T G AC097634.4,FOXP1 Ensembl:ENSG00000285708,Ensembl:ENSG00000114861 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1351180086 Functional Loss SNV dbSNP153 33..33 33 - - - 38032 RMVar_ID_38032 Human_SNP_ID_138244458 A-to-I Human chr3 - 71187393 71187393 71187393 TTAGTAGAGACAGGGTTTCACCATGTTGTCCAAGCTGGTCTCAAACTCCTGACCTCAGGTGATCC TTAGTAGAGACAGGGTTTCACCATGTTGTCCACGCTGGTCTCAAACTCCTGACCTCAGGTGATCC T G AC097634.4,FOXP1 Ensembl:ENSG00000285708,Ensembl:ENSG00000114861 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs912111676 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82550,RMVar_hsa_circ_219594,RMVar_hsa_circ_219604,RMVar_hsa_circ_73032,RMVar_hsa_circ_83199,RMVar_hsa_circ_70236,RMVar_hsa_circ_316285,RMVar_hsa_circ_54457,RMVar_hsa_circ_64045,RMVar_hsa_circ_219614,RMVar_hsa_circ_333764,RMVar_hsa_circ_346502,RMVar_hsa_circ_336895,RMVar_hsa_circ_286827 38033 RMVar_ID_38033 Human_SNP_ID_138253084 A-to-I Human chr3 - 71222143 71222143 71222143 GTTTGTTTGTTTGTTTGTTTTTTTGATACGGAATCTCGCTCTGGCACCAGGCTGGAGTGCAGTGT GTTTGTTTGTTTGTTTGTTTTTTTGATACGGAGTCTCGCTCTGGCACCAGGCTGGAGTGCAGTGT T C AC097634.4,FOXP1 Ensembl:ENSG00000285708,Ensembl:ENSG00000114861 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1306791393 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_277933 38034 RMVar_ID_38034 Human_SNP_ID_138253184 A-to-I Human chr3 - 71222535 71222535 71222535 GGGCACCTGTAATCCCAGCTACTCTGGAGGCTAAGGCATGAGAATTGCTTGAACCTGAGAGGCAG GGGCACCTGTAATCCCAGCTACTCTGGAGGCTGAGGCATGAGAATTGCTTGAACCTGAGAGGCAG T C AC097634.4,FOXP1 Ensembl:ENSG00000285708,Ensembl:ENSG00000114861 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1447187998 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_277933 38035 RMVar_ID_38035 Human_SNP_ID_138340086 A-to-I Human chr3 - 71559609 71559608 71559609 ACTTCTAGGCTCAAGTGATCTGTCCCTGCTTCAGCCTCCCAAAGTGTTGGGATTACAAGTATGAG ACTTCTAGGCTCAAGTGATCTGTCCCTGCTTC_GCCTCCCAAAGTGTTGGGATTACAAGTATGAG CT C AC097634.4,FOXP1 Ensembl:ENSG00000285708,Ensembl:ENSG00000114861 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1166325885 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_219604,RMVar_hsa_circ_83199,RMVar_hsa_circ_219617,RMVar_hsa_circ_116417,RMVar_hsa_circ_267498 38036 RMVar_ID_38036 Human_SNP_ID_138344360 A-to-I Human chr3 - 71576711 71576711 71576711 CATGAAATTTACAATTCAGTTGTAATAATTTAAGGTTATTGGTAGAGTGCAAAGGGCAGTGGGAG CATGAAATTTACAATTCAGTTGTAATAATTTAGGGTTATTGGTAGAGTGCAAAGGGCAGTGGGAG T C AC097634.4,FOXP1 Ensembl:ENSG00000285708,Ensembl:ENSG00000114861 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs531803776 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17573762 RMVar_hsa_circ_219604,RMVar_hsa_circ_83199,RMVar_hsa_circ_219617,RMVar_hsa_circ_116417,RMVar_hsa_circ_267498 38037 RMVar_ID_38037 Human_SNP_ID_138361081 A-to-I Human chr3 - 71644442 71644442 71644442 GGGTTTCACCATGTTGGCCGGGCTGGTGTCGAACTCCTGACCTCAAGTGATCTGCCTGCCTCAGC GGGTTTCACCATGTTGGCCGGGCTGGTGTCGAGCTCCTGACCTCAAGTGATCTGCCTGCCTCAGC T C AC097634.4 Ensembl:ENSG00000285708 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006216214 Functional Loss SNV dbSNP153 33..33 33 - - - 38038 RMVar_ID_38038 Human_SNP_ID_138361082 A-to-I Human chr3 - 71644442 71644442 71644442 GGGTTTCACCATGTTGGCCGGGCTGGTGTCGAACTCCTGACCTCAAGTGATCTGCCTGCCTCAGC GGGTTTCACCATGTTGGCCGGGCTGGTGTCGACCTCCTGACCTCAAGTGATCTGCCTGCCTCAGC T G AC097634.4 Ensembl:ENSG00000285708 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006216214 Functional Loss SNV dbSNP153 33..33 33 - - - 38039 RMVar_ID_38039 Human_SNP_ID_138380317 A-to-I Human chr3 - 71720363 71720362 71720363 TAGCAATACCTCGTCTCTATTTTAAAAAAAAAATTAGCCGGGCATGGTGGCAAGAGCCTGTAGTC TAGCAATACCTCGTCTCTATTTTAAAAAAAAA_TTAGCCGGGCATGGTGGCAAGAGCCTGTAGTC AT A AC097634.4,EIF4E3 Ensembl:ENSG00000285708,Ensembl:ENSG00000163412 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs953563168 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_219629,RMVar_hsa_circ_321751,RMVar_hsa_circ_219630,RMVar_hsa_circ_219637,RMVar_hsa_circ_334424,RMVar_hsa_circ_219636,RMVar_hsa_circ_273305,RMVar_hsa_circ_219638 38040 RMVar_ID_38040 Human_SNP_ID_138682597 A-to-I Human chr3 + 72922999 72922999 72922999 AAATTAGGCGGGGTGTGTTGGCTTAGACCTATAATCCCAGCACTTTGGGAGGCTGAGGCGAGTGA AAATTAGGCGGGGTGTGTTGGCTTAGACCTATGATCCCAGCACTTTGGGAGGCTGAGGCGAGTGA A G GXYLT2 Ensembl:ENSG00000172986 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs575640445 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70465 38041 RMVar_ID_38041 Human_SNP_ID_138684146 A-to-I Human chr3 + 72929546 72929546 72929546 TGCAAGATGGGAGCACCCGAATCTGGCTCGGCAGAATATCTCTTTGACAAGCACACGCTGGGAGA TGCAAGATGGGAGCACCCGAATCTGGCTCGGCGGAATATCTCTTTGACAAGCACACGCTGGGAGA A G FTH1P23,GXYLT2 Ensembl:ENSG00000242960,Ensembl:ENSG00000172986 Pseudogene,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs77625415 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70465 38042 RMVar_ID_38042 Human_SNP_ID_138686221 A-to-I Human chr3 + 72938048 72938048 72938048 TGGGAGGCAGAGGTGGGAGGATGCTTGAGGCCAGGAGTTCAAGACTGGCCTGGGCAACACAGTGA TGGGAGGCAGAGGTGGGAGGATGCTTGAGGCCGGGAGTTCAAGACTGGCCTGGGCAACACAGTGA A G GXYLT2 Ensembl:ENSG00000172986 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1461907949 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70465 38043 RMVar_ID_38043 Human_SNP_ID_138690090 A-to-I Human chr3 + 72954152 72954152 72954152 TTTGAAATGGAGTCTTGCTCTGTTGCCAGGCTAGAGTGTAGTGGTGCTATCTTGGTTCACTGGAA TTTGAAATGGAGTCTTGCTCTGTTGCCAGGCTGGAGTGTAGTGGTGCTATCTTGGTTCACTGGAA A G GXYLT2 Ensembl:ENSG00000172986 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017629731 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70465 38044 RMVar_ID_38044 Human_SNP_ID_138696274 A-to-I Human chr3 + 72978073 72978073 72978073 TATGCCACATTGAATACTGGGAAGGGCCGGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTG TATGCCACATTGAATACTGGGAAGGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTG A G GXYLT2 Ensembl:ENSG00000172986 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs932237049 Functional Loss SNV dbSNP153 33..33 33 - - - 38045 RMVar_ID_38045 Human_SNP_ID_138696301 A-to-I Human chr3 + 72978135 72978135 72978135 TTGGGAGGCCGAGGCGGGCGGATCACGAGGTCAGCAGATCAAGACCATCCTTTCGAACACGGTGA TTGGGAGGCCGAGGCGGGCGGATCACGAGGTCGGCAGATCAAGACCATCCTTTCGAACACGGTGA A G GXYLT2 Ensembl:ENSG00000172986 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1289673403 Functional Loss SNV dbSNP153 33..33 33 - - - 38046 RMVar_ID_38046 Human_SNP_ID_138696305 A-to-I Human chr3 + 72978143 72978143 72978143 CCGAGGCGGGCGGATCACGAGGTCAGCAGATCAAGACCATCCTTTCGAACACGGTGAAACCCAGT CCGAGGCGGGCGGATCACGAGGTCAGCAGATCCAGACCATCCTTTCGAACACGGTGAAACCCAGT A C GXYLT2 Ensembl:ENSG00000172986 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1188879257 Functional Loss SNV dbSNP153 33..33 33 - - - 38047 RMVar_ID_38047 Human_SNP_ID_138696306 A-to-I Human chr3 + 72978143 72978143 72978143 CCGAGGCGGGCGGATCACGAGGTCAGCAGATCAAGACCATCCTTTCGAACACGGTGAAACCCAGT CCGAGGCGGGCGGATCACGAGGTCAGCAGATCGAGACCATCCTTTCGAACACGGTGAAACCCAGT A G GXYLT2 Ensembl:ENSG00000172986 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1188879257 Functional Loss SNV dbSNP153 33..33 33 - - - 38048 RMVar_ID_38048 Human_SNP_ID_138696308 A-to-I Human chr3 + 72978149 72978149 72978149 CGGGCGGATCACGAGGTCAGCAGATCAAGACCATCCTTTCGAACACGGTGAAACCCAGTATCTAC CGGGCGGATCACGAGGTCAGCAGATCAAGACCGTCCTTTCGAACACGGTGAAACCCAGTATCTAC A G GXYLT2 Ensembl:ENSG00000172986 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs186240609 Functional Loss SNV dbSNP153 33..33 33 - - - 38049 RMVar_ID_38049 Human_SNP_ID_138696329 A-to-I Human chr3 + 72978194 72978194 72978194 CGGTGAAACCCAGTATCTACTAAAAATACAAAAAATTAGCCGGGCGTGGTGGCGCCTGTGGTCCC CGGTGAAACCCAGTATCTACTAAAAATACAAAGAATTAGCCGGGCGTGGTGGCGCCTGTGGTCCC A G GXYLT2 Ensembl:ENSG00000172986 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991472155 Functional Loss SNV dbSNP153 33..33 33 - - - 38050 RMVar_ID_38050 Human_SNP_ID_138696336 A-to-I Human chr3 + 72978227 72978227 72978227 AATTAGCCGGGCGTGGTGGCGCCTGTGGTCCCAGCTACTCGCGAGGCTGAGGCAGGAGAATGGCG AATTAGCCGGGCGTGGTGGCGCCTGTGGTCCCTGCTACTCGCGAGGCTGAGGCAGGAGAATGGCG A T GXYLT2 Ensembl:ENSG00000172986 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1302659336 Functional Loss SNV dbSNP153 33..33 33 - - - 38051 RMVar_ID_38051 Human_SNP_ID_138696934 A-to-I Human chr3 + 72979931 72979931 72979931 CCTTGGCCTCCCAAAGTACTGGGACTACAGGCATGAGCCACTGTGCCCAGCTGACATATTCTCAC CCTTGGCCTCCCAAAGTACTGGGACTACAGGCGTGAGCCACTGTGCCCAGCTGACATATTCTCAC A G GXYLT2 Ensembl:ENSG00000172986 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900553017 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7225026 38052 RMVar_ID_38052 Human_SNP_ID_138702434 A-to-I Human chr3 + 73000213 73000213 73000213 TAAGTTACCTGAGTGTGTTGGTACATGCCTATAGTCCCAGCTTCTCCAGAGGCTGAGGCAGAAGG TAAGTTACCTGAGTGTGTTGGTACATGCCTATGGTCCCAGCTTCTCCAGAGGCTGAGGCAGAAGG A G PPP4R2 Ensembl:ENSG00000163605 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1009306384 Functional Loss SNV dbSNP153 33..33 33 - - - 38053 RMVar_ID_38053 Human_SNP_ID_138702737 A-to-I Human chr3 + 73001302 73001302 73001302 TTTACTGGCCAGGTGCAGTGATTCATGTCTGTAATCCCAGAACTTTGAGAGGCTGAGGCAGGTGG TTTACTGGCCAGGTGCAGTGATTCATGTCTGTGATCCCAGAACTTTGAGAGGCTGAGGCAGGTGG A G PPP4R2 Ensembl:ENSG00000163605 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1158003369 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1314469,Human_RBP_ID_14941005 38054 RMVar_ID_38054 Human_SNP_ID_138709431 A-to-I Human chr3 + 73020711 73020711 73020711 AAAAAAAAAAAAAGTTAAAAAACTTTTTTTGTAGAGACAGGGTGTTGCTGTGTTGCCCAGGCTGG AAAAAAAAAAAAAGTTAAAAAACTTTTTTTGTGGAGACAGGGTGTTGCTGTGTTGCCCAGGCTGG A G PPP4R2 Ensembl:ENSG00000163605 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1470111502 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7225327 38055 RMVar_ID_38055 Human_SNP_ID_138712643 A-to-I Human chr3 + 73030936 73030936 73030936 GTTGAGCAGGCTGGTCTCGAACTCCTGAGCTCAGGTGATCTGCCCGCCTCGGCCTCCCAAAATGC GTTGAGCAGGCTGGTCTCGAACTCCTGAGCTCGGGTGATCTGCCCGCCTCGGCCTCCCAAAATGC A G PPP4R2 Ensembl:ENSG00000163605 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs989237196 Functional Loss SNV dbSNP153 33..33 33 - - - 38056 RMVar_ID_38056 Human_SNP_ID_138718232 A-to-I Human chr3 + 73049384 73049384 73049384 AGCTGGGCGTTGTCGCGGACGCCCATAATCCCAGCTACTCGGGAGACTGAGGCAGGAAAATGGGG AGCTGGGCGTTGTCGCGGACGCCCATAATCCCGGCTACTCGGGAGACTGAGGCAGGAAAATGGGG A G PPP4R2 Ensembl:ENSG00000163605 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs549250503 Functional Loss SNV dbSNP153 33..33 33 - - - 38057 RMVar_ID_38057 Human_SNP_ID_138719753 A-to-I Human chr3 + 73054192 73054192 73054192 CACCCGCCTCGGTCCCCCAAAATGCTGGGATTACAGGCGTGAGCCGCCGTGCTCAGCTAATTTCG CACCCGCCTCGGTCCCCCAAAATGCTGGGATTGCAGGCGTGAGCCGCCGTGCTCAGCTAATTTCG A G PPP4R2 Ensembl:ENSG00000163605 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs965884306 Functional Loss SNV dbSNP153 33..33 33 - - - 38058 RMVar_ID_38058 Human_SNP_ID_138723894 A-to-I Human chr3 + 73066441 73066441 73066441 TGAAACCCTGGAAATCTTAAGTCTGTTGAAATACCAGGTTAAACACATTCCAAGAGATCTGTTCA TGAAACCCTGGAAATCTTAAGTCTGTTGAAATGCCAGGTTAAACACATTCCAAGAGATCTGTTCA A G PPP4R2 Ensembl:ENSG00000163605 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1398425862 Functional Loss SNV dbSNP153 33..33 33 - - - 38059 RMVar_ID_38059 Human_SNP_ID_690429016 A-to-I Human chr21 + 21024842 21024842 21024842 CCAGGAGGCGGAGACTGCAGTGAGCTGAGATCACACCACTTCACTCCAGCCTGGGCCAGAGAGGG CCAGGAGGCGGAGACTGCAGTGAGCTGAGATCGCACCACTTCACTCCAGCCTGGGCCAGAGAGGG A G NCAM2 Ensembl:ENSG00000154654 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1352266501 Functional Loss SNV dbSNP153 33..33 33 - - - 38060 RMVar_ID_38060 Human_SNP_ID_690430390 A-to-I Human chr21 + 21029772 21029772 21029772 CCTGCCTTAGCCTCCCGAGTAGCTGGGGCTGCAAGTGCACACCGCCATGCCCAGCTAATTTTTTG CCTGCCTTAGCCTCCCGAGTAGCTGGGGCTGCCAGTGCACACCGCCATGCCCAGCTAATTTTTTG A C NCAM2 Ensembl:ENSG00000154654 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs898155393 Functional Loss SNV dbSNP153 33..33 33 - - - 38061 RMVar_ID_38061 Human_SNP_ID_690439322 A-to-I Human chr21 + 21063386 21063386 21063386 GGGTCTACAGGCATGCGCCAGCACGCCTGGCTAATTTTTGTATTTTTAGTAGAGATGGAGTTTCA GGGTCTACAGGCATGCGCCAGCACGCCTGGCTCATTTTTGTATTTTTAGTAGAGATGGAGTTTCA A C NCAM2 Ensembl:ENSG00000154654 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1211913436 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_211552 38062 RMVar_ID_38062 Human_SNP_ID_690443909 A-to-I Human chr21 + 21080388 21080387 21080388 CCTGTAATCCCAGCATTTTGGGAGGCCGAGGTAGGCAGGTCACCTGAGGTAGGGAGTTCAGGACC CCTGTAATCCCAGCATTTTGGGAGGCCGAGGT_GGCAGGTCACCTGAGGTAGGGAGTTCAGGACC TA T NCAM2 Ensembl:ENSG00000154654 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1248946465 Functional Loss DEL dbSNP153 33..33 33 - - - 38063 RMVar_ID_38063 Human_SNP_ID_690443922 A-to-I Human chr21 + 21080430 21080430 21080430 CCTGAGGTAGGGAGTTCAGGACCAGCCTGACCAACATGGAGAAACCCCATCTCCACTAAAAATAC CCTGAGGTAGGGAGTTCAGGACCAGCCTGACCGACATGGAGAAACCCCATCTCCACTAAAAATAC A G NCAM2 Ensembl:ENSG00000154654 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs943478795 Functional Loss SNV dbSNP153 33..33 33 - - - 38064 RMVar_ID_38064 Human_SNP_ID_690444498 A-to-I Human chr21 + 21082044 21082043 21082047 TGGATCAGGAGTTCGAGACCAGCCTGACCAACAAGATGAAACCCCATCTCTACTAAAAATACAAA TGGATCAGGAGTTCGAGACCAGCCTGACCAATAAGGTGAAACCCCATCTCTACTAAAAATACAAA CAAGA TAAGG NCAM2 Ensembl:ENSG00000154654 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs386817026 Functional Loss MNV dbSNP153 32..36 33 - - - 38065 RMVar_ID_38065 Human_SNP_ID_690451776 A-to-I Human chr21 + 21110510 21110510 21110510 TAGGGGACACTGGGGACTCTACATATAAAGATACAATTTCCTCTGTGTTTAATAAAGTCTAGGGT TAGGGGACACTGGGGACTCTACATATAAAGATTCAATTTCCTCTGTGTTTAATAAAGTCTAGGGT A T NCAM2 Ensembl:ENSG00000154654 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1334610534 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_211553 38066 RMVar_ID_38066 Human_SNP_ID_690490528 A-to-I Human chr21 + 21257699 21257699 21257699 CTGCCTCCCGGGTTGAAGCAATTCTCCTGCCTAAACCTCCTGAGTAGCTGGGGTTCCAGGGACCC CTGCCTCCCGGGTTGAAGCAATTCTCCTGCCTGAACCTCCTGAGTAGCTGGGGTTCCAGGGACCC A G NCAM2 Ensembl:ENSG00000154654 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1481765581 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42190,RMVar_hsa_circ_331148 38067 RMVar_ID_38067 Human_SNP_ID_690490548 A-to-I Human chr21 + 21257772 21257772 21257772 GCCTGGCTACTTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAAGCTGCTCTCAA GCCTGGCTACTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAAGCTGCTCTCAA A G NCAM2 Ensembl:ENSG00000154654 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs887623139 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42190,RMVar_hsa_circ_331148 38068 RMVar_ID_38068 Human_SNP_ID_691654243 A-to-I Human chr21 - 25606337 25606337 25606337 GTAATTACTTCTGGTCATCTGTGGCCATGGCAATCCCTTTATACCAAAATCCTTTCTTGAGACCT GTAATTACTTCTGGTCATCTGTGGCCATGGCAGTCCCTTTATACCAAAATCCTTTCTTGAGACCT T C MRPL39 Ensembl:ENSG00000154719 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1237581555 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_375730,RMVar_hsa_circ_211592 38069 RMVar_ID_38069 Human_SNP_ID_691680959 A-to-I Human chr21 - 25721056 25721056 25721056 CACCCATGCTGTTCTCGAACTTCTAGATTCCAATGATCCTCCCACCTCAGCCTCCCAAAGTGCTG CACCCATGCTGTTCTCGAACTTCTAGATTCCAGTGATCCTCCCACCTCAGCCTCCCAAAGTGCTG T C ATP5PF Ensembl:ENSG00000154723 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1305862363 Functional Loss SNV dbSNP153 33..33 33 - - - 38070 RMVar_ID_38070 Human_SNP_ID_691684647 A-to-I Human chr21 - 25735231 25735231 25735231 TCCCTGCACCTTTATACACTTCGATAACCCTAACGAACAGGACGCTGACTCGGAGGGGAGCTTGA TCCCTGCACCTTTATACACTTCGATAACCCTACCGAACAGGACGCTGACTCGGAGGGGAGCTTGA T G ATP5PF Ensembl:ENSG00000154723 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1481291619 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4666623,Human_RBP_ID_22423041 38071 RMVar_ID_38071 Human_SNP_ID_691684650 A-to-I Human chr21 - 25735238 25735238 25735238 CTCACTTTCCCTGCACCTTTATACACTTCGATAACCCTAACGAACAGGACGCTGACTCGGAGGGG CTCACTTTCCCTGCACCTTTATACACTTCGATTACCCTAACGAACAGGACGCTGACTCGGAGGGG T A ATP5PF Ensembl:ENSG00000154723 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs71649643 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4666625,Human_RBP_ID_22423041 38072 RMVar_ID_38072 Human_SNP_ID_691684651 A-to-I Human chr21 - 25735238 25735238 25735238 CTCACTTTCCCTGCACCTTTATACACTTCGATAACCCTAACGAACAGGACGCTGACTCGGAGGGG CTCACTTTCCCTGCACCTTTATACACTTCGATCACCCTAACGAACAGGACGCTGACTCGGAGGGG T G ATP5PF Ensembl:ENSG00000154723 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs71649643 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4666625,Human_RBP_ID_22423041 38073 RMVar_ID_38073 Human_SNP_ID_691685930 A-to-I Human chr21 + 25739886 25739886 25739886 ACAGTCCTCTCTCCTCGATCTCCCAGAGTATTAGGATTACAGGCATGAGGCACCGTATCTGGCCC ACAGTCCTCTCTCCTCGATCTCCCAGAGTATTTGGATTACAGGCATGAGGCACCGTATCTGGCCC A T GABPA Ensembl:ENSG00000154727 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs571974259 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7031428,Human_RBP_ID_14209881 38074 RMVar_ID_38074 Human_SNP_ID_691738260 A-to-I Human chr21 - 25909187 25909187 25909187 GCGATCTCAGCTCACTGCAAACTCTGCCTCCCAGGTTCATGCCATTTTCTTGCTTCAGCCTCCCG GCGATCTCAGCTCACTGCAAACTCTGCCTCCCGGGTTCATGCCATTTTCTTGCTTCAGCCTCCCG T C APP Ensembl:ENSG00000142192 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1486832266 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_53034,RMVar_hsa_circ_30326,RMVar_hsa_circ_72605,RMVar_hsa_circ_272752,RMVar_hsa_circ_40016,RMVar_hsa_circ_24530,RMVar_hsa_circ_62100,RMVar_hsa_circ_211607,RMVar_hsa_circ_298707,RMVar_hsa_circ_211608,RMVar_hsa_circ_31488,RMVar_hsa_circ_333892 38075 RMVar_ID_38075 Human_SNP_ID_691763158 A-to-I Human chr21 - 26005231 26005231 26005231 TTTTGTATTTTTAGTAGAGACAGGGTTTCGCCATGTTGACTACGTTGGTCTTGAACTCCTGACCT TTTTGTATTTTTAGTAGAGACAGGGTTTCGCCGTGTTGACTACGTTGGTCTTGAACTCCTGACCT T C APP Ensembl:ENSG00000142192 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025025384 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72605,RMVar_hsa_circ_20814,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_43543,RMVar_hsa_circ_57301,RMVar_hsa_circ_73432 38076 RMVar_ID_38076 Human_SNP_ID_691764555 A-to-I Human chr21 - 26010644 26010644 26010644 GCTAATATATTTTTTTTTTTTGTAGTTTTAGTAGAGACAGGGTTTCACCATGTTAGCCAGGCTGA GCTAATATATTTTTTTTTTTTGTAGTTTTAGTGGAGACAGGGTTTCACCATGTTAGCCAGGCTGA T C APP Ensembl:ENSG00000142192 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1241281260 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72605,RMVar_hsa_circ_20814,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_43543,RMVar_hsa_circ_57301,RMVar_hsa_circ_73432 38077 RMVar_ID_38077 Human_SNP_ID_691801300 A-to-I Human chr21 - 26155103 26155103 26155103 GGGATTACAGGCGTGTGCCATCACACCCAGCTAATTTTTTTATTTTTGGTAGGGATGAGATTTCA GGGATTACAGGCGTGTGCCATCACACCCAGCTTATTTTTTTATTTTTGGTAGGGATGAGATTTCA T A APP Ensembl:ENSG00000142192 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1164846438 Functional Loss SNV dbSNP153 33..33 33 - - - 38078 RMVar_ID_38078 Human_SNP_ID_691881198 A-to-I Human chr21 - 26479709 26479709 26479709 GCAAGGGTTCATGACTAGCCTGGCCAACTTGGAGAAACTCAGTCTCTACTAAAAATACAAAAGAA GCAAGGGTTCATGACTAGCCTGGCCAACTTGGCGAAACTCAGTCTCTACTAAAAATACAAAAGAA T G CYYR1 Ensembl:ENSG00000166265 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1321132070 Functional Loss SNV dbSNP153 33..33 33 - - - 38079 RMVar_ID_38079 Human_SNP_ID_692514678 A-to-I Human chr21 + 29028395 29028395 29028395 GTGATCCGCCTGCCTTGGCCTCCAAAAGTGCTAGGATTACACGTGAGAGCCACTGCACCTGACTT GTGATCCGCCTGCCTTGGCCTCCAAAAGTGCTGGGATTACACGTGAGAGCCACTGCACCTGACTT A G USP16 Ensembl:ENSG00000156256 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1368993408 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14222456 RMVar_hsa_circ_12482,RMVar_hsa_circ_312965,RMVar_hsa_circ_353590,RMVar_hsa_circ_361454,RMVar_hsa_circ_362700,RMVar_hsa_circ_363615,RMVar_hsa_circ_354831,RMVar_hsa_circ_335105,RMVar_hsa_circ_68386,RMVar_hsa_circ_70161,RMVar_hsa_circ_211650,RMVar_hsa_circ_9814 38080 RMVar_ID_38080 Human_SNP_ID_692514750 A-to-I Human chr21 + 29028695 29028695 29028695 TGACCTCAAGTGATCCGCTTCCTCAGCATCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCG TGACCTCAAGTGATCCGCTTCCTCAGCATCCCGAAGTGCTGGGATTACAGGCGTGAGCCACCGCG A G USP16 Ensembl:ENSG00000156256 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs182691085 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12482,RMVar_hsa_circ_312965,RMVar_hsa_circ_353590,RMVar_hsa_circ_361454,RMVar_hsa_circ_362700,RMVar_hsa_circ_363615,RMVar_hsa_circ_354831,RMVar_hsa_circ_335105,RMVar_hsa_circ_68386,RMVar_hsa_circ_70161,RMVar_hsa_circ_211650,RMVar_hsa_circ_9814 38081 RMVar_ID_38081 Human_SNP_ID_692521597 A-to-I Human chr21 + 29055419 29055419 29055419 AAAAACAGGCTGGTGCGGTGGCTTATGCTTGTAATCCCAGGACTCTGGGAGGTCAAGGCAGTAGG AAAAACAGGCTGGTGCGGTGGCTTATGCTTGTGATCCCAGGACTCTGGGAGGTCAAGGCAGTAGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1362710090 Functional Loss SNV dbSNP153 33..33 33 - - - 38082 RMVar_ID_38082 Human_SNP_ID_692522167 A-to-I Human chr21 - 29057444 29057444 29057444 AAGATGTTTTCCAGCCGAGCGCAGTGGCTCACACCTATAATCCCAACACTTTGGGAGGCTGAGGC AAGATGTTTTCCAGCCGAGCGCAGTGGCTCACCCCTATAATCCCAACACTTTGGGAGGCTGAGGC T G CCT8 Ensembl:ENSG00000156261 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1484741793 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76958,RMVar_hsa_circ_105696,RMVar_hsa_circ_124657,RMVar_hsa_circ_113837,RMVar_hsa_circ_115761,RMVar_hsa_circ_83035,RMVar_hsa_circ_97611,RMVar_hsa_circ_80156,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_211655 38083 RMVar_ID_38083 Human_SNP_ID_692522476 A-to-I Human chr21 - 29058000 29058000 29058000 TTTTTGTTGTTGTTGTGATAAGGTCTTACTCTATCACCCAGGCTGGAGGACAGTGGCACAATCAT TTTTTGTTGTTGTTGTGATAAGGTCTTACTCTGTCACCCAGGCTGGAGGACAGTGGCACAATCAT T C CCT8 Ensembl:ENSG00000156261 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs928020389 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14223986,Human_RBP_ID_17572402 RMVar_hsa_circ_76958,RMVar_hsa_circ_105696,RMVar_hsa_circ_124657,RMVar_hsa_circ_113837,RMVar_hsa_circ_115761,RMVar_hsa_circ_83035,RMVar_hsa_circ_97611,RMVar_hsa_circ_80156,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_211655 38084 RMVar_ID_38084 Human_SNP_ID_692522574 A-to-I Human chr21 - 29058378 29058378 29058378 GGAGTGCAGTGGTGTGATCTCAGCTTACTGCAACCGCCACCTCCCAGGTTCAAGCAATTCTGCTG GGAGTGCAGTGGTGTGATCTCAGCTTACTGCATCCGCCACCTCCCAGGTTCAAGCAATTCTGCTG T A CCT8,AF129075.2 Ensembl:ENSG00000156261,Ensembl:ENSG00000231125 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs977950844 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76958,RMVar_hsa_circ_105696,RMVar_hsa_circ_124657,RMVar_hsa_circ_113837,RMVar_hsa_circ_115761,RMVar_hsa_circ_83035,RMVar_hsa_circ_97611,RMVar_hsa_circ_80156,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_211655 38085 RMVar_ID_38085 Human_SNP_ID_692522575 A-to-I Human chr21 - 29058378 29058378 29058378 GGAGTGCAGTGGTGTGATCTCAGCTTACTGCAACCGCCACCTCCCAGGTTCAAGCAATTCTGCTG GGAGTGCAGTGGTGTGATCTCAGCTTACTGCAGCCGCCACCTCCCAGGTTCAAGCAATTCTGCTG T C CCT8,AF129075.2 Ensembl:ENSG00000156261,Ensembl:ENSG00000231125 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs977950844 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76958,RMVar_hsa_circ_105696,RMVar_hsa_circ_124657,RMVar_hsa_circ_113837,RMVar_hsa_circ_115761,RMVar_hsa_circ_83035,RMVar_hsa_circ_97611,RMVar_hsa_circ_80156,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_211655 38086 RMVar_ID_38086 Human_SNP_ID_692522576 A-to-I Human chr21 - 29058378 29058378 29058378 GGAGTGCAGTGGTGTGATCTCAGCTTACTGCAACCGCCACCTCCCAGGTTCAAGCAATTCTGCTG GGAGTGCAGTGGTGTGATCTCAGCTTACTGCACCCGCCACCTCCCAGGTTCAAGCAATTCTGCTG T G CCT8,AF129075.2 Ensembl:ENSG00000156261,Ensembl:ENSG00000231125 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs977950844 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76958,RMVar_hsa_circ_105696,RMVar_hsa_circ_124657,RMVar_hsa_circ_113837,RMVar_hsa_circ_115761,RMVar_hsa_circ_83035,RMVar_hsa_circ_97611,RMVar_hsa_circ_80156,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_211655 38087 RMVar_ID_38087 Human_SNP_ID_692524152 A-to-I Human chr21 - 29064045 29064045 29064045 TAAAATAAAAGCACTTCTCGGCCGGGCACGGTATCTCACGCCTGTAATCCCAGCATAGGCCAAGG TAAAATAAAAGCACTTCTCGGCCGGGCACGGTTTCTCACGCCTGTAATCCCAGCATAGGCCAAGG T A CCT8 Ensembl:ENSG00000156261 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1055786560 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14224312 RMVar_hsa_circ_105696,RMVar_hsa_circ_124657,RMVar_hsa_circ_113837,RMVar_hsa_circ_83035,RMVar_hsa_circ_97611,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_28303,RMVar_hsa_circ_326873,RMVar_hsa_circ_17222,RMVar_hsa_circ_211663,RMVar_hsa_circ_88909,RMVar_hsa_circ_35494,RMVar_hsa_circ_211664,RMVar_hsa_circ_76556,RMVar_hsa_circ_211666,RMVar_hsa_circ_30217,RMVar_hsa_circ_358699,RMVar_hsa_circ_211667,RMVar_hsa_circ_311509 38088 RMVar_ID_38088 Human_SNP_ID_692524198 A-to-I Human chr21 - 29064203 29064203 29064203 CCTTGGCCTCCCAGAGTGCTAGGATTACAGGCATGAGCCACCGCGCCCGGCCTAGTCCACATTTT CCTTGGCCTCCCAGAGTGCTAGGATTACAGGCGTGAGCCACCGCGCCCGGCCTAGTCCACATTTT T C CCT8 Ensembl:ENSG00000156261 Protein coding intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1341787322 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105696,RMVar_hsa_circ_124657,RMVar_hsa_circ_113837,RMVar_hsa_circ_83035,RMVar_hsa_circ_97611,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_28303,RMVar_hsa_circ_326873,RMVar_hsa_circ_17222,RMVar_hsa_circ_211663,RMVar_hsa_circ_88909,RMVar_hsa_circ_35494,RMVar_hsa_circ_211664,RMVar_hsa_circ_76556,RMVar_hsa_circ_211666,RMVar_hsa_circ_30217,RMVar_hsa_circ_358699,RMVar_hsa_circ_211667,RMVar_hsa_circ_311509 38089 RMVar_ID_38089 Human_SNP_ID_692524211 A-to-I Human chr21 - 29064261 29064261 29064261 AAGTTTCACCATGTTGGCCAGACTGGTCTCCAACTCCTGACTGCAAGTGATCCACCCGCCTTGGC AAGTTTCACCATGTTGGCCAGACTGGTCTCCAGCTCCTGACTGCAAGTGATCCACCCGCCTTGGC T C CCT8 Ensembl:ENSG00000156261 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1372655586 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14224322 RMVar_hsa_circ_105696,RMVar_hsa_circ_124657,RMVar_hsa_circ_113837,RMVar_hsa_circ_83035,RMVar_hsa_circ_97611,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_28303,RMVar_hsa_circ_326873,RMVar_hsa_circ_17222,RMVar_hsa_circ_211663,RMVar_hsa_circ_88909,RMVar_hsa_circ_35494,RMVar_hsa_circ_211664,RMVar_hsa_circ_76556,RMVar_hsa_circ_211666,RMVar_hsa_circ_30217,RMVar_hsa_circ_358699,RMVar_hsa_circ_211667,RMVar_hsa_circ_311509 38090 RMVar_ID_38090 Human_SNP_ID_692524217 A-to-I Human chr21 - 29064302 29064302 29064302 CAAGTGATCTCTGGCTAATTTTTGTATTTTTAATAGAGACAAAGTTTCACCATGTTGGCCAGACT CAAGTGATCTCTGGCTAATTTTTGTATTTTTATTAGAGACAAAGTTTCACCATGTTGGCCAGACT T A CCT8 Ensembl:ENSG00000156261 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs990408393 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14224325 RMVar_hsa_circ_105696,RMVar_hsa_circ_124657,RMVar_hsa_circ_113837,RMVar_hsa_circ_83035,RMVar_hsa_circ_97611,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_28303,RMVar_hsa_circ_326873,RMVar_hsa_circ_17222,RMVar_hsa_circ_211663,RMVar_hsa_circ_88909,RMVar_hsa_circ_35494,RMVar_hsa_circ_211664,RMVar_hsa_circ_76556,RMVar_hsa_circ_211666,RMVar_hsa_circ_30217,RMVar_hsa_circ_358699,RMVar_hsa_circ_211667,RMVar_hsa_circ_311509 38091 RMVar_ID_38091 Human_SNP_ID_692524226 A-to-I Human chr21 - 29064352 29064352 29064352 TGAGTCCAGTGGTACAATCTTGGCTCCCTGCAACCTCCGCCTCCTGGGTTCAAGTGATCTCTGGC TGAGTCCAGTGGTACAATCTTGGCTCCCTGCAGCCTCCGCCTCCTGGGTTCAAGTGATCTCTGGC T C CCT8 Ensembl:ENSG00000156261 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432628785 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105696,RMVar_hsa_circ_124657,RMVar_hsa_circ_113837,RMVar_hsa_circ_83035,RMVar_hsa_circ_97611,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_28303,RMVar_hsa_circ_326873,RMVar_hsa_circ_17222,RMVar_hsa_circ_211663,RMVar_hsa_circ_88909,RMVar_hsa_circ_35494,RMVar_hsa_circ_211664,RMVar_hsa_circ_76556,RMVar_hsa_circ_211666,RMVar_hsa_circ_30217,RMVar_hsa_circ_358699,RMVar_hsa_circ_211667,RMVar_hsa_circ_311509 38092 RMVar_ID_38092 Human_SNP_ID_692590649 A-to-I Human chr21 + 29353032 29353032 29353032 ACTGTGTCCAGCCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACTATGTTTGCCAGGCTGG ACTGTGTCCAGCCTAATTTTTGTATTTTTAGTGGAGATGGGGTTTCACTATGTTTGCCAGGCTGG A G BACH1,BACH1-IT1 Ensembl:ENSG00000156273,Ensembl:ENSG00000248476 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs758384442 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76256,RMVar_hsa_circ_378831,RMVar_hsa_circ_211681,RMVar_hsa_circ_211686,RMVar_hsa_circ_211695 38093 RMVar_ID_38093 Human_SNP_ID_692602918 A-to-I Human chr21 + 29405901 29405901 29405901 TTGCCCAGGCACAATCACAGTGGCACAATCACAGCTCACTGATCCTTGACCTCCTTGGCCCAAGC TTGCCCAGGCACAATCACAGTGGCACAATCACTGCTCACTGATCCTTGACCTCCTTGGCCCAAGC A T BACH1 Ensembl:ENSG00000156273 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1353987740 Functional Loss SNV dbSNP153 33..33 33 - - - 38094 RMVar_ID_38094 Human_SNP_ID_692612740 A-to-I Human chr21 + 29447207 29447203 29447208 AAGACAAAGACCAGCTGGGTGCCATGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGT AAGACAAAGACCAGCTGGGTGCCATGGCT_____CTGTAATCCCAGCACTTTGGGAGGCCAAGGT TCACAC T BACH1 Ensembl:ENSG00000156273 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs200513869 Functional Loss DEL dbSNP153 30..34 33 - - - 38095 RMVar_ID_38095 Human_SNP_ID_692612743 A-to-I Human chr21 + 29447207 29447207 29447207 AAGACAAAGACCAGCTGGGTGCCATGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGT AAGACAAAGACCAGCTGGGTGCCATGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGT A G BACH1 Ensembl:ENSG00000156273 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs912681920 Functional Loss SNV dbSNP153 33..33 33 - - - 38096 RMVar_ID_38096 Human_SNP_ID_693035077 A-to-I Human chr21 - 31134005 31134005 31134005 GGAGTGCAATGGTGCGTTCTCGGCTCACTGCAACCTCTGCCTCCCAGGTTCAAGCGATTGTCCTG GGAGTGCAATGGTGCGTTCTCGGCTCACTGCAGCCTCTGCCTCCCAGGTTCAAGCGATTGTCCTG T C TIAM1 Ensembl:ENSG00000156299 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1006480973 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15073,RMVar_hsa_circ_65855,RMVar_hsa_circ_266440,RMVar_hsa_circ_47839,RMVar_hsa_circ_11505,RMVar_hsa_circ_374759,RMVar_hsa_circ_211704 38097 RMVar_ID_38097 Human_SNP_ID_693037042 A-to-I Human chr21 - 31142400 31142400 31142400 TTGGCCAGGCTGCTTTCAAACTCCTGACCTCAAGTGATCCGCTCGCCTCTGCCTCCCAAACTGCT TTGGCCAGGCTGCTTTCAAACTCCTGACCTCAGGTGATCCGCTCGCCTCTGCCTCCCAAACTGCT T C TIAM1 Ensembl:ENSG00000156299 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1044791292 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15073,RMVar_hsa_circ_65855,RMVar_hsa_circ_266440,RMVar_hsa_circ_47839,RMVar_hsa_circ_59467 38098 RMVar_ID_38098 Human_SNP_ID_693044969 A-to-I Human chr21 - 31172836 31172836 31172836 TAGAGTTGGGGTTTCTCTCTGTCACCCATGCTAGAGTGCAGTGTCACAATCATGGTTCACTGCAG TAGAGTTGGGGTTTCTCTCTGTCACCCATGCTGGAGTGCAGTGTCACAATCATGGTTCACTGCAG T C TIAM1 Ensembl:ENSG00000156299 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1353550174 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_865,RMVar_hsa_circ_65855,RMVar_hsa_circ_47839,RMVar_hsa_circ_17084,RMVar_hsa_circ_46931,RMVar_hsa_circ_59467,RMVar_hsa_circ_73797,RMVar_hsa_circ_354160,RMVar_hsa_circ_362424,RMVar_hsa_circ_338644,RMVar_hsa_circ_23903,RMVar_hsa_circ_326679,RMVar_hsa_circ_364165,RMVar_hsa_circ_355372,RMVar_hsa_circ_275879,RMVar_hsa_circ_309327 38099 RMVar_ID_38099 Human_SNP_ID_693075259 A-to-I Human chr21 - 31291625 31291625 31291625 CCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCTGGGAGTGGAGGTTGCAGTGAGCC CCAGCTACTCAGGAGGCTGAGGCAGGAGAATCTCTTGAACCTGGGAGTGGAGGTTGCAGTGAGCC T A TIAM1 Ensembl:ENSG00000156299 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs572110421 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_65855,RMVar_hsa_circ_59467,RMVar_hsa_circ_73797,RMVar_hsa_circ_369084,RMVar_hsa_circ_64821,RMVar_hsa_circ_368860,RMVar_hsa_circ_364642,RMVar_hsa_circ_310831,RMVar_hsa_circ_55824,RMVar_hsa_circ_300950,RMVar_hsa_circ_340415 38100 RMVar_ID_38100 Human_SNP_ID_693085744 A-to-I Human chr21 - 31332969 31332969 31332969 TCAGCCTCCTGAGTGGCTGGGACTGCAGTCATACATCACCATGCCTGGTTTATTTAGTTCTTTTT TCAGCCTCCTGAGTGGCTGGGACTGCAGTCATGCATCACCATGCCTGGTTTATTTAGTTCTTTTT T C TIAM1 Ensembl:ENSG00000156299 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs997968317 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_65855,RMVar_hsa_circ_59467,RMVar_hsa_circ_73797,RMVar_hsa_circ_369084,RMVar_hsa_circ_64821,RMVar_hsa_circ_368860,RMVar_hsa_circ_364642,RMVar_hsa_circ_310831,RMVar_hsa_circ_55824,RMVar_hsa_circ_300950,RMVar_hsa_circ_340415 38101 RMVar_ID_38101 Human_SNP_ID_693170823 A-to-I Human chr21 + 31661623 31661623 31661623 TGACGTCGTGATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCCCGC TGACGTCGTGATCCACCCGCCTCGGCCTCCCAGAGTGCTGGGATTACAGGCGTGAGCCACCCCGC A G SOD1 Ensembl:ENSG00000142168 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1008287203 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83724,RMVar_hsa_circ_211722 38102 RMVar_ID_38102 Human_SNP_ID_693178902 A-to-I Human chr21 - 31689826 31689826 31689826 GGTTCCAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCGCGTGCCACCGTGC GGTTCCAGTGATTCTCCTGCCTCAGCCTCCCAGGTAGCTGGGACTACAGGCGCGTGCCACCGTGC T C SCAF4 Ensembl:ENSG00000156304 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1300749516 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25070,RMVar_hsa_circ_307880,RMVar_hsa_circ_359427,RMVar_hsa_circ_372592,RMVar_hsa_circ_308655,RMVar_hsa_circ_286862,RMVar_hsa_circ_65140,RMVar_hsa_circ_58772,RMVar_hsa_circ_124608,RMVar_hsa_circ_211725,RMVar_hsa_circ_211727,RMVar_hsa_circ_211728,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_66377,RMVar_hsa_circ_329754,RMVar_hsa_circ_211735,RMVar_hsa_circ_14147,RMVar_hsa_circ_211734 38103 RMVar_ID_38103 Human_SNP_ID_693188083 A-to-I Human chr21 - 31722790 31722790 31722790 TGCCACCACACCCGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCTCAATGTTGGCCAGGC TGCCACCACACCCGGCTAATTTTTGTATTTTTCGTAGAGACGGGGTTTCTCAATGTTGGCCAGGC T G SCAF4 Ensembl:ENSG00000156304 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924517351 Functional Loss SNV dbSNP153 33..33 33 - - - 38104 RMVar_ID_38104 Human_SNP_ID_693189486 A-to-I Human chr21 - 31727216 31727216 31727216 AAATTAGCTGGGCCTGGTGGTAGGCGCCTGTAATCCCAGCTACTTGGGAGGCTGAAGTAGGAGAA AAATTAGCTGGGCCTGGTGGTAGGCGCCTGTACTCCCAGCTACTTGGGAGGCTGAAGTAGGAGAA T G SCAF4 Ensembl:ENSG00000156304 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1376020840 Functional Loss SNV dbSNP153 33..33 33 - - - 38105 RMVar_ID_38105 Human_SNP_ID_693324184 A-to-I Human chr21 - 32285170 32285170 32285170 GGGAGGTCGAGGTGGGCGGATTGCCTGAGGTCAGGAGTTCGAGATTAGTCTGGCCAACATGGTGA GGGAGGTCGAGGTGGGCGGATTGCCTGAGGTCGGGAGTTCGAGATTAGTCTGGCCAACATGGTGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1241130765 Functional Loss SNV dbSNP153 33..33 33 - - - 38106 RMVar_ID_38106 Human_SNP_ID_693343544 A-to-I Human chr21 - 32355757 32355757 32355757 AAAAATTAGAAAAATTAGCTGGACGTGTTGGCACACTCCTGTAGTCCCAGCTACTCAGGAGGCCA AAAAATTAGAAAAATTAGCTGGACGTGTTGGCGCACTCCTGTAGTCCCAGCTACTCAGGAGGCCA T C URB1 Ensembl:ENSG00000142207 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1184898164 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3629,RMVar_hsa_circ_42786,RMVar_hsa_circ_78541,RMVar_hsa_circ_269601,RMVar_hsa_circ_211747,RMVar_hsa_circ_211749,RMVar_hsa_circ_110931,RMVar_hsa_circ_112366,RMVar_hsa_circ_116228,RMVar_hsa_circ_211752,RMVar_hsa_circ_373899,RMVar_hsa_circ_266569,RMVar_hsa_circ_88450,RMVar_hsa_circ_95485,RMVar_hsa_circ_211753,RMVar_hsa_circ_211755,RMVar_hsa_circ_211754,RMVar_hsa_circ_105742,RMVar_hsa_circ_211758,RMVar_hsa_circ_127539,RMVar_hsa_circ_211760,RMVar_hsa_circ_211761,RMVar_hsa_circ_48979,RMVar_hsa_circ_79639,RMVar_hsa_circ_372329,RMVar_hsa_circ_211765,RMVar_hsa_circ_211766,RMVar_hsa_circ_104718,RMVar_hsa_circ_99181,RMVar_hsa_circ_115211,RMVar_hsa_circ_211767,RMVar_hsa_circ_51429,RMVar_hsa_circ_30965,RMVar_hsa_circ_211768,RMVar_hsa_circ_23400,RMVar_hsa_circ_211769,RMVar_hsa_circ_106261,RMVar_hsa_circ_95349,RMVar_hsa_circ_211771,RMVar_hsa_circ_211772 38107 RMVar_ID_38107 Human_SNP_ID_693346109 A-to-I Human chr21 - 32365368 32365368 32365368 TAGCTCATTGCAGCGTCAAACTCTTGGACCCAAGTGTTCCTCACACCTCAGCCCCCTGAGTAGCT TAGCTCATTGCAGCGTCAAACTCTTGGACCCAGGTGTTCCTCACACCTCAGCCCCCTGAGTAGCT T C URB1 Ensembl:ENSG00000142207 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1190329961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14245848 RMVar_hsa_circ_3629,RMVar_hsa_circ_42786,RMVar_hsa_circ_78541,RMVar_hsa_circ_269601,RMVar_hsa_circ_211747,RMVar_hsa_circ_211749,RMVar_hsa_circ_110931,RMVar_hsa_circ_112366,RMVar_hsa_circ_116228,RMVar_hsa_circ_211752,RMVar_hsa_circ_266569,RMVar_hsa_circ_88450,RMVar_hsa_circ_211753,RMVar_hsa_circ_211754,RMVar_hsa_circ_105742,RMVar_hsa_circ_127539,RMVar_hsa_circ_211760,RMVar_hsa_circ_211761,RMVar_hsa_circ_48979,RMVar_hsa_circ_79639,RMVar_hsa_circ_372329,RMVar_hsa_circ_211765,RMVar_hsa_circ_211766,RMVar_hsa_circ_99181,RMVar_hsa_circ_115211,RMVar_hsa_circ_32928,RMVar_hsa_circ_30965,RMVar_hsa_circ_211768,RMVar_hsa_circ_211769,RMVar_hsa_circ_95349,RMVar_hsa_circ_211772,RMVar_hsa_circ_46818,RMVar_hsa_circ_85046,RMVar_hsa_circ_211775,RMVar_hsa_circ_57510,RMVar_hsa_circ_361242 38108 RMVar_ID_38108 Human_SNP_ID_693363753 A-to-I Human chr21 + 32436264 32436264 32436264 TTTTGTATTTTTAATAGAGACGGGGTTTCGCCATGTTGGCCAGGCTGTTCTCGAACTCCTCACCT TTTTGTATTTTTAATAGAGACGGGGTTTCGCCGTGTTGGCCAGGCTGTTCTCGAACTCCTCACCT A G EVA1C Ensembl:ENSG00000166979 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1308583771 Functional Loss SNV dbSNP153 33..33 33 - - - 38109 RMVar_ID_38109 Human_SNP_ID_693364262 A-to-I Human chr21 + 32438235 32438235 32438235 TAAGAGAACCCTGGCTGGGCATGGTGGCTTACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGC TAAGAGAACCCTGGCTGGGCATGGTGGCTTACCCCTGTAATCCCAGCACTTTGGGAGGCCAAGGC A C EVA1C Ensembl:ENSG00000166979 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1171533003 Functional Loss SNV dbSNP153 33..33 33 - - - 38110 RMVar_ID_38110 Human_SNP_ID_693367896 A-to-I Human chr21 + 32454052 32454052 32454052 GGAGTTCAAGACCAGCCTGGCCAATATGGTGAAACCCCATCTCTACTAATAATACAAAAATTAGC GGAGTTCAAGACCAGCCTGGCCAATATGGTGACACCCCATCTCTACTAATAATACAAAAATTAGC A C EVA1C Ensembl:ENSG00000166979 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1385683161 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_272160,RMVar_hsa_circ_319359,RMVar_hsa_circ_75137,RMVar_hsa_circ_271950,RMVar_hsa_circ_211786,RMVar_hsa_circ_211787 38111 RMVar_ID_38111 Human_SNP_ID_693367898 A-to-I Human chr21 + 32454058 32454058 32454058 CAAGACCAGCCTGGCCAATATGGTGAAACCCCATCTCTACTAATAATACAAAAATTAGCCGGGCA CAAGACCAGCCTGGCCAATATGGTGAAACCCCGTCTCTACTAATAATACAAAAATTAGCCGGGCA A G EVA1C Ensembl:ENSG00000166979 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1317619173 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_272160,RMVar_hsa_circ_319359,RMVar_hsa_circ_75137,RMVar_hsa_circ_271950,RMVar_hsa_circ_211786,RMVar_hsa_circ_211787 38112 RMVar_ID_38112 Human_SNP_ID_693367903 A-to-I Human chr21 + 32454090 32454090 32454090 ATCTCTACTAATAATACAAAAATTAGCCGGGCATGGTGGCACGCACCTGTAGTCCCAGCTACTTG ATCTCTACTAATAATACAAAAATTAGCCGGGCGTGGTGGCACGCACCTGTAGTCCCAGCTACTTG A G EVA1C Ensembl:ENSG00000166979 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1356989191 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_272160,RMVar_hsa_circ_319359,RMVar_hsa_circ_75137,RMVar_hsa_circ_271950,RMVar_hsa_circ_211786,RMVar_hsa_circ_211787 38113 RMVar_ID_38113 Human_SNP_ID_693368974 A-to-I Human chr21 + 32458611 32458611 32458611 TCAGGCAGTTCTCCTGCCTCAGCTTCCTGAGTAACTGGGACTACAGGCATGCACCACCACGCCTG TCAGGCAGTTCTCCTGCCTCAGCTTCCTGAGTCACTGGGACTACAGGCATGCACCACCACGCCTG A C EVA1C Ensembl:ENSG00000166979 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs9984127 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_272160,RMVar_hsa_circ_75137,RMVar_hsa_circ_271950,RMVar_hsa_circ_211787,RMVar_hsa_circ_211788,RMVar_hsa_circ_326372 38114 RMVar_ID_38114 Human_SNP_ID_693368975 A-to-I Human chr21 + 32458611 32458611 32458611 TCAGGCAGTTCTCCTGCCTCAGCTTCCTGAGTAACTGGGACTACAGGCATGCACCACCACGCCTG TCAGGCAGTTCTCCTGCCTCAGCTTCCTGAGTGACTGGGACTACAGGCATGCACCACCACGCCTG A G EVA1C Ensembl:ENSG00000166979 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs9984127 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_272160,RMVar_hsa_circ_75137,RMVar_hsa_circ_271950,RMVar_hsa_circ_211787,RMVar_hsa_circ_211788,RMVar_hsa_circ_326372 38115 RMVar_ID_38115 Human_SNP_ID_693378740 A-to-I Human chr21 + 32500419 32500419 32500419 GTGATCCACCTGCCTCAGCCTCCCAAAGTGCTAGAATTACAGGCATGAGCCATCATGCCCAGCCC GTGATCCACCTGCCTCAGCCTCCCAAAGTGCTGGAATTACAGGCATGAGCCATCATGCCCAGCCC A G EVA1C Ensembl:ENSG00000166979 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs762076680 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75137 38116 RMVar_ID_38116 Human_SNP_ID_693398029 A-to-I Human chr21 - 32582781 32582781 32582781 TGAGACCAGTCTGGGCAACATGGTGAACCCCCATCCCGAGTAAAAATACAAAAATTAGCGAAGTA TGAGACCAGTCTGGGCAACATGGTGAACCCCCCTCCCGAGTAAAAATACAAAAATTAGCGAAGTA T G CFAP298-TCP10L,TCP10L Ensembl:ENSG00000265590,Ensembl:ENSG00000242220 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1423240436 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_211791 38117 RMVar_ID_38117 Human_SNP_ID_693404418 A-to-I Human chr21 - 32607681 32607681 32607681 CAAATGAGAAGATGAAGCAAGTGTTAAAGAAGACTATAGAAGAAGCCAAAGCAATAATATCTAAG CAAATGAGAAGATGAAGCAAGTGTTAAAGAAGGCTATAGAAGAAGCCAAAGCAATAATATCTAAG T C CFAP298-TCP10L,CFAP298 Ensembl:ENSG00000265590,Ensembl:ENSG00000159079 Protein coding,Protein coding CDS,CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1330594485 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_64691,Human_RBP_ID_1607225,Human_RBP_ID_1935308,Human_RBP_ID_2701109,Human_RBP_ID_7038235,Human_RBP_ID_8235318,Human_RBP_ID_14248184,Human_RBP_ID_18534881,Human_RBP_ID_23009618,Human_RBP_ID_23115622,Human_RBP_ID_23923619,Human_RBP_ID_24546915,Human_RBP_ID_25637362,Human_RBP_ID_26344139,Human_RBP_ID_27820858 Human_Splice_Rec_2114812,Human_Splice_Rec_2114813,Human_Splice_Rec_2114834,Human_Splice_Rec_2114835,Human_Splice_Rec_2114856,Human_Splice_Rec_2114857,Human_Splice_Rec_2114886,Human_Splice_Rec_2114887,Human_Splice_Rec_2114908,Human_Splice_Rec_2114909,Human_Splice_Rec_2114938,Human_Splice_Rec_2114939,Human_Splice_Rec_2114956,Human_Splice_Rec_2114957,Human_Splice_Rec_2114976,Human_Splice_Rec_2114977,Human_Splice_Rec_2115012,Human_Splice_Rec_2115013,Human_Splice_Rec_2115026,Human_Splice_Rec_2115027,Human_Splice_Rec_2115044,Human_Splice_Rec_2115045,Human_Splice_Rec_2115074,Human_Splice_Rec_2115075,Human_Splice_Rec_2115098,Human_Splice_Rec_2115099,Human_Splice_Rec_2115112,Human_Splice_Rec_2115113,Human_Splice_Rec_2115122,Human_Splice_Rec_2115123,Human_Splice_Rec_2115134,Human_Splice_Rec_2115135,Human_Splice_Rec_2115145,Human_Splice_Rec_2115378,Human_Splice_Rec_2115379,Human_Splice_Rec_2115390,Human_Splice_Rec_2115391,Human_Splice_Rec_2115400,Human_Splice_Rec_2115401,Human_Splice_Rec_2115424,Human_Splice_Rec_2115425 RMVar_hsa_circ_417,RMVar_hsa_circ_356776,RMVar_hsa_circ_211793,RMVar_hsa_circ_62727,RMVar_hsa_circ_338740 38118 RMVar_ID_38118 Human_SNP_ID_693428468 A-to-I Human chr21 - 32710002 32710002 32710002 AGAGATGGGTTTTTTACCATGTTGGCCAGGCTAGTCTCAAACTCCTGACTTCAAGTGATCCTCCC AGAGATGGGTTTTTTACCATGTTGGCCAGGCTGGTCTCAAACTCCTGACTTCAAGTGATCCTCCC T C SYNJ1 Ensembl:ENSG00000159082 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1189027520 Functional Loss SNV dbSNP153 33..33 33 - - - 38119 RMVar_ID_38119 Human_SNP_ID_693431364 A-to-I Human chr21 - 32722333 32722332 32722334 GTTGGCCAGGCTGATCTGAACTCGTGAACTCAAGTGATCCACCTGCCTTGGCCTCCCAAAGTGCT GTTGGCCAGGCTGATCTGAACTCGTGAACTC__GTGATCCACCTGCCTTGGCCTCCCAAAGTGCT CTT C SYNJ1 Ensembl:ENSG00000159082 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs536519864 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_14249706 38120 RMVar_ID_38120 Human_SNP_ID_693438557 A-to-I Human chr21 - 32753202 32753202 32753202 CACCAGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGTGCCCAGCCGTATAAT CACCAGCCTCAGCCTCCCAAAGTGCTGGGATTGCAGGCGTGAGCCACCGTGCCCAGCCGTATAAT T C PAXBP1 Ensembl:ENSG00000159086 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1464121831 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_211812,RMVar_hsa_circ_14345,RMVar_hsa_circ_323636,RMVar_hsa_circ_325750,RMVar_hsa_circ_211803,RMVar_hsa_circ_211802,RMVar_hsa_circ_123315,RMVar_hsa_circ_107440,RMVar_hsa_circ_82267,RMVar_hsa_circ_211805,RMVar_hsa_circ_211806,RMVar_hsa_circ_329328,RMVar_hsa_circ_211804,RMVar_hsa_circ_297842,RMVar_hsa_circ_23682,RMVar_hsa_circ_61318,RMVar_hsa_circ_211810,RMVar_hsa_circ_16248,RMVar_hsa_circ_300719,RMVar_hsa_circ_21153,RMVar_hsa_circ_122537,RMVar_hsa_circ_354534,RMVar_hsa_circ_327981,RMVar_hsa_circ_293407,RMVar_hsa_circ_211813,RMVar_hsa_circ_126899,RMVar_hsa_circ_330208,RMVar_hsa_circ_211811,RMVar_hsa_circ_211815 38121 RMVar_ID_38121 Human_SNP_ID_693449601 A-to-I Human chr21 + 32797349 32797349 32797349 CAGCTCACTGCAAGCTCTGCCTCCCAGGTTCCAACGATTGTCTTGTCTCAGCCTCCTGAGTAGCT CAGCTCACTGCAAGCTCTGCCTCCCAGGTTCCCACGATTGTCTTGTCTCAGCCTCCTGAGTAGCT A C C21orf62-AS1 Ensembl:ENSG00000205930 lincRNA exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1165789867 Functional Loss SNV dbSNP153 33..33 33 - - - 38122 RMVar_ID_38122 Human_SNP_ID_693556900 A-to-I Human chr21 + 33242477 33242477 33242477 GTGTGTGTCCGGGCGCGGTGGCTCGCGCCTGTAATCCCTGCACTTTGGGAGGCCGAGGCAGGTGG GTGTGTGTCCGGGCGCGGTGGCTCGCGCCTGTCATCCCTGCACTTTGGGAGGCCGAGGCAGGTGG A C IFNAR2,AP000295.1 Ensembl:ENSG00000159110,Ensembl:ENSG00000249624 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1348518805 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_211818,RMVar_hsa_circ_295992,RMVar_hsa_circ_307730,RMVar_hsa_circ_318069,RMVar_hsa_circ_365046,RMVar_hsa_circ_302996,RMVar_hsa_circ_211822,RMVar_hsa_circ_211824,RMVar_hsa_circ_211825,RMVar_hsa_circ_211823,RMVar_hsa_circ_211820,RMVar_hsa_circ_211821,RMVar_hsa_circ_211819,RMVar_hsa_circ_211828,RMVar_hsa_circ_300159,RMVar_hsa_circ_319307,RMVar_hsa_circ_354276,RMVar_hsa_circ_303069,RMVar_hsa_circ_288656,RMVar_hsa_circ_211826,RMVar_hsa_circ_211827 38123 RMVar_ID_38123 Human_SNP_ID_693557203 A-to-I Human chr21 + 33243273 33243272 33243273 CCCAGCTAATTTTTTGTATTTTTAGTAGAGACAGGGTTTTGCCGTGTTGGCCAGGCTGATCTCGA CCCAGCTAATTTTTTGTATTTTTAGTAGAGAC_GGGTTTTGCCGTGTTGGCCAGGCTGATCTCGA CA C IFNAR2,AP000295.1 Ensembl:ENSG00000159110,Ensembl:ENSG00000249624 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1352553693 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_211818,RMVar_hsa_circ_295992,RMVar_hsa_circ_307730,RMVar_hsa_circ_318069,RMVar_hsa_circ_365046,RMVar_hsa_circ_302996,RMVar_hsa_circ_211822,RMVar_hsa_circ_211824,RMVar_hsa_circ_211825,RMVar_hsa_circ_211823,RMVar_hsa_circ_211820,RMVar_hsa_circ_211821,RMVar_hsa_circ_211819,RMVar_hsa_circ_211828,RMVar_hsa_circ_300159,RMVar_hsa_circ_319307,RMVar_hsa_circ_354276,RMVar_hsa_circ_303069,RMVar_hsa_circ_288656,RMVar_hsa_circ_211826,RMVar_hsa_circ_211827 38124 RMVar_ID_38124 Human_SNP_ID_693557217 A-to-I Human chr21 + 33243344 33243344 33243344 ACCTTGTGTGATCCACCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGACGTGAGCCACGACGC ACCTTGTGTGATCCACCCACCTCGGCCTCCCAGAGTGCTGGGATTACAGACGTGAGCCACGACGC A G IFNAR2,AP000295.1 Ensembl:ENSG00000159110,Ensembl:ENSG00000249624 Protein coding,Protein coding intron,intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs943936520 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_211818,RMVar_hsa_circ_295992,RMVar_hsa_circ_307730,RMVar_hsa_circ_318069,RMVar_hsa_circ_365046,RMVar_hsa_circ_302996,RMVar_hsa_circ_211822,RMVar_hsa_circ_211824,RMVar_hsa_circ_211825,RMVar_hsa_circ_211823,RMVar_hsa_circ_211820,RMVar_hsa_circ_211821,RMVar_hsa_circ_211819,RMVar_hsa_circ_211828,RMVar_hsa_circ_300159,RMVar_hsa_circ_319307,RMVar_hsa_circ_354276,RMVar_hsa_circ_303069,RMVar_hsa_circ_288656,RMVar_hsa_circ_211826,RMVar_hsa_circ_211827 38125 RMVar_ID_38125 Human_SNP_ID_693559459 A-to-I Human chr21 + 33251849 33251849 33251849 TTACGCCTGTAATCCCAGCACTTTGGAAGGCCAAGGCAGGCAGATCGCTTGCGGTCAGGAGTTCA TTACGCCTGTAATCCCAGCACTTTGGAAGGCCCAGGCAGGCAGATCGCTTGCGGTCAGGAGTTCA A C IFNAR2,AP000295.1 Ensembl:ENSG00000159110,Ensembl:ENSG00000249624 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1281874278 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_295992,RMVar_hsa_circ_318069,RMVar_hsa_circ_211822,RMVar_hsa_circ_211824,RMVar_hsa_circ_211825,RMVar_hsa_circ_211823,RMVar_hsa_circ_211821,RMVar_hsa_circ_64647,RMVar_hsa_circ_117901,RMVar_hsa_circ_300159,RMVar_hsa_circ_303069,RMVar_hsa_circ_211826,RMVar_hsa_circ_211827,RMVar_hsa_circ_63421,RMVar_hsa_circ_343463,RMVar_hsa_circ_211832 38126 RMVar_ID_38126 Human_SNP_ID_693561677 A-to-I Human chr21 + 33261237 33261237 33261237 TTTTGCATTTTTAGTAGAGATGGGGTTTTGCTATGTTGGCCAGGCTGGTCTTGAACTCCTGACTT TTTTGCATTTTTAGTAGAGATGGGGTTTTGCTCTGTTGGCCAGGCTGGTCTTGAACTCCTGACTT A C IFNAR2,AP000295.1 Ensembl:ENSG00000159110,Ensembl:ENSG00000249624 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1019183676 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_211824,RMVar_hsa_circ_211825,RMVar_hsa_circ_211823,RMVar_hsa_circ_117901,RMVar_hsa_circ_211832,RMVar_hsa_circ_211834,RMVar_hsa_circ_120412 38127 RMVar_ID_38127 Human_SNP_ID_693561678 A-to-I Human chr21 + 33261237 33261237 33261237 TTTTGCATTTTTAGTAGAGATGGGGTTTTGCTATGTTGGCCAGGCTGGTCTTGAACTCCTGACTT TTTTGCATTTTTAGTAGAGATGGGGTTTTGCTGTGTTGGCCAGGCTGGTCTTGAACTCCTGACTT A G IFNAR2,AP000295.1 Ensembl:ENSG00000159110,Ensembl:ENSG00000249624 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1019183676 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_211824,RMVar_hsa_circ_211825,RMVar_hsa_circ_211823,RMVar_hsa_circ_117901,RMVar_hsa_circ_211832,RMVar_hsa_circ_211834,RMVar_hsa_circ_120412 38128 RMVar_ID_38128 Human_SNP_ID_693562021 A-to-I Human chr21 + 33262565 33262565 33262565 TCATTAAGTTTATTTTTTATTTTTTTAGAGGCAAGGTCTCGCTAAGGGCTGGAATGCAGTGGCTA TCATTAAGTTTATTTTTTATTTTTTTAGAGGCGAGGTCTCGCTAAGGGCTGGAATGCAGTGGCTA A G IFNAR2,AP000295.1 Ensembl:ENSG00000159110,Ensembl:ENSG00000249624 Protein coding,Protein coding CDS,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs775882512 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2116392,Human_Splice_Rec_2116424,Human_Splice_Rec_2116502 RMVar_hsa_circ_211824,RMVar_hsa_circ_211825,RMVar_hsa_circ_211823,RMVar_hsa_circ_117901,RMVar_hsa_circ_211832,RMVar_hsa_circ_211834,RMVar_hsa_circ_120412 38129 RMVar_ID_38129 Human_SNP_ID_693562049 A-to-I Human chr21 + 33262623 33262623 33262623 GTGGCTATTCACAGGTGCAGTCATAATGCACTACAGTCTGAAACTCCTGAGCTCAAACAGTCGTC GTGGCTATTCACAGGTGCAGTCATAATGCACTGCAGTCTGAAACTCCTGAGCTCAAACAGTCGTC A G IFNAR2,AP000295.1 Ensembl:ENSG00000159110,Ensembl:ENSG00000249624 Protein coding,Protein coding CDS,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs9710 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_570892,Human_RBP_ID_14253037,Human_RBP_ID_17978741 Human_Splice_Rec_2116392,Human_Splice_Rec_2116424,Human_Splice_Rec_2116502 RMVar_hsa_circ_211824,RMVar_hsa_circ_211825,RMVar_hsa_circ_211823,RMVar_hsa_circ_117901,RMVar_hsa_circ_211832,RMVar_hsa_circ_211834,RMVar_hsa_circ_120412 38130 RMVar_ID_38130 Human_SNP_ID_693562600 A-to-I Human chr21 + 33264042 33264041 33264043 CACCATGCCTAGCAAATTTTTGTATTTTTAGTAGAGACAGGATTTTACCATGTTGGCCAGGCTGG CACCATGCCTAGCAAATTTTTGTATTTTTAGT__AGACAGGATTTTACCATGTTGGCCAGGCTGG TAG T IFNAR2,AP000295.1 Ensembl:ENSG00000159110,Ensembl:ENSG00000249624 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs946314449 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_211824,RMVar_hsa_circ_211825 38131 RMVar_ID_38131 Human_SNP_ID_693562601 A-to-I Human chr21 + 33264042 33264042 33264042 CACCATGCCTAGCAAATTTTTGTATTTTTAGTAGAGACAGGATTTTACCATGTTGGCCAGGCTGG CACCATGCCTAGCAAATTTTTGTATTTTTAGTGGAGACAGGATTTTACCATGTTGGCCAGGCTGG A G IFNAR2,AP000295.1 Ensembl:ENSG00000159110,Ensembl:ENSG00000249624 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1131673 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_211824,RMVar_hsa_circ_211825 38132 RMVar_ID_38132 Human_SNP_ID_693562604 A-to-I Human chr21 + 33264056 33264056 33264056 AATTTTTGTATTTTTAGTAGAGACAGGATTTTACCATGTTGGCCAGGCTGGTCTCAAACTCCTGA AATTTTTGTATTTTTAGTAGAGACAGGATTTTGCCATGTTGGCCAGGCTGGTCTCAAACTCCTGA A G IFNAR2,AP000295.1 Ensembl:ENSG00000159110,Ensembl:ENSG00000249624 Protein coding,Protein coding 3'UTR,intron GSE38233;GSE99789 cultured B-cells;esophageal squamous carcinoma cells,EC109 - 24183664,29796672 RNA-Seq:(High) rs11549017 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_211824,RMVar_hsa_circ_211825 38133 RMVar_ID_38133 Human_SNP_ID_693562835 A-to-I Human chr21 + 33264782 33264782 33264782 ATGCCTAAACAGGCGTATCGCTTGAGGCCAGTAATTCGAGACCAGCCTGGGCAACATGGCAAATC ATGCCTAAACAGGCGTATCGCTTGAGGCCAGTGATTCGAGACCAGCCTGGGCAACATGGCAAATC A G IFNAR2,AP000295.1 Ensembl:ENSG00000159110,Ensembl:ENSG00000249624 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1465898900 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25638246 RMVar_hsa_circ_211824,RMVar_hsa_circ_211825 38134 RMVar_ID_38134 Human_SNP_ID_693562870 A-to-I Human chr21 + 33264956 33264956 33264956 GAGGTTGCAGTGAGCCAAGATCATGTCACTGCACTTCAGCCTGGGTGACAGAACCAGACCCTGTC GAGGTTGCAGTGAGCCAAGATCATGTCACTGCCCTTCAGCCTGGGTGACAGAACCAGACCCTGTC A C IFNAR2,AP000295.1 Ensembl:ENSG00000159110,Ensembl:ENSG00000249624 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs3191758 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_211824,RMVar_hsa_circ_211825 38135 RMVar_ID_38135 Human_SNP_ID_693562871 A-to-I Human chr21 + 33264956 33264956 33264956 GAGGTTGCAGTGAGCCAAGATCATGTCACTGCACTTCAGCCTGGGTGACAGAACCAGACCCTGTC GAGGTTGCAGTGAGCCAAGATCATGTCACTGCGCTTCAGCCTGGGTGACAGAACCAGACCCTGTC A G IFNAR2,AP000295.1 Ensembl:ENSG00000159110,Ensembl:ENSG00000249624 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs3191758 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_211824,RMVar_hsa_circ_211825 38136 RMVar_ID_38136 Human_SNP_ID_693583920 A-to-I Human chr21 + 33341759 33341759 33341759 GCTGGAGTGCAATGGCACAATCACGGCTCACTACAGCCTCTGCCTCCTGGGTTCAAGTGACTCTC GCTGGAGTGCAATGGCACAATCACGGCTCACTGCAGCCTCTGCCTCCTGGGTTCAAGTGACTCTC A G IFNAR1 Ensembl:ENSG00000142166 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs755311551 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_211845,RMVar_hsa_circ_14454,RMVar_hsa_circ_299785,RMVar_hsa_circ_36852,RMVar_hsa_circ_275071,RMVar_hsa_circ_282508,RMVar_hsa_circ_211844,RMVar_hsa_circ_300188,RMVar_hsa_circ_281310,RMVar_hsa_circ_211847,RMVar_hsa_circ_211848,RMVar_hsa_circ_211846 38137 RMVar_ID_38137 Human_SNP_ID_693584576 A-to-I Human chr21 + 33344040 33344040 33344040 GGGCGTGGTGGCTCACGCCTGTAGTGGTAGCTACTTGGGAGGCTGAGGCACAAGAATCCCTTGAA GGGCGTGGTGGCTCACGCCTGTAGTGGTAGCTGCTTGGGAGGCTGAGGCACAAGAATCCCTTGAA A G IFNAR1 Ensembl:ENSG00000142166 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1457276322 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_299785,RMVar_hsa_circ_275071,RMVar_hsa_circ_282508,RMVar_hsa_circ_211844,RMVar_hsa_circ_300188,RMVar_hsa_circ_211847,RMVar_hsa_circ_211848,RMVar_hsa_circ_211846,RMVar_hsa_circ_56702,RMVar_hsa_circ_18588 38138 RMVar_ID_38138 Human_SNP_ID_693585702 A-to-I Human chr21 + 33348625 33348625 33348625 GGAGTTCAAGACCAGCCTGGCCAACATGACGAAACCCCATCTCTACTAAAAATACAAAAATTAGG GGAGTTCAAGACCAGCCTGGCCAACATGACGACACCCCATCTCTACTAAAAATACAAAAATTAGG A C IFNAR1 Ensembl:ENSG00000142166 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs960758364 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2116672,Human_Splice_Rec_2116682 RMVar_hsa_circ_275071,RMVar_hsa_circ_282508,RMVar_hsa_circ_211847,RMVar_hsa_circ_211848,RMVar_hsa_circ_211850,RMVar_hsa_circ_56702,RMVar_hsa_circ_18588,RMVar_hsa_circ_271152,RMVar_hsa_circ_332178,RMVar_hsa_circ_211849 38139 RMVar_ID_38139 Human_SNP_ID_693585707 A-to-I Human chr21 + 33348655 33348655 33348655 GAAACCCCATCTCTACTAAAAATACAAAAATTAGGCAGGCCTGGTGGCGTGCACCTGTAATCCCA GAAACCCCATCTCTACTAAAAATACAAAAATTTGGCAGGCCTGGTGGCGTGCACCTGTAATCCCA A T IFNAR1 Ensembl:ENSG00000142166 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1313196497 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_275071,RMVar_hsa_circ_282508,RMVar_hsa_circ_211847,RMVar_hsa_circ_211848,RMVar_hsa_circ_211850,RMVar_hsa_circ_56702,RMVar_hsa_circ_18588,RMVar_hsa_circ_271152,RMVar_hsa_circ_332178,RMVar_hsa_circ_211849 38140 RMVar_ID_38140 Human_SNP_ID_693587450 A-to-I Human chr21 + 33355829 33355829 33355829 CATGAGGTCAAGAGATCGAGACCAGCCTGGCCAACGTGGTGAAACCCCATCTCTACTAAAAATAC CATGAGGTCAAGAGATCGAGACCAGCCTGGCCGACGTGGTGAAACCCCATCTCTACTAAAAATAC A G IFNAR1 Ensembl:ENSG00000142166 Protein coding 3'UTR GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,29796672,31158229 RNA-Seq:(High) rs924660967 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_151209 38141 RMVar_ID_38141 Human_SNP_ID_693587501 A-to-I Human chr21 - 33356007 33356007 33356007 TGTCTCAACTCTTTTAATTTCTTTTTTTAAAGAGTCTCACGCTGTCACCAGGCTGGAGTGCAGTG TGTCTCAACTCTTTTAATTTCTTTTTTTAAAGCGTCTCACGCTGTCACCAGGCTGGAGTGCAGTG T G - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1312362052 Functional Loss SNV dbSNP153 33..33 33 - - - 38142 RMVar_ID_38142 Human_SNP_ID_693587926 A-to-I Human chr21 + 33357581 33357581 33357581 ACAGTCTCATTCTGTTGCCCAGGCTGGAGTGCAGTGGCTTGATCTCGGCTCACTGCAACCTCGCC ACAGTCTCATTCTGTTGCCCAGGCTGGAGTGCGGTGGCTTGATCTCGGCTCACTGCAACCTCGCC A G IFNAR1 Ensembl:ENSG00000142166 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs892694398 Functional Loss SNV dbSNP153 33..33 33 - - - 38143 RMVar_ID_38143 Human_SNP_ID_693587938 A-to-I Human chr21 + 33357600 33357600 33357600 CAGGCTGGAGTGCAGTGGCTTGATCTCGGCTCACTGCAACCTCGCCTCCCGGGTTCAAGCAATTC CAGGCTGGAGTGCAGTGGCTTGATCTCGGCTCGCTGCAACCTCGCCTCCCGGGTTCAAGCAATTC A G IFNAR1 Ensembl:ENSG00000142166 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1007183686 Functional Loss SNV dbSNP153 33..33 33 - - - 38144 RMVar_ID_38144 Human_SNP_ID_693587961 A-to-I Human chr21 + 33357665 33357665 33357665 TCTGCCGCAGCCTCCAGAGTAGCTGGGATAACAGGTGCCCACCACCACACCCCACTAATTTTTGT TCTGCCGCAGCCTCCAGAGTAGCTGGGATAACCGGTGCCCACCACCACACCCCACTAATTTTTGT A C IFNAR1 Ensembl:ENSG00000142166 Protein coding 3'UTR GSE47997;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,29129909,31158229,31158229 RNA-Seq:(High) rs1052268487 Functional Loss SNV dbSNP153 33..33 33 - - - 38145 RMVar_ID_38145 Human_SNP_ID_693587962 A-to-I Human chr21 + 33357665 33357665 33357665 TCTGCCGCAGCCTCCAGAGTAGCTGGGATAACAGGTGCCCACCACCACACCCCACTAATTTTTGT TCTGCCGCAGCCTCCAGAGTAGCTGGGATAACGGGTGCCCACCACCACACCCCACTAATTTTTGT A G IFNAR1 Ensembl:ENSG00000142166 Protein coding 3'UTR GSE47997;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,29129909,31158229,31158229 RNA-Seq:(High) rs1052268487 Functional Loss SNV dbSNP153 33..33 33 - - - 38146 RMVar_ID_38146 Human_SNP_ID_693587978 A-to-I Human chr21 + 33357739 33357739 33357739 TTTAGTAGAGATGGGGTTTCACCATGTTGGTCAGGCTGGTCTTGGACTCCTGACCTCATGCTCCA TTTAGTAGAGATGGGGTTTCACCATGTTGGTCGGGCTGGTCTTGGACTCCTGACCTCATGCTCCA A G IFNAR1 Ensembl:ENSG00000142166 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1242769197 Functional Loss SNV dbSNP153 33..33 33 - - - 38147 RMVar_ID_38147 Human_SNP_ID_693588517 A-to-I Human chr21 + 33360175 33360175 33360175 AAGAAAATGTTGGCAGTTCCAGCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAA AAGAAAATGTTGGCAGTTCCAGCCTGGCCAACGTGGTGAAACCCCGTCTCTACTAAAAATACAAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1172741689 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14254934 38148 RMVar_ID_38148 Human_SNP_ID_693599603 A-to-I Human chr21 + 33404555 33404555 33404555 CGCCTCCCGTGCTCAAGCGATCCTCCCACGTCAGCCTCCCAAGAAGGTGGTATTATTGGCCACGC CGCCTCCCGTGCTCAAGCGATCCTCCCACGTCGGCCTCCCAAGAAGGTGGTATTATTGGCCACGC A G IFNGR2 Ensembl:ENSG00000159128 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982362160 Functional Loss SNV dbSNP153 33..33 33 - - - 38149 RMVar_ID_38149 Human_SNP_ID_693599992 A-to-I Human chr21 + 33405855 33405855 33405855 GAGTTCAAGACCAGGCTGGTCAACAATGATGAAACCCCGTCTCTACCAAAAATACAAAAATTAGG GAGTTCAAGACCAGGCTGGTCAACAATGATGACACCCCGTCTCTACCAAAAATACAAAAATTAGG A C IFNGR2 Ensembl:ENSG00000159128 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031077976 Functional Loss SNV dbSNP153 33..33 33 - - - 38150 RMVar_ID_38150 Human_SNP_ID_693600234 A-to-I Human chr21 + 33406892 33406892 33406892 GCTGGTTTTGAACTCCTGGGGTCAAGAGATCCACCCGCCTCAGCCTCCCAAAGTGCTAGGATTAT GCTGGTTTTGAACTCCTGGGGTCAAGAGATCCCCCCGCCTCAGCCTCCCAAAGTGCTAGGATTAT A C IFNGR2 Ensembl:ENSG00000159128 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs996491394 Functional Loss SNV dbSNP153 33..33 33 - - - 38151 RMVar_ID_38151 Human_SNP_ID_693602451 A-to-I Human chr21 + 33415898 33415898 33415898 GTTGTTGTTGTTTTGAAACAGAGTTTCCCTCTATCGCCCAGGCTGGAGGGCAATGGCATGATCTC GTTGTTGTTGTTTTGAAACAGAGTTTCCCTCTGTCGCCCAGGCTGGAGGGCAATGGCATGATCTC A G IFNGR2 Ensembl:ENSG00000159128 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs111674001 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_323817,RMVar_hsa_circ_351098,RMVar_hsa_circ_211854,RMVar_hsa_circ_85090,RMVar_hsa_circ_280231,RMVar_hsa_circ_348674,RMVar_hsa_circ_289390,RMVar_hsa_circ_126558,RMVar_hsa_circ_211856,RMVar_hsa_circ_211857,RMVar_hsa_circ_211858,RMVar_hsa_circ_211855 38152 RMVar_ID_38152 Human_SNP_ID_693604357 A-to-I Human chr21 + 33423587 33423586 33423588 ACTATGCCCGTCTAATTTTTTGTATTTTTAGTAGAGACGGGATTTCACCATGTTGTCCAGGCTGG ACTATGCCCGTCTAATTTTTTGTATTTTTAGT__AGACGGGATTTCACCATGTTGTCCAGGCTGG TAG T IFNGR2 Ensembl:ENSG00000159128 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1163190947 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_351098,RMVar_hsa_circ_85090,RMVar_hsa_circ_348674,RMVar_hsa_circ_289390,RMVar_hsa_circ_126558,RMVar_hsa_circ_211856,RMVar_hsa_circ_211857,RMVar_hsa_circ_211858,RMVar_hsa_circ_211855,RMVar_hsa_circ_211860,RMVar_hsa_circ_280110,RMVar_hsa_circ_315285,RMVar_hsa_circ_211859 38153 RMVar_ID_38153 Human_SNP_ID_693604396 A-to-I Human chr21 + 33423737 33423737 33423737 ATAAAAAGTTTTTTAGAGAGGATCATGCCTGTAATCTTAGCCCATTGGGAGGCTGAGGTGGGAGG ATAAAAAGTTTTTTAGAGAGGATCATGCCTGTGATCTTAGCCCATTGGGAGGCTGAGGTGGGAGG A G IFNGR2 Ensembl:ENSG00000159128 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs574233826 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25638407 RMVar_hsa_circ_351098,RMVar_hsa_circ_85090,RMVar_hsa_circ_348674,RMVar_hsa_circ_289390,RMVar_hsa_circ_126558,RMVar_hsa_circ_211856,RMVar_hsa_circ_211857,RMVar_hsa_circ_211858,RMVar_hsa_circ_211855,RMVar_hsa_circ_211860,RMVar_hsa_circ_280110,RMVar_hsa_circ_315285,RMVar_hsa_circ_211859 38154 RMVar_ID_38154 Human_SNP_ID_693604493 A-to-I Human chr21 + 33424130 33424130 33424130 CAAGACCAGTCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAGTTAGCCGGGTA CAAGACCAGTCTGGCCAACATGGTGAAACCCCCTCTCTACTAAAAATACAAAAGTTAGCCGGGTA A C IFNGR2 Ensembl:ENSG00000159128 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1055729546 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_351098,RMVar_hsa_circ_85090,RMVar_hsa_circ_348674,RMVar_hsa_circ_289390,RMVar_hsa_circ_126558,RMVar_hsa_circ_211856,RMVar_hsa_circ_211857,RMVar_hsa_circ_211858,RMVar_hsa_circ_211855,RMVar_hsa_circ_211860,RMVar_hsa_circ_280110,RMVar_hsa_circ_315285,RMVar_hsa_circ_211859 38155 RMVar_ID_38155 Human_SNP_ID_693604662 A-to-I Human chr21 + 33424840 33424840 33424840 CTCAGTTCACTGCAGCCTCCGCCTCCAGGTTTAAGTGATTCTCGTGCCTCAGCCTCCCCAGTAGC CTCAGTTCACTGCAGCCTCCGCCTCCAGGTTTGAGTGATTCTCGTGCCTCAGCCTCCCCAGTAGC A G IFNGR2 Ensembl:ENSG00000159128 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs190468107 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_351098,RMVar_hsa_circ_85090,RMVar_hsa_circ_348674,RMVar_hsa_circ_289390,RMVar_hsa_circ_126558,RMVar_hsa_circ_211856,RMVar_hsa_circ_211857,RMVar_hsa_circ_211858,RMVar_hsa_circ_211855,RMVar_hsa_circ_211860,RMVar_hsa_circ_280110,RMVar_hsa_circ_315285,RMVar_hsa_circ_211859 38156 RMVar_ID_38156 Human_SNP_ID_693605712 A-to-I Human chr21 + 33428565 33428565 33428565 CATTTCATTATGGGGAATATGAAACTGGGAAGAGTGAGACTCACTGAAAAACAGACTTAGCATCT CATTTCATTATGGGGAATATGAAACTGGGAAGGGTGAGACTCACTGAAAAACAGACTTAGCATCT A G IFNGR2 Ensembl:ENSG00000159128 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs8130924 Functional Loss SNV dbSNP153,PGA 33..33 33 - - - GWAS_ID_4329,GWAS_ID_4330,GWAS_ID_4331,GWAS_ID_4332,GWAS_ID_4333 RMVar_hsa_circ_351098,RMVar_hsa_circ_85090,RMVar_hsa_circ_289390,RMVar_hsa_circ_126558,RMVar_hsa_circ_211856,RMVar_hsa_circ_211857,RMVar_hsa_circ_211858,RMVar_hsa_circ_280110,RMVar_hsa_circ_211859,RMVar_hsa_circ_115295,RMVar_hsa_circ_272764,RMVar_hsa_circ_211864,RMVar_hsa_circ_211865 38157 RMVar_ID_38157 Human_SNP_ID_693605896 A-to-I Human chr21 + 33429362 33429361 33429363 CACAGAGTCACACTCTGATTTCGTTTTGAGACAGAATTTCACTCTGTCTCCCAGGGTAGAGTGCA CACAGAGTCACACTCTGATTTCGTTTTGAGAC__AATTTCACTCTGTCTCCCAGGGTAGAGTGCA CAG C IFNGR2 Ensembl:ENSG00000159128 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1409130393 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_351098,RMVar_hsa_circ_85090,RMVar_hsa_circ_289390,RMVar_hsa_circ_126558,RMVar_hsa_circ_211856,RMVar_hsa_circ_211857,RMVar_hsa_circ_211858,RMVar_hsa_circ_280110,RMVar_hsa_circ_211859,RMVar_hsa_circ_115295,RMVar_hsa_circ_272764,RMVar_hsa_circ_211864,RMVar_hsa_circ_211865 38158 RMVar_ID_38158 Human_SNP_ID_693606371 A-to-I Human chr21 + 33431490 33431490 33431490 TACTCAGGAGTTGGAGGCAGGAGAATTGCTTGAACCTGGGAGGCGGAGGTTGCAGTGAGCCGAGG TACTCAGGAGTTGGAGGCAGGAGAATTGCTTGGACCTGGGAGGCGGAGGTTGCAGTGAGCCGAGG A G IFNGR2 Ensembl:ENSG00000159128 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1187009303 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_351098,RMVar_hsa_circ_85090,RMVar_hsa_circ_289390,RMVar_hsa_circ_126558,RMVar_hsa_circ_211856,RMVar_hsa_circ_211857,RMVar_hsa_circ_211858,RMVar_hsa_circ_280110,RMVar_hsa_circ_211859,RMVar_hsa_circ_115295,RMVar_hsa_circ_272764,RMVar_hsa_circ_211864,RMVar_hsa_circ_211865 38159 RMVar_ID_38159 Human_SNP_ID_693606457 A-to-I Human chr21 + 33431754 33431753 33431755 CACCACATCCAGCTAATTTTTGTACTTTTAGTAGAGACTGGGTTTTGCAATGTTGGCCAGGCTGG CACCACATCCAGCTAATTTTTGTACTTTTAGT__AGACTGGGTTTTGCAATGTTGGCCAGGCTGG TAG T IFNGR2 Ensembl:ENSG00000159128 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1191918590 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_351098,RMVar_hsa_circ_85090,RMVar_hsa_circ_289390,RMVar_hsa_circ_126558,RMVar_hsa_circ_211856,RMVar_hsa_circ_211857,RMVar_hsa_circ_211858,RMVar_hsa_circ_280110,RMVar_hsa_circ_211859,RMVar_hsa_circ_115295,RMVar_hsa_circ_272764,RMVar_hsa_circ_211864,RMVar_hsa_circ_211865 38160 RMVar_ID_38160 Human_SNP_ID_693606459 A-to-I Human chr21 + 33431770 33431770 33431770 TTTTTGTACTTTTAGTAGAGACTGGGTTTTGCAATGTTGGCCAGGCTGGTCTCTTAACTCCTGAC TTTTTGTACTTTTAGTAGAGACTGGGTTTTGCGATGTTGGCCAGGCTGGTCTCTTAACTCCTGAC A G IFNGR2 Ensembl:ENSG00000159128 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs948535347 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_351098,RMVar_hsa_circ_85090,RMVar_hsa_circ_289390,RMVar_hsa_circ_126558,RMVar_hsa_circ_211856,RMVar_hsa_circ_211857,RMVar_hsa_circ_211858,RMVar_hsa_circ_280110,RMVar_hsa_circ_211859,RMVar_hsa_circ_115295,RMVar_hsa_circ_272764,RMVar_hsa_circ_211864,RMVar_hsa_circ_211865 38161 RMVar_ID_38161 Human_SNP_ID_693606804 A-to-I Human chr21 + 33432909 33432908 33432910 TGTGCACACATCTCTTTTTTTTTTTTTGAGACAGGGTCTTGCTCTGTTGCCCAGGCGGGAGTGTC TGTGCACACATCTCTTTTTTTTTTTTTGAGAC__GGTCTTGCTCTGTTGCCCAGGCGGGAGTGTC CAG C IFNGR2 Ensembl:ENSG00000159128 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs764187616 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_22362177 RMVar_hsa_circ_114090,RMVar_hsa_circ_85090,RMVar_hsa_circ_211858,RMVar_hsa_circ_115295,RMVar_hsa_circ_211865,RMVar_hsa_circ_211867,RMVar_hsa_circ_125196,RMVar_hsa_circ_211871 38162 RMVar_ID_38162 Human_SNP_ID_693609782 A-to-I Human chr21 - 33444365 33444365 33444365 AATTGTATTTTTTGTAGAGACACGGTTTCACCATGTTGCCCAGATTGGTCTGGAGCTCCTGAGCT AATTGTATTTTTTGTAGAGACACGGTTTCACCGTGTTGCCCAGATTGGTCTGGAGCTCCTGAGCT T C TMEM50B Ensembl:ENSG00000142188 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027309977 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78125,RMVar_hsa_circ_123856,RMVar_hsa_circ_211868,RMVar_hsa_circ_211869,RMVar_hsa_circ_211873,RMVar_hsa_circ_75867,RMVar_hsa_circ_211874,RMVar_hsa_circ_211875 38163 RMVar_ID_38163 Human_SNP_ID_693614637 A-to-I Human chr21 - 33463240 33463240 33463240 TCACCCAGACTGGAGTACAGTGGTGCGATCTCAGCTCATTGCATCCTCCGCCTCCCAGGCTCAAG TCACCCAGACTGGAGTACAGTGGTGCGATCTCGGCTCATTGCATCCTCCGCCTCCCAGGCTCAAG T C TMEM50B Ensembl:ENSG00000142188 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1189249312 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78125,RMVar_hsa_circ_211869,RMVar_hsa_circ_73430,RMVar_hsa_circ_314355,RMVar_hsa_circ_211877,RMVar_hsa_circ_211876,RMVar_hsa_circ_301945,RMVar_hsa_circ_302587,RMVar_hsa_circ_265654 38164 RMVar_ID_38164 Human_SNP_ID_693625015 A-to-I Human chr21 - 33501416 33501416 33501416 GGTAGGAGGATTCCTTGAGCTCAGGAGGTCGAAGTTTCAGTGAGCTGTGATCGCACAACTGTACT GGTAGGAGGATTCCTTGAGCTCAGGAGGTCGAGGTTTCAGTGAGCTGTGATCGCACAACTGTACT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388984322 Functional Loss SNV dbSNP153 33..33 33 - - - 38165 RMVar_ID_38165 Human_SNP_ID_693628517 A-to-I Human chr21 - 33514208 33514208 33514208 ACTGGAGTTCCGTGGTGCGATCACAGCTCACTATTGCCCCAACGTCCTGGGTTCAAGTGATTCTC ACTGGAGTTCCGTGGTGCGATCACAGCTCACTGTTGCCCCAACGTCCTGGGTTCAAGTGATTCTC T C GART Ensembl:ENSG00000159131 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs570721942 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6781,RMVar_hsa_circ_38850,RMVar_hsa_circ_20820,RMVar_hsa_circ_41605,RMVar_hsa_circ_347799,RMVar_hsa_circ_24371 38166 RMVar_ID_38166 Human_SNP_ID_693631721 A-to-I Human chr21 - 33526211 33526211 33526211 AGCCGAGGTCGCACAACTGCACACTCCAGCCTAGGTGACAGAGCAAGACTCTGTCCCAAAAAGAA AGCCGAGGTCGCACAACTGCACACTCCAGCCTCGGTGACAGAGCAAGACTCTGTCCCAAAAAGAA T G GART Ensembl:ENSG00000159131 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-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 38167 RMVar_ID_38167 Human_SNP_ID_693632027 A-to-I Human chr21 - 33527435 33527435 33527435 TCTCGGCTCACTGTAACCTCCTCCTGGGTTCAAGCGATTCTTCTGACTCAGCCTCCCAAGTAACT TCTCGGCTCACTGTAACCTCCTCCTGGGTTCAGGCGATTCTTCTGACTCAGCCTCCCAAGTAACT T C GART Ensembl:ENSG00000159131 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1003766906 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2701507,Human_RBP_ID_14257618 RMVar_hsa_circ_41605,RMVar_hsa_circ_351341,RMVar_hsa_circ_54071,RMVar_hsa_circ_366176,RMVar_hsa_circ_46203 38168 RMVar_ID_38168 Human_SNP_ID_693632695 A-to-I Human chr21 - 33529581 33529581 33529581 GATGGCACATGCCTGTAGTCCCAGTCCCAGCTACTTGGGAAGCTAAGGTAAGAGAATCACTTGAA GATGGCACATGCCTGTAGTCCCAGTCCCAGCTGCTTGGGAAGCTAAGGTAAGAGAATCACTTGAA T C GART Ensembl:ENSG00000159131 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs925857163 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2117045 RMVar_hsa_circ_41605,RMVar_hsa_circ_351341,RMVar_hsa_circ_28455,RMVar_hsa_circ_54071,RMVar_hsa_circ_366176,RMVar_hsa_circ_46203,RMVar_hsa_circ_112077,RMVar_hsa_circ_34260,RMVar_hsa_circ_101387,RMVar_hsa_circ_211881,RMVar_hsa_circ_211882 38169 RMVar_ID_38169 Human_SNP_ID_693632841 A-to-I Human chr21 - 33530092 33530092 33530092 CACCTCCTGGGTTCAAGTGATTCTCCTGCCTCAGCCTCACAAGTAGCTGGGACTACAGGCACAGG CACCTCCTGGGTTCAAGTGATTCTCCTGCCTCTGCCTCACAAGTAGCTGGGACTACAGGCACAGG T A GART Ensembl:ENSG00000159131 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1335378658 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41605,RMVar_hsa_circ_351341,RMVar_hsa_circ_28455,RMVar_hsa_circ_54071,RMVar_hsa_circ_366176,RMVar_hsa_circ_46203,RMVar_hsa_circ_112077,RMVar_hsa_circ_34260,RMVar_hsa_circ_101387,RMVar_hsa_circ_211881,RMVar_hsa_circ_211882 38170 RMVar_ID_38170 Human_SNP_ID_693632848 A-to-I Human chr21 - 33530109 33530109 33530109 TGGCTCACTACATCCTCCACCTCCTGGGTTCAAGTGATTCTCCTGCCTCAGCCTCACAAGTAGCT TGGCTCACTACATCCTCCACCTCCTGGGTTCACGTGATTCTCCTGCCTCAGCCTCACAAGTAGCT T G GART Ensembl:ENSG00000159131 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1410815905 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41605,RMVar_hsa_circ_351341,RMVar_hsa_circ_28455,RMVar_hsa_circ_54071,RMVar_hsa_circ_366176,RMVar_hsa_circ_46203,RMVar_hsa_circ_112077,RMVar_hsa_circ_34260,RMVar_hsa_circ_101387,RMVar_hsa_circ_211881,RMVar_hsa_circ_211882 38171 RMVar_ID_38171 Human_SNP_ID_693637748 A-to-I Human chr21 + 33546698 33546698 33546698 AGCTACTTGGGAAGCTGAGGCAGGAGAATCGCATGAACCCAGGAGGCGAATGTTGCAGTGCGCTG AGCTACTTGGGAAGCTGAGGCAGGAGAATCGCGTGAACCCAGGAGGCGAATGTTGCAGTGCGCTG A G SON Ensembl:ENSG00000159140 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs961651241 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7040046,Human_RBP_ID_14258642 RMVar_hsa_circ_78630,RMVar_hsa_circ_121649,RMVar_hsa_circ_211887,RMVar_hsa_circ_211889 38172 RMVar_ID_38172 Human_SNP_ID_693637758 A-to-I Human chr21 - 33546734 33546734 33546734 TCTTGTCGCCCAGGCTGGAGTGCAATGGCGCAATCTCAGCGCACTGCAACATTCGCCTCCTGGGT TCTTGTCGCCCAGGCTGGAGTGCAATGGCGCAGTCTCAGCGCACTGCAACATTCGCCTCCTGGGT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910721303 Functional Loss SNV dbSNP153 33..33 33 - - - 38173 RMVar_ID_38173 Human_SNP_ID_693637912 A-to-I Human chr21 + 33547243 33547243 33547243 TGACCTCATGATCCGCACACCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGC TGACCTCATGATCCGCACACCTTGGCCTCCCAGAGTGCTGGGATTACAGGCGTGAGCCACCGCGC A G SON Ensembl:ENSG00000159140 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs909429943 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22723767 RMVar_hsa_circ_78630,RMVar_hsa_circ_121649,RMVar_hsa_circ_211887,RMVar_hsa_circ_211889 38174 RMVar_ID_38174 Human_SNP_ID_693639059 A-to-I Human chr21 + 33550462 33550462 33550462 CTCCAGTGCTGGAGTTACCTGGGCCCTCTGCTACCCCGGTGCCAGAGTTGCCAGGGCCCCTTTCT CTCCAGTGCTGGAGTTACCTGGGCCCTCTGCTGCCCCGGTGCCAGAGTTGCCAGGGCCCCTTTCT A G SON Ensembl:ENSG00000159140 Protein coding CDS GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1477796149 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1935765,Human_RBP_ID_8541250,Human_RBP_ID_8858712,Human_RBP_ID_9298840,Human_RBP_ID_17978906,Human_RBP_ID_18779857,Human_RBP_ID_22083118,Human_RBP_ID_22262305,Human_RBP_ID_22454116,Human_RBP_ID_22818397,Human_RBP_ID_26788809,Human_RBP_ID_27026662,Human_RBP_ID_27301170 Human_miRNA_ID_2784832 RMVar_hsa_circ_78630,RMVar_hsa_circ_121649,RMVar_hsa_circ_211887,RMVar_hsa_circ_89632,RMVar_hsa_circ_211889,RMVar_hsa_circ_211890 38175 RMVar_ID_38175 Human_SNP_ID_693639277 A-to-I Human chr21 + 33550950 33550950 33550950 CAGCCTTCGGTGACTGGGGTGCCAGAGTTGCCAGGGCTGCCTTCGGCAACTAGGGCACTGGAGTT CAGCCTTCGGTGACTGGGGTGCCAGAGTTGCCTGGGCTGCCTTCGGCAACTAGGGCACTGGAGTT A T SON Ensembl:ENSG00000159140 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_1027662,Human_RBP_ID_1603246,Human_RBP_ID_1935774,Human_RBP_ID_3661055,Human_RBP_ID_5472445,Human_RBP_ID_7040108,Human_RBP_ID_8541263,Human_RBP_ID_8858727,Human_RBP_ID_9298853,Human_RBP_ID_17701222,Human_RBP_ID_17978913,Human_RBP_ID_18463591,Human_RBP_ID_18779876,Human_RBP_ID_22082150,Human_RBP_ID_22262311,Human_RBP_ID_22453971,Human_RBP_ID_26762074,Human_RBP_ID_26788811,Human_RBP_ID_27489669 Human_miRNA_ID_2933179 RMVar_hsa_circ_78630,RMVar_hsa_circ_121649,RMVar_hsa_circ_211887,RMVar_hsa_circ_89632,RMVar_hsa_circ_211889,RMVar_hsa_circ_211890 38176 RMVar_ID_38176 Human_SNP_ID_693639307 A-to-I Human chr21 + 33551013 33551013 33551013 TTGTCGGGGCAGCCTGTGGCAACTGGGGCACTAGAGTTGCCTGGGCCGCTCATGGCAGCTGGGGC TTGTCGGGGCAGCCTGTGGCAACTGGGGCACTGGAGTTGCCTGGGCCGCTCATGGCAGCTGGGGC A G SON Ensembl:ENSG00000159140 Protein coding CDS GSE38233;GSE100210;GSE107867;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;ASD brains,temporal_cortex;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,30559470,32596459 RNA-Seq:(High) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_5240579,Human_RBP_ID_5503939,Human_RBP_ID_8541265,Human_RBP_ID_8858727,Human_RBP_ID_9299247,Human_RBP_ID_9354192,Human_RBP_ID_14258941,Human_RBP_ID_18463767,Human_RBP_ID_22083138,Human_RBP_ID_23007238,Human_RBP_ID_26788896 RMVar_hsa_circ_78630,RMVar_hsa_circ_121649,RMVar_hsa_circ_211887,RMVar_hsa_circ_89632,RMVar_hsa_circ_211889,RMVar_hsa_circ_211890 38177 RMVar_ID_38177 Human_SNP_ID_693639579 A-to-I Human chr21 - 33551628 33551628 33551628 GAGCTGGTTGCTAACATCTGGGAGTCCATGGAACTGGTTGCTAACATCTGGGAGTCCATAGTGCT GAGCTGGTTGCTAACATCTGGGAGTCCATGGAGCTGGTTGCTAACATCTGGGAGTCCATAGTGCT T C - - Other Unknown GSE56152 embryonic stem cells,wild type - 25708366 RNA-Seq:(High) rs200724919 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - GWAS_ID_4334 38178 RMVar_ID_38178 Human_SNP_ID_693639654 A-to-I Human chr21 + 33551799 33551799 33551799 TTAGCAACCAGCACCATGGACTCCCAGATGTTAGCAACTAGCTCAATGGATTCCCAGATGTTAGC TTAGCAACCAGCACCATGGACTCCCAGATGTTGGCAACTAGCTCAATGGATTCCCAGATGTTAGC A G SON Ensembl:ENSG00000159140 Protein coding CDS GSE56152;GSE100210 embryonic stem cells,wild type;HepG2 cell line - 25708366,29129909 RNA-Seq:(High) rs17340257 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_245136,Human_RBP_ID_780250,Human_RBP_ID_1603278,Human_RBP_ID_1935785,Human_RBP_ID_7040132,Human_RBP_ID_8858751,Human_RBP_ID_14258998,Human_RBP_ID_17397363,Human_RBP_ID_18779903,Human_RBP_ID_22262323,Human_RBP_ID_23007256,Human_RBP_ID_27301184 RMVar_hsa_circ_78630,RMVar_hsa_circ_121649,RMVar_hsa_circ_211887,RMVar_hsa_circ_89632,RMVar_hsa_circ_211889,RMVar_hsa_circ_211890 38179 RMVar_ID_38179 Human_SNP_ID_693639675 A-to-I Human chr21 - 33551835 33551835 33551835 CCAGAAGCTAACATTTGAGAGTCCATAGTGCCAGATGCTAACATCTGGGAATCCATTGAGCTAGT CCAGAAGCTAACATTTGAGAGTCCATAGTGCCGGATGCTAACATCTGGGAATCCATTGAGCTAGT T C - - Other Unknown GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) - Functional Loss SNV HGVD 33..33 33 - - - 38180 RMVar_ID_38180 Human_SNP_ID_693641738 A-to-I Human chr21 + 33557387 33557387 33557387 TATTCCAGTGATGTTGACTCTGGAGCGTGCCAAAACCCGAATTGTGGGCAGAACTGATAATGGCT TATTCCAGTGATGTTGACTCTGGAGCGTGCCAGAACCCGAATTGTGGGCAGAACTGATAATGGCT A G SON Ensembl:ENSG00000159140 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs890521208 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1603410,Human_RBP_ID_17619947 RMVar_hsa_circ_78630,RMVar_hsa_circ_121649,RMVar_hsa_circ_211887,RMVar_hsa_circ_89632,RMVar_hsa_circ_211889,RMVar_hsa_circ_211890,RMVar_hsa_circ_211893,RMVar_hsa_circ_83885,RMVar_hsa_circ_85750,RMVar_hsa_circ_211894 38181 RMVar_ID_38181 Human_SNP_ID_693651300 A-to-I Human chr21 - 33591846 33591845 33591846 TCAAGGGATCCTCCTGCCTCAGCCTCCCCAGTAGCTGGGGCAACAGGCACATGCCACCATGCCTG TCAAGGGATCCTCCTGCCTCAGCCTCCCCAGT_GCTGGGGCAACAGGCACATGCCACCATGCCTG CT C CRYZL1,AP000311.1 Ensembl:ENSG00000205758,Ensembl:ENSG00000249209 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1431738287 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_121712,RMVar_hsa_circ_211911,RMVar_hsa_circ_96410,RMVar_hsa_circ_211910 38182 RMVar_ID_38182 Human_SNP_ID_693651307 A-to-I Human chr21 - 33591875 33591875 33591875 CAGCTCACTGTAACCTCAAACCCATGTGCTCAAGGGATCCTCCTGCCTCAGCCTCCCCAGTAGCT CAGCTCACTGTAACCTCAAACCCATGTGCTCAGGGGATCCTCCTGCCTCAGCCTCCCCAGTAGCT T C CRYZL1,AP000311.1 Ensembl:ENSG00000205758,Ensembl:ENSG00000249209 Protein coding,Protein coding intron,intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs917217264 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121712,RMVar_hsa_circ_211911,RMVar_hsa_circ_96410,RMVar_hsa_circ_211910 38183 RMVar_ID_38183 Human_SNP_ID_693651324 A-to-I Human chr21 - 33591945 33591945 33591945 TCTTTCTTTTTTTTTTTCTTTTGAGACAGGGTATTGCTCTGTTGCCCTGGCTGGAGTGCAGTGCT TCTTTCTTTTTTTTTTTCTTTTGAGACAGGGTGTTGCTCTGTTGCCCTGGCTGGAGTGCAGTGCT T C CRYZL1,AP000311.1 Ensembl:ENSG00000205758,Ensembl:ENSG00000249209 Protein coding,Protein coding intron,intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1451911791 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17572451 RMVar_hsa_circ_121712,RMVar_hsa_circ_211911,RMVar_hsa_circ_96410,RMVar_hsa_circ_211910 38184 RMVar_ID_38184 Human_SNP_ID_693651459 A-to-I Human chr21 - 33592336 33592336 33592336 TCTCAGGAGTTTGAGACCAGCCCGGGCAACATAGGGAGACCCTGTCTATACAAAAATAAAAATAA TCTCAGGAGTTTGAGACCAGCCCGGGCAACATCGGGAGACCCTGTCTATACAAAAATAAAAATAA T G CRYZL1,AP000311.1 Ensembl:ENSG00000205758,Ensembl:ENSG00000249209 Protein coding,Protein coding intron,intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs961656015 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121712,RMVar_hsa_circ_211911,RMVar_hsa_circ_96410,RMVar_hsa_circ_211910 38185 RMVar_ID_38185 Human_SNP_ID_693651553 A-to-I Human chr21 - 33592795 33592795 33592795 CACCTGCTACAGCCTCCCAAAATGCTGGGATTACAGGCGTTAGCCACCGCACCCAGCCCTAATTT CACCTGCTACAGCCTCCCAAAATGCTGGGATTGCAGGCGTTAGCCACCGCACCCAGCCCTAATTT T C CRYZL1,AP000311.1 Ensembl:ENSG00000205758,Ensembl:ENSG00000249209 Protein coding,Protein coding intron,intron GSE38233;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;ASD brains,cerebellum;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,30559470,31158229,31158229 RNA-Seq:(High) rs909622319 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121712,RMVar_hsa_circ_211911,RMVar_hsa_circ_96410,RMVar_hsa_circ_211910 38186 RMVar_ID_38186 Human_SNP_ID_693651570 A-to-I Human chr21 - 33592869 33592869 33592869 TTTTGTATTTTTAGTAGAGGCAGGATTTCACCATATTGGTCAGGCTGGTCTCGAACTCTTGACCT TTTTGTATTTTTAGTAGAGGCAGGATTTCACCGTATTGGTCAGGCTGGTCTCGAACTCTTGACCT T C CRYZL1,AP000311.1 Ensembl:ENSG00000205758,Ensembl:ENSG00000249209 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1033131898 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121712,RMVar_hsa_circ_211911,RMVar_hsa_circ_96410,RMVar_hsa_circ_211910 38187 RMVar_ID_38187 Human_SNP_ID_693651591 A-to-I Human chr21 - 33592952 33592952 33592952 TGCCTCCCAGGTTCAAGCAATTCTCCTGTCTCAGCCTCCCAAGTAGCTGAGACTATAGGCGCATG TGCCTCCCAGGTTCAAGCAATTCTCCTGTCTCGGCCTCCCAAGTAGCTGAGACTATAGGCGCATG T C CRYZL1,AP000311.1 Ensembl:ENSG00000205758,Ensembl:ENSG00000249209 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1182569369 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121712,RMVar_hsa_circ_211911,RMVar_hsa_circ_96410,RMVar_hsa_circ_211910 38188 RMVar_ID_38188 Human_SNP_ID_693651803 A-to-I Human chr21 - 33593720 33593720 33593720 CCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGGGCCACCACTCCCGGCTGTAGCTATTAGTT CCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGGGCCACCACTCCCGGCTGTAGCTATTAGTT T C CRYZL1,AP000311.1 Ensembl:ENSG00000205758,Ensembl:ENSG00000249209 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1479076310 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121712,RMVar_hsa_circ_211911,RMVar_hsa_circ_96410,RMVar_hsa_circ_211910 38189 RMVar_ID_38189 Human_SNP_ID_693651819 A-to-I Human chr21 - 33593800 33593800 33593800 TTTGTATTTTTTAGTAGAGACGGAGTTTCACCATGTTGGTCAAGCTGGTCTCAAACGCCTAACCT TTTGTATTTTTTAGTAGAGACGGAGTTTCACCGTGTTGGTCAAGCTGGTCTCAAACGCCTAACCT T C CRYZL1,AP000311.1 Ensembl:ENSG00000205758,Ensembl:ENSG00000249209 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs137949851 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121712,RMVar_hsa_circ_211911,RMVar_hsa_circ_96410,RMVar_hsa_circ_211910 38190 RMVar_ID_38190 Human_SNP_ID_693651820 A-to-I Human chr21 - 33593800 33593800 33593800 TTTGTATTTTTTAGTAGAGACGGAGTTTCACCATGTTGGTCAAGCTGGTCTCAAACGCCTAACCT TTTGTATTTTTTAGTAGAGACGGAGTTTCACCCTGTTGGTCAAGCTGGTCTCAAACGCCTAACCT T G CRYZL1,AP000311.1 Ensembl:ENSG00000205758,Ensembl:ENSG00000249209 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs137949851 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121712,RMVar_hsa_circ_211911,RMVar_hsa_circ_96410,RMVar_hsa_circ_211910 38191 RMVar_ID_38191 Human_SNP_ID_693651840 A-to-I Human chr21 - 33593857 33593857 33593857 TCTCAGCCTCCTGAGTAGCTGGGATTACAGACATGCGCCACCACGCCTGGCTAATTTTTTGTATT TCTCAGCCTCCTGAGTAGCTGGGATTACAGACGTGCGCCACCACGCCTGGCTAATTTTTTGTATT T C CRYZL1,AP000311.1 Ensembl:ENSG00000205758,Ensembl:ENSG00000249209 Protein coding,Protein coding intron,intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1212625370 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121712,RMVar_hsa_circ_211911,RMVar_hsa_circ_96410,RMVar_hsa_circ_211910 38192 RMVar_ID_38192 Human_SNP_ID_693651852 A-to-I Human chr21 - 33593885 33593885 33593885 CAACTCCTGGGTTCAAGCAATTCTCCTGTCTCAGCCTCCTGAGTAGCTGGGATTACAGACATGCG CAACTCCTGGGTTCAAGCAATTCTCCTGTCTCGGCCTCCTGAGTAGCTGGGATTACAGACATGCG T C CRYZL1,AP000311.1 Ensembl:ENSG00000205758,Ensembl:ENSG00000249209 Protein coding,Protein coding intron,intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1448414711 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121712,RMVar_hsa_circ_211911,RMVar_hsa_circ_96410,RMVar_hsa_circ_211910 38193 RMVar_ID_38193 Human_SNP_ID_693651857 A-to-I Human chr21 - 33593903 33593903 33593903 TTGGCTCACTGCAACCTCCAACTCCTGGGTTCAAGCAATTCTCCTGTCTCAGCCTCCTGAGTAGC TTGGCTCACTGCAACCTCCAACTCCTGGGTTCGAGCAATTCTCCTGTCTCAGCCTCCTGAGTAGC T C CRYZL1,AP000311.1 Ensembl:ENSG00000205758,Ensembl:ENSG00000249209 Protein coding,Protein coding intron,intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1390883832 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121712,RMVar_hsa_circ_211911,RMVar_hsa_circ_96410,RMVar_hsa_circ_211910 38194 RMVar_ID_38194 Human_SNP_ID_693651951 A-to-I Human chr21 - 33594230 33594230 33594230 GGAATTGCTTGAACCCAGGCAGTGAAGGTTGCAGTGAGCTGAGATCGCGCCACTGCACTCCAGCT GGAATTGCTTGAACCCAGGCAGTGAAGGTTGCCGTGAGCTGAGATCGCGCCACTGCACTCCAGCT T G CRYZL1,AP000311.1 Ensembl:ENSG00000205758,Ensembl:ENSG00000249209 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1484203696 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121712,RMVar_hsa_circ_211911,RMVar_hsa_circ_96410,RMVar_hsa_circ_211910 38195 RMVar_ID_38195 Human_SNP_ID_693651986 A-to-I Human chr21 - 33594366 33594365 33594366 ACGAGGTCAGGAAATCGAGACCATCCTGGCTAACATGATGAAACCCCGTCTCTATTAAAAATACC ACGAGGTCAGGAAATCGAGACCATCCTGGCTA_CATGATGAAACCCCGTCTCTATTAAAAATACC GT G CRYZL1,AP000311.1 Ensembl:ENSG00000205758,Ensembl:ENSG00000249209 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs556322762 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_121712,RMVar_hsa_circ_211911,RMVar_hsa_circ_96410,RMVar_hsa_circ_211910 38196 RMVar_ID_38196 Human_SNP_ID_693651990 A-to-I Human chr21 - 33594390 33594390 33594390 TTTGGGAGGCCGAGGTGGGGGATCACGAGGTCAGGAAATCGAGACCATCCTGGCTAACATGATGA TTTGGGAGGCCGAGGTGGGGGATCACGAGGTCGGGAAATCGAGACCATCCTGGCTAACATGATGA T C CRYZL1,AP000311.1 Ensembl:ENSG00000205758,Ensembl:ENSG00000249209 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1321988516 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121712,RMVar_hsa_circ_211911,RMVar_hsa_circ_96410,RMVar_hsa_circ_211910 38197 RMVar_ID_38197 Human_SNP_ID_693652079 A-to-I Human chr21 - 33594710 33594710 33594710 TGAACCTGGGAGGCAGAGGTTTCAGTGAGCCAAGATTGCACTACTACACTCCAGCCTGGTGACAG TGAACCTGGGAGGCAGAGGTTTCAGTGAGCCACGATTGCACTACTACACTCCAGCCTGGTGACAG T G CRYZL1,AP000311.1 Ensembl:ENSG00000205758,Ensembl:ENSG00000249209 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1402964932 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121712,RMVar_hsa_circ_211911,RMVar_hsa_circ_96410,RMVar_hsa_circ_211910 38198 RMVar_ID_38198 Human_SNP_ID_693652665 A-to-I Human chr21 - 33597043 33597043 33597043 CAACATGGTGAAACCCCATCTCTACAAAAAATACAAAAATTAGCCAGGCATGGTGGCACAGGCTT CAACATGGTGAAACCCCATCTCTACAAAAAATTCAAAAATTAGCCAGGCATGGTGGCACAGGCTT T A CRYZL1,AP000311.1 Ensembl:ENSG00000205758,Ensembl:ENSG00000249209 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs945231599 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8330,RMVar_hsa_circ_121712,RMVar_hsa_circ_211911,RMVar_hsa_circ_349022 38199 RMVar_ID_38199 Human_SNP_ID_693652692 A-to-I Human chr21 - 33597145 33597145 33597145 AAAATCTGGGCCAGGCATGGTGGCTCACACCTATGAGTCCAGCACTATGGGAGGCCGCGGCGGGC AAAATCTGGGCCAGGCATGGTGGCTCACACCTGTGAGTCCAGCACTATGGGAGGCCGCGGCGGGC T C CRYZL1,AP000311.1 Ensembl:ENSG00000205758,Ensembl:ENSG00000249209 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1200086008 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8330,RMVar_hsa_circ_121712,RMVar_hsa_circ_211911,RMVar_hsa_circ_349022 38200 RMVar_ID_38200 Human_SNP_ID_693679012 A-to-I Human chr21 + 33701011 33701011 33701011 GTGTGTGTGTGTTTTCTTATAGATGTGGTCTCACTCTGTTTCCCAGGCTGAAGTGCAGTGGTGCA GTGTGTGTGTGTTTTCTTATAGATGTGGTCTCCCTCTGTTTCCCAGGCTGAAGTGCAGTGGTGCA A C ITSN1 Ensembl:ENSG00000205726 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1368700369 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23924671 RMVar_hsa_circ_311861,RMVar_hsa_circ_338052 38201 RMVar_ID_38201 Human_SNP_ID_693679013 A-to-I Human chr21 + 33701011 33701011 33701011 GTGTGTGTGTGTTTTCTTATAGATGTGGTCTCACTCTGTTTCCCAGGCTGAAGTGCAGTGGTGCA GTGTGTGTGTGTTTTCTTATAGATGTGGTCTCTCTCTGTTTCCCAGGCTGAAGTGCAGTGGTGCA A T ITSN1 Ensembl:ENSG00000205726 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1368700369 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23924671 RMVar_hsa_circ_311861,RMVar_hsa_circ_338052 38202 RMVar_ID_38202 Human_SNP_ID_693691178 A-to-I Human chr21 + 33749088 33749088 33749088 GTGGCTCACTGTAGCCTCAACCTCTTCGGCATAAGTGATCCTCCCACCTCAGCCTTCCATGTAGC GTGGCTCACTGTAGCCTCAACCTCTTCGGCATGAGTGATCCTCCCACCTCAGCCTTCCATGTAGC A G ITSN1 Ensembl:ENSG00000205726 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049606863 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_53649,RMVar_hsa_circ_338624,RMVar_hsa_circ_367983,RMVar_hsa_circ_373378,RMVar_hsa_circ_367680,RMVar_hsa_circ_42984,RMVar_hsa_circ_211922,RMVar_hsa_circ_32906,RMVar_hsa_circ_42436,RMVar_hsa_circ_71588,RMVar_hsa_circ_366225,RMVar_hsa_circ_348994,RMVar_hsa_circ_368089,RMVar_hsa_circ_330403,RMVar_hsa_circ_211924 38203 RMVar_ID_38203 Human_SNP_ID_693702612 A-to-I Human chr21 + 33796144 33796144 33796144 TGCTACCACGCCCAGCTAATTTTTATATTATTAGTAGAGATGGGGTTTCACCATGTTGGTCTAGA TGCTACCACGCCCAGCTAATTTTTATATTATTGGTAGAGATGGGGTTTCACCATGTTGGTCTAGA A G ITSN1 Ensembl:ENSG00000205726 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334057502 Functional Loss SNV dbSNP153 33..33 33 - - - 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_211936 38204 RMVar_ID_38204 Human_SNP_ID_693729522 A-to-I Human chr21 - 33904819 33904819 33904819 GGAGAATCACTTGAACCTGGGAGGCGGAGGCTACAGTAAGCCGAGATCTCGCCACTCTACTCCAG GGAGAATCACTTGAACCTGGGAGGCGGAGGCTGCAGTAAGCCGAGATCTCGCCACTCTACTCCAG T C AP000311.1,ATP5PO Ensembl:ENSG00000249209,Ensembl:ENSG00000241837 Protein coding,Protein coding intron,intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1411467842 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98009,RMVar_hsa_circ_115868,RMVar_hsa_circ_211954,RMVar_hsa_circ_79245,RMVar_hsa_circ_211955,RMVar_hsa_circ_73129,RMVar_hsa_circ_211953,RMVar_hsa_circ_70601 38205 RMVar_ID_38205 Human_SNP_ID_693729537 A-to-I Human chr21 - 33904861 33904861 33904861 TGGCATGCGCCTGTAATTCCAGCTACTTGGGAAGCTGAGGCAGGAGAATCACTTGAACCTGGGAG TGGCATGCGCCTGTAATTCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCACTTGAACCTGGGAG T C AP000311.1,ATP5PO Ensembl:ENSG00000249209,Ensembl:ENSG00000241837 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1265825521 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98009,RMVar_hsa_circ_115868,RMVar_hsa_circ_211954,RMVar_hsa_circ_79245,RMVar_hsa_circ_211955,RMVar_hsa_circ_73129,RMVar_hsa_circ_211953,RMVar_hsa_circ_70601 38206 RMVar_ID_38206 Human_SNP_ID_693729554 A-to-I Human chr21 - 33904909 33904909 33904909 TGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCCGGGTGTGATGGCATGCGCCTGTAAT TGGTGAAACCCCGTCTCTACTAAAAATACAAACATTAGCCGGGTGTGATGGCATGCGCCTGTAAT T G AP000311.1,ATP5PO Ensembl:ENSG00000249209,Ensembl:ENSG00000241837 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1249784627 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98009,RMVar_hsa_circ_115868,RMVar_hsa_circ_211954,RMVar_hsa_circ_79245,RMVar_hsa_circ_211955,RMVar_hsa_circ_73129,RMVar_hsa_circ_211953,RMVar_hsa_circ_70601 38207 RMVar_ID_38207 Human_SNP_ID_693730280 A-to-I Human chr21 - 33907740 33907740 33907740 CACACTGCAGCCTTAAACTCCTAGGCTCAAGCAATCTTCCTGCCTCAGCCTCCTGAGTAGCTGGG CACACTGCAGCCTTAAACTCCTAGGCTCAAGCTATCTTCCTGCCTCAGCCTCCTGAGTAGCTGGG T A AP000311.1,ATP5PO Ensembl:ENSG00000249209,Ensembl:ENSG00000241837 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1465607123 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3523,RMVar_hsa_circ_98009,RMVar_hsa_circ_115868,RMVar_hsa_circ_211954,RMVar_hsa_circ_79245,RMVar_hsa_circ_211955,RMVar_hsa_circ_73129,RMVar_hsa_circ_211953,RMVar_hsa_circ_70601,RMVar_hsa_circ_281525,RMVar_hsa_circ_211959 38208 RMVar_ID_38208 Human_SNP_ID_693746139 A-to-I Human chr21 + 33972861 33972860 33972862 ATGATGGGATGTGCCTGTGGTTCCAGCTACTCAGGAGGCAGGTGGGAGGATGGCTTGAGTCAGAA ATGATGGGATGTGCCTGTGGTTCCAGCTACTC__GAGGCAGGTGGGAGGATGGCTTGAGTCAGAA CAG C LINC00649 Ensembl:ENSG00000237945 lincRNA exon GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1272471004 Functional Loss DEL dbSNP153 33..34 33 - - - 38209 RMVar_ID_38209 Human_SNP_ID_693779123 A-to-I Human chr21 + 34104731 34104731 34104731 GATGAGGGGAAGAAGATTACCAGAAGTGCAGGAAAGAGAAGTTTGAGGAACACCCTTGGCTTAGC GATGAGGGGAAGAAGATTACCAGAAGTGCAGGGAAGAGAAGTTTGAGGAACACCCTTGGCTTAGC A G SLC5A3,AP000317.2,MRPS6 Ensembl:ENSG00000198743,Ensembl:ENSG00000272657,Ensembl:ENSG00000243927 Protein coding,lincRNA,Protein coding 3'UTR,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs369369737 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_780084,Human_RBP_ID_832466,Human_RBP_ID_1100881,Human_RBP_ID_1607336,Human_RBP_ID_3667420,Human_RBP_ID_5089434,Human_RBP_ID_5653275,Human_RBP_ID_10035095,Human_RBP_ID_14269459,Human_RBP_ID_17981511,Human_RBP_ID_18325973,Human_RBP_ID_22395876 Human_miRNA_ID_2517799,Human_miRNA_ID_2517800,Human_miRNA_ID_3000010,Human_miRNA_ID_3000011,Human_miRNA_ID_3119225,Human_miRNA_ID_3119226 RMVar_hsa_circ_211963,RMVar_hsa_circ_76305,RMVar_hsa_circ_290271 38210 RMVar_ID_38210 Human_SNP_ID_693780532 A-to-I Human chr21 + 34110244 34110244 34110244 CAGCACTTTTGGGAGGCTGAGGCTGGTGGATCACTTGAGCCCAGGAGTTCGAGACCAGCTTGGGC CAGCACTTTTGGGAGGCTGAGGCTGGTGGATCGCTTGAGCCCAGGAGTTCGAGACCAGCTTGGGC A G AP000317.2,MRPS6 Ensembl:ENSG00000272657,Ensembl:ENSG00000243927 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1448921815 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_290271 38211 RMVar_ID_38211 Human_SNP_ID_693840507 A-to-I Human chr21 + 34366923 34366923 34366923 ATGGCGTAAACCCGGGAGGCAGAGCTTGCAGTAAGCCGAGATCGCGCCACTGCACTCCAGCCTGG ATGGCGTAAACCCGGGAGGCAGAGCTTGCAGTGAGCCGAGATCGCGCCACTGCACTCCAGCCTGG A G KCNE2 Ensembl:ENSG00000159197 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs149134319 Functional Loss SNV dbSNP153 33..33 33 - - - 38212 RMVar_ID_38212 Human_SNP_ID_693843194 A-to-I Human chr21 + 34378824 34378823 34378824 GTAATATCCTCTGAACCAAAGTGCTGTCATTTAAAAAATCAGAATCTAAAGAACAATTCTGCAAC GTAATATCCTCTGAACCAAAGTGCTGTCATTT_AAAAATCAGAATCTAAAGAACAATTCTGCAAC TA T SMIM11A Ensembl:ENSG00000205670 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1568816613 Functional Loss DEL dbSNP153 33..33 33 - - - 38213 RMVar_ID_38213 Human_SNP_ID_693843195 A-to-I Human chr21 + 34378824 34378824 34378824 GTAATATCCTCTGAACCAAAGTGCTGTCATTTAAAAAATCAGAATCTAAAGAACAATTCTGCAAC GTAATATCCTCTGAACCAAAGTGCTGTCATTTGAAAAATCAGAATCTAAAGAACAATTCTGCAAC A G SMIM11A Ensembl:ENSG00000205670 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1458547980 Functional Loss SNV dbSNP153 33..33 33 - - - 38214 RMVar_ID_38214 Human_SNP_ID_693844690 A-to-I Human chr21 + 34388889 34388889 34388889 CGGGAGTTTGAGACCAGCCTGGCCAACATGGTAAAATCCTGTCTCTACTAAAAATATAAAAATTA CGGGAGTTTGAGACCAGCCTGGCCAACATGGTGAAATCCTGTCTCTACTAAAAATATAAAAATTA A G SMIM11A Ensembl:ENSG00000205670 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1370230330 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_361030 38215 RMVar_ID_38215 Human_SNP_ID_693844695 A-to-I Human chr21 + 34388921 34388921 34388921 AAAATCCTGTCTCTACTAAAAATATAAAAATTAGCCAGGTGTAGTGGCGCGCGTCTGTAATCCCA AAAATCCTGTCTCTACTAAAAATATAAAAATTGGCCAGGTGTAGTGGCGCGCGTCTGTAATCCCA A G SMIM11A Ensembl:ENSG00000205670 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1386227027 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_571766 RMVar_hsa_circ_361030 38216 RMVar_ID_38216 Human_SNP_ID_693846142 A-to-I Human chr21 + 34398633 34398632 34398634 CTTTCTTTCTCCTTTTCTTTTCTTTTTGAGACAGAGTCTGACTCTGTTACCCAGGTTGGAGCGCA CTTTCTTTCTCCTTTTCTTTTCTTTTTGAGAC__AGTCTGACTCTGTTACCCAGGTTGGAGCGCA CAG C SMIM11A Ensembl:ENSG00000205670 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs955951543 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_361030 38217 RMVar_ID_38217 Human_SNP_ID_693887612 A-to-I Human chr21 - 34610642 34610642 34610642 GGAATCGCCTGGAAAGCTCCCCAGGTGATTCTAATTGTTAGCTGAGGTTGGGAACCATTGTCTGA GGAATCGCCTGGAAAGCTCCCCAGGTGATTCTGATTGTTAGCTGAGGTTGGGAACCATTGTCTGA T C RCAN1 Ensembl:ENSG00000159200 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1470028770 Functional Loss SNV dbSNP153 33..33 33 - - - 38218 RMVar_ID_38218 Human_SNP_ID_693934159 A-to-I Human chr21 - 34794857 34794857 34794857 GAGTTGTCACAAGAGGGGCGGGCGATGCTACTAACACCTAATGGGTAAAGCAGAGATGCTGCCAC GAGTTGTCACAAGAGGGGCGGGCGATGCTACTGACACCTAATGGGTAAAGCAGAGATGCTGCCAC T C RUNX1 Ensembl:ENSG00000159216 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs113833143 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_211970,RMVar_hsa_circ_105995,RMVar_hsa_circ_76660,RMVar_hsa_circ_211971 38219 RMVar_ID_38219 Human_SNP_ID_694239333 A-to-I Human chr21 - 36050705 36050705 36050705 TTATCTCGAGCCAAGAAAACAGCTTTACCTCTATGACCCCGCGTATTCTTTACTACCATTGGGAA TTATCTCGAGCCAAGAAAACAGCTTTACCTCTGTGACCCCGCGTATTCTTTACTACCATTGGGAA T C SETD4 Ensembl:ENSG00000185917 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1395637836 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114584,RMVar_hsa_circ_211978,RMVar_hsa_circ_43052,RMVar_hsa_circ_88990,RMVar_hsa_circ_125722,RMVar_hsa_circ_211980,RMVar_hsa_circ_211982 38220 RMVar_ID_38220 Human_SNP_ID_694259308 A-to-I Human chr21 - 36129751 36129747 36129752 GTTGACCAGGCTGGTCTCGAAGTCCTGACCTCAAGCACTCTGCCTGCCTTGGCCTTCCAAAATGC GTTGACCAGGCTGGTCTCGAAGTCCTGACCT_____ACTCTGCCTGCCTTGGCCTTCCAAAATGC TGCTTG T CBR3-AS1,CBR3-AS1:2,CBR3-AS1:3,CBR3-AS1:4,CBR3-AS1:5 RNACentral:URS0000D5AFF8,RNACentral:URS0000D586A4,RNACentral:URS0000D58471,RNACentral:URS0000D574DC,RNACentral:URS0000D5E271 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1199167961 Functional Loss DEL dbSNP153 32..36 33 - - - 38221 RMVar_ID_38221 Human_SNP_ID_694260000 A-to-I Human chr21 - 36132570 36132570 36132570 GACCAGGGTAAATTTGACCCTCCAGACCTCACATTTGTTCTGGAGCCCATACTCACCAATCAGCT GACCAGGGTAAATTTGACCCTCCAGACCTCACGTTTGTTCTGGAGCCCATACTCACCAATCAGCT T C CBR3-AS1 Ensembl:ENSG00000236830 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1340715162 Functional Loss SNV dbSNP153 33..33 33 - - - 38222 RMVar_ID_38222 Human_SNP_ID_694313307 A-to-I Human chr21 + 36326379 36326379 36326379 AACCCCATCTTTACCAAAAATAAAAAAAAATTAGCCGGGCATGGTGACACACAACCGTGGTCCCA AACCCCATCTTTACCAAAAATAAAAAAAAATTCGCCGGGCATGGTGACACACAACCGTGGTCCCA A C MORC3 Ensembl:ENSG00000159256 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1024513499 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_212031,RMVar_hsa_circ_212032,RMVar_hsa_circ_122315,RMVar_hsa_circ_212041 38223 RMVar_ID_38223 Human_SNP_ID_694319013 A-to-I Human chr21 + 36346239 36346238 36346239 GACGGCTTTACCATGTTGACCAGGCTGGCCTCAAACTCCTGAACTCAAGTGATCCACCCACGTCG GACGGCTTTACCATGTTGACCAGGCTGGCCTC_AACTCCTGAACTCAAGTGATCCACCCACGTCG CA C MORC3 Ensembl:ENSG00000159256 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs534262709 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_14277446 RMVar_hsa_circ_90406,RMVar_hsa_circ_119213,RMVar_hsa_circ_321448,RMVar_hsa_circ_351725,RMVar_hsa_circ_359436,RMVar_hsa_circ_281141,RMVar_hsa_circ_64823,RMVar_hsa_circ_212046,RMVar_hsa_circ_212047,RMVar_hsa_circ_212045,RMVar_hsa_circ_108501,RMVar_hsa_circ_212048,RMVar_hsa_circ_122779,RMVar_hsa_circ_106448,RMVar_hsa_circ_99382,RMVar_hsa_circ_212056,RMVar_hsa_circ_212058,RMVar_hsa_circ_84832,RMVar_hsa_circ_212059,RMVar_hsa_circ_212057,RMVar_hsa_circ_212055,RMVar_hsa_circ_212065,RMVar_hsa_circ_365589,RMVar_hsa_circ_307657,RMVar_hsa_circ_351165,RMVar_hsa_circ_45405,RMVar_hsa_circ_297917,RMVar_hsa_circ_212066,RMVar_hsa_circ_212067 38224 RMVar_ID_38224 Human_SNP_ID_694325730 A-to-I Human chr21 + 36370858 36370857 36370859 GCCCGGCTAATTTTTGTCTTTTTATTAGAGACAGGGTTTCACCACATTGGCCAGGCTGATCTCAA GCCCGGCTAATTTTTGTCTTTTTATTAGAGAC__GGTTTCACCACATTGGCCAGGCTGATCTCAA CAG C MORC3 Ensembl:ENSG00000159256 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1201202880 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_321448,RMVar_hsa_circ_212047,RMVar_hsa_circ_122779,RMVar_hsa_circ_212059,RMVar_hsa_circ_41839,RMVar_hsa_circ_338713,RMVar_hsa_circ_212071,RMVar_hsa_circ_296802,RMVar_hsa_circ_212077,RMVar_hsa_circ_321504,RMVar_hsa_circ_212073,RMVar_hsa_circ_212078,RMVar_hsa_circ_324964 38225 RMVar_ID_38225 Human_SNP_ID_694325731 A-to-I Human chr21 + 36370858 36370858 36370858 GCCCGGCTAATTTTTGTCTTTTTATTAGAGACAGGGTTTCACCACATTGGCCAGGCTGATCTCAA GCCCGGCTAATTTTTGTCTTTTTATTAGAGACGGGGTTTCACCACATTGGCCAGGCTGATCTCAA A G MORC3 Ensembl:ENSG00000159256 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1040119593 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_321448,RMVar_hsa_circ_212047,RMVar_hsa_circ_122779,RMVar_hsa_circ_212059,RMVar_hsa_circ_41839,RMVar_hsa_circ_338713,RMVar_hsa_circ_212071,RMVar_hsa_circ_296802,RMVar_hsa_circ_212077,RMVar_hsa_circ_321504,RMVar_hsa_circ_212073,RMVar_hsa_circ_212078,RMVar_hsa_circ_324964 38226 RMVar_ID_38226 Human_SNP_ID_694326747 A-to-I Human chr21 + 36374855 36374855 36374855 ACCAAGCCCGGCTAATATTTTGTGTTTTTAGTAGAGTCAGGGTTTCACCATGTTGGCCAGGCTGG ACCAAGCCCGGCTAATATTTTGTGTTTTTAGTTGAGTCAGGGTTTCACCATGTTGGCCAGGCTGG A T MORC3 Ensembl:ENSG00000159256 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs934559890 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122779,RMVar_hsa_circ_212059,RMVar_hsa_circ_212079 38227 RMVar_ID_38227 Human_SNP_ID_694334418 A-to-I Human chr21 + 36401975 36401975 36401975 GTTGGCCAGGCTGGTCTCGTACTCCTGGACTCAAGTGATCCGCCCGCCTTGGCCTCCCAAAGTGC GTTGGCCAGGCTGGTCTCGTACTCCTGGACTCCAGTGATCCGCCCGCCTTGGCCTCCCAAAGTGC A C CHAF1B Ensembl:ENSG00000159259 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1325712607 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14278933 RMVar_hsa_circ_78110,RMVar_hsa_circ_63319,RMVar_hsa_circ_212080,RMVar_hsa_circ_345282,RMVar_hsa_circ_296352,RMVar_hsa_circ_374472,RMVar_hsa_circ_267686,RMVar_hsa_circ_343799,RMVar_hsa_circ_212082,RMVar_hsa_circ_339139,RMVar_hsa_circ_369434,RMVar_hsa_circ_119449,RMVar_hsa_circ_11578,RMVar_hsa_circ_212085,RMVar_hsa_circ_32709,RMVar_hsa_circ_212086,RMVar_hsa_circ_212084,RMVar_hsa_circ_330148 38228 RMVar_ID_38228 Human_SNP_ID_694338329 A-to-I Human chr21 + 36417361 36417361 36417361 TTTTTTTTCTTTTTTTTTTGAGATGGAGTCTCACTCTGTCGCCCAGGCTGGAGTACAGTGGCACA TTTTTTTTCTTTTTTTTTTGAGATGGAGTCTCGCTCTGTCGCCCAGGCTGGAGTACAGTGGCACA A G CHAF1B Ensembl:ENSG00000159259 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1227544337 Functional Loss SNV dbSNP153 33..33 33 - - - 38229 RMVar_ID_38229 Human_SNP_ID_694338334 A-to-I Human chr21 + 36417393 36417393 36417393 ACTCTGTCGCCCAGGCTGGAGTACAGTGGCACAATCTCGGCTCACTATAACCTCCGCCTCCTGGG ACTCTGTCGCCCAGGCTGGAGTACAGTGGCACCATCTCGGCTCACTATAACCTCCGCCTCCTGGG A C CHAF1B Ensembl:ENSG00000159259 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1377751303 Functional Loss SNV dbSNP153 33..33 33 - - - 38230 RMVar_ID_38230 Human_SNP_ID_694338337 A-to-I Human chr21 + 36417404 36417404 36417404 CAGGCTGGAGTACAGTGGCACAATCTCGGCTCACTATAACCTCCGCCTCCTGGGTTCAAACGATT CAGGCTGGAGTACAGTGGCACAATCTCGGCTCTCTATAACCTCCGCCTCCTGGGTTCAAACGATT A T CHAF1B Ensembl:ENSG00000159259 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1424340498 Functional Loss SNV dbSNP153 33..33 33 - - - 38231 RMVar_ID_38231 Human_SNP_ID_694338354 A-to-I Human chr21 + 36417463 36417463 36417463 ACGATTCTCCTGCCTCTGCCTCTTGAGTAGCTAGGATTACAGGTGTGTGCCACCACATCCGGCTA ACGATTCTCCTGCCTCTGCCTCTTGAGTAGCTGGGATTACAGGTGTGTGCCACCACATCCGGCTA A G CHAF1B Ensembl:ENSG00000159259 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1242448458 Functional Loss SNV dbSNP153 33..33 33 - - - 38232 RMVar_ID_38232 Human_SNP_ID_694338362 A-to-I Human chr21 + 36417495 36417495 36417495 AGGATTACAGGTGTGTGCCACCACATCCGGCTAATTTTTATATTTTTAGTAGAGATGGGGTTTTG AGGATTACAGGTGTGTGCCACCACATCCGGCTCATTTTTATATTTTTAGTAGAGATGGGGTTTTG A C CHAF1B Ensembl:ENSG00000159259 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs542897476 Functional Loss SNV dbSNP153 33..33 33 - - - 38233 RMVar_ID_38233 Human_SNP_ID_694338376 A-to-I Human chr21 + 36417539 36417539 36417539 TTTAGTAGAGATGGGGTTTTGCCATGTTGGCCAAGCTGGTCTCTAACTCCTGACCTCAGATGATC TTTAGTAGAGATGGGGTTTTGCCATGTTGGCCGAGCTGGTCTCTAACTCCTGACCTCAGATGATC A G CHAF1B Ensembl:ENSG00000159259 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs962893701 Functional Loss SNV dbSNP153 33..33 33 - - - 38234 RMVar_ID_38234 Human_SNP_ID_694338390 A-to-I Human chr21 + 36417591 36417591 36417591 ACCTCAGATGATCTGCCTGCCTCGGCCTCCCAAAGTGTTGGGATTACAGGTGTGAGCTACTGCAC ACCTCAGATGATCTGCCTGCCTCGGCCTCCCAGAGTGTTGGGATTACAGGTGTGAGCTACTGCAC A G CHAF1B Ensembl:ENSG00000159259 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs190149225 Functional Loss SNV dbSNP153 33..33 33 - - - 38235 RMVar_ID_38235 Human_SNP_ID_694360923 A-to-I Human chr21 - 36504218 36504218 36504218 CTTTTACCTCAGCCTCACAAGTAGCTGGGACTACAGGCGTGCACCACCATGCCCAGGTAATTTTT CTTTTACCTCAGCCTCACAAGTAGCTGGGACTGCAGGCGTGCACCACCATGCCCAGGTAATTTTT T C CLDN14 Ensembl:ENSG00000159261 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1194724131 Functional Loss SNV dbSNP153 33..33 33 - - - 38236 RMVar_ID_38236 Human_SNP_ID_694360925 A-to-I Human chr21 - 36504231 36504231 36504231 GGCTTAAGTGATCCTTTTACCTCAGCCTCACAAGTAGCTGGGACTACAGGCGTGCACCACCATGC GGCTTAAGTGATCCTTTTACCTCAGCCTCACAGGTAGCTGGGACTACAGGCGTGCACCACCATGC T C CLDN14 Ensembl:ENSG00000159261 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1252635122 Functional Loss SNV dbSNP153 33..33 33 - - - 38237 RMVar_ID_38237 Human_SNP_ID_694429921 A-to-I Human chr21 - 36770747 36770747 36770747 GGCTCTACCAAACCCTGTCTCTACCAAAAAATACAAAAATTAGCCAGGTGTGGTGGTATGAACCC GGCTCTACCAAACCCTGTCTCTACCAAAAAATGCAAAAATTAGCCAGGTGTGGTGGTATGAACCC T C HLCS Ensembl:ENSG00000159267 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1000080455 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38828,RMVar_hsa_circ_212099,RMVar_hsa_circ_39806 38238 RMVar_ID_38238 Human_SNP_ID_694444718 A-to-I Human chr21 - 36833123 36833123 36833123 CCAGCAGGTTGGGAAGCTGAGCTGGGAGGATCACTTGAGCCTGGGAAGTCAAGGCTGCTATGGAC CCAGCAGGTTGGGAAGCTGAGCTGGGAGGATCGCTTGAGCCTGGGAAGTCAAGGCTGCTATGGAC T C HLCS Ensembl:ENSG00000159267 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264010912 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17572453 RMVar_hsa_circ_38828,RMVar_hsa_circ_39806 38239 RMVar_ID_38239 Human_SNP_ID_694444730 A-to-I Human chr21 - 36833185 36833184 36833185 CATCTCTACTAAAATTAAAAAAAAAAAAATTTAGCTAGGCATGGTGGCATGTGCCTGTAGTCCCA CATCTCTACTAAAATTAAAAAAAAAAAAATTT_GCTAGGCATGGTGGCATGTGCCTGTAGTCCCA CT C HLCS Ensembl:ENSG00000159267 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1340527993 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_38828,RMVar_hsa_circ_39806 38240 RMVar_ID_38240 Human_SNP_ID_694444731 A-to-I Human chr21 - 36833185 36833185 36833185 CATCTCTACTAAAATTAAAAAAAAAAAAATTTAGCTAGGCATGGTGGCATGTGCCTGTAGTCCCA CATCTCTACTAAAATTAAAAAAAAAAAAATTTTGCTAGGCATGGTGGCATGTGCCTGTAGTCCCA T A HLCS Ensembl:ENSG00000159267 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1299536039 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38828,RMVar_hsa_circ_39806 38241 RMVar_ID_38241 Human_SNP_ID_694444732 A-to-I Human chr21 - 36833185 36833185 36833185 CATCTCTACTAAAATTAAAAAAAAAAAAATTTAGCTAGGCATGGTGGCATGTGCCTGTAGTCCCA CATCTCTACTAAAATTAAAAAAAAAAAAATTTGGCTAGGCATGGTGGCATGTGCCTGTAGTCCCA T C HLCS Ensembl:ENSG00000159267 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1299536039 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38828,RMVar_hsa_circ_39806 38242 RMVar_ID_38242 Human_SNP_ID_694453919 A-to-I Human chr21 - 36871773 36871773 36871773 TTGGGGTACTTGTCATTTTATTATTGAGTTGTAGAAGTTCTTTGTATATCTCAGATACCAGTCCT TTGGGGTACTTGTCATTTTATTATTGAGTTGTGGAAGTTCTTTGTATATCTCAGATACCAGTCCT T C HLCS Ensembl:ENSG00000159267 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1569127747 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38828,RMVar_hsa_circ_39806 38243 RMVar_ID_38243 Human_SNP_ID_694454225 A-to-I Human chr21 - 36873039 36873039 36873039 TTTTCAGGAAAATGCAGATTAAAAGCACAGTGAGATACCACTGCATATCCCCCAGATCAGCTGAA TTTTCAGGAAAATGCAGATTAAAAGCACAGTGCGATACCACTGCATATCCCCCAGATCAGCTGAA T G HLCS Ensembl:ENSG00000159267 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1292136957 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38828,RMVar_hsa_circ_39806 38244 RMVar_ID_38244 Human_SNP_ID_694476440 A-to-I Human chr21 - 36962544 36962544 36962544 GGCTCAAGCGATCTGCCCACCTTGGCCTCCCAAAGTGCTAGGATTACAGGCGTGAGCCACTGTGC GGCTCAAGCGATCTGCCCACCTTGGCCTCCCAGAGTGCTAGGATTACAGGCGTGAGCCACTGTGC T C HLCS Ensembl:ENSG00000159267 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs942491385 Functional Loss SNV dbSNP153 33..33 33 - - - 38245 RMVar_ID_38245 Human_SNP_ID_694477225 A-to-I Human chr21 - 36965766 36965766 36965766 GATTGAGCCATTGCACTCCAGTCTGGGTGACAAAGCAAGACCCTGTCTTAAGAAAAAAAAAAAAA GATTGAGCCATTGCACTCCAGTCTGGGTGACAGAGCAAGACCCTGTCTTAAGAAAAAAAAAAAAA T C HLCS Ensembl:ENSG00000159267 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs558990807 Functional Loss SNV dbSNP153 33..33 33 - - - 38246 RMVar_ID_38246 Human_SNP_ID_694478369 A-to-I Human chr21 + 36969599 36969598 36969600 ACCACAGACTAGGGATTTTTTTTTTTTTTTTTAGATGAAGTCTCACTTGCCCAGGTTGGAGTGCA ACCACAGACTAGGGATTTTTTTTTTTTTTTTT__ATGAAGTCTCACTTGCCCAGGTTGGAGTGCA TAG T AP000704.2 Ensembl:ENSG00000224790 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1360605380 Functional Loss DEL dbSNP153 33..34 33 - - - Human_Splice_Rec_2119907 38247 RMVar_ID_38247 Human_SNP_ID_694478370 A-to-I Human chr21 + 36969599 36969598 36969599 ACCACAGACTAGGGATTTTTTTTTTTTTTTTTAGATGAAGTCTCACTTGCCCAGGTTGGAGTGCA ACCACAGACTAGGGATTTTTTTTTTTTTTTTT_GATGAAGTCTCACTTGCCCAGGTTGGAGTGCA TA T AP000704.2 Ensembl:ENSG00000224790 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1419087251 Functional Loss DEL dbSNP153 33..33 33 - - - Human_Splice_Rec_2119907 38248 RMVar_ID_38248 Human_SNP_ID_694478371 A-to-I Human chr21 + 36969599 36969599 36969599 ACCACAGACTAGGGATTTTTTTTTTTTTTTTTAGATGAAGTCTCACTTGCCCAGGTTGGAGTGCA ACCACAGACTAGGGATTTTTTTTTTTTTTTTTCGATGAAGTCTCACTTGCCCAGGTTGGAGTGCA A C AP000704.2 Ensembl:ENSG00000224790 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1393827083 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2119907 38249 RMVar_ID_38249 Human_SNP_ID_694478372 A-to-I Human chr21 + 36969599 36969599 36969599 ACCACAGACTAGGGATTTTTTTTTTTTTTTTTAGATGAAGTCTCACTTGCCCAGGTTGGAGTGCA ACCACAGACTAGGGATTTTTTTTTTTTTTTTTTGATGAAGTCTCACTTGCCCAGGTTGGAGTGCA A T AP000704.2 Ensembl:ENSG00000224790 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1393827083 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2119907 38250 RMVar_ID_38250 Human_SNP_ID_694478388 A-to-I Human chr21 + 36969642 36969642 36969642 CACTTGCCCAGGTTGGAGTGCAGCGCGATCTCAGCTCACTGCAACGTCCGCCTCCCAAGTTCAAG CACTTGCCCAGGTTGGAGTGCAGCGCGATCTCGGCTCACTGCAACGTCCGCCTCCCAAGTTCAAG A G AP000704.2 Ensembl:ENSG00000224790 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1290334988 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2119906 38251 RMVar_ID_38251 Human_SNP_ID_694478629 A-to-I Human chr21 + 36970721 36970721 36970721 AAGGAACTATGTAGAAAATCTTCGCCGGGCACAGTGGCTCACGCCTATAATCCCAGCACTTTGGG AAGGAACTATGTAGAAAATCTTCGCCGGGCACGGTGGCTCACGCCTATAATCCCAGCACTTTGGG A G AP000704.2 Ensembl:ENSG00000224790 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs533561540 Functional Loss SNV dbSNP153 33..33 33 - - - 38252 RMVar_ID_38252 Human_SNP_ID_694478632 A-to-I Human chr21 + 36970737 36970737 36970737 AATCTTCGCCGGGCACAGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCCAAGATGGGCAG AATCTTCGCCGGGCACAGTGGCTCACGCCTATTATCCCAGCACTTTGGGAGGCCAAGATGGGCAG A T AP000704.2 Ensembl:ENSG00000224790 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1233630938 Functional Loss SNV dbSNP153 33..33 33 - - - 38253 RMVar_ID_38253 Human_SNP_ID_694544156 A-to-I Human chr21 - 37228827 37228827 37228827 GGGTCTTGCTGTGTTACACAGGCTGTTCTTGAACTCCTGGCCTCAAGTGATCCTCCTGCCTTTGC GGGTCTTGCTGTGTTACACAGGCTGTTCTTGAGCTCCTGGCCTCAAGTGATCCTCCTGCCTTTGC T C VPS26C Ensembl:ENSG00000157538 Protein coding exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1208244954 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1937,RMVar_hsa_circ_91156,RMVar_hsa_circ_22708,RMVar_hsa_circ_212159 38254 RMVar_ID_38254 Human_SNP_ID_694580612 A-to-I Human chr21 + 37372341 37372341 37372341 TGTGTTAGTGCCACCTGTAGTCCAGGCTACTCAGGAGACTGAGGTGGGAGGATCAGTTGAGCCTG TGTGTTAGTGCCACCTGTAGTCCAGGCTACTCGGGAGACTGAGGTGGGAGGATCAGTTGAGCCTG A G DYRK1A Ensembl:ENSG00000157540 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs942150058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14290438 RMVar_hsa_circ_112754,RMVar_hsa_circ_212162 38255 RMVar_ID_38255 Human_SNP_ID_694581641 A-to-I Human chr21 + 37375724 37375724 37375724 TTTTTTGTTATTTTTAGTAGAGACGGGATTTCACTATGTTGGTCAGACTGGTCTCCAACTCCTGA TTTTTTGTTATTTTTAGTAGAGACGGGATTTCTCTATGTTGGTCAGACTGGTCTCCAACTCCTGA A T DYRK1A Ensembl:ENSG00000157540 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1391560948 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14290698 RMVar_hsa_circ_112754,RMVar_hsa_circ_212162,RMVar_hsa_circ_212164,RMVar_hsa_circ_212165 38256 RMVar_ID_38256 Human_SNP_ID_694581823 A-to-I Human chr21 + 37376338 37376338 37376338 GAGACCAGCCTGGCTAAAATGGTGAAACCCCCATCTCTACTACAGATACAGAAATTAGCCAGGTG GAGACCAGCCTGGCTAAAATGGTGAAACCCCCTTCTCTACTACAGATACAGAAATTAGCCAGGTG A T DYRK1A Ensembl:ENSG00000157540 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs528488220 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112754,RMVar_hsa_circ_212162,RMVar_hsa_circ_212164,RMVar_hsa_circ_212165 38257 RMVar_ID_38257 Human_SNP_ID_694581826 A-to-I Human chr21 + 37376344 37376344 37376344 AGCCTGGCTAAAATGGTGAAACCCCCATCTCTACTACAGATACAGAAATTAGCCAGGTGCAGTAG AGCCTGGCTAAAATGGTGAAACCCCCATCTCTGCTACAGATACAGAAATTAGCCAGGTGCAGTAG A G DYRK1A Ensembl:ENSG00000157540 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs945727762 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112754,RMVar_hsa_circ_212162,RMVar_hsa_circ_212164,RMVar_hsa_circ_212165 38258 RMVar_ID_38258 Human_SNP_ID_694591566 A-to-I Human chr21 + 37410605 37410605 37410605 GAAGTGCAGTGGCACGATCATAGGTGGTCACTACAGTCTCAGATTCCTGGGCTTAAGCAGTCTTC GAAGTGCAGTGGCACGATCATAGGTGGTCACTGCAGTCTCAGATTCCTGGGCTTAAGCAGTCTTC A G DYRK1A Ensembl:ENSG00000157540 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264231393 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2121114,Human_Splice_Rec_2121115 RMVar_hsa_circ_5942,RMVar_hsa_circ_112754,RMVar_hsa_circ_212162,RMVar_hsa_circ_212164,RMVar_hsa_circ_212165 38259 RMVar_ID_38259 Human_SNP_ID_694598682 A-to-I Human chr21 + 37437375 37437375 37437375 GAGTTGCCATCATCTAAAACGAGATATGTTGTAGGAGAAGCAGATTTTTTTGTGGAGTGGAGGGA GAGTTGCCATCATCTAAAACGAGATATGTTGTGGGAGAAGCAGATTTTTTTGTGGAGTGGAGGGA A G DYRK1A Ensembl:ENSG00000157540 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1322128738 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14295174 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 38260 RMVar_ID_38260 Human_SNP_ID_695020105 A-to-I Human chr21 + 39171529 39171529 39171529 CATGGACGAAGTGGTGTGGAGAAAGCAAGCTCACACTGTCGCTGCCTGTGCTGTACCTGTCCTGA CATGGACGAAGTGGTGTGGAGAAAGCAAGCTCGCACTGTCGCTGCCTGTGCTGTACCTGTCCTGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1023594253 Functional Loss SNV dbSNP153 33..33 33 - - - 38261 RMVar_ID_38261 Human_SNP_ID_695032315 A-to-I Human chr21 - 39217233 39217233 39217233 AAATTAGCCAGGCACGGTGGCACGTGCCTGTAATCGCAGGTACTTGGGAGGCTGAGGCAGGAGAA AAATTAGCCAGGCACGGTGGCACGTGCCTGTAGTCGCAGGTACTTGGGAGGCTGAGGCAGGAGAA T C BRWD1-IT1,BRWD1 Ensembl:ENSG00000237373,Ensembl:ENSG00000185658 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1476784224 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14306421 RMVar_hsa_circ_61354,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_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_212210,RMVar_hsa_circ_212211,RMVar_hsa_circ_271335,RMVar_hsa_circ_37322,RMVar_hsa_circ_212213,RMVar_hsa_circ_301937,RMVar_hsa_circ_369507,RMVar_hsa_circ_282755,RMVar_hsa_circ_43414,RMVar_hsa_circ_265554,RMVar_hsa_circ_102191,RMVar_hsa_circ_21888,RMVar_hsa_circ_23759,RMVar_hsa_circ_14397,RMVar_hsa_circ_212220,RMVar_hsa_circ_212215,RMVar_hsa_circ_212216,RMVar_hsa_circ_212214,RMVar_hsa_circ_319791,RMVar_hsa_circ_301372,RMVar_hsa_circ_294675,RMVar_hsa_circ_74485,RMVar_hsa_circ_41374,RMVar_hsa_circ_1124,RMVar_hsa_circ_125454,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_316350,RMVar_hsa_circ_38162,RMVar_hsa_circ_212227,RMVar_hsa_circ_52117,RMVar_hsa_circ_328258,RMVar_hsa_circ_344199,RMVar_hsa_circ_322141,RMVar_hsa_circ_278006,RMVar_hsa_circ_41342,RMVar_hsa_circ_38432,RMVar_hsa_circ_212228,RMVar_hsa_circ_212230,RMVar_hsa_circ_212231,RMVar_hsa_circ_212229,RMVar_hsa_circ_270056,RMVar_hsa_circ_297655,RMVar_hsa_circ_362682,RMVar_hsa_circ_366666,RMVar_hsa_circ_367204,RMVar_hsa_circ_305140,RMVar_hsa_circ_271256,RMVar_hsa_circ_66793,RMVar_hsa_circ_67192,RMVar_hsa_circ_58612,RMVar_hsa_circ_212234,RMVar_hsa_circ_212236,RMVar_hsa_circ_212237,RMVar_hsa_circ_212238,RMVar_hsa_circ_212235,RMVar_hsa_circ_212233 38262 RMVar_ID_38262 Human_SNP_ID_695046574 A-to-I Human chr21 - 39272415 39272415 39272415 TCATGCCGTTCTCCTGCCTCAGCCTCACGAGTAGCTGAGACTACAGGCGCCCGCCACATGCCCGG TCATGCCGTTCTCCTGCCTCAGCCTCACGAGTCGCTGAGACTACAGGCGCCCGCCACATGCCCGG T G BRWD1 Ensembl:ENSG00000185658 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1463264299 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25644551 RMVar_hsa_circ_40,RMVar_hsa_circ_61354,RMVar_hsa_circ_28646,RMVar_hsa_circ_49529,RMVar_hsa_circ_15558,RMVar_hsa_circ_212207,RMVar_hsa_circ_50555,RMVar_hsa_circ_29494,RMVar_hsa_circ_369507,RMVar_hsa_circ_102191,RMVar_hsa_circ_23759,RMVar_hsa_circ_212214,RMVar_hsa_circ_74485,RMVar_hsa_circ_41374,RMVar_hsa_circ_1124,RMVar_hsa_circ_212226,RMVar_hsa_circ_328258,RMVar_hsa_circ_212228,RMVar_hsa_circ_297655,RMVar_hsa_circ_367204,RMVar_hsa_circ_212237,RMVar_hsa_circ_212238,RMVar_hsa_circ_359939,RMVar_hsa_circ_103968,RMVar_hsa_circ_64445,RMVar_hsa_circ_212240,RMVar_hsa_circ_44808,RMVar_hsa_circ_86056,RMVar_hsa_circ_212239,RMVar_hsa_circ_212247,RMVar_hsa_circ_351657,RMVar_hsa_circ_293629,RMVar_hsa_circ_115060,RMVar_hsa_circ_108675,RMVar_hsa_circ_76712,RMVar_hsa_circ_78617,RMVar_hsa_circ_212248,RMVar_hsa_circ_212252,RMVar_hsa_circ_212250,RMVar_hsa_circ_212251,RMVar_hsa_circ_212249,RMVar_hsa_circ_12546,RMVar_hsa_circ_343864,RMVar_hsa_circ_89805,RMVar_hsa_circ_212267,RMVar_hsa_circ_212259,RMVar_hsa_circ_212260,RMVar_hsa_circ_106913,RMVar_hsa_circ_341775,RMVar_hsa_circ_83263,RMVar_hsa_circ_212268,RMVar_hsa_circ_358745,RMVar_hsa_circ_212266,RMVar_hsa_circ_212269,RMVar_hsa_circ_378742,RMVar_hsa_circ_338186,RMVar_hsa_circ_340211,RMVar_hsa_circ_24253,RMVar_hsa_circ_212270,RMVar_hsa_circ_212271,RMVar_hsa_circ_59530,RMVar_hsa_circ_102291,RMVar_hsa_circ_212278,RMVar_hsa_circ_367236,RMVar_hsa_circ_41814,RMVar_hsa_circ_67461,RMVar_hsa_circ_308850,RMVar_hsa_circ_315027,RMVar_hsa_circ_212279,RMVar_hsa_circ_339206,RMVar_hsa_circ_305887,RMVar_hsa_circ_20666,RMVar_hsa_circ_54716,RMVar_hsa_circ_212284,RMVar_hsa_circ_212285,RMVar_hsa_circ_212283,RMVar_hsa_circ_356279,RMVar_hsa_circ_361902,RMVar_hsa_circ_52058,RMVar_hsa_circ_212287,RMVar_hsa_circ_58941,RMVar_hsa_circ_212286,RMVar_hsa_circ_327879,RMVar_hsa_circ_366346,RMVar_hsa_circ_212288,RMVar_hsa_circ_273975,RMVar_hsa_circ_333288,RMVar_hsa_circ_341438,RMVar_hsa_circ_304616,RMVar_hsa_circ_212290,RMVar_hsa_circ_212291,RMVar_hsa_circ_378280,RMVar_hsa_circ_309252,RMVar_hsa_circ_286170,RMVar_hsa_circ_301704,RMVar_hsa_circ_11731,RMVar_hsa_circ_212292,RMVar_hsa_circ_212294,RMVar_hsa_circ_212295,RMVar_hsa_circ_212296,RMVar_hsa_circ_212293,RMVar_hsa_circ_27264,RMVar_hsa_circ_282273,RMVar_hsa_circ_308755,RMVar_hsa_circ_361507,RMVar_hsa_circ_329441,RMVar_hsa_circ_56305,RMVar_hsa_circ_212298,RMVar_hsa_circ_27095,RMVar_hsa_circ_212299,RMVar_hsa_circ_212297,RMVar_hsa_circ_361279,RMVar_hsa_circ_212301 38263 RMVar_ID_38263 Human_SNP_ID_695054325 A-to-I Human chr21 - 39299906 39299906 39299906 ATGATCTTGGTTCACTGCAACCTCCGCCTCCCAGGTTCAAGTGATTTCATACCTCAGCCTCCTAA ATGATCTTGGTTCACTGCAACCTCCGCCTCCCGGGTTCAAGTGATTTCATACCTCAGCCTCCTAA T C BRWD1 Ensembl:ENSG00000185658 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs970263314 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102191,RMVar_hsa_circ_212226,RMVar_hsa_circ_108675,RMVar_hsa_circ_212248,RMVar_hsa_circ_56305,RMVar_hsa_circ_104168,RMVar_hsa_circ_212310 38264 RMVar_ID_38264 Human_SNP_ID_695055321 A-to-I Human chr21 - 39303334 39303334 39303334 TTGTAGTTTTAGTACAAATGGGGTTTCACCACATTTGCCAGGCTGGTCTTGAACTCCTGACCATT TTGTAGTTTTAGTACAAATGGGGTTTCACCACGTTTGCCAGGCTGGTCTTGAACTCCTGACCATT T C BRWD1 Ensembl:ENSG00000185658 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1033498599 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7048130,Human_RBP_ID_14310392 RMVar_hsa_circ_102191,RMVar_hsa_circ_212226,RMVar_hsa_circ_108675,RMVar_hsa_circ_212248,RMVar_hsa_circ_56305,RMVar_hsa_circ_104168,RMVar_hsa_circ_212310 38265 RMVar_ID_38265 Human_SNP_ID_695055323 A-to-I Human chr21 - 39303339 39303339 39303339 AATCTTTGTAGTTTTAGTACAAATGGGGTTTCACCACATTTGCCAGGCTGGTCTTGAACTCCTGA AATCTTTGTAGTTTTAGTACAAATGGGGTTTCGCCACATTTGCCAGGCTGGTCTTGAACTCCTGA T C BRWD1 Ensembl:ENSG00000185658 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs372226730 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7048130,Human_RBP_ID_14310395 RMVar_hsa_circ_102191,RMVar_hsa_circ_212226,RMVar_hsa_circ_108675,RMVar_hsa_circ_212248,RMVar_hsa_circ_56305,RMVar_hsa_circ_104168,RMVar_hsa_circ_212310 38266 RMVar_ID_38266 Human_SNP_ID_695055339 A-to-I Human chr21 - 39303397 39303397 39303397 CTCCTGCCTCAGCCTCTCAAGTAGCTGAGATTACAGTCACCTGCTACCATGCCCGGCTAATCTTT CTCCTGCCTCAGCCTCTCAAGTAGCTGAGATTGCAGTCACCTGCTACCATGCCCGGCTAATCTTT T C BRWD1 Ensembl:ENSG00000185658 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs990308194 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102191,RMVar_hsa_circ_212226,RMVar_hsa_circ_108675,RMVar_hsa_circ_212248,RMVar_hsa_circ_56305,RMVar_hsa_circ_104168,RMVar_hsa_circ_212310 38267 RMVar_ID_38267 Human_SNP_ID_695055450 A-to-I Human chr21 - 39303728 39303728 39303728 GCCTCAGCCTCCTGGGCTCAAGCCGTCTTCCAACCTTAGTCTCCTGAGTAGCTGGAACCACAGGC GCCTCAGCCTCCTGGGCTCAAGCCGTCTTCCAGCCTTAGTCTCCTGAGTAGCTGGAACCACAGGC T C BRWD1 Ensembl:ENSG00000185658 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs548207649 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14310417,Human_RBP_ID_18781266 RMVar_hsa_circ_102191,RMVar_hsa_circ_212226,RMVar_hsa_circ_108675,RMVar_hsa_circ_212248,RMVar_hsa_circ_56305,RMVar_hsa_circ_104168,RMVar_hsa_circ_212310 38268 RMVar_ID_38268 Human_SNP_ID_695055451 A-to-I Human chr21 - 39303728 39303728 39303728 GCCTCAGCCTCCTGGGCTCAAGCCGTCTTCCAACCTTAGTCTCCTGAGTAGCTGGAACCACAGGC GCCTCAGCCTCCTGGGCTCAAGCCGTCTTCCACCCTTAGTCTCCTGAGTAGCTGGAACCACAGGC T G BRWD1 Ensembl:ENSG00000185658 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs548207649 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14310417,Human_RBP_ID_18781266 RMVar_hsa_circ_102191,RMVar_hsa_circ_212226,RMVar_hsa_circ_108675,RMVar_hsa_circ_212248,RMVar_hsa_circ_56305,RMVar_hsa_circ_104168,RMVar_hsa_circ_212310 38269 RMVar_ID_38269 Human_SNP_ID_695056495 A-to-I Human chr21 - 39306965 39306965 39306965 CCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCACTTGAACCCAGGAGGCAGAGGTT CCTGTAATCCCAGCTACTTGGGAGGCTGAGGCGGGAGAATCACTTGAACCCAGGAGGCAGAGGTT T C BRWD1 Ensembl:ENSG00000185658 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048400315 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102191,RMVar_hsa_circ_212226,RMVar_hsa_circ_108675,RMVar_hsa_circ_212248,RMVar_hsa_circ_56305,RMVar_hsa_circ_104168,RMVar_hsa_circ_212310 38270 RMVar_ID_38270 Human_SNP_ID_695056886 A-to-I Human chr21 - 39308396 39308396 39308396 CTGACTGCAACCTCTGCCTCACAGGTTCATGCAGTTCTCCTGCCTCAGCCTCCTGAGTAGCTGGG CTGACTGCAACCTCTGCCTCACAGGTTCATGCGGTTCTCCTGCCTCAGCCTCCTGAGTAGCTGGG T C BRWD1 Ensembl:ENSG00000185658 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs993303311 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102191,RMVar_hsa_circ_212226,RMVar_hsa_circ_108675,RMVar_hsa_circ_212248,RMVar_hsa_circ_56305,RMVar_hsa_circ_104168,RMVar_hsa_circ_212310 38271 RMVar_ID_38271 Human_SNP_ID_695060194 A-to-I Human chr21 - 39315552 39315552 39315552 TCGGTTCACTGCAGCCTCCGCCTCCGGGGTTCAAGCGATTCTCCTGCCTCAGCCTCTCAAGTAGC TCGGTTCACTGCAGCCTCCGCCTCCGGGGTTCCAGCGATTCTCCTGCCTCAGCCTCTCAAGTAGC T G BRWD1 Ensembl:ENSG00000185658 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1472766222 Functional Loss SNV dbSNP153 33..33 33 - - - 38272 RMVar_ID_38272 Human_SNP_ID_695060524 A-to-I Human chr21 - 39316810 39316807 39316811 CCTCAGCCTCTTAAGTAGCTGGGGCTACAGGTACACACCTACCACCCCTGGCTATTTTTTATTTC CCTCAGCCTCTTAAGTAGCTGGGGCTACAGG____CACCTACCACCCCTGGCTATTTTTTATTTC GTGTA G BRWD1 Ensembl:ENSG00000185658 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1199587153 Functional Loss DEL dbSNP153 32..35 33 - - - 38273 RMVar_ID_38273 Human_SNP_ID_695069175 A-to-I Human chr21 - 39347441 39347441 39347441 AGTTTAGCACTGCAGTCATCAGAAGAGGCAAGATTAATTTCCTTGACATTGAGGAGTTGTTGGAT AGTTTAGCACTGCAGTCATCAGAAGAGGCAAGGTTAATTTCCTTGACATTGAGGAGTTGTTGGAT T C HMGN1 Ensembl:ENSG00000205581 Protein coding intron GSE100210;GSE99789 HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 29129909,29796672 RNA-Seq:(High) rs569644582 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_780601,Human_RBP_ID_1937442,Human_RBP_ID_9122951,Human_RBP_ID_10042602,Human_RBP_ID_14311651,Human_RBP_ID_25645085 Human_Splice_Rec_2122782,Human_Splice_Rec_2122783,Human_Splice_Rec_2122796,Human_Splice_Rec_2122797,Human_Splice_Rec_2122812,Human_Splice_Rec_2122813,Human_Splice_Rec_2122828,Human_Splice_Rec_2122829,Human_Splice_Rec_2122848,Human_Splice_Rec_2122849,Human_Splice_Rec_2122868,Human_Splice_Rec_2122869,Human_Splice_Rec_2122890,Human_Splice_Rec_2122891,Human_Splice_Rec_2122910,Human_Splice_Rec_2122911,Human_Splice_Rec_2122934,Human_Splice_Rec_2122935 Human_miRNA_ID_1755848 RMVar_hsa_circ_84499,RMVar_hsa_circ_212321 38274 RMVar_ID_38274 Human_SNP_ID_695082656 A-to-I Human chr21 + 39395011 39395011 39395011 CCCACCTTAGTCTCCTGAATAGTTAGGATCACAGTTGCACACCACCATGCCCAGCTAATTAAAAA CCCACCTTAGTCTCCTGAATAGTTAGGATCACGGTTGCACACCACCATGCCCAGCTAATTAAAAA A G GET1,GET1-SH3BGR Ensembl:ENSG00000182093,Ensembl:ENSG00000285815 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1356355649 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109042,RMVar_hsa_circ_212322,RMVar_hsa_circ_42153 38275 RMVar_ID_38275 Human_SNP_ID_695082816 A-to-I Human chr21 + 39395625 39395625 39395625 ACCTCAGGTGATCCACCTGCCTTATCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACTGTGC ACCTCAGGTGATCCACCTGCCTTATCCTCCCAGAGTGCTGGGATTACAGGTGTGAGCCACTGTGC A G GET1,GET1-SH3BGR Ensembl:ENSG00000182093,Ensembl:ENSG00000285815 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1326457532 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109042,RMVar_hsa_circ_212322,RMVar_hsa_circ_42153 38276 RMVar_ID_38276 Human_SNP_ID_695083380 A-to-I Human chr21 + 39397624 39397624 39397624 GTATTTAAAGCATTTTGAATGAAGTGTATTTTATAAGCATTTAATATTTATGCTCTTTAGAATGG GTATTTAAAGCATTTTGAATGAAGTGTATTTTGTAAGCATTTAATATTTATGCTCTTTAGAATGG A G GET1,GET1-SH3BGR Ensembl:ENSG00000182093,Ensembl:ENSG00000285815 Protein coding,Protein coding intron,intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs906701365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_572604,Human_RBP_ID_1604540,Human_RBP_ID_1937460,Human_RBP_ID_17979946,Human_RBP_ID_23927946 Human_miRNA_ID_145752,Human_miRNA_ID_855419,Human_miRNA_ID_994183,Human_miRNA_ID_2375556 RMVar_hsa_circ_109042,RMVar_hsa_circ_212322,RMVar_hsa_circ_42153 38277 RMVar_ID_38277 Human_SNP_ID_418756173 A-to-I Human chr10 + 141422 141422 141422 ACAATAAAATGTAAAGGCAAGAGGACTGCTTGAGCCCAGGAGTTTGAGGCTACAGTGAGCTAAAT ACAATAAAATGTAAAGGCAAGAGGACTGCTTGTGCCCAGGAGTTTGAGGCTACAGTGAGCTAAAT A T ZMYND11 Ensembl:ENSG00000015171 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs948379034 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5952285,Human_RBP_ID_11326281 38278 RMVar_ID_38278 Human_SNP_ID_418996321 A-to-I Human chr10 - 880493 880493 880493 TTCGTAGAGATGGGGTTTCGCCATGTTGCCCAAGCTGGTCTCGAACTCTGGCCTCAAGTGATCTG TTCGTAGAGATGGGGTTTCGCCATGTTGCCCATGCTGGTCTCGAACTCTGGCCTCAAGTGATCTG T A LARP4B Ensembl:ENSG00000107929 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs374551961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11456200 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_103415,RMVar_hsa_circ_141526,RMVar_hsa_circ_141527,RMVar_hsa_circ_83994,RMVar_hsa_circ_141530,RMVar_hsa_circ_141528,RMVar_hsa_circ_82505,RMVar_hsa_circ_286816,RMVar_hsa_circ_99469,RMVar_hsa_circ_141531,RMVar_hsa_circ_288999,RMVar_hsa_circ_141535,RMVar_hsa_circ_141536,RMVar_hsa_circ_82430,RMVar_hsa_circ_141537,RMVar_hsa_circ_280882,RMVar_hsa_circ_122334,RMVar_hsa_circ_141540,RMVar_hsa_circ_141541,RMVar_hsa_circ_316961,RMVar_hsa_circ_286634,RMVar_hsa_circ_307026 38279 RMVar_ID_38279 Human_SNP_ID_419002520 A-to-I Human chr10 - 904432 904432 904432 CTCTTAATTTAGCCTCCCAAGTTCCTGGGACTACAGGCACATGTCACCACACTTGACTAATTTTT CTCTTAATTTAGCCTCCCAAGTTCCTGGGACTGCAGGCACATGTCACCACACTTGACTAATTTTT T C LARP4B Ensembl:ENSG00000107929 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965929376 Functional Loss SNV dbSNP153 33..33 33 - - - 38280 RMVar_ID_38280 Human_SNP_ID_419006386 A-to-I Human chr10 - 916865 916863 916865 AGCAAGACCCCCATCTCGACAAAAAATAGAAAAATTAGCCAGGTGTGGTGGTGTGTGCTTATAGT AGCAAGACCCCCATCTCGACAAAAAATAGAAA__TTAGCCAGGTGTGGTGGTGTGTGCTTATAGT ATT A LARP4B Ensembl:ENSG00000107929 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1016344055 Functional Loss DEL dbSNP153 33..34 33 - - - 38281 RMVar_ID_38281 Human_SNP_ID_419009563 A-to-I Human chr10 - 928689 928689 928689 GTAGTCCAGCTGTTGGAGAAGCTGAAGTGGGAAGATCGCTTGAGCTTGGGAGGTTGAGGCTGCAG GTAGTCCAGCTGTTGGAGAAGCTGAAGTGGGAGGATCGCTTGAGCTTGGGAGGTTGAGGCTGCAG T C LARP4B Ensembl:ENSG00000107929 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1356215652 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8342574,Human_RBP_ID_11475012 38282 RMVar_ID_38282 Human_SNP_ID_419009583 A-to-I Human chr10 - 928781 928781 928781 GGAGCCCAGGAGTTCACCAGCCTGGGCAACATAGAGAGACCTCATCTCTACCAAAAAATCAAAAA GGAGCCCAGGAGTTCACCAGCCTGGGCAACATCGAGAGACCTCATCTCTACCAAAAAATCAAAAA T G LARP4B Ensembl:ENSG00000107929 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1055333166 Functional Loss SNV dbSNP153 33..33 33 - - - 38283 RMVar_ID_38283 Human_SNP_ID_419024121 A-to-I Human chr10 - 982223 982223 982223 GTTGGGCATAGTTACACGCACCTGTAGGCTGAAGCAGGAAAATTGCTTGAGGCAGGAGGTTGCAG GTTGGGCATAGTTACACGCACCTGTAGGCTGAGGCAGGAAAATTGCTTGAGGCAGGAGGTTGCAG T C AL359878.1 Ensembl:ENSG00000205740 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1479925652 Functional Loss SNV dbSNP153 33..33 33 - - - 38284 RMVar_ID_38284 Human_SNP_ID_419026038 A-to-I Human chr10 + 989254 989254 989254 CTCCTGCTTCAGCCTCCCGAGTAACAGGGATTACAGTCGTGCACCACCACACCCAGCTAATTTTC CTCCTGCTTCAGCCTCCCGAGTAACAGGGATTGCAGTCGTGCACCACCACACCCAGCTAATTTTC A G GTPBP4 Ensembl:ENSG00000107937 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1486012508 Functional Loss SNV dbSNP153 33..33 33 - - - 38285 RMVar_ID_38285 Human_SNP_ID_419026415 A-to-I Human chr10 + 990602 990602 990602 AAAATTAGCCAGGCGTGGTGGCGGGCGCCTGTAGTCCCAGCTGCTGGGGAGGCTGAGGCAGGAGA AAAATTAGCCAGGCGTGGTGGCGGGCGCCTGTGGTCCCAGCTGCTGGGGAGGCTGAGGCAGGAGA A G GTPBP4 Ensembl:ENSG00000107937 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1285612497 Functional Loss SNV dbSNP153 33..33 33 - - - 38286 RMVar_ID_38286 Human_SNP_ID_419028893 A-to-I Human chr10 + 999304 999303 999305 CCACGACCGGCCAATTTTTGTGTTTTTTTAGTAGAGAGGGGGTTTCACCATGTTGGCCAGGCTGG CCACGACCGGCCAATTTTTGTGTTTTTTTAGT__AGAGGGGGTTTCACCATGTTGGCCAGGCTGG TAG T GTPBP4 Ensembl:ENSG00000107937 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs995538425 Functional Loss DEL dbSNP153 33..34 33 - - - 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_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_141554,RMVar_hsa_circ_141555,RMVar_hsa_circ_141553 38287 RMVar_ID_38287 Human_SNP_ID_419028974 A-to-I Human chr10 + 999730 999730 999730 CCTGTAATCCCAACACTTTGGGAGGCCAAGGCAGGCAGCTAACCTGAGGTCAGAAGTTCGAGATT CCTGTAATCCCAACACTTTGGGAGGCCAAGGCGGGCAGCTAACCTGAGGTCAGAAGTTCGAGATT A G GTPBP4 Ensembl:ENSG00000107937 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1008311937 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_141554,RMVar_hsa_circ_141555,RMVar_hsa_circ_141553 38288 RMVar_ID_38288 Human_SNP_ID_419028984 A-to-I Human chr10 + 999772 999772 999772 CCTGAGGTCAGAAGTTCGAGATTGGCCTGGCCAACATGGCGAAACCCCATCTCTACTAAAAATAC CCTGAGGTCAGAAGTTCGAGATTGGCCTGGCCGACATGGCGAAACCCCATCTCTACTAAAAATAC A G GTPBP4 Ensembl:ENSG00000107937 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1211833967 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_141554,RMVar_hsa_circ_141555,RMVar_hsa_circ_141553 38289 RMVar_ID_38289 Human_SNP_ID_419029005 A-to-I Human chr10 + 999848 999848 999848 GGACGTGGTGGTGGGTGCCTGTAATCCCAGCTACTTGGAAGGCTGAGGCTGGAGAATCGCTTGAA GGACGTGGTGGTGGGTGCCTGTAATCCCAGCTGCTTGGAAGGCTGAGGCTGGAGAATCGCTTGAA A G GTPBP4 Ensembl:ENSG00000107937 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1269392735 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_141554,RMVar_hsa_circ_141555,RMVar_hsa_circ_141553 38290 RMVar_ID_38290 Human_SNP_ID_419029179 A-to-I Human chr10 + 1000377 1000377 1000377 CTCCTACCTCAGCCTCCCGAGTAGCTGGGACTACAGGTGCCCGCCACCACGCCCAGCTAATTTTT CTCCTACCTCAGCCTCCCGAGTAGCTGGGACTGCAGGTGCCCGCCACCACGCCCAGCTAATTTTT A G GTPBP4 Ensembl:ENSG00000107937 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs760623612 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_141554,RMVar_hsa_circ_141555,RMVar_hsa_circ_141553 38291 RMVar_ID_38291 Human_SNP_ID_419037458 A-to-I Human chr10 + 1026174 1026174 1026174 CTCTGTTGCCCAGGCCAGAGTGCAGTGGCGTGATCTCGGCTGACTGCAACCTCTGCCTCCCGGGT CTCTGTTGCCCAGGCCAGAGTGCAGTGGCGTGGTCTCGGCTGACTGCAACCTCTGCCTCCCGGGT A G IDI2-AS1 Ensembl:ENSG00000232656 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1257838566 Functional Loss SNV dbSNP153 33..33 33 - - - 38292 RMVar_ID_38292 Human_SNP_ID_419172342 A-to-I Human chr10 - 1498151 1498151 1498151 CAGGTTGGTCTTCGAACTCCTGACCCCAGGTGATCCACCTGCCTCAGCCTCCCAAAGTGCCGGGA CAGGTTGGTCTTCGAACTCCTGACCCCAGGTGGTCCACCTGCCTCAGCCTCCCAAAGTGCCGGGA T C ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1422798200 Functional Loss SNV dbSNP153 33..33 33 - - - 38293 RMVar_ID_38293 Human_SNP_ID_419176066 A-to-I Human chr10 - 1510273 1510273 1510273 ATGAAGCTGAGACAGGAGAATCACTTAAGCCCAGGAGCTCAAGGCTGCAGTGAGCCGAGATTGTG ATGAAGCTGAGACAGGAGAATCACTTAAGCCCGGGAGCTCAAGGCTGCAGTGAGCCGAGATTGTG T C ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1246337135 Functional Loss SNV dbSNP153 33..33 33 - - - 38294 RMVar_ID_38294 Human_SNP_ID_419176103 A-to-I Human chr10 - 1510409 1510409 1510409 GGGATGCTGAGGAGGGAGGATTGCTTGAGCTCAGGAGTTCGAGACAAGCCTGGGCAACATAGTGA GGGATGCTGAGGAGGGAGGATTGCTTGAGCTCCGGAGTTCGAGACAAGCCTGGGCAACATAGTGA T G ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1163190961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2202660 38295 RMVar_ID_38295 Human_SNP_ID_419176226 A-to-I Human chr10 - 1510955 1510955 1510955 CCAGCTACTCAGGAGGCTGAGGTGGTAGGATCACTCGAGCCAGAAGGTTGAGGCTGCAGTGAGCC CCAGCTACTCAGGAGGCTGAGGTGGTAGGATCTCTCGAGCCAGAAGGTTGAGGCTGCAGTGAGCC T A ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1306931959 Functional Loss SNV dbSNP153 33..33 33 - - - 38296 RMVar_ID_38296 Human_SNP_ID_419176234 A-to-I Human chr10 - 1510993 1510993 1510993 AAAAAATTAGCCGGACATGGTAGCATGCACCTATAGTCCCAGCTACTCAGGAGGCTGAGGTGGTA AAAAAATTAGCCGGACATGGTAGCATGCACCTGTAGTCCCAGCTACTCAGGAGGCTGAGGTGGTA T C ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1454138856 Functional Loss SNV dbSNP153 33..33 33 - - - 38297 RMVar_ID_38297 Human_SNP_ID_419182251 A-to-I Human chr10 - 1531721 1531721 1531721 GTGATTCTCCTGCCTCAGCCTCCCGAGTAGCTAGGATTACAGGCATTTGACACCACATCCAGCTA GTGATTCTCCTGCCTCAGCCTCCCGAGTAGCTTGGATTACAGGCATTTGACACCACATCCAGCTA T A ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1004118695 Functional Loss SNV dbSNP153 33..33 33 - - - 38298 RMVar_ID_38298 Human_SNP_ID_419182252 A-to-I Human chr10 - 1531721 1531721 1531721 GTGATTCTCCTGCCTCAGCCTCCCGAGTAGCTAGGATTACAGGCATTTGACACCACATCCAGCTA GTGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCATTTGACACCACATCCAGCTA T C ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1004118695 Functional Loss SNV dbSNP153 33..33 33 - - - 38299 RMVar_ID_38299 Human_SNP_ID_419182253 A-to-I Human chr10 - 1531721 1531721 1531721 GTGATTCTCCTGCCTCAGCCTCCCGAGTAGCTAGGATTACAGGCATTTGACACCACATCCAGCTA GTGATTCTCCTGCCTCAGCCTCCCGAGTAGCTCGGATTACAGGCATTTGACACCACATCCAGCTA T G ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1004118695 Functional Loss SNV dbSNP153 33..33 33 - - - 38300 RMVar_ID_38300 Human_SNP_ID_419182267 A-to-I Human chr10 - 1531785 1531785 1531785 TCACCCAGGCTGGAGTGCAGTGGCACAATCTCAGCTTACTGCAACCTCCGCCTCCGGGGTTCAAG TCACCCAGGCTGGAGTGCAGTGGCACAATCTCGGCTTACTGCAACCTCCGCCTCCGGGGTTCAAG T C ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1412230712 Functional Loss SNV dbSNP153 33..33 33 - - - 38301 RMVar_ID_38301 Human_SNP_ID_419183271 A-to-I Human chr10 - 1535032 1535032 1535032 TTGCCTCGTCCTAGCTCATTCACCTGTGAATAACTCACCCCGTCCCTGGTGGCTCGCACCTCTGC TTGCCTCGTCCTAGCTCATTCACCTGTGAATATCTCACCCCGTCCCTGGTGGCTCGCACCTCTGC T A ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs970858122 Functional Loss SNV dbSNP153 33..33 33 - - - 38302 RMVar_ID_38302 Human_SNP_ID_419183526 A-to-I Human chr10 - 1535847 1535847 1535847 CTGGCCCCCACGCCTCAGCAGAACAACTCTGAACTTCTATGGACTCACAGGGGCGAGGTCGGGGC CTGGCCCCCACGCCTCAGCAGAACAACTCTGAGCTTCTATGGACTCACAGGGGCGAGGTCGGGGC T C ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs781690358 Functional Loss SNV dbSNP153 33..33 33 - - - 38303 RMVar_ID_38303 Human_SNP_ID_419183548 A-to-I Human chr10 - 1535929 1535929 1535929 TGATGTCTGCCTCCCTTTCAAATGAAAGGAAAAGACTGGGACGAGAGAGGGCGGCACTCCCCAGA TGATGTCTGCCTCCCTTTCAAATGAAAGGAAAGGACTGGGACGAGAGAGGGCGGCACTCCCCAGA T C ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1413292266 Functional Loss SNV dbSNP153 33..33 33 - - - 38304 RMVar_ID_38304 Human_SNP_ID_419203148 A-to-I Human chr10 - 1600620 1600620 1600620 TCTCACTCTGTTGCCCAGGCTGGGGTGCAGTGATGCAATTTCGGCTCATTGCAGCCTCCGCCTCC TCTCACTCTGTTGCCCAGGCTGGGGTGCAGTGTTGCAATTTCGGCTCATTGCAGCCTCCGCCTCC T A ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs554043639 Functional Loss SNV dbSNP153 33..33 33 - - - 38305 RMVar_ID_38305 Human_SNP_ID_419208904 A-to-I Human chr10 - 1619590 1619590 1619590 AAAATTAGCTGGGCATGGTGGCATACCCCTGTAATCCCAGCTACTTGGGAGGCTGAGACAGGAGA AAAATTAGCTGGGCATGGTGGCATACCCCTGTCATCCCAGCTACTTGGGAGGCTGAGACAGGAGA T G ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1460735406 Functional Loss SNV dbSNP153 33..33 33 - - - 38306 RMVar_ID_38306 Human_SNP_ID_419209924 A-to-I Human chr10 - 1623982 1623982 1623982 GTGATCGATCCGCCTCAGCCTCCCAAATCGCTAGATCATACGTGTGAGTCACTGCACCAGCCTTG GTGATCGATCCGCCTCAGCCTCCCAAATCGCTGGATCATACGTGTGAGTCACTGCACCAGCCTTG T C ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878890372 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2204944,Human_RBP_ID_8986216 38307 RMVar_ID_38307 Human_SNP_ID_419636113 A-to-I Human chr10 + 3093737 3093737 3093737 GCAATCTCAGCTCACTGCAAGCTCCGCCTCCCAGGTTCACGCCATTCTCCCGCCTCAGCCTCCCG GCAATCTCAGCTCACTGCAAGCTCCGCCTCCCGGGTTCACGCCATTCTCCCGCCTCAGCCTCCCG A G PFKP Ensembl:ENSG00000067057 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs538661395 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_141627,RMVar_hsa_circ_313987,RMVar_hsa_circ_141626,RMVar_hsa_circ_335809,RMVar_hsa_circ_141628 38308 RMVar_ID_38308 Human_SNP_ID_419639698 A-to-I Human chr10 + 3102334 3102334 3102334 TTAGACGATAAATCTCTGCCAATACATCATCCAGTACCAACTTTGGCACTACTTAGGAAAGCGTT TTAGACGATAAATCTCTGCCAATACATCATCCGGTACCAACTTTGGCACTACTTAGGAAAGCGTT A G PFKP Ensembl:ENSG00000067057 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11251718 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_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 38309 RMVar_ID_38309 Human_SNP_ID_419649569 A-to-I Human chr10 + 3126683 3126683 3126683 TCACAGAGCAAGGTGGTTCTCACAGAGAAGTCAGTGGCTTTTTTCTACGTTAATGCTGTAGCAAA TCACAGAGCAAGGTGGTTCTCACAGAGAAGTCGGTGGCTTTTTTCTACGTTAATGCTGTAGCAAA A G PFKP Ensembl:ENSG00000067057 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs532251241 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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 38310 RMVar_ID_38310 Human_SNP_ID_419650205 A-to-I Human chr10 - 3128369 3128368 3128369 AGGAAAACACCACCTGGTTTCTAGGACCACAAAGTTCCCTCTGTCAGGGGCTCTCGGAGCCACCC AGGAAAACACCACCTGGTTTCTAGGACCACAA_GTTCCCTCTGTCAGGGGCTCTCGGAGCCACCC CT C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs776723173 Functional Loss DEL dbSNP153 33..33 33 - - - 38311 RMVar_ID_38311 Human_SNP_ID_419659103 A-to-I Human chr10 - 3150534 3150534 3150534 ACTGAGCTGAGGGCAGCATGGCTCTCACTTGCACCTTGAGGACGGGGATGGGATTTCACCCTGGG ACTGAGCTGAGGGCAGCATGGCTCTCACTTGCGCCTTGAGGACGGGGATGGGATTTCACCCTGGG T C PITRM1 Ensembl:ENSG00000107959 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs570409990 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_46752,RMVar_hsa_circ_115244,RMVar_hsa_circ_141661,RMVar_hsa_circ_22817,RMVar_hsa_circ_88439,RMVar_hsa_circ_336747,RMVar_hsa_circ_141662,RMVar_hsa_circ_141663,RMVar_hsa_circ_103997,RMVar_hsa_circ_141665,RMVar_hsa_circ_3649,RMVar_hsa_circ_316399,RMVar_hsa_circ_123071,RMVar_hsa_circ_5397,RMVar_hsa_circ_141667,RMVar_hsa_circ_370439,RMVar_hsa_circ_49958,RMVar_hsa_circ_69747,RMVar_hsa_circ_38569,RMVar_hsa_circ_141668 38312 RMVar_ID_38312 Human_SNP_ID_419826790 A-to-I Human chr10 - 3781037 3781032 3781037 CCTAGGTGAAAGTGCTATTTAAAAATACCTTGACATGTTCTAGGATAATTGGTGAGGAATCACAG CCTAGGTGAAAGTGCTATTTAAAAATACCTTG_____TTCTAGGATAATTGGTGAGGAATCACAG ACATGT A KLF6 Ensembl:ENSG00000067082 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1360278042 Functional Loss DEL dbSNP153 33..37 33 - - - RMVar_hsa_circ_81579,RMVar_hsa_circ_121885,RMVar_hsa_circ_91517,RMVar_hsa_circ_141682,RMVar_hsa_circ_141683,RMVar_hsa_circ_141684 38313 RMVar_ID_38313 Human_SNP_ID_419826793 A-to-I Human chr10 - 3781037 3781037 3781037 CCTAGGTGAAAGTGCTATTTAAAAATACCTTGACATGTTCTAGGATAATTGGTGAGGAATCACAG CCTAGGTGAAAGTGCTATTTAAAAATACCTTGGCATGTTCTAGGATAATTGGTGAGGAATCACAG T C KLF6 Ensembl:ENSG00000067082 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1228290124 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81579,RMVar_hsa_circ_121885,RMVar_hsa_circ_91517,RMVar_hsa_circ_141682,RMVar_hsa_circ_141683,RMVar_hsa_circ_141684 38314 RMVar_ID_38314 Human_SNP_ID_420159411 A-to-I Human chr10 + 4972261 4972261 4972261 GAAAACTGCTGGATTTCTGCAAGTCAAAAGACATTGTTCTGGTTGCCTATAGTGCTCTGGGATCC GAAAACTGCTGGATTTCTGCAAGTCAAAAGACGTTGTTCTGGTTGCCTATAGTGCTCTGGGATCC A G AKR1C1 Ensembl:ENSG00000187134 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs369381901 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22752546 Human_Splice_Rec_1108100,Human_Splice_Rec_1108101,Human_Splice_Rec_1108116,Human_Splice_Rec_1108117,Human_Splice_Rec_1108132,Human_Splice_Rec_1108133 Human_miRNA_ID_2944339 RMVar_hsa_circ_61362,RMVar_hsa_circ_89943,RMVar_hsa_circ_141709,RMVar_hsa_circ_104054,RMVar_hsa_circ_141710,RMVar_hsa_circ_85969,RMVar_hsa_circ_104644,RMVar_hsa_circ_97531,RMVar_hsa_circ_114231,RMVar_hsa_circ_141712,RMVar_hsa_circ_141713,RMVar_hsa_circ_141715,RMVar_hsa_circ_82434,RMVar_hsa_circ_141714,RMVar_hsa_circ_371934,RMVar_hsa_circ_141716,RMVar_hsa_circ_141717 38315 RMVar_ID_38315 Human_SNP_ID_420159412 A-to-I Human chr10 + 4972261 4972261 4972261 GAAAACTGCTGGATTTCTGCAAGTCAAAAGACATTGTTCTGGTTGCCTATAGTGCTCTGGGATCC GAAAACTGCTGGATTTCTGCAAGTCAAAAGACTTTGTTCTGGTTGCCTATAGTGCTCTGGGATCC A T AKR1C1 Ensembl:ENSG00000187134 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs369381901 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22752546 Human_Splice_Rec_1108100,Human_Splice_Rec_1108101,Human_Splice_Rec_1108116,Human_Splice_Rec_1108117,Human_Splice_Rec_1108132,Human_Splice_Rec_1108133 Human_miRNA_ID_2944339 RMVar_hsa_circ_61362,RMVar_hsa_circ_89943,RMVar_hsa_circ_141709,RMVar_hsa_circ_104054,RMVar_hsa_circ_141710,RMVar_hsa_circ_85969,RMVar_hsa_circ_104644,RMVar_hsa_circ_97531,RMVar_hsa_circ_114231,RMVar_hsa_circ_141712,RMVar_hsa_circ_141713,RMVar_hsa_circ_141715,RMVar_hsa_circ_82434,RMVar_hsa_circ_141714,RMVar_hsa_circ_371934,RMVar_hsa_circ_141716,RMVar_hsa_circ_141717 38316 RMVar_ID_38316 Human_SNP_ID_420159420 A-to-I Human chr10 + 4972279 4972279 4972279 GCAAGTCAAAAGACATTGTTCTGGTTGCCTATAGTGCTCTGGGATCCCACCGAGAAGAACCATGG GCAAGTCAAAAGACATTGTTCTGGTTGCCTATGGTGCTCTGGGATCCCACCGAGAAGAACCATGG A G AKR1C1 Ensembl:ENSG00000187134 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs782504158 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_747867,Human_RBP_ID_805314,Human_RBP_ID_863845,Human_RBP_ID_22431364,Human_RBP_ID_22752546 Human_Splice_Rec_1108100,Human_Splice_Rec_1108101,Human_Splice_Rec_1108116,Human_Splice_Rec_1108117,Human_Splice_Rec_1108132,Human_Splice_Rec_1108133 Human_miRNA_ID_2944339 RMVar_hsa_circ_61362,RMVar_hsa_circ_89943,RMVar_hsa_circ_141709,RMVar_hsa_circ_104054,RMVar_hsa_circ_141710,RMVar_hsa_circ_85969,RMVar_hsa_circ_104644,RMVar_hsa_circ_97531,RMVar_hsa_circ_114231,RMVar_hsa_circ_141712,RMVar_hsa_circ_141713,RMVar_hsa_circ_141715,RMVar_hsa_circ_82434,RMVar_hsa_circ_141714,RMVar_hsa_circ_371934,RMVar_hsa_circ_141716,RMVar_hsa_circ_141717 38317 RMVar_ID_38317 Human_SNP_ID_420160118 A-to-I Human chr10 + 4974345 4974345 4974345 ATTTATTCTGGATATTAATTCTTTAGAGACTTAAATGTATTCTTGAAATAACATCTCCCAAATTT ATTTATTCTGGATATTAATTCTTTAGAGACTTGAATGTATTCTTGAAATAACATCTCCCAAATTT A G AKR1C1 Ensembl:ENSG00000187134 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1227612042 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17558874 RMVar_hsa_circ_61362,RMVar_hsa_circ_89943,RMVar_hsa_circ_141709,RMVar_hsa_circ_104054,RMVar_hsa_circ_141710,RMVar_hsa_circ_85969,RMVar_hsa_circ_104644,RMVar_hsa_circ_97531,RMVar_hsa_circ_114231,RMVar_hsa_circ_141712,RMVar_hsa_circ_141713,RMVar_hsa_circ_141715,RMVar_hsa_circ_82434,RMVar_hsa_circ_141714,RMVar_hsa_circ_141717 38318 RMVar_ID_38318 Human_SNP_ID_420161589 A-to-I Human chr10 + 4979676 4979676 4979676 TAGGTCAGTCATTTGTAAATAGTACATCTGCTATGGACTTTTTCCAGTTCTTCACCATCCATTTT TAGGTCAGTCATTTGTAAATAGTACATCTGCTGTGGACTTTTTCCAGTTCTTCACCATCCATTTT A G AKR1C1 Ensembl:ENSG00000187134 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs797042714 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21881965 RMVar_hsa_circ_89943,RMVar_hsa_circ_141710 38319 RMVar_ID_38319 Human_SNP_ID_420161969 A-to-I Human chr10 + 4981243 4981243 4981243 CTTTATTTATAGAACACTTACAGAGTAGATATAGATTAAATCTTAAGGACCCTAGGATTGTTAGA CTTTATTTATAGAACACTTACAGAGTAGATATCGATTAAATCTTAAGGACCCTAGGATTGTTAGA A C AKR1C1 Ensembl:ENSG00000187134 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1308442694 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89943,RMVar_hsa_circ_141710 38320 RMVar_ID_38320 Human_SNP_ID_420161971 A-to-I Human chr10 + 4981264 4981264 4981264 AGAGTAGATATAGATTAAATCTTAAGGACCCTAGGATTGTTAGAATAGTAAATGAACATCATATG AGAGTAGATATAGATTAAATCTTAAGGACCCTTGGATTGTTAGAATAGTAAATGAACATCATATG A T AKR1C1 Ensembl:ENSG00000187134 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1372066558 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89943,RMVar_hsa_circ_141710 38321 RMVar_ID_38321 Human_SNP_ID_420162526 A-to-I Human chr10 + 4982903 4982903 4982903 GCGTACCACACCCTGACCAGTCAGAGGTCTTGAGTCGGTCCGCATGACAAGTTCACCGCTCGCAT GCGTACCACACCCTGACCAGTCAGAGGTCTTGGGTCGGTCCGCATGACAAGTTCACCGCTCGCAT A G AKR1C1 Ensembl:ENSG00000187134 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1564321607 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22708522 RMVar_hsa_circ_89943,RMVar_hsa_circ_141710 38322 RMVar_ID_38322 Human_SNP_ID_420162540 A-to-I Human chr10 + 4982936 4982936 4982936 GTCGGTCCGCATGACAAGTTCACCGCTCGCATAACCAGCATTCAAGAAAGCCAGCACACTAAGCC GTCGGTCCGCATGACAAGTTCACCGCTCGCATGACCAGCATTCAAGAAAGCCAGCACACTAAGCC A G AKR1C1 Ensembl:ENSG00000187134 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1396079617 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89943,RMVar_hsa_circ_141710 38323 RMVar_ID_38323 Human_SNP_ID_420163597 A-to-I Human chr10 + 4986825 4986825 4986825 GGAAATACATTTCATAAATATATGGCTACCATAGTGATTGGTCTGAAGAATCTGTGAAAAGAAAA GGAAATACATTTCATAAATATATGGCTACCATGGTGATTGGTCTGAAGAATCTGTGAAAAGAAAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1554771570 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89943,RMVar_hsa_circ_141710 38324 RMVar_ID_38324 Human_SNP_ID_420164882 A-to-I Human chr10 + 4991538 4991538 4991538 ATATCCACAGTGTGTACACTAGACAGTAATACAAACGGCAGGCCTACATGGAAGGTGCAGATTCA ATATCCACAGTGTGTACACTAGACAGTAATACTAACGGCAGGCCTACATGGAAGGTGCAGATTCA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1464703080 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89943,RMVar_hsa_circ_141710 38325 RMVar_ID_38325 Human_SNP_ID_420165571 A-to-I Human chr10 - 4994211 4994211 4994211 AATTCATACAAGTCTCTAAAGAATTAACATCCAGAATACATACATATGTGTATGTTTTCTAATTA AATTCATACAAGTCTCTAAAGAATTAACATCCGGAATACATACATATGTGTATGTTTTCTAATTA T C AKR1C2 Ensembl:ENSG00000151632 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1481529349 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69713,RMVar_hsa_circ_362486,RMVar_hsa_circ_65022 38326 RMVar_ID_38326 Human_SNP_ID_420169104 A-to-I Human chr10 - 5006481 5006481 5006481 TTCCTGGCTTAGCCTCCGGAGTAGCTGGAATTACAGATGTGCGCCCCCATGACCAGCTAATTTTT TTCCTGGCTTAGCCTCCGGAGTAGCTGGAATTGCAGATGTGCGCCCCCATGACCAGCTAATTTTT T C AKR1C2 Ensembl:ENSG00000151632 Protein coding intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1224366475 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43370,RMVar_hsa_circ_65022,RMVar_hsa_circ_358051 38327 RMVar_ID_38327 Human_SNP_ID_420169120 A-to-I Human chr10 - 5006550 5006550 5006550 AGCCCAAGCTGGAGTGCGATGGTGCAATCCCAACTCACTGCAACCTCTGCCTCCCAGGTTCAAGC AGCCCAAGCTGGAGTGCGATGGTGCAATCCCAGCTCACTGCAACCTCTGCCTCCCAGGTTCAAGC T C AKR1C2 Ensembl:ENSG00000151632 Protein coding intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1170476116 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1108226 RMVar_hsa_circ_43370,RMVar_hsa_circ_65022,RMVar_hsa_circ_358051 38328 RMVar_ID_38328 Human_SNP_ID_420366413 A-to-I Human chr10 + 5708795 5708795 5708795 GCAATCTCAGCTCACTGCAACTTCTTCCCCCCAGACTCAAGCCATCGTCCCACCTCAGCCTCCAA GCAATCTCAGCTCACTGCAACTTCTTCCCCCCGGACTCAAGCCATCGTCCCACCTCAGCCTCCAA A G TASOR2 Ensembl:ENSG00000108021 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1440965724 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93748,RMVar_hsa_circ_103410,RMVar_hsa_circ_141739,RMVar_hsa_circ_141740,RMVar_hsa_circ_141741 38329 RMVar_ID_38329 Human_SNP_ID_420368020 A-to-I Human chr10 + 5715772 5715772 5715772 TCAAGTGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGAGATTACAGGCACACATCACCATGCATA TCAAGTGATTCTCCTGCCTCAGCCTCCTGAGTGGCTGAGATTACAGGCACACATCACCATGCATA A G TASOR2 Ensembl:ENSG00000108021 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1465263860 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93748,RMVar_hsa_circ_141742,RMVar_hsa_circ_141739,RMVar_hsa_circ_141744,RMVar_hsa_circ_141745,RMVar_hsa_circ_141743,RMVar_hsa_circ_26688,RMVar_hsa_circ_141750,RMVar_hsa_circ_347871,RMVar_hsa_circ_367579,RMVar_hsa_circ_72515,RMVar_hsa_circ_30246,RMVar_hsa_circ_338248 38330 RMVar_ID_38330 Human_SNP_ID_420369934 A-to-I Human chr10 + 5723240 5723240 5723240 ACCACATCCGGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCGAGTTAGCCAGGATGG ACCACATCCGGCTAATTTTTTGTATTTTTAGTGGAGACGGGGTTTCACCGAGTTAGCCAGGATGG A G TASOR2 Ensembl:ENSG00000108021 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1203854724 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1150,RMVar_hsa_circ_93748,RMVar_hsa_circ_141742,RMVar_hsa_circ_141739,RMVar_hsa_circ_141744,RMVar_hsa_circ_141743,RMVar_hsa_circ_141750,RMVar_hsa_circ_347871,RMVar_hsa_circ_72515,RMVar_hsa_circ_104317,RMVar_hsa_circ_338248,RMVar_hsa_circ_349601,RMVar_hsa_circ_370345,RMVar_hsa_circ_334878,RMVar_hsa_circ_105337,RMVar_hsa_circ_92584,RMVar_hsa_circ_72308,RMVar_hsa_circ_57334,RMVar_hsa_circ_141752,RMVar_hsa_circ_141754,RMVar_hsa_circ_141755,RMVar_hsa_circ_141753,RMVar_hsa_circ_141751,RMVar_hsa_circ_316074,RMVar_hsa_circ_7481,RMVar_hsa_circ_283530,RMVar_hsa_circ_356289,RMVar_hsa_circ_141757,RMVar_hsa_circ_376826,RMVar_hsa_circ_291169,RMVar_hsa_circ_276259,RMVar_hsa_circ_88098,RMVar_hsa_circ_141758,RMVar_hsa_circ_141759,RMVar_hsa_circ_124218,RMVar_hsa_circ_141760,RMVar_hsa_circ_141761 38331 RMVar_ID_38331 Human_SNP_ID_420372182 A-to-I Human chr10 + 5731453 5731453 5731453 GGAAGGTTGAGGCACAAGAATCATTTGAACCCAAGAGACAGAGGTTGCAGTGAGCCGAGATCACG GGAAGGTTGAGGCACAAGAATCATTTGAACCCCAGAGACAGAGGTTGCAGTGAGCCGAGATCACG A C TASOR2 Ensembl:ENSG00000108021 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1036318027 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93748,RMVar_hsa_circ_141739,RMVar_hsa_circ_338248,RMVar_hsa_circ_349601,RMVar_hsa_circ_370345,RMVar_hsa_circ_105337,RMVar_hsa_circ_92584,RMVar_hsa_circ_72308,RMVar_hsa_circ_80958,RMVar_hsa_circ_141752,RMVar_hsa_circ_141753,RMVar_hsa_circ_141751,RMVar_hsa_circ_7481,RMVar_hsa_circ_356289,RMVar_hsa_circ_376826,RMVar_hsa_circ_124218,RMVar_hsa_circ_141761,RMVar_hsa_circ_50210,RMVar_hsa_circ_111415,RMVar_hsa_circ_56715,RMVar_hsa_circ_141763,RMVar_hsa_circ_298497,RMVar_hsa_circ_141764,RMVar_hsa_circ_354798,RMVar_hsa_circ_62192,RMVar_hsa_circ_141767,RMVar_hsa_circ_367304,RMVar_hsa_circ_290237 38332 RMVar_ID_38332 Human_SNP_ID_420377890 A-to-I Human chr10 + 5752512 5752512 5752512 TGCCCACTGGGTCTGTCTCAGACTTCACTTACATCACTTCTGCTGATTTCCTGCGCTAACTCCAG TGCCCACTGGGTCTGTCTCAGACTTCACTTACGTCACTTCTGCTGATTTCCTGCGCTAACTCCAG A G TASOR2 Ensembl:ENSG00000108021 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2669138 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_4335,GWAS_ID_4336,GWAS_ID_4337,GWAS_ID_4338,GWAS_ID_4339,GWAS_ID_4340,GWAS_ID_4341 RMVar_hsa_circ_105337,RMVar_hsa_circ_92584,RMVar_hsa_circ_34796,RMVar_hsa_circ_141752,RMVar_hsa_circ_141751,RMVar_hsa_circ_7481,RMVar_hsa_circ_50210,RMVar_hsa_circ_111415,RMVar_hsa_circ_141764,RMVar_hsa_circ_69481,RMVar_hsa_circ_62192,RMVar_hsa_circ_69725,RMVar_hsa_circ_121611,RMVar_hsa_circ_141769 38333 RMVar_ID_38333 Human_SNP_ID_420385834 A-to-I Human chr10 - 5780087 5780087 5780087 TTCCCATCTCAGCCTCTTGAGTAGTAGGGACTACAGGCATGCACCACCCCACCTGGCTAACTTTT TTCCCATCTCAGCCTCTTGAGTAGTAGGGACTGCAGGCATGCACCACCCCACCTGGCTAACTTTT T C GDI2 Ensembl:ENSG00000057608 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1303357025 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11376754,Human_RBP_ID_24816932 RMVar_hsa_circ_141774,RMVar_hsa_circ_115518,RMVar_hsa_circ_126821,RMVar_hsa_circ_119308,RMVar_hsa_circ_106043,RMVar_hsa_circ_96921,RMVar_hsa_circ_141776,RMVar_hsa_circ_141775,RMVar_hsa_circ_141784,RMVar_hsa_circ_141772,RMVar_hsa_circ_141773,RMVar_hsa_circ_357087,RMVar_hsa_circ_141779,RMVar_hsa_circ_266675,RMVar_hsa_circ_141782,RMVar_hsa_circ_141781,RMVar_hsa_circ_281208,RMVar_hsa_circ_271927,RMVar_hsa_circ_375650,RMVar_hsa_circ_265540,RMVar_hsa_circ_48483,RMVar_hsa_circ_79431,RMVar_hsa_circ_141785,RMVar_hsa_circ_141786,RMVar_hsa_circ_141788,RMVar_hsa_circ_298665,RMVar_hsa_circ_277849,RMVar_hsa_circ_141787 38334 RMVar_ID_38334 Human_SNP_ID_420388419 A-to-I Human chr10 - 5788970 5788970 5788970 TTGAGGTCAGGAGTTTGACACCAGCCTGTCCAACATGGTGAAACCCCATCTCTACTAAAAATACA TTGAGGTCAGGAGTTTGACACCAGCCTGTCCAGCATGGTGAAACCCCATCTCTACTAAAAATACA T C GDI2 Ensembl:ENSG00000057608 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1179781549 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_141774,RMVar_hsa_circ_115518,RMVar_hsa_circ_119308,RMVar_hsa_circ_106043,RMVar_hsa_circ_141784,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_375650,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_296580,RMVar_hsa_circ_141790,RMVar_hsa_circ_17637,RMVar_hsa_circ_141789,RMVar_hsa_circ_337432,RMVar_hsa_circ_141793,RMVar_hsa_circ_288869,RMVar_hsa_circ_141792 38335 RMVar_ID_38335 Human_SNP_ID_420388844 A-to-I Human chr10 - 5790607 5790607 5790607 AGCTTTGCTCTTGTTGCCCAGGCTGGAGTTCAATGGTGTAATCTTGGCTCACTGCAACTTCCACC AGCTTTGCTCTTGTTGCCCAGGCTGGAGTTCAGTGGTGTAATCTTGGCTCACTGCAACTTCCACC T C GDI2 Ensembl:ENSG00000057608 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs548416150 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_141774,RMVar_hsa_circ_115518,RMVar_hsa_circ_119308,RMVar_hsa_circ_106043,RMVar_hsa_circ_141784,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_375650,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_296580,RMVar_hsa_circ_141790,RMVar_hsa_circ_17637,RMVar_hsa_circ_141789,RMVar_hsa_circ_337432,RMVar_hsa_circ_141793,RMVar_hsa_circ_288869,RMVar_hsa_circ_141792 38336 RMVar_ID_38336 Human_SNP_ID_420389621 A-to-I Human chr10 - 5793194 5793194 5793194 GGCCAGGAGTTGAAGACCAGCCTGGGCAACATAGCAGGACCCTGTCTCTTCAAAAAATAAGAAAA GGCCAGGAGTTGAAGACCAGCCTGGGCAACATGGCAGGACCCTGTCTCTTCAAAAAATAAGAAAA T C GDI2 Ensembl:ENSG00000057608 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs575592083 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11377018 RMVar_hsa_circ_141774,RMVar_hsa_circ_115518,RMVar_hsa_circ_119308,RMVar_hsa_circ_106043,RMVar_hsa_circ_141784,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_375650,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_296580,RMVar_hsa_circ_141790,RMVar_hsa_circ_17637,RMVar_hsa_circ_141789,RMVar_hsa_circ_337432,RMVar_hsa_circ_141793,RMVar_hsa_circ_288869,RMVar_hsa_circ_141792 38337 RMVar_ID_38337 Human_SNP_ID_420392103 A-to-I Human chr10 - 5801589 5801589 5801589 TCACCACAACCTCTGCCTCCCAGGTTCAAGCAATTCACCTGCCTTGGCCTCTTGAATAGCTAGGA TCACCACAACCTCTGCCTCCCAGGTTCAAGCAGTTCACCTGCCTTGGCCTCTTGAATAGCTAGGA T C GDI2 Ensembl:ENSG00000057608 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs973055379 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115518,RMVar_hsa_circ_141772,RMVar_hsa_circ_79431,RMVar_hsa_circ_141786,RMVar_hsa_circ_124483,RMVar_hsa_circ_268769,RMVar_hsa_circ_141789,RMVar_hsa_circ_362230 38338 RMVar_ID_38338 Human_SNP_ID_420392123 A-to-I Human chr10 - 5801664 5801657 5801665 ACATCCTTTTTTTTGTTCTTGAGATGGAGTTTAGCTCTTGTTGCCCAGGCTGGAGTGCAGTGGTG ACATCCTTTTTTTTGTTCTTGAGATGGAGTT________GTTGCCCAGGCTGGAGTGCAGTGGTG CAAGAGCTA C GDI2 Ensembl:ENSG00000057608 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1230180958 Functional Loss DEL dbSNP153 32..39 33 - - - Human_RBP_ID_11484958 RMVar_hsa_circ_115518,RMVar_hsa_circ_141772,RMVar_hsa_circ_79431,RMVar_hsa_circ_141786,RMVar_hsa_circ_124483,RMVar_hsa_circ_268769,RMVar_hsa_circ_141789,RMVar_hsa_circ_362230 38339 RMVar_ID_38339 Human_SNP_ID_420392207 A-to-I Human chr10 - 5801956 5801956 5801956 TCACCCAGGCTGGAGTGCAGTGGCGTGGTCTCAGCTCACAGCAGCCTCTGCCTCCTGGGTTCAAG TCACCCAGGCTGGAGTGCAGTGGCGTGGTCTCGGCTCACAGCAGCCTCTGCCTCCTGGGTTCAAG T C GDI2 Ensembl:ENSG00000057608 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1439684933 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2272616,Human_miRNA_ID_2672602,Human_miRNA_ID_2714378,Human_miRNA_ID_3050357 RMVar_hsa_circ_115518,RMVar_hsa_circ_141772,RMVar_hsa_circ_79431,RMVar_hsa_circ_141786,RMVar_hsa_circ_124483,RMVar_hsa_circ_268769,RMVar_hsa_circ_141789,RMVar_hsa_circ_362230 38340 RMVar_ID_38340 Human_SNP_ID_420392588 A-to-I Human chr10 - 5803300 5803300 5803300 CCCACCTCTCAGCCTCTTGAGTAGCAGGGACTACAGGTGCTCACCACCACACCCAGCTAATTTTT CCCACCTCTCAGCCTCTTGAGTAGCAGGGACTGCAGGTGCTCACCACCACACCCAGCTAATTTTT T C GDI2 Ensembl:ENSG00000057608 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs780536905 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115518,RMVar_hsa_circ_141772,RMVar_hsa_circ_79431,RMVar_hsa_circ_141786,RMVar_hsa_circ_124483,RMVar_hsa_circ_268769,RMVar_hsa_circ_141789,RMVar_hsa_circ_362230 38341 RMVar_ID_38341 Human_SNP_ID_420392856 A-to-I Human chr10 - 5804161 5804161 5804161 TGAACCTGGGAGGTGAAGGTTGCATTGAGCCAAGATCGCGCCACTGCACTCCAGTCTGGGCAACA TGAACCTGGGAGGTGAAGGTTGCATTGAGCCAGGATCGCGCCACTGCACTCCAGTCTGGGCAACA T C GDI2 Ensembl:ENSG00000057608 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs990600339 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11377361 RMVar_hsa_circ_115518,RMVar_hsa_circ_141772,RMVar_hsa_circ_79431,RMVar_hsa_circ_141786,RMVar_hsa_circ_124483,RMVar_hsa_circ_268769,RMVar_hsa_circ_141789,RMVar_hsa_circ_362230 38342 RMVar_ID_38342 Human_SNP_ID_420393103 A-to-I Human chr10 - 5805037 5805037 5805037 ATGAGGTCAGGAGTTTGAGACCAGCCTGTCCAAGATGGTGAAACCCCATCTGTACTAAAAATACA ATGAGGTCAGGAGTTTGAGACCAGCCTGTCCAGGATGGTGAAACCCCATCTGTACTAAAAATACA T C GDI2 Ensembl:ENSG00000057608 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs996875350 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8335681 RMVar_hsa_circ_115518,RMVar_hsa_circ_141772,RMVar_hsa_circ_79431,RMVar_hsa_circ_141786,RMVar_hsa_circ_124483,RMVar_hsa_circ_268769,RMVar_hsa_circ_141789,RMVar_hsa_circ_362230 38343 RMVar_ID_38343 Human_SNP_ID_420393265 A-to-I Human chr10 - 5805584 5805584 5805584 CAAACCTTGCTTTGCAAGGCCAAGGCTGGGCTACATAGTGATATCCTGTTGCTACAAAAAATTAA CAAACCTTGCTTTGCAAGGCCAAGGCTGGGCTGCATAGTGATATCCTGTTGCTACAAAAAATTAA T C GDI2 Ensembl:ENSG00000057608 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1217916626 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115518,RMVar_hsa_circ_141772,RMVar_hsa_circ_79431,RMVar_hsa_circ_141786,RMVar_hsa_circ_124483,RMVar_hsa_circ_268769,RMVar_hsa_circ_141789,RMVar_hsa_circ_362230 38344 RMVar_ID_38344 Human_SNP_ID_420393970 A-to-I Human chr10 - 5808230 5808230 5808230 GCCTCAACCTTCCAGGCTCAAATGATCCTCCCACTTCAGCTTCCCAAGTTAGCTGGAACTACAGG GCCTCAACCTTCCAGGCTCAAATGATCCTCCCGCTTCAGCTTCCCAAGTTAGCTGGAACTACAGG T C GDI2 Ensembl:ENSG00000057608 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1226307970 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11377568 RMVar_hsa_circ_115518,RMVar_hsa_circ_141772,RMVar_hsa_circ_79431,RMVar_hsa_circ_141786,RMVar_hsa_circ_124483,RMVar_hsa_circ_268769,RMVar_hsa_circ_141789,RMVar_hsa_circ_362230 38345 RMVar_ID_38345 Human_SNP_ID_420408183 A-to-I Human chr10 - 5861355 5861355 5861355 CGGCTCACTGCAACCTCCGCCCCCTGGGTTCAAGTGATTTTTCTGCCTCAGCCTCCCAAGTAGCT CGGCTCACTGCAACCTCCGCCCCCTGGGTTCAGGTGATTTTTCTGCCTCAGCCTCCCAAGTAGCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913481932 Functional Loss SNV dbSNP153 33..33 33 - - - 38346 RMVar_ID_38346 Human_SNP_ID_420408439 A-to-I Human chr10 - 5862108 5862108 5862108 ATGAGGTCAGGAGATCGAGACCATCCTGGCTAACGTGGTGAAACCCCGTCTCTTACTAAAAATAC ATGAGGTCAGGAGATCGAGACCATCCTGGCTAGCGTGGTGAAACCCCGTCTCTTACTAAAAATAC T C RPL12P28,ANKRD16 Ensembl:ENSG00000240180,Ensembl:ENSG00000134461 Pseudogene,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs3209525 Functional Loss SNV dbSNP153 33..33 33 - - - 38347 RMVar_ID_38347 Human_SNP_ID_420411614 A-to-I Human chr10 - 5873231 5873231 5873231 TGTCTGGAGATCGAGACCATCCTGGCTAACACAGTGAAACCCTGTCTGTACTAAAAATACAAAAA TGTCTGGAGATCGAGACCATCCTGGCTAACACGGTGAAACCCTGTCTGTACTAAAAATACAAAAA T C ANKRD16 Ensembl:ENSG00000134461 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031454429 Functional Loss SNV dbSNP153 33..33 33 - - - 38348 RMVar_ID_38348 Human_SNP_ID_420411615 A-to-I Human chr10 - 5873231 5873231 5873231 TGTCTGGAGATCGAGACCATCCTGGCTAACACAGTGAAACCCTGTCTGTACTAAAAATACAAAAA TGTCTGGAGATCGAGACCATCCTGGCTAACACCGTGAAACCCTGTCTGTACTAAAAATACAAAAA T G ANKRD16 Ensembl:ENSG00000134461 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031454429 Functional Loss SNV dbSNP153 33..33 33 - - - 38349 RMVar_ID_38349 Human_SNP_ID_420415842 A-to-I Human chr10 - 5887888 5887888 5887888 GTACCTGCTCACTGTTTGCCCAGGTGCCTGGAAGACAGAGAGCAAAATTAGAAGGACTCCTCTGC GTACCTGCTCACTGTTTGCCCAGGTGCCTGGAGGACAGAGAGCAAAATTAGAAGGACTCCTCTGC T C ANKRD16 Ensembl:ENSG00000134461 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs775065911 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18431801,Human_RBP_ID_19045168 Human_Splice_Rec_1108873,Human_Splice_Rec_1108887,Human_Splice_Rec_1108899,Human_Splice_Rec_1108907 RMVar_hsa_circ_338981,RMVar_hsa_circ_19465 38350 RMVar_ID_38350 Human_SNP_ID_420417595 A-to-I Human chr10 + 5893159 5893159 5893159 GAAATCCTATCTCTACTAAAATACAAAAAATTAGCTGGCTGTGGCGGTGTGCACCTGTAGTCCCA GAAATCCTATCTCTACTAAAATACAAAAAATTTGCTGGCTGTGGCGGTGTGCACCTGTAGTCCCA A T FBH1 Ensembl:ENSG00000134452 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1564426569 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11378075 RMVar_hsa_circ_25048,RMVar_hsa_circ_104599,RMVar_hsa_circ_348344,RMVar_hsa_circ_141800,RMVar_hsa_circ_59483 38351 RMVar_ID_38351 Human_SNP_ID_420419637 A-to-I Human chr10 + 5901038 5901038 5901038 AAAATCACTTGAACCCAAGAGGTGAATGTTGCAGTGAGCCAAGATTGTGTCACTGTGCTCCAGCC AAAATCACTTGAACCCAAGAGGTGAATGTTGCCGTGAGCCAAGATTGTGTCACTGTGCTCCAGCC A C FBH1 Ensembl:ENSG00000134452 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1248431919 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17558880 RMVar_hsa_circ_25048,RMVar_hsa_circ_104599,RMVar_hsa_circ_348344,RMVar_hsa_circ_141800,RMVar_hsa_circ_59483 38352 RMVar_ID_38352 Human_SNP_ID_420419638 A-to-I Human chr10 + 5901038 5901038 5901038 AAAATCACTTGAACCCAAGAGGTGAATGTTGCAGTGAGCCAAGATTGTGTCACTGTGCTCCAGCC AAAATCACTTGAACCCAAGAGGTGAATGTTGCTGTGAGCCAAGATTGTGTCACTGTGCTCCAGCC A T FBH1 Ensembl:ENSG00000134452 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1248431919 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17558880 RMVar_hsa_circ_25048,RMVar_hsa_circ_104599,RMVar_hsa_circ_348344,RMVar_hsa_circ_141800,RMVar_hsa_circ_59483 38353 RMVar_ID_38353 Human_SNP_ID_420419682 A-to-I Human chr10 + 5901179 5901179 5901179 TGATACCATAGTTTAGTGGTGGAGTATTCTTTATTTTCTTTTTGAGATGGAGTTTCACTCTTGTT TGATACCATAGTTTAGTGGTGGAGTATTCTTTGTTTTCTTTTTGAGATGGAGTTTCACTCTTGTT A G FBH1 Ensembl:ENSG00000134452 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs989037173 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25048,RMVar_hsa_circ_104599,RMVar_hsa_circ_348344,RMVar_hsa_circ_141800,RMVar_hsa_circ_59483 38354 RMVar_ID_38354 Human_SNP_ID_420419825 A-to-I Human chr10 + 5901628 5901628 5901628 GTACTCTCGTCCAGGCTGGAGTGCAATGGCACAATCTTGGGTCACTACAACCTCCGCCTCCCGGG GTACTCTCGTCCAGGCTGGAGTGCAATGGCACGATCTTGGGTCACTACAACCTCCGCCTCCCGGG A G FBH1 Ensembl:ENSG00000134452 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs149029894 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25048,RMVar_hsa_circ_104599,RMVar_hsa_circ_348344,RMVar_hsa_circ_141800,RMVar_hsa_circ_59483 38355 RMVar_ID_38355 Human_SNP_ID_420419853 A-to-I Human chr10 + 5901737 5901737 5901737 CAGGTGCCCACCACCACACCTGGCTGATTTTTATATTTTTAGTAGAGATGGGGTTTCACCATGTT CAGGTGCCCACCACCACACCTGGCTGATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTT A G FBH1 Ensembl:ENSG00000134452 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1280606251 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25048,RMVar_hsa_circ_104599,RMVar_hsa_circ_348344,RMVar_hsa_circ_141800,RMVar_hsa_circ_59483 38356 RMVar_ID_38356 Human_SNP_ID_420419854 A-to-I Human chr10 + 5901745 5901745 5901745 CACCACCACACCTGGCTGATTTTTATATTTTTAGTAGAGATGGGGTTTCACCATGTTGCCAGGCT CACCACCACACCTGGCTGATTTTTATATTTTTGGTAGAGATGGGGTTTCACCATGTTGCCAGGCT A G FBH1 Ensembl:ENSG00000134452 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs983143479 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25048,RMVar_hsa_circ_104599,RMVar_hsa_circ_348344,RMVar_hsa_circ_141800,RMVar_hsa_circ_59483 38357 RMVar_ID_38357 Human_SNP_ID_420419858 A-to-I Human chr10 + 5901765 5901765 5901765 TTTTATATTTTTAGTAGAGATGGGGTTTCACCATGTTGCCAGGCTGGTCTTGAGCTCTAGACCTC TTTTATATTTTTAGTAGAGATGGGGTTTCACCGTGTTGCCAGGCTGGTCTTGAGCTCTAGACCTC A G FBH1 Ensembl:ENSG00000134452 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1010403688 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11378428 RMVar_hsa_circ_25048,RMVar_hsa_circ_104599,RMVar_hsa_circ_348344,RMVar_hsa_circ_141800,RMVar_hsa_circ_59483 38358 RMVar_ID_38358 Human_SNP_ID_420419869 A-to-I Human chr10 + 5901825 5901825 5901825 ACCTCAAGTGATCCACCCATCTTGGCCTCTCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCAC ACCTCAAGTGATCCACCCATCTTGGCCTCTCAGAGTGCTGGGATTACAGGCGTGAGCCACTGCAC A G FBH1 Ensembl:ENSG00000134452 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1268042172 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25048,RMVar_hsa_circ_104599,RMVar_hsa_circ_348344,RMVar_hsa_circ_141800,RMVar_hsa_circ_59483 38359 RMVar_ID_38359 Human_SNP_ID_420420564 A-to-I Human chr10 + 5904222 5904222 5904222 CCTAGCTAATTTTTGTATTTTTTTGTAGAGACAGGGTTTTGCTACGTTGCCCAGGCTGGTCTCAA CCTAGCTAATTTTTGTATTTTTTTGTAGAGACGGGGTTTTGCTACGTTGCCCAGGCTGGTCTCAA A G FBH1 Ensembl:ENSG00000134452 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1225793931 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104599,RMVar_hsa_circ_348344,RMVar_hsa_circ_141800,RMVar_hsa_circ_59483,RMVar_hsa_circ_141802,RMVar_hsa_circ_292928,RMVar_hsa_circ_317591,RMVar_hsa_circ_321002,RMVar_hsa_circ_378830,RMVar_hsa_circ_293495,RMVar_hsa_circ_61313,RMVar_hsa_circ_64634,RMVar_hsa_circ_141803,RMVar_hsa_circ_141801 38360 RMVar_ID_38360 Human_SNP_ID_420420664 A-to-I Human chr10 + 5904587 5904587 5904587 TTGGAAGATACCAGGATTTGGCTGGGAGCAGTAGCTCATGCCTTATTTGTAATCCCAGCAGTTTG TTGGAAGATACCAGGATTTGGCTGGGAGCAGTGGCTCATGCCTTATTTGTAATCCCAGCAGTTTG A G FBH1 Ensembl:ENSG00000134452 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs145601811 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104599,RMVar_hsa_circ_348344,RMVar_hsa_circ_141800,RMVar_hsa_circ_59483,RMVar_hsa_circ_141802,RMVar_hsa_circ_292928,RMVar_hsa_circ_317591,RMVar_hsa_circ_321002,RMVar_hsa_circ_378830,RMVar_hsa_circ_293495,RMVar_hsa_circ_61313,RMVar_hsa_circ_64634,RMVar_hsa_circ_141803,RMVar_hsa_circ_141801 38361 RMVar_ID_38361 Human_SNP_ID_420420665 A-to-I Human chr10 + 5904587 5904587 5904587 TTGGAAGATACCAGGATTTGGCTGGGAGCAGTAGCTCATGCCTTATTTGTAATCCCAGCAGTTTG TTGGAAGATACCAGGATTTGGCTGGGAGCAGTTGCTCATGCCTTATTTGTAATCCCAGCAGTTTG A T FBH1 Ensembl:ENSG00000134452 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs145601811 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104599,RMVar_hsa_circ_348344,RMVar_hsa_circ_141800,RMVar_hsa_circ_59483,RMVar_hsa_circ_141802,RMVar_hsa_circ_292928,RMVar_hsa_circ_317591,RMVar_hsa_circ_321002,RMVar_hsa_circ_378830,RMVar_hsa_circ_293495,RMVar_hsa_circ_61313,RMVar_hsa_circ_64634,RMVar_hsa_circ_141803,RMVar_hsa_circ_141801 38362 RMVar_ID_38362 Human_SNP_ID_420420830 A-to-I Human chr10 + 5905267 5905256 5905268 AGCTGGGCGCAGGGGCTCACGCCTGTAATGCCAGCACTTTGCGGGAGGCCGAGGTGAGTGGATTA AGCTGGGCGCAGGGGCTCACGC____________CACTTTGCGGGAGGCCGAGGTGAGTGGATTA CCTGTAATGCCAG C FBH1 Ensembl:ENSG00000134452 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1282104722 Functional Loss DEL dbSNP153 23..34 33 - - - Human_Splice_Rec_1109052,Human_Splice_Rec_1109053 RMVar_hsa_circ_104599,RMVar_hsa_circ_348344,RMVar_hsa_circ_141800,RMVar_hsa_circ_59483,RMVar_hsa_circ_141802,RMVar_hsa_circ_292928,RMVar_hsa_circ_317591,RMVar_hsa_circ_321002,RMVar_hsa_circ_378830,RMVar_hsa_circ_293495,RMVar_hsa_circ_61313,RMVar_hsa_circ_64634,RMVar_hsa_circ_141803,RMVar_hsa_circ_141801 38363 RMVar_ID_38363 Human_SNP_ID_420420860 A-to-I Human chr10 + 5905348 5905348 5905348 CTAGGCCAGCCTGGCCAACACGGCGAAACCCCATCTCTACTAAAATACAAAAATGAGCTAGGCAT CTAGGCCAGCCTGGCCAACACGGCGAAACCCCGTCTCTACTAAAATACAAAAATGAGCTAGGCAT A G FBH1 Ensembl:ENSG00000134452 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1301445686 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104599,RMVar_hsa_circ_348344,RMVar_hsa_circ_141800,RMVar_hsa_circ_59483,RMVar_hsa_circ_141802,RMVar_hsa_circ_292928,RMVar_hsa_circ_317591,RMVar_hsa_circ_321002,RMVar_hsa_circ_378830,RMVar_hsa_circ_293495,RMVar_hsa_circ_61313,RMVar_hsa_circ_64634,RMVar_hsa_circ_141803,RMVar_hsa_circ_141801 38364 RMVar_ID_38364 Human_SNP_ID_420420864 A-to-I Human chr10 + 5905362 5905362 5905362 CCAACACGGCGAAACCCCATCTCTACTAAAATACAAAAATGAGCTAGGCATGGTGGCATACGCCT CCAACACGGCGAAACCCCATCTCTACTAAAATGCAAAAATGAGCTAGGCATGGTGGCATACGCCT A G FBH1 Ensembl:ENSG00000134452 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1427141672 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104599,RMVar_hsa_circ_348344,RMVar_hsa_circ_141800,RMVar_hsa_circ_59483,RMVar_hsa_circ_141802,RMVar_hsa_circ_292928,RMVar_hsa_circ_317591,RMVar_hsa_circ_321002,RMVar_hsa_circ_378830,RMVar_hsa_circ_293495,RMVar_hsa_circ_61313,RMVar_hsa_circ_64634,RMVar_hsa_circ_141803,RMVar_hsa_circ_141801 38365 RMVar_ID_38365 Human_SNP_ID_420420865 A-to-I Human chr10 + 5905365 5905365 5905365 ACACGGCGAAACCCCATCTCTACTAAAATACAAAAATGAGCTAGGCATGGTGGCATACGCCTGTA ACACGGCGAAACCCCATCTCTACTAAAATACACAAATGAGCTAGGCATGGTGGCATACGCCTGTA A C FBH1 Ensembl:ENSG00000134452 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1419306223 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24817348 RMVar_hsa_circ_104599,RMVar_hsa_circ_348344,RMVar_hsa_circ_141800,RMVar_hsa_circ_59483,RMVar_hsa_circ_141802,RMVar_hsa_circ_292928,RMVar_hsa_circ_317591,RMVar_hsa_circ_321002,RMVar_hsa_circ_378830,RMVar_hsa_circ_293495,RMVar_hsa_circ_61313,RMVar_hsa_circ_64634,RMVar_hsa_circ_141803,RMVar_hsa_circ_141801 38366 RMVar_ID_38366 Human_SNP_ID_420420869 A-to-I Human chr10 + 5905389 5905389 5905389 AAAATACAAAAATGAGCTAGGCATGGTGGCATACGCCTGTAGTCCCAGCTACTTGGGAGGCTGAG AAAATACAAAAATGAGCTAGGCATGGTGGCATGCGCCTGTAGTCCCAGCTACTTGGGAGGCTGAG A G FBH1 Ensembl:ENSG00000134452 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs930635542 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104599,RMVar_hsa_circ_348344,RMVar_hsa_circ_141800,RMVar_hsa_circ_59483,RMVar_hsa_circ_141802,RMVar_hsa_circ_292928,RMVar_hsa_circ_317591,RMVar_hsa_circ_321002,RMVar_hsa_circ_378830,RMVar_hsa_circ_293495,RMVar_hsa_circ_61313,RMVar_hsa_circ_64634,RMVar_hsa_circ_141803,RMVar_hsa_circ_141801 38367 RMVar_ID_38367 Human_SNP_ID_420420874 A-to-I Human chr10 + 5905397 5905397 5905397 AAAATGAGCTAGGCATGGTGGCATACGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA AAAATGAGCTAGGCATGGTGGCATACGCCTGTCGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA A C FBH1 Ensembl:ENSG00000134452 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs148826073 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104599,RMVar_hsa_circ_348344,RMVar_hsa_circ_141800,RMVar_hsa_circ_59483,RMVar_hsa_circ_141802,RMVar_hsa_circ_292928,RMVar_hsa_circ_317591,RMVar_hsa_circ_321002,RMVar_hsa_circ_378830,RMVar_hsa_circ_293495,RMVar_hsa_circ_61313,RMVar_hsa_circ_64634,RMVar_hsa_circ_141803,RMVar_hsa_circ_141801 38368 RMVar_ID_38368 Human_SNP_ID_420428102 A-to-I Human chr10 + 5932781 5932781 5932781 GCTCTGTCACCCAGGCTGGAATATGGCGGCACAATCTTGGCCCACTGCAACCTCCGCCTCCCAGG GCTCTGTCACCCAGGCTGGAATATGGCGGCACGATCTTGGCCCACTGCAACCTCCGCCTCCCAGG A G FBH1 Ensembl:ENSG00000134452 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1466311331 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78713,RMVar_hsa_circ_141810 38369 RMVar_ID_38369 Human_SNP_ID_420428119 A-to-I Human chr10 + 5932847 5932847 5932847 TCAAGCCATCCTCCCACCTCAGCCTCCCGAGCAGCTGGGACTACAGGTGTGTGCCACCACACCTG TCAAGCCATCCTCCCACCTCAGCCTCCCGAGCCGCTGGGACTACAGGTGTGTGCCACCACACCTG A C FBH1 Ensembl:ENSG00000134452 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1333494672 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78713,RMVar_hsa_circ_141810 38370 RMVar_ID_38370 Human_SNP_ID_420476435 A-to-I Human chr10 + 6116719 6116719 6116719 GTTATTATGACATGAAAGTGTATCAAGAACTCAGCATTTCTTTGCATCCATGGACTTGGTTTGGA GTTATTATGACATGAAAGTGTATCAAGAACTCGGCATTTCTTTGCATCCATGGACTTGGTTTGGA A G RBM17 Ensembl:ENSG00000134453 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs554238997 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_273906,Human_RBP_ID_379476,Human_RBP_ID_1159187,Human_RBP_ID_1352209,Human_RBP_ID_1447889,Human_RBP_ID_1768067,Human_RBP_ID_3353013,Human_RBP_ID_8336119,Human_RBP_ID_11382339,Human_RBP_ID_17344094,Human_RBP_ID_17680324,Human_RBP_ID_23461402 Human_miRNA_ID_431775 38371 RMVar_ID_38371 Human_SNP_ID_420491683 A-to-I Human chr10 + 6171481 6171481 6171481 GCAGTGGCGCGATCTTGGCTCACTGCAGTCTCAACCTCCTGGGCTCAAGGAATCCTCCCGGCTCA GCAGTGGCGCGATCTTGGCTCACTGCAGTCTCTACCTCCTGGGCTCAAGGAATCCTCCCGGCTCA A T PFKFB3 Ensembl:ENSG00000170525 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404028132 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_141817,RMVar_hsa_circ_98825 38372 RMVar_ID_38372 Human_SNP_ID_420491705 A-to-I Human chr10 + 6171561 6171561 6171561 GGGACTATAGGCGTGTGCTGCCACACTCGGCTAATTTTATTTTTTGTAGAGATGAGGTCCCTCTG GGGACTATAGGCGTGTGCTGCCACACTCGGCTTATTTTATTTTTTGTAGAGATGAGGTCCCTCTG A T PFKFB3 Ensembl:ENSG00000170525 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1448980469 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9599619,Human_RBP_ID_11383306,Human_RBP_ID_22887574 RMVar_hsa_circ_141817,RMVar_hsa_circ_98825 38373 RMVar_ID_38373 Human_SNP_ID_420494881 A-to-I Human chr10 + 6181038 6181037 6181039 ATTTTATTTTCATTTGTAATTATTTTAGAGACAGAGTCTGGCTCTGTCGCTCAGGCTGGAGTGCA ATTTTATTTTCATTTGTAATTATTTTAGAGAC__AGTCTGGCTCTGTCGCTCAGGCTGGAGTGCA CAG C PFKFB3 Ensembl:ENSG00000170525 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs933368841 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_11383452 RMVar_hsa_circ_141817,RMVar_hsa_circ_98825 38374 RMVar_ID_38374 Human_SNP_ID_420494882 A-to-I Human chr10 + 6181038 6181038 6181038 ATTTTATTTTCATTTGTAATTATTTTAGAGACAGAGTCTGGCTCTGTCGCTCAGGCTGGAGTGCA ATTTTATTTTCATTTGTAATTATTTTAGAGACGGAGTCTGGCTCTGTCGCTCAGGCTGGAGTGCA A G PFKFB3 Ensembl:ENSG00000170525 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025474369 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11383452 RMVar_hsa_circ_141817,RMVar_hsa_circ_98825 38375 RMVar_ID_38375 Human_SNP_ID_420494903 A-to-I Human chr10 + 6181084 6181084 6181084 TCGCTCAGGCTGGAGTGCAGTGGTGCAGTCATAGTACACTGTAACCTCAAACTCCTGGGCTCAAG TCGCTCAGGCTGGAGTGCAGTGGTGCAGTCATGGTACACTGTAACCTCAAACTCCTGGGCTCAAG A G PFKFB3 Ensembl:ENSG00000170525 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs557402688 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_141817,RMVar_hsa_circ_98825 38376 RMVar_ID_38376 Human_SNP_ID_420494904 A-to-I Human chr10 + 6181094 6181094 6181094 TGGAGTGCAGTGGTGCAGTCATAGTACACTGTAACCTCAAACTCCTGGGCTCAAGCTATCGCCCC TGGAGTGCAGTGGTGCAGTCATAGTACACTGTGACCTCAAACTCCTGGGCTCAAGCTATCGCCCC A G PFKFB3 Ensembl:ENSG00000170525 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1033905029 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8336223 RMVar_hsa_circ_141817,RMVar_hsa_circ_98825 38377 RMVar_ID_38377 Human_SNP_ID_420494907 A-to-I Human chr10 + 6181119 6181119 6181119 ACACTGTAACCTCAAACTCCTGGGCTCAAGCTATCGCCCCACCTCAGCCTCCCAAGCAGCCAGTA ACACTGTAACCTCAAACTCCTGGGCTCAAGCTGTCGCCCCACCTCAGCCTCCCAAGCAGCCAGTA A G PFKFB3 Ensembl:ENSG00000170525 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1203949494 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8336223 RMVar_hsa_circ_141817,RMVar_hsa_circ_98825 38378 RMVar_ID_38378 Human_SNP_ID_420496007 A-to-I Human chr10 + 6184321 6184321 6184321 GTGATCTGCCTGCCTCAGCTCCACAAAGTGCTAGGATTACAGGTGTGAGCTACCACACCCAGCCT GTGATCTGCCTGCCTCAGCTCCACAAAGTGCTGGGATTACAGGTGTGAGCTACCACACCCAGCCT A G PFKFB3 Ensembl:ENSG00000170525 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031140203 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_141817,RMVar_hsa_circ_98825 38379 RMVar_ID_38379 Human_SNP_ID_420497932 A-to-I Human chr10 + 6190962 6190962 6190962 CAACATGCCCAGCTAATTTTTGTAGTTTTTGTAGAGATGGAGTTTCTCCATATTGGCCAGGCTGG CAACATGCCCAGCTAATTTTTGTAGTTTTTGTTGAGATGGAGTTTCTCCATATTGGCCAGGCTGG A T PFKFB3 Ensembl:ENSG00000170525 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1416685857 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_141817,RMVar_hsa_circ_98825 38380 RMVar_ID_38380 Human_SNP_ID_420499898 A-to-I Human chr10 + 6198506 6198505 6198507 ATTTGTAGAAAAATAATAATTTTTTTTGAGACAGAGTCTCGCTCTGTCACTCAGGCTGGAGTGCA ATTTGTAGAAAAATAATAATTTTTTTTGAGAC__AGTCTCGCTCTGTCACTCAGGCTGGAGTGCA CAG C PFKFB3 Ensembl:ENSG00000170525 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1234041597 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_141817,RMVar_hsa_circ_98825 38381 RMVar_ID_38381 Human_SNP_ID_420502108 A-to-I Human chr10 + 6205667 6205667 6205667 CGCCCACCTCAGCCTCCCAAAGTGCTGGGATTATAGGCATGAGCCACCACGCCCAGCTGGGTGGG CGCCCACCTCAGCCTCCCAAAGTGCTGGGATTGTAGGCATGAGCCACCACGCCCAGCTGGGTGGG A G PFKFB3 Ensembl:ENSG00000170525 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs574711408 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_141817,RMVar_hsa_circ_98825 38382 RMVar_ID_38382 Human_SNP_ID_420502110 A-to-I Human chr10 + 6205673 6205673 6205673 CCTCAGCCTCCCAAAGTGCTGGGATTATAGGCATGAGCCACCACGCCCAGCTGGGTGGGTTTTCT CCTCAGCCTCCCAAAGTGCTGGGATTATAGGCCTGAGCCACCACGCCCAGCTGGGTGGGTTTTCT A C PFKFB3 Ensembl:ENSG00000170525 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941004536 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_141817,RMVar_hsa_circ_98825 38383 RMVar_ID_38383 Human_SNP_ID_420504860 A-to-I Human chr10 + 6212700 6212700 6212700 AATTTATTTGTTTGTAGAGGCAGGGCCTTGCTATGTTGCCCAGGCTGGTCTCAAACTCATGGTCT AATTTATTTGTTTGTAGAGGCAGGGCCTTGCTGTGTTGCCCAGGCTGGTCTCAAACTCATGGTCT A G PFKFB3 Ensembl:ENSG00000170525 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1349111284 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_141817,RMVar_hsa_circ_98825 38384 RMVar_ID_38384 Human_SNP_ID_420504997 A-to-I Human chr10 + 6213265 6213265 6213265 AAATGAAAATTTCGATGAATGCTGGGTGTGGTAGCTATGCCTGTAATCCCAGCACTCTGGGAGGA AAATGAAAATTTCGATGAATGCTGGGTGTGGTGGCTATGCCTGTAATCCCAGCACTCTGGGAGGA A G PFKFB3 Ensembl:ENSG00000170525 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1180016366 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_141817,RMVar_hsa_circ_98825 38385 RMVar_ID_38385 Human_SNP_ID_420507217 A-to-I Human chr10 + 6220501 6220501 6220501 GCCAGACACCAGCTGTGGGAGTTGTCTTACGCATATGCTCTGCCCCTTAGAAGGATTCAGTCTGT GCCAGACACCAGCTGTGGGAGTTGTCTTACGCGTATGCTCTGCCCCTTAGAAGGATTCAGTCTGT A G PFKFB3 Ensembl:ENSG00000170525 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs969107884 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15369,RMVar_hsa_circ_376946,RMVar_hsa_circ_11006,RMVar_hsa_circ_14748,RMVar_hsa_circ_341234,RMVar_hsa_circ_297488,RMVar_hsa_circ_141821 38386 RMVar_ID_38386 Human_SNP_ID_420524759 A-to-I Human chr10 - 6283550 6283550 6283550 GCTCTTTCCTCTCATTCAGGGCTGAGTCTTCCAGCCTCCATCTTTCTCCCATGCTGGATGCTTCC GCTCTTTCCTCTCATTCAGGGCTGAGTCTTCCGGCCTCCATCTTTCTCCCATGCTGGATGCTTCC T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs5027484 Functional Loss SNV dbSNP153 33..33 33 - - - 38387 RMVar_ID_38387 Human_SNP_ID_420524760 A-to-I Human chr10 - 6283550 6283550 6283550 GCTCTTTCCTCTCATTCAGGGCTGAGTCTTCCAGCCTCCATCTTTCTCCCATGCTGGATGCTTCC GCTCTTTCCTCTCATTCAGGGCTGAGTCTTCCCGCCTCCATCTTTCTCCCATGCTGGATGCTTCC T G - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs5027484 Functional Loss SNV dbSNP153 33..33 33 - - - 38388 RMVar_ID_38388 Human_SNP_ID_420779617 A-to-I Human chr10 - 7245578 7245578 7245578 AGTCTTGGGCAAGTCAGTTAACTGCTCTGGGCATTAGTTCTGAGTCCTGTGGGTTATGGACTGGA AGTCTTGGGCAAGTCAGTTAACTGCTCTGGGCGTTAGTTCTGAGTCCTGTGGGTTATGGACTGGA T C SFMBT2 Ensembl:ENSG00000198879 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2692819 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_4342,GWAS_ID_4343,GWAS_ID_4344,GWAS_ID_4345,GWAS_ID_4346,GWAS_ID_4347,GWAS_ID_4348 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_282379,RMVar_hsa_circ_294917,RMVar_hsa_circ_141846,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_104180,RMVar_hsa_circ_289464,RMVar_hsa_circ_141851,RMVar_hsa_circ_141852,RMVar_hsa_circ_329598,RMVar_hsa_circ_272951,RMVar_hsa_circ_275052,RMVar_hsa_circ_141855,RMVar_hsa_circ_141857,RMVar_hsa_circ_141858,RMVar_hsa_circ_141856,RMVar_hsa_circ_141854 38389 RMVar_ID_38389 Human_SNP_ID_420791568 A-to-I Human chr10 - 7293250 7293250 7293250 TTCTAAAAATACAAAAATTAGCTGGATGTGGTAGGGCGTGCCTGTAGTCCCAGCTACTCGGGAAG TTCTAAAAATACAAAAATTAGCTGGATGTGGTGGGGCGTGCCTGTAGTCCCAGCTACTCGGGAAG T C SFMBT2 Ensembl:ENSG00000198879 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1289890645 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15750,RMVar_hsa_circ_317668,RMVar_hsa_circ_58187,RMVar_hsa_circ_2807,RMVar_hsa_circ_126640,RMVar_hsa_circ_361628,RMVar_hsa_circ_141842,RMVar_hsa_circ_141843,RMVar_hsa_circ_328246,RMVar_hsa_circ_104180,RMVar_hsa_circ_329598,RMVar_hsa_circ_141858,RMVar_hsa_circ_94735,RMVar_hsa_circ_353940,RMVar_hsa_circ_287262,RMVar_hsa_circ_128049,RMVar_hsa_circ_141863,RMVar_hsa_circ_141865,RMVar_hsa_circ_72660,RMVar_hsa_circ_141866,RMVar_hsa_circ_141864,RMVar_hsa_circ_63393,RMVar_hsa_circ_114208,RMVar_hsa_circ_75379,RMVar_hsa_circ_141869 38390 RMVar_ID_38390 Human_SNP_ID_420804731 A-to-I Human chr10 - 7344748 7344748 7344748 GGTTTTCACTGTGGTCTCGATCTCCTGACCTCATGATCCACCCTTCTTGGCCTCCCAAAGTGCTG GGTTTTCACTGTGGTCTCGATCTCCTGACCTCGTGATCCACCCTTCTTGGCCTCCCAAAGTGCTG T C SFMBT2 Ensembl:ENSG00000198879 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886553483 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15750,RMVar_hsa_circ_317668,RMVar_hsa_circ_58187,RMVar_hsa_circ_2807,RMVar_hsa_circ_126640,RMVar_hsa_circ_361628,RMVar_hsa_circ_141842,RMVar_hsa_circ_141843,RMVar_hsa_circ_328246,RMVar_hsa_circ_104180,RMVar_hsa_circ_329598,RMVar_hsa_circ_141858,RMVar_hsa_circ_94735,RMVar_hsa_circ_353940,RMVar_hsa_circ_287262,RMVar_hsa_circ_128049,RMVar_hsa_circ_141863,RMVar_hsa_circ_141865,RMVar_hsa_circ_72660,RMVar_hsa_circ_141866,RMVar_hsa_circ_141864,RMVar_hsa_circ_63393,RMVar_hsa_circ_114208,RMVar_hsa_circ_75379,RMVar_hsa_circ_141869,RMVar_hsa_circ_141870 38391 RMVar_ID_38391 Human_SNP_ID_420869436 A-to-I Human chr10 - 7582044 7582044 7582044 GGTGAAACCCGTCTCTACTAAAAAAGTACAAAAATTAGCCAGGCATGGTGGCGTGTGCCTGTAAT GGTGAAACCCGTCTCTACTAAAAAAGTACAAAGATTAGCCAGGCATGGTGGCGTGTGCCTGTAAT T C ITIH5 Ensembl:ENSG00000123243 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1333995498 Functional Loss SNV dbSNP153 33..33 33 - - - 38392 RMVar_ID_38392 Human_SNP_ID_420869437 A-to-I Human chr10 - 7582044 7582044 7582044 GGTGAAACCCGTCTCTACTAAAAAAGTACAAAAATTAGCCAGGCATGGTGGCGTGTGCCTGTAAT GGTGAAACCCGTCTCTACTAAAAAAGTACAAACATTAGCCAGGCATGGTGGCGTGTGCCTGTAAT T G ITIH5 Ensembl:ENSG00000123243 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1333995498 Functional Loss SNV dbSNP153 33..33 33 - - - 38393 RMVar_ID_38393 Human_SNP_ID_420869439 A-to-I Human chr10 - 7582052 7582050 7582052 GCCAACATGGTGAAACCCGTCTCTACTAAAAAAGTACAAAAATTAGCCAGGCATGGTGGCGTGTG GCCAACATGGTGAAACCCGTCTCTACTAAAAA__TACAAAAATTAGCCAGGCATGGTGGCGTGTG ACT A ITIH5 Ensembl:ENSG00000123243 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs921333169 Functional Loss DEL dbSNP153 33..34 33 - - - 38394 RMVar_ID_38394 Human_SNP_ID_420936947 A-to-I Human chr10 + 7832967 7832967 7832967 CTTGTAATCTTGTCACTTTGGGAGTCTGAGGCAGGAGGATGATTTGAGGCCAGGAGTTCGAGATA CTTGTAATCTTGTCACTTTGGGAGTCTGAGGCGGGAGGATGATTTGAGGCCAGGAGTTCGAGATA A G TAF3 Ensembl:ENSG00000165632 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1398738050 Functional Loss SNV dbSNP153 33..33 33 - - - 38395 RMVar_ID_38395 Human_SNP_ID_420949051 A-to-I Human chr10 + 7878750 7878750 7878750 TATGTATGTATGTATGTATGTATGTATATGAGACAGAGTCTTGCTCTGTTGCTCAGGCTGGAGTG TATGTATGTATGTATGTATGTATGTATATGAGTCAGAGTCTTGCTCTGTTGCTCAGGCTGGAGTG A T TAF3 Ensembl:ENSG00000165632 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1158219323 Functional Loss SNV dbSNP153 33..33 33 - - - 38396 RMVar_ID_38396 Human_SNP_ID_421575984 A-to-I Human chr10 - 10284712 10284712 10284712 CCTCAGCCTCCTGAGTAGCTGGGACTACAGGCACCCACCACCACGCCCAGCTAATTTTTACATTT CCTCAGCCTCCTGAGTAGCTGGGACTACAGGCGCCCACCACCACGCCCAGCTAATTTTTACATTT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs572069771 Functional Loss SNV dbSNP153 33..33 33 - - - 38397 RMVar_ID_38397 Human_SNP_ID_421749252 A-to-I Human chr10 - 10941872 10941872 10941872 CTTCTGCCCCAGCCTCCCCAGTGGCTGGGATTACAGGCACCTGCCACCACACCTGGCTAATTTTT CTTCTGCCCCAGCCTCCCCAGTGGCTGGGATTTCAGGCACCTGCCACCACACCTGGCTAATTTTT T A LINC00710 Ensembl:ENSG00000229240 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903361284 Functional Loss SNV dbSNP153 33..33 33 - - - 38398 RMVar_ID_38398 Human_SNP_ID_421751630 A-to-I Human chr10 - 10951272 10951272 10951272 GGGTGTGGTGGTGCATGCCTGTGGTCCCAGCTACTCAGAAAGCCAAGGTGGGAGGATGGCTTGAG GGGTGTGGTGGTGCATGCCTGTGGTCCCAGCTGCTCAGAAAGCCAAGGTGGGAGGATGGCTTGAG T C LINC00710 Ensembl:ENSG00000229240 lincRNA intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs985226707 Functional Loss SNV dbSNP153 33..33 33 - - - 38399 RMVar_ID_38399 Human_SNP_ID_421773076 A-to-I Human chr10 + 11037383 11037381 11037384 GGGTCATTACAATTCAAGGTGAGATTTGTGTGAGGACACAGCCAAACCATATCGACCACTGTATC GGGTCATTACAATTCAAGGTGAGATTTGTGT___GACACAGCCAAACCATATCGACCACTGTATC TGAG T CELF2 Ensembl:ENSG00000048740 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1380987420 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_40847,RMVar_hsa_circ_45624,RMVar_hsa_circ_317993,RMVar_hsa_circ_314771,RMVar_hsa_circ_32203 38400 RMVar_ID_38400 Human_SNP_ID_421786121 A-to-I Human chr10 + 11085963 11085963 11085963 CGGCCCATCTGTAAACTGAGGAAAGCGACAGTACCAATAACAAGTTCATTGTGATGGATTTAATG CGGCCCATCTGTAAACTGAGGAAAGCGACAGTGCCAATAACAAGTTCATTGTGATGGATTTAATG A G CELF2 Ensembl:ENSG00000048740 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1248482125 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40847,RMVar_hsa_circ_45624,RMVar_hsa_circ_317993,RMVar_hsa_circ_314771,RMVar_hsa_circ_32203 38401 RMVar_ID_38401 Human_SNP_ID_421786168 A-to-I Human chr10 + 11086143 11086143 11086143 GTGTTCTAATACACGGGATCAAATCTATAGGTACCCACTGTTTTTCAATGAACAGGATTATTCAG GTGTTCTAATACACGGGATCAAATCTATAGGTGCCCACTGTTTTTCAATGAACAGGATTATTCAG A G CELF2 Ensembl:ENSG00000048740 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs752864938 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40847,RMVar_hsa_circ_45624,RMVar_hsa_circ_317993,RMVar_hsa_circ_314771,RMVar_hsa_circ_32203 38402 RMVar_ID_38402 Human_SNP_ID_421786169 A-to-I Human chr10 + 11086143 11086143 11086143 GTGTTCTAATACACGGGATCAAATCTATAGGTACCCACTGTTTTTCAATGAACAGGATTATTCAG GTGTTCTAATACACGGGATCAAATCTATAGGTTCCCACTGTTTTTCAATGAACAGGATTATTCAG A T CELF2 Ensembl:ENSG00000048740 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs752864938 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40847,RMVar_hsa_circ_45624,RMVar_hsa_circ_317993,RMVar_hsa_circ_314771,RMVar_hsa_circ_32203 38403 RMVar_ID_38403 Human_SNP_ID_421810268 A-to-I Human chr10 + 11174959 11174959 11174959 GAATTGCTATCAATTTTAATACCTCCCTACTAAACATTCTGTGTAGGGGATGCCTTAGTAATCTG GAATTGCTATCAATTTTAATACCTCCCTACTACACATTCTGTGTAGGGGATGCCTTAGTAATCTG A C CELF2 Ensembl:ENSG00000048740 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1236638861 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40847,RMVar_hsa_circ_45624,RMVar_hsa_circ_314771,RMVar_hsa_circ_32203,RMVar_hsa_circ_1165,RMVar_hsa_circ_297045,RMVar_hsa_circ_305567,RMVar_hsa_circ_315228,RMVar_hsa_circ_316652,RMVar_hsa_circ_314061,RMVar_hsa_circ_34250,RMVar_hsa_circ_270630,RMVar_hsa_circ_16892,RMVar_hsa_circ_141973,RMVar_hsa_circ_141975,RMVar_hsa_circ_141976,RMVar_hsa_circ_141977,RMVar_hsa_circ_141974 38404 RMVar_ID_38404 Human_SNP_ID_421815247 A-to-I Human chr10 + 11192896 11192896 11192896 TGAAGGTATTGAGGTGATTCTAACGTGCAGCCAAGGTTGAGAAGGACCAAGCTGGACGTTGCGAG TGAAGGTATTGAGGTGATTCTAACGTGCAGCCGAGGTTGAGAAGGACCAAGCTGGACGTTGCGAG A G CELF2 Ensembl:ENSG00000048740 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1998860 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40847,RMVar_hsa_circ_45624,RMVar_hsa_circ_314771,RMVar_hsa_circ_32203,RMVar_hsa_circ_1165,RMVar_hsa_circ_297045,RMVar_hsa_circ_305567,RMVar_hsa_circ_315228,RMVar_hsa_circ_316652,RMVar_hsa_circ_314061,RMVar_hsa_circ_34250,RMVar_hsa_circ_270630,RMVar_hsa_circ_16892,RMVar_hsa_circ_141973,RMVar_hsa_circ_141975,RMVar_hsa_circ_141976,RMVar_hsa_circ_141977,RMVar_hsa_circ_141974 38405 RMVar_ID_38405 Human_SNP_ID_422017918 A-to-I Human chr10 - 11957057 11957057 11957057 CCAGCACTTTGGGAGGCCAAGGCACAGGGATTACTTGACGTCGGCGTTGGAGGCCAGCCTGGGCA CCAGCACTTTGGGAGGCCAAGGCACAGGGATTCCTTGACGTCGGCGTTGGAGGCCAGCCTGGGCA T G UPF2 Ensembl:ENSG00000151461 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs774357003 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26384,RMVar_hsa_circ_95739,RMVar_hsa_circ_376799,RMVar_hsa_circ_112605,RMVar_hsa_circ_50367,RMVar_hsa_circ_73176,RMVar_hsa_circ_142053,RMVar_hsa_circ_142055,RMVar_hsa_circ_5884,RMVar_hsa_circ_142054,RMVar_hsa_circ_142052,RMVar_hsa_circ_368908,RMVar_hsa_circ_372718,RMVar_hsa_circ_64973,RMVar_hsa_circ_142058,RMVar_hsa_circ_363546,RMVar_hsa_circ_321643,RMVar_hsa_circ_51700,RMVar_hsa_circ_45644,RMVar_hsa_circ_351211,RMVar_hsa_circ_142059,RMVar_hsa_circ_367929,RMVar_hsa_circ_368352,RMVar_hsa_circ_359204,RMVar_hsa_circ_314519,RMVar_hsa_circ_350494,RMVar_hsa_circ_142063,RMVar_hsa_circ_321020,RMVar_hsa_circ_350884,RMVar_hsa_circ_142062,RMVar_hsa_circ_296015,RMVar_hsa_circ_357679,RMVar_hsa_circ_368869,RMVar_hsa_circ_299147,RMVar_hsa_circ_142065,RMVar_hsa_circ_34065,RMVar_hsa_circ_142064,RMVar_hsa_circ_306240 38406 RMVar_ID_38406 Human_SNP_ID_422019562 A-to-I Human chr10 - 11963537 11963537 11963537 CAGCACTTACAAAATACCAGCCTTGGCAACATAGTGAGACCTCCTCTCTACAAACACATTTTAGA CAGCACTTACAAAATACCAGCCTTGGCAACATTGTGAGACCTCCTCTCTACAAACACATTTTAGA T A UPF2 Ensembl:ENSG00000151461 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334817440 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95739,RMVar_hsa_circ_376799,RMVar_hsa_circ_112605,RMVar_hsa_circ_50367,RMVar_hsa_circ_73176,RMVar_hsa_circ_142053,RMVar_hsa_circ_142055,RMVar_hsa_circ_5884,RMVar_hsa_circ_142054,RMVar_hsa_circ_142052,RMVar_hsa_circ_368908,RMVar_hsa_circ_64973,RMVar_hsa_circ_363546,RMVar_hsa_circ_321643,RMVar_hsa_circ_51700,RMVar_hsa_circ_45644,RMVar_hsa_circ_351211,RMVar_hsa_circ_142059,RMVar_hsa_circ_367929,RMVar_hsa_circ_368352,RMVar_hsa_circ_314519,RMVar_hsa_circ_350494,RMVar_hsa_circ_142063,RMVar_hsa_circ_350884,RMVar_hsa_circ_296015,RMVar_hsa_circ_357679,RMVar_hsa_circ_299147,RMVar_hsa_circ_142065,RMVar_hsa_circ_34065,RMVar_hsa_circ_306240,RMVar_hsa_circ_34501 38407 RMVar_ID_38407 Human_SNP_ID_422019563 A-to-I Human chr10 - 11963537 11963537 11963537 CAGCACTTACAAAATACCAGCCTTGGCAACATAGTGAGACCTCCTCTCTACAAACACATTTTAGA CAGCACTTACAAAATACCAGCCTTGGCAACATCGTGAGACCTCCTCTCTACAAACACATTTTAGA T G UPF2 Ensembl:ENSG00000151461 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334817440 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95739,RMVar_hsa_circ_376799,RMVar_hsa_circ_112605,RMVar_hsa_circ_50367,RMVar_hsa_circ_73176,RMVar_hsa_circ_142053,RMVar_hsa_circ_142055,RMVar_hsa_circ_5884,RMVar_hsa_circ_142054,RMVar_hsa_circ_142052,RMVar_hsa_circ_368908,RMVar_hsa_circ_64973,RMVar_hsa_circ_363546,RMVar_hsa_circ_321643,RMVar_hsa_circ_51700,RMVar_hsa_circ_45644,RMVar_hsa_circ_351211,RMVar_hsa_circ_142059,RMVar_hsa_circ_367929,RMVar_hsa_circ_368352,RMVar_hsa_circ_314519,RMVar_hsa_circ_350494,RMVar_hsa_circ_142063,RMVar_hsa_circ_350884,RMVar_hsa_circ_296015,RMVar_hsa_circ_357679,RMVar_hsa_circ_299147,RMVar_hsa_circ_142065,RMVar_hsa_circ_34065,RMVar_hsa_circ_306240,RMVar_hsa_circ_34501 38408 RMVar_ID_38408 Human_SNP_ID_422023518 A-to-I Human chr10 - 11979128 11979128 11979128 ATTTGCTACCATTTTATGCAAGATTGGTTGCTACATTGCATCCCTGCATGTCTGATGTAGCAGAG ATTTGCTACCATTTTATGCAAGATTGGTTGCTGCATTGCATCCCTGCATGTCTGATGTAGCAGAG T C UPF2 Ensembl:ENSG00000151461 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1441379108 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1112410,Human_Splice_Rec_1112411,Human_Splice_Rec_1112452,Human_Splice_Rec_1112453,Human_Splice_Rec_1112494,Human_Splice_Rec_1112495 RMVar_hsa_circ_95739,RMVar_hsa_circ_112605,RMVar_hsa_circ_50367,RMVar_hsa_circ_73176,RMVar_hsa_circ_142053,RMVar_hsa_circ_142055,RMVar_hsa_circ_5884,RMVar_hsa_circ_142054,RMVar_hsa_circ_368908,RMVar_hsa_circ_321643,RMVar_hsa_circ_51700,RMVar_hsa_circ_142067,RMVar_hsa_circ_45644,RMVar_hsa_circ_351211,RMVar_hsa_circ_142059,RMVar_hsa_circ_367929,RMVar_hsa_circ_350494,RMVar_hsa_circ_142063,RMVar_hsa_circ_350884,RMVar_hsa_circ_63612,RMVar_hsa_circ_296015,RMVar_hsa_circ_34065,RMVar_hsa_circ_306240,RMVar_hsa_circ_274001,RMVar_hsa_circ_358478,RMVar_hsa_circ_368418,RMVar_hsa_circ_34501,RMVar_hsa_circ_361837,RMVar_hsa_circ_329431,RMVar_hsa_circ_335080,RMVar_hsa_circ_371370,RMVar_hsa_circ_285612,RMVar_hsa_circ_55897,RMVar_hsa_circ_59434,RMVar_hsa_circ_142069,RMVar_hsa_circ_142068,RMVar_hsa_circ_142070,RMVar_hsa_circ_105853,RMVar_hsa_circ_288763,RMVar_hsa_circ_142066,RMVar_hsa_circ_360130,RMVar_hsa_circ_277949,RMVar_hsa_circ_142071 38409 RMVar_ID_38409 Human_SNP_ID_422031095 A-to-I Human chr10 - 12007968 12007968 12007968 TGAAGTGAGACAATTGCTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCTGAGATTGCACTCCAGC TGAAGTGAGACAATTGCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCTGAGATTGCACTCCAGC T C UPF2 Ensembl:ENSG00000151461 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs745396845 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3978,RMVar_hsa_circ_95739,RMVar_hsa_circ_50367,RMVar_hsa_circ_73176,RMVar_hsa_circ_142055,RMVar_hsa_circ_368908,RMVar_hsa_circ_321643,RMVar_hsa_circ_351211,RMVar_hsa_circ_142059,RMVar_hsa_circ_350494,RMVar_hsa_circ_142063,RMVar_hsa_circ_350884,RMVar_hsa_circ_63612,RMVar_hsa_circ_296015,RMVar_hsa_circ_306240,RMVar_hsa_circ_274001,RMVar_hsa_circ_285612,RMVar_hsa_circ_59434,RMVar_hsa_circ_142069,RMVar_hsa_circ_142070,RMVar_hsa_circ_288763,RMVar_hsa_circ_360130,RMVar_hsa_circ_142075,RMVar_hsa_circ_273559,RMVar_hsa_circ_329449,RMVar_hsa_circ_142077,RMVar_hsa_circ_94125,RMVar_hsa_circ_142076,RMVar_hsa_circ_332481,RMVar_hsa_circ_333545 38410 RMVar_ID_38410 Human_SNP_ID_422031117 A-to-I Human chr10 - 12008071 12008071 12008071 CTAGACCAGCCTGGCCAACATGGTGAAACCCCATCCCTACAAAAAATACAAAAGTTAGCTGGGTA CTAGACCAGCCTGGCCAACATGGTGAAACCCCGTCCCTACAAAAAATACAAAAGTTAGCTGGGTA T C UPF2 Ensembl:ENSG00000151461 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1323516425 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3978,RMVar_hsa_circ_95739,RMVar_hsa_circ_50367,RMVar_hsa_circ_73176,RMVar_hsa_circ_142055,RMVar_hsa_circ_368908,RMVar_hsa_circ_321643,RMVar_hsa_circ_351211,RMVar_hsa_circ_142059,RMVar_hsa_circ_350494,RMVar_hsa_circ_142063,RMVar_hsa_circ_350884,RMVar_hsa_circ_63612,RMVar_hsa_circ_296015,RMVar_hsa_circ_306240,RMVar_hsa_circ_274001,RMVar_hsa_circ_285612,RMVar_hsa_circ_59434,RMVar_hsa_circ_142069,RMVar_hsa_circ_142070,RMVar_hsa_circ_288763,RMVar_hsa_circ_360130,RMVar_hsa_circ_142075,RMVar_hsa_circ_273559,RMVar_hsa_circ_329449,RMVar_hsa_circ_142077,RMVar_hsa_circ_94125,RMVar_hsa_circ_142076,RMVar_hsa_circ_332481,RMVar_hsa_circ_333545 38411 RMVar_ID_38411 Human_SNP_ID_422031892 A-to-I Human chr10 - 12011192 12011192 12011192 TGAGGCGAGTTTGAGACTAGCCTGGGTAACATAGCGAGACCCTGTCTCTACAAAAAATTTTAAAA TGAGGCGAGTTTGAGACTAGCCTGGGTAACATGGCGAGACCCTGTCTCTACAAAAAATTTTAAAA T C UPF2 Ensembl:ENSG00000151461 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1355573434 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3978,RMVar_hsa_circ_95739,RMVar_hsa_circ_50367,RMVar_hsa_circ_73176,RMVar_hsa_circ_142055,RMVar_hsa_circ_368908,RMVar_hsa_circ_321643,RMVar_hsa_circ_351211,RMVar_hsa_circ_142059,RMVar_hsa_circ_350494,RMVar_hsa_circ_142063,RMVar_hsa_circ_350884,RMVar_hsa_circ_63612,RMVar_hsa_circ_296015,RMVar_hsa_circ_306240,RMVar_hsa_circ_274001,RMVar_hsa_circ_285612,RMVar_hsa_circ_59434,RMVar_hsa_circ_142069,RMVar_hsa_circ_142070,RMVar_hsa_circ_288763,RMVar_hsa_circ_360130,RMVar_hsa_circ_142075,RMVar_hsa_circ_273559,RMVar_hsa_circ_329449,RMVar_hsa_circ_142077,RMVar_hsa_circ_94125,RMVar_hsa_circ_142076,RMVar_hsa_circ_332481,RMVar_hsa_circ_333545 38412 RMVar_ID_38412 Human_SNP_ID_422034160 A-to-I Human chr10 - 12019862 12019862 12019862 AAATTAGCCGGGTGTGGTGGCAGGCTCCTGTAATCCCAGCTATGTGGGAGGCTGAGGCAGGGAGA AAATTAGCCGGGTGTGGTGGCAGGCTCCTGTAGTCCCAGCTATGTGGGAGGCTGAGGCAGGGAGA T C UPF2 Ensembl:ENSG00000151461 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1436427996 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95739,RMVar_hsa_circ_73176,RMVar_hsa_circ_142055,RMVar_hsa_circ_351211,RMVar_hsa_circ_63612,RMVar_hsa_circ_59434,RMVar_hsa_circ_360130,RMVar_hsa_circ_329449,RMVar_hsa_circ_142077,RMVar_hsa_circ_94125,RMVar_hsa_circ_142076,RMVar_hsa_circ_370792,RMVar_hsa_circ_142080 38413 RMVar_ID_38413 Human_SNP_ID_422034575 A-to-I Human chr10 - 12021483 12021483 12021483 GGGTCTTTCCCTGTCACCCAGGCTGGAGTGTCATGGTGCAGTCATAGCTCACTGCAGCCTCGCTA GGGTCTTTCCCTGTCACCCAGGCTGGAGTGTCGTGGTGCAGTCATAGCTCACTGCAGCCTCGCTA T C UPF2 Ensembl:ENSG00000151461 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs570544635 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5935212 RMVar_hsa_circ_95739,RMVar_hsa_circ_73176,RMVar_hsa_circ_142055,RMVar_hsa_circ_351211,RMVar_hsa_circ_63612,RMVar_hsa_circ_59434,RMVar_hsa_circ_360130,RMVar_hsa_circ_329449,RMVar_hsa_circ_142077,RMVar_hsa_circ_94125,RMVar_hsa_circ_142076,RMVar_hsa_circ_370792,RMVar_hsa_circ_142080 38414 RMVar_ID_38414 Human_SNP_ID_422034708 A-to-I Human chr10 - 12021974 12021974 12021974 CACCACACTCGACTAATTTTTGTATTTTTAGCAGAGACAGGGTTTCACCATGTTGGCCAGGCTGG CACCACACTCGACTAATTTTTGTATTTTTAGCGGAGACAGGGTTTCACCATGTTGGCCAGGCTGG T C UPF2 Ensembl:ENSG00000151461 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs181081479 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95739,RMVar_hsa_circ_73176,RMVar_hsa_circ_142055,RMVar_hsa_circ_351211,RMVar_hsa_circ_63612,RMVar_hsa_circ_59434,RMVar_hsa_circ_360130,RMVar_hsa_circ_329449,RMVar_hsa_circ_142077,RMVar_hsa_circ_94125,RMVar_hsa_circ_142076,RMVar_hsa_circ_370792,RMVar_hsa_circ_142080 38415 RMVar_ID_38415 Human_SNP_ID_422034726 A-to-I Human chr10 - 12022018 12022018 12022018 CTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACATGCACCTGCCACCACACTCGACTAATTTTT CTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTGCATGCACCTGCCACCACACTCGACTAATTTTT T C UPF2 Ensembl:ENSG00000151461 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1168391758 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95739,RMVar_hsa_circ_73176,RMVar_hsa_circ_142055,RMVar_hsa_circ_351211,RMVar_hsa_circ_63612,RMVar_hsa_circ_59434,RMVar_hsa_circ_360130,RMVar_hsa_circ_329449,RMVar_hsa_circ_142077,RMVar_hsa_circ_94125,RMVar_hsa_circ_142076,RMVar_hsa_circ_370792,RMVar_hsa_circ_142080 38416 RMVar_ID_38416 Human_SNP_ID_422034797 A-to-I Human chr10 - 12022240 12022238 12022240 GCCTGGCTAATTTTTTGTGTTTTAGAAGAGACAGGGTTTCACCATGTTGCCCAGGCTGGTCTCGA GCCTGGCTAATTTTTTGTGTTTTAGAAGAGAC__GGTTTCACCATGTTGCCCAGGCTGGTCTCGA CCT C UPF2 Ensembl:ENSG00000151461 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1489963593 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_95739,RMVar_hsa_circ_73176,RMVar_hsa_circ_142055,RMVar_hsa_circ_351211,RMVar_hsa_circ_63612,RMVar_hsa_circ_59434,RMVar_hsa_circ_360130,RMVar_hsa_circ_329449,RMVar_hsa_circ_142077,RMVar_hsa_circ_94125,RMVar_hsa_circ_142076,RMVar_hsa_circ_370792,RMVar_hsa_circ_142080 38417 RMVar_ID_38417 Human_SNP_ID_422035087 A-to-I Human chr10 - 12023424 12023424 12023424 ATGATCTTCCCGCCTCGGCCTCCCAAAGTGCTAGGATTACAGGTGTGATCCACCATGCCCAGCCG ATGATCTTCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGATCCACCATGCCCAGCCG T C UPF2 Ensembl:ENSG00000151461 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs936391055 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95739,RMVar_hsa_circ_73176,RMVar_hsa_circ_142055,RMVar_hsa_circ_351211,RMVar_hsa_circ_63612,RMVar_hsa_circ_59434,RMVar_hsa_circ_360130,RMVar_hsa_circ_329449,RMVar_hsa_circ_142077,RMVar_hsa_circ_94125,RMVar_hsa_circ_142076,RMVar_hsa_circ_370792,RMVar_hsa_circ_142080 38418 RMVar_ID_38418 Human_SNP_ID_422035267 A-to-I Human chr10 - 12023975 12023975 12023975 TATTTTATTTTGTTTTTTTGAGACAAGGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGCAGG TATTTTATTTTGTTTTTTTGAGACAAGGTCTCGCTCTGTCACCCAGGCTGGAGTGCAGTGGCAGG T C UPF2 Ensembl:ENSG00000151461 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs534068809 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95739,RMVar_hsa_circ_73176,RMVar_hsa_circ_142055,RMVar_hsa_circ_351211,RMVar_hsa_circ_63612,RMVar_hsa_circ_59434,RMVar_hsa_circ_360130,RMVar_hsa_circ_329449,RMVar_hsa_circ_142077,RMVar_hsa_circ_94125,RMVar_hsa_circ_142076,RMVar_hsa_circ_370792,RMVar_hsa_circ_142080 38419 RMVar_ID_38419 Human_SNP_ID_422036115 A-to-I Human chr10 - 12026762 12026762 12026762 GGTAATCCCAGCTACTTGTGGGGGACTGAGGCAGGAGAATCACTTGACCCTGGGAGGTGGAGGTT GGTAATCCCAGCTACTTGTGGGGGACTGAGGCCGGAGAATCACTTGACCCTGGGAGGTGGAGGTT T G UPF2 Ensembl:ENSG00000151461 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982624453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_371682,Human_RBP_ID_11278047 RMVar_hsa_circ_95739,RMVar_hsa_circ_73176,RMVar_hsa_circ_142055,RMVar_hsa_circ_351211,RMVar_hsa_circ_63612,RMVar_hsa_circ_59434,RMVar_hsa_circ_360130,RMVar_hsa_circ_329449,RMVar_hsa_circ_142077,RMVar_hsa_circ_94125,RMVar_hsa_circ_142076,RMVar_hsa_circ_370792,RMVar_hsa_circ_142080 38420 RMVar_ID_38420 Human_SNP_ID_422036121 A-to-I Human chr10 - 12026785 12026785 12026785 AGCCGGGCATGGTGGCAGGCCCCGGTAATCCCAGCTACTTGTGGGGGACTGAGGCAGGAGAATCA AGCCGGGCATGGTGGCAGGCCCCGGTAATCCCCGCTACTTGTGGGGGACTGAGGCAGGAGAATCA T G UPF2 Ensembl:ENSG00000151461 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1192069086 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95739,RMVar_hsa_circ_73176,RMVar_hsa_circ_142055,RMVar_hsa_circ_351211,RMVar_hsa_circ_63612,RMVar_hsa_circ_59434,RMVar_hsa_circ_360130,RMVar_hsa_circ_329449,RMVar_hsa_circ_142077,RMVar_hsa_circ_94125,RMVar_hsa_circ_142076,RMVar_hsa_circ_370792,RMVar_hsa_circ_142080 38421 RMVar_ID_38421 Human_SNP_ID_422038948 A-to-I Human chr10 - 12037290 12037290 12037290 ATCACTTAAACTCAGGATTTCGAGACCAGCCTAGTCAACATGGGGAAATCCCATCTCTACTAAAA ATCACTTAAACTCAGGATTTCGAGACCAGCCTGGTCAACATGGGGAAATCCCATCTCTACTAAAA T C UPF2 Ensembl:ENSG00000151461 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1201467607 Functional Loss SNV dbSNP153 33..33 33 - - - 38422 RMVar_ID_38422 Human_SNP_ID_422049242 A-to-I Human chr10 + 12071516 12071516 12071516 TTATTAGGCCGGGCGCGGTGGCTCATGCCTGTAATCCCTGCACTTTGGGAGGCCGAGGTGGGCGG TTATTAGGCCGGGCGCGGTGGCTCATGCCTGTGATCCCTGCACTTTGGGAGGCCGAGGTGGGCGG A G DHTKD1 Ensembl:ENSG00000181192 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1171854697 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98961,RMVar_hsa_circ_115171,RMVar_hsa_circ_142084,RMVar_hsa_circ_79404,RMVar_hsa_circ_142085,RMVar_hsa_circ_142083 38423 RMVar_ID_38423 Human_SNP_ID_422049434 A-to-I Human chr10 + 12072257 12072257 12072257 GGGAGGCCGAGCTGGGAAGATCACTTGAGGCCAGAAGTTCCAGGCCAGCCTGGCTGACATGGTGA GGGAGGCCGAGCTGGGAAGATCACTTGAGGCCGGAAGTTCCAGGCCAGCCTGGCTGACATGGTGA A G DHTKD1 Ensembl:ENSG00000181192 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs923187955 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98961,RMVar_hsa_circ_115171,RMVar_hsa_circ_142084,RMVar_hsa_circ_79404,RMVar_hsa_circ_142085,RMVar_hsa_circ_142083 38424 RMVar_ID_38424 Human_SNP_ID_422049440 A-to-I Human chr10 + 12072296 12072296 12072296 CCAGGCCAGCCTGGCTGACATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTGACCTGGTG CCAGGCCAGCCTGGCTGACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTGACCTGGTG A G DHTKD1 Ensembl:ENSG00000181192 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs12263793 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98961,RMVar_hsa_circ_115171,RMVar_hsa_circ_142084,RMVar_hsa_circ_79404,RMVar_hsa_circ_142085,RMVar_hsa_circ_142083 38425 RMVar_ID_38425 Human_SNP_ID_422049446 A-to-I Human chr10 + 12072339 12072339 12072339 AAATACAAAAATTGACCTGGTGGTGTGTGCCTATAATACCGGTTACTCGGGAGGCTGAGTCAGGA AAATACAAAAATTGACCTGGTGGTGTGTGCCTGTAATACCGGTTACTCGGGAGGCTGAGTCAGGA A G DHTKD1 Ensembl:ENSG00000181192 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs906076202 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98961,RMVar_hsa_circ_115171,RMVar_hsa_circ_142084,RMVar_hsa_circ_79404,RMVar_hsa_circ_142085,RMVar_hsa_circ_142083 38426 RMVar_ID_38426 Human_SNP_ID_422050114 A-to-I Human chr10 + 12074565 12074565 12074565 TTTTTTTAGTAGAGATGGGGTTTCACCGTGTTAGCCAGGATGGTTTCGATCTCTTGACCTCATGA TTTTTTTAGTAGAGATGGGGTTTCACCGTGTTCGCCAGGATGGTTTCGATCTCTTGACCTCATGA A C DHTKD1 Ensembl:ENSG00000181192 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs778886214 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98961,RMVar_hsa_circ_115171,RMVar_hsa_circ_142084,RMVar_hsa_circ_79404,RMVar_hsa_circ_142085,RMVar_hsa_circ_142083 38427 RMVar_ID_38427 Human_SNP_ID_422050115 A-to-I Human chr10 + 12074565 12074565 12074565 TTTTTTTAGTAGAGATGGGGTTTCACCGTGTTAGCCAGGATGGTTTCGATCTCTTGACCTCATGA TTTTTTTAGTAGAGATGGGGTTTCACCGTGTTGGCCAGGATGGTTTCGATCTCTTGACCTCATGA A G DHTKD1 Ensembl:ENSG00000181192 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs778886214 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98961,RMVar_hsa_circ_115171,RMVar_hsa_circ_142084,RMVar_hsa_circ_79404,RMVar_hsa_circ_142085,RMVar_hsa_circ_142083 38428 RMVar_ID_38428 Human_SNP_ID_422050993 A-to-I Human chr10 + 12077340 12077337 12077340 ACCTCTGCCTCCTGGGTTCAAGCAATTCTCCTACTTCATCTTCCTGAGTAGCTGGGATTACAGGT ACCTCTGCCTCCTGGGTTCAAGCAATTCTC___CTTCATCTTCCTGAGTAGCTGGGATTACAGGT CCTA C DHTKD1 Ensembl:ENSG00000181192 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1360411399 Functional Loss DEL dbSNP153 31..33 33 - - - RMVar_hsa_circ_98961,RMVar_hsa_circ_115171,RMVar_hsa_circ_142084,RMVar_hsa_circ_79404,RMVar_hsa_circ_142085,RMVar_hsa_circ_142083 38429 RMVar_ID_38429 Human_SNP_ID_422050995 A-to-I Human chr10 + 12077340 12077340 12077340 ACCTCTGCCTCCTGGGTTCAAGCAATTCTCCTACTTCATCTTCCTGAGTAGCTGGGATTACAGGT ACCTCTGCCTCCTGGGTTCAAGCAATTCTCCTCCTTCATCTTCCTGAGTAGCTGGGATTACAGGT A C DHTKD1 Ensembl:ENSG00000181192 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs978517307 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98961,RMVar_hsa_circ_115171,RMVar_hsa_circ_142084,RMVar_hsa_circ_79404,RMVar_hsa_circ_142085,RMVar_hsa_circ_142083 38430 RMVar_ID_38430 Human_SNP_ID_422053221 A-to-I Human chr10 + 12084930 12084930 12084930 AAAATTAGCCAGGCATGCTGGTGCATGCCTGTAATCCTAGCTACTCATGAGGCTGAGGCAGCAGA AAAATTAGCCAGGCATGCTGGTGCATGCCTGTCATCCTAGCTACTCATGAGGCTGAGGCAGCAGA A C DHTKD1 Ensembl:ENSG00000181192 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1313963938 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_142089,RMVar_hsa_circ_290043,RMVar_hsa_circ_98961,RMVar_hsa_circ_115171,RMVar_hsa_circ_312366,RMVar_hsa_circ_142084,RMVar_hsa_circ_79404,RMVar_hsa_circ_142085,RMVar_hsa_circ_142083,RMVar_hsa_circ_318897,RMVar_hsa_circ_301931,RMVar_hsa_circ_305860,RMVar_hsa_circ_296377,RMVar_hsa_circ_281010,RMVar_hsa_circ_285827,RMVar_hsa_circ_282118,RMVar_hsa_circ_272622,RMVar_hsa_circ_279546,RMVar_hsa_circ_272353,RMVar_hsa_circ_142093,RMVar_hsa_circ_142095,RMVar_hsa_circ_142097,RMVar_hsa_circ_142096,RMVar_hsa_circ_142094,RMVar_hsa_circ_142091,RMVar_hsa_circ_142092,RMVar_hsa_circ_142090,RMVar_hsa_circ_27430,RMVar_hsa_circ_311381,RMVar_hsa_circ_142087,RMVar_hsa_circ_142088,RMVar_hsa_circ_361771,RMVar_hsa_circ_142086,RMVar_hsa_circ_358743,RMVar_hsa_circ_316042,RMVar_hsa_circ_326608,RMVar_hsa_circ_315151,RMVar_hsa_circ_288760,RMVar_hsa_circ_293444,RMVar_hsa_circ_286084,RMVar_hsa_circ_142100,RMVar_hsa_circ_142102,RMVar_hsa_circ_142104,RMVar_hsa_circ_142105,RMVar_hsa_circ_142103,RMVar_hsa_circ_142101 38431 RMVar_ID_38431 Human_SNP_ID_422053231 A-to-I Human chr10 + 12084983 12084983 12084983 TGAGGCAGCAGAATTGCTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCCGAGATTGCGCCATTGC TGAGGCAGCAGAATTGCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCCGAGATTGCGCCATTGC A G DHTKD1 Ensembl:ENSG00000181192 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs958573575 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_142089,RMVar_hsa_circ_290043,RMVar_hsa_circ_98961,RMVar_hsa_circ_115171,RMVar_hsa_circ_312366,RMVar_hsa_circ_142084,RMVar_hsa_circ_79404,RMVar_hsa_circ_142085,RMVar_hsa_circ_142083,RMVar_hsa_circ_318897,RMVar_hsa_circ_301931,RMVar_hsa_circ_305860,RMVar_hsa_circ_296377,RMVar_hsa_circ_281010,RMVar_hsa_circ_285827,RMVar_hsa_circ_282118,RMVar_hsa_circ_272622,RMVar_hsa_circ_279546,RMVar_hsa_circ_272353,RMVar_hsa_circ_142093,RMVar_hsa_circ_142095,RMVar_hsa_circ_142097,RMVar_hsa_circ_142096,RMVar_hsa_circ_142094,RMVar_hsa_circ_142091,RMVar_hsa_circ_142092,RMVar_hsa_circ_142090,RMVar_hsa_circ_27430,RMVar_hsa_circ_311381,RMVar_hsa_circ_142087,RMVar_hsa_circ_142088,RMVar_hsa_circ_361771,RMVar_hsa_circ_142086,RMVar_hsa_circ_358743,RMVar_hsa_circ_316042,RMVar_hsa_circ_326608,RMVar_hsa_circ_315151,RMVar_hsa_circ_288760,RMVar_hsa_circ_293444,RMVar_hsa_circ_286084,RMVar_hsa_circ_142100,RMVar_hsa_circ_142102,RMVar_hsa_circ_142104,RMVar_hsa_circ_142105,RMVar_hsa_circ_142103,RMVar_hsa_circ_142101 38432 RMVar_ID_38432 Human_SNP_ID_422053273 A-to-I Human chr10 + 12085145 12085145 12085145 TAGCCTGGCTGACATAGAGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCCAGGGGTGATGG TAGCCTGGCTGACATAGAGAAACCCCGTCTCTGCTAAAAATACAAAAATTAGCCAGGGGTGATGG A G DHTKD1 Ensembl:ENSG00000181192 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs537896186 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_142089,RMVar_hsa_circ_290043,RMVar_hsa_circ_98961,RMVar_hsa_circ_115171,RMVar_hsa_circ_312366,RMVar_hsa_circ_142084,RMVar_hsa_circ_79404,RMVar_hsa_circ_142085,RMVar_hsa_circ_142083,RMVar_hsa_circ_318897,RMVar_hsa_circ_301931,RMVar_hsa_circ_305860,RMVar_hsa_circ_296377,RMVar_hsa_circ_281010,RMVar_hsa_circ_285827,RMVar_hsa_circ_282118,RMVar_hsa_circ_272622,RMVar_hsa_circ_279546,RMVar_hsa_circ_272353,RMVar_hsa_circ_142093,RMVar_hsa_circ_142095,RMVar_hsa_circ_142097,RMVar_hsa_circ_142096,RMVar_hsa_circ_142094,RMVar_hsa_circ_142091,RMVar_hsa_circ_142092,RMVar_hsa_circ_142090,RMVar_hsa_circ_27430,RMVar_hsa_circ_311381,RMVar_hsa_circ_142087,RMVar_hsa_circ_142088,RMVar_hsa_circ_361771,RMVar_hsa_circ_142086,RMVar_hsa_circ_358743,RMVar_hsa_circ_316042,RMVar_hsa_circ_326608,RMVar_hsa_circ_315151,RMVar_hsa_circ_288760,RMVar_hsa_circ_293444,RMVar_hsa_circ_286084,RMVar_hsa_circ_142100,RMVar_hsa_circ_142102,RMVar_hsa_circ_142104,RMVar_hsa_circ_142105,RMVar_hsa_circ_142103,RMVar_hsa_circ_142101 38433 RMVar_ID_38433 Human_SNP_ID_422053446 A-to-I Human chr10 + 12085692 12085692 12085692 CTTGAGGTCAGGAGTTTGATACCAGCCAGGCCAACATGGTGAAACCCCGTGTCTACTAAAAAAAC CTTGAGGTCAGGAGTTTGATACCAGCCAGGCCGACATGGTGAAACCCCGTGTCTACTAAAAAAAC A G DHTKD1 Ensembl:ENSG00000181192 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1234147414 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_142089,RMVar_hsa_circ_290043,RMVar_hsa_circ_98961,RMVar_hsa_circ_115171,RMVar_hsa_circ_312366,RMVar_hsa_circ_142084,RMVar_hsa_circ_79404,RMVar_hsa_circ_142085,RMVar_hsa_circ_142083,RMVar_hsa_circ_318897,RMVar_hsa_circ_301931,RMVar_hsa_circ_305860,RMVar_hsa_circ_296377,RMVar_hsa_circ_281010,RMVar_hsa_circ_285827,RMVar_hsa_circ_282118,RMVar_hsa_circ_272622,RMVar_hsa_circ_279546,RMVar_hsa_circ_272353,RMVar_hsa_circ_142093,RMVar_hsa_circ_142095,RMVar_hsa_circ_142097,RMVar_hsa_circ_142096,RMVar_hsa_circ_142094,RMVar_hsa_circ_142091,RMVar_hsa_circ_142092,RMVar_hsa_circ_142090,RMVar_hsa_circ_27430,RMVar_hsa_circ_311381,RMVar_hsa_circ_142087,RMVar_hsa_circ_142088,RMVar_hsa_circ_361771,RMVar_hsa_circ_142086,RMVar_hsa_circ_358743,RMVar_hsa_circ_316042,RMVar_hsa_circ_326608,RMVar_hsa_circ_315151,RMVar_hsa_circ_288760,RMVar_hsa_circ_293444,RMVar_hsa_circ_286084,RMVar_hsa_circ_142100,RMVar_hsa_circ_142102,RMVar_hsa_circ_142104,RMVar_hsa_circ_142105,RMVar_hsa_circ_142103,RMVar_hsa_circ_142101 38434 RMVar_ID_38434 Human_SNP_ID_422053474 A-to-I Human chr10 + 12085812 12085812 12085812 GGGAAGCTGAGGCAGGAGAATCTCTTGAACCCAGGAGGCGGAGGTTGCAGCGAGCCGAGATCACA GGGAAGCTGAGGCAGGAGAATCTCTTGAACCCGGGAGGCGGAGGTTGCAGCGAGCCGAGATCACA A G DHTKD1 Ensembl:ENSG00000181192 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1465491092 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_142089,RMVar_hsa_circ_290043,RMVar_hsa_circ_98961,RMVar_hsa_circ_115171,RMVar_hsa_circ_312366,RMVar_hsa_circ_142084,RMVar_hsa_circ_79404,RMVar_hsa_circ_142085,RMVar_hsa_circ_142083,RMVar_hsa_circ_318897,RMVar_hsa_circ_301931,RMVar_hsa_circ_305860,RMVar_hsa_circ_296377,RMVar_hsa_circ_281010,RMVar_hsa_circ_285827,RMVar_hsa_circ_282118,RMVar_hsa_circ_272622,RMVar_hsa_circ_279546,RMVar_hsa_circ_272353,RMVar_hsa_circ_142093,RMVar_hsa_circ_142095,RMVar_hsa_circ_142097,RMVar_hsa_circ_142096,RMVar_hsa_circ_142094,RMVar_hsa_circ_142091,RMVar_hsa_circ_142092,RMVar_hsa_circ_142090,RMVar_hsa_circ_27430,RMVar_hsa_circ_311381,RMVar_hsa_circ_142087,RMVar_hsa_circ_142088,RMVar_hsa_circ_361771,RMVar_hsa_circ_142086,RMVar_hsa_circ_358743,RMVar_hsa_circ_316042,RMVar_hsa_circ_326608,RMVar_hsa_circ_315151,RMVar_hsa_circ_288760,RMVar_hsa_circ_293444,RMVar_hsa_circ_286084,RMVar_hsa_circ_142100,RMVar_hsa_circ_142102,RMVar_hsa_circ_142104,RMVar_hsa_circ_142105,RMVar_hsa_circ_142103,RMVar_hsa_circ_142101 38435 RMVar_ID_38435 Human_SNP_ID_422053676 A-to-I Human chr10 + 12086405 12086404 12086405 ATGATGCCTGGCTAATTTTTTGTATTTTTAGTAGAACGGGGTTTCACTGTGTTAGTCAGGATGGT ATGATGCCTGGCTAATTTTTTGTATTTTTAGT_GAACGGGGTTTCACTGTGTTAGTCAGGATGGT TA T DHTKD1 Ensembl:ENSG00000181192 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1439563638 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_142089,RMVar_hsa_circ_290043,RMVar_hsa_circ_98961,RMVar_hsa_circ_115171,RMVar_hsa_circ_312366,RMVar_hsa_circ_142084,RMVar_hsa_circ_79404,RMVar_hsa_circ_142085,RMVar_hsa_circ_142083,RMVar_hsa_circ_318897,RMVar_hsa_circ_301931,RMVar_hsa_circ_305860,RMVar_hsa_circ_296377,RMVar_hsa_circ_281010,RMVar_hsa_circ_285827,RMVar_hsa_circ_282118,RMVar_hsa_circ_272622,RMVar_hsa_circ_279546,RMVar_hsa_circ_272353,RMVar_hsa_circ_142093,RMVar_hsa_circ_142095,RMVar_hsa_circ_142097,RMVar_hsa_circ_142096,RMVar_hsa_circ_142094,RMVar_hsa_circ_142091,RMVar_hsa_circ_142092,RMVar_hsa_circ_142090,RMVar_hsa_circ_27430,RMVar_hsa_circ_311381,RMVar_hsa_circ_142087,RMVar_hsa_circ_142088,RMVar_hsa_circ_361771,RMVar_hsa_circ_142086,RMVar_hsa_circ_358743,RMVar_hsa_circ_316042,RMVar_hsa_circ_326608,RMVar_hsa_circ_315151,RMVar_hsa_circ_288760,RMVar_hsa_circ_293444,RMVar_hsa_circ_286084,RMVar_hsa_circ_142100,RMVar_hsa_circ_142102,RMVar_hsa_circ_142104,RMVar_hsa_circ_142105,RMVar_hsa_circ_142103,RMVar_hsa_circ_142101 38436 RMVar_ID_38436 Human_SNP_ID_422053685 A-to-I Human chr10 + 12086426 12086426 12086426 GTATTTTTAGTAGAACGGGGTTTCACTGTGTTAGTCAGGATGGTCTCGATCTCCTGACCTCGTGA GTATTTTTAGTAGAACGGGGTTTCACTGTGTTTGTCAGGATGGTCTCGATCTCCTGACCTCGTGA A T DHTKD1 Ensembl:ENSG00000181192 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1394076455 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_142089,RMVar_hsa_circ_290043,RMVar_hsa_circ_98961,RMVar_hsa_circ_115171,RMVar_hsa_circ_312366,RMVar_hsa_circ_142084,RMVar_hsa_circ_79404,RMVar_hsa_circ_142085,RMVar_hsa_circ_142083,RMVar_hsa_circ_318897,RMVar_hsa_circ_301931,RMVar_hsa_circ_305860,RMVar_hsa_circ_296377,RMVar_hsa_circ_281010,RMVar_hsa_circ_285827,RMVar_hsa_circ_282118,RMVar_hsa_circ_272622,RMVar_hsa_circ_279546,RMVar_hsa_circ_272353,RMVar_hsa_circ_142093,RMVar_hsa_circ_142095,RMVar_hsa_circ_142097,RMVar_hsa_circ_142096,RMVar_hsa_circ_142094,RMVar_hsa_circ_142091,RMVar_hsa_circ_142092,RMVar_hsa_circ_142090,RMVar_hsa_circ_27430,RMVar_hsa_circ_311381,RMVar_hsa_circ_142087,RMVar_hsa_circ_142088,RMVar_hsa_circ_361771,RMVar_hsa_circ_142086,RMVar_hsa_circ_358743,RMVar_hsa_circ_316042,RMVar_hsa_circ_326608,RMVar_hsa_circ_315151,RMVar_hsa_circ_288760,RMVar_hsa_circ_293444,RMVar_hsa_circ_286084,RMVar_hsa_circ_142100,RMVar_hsa_circ_142102,RMVar_hsa_circ_142104,RMVar_hsa_circ_142105,RMVar_hsa_circ_142103,RMVar_hsa_circ_142101 38437 RMVar_ID_38437 Human_SNP_ID_422053821 A-to-I Human chr10 + 12086961 12086961 12086961 CACCTGCCTTGGCCTCCCGAAGTGCTGGGATTACAGACGTGAACCACCATGCCTGGCCTGGTCTT CACCTGCCTTGGCCTCCCGAAGTGCTGGGATTGCAGACGTGAACCACCATGCCTGGCCTGGTCTT A G DHTKD1 Ensembl:ENSG00000181192 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs937818019 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_142089,RMVar_hsa_circ_290043,RMVar_hsa_circ_98961,RMVar_hsa_circ_115171,RMVar_hsa_circ_312366,RMVar_hsa_circ_142084,RMVar_hsa_circ_79404,RMVar_hsa_circ_142085,RMVar_hsa_circ_142083,RMVar_hsa_circ_318897,RMVar_hsa_circ_301931,RMVar_hsa_circ_305860,RMVar_hsa_circ_296377,RMVar_hsa_circ_281010,RMVar_hsa_circ_285827,RMVar_hsa_circ_282118,RMVar_hsa_circ_272622,RMVar_hsa_circ_279546,RMVar_hsa_circ_272353,RMVar_hsa_circ_142093,RMVar_hsa_circ_142095,RMVar_hsa_circ_142097,RMVar_hsa_circ_142096,RMVar_hsa_circ_142094,RMVar_hsa_circ_142091,RMVar_hsa_circ_142092,RMVar_hsa_circ_142090,RMVar_hsa_circ_27430,RMVar_hsa_circ_311381,RMVar_hsa_circ_142087,RMVar_hsa_circ_142088,RMVar_hsa_circ_361771,RMVar_hsa_circ_142086,RMVar_hsa_circ_358743,RMVar_hsa_circ_316042,RMVar_hsa_circ_326608,RMVar_hsa_circ_315151,RMVar_hsa_circ_288760,RMVar_hsa_circ_293444,RMVar_hsa_circ_286084,RMVar_hsa_circ_142100,RMVar_hsa_circ_142102,RMVar_hsa_circ_142104,RMVar_hsa_circ_142105,RMVar_hsa_circ_142103,RMVar_hsa_circ_142101 38438 RMVar_ID_38438 Human_SNP_ID_422055429 A-to-I Human chr10 + 12092184 12092184 12092184 TTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCAGGCTGGTCTTGAACTCCTGACCTC TTTTGTATTTTTAGTAGAGACGGGGTTTCACCGTGTTGGCAGGCTGGTCTTGAACTCCTGACCTC A G DHTKD1 Ensembl:ENSG00000181192 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1367280854 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_142089,RMVar_hsa_circ_290043,RMVar_hsa_circ_115171,RMVar_hsa_circ_312366,RMVar_hsa_circ_142084,RMVar_hsa_circ_79404,RMVar_hsa_circ_142085,RMVar_hsa_circ_318897,RMVar_hsa_circ_301931,RMVar_hsa_circ_296377,RMVar_hsa_circ_281010,RMVar_hsa_circ_282118,RMVar_hsa_circ_272622,RMVar_hsa_circ_272353,RMVar_hsa_circ_142093,RMVar_hsa_circ_142094,RMVar_hsa_circ_142091,RMVar_hsa_circ_142092,RMVar_hsa_circ_142090,RMVar_hsa_circ_8032,RMVar_hsa_circ_27430,RMVar_hsa_circ_311381,RMVar_hsa_circ_142087,RMVar_hsa_circ_142088,RMVar_hsa_circ_361771,RMVar_hsa_circ_142086,RMVar_hsa_circ_358743,RMVar_hsa_circ_316042,RMVar_hsa_circ_288760,RMVar_hsa_circ_286084,RMVar_hsa_circ_142100,RMVar_hsa_circ_142102,RMVar_hsa_circ_142101,RMVar_hsa_circ_266206,RMVar_hsa_circ_348291,RMVar_hsa_circ_337314,RMVar_hsa_circ_290574,RMVar_hsa_circ_118851,RMVar_hsa_circ_18463,RMVar_hsa_circ_32065,RMVar_hsa_circ_295494,RMVar_hsa_circ_142108,RMVar_hsa_circ_142109,RMVar_hsa_circ_142107,RMVar_hsa_circ_352213,RMVar_hsa_circ_373470,RMVar_hsa_circ_271703,RMVar_hsa_circ_66717,RMVar_hsa_circ_142112,RMVar_hsa_circ_142114,RMVar_hsa_circ_142115,RMVar_hsa_circ_142113,RMVar_hsa_circ_334485,RMVar_hsa_circ_342289,RMVar_hsa_circ_367073,RMVar_hsa_circ_125090,RMVar_hsa_circ_142116,RMVar_hsa_circ_93028,RMVar_hsa_circ_115817,RMVar_hsa_circ_142118,RMVar_hsa_circ_142117,RMVar_hsa_circ_142121,RMVar_hsa_circ_142120 38439 RMVar_ID_38439 Human_SNP_ID_422057541 A-to-I Human chr10 + 12099979 12099979 12099979 CACCAGGCCTAGCTAATTTTTGTATTTTTAGTAGAGATGGAGTTTCACCATGTTGTCCAGGCTGG CACCAGGCCTAGCTAATTTTTGTATTTTTAGTGGAGATGGAGTTTCACCATGTTGTCCAGGCTGG A G DHTKD1 Ensembl:ENSG00000181192 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1472501443 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13286,RMVar_hsa_circ_142089,RMVar_hsa_circ_290043,RMVar_hsa_circ_312366,RMVar_hsa_circ_79404,RMVar_hsa_circ_142085,RMVar_hsa_circ_318897,RMVar_hsa_circ_301931,RMVar_hsa_circ_281010,RMVar_hsa_circ_282118,RMVar_hsa_circ_272622,RMVar_hsa_circ_142091,RMVar_hsa_circ_142092,RMVar_hsa_circ_142090,RMVar_hsa_circ_8032,RMVar_hsa_circ_27430,RMVar_hsa_circ_142087,RMVar_hsa_circ_142088,RMVar_hsa_circ_361771,RMVar_hsa_circ_142086,RMVar_hsa_circ_358743,RMVar_hsa_circ_316042,RMVar_hsa_circ_288760,RMVar_hsa_circ_142100,RMVar_hsa_circ_142101,RMVar_hsa_circ_266206,RMVar_hsa_circ_348291,RMVar_hsa_circ_290574,RMVar_hsa_circ_118851,RMVar_hsa_circ_18463,RMVar_hsa_circ_32065,RMVar_hsa_circ_295494,RMVar_hsa_circ_142108,RMVar_hsa_circ_142109,RMVar_hsa_circ_352213,RMVar_hsa_circ_373470,RMVar_hsa_circ_66717,RMVar_hsa_circ_142114,RMVar_hsa_circ_142115,RMVar_hsa_circ_142113,RMVar_hsa_circ_342289,RMVar_hsa_circ_367073,RMVar_hsa_circ_125090,RMVar_hsa_circ_70661,RMVar_hsa_circ_142116,RMVar_hsa_circ_93028,RMVar_hsa_circ_115817,RMVar_hsa_circ_142118,RMVar_hsa_circ_142117,RMVar_hsa_circ_335717,RMVar_hsa_circ_142121,RMVar_hsa_circ_142120,RMVar_hsa_circ_342137,RMVar_hsa_circ_342553,RMVar_hsa_circ_273375,RMVar_hsa_circ_117945,RMVar_hsa_circ_142123,RMVar_hsa_circ_142125,RMVar_hsa_circ_142126,RMVar_hsa_circ_142124,RMVar_hsa_circ_329929,RMVar_hsa_circ_357999,RMVar_hsa_circ_99155,RMVar_hsa_circ_104834,RMVar_hsa_circ_20246,RMVar_hsa_circ_142128,RMVar_hsa_circ_142130,RMVar_hsa_circ_142129,RMVar_hsa_circ_142127 38440 RMVar_ID_38440 Human_SNP_ID_422058468 A-to-I Human chr10 + 12103129 12103129 12103129 CCTGTAATCCCAGCTACTCAGGAGGTTGAGGCAGGAGAATTGCTTGAACCCAGGAGGCAGAGGTA CCTGTAATCCCAGCTACTCAGGAGGTTGAGGCGGGAGAATTGCTTGAACCCAGGAGGCAGAGGTA A G DHTKD1 Ensembl:ENSG00000181192 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs977557479 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13286,RMVar_hsa_circ_142089,RMVar_hsa_circ_312366,RMVar_hsa_circ_79404,RMVar_hsa_circ_142085,RMVar_hsa_circ_318897,RMVar_hsa_circ_301931,RMVar_hsa_circ_282118,RMVar_hsa_circ_272622,RMVar_hsa_circ_142090,RMVar_hsa_circ_8032,RMVar_hsa_circ_142087,RMVar_hsa_circ_142088,RMVar_hsa_circ_361771,RMVar_hsa_circ_142086,RMVar_hsa_circ_358743,RMVar_hsa_circ_316042,RMVar_hsa_circ_142100,RMVar_hsa_circ_266206,RMVar_hsa_circ_290574,RMVar_hsa_circ_118851,RMVar_hsa_circ_18463,RMVar_hsa_circ_32065,RMVar_hsa_circ_142108,RMVar_hsa_circ_142109,RMVar_hsa_circ_373470,RMVar_hsa_circ_66717,RMVar_hsa_circ_142114,RMVar_hsa_circ_142115,RMVar_hsa_circ_367073,RMVar_hsa_circ_125090,RMVar_hsa_circ_70661,RMVar_hsa_circ_142116,RMVar_hsa_circ_93028,RMVar_hsa_circ_115817,RMVar_hsa_circ_142118,RMVar_hsa_circ_142117,RMVar_hsa_circ_335717,RMVar_hsa_circ_142121,RMVar_hsa_circ_142120,RMVar_hsa_circ_342553,RMVar_hsa_circ_273375,RMVar_hsa_circ_117945,RMVar_hsa_circ_142125,RMVar_hsa_circ_142126,RMVar_hsa_circ_142124,RMVar_hsa_circ_329929,RMVar_hsa_circ_357999,RMVar_hsa_circ_99155,RMVar_hsa_circ_104834,RMVar_hsa_circ_324932,RMVar_hsa_circ_142128,RMVar_hsa_circ_142130,RMVar_hsa_circ_142129,RMVar_hsa_circ_142127,RMVar_hsa_circ_372622,RMVar_hsa_circ_285912,RMVar_hsa_circ_287548,RMVar_hsa_circ_142134,RMVar_hsa_circ_142133,RMVar_hsa_circ_113041,RMVar_hsa_circ_327818 38441 RMVar_ID_38441 Human_SNP_ID_422058799 A-to-I Human chr10 + 12104344 12104344 12104344 GGGACTGCAGGTGTGCGCCACCAGGCCCTGCTAATTTTTGAATTTGTAGCAGAGACAGGGTCTCG GGGACTGCAGGTGTGCGCCACCAGGCCCTGCTGATTTTTGAATTTGTAGCAGAGACAGGGTCTCG A G DHTKD1 Ensembl:ENSG00000181192 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1018875693 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13286,RMVar_hsa_circ_142089,RMVar_hsa_circ_312366,RMVar_hsa_circ_79404,RMVar_hsa_circ_142085,RMVar_hsa_circ_318897,RMVar_hsa_circ_301931,RMVar_hsa_circ_282118,RMVar_hsa_circ_272622,RMVar_hsa_circ_142090,RMVar_hsa_circ_8032,RMVar_hsa_circ_142087,RMVar_hsa_circ_142088,RMVar_hsa_circ_361771,RMVar_hsa_circ_142086,RMVar_hsa_circ_358743,RMVar_hsa_circ_316042,RMVar_hsa_circ_142100,RMVar_hsa_circ_266206,RMVar_hsa_circ_290574,RMVar_hsa_circ_118851,RMVar_hsa_circ_18463,RMVar_hsa_circ_32065,RMVar_hsa_circ_142108,RMVar_hsa_circ_142109,RMVar_hsa_circ_373470,RMVar_hsa_circ_66717,RMVar_hsa_circ_142114,RMVar_hsa_circ_142115,RMVar_hsa_circ_367073,RMVar_hsa_circ_125090,RMVar_hsa_circ_70661,RMVar_hsa_circ_142116,RMVar_hsa_circ_93028,RMVar_hsa_circ_115817,RMVar_hsa_circ_142118,RMVar_hsa_circ_142117,RMVar_hsa_circ_335717,RMVar_hsa_circ_142121,RMVar_hsa_circ_142120,RMVar_hsa_circ_342553,RMVar_hsa_circ_273375,RMVar_hsa_circ_117945,RMVar_hsa_circ_142125,RMVar_hsa_circ_142126,RMVar_hsa_circ_142124,RMVar_hsa_circ_329929,RMVar_hsa_circ_357999,RMVar_hsa_circ_99155,RMVar_hsa_circ_104834,RMVar_hsa_circ_324932,RMVar_hsa_circ_142128,RMVar_hsa_circ_142130,RMVar_hsa_circ_142129,RMVar_hsa_circ_142127,RMVar_hsa_circ_372622,RMVar_hsa_circ_285912,RMVar_hsa_circ_287548,RMVar_hsa_circ_142134,RMVar_hsa_circ_142133,RMVar_hsa_circ_113041,RMVar_hsa_circ_327818 38442 RMVar_ID_38442 Human_SNP_ID_422058800 A-to-I Human chr10 + 12104344 12104344 12104344 GGGACTGCAGGTGTGCGCCACCAGGCCCTGCTAATTTTTGAATTTGTAGCAGAGACAGGGTCTCG GGGACTGCAGGTGTGCGCCACCAGGCCCTGCTTATTTTTGAATTTGTAGCAGAGACAGGGTCTCG A T DHTKD1 Ensembl:ENSG00000181192 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1018875693 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13286,RMVar_hsa_circ_142089,RMVar_hsa_circ_312366,RMVar_hsa_circ_79404,RMVar_hsa_circ_142085,RMVar_hsa_circ_318897,RMVar_hsa_circ_301931,RMVar_hsa_circ_282118,RMVar_hsa_circ_272622,RMVar_hsa_circ_142090,RMVar_hsa_circ_8032,RMVar_hsa_circ_142087,RMVar_hsa_circ_142088,RMVar_hsa_circ_361771,RMVar_hsa_circ_142086,RMVar_hsa_circ_358743,RMVar_hsa_circ_316042,RMVar_hsa_circ_142100,RMVar_hsa_circ_266206,RMVar_hsa_circ_290574,RMVar_hsa_circ_118851,RMVar_hsa_circ_18463,RMVar_hsa_circ_32065,RMVar_hsa_circ_142108,RMVar_hsa_circ_142109,RMVar_hsa_circ_373470,RMVar_hsa_circ_66717,RMVar_hsa_circ_142114,RMVar_hsa_circ_142115,RMVar_hsa_circ_367073,RMVar_hsa_circ_125090,RMVar_hsa_circ_70661,RMVar_hsa_circ_142116,RMVar_hsa_circ_93028,RMVar_hsa_circ_115817,RMVar_hsa_circ_142118,RMVar_hsa_circ_142117,RMVar_hsa_circ_335717,RMVar_hsa_circ_142121,RMVar_hsa_circ_142120,RMVar_hsa_circ_342553,RMVar_hsa_circ_273375,RMVar_hsa_circ_117945,RMVar_hsa_circ_142125,RMVar_hsa_circ_142126,RMVar_hsa_circ_142124,RMVar_hsa_circ_329929,RMVar_hsa_circ_357999,RMVar_hsa_circ_99155,RMVar_hsa_circ_104834,RMVar_hsa_circ_324932,RMVar_hsa_circ_142128,RMVar_hsa_circ_142130,RMVar_hsa_circ_142129,RMVar_hsa_circ_142127,RMVar_hsa_circ_372622,RMVar_hsa_circ_285912,RMVar_hsa_circ_287548,RMVar_hsa_circ_142134,RMVar_hsa_circ_142133,RMVar_hsa_circ_113041,RMVar_hsa_circ_327818 38443 RMVar_ID_38443 Human_SNP_ID_422060155 A-to-I Human chr10 + 12109461 12109461 12109461 GAGTAGGTGGGGGATACAGTTTCGGAGTCATCAGCCACTAGATGACATTGACAGTCATGAGTCTG GAGTAGGTGGGGGATACAGTTTCGGAGTCATCGGCCACTAGATGACATTGACAGTCATGAGTCTG A G DHTKD1 Ensembl:ENSG00000181192 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7897732 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13286,RMVar_hsa_circ_312366,RMVar_hsa_circ_282118,RMVar_hsa_circ_272622,RMVar_hsa_circ_142087,RMVar_hsa_circ_142088,RMVar_hsa_circ_142086,RMVar_hsa_circ_358743,RMVar_hsa_circ_316042,RMVar_hsa_circ_142100,RMVar_hsa_circ_266206,RMVar_hsa_circ_290574,RMVar_hsa_circ_118851,RMVar_hsa_circ_142108,RMVar_hsa_circ_142109,RMVar_hsa_circ_373470,RMVar_hsa_circ_66717,RMVar_hsa_circ_142114,RMVar_hsa_circ_142115,RMVar_hsa_circ_367073,RMVar_hsa_circ_70661,RMVar_hsa_circ_142116,RMVar_hsa_circ_93028,RMVar_hsa_circ_115817,RMVar_hsa_circ_142117,RMVar_hsa_circ_335717,RMVar_hsa_circ_142121,RMVar_hsa_circ_142120,RMVar_hsa_circ_273375,RMVar_hsa_circ_142125,RMVar_hsa_circ_142126,RMVar_hsa_circ_357999,RMVar_hsa_circ_99155,RMVar_hsa_circ_104834,RMVar_hsa_circ_56050,RMVar_hsa_circ_324932,RMVar_hsa_circ_142128,RMVar_hsa_circ_142129,RMVar_hsa_circ_142127,RMVar_hsa_circ_372622,RMVar_hsa_circ_287548,RMVar_hsa_circ_142134,RMVar_hsa_circ_142133,RMVar_hsa_circ_113041,RMVar_hsa_circ_316140,RMVar_hsa_circ_360566,RMVar_hsa_circ_142139,RMVar_hsa_circ_96317,RMVar_hsa_circ_142136,RMVar_hsa_circ_142137,RMVar_hsa_circ_350651,RMVar_hsa_circ_316822,RMVar_hsa_circ_66117,RMVar_hsa_circ_142138 38444 RMVar_ID_38444 Human_SNP_ID_422060454 A-to-I Human chr10 + 12110897 12110897 12110897 CCATTTCTGCTAAAAATAAAACTAAAAAAATTAGCTGGGTGGGTGGTGGTGCGTGCCCATAATCC CCATTTCTGCTAAAAATAAAACTAAAAAAATTGGCTGGGTGGGTGGTGGTGCGTGCCCATAATCC A G DHTKD1 Ensembl:ENSG00000181192 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1024560062 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13286,RMVar_hsa_circ_312366,RMVar_hsa_circ_282118,RMVar_hsa_circ_272622,RMVar_hsa_circ_142087,RMVar_hsa_circ_142088,RMVar_hsa_circ_142086,RMVar_hsa_circ_358743,RMVar_hsa_circ_316042,RMVar_hsa_circ_142100,RMVar_hsa_circ_266206,RMVar_hsa_circ_290574,RMVar_hsa_circ_118851,RMVar_hsa_circ_142108,RMVar_hsa_circ_142109,RMVar_hsa_circ_373470,RMVar_hsa_circ_66717,RMVar_hsa_circ_142114,RMVar_hsa_circ_142115,RMVar_hsa_circ_367073,RMVar_hsa_circ_70661,RMVar_hsa_circ_142116,RMVar_hsa_circ_93028,RMVar_hsa_circ_115817,RMVar_hsa_circ_142117,RMVar_hsa_circ_335717,RMVar_hsa_circ_142121,RMVar_hsa_circ_142120,RMVar_hsa_circ_273375,RMVar_hsa_circ_142125,RMVar_hsa_circ_142126,RMVar_hsa_circ_357999,RMVar_hsa_circ_99155,RMVar_hsa_circ_104834,RMVar_hsa_circ_56050,RMVar_hsa_circ_324932,RMVar_hsa_circ_142128,RMVar_hsa_circ_142129,RMVar_hsa_circ_142127,RMVar_hsa_circ_372622,RMVar_hsa_circ_287548,RMVar_hsa_circ_142134,RMVar_hsa_circ_142133,RMVar_hsa_circ_113041,RMVar_hsa_circ_316140,RMVar_hsa_circ_360566,RMVar_hsa_circ_142139,RMVar_hsa_circ_96317,RMVar_hsa_circ_142136,RMVar_hsa_circ_142137,RMVar_hsa_circ_350651,RMVar_hsa_circ_316822,RMVar_hsa_circ_66117,RMVar_hsa_circ_142138 38445 RMVar_ID_38445 Human_SNP_ID_422060469 A-to-I Human chr10 + 12110961 12110961 12110961 CTCACTACTTGGGAGGCTGAGGTGGGAGGATCACTTGAGCCTGGGAGGCGGAGGTTGTAGTGAGC CTCACTACTTGGGAGGCTGAGGTGGGAGGATCGCTTGAGCCTGGGAGGCGGAGGTTGTAGTGAGC A G DHTKD1 Ensembl:ENSG00000181192 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs533848535 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13286,RMVar_hsa_circ_312366,RMVar_hsa_circ_282118,RMVar_hsa_circ_272622,RMVar_hsa_circ_142087,RMVar_hsa_circ_142088,RMVar_hsa_circ_142086,RMVar_hsa_circ_358743,RMVar_hsa_circ_316042,RMVar_hsa_circ_142100,RMVar_hsa_circ_266206,RMVar_hsa_circ_290574,RMVar_hsa_circ_118851,RMVar_hsa_circ_142108,RMVar_hsa_circ_142109,RMVar_hsa_circ_373470,RMVar_hsa_circ_66717,RMVar_hsa_circ_142114,RMVar_hsa_circ_142115,RMVar_hsa_circ_367073,RMVar_hsa_circ_70661,RMVar_hsa_circ_142116,RMVar_hsa_circ_93028,RMVar_hsa_circ_115817,RMVar_hsa_circ_142117,RMVar_hsa_circ_335717,RMVar_hsa_circ_142121,RMVar_hsa_circ_142120,RMVar_hsa_circ_273375,RMVar_hsa_circ_142125,RMVar_hsa_circ_142126,RMVar_hsa_circ_357999,RMVar_hsa_circ_99155,RMVar_hsa_circ_104834,RMVar_hsa_circ_56050,RMVar_hsa_circ_324932,RMVar_hsa_circ_142128,RMVar_hsa_circ_142129,RMVar_hsa_circ_142127,RMVar_hsa_circ_372622,RMVar_hsa_circ_287548,RMVar_hsa_circ_142134,RMVar_hsa_circ_142133,RMVar_hsa_circ_113041,RMVar_hsa_circ_316140,RMVar_hsa_circ_360566,RMVar_hsa_circ_142139,RMVar_hsa_circ_96317,RMVar_hsa_circ_142136,RMVar_hsa_circ_142137,RMVar_hsa_circ_350651,RMVar_hsa_circ_316822,RMVar_hsa_circ_66117,RMVar_hsa_circ_142138 38446 RMVar_ID_38446 Human_SNP_ID_422060548 A-to-I Human chr10 + 12111205 12111205 12111205 CTTTTATTTTTGTGATGGCGTCTTGCTCTGTCACCCAGGCTGTAGTGCAATGCTGCAGTCTTGGC CTTTTATTTTTGTGATGGCGTCTTGCTCTGTCTCCCAGGCTGTAGTGCAATGCTGCAGTCTTGGC A T DHTKD1 Ensembl:ENSG00000181192 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1052490589 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13286,RMVar_hsa_circ_312366,RMVar_hsa_circ_282118,RMVar_hsa_circ_272622,RMVar_hsa_circ_142087,RMVar_hsa_circ_142088,RMVar_hsa_circ_142086,RMVar_hsa_circ_358743,RMVar_hsa_circ_316042,RMVar_hsa_circ_142100,RMVar_hsa_circ_266206,RMVar_hsa_circ_290574,RMVar_hsa_circ_118851,RMVar_hsa_circ_142108,RMVar_hsa_circ_142109,RMVar_hsa_circ_373470,RMVar_hsa_circ_66717,RMVar_hsa_circ_142114,RMVar_hsa_circ_142115,RMVar_hsa_circ_367073,RMVar_hsa_circ_70661,RMVar_hsa_circ_142116,RMVar_hsa_circ_93028,RMVar_hsa_circ_115817,RMVar_hsa_circ_142117,RMVar_hsa_circ_335717,RMVar_hsa_circ_142121,RMVar_hsa_circ_142120,RMVar_hsa_circ_273375,RMVar_hsa_circ_142125,RMVar_hsa_circ_142126,RMVar_hsa_circ_357999,RMVar_hsa_circ_99155,RMVar_hsa_circ_104834,RMVar_hsa_circ_56050,RMVar_hsa_circ_324932,RMVar_hsa_circ_142128,RMVar_hsa_circ_142129,RMVar_hsa_circ_142127,RMVar_hsa_circ_372622,RMVar_hsa_circ_287548,RMVar_hsa_circ_142134,RMVar_hsa_circ_142133,RMVar_hsa_circ_113041,RMVar_hsa_circ_316140,RMVar_hsa_circ_360566,RMVar_hsa_circ_142139,RMVar_hsa_circ_96317,RMVar_hsa_circ_142136,RMVar_hsa_circ_142137,RMVar_hsa_circ_350651,RMVar_hsa_circ_316822,RMVar_hsa_circ_66117,RMVar_hsa_circ_142138 38447 RMVar_ID_38447 Human_SNP_ID_422061104 A-to-I Human chr10 + 12113253 12113253 12113253 GCAGTCTTGCTCTGTCGCCCAGGCTGGAGTGCAATGGTGCAATCTCGGCCCGTTGCAACCTCTGA GCAGTCTTGCTCTGTCGCCCAGGCTGGAGTGCGATGGTGCAATCTCGGCCCGTTGCAACCTCTGA A G DHTKD1 Ensembl:ENSG00000181192 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs770017409 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_312366,RMVar_hsa_circ_282118,RMVar_hsa_circ_142087,RMVar_hsa_circ_142086,RMVar_hsa_circ_316042,RMVar_hsa_circ_142100,RMVar_hsa_circ_266206,RMVar_hsa_circ_290574,RMVar_hsa_circ_142109,RMVar_hsa_circ_66717,RMVar_hsa_circ_142115,RMVar_hsa_circ_367073,RMVar_hsa_circ_70661,RMVar_hsa_circ_142116,RMVar_hsa_circ_93028,RMVar_hsa_circ_115817,RMVar_hsa_circ_142117,RMVar_hsa_circ_142121,RMVar_hsa_circ_142120,RMVar_hsa_circ_273375,RMVar_hsa_circ_142126,RMVar_hsa_circ_357999,RMVar_hsa_circ_99155,RMVar_hsa_circ_104834,RMVar_hsa_circ_56050,RMVar_hsa_circ_324932,RMVar_hsa_circ_142128,RMVar_hsa_circ_142129,RMVar_hsa_circ_142127,RMVar_hsa_circ_287548,RMVar_hsa_circ_360566,RMVar_hsa_circ_142139,RMVar_hsa_circ_96317,RMVar_hsa_circ_142137,RMVar_hsa_circ_316822,RMVar_hsa_circ_66117,RMVar_hsa_circ_142141,RMVar_hsa_circ_281640,RMVar_hsa_circ_309759,RMVar_hsa_circ_142140 38448 RMVar_ID_38448 Human_SNP_ID_422061152 A-to-I Human chr10 + 12113412 12113412 12113412 TAGAGATGGGGTTTCGCCATCTTGGCCAGACTAGTCTCTAACTCTTGACCTCAGGTGATTCGCCC TAGAGATGGGGTTTCGCCATCTTGGCCAGACTGGTCTCTAACTCTTGACCTCAGGTGATTCGCCC A G DHTKD1 Ensembl:ENSG00000181192 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1480656294 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_312366,RMVar_hsa_circ_282118,RMVar_hsa_circ_142087,RMVar_hsa_circ_142086,RMVar_hsa_circ_316042,RMVar_hsa_circ_142100,RMVar_hsa_circ_266206,RMVar_hsa_circ_290574,RMVar_hsa_circ_142109,RMVar_hsa_circ_66717,RMVar_hsa_circ_142115,RMVar_hsa_circ_367073,RMVar_hsa_circ_70661,RMVar_hsa_circ_142116,RMVar_hsa_circ_93028,RMVar_hsa_circ_115817,RMVar_hsa_circ_142117,RMVar_hsa_circ_142121,RMVar_hsa_circ_142120,RMVar_hsa_circ_273375,RMVar_hsa_circ_142126,RMVar_hsa_circ_357999,RMVar_hsa_circ_99155,RMVar_hsa_circ_104834,RMVar_hsa_circ_56050,RMVar_hsa_circ_324932,RMVar_hsa_circ_142128,RMVar_hsa_circ_142129,RMVar_hsa_circ_142127,RMVar_hsa_circ_287548,RMVar_hsa_circ_360566,RMVar_hsa_circ_142139,RMVar_hsa_circ_96317,RMVar_hsa_circ_142137,RMVar_hsa_circ_316822,RMVar_hsa_circ_66117,RMVar_hsa_circ_142141,RMVar_hsa_circ_281640,RMVar_hsa_circ_309759,RMVar_hsa_circ_142140 38449 RMVar_ID_38449 Human_SNP_ID_422061212 A-to-I Human chr10 + 12113668 12113668 12113668 GGCTATTAGGCTGGGCATGGTGGCTCATGCCTATAATTCCAGGACTTTGGGAGGCCTAGGCAAGA GGCTATTAGGCTGGGCATGGTGGCTCATGCCTGTAATTCCAGGACTTTGGGAGGCCTAGGCAAGA A G DHTKD1 Ensembl:ENSG00000181192 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs184159027 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_312366,RMVar_hsa_circ_282118,RMVar_hsa_circ_142087,RMVar_hsa_circ_142086,RMVar_hsa_circ_316042,RMVar_hsa_circ_142100,RMVar_hsa_circ_266206,RMVar_hsa_circ_290574,RMVar_hsa_circ_142109,RMVar_hsa_circ_66717,RMVar_hsa_circ_142115,RMVar_hsa_circ_367073,RMVar_hsa_circ_70661,RMVar_hsa_circ_142116,RMVar_hsa_circ_93028,RMVar_hsa_circ_115817,RMVar_hsa_circ_142117,RMVar_hsa_circ_142121,RMVar_hsa_circ_142120,RMVar_hsa_circ_273375,RMVar_hsa_circ_142126,RMVar_hsa_circ_357999,RMVar_hsa_circ_99155,RMVar_hsa_circ_104834,RMVar_hsa_circ_56050,RMVar_hsa_circ_324932,RMVar_hsa_circ_142128,RMVar_hsa_circ_142129,RMVar_hsa_circ_142127,RMVar_hsa_circ_287548,RMVar_hsa_circ_360566,RMVar_hsa_circ_142139,RMVar_hsa_circ_96317,RMVar_hsa_circ_142137,RMVar_hsa_circ_316822,RMVar_hsa_circ_66117,RMVar_hsa_circ_142141,RMVar_hsa_circ_281640,RMVar_hsa_circ_309759,RMVar_hsa_circ_142140 38450 RMVar_ID_38450 Human_SNP_ID_422061972 A-to-I Human chr10 + 12116446 12116446 12116446 GATGGAGTTTCCTGTTACCCAGGCTATAGTGCAATGGTGTGATCTCAGCCCACTGCAACCTCCGG GATGGAGTTTCCTGTTACCCAGGCTATAGTGCGATGGTGTGATCTCAGCCCACTGCAACCTCCGG A G DHTKD1 Ensembl:ENSG00000181192 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1000668810 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_312366,RMVar_hsa_circ_282118,RMVar_hsa_circ_142087,RMVar_hsa_circ_142086,RMVar_hsa_circ_316042,RMVar_hsa_circ_142100,RMVar_hsa_circ_266206,RMVar_hsa_circ_290574,RMVar_hsa_circ_142109,RMVar_hsa_circ_66717,RMVar_hsa_circ_142115,RMVar_hsa_circ_367073,RMVar_hsa_circ_70661,RMVar_hsa_circ_142116,RMVar_hsa_circ_93028,RMVar_hsa_circ_115817,RMVar_hsa_circ_142117,RMVar_hsa_circ_142121,RMVar_hsa_circ_142120,RMVar_hsa_circ_273375,RMVar_hsa_circ_142126,RMVar_hsa_circ_357999,RMVar_hsa_circ_99155,RMVar_hsa_circ_104834,RMVar_hsa_circ_56050,RMVar_hsa_circ_324932,RMVar_hsa_circ_142128,RMVar_hsa_circ_142129,RMVar_hsa_circ_142127,RMVar_hsa_circ_287548,RMVar_hsa_circ_360566,RMVar_hsa_circ_142139,RMVar_hsa_circ_96317,RMVar_hsa_circ_142137,RMVar_hsa_circ_316822,RMVar_hsa_circ_66117,RMVar_hsa_circ_142141,RMVar_hsa_circ_281640,RMVar_hsa_circ_309759,RMVar_hsa_circ_142140 38451 RMVar_ID_38451 Human_SNP_ID_422062024 A-to-I Human chr10 + 12116665 12116665 12116665 TGTCCACCTCTGCCTCCCAAAGTGCTGGGATTATAGGCATGAGCCACCGCGCCCAGTCTTTTTCT TGTCCACCTCTGCCTCCCAAAGTGCTGGGATTGTAGGCATGAGCCACCGCGCCCAGTCTTTTTCT A G DHTKD1 Ensembl:ENSG00000181192 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1281134833 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_312366,RMVar_hsa_circ_282118,RMVar_hsa_circ_142087,RMVar_hsa_circ_142086,RMVar_hsa_circ_316042,RMVar_hsa_circ_142100,RMVar_hsa_circ_266206,RMVar_hsa_circ_290574,RMVar_hsa_circ_142109,RMVar_hsa_circ_66717,RMVar_hsa_circ_142115,RMVar_hsa_circ_367073,RMVar_hsa_circ_70661,RMVar_hsa_circ_142116,RMVar_hsa_circ_93028,RMVar_hsa_circ_115817,RMVar_hsa_circ_142117,RMVar_hsa_circ_142121,RMVar_hsa_circ_142120,RMVar_hsa_circ_273375,RMVar_hsa_circ_142126,RMVar_hsa_circ_357999,RMVar_hsa_circ_99155,RMVar_hsa_circ_104834,RMVar_hsa_circ_56050,RMVar_hsa_circ_324932,RMVar_hsa_circ_142128,RMVar_hsa_circ_142129,RMVar_hsa_circ_142127,RMVar_hsa_circ_287548,RMVar_hsa_circ_360566,RMVar_hsa_circ_142139,RMVar_hsa_circ_96317,RMVar_hsa_circ_142137,RMVar_hsa_circ_316822,RMVar_hsa_circ_66117,RMVar_hsa_circ_142141,RMVar_hsa_circ_281640,RMVar_hsa_circ_309759,RMVar_hsa_circ_142140 38452 RMVar_ID_38452 Human_SNP_ID_422063944 A-to-I Human chr10 + 12121043 12121043 12121043 GGAGTTCGAGACCAGCCTGGCCAACACGGTGAAACCCCGCCTCTACTAAAAATACAAAAAATAGC GGAGTTCGAGACCAGCCTGGCCAACACGGTGACACCCCGCCTCTACTAAAAATACAAAAAATAGC A C DHTKD1 Ensembl:ENSG00000181192 Protein coding 3'UTR GSE47997;GSE126723:GSM3611827,GSM3611828,GSM3611829 K562 cells&HepG2 cells;Bronchiolar epithelium,BEP2D cell line - 23474544,31158229 RNA-Seq:(High) rs1371049258 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2146629,Human_miRNA_ID_2988053,Human_miRNA_ID_3021752 RMVar_hsa_circ_142116,RMVar_hsa_circ_93028,RMVar_hsa_circ_99155,RMVar_hsa_circ_142127,RMVar_hsa_circ_142148 38453 RMVar_ID_38453 Human_SNP_ID_422063986 A-to-I Human chr10 + 12121207 12121207 12121207 ACACCATTGCTGTCCAGCCTGGGTGACAGAGCAAGACTGCGTTTCAAAAAAAAAAAAAAAAAAAC ACACCATTGCTGTCCAGCCTGGGTGACAGAGCGAGACTGCGTTTCAAAAAAAAAAAAAAAAAAAC A G DHTKD1 Ensembl:ENSG00000181192 Protein coding 3'UTR GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-Seq:(High) rs1364051291 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4110060 Human_miRNA_ID_1264213,Human_miRNA_ID_1767310,Human_miRNA_ID_2611236,Human_miRNA_ID_2907495,Human_miRNA_ID_3026332 RMVar_hsa_circ_142116,RMVar_hsa_circ_93028,RMVar_hsa_circ_99155,RMVar_hsa_circ_142127,RMVar_hsa_circ_142148 38454 RMVar_ID_38454 Human_SNP_ID_422064552 A-to-I Human chr10 + 12123341 12123341 12123341 AGTTTAGGCTGGGCGTGGTAGCTCACGCCTGTAATCACAGCACTGTGGGAGGTCAAGATGGGTGC AGTTTAGGCTGGGCGTGGTAGCTCACGCCTGTTATCACAGCACTGTGGGAGGTCAAGATGGGTGC A T - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1027037358 Functional Loss SNV dbSNP153 33..33 33 - - - 38455 RMVar_ID_38455 Human_SNP_ID_422064629 A-to-I Human chr10 + 12123640 12123638 12123640 AGGTTACTTTAAATCTCTCCGAATTTCTTTTGAGACAGAGTCTCACTTTGTCGCCCAGGCTGGAG AGGTTACTTTAAATCTCTCCGAATTTCTTTT__GACAGAGTCTCACTTTGTCGCCCAGGCTGGAG TGA T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1178382563 Functional Loss DEL dbSNP153 32..33 33 - - - 38456 RMVar_ID_38456 Human_SNP_ID_422072140 A-to-I Human chr10 + 12150844 12150844 12150844 TTGCCCGGGCTGGAGTGCAGTGGCACAATCTCAGCTCACTGCAGCCTCTGTCTCCCGTGTTCAAG TTGCCCGGGCTGGAGTGCAGTGGCACAATCTCGGCTCACTGCAGCCTCTGTCTCCCGTGTTCAAG A G SEC61A2 Ensembl:ENSG00000065665 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1391920563 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_359737,RMVar_hsa_circ_101716,RMVar_hsa_circ_142152,RMVar_hsa_circ_52903,RMVar_hsa_circ_361325,RMVar_hsa_circ_142153 38457 RMVar_ID_38457 Human_SNP_ID_422072407 A-to-I Human chr10 + 12151800 12151800 12151800 ATTTTTGAGACGGAGTTTCACTCTTGTTGCCCAGGCTAGAGTACAATGGTGCAATCTCAGCTCGG ATTTTTGAGACGGAGTTTCACTCTTGTTGCCCGGGCTAGAGTACAATGGTGCAATCTCAGCTCGG A G SEC61A2 Ensembl:ENSG00000065665 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1178860520 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_359737,RMVar_hsa_circ_101716,RMVar_hsa_circ_142152,RMVar_hsa_circ_52903,RMVar_hsa_circ_361325,RMVar_hsa_circ_142153 38458 RMVar_ID_38458 Human_SNP_ID_422072608 A-to-I Human chr10 + 12152535 12152535 12152535 TAATTCCAGCACTTTGAGAGGCCGAGATGGGCAGTTCACTTGAGGTCAGGAGTTTGAGACCAGTC TAATTCCAGCACTTTGAGAGGCCGAGATGGGCCGTTCACTTGAGGTCAGGAGTTTGAGACCAGTC A C SEC61A2 Ensembl:ENSG00000065665 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs923355016 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_359737,RMVar_hsa_circ_101716,RMVar_hsa_circ_142152,RMVar_hsa_circ_52903,RMVar_hsa_circ_361325,RMVar_hsa_circ_142153 38459 RMVar_ID_38459 Human_SNP_ID_422080297 A-to-I Human chr10 - 12181807 12181807 12181807 ATTTATTTAATTTTTATTTTTTTAGTAGAGACAGAGTCTCACTATGTTGCCCAGGCTGGTCTCGA ATTTATTTAATTTTTATTTTTTTAGTAGAGACGGAGTCTCACTATGTTGCCCAGGCTGGTCTCGA T C NUDT5 Ensembl:ENSG00000165609 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs547891742 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2242197 RMVar_hsa_circ_116003,RMVar_hsa_circ_92417,RMVar_hsa_circ_23375,RMVar_hsa_circ_103054,RMVar_hsa_circ_142162,RMVar_hsa_circ_142163,RMVar_hsa_circ_114227,RMVar_hsa_circ_65111,RMVar_hsa_circ_142170,RMVar_hsa_circ_142171 38460 RMVar_ID_38460 Human_SNP_ID_422080318 A-to-I Human chr10 - 12181888 12181888 12181888 GTGATCCACCCACCTTGGCCTCCCAAAGTGCTAGGACTACAGTCGTGAGCCACCGCATCCGGCCA GTGATCCACCCACCTTGGCCTCCCAAAGTGCTCGGACTACAGTCGTGAGCCACCGCATCCGGCCA T G NUDT5 Ensembl:ENSG00000165609 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1448980825 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11284540 RMVar_hsa_circ_116003,RMVar_hsa_circ_92417,RMVar_hsa_circ_23375,RMVar_hsa_circ_103054,RMVar_hsa_circ_142162,RMVar_hsa_circ_142163,RMVar_hsa_circ_114227,RMVar_hsa_circ_65111,RMVar_hsa_circ_142170,RMVar_hsa_circ_142171 38461 RMVar_ID_38461 Human_SNP_ID_422087875 A-to-I Human chr10 + 12209704 12209704 12209704 CTCCCACCTCAGCCCCCCAAATAGCTGGGACTACAGGCGCATGCCACCTCGCCCAGCTAATTTCT CTCCCACCTCAGCCCCCCAAATAGCTGGGACTGCAGGCGCATGCCACCTCGCCCAGCTAATTTCT A G CDC123 Ensembl:ENSG00000151465 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs771621871 Functional Loss SNV dbSNP153 33..33 33 - - - 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_142178 38462 RMVar_ID_38462 Human_SNP_ID_422087883 A-to-I Human chr10 + 12209765 12209737 12209765 TTCTGTGTATTTTGTAGAGACAGGGTTTTGCCATGTAGTCCAAGCTGATCTCTACCTCCTGACCT TTCTG____________________________TGTAGTCCAAGCTGATCTCTACCTCCTGACCT GTGTATTTTGTAGAGACAGGGTTTTGCCA G CDC123 Ensembl:ENSG00000151465 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1421445763 Functional Loss DEL dbSNP153 6..33 33 - - - 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_142178 38463 RMVar_ID_38463 Human_SNP_ID_422087888 A-to-I Human chr10 + 12209754 12209754 12209754 GCCCAGCTAATTTCTGTGTATTTTGTAGAGACAGGGTTTTGCCATGTAGTCCAAGCTGATCTCTA GCCCAGCTAATTTCTGTGTATTTTGTAGAGACGGGGTTTTGCCATGTAGTCCAAGCTGATCTCTA A G CDC123 Ensembl:ENSG00000151465 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1242471852 Functional Loss SNV dbSNP153 33..33 33 - - - 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_142178 38464 RMVar_ID_38464 Human_SNP_ID_422087889 A-to-I Human chr10 + 12209765 12209765 12209765 TTCTGTGTATTTTGTAGAGACAGGGTTTTGCCATGTAGTCCAAGCTGATCTCTACCTCCTGACCT TTCTGTGTATTTTGTAGAGACAGGGTTTTGCCCTGTAGTCCAAGCTGATCTCTACCTCCTGACCT A C CDC123 Ensembl:ENSG00000151465 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs568539568 Functional Loss SNV dbSNP153 33..33 33 - - - 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_142178 38465 RMVar_ID_38465 Human_SNP_ID_422096600 A-to-I Human chr10 + 12240829 12240828 12240829 GAGGTTGAGGCTGCAGTGAGCCATGATCATACATGTCATGCCTAGCAGTGAACACCAGGTTGTGT GAGGTTGAGGCTGCAGTGAGCCATGATCATATGTGTCATGCCTAGCAGTGAACACCAGGTTGTGT CA TG CDC123 Ensembl:ENSG00000151465 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs386740953 Functional Loss MNV dbSNP153 32..33 33 - - - Human_RBP_ID_23220735 RMVar_hsa_circ_6787,RMVar_hsa_circ_88214,RMVar_hsa_circ_142178,RMVar_hsa_circ_292264,RMVar_hsa_circ_142188,RMVar_hsa_circ_25058,RMVar_hsa_circ_41148,RMVar_hsa_circ_78354,RMVar_hsa_circ_336904,RMVar_hsa_circ_142191 38466 RMVar_ID_38466 Human_SNP_ID_422096601 A-to-I Human chr10 + 12240829 12240828 12240829 GAGGTTGAGGCTGCAGTGAGCCATGATCATACATGTCATGCCTAGCAGTGAACACCAGGTTGTGT GAGGTTGAGGCTGCAGTGAGCCATGATCATAC_TGTCATGCCTAGCAGTGAACACCAGGTTGTGT CA C CDC123 Ensembl:ENSG00000151465 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1554749984 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_23220735 RMVar_hsa_circ_6787,RMVar_hsa_circ_88214,RMVar_hsa_circ_142178,RMVar_hsa_circ_292264,RMVar_hsa_circ_142188,RMVar_hsa_circ_25058,RMVar_hsa_circ_41148,RMVar_hsa_circ_78354,RMVar_hsa_circ_336904,RMVar_hsa_circ_142191 38467 RMVar_ID_38467 Human_SNP_ID_422096604 A-to-I Human chr10 + 12240829 12240829 12240829 GAGGTTGAGGCTGCAGTGAGCCATGATCATACATGTCATGCCTAGCAGTGAACACCAGGTTGTGT GAGGTTGAGGCTGCAGTGAGCCATGATCATACGTGTCATGCCTAGCAGTGAACACCAGGTTGTGT A G CDC123 Ensembl:ENSG00000151465 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6602569 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23220735 RMVar_hsa_circ_6787,RMVar_hsa_circ_88214,RMVar_hsa_circ_142178,RMVar_hsa_circ_292264,RMVar_hsa_circ_142188,RMVar_hsa_circ_25058,RMVar_hsa_circ_41148,RMVar_hsa_circ_78354,RMVar_hsa_circ_336904,RMVar_hsa_circ_142191 38468 RMVar_ID_38468 Human_SNP_ID_422096605 A-to-I Human chr10 + 12240829 12240829 12240829 GAGGTTGAGGCTGCAGTGAGCCATGATCATACATGTCATGCCTAGCAGTGAACACCAGGTTGTGT GAGGTTGAGGCTGCAGTGAGCCATGATCATACTTGTCATGCCTAGCAGTGAACACCAGGTTGTGT A T CDC123 Ensembl:ENSG00000151465 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6602569 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23220735 RMVar_hsa_circ_6787,RMVar_hsa_circ_88214,RMVar_hsa_circ_142178,RMVar_hsa_circ_292264,RMVar_hsa_circ_142188,RMVar_hsa_circ_25058,RMVar_hsa_circ_41148,RMVar_hsa_circ_78354,RMVar_hsa_circ_336904,RMVar_hsa_circ_142191 38469 RMVar_ID_38469 Human_SNP_ID_422097872 A-to-I Human chr10 + 12245355 12245355 12245355 ACGGCTCACAGTAGCCTTGACCTCCTGGGCTCAAGCAATCCTCCTACCTCAGCCCCCTAAGTAGC ACGGCTCACAGTAGCCTTGACCTCCTGGGCTCGAGCAATCCTCCTACCTCAGCCCCCTAAGTAGC A G CDC123 Ensembl:ENSG00000151465 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1166486522 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6787,RMVar_hsa_circ_88214,RMVar_hsa_circ_142178,RMVar_hsa_circ_292264,RMVar_hsa_circ_142188,RMVar_hsa_circ_25058,RMVar_hsa_circ_41148,RMVar_hsa_circ_78354,RMVar_hsa_circ_336904,RMVar_hsa_circ_142191 38470 RMVar_ID_38470 Human_SNP_ID_422098055 A-to-I Human chr10 + 12245949 12245949 12245949 AAAATTAGCTGCATGTGGTGGTGCATGCCTGTAGTCCCAGGTACTGAGGAGGCTGAGGCAGGAGG AAAATTAGCTGCATGTGGTGGTGCATGCCTGTCGTCCCAGGTACTGAGGAGGCTGAGGCAGGAGG A C CDC123 Ensembl:ENSG00000151465 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1366519177 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11286556 RMVar_hsa_circ_6787,RMVar_hsa_circ_88214,RMVar_hsa_circ_142178,RMVar_hsa_circ_292264,RMVar_hsa_circ_142188,RMVar_hsa_circ_25058,RMVar_hsa_circ_41148,RMVar_hsa_circ_78354,RMVar_hsa_circ_336904,RMVar_hsa_circ_142191 38471 RMVar_ID_38471 Human_SNP_ID_422098058 A-to-I Human chr10 + 12245955 12245955 12245955 AGCTGCATGTGGTGGTGCATGCCTGTAGTCCCAGGTACTGAGGAGGCTGAGGCAGGAGGATCCTT AGCTGCATGTGGTGGTGCATGCCTGTAGTCCCGGGTACTGAGGAGGCTGAGGCAGGAGGATCCTT A G CDC123 Ensembl:ENSG00000151465 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924157224 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11286556 RMVar_hsa_circ_6787,RMVar_hsa_circ_88214,RMVar_hsa_circ_142178,RMVar_hsa_circ_292264,RMVar_hsa_circ_142188,RMVar_hsa_circ_25058,RMVar_hsa_circ_41148,RMVar_hsa_circ_78354,RMVar_hsa_circ_336904,RMVar_hsa_circ_142191 38472 RMVar_ID_38472 Human_SNP_ID_422131028 A-to-I Human chr10 + 12357550 12357550 12357550 GTTGCCCAGGCTGGTCTAAAACTTCTGACGCCAAGTGATCTGCTCACCTCAGCCTCACAAAGTGG GTTGCCCAGGCTGGTCTAAAACTTCTGACGCCGAGTGATCTGCTCACCTCAGCCTCACAAAGTGG A G CAMK1D Ensembl:ENSG00000183049 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971456177 Functional Loss SNV dbSNP153 33..33 33 - - - 38473 RMVar_ID_38473 Human_SNP_ID_422134456 A-to-I Human chr10 + 12369213 12369213 12369213 GGAAAGGTAGGTACTGTTACCCCCACTTAAATATGAGAGACGAGAAACTCAGGAAGATGATGTAC GGAAAGGTAGGTACTGTTACCCCCACTTAAATGTGAGAGACGAGAAACTCAGGAAGATGATGTAC A G CAMK1D Ensembl:ENSG00000183049 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417213367 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23304172 38474 RMVar_ID_38474 Human_SNP_ID_422139075 A-to-I Human chr10 + 12386316 12386316 12386316 CAAAAATTAGTTGGGTATGGTGGTGTGTGCCTATGGTCCCAGCTACTCTGGAGACCAATAGGAGG CAAAAATTAGTTGGGTATGGTGGTGTGTGCCTGTGGTCCCAGCTACTCTGGAGACCAATAGGAGG A G CAMK1D Ensembl:ENSG00000183049 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1176444731 Functional Loss SNV dbSNP153 33..33 33 - - - 38475 RMVar_ID_38475 Human_SNP_ID_422139678 A-to-I Human chr10 + 12387758 12387758 12387758 GCGATCCGCCCACCCCAGCCTCCTAAAATGCTAGCATTACAGGCATGCGCTACCGTACCTGGCCT GCGATCCGCCCACCCCAGCCTCCTAAAATGCTGGCATTACAGGCATGCGCTACCGTACCTGGCCT A G CAMK1D Ensembl:ENSG00000183049 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1177766668 Functional Loss SNV dbSNP153 33..33 33 - - - 38476 RMVar_ID_38476 Human_SNP_ID_422145359 A-to-I Human chr10 + 12408078 12408078 12408078 CGGTGTTTTACCATGTTGGCCAGGCTGGTCTCAAACTCCTCACCTCACGTGATCCACCCACCTTG CGGTGTTTTACCATGTTGGCCAGGCTGGTCTCGAACTCCTCACCTCACGTGATCCACCCACCTTG A G CAMK1D Ensembl:ENSG00000183049 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1274018117 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_357603,RMVar_hsa_circ_355075 38477 RMVar_ID_38477 Human_SNP_ID_422145379 A-to-I Human chr10 + 12408140 12408140 12408140 TTGGCCTCCCAGAGTGCTGGGATTACAGGCATAAGCCACCGCGCCTGGCCTCTTTCATTTTCTTT TTGGCCTCCCAGAGTGCTGGGATTACAGGCATGAGCCACCGCGCCTGGCCTCTTTCATTTTCTTT A G CAMK1D Ensembl:ENSG00000183049 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1273624021 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_357603,RMVar_hsa_circ_355075 38478 RMVar_ID_38478 Human_SNP_ID_422158584 A-to-I Human chr10 + 12457670 12457670 12457670 GGGTGTAGTGGCGCGAGCCTGTAGTTCCAGCTACTTGGGAGGCTGAGGCAGGAGAATTGCTTGAA GGGTGTAGTGGCGCGAGCCTGTAGTTCCAGCTGCTTGGGAGGCTGAGGCAGGAGAATTGCTTGAA A G CAMK1D Ensembl:ENSG00000183049 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs927464533 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_357603,RMVar_hsa_circ_355075 38479 RMVar_ID_38479 Human_SNP_ID_422160651 A-to-I Human chr10 + 12465448 12465448 12465448 GTGATCTCGGCTCACTGCAAGCTCTGCCTGCCAGGTTCAAACGATTTTCCTGCCTCAGCCTTCCG GTGATCTCGGCTCACTGCAAGCTCTGCCTGCCGGGTTCAAACGATTTTCCTGCCTCAGCCTTCCG A G CAMK1D Ensembl:ENSG00000183049 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1181193120 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_357603,RMVar_hsa_circ_355075 38480 RMVar_ID_38480 Human_SNP_ID_422161318 A-to-I Human chr10 + 12468185 12468185 12468185 TCAAGTGATCCTCCCGCCTCAGCTTCCCGAGTAGCTGGGACTACAGGTGCTTAACACTACATCCA TCAAGTGATCCTCCCGCCTCAGCTTCCCGAGTGGCTGGGACTACAGGTGCTTAACACTACATCCA A G CAMK1D Ensembl:ENSG00000183049 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs954967265 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_357603,RMVar_hsa_circ_355075 38481 RMVar_ID_38481 Human_SNP_ID_422164412 A-to-I Human chr10 + 12480288 12480288 12480288 GAAATCCGGTCTCTACTAAAAATACAAAAATTAGCTGGACGTGATAGCGCACGCCTGCAATCTCA GAAATCCGGTCTCTACTAAAAATACAAAAATTGGCTGGACGTGATAGCGCACGCCTGCAATCTCA A G CAMK1D Ensembl:ENSG00000183049 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1043661651 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_357603,RMVar_hsa_circ_355075 38482 RMVar_ID_38482 Human_SNP_ID_422182296 A-to-I Human chr10 + 12545343 12545343 12545343 ATGGTGGTGTGCGTCTGTAGTTTTAGCTACTCAGGATACTGAGGCAGGAGAATTGCTTGAACCCC ATGGTGGTGTGCGTCTGTAGTTTTAGCTACTCTGGATACTGAGGCAGGAGAATTGCTTGAACCCC A T CAMK1D Ensembl:ENSG00000183049 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1179513124 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_357603,RMVar_hsa_circ_142197,RMVar_hsa_circ_355075,RMVar_hsa_circ_142198 38483 RMVar_ID_38483 Human_SNP_ID_422199271 A-to-I Human chr10 + 12606897 12606897 12606897 GTCACCGGGCTGGAGTGCCGTGGCGCAGTCTCAGCTCACTGCAACCTCCGCCTCCTGGGTTCAAG GTCACCGGGCTGGAGTGCCGTGGCGCAGTCTCGGCTCACTGCAACCTCCGCCTCCTGGGTTCAAG A G CAMK1D Ensembl:ENSG00000183049 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1198763441 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9671 38484 RMVar_ID_38484 Human_SNP_ID_422246219 A-to-I Human chr10 + 12778824 12778824 12778824 GAGCCCAGGACTTTGAGGCAACGGCGAACTATAAGCACACCACTGCACTCCAGCCTGGGCAACAG GAGCCCAGGACTTTGAGGCAACGGCGAACTATGAGCACACCACTGCACTCCAGCCTGGGCAACAG A G CAMK1D Ensembl:ENSG00000183049 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1377977638 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15754,RMVar_hsa_circ_327239,RMVar_hsa_circ_327076,RMVar_hsa_circ_142202 38485 RMVar_ID_38485 Human_SNP_ID_422253439 A-to-I Human chr10 + 12804858 12804858 12804858 TACTCAGGAAGTTGAGGCAGGAGGATTGTATGAGCCTGGGAGTTCAAGGCTGCAGTGAGCTATGA TACTCAGGAAGTTGAGGCAGGAGGATTGTATGGGCCTGGGAGTTCAAGGCTGCAGTGAGCTATGA A G CAMK1D Ensembl:ENSG00000183049 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1245334786 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15754,RMVar_hsa_circ_142203,RMVar_hsa_circ_312934 38486 RMVar_ID_38486 Human_SNP_ID_422259194 A-to-I Human chr10 + 12826052 12826052 12826052 TCAGCTACTTGGGAGGCTGAGGCAGGAGAATCACTTGAACCCAGGAAGCGGAGGTTGCAATGAGC TCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCAGGAAGCGGAGGTTGCAATGAGC A G CAMK1D Ensembl:ENSG00000183049 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1178023046 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_142206 38487 RMVar_ID_38487 Human_SNP_ID_422259195 A-to-I Human chr10 + 12826057 12826057 12826057 TACTTGGGAGGCTGAGGCAGGAGAATCACTTGAACCCAGGAAGCGGAGGTTGCAATGAGCTGAGA TACTTGGGAGGCTGAGGCAGGAGAATCACTTGGACCCAGGAAGCGGAGGTTGCAATGAGCTGAGA A G CAMK1D Ensembl:ENSG00000183049 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs938418755 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_142206 38488 RMVar_ID_38488 Human_SNP_ID_422306087 A-to-I Human chr10 - 12994973 12994973 12994973 GGGTTCAAGTGATTCTCCTGCCTCAGCTTCCCAAGTAGTTGGGATTACAGGTATGTGCCATCACA GGGTTCAAGTGATTCTCCTGCCTCAGCTTCCCCAGTAGTTGGGATTACAGGTATGTGCCATCACA T G CCDC3 Ensembl:ENSG00000151468 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1245794119 Functional Loss SNV dbSNP153 33..33 33 - - - 38489 RMVar_ID_38489 Human_SNP_ID_422357961 A-to-I Human chr10 + 13189584 13189584 13189584 ACCTCAGGTGATCTGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGCTC ACCTCAGGTGATCTGCCTGCCTCGGCCTCCCAGAGTGCTGGGATTACAGGCATGAGCCACTGCTC A G MCM10 Ensembl:ENSG00000065328 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1564388394 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2167,RMVar_hsa_circ_81574,RMVar_hsa_circ_1610,RMVar_hsa_circ_142229,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_142239,RMVar_hsa_circ_312487,RMVar_hsa_circ_351363,RMVar_hsa_circ_285682 38490 RMVar_ID_38490 Human_SNP_ID_422365368 A-to-I Human chr10 + 13218895 13218895 13218895 AACATTTTTAAACATTTATAATTTTAAACATTATAAGATCACAGAGTATATCAGAGTTCTCAATT AACATTTTTAAACATTTATAATTTTAAACATTGTAAGATCACAGAGTATATCAGAGTTCTCAATT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1284584849 Functional Loss SNV dbSNP153 33..33 33 - - - 38491 RMVar_ID_38491 Human_SNP_ID_422391585 A-to-I Human chr10 - 13309210 13309210 13309210 TTTCCCAGGCTAGTCTTGAAATCCTGGGCTCAAGTGATCGTCCCACTCTGGCCTCCCAAAGTGTT TTTCCCAGGCTAGTCTTGAAATCCTGGGCTCAGGTGATCGTCCCACTCTGGCCTCCCAAAGTGTT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1227654521 Functional Loss SNV dbSNP153 33..33 33 - - - 38492 RMVar_ID_38492 Human_SNP_ID_422395043 A-to-I Human chr10 - 13320789 13320789 13320789 AGTTTTCCTCTTGTCACCCAGGCTGGAGTGCAATGGCGCGATCTCAGCTCACTGCAACCTCCCCC AGTTTTCCTCTTGTCACCCAGGCTGGAGTGCAGTGGCGCGATCTCAGCTCACTGCAACCTCCCCC T C SEPHS1 Ensembl:ENSG00000086475 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1015241257 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91740,RMVar_hsa_circ_96146,RMVar_hsa_circ_92430,RMVar_hsa_circ_142251,RMVar_hsa_circ_142252,RMVar_hsa_circ_142250 38493 RMVar_ID_38493 Human_SNP_ID_422397095 A-to-I Human chr10 - 13326742 13326742 13326742 ATCACTTGAGTCCAGCAGTTGGAGACCAGCCTAGGCAACATAGTGAGACCCCATCTCGTCTCTTT ATCACTTGAGTCCAGCAGTTGGAGACCAGCCTGGGCAACATAGTGAGACCCCATCTCGTCTCTTT T C SEPHS1 Ensembl:ENSG00000086475 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973795200 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96146,RMVar_hsa_circ_92430,RMVar_hsa_circ_142251,RMVar_hsa_circ_142254,RMVar_hsa_circ_377689,RMVar_hsa_circ_142250,RMVar_hsa_circ_320424 38494 RMVar_ID_38494 Human_SNP_ID_422397096 A-to-I Human chr10 - 13326742 13326742 13326742 ATCACTTGAGTCCAGCAGTTGGAGACCAGCCTAGGCAACATAGTGAGACCCCATCTCGTCTCTTT ATCACTTGAGTCCAGCAGTTGGAGACCAGCCTCGGCAACATAGTGAGACCCCATCTCGTCTCTTT T G SEPHS1 Ensembl:ENSG00000086475 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973795200 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96146,RMVar_hsa_circ_92430,RMVar_hsa_circ_142251,RMVar_hsa_circ_142254,RMVar_hsa_circ_377689,RMVar_hsa_circ_142250,RMVar_hsa_circ_320424 38495 RMVar_ID_38495 Human_SNP_ID_422401360 A-to-I Human chr10 - 13341740 13341738 13341741 GTTGGTCAGGCTGGTCTGGAACTCCTGACTCTAAGTGATCTGCCCACCTCGGCCTCCCAAAGTGC GTTGGTCAGGCTGGTCTGGAACTCCTGACTC___GTGATCTGCCCACCTCGGCCTCCCAAAGTGC CTTA C SEPHS1 Ensembl:ENSG00000086475 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1181453540 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_11313647,Human_RBP_ID_24794909 RMVar_hsa_circ_142254,RMVar_hsa_circ_320424,RMVar_hsa_circ_319143,RMVar_hsa_circ_142256,RMVar_hsa_circ_291955 38496 RMVar_ID_38496 Human_SNP_ID_422401407 A-to-I Human chr10 - 13341912 13341912 13341912 TGAGTACAGTGGTGCAATCTCAGCTCACTGCAACCTCTGCCTCCCGGGTTCAAGGCCCTCCCAGG TGAGTACAGTGGTGCAATCTCAGCTCACTGCAGCCTCTGCCTCCCGGGTTCAAGGCCCTCCCAGG T C SEPHS1 Ensembl:ENSG00000086475 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1249562326 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_142254,RMVar_hsa_circ_320424,RMVar_hsa_circ_319143,RMVar_hsa_circ_142256,RMVar_hsa_circ_291955 38497 RMVar_ID_38497 Human_SNP_ID_422401753 A-to-I Human chr10 - 13342874 13342874 13342874 AAAGTTACCTGGGCTTGCTGGTGTACACCTGTAGTTTCAGCTACTCGGGAGGCTGAGGTGGGAGG AAAGTTACCTGGGCTTGCTGGTGTACACCTGTGGTTTCAGCTACTCGGGAGGCTGAGGTGGGAGG T C SEPHS1 Ensembl:ENSG00000086475 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs959947785 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24794919 RMVar_hsa_circ_142254,RMVar_hsa_circ_320424,RMVar_hsa_circ_319143,RMVar_hsa_circ_142256,RMVar_hsa_circ_291955 38498 RMVar_ID_38498 Human_SNP_ID_422465930 A-to-I Human chr10 - 13585955 13585955 13585955 AGGTGGACAGATCACCTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAGCATGGTGAAATCCCGTC AGGTGGACAGATCACCTGAGGTCAGGAGTTCAGGACCAGCCTGGCCAGCATGGTGAAATCCCGTC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs776186395 Functional Loss SNV dbSNP153 33..33 33 - - - 38499 RMVar_ID_38499 Human_SNP_ID_422470236 A-to-I Human chr10 + 13602807 13602807 13602807 CAGGCTGGAGTGCAGTGGCATGATGTAGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGAGTTT CAGGCTGGAGTGCAGTGGCATGATGTAGGCTCGCTGCAACCTCCGCCTCCCGGGTTCAAGAGTTT A G PRPF18 Ensembl:ENSG00000165630 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1021446245 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_65310,RMVar_hsa_circ_365287,RMVar_hsa_circ_349065,RMVar_hsa_circ_142261 38500 RMVar_ID_38500 Human_SNP_ID_422479772 A-to-I Human chr10 + 13640132 13640132 13640132 CTGAGGTACCAGTTACCAGGAGAGTGGTGTCCACGCCTGAGAGGTTTCACTCCCAGCTCCTGGAA CTGAGGTACCAGTTACCAGGAGAGTGGTGTCCGCGCCTGAGAGGTTTCACTCCCAGCTCCTGGAA A G AL157392.3,AL157392.5 Ensembl:ENSG00000239665,Ensembl:ENSG00000282246 lincRNA,Protein coding intron,intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs991006876 Functional Loss SNV dbSNP153 33..33 33 - - - 38501 RMVar_ID_38501 Human_SNP_ID_422493174 A-to-I Human chr10 - 13683952 13683952 13683952 GTAATCCCAGCACTTTGGGAGTCAAGGCGGGCAGATCACTTGAGGTCAGCAGTTGGAGACCAGCC GTAATCCCAGCACTTTGGGAGTCAAGGCGGGCCGATCACTTGAGGTCAGCAGTTGGAGACCAGCC T G FRMD4A Ensembl:ENSG00000151474 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1473397247 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2861,RMVar_hsa_circ_142266,RMVar_hsa_circ_91908,RMVar_hsa_circ_121868,RMVar_hsa_circ_126994,RMVar_hsa_circ_93841,RMVar_hsa_circ_83921,RMVar_hsa_circ_11231,RMVar_hsa_circ_142268,RMVar_hsa_circ_142269,RMVar_hsa_circ_142270,RMVar_hsa_circ_142267,RMVar_hsa_circ_35794,RMVar_hsa_circ_358585,RMVar_hsa_circ_12946,RMVar_hsa_circ_373534,RMVar_hsa_circ_125328,RMVar_hsa_circ_142276,RMVar_hsa_circ_142280,RMVar_hsa_circ_24803,RMVar_hsa_circ_42070,RMVar_hsa_circ_88844,RMVar_hsa_circ_142285 38502 RMVar_ID_38502 Human_SNP_ID_422514686 A-to-I Human chr10 - 13760397 13760397 13760397 CTCCTGCCTCAGCCTCCCAAGTTGCTGGGACTACAGGCATGAGTCACTGCACCGGGCTAATTATT CTCCTGCCTCAGCCTCCCAAGTTGCTGGGACTTCAGGCATGAGTCACTGCACCGGGCTAATTATT T A FRMD4A Ensembl:ENSG00000151474 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs555059015 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3651,RMVar_hsa_circ_91908,RMVar_hsa_circ_121868,RMVar_hsa_circ_93841,RMVar_hsa_circ_142268,RMVar_hsa_circ_142269,RMVar_hsa_circ_142270,RMVar_hsa_circ_12946,RMVar_hsa_circ_88844,RMVar_hsa_circ_6410,RMVar_hsa_circ_142285,RMVar_hsa_circ_345356,RMVar_hsa_circ_358012,RMVar_hsa_circ_320102,RMVar_hsa_circ_303033,RMVar_hsa_circ_309994,RMVar_hsa_circ_3300,RMVar_hsa_circ_6481 38503 RMVar_ID_38503 Human_SNP_ID_422571378 A-to-I Human chr10 - 13967843 13967843 13967843 TGGGGTTTCGCCATGTCGTCCAGACTGGTCTCAAACTCCTGGGCTCACGCCATCTGCCTGCCCCA TGGGGTTTCGCCATGTCGTCCAGACTGGTCTCCAACTCCTGGGCTCACGCCATCTGCCTGCCCCA T G FRMD4A Ensembl:ENSG00000151474 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1168907840 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3651,RMVar_hsa_circ_88844,RMVar_hsa_circ_142285 38504 RMVar_ID_38504 Human_SNP_ID_422578701 A-to-I Human chr10 - 13994347 13994347 13994347 TGGTGAAACCCCATCTCTACTAAAATACAAAAATTAGCTGAGTGTGGTGGGGCACGCCTGTAGTC TGGTGAAACCCCATCTCTACTAAAATACAAAAGTTAGCTGAGTGTGGTGGGGCACGCCTGTAGTC T C FRMD4A Ensembl:ENSG00000151474 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs975971083 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3651 38505 RMVar_ID_38505 Human_SNP_ID_422597742 A-to-I Human chr10 - 14062819 14062819 14062819 TGCAATGGCATGATCTCACTGCAACCTCCCAAAGTGCTGGAATTACACACGTGAGCCACTGTGCC TGCAATGGCATGATCTCACTGCAACCTCCCAACGTGCTGGAATTACACACGTGAGCCACTGTGCC T G FRMD4A Ensembl:ENSG00000151474 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1236114205 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3651 38506 RMVar_ID_38506 Human_SNP_ID_422619596 A-to-I Human chr10 - 14139594 14139594 14139594 CACAAAAAAATTAGCCCAGTGTGGTGGTATGCACTTGTGGTCCCAGCTACTTGGGAGGCTGAAGT CACAAAAAAATTAGCCCAGTGTGGTGGTATGCGCTTGTGGTCCCAGCTACTTGGGAGGCTGAAGT T C FRMD4A Ensembl:ENSG00000151474 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1290741086 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3651 38507 RMVar_ID_38507 Human_SNP_ID_422619760 A-to-I Human chr10 - 14140222 14140222 14140222 CCCATCTCTGCTAAAAAATACGAAGATTAGCCAGGTGTGGTGGTGTGCGCCTGTAGTCCCAGCGA CCCATCTCTGCTAAAAAATACGAAGATTAGCCGGGTGTGGTGGTGTGCGCCTGTAGTCCCAGCGA T C FRMD4A Ensembl:ENSG00000151474 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs928772879 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3651 38508 RMVar_ID_38508 Human_SNP_ID_422639043 A-to-I Human chr10 - 14209193 14209193 14209193 AAATTATCAAGTGTCAGGAGAAGAAAAGTGTCAGGAGAGACACACAGAGGAGGATGCCATGTGAA AAATTATCAAGTGTCAGGAGAAGAAAAGTGTCGGGAGAGACACACAGAGGAGGATGCCATGTGAA T C FRMD4A Ensembl:ENSG00000151474 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1434126327 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3651 38509 RMVar_ID_38509 Human_SNP_ID_422640878 A-to-I Human chr10 - 14216436 14216436 14216436 GAACTCCTGAGCTCAAGTGATGCACCCTCCTCAGACTCCCAAAGAATTGAGATTACAGGCATGAG GAACTCCTGAGCTCAAGTGATGCACCCTCCTCCGACTCCCAAAGAATTGAGATTACAGGCATGAG T G FRMD4A Ensembl:ENSG00000151474 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs564529245 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3651 38510 RMVar_ID_38510 Human_SNP_ID_422644676 A-to-I Human chr10 - 14229597 14229597 14229597 CTGTCTCTACATCTTTTTTTAAAAATTAGCCAAGCATTGTGGTGCACACCTGTAGTCCCAGCTAC CTGTCTCTACATCTTTTTTTAAAAATTAGCCAGGCATTGTGGTGCACACCTGTAGTCCCAGCTAC T C FRMD4A Ensembl:ENSG00000151474 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs533422869 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3651 38511 RMVar_ID_38511 Human_SNP_ID_422656571 A-to-I Human chr10 - 14274871 14274870 14274871 ACCGAAATAGCAGAAGGGTGAGGACCTGGAAAAGGAAGGGTCAGGTGACTCCTGGGAGCATCCCT ACCGAAATAGCAGAAGGGTGAGGACCTGGAAA_GGAAGGGTCAGGTGACTCCTGGGAGCATCCCT CT C FRMD4A Ensembl:ENSG00000151474 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs35762654 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_3651 38512 RMVar_ID_38512 Human_SNP_ID_422664386 A-to-I Human chr10 - 14305726 14305726 14305726 TTCTTTATCCAGTCTGTCATTGACGGGCATTTAGGTTGATTTCATGTCTTTGCTATTGTGAATAG TTCTTTATCCAGTCTGTCATTGACGGGCATTTGGGTTGATTTCATGTCTTTGCTATTGTGAATAG T C FRMD4A Ensembl:ENSG00000151474 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs555934540 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3651 38513 RMVar_ID_38513 Human_SNP_ID_422736032 A-to-I Human chr10 - 14570680 14570680 14570680 CTTCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGAACTCGCCACCATGCCCAGCTGATTTTT CTTCTGCCTCAGCCTCCCAAGTAGCTGGGATTGCAGGAACTCGCCACCATGCCCAGCTGATTTTT T C FAM107B Ensembl:ENSG00000065809 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1324003478 Functional Loss SNV dbSNP153 33..33 33 - - - 38514 RMVar_ID_38514 Human_SNP_ID_422739468 A-to-I Human chr10 - 14582821 14582821 14582821 TTGGCCTCCCAAAGTGCTGGGATTATAGGCGTAAGCCACCATGCCCGGCGAGTTTCGTCTTTCTT TTGGCCTCCCAAAGTGCTGGGATTATAGGCGTGAGCCACCATGCCCGGCGAGTTTCGTCTTTCTT T C FAM107B Ensembl:ENSG00000065809 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs966631671 Functional Loss SNV dbSNP153 33..33 33 - - - 38515 RMVar_ID_38515 Human_SNP_ID_422739473 A-to-I Human chr10 - 14582829 14582829 14582829 CACGTGCCTTGGCCTCCCAAAGTGCTGGGATTATAGGCGTAAGCCACCATGCCCGGCGAGTTTCG CACGTGCCTTGGCCTCCCAAAGTGCTGGGATTGTAGGCGTAAGCCACCATGCCCGGCGAGTTTCG T C FAM107B Ensembl:ENSG00000065809 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1465005000 Functional Loss SNV dbSNP153 33..33 33 - - - 38516 RMVar_ID_38516 Human_SNP_ID_422806472 A-to-I Human chr10 - 14830833 14830833 14830833 TTGTCTTGTTTTGTTTTTTGAGACGGAGTTTCACTCTTGTCGCCCAGACTGGAGTATAATGGTGT TTGTCTTGTTTTGTTTTTTGAGACGGAGTTTCCCTCTTGTCGCCCAGACTGGAGTATAATGGTGT T G CDNF Ensembl:ENSG00000185267 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1333218994 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_360289 38517 RMVar_ID_38517 Human_SNP_ID_422826244 A-to-I Human chr10 + 14905902 14905901 14905902 TACTTGGGAGGCTGAGGCAGGAAAATCACTTGAACCCTGGAGGCTGAGGTTGCAGTGAGCTGAGA TACTTGGGAGGCTGAGGCAGGAAAATCACTTG_ACCCTGGAGGCTGAGGTTGCAGTGAGCTGAGA GA G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1187647394 Functional Loss DEL dbSNP153 33..33 33 - - - 38518 RMVar_ID_38518 Human_SNP_ID_422826253 A-to-I Human chr10 - 14905948 14905948 14905948 AGATGGAGTCTCGCTCTGTCACTCAGGCTGGAATGCAGTGGCCCTATCTCAGCTCACTGCAACCT AGATGGAGTCTCGCTCTGTCACTCAGGCTGGAGTGCAGTGGCCCTATCTCAGCTCACTGCAACCT T C DCLRE1C Ensembl:ENSG00000152457 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7903879 Functional Loss SNV dbSNP153 33..33 33 - - - 38519 RMVar_ID_38519 Human_SNP_ID_422826517 A-to-I Human chr10 + 14906943 14906943 14906943 GCTTTGTTGCCCAGGCTGGGCACAATCAGCTCACTGCAGTTTCAACCTCCTGGGCTCAATCCATC GCTTTGTTGCCCAGGCTGGGCACAATCAGCTCCCTGCAGTTTCAACCTCCTGGGCTCAATCCATC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs548621987 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19494759,Human_RBP_ID_24796032 38520 RMVar_ID_38520 Human_SNP_ID_422826534 A-to-I Human chr10 - 14907007 14907007 14907007 AATGTTAGCCAGACATGGTGGTGTGCACCTGTAGTCCTCGCTACTTGGAAGGCTTAGGTGGCAGG AATGTTAGCCAGACATGGTGGTGTGCACCTGTGGTCCTCGCTACTTGGAAGGCTTAGGTGGCAGG T C DCLRE1C Ensembl:ENSG00000152457 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1257281252 Functional Loss SNV dbSNP153 33..33 33 - - - 38521 RMVar_ID_38521 Human_SNP_ID_422827149 A-to-I Human chr10 - 14908597 14908597 14908597 GAACCAACTACTCTAAGCAGTGAGACACATATACCCGAGGAAAAAAGTTTGCTAAATCTTAGCAC GAACCAACTACTCTAAGCAGTGAGACACATATGCCCGAGGAAAAAAGTTTGCTAAATCTTAGCAC T C DCLRE1C Ensembl:ENSG00000152457 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs201350418 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17679774,Human_RBP_ID_27405055 38522 RMVar_ID_38522 Human_SNP_ID_422828692 A-to-I Human chr10 + 14913062 14913062 14913062 TGTTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGGTCTCGATCTCTCTGACCTCATG TGTTTTTAGTAGAGACGGGGTTTCACCGTGTTGGCCAGGATGGTCTCGATCTCTCTGACCTCATG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1212619971 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8330524,Human_RBP_ID_11319003 38523 RMVar_ID_38523 Human_SNP_ID_422833586 A-to-I Human chr10 - 14930185 14930185 14930185 ATTGCTTGAGTTTGGGAGGTGGAGGTTGCAGTAAGCCAAGATTGTACCACTGCACTCCAGCCTGG ATTGCTTGAGTTTGGGAGGTGGAGGTTGCAGTGAGCCAAGATTGTACCACTGCACTCCAGCCTGG T C DCLRE1C Ensembl:ENSG00000152457 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1464973979 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95450,RMVar_hsa_circ_44299,RMVar_hsa_circ_142324,RMVar_hsa_circ_346745,RMVar_hsa_circ_305070,RMVar_hsa_circ_305870,RMVar_hsa_circ_142326,RMVar_hsa_circ_330815,RMVar_hsa_circ_18230,RMVar_hsa_circ_294230,RMVar_hsa_circ_142327,RMVar_hsa_circ_273362,RMVar_hsa_circ_142328,RMVar_hsa_circ_142329 38524 RMVar_ID_38524 Human_SNP_ID_422833720 A-to-I Human chr10 - 14930463 14930463 14930463 TCACCACTGCACTCCAGTCTGGGTGACAGAGCAAGACTCTGCCTCAAAAAAAACAAACAAAACCC TCACCACTGCACTCCAGTCTGGGTGACAGAGCCAGACTCTGCCTCAAAAAAAACAAACAAAACCC T G DCLRE1C Ensembl:ENSG00000152457 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1457251281 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95450,RMVar_hsa_circ_44299,RMVar_hsa_circ_142324,RMVar_hsa_circ_346745,RMVar_hsa_circ_305070,RMVar_hsa_circ_305870,RMVar_hsa_circ_142326,RMVar_hsa_circ_330815,RMVar_hsa_circ_18230,RMVar_hsa_circ_294230,RMVar_hsa_circ_142327,RMVar_hsa_circ_273362,RMVar_hsa_circ_142328,RMVar_hsa_circ_142329 38525 RMVar_ID_38525 Human_SNP_ID_422836071 A-to-I Human chr10 - 14937640 14937640 14937640 GGGATTCGTTCACCTTGGCCTCCCAAAGTGCTAGAATTACAGGCATGAGCCACCGCACCTGGCTC GGGATTCGTTCACCTTGGCCTCCCAAAGTGCTGGAATTACAGGCATGAGCCACCGCACCTGGCTC T C DCLRE1C Ensembl:ENSG00000152457 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs959829036 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95450,RMVar_hsa_circ_44299,RMVar_hsa_circ_18230,RMVar_hsa_circ_294230,RMVar_hsa_circ_142327,RMVar_hsa_circ_142329,RMVar_hsa_circ_333598,RMVar_hsa_circ_297947,RMVar_hsa_circ_58901,RMVar_hsa_circ_5704,RMVar_hsa_circ_352602,RMVar_hsa_circ_332014,RMVar_hsa_circ_142330 38526 RMVar_ID_38526 Human_SNP_ID_422837738 A-to-I Human chr10 - 14943017 14943005 14943017 GTTCAAGCAATTCTCCCTGCCTCCGCCTCCCTAGTGGCTGGGATTACAGGCCTGAACCACCACAC GTTCAAGCAATTCTCCCTGCCTCCGCCTCCCT____________TACAGGCCTGAACCACCACAC AATCCCAGCCACT A DCLRE1C Ensembl:ENSG00000152457 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1208838978 Functional Loss DEL dbSNP153 33..44 33 - - - RMVar_hsa_circ_44299,RMVar_hsa_circ_18230,RMVar_hsa_circ_294230,RMVar_hsa_circ_142329,RMVar_hsa_circ_333598,RMVar_hsa_circ_297947,RMVar_hsa_circ_352602,RMVar_hsa_circ_332014,RMVar_hsa_circ_142330,RMVar_hsa_circ_142331,RMVar_hsa_circ_330207 38527 RMVar_ID_38527 Human_SNP_ID_422838712 A-to-I Human chr10 - 14946125 14946123 14946125 GTGCGCATGTAGTCCCAGCTACTCAAGAGGCTAAGACAGGAGAATCGCTTGAACCCGGGAGGCGG GTGCGCATGTAGTCCCAGCTACTCAAGAGGCT__GACAGGAGAATCGCTTGAACCCGGGAGGCGG CTT C DCLRE1C Ensembl:ENSG00000152457 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1171086885 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_142333,RMVar_hsa_circ_114700,RMVar_hsa_circ_318037,RMVar_hsa_circ_16879,RMVar_hsa_circ_142332 38528 RMVar_ID_38528 Human_SNP_ID_422838713 A-to-I Human chr10 - 14946125 14946125 14946125 GTGCGCATGTAGTCCCAGCTACTCAAGAGGCTAAGACAGGAGAATCGCTTGAACCCGGGAGGCGG GTGCGCATGTAGTCCCAGCTACTCAAGAGGCTGAGACAGGAGAATCGCTTGAACCCGGGAGGCGG T C DCLRE1C Ensembl:ENSG00000152457 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1029824852 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_142333,RMVar_hsa_circ_114700,RMVar_hsa_circ_318037,RMVar_hsa_circ_16879,RMVar_hsa_circ_142332 38529 RMVar_ID_38529 Human_SNP_ID_422839008 A-to-I Human chr10 - 14947136 14947136 14947136 GTGATGTTGGCTCACTGCAATCTCTGCCTCCCAGGTTCAAGCAATTCTCCCAGCTCAGCCTCCCA GTGATGTTGGCTCACTGCAATCTCTGCCTCCCGGGTTCAAGCAATTCTCCCAGCTCAGCCTCCCA T C DCLRE1C Ensembl:ENSG00000152457 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs550784609 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_142333,RMVar_hsa_circ_114700,RMVar_hsa_circ_318037,RMVar_hsa_circ_16879,RMVar_hsa_circ_142332 38530 RMVar_ID_38530 Human_SNP_ID_315324718 A-to-I Human chr7 + 30141785 30141785 30141785 TCTCAAGCAGCTCTTCCGCCTTGGCCTCCCACAATGTTGGAATTACAGGTGTGAGCCACCAGGCC TCTCAAGCAGCTCTTCCGCCTTGGCCTCCCACGATGTTGGAATTACAGGTGTGAGCCACCAGGCC A G MTURN Ensembl:ENSG00000180354 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1242717570 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118245,RMVar_hsa_circ_244320 38531 RMVar_ID_38531 Human_SNP_ID_315379631 A-to-I Human chr7 + 30372607 30372607 30372607 TATGCCAGGAGCATCAGGCTGAAGTGAAGGGCATGTGCACAGAAACCGGCATGTATGCCCTGAGT TATGCCAGGAGCATCAGGCTGAAGTGAAGGGCCTGTGCACAGAAACCGGCATGTATGCCCTGAGT A C AC006978.2,AC006978.1 Ensembl:ENSG00000281593,Ensembl:ENSG00000235859 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048908171 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_955617,Human_RBP_ID_5105358,Human_RBP_ID_8273197,Human_RBP_ID_10370360,Human_RBP_ID_21960795 RMVar_hsa_circ_244336 38532 RMVar_ID_38532 Human_SNP_ID_315379632 A-to-I Human chr7 + 30372607 30372607 30372607 TATGCCAGGAGCATCAGGCTGAAGTGAAGGGCATGTGCACAGAAACCGGCATGTATGCCCTGAGT TATGCCAGGAGCATCAGGCTGAAGTGAAGGGCGTGTGCACAGAAACCGGCATGTATGCCCTGAGT A G AC006978.2,AC006978.1 Ensembl:ENSG00000281593,Ensembl:ENSG00000235859 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048908171 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_955617,Human_RBP_ID_5105358,Human_RBP_ID_8273197,Human_RBP_ID_10370360,Human_RBP_ID_21960795 RMVar_hsa_circ_244336 38533 RMVar_ID_38533 Human_SNP_ID_315380012 A-to-I Human chr7 + 30373808 30373808 30373808 ACAAAAATTAGCTGGGCGTGGTGCGCGCCTGTAGTTCCAGCTACTCAGGAGGCCGAGGCAGGAGA ACAAAAATTAGCTGGGCGTGGTGCGCGCCTGTGGTTCCAGCTACTCAGGAGGCCGAGGCAGGAGA A G AC006978.2 Ensembl:ENSG00000281593 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1380797146 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_244336 38534 RMVar_ID_38534 Human_SNP_ID_315380029 A-to-I Human chr7 + 30373874 30373873 30373874 TTGCTTGAACCCAGGAGGCAGAGGTTGCAGTGAACTGAGATTGTGCCACTGTACTCCAACCTGGC TTGCTTGAACCCAGGAGGCAGAGGTTGCAGTG_ACTGAGATTGTGCCACTGTACTCCAACCTGGC GA G AC006978.2 Ensembl:ENSG00000281593 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1236866565 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_244336 38535 RMVar_ID_38535 Human_SNP_ID_315383849 A-to-I Human chr7 + 30387563 30387563 30387563 CCAGCTATTCTGGAGGCTGAGATGGGAGGATCACTTGAACCCAGGAGGTTGAGGCTGCAGTGAGT CCAGCTATTCTGGAGGCTGAGATGGGAGGATCGCTTGAACCCAGGAGGTTGAGGCTGCAGTGAGT A G AC006978.2 Ensembl:ENSG00000281593 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1253282181 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_244336 38536 RMVar_ID_38536 Human_SNP_ID_315396213 A-to-I Human chr7 + 30429910 30429910 30429910 GGGCATGGTGGTGTGCACCTGTACTCCCAGCTACTCGGGAGACTGAGGTAGGAGAATTGCTTGAA GGGCATGGTGGTGTGCACCTGTACTCCCAGCTCCTCGGGAGACTGAGGTAGGAGAATTGCTTGAA A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs555901853 Functional Loss SNV dbSNP153 33..33 33 - - - 38537 RMVar_ID_38537 Human_SNP_ID_315396214 A-to-I Human chr7 + 30429910 30429910 30429910 GGGCATGGTGGTGTGCACCTGTACTCCCAGCTACTCGGGAGACTGAGGTAGGAGAATTGCTTGAA GGGCATGGTGGTGTGCACCTGTACTCCCAGCTGCTCGGGAGACTGAGGTAGGAGAATTGCTTGAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs555901853 Functional Loss SNV dbSNP153 33..33 33 - - - 38538 RMVar_ID_38538 Human_SNP_ID_315404950 A-to-I Human chr7 - 30465412 30465412 30465412 ATGAAGCTCCTGCTAAATGGATCATGTTTGCTAGTGTTTTTTAGGCTGCAGAGAACAGGGGCACA ATGAAGCTCCTGCTAAATGGATCATGTTTGCTGGTGTTTTTTAGGCTGCAGAGAACAGGGGCACA T C NOD1 Ensembl:ENSG00000106100 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1050114755 Functional Loss SNV dbSNP153 33..33 33 - - - 38539 RMVar_ID_38539 Human_SNP_ID_315405192 A-to-I Human chr7 - 30466615 30466615 30466615 TCACCCAGGCTGGAGTACAGTGGTGTGATCATAGCTCACTGTAGCCTCGAACTCTGAACTCCTGG TCACCCAGGCTGGAGTACAGTGGTGTGATCATTGCTCACTGTAGCCTCGAACTCTGAACTCCTGG T A NOD1 Ensembl:ENSG00000106100 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459737119 Functional Loss SNV dbSNP153 33..33 33 - - - 38540 RMVar_ID_38540 Human_SNP_ID_315405195 A-to-I Human chr7 - 30466631 30466621 30466631 ACAGGGGTCTCACTTGTCACCCAGGCTGGAGTACAGTGGTGTGATCATAGCTCACTGTAGCCTCG ACAGGGGTCTCACTTGTCACCCAGGCTGGAGT__________GATCATAGCTCACTGTAGCCTCG CACACCACTGT C NOD1 Ensembl:ENSG00000106100 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1178227949 Functional Loss DEL dbSNP153 33..42 33 - - - Human_RBP_ID_3085590 38541 RMVar_ID_38541 Human_SNP_ID_315405196 A-to-I Human chr7 - 30466629 30466629 30466629 AGGGGTCTCACTTGTCACCCAGGCTGGAGTACAGTGGTGTGATCATAGCTCACTGTAGCCTCGAA AGGGGTCTCACTTGTCACCCAGGCTGGAGTACGGTGGTGTGATCATAGCTCACTGTAGCCTCGAA T C NOD1 Ensembl:ENSG00000106100 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1254561331 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3085590 38542 RMVar_ID_38542 Human_SNP_ID_315416059 A-to-I Human chr7 - 30510929 30510929 30510929 ATACAAAAATTAGCCAGATGTGTTGCAACTGTAGTCCCAGCTATTCAAGAAACTGAAGTGGGAAG ATACAAAAATTAGCCAGATGTGTTGCAACTGTGGTCCCAGCTATTCAAGAAACTGAAGTGGGAAG T C AC005154.5 Ensembl:ENSG00000281039 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941598979 Functional Loss SNV dbSNP153 33..33 33 - - - 38543 RMVar_ID_38543 Human_SNP_ID_315417432 A-to-I Human chr7 - 30517453 30517453 30517453 TTCTGTCACCCAGGCTGGAGTGCAGTGGCGCAATCTCGGCTCGCTGCAAGCTCTGCCTCCCGGAT TTCTGTCACCCAGGCTGGAGTGCAGTGGCGCAGTCTCGGCTCGCTGCAAGCTCTGCCTCCCGGAT T C GARS1-DT,AC005154.5 Ensembl:ENSG00000196295,Ensembl:ENSG00000281039 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1034316029 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_853520,Human_Splice_Rec_853524 38544 RMVar_ID_38544 Human_SNP_ID_315417619 A-to-I Human chr7 - 30518276 30518276 30518276 TTTTGTATTTTTTGTAGAGACTGGGTTTTGCCATGTTGCACAGGCTGGTCTTGAAGTCCTGAGCT TTTTGTATTTTTTGTAGAGACTGGGTTTTGCCGTGTTGCACAGGCTGGTCTTGAAGTCCTGAGCT T C GARS1-DT,AC005154.5 Ensembl:ENSG00000196295,Ensembl:ENSG00000281039 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984713221 Functional Loss SNV dbSNP153 33..33 33 - - - 38545 RMVar_ID_38545 Human_SNP_ID_315420507 A-to-I Human chr7 - 30532105 30532105 30532105 CTCCTGCCTCAGCCTCCCGGGTGGCTGAGATTACAGGCATCTGCCACCATGCCCAACTATTTTTT CTCCTGCCTCAGCCTCCCGGGTGGCTGAGATTGCAGGCATCTGCCACCATGCCCAACTATTTTTT T C GARS1-DT,AC005154.5 Ensembl:ENSG00000196295,Ensembl:ENSG00000281039 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1453090992 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_244350,RMVar_hsa_circ_355994,RMVar_hsa_circ_325997,RMVar_hsa_circ_244349 38546 RMVar_ID_38546 Human_SNP_ID_315426843 A-to-I Human chr7 - 30559144 30559144 30559144 GTTACCCAGGCTGGTCTTGAACTTCTGGGCTCAAGCCTTCTGCCTGCCCTGGCCTTCCAAAGCAT GTTACCCAGGCTGGTCTTGAACTTCTGGGCTCGAGCCTTCTGCCTGCCCTGGCCTTCCAAAGCAT T C GARS1-DT Ensembl:ENSG00000196295 lincRNA intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1056921091 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107346,RMVar_hsa_circ_268331,RMVar_hsa_circ_244352,RMVar_hsa_circ_284611,RMVar_hsa_circ_244351,RMVar_hsa_circ_244355,RMVar_hsa_circ_83766,RMVar_hsa_circ_244354 38547 RMVar_ID_38547 Human_SNP_ID_315426868 A-to-I Human chr7 - 30559237 30559237 30559237 CCCACCTCTCAGCCTCCCAAGCAGCTGGGACTATGGGTGCATGCCACCACACCCAGCTAATTTTT CCCACCTCTCAGCCTCCCAAGCAGCTGGGACTGTGGGTGCATGCCACCACACCCAGCTAATTTTT T C GARS1-DT Ensembl:ENSG00000196295 lincRNA intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1203321632 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107346,RMVar_hsa_circ_268331,RMVar_hsa_circ_244352,RMVar_hsa_circ_284611,RMVar_hsa_circ_244351,RMVar_hsa_circ_244355,RMVar_hsa_circ_83766,RMVar_hsa_circ_244354 38548 RMVar_ID_38548 Human_SNP_ID_315427075 A-to-I Human chr7 - 30560152 30560152 30560152 GGCTAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTAGCTGGGCATGGTGGCGGTT GGCTAACATGGTGAAACCCCGTCTCTACTAAATATACAAAAAATTAGCTGGGCATGGTGGCGGTT T A GARS1-DT Ensembl:ENSG00000196295 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1040983141 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107346,RMVar_hsa_circ_268331,RMVar_hsa_circ_244352,RMVar_hsa_circ_284611,RMVar_hsa_circ_244351,RMVar_hsa_circ_244355,RMVar_hsa_circ_83766,RMVar_hsa_circ_244354 38549 RMVar_ID_38549 Human_SNP_ID_315427096 A-to-I Human chr7 - 30560241 30560241 30560241 GGCCGGGTGTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGAAGATCTTG GGCCGGGTGTGGTGGCTCACACCTGTAATCCCGGCACTTTGGGAGGCCGAGGCAGGAAGATCTTG T C GARS1-DT Ensembl:ENSG00000196295 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs531725042 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107346,RMVar_hsa_circ_268331,RMVar_hsa_circ_244352,RMVar_hsa_circ_284611,RMVar_hsa_circ_244351,RMVar_hsa_circ_244355,RMVar_hsa_circ_83766,RMVar_hsa_circ_244354 38550 RMVar_ID_38550 Human_SNP_ID_315427138 A-to-I Human chr7 - 30560409 30560409 30560409 AAACATAAAAAATTAACCAGGTGTGGTAGCACATGCCTGTGGTCTCAGCAACTTGGGAGGCTGAG AAACATAAAAAATTAACCAGGTGTGGTAGCACGTGCCTGTGGTCTCAGCAACTTGGGAGGCTGAG T C GARS1-DT Ensembl:ENSG00000196295 lincRNA intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs548418082 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27112762 RMVar_hsa_circ_107346,RMVar_hsa_circ_268331,RMVar_hsa_circ_244352,RMVar_hsa_circ_284611,RMVar_hsa_circ_244351,RMVar_hsa_circ_244355,RMVar_hsa_circ_83766,RMVar_hsa_circ_244354 38551 RMVar_ID_38551 Human_SNP_ID_315427145 A-to-I Human chr7 - 30560426 30560426 30560426 AATCCCATCTCTAACAAAAACATAAAAAATTAACCAGGTGTGGTAGCACATGCCTGTGGTCTCAG AATCCCATCTCTAACAAAAACATAAAAAATTACCCAGGTGTGGTAGCACATGCCTGTGGTCTCAG T G GARS1-DT Ensembl:ENSG00000196295 lincRNA intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs953088305 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107346,RMVar_hsa_circ_268331,RMVar_hsa_circ_244352,RMVar_hsa_circ_284611,RMVar_hsa_circ_244351,RMVar_hsa_circ_244355,RMVar_hsa_circ_83766,RMVar_hsa_circ_244354 38552 RMVar_ID_38552 Human_SNP_ID_315427248 A-to-I Human chr7 - 30560981 30560981 30560981 ATTGGCCAGGCTGGTCTTGAACTCCTGACCTCAGGTGATCAGCCTGTCTCGGCCTCCCACACACA ATTGGCCAGGCTGGTCTTGAACTCCTGACCTCGGGTGATCAGCCTGTCTCGGCCTCCCACACACA T C GARS1-DT Ensembl:ENSG00000196295 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1360423923 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5223074 RMVar_hsa_circ_107346,RMVar_hsa_circ_268331,RMVar_hsa_circ_244352,RMVar_hsa_circ_284611,RMVar_hsa_circ_244351,RMVar_hsa_circ_244355,RMVar_hsa_circ_83766,RMVar_hsa_circ_244354 38553 RMVar_ID_38553 Human_SNP_ID_315427261 A-to-I Human chr7 - 30561041 30561041 30561041 GGCACGTGCTACCACGCCCAGCTAATTTTTGTATTTTTGGTAGAGACGTGGTTTCATCATATTGG GGCACGTGCTACCACGCCCAGCTAATTTTTGTGTTTTTGGTAGAGACGTGGTTTCATCATATTGG T C GARS1-DT Ensembl:ENSG00000196295 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1412750054 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107346,RMVar_hsa_circ_268331,RMVar_hsa_circ_244352,RMVar_hsa_circ_284611,RMVar_hsa_circ_244351,RMVar_hsa_circ_244355,RMVar_hsa_circ_83766,RMVar_hsa_circ_244354 38554 RMVar_ID_38554 Human_SNP_ID_315428334 A-to-I Human chr7 - 30565355 30565355 30565355 CTCCTGCCTCAGCCTCCCGAGTAGCCCGGACTATAGGGGCCTGCCACCATGTCCAGCTAATTTTT CTCCTGCCTCAGCCTCCCGAGTAGCCCGGACTGTAGGGGCCTGCCACCATGTCCAGCTAATTTTT T C GARS1-DT Ensembl:ENSG00000196295 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904393515 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107346,RMVar_hsa_circ_244351,RMVar_hsa_circ_244355 38555 RMVar_ID_38555 Human_SNP_ID_315443209 A-to-I Human chr7 + 30627817 30627817 30627817 TAAACAAATACAAACCATGTAATACTTTTTGCATGTAGGAATTGTTTTTGTGAATTTTGCCAGCT TAAACAAATACAAACCATGTAATACTTTTTGCGTGTAGGAATTGTTTTTGTGAATTTTGCCAGCT A G GARS1 Ensembl:ENSG00000106105 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2709778 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_4349,GWAS_ID_4350 RMVar_hsa_circ_69682,RMVar_hsa_circ_11800,RMVar_hsa_circ_84451,RMVar_hsa_circ_122558,RMVar_hsa_circ_244362,RMVar_hsa_circ_244363,RMVar_hsa_circ_33073,RMVar_hsa_circ_93460,RMVar_hsa_circ_244371,RMVar_hsa_circ_96258,RMVar_hsa_circ_93772,RMVar_hsa_circ_244373,RMVar_hsa_circ_43965,RMVar_hsa_circ_244374,RMVar_hsa_circ_244375,RMVar_hsa_circ_76799,RMVar_hsa_circ_99592,RMVar_hsa_circ_98272,RMVar_hsa_circ_81268,RMVar_hsa_circ_244379,RMVar_hsa_circ_244380,RMVar_hsa_circ_244377,RMVar_hsa_circ_244378 38556 RMVar_ID_38556 Human_SNP_ID_315443341 A-to-I Human chr7 + 30628359 30628359 30628359 CGCACCTGCCACCATACCCAGTTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGG CGCACCTGCCACCATACCCAGTTAATTTTTGTGTTTTTAGTAGAGACGGGGTTTCACCATGTTGG A G GARS1 Ensembl:ENSG00000106105 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs544585777 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69682,RMVar_hsa_circ_11800,RMVar_hsa_circ_84451,RMVar_hsa_circ_122558,RMVar_hsa_circ_244362,RMVar_hsa_circ_244363,RMVar_hsa_circ_33073,RMVar_hsa_circ_93460,RMVar_hsa_circ_244371,RMVar_hsa_circ_96258,RMVar_hsa_circ_93772,RMVar_hsa_circ_244373,RMVar_hsa_circ_43965,RMVar_hsa_circ_244374,RMVar_hsa_circ_244375,RMVar_hsa_circ_76799,RMVar_hsa_circ_99592,RMVar_hsa_circ_98272,RMVar_hsa_circ_81268,RMVar_hsa_circ_244379,RMVar_hsa_circ_244380,RMVar_hsa_circ_244377,RMVar_hsa_circ_244378 38557 RMVar_ID_38557 Human_SNP_ID_315483392 A-to-I Human chr7 + 30786566 30786566 30786566 GGAGGATTGCTTGAACCTGGGAGGTTGAGGCTACAGTGAGCTGTGATCATGTGACTGTACTCTGG GGAGGATTGCTTGAACCTGGGAGGTTGAGGCTGCAGTGAGCTGTGATCATGTGACTGTACTCTGG A G MINDY4,INMT-MINDY4 Ensembl:ENSG00000106125,Ensembl:ENSG00000254959 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251158588 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_345394,RMVar_hsa_circ_367436,RMVar_hsa_circ_244389,RMVar_hsa_circ_244390,RMVar_hsa_circ_343033 38558 RMVar_ID_38558 Human_SNP_ID_315564672 A-to-I Human chr7 + 31108239 31108239 31108239 AATGTTTCTGGAGAGGCTTTCAGAGTGGCTGGAAAAGGCTCTTGTTGCTGTAATTTAGAGAGGAG AATGTTTCTGGAGAGGCTTTCAGAGTGGCTGGGAAAGGCTCTTGTTGCTGTAATTTAGAGAGGAG A G ADCYAP1R1 Ensembl:ENSG00000078549 Protein coding 3'UTR GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1024745450 Functional Loss SNV dbSNP153 33..33 33 - - - 38559 RMVar_ID_38559 Human_SNP_ID_315899609 A-to-I Human chr7 - 32472079 32472079 32472079 CCCTTTGCAGTGTCATAGATACCAAAGTAGGCAGCTCGGTAGATGATAATACCCTGCACAGACAC CCCTTTGCAGTGTCATAGATACCAAAGTAGGCGGCTCGGTAGATGATAATACCCTGCACAGACAC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879193920 Functional Loss SNV dbSNP153 33..33 33 - - - 38560 RMVar_ID_38560 Human_SNP_ID_315899610 A-to-I Human chr7 - 32472079 32472079 32472079 CCCTTTGCAGTGTCATAGATACCAAAGTAGGCAGCTCGGTAGATGATAATACCCTGCACAGACAC CCCTTTGCAGTGTCATAGATACCAAAGTAGGCCGCTCGGTAGATGATAATACCCTGCACAGACAC T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879193920 Functional Loss SNV dbSNP153 33..33 33 - - - 38561 RMVar_ID_38561 Human_SNP_ID_315899613 A-to-I Human chr7 - 32472088 32472088 32472088 GGAAGCATTCCCTTTGCAGTGTCATAGATACCAAAGTAGGCAGCTCGGTAGATGATAATACCCTG GGAAGCATTCCCTTTGCAGTGTCATAGATACCGAAGTAGGCAGCTCGGTAGATGATAATACCCTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879119617 Functional Loss SNV dbSNP153 33..33 33 - - - 38562 RMVar_ID_38562 Human_SNP_ID_315906541 A-to-I Human chr7 + 32498374 32498374 32498374 GGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCATGCACCACCGTA GGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCCAGTAGCTGGGATTACAGGCATGCACCACCGTA A C AVL9 Ensembl:ENSG00000105778 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs535460704 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_244420,RMVar_hsa_circ_113624 38563 RMVar_ID_38563 Human_SNP_ID_315913514 A-to-I Human chr7 + 32524376 32524376 32524376 CGTCTCTACTAAAATACAAAAATTAGCCTGGCATGATGGCAGGTGGCTGTAATCCCAGCTACTCG CGTCTCTACTAAAATACAAAAATTAGCCTGGCGTGATGGCAGGTGGCTGTAATCCCAGCTACTCG A G AVL9 Ensembl:ENSG00000105778 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs981324525 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_244420,RMVar_hsa_circ_113624 38564 RMVar_ID_38564 Human_SNP_ID_315913530 A-to-I Human chr7 + 32524460 32524460 32524460 TTGCTTGAACTCAGGAGACAGTGGTTGCAGTGAACCGAGATCATGCTACTGCACTCCTCCCTGGG TTGCTTGAACTCAGGAGACAGTGGTTGCAGTGTACCGAGATCATGCTACTGCACTCCTCCCTGGG A T AVL9 Ensembl:ENSG00000105778 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1451901332 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16140263 RMVar_hsa_circ_244420,RMVar_hsa_circ_113624 38565 RMVar_ID_38565 Human_SNP_ID_315913532 A-to-I Human chr7 + 32524470 32524470 32524470 TCAGGAGACAGTGGTTGCAGTGAACCGAGATCATGCTACTGCACTCCTCCCTGGGCGGCTGAGCG TCAGGAGACAGTGGTTGCAGTGAACCGAGATCGTGCTACTGCACTCCTCCCTGGGCGGCTGAGCG A G AVL9 Ensembl:ENSG00000105778 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs533197756 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16140263 RMVar_hsa_circ_244420,RMVar_hsa_circ_113624 38566 RMVar_ID_38566 Human_SNP_ID_315916644 A-to-I Human chr7 + 32537567 32537567 32537567 TCACTGCAACCACCACCACCTGAGTTCAAGTGATTCTCCTGCCTCAGCCTCCTGAGTAGTTGGGA TCACTGCAACCACCACCACCTGAGTTCAAGTGTTTCTCCTGCCTCAGCCTCCTGAGTAGTTGGGA A T AVL9 Ensembl:ENSG00000105778 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs956678153 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_244420,RMVar_hsa_circ_113624,RMVar_hsa_circ_244421 38567 RMVar_ID_38567 Human_SNP_ID_315917056 A-to-I Human chr7 + 32539245 32539245 32539245 TGCACTCCAGCCTGGGCAACGAGCGAAACTCCATCTCAAAAAAAAAGAAAAGGAAAAGAAAAGTG TGCACTCCAGCCTGGGCAACGAGCGAAACTCCGTCTCAAAAAAAAAGAAAAGGAAAAGAAAAGTG A G AVL9 Ensembl:ENSG00000105778 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1248574114 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_244420,RMVar_hsa_circ_113624,RMVar_hsa_circ_244421 38568 RMVar_ID_38568 Human_SNP_ID_315921606 A-to-I Human chr7 + 32556852 32556852 32556852 CAGCGGTGTGATCATGGCTCACTGCAACCTCTAACTCCCAGGCTCAAGCAATTCTTCCACCTCAG CAGCGGTGTGATCATGGCTCACTGCAACCTCTGACTCCCAGGCTCAAGCAATTCTTCCACCTCAG A G AVL9 Ensembl:ENSG00000105778 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1014533993 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_982,RMVar_hsa_circ_318834,RMVar_hsa_circ_270285,RMVar_hsa_circ_44587,RMVar_hsa_circ_89047,RMVar_hsa_circ_3570,RMVar_hsa_circ_50767,RMVar_hsa_circ_244429,RMVar_hsa_circ_244430,RMVar_hsa_circ_244428,RMVar_hsa_circ_288380,RMVar_hsa_circ_273500,RMVar_hsa_circ_27169,RMVar_hsa_circ_38227,RMVar_hsa_circ_20748,RMVar_hsa_circ_244438,RMVar_hsa_circ_244431,RMVar_hsa_circ_244432,RMVar_hsa_circ_334955,RMVar_hsa_circ_11245,RMVar_hsa_circ_355173,RMVar_hsa_circ_372670,RMVar_hsa_circ_331070,RMVar_hsa_circ_68933,RMVar_hsa_circ_244439,RMVar_hsa_circ_244440,RMVar_hsa_circ_117333,RMVar_hsa_circ_244441 38569 RMVar_ID_38569 Human_SNP_ID_315923810 A-to-I Human chr7 + 32565798 32565798 32565798 GGGAGGCCGAGGCGGGCACATCATCTGAGGTCAAGAGATCAAGACCATCCAGGCCAACATGGTGA GGGAGGCCGAGGCGGGCACATCATCTGAGGTCCAGAGATCAAGACCATCCAGGCCAACATGGTGA A C AVL9 Ensembl:ENSG00000105778 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs184354307 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19482,RMVar_hsa_circ_982,RMVar_hsa_circ_44587,RMVar_hsa_circ_89047,RMVar_hsa_circ_3570,RMVar_hsa_circ_50767,RMVar_hsa_circ_244429,RMVar_hsa_circ_244430,RMVar_hsa_circ_273500,RMVar_hsa_circ_38227,RMVar_hsa_circ_20748,RMVar_hsa_circ_244431,RMVar_hsa_circ_372670,RMVar_hsa_circ_331070,RMVar_hsa_circ_244439,RMVar_hsa_circ_244440,RMVar_hsa_circ_117333,RMVar_hsa_circ_269620,RMVar_hsa_circ_315753,RMVar_hsa_circ_244441,RMVar_hsa_circ_322192,RMVar_hsa_circ_244444,RMVar_hsa_circ_265469 38570 RMVar_ID_38570 Human_SNP_ID_315929134 A-to-I Human chr7 - 32583673 32583673 32583673 AATTAAAAATTTAAAAAAATGTTTTTTGAGACAGCGTCTTACTCTGTCGCCCAGGCTGGAGTGCA AATTAAAAATTTAAAAAAATGTTTTTTGAGACCGCGTCTTACTCTGTCGCCCAGGCTGGAGTGCA T G DPY19L1P1 Ensembl:ENSG00000229358 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs961105608 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_244450,RMVar_hsa_circ_126404 38571 RMVar_ID_38571 Human_SNP_ID_315964437 A-to-I Human chr7 - 32716543 32716543 32716543 ACCTTGTCTCTTCTAAAATACAAAAGTTAGCCAGGCATGGTGGTGTGCATCTGTAATCCCAGCTA ACCTTGTCTCTTCTAAAATACAAAAGTTAGCCGGGCATGGTGGTGTGCATCTGTAATCCCAGCTA T C DPY19L1P1 Ensembl:ENSG00000229358 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1271750618 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7582,RMVar_hsa_circ_365450,RMVar_hsa_circ_56625,RMVar_hsa_circ_244457,RMVar_hsa_circ_301882,RMVar_hsa_circ_28777,RMVar_hsa_circ_244459,RMVar_hsa_circ_372849,RMVar_hsa_circ_244464,RMVar_hsa_circ_295568,RMVar_hsa_circ_49450,RMVar_hsa_circ_47040,RMVar_hsa_circ_313117,RMVar_hsa_circ_362033 38572 RMVar_ID_38572 Human_SNP_ID_315964438 A-to-I Human chr7 - 32716547 32716547 32716547 TGAAACCTTGTCTCTTCTAAAATACAAAAGTTAGCCAGGCATGGTGGTGTGCATCTGTAATCCCA TGAAACCTTGTCTCTTCTAAAATACAAAAGTTGGCCAGGCATGGTGGTGTGCATCTGTAATCCCA T C DPY19L1P1 Ensembl:ENSG00000229358 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1362342543 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7582,RMVar_hsa_circ_365450,RMVar_hsa_circ_56625,RMVar_hsa_circ_244457,RMVar_hsa_circ_301882,RMVar_hsa_circ_28777,RMVar_hsa_circ_244459,RMVar_hsa_circ_372849,RMVar_hsa_circ_244464,RMVar_hsa_circ_295568,RMVar_hsa_circ_49450,RMVar_hsa_circ_47040,RMVar_hsa_circ_313117,RMVar_hsa_circ_362033 38573 RMVar_ID_38573 Human_SNP_ID_315992521 A-to-I Human chr7 + 32833315 32833315 32833315 CTTTTCTGGTAGAGACAAAGGTGAAGCGTTTTATCTGTGAACCCAAAACTCCGGCGCCGGTCACA CTTTTCTGGTAGAGACAAAGGTGAAGCGTTTTGTCTGTGAACCCAAAACTCCGGCGCCGGTCACA A G DPY19L1P2 Ensembl:ENSG00000231952 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs547960194 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19139724 Human_miRNA_ID_2913756,Human_miRNA_ID_2913757 RMVar_hsa_circ_89047,RMVar_hsa_circ_244430,RMVar_hsa_circ_41704,RMVar_hsa_circ_90274,RMVar_hsa_circ_244470,RMVar_hsa_circ_244468,RMVar_hsa_circ_244469 38574 RMVar_ID_38574 Human_SNP_ID_315992956 A-to-I Human chr7 + 32834778 32834778 32834778 CGGACTGTTCAACTCCCCTGGCAGCCACTTCCAGAGCCCCTGGAACTCTGGCCCAAGGCTCTCTG CGGACTGTTCAACTCCCCTGGCAGCCACTTCCGGAGCCCCTGGAACTCTGGCCCAAGGCTCTCTG A G DPY19L1P2 Ensembl:ENSG00000231952 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900358377 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2661726,Human_miRNA_ID_2661727,Human_miRNA_ID_3068582,Human_miRNA_ID_3068583 RMVar_hsa_circ_89047,RMVar_hsa_circ_244430,RMVar_hsa_circ_41704,RMVar_hsa_circ_90274,RMVar_hsa_circ_244470,RMVar_hsa_circ_244468,RMVar_hsa_circ_244469 38575 RMVar_ID_38575 Human_SNP_ID_316005023 A-to-I Human chr7 - 32883262 32883262 32883262 AGCTTGAAGCAGCCTCAGCCTCCAGAGTAGCTAGTATTACAGGCATGAGCCACCATACCCGACTA AGCTTGAAGCAGCCTCAGCCTCCAGAGTAGCTGGTATTACAGGCATGAGCCACCATACCCGACTA T C KBTBD2 Ensembl:ENSG00000170852 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1191145499 Functional Loss SNV dbSNP153 33..33 33 - - - 38576 RMVar_ID_38576 Human_SNP_ID_316039123 A-to-I Human chr7 - 33015532 33015532 33015532 TTTTTTTGAGACAAGCCTCTGTTACCGAGGCTAGAGTGTAGTGATGCAATCACATCTCACTGCAG TTTTTTTGAGACAAGCCTCTGTTACCGAGGCTGGAGTGTAGTGATGCAATCACATCTCACTGCAG T C NT5C3A Ensembl:ENSG00000122643 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1483897870 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16141615 38577 RMVar_ID_38577 Human_SNP_ID_316048886 A-to-I Human chr7 - 33055140 33055140 33055140 TTGTATTTTTAGGAGAGATGAGGTTTCTCCATATTTGCCAGGCTGGTCTTGAACTCCTGACCTCA TTGTATTTTTAGGAGAGATGAGGTTTCTCCATGTTTGCCAGGCTGGTCTTGAACTCCTGACCTCA T C NT5C3A Ensembl:ENSG00000122643 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs550213269 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26099933 38578 RMVar_ID_38578 Human_SNP_ID_316333300 A-to-I Human chr7 + 34250462 34250462 34250462 TGATCTCAGATGGCAGCAAGCTAAGGCAGGATAGAATGAATGGCTTGAACACAAGGAGAATGTGG TGATCTCAGATGGCAGCAAGCTAAGGCAGGATGGAATGAATGGCTTGAACACAAGGAGAATGTGG A G AC009262.1 Ensembl:ENSG00000236212 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs375275442 Functional Loss SNV dbSNP153 33..33 33 - - - 38579 RMVar_ID_38579 Human_SNP_ID_316333749 A-to-I Human chr7 + 34251933 34251933 34251933 CTTAAGAGAATCCACCTTAAATTAGCGCCTTTACCATTTTCCAGGTAATGCAAGGAGCTCACAAC CTTAAGAGAATCCACCTTAAATTAGCGCCTTTGCCATTTTCCAGGTAATGCAAGGAGCTCACAAC A G AC009262.1 Ensembl:ENSG00000236212 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1196105155 Functional Loss SNV dbSNP153 33..33 33 - - - 38580 RMVar_ID_38580 Human_SNP_ID_316333754 A-to-I Human chr7 + 34251963 34251963 34251963 TTACCATTTTCCAGGTAATGCAAGGAGCTCACAACTCTTTGATCCTTTCTGACATTTTGTGCTAT TTACCATTTTCCAGGTAATGCAAGGAGCTCACGACTCTTTGATCCTTTCTGACATTTTGTGCTAT A G AC009262.1 Ensembl:ENSG00000236212 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1337312243 Functional Loss SNV dbSNP153 33..33 33 - - - 38581 RMVar_ID_38581 Human_SNP_ID_316333769 A-to-I Human chr7 + 34252055 34252055 34252055 TATTTAAGCCCTCACAAGATATTATTATTATTATCACTGAAAATATATTTATTCAATCTGCCCAC TATTTAAGCCCTCACAAGATATTATTATTATTGTCACTGAAAATATATTTATTCAATCTGCCCAC A G AC009262.1 Ensembl:ENSG00000236212 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1300214784 Functional Loss SNV dbSNP153 33..33 33 - - - 38582 RMVar_ID_38582 Human_SNP_ID_316452785 A-to-I Human chr7 - 34750641 34750641 34750641 TTCTTTTTTGTCAGTTATGGGCAAGCTACAACATGGGGCCAAGCCTGAGGGCAAGGCTATAATAG TTCTTTTTTGTCAGTTATGGGCAAGCTACAACGTGGGGCCAAGCCTGAGGGCAAGGCTATAATAG T C NPSR1-AS1,NCAPD2P1 Ensembl:ENSG00000197085,Ensembl:ENSG00000230356 lincRNA,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1179007244 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11856 38583 RMVar_ID_38583 Human_SNP_ID_316452787 A-to-I Human chr7 - 34750657 34750657 34750657 ATGAGTCCATCTTCAGTTCTTTTTTGTCAGTTATGGGCAAGCTACAACATGGGGCCAAGCCTGAG ATGAGTCCATCTTCAGTTCTTTTTTGTCAGTTGTGGGCAAGCTACAACATGGGGCCAAGCCTGAG T C NPSR1-AS1,NCAPD2P1 Ensembl:ENSG00000197085,Ensembl:ENSG00000230356 lincRNA,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs186962582 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16272982 RMVar_hsa_circ_11856 38584 RMVar_ID_38584 Human_SNP_ID_316556820 A-to-I Human chr7 - 35185910 35185910 35185910 GAAAAGTCGGCCCTAGGCGGCGGGAAACTGCCAGGGGGCGCCAGGAGGTCCTCCCCGGGGAGGAT GAAAAGTCGGCCCTAGGCGGCGGGAAACTGCCGGGGGGCGCCAGGAGGTCCTCCCCGGGGAGGAT T C DPY19L2P1 Ensembl:ENSG00000189212 Pseudogene exon GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1345355234 Functional Loss SNV dbSNP153 33..33 33 - - - 38585 RMVar_ID_38585 Human_SNP_ID_316674971 A-to-I Human chr7 - 35687008 35687008 35687008 TCGTCTGGGCTGGAGTGCAGTGGCGTGATCTCAGCTCACTGCAACCTCTGCCTCCTGGGTTCAAG TCGTCTGGGCTGGAGTGCAGTGGCGTGATCTCGGCTCACTGCAACCTCTGCCTCCTGGGTTCAAG T C HERPUD2 Ensembl:ENSG00000122557 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1316760236 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112727,RMVar_hsa_circ_111768,RMVar_hsa_circ_244609,RMVar_hsa_circ_378019,RMVar_hsa_circ_244614 38586 RMVar_ID_38586 Human_SNP_ID_316702924 A-to-I Human chr7 + 35811899 35811899 35811899 CAAAAATTAGCTTCCTGCAGTGGCAGGTGCCTATAATCCCAGCTACTCGGGAGGCTGAGGCAGGA CAAAAATTAGCTTCCTGCAGTGGCAGGTGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGA A G SEPTIN7 Ensembl:ENSG00000122545 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1212175421 Functional Loss SNV dbSNP153 33..33 33 - - - 38587 RMVar_ID_38587 Human_SNP_ID_316702959 A-to-I Human chr7 + 35812006 35812006 35812006 AAAATTAGCCAGACATGGTGGTTGGTGCCTGTAATCCCAGTTACTCAGGAGGCTGAGGCAGGAGA AAAATTAGCCAGACATGGTGGTTGGTGCCTGTGATCCCAGTTACTCAGGAGGCTGAGGCAGGAGA A G SEPTIN7 Ensembl:ENSG00000122545 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1040143717 Functional Loss SNV dbSNP153 33..33 33 - - - 38588 RMVar_ID_38588 Human_SNP_ID_316720391 A-to-I Human chr7 + 35887464 35887464 35887464 CTCCACCCAGGTTCAAGTAATTCTCCTGCCTCAGCTTCCTGAGTAGCTGGGATTATAGGCATGCA CTCCACCCAGGTTCAAGTAATTCTCCTGCCTCCGCTTCCTGAGTAGCTGGGATTATAGGCATGCA A C SEPTIN7 Ensembl:ENSG00000122545 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1409873652 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_341210,RMVar_hsa_circ_301680,RMVar_hsa_circ_337302,RMVar_hsa_circ_244629 38589 RMVar_ID_38589 Human_SNP_ID_316720688 A-to-I Human chr7 + 35888618 35888618 35888618 AAGGTGGGAGAATTGCTTGAGCTCAGGAGTTCAAGACTGGCCTGGGCAACATGGTGAAACCTCGT AAGGTGGGAGAATTGCTTGAGCTCAGGAGTTCCAGACTGGCCTGGGCAACATGGTGAAACCTCGT A C SEPTIN7 Ensembl:ENSG00000122545 Protein coding intron GSE38233;GSE107867 cultured B-cells;ASD brains,Fragile X samples from NIH NeuroBioBank - 24183664,30559470 RNA-Seq:(High) rs1432200534 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_341210,RMVar_hsa_circ_301680,RMVar_hsa_circ_337302,RMVar_hsa_circ_244629 38590 RMVar_ID_38590 Human_SNP_ID_316720698 A-to-I Human chr7 + 35888658 35888658 35888658 CCTGGGCAACATGGTGAAACCTCGTCCCTACTAAAAATACAAGAAATAGTCGGGCGTGGTGGTGC CCTGGGCAACATGGTGAAACCTCGTCCCTACTGAAAATACAAGAAATAGTCGGGCGTGGTGGTGC A G SEPTIN7 Ensembl:ENSG00000122545 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1368913972 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_341210,RMVar_hsa_circ_301680,RMVar_hsa_circ_337302,RMVar_hsa_circ_244629 38591 RMVar_ID_38591 Human_SNP_ID_316720700 A-to-I Human chr7 + 35888664 35888664 35888664 CAACATGGTGAAACCTCGTCCCTACTAAAAATACAAGAAATAGTCGGGCGTGGTGGTGCATGCCT CAACATGGTGAAACCTCGTCCCTACTAAAAATGCAAGAAATAGTCGGGCGTGGTGGTGCATGCCT A G SEPTIN7 Ensembl:ENSG00000122545 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1462547513 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26101701 RMVar_hsa_circ_341210,RMVar_hsa_circ_301680,RMVar_hsa_circ_337302,RMVar_hsa_circ_244629 38592 RMVar_ID_38592 Human_SNP_ID_316720717 A-to-I Human chr7 + 35888709 35888709 35888709 GGGCGTGGTGGTGCATGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGTGGGAGGATGGTTTGAG GGGCGTGGTGGTGCATGCCTGTAGTCCCAGCTGCTCAGGAGGCTGAGGTGGGAGGATGGTTTGAG A G SEPTIN7 Ensembl:ENSG00000122545 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1022990842 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_341210,RMVar_hsa_circ_301680,RMVar_hsa_circ_337302,RMVar_hsa_circ_244629 38593 RMVar_ID_38593 Human_SNP_ID_316720733 A-to-I Human chr7 + 35888777 35888777 35888777 GAAAGGCAGAGATTGTAGTGAGCTGAGATCGTACCACTGCATTCCATCCAGCCTGGGCAACAGAG GAAAGGCAGAGATTGTAGTGAGCTGAGATCGTTCCACTGCATTCCATCCAGCCTGGGCAACAGAG A T SEPTIN7 Ensembl:ENSG00000122545 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs995369379 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26101705 RMVar_hsa_circ_341210,RMVar_hsa_circ_301680,RMVar_hsa_circ_337302,RMVar_hsa_circ_244629 38594 RMVar_ID_38594 Human_SNP_ID_316721047 A-to-I Human chr7 + 35889718 35889718 35889718 GGTGCTTGCCACCACGCCCAACTGATTTTTGTATTTTTAGTAGAGATGGGGTTCCACCATGTTGG GGTGCTTGCCACCACGCCCAACTGATTTTTGTGTTTTTAGTAGAGATGGGGTTCCACCATGTTGG A G SEPTIN7 Ensembl:ENSG00000122545 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1393221013 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_341210,RMVar_hsa_circ_301680,RMVar_hsa_circ_337302,RMVar_hsa_circ_244629 38595 RMVar_ID_38595 Human_SNP_ID_316814087 A-to-I Human chr7 + 36268245 36268245 36268245 GTGATCTCGGCTCACTGCAACCTCTGCCTCGCAGGTTCAGGTGATTCTCTTGCCTCAGCCTCCCG GTGATCTCGGCTCACTGCAACCTCTGCCTCGCGGGTTCAGGTGATTCTCTTGCCTCAGCCTCCCG A G EEPD1 Ensembl:ENSG00000122547 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1270070409 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79699,RMVar_hsa_circ_244630 38596 RMVar_ID_38596 Human_SNP_ID_316814127 A-to-I Human chr7 + 36268433 36268433 36268433 CACCCACTTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCTTACCCAGCTGCTTGCT CACCCACTTCGGCCTCCCAAAGTGCTGGGATTGCAGGCATGAGCCACCTTACCCAGCTGCTTGCT A G EEPD1 Ensembl:ENSG00000122547 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1182301587 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79699,RMVar_hsa_circ_244630 38597 RMVar_ID_38597 Human_SNP_ID_316833960 A-to-I Human chr7 - 36350679 36350679 36350679 AAATTATCTGGGCATGGTGGCGCATGCCTGTAATCCCAGCTACTTCGGAGGCTGAGATGAGGATT AAATTATCTGGGCATGGTGGCGCATGCCTGTACTCCCAGCTACTTCGGAGGCTGAGATGAGGATT T G KIAA0895 Ensembl:ENSG00000164542 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1163272455 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35116,RMVar_hsa_circ_335829 38598 RMVar_ID_38598 Human_SNP_ID_316848555 A-to-I Human chr7 + 36412562 36412562 36412562 GTTGGTCAGGCTGGTCTCGAACTCGTGACCTCAGGTGATCCGCCCGCCTCAGCCTCTCAAAGTGC GTTGGTCAGGCTGGTCTCGAACTCGTGACCTCTGGTGATCCGCCCGCCTCAGCCTCTCAAAGTGC A T ANLN Ensembl:ENSG00000011426 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1212795139 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 38599 RMVar_ID_38599 Human_SNP_ID_316853578 A-to-I Human chr7 + 36432881 36432881 36432881 GAAATACTGTTACACTGCTTCATGTAACTTACAATATGAACCTCACAACAGTATAGTTCATTTTC GAAATACTGTTACACTGCTTCATGTAACTTACGATATGAACCTCACAACAGTATAGTTCATTTTC A G ANLN Ensembl:ENSG00000011426 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs527652037 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7736161,Human_RBP_ID_16147851,Human_RBP_ID_24213873 RMVar_hsa_circ_122113,RMVar_hsa_circ_111988,RMVar_hsa_circ_244652,RMVar_hsa_circ_92065,RMVar_hsa_circ_244653,RMVar_hsa_circ_244651,RMVar_hsa_circ_336842,RMVar_hsa_circ_70742,RMVar_hsa_circ_94353,RMVar_hsa_circ_244656,RMVar_hsa_circ_244658,RMVar_hsa_circ_20522,RMVar_hsa_circ_309686,RMVar_hsa_circ_336357 38600 RMVar_ID_38600 Human_SNP_ID_316880492 A-to-I Human chr7 - 36538152 36538152 36538152 GTGGTGGCACACACCTGTGATCCCAACTACTCAGGAGACTGAAGCAGGAGAATCGCTTGAACCCA GTGGTGGCACACACCTGTGATCCCAACTACTCGGGAGACTGAAGCAGGAGAATCGCTTGAACCCA T C AOAH Ensembl:ENSG00000136250 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1401339784 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70987 38601 RMVar_ID_38601 Human_SNP_ID_317213774 A-to-I Human chr7 + 37930704 37930704 37930704 TCTCCTTAAGGAGTTAGGAAATGAAGCTTGGGAATCCACTTCTCGGACATCAGAACACAGTTCCT TCTCCTTAAGGAGTTAGGAAATGAAGCTTGGGTATCCACTTCTCGGACATCAGAACACAGTTCCT A T EPDR1 Ensembl:ENSG00000086289 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1036011927 Functional Loss SNV dbSNP153 33..33 33 - - - 38602 RMVar_ID_38602 Human_SNP_ID_317311734 A-to-I Human chr7 - 38311810 38311810 38311810 GCTGGCCCCCCAGTCTGCACCAACCTCTTCAGAGCAGGGAGCTCAGACCATGGTTGTACTTGCAC GCTGGCCCCCCAGTCTGCACCAACCTCTTCAGGGCAGGGAGCTCAGACCATGGTTGTACTTGCAC T C lnc-AMPH-10,lnc-AMPH-10:2,lnc-AMPH-10:3,lnc-AMPH-10:4,lnc-AMPH-10:5,lnc-AMPH-10:6 RNACentral:URS00008BEDF4,RNACentral:URS00008B2B38,RNACentral:URS00008BD716,RNACentral:URS00008B5A0D,RNACentral:URS00008B7621,RNACentral:URS00008BAE5D lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1198315259 Functional Loss SNV dbSNP153 33..33 33 - - - 38603 RMVar_ID_38603 Human_SNP_ID_317311737 A-to-I Human chr7 - 38311821 38311821 38311821 GTGGGTGCAGGGCTGGCCCCCCAGTCTGCACCAACCTCTTCAGAGCAGGGAGCTCAGACCATGGT GTGGGTGCAGGGCTGGCCCCCCAGTCTGCACCGACCTCTTCAGAGCAGGGAGCTCAGACCATGGT T C lnc-AMPH-10,lnc-AMPH-10:2,lnc-AMPH-10:3,lnc-AMPH-10:4,lnc-AMPH-10:5,lnc-AMPH-10:6 RNACentral:URS00008BEDF4,RNACentral:URS00008B2B38,RNACentral:URS00008BD716,RNACentral:URS00008B5A0D,RNACentral:URS00008B7621,RNACentral:URS00008BAE5D lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1201417871 Functional Loss SNV dbSNP153 33..33 33 - - - 38604 RMVar_ID_38604 Human_SNP_ID_317413881 A-to-I Human chr7 - 38723460 38723460 38723462 TCGGCCTTCCGAAGTGTTAGGATTACAGGCGTAAGTCACCATGCCCAGCCAAGAAAGCTATTCTT TCGGCCTTCCGAAGTGTTAGGATTACAGGCATGAGTCACCATGCCCAGCCAAGAAAGCTATTCTT TAC CAT VPS41 Ensembl:ENSG00000006715 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs796520163 Functional Loss MNV dbSNP153 31..33 33 - - - 38605 RMVar_ID_38605 Human_SNP_ID_317413883 A-to-I Human chr7 - 38723460 38723460 38723460 TCGGCCTTCCGAAGTGTTAGGATTACAGGCGTAAGTCACCATGCCCAGCCAAGAAAGCTATTCTT TCGGCCTTCCGAAGTGTTAGGATTACAGGCGTTAGTCACCATGCCCAGCCAAGAAAGCTATTCTT T A VPS41 Ensembl:ENSG00000006715 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs3207255 Functional Loss SNV dbSNP153 33..33 33 - - - 38606 RMVar_ID_38606 Human_SNP_ID_317413884 A-to-I Human chr7 - 38723460 38723460 38723460 TCGGCCTTCCGAAGTGTTAGGATTACAGGCGTAAGTCACCATGCCCAGCCAAGAAAGCTATTCTT TCGGCCTTCCGAAGTGTTAGGATTACAGGCGTGAGTCACCATGCCCAGCCAAGAAAGCTATTCTT T C VPS41 Ensembl:ENSG00000006715 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs3207255 Functional Loss SNV dbSNP153 33..33 33 - - - 38607 RMVar_ID_38607 Human_SNP_ID_317413906 A-to-I Human chr7 - 38723544 38723544 38723544 AATTTTTTGTACTTTGGTAGAGATGAGGTTTCACCATGTTGCCCAAGCTGGTCTCGAACTCCTGA AATTTTTTGTACTTTGGTAGAGATGAGGTTTCGCCATGTTGCCCAAGCTGGTCTCGAACTCCTGA T C VPS41 Ensembl:ENSG00000006715 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs371695370 Functional Loss SNV dbSNP153 33..33 33 - - - 38608 RMVar_ID_38608 Human_SNP_ID_317414251 A-to-I Human chr7 - 38724659 38724659 38724659 ACCCCAGGAGACGTAGGTTGTGGTGAGCTGAGATCGCGCCATTGCACTCCAGCCTGGGCAACAAG ACCCCAGGAGACGTAGGTTGTGGTGAGCTGAGGTCGCGCCATTGCACTCCAGCCTGGGCAACAAG T C VPS41 Ensembl:ENSG00000006715 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1138237 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16149050 38609 RMVar_ID_38609 Human_SNP_ID_317414267 A-to-I Human chr7 - 38724686 38724686 38724686 AGGAGGCTGAGGCAGGAGAATCACTTGACCCCAGGAGACGTAGGTTGTGGTGAGCTGAGATCGCG AGGAGGCTGAGGCAGGAGAATCACTTGACCCCGGGAGACGTAGGTTGTGGTGAGCTGAGATCGCG T C VPS41 Ensembl:ENSG00000006715 Protein coding 3'UTR GSE100210;GSE107867;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,30559470,31158229,31158229 RNA-Seq:(High) rs1405625194 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_683896,Human_RBP_ID_16149050 38610 RMVar_ID_38610 Human_SNP_ID_317414275 A-to-I Human chr7 - 38724740 38724740 38724740 TAAAAACACAAATTAGCCAGGCGTGGTGGTACATGCCTGTAATCCCAGCTACTCAGGAGGCTGAG TAAAAACACAAATTAGCCAGGCGTGGTGGTACGTGCCTGTAATCCCAGCTACTCAGGAGGCTGAG T C VPS41 Ensembl:ENSG00000006715 Protein coding 3'UTR GSE47997;GSE38233;GSE38233;GSE112787 K562 cells&HepG2 cells;cultured B-cells;cultured B-cells;293 Flip-In T-REx cells,empty vector - 23474544,24183664,24183664,29967493 RNA-Seq:(High) rs560545292 Functional Loss SNV dbSNP153 33..33 33 - - - 38611 RMVar_ID_38611 Human_SNP_ID_317414286 A-to-I Human chr7 - 38724793 38724793 38724793 GAGATCGCACGTTCGAGACCAGCCTGACCAACATGGAGAAACCCCATCTCTACTAAAAACACAAA GAGATCGCACGTTCGAGACCAGCCTGACCAACGTGGAGAAACCCCATCTCTACTAAAAACACAAA T C VPS41 Ensembl:ENSG00000006715 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1137502 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_176330 38612 RMVar_ID_38612 Human_SNP_ID_317414305 A-to-I Human chr7 - 38724859 38724859 38724859 AGCCGGGCATGGTGGCTCACGCCCGTAATCCCAGGGCTTTGGGAGGCCTTGGCAGGTGGATCACC AGCCGGGCATGGTGGCTCACGCCCGTAATCCCGGGGCTTTGGGAGGCCTTGGCAGGTGGATCACC T C VPS41 Ensembl:ENSG00000006715 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1137501 Functional Loss SNV dbSNP153 33..33 33 - - - 38613 RMVar_ID_38613 Human_SNP_ID_317435307 A-to-I Human chr7 - 38817382 38817382 38817382 CCTGGCTGGTCTTGAACTCTTGACCTCAGGTGATCTGCTCTCCTCGGCCTCCCAAAGCCCTGGGA CCTGGCTGGTCTTGAACTCTTGACCTCAGGTGGTCTGCTCTCCTCGGCCTCCCAAAGCCCTGGGA T C VPS41 Ensembl:ENSG00000006715 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1436649834 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_363123,RMVar_hsa_circ_76428,RMVar_hsa_circ_93648,RMVar_hsa_circ_244711,RMVar_hsa_circ_108995,RMVar_hsa_circ_244712,RMVar_hsa_circ_244713,RMVar_hsa_circ_33332,RMVar_hsa_circ_360274,RMVar_hsa_circ_360191,RMVar_hsa_circ_244717 38614 RMVar_ID_38614 Human_SNP_ID_317611101 A-to-I Human chr7 + 39580452 39580452 39580452 TCTGCTCTTTCCAAAAAGAAGATCAAAGTACTAATCAGAACTACCTACAGATTGAGTTCTGCGGA TCTGCTCTTTCCAAAAAGAAGATCAAAGTACTGATCAGAACTACCTACAGATTGAGTTCTGCGGA A G YAE1 Ensembl:ENSG00000241127 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1018074948 Functional Loss SNV dbSNP153 33..33 33 - - - 38615 RMVar_ID_38615 Human_SNP_ID_317611377 A-to-I Human chr7 + 39581748 39581748 39581748 ACAAAATCAACCGGGCATGGTAGTGCACACCTATGGTCCCAACTACTTGGGAAGGCTGAGGCAGA ACAAAATCAACCGGGCATGGTAGTGCACACCTGTGGTCCCAACTACTTGGGAAGGCTGAGGCAGA A G YAE1 Ensembl:ENSG00000241127 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs555088021 Functional Loss SNV dbSNP153 33..33 33 - - - 38616 RMVar_ID_38616 Human_SNP_ID_317611429 A-to-I Human chr7 + 39581959 39581955 39581959 AAGTTAATTTTTTTTTTAAGAGATGGAGTCTCACTCTGTCACTAAGGTTGGAGTGCAGTGGTACA AAGTTAATTTTTTTTTTAAGAGATGGAGT____CTCTGTCACTAAGGTTGGAGTGCAGTGGTACA TCTCA T YAE1 Ensembl:ENSG00000241127 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs932441346 Functional Loss DEL dbSNP153 30..33 33 - - - 38617 RMVar_ID_38617 Human_SNP_ID_317611446 A-to-I Human chr7 + 39582057 39582047 39582058 TCAAGCAATCCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCACTACACCAGCTTCTGA TCAAGCAATCCTCCTGCCTCAGC___________CTGGGACTACAGGCACTACACCAGCTTCTGA CCTCCCAAGTAG C YAE1 Ensembl:ENSG00000241127 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1177493915 Functional Loss DEL dbSNP153 24..34 33 - - - 38618 RMVar_ID_38618 Human_SNP_ID_317611491 A-to-I Human chr7 + 39582267 39582267 39582267 GTTGCCTGGGCTAGTCTAGAACTCCTGGGCTCAAGTGATCCTCCTCCCTCGGCCTCCCAAAGTGC GTTGCCTGGGCTAGTCTAGAACTCCTGGGCTCCAGTGATCCTCCTCCCTCGGCCTCCCAAAGTGC A C YAE1 Ensembl:ENSG00000241127 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978518364 Functional Loss SNV dbSNP153 33..33 33 - - - 38619 RMVar_ID_38619 Human_SNP_ID_317660022 A-to-I Human chr7 + 39793397 39793397 39793397 AGGGACTTGGCCCCGGGAGGCCGCGGTGGGGCAAGAGCTTGGCCTGGAGACGCCCCTGGGAGGCA AGGGACTTGGCCCCGGGAGGCCGCGGTGGGGCGAGAGCTTGGCCTGGAGACGCCCCTGGGAGGCA A G LINC00265,LINC00265:2,LINC00265:3,LINC00265:4,LINC00265:5,LINC00265:6,LINC00265:7,LINC00265:8,LINC00265:9,LINC00265:10,LINC00265:11,LINC00265:12 RNACentral:URS0000D5DBF0,RNACentral:URS0000EB8ED8,RNACentral:URS0000D57390,RNACentral:URS00009BA799,RNACentral:URS0000D5D33E,RNACentral:URS0000D5DA46,RNACentral:URS0000D5CB77,RNACentral:URS00009BEE62,RNACentral:URS0000D5D3C2,RNACentral:URS00009B0E33,RNACentral:URS000075CC82,RNACentral:URS00008C0C82 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,intron,exon,exon,exon,intron,exon,exon,exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs549167269 Functional Loss SNV dbSNP153 33..33 33 - - - 38620 RMVar_ID_38620 Human_SNP_ID_317700567 A-to-I Human chr7 + 39960464 39960464 39960464 TGTTTTCAGTAGAGACGGGGTTTCATCATTTTACCCAGGATGGTCTTAATCTCCTGACCTCGTGA TGTTTTCAGTAGAGACGGGGTTTCATCATTTTGCCCAGGATGGTCTTAATCTCCTGACCTCGTGA A G CDK13 Ensembl:ENSG00000065883 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs984839535 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18100043 RMVar_hsa_circ_244747,RMVar_hsa_circ_115465,RMVar_hsa_circ_244746 38621 RMVar_ID_38621 Human_SNP_ID_317700571 A-to-I Human chr7 + 39960479 39960479 39960479 CGGGGTTTCATCATTTTACCCAGGATGGTCTTAATCTCCTGACCTCGTGATCCGCCCGCCTTGGC CGGGGTTTCATCATTTTACCCAGGATGGTCTTGATCTCCTGACCTCGTGATCCGCCCGCCTTGGC A G CDK13 Ensembl:ENSG00000065883 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947154892 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_244747,RMVar_hsa_circ_115465,RMVar_hsa_circ_244746 38622 RMVar_ID_38622 Human_SNP_ID_317700814 A-to-I Human chr7 + 39961238 39961238 39961238 AAACATAGCCAAGCATGGTGGCGTGTGCCTGTAGACCCCAACTACTCGGGAGACTGAGGCAGCAG AAACATAGCCAAGCATGGTGGCGTGTGCCTGTGGACCCCAACTACTCGGGAGACTGAGGCAGCAG A G CDK13 Ensembl:ENSG00000065883 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1369605600 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16151818 RMVar_hsa_circ_244747,RMVar_hsa_circ_115465,RMVar_hsa_circ_244746 38623 RMVar_ID_38623 Human_SNP_ID_317703413 A-to-I Human chr7 + 39970205 39970205 39970205 TTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTCCTGACCT TTTTGTATTTTTAGTAGAGACAGGGTTTCACCGTGTTGGCCAGGCTGGTCTCAAACTCCTGACCT A G CDK13 Ensembl:ENSG00000065883 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560294705 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_244747,RMVar_hsa_circ_115465,RMVar_hsa_circ_244746 38624 RMVar_ID_38624 Human_SNP_ID_317703826 A-to-I Human chr7 + 39971762 39971762 39971762 AAAATTAGCCGGACGTGGTGGCGGGCGCCTATAGTCCCAGCTACTTGGGAGGCTGAGGCAGAAGA AAAATTAGCCGGACGTGGTGGCGGGCGCCTATCGTCCCAGCTACTTGGGAGGCTGAGGCAGAAGA A C CDK13 Ensembl:ENSG00000065883 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1018023589 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_244747,RMVar_hsa_circ_115465,RMVar_hsa_circ_244746 38625 RMVar_ID_38625 Human_SNP_ID_317703827 A-to-I Human chr7 + 39971762 39971762 39971762 AAAATTAGCCGGACGTGGTGGCGGGCGCCTATAGTCCCAGCTACTTGGGAGGCTGAGGCAGAAGA AAAATTAGCCGGACGTGGTGGCGGGCGCCTATGGTCCCAGCTACTTGGGAGGCTGAGGCAGAAGA A G CDK13 Ensembl:ENSG00000065883 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1018023589 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_244747,RMVar_hsa_circ_115465,RMVar_hsa_circ_244746 38626 RMVar_ID_38626 Human_SNP_ID_317709519 A-to-I Human chr7 + 39991874 39991874 39991874 AGGAGTTTGAGAGGAGCCTCGGCAACATGGTGAAACCCCATCTCTTCAAAAAATACAAAAATTAG AGGAGTTTGAGAGGAGCCTCGGCAACATGGTGCAACCCCATCTCTTCAAAAAATACAAAAATTAG A C CDK13 Ensembl:ENSG00000065883 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202765909 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34843,RMVar_hsa_circ_244747,RMVar_hsa_circ_115465,RMVar_hsa_circ_244746,RMVar_hsa_circ_278233,RMVar_hsa_circ_316887,RMVar_hsa_circ_244748,RMVar_hsa_circ_244749,RMVar_hsa_circ_339569,RMVar_hsa_circ_342123,RMVar_hsa_circ_288388,RMVar_hsa_circ_305755,RMVar_hsa_circ_281489,RMVar_hsa_circ_273300,RMVar_hsa_circ_61522,RMVar_hsa_circ_244753,RMVar_hsa_circ_244755,RMVar_hsa_circ_244757,RMVar_hsa_circ_244758,RMVar_hsa_circ_244756,RMVar_hsa_circ_244754,RMVar_hsa_circ_244751,RMVar_hsa_circ_244752 38627 RMVar_ID_38627 Human_SNP_ID_317717346 A-to-I Human chr7 + 40020926 40020926 40020926 CATCCTGGCCAACATGGTGAAACACCATCTCTACCAAAAATACAAAAATTAGCAGGGCGTGGTAG CATCCTGGCCAACATGGTGAAACACCATCTCTGCCAAAAATACAAAAATTAGCAGGGCGTGGTAG A G CDK13 Ensembl:ENSG00000065883 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs962655154 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_244760,RMVar_hsa_circ_34843,RMVar_hsa_circ_244749,RMVar_hsa_circ_339569,RMVar_hsa_circ_342123,RMVar_hsa_circ_305755,RMVar_hsa_circ_281489,RMVar_hsa_circ_273300,RMVar_hsa_circ_61522,RMVar_hsa_circ_112048,RMVar_hsa_circ_244755,RMVar_hsa_circ_244757,RMVar_hsa_circ_244758,RMVar_hsa_circ_244756,RMVar_hsa_circ_244754,RMVar_hsa_circ_286249,RMVar_hsa_circ_336619,RMVar_hsa_circ_317563,RMVar_hsa_circ_59206,RMVar_hsa_circ_244761,RMVar_hsa_circ_69555,RMVar_hsa_circ_244764,RMVar_hsa_circ_299995,RMVar_hsa_circ_338752,RMVar_hsa_circ_244759,RMVar_hsa_circ_306771,RMVar_hsa_circ_244765,RMVar_hsa_circ_286674,RMVar_hsa_circ_244763,RMVar_hsa_circ_315806,RMVar_hsa_circ_285494,RMVar_hsa_circ_244766,RMVar_hsa_circ_244767 38628 RMVar_ID_38628 Human_SNP_ID_317727832 A-to-I Human chr7 + 40059429 40059429 40059429 TCACCCGGGCTGGAGTGCAGTGGCACGATGTCAGCTCACTGCAACCTCTGCCTCCAGGGTTTAAG TCACCCGGGCTGGAGTGCAGTGGCACGATGTCGGCTCACTGCAACCTCTGCCTCCAGGGTTTAAG A G CDK13 Ensembl:ENSG00000065883 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1426384266 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16153373 RMVar_hsa_circ_244760,RMVar_hsa_circ_34843,RMVar_hsa_circ_244749,RMVar_hsa_circ_339569,RMVar_hsa_circ_342123,RMVar_hsa_circ_305755,RMVar_hsa_circ_273300,RMVar_hsa_circ_112048,RMVar_hsa_circ_244755,RMVar_hsa_circ_244757,RMVar_hsa_circ_244758,RMVar_hsa_circ_244756,RMVar_hsa_circ_286249,RMVar_hsa_circ_336619,RMVar_hsa_circ_59206,RMVar_hsa_circ_8705,RMVar_hsa_circ_69555,RMVar_hsa_circ_244764,RMVar_hsa_circ_338752,RMVar_hsa_circ_244759,RMVar_hsa_circ_306771,RMVar_hsa_circ_244765,RMVar_hsa_circ_315806,RMVar_hsa_circ_285494,RMVar_hsa_circ_287526,RMVar_hsa_circ_244766,RMVar_hsa_circ_244767,RMVar_hsa_circ_293238,RMVar_hsa_circ_286112,RMVar_hsa_circ_244770,RMVar_hsa_circ_244771,RMVar_hsa_circ_244769,RMVar_hsa_circ_344605,RMVar_hsa_circ_244772 38629 RMVar_ID_38629 Human_SNP_ID_317728179 A-to-I Human chr7 + 40060872 40060872 40060872 CGCAGATCACCTGAGGTCAGGAATTTGAGACCAGCCTGGCCAACATGGCAAAACCCTGTCTCTAC CGCAGATCACCTGAGGTCAGGAATTTGAGACCGGCCTGGCCAACATGGCAAAACCCTGTCTCTAC A G CDK13 Ensembl:ENSG00000065883 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1019489245 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_244760,RMVar_hsa_circ_34843,RMVar_hsa_circ_244749,RMVar_hsa_circ_339569,RMVar_hsa_circ_342123,RMVar_hsa_circ_305755,RMVar_hsa_circ_273300,RMVar_hsa_circ_112048,RMVar_hsa_circ_244755,RMVar_hsa_circ_244757,RMVar_hsa_circ_244758,RMVar_hsa_circ_244756,RMVar_hsa_circ_286249,RMVar_hsa_circ_336619,RMVar_hsa_circ_59206,RMVar_hsa_circ_8705,RMVar_hsa_circ_69555,RMVar_hsa_circ_244764,RMVar_hsa_circ_338752,RMVar_hsa_circ_244759,RMVar_hsa_circ_306771,RMVar_hsa_circ_244765,RMVar_hsa_circ_315806,RMVar_hsa_circ_285494,RMVar_hsa_circ_287526,RMVar_hsa_circ_244766,RMVar_hsa_circ_244767,RMVar_hsa_circ_293238,RMVar_hsa_circ_286112,RMVar_hsa_circ_244770,RMVar_hsa_circ_244771,RMVar_hsa_circ_244769,RMVar_hsa_circ_344605,RMVar_hsa_circ_244772 38630 RMVar_ID_38630 Human_SNP_ID_317728911 A-to-I Human chr7 + 40063689 40063689 40063689 TTTATTATTTTATTTTTTTGAGATAGAGTCTCACTCTGTCACCTAGGCTGGAGTGCAGTGGCATG TTTATTATTTTATTTTTTTGAGATAGAGTCTCCCTCTGTCACCTAGGCTGGAGTGCAGTGGCATG A C CDK13 Ensembl:ENSG00000065883 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs910144130 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34843,RMVar_hsa_circ_342123,RMVar_hsa_circ_305755,RMVar_hsa_circ_112048,RMVar_hsa_circ_244758,RMVar_hsa_circ_336619,RMVar_hsa_circ_8705,RMVar_hsa_circ_69555,RMVar_hsa_circ_338752,RMVar_hsa_circ_244759,RMVar_hsa_circ_244765,RMVar_hsa_circ_315806,RMVar_hsa_circ_287526,RMVar_hsa_circ_244767,RMVar_hsa_circ_286112,RMVar_hsa_circ_244770,RMVar_hsa_circ_244771,RMVar_hsa_circ_296014,RMVar_hsa_circ_309634,RMVar_hsa_circ_349054,RMVar_hsa_circ_244775,RMVar_hsa_circ_244774 38631 RMVar_ID_38631 Human_SNP_ID_317729246 A-to-I Human chr7 + 40064823 40064809 40064824 TTTTTTTTTCCTGTTTTTTGAGACAGTATCTCACTTTGTTGCCTAGGCTGGAGTGCATTGGGGCA TTTTTTTTTCCTGTTTTTT_______________TTTGTTGCCTAGGCTGGAGTGCATTGGGGCA TGAGACAGTATCTCAC T CDK13 Ensembl:ENSG00000065883 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1429198675 Functional Loss DEL dbSNP153 20..34 33 - - - Human_RBP_ID_7738181 RMVar_hsa_circ_34843,RMVar_hsa_circ_342123,RMVar_hsa_circ_305755,RMVar_hsa_circ_112048,RMVar_hsa_circ_244758,RMVar_hsa_circ_336619,RMVar_hsa_circ_8705,RMVar_hsa_circ_69555,RMVar_hsa_circ_338752,RMVar_hsa_circ_244759,RMVar_hsa_circ_244765,RMVar_hsa_circ_315806,RMVar_hsa_circ_287526,RMVar_hsa_circ_244767,RMVar_hsa_circ_286112,RMVar_hsa_circ_244770,RMVar_hsa_circ_244771,RMVar_hsa_circ_296014,RMVar_hsa_circ_309634,RMVar_hsa_circ_349054,RMVar_hsa_circ_244775,RMVar_hsa_circ_244774 38632 RMVar_ID_38632 Human_SNP_ID_317729278 A-to-I Human chr7 + 40064917 40064917 40064917 GGAGCCAAACAATCCTCCTGCCTCAGCCTTCCAAGTAGCTGGGACCACAGGCATGCACCACCATG GGAGCCAAACAATCCTCCTGCCTCAGCCTTCCGAGTAGCTGGGACCACAGGCATGCACCACCATG A G CDK13 Ensembl:ENSG00000065883 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1013134512 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34843,RMVar_hsa_circ_342123,RMVar_hsa_circ_305755,RMVar_hsa_circ_112048,RMVar_hsa_circ_244758,RMVar_hsa_circ_336619,RMVar_hsa_circ_8705,RMVar_hsa_circ_69555,RMVar_hsa_circ_338752,RMVar_hsa_circ_244759,RMVar_hsa_circ_244765,RMVar_hsa_circ_315806,RMVar_hsa_circ_287526,RMVar_hsa_circ_244767,RMVar_hsa_circ_286112,RMVar_hsa_circ_244770,RMVar_hsa_circ_244771,RMVar_hsa_circ_296014,RMVar_hsa_circ_309634,RMVar_hsa_circ_349054,RMVar_hsa_circ_244775,RMVar_hsa_circ_244774 38633 RMVar_ID_38633 Human_SNP_ID_317729279 A-to-I Human chr7 + 40064917 40064917 40064917 GGAGCCAAACAATCCTCCTGCCTCAGCCTTCCAAGTAGCTGGGACCACAGGCATGCACCACCATG GGAGCCAAACAATCCTCCTGCCTCAGCCTTCCTAGTAGCTGGGACCACAGGCATGCACCACCATG A T CDK13 Ensembl:ENSG00000065883 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1013134512 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34843,RMVar_hsa_circ_342123,RMVar_hsa_circ_305755,RMVar_hsa_circ_112048,RMVar_hsa_circ_244758,RMVar_hsa_circ_336619,RMVar_hsa_circ_8705,RMVar_hsa_circ_69555,RMVar_hsa_circ_338752,RMVar_hsa_circ_244759,RMVar_hsa_circ_244765,RMVar_hsa_circ_315806,RMVar_hsa_circ_287526,RMVar_hsa_circ_244767,RMVar_hsa_circ_286112,RMVar_hsa_circ_244770,RMVar_hsa_circ_244771,RMVar_hsa_circ_296014,RMVar_hsa_circ_309634,RMVar_hsa_circ_349054,RMVar_hsa_circ_244775,RMVar_hsa_circ_244774 38634 RMVar_ID_38634 Human_SNP_ID_317730268 A-to-I Human chr7 + 40068573 40068572 40068573 AAAATTACCTGGGCGCAGTGGTGTGTGCCTGTAATCCCAGCTACTTGGAAGGCTGAGGCAGGAAC AAAATTACCTGGGCGCAGTGGTGTGTGCCTGT_ATCCCAGCTACTTGGAAGGCTGAGGCAGGAAC TA T CDK13 Ensembl:ENSG00000065883 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1198304261 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_18107989 RMVar_hsa_circ_34843,RMVar_hsa_circ_342123,RMVar_hsa_circ_305755,RMVar_hsa_circ_112048,RMVar_hsa_circ_244758,RMVar_hsa_circ_336619,RMVar_hsa_circ_8705,RMVar_hsa_circ_69555,RMVar_hsa_circ_338752,RMVar_hsa_circ_244759,RMVar_hsa_circ_244765,RMVar_hsa_circ_315806,RMVar_hsa_circ_287526,RMVar_hsa_circ_244767,RMVar_hsa_circ_286112,RMVar_hsa_circ_244770,RMVar_hsa_circ_244771,RMVar_hsa_circ_296014,RMVar_hsa_circ_309634,RMVar_hsa_circ_349054,RMVar_hsa_circ_244775,RMVar_hsa_circ_244774 38635 RMVar_ID_38635 Human_SNP_ID_317731594 A-to-I Human chr7 + 40073362 40073362 40073362 GGCTACATATTATTAAATTTTTGTTTGTGGCCAGGAATGATGACTGACACCTGTAATGCTAGCAC GGCTACATATTATTAAATTTTTGTTTGTGGCCGGGAATGATGACTGACACCTGTAATGCTAGCAC A G CDK13 Ensembl:ENSG00000065883 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs960702814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3088234,Human_RBP_ID_16153569 RMVar_hsa_circ_34843,RMVar_hsa_circ_342123,RMVar_hsa_circ_305755,RMVar_hsa_circ_244758,RMVar_hsa_circ_336619,RMVar_hsa_circ_8705,RMVar_hsa_circ_69555,RMVar_hsa_circ_338752,RMVar_hsa_circ_244765,RMVar_hsa_circ_315806,RMVar_hsa_circ_287526,RMVar_hsa_circ_244767,RMVar_hsa_circ_286112,RMVar_hsa_circ_244770,RMVar_hsa_circ_244771,RMVar_hsa_circ_296014,RMVar_hsa_circ_309634,RMVar_hsa_circ_349054,RMVar_hsa_circ_244775,RMVar_hsa_circ_244774 38636 RMVar_ID_38636 Human_SNP_ID_317731828 A-to-I Human chr7 + 40073919 40073919 40073919 GCCTTTCTTTTTTTCCTTTTTTTTTTTTTTTTAAGATAAAGTCTTGCTGTCTGTCATCCAGGCTG GCCTTTCTTTTTTTCCTTTTTTTTTTTTTTTTTAGATAAAGTCTTGCTGTCTGTCATCCAGGCTG A T CDK13 Ensembl:ENSG00000065883 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1488455664 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16153576 RMVar_hsa_circ_34843,RMVar_hsa_circ_342123,RMVar_hsa_circ_305755,RMVar_hsa_circ_244758,RMVar_hsa_circ_336619,RMVar_hsa_circ_8705,RMVar_hsa_circ_69555,RMVar_hsa_circ_338752,RMVar_hsa_circ_244765,RMVar_hsa_circ_315806,RMVar_hsa_circ_287526,RMVar_hsa_circ_244767,RMVar_hsa_circ_286112,RMVar_hsa_circ_244770,RMVar_hsa_circ_244771,RMVar_hsa_circ_296014,RMVar_hsa_circ_309634,RMVar_hsa_circ_349054,RMVar_hsa_circ_244775,RMVar_hsa_circ_244774 38637 RMVar_ID_38637 Human_SNP_ID_317731829 A-to-I Human chr7 + 40073925 40073923 40073925 CTTTTTTTCCTTTTTTTTTTTTTTTTAAGATAAAGTCTTGCTGTCTGTCATCCAGGCTGGAGTGC CTTTTTTTCCTTTTTTTTTTTTTTTTAAGAT__AGTCTTGCTGTCTGTCATCCAGGCTGGAGTGC TAA T CDK13 Ensembl:ENSG00000065883 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1290773750 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_16153576 RMVar_hsa_circ_34843,RMVar_hsa_circ_342123,RMVar_hsa_circ_305755,RMVar_hsa_circ_244758,RMVar_hsa_circ_336619,RMVar_hsa_circ_8705,RMVar_hsa_circ_69555,RMVar_hsa_circ_338752,RMVar_hsa_circ_244765,RMVar_hsa_circ_315806,RMVar_hsa_circ_287526,RMVar_hsa_circ_244767,RMVar_hsa_circ_286112,RMVar_hsa_circ_244770,RMVar_hsa_circ_244771,RMVar_hsa_circ_296014,RMVar_hsa_circ_309634,RMVar_hsa_circ_349054,RMVar_hsa_circ_244775,RMVar_hsa_circ_244774 38638 RMVar_ID_38638 Human_SNP_ID_317736098 A-to-I Human chr7 + 40090748 40090748 40090748 CTCTACAAAAAATACAAAAATTAGCCTGGCCTATATTCCCAGTTACTTGCGGGGCTGAAGCAGGA CTCTACAAAAAATACAAAAATTAGCCTGGCCTGTATTCCCAGTTACTTGCGGGGCTGAAGCAGGA A G CDK13 Ensembl:ENSG00000065883 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1018410237 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34843,RMVar_hsa_circ_86139,RMVar_hsa_circ_65352,RMVar_hsa_circ_244778,RMVar_hsa_circ_70280 38639 RMVar_ID_38639 Human_SNP_ID_317739127 A-to-I Human chr7 - 40102773 40102765 40102774 AAAATTAGCCGGGCATAGTGACATGTGCCTGTAAGTCCCGGCTGTTTGGGAGGCTGAGGCGGTAG AAAATTAGCCGGGCATAGTGACATGTGCCTG_________GCTGTTTGGGAGGCTGAGGCGGTAG CCGGGACTTA C RF00017-4569 RNACentral:URS000090668B SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1317381610 Functional Loss DEL dbSNP153 32..40 33 - - - 38640 RMVar_ID_38640 Human_SNP_ID_317739960 A-to-I Human chr7 - 40106307 40106307 40106307 TCCTTTCCAATTACTTCTTCTAATTTTTTTTTAGAAACAGGATCTCACTCTGTCACCCAGGCTGC TCCTTTCCAATTACTTCTTCTAATTTTTTTTTTGAAACAGGATCTCACTCTGTCACCCAGGCTGC T A RF00017-4569 RNACentral:URS000090668B SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1562774696 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16153657 38641 RMVar_ID_38641 Human_SNP_ID_318196492 A-to-I Human chr7 - 41964342 41964342 41964342 ACCTCCCTAGCGGAAGAAAGCAAATTCCTTGCAGTTATGCAATAGGCTTTAGGAAAAAAAGACTG ACCTCCCTAGCGGAAGAAAGCAAATTCCTTGCGGTTATGCAATAGGCTTTAGGAAAAAAAGACTG T C GLI3 Ensembl:ENSG00000106571 Protein coding CDS GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs750622081 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_354077 38642 RMVar_ID_38642 Human_SNP_ID_318400938 A-to-I Human chr7 + 42795579 42795579 42795579 GCACTCAACTGTGTGGTGGGATCCCAGGGCATACCCAAGAGAATTGTAAATGCAAAAATTGCTTG GCACTCAACTGTGTGGTGGGATCCCAGGGCATGCCCAAGAGAATTGTAAATGCAAAAATTGCTTG A G TCP1P1 Ensembl:ENSG00000229161 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs373694560 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7779111 38643 RMVar_ID_38643 Human_SNP_ID_318432058 A-to-I Human chr7 - 42925438 42925438 42925438 ATTAAACAGAGAAAAGAGGAGTTATGTACTCTATCTCCCTCCTCTTTCACATCTGAGTTATTCTC ATTAAACAGAGAAAAGAGGAGTTATGTACTCTGTCTCCCTCCTCTTTCACATCTGAGTTATTCTC T C PSMA2,AC010132.3 Ensembl:ENSG00000106588,Ensembl:ENSG00000256646 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs192905103 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5340,RMVar_hsa_circ_50200 38644 RMVar_ID_38644 Human_SNP_ID_318432059 A-to-I Human chr7 - 42925438 42925438 42925438 ATTAAACAGAGAAAAGAGGAGTTATGTACTCTATCTCCCTCCTCTTTCACATCTGAGTTATTCTC ATTAAACAGAGAAAAGAGGAGTTATGTACTCTCTCTCCCTCCTCTTTCACATCTGAGTTATTCTC T G PSMA2,AC010132.3 Ensembl:ENSG00000106588,Ensembl:ENSG00000256646 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs192905103 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5340,RMVar_hsa_circ_50200 38645 RMVar_ID_38645 Human_SNP_ID_318432075 A-to-I Human chr7 - 42925500 42925500 42925500 AACTAAAGCCTTATGCCCAGTTCCTGTATAGTAGAAGAGGAATATGTCAGAAAGGAAAGTCCATT AACTAAAGCCTTATGCCCAGTTCCTGTATAGTTGAAGAGGAATATGTCAGAAAGGAAAGTCCATT T A PSMA2,AC010132.3 Ensembl:ENSG00000106588,Ensembl:ENSG00000256646 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559802263 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5340,RMVar_hsa_circ_50200 38646 RMVar_ID_38646 Human_SNP_ID_318432085 A-to-I Human chr7 - 42925556 42925556 42925556 TAAGAGACAGGGTCATGCTGGGTATTGCTTTTATCATTTTAAACTGCACTGGAGAAAACTAAAGC TAAGAGACAGGGTCATGCTGGGTATTGCTTTTGTCATTTTAAACTGCACTGGAGAAAACTAAAGC T C PSMA2,AC010132.3 Ensembl:ENSG00000106588,Ensembl:ENSG00000256646 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1159027949 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5340,RMVar_hsa_circ_50200 38647 RMVar_ID_38647 Human_SNP_ID_318432189 A-to-I Human chr7 - 42926039 42926039 42926039 GTTGTTGAGTGTGGCAGCCAACCAGGATCCCAATGCTTGTGTAATCACCCCCTTTATATTTCACA GTTGTTGAGTGTGGCAGCCAACCAGGATCCCATTGCTTGTGTAATCACCCCCTTTATATTTCACA T A PSMA2,AC010132.3 Ensembl:ENSG00000106588,Ensembl:ENSG00000256646 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs653079 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_4351,GWAS_ID_4352,GWAS_ID_4353,GWAS_ID_4354,GWAS_ID_4355,GWAS_ID_4356,GWAS_ID_4357,GWAS_ID_4358,GWAS_ID_4359,GWAS_ID_4360,GWAS_ID_4361,GWAS_ID_4362,GWAS_ID_4363,GWAS_ID_4364,GWAS_ID_4365,GWAS_ID_4366,GWAS_ID_4367,GWAS_ID_4368,GWAS_ID_4369,GWAS_ID_4370,GWAS_ID_4371,GWAS_ID_4372,GWAS_ID_4373,GWAS_ID_4374,GWAS_ID_4375,GWAS_ID_4376,GWAS_ID_4377,GWAS_ID_4378,GWAS_ID_4379,GWAS_ID_4380,GWAS_ID_4381,GWAS_ID_4382,GWAS_ID_4383,GWAS_ID_4384 RMVar_hsa_circ_5340,RMVar_hsa_circ_50200 38648 RMVar_ID_38648 Human_SNP_ID_318432190 A-to-I Human chr7 - 42926039 42926039 42926039 GTTGTTGAGTGTGGCAGCCAACCAGGATCCCAATGCTTGTGTAATCACCCCCTTTATATTTCACA GTTGTTGAGTGTGGCAGCCAACCAGGATCCCAGTGCTTGTGTAATCACCCCCTTTATATTTCACA T C PSMA2,AC010132.3 Ensembl:ENSG00000106588,Ensembl:ENSG00000256646 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs653079 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_4351,GWAS_ID_4352,GWAS_ID_4353,GWAS_ID_4354,GWAS_ID_4355,GWAS_ID_4356,GWAS_ID_4357,GWAS_ID_4358,GWAS_ID_4359,GWAS_ID_4360,GWAS_ID_4361,GWAS_ID_4362,GWAS_ID_4363,GWAS_ID_4364,GWAS_ID_4365,GWAS_ID_4366,GWAS_ID_4367,GWAS_ID_4368,GWAS_ID_4369,GWAS_ID_4370,GWAS_ID_4371,GWAS_ID_4372,GWAS_ID_4373,GWAS_ID_4374,GWAS_ID_4375,GWAS_ID_4376,GWAS_ID_4377,GWAS_ID_4378,GWAS_ID_4379,GWAS_ID_4380,GWAS_ID_4381,GWAS_ID_4382,GWAS_ID_4383,GWAS_ID_4384 RMVar_hsa_circ_5340,RMVar_hsa_circ_50200 38649 RMVar_ID_38649 Human_SNP_ID_318432252 A-to-I Human chr7 - 42926290 42926290 42926290 GATAGATTACATAACTCCTCTTTTCTCTGTTCAGCGGACTTTCTCTTCTGACATATTCCTCTTCT GATAGATTACATAACTCCTCTTTTCTCTGTTCGGCGGACTTTCTCTTCTGACATATTCCTCTTCT T C PSMA2,AC010132.3 Ensembl:ENSG00000106588,Ensembl:ENSG00000256646 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs542275110 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5340,RMVar_hsa_circ_50200 38650 RMVar_ID_38650 Human_SNP_ID_318432264 A-to-I Human chr7 - 42926353 42926353 42926353 TGAATTTAGTTTGCCTGTATAGGTTACTTTAAAGAGAATAACTCAGATGTGAAAGAGGAGGTAGA TGAATTTAGTTTGCCTGTATAGGTTACTTTAAGGAGAATAACTCAGATGTGAAAGAGGAGGTAGA T C PSMA2,AC010132.3 Ensembl:ENSG00000106588,Ensembl:ENSG00000256646 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1375611889 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5340,RMVar_hsa_circ_50200 38651 RMVar_ID_38651 Human_SNP_ID_318586841 A-to-I Human chr7 + 43597511 43597511 43597511 TCAAGCGATTCTCCTGCCTCAGCCCCCCAAGTAGCTAGGATTACAGGCATCCGTCCACCTTTATG TCAAGCGATTCTCCTGCCTCAGCCCCCCAAGTGGCTAGGATTACAGGCATCCGTCCACCTTTATG A G STK17A Ensembl:ENSG00000164543 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1383353245 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_322078,RMVar_hsa_circ_282376,RMVar_hsa_circ_244849 38652 RMVar_ID_38652 Human_SNP_ID_318586843 A-to-I Human chr7 + 43597515 43597515 43597515 GCGATTCTCCTGCCTCAGCCCCCCAAGTAGCTAGGATTACAGGCATCCGTCCACCTTTATGCCTG GCGATTCTCCTGCCTCAGCCCCCCAAGTAGCTGGGATTACAGGCATCCGTCCACCTTTATGCCTG A G STK17A Ensembl:ENSG00000164543 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1182946569 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_322078,RMVar_hsa_circ_282376,RMVar_hsa_circ_244849 38653 RMVar_ID_38653 Human_SNP_ID_318587059 A-to-I Human chr7 + 43598349 43598349 43598349 AAAATTAGCTGGACATGGTAGCAGGCGCCTATAGTCCCAGCTACTCAGGAGGCTGACGCAGGAGA AAAATTAGCTGGACATGGTAGCAGGCGCCTATGGTCCCAGCTACTCAGGAGGCTGACGCAGGAGA A G STK17A Ensembl:ENSG00000164543 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1181974488 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_322078,RMVar_hsa_circ_282376,RMVar_hsa_circ_244849 38654 RMVar_ID_38654 Human_SNP_ID_318590515 A-to-I Human chr7 - 43613660 43613660 43613660 TTTTTAATTTTTTGTGGAGATGAGGTCTCACTATGTTGCCTGGGCTGGTCTCAAACTCCTGGGCT TTTTTAATTTTTTGTGGAGATGAGGTCTCACTGTGTTGCCTGGGCTGGTCTCAAACTCCTGGGCT T C COA1 Ensembl:ENSG00000106603 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1336356420 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16155573 RMVar_hsa_circ_102319,RMVar_hsa_circ_244851 38655 RMVar_ID_38655 Human_SNP_ID_318590948 A-to-I Human chr7 - 43615458 43615458 43615458 TAGTACAACAAAAGGGCTGGGCGCAGTGGCTCACATCTGTAATTCCAGCAATTTGGGAGGCCGAG TAGTACAACAAAAGGGCTGGGCGCAGTGGCTCCCATCTGTAATTCCAGCAATTTGGGAGGCCGAG T G COA1 Ensembl:ENSG00000106603 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs908165238 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102319,RMVar_hsa_circ_244851 38656 RMVar_ID_38656 Human_SNP_ID_318592355 A-to-I Human chr7 - 43621596 43621596 43621596 CGCTGTGCTGGCACGTGCCTGTGGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGGAGCTCAAGTT CGCTGTGCTGGCACGTGCCTGTGGTCCCAGCTGCTCGGGAGGCTGAGGCAGGAGGAGCTCAAGTT T C COA1 Ensembl:ENSG00000106603 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1458109735 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102319,RMVar_hsa_circ_244851 38657 RMVar_ID_38657 Human_SNP_ID_318593275 A-to-I Human chr7 - 43625102 43625101 43625103 TCTTTGTACACAAATTCTCATTCTGGAGAAACAGGATGTAGAATTCAAAGGTGCCAACATCTCCC TCTTTGTACACAAATTCTCATTCTGGAGAAA__GGATGTAGAATTCAAAGGTGCCAACATCTCCC CTG C COA1 Ensembl:ENSG00000106603 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1200604825 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_3089046,Human_RBP_ID_16155737 RMVar_hsa_circ_102319,RMVar_hsa_circ_244851 38658 RMVar_ID_38658 Human_SNP_ID_318595034 A-to-I Human chr7 - 43632411 43632407 43632411 CAAAATATCAACATTAATTGGAATTTGGAAGAAATAGATTCCAATCCTCATGGAGGACTTGGAGG CAAAATATCAACATTAATTGGAATTTGGAAGA____GATTCCAATCCTCATGGAGGACTTGGAGG CTATT C COA1 Ensembl:ENSG00000106603 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1389989334 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_3089132,Human_RBP_ID_22529303,Human_RBP_ID_23120489 38659 RMVar_ID_38659 Human_SNP_ID_318599751 A-to-I Human chr7 + 43649761 43649761 43649761 AAAGATTTGTATCTTTATTAAGACAGTTTGCCAACAGTTGGAAGTACTATAAAGTATCTTGAAGA AAAGATTTGTATCTTTATTAAGACAGTTTGCCGACAGTTGGAAGTACTATAAAGTATCTTGAAGA A G STK17A Ensembl:ENSG00000164543 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs561736151 Functional Loss SNV dbSNP153 33..33 33 - - - 38660 RMVar_ID_38660 Human_SNP_ID_318602405 A-to-I Human chr7 - 43661446 43661446 43661446 TATTTTTAGTAGAGACGGGGTTTCACTGTGTTAGCCAGAATGGTTTAGATTTCCTGACCTGTGAT TATTTTTAGTAGAGACGGGGTTTCACTGTGTTTGCCAGAATGGTTTAGATTTCCTGACCTGTGAT T A COA1 Ensembl:ENSG00000106603 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1466048051 Functional Loss SNV dbSNP153 33..33 33 - - - 38661 RMVar_ID_38661 Human_SNP_ID_318615201 A-to-I Human chr7 - 43713821 43713821 43713821 TTGGTCAGGCTGGTCTCGAACTCCTGATGTCAAATGATCTGCCCACCTTGGCCTCCCAAAGTGCT TTGGTCAGGCTGGTCTCGAACTCCTGATGTCAGATGATCTGCCCACCTTGGCCTCCCAAAGTGCT T C COA1 Ensembl:ENSG00000106603 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1224451185 Functional Loss SNV dbSNP153 33..33 33 - - - 38662 RMVar_ID_38662 Human_SNP_ID_318617222 A-to-I Human chr7 - 43722288 43722288 43722288 GAGTTTGAGACCAGCTTGGGCAAAGTGGCGAAACCCCATCTCTCTACTAAAAATACAAAAGAACT GAGTTTGAGACCAGCTTGGGCAAAGTGGCGAAGCCCCATCTCTCTACTAAAAATACAAAAGAACT T C COA1 Ensembl:ENSG00000106603 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs371274321 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1246649,Human_RBP_ID_16158319,Human_RBP_ID_18100518 38663 RMVar_ID_38663 Human_SNP_ID_318626793 A-to-I Human chr7 + 43762966 43762966 43762966 TACTGACATTTCTGATTGTCGTGCTGGGGGGAAAACGGTATGTGCCACTGGCATCTAGTGGGGAA TACTGACATTTCTGATTGTCGTGCTGGGGGGAGAACGGTATGTGCCACTGGCATCTAGTGGGGAA A G BLVRA Ensembl:ENSG00000106605 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1249882803 Functional Loss SNV dbSNP153 33..33 33 - - - 38664 RMVar_ID_38664 Human_SNP_ID_318627299 A-to-I Human chr7 + 43765449 43765449 43765449 AATTTTTGTAATTTTAGTAGAGACACGGTTTCACCATGTTGGCCAGGCTCGTCTTGAACTCCTGG AATTTTTGTAATTTTAGTAGAGACACGGTTTCGCCATGTTGGCCAGGCTCGTCTTGAACTCCTGG A G BLVRA Ensembl:ENSG00000106605 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs987746225 Functional Loss SNV dbSNP153 33..33 33 - - - 38665 RMVar_ID_38665 Human_SNP_ID_318657521 A-to-I Human chr7 - 43894962 43894962 43894962 GCAGTGGTGTGATCACAGCTTACTCAGCTTCAACCTCCCGGCCTCAAGCAATTTCCCCACCTCAG GCAGTGGTGTGATCACAGCTTACTCAGCTTCAGCCTCCCGGCCTCAAGCAATTTCCCCACCTCAG T C URGCP-MRPS24,URGCP Ensembl:ENSG00000270617,Ensembl:ENSG00000106608 Protein coding,Protein coding intron,intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1228340092 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_244869,RMVar_hsa_circ_95866 38666 RMVar_ID_38666 Human_SNP_ID_318657631 A-to-I Human chr7 - 43895457 43895453 43895457 TGGCAAGGCTGGTCTTGAACTCCTGGACTCAAACAATCCATCCACCTTGGCCTCCAGAAGTACTG TGGCAAGGCTGGTCTTGAACTCCTGGACTCAA____TCCATCCACCTTGGCCTCCAGAAGTACTG ATTGT A URGCP-MRPS24,URGCP Ensembl:ENSG00000270617,Ensembl:ENSG00000106608 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs768233783 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_16158808 RMVar_hsa_circ_244869,RMVar_hsa_circ_95866 38667 RMVar_ID_38667 Human_SNP_ID_318661307 A-to-I Human chr7 - 43910773 43910773 43910773 TGGCTCACTGTGGCTTCAGCCTCCCAGGCTCAAGAGATCCTACCATCTCAGCCTCCTGAGTAGCT TGGCTCACTGTGGCTTCAGCCTCCCAGGCTCAGGAGATCCTACCATCTCAGCCTCCTGAGTAGCT T C URGCP Ensembl:ENSG00000106608 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs554710024 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_860816,Human_Splice_Rec_860817 38668 RMVar_ID_38668 Human_SNP_ID_318661920 A-to-I Human chr7 - 43913493 43913493 43913493 ACTGTCAGGGCCAGGTGCGGTGGTTCACGCCTATAATCCCAGCACTTTGGGAGGCCGAGGCAGGC ACTGTCAGGGCCAGGTGCGGTGGTTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGC T C URGCP Ensembl:ENSG00000106608 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs774956573 Functional Loss SNV dbSNP153 33..33 33 - - - 38669 RMVar_ID_38669 Human_SNP_ID_318662878 A-to-I Human chr7 - 43917807 43917807 43917807 TGCCACCATGCCCAGCCAATTTTTTATTTTTTATAGAGACAGGGTCTCACTATGTTGCTGGAATA TGCCACCATGCCCAGCCAATTTTTTATTTTTTGTAGAGACAGGGTCTCACTATGTTGCTGGAATA T C URGCP Ensembl:ENSG00000106608 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1209419867 Functional Loss SNV dbSNP153 33..33 33 - - - 38670 RMVar_ID_38670 Human_SNP_ID_318663124 A-to-I Human chr7 - 43918776 43918776 43918776 TCCATGGTGCCCTTGGGGCTGATACCATGCTCAGTGCACAGCTGTTTCCAGAACTCGAACCCAAT TCCATGGTGCCCTTGGGGCTGATACCATGCTCGGTGCACAGCTGTTTCCAGAACTCGAACCCAAT T C URGCP Ensembl:ENSG00000106608 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1305111626 Functional Loss SNV dbSNP153 33..33 33 - - - 38671 RMVar_ID_38671 Human_SNP_ID_318663198 A-to-I Human chr7 + 43919066 43919066 43919066 GATCCATGAGGACATTTTTAACATCACAGACCAGGAGGCAGATGGTAGTGACAATCTAGATGGCT GATCCATGAGGACATTTTTAACATCACAGACCGGGAGGCAGATGGTAGTGACAATCTAGATGGCT A G TUBG1P Ensembl:ENSG00000237972 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1422975733 Functional Loss SNV dbSNP153 33..33 33 - - - 38672 RMVar_ID_38672 Human_SNP_ID_318663246 A-to-I Human chr7 - 43919282 43919282 43919282 TGTGCAGCACCACCACACAGTCTGCGTTCTGCATCAGCCTCTTGAGTGTGAGGAGTGAATTATAA TGTGCAGCACCACCACACAGTCTGCGTTCTGCCTCAGCCTCTTGAGTGTGAGGAGTGAATTATAA T G URGCP Ensembl:ENSG00000106608 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1385507793 Functional Loss SNV dbSNP153 33..33 33 - - - 38673 RMVar_ID_38673 Human_SNP_ID_318665569 A-to-I Human chr7 + 43929035 43929035 43929035 CAAGGACAGGCTGGGTACAGTGGCTCATGCCTATATCCCAGCACTCTGGGAGGCCGAGGCAGGTG CAAGGACAGGCTGGGTACAGTGGCTCATGCCTGTATCCCAGCACTCTGGGAGGCCGAGGCAGGTG A G UBE2D4 Ensembl:ENSG00000078967 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388007187 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77663,RMVar_hsa_circ_244871 38674 RMVar_ID_38674 Human_SNP_ID_318666784 A-to-I Human chr7 + 43933669 43933669 43933669 TGGAGGGTGAGACACCAGAATTGCTTGAACCCAGTAGGCAGAGGTTGCAGTGAGCCGAGATGGTG TGGAGGGTGAGACACCAGAATTGCTTGAACCCGGTAGGCAGAGGTTGCAGTGAGCCGAGATGGTG A G UBE2D4 Ensembl:ENSG00000078967 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1030206996 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77663,RMVar_hsa_circ_244871 38675 RMVar_ID_38675 Human_SNP_ID_318666788 A-to-I Human chr7 + 43933676 43933675 43933676 TGAGACACCAGAATTGCTTGAACCCAGTAGGCAGAGGTTGCAGTGAGCCGAGATGGTGCCAGTGT TGAGACACCAGAATTGCTTGAACCCAGTAGGC_GAGGTTGCAGTGAGCCGAGATGGTGCCAGTGT CA C UBE2D4 Ensembl:ENSG00000078967 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1380347574 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_77663,RMVar_hsa_circ_244871 38676 RMVar_ID_38676 Human_SNP_ID_318669064 A-to-I Human chr7 - 43944337 43944337 43944337 AATGCACAACCTGGCCAAGCGTGGTGGCTCACACTTGGAATCCCAGCACTTTGGGAGGCGGAGGT AATGCACAACCTGGCCAAGCGTGGTGGCTCACTCTTGGAATCCCAGCACTTTGGGAGGCGGAGGT T A POLR2J4 Ensembl:ENSG00000214783 lincRNA exon GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1273740846 Functional Loss SNV dbSNP153 33..33 33 - - - 38677 RMVar_ID_38677 Human_SNP_ID_318673637 A-to-I Human chr7 - 43964148 43964148 43964148 TGCACCTGTACCACCAGTGCAGTGGTGATCATAGCTCACTGTAGACTCCACCTCCTGGGTGCAAG TGCACCTGTACCACCAGTGCAGTGGTGATCATGGCTCACTGTAGACTCCACCTCCTGGGTGCAAG T C POLR2J4,AC004951.3,AC004951.4 Ensembl:ENSG00000214783,Ensembl:ENSG00000241057,Ensembl:ENSG00000273432 lincRNA,Pseudogene,lincRNA intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1240206203 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5251126,Human_RBP_ID_8272098,Human_RBP_ID_16159078 RMVar_hsa_circ_89291,RMVar_hsa_circ_93469,RMVar_hsa_circ_244875,RMVar_hsa_circ_119287,RMVar_hsa_circ_244876,RMVar_hsa_circ_244878,RMVar_hsa_circ_98844,RMVar_hsa_circ_244877,RMVar_hsa_circ_117199,RMVar_hsa_circ_244880 38678 RMVar_ID_38678 Human_SNP_ID_318675311 A-to-I Human chr7 - 43970211 43970211 43970211 TGGAGTGCAATGGTGCGATCTGAGTTCAAGTAATTCTCCTGCCTCAGCCTCCTGAGGAGCTGGGA TGGAGTGCAATGGTGCGATCTGAGTTCAAGTACTTCTCCTGCCTCAGCCTCCTGAGGAGCTGGGA T G POLR2J4,AC004951.3,AC004951.4 Ensembl:ENSG00000214783,Ensembl:ENSG00000241057,Ensembl:ENSG00000273432 lincRNA,Pseudogene,lincRNA intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1218388161 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89291,RMVar_hsa_circ_93469,RMVar_hsa_circ_244875,RMVar_hsa_circ_119287,RMVar_hsa_circ_244876,RMVar_hsa_circ_244878,RMVar_hsa_circ_98844,RMVar_hsa_circ_244877,RMVar_hsa_circ_117199,RMVar_hsa_circ_308266,RMVar_hsa_circ_244880,RMVar_hsa_circ_277791,RMVar_hsa_circ_244881,RMVar_hsa_circ_31787 38679 RMVar_ID_38679 Human_SNP_ID_318675452 A-to-I Human chr7 - 43970647 43970647 43970647 GGCTGGGTACAGCGGCCCACACTTATAATCCCAGCACCTTAGGAGGCTGAGGTGGGAGGATGGCT GGCTGGGTACAGCGGCCCACACTTATAATCCCGGCACCTTAGGAGGCTGAGGTGGGAGGATGGCT T C POLR2J4,AC004951.3,AC004951.4 Ensembl:ENSG00000214783,Ensembl:ENSG00000241057,Ensembl:ENSG00000273432 lincRNA,Pseudogene,lincRNA intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1380711610 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89291,RMVar_hsa_circ_93469,RMVar_hsa_circ_244875,RMVar_hsa_circ_119287,RMVar_hsa_circ_244876,RMVar_hsa_circ_244878,RMVar_hsa_circ_98844,RMVar_hsa_circ_244877,RMVar_hsa_circ_117199,RMVar_hsa_circ_308266,RMVar_hsa_circ_244880,RMVar_hsa_circ_277791,RMVar_hsa_circ_244881,RMVar_hsa_circ_31787 38680 RMVar_ID_38680 Human_SNP_ID_318675454 A-to-I Human chr7 - 43970652 43970652 43970652 AATCTGGCTGGGTACAGCGGCCCACACTTATAATCCCAGCACCTTAGGAGGCTGAGGTGGGAGGA AATCTGGCTGGGTACAGCGGCCCACACTTATACTCCCAGCACCTTAGGAGGCTGAGGTGGGAGGA T G POLR2J4,AC004951.3,AC004951.4 Ensembl:ENSG00000214783,Ensembl:ENSG00000241057,Ensembl:ENSG00000273432 lincRNA,Pseudogene,lincRNA intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1338885949 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89291,RMVar_hsa_circ_93469,RMVar_hsa_circ_244875,RMVar_hsa_circ_119287,RMVar_hsa_circ_244876,RMVar_hsa_circ_244878,RMVar_hsa_circ_98844,RMVar_hsa_circ_244877,RMVar_hsa_circ_117199,RMVar_hsa_circ_308266,RMVar_hsa_circ_244880,RMVar_hsa_circ_277791,RMVar_hsa_circ_244881,RMVar_hsa_circ_31787 38681 RMVar_ID_38681 Human_SNP_ID_318677312 A-to-I Human chr7 - 43977825 43977821 43977825 GGGAGAAAGAAAGGGAGAGAGAGAGAGAGAGAAAGATGAAAGAAAGAAAAAGAAAGCAAAGAAAG GGGAGAAAGAAAGGGAGAGAGAGAGAGAGAGA____TGAAAGAAAGAAAAAGAAAGCAAAGAAAG ATCTT A POLR2J4,AC004951.4 Ensembl:ENSG00000214783,Ensembl:ENSG00000273432 lincRNA,lincRNA intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs767840783 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_26137960 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 38682 RMVar_ID_38682 Human_SNP_ID_318677315 A-to-I Human chr7 - 43977825 43977823 43977825 GGGAGAAAGAAAGGGAGAGAGAGAGAGAGAGAAAGATGAAAGAAAGAAAAAGAAAGCAAAGAAAG GGGAGAAAGAAAGGGAGAGAGAGAGAGAGAGA__GATGAAAGAAAGAAAAAGAAAGCAAAGAAAG CTT C POLR2J4,AC004951.4 Ensembl:ENSG00000214783,Ensembl:ENSG00000273432 lincRNA,lincRNA intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1554299137 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_26137960 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 38683 RMVar_ID_38683 Human_SNP_ID_318677317 A-to-I Human chr7 - 43977825 43977825 43977825 GGGAGAAAGAAAGGGAGAGAGAGAGAGAGAGAAAGATGAAAGAAAGAAAAAGAAAGCAAAGAAAG GGGAGAAAGAAAGGGAGAGAGAGAGAGAGAGAGAGATGAAAGAAAGAAAAAGAAAGCAAAGAAAG T C POLR2J4,AC004951.4 Ensembl:ENSG00000214783,Ensembl:ENSG00000273432 lincRNA,lincRNA intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs560739134 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26137960 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 38684 RMVar_ID_38684 Human_SNP_ID_318678189 A-to-I Human chr7 - 43981303 43981303 43981303 GGTAGAGGCAGGGTCTCCGTCACCCAGGCTTGAGTGCAGTGGCACGATCATAGCTCACTGCAGCC GGTAGAGGCAGGGTCTCCGTCACCCAGGCTTGCGTGCAGTGGCACGATCATAGCTCACTGCAGCC T G POLR2J4,AC004951.4 Ensembl:ENSG00000214783,Ensembl:ENSG00000273432 lincRNA,lincRNA intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs79785929 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3867854,Human_RBP_ID_5251236 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 38685 RMVar_ID_38685 Human_SNP_ID_318678739 A-to-I Human chr7 - 43983536 43983536 43983536 TCAGCCTCCTGAGTAGCTTGGACTGTAGGTACATGGCACCATGTCTGGCTAATTTTTTAAATTTC TCAGCCTCCTGAGTAGCTTGGACTGTAGGTACGTGGCACCATGTCTGGCTAATTTTTTAAATTTC T C POLR2J4,AC004951.4 Ensembl:ENSG00000214783,Ensembl:ENSG00000273432 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917986726 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16159122 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 38686 RMVar_ID_38686 Human_SNP_ID_318678740 A-to-I Human chr7 - 43983538 43983538 43983538 CCTCAGCCTCCTGAGTAGCTTGGACTGTAGGTACATGGCACCATGTCTGGCTAATTTTTTAAATT CCTCAGCCTCCTGAGTAGCTTGGACTGTAGGTGCATGGCACCATGTCTGGCTAATTTTTTAAATT T C POLR2J4,AC004951.4 Ensembl:ENSG00000214783,Ensembl:ENSG00000273432 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs567238110 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16159122 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 38687 RMVar_ID_38687 Human_SNP_ID_318678763 A-to-I Human chr7 - 43983654 43983654 43983654 AATTTTTAATTTTTTTGTAGACATGGAATCTTACTCTGTTGCCCAGGCTGGAAAGAACAGTGGTG AATTTTTAATTTTTTTGTAGACATGGAATCTTCCTCTGTTGCCCAGGCTGGAAAGAACAGTGGTG T G POLR2J4,AC004951.4 Ensembl:ENSG00000214783,Ensembl:ENSG00000273432 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs931333534 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7740489,Human_RBP_ID_16159127 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 38688 RMVar_ID_38688 Human_SNP_ID_318678765 A-to-I Human chr7 - 43983659 43983659 43983659 TGGCTAATTTTTAATTTTTTTGTAGACATGGAATCTTACTCTGTTGCCCAGGCTGGAAAGAACAG TGGCTAATTTTTAATTTTTTTGTAGACATGGACTCTTACTCTGTTGCCCAGGCTGGAAAGAACAG T G POLR2J4,AC004951.4 Ensembl:ENSG00000214783,Ensembl:ENSG00000273432 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1240820636 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7740489,Human_RBP_ID_16159128 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 38689 RMVar_ID_38689 Human_SNP_ID_318678783 A-to-I Human chr7 - 43983712 43983712 43983712 CCCACCTCAGCCTCCTGAGAGTAGCTGGGACTACAGGCACATGACACCACGTCTGGCTAATTTTT CCCACCTCAGCCTCCTGAGAGTAGCTGGGACTCCAGGCACATGACACCACGTCTGGCTAATTTTT T G POLR2J4,AC004951.4 Ensembl:ENSG00000214783,Ensembl:ENSG00000273432 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1020038952 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 38690 RMVar_ID_38690 Human_SNP_ID_318681564 A-to-I Human chr7 - 43993411 43993411 43993411 GAAACCCTGTCTCTACTAAAAATACAAAAGTTAGCCAGGCGTGGTGGCATGTGCCCGTAATCTCA GAAACCCTGTCTCTACTAAAAATACAAAAGTTGGCCAGGCGTGGTGGCATGTGCCCGTAATCTCA T C POLR2J4,AC004951.4 Ensembl:ENSG00000214783,Ensembl:ENSG00000273432 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs758495280 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_31787,RMVar_hsa_circ_107215,RMVar_hsa_circ_116772,RMVar_hsa_circ_244883,RMVar_hsa_circ_244888,RMVar_hsa_circ_77569,RMVar_hsa_circ_101844,RMVar_hsa_circ_244889,RMVar_hsa_circ_244891 38691 RMVar_ID_38691 Human_SNP_ID_318683529 A-to-I Human chr7 - 44000231 44000231 44000231 ATTGGCCAGGCTGGCCTTGAACTCCTGACCTCAGATGATCCGCCCGCCTCGGCCTCCCAAAGTGC ATTGGCCAGGCTGGCCTTGAACTCCTGACCTCGGATGATCCGCCCGCCTCGGCCTCCCAAAGTGC T C POLR2J4,AC004951.4 Ensembl:ENSG00000214783,Ensembl:ENSG00000273432 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs543006000 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_31787,RMVar_hsa_circ_107215,RMVar_hsa_circ_116772,RMVar_hsa_circ_244883,RMVar_hsa_circ_244888,RMVar_hsa_circ_77569,RMVar_hsa_circ_101844,RMVar_hsa_circ_244889,RMVar_hsa_circ_244891 38692 RMVar_ID_38692 Human_SNP_ID_318683538 A-to-I Human chr7 - 44000256 44000256 44000256 TTTAGTAGAGATGGGGTTTCACCATATTGGCCAGGCTGGCCTTGAACTCCTGACCTCAGATGATC TTTAGTAGAGATGGGGTTTCACCATATTGGCCGGGCTGGCCTTGAACTCCTGACCTCAGATGATC T C POLR2J4,AC004951.4 Ensembl:ENSG00000214783,Ensembl:ENSG00000273432 lincRNA,lincRNA intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1402182154 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_31787,RMVar_hsa_circ_107215,RMVar_hsa_circ_116772,RMVar_hsa_circ_244883,RMVar_hsa_circ_244888,RMVar_hsa_circ_77569,RMVar_hsa_circ_101844,RMVar_hsa_circ_244889,RMVar_hsa_circ_244891 38693 RMVar_ID_38693 Human_SNP_ID_318683541 A-to-I Human chr7 - 44000263 44000263 44000263 TTATACTTTTAGTAGAGATGGGGTTTCACCATATTGGCCAGGCTGGCCTTGAACTCCTGACCTCA TTATACTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGCCTTGAACTCCTGACCTCA T C POLR2J4,AC004951.4 Ensembl:ENSG00000214783,Ensembl:ENSG00000273432 lincRNA,lincRNA intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1446549287 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_31787,RMVar_hsa_circ_107215,RMVar_hsa_circ_116772,RMVar_hsa_circ_244883,RMVar_hsa_circ_244888,RMVar_hsa_circ_77569,RMVar_hsa_circ_101844,RMVar_hsa_circ_244889,RMVar_hsa_circ_244891 38694 RMVar_ID_38694 Human_SNP_ID_318683551 A-to-I Human chr7 - 44000282 44000282 44000282 ACTACCACTTGGCTAATTTTTATACTTTTAGTAGAGATGGGGTTTCACCATATTGGCCAGGCTGG ACTACCACTTGGCTAATTTTTATACTTTTAGTGGAGATGGGGTTTCACCATATTGGCCAGGCTGG T C POLR2J4,AC004951.4 Ensembl:ENSG00000214783,Ensembl:ENSG00000273432 lincRNA,lincRNA intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1187136877 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_31787,RMVar_hsa_circ_107215,RMVar_hsa_circ_116772,RMVar_hsa_circ_244883,RMVar_hsa_circ_244888,RMVar_hsa_circ_77569,RMVar_hsa_circ_101844,RMVar_hsa_circ_244889,RMVar_hsa_circ_244891 38695 RMVar_ID_38695 Human_SNP_ID_318685369 A-to-I Human chr7 - 44006739 44006739 44006739 TGCGATGGCACACCTGTTAGGCCTAGCTACTCAGGAGGCTGAAGCATAAGAATTGTGTGAACCCA TGCGATGGCACACCTGTTAGGCCTAGCTACTCGGGAGGCTGAAGCATAAGAATTGTGTGAACCCA T C POLR2J4,AC004951.1,AC004951.4 Ensembl:ENSG00000214783,Ensembl:ENSG00000228434,Ensembl:ENSG00000273432 lincRNA,lincRNA,lincRNA intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1436652540 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1691111 RMVar_hsa_circ_119287,RMVar_hsa_circ_244878,RMVar_hsa_circ_98844,RMVar_hsa_circ_244877,RMVar_hsa_circ_31787,RMVar_hsa_circ_107215,RMVar_hsa_circ_116772,RMVar_hsa_circ_244883,RMVar_hsa_circ_244888,RMVar_hsa_circ_77569,RMVar_hsa_circ_101844,RMVar_hsa_circ_244889,RMVar_hsa_circ_116119,RMVar_hsa_circ_244891,RMVar_hsa_circ_244893 38696 RMVar_ID_38696 Human_SNP_ID_318687009 A-to-I Human chr7 - 44012674 44012674 44012674 ACTACTCAGAGGTCTGATGCAGGAGAATTGCTAAAACCCAGGAGGGAGAGGTTACATTGAGCCGA ACTACTCAGAGGTCTGATGCAGGAGAATTGCTGAAACCCAGGAGGGAGAGGTTACATTGAGCCGA T C AC017116.2,POLR2J4,AC004951.4 Ensembl:ENSG00000285596,Ensembl:ENSG00000214783,Ensembl:ENSG00000273432 lincRNA,lincRNA,lincRNA exon,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs3209192 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16159279 RMVar_hsa_circ_119287,RMVar_hsa_circ_244878,RMVar_hsa_circ_98844,RMVar_hsa_circ_244877,RMVar_hsa_circ_31787,RMVar_hsa_circ_107215,RMVar_hsa_circ_116772,RMVar_hsa_circ_244883,RMVar_hsa_circ_244888,RMVar_hsa_circ_77569,RMVar_hsa_circ_101844,RMVar_hsa_circ_244889,RMVar_hsa_circ_244891 38697 RMVar_ID_38697 Human_SNP_ID_318691680 A-to-I Human chr7 - 44031254 44031254 44031254 GTGAACCTGGGAGGCAGAGCTCGCAGTGAGCCAAGATCGTGCCACTGCACTGCAGCCTGCGCGAC GTGAACCTGGGAGGCAGAGCTCGCAGTGAGCCGAGATCGTGCCACTGCACTGCAGCCTGCGCGAC T C AC017116.2,RASA4CP Ensembl:ENSG00000285596,Ensembl:ENSG00000228903 lincRNA,Pseudogene intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1474746352 Functional Loss SNV dbSNP153 33..33 33 - - - 38698 RMVar_ID_38698 Human_SNP_ID_318691990 A-to-I Human chr7 - 44032637 44032637 44032637 GGGAGGCCAAGGTAGGCGGATTGCCTGAGCTCAGGAGTTAGAGACAAGCCTAGGCAACATGGTGA GGGAGGCCAAGGTAGGCGGATTGCCTGAGCTCTGGAGTTAGAGACAAGCCTAGGCAACATGGTGA T A AC017116.2,RASA4CP Ensembl:ENSG00000285596,Ensembl:ENSG00000228903 lincRNA,Pseudogene intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1387855458 Functional Loss SNV dbSNP153 33..33 33 - - - 38699 RMVar_ID_38699 Human_SNP_ID_318692316 A-to-I Human chr7 - 44033830 44033830 44033830 CAGACTGGAGTGCAATGGCACGATCTCAGCTCACTGCAATCTCCACCTCCCAGGGTCAAGCAATT CAGACTGGAGTGCAATGGCACGATCTCAGCTCGCTGCAATCTCCACCTCCCAGGGTCAAGCAATT T C AC017116.2,RASA4CP Ensembl:ENSG00000285596,Ensembl:ENSG00000228903 lincRNA,Pseudogene intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs778252058 Functional Loss SNV dbSNP153 33..33 33 - - - 38700 RMVar_ID_38700 Human_SNP_ID_318693123 A-to-I Human chr7 - 44036743 44036743 44036743 CAGCAGAAAAGGTTGAGGAAAAGAACTTTGGCAGCTCGCACGTCATGCAGGTCATCTACACGGAC CAGCAGAAAAGGTTGAGGAAAAGAACTTTGGCGGCTCGCACGTCATGCAGGTCATCTACACGGAC T C AC017116.2,RASA4CP Ensembl:ENSG00000285596,Ensembl:ENSG00000228903 lincRNA,Pseudogene exon,intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs759022262 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5623944 Human_Splice_Rec_861036,Human_Splice_Rec_861037,Human_Splice_Rec_861080,Human_Splice_Rec_861081 RMVar_hsa_circ_244897,RMVar_hsa_circ_116807 38701 RMVar_ID_38701 Human_SNP_ID_318694539 A-to-I Human chr7 + 44041652 44041652 44041652 GAACTCCTGACCTTAAGTGATCCGCCCGCCTCAGCCTCCCAAAGTGCTGGAATTACAGGCATGAG GAACTCCTGACCTTAAGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGAATTACAGGCATGAG A G LINC00957 Ensembl:ENSG00000235314 lincRNA exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1347319383 Functional Loss SNV dbSNP153 33..33 33 - - - 38702 RMVar_ID_38702 Human_SNP_ID_318694641 A-to-I Human chr7 + 44042075 44042075 44042075 TCACACCTGTAATCCCAGTACTTTGGGAGGCCAAGGTGGGCAGATCACGAGGTCAAGAGATCGAG TCACACCTGTAATCCCAGTACTTTGGGAGGCCCAGGTGGGCAGATCACGAGGTCAAGAGATCGAG A C LINC00957 Ensembl:ENSG00000235314 lincRNA exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1215056011 Functional Loss SNV dbSNP153 33..33 33 - - - 38703 RMVar_ID_38703 Human_SNP_ID_318698152 A-to-I Human chr7 + 44054427 44054427 44054427 GTTGGCCAGGCTGGTCTGGAATCCCTGAGCTCAAGTGATCTGCCCTCTTCAGCTTCCCAAAGTGC GTTGGCCAGGCTGGTCTGGAATCCCTGAGCTCTAGTGATCTGCCCTCTTCAGCTTCCCAAAGTGC A T DBNL Ensembl:ENSG00000136279 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs755213029 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16159568 RMVar_hsa_circ_85672,RMVar_hsa_circ_334923,RMVar_hsa_circ_367546,RMVar_hsa_circ_8823,RMVar_hsa_circ_30772,RMVar_hsa_circ_55730,RMVar_hsa_circ_244902 38704 RMVar_ID_38704 Human_SNP_ID_318702737 A-to-I Human chr7 - 44071777 44071777 44071777 AAAATACAAAAATTTGCTGGGCATGTTGGCTCATACCTGTATTCCCAGCTACACGGGAGGCTGAG AAAATACAAAAATTTGCTGGGCATGTTGGCTCGTACCTGTATTCCCAGCTACACGGGAGGCTGAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs951471124 Functional Loss SNV dbSNP153 33..33 33 - - - 38705 RMVar_ID_38705 Human_SNP_ID_318702738 A-to-I Human chr7 - 44071777 44071777 44071777 AAAATACAAAAATTTGCTGGGCATGTTGGCTCATACCTGTATTCCCAGCTACACGGGAGGCTGAG AAAATACAAAAATTTGCTGGGCATGTTGGCTCCTACCTGTATTCCCAGCTACACGGGAGGCTGAG T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs951471124 Functional Loss SNV dbSNP153 33..33 33 - - - 38706 RMVar_ID_38706 Human_SNP_ID_318702770 A-to-I Human chr7 - 44071903 44071903 44071903 GTTGTGGCCGGATGCCGTGGCTCATGCCTGTAATCCTAGCACTTTGGGAGGCTGAGACGGGTGGA GTTGTGGCCGGATGCCGTGGCTCATGCCTGTAGTCCTAGCACTTTGGGAGGCTGAGACGGGTGGA T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs906164161 Functional Loss SNV dbSNP153 33..33 33 - - - 38707 RMVar_ID_38707 Human_SNP_ID_318703876 A-to-I Human chr7 - 44075179 44075179 44075179 GGGTGTGGTGGCAGACACCCGTAATCTCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAA GGGTGTGGTGGCAGACACCCGTAATCTCAGCTGCTCGGGAGGCTGAGGCAGGAGAATCACTTGAA T C POLM Ensembl:ENSG00000122678 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs555933896 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18994 38708 RMVar_ID_38708 Human_SNP_ID_318704633 A-to-I Human chr7 - 44078270 44078270 44078270 TCGTAAAGATGGGGTCTTGGTAATGTTGCCTAAGCTGGTCTCAAACCCCTATGCTCAAATGATTC TCGTAAAGATGGGGTCTTGGTAATGTTGCCTATGCTGGTCTCAAACCCCTATGCTCAAATGATTC T A POLM Ensembl:ENSG00000122678 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs564848425 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_244909,RMVar_hsa_circ_100387,RMVar_hsa_circ_34282 38709 RMVar_ID_38709 Human_SNP_ID_318704651 A-to-I Human chr7 - 44078342 44078342 44078342 CCCACCTCAGTCTCTGGAGTAGCTGGGACTACAGGCATGTGCCACCACACCAGGTTAATTTTTAA CCCACCTCAGTCTCTGGAGTAGCTGGGACTACTGGCATGTGCCACCACACCAGGTTAATTTTTAA T A POLM Ensembl:ENSG00000122678 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs1394303344 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_861515 RMVar_hsa_circ_244909,RMVar_hsa_circ_100387,RMVar_hsa_circ_34282 38710 RMVar_ID_38710 Human_SNP_ID_318704663 A-to-I Human chr7 - 44078382 44078382 44078382 AGCTCACGGCAGCCTTGACTTCCTGGGCTCAAACCATCCTCCCACCTCAGTCTCTGGAGTAGCTG AGCTCACGGCAGCCTTGACTTCCTGGGCTCAATCCATCCTCCCACCTCAGTCTCTGGAGTAGCTG T A POLM Ensembl:ENSG00000122678 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs982324517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_861515 RMVar_hsa_circ_244909,RMVar_hsa_circ_100387,RMVar_hsa_circ_34282 38711 RMVar_ID_38711 Human_SNP_ID_318717034 A-to-I Human chr7 - 44122355 44122355 44122355 AGTTGTCCAGATGGAACAGGACACCTGAGTCTAGGGTTCGGGAAGAACTCCAGATGGGACAAACA AGTTGTCCAGATGGAACAGGACACCTGAGTCTGGGGTTCGGGAAGAACTCCAGATGGGACAAACA T C POLD2 Ensembl:ENSG00000106628 Protein coding intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1454784507 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16160052 Human_Splice_Rec_861745,Human_Splice_Rec_861871 RMVar_hsa_circ_126276,RMVar_hsa_circ_244922 38712 RMVar_ID_38712 Human_SNP_ID_318739984 A-to-I Human chr7 + 44214023 44214023 44214023 ACCTCTCCCTTTCCCACTTGAGGACCCTGGGGAGAGATGGGGGCGGGGAAAATGGAGGTATGAAT ACCTCTCCCTTTCCCACTTGAGGACCCTGGGGGGAGATGGGGGCGGGGAAAATGGAGGTATGAAT A G YKT6 Ensembl:ENSG00000106636 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1472640335 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_684555,Human_RBP_ID_7740774,Human_RBP_ID_17426937,Human_RBP_ID_17713118,Human_RBP_ID_18100687 Human_miRNA_ID_2256958 RMVar_hsa_circ_113965,RMVar_hsa_circ_244924,RMVar_hsa_circ_103139,RMVar_hsa_circ_244928 38713 RMVar_ID_38713 Human_SNP_ID_318740032 A-to-I Human chr7 + 44214155 44214155 44214155 ACTCAGGCCCTGTGAGATAGAGGGCCCAGCCCAGCCCCACCCACAGATCCCCTGCTCCTGTTGTG ACTCAGGCCCTGTGAGATAGAGGGCCCAGCCCGGCCCCACCCACAGATCCCCTGCTCCTGTTGTG A G YKT6 Ensembl:ENSG00000106636 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs576038415 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_684556,Human_RBP_ID_793225,Human_RBP_ID_4941688,Human_RBP_ID_8219593,Human_RBP_ID_24216306,Human_RBP_ID_26551268 Human_miRNA_ID_1705842,Human_miRNA_ID_2553353 RMVar_hsa_circ_113965,RMVar_hsa_circ_244924,RMVar_hsa_circ_103139,RMVar_hsa_circ_244928 38714 RMVar_ID_38714 Human_SNP_ID_318786933 A-to-I Human chr7 - 44403344 44403344 44403344 CTCACTCTCCTAGTGAGTGTTTCATCCTAAGCAGGGCCTCCTATTTAGGCCCTACGTGAGGCCCT CTCACTCTCCTAGTGAGTGTTTCATCCTAAGCGGGGCCTCCTATTTAGGCCCTACGTGAGGCCCT T C NUDCD3 Ensembl:ENSG00000015676 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1204040625 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6425,RMVar_hsa_circ_123718,RMVar_hsa_circ_278699,RMVar_hsa_circ_244935,RMVar_hsa_circ_95003,RMVar_hsa_circ_244936,RMVar_hsa_circ_244937,RMVar_hsa_circ_244938 38715 RMVar_ID_38715 Human_SNP_ID_318787621 A-to-I Human chr7 - 44406078 44406076 44406078 AACTATCTGATGGGCTGGATGTGGTGGCTCACATGTGTCATCCCAGCACTTTGGGAGGCTGAGGC AACTATCTGATGGGCTGGATGTGGTGGCTCAC__GTGTCATCCCAGCACTTTGGGAGGCTGAGGC CAT C NUDCD3 Ensembl:ENSG00000015676 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1261285204 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_6425,RMVar_hsa_circ_123718,RMVar_hsa_circ_244935,RMVar_hsa_circ_95003,RMVar_hsa_circ_102767,RMVar_hsa_circ_244937,RMVar_hsa_circ_244938,RMVar_hsa_circ_332426,RMVar_hsa_circ_353272,RMVar_hsa_circ_109365,RMVar_hsa_circ_244941,RMVar_hsa_circ_244942,RMVar_hsa_circ_244940 38716 RMVar_ID_38716 Human_SNP_ID_318787622 A-to-I Human chr7 - 44406078 44406078 44406078 AACTATCTGATGGGCTGGATGTGGTGGCTCACATGTGTCATCCCAGCACTTTGGGAGGCTGAGGC AACTATCTGATGGGCTGGATGTGGTGGCTCACGTGTGTCATCCCAGCACTTTGGGAGGCTGAGGC T C NUDCD3 Ensembl:ENSG00000015676 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs961192835 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6425,RMVar_hsa_circ_123718,RMVar_hsa_circ_244935,RMVar_hsa_circ_95003,RMVar_hsa_circ_102767,RMVar_hsa_circ_244937,RMVar_hsa_circ_244938,RMVar_hsa_circ_332426,RMVar_hsa_circ_353272,RMVar_hsa_circ_109365,RMVar_hsa_circ_244941,RMVar_hsa_circ_244942,RMVar_hsa_circ_244940 38717 RMVar_ID_38717 Human_SNP_ID_318789277 A-to-I Human chr7 - 44413240 44413240 44413240 CCCTGTGTTGTTCAGGCTGGTCTTAAACTCCTAGGCTCAAGTAATCCCCCTGCCTCAGACTCCCA CCCTGTGTTGTTCAGGCTGGTCTTAAACTCCTGGGCTCAAGTAATCCCCCTGCCTCAGACTCCCA T C NUDCD3 Ensembl:ENSG00000015676 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs958414585 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_862778,Human_Splice_Rec_862779 RMVar_hsa_circ_6425,RMVar_hsa_circ_123718,RMVar_hsa_circ_244935,RMVar_hsa_circ_95003,RMVar_hsa_circ_102767,RMVar_hsa_circ_244937,RMVar_hsa_circ_244938,RMVar_hsa_circ_332426,RMVar_hsa_circ_353272,RMVar_hsa_circ_109365,RMVar_hsa_circ_99998,RMVar_hsa_circ_244941,RMVar_hsa_circ_244942,RMVar_hsa_circ_244940,RMVar_hsa_circ_101442,RMVar_hsa_circ_244943,RMVar_hsa_circ_244944 38718 RMVar_ID_38718 Human_SNP_ID_318800547 A-to-I Human chr7 - 44461216 44461216 44461216 GGTCCAGACCCATTTTCTGGAATGTCAGAAATACTTCCTGGAGAAGGTGATGCCTGTGCTGGCCT GGTCCAGACCCATTTTCTGGAATGTCAGAAATGCTTCCTGGAGAAGGTGATGCCTGTGCTGGCCT T C NUDCD3 Ensembl:ENSG00000015676 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1294062736 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 38719 RMVar_ID_38719 Human_SNP_ID_318802172 A-to-I Human chr7 + 44467961 44467961 44467961 GATCGTCAAAAAGAGAACCAAGAAGTTCATCCAGCACCAGTCAGACCAATATGTCAAAATTAAGC GATCGTCAAAAAGAGAACCAAGAAGTTCATCCGGCACCAGTCAGACCAATATGTCAAAATTAAGC A G AC004453.1 Ensembl:ENSG00000146677 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs562719193 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1822365 38720 RMVar_ID_38720 Human_SNP_ID_318802179 A-to-I Human chr7 + 44467976 44467976 44467976 AACCAAGAAGTTCATCCAGCACCAGTCAGACCAATATGTCAAAATTAAGCGTAACTGGCGGAAAC AACCAAGAAGTTCATCCAGCACCAGTCAGACCGATATGTCAAAATTAAGCGTAACTGGCGGAAAC A G AC004453.1 Ensembl:ENSG00000146677 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs533465480 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_684637,Human_RBP_ID_1052116,Human_RBP_ID_9211327,Human_RBP_ID_17316391,Human_RBP_ID_18520218,Human_RBP_ID_24216503,Human_RBP_ID_26552290,Human_RBP_ID_27113864 38721 RMVar_ID_38721 Human_SNP_ID_318802280 A-to-I Human chr7 + 44468200 44468200 44468200 GCAACAAATCTTACTGTGCCGAGATCGCTCACAATGTTTCCTCCAAGAACCGCAAAGCCATCGTG GCAACAAATCTTACTGTGCCGAGATCGCTCACGATGTTTCCTCCAAGAACCGCAAAGCCATCGTG A G AC004453.1 Ensembl:ENSG00000146677 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1395163331 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_684641,Human_RBP_ID_1686900,Human_RBP_ID_2043276,Human_RBP_ID_3847306,Human_RBP_ID_8272234,Human_RBP_ID_9211328,Human_RBP_ID_17312962,Human_RBP_ID_17425519,Human_RBP_ID_17543530,Human_RBP_ID_18540572,Human_RBP_ID_26546866,Human_RBP_ID_26831284,Human_RBP_ID_27531784 Human_miRNA_ID_1873441,Human_miRNA_ID_1882294,Human_miRNA_ID_1909013 38722 RMVar_ID_38722 Human_SNP_ID_318823669 A-to-I Human chr7 - 44552321 44552321 44552321 CTCATCCCTCAGCCTTCCAAGTTACTGGGACTACAGGCACGTGCCACCATGCCTGGCGAATTTTT CTCATCCCTCAGCCTTCCAAGTTACTGGGACTGCAGGCACGTGCCACCATGCCTGGCGAATTTTT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1453432999 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7741431,Human_RBP_ID_16163230 38723 RMVar_ID_38723 Human_SNP_ID_318824500 A-to-I Human chr7 - 44555624 44555624 44555624 GTGATCCTCCTGTCTGAGCCTCCTGAGTAACTAGGACTACAGGCATGCACCACTACACCAAGATT GTGATCCTCCTGTCTGAGCCTCCTGAGTAACTGGGACTACAGGCATGCACCACTACACCAAGATT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1392427056 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16163340 38724 RMVar_ID_38724 Human_SNP_ID_318829863 A-to-I Human chr7 + 44574368 44574368 44574368 AATAATGAGCCATGGCAGCAACTGCCTGAGAGAGAGGACCGGCGGGTTGCTGTAGGGCTCCCTAA AATAATGAGCCATGGCAGCAACTGCCTGAGAGGGAGGACCGGCGGGTTGCTGTAGGGCTCCCTAA A G lnc-OGDH-5 RNACentral:URS00008B357A lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569377258 Functional Loss SNV dbSNP153 33..33 33 - - - 38725 RMVar_ID_38725 Human_SNP_ID_318830270 A-to-I Human chr7 + 44575845 44575845 44575845 ATTTTTAGTAGAGACAGGGTTTCACCGTTGTTAGCCAGGATGGTCTCGATCTCCTGACCTTGTGA ATTTTTAGTAGAGACAGGGTTTCACCGTTGTTGGCCAGGATGGTCTCGATCTCCTGACCTTGTGA A G NONHSAG047490.2 RNACentral:URS00009B0D60 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs549179407 Functional Loss SNV dbSNP153 33..33 33 - - - 38726 RMVar_ID_38726 Human_SNP_ID_318830287 A-to-I Human chr7 - 44575911 44575911 44575911 GTTAGGGCCTGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGG GTTAGGGCCTGGGCGCGGTGGCTCACGCCTGTGATCCCAGCACTTTGGGAGGCCGAGGCGGGCGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1562587375 Functional Loss SNV dbSNP153 33..33 33 - - - 38727 RMVar_ID_38727 Human_SNP_ID_318830595 A-to-I Human chr7 - 44576975 44576975 44576975 TAGTCCCAGCTACTTGAGAGGCTGAGGTGGAAAGATCACTTGAGCCCGGGAGGTCAAGGCTGCGG TAGTCCCAGCTACTTGAGAGGCTGAGGTGGAAGGATCACTTGAGCCCGGGAGGTCAAGGCTGCGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1269302562 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16164002 38728 RMVar_ID_38728 Human_SNP_ID_318830598 A-to-I Human chr7 - 44576996 44576996 44576996 TTAGCTGGTGGCACATGCCTATAGTCCCAGCTACTTGAGAGGCTGAGGTGGAAAGATCACTTGAG TTAGCTGGTGGCACATGCCTATAGTCCCAGCTGCTTGAGAGGCTGAGGTGGAAAGATCACTTGAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1469313410 Functional Loss SNV dbSNP153 33..33 33 - - - 38729 RMVar_ID_38729 Human_SNP_ID_318830602 A-to-I Human chr7 - 44577008 44577008 44577008 AATACAAAAAATTTAGCTGGTGGCACATGCCTATAGTCCCAGCTACTTGAGAGGCTGAGGTGGAA AATACAAAAAATTTAGCTGGTGGCACATGCCTGTAGTCCCAGCTACTTGAGAGGCTGAGGTGGAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs537246394 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26105261 38730 RMVar_ID_38730 Human_SNP_ID_318830649 A-to-I Human chr7 + 44577242 44577242 44577242 CCTGTAGTACCAGCTACTTGGGAGGGTAAGGTAGGAGGATCACTTGAACCTGGGAGCTCAAGGTT CCTGTAGTACCAGCTACTTGGGAGGGTAAGGTGGGAGGATCACTTGAACCTGGGAGCTCAAGGTT A G NONHSAG047490.2 RNACentral:URS00009B0D60 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1001150654 Functional Loss SNV dbSNP153 33..33 33 - - - 38731 RMVar_ID_38731 Human_SNP_ID_318830682 A-to-I Human chr7 - 44577373 44577373 44577373 TCCTGACCGCAGGTGACCCGTCTCGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCTGGCCGGG TCCTGACCGCAGGTGACCCGTCTCGCCTCCCAGAGTGCTGGGATTACAGGTGTGAGCTGGCCGGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs911900300 Functional Loss SNV dbSNP153 33..33 33 - - - 38732 RMVar_ID_38732 Human_SNP_ID_318830773 A-to-I Human chr7 - 44577667 44577667 44577667 CTTCTGAGTAGCTGGGATTACAGACACCCACCACTACACCCGGCTAATTTTTGTATTTTTATTTT CTTCTGAGTAGCTGGGATTACAGACACCCACCGCTACACCCGGCTAATTTTTGTATTTTTATTTT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1171268816 Functional Loss SNV dbSNP153 33..33 33 - - - 38733 RMVar_ID_38733 Human_SNP_ID_318831035 A-to-I Human chr7 - 44578782 44578782 44578782 GCTCACTGGCAACATCTGCCTCCCGGGTTCAAATGATTCTCCTGCCTCAGTCTCCTGAGTAGCTG GCTCACTGGCAACATCTGCCTCCCGGGTTCAAGTGATTCTCCTGCCTCAGTCTCCTGAGTAGCTG T C TMED4 Ensembl:ENSG00000158604 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1134360 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_684732,Human_RBP_ID_8667812,Human_RBP_ID_16164067,Human_RBP_ID_17312977,Human_RBP_ID_18382460,Human_RBP_ID_26105298,Human_RBP_ID_26546910 Human_miRNA_ID_1789486 38734 RMVar_ID_38734 Human_SNP_ID_318831045 A-to-I Human chr7 - 44578828 44578828 44578828 AGTTTTGCTCTTGTCGCCCAGGCTGGAGTGCAATGGCGTGATCTCAGCTCACTGGCAACATCTGC AGTTTTGCTCTTGTCGCCCAGGCTGGAGTGCAGTGGCGTGATCTCAGCTCACTGGCAACATCTGC T C TMED4 Ensembl:ENSG00000158604 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs17404280 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_684732,Human_RBP_ID_794847,Human_RBP_ID_9211355,Human_RBP_ID_16164068,Human_RBP_ID_17541426,Human_RBP_ID_26105301 Human_miRNA_ID_507034,Human_miRNA_ID_1077339,Human_miRNA_ID_1389735 38735 RMVar_ID_38735 Human_SNP_ID_318831057 A-to-I Human chr7 - 44578860 44578860 44578860 TTTTTCCTTTTTTTTTTTTTTTTTTTTTTTTGAGTTTTGCTCTTGTCGCCCAGGCTGGAGTGCAA TTTTTCCTTTTTTTTTTTTTTTTTTTTTTTTGTGTTTTGCTCTTGTCGCCCAGGCTGGAGTGCAA T A TMED4 Ensembl:ENSG00000158604 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1329220429 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_684732,Human_RBP_ID_7741781,Human_RBP_ID_16164076 Human_miRNA_ID_1103356 38736 RMVar_ID_38736 Human_SNP_ID_318831331 A-to-I Human chr7 + 44579931 44579929 44579931 GATTGTGAACTGTCCTTTCTTCATTTTATTTTATAGAGCTTAAAAATGACTACTGAAAGCGAAAT GATTGTGAACTGTCCTTTCTTCATTTTATTT__TAGAGCTTAAAAATGACTACTGAAAGCGAAAT TTA T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1392023473 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_3847428,Human_RBP_ID_7741819 38737 RMVar_ID_38737 Human_SNP_ID_318831395 A-to-I Human chr7 - 44580235 44580235 44580235 GGCCTCAGGCAATCCACTGCCGCAGCCTCCCAAAGTGTTGGGATTACAGGCGTGAGCCACTGCAC GGCCTCAGGCAATCCACTGCCGCAGCCTCCCATAGTGTTGGGATTACAGGCGTGAGCCACTGCAC T A TMED4 Ensembl:ENSG00000158604 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1469846472 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9211365,Human_RBP_ID_23077065,Human_RBP_ID_26138063 38738 RMVar_ID_38738 Human_SNP_ID_318831397 A-to-I Human chr7 - 44580244 44580242 44580244 TGAACTCCTGGCCTCAGGCAATCCACTGCCGCAGCCTCCCAAAGTGTTGGGATTACAGGCGTGAG TGAACTCCTGGCCTCAGGCAATCCACTGCCGC__CCTCCCAAAGTGTTGGGATTACAGGCGTGAG GCT G TMED4 Ensembl:ENSG00000158604 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1562590100 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_9211365,Human_RBP_ID_16164166,Human_RBP_ID_26772145 Human_miRNA_ID_1397584 38739 RMVar_ID_38739 Human_SNP_ID_318831402 A-to-I Human chr7 - 44580256 44580256 44580256 CCAGGCTGGTCTTGAACTCCTGGCCTCAGGCAATCCACTGCCGCAGCCTCCCAAAGTGTTGGGAT CCAGGCTGGTCTTGAACTCCTGGCCTCAGGCAGTCCACTGCCGCAGCCTCCCAAAGTGTTGGGAT T C TMED4 Ensembl:ENSG00000158604 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs923916930 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9211365,Human_RBP_ID_16164166,Human_RBP_ID_26772145 38740 RMVar_ID_38740 Human_SNP_ID_318831544 A-to-I Human chr7 - 44580725 44580725 44580725 TCAGGCTGGTCTCGAACTCCCGACATCAAGTGATCCGCCCGCCTCAGCCTCCCAAAGTGCTGGGA TCAGGCTGGTCTCGAACTCCCGACATCAAGTGGTCCGCCCGCCTCAGCCTCCCAAAGTGCTGGGA T C TMED4 Ensembl:ENSG00000158604 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879056913 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10354544,Human_RBP_ID_26105331 38741 RMVar_ID_38741 Human_SNP_ID_318831610 A-to-I Human chr7 - 44580935 44580929 44580936 TTGTTTGTTTGTTGTTTTTGAGACGGAGTTTCACTCTTGTTGCCCATGCTGGAGTGCAATGCCAT TTGTTTGTTTGTTGTTTTTGAGACGGAGTTT_______GTTGCCCATGCTGGAGTGCAATGCCAT CAAGAGTG C TMED4 Ensembl:ENSG00000158604 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1293733779 Functional Loss DEL dbSNP153 32..38 33 - - - Human_RBP_ID_3847434,Human_RBP_ID_16164182 38742 RMVar_ID_38742 Human_SNP_ID_318831613 A-to-I Human chr7 - 44580941 44580941 44580941 GATAGGTTGTTTGTTTGTTGTTTTTGAGACGGAGTTTCACTCTTGTTGCCCATGCTGGAGTGCAA GATAGGTTGTTTGTTTGTTGTTTTTGAGACGGGGTTTCACTCTTGTTGCCCATGCTGGAGTGCAA T C TMED4 Ensembl:ENSG00000158604 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1489570712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3847434,Human_RBP_ID_7788352,Human_RBP_ID_8667823,Human_RBP_ID_16164182 38743 RMVar_ID_38743 Human_SNP_ID_318839161 A-to-I Human chr7 + 44610055 44610055 44610055 CCAGGCTGGTCTTGAACTCCTGGGATCAAGTGATCCTCCTGTCTTAGCCTCCCAAAGGCTAGGAT CCAGGCTGGTCTTGAACTCCTGGGATCAAGTGGTCCTCCTGTCTTAGCCTCCCAAAGGCTAGGAT A G OGDH Ensembl:ENSG00000105953 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs536334243 Functional Loss SNV dbSNP153 33..33 33 - - - 38744 RMVar_ID_38744 Human_SNP_ID_318842446 A-to-I Human chr7 + 44621274 44621274 44621274 TTTTAAATTTTTTGTGGAGATGTGGTTTCACTATGTTGCCCGGGCTGGTCTCAAACTCCTGGCCT TTTTAAATTTTTTGTGGAGATGTGGTTTCACTGTGTTGCCCGGGCTGGTCTCAAACTCCTGGCCT A G OGDH Ensembl:ENSG00000105953 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037642495 Functional Loss SNV dbSNP153 33..33 33 - - - 38745 RMVar_ID_38745 Human_SNP_ID_318844373 A-to-I Human chr7 + 44628697 44628697 44628697 GTCTTGAACTCCTGGGCTCAAGCAATCCTCCCAGCTTGGCCTCCCAAAGTGCTGGGATTACAGAT GTCTTGAACTCCTGGGCTCAAGCAATCCTCCCTGCTTGGCCTCCCAAAGTGCTGGGATTACAGAT A T OGDH Ensembl:ENSG00000105953 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1386473205 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33602,RMVar_hsa_circ_308864,RMVar_hsa_circ_313746,RMVar_hsa_circ_344339,RMVar_hsa_circ_92710,RMVar_hsa_circ_102585,RMVar_hsa_circ_36246,RMVar_hsa_circ_244970,RMVar_hsa_circ_244972,RMVar_hsa_circ_244973,RMVar_hsa_circ_244971 38746 RMVar_ID_38746 Human_SNP_ID_318852227 A-to-I Human chr7 + 44660891 44660891 44660891 TTAAGGCTGCAGTGATCTATGATTGCACCACTATACTCTGGCCTGGGTGACCCTATCTGTAAACT TTAAGGCTGCAGTGATCTATGATTGCACCACTGTACTCTGGCCTGGGTGACCCTATCTGTAAACT A G OGDH Ensembl:ENSG00000105953 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs958072848 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16165013 RMVar_hsa_circ_77643,RMVar_hsa_circ_33602,RMVar_hsa_circ_92710,RMVar_hsa_circ_102585,RMVar_hsa_circ_36246,RMVar_hsa_circ_119943,RMVar_hsa_circ_286028,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_244979,RMVar_hsa_circ_299727,RMVar_hsa_circ_29218,RMVar_hsa_circ_244984,RMVar_hsa_circ_337603,RMVar_hsa_circ_273431,RMVar_hsa_circ_244985 38747 RMVar_ID_38747 Human_SNP_ID_318852834 A-to-I Human chr7 + 44663408 44663408 44663408 GCCTGTAAGCACTTTGGGAGACCAAGGCAGGCAGATTGCTTGAGCTCAGGAGTTCGAGACCAGCC GCCTGTAAGCACTTTGGGAGACCAAGGCAGGCGGATTGCTTGAGCTCAGGAGTTCGAGACCAGCC A G OGDH Ensembl:ENSG00000105953 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432807903 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24389711 RMVar_hsa_circ_77643,RMVar_hsa_circ_33602,RMVar_hsa_circ_92710,RMVar_hsa_circ_102585,RMVar_hsa_circ_36246,RMVar_hsa_circ_119943,RMVar_hsa_circ_286028,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_244979,RMVar_hsa_circ_299727,RMVar_hsa_circ_29218,RMVar_hsa_circ_244984,RMVar_hsa_circ_337603,RMVar_hsa_circ_273431,RMVar_hsa_circ_244985 38748 RMVar_ID_38748 Human_SNP_ID_318860945 A-to-I Human chr7 + 44695157 44695157 44695157 TAGCTCTGTCACCCAGGCTGGAGTGCCGTGGCATGATCTTAGCTCACTGCAACCTCCACCTCCTT TAGCTCTGTCACCCAGGCTGGAGTGCCGTGGCGTGATCTTAGCTCACTGCAACCTCCACCTCCTT A G OGDH Ensembl:ENSG00000105953 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1354715816 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92710,RMVar_hsa_circ_119943,RMVar_hsa_circ_244970,RMVar_hsa_circ_123357,RMVar_hsa_circ_244982,RMVar_hsa_circ_244983,RMVar_hsa_circ_118598,RMVar_hsa_circ_244988,RMVar_hsa_circ_90501,RMVar_hsa_circ_113468,RMVar_hsa_circ_114476,RMVar_hsa_circ_244995,RMVar_hsa_circ_22610,RMVar_hsa_circ_244996,RMVar_hsa_circ_354045,RMVar_hsa_circ_244997,RMVar_hsa_circ_244998,RMVar_hsa_circ_98044,RMVar_hsa_circ_245001 38749 RMVar_ID_38749 Human_SNP_ID_318863129 A-to-I Human chr7 + 44703232 44703232 44703232 GAGGTCACAAGTTTGAGACGAGCCTGGCCAACAGGGTGAAACCCCGTCTCTATTAAAAATACAAA GAGGTCACAAGTTTGAGACGAGCCTGGCCAACCGGGTGAAACCCCGTCTCTATTAAAAATACAAA A C OGDH Ensembl:ENSG00000105953 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs545113410 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_46823 38750 RMVar_ID_38750 Human_SNP_ID_318863130 A-to-I Human chr7 + 44703232 44703232 44703232 GAGGTCACAAGTTTGAGACGAGCCTGGCCAACAGGGTGAAACCCCGTCTCTATTAAAAATACAAA GAGGTCACAAGTTTGAGACGAGCCTGGCCAACTGGGTGAAACCCCGTCTCTATTAAAAATACAAA A T OGDH Ensembl:ENSG00000105953 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs545113410 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_46823 38751 RMVar_ID_38751 Human_SNP_ID_318863165 A-to-I Human chr7 + 44703365 44703365 44703365 GGGAGGCAGAGGTTGCAGTGAGCTGAGATTGCACCACTGCACTACAGCCTGGGCAACAGAGTAGG GGGAGGCAGAGGTTGCAGTGAGCTGAGATTGCGCCACTGCACTACAGCCTGGGCAACAGAGTAGG A G OGDH Ensembl:ENSG00000105953 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs567430497 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23315753 RMVar_hsa_circ_46823 38752 RMVar_ID_38752 Human_SNP_ID_318863166 A-to-I Human chr7 + 44703365 44703365 44703365 GGGAGGCAGAGGTTGCAGTGAGCTGAGATTGCACCACTGCACTACAGCCTGGGCAACAGAGTAGG GGGAGGCAGAGGTTGCAGTGAGCTGAGATTGCTCCACTGCACTACAGCCTGGGCAACAGAGTAGG A T OGDH Ensembl:ENSG00000105953 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs567430497 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23315753 RMVar_hsa_circ_46823 38753 RMVar_ID_38753 Human_SNP_ID_318863761 A-to-I Human chr7 + 44705572 44705571 44705573 TTTTTTATTTTTTGTTTGTGTTTTTTTGAGACAGAGTCTCACTCTGTCATCCAGGCTGATGCAAT TTTTTTATTTTTTGTTTGTGTTTTTTTGAGAC__AGTCTCACTCTGTCATCCAGGCTGATGCAAT CAG C OGDH Ensembl:ENSG00000105953 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs945889000 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_46823 38754 RMVar_ID_38754 Human_SNP_ID_318863762 A-to-I Human chr7 + 44705572 44705572 44705572 TTTTTTATTTTTTGTTTGTGTTTTTTTGAGACAGAGTCTCACTCTGTCATCCAGGCTGATGCAAT TTTTTTATTTTTTGTTTGTGTTTTTTTGAGACGGAGTCTCACTCTGTCATCCAGGCTGATGCAAT A G OGDH Ensembl:ENSG00000105953 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs981940597 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_46823 38755 RMVar_ID_38755 Human_SNP_ID_318875273 A-to-I Human chr7 + 44751949 44751949 44751949 GTGCCACTGCACTCCAGCCTCGGTGAAAGAGCAAGATTCCATCTCAAAAAGAAAAAAAAAAAATT GTGCCACTGCACTCCAGCCTCGGTGAAAGAGCCAGATTCCATCTCAAAAAGAAAAAAAAAAAATT A C ZMIZ2 Ensembl:ENSG00000122515 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917936936 Functional Loss SNV dbSNP153 33..33 33 - - - 38756 RMVar_ID_38756 Human_SNP_ID_318876235 A-to-I Human chr7 + 44756210 44756210 44756210 TGTCGGGCAGCCAGAGCAGCTGAGTTCCAGATAAAAACTGTCAGACCCGGCCTGTAGGCTGCTCC TGTCGGGCAGCCAGAGCAGCTGAGTTCCAGATGAAAACTGTCAGACCCGGCCTGTAGGCTGCTCC A G ZMIZ2 Ensembl:ENSG00000122515 Protein coding 5'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs758373887 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4942240 Human_Splice_Rec_863474,Human_Splice_Rec_863475,Human_Splice_Rec_863508,Human_Splice_Rec_863509,Human_Splice_Rec_863548,Human_Splice_Rec_863549,Human_Splice_Rec_863554,Human_Splice_Rec_863555,Human_Splice_Rec_863561,Human_Splice_Rec_863595,Human_Splice_Rec_863597,Human_Splice_Rec_863631,Human_Splice_Rec_863663 RMVar_hsa_circ_346,RMVar_hsa_circ_73459 38757 RMVar_ID_38757 Human_SNP_ID_318881388 A-to-I Human chr7 + 44772954 44772954 44772954 CTCACTGCAGCGTTGACCTCCAGGGCATAAGCACTCCTCTCATCTCAGCCTCCCAGGTGGCTGGG CTCACTGCAGCGTTGACCTCCAGGGCATAAGCCCTCCTCTCATCTCAGCCTCCCAGGTGGCTGGG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs570998655 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27357806 38758 RMVar_ID_38758 Human_SNP_ID_318881532 A-to-I Human chr7 + 44773425 44773425 44773425 AAAGTAATGCAATGGCAAGTGCAGTGGCTCACACCTGTAATCCGAGCACTTTGTGAAGTCAAGGC AAAGTAATGCAATGGCAAGTGCAGTGGCTCACGCCTGTAATCCGAGCACTTTGTGAAGTCAAGGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005119594 Functional Loss SNV dbSNP153 33..33 33 - - - 38759 RMVar_ID_38759 Human_SNP_ID_318886678 A-to-I Human chr7 - 44794492 44794492 44794492 GGAGTGCAGTGGTGCAATCCTAGCTCACTGTAACCTCGAACTCTTGGACTGAAGCATTCCTCCCT GGAGTGCAGTGGTGCAATCCTAGCTCACTGTAGCCTCGAACTCTTGGACTGAAGCATTCCTCCCT T C lnc-H2AFV-4 RNACentral:URS0000D5E2F9 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1482034120 Functional Loss SNV dbSNP153 33..33 33 - - - 38760 RMVar_ID_38760 Human_SNP_ID_318888638 A-to-I Human chr7 + 44800542 44800542 44800542 TCTGCCTCAGCCTCTCAAGTAGCTGGAACTACAGGCATGCACCACCACTCCCAGCTAAATTGTGT TCTGCCTCAGCCTCTCAAGTAGCTGGAACTACTGGCATGCACCACCACTCCCAGCTAAATTGTGT A T PPIA Ensembl:ENSG00000196262 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs533375328 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_794022,Human_RBP_ID_23077137 RMVar_hsa_circ_109340,RMVar_hsa_circ_90478,RMVar_hsa_circ_86560,RMVar_hsa_circ_245007,RMVar_hsa_circ_245010,RMVar_hsa_circ_99390,RMVar_hsa_circ_245011,RMVar_hsa_circ_106187,RMVar_hsa_circ_245013,RMVar_hsa_circ_245014 38761 RMVar_ID_38761 Human_SNP_ID_318889180 A-to-I Human chr7 + 44801890 44801890 44801890 AGGGTAGGAGTCAAGATCAGCCTGGGCAACATAGTGAGACGCTGTCTCTACAAAAAATAATTAGC AGGGTAGGAGTCAAGATCAGCCTGGGCAACATGGTGAGACGCTGTCTCTACAAAAAATAATTAGC A G PPIA Ensembl:ENSG00000196262 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs11547708 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26550483 RMVar_hsa_circ_109340,RMVar_hsa_circ_90478,RMVar_hsa_circ_86560,RMVar_hsa_circ_245007,RMVar_hsa_circ_245010,RMVar_hsa_circ_99390,RMVar_hsa_circ_245011,RMVar_hsa_circ_106187,RMVar_hsa_circ_245013,RMVar_hsa_circ_112819,RMVar_hsa_circ_245014,RMVar_hsa_circ_245016 38762 RMVar_ID_38762 Human_SNP_ID_318889191 A-to-I Human chr7 + 44801920 44801920 44801920 ATAGTGAGACGCTGTCTCTACAAAAAATAATTAGCCTGGCCTGGTGGTGCATGCCTAGTCCTAGC ATAGTGAGACGCTGTCTCTACAAAAAATAATTCGCCTGGCCTGGTGGTGCATGCCTAGTCCTAGC A C PPIA Ensembl:ENSG00000196262 Protein coding 3'UTR GSE38233;GSE100210;GSE99789;GSE107867;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;ASD brains,frontal_cortex;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,29796672,30559470,31158229,32596459 RNA-Seq:(High) rs1562773306 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8667969,Human_RBP_ID_18100977,Human_RBP_ID_18382494,Human_RBP_ID_26547005 Human_miRNA_ID_2753402,Human_miRNA_ID_2755336,Human_miRNA_ID_3120553 RMVar_hsa_circ_109340,RMVar_hsa_circ_90478,RMVar_hsa_circ_86560,RMVar_hsa_circ_245007,RMVar_hsa_circ_245010,RMVar_hsa_circ_99390,RMVar_hsa_circ_245011,RMVar_hsa_circ_106187,RMVar_hsa_circ_245013,RMVar_hsa_circ_112819,RMVar_hsa_circ_245014,RMVar_hsa_circ_245016 38763 RMVar_ID_38763 Human_SNP_ID_318889210 A-to-I Human chr7 + 44802000 44802000 44802000 CGTGGGAGGATTGCTTGAGCCTAGAGTGAGCTATTATCATGCCACTGTACAGCCTGGGTGTTCAC CGTGGGAGGATTGCTTGAGCCTAGAGTGAGCTGTTATCATGCCACTGTACAGCCTGGGTGTTCAC A G PPIA Ensembl:ENSG00000196262 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037618214 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_684890,Human_RBP_ID_7742236,Human_RBP_ID_8667970,Human_RBP_ID_24216843,Human_RBP_ID_26550484 RMVar_hsa_circ_109340,RMVar_hsa_circ_90478,RMVar_hsa_circ_86560,RMVar_hsa_circ_245007,RMVar_hsa_circ_245010,RMVar_hsa_circ_99390,RMVar_hsa_circ_245011,RMVar_hsa_circ_106187,RMVar_hsa_circ_245013,RMVar_hsa_circ_112819,RMVar_hsa_circ_245014,RMVar_hsa_circ_245016 38764 RMVar_ID_38764 Human_SNP_ID_318891022 A-to-I Human chr7 - 44807870 44807870 44807870 AAATTAGCTGGGCATGGTGGTGCCTCCCAGCTACTTGGCAGGCTGTGGCAGGAGAATCACTTGAA AAATTAGCTGGGCATGGTGGTGCCTCCCAGCTGCTTGGCAGGCTGTGGCAGGAGAATCACTTGAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1205068826 Functional Loss SNV dbSNP153 33..33 33 - - - 38765 RMVar_ID_38765 Human_SNP_ID_318896277 A-to-I Human chr7 - 44827327 44827327 44827327 GGAGCTAACCTCCACAGATGCTGATAGTCTGTAGAGTCAGGAATACCATGTAACATGTTGAAGTA GGAGCTAACCTCCACAGATGCTGATAGTCTGTGGAGTCAGGAATACCATGTAACATGTTGAAGTA T C H2AZ2 Ensembl:ENSG00000105968 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs11544539 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_684935,Human_RBP_ID_1687159,Human_RBP_ID_2043528,Human_RBP_ID_3847625,Human_RBP_ID_7742369,Human_RBP_ID_8668004,Human_RBP_ID_8911081,Human_RBP_ID_9211401,Human_RBP_ID_16165963,Human_RBP_ID_17313021,Human_RBP_ID_18382520,Human_RBP_ID_18883344,Human_RBP_ID_21508155 Human_miRNA_ID_277351,Human_miRNA_ID_2453741 RMVar_hsa_circ_116558,RMVar_hsa_circ_245017 38766 RMVar_ID_38766 Human_SNP_ID_318896651 A-to-I Human chr7 - 44829136 44829136 44829136 GATGTACAAGAGAGGTTCCAGGAGGGGGTGATAGGCAGAATTTTGGTCCCCATCACCTTCCCTGC GATGTACAAGAGAGGTTCCAGGAGGGGGTGATTGGCAGAATTTTGGTCCCCATCACCTTCCCTGC T A H2AZ2 Ensembl:ENSG00000105968 Protein coding 3'UTR GSE112787;GSE107867 293 Flip-In T-REx cells,empty vector;ASD brains,temporal_cortex - 29967493,30559470 RNA-Seq:(High) rs1413914116 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4942521,Human_RBP_ID_7742425,Human_RBP_ID_8911127,Human_RBP_ID_16166070,Human_RBP_ID_24216914 Human_miRNA_ID_1362844 RMVar_hsa_circ_116558,RMVar_hsa_circ_245017 38767 RMVar_ID_38767 Human_SNP_ID_318897088 A-to-I Human chr7 - 44830908 44830908 44830908 CTTGGCTCACTGCAACCTCAGCCTCCCAGGCAACTGGGACTACAGGCATGCGCCACCATGCCCAG CTTGGCTCACTGCAACCTCAGCCTCCCAGGCAGCTGGGACTACAGGCATGCGCCACCATGCCCAG T C H2AZ2 Ensembl:ENSG00000105968 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1486387060 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7742495,Human_RBP_ID_16166156,Human_RBP_ID_17313049 RMVar_hsa_circ_116558,RMVar_hsa_circ_245017 38768 RMVar_ID_38768 Human_SNP_ID_318897142 A-to-I Human chr7 - 44831153 44831153 44831153 TATTTTATTTTTATTTTTTCAGACAAAGTATTACTCTGTCGCCCAGGCTGGCATGCAGTGGCACA TATTTTATTTTTATTTTTTCAGACAAAGTATTTCTCTGTCGCCCAGGCTGGCATGCAGTGGCACA T A H2AZ2 Ensembl:ENSG00000105968 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1246514354 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4942588,Human_RBP_ID_7742501,Human_RBP_ID_8911168,Human_RBP_ID_16166167,Human_RBP_ID_17541491,Human_RBP_ID_24516641,Human_RBP_ID_27357844,Human_RBP_ID_27768662 RMVar_hsa_circ_116558,RMVar_hsa_circ_245017 38769 RMVar_ID_38769 Human_SNP_ID_318897523 A-to-I Human chr7 - 44832701 44832701 44832701 CAAGCCATCCTCCCACCTTGGCCTCCCAAAGTACTGGGATTATAGGCATAAGCCACCATGCCCTG CAAGCCATCCTCCCACCTTGGCCTCCCAAAGTGCTGGGATTATAGGCATAAGCCACCATGCCCTG T C H2AZ2 Ensembl:ENSG00000105968 Protein coding intron GSE100210;GSE112787 HepG2 cell line;293 Flip-In T-REx cells,empty vector - 29129909,29967493 RNA-Seq:(High) rs1133201 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116558,RMVar_hsa_circ_245017 38770 RMVar_ID_38770 Human_SNP_ID_318897524 A-to-I Human chr7 - 44832704 44832704 44832704 GCTCAAGCCATCCTCCCACCTTGGCCTCCCAAAGTACTGGGATTATAGGCATAAGCCACCATGCC GCTCAAGCCATCCTCCCACCTTGGCCTCCCAAGGTACTGGGATTATAGGCATAAGCCACCATGCC T C H2AZ2 Ensembl:ENSG00000105968 Protein coding intron GSE47997;GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,29129909,29796672,31158229,31158229,31158229,32596459,32596459 RNA-Seq:(High) rs1326053574 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116558,RMVar_hsa_circ_245017 38771 RMVar_ID_38771 Human_SNP_ID_318897539 A-to-I Human chr7 - 44832775 44832773 44832775 TGGCTAATTTTTTTTATTTATGTAAGAGACAGAGGTCTCCCTATGTTGCCCAGGTTGGTATTGAA TGGCTAATTTTTTTTATTTATGTAAGAGACAG__GTCTCCCTATGTTGCCCAGGTTGGTATTGAA CCT C H2AZ2 Ensembl:ENSG00000105968 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917277312 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_13797,Human_RBP_ID_17577391,Human_RBP_ID_23197868,Human_RBP_ID_24216960,Human_RBP_ID_26550500 RMVar_hsa_circ_116558,RMVar_hsa_circ_245017 38772 RMVar_ID_38772 Human_SNP_ID_318897540 A-to-I Human chr7 - 44832779 44832779 44832779 TACCTGGCTAATTTTTTTTATTTATGTAAGAGACAGAGGTCTCCCTATGTTGCCCAGGTTGGTAT TACCTGGCTAATTTTTTTTATTTATGTAAGAGGCAGAGGTCTCCCTATGTTGCCCAGGTTGGTAT T C H2AZ2 Ensembl:ENSG00000105968 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1464720634 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13797,Human_RBP_ID_17577391,Human_RBP_ID_18101063,Human_RBP_ID_23197868,Human_RBP_ID_24216960,Human_RBP_ID_26550500 RMVar_hsa_circ_116558,RMVar_hsa_circ_245017 38773 RMVar_ID_38773 Human_SNP_ID_318897549 A-to-I Human chr7 - 44832812 44832812 44832812 GCAAATAGCTGGGACCACAGGCACATGCCACCATACCTGGCTAATTTTTTTTATTTATGTAAGAG GCAAATAGCTGGGACCACAGGCACATGCCACCGTACCTGGCTAATTTTTTTTATTTATGTAAGAG T C H2AZ2 Ensembl:ENSG00000105968 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1340016469 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116558,RMVar_hsa_circ_245017 38774 RMVar_ID_38774 Human_SNP_ID_318897551 A-to-I Human chr7 - 44832815 44832814 44832815 CCTGCAAATAGCTGGGACCACAGGCACATGCCACCATACCTGGCTAATTTTTTTTATTTATGTAA CCTGCAAATAGCTGGGACCACAGGCACATGCC_CCATACCTGGCTAATTTTTTTTATTTATGTAA GT G H2AZ2 Ensembl:ENSG00000105968 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1421797372 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_116558,RMVar_hsa_circ_245017 38775 RMVar_ID_38775 Human_SNP_ID_318897554 A-to-I Human chr7 - 44832828 44832828 44832828 CTCTTACCTCAGCCCTGCAAATAGCTGGGACCACAGGCACATGCCACCATACCTGGCTAATTTTT CTCTTACCTCAGCCCTGCAAATAGCTGGGACCGCAGGCACATGCCACCATACCTGGCTAATTTTT T C H2AZ2 Ensembl:ENSG00000105968 Protein coding intron GSE47997;GSE38233;GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;ASD brains,temporal_cortex;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,29129909,30559470,31158229,31158229,31158229,32596459,32596459 RNA-Seq:(High) rs1175571837 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26547145 RMVar_hsa_circ_116558,RMVar_hsa_circ_245017 38776 RMVar_ID_38776 Human_SNP_ID_318897561 A-to-I Human chr7 - 44832863 44832863 44832863 TCACTGCAGCCTCCACCTCTCAGGCCCAAGCAATCCTCTTACCTCAGCCCTGCAAATAGCTGGGA TCACTGCAGCCTCCACCTCTCAGGCCCAAGCAGTCCTCTTACCTCAGCCCTGCAAATAGCTGGGA T C H2AZ2 Ensembl:ENSG00000105968 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs930829032 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26547146 RMVar_hsa_circ_116558,RMVar_hsa_circ_245017 38777 RMVar_ID_38777 Human_SNP_ID_318897578 A-to-I Human chr7 - 44832924 44832924 44832924 TTGTTTTGAGACAGGCTCTTGCTCTTTTGCCCAGGTTGAAGTGCAGTGGCATGATCCTGGCTCAC TTGTTTTGAGACAGGCTCTTGCTCTTTTGCCCGGGTTGAAGTGCAGTGGCATGATCCTGGCTCAC T C H2AZ2 Ensembl:ENSG00000105968 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900868578 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16166246,Human_RBP_ID_17577392,Human_RBP_ID_26547149 RMVar_hsa_circ_116558,RMVar_hsa_circ_245017 38778 RMVar_ID_38778 Human_SNP_ID_318897625 A-to-I Human chr7 - 44833115 44833115 44833115 TGAACCCAGGAGGCAGAGGTTGCAGTGAGCCAAGATCACGCCACTACACTCCAGCCTAGGTGACA TGAACCCAGGAGGCAGAGGTTGCAGTGAGCCAGGATCACGCCACTACACTCCAGCCTAGGTGACA T C H2AZ2 Ensembl:ENSG00000105968 Protein coding intron GSE38233;GSE112787;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;293 Flip-In T-REx cells,empty vector;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29967493,32596459 RNA-Seq:(High) rs1391937205 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116558,RMVar_hsa_circ_245017 38779 RMVar_ID_38779 Human_SNP_ID_318897660 A-to-I Human chr7 - 44833248 44833243 44833248 AGCTTGGCGACTGAGCAAGACTCCCTCTCAAAACAAACAAAAAAAAGTCTCTACTAAAAATACAG AGCTTGGCGACTGAGCAAGACTCCCTCTCAAA_____CAAAAAAAAGTCTCTACTAAAAATACAG GTTTGT G H2AZ2 Ensembl:ENSG00000105968 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1345663914 Functional Loss DEL dbSNP153 33..37 33 - - - Human_RBP_ID_8147530,Human_RBP_ID_18101069 RMVar_hsa_circ_116558,RMVar_hsa_circ_245017 38780 RMVar_ID_38780 Human_SNP_ID_318897670 A-to-I Human chr7 - 44833263 44833263 44833263 GCGCCACTGCACTCCAGCTTGGCGACTGAGCAAGACTCCCTCTCAAAACAAACAAAAAAAAGTCT GCGCCACTGCACTCCAGCTTGGCGACTGAGCAGGACTCCCTCTCAAAACAAACAAAAAAAAGTCT T C H2AZ2 Ensembl:ENSG00000105968 Protein coding intron GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs1377367113 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8147530 RMVar_hsa_circ_116558,RMVar_hsa_circ_245017 38781 RMVar_ID_38781 Human_SNP_ID_318897681 A-to-I Human chr7 - 44833280 44833280 44833280 TGCAGTGAGCCAAGATGGCGCCACTGCACTCCAGCTTGGCGACTGAGCAAGACTCCCTCTCAAAA TGCAGTGAGCCAAGATGGCGCCACTGCACTCCGGCTTGGCGACTGAGCAAGACTCCCTCTCAAAA T C H2AZ2 Ensembl:ENSG00000105968 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1157157393 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_685050,Human_RBP_ID_26105767 RMVar_hsa_circ_116558,RMVar_hsa_circ_245017 38782 RMVar_ID_38782 Human_SNP_ID_318897683 A-to-I Human chr7 - 44833290 44833290 44833290 AGGCGGAGCTTGCAGTGAGCCAAGATGGCGCCACTGCACTCCAGCTTGGCGACTGAGCAAGACTC AGGCGGAGCTTGCAGTGAGCCAAGATGGCGCCGCTGCACTCCAGCTTGGCGACTGAGCAAGACTC T C H2AZ2 Ensembl:ENSG00000105968 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs370336288 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_685050,Human_RBP_ID_26105768 RMVar_hsa_circ_116558,RMVar_hsa_circ_245017 38783 RMVar_ID_38783 Human_SNP_ID_318897754 A-to-I Human chr7 - 44833453 44833453 44833453 AGGTGGGTGAATCACGAGGTCAGGAAATCGAGACCATCCTGGCTAACATGGTGAAACCCCGTCTC AGGTGGGTGAATCACGAGGTCAGGAAATCGAGGCCATCCTGGCTAACATGGTGAAACCCCGTCTC T C H2AZ2 Ensembl:ENSG00000105968 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs958291513 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116558,RMVar_hsa_circ_245017 38784 RMVar_ID_38784 Human_SNP_ID_318897794 A-to-I Human chr7 - 44833590 44833590 44833590 TCCCAACACTTCGGGAGACCGAGGCTGGTGGAACACTTGAGGTCAGGAGTTTGAGACCAGCCTGG TCCCAACACTTCGGGAGACCGAGGCTGGTGGAGCACTTGAGGTCAGGAGTTTGAGACCAGCCTGG T C H2AZ2 Ensembl:ENSG00000105968 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,frontal_cortex - 29129909,30559470 RNA-Seq:(High) rs1177025400 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7742574,Human_RBP_ID_8218834,Human_RBP_ID_8668032,Human_RBP_ID_16166254,Human_RBP_ID_23197881,Human_RBP_ID_26550503 RMVar_hsa_circ_116558,RMVar_hsa_circ_245017 38785 RMVar_ID_38785 Human_SNP_ID_318897801 A-to-I Human chr7 - 44833615 44833615 44833615 CTGGCATTGTGGTTTACGCCTGTAATCCCAACACTTCGGGAGACCGAGGCTGGTGGAACACTTGA CTGGCATTGTGGTTTACGCCTGTAATCCCAACGCTTCGGGAGACCGAGGCTGGTGGAACACTTGA T C H2AZ2 Ensembl:ENSG00000105968 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1209873321 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_685051,Human_RBP_ID_4963677,Human_RBP_ID_7742574,Human_RBP_ID_8218834,Human_RBP_ID_16166254,Human_RBP_ID_23197881,Human_RBP_ID_23315754,Human_RBP_ID_26547157 RMVar_hsa_circ_116558,RMVar_hsa_circ_245017 38786 RMVar_ID_38786 Human_SNP_ID_318899106 A-to-I Human chr7 - 44838468 44838468 44838468 TTGTTATTTTCTTGTAGAGACAAGGTTTTGCCATGTTGGCCAGGCTGATCTCGAACTCCTGACCT TTGTTATTTTCTTGTAGAGACAAGGTTTTGCCGTGTTGGCCAGGCTGATCTCGAACTCCTGACCT T C H2AZ2 Ensembl:ENSG00000105968 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1336406021 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116558,RMVar_hsa_circ_245017,RMVar_hsa_circ_292601 38787 RMVar_ID_38787 Human_SNP_ID_318899134 A-to-I Human chr7 - 44838590 44838590 44838590 GGAAGGCAGGGACATGATCTCTGCTCATTGCAACCTCTGCCTTCTGGGTTCCAGTAATTCTCCCA GGAAGGCAGGGACATGATCTCTGCTCATTGCAGCCTCTGCCTTCTGGGTTCCAGTAATTCTCCCA T C H2AZ2 Ensembl:ENSG00000105968 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1158509591 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116558,RMVar_hsa_circ_245017,RMVar_hsa_circ_292601 38788 RMVar_ID_38788 Human_SNP_ID_318899680 A-to-I Human chr7 - 44840725 44840725 44840725 ACTCTTGTTTCCCAGGCTGGAGTGCAATGGCCAGTCTCGGCTCACTGCAACCTCTGCCTCCCGGA ACTCTTGTTTCCCAGGCTGGAGTGCAATGGCCGGTCTCGGCTCACTGCAACCTCTGCCTCCCGGA T C H2AZ2 Ensembl:ENSG00000105968 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388233335 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116558,RMVar_hsa_circ_245017,RMVar_hsa_circ_292601 38789 RMVar_ID_38789 Human_SNP_ID_318900229 A-to-I Human chr7 - 44843092 44843092 44843092 ACTCTGTCGTCAGGCTGGAGTGCAGTGGTGCAATCTCGGCTCACTGCAACCTCTGCCTCCTGGAT ACTCTGTCGTCAGGCTGGAGTGCAGTGGTGCAGTCTCGGCTCACTGCAACCTCTGCCTCCTGGAT T C H2AZ2 Ensembl:ENSG00000105968 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749062057 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116558,RMVar_hsa_circ_93740,RMVar_hsa_circ_245017,RMVar_hsa_circ_272839,RMVar_hsa_circ_292601,RMVar_hsa_circ_245019,RMVar_hsa_circ_245020 38790 RMVar_ID_38790 Human_SNP_ID_318909401 A-to-I Human chr7 - 44877637 44877637 44877637 ACCATGCCCAGCTAATTTTCTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGG ACCATGCCCAGCTAATTTTCTGTATTTTTAGTGGAGACGGGGTTTCACCATGTTGGCCAGGCTGG T C PURB Ensembl:ENSG00000146676 Protein coding 3'UTR GSE47997;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;Bronchiolar epithelium,BERP35T1 cell line - 23474544,31158229 RNA-Seq:(High) rs984526340 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_176100 38791 RMVar_ID_38791 Human_SNP_ID_318909412 A-to-I Human chr7 - 44877679 44877679 44877679 CTGCCTCAGCCTCCCAAGTAGCTGGGATTACAAGCATGTGCCACCATGCCCAGCTAATTTTCTGT CTGCCTCAGCCTCCCAAGTAGCTGGGATTACATGCATGTGCCACCATGCCCAGCTAATTTTCTGT T A PURB Ensembl:ENSG00000146676 Protein coding 3'UTR GSE47997;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;Bronchiolar epithelium,BERP35T1 cell line - 23474544,31158229 RNA-Seq:(High) rs1248901607 Functional Loss SNV dbSNP153 33..33 33 - - - 38792 RMVar_ID_38792 Human_SNP_ID_318909806 A-to-I Human chr7 - 44879300 44879300 44879300 AAATGCGGCCGGGCGTGGTGGCTCACGCCTGTAATCCCAGCACTCTGGGAGGCTGAGGTGGGCGG AAATGCGGCCGGGCGTGGTGGCTCACGCCTGTCATCCCAGCACTCTGGGAGGCTGAGGTGGGCGG T G PURB Ensembl:ENSG00000146676 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs555617665 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8218843 38793 RMVar_ID_38793 Human_SNP_ID_318915063 A-to-I Human chr7 + 44899065 44899065 44899065 GTGATCCTCCAGCCTCAGCCTTCCAAAGTGTTAGGATTATAGGCATGAGCCACCATGCCCAGCCA GTGATCCTCCAGCCTCAGCCTTCCAAAGTGTTCGGATTATAGGCATGAGCCACCATGCCCAGCCA A C lnc-PPIA-1 RNACentral:URS0000D5A2B4 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1458574184 Functional Loss SNV dbSNP153 33..33 33 - - - 38794 RMVar_ID_38794 Human_SNP_ID_520858653 A-to-I Human chr12 - 130791398 130791398 130791398 CCTCAGCCTCCCGAGTAGCTGGGATTACAGGCATGGGCCACCACACCCAGCTAATTTTTTGTGTT CCTCAGCCTCCCGAGTAGCTGGGATTACAGGCGTGGGCCACCACACCCAGCTAATTTTTTGTGTT T C STX2 Ensembl:ENSG00000111450 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1356644842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3398038 38795 RMVar_ID_38795 Human_SNP_ID_520861472 A-to-I Human chr12 - 130802309 130802309 130802309 CGTGTAGTCCCCACCACTCAGGGGTCAGAGGCATGAGAATTGCTTGAACCCGGGAGGAAGAGGTT CGTGTAGTCCCCACCACTCAGGGGTCAGAGGCGTGAGAATTGCTTGAACCCGGGAGGAAGAGGTT T C STX2 Ensembl:ENSG00000111450 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs546304813 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11875380 RMVar_hsa_circ_161695,RMVar_hsa_circ_86506,RMVar_hsa_circ_349683,RMVar_hsa_circ_314158,RMVar_hsa_circ_302046,RMVar_hsa_circ_53796,RMVar_hsa_circ_161697,RMVar_hsa_circ_161696,RMVar_hsa_circ_326062,RMVar_hsa_circ_368824,RMVar_hsa_circ_294702,RMVar_hsa_circ_46738,RMVar_hsa_circ_319686,RMVar_hsa_circ_161703,RMVar_hsa_circ_161704 38796 RMVar_ID_38796 Human_SNP_ID_520861505 A-to-I Human chr12 - 130802377 130802377 130802377 CCTGGCCAAAATGGTGAAACCCCACCTCTACTAAAAATACAAAAATTAGCCGGGCGTGGTGACGC CCTGGCCAAAATGGTGAAACCCCACCTCTACTGAAAATACAAAAATTAGCCGGGCGTGGTGACGC T C STX2 Ensembl:ENSG00000111450 Protein coding intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1331253783 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_161695,RMVar_hsa_circ_86506,RMVar_hsa_circ_349683,RMVar_hsa_circ_314158,RMVar_hsa_circ_302046,RMVar_hsa_circ_53796,RMVar_hsa_circ_161697,RMVar_hsa_circ_161696,RMVar_hsa_circ_326062,RMVar_hsa_circ_368824,RMVar_hsa_circ_294702,RMVar_hsa_circ_46738,RMVar_hsa_circ_319686,RMVar_hsa_circ_161703,RMVar_hsa_circ_161704 38797 RMVar_ID_38797 Human_SNP_ID_520861545 A-to-I Human chr12 - 130802552 130802552 130802552 TCAAAGCGGCAGTGAGCTGAGATTGCACCACTACACTCCAGTCTGGGTGACAGAGTGAGACCGTA TCAAAGCGGCAGTGAGCTGAGATTGCACCACTGCACTCCAGTCTGGGTGACAGAGTGAGACCGTA T C STX2 Ensembl:ENSG00000111450 Protein coding intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1158429112 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_161695,RMVar_hsa_circ_86506,RMVar_hsa_circ_349683,RMVar_hsa_circ_314158,RMVar_hsa_circ_302046,RMVar_hsa_circ_53796,RMVar_hsa_circ_161697,RMVar_hsa_circ_161696,RMVar_hsa_circ_326062,RMVar_hsa_circ_368824,RMVar_hsa_circ_294702,RMVar_hsa_circ_46738,RMVar_hsa_circ_319686,RMVar_hsa_circ_161703,RMVar_hsa_circ_161704 38798 RMVar_ID_38798 Human_SNP_ID_520861558 A-to-I Human chr12 - 130802609 130802609 130802609 CCTATAATCACAGTCACTTGGGAGGCTGGAGCAGGAGGATTGCTTGAGCCTAGGAGGTCAAAGCG CCTATAATCACAGTCACTTGGGAGGCTGGAGCCGGAGGATTGCTTGAGCCTAGGAGGTCAAAGCG T G STX2 Ensembl:ENSG00000111450 Protein coding intron GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,31158229,32596459 RNA-Seq:(High) rs1462413137 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_161695,RMVar_hsa_circ_86506,RMVar_hsa_circ_349683,RMVar_hsa_circ_314158,RMVar_hsa_circ_302046,RMVar_hsa_circ_53796,RMVar_hsa_circ_161697,RMVar_hsa_circ_161696,RMVar_hsa_circ_326062,RMVar_hsa_circ_368824,RMVar_hsa_circ_294702,RMVar_hsa_circ_46738,RMVar_hsa_circ_319686,RMVar_hsa_circ_161703,RMVar_hsa_circ_161704 38799 RMVar_ID_38799 Human_SNP_ID_520861709 A-to-I Human chr12 - 130803349 130803349 130803349 ATTGAGCTATTTTGAATAGATTTTTAAGTTTTATTTTATTTTTTGTAGAGATAGGGTCTTGCTGT ATTGAGCTATTTTGAATAGATTTTTAAGTTTTGTTTTATTTTTTGTAGAGATAGGGTCTTGCTGT T C STX2 Ensembl:ENSG00000111450 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1423102576 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6152270 RMVar_hsa_circ_161695,RMVar_hsa_circ_86506,RMVar_hsa_circ_349683,RMVar_hsa_circ_314158,RMVar_hsa_circ_302046,RMVar_hsa_circ_53796,RMVar_hsa_circ_161697,RMVar_hsa_circ_161696,RMVar_hsa_circ_326062,RMVar_hsa_circ_368824,RMVar_hsa_circ_294702,RMVar_hsa_circ_46738,RMVar_hsa_circ_319686,RMVar_hsa_circ_161703,RMVar_hsa_circ_161704 38800 RMVar_ID_38800 Human_SNP_ID_520861738 A-to-I Human chr12 - 130803504 130803504 130803504 CACCACCATACCTGGCTAATTTTATTTTTTGTAGAGACGAGGTTTTCACTATGTTGCCCAAGCTG CACCACCATACCTGGCTAATTTTATTTTTTGTTGAGACGAGGTTTTCACTATGTTGCCCAAGCTG T A STX2 Ensembl:ENSG00000111450 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1005231454 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11875385,Human_RBP_ID_23547503 RMVar_hsa_circ_161695,RMVar_hsa_circ_86506,RMVar_hsa_circ_349683,RMVar_hsa_circ_314158,RMVar_hsa_circ_302046,RMVar_hsa_circ_53796,RMVar_hsa_circ_161697,RMVar_hsa_circ_161696,RMVar_hsa_circ_326062,RMVar_hsa_circ_368824,RMVar_hsa_circ_294702,RMVar_hsa_circ_46738,RMVar_hsa_circ_319686,RMVar_hsa_circ_161703,RMVar_hsa_circ_161704 38801 RMVar_ID_38801 Human_SNP_ID_520861739 A-to-I Human chr12 - 130803504 130803504 130803504 CACCACCATACCTGGCTAATTTTATTTTTTGTAGAGACGAGGTTTTCACTATGTTGCCCAAGCTG CACCACCATACCTGGCTAATTTTATTTTTTGTGGAGACGAGGTTTTCACTATGTTGCCCAAGCTG T C STX2 Ensembl:ENSG00000111450 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1005231454 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11875385,Human_RBP_ID_23547503 RMVar_hsa_circ_161695,RMVar_hsa_circ_86506,RMVar_hsa_circ_349683,RMVar_hsa_circ_314158,RMVar_hsa_circ_302046,RMVar_hsa_circ_53796,RMVar_hsa_circ_161697,RMVar_hsa_circ_161696,RMVar_hsa_circ_326062,RMVar_hsa_circ_368824,RMVar_hsa_circ_294702,RMVar_hsa_circ_46738,RMVar_hsa_circ_319686,RMVar_hsa_circ_161703,RMVar_hsa_circ_161704 38802 RMVar_ID_38802 Human_SNP_ID_520861753 A-to-I Human chr12 - 130803545 130803545 130803545 CTCCCACCTCAGCCTCTCGAGTAGCTGGGACCACAGAAGCACACCACCATACCTGGCTAATTTTA CTCCCACCTCAGCCTCTCGAGTAGCTGGGACCGCAGAAGCACACCACCATACCTGGCTAATTTTA T C STX2 Ensembl:ENSG00000111450 Protein coding intron GSE38233;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,32596459 RNA-Seq:(High) rs1400744682 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_161695,RMVar_hsa_circ_86506,RMVar_hsa_circ_349683,RMVar_hsa_circ_314158,RMVar_hsa_circ_302046,RMVar_hsa_circ_53796,RMVar_hsa_circ_161697,RMVar_hsa_circ_161696,RMVar_hsa_circ_326062,RMVar_hsa_circ_368824,RMVar_hsa_circ_294702,RMVar_hsa_circ_46738,RMVar_hsa_circ_319686,RMVar_hsa_circ_161703,RMVar_hsa_circ_161704 38803 RMVar_ID_38803 Human_SNP_ID_520861864 A-to-I Human chr12 - 130803747 130803747 130803747 TCTGTAACCCCAGGCTGTTTCTTAGACTTAGCAGTTAGCCGGTGGGAAGACCTTTGTGAACGTGA TCTGTAACCCCAGGCTGTTTCTTAGACTTAGCGGTTAGCCGGTGGGAAGACCTTTGTGAACGTGA T C STX2 Ensembl:ENSG00000111450 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2037789 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_4385,GWAS_ID_4386,GWAS_ID_4387 RMVar_hsa_circ_161695,RMVar_hsa_circ_86506,RMVar_hsa_circ_349683,RMVar_hsa_circ_314158,RMVar_hsa_circ_302046,RMVar_hsa_circ_53796,RMVar_hsa_circ_161697,RMVar_hsa_circ_161696,RMVar_hsa_circ_326062,RMVar_hsa_circ_368824,RMVar_hsa_circ_294702,RMVar_hsa_circ_46738,RMVar_hsa_circ_319686,RMVar_hsa_circ_161703,RMVar_hsa_circ_161704 38804 RMVar_ID_38804 Human_SNP_ID_521124412 A-to-I Human chr12 + 131773544 131773544 131773544 TTTTGTATTTTTGGTAGAGATGGGATTTTGCTATATTGCCCAGACTGGTCTTGAACTCCTGGCCT TTTTGTATTTTTGGTAGAGATGGGATTTTGCTGTATTGCCCAGACTGGTCTTGAACTCCTGGCCT A G SFSWAP Ensembl:ENSG00000061936 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1271300384 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51181,RMVar_hsa_circ_50163,RMVar_hsa_circ_52589,RMVar_hsa_circ_33101,RMVar_hsa_circ_161739,RMVar_hsa_circ_375465,RMVar_hsa_circ_161740,RMVar_hsa_circ_318889,RMVar_hsa_circ_360958,RMVar_hsa_circ_322754,RMVar_hsa_circ_161741 38805 RMVar_ID_38805 Human_SNP_ID_521127021 A-to-I Human chr12 + 131783130 131783130 131783130 TTGAACCCGGGAGGTGGAGATTGCAGTGAGCCAAGATCGTGTCACTGCTCTCCAGCCTGGGCAAT TTGAACCCGGGAGGTGGAGATTGCAGTGAGCCCAGATCGTGTCACTGCTCTCCAGCCTGGGCAAT A C SFSWAP Ensembl:ENSG00000061936 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs143731652 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50163,RMVar_hsa_circ_33101,RMVar_hsa_circ_161739,RMVar_hsa_circ_375465,RMVar_hsa_circ_360958,RMVar_hsa_circ_352864 38806 RMVar_ID_38806 Human_SNP_ID_521129868 A-to-I Human chr12 + 131793273 131793273 131793273 CCAGCTAATTTTTTTTTATTGTGTGTAGAGACAGGGTCTCGCTATGTTGCCCAGGCTGATGTTGA CCAGCTAATTTTTTTTTATTGTGTGTAGAGACGGGGTCTCGCTATGTTGCCCAGGCTGATGTTGA A G SFSWAP Ensembl:ENSG00000061936 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886791345 Functional Loss SNV dbSNP153 33..33 33 - - - 38807 RMVar_ID_38807 Human_SNP_ID_521129872 A-to-I Human chr12 + 131793284 131793284 131793284 TTTTTTATTGTGTGTAGAGACAGGGTCTCGCTATGTTGCCCAGGCTGATGTTGAACTCCCAGGCT TTTTTTATTGTGTGTAGAGACAGGGTCTCGCTCTGTTGCCCAGGCTGATGTTGAACTCCCAGGCT A C SFSWAP Ensembl:ENSG00000061936 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1286898353 Functional Loss SNV dbSNP153 33..33 33 - - - 38808 RMVar_ID_38808 Human_SNP_ID_521145672 A-to-I Human chr12 + 131846078 131846078 131846078 CCAAGTCTCCGGGAAGGGCAGGAAAGGGAGACAGTAGCAGGGGCAGGTGGGGGTGGCAGGGCTGC CCAAGTCTCCGGGAAGGGCAGGAAAGGGAGACGGTAGCAGGGGCAGGTGGGGGTGGCAGGGCTGC A G MMP17 Ensembl:ENSG00000198598 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1428153029 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18514,RMVar_hsa_circ_269247 38809 RMVar_ID_38809 Human_SNP_ID_521145767 A-to-I Human chr12 + 131846432 131846432 131846432 AAAGTCTCACTCTGTTGCCCAGGCTGGAATGCAATGGTGTGATCTCAGCTCACTGCAACCTTCAC AAAGTCTCACTCTGTTGCCCAGGCTGGAATGCCATGGTGTGATCTCAGCTCACTGCAACCTTCAC A C MMP17 Ensembl:ENSG00000198598 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1456252328 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18514,RMVar_hsa_circ_269247 38810 RMVar_ID_38810 Human_SNP_ID_521175022 A-to-I Human chr12 + 131936151 131936151 131936151 GAGAATTGCGTGAACCTGGGAGGCGGAGGTTGAAGTAAGCTGAGATGGTGCCACTGCACTGCAGC GAGAATTGCGTGAACCTGGGAGGCGGAGGTTGGAGTAAGCTGAGATGGTGCCACTGCACTGCAGC A G PUS1 Ensembl:ENSG00000177192 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1330599195 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11878301,Human_RBP_ID_23156970 RMVar_hsa_circ_15521,RMVar_hsa_circ_110077,RMVar_hsa_circ_51260,RMVar_hsa_circ_114954,RMVar_hsa_circ_161750,RMVar_hsa_circ_161751 38811 RMVar_ID_38811 Human_SNP_ID_521175144 A-to-I Human chr12 + 131936456 131936456 131936456 GTGGTGGTGCACGCCTGTAATCCCAGCTACTCAGTAGGCTGAGGCAGGAGAATCGTTTGAATCCG GTGGTGGTGCACGCCTGTAATCCCAGCTACTCGGTAGGCTGAGGCAGGAGAATCGTTTGAATCCG A G PUS1 Ensembl:ENSG00000177192 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs954251094 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11878307,Human_RBP_ID_24949256 RMVar_hsa_circ_15521,RMVar_hsa_circ_110077,RMVar_hsa_circ_51260,RMVar_hsa_circ_114954,RMVar_hsa_circ_161750,RMVar_hsa_circ_161751 38812 RMVar_ID_38812 Human_SNP_ID_521175208 A-to-I Human chr12 + 131936633 131936633 131936633 GGTTCAAGCTGGGTGTGGTGGCTCACGCCTGTAATCCCAACACTTTGGGAGGCCAAAGTGGACGG GGTTCAAGCTGGGTGTGGTGGCTCACGCCTGTTATCCCAACACTTTGGGAGGCCAAAGTGGACGG A T PUS1 Ensembl:ENSG00000177192 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs888399469 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11878311 RMVar_hsa_circ_15521,RMVar_hsa_circ_110077,RMVar_hsa_circ_51260,RMVar_hsa_circ_114954,RMVar_hsa_circ_161750,RMVar_hsa_circ_161751 38813 RMVar_ID_38813 Human_SNP_ID_521175221 A-to-I Human chr12 + 131936669 131936669 131936669 CCAACACTTTGGGAGGCCAAAGTGGACGGATCACTTGAGGCCAGGAGTTCGAGACCAGCCTGGCC CCAACACTTTGGGAGGCCAAAGTGGACGGATCGCTTGAGGCCAGGAGTTCGAGACCAGCCTGGCC A G PUS1 Ensembl:ENSG00000177192 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1417557886 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15521,RMVar_hsa_circ_110077,RMVar_hsa_circ_51260,RMVar_hsa_circ_114954,RMVar_hsa_circ_161750,RMVar_hsa_circ_161751 38814 RMVar_ID_38814 Human_SNP_ID_521175244 A-to-I Human chr12 + 131936778 131936778 131936778 AGGCATGGTGGCTTACACCTGTAATCCCAGCTACCTGGGAGGCTGAGGCAGGAGAATCTCTTGAA AGGCATGGTGGCTTACACCTGTAATCCCAGCTTCCTGGGAGGCTGAGGCAGGAGAATCTCTTGAA A T PUS1 Ensembl:ENSG00000177192 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1344861226 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15521,RMVar_hsa_circ_110077,RMVar_hsa_circ_51260,RMVar_hsa_circ_114954,RMVar_hsa_circ_161750,RMVar_hsa_circ_161751 38815 RMVar_ID_38815 Human_SNP_ID_521175473 A-to-I Human chr12 + 131937650 131937650 131937650 CGCCTGCCCCGGCTTCCCAAAGTGCTGGGATTACAGGCATGAACCACCGCACTCCGCCCGTTTTT CGCCTGCCCCGGCTTCCCAAAGTGCTGGGATTGCAGGCATGAACCACCGCACTCCGCCCGTTTTT A G PUS1 Ensembl:ENSG00000177192 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1173905522 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6153606,Human_RBP_ID_11878362 RMVar_hsa_circ_15521,RMVar_hsa_circ_110077,RMVar_hsa_circ_51260,RMVar_hsa_circ_114954,RMVar_hsa_circ_161750,RMVar_hsa_circ_161751 38816 RMVar_ID_38816 Human_SNP_ID_521175474 A-to-I Human chr12 + 131937656 131937656 131937656 CCCCGGCTTCCCAAAGTGCTGGGATTACAGGCATGAACCACCGCACTCCGCCCGTTTTTTTGTTT CCCCGGCTTCCCAAAGTGCTGGGATTACAGGCGTGAACCACCGCACTCCGCCCGTTTTTTTGTTT A G PUS1 Ensembl:ENSG00000177192 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1422469853 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6153606,Human_RBP_ID_11878362 RMVar_hsa_circ_15521,RMVar_hsa_circ_110077,RMVar_hsa_circ_51260,RMVar_hsa_circ_114954,RMVar_hsa_circ_161750,RMVar_hsa_circ_161751 38817 RMVar_ID_38817 Human_SNP_ID_521175509 A-to-I Human chr12 + 131937735 131937734 131937736 TTTATTTATCTTTTTTTTACCTTTTTTGAGACAGAGTCTTGCTCTGTTGCCCAGGCTGGTCTTGA TTTATTTATCTTTTTTTTACCTTTTTTGAGAC__AGTCTTGCTCTGTTGCCCAGGCTGGTCTTGA CAG C PUS1 Ensembl:ENSG00000177192 Protein coding intron GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line - 24183664,31158229 RNA-Seq:(High) rs573173172 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_2313802,Human_RBP_ID_6153609,Human_RBP_ID_9712256,Human_RBP_ID_12077500,Human_RBP_ID_23156980,Human_RBP_ID_25021081 RMVar_hsa_circ_15521,RMVar_hsa_circ_110077,RMVar_hsa_circ_51260,RMVar_hsa_circ_114954,RMVar_hsa_circ_161750,RMVar_hsa_circ_161751 38818 RMVar_ID_38818 Human_SNP_ID_521175626 A-to-I Human chr12 + 131938202 131938202 131938202 ATCGTTGCTTACACCTGTAATCCCAGCACTTTATGAGACTGAGGTGGGAGGATCACTTGAGGCCA ATCGTTGCTTACACCTGTAATCCCAGCACTTTGTGAGACTGAGGTGGGAGGATCACTTGAGGCCA A G PUS1 Ensembl:ENSG00000177192 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs994271862 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11878396,Human_RBP_ID_23547943,Human_RBP_ID_24949292 RMVar_hsa_circ_15521,RMVar_hsa_circ_110077,RMVar_hsa_circ_51260,RMVar_hsa_circ_114954,RMVar_hsa_circ_161750,RMVar_hsa_circ_161751 38819 RMVar_ID_38819 Human_SNP_ID_521175682 A-to-I Human chr12 + 131938389 131938389 131938389 ATTGCTCAAACCTGGGAGGTCAAGGTTGCTGTAAGCCAAGATCGGCACCACTGCACTCCAACCTG ATTGCTCAAACCTGGGAGGTCAAGGTTGCTGTTAGCCAAGATCGGCACCACTGCACTCCAACCTG A T PUS1 Ensembl:ENSG00000177192 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1009258333 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6153624,Human_RBP_ID_9671080,Human_RBP_ID_11878401,Human_RBP_ID_17561343,Human_RBP_ID_22901089,Human_RBP_ID_23305744,Human_RBP_ID_25021085 RMVar_hsa_circ_15521,RMVar_hsa_circ_110077,RMVar_hsa_circ_51260,RMVar_hsa_circ_114954,RMVar_hsa_circ_161750,RMVar_hsa_circ_161751 38820 RMVar_ID_38820 Human_SNP_ID_521175831 A-to-I Human chr12 + 131938887 131938887 131938887 GGGACTACAGGCGCCTGTCACCATGCCCGGCTAATTTTTTGTATTTTTAGTAGAGACTAACAATA GGGACTACAGGCGCCTGTCACCATGCCCGGCTCATTTTTTGTATTTTTAGTAGAGACTAACAATA A C PUS1 Ensembl:ENSG00000177192 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559237472 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11878433 RMVar_hsa_circ_15521,RMVar_hsa_circ_110077,RMVar_hsa_circ_51260,RMVar_hsa_circ_114954,RMVar_hsa_circ_161750,RMVar_hsa_circ_161751 38821 RMVar_ID_38821 Human_SNP_ID_521175853 A-to-I Human chr12 + 131938948 131938948 131938948 AATACATTTAGTAGAGACTAACATTTCATGTTAGCCAGGATAGTCTCGATCTCCTGACCTCGTGA AATACATTTAGTAGAGACTAACATTTCATGTTGGCCAGGATAGTCTCGATCTCCTGACCTCGTGA A G PUS1 Ensembl:ENSG00000177192 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs879121721 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6153639 RMVar_hsa_circ_15521,RMVar_hsa_circ_110077,RMVar_hsa_circ_51260,RMVar_hsa_circ_114954,RMVar_hsa_circ_161750,RMVar_hsa_circ_161751 38822 RMVar_ID_38822 Human_SNP_ID_521175881 A-to-I Human chr12 + 131939006 131939006 131939006 CTCGTGATCCACCCGCCTCGGCCTCCCAAAGTACTGGGATTACAGGCGTGAGCCACTATGCCCGG CTCGTGATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTATGCCCGG A G PUS1 Ensembl:ENSG00000177192 Protein coding intron GSE38233;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;Bronchiolar epithelium,BERP35T4 cell line - 24183664,31158229 RNA-Seq:(High) rs1016497655 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15521,RMVar_hsa_circ_110077,RMVar_hsa_circ_51260,RMVar_hsa_circ_114954,RMVar_hsa_circ_161750,RMVar_hsa_circ_161751 38823 RMVar_ID_38823 Human_SNP_ID_521187356 A-to-I Human chr12 + 131978344 131978344 131978344 TGGTGAAACCTTCAGTGCCATGTCATTAGCATAGTACTGTAGTTTCACCGCCCTAGAAATGTCCC TGGTGAAACCTTCAGTGCCATGTCATTAGCATCGTACTGTAGTTTCACCGCCCTAGAAATGTCCC A C EP400 Ensembl:ENSG00000183495 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041062798 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11878849 RMVar_hsa_circ_266685 38824 RMVar_ID_38824 Human_SNP_ID_521187357 A-to-I Human chr12 + 131978344 131978344 131978344 TGGTGAAACCTTCAGTGCCATGTCATTAGCATAGTACTGTAGTTTCACCGCCCTAGAAATGTCCC TGGTGAAACCTTCAGTGCCATGTCATTAGCATGGTACTGTAGTTTCACCGCCCTAGAAATGTCCC A G EP400 Ensembl:ENSG00000183495 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041062798 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11878849 RMVar_hsa_circ_266685 38825 RMVar_ID_38825 Human_SNP_ID_521187458 A-to-I Human chr12 + 131978702 131978702 131978702 TAACATTTTAATTTTTATTTTTTTGTAGAGACAGGATCTTGCTGTGTTGCCCAGGCTGGTTTTGA TAACATTTTAATTTTTATTTTTTTGTAGAGACTGGATCTTGCTGTGTTGCCCAGGCTGGTTTTGA A T EP400 Ensembl:ENSG00000183495 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232494330 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266685 38826 RMVar_ID_38826 Human_SNP_ID_521189270 A-to-I Human chr12 + 131985039 131985039 131985039 AGGCAACTGTTTTTTTTTTTTTACTTTTTAGTAGAGATGGGCTTTTGCCATGTTGGCCAGGCTGG AGGCAACTGTTTTTTTTTTTTTACTTTTTAGTGGAGATGGGCTTTTGCCATGTTGGCCAGGCTGG A G EP400 Ensembl:ENSG00000183495 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs529565558 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6106,RMVar_hsa_circ_266685,RMVar_hsa_circ_96255,RMVar_hsa_circ_267017,RMVar_hsa_circ_347175,RMVar_hsa_circ_27900,RMVar_hsa_circ_362687,RMVar_hsa_circ_161755,RMVar_hsa_circ_318788,RMVar_hsa_circ_113158,RMVar_hsa_circ_161756 38827 RMVar_ID_38827 Human_SNP_ID_521193070 A-to-I Human chr12 + 131998903 131998889 131998903 ATACAAAGACTTTGTATACAGTCTTGTATACAAAGTCTTTGTATACAGTCTTGTATACAAAGTCT ATACAAAGACTTTGTATAC______________AGTCTTTGTATACAGTCTTGTATACAAAGTCT CAGTCTTGTATACAA C EP400 Ensembl:ENSG00000183495 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1220252107 Functional Loss DEL dbSNP153 20..33 33 - - - RMVar_hsa_circ_6106,RMVar_hsa_circ_266685,RMVar_hsa_circ_96255,RMVar_hsa_circ_267017,RMVar_hsa_circ_82298,RMVar_hsa_circ_27986,RMVar_hsa_circ_27900,RMVar_hsa_circ_161755,RMVar_hsa_circ_113158,RMVar_hsa_circ_322518,RMVar_hsa_circ_161756,RMVar_hsa_circ_161758,RMVar_hsa_circ_161759,RMVar_hsa_circ_123706,RMVar_hsa_circ_6053,RMVar_hsa_circ_302937,RMVar_hsa_circ_161760,RMVar_hsa_circ_284352,RMVar_hsa_circ_115942,RMVar_hsa_circ_161761,RMVar_hsa_circ_161762 38828 RMVar_ID_38828 Human_SNP_ID_521193080 A-to-I Human chr12 + 131998903 131998903 131998903 ATACAAAGACTTTGTATACAGTCTTGTATACAAAGTCTTTGTATACAGTCTTGTATACAAAGTCT ATACAAAGACTTTGTATACAGTCTTGTATACAGAGTCTTTGTATACAGTCTTGTATACAAAGTCT A G EP400 Ensembl:ENSG00000183495 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1476635761 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6106,RMVar_hsa_circ_266685,RMVar_hsa_circ_96255,RMVar_hsa_circ_267017,RMVar_hsa_circ_82298,RMVar_hsa_circ_27986,RMVar_hsa_circ_27900,RMVar_hsa_circ_161755,RMVar_hsa_circ_113158,RMVar_hsa_circ_322518,RMVar_hsa_circ_161756,RMVar_hsa_circ_161758,RMVar_hsa_circ_161759,RMVar_hsa_circ_123706,RMVar_hsa_circ_6053,RMVar_hsa_circ_302937,RMVar_hsa_circ_161760,RMVar_hsa_circ_284352,RMVar_hsa_circ_115942,RMVar_hsa_circ_161761,RMVar_hsa_circ_161762 38829 RMVar_ID_38829 Human_SNP_ID_521224368 A-to-I Human chr12 + 132110496 132110496 132110496 GAAACCCCATCTCTACTAAAAATGCAAAGATTAGCCGGGCTTGGTGGCGGGCACCTGTAATCCCA GAAACCCCATCTCTACTAAAAATGCAAAGATTGGCCGGGCTTGGTGGCGGGCACCTGTAATCCCA A G EP400P1 Ensembl:ENSG00000185684 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs765648786 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11880919 RMVar_hsa_circ_68717,RMVar_hsa_circ_304259,RMVar_hsa_circ_161777,RMVar_hsa_circ_96098,RMVar_hsa_circ_161778 38830 RMVar_ID_38830 Human_SNP_ID_521411852 A-to-I Human chr12 - 132652450 132652450 132652450 AGGCATGGTTGTGCATGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGTGGGAGGATCACTTGAG AGGCATGGTTGTGCATGCCTGTAGTCCCAGCTGCTTGGGAGGCTGAGGTGGGAGGATCACTTGAG T C POLE Ensembl:ENSG00000177084 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1402979443 Functional Loss SNV dbSNP153 33..33 33 - - - 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 38831 RMVar_ID_38831 Human_SNP_ID_521412497 A-to-I Human chr12 - 132654995 132654995 132654995 AAGGCTGAGAGGCAGGAGGATTGCTTGAGCCCAGGAATTTGAGGTTGTAGTGGGCTATGATGGCA AAGGCTGAGAGGCAGGAGGATTGCTTGAGCCCGGGAATTTGAGGTTGTAGTGGGCTATGATGGCA T C POLE Ensembl:ENSG00000177084 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910446264 Functional Loss SNV dbSNP153 33..33 33 - - - 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 38832 RMVar_ID_38832 Human_SNP_ID_521412808 A-to-I Human chr12 - 132656262 132656262 132656262 TTCCCCTGCCCCCCAAGACGGAGTCTTGCTCTATTGCCCAGGCAGGAGTGCAGTGGCACAATGCA TTCCCCTGCCCCCCAAGACGGAGTCTTGCTCTGTTGCCCAGGCAGGAGTGCAGTGGCACAATGCA T C POLE Ensembl:ENSG00000177084 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1018121805 Functional Loss SNV dbSNP153 33..33 33 - - - 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 38833 RMVar_ID_38833 Human_SNP_ID_521425917 A-to-I Human chr12 + 132696259 132696259 132696259 GAGTCACTTTATTTATTTATTTATTTAAAGACAGGGTTTCACTCTGTCACCCAGGCTGCAGTGCA GAGTCACTTTATTTATTTATTTATTTAAAGACGGGGTTTCACTCTGTCACCCAGGCTGCAGTGCA A G PXMP2,AC135586.2 Ensembl:ENSG00000176894,Ensembl:ENSG00000256632 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1253061435 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_161854,RMVar_hsa_circ_92598,RMVar_hsa_circ_357442,RMVar_hsa_circ_161855,RMVar_hsa_circ_320299 38834 RMVar_ID_38834 Human_SNP_ID_521428926 A-to-I Human chr12 + 132706567 132706567 132706567 TTGAACCTGGGAGGCAGAGGTTGCAGTGAGCCAAGATCGCTCCACTGCATTCCAGCCTGGCGACA TTGAACCTGGGAGGCAGAGGTTGCAGTGAGCCGAGATCGCTCCACTGCATTCCAGCCTGGCGACA A G AC135586.2 Ensembl:ENSG00000256632 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1396597037 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_161854,RMVar_hsa_circ_92598 38835 RMVar_ID_38835 Human_SNP_ID_521431230 A-to-I Human chr12 + 132714147 132714147 132714147 TCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATCACAGGCGTGTGCCACCAAGCCCG TCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTTGCTGGGATCACAGGCGTGTGCCACCAAGCCCG A T PGAM5,AC135586.2 Ensembl:ENSG00000247077,Ensembl:ENSG00000256632 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1395092368 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_161854,RMVar_hsa_circ_92598 38836 RMVar_ID_38836 Human_SNP_ID_521434045 A-to-I Human chr12 + 132721318 132721318 132721318 ATTTGTCAATTAAAGATTTTCTGGCTGGGCACAGTGGCTCACACCTGTATTCCCAGCTACTCAGG ATTTGTCAATTAAAGATTTTCTGGCTGGGCACCGTGGCTCACACCTGTATTCCCAGCTACTCAGG A C PGAM5 Ensembl:ENSG00000247077 Protein coding 3'UTR GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,29796672,31158229,32596459,32596459 RNA-Seq:(High) rs1009367502 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_415473,Human_RBP_ID_6154905,Human_RBP_ID_8178373,Human_RBP_ID_8247599,Human_RBP_ID_11883403,Human_RBP_ID_18257604,Human_RBP_ID_26414311,Human_RBP_ID_27420550 Human_miRNA_ID_2890614 RMVar_hsa_circ_161854,RMVar_hsa_circ_92598 38837 RMVar_ID_38837 Human_SNP_ID_521434051 A-to-I Human chr12 + 132721348 132721348 132721348 ACAGTGGCTCACACCTGTATTCCCAGCTACTCAGGAGGCCAGGGTGGGAGGATCACTTGAGCTCA ACAGTGGCTCACACCTGTATTCCCAGCTACTCGGGAGGCCAGGGTGGGAGGATCACTTGAGCTCA A G PGAM5 Ensembl:ENSG00000247077 Protein coding 3'UTR GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs1449393562 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_415473,Human_RBP_ID_4252981,Human_RBP_ID_8178373,Human_RBP_ID_8247600,Human_RBP_ID_22573976,Human_RBP_ID_23305751,Human_RBP_ID_26414311,Human_RBP_ID_27420550 Human_miRNA_ID_2868277 RMVar_hsa_circ_161854,RMVar_hsa_circ_92598 38838 RMVar_ID_38838 Human_SNP_ID_521434060 A-to-I Human chr12 + 132721380 132721380 132721380 AGGAGGCCAGGGTGGGAGGATCACTTGAGCTCAGGAGTTCAAGACCAGCCTGGACAAGGCAACAT AGGAGGCCAGGGTGGGAGGATCACTTGAGCTCCGGAGTTCAAGACCAGCCTGGACAAGGCAACAT A C PGAM5 Ensembl:ENSG00000247077 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-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 38839 RMVar_ID_38839 Human_SNP_ID_521434061 A-to-I Human chr12 + 132721380 132721380 132721380 AGGAGGCCAGGGTGGGAGGATCACTTGAGCTCAGGAGTTCAAGACCAGCCTGGACAAGGCAACAT AGGAGGCCAGGGTGGGAGGATCACTTGAGCTCGGGAGTTCAAGACCAGCCTGGACAAGGCAACAT A G PGAM5 Ensembl:ENSG00000247077 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-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 38840 RMVar_ID_38840 Human_SNP_ID_521434074 A-to-I Human chr12 + 132721433 132721433 132721433 ACAAGGCAACATAGCGAGACCCTGTCTCTACTAAAAATACAGAACTTAGCTGGGTGTGTCGTGGG ACAAGGCAACATAGCGAGACCCTGTCTCTACTGAAAATACAGAACTTAGCTGGGTGTGTCGTGGG A G PGAM5 Ensembl:ENSG00000247077 Protein coding 3'UTR GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs1262385323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_415474,Human_RBP_ID_17353123,Human_RBP_ID_27420551 RMVar_hsa_circ_161854,RMVar_hsa_circ_92598 38841 RMVar_ID_38841 Human_SNP_ID_521434083 A-to-I Human chr12 + 132721467 132721467 132721467 AAATACAGAACTTAGCTGGGTGTGTCGTGGGCATCTAGAGTCCCAGCTACTTGGGAGGCTGAGGT AAATACAGAACTTAGCTGGGTGTGTCGTGGGCTTCTAGAGTCCCAGCTACTTGGGAGGCTGAGGT A T PGAM5 Ensembl:ENSG00000247077 Protein coding 3'UTR GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs1487853155 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_415474,Human_RBP_ID_5256447,Human_RBP_ID_6154906,Human_RBP_ID_9013629,Human_RBP_ID_17813746,Human_RBP_ID_18257605,Human_RBP_ID_23157070,Human_RBP_ID_26414315,Human_RBP_ID_27420552 RMVar_hsa_circ_161854,RMVar_hsa_circ_92598 38842 RMVar_ID_38842 Human_SNP_ID_521434151 A-to-I Human chr12 + 132721688 132721688 132721688 TCGGCTCACCGCAACCTCTGCCTCCTGGGTTCAAGTGATTCTCCTGCCTCAGCTCCCGAGTAGCT TCGGCTCACCGCAACCTCTGCCTCCTGGGTTCGAGTGATTCTCCTGCCTCAGCTCCCGAGTAGCT A G PGAM5 Ensembl:ENSG00000247077 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs945261575 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_161854,RMVar_hsa_circ_92598 38843 RMVar_ID_38843 Human_SNP_ID_521434189 A-to-I Human chr12 + 132721831 132721831 132721831 TATAGAATTGTTCAGGCTGGTCTCGAACTCCCAACCTCAGGTGATTCACCCACCTTGGCCTCCCA TATAGAATTGTTCAGGCTGGTCTCGAACTCCCGACCTCAGGTGATTCACCCACCTTGGCCTCCCA A G PGAM5 Ensembl:ENSG00000247077 Protein coding 3'UTR GSE38233;GSE100210;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,29129909,31158229,32596459 RNA-Seq:(High) rs1191695270 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6154917,Human_RBP_ID_11883414,Human_RBP_ID_26423410,Human_RBP_ID_27420553 RMVar_hsa_circ_161854,RMVar_hsa_circ_92598 38844 RMVar_ID_38844 Human_SNP_ID_521434191 A-to-I Human chr12 + 132721837 132721837 132721837 ATTGTTCAGGCTGGTCTCGAACTCCCAACCTCAGGTGATTCACCCACCTTGGCCTCCCAAAGTGC ATTGTTCAGGCTGGTCTCGAACTCCCAACCTCGGGTGATTCACCCACCTTGGCCTCCCAAAGTGC A G PGAM5 Ensembl:ENSG00000247077 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-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 38845 RMVar_ID_38845 Human_SNP_ID_521434192 A-to-I Human chr12 + 132721842 132721842 132721842 TCAGGCTGGTCTCGAACTCCCAACCTCAGGTGATTCACCCACCTTGGCCTCCCAAAGTGCTGGGA TCAGGCTGGTCTCGAACTCCCAACCTCAGGTGGTTCACCCACCTTGGCCTCCCAAAGTGCTGGGA A G PGAM5 Ensembl:ENSG00000247077 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-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 38846 RMVar_ID_38846 Human_SNP_ID_521434412 A-to-I Human chr12 + 132722416 132722416 132722416 GGGATTATAGGCGCCCACCACCATGCCTGGCTAATTTTTTATTTTTAGTAGAGATGGGGTTTCAC GGGATTATAGGCGCCCACCACCATGCCTGGCTGATTTTTTATTTTTAGTAGAGATGGGGTTTCAC A G PGAM5 Ensembl:ENSG00000247077 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1142465 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_415488,Human_RBP_ID_6154944,Human_RBP_ID_17813755 RMVar_hsa_circ_161854,RMVar_hsa_circ_92598 38847 RMVar_ID_38847 Human_SNP_ID_521437707 A-to-I Human chr12 - 132731709 132731709 132731709 GCGTGGCGGCTCACACTATAATCCCAGCACTTAGGGAGGCCAACGTGGGTGGATTGCTGAAACCC GCGTGGCGGCTCACACTATAATCCCAGCACTTTGGGAGGCCAACGTGGGTGGATTGCTGAAACCC T A ANKLE2 Ensembl:ENSG00000176915 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1482837645 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24950869 RMVar_hsa_circ_16334,RMVar_hsa_circ_115866,RMVar_hsa_circ_79270,RMVar_hsa_circ_161861,RMVar_hsa_circ_161862,RMVar_hsa_circ_74067 38848 RMVar_ID_38848 Human_SNP_ID_521440121 A-to-I Human chr12 - 132737709 132737708 132737710 TAAAATATTACTTTTTTTTGTTTTTTTGAGACAGATTCTCACTCTGTCGCTCAGGCTGGAGTGCA TAAAATATTACTTTTTTTTGTTTTTTTGAGA__GATTCTCACTCTGTCGCTCAGGCTGGAGTGCA CTG C ANKLE2 Ensembl:ENSG00000176915 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs894135280 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_2314361 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 38849 RMVar_ID_38849 Human_SNP_ID_521440163 A-to-I Human chr12 - 132737879 132737879 132737879 TGGTGGCGCATGCCTGTGGTCCCAGCTACTCAAGAGGCTGAGGTGGGAGGATCCCTTGAGCCTGG TGGTGGCGCATGCCTGTGGTCCCAGCTACTCACGAGGCTGAGGTGGGAGGATCCCTTGAGCCTGG T G ANKLE2 Ensembl:ENSG00000176915 Protein coding intron GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line - 24183664,31158229 RNA-Seq:(High) rs1029111405 Functional Loss SNV dbSNP153 33..33 33 - - - 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 38850 RMVar_ID_38850 Human_SNP_ID_521440177 A-to-I Human chr12 - 132737920 132737920 132737920 GCAAGACCCCATCTCTACAAAAAGTAAAAATTAGCCGGGTGTGGTGGCGCATGCCTGTGGTCCCA GCAAGACCCCATCTCTACAAAAAGTAAAAATTGGCCGGGTGTGGTGGCGCATGCCTGTGGTCCCA T C ANKLE2 Ensembl:ENSG00000176915 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1446842197 Functional Loss SNV dbSNP153 33..33 33 - - - 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 38851 RMVar_ID_38851 Human_SNP_ID_521440178 A-to-I Human chr12 - 132737936 132737936 132737936 CAGCCTGGGCAACAGAGCAAGACCCCATCTCTACAAAAAGTAAAAATTAGCCGGGTGTGGTGGCG CAGCCTGGGCAACAGAGCAAGACCCCATCTCTGCAAAAAGTAAAAATTAGCCGGGTGTGGTGGCG T C ANKLE2 Ensembl:ENSG00000176915 Protein coding intron GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs1374248561 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23305756 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 38852 RMVar_ID_38852 Human_SNP_ID_521440203 A-to-I Human chr12 - 132738043 132738043 132738043 AAGCAGGACTGAGAAGCGAGGAGGCTGGGCACAGCGGCCCACACCTGTAATCCCAGAACTTTTGG AAGCAGGACTGAGAAGCGAGGAGGCTGGGCACGGCGGCCCACACCTGTAATCCCAGAACTTTTGG T C ANKLE2 Ensembl:ENSG00000176915 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1170348546 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26323780,Human_RBP_ID_26904526 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 38853 RMVar_ID_38853 Human_SNP_ID_521445813 A-to-I Human chr12 - 132755381 132755381 132755381 GCCACCACACCCGGCTAATTTTTTGTATTTTCAGTAGAGACGTGGTTTCACCATGTTGGCCGGGC GCCACCACACCCGGCTAATTTTTTGTATTTTCCGTAGAGACGTGGTTTCACCATGTTGGCCGGGC T G ANKLE2 Ensembl:ENSG00000176915 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1230029535 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11883893,Human_RBP_ID_24951047 38854 RMVar_ID_38854 Human_SNP_ID_521446184 A-to-I Human chr12 - 132756526 132756524 132756526 GCCATCTTTTTTTTTGTTGTTGTTGTTGAGACAGGGTCTGATTCTGTCACCCAGGCTGGAGTGCA GCCATCTTTTTTTTTGTTGTTGTTGTTGAGAC__GGTCTGATTCTGTCACCCAGGCTGGAGTGCA CCT C ANKLE2 Ensembl:ENSG00000176915 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1566039293 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_5127314,Human_RBP_ID_11883902,Human_RBP_ID_17561597,Human_RBP_ID_22472437 38855 RMVar_ID_38855 Human_SNP_ID_521446229 A-to-I Human chr12 - 132756671 132756671 132756671 CACCCACCTCGGTCTCCCAAAGTGCTGCGATTACAGGCGTGAGCCACCGCACCCGGCTTTACTTA CACCCACCTCGGTCTCCCAAAGTGCTGCGATTGCAGGCGTGAGCCACCGCACCCGGCTTTACTTA T C ANKLE2 Ensembl:ENSG00000176915 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1297159043 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11883909 38856 RMVar_ID_38856 Human_SNP_ID_521446277 A-to-I Human chr12 - 132756831 132756831 132756831 TGCCTCCTGGGTTCCAGCGAGTCTCCTGCCTCAGGTTCCCGAGTAGCTGGGATTACAGGTGCCCG TGCCTCCTGGGTTCCAGCGAGTCTCCTGCCTCGGGTTCCCGAGTAGCTGGGATTACAGGTGCCCG T C ANKLE2 Ensembl:ENSG00000176915 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334370658 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11883911 38857 RMVar_ID_38857 Human_SNP_ID_521446712 A-to-I Human chr12 - 132758244 132758244 132758244 CACCATGCCTGGCTAATTTTTGTGTTTTTAGTAGACACCTGGTTTCATCATGTTGGCCAGGCTGG CACCATGCCTGGCTAATTTTTGTGTTTTTAGTGGACACCTGGTTTCATCATGTTGGCCAGGCTGG T C ANKLE2 Ensembl:ENSG00000176915 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs530084766 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11883990 38858 RMVar_ID_38858 Human_SNP_ID_521446741 A-to-I Human chr12 - 132758389 132758389 132758389 TGCGACGTCCGCGGGTTTATTCTTTTTTTTTTAGGTGGAGTCTCACTCTGTTGTCCAGGCTGGAG TGCGACGTCCGCGGGTTTATTCTTTTTTTTTTGGGTGGAGTCTCACTCTGTTGTCCAGGCTGGAG T C ANKLE2 Ensembl:ENSG00000176915 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1373756336 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2314409,Human_RBP_ID_11883996 38859 RMVar_ID_38859 Human_SNP_ID_521447526 A-to-I Human chr12 - 132759899 132759899 132759899 GAATTCCTGACCTCAGGTGATCCACCTGCCTCAGCTTCCCAAAATGCTGGGATTACAGGTGTGAG GAATTCCTGACCTCAGGTGATCCACCTGCCTCGGCTTCCCAAAATGCTGGGATTACAGGTGTGAG T C ANKLE2 Ensembl:ENSG00000176915 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1262776948 Functional Loss SNV dbSNP153 33..33 33 - - - 38860 RMVar_ID_38860 Human_SNP_ID_521447527 A-to-I Human chr12 - 132759899 132759899 132759899 GAATTCCTGACCTCAGGTGATCCACCTGCCTCAGCTTCCCAAAATGCTGGGATTACAGGTGTGAG GAATTCCTGACCTCAGGTGATCCACCTGCCTCCGCTTCCCAAAATGCTGGGATTACAGGTGTGAG T G ANKLE2 Ensembl:ENSG00000176915 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1262776948 Functional Loss SNV dbSNP153 33..33 33 - - - 38861 RMVar_ID_38861 Human_SNP_ID_521451014 A-to-I Human chr12 - 132769661 132769661 132769661 GTTCATCCCCACACCGTGTGTCACAACAGGCTAGGGCACTTCACGATGTCACTACTTGTTTTTCT GTTCATCCCCACACCGTGTGTCACAACAGGCTGGGGCACTTCACGATGTCACTACTTGTTTTTCT T C GOLGA3 Ensembl:ENSG00000090615 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs978324998 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1791165,Human_RBP_ID_8370453,Human_RBP_ID_17357461 Human_miRNA_ID_2722266 RMVar_hsa_circ_76294,RMVar_hsa_circ_161875 38862 RMVar_ID_38862 Human_SNP_ID_521451141 A-to-I Human chr12 - 132770029 132770029 132770029 GAGTTCCACCATGTTGGCCAGGCTGGTCTTGAACTCTTGACCTCAGGTGATCCTGAGCCTCAGCC GAGTTCCACCATGTTGGCCAGGCTGGTCTTGATCTCTTGACCTCAGGTGATCCTGAGCCTCAGCC T A GOLGA3 Ensembl:ENSG00000090615 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1127077 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4214326,Human_RBP_ID_11884185,Human_RBP_ID_26414373 RMVar_hsa_circ_76294,RMVar_hsa_circ_161875 38863 RMVar_ID_38863 Human_SNP_ID_521451161 A-to-I Human chr12 - 132770098 132770098 132770098 CTCCCCAGTAGCTGGGATTACAGGTGCCCGCCACCACACCAGCCTAATTTTTGTATTTTTAGAGG CTCCCCAGTAGCTGGGATTACAGGTGCCCGCCGCCACACCAGCCTAATTTTTGTATTTTTAGAGG T C GOLGA3 Ensembl:ENSG00000090615 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs11545494 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2051968 RMVar_hsa_circ_76294,RMVar_hsa_circ_161875 38864 RMVar_ID_38864 Human_SNP_ID_521451165 A-to-I Human chr12 - 132770109 132770109 132770109 CCTGCCTCATTCTCCCCAGTAGCTGGGATTACAGGTGCCCGCCACCACACCAGCCTAATTTTTGT CCTGCCTCATTCTCCCCAGTAGCTGGGATTACTGGTGCCCGCCACCACACCAGCCTAATTTTTGT T A GOLGA3 Ensembl:ENSG00000090615 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1293615115 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1398848 RMVar_hsa_circ_76294,RMVar_hsa_circ_161875 38865 RMVar_ID_38865 Human_SNP_ID_521451183 A-to-I Human chr12 - 132770170 132770170 132770170 GGAGTGCAGTGGCGTGATCTCTGCTCACTGCAAGCTCCGCCATCTGGGTTCAAGCGATTCTCCTG GGAGTGCAGTGGCGTGATCTCTGCTCACTGCAGGCTCCGCCATCTGGGTTCAAGCGATTCTCCTG T C GOLGA3 Ensembl:ENSG00000090615 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs12809572 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27420598 RMVar_hsa_circ_76294,RMVar_hsa_circ_161875 38866 RMVar_ID_38866 Human_SNP_ID_521451381 A-to-I Human chr12 - 132770724 132770724 132770724 AGGCTGAGGCAGGAGAATCACTTGAACCCAGGAGGCGGAGCTTGCAGTGAGCCGAGATCGCGCCA AGGCTGAGGCAGGAGAATCACTTGAACCCAGGCGGCGGAGCTTGCAGTGAGCCGAGATCGCGCCA T G GOLGA3 Ensembl:ENSG00000090615 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1433623298 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76294,RMVar_hsa_circ_161875 38867 RMVar_ID_38867 Human_SNP_ID_521451384 A-to-I Human chr12 - 132770737 132770737 132770737 CCAGCTACTTGGGAGGCTGAGGCAGGAGAATCACTTGAACCCAGGAGGCGGAGCTTGCAGTGAGC CCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCAGGAGGCGGAGCTTGCAGTGAGC T C GOLGA3 Ensembl:ENSG00000090615 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1453575572 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76294,RMVar_hsa_circ_161875 38868 RMVar_ID_38868 Human_SNP_ID_521451397 A-to-I Human chr12 - 132770775 132770775 132770775 CAAAAATTAGCCGGGTGTCGTAGTGCGCACCTATAATCCCAGCTACTTGGGAGGCTGAGGCAGGA CAAAAATTAGCCGGGTGTCGTAGTGCGCACCTTTAATCCCAGCTACTTGGGAGGCTGAGGCAGGA T A GOLGA3 Ensembl:ENSG00000090615 Protein coding 3'UTR GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 29129909,30559470 RNA-Seq:(High) rs1262999333 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76294,RMVar_hsa_circ_161875 38869 RMVar_ID_38869 Human_SNP_ID_521451424 A-to-I Human chr12 - 132770853 132770853 132770853 AGGCGGGTGGATCACCTGAGGTCAAGAGGTCCAGACCATCCTGGCCAACATGGCAAAACCCCGTC AGGCGGGTGGATCACCTGAGGTCAAGAGGTCCGGACCATCCTGGCCAACATGGCAAAACCCCGTC T C GOLGA3 Ensembl:ENSG00000090615 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1566056574 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76294,RMVar_hsa_circ_161875 38870 RMVar_ID_38870 Human_SNP_ID_521451428 A-to-I Human chr12 - 132770861 132770861 132770861 GGAGGCCGAGGCGGGTGGATCACCTGAGGTCAAGAGGTCCAGACCATCCTGGCCAACATGGCAAA GGAGGCCGAGGCGGGTGGATCACCTGAGGTCAGGAGGTCCAGACCATCCTGGCCAACATGGCAAA T C GOLGA3 Ensembl:ENSG00000090615 Protein coding 3'UTR GSE100210;GSE107867 HepG2 cell line;ASD brains,temporal_cortex - 29129909,30559470 RNA-Seq:(High) rs1482854768 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76294,RMVar_hsa_circ_161875 38871 RMVar_ID_38871 Human_SNP_ID_521451447 A-to-I Human chr12 - 132770908 132770908 132770908 AAATCGGGCCGGGCGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGTGG AAATCGGGCCGGGCGCGGTGGCTCATGCCTGTGATCCCAGCACTTTGGGAGGCCGAGGCGGGTGG T C GOLGA3 Ensembl:ENSG00000090615 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs898600028 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76294,RMVar_hsa_circ_161875 38872 RMVar_ID_38872 Human_SNP_ID_521451849 A-to-I Human chr12 - 132772409 132772409 132772409 CTCTCGAGTAGCTGGGATTACAGGCGTGCGCCACTATGCCAGGCTAATGTTTGTATTTTTAGTAG CTCTCGAGTAGCTGGGATTACAGGCGTGCGCCCCTATGCCAGGCTAATGTTTGTATTTTTAGTAG T G GOLGA3 Ensembl:ENSG00000090615 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1314819655 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26421956 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 38873 RMVar_ID_38873 Human_SNP_ID_521451892 A-to-I Human chr12 - 132772500 132772500 132772500 TCGCTTTGTTGCCCAGGCTGGAGTGCAGTGGCACACTCTCCGCTCACTGCAAGCTCCGCCTCCCA TCGCTTTGTTGCCCAGGCTGGAGTGCAGTGGCGCACTCTCCGCTCACTGCAAGCTCCGCCTCCCA T C GOLGA3 Ensembl:ENSG00000090615 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1431601276 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12070352 Human_miRNA_ID_1770324,Human_miRNA_ID_2910423 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 38874 RMVar_ID_38874 Human_SNP_ID_521454229 A-to-I Human chr12 - 132778773 132778773 132778773 CTCCTGCCTCAGCCTCCCCAGTAGCTGGAACTACAGGCGTGCACCACCATGCCTGGCTAATTTTT CTCCTGCCTCAGCCTCCCCAGTAGCTGGAACTGCAGGCGTGCACCACCATGCCTGGCTAATTTTT T C GOLGA3 Ensembl:ENSG00000090615 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs867717165 Functional Loss SNV dbSNP153 33..33 33 - - - 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_268395,RMVar_hsa_circ_161880 38875 RMVar_ID_38875 Human_SNP_ID_521455866 A-to-I Human chr12 - 132783024 132783022 132783024 ACCTGGATAATTTCTGTAGTTTTGGTAGAGACAGGGTTTCATCATGTTGGCTAGGCTGGTCTCAA ACCTGGATAATTTCTGTAGTTTTGGTAGAGAC__GGTTTCATCATGTTGGCTAGGCTGGTCTCAA CCT C GOLGA3 Ensembl:ENSG00000090615 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs931843293 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_11884423 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_161885 38876 RMVar_ID_38876 Human_SNP_ID_521456089 A-to-I Human chr12 - 132783674 132783674 132783674 ACTTGGGTGGCTGAGGCAGGTAAACCGCTTGAACCCAGGAGCGGAGGTTGCAGTGAGCCAAGATC ACTTGGGTGGCTGAGGCAGGTAAACCGCTTGACCCCAGGAGCGGAGGTTGCAGTGAGCCAAGATC T G GOLGA3 Ensembl:ENSG00000090615 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1382237045 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17561353 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_161885 38877 RMVar_ID_38877 Human_SNP_ID_521456114 A-to-I Human chr12 - 132783771 132783765 132783772 GAGCTCGAGACCAGCCTGGCCGACATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCC GAGCTCGAGACCAGCCTGGCCGACATGGTGA_______TCTCTACTAAAAATACAAAAATTAGCC ATGGGGTT A GOLGA3 Ensembl:ENSG00000090615 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1360999996 Functional Loss DEL dbSNP153 32..38 33 - - - 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_161885 38878 RMVar_ID_38878 Human_SNP_ID_521456168 A-to-I Human chr12 - 132783944 132783944 132783944 GGGGAGGATCACTGTACAGCCTCTTTGGTGGAATGGTTACAGAATTCATAGTGGAACCCTTCTCA GGGGAGGATCACTGTACAGCCTCTTTGGTGGAGTGGTTACAGAATTCATAGTGGAACCCTTCTCA T C GOLGA3 Ensembl:ENSG00000090615 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11147073 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22040242,Human_RBP_ID_22573981 GWAS_ID_4388,GWAS_ID_4389,GWAS_ID_4390,GWAS_ID_4391 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_161885 38879 RMVar_ID_38879 Human_SNP_ID_521461724 A-to-I Human chr12 - 132799556 132799553 132799557 AGCTCCCTGCAGCCTTGACCTGTTGGGCTCAAACAGTCCTCCTGCCTCAGCCCCCCAAGTAGCTG AGCTCCCTGCAGCCTTGACCTGTTGGGCTCA____GTCCTCCTGCCTCAGCCCCCCAAGTAGCTG CTGTT C GOLGA3 Ensembl:ENSG00000090615 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs151327943 Functional Loss DEL dbSNP153 32..35 33 - - - 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_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_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_161895,RMVar_hsa_circ_161896 38880 RMVar_ID_38880 Human_SNP_ID_521461817 A-to-I Human chr12 - 132799809 132799809 132799809 TTGAATCCAGGAGGCAGAGGTTGTAGTGAGCCAAGATTGCGCTGCTGCACTCCACACTTCAGCCT TTGAATCCAGGAGGCAGAGGTTGTAGTGAGCCGAGATTGCGCTGCTGCACTCCACACTTCAGCCT T C GOLGA3 Ensembl:ENSG00000090615 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1048917168 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_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_161895,RMVar_hsa_circ_161896 38881 RMVar_ID_38881 Human_SNP_ID_521461935 A-to-I Human chr12 - 132800261 132800261 132800261 TTGAACTCTTGACCTTGTGATCCGCCTTCCTCAGCCTTCCAGAGTGCTGGGATTACAGGTGTGAG TTGAACTCTTGACCTTGTGATCCGCCTTCCTCGGCCTTCCAGAGTGCTGGGATTACAGGTGTGAG T C GOLGA3 Ensembl:ENSG00000090615 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs550375990 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_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_161895,RMVar_hsa_circ_161896 38882 RMVar_ID_38882 Human_SNP_ID_521461992 A-to-I Human chr12 - 132800442 132800442 132800442 TCTCCCAGGCTGGAGTACAGTGTTGTGATCTCAGCTCACTGCAACCTCTGTCTCCTGGGTTCAAG TCTCCCAGGCTGGAGTACAGTGTTGTGATCTCGGCTCACTGCAACCTCTGTCTCCTGGGTTCAAG T C GOLGA3 Ensembl:ENSG00000090615 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6560905 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_4392,GWAS_ID_4393,GWAS_ID_4394,GWAS_ID_4395,GWAS_ID_4396,GWAS_ID_4397,GWAS_ID_4398,GWAS_ID_4399,GWAS_ID_4400,GWAS_ID_4401 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_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_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_161895,RMVar_hsa_circ_161896 38883 RMVar_ID_38883 Human_SNP_ID_521468059 A-to-I Human chr12 - 132818298 132818298 132818298 CTGAGCTTGTGTGACTGAACTCCAGCCTGGGCAGCAGAATGAGACTCCGTCTCAAAAAAGAGAAG CTGAGCTTGTGTGACTGAACTCCAGCCTGGGCGGCAGAATGAGACTCCGTCTCAAAAAAGAGAAG T C GOLGA3 Ensembl:ENSG00000090615 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1415841782 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11884895 RMVar_hsa_circ_3416,RMVar_hsa_circ_340011,RMVar_hsa_circ_84355,RMVar_hsa_circ_161887,RMVar_hsa_circ_361935,RMVar_hsa_circ_51099,RMVar_hsa_circ_296106,RMVar_hsa_circ_101119,RMVar_hsa_circ_161898,RMVar_hsa_circ_161896,RMVar_hsa_circ_351290,RMVar_hsa_circ_320947,RMVar_hsa_circ_161900,RMVar_hsa_circ_276865,RMVar_hsa_circ_161902,RMVar_hsa_circ_51000,RMVar_hsa_circ_310624,RMVar_hsa_circ_161905,RMVar_hsa_circ_326501 38884 RMVar_ID_38884 Human_SNP_ID_521468106 A-to-I Human chr12 - 132818464 132818464 132818464 GAATGGGGAGGAGTTTGAGACCAGACTGGCCAACATGGTGAAACCCCATCTCTACTAAAAAGACC GAATGGGGAGGAGTTTGAGACCAGACTGGCCAGCATGGTGAAACCCCATCTCTACTAAAAAGACC T C GOLGA3 Ensembl:ENSG00000090615 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1271279932 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3416,RMVar_hsa_circ_340011,RMVar_hsa_circ_84355,RMVar_hsa_circ_161887,RMVar_hsa_circ_361935,RMVar_hsa_circ_51099,RMVar_hsa_circ_296106,RMVar_hsa_circ_101119,RMVar_hsa_circ_161898,RMVar_hsa_circ_161896,RMVar_hsa_circ_351290,RMVar_hsa_circ_320947,RMVar_hsa_circ_161900,RMVar_hsa_circ_276865,RMVar_hsa_circ_161902,RMVar_hsa_circ_51000,RMVar_hsa_circ_310624,RMVar_hsa_circ_161905,RMVar_hsa_circ_326501 38885 RMVar_ID_38885 Human_SNP_ID_521476520 A-to-I Human chr12 - 132844905 132844905 132844905 TGTGGGGCCGGGCGTGGAGGCTCACGCCTGTAATCCCAGCATTTTGGGAAGCCGAGGCGGGCGGA TGTGGGGCCGGGCGTGGAGGCTCACGCCTGTAGTCCCAGCATTTTGGGAAGCCGAGGCGGGCGGA T C CHFR Ensembl:ENSG00000072609 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973431370 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126452,RMVar_hsa_circ_43486,RMVar_hsa_circ_28401,RMVar_hsa_circ_161908,RMVar_hsa_circ_290207,RMVar_hsa_circ_161910,RMVar_hsa_circ_292668,RMVar_hsa_circ_297491,RMVar_hsa_circ_343035,RMVar_hsa_circ_270875,RMVar_hsa_circ_161911,RMVar_hsa_circ_161913,RMVar_hsa_circ_161914,RMVar_hsa_circ_161912 38886 RMVar_ID_38886 Human_SNP_ID_521476720 A-to-I Human chr12 - 132845528 132845528 132845528 ATCTCACCTCAGCCTCCCAAGTAGCTGGGACCACAAGCGTGTGCTACCATGCCTGGCTAATCTTA ATCTCACCTCAGCCTCCCAAGTAGCTGGGACCGCAAGCGTGTGCTACCATGCCTGGCTAATCTTA T C CHFR Ensembl:ENSG00000072609 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1360175069 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126452,RMVar_hsa_circ_43486,RMVar_hsa_circ_28401,RMVar_hsa_circ_161908,RMVar_hsa_circ_290207,RMVar_hsa_circ_161910,RMVar_hsa_circ_292668,RMVar_hsa_circ_297491,RMVar_hsa_circ_343035,RMVar_hsa_circ_270875,RMVar_hsa_circ_161911,RMVar_hsa_circ_161913,RMVar_hsa_circ_161914,RMVar_hsa_circ_161912 38887 RMVar_ID_38887 Human_SNP_ID_521476740 A-to-I Human chr12 - 132845598 132845598 132845598 TCGCCCAGGCTGGAGTGCAGGGGCATGATCACAGCTCACTGCAGCCTCGACCTCCTGGGCTCAAG TCGCCCAGGCTGGAGTGCAGGGGCATGATCACGGCTCACTGCAGCCTCGACCTCCTGGGCTCAAG T C CHFR Ensembl:ENSG00000072609 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1398571267 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126452,RMVar_hsa_circ_43486,RMVar_hsa_circ_28401,RMVar_hsa_circ_161908,RMVar_hsa_circ_290207,RMVar_hsa_circ_161910,RMVar_hsa_circ_292668,RMVar_hsa_circ_297491,RMVar_hsa_circ_343035,RMVar_hsa_circ_270875,RMVar_hsa_circ_161911,RMVar_hsa_circ_161913,RMVar_hsa_circ_161914,RMVar_hsa_circ_161912 38888 RMVar_ID_38888 Human_SNP_ID_521477127 A-to-I Human chr12 - 132846828 132846828 132846828 TTGCCCAGACTGGAGTGCAGTGGCATGATCTCAGCTCAAGGCCCCCTCGGCCTCCTGGGTTCAAG TTGCCCAGACTGGAGTGCAGTGGCATGATCTCGGCTCAAGGCCCCCTCGGCCTCCTGGGTTCAAG T C CHFR Ensembl:ENSG00000072609 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1008782387 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126452,RMVar_hsa_circ_43486,RMVar_hsa_circ_28401,RMVar_hsa_circ_161908,RMVar_hsa_circ_290207,RMVar_hsa_circ_161910,RMVar_hsa_circ_292668,RMVar_hsa_circ_297491,RMVar_hsa_circ_343035,RMVar_hsa_circ_270875,RMVar_hsa_circ_161911,RMVar_hsa_circ_161913,RMVar_hsa_circ_161914,RMVar_hsa_circ_161912 38889 RMVar_ID_38889 Human_SNP_ID_521482393 A-to-I Human chr12 - 132863844 132863844 132863844 AGAGGTGGAAGGATCGCTTTAGCCCAGGAGGCAGAGGTTGCAGTGAATGAAGATCTCGCCACTGC AGAGGTGGAAGGATCGCTTTAGCCCAGGAGGCGGAGGTTGCAGTGAATGAAGATCTCGCCACTGC T C CHFR Ensembl:ENSG00000072609 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1160715183 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27889,RMVar_hsa_circ_126452,RMVar_hsa_circ_161908,RMVar_hsa_circ_292668,RMVar_hsa_circ_161914,RMVar_hsa_circ_35755,RMVar_hsa_circ_337384,RMVar_hsa_circ_41819,RMVar_hsa_circ_337153,RMVar_hsa_circ_366419,RMVar_hsa_circ_291817,RMVar_hsa_circ_161925 38890 RMVar_ID_38890 Human_SNP_ID_521482394 A-to-I Human chr12 - 132863851 132863851 132863851 AGGAGGCAGAGGTGGAAGGATCGCTTTAGCCCAGGAGGCAGAGGTTGCAGTGAATGAAGATCTCG AGGAGGCAGAGGTGGAAGGATCGCTTTAGCCCGGGAGGCAGAGGTTGCAGTGAATGAAGATCTCG T C CHFR Ensembl:ENSG00000072609 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1420471000 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27889,RMVar_hsa_circ_126452,RMVar_hsa_circ_161908,RMVar_hsa_circ_292668,RMVar_hsa_circ_161914,RMVar_hsa_circ_35755,RMVar_hsa_circ_337384,RMVar_hsa_circ_41819,RMVar_hsa_circ_337153,RMVar_hsa_circ_366419,RMVar_hsa_circ_291817,RMVar_hsa_circ_161925 38891 RMVar_ID_38891 Human_SNP_ID_521482851 A-to-I Human chr12 - 132865529 132865529 132865529 GTCTCTACTGAAAATACAAAAATTATCCAGGCATGGTGGCAGGCGCCTGTAGTCCCAGCTACTCA GTCTCTACTGAAAATACAAAAATTATCCAGGCGTGGTGGCAGGCGCCTGTAGTCCCAGCTACTCA T C CHFR Ensembl:ENSG00000072609 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1280873793 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27889,RMVar_hsa_circ_126452,RMVar_hsa_circ_161908,RMVar_hsa_circ_292668,RMVar_hsa_circ_161914,RMVar_hsa_circ_35755,RMVar_hsa_circ_337384,RMVar_hsa_circ_41819,RMVar_hsa_circ_337153,RMVar_hsa_circ_366419,RMVar_hsa_circ_291817,RMVar_hsa_circ_161925 38892 RMVar_ID_38892 Human_SNP_ID_521482926 A-to-I Human chr12 - 132865735 132865735 132865735 GGATTGCCTGAGCCTGGGAGGCAGAGGTTACAATGTGCTGAGATTGCACCACTGCACTCCAGCCT GGATTGCCTGAGCCTGGGAGGCAGAGGTTACAGTGTGCTGAGATTGCACCACTGCACTCCAGCCT T C CHFR Ensembl:ENSG00000072609 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs922610792 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9671761 RMVar_hsa_circ_27889,RMVar_hsa_circ_126452,RMVar_hsa_circ_161908,RMVar_hsa_circ_292668,RMVar_hsa_circ_161914,RMVar_hsa_circ_35755,RMVar_hsa_circ_337384,RMVar_hsa_circ_41819,RMVar_hsa_circ_337153,RMVar_hsa_circ_366419,RMVar_hsa_circ_291817,RMVar_hsa_circ_161925 38893 RMVar_ID_38893 Human_SNP_ID_521487127 A-to-I Human chr12 - 132878456 132878456 132878456 CTTTTTTTTTTTTTTATTTCCAGTTGGAGTCTAGCTCTGTCGCCAAGGCTGGAGTGCAGTGGCGC CTTTTTTTTTTTTTTATTTCCAGTTGGAGTCTTGCTCTGTCGCCAAGGCTGGAGTGCAGTGGCGC T A CHFR Ensembl:ENSG00000072609 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1185638372 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11885743 RMVar_hsa_circ_27889,RMVar_hsa_circ_45346 38894 RMVar_ID_38894 Human_SNP_ID_521515450 A-to-I Human chr12 + 132990097 132990097 132990097 CTTTAGCCTAGGAATTCAGGACCAGCCTGGGCAACATAGTGAGACCCCATCTCTACAAAAAATTA CTTTAGCCTAGGAATTCAGGACCAGCCTGGGCGACATAGTGAGACCCCATCTCTACAAAAAATTA A G ZNF26 Ensembl:ENSG00000198393 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1217527097 Functional Loss SNV dbSNP153 33..33 33 - - - 38895 RMVar_ID_38895 Human_SNP_ID_521526403 A-to-I Human chr12 + 133040304 133040304 133040304 AATGCTGAAGCCAGGTGTGGTGTTGTATGCCTATAATCCTAGCACTCTGGGAGGCTGAGGTGGGA AATGCTGAAGCCAGGTGTGGTGTTGTATGCCTGTAATCCTAGCACTCTGGGAGGCTGAGGTGGGA A G ZNF84 Ensembl:ENSG00000198040 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs878987642 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24951697 RMVar_hsa_circ_25950 38896 RMVar_ID_38896 Human_SNP_ID_521536409 A-to-I Human chr12 + 133085166 133085166 133085166 GCTGCTTCAGCCCCCTGAGTAACTGGGACTACAGGCACCTGCCACCATGCCTGGCTAAGTTTTGT GCTGCTTCAGCCCCCTGAGTAACTGGGACTACGGGCACCTGCCACCATGCCTGGCTAAGTTTTGT A G ZNF140 Ensembl:ENSG00000196387 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs912787738 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_161927,RMVar_hsa_circ_96113,RMVar_hsa_circ_161928,RMVar_hsa_circ_98940 38897 RMVar_ID_38897 Human_SNP_ID_521539877 A-to-I Human chr12 + 133097388 133097388 133097388 ATTTTTGGCTGGGTGTGGTGGCTCACGCCTGTAATCCTGGCACTATGGGAGGCCAAGGTGGGCAG ATTTTTGGCTGGGTGTGGTGGCTCACGCCTGTTATCCTGGCACTATGGGAGGCCAAGGTGGGCAG A T ZNF140 Ensembl:ENSG00000196387 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs938236417 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_161927,RMVar_hsa_circ_96113,RMVar_hsa_circ_161928,RMVar_hsa_circ_98940 38898 RMVar_ID_38898 Human_SNP_ID_521541447 A-to-I Human chr12 + 133103510 133103510 133103510 GTTGTTTAGGCTGGTCTCAAACTCTAGGACTCAAGTGATCCTCCAGCCTCAGCCTCCCAAAGTTG GTTGTTTAGGCTGGTCTCAAACTCTAGGACTCGAGTGATCCTCCAGCCTCAGCCTCCCAAAGTTG A G ZNF140 Ensembl:ENSG00000196387 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1485429650 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_161927,RMVar_hsa_circ_96113,RMVar_hsa_circ_161928,RMVar_hsa_circ_98940 38899 RMVar_ID_38899 Human_SNP_ID_521544712 A-to-I Human chr12 - 133116233 133116233 133116233 AAGTGTGGTGGTGGGCGCCTGTAGTACCAGCTACTCGGGAGGCTGAGGCAGGAGAATGCTGTGAA AAGTGTGGTGGTGGGCGCCTGTAGTACCAGCTGCTCGGGAGGCTGAGGCAGGAGAATGCTGTGAA T C ZNF891 Ensembl:ENSG00000214029 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs974440471 Functional Loss SNV dbSNP153 33..33 33 - - - 38900 RMVar_ID_38900 Human_SNP_ID_521545192 A-to-I Human chr12 - 133118161 133118161 133118161 CTGAGGCAGGCGGATCACAAGGTCAGATCGAGACCATCCTGGCCAACATGGTGAAACCCTGGTTC CTGAGGCAGGCGGATCACAAGGTCAGATCGAGCCCATCCTGGCCAACATGGTGAAACCCTGGTTC T G ZNF891 Ensembl:ENSG00000214029 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992674731 Functional Loss SNV dbSNP153 33..33 33 - - - 38901 RMVar_ID_38901 Human_SNP_ID_579652781 A-to-I Human chr15 - 60376585 60376585 60376585 GGCTACTTTTCCCAGCCAGTCTGCCTCCTGGCACCCTCGAGAGAATATATTCCTAATTGCTGTGC GGCTACTTTTCCCAGCCAGTCTGCCTCCTGGCGCCCTCGAGAGAATATATTCCTAATTGCTGTGC T C ANXA2 Ensembl:ENSG00000182718 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1308269031 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_172567,RMVar_hsa_circ_307579,RMVar_hsa_circ_346419,RMVar_hsa_circ_172568,RMVar_hsa_circ_277326 38902 RMVar_ID_38902 Human_SNP_ID_579652792 A-to-I Human chr15 - 60376627 60376627 60376627 GAGCTAAAGCTCCTCACTTGCAGCCCTCTGTTAGAGGAGAGAGGCTACTTTTCCCAGCCAGTCTG GAGCTAAAGCTCCTCACTTGCAGCCCTCTGTTGGAGGAGAGAGGCTACTTTTCCCAGCCAGTCTG T C ANXA2 Ensembl:ENSG00000182718 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1445889243 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_172567,RMVar_hsa_circ_307579,RMVar_hsa_circ_346419,RMVar_hsa_circ_172568,RMVar_hsa_circ_277326 38903 RMVar_ID_38903 Human_SNP_ID_579656292 A-to-I Human chr15 - 60388896 60388896 60388896 TTATCTCTACTGGAAAAAAAAAAGCCAGGTGTAGTGGCACACGCCTGTAGTCCCAGCTACTTGGG TTATCTCTACTGGAAAAAAAAAAGCCAGGTGTGGTGGCACACGCCTGTAGTCCCAGCTACTTGGG T C ANXA2 Ensembl:ENSG00000182718 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232257407 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124678,RMVar_hsa_circ_172550,RMVar_hsa_circ_2198,RMVar_hsa_circ_52898,RMVar_hsa_circ_47446,RMVar_hsa_circ_117179,RMVar_hsa_circ_91465,RMVar_hsa_circ_172571,RMVar_hsa_circ_172572 38904 RMVar_ID_38904 Human_SNP_ID_579665807 A-to-I Human chr15 - 60422224 60422224 60422224 AAAGGCTGAGGCAGAAGAATTGCTTGAGCCCAAGAAGTCAAGGCTACAGTGAGTTGTGATCGCAC AAAGGCTGAGGCAGAAGAATTGCTTGAGCCCAGGAAGTCAAGGCTACAGTGAGTTGTGATCGCAC T C ICE2 Ensembl:ENSG00000128915 Protein coding 3'UTR GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,29796672,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs1477467456 Functional Loss SNV dbSNP153 33..33 33 - - - 38905 RMVar_ID_38905 Human_SNP_ID_579665815 A-to-I Human chr15 - 60422248 60422248 60422248 TGTGCCTGTAGTCCCAGCTACTCAAAAGGCTGAGGCAGAAGAATTGCTTGAGCCCAAGAAGTCAA TGTGCCTGTAGTCCCAGCTACTCAAAAGGCTGGGGCAGAAGAATTGCTTGAGCCCAAGAAGTCAA T C ICE2 Ensembl:ENSG00000128915 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1409543587 Functional Loss SNV dbSNP153 33..33 33 - - - 38906 RMVar_ID_38906 Human_SNP_ID_579665835 A-to-I Human chr15 - 60422297 60422297 60422297 ACACAGACCTCATCTCTACAAATAAAAAAGTTAGCCGGGTGTGGTGGGGTGTGCCTGTAGTCCCA ACACAGACCTCATCTCTACAAATAAAAAAGTTGGCCGGGTGTGGTGGGGTGTGCCTGTAGTCCCA T C ICE2 Ensembl:ENSG00000128915 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1410503067 Functional Loss SNV dbSNP153 33..33 33 - - - 38907 RMVar_ID_38907 Human_SNP_ID_579665837 A-to-I Human chr15 - 60422301 60422301 60422301 GGCAACACAGACCTCATCTCTACAAATAAAAAAGTTAGCCGGGTGTGGTGGGGTGTGCCTGTAGT GGCAACACAGACCTCATCTCTACAAATAAAAACGTTAGCCGGGTGTGGTGGGGTGTGCCTGTAGT T G ICE2 Ensembl:ENSG00000128915 Protein coding 3'UTR GSE47997;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,31158229,31158229,31158229 RNA-Seq:(High) rs892124382 Functional Loss SNV dbSNP153 33..33 33 - - - 38908 RMVar_ID_38908 Human_SNP_ID_579665838 A-to-I Human chr15 - 60422302 60422302 60422302 GGGCAACACAGACCTCATCTCTACAAATAAAAAAGTTAGCCGGGTGTGGTGGGGTGTGCCTGTAG GGGCAACACAGACCTCATCTCTACAAATAAAACAGTTAGCCGGGTGTGGTGGGGTGTGCCTGTAG T G ICE2 Ensembl:ENSG00000128915 Protein coding 3'UTR GSE47997;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;Bronchiolar epithelium,BERP35T1 cell line - 23474544,31158229 RNA-Seq:(High) rs1009217117 Functional Loss SNV dbSNP153 33..33 33 - - - 38909 RMVar_ID_38909 Human_SNP_ID_579665854 A-to-I Human chr15 - 60422353 60422353 60422353 GCAAGGCCGAGGCGGGAGAATCACTTGAGTCCAGGGGTTGGAGACCAGTCTGGGCAACACAGACC GCAAGGCCGAGGCGGGAGAATCACTTGAGTCCGGGGGTTGGAGACCAGTCTGGGCAACACAGACC T C ICE2 Ensembl:ENSG00000128915 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1351395470 Functional Loss SNV dbSNP153 33..33 33 - - - 38910 RMVar_ID_38910 Human_SNP_ID_579665945 A-to-I Human chr15 - 60422669 60422669 60422669 AGGCTTGGCTAATTTTTTTTTGTATTTTTAGTAGAGACAGGGTGTTACCATGTTGGCCGGGCTGG AGGCTTGGCTAATTTTTTTTTGTATTTTTAGTGGAGACAGGGTGTTACCATGTTGGCCGGGCTGG T C ICE2 Ensembl:ENSG00000128915 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1393613213 Functional Loss SNV dbSNP153 33..33 33 - - - 38911 RMVar_ID_38911 Human_SNP_ID_579670350 A-to-I Human chr15 - 60437460 60437460 60437460 AGGCCTGGTGGTGGGCACCTGTAATCCCATCTACTCGGCAGGCTGAGGCAGGATCGCTTGAACTG AGGCCTGGTGGTGGGCACCTGTAATCCCATCTGCTCGGCAGGCTGAGGCAGGATCGCTTGAACTG T C ICE2 Ensembl:ENSG00000128915 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053345461 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59328,RMVar_hsa_circ_3780,RMVar_hsa_circ_336257,RMVar_hsa_circ_373009,RMVar_hsa_circ_373940,RMVar_hsa_circ_7054,RMVar_hsa_circ_83316,RMVar_hsa_circ_172573,RMVar_hsa_circ_172574,RMVar_hsa_circ_172575,RMVar_hsa_circ_301174,RMVar_hsa_circ_333628,RMVar_hsa_circ_97931,RMVar_hsa_circ_60930,RMVar_hsa_circ_172577,RMVar_hsa_circ_3167,RMVar_hsa_circ_172576,RMVar_hsa_circ_336974,RMVar_hsa_circ_59512,RMVar_hsa_circ_172578,RMVar_hsa_circ_45426,RMVar_hsa_circ_49104,RMVar_hsa_circ_44750 38912 RMVar_ID_38912 Human_SNP_ID_579670435 A-to-I Human chr15 - 60437720 60437720 60437720 TTGAACCCCGGAGGTGGAGGTTACAGTGAGCCAGGATCTCGCTGCTGCACTCCAGCCCAGGAGAC TTGAACCCCGGAGGTGGAGGTTACAGTGAGCCGGGATCTCGCTGCTGCACTCCAGCCCAGGAGAC T C ICE2 Ensembl:ENSG00000128915 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1257063826 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59328,RMVar_hsa_circ_3780,RMVar_hsa_circ_336257,RMVar_hsa_circ_373009,RMVar_hsa_circ_373940,RMVar_hsa_circ_7054,RMVar_hsa_circ_83316,RMVar_hsa_circ_172573,RMVar_hsa_circ_172574,RMVar_hsa_circ_172575,RMVar_hsa_circ_301174,RMVar_hsa_circ_333628,RMVar_hsa_circ_97931,RMVar_hsa_circ_60930,RMVar_hsa_circ_172577,RMVar_hsa_circ_3167,RMVar_hsa_circ_172576,RMVar_hsa_circ_336974,RMVar_hsa_circ_59512,RMVar_hsa_circ_172578,RMVar_hsa_circ_45426,RMVar_hsa_circ_49104,RMVar_hsa_circ_44750 38913 RMVar_ID_38913 Human_SNP_ID_579672216 A-to-I Human chr15 - 60444796 60444796 60444796 CATATAAACCTGGCTGCTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCAGGAGGTGGAAGTT CATATAAACCTGGCTGCTCGGGAGGCTGAGGCGGGAGAATCGCTTGAACCCAGGAGGTGGAAGTT T C ICE2 Ensembl:ENSG00000128915 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs936168024 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1311,RMVar_hsa_circ_59328,RMVar_hsa_circ_3780,RMVar_hsa_circ_336257,RMVar_hsa_circ_373009,RMVar_hsa_circ_373940,RMVar_hsa_circ_83316,RMVar_hsa_circ_172573,RMVar_hsa_circ_172574,RMVar_hsa_circ_172575,RMVar_hsa_circ_333628,RMVar_hsa_circ_97931,RMVar_hsa_circ_60930,RMVar_hsa_circ_172577,RMVar_hsa_circ_3167,RMVar_hsa_circ_172576,RMVar_hsa_circ_59512,RMVar_hsa_circ_172578,RMVar_hsa_circ_45426,RMVar_hsa_circ_49104,RMVar_hsa_circ_300381,RMVar_hsa_circ_336943,RMVar_hsa_circ_362636,RMVar_hsa_circ_364087,RMVar_hsa_circ_328490,RMVar_hsa_circ_110544,RMVar_hsa_circ_127591,RMVar_hsa_circ_57505,RMVar_hsa_circ_172579,RMVar_hsa_circ_172581,RMVar_hsa_circ_172582,RMVar_hsa_circ_172580 38914 RMVar_ID_38914 Human_SNP_ID_579672218 A-to-I Human chr15 - 60444800 60444800 60444800 TGCACATATAAACCTGGCTGCTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCAGGAGGTGGA TGCACATATAAACCTGGCTGCTCGGGAGGCTGCGGCAGGAGAATCGCTTGAACCCAGGAGGTGGA T G ICE2 Ensembl:ENSG00000128915 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs555995400 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1311,RMVar_hsa_circ_59328,RMVar_hsa_circ_3780,RMVar_hsa_circ_336257,RMVar_hsa_circ_373009,RMVar_hsa_circ_373940,RMVar_hsa_circ_83316,RMVar_hsa_circ_172573,RMVar_hsa_circ_172574,RMVar_hsa_circ_172575,RMVar_hsa_circ_333628,RMVar_hsa_circ_97931,RMVar_hsa_circ_60930,RMVar_hsa_circ_172577,RMVar_hsa_circ_3167,RMVar_hsa_circ_172576,RMVar_hsa_circ_59512,RMVar_hsa_circ_172578,RMVar_hsa_circ_45426,RMVar_hsa_circ_49104,RMVar_hsa_circ_300381,RMVar_hsa_circ_336943,RMVar_hsa_circ_362636,RMVar_hsa_circ_364087,RMVar_hsa_circ_328490,RMVar_hsa_circ_110544,RMVar_hsa_circ_127591,RMVar_hsa_circ_57505,RMVar_hsa_circ_172579,RMVar_hsa_circ_172581,RMVar_hsa_circ_172582,RMVar_hsa_circ_172580 38915 RMVar_ID_38915 Human_SNP_ID_579674381 A-to-I Human chr15 - 60452606 60452606 60452606 ATTGTTTATAGAGAACTTGATTCATTCATTCCATAAGTTTTTATTAAGCAGATACTATTCTATGC ATTGTTTATAGAGAACTTGATTCATTCATTCCGTAAGTTTTTATTAAGCAGATACTATTCTATGC T C ICE2 Ensembl:ENSG00000128915 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs541048050 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12543975,Human_RBP_ID_25149254 RMVar_hsa_circ_1311,RMVar_hsa_circ_3780,RMVar_hsa_circ_373009,RMVar_hsa_circ_172575,RMVar_hsa_circ_97931,RMVar_hsa_circ_60930,RMVar_hsa_circ_3167,RMVar_hsa_circ_172576,RMVar_hsa_circ_59512,RMVar_hsa_circ_49104,RMVar_hsa_circ_300381,RMVar_hsa_circ_336943,RMVar_hsa_circ_362636,RMVar_hsa_circ_328490,RMVar_hsa_circ_57505,RMVar_hsa_circ_17429,RMVar_hsa_circ_172581,RMVar_hsa_circ_172582,RMVar_hsa_circ_378962,RMVar_hsa_circ_40063,RMVar_hsa_circ_125158,RMVar_hsa_circ_68735,RMVar_hsa_circ_89602,RMVar_hsa_circ_172583,RMVar_hsa_circ_172584,RMVar_hsa_circ_172585 38916 RMVar_ID_38916 Human_SNP_ID_579677565 A-to-I Human chr15 - 60462957 60462957 60462957 TTGCAATGGTTTGGCACCATCATAAATTTGGAAAATCATTTAGTGGAACCTTCATAAGTTGGGAA TTGCAATGGTTTGGCACCATCATAAATTTGGAGAATCATTTAGTGGAACCTTCATAAGTTGGGAA T C ICE2 Ensembl:ENSG00000128915 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1440031615 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3478053,Human_RBP_ID_8419625,Human_RBP_ID_18280582,Human_RBP_ID_18664970,Human_RBP_ID_23658298 RMVar_hsa_circ_1311,RMVar_hsa_circ_60930,RMVar_hsa_circ_300381,RMVar_hsa_circ_328490,RMVar_hsa_circ_57505,RMVar_hsa_circ_8346,RMVar_hsa_circ_17429,RMVar_hsa_circ_172582,RMVar_hsa_circ_378962,RMVar_hsa_circ_68735,RMVar_hsa_circ_273585,RMVar_hsa_circ_350875,RMVar_hsa_circ_73564,RMVar_hsa_circ_73653,RMVar_hsa_circ_172586,RMVar_hsa_circ_301585,RMVar_hsa_circ_61667,RMVar_hsa_circ_343997 38917 RMVar_ID_38917 Human_SNP_ID_579677787 A-to-I Human chr15 - 60463718 60463718 60463718 TCGCCCAGGCTAGAGTGCAATGGCACGATCTCAGCCCACTGCAACCTCTGCCTCCAGGGTTCAAG TCGCCCAGGCTAGAGTGCAATGGCACGATCTCGGCCCACTGCAACCTCTGCCTCCAGGGTTCAAG T C ICE2 Ensembl:ENSG00000128915 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968907705 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1311,RMVar_hsa_circ_60930,RMVar_hsa_circ_300381,RMVar_hsa_circ_328490,RMVar_hsa_circ_57505,RMVar_hsa_circ_8346,RMVar_hsa_circ_17429,RMVar_hsa_circ_172582,RMVar_hsa_circ_378962,RMVar_hsa_circ_68735,RMVar_hsa_circ_273585,RMVar_hsa_circ_350875,RMVar_hsa_circ_73564,RMVar_hsa_circ_73653,RMVar_hsa_circ_172586,RMVar_hsa_circ_301585,RMVar_hsa_circ_61667,RMVar_hsa_circ_343997 38918 RMVar_ID_38918 Human_SNP_ID_579678129 A-to-I Human chr15 - 60464783 60464783 60464783 CAAACTCCTGACCTCAAAAATCCTTCTGCGTCAGCCTCTCAGAGTGCTGGGATTACAGCCCATCT CAAACTCCTGACCTCAAAAATCCTTCTGCGTCTGCCTCTCAGAGTGCTGGGATTACAGCCCATCT T A ICE2 Ensembl:ENSG00000128915 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947760420 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1311,RMVar_hsa_circ_60930,RMVar_hsa_circ_300381,RMVar_hsa_circ_328490,RMVar_hsa_circ_57505,RMVar_hsa_circ_8346,RMVar_hsa_circ_17429,RMVar_hsa_circ_172582,RMVar_hsa_circ_378962,RMVar_hsa_circ_68735,RMVar_hsa_circ_273585,RMVar_hsa_circ_350875,RMVar_hsa_circ_73564,RMVar_hsa_circ_73653,RMVar_hsa_circ_172586,RMVar_hsa_circ_301585,RMVar_hsa_circ_61667,RMVar_hsa_circ_343997 38919 RMVar_ID_38919 Human_SNP_ID_579685043 A-to-I Human chr15 - 60489678 60489678 60489678 GGATGGAGACGTCCTCTGCCATAACATGGGCCATAAAGCAAATTCGACATGGGATGTTCTGTTTC GGATGGAGACGTCCTCTGCCATAACATGGGCCGTAAAGCAAATTCGACATGGGATGTTCTGTTTC T C RORA Ensembl:ENSG00000069667 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs748706464 Functional Loss SNV dbSNP153 33..33 33 - - - 38920 RMVar_ID_38920 Human_SNP_ID_579688566 A-to-I Human chr15 - 60504074 60504074 60504074 GATCCAGACCGGGCACGGTGGCTCATCCCTGTAATCCCAGCACTTTGGGAGGCCCAGGCAGACAA GATCCAGACCGGGCACGGTGGCTCATCCCTGTCATCCCAGCACTTTGGGAGGCCCAGGCAGACAA T G RORA Ensembl:ENSG00000069667 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1260098650 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_275923,RMVar_hsa_circ_172587,RMVar_hsa_circ_46427,RMVar_hsa_circ_172589,RMVar_hsa_circ_361570 38921 RMVar_ID_38921 Human_SNP_ID_579688660 A-to-I Human chr15 + 60504453 60504453 60504453 CCGGTACTCCCAGCTACTTGGGAAGCTGAGGCAGAAGAATTACTTGAACCCGGGAGGCGGAGGTT CCGGTACTCCCAGCTACTTGGGAAGCTGAGGCCGAAGAATTACTTGAACCCGGGAGGCGGAGGTT A C RORA-AS1 Ensembl:ENSG00000245534 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs574209288 Functional Loss SNV dbSNP153 33..33 33 - - - 38922 RMVar_ID_38922 Human_SNP_ID_579776746 A-to-I Human chr15 - 60861868 60861868 60861868 GAGTGTAATAGCTGGGATAGAGATCTTAATGAACTTTTAGTGTCATGATGCTTCCAGGACAGAGT GAGTGTAATAGCTGGGATAGAGATCTTAATGATCTTTTAGTGTCATGATGCTTCCAGGACAGAGT T A RORA Ensembl:ENSG00000069667 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1209652544 Functional Loss SNV dbSNP153 33..33 33 - - - 38923 RMVar_ID_38923 Human_SNP_ID_579776989 A-to-I Human chr15 - 60862881 60862881 60862881 AAAAAAGGGCAGTCTTGAAGCATCATGACACTAAAAGCTCATTAAGATCTCTGTCCCAGCTATTA AAAAAAGGGCAGTCTTGAAGCATCATGACACTGAAAGCTCATTAAGATCTCTGTCCCAGCTATTA T C RORA Ensembl:ENSG00000069667 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1236863175 Functional Loss SNV dbSNP153 33..33 33 - - - 38924 RMVar_ID_38924 Human_SNP_ID_579789891 A-to-I Human chr15 - 60912322 60912322 60912322 GAACTCGTGGGCTCAAGCGATCCTGTCATCTCAGCCTCCCAAGTAGCTAGAACGACAGATGCAGC GAACTCGTGGGCTCAAGCGATCCTGTCATCTCGGCCTCCCAAGTAGCTAGAACGACAGATGCAGC T C RORA Ensembl:ENSG00000069667 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1264540124 Functional Loss SNV dbSNP153 33..33 33 - - - 38925 RMVar_ID_38925 Human_SNP_ID_579811669 A-to-I Human chr15 - 60996167 60996167 60996167 GCTTGGGAGTCTGAGGCTGGAGAATCACTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCTGAGAT GCTTGGGAGTCTGAGGCTGGAGAATCACTTGAGCCTGGGAGGCAGAGGTTGCAGTGAGCTGAGAT T C RORA Ensembl:ENSG00000069667 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs575946390 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172592,RMVar_hsa_circ_172591 38926 RMVar_ID_38926 Human_SNP_ID_579828897 A-to-I Human chr15 - 61062032 61062032 61062032 TTGAGACGGAGTCTTGTTCTCTGGCCCAGGCTAGAGTGCAGTGGCACAATCCCAGCTCACTGCAA TTGAGACGGAGTCTTGTTCTCTGGCCCAGGCTTGAGTGCAGTGGCACAATCCCAGCTCACTGCAA T A RORA Ensembl:ENSG00000069667 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs992284444 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172597,RMVar_hsa_circ_172596 38927 RMVar_ID_38927 Human_SNP_ID_579828898 A-to-I Human chr15 - 61062032 61062032 61062032 TTGAGACGGAGTCTTGTTCTCTGGCCCAGGCTAGAGTGCAGTGGCACAATCCCAGCTCACTGCAA TTGAGACGGAGTCTTGTTCTCTGGCCCAGGCTGGAGTGCAGTGGCACAATCCCAGCTCACTGCAA T C RORA Ensembl:ENSG00000069667 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs992284444 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172597,RMVar_hsa_circ_172596 38928 RMVar_ID_38928 Human_SNP_ID_579835993 A-to-I Human chr15 - 61089386 61089386 61089386 TGTATTGTTCATGCAAGAAAAAGCAATGAACAAAGCTACATCTGTGAGAAACAGGATGTTTTCCC TGTATTGTTCATGCAAGAAAAAGCAATGAACAGAGCTACATCTGTGAGAAACAGGATGTTTTCCC T C RORA Ensembl:ENSG00000069667 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs952281693 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172597,RMVar_hsa_circ_172596 38929 RMVar_ID_38929 Human_SNP_ID_579857270 A-to-I Human chr15 - 61173794 61173794 61173794 CAGGCACGGTGGCACAGGCCCCACATGCCTATAGTCCCAGCTACTCGGGAGGCTGAGGTGTGAGG CAGGCACGGTGGCACAGGCCCCACATGCCTATGGTCCCAGCTACTCGGGAGGCTGAGGTGTGAGG T C RORA Ensembl:ENSG00000069667 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1168537580 Functional Loss SNV dbSNP153 33..33 33 - - - 38930 RMVar_ID_38930 Human_SNP_ID_580048991 A-to-I Human chr15 - 61914421 61914421 61914421 AGGATTACAGGTGCCTGCCGCCACACAGTGCTAATTTTTGTATTTTTAGTAGAGATGGGATTTCA AGGATTACAGGTGCCTGCCGCCACACAGTGCTGATTTTTGTATTTTTAGTAGAGATGGGATTTCA T C VPS13C Ensembl:ENSG00000129003 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs879499199 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20033,RMVar_hsa_circ_54041,RMVar_hsa_circ_67621,RMVar_hsa_circ_3516,RMVar_hsa_circ_31753,RMVar_hsa_circ_69556,RMVar_hsa_circ_110835,RMVar_hsa_circ_172613,RMVar_hsa_circ_74444,RMVar_hsa_circ_52455,RMVar_hsa_circ_82186,RMVar_hsa_circ_66537,RMVar_hsa_circ_172616,RMVar_hsa_circ_44958,RMVar_hsa_circ_124064,RMVar_hsa_circ_105713,RMVar_hsa_circ_32681,RMVar_hsa_circ_72923,RMVar_hsa_circ_107089,RMVar_hsa_circ_172618,RMVar_hsa_circ_172619,RMVar_hsa_circ_126243,RMVar_hsa_circ_172622,RMVar_hsa_circ_69140,RMVar_hsa_circ_88815,RMVar_hsa_circ_172623,RMVar_hsa_circ_68872,RMVar_hsa_circ_312089,RMVar_hsa_circ_172621,RMVar_hsa_circ_357718,RMVar_hsa_circ_265616 38931 RMVar_ID_38931 Human_SNP_ID_580187741 A-to-I Human chr15 + 62421992 62421992 62421992 GTGTCAGACTTGCCTATCGGGCCAGGTGCAGTAGCTCACACCTGTAATCCCAGCACTTTGGGAGG GTGTCAGACTTGCCTATCGGGCCAGGTGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGG A G TLN2 Ensembl:ENSG00000171914 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs989888766 Functional Loss SNV dbSNP153 33..33 33 - - - 38932 RMVar_ID_38932 Human_SNP_ID_580367241 A-to-I Human chr15 + 63070294 63070286 63070294 TGACAGCCATGAGTCCTACTTTAAGTATGTATATATATATATATATGTGTGTGTGTGTGTGTGTG TGACAGCCATGAGTCCTACTTTAAG________TATATATATATATGTGTGTGTGTGTGTGTGTG GTATGTATA G TPM1 Ensembl:ENSG00000140416 Protein coding exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1438405929 Functional Loss DEL dbSNP153 26..33 33 - - - RMVar_hsa_circ_172693,RMVar_hsa_circ_115785,RMVar_hsa_circ_76861,RMVar_hsa_circ_172701 38933 RMVar_ID_38933 Human_SNP_ID_580367277 A-to-I Human chr15 + 63070294 63070294 63070294 TGACAGCCATGAGTCCTACTTTAAGTATGTATATATATATATATATGTGTGTGTGTGTGTGTGTG TGACAGCCATGAGTCCTACTTTAAGTATGTATGTATATATATATATGTGTGTGTGTGTGTGTGTG A G TPM1 Ensembl:ENSG00000140416 Protein coding exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs76275714 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172693,RMVar_hsa_circ_115785,RMVar_hsa_circ_76861,RMVar_hsa_circ_172701 38934 RMVar_ID_38934 Human_SNP_ID_580367656 A-to-I Human chr15 + 63071404 63071404 63071404 TTCCCGGGTTGATGCTGCCACACTTTGTAGAGAGTTTAGCAACACAGTGTGCTTAGTCAGCGTAG TTCCCGGGTTGATGCTGCCACACTTTGTAGAGCGTTTAGCAACACAGTGTGCTTAGTCAGCGTAG A C TPM1 Ensembl:ENSG00000140416 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1566977768 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_460440,Human_RBP_ID_5113147,Human_RBP_ID_18161577,Human_RBP_ID_20004056,Human_RBP_ID_22496479,Human_RBP_ID_24474136 RMVar_hsa_circ_172693,RMVar_hsa_circ_115785,RMVar_hsa_circ_76861,RMVar_hsa_circ_172701 38935 RMVar_ID_38935 Human_SNP_ID_580383364 A-to-I Human chr15 + 63128461 63128461 63128461 TCTCCAAAAAAAATTTTAAATTAGCCAGGTTCAGTGGCCTGTGTGTGTAAGTAGTCCTAGCTACT TCTCCAAAAAAAATTTTAAATTAGCCAGGTTCGGTGGCCTGTGTGTGTAAGTAGTCCTAGCTACT A G LACTB Ensembl:ENSG00000103642 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2729823 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26438131 GWAS_ID_4402,GWAS_ID_4403,GWAS_ID_4404,GWAS_ID_4405,GWAS_ID_4406,GWAS_ID_4407,GWAS_ID_4408,GWAS_ID_4409,GWAS_ID_4410,GWAS_ID_4411,GWAS_ID_4412,GWAS_ID_4413,GWAS_ID_4414,GWAS_ID_4415,GWAS_ID_4416,GWAS_ID_4417,GWAS_ID_4418,GWAS_ID_4419,GWAS_ID_4420,GWAS_ID_4421,GWAS_ID_4422,GWAS_ID_4423,GWAS_ID_4424,GWAS_ID_4425,GWAS_ID_4426,GWAS_ID_4427,GWAS_ID_4428,GWAS_ID_4429,GWAS_ID_4430,GWAS_ID_4431,GWAS_ID_4432,GWAS_ID_4433,GWAS_ID_4434,GWAS_ID_4435,GWAS_ID_4436,GWAS_ID_4437,GWAS_ID_4438,GWAS_ID_4439,GWAS_ID_4440,GWAS_ID_4441,GWAS_ID_4442,GWAS_ID_4443,GWAS_ID_4444,GWAS_ID_4445,GWAS_ID_4446,GWAS_ID_4447,GWAS_ID_4448,GWAS_ID_4449,GWAS_ID_4450,GWAS_ID_4451,GWAS_ID_4452,GWAS_ID_4453,GWAS_ID_4454,GWAS_ID_4455,GWAS_ID_4456,GWAS_ID_4457,GWAS_ID_4458,GWAS_ID_4459,GWAS_ID_4460,GWAS_ID_4461 RMVar_hsa_circ_172706,RMVar_hsa_circ_308105 38936 RMVar_ID_38936 Human_SNP_ID_580383371 A-to-I Human chr15 - 63128519 63128519 63128519 ACAACCCACTACAACTTTGAACTCCTGGGCTCAGGGATCCTCCCGCCTCAGCCTCCTGAGTAGCT ACAACCCACTACAACTTTGAACTCCTGGGCTCTGGGATCCTCCCGCCTCAGCCTCCTGAGTAGCT T A RPS27L Ensembl:ENSG00000185088 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910798928 Functional Loss SNV dbSNP153 33..33 33 - - - 38937 RMVar_ID_38937 Human_SNP_ID_580388586 A-to-I Human chr15 - 63150025 63150025 63150025 GTTCCCTAGGTGGAGTGCAGTGGCGTGATCTCAGCTCACTGCAACCTCCTCCACCTCCCAGGCTT GTTCCCTAGGTGGAGTGCAGTGGCGTGATCTCCGCTCACTGCAACCTCCTCCACCTCCCAGGCTT T G RPS27L Ensembl:ENSG00000185088 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1282375104 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_866846,Human_miRNA_ID_1384767 38938 RMVar_ID_38938 Human_SNP_ID_580389051 A-to-I Human chr15 - 63152093 63152093 63152093 TTTGTAGAGATGGGGCTCTGGCTGTGTTGCCCAGGCTGTAAGGAACTCCTGGCCTCAGGTGATCT TTTGTAGAGATGGGGCTCTGGCTGTGTTGCCCGGGCTGTAAGGAACTCCTGGCCTCAGGTGATCT T C RPS27L Ensembl:ENSG00000185088 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs930955853 Functional Loss SNV dbSNP153 33..33 33 - - - 38939 RMVar_ID_38939 Human_SNP_ID_580389087 A-to-I Human chr15 - 63152196 63152196 63152196 TAGCTCATTGTGACCTCAAACTCCTGGGCTCAAGCAAGCCTCCCACCTCTGCCTCCTGAGTAGCG TAGCTCATTGTGACCTCAAACTCCTGGGCTCATGCAAGCCTCCCACCTCTGCCTCCTGAGTAGCG T A RPS27L Ensembl:ENSG00000185088 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs959302384 Functional Loss SNV dbSNP153 33..33 33 - - - 38940 RMVar_ID_38940 Human_SNP_ID_580389469 A-to-I Human chr15 - 63153642 63153642 63153642 CGGCTCACTGCAACCTCCGCCTCCCAGGTCCAAGCAATTCTCTTGCCTTGTCCTCCCAAGTAGCT CGGCTCACTGCAACCTCCGCCTCCCAGGTCCAGGCAATTCTCTTGCCTTGTCCTCCCAAGTAGCT T C RPS27L Ensembl:ENSG00000185088 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006974497 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_460482 38941 RMVar_ID_38941 Human_SNP_ID_580414967 A-to-I Human chr15 + 63258201 63258201 63258201 TTGGCTCACTACAACCTCTGGCTCCCTGGTTCAAGCGATTCTCCTGTCTCAGCCTCCCAAGTAGC TTGGCTCACTACAACCTCTGGCTCCCTGGTTCGAGCGATTCTCCTGTCTCAGCCTCCCAAGTAGC A G RAB8B Ensembl:ENSG00000166128 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1219997575 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172711,RMVar_hsa_circ_78004,RMVar_hsa_circ_332152,RMVar_hsa_circ_172712,RMVar_hsa_circ_103442,RMVar_hsa_circ_330287,RMVar_hsa_circ_172716,RMVar_hsa_circ_172717,RMVar_hsa_circ_172718,RMVar_hsa_circ_318256 38942 RMVar_ID_38942 Human_SNP_ID_580426203 A-to-I Human chr15 + 63304277 63304277 63304277 TGGTCACCCTCAGTGGGGGCAGGGACTGGTGGAACAGGGAGGCTCCTGGGGGCTGAGAATGTTTT TGGTCACCCTCAGTGGGGGCAGGGACTGGTGGGACAGGGAGGCTCCTGGGGGCTGAGAATGTTTT A G APH1B Ensembl:ENSG00000138613 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903959199 Functional Loss SNV dbSNP153 33..33 33 - - - 38943 RMVar_ID_38943 Human_SNP_ID_580486987 A-to-I Human chr15 + 63548773 63548772 63548773 CCTAGTGGAGTGGCATGATCTCTGCTCACTGCAACCTCTGTCTCCCGGGTTCAGGCAATTCTCAT CCTAGTGGAGTGGCATGATCTCTGCTCACTGC_ACCTCTGTCTCCCGGGTTCAGGCAATTCTCAT CA C USP3 Ensembl:ENSG00000140455 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1422555631 Functional Loss DEL dbSNP153 33..33 33 - - - 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 38944 RMVar_ID_38944 Human_SNP_ID_580495111 A-to-I Human chr15 + 63581913 63581912 63581914 CACCCTTTTGCCCAGGCTGGTCTTGAATTCCTAGGCTCAAATGATCCTCCACCTCAGCCTCCCAA CACCCTTTTGCCCAGGCTGGTCTTGAATTCCT__GCTCAAATGATCCTCCACCTCAGCCTCCCAA TAG T USP3 Ensembl:ENSG00000140455 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1288709592 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_345614,RMVar_hsa_circ_106362,RMVar_hsa_circ_97277,RMVar_hsa_circ_172726,RMVar_hsa_circ_172727,RMVar_hsa_circ_172725,RMVar_hsa_circ_114761,RMVar_hsa_circ_172734,RMVar_hsa_circ_39768,RMVar_hsa_circ_172749,RMVar_hsa_circ_54706 38945 RMVar_ID_38945 Human_SNP_ID_580495112 A-to-I Human chr15 + 63581913 63581913 63581913 CACCCTTTTGCCCAGGCTGGTCTTGAATTCCTAGGCTCAAATGATCCTCCACCTCAGCCTCCCAA CACCCTTTTGCCCAGGCTGGTCTTGAATTCCTGGGCTCAAATGATCCTCCACCTCAGCCTCCCAA A G USP3 Ensembl:ENSG00000140455 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs568699394 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_345614,RMVar_hsa_circ_106362,RMVar_hsa_circ_97277,RMVar_hsa_circ_172726,RMVar_hsa_circ_172727,RMVar_hsa_circ_172725,RMVar_hsa_circ_114761,RMVar_hsa_circ_172734,RMVar_hsa_circ_39768,RMVar_hsa_circ_172749,RMVar_hsa_circ_54706 38946 RMVar_ID_38946 Human_SNP_ID_580501049 A-to-I Human chr15 + 63602571 63602568 63602572 ATCGTGCCACTGCACTCCAGCCTGGGCGACAGAGAGACTCTTGTCTCAAAAAAAAAAAAAAAAAA ATCGTGCCACTGCACTCCAGCCTGGGCGAC____AGACTCTTGTCTCAAAAAAAAAAAAAAAAAA CAGAG C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1391566866 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_22388164 38947 RMVar_ID_38947 Human_SNP_ID_580514321 A-to-I Human chr15 - 63652839 63652839 63652839 TCGAGACCAGCCTGGCCATCATGGCGAAACCTATCTCTACTAAAAATACAAAAATTATCCAGTTG TCGAGACCAGCCTGGCCATCATGGCGAAACCTGTCTCTACTAAAAATACAAAAATTATCCAGTTG T C HERC1 Ensembl:ENSG00000103657 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1055814511 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106342,RMVar_hsa_circ_8066,RMVar_hsa_circ_172760,RMVar_hsa_circ_75838,RMVar_hsa_circ_107075,RMVar_hsa_circ_172761,RMVar_hsa_circ_80615,RMVar_hsa_circ_98090,RMVar_hsa_circ_82636,RMVar_hsa_circ_21538,RMVar_hsa_circ_76853,RMVar_hsa_circ_13983,RMVar_hsa_circ_116410,RMVar_hsa_circ_172763,RMVar_hsa_circ_172765,RMVar_hsa_circ_172766,RMVar_hsa_circ_172764,RMVar_hsa_circ_276341,RMVar_hsa_circ_120139,RMVar_hsa_circ_172770,RMVar_hsa_circ_127620,RMVar_hsa_circ_119811,RMVar_hsa_circ_107203,RMVar_hsa_circ_106483,RMVar_hsa_circ_172781,RMVar_hsa_circ_85143,RMVar_hsa_circ_102580,RMVar_hsa_circ_105441,RMVar_hsa_circ_100684,RMVar_hsa_circ_78701,RMVar_hsa_circ_83431,RMVar_hsa_circ_13701,RMVar_hsa_circ_58560,RMVar_hsa_circ_172782,RMVar_hsa_circ_172773,RMVar_hsa_circ_172777,RMVar_hsa_circ_172779,RMVar_hsa_circ_172780,RMVar_hsa_circ_172778,RMVar_hsa_circ_172775,RMVar_hsa_circ_172776,RMVar_hsa_circ_172774,RMVar_hsa_circ_92278,RMVar_hsa_circ_172771,RMVar_hsa_circ_172772,RMVar_hsa_circ_111005,RMVar_hsa_circ_112755,RMVar_hsa_circ_172792,RMVar_hsa_circ_172793,RMVar_hsa_circ_266391,RMVar_hsa_circ_172795,RMVar_hsa_circ_84599,RMVar_hsa_circ_172794,RMVar_hsa_circ_52663,RMVar_hsa_circ_53393,RMVar_hsa_circ_103060,RMVar_hsa_circ_26838,RMVar_hsa_circ_172801,RMVar_hsa_circ_172802,RMVar_hsa_circ_90514,RMVar_hsa_circ_80877,RMVar_hsa_circ_172803,RMVar_hsa_circ_172804,RMVar_hsa_circ_125000,RMVar_hsa_circ_17643,RMVar_hsa_circ_63417,RMVar_hsa_circ_102535,RMVar_hsa_circ_172806,RMVar_hsa_circ_172807,RMVar_hsa_circ_119436,RMVar_hsa_circ_172809,RMVar_hsa_circ_172808,RMVar_hsa_circ_96771,RMVar_hsa_circ_266844,RMVar_hsa_circ_298468,RMVar_hsa_circ_111141,RMVar_hsa_circ_91224,RMVar_hsa_circ_35395,RMVar_hsa_circ_19724,RMVar_hsa_circ_70157,RMVar_hsa_circ_172810,RMVar_hsa_circ_172812,RMVar_hsa_circ_172813,RMVar_hsa_circ_172814,RMVar_hsa_circ_172811,RMVar_hsa_circ_90703,RMVar_hsa_circ_93601,RMVar_hsa_circ_105880,RMVar_hsa_circ_172815,RMVar_hsa_circ_172816,RMVar_hsa_circ_89458,RMVar_hsa_circ_20470,RMVar_hsa_circ_172819,RMVar_hsa_circ_104934,RMVar_hsa_circ_172817,RMVar_hsa_circ_172818,RMVar_hsa_circ_108660,RMVar_hsa_circ_172820,RMVar_hsa_circ_107424,RMVar_hsa_circ_330582,RMVar_hsa_circ_343895,RMVar_hsa_circ_110306,RMVar_hsa_circ_172821,RMVar_hsa_circ_37435,RMVar_hsa_circ_172822,RMVar_hsa_circ_116286,RMVar_hsa_circ_100256,RMVar_hsa_circ_110291,RMVar_hsa_circ_340421,RMVar_hsa_circ_172823,RMVar_hsa_circ_267040,RMVar_hsa_circ_105909,RMVar_hsa_circ_95632,RMVar_hsa_circ_172825,RMVar_hsa_circ_172827,RMVar_hsa_circ_78175,RMVar_hsa_circ_172826,RMVar_hsa_circ_172824,RMVar_hsa_circ_35477,RMVar_hsa_circ_172828,RMVar_hsa_circ_75871,RMVar_hsa_circ_84655,RMVar_hsa_circ_172829,RMVar_hsa_circ_109882,RMVar_hsa_circ_313200,RMVar_hsa_circ_371340,RMVar_hsa_circ_172830,RMVar_hsa_circ_368598,RMVar_hsa_circ_121094,RMVar_hsa_circ_22792,RMVar_hsa_circ_52213,RMVar_hsa_circ_172832,RMVar_hsa_circ_172833,RMVar_hsa_circ_306543,RMVar_hsa_circ_172834,RMVar_hsa_circ_172835 38948 RMVar_ID_38948 Human_SNP_ID_580514322 A-to-I Human chr15 - 63652839 63652839 63652839 TCGAGACCAGCCTGGCCATCATGGCGAAACCTATCTCTACTAAAAATACAAAAATTATCCAGTTG TCGAGACCAGCCTGGCCATCATGGCGAAACCTCTCTCTACTAAAAATACAAAAATTATCCAGTTG T G HERC1 Ensembl:ENSG00000103657 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1055814511 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106342,RMVar_hsa_circ_8066,RMVar_hsa_circ_172760,RMVar_hsa_circ_75838,RMVar_hsa_circ_107075,RMVar_hsa_circ_172761,RMVar_hsa_circ_80615,RMVar_hsa_circ_98090,RMVar_hsa_circ_82636,RMVar_hsa_circ_21538,RMVar_hsa_circ_76853,RMVar_hsa_circ_13983,RMVar_hsa_circ_116410,RMVar_hsa_circ_172763,RMVar_hsa_circ_172765,RMVar_hsa_circ_172766,RMVar_hsa_circ_172764,RMVar_hsa_circ_276341,RMVar_hsa_circ_120139,RMVar_hsa_circ_172770,RMVar_hsa_circ_127620,RMVar_hsa_circ_119811,RMVar_hsa_circ_107203,RMVar_hsa_circ_106483,RMVar_hsa_circ_172781,RMVar_hsa_circ_85143,RMVar_hsa_circ_102580,RMVar_hsa_circ_105441,RMVar_hsa_circ_100684,RMVar_hsa_circ_78701,RMVar_hsa_circ_83431,RMVar_hsa_circ_13701,RMVar_hsa_circ_58560,RMVar_hsa_circ_172782,RMVar_hsa_circ_172773,RMVar_hsa_circ_172777,RMVar_hsa_circ_172779,RMVar_hsa_circ_172780,RMVar_hsa_circ_172778,RMVar_hsa_circ_172775,RMVar_hsa_circ_172776,RMVar_hsa_circ_172774,RMVar_hsa_circ_92278,RMVar_hsa_circ_172771,RMVar_hsa_circ_172772,RMVar_hsa_circ_111005,RMVar_hsa_circ_112755,RMVar_hsa_circ_172792,RMVar_hsa_circ_172793,RMVar_hsa_circ_266391,RMVar_hsa_circ_172795,RMVar_hsa_circ_84599,RMVar_hsa_circ_172794,RMVar_hsa_circ_52663,RMVar_hsa_circ_53393,RMVar_hsa_circ_103060,RMVar_hsa_circ_26838,RMVar_hsa_circ_172801,RMVar_hsa_circ_172802,RMVar_hsa_circ_90514,RMVar_hsa_circ_80877,RMVar_hsa_circ_172803,RMVar_hsa_circ_172804,RMVar_hsa_circ_125000,RMVar_hsa_circ_17643,RMVar_hsa_circ_63417,RMVar_hsa_circ_102535,RMVar_hsa_circ_172806,RMVar_hsa_circ_172807,RMVar_hsa_circ_119436,RMVar_hsa_circ_172809,RMVar_hsa_circ_172808,RMVar_hsa_circ_96771,RMVar_hsa_circ_266844,RMVar_hsa_circ_298468,RMVar_hsa_circ_111141,RMVar_hsa_circ_91224,RMVar_hsa_circ_35395,RMVar_hsa_circ_19724,RMVar_hsa_circ_70157,RMVar_hsa_circ_172810,RMVar_hsa_circ_172812,RMVar_hsa_circ_172813,RMVar_hsa_circ_172814,RMVar_hsa_circ_172811,RMVar_hsa_circ_90703,RMVar_hsa_circ_93601,RMVar_hsa_circ_105880,RMVar_hsa_circ_172815,RMVar_hsa_circ_172816,RMVar_hsa_circ_89458,RMVar_hsa_circ_20470,RMVar_hsa_circ_172819,RMVar_hsa_circ_104934,RMVar_hsa_circ_172817,RMVar_hsa_circ_172818,RMVar_hsa_circ_108660,RMVar_hsa_circ_172820,RMVar_hsa_circ_107424,RMVar_hsa_circ_330582,RMVar_hsa_circ_343895,RMVar_hsa_circ_110306,RMVar_hsa_circ_172821,RMVar_hsa_circ_37435,RMVar_hsa_circ_172822,RMVar_hsa_circ_116286,RMVar_hsa_circ_100256,RMVar_hsa_circ_110291,RMVar_hsa_circ_340421,RMVar_hsa_circ_172823,RMVar_hsa_circ_267040,RMVar_hsa_circ_105909,RMVar_hsa_circ_95632,RMVar_hsa_circ_172825,RMVar_hsa_circ_172827,RMVar_hsa_circ_78175,RMVar_hsa_circ_172826,RMVar_hsa_circ_172824,RMVar_hsa_circ_35477,RMVar_hsa_circ_172828,RMVar_hsa_circ_75871,RMVar_hsa_circ_84655,RMVar_hsa_circ_172829,RMVar_hsa_circ_109882,RMVar_hsa_circ_313200,RMVar_hsa_circ_371340,RMVar_hsa_circ_172830,RMVar_hsa_circ_368598,RMVar_hsa_circ_121094,RMVar_hsa_circ_22792,RMVar_hsa_circ_52213,RMVar_hsa_circ_172832,RMVar_hsa_circ_172833,RMVar_hsa_circ_306543,RMVar_hsa_circ_172834,RMVar_hsa_circ_172835 38949 RMVar_ID_38949 Human_SNP_ID_580514420 A-to-I Human chr15 - 63653284 63653284 63653284 TGTACACCACCACACTCGGCTAATTTTTTTGTATTTTTAGTGGAGACAGGGTTTTTCCATGTTGG TGTACACCACCACACTCGGCTAATTTTTTTGTGTTTTTAGTGGAGACAGGGTTTTTCCATGTTGG T C HERC1 Ensembl:ENSG00000103657 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1358157760 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106342,RMVar_hsa_circ_8066,RMVar_hsa_circ_172760,RMVar_hsa_circ_75838,RMVar_hsa_circ_107075,RMVar_hsa_circ_172761,RMVar_hsa_circ_80615,RMVar_hsa_circ_98090,RMVar_hsa_circ_82636,RMVar_hsa_circ_21538,RMVar_hsa_circ_76853,RMVar_hsa_circ_13983,RMVar_hsa_circ_116410,RMVar_hsa_circ_172763,RMVar_hsa_circ_172765,RMVar_hsa_circ_172766,RMVar_hsa_circ_172764,RMVar_hsa_circ_276341,RMVar_hsa_circ_120139,RMVar_hsa_circ_172770,RMVar_hsa_circ_127620,RMVar_hsa_circ_119811,RMVar_hsa_circ_107203,RMVar_hsa_circ_106483,RMVar_hsa_circ_172781,RMVar_hsa_circ_85143,RMVar_hsa_circ_102580,RMVar_hsa_circ_105441,RMVar_hsa_circ_100684,RMVar_hsa_circ_78701,RMVar_hsa_circ_83431,RMVar_hsa_circ_13701,RMVar_hsa_circ_58560,RMVar_hsa_circ_172782,RMVar_hsa_circ_172773,RMVar_hsa_circ_172777,RMVar_hsa_circ_172779,RMVar_hsa_circ_172780,RMVar_hsa_circ_172778,RMVar_hsa_circ_172775,RMVar_hsa_circ_172776,RMVar_hsa_circ_172774,RMVar_hsa_circ_92278,RMVar_hsa_circ_172771,RMVar_hsa_circ_172772,RMVar_hsa_circ_111005,RMVar_hsa_circ_112755,RMVar_hsa_circ_172792,RMVar_hsa_circ_172793,RMVar_hsa_circ_266391,RMVar_hsa_circ_172795,RMVar_hsa_circ_84599,RMVar_hsa_circ_172794,RMVar_hsa_circ_52663,RMVar_hsa_circ_53393,RMVar_hsa_circ_103060,RMVar_hsa_circ_26838,RMVar_hsa_circ_172801,RMVar_hsa_circ_172802,RMVar_hsa_circ_90514,RMVar_hsa_circ_80877,RMVar_hsa_circ_172803,RMVar_hsa_circ_172804,RMVar_hsa_circ_125000,RMVar_hsa_circ_17643,RMVar_hsa_circ_63417,RMVar_hsa_circ_102535,RMVar_hsa_circ_172806,RMVar_hsa_circ_172807,RMVar_hsa_circ_119436,RMVar_hsa_circ_172809,RMVar_hsa_circ_172808,RMVar_hsa_circ_96771,RMVar_hsa_circ_266844,RMVar_hsa_circ_298468,RMVar_hsa_circ_111141,RMVar_hsa_circ_91224,RMVar_hsa_circ_35395,RMVar_hsa_circ_19724,RMVar_hsa_circ_70157,RMVar_hsa_circ_172810,RMVar_hsa_circ_172812,RMVar_hsa_circ_172813,RMVar_hsa_circ_172814,RMVar_hsa_circ_172811,RMVar_hsa_circ_90703,RMVar_hsa_circ_93601,RMVar_hsa_circ_105880,RMVar_hsa_circ_172815,RMVar_hsa_circ_172816,RMVar_hsa_circ_89458,RMVar_hsa_circ_20470,RMVar_hsa_circ_172819,RMVar_hsa_circ_104934,RMVar_hsa_circ_172817,RMVar_hsa_circ_172818,RMVar_hsa_circ_108660,RMVar_hsa_circ_172820,RMVar_hsa_circ_107424,RMVar_hsa_circ_330582,RMVar_hsa_circ_343895,RMVar_hsa_circ_110306,RMVar_hsa_circ_172821,RMVar_hsa_circ_37435,RMVar_hsa_circ_172822,RMVar_hsa_circ_116286,RMVar_hsa_circ_100256,RMVar_hsa_circ_110291,RMVar_hsa_circ_340421,RMVar_hsa_circ_172823,RMVar_hsa_circ_267040,RMVar_hsa_circ_105909,RMVar_hsa_circ_95632,RMVar_hsa_circ_172825,RMVar_hsa_circ_172827,RMVar_hsa_circ_78175,RMVar_hsa_circ_172826,RMVar_hsa_circ_172824,RMVar_hsa_circ_35477,RMVar_hsa_circ_172828,RMVar_hsa_circ_75871,RMVar_hsa_circ_84655,RMVar_hsa_circ_172829,RMVar_hsa_circ_109882,RMVar_hsa_circ_313200,RMVar_hsa_circ_371340,RMVar_hsa_circ_172830,RMVar_hsa_circ_368598,RMVar_hsa_circ_121094,RMVar_hsa_circ_22792,RMVar_hsa_circ_52213,RMVar_hsa_circ_172832,RMVar_hsa_circ_172833,RMVar_hsa_circ_306543,RMVar_hsa_circ_172834,RMVar_hsa_circ_172835 38950 RMVar_ID_38950 Human_SNP_ID_580524663 A-to-I Human chr15 - 63693304 63693304 63693304 GGGAGGTGGAGATTGCAGTGAGCTGAGATCACACCACTGCACTTTAGCCTGGATGACAGAGCGAG GGGAGGTGGAGATTGCAGTGAGCTGAGATCACGCCACTGCACTTTAGCCTGGATGACAGAGCGAG T C HERC1 Ensembl:ENSG00000103657 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1004481649 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25151255 RMVar_hsa_circ_98090,RMVar_hsa_circ_13983,RMVar_hsa_circ_116410,RMVar_hsa_circ_172763,RMVar_hsa_circ_127620,RMVar_hsa_circ_107203,RMVar_hsa_circ_105441,RMVar_hsa_circ_78701,RMVar_hsa_circ_83431,RMVar_hsa_circ_172773,RMVar_hsa_circ_172775,RMVar_hsa_circ_172776,RMVar_hsa_circ_172774,RMVar_hsa_circ_172771,RMVar_hsa_circ_172772,RMVar_hsa_circ_111005,RMVar_hsa_circ_172792,RMVar_hsa_circ_172795,RMVar_hsa_circ_84599,RMVar_hsa_circ_19178,RMVar_hsa_circ_103060,RMVar_hsa_circ_172801,RMVar_hsa_circ_90514,RMVar_hsa_circ_172804,RMVar_hsa_circ_17643,RMVar_hsa_circ_119436,RMVar_hsa_circ_172809,RMVar_hsa_circ_96771,RMVar_hsa_circ_298468,RMVar_hsa_circ_111141,RMVar_hsa_circ_91224,RMVar_hsa_circ_172810,RMVar_hsa_circ_172812,RMVar_hsa_circ_172813,RMVar_hsa_circ_172811,RMVar_hsa_circ_89458,RMVar_hsa_circ_172819,RMVar_hsa_circ_104934,RMVar_hsa_circ_172818,RMVar_hsa_circ_108660,RMVar_hsa_circ_172820,RMVar_hsa_circ_107424,RMVar_hsa_circ_172822,RMVar_hsa_circ_100256,RMVar_hsa_circ_95632,RMVar_hsa_circ_172827,RMVar_hsa_circ_172828,RMVar_hsa_circ_84655,RMVar_hsa_circ_109882,RMVar_hsa_circ_172830,RMVar_hsa_circ_121094,RMVar_hsa_circ_22792,RMVar_hsa_circ_172832,RMVar_hsa_circ_172833,RMVar_hsa_circ_107188,RMVar_hsa_circ_172837,RMVar_hsa_circ_302336,RMVar_hsa_circ_172843,RMVar_hsa_circ_172845,RMVar_hsa_circ_91002,RMVar_hsa_circ_95139,RMVar_hsa_circ_172844,RMVar_hsa_circ_87208,RMVar_hsa_circ_172846,RMVar_hsa_circ_322248,RMVar_hsa_circ_98561,RMVar_hsa_circ_30842,RMVar_hsa_circ_57352,RMVar_hsa_circ_89469,RMVar_hsa_circ_108315,RMVar_hsa_circ_121773,RMVar_hsa_circ_172848,RMVar_hsa_circ_172847,RMVar_hsa_circ_124210,RMVar_hsa_circ_118238,RMVar_hsa_circ_115779,RMVar_hsa_circ_94034,RMVar_hsa_circ_90475,RMVar_hsa_circ_172856,RMVar_hsa_circ_172860,RMVar_hsa_circ_172864,RMVar_hsa_circ_84618,RMVar_hsa_circ_88167,RMVar_hsa_circ_79446,RMVar_hsa_circ_172862,RMVar_hsa_circ_172863,RMVar_hsa_circ_172861,RMVar_hsa_circ_172858,RMVar_hsa_circ_172859,RMVar_hsa_circ_172857,RMVar_hsa_circ_172854,RMVar_hsa_circ_172855,RMVar_hsa_circ_99644,RMVar_hsa_circ_172873,RMVar_hsa_circ_93016,RMVar_hsa_circ_102307,RMVar_hsa_circ_122617,RMVar_hsa_circ_99411,RMVar_hsa_circ_76460,RMVar_hsa_circ_20543,RMVar_hsa_circ_71951,RMVar_hsa_circ_172875,RMVar_hsa_circ_172877,RMVar_hsa_circ_172879,RMVar_hsa_circ_172878,RMVar_hsa_circ_172876,RMVar_hsa_circ_33289,RMVar_hsa_circ_62463,RMVar_hsa_circ_91578,RMVar_hsa_circ_377054,RMVar_hsa_circ_77710,RMVar_hsa_circ_97492,RMVar_hsa_circ_123385,RMVar_hsa_circ_172885,RMVar_hsa_circ_172886,RMVar_hsa_circ_172884,RMVar_hsa_circ_121540,RMVar_hsa_circ_122168,RMVar_hsa_circ_104534,RMVar_hsa_circ_89101,RMVar_hsa_circ_96677,RMVar_hsa_circ_79518,RMVar_hsa_circ_28064,RMVar_hsa_circ_121330,RMVar_hsa_circ_172893,RMVar_hsa_circ_172895,RMVar_hsa_circ_172897,RMVar_hsa_circ_172896,RMVar_hsa_circ_172894,RMVar_hsa_circ_172891,RMVar_hsa_circ_172892,RMVar_hsa_circ_172890,RMVar_hsa_circ_365734,RMVar_hsa_circ_119910,RMVar_hsa_circ_120279,RMVar_hsa_circ_116052,RMVar_hsa_circ_103214,RMVar_hsa_circ_104726,RMVar_hsa_circ_106695,RMVar_hsa_circ_104588,RMVar_hsa_circ_97129,RMVar_hsa_circ_99192,RMVar_hsa_circ_95384,RMVar_hsa_circ_172905,RMVar_hsa_circ_172913,RMVar_hsa_circ_82065,RMVar_hsa_circ_87579,RMVar_hsa_circ_89841,RMVar_hsa_circ_82563,RMVar_hsa_circ_80242,RMVar_hsa_circ_172915,RMVar_hsa_circ_172916,RMVar_hsa_circ_172914,RMVar_hsa_circ_172909,RMVar_hsa_circ_172911,RMVar_hsa_circ_172912,RMVar_hsa_circ_172910,RMVar_hsa_circ_172907,RMVar_hsa_circ_172908,RMVar_hsa_circ_172906,RMVar_hsa_circ_172901,RMVar_hsa_circ_172903,RMVar_hsa_circ_172904,RMVar_hsa_circ_172902,RMVar_hsa_circ_305961,RMVar_hsa_circ_114153,RMVar_hsa_circ_172920,RMVar_hsa_circ_312728,RMVar_hsa_circ_55264,RMVar_hsa_circ_31607,RMVar_hsa_circ_14588,RMVar_hsa_circ_79225,RMVar_hsa_circ_172922,RMVar_hsa_circ_172923,RMVar_hsa_circ_172921,RMVar_hsa_circ_308694,RMVar_hsa_circ_25955,RMVar_hsa_circ_172926,RMVar_hsa_circ_172927,RMVar_hsa_circ_297933,RMVar_hsa_circ_345566,RMVar_hsa_circ_300111,RMVar_hsa_circ_45961,RMVar_hsa_circ_172929,RMVar_hsa_circ_172931,RMVar_hsa_circ_16725,RMVar_hsa_circ_172930,RMVar_hsa_circ_172928 38951 RMVar_ID_38951 Human_SNP_ID_580524690 A-to-I Human chr15 - 63693400 63693400 63693400 ATCTCTACTAAAAATATGAAAATTAGCCTGGCATGGTGACGCATGCCTGTAGTGCCAGCTGCTTG ATCTCTACTAAAAATATGAAAATTAGCCTGGCGTGGTGACGCATGCCTGTAGTGCCAGCTGCTTG T C HERC1 Ensembl:ENSG00000103657 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs767503197 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98090,RMVar_hsa_circ_13983,RMVar_hsa_circ_116410,RMVar_hsa_circ_172763,RMVar_hsa_circ_127620,RMVar_hsa_circ_107203,RMVar_hsa_circ_105441,RMVar_hsa_circ_78701,RMVar_hsa_circ_83431,RMVar_hsa_circ_172773,RMVar_hsa_circ_172775,RMVar_hsa_circ_172776,RMVar_hsa_circ_172774,RMVar_hsa_circ_172771,RMVar_hsa_circ_172772,RMVar_hsa_circ_111005,RMVar_hsa_circ_172792,RMVar_hsa_circ_172795,RMVar_hsa_circ_84599,RMVar_hsa_circ_19178,RMVar_hsa_circ_103060,RMVar_hsa_circ_172801,RMVar_hsa_circ_90514,RMVar_hsa_circ_172804,RMVar_hsa_circ_17643,RMVar_hsa_circ_119436,RMVar_hsa_circ_172809,RMVar_hsa_circ_96771,RMVar_hsa_circ_298468,RMVar_hsa_circ_111141,RMVar_hsa_circ_91224,RMVar_hsa_circ_172810,RMVar_hsa_circ_172812,RMVar_hsa_circ_172813,RMVar_hsa_circ_172811,RMVar_hsa_circ_89458,RMVar_hsa_circ_172819,RMVar_hsa_circ_104934,RMVar_hsa_circ_172818,RMVar_hsa_circ_108660,RMVar_hsa_circ_172820,RMVar_hsa_circ_107424,RMVar_hsa_circ_172822,RMVar_hsa_circ_100256,RMVar_hsa_circ_95632,RMVar_hsa_circ_172827,RMVar_hsa_circ_172828,RMVar_hsa_circ_84655,RMVar_hsa_circ_109882,RMVar_hsa_circ_172830,RMVar_hsa_circ_121094,RMVar_hsa_circ_22792,RMVar_hsa_circ_172832,RMVar_hsa_circ_172833,RMVar_hsa_circ_107188,RMVar_hsa_circ_172837,RMVar_hsa_circ_302336,RMVar_hsa_circ_172843,RMVar_hsa_circ_172845,RMVar_hsa_circ_91002,RMVar_hsa_circ_95139,RMVar_hsa_circ_172844,RMVar_hsa_circ_87208,RMVar_hsa_circ_172846,RMVar_hsa_circ_322248,RMVar_hsa_circ_98561,RMVar_hsa_circ_30842,RMVar_hsa_circ_57352,RMVar_hsa_circ_89469,RMVar_hsa_circ_108315,RMVar_hsa_circ_121773,RMVar_hsa_circ_172848,RMVar_hsa_circ_172847,RMVar_hsa_circ_124210,RMVar_hsa_circ_118238,RMVar_hsa_circ_115779,RMVar_hsa_circ_94034,RMVar_hsa_circ_90475,RMVar_hsa_circ_172856,RMVar_hsa_circ_172860,RMVar_hsa_circ_172864,RMVar_hsa_circ_84618,RMVar_hsa_circ_88167,RMVar_hsa_circ_79446,RMVar_hsa_circ_172862,RMVar_hsa_circ_172863,RMVar_hsa_circ_172861,RMVar_hsa_circ_172858,RMVar_hsa_circ_172859,RMVar_hsa_circ_172857,RMVar_hsa_circ_172854,RMVar_hsa_circ_172855,RMVar_hsa_circ_99644,RMVar_hsa_circ_172873,RMVar_hsa_circ_93016,RMVar_hsa_circ_102307,RMVar_hsa_circ_122617,RMVar_hsa_circ_99411,RMVar_hsa_circ_76460,RMVar_hsa_circ_20543,RMVar_hsa_circ_71951,RMVar_hsa_circ_172875,RMVar_hsa_circ_172877,RMVar_hsa_circ_172879,RMVar_hsa_circ_172878,RMVar_hsa_circ_172876,RMVar_hsa_circ_33289,RMVar_hsa_circ_62463,RMVar_hsa_circ_91578,RMVar_hsa_circ_377054,RMVar_hsa_circ_77710,RMVar_hsa_circ_97492,RMVar_hsa_circ_123385,RMVar_hsa_circ_172885,RMVar_hsa_circ_172886,RMVar_hsa_circ_172884,RMVar_hsa_circ_121540,RMVar_hsa_circ_122168,RMVar_hsa_circ_104534,RMVar_hsa_circ_89101,RMVar_hsa_circ_96677,RMVar_hsa_circ_79518,RMVar_hsa_circ_28064,RMVar_hsa_circ_121330,RMVar_hsa_circ_172893,RMVar_hsa_circ_172895,RMVar_hsa_circ_172897,RMVar_hsa_circ_172896,RMVar_hsa_circ_172894,RMVar_hsa_circ_172891,RMVar_hsa_circ_172892,RMVar_hsa_circ_172890,RMVar_hsa_circ_365734,RMVar_hsa_circ_119910,RMVar_hsa_circ_120279,RMVar_hsa_circ_116052,RMVar_hsa_circ_103214,RMVar_hsa_circ_104726,RMVar_hsa_circ_106695,RMVar_hsa_circ_104588,RMVar_hsa_circ_97129,RMVar_hsa_circ_99192,RMVar_hsa_circ_95384,RMVar_hsa_circ_172905,RMVar_hsa_circ_172913,RMVar_hsa_circ_82065,RMVar_hsa_circ_87579,RMVar_hsa_circ_89841,RMVar_hsa_circ_82563,RMVar_hsa_circ_80242,RMVar_hsa_circ_172915,RMVar_hsa_circ_172916,RMVar_hsa_circ_172914,RMVar_hsa_circ_172909,RMVar_hsa_circ_172911,RMVar_hsa_circ_172912,RMVar_hsa_circ_172910,RMVar_hsa_circ_172907,RMVar_hsa_circ_172908,RMVar_hsa_circ_172906,RMVar_hsa_circ_172901,RMVar_hsa_circ_172903,RMVar_hsa_circ_172904,RMVar_hsa_circ_172902,RMVar_hsa_circ_305961,RMVar_hsa_circ_114153,RMVar_hsa_circ_172920,RMVar_hsa_circ_312728,RMVar_hsa_circ_55264,RMVar_hsa_circ_31607,RMVar_hsa_circ_14588,RMVar_hsa_circ_79225,RMVar_hsa_circ_172922,RMVar_hsa_circ_172923,RMVar_hsa_circ_172921,RMVar_hsa_circ_308694,RMVar_hsa_circ_25955,RMVar_hsa_circ_172926,RMVar_hsa_circ_172927,RMVar_hsa_circ_297933,RMVar_hsa_circ_345566,RMVar_hsa_circ_300111,RMVar_hsa_circ_45961,RMVar_hsa_circ_172929,RMVar_hsa_circ_172931,RMVar_hsa_circ_16725,RMVar_hsa_circ_172930,RMVar_hsa_circ_172928 38952 RMVar_ID_38952 Human_SNP_ID_580524699 A-to-I Human chr15 - 63693432 63693432 63693432 CAAGATCAGCCTGGGCAACATGGTGGAACCCCATCTCTACTAAAAATATGAAAATTAGCCTGGCA CAAGATCAGCCTGGGCAACATGGTGGAACCCCGTCTCTACTAAAAATATGAAAATTAGCCTGGCA T C HERC1 Ensembl:ENSG00000103657 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1275396182 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98090,RMVar_hsa_circ_13983,RMVar_hsa_circ_116410,RMVar_hsa_circ_172763,RMVar_hsa_circ_127620,RMVar_hsa_circ_107203,RMVar_hsa_circ_105441,RMVar_hsa_circ_78701,RMVar_hsa_circ_83431,RMVar_hsa_circ_172773,RMVar_hsa_circ_172775,RMVar_hsa_circ_172776,RMVar_hsa_circ_172774,RMVar_hsa_circ_172771,RMVar_hsa_circ_172772,RMVar_hsa_circ_111005,RMVar_hsa_circ_172792,RMVar_hsa_circ_172795,RMVar_hsa_circ_84599,RMVar_hsa_circ_19178,RMVar_hsa_circ_103060,RMVar_hsa_circ_172801,RMVar_hsa_circ_90514,RMVar_hsa_circ_172804,RMVar_hsa_circ_17643,RMVar_hsa_circ_119436,RMVar_hsa_circ_172809,RMVar_hsa_circ_96771,RMVar_hsa_circ_298468,RMVar_hsa_circ_111141,RMVar_hsa_circ_91224,RMVar_hsa_circ_172810,RMVar_hsa_circ_172812,RMVar_hsa_circ_172813,RMVar_hsa_circ_172811,RMVar_hsa_circ_89458,RMVar_hsa_circ_172819,RMVar_hsa_circ_104934,RMVar_hsa_circ_172818,RMVar_hsa_circ_108660,RMVar_hsa_circ_172820,RMVar_hsa_circ_107424,RMVar_hsa_circ_172822,RMVar_hsa_circ_100256,RMVar_hsa_circ_95632,RMVar_hsa_circ_172827,RMVar_hsa_circ_172828,RMVar_hsa_circ_84655,RMVar_hsa_circ_109882,RMVar_hsa_circ_172830,RMVar_hsa_circ_121094,RMVar_hsa_circ_22792,RMVar_hsa_circ_172832,RMVar_hsa_circ_172833,RMVar_hsa_circ_107188,RMVar_hsa_circ_172837,RMVar_hsa_circ_302336,RMVar_hsa_circ_172843,RMVar_hsa_circ_172845,RMVar_hsa_circ_91002,RMVar_hsa_circ_95139,RMVar_hsa_circ_172844,RMVar_hsa_circ_87208,RMVar_hsa_circ_172846,RMVar_hsa_circ_322248,RMVar_hsa_circ_98561,RMVar_hsa_circ_30842,RMVar_hsa_circ_57352,RMVar_hsa_circ_89469,RMVar_hsa_circ_108315,RMVar_hsa_circ_121773,RMVar_hsa_circ_172848,RMVar_hsa_circ_172847,RMVar_hsa_circ_124210,RMVar_hsa_circ_118238,RMVar_hsa_circ_115779,RMVar_hsa_circ_94034,RMVar_hsa_circ_90475,RMVar_hsa_circ_172856,RMVar_hsa_circ_172860,RMVar_hsa_circ_172864,RMVar_hsa_circ_84618,RMVar_hsa_circ_88167,RMVar_hsa_circ_79446,RMVar_hsa_circ_172862,RMVar_hsa_circ_172863,RMVar_hsa_circ_172861,RMVar_hsa_circ_172858,RMVar_hsa_circ_172859,RMVar_hsa_circ_172857,RMVar_hsa_circ_172854,RMVar_hsa_circ_172855,RMVar_hsa_circ_99644,RMVar_hsa_circ_172873,RMVar_hsa_circ_93016,RMVar_hsa_circ_102307,RMVar_hsa_circ_122617,RMVar_hsa_circ_99411,RMVar_hsa_circ_76460,RMVar_hsa_circ_20543,RMVar_hsa_circ_71951,RMVar_hsa_circ_172875,RMVar_hsa_circ_172877,RMVar_hsa_circ_172879,RMVar_hsa_circ_172878,RMVar_hsa_circ_172876,RMVar_hsa_circ_33289,RMVar_hsa_circ_62463,RMVar_hsa_circ_91578,RMVar_hsa_circ_377054,RMVar_hsa_circ_77710,RMVar_hsa_circ_97492,RMVar_hsa_circ_123385,RMVar_hsa_circ_172885,RMVar_hsa_circ_172886,RMVar_hsa_circ_172884,RMVar_hsa_circ_121540,RMVar_hsa_circ_122168,RMVar_hsa_circ_104534,RMVar_hsa_circ_89101,RMVar_hsa_circ_96677,RMVar_hsa_circ_79518,RMVar_hsa_circ_28064,RMVar_hsa_circ_121330,RMVar_hsa_circ_172893,RMVar_hsa_circ_172895,RMVar_hsa_circ_172897,RMVar_hsa_circ_172896,RMVar_hsa_circ_172894,RMVar_hsa_circ_172891,RMVar_hsa_circ_172892,RMVar_hsa_circ_172890,RMVar_hsa_circ_365734,RMVar_hsa_circ_119910,RMVar_hsa_circ_120279,RMVar_hsa_circ_116052,RMVar_hsa_circ_103214,RMVar_hsa_circ_104726,RMVar_hsa_circ_106695,RMVar_hsa_circ_104588,RMVar_hsa_circ_97129,RMVar_hsa_circ_99192,RMVar_hsa_circ_95384,RMVar_hsa_circ_172905,RMVar_hsa_circ_172913,RMVar_hsa_circ_82065,RMVar_hsa_circ_87579,RMVar_hsa_circ_89841,RMVar_hsa_circ_82563,RMVar_hsa_circ_80242,RMVar_hsa_circ_172915,RMVar_hsa_circ_172916,RMVar_hsa_circ_172914,RMVar_hsa_circ_172909,RMVar_hsa_circ_172911,RMVar_hsa_circ_172912,RMVar_hsa_circ_172910,RMVar_hsa_circ_172907,RMVar_hsa_circ_172908,RMVar_hsa_circ_172906,RMVar_hsa_circ_172901,RMVar_hsa_circ_172903,RMVar_hsa_circ_172904,RMVar_hsa_circ_172902,RMVar_hsa_circ_305961,RMVar_hsa_circ_114153,RMVar_hsa_circ_172920,RMVar_hsa_circ_312728,RMVar_hsa_circ_55264,RMVar_hsa_circ_31607,RMVar_hsa_circ_14588,RMVar_hsa_circ_79225,RMVar_hsa_circ_172922,RMVar_hsa_circ_172923,RMVar_hsa_circ_172921,RMVar_hsa_circ_308694,RMVar_hsa_circ_25955,RMVar_hsa_circ_172926,RMVar_hsa_circ_172927,RMVar_hsa_circ_297933,RMVar_hsa_circ_345566,RMVar_hsa_circ_300111,RMVar_hsa_circ_45961,RMVar_hsa_circ_172929,RMVar_hsa_circ_172931,RMVar_hsa_circ_16725,RMVar_hsa_circ_172930,RMVar_hsa_circ_172928 38953 RMVar_ID_38953 Human_SNP_ID_580536781 A-to-I Human chr15 - 63739781 63739781 63739781 CAAGCTGGAGTGCAGTGGCTCGATCTCGGCTCACTGTAACCTCCACGTCCTGGGTTCAAGCGATT CAAGCTGGAGTGCAGTGGCTCGATCTCGGCTCCCTGTAACCTCCACGTCCTGGGTTCAAGCGATT T G HERC1 Ensembl:ENSG00000103657 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1278467855 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172795,RMVar_hsa_circ_84599,RMVar_hsa_circ_90514,RMVar_hsa_circ_172804,RMVar_hsa_circ_119436,RMVar_hsa_circ_172809,RMVar_hsa_circ_111141,RMVar_hsa_circ_172810,RMVar_hsa_circ_89458,RMVar_hsa_circ_172819,RMVar_hsa_circ_104934,RMVar_hsa_circ_172818,RMVar_hsa_circ_108660,RMVar_hsa_circ_172820,RMVar_hsa_circ_100256,RMVar_hsa_circ_172827,RMVar_hsa_circ_109882,RMVar_hsa_circ_172830,RMVar_hsa_circ_121094,RMVar_hsa_circ_172833,RMVar_hsa_circ_107188,RMVar_hsa_circ_172837,RMVar_hsa_circ_95139,RMVar_hsa_circ_172844,RMVar_hsa_circ_98561,RMVar_hsa_circ_30842,RMVar_hsa_circ_57352,RMVar_hsa_circ_108315,RMVar_hsa_circ_121773,RMVar_hsa_circ_172847,RMVar_hsa_circ_124210,RMVar_hsa_circ_115779,RMVar_hsa_circ_172856,RMVar_hsa_circ_88167,RMVar_hsa_circ_172858,RMVar_hsa_circ_172857,RMVar_hsa_circ_172854,RMVar_hsa_circ_172855,RMVar_hsa_circ_99644,RMVar_hsa_circ_172873,RMVar_hsa_circ_102307,RMVar_hsa_circ_76460,RMVar_hsa_circ_172875,RMVar_hsa_circ_172876,RMVar_hsa_circ_33289,RMVar_hsa_circ_377054,RMVar_hsa_circ_172884,RMVar_hsa_circ_89101,RMVar_hsa_circ_96677,RMVar_hsa_circ_79518,RMVar_hsa_circ_172891,RMVar_hsa_circ_172892,RMVar_hsa_circ_172890,RMVar_hsa_circ_116052,RMVar_hsa_circ_104726,RMVar_hsa_circ_106695,RMVar_hsa_circ_99192,RMVar_hsa_circ_95384,RMVar_hsa_circ_172905,RMVar_hsa_circ_89841,RMVar_hsa_circ_82563,RMVar_hsa_circ_80242,RMVar_hsa_circ_172907,RMVar_hsa_circ_172908,RMVar_hsa_circ_172906,RMVar_hsa_circ_172901,RMVar_hsa_circ_172903,RMVar_hsa_circ_172904,RMVar_hsa_circ_172902,RMVar_hsa_circ_114153,RMVar_hsa_circ_172920,RMVar_hsa_circ_31607,RMVar_hsa_circ_6021,RMVar_hsa_circ_345566,RMVar_hsa_circ_172931,RMVar_hsa_circ_125257,RMVar_hsa_circ_13457,RMVar_hsa_circ_172934,RMVar_hsa_circ_297676,RMVar_hsa_circ_351879,RMVar_hsa_circ_357289,RMVar_hsa_circ_12528,RMVar_hsa_circ_172936,RMVar_hsa_circ_172935,RMVar_hsa_circ_371346,RMVar_hsa_circ_376981,RMVar_hsa_circ_172946,RMVar_hsa_circ_367637,RMVar_hsa_circ_377106,RMVar_hsa_circ_172953,RMVar_hsa_circ_22494,RMVar_hsa_circ_66446,RMVar_hsa_circ_301981,RMVar_hsa_circ_15607,RMVar_hsa_circ_172956,RMVar_hsa_circ_304767,RMVar_hsa_circ_172958,RMVar_hsa_circ_54750,RMVar_hsa_circ_308412,RMVar_hsa_circ_378379,RMVar_hsa_circ_329174,RMVar_hsa_circ_282165,RMVar_hsa_circ_99481,RMVar_hsa_circ_172960,RMVar_hsa_circ_172961,RMVar_hsa_circ_172959,RMVar_hsa_circ_172971,RMVar_hsa_circ_18214,RMVar_hsa_circ_50786,RMVar_hsa_circ_294237,RMVar_hsa_circ_312298,RMVar_hsa_circ_172962,RMVar_hsa_circ_319792,RMVar_hsa_circ_172966,RMVar_hsa_circ_34087,RMVar_hsa_circ_172965,RMVar_hsa_circ_327196,RMVar_hsa_circ_373178,RMVar_hsa_circ_52502,RMVar_hsa_circ_172968,RMVar_hsa_circ_172969,RMVar_hsa_circ_377743,RMVar_hsa_circ_338249,RMVar_hsa_circ_273366,RMVar_hsa_circ_172973,RMVar_hsa_circ_31697,RMVar_hsa_circ_172972,RMVar_hsa_circ_172975,RMVar_hsa_circ_172970,RMVar_hsa_circ_325572 38954 RMVar_ID_38954 Human_SNP_ID_580548994 A-to-I Human chr15 - 63787798 63787798 63787798 ACCACGCCCGGTTAATTTTTTGTATTATTTGTAGAGTCGGGGTTTTGCCATATTGTCCAGGTTAG ACCACGCCCGGTTAATTTTTTGTATTATTTGTGGAGTCGGGGTTTTGCCATATTGTCCAGGTTAG T C HERC1 Ensembl:ENSG00000103657 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1298340793 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115779,RMVar_hsa_circ_172854,RMVar_hsa_circ_104726,RMVar_hsa_circ_172901 38955 RMVar_ID_38955 Human_SNP_ID_580559516 A-to-I Human chr15 - 63829371 63829371 63829371 TCACCCAGGCTGCAGTGCCGTGGCGTGATCATAGCTTACTGCAGCCTTGAACTCCTGGGCTTAAG TCACCCAGGCTGCAGTGCCGTGGCGTGATCATGGCTTACTGCAGCCTTGAACTCCTGGGCTTAAG T C HERC1 Ensembl:ENSG00000103657 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1338088763 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115779,RMVar_hsa_circ_172854,RMVar_hsa_circ_104726,RMVar_hsa_circ_172901 38956 RMVar_ID_38956 Human_SNP_ID_580621393 A-to-I Human chr15 - 64076981 64076981 64076981 AAAATTGGGGCCAGGTGCAGTGGCTCACGCCTATAATCTCTGTACTTTGGGAGGCCTAGATGGGC AAAATTGGGGCCAGGTGCAGTGGCTCACGCCTGTAATCTCTGTACTTTGGGAGGCCTAGATGGGC T C CIAO2A Ensembl:ENSG00000166797 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1428829339 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25151476 RMVar_hsa_circ_115904,RMVar_hsa_circ_111139,RMVar_hsa_circ_172996,RMVar_hsa_circ_172997,RMVar_hsa_circ_57185,RMVar_hsa_circ_310827,RMVar_hsa_circ_172998 38957 RMVar_ID_38957 Human_SNP_ID_580621747 A-to-I Human chr15 - 64078469 64078469 64078469 ACCACACCCAGCTAAATTTTTGTATTTTTAGTAGAGACAGGGTTTTGCCATGTTGGCCAGTTTGG ACCACACCCAGCTAAATTTTTGTATTTTTAGTGGAGACAGGGTTTTGCCATGTTGGCCAGTTTGG T C CIAO2A Ensembl:ENSG00000166797 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1237643031 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115904,RMVar_hsa_circ_111139,RMVar_hsa_circ_172996,RMVar_hsa_circ_172997,RMVar_hsa_circ_57185,RMVar_hsa_circ_310827,RMVar_hsa_circ_172998 38958 RMVar_ID_38958 Human_SNP_ID_580621882 A-to-I Human chr15 - 64078786 64078786 64078786 TCCCGCCTTGGTTTCCCAAAGTGTTTCGGATTACAGGCGTGAGCCACTGCACCCAGCCCCGTGGC TCCCGCCTTGGTTTCCCAAAGTGTTTCGGATTGCAGGCGTGAGCCACTGCACCCAGCCCCGTGGC T C CIAO2A Ensembl:ENSG00000166797 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1302067221 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12549946 RMVar_hsa_circ_115904,RMVar_hsa_circ_111139,RMVar_hsa_circ_172996,RMVar_hsa_circ_172997,RMVar_hsa_circ_57185,RMVar_hsa_circ_310827,RMVar_hsa_circ_172998 38959 RMVar_ID_38959 Human_SNP_ID_580621989 A-to-I Human chr15 - 64079205 64079205 64079205 GCCCAGTGAAATACTATTTTATTTTCCATGATATCAGTCCTGATTTCTTTCTTCTTTTTAAGATG GCCCAGTGAAATACTATTTTATTTTCCATGATTTCAGTCCTGATTTCTTTCTTCTTTTTAAGATG T A CIAO2A Ensembl:ENSG00000166797 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs371515 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12549956 RMVar_hsa_circ_115904,RMVar_hsa_circ_111139,RMVar_hsa_circ_172996,RMVar_hsa_circ_172997,RMVar_hsa_circ_57185,RMVar_hsa_circ_310827,RMVar_hsa_circ_172998 38960 RMVar_ID_38960 Human_SNP_ID_580621990 A-to-I Human chr15 - 64079205 64079205 64079205 GCCCAGTGAAATACTATTTTATTTTCCATGATATCAGTCCTGATTTCTTTCTTCTTTTTAAGATG GCCCAGTGAAATACTATTTTATTTTCCATGATGTCAGTCCTGATTTCTTTCTTCTTTTTAAGATG T C CIAO2A Ensembl:ENSG00000166797 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs371515 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12549956 RMVar_hsa_circ_115904,RMVar_hsa_circ_111139,RMVar_hsa_circ_172996,RMVar_hsa_circ_172997,RMVar_hsa_circ_57185,RMVar_hsa_circ_310827,RMVar_hsa_circ_172998 38961 RMVar_ID_38961 Human_SNP_ID_580623281 A-to-I Human chr15 - 64084607 64084607 64084607 GCACCACCACACCTGGCTAATTTTGTATTTTTAATAGAGATGTGGTTTCTCTATGTTGGTCAGGC GCACCACCACACCTGGCTAATTTTGTATTTTTCATAGAGATGTGGTTTCTCTATGTTGGTCAGGC T G CIAO2A Ensembl:ENSG00000166797 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs958821860 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111139,RMVar_hsa_circ_74127,RMVar_hsa_circ_172997,RMVar_hsa_circ_310827,RMVar_hsa_circ_172998 38962 RMVar_ID_38962 Human_SNP_ID_580623290 A-to-I Human chr15 - 64084647 64084647 64084647 CTCCTGCCTCAGCCTCCCAAGCAGCTGGGATTACAGACATGCACCACCACACCTGGCTAATTTTG CTCCTGCCTCAGCCTCCCAAGCAGCTGGGATTGCAGACATGCACCACCACACCTGGCTAATTTTG T C CIAO2A Ensembl:ENSG00000166797 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1388007390 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111139,RMVar_hsa_circ_74127,RMVar_hsa_circ_172997,RMVar_hsa_circ_310827,RMVar_hsa_circ_172998 38963 RMVar_ID_38963 Human_SNP_ID_580623500 A-to-I Human chr15 - 64085382 64085382 64085382 GTGATCCTCCCACCTCAGTCTCCTGAAAAGTTAGAACTTCAGGCAGGTGCCACTATGCCTGGCTA GTGATCCTCCCACCTCAGTCTCCTGAAAAGTTGGAACTTCAGGCAGGTGCCACTATGCCTGGCTA T C CIAO2A Ensembl:ENSG00000166797 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs952761054 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111139,RMVar_hsa_circ_74127,RMVar_hsa_circ_172997,RMVar_hsa_circ_310827,RMVar_hsa_circ_172998 38964 RMVar_ID_38964 Human_SNP_ID_580627440 A-to-I Human chr15 + 64099791 64099791 64099791 TGGAGTGCAGTGGCACAATCTCAGCTCACTGCAGCCCCTGCCTCCTGGGTTCAAGCGATTCTCCT TGGAGTGCAGTGGCACAATCTCAGCTCACTGCCGCCCCTGCCTCCTGGGTTCAAGCGATTCTCCT A C SNX1 Ensembl:ENSG00000028528 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs967946767 Functional Loss SNV dbSNP153 33..33 33 - - - 38965 RMVar_ID_38965 Human_SNP_ID_580628066 A-to-I Human chr15 + 64102317 64102317 64102317 ACATATTTTTAGGATACACATGGTATTTTGATATCTGTATACAAAGTGTGATGACCAAATCAAGG ACATATTTTTAGGATACACATGGTATTTTGATGTCTGTATACAAAGTGTGATGACCAAATCAAGG A G SNX1 Ensembl:ENSG00000028528 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1477140442 Functional Loss SNV dbSNP153 33..33 33 - - - 38966 RMVar_ID_38966 Human_SNP_ID_580628694 A-to-I Human chr15 + 64104683 64104683 64104683 AAGGCAGGTAGATCACCTGAGGTTGGGAGTTCAAGACCAGCCTGGCCAACATAGTGAAACCCCAT AAGGCAGGTAGATCACCTGAGGTTGGGAGTTCGAGACCAGCCTGGCCAACATAGTGAAACCCCAT A G SNX1 Ensembl:ENSG00000028528 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1336613974 Functional Loss SNV dbSNP153 33..33 33 - - - 38967 RMVar_ID_38967 Human_SNP_ID_580632312 A-to-I Human chr15 + 64119257 64119257 64119257 CCTCCCGCCTGAGCCACCCCAGCCGCCCAAGTAGCTGGGACTGCAGGCACGTGCTACCATGCCGA CCTCCCGCCTGAGCCACCCCAGCCGCCCAAGTGGCTGGGACTGCAGGCACGTGCTACCATGCCGA A G SNX1 Ensembl:ENSG00000028528 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270948003 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37303,RMVar_hsa_circ_317414,RMVar_hsa_circ_333973,RMVar_hsa_circ_329055,RMVar_hsa_circ_289077,RMVar_hsa_circ_289565,RMVar_hsa_circ_126785,RMVar_hsa_circ_172999,RMVar_hsa_circ_173001,RMVar_hsa_circ_173002,RMVar_hsa_circ_173000,RMVar_hsa_circ_173006,RMVar_hsa_circ_278963,RMVar_hsa_circ_65786,RMVar_hsa_circ_26235,RMVar_hsa_circ_104553,RMVar_hsa_circ_173007,RMVar_hsa_circ_173008 38968 RMVar_ID_38968 Human_SNP_ID_580632750 A-to-I Human chr15 + 64120774 64120774 64120774 GAGGTGGGAGGATCATTTGAGCCTGGAAGGTCAAGGCTGCAGTGAGCTGAGGTAATACTACTGCA GAGGTGGGAGGATCATTTGAGCCTGGAAGGTCCAGGCTGCAGTGAGCTGAGGTAATACTACTGCA A C SNX1 Ensembl:ENSG00000028528 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1163116028 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37303,RMVar_hsa_circ_317414,RMVar_hsa_circ_333973,RMVar_hsa_circ_329055,RMVar_hsa_circ_289077,RMVar_hsa_circ_289565,RMVar_hsa_circ_126785,RMVar_hsa_circ_172999,RMVar_hsa_circ_173001,RMVar_hsa_circ_173002,RMVar_hsa_circ_173000,RMVar_hsa_circ_173006,RMVar_hsa_circ_278963,RMVar_hsa_circ_65786,RMVar_hsa_circ_26235,RMVar_hsa_circ_104553,RMVar_hsa_circ_173007,RMVar_hsa_circ_173008 38969 RMVar_ID_38969 Human_SNP_ID_580638310 A-to-I Human chr15 + 64142129 64142129 64142129 GGGAGGCCGAGGTGGGAGAATCACTTGAGCCCAAGAATTTGAGACCAGCCTGGGGAATATAGTGA GGGAGGCCGAGGTGGGAGAATCACTTGAGCCCCAGAATTTGAGACCAGCCTGGGGAATATAGTGA A C SNX1 Ensembl:ENSG00000028528 Protein coding 3'UTR GSE38233;GSE99789 cultured B-cells;esophageal squamous carcinoma cells,EC109 - 24183664,29796672 RNA-Seq:(High) rs1485035662 Functional Loss SNV dbSNP153 33..33 33 - - - 38970 RMVar_ID_38970 Human_SNP_ID_580638317 A-to-I Human chr15 + 64142157 64142157 64142157 GCCCAAGAATTTGAGACCAGCCTGGGGAATATAGTGAGACCCTGTCCCTACAAAAATAAAAACAA GCCCAAGAATTTGAGACCAGCCTGGGGAATATGGTGAGACCCTGTCCCTACAAAAATAAAAACAA A G SNX1 Ensembl:ENSG00000028528 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs779908531 Functional Loss SNV dbSNP153 33..33 33 - - - 38971 RMVar_ID_38971 Human_SNP_ID_580638319 A-to-I Human chr15 + 64142174 64142174 64142174 CAGCCTGGGGAATATAGTGAGACCCTGTCCCTACAAAAATAAAAACAACTAGCTGGGTGTGTGGT CAGCCTGGGGAATATAGTGAGACCCTGTCCCTTCAAAAATAAAAACAACTAGCTGGGTGTGTGGT A T SNX1 Ensembl:ENSG00000028528 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1176364883 Functional Loss SNV dbSNP153 33..33 33 - - - 38972 RMVar_ID_38972 Human_SNP_ID_580638348 A-to-I Human chr15 + 64142303 64142303 64142303 TGAGCTACAGTTGCGCCACTGCACTCCAGCCTAGGTGACAGAGCAAGATCTTGTCTCAAAAAAAA TGAGCTACAGTTGCGCCACTGCACTCCAGCCTGGGTGACAGAGCAAGATCTTGTCTCAAAAAAAA A G SNX1 Ensembl:ENSG00000028528 Protein coding 3'UTR GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1007825792 Functional Loss SNV dbSNP153 33..33 33 - - - 38973 RMVar_ID_38973 Human_SNP_ID_580641930 A-to-I Human chr15 + 64154804 64154804 64154804 TCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGATGGGTGGATCACCTGAAGTCAGGAGTTCG TCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGATGGGTGGATCACCTGAAGTCAGGAGTTCG A G SNX22 Ensembl:ENSG00000157734 Protein coding exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs896912943 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1612785 38974 RMVar_ID_38974 Human_SNP_ID_580641935 A-to-I Human chr15 + 64154818 64154818 64154818 CCAGCACTTTGGGAGGCCAAGATGGGTGGATCACCTGAAGTCAGGAGTTCGAGACCAGCCTGACC CCAGCACTTTGGGAGGCCAAGATGGGTGGATCCCCTGAAGTCAGGAGTTCGAGACCAGCCTGACC A C SNX22 Ensembl:ENSG00000157734 Protein coding exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs993639712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1612785 38975 RMVar_ID_38975 Human_SNP_ID_580642039 A-to-I Human chr15 + 64155007 64155007 64155007 TTTTTTGAGACGGAGTTTCACTCTTGTTGCCCAGGCTGGAATGCAATGGCACGATCTCGGCTCAC TTTTTTGAGACGGAGTTTCACTCTTGTTGCCCGGGCTGGAATGCAATGGCACGATCTCGGCTCAC A G SNX22 Ensembl:ENSG00000157734 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1456628873 Functional Loss SNV dbSNP153 33..33 33 - - - 38976 RMVar_ID_38976 Human_SNP_ID_580642041 A-to-I Human chr15 + 64155019 64155019 64155019 GAGTTTCACTCTTGTTGCCCAGGCTGGAATGCAATGGCACGATCTCGGCTCACGGCAACCCCCGC GAGTTTCACTCTTGTTGCCCAGGCTGGAATGCGATGGCACGATCTCGGCTCACGGCAACCCCCGC A G SNX22 Ensembl:ENSG00000157734 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1178733512 Functional Loss SNV dbSNP153 33..33 33 - - - 38977 RMVar_ID_38977 Human_SNP_ID_580642095 A-to-I Human chr15 + 64155202 64155202 64155202 CCAGGCTGGTCTTGTACTCCTGACGTCAGGTGATCCACCCGCCTCGGCTTCCCAAAGTGCTGGGA CCAGGCTGGTCTTGTACTCCTGACGTCAGGTGGTCCACCCGCCTCGGCTTCCCAAAGTGCTGGGA A G SNX22 Ensembl:ENSG00000157734 Protein coding exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1209224671 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1612786 38978 RMVar_ID_38978 Human_SNP_ID_580642103 A-to-I Human chr15 + 64155223 64155223 64155223 GACGTCAGGTGATCCACCCGCCTCGGCTTCCCAAAGTGCTGGGATTACGGGCGTGAGCCACCGTG GACGTCAGGTGATCCACCCGCCTCGGCTTCCCCAAGTGCTGGGATTACGGGCGTGAGCCACCGTG A C SNX22 Ensembl:ENSG00000157734 Protein coding exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1227742111 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23161893 38979 RMVar_ID_38979 Human_SNP_ID_580642126 A-to-I Human chr15 + 64155269 64155269 64155269 ACGGGCGTGAGCCACCGTGCTCGGCCCAAGGCAGGAGAATCTCTTGAAGCCAGGAGGCGGAAGTT ACGGGCGTGAGCCACCGTGCTCGGCCCAAGGCGGGAGAATCTCTTGAAGCCAGGAGGCGGAAGTT A G SNX22 Ensembl:ENSG00000157734 Protein coding exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1235056259 Functional Loss SNV dbSNP153 33..33 33 - - - 38980 RMVar_ID_38980 Human_SNP_ID_580642130 A-to-I Human chr15 + 64155288 64155288 64155288 CTCGGCCCAAGGCAGGAGAATCTCTTGAAGCCAGGAGGCGGAAGTTGTGGTGAGCCGAGATCGCG CTCGGCCCAAGGCAGGAGAATCTCTTGAAGCCGGGAGGCGGAAGTTGTGGTGAGCCGAGATCGCG A G SNX22 Ensembl:ENSG00000157734 Protein coding exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1039182148 Functional Loss SNV dbSNP153 33..33 33 - - - 38981 RMVar_ID_38981 Human_SNP_ID_580642180 A-to-I Human chr15 + 64155492 64155492 64155492 GTCTGGAAGTTTGAGACCAGCCAGCGCAACATAGTGAGACCTGTCTCTACCAAAAAAAAAAAAAA GTCTGGAAGTTTGAGACCAGCCAGCGCAACATGGTGAGACCTGTCTCTACCAAAAAAAAAAAAAA A G SNX22 Ensembl:ENSG00000157734 Protein coding exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1325317752 Functional Loss SNV dbSNP153 33..33 33 - - - 38982 RMVar_ID_38982 Human_SNP_ID_580643645 A-to-I Human chr15 - 64160922 64160922 64160922 AAACAGGCTGGGCATGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCGGAGGAGGGCAGA AAACAGGCTGGGCATGGTGGCTCACACCTGTAGTCCCAGCACTTTGGGAGGCGGAGGAGGGCAGA T C PPIB Ensembl:ENSG00000166794 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1351735248 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_320972,RMVar_hsa_circ_266058 38983 RMVar_ID_38983 Human_SNP_ID_580643794 A-to-I Human chr15 - 64161423 64161423 64161423 CTATGCCCGGCCAAAAAAAATTTTTTTTAATTAGCTGGGTGTGACGGGGTGCACCTGTGGTCCCA CTATGCCCGGCCAAAAAAAATTTTTTTTAATTGGCTGGGTGTGACGGGGTGCACCTGTGGTCCCA T C PPIB Ensembl:ENSG00000166794 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1376487907 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12550933 RMVar_hsa_circ_320972,RMVar_hsa_circ_266058 38984 RMVar_ID_38984 Human_SNP_ID_580645169 A-to-I Human chr15 - 64165994 64165994 64165994 GAAATTTGTAGTATTTTTAAACATGAATGTCAATTTCAAGTGTATTTGAAATGGTTCCTCCAGGA GAAATTTGTAGTATTTTTAAACATGAATGTCAGTTTCAAGTGTATTTGAAATGGTTCCTCCAGGA T C CSNK1G1 Ensembl:ENSG00000169118 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs368506081 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1831644,Human_RBP_ID_18280820 Human_Splice_Rec_1612886,Human_Splice_Rec_1612906 Human_miRNA_ID_1531950 RMVar_hsa_circ_173017,RMVar_hsa_circ_119743 38985 RMVar_ID_38985 Human_SNP_ID_580645172 A-to-I Human chr15 - 64166000 64166000 64166000 GAAAATGAAATTTGTAGTATTTTTAAACATGAATGTCAATTTCAAGTGTATTTGAAATGGTTCCT GAAAATGAAATTTGTAGTATTTTTAAACATGAGTGTCAATTTCAAGTGTATTTGAAATGGTTCCT T C CSNK1G1 Ensembl:ENSG00000169118 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs767343722 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1831644,Human_RBP_ID_18280820 Human_Splice_Rec_1612886,Human_Splice_Rec_1612906 Human_miRNA_ID_391976,Human_miRNA_ID_397995,Human_miRNA_ID_404046,Human_miRNA_ID_410023,Human_miRNA_ID_1249348,Human_miRNA_ID_1411344,Human_miRNA_ID_2120310,Human_miRNA_ID_2123526,Human_miRNA_ID_2126745,Human_miRNA_ID_2129965,Human_miRNA_ID_2602589 RMVar_hsa_circ_173017,RMVar_hsa_circ_119743 38986 RMVar_ID_38986 Human_SNP_ID_580648227 A-to-I Human chr15 - 64179163 64179163 64179163 TGGCTAACTGCAGCCTCTATTCCCCAAGCTCAAGTGATCCTCCTGCCTCAGTCTCCCAAAGTCAT TGGCTAACTGCAGCCTCTATTCCCCAAGCTCAGGTGATCCTCCTGCCTCAGTCTCCCAAAGTCAT T C CSNK1G1 Ensembl:ENSG00000169118 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs771410606 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_173017,RMVar_hsa_circ_119743 38987 RMVar_ID_38987 Human_SNP_ID_580653734 A-to-I Human chr15 - 64201186 64201186 64201186 ATTACCTCAACCTCTGTCTCCCAGATTCAAGCAATTCTCCTGTCTCAGCCTCCCAAGTAGCTGGG ATTACCTCAACCTCTGTCTCCCAGATTCAAGCGATTCTCCTGTCTCAGCCTCCCAAGTAGCTGGG T C CSNK1G1,AC087632.2 Ensembl:ENSG00000169118,Ensembl:ENSG00000259316 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1040489288 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25924,RMVar_hsa_circ_30031,RMVar_hsa_circ_310451,RMVar_hsa_circ_345240,RMVar_hsa_circ_341296,RMVar_hsa_circ_173020,RMVar_hsa_circ_173022,RMVar_hsa_circ_27840,RMVar_hsa_circ_173021,RMVar_hsa_circ_352291,RMVar_hsa_circ_173019,RMVar_hsa_circ_359679,RMVar_hsa_circ_330987,RMVar_hsa_circ_173023,RMVar_hsa_circ_173024 38988 RMVar_ID_38988 Human_SNP_ID_580659915 A-to-I Human chr15 - 64226546 64226546 64226546 TTTGTTTGTTTGTTTGTTTGTTTTGAGACGGAATCTTGCTCTGTCACTGGGCTGGAGTACAGTGT TTTGTTTGTTTGTTTGTTTGTTTTGAGACGGAGTCTTGCTCTGTCACTGGGCTGGAGTACAGTGT T C CSNK1G1,AC087632.2 Ensembl:ENSG00000169118,Ensembl:ENSG00000259316 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049674470 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_30031,RMVar_hsa_circ_173022,RMVar_hsa_circ_273744,RMVar_hsa_circ_280056,RMVar_hsa_circ_359307,RMVar_hsa_circ_38423,RMVar_hsa_circ_26714,RMVar_hsa_circ_376536,RMVar_hsa_circ_358926 38989 RMVar_ID_38989 Human_SNP_ID_580684146 A-to-I Human chr15 - 64322711 64322711 64322711 ATCCCACTTCAGCCTCCTGAGTAGCTGGGACTACAGATGCGCACTACCATGTCTGGCTAATTTTT ATCCCACTTCAGCCTCCTGAGTAGCTGGGACTGCAGATGCGCACTACCATGTCTGGCTAATTTTT T C CSNK1G1,AC087632.2 Ensembl:ENSG00000169118,Ensembl:ENSG00000259316 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs937482896 Functional Loss SNV dbSNP153 33..33 33 - - - 38990 RMVar_ID_38990 Human_SNP_ID_580693957 A-to-I Human chr15 - 64361447 64361447 64361447 AGAATTGCTTGAGTCCAGGTGGTTGAGGCTGCAGTGAGTCATGATCACATCACTGCACTCTAACC AGAATTGCTTGAGTCCAGGTGGTTGAGGCTGCTGTGAGTCATGATCACATCACTGCACTCTAACC T A AC087632.2 Ensembl:ENSG00000259316 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1047475675 Functional Loss SNV dbSNP153 33..33 33 - - - 38991 RMVar_ID_38991 Human_SNP_ID_580693958 A-to-I Human chr15 - 64361447 64361447 64361447 AGAATTGCTTGAGTCCAGGTGGTTGAGGCTGCAGTGAGTCATGATCACATCACTGCACTCTAACC AGAATTGCTTGAGTCCAGGTGGTTGAGGCTGCGGTGAGTCATGATCACATCACTGCACTCTAACC T C AC087632.2 Ensembl:ENSG00000259316 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1047475675 Functional Loss SNV dbSNP153 33..33 33 - - - 38992 RMVar_ID_38992 Human_SNP_ID_580693962 A-to-I Human chr15 - 64361463 64361463 64361463 TGTAGGCTGAGGTGGTAGAATTGCTTGAGTCCAGGTGGTTGAGGCTGCAGTGAGTCATGATCACA TGTAGGCTGAGGTGGTAGAATTGCTTGAGTCCGGGTGGTTGAGGCTGCAGTGAGTCATGATCACA T C AC087632.2 Ensembl:ENSG00000259316 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1257088540 Functional Loss SNV dbSNP153 33..33 33 - - - 38993 RMVar_ID_38993 Human_SNP_ID_580693968 A-to-I Human chr15 - 64361499 64361499 64361499 GGGCATGGTGGCTCACATCTGTGGTCCCGGCTACTTTGTAGGCTGAGGTGGTAGAATTGCTTGAG GGGCATGGTGGCTCACATCTGTGGTCCCGGCTGCTTTGTAGGCTGAGGTGGTAGAATTGCTTGAG T C AC087632.2 Ensembl:ENSG00000259316 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1228603035 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17863859 38994 RMVar_ID_38994 Human_SNP_ID_580693981 A-to-I Human chr15 - 64361535 64361535 64361535 TAGACCTCATCTCTACAAATAATCAAAAAATTAACTGGGCATGGTGGCTCACATCTGTGGTCCCG TAGACCTCATCTCTACAAATAATCAAAAAATTCACTGGGCATGGTGGCTCACATCTGTGGTCCCG T G AC087632.2 Ensembl:ENSG00000259316 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs577558553 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4327861,Human_RBP_ID_17863860 38995 RMVar_ID_38995 Human_SNP_ID_580693994 A-to-I Human chr15 - 64361594 64361592 64361594 TGGAGGCTGAGGCGGGAGGATCGCTTGAGCTCAGGAGTTGGAGACCAGCCTGGGCAACATAGACC TGGAGGCTGAGGCGGGAGGATCGCTTGAGCTC__GAGTTGGAGACCAGCCTGGGCAACATAGACC CCT C AC087632.2 Ensembl:ENSG00000259316 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1464209235 Functional Loss DEL dbSNP153 33..34 33 - - - 38996 RMVar_ID_38996 Human_SNP_ID_580694222 A-to-I Human chr15 - 64362471 64362471 64362471 TCAGCTCACTGCAGCCTCAACCTCCCTTGCTCAAGTGATCCTCCTGCCTCAGCCTCCTGAGTAGC TCAGCTCACTGCAGCCTCAACCTCCCTTGCTCGAGTGATCCTCCTGCCTCAGCCTCCTGAGTAGC T C AC087632.2 Ensembl:ENSG00000259316 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs377751599 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12552207 38997 RMVar_ID_38997 Human_SNP_ID_580694228 A-to-I Human chr15 - 64362534 64362534 64362534 GATTGATTGATTTTGAGGCAGGATCTTACTCTATTGCCCAGGCCAGAGTGCAGTGGTGTGATCTC GATTGATTGATTTTGAGGCAGGATCTTACTCTGTTGCCCAGGCCAGAGTGCAGTGGTGTGATCTC T C AC087632.2 Ensembl:ENSG00000259316 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170660622 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20042140 38998 RMVar_ID_38998 Human_SNP_ID_580694349 A-to-I Human chr15 - 64362926 64362926 64362926 TAAAATAAATAAATAATAAAAATGCAAAAATTAGCTGGGCAGGGTGGTACATGCCTGTAGTCCCA TAAAATAAATAAATAATAAAAATGCAAAAATTCGCTGGGCAGGGTGGTACATGCCTGTAGTCCCA T G AC087632.2 Ensembl:ENSG00000259316 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs773734929 Functional Loss SNV dbSNP153 33..33 33 - - - 38999 RMVar_ID_38999 Human_SNP_ID_580694911 A-to-I Human chr15 - 64365091 64365091 64365091 GGCTGAGGCAGGAGAATGGCGTGAACCCGGGAAGTGGAGCTTGCAGTGAGCCGAGATTGCGCCAC GGCTGAGGCAGGAGAATGGCGTGAACCCGGGAGGTGGAGCTTGCAGTGAGCCGAGATTGCGCCAC T C AC087632.2,PCLAF Ensembl:ENSG00000259316,Ensembl:ENSG00000166803 Protein coding,Protein coding intron,3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1279037943 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4327869 39000 RMVar_ID_39000 Human_SNP_ID_580694927 A-to-I Human chr15 - 64365141 64365141 64365141 AAAATTAGCCGGGCGCGGTGGCGGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTAGCCGGGCGCGGTGGCGGGCGCCTGTGGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA T C AC087632.2,PCLAF Ensembl:ENSG00000259316,Ensembl:ENSG00000166803 Protein coding,Protein coding intron,3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1196255028 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_275506,Human_miRNA_ID_1356721 39001 RMVar_ID_39001 Human_SNP_ID_580694969 A-to-I Human chr15 - 64365274 64365274 64365274 TTTTTAGCCGGGTGCGGTGGCTCACGCCTGTAATCCCAGCACTCTGGGAGGCCGAGGCGGGTGGA TTTTTAGCCGGGTGCGGTGGCTCACGCCTGTAGTCCCAGCACTCTGGGAGGCCGAGGCGGGTGGA T C AC087632.2,PCLAF Ensembl:ENSG00000259316,Ensembl:ENSG00000166803 Protein coding,Protein coding intron,3'UTR GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829 esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line - 29796672,31158229 RNA-Seq:(High) rs1028279137 Functional Loss SNV dbSNP153 33..33 33 - - - 39002 RMVar_ID_39002 Human_SNP_ID_580694970 A-to-I Human chr15 - 64365283 64365277 64365284 CTAAAACAATTTTTAGCCGGGTGCGGTGGCTCACGCCTGTAATCCCAGCACTCTGGGAGGCCGAG CTAAAACAATTTTTAGCCGGGTGCGGTGGCT_______GTAATCCCAGCACTCTGGGAGGCCGAG CAGGCGTG C AC087632.2,PCLAF Ensembl:ENSG00000259316,Ensembl:ENSG00000166803 Protein coding,Protein coding intron,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1292143049 Functional Loss DEL dbSNP153 32..38 33 - - - Human_RBP_ID_17863873 39003 RMVar_ID_39003 Human_SNP_ID_580695370 A-to-I Human chr15 - 64366934 64366934 64366934 GACAGGCTCTCTGTCCCCGAGGCTGGAGTGCAATGGCACAGTCTCAGCTCACTTCAAGCTCCACC GACAGGCTCTCTGTCCCCGAGGCTGGAGTGCAGTGGCACAGTCTCAGCTCACTTCAAGCTCCACC T C AC087632.2,PCLAF Ensembl:ENSG00000259316,Ensembl:ENSG00000166803 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1282749652 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_759475,Human_RBP_ID_12552276 RMVar_hsa_circ_38666 39004 RMVar_ID_39004 Human_SNP_ID_580695710 A-to-I Human chr15 - 64368170 64368170 64368170 CAGCTAATTGTTTTTGTATTTTTAGTAGAGACAGGGTTTCATTATGTTGGCTAGACTGGTCTCGA CAGCTAATTGTTTTTGTATTTTTAGTAGAGACCGGGTTTCATTATGTTGGCTAGACTGGTCTCGA T G AC087632.2,PCLAF Ensembl:ENSG00000259316,Ensembl:ENSG00000166803 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1231279850 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38666 39005 RMVar_ID_39005 Human_SNP_ID_580695712 A-to-I Human chr15 - 64368176 64368176 64368176 CATGCCCAGCTAATTGTTTTTGTATTTTTAGTAGAGACAGGGTTTCATTATGTTGGCTAGACTGG CATGCCCAGCTAATTGTTTTTGTATTTTTAGTGGAGACAGGGTTTCATTATGTTGGCTAGACTGG T C AC087632.2,PCLAF Ensembl:ENSG00000259316,Ensembl:ENSG00000166803 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1343511083 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38666 39006 RMVar_ID_39006 Human_SNP_ID_580696064 A-to-I Human chr15 - 64369662 64369662 64369662 CATGTGATCTCAGCTACTGGGGAGGCTGAGATAGGAGAATCACTTGAACCTGGGAGGCAGAGGTT CATGTGATCTCAGCTACTGGGGAGGCTGAGATGGGAGAATCACTTGAACCTGGGAGGCAGAGGTT T C AC087632.2,PCLAF Ensembl:ENSG00000259316,Ensembl:ENSG00000166803 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1293466918 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38666 39007 RMVar_ID_39007 Human_SNP_ID_580696340 A-to-I Human chr15 - 64370635 64370635 64370635 CCTGGGTGCGGTGGCTTGTGCCTGTAATCCCAACATTTTGAAAGTCCAAGGCAGGTGGATCACCC CCTGGGTGCGGTGGCTTGTGCCTGTAATCCCAGCATTTTGAAAGTCCAAGGCAGGTGGATCACCC T C AC087632.2,PCLAF Ensembl:ENSG00000259316,Ensembl:ENSG00000166803 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1207810312 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12552382 RMVar_hsa_circ_38666 39008 RMVar_ID_39008 Human_SNP_ID_580696620 A-to-I Human chr15 - 64371469 64371469 64371469 CTGAGGTCAGGAGTTTGAGACTAACCTGGCCAAAATGGTGAAACCCCATCTGTACTAAAAATACA CTGAGGTCAGGAGTTTGAGACTAACCTGGCCAGAATGGTGAAACCCCATCTGTACTAAAAATACA T C AC087632.2,PCLAF Ensembl:ENSG00000259316,Ensembl:ENSG00000166803 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1024100319 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38666 39009 RMVar_ID_39009 Human_SNP_ID_580696721 A-to-I Human chr15 - 64371879 64371879 64371879 AAAAAAGTTGATCTGGGCCAGGTGCGGTGGCTAATGCCTGTAATCCCAGCACTTTGGGAGGCCAA AAAAAAGTTGATCTGGGCCAGGTGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAA T G AC087632.2,PCLAF Ensembl:ENSG00000259316,Ensembl:ENSG00000166803 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1233856287 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38666 39010 RMVar_ID_39010 Human_SNP_ID_580697553 A-to-I Human chr15 - 64375262 64375262 64375262 AAATTAGCCGGGCGTGGTGGCACGTGCCTGTAATCTCAGCTACTCGGGAGGCTGAAGCAGGAGAA AAATTAGCCGGGCGTGGTGGCACGTGCCTGTAGTCTCAGCTACTCGGGAGGCTGAAGCAGGAGAA T C AC087632.2,PCLAF Ensembl:ENSG00000259316,Ensembl:ENSG00000166803 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs890929069 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63713,RMVar_hsa_circ_38666 39011 RMVar_ID_39011 Human_SNP_ID_580697554 A-to-I Human chr15 - 64375263 64375263 64375263 AAAATTAGCCGGGCGTGGTGGCACGTGCCTGTAATCTCAGCTACTCGGGAGGCTGAAGCAGGAGA AAAATTAGCCGGGCGTGGTGGCACGTGCCTGTGATCTCAGCTACTCGGGAGGCTGAAGCAGGAGA T C AC087632.2,PCLAF Ensembl:ENSG00000259316,Ensembl:ENSG00000166803 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1015783502 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63713,RMVar_hsa_circ_38666 39012 RMVar_ID_39012 Human_SNP_ID_580697584 A-to-I Human chr15 - 64375380 64375380 64375380 CAGTGGCTCACCTCTGTAATCCCAGCACTTTGAGAGTCCAAGGCAGGCAGATCACAAGATCAAGA CAGTGGCTCACCTCTGTAATCCCAGCACTTTGCGAGTCCAAGGCAGGCAGATCACAAGATCAAGA T G AC087632.2,PCLAF Ensembl:ENSG00000259316,Ensembl:ENSG00000166803 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs968950308 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63713,RMVar_hsa_circ_38666 39013 RMVar_ID_39013 Human_SNP_ID_580697585 A-to-I Human chr15 - 64375386 64375386 64375386 CTGGCACAGTGGCTCACCTCTGTAATCCCAGCACTTTGAGAGTCCAAGGCAGGCAGATCACAAGA CTGGCACAGTGGCTCACCTCTGTAATCCCAGCTCTTTGAGAGTCCAAGGCAGGCAGATCACAAGA T A AC087632.2,PCLAF Ensembl:ENSG00000259316,Ensembl:ENSG00000166803 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1264813701 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12552482,Human_RBP_ID_17563079 RMVar_hsa_circ_63713,RMVar_hsa_circ_38666 39014 RMVar_ID_39014 Human_SNP_ID_580697615 A-to-I Human chr15 - 64375539 64375539 64375539 AAAGGGTGGCGGCGCCGCCTATAATCCCAGCCACTAGGGAGGCTGAGGTGGGAGAATTGCTTGAC AAAGGGTGGCGGCGCCGCCTATAATCCCAGCCGCTAGGGAGGCTGAGGTGGGAGAATTGCTTGAC T C AC087632.2,PCLAF Ensembl:ENSG00000259316,Ensembl:ENSG00000166803 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1344558476 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63713,RMVar_hsa_circ_38666 39015 RMVar_ID_39015 Human_SNP_ID_580697710 A-to-I Human chr15 - 64376077 64376077 64376077 GGGATTACAGGCACACGCCACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTTG GGGATTACAGGCACACGCCACCACGCCCAGCTGATTTTTGTATTTTTAGTAGAGACAGGGTTTTG T C AC087632.2,PCLAF Ensembl:ENSG00000259316,Ensembl:ENSG00000166803 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs920245368 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63713,RMVar_hsa_circ_38666 39016 RMVar_ID_39016 Human_SNP_ID_580697737 A-to-I Human chr15 - 64376194 64376194 64376194 CTGAGACGGAGTCTTGCTCTGTTGCCCAGGCTAGAGGGCAGTGGCGCTATCTCAGCTCACTGCAA CTGAGACGGAGTCTTGCTCTGTTGCCCAGGCTGGAGGGCAGTGGCGCTATCTCAGCTCACTGCAA T C AC087632.2,PCLAF Ensembl:ENSG00000259316,Ensembl:ENSG00000166803 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs973979007 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12656213 RMVar_hsa_circ_63713,RMVar_hsa_circ_38666 39017 RMVar_ID_39017 Human_SNP_ID_580697847 A-to-I Human chr15 - 64376622 64376622 64376622 TTGAGGCCAGGAGTTCAAAACCAGCCTGTCCAACATGGTGGAACCCTGTCTCTACTAAAAATACA TTGAGGCCAGGAGTTCAAAACCAGCCTGTCCAGCATGGTGGAACCCTGTCTCTACTAAAAATACA T C AC087632.2,PCLAF Ensembl:ENSG00000259316,Ensembl:ENSG00000166803 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs965786170 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63713,RMVar_hsa_circ_38666 39018 RMVar_ID_39018 Human_SNP_ID_580697992 A-to-I Human chr15 - 64377233 64377233 64377233 TCGAACTCCTGACCTTGTGATCCACCCTCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG TCGAACTCCTGACCTTGTGATCCACCCTCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG T C AC087632.2,PCLAF Ensembl:ENSG00000259316,Ensembl:ENSG00000166803 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs568934161 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15663 39019 RMVar_ID_39019 Human_SNP_ID_580698321 A-to-I Human chr15 - 64377889 64377889 64377889 AAATTAGCTGGGCGTGGTGGCGGGCGCCTGTAATCCCTGCTACTCGGGAGGCTGAGGCAGGAGAA AAATTAGCTGGGCGTGGTGGCGGGCGCCTGTAGTCCCTGCTACTCGGGAGGCTGAGGCAGGAGAA T C AC087632.2,PCLAF Ensembl:ENSG00000259316,Ensembl:ENSG00000166803 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1360603549 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15663 39020 RMVar_ID_39020 Human_SNP_ID_580698431 A-to-I Human chr15 - 64378205 64378205 64378205 TAACCAGGAATTGGCCGGGCAGGGTGGCTCACACTTGTAATCCCAGCACTTTGGGAGGCCAAGGC TAACCAGGAATTGGCCGGGCAGGGTGGCTCACGCTTGTAATCCCAGCACTTTGGGAGGCCAAGGC T C AC087632.2,PCLAF Ensembl:ENSG00000259316,Ensembl:ENSG00000166803 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1566967005 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15663 39021 RMVar_ID_39021 Human_SNP_ID_580701633 A-to-I Human chr15 + 64389899 64389899 64389899 AATTTTTGTATTCTTACTAGAGATGGGGTTTCACCATGTTGACCAGGGTGGTCTCGAACTCCTGA AATTTTTGTATTCTTACTAGAGATGGGGTTTCGCCATGTTGACCAGGGTGGTCTCGAACTCCTGA A G TRIP4 Ensembl:ENSG00000103671 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1299640579 Functional Loss SNV dbSNP153 33..33 33 - - - 39022 RMVar_ID_39022 Human_SNP_ID_580702105 A-to-I Human chr15 + 64391318 64391318 64391318 AGCTTGGACTACAGGCGCGTGACACCATGCCCAGCTAATTTTTGTATTTTTAGTGGAGATGGGAT AGCTTGGACTACAGGCGCGTGACACCATGCCCGGCTAATTTTTGTATTTTTAGTGGAGATGGGAT A G TRIP4 Ensembl:ENSG00000103671 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1473110916 Functional Loss SNV dbSNP153 33..33 33 - - - 39023 RMVar_ID_39023 Human_SNP_ID_580702328 A-to-I Human chr15 + 64392035 64392035 64392035 CAGCGGCTCAGCCTGTAATTCCAGCACTTTGGAAGGCTGAGGCGGGCAAATCACTTGAGGTCAGG CAGCGGCTCAGCCTGTAATTCCAGCACTTTGGCAGGCTGAGGCGGGCAAATCACTTGAGGTCAGG A C TRIP4 Ensembl:ENSG00000103671 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs532714040 Functional Loss SNV dbSNP153 33..33 33 - - - 39024 RMVar_ID_39024 Human_SNP_ID_580702513 A-to-I Human chr15 + 64392680 64392680 64392680 ATTCTGTTGCTCAGGCTGGAATGTAGTGGTGCAATCATGGCTCTGCAGCCTTCACCTCTGAGACT ATTCTGTTGCTCAGGCTGGAATGTAGTGGTGCGATCATGGCTCTGCAGCCTTCACCTCTGAGACT A G TRIP4 Ensembl:ENSG00000103671 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1007859112 Functional Loss SNV dbSNP153 33..33 33 - - - 39025 RMVar_ID_39025 Human_SNP_ID_580704588 A-to-I Human chr15 + 64400185 64400185 64400185 GAACCAGAAGCCAGGTATGGTGGCTGATGCCTATAATCCCATTGCTTTCGGAGGCTGAGGAGGGA GAACCAGAAGCCAGGTATGGTGGCTGATGCCTGTAATCCCATTGCTTTCGGAGGCTGAGGAGGGA A G TRIP4 Ensembl:ENSG00000103671 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006655194 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35001,RMVar_hsa_circ_64915,RMVar_hsa_circ_318822,RMVar_hsa_circ_354200,RMVar_hsa_circ_363524,RMVar_hsa_circ_331552,RMVar_hsa_circ_329476,RMVar_hsa_circ_291720,RMVar_hsa_circ_318008,RMVar_hsa_circ_173040,RMVar_hsa_circ_173042,RMVar_hsa_circ_173043,RMVar_hsa_circ_173041,RMVar_hsa_circ_328125,RMVar_hsa_circ_292470 39026 RMVar_ID_39026 Human_SNP_ID_580710167 A-to-I Human chr15 + 64421922 64421922 64421922 CAAAAATTAGCGGAGCATGGTGGTGCATGCCTATAATTCTAGCTACTCGGGAGGCTGAGGCAGGA CAAAAATTAGCGGAGCATGGTGGTGCATGCCTGTAATTCTAGCTACTCGGGAGGCTGAGGCAGGA A G TRIP4 Ensembl:ENSG00000103671 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1019647365 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_318822,RMVar_hsa_circ_329476,RMVar_hsa_circ_318008,RMVar_hsa_circ_173042,RMVar_hsa_circ_173043,RMVar_hsa_circ_173049,RMVar_hsa_circ_173044,RMVar_hsa_circ_86493,RMVar_hsa_circ_334517,RMVar_hsa_circ_63466,RMVar_hsa_circ_365447,RMVar_hsa_circ_335233,RMVar_hsa_circ_350825,RMVar_hsa_circ_279542,RMVar_hsa_circ_68110,RMVar_hsa_circ_272124,RMVar_hsa_circ_332640,RMVar_hsa_circ_173050 39027 RMVar_ID_39027 Human_SNP_ID_580710168 A-to-I Human chr15 + 64421922 64421922 64421922 CAAAAATTAGCGGAGCATGGTGGTGCATGCCTATAATTCTAGCTACTCGGGAGGCTGAGGCAGGA CAAAAATTAGCGGAGCATGGTGGTGCATGCCTTTAATTCTAGCTACTCGGGAGGCTGAGGCAGGA A T TRIP4 Ensembl:ENSG00000103671 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1019647365 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_318822,RMVar_hsa_circ_329476,RMVar_hsa_circ_318008,RMVar_hsa_circ_173042,RMVar_hsa_circ_173043,RMVar_hsa_circ_173049,RMVar_hsa_circ_173044,RMVar_hsa_circ_86493,RMVar_hsa_circ_334517,RMVar_hsa_circ_63466,RMVar_hsa_circ_365447,RMVar_hsa_circ_335233,RMVar_hsa_circ_350825,RMVar_hsa_circ_279542,RMVar_hsa_circ_68110,RMVar_hsa_circ_272124,RMVar_hsa_circ_332640,RMVar_hsa_circ_173050 39028 RMVar_ID_39028 Human_SNP_ID_580711538 A-to-I Human chr15 + 64427488 64427488 64427488 ACCTCTGCCTCCTGGGCTTAAGTGATCCTCCCACCTCAGCCTCCCAGTAGCTGGGACTACAGGCA ACCTCTGCCTCCTGGGCTTAAGTGATCCTCCCCCCTCAGCCTCCCAGTAGCTGGGACTACAGGCA A C TRIP4 Ensembl:ENSG00000103671 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs536618086 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_318008,RMVar_hsa_circ_173043,RMVar_hsa_circ_63466,RMVar_hsa_circ_335233,RMVar_hsa_circ_350825,RMVar_hsa_circ_332640,RMVar_hsa_circ_334759 39029 RMVar_ID_39029 Human_SNP_ID_580711539 A-to-I Human chr15 + 64427488 64427488 64427488 ACCTCTGCCTCCTGGGCTTAAGTGATCCTCCCACCTCAGCCTCCCAGTAGCTGGGACTACAGGCA ACCTCTGCCTCCTGGGCTTAAGTGATCCTCCCTCCTCAGCCTCCCAGTAGCTGGGACTACAGGCA A T TRIP4 Ensembl:ENSG00000103671 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs536618086 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_318008,RMVar_hsa_circ_173043,RMVar_hsa_circ_63466,RMVar_hsa_circ_335233,RMVar_hsa_circ_350825,RMVar_hsa_circ_332640,RMVar_hsa_circ_334759 39030 RMVar_ID_39030 Human_SNP_ID_580713909 A-to-I Human chr15 + 64436430 64436430 64436430 CCTGGGCAGCATGGTGAAACCCTGTCTCTACTAAGAATATAAAAATTAGTTGGGCATGGTGGCGG CCTGGGCAGCATGGTGAAACCCTGTCTCTACTGAGAATATAAAAATTAGTTGGGCATGGTGGCGG A G TRIP4 Ensembl:ENSG00000103671 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1468450548 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_318008,RMVar_hsa_circ_173043,RMVar_hsa_circ_63466,RMVar_hsa_circ_335233,RMVar_hsa_circ_350825,RMVar_hsa_circ_332640,RMVar_hsa_circ_334759 39031 RMVar_ID_39031 Human_SNP_ID_580715384 A-to-I Human chr15 + 64442392 64442391 64442393 ATATTGGATATACTTTGGCTTTTCTTTGAGACAGGGTCTCACTCTGTTGCCCACGCTAGAGTGTG ATATTGGATATACTTTGGCTTTTCTTTGAGAC__GGTCTCACTCTGTTGCCCACGCTAGAGTGTG CAG C TRIP4 Ensembl:ENSG00000103671 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1443209655 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_318008,RMVar_hsa_circ_173043,RMVar_hsa_circ_63466,RMVar_hsa_circ_335233,RMVar_hsa_circ_350825,RMVar_hsa_circ_332640,RMVar_hsa_circ_334759 39032 RMVar_ID_39032 Human_SNP_ID_580716993 A-to-I Human chr15 + 64449089 64449089 64449089 AAAAAATTATTCCAGTGTGGTGGCGTGTGCCTATAGTGCCAGCTACTTGGGAGGCTGAGGCAGAA AAAAAATTATTCCAGTGTGGTGGCGTGTGCCTGTAGTGCCAGCTACTTGGGAGGCTGAGGCAGAA A G TRIP4 Ensembl:ENSG00000103671 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1466295724 Functional Loss SNV dbSNP153 33..33 33 - - - 39033 RMVar_ID_39033 Human_SNP_ID_580716996 A-to-I Human chr15 + 64449091 64449091 64449091 AAAATTATTCCAGTGTGGTGGCGTGTGCCTATAGTGCCAGCTACTTGGGAGGCTGAGGCAGAAAT AAAATTATTCCAGTGTGGTGGCGTGTGCCTATGGTGCCAGCTACTTGGGAGGCTGAGGCAGAAAT A G TRIP4 Ensembl:ENSG00000103671 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1391520524 Functional Loss SNV dbSNP153 33..33 33 - - - 39034 RMVar_ID_39034 Human_SNP_ID_580720822 A-to-I Human chr15 + 64465628 64465628 64465628 CTGTAGAGCTCCTGACCTCAGGTGATCCACCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGT CTGTAGAGCTCCTGACCTCAGGTGATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGT A G ZNF609 Ensembl:ENSG00000180357 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1315126683 Functional Loss SNV dbSNP153 33..33 33 - - - 39035 RMVar_ID_39035 Human_SNP_ID_580721385 A-to-I Human chr15 + 64467734 64467734 64467734 GGGCATGGTGGCGCACGTCTGTAGTCCCAGCTACTCGGGAGGCTGAGGAAGGATGATTGCTTGAA GGGCATGGTGGCGCACGTCTGTAGTCCCAGCTGCTCGGGAGGCTGAGGAAGGATGATTGCTTGAA A G ZNF609 Ensembl:ENSG00000180357 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1467216501 Functional Loss SNV dbSNP153 33..33 33 - - - 39036 RMVar_ID_39036 Human_SNP_ID_580721812 A-to-I Human chr15 + 64469182 64469182 64469182 CTACTTGGGAGGCTGAGGCAGGAGAATCGCTTAAACTTGGGAGGTAGAAGTTGCAGTGAGCCGAG CTACTTGGGAGGCTGAGGCAGGAGAATCGCTTCAACTTGGGAGGTAGAAGTTGCAGTGAGCCGAG A C ZNF609 Ensembl:ENSG00000180357 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879195766 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12553000 39037 RMVar_ID_39037 Human_SNP_ID_580721813 A-to-I Human chr15 + 64469182 64469182 64469182 CTACTTGGGAGGCTGAGGCAGGAGAATCGCTTAAACTTGGGAGGTAGAAGTTGCAGTGAGCCGAG CTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAACTTGGGAGGTAGAAGTTGCAGTGAGCCGAG A G ZNF609 Ensembl:ENSG00000180357 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879195766 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12553000 39038 RMVar_ID_39038 Human_SNP_ID_580725196 A-to-I Human chr15 + 64481460 64481460 64481460 CTTCTGCCTCAGCCTCCCTAGTAGCTAGGATTACAGGCATGTGACACCACGCCTAGCTAATTCTG CTTCTGCCTCAGCCTCCCTAGTAGCTAGGATTGCAGGCATGTGACACCACGCCTAGCTAATTCTG A G ZNF609 Ensembl:ENSG00000180357 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs958546107 Functional Loss SNV dbSNP153 33..33 33 - - - 39039 RMVar_ID_39039 Human_SNP_ID_580726629 A-to-I Human chr15 + 64486709 64486709 64486709 ATGATCTCAGGTCAATGTAGCCTCTGCTTCCCAGGTTCAAGTGATTCTCATGCCTCAGCCTCCTG ATGATCTCAGGTCAATGTAGCCTCTGCTTCCCGGGTTCAAGTGATTCTCATGCCTCAGCCTCCTG A G ZNF609 Ensembl:ENSG00000180357 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1566995791 Functional Loss SNV dbSNP153 33..33 33 - - - 39040 RMVar_ID_39040 Human_SNP_ID_580729427 A-to-I Human chr15 + 64497786 64497786 64497786 AGTCAGTCATTGTGGTGCACGCCTGTAATCCCAACCTCTTGGGAGGCTGAGGTGGGAGAATTGCT AGTCAGTCATTGTGGTGCACGCCTGTAATCCCCACCTCTTGGGAGGCTGAGGTGGGAGAATTGCT A C ZNF609 Ensembl:ENSG00000180357 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1461067581 Functional Loss SNV dbSNP153 33..33 33 - - - 39041 RMVar_ID_39041 Human_SNP_ID_580733268 A-to-I Human chr15 + 64514663 64514663 64514663 CTAAACTATGCTTTTTTTTTTTTTTGAGACGGAGTCTCACTCTGTCATCCCAGGCTAGAGTGCAG CTAAACTATGCTTTTTTTTTTTTTTGAGACGGTGTCTCACTCTGTCATCCCAGGCTAGAGTGCAG A T ZNF609 Ensembl:ENSG00000180357 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1280810195 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120107,RMVar_hsa_circ_173052 39042 RMVar_ID_39042 Human_SNP_ID_580733297 A-to-I Human chr15 + 64514804 64514804 64514804 GGAATTACAAGTGTGCACCACCACACCTGGCTAGTTGTTGTATTTTTTGTAGAGATGGGTTTCAC GGAATTACAAGTGTGCACCACCACACCTGGCTCGTTGTTGTATTTTTTGTAGAGATGGGTTTCAC A C ZNF609 Ensembl:ENSG00000180357 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1281281765 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120107,RMVar_hsa_circ_173052 39043 RMVar_ID_39043 Human_SNP_ID_580738270 A-to-I Human chr15 + 64536660 64536660 64536660 GCACTTTGGGAGGCCGAGGCAGGAGGATCACTAGAGCTAAGGAGTTCGAGATCAGCCTGGGCAAC GCACTTTGGGAGGCCGAGGCAGGAGGATCACTGGAGCTAAGGAGTTCGAGATCAGCCTGGGCAAC A G ZNF609 Ensembl:ENSG00000180357 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs929036068 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120107,RMVar_hsa_circ_173052 39044 RMVar_ID_39044 Human_SNP_ID_580739202 A-to-I Human chr15 + 64539468 64539468 64539468 TGACCGCGTGATCCACCCGCCTTGGCCTCCCCAAGTGCTGGGATTACAGGCGTGAGCCACTGCGC TGACCGCGTGATCCACCCGCCTTGGCCTCCCCCAGTGCTGGGATTACAGGCGTGAGCCACTGCGC A C ZNF609 Ensembl:ENSG00000180357 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1422571571 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120107,RMVar_hsa_circ_173052 39045 RMVar_ID_39045 Human_SNP_ID_580740063 A-to-I Human chr15 + 64542014 64542014 64542014 CCCTTTAAAAAATAGGTTGAGTTGGGCATGGTAGTATAGACCTGTAATTCCAGCTATTCAGGGAG CCCTTTAAAAAATAGGTTGAGTTGGGCATGGTCGTATAGACCTGTAATTCCAGCTATTCAGGGAG A C ZNF609 Ensembl:ENSG00000180357 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs750083373 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12554121,Human_RBP_ID_22496508 RMVar_hsa_circ_120107,RMVar_hsa_circ_173052 39046 RMVar_ID_39046 Human_SNP_ID_580740064 A-to-I Human chr15 + 64542014 64542014 64542014 CCCTTTAAAAAATAGGTTGAGTTGGGCATGGTAGTATAGACCTGTAATTCCAGCTATTCAGGGAG CCCTTTAAAAAATAGGTTGAGTTGGGCATGGTGGTATAGACCTGTAATTCCAGCTATTCAGGGAG A G ZNF609 Ensembl:ENSG00000180357 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs750083373 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12554121,Human_RBP_ID_22496508 RMVar_hsa_circ_120107,RMVar_hsa_circ_173052 39047 RMVar_ID_39047 Human_SNP_ID_580741699 A-to-I Human chr15 + 64548645 64548645 64548645 CAAAAATTACTTGGGCATAGTAGTATGTGCCTATATTCCCAGCTACTTGGGAGGCTAAAGTAGGA CAAAAATTACTTGGGCATAGTAGTATGTGCCTGTATTCCCAGCTACTTGGGAGGCTAAAGTAGGA A G ZNF609 Ensembl:ENSG00000180357 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1284385251 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120107,RMVar_hsa_circ_173052 39048 RMVar_ID_39048 Human_SNP_ID_580751502 A-to-I Human chr15 + 64584561 64584561 64584561 GACCTCAAGTAATCCACCCACCCAGCCTCTCAAAGTGCTGGGATTACAGGAATGAGCCACCACAC GACCTCAAGTAATCCACCCACCCAGCCTCTCACAGTGCTGGGATTACAGGAATGAGCCACCACAC A C ZNF609 Ensembl:ENSG00000180357 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1281874738 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120107,RMVar_hsa_circ_173052 39049 RMVar_ID_39049 Human_SNP_ID_580752981 A-to-I Human chr15 + 64590502 64590502 64590502 TGCCACCACACCCAGCTAATTTTTGTGTTAGTAGAGTTGGGGTTTTGCCATGTTAGCCAGGCTGG TGCCACCACACCCAGCTAATTTTTGTGTTAGTGGAGTTGGGGTTTTGCCATGTTAGCCAGGCTGG A G ZNF609 Ensembl:ENSG00000180357 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs933650148 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120107,RMVar_hsa_circ_173052 39050 RMVar_ID_39050 Human_SNP_ID_580753373 A-to-I Human chr15 + 64592029 64592029 64592029 CCACACCCGGCCTTTTTTTAATCAGCTGGTGGAATGTGCCTGTGGTCTCAGCTACTTGGCAGACT CCACACCCGGCCTTTTTTTAATCAGCTGGTGGGATGTGCCTGTGGTCTCAGCTACTTGGCAGACT A G ZNF609 Ensembl:ENSG00000180357 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs929325673 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120107,RMVar_hsa_circ_173052 39051 RMVar_ID_39051 Human_SNP_ID_580753628 A-to-I Human chr15 + 64593030 64593030 64593030 ACAATGGTCGTGCCAAAAAGGGCCGCGGCCACATGCAGCCTATTCGCTGCACTAACTGTGCCCGA ACAATGGTCGTGCCAAAAAGGGCCGCGGCCACGTGCAGCCTATTCGCTGCACTAACTGTGCCCGA A G ZNF609,AC090543.3 Ensembl:ENSG00000180357,Ensembl:ENSG00000243403 Protein coding,Pseudogene intron,exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs933725984 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_123621,Human_RBP_ID_460925,Human_RBP_ID_8251490 RMVar_hsa_circ_120107,RMVar_hsa_circ_173052 39052 RMVar_ID_39052 Human_SNP_ID_580763307 A-to-I Human chr15 + 64628504 64628504 64628504 TATGGTGAAACCCCGTCTCTACTACAAAAATTAGCCAGGTGTGGTGATACATGCCTGTAATCCCA TATGGTGAAACCCCGTCTCTACTACAAAAATTTGCCAGGTGTGGTGATACATGCCTGTAATCCCA A T ZNF609 Ensembl:ENSG00000180357 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs529894694 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35697,RMVar_hsa_circ_370522,RMVar_hsa_circ_173054 39053 RMVar_ID_39053 Human_SNP_ID_580775203 A-to-I Human chr15 + 64675219 64675219 64675219 CAGACCCCCACCAAAGCCGACTGGCTAGCATCAAGGCTGAAGCCGACAAGATCTACAGTTTCACG CAGACCCCCACCAAAGCCGACTGGCTAGCATCGAGGCTGAAGCCGACAAGATCTACAGTTTCACG A G ZNF609 Ensembl:ENSG00000180357 Protein coding CDS GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs148923023 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26326856,Human_RBP_ID_26809475 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 39054 RMVar_ID_39054 Human_SNP_ID_580780291 A-to-I Human chr15 + 64694034 64694034 64694034 TGGAGGCTGCAGTTAGCCGAGATTGTGCCACTACACTCTAGCCTGGGTGACAGAGCCAGATTCCT TGGAGGCTGCAGTTAGCCGAGATTGTGCCACTGCACTCTAGCCTGGGTGACAGAGCCAGATTCCT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334584198 Functional Loss SNV dbSNP153 33..33 33 - - - 39055 RMVar_ID_39055 Human_SNP_ID_580808494 A-to-I Human chr15 + 64790428 64790428 64790428 CAAGGAGTTCGAGGTTGCAGTGACCTTTGATCATGCCATTGCACTCCAGCCTGGGCAACAGAGAA CAAGGAGTTCGAGGTTGCAGTGACCTTTGATCGTGCCATTGCACTCCAGCCTGGGCAACAGAGAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1007774507 Functional Loss SNV dbSNP153 33..33 33 - - - 39056 RMVar_ID_39056 Human_SNP_ID_580819926 A-to-I Human chr15 + 64828936 64828936 64828936 CATAACTCACTGCCGCCTTGACCTTCCTGCTCAAGTGATCCTCCCATCTCAGCCTCCCAAGTAGT CATAACTCACTGCCGCCTTGACCTTCCTGCTCCAGTGATCCTCCCATCTCAGCCTCCCAAGTAGT A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs757410838 Functional Loss SNV dbSNP153 33..33 33 - - - 39057 RMVar_ID_39057 Human_SNP_ID_580846360 A-to-I Human chr15 + 64931968 64931968 64931968 CAGGCTGAAGTGCAATGGTGCGATCTTGGCTCACTGTAACCTCCGCCTCCTGGGTTCAAGCAGTT CAGGCTGAAGTGCAATGGTGCGATCTTGGCTCGCTGTAACCTCCGCCTCCTGGGTTCAAGCAGTT A G ANKDD1A Ensembl:ENSG00000166839 Protein coding exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1346396346 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18082,RMVar_hsa_circ_285017,RMVar_hsa_circ_275596 39058 RMVar_ID_39058 Human_SNP_ID_580856843 A-to-I Human chr15 - 64956729 64956729 64956729 CACCAACATGGTGAAACCTGTCTACTAAAAATACAAAAATTAGCCGGGCATGATGGTGTGTGCTT CACCAACATGGTGAAACCTGTCTACTAAAAATGCAAAAATTAGCCGGGCATGATGGTGTGTGCTT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs529195449 Functional Loss SNV dbSNP153 33..33 33 - - - 39059 RMVar_ID_39059 Human_SNP_ID_580857007 A-to-I Human chr15 - 64957222 64957222 64957222 CAAACCCCATCTCTACTAAAAATACAAAAATTAGCCAGCTGTGATGGCATGCACCTGTAATCCCA CAAACCCCATCTCTACTAAAAATACAAAAATTGGCCAGCTGTGATGGCATGCACCTGTAATCCCA T C - - Other Unknown GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1174939521 Functional Loss SNV dbSNP153 33..33 33 - - - 39060 RMVar_ID_39060 Human_SNP_ID_580857601 A-to-I Human chr15 - 64959541 64959541 64959541 AAAATTAGCTGGGCGTGGTGGCATGTGCCTGTAATTCCATCTACTTGGGAGGCTGAAGAGGAGAA AAAATTAGCTGGGCGTGGTGGCATGTGCCTGTTATTCCATCTACTTGGGAGGCTGAAGAGGAGAA T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1156421052 Functional Loss SNV dbSNP153 33..33 33 - - - 39061 RMVar_ID_39061 Human_SNP_ID_580858319 A-to-I Human chr15 - 64962625 64962625 64962625 GGAGTGCAATGACGTGATCTCGGCTCACCGCAACCTCCGCCTCCCGGGTTCAAGCAATTCTTCTG GGAGTGCAATGACGTGATCTCGGCTCACCGCACCCTCCGCCTCCCGGGTTCAAGCAATTCTTCTG T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs531480372 Functional Loss SNV dbSNP153 33..33 33 - - - 39062 RMVar_ID_39062 Human_SNP_ID_580860559 A-to-I Human chr15 - 64971350 64971350 64971350 TATTTTTAGTGGAGACGGGGTTTCACCGTGTTAGCCAGGATGGTCTCAATCTCCTGACCTCGTGA TATTTTTAGTGGAGACGGGGTTTCACCGTGTTCGCCAGGATGGTCTCAATCTCCTGACCTCGTGA T G SPG21 Ensembl:ENSG00000090487 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1237939160 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60181,RMVar_hsa_circ_329676,RMVar_hsa_circ_337636,RMVar_hsa_circ_340055,RMVar_hsa_circ_300153,RMVar_hsa_circ_338386,RMVar_hsa_circ_290674 39063 RMVar_ID_39063 Human_SNP_ID_580861383 A-to-I Human chr15 - 64974683 64974683 64974683 TTTGGCCCAGAAATTTGCTGAATACACTCACAAATCTCCTAGAGTCCATTCCCTAATCCTCTGCA TTTGGCCCAGAAATTTGCTGAATACACTCACAGATCTCCTAGAGTCCATTCCCTAATCCTCTGCA T C SPG21 Ensembl:ENSG00000090487 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs765005335 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17252773,Human_RBP_ID_17365869,Human_RBP_ID_17483126,Human_RBP_ID_17864064 Human_Splice_Rec_1613790,Human_Splice_Rec_1613791,Human_Splice_Rec_1613802,Human_Splice_Rec_1613803,Human_Splice_Rec_1613818,Human_Splice_Rec_1613819,Human_Splice_Rec_1613846,Human_Splice_Rec_1613847,Human_Splice_Rec_1613864,Human_Splice_Rec_1613874,Human_Splice_Rec_1613880 RMVar_hsa_circ_173086,RMVar_hsa_circ_60181,RMVar_hsa_circ_329676,RMVar_hsa_circ_337636,RMVar_hsa_circ_340055,RMVar_hsa_circ_300153,RMVar_hsa_circ_338386,RMVar_hsa_circ_290674,RMVar_hsa_circ_173088,RMVar_hsa_circ_276164,RMVar_hsa_circ_299089,RMVar_hsa_circ_297923,RMVar_hsa_circ_273316,RMVar_hsa_circ_173087 39064 RMVar_ID_39064 Human_SNP_ID_580863579 A-to-I Human chr15 - 64983078 64983078 64983078 AATTTTTGTATTTTTAGTAGAGGCAGAGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGA AATTTTTGTATTTTTAGTAGAGGCAGAGTTTCTCCATGTTGGCCAGGCTGGTCTCGAACTCCTGA T A SPG21 Ensembl:ENSG00000090487 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1403172625 Functional Loss SNV dbSNP153 33..33 33 - - - 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 39065 RMVar_ID_39065 Human_SNP_ID_580863610 A-to-I Human chr15 - 64983142 64983142 64983142 GAGATTCTCCTGCCTCAACCTGCCAAGTAGCTAGGATTACAGGCATGCGCTACCACACTCAGCTA GAGATTCTCCTGCCTCAACCTGCCAAGTAGCTGGGATTACAGGCATGCGCTACCACACTCAGCTA T C SPG21 Ensembl:ENSG00000090487 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs903604052 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1613908 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 39066 RMVar_ID_39066 Human_SNP_ID_580863619 A-to-I Human chr15 - 64983157 64983157 64983157 GCTTCCCAGGTTCAAGAGATTCTCCTGCCTCAACCTGCCAAGTAGCTAGGATTACAGGCATGCGC GCTTCCCAGGTTCAAGAGATTCTCCTGCCTCAGCCTGCCAAGTAGCTAGGATTACAGGCATGCGC T C SPG21 Ensembl:ENSG00000090487 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1030174335 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1613908 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 39067 RMVar_ID_39067 Human_SNP_ID_580863620 A-to-I Human chr15 - 64983158 64983158 64983158 TGCTTCCCAGGTTCAAGAGATTCTCCTGCCTCAACCTGCCAAGTAGCTAGGATTACAGGCATGCG TGCTTCCCAGGTTCAAGAGATTCTCCTGCCTCGACCTGCCAAGTAGCTAGGATTACAGGCATGCG T C SPG21 Ensembl:ENSG00000090487 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1031286235 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1613908 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 39068 RMVar_ID_39068 Human_SNP_ID_580863934 A-to-I Human chr15 - 64984388 64984387 64984388 TGATTGTGCCATTGAACTGCAGCCTGGACAACAGAGCAAGACTGTCTCAAAAATTAAAAAAGTAA TGATTGTGCCATTGAACTGCAGCCTGGACAAC_GAGCAAGACTGTCTCAAAAATTAAAAAAGTAA CT C SPG21 Ensembl:ENSG00000090487 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs575054893 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_1831786 39069 RMVar_ID_39069 Human_SNP_ID_580864355 A-to-I Human chr15 - 64986194 64986192 64986194 GCCAGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACTACCTTGGCTAGGCTGGTCTTGA GCCAGGCTAATTTTTGTATTTTTAGTAGAGAC__GGTTTCACTACCTTGGCTAGGCTGGTCTTGA CCT C SPG21 Ensembl:ENSG00000090487 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1016841140 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_12555385 39070 RMVar_ID_39070 Human_SNP_ID_580864358 A-to-I Human chr15 - 64986194 64986194 64986194 GCCAGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACTACCTTGGCTAGGCTGGTCTTGA GCCAGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACTACCTTGGCTAGGCTGGTCTTGA T C SPG21 Ensembl:ENSG00000090487 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs571300849 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12555385 39071 RMVar_ID_39071 Human_SNP_ID_580870681 A-to-I Human chr15 - 65011105 65011105 65011105 GTTGACCTGGCTGGTCTCGAACTCCTATCCTCAGGTGATCCACCTGCCTCAGCCTCCCTAAGTGC GTTGACCTGGCTGGTCTCGAACTCCTATCCTCGGGTGATCCACCTGCCTCAGCCTCCCTAAGTGC T C MTFMT Ensembl:ENSG00000103707 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1481675958 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_173095,RMVar_hsa_circ_11491,RMVar_hsa_circ_103001,RMVar_hsa_circ_173093,RMVar_hsa_circ_51546,RMVar_hsa_circ_319700,RMVar_hsa_circ_173094,RMVar_hsa_circ_64963,RMVar_hsa_circ_11422 39072 RMVar_ID_39072 Human_SNP_ID_580872388 A-to-I Human chr15 - 65017676 65017676 65017676 CTCCCACCTCAGCCTCCCAAGTAGCTGGGACTACAGGTACATTCCACCATGCCTGGCTAATTTTT CTCCCACCTCAGCCTCCCAAGTAGCTGGGACTGCAGGTACATTCCACCATGCCTGGCTAATTTTT T C MTFMT Ensembl:ENSG00000103707 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs565526923 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_173095,RMVar_hsa_circ_11491,RMVar_hsa_circ_51546,RMVar_hsa_circ_319700,RMVar_hsa_circ_11422,RMVar_hsa_circ_173097,RMVar_hsa_circ_294548,RMVar_hsa_circ_322118,RMVar_hsa_circ_289475,RMVar_hsa_circ_173096 39073 RMVar_ID_39073 Human_SNP_ID_580875054 A-to-I Human chr15 - 65028300 65028300 65028300 GCAATCATCCCATCTCAGCTTCCAGAGTAGCTAGGACTACGGGCGTGCACCACCACGCCTGATTT GCAATCATCCCATCTCAGCTTCCAGAGTAGCTGGGACTACGGGCGTGCACCACCACGCCTGATTT T C MTFMT Ensembl:ENSG00000103707 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1230660045 Functional Loss SNV dbSNP153 33..33 33 - - - 39074 RMVar_ID_39074 Human_SNP_ID_580895163 A-to-I Human chr15 - 65105848 65105848 65105848 AGGTGGAGGTTGCAGTGAACCAAGATTGTGCCACTGCATTTCAGCCTGGCGACAGAGTGAGACTT AGGTGGAGGTTGCAGTGAACCAAGATTGTGCCGCTGCATTTCAGCCTGGCGACAGAGTGAGACTT T C UBAP1L Ensembl:ENSG00000246922 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank;ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs892839604 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25186563 39075 RMVar_ID_39075 Human_SNP_ID_580895398 A-to-I Human chr15 - 65106733 65106733 65106733 GGGAGGCTGAGGTAGGAGAATCACTTGAACCCAGGAGCTGGAGGTTGCAGTGAGGCAAGATCAGG GGGAGGCTGAGGTAGGAGAATCACTTGAACCCGGGAGCTGGAGGTTGCAGTGAGGCAAGATCAGG T C UBAP1L Ensembl:ENSG00000246922 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1442150744 Functional Loss SNV dbSNP153 33..33 33 - - - 39076 RMVar_ID_39076 Human_SNP_ID_580897242 A-to-I Human chr15 - 65114024 65114024 65114024 AAAATTAGCGGGCGTGGTGGCAGGTGCTTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAA AAAATTAGCGGGCGTGGTGGCAGGTGCTTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAA T C UBAP1L Ensembl:ENSG00000246922 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1235346184 Functional Loss SNV dbSNP153 33..33 33 - - - 39077 RMVar_ID_39077 Human_SNP_ID_580898074 A-to-I Human chr15 - 65117660 65117660 65117660 GGCGTAGGTGGTGCACACCTGTAGTCCCAGCTACTGGGGAGGCTGAGGCAGGAGAATGGTGTAAA GGCGTAGGTGGTGCACACCTGTAGTCCCAGCTGCTGGGGAGGCTGAGGCAGGAGAATGGTGTAAA T C PDCD7 Ensembl:ENSG00000090470 Protein coding 3'UTR GSE100210;GSE107867 HepG2 cell line;ASD brains,frontal_cortex - 29129909,30559470 RNA-Seq:(High) rs1357713072 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25153400 Human_miRNA_ID_501337,Human_miRNA_ID_508557,Human_miRNA_ID_830761 39078 RMVar_ID_39078 Human_SNP_ID_580899191 A-to-I Human chr15 - 65122224 65122224 65122224 TCAAGCGATTCTCCTGGCTTAGCCTCCTGAGTAGTTGGAACTACAGGCGCACGCCACCATGCTCG TCAAGCGATTCTCCTGGCTTAGCCTCCTGAGTGGTTGGAACTACAGGCGCACGCCACCATGCTCG T C PDCD7 Ensembl:ENSG00000090470 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1035044252 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70586 39079 RMVar_ID_39079 Human_SNP_ID_580899192 A-to-I Human chr15 - 65122224 65122224 65122224 TCAAGCGATTCTCCTGGCTTAGCCTCCTGAGTAGTTGGAACTACAGGCGCACGCCACCATGCTCG TCAAGCGATTCTCCTGGCTTAGCCTCCTGAGTCGTTGGAACTACAGGCGCACGCCACCATGCTCG T G PDCD7 Ensembl:ENSG00000090470 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1035044252 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70586 39080 RMVar_ID_39080 Human_SNP_ID_580901269 A-to-I Human chr15 - 65130837 65130837 65130837 GTAAGCTGAGTCTTTTTTTTTTTTTCTGAGACAGAGTCTCGCACTGTTGCCCGGACTGAAGTGCA GTAAGCTGAGTCTTTTTTTTTTTTTCTGAGACGGAGTCTCGCACTGTTGCCCGGACTGAAGTGCA T C PDCD7 Ensembl:ENSG00000090470 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053099228 Functional Loss SNV dbSNP153 33..33 33 - - - 39081 RMVar_ID_39081 Human_SNP_ID_580906445 A-to-I Human chr15 - 65149308 65149308 65149308 ACCACACCTGGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCGCCATGTTGCCCAGGCTGG ACCACACCTGGCTAATTTTTTGTATTTTTAGTGGAGACGGGGTTTCGCCATGTTGCCCAGGCTGG T C CLPX Ensembl:ENSG00000166855 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054649474 Functional Loss SNV dbSNP153 33..33 33 - - - 39082 RMVar_ID_39082 Human_SNP_ID_580906465 A-to-I Human chr15 - 65149375 65149375 65149375 TGAGTCCCAGGTTCAAGCGATACTCATGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCGTGCA TGAGTCCCAGGTTCAAGCGATACTCATGCCTCGGCCTCCTGAGTAGCTGGGACTACAGGCGTGCA T C CLPX Ensembl:ENSG00000166855 Protein coding 3'UTR GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 29129909,30559470 RNA-Seq:(High) rs1176864176 Functional Loss SNV dbSNP153 33..33 33 - - - 39083 RMVar_ID_39083 Human_SNP_ID_580906466 A-to-I Human chr15 - 65149382 65149382 65149382 CAACCTCTGAGTCCCAGGTTCAAGCGATACTCATGCCTCAGCCTCCTGAGTAGCTGGGACTACAG CAACCTCTGAGTCCCAGGTTCAAGCGATACTCGTGCCTCAGCCTCCTGAGTAGCTGGGACTACAG T C CLPX Ensembl:ENSG00000166855 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1470696597 Functional Loss SNV dbSNP153 33..33 33 - - - 39084 RMVar_ID_39084 Human_SNP_ID_580906482 A-to-I Human chr15 - 65149439 65149439 65149439 ACAGAGTCTCGCTGTGTCACCCAGGCTGGAGTACAGTGCCACAATCTTGGCTCACTGCAACCTCT ACAGAGTCTCGCTGTGTCACCCAGGCTGGAGTGCAGTGCCACAATCTTGGCTCACTGCAACCTCT T C CLPX Ensembl:ENSG00000166855 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs16948525 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8182900,Human_RBP_ID_26438167 39085 RMVar_ID_39085 Human_SNP_ID_580906495 A-to-I Human chr15 - 65149469 65149468 65149470 TATATATCTATTTTATTTTATTTTTTTGAGACAGAGTCTCGCTGTGTCACCCAGGCTGGAGTACA TATATATCTATTTTATTTTATTTTTTTGAGA__GAGTCTCGCTGTGTCACCCAGGCTGGAGTACA CTG C CLPX Ensembl:ENSG00000166855 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs922887612 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_6448568 39086 RMVar_ID_39086 Human_SNP_ID_580906496 A-to-I Human chr15 - 65149469 65149469 65149469 TATATATCTATTTTATTTTATTTTTTTGAGACAGAGTCTCGCTGTGTCACCCAGGCTGGAGTACA TATATATCTATTTTATTTTATTTTTTTGAGACGGAGTCTCGCTGTGTCACCCAGGCTGGAGTACA T C CLPX Ensembl:ENSG00000166855 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1254109553 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6448568 39087 RMVar_ID_39087 Human_SNP_ID_580906531 A-to-I Human chr15 - 65149596 65149596 65149596 CAGCCTCCCAAAGTGCTGGGATTGCAGGCGTAAGCCACCACACCCGGCCTTATTTACCATCTTTA CAGCCTCCCAAAGTGCTGGGATTGCAGGCGTAGGCCACCACACCCGGCCTTATTTACCATCTTTA T C CLPX Ensembl:ENSG00000166855 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1486562704 Functional Loss SNV dbSNP153 33..33 33 - - - 39088 RMVar_ID_39088 Human_SNP_ID_580906532 A-to-I Human chr15 - 65149597 65149597 65149597 TCAGCCTCCCAAAGTGCTGGGATTGCAGGCGTAAGCCACCACACCCGGCCTTATTTACCATCTTT TCAGCCTCCCAAAGTGCTGGGATTGCAGGCGTGAGCCACCACACCCGGCCTTATTTACCATCTTT T C CLPX Ensembl:ENSG00000166855 Protein coding 3'UTR GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 29129909,30559470 RNA-Seq:(High) rs926888702 Functional Loss SNV dbSNP153 33..33 33 - - - 39089 RMVar_ID_39089 Human_SNP_ID_580906543 A-to-I Human chr15 - 65149627 65149627 65149627 TGTAACTCCTGACCTTGTGATCTGCTGGCCTCAGCCTCCCAAAGTGCTGGGATTGCAGGCGTAAG TGTAACTCCTGACCTTGTGATCTGCTGGCCTCGGCCTCCCAAAGTGCTGGGATTGCAGGCGTAAG T C CLPX Ensembl:ENSG00000166855 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1399537862 Functional Loss SNV dbSNP153 33..33 33 - - - 39090 RMVar_ID_39090 Human_SNP_ID_580906550 A-to-I Human chr15 - 65149663 65149663 65149663 TAGAGACAGGGTTTCACCCTGTTGGCCAGGCTAGTCTGTAACTCCTGACCTTGTGATCTGCTGGC TAGAGACAGGGTTTCACCCTGTTGGCCAGGCTGGTCTGTAACTCCTGACCTTGTGATCTGCTGGC T C CLPX Ensembl:ENSG00000166855 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1376345222 Functional Loss SNV dbSNP153 33..33 33 - - - 39091 RMVar_ID_39091 Human_SNP_ID_580906557 A-to-I Human chr15 - 65149694 65149694 65149694 CACCACACCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCCTGTTGGCCAGGCTAG CACCACACCTGGCTAATTTTTGTATTTTTAGTGGAGACAGGGTTTCACCCTGTTGGCCAGGCTAG T C CLPX Ensembl:ENSG00000166855 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1429735469 Functional Loss SNV dbSNP153 33..33 33 - - - 39092 RMVar_ID_39092 Human_SNP_ID_580906575 A-to-I Human chr15 - 65149748 65149748 65149748 TCAAGCAATTTTCCTGCCTCAGCCTTCCAAGTAGCTGGGATTATAGGCACGCACCACCACACCTG TCAAGCAATTTTCCTGCCTCAGCCTTCCAAGTGGCTGGGATTATAGGCACGCACCACCACACCTG T C CLPX Ensembl:ENSG00000166855 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1396270908 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6448572 39093 RMVar_ID_39093 Human_SNP_ID_580906579 A-to-I Human chr15 - 65149774 65149774 65149774 CTCACTGCAACCTCCGCCTCCCAGGTTCAAGCAATTTTCCTGCCTCAGCCTTCCAAGTAGCTGGG CTCACTGCAACCTCCGCCTCCCAGGTTCAAGCGATTTTCCTGCCTCAGCCTTCCAAGTAGCTGGG T C CLPX Ensembl:ENSG00000166855 Protein coding 3'UTR GSE99789;GSE123020:GSM3490829,GSM3490830,GSM3490831 esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109 cell line - 29796672,32596459 RNA-Seq:(High) rs1348709643 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6448572 39094 RMVar_ID_39094 Human_SNP_ID_580906582 A-to-I Human chr15 - 65149784 65149784 65149784 GCGATCTTGGCTCACTGCAACCTCCGCCTCCCAGGTTCAAGCAATTTTCCTGCCTCAGCCTTCCA GCGATCTTGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGCAATTTTCCTGCCTCAGCCTTCCA T C CLPX Ensembl:ENSG00000166855 Protein coding 3'UTR GSE99789;GSE123020:GSM3490829,GSM3490830,GSM3490831 esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109 cell line - 29796672,32596459 RNA-Seq:(High) rs1006045359 Functional Loss SNV dbSNP153 33..33 33 - - - 39095 RMVar_ID_39095 Human_SNP_ID_580906691 A-to-I Human chr15 - 65150138 65150138 65150138 GGAGAATCGCTTGAACTCGGAGGGCAGAGTTTACAGTGAGCTGAGGTTGTGCCACTGCACTCCAG GGAGAATCGCTTGAACTCGGAGGGCAGAGTTTGCAGTGAGCTGAGGTTGTGCCACTGCACTCCAG T C CLPX Ensembl:ENSG00000166855 Protein coding 3'UTR GSE38233;GSE112787;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;293 Flip-In T-REx cells,empty vector;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29967493,31158229,31158229 RNA-Seq:(High) rs1354359084 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26435173 RMVar_hsa_circ_173103 39096 RMVar_ID_39096 Human_SNP_ID_580906693 A-to-I Human chr15 - 65150145 65150145 65150145 TGAGGCAGGAGAATCGCTTGAACTCGGAGGGCAGAGTTTACAGTGAGCTGAGGTTGTGCCACTGC TGAGGCAGGAGAATCGCTTGAACTCGGAGGGCGGAGTTTACAGTGAGCTGAGGTTGTGCCACTGC T C CLPX Ensembl:ENSG00000166855 Protein coding 3'UTR GSE38233;GSE99789;GSE112787;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;esophageal squamous carcinoma cells,EC109;293 Flip-In T-REx cells,empty vector;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29796672,29967493,32596459 RNA-Seq:(High) rs1416346281 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26435173 39097 RMVar_ID_39097 Human_SNP_ID_580906708 A-to-I Human chr15 - 65150197 65150197 65150197 AAATTAGCTGGGTGCCGTGGCAGGTGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAA AAATTAGCTGGGTGCCGTGGCAGGTGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAA T C CLPX Ensembl:ENSG00000166855 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1211214217 Functional Loss SNV dbSNP153 33..33 33 - - - 39098 RMVar_ID_39098 Human_SNP_ID_580906709 A-to-I Human chr15 - 65150198 65150198 65150198 AAAATTAGCTGGGTGCCGTGGCAGGTGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTAGCTGGGTGCCGTGGCAGGTGCCTGTTATCCCAGCTACTCGGGAGGCTGAGGCAGGAGA T A CLPX Ensembl:ENSG00000166855 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1316381518 Functional Loss SNV dbSNP153 33..33 33 - - - 39099 RMVar_ID_39099 Human_SNP_ID_580906710 A-to-I Human chr15 - 65150198 65150198 65150198 AAAATTAGCTGGGTGCCGTGGCAGGTGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTAGCTGGGTGCCGTGGCAGGTGCCTGTGATCCCAGCTACTCGGGAGGCTGAGGCAGGAGA T C CLPX Ensembl:ENSG00000166855 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1316381518 Functional Loss SNV dbSNP153 33..33 33 - - - 39100 RMVar_ID_39100 Human_SNP_ID_580906722 A-to-I Human chr15 - 65150237 65150235 65150238 GGCCAAGATGGTGAAACCCCATCTCTACTAAAAATATGAAAAATTAGCTGGGTGCCGTGGCAGGT GGCCAAGATGGTGAAACCCCATCTCTACTAA___TATGAAAAATTAGCTGGGTGCCGTGGCAGGT ATTT A CLPX Ensembl:ENSG00000166855 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1407269636 Functional Loss DEL dbSNP153 32..34 33 - - - 39101 RMVar_ID_39101 Human_SNP_ID_580906725 A-to-I Human chr15 - 65150240 65150240 65150240 CCTGGCCAAGATGGTGAAACCCCATCTCTACTAAAAATATGAAAAATTAGCTGGGTGCCGTGGCA CCTGGCCAAGATGGTGAAACCCCATCTCTACTGAAAATATGAAAAATTAGCTGGGTGCCGTGGCA T C CLPX Ensembl:ENSG00000166855 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1470725297 Functional Loss SNV dbSNP153 33..33 33 - - - 39102 RMVar_ID_39102 Human_SNP_ID_580906726 A-to-I Human chr15 - 65150243 65150243 65150243 CAGCCTGGCCAAGATGGTGAAACCCCATCTCTACTAAAAATATGAAAAATTAGCTGGGTGCCGTG CAGCCTGGCCAAGATGGTGAAACCCCATCTCTGCTAAAAATATGAAAAATTAGCTGGGTGCCGTG T C CLPX Ensembl:ENSG00000166855 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1240516711 Functional Loss SNV dbSNP153 33..33 33 - - - 39103 RMVar_ID_39103 Human_SNP_ID_580906728 A-to-I Human chr15 - 65150249 65150249 65150249 CAAGACCAGCCTGGCCAAGATGGTGAAACCCCATCTCTACTAAAAATATGAAAAATTAGCTGGGT CAAGACCAGCCTGGCCAAGATGGTGAAACCCCGTCTCTACTAAAAATATGAAAAATTAGCTGGGT T C CLPX Ensembl:ENSG00000166855 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1011071261 Functional Loss SNV dbSNP153 33..33 33 - - - 39104 RMVar_ID_39104 Human_SNP_ID_580906729 A-to-I Human chr15 - 65150254 65150253 65150254 GAGTTCAAGACCAGCCTGGCCAAGATGGTGAAACCCCATCTCTACTAAAAATATGAAAAATTAGC GAGTTCAAGACCAGCCTGGCCAAGATGGTGAA_CCCCATCTCTACTAAAAATATGAAAAATTAGC GT G CLPX Ensembl:ENSG00000166855 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1223208906 Functional Loss DEL dbSNP153 33..33 33 - - - 39105 RMVar_ID_39105 Human_SNP_ID_580906743 A-to-I Human chr15 - 65150310 65150310 65150310 TCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGTGGATCACGAGGTCAGGAGTTCAAG TCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGTGGATCACGAGGTCAGGAGTTCAAG T C CLPX Ensembl:ENSG00000166855 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs184037264 Functional Loss SNV dbSNP153 33..33 33 - - - 39106 RMVar_ID_39106 Human_SNP_ID_580911747 A-to-I Human chr15 - 65169889 65169889 65169889 GGGCGTGGTGACACATGCCTGTAATCCCAGCTACTTCGGAGGCTGAGGCAAGAGAATTGCTTGAA GGGCGTGGTGACACATGCCTGTAATCCCAGCTTCTTCGGAGGCTGAGGCAAGAGAATTGCTTGAA T A CLPX Ensembl:ENSG00000166855 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1450364187 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118912,RMVar_hsa_circ_173108,RMVar_hsa_circ_357325,RMVar_hsa_circ_334752,RMVar_hsa_circ_173112,RMVar_hsa_circ_173113,RMVar_hsa_circ_336378,RMVar_hsa_circ_361353,RMVar_hsa_circ_98363 39107 RMVar_ID_39107 Human_SNP_ID_580911748 A-to-I Human chr15 - 65169889 65169889 65169889 GGGCGTGGTGACACATGCCTGTAATCCCAGCTACTTCGGAGGCTGAGGCAAGAGAATTGCTTGAA GGGCGTGGTGACACATGCCTGTAATCCCAGCTGCTTCGGAGGCTGAGGCAAGAGAATTGCTTGAA T C CLPX Ensembl:ENSG00000166855 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1450364187 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118912,RMVar_hsa_circ_173108,RMVar_hsa_circ_357325,RMVar_hsa_circ_334752,RMVar_hsa_circ_173112,RMVar_hsa_circ_173113,RMVar_hsa_circ_336378,RMVar_hsa_circ_361353,RMVar_hsa_circ_98363 39108 RMVar_ID_39108 Human_SNP_ID_580914273 A-to-I Human chr15 - 65180112 65180112 65180112 AGATTCTGCAAAGAGCTCCTCTTAGATCCTTTACAGAAACACCAGCATACTTTGCCTCAAAAGAT AGATTCTGCAAAGAGCTCCTCTTAGATCCTTTGCAGAAACACCAGCATACTTTGCCTCAAAAGAT T C CLPX Ensembl:ENSG00000166855 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1311098218 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1614046,Human_Splice_Rec_1614047,Human_Splice_Rec_1614072,Human_Splice_Rec_1614073,Human_Splice_Rec_1614100,Human_Splice_Rec_1614101,Human_Splice_Rec_1614118,Human_Splice_Rec_1614119 RMVar_hsa_circ_118912,RMVar_hsa_circ_173108,RMVar_hsa_circ_357325,RMVar_hsa_circ_334752,RMVar_hsa_circ_173112,RMVar_hsa_circ_173114,RMVar_hsa_circ_336378,RMVar_hsa_circ_361353,RMVar_hsa_circ_173115,RMVar_hsa_circ_270461 39109 RMVar_ID_39109 Human_SNP_ID_580987380 A-to-I Human chr15 - 65444347 65444347 65444347 GTTTTTAAAGACTTGATAAATGTGTACACTTGAACAACCATCCAGAGGGATAGTTACTTGAGCAT GTTTTTAAAGACTTGATAAATGTGTACACTTGTACAACCATCCAGAGGGATAGTTACTTGAGCAT T A DPP8 Ensembl:ENSG00000074603 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1487819087 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3479247,Human_RBP_ID_6448826,Human_RBP_ID_12556329,Human_RBP_ID_23660793 39110 RMVar_ID_39110 Human_SNP_ID_580988251 A-to-I Human chr15 - 65448331 65448331 65448331 ATGGGTGTCACTAAGTTGCCCAGGCTGATCTCAAACTCCTGAACTCAAGCGATCCTCCCACCTGA ATGGGTGTCACTAAGTTGCCCAGGCTGATCTCCAACTCCTGAACTCAAGCGATCCTCCCACCTGA T G DPP8 Ensembl:ENSG00000074603 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs949120184 Functional Loss SNV dbSNP153 33..33 33 - - - 39111 RMVar_ID_39111 Human_SNP_ID_580991384 A-to-I Human chr15 - 65460412 65460412 65460412 TTTTGAGACAGTCTCGCTCTGTCTTCCAGGCTATAATGCAGAGGCATGATCTCAGCTCACTGCCT TTTTGAGACAGTCTCGCTCTGTCTTCCAGGCTGTAATGCAGAGGCATGATCTCAGCTCACTGCCT T C DPP8 Ensembl:ENSG00000074603 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs994697785 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_173141,RMVar_hsa_circ_13426,RMVar_hsa_circ_357736,RMVar_hsa_circ_320708,RMVar_hsa_circ_336881,RMVar_hsa_circ_302658,RMVar_hsa_circ_70692,RMVar_hsa_circ_112272,RMVar_hsa_circ_173137,RMVar_hsa_circ_173139,RMVar_hsa_circ_173140,RMVar_hsa_circ_173138,RMVar_hsa_circ_331946,RMVar_hsa_circ_52689,RMVar_hsa_circ_24960,RMVar_hsa_circ_18846,RMVar_hsa_circ_173143,RMVar_hsa_circ_279543,RMVar_hsa_circ_310099,RMVar_hsa_circ_320649,RMVar_hsa_circ_327338,RMVar_hsa_circ_300377,RMVar_hsa_circ_279742,RMVar_hsa_circ_173145,RMVar_hsa_circ_173144,RMVar_hsa_circ_64967,RMVar_hsa_circ_173142,RMVar_hsa_circ_368648,RMVar_hsa_circ_61619,RMVar_hsa_circ_45117,RMVar_hsa_circ_41156,RMVar_hsa_circ_173147,RMVar_hsa_circ_364428,RMVar_hsa_circ_173148,RMVar_hsa_circ_102378,RMVar_hsa_circ_173149 39112 RMVar_ID_39112 Human_SNP_ID_580994091 A-to-I Human chr15 - 65470530 65470530 65470530 GCGATGTTGGCTCACTGTAACCTCTGCCTCCCAGGTTCAAGCAATTCTCCTGCCTCAGCCCCCTG GCGATGTTGGCTCACTGTAACCTCTGCCTCCCGGGTTCAAGCAATTCTCCTGCCTCAGCCCCCTG T C DPP8 Ensembl:ENSG00000074603 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1193435993 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_215,RMVar_hsa_circ_173141,RMVar_hsa_circ_13426,RMVar_hsa_circ_357736,RMVar_hsa_circ_320708,RMVar_hsa_circ_336881,RMVar_hsa_circ_302658,RMVar_hsa_circ_112272,RMVar_hsa_circ_173137,RMVar_hsa_circ_173139,RMVar_hsa_circ_173140,RMVar_hsa_circ_173138,RMVar_hsa_circ_331946,RMVar_hsa_circ_52689,RMVar_hsa_circ_18846,RMVar_hsa_circ_173143,RMVar_hsa_circ_279543,RMVar_hsa_circ_310099,RMVar_hsa_circ_320649,RMVar_hsa_circ_300377,RMVar_hsa_circ_173145,RMVar_hsa_circ_173144,RMVar_hsa_circ_173142,RMVar_hsa_circ_368648,RMVar_hsa_circ_61619,RMVar_hsa_circ_45117,RMVar_hsa_circ_41156,RMVar_hsa_circ_173147,RMVar_hsa_circ_364428,RMVar_hsa_circ_173148,RMVar_hsa_circ_102378,RMVar_hsa_circ_284795,RMVar_hsa_circ_297454,RMVar_hsa_circ_316014,RMVar_hsa_circ_173149,RMVar_hsa_circ_339635,RMVar_hsa_circ_309179,RMVar_hsa_circ_294412,RMVar_hsa_circ_294122,RMVar_hsa_circ_280242,RMVar_hsa_circ_282712,RMVar_hsa_circ_52669,RMVar_hsa_circ_66108,RMVar_hsa_circ_173153,RMVar_hsa_circ_173155,RMVar_hsa_circ_173156,RMVar_hsa_circ_173154,RMVar_hsa_circ_364412,RMVar_hsa_circ_173151,RMVar_hsa_circ_173152,RMVar_hsa_circ_173150,RMVar_hsa_circ_366503,RMVar_hsa_circ_308153,RMVar_hsa_circ_275394,RMVar_hsa_circ_173160,RMVar_hsa_circ_42342,RMVar_hsa_circ_42800,RMVar_hsa_circ_26411,RMVar_hsa_circ_173161,RMVar_hsa_circ_173159,RMVar_hsa_circ_127562,RMVar_hsa_circ_173162 39113 RMVar_ID_39113 Human_SNP_ID_580994575 A-to-I Human chr15 - 65472450 65472450 65472450 CCAAAAATAAAAAATAAAAAAATTAGCTGGGCATGGTGATGCGCACCTGTAGTCCCAGCTAGTTG CCAAAAATAAAAAATAAAAAAATTAGCTGGGCGTGGTGATGCGCACCTGTAGTCCCAGCTAGTTG T C DPP8 Ensembl:ENSG00000074603 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs954218390 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_215,RMVar_hsa_circ_173141,RMVar_hsa_circ_13426,RMVar_hsa_circ_357736,RMVar_hsa_circ_320708,RMVar_hsa_circ_336881,RMVar_hsa_circ_302658,RMVar_hsa_circ_112272,RMVar_hsa_circ_173137,RMVar_hsa_circ_173139,RMVar_hsa_circ_173140,RMVar_hsa_circ_173138,RMVar_hsa_circ_331946,RMVar_hsa_circ_52689,RMVar_hsa_circ_18846,RMVar_hsa_circ_173143,RMVar_hsa_circ_279543,RMVar_hsa_circ_310099,RMVar_hsa_circ_320649,RMVar_hsa_circ_300377,RMVar_hsa_circ_173145,RMVar_hsa_circ_173144,RMVar_hsa_circ_173142,RMVar_hsa_circ_368648,RMVar_hsa_circ_61619,RMVar_hsa_circ_45117,RMVar_hsa_circ_41156,RMVar_hsa_circ_173147,RMVar_hsa_circ_364428,RMVar_hsa_circ_173148,RMVar_hsa_circ_102378,RMVar_hsa_circ_284795,RMVar_hsa_circ_297454,RMVar_hsa_circ_316014,RMVar_hsa_circ_173149,RMVar_hsa_circ_339635,RMVar_hsa_circ_309179,RMVar_hsa_circ_294412,RMVar_hsa_circ_294122,RMVar_hsa_circ_280242,RMVar_hsa_circ_282712,RMVar_hsa_circ_52669,RMVar_hsa_circ_66108,RMVar_hsa_circ_173153,RMVar_hsa_circ_173155,RMVar_hsa_circ_173156,RMVar_hsa_circ_173154,RMVar_hsa_circ_364412,RMVar_hsa_circ_173151,RMVar_hsa_circ_173152,RMVar_hsa_circ_173150,RMVar_hsa_circ_366503,RMVar_hsa_circ_308153,RMVar_hsa_circ_275394,RMVar_hsa_circ_173160,RMVar_hsa_circ_42342,RMVar_hsa_circ_42800,RMVar_hsa_circ_26411,RMVar_hsa_circ_173161,RMVar_hsa_circ_173159,RMVar_hsa_circ_127562,RMVar_hsa_circ_173162 39114 RMVar_ID_39114 Human_SNP_ID_580994597 A-to-I Human chr15 - 65472526 65472525 65472526 GGAGATGAAGGCTGGAGAATCGCTTGAGGCCAAGAGTTCAGTAACAGTTTGGGCAACATATAAGA GGAGATGAAGGCTGGAGAATCGCTTGAGGCCA_GAGTTCAGTAACAGTTTGGGCAACATATAAGA CT C DPP8 Ensembl:ENSG00000074603 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1393255352 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_6448965,Human_RBP_ID_8420447,Human_RBP_ID_12556578 RMVar_hsa_circ_215,RMVar_hsa_circ_173141,RMVar_hsa_circ_13426,RMVar_hsa_circ_357736,RMVar_hsa_circ_320708,RMVar_hsa_circ_336881,RMVar_hsa_circ_302658,RMVar_hsa_circ_112272,RMVar_hsa_circ_173137,RMVar_hsa_circ_173139,RMVar_hsa_circ_173140,RMVar_hsa_circ_173138,RMVar_hsa_circ_331946,RMVar_hsa_circ_52689,RMVar_hsa_circ_18846,RMVar_hsa_circ_173143,RMVar_hsa_circ_279543,RMVar_hsa_circ_310099,RMVar_hsa_circ_320649,RMVar_hsa_circ_300377,RMVar_hsa_circ_173145,RMVar_hsa_circ_173144,RMVar_hsa_circ_173142,RMVar_hsa_circ_368648,RMVar_hsa_circ_61619,RMVar_hsa_circ_45117,RMVar_hsa_circ_41156,RMVar_hsa_circ_173147,RMVar_hsa_circ_364428,RMVar_hsa_circ_173148,RMVar_hsa_circ_102378,RMVar_hsa_circ_284795,RMVar_hsa_circ_297454,RMVar_hsa_circ_316014,RMVar_hsa_circ_173149,RMVar_hsa_circ_339635,RMVar_hsa_circ_309179,RMVar_hsa_circ_294412,RMVar_hsa_circ_294122,RMVar_hsa_circ_280242,RMVar_hsa_circ_282712,RMVar_hsa_circ_52669,RMVar_hsa_circ_66108,RMVar_hsa_circ_173153,RMVar_hsa_circ_173155,RMVar_hsa_circ_173156,RMVar_hsa_circ_173154,RMVar_hsa_circ_364412,RMVar_hsa_circ_173151,RMVar_hsa_circ_173152,RMVar_hsa_circ_173150,RMVar_hsa_circ_366503,RMVar_hsa_circ_308153,RMVar_hsa_circ_275394,RMVar_hsa_circ_173160,RMVar_hsa_circ_42342,RMVar_hsa_circ_42800,RMVar_hsa_circ_26411,RMVar_hsa_circ_173161,RMVar_hsa_circ_173159,RMVar_hsa_circ_127562,RMVar_hsa_circ_173162 39115 RMVar_ID_39115 Human_SNP_ID_580997205 A-to-I Human chr15 - 65482171 65482171 65482171 TTAATTTCATTACAAGCACACACCTTACCTGTAGTCTCAGCTACTCAGGAGGCTGAGGCAGGAGG TTAATTTCATTACAAGCACACACCTTACCTGTGGTCTCAGCTACTCAGGAGGCTGAGGCAGGAGG T C DPP8 Ensembl:ENSG00000074603 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1022373277 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_173141,RMVar_hsa_circ_357736,RMVar_hsa_circ_336881,RMVar_hsa_circ_112272,RMVar_hsa_circ_173139,RMVar_hsa_circ_173140,RMVar_hsa_circ_331946,RMVar_hsa_circ_279543,RMVar_hsa_circ_173142,RMVar_hsa_circ_45117,RMVar_hsa_circ_364428,RMVar_hsa_circ_102378,RMVar_hsa_circ_316014,RMVar_hsa_circ_173149,RMVar_hsa_circ_309179,RMVar_hsa_circ_294122,RMVar_hsa_circ_280242,RMVar_hsa_circ_282712,RMVar_hsa_circ_52669,RMVar_hsa_circ_66108,RMVar_hsa_circ_173151,RMVar_hsa_circ_173152,RMVar_hsa_circ_173150,RMVar_hsa_circ_366503,RMVar_hsa_circ_42342,RMVar_hsa_circ_42800,RMVar_hsa_circ_26411,RMVar_hsa_circ_173161,RMVar_hsa_circ_805,RMVar_hsa_circ_285487,RMVar_hsa_circ_173163,RMVar_hsa_circ_358449,RMVar_hsa_circ_362238,RMVar_hsa_circ_321862,RMVar_hsa_circ_29364,RMVar_hsa_circ_279944,RMVar_hsa_circ_314344,RMVar_hsa_circ_335404,RMVar_hsa_circ_173164,RMVar_hsa_circ_329550,RMVar_hsa_circ_286130,RMVar_hsa_circ_54421,RMVar_hsa_circ_173169,RMVar_hsa_circ_67906,RMVar_hsa_circ_282720,RMVar_hsa_circ_36448,RMVar_hsa_circ_173173,RMVar_hsa_circ_283025,RMVar_hsa_circ_173171,RMVar_hsa_circ_307832,RMVar_hsa_circ_339218,RMVar_hsa_circ_353186,RMVar_hsa_circ_298216,RMVar_hsa_circ_173175,RMVar_hsa_circ_126780,RMVar_hsa_circ_173174,RMVar_hsa_circ_173172 39116 RMVar_ID_39116 Human_SNP_ID_580997303 A-to-I Human chr15 - 65482571 65482571 65482571 ACTATTTCTTTAGTATATTACACAAATGGGCCAAGCACGGTGGCTTACACCTGTAATCCCAACTA ACTATTTCTTTAGTATATTACACAAATGGGCCGAGCACGGTGGCTTACACCTGTAATCCCAACTA T C DPP8 Ensembl:ENSG00000074603 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1203859089 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6448995 RMVar_hsa_circ_173141,RMVar_hsa_circ_357736,RMVar_hsa_circ_336881,RMVar_hsa_circ_112272,RMVar_hsa_circ_173139,RMVar_hsa_circ_173140,RMVar_hsa_circ_331946,RMVar_hsa_circ_279543,RMVar_hsa_circ_173142,RMVar_hsa_circ_45117,RMVar_hsa_circ_364428,RMVar_hsa_circ_102378,RMVar_hsa_circ_316014,RMVar_hsa_circ_173149,RMVar_hsa_circ_309179,RMVar_hsa_circ_294122,RMVar_hsa_circ_280242,RMVar_hsa_circ_282712,RMVar_hsa_circ_52669,RMVar_hsa_circ_66108,RMVar_hsa_circ_173151,RMVar_hsa_circ_173152,RMVar_hsa_circ_173150,RMVar_hsa_circ_366503,RMVar_hsa_circ_42342,RMVar_hsa_circ_42800,RMVar_hsa_circ_26411,RMVar_hsa_circ_173161,RMVar_hsa_circ_805,RMVar_hsa_circ_285487,RMVar_hsa_circ_173163,RMVar_hsa_circ_358449,RMVar_hsa_circ_362238,RMVar_hsa_circ_321862,RMVar_hsa_circ_29364,RMVar_hsa_circ_279944,RMVar_hsa_circ_314344,RMVar_hsa_circ_335404,RMVar_hsa_circ_173164,RMVar_hsa_circ_329550,RMVar_hsa_circ_286130,RMVar_hsa_circ_54421,RMVar_hsa_circ_173169,RMVar_hsa_circ_67906,RMVar_hsa_circ_282720,RMVar_hsa_circ_36448,RMVar_hsa_circ_173173,RMVar_hsa_circ_283025,RMVar_hsa_circ_173171,RMVar_hsa_circ_307832,RMVar_hsa_circ_339218,RMVar_hsa_circ_353186,RMVar_hsa_circ_298216,RMVar_hsa_circ_173175,RMVar_hsa_circ_126780,RMVar_hsa_circ_173174,RMVar_hsa_circ_173172 39117 RMVar_ID_39117 Human_SNP_ID_580997509 A-to-I Human chr15 - 65483414 65483414 65483414 AGGCTCAAGTGATCCTCCTGCCTCCGCCTTCTAAGTAGCTGGGACCACAGGCACACACCACCATG AGGCTCAAGTGATCCTCCTGCCTCCGCCTTCTGAGTAGCTGGGACCACAGGCACACACCACCATG T C DPP8 Ensembl:ENSG00000074603 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs942095181 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_173141,RMVar_hsa_circ_357736,RMVar_hsa_circ_336881,RMVar_hsa_circ_112272,RMVar_hsa_circ_173139,RMVar_hsa_circ_173140,RMVar_hsa_circ_331946,RMVar_hsa_circ_279543,RMVar_hsa_circ_173142,RMVar_hsa_circ_45117,RMVar_hsa_circ_364428,RMVar_hsa_circ_102378,RMVar_hsa_circ_316014,RMVar_hsa_circ_173149,RMVar_hsa_circ_309179,RMVar_hsa_circ_294122,RMVar_hsa_circ_280242,RMVar_hsa_circ_282712,RMVar_hsa_circ_52669,RMVar_hsa_circ_66108,RMVar_hsa_circ_173151,RMVar_hsa_circ_173152,RMVar_hsa_circ_173150,RMVar_hsa_circ_366503,RMVar_hsa_circ_42342,RMVar_hsa_circ_42800,RMVar_hsa_circ_26411,RMVar_hsa_circ_173161,RMVar_hsa_circ_805,RMVar_hsa_circ_285487,RMVar_hsa_circ_173163,RMVar_hsa_circ_358449,RMVar_hsa_circ_362238,RMVar_hsa_circ_321862,RMVar_hsa_circ_29364,RMVar_hsa_circ_279944,RMVar_hsa_circ_314344,RMVar_hsa_circ_335404,RMVar_hsa_circ_173164,RMVar_hsa_circ_329550,RMVar_hsa_circ_286130,RMVar_hsa_circ_54421,RMVar_hsa_circ_173169,RMVar_hsa_circ_67906,RMVar_hsa_circ_282720,RMVar_hsa_circ_36448,RMVar_hsa_circ_173173,RMVar_hsa_circ_283025,RMVar_hsa_circ_173171,RMVar_hsa_circ_307832,RMVar_hsa_circ_339218,RMVar_hsa_circ_353186,RMVar_hsa_circ_298216,RMVar_hsa_circ_173175,RMVar_hsa_circ_126780,RMVar_hsa_circ_173174,RMVar_hsa_circ_173172 39118 RMVar_ID_39118 Human_SNP_ID_580998670 A-to-I Human chr15 - 65487435 65487435 65487435 GAATTAGAAGGTATCTTTGCGCCGGGCGTGGTAGCTCACGTCTGTAATCTCAGCACTTTGGGAAG GAATTAGAAGGTATCTTTGCGCCGGGCGTGGTTGCTCACGTCTGTAATCTCAGCACTTTGGGAAG T A DPP8 Ensembl:ENSG00000074603 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042761080 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_173141,RMVar_hsa_circ_336881,RMVar_hsa_circ_112272,RMVar_hsa_circ_173139,RMVar_hsa_circ_173140,RMVar_hsa_circ_331946,RMVar_hsa_circ_279543,RMVar_hsa_circ_173142,RMVar_hsa_circ_45117,RMVar_hsa_circ_364428,RMVar_hsa_circ_102378,RMVar_hsa_circ_316014,RMVar_hsa_circ_173149,RMVar_hsa_circ_294122,RMVar_hsa_circ_280242,RMVar_hsa_circ_282712,RMVar_hsa_circ_52669,RMVar_hsa_circ_66108,RMVar_hsa_circ_173151,RMVar_hsa_circ_173150,RMVar_hsa_circ_42342,RMVar_hsa_circ_42800,RMVar_hsa_circ_26411,RMVar_hsa_circ_173161,RMVar_hsa_circ_805,RMVar_hsa_circ_285487,RMVar_hsa_circ_173163,RMVar_hsa_circ_358449,RMVar_hsa_circ_362238,RMVar_hsa_circ_321862,RMVar_hsa_circ_29364,RMVar_hsa_circ_314344,RMVar_hsa_circ_335404,RMVar_hsa_circ_173164,RMVar_hsa_circ_329550,RMVar_hsa_circ_54421,RMVar_hsa_circ_67906,RMVar_hsa_circ_282720,RMVar_hsa_circ_36448,RMVar_hsa_circ_35719,RMVar_hsa_circ_173173,RMVar_hsa_circ_283025,RMVar_hsa_circ_173171,RMVar_hsa_circ_307832,RMVar_hsa_circ_339218,RMVar_hsa_circ_298216,RMVar_hsa_circ_173175,RMVar_hsa_circ_126780,RMVar_hsa_circ_173174,RMVar_hsa_circ_65288,RMVar_hsa_circ_293664,RMVar_hsa_circ_173172,RMVar_hsa_circ_278237,RMVar_hsa_circ_59905,RMVar_hsa_circ_173177,RMVar_hsa_circ_14268,RMVar_hsa_circ_173176 39119 RMVar_ID_39119 Human_SNP_ID_580998671 A-to-I Human chr15 - 65487435 65487435 65487435 GAATTAGAAGGTATCTTTGCGCCGGGCGTGGTAGCTCACGTCTGTAATCTCAGCACTTTGGGAAG GAATTAGAAGGTATCTTTGCGCCGGGCGTGGTGGCTCACGTCTGTAATCTCAGCACTTTGGGAAG T C DPP8 Ensembl:ENSG00000074603 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042761080 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_173141,RMVar_hsa_circ_336881,RMVar_hsa_circ_112272,RMVar_hsa_circ_173139,RMVar_hsa_circ_173140,RMVar_hsa_circ_331946,RMVar_hsa_circ_279543,RMVar_hsa_circ_173142,RMVar_hsa_circ_45117,RMVar_hsa_circ_364428,RMVar_hsa_circ_102378,RMVar_hsa_circ_316014,RMVar_hsa_circ_173149,RMVar_hsa_circ_294122,RMVar_hsa_circ_280242,RMVar_hsa_circ_282712,RMVar_hsa_circ_52669,RMVar_hsa_circ_66108,RMVar_hsa_circ_173151,RMVar_hsa_circ_173150,RMVar_hsa_circ_42342,RMVar_hsa_circ_42800,RMVar_hsa_circ_26411,RMVar_hsa_circ_173161,RMVar_hsa_circ_805,RMVar_hsa_circ_285487,RMVar_hsa_circ_173163,RMVar_hsa_circ_358449,RMVar_hsa_circ_362238,RMVar_hsa_circ_321862,RMVar_hsa_circ_29364,RMVar_hsa_circ_314344,RMVar_hsa_circ_335404,RMVar_hsa_circ_173164,RMVar_hsa_circ_329550,RMVar_hsa_circ_54421,RMVar_hsa_circ_67906,RMVar_hsa_circ_282720,RMVar_hsa_circ_36448,RMVar_hsa_circ_35719,RMVar_hsa_circ_173173,RMVar_hsa_circ_283025,RMVar_hsa_circ_173171,RMVar_hsa_circ_307832,RMVar_hsa_circ_339218,RMVar_hsa_circ_298216,RMVar_hsa_circ_173175,RMVar_hsa_circ_126780,RMVar_hsa_circ_173174,RMVar_hsa_circ_65288,RMVar_hsa_circ_293664,RMVar_hsa_circ_173172,RMVar_hsa_circ_278237,RMVar_hsa_circ_59905,RMVar_hsa_circ_173177,RMVar_hsa_circ_14268,RMVar_hsa_circ_173176 39120 RMVar_ID_39120 Human_SNP_ID_581000018 A-to-I Human chr15 - 65492185 65492185 65492185 GGCACCTGCCATCACACCTGGCTAAATTTTGTATTTTTTGTAGAGGCGGGGTTTCACTATGTTGC GGCACCTGCCATCACACCTGGCTAAATTTTGTGTTTTTTGTAGAGGCGGGGTTTCACTATGTTGC T C DPP8 Ensembl:ENSG00000074603 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1567242579 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_173141,RMVar_hsa_circ_336881,RMVar_hsa_circ_112272,RMVar_hsa_circ_173139,RMVar_hsa_circ_173140,RMVar_hsa_circ_331946,RMVar_hsa_circ_279543,RMVar_hsa_circ_173142,RMVar_hsa_circ_45117,RMVar_hsa_circ_364428,RMVar_hsa_circ_102378,RMVar_hsa_circ_316014,RMVar_hsa_circ_173149,RMVar_hsa_circ_294122,RMVar_hsa_circ_282712,RMVar_hsa_circ_66108,RMVar_hsa_circ_173150,RMVar_hsa_circ_42800,RMVar_hsa_circ_26411,RMVar_hsa_circ_173161,RMVar_hsa_circ_173179,RMVar_hsa_circ_805,RMVar_hsa_circ_285487,RMVar_hsa_circ_173163,RMVar_hsa_circ_358449,RMVar_hsa_circ_362238,RMVar_hsa_circ_314344,RMVar_hsa_circ_173164,RMVar_hsa_circ_329550,RMVar_hsa_circ_54421,RMVar_hsa_circ_67906,RMVar_hsa_circ_282720,RMVar_hsa_circ_36448,RMVar_hsa_circ_173173,RMVar_hsa_circ_173171,RMVar_hsa_circ_339218,RMVar_hsa_circ_298216,RMVar_hsa_circ_126780,RMVar_hsa_circ_65288,RMVar_hsa_circ_173172,RMVar_hsa_circ_278237,RMVar_hsa_circ_59905,RMVar_hsa_circ_292792,RMVar_hsa_circ_173177,RMVar_hsa_circ_14268,RMVar_hsa_circ_321021,RMVar_hsa_circ_356719,RMVar_hsa_circ_348803,RMVar_hsa_circ_298421,RMVar_hsa_circ_110309,RMVar_hsa_circ_173180,RMVar_hsa_circ_173181,RMVar_hsa_circ_173183,RMVar_hsa_circ_173185,RMVar_hsa_circ_304187,RMVar_hsa_circ_336927,RMVar_hsa_circ_173178,RMVar_hsa_circ_329167,RMVar_hsa_circ_282183,RMVar_hsa_circ_173184,RMVar_hsa_circ_173182 39121 RMVar_ID_39121 Human_SNP_ID_581000024 A-to-I Human chr15 - 65492230 65492230 65492230 TCAAGTGATTCTCCTACCTCAGCCTCCCGAGTAACTGGGACCATAGGCACCTGCCATCACACCTG TCAAGTGATTCTCCTACCTCAGCCTCCCGAGTTACTGGGACCATAGGCACCTGCCATCACACCTG T A DPP8 Ensembl:ENSG00000074603 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1340690326 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_173141,RMVar_hsa_circ_336881,RMVar_hsa_circ_112272,RMVar_hsa_circ_173139,RMVar_hsa_circ_173140,RMVar_hsa_circ_331946,RMVar_hsa_circ_279543,RMVar_hsa_circ_173142,RMVar_hsa_circ_45117,RMVar_hsa_circ_364428,RMVar_hsa_circ_102378,RMVar_hsa_circ_316014,RMVar_hsa_circ_173149,RMVar_hsa_circ_294122,RMVar_hsa_circ_282712,RMVar_hsa_circ_66108,RMVar_hsa_circ_173150,RMVar_hsa_circ_42800,RMVar_hsa_circ_26411,RMVar_hsa_circ_173161,RMVar_hsa_circ_173179,RMVar_hsa_circ_805,RMVar_hsa_circ_285487,RMVar_hsa_circ_173163,RMVar_hsa_circ_358449,RMVar_hsa_circ_362238,RMVar_hsa_circ_314344,RMVar_hsa_circ_173164,RMVar_hsa_circ_329550,RMVar_hsa_circ_54421,RMVar_hsa_circ_67906,RMVar_hsa_circ_282720,RMVar_hsa_circ_36448,RMVar_hsa_circ_173173,RMVar_hsa_circ_173171,RMVar_hsa_circ_339218,RMVar_hsa_circ_298216,RMVar_hsa_circ_126780,RMVar_hsa_circ_65288,RMVar_hsa_circ_173172,RMVar_hsa_circ_278237,RMVar_hsa_circ_59905,RMVar_hsa_circ_292792,RMVar_hsa_circ_173177,RMVar_hsa_circ_14268,RMVar_hsa_circ_321021,RMVar_hsa_circ_356719,RMVar_hsa_circ_348803,RMVar_hsa_circ_298421,RMVar_hsa_circ_110309,RMVar_hsa_circ_173180,RMVar_hsa_circ_173181,RMVar_hsa_circ_173183,RMVar_hsa_circ_173185,RMVar_hsa_circ_304187,RMVar_hsa_circ_336927,RMVar_hsa_circ_173178,RMVar_hsa_circ_329167,RMVar_hsa_circ_282183,RMVar_hsa_circ_173184,RMVar_hsa_circ_173182 39122 RMVar_ID_39122 Human_SNP_ID_581000250 A-to-I Human chr15 - 65493082 65493080 65493082 CAAAACTCCGTCTAAAAAAAAAGAGAGAAAGAAAGAAAACAGAAAAGGAAAGAAAAGAAAGAAAA CAAAACTCCGTCTAAAAAAAAAGAGAGAAAGA__GAAAACAGAAAAGGAAAGAAAAGAAAGAAAA CTT C DPP8 Ensembl:ENSG00000074603 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs774662114 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_173141,RMVar_hsa_circ_336881,RMVar_hsa_circ_112272,RMVar_hsa_circ_173139,RMVar_hsa_circ_173140,RMVar_hsa_circ_331946,RMVar_hsa_circ_279543,RMVar_hsa_circ_173142,RMVar_hsa_circ_45117,RMVar_hsa_circ_364428,RMVar_hsa_circ_102378,RMVar_hsa_circ_316014,RMVar_hsa_circ_173149,RMVar_hsa_circ_294122,RMVar_hsa_circ_282712,RMVar_hsa_circ_66108,RMVar_hsa_circ_173150,RMVar_hsa_circ_42800,RMVar_hsa_circ_26411,RMVar_hsa_circ_173161,RMVar_hsa_circ_173179,RMVar_hsa_circ_805,RMVar_hsa_circ_285487,RMVar_hsa_circ_173163,RMVar_hsa_circ_358449,RMVar_hsa_circ_362238,RMVar_hsa_circ_314344,RMVar_hsa_circ_173164,RMVar_hsa_circ_329550,RMVar_hsa_circ_54421,RMVar_hsa_circ_67906,RMVar_hsa_circ_282720,RMVar_hsa_circ_36448,RMVar_hsa_circ_173173,RMVar_hsa_circ_173171,RMVar_hsa_circ_339218,RMVar_hsa_circ_298216,RMVar_hsa_circ_126780,RMVar_hsa_circ_65288,RMVar_hsa_circ_173172,RMVar_hsa_circ_278237,RMVar_hsa_circ_59905,RMVar_hsa_circ_292792,RMVar_hsa_circ_173177,RMVar_hsa_circ_14268,RMVar_hsa_circ_321021,RMVar_hsa_circ_356719,RMVar_hsa_circ_348803,RMVar_hsa_circ_298421,RMVar_hsa_circ_110309,RMVar_hsa_circ_173180,RMVar_hsa_circ_173181,RMVar_hsa_circ_173183,RMVar_hsa_circ_173185,RMVar_hsa_circ_304187,RMVar_hsa_circ_336927,RMVar_hsa_circ_173178,RMVar_hsa_circ_329167,RMVar_hsa_circ_282183,RMVar_hsa_circ_173184,RMVar_hsa_circ_173182 39123 RMVar_ID_39123 Human_SNP_ID_581000252 A-to-I Human chr15 - 65493082 65493082 65493082 CAAAACTCCGTCTAAAAAAAAAGAGAGAAAGAAAGAAAACAGAAAAGGAAAGAAAAGAAAGAAAA CAAAACTCCGTCTAAAAAAAAAGAGAGAAAGAGAGAAAACAGAAAAGGAAAGAAAAGAAAGAAAA T C DPP8 Ensembl:ENSG00000074603 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs610683 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_173141,RMVar_hsa_circ_336881,RMVar_hsa_circ_112272,RMVar_hsa_circ_173139,RMVar_hsa_circ_173140,RMVar_hsa_circ_331946,RMVar_hsa_circ_279543,RMVar_hsa_circ_173142,RMVar_hsa_circ_45117,RMVar_hsa_circ_364428,RMVar_hsa_circ_102378,RMVar_hsa_circ_316014,RMVar_hsa_circ_173149,RMVar_hsa_circ_294122,RMVar_hsa_circ_282712,RMVar_hsa_circ_66108,RMVar_hsa_circ_173150,RMVar_hsa_circ_42800,RMVar_hsa_circ_26411,RMVar_hsa_circ_173161,RMVar_hsa_circ_173179,RMVar_hsa_circ_805,RMVar_hsa_circ_285487,RMVar_hsa_circ_173163,RMVar_hsa_circ_358449,RMVar_hsa_circ_362238,RMVar_hsa_circ_314344,RMVar_hsa_circ_173164,RMVar_hsa_circ_329550,RMVar_hsa_circ_54421,RMVar_hsa_circ_67906,RMVar_hsa_circ_282720,RMVar_hsa_circ_36448,RMVar_hsa_circ_173173,RMVar_hsa_circ_173171,RMVar_hsa_circ_339218,RMVar_hsa_circ_298216,RMVar_hsa_circ_126780,RMVar_hsa_circ_65288,RMVar_hsa_circ_173172,RMVar_hsa_circ_278237,RMVar_hsa_circ_59905,RMVar_hsa_circ_292792,RMVar_hsa_circ_173177,RMVar_hsa_circ_14268,RMVar_hsa_circ_321021,RMVar_hsa_circ_356719,RMVar_hsa_circ_348803,RMVar_hsa_circ_298421,RMVar_hsa_circ_110309,RMVar_hsa_circ_173180,RMVar_hsa_circ_173181,RMVar_hsa_circ_173183,RMVar_hsa_circ_173185,RMVar_hsa_circ_304187,RMVar_hsa_circ_336927,RMVar_hsa_circ_173178,RMVar_hsa_circ_329167,RMVar_hsa_circ_282183,RMVar_hsa_circ_173184,RMVar_hsa_circ_173182 39124 RMVar_ID_39124 Human_SNP_ID_581000870 A-to-I Human chr15 - 65495421 65495421 65495421 TTTTGTATTTTTAGTAGGGACGGGGTTTCACCATGTTGACCAGGCTGGTGTTGAACTCCTGACCT TTTTGTATTTTTAGTAGGGACGGGGTTTCACCCTGTTGACCAGGCTGGTGTTGAACTCCTGACCT T G DPP8 Ensembl:ENSG00000074603 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs933839003 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_173141,RMVar_hsa_circ_336881,RMVar_hsa_circ_112272,RMVar_hsa_circ_173139,RMVar_hsa_circ_173140,RMVar_hsa_circ_331946,RMVar_hsa_circ_279543,RMVar_hsa_circ_173142,RMVar_hsa_circ_45117,RMVar_hsa_circ_364428,RMVar_hsa_circ_102378,RMVar_hsa_circ_316014,RMVar_hsa_circ_173149,RMVar_hsa_circ_294122,RMVar_hsa_circ_282712,RMVar_hsa_circ_66108,RMVar_hsa_circ_173150,RMVar_hsa_circ_42800,RMVar_hsa_circ_26411,RMVar_hsa_circ_173161,RMVar_hsa_circ_173179,RMVar_hsa_circ_805,RMVar_hsa_circ_285487,RMVar_hsa_circ_173163,RMVar_hsa_circ_358449,RMVar_hsa_circ_362238,RMVar_hsa_circ_314344,RMVar_hsa_circ_173164,RMVar_hsa_circ_329550,RMVar_hsa_circ_54421,RMVar_hsa_circ_67906,RMVar_hsa_circ_282720,RMVar_hsa_circ_36448,RMVar_hsa_circ_173173,RMVar_hsa_circ_173171,RMVar_hsa_circ_339218,RMVar_hsa_circ_298216,RMVar_hsa_circ_126780,RMVar_hsa_circ_65288,RMVar_hsa_circ_173172,RMVar_hsa_circ_278237,RMVar_hsa_circ_59905,RMVar_hsa_circ_292792,RMVar_hsa_circ_173177,RMVar_hsa_circ_14268,RMVar_hsa_circ_321021,RMVar_hsa_circ_356719,RMVar_hsa_circ_348803,RMVar_hsa_circ_298421,RMVar_hsa_circ_110309,RMVar_hsa_circ_173180,RMVar_hsa_circ_173181,RMVar_hsa_circ_173183,RMVar_hsa_circ_173185,RMVar_hsa_circ_304187,RMVar_hsa_circ_336927,RMVar_hsa_circ_173178,RMVar_hsa_circ_329167,RMVar_hsa_circ_282183,RMVar_hsa_circ_173184,RMVar_hsa_circ_173182 39125 RMVar_ID_39125 Human_SNP_ID_581000911 A-to-I Human chr15 - 65495584 65495584 65495584 TTTGTTTGTTTTTTGTAACAAAGTCTCGCTCTATTGCCCAGGCTGGAGTGCAGTGGGCTATCTCA TTTGTTTGTTTTTTGTAACAAAGTCTCGCTCTGTTGCCCAGGCTGGAGTGCAGTGGGCTATCTCA T C DPP8 Ensembl:ENSG00000074603 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1178389502 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5178935 RMVar_hsa_circ_173141,RMVar_hsa_circ_336881,RMVar_hsa_circ_112272,RMVar_hsa_circ_173139,RMVar_hsa_circ_173140,RMVar_hsa_circ_331946,RMVar_hsa_circ_279543,RMVar_hsa_circ_173142,RMVar_hsa_circ_45117,RMVar_hsa_circ_364428,RMVar_hsa_circ_102378,RMVar_hsa_circ_316014,RMVar_hsa_circ_173149,RMVar_hsa_circ_294122,RMVar_hsa_circ_282712,RMVar_hsa_circ_66108,RMVar_hsa_circ_173150,RMVar_hsa_circ_42800,RMVar_hsa_circ_26411,RMVar_hsa_circ_173161,RMVar_hsa_circ_173179,RMVar_hsa_circ_805,RMVar_hsa_circ_285487,RMVar_hsa_circ_173163,RMVar_hsa_circ_358449,RMVar_hsa_circ_362238,RMVar_hsa_circ_314344,RMVar_hsa_circ_173164,RMVar_hsa_circ_329550,RMVar_hsa_circ_54421,RMVar_hsa_circ_67906,RMVar_hsa_circ_282720,RMVar_hsa_circ_36448,RMVar_hsa_circ_173173,RMVar_hsa_circ_173171,RMVar_hsa_circ_339218,RMVar_hsa_circ_298216,RMVar_hsa_circ_126780,RMVar_hsa_circ_65288,RMVar_hsa_circ_173172,RMVar_hsa_circ_278237,RMVar_hsa_circ_59905,RMVar_hsa_circ_292792,RMVar_hsa_circ_173177,RMVar_hsa_circ_14268,RMVar_hsa_circ_321021,RMVar_hsa_circ_356719,RMVar_hsa_circ_348803,RMVar_hsa_circ_298421,RMVar_hsa_circ_110309,RMVar_hsa_circ_173180,RMVar_hsa_circ_173181,RMVar_hsa_circ_173183,RMVar_hsa_circ_173185,RMVar_hsa_circ_304187,RMVar_hsa_circ_336927,RMVar_hsa_circ_173178,RMVar_hsa_circ_329167,RMVar_hsa_circ_282183,RMVar_hsa_circ_173184,RMVar_hsa_circ_173182 39126 RMVar_ID_39126 Human_SNP_ID_581000914 A-to-I Human chr15 - 65495596 65495596 65495596 GTGCTCAGCCTGTTTGTTTGTTTTTTGTAACAAAGTCTCGCTCTATTGCCCAGGCTGGAGTGCAG GTGCTCAGCCTGTTTGTTTGTTTTTTGTAACAGAGTCTCGCTCTATTGCCCAGGCTGGAGTGCAG T C DPP8 Ensembl:ENSG00000074603 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs893794389 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_173141,RMVar_hsa_circ_336881,RMVar_hsa_circ_112272,RMVar_hsa_circ_173139,RMVar_hsa_circ_173140,RMVar_hsa_circ_331946,RMVar_hsa_circ_279543,RMVar_hsa_circ_173142,RMVar_hsa_circ_45117,RMVar_hsa_circ_364428,RMVar_hsa_circ_102378,RMVar_hsa_circ_316014,RMVar_hsa_circ_173149,RMVar_hsa_circ_294122,RMVar_hsa_circ_282712,RMVar_hsa_circ_66108,RMVar_hsa_circ_173150,RMVar_hsa_circ_42800,RMVar_hsa_circ_26411,RMVar_hsa_circ_173161,RMVar_hsa_circ_173179,RMVar_hsa_circ_805,RMVar_hsa_circ_285487,RMVar_hsa_circ_173163,RMVar_hsa_circ_358449,RMVar_hsa_circ_362238,RMVar_hsa_circ_314344,RMVar_hsa_circ_173164,RMVar_hsa_circ_329550,RMVar_hsa_circ_54421,RMVar_hsa_circ_67906,RMVar_hsa_circ_282720,RMVar_hsa_circ_36448,RMVar_hsa_circ_173173,RMVar_hsa_circ_173171,RMVar_hsa_circ_339218,RMVar_hsa_circ_298216,RMVar_hsa_circ_126780,RMVar_hsa_circ_65288,RMVar_hsa_circ_173172,RMVar_hsa_circ_278237,RMVar_hsa_circ_59905,RMVar_hsa_circ_292792,RMVar_hsa_circ_173177,RMVar_hsa_circ_14268,RMVar_hsa_circ_321021,RMVar_hsa_circ_356719,RMVar_hsa_circ_348803,RMVar_hsa_circ_298421,RMVar_hsa_circ_110309,RMVar_hsa_circ_173180,RMVar_hsa_circ_173181,RMVar_hsa_circ_173183,RMVar_hsa_circ_173185,RMVar_hsa_circ_304187,RMVar_hsa_circ_336927,RMVar_hsa_circ_173178,RMVar_hsa_circ_329167,RMVar_hsa_circ_282183,RMVar_hsa_circ_173184,RMVar_hsa_circ_173182 39127 RMVar_ID_39127 Human_SNP_ID_581000963 A-to-I Human chr15 - 65495736 65495736 65495736 CTGGGATTACCGGCTAATTTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGG CTGGGATTACCGGCTAATTTTTTTGTATTTTTGGTAGAGACGGGGTTTCACCATGTTGGCCAGGG T C DPP8 Ensembl:ENSG00000074603 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs946720972 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_173141,RMVar_hsa_circ_336881,RMVar_hsa_circ_112272,RMVar_hsa_circ_173139,RMVar_hsa_circ_173140,RMVar_hsa_circ_331946,RMVar_hsa_circ_279543,RMVar_hsa_circ_173142,RMVar_hsa_circ_45117,RMVar_hsa_circ_364428,RMVar_hsa_circ_102378,RMVar_hsa_circ_316014,RMVar_hsa_circ_173149,RMVar_hsa_circ_294122,RMVar_hsa_circ_282712,RMVar_hsa_circ_66108,RMVar_hsa_circ_173150,RMVar_hsa_circ_42800,RMVar_hsa_circ_26411,RMVar_hsa_circ_173161,RMVar_hsa_circ_173179,RMVar_hsa_circ_805,RMVar_hsa_circ_285487,RMVar_hsa_circ_173163,RMVar_hsa_circ_358449,RMVar_hsa_circ_362238,RMVar_hsa_circ_314344,RMVar_hsa_circ_173164,RMVar_hsa_circ_329550,RMVar_hsa_circ_54421,RMVar_hsa_circ_67906,RMVar_hsa_circ_282720,RMVar_hsa_circ_36448,RMVar_hsa_circ_173173,RMVar_hsa_circ_173171,RMVar_hsa_circ_339218,RMVar_hsa_circ_298216,RMVar_hsa_circ_126780,RMVar_hsa_circ_65288,RMVar_hsa_circ_173172,RMVar_hsa_circ_278237,RMVar_hsa_circ_59905,RMVar_hsa_circ_292792,RMVar_hsa_circ_173177,RMVar_hsa_circ_14268,RMVar_hsa_circ_321021,RMVar_hsa_circ_356719,RMVar_hsa_circ_348803,RMVar_hsa_circ_298421,RMVar_hsa_circ_110309,RMVar_hsa_circ_173180,RMVar_hsa_circ_173181,RMVar_hsa_circ_173183,RMVar_hsa_circ_173185,RMVar_hsa_circ_304187,RMVar_hsa_circ_336927,RMVar_hsa_circ_173178,RMVar_hsa_circ_329167,RMVar_hsa_circ_282183,RMVar_hsa_circ_173184,RMVar_hsa_circ_173182 39128 RMVar_ID_39128 Human_SNP_ID_581001006 A-to-I Human chr15 - 65495876 65495875 65495877 TGTTCTTTTTTGTTGTTGTTTGTTTTTGAGACAGAGTCTTACTGTGTCACCCAGGCTGGAGTGCA TGTTCTTTTTTGTTGTTGTTTGTTTTTGAGA__GAGTCTTACTGTGTCACCCAGGCTGGAGTGCA CTG C DPP8 Ensembl:ENSG00000074603 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1383063142 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_173141,RMVar_hsa_circ_336881,RMVar_hsa_circ_112272,RMVar_hsa_circ_173139,RMVar_hsa_circ_173140,RMVar_hsa_circ_331946,RMVar_hsa_circ_279543,RMVar_hsa_circ_173142,RMVar_hsa_circ_45117,RMVar_hsa_circ_364428,RMVar_hsa_circ_102378,RMVar_hsa_circ_316014,RMVar_hsa_circ_173149,RMVar_hsa_circ_294122,RMVar_hsa_circ_282712,RMVar_hsa_circ_66108,RMVar_hsa_circ_173150,RMVar_hsa_circ_42800,RMVar_hsa_circ_26411,RMVar_hsa_circ_173161,RMVar_hsa_circ_173179,RMVar_hsa_circ_805,RMVar_hsa_circ_285487,RMVar_hsa_circ_173163,RMVar_hsa_circ_358449,RMVar_hsa_circ_362238,RMVar_hsa_circ_314344,RMVar_hsa_circ_173164,RMVar_hsa_circ_329550,RMVar_hsa_circ_54421,RMVar_hsa_circ_67906,RMVar_hsa_circ_282720,RMVar_hsa_circ_36448,RMVar_hsa_circ_173173,RMVar_hsa_circ_173171,RMVar_hsa_circ_339218,RMVar_hsa_circ_298216,RMVar_hsa_circ_126780,RMVar_hsa_circ_65288,RMVar_hsa_circ_173172,RMVar_hsa_circ_278237,RMVar_hsa_circ_59905,RMVar_hsa_circ_292792,RMVar_hsa_circ_173177,RMVar_hsa_circ_14268,RMVar_hsa_circ_321021,RMVar_hsa_circ_356719,RMVar_hsa_circ_348803,RMVar_hsa_circ_298421,RMVar_hsa_circ_110309,RMVar_hsa_circ_173180,RMVar_hsa_circ_173181,RMVar_hsa_circ_173183,RMVar_hsa_circ_173185,RMVar_hsa_circ_304187,RMVar_hsa_circ_336927,RMVar_hsa_circ_173178,RMVar_hsa_circ_329167,RMVar_hsa_circ_282183,RMVar_hsa_circ_173184,RMVar_hsa_circ_173182 39129 RMVar_ID_39129 Human_SNP_ID_581001089 A-to-I Human chr15 - 65496122 65496122 65496122 AAAATTAGCCGGGCGTGGTGGCGGGTGCCTGTAGTCCCAGCTACTAAGGAGGCCAAGGCAGGAGA AAAATTAGCCGGGCGTGGTGGCGGGTGCCTGTGGTCCCAGCTACTAAGGAGGCCAAGGCAGGAGA T C DPP8 Ensembl:ENSG00000074603 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs892559553 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_173141,RMVar_hsa_circ_336881,RMVar_hsa_circ_112272,RMVar_hsa_circ_173139,RMVar_hsa_circ_173140,RMVar_hsa_circ_331946,RMVar_hsa_circ_279543,RMVar_hsa_circ_173142,RMVar_hsa_circ_45117,RMVar_hsa_circ_364428,RMVar_hsa_circ_102378,RMVar_hsa_circ_316014,RMVar_hsa_circ_173149,RMVar_hsa_circ_294122,RMVar_hsa_circ_282712,RMVar_hsa_circ_66108,RMVar_hsa_circ_173150,RMVar_hsa_circ_42800,RMVar_hsa_circ_26411,RMVar_hsa_circ_173161,RMVar_hsa_circ_173179,RMVar_hsa_circ_805,RMVar_hsa_circ_285487,RMVar_hsa_circ_173163,RMVar_hsa_circ_358449,RMVar_hsa_circ_362238,RMVar_hsa_circ_314344,RMVar_hsa_circ_173164,RMVar_hsa_circ_329550,RMVar_hsa_circ_54421,RMVar_hsa_circ_67906,RMVar_hsa_circ_282720,RMVar_hsa_circ_36448,RMVar_hsa_circ_173173,RMVar_hsa_circ_173171,RMVar_hsa_circ_339218,RMVar_hsa_circ_298216,RMVar_hsa_circ_126780,RMVar_hsa_circ_65288,RMVar_hsa_circ_173172,RMVar_hsa_circ_278237,RMVar_hsa_circ_59905,RMVar_hsa_circ_292792,RMVar_hsa_circ_173177,RMVar_hsa_circ_14268,RMVar_hsa_circ_321021,RMVar_hsa_circ_356719,RMVar_hsa_circ_348803,RMVar_hsa_circ_298421,RMVar_hsa_circ_110309,RMVar_hsa_circ_173180,RMVar_hsa_circ_173181,RMVar_hsa_circ_173183,RMVar_hsa_circ_173185,RMVar_hsa_circ_304187,RMVar_hsa_circ_336927,RMVar_hsa_circ_173178,RMVar_hsa_circ_329167,RMVar_hsa_circ_282183,RMVar_hsa_circ_173184,RMVar_hsa_circ_173182 39130 RMVar_ID_39130 Human_SNP_ID_581001426 A-to-I Human chr15 - 65497388 65497388 65497388 ATTAGCTGAGCGTAGTGGCATGTGTAGTCCCAACTACCTGGGAGATTGAGGTAGGAGGATCACCT ATTAGCTGAGCGTAGTGGCATGTGTAGTCCCAGCTACCTGGGAGATTGAGGTAGGAGGATCACCT T C DPP8 Ensembl:ENSG00000074603 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs410380 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_114,Clinvar_Rec_115 GWAS_ID_4462,GWAS_ID_4463,GWAS_ID_4464,GWAS_ID_4465,GWAS_ID_4466,GWAS_ID_4467,GWAS_ID_4468,GWAS_ID_4469,GWAS_ID_4470,GWAS_ID_4471,GWAS_ID_4472,GWAS_ID_4473,GWAS_ID_4474,GWAS_ID_4475,GWAS_ID_4476,GWAS_ID_4477,GWAS_ID_4478,GWAS_ID_4479,GWAS_ID_4480,GWAS_ID_4481,GWAS_ID_4482,GWAS_ID_4483,GWAS_ID_4484,GWAS_ID_4485,GWAS_ID_4486,GWAS_ID_4487,GWAS_ID_4488,GWAS_ID_4489,GWAS_ID_4490,GWAS_ID_4491,GWAS_ID_4492,GWAS_ID_4493,GWAS_ID_4494,GWAS_ID_4495,GWAS_ID_4496,GWAS_ID_4497,GWAS_ID_4498,GWAS_ID_4499,GWAS_ID_4500,GWAS_ID_4501,GWAS_ID_4502,GWAS_ID_4503,GWAS_ID_4504,GWAS_ID_4505,GWAS_ID_4506,GWAS_ID_4507,GWAS_ID_4508,GWAS_ID_4509,GWAS_ID_4510,GWAS_ID_4511,GWAS_ID_4512,GWAS_ID_4513,GWAS_ID_4514,GWAS_ID_4515,GWAS_ID_4516,GWAS_ID_4517,GWAS_ID_4518,GWAS_ID_4519,GWAS_ID_4520,GWAS_ID_4521,GWAS_ID_4522,GWAS_ID_4523,GWAS_ID_4524,GWAS_ID_4525,GWAS_ID_4526,GWAS_ID_4527,GWAS_ID_4528,GWAS_ID_4529,GWAS_ID_4530,GWAS_ID_4531,GWAS_ID_4532,GWAS_ID_4533,GWAS_ID_4534,GWAS_ID_4535,GWAS_ID_4536,GWAS_ID_4537,GWAS_ID_4538,GWAS_ID_4539,GWAS_ID_4540,GWAS_ID_4541,GWAS_ID_4542,GWAS_ID_4543,GWAS_ID_4544,GWAS_ID_4545,GWAS_ID_4546,GWAS_ID_4547,GWAS_ID_4548,GWAS_ID_4549,GWAS_ID_4550,GWAS_ID_4551,GWAS_ID_4552,GWAS_ID_4553,GWAS_ID_4554,GWAS_ID_4555,GWAS_ID_4556,GWAS_ID_4557,GWAS_ID_4558,GWAS_ID_4559,GWAS_ID_4560,GWAS_ID_4561,GWAS_ID_4562,GWAS_ID_4563,GWAS_ID_4564,GWAS_ID_4565,GWAS_ID_4566,GWAS_ID_4567,GWAS_ID_4568,GWAS_ID_4569,GWAS_ID_4570,GWAS_ID_4571,GWAS_ID_4572,GWAS_ID_4573,GWAS_ID_4574,GWAS_ID_4575,GWAS_ID_4576,GWAS_ID_4577,GWAS_ID_4578,GWAS_ID_4579,GWAS_ID_4580,GWAS_ID_4581,GWAS_ID_4582,GWAS_ID_4583,GWAS_ID_4584,GWAS_ID_4585,GWAS_ID_4586,GWAS_ID_4587,GWAS_ID_4588,GWAS_ID_4589,GWAS_ID_4590,GWAS_ID_4591,GWAS_ID_4592 RMVar_hsa_circ_173141,RMVar_hsa_circ_336881,RMVar_hsa_circ_112272,RMVar_hsa_circ_173139,RMVar_hsa_circ_173140,RMVar_hsa_circ_331946,RMVar_hsa_circ_279543,RMVar_hsa_circ_173142,RMVar_hsa_circ_45117,RMVar_hsa_circ_364428,RMVar_hsa_circ_102378,RMVar_hsa_circ_316014,RMVar_hsa_circ_173149,RMVar_hsa_circ_294122,RMVar_hsa_circ_282712,RMVar_hsa_circ_66108,RMVar_hsa_circ_173150,RMVar_hsa_circ_42800,RMVar_hsa_circ_26411,RMVar_hsa_circ_173161,RMVar_hsa_circ_173179,RMVar_hsa_circ_805,RMVar_hsa_circ_285487,RMVar_hsa_circ_173163,RMVar_hsa_circ_358449,RMVar_hsa_circ_362238,RMVar_hsa_circ_314344,RMVar_hsa_circ_173164,RMVar_hsa_circ_329550,RMVar_hsa_circ_54421,RMVar_hsa_circ_67906,RMVar_hsa_circ_282720,RMVar_hsa_circ_36448,RMVar_hsa_circ_173173,RMVar_hsa_circ_173171,RMVar_hsa_circ_339218,RMVar_hsa_circ_298216,RMVar_hsa_circ_126780,RMVar_hsa_circ_65288,RMVar_hsa_circ_173172,RMVar_hsa_circ_278237,RMVar_hsa_circ_59905,RMVar_hsa_circ_292792,RMVar_hsa_circ_173177,RMVar_hsa_circ_14268,RMVar_hsa_circ_321021,RMVar_hsa_circ_356719,RMVar_hsa_circ_348803,RMVar_hsa_circ_298421,RMVar_hsa_circ_110309,RMVar_hsa_circ_173180,RMVar_hsa_circ_173181,RMVar_hsa_circ_173183,RMVar_hsa_circ_173185,RMVar_hsa_circ_304187,RMVar_hsa_circ_336927,RMVar_hsa_circ_173178,RMVar_hsa_circ_329167,RMVar_hsa_circ_282183,RMVar_hsa_circ_173184,RMVar_hsa_circ_173182 39131 RMVar_ID_39131 Human_SNP_ID_581001662 A-to-I Human chr15 - 65498265 65498265 65498265 GGTGCCCACCACTATGCCCAGCTAATTTTTGTATTTTTGGTAGAGATGGGGTTTCACTATGTTGG GGTGCCCACCACTATGCCCAGCTAATTTTTGTGTTTTTGGTAGAGATGGGGTTTCACTATGTTGG T C DPP8 Ensembl:ENSG00000074603 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs976273533 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_173141,RMVar_hsa_circ_336881,RMVar_hsa_circ_173140,RMVar_hsa_circ_331946,RMVar_hsa_circ_279543,RMVar_hsa_circ_173142,RMVar_hsa_circ_45117,RMVar_hsa_circ_364428,RMVar_hsa_circ_316014,RMVar_hsa_circ_294122,RMVar_hsa_circ_282712,RMVar_hsa_circ_66108,RMVar_hsa_circ_173150,RMVar_hsa_circ_42800,RMVar_hsa_circ_26411,RMVar_hsa_circ_173161,RMVar_hsa_circ_173179,RMVar_hsa_circ_805,RMVar_hsa_circ_285487,RMVar_hsa_circ_173163,RMVar_hsa_circ_358449,RMVar_hsa_circ_362238,RMVar_hsa_circ_314344,RMVar_hsa_circ_173164,RMVar_hsa_circ_329550,RMVar_hsa_circ_54421,RMVar_hsa_circ_67906,RMVar_hsa_circ_282720,RMVar_hsa_circ_173173,RMVar_hsa_circ_173171,RMVar_hsa_circ_339218,RMVar_hsa_circ_298216,RMVar_hsa_circ_126780,RMVar_hsa_circ_65288,RMVar_hsa_circ_173172,RMVar_hsa_circ_278237,RMVar_hsa_circ_59905,RMVar_hsa_circ_292792,RMVar_hsa_circ_173177,RMVar_hsa_circ_356719,RMVar_hsa_circ_348803,RMVar_hsa_circ_298421,RMVar_hsa_circ_110309,RMVar_hsa_circ_173180,RMVar_hsa_circ_173181,RMVar_hsa_circ_119735,RMVar_hsa_circ_173183,RMVar_hsa_circ_304187,RMVar_hsa_circ_329167,RMVar_hsa_circ_282183,RMVar_hsa_circ_173184,RMVar_hsa_circ_284324,RMVar_hsa_circ_290297,RMVar_hsa_circ_173182,RMVar_hsa_circ_324699,RMVar_hsa_circ_275167,RMVar_hsa_circ_173189,RMVar_hsa_circ_173191,RMVar_hsa_circ_77240,RMVar_hsa_circ_173192,RMVar_hsa_circ_173190,RMVar_hsa_circ_173187,RMVar_hsa_circ_173188 39132 RMVar_ID_39132 Human_SNP_ID_581002327 A-to-I Human chr15 - 65500310 65500310 65500310 GGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCATGCGCCACCACC GGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCATGCGCCACCACC T C DPP8 Ensembl:ENSG00000074603 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1332124551 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_173141,RMVar_hsa_circ_336881,RMVar_hsa_circ_173140,RMVar_hsa_circ_331946,RMVar_hsa_circ_279543,RMVar_hsa_circ_173142,RMVar_hsa_circ_45117,RMVar_hsa_circ_364428,RMVar_hsa_circ_316014,RMVar_hsa_circ_294122,RMVar_hsa_circ_282712,RMVar_hsa_circ_66108,RMVar_hsa_circ_173150,RMVar_hsa_circ_42800,RMVar_hsa_circ_26411,RMVar_hsa_circ_173161,RMVar_hsa_circ_173179,RMVar_hsa_circ_805,RMVar_hsa_circ_285487,RMVar_hsa_circ_173163,RMVar_hsa_circ_358449,RMVar_hsa_circ_362238,RMVar_hsa_circ_314344,RMVar_hsa_circ_173164,RMVar_hsa_circ_329550,RMVar_hsa_circ_54421,RMVar_hsa_circ_67906,RMVar_hsa_circ_282720,RMVar_hsa_circ_173173,RMVar_hsa_circ_173171,RMVar_hsa_circ_339218,RMVar_hsa_circ_298216,RMVar_hsa_circ_126780,RMVar_hsa_circ_65288,RMVar_hsa_circ_173172,RMVar_hsa_circ_278237,RMVar_hsa_circ_59905,RMVar_hsa_circ_292792,RMVar_hsa_circ_173177,RMVar_hsa_circ_356719,RMVar_hsa_circ_348803,RMVar_hsa_circ_298421,RMVar_hsa_circ_110309,RMVar_hsa_circ_173180,RMVar_hsa_circ_173181,RMVar_hsa_circ_119735,RMVar_hsa_circ_173183,RMVar_hsa_circ_304187,RMVar_hsa_circ_329167,RMVar_hsa_circ_282183,RMVar_hsa_circ_173184,RMVar_hsa_circ_284324,RMVar_hsa_circ_290297,RMVar_hsa_circ_173182,RMVar_hsa_circ_324699,RMVar_hsa_circ_275167,RMVar_hsa_circ_173189,RMVar_hsa_circ_173191,RMVar_hsa_circ_77240,RMVar_hsa_circ_173192,RMVar_hsa_circ_173190,RMVar_hsa_circ_173187,RMVar_hsa_circ_173188 39133 RMVar_ID_39133 Human_SNP_ID_581002554 A-to-I Human chr15 - 65501010 65501010 65501010 AGCTGGGCGTGGTTGCGGGCGCCTGTAGTCCCAGCTACTAGGAAGGCTGAGGCAGGAGAATGGTG AGCTGGGCGTGGTTGCGGGCGCCTGTAGTCCCGGCTACTAGGAAGGCTGAGGCAGGAGAATGGTG T C DPP8 Ensembl:ENSG00000074603 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1000781384 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_122651 RMVar_hsa_circ_173141,RMVar_hsa_circ_336881,RMVar_hsa_circ_173140,RMVar_hsa_circ_331946,RMVar_hsa_circ_279543,RMVar_hsa_circ_173142,RMVar_hsa_circ_45117,RMVar_hsa_circ_364428,RMVar_hsa_circ_316014,RMVar_hsa_circ_282712,RMVar_hsa_circ_66108,RMVar_hsa_circ_173150,RMVar_hsa_circ_42800,RMVar_hsa_circ_26411,RMVar_hsa_circ_173161,RMVar_hsa_circ_805,RMVar_hsa_circ_285487,RMVar_hsa_circ_173163,RMVar_hsa_circ_358449,RMVar_hsa_circ_314344,RMVar_hsa_circ_173164,RMVar_hsa_circ_329550,RMVar_hsa_circ_54421,RMVar_hsa_circ_282720,RMVar_hsa_circ_173173,RMVar_hsa_circ_173171,RMVar_hsa_circ_298216,RMVar_hsa_circ_126780,RMVar_hsa_circ_173172,RMVar_hsa_circ_278237,RMVar_hsa_circ_59905,RMVar_hsa_circ_292792,RMVar_hsa_circ_173177,RMVar_hsa_circ_356719,RMVar_hsa_circ_298421,RMVar_hsa_circ_110309,RMVar_hsa_circ_173180,RMVar_hsa_circ_173181,RMVar_hsa_circ_2274,RMVar_hsa_circ_119735,RMVar_hsa_circ_173183,RMVar_hsa_circ_329167,RMVar_hsa_circ_282183,RMVar_hsa_circ_284324,RMVar_hsa_circ_173182,RMVar_hsa_circ_324699,RMVar_hsa_circ_275167,RMVar_hsa_circ_173189,RMVar_hsa_circ_173191,RMVar_hsa_circ_77240,RMVar_hsa_circ_173192,RMVar_hsa_circ_173190,RMVar_hsa_circ_173188,RMVar_hsa_circ_283525,RMVar_hsa_circ_173193 39134 RMVar_ID_39134 Human_SNP_ID_581003305 A-to-I Human chr15 - 65503897 65503897 65503897 GAAAAGGCCAGGTGCGGTCGCTTATGCCTGTAATCTCAGCACTTTGGGAGGCTGAGGCGGGTGGA GAAAAGGCCAGGTGCGGTCGCTTATGCCTGTAGTCTCAGCACTTTGGGAGGCTGAGGCGGGTGGA T C DPP8 Ensembl:ENSG00000074603 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1372464792 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_173141,RMVar_hsa_circ_336881,RMVar_hsa_circ_173140,RMVar_hsa_circ_331946,RMVar_hsa_circ_279543,RMVar_hsa_circ_173142,RMVar_hsa_circ_45117,RMVar_hsa_circ_364428,RMVar_hsa_circ_316014,RMVar_hsa_circ_282712,RMVar_hsa_circ_66108,RMVar_hsa_circ_173150,RMVar_hsa_circ_42800,RMVar_hsa_circ_26411,RMVar_hsa_circ_173161,RMVar_hsa_circ_805,RMVar_hsa_circ_285487,RMVar_hsa_circ_173163,RMVar_hsa_circ_358449,RMVar_hsa_circ_314344,RMVar_hsa_circ_173164,RMVar_hsa_circ_329550,RMVar_hsa_circ_54421,RMVar_hsa_circ_282720,RMVar_hsa_circ_173173,RMVar_hsa_circ_173171,RMVar_hsa_circ_298216,RMVar_hsa_circ_126780,RMVar_hsa_circ_173172,RMVar_hsa_circ_278237,RMVar_hsa_circ_59905,RMVar_hsa_circ_292792,RMVar_hsa_circ_173177,RMVar_hsa_circ_356719,RMVar_hsa_circ_298421,RMVar_hsa_circ_110309,RMVar_hsa_circ_173180,RMVar_hsa_circ_173181,RMVar_hsa_circ_2274,RMVar_hsa_circ_119735,RMVar_hsa_circ_173183,RMVar_hsa_circ_329167,RMVar_hsa_circ_282183,RMVar_hsa_circ_284324,RMVar_hsa_circ_173182,RMVar_hsa_circ_324699,RMVar_hsa_circ_275167,RMVar_hsa_circ_173189,RMVar_hsa_circ_173191,RMVar_hsa_circ_77240,RMVar_hsa_circ_173192,RMVar_hsa_circ_173190,RMVar_hsa_circ_173188,RMVar_hsa_circ_283525,RMVar_hsa_circ_173193 39135 RMVar_ID_39135 Human_SNP_ID_581003882 A-to-I Human chr15 - 65505793 65505793 65505793 GGTGCACACCACCATGCCTGGCTAATTTTTGTATTTTCAGTAGAGACGGGGTTTCATCATGTCAC GGTGCACACCACCATGCCTGGCTAATTTTTGTGTTTTCAGTAGAGACGGGGTTTCATCATGTCAC T C DPP8 Ensembl:ENSG00000074603 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs918797425 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12556883 RMVar_hsa_circ_173141,RMVar_hsa_circ_336881,RMVar_hsa_circ_173140,RMVar_hsa_circ_331946,RMVar_hsa_circ_279543,RMVar_hsa_circ_173142,RMVar_hsa_circ_45117,RMVar_hsa_circ_364428,RMVar_hsa_circ_316014,RMVar_hsa_circ_282712,RMVar_hsa_circ_66108,RMVar_hsa_circ_173150,RMVar_hsa_circ_42800,RMVar_hsa_circ_26411,RMVar_hsa_circ_173161,RMVar_hsa_circ_805,RMVar_hsa_circ_285487,RMVar_hsa_circ_173163,RMVar_hsa_circ_358449,RMVar_hsa_circ_314344,RMVar_hsa_circ_173164,RMVar_hsa_circ_329550,RMVar_hsa_circ_54421,RMVar_hsa_circ_282720,RMVar_hsa_circ_173173,RMVar_hsa_circ_173171,RMVar_hsa_circ_298216,RMVar_hsa_circ_126780,RMVar_hsa_circ_173172,RMVar_hsa_circ_278237,RMVar_hsa_circ_59905,RMVar_hsa_circ_292792,RMVar_hsa_circ_173177,RMVar_hsa_circ_356719,RMVar_hsa_circ_298421,RMVar_hsa_circ_110309,RMVar_hsa_circ_173180,RMVar_hsa_circ_173181,RMVar_hsa_circ_2274,RMVar_hsa_circ_119735,RMVar_hsa_circ_173183,RMVar_hsa_circ_329167,RMVar_hsa_circ_282183,RMVar_hsa_circ_284324,RMVar_hsa_circ_173182,RMVar_hsa_circ_324699,RMVar_hsa_circ_275167,RMVar_hsa_circ_173189,RMVar_hsa_circ_173191,RMVar_hsa_circ_77240,RMVar_hsa_circ_173192,RMVar_hsa_circ_173190,RMVar_hsa_circ_173188,RMVar_hsa_circ_283525,RMVar_hsa_circ_173193 39136 RMVar_ID_39136 Human_SNP_ID_581003901 A-to-I Human chr15 - 65505903 65505903 65505903 CTCTGCAACCCAGGCTGGAGCGCAGTGGCGCAATCTTGGCTCACTGTAACTTCTGCCTCCCAGAT CTCTGCAACCCAGGCTGGAGCGCAGTGGCGCAGTCTTGGCTCACTGTAACTTCTGCCTCCCAGAT T C DPP8 Ensembl:ENSG00000074603 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs528469312 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12556884 RMVar_hsa_circ_173141,RMVar_hsa_circ_336881,RMVar_hsa_circ_173140,RMVar_hsa_circ_331946,RMVar_hsa_circ_279543,RMVar_hsa_circ_173142,RMVar_hsa_circ_45117,RMVar_hsa_circ_364428,RMVar_hsa_circ_316014,RMVar_hsa_circ_282712,RMVar_hsa_circ_66108,RMVar_hsa_circ_173150,RMVar_hsa_circ_42800,RMVar_hsa_circ_26411,RMVar_hsa_circ_173161,RMVar_hsa_circ_805,RMVar_hsa_circ_285487,RMVar_hsa_circ_173163,RMVar_hsa_circ_358449,RMVar_hsa_circ_314344,RMVar_hsa_circ_173164,RMVar_hsa_circ_329550,RMVar_hsa_circ_54421,RMVar_hsa_circ_282720,RMVar_hsa_circ_173173,RMVar_hsa_circ_173171,RMVar_hsa_circ_298216,RMVar_hsa_circ_126780,RMVar_hsa_circ_173172,RMVar_hsa_circ_278237,RMVar_hsa_circ_59905,RMVar_hsa_circ_292792,RMVar_hsa_circ_173177,RMVar_hsa_circ_356719,RMVar_hsa_circ_298421,RMVar_hsa_circ_110309,RMVar_hsa_circ_173180,RMVar_hsa_circ_173181,RMVar_hsa_circ_2274,RMVar_hsa_circ_119735,RMVar_hsa_circ_173183,RMVar_hsa_circ_329167,RMVar_hsa_circ_282183,RMVar_hsa_circ_284324,RMVar_hsa_circ_173182,RMVar_hsa_circ_324699,RMVar_hsa_circ_275167,RMVar_hsa_circ_173189,RMVar_hsa_circ_173191,RMVar_hsa_circ_77240,RMVar_hsa_circ_173192,RMVar_hsa_circ_173190,RMVar_hsa_circ_173188,RMVar_hsa_circ_283525,RMVar_hsa_circ_173193 39137 RMVar_ID_39137 Human_SNP_ID_581004008 A-to-I Human chr15 - 65506246 65506246 65506246 TGGCTCACTACAACCTCCGCCTCCCGGGTTCAAGCGATTCTCCTACCTCAGACTCCCAAGTAGCT TGGCTCACTACAACCTCCGCCTCCCGGGTTCACGCGATTCTCCTACCTCAGACTCCCAAGTAGCT T G DPP8 Ensembl:ENSG00000074603 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs150649020 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_173141,RMVar_hsa_circ_336881,RMVar_hsa_circ_173140,RMVar_hsa_circ_331946,RMVar_hsa_circ_279543,RMVar_hsa_circ_173142,RMVar_hsa_circ_45117,RMVar_hsa_circ_364428,RMVar_hsa_circ_316014,RMVar_hsa_circ_282712,RMVar_hsa_circ_66108,RMVar_hsa_circ_173150,RMVar_hsa_circ_42800,RMVar_hsa_circ_26411,RMVar_hsa_circ_173161,RMVar_hsa_circ_805,RMVar_hsa_circ_285487,RMVar_hsa_circ_173163,RMVar_hsa_circ_358449,RMVar_hsa_circ_314344,RMVar_hsa_circ_173164,RMVar_hsa_circ_329550,RMVar_hsa_circ_54421,RMVar_hsa_circ_282720,RMVar_hsa_circ_173173,RMVar_hsa_circ_173171,RMVar_hsa_circ_298216,RMVar_hsa_circ_126780,RMVar_hsa_circ_173172,RMVar_hsa_circ_278237,RMVar_hsa_circ_59905,RMVar_hsa_circ_292792,RMVar_hsa_circ_173177,RMVar_hsa_circ_356719,RMVar_hsa_circ_298421,RMVar_hsa_circ_110309,RMVar_hsa_circ_173180,RMVar_hsa_circ_173181,RMVar_hsa_circ_2274,RMVar_hsa_circ_119735,RMVar_hsa_circ_173183,RMVar_hsa_circ_329167,RMVar_hsa_circ_282183,RMVar_hsa_circ_284324,RMVar_hsa_circ_173182,RMVar_hsa_circ_324699,RMVar_hsa_circ_275167,RMVar_hsa_circ_173189,RMVar_hsa_circ_173191,RMVar_hsa_circ_77240,RMVar_hsa_circ_173192,RMVar_hsa_circ_173190,RMVar_hsa_circ_173188,RMVar_hsa_circ_283525,RMVar_hsa_circ_173193 39138 RMVar_ID_39138 Human_SNP_ID_581028894 A-to-I Human chr15 - 65604247 65604247 65604247 AAACCCCCATCTCTACTAAAAATACAAAAATTAGCTGGGTGTGGTGGTGTGCACCTGTAGTCCCA AAACCCCCATCTCTACTAAAAATACAAAAATTGGCTGGGTGTGGTGGTGTGCACCTGTAGTCCCA T C INTS14 Ensembl:ENSG00000138614 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs979527982 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_46165,RMVar_hsa_circ_69134,RMVar_hsa_circ_38939,RMVar_hsa_circ_341631,RMVar_hsa_circ_352881,RMVar_hsa_circ_353217,RMVar_hsa_circ_54809,RMVar_hsa_circ_300216,RMVar_hsa_circ_21310 39139 RMVar_ID_39139 Human_SNP_ID_581028900 A-to-I Human chr15 - 65604265 65604265 65604265 ATCCTGGCCAACATGGTGAAACCCCCATCTCTACTAAAAATACAAAAATTAGCTGGGTGTGGTGG ATCCTGGCCAACATGGTGAAACCCCCATCTCTGCTAAAAATACAAAAATTAGCTGGGTGTGGTGG T C INTS14 Ensembl:ENSG00000138614 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1026434256 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_46165,RMVar_hsa_circ_69134,RMVar_hsa_circ_38939,RMVar_hsa_circ_341631,RMVar_hsa_circ_352881,RMVar_hsa_circ_353217,RMVar_hsa_circ_54809,RMVar_hsa_circ_300216,RMVar_hsa_circ_21310 39140 RMVar_ID_39140 Human_SNP_ID_581029468 A-to-I Human chr15 - 65606505 65606505 65606505 CACGCCTGTAATCCCAGCACTTTGGGAAGCCAAGGCGAGAGGATCACTTGAGCCCAGGAGTTTGA CACGCCTGTAATCCCAGCACTTTGGGAAGCCAGGGCGAGAGGATCACTTGAGCCCAGGAGTTTGA T C INTS14 Ensembl:ENSG00000138614 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1477890561 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69134,RMVar_hsa_circ_38939,RMVar_hsa_circ_350271,RMVar_hsa_circ_21310,RMVar_hsa_circ_327667 39141 RMVar_ID_39141 Human_SNP_ID_581043586 A-to-I Human chr15 - 65668391 65668391 65668391 CAGCCTGGACAACATGGCAAAACCCCATCTCTACTAAAAATACAAAAATTAGGCAGGCATGGTGG CAGCCTGGACAACATGGCAAAACCCCATCTCTGCTAAAAATACAAAAATTAGGCAGGCATGGTGG T C DENND4A Ensembl:ENSG00000174485 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs937476171 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6097,RMVar_hsa_circ_173209,RMVar_hsa_circ_107085,RMVar_hsa_circ_32518,RMVar_hsa_circ_12376,RMVar_hsa_circ_173215,RMVar_hsa_circ_12416,RMVar_hsa_circ_66248,RMVar_hsa_circ_90364,RMVar_hsa_circ_173211,RMVar_hsa_circ_15796,RMVar_hsa_circ_173212,RMVar_hsa_circ_277859,RMVar_hsa_circ_319765,RMVar_hsa_circ_343680,RMVar_hsa_circ_371105,RMVar_hsa_circ_325682,RMVar_hsa_circ_288122,RMVar_hsa_circ_79951,RMVar_hsa_circ_173217,RMVar_hsa_circ_173219,RMVar_hsa_circ_2218,RMVar_hsa_circ_173218,RMVar_hsa_circ_173216,RMVar_hsa_circ_173213,RMVar_hsa_circ_173214 39142 RMVar_ID_39142 Human_SNP_ID_581050332 A-to-I Human chr15 - 65697245 65697245 65697245 TTGTAGTTCCTGTAGGTATTGTTTAAGTTGATATTGTATAAAATTGAGAACTTATATTCATAGAA TTGTAGTTCCTGTAGGTATTGTTTAAGTTGATGTTGTATAAAATTGAGAACTTATATTCATAGAA T C DENND4A Ensembl:ENSG00000174485 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1257622646 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1506570,Human_RBP_ID_3479514,Human_RBP_ID_17605615,Human_RBP_ID_19067341 RMVar_hsa_circ_1902,RMVar_hsa_circ_6097,RMVar_hsa_circ_173209,RMVar_hsa_circ_32518,RMVar_hsa_circ_12376,RMVar_hsa_circ_173215,RMVar_hsa_circ_12416,RMVar_hsa_circ_66248,RMVar_hsa_circ_15796,RMVar_hsa_circ_343680,RMVar_hsa_circ_371105,RMVar_hsa_circ_325682,RMVar_hsa_circ_288122,RMVar_hsa_circ_79951,RMVar_hsa_circ_173217,RMVar_hsa_circ_2218,RMVar_hsa_circ_173216,RMVar_hsa_circ_173222,RMVar_hsa_circ_173213,RMVar_hsa_circ_173214,RMVar_hsa_circ_311092,RMVar_hsa_circ_173223,RMVar_hsa_circ_80987,RMVar_hsa_circ_275053,RMVar_hsa_circ_364862,RMVar_hsa_circ_117837,RMVar_hsa_circ_318997,RMVar_hsa_circ_323798,RMVar_hsa_circ_173224,RMVar_hsa_circ_367100,RMVar_hsa_circ_360035,RMVar_hsa_circ_352079,RMVar_hsa_circ_127806,RMVar_hsa_circ_68080,RMVar_hsa_circ_25231,RMVar_hsa_circ_56953,RMVar_hsa_circ_284962,RMVar_hsa_circ_173226,RMVar_hsa_circ_173227,RMVar_hsa_circ_323542,RMVar_hsa_circ_173225,RMVar_hsa_circ_321776,RMVar_hsa_circ_73840,RMVar_hsa_circ_280103,RMVar_hsa_circ_59105,RMVar_hsa_circ_173229,RMVar_hsa_circ_5975,RMVar_hsa_circ_37777,RMVar_hsa_circ_173230,RMVar_hsa_circ_173228 39143 RMVar_ID_39143 Human_SNP_ID_581050517 A-to-I Human chr15 - 65698089 65698089 65698089 TTCCTGGCTAATTTTTTTTATTTTTTATTTTTAGTAGAGATGAGGTCTCACTGTGTTGCCCAGGC TTCCTGGCTAATTTTTTTTATTTTTTATTTTTGGTAGAGATGAGGTCTCACTGTGTTGCCCAGGC T C DENND4A Ensembl:ENSG00000174485 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1451141885 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1902,RMVar_hsa_circ_6097,RMVar_hsa_circ_173209,RMVar_hsa_circ_32518,RMVar_hsa_circ_12376,RMVar_hsa_circ_173215,RMVar_hsa_circ_12416,RMVar_hsa_circ_66248,RMVar_hsa_circ_15796,RMVar_hsa_circ_343680,RMVar_hsa_circ_371105,RMVar_hsa_circ_288122,RMVar_hsa_circ_79951,RMVar_hsa_circ_2218,RMVar_hsa_circ_173216,RMVar_hsa_circ_173222,RMVar_hsa_circ_173213,RMVar_hsa_circ_173214,RMVar_hsa_circ_311092,RMVar_hsa_circ_173223,RMVar_hsa_circ_80987,RMVar_hsa_circ_275053,RMVar_hsa_circ_364862,RMVar_hsa_circ_117837,RMVar_hsa_circ_318997,RMVar_hsa_circ_173224,RMVar_hsa_circ_367100,RMVar_hsa_circ_360035,RMVar_hsa_circ_352079,RMVar_hsa_circ_127806,RMVar_hsa_circ_25231,RMVar_hsa_circ_15182,RMVar_hsa_circ_56953,RMVar_hsa_circ_284962,RMVar_hsa_circ_173226,RMVar_hsa_circ_173227,RMVar_hsa_circ_323542,RMVar_hsa_circ_173225,RMVar_hsa_circ_73840,RMVar_hsa_circ_280103,RMVar_hsa_circ_59105,RMVar_hsa_circ_173229,RMVar_hsa_circ_5975,RMVar_hsa_circ_37777,RMVar_hsa_circ_173230,RMVar_hsa_circ_65027,RMVar_hsa_circ_363483,RMVar_hsa_circ_27168 39144 RMVar_ID_39144 Human_SNP_ID_581065318 A-to-I Human chr15 - 65757061 65757061 65757061 TATATTTAAAAGCGTTTACTGAACGACTGTGCATTTATTTATTTATTTATTTATTTGAGATGGAG TATATTTAAAAGCGTTTACTGAACGACTGTGCGTTTATTTATTTATTTATTTATTTGAGATGGAG T C DENND4A Ensembl:ENSG00000174485 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs542411475 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6449966,Human_RBP_ID_23661189 RMVar_hsa_circ_173209,RMVar_hsa_circ_12376,RMVar_hsa_circ_288122,RMVar_hsa_circ_173222,RMVar_hsa_circ_173213,RMVar_hsa_circ_311092,RMVar_hsa_circ_360035,RMVar_hsa_circ_323542,RMVar_hsa_circ_325736,RMVar_hsa_circ_173239,RMVar_hsa_circ_270835,RMVar_hsa_circ_173240,RMVar_hsa_circ_329887,RMVar_hsa_circ_173273,RMVar_hsa_circ_282697,RMVar_hsa_circ_173254,RMVar_hsa_circ_173253,RMVar_hsa_circ_18561,RMVar_hsa_circ_173263,RMVar_hsa_circ_273222,RMVar_hsa_circ_109648,RMVar_hsa_circ_173264,RMVar_hsa_circ_22949,RMVar_hsa_circ_173271,RMVar_hsa_circ_276913,RMVar_hsa_circ_173275,RMVar_hsa_circ_277676 39145 RMVar_ID_39145 Human_SNP_ID_581066614 A-to-I Human chr15 - 65762593 65762593 65762593 ATAGAGCTTTACTCTGTTACCCAGGCTGGAGCACAGTGGTGTGATCAGGGCTCACTGCAGCCTCA ATAGAGCTTTACTCTGTTACCCAGGCTGGAGCGCAGTGGTGTGATCAGGGCTCACTGCAGCCTCA T C DENND4A Ensembl:ENSG00000174485 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs560500712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12559192 RMVar_hsa_circ_173263,RMVar_hsa_circ_109648 39146 RMVar_ID_39146 Human_SNP_ID_581066842 A-to-I Human chr15 - 65763559 65763559 65763559 CAATCCTCCCATCTCAGCCCCACCAAGGAGCTAGGACTACAGGACTGCACCACCAACACCTGGCT CAATCCTCCCATCTCAGCCCCACCAAGGAGCTGGGACTACAGGACTGCACCACCAACACCTGGCT T C DENND4A Ensembl:ENSG00000174485 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs922877052 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12559220 RMVar_hsa_circ_173263,RMVar_hsa_circ_109648 39147 RMVar_ID_39147 Human_SNP_ID_581068780 A-to-I Human chr15 + 65771618 65771618 65771618 TCTTTCCTCTTCTCTTTCATGTCCACTATGTCAATGCTGATGTTGTTGGCTATAACCAGCTCTTC TCTTTCCTCTTCTCTTTCATGTCCACTATGTCGATGCTGATGTTGTTGGCTATAACCAGCTCTTC A G RAB11A Ensembl:ENSG00000103769 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs929878432 Functional Loss SNV dbSNP153 33..33 33 - - - 39148 RMVar_ID_39148 Human_SNP_ID_581068787 A-to-I Human chr15 - 65771669 65771669 65771669 TATTTTTTGGGGGTGGATTTCCTTCAGGTAGTATACATTCTTTTTCAAATGGAAGAGCTGGTTAT TATTTTTTGGGGGTGGATTTCCTTCAGGTAGTGTACATTCTTTTTCAAATGGAAGAGCTGGTTAT T C DENND4A,AC011939.1 Ensembl:ENSG00000174485,Ensembl:ENSG00000259924 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs896113067 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1511744,Human_RBP_ID_6450076,Human_RBP_ID_9058801,Human_RBP_ID_9256618,Human_RBP_ID_12559371,Human_RBP_ID_22388427 RMVar_hsa_circ_173263,RMVar_hsa_circ_109648 39149 RMVar_ID_39149 Human_SNP_ID_581070861 A-to-I Human chr15 - 65779778 65779778 65779778 GGGCATGGTGGTATATGCCTGTAATCCCAGCTACTTGGCAGACTGAGGCACAAGAATTGCTTGAA GGGCATGGTGGTATATGCCTGTAATCCCAGCTGCTTGGCAGACTGAGGCACAAGAATTGCTTGAA T C DENND4A Ensembl:ENSG00000174485 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs957947708 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_173263,RMVar_hsa_circ_109648 39150 RMVar_ID_39150 Human_SNP_ID_581072252 A-to-I Human chr15 - 65785618 65785618 65785618 AAGCAAAAATGAAAAATGTTAATGCTTTATATATGAGTATGTGAGTGTATACTACATTTTTCGGT AAGCAAAAATGAAAAATGTTAATGCTTTATATGTGAGTATGTGAGTGTATACTACATTTTTCGGT T C DENND4A Ensembl:ENSG00000174485 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs773472787 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_173263,RMVar_hsa_circ_109648 39151 RMVar_ID_39151 Human_SNP_ID_581072253 A-to-I Human chr15 - 65785620 65785620 65785620 TGAAGCAAAAATGAAAAATGTTAATGCTTTATATATGAGTATGTGAGTGTATACTACATTTTTCG TGAAGCAAAAATGAAAAATGTTAATGCTTTATGTATGAGTATGTGAGTGTATACTACATTTTTCG T C DENND4A Ensembl:ENSG00000174485 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1353231563 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_173263,RMVar_hsa_circ_109648 39152 RMVar_ID_39152 Human_SNP_ID_581072262 A-to-I Human chr15 - 65785659 65785659 65785659 ACTATTATATACGTAGTTATTTTTTATTAAATATATATCTGAAGCAAAAATGAAAAATGTTAATG ACTATTATATACGTAGTTATTTTTTATTAAATGTATATCTGAAGCAAAAATGAAAAATGTTAATG T C DENND4A Ensembl:ENSG00000174485 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1412700420 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_173263,RMVar_hsa_circ_109648 39153 RMVar_ID_39153 Human_SNP_ID_581072545 A-to-I Human chr15 - 65787031 65787027 65787031 TTTTGCTTCAGATATATATTTAATTTAAAATAACTATTTATATCATAGTTATCACATTGAATTCT TTTTGCTTCAGATATATATTTAATTTAAAATA____TTTATATCATAGTTATCACATTGAATTCT ATAGT A DENND4A Ensembl:ENSG00000174485 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs754872883 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_173263,RMVar_hsa_circ_109648 39154 RMVar_ID_39154 Human_SNP_ID_581072566 A-to-I Human chr15 - 65787142 65787138 65787142 TTGTAATATTGTTTTGTAGATGAGAGATTTTTATTTTTGAAAAGTTTTAAAAATAAATAGCAAAA TTGTAATATTGTTTTGTAGATGAGAGATTTTT____TTGAAAAGTTTTAAAAATAAATAGCAAAA AAAAT A DENND4A Ensembl:ENSG00000174485 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1401728373 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_6450224,Human_RBP_ID_17563246 RMVar_hsa_circ_173263,RMVar_hsa_circ_109648 39155 RMVar_ID_39155 Human_SNP_ID_581073273 A-to-I Human chr15 - 65789944 65789944 65789944 GCCATGTTGCCCAGACTGGTTTTGAACTCGTGAGCCCAAGCAATCTGCCCGCCTTGGCCTCCCAA GCCATGTTGCCCAGACTGGTTTTGAACTCGTGCGCCCAAGCAATCTGCCCGCCTTGGCCTCCCAA T G DENND4A Ensembl:ENSG00000174485 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs527341616 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12559881 RMVar_hsa_circ_173263,RMVar_hsa_circ_109648 39156 RMVar_ID_39156 Human_SNP_ID_581073283 A-to-I Human chr15 - 65789973 65789973 65789973 AATTTTTGTATTTTTTGAGACGGGGTTTCGCCATGTTGCCCAGACTGGTTTTGAACTCGTGAGCC AATTTTTGTATTTTTTGAGACGGGGTTTCGCCTTGTTGCCCAGACTGGTTTTGAACTCGTGAGCC T A DENND4A Ensembl:ENSG00000174485 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934049207 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6450259,Human_RBP_ID_12559884 RMVar_hsa_circ_173263,RMVar_hsa_circ_109648 39157 RMVar_ID_39157 Human_SNP_ID_581183854 A-to-I Human chr15 - 66235426 66235426 66235426 ACCATCATGGCTCACTGCAGCCTCAACCTCCCAGGCTCAAGCAGTCCCCTCATCTCAGCCTCCCA ACCATCATGGCTCACTGCAGCCTCAACCTCCCGGGCTCAAGCAGTCCCCTCATCTCAGCCTCCCA T C MEGF11 Ensembl:ENSG00000157890 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1242208282 Functional Loss SNV dbSNP153 33..33 33 - - - 39158 RMVar_ID_39158 Human_SNP_ID_581198702 A-to-I Human chr15 + 66296721 66296721 66296721 AATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGTCAGACTTGTGTTGAACTCCTTA AATTTTTGTATTTTTAGTAGAGATGGGGTTTCGCCATGTTGGTCAGACTTGTGTTGAACTCCTTA A G DIS3L Ensembl:ENSG00000166938 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1291885473 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12167,RMVar_hsa_circ_299681,RMVar_hsa_circ_348080,RMVar_hsa_circ_366556,RMVar_hsa_circ_368559,RMVar_hsa_circ_345765,RMVar_hsa_circ_50371 39159 RMVar_ID_39159 Human_SNP_ID_581207518 A-to-I Human chr15 - 66333607 66333607 66333607 CTCCTGCTTCAGCCTCCCAAGTAGCTGGGACTACAGGCGCATGCCACCACGCCGGGCTAATTTTT CTCCTGCTTCAGCCTCCCAAGTAGCTGGGACTGCAGGCGCATGCCACCACGCCGGGCTAATTTTT T C lnc-TIPIN-4 RNACentral:URS0000D5DFC5 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs566106818 Functional Loss SNV dbSNP153 33..33 33 - - - 39160 RMVar_ID_39160 Human_SNP_ID_581207527 A-to-I Human chr15 + 66333654 66333654 66333654 GGGAGGCTGAAGCAGGAGAATTGCCTGAACCCAGGAAGAGGAGGTTGCAGTGAGCCGAGATCGCA GGGAGGCTGAAGCAGGAGAATTGCCTGAACCCGGGAAGAGGAGGTTGCAGTGAGCCGAGATCGCA A G DIS3L Ensembl:ENSG00000166938 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs890337264 Functional Loss SNV dbSNP153 33..33 33 - - - 39161 RMVar_ID_39161 Human_SNP_ID_581207528 A-to-I Human chr15 + 66333654 66333654 66333654 GGGAGGCTGAAGCAGGAGAATTGCCTGAACCCAGGAAGAGGAGGTTGCAGTGAGCCGAGATCGCA GGGAGGCTGAAGCAGGAGAATTGCCTGAACCCTGGAAGAGGAGGTTGCAGTGAGCCGAGATCGCA A T DIS3L Ensembl:ENSG00000166938 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs890337264 Functional Loss SNV dbSNP153 33..33 33 - - - 39162 RMVar_ID_39162 Human_SNP_ID_581207706 A-to-I Human chr15 - 66334381 66334381 66334381 GGATTACAGGCATGAGCTACTGTCCCTGGCCAATTTTTGTATTTTTAGTAGAGATGGGGTTTAAT GGATTACAGGCATGAGCTACTGTCCCTGGCCAGTTTTTGTATTTTTAGTAGAGATGGGGTTTAAT T C lnc-TIPIN-4 RNACentral:URS0000D5DFC5 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917146701 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12561062 39163 RMVar_ID_39163 Human_SNP_ID_581208230 A-to-I Human chr15 - 66336388 66336388 66336388 CACCACGCTTGGCTAATTTTTGTACTTTTAGTAGAGATGAGGTTTCACCATGTTGGCCAGGCTGG CACCACGCTTGGCTAATTTTTGTACTTTTAGTTGAGATGAGGTTTCACCATGTTGGCCAGGCTGG T A TIPIN Ensembl:ENSG00000075131 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs911885378 Functional Loss SNV dbSNP153 33..33 33 - - - 39164 RMVar_ID_39164 Human_SNP_ID_581208775 A-to-I Human chr15 - 66338156 66338156 66338156 CGCCTCCTAGGTTCAAGCGATTCTCCTGTCCCAGCCTCCCGAGTAGCTGGGATTACAGGCGTGCT CGCCTCCTAGGTTCAAGCGATTCTCCTGTCCCGGCCTCCCGAGTAGCTGGGATTACAGGCGTGCT T C TIPIN Ensembl:ENSG00000075131 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1439380015 Functional Loss SNV dbSNP153 33..33 33 - - - 39165 RMVar_ID_39165 Human_SNP_ID_581211739 A-to-I Human chr15 - 66349750 66349750 66349750 TCAGCCACCTGAGTAGCTGGGTCCACAGGTGTACACCACCATGCCTGGCTATTGTTTTGTATTTT TCAGCCACCTGAGTAGCTGGGTCCACAGGTGTGCACCACCATGCCTGGCTATTGTTTTGTATTTT T C TIPIN Ensembl:ENSG00000075131 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs761173863 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_339734,RMVar_hsa_circ_310820,RMVar_hsa_circ_341149,RMVar_hsa_circ_298879,RMVar_hsa_circ_173291,RMVar_hsa_circ_173292 39166 RMVar_ID_39166 Human_SNP_ID_581218754 A-to-I Human chr15 - 66375985 66375985 66375985 GTGATCCTCTTGCCTTAGCCTCCCCAATAGCTAGGACTACAGGCGTGCGCCGCCGTGACTGGCTA GTGATCCTCTTGCCTTAGCCTCCCCAATAGCTGGGACTACAGGCGTGCGCCGCCGTGACTGGCTA T C TIPIN Ensembl:ENSG00000075131 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs940342190 Functional Loss SNV dbSNP153 33..33 33 - - - 39167 RMVar_ID_39167 Human_SNP_ID_581221434 A-to-I Human chr15 - 66386232 66386232 66386232 CCTGGAGTGTAGTGGCGCGATCTCCGCTAACTACCACCTCTGCCTCCCACGTTCAAGCGATTCTC CCTGGAGTGTAGTGGCGCGATCTCCGCTAACTGCCACCTCTGCCTCCCACGTTCAAGCGATTCTC T C TIPIN Ensembl:ENSG00000075131 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1300539838 Functional Loss SNV dbSNP153 33..33 33 - - - 39168 RMVar_ID_39168 Human_SNP_ID_581240746 A-to-I Human chr15 + 66457715 66457715 66457715 AAACTATGGTGGCTGTAGCCTGTAATCCCAGCACTTTGGGAGATCAAGGCGGGTGGATCACCTCA AAACTATGGTGGCTGTAGCCTGTAATCCCAGCGCTTTGGGAGATCAAGGCGGGTGGATCACCTCA A G MAP2K1 Ensembl:ENSG00000169032 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1331385815 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 39169 RMVar_ID_39169 Human_SNP_ID_581243313 A-to-I Human chr15 + 66467702 66467702 66467702 CCTGCCTCAGCTTTCTCAGTAACTGGGATTACAGGTGCCTGCCACCACGCCCAACTAATTTTTGT CCTGCCTCAGCTTTCTCAGTAACTGGGATTACGGGTGCCTGCCACCACGCCCAACTAATTTTTGT A G MAP2K1 Ensembl:ENSG00000169032 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs949268249 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 39170 RMVar_ID_39170 Human_SNP_ID_581244974 A-to-I Human chr15 + 66473795 66473795 66473795 TGCTTCCCGGGTTCAATGAGTTCTCATGCCTCAGCCTCCTGAGTAGCTGGGACTACCGGTGCACA TGCTTCCCGGGTTCAATGAGTTCTCATGCCTCGGCCTCCTGAGTAGCTGGGACTACCGGTGCACA A G MAP2K1 Ensembl:ENSG00000169032 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1288419454 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 39171 RMVar_ID_39171 Human_SNP_ID_581250993 A-to-I Human chr15 - 66496598 66496598 66496598 GATGGCCAAAGTCCAGGTGGTCAAAGCTGTAGAGAGCCCAGATTGTGCCACTGCACTCCAGCATG GATGGCCAAAGTCCAGGTGGTCAAAGCTGTAGGGAGCCCAGATTGTGCCACTGCACTCCAGCATG T C SNAPC5 Ensembl:ENSG00000174446 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1195760286 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12562580 39172 RMVar_ID_39172 Human_SNP_ID_581251012 A-to-I Human chr15 - 66496661 66496661 66496661 AAAATTAGCTGAGCGTGGTGGTGCGTGCCTGTAGTCCAGCTACTTGGGAAACTGAGGTGGGAGGA AAAATTAGCTGAGCGTGGTGGTGCGTGCCTGTGGTCCAGCTACTTGGGAAACTGAGGTGGGAGGA T C SNAPC5 Ensembl:ENSG00000174446 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935267032 Functional Loss SNV dbSNP153 33..33 33 - - - 39173 RMVar_ID_39173 Human_SNP_ID_581252423 A-to-I Human chr15 - 66500363 66500363 66500363 TCAATCTTTTCCCTTTCAGTCTTCCCATGCACAAGATGATTAATACAGATCTTAGCAGAATCTTG TCAATCTTTTCCCTTTCAGTCTTCCCATGCACGAGATGATTAATACAGATCTTAGCAGAATCTTG T C RPL4 Ensembl:ENSG00000174444 Protein coding CDS GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1567034109 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_886571,Human_RBP_ID_1506802,Human_RBP_ID_17252006,Human_RBP_ID_17484546,Human_RBP_ID_19068420,Human_RBP_ID_25156142 Human_Splice_Rec_1616068,Human_Splice_Rec_1616069,Human_Splice_Rec_1616082,Human_Splice_Rec_1616083,Human_Splice_Rec_1616104,Human_Splice_Rec_1616105,Human_Splice_Rec_1616120,Human_Splice_Rec_1616121,Human_Splice_Rec_1616135,Human_Splice_Rec_1616142,Human_Splice_Rec_1616143,Human_Splice_Rec_1616148,Human_Splice_Rec_1616149 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_59010,RMVar_hsa_circ_92016,RMVar_hsa_circ_173312 39174 RMVar_ID_39174 Human_SNP_ID_581259241 A-to-I Human chr15 + 66521996 66521996 66521996 CTGAGGAGGATGGATCACGGGGTCAGGAGTTCAAGACCAGCCTGACGAATATGGTGAAACCCTGT CTGAGGAGGATGGATCACGGGGTCAGGAGTTCCAGACCAGCCTGACGAATATGGTGAAACCCTGT A C ZWILCH Ensembl:ENSG00000174442 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs566688843 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17602,RMVar_hsa_circ_30570,RMVar_hsa_circ_2256,RMVar_hsa_circ_19773,RMVar_hsa_circ_173323,RMVar_hsa_circ_29041,RMVar_hsa_circ_348328,RMVar_hsa_circ_329279,RMVar_hsa_circ_38973,RMVar_hsa_circ_6627,RMVar_hsa_circ_48525,RMVar_hsa_circ_173326,RMVar_hsa_circ_275181,RMVar_hsa_circ_26274,RMVar_hsa_circ_322773,RMVar_hsa_circ_52221,RMVar_hsa_circ_57566,RMVar_hsa_circ_325309,RMVar_hsa_circ_33515,RMVar_hsa_circ_59005,RMVar_hsa_circ_31944,RMVar_hsa_circ_21771,RMVar_hsa_circ_79530,RMVar_hsa_circ_372143,RMVar_hsa_circ_173328,RMVar_hsa_circ_173329 39175 RMVar_ID_39175 Human_SNP_ID_581259506 A-to-I Human chr15 + 66522970 66522970 66522970 TCAGCCTCCTGAATAGCTGGGATTACAGGGGCATGCCACTAAACCTGGCTAATTTTTGTAAGTTT TCAGCCTCCTGAATAGCTGGGATTACAGGGGCGTGCCACTAAACCTGGCTAATTTTTGTAAGTTT A G ZWILCH Ensembl:ENSG00000174442 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6494578 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_4593,GWAS_ID_4594,GWAS_ID_4595,GWAS_ID_4596,GWAS_ID_4597,GWAS_ID_4598,GWAS_ID_4599,GWAS_ID_4600,GWAS_ID_4601,GWAS_ID_4602,GWAS_ID_4603,GWAS_ID_4604,GWAS_ID_4605,GWAS_ID_4606,GWAS_ID_4607,GWAS_ID_4608,GWAS_ID_4609,GWAS_ID_4610,GWAS_ID_4611,GWAS_ID_4612,GWAS_ID_4613,GWAS_ID_4614,GWAS_ID_4615,GWAS_ID_4616,GWAS_ID_4617,GWAS_ID_4618,GWAS_ID_4619,GWAS_ID_4620,GWAS_ID_4621,GWAS_ID_4622,GWAS_ID_4623,GWAS_ID_4624,GWAS_ID_4625,GWAS_ID_4626,GWAS_ID_4627,GWAS_ID_4628,GWAS_ID_4629,GWAS_ID_4630,GWAS_ID_4631,GWAS_ID_4632,GWAS_ID_4633,GWAS_ID_4634,GWAS_ID_4635,GWAS_ID_4636,GWAS_ID_4637,GWAS_ID_4638,GWAS_ID_4639,GWAS_ID_4640,GWAS_ID_4641,GWAS_ID_4642,GWAS_ID_4643,GWAS_ID_4644,GWAS_ID_4645,GWAS_ID_4646 RMVar_hsa_circ_17602,RMVar_hsa_circ_30570,RMVar_hsa_circ_2256,RMVar_hsa_circ_19773,RMVar_hsa_circ_173323,RMVar_hsa_circ_29041,RMVar_hsa_circ_348328,RMVar_hsa_circ_329279,RMVar_hsa_circ_38973,RMVar_hsa_circ_6627,RMVar_hsa_circ_48525,RMVar_hsa_circ_173326,RMVar_hsa_circ_275181,RMVar_hsa_circ_26274,RMVar_hsa_circ_322773,RMVar_hsa_circ_52221,RMVar_hsa_circ_57566,RMVar_hsa_circ_325309,RMVar_hsa_circ_33515,RMVar_hsa_circ_59005,RMVar_hsa_circ_31944,RMVar_hsa_circ_21771,RMVar_hsa_circ_79530,RMVar_hsa_circ_372143,RMVar_hsa_circ_173328,RMVar_hsa_circ_173329 39176 RMVar_ID_39176 Human_SNP_ID_581397240 A-to-I Human chr15 + 67069805 67069805 67069805 CTTAGCTCACTGCAACCTCTGCCTCCCGGTTCAAGCGATTCTTGTGCCTCAGCCTCCCGAGTAGC CTTAGCTCACTGCAACCTCTGCCTCCCGGTTCGAGCGATTCTTGTGCCTCAGCCTCCCGAGTAGC A G SMAD3 Ensembl:ENSG00000166949 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1303086342 Functional Loss SNV dbSNP153 33..33 33 - - - 39177 RMVar_ID_39177 Human_SNP_ID_581432291 A-to-I Human chr15 - 67210332 67210332 67210332 TTTTGTAATTTTAGTAGAGACAAGGCTTCACCATGTTGATCAGGCTGGTCTTGAACTCCTGACCT TTTTGTAATTTTAGTAGAGACAAGGCTTCACCGTGTTGATCAGGCTGGTCTTGAACTCCTGACCT T C AAGAB Ensembl:ENSG00000103591 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904813406 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80143,RMVar_hsa_circ_274896,RMVar_hsa_circ_173357,RMVar_hsa_circ_173359 39178 RMVar_ID_39178 Human_SNP_ID_581435986 A-to-I Human chr15 - 67226046 67226046 67226046 ACCACTTCACACTTACTAGGATGGCTAGGGTCAGAAAGATAATAACAAATGTTGGTGAGGATATG ACCACTTCACACTTACTAGGATGGCTAGGGTCGGAAAGATAATAACAAATGTTGGTGAGGATATG T C AAGAB Ensembl:ENSG00000103591 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1291928356 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12565257 RMVar_hsa_circ_80143,RMVar_hsa_circ_274896,RMVar_hsa_circ_173357,RMVar_hsa_circ_173359 39179 RMVar_ID_39179 Human_SNP_ID_581437116 A-to-I Human chr15 - 67231188 67231188 67231188 CATCTCCATAAAAATTAGCTGGGCATGGTGGTATGTGCCTGTGGTCCCTGCTACTTGGGAAACTG CATCTCCATAAAAATTAGCTGGGCATGGTGGTGTGTGCCTGTGGTCCCTGCTACTTGGGAAACTG T C AAGAB Ensembl:ENSG00000103591 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs940764892 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25156846 RMVar_hsa_circ_80143,RMVar_hsa_circ_274896,RMVar_hsa_circ_173357,RMVar_hsa_circ_173359,RMVar_hsa_circ_122224,RMVar_hsa_circ_173360 39180 RMVar_ID_39180 Human_SNP_ID_581503230 A-to-I Human chr15 + 67525907 67525907 67525907 GTGGTGGCGCGCGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACCCA GTGGTGGCGCGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCA A G C15orf61 Ensembl:ENSG00000189227 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1336906213 Functional Loss SNV dbSNP153 33..33 33 - - - 39181 RMVar_ID_39181 Human_SNP_ID_581513054 A-to-I Human chr15 + 67568926 67568926 67568926 TACTCGGGAGGCTGAGGCAGGAGAATTGCTTGAACCCGGGAGGCAGAGGTTGCAGTCAGCCGAGA TACTCGGGAGGCTGAGGCAGGAGAATTGCTTGGACCCGGGAGGCAGAGGTTGCAGTCAGCCGAGA A G MAP2K5 Ensembl:ENSG00000137764 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs962645575 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60462,RMVar_hsa_circ_173373,RMVar_hsa_circ_124636,RMVar_hsa_circ_371878,RMVar_hsa_circ_315926,RMVar_hsa_circ_119077,RMVar_hsa_circ_173375,RMVar_hsa_circ_173376,RMVar_hsa_circ_341176,RMVar_hsa_circ_348424,RMVar_hsa_circ_308871,RMVar_hsa_circ_173378,RMVar_hsa_circ_173379,RMVar_hsa_circ_173377 39182 RMVar_ID_39182 Human_SNP_ID_581591366 A-to-I Human chr15 - 67904225 67904225 67904225 AAATTGGCTGGGCATGGTGGAGGGTGCCTGTGATCCCAGCTACATGAGAGGCTGAGGCAGGAGAG AAATTGGCTGGGCATGGTGGAGGGTGCCTGTGTTCCCAGCTACATGAGAGGCTGAGGCAGGAGAG T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223245408 Functional Loss SNV dbSNP153 33..33 33 - - - 39183 RMVar_ID_39183 Human_SNP_ID_581631686 A-to-I Human chr15 + 68059523 68059523 68059523 CACGAGGTCAGGAGTTGAAGACCAGCCTGACCAAGATAGTGAAACCCCGTCTCTACTAAAAATAC CACGAGGTCAGGAGTTGAAGACCAGCCTGACCGAGATAGTGAAACCCCGTCTCTACTAAAAATAC A G PIAS1 Ensembl:ENSG00000033800 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1336117831 Functional Loss SNV dbSNP153 33..33 33 - - - 39184 RMVar_ID_39184 Human_SNP_ID_581633952 A-to-I Human chr15 + 68068240 68068240 68068240 ACAAAAAAATACAAAAAGTAGCTGGCTGAGGCATGTGCCTGTGGCCCAGCTACTTGGGAGGCTGA ACAAAAAAATACAAAAAGTAGCTGGCTGAGGCGTGTGCCTGTGGCCCAGCTACTTGGGAGGCTGA A G PIAS1 Ensembl:ENSG00000033800 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1173526881 Functional Loss SNV dbSNP153 33..33 33 - - - 39185 RMVar_ID_39185 Human_SNP_ID_581633953 A-to-I Human chr15 + 68068240 68068240 68068240 ACAAAAAAATACAAAAAGTAGCTGGCTGAGGCATGTGCCTGTGGCCCAGCTACTTGGGAGGCTGA ACAAAAAAATACAAAAAGTAGCTGGCTGAGGCTTGTGCCTGTGGCCCAGCTACTTGGGAGGCTGA A T PIAS1 Ensembl:ENSG00000033800 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1173526881 Functional Loss SNV dbSNP153 33..33 33 - - - 39186 RMVar_ID_39186 Human_SNP_ID_581634018 A-to-I Human chr15 + 68068508 68068508 68068508 AGTTTGCACTCCTGTCACCCAGGTTGGAGTACAATGGCGCTATCTCGGCTCACTGCAACCTCTGC AGTTTGCACTCCTGTCACCCAGGTTGGAGTACGATGGCGCTATCTCGGCTCACTGCAACCTCTGC A G PIAS1 Ensembl:ENSG00000033800 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs984362670 Functional Loss SNV dbSNP153 33..33 33 - - - 39187 RMVar_ID_39187 Human_SNP_ID_581636074 A-to-I Human chr15 + 68075800 68075800 68075800 GAATCATTCCTAGGGCTTTTTTTTTTTTTTTTAAGATGGAGTTTTACTCTGCTGCGCAGGCTGGA GAATCATTCCTAGGGCTTTTTTTTTTTTTTTTTAGATGGAGTTTTACTCTGCTGCGCAGGCTGGA A T PIAS1 Ensembl:ENSG00000033800 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1385590885 Functional Loss SNV dbSNP153 33..33 33 - - - 39188 RMVar_ID_39188 Human_SNP_ID_581646656 A-to-I Human chr15 + 68118222 68118222 68118222 GTGCACCTGTAGTCCCAGCTACTCTGGAGGCTAAGACATGAGAATCACTTGAACCTGGGAGGTGA GTGCACCTGTAGTCCCAGCTACTCTGGAGGCTGAGACATGAGAATCACTTGAACCTGGGAGGTGA A G PIAS1 Ensembl:ENSG00000033800 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs912294678 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17563268 RMVar_hsa_circ_45711,RMVar_hsa_circ_363121,RMVar_hsa_circ_352748,RMVar_hsa_circ_282837,RMVar_hsa_circ_13244 39189 RMVar_ID_39189 Human_SNP_ID_581646662 A-to-I Human chr15 + 68118241 68118241 68118241 TACTCTGGAGGCTAAGACATGAGAATCACTTGAACCTGGGAGGTGAAAGTTGCAGTGAGCCAAGA TACTCTGGAGGCTAAGACATGAGAATCACTTGGACCTGGGAGGTGAAAGTTGCAGTGAGCCAAGA A G PIAS1 Ensembl:ENSG00000033800 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs376520323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17563268 RMVar_hsa_circ_45711,RMVar_hsa_circ_363121,RMVar_hsa_circ_352748,RMVar_hsa_circ_282837,RMVar_hsa_circ_13244 39190 RMVar_ID_39190 Human_SNP_ID_581646747 A-to-I Human chr15 + 68118471 68118471 68118471 TGATCCTCCTGCCTTAGCCTCCCAAGTTGCTGAGACTATAGGCATGCACCACCATGCCCTGCTAA TGATCCTCCTGCCTTAGCCTCCCAAGTTGCTGTGACTATAGGCATGCACCACCATGCCCTGCTAA A T PIAS1 Ensembl:ENSG00000033800 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs919742640 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45711,RMVar_hsa_circ_363121,RMVar_hsa_circ_352748,RMVar_hsa_circ_282837,RMVar_hsa_circ_13244 39191 RMVar_ID_39191 Human_SNP_ID_581668462 A-to-I Human chr15 - 68202388 68202388 68202388 TTGTCCAGGCTGGTCTCGAACTCCTGGGCCCAAGCGATACTCCTGTCTCACCCTCCCAAAGTGCT TTGTCCAGGCTGGTCTCGAACTCCTGGGCCCAGGCGATACTCCTGTCTCACCCTCCCAAAGTGCT T C AC107871.1,CALML4 Ensembl:ENSG00000260007,Ensembl:ENSG00000129007 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1212499482 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4330183 39192 RMVar_ID_39192 Human_SNP_ID_581672875 A-to-I Human chr15 - 68217692 68217692 68217692 CCTGACGGGCCACAGTCATAGAGCCAAAAGATATGAAGGCATCCAGGCCTATACTCTCAGTTTAC CCTGACGGGCCACAGTCATAGAGCCAAAAGATGTGAAGGCATCCAGGCCTATACTCTCAGTTTAC T C AC107871.1,CLN6 Ensembl:ENSG00000260007,Ensembl:ENSG00000128973 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs746234334 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25158680 RMVar_hsa_circ_302887,RMVar_hsa_circ_173421,RMVar_hsa_circ_90064,RMVar_hsa_circ_272405,RMVar_hsa_circ_173422,RMVar_hsa_circ_173423,RMVar_hsa_circ_324509,RMVar_hsa_circ_97378,RMVar_hsa_circ_173424 39193 RMVar_ID_39193 Human_SNP_ID_581673087 A-to-I Human chr15 - 68218458 68218458 68218458 CTTAGTGTGGCTTGAATTTGCCGAGTGACCTTAGACAAGTCACTTCTCCTTTATCTCCTAGTAAA CTTAGTGTGGCTTGAATTTGCCGAGTGACCTTCGACAAGTCACTTCTCCTTTATCTCCTAGTAAA T G AC107871.1,CLN6 Ensembl:ENSG00000260007,Ensembl:ENSG00000128973 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1291153352 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_302887,RMVar_hsa_circ_173421,RMVar_hsa_circ_90064,RMVar_hsa_circ_272405,RMVar_hsa_circ_173422,RMVar_hsa_circ_173423,RMVar_hsa_circ_324509,RMVar_hsa_circ_97378,RMVar_hsa_circ_173424 39194 RMVar_ID_39194 Human_SNP_ID_581675199 A-to-I Human chr15 - 68225907 68225907 68225907 AGAGTGCAGTGGTGCCATCTTGGCTCACTGCAACCTCCACCTCCAGAGTTCAAGCAATTCTGCCT AGAGTGCAGTGGTGCCATCTTGGCTCACTGCACCCTCCACCTCCAGAGTTCAAGCAATTCTGCCT T G AC107871.1,CLN6 Ensembl:ENSG00000260007,Ensembl:ENSG00000128973 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1212661982 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90064,RMVar_hsa_circ_173423,RMVar_hsa_circ_97378,RMVar_hsa_circ_173424 39195 RMVar_ID_39195 Human_SNP_ID_581675233 A-to-I Human chr15 - 68226063 68226063 68226063 CACCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCCTGAGCCACCGCGCCCAGCCAAGTCCA CACCCGCCTCAGCCTCCCAAAGTGCTGGGATTGCAGGCCTGAGCCACCGCGCCCAGCCAAGTCCA T C AC107871.1,CLN6 Ensembl:ENSG00000260007,Ensembl:ENSG00000128973 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1368553227 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90064,RMVar_hsa_circ_173423,RMVar_hsa_circ_97378,RMVar_hsa_circ_173424 39196 RMVar_ID_39196 Human_SNP_ID_581825640 A-to-I Human chr15 + 68832016 68832016 68832016 TGGGGTTTTGCCATGTTGGCCAGGCTGGTCTCAAACTCCTGACCTCAGGTGATCCACCTGCCTTG TGGGGTTTTGCCATGTTGGCCAGGCTGGTCTCCAACTCCTGACCTCAGGTGATCCACCTGCCTTG A C SPESP1 Ensembl:ENSG00000258484 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1447975117 Functional Loss SNV dbSNP153 33..33 33 - - - 39197 RMVar_ID_39197 Human_SNP_ID_581962289 A-to-I Human chr15 + 69407216 69407216 69407216 TGGAGTGTAGTGTTGCAATCTTGGCTCACTGCAACCTCTGCCTGACAGGCTTCAGTGATCTTTCC TGGAGTGTAGTGTTGCAATCTTGGCTCACTGCCACCTCTGCCTGACAGGCTTCAGTGATCTTTCC A C PAQR5 Ensembl:ENSG00000137819 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1398383775 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2225568,Human_miRNA_ID_2273369 RMVar_hsa_circ_91134,RMVar_hsa_circ_173453,RMVar_hsa_circ_103699,RMVar_hsa_circ_173467 39198 RMVar_ID_39198 Human_SNP_ID_581962306 A-to-I Human chr15 + 69407329 69407328 69407329 TGGCTAACTTTTTGTAGAGATAGGGTTTTGCCATGCTGCCCAGGCTGGCTTAGAATTCCTGAATT TGGCTAACTTTTTGTAGAGATAGGGTTTTGCC_TGCTGCCCAGGCTGGCTTAGAATTCCTGAATT CA C PAQR5 Ensembl:ENSG00000137819 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1360434493 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_91134,RMVar_hsa_circ_173453,RMVar_hsa_circ_103699,RMVar_hsa_circ_173467 39199 RMVar_ID_39199 Human_SNP_ID_582265935 A-to-I Human chr15 - 70660162 70660162 70660162 AAGTAATTGCAATTTATCGGACACACCTTCTTAGTGCTGCACAGGTAAAGAACTACTTCTCCTTT AAGTAATTGCAATTTATCGGACACACCTTCTTCGTGCTGCACAGGTAAAGAACTACTTCTCCTTT T G UACA Ensembl:ENSG00000137831 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1487612749 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_467776 Human_Splice_Rec_1620222,Human_Splice_Rec_1620223,Human_Splice_Rec_1620258,Human_Splice_Rec_1620259,Human_Splice_Rec_1620294,Human_Splice_Rec_1620295,Human_Splice_Rec_1620297,Human_Splice_Rec_1620300,Human_Splice_Rec_1620301,Human_Splice_Rec_1620330,Human_Splice_Rec_1620331 RMVar_hsa_circ_111321,RMVar_hsa_circ_173494,RMVar_hsa_circ_376584,RMVar_hsa_circ_378146,RMVar_hsa_circ_128063,RMVar_hsa_circ_173493,RMVar_hsa_circ_118467,RMVar_hsa_circ_173496,RMVar_hsa_circ_173498,RMVar_hsa_circ_94563,RMVar_hsa_circ_173497,RMVar_hsa_circ_173495 39200 RMVar_ID_39200 Human_SNP_ID_582269344 A-to-I Human chr15 - 70672902 70672902 70672902 TTAGTAGAGACGGGGTTTCACTATGTTGGCCAAGCTGGTCTTGAACTCCTGACCTCAGGCAATCC TTAGTAGAGACGGGGTTTCACTATGTTGGCCATGCTGGTCTTGAACTCCTGACCTCAGGCAATCC T A UACA Ensembl:ENSG00000137831 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs541150024 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_128063,RMVar_hsa_circ_118467,RMVar_hsa_circ_12622,RMVar_hsa_circ_173496,RMVar_hsa_circ_173495 39201 RMVar_ID_39201 Human_SNP_ID_582273929 A-to-I Human chr15 - 70692302 70692302 70692302 AACAAATTAGCTGCACATGGTGGCACGAGCCTATAGTCCCTGTTACTCTGGAAGCTGAGCTGTGA AACAAATTAGCTGCACATGGTGGCACGAGCCTGTAGTCCCTGTTACTCTGGAAGCTGAGCTGTGA T C UACA Ensembl:ENSG00000137831 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs376355261 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1175540,Human_RBP_ID_3481205,Human_RBP_ID_22473585 RMVar_hsa_circ_128063,RMVar_hsa_circ_12622,RMVar_hsa_circ_173495,RMVar_hsa_circ_347063,RMVar_hsa_circ_59951,RMVar_hsa_circ_49233,RMVar_hsa_circ_173501,RMVar_hsa_circ_367653,RMVar_hsa_circ_173504,RMVar_hsa_circ_35619,RMVar_hsa_circ_300399,RMVar_hsa_circ_282775,RMVar_hsa_circ_349172,RMVar_hsa_circ_173505,RMVar_hsa_circ_173506,RMVar_hsa_circ_173510,RMVar_hsa_circ_113896,RMVar_hsa_circ_306544,RMVar_hsa_circ_364776,RMVar_hsa_circ_173509,RMVar_hsa_circ_306307,RMVar_hsa_circ_173512,RMVar_hsa_circ_173513 39202 RMVar_ID_39202 Human_SNP_ID_582273993 A-to-I Human chr15 - 70692587 70692587 70692587 TTTTATATGTTTTGTAGAGATGGGATTTCACTATGTTGCCCACGCTGGTCTCAACTCCCAGGCTC TTTTATATGTTTTGTAGAGATGGGATTTCACTGTGTTGCCCACGCTGGTCTCAACTCCCAGGCTC T C UACA Ensembl:ENSG00000137831 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs926780107 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6456777,Human_RBP_ID_22473586 RMVar_hsa_circ_128063,RMVar_hsa_circ_12622,RMVar_hsa_circ_173495,RMVar_hsa_circ_347063,RMVar_hsa_circ_59951,RMVar_hsa_circ_49233,RMVar_hsa_circ_173501,RMVar_hsa_circ_367653,RMVar_hsa_circ_173504,RMVar_hsa_circ_35619,RMVar_hsa_circ_300399,RMVar_hsa_circ_282775,RMVar_hsa_circ_349172,RMVar_hsa_circ_173505,RMVar_hsa_circ_173506,RMVar_hsa_circ_173510,RMVar_hsa_circ_113896,RMVar_hsa_circ_306544,RMVar_hsa_circ_364776,RMVar_hsa_circ_173509,RMVar_hsa_circ_306307,RMVar_hsa_circ_173512,RMVar_hsa_circ_173513 39203 RMVar_ID_39203 Human_SNP_ID_582458358 A-to-I Human chr15 + 71475667 71475667 71475667 AATGGCGGCCAGGCGTGGTGGCTCATGCCTTTAGTCTTAGTGCTTTGGGAGCTTGAGGCGGGAAG AATGGCGGCCAGGCGTGGTGGCTCATGCCTTTGGTCTTAGTGCTTTGGGAGCTTGAGGCGGGAAG A G THSD4 Ensembl:ENSG00000187720 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs536721827 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79631,RMVar_hsa_circ_85610,RMVar_hsa_circ_126423,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_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_94657,RMVar_hsa_circ_100018,RMVar_hsa_circ_173561,RMVar_hsa_circ_173562,RMVar_hsa_circ_115334,RMVar_hsa_circ_84370,RMVar_hsa_circ_173565,RMVar_hsa_circ_173566,RMVar_hsa_circ_173567,RMVar_hsa_circ_275838,RMVar_hsa_circ_122323,RMVar_hsa_circ_173571,RMVar_hsa_circ_23188,RMVar_hsa_circ_78515,RMVar_hsa_circ_173572,RMVar_hsa_circ_173573,RMVar_hsa_circ_173570 39204 RMVar_ID_39204 Human_SNP_ID_582500663 A-to-I Human chr15 + 71639124 71639124 71639124 CCAGAACTAGTCACATGGCCAGACCTAACTTCAGAAGGTTGGAGAATTGTAATCCTCCATGTACC CCAGAACTAGTCACATGGCCAGACCTAACTTCCGAAGGTTGGAGAATTGTAATCCTCCATGTACC A C THSD4 Ensembl:ENSG00000187720 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs558805015 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79631,RMVar_hsa_circ_85610,RMVar_hsa_circ_126423,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_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_94657,RMVar_hsa_circ_100018,RMVar_hsa_circ_173561,RMVar_hsa_circ_173562,RMVar_hsa_circ_115334,RMVar_hsa_circ_84370,RMVar_hsa_circ_173565,RMVar_hsa_circ_173566,RMVar_hsa_circ_173567,RMVar_hsa_circ_275838,RMVar_hsa_circ_122323,RMVar_hsa_circ_173571,RMVar_hsa_circ_23188,RMVar_hsa_circ_78515,RMVar_hsa_circ_173572,RMVar_hsa_circ_173573,RMVar_hsa_circ_173570 39205 RMVar_ID_39205 Human_SNP_ID_582500664 A-to-I Human chr15 + 71639124 71639124 71639124 CCAGAACTAGTCACATGGCCAGACCTAACTTCAGAAGGTTGGAGAATTGTAATCCTCCATGTACC CCAGAACTAGTCACATGGCCAGACCTAACTTCGGAAGGTTGGAGAATTGTAATCCTCCATGTACC A G THSD4 Ensembl:ENSG00000187720 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs558805015 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79631,RMVar_hsa_circ_85610,RMVar_hsa_circ_126423,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_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_94657,RMVar_hsa_circ_100018,RMVar_hsa_circ_173561,RMVar_hsa_circ_173562,RMVar_hsa_circ_115334,RMVar_hsa_circ_84370,RMVar_hsa_circ_173565,RMVar_hsa_circ_173566,RMVar_hsa_circ_173567,RMVar_hsa_circ_275838,RMVar_hsa_circ_122323,RMVar_hsa_circ_173571,RMVar_hsa_circ_23188,RMVar_hsa_circ_78515,RMVar_hsa_circ_173572,RMVar_hsa_circ_173573,RMVar_hsa_circ_173570 39206 RMVar_ID_39206 Human_SNP_ID_582589759 A-to-I Human chr15 - 71990499 71990499 71990499 CACCCGCCTCAGCCTCCCAAAGTGCTGGGATTATAGATGTGAGCCACTGCGCCCAGCCTAAATCT CACCCGCCTCAGCCTCCCAAAGTGCTGGGATTTTAGATGTGAGCCACTGCGCCCAGCCTAAATCT T A MYO9A Ensembl:ENSG00000066933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1206683016 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98023,RMVar_hsa_circ_50363,RMVar_hsa_circ_95039,RMVar_hsa_circ_173581,RMVar_hsa_circ_173580,RMVar_hsa_circ_2940,RMVar_hsa_circ_173590,RMVar_hsa_circ_78954,RMVar_hsa_circ_126402,RMVar_hsa_circ_173606,RMVar_hsa_circ_102510,RMVar_hsa_circ_173610,RMVar_hsa_circ_334579,RMVar_hsa_circ_34557,RMVar_hsa_circ_90032,RMVar_hsa_circ_340775,RMVar_hsa_circ_93421,RMVar_hsa_circ_173623,RMVar_hsa_circ_110089,RMVar_hsa_circ_30876,RMVar_hsa_circ_173624,RMVar_hsa_circ_173625,RMVar_hsa_circ_56369,RMVar_hsa_circ_49348,RMVar_hsa_circ_266026,RMVar_hsa_circ_315446,RMVar_hsa_circ_44508,RMVar_hsa_circ_173634,RMVar_hsa_circ_52787,RMVar_hsa_circ_330514,RMVar_hsa_circ_173628,RMVar_hsa_circ_173630,RMVar_hsa_circ_173631,RMVar_hsa_circ_173629,RMVar_hsa_circ_299996,RMVar_hsa_circ_304528,RMVar_hsa_circ_19736,RMVar_hsa_circ_31408,RMVar_hsa_circ_4401,RMVar_hsa_circ_173636,RMVar_hsa_circ_173637,RMVar_hsa_circ_173635,RMVar_hsa_circ_173643,RMVar_hsa_circ_173632,RMVar_hsa_circ_173633,RMVar_hsa_circ_335701,RMVar_hsa_circ_340397,RMVar_hsa_circ_290112,RMVar_hsa_circ_323579,RMVar_hsa_circ_173642,RMVar_hsa_circ_334439,RMVar_hsa_circ_336073,RMVar_hsa_circ_275086,RMVar_hsa_circ_281450,RMVar_hsa_circ_33923,RMVar_hsa_circ_173644,RMVar_hsa_circ_173646,RMVar_hsa_circ_173647,RMVar_hsa_circ_173645 39207 RMVar_ID_39207 Human_SNP_ID_582589760 A-to-I Human chr15 - 71990499 71990499 71990499 CACCCGCCTCAGCCTCCCAAAGTGCTGGGATTATAGATGTGAGCCACTGCGCCCAGCCTAAATCT CACCCGCCTCAGCCTCCCAAAGTGCTGGGATTGTAGATGTGAGCCACTGCGCCCAGCCTAAATCT T C MYO9A Ensembl:ENSG00000066933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1206683016 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98023,RMVar_hsa_circ_50363,RMVar_hsa_circ_95039,RMVar_hsa_circ_173581,RMVar_hsa_circ_173580,RMVar_hsa_circ_2940,RMVar_hsa_circ_173590,RMVar_hsa_circ_78954,RMVar_hsa_circ_126402,RMVar_hsa_circ_173606,RMVar_hsa_circ_102510,RMVar_hsa_circ_173610,RMVar_hsa_circ_334579,RMVar_hsa_circ_34557,RMVar_hsa_circ_90032,RMVar_hsa_circ_340775,RMVar_hsa_circ_93421,RMVar_hsa_circ_173623,RMVar_hsa_circ_110089,RMVar_hsa_circ_30876,RMVar_hsa_circ_173624,RMVar_hsa_circ_173625,RMVar_hsa_circ_56369,RMVar_hsa_circ_49348,RMVar_hsa_circ_266026,RMVar_hsa_circ_315446,RMVar_hsa_circ_44508,RMVar_hsa_circ_173634,RMVar_hsa_circ_52787,RMVar_hsa_circ_330514,RMVar_hsa_circ_173628,RMVar_hsa_circ_173630,RMVar_hsa_circ_173631,RMVar_hsa_circ_173629,RMVar_hsa_circ_299996,RMVar_hsa_circ_304528,RMVar_hsa_circ_19736,RMVar_hsa_circ_31408,RMVar_hsa_circ_4401,RMVar_hsa_circ_173636,RMVar_hsa_circ_173637,RMVar_hsa_circ_173635,RMVar_hsa_circ_173643,RMVar_hsa_circ_173632,RMVar_hsa_circ_173633,RMVar_hsa_circ_335701,RMVar_hsa_circ_340397,RMVar_hsa_circ_290112,RMVar_hsa_circ_323579,RMVar_hsa_circ_173642,RMVar_hsa_circ_334439,RMVar_hsa_circ_336073,RMVar_hsa_circ_275086,RMVar_hsa_circ_281450,RMVar_hsa_circ_33923,RMVar_hsa_circ_173644,RMVar_hsa_circ_173646,RMVar_hsa_circ_173647,RMVar_hsa_circ_173645 39208 RMVar_ID_39208 Human_SNP_ID_582601722 A-to-I Human chr15 - 72039580 72039580 72039580 ATGATCCACCCACCTCAGCCTCTTAAAGTGCTAGGATTACAGGCATGAGCCACTGTGCCTGGCCT ATGATCCACCCACCTCAGCCTCTTAAAGTGCTGGGATTACAGGCATGAGCCACTGTGCCTGGCCT T C MYO9A Ensembl:ENSG00000066933 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs879343788 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50363,RMVar_hsa_circ_340775,RMVar_hsa_circ_30876,RMVar_hsa_circ_44508,RMVar_hsa_circ_299996,RMVar_hsa_circ_173632,RMVar_hsa_circ_340397,RMVar_hsa_circ_323579,RMVar_hsa_circ_305682,RMVar_hsa_circ_173648,RMVar_hsa_circ_375638,RMVar_hsa_circ_173658,RMVar_hsa_circ_302163,RMVar_hsa_circ_173671,RMVar_hsa_circ_293561,RMVar_hsa_circ_173659,RMVar_hsa_circ_173667,RMVar_hsa_circ_173670,RMVar_hsa_circ_323073,RMVar_hsa_circ_311732,RMVar_hsa_circ_173674,RMVar_hsa_circ_173672,RMVar_hsa_circ_294261,RMVar_hsa_circ_173675,RMVar_hsa_circ_276004 39209 RMVar_ID_39209 Human_SNP_ID_582614579 A-to-I Human chr15 - 72091843 72091843 72091843 GGGCGTGGTGGCGGGCACCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGGAGAATGGTGTGA GGGCGTGGTGGCGGGCACCTGTAGTCCCAGCTGCTCGGGAGGCTGAGGCAGGGAGAATGGTGTGA T C MYO9A Ensembl:ENSG00000066933 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs868256645 Functional Loss SNV dbSNP153 33..33 33 - - - 39210 RMVar_ID_39210 Human_SNP_ID_582623603 A-to-I Human chr15 + 72125879 72125879 72125879 GGAGTCTCACTCTGTCGCCCAGGCTGTAGTGCAGTGGGGTGATCTCGGCTCACTGCAACCTCTGC GGAGTCTCACTCTGTCGCCCAGGCTGTAGTGCGGTGGGGTGATCTCGGCTCACTGCAACCTCTGC A G SENP8 Ensembl:ENSG00000166192 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1447501176 Functional Loss SNV dbSNP153 33..33 33 - - - 39211 RMVar_ID_39211 Human_SNP_ID_582625480 A-to-I Human chr15 + 72134458 72134458 72134458 AAAATTAGCCAGGCATGGTGGTACGCACCTGCAGTCCTAGCTACTCTGGAGGCAGAAGCCAGAAA AAAATTAGCCAGGCATGGTGGTACGCACCTGCGGTCCTAGCTACTCTGGAGGCAGAAGCCAGAAA A G SENP8 Ensembl:ENSG00000166192 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs960082177 Functional Loss SNV dbSNP153 33..33 33 - - - 39212 RMVar_ID_39212 Human_SNP_ID_582640533 A-to-I Human chr15 - 72199192 72199192 72199192 CGACTCTGGCCCTGGCCCTTACTTGCTTCTCTAGCTCTCTAGGCCTCTCCAGTTTGCACCTGTCC CGACTCTGGCCCTGGCCCTTACTTGCTTCTCTCGCTCTCTAGGCCTCTCCAGTTTGCACCTGTCC T G PKM Ensembl:ENSG00000067225 Protein coding exon GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs987675460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_462803,Human_RBP_ID_1001885,Human_RBP_ID_1175605,Human_RBP_ID_1279474,Human_RBP_ID_1507819,Human_RBP_ID_1833404,Human_RBP_ID_2453237,Human_RBP_ID_3481636,Human_RBP_ID_4331814,Human_RBP_ID_6458237,Human_RBP_ID_8421857,Human_RBP_ID_9055932,Human_RBP_ID_12576866,Human_RBP_ID_17250954,Human_RBP_ID_17366199,Human_RBP_ID_17483600,Human_RBP_ID_17652339,Human_RBP_ID_17865863,Human_RBP_ID_18281861,Human_RBP_ID_18436755,Human_RBP_ID_18667360,Human_RBP_ID_18938295,Human_RBP_ID_20004206,Human_RBP_ID_22193189,Human_RBP_ID_23162252,Human_RBP_ID_23209133,Human_RBP_ID_23664619,Human_RBP_ID_24412002,Human_RBP_ID_24474483,Human_RBP_ID_26435709,Human_RBP_ID_26934013,Human_RBP_ID_27155636,Human_RBP_ID_27233670,Human_RBP_ID_27436658 Human_miRNA_ID_1261510,Human_miRNA_ID_1339178 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 39213 RMVar_ID_39213 Human_SNP_ID_582643146 A-to-I Human chr15 - 72208840 72208840 72208840 GGAGGTGGAAAATGGTGGCTCCTTGGGCAGCAAGAAGGGTGTGAACCTTCCTGGGGCTGCTGTGG GGAGGTGGAAAATGGTGGCTCCTTGGGCAGCAGGAAGGGTGTGAACCTTCCTGGGGCTGCTGTGG T C PKM Ensembl:ENSG00000067225 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1158061359 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_887147,Human_RBP_ID_1507880,Human_RBP_ID_1833450,Human_RBP_ID_3945662,Human_RBP_ID_4331873,Human_RBP_ID_6458352,Human_RBP_ID_8421919,Human_RBP_ID_8804115,Human_RBP_ID_9055944,Human_RBP_ID_17870493,Human_RBP_ID_18982374,Human_RBP_ID_22439856,Human_RBP_ID_22532606,Human_RBP_ID_22759286,Human_RBP_ID_22799190,Human_RBP_ID_26934082,Human_RBP_ID_27155666,Human_RBP_ID_27233710,Human_RBP_ID_27810496 Human_Splice_Rec_1621770,Human_Splice_Rec_1621786,Human_Splice_Rec_1621800,Human_Splice_Rec_1621814,Human_Splice_Rec_1621830,Human_Splice_Rec_1621856,Human_Splice_Rec_1621874,Human_Splice_Rec_1621890,Human_Splice_Rec_1621906,Human_Splice_Rec_1621922,Human_Splice_Rec_1621930 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 39214 RMVar_ID_39214 Human_SNP_ID_582644199 A-to-I Human chr15 - 72212258 72212258 72212258 GTTGGCCTGGTTGTTGTCAATCTCTTGATCTCATGATCCACCCGCCTTGGCCTTCCAAAGTGTTT GTTGGCCTGGTTGTTGTCAATCTCTTGATCTCGTGATCCACCCGCCTTGGCCTTCCAAAGTGTTT T C PKM Ensembl:ENSG00000067225 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs12437619 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12577140 GWAS_ID_4647,GWAS_ID_4648,GWAS_ID_4649,GWAS_ID_4650,GWAS_ID_4651,GWAS_ID_4652,GWAS_ID_4653,GWAS_ID_4654,GWAS_ID_4655,GWAS_ID_4656,GWAS_ID_4657,GWAS_ID_4658,GWAS_ID_4659,GWAS_ID_4660,GWAS_ID_4661,GWAS_ID_4662,GWAS_ID_4663,GWAS_ID_4664,GWAS_ID_4665,GWAS_ID_4666,GWAS_ID_4667,GWAS_ID_4668,GWAS_ID_4669,GWAS_ID_4670,GWAS_ID_4671,GWAS_ID_4672,GWAS_ID_4673,GWAS_ID_4674,GWAS_ID_4675,GWAS_ID_4676,GWAS_ID_4677 RMVar_hsa_circ_121437,RMVar_hsa_circ_125401,RMVar_hsa_circ_123724,RMVar_hsa_circ_103902,RMVar_hsa_circ_173681,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_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_291740,RMVar_hsa_circ_95622,RMVar_hsa_circ_173701 39215 RMVar_ID_39215 Human_SNP_ID_582644200 A-to-I Human chr15 - 72212258 72212258 72212259 GTTGGCCTGGTTGTTGTCAATCTCTTGATCTCATGATCCACCCGCCTTGGCCTTCCAAAGTGTTT GTTGGCCTGGTTGTTGTCAATCTCTTGATCTTGTGATCCACCCGCCTTGGCCTTCCAAAGTGTTT TG CA PKM Ensembl:ENSG00000067225 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs386785263 Functional Loss MNV dbSNP153 32..33 33 - - - Human_RBP_ID_12577140 RMVar_hsa_circ_121437,RMVar_hsa_circ_125401,RMVar_hsa_circ_123724,RMVar_hsa_circ_103902,RMVar_hsa_circ_173681,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_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_291740,RMVar_hsa_circ_95622,RMVar_hsa_circ_173701 39216 RMVar_ID_39216 Human_SNP_ID_582644216 A-to-I Human chr15 - 72212313 72212308 72212313 ACGCCACCACGCCCAGCTAATTTTTGTATTTTAAGTTGAGACGAGGTTTCACCATGTTGGCCTGG ACGCCACCACGCCCAGCTAATTTTTGTATTTT_____GAGACGAGGTTTCACCATGTTGGCCTGG CAACTT C PKM Ensembl:ENSG00000067225 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1263861901 Functional Loss DEL dbSNP153 33..37 33 - - - Human_RBP_ID_12577144 RMVar_hsa_circ_121437,RMVar_hsa_circ_125401,RMVar_hsa_circ_123724,RMVar_hsa_circ_103902,RMVar_hsa_circ_173681,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_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_291740,RMVar_hsa_circ_95622,RMVar_hsa_circ_173701 39217 RMVar_ID_39217 Human_SNP_ID_582644217 A-to-I Human chr15 - 72212318 72212318 72212318 GGTGCACGCCACCACGCCCAGCTAATTTTTGTATTTTAAGTTGAGACGAGGTTTCACCATGTTGG GGTGCACGCCACCACGCCCAGCTAATTTTTGTGTTTTAAGTTGAGACGAGGTTTCACCATGTTGG T C PKM Ensembl:ENSG00000067225 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs952282961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12577145 RMVar_hsa_circ_121437,RMVar_hsa_circ_125401,RMVar_hsa_circ_123724,RMVar_hsa_circ_103902,RMVar_hsa_circ_173681,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_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_291740,RMVar_hsa_circ_95622,RMVar_hsa_circ_173701 39218 RMVar_ID_39218 Human_SNP_ID_582644230 A-to-I Human chr15 - 72212375 72212375 72212375 TGCCTCCTAGGTTCAAGTGGTTCTCTTGCCTCAGCCTCCTGAATAGCTGGGACTACAGGTGCACG TGCCTCCTAGGTTCAAGTGGTTCTCTTGCCTCGGCCTCCTGAATAGCTGGGACTACAGGTGCACG T C PKM Ensembl:ENSG00000067225 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs924731175 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121437,RMVar_hsa_circ_125401,RMVar_hsa_circ_123724,RMVar_hsa_circ_103902,RMVar_hsa_circ_173681,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_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_291740,RMVar_hsa_circ_95622,RMVar_hsa_circ_173701 39219 RMVar_ID_39219 Human_SNP_ID_582644510 A-to-I Human chr15 - 72213559 72213559 72213559 GGGCATGGTGGCACATGCCTGCAGTCCCAGCTACTCGGGAGCCTGAGGCAGGAGAATCGCTTGAA GGGCATGGTGGCACATGCCTGCAGTCCCAGCTGCTCGGGAGCCTGAGGCAGGAGAATCGCTTGAA T C PKM Ensembl:ENSG00000067225 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1351117583 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121437,RMVar_hsa_circ_125401,RMVar_hsa_circ_123724,RMVar_hsa_circ_103902,RMVar_hsa_circ_173681,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_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_291740,RMVar_hsa_circ_95622,RMVar_hsa_circ_173701 39220 RMVar_ID_39220 Human_SNP_ID_582644896 A-to-I Human chr15 - 72215115 72215115 72215115 CTCACCACAACCTCTGCCTCCCAGGTTCAAGCAATTCTCATACCTCAGCCTCCTGAGTAGCTGGG CTCACCACAACCTCTGCCTCCCAGGTTCAAGCGATTCTCATACCTCAGCCTCCTGAGTAGCTGGG T C PKM Ensembl:ENSG00000067225 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6494993 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121437,RMVar_hsa_circ_125401,RMVar_hsa_circ_123724,RMVar_hsa_circ_103902,RMVar_hsa_circ_173681,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_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_291740,RMVar_hsa_circ_95622,RMVar_hsa_circ_173701 39221 RMVar_ID_39221 Human_SNP_ID_582647107 A-to-I Human chr15 - 72224678 72224678 72224678 TTGTATGTTTAGTAGTGATGGTGTTTCACCATATTAGCCAGGCTGGTCTCGAACTCTTAGCCTCA TTGTATGTTTAGTAGTGATGGTGTTTCACCATGTTAGCCAGGCTGGTCTCGAACTCTTAGCCTCA T C PKM Ensembl:ENSG00000067225 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1187637539 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17688972 RMVar_hsa_circ_125401,RMVar_hsa_circ_173678,RMVar_hsa_circ_122708,RMVar_hsa_circ_173694,RMVar_hsa_circ_127337,RMVar_hsa_circ_173703,RMVar_hsa_circ_89744,RMVar_hsa_circ_173704 39222 RMVar_ID_39222 Human_SNP_ID_582647108 A-to-I Human chr15 - 72224680 72224680 72224680 TTTTGTATGTTTAGTAGTGATGGTGTTTCACCATATTAGCCAGGCTGGTCTCGAACTCTTAGCCT TTTTGTATGTTTAGTAGTGATGGTGTTTCACCGTATTAGCCAGGCTGGTCTCGAACTCTTAGCCT T C PKM Ensembl:ENSG00000067225 Protein coding intron GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs773017961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17688972 RMVar_hsa_circ_125401,RMVar_hsa_circ_173678,RMVar_hsa_circ_122708,RMVar_hsa_circ_173694,RMVar_hsa_circ_127337,RMVar_hsa_circ_173703,RMVar_hsa_circ_89744,RMVar_hsa_circ_173704 39223 RMVar_ID_39223 Human_SNP_ID_582647113 A-to-I Human chr15 - 72224697 72224697 72224697 GTGCGCGCCTGGCTAATTTTTGTATGTTTAGTAGTGATGGTGTTTCACCATATTAGCCAGGCTGG GTGCGCGCCTGGCTAATTTTTGTATGTTTAGTGGTGATGGTGTTTCACCATATTAGCCAGGCTGG T C PKM Ensembl:ENSG00000067225 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1250974666 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125401,RMVar_hsa_circ_173678,RMVar_hsa_circ_122708,RMVar_hsa_circ_173694,RMVar_hsa_circ_127337,RMVar_hsa_circ_173703,RMVar_hsa_circ_89744,RMVar_hsa_circ_173704 39224 RMVar_ID_39224 Human_SNP_ID_582647126 A-to-I Human chr15 - 72224746 72224746 72224746 GGATTCAAGCAATTCTGTGTCTCAGCCACCCAAGTAGCTGGGATTACAGGTGCGCGCCTGGCTAA GGATTCAAGCAATTCTGTGTCTCAGCCACCCAGGTAGCTGGGATTACAGGTGCGCGCCTGGCTAA T C PKM Ensembl:ENSG00000067225 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1169586981 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6458472,Human_RBP_ID_17563280 RMVar_hsa_circ_125401,RMVar_hsa_circ_173678,RMVar_hsa_circ_122708,RMVar_hsa_circ_173694,RMVar_hsa_circ_127337,RMVar_hsa_circ_173703,RMVar_hsa_circ_89744,RMVar_hsa_circ_173704 39225 RMVar_ID_39225 Human_SNP_ID_582652317 A-to-I Human chr15 - 72245251 72245251 72245251 TCACGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCCACCACCACGCCCA TCACGCCATTCTCCTGCCTCAGCCTCCCGAGTGGCTGGGACTACAGGCGCCCACCACCACGCCCA T C PARP6 Ensembl:ENSG00000137817 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs953821925 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_31452,RMVar_hsa_circ_85467,RMVar_hsa_circ_339985,RMVar_hsa_circ_173710,RMVar_hsa_circ_50431,RMVar_hsa_circ_112698,RMVar_hsa_circ_173711,RMVar_hsa_circ_44479 39226 RMVar_ID_39226 Human_SNP_ID_582652332 A-to-I Human chr15 - 72245300 72245300 72245300 GGAGTGCAGTGGCGCGGTCTCAGCTCACTGCAAGCTCTACCTCCCGGGTTCACGCCATTCTCCTG GGAGTGCAGTGGCGCGGTCTCAGCTCACTGCAGGCTCTACCTCCCGGGTTCACGCCATTCTCCTG T C PARP6 Ensembl:ENSG00000137817 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1202146282 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_31452,RMVar_hsa_circ_85467,RMVar_hsa_circ_339985,RMVar_hsa_circ_173710,RMVar_hsa_circ_50431,RMVar_hsa_circ_112698,RMVar_hsa_circ_173711,RMVar_hsa_circ_44479 39227 RMVar_ID_39227 Human_SNP_ID_582652346 A-to-I Human chr15 - 72245344 72245344 72245344 TTGTTTTGTTTTTTGAGACAGAGTCTCACTCTATCGCCCAGGCTGGAGTGCAGTGGCGCGGTCTC TTGTTTTGTTTTTTGAGACAGAGTCTCACTCTTTCGCCCAGGCTGGAGTGCAGTGGCGCGGTCTC T A PARP6 Ensembl:ENSG00000137817 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs560097716 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_31452,RMVar_hsa_circ_85467,RMVar_hsa_circ_339985,RMVar_hsa_circ_173710,RMVar_hsa_circ_50431,RMVar_hsa_circ_112698,RMVar_hsa_circ_173711,RMVar_hsa_circ_44479 39228 RMVar_ID_39228 Human_SNP_ID_582652347 A-to-I Human chr15 - 72245344 72245344 72245344 TTGTTTTGTTTTTTGAGACAGAGTCTCACTCTATCGCCCAGGCTGGAGTGCAGTGGCGCGGTCTC TTGTTTTGTTTTTTGAGACAGAGTCTCACTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCGGTCTC T C PARP6 Ensembl:ENSG00000137817 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs560097716 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_31452,RMVar_hsa_circ_85467,RMVar_hsa_circ_339985,RMVar_hsa_circ_173710,RMVar_hsa_circ_50431,RMVar_hsa_circ_112698,RMVar_hsa_circ_173711,RMVar_hsa_circ_44479 39229 RMVar_ID_39229 Human_SNP_ID_582652348 A-to-I Human chr15 - 72245349 72245345 72245349 TTGTTTTGTTTTGTTTTTTGAGACAGAGTCTCACTCTATCGCCCAGGCTGGAGTGCAGTGGCGCG TTGTTTTGTTTTGTTTTTTGAGACAGAGTCTC____TATCGCCCAGGCTGGAGTGCAGTGGCGCG AGAGT A PARP6 Ensembl:ENSG00000137817 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1471959096 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_31452,RMVar_hsa_circ_85467,RMVar_hsa_circ_339985,RMVar_hsa_circ_173710,RMVar_hsa_circ_50431,RMVar_hsa_circ_112698,RMVar_hsa_circ_173711,RMVar_hsa_circ_44479 39230 RMVar_ID_39230 Human_SNP_ID_582655972 A-to-I Human chr15 - 72260640 72260640 72260640 ATCATACAGGACTCCATGCTGAAAGGCAAACTAGGTGTACCAGAGCTTCGGGTTGGGCGCCTCAT ATCATACAGGACTCCATGCTGAAAGGCAAACTGGGTGTACCAGAGCTTCGGGTTGGGCGCCTCAT T C PARP6 Ensembl:ENSG00000137817 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs753863683 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_462902,Human_RBP_ID_3945677,Human_RBP_ID_17252312,Human_RBP_ID_17366218,Human_RBP_ID_25183774 Human_Splice_Rec_1621994,Human_Splice_Rec_1622036,Human_Splice_Rec_1622076,Human_Splice_Rec_1622114,Human_Splice_Rec_1622152,Human_Splice_Rec_1622198,Human_Splice_Rec_1622232,Human_Splice_Rec_1622270,Human_Splice_Rec_1622314,Human_Splice_Rec_1622362,Human_Splice_Rec_1622424,Human_Splice_Rec_1622484 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_350319,RMVar_hsa_circ_7425 39231 RMVar_ID_39231 Human_SNP_ID_582672254 A-to-I Human chr15 - 72330423 72330423 72330423 GGAGTCACTACCTCTGTTGCCCAGGCTGGAGTACAGTGGCACGATCTCGGTTCACTGAACCTCTG GGAGTCACTACCTCTGTTGCCCAGGCTGGAGTGCAGTGGCACGATCTCGGTTCACTGAACCTCTG T C AC009690.1 Ensembl:ENSG00000260729 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1224170990 Functional Loss SNV dbSNP153 33..33 33 - - - 39232 RMVar_ID_39232 Human_SNP_ID_582672509 A-to-I Human chr15 - 72331551 72331551 72331551 GGAGGCTGAGGTGGGAGGATCACTTGAGTCCCAGGCAGTCAAGGCTGCAGTGAGCTATTGTGATG GGAGGCTGAGGTGGGAGGATCACTTGAGTCCCCGGCAGTCAAGGCTGCAGTGAGCTATTGTGATG T G AC009690.1 Ensembl:ENSG00000260729 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1222515405 Functional Loss SNV dbSNP153 33..33 33 - - - 39233 RMVar_ID_39233 Human_SNP_ID_582672591 A-to-I Human chr15 - 72331847 72331847 72331847 TTTTATTATTATTATTTTTTTTTTGGAGATAGAGTCTCACTCTGTCGCCCAGGCTGGAGTGCAGT TTTTATTATTATTATTTTTTTTTTGGAGATAGGGTCTCACTCTGTCGCCCAGGCTGGAGTGCAGT T C AC009690.1 Ensembl:ENSG00000260729 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs566186079 Functional Loss SNV dbSNP153 33..33 33 - - - 39234 RMVar_ID_39234 Human_SNP_ID_582672592 A-to-I Human chr15 - 72331849 72331849 72331849 TCTTTTATTATTATTATTTTTTTTTTGGAGATAGAGTCTCACTCTGTCGCCCAGGCTGGAGTGCA TCTTTTATTATTATTATTTTTTTTTTGGAGATGGAGTCTCACTCTGTCGCCCAGGCTGGAGTGCA T C AC009690.1 Ensembl:ENSG00000260729 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs897383414 Functional Loss SNV dbSNP153 33..33 33 - - - 39235 RMVar_ID_39235 Human_SNP_ID_582674301 A-to-I Human chr15 - 72338514 72338514 72338514 GAGCTCCTGAACTCAGGTGATCCACACACCTCAGCCTCCCAAAGTGCTGGGATTACAAGCATGAG GAGCTCCTGAACTCAGGTGATCCACACACCTCGGCCTCCCAAAGTGCTGGGATTACAAGCATGAG T C AC009690.1 Ensembl:ENSG00000260729 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1443659644 Functional Loss SNV dbSNP153 33..33 33 - - - 39236 RMVar_ID_39236 Human_SNP_ID_582675516 A-to-I Human chr15 - 72343348 72343348 72343348 TCTGTCGCCCAGGCTGACAGTGCAGTGGCACAATCTTGGCTCACTGCAGCCTCTGCCTCCTGGGT TCTGTCGCCCAGGCTGACAGTGCAGTGGCACAGTCTTGGCTCACTGCAGCCTCTGCCTCCTGGGT T C HEXA,AC009690.1 Ensembl:ENSG00000213614,Ensembl:ENSG00000260729 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027365460 Functional Loss SNV dbSNP153 33..33 33 - - - 39237 RMVar_ID_39237 Human_SNP_ID_582677948 A-to-I Human chr15 - 72352445 72352445 72352445 ACAGCGTCTCAATTTTTTTTTTTTTTTTTTGTATTTTTTGTAGAGCTGGGGTTTCGTCATGTTAC ACAGCGTCTCAATTTTTTTTTTTTTTTTTTGTTTTTTTTGTAGAGCTGGGGTTTCGTCATGTTAC T A HEXA,AC009690.1 Ensembl:ENSG00000213614,Ensembl:ENSG00000260729 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1024717663 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20561,RMVar_hsa_circ_53682,RMVar_hsa_circ_279793,RMVar_hsa_circ_173724,RMVar_hsa_circ_369029,RMVar_hsa_circ_122311,RMVar_hsa_circ_54327,RMVar_hsa_circ_112268,RMVar_hsa_circ_173726,RMVar_hsa_circ_8508,RMVar_hsa_circ_311213,RMVar_hsa_circ_333107,RMVar_hsa_circ_173727,RMVar_hsa_circ_62198,RMVar_hsa_circ_364595,RMVar_hsa_circ_289926,RMVar_hsa_circ_173728,RMVar_hsa_circ_369428,RMVar_hsa_circ_173729 39238 RMVar_ID_39238 Human_SNP_ID_582678959 A-to-I Human chr15 - 72356546 72356546 72356546 CTGTAGTCACACCTGGATGTAACCAGCTTCCTACTTTGGAGTCAGTGGAGAATTGTAAGTACCAT CTGTAGTCACACCTGGATGTAACCAGCTTCCTTCTTTGGAGTCAGTGGAGAATTGTAAGTACCAT T A HEXA,AC009690.1 Ensembl:ENSG00000213614,Ensembl:ENSG00000260729 Protein coding,Protein coding CDS,CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1269110075 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_884367,Human_RBP_ID_1364063,Human_RBP_ID_1833561,Human_RBP_ID_2453365,Human_RBP_ID_3946545,Human_RBP_ID_17865933,Human_RBP_ID_18667572,Human_RBP_ID_18981633,Human_RBP_ID_19068508,Human_RBP_ID_22758896 Human_Splice_Rec_1622648,Human_Splice_Rec_1622649,Human_Splice_Rec_1622678,Human_Splice_Rec_1622679,Human_Splice_Rec_1622710,Human_Splice_Rec_1622711,Human_Splice_Rec_1622735,Human_Splice_Rec_1622762,Human_Splice_Rec_1622763,Human_Splice_Rec_1622781,Human_Splice_Rec_1622800,Human_Splice_Rec_1622801,Human_Splice_Rec_1622826,Human_Splice_Rec_1622827,Human_Splice_Rec_1622838,Human_Splice_Rec_1622839,Human_Splice_Rec_1622856,Human_Splice_Rec_1622857,Human_Splice_Rec_1622878,Human_Splice_Rec_1622879,Human_Splice_Rec_1622886,Human_Splice_Rec_1622887,Human_Splice_Rec_1622896,Human_Splice_Rec_1622897 RMVar_hsa_circ_173732,RMVar_hsa_circ_20561,RMVar_hsa_circ_279793,RMVar_hsa_circ_173724,RMVar_hsa_circ_122311,RMVar_hsa_circ_8508,RMVar_hsa_circ_173727,RMVar_hsa_circ_62198,RMVar_hsa_circ_289926,RMVar_hsa_circ_173730,RMVar_hsa_circ_173728,RMVar_hsa_circ_362805,RMVar_hsa_circ_112924,RMVar_hsa_circ_173731,RMVar_hsa_circ_364480,RMVar_hsa_circ_269604,RMVar_hsa_circ_327554,RMVar_hsa_circ_117457,RMVar_hsa_circ_173733 39239 RMVar_ID_39239 Human_SNP_ID_582681344 A-to-I Human chr15 - 72367040 72367040 72367040 ACTCTGGAGGCTGAGGCAGCAGAATCGCTTGAATCCAGGAGGTGGAGGTTGCAGTGAGCCGAGAG ACTCTGGAGGCTGAGGCAGCAGAATCGCTTGAGTCCAGGAGGTGGAGGTTGCAGTGAGCCGAGAG T C HEXA,AC009690.1 Ensembl:ENSG00000213614,Ensembl:ENSG00000260729 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1567304843 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122311,RMVar_hsa_circ_173727,RMVar_hsa_circ_117457,RMVar_hsa_circ_173733 39240 RMVar_ID_39240 Human_SNP_ID_582682714 A-to-I Human chr15 - 72372950 72372950 72372950 ATTTTTGTATTTTCTGTAGATGGGGTTTCGCCATGTTGCCCAAGCTGGTCTCCAATTCCTGAGCT ATTTTTGTATTTTCTGTAGATGGGGTTTCGCCGTGTTGCCCAAGCTGGTCTCCAATTCCTGAGCT T C HEXA,AC009690.1 Ensembl:ENSG00000213614,Ensembl:ENSG00000260729 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs772676240 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6458879,Human_RBP_ID_12579304 RMVar_hsa_circ_122311,RMVar_hsa_circ_173727,RMVar_hsa_circ_117457,RMVar_hsa_circ_173733 39241 RMVar_ID_39241 Human_SNP_ID_582706118 A-to-I Human chr15 - 72466717 72466717 72466717 AGTATGGTCTTGATCTCCTGACCTCGTGATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTAC AGTATGGTCTTGATCTCCTGACCTCGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTAC T C TMEM202-AS1 Ensembl:ENSG00000261423 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1009502342 Functional Loss SNV dbSNP153 33..33 33 - - - 39242 RMVar_ID_39242 Human_SNP_ID_582706565 A-to-I Human chr15 - 72468496 72468496 72468496 GTGACTCATGCCTGTAATCCCAGCACTTTGGAAGACCAAGGTGGGACAATTACGTGAGGCTAGGA GTGACTCATGCCTGTAATCCCAGCACTTTGGAGGACCAAGGTGGGACAATTACGTGAGGCTAGGA T C TMEM202-AS1 Ensembl:ENSG00000261423 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1419250401 Functional Loss SNV dbSNP153 33..33 33 - - - 39243 RMVar_ID_39243 Human_SNP_ID_582707400 A-to-I Human chr15 - 72471986 72471986 72471986 TTGCTCAGACTGGTCTGGAACTCCTGGCCTCAAGCAATCCTCCCACCTTGGCCTCCCAAAATGCT TTGCTCAGACTGGTCTGGAACTCCTGGCCTCACGCAATCCTCCCACCTTGGCCTCCCAAAATGCT T G TMEM202-AS1 Ensembl:ENSG00000261423 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs919324535 Functional Loss SNV dbSNP153 33..33 33 - - - 39244 RMVar_ID_39244 Human_SNP_ID_582707404 A-to-I Human chr15 - 72472021 72472021 72472021 TTTTTTATTTTTTTTTACAGATACATCTCACTATGTTGCTCAGACTGGTCTGGAACTCCTGGCCT TTTTTTATTTTTTTTTACAGATACATCTCACTGTGTTGCTCAGACTGGTCTGGAACTCCTGGCCT T C TMEM202-AS1 Ensembl:ENSG00000261423 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1255929750 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6458936 39245 RMVar_ID_39245 Human_SNP_ID_582709125 A-to-I Human chr15 + 72477899 72477899 72477899 GTGATCTCAGCTTACTGCAACCTCTCCCTCCCAGGTTCAAGAGATTCCCCTTGCCTCAGCTTCCC GTGATCTCAGCTTACTGCAACCTCTCCCTCCCGGGTTCAAGAGATTCCCCTTGCCTCAGCTTCCC A G ARIH1 Ensembl:ENSG00000166233 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs901110508 Functional Loss SNV dbSNP153 33..33 33 - - - 39246 RMVar_ID_39246 Human_SNP_ID_582712413 A-to-I Human chr15 + 72490113 72490113 72490113 GGCCAGTCACGGTGGTTCAAGCGTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGAGGATTGAT GGCCAGTCACGGTGGTTCAAGCGTGTAATCCCGGCACTTTGGGAGGCTGAGGCAGGAGGATTGAT A G ARIH1 Ensembl:ENSG00000166233 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1189783778 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12580023 39247 RMVar_ID_39247 Human_SNP_ID_582712415 A-to-I Human chr15 + 72490124 72490124 72490124 GTGGTTCAAGCGTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGAGGATTGATAGAACCAAGGA GTGGTTCAAGCGTGTAATCCCAGCACTTTGGGGGGCTGAGGCAGGAGGATTGATAGAACCAAGGA A G ARIH1 Ensembl:ENSG00000166233 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1444525040 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6459130,Human_RBP_ID_12580023 39248 RMVar_ID_39248 Human_SNP_ID_582716705 A-to-I Human chr15 + 72507298 72507298 72507298 CGCCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCATGCCTGGCTTTGGTTG CGCCTGCCTTGGCCTCCCAAAGTGCTGGGATTGCAGGCGTGAGCCACCATGCCTGGCTTTGGTTG A G ARIH1 Ensembl:ENSG00000166233 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965510060 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_173737,RMVar_hsa_circ_173739,RMVar_hsa_circ_82587,RMVar_hsa_circ_310357,RMVar_hsa_circ_173738,RMVar_hsa_circ_173736 39249 RMVar_ID_39249 Human_SNP_ID_582716772 A-to-I Human chr15 + 72507578 72507578 72507578 CTAGATGGCTGTGCACAGTGGCTCATTCCTATAATCCCTGTGTTTTGGGAGGCTGAAGCTGGAGG CTAGATGGCTGTGCACAGTGGCTCATTCCTATGATCCCTGTGTTTTGGGAGGCTGAAGCTGGAGG A G ARIH1 Ensembl:ENSG00000166233 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs557977220 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_173737,RMVar_hsa_circ_173739,RMVar_hsa_circ_82587,RMVar_hsa_circ_310357,RMVar_hsa_circ_173738,RMVar_hsa_circ_173736 39250 RMVar_ID_39250 Human_SNP_ID_582718410 A-to-I Human chr15 + 72513986 72513986 72513986 CAACCTCAGCCTCCTCAGCTACTGGGACTAATACGCCACCACGCCCAGCTAATTTTTTGTAGTTT CAACCTCAGCCTCCTCAGCTACTGGGACTAATTCGCCACCACGCCCAGCTAATTTTTTGTAGTTT A T ARIH1 Ensembl:ENSG00000166233 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1375664503 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_173737,RMVar_hsa_circ_173739,RMVar_hsa_circ_82587,RMVar_hsa_circ_310357,RMVar_hsa_circ_173738,RMVar_hsa_circ_173736 39251 RMVar_ID_39251 Human_SNP_ID_582721506 A-to-I Human chr15 + 72525869 72525869 72525869 TGCTATGTTGTCCAGGCTGGTCTCAAACTCCTAGACACAAGCGATCCTCTCACCTCAGCCCCACA TGCTATGTTGTCCAGGCTGGTCTCAAACTCCTCGACACAAGCGATCCTCTCACCTCAGCCCCACA A C ARIH1 Ensembl:ENSG00000166233 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1324161489 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_173741,RMVar_hsa_circ_22124,RMVar_hsa_circ_173737,RMVar_hsa_circ_82587,RMVar_hsa_circ_173738,RMVar_hsa_circ_289375,RMVar_hsa_circ_307863,RMVar_hsa_circ_173736,RMVar_hsa_circ_309093,RMVar_hsa_circ_294931,RMVar_hsa_circ_279703,RMVar_hsa_circ_281490,RMVar_hsa_circ_270334,RMVar_hsa_circ_173743,RMVar_hsa_circ_173745,RMVar_hsa_circ_173746,RMVar_hsa_circ_173747,RMVar_hsa_circ_173744,RMVar_hsa_circ_173742 39252 RMVar_ID_39252 Human_SNP_ID_582721507 A-to-I Human chr15 + 72525869 72525869 72525869 TGCTATGTTGTCCAGGCTGGTCTCAAACTCCTAGACACAAGCGATCCTCTCACCTCAGCCCCACA TGCTATGTTGTCCAGGCTGGTCTCAAACTCCTGGACACAAGCGATCCTCTCACCTCAGCCCCACA A G ARIH1 Ensembl:ENSG00000166233 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1324161489 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_173741,RMVar_hsa_circ_22124,RMVar_hsa_circ_173737,RMVar_hsa_circ_82587,RMVar_hsa_circ_173738,RMVar_hsa_circ_289375,RMVar_hsa_circ_307863,RMVar_hsa_circ_173736,RMVar_hsa_circ_309093,RMVar_hsa_circ_294931,RMVar_hsa_circ_279703,RMVar_hsa_circ_281490,RMVar_hsa_circ_270334,RMVar_hsa_circ_173743,RMVar_hsa_circ_173745,RMVar_hsa_circ_173746,RMVar_hsa_circ_173747,RMVar_hsa_circ_173744,RMVar_hsa_circ_173742 39253 RMVar_ID_39253 Human_SNP_ID_582722125 A-to-I Human chr15 + 72528561 72528561 72528561 TATTCTACAATACAGTGAAATTTTTCCTGTTTAAACAATCCACGGCCGGGCACAGTGGCTCATGC TATTCTACAATACAGTGAAATTTTTCCTGTTTGAACAATCCACGGCCGGGCACAGTGGCTCATGC A G ARIH1 Ensembl:ENSG00000166233 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1364349507 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25163060 RMVar_hsa_circ_173741,RMVar_hsa_circ_22124,RMVar_hsa_circ_173737,RMVar_hsa_circ_82587,RMVar_hsa_circ_173738,RMVar_hsa_circ_289375,RMVar_hsa_circ_307863,RMVar_hsa_circ_173736,RMVar_hsa_circ_309093,RMVar_hsa_circ_294931,RMVar_hsa_circ_279703,RMVar_hsa_circ_281490,RMVar_hsa_circ_270334,RMVar_hsa_circ_173743,RMVar_hsa_circ_173745,RMVar_hsa_circ_173746,RMVar_hsa_circ_173747,RMVar_hsa_circ_173744,RMVar_hsa_circ_173742 39254 RMVar_ID_39254 Human_SNP_ID_582722146 A-to-I Human chr15 + 72528628 72528628 72528628 GTGATCCCAGAACTTTAGCTGACTGTGGCAGGAAGATCGCTTGAGCGTAGGAGTTTGAGACTAGC GTGATCCCAGAACTTTAGCTGACTGTGGCAGGGAGATCGCTTGAGCGTAGGAGTTTGAGACTAGC A G ARIH1 Ensembl:ENSG00000166233 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1354539771 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6459524,Human_RBP_ID_12581037,Human_RBP_ID_23665071 RMVar_hsa_circ_173741,RMVar_hsa_circ_22124,RMVar_hsa_circ_173737,RMVar_hsa_circ_82587,RMVar_hsa_circ_173738,RMVar_hsa_circ_289375,RMVar_hsa_circ_307863,RMVar_hsa_circ_173736,RMVar_hsa_circ_309093,RMVar_hsa_circ_294931,RMVar_hsa_circ_279703,RMVar_hsa_circ_281490,RMVar_hsa_circ_270334,RMVar_hsa_circ_173743,RMVar_hsa_circ_173745,RMVar_hsa_circ_173746,RMVar_hsa_circ_173747,RMVar_hsa_circ_173744,RMVar_hsa_circ_173742 39255 RMVar_ID_39255 Human_SNP_ID_582722377 A-to-I Human chr15 + 72529370 72529370 72529370 GCTCAAACTGATTCTCTCGCCTCAGCCTCCCTAGTGGGTAGGACTGTGCACCACAACACCTAGCA GCTCAAACTGATTCTCTCGCCTCAGCCTCCCTCGTGGGTAGGACTGTGCACCACAACACCTAGCA A C ARIH1 Ensembl:ENSG00000166233 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054551671 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_173741,RMVar_hsa_circ_22124,RMVar_hsa_circ_173737,RMVar_hsa_circ_82587,RMVar_hsa_circ_173738,RMVar_hsa_circ_289375,RMVar_hsa_circ_307863,RMVar_hsa_circ_173736,RMVar_hsa_circ_309093,RMVar_hsa_circ_294931,RMVar_hsa_circ_279703,RMVar_hsa_circ_281490,RMVar_hsa_circ_270334,RMVar_hsa_circ_173743,RMVar_hsa_circ_173745,RMVar_hsa_circ_173746,RMVar_hsa_circ_173747,RMVar_hsa_circ_173744,RMVar_hsa_circ_173742 39256 RMVar_ID_39256 Human_SNP_ID_582722378 A-to-I Human chr15 + 72529370 72529370 72529370 GCTCAAACTGATTCTCTCGCCTCAGCCTCCCTAGTGGGTAGGACTGTGCACCACAACACCTAGCA GCTCAAACTGATTCTCTCGCCTCAGCCTCCCTGGTGGGTAGGACTGTGCACCACAACACCTAGCA A G ARIH1 Ensembl:ENSG00000166233 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054551671 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_173741,RMVar_hsa_circ_22124,RMVar_hsa_circ_173737,RMVar_hsa_circ_82587,RMVar_hsa_circ_173738,RMVar_hsa_circ_289375,RMVar_hsa_circ_307863,RMVar_hsa_circ_173736,RMVar_hsa_circ_309093,RMVar_hsa_circ_294931,RMVar_hsa_circ_279703,RMVar_hsa_circ_281490,RMVar_hsa_circ_270334,RMVar_hsa_circ_173743,RMVar_hsa_circ_173745,RMVar_hsa_circ_173746,RMVar_hsa_circ_173747,RMVar_hsa_circ_173744,RMVar_hsa_circ_173742 39257 RMVar_ID_39257 Human_SNP_ID_582722380 A-to-I Human chr15 + 72529377 72529377 72529377 CTGATTCTCTCGCCTCAGCCTCCCTAGTGGGTAGGACTGTGCACCACAACACCTAGCAAATTTTT CTGATTCTCTCGCCTCAGCCTCCCTAGTGGGTGGGACTGTGCACCACAACACCTAGCAAATTTTT A G ARIH1 Ensembl:ENSG00000166233 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1427298395 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8422088 RMVar_hsa_circ_173741,RMVar_hsa_circ_22124,RMVar_hsa_circ_173737,RMVar_hsa_circ_82587,RMVar_hsa_circ_173738,RMVar_hsa_circ_289375,RMVar_hsa_circ_307863,RMVar_hsa_circ_173736,RMVar_hsa_circ_309093,RMVar_hsa_circ_294931,RMVar_hsa_circ_279703,RMVar_hsa_circ_281490,RMVar_hsa_circ_270334,RMVar_hsa_circ_173743,RMVar_hsa_circ_173745,RMVar_hsa_circ_173746,RMVar_hsa_circ_173747,RMVar_hsa_circ_173744,RMVar_hsa_circ_173742 39258 RMVar_ID_39258 Human_SNP_ID_582723414 A-to-I Human chr15 + 72533697 72533697 72533697 GACTCAGCAACATGGGAGAATCGCTTGAGGCCAGGAGTTACAGATCAGCTTGGGCAACATAGTGA GACTCAGCAACATGGGAGAATCGCTTGAGGCCGGGAGTTACAGATCAGCTTGGGCAACATAGTGA A G ARIH1 Ensembl:ENSG00000166233 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1320721523 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_173741,RMVar_hsa_circ_22124,RMVar_hsa_circ_173737,RMVar_hsa_circ_82587,RMVar_hsa_circ_173738,RMVar_hsa_circ_289375,RMVar_hsa_circ_307863,RMVar_hsa_circ_173736,RMVar_hsa_circ_309093,RMVar_hsa_circ_294931,RMVar_hsa_circ_279703,RMVar_hsa_circ_281490,RMVar_hsa_circ_270334,RMVar_hsa_circ_173743,RMVar_hsa_circ_173745,RMVar_hsa_circ_173746,RMVar_hsa_circ_173747,RMVar_hsa_circ_173744,RMVar_hsa_circ_173742 39259 RMVar_ID_39259 Human_SNP_ID_582730212 A-to-I Human chr15 + 72561738 72561738 72561738 GTGTGGTGGCTCATGCCTGTAATCCCAGCACTAAGGGAGGCCGAGGCGGGTGGATCACCTGAGAT GTGTGGTGGCTCATGCCTGTAATCCCAGCACTTAGGGAGGCCGAGGCGGGTGGATCACCTGAGAT A T ARIH1 Ensembl:ENSG00000166233 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1209933066 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22650821,Human_RBP_ID_25163264 RMVar_hsa_circ_22868,RMVar_hsa_circ_22124,RMVar_hsa_circ_307863,RMVar_hsa_circ_173736,RMVar_hsa_circ_309093,RMVar_hsa_circ_294931,RMVar_hsa_circ_279703,RMVar_hsa_circ_173745,RMVar_hsa_circ_173746,RMVar_hsa_circ_173747,RMVar_hsa_circ_173744,RMVar_hsa_circ_173749,RMVar_hsa_circ_286529,RMVar_hsa_circ_296808,RMVar_hsa_circ_355253,RMVar_hsa_circ_305775,RMVar_hsa_circ_271075,RMVar_hsa_circ_173751,RMVar_hsa_circ_173752,RMVar_hsa_circ_173750,RMVar_hsa_circ_318711,RMVar_hsa_circ_173748,RMVar_hsa_circ_331645,RMVar_hsa_circ_313963,RMVar_hsa_circ_122192,RMVar_hsa_circ_112514,RMVar_hsa_circ_173757,RMVar_hsa_circ_71624,RMVar_hsa_circ_75803,RMVar_hsa_circ_173759,RMVar_hsa_circ_173758,RMVar_hsa_circ_173755,RMVar_hsa_circ_173756,RMVar_hsa_circ_85737,RMVar_hsa_circ_330529,RMVar_hsa_circ_44872,RMVar_hsa_circ_173762,RMVar_hsa_circ_173763,RMVar_hsa_circ_302076,RMVar_hsa_circ_322142,RMVar_hsa_circ_173764 39260 RMVar_ID_39260 Human_SNP_ID_582730526 A-to-I Human chr15 + 72563137 72563137 72563137 GCAGCAGATGATCACAGCTCTCTGCAGCCTCTACTTCCTGGGCTCAAGTGATCCTCTTGCCTCAG GCAGCAGATGATCACAGCTCTCTGCAGCCTCTGCTTCCTGGGCTCAAGTGATCCTCTTGCCTCAG A G ARIH1 Ensembl:ENSG00000166233 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1338765211 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22868,RMVar_hsa_circ_22124,RMVar_hsa_circ_307863,RMVar_hsa_circ_173736,RMVar_hsa_circ_309093,RMVar_hsa_circ_294931,RMVar_hsa_circ_279703,RMVar_hsa_circ_173745,RMVar_hsa_circ_173746,RMVar_hsa_circ_173747,RMVar_hsa_circ_173744,RMVar_hsa_circ_173749,RMVar_hsa_circ_286529,RMVar_hsa_circ_296808,RMVar_hsa_circ_355253,RMVar_hsa_circ_305775,RMVar_hsa_circ_271075,RMVar_hsa_circ_173751,RMVar_hsa_circ_173752,RMVar_hsa_circ_173750,RMVar_hsa_circ_318711,RMVar_hsa_circ_173748,RMVar_hsa_circ_331645,RMVar_hsa_circ_313963,RMVar_hsa_circ_122192,RMVar_hsa_circ_112514,RMVar_hsa_circ_173757,RMVar_hsa_circ_71624,RMVar_hsa_circ_75803,RMVar_hsa_circ_173759,RMVar_hsa_circ_173758,RMVar_hsa_circ_173755,RMVar_hsa_circ_173756,RMVar_hsa_circ_85737,RMVar_hsa_circ_330529,RMVar_hsa_circ_44872,RMVar_hsa_circ_173762,RMVar_hsa_circ_173763,RMVar_hsa_circ_302076,RMVar_hsa_circ_322142,RMVar_hsa_circ_173764 39261 RMVar_ID_39261 Human_SNP_ID_582730538 A-to-I Human chr15 + 72563190 72563190 72563190 CTCTTGCCTCAGCCTCCTGTGTAGTCGGGACTACAGGCACATACCACCATGCCTGGCTAAATTCT CTCTTGCCTCAGCCTCCTGTGTAGTCGGGACTGCAGGCACATACCACCATGCCTGGCTAAATTCT A G ARIH1 Ensembl:ENSG00000166233 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1163601193 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12581793 RMVar_hsa_circ_22868,RMVar_hsa_circ_22124,RMVar_hsa_circ_307863,RMVar_hsa_circ_173736,RMVar_hsa_circ_309093,RMVar_hsa_circ_294931,RMVar_hsa_circ_279703,RMVar_hsa_circ_173745,RMVar_hsa_circ_173746,RMVar_hsa_circ_173747,RMVar_hsa_circ_173744,RMVar_hsa_circ_173749,RMVar_hsa_circ_286529,RMVar_hsa_circ_296808,RMVar_hsa_circ_355253,RMVar_hsa_circ_305775,RMVar_hsa_circ_271075,RMVar_hsa_circ_173751,RMVar_hsa_circ_173752,RMVar_hsa_circ_173750,RMVar_hsa_circ_318711,RMVar_hsa_circ_173748,RMVar_hsa_circ_331645,RMVar_hsa_circ_313963,RMVar_hsa_circ_122192,RMVar_hsa_circ_112514,RMVar_hsa_circ_173757,RMVar_hsa_circ_71624,RMVar_hsa_circ_75803,RMVar_hsa_circ_173759,RMVar_hsa_circ_173758,RMVar_hsa_circ_173755,RMVar_hsa_circ_173756,RMVar_hsa_circ_85737,RMVar_hsa_circ_330529,RMVar_hsa_circ_44872,RMVar_hsa_circ_173762,RMVar_hsa_circ_173763,RMVar_hsa_circ_302076,RMVar_hsa_circ_322142,RMVar_hsa_circ_173764 39262 RMVar_ID_39262 Human_SNP_ID_582730560 A-to-I Human chr15 + 72563248 72563248 72563248 AAATTCTTTTTTCTTTTTTTTAAGGTAGAGACAAGGTCTTGCTATGTTGCCCGGGCTGGTCTGGA AAATTCTTTTTTCTTTTTTTTAAGGTAGAGACGAGGTCTTGCTATGTTGCCCGGGCTGGTCTGGA A G ARIH1 Ensembl:ENSG00000166233 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs139257534 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12581799 RMVar_hsa_circ_22868,RMVar_hsa_circ_22124,RMVar_hsa_circ_307863,RMVar_hsa_circ_173736,RMVar_hsa_circ_309093,RMVar_hsa_circ_294931,RMVar_hsa_circ_279703,RMVar_hsa_circ_173745,RMVar_hsa_circ_173746,RMVar_hsa_circ_173747,RMVar_hsa_circ_173744,RMVar_hsa_circ_173749,RMVar_hsa_circ_286529,RMVar_hsa_circ_296808,RMVar_hsa_circ_355253,RMVar_hsa_circ_305775,RMVar_hsa_circ_271075,RMVar_hsa_circ_173751,RMVar_hsa_circ_173752,RMVar_hsa_circ_173750,RMVar_hsa_circ_318711,RMVar_hsa_circ_173748,RMVar_hsa_circ_331645,RMVar_hsa_circ_313963,RMVar_hsa_circ_122192,RMVar_hsa_circ_112514,RMVar_hsa_circ_173757,RMVar_hsa_circ_71624,RMVar_hsa_circ_75803,RMVar_hsa_circ_173759,RMVar_hsa_circ_173758,RMVar_hsa_circ_173755,RMVar_hsa_circ_173756,RMVar_hsa_circ_85737,RMVar_hsa_circ_330529,RMVar_hsa_circ_44872,RMVar_hsa_circ_173762,RMVar_hsa_circ_173763,RMVar_hsa_circ_302076,RMVar_hsa_circ_322142,RMVar_hsa_circ_173764 39263 RMVar_ID_39263 Human_SNP_ID_582732679 A-to-I Human chr15 + 72572457 72572457 72572457 AGTCTAGTCTCGAACTCCTGACCTCGTGATCCACTGGCCTCGGCCTCCCAAAGTGCTGGGATTAC AGTCTAGTCTCGAACTCCTGACCTCGTGATCCGCTGGCCTCGGCCTCCCAAAGTGCTGGGATTAC A G ARIH1 Ensembl:ENSG00000166233 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs942001296 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22124,RMVar_hsa_circ_173747,RMVar_hsa_circ_355253,RMVar_hsa_circ_173748,RMVar_hsa_circ_122192,RMVar_hsa_circ_112514,RMVar_hsa_circ_173757,RMVar_hsa_circ_75803,RMVar_hsa_circ_173755,RMVar_hsa_circ_173756,RMVar_hsa_circ_82413,RMVar_hsa_circ_173765,RMVar_hsa_circ_106572,RMVar_hsa_circ_173772,RMVar_hsa_circ_96354,RMVar_hsa_circ_173774 39264 RMVar_ID_39264 Human_SNP_ID_582733593 A-to-I Human chr15 + 72576350 72576350 72576350 ACACAGTGAAACCCCATCTCTACTAAAAATACAAAAAAATTAGCTGGGCGTGGTGGCGGGCACCT ACACAGTGAAACCCCATCTCTACTAAAAATACGAAAAAATTAGCTGGGCGTGGTGGCGGGCACCT A G ARIH1 Ensembl:ENSG00000166233 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1393308132 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22124,RMVar_hsa_circ_173747,RMVar_hsa_circ_355253,RMVar_hsa_circ_173748,RMVar_hsa_circ_122192,RMVar_hsa_circ_112514,RMVar_hsa_circ_173757,RMVar_hsa_circ_75803,RMVar_hsa_circ_173755,RMVar_hsa_circ_173756,RMVar_hsa_circ_82413,RMVar_hsa_circ_173765,RMVar_hsa_circ_106572,RMVar_hsa_circ_173772,RMVar_hsa_circ_96354,RMVar_hsa_circ_173774 39265 RMVar_ID_39265 Human_SNP_ID_582733806 A-to-I Human chr15 + 72577082 72577082 72577082 TCAGCTCCCTGCAACCTCCACCTCCCGAATTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGT TCAGCTCCCTGCAACCTCCACCTCCCGAATTCTAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGT A T ARIH1 Ensembl:ENSG00000166233 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025708806 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22124,RMVar_hsa_circ_173747,RMVar_hsa_circ_355253,RMVar_hsa_circ_173748,RMVar_hsa_circ_122192,RMVar_hsa_circ_112514,RMVar_hsa_circ_173757,RMVar_hsa_circ_75803,RMVar_hsa_circ_173755,RMVar_hsa_circ_173756,RMVar_hsa_circ_82413,RMVar_hsa_circ_173765,RMVar_hsa_circ_106572,RMVar_hsa_circ_173772,RMVar_hsa_circ_96354,RMVar_hsa_circ_173774 39266 RMVar_ID_39266 Human_SNP_ID_582733831 A-to-I Human chr15 + 72577168 72577168 72577168 CCATGCCTGGCTAATTTTTTTGTATTTTTAGTAGAGACGGGATTTCATCATGTTGGTCAGGCTGG CCATGCCTGGCTAATTTTTTTGTATTTTTAGTGGAGACGGGATTTCATCATGTTGGTCAGGCTGG A G ARIH1 Ensembl:ENSG00000166233 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs539840056 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22124,RMVar_hsa_circ_173747,RMVar_hsa_circ_355253,RMVar_hsa_circ_173748,RMVar_hsa_circ_122192,RMVar_hsa_circ_112514,RMVar_hsa_circ_173757,RMVar_hsa_circ_75803,RMVar_hsa_circ_173755,RMVar_hsa_circ_173756,RMVar_hsa_circ_82413,RMVar_hsa_circ_173765,RMVar_hsa_circ_106572,RMVar_hsa_circ_173772,RMVar_hsa_circ_96354,RMVar_hsa_circ_173774 39267 RMVar_ID_39267 Human_SNP_ID_582733931 A-to-I Human chr15 + 72577562 72577562 72577562 GGGCGTGGTAGCAGGCGCCTGTAATCCGAGCTACTTGGGAAGATAAGGCAGGAGAATCACTTGAA GGGCGTGGTAGCAGGCGCCTGTAATCCGAGCTGCTTGGGAAGATAAGGCAGGAGAATCACTTGAA A G ARIH1 Ensembl:ENSG00000166233 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs528195818 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22124,RMVar_hsa_circ_173747,RMVar_hsa_circ_355253,RMVar_hsa_circ_173748,RMVar_hsa_circ_122192,RMVar_hsa_circ_112514,RMVar_hsa_circ_173757,RMVar_hsa_circ_75803,RMVar_hsa_circ_173755,RMVar_hsa_circ_173756,RMVar_hsa_circ_82413,RMVar_hsa_circ_173765,RMVar_hsa_circ_106572,RMVar_hsa_circ_173772,RMVar_hsa_circ_96354,RMVar_hsa_circ_173774 39268 RMVar_ID_39268 Human_SNP_ID_582734327 A-to-I Human chr15 + 72579058 72579048 72579059 CACCCGCCTCAGCCTCCCAAAGTGCTAGGATTACAGGCATGAGCCACCACACCCAGCCTATCTTA CACCCGCCTCAGCCTCCCAAAGT___________AGGCATGAGCCACCACACCCAGCCTATCTTA TGCTAGGATTAC T ARIH1 Ensembl:ENSG00000166233 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1344592795 Functional Loss DEL dbSNP153 24..34 33 - - - RMVar_hsa_circ_22124,RMVar_hsa_circ_173747,RMVar_hsa_circ_355253,RMVar_hsa_circ_173748,RMVar_hsa_circ_122192,RMVar_hsa_circ_112514,RMVar_hsa_circ_173757,RMVar_hsa_circ_75803,RMVar_hsa_circ_173755,RMVar_hsa_circ_173756,RMVar_hsa_circ_82413,RMVar_hsa_circ_173765,RMVar_hsa_circ_106572,RMVar_hsa_circ_173772,RMVar_hsa_circ_96354,RMVar_hsa_circ_173774 39269 RMVar_ID_39269 Human_SNP_ID_582736704 A-to-I Human chr15 + 72589858 72589858 72589858 TATTTTTTATTTTTTTAAGAGACAGTCTTGCTATGTTGCCCAGGCTGGACTTGAACTCCTAGTCT TATTTTTTATTTTTTTAAGAGACAGTCTTGCTGTGTTGCCCAGGCTGGACTTGAACTCCTAGTCT A G ARIH1,AC100827.3 Ensembl:ENSG00000166233,Ensembl:ENSG00000260534 Protein coding,lincRNA 3'UTR,exon GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs937726961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8183642,Human_RBP_ID_12582868,Human_RBP_ID_22799234 Human_miRNA_ID_1157425,Human_miRNA_ID_3207447,Human_miRNA_ID_3209355 39270 RMVar_ID_39270 Human_SNP_ID_582736867 A-to-I Human chr15 + 72590588 72590588 72590588 ACATGGGCTTTTTAAAAGATTACTATTTTTTTAGAGGTGGGGTCTCACTATGTTGCCCAGGCTGG ACATGGGCTTTTTAAAAGATTACTATTTTTTTGGAGGTGGGGTCTCACTATGTTGCCCAGGCTGG A G ARIH1,AC100827.3 Ensembl:ENSG00000166233,Ensembl:ENSG00000260534 Protein coding,lincRNA 3'UTR,exon GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1567364895 Functional Loss SNV dbSNP153 33..33 33 - - - 39271 RMVar_ID_39271 Human_SNP_ID_582736872 A-to-I Human chr15 + 72590605 72590605 72590605 GATTACTATTTTTTTAGAGGTGGGGTCTCACTATGTTGCCCAGGCTGGAATATAATGGCTATTCA GATTACTATTTTTTTAGAGGTGGGGTCTCACTGTGTTGCCCAGGCTGGAATATAATGGCTATTCA A G ARIH1,AC100827.3 Ensembl:ENSG00000166233,Ensembl:ENSG00000260534 Protein coding,lincRNA 3'UTR,exon GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs537837094 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17866067 39272 RMVar_ID_39272 Human_SNP_ID_582736894 A-to-I Human chr15 + 72590716 72590716 72590716 CCATCTTCCTGCCACAGCCTCCTGAGTAACCTAGGACTATAGGTGCATGCCACCATGCCCAGCTG CCATCTTCCTGCCACAGCCTCCTGAGTAACCTGGGACTATAGGTGCATGCCACCATGCCCAGCTG A G ARIH1,AC100827.3 Ensembl:ENSG00000166233,Ensembl:ENSG00000260534 Protein coding,lincRNA 3'UTR,exon GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs553948963 Functional Loss SNV dbSNP153 33..33 33 - - - 39273 RMVar_ID_39273 Human_SNP_ID_582736895 A-to-I Human chr15 + 72590722 72590722 72590722 TCCTGCCACAGCCTCCTGAGTAACCTAGGACTATAGGTGCATGCCACCATGCCCAGCTGACAATG TCCTGCCACAGCCTCCTGAGTAACCTAGGACTGTAGGTGCATGCCACCATGCCCAGCTGACAATG A G ARIH1,AC100827.3 Ensembl:ENSG00000166233,Ensembl:ENSG00000260534 Protein coding,lincRNA 3'UTR,exon GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs781672897 Functional Loss SNV dbSNP153 33..33 33 - - - 39274 RMVar_ID_39274 Human_SNP_ID_582736981 A-to-I Human chr15 + 72591101 72591101 72591101 AAAATTAGCCAGGCATGGTGGTGCATGCCTGTAATTCCAGCTGCTCGGAAGGCTGAGGCAGGAGA AAAATTAGCCAGGCATGGTGGTGCATGCCTGTGATTCCAGCTGCTCGGAAGGCTGAGGCAGGAGA A G ARIH1,AC100827.3 Ensembl:ENSG00000166233,Ensembl:ENSG00000260534 Protein coding,lincRNA 3'UTR,exon GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 29129909,30559470 RNA-Seq:(High) rs1133499 Functional Loss SNV dbSNP153 33..33 33 - - - 39275 RMVar_ID_39275 Human_SNP_ID_582744695 A-to-I Human chr15 + 72626441 72626440 72626442 ACCATCATGTCTGGCCTTTTTTTTTTTTTTTTAGATGAAGTTTTGCTCTTATTGCCCAGTACATA ACCATCATGTCTGGCCTTTTTTTTTTTTTTTT__ATGAAGTTTTGCTCTTATTGCCCAGTACATA TAG T lnc-ARIH1-1 RNACentral:URS00008B58A6 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs76785604 Functional Loss DEL dbSNP153 33..34 33 - - - 39276 RMVar_ID_39276 Human_SNP_ID_582744697 A-to-I Human chr15 + 72626441 72626440 72626441 ACCATCATGTCTGGCCTTTTTTTTTTTTTTTTAGATGAAGTTTTGCTCTTATTGCCCAGTACATA ACCATCATGTCTGGCCTTTTTTTTTTTTTTTT_GATGAAGTTTTGCTCTTATTGCCCAGTACATA TA T lnc-ARIH1-1 RNACentral:URS00008B58A6 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1433562976 Functional Loss DEL dbSNP153 33..33 33 - - - 39277 RMVar_ID_39277 Human_SNP_ID_582744698 A-to-I Human chr15 + 72626441 72626441 72626441 ACCATCATGTCTGGCCTTTTTTTTTTTTTTTTAGATGAAGTTTTGCTCTTATTGCCCAGTACATA ACCATCATGTCTGGCCTTTTTTTTTTTTTTTTTGATGAAGTTTTGCTCTTATTGCCCAGTACATA A T lnc-ARIH1-1 RNACentral:URS00008B58A6 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1392676020 Functional Loss SNV dbSNP153 33..33 33 - - - 39278 RMVar_ID_39278 Human_SNP_ID_582764160 A-to-I Human chr15 + 72719288 72719288 72719288 TTTCTAAATTTTTTTTTTTTTTTTTAAGAGACAAGGTTGCCTAGGCTGGAGTATAGTGGGGTGAT TTTCTAAATTTTTTTTTTTTTTTTTAAGAGACGAGGTTGCCTAGGCTGGAGTATAGTGGGGTGAT A G BBS4 Ensembl:ENSG00000140463 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335406178 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6460747,Human_RBP_ID_12584163 RMVar_hsa_circ_4485,RMVar_hsa_circ_364061,RMVar_hsa_circ_366329,RMVar_hsa_circ_310297,RMVar_hsa_circ_316853,RMVar_hsa_circ_8669,RMVar_hsa_circ_173779,RMVar_hsa_circ_323893,RMVar_hsa_circ_362669,RMVar_hsa_circ_369869,RMVar_hsa_circ_50378,RMVar_hsa_circ_173784,RMVar_hsa_circ_173782,RMVar_hsa_circ_173783,RMVar_hsa_circ_265080,RMVar_hsa_circ_365977 39279 RMVar_ID_39279 Human_SNP_ID_582764178 A-to-I Human chr15 + 72719354 72719354 72719354 ATAGCTTACTGTAACCTCCAACTCCTGGGCTCAAGTGATCCTCCTGCCTCTGCCTCCTGAGTAGC ATAGCTTACTGTAACCTCCAACTCCTGGGCTCGAGTGATCCTCCTGCCTCTGCCTCCTGAGTAGC A G BBS4 Ensembl:ENSG00000140463 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1267499761 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4485,RMVar_hsa_circ_364061,RMVar_hsa_circ_366329,RMVar_hsa_circ_310297,RMVar_hsa_circ_316853,RMVar_hsa_circ_8669,RMVar_hsa_circ_173779,RMVar_hsa_circ_323893,RMVar_hsa_circ_362669,RMVar_hsa_circ_369869,RMVar_hsa_circ_50378,RMVar_hsa_circ_173784,RMVar_hsa_circ_173782,RMVar_hsa_circ_173783,RMVar_hsa_circ_265080,RMVar_hsa_circ_365977 39280 RMVar_ID_39280 Human_SNP_ID_582764440 A-to-I Human chr15 + 72720368 72720368 72720368 ATTAGTGGTCGTGTGCACCTGTAGTCCTAGCTATTCTAGAGGCTGAGGTAGGAGGATCACGTTAG ATTAGTGGTCGTGTGCACCTGTAGTCCTAGCTCTTCTAGAGGCTGAGGTAGGAGGATCACGTTAG A C BBS4 Ensembl:ENSG00000140463 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs922518238 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12584185 RMVar_hsa_circ_4485,RMVar_hsa_circ_364061,RMVar_hsa_circ_366329,RMVar_hsa_circ_310297,RMVar_hsa_circ_316853,RMVar_hsa_circ_8669,RMVar_hsa_circ_173779,RMVar_hsa_circ_323893,RMVar_hsa_circ_362669,RMVar_hsa_circ_369869,RMVar_hsa_circ_50378,RMVar_hsa_circ_173784,RMVar_hsa_circ_173782,RMVar_hsa_circ_173783,RMVar_hsa_circ_265080,RMVar_hsa_circ_365977 39281 RMVar_ID_39281 Human_SNP_ID_582764441 A-to-I Human chr15 + 72720368 72720368 72720368 ATTAGTGGTCGTGTGCACCTGTAGTCCTAGCTATTCTAGAGGCTGAGGTAGGAGGATCACGTTAG ATTAGTGGTCGTGTGCACCTGTAGTCCTAGCTGTTCTAGAGGCTGAGGTAGGAGGATCACGTTAG A G BBS4 Ensembl:ENSG00000140463 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs922518238 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12584185 RMVar_hsa_circ_4485,RMVar_hsa_circ_364061,RMVar_hsa_circ_366329,RMVar_hsa_circ_310297,RMVar_hsa_circ_316853,RMVar_hsa_circ_8669,RMVar_hsa_circ_173779,RMVar_hsa_circ_323893,RMVar_hsa_circ_362669,RMVar_hsa_circ_369869,RMVar_hsa_circ_50378,RMVar_hsa_circ_173784,RMVar_hsa_circ_173782,RMVar_hsa_circ_173783,RMVar_hsa_circ_265080,RMVar_hsa_circ_365977 39282 RMVar_ID_39282 Human_SNP_ID_582766537 A-to-I Human chr15 + 72728407 72728407 72728407 GTAGTCCCAGCTACTTGGGAGGCTGTGATGGGAAGATTGCTTGAACTCGGAAGGCAGAGGTTGCA GTAGTCCCAGCTACTTGGGAGGCTGTGATGGGGAGATTGCTTGAACTCGGAAGGCAGAGGTTGCA A G BBS4 Ensembl:ENSG00000140463 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1004099374 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_162,RMVar_hsa_circ_364061,RMVar_hsa_circ_366329,RMVar_hsa_circ_8669,RMVar_hsa_circ_323893,RMVar_hsa_circ_50378,RMVar_hsa_circ_173784,RMVar_hsa_circ_173783,RMVar_hsa_circ_265080,RMVar_hsa_circ_365977,RMVar_hsa_circ_114529,RMVar_hsa_circ_340081,RMVar_hsa_circ_38297,RMVar_hsa_circ_173785 39283 RMVar_ID_39283 Human_SNP_ID_582778554 A-to-I Human chr15 - 72776222 72776222 72776222 GAACGTTCTCTTTAAAAGAGGGATGACTTAGCAAAGAAACCCTGAAAATGTAAGACAGACTTTCT GAACGTTCTCTTTAAAAGAGGGATGACTTAGCGAAGAAACCCTGAAAATGTAAGACAGACTTTCT T C ADPGK Ensembl:ENSG00000159322 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1009710627 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17563444 RMVar_hsa_circ_110375,RMVar_hsa_circ_173794,RMVar_hsa_circ_173790 39284 RMVar_ID_39284 Human_SNP_ID_582778556 A-to-I Human chr15 - 72776225 72776225 72776225 TTTGAACGTTCTCTTTAAAAGAGGGATGACTTAGCAAAGAAACCCTGAAAATGTAAGACAGACTT TTTGAACGTTCTCTTTAAAAGAGGGATGACTTCGCAAAGAAACCCTGAAAATGTAAGACAGACTT T G ADPGK Ensembl:ENSG00000159322 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs964416736 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17563444 RMVar_hsa_circ_110375,RMVar_hsa_circ_173794,RMVar_hsa_circ_173790 39285 RMVar_ID_39285 Human_SNP_ID_582779536 A-to-I Human chr15 - 72780613 72780613 72780613 TTTTATATTCTTGGTAGGGACAGGATTTGCCAAGTTGCTCAGGCTGGTCTTCAACTACTGGGATC TTTTATATTCTTGGTAGGGACAGGATTTGCCAGGTTGCTCAGGCTGGTCTTCAACTACTGGGATC T C ADPGK Ensembl:ENSG00000159322 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs191126825 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12585192 39286 RMVar_ID_39286 Human_SNP_ID_582779540 A-to-I Human chr15 - 72780641 72780641 72780641 CAGGCATGTACCACCACACCCGGCTAATTTTTATATTCTTGGTAGGGACAGGATTTGCCAAGTTG CAGGCATGTACCACCACACCCGGCTAATTTTTGTATTCTTGGTAGGGACAGGATTTGCCAAGTTG T C ADPGK Ensembl:ENSG00000159322 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1480106213 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12585192,Human_RBP_ID_18282034,Human_RBP_ID_23665484 39287 RMVar_ID_39287 Human_SNP_ID_582965382 A-to-I Human chr15 - 73566203 73566199 73566203 AGGGATATTGGAAAAGAAATGTGACTTTTAAAATGACACCTAAAACATGCATTCGGTGTCTGGTC AGGGATATTGGAAAAGAAATGTGACTTTTAAA____CACCTAAAACATGCATTCGGTGTCTGGTC GTCAT G NPTN Ensembl:ENSG00000156642 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1345197013 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_17866262 RMVar_hsa_circ_50441,RMVar_hsa_circ_321454,RMVar_hsa_circ_346902,RMVar_hsa_circ_173829 39288 RMVar_ID_39288 Human_SNP_ID_582965384 A-to-I Human chr15 - 73566203 73566203 73566203 AGGGATATTGGAAAAGAAATGTGACTTTTAAAATGACACCTAAAACATGCATTCGGTGTCTGGTC AGGGATATTGGAAAAGAAATGTGACTTTTAAAGTGACACCTAAAACATGCATTCGGTGTCTGGTC T C NPTN Ensembl:ENSG00000156642 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs539486358 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17866262 RMVar_hsa_circ_50441,RMVar_hsa_circ_321454,RMVar_hsa_circ_346902,RMVar_hsa_circ_173829 39289 RMVar_ID_39289 Human_SNP_ID_582975653 A-to-I Human chr15 - 73610270 73610270 73610270 TGTACAAAAAACGTAGCAAGACCCTCATCTCTACAAAAAACTAAAAAACTTAGCTGGGTGGGGTG TGTACAAAAAACGTAGCAAGACCCTCATCTCTGCAAAAAACTAAAAAACTTAGCTGGGTGGGGTG T C NPTN Ensembl:ENSG00000156642 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs895920906 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114789,RMVar_hsa_circ_173833 39290 RMVar_ID_39290 Human_SNP_ID_582979063 A-to-I Human chr15 - 73625460 73625460 73625460 AGGGGTGGTCGCCGGCACCTGTAGTCCCAGCTACTCGGGGCTGAGGCAGGAGAATGGCGTGAACC AGGGGTGGTCGCCGGCACCTGTAGTCCCAGCTGCTCGGGGCTGAGGCAGGAGAATGGCGTGAACC T C NPTN Ensembl:ENSG00000156642 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417988769 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12587896 RMVar_hsa_circ_114789,RMVar_hsa_circ_173833 39291 RMVar_ID_39291 Human_SNP_ID_582979412 A-to-I Human chr15 - 73627052 73627052 73627052 TTTTGGATTTTTAGTAGAAATGGAGTTTCGCCATGTTGGCCAGGCTGATCTCGAACTCCTGACCT TTTTGGATTTTTAGTAGAAATGGAGTTTCGCCGTGTTGGCCAGGCTGATCTCGAACTCCTGACCT T C NPTN Ensembl:ENSG00000156642 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1222330403 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114789,RMVar_hsa_circ_173833 39292 RMVar_ID_39292 Human_SNP_ID_583080791 A-to-I Human chr15 + 74025210 74025210 74025210 TTAGATGTGGGGTAGACAGTCGGCCACAGATCAGGGCTGCTGCAGAGGGAATTCCAGCATTAGAT TTAGATGTGGGGTAGACAGTCGGCCACAGATCGGGGCTGCTGCAGAGGGAATTCCAGCATTAGAT A G PML Ensembl:ENSG00000140464 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1409112222 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12588230 RMVar_hsa_circ_111015,RMVar_hsa_circ_173842 39293 RMVar_ID_39293 Human_SNP_ID_583081029 A-to-I Human chr15 + 74026288 74026288 74026288 CGCTTCCGGGGTTCAAGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCGCA CGCTTCCGGGGTTCAAGCCATTCTCCTGCCTCGGCCTCCCGAGTAGCTGGGACTACAGGCGCGCA A G PML Ensembl:ENSG00000140464 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1469833542 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111015,RMVar_hsa_circ_173842 39294 RMVar_ID_39294 Human_SNP_ID_583081267 A-to-I Human chr15 + 74027429 74027429 74027429 TAAAAATCAGCCAGGTGTGGTGGCACATGCCTATAATCCCAGGTACTCAGCAGGCTAAGGTGGGA TAAAAATCAGCCAGGTGTGGTGGCACATGCCTGTAATCCCAGGTACTCAGCAGGCTAAGGTGGGA A G PML Ensembl:ENSG00000140464 Protein coding intron GSE100210;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229 RNA-Seq:(High) rs966290930 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111015,RMVar_hsa_circ_173842 39295 RMVar_ID_39295 Human_SNP_ID_583157749 A-to-I Human chr15 - 74340599 74340598 74340599 TGTAAACAGCTTAGGACCCTGCCTGCCATATAATATATGCTTAATAAATGGTACCTCACAGCTTG TGTAAACAGCTTAGGACCCTGCCTGCCATATA_TATATGCTTAATAAATGGTACCTCACAGCTTG AT A CYP11A1 Ensembl:ENSG00000140459 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs71434231 Functional Loss DEL dbSNP153 33..33 33 - - - 39296 RMVar_ID_39296 Human_SNP_ID_583157875 A-to-I Human chr15 - 74341154 74341154 74341154 TAATACTCACAAACAACCCTCTAAGGTATGTTACCATCATCCCCCTTTTTCAGATGAGGAAAGTA TAATACTCACAAACAACCCTCTAAGGTATGTTGCCATCATCCCCCTTTTTCAGATGAGGAAAGTA T C CYP11A1 Ensembl:ENSG00000140459 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1166264798 Functional Loss SNV dbSNP153 33..33 33 - - - 39297 RMVar_ID_39297 Human_SNP_ID_583157898 A-to-I Human chr15 + 74341243 74341243 74341243 TTAGGACCCTGCCTGCCATATAGTATGTGCTTAATAAATGTGACCTCACAGTAATCGTTTCTTTG TTAGGACCCTGCCTGCCATATAGTATGTGCTTCATAAATGTGACCTCACAGTAATCGTTTCTTTG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1197538620 Functional Loss SNV dbSNP153 33..33 33 - - - 39298 RMVar_ID_39298 Human_SNP_ID_583157899 A-to-I Human chr15 + 74341243 74341243 74341243 TTAGGACCCTGCCTGCCATATAGTATGTGCTTAATAAATGTGACCTCACAGTAATCGTTTCTTTG TTAGGACCCTGCCTGCCATATAGTATGTGCTTGATAAATGTGACCTCACAGTAATCGTTTCTTTG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1197538620 Functional Loss SNV dbSNP153 33..33 33 - - - 39299 RMVar_ID_39299 Human_SNP_ID_583162317 A-to-I Human chr15 - 74360397 74360397 74360397 GGGCGTCTGTAATTCCAGCTACTCAGGAGGCTAGGGCAGAGAATTGCTTGAATCTGGGAGATGGA GGGCGTCTGTAATTCCAGCTACTCAGGAGGCTGGGGCAGAGAATTGCTTGAATCTGGGAGATGGA T C CYP11A1 Ensembl:ENSG00000140459 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs952757734 Functional Loss SNV dbSNP153 33..33 33 - - - 39300 RMVar_ID_39300 Human_SNP_ID_583162387 A-to-I Human chr15 - 74360723 74360723 74360723 AATTTTGTATTTTTACTAGAGATGGGGGTTTCACCATGTTGGTCAGGCTGGTCTTGAACTCCTGA AATTTTGTATTTTTACTAGAGATGGGGGTTTCGCCATGTTGGTCAGGCTGGTCTTGAACTCCTGA T C CYP11A1 Ensembl:ENSG00000140459 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1370455548 Functional Loss SNV dbSNP153 33..33 33 - - - 39301 RMVar_ID_39301 Human_SNP_ID_583188094 A-to-I Human chr15 + 74465246 74465246 74465246 GTTGCCCAGGCCGGTCTTGAATTACTGGACTCAAGCAATCTGCCCACCTCAGCCTCCCAAAGTAA GTTGCCCAGGCCGGTCTTGAATTACTGGACTCGAGCAATCTGCCCACCTCAGCCTCCCAAAGTAA A G UBL7-AS1 Ensembl:ENSG00000247240 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs915783048 Functional Loss SNV dbSNP153 33..33 33 - - - 39302 RMVar_ID_39302 Human_SNP_ID_583188270 A-to-I Human chr15 + 74466087 74466087 74466087 ATCTTGGCTCACTGCATCTCCACCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGCAGC ATCTTGGCTCACTGCATCTCCACCCCAGGTTCGAGCGATTCTCCTGCCTCAGCCTCCCAAGCAGC A G UBL7-AS1 Ensembl:ENSG00000247240 lincRNA exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1171680477 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_123869 Human_Splice_Rec_1625634,Human_Splice_Rec_1625635,Human_Splice_Rec_1625638,Human_Splice_Rec_1625639,Human_Splice_Rec_1625644,Human_Splice_Rec_1625645,Human_Splice_Rec_1625650,Human_Splice_Rec_1625651,Human_Splice_Rec_1625656,Human_Splice_Rec_1625657,Human_Splice_Rec_1625660,Human_Splice_Rec_1625661,Human_Splice_Rec_1625670,Human_Splice_Rec_1625671,Human_Splice_Rec_1625678,Human_Splice_Rec_1625679 RMVar_hsa_circ_99956,RMVar_hsa_circ_116677,RMVar_hsa_circ_173863,RMVar_hsa_circ_173864 39303 RMVar_ID_39303 Human_SNP_ID_583189783 A-to-I Human chr15 + 74473146 74473146 74473146 AAAATTAGCCAGGCATGGTGGCGGGTGCCTATAATCCCAGCTAATCTGGTGGCTGAGGCAGGAGA AAAATTAGCCAGGCATGGTGGCGGGTGCCTATGATCCCAGCTAATCTGGTGGCTGAGGCAGGAGA A G UBL7-AS1 Ensembl:ENSG00000247240 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs762794120 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8251699 RMVar_hsa_circ_116677,RMVar_hsa_circ_173863 39304 RMVar_ID_39304 Human_SNP_ID_583189990 A-to-I Human chr15 + 74474174 74474174 74474174 ACAGCTCACTGCAGCCTTGACCTCCTGGGCTCAAGTCATCCTCCCACCTCAGCCTCTCAAGTAGC ACAGCTCACTGCAGCCTTGACCTCCTGGGCTCCAGTCATCCTCCCACCTCAGCCTCTCAAGTAGC A C UBL7-AS1 Ensembl:ENSG00000247240 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs567353890 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116677,RMVar_hsa_circ_173863 39305 RMVar_ID_39305 Human_SNP_ID_583197199 A-to-I Human chr15 + 74505142 74505142 74505142 TAGGCTAGAGTGCGGTGGTGCAATCATAGCTCACGGCAACCTTGACCTCCTGGGCTCAAGTGATT TAGGCTAGAGTGCGGTGGTGCAATCATAGCTCGCGGCAACCTTGACCTCCTGGGCTCAAGTGATT A G UBL7-AS1,AC012435.3 Ensembl:ENSG00000247240,Ensembl:ENSG00000261775 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs751831037 Functional Loss SNV dbSNP153 33..33 33 - - - 39306 RMVar_ID_39306 Human_SNP_ID_583198142 A-to-I Human chr15 + 74509243 74509243 74509243 GGGCTCAAGTGGTCTTCCTGCCTCAGCCTCTCAAGTAGCTGGGACTACAGACATGTGCCACCATG GGGCTCAAGTGGTCTTCCTGCCTCAGCCTCTCCAGTAGCTGGGACTACAGACATGTGCCACCATG A C UBL7-AS1,AC012435.3 Ensembl:ENSG00000247240,Ensembl:ENSG00000261775 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1187901385 Functional Loss SNV dbSNP153 33..33 33 - - - 39307 RMVar_ID_39307 Human_SNP_ID_583208119 A-to-I Human chr15 + 74549122 74549122 74549122 TTTTTAGACGGTGTCTCGCTGTCACTCAGGCTAGAGTGCAGTGGCATGATCTCGGCTCACTGCAG TTTTTAGACGGTGTCTCGCTGTCACTCAGGCTGGAGTGCAGTGGCATGATCTCGGCTCACTGCAG A G ARID3B Ensembl:ENSG00000179361 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs755472735 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6804,RMVar_hsa_circ_173865,RMVar_hsa_circ_97246,RMVar_hsa_circ_345686,RMVar_hsa_circ_3669 39308 RMVar_ID_39308 Human_SNP_ID_583214374 A-to-I Human chr15 + 74573931 74573931 74573931 ACCTGGCTAATTTTTGTATTTCTTTTTTCAGTAGAGTTGGGGTTTCACCATGTTGGCCAGGCTGG ACCTGGCTAATTTTTGTATTTCTTTTTTCAGTGGAGTTGGGGTTTCACCATGTTGGCCAGGCTGG A G ARID3B Ensembl:ENSG00000179361 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1431438739 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_123592 RMVar_hsa_circ_173865,RMVar_hsa_circ_97246,RMVar_hsa_circ_3669,RMVar_hsa_circ_173868,RMVar_hsa_circ_376065 39309 RMVar_ID_39309 Human_SNP_ID_583214955 A-to-I Human chr15 + 74576537 74576537 74576537 AAAATTAGCCAGGCATAGTGATGCATGCCTGTAGTCCCAAGCTACTTGGGAGGCTGAGGTGGGCA AAAATTAGCCAGGCATAGTGATGCATGCCTGTCGTCCCAAGCTACTTGGGAGGCTGAGGTGGGCA A C ARID3B Ensembl:ENSG00000179361 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs752705503 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_173865,RMVar_hsa_circ_97246,RMVar_hsa_circ_3669,RMVar_hsa_circ_173868,RMVar_hsa_circ_376065 39310 RMVar_ID_39310 Human_SNP_ID_583216453 A-to-I Human chr15 + 74582307 74582307 74582307 CTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTATAGGCGCCTGCCACCACGTCTGGCTAATTTTT CTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTGTAGGCGCCTGCCACCACGTCTGGCTAATTTTT A G ARID3B Ensembl:ENSG00000179361 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1220005968 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_173865,RMVar_hsa_circ_97246,RMVar_hsa_circ_3669,RMVar_hsa_circ_173868,RMVar_hsa_circ_376065 39311 RMVar_ID_39311 Human_SNP_ID_583230850 A-to-I Human chr15 - 74639628 74639628 74639628 TCACTGCAACTTCCACCTCCTGAGCTTGAGCAATTCTCCCACCTCAGCCTCATGAAGTAGCTGAG TCACTGCAACTTCCACCTCCTGAGCTTGAGCAGTTCTCCCACCTCAGCCTCATGAAGTAGCTGAG T C EDC3 Ensembl:ENSG00000179151 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs764260836 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11548,RMVar_hsa_circ_52538,RMVar_hsa_circ_305729,RMVar_hsa_circ_23128,RMVar_hsa_circ_173881 39312 RMVar_ID_39312 Human_SNP_ID_583239467 A-to-I Human chr15 - 74677444 74677444 74677444 CAGGAGAATTGATTGAAGAGGCAGAGGCTGCAATGAGCTGAGATTGTACCACTGCACTCTAGCCT CAGGAGAATTGATTGAAGAGGCAGAGGCTGCATTGAGCTGAGATTGTACCACTGCACTCTAGCCT T A EDC3 Ensembl:ENSG00000179151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs969855321 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12590203,Human_RBP_ID_25165281 RMVar_hsa_circ_94834,RMVar_hsa_circ_173888,RMVar_hsa_circ_84511,RMVar_hsa_circ_173889 39313 RMVar_ID_39313 Human_SNP_ID_583239468 A-to-I Human chr15 - 74677444 74677444 74677444 CAGGAGAATTGATTGAAGAGGCAGAGGCTGCAATGAGCTGAGATTGTACCACTGCACTCTAGCCT CAGGAGAATTGATTGAAGAGGCAGAGGCTGCAGTGAGCTGAGATTGTACCACTGCACTCTAGCCT T C EDC3 Ensembl:ENSG00000179151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs969855321 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12590203,Human_RBP_ID_25165281 RMVar_hsa_circ_94834,RMVar_hsa_circ_173888,RMVar_hsa_circ_84511,RMVar_hsa_circ_173889 39314 RMVar_ID_39314 Human_SNP_ID_583239961 A-to-I Human chr15 - 74679676 74679676 74679676 GCCTCAAGCTATCCTCCCACCTTGGCCTCTCAAAGTGCTGGGATTACAGGTGTGAGCCACTGAGC GCCTCAAGCTATCCTCCCACCTTGGCCTCTCAGAGTGCTGGGATTACAGGTGTGAGCCACTGAGC T C EDC3 Ensembl:ENSG00000179151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1353504424 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94834,RMVar_hsa_circ_173888,RMVar_hsa_circ_84511,RMVar_hsa_circ_173889 39315 RMVar_ID_39315 Human_SNP_ID_583239962 A-to-I Human chr15 - 74679676 74679676 74679676 GCCTCAAGCTATCCTCCCACCTTGGCCTCTCAAAGTGCTGGGATTACAGGTGTGAGCCACTGAGC GCCTCAAGCTATCCTCCCACCTTGGCCTCTCACAGTGCTGGGATTACAGGTGTGAGCCACTGAGC T G EDC3 Ensembl:ENSG00000179151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1353504424 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94834,RMVar_hsa_circ_173888,RMVar_hsa_circ_84511,RMVar_hsa_circ_173889 39316 RMVar_ID_39316 Human_SNP_ID_583240028 A-to-I Human chr15 - 74679810 74679810 74679810 CTCCCTTCCTGCCTCAGGCTCCCAAGTAGCTGAGATTACTGGTATGCACCACTACACCTGTTTTT CTCCCTTCCTGCCTCAGGCTCCCAAGTAGCTGGGATTACTGGTATGCACCACTACACCTGTTTTT T C EDC3 Ensembl:ENSG00000179151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037971529 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1626119 RMVar_hsa_circ_94834,RMVar_hsa_circ_173888,RMVar_hsa_circ_84511,RMVar_hsa_circ_173889 39317 RMVar_ID_39317 Human_SNP_ID_583241051 A-to-I Human chr15 - 74683992 74683992 74683992 GGAGTGCAGTGGTACAATCATAGCTCACTGTAACCTCAAACTCCTGAGCTCTGTGATCTTCTTGC GGAGTGCAGTGGTACAATCATAGCTCACTGTATCCTCAAACTCCTGAGCTCTGTGATCTTCTTGC T A EDC3 Ensembl:ENSG00000179151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005486223 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94834,RMVar_hsa_circ_173888,RMVar_hsa_circ_84511,RMVar_hsa_circ_173889 39318 RMVar_ID_39318 Human_SNP_ID_583241345 A-to-I Human chr15 - 74685138 74685138 74685138 TGCCCACCTTAGCCTCCCAGAATGCTGAGATTACAGGCATGAACCACCATGCCTGACCAACACAC TGCCCACCTTAGCCTCCCAGAATGCTGAGATTGCAGGCATGAACCACCATGCCTGACCAACACAC T C EDC3 Ensembl:ENSG00000179151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs967351529 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94834,RMVar_hsa_circ_173888,RMVar_hsa_circ_84511,RMVar_hsa_circ_173889 39319 RMVar_ID_39319 Human_SNP_ID_583241799 A-to-I Human chr15 - 74686977 74686977 74686977 CAGGCTGGAGTGCAGTGGTGCGGTGTCGGCTCACTGCAGGCTCCGCCTCTTGGGTTCAAGCAGTT CAGGCTGGAGTGCAGTGGTGCGGTGTCGGCTCGCTGCAGGCTCCGCCTCTTGGGTTCAAGCAGTT T C EDC3 Ensembl:ENSG00000179151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1004861103 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94834,RMVar_hsa_circ_173888,RMVar_hsa_circ_84511,RMVar_hsa_circ_173889 39320 RMVar_ID_39320 Human_SNP_ID_583242200 A-to-I Human chr15 - 74688723 74688723 74688723 TTTTGTATTTTTAGTAGAGACAGGGTTTTGCCATGTTGGCTAGATTGGTATTGAACTCTTGACCT TTTTGTATTTTTAGTAGAGACAGGGTTTTGCCGTGTTGGCTAGATTGGTATTGAACTCTTGACCT T C EDC3 Ensembl:ENSG00000179151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053061187 Functional Loss SNV dbSNP153 33..33 33 - - - 39321 RMVar_ID_39321 Human_SNP_ID_583242202 A-to-I Human chr15 - 74688734 74688733 74688735 CCCAGCTAATTTTTTGTATTTTTAGTAGAGACAGGGTTTTGCCATGTTGGCTAGATTGGTATTGA CCCAGCTAATTTTTTGTATTTTTAGTAGAGA__GGGTTTTGCCATGTTGGCTAGATTGGTATTGA CTG C EDC3 Ensembl:ENSG00000179151 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1185128500 Functional Loss DEL dbSNP153 32..33 33 - - - 39322 RMVar_ID_39322 Human_SNP_ID_583270989 A-to-I Human chr15 + 74797059 74797059 74797059 ACCTCCCCAGGCTCAAGCGATCCTCCCACCTCAGCCTCCTGAGTAGCTGGGAGTACAAGCACGCA ACCTCCCCAGGCTCAAGCGATCCTCCCACCTCGGCCTCCTGAGTAGCTGGGAGTACAAGCACGCA A G CSK Ensembl:ENSG00000103653 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs914563531 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126688,RMVar_hsa_circ_173891 39323 RMVar_ID_39323 Human_SNP_ID_583271080 A-to-I Human chr15 + 74797409 74797409 74797409 GAAACCCCATCTCTACTGAAAATACAAAAATTAGCTGGTTGTGGTGGTGCATGCCTGTAATCCCA GAAACCCCATCTCTACTGAAAATACAAAAATTCGCTGGTTGTGGTGGTGCATGCCTGTAATCCCA A C CSK Ensembl:ENSG00000103653 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs960656555 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126688,RMVar_hsa_circ_173891 39324 RMVar_ID_39324 Human_SNP_ID_583284879 A-to-I Human chr15 - 74845564 74845564 74845564 TAGCGGTTGGATTGCAGCCCTGTCTACACTGGATAATCATTCCCTGGCCATATCAGTCATCATGA TAGCGGTTGGATTGCAGCCCTGTCTACACTGGGTAATCATTCCCTGGCCATATCAGTCATCATGA T C SCAMP2 Ensembl:ENSG00000140497 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1329047389 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_463625,Human_RBP_ID_1175834,Human_RBP_ID_1508409,Human_RBP_ID_8422663,Human_RBP_ID_9371773,Human_RBP_ID_12591203,Human_RBP_ID_17251108,Human_RBP_ID_17366312,Human_RBP_ID_17866552,Human_RBP_ID_18282182,Human_RBP_ID_22581062,Human_RBP_ID_22759656,Human_RBP_ID_27654657 Human_Splice_Rec_1627004,Human_Splice_Rec_1627005,Human_Splice_Rec_1627018,Human_Splice_Rec_1627022,Human_Splice_Rec_1627023,Human_Splice_Rec_1627036,Human_Splice_Rec_1627037,Human_Splice_Rec_1627046,Human_Splice_Rec_1627047,Human_Splice_Rec_1627062,Human_Splice_Rec_1627063 Human_miRNA_ID_2175522,Human_miRNA_ID_2178966 RMVar_hsa_circ_173901,RMVar_hsa_circ_76019,RMVar_hsa_circ_118372,RMVar_hsa_circ_173902,RMVar_hsa_circ_173903,RMVar_hsa_circ_361506 39325 RMVar_ID_39325 Human_SNP_ID_583284965 A-to-I Human chr15 - 74845923 74845923 74845923 GAACTCTTGGGCTCAAGCGATCCTCCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGAGAG GAACTCTTGGGCTCAAGCGATCCTCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGAGAG T C SCAMP2 Ensembl:ENSG00000140497 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11635885 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_173901,RMVar_hsa_circ_76019,RMVar_hsa_circ_118372,RMVar_hsa_circ_173902 39326 RMVar_ID_39326 Human_SNP_ID_583284995 A-to-I Human chr15 - 74846065 74846065 74846065 TTGGCCAGGCTGGTCTCAAACTCCTGACCTCAAGTGATCTGCCTTCCTTGGCCTCCCAAAGTGCT TTGGCCAGGCTGGTCTCAAACTCCTGACCTCAGGTGATCTGCCTTCCTTGGCCTCCCAAAGTGCT T C SCAMP2 Ensembl:ENSG00000140497 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs995966622 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_173901,RMVar_hsa_circ_76019,RMVar_hsa_circ_118372,RMVar_hsa_circ_173902 39327 RMVar_ID_39327 Human_SNP_ID_583285179 A-to-I Human chr15 - 74846702 74846702 74846702 GGAGTGCAGTGCCGCGATCTCTGCTCACTGCAAGCTCCGCCTCCCAGGTTCACGCCATTCTCCTG GGAGTGCAGTGCCGCGATCTCTGCTCACTGCACGCTCCGCCTCCCAGGTTCACGCCATTCTCCTG T G SCAMP2 Ensembl:ENSG00000140497 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs558521322 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_173901,RMVar_hsa_circ_76019,RMVar_hsa_circ_118372,RMVar_hsa_circ_173902 39328 RMVar_ID_39328 Human_SNP_ID_583285316 A-to-I Human chr15 - 74847220 74847220 74847220 AGGCGCATTGGTAGGTGCCTATAATCCCAGCTACTTGGGAGGCTGAGGCAGAAGAATCACTTGAA AGGCGCATTGGTAGGTGCCTATAATCCCAGCTCCTTGGGAGGCTGAGGCAGAAGAATCACTTGAA T G SCAMP2 Ensembl:ENSG00000140497 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs144388245 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_173901,RMVar_hsa_circ_76019,RMVar_hsa_circ_118372,RMVar_hsa_circ_173902 39329 RMVar_ID_39329 Human_SNP_ID_583285321 A-to-I Human chr15 - 74847229 74847229 74847229 AAATTGGCCAGGCGCATTGGTAGGTGCCTATAATCCCAGCTACTTGGGAGGCTGAGGCAGAAGAA AAATTGGCCAGGCGCATTGGTAGGTGCCTATAGTCCCAGCTACTTGGGAGGCTGAGGCAGAAGAA T C SCAMP2 Ensembl:ENSG00000140497 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1356206449 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_173901,RMVar_hsa_circ_76019,RMVar_hsa_circ_118372,RMVar_hsa_circ_173902 39330 RMVar_ID_39330 Human_SNP_ID_583290387 A-to-I Human chr15 - 74866546 74866546 74866546 TAGCATGCCTGGCTAATTTTTGTATTTTTCGTAGAGGTGGGGTTTCAACCACGTTGGTCAGGCTG TAGCATGCCTGGCTAATTTTTGTATTTTTCGTGGAGGTGGGGTTTCAACCACGTTGGTCAGGCTG T C SCAMP2 Ensembl:ENSG00000140497 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749421412 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118372,RMVar_hsa_circ_173902,RMVar_hsa_circ_111829,RMVar_hsa_circ_173904 39331 RMVar_ID_39331 Human_SNP_ID_583290858 A-to-I Human chr15 - 74868823 74868823 74868823 TTCACAAGGCTTGGCCAGGCATGGTGGCTCACACCTATAATCTCAGCAATTTGGGAGGCCAAGGC TTCACAAGGCTTGGCCAGGCATGGTGGCTCACGCCTATAATCTCAGCAATTTGGGAGGCCAAGGC T C SCAMP2 Ensembl:ENSG00000140497 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1307924059 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118372,RMVar_hsa_circ_173902,RMVar_hsa_circ_111829,RMVar_hsa_circ_173904 39332 RMVar_ID_39332 Human_SNP_ID_583290917 A-to-I Human chr15 - 74869092 74869092 74869092 TAGAGTGCAATGGTGCGATCTTGGCTCACTGCAGTCTCCACCTCCTGGGTTCAAGCGATTCTCCT TAGAGTGCAATGGTGCGATCTTGGCTCACTGCGGTCTCCACCTCCTGGGTTCAAGCGATTCTCCT T C SCAMP2 Ensembl:ENSG00000140497 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs558451244 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118372,RMVar_hsa_circ_173902,RMVar_hsa_circ_111829,RMVar_hsa_circ_173904 39333 RMVar_ID_39333 Human_SNP_ID_583298010 A-to-I Human chr15 + 74894440 74894440 74894440 GGCTGGGCACGGTGGCTCACACCTGTAATCCTAACACTTTGGGAGGTTGAGGCGGCCGTATCACT GGCTGGGCACGGTGGCTCACACCTGTAATCCTGACACTTTGGGAGGTTGAGGCGGCCGTATCACT A G MPI Ensembl:ENSG00000178802 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs571353058 Functional Loss SNV dbSNP153 33..33 33 - - - 39334 RMVar_ID_39334 Human_SNP_ID_583298020 A-to-I Human chr15 + 74894503 74894503 74894503 CTTGAGGTCAGGAATTCAAGACCAGCCTGGCCAACATGGTGGAACCCCATCTCTACTAAAGATAC CTTGAGGTCAGGAATTCAAGACCAGCCTGGCCGACATGGTGGAACCCCATCTCTACTAAAGATAC A G MPI Ensembl:ENSG00000178802 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1048888754 Functional Loss SNV dbSNP153 33..33 33 - - - 39335 RMVar_ID_39335 Human_SNP_ID_583306177 A-to-I Human chr15 - 74924469 74924469 74924469 TCCCCTAGGCTGGAGTGTAGTGTCATGATCTCAGCTCACTGCAACCTCCGCCTCCCTAGTTCAAG TCCCCTAGGCTGGAGTGTAGTGTCATGATCTCTGCTCACTGCAACCTCCGCCTCCCTAGTTCAAG T A COX5A Ensembl:ENSG00000178741 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs565316892 Functional Loss SNV dbSNP153 33..33 33 - - - 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_277277,RMVar_hsa_circ_173916,RMVar_hsa_circ_173917,RMVar_hsa_circ_173915 39336 RMVar_ID_39336 Human_SNP_ID_583306364 A-to-I Human chr15 - 74925213 74925213 74925213 CTGCAACCTCCGAGGTCTCCTGGGTTCAAGCAATTCTTCTGCCTCAGCCTCCCGAGTAGCTGGGA CTGCAACCTCCGAGGTCTCCTGGGTTCAAGCAGTTCTTCTGCCTCAGCCTCCCGAGTAGCTGGGA T C COX5A Ensembl:ENSG00000178741 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs984395212 Functional Loss SNV dbSNP153 33..33 33 - - - 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_277277,RMVar_hsa_circ_173916,RMVar_hsa_circ_173917,RMVar_hsa_circ_173915 39337 RMVar_ID_39337 Human_SNP_ID_583306433 A-to-I Human chr15 - 74925467 74925467 74925467 GGGGAATTGCTTGAACCCGGGAGGCAGAGGTTACAGTGAGCCAAGATGGCACCATTGCACTCCAG GGGGAATTGCTTGAACCCGGGAGGCAGAGGTTGCAGTGAGCCAAGATGGCACCATTGCACTCCAG T C COX5A Ensembl:ENSG00000178741 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1381067692 Functional Loss SNV dbSNP153 33..33 33 - - - 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_277277,RMVar_hsa_circ_173916,RMVar_hsa_circ_173917,RMVar_hsa_circ_173915 39338 RMVar_ID_39338 Human_SNP_ID_583307016 A-to-I Human chr15 - 74927623 74927623 74927623 GAATTACAGGCATGTGCCACCACGCCCGGCCAATTTTGTATCTTTAATAGAGACAGGGTTTCTCC GAATTACAGGCATGTGCCACCACGCCCGGCCAGTTTTGTATCTTTAATAGAGACAGGGTTTCTCC T C COX5A Ensembl:ENSG00000178741 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1311869673 Functional Loss SNV dbSNP153 33..33 33 - - - 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 39339 RMVar_ID_39339 Human_SNP_ID_583307858 A-to-I Human chr15 - 74930653 74930653 74930653 GAACTTGAATGGTGCCAGGGCTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGCCAAGGGA GAACTTGAATGGTGCCAGGGCTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGCCAAGGGA T C COX5A Ensembl:ENSG00000178741 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1448800082 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17563286 RMVar_hsa_circ_112108,RMVar_hsa_circ_90015,RMVar_hsa_circ_173914,RMVar_hsa_circ_173915,RMVar_hsa_circ_95908,RMVar_hsa_circ_173920 39340 RMVar_ID_39340 Human_SNP_ID_583308051 A-to-I Human chr15 - 74931266 74931266 74931266 AAACTCCTGAACTCAGGTGATCCACCAGTCTCAGCCTCCCAAAGTGCTGGCATTACAGGTGTGAG AAACTCCTGAACTCAGGTGATCCACCAGTCTCGGCCTCCCAAAGTGCTGGCATTACAGGTGTGAG T C COX5A Ensembl:ENSG00000178741 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991014748 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112108,RMVar_hsa_circ_90015,RMVar_hsa_circ_173914,RMVar_hsa_circ_173915,RMVar_hsa_circ_95908,RMVar_hsa_circ_173920 39341 RMVar_ID_39341 Human_SNP_ID_583308161 A-to-I Human chr15 - 74931659 74931659 74931659 GTCTCAGCTACTCAGAAGGCTGAGGCAGGAGAATCACTTGAATCCAGGAGGCAGAGGTTGCAGTG GTCTCAGCTACTCAGAAGGCTGAGGCAGGAGACTCACTTGAATCCAGGAGGCAGAGGTTGCAGTG T G COX5A Ensembl:ENSG00000178741 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1232213923 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112108,RMVar_hsa_circ_90015,RMVar_hsa_circ_173914,RMVar_hsa_circ_173915,RMVar_hsa_circ_95908,RMVar_hsa_circ_173920 39342 RMVar_ID_39342 Human_SNP_ID_583308203 A-to-I Human chr15 - 74931827 74931827 74931827 AAATGGGGCTGGGTGCAGTGGCTCGCGTCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGCAG AAATGGGGCTGGGTGCAGTGGCTCGCGTCTGTCATCCCAGCACTTTGGGAGGCTGAGGTGGGCAG T G COX5A Ensembl:ENSG00000178741 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1156956542 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112108,RMVar_hsa_circ_90015,RMVar_hsa_circ_173914,RMVar_hsa_circ_173915,RMVar_hsa_circ_95908,RMVar_hsa_circ_173920 39343 RMVar_ID_39343 Human_SNP_ID_583308440 A-to-I Human chr15 - 74932924 74932924 74932924 TGGGAGGCCGAGGCAGGCAGATCATGAGGTCAAGAGTTCGAGACCAGCCTGACTAACATGGTGAA TGGGAGGCCGAGGCAGGCAGATCATGAGGTCAGGAGTTCGAGACCAGCCTGACTAACATGGTGAA T C COX5A Ensembl:ENSG00000178741 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1566981645 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112108,RMVar_hsa_circ_90015,RMVar_hsa_circ_173914,RMVar_hsa_circ_173915,RMVar_hsa_circ_95908,RMVar_hsa_circ_173920 39344 RMVar_ID_39344 Human_SNP_ID_583309077 A-to-I Human chr15 - 74935284 74935282 74935284 TTTTGTTTTGTTTTTGTTTTTGTTTTTGAGACAGGGTCTCGCTCTGTCATGCAGGCTGCAGTGCA TTTTGTTTTGTTTTTGTTTTTGTTTTTGAGAC__GGTCTCGCTCTGTCATGCAGGCTGCAGTGCA CCT C COX5A Ensembl:ENSG00000178741 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1348072752 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_112108,RMVar_hsa_circ_90015,RMVar_hsa_circ_173914,RMVar_hsa_circ_173915,RMVar_hsa_circ_95908,RMVar_hsa_circ_173920 39345 RMVar_ID_39345 Human_SNP_ID_583309078 A-to-I Human chr15 - 74935284 74935284 74935284 TTTTGTTTTGTTTTTGTTTTTGTTTTTGAGACAGGGTCTCGCTCTGTCATGCAGGCTGCAGTGCA TTTTGTTTTGTTTTTGTTTTTGTTTTTGAGACGGGGTCTCGCTCTGTCATGCAGGCTGCAGTGCA T C COX5A Ensembl:ENSG00000178741 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1285652944 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112108,RMVar_hsa_circ_90015,RMVar_hsa_circ_173914,RMVar_hsa_circ_173915,RMVar_hsa_circ_95908,RMVar_hsa_circ_173920 39346 RMVar_ID_39346 Human_SNP_ID_735231976 A-to-I Human chrX - 150231505 150231505 150231505 CTCCAGAGCAGGTGGACAAGATGAAGGCTATCATTGAGAAGCTTCGCTTCACGTACAGAAGTGAC CTCCAGAGCAGGTGGACAAGATGAAGGCTATCGTTGAGAAGCTTCGCTTCACGTACAGAAGTGAC T C XRCC6P2 Ensembl:ENSG00000234825 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs782095608 Functional Loss SNV dbSNP153 33..33 33 - - - 39347 RMVar_ID_39347 Human_SNP_ID_735232088 A-to-I Human chrX - 150232154 150232154 150232154 CTAGAAGACCTGTTGCAGAAGGTTCACGCCAAAGAGACCAGGAAGCGAGCACTCAGCAGGTTAAA CTAGAAGACCTGTTGCAGAAGGTTCACGCCAAGGAGACCAGGAAGCGAGCACTCAGCAGGTTAAA T C XRCC6P2 Ensembl:ENSG00000234825 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs782692975 Functional Loss SNV dbSNP153 33..33 33 - - - 39348 RMVar_ID_39348 Human_SNP_ID_735232090 A-to-I Human chrX - 150232161 150232161 150232161 CAGCAAGCTAGAAGACCTGTTGCAGAAGGTTCACGCCAAAGAGACCAGGAAGCGAGCACTCAGCA CAGCAAGCTAGAAGACCTGTTGCAGAAGGTTCGCGCCAAAGAGACCAGGAAGCGAGCACTCAGCA T C XRCC6P2 Ensembl:ENSG00000234825 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs782054511 Functional Loss SNV dbSNP153 33..33 33 - - - 39349 RMVar_ID_39349 Human_SNP_ID_735232141 A-to-I Human chrX + 150232558 150232558 150232558 CTGCCCCTTAAACTGGTCAAGCTCTAGAATTCATTTTGCACCTGGATTATCCAGCTCCTATAAGA CTGCCCCTTAAACTGGTCAAGCTCTAGAATTCGTTTTGCACCTGGATTATCCAGCTCCTATAAGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879967949 Functional Loss SNV dbSNP153 33..33 33 - - - 39350 RMVar_ID_39350 Human_SNP_ID_735232143 A-to-I Human chrX + 150232585 150232585 150232585 AATTCATTTTGCACCTGGATTATCCAGCTCCTATAAGACATAAATATTTTTAAAATTCACTGAAT AATTCATTTTGCACCTGGATTATCCAGCTCCTGTAAGACATAAATATTTTTAAAATTCACTGAAT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879979875 Functional Loss SNV dbSNP153 33..33 33 - - - 39351 RMVar_ID_39351 Human_SNP_ID_735232144 A-to-I Human chrX + 150232592 150232592 150232592 TTTGCACCTGGATTATCCAGCTCCTATAAGACATAAATATTTTTAAAATTCACTGAATTTTTGTC TTTGCACCTGGATTATCCAGCTCCTATAAGACGTAAATATTTTTAAAATTCACTGAATTTTTGTC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs782532170 Functional Loss SNV dbSNP153 33..33 33 - - - 39352 RMVar_ID_39352 Human_SNP_ID_735232169 A-to-I Human chrX - 150232733 150232733 150232733 AAGGCTATGTTTGAATCTCCTAGTGAAGATGAATTGACACCTTTTGACATGAGCATCCAGTGTAT AAGGCTATGTTTGAATCTCCTAGTGAAGATGAGTTGACACCTTTTGACATGAGCATCCAGTGTAT T C XRCC6P2 Ensembl:ENSG00000234825 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs781989912 Functional Loss SNV dbSNP153 33..33 33 - - - 39353 RMVar_ID_39353 Human_SNP_ID_735366478 A-to-I Human chrX + 150993495 150993495 150993495 AAAGGGAGCTCTTTCCTTTCGCTGCTGCGACTACAGCCATGAGTATGCTCAGGCTTCAGAAGAGG AAAGGGAGCTCTTTCCTTTCGCTGCTGCGACTTCAGCCATGAGTATGCTCAGGCTTCAGAAGAGG A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1235270364 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5055541,Human_RBP_ID_27144961 39354 RMVar_ID_39354 Human_SNP_ID_735585590 A-to-I Human chrX - 152189847 152189847 152189847 GTGGCATATGCGACGGCCATGGACTGGTTCATAGCCGTCTGTTATGCCTTTGTATTTTCTGCACT GTGGCATATGCGACGGCCATGGACTGGTTCATGGCCGTCTGTTATGCCTTTGTATTTTCTGCACT T C GABRA3 Ensembl:ENSG00000011677 Protein coding CDS GSE56152 embryonic stem cells,wild type - 25708366 RNA-Seq:(High) rs2229939 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2242985,Human_Splice_Rec_2243003 RMVar_hsa_circ_264159,RMVar_hsa_circ_122101,RMVar_hsa_circ_108814,RMVar_hsa_circ_264161,RMVar_hsa_circ_315202,RMVar_hsa_circ_264158,RMVar_hsa_circ_310857,RMVar_hsa_circ_264160 39355 RMVar_ID_39355 Human_SNP_ID_735696634 A-to-I Human chrX - 152828571 152828571 152828571 TTCGTTCAAAAATCTGAAACGCGTGGCCAAGGAGTTGGGTGAGAACCTGACTGATGAGGAGCTGC TTCGTTCAAAAATCTGAAACGCGTGGCCAAGGGGTTGGGTGAGAACCTGACTGATGAGGAGCTGC T C CETN2 Ensembl:ENSG00000147400 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1321829537 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_968728,Human_RBP_ID_5055675,Human_RBP_ID_9409556,Human_RBP_ID_24334218 Human_Splice_Rec_2243276,Human_Splice_Rec_2243279 RMVar_hsa_circ_264170,RMVar_hsa_circ_118681,RMVar_hsa_circ_120465,RMVar_hsa_circ_90359,RMVar_hsa_circ_264171,RMVar_hsa_circ_264169 39356 RMVar_ID_39356 Human_SNP_ID_735734073 A-to-I Human chrX - 153032664 153032664 153032664 GGTATGGTGGTTGCACGCCTGTGGTCCCAGCTAGTCGGGAGGCTGAGGCGGGAGAATCGCTTGAG GGTATGGTGGTTGCACGCCTGTGGTCCCAGCTGGTCGGGAGGCTGAGGCGGGAGAATCGCTTGAG T C lnc-PNMA5-2 RNACentral:URS00008C090D lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1294439272 Functional Loss SNV dbSNP153 33..33 33 - - - 39357 RMVar_ID_39357 Human_SNP_ID_735804834 A-to-I Human chrX - 153461824 153461824 153461824 CACTCTGTGCTTAACTTTTCGAGGAGCCCCCAAACTGTTTTCCAGTGCGGCGGCACCATCTTCCT CACTCTGTGCTTAACTTTTCGAGGAGCCCCCAGACTGTTTTCCAGTGCGGCGGCACCATCTTCCT T C HAUS7,TREX2 Ensembl:ENSG00000213397,Ensembl:ENSG00000183479 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs782449841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16846060 RMVar_hsa_circ_77697,RMVar_hsa_circ_264187,RMVar_hsa_circ_50217 39358 RMVar_ID_39358 Human_SNP_ID_735813765 A-to-I Human chrX + 153505236 153505236 153505236 AAGTTCATGCTGGTGATGGGGGTGGGGCCCCTAGGTCTGAAGTCTGTGCCCAAAGAGATCTCCCC AAGTTCATGCTGGTGATGGGGGTGGGGCCCCTGGGTCTGAAGTCTGTGCCCAAAGAGATCTCCCC A G BGN Ensembl:ENSG00000182492 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs111898811 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47111,RMVar_hsa_circ_120269,RMVar_hsa_circ_126439,RMVar_hsa_circ_264188,RMVar_hsa_circ_49028,RMVar_hsa_circ_113944,RMVar_hsa_circ_264189 39359 RMVar_ID_39359 Human_SNP_ID_735813766 A-to-I Human chrX + 153505236 153505236 153505236 AAGTTCATGCTGGTGATGGGGGTGGGGCCCCTAGGTCTGAAGTCTGTGCCCAAAGAGATCTCCCC AAGTTCATGCTGGTGATGGGGGTGGGGCCCCTTGGTCTGAAGTCTGTGCCCAAAGAGATCTCCCC A T BGN Ensembl:ENSG00000182492 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs111898811 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47111,RMVar_hsa_circ_120269,RMVar_hsa_circ_126439,RMVar_hsa_circ_264188,RMVar_hsa_circ_49028,RMVar_hsa_circ_113944,RMVar_hsa_circ_264189 39360 RMVar_ID_39360 Human_SNP_ID_735867889 A-to-I Human chrX - 153759283 153759283 153759283 TTAATTTAATTTTTTTTTTTGAGACAGATCTCACTTTGTCACCCAGGCTGGAGTACAGTGGCGTG TTAATTTAATTTTTTTTTTTGAGACAGATCTCGCTTTGTCACCCAGGCTGGAGTACAGTGGCGTG T C U52111.1 Ensembl:ENSG00000232725 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1235714669 Functional Loss SNV dbSNP153 33..33 33 - - - 39361 RMVar_ID_39361 Human_SNP_ID_735867914 A-to-I Human chrX - 153759382 153759382 153759382 ATCATTGTAACCTCAAACTCCTGGTCTCAAGCAATTCTCCTGCCTCAGCCTCCTGGGTAGCTGGG ATCATTGTAACCTCAAACTCCTGGTCTCAAGCGATTCTCCTGCCTCAGCCTCCTGGGTAGCTGGG T C U52111.1 Ensembl:ENSG00000232725 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1557057547 Functional Loss SNV dbSNP153 33..33 33 - - - 39362 RMVar_ID_39362 Human_SNP_ID_735868252 A-to-I Human chrX - 153760916 153760916 153760916 GGAACTCCTGATCCACCTGCCTTGGCCTCCCAAAGTGCTAGGATTACAGGCGTGAGCCACTGTGC GGAACTCCTGATCCACCTGCCTTGGCCTCCCAGAGTGCTAGGATTACAGGCGTGAGCCACTGTGC T C U52111.1 Ensembl:ENSG00000232725 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1479216501 Functional Loss SNV dbSNP153 33..33 33 - - - 39363 RMVar_ID_39363 Human_SNP_ID_735868265 A-to-I Human chrX - 153760993 153760993 153760993 GGCACCCACCACCACGCCTGACTAATTTTTGTATCTTTACCAGACACAGGGTTTCACCATGTTGG GGCACCCACCACCACGCCTGACTAATTTTTGTGTCTTTACCAGACACAGGGTTTCACCATGTTGG T C U52111.1 Ensembl:ENSG00000232725 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256772047 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7986659 39364 RMVar_ID_39364 Human_SNP_ID_735919365 A-to-I Human chrX + 153977431 153977431 153977431 GAGGTCAGGAGTTCAATACCACCCCAGCCGATATGGCAAAATCCCATCTCTACTAAAATACAAAA GAGGTCAGGAGTTCAATACCACCCCAGCCGATGTGGCAAAATCCCATCTCTACTAAAATACAAAA A G TMEM187 Ensembl:ENSG00000177854 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs987646781 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96846,RMVar_hsa_circ_264269 39365 RMVar_ID_39365 Human_SNP_ID_735926892 A-to-I Human chrX - 154011115 154011115 154011115 GTATGACTGCACTCCAGCCTGGGTGACAGAGCAAGACCCTGTTTCAAAAAGAAAAACCCTGGGAA GTATGACTGCACTCCAGCCTGGGTGACAGAGCGAGACCCTGTTTCAAAAAGAAAAACCCTGGGAA T C IRAK1 Ensembl:ENSG00000184216 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs11556421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_731412,Human_RBP_ID_5056827,Human_RBP_ID_9244849,Human_RBP_ID_16847633,Human_RBP_ID_24334771,Human_RBP_ID_27163353 Human_Splice_Rec_2246908 Human_miRNA_ID_475585,Human_miRNA_ID_1266518,Human_miRNA_ID_2158304,Human_miRNA_ID_2611936,Human_miRNA_ID_2908992,Human_miRNA_ID_3027836 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 39366 RMVar_ID_39366 Human_SNP_ID_735926906 A-to-I Human chrX - 154011199 154011199 154011199 ACGCCTGTGGTCCCAGCTGCTGGGGAGGCTGAAGTAGGAGGATCATTTATGCTTGGGAGGTCGAG ACGCCTGTGGTCCCAGCTGCTGGGGAGGCTGACGTAGGAGGATCATTTATGCTTGGGAGGTCGAG T G IRAK1 Ensembl:ENSG00000184216 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1000137506 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_731415,Human_RBP_ID_2072013,Human_RBP_ID_3247347,Human_RBP_ID_7986944,Human_RBP_ID_16847641,Human_RBP_ID_18147777,Human_RBP_ID_18403758,Human_RBP_ID_18917230,Human_RBP_ID_24334772,Human_RBP_ID_26570231 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 39367 RMVar_ID_39367 Human_SNP_ID_735926930 A-to-I Human chrX - 154011363 154011363 154011363 AAGTGTGGCCGGGTGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGAGG AAGTGTGGCCGGGTGCGGTGGCTCACGCCTGTCATCCCAGCACTTTGGGAGGCCAAGGCAGGAGG T G IRAK1 Ensembl:ENSG00000184216 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1179901607 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23099614 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 39368 RMVar_ID_39368 Human_SNP_ID_735931413 A-to-I Human chrX - 154030432 154030430 154030432 AGGGAGAGCGCAAAGACATTGTTTCATCCTCCATGCCAAGGCCAAACAGAGAGGAGCCTGTGGAC AGGGAGAGCGCAAAGACATTGTTTCATCCTCC__GCCAAGGCCAAACAGAGAGGAGCCTGTGGAC CAT C MECP2 Ensembl:ENSG00000169057 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs267608630 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_731548,Human_RBP_ID_3977764,Human_RBP_ID_7987132,Human_RBP_ID_9340085 Human_miRNA_ID_1062714 39369 RMVar_ID_39369 Human_SNP_ID_735935141 A-to-I Human chrX - 154043219 154043219 154043219 CTGTGTCATTCCAGAACACTTTCAGCACCCAAAAGAAACCCCAGACACAGGAGCAGTCACCTCTT CTGTGTCATTCCAGAACACTTTCAGCACCCAACAGAAACCCCAGACACAGGAGCAGTCACCTCTT T G MECP2 Ensembl:ENSG00000169057 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1412674904 Functional Loss SNV dbSNP153 33..33 33 - - - 39370 RMVar_ID_39370 Human_SNP_ID_735938970 A-to-I Human chrX - 154065703 154065703 154065703 TAGCTCACTGCAGACTCGAACTCCTGGGCTCAAGTGGTCTTCCTGCCTCAGCCTCCTGCGTAGCT TAGCTCACTGCAGACTCGAACTCCTGGGCTCAGGTGGTCTTCCTGCCTCAGCCTCCTGCGTAGCT T C MECP2 Ensembl:ENSG00000169057 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1358901613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16848650 39371 RMVar_ID_39371 Human_SNP_ID_735939035 A-to-I Human chrX - 154066063 154066063 154066063 TCCATAGTCCCAGCTACTCGGGAAGCAGAGGCAGGAGGATTGCTTGATCCCAAGGAGGTCAAGGC TCCATAGTCCCAGCTACTCGGGAAGCAGAGGCGGGAGGATTGCTTGATCCCAAGGAGGTCAAGGC T C MECP2 Ensembl:ENSG00000169057 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs888059055 Functional Loss SNV dbSNP153 33..33 33 - - - 39372 RMVar_ID_39372 Human_SNP_ID_735939134 A-to-I Human chrX - 154066735 154066735 154066735 CAGCTCACTGCAACCTCTGCCTCCCGAGTTCAAGCGATTCCCATGCCTCAGCCTTCCAAGTAGCT CAGCTCACTGCAACCTCTGCCTCCCGAGTTCAGGCGATTCCCATGCCTCAGCCTTCCAAGTAGCT T C MECP2 Ensembl:ENSG00000169057 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs782691264 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16848662 39373 RMVar_ID_39373 Human_SNP_ID_735939659 A-to-I Human chrX - 154069791 154069791 154069791 CTCCATCACCCAGGCTGGAGTGCAGTGATGCAATCTCGGCTCACTGCAGTCTCTGCCTCCTGGAT CTCCATCACCCAGGCTGGAGTGCAGTGATGCAGTCTCGGCTCACTGCAGTCTCTGCCTCCTGGAT T C MECP2 Ensembl:ENSG00000169057 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs782266972 Functional Loss SNV dbSNP153 33..33 33 - - - 39374 RMVar_ID_39374 Human_SNP_ID_735939873 A-to-I Human chrX - 154070851 154070851 154070851 CGGCGCTCGCCTGTAGTCCCAGCTACTCAGGAAGCTGAGGTGGAGGGACTGCTTGAACCTAAGAG CGGCGCTCGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGTGGAGGGACTGCTTGAACCTAAGAG T C MECP2 Ensembl:ENSG00000169057 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388217864 Functional Loss SNV dbSNP153 33..33 33 - - - 39375 RMVar_ID_39375 Human_SNP_ID_735939874 A-to-I Human chrX - 154070855 154070855 154070855 ATGGCGGCGCTCGCCTGTAGTCCCAGCTACTCAGGAAGCTGAGGTGGAGGGACTGCTTGAACCTA ATGGCGGCGCTCGCCTGTAGTCCCAGCTACTCGGGAAGCTGAGGTGGAGGGACTGCTTGAACCTA T C MECP2 Ensembl:ENSG00000169057 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1192725387 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26264945 39376 RMVar_ID_39376 Human_SNP_ID_735939936 A-to-I Human chrX - 154071233 154071233 154071233 CACTGCAGCTTCAAATGCCTAGGCTTCAAACAATCCTCCTCCCTCAGCCTCCCGAGTAGCTAAGA CACTGCAGCTTCAAATGCCTAGGCTTCAAACAGTCCTCCTCCCTCAGCCTCCCGAGTAGCTAAGA T C MECP2 Ensembl:ENSG00000169057 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1483890410 Functional Loss SNV dbSNP153 33..33 33 - - - 39377 RMVar_ID_39377 Human_SNP_ID_735940197 A-to-I Human chrX - 154072857 154072857 154072857 GTGATCTGCCCGCCTCGGCCTCCCAAAGTTCTAGGATTATAGGCGTGAGCCACCATGCCCAGCCC GTGATCTGCCCGCCTCGGCCTCCCAAAGTTCTGGGATTATAGGCGTGAGCCACCATGCCCAGCCC T C MECP2 Ensembl:ENSG00000169057 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1013413865 Functional Loss SNV dbSNP153 33..33 33 - - - 39378 RMVar_ID_39378 Human_SNP_ID_735941959 A-to-I Human chrX - 154082527 154082527 154082527 GCATTTTCGGCCGGGTGTGGTGGCTCACGCCTATATTCCTAGCACTTTAGAAGGCCGAGGCGGGT GCATTTTCGGCCGGGTGTGGTGGCTCACGCCTGTATTCCTAGCACTTTAGAAGGCCGAGGCGGGT T C MECP2 Ensembl:ENSG00000169057 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1380726729 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26265016 39379 RMVar_ID_39379 Human_SNP_ID_735942233 A-to-I Human chrX - 154084152 154084152 154084152 ACGTCTTTCTCTGTCACCCAGGCTGGAGTGCAATGGCATGATCTCGGCTCACTGCAACCCCCACT ACGTCTTTCTCTGTCACCCAGGCTGGAGTGCAGTGGCATGATCTCGGCTCACTGCAACCCCCACT T C MECP2 Ensembl:ENSG00000169057 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs781879116 Functional Loss SNV dbSNP153 33..33 33 - - - 39380 RMVar_ID_39380 Human_SNP_ID_735943099 A-to-I Human chrX - 154088742 154088742 154088742 AATACATACAAAAGGGCCAGATGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAG AATACATACAAAAGGGCCAGATGCGGTGGCTCGTGCCTGTAATCCCAGCACTTTGGGAGGCTGAG T C MECP2 Ensembl:ENSG00000169057 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1443473960 Functional Loss SNV dbSNP153 33..33 33 - - - 39381 RMVar_ID_39381 Human_SNP_ID_735943313 A-to-I Human chrX - 154089749 154089749 154089749 CCAGGCTGGTGTCGAACTCCTGACCTCAGGCGATCCACCTGCCTTGGCCTCCCAAAGTGCTGGGA CCAGGCTGGTGTCGAACTCCTGACCTCAGGCGGTCCACCTGCCTTGGCCTCCCAAAGTGCTGGGA T C MECP2 Ensembl:ENSG00000169057 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs782199243 Functional Loss SNV dbSNP153 33..33 33 - - - 39382 RMVar_ID_39382 Human_SNP_ID_735974430 A-to-I Human chrX - 154351370 154351370 154351370 ACCACGTGGAGTTTTTCTCGTGTCTCAGGTCTAAAGGCTTTGAACAGAAGCCTGTGCCCCTTGAG ACCACGTGGAGTTTTTCTCGTGTCTCAGGTCTTAAGGCTTTGAACAGAAGCCTGTGCCCCTTGAG T A FLNA Ensembl:ENSG00000196924 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs113899441 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5411556,Human_RBP_ID_17580231 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 39383 RMVar_ID_39383 Human_SNP_ID_735974431 A-to-I Human chrX - 154351370 154351370 154351370 ACCACGTGGAGTTTTTCTCGTGTCTCAGGTCTAAAGGCTTTGAACAGAAGCCTGTGCCCCTTGAG ACCACGTGGAGTTTTTCTCGTGTCTCAGGTCTGAAGGCTTTGAACAGAAGCCTGTGCCCCTTGAG T C FLNA Ensembl:ENSG00000196924 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs113899441 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5411556,Human_RBP_ID_17580231 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 39384 RMVar_ID_39384 Human_SNP_ID_735974481 A-to-I Human chrX - 154351582 154351582 154351582 CGACGCCCGCCGCCTCACTGTTTCTAGCCTTCAGGTGAGGCACCGAGAGAAACCGCCCACCTGGG CGACGCCCGCCGCCTCACTGTTTCTAGCCTTCTGGTGAGGCACCGAGAGAAACCGCCCACCTGGG T A FLNA Ensembl:ENSG00000196924 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1137967 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19149797,Human_RBP_ID_24394848 Human_Splice_Rec_2247407,Human_Splice_Rec_2247497,Human_Splice_Rec_2247587,Human_Splice_Rec_2247680,Human_Splice_Rec_2247771,Human_Splice_Rec_2247855 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_79672,RMVar_hsa_circ_98864,RMVar_hsa_circ_264323,RMVar_hsa_circ_264324,RMVar_hsa_circ_264322,RMVar_hsa_circ_340695,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_264330,RMVar_hsa_circ_264327 39385 RMVar_ID_39385 Human_SNP_ID_735974482 A-to-I Human chrX - 154351582 154351582 154351582 CGACGCCCGCCGCCTCACTGTTTCTAGCCTTCAGGTGAGGCACCGAGAGAAACCGCCCACCTGGG CGACGCCCGCCGCCTCACTGTTTCTAGCCTTCGGGTGAGGCACCGAGAGAAACCGCCCACCTGGG T C FLNA Ensembl:ENSG00000196924 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1137967 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19149797,Human_RBP_ID_24394848 Human_Splice_Rec_2247407,Human_Splice_Rec_2247497,Human_Splice_Rec_2247587,Human_Splice_Rec_2247680,Human_Splice_Rec_2247771,Human_Splice_Rec_2247855 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_79672,RMVar_hsa_circ_98864,RMVar_hsa_circ_264323,RMVar_hsa_circ_264324,RMVar_hsa_circ_264322,RMVar_hsa_circ_340695,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_264330,RMVar_hsa_circ_264327 39386 RMVar_ID_39386 Human_SNP_ID_735983873 A-to-I Human chrX - 154395402 154395402 154395402 TTGCCCAGGCTGGAGTGCCATGGCACGATCTCAGCTCAGTGCAACCTCTGCCTCCCGGGTTCAAG TTGCCCAGGCTGGAGTGCCATGGCACGATCTCGGCTCAGTGCAACCTCTGCCTCCCGGGTTCAAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1197059102 Functional Loss SNV dbSNP153 33..33 33 - - - 39387 RMVar_ID_39387 Human_SNP_ID_735996935 A-to-I Human chrX + 154451717 154451678 154451717 TCTCCCAGGCTGGAGTGCAGTGGTGCAATCTCAGCTCGCTGCAGCCCCCACCTCCTGGGCTCAAG _________________________________GCTCGCTGCAGCCCCCACCTCCTGGGCTCAAG TGCTCTGTCTCCCAGGCTGGAGTGCAGTGGTGCAATCTCA T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1290718631 Functional Loss DEL dbSNP153 1..33 33 - - - 39388 RMVar_ID_39388 Human_SNP_ID_735996969 A-to-I Human chrX + 154451717 154451717 154451717 TCTCCCAGGCTGGAGTGCAGTGGTGCAATCTCAGCTCGCTGCAGCCCCCACCTCCTGGGCTCAAG TCTCCCAGGCTGGAGTGCAGTGGTGCAATCTCGGCTCGCTGCAGCCCCCACCTCCTGGGCTCAAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1261907864 Functional Loss SNV dbSNP153 33..33 33 - - - 39389 RMVar_ID_39389 Human_SNP_ID_736017052 A-to-I Human chrX - 154531677 154531677 154531677 TCTGTCCCAGAGCTTATTGGCCACTGGGTCTCACTCCTGAGTGGGGCCAGGGTGGGAGGGAGGGA TCTGTCCCAGAGCTTATTGGCCACTGGGTCTCTCTCCTGAGTGGGGCCAGGGTGGGAGGGAGGGA T A G6PD Ensembl:ENSG00000160211 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1003923823 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23217360,Human_RBP_ID_26574068 Human_miRNA_ID_2771548,Human_miRNA_ID_2771549 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_264556,RMVar_hsa_circ_264560,RMVar_hsa_circ_80187,RMVar_hsa_circ_90496,RMVar_hsa_circ_78607,RMVar_hsa_circ_264561,RMVar_hsa_circ_264558,RMVar_hsa_circ_264559,RMVar_hsa_circ_264557,RMVar_hsa_circ_264554,RMVar_hsa_circ_264555,RMVar_hsa_circ_264553 39390 RMVar_ID_39390 Human_SNP_ID_736017053 A-to-I Human chrX - 154531677 154531677 154531677 TCTGTCCCAGAGCTTATTGGCCACTGGGTCTCACTCCTGAGTGGGGCCAGGGTGGGAGGGAGGGA TCTGTCCCAGAGCTTATTGGCCACTGGGTCTCGCTCCTGAGTGGGGCCAGGGTGGGAGGGAGGGA T C G6PD Ensembl:ENSG00000160211 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1003923823 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23217360,Human_RBP_ID_26574068 Human_miRNA_ID_2771548,Human_miRNA_ID_2771549 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_264556,RMVar_hsa_circ_264560,RMVar_hsa_circ_80187,RMVar_hsa_circ_90496,RMVar_hsa_circ_78607,RMVar_hsa_circ_264561,RMVar_hsa_circ_264558,RMVar_hsa_circ_264559,RMVar_hsa_circ_264557,RMVar_hsa_circ_264554,RMVar_hsa_circ_264555,RMVar_hsa_circ_264553 39391 RMVar_ID_39391 Human_SNP_ID_736022348 A-to-I Human chrX + 154555449 154555449 154555449 TGGCATAAGGCCAGGCACAGTGGCCCATGCCTATAATCCCAGCACTTTCGGAGGCCGAGGTGGGA TGGCATAAGGCCAGGCACAGTGGCCCATGCCTGTAATCCCAGCACTTTCGGAGGCCGAGGTGGGA A G IKBKG Ensembl:ENSG00000269335 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1557235829 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_370380,RMVar_hsa_circ_264576 39392 RMVar_ID_39392 Human_SNP_ID_736074145 A-to-I Human chrX - 154919837 154919837 154919837 TGATGAAAGCATGGAACTGATTCTGCCTTCTGATGCCAGAGTGGGTCATCACTCCTTGATGAGAT TGATGAAAGCATGGAACTGATTCTGCCTTCTGTTGCCAGAGTGGGTCATCACTCCTTGATGAGAT T A F8,BX842559.2 Ensembl:ENSG00000185010,Ensembl:ENSG00000233688 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1164051415 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1818803,Human_miRNA_ID_1840538,Human_miRNA_ID_1886806,Human_miRNA_ID_1907822 RMVar_hsa_circ_108340,RMVar_hsa_circ_264605 39393 RMVar_ID_39393 Human_SNP_ID_736107717 A-to-I Human chrX + 155124971 155124971 155124971 AAAAAAAAAAAAGGTTAGCTGGGCATGGTGGCAGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTG AAAAAAAAAAAAGGTTAGCTGGGCATGGTGGCGGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTG A G lnc-BRCC3-2,lnc-BRCC3-2:2 RNACentral:URS00008BE0F8,RNACentral:URS00008B5FFB lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1192461317 Functional Loss SNV dbSNP153 33..33 33 - - - 39394 RMVar_ID_39394 Human_SNP_ID_736107723 A-to-I Human chrX + 155124981 155124981 155124981 AAGGTTAGCTGGGCATGGTGGCAGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGACGCAGGAGA AAGGTTAGCTGGGCATGGTGGCAGGCGCCTGTGGTCCCAGCTACTCGGGAGGCTGACGCAGGAGA A G lnc-BRCC3-2,lnc-BRCC3-2:2 RNACentral:URS00008BE0F8,RNACentral:URS00008B5FFB lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215361236 Functional Loss SNV dbSNP153 33..33 33 - - - 39395 RMVar_ID_39395 Human_SNP_ID_55520117 A-to-I Human chr1 - 240142856 240142856 240142856 GAGCTGAGGCCATTGCCAGTGTCTGTCCATGTAGGCCAGGCAGTGGATGTGGTGGGCCAGGCTGG GAGCTGAGGCCATTGCCAGTGTCTGTCCATGTGGGCCAGGCAGTGGATGTGGTGGGCCAGGCTGG T C AL359918.2 Ensembl:ENSG00000228818 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878996699 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8979555,Human_RBP_ID_17677184 Human_miRNA_ID_1900557 39396 RMVar_ID_39396 Human_SNP_ID_55520121 A-to-I Human chr1 - 240142860 240142860 240142860 TGAGGAGCTGAGGCCATTGCCAGTGTCTGTCCATGTAGGCCAGGCAGTGGATGTGGTGGGCCAGG TGAGGAGCTGAGGCCATTGCCAGTGTCTGTCCGTGTAGGCCAGGCAGTGGATGTGGTGGGCCAGG T C AL359918.2 Ensembl:ENSG00000228818 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878872243 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8979555,Human_RBP_ID_17677184 Human_miRNA_ID_1900557 39397 RMVar_ID_39397 Human_SNP_ID_55520293 A-to-I Human chr1 - 240143459 240143459 240143459 AGAAGGAAAAGAAGGACAAGGACAAAAAGGAAACCCCTGCTGACATGGGAGCACATCAGGGAGTG AGAAGGAAAAGAAGGACAAGGACAAAAAGGAAGCCCCTGCTGACATGGGAGCACATCAGGGAGTG T C AL359918.2 Ensembl:ENSG00000228818 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878884355 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1840561,Human_miRNA_ID_1841305,Human_miRNA_ID_1862797,Human_miRNA_ID_1908532 39398 RMVar_ID_39398 Human_SNP_ID_55520294 A-to-I Human chr1 - 240143466 240143466 240143466 AAAGGCAAGAAGGAAAAGAAGGACAAGGACAAAAAGGAAACCCCTGCTGACATGGGAGCACATCA AAAGGCAAGAAGGAAAAGAAGGACAAGGACAAGAAGGAAACCCCTGCTGACATGGGAGCACATCA T C AL359918.2 Ensembl:ENSG00000228818 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879153590 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1841305,Human_miRNA_ID_1844317,Human_miRNA_ID_1862797,Human_miRNA_ID_1908532 39399 RMVar_ID_39399 Human_SNP_ID_55520712 A-to-I Human chr1 - 240144912 240144912 240144912 TAGTAGGCTCCCAGAAGGAATTGGCATCATGGAGTCATGAGTATATCAGGCACCTGGCAGGAGAA TAGTAGGCTCCCAGAAGGAATTGGCATCATGGGGTCATGAGTATATCAGGCACCTGGCAGGAGAA T C AL359918.2 Ensembl:ENSG00000228818 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1558318564 Functional Loss SNV dbSNP153 33..33 33 - - - 39400 RMVar_ID_39400 Human_SNP_ID_55540286 A-to-I Human chr1 + 240214981 240214981 240214981 CCAGCTACTTGGGAAGCTGAGATGGGAAGATCATCTGAGCCCAGGGAGGTTGAGGCTGCAGTGAG CCAGCTACTTGGGAAGCTGAGATGGGAAGATCTTCTGAGCCCAGGGAGGTTGAGGCTGCAGTGAG A T FMN2 Ensembl:ENSG00000155816 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1376220385 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24665312 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_141040 39401 RMVar_ID_39401 Human_SNP_ID_55581167 A-to-I Human chr1 + 240379937 240379937 240379937 AACACAATTCATCAGGTCAACAGGATTTCACTATCCAAAATATATATGCACCCAATAGCAGAGCA AACACAATTCATCAGGTCAACAGGATTTCACTGTCCAAAATATATATGCACCCAATAGCAGAGCA A G FMN2 Ensembl:ENSG00000155816 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1199245073 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113588,RMVar_hsa_circ_141034,RMVar_hsa_circ_47648,RMVar_hsa_circ_283079,RMVar_hsa_circ_300441,RMVar_hsa_circ_4120,RMVar_hsa_circ_141049,RMVar_hsa_circ_141046,RMVar_hsa_circ_141047,RMVar_hsa_circ_302254,RMVar_hsa_circ_292002,RMVar_hsa_circ_335480,RMVar_hsa_circ_141048,RMVar_hsa_circ_340901,RMVar_hsa_circ_7284,RMVar_hsa_circ_141059,RMVar_hsa_circ_348974,RMVar_hsa_circ_141057,RMVar_hsa_circ_333144,RMVar_hsa_circ_26511,RMVar_hsa_circ_300585,RMVar_hsa_circ_141058 39402 RMVar_ID_39402 Human_SNP_ID_55585421 A-to-I Human chr1 + 240397683 240397683 240397683 GTGGTGGTAGGGGCCTGTAATCCCAGCTATTCAGAAGGCTGAGGCATGAGAATCGCTTGAACCTG GTGGTGGTAGGGGCCTGTAATCCCAGCTATTCGGAAGGCTGAGGCATGAGAATCGCTTGAACCTG A G FMN2 Ensembl:ENSG00000155816 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs566997992 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24665835 RMVar_hsa_circ_113588,RMVar_hsa_circ_141034,RMVar_hsa_circ_283079,RMVar_hsa_circ_141047,RMVar_hsa_circ_292002,RMVar_hsa_circ_141048,RMVar_hsa_circ_340901,RMVar_hsa_circ_7284,RMVar_hsa_circ_141059,RMVar_hsa_circ_300585,RMVar_hsa_circ_141060,RMVar_hsa_circ_141061,RMVar_hsa_circ_323522 39403 RMVar_ID_39403 Human_SNP_ID_55585447 A-to-I Human chr1 + 240397747 240397747 240397747 GGGAGGCGGAGGTTGCAGTGAGCCAAGATCGCACTGCTGCACTCCAGCCCAGGCAACATAGACTC GGGAGGCGGAGGTTGCAGTGAGCCAAGATCGCGCTGCTGCACTCCAGCCCAGGCAACATAGACTC A G FMN2 Ensembl:ENSG00000155816 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1366505326 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113588,RMVar_hsa_circ_141034,RMVar_hsa_circ_283079,RMVar_hsa_circ_141047,RMVar_hsa_circ_292002,RMVar_hsa_circ_141048,RMVar_hsa_circ_340901,RMVar_hsa_circ_7284,RMVar_hsa_circ_141059,RMVar_hsa_circ_300585,RMVar_hsa_circ_141060,RMVar_hsa_circ_141061,RMVar_hsa_circ_323522 39404 RMVar_ID_39404 Human_SNP_ID_55796250 A-to-I Human chr1 - 241250952 241250951 241250952 CTGAGCACCAATGCTAAGTGTTAGGGATTTAAAGATGAGCAAGGCATAGTCCCTACTTTTTAAAT CTGAGCACCAATGCTAAGTGTTAGGGATTTAA_GATGAGCAAGGCATAGTCCCTACTTTTTAAAT CT C RGS7 Ensembl:ENSG00000182901 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs998732214 Functional Loss DEL dbSNP153 33..33 33 - - - 39405 RMVar_ID_39405 Human_SNP_ID_55805224 A-to-I Human chr1 - 241288629 241288629 241288629 GTGGCCTCCCTTACTTTTGCTTCCAGACAGATAACCGTGGGCTCTGCAGCAAAGCACCTTTTTCC GTGGCCTCCCTTACTTTTGCTTCCAGACAGATGACCGTGGGCTCTGCAGCAAAGCACCTTTTTCC T C RGS7 Ensembl:ENSG00000182901 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1236959326 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18568559 39406 RMVar_ID_39406 Human_SNP_ID_55942749 A-to-I Human chr1 + 241852497 241852497 241852497 GTAGTCTATATGATACCAATTTTTAAAATTTTAAGCCAGGCTCAGTGGCTTGCACCTGTTGTCCT GTAGTCTATATGATACCAATTTTTAAAATTTTGAGCCAGGCTCAGTGGCTTGCACCTGTTGTCCT A G EXO1 Ensembl:ENSG00000174371 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1278468626 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10869060 RMVar_hsa_circ_8732,RMVar_hsa_circ_141087,RMVar_hsa_circ_95280,RMVar_hsa_circ_319826,RMVar_hsa_circ_365720,RMVar_hsa_circ_51137,RMVar_hsa_circ_28176,RMVar_hsa_circ_141088 39407 RMVar_ID_39407 Human_SNP_ID_55960838 A-to-I Human chr1 + 241920162 241920162 241920162 ACTGGAGTGCAGTGGCGTGATCACGATTAACTACAACCTCAGCTTCCTGAGCTCAGGTGATTCTC ACTGGAGTGCAGTGGCGTGATCACGATTAACTGCAACCTCAGCTTCCTGAGCTCAGGTGATTCTC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1452156585 Functional Loss SNV dbSNP153 33..33 33 - - - 39408 RMVar_ID_39408 Human_SNP_ID_56263585 A-to-I Human chr1 - 243124812 243124811 243124812 CCCATTCTGTCTAATAAAGGAAGACTGAAAAAAGGTTTTAAAGAACATAAATGGAAAGATACAAA CCCATTCTGTCTAATAAAGGAAGACTGAAAAA_GGTTTTAAAGAACATAAATGGAAAGATACAAA CT C CEP170 Ensembl:ENSG00000143702 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1044988019 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_113260,RMVar_hsa_circ_141115 39409 RMVar_ID_39409 Human_SNP_ID_56290325 A-to-I Human chr1 - 243243025 243243025 243243025 TAACAAATTCCAGAATGTTAAGGATCTGCTATAGAGAATCAACAATTCAAAAATTTAGGACCGGG TAACAAATTCCAGAATGTTAAGGATCTGCTATGGAGAATCAACAATTCAAAAATTTAGGACCGGG T C CEP170 Ensembl:ENSG00000143702 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1295452082 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10873204 RMVar_hsa_circ_84463,RMVar_hsa_circ_141132 39410 RMVar_ID_39410 Human_SNP_ID_56290992 A-to-I Human chr1 - 243245407 243245407 243245407 TGGCCAAGGTTTTTTATTTTTTTATAGAGACAAGGTCTCATTTTGTTCCCTAGGCTGGTCTCAAA TGGCCAAGGTTTTTTATTTTTTTATAGAGACAGGGTCTCATTTTGTTCCCTAGGCTGGTCTCAAA T C CEP170 Ensembl:ENSG00000143702 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1304785328 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10873246 RMVar_hsa_circ_84463,RMVar_hsa_circ_141132 39411 RMVar_ID_39411 Human_SNP_ID_56377138 A-to-I Human chr1 - 243609575 243609575 243609575 CGGCTCACTGCAACTTCTGCCTCCTGGGCTCAAGCAGTCCTCATGCCTCAGTCTCCCGAGTAGCT CGGCTCACTGCAACTTCTGCCTCCTGGGCTCAGGCAGTCCTCATGCCTCAGTCTCCCGAGTAGCT T C AKT3 Ensembl:ENSG00000117020 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs951325608 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1453,RMVar_hsa_circ_11758,RMVar_hsa_circ_295918,RMVar_hsa_circ_340959,RMVar_hsa_circ_276750,RMVar_hsa_circ_280715,RMVar_hsa_circ_304223,RMVar_hsa_circ_323199,RMVar_hsa_circ_331738,RMVar_hsa_circ_311497,RMVar_hsa_circ_269994,RMVar_hsa_circ_141182,RMVar_hsa_circ_141183,RMVar_hsa_circ_141184,RMVar_hsa_circ_47034,RMVar_hsa_circ_270555,RMVar_hsa_circ_119535,RMVar_hsa_circ_141186,RMVar_hsa_circ_141185,RMVar_hsa_circ_141192,RMVar_hsa_circ_280795,RMVar_hsa_circ_302399,RMVar_hsa_circ_341272,RMVar_hsa_circ_316165,RMVar_hsa_circ_291106,RMVar_hsa_circ_141194,RMVar_hsa_circ_271040,RMVar_hsa_circ_141193,RMVar_hsa_circ_141190,RMVar_hsa_circ_141191,RMVar_hsa_circ_307063,RMVar_hsa_circ_328843,RMVar_hsa_circ_314450,RMVar_hsa_circ_302648,RMVar_hsa_circ_141195,RMVar_hsa_circ_141197,RMVar_hsa_circ_141199,RMVar_hsa_circ_141200,RMVar_hsa_circ_141198,RMVar_hsa_circ_141196 39412 RMVar_ID_39412 Human_SNP_ID_56377820 A-to-I Human chr1 - 243612396 243612396 243612396 ACTTCATTCATTCAGGGCTTGCATGGTGGCTCAGACTTGTAATCCCAGCAGTTGGGGAGGCTGAG ACTTCATTCATTCAGGGCTTGCATGGTGGCTCGGACTTGTAATCCCAGCAGTTGGGGAGGCTGAG T C AKT3 Ensembl:ENSG00000117020 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs988278963 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1453,RMVar_hsa_circ_11758,RMVar_hsa_circ_295918,RMVar_hsa_circ_340959,RMVar_hsa_circ_276750,RMVar_hsa_circ_280715,RMVar_hsa_circ_304223,RMVar_hsa_circ_323199,RMVar_hsa_circ_331738,RMVar_hsa_circ_311497,RMVar_hsa_circ_269994,RMVar_hsa_circ_141182,RMVar_hsa_circ_141183,RMVar_hsa_circ_141184,RMVar_hsa_circ_47034,RMVar_hsa_circ_270555,RMVar_hsa_circ_119535,RMVar_hsa_circ_141186,RMVar_hsa_circ_141185,RMVar_hsa_circ_141192,RMVar_hsa_circ_280795,RMVar_hsa_circ_302399,RMVar_hsa_circ_341272,RMVar_hsa_circ_316165,RMVar_hsa_circ_291106,RMVar_hsa_circ_141194,RMVar_hsa_circ_271040,RMVar_hsa_circ_141193,RMVar_hsa_circ_141190,RMVar_hsa_circ_141191,RMVar_hsa_circ_307063,RMVar_hsa_circ_328843,RMVar_hsa_circ_314450,RMVar_hsa_circ_302648,RMVar_hsa_circ_141195,RMVar_hsa_circ_141197,RMVar_hsa_circ_141199,RMVar_hsa_circ_141200,RMVar_hsa_circ_141198,RMVar_hsa_circ_141196 39413 RMVar_ID_39413 Human_SNP_ID_56377929 A-to-I Human chr1 - 243612876 243612876 243612876 CACCGCCACACCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGA CACCGCCACACCCAGCTAATTTTTGTATTTTTGGTAGAGATGGGGTTTCACCATGTTGGCCAGGA T C AKT3 Ensembl:ENSG00000117020 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1029822113 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1453,RMVar_hsa_circ_11758,RMVar_hsa_circ_295918,RMVar_hsa_circ_340959,RMVar_hsa_circ_276750,RMVar_hsa_circ_280715,RMVar_hsa_circ_304223,RMVar_hsa_circ_323199,RMVar_hsa_circ_331738,RMVar_hsa_circ_311497,RMVar_hsa_circ_269994,RMVar_hsa_circ_141182,RMVar_hsa_circ_141183,RMVar_hsa_circ_141184,RMVar_hsa_circ_47034,RMVar_hsa_circ_270555,RMVar_hsa_circ_119535,RMVar_hsa_circ_141186,RMVar_hsa_circ_141185,RMVar_hsa_circ_141192,RMVar_hsa_circ_280795,RMVar_hsa_circ_302399,RMVar_hsa_circ_341272,RMVar_hsa_circ_316165,RMVar_hsa_circ_291106,RMVar_hsa_circ_141194,RMVar_hsa_circ_271040,RMVar_hsa_circ_141193,RMVar_hsa_circ_141190,RMVar_hsa_circ_141191,RMVar_hsa_circ_307063,RMVar_hsa_circ_328843,RMVar_hsa_circ_314450,RMVar_hsa_circ_302648,RMVar_hsa_circ_141195,RMVar_hsa_circ_141197,RMVar_hsa_circ_141199,RMVar_hsa_circ_141200,RMVar_hsa_circ_141198,RMVar_hsa_circ_141196 39414 RMVar_ID_39414 Human_SNP_ID_56407514 A-to-I Human chr1 - 243727469 243727469 243727469 CTAGACCTTCCTGGGCAACATAGCAAGACCCTATCTCCACAAAAAGTGAACAAAATTAGCCACGC CTAGACCTTCCTGGGCAACATAGCAAGACCCTGTCTCCACAAAAAGTGAACAAAATTAGCCACGC T C AL662889.1,AKT3 Ensembl:ENSG00000232184,Ensembl:ENSG00000117020 lincRNA,Protein coding intron,intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs943343790 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_276750,RMVar_hsa_circ_269994,RMVar_hsa_circ_141184,RMVar_hsa_circ_270555,RMVar_hsa_circ_141194,RMVar_hsa_circ_271040,RMVar_hsa_circ_307063,RMVar_hsa_circ_141195,RMVar_hsa_circ_271937,RMVar_hsa_circ_141207,RMVar_hsa_circ_5181,RMVar_hsa_circ_272058,RMVar_hsa_circ_141210,RMVar_hsa_circ_304502,RMVar_hsa_circ_141216,RMVar_hsa_circ_274361,RMVar_hsa_circ_141218,RMVar_hsa_circ_299777,RMVar_hsa_circ_337957,RMVar_hsa_circ_141223,RMVar_hsa_circ_141224,RMVar_hsa_circ_141222 39415 RMVar_ID_39415 Human_SNP_ID_56413825 A-to-I Human chr1 - 243754654 243754654 243754654 GCAACCTAGATCCCTCGCATGCACAGTTCACAATAGGGTTCGCACTCCTGTGAGAATCTGTTGCC GCAACCTAGATCCCTCGCATGCACAGTTCACAGTAGGGTTCGCACTCCTGTGAGAATCTGTTGCC T C AKT3 Ensembl:ENSG00000117020 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1285831398 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_276750,RMVar_hsa_circ_269994,RMVar_hsa_circ_141184,RMVar_hsa_circ_270555,RMVar_hsa_circ_141194,RMVar_hsa_circ_271040,RMVar_hsa_circ_307063,RMVar_hsa_circ_141195,RMVar_hsa_circ_271937,RMVar_hsa_circ_141207,RMVar_hsa_circ_5181,RMVar_hsa_circ_272058,RMVar_hsa_circ_141210,RMVar_hsa_circ_304502,RMVar_hsa_circ_141216,RMVar_hsa_circ_274361,RMVar_hsa_circ_299777,RMVar_hsa_circ_141224 39416 RMVar_ID_39416 Human_SNP_ID_56417524 A-to-I Human chr1 - 243770022 243770022 243770022 GAAATGATGATGGGACAACCCGATTTCCACATATAAAAGAATGAATTTGGACTCCTTACCTCACA GAAATGATGATGGGACAACCCGATTTCCACATGTAAAAGAATGAATTTGGACTCCTTACCTCACA T C AKT3 Ensembl:ENSG00000117020 Protein coding intron GSE107867 ASD brains,cerebellum;ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1208712518 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24670277 RMVar_hsa_circ_276750,RMVar_hsa_circ_269994,RMVar_hsa_circ_141184,RMVar_hsa_circ_270555,RMVar_hsa_circ_141194,RMVar_hsa_circ_271040,RMVar_hsa_circ_307063,RMVar_hsa_circ_141195,RMVar_hsa_circ_271937,RMVar_hsa_circ_141207,RMVar_hsa_circ_5181,RMVar_hsa_circ_272058,RMVar_hsa_circ_141210,RMVar_hsa_circ_304502,RMVar_hsa_circ_141216,RMVar_hsa_circ_274361,RMVar_hsa_circ_299777,RMVar_hsa_circ_141224 39417 RMVar_ID_39417 Human_SNP_ID_56424675 A-to-I Human chr1 - 243798374 243798374 243798374 AAAAAAAAAAAAATTAAAAATTAGCCAGGTGTAGTGGTGCATGCCTGTAGTCCCAGCTATGTGGG AAAAAAAAAAAAATTAAAAATTAGCCAGGTGTGGTGGTGCATGCCTGTAGTCCCAGCTATGTGGG T C AKT3 Ensembl:ENSG00000117020 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1316046405 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_276750,RMVar_hsa_circ_269994,RMVar_hsa_circ_141184,RMVar_hsa_circ_270555,RMVar_hsa_circ_141194,RMVar_hsa_circ_271040,RMVar_hsa_circ_307063,RMVar_hsa_circ_141195,RMVar_hsa_circ_271937,RMVar_hsa_circ_141207,RMVar_hsa_circ_5181,RMVar_hsa_circ_272058,RMVar_hsa_circ_141210,RMVar_hsa_circ_304502,RMVar_hsa_circ_141216,RMVar_hsa_circ_274361,RMVar_hsa_circ_299777,RMVar_hsa_circ_141224 39418 RMVar_ID_39418 Human_SNP_ID_56555036 A-to-I Human chr1 - 244310033 244310033 244310033 TTTTGTAGAGACGAGGTTTCACCATGTTGTCCAGGTTGGTCTCAAACTCCTGGGCTCAAGCAATC TTTTGTAGAGACGAGGTTTCACCATGTTGTCCGGGTTGGTCTCAAACTCCTGGGCTCAAGCAATC T C lnc-ADSS-4,lnc-ADSS-4:2 RNACentral:URS00009B8986,RNACentral:URS00008B6F0E lincRNA,lincRNA exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1218149795 Functional Loss SNV dbSNP153 33..33 33 - - - 39419 RMVar_ID_39419 Human_SNP_ID_56584265 A-to-I Human chr1 - 244420958 244420958 244420958 ATGGTTGGCCAAACACAGTGGCTTACACCTGTAATTCAGCACTTTGGAGGCTGAGGTGGGAGGAT ATGGTTGGCCAAACACAGTGGCTTACACCTGTGATTCAGCACTTTGGAGGCTGAGGTGGGAGGAT T C ADSS2 Ensembl:ENSG00000035687 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1033670291 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24671653 RMVar_hsa_circ_107805,RMVar_hsa_circ_110404,RMVar_hsa_circ_99366,RMVar_hsa_circ_6698,RMVar_hsa_circ_141234,RMVar_hsa_circ_141235,RMVar_hsa_circ_141243,RMVar_hsa_circ_141240,RMVar_hsa_circ_378231,RMVar_hsa_circ_141233,RMVar_hsa_circ_141241,RMVar_hsa_circ_72649,RMVar_hsa_circ_141242,RMVar_hsa_circ_354455,RMVar_hsa_circ_335596,RMVar_hsa_circ_51124,RMVar_hsa_circ_294661,RMVar_hsa_circ_359608,RMVar_hsa_circ_14360,RMVar_hsa_circ_75066,RMVar_hsa_circ_353935,RMVar_hsa_circ_141245,RMVar_hsa_circ_281981,RMVar_hsa_circ_288949,RMVar_hsa_circ_141247 39420 RMVar_ID_39420 Human_SNP_ID_56584499 A-to-I Human chr1 - 244421995 244421995 244421995 CCATTTTCTTTTTATTCAGCTATGCAATAAATATTTTATTTTATTTTATTTTTTGAGACAGGGTC CCATTTTCTTTTTATTCAGCTATGCAATAAATCTTTTATTTTATTTTATTTTTTGAGACAGGGTC T G ADSS2 Ensembl:ENSG00000035687 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs745758216 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5795610 RMVar_hsa_circ_107805,RMVar_hsa_circ_110404,RMVar_hsa_circ_99366,RMVar_hsa_circ_6698,RMVar_hsa_circ_141234,RMVar_hsa_circ_141235,RMVar_hsa_circ_141243,RMVar_hsa_circ_141240,RMVar_hsa_circ_378231,RMVar_hsa_circ_141233,RMVar_hsa_circ_141241,RMVar_hsa_circ_72649,RMVar_hsa_circ_141242,RMVar_hsa_circ_354455,RMVar_hsa_circ_335596,RMVar_hsa_circ_51124,RMVar_hsa_circ_294661,RMVar_hsa_circ_359608,RMVar_hsa_circ_14360,RMVar_hsa_circ_75066,RMVar_hsa_circ_353935,RMVar_hsa_circ_141245,RMVar_hsa_circ_281981,RMVar_hsa_circ_288949,RMVar_hsa_circ_141247 39421 RMVar_ID_39421 Human_SNP_ID_56587059 A-to-I Human chr1 - 244433074 244433074 244433074 CCACCACCACACCCAGCTAATTTCGTATTTTTAGTAGAGACGGGGTTTTACCATGTTGACCAGGC CCACCACCACACCCAGCTAATTTCGTATTTTTGGTAGAGACGGGGTTTTACCATGTTGACCAGGC T C ADSS2 Ensembl:ENSG00000035687 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1051975410 Functional Loss SNV dbSNP153 33..33 33 - - - 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 39422 RMVar_ID_39422 Human_SNP_ID_56587102 A-to-I Human chr1 - 244433227 244433227 244433227 TAGAGATTGTGTTTCCTTTTTTGTGAGACAGCATCTCGCTCCGCCACATACACTGGAGTGTAGTG TAGAGATTGTGTTTCCTTTTTTGTGAGACAGCGTCTCGCTCCGCCACATACACTGGAGTGTAGTG T C ADSS2 Ensembl:ENSG00000035687 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1479469920 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3306763 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 39423 RMVar_ID_39423 Human_SNP_ID_56589209 A-to-I Human chr1 - 244441159 244441159 244441159 AGCTACTTGGGGGACTGAGGCAGGAGAATGGCATGAACCCGAGAGGCGGAGTTTGCAGTGGGCCG AGCTACTTGGGGGACTGAGGCAGGAGAATGGCGTGAACCCGAGAGGCGGAGTTTGCAGTGGGCCG T C ADSS2 Ensembl:ENSG00000035687 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs866348013 Functional Loss SNV dbSNP153 33..33 33 - - - 39424 RMVar_ID_39424 Human_SNP_ID_56589219 A-to-I Human chr1 - 244441187 244441187 244441187 GGGCATGGCGGCAGGCGCCTGTAGTCCCAGCTACTTGGGGGACTGAGGCAGGAGAATGGCATGAA GGGCATGGCGGCAGGCGCCTGTAGTCCCAGCTGCTTGGGGGACTGAGGCAGGAGAATGGCATGAA T C ADSS2 Ensembl:ENSG00000035687 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs998616473 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_100051 39425 RMVar_ID_39425 Human_SNP_ID_56589422 A-to-I Human chr1 - 244441821 244441821 244441821 CTCCCGAGTAGCTGGGACTACAGGCACGTGCCACCACGCCTGGCTAATTTTTTGTATTTTTAGTA CTCCCGAGTAGCTGGGACTACAGGCACGTGCCGCCACGCCTGGCTAATTTTTTGTATTTTTAGTA T C ADSS2 Ensembl:ENSG00000035687 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs367557373 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_100053 39426 RMVar_ID_39426 Human_SNP_ID_56644188 A-to-I Human chr1 + 244669417 244669417 244669417 AGAAACTAGACTGGCCAGTTGCTCTGGCTCACACCTGTAATCTCAGCACTTTGGGAGGCCGAGGT AGAAACTAGACTGGCCAGTTGCTCTGGCTCACTCCTGTAATCTCAGCACTTTGGGAGGCCGAGGT A T DESI2 Ensembl:ENSG00000121644 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs988023138 Functional Loss SNV dbSNP153 33..33 33 - - - 39427 RMVar_ID_39427 Human_SNP_ID_56650525 A-to-I Human chr1 + 244695873 244695873 244695873 TCATAGTTCATTGCAGCTGGGAACTCAGGCTCAAGTGAGCCTCCTGCCTCAGCCTCCCAAGTAGC TCATAGTTCATTGCAGCTGGGAACTCAGGCTCCAGTGAGCCTCCTGCCTCAGCCTCCCAAGTAGC A C DESI2 Ensembl:ENSG00000121644 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1332820352 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_141257,RMVar_hsa_circ_141256,RMVar_hsa_circ_87542,RMVar_hsa_circ_85081 39428 RMVar_ID_39428 Human_SNP_ID_56653175 A-to-I Human chr1 + 244704932 244704932 244704932 CACCGGCCTCAGCCTCCCAAAGTGCTGGTATTACAGGTGTGAGCCACCGCGCCTGGCCCACACTT CACCGGCCTCAGCCTCCCAAAGTGCTGGTATTCCAGGTGTGAGCCACCGCGCCTGGCCCACACTT A C DESI2 Ensembl:ENSG00000121644 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs943918355 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_141257,RMVar_hsa_circ_141256,RMVar_hsa_circ_87542,RMVar_hsa_circ_85081 39429 RMVar_ID_39429 Human_SNP_ID_56685472 A-to-I Human chr1 - 244828932 244828932 244828932 TATTTTTAGTCCAGATGGGGTTTCACCACGTTAGTCAAGCTGGTGTCGAACTCCTGACCTCAGGC TATTTTTAGTCCAGATGGGGTTTCACCACGTTTGTCAAGCTGGTGTCGAACTCCTGACCTCAGGC T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1246559995 Functional Loss SNV dbSNP153 33..33 33 - - - 39430 RMVar_ID_39430 Human_SNP_ID_56690414 A-to-I Human chr1 + 244844651 244844651 244844651 GTGGTGGTGCATGCCTGTAGTCCCAGGTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCCG GTGGTGGTGCATGCCTGTAGTCCCAGGTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCCG A G COX20 Ensembl:ENSG00000203667 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1324423306 Functional Loss SNV dbSNP153 33..33 33 - - - 39431 RMVar_ID_39431 Human_SNP_ID_56690774 A-to-I Human chr1 - 244845742 244845742 244845742 AAATTAGCCAGACGTGGTGGCACGCACCTGCAATCCCAGCTACTTGGGGGGCTGAGGCAGGAGAA AAATTAGCCAGACGTGGTGGCACGCACCTGCAGTCCCAGCTACTTGGGGGGCTGAGGCAGGAGAA T C HNRNPU Ensembl:ENSG00000153187 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1012880228 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69264,RMVar_hsa_circ_328999,RMVar_hsa_circ_344063,RMVar_hsa_circ_368750,RMVar_hsa_circ_71175,RMVar_hsa_circ_289315,RMVar_hsa_circ_70811,RMVar_hsa_circ_19731,RMVar_hsa_circ_19963,RMVar_hsa_circ_141260,RMVar_hsa_circ_141261 39432 RMVar_ID_39432 Human_SNP_ID_56724496 A-to-I Human chr1 - 244967902 244967902 244967902 AAAATAGAAAAATTAGCCGAATGTGGTGGCTCACGCCTGTAATCCCAGCTACTCGGGAGGCTGAG AAAATAGAAAAATTAGCCGAATGTGGTGGCTCCCGCCTGTAATCCCAGCTACTCGGGAGGCTGAG T G LOC101928068 RNACentral:URS000075AA18 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1241573589 Functional Loss SNV dbSNP153 33..33 33 - - - 39433 RMVar_ID_39433 Human_SNP_ID_56724505 A-to-I Human chr1 - 244967929 244967929 244967929 CAACATGGTAAAACCCCATCTCTACTAAAAATAGAAAAATTAGCCGAATGTGGTGGCTCACGCCT CAACATGGTAAAACCCCATCTCTACTAAAAATTGAAAAATTAGCCGAATGTGGTGGCTCACGCCT T A LOC101928068 RNACentral:URS000075AA18 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1386978185 Functional Loss SNV dbSNP153 33..33 33 - - - 39434 RMVar_ID_39434 Human_SNP_ID_56726819 A-to-I Human chr1 + 244974674 244974673 244974674 AAATAACGTCTTTGTTTTTTTTTTCTTCTTTTATTTTGAGACAGGGTCTTGCTCTGCTGCCCAGG AAATAACGTCTTTGTTTTTTTTTTCTTCTTTT_TTTTGAGACAGGGTCTTGCTCTGCTGCCCAGG TA T EFCAB2 Ensembl:ENSG00000203666 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1558223485 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_5797536 39435 RMVar_ID_39435 Human_SNP_ID_56726820 A-to-I Human chr1 + 244974674 244974674 244974674 AAATAACGTCTTTGTTTTTTTTTTCTTCTTTTATTTTGAGACAGGGTCTTGCTCTGCTGCCCAGG AAATAACGTCTTTGTTTTTTTTTTCTTCTTTTTTTTTGAGACAGGGTCTTGCTCTGCTGCCCAGG A T EFCAB2 Ensembl:ENSG00000203666 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1194971978 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5797536 39436 RMVar_ID_39436 Human_SNP_ID_56728087 A-to-I Human chr1 + 244979447 244979447 244979447 TATGTCTCAGCCTCCCAAGTAGCTGGGATTACAGACATGTGCCACCATGCTGGGCTCATTTTTTT TATGTCTCAGCCTCCCAAGTAGCTGGGATTACGGACATGTGCCACCATGCTGGGCTCATTTTTTT A G EFCAB2 Ensembl:ENSG00000203666 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs778098461 Functional Loss SNV dbSNP153 33..33 33 - - - 39437 RMVar_ID_39437 Human_SNP_ID_56729920 A-to-I Human chr1 + 244986659 244986659 244986659 GGGAGGCTGAGGTGGGAGGATTGCTTGAGCCTAGAAGTTCGAGGATGCAGTGAGCTATGATCACA GGGAGGCTGAGGTGGGAGGATTGCTTGAGCCTGGAAGTTCGAGGATGCAGTGAGCTATGATCACA A G EFCAB2 Ensembl:ENSG00000203666 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041874521 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_103334 39438 RMVar_ID_39438 Human_SNP_ID_56734638 A-to-I Human chr1 + 245006787 245006787 245006787 AAAAACCTGTCTCTACTAAAAACACAAAAATTAGCTGGGCATGGTGGCACAGGCCTGCAGTCCTA AAAAACCTGTCTCTACTAAAAACACAAAAATTTGCTGGGCATGGTGGCACAGGCCTGCAGTCCTA A T EFCAB2 Ensembl:ENSG00000203666 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1028684003 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_141277,RMVar_hsa_circ_141279,RMVar_hsa_circ_141281,RMVar_hsa_circ_271554,RMVar_hsa_circ_272738,RMVar_hsa_circ_327831,RMVar_hsa_circ_99497,RMVar_hsa_circ_141280,RMVar_hsa_circ_141278 39439 RMVar_ID_39439 Human_SNP_ID_56747785 A-to-I Human chr1 + 245063645 245063645 245063645 AGATTTAAGAGGTGCATTTCATTGGGAGGCTGAGGTGAGAGGATTGCTTGAGCTCAGGAATGAGG AGATTTAAGAGGTGCATTTCATTGGGAGGCTGCGGTGAGAGGATTGCTTGAGCTCAGGAATGAGG A C EFCAB2 Ensembl:ENSG00000203666 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs898927805 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_327831,RMVar_hsa_circ_270019,RMVar_hsa_circ_315676,RMVar_hsa_circ_141278,RMVar_hsa_circ_141284,RMVar_hsa_circ_141286,RMVar_hsa_circ_281721 39440 RMVar_ID_39440 Human_SNP_ID_56780147 A-to-I Human chr1 + 245191435 245191435 245191435 AGACAGAGGGTGCAGTGAGCCGAGATCACACCACTACACACCCACCTGGGCAATAAGAGTGAAAC AGACAGAGGGTGCAGTGAGCCGAGATCACACCGCTACACACCCACCTGGGCAATAAGAGTGAAAC A G KIF26B Ensembl:ENSG00000162849 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1438732254 Functional Loss SNV dbSNP153 33..33 33 - - - 39441 RMVar_ID_39441 Human_SNP_ID_56787800 A-to-I Human chr1 + 245222281 245222281 245222281 CAACATGGTAAAACCCCGTCTCTACTAAAAATACAAAAATTAGCCAGGTGTGGTGGTGGGTGTCT CAACATGGTAAAACCCCGTCTCTACTAAAAATTCAAAAATTAGCCAGGTGTGGTGGTGGGTGTCT A T KIF26B Ensembl:ENSG00000162849 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs551939357 Functional Loss SNV dbSNP153 33..33 33 - - - 39442 RMVar_ID_39442 Human_SNP_ID_56950251 A-to-I Human chr1 - 245849934 245849934 245849934 CAAGACAGTGAATAGGCCGGACACAGTGGCTCACGCTTGCAATCCCAGCACTTTGGGAGGCCAAG CAAGACAGTGAATAGGCCGGACACAGTGGCTCGCGCTTGCAATCCCAGCACTTTGGGAGGCCAAG T C SMYD3 Ensembl:ENSG00000185420 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1187164974 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21755,RMVar_hsa_circ_82632,RMVar_hsa_circ_121187,RMVar_hsa_circ_141299,RMVar_hsa_circ_141300,RMVar_hsa_circ_312973,RMVar_hsa_circ_364457,RMVar_hsa_circ_116043,RMVar_hsa_circ_141301,RMVar_hsa_circ_141302,RMVar_hsa_circ_141303,RMVar_hsa_circ_64099,RMVar_hsa_circ_307570 39443 RMVar_ID_39443 Human_SNP_ID_57026302 A-to-I Human chr1 - 246154902 246154902 246154902 TGGTAGGCGCCTGTAGTCCCAGCTTCTTATGAAGCTGAGGCAGGAGAATCACATGAACCCGGGAG TGGTAGGCGCCTGTAGTCCCAGCTTCTTATGAGGCTGAGGCAGGAGAATCACATGAACCCGGGAG T C SMYD3 Ensembl:ENSG00000185420 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1448617379 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 39444 RMVar_ID_39444 Human_SNP_ID_57030435 A-to-I Human chr1 - 246171806 246171806 246171806 AGGTCTTGCTATGTTGCCCAGTCTGGTCTCAAACTCCCGGCCTCAAGCAATTCCCCCACCTTGGC AGGTCTTGCTATGTTGCCCAGTCTGGTCTCAATCTCCCGGCCTCAAGCAATTCCCCCACCTTGGC T A SMYD3 Ensembl:ENSG00000185420 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1367604451 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557468 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 39445 RMVar_ID_39445 Human_SNP_ID_57033717 A-to-I Human chr1 - 246185361 246185361 246185361 GTGTTGGCGGGCACCTGCAGTCCCAGCTACTCAGGAGAATGAGGCAGGAGAATCGCTTGAACCCG GTGTTGGCGGGCACCTGCAGTCCCAGCTACTCGGGAGAATGAGGCAGGAGAATCGCTTGAACCCG T C SMYD3 Ensembl:ENSG00000185420 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1460888792 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 39446 RMVar_ID_39446 Human_SNP_ID_57050626 A-to-I Human chr1 - 246249232 246249220 246249232 AGGTGTGGTGGCAGGCGCCTGTACTCCCAGCTACTTGGAAGGCTGAGGCGGGAGAATCACTTAAA AGGTGTGGTGGCAGGCGCCTGTACTCCCAGCT____________GAGGCGGGAGAATCACTTAAA CAGCCTTCCAAGT C SMYD3 Ensembl:ENSG00000185420 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1430323884 Functional Loss DEL dbSNP153 33..44 33 - - - Human_RBP_ID_24674244 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_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 39447 RMVar_ID_39447 Human_SNP_ID_57054552 A-to-I Human chr1 - 246264404 246264404 246264404 CTGAAGCCATCCTCCTACCTTGGCTTCCCAAAATGCTGGGATTATAGGTATGAGCCATTGCACCC CTGAAGCCATCCTCCTACCTTGGCTTCCCAAAGTGCTGGGATTATAGGTATGAGCCATTGCACCC T C SMYD3 Ensembl:ENSG00000185420 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1051103835 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_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 39448 RMVar_ID_39448 Human_SNP_ID_57054776 A-to-I Human chr1 - 246265414 246265414 246265414 CGAAGCAGAACTGGATATAGTGGCTCATGCCTATAATCCTAGCACTTTGAGAGGCCAAGGAGGGA CGAAGCAGAACTGGATATAGTGGCTCATGCCTGTAATCCTAGCACTTTGAGAGGCCAAGGAGGGA T C SMYD3 Ensembl:ENSG00000185420 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,frontal_cortex - 29129909,30559470 RNA-Seq:(High) rs1440177092 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_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 39449 RMVar_ID_39449 Human_SNP_ID_57055113 A-to-I Human chr1 - 246266750 246266750 246266750 TGTCTTTCTTTCGGCTGGAGTGCACTGGTGCAATCTCGGCTCACTGCAACCTCCACCTCCCGGGT TGTCTTTCTTTCGGCTGGAGTGCACTGGTGCAGTCTCGGCTCACTGCAACCTCCACCTCCCGGGT T C SMYD3 Ensembl:ENSG00000185420 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1033628912 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19439723 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_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 39450 RMVar_ID_39450 Human_SNP_ID_57055599 A-to-I Human chr1 - 246268617 246268617 246268617 TGACTGCAACCTCCGCCTCCCAGGTTCAAGCTATTCCCCTGCCTCAGCCTCCCGGGTAGCTGGGA TGACTGCAACCTCCGCCTCCCAGGTTCAAGCTGTTCCCCTGCCTCAGCCTCCCGGGTAGCTGGGA T C SMYD3 Ensembl:ENSG00000185420 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1043309317 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_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 39451 RMVar_ID_39451 Human_SNP_ID_57064845 A-to-I Human chr1 - 246306235 246306235 246306235 TCGAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTATGGGACTACAGGCAGGCGCCAC TCGAGTGATTCTCCTGCCTCAGCCTCCCAAGTGGCTGGGACTATGGGACTACAGGCAGGCGCCAC T C SMYD3 Ensembl:ENSG00000185420 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1347976308 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10888337 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_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 39452 RMVar_ID_39452 Human_SNP_ID_57065904 A-to-I Human chr1 - 246310465 246310465 246310465 GGGAAAGCAGAAGTGTAAAATATAAGTGGGTAAGAGAAAGGGCAGCAACTTCCATTATTTTGCTC GGGAAAGCAGAAGTGTAAAATATAAGTGGGTATGAGAAAGGGCAGCAACTTCCATTATTTTGCTC T A SMYD3 Ensembl:ENSG00000185420 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1036513768 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_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 39453 RMVar_ID_39453 Human_SNP_ID_57067426 A-to-I Human chr1 - 246316873 246316873 246316873 CTCCTGCCTCAGCCTCCCGAGTATCTGGGACTACAGGCCGCACACCACCACGCCCAGCTAATTTT CTCCTGCCTCAGCCTCCCGAGTATCTGGGACTCCAGGCCGCACACCACCACGCCCAGCTAATTTT T G SMYD3 Ensembl:ENSG00000185420 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs902011753 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_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 39454 RMVar_ID_39454 Human_SNP_ID_57068496 A-to-I Human chr1 - 246321806 246321806 246321806 AAGTCGAGGCTGCAGTGAGCTGTGATCTCACCACTGCACTCCAGCCTGGACTACAAAGTGAGACC AAGTCGAGGCTGCAGTGAGCTGTGATCTCACCGCTGCACTCCAGCCTGGACTACAAAGTGAGACC T C SMYD3,SMYD3-IT1 Ensembl:ENSG00000185420,Ensembl:ENSG00000230184 Protein coding,lincRNA intron,exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1351751634 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_208036 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_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 39455 RMVar_ID_39455 Human_SNP_ID_57068497 A-to-I Human chr1 - 246321809 246321809 246321809 AGGAAGTCGAGGCTGCAGTGAGCTGTGATCTCACCACTGCACTCCAGCCTGGACTACAAAGTGAG AGGAAGTCGAGGCTGCAGTGAGCTGTGATCTCGCCACTGCACTCCAGCCTGGACTACAAAGTGAG T C SMYD3,SMYD3-IT1 Ensembl:ENSG00000185420,Ensembl:ENSG00000230184 Protein coding,lincRNA intron,exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs938006881 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24674407 Human_Splice_Rec_208036 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_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 39456 RMVar_ID_39456 Human_SNP_ID_57068594 A-to-I Human chr1 - 246322200 246322200 246322200 CACCACACCGGGCTAATTTTTGTATTTTTAGTAGAGATGGGCTTTTGTCATGTTGGCCAGGCTGG CACCACACCGGGCTAATTTTTGTATTTTTAGTGGAGATGGGCTTTTGTCATGTTGGCCAGGCTGG T C SMYD3,SMYD3-IT1 Ensembl:ENSG00000185420,Ensembl:ENSG00000230184 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893570083 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_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 39457 RMVar_ID_39457 Human_SNP_ID_57068620 A-to-I Human chr1 - 246322310 246322310 246322310 CAGGCTGGAGTGCAGTAGCGTGATCTCGGCTCACTGCACCTCTGCCTCCTGGCTTTCAAGTTGAG CAGGCTGGAGTGCAGTAGCGTGATCTCGGCTCGCTGCACCTCTGCCTCCTGGCTTTCAAGTTGAG T C SMYD3,SMYD3-IT1 Ensembl:ENSG00000185420,Ensembl:ENSG00000230184 Protein coding,lincRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1021232185 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_208035 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_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 39458 RMVar_ID_39458 Human_SNP_ID_57069252 A-to-I Human chr1 - 246324731 246324731 246324731 AGAAGAAACGGGCACCATAAAAAAATAACATAAAACAGGATTTTGTTTATTGAGGCCAGGTAAAG AGAAGAAACGGGCACCATAAAAAAATAACATATAACAGGATTTTGTTTATTGAGGCCAGGTAAAG T A SMYD3 Ensembl:ENSG00000185420 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs969099239 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_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 39459 RMVar_ID_39459 Human_SNP_ID_57069253 A-to-I Human chr1 - 246324731 246324731 246324731 AGAAGAAACGGGCACCATAAAAAAATAACATAAAACAGGATTTTGTTTATTGAGGCCAGGTAAAG AGAAGAAACGGGCACCATAAAAAAATAACATAGAACAGGATTTTGTTTATTGAGGCCAGGTAAAG T C SMYD3 Ensembl:ENSG00000185420 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs969099239 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_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 39460 RMVar_ID_39460 Human_SNP_ID_57069847 A-to-I Human chr1 + 246326684 246326684 246326684 TACTCAGAATGCTGAGGCATGAGACTCGCTTGATTCTGGGAGGCGGAGATTGCAGTGAGCCGAGA TACTCAGAATGCTGAGGCATGAGACTCGCTTGGTTCTGGGAGGCGGAGATTGCAGTGAGCCGAGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs367787876 Functional Loss SNV dbSNP153 33..33 33 - - - 39461 RMVar_ID_39461 Human_SNP_ID_57104184 A-to-I Human chr1 - 246464361 246464361 246464361 AGGCACATGCCACCACTCCTGGCTAAGTTTTTAAATTTTTAGTAGAGATGGGGTTTTGCCATGGT AGGCACATGCCACCACTCCTGGCTAAGTTTTTTAATTTTTAGTAGAGATGGGGTTTTGCCATGGT T A SMYD3 Ensembl:ENSG00000185420 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs948502482 Functional Loss SNV dbSNP153 33..33 33 - - - 39462 RMVar_ID_39462 Human_SNP_ID_57108543 A-to-I Human chr1 - 246481897 246481897 246481897 CTGCTTTGGCCTCCCAAAGTGCTGGGATTGCAAGTGTGAGCCATTACACCCAGCCAGAAGTTATG CTGCTTTGGCCTCCCAAAGTGCTGGGATTGCAGGTGTGAGCCATTACACCCAGCCAGAAGTTATG T C SMYD3 Ensembl:ENSG00000185420 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs916239515 Functional Loss SNV dbSNP153 33..33 33 - - - 39463 RMVar_ID_39463 Human_SNP_ID_57113031 A-to-I Human chr1 - 246499593 246499593 246499593 AAATTAGCCAGATGTGGTGGTGCATGCCTGTAATCAAGCTACTTTGGAGGCTGAGGCAGGAGAAT AAATTAGCCAGATGTGGTGGTGCATGCCTGTAGTCAAGCTACTTTGGAGGCTGAGGCAGGAGAAT T C SMYD3 Ensembl:ENSG00000185420 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1193341729 Functional Loss SNV dbSNP153 33..33 33 - - - 39464 RMVar_ID_39464 Human_SNP_ID_57113032 A-to-I Human chr1 - 246499593 246499593 246499593 AAATTAGCCAGATGTGGTGGTGCATGCCTGTAATCAAGCTACTTTGGAGGCTGAGGCAGGAGAAT AAATTAGCCAGATGTGGTGGTGCATGCCTGTACTCAAGCTACTTTGGAGGCTGAGGCAGGAGAAT T G SMYD3 Ensembl:ENSG00000185420 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1193341729 Functional Loss SNV dbSNP153 33..33 33 - - - 39465 RMVar_ID_39465 Human_SNP_ID_57128383 A-to-I Human chr1 - 246553023 246553023 246553023 TACAGATGGGGTTTCACCATGTTGGTCAGGCTAGTCTCAAACTGGTGACCTCATGATCCGCCTGC TACAGATGGGGTTTCACCATGTTGGTCAGGCTGGTCTCAAACTGGTGACCTCATGATCCGCCTGC T C TFB2M Ensembl:ENSG00000162851 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1245905744 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10890192 RMVar_hsa_circ_141336,RMVar_hsa_circ_141337,RMVar_hsa_circ_141340,RMVar_hsa_circ_296948,RMVar_hsa_circ_284622,RMVar_hsa_circ_141342,RMVar_hsa_circ_141343,RMVar_hsa_circ_141345,RMVar_hsa_circ_19800,RMVar_hsa_circ_296411,RMVar_hsa_circ_270316,RMVar_hsa_circ_357315,RMVar_hsa_circ_141344 39466 RMVar_ID_39466 Human_SNP_ID_57129800 A-to-I Human chr1 - 246558239 246558239 246558239 GTGGGACTGAGGTGGAAGGATCACTTAAGCCCAGGAGGTCAAGGCTGCAGTCAGCTGGGATTGCG GTGGGACTGAGGTGGAAGGATCACTTAAGCCCGGGAGGTCAAGGCTGCAGTCAGCTGGGATTGCG T C TFB2M Ensembl:ENSG00000162851 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs376055394 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13690,RMVar_hsa_circ_19800 39467 RMVar_ID_39467 Human_SNP_ID_57130012 A-to-I Human chr1 - 246559235 246559235 246559235 CAAAATTTACTACATTTTGAGCTGGACACGGTATCACACACCTGTAATCCCAGACACTTAGGAGG CAAAATTTACTACATTTTGAGCTGGACACGGTTTCACACACCTGTAATCCCAGACACTTAGGAGG T A TFB2M Ensembl:ENSG00000162851 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs777312247 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13690,RMVar_hsa_circ_19800 39468 RMVar_ID_39468 Human_SNP_ID_57130013 A-to-I Human chr1 - 246559235 246559235 246559235 CAAAATTTACTACATTTTGAGCTGGACACGGTATCACACACCTGTAATCCCAGACACTTAGGAGG CAAAATTTACTACATTTTGAGCTGGACACGGTGTCACACACCTGTAATCCCAGACACTTAGGAGG T C TFB2M Ensembl:ENSG00000162851 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs777312247 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13690,RMVar_hsa_circ_19800 39469 RMVar_ID_39469 Human_SNP_ID_57130919 A-to-I Human chr1 - 246562839 246562839 246562839 CCTGACCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAACTTAGCTGGGCGTGGTGGCGC CCTGACCAACATGGTGAAACCCCGTCTCTACTCAAAATACAAAACTTAGCTGGGCGTGGTGGCGC T G TFB2M Ensembl:ENSG00000162851 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1266927311 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_102307 RMVar_hsa_circ_13690,RMVar_hsa_circ_19800 39470 RMVar_ID_39470 Human_SNP_ID_57139238 A-to-I Human chr1 + 246593862 246593862 246593862 ATGGCTCTCTGCAGCCTTGATCTCCCAGGCACAAGCGATTCTCCCACCTCAGCCTCTGGAGTAGC ATGGCTCTCTGCAGCCTTGATCTCCCAGGCACTAGCGATTCTCCCACCTCAGCCTCTGGAGTAGC A T CNST Ensembl:ENSG00000162852 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1279583228 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15200,RMVar_hsa_circ_365412,RMVar_hsa_circ_119269,RMVar_hsa_circ_141348,RMVar_hsa_circ_368979,RMVar_hsa_circ_350620,RMVar_hsa_circ_61240 39471 RMVar_ID_39471 Human_SNP_ID_57157294 A-to-I Human chr1 + 246660990 246660990 246660990 TTTGTCTTTTGTTGTTTTTTTGTTTTTTTTTTAAGACGGTCTTGCTCTGTCACCCAGGCTGGATT TTTGTCTTTTGTTGTTTTTTTGTTTTTTTTTTGAGACGGTCTTGCTCTGTCACCCAGGCTGGATT A G CNST Ensembl:ENSG00000162852 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1323215561 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10890798 39472 RMVar_ID_39472 Human_SNP_ID_57157318 A-to-I Human chr1 + 246661063 246661063 246661063 GCAAATCACTGCAACCTCAACCTCCACCTCCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTG GCAAATCACTGCAACCTCAACCTCCACCTCCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTG A G CNST Ensembl:ENSG00000162852 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1455343552 Functional Loss SNV dbSNP153 33..33 33 - - - 39473 RMVar_ID_39473 Human_SNP_ID_57157364 A-to-I Human chr1 + 246661236 246661236 246661236 ATGAGGTTAGGATCTGCCTGCCTTGGCCTCCCAAAGTGCTAGGATTACAGGTGTGAGCCACCGCA ATGAGGTTAGGATCTGCCTGCCTTGGCCTCCCGAAGTGCTAGGATTACAGGTGTGAGCCACCGCA A G CNST Ensembl:ENSG00000162852 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1331395623 Functional Loss SNV dbSNP153 33..33 33 - - - 39474 RMVar_ID_39474 Human_SNP_ID_57157386 A-to-I Human chr1 + 246661332 246661332 246661332 TAGAGATGAGGTTTTGCCATGTTGGCCAGGCTAGTCTCGAACTCCTGGCTTCAAGTGATCCACCC TAGAGATGAGGTTTTGCCATGTTGGCCAGGCTGGTCTCGAACTCCTGGCTTCAAGTGATCCACCC A G CNST Ensembl:ENSG00000162852 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1166449473 Functional Loss SNV dbSNP153 33..33 33 - - - 39475 RMVar_ID_39475 Human_SNP_ID_57157397 A-to-I Human chr1 + 246661392 246661392 246661392 CACCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCATGCCCGGCTTGTCTTC CACCCACCTCGGCCTCCCAAAGTGCTGGGATTCCAGGCATGAGCCACCATGCCCGGCTTGTCTTC A C CNST Ensembl:ENSG00000162852 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1035429929 Functional Loss SNV dbSNP153 33..33 33 - - - 39476 RMVar_ID_39476 Human_SNP_ID_57178594 A-to-I Human chr1 + 246737934 246737934 246737934 AACCTAATAAGGAGTTGGGCACGTTGGCTCATACCTGTAATCTCAGCACTCTGGGAAGCCAAAGT AACCTAATAAGGAGTTGGGCACGTTGGCTCATGCCTGTAATCTCAGCACTCTGGGAAGCCAAAGT A G SCCPDH Ensembl:ENSG00000143653 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1412288294 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73411,RMVar_hsa_circ_304985,RMVar_hsa_circ_109819,RMVar_hsa_circ_363310,RMVar_hsa_circ_141357,RMVar_hsa_circ_358219,RMVar_hsa_circ_287905,RMVar_hsa_circ_297657,RMVar_hsa_circ_141358,RMVar_hsa_circ_141360,RMVar_hsa_circ_54513,RMVar_hsa_circ_141359,RMVar_hsa_circ_141365,RMVar_hsa_circ_281703,RMVar_hsa_circ_366024,RMVar_hsa_circ_141362,RMVar_hsa_circ_330503,RMVar_hsa_circ_277565,RMVar_hsa_circ_141363,RMVar_hsa_circ_141364 39477 RMVar_ID_39477 Human_SNP_ID_57189812 A-to-I Human chr1 + 246783913 246783913 246783913 CGGGGTTTCACCATGTTGCCCAAGCTGGTCTCAAACTCCTGAGCTCAAGCCATCCACCCACCTCG CGGGGTTTCACCATGTTGCCCAAGCTGGTCTCCAACTCCTGAGCTCAAGCCATCCACCCACCTCG A C LINC01341 Ensembl:ENSG00000227953 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1291814311 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5092318 Human_Splice_Rec_208260 39478 RMVar_ID_39478 Human_SNP_ID_57191027 A-to-I Human chr1 + 246787576 246787576 246787576 CACCTCCCAGACTCAAGCAATCCTCCCATCTCAGCCTGCTGAGTACCTGGGACTACGGGTGCAAG CACCTCCCAGACTCAAGCAATCCTCCCATCTCGGCCTGCTGAGTACCTGGGACTACGGGTGCAAG A G LINC01341 Ensembl:ENSG00000227953 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs557093572 Functional Loss SNV dbSNP153 33..33 33 - - - 39479 RMVar_ID_39479 Human_SNP_ID_57191054 A-to-I Human chr1 + 246787688 246787688 246787688 CACTTTGTTTCCCAGGCTGGTCTTGAACTCCCAGGTTCAAGCGATCCTCCTGCCTTGGCCTCTCA CACTTTGTTTCCCAGGCTGGTCTTGAACTCCCTGGTTCAAGCGATCCTCCTGCCTTGGCCTCTCA A T LINC01341 Ensembl:ENSG00000227953 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1023150666 Functional Loss SNV dbSNP153 33..33 33 - - - 39480 RMVar_ID_39480 Human_SNP_ID_57206385 A-to-I Human chr1 - 246842337 246842337 246842337 TCTCAAGTGATCCGCCTGCCTTGGCCTCCCATAGTGCTTGGATGACAGGTGTGAGCCACTGCACC TCTCAAGTGATCCGCCTGCCTTGGCCTCCCATGGTGCTTGGATGACAGGTGTGAGCCACTGCACC T C AHCTF1 Ensembl:ENSG00000153207 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1011369272 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265981 39481 RMVar_ID_39481 Human_SNP_ID_57206437 A-to-I Human chr1 - 246842525 246842525 246842525 AAGGCTGGAGTGCAGTGGTGTGATTTCGGCTCACTGCAACCTCTGCCTCCCAGGTTCAGGTGATT AAGGCTGGAGTGCAGTGGTGTGATTTCGGCTCTCTGCAACCTCTGCCTCCCAGGTTCAGGTGATT T A AHCTF1 Ensembl:ENSG00000153207 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1287423278 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265981 39482 RMVar_ID_39482 Human_SNP_ID_57229379 A-to-I Human chr1 - 246922194 246922194 246922194 TGCCATGCCCGACTGATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATACTGGTTGGGCTGA TGCCATGCCCGACTGATTTTTGTATTTTTAGTGGAGATGGGGTTTCACCATACTGGTTGGGCTGA T C AHCTF1 Ensembl:ENSG00000153207 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1176111526 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10893255 39483 RMVar_ID_39483 Human_SNP_ID_57229488 A-to-I Human chr1 - 246922572 246922572 246922572 ATGGGCAACATAGTGAGACCTTATTTCTACTAAAAAAAAAAAATTAGCCAGGCATGGTGGCACGA ATGGGCAACATAGTGAGACCTTATTTCTACTACAAAAAAAAAATTAGCCAGGCATGGTGGCACGA T G AHCTF1 Ensembl:ENSG00000153207 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1047187274 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10893268 39484 RMVar_ID_39484 Human_SNP_ID_57235566 A-to-I Human chr1 - 246943107 246943107 246943107 CTGCGGCACTGCACTCTAGCCTGGGCAACAGAATGAGACTCCATCTCAAAATAAATTTTAAAAAT CTGCGGCACTGCACTCTAGCCTGGGCAACAGAGTGAGACTCCATCTCAAAATAAATTTTAAAAAT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1489177854 Functional Loss SNV dbSNP153 33..33 33 - - - 39485 RMVar_ID_39485 Human_SNP_ID_57276333 A-to-I Human chr1 - 247098385 247098385 247098385 ACTATGTCCAGCTAATTTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCTAGGCTGG ACTATGTCCAGCTAATTTTTTGTATTTTTAGTGGAGACAGGGTTTCACCATGTTGGCTAGGCTGG T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs545667714 Functional Loss SNV dbSNP153 33..33 33 - - - 39486 RMVar_ID_39486 Human_SNP_ID_57276334 A-to-I Human chr1 - 247098394 247098387 247098394 GCGCCCACCACTATGTCCAGCTAATTTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGG GCGCCCACCACTATGTCCAGCTAATTTTTTGT_______GTAGAGACAGGGTTTCACCATGTTGG CTAAAAAT C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1211755612 Functional Loss DEL dbSNP153 33..39 33 - - - 39487 RMVar_ID_39487 Human_SNP_ID_57276337 A-to-I Human chr1 - 247098394 247098394 247098394 GCGCCCACCACTATGTCCAGCTAATTTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGG GCGCCCACCACTATGTCCAGCTAATTTTTTGTGTTTTTAGTAGAGACAGGGTTTCACCATGTTGG T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1283833121 Functional Loss SNV dbSNP153 33..33 33 - - - 39488 RMVar_ID_39488 Human_SNP_ID_57276973 A-to-I Human chr1 - 247100415 247100415 247100415 ATATAGAGGCTGGGTGTAGTGACTCAGCCTATAATCCCAGCACTTTGGGAGGCCAAGGCGTGTGG ATATAGAGGCTGGGTGTAGTGACTCAGCCTATTATCCCAGCACTTTGGGAGGCCAAGGCGTGTGG T A ZNF669 Ensembl:ENSG00000188295 Protein coding CDS GSE56152 embryonic stem cells,wild type - 25708366 RNA-Seq:(High) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_17746608 39489 RMVar_ID_39489 Human_SNP_ID_57276974 A-to-I Human chr1 - 247100417 247100417 247100417 TGATATAGAGGCTGGGTGTAGTGACTCAGCCTATAATCCCAGCACTTTGGGAGGCCAAGGCGTGT TGATATAGAGGCTGGGTGTAGTGACTCAGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGTGT T C ZNF669 Ensembl:ENSG00000188295 Protein coding CDS GSE56152 embryonic stem cells,wild type - 25708366 RNA-Seq:(High) rs17856483 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17746608 39490 RMVar_ID_39490 Human_SNP_ID_57288856 A-to-I Human chr1 - 247146444 247146444 247146444 ACAGAACTCCAGTCAAACTGAATCCAAACTCAAGGAGGGCTGGGGGCTGCCTAGCTTTGTATTCC ACAGAACTCCAGTCAAACTGAATCCAAACTCAGGGAGGGCTGGGGGCTGCCTAGCTTTGTATTCC T C ZNF124 Ensembl:ENSG00000196418 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1461057874 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112889,RMVar_hsa_circ_98886,RMVar_hsa_circ_141412,RMVar_hsa_circ_141413 39491 RMVar_ID_39491 Human_SNP_ID_57292030 A-to-I Human chr1 - 247158106 247158106 247158106 AGCTGGGATTACAGGAACATGCCACCACACCCAGCTAATTTTTGTATTTTTAGTAGAGACAGCAT AGCTGGGATTACAGGAACATGCCACCACACCCGGCTAATTTTTGTATTTTTAGTAGAGACAGCAT T C ZNF124 Ensembl:ENSG00000196418 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1230972279 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124344,RMVar_hsa_circ_112889,RMVar_hsa_circ_98886,RMVar_hsa_circ_141412,RMVar_hsa_circ_141413,RMVar_hsa_circ_141416,RMVar_hsa_circ_141414,RMVar_hsa_circ_141415,RMVar_hsa_circ_141417,RMVar_hsa_circ_141421,RMVar_hsa_circ_376867 39492 RMVar_ID_39492 Human_SNP_ID_57292180 A-to-I Human chr1 - 247158705 247158705 247158705 GAATTGCTTGAACCTGGGAGGCGGAGGTTGCAATGAGCTGAGGTTGTGCCATTGCACTCCAGCCA GAATTGCTTGAACCTGGGAGGCGGAGGTTGCAGTGAGCTGAGGTTGTGCCATTGCACTCCAGCCA T C ZNF124 Ensembl:ENSG00000196418 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1156700963 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124344,RMVar_hsa_circ_112889,RMVar_hsa_circ_98886,RMVar_hsa_circ_141412,RMVar_hsa_circ_141413,RMVar_hsa_circ_141416,RMVar_hsa_circ_141414,RMVar_hsa_circ_141415,RMVar_hsa_circ_141417,RMVar_hsa_circ_141421,RMVar_hsa_circ_376867 39493 RMVar_ID_39493 Human_SNP_ID_57298769 A-to-I Human chr1 - 247184353 247184353 247184353 GGCTGGCGGGGCAGGACTGGGCGCCAGCAAGCATATCTTGGGATCTCTGTTGTCTGACTCCCTGT GGCTGGCGGGGCAGGACTGGGCGCCAGCAAGCGTATCTTGGGATCTCTGTTGTCTGACTCCCTGT T C AL390728.2 Ensembl:ENSG00000215795 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1297905742 Functional Loss SNV dbSNP153 33..33 33 - - - 39494 RMVar_ID_39494 Human_SNP_ID_57303105 A-to-I Human chr1 - 247201204 247201204 247201204 CCAGCTATTTGGGAGGCTGAGGTGGGAGAATCACTGGAACCTGGGAAGCAGAGGCTGCAGTGAGC CCAGCTATTTGGGAGGCTGAGGTGGGAGAATCGCTGGAACCTGGGAAGCAGAGGCTGCAGTGAGC T C AL390728.4 Ensembl:ENSG00000227671 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1333214420 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24674996 39495 RMVar_ID_39495 Human_SNP_ID_57304257 A-to-I Human chr1 - 247205820 247205818 247205820 TTTTTATTTTGTGTAGGGGTGAGATCTCACTTATGTTGCCCTGGATGGTCTCGAACTCCTGGCTT TTTTTATTTTGTGTAGGGGTGAGATCTCACTT__GTTGCCCTGGATGGTCTCGAACTCCTGGCTT CAT C AL390728.4 Ensembl:ENSG00000227671 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1020069700 Functional Loss DEL dbSNP153 33..34 33 - - - 39496 RMVar_ID_39496 Human_SNP_ID_57328130 A-to-I Human chr1 - 247305212 247305212 247305212 AGAGAACAGTGGCGCGATCTTGGCTTACTGCAACCTCTGCCTCCCGTGTTCCAGCAATTTTCCTG AGAGAACAGTGGCGCGATCTTGGCTTACTGCAGCCTCTGCCTCCCGTGTTCCAGCAATTTTCCTG T C ZNF496 Ensembl:ENSG00000162714 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs781414817 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96820,RMVar_hsa_circ_141426,RMVar_hsa_circ_141424,RMVar_hsa_circ_127213 39497 RMVar_ID_39497 Human_SNP_ID_57332176 A-to-I Human chr1 - 247321013 247321013 247321013 CGCAACCACGCTTGGCTAATTTTTGTATTCTTAGTAGAGACGGGGTTTCACCATGTTAGTCAGGC CGCAACCACGCTTGGCTAATTTTTGTATTCTTGGTAGAGACGGGGTTTCACCATGTTAGTCAGGC T C ZNF496 Ensembl:ENSG00000162714 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1441732514 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73657 39498 RMVar_ID_39498 Human_SNP_ID_57337622 A-to-I Human chr1 + 247341267 247341267 247341267 ACCGCTCATTGTAGCCTCTACATCCTGGACTCAAGCAATCCTCCCACCTCAGCCTCTCAAGTAGC ACCGCTCATTGTAGCCTCTACATCCTGGACTCCAGCAATCCTCCCACCTCAGCCTCTCAAGTAGC A C lnc-NLRP3-1,lnc-NLRP3-1:2,lnc-NLRP3-1:3 RNACentral:URS00008B71DA,RNACentral:URS00008BDC22,RNACentral:URS00009C11AD lincRNA,lincRNA,lincRNA intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs760791498 Functional Loss SNV dbSNP153 33..33 33 - - - 39499 RMVar_ID_39499 Human_SNP_ID_57337623 A-to-I Human chr1 + 247341267 247341267 247341267 ACCGCTCATTGTAGCCTCTACATCCTGGACTCAAGCAATCCTCCCACCTCAGCCTCTCAAGTAGC ACCGCTCATTGTAGCCTCTACATCCTGGACTCGAGCAATCCTCCCACCTCAGCCTCTCAAGTAGC A G lnc-NLRP3-1,lnc-NLRP3-1:2,lnc-NLRP3-1:3 RNACentral:URS00008B71DA,RNACentral:URS00008BDC22,RNACentral:URS00009C11AD lincRNA,lincRNA,lincRNA intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs760791498 Functional Loss SNV dbSNP153 33..33 33 - - - 39500 RMVar_ID_39500 Human_SNP_ID_57337652 A-to-I Human chr1 + 247341403 247341403 247341403 GTTGCTCAGGTTGGTCTCGAACTCTTGGGCTCAAGGCATCCTCTCACCTCGGCCTCTCAAAGTCT GTTGCTCAGGTTGGTCTCGAACTCTTGGGCTCGAGGCATCCTCTCACCTCGGCCTCTCAAAGTCT A G lnc-NLRP3-1,lnc-NLRP3-1:2,lnc-NLRP3-1:3 RNACentral:URS00008B71DA,RNACentral:URS00008BDC22,RNACentral:URS00009C11AD lincRNA,lincRNA,lincRNA intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs912219992 Functional Loss SNV dbSNP153 33..33 33 - - - 39501 RMVar_ID_39501 Human_SNP_ID_57338562 A-to-I Human chr1 + 247344715 247344715 247344715 TGTTAGAAGAAGGCAGGACTAGGCCGGGTGTCATGGCTCCCACCTGTAATCCCAGCACTTTGGGA TGTTAGAAGAAGGCAGGACTAGGCCGGGTGTCTTGGCTCCCACCTGTAATCCCAGCACTTTGGGA A T lnc-NLRP3-1,lnc-NLRP3-1:2,lnc-NLRP3-1:3 RNACentral:URS00008B71DA,RNACentral:URS00008BDC22,RNACentral:URS00009C11AD lincRNA,lincRNA,lincRNA intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1439446385 Functional Loss SNV dbSNP153 33..33 33 - - - 39502 RMVar_ID_39502 Human_SNP_ID_57339269 A-to-I Human chr1 + 247347397 247347397 247347397 GGGAGGCAGAGGTTGCAGTGAGCTGAGACCGCACCACTCTATTCCAGCCTGGACAATAGAGCGAG GGGAGGCAGAGGTTGCAGTGAGCTGAGACCGCCCCACTCTATTCCAGCCTGGACAATAGAGCGAG A C lnc-NLRP3-1,lnc-NLRP3-1:2,lnc-NLRP3-1:3 RNACentral:URS00008B71DA,RNACentral:URS00008BDC22,RNACentral:URS00009C11AD lincRNA,lincRNA,lincRNA intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1288355796 Functional Loss SNV dbSNP153 33..33 33 - - - 39503 RMVar_ID_39503 Human_SNP_ID_57340908 A-to-I Human chr1 + 247353763 247353763 247353763 CCTGTAATCCCAGCATCTCGGAAGGCTGAGGCAGGTGGATCACCTGAGGTCAGGAGTTCGAGACT CCTGTAATCCCAGCATCTCGGAAGGCTGAGGCGGGTGGATCACCTGAGGTCAGGAGTTCGAGACT A G lnc-NLRP3-1,lnc-NLRP3-1:2,lnc-NLRP3-1:3 RNACentral:URS00008B71DA,RNACentral:URS00008BDC22,RNACentral:URS00009C11AD lincRNA,lincRNA,lincRNA intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1303058876 Functional Loss SNV dbSNP153 33..33 33 - - - 39504 RMVar_ID_39504 Human_SNP_ID_57503051 A-to-I Human chr1 + 247994276 247994276 247994276 AAAATTAGCCGGGCGTGGTGGCGGGCGCCTGTAGTCCCGGCTGCTTGAGAGGCTGAGGCAGGAGA AAAATTAGCCGGGCGTGGTGGCGGGCGCCTGTGGTCCCGGCTGCTTGAGAGGCTGAGGCAGGAGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928590106 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_141431 39505 RMVar_ID_39505 Human_SNP_ID_57726432 A-to-I Human chr1 + 248842410 248842410 248842410 TGTGGAGAAGGTATGGATGTGAACAGGGAGAGAACATACATAGTGGGAGTTTATCCTGTCCCTTT TGTGGAGAAGGTATGGATGTGAACAGGGAGAGTACATACATAGTGGGAGTTTATCCTGTCCCTTT A T ZNF672 Ensembl:ENSG00000171161 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1366728833 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_141436,RMVar_hsa_circ_92551 39506 RMVar_ID_39506 Human_SNP_ID_625310487 A-to-I Human chr17 - 45025814 45025797 45025814 CTGGAGGATAGAGGTTGCAGTGAGCCAAGATCACGCCACTGCACTCCAGCCTGGGCGACAGAGTG CTGGAGGATAGAGGTTGCAGTGAGCCAAGATC_________________CCTGGGCGACAGAGTG GCTGGAGTGCAGTGGCGT G DCAKD Ensembl:ENSG00000172992 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs770613397 Functional Loss DEL dbSNP153 33..49 33 - - - Human_RBP_ID_25342760 RMVar_hsa_circ_79331,RMVar_hsa_circ_184783 39507 RMVar_ID_39507 Human_SNP_ID_625310573 A-to-I Human chr17 - 45026138 45026138 45026138 AAGGCGGGTGGATCACCTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAATCCCGT AAGGCGGGTGGATCACCTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAATCCCGT T C DCAKD Ensembl:ENSG00000172992 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1176715745 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79331,RMVar_hsa_circ_184783 39508 RMVar_ID_39508 Human_SNP_ID_625310577 A-to-I Human chr17 - 45026146 45026146 45026146 GGGAGGCCAAGGCGGGTGGATCACCTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGGTGA GGGAGGCCAAGGCGGGTGGATCACCTGAGGTCCGGAGTTCAAGACCAGCCTGGCCAACATGGTGA T G DCAKD Ensembl:ENSG00000172992 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1486140920 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79331,RMVar_hsa_circ_184783 39509 RMVar_ID_39509 Human_SNP_ID_625312137 A-to-I Human chr17 - 45032530 45032530 45032530 TATGCCTGCCTCGCCCTCCCAAAGTGCTGGGAATACAAGCGTGAGCCACTGTGCCTGGCTGGGGG TATGCCTGCCTCGCCCTCCCAAAGTGCTGGGATTACAAGCGTGAGCCACTGTGCCTGGCTGGGGG T A DCAKD Ensembl:ENSG00000172992 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1173774444 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27037,RMVar_hsa_circ_79331,RMVar_hsa_circ_184783,RMVar_hsa_circ_277271,RMVar_hsa_circ_334488,RMVar_hsa_circ_86883,RMVar_hsa_circ_184784,RMVar_hsa_circ_184785 39510 RMVar_ID_39510 Human_SNP_ID_625312359 A-to-I Human chr17 - 45033500 45033500 45033500 AGATTGCACCCTATACTCAGACTGTCTGGGCAACAGAGCAAGACTCCGTCTCAAAAAAAAGAAAA AGATTGCACCCTATACTCAGACTGTCTGGGCAGCAGAGCAAGACTCCGTCTCAAAAAAAAGAAAA T C DCAKD Ensembl:ENSG00000172992 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934099978 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27037,RMVar_hsa_circ_79331,RMVar_hsa_circ_184783,RMVar_hsa_circ_277271,RMVar_hsa_circ_334488,RMVar_hsa_circ_86883,RMVar_hsa_circ_184784,RMVar_hsa_circ_184785 39511 RMVar_ID_39511 Human_SNP_ID_625314589 A-to-I Human chr17 - 45041947 45041947 45041947 CATGCCCAGCTATTTTTTTTTTTTTAAGAGACAGGATCTCGCTTTGTTGCCCAGGCTGGCCTCTA CATGCCCAGCTATTTTTTTTTTTTTAAGAGACGGGATCTCGCTTTGTTGCCCAGGCTGGCCTCTA T C DCAKD Ensembl:ENSG00000172992 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1028919555 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13029959 RMVar_hsa_circ_79331,RMVar_hsa_circ_184783,RMVar_hsa_circ_86883,RMVar_hsa_circ_184785 39512 RMVar_ID_39512 Human_SNP_ID_625314633 A-to-I Human chr17 - 45042113 45042113 45042113 GACAATGATGTGCCTGTCACTCTTTTTTTTTTAAGTCAGGTCTTATTCTGCACCCAGGCTGGAGT GACAATGATGTGCCTGTCACTCTTTTTTTTTTGAGTCAGGTCTTATTCTGCACCCAGGCTGGAGT T C DCAKD Ensembl:ENSG00000172992 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs982080774 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13029961 RMVar_hsa_circ_79331,RMVar_hsa_circ_184783,RMVar_hsa_circ_86883,RMVar_hsa_circ_184785 39513 RMVar_ID_39513 Human_SNP_ID_625315200 A-to-I Human chr17 - 45044447 45044447 45044447 CCTCAGGTGACCCGCCTGCCTCAGCCTCCGAAAGTGTTGGGATTACAGGCGTCAGCCACCGCACC CCTCAGGTGACCCGCCTGCCTCAGCCTCCGAAGGTGTTGGGATTACAGGCGTCAGCCACCGCACC T C DCAKD Ensembl:ENSG00000172992 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1014114838 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22717440 RMVar_hsa_circ_79331,RMVar_hsa_circ_184783,RMVar_hsa_circ_86883,RMVar_hsa_circ_184785 39514 RMVar_ID_39514 Human_SNP_ID_625315637 A-to-I Human chr17 - 45045962 45045962 45045962 AAAATTAGCTGGGCGTGGTGGCAGTGGCTGTAATCCAGCTACTCGGGAGGCTGAGGCAGGAGAAT AAAATTAGCTGGGCGTGGTGGCAGTGGCTGTAGTCCAGCTACTCGGGAGGCTGAGGCAGGAGAAT T C DCAKD Ensembl:ENSG00000172992 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs190886676 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79331,RMVar_hsa_circ_184783,RMVar_hsa_circ_86883,RMVar_hsa_circ_184785 39515 RMVar_ID_39515 Human_SNP_ID_625316476 A-to-I Human chr17 - 45048982 45048982 45048982 GACCTCTTGGGCTCAAGCAATACTCCCACCTTAGCTTCCCCAGTAGCTGGGACTGCAGGCTTTCG GACCTCTTGGGCTCAAGCAATACTCCCACCTTGGCTTCCCCAGTAGCTGGGACTGCAGGCTTTCG T C DCAKD Ensembl:ENSG00000172992 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350857650 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13030121 RMVar_hsa_circ_79331,RMVar_hsa_circ_184783,RMVar_hsa_circ_86883,RMVar_hsa_circ_184785 39516 RMVar_ID_39516 Human_SNP_ID_625317768 A-to-I Human chr17 - 45052856 45052856 45052856 CCCGGCCTAGATGCTTTATTTTTTTTGAGGCAAGGTCTCGTTTTGTTGCCCAGGCTGGAGTGCAG CCCGGCCTAGATGCTTTATTTTTTTTGAGGCATGGTCTCGTTTTGTTGCCCAGGCTGGAGTGCAG T A DCAKD Ensembl:ENSG00000172992 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1242766207 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17566893,Human_RBP_ID_18699534 RMVar_hsa_circ_79331,RMVar_hsa_circ_184783,RMVar_hsa_circ_86883,RMVar_hsa_circ_184785 39517 RMVar_ID_39517 Human_SNP_ID_625318637 A-to-I Human chr17 - 45056109 45056109 45056109 CTCTTTTTGCCTAGGCTGGAGTGCAATGGTGCAATCTCTCCTCACTGCAACCTCTGCCTCCTGAG CTCTTTTTGCCTAGGCTGGAGTGCAATGGTGCCATCTCTCCTCACTGCAACCTCTGCCTCCTGAG T G DCAKD Ensembl:ENSG00000172992 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1209289216 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79331,RMVar_hsa_circ_184783,RMVar_hsa_circ_86883,RMVar_hsa_circ_184785 39518 RMVar_ID_39518 Human_SNP_ID_625318993 A-to-I Human chr17 - 45057242 45057242 45057242 GCCCAGGAGTGTGAGACCTGCCTGGGCAACATAGAGGACCCTGTCTCTAAAAAAAATACAAAAAT GCCCAGGAGTGTGAGACCTGCCTGGGCAACATGGAGGACCCTGTCTCTAAAAAAAATACAAAAAT T C DCAKD Ensembl:ENSG00000172992 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1240839752 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22475664 RMVar_hsa_circ_79331,RMVar_hsa_circ_184783,RMVar_hsa_circ_86883,RMVar_hsa_circ_184785 39519 RMVar_ID_39519 Human_SNP_ID_625319090 A-to-I Human chr17 - 45057617 45057617 45057617 CTCACTGCAACCTCTGCCTCCTGGATTCCAGCAGTTCTCCTGCCTCAACCTCCCGAGTAGCTGGG CTCACTGCAACCTCTGCCTCCTGGATTCCAGCGGTTCTCCTGCCTCAACCTCCCGAGTAGCTGGG T C DCAKD Ensembl:ENSG00000172992 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1186550210 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18699535 RMVar_hsa_circ_79331,RMVar_hsa_circ_184783,RMVar_hsa_circ_86883,RMVar_hsa_circ_184785 39520 RMVar_ID_39520 Human_SNP_ID_625319321 A-to-I Human chr17 - 45058276 45058276 45058276 CTGTCTCGCTCTGTCGCCTACGCTGGAGTGCAATGGCGCAATCTCGGCTTGCTGCAACCTCTGCC CTGTCTCGCTCTGTCGCCTACGCTGGAGTGCAGTGGCGCAATCTCGGCTTGCTGCAACCTCTGCC T C DCAKD Ensembl:ENSG00000172992 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs943856552 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2508757,Human_RBP_ID_13030302,Human_RBP_ID_17566513,Human_RBP_ID_23169909 RMVar_hsa_circ_79331,RMVar_hsa_circ_184783,RMVar_hsa_circ_86883,RMVar_hsa_circ_184785 39521 RMVar_ID_39521 Human_SNP_ID_625319915 A-to-I Human chr17 - 45060416 45060416 45060416 CAATCAAGGTATCCTCCCACCTCAGCCTCCCAAGTACCTAGGACTATAGGCATGAGCCACCACAC CAATCAAGGTATCCTCCCACCTCAGCCTCCCAGGTACCTAGGACTATAGGCATGAGCCACCACAC T C DCAKD Ensembl:ENSG00000172992 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025316229 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13030353 RMVar_hsa_circ_79331,RMVar_hsa_circ_184783,RMVar_hsa_circ_86883,RMVar_hsa_circ_184785 39522 RMVar_ID_39522 Human_SNP_ID_625321356 A-to-I Human chr17 + 45065912 45065912 45065912 TTTTTTTTTTTTTAAAGAGACTGTGTCTCGCTATGTTGCTCAGACTAGTCTCAAACTCCTGGGTT TTTTTTTTTTTTTAAAGAGACTGTGTCTCGCTGTGTTGCTCAGACTAGTCTCAAACTCCTGGGTT A G NMT1 Ensembl:ENSG00000136448 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1252235990 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25289610 RMVar_hsa_circ_92906,RMVar_hsa_circ_184789 39523 RMVar_ID_39523 Human_SNP_ID_625321376 A-to-I Human chr17 + 45065992 45065992 45065992 CCTTAGCCTCCCAAAGTGCTGGGATTGTAAGCATGAGCCACCACACCCAGCCTCCTGCCCCTTTT CCTTAGCCTCCCAAAGTGCTGGGATTGTAAGCGTGAGCCACCACACCCAGCCTCCTGCCCCTTTT A G NMT1 Ensembl:ENSG00000136448 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1186791097 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92906,RMVar_hsa_circ_184789 39524 RMVar_ID_39524 Human_SNP_ID_625321555 A-to-I Human chr17 + 45066770 45066770 45066770 AGGGCCTCGCTCTGTCGTCCAGGCTATAGTACAGTGGTGTGATCATGGCTTACTGCAGCCTTTGA AGGGCCTCGCTCTGTCGTCCAGGCTATAGTACGGTGGTGTGATCATGGCTTACTGCAGCCTTTGA A G NMT1 Ensembl:ENSG00000136448 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1457230525 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92906,RMVar_hsa_circ_184789 39525 RMVar_ID_39525 Human_SNP_ID_625322022 A-to-I Human chr17 + 45068724 45068724 45068724 GCTGGAGTACAGTGGCACGATCTTAGCTCACTACAACCTCTGCCTTACAGGTTCAAGCAATTCTT GCTGGAGTACAGTGGCACGATCTTAGCTCACTGCAACCTCTGCCTTACAGGTTCAAGCAATTCTT A G NMT1 Ensembl:ENSG00000136448 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1471302149 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92906,RMVar_hsa_circ_184789 39526 RMVar_ID_39526 Human_SNP_ID_625322902 A-to-I Human chr17 + 45072070 45072070 45072070 GTCCAGGAATTCAAGACCAGCCTGGGCAACATAGAGAAACTTTGTCTCTACAAAACATATAAAAA GTCCAGGAATTCAAGACCAGCCTGGGCAACATGGAGAAACTTTGTCTCTACAAAACATATAAAAA A G NMT1 Ensembl:ENSG00000136448 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1043080291 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92906,RMVar_hsa_circ_184789 39527 RMVar_ID_39527 Human_SNP_ID_625323015 A-to-I Human chr17 + 45072512 45072512 45072512 ATCTGAAACTCCTGACCTCAGCTGATCCACCCACCTTGGTCTCCCAAAGTGCTGGGATTACAGGT ATCTGAAACTCCTGACCTCAGCTGATCCACCCGCCTTGGTCTCCCAAAGTGCTGGGATTACAGGT A G NMT1 Ensembl:ENSG00000136448 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1271099199 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92906,RMVar_hsa_circ_184789 39528 RMVar_ID_39528 Human_SNP_ID_625323637 A-to-I Human chr17 + 45075069 45075069 45075069 ATGGTGGTGCACACCTGTAGCCCCAATTACTCAGGATGCTGAAGCAGGAGGATTGTTTGAGCCAG ATGGTGGTGCACACCTGTAGCCCCAATTACTCTGGATGCTGAAGCAGGAGGATTGTTTGAGCCAG A T NMT1 Ensembl:ENSG00000136448 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs990615269 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13030792 RMVar_hsa_circ_92906,RMVar_hsa_circ_184789 39529 RMVar_ID_39529 Human_SNP_ID_625325098 A-to-I Human chr17 + 45080822 45080822 45080822 GAGGTCTGTCTCTGTCATACAGGCTGGAGTGCAATGACGTGATCTCAACTCACTGCAACCTCCAC GAGGTCTGTCTCTGTCATACAGGCTGGAGTGCGATGACGTGATCTCAACTCACTGCAACCTCCAC A G NMT1 Ensembl:ENSG00000136448 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1386930178 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13030928 RMVar_hsa_circ_92906,RMVar_hsa_circ_184789 39530 RMVar_ID_39530 Human_SNP_ID_625325399 A-to-I Human chr17 + 45082131 45082131 45082131 ACAATGAAAGGCCCCCCCTTTCTTTTTGAGACAGAGTCTTACTCTGTTGCCCAGGCTAGAGTGTA ACAATGAAAGGCCCCCCCTTTCTTTTTGAGACGGAGTCTTACTCTGTTGCCCAGGCTAGAGTGTA A G NMT1 Ensembl:ENSG00000136448 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1488229222 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92906,RMVar_hsa_circ_62741,RMVar_hsa_circ_184789,RMVar_hsa_circ_271884,RMVar_hsa_circ_184790 39531 RMVar_ID_39531 Human_SNP_ID_625327315 A-to-I Human chr17 + 45090081 45090081 45090081 AAGGCAGGAGGATTGCTTGAGCCCAGCAGCTCAAGACCAGCCTGGACAACAGGGAAAGACCTCGT AAGGCAGGAGGATTGCTTGAGCCCAGCAGCTCGAGACCAGCCTGGACAACAGGGAAAGACCTCGT A G NMT1 Ensembl:ENSG00000136448 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1455115581 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92906,RMVar_hsa_circ_62741,RMVar_hsa_circ_184789,RMVar_hsa_circ_361836 39532 RMVar_ID_39532 Human_SNP_ID_625328666 A-to-I Human chr17 + 45095288 45095286 45095289 GTCACCACGCCAGGCTAATTTTTTTATTTTTTAGTAGAGATGGGGTTTCACCACATTGGCCAGGC GTCACCACGCCAGGCTAATTTTTTTATTTTT___TAGAGATGGGGTTTCACCACATTGGCCAGGC TTAG T NMT1 Ensembl:ENSG00000136448 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1311531011 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_16851,RMVar_hsa_circ_92906,RMVar_hsa_circ_62741,RMVar_hsa_circ_184789,RMVar_hsa_circ_361836,RMVar_hsa_circ_32978,RMVar_hsa_circ_30771 39533 RMVar_ID_39533 Human_SNP_ID_625328720 A-to-I Human chr17 + 45095511 45095511 45095511 GGTTGGGTGTGGTGGCTCACACCTGTAATTCCAACAATTTGGGAGTCTAAGGTGGGAAGATCGAT GGTTGGGTGTGGTGGCTCACACCTGTAATTCCGACAATTTGGGAGTCTAAGGTGGGAAGATCGAT A G NMT1 Ensembl:ENSG00000136448 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs539442193 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16851,RMVar_hsa_circ_92906,RMVar_hsa_circ_62741,RMVar_hsa_circ_184789,RMVar_hsa_circ_361836,RMVar_hsa_circ_32978,RMVar_hsa_circ_30771 39534 RMVar_ID_39534 Human_SNP_ID_625328779 A-to-I Human chr17 + 45095754 45095753 45095755 TGATCACACCAGTGCACTCCAGCCTGGGTAACAGAGTGAGACTCTATCTTGAAAAGAAAGGAAAA TGATCACACCAGTGCACTCCAGCCTGGGTAAC__AGTGAGACTCTATCTTGAAAAGAAAGGAAAA CAG C NMT1 Ensembl:ENSG00000136448 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1191528192 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_6600797 RMVar_hsa_circ_16851,RMVar_hsa_circ_92906,RMVar_hsa_circ_62741,RMVar_hsa_circ_184789,RMVar_hsa_circ_361836,RMVar_hsa_circ_32978,RMVar_hsa_circ_30771 39535 RMVar_ID_39535 Human_SNP_ID_625329791 A-to-I Human chr17 + 45100112 45100111 45100113 AGGTAGGGATTCTTTTTTTTTTGTTTTGAGACAGGGTCTCATTCTGTTGCCCAGGCTGGAGTGCA AGGTAGGGATTCTTTTTTTTTTGTTTTGAGAC__GGTCTCATTCTGTTGCCCAGGCTGGAGTGCA CAG C NMT1 Ensembl:ENSG00000136448 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1029819698 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_110318,RMVar_hsa_circ_184793 39536 RMVar_ID_39536 Human_SNP_ID_625329798 A-to-I Human chr17 + 45100163 45100163 45100163 CAGGCTGGAGTGCAGTGGCACAGTCACAGCTCACTGCAGCCTCGACCTCCCAGACTCAACTGATT CAGGCTGGAGTGCAGTGGCACAGTCACAGCTCGCTGCAGCCTCGACCTCCCAGACTCAACTGATT A G NMT1 Ensembl:ENSG00000136448 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1004661633 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110318,RMVar_hsa_circ_184793 39537 RMVar_ID_39537 Human_SNP_ID_625329915 A-to-I Human chr17 + 45100517 45100517 45100517 ATGGACCCGGGAGGTGGAGCTTGCAGTGAGCCAAGATCACGTCATTGCACTCCAGCCTAGGCGAC ATGGACCCGGGAGGTGGAGCTTGCAGTGAGCCGAGATCACGTCATTGCACTCCAGCCTAGGCGAC A G NMT1 Ensembl:ENSG00000136448 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1295826630 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23308330,Human_RBP_ID_25289736 RMVar_hsa_circ_110318,RMVar_hsa_circ_184793 39538 RMVar_ID_39538 Human_SNP_ID_625329926 A-to-I Human chr17 + 45100543 45100543 45100543 TGAGCCAAGATCACGTCATTGCACTCCAGCCTAGGCGACAGAGCGAGACTCCGTCTCAAAATAAA TGAGCCAAGATCACGTCATTGCACTCCAGCCTGGGCGACAGAGCGAGACTCCGTCTCAAAATAAA A G NMT1 Ensembl:ENSG00000136448 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1186661663 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110318,RMVar_hsa_circ_184793 39539 RMVar_ID_39539 Human_SNP_ID_625337595 A-to-I Human chr17 - 45126810 45126810 45126810 ACAAAAAAATTTAAAAATTATTCAGGCCTGGTAGTGCAAGTCTGTAGTCCCAGCTCCTCGGGAGG ACAAAAAAATTTAAAAATTATTCAGGCCTGGTGGTGCAAGTCTGTAGTCCCAGCTCCTCGGGAGG T C PLCD3 Ensembl:ENSG00000161714 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs899471173 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101263,RMVar_hsa_circ_184800 39540 RMVar_ID_39540 Human_SNP_ID_625341257 A-to-I Human chr17 + 45140563 45140563 45140563 AAAGTAGATTACAGGCCAGCGTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGA AAAGTAGATTACAGGCCAGCGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGA A G ACBD4 Ensembl:ENSG00000181513 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs544735006 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17565960 39541 RMVar_ID_39541 Human_SNP_ID_625341350 A-to-I Human chr17 + 45140965 45140965 45140965 AAACTGGCAGGCAGAGGTTGCAGTGAGCTGAGATGGTGCCATTGCACTCCAGCCTGAGCTACAGA AAACTGGCAGGCAGAGGTTGCAGTGAGCTGAGGTGGTGCCATTGCACTCCAGCCTGAGCTACAGA A G ACBD4 Ensembl:ENSG00000181513 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1366634416 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25289758 39542 RMVar_ID_39542 Human_SNP_ID_625341352 A-to-I Human chr17 + 45140978 45140978 45140978 GAGGTTGCAGTGAGCTGAGATGGTGCCATTGCACTCCAGCCTGAGCTACAGAGCAAGACTCCATC GAGGTTGCAGTGAGCTGAGATGGTGCCATTGCTCTCCAGCCTGAGCTACAGAGCAAGACTCCATC A T ACBD4 Ensembl:ENSG00000181513 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs781729260 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26782352 39543 RMVar_ID_39543 Human_SNP_ID_625341457 A-to-I Human chr17 + 45141506 45141506 45141506 GCCCAGGAGCTTGAGACCAGTCTGGGTAACATAGTGAGACCCTGTCTCCACAAAATATATGTTTA GCCCAGGAGCTTGAGACCAGTCTGGGTAACATGGTGAGACCCTGTCTCCACAAAATATATGTTTA A G ACBD4 Ensembl:ENSG00000181513 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1456899921 Functional Loss SNV dbSNP153 33..33 33 - - - 39544 RMVar_ID_39544 Human_SNP_ID_625341560 A-to-I Human chr17 + 45142129 45142129 45142129 AAGAAATTAATTTAGGCTGGGTACGGTGGCTCACGCCTGTAATCCTAGCACTTTGGGAGGCTGAG AAGAAATTAATTTAGGCTGGGTACGGTGGCTCCCGCCTGTAATCCTAGCACTTTGGGAGGCTGAG A C ACBD4 Ensembl:ENSG00000181513 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1401553199 Functional Loss SNV dbSNP153 33..33 33 - - - 39545 RMVar_ID_39545 Human_SNP_ID_625341564 A-to-I Human chr17 + 45142137 45142137 45142137 AATTTAGGCTGGGTACGGTGGCTCACGCCTGTAATCCTAGCACTTTGGGAGGCTGAGGTGGGTGG AATTTAGGCTGGGTACGGTGGCTCACGCCTGTGATCCTAGCACTTTGGGAGGCTGAGGTGGGTGG A G ACBD4 Ensembl:ENSG00000181513 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1339442235 Functional Loss SNV dbSNP153 33..33 33 - - - 39546 RMVar_ID_39546 Human_SNP_ID_625341746 A-to-I Human chr17 + 45142610 45142610 45142610 TGCAGTCTCACTCTGTCGGTCAGACTGGAGTGAAGTGGCGTGAACTCAGCTCACTGCAACCTCCG TGCAGTCTCACTCTGTCGGTCAGACTGGAGTGCAGTGGCGTGAACTCAGCTCACTGCAACCTCCG A C ACBD4 Ensembl:ENSG00000181513 Protein coding stop codon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1567909852 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1828090,Human_Splice_Rec_1828230 39547 RMVar_ID_39547 Human_SNP_ID_625341753 A-to-I Human chr17 + 45142635 45142635 45142635 TGGAGTGAAGTGGCGTGAACTCAGCTCACTGCAACCTCCGCCTCCCCGGGTTCAAGCAATTCTCT TGGAGTGAAGTGGCGTGAACTCAGCTCACTGCGACCTCCGCCTCCCCGGGTTCAAGCAATTCTCT A G ACBD4 Ensembl:ENSG00000181513 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs754499550 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1828090,Human_Splice_Rec_1828230 39548 RMVar_ID_39548 Human_SNP_ID_625341764 A-to-I Human chr17 + 45142660 45142660 45142660 TCACTGCAACCTCCGCCTCCCCGGGTTCAAGCAATTCTCTGCCTCAGCCTCCCGAGTAGCTGGGA TCACTGCAACCTCCGCCTCCCCGGGTTCAAGCTATTCTCTGCCTCAGCCTCCCGAGTAGCTGGGA A T ACBD4 Ensembl:ENSG00000181513 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,31158229,32596459 RNA-Seq:(High) rs923006811 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1828090,Human_Splice_Rec_1828230 39549 RMVar_ID_39549 Human_SNP_ID_625341808 A-to-I Human chr17 + 45142816 45142816 45142816 CCTGACCTCGTGACCACCTGCCTCGGCCTCCCAAAGTGCTGGGATGACAGGCGTGAGCCATCCCA CCTGACCTCGTGACCACCTGCCTCGGCCTCCCGAAGTGCTGGGATGACAGGCGTGAGCCATCCCA A G ACBD4 Ensembl:ENSG00000181513 Protein coding intron GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459,32596459 RNA-Seq:(High) rs539373311 Functional Loss SNV dbSNP153 33..33 33 - - - 39550 RMVar_ID_39550 Human_SNP_ID_625343683 A-to-I Human chr17 - 45148982 45148982 45148982 CAATCTGGGGAGCTCAAGTCAGTAAAGGGTTAAGCGCCCACAGTGCGGCCAGCTAGCGGGTCCAA CAATCTGGGGAGCTCAAGTCAGTAAAGGGTTAGGCGCCCACAGTGCGGCCAGCTAGCGGGTCCAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1323387795 Functional Loss SNV dbSNP153 33..33 33 - - - 39551 RMVar_ID_39551 Human_SNP_ID_625345146 A-to-I Human chr17 - 45153480 45153480 45153480 AAAAAAAAAGCCAGGCGCGGTGGCTTATGCCTATATTGCCAACACTTTGGGAGGCTGAGACGGGC AAAAAAAAAGCCAGGCGCGGTGGCTTATGCCTGTATTGCCAACACTTTGGGAGGCTGAGACGGGC T C AC138150.1 Ensembl:ENSG00000224505 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs886669589 Functional Loss SNV dbSNP153 33..33 33 - - - 39552 RMVar_ID_39552 Human_SNP_ID_625345395 A-to-I Human chr17 - 45154113 45154113 45154113 GAAGAAATAGGAGGCCGGGTGTGGTGGCTCACACCCATCATCCCAGCACTTTGGGAGGCCGAGGC GAAGAAATAGGAGGCCGGGTGTGGTGGCTCACGCCCATCATCCCAGCACTTTGGGAGGCCGAGGC T C AC138150.1 Ensembl:ENSG00000224505 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1240314998 Functional Loss SNV dbSNP153 33..33 33 - - - 39553 RMVar_ID_39553 Human_SNP_ID_625345986 A-to-I Human chr17 - 45156207 45156207 45156207 GCGATCTCGGCTCACTACAACCTCTGCCTCCCAGGTTCAAGCAATTGTCCTGCCTCAGCCTCCCG GCGATCTCGGCTCACTACAACCTCTGCCTCCCGGGTTCAAGCAATTGTCCTGCCTCAGCCTCCCG T C AC138150.1 Ensembl:ENSG00000224505 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1292246762 Functional Loss SNV dbSNP153 33..33 33 - - - 39554 RMVar_ID_39554 Human_SNP_ID_625346204 A-to-I Human chr17 - 45157057 45157057 45157057 TCCCTGCCTCAGCCTCCCAAATATCTGGGATTACAGGCGCCCACCACCACACCCGGCTAATTTTT TCCCTGCCTCAGCCTCCCAAATATCTGGGATTGCAGGCGCCCACCACCACACCCGGCTAATTTTT T C AC138150.1 Ensembl:ENSG00000224505 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1027847113 Functional Loss SNV dbSNP153 33..33 33 - - - 39555 RMVar_ID_39555 Human_SNP_ID_625346326 A-to-I Human chr17 - 45157504 45157501 45157505 AGCCACTGTGCCCGGCCTGTATTTGTATTTTTAGTAGAGACAGGGTTTTACCATGTTGGCCAGGC AGCCACTGTGCCCGGCCTGTATTTGTATTTT____AGAGACAGGGTTTTACCATGTTGGCCAGGC TACTA T AC138150.1 Ensembl:ENSG00000224505 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs780211951 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_5248011,Human_RBP_ID_13031695 39556 RMVar_ID_39556 Human_SNP_ID_625346407 A-to-I Human chr17 - 45157845 45157845 45157845 CCTCAGCCTCCCGCGTAGCTAGGATTACAGGCACTCACCACCATGCCTGGCTAATTTTTGCATTT CCTCAGCCTCCCGCGTAGCTAGGATTACAGGCGCTCACCACCATGCCTGGCTAATTTTTGCATTT T C AC138150.1 Ensembl:ENSG00000224505 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs906930871 Functional Loss SNV dbSNP153 33..33 33 - - - 39557 RMVar_ID_39557 Human_SNP_ID_625346409 A-to-I Human chr17 - 45157857 45157857 45157857 GCGATTCTCCTGCCTCAGCCTCCCGCGTAGCTAGGATTACAGGCACTCACCACCATGCCTGGCTA GCGATTCTCCTGCCTCAGCCTCCCGCGTAGCTGGGATTACAGGCACTCACCACCATGCCTGGCTA T C AC138150.1 Ensembl:ENSG00000224505 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1186730993 Functional Loss SNV dbSNP153 33..33 33 - - - 39558 RMVar_ID_39558 Human_SNP_ID_625346734 A-to-I Human chr17 - 45158882 45158882 45158882 AAAATTAGCTGAGTGTGGTGGTGTGCACCTGTAGTCACAGCTACTTGGGAAGCTGAGGCAGGAGA AAAATTAGCTGAGTGTGGTGGTGTGCACCTGTGGTCACAGCTACTTGGGAAGCTGAGGCAGGAGA T C AC138150.1 Ensembl:ENSG00000224505 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1393456299 Functional Loss SNV dbSNP153 33..33 33 - - - 39559 RMVar_ID_39559 Human_SNP_ID_625346940 A-to-I Human chr17 - 45159674 45159674 45159674 GGGAGGCTGAGGCAGGAGAATCGCTTGAACCCAGGAGGCAGAGTTTGCCATGAGCCTCTCACCGT GGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGGGAGGCAGAGTTTGCCATGAGCCTCTCACCGT T C AC138150.1 Ensembl:ENSG00000224505 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs563959182 Functional Loss SNV dbSNP153 33..33 33 - - - 39560 RMVar_ID_39560 Human_SNP_ID_625362265 A-to-I Human chr17 - 45217247 45217247 45217247 GGTGTGTGCCACCACGTTCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGG GGTGTGTGCCACCACGTTCAGCTAATTTTTGTGTTTTTAGTAGAGACGGGGTTTCACCATGTTGG T C AC008105.3 Ensembl:ENSG00000267121 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1244314161 Functional Loss SNV dbSNP153 33..33 33 - - - 39561 RMVar_ID_39561 Human_SNP_ID_625362267 A-to-I Human chr17 - 45217256 45217256 45217256 GGGACTACAGGTGTGTGCCACCACGTTCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCA GGGACTACAGGTGTGTGCCACCACGTTCAGCTGATTTTTGTATTTTTAGTAGAGACGGGGTTTCA T C AC008105.3 Ensembl:ENSG00000267121 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1275164815 Functional Loss SNV dbSNP153 33..33 33 - - - 39562 RMVar_ID_39562 Human_SNP_ID_625362296 A-to-I Human chr17 - 45217371 45217371 45217371 ACAGAGTCTCACTCTGTTGCCCAGGCGGCTGGAGTGCAGTGGTGTGATCTCAGCTCACTGCGACC ACAGAGTCTCACTCTGTTGCCCAGGCGGCTGGGGTGCAGTGGTGTGATCTCAGCTCACTGCGACC T C AC008105.3 Ensembl:ENSG00000267121 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs539539349 Functional Loss SNV dbSNP153 33..33 33 - - - 39563 RMVar_ID_39563 Human_SNP_ID_625362310 A-to-I Human chr17 - 45217401 45217401 45217401 TTTTTTGTTTTTGTTTTTGTTTTTTTTTAGACAGAGTCTCACTCTGTTGCCCAGGCGGCTGGAGT TTTTTTGTTTTTGTTTTTGTTTTTTTTTAGACGGAGTCTCACTCTGTTGCCCAGGCGGCTGGAGT T C AC008105.3 Ensembl:ENSG00000267121 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs945902365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13031771 39564 RMVar_ID_39564 Human_SNP_ID_625362501 A-to-I Human chr17 - 45217631 45217576 45217632 TTGAACTTGGGAGGCGGAGGGTGCCGCGAGCCAAGATCACGCCAGTGCACTCTAGCCTGGGCAAC TTGAACTTGGGAGGCGGAGGGTGCCGCGAGC__________________________________ CCTTCGAGATGGAGTCTTGCTCTGTTGCCCAGGCTAGAGTGCACTGGCGTGATCTTG C AC008105.3 Ensembl:ENSG00000267121 lincRNA intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1567948025 Functional Loss DEL dbSNP153 32..65 33 - - - 39565 RMVar_ID_39565 Human_SNP_ID_625362592 A-to-I Human chr17 - 45217700 45217700 45217700 AAATTAGCTTGGCGTAGTGGCGGGTGCCTGTAATCCCAGGTACTCGGGAGGCTGAGGCAGGAGAA AAATTAGCTTGGCGTAGTGGCGGGTGCCTGTAGTCCCAGGTACTCGGGAGGCTGAGGCAGGAGAA T C AC008105.3 Ensembl:ENSG00000267121 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1225204213 Functional Loss SNV dbSNP153 33..33 33 - - - 39566 RMVar_ID_39566 Human_SNP_ID_625362602 A-to-I Human chr17 - 45217745 45217739 45217746 CAGCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATATAAAAATTAGCTTGGCGTAGTGG CAGCCTGGCCAACATGGTGAAACCCCGTCTC_______AATATAAAAATTAGCTTGGCGTAGTGG TTTTAGTA T AC008105.3 Ensembl:ENSG00000267121 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1358291646 Functional Loss DEL dbSNP153 32..38 33 - - - 39567 RMVar_ID_39567 Human_SNP_ID_625362629 A-to-I Human chr17 - 45217857 45217857 45217857 ATGTGCAAAGAAAGTAAAGTCCCTCCTGGCCAAGTGCGATGGCTCAAGCCTGTAATCTCAACACC ATGTGCAAAGAAAGTAAAGTCCCTCCTGGCCAGGTGCGATGGCTCAAGCCTGTAATCTCAACACC T C AC008105.3 Ensembl:ENSG00000267121 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs989936564 Functional Loss SNV dbSNP153 33..33 33 - - - 39568 RMVar_ID_39568 Human_SNP_ID_625362805 A-to-I Human chr17 - 45218235 45218235 45218235 AAAAAAAAAGAAAAAGGGGCCAGGCACCTGTAATCCCAGCACTTTGGGAGGCTGAGGAGGGAAGA AAAAAAAAAGAAAAAGGGGCCAGGCACCTGTATTCCCAGCACTTTGGGAGGCTGAGGAGGGAAGA T A AC008105.3 Ensembl:ENSG00000267121 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs902553760 Functional Loss SNV dbSNP153 33..33 33 - - - 39569 RMVar_ID_39569 Human_SNP_ID_625362875 A-to-I Human chr17 - 45218399 45218399 45218399 AAATTAGCCGGGTGTGGTGGCGCATGCCTGTAATCCTAGCTACTCGGGAGGCCGAGGCAGGAGAA AAATTAGCCGGGTGTGGTGGCGCATGCCTGTAGTCCTAGCTACTCGGGAGGCCGAGGCAGGAGAA T C AC008105.3 Ensembl:ENSG00000267121 lincRNA intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1219590082 Functional Loss SNV dbSNP153 33..33 33 - - - 39570 RMVar_ID_39570 Human_SNP_ID_625362915 A-to-I Human chr17 - 45218542 45218542 45218542 AAAAAGGAAAAAGGGGCCGGGCGCGGTGGCTCACGTCTATAATCCTAGCACTTTGGGAGACCAAG AAAAAGGAAAAAGGGGCCGGGCGCGGTGGCTCTCGTCTATAATCCTAGCACTTTGGGAGACCAAG T A AC008105.3 Ensembl:ENSG00000267121 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1289911228 Functional Loss SNV dbSNP153 33..33 33 - - - 39571 RMVar_ID_39571 Human_SNP_ID_625363268 A-to-I Human chr17 - 45220002 45220002 45220002 CAGGCTGGAGTGCAGTGGCTCGGTCTCAGCTCACTGCAACCTCCACCTCCCAGGTCCAAGCAATT CAGGCTGGAGTGCAGTGGCTCGGTCTCAGCTCGCTGCAACCTCCACCTCCCAGGTCCAAGCAATT T C AC008105.3 Ensembl:ENSG00000267121 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1018930330 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1828334 39572 RMVar_ID_39572 Human_SNP_ID_625363269 A-to-I Human chr17 - 45220007 45220007 45220007 TTGCCCAGGCTGGAGTGCAGTGGCTCGGTCTCAGCTCACTGCAACCTCCACCTCCCAGGTCCAAG TTGCCCAGGCTGGAGTGCAGTGGCTCGGTCTCGGCTCACTGCAACCTCCACCTCCCAGGTCCAAG T C AC008105.3 Ensembl:ENSG00000267121 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1194223260 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1828334 39573 RMVar_ID_39573 Human_SNP_ID_625371515 A-to-I Human chr17 + 45251023 45251023 45251023 CCCTCTATGCAGGGGATTCTGGGGAAAGGGGTAGGGCAGTGATTCCCCCCACCCTGGGTGAGGGA CCCTCTATGCAGGGGATTCTGGGGAAAGGGGTGGGGCAGTGATTCCCCCCACCCTGGGTGAGGGA A G MAP3K14-AS1 Ensembl:ENSG00000267278 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1343135831 Functional Loss SNV dbSNP153 33..33 33 - - - 39574 RMVar_ID_39574 Human_SNP_ID_625371516 A-to-I Human chr17 + 45251023 45251023 45251023 CCCTCTATGCAGGGGATTCTGGGGAAAGGGGTAGGGCAGTGATTCCCCCCACCCTGGGTGAGGGA CCCTCTATGCAGGGGATTCTGGGGAAAGGGGTTGGGCAGTGATTCCCCCCACCCTGGGTGAGGGA A T MAP3K14-AS1 Ensembl:ENSG00000267278 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1343135831 Functional Loss SNV dbSNP153 33..33 33 - - - 39575 RMVar_ID_39575 Human_SNP_ID_625376861 A-to-I Human chr17 - 45272214 45272214 45272214 TCAAGCGATCCTCCCACCTCAGCCTCCTGAGTAGCTGGGACCACAGCATGTACCACCATGTCCGG TCAAGCGATCCTCCCACCTCAGCCTCCTGAGTGGCTGGGACCACAGCATGTACCACCATGTCCGG T C MAP3K14 Ensembl:ENSG00000006062 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1158670981 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41234 39576 RMVar_ID_39576 Human_SNP_ID_625376997 A-to-I Human chr17 - 45272896 45272896 45272896 TCACTCTGTCACCCAGGCTGGAGTGCAGTGGCACAATCTCAGCTCACTGCAACCTCCTCCTCCCG TCACTCTGTCACCCAGGCTGGAGTGCAGTGGCGCAATCTCAGCTCACTGCAACCTCCTCCTCCCG T C MAP3K14 Ensembl:ENSG00000006062 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs972424167 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41234 39577 RMVar_ID_39577 Human_SNP_ID_625377673 A-to-I Human chr17 - 45275275 45275275 45275275 TTAGTAGAGACAGGGTTTCGCCATGTTGGCCAAGATGGTCTTGATCTCCCGACCTCGATCTCCTT TTAGTAGAGACAGGGTTTCGCCATGTTGGCCAGGATGGTCTTGATCTCCCGACCTCGATCTCCTT T C MAP3K14 Ensembl:ENSG00000006062 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs36107645 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11822,RMVar_hsa_circ_29831,RMVar_hsa_circ_27741 39578 RMVar_ID_39578 Human_SNP_ID_625377899 A-to-I Human chr17 - 45275926 45275926 45275926 AAACCCCGTCTCTACTAAAAAATACAAAAATTATCTGGGCCTGGTGGCGCACACTTGTAGTCCCA AAACCCCGTCTCTACTAAAAAATACAAAAATTGTCTGGGCCTGGTGGCGCACACTTGTAGTCCCA T C MAP3K14 Ensembl:ENSG00000006062 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1374457376 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11822,RMVar_hsa_circ_29831,RMVar_hsa_circ_27741 39579 RMVar_ID_39579 Human_SNP_ID_625377903 A-to-I Human chr17 - 45275945 45275945 45275945 CAGCCTGGCCAGCATGGTGAAACCCCGTCTCTACTAAAAAATACAAAAATTATCTGGGCCTGGTG CAGCCTGGCCAGCATGGTGAAACCCCGTCTCTGCTAAAAAATACAAAAATTATCTGGGCCTGGTG T C MAP3K14 Ensembl:ENSG00000006062 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs779306975 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11822,RMVar_hsa_circ_29831,RMVar_hsa_circ_27741 39580 RMVar_ID_39580 Human_SNP_ID_625377904 A-to-I Human chr17 - 45275945 45275945 45275945 CAGCCTGGCCAGCATGGTGAAACCCCGTCTCTACTAAAAAATACAAAAATTATCTGGGCCTGGTG CAGCCTGGCCAGCATGGTGAAACCCCGTCTCTCCTAAAAAATACAAAAATTATCTGGGCCTGGTG T G MAP3K14 Ensembl:ENSG00000006062 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs779306975 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11822,RMVar_hsa_circ_29831,RMVar_hsa_circ_27741 39581 RMVar_ID_39581 Human_SNP_ID_625379174 A-to-I Human chr17 - 45281157 45281157 45281157 AGGAAGTAGAGGCTGCAGTGAGCCAAGATCGTACCACTGCACTCCAGCCTGGACAACAGAGTGAG AGGAAGTAGAGGCTGCAGTGAGCCAAGATCGTGCCACTGCACTCCAGCCTGGACAACAGAGTGAG T C MAP3K14 Ensembl:ENSG00000006062 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1337095713 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11822,RMVar_hsa_circ_29831,RMVar_hsa_circ_27741 39582 RMVar_ID_39582 Human_SNP_ID_625379457 A-to-I Human chr17 - 45282218 45282213 45282219 GCATAAAAAGTCCAGGCTGGGTACAGTGGCTCACGCTTGTAATCCCAGTACTTTGGGAGGCTGAG GCATAAAAAGTCCAGGCTGGGTACAGTGGCT______TGTAATCCCAGTACTTTGGGAGGCTGAG AAGCGTG A MAP3K14 Ensembl:ENSG00000006062 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1454421885 Functional Loss DEL dbSNP153 32..37 33 - - - RMVar_hsa_circ_11822,RMVar_hsa_circ_29831,RMVar_hsa_circ_27741 39583 RMVar_ID_39583 Human_SNP_ID_625379497 A-to-I Human chr17 - 45282390 45282390 45282390 CCACCACACCCAGCTAATTTTTTATTTTTTGTAGAAACAGGATCTCACTATGTTGCCCAGGCTGG CCACCACACCCAGCTAATTTTTTATTTTTTGTGGAAACAGGATCTCACTATGTTGCCCAGGCTGG T C MAP3K14 Ensembl:ENSG00000006062 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1307687139 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11822,RMVar_hsa_circ_29831,RMVar_hsa_circ_27741 39584 RMVar_ID_39584 Human_SNP_ID_625383690 A-to-I Human chr17 - 45301081 45301081 45301081 TCACTGCAACCTTGCACTCCTAGACTAAAGCAATCCTTCCACCTCAGCCTCCTGAGTAGCTAGAA TCACTGCAACCTTGCACTCCTAGACTAAAGCAGTCCTTCCACCTCAGCCTCCTGAGTAGCTAGAA T C MAP3K14 Ensembl:ENSG00000006062 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1252682483 Functional Loss SNV dbSNP153 33..33 33 - - - 39585 RMVar_ID_39585 Human_SNP_ID_625384782 A-to-I Human chr17 - 45305534 45305534 45305534 GAAATTAGCCATGCGTGGTGGTACATGCCTGTAATCCCAGCCACTTGGGTGGCTGAGGCATAAGA GAAATTAGCCATGCGTGGTGGTACATGCCTGTTATCCCAGCCACTTGGGTGGCTGAGGCATAAGA T A MAP3K14 Ensembl:ENSG00000006062 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1001456775 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24372780 39586 RMVar_ID_39586 Human_SNP_ID_625415937 A-to-I Human chr17 - 45434078 45434078 45434078 TGTCGCCCAGGCTGAAGTGCAGTGGCACGATCATGGCTCACGGCAGTCTCCGCCTCCCAGGTTCA TGTCGCCCAGGCTGAAGTGCAGTGGCACGATCCTGGCTCACGGCAGTCTCCGCCTCCCAGGTTCA T G ARHGAP27 Ensembl:ENSG00000159314 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1329485265 Functional Loss SNV dbSNP153 33..33 33 - - - 39587 RMVar_ID_39587 Human_SNP_ID_625461267 A-to-I Human chr17 + 45631822 45631822 45631822 AAAATTAGCCGGGTACGGTAGCGGGCGCCTGTAGTCCCAGCTGCTCGGGAGGCTGAGGCAGGAGA AAAATTAGCCGGGTACGGTAGCGGGCGCCTGTGGTCCCAGCTGCTCGGGAGGCTGAGGCAGGAGA A G LINC02210-CRHR1,LINC02210 Ensembl:ENSG00000263715,Ensembl:ENSG00000204650 Protein coding,Pseudogene intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs545394136 Functional Loss SNV dbSNP153 33..33 33 - - - 39588 RMVar_ID_39588 Human_SNP_ID_625462896 A-to-I Human chr17 + 45638955 45638955 45638955 GTGCAATGGTGTGATCTCTGCCTCCTGGGTTCAAGCGATTCTCCTGCCTCAAGCTCCTGAGTAGC GTGCAATGGTGTGATCTCTGCCTCCTGGGTTCCAGCGATTCTCCTGCCTCAAGCTCCTGAGTAGC A C LINC02210-CRHR1,LINC02210 Ensembl:ENSG00000263715,Ensembl:ENSG00000204650 Protein coding,Pseudogene intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886701157 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17379941,Human_RBP_ID_18297729,Human_RBP_ID_25290212 39589 RMVar_ID_39589 Human_SNP_ID_625462932 A-to-I Human chr17 + 45639115 45639113 45639115 TGACCTCATGATCCGCCTGCCTCGGCCTCCCAAAGTGTTGGGATTACAGGTGTGAGCCACCGCAC TGACCTCATGATCCGCCTGCCTCGGCCTCCC__AGTGTTGGGATTACAGGTGTGAGCCACCGCAC CAA C LINC02210-CRHR1,LINC02210 Ensembl:ENSG00000263715,Ensembl:ENSG00000204650 Protein coding,Pseudogene intron,intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1321259104 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_132714,Human_RBP_ID_1091527,Human_RBP_ID_9883119,Human_RBP_ID_17495237,Human_RBP_ID_25342862 39590 RMVar_ID_39590 Human_SNP_ID_625463148 A-to-I Human chr17 + 45640032 45640032 45640032 CACCACATCTGGCTAATTTTTGTATGAGTAGTAGAGACGGGGATGCACTATGTTGGCCAGGCTGG CACCACATCTGGCTAATTTTTGTATGAGTAGTGGAGACGGGGATGCACTATGTTGGCCAGGCTGG A G LINC02210-CRHR1,LINC02210 Ensembl:ENSG00000263715,Ensembl:ENSG00000204650 Protein coding,Pseudogene intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1176320886 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6601449,Human_RBP_ID_13033224 39591 RMVar_ID_39591 Human_SNP_ID_625463373 A-to-I Human chr17 + 45640957 45640943 45640957 AAAATTAGCCAGGTGTGGTGGTGCACGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGAAGGAGA AAAATTAGCCAGGTGTGGT______________GTCCCAGCTACTTGGGAGGCTGAGGAAGGAGA TGGTGCACGCCTGTA T LINC02210-CRHR1,LINC02210 Ensembl:ENSG00000263715,Ensembl:ENSG00000204650 Protein coding,Pseudogene intron,intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1307939935 Functional Loss DEL dbSNP153 20..33 33 - - - Human_RBP_ID_9883121 39592 RMVar_ID_39592 Human_SNP_ID_625463387 A-to-I Human chr17 + 45640983 45640983 45640983 GCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGAAGGAGAATCACTTGAACCTGGGAGGTGGAGGC GCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGTAGGAGAATCACTTGAACCTGGGAGGTGGAGGC A T LINC02210-CRHR1,LINC02210 Ensembl:ENSG00000263715,Ensembl:ENSG00000204650 Protein coding,Pseudogene intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1471264741 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9883121 39593 RMVar_ID_39593 Human_SNP_ID_625463494 A-to-I Human chr17 + 45641458 45641458 45641458 GTGAGATGAGACTGAGCCATTGCACTCAGCCTAGGCAACAGAGTGAGACCCTGTCTCAAAACAAA GTGAGATGAGACTGAGCCATTGCACTCAGCCTGGGCAACAGAGTGAGACCCTGTCTCAAAACAAA A G LINC02210-CRHR1,LINC02210 Ensembl:ENSG00000263715,Ensembl:ENSG00000204650 Protein coding,Pseudogene intron,intron GSE38233;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,32596459 RNA-Seq:(High) rs1322230806 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_132719,Human_RBP_ID_1286810,Human_RBP_ID_9883343,Human_RBP_ID_13033272,Human_RBP_ID_17673413,Human_RBP_ID_23729694 39594 RMVar_ID_39594 Human_SNP_ID_625464109 A-to-I Human chr17 + 45643471 45643471 45643471 TTGGCTCACTGCAACCTCCGCCTCCTGAGTTCAAGTGATTCTCCTGCCTCAGCCTCCTGAGTATT TTGGCTCACTGCAACCTCCGCCTCCTGAGTTCCAGTGATTCTCCTGCCTCAGCCTCCTGAGTATT A C LINC02210-CRHR1,LINC02210 Ensembl:ENSG00000263715,Ensembl:ENSG00000204650 Protein coding,Pseudogene intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs911125976 Functional Loss SNV dbSNP153 33..33 33 - - - 39595 RMVar_ID_39595 Human_SNP_ID_625464315 A-to-I Human chr17 + 45644240 45644240 45644240 CCAGCTACTTGGGAGGCTGAGAAATGAGAATCACTTGAACCCAGGAGGTGGAGGCTACAGTGAGC CCAGCTACTTGGGAGGCTGAGAAATGAGAATCGCTTGAACCCAGGAGGTGGAGGCTACAGTGAGC A G LINC02210-CRHR1,LINC02210 Ensembl:ENSG00000263715,Ensembl:ENSG00000204650 Protein coding,Pseudogene intron,intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1485737822 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8254059,Human_RBP_ID_17379087,Human_RBP_ID_18514388 39596 RMVar_ID_39596 Human_SNP_ID_625464495 A-to-I Human chr17 + 45644989 45644989 45644989 GAAACCCCATCTCTACCCAAAATACAAAAATTAGCTGGGTGTGGTGGCACCCACCTGTAGTCCCA GAAACCCCATCTCTACCCAAAATACAAAAATTGGCTGGGTGTGGTGGCACCCACCTGTAGTCCCA A G LINC02210-CRHR1,LINC02210 Ensembl:ENSG00000263715,Ensembl:ENSG00000204650 Protein coding,Pseudogene intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs966831178 Functional Loss SNV dbSNP153 33..33 33 - - - 39597 RMVar_ID_39597 Human_SNP_ID_625530105 A-to-I Human chr17 + 45914833 45914833 45914833 GCCTGAACCTCCCAGGCTCAAGCAATCCTCCCACCTCAGCCTCCTGAGTAGCTGGGACTATAGGC GCCTGAACCTCCCAGGCTCAAGCAATCCTCCCGCCTCAGCCTCCTGAGTAGCTGGGACTATAGGC A G MAPT Ensembl:ENSG00000186868 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1169985880 Functional Loss SNV dbSNP153 33..33 33 - - - 39598 RMVar_ID_39598 Human_SNP_ID_625555019 A-to-I Human chr17 + 46016263 46016263 46016263 AAAATACAAAAACTAGCCAGGCATGGTGGCACATGCCTGTAATCCCAGCTACTTGGGAGGCTGAA AAAATACAAAAACTAGCCAGGCATGGTGGCACGTGCCTGTAATCCCAGCTACTTGGGAGGCTGAA A G MAPT Ensembl:ENSG00000186868 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs146232566 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267428,RMVar_hsa_circ_265713 39599 RMVar_ID_39599 Human_SNP_ID_625555022 A-to-I Human chr17 + 46016281 46016281 46016281 AGGCATGGTGGCACATGCCTGTAATCCCAGCTACTTGGGAGGCTGAAGCAGGAGAATCACTTGAA AGGCATGGTGGCACATGCCTGTAATCCCAGCTGCTTGGGAGGCTGAAGCAGGAGAATCACTTGAA A G MAPT Ensembl:ENSG00000186868 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1394451479 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267428,RMVar_hsa_circ_265713 39600 RMVar_ID_39600 Human_SNP_ID_625562442 A-to-I Human chr17 - 46044213 46044213 46044213 ACCTGATAAGGATCAGCACCCTCTTCTCTGAAAATAGCAGTTTACCTATGTGGGTATGGAATGTA ACCTGATAAGGATCAGCACCCTCTTCTCTGAAGATAGCAGTTTACCTATGTGGGTATGGAATGTA T C KANSL1 Ensembl:ENSG00000120071 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs72836318 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8454467,Human_RBP_ID_13034518 GWAS_ID_4678,GWAS_ID_4679 RMVar_hsa_circ_81639,RMVar_hsa_circ_107285,RMVar_hsa_circ_184831,RMVar_hsa_circ_184832,RMVar_hsa_circ_122187,RMVar_hsa_circ_184834 39601 RMVar_ID_39601 Human_SNP_ID_625563350 A-to-I Human chr17 - 46047543 46047543 46047543 AGCTCAAGTGATCCACCCATCTTGGCCTCTCAAAGTGCTGGGATTACAGGTGTAAACCACCACGC AGCTCAAGTGATCCACCCATCTTGGCCTCTCAGAGTGCTGGGATTACAGGTGTAAACCACCACGC T C KANSL1 Ensembl:ENSG00000120071 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1222016323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25290400 RMVar_hsa_circ_81639,RMVar_hsa_circ_107285,RMVar_hsa_circ_184831,RMVar_hsa_circ_184832,RMVar_hsa_circ_122187,RMVar_hsa_circ_184834 39602 RMVar_ID_39602 Human_SNP_ID_625563367 A-to-I Human chr17 - 46047599 46047599 46047599 TCCCGCCCCCTACAAAGATGGGGTCTTGCTATATTGCCCAGGCTGGTTTTGAACTGAGCTCAAGT TCCCGCCCCCTACAAAGATGGGGTCTTGCTATGTTGCCCAGGCTGGTTTTGAACTGAGCTCAAGT T C KANSL1 Ensembl:ENSG00000120071 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1359943278 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81639,RMVar_hsa_circ_107285,RMVar_hsa_circ_184831,RMVar_hsa_circ_184832,RMVar_hsa_circ_122187,RMVar_hsa_circ_184834 39603 RMVar_ID_39603 Human_SNP_ID_625563403 A-to-I Human chr17 - 46047725 46047725 46047725 GGAGTTCAGTGGAGTGATCACAGCTCACTGCAACCTTGACTTCCTGGGCTCTAAACAGTCCTCCC GGAGTTCAGTGGAGTGATCACAGCTCACTGCAGCCTTGACTTCCTGGGCTCTAAACAGTCCTCCC T C KANSL1 Ensembl:ENSG00000120071 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053006602 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81639,RMVar_hsa_circ_107285,RMVar_hsa_circ_184831,RMVar_hsa_circ_184832,RMVar_hsa_circ_122187,RMVar_hsa_circ_184834 39604 RMVar_ID_39604 Human_SNP_ID_625563576 A-to-I Human chr17 - 46048111 46048111 46048111 CTGAGGTCAGAAGTTTGAGACCAGCATGGGCAACATGGCAAAACCCTATCTCTACTAAAAACACA CTGAGGTCAGAAGTTTGAGACCAGCATGGGCAGCATGGCAAAACCCTATCTCTACTAAAAACACA T C KANSL1 Ensembl:ENSG00000120071 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs900945849 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81639,RMVar_hsa_circ_107285,RMVar_hsa_circ_184831,RMVar_hsa_circ_184832,RMVar_hsa_circ_122187,RMVar_hsa_circ_184834 39605 RMVar_ID_39605 Human_SNP_ID_625567807 A-to-I Human chr17 - 46062487 46062487 46062487 GGGCGTGGTGGCACGTGCCTGTAATCCCAGCTACTCGAGAGGCTGGGGCAGGAGAATCGCTTGAA GGGCGTGGTGGCACGTGCCTGTAATCCCAGCTGCTCGAGAGGCTGGGGCAGGAGAATCGCTTGAA T C KANSL1 Ensembl:ENSG00000120071 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs919260044 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 39606 RMVar_ID_39606 Human_SNP_ID_625569705 A-to-I Human chr17 - 46069488 46069488 46069488 TGCCTGCTTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCACACCCAGCCTCAGTCT TGCCTGCTTCAGCCTCCCAAAGTGCTGGGATTGCAGGCATGAGCCACCACACCCAGCCTCAGTCT T C KANSL1 Ensembl:ENSG00000120071 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1380911817 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_184843,RMVar_hsa_circ_184837,RMVar_hsa_circ_184838,RMVar_hsa_circ_184839,RMVar_hsa_circ_372349,RMVar_hsa_circ_372399,RMVar_hsa_circ_117725,RMVar_hsa_circ_81875,RMVar_hsa_circ_184841,RMVar_hsa_circ_184842,RMVar_hsa_circ_184844 39607 RMVar_ID_39607 Human_SNP_ID_625574281 A-to-I Human chr17 - 46086994 46086994 46086994 GGAGGCCAGGGCGGGTAGATCTCTTGGCCCCAAGAGTTTGCAACCAGCCTTGGCAACATGGTGAA GGAGGCCAGGGCGGGTAGATCTCTTGGCCCCACGAGTTTGCAACCAGCCTTGGCAACATGGTGAA T G KANSL1 Ensembl:ENSG00000120071 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1329238570 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81639,RMVar_hsa_circ_184831,RMVar_hsa_circ_378857,RMVar_hsa_circ_123012,RMVar_hsa_circ_71139,RMVar_hsa_circ_184843,RMVar_hsa_circ_184838,RMVar_hsa_circ_184839,RMVar_hsa_circ_372349,RMVar_hsa_circ_117725,RMVar_hsa_circ_81875,RMVar_hsa_circ_184842,RMVar_hsa_circ_364864,RMVar_hsa_circ_184844,RMVar_hsa_circ_126756,RMVar_hsa_circ_184845,RMVar_hsa_circ_184846 39608 RMVar_ID_39608 Human_SNP_ID_625578527 A-to-I Human chr17 - 46102523 46102523 46102523 CTCTGGGGCTGGGTGCTGTGGCTCACACCTGTAACTGCAGCACTTTGGGAGGCTGAGGCAGACGG CTCTGGGGCTGGGTGCTGTGGCTCACACCTGTTACTGCAGCACTTTGGGAGGCTGAGGCAGACGG T A KANSL1 Ensembl:ENSG00000120071 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs556025423 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_236027,Human_RBP_ID_6602183,Human_RBP_ID_25290740 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 39609 RMVar_ID_39609 Human_SNP_ID_625586839 A-to-I Human chr17 - 46132942 46132942 46132942 AGGTTTCCATCTGCTTACTTTTGTTTTTTTCGAGACACGGTCTTGCTGTGTCGCCCAAGCTGGAA AGGTTTCCATCTGCTTACTTTTGTTTTTTTCGTGACACGGTCTTGCTGTGTCGCCCAAGCTGGAA T A KANSL1 Ensembl:ENSG00000120071 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1342821368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2509264,Human_RBP_ID_6602503,Human_RBP_ID_13036956 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 39610 RMVar_ID_39610 Human_SNP_ID_625589625 A-to-I Human chr17 - 46142557 46142557 46142557 TTGCCCAGGCTAGAGTGCAGTGGCATAGTCGTAGCTTGCTGCAGCTTCAACCTCCAGGACTCAAG TTGCCCAGGCTAGAGTGCAGTGGCATAGTCGTGGCTTGCTGCAGCTTCAACCTCCAGGACTCAAG T C KANSL1 Ensembl:ENSG00000120071 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1004279722 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9863583,Human_RBP_ID_23730091 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 39611 RMVar_ID_39611 Human_SNP_ID_625591104 A-to-I Human chr17 - 46147417 46147417 46147417 GGCGCATGCTACCACATCTGGCTAATTTTTGTATTTTTTGTAGAGACAGGATCTTGCCACCTTGC GGCGCATGCTACCACATCTGGCTAATTTTTGTGTTTTTTGTAGAGACAGGATCTTGCCACCTTGC T C KANSL1 Ensembl:ENSG00000120071 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1400265584 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2509358,Human_RBP_ID_13037822 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 39612 RMVar_ID_39612 Human_SNP_ID_625591576 A-to-I Human chr17 - 46148711 46148711 46148711 AAGGCATGGTGGGTGCTTGTACCCAGCTGTTCAGGAGGCTGAGGCAGGAGAATCAATTGAACCCA AAGGCATGGTGGGTGCTTGTACCCAGCTGTTCGGGAGGCTGAGGCAGGAGAATCAATTGAACCCA T C KANSL1 Ensembl:ENSG00000120071 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1458345179 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13037892 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 39613 RMVar_ID_39613 Human_SNP_ID_625593975 A-to-I Human chr17 - 46156893 46156893 46156893 TGTGACTGATTTTTTTTTTTTTTTTTGGAGATAGAGTCTCACTCTGTCACCCAGGCTGGCGTACA TGTGACTGATTTTTTTTTTTTTTTTTGGAGATGGAGTCTCACTCTGTCACCCAGGCTGGCGTACA T C KANSL1 Ensembl:ENSG00000120071 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs372215531 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13038307 Human_Splice_Rec_1830286 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 39614 RMVar_ID_39614 Human_SNP_ID_625594947 A-to-I Human chr17 - 46160460 46160460 46160460 GCGAAACCCCTTCTCTACAAAAAAAAGTAGCCAGGCGTGGTGGCATGCGCCTATAGTCCCAGCTT GCGAAACCCCTTCTCTACAAAAAAAAGTAGCCGGGCGTGGTGGCATGCGCCTATAGTCCCAGCTT T C KANSL1 Ensembl:ENSG00000120071 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1347768001 Functional Loss SNV dbSNP153 33..33 33 - - - 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 39615 RMVar_ID_39615 Human_SNP_ID_625596147 A-to-I Human chr17 - 46165031 46165031 46165031 GTGATGTCAGCTCATTGCAGTCTCTGCTTCCCAGGTTCAAGTGATCTTCCTGCCTCAGCCTCAGG GTGATGTCAGCTCATTGCAGTCTCTGCTTCCCGGGTTCAAGTGATCTTCCTGCCTCAGCCTCAGG T C KANSL1 Ensembl:ENSG00000120071 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1391828920 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13038744,Human_RBP_ID_17565974 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 39616 RMVar_ID_39616 Human_SNP_ID_625598128 A-to-I Human chr17 - 46171403 46171403 46171403 ATGGAACAGCCGGCACTTCAAGGAAGCAGTAGATTATCACCTGGTACAGACTCCAGCTCTAACTT ATGGAACAGCCGGCACTTCAAGGAAGCAGTAGTTTATCACCTGGTACAGACTCCAGCTCTAACTT T A KANSL1 Ensembl:ENSG00000120071 Protein coding CDS GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1881193 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1368624,Human_RBP_ID_1535368,Human_RBP_ID_1860325,Human_RBP_ID_5526338,Human_RBP_ID_5577404,Human_RBP_ID_6603144,Human_RBP_ID_9072763,Human_RBP_ID_13039087,Human_RBP_ID_17262935,Human_RBP_ID_18700026 Clinvar_Rec_116 GWAS_ID_4680,GWAS_ID_4681,GWAS_ID_4682,GWAS_ID_4683,GWAS_ID_4684,GWAS_ID_4685,GWAS_ID_4686,GWAS_ID_4687,GWAS_ID_4688,GWAS_ID_4689 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_308289,RMVar_hsa_circ_325152,RMVar_hsa_circ_365244,RMVar_hsa_circ_184850 39617 RMVar_ID_39617 Human_SNP_ID_625598129 A-to-I Human chr17 - 46171403 46171403 46171403 ATGGAACAGCCGGCACTTCAAGGAAGCAGTAGATTATCACCTGGTACAGACTCCAGCTCTAACTT ATGGAACAGCCGGCACTTCAAGGAAGCAGTAGGTTATCACCTGGTACAGACTCCAGCTCTAACTT T C KANSL1 Ensembl:ENSG00000120071 Protein coding CDS GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1881193 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_1368624,Human_RBP_ID_1535368,Human_RBP_ID_1860325,Human_RBP_ID_5526338,Human_RBP_ID_5577404,Human_RBP_ID_6603144,Human_RBP_ID_9072763,Human_RBP_ID_13039087,Human_RBP_ID_17262935,Human_RBP_ID_18700026 Clinvar_Rec_116 GWAS_ID_4680,GWAS_ID_4681,GWAS_ID_4682,GWAS_ID_4683,GWAS_ID_4684,GWAS_ID_4685,GWAS_ID_4686,GWAS_ID_4687,GWAS_ID_4688,GWAS_ID_4689 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_308289,RMVar_hsa_circ_325152,RMVar_hsa_circ_365244,RMVar_hsa_circ_184850 39618 RMVar_ID_39618 Human_SNP_ID_625598174 A-to-I Human chr17 - 46171471 46171471 46171471 GCCTTGATGTAGAACACACAACTTTGTATAGCAATAATAGCACTGCAAACAAATCCTCTGTCAAT GCCTTGATGTAGAACACACAACTTTGTATAGCGATAATAGCACTGCAAACAAATCCTCTGTCAAT T C KANSL1 Ensembl:ENSG00000120071 Protein coding CDS GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs35643216 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_300950,Human_RBP_ID_1535370,Human_RBP_ID_1860326,Human_RBP_ID_13039087,Human_RBP_ID_17262935,Human_RBP_ID_17491713,Human_RBP_ID_18700031,Human_RBP_ID_21890744,Human_RBP_ID_22805006,Human_RBP_ID_26963500,Human_RBP_ID_27453463 Human_miRNA_ID_2049912,Human_miRNA_ID_2049913,Human_miRNA_ID_2049914,Human_miRNA_ID_2049915,Human_miRNA_ID_2049916,Human_miRNA_ID_2049917 Clinvar_Rec_117 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_308289,RMVar_hsa_circ_325152,RMVar_hsa_circ_365244,RMVar_hsa_circ_184850 39619 RMVar_ID_39619 Human_SNP_ID_625602713 A-to-I Human chr17 - 46186261 46186261 46186261 CTCCTGCCTCAGCCTCCCGAGTAGCTGGAACTACAGGTGCCCGCCATCATGCTCAGCTAATTTTT CTCCTGCCTCAGCCTCCCGAGTAGCTGGAACTGCAGGTGCCCGCCATCATGCTCAGCTAATTTTT T C KANSL1 Ensembl:ENSG00000120071 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1004540296 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123012,RMVar_hsa_circ_184843,RMVar_hsa_circ_184839,RMVar_hsa_circ_117725,RMVar_hsa_circ_126756,RMVar_hsa_circ_94409,RMVar_hsa_circ_184846,RMVar_hsa_circ_109764,RMVar_hsa_circ_184847,RMVar_hsa_circ_184848 39620 RMVar_ID_39620 Human_SNP_ID_625656840 A-to-I Human chr17 + 46502366 46502366 46502366 GAGTTTCACTCTTGTTCCCCAGGCTAGAGTGCAATGGCCCGGTCTCTGCTCACTGCAATCTCTGC GAGTTTCACTCTTGTTCCCCAGGCTAGAGTGCGATGGCCCGGTCTCTGCTCACTGCAATCTCTGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1175410269 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85218,RMVar_hsa_circ_119037,RMVar_hsa_circ_184862,RMVar_hsa_circ_184863 39621 RMVar_ID_39621 Human_SNP_ID_625739660 A-to-I Human chr17 + 46941713 46941713 46941713 CTCATACCTCAGCCTCCTGAGTAGCTGGAACTACAAGTGTGTGCCACCATGTCTGGCTAATTTTT CTCATACCTCAGCCTCCTGAGTAGCTGGAACTGCAAGTGTGTGCCACCATGTCTGGCTAATTTTT A G AC005670.2,GOSR2 Ensembl:ENSG00000262633,Ensembl:ENSG00000108433 Protein coding,Protein coding intron,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1444441763 Functional Loss SNV dbSNP153 33..33 33 - - - 39622 RMVar_ID_39622 Human_SNP_ID_625741138 A-to-I Human chr17 + 46946748 46946748 46946748 AGCCAGGCAAGTTGGTGTGCGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGACATGAGAATTGTT AGCCAGGCAAGTTGGTGTGCGCCTGTAGTCCCGGCTACTTGGGAGGCTGAGACATGAGAATTGTT A G AC005670.2,GOSR2 Ensembl:ENSG00000262633,Ensembl:ENSG00000108433 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904559140 Functional Loss SNV dbSNP153 33..33 33 - - - 39623 RMVar_ID_39623 Human_SNP_ID_625743606 A-to-I Human chr17 + 46956516 46956516 46956516 CAGGGTTTCTGTCTCTACTGGTTGGCCAGGCTAGTCTCAAACTCCTGACCTCAGGTGATCCACCC CAGGGTTTCTGTCTCTACTGGTTGGCCAGGCTGGTCTCAAACTCCTGACCTCAGGTGATCCACCC A G AC005670.2,GOSR2 Ensembl:ENSG00000262633,Ensembl:ENSG00000108433 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935014445 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13219882 39624 RMVar_ID_39624 Human_SNP_ID_625756366 A-to-I Human chr17 - 47009081 47009081 47009081 TTGCCCCAGTTGGAGTGCAGTGATGTGATCTCAGTTCACTGCAGCCTCTGCCTCCCAGGTTCAAG TTGCCCCAGTTGGAGTGCAGTGATGTGATCTCGGTTCACTGCAGCCTCTGCCTCCCAGGTTCAAG T C AC005670.3 Ensembl:ENSG00000262879 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1441467032 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123012,RMVar_hsa_circ_184839,RMVar_hsa_circ_126756,RMVar_hsa_circ_184846 39625 RMVar_ID_39625 Human_SNP_ID_625772178 A-to-I Human chr17 - 47078225 47078225 47078225 CCCCATCTCTACTAAAAATACAAAAAAAAATTAGCCAGGTGTGGTGGCGAGTGCCTATAACCCCA CCCCATCTCTACTAAAAATACAAAAAAAAATTGGCCAGGTGTGGTGGCGAGTGCCTATAACCCCA T C AC005670.3 Ensembl:ENSG00000262879 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1166359318 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123012,RMVar_hsa_circ_184839,RMVar_hsa_circ_126756,RMVar_hsa_circ_184846 39626 RMVar_ID_39626 Human_SNP_ID_625775787 A-to-I Human chr17 - 47096068 47096068 47096068 CTCCCACCTCAGCCTCCCAAGTAGCTAGGACTAAAAGTATGTGCCACCATGCCCAGCTACTTTTA CTCCCACCTCAGCCTCCCAAGTAGCTAGGACTGAAAGTATGTGCCACCATGCCCAGCTACTTTTA T C AC005670.3 Ensembl:ENSG00000262879 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs969760116 Functional Loss SNV dbSNP153 33..33 33 - - - 39627 RMVar_ID_39627 Human_SNP_ID_625775857 A-to-I Human chr17 - 47096433 47096433 47096433 ATGGTGGCACACGCCTATAGTCCTCATTACTCAGGGGGCTGAGGCAAGAGGATCACTTGATTGAG ATGGTGGCACACGCCTATAGTCCTCATTACTCCGGGGGCTGAGGCAAGAGGATCACTTGATTGAG T G AC005670.3 Ensembl:ENSG00000262879 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs916302420 Functional Loss SNV dbSNP153 33..33 33 - - - 39628 RMVar_ID_39628 Human_SNP_ID_625784560 A-to-I Human chr17 - 47131783 47131783 47131783 ACACCTGTGGTCCTGGCTACTTGGGAGGCTGAAGCACAAGGATCACTTGAGCCCAGGAGTGCAAG ACACCTGTGGTCCTGGCTACTTGGGAGGCTGAGGCACAAGGATCACTTGAGCCCAGGAGTGCAAG T C CDC27 Ensembl:ENSG00000004897 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs78063747 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13044675 RMVar_hsa_circ_6284,RMVar_hsa_circ_23880,RMVar_hsa_circ_71891,RMVar_hsa_circ_126162,RMVar_hsa_circ_184890,RMVar_hsa_circ_63832,RMVar_hsa_circ_299857,RMVar_hsa_circ_24062,RMVar_hsa_circ_75496,RMVar_hsa_circ_44897,RMVar_hsa_circ_303808,RMVar_hsa_circ_358557,RMVar_hsa_circ_302762,RMVar_hsa_circ_61372,RMVar_hsa_circ_285557,RMVar_hsa_circ_47960,RMVar_hsa_circ_184892,RMVar_hsa_circ_184893,RMVar_hsa_circ_184894,RMVar_hsa_circ_184891 39629 RMVar_ID_39629 Human_SNP_ID_625784578 A-to-I Human chr17 - 47131813 47131813 47131813 AATTTAAAAATTAGCCTGGCATGGTGGTGCACACCTGTGGTCCTGGCTACTTGGGAGGCTGAAGC AATTTAAAAATTAGCCTGGCATGGTGGTGCACGCCTGTGGTCCTGGCTACTTGGGAGGCTGAAGC T C CDC27 Ensembl:ENSG00000004897 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs79810536 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13044675 RMVar_hsa_circ_6284,RMVar_hsa_circ_23880,RMVar_hsa_circ_71891,RMVar_hsa_circ_126162,RMVar_hsa_circ_184890,RMVar_hsa_circ_63832,RMVar_hsa_circ_299857,RMVar_hsa_circ_24062,RMVar_hsa_circ_75496,RMVar_hsa_circ_44897,RMVar_hsa_circ_303808,RMVar_hsa_circ_358557,RMVar_hsa_circ_302762,RMVar_hsa_circ_61372,RMVar_hsa_circ_285557,RMVar_hsa_circ_47960,RMVar_hsa_circ_184892,RMVar_hsa_circ_184893,RMVar_hsa_circ_184894,RMVar_hsa_circ_184891 39630 RMVar_ID_39630 Human_SNP_ID_625790995 A-to-I Human chr17 - 47155383 47155381 47155384 AAATTAGCCCGGCATGGTGACACATACGTGTAATCCCAGGTACTTTGGGGGTTGAGGCACAAGAA AAATTAGCCCGGCATGGTGACACATACGTGT___CCCAGGTACTTTGGGGGTTGAGGCACAAGAA GATT G CDC27 Ensembl:ENSG00000004897 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1244559189 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_6284,RMVar_hsa_circ_23880,RMVar_hsa_circ_126162,RMVar_hsa_circ_184890,RMVar_hsa_circ_358557,RMVar_hsa_circ_285557,RMVar_hsa_circ_74681,RMVar_hsa_circ_184891,RMVar_hsa_circ_61174,RMVar_hsa_circ_184900,RMVar_hsa_circ_275763,RMVar_hsa_circ_373077,RMVar_hsa_circ_20190,RMVar_hsa_circ_184901,RMVar_hsa_circ_334857,RMVar_hsa_circ_290408,RMVar_hsa_circ_184902,RMVar_hsa_circ_121510,RMVar_hsa_circ_306663,RMVar_hsa_circ_184903,RMVar_hsa_circ_353423,RMVar_hsa_circ_184906,RMVar_hsa_circ_336001,RMVar_hsa_circ_284768,RMVar_hsa_circ_339825,RMVar_hsa_circ_366588,RMVar_hsa_circ_377241,RMVar_hsa_circ_184907,RMVar_hsa_circ_306824 39631 RMVar_ID_39631 Human_SNP_ID_625790996 A-to-I Human chr17 - 47155383 47155383 47155383 AAATTAGCCCGGCATGGTGACACATACGTGTAATCCCAGGTACTTTGGGGGTTGAGGCACAAGAA AAATTAGCCCGGCATGGTGACACATACGTGTAGTCCCAGGTACTTTGGGGGTTGAGGCACAAGAA T C CDC27 Ensembl:ENSG00000004897 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs943752070 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6284,RMVar_hsa_circ_23880,RMVar_hsa_circ_126162,RMVar_hsa_circ_184890,RMVar_hsa_circ_358557,RMVar_hsa_circ_285557,RMVar_hsa_circ_74681,RMVar_hsa_circ_184891,RMVar_hsa_circ_61174,RMVar_hsa_circ_184900,RMVar_hsa_circ_275763,RMVar_hsa_circ_373077,RMVar_hsa_circ_20190,RMVar_hsa_circ_184901,RMVar_hsa_circ_334857,RMVar_hsa_circ_290408,RMVar_hsa_circ_184902,RMVar_hsa_circ_121510,RMVar_hsa_circ_306663,RMVar_hsa_circ_184903,RMVar_hsa_circ_353423,RMVar_hsa_circ_184906,RMVar_hsa_circ_336001,RMVar_hsa_circ_284768,RMVar_hsa_circ_339825,RMVar_hsa_circ_366588,RMVar_hsa_circ_377241,RMVar_hsa_circ_184907,RMVar_hsa_circ_306824 39632 RMVar_ID_39632 Human_SNP_ID_625791003 A-to-I Human chr17 - 47155390 47155390 47155390 ATTACAAAAATTAGCCCGGCATGGTGACACATACGTGTAATCCCAGGTACTTTGGGGGTTGAGGC ATTACAAAAATTAGCCCGGCATGGTGACACATGCGTGTAATCCCAGGTACTTTGGGGGTTGAGGC T C CDC27 Ensembl:ENSG00000004897 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1159802972 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6284,RMVar_hsa_circ_23880,RMVar_hsa_circ_126162,RMVar_hsa_circ_184890,RMVar_hsa_circ_358557,RMVar_hsa_circ_285557,RMVar_hsa_circ_74681,RMVar_hsa_circ_184891,RMVar_hsa_circ_61174,RMVar_hsa_circ_184900,RMVar_hsa_circ_275763,RMVar_hsa_circ_373077,RMVar_hsa_circ_20190,RMVar_hsa_circ_184901,RMVar_hsa_circ_334857,RMVar_hsa_circ_290408,RMVar_hsa_circ_184902,RMVar_hsa_circ_121510,RMVar_hsa_circ_306663,RMVar_hsa_circ_184903,RMVar_hsa_circ_353423,RMVar_hsa_circ_184906,RMVar_hsa_circ_336001,RMVar_hsa_circ_284768,RMVar_hsa_circ_339825,RMVar_hsa_circ_366588,RMVar_hsa_circ_377241,RMVar_hsa_circ_184907,RMVar_hsa_circ_306824 39633 RMVar_ID_39633 Human_SNP_ID_625791004 A-to-I Human chr17 - 47155392 47155392 47155392 AAATTACAAAAATTAGCCCGGCATGGTGACACATACGTGTAATCCCAGGTACTTTGGGGGTTGAG AAATTACAAAAATTAGCCCGGCATGGTGACACGTACGTGTAATCCCAGGTACTTTGGGGGTTGAG T C CDC27 Ensembl:ENSG00000004897 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs547990423 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6284,RMVar_hsa_circ_23880,RMVar_hsa_circ_126162,RMVar_hsa_circ_184890,RMVar_hsa_circ_358557,RMVar_hsa_circ_285557,RMVar_hsa_circ_74681,RMVar_hsa_circ_184891,RMVar_hsa_circ_61174,RMVar_hsa_circ_184900,RMVar_hsa_circ_275763,RMVar_hsa_circ_373077,RMVar_hsa_circ_20190,RMVar_hsa_circ_184901,RMVar_hsa_circ_334857,RMVar_hsa_circ_290408,RMVar_hsa_circ_184902,RMVar_hsa_circ_121510,RMVar_hsa_circ_306663,RMVar_hsa_circ_184903,RMVar_hsa_circ_353423,RMVar_hsa_circ_184906,RMVar_hsa_circ_336001,RMVar_hsa_circ_284768,RMVar_hsa_circ_339825,RMVar_hsa_circ_366588,RMVar_hsa_circ_377241,RMVar_hsa_circ_184907,RMVar_hsa_circ_306824 39634 RMVar_ID_39634 Human_SNP_ID_625791106 A-to-I Human chr17 - 47155870 47155870 47155870 TAGCTCACTGCAGCCTCAAATTCTTGGGCTCAAGCGATCCTCCCACCTCAGACTCCTGAGTAGCT TAGCTCACTGCAGCCTCAAATTCTTGGGCTCAGGCGATCCTCCCACCTCAGACTCCTGAGTAGCT T C CDC27 Ensembl:ENSG00000004897 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1280754272 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6284,RMVar_hsa_circ_23880,RMVar_hsa_circ_126162,RMVar_hsa_circ_184890,RMVar_hsa_circ_358557,RMVar_hsa_circ_285557,RMVar_hsa_circ_74681,RMVar_hsa_circ_184891,RMVar_hsa_circ_61174,RMVar_hsa_circ_184900,RMVar_hsa_circ_275763,RMVar_hsa_circ_373077,RMVar_hsa_circ_20190,RMVar_hsa_circ_184901,RMVar_hsa_circ_334857,RMVar_hsa_circ_290408,RMVar_hsa_circ_184902,RMVar_hsa_circ_121510,RMVar_hsa_circ_306663,RMVar_hsa_circ_184903,RMVar_hsa_circ_353423,RMVar_hsa_circ_184906,RMVar_hsa_circ_336001,RMVar_hsa_circ_284768,RMVar_hsa_circ_339825,RMVar_hsa_circ_366588,RMVar_hsa_circ_377241,RMVar_hsa_circ_184907,RMVar_hsa_circ_306824 39635 RMVar_ID_39635 Human_SNP_ID_625791114 A-to-I Human chr17 - 47155939 47155935 47155939 CACCTACCTTTTTTTGTTTGAGACAGGATCTCACTCTGTCACCCAGGTTAGAGTGCAGTGGCACA CACCTACCTTTTTTTGTTTGAGACAGGATCTC____TGTCACCCAGGTTAGAGTGCAGTGGCACA AGAGT A CDC27 Ensembl:ENSG00000004897 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1172776046 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_6284,RMVar_hsa_circ_23880,RMVar_hsa_circ_126162,RMVar_hsa_circ_184890,RMVar_hsa_circ_358557,RMVar_hsa_circ_285557,RMVar_hsa_circ_74681,RMVar_hsa_circ_184891,RMVar_hsa_circ_61174,RMVar_hsa_circ_184900,RMVar_hsa_circ_275763,RMVar_hsa_circ_373077,RMVar_hsa_circ_20190,RMVar_hsa_circ_184901,RMVar_hsa_circ_334857,RMVar_hsa_circ_290408,RMVar_hsa_circ_184902,RMVar_hsa_circ_121510,RMVar_hsa_circ_306663,RMVar_hsa_circ_184903,RMVar_hsa_circ_353423,RMVar_hsa_circ_184906,RMVar_hsa_circ_336001,RMVar_hsa_circ_284768,RMVar_hsa_circ_339825,RMVar_hsa_circ_366588,RMVar_hsa_circ_377241,RMVar_hsa_circ_184907,RMVar_hsa_circ_306824 39636 RMVar_ID_39636 Human_SNP_ID_625791189 A-to-I Human chr17 - 47156241 47156241 47156241 CCAGCTACTCGGGAGGCTGAGGCAAGAGAATCACTTGAACCCGGGAGACAGAGGTTGCAGTGAGC CCAGCTACTCGGGAGGCTGAGGCAAGAGAATCGCTTGAACCCGGGAGACAGAGGTTGCAGTGAGC T C CDC27 Ensembl:ENSG00000004897 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1266163694 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25292861 RMVar_hsa_circ_6284,RMVar_hsa_circ_23880,RMVar_hsa_circ_126162,RMVar_hsa_circ_184890,RMVar_hsa_circ_358557,RMVar_hsa_circ_285557,RMVar_hsa_circ_74681,RMVar_hsa_circ_184891,RMVar_hsa_circ_61174,RMVar_hsa_circ_184900,RMVar_hsa_circ_275763,RMVar_hsa_circ_373077,RMVar_hsa_circ_20190,RMVar_hsa_circ_184901,RMVar_hsa_circ_334857,RMVar_hsa_circ_290408,RMVar_hsa_circ_184902,RMVar_hsa_circ_121510,RMVar_hsa_circ_306663,RMVar_hsa_circ_184903,RMVar_hsa_circ_353423,RMVar_hsa_circ_184906,RMVar_hsa_circ_336001,RMVar_hsa_circ_284768,RMVar_hsa_circ_339825,RMVar_hsa_circ_366588,RMVar_hsa_circ_377241,RMVar_hsa_circ_184907,RMVar_hsa_circ_306824 39637 RMVar_ID_39637 Human_SNP_ID_625791211 A-to-I Human chr17 - 47156303 47156303 47156303 AAACCCCGTCTCTACTAAAAATACAAAAAACTAGCCGGGTGTGGTGGCACGCGCCTGTAGATCCA AAACCCCGTCTCTACTAAAAATACAAAAAACTGGCCGGGTGTGGTGGCACGCGCCTGTAGATCCA T C CDC27 Ensembl:ENSG00000004897 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1160242689 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6284,RMVar_hsa_circ_23880,RMVar_hsa_circ_126162,RMVar_hsa_circ_184890,RMVar_hsa_circ_358557,RMVar_hsa_circ_285557,RMVar_hsa_circ_74681,RMVar_hsa_circ_184891,RMVar_hsa_circ_61174,RMVar_hsa_circ_184900,RMVar_hsa_circ_275763,RMVar_hsa_circ_373077,RMVar_hsa_circ_20190,RMVar_hsa_circ_184901,RMVar_hsa_circ_334857,RMVar_hsa_circ_290408,RMVar_hsa_circ_184902,RMVar_hsa_circ_121510,RMVar_hsa_circ_306663,RMVar_hsa_circ_184903,RMVar_hsa_circ_353423,RMVar_hsa_circ_184906,RMVar_hsa_circ_336001,RMVar_hsa_circ_284768,RMVar_hsa_circ_339825,RMVar_hsa_circ_366588,RMVar_hsa_circ_377241,RMVar_hsa_circ_184907,RMVar_hsa_circ_306824 39638 RMVar_ID_39638 Human_SNP_ID_625792686 A-to-I Human chr17 - 47161711 47161711 47161711 GAGTCTCGCTCTGTCACCCAGGCTGGAGTGCAATGGCATGATCTCGACTCACTGTAACCTCCACC GAGTCTCGCTCTGTCACCCAGGCTGGAGTGCATTGGCATGATCTCGACTCACTGTAACCTCCACC T A CDC27,AC002558.3 Ensembl:ENSG00000004897,Ensembl:ENSG00000262265 Protein coding,lincRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1019812775 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1546795,Human_RBP_ID_3549552 Human_Splice_Rec_1831791 RMVar_hsa_circ_6284,RMVar_hsa_circ_23880,RMVar_hsa_circ_126162,RMVar_hsa_circ_184890,RMVar_hsa_circ_285557,RMVar_hsa_circ_184891,RMVar_hsa_circ_61174,RMVar_hsa_circ_184900,RMVar_hsa_circ_275763,RMVar_hsa_circ_373077,RMVar_hsa_circ_184901,RMVar_hsa_circ_334857,RMVar_hsa_circ_43453,RMVar_hsa_circ_290408,RMVar_hsa_circ_184902,RMVar_hsa_circ_121510,RMVar_hsa_circ_306663,RMVar_hsa_circ_184903,RMVar_hsa_circ_353423,RMVar_hsa_circ_184906,RMVar_hsa_circ_336001,RMVar_hsa_circ_339825,RMVar_hsa_circ_366588,RMVar_hsa_circ_377241,RMVar_hsa_circ_357361,RMVar_hsa_circ_302093 39639 RMVar_ID_39639 Human_SNP_ID_625792687 A-to-I Human chr17 - 47161711 47161711 47161711 GAGTCTCGCTCTGTCACCCAGGCTGGAGTGCAATGGCATGATCTCGACTCACTGTAACCTCCACC GAGTCTCGCTCTGTCACCCAGGCTGGAGTGCAGTGGCATGATCTCGACTCACTGTAACCTCCACC T C CDC27,AC002558.3 Ensembl:ENSG00000004897,Ensembl:ENSG00000262265 Protein coding,lincRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1019812775 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1546795,Human_RBP_ID_3549552 Human_Splice_Rec_1831791 RMVar_hsa_circ_6284,RMVar_hsa_circ_23880,RMVar_hsa_circ_126162,RMVar_hsa_circ_184890,RMVar_hsa_circ_285557,RMVar_hsa_circ_184891,RMVar_hsa_circ_61174,RMVar_hsa_circ_184900,RMVar_hsa_circ_275763,RMVar_hsa_circ_373077,RMVar_hsa_circ_184901,RMVar_hsa_circ_334857,RMVar_hsa_circ_43453,RMVar_hsa_circ_290408,RMVar_hsa_circ_184902,RMVar_hsa_circ_121510,RMVar_hsa_circ_306663,RMVar_hsa_circ_184903,RMVar_hsa_circ_353423,RMVar_hsa_circ_184906,RMVar_hsa_circ_336001,RMVar_hsa_circ_339825,RMVar_hsa_circ_366588,RMVar_hsa_circ_377241,RMVar_hsa_circ_357361,RMVar_hsa_circ_302093 39640 RMVar_ID_39640 Human_SNP_ID_625793158 A-to-I Human chr17 - 47164039 47164039 47164039 CTTATGGGGGCCAGGCAGGGTGGCTCACACCTATAATCCCAGCATTTTGGGAGGCCGAGGCGGGC CTTATGGGGGCCAGGCAGGGTGGCTCACACCTGTAATCCCAGCATTTTGGGAGGCCGAGGCGGGC T C CDC27,AC002558.3 Ensembl:ENSG00000004897,Ensembl:ENSG00000262265 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs550462707 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6284,RMVar_hsa_circ_23880,RMVar_hsa_circ_126162,RMVar_hsa_circ_184890,RMVar_hsa_circ_285557,RMVar_hsa_circ_184891,RMVar_hsa_circ_61174,RMVar_hsa_circ_184900,RMVar_hsa_circ_275763,RMVar_hsa_circ_373077,RMVar_hsa_circ_184901,RMVar_hsa_circ_334857,RMVar_hsa_circ_43453,RMVar_hsa_circ_290408,RMVar_hsa_circ_184902,RMVar_hsa_circ_121510,RMVar_hsa_circ_306663,RMVar_hsa_circ_184903,RMVar_hsa_circ_353423,RMVar_hsa_circ_184906,RMVar_hsa_circ_336001,RMVar_hsa_circ_339825,RMVar_hsa_circ_366588,RMVar_hsa_circ_377241,RMVar_hsa_circ_357361,RMVar_hsa_circ_302093 39641 RMVar_ID_39641 Human_SNP_ID_625827916 A-to-I Human chr17 + 47312497 47312497 47312497 TGTGGAAGCTCATGCCTGTAATTATAACCTTCAGCTACTAAGACAGGTGTGGTGGCTCACGCCTG TGTGGAAGCTCATGCCTGTAATTATAACCTTCGGCTACTAAGACAGGTGTGGTGGCTCACGCCTG A G ITGB3,AC068234.1 Ensembl:ENSG00000259207,Ensembl:ENSG00000259753 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs999831726 Functional Loss SNV dbSNP153 33..33 33 - - - 39642 RMVar_ID_39642 Human_SNP_ID_625855839 A-to-I Human chr17 - 47435592 47435592 47435592 TCAGTAGTTCTTCTATACACCAACAGTGACCAAGTGGAGAACCAAATCAAGAACTCAACCCCTTT TCAGTAGTTCTTCTATACACCAACAGTGACCAGGTGGAGAACCAAATCAAGAACTCAACCCCTTT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054804305 Functional Loss SNV dbSNP153 33..33 33 - - - 39643 RMVar_ID_39643 Human_SNP_ID_625855844 A-to-I Human chr17 - 47435610 47435610 47435610 AAGATTACTGTACACAAATCAGTAGTTCTTCTATACACCAACAGTGACCAAGTGGAGAACCAAAT AAGATTACTGTACACAAATCAGTAGTTCTTCTGTACACCAACAGTGACCAAGTGGAGAACCAAAT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1402130105 Functional Loss SNV dbSNP153 33..33 33 - - - 39644 RMVar_ID_39644 Human_SNP_ID_625855846 A-to-I Human chr17 - 47435619 47435619 47435619 TCCAGATACAAGATTACTGTACACAAATCAGTAGTTCTTCTATACACCAACAGTGACCAAGTGGA TCCAGATACAAGATTACTGTACACAAATCAGTGGTTCTTCTATACACCAACAGTGACCAAGTGGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs918081751 Functional Loss SNV dbSNP153 33..33 33 - - - 39645 RMVar_ID_39645 Human_SNP_ID_625855847 A-to-I Human chr17 - 47435625 47435624 47435625 AAAGCTTCCAGATACAAGATTACTGTACACAAATCAGTAGTTCTTCTATACACCAACAGTGACCA AAAGCTTCCAGATACAAGATTACTGTACACAA_TCAGTAGTTCTTCTATACACCAACAGTGACCA AT A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348954450 Functional Loss DEL dbSNP153 33..33 33 - - - 39646 RMVar_ID_39646 Human_SNP_ID_625856168 A-to-I Human chr17 + 47437121 47437121 47437121 TGATTTCCAGTTTTATTCCATTGTGGCCAGAGAGAGTGCTTGATATAATTTCAATTTTCTTAAAT TGATTTCCAGTTTTATTCCATTGTGGCCAGAGGGAGTGCTTGATATAATTTCAATTTTCTTAAAT A G EFCAB13 Ensembl:ENSG00000178852 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1322940613 Functional Loss SNV dbSNP153 33..33 33 - - - 39647 RMVar_ID_39647 Human_SNP_ID_625857612 A-to-I Human chr17 - 47443833 47443833 47443833 GCAAGGCTGAGGCAAGAGGTTGCTTGAGCCCAAGAGTTGGAGGCTGCAGTGAACCATGATCATGC GCAAGGCTGAGGCAAGAGGTTGCTTGAGCCCAGGAGTTGGAGGCTGCAGTGAACCATGATCATGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1372810802 Functional Loss SNV dbSNP153 33..33 33 - - - 39648 RMVar_ID_39648 Human_SNP_ID_625857853 A-to-I Human chr17 - 47445263 47445263 47445263 TGGTAGAGAGACAGCGTCTTGCTATATAGCCCAGGCTGGTCATGAACTCCTGGCCTCAAGTTATC TGGTAGAGAGACAGCGTCTTGCTATATAGCCCTGGCTGGTCATGAACTCCTGGCCTCAAGTTATC T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006693573 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9865041,Human_RBP_ID_13046673 39649 RMVar_ID_39649 Human_SNP_ID_625857854 A-to-I Human chr17 - 47445263 47445263 47445263 TGGTAGAGAGACAGCGTCTTGCTATATAGCCCAGGCTGGTCATGAACTCCTGGCCTCAAGTTATC TGGTAGAGAGACAGCGTCTTGCTATATAGCCCGGGCTGGTCATGAACTCCTGGCCTCAAGTTATC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006693573 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9865041,Human_RBP_ID_13046673 39650 RMVar_ID_39650 Human_SNP_ID_625857886 A-to-I Human chr17 - 47445343 47445343 47445343 CCACCTCAGCCTCTCAAGTAGCTAGGAGTACAAGTGCCACCACCACACCCAGTTTTTTTTTTTTT CCACCTCAGCCTCTCAAGTAGCTAGGAGTACAGGTGCCACCACCACACCCAGTTTTTTTTTTTTT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1193818701 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6605063 39651 RMVar_ID_39651 Human_SNP_ID_625857889 A-to-I Human chr17 - 47445352 47445352 47445352 TCCGTCCTCCCACCTCAGCCTCTCAAGTAGCTAGGAGTACAAGTGCCACCACCACACCCAGTTTT TCCGTCCTCCCACCTCAGCCTCTCAAGTAGCTGGGAGTACAAGTGCCACCACCACACCCAGTTTT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs952347367 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6605063 39652 RMVar_ID_39652 Human_SNP_ID_625858986 A-to-I Human chr17 - 47450301 47450301 47450301 TTGAGCCTGGGAGGTCAAGGCTGCAGTGAGCTATGATTGTGTGACTGTACTCCAGCCCAGGTAAC TTGAGCCTGGGAGGTCAAGGCTGCAGTGAGCTCTGATTGTGTGACTGTACTCCAGCCCAGGTAAC T G lnc-CDC27-9 RNACentral:URS00008C3D4A lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs535317242 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1535662 39653 RMVar_ID_39653 Human_SNP_ID_625859058 A-to-I Human chr17 - 47450702 47450702 47450702 GGTGTGGGGAGGCACATGTGTCTGTAGTCCCAACTACTCAAGAGGCTGCGGTGGGAGGGTCCCTT GGTGTGGGGAGGCACATGTGTCTGTAGTCCCAGCTACTCAAGAGGCTGCGGTGGGAGGGTCCCTT T C MRPL45P2 Ensembl:ENSG00000228782 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1403166615 Functional Loss SNV dbSNP153 33..33 33 - - - 39654 RMVar_ID_39654 Human_SNP_ID_625859224 A-to-I Human chr17 - 47451666 47451666 47451666 GTTTTCTGTATTATTTGTAGAGTTGAGATTTCATCATGTTGCCCAGGCTGGTCTTGAACTCCTGA GTTTTCTGTATTATTTGTAGAGTTGAGATTTCCTCATGTTGCCCAGGCTGGTCTTGAACTCCTGA T G MRPL45P2 Ensembl:ENSG00000228782 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1003221895 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13046778 39655 RMVar_ID_39655 Human_SNP_ID_625859247 A-to-I Human chr17 - 47451788 47451788 47451788 GCTGGAGTGCAGTGGTGCAGTTTTGGCTCACTACAGCCTTGACCTCTTGGGCTCAAGCAGTCCTT GCTGGAGTGCAGTGGTGCAGTTTTGGCTCACTGCAGCCTTGACCTCTTGGGCTCAAGCAGTCCTT T C MRPL45P2 Ensembl:ENSG00000228782 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs557228335 Functional Loss SNV dbSNP153 33..33 33 - - - 39656 RMVar_ID_39656 Human_SNP_ID_625859379 A-to-I Human chr17 - 47452501 47452501 47452501 TGGTGGACGCCTGTAATCCCAGCTATTCGGGAAGCTGAGACAGGAGAATTGCTTGAACCTGGGAG TGGTGGACGCCTGTAATCCCAGCTATTCGGGAGGCTGAGACAGGAGAATTGCTTGAACCTGGGAG T C MRPL45P2 Ensembl:ENSG00000228782 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1220770399 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17379230 39657 RMVar_ID_39657 Human_SNP_ID_625863052 A-to-I Human chr17 - 47470202 47470202 47470202 TCAGCTCACTGCAACATCCACTTCCTGGCTCAAGTGATCCTCCAGCCTCAGCCTCCCAAGTAGCT TCAGCTCACTGCAACATCCACTTCCTGGCTCAGGTGATCCTCCAGCCTCAGCCTCCCAAGTAGCT T C MRPL45P2 Ensembl:ENSG00000228782 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1375181608 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6605110,Human_RBP_ID_18514334,Human_RBP_ID_23731054 RMVar_hsa_circ_35829,RMVar_hsa_circ_325396,RMVar_hsa_circ_184936,RMVar_hsa_circ_24572 39658 RMVar_ID_39658 Human_SNP_ID_625863103 A-to-I Human chr17 - 47470590 47470590 47470590 GAACTCCTGGCCTCAAGTGATCCACCTGCCTCAGCCTACCAAAGTGCTGGGGTTACAGGCATGAG GAACTCCTGGCCTCAAGTGATCCACCTGCCTCTGCCTACCAAAGTGCTGGGGTTACAGGCATGAG T A MRPL45P2 Ensembl:ENSG00000228782 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs895083186 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17379240 RMVar_hsa_circ_35829,RMVar_hsa_circ_325396,RMVar_hsa_circ_184936,RMVar_hsa_circ_24572 39659 RMVar_ID_39659 Human_SNP_ID_625863128 A-to-I Human chr17 - 47470699 47470699 47470699 CTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCTTGCACCACCACGCCTGGGTAATTTTT CTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTGCAGGCTTGCACCACCACGCCTGGGTAATTTTT T C MRPL45P2 Ensembl:ENSG00000228782 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1374526417 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35829,RMVar_hsa_circ_325396,RMVar_hsa_circ_184936,RMVar_hsa_circ_24572 39660 RMVar_ID_39660 Human_SNP_ID_625863963 A-to-I Human chr17 - 47474364 47474364 47474364 TGGTTCACTGCAGCCTCCGCCTCCTGGGTTCAAGAGGTTCTTGTACTTCAGCCTCCCAAGTAGCT TGGTTCACTGCAGCCTCCGCCTCCTGGGTTCAGGAGGTTCTTGTACTTCAGCCTCCCAAGTAGCT T C MRPL45P2 Ensembl:ENSG00000228782 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459561047 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35829,RMVar_hsa_circ_325396,RMVar_hsa_circ_184936,RMVar_hsa_circ_24572 39661 RMVar_ID_39661 Human_SNP_ID_625864772 A-to-I Human chr17 - 47477000 47477000 47477000 TTTGAGGGGCTGGGTGGTGGCTCATACCCATAATCCAGCACTTTTGGAGGCCGAAGTGGGAGGAT TTTGAGGGGCTGGGTGGTGGCTCATACCCATAGTCCAGCACTTTTGGAGGCCGAAGTGGGAGGAT T C MRPL45P2 Ensembl:ENSG00000228782 Pseudogene intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs981622114 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_819491,Human_RBP_ID_8727764,Human_RBP_ID_13232943,Human_RBP_ID_17565983,Human_RBP_ID_24372807 RMVar_hsa_circ_35829,RMVar_hsa_circ_325396,RMVar_hsa_circ_184936,RMVar_hsa_circ_24572 39662 RMVar_ID_39662 Human_SNP_ID_625867670 A-to-I Human chr17 - 47488827 47488827 47488827 CCTGACCAACGTGGAGAAACCTCGTCTCTACTAAAAATGCAAAATTAGCCGGGCGTGGTGGCACA CCTGACCAACGTGGAGAAACCTCGTCTCTACTGAAAATGCAAAATTAGCCGGGCGTGGTGGCACA T C MRPL45P2 Ensembl:ENSG00000228782 Pseudogene intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,31158229,32596459 RNA-Seq:(High) rs1357177108 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17380033 RMVar_hsa_circ_35829,RMVar_hsa_circ_325396,RMVar_hsa_circ_184936,RMVar_hsa_circ_296625 39663 RMVar_ID_39663 Human_SNP_ID_625878854 A-to-I Human chr17 + 47534276 47534276 47534276 ACTGCACCCAGCTAATTTTTTGTATTTTTAGTAGAGACAGGGTTTTACTGTGGTCTCGACCTCCT ACTGCACCCAGCTAATTTTTTGTATTTTTAGTGGAGACAGGGTTTTACTGTGGTCTCGACCTCCT A G NPEPPS Ensembl:ENSG00000141279 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs564801328 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_184938,RMVar_hsa_circ_83472,RMVar_hsa_circ_113966,RMVar_hsa_circ_184940 39664 RMVar_ID_39664 Human_SNP_ID_625879643 A-to-I Human chr17 + 47536487 47536487 47536487 TGATCTCGGCTCACCGCAGCCTCTGCCCCCCCAGGTTCAAGCAATTCTCCTGCCTTAGCCTCCCA TGATCTCGGCTCACCGCAGCCTCTGCCCCCCCGGGTTCAAGCAATTCTCCTGCCTTAGCCTCCCA A G NPEPPS Ensembl:ENSG00000141279 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs543541837 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_184938,RMVar_hsa_circ_83472,RMVar_hsa_circ_113966,RMVar_hsa_circ_184940 39665 RMVar_ID_39665 Human_SNP_ID_625895351 A-to-I Human chr17 + 47600079 47600079 47600079 TGACCTCGAGATCCGCCTGCCTCAGCCTCCCAAAGTGTTGGTATTACAGGTGTGAGTCACTGTGC TGACCTCGAGATCCGCCTGCCTCAGCCTCCCAGAGTGTTGGTATTACAGGTGTGAGTCACTGTGC A G NPEPPS Ensembl:ENSG00000141279 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs920554658 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17565985 RMVar_hsa_circ_73355,RMVar_hsa_circ_57789,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_184970 39666 RMVar_ID_39666 Human_SNP_ID_625897210 A-to-I Human chr17 + 47607868 47607867 47607869 GCTGTAGAAACATTTTTTTCTTTTAAAGATACAGAGTCTCGCTCTGTTGCCGAGGCTGGAGTGCA GCTGTAGAAACATTTTTTTCTTTTAAAGATAC__AGTCTCGCTCTGTTGCCGAGGCTGGAGTGCA CAG C NPEPPS Ensembl:ENSG00000141279 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1247456133 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_73355,RMVar_hsa_circ_57789,RMVar_hsa_circ_18674,RMVar_hsa_circ_281434,RMVar_hsa_circ_351877,RMVar_hsa_circ_343398,RMVar_hsa_circ_300423,RMVar_hsa_circ_184963,RMVar_hsa_circ_19790,RMVar_hsa_circ_184962,RMVar_hsa_circ_43407,RMVar_hsa_circ_298544,RMVar_hsa_circ_300211,RMVar_hsa_circ_98854,RMVar_hsa_circ_184964,RMVar_hsa_circ_184965,RMVar_hsa_circ_45870,RMVar_hsa_circ_342818,RMVar_hsa_circ_184972,RMVar_hsa_circ_284235,RMVar_hsa_circ_184975,RMVar_hsa_circ_184976,RMVar_hsa_circ_184974,RMVar_hsa_circ_184977,RMVar_hsa_circ_318496 39667 RMVar_ID_39667 Human_SNP_ID_625897277 A-to-I Human chr17 + 47608186 47608186 47608186 TGGGTGTAAAAGGGAATCAGGCCAGGCGTGGTAGCTCACACCCGTAATCCCAGCACTTTGGAAGG TGGGTGTAAAAGGGAATCAGGCCAGGCGTGGTGGCTCACACCCGTAATCCCAGCACTTTGGAAGG A G NPEPPS Ensembl:ENSG00000141279 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1305650606 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17565988 RMVar_hsa_circ_73355,RMVar_hsa_circ_57789,RMVar_hsa_circ_18674,RMVar_hsa_circ_281434,RMVar_hsa_circ_351877,RMVar_hsa_circ_343398,RMVar_hsa_circ_300423,RMVar_hsa_circ_184963,RMVar_hsa_circ_19790,RMVar_hsa_circ_184962,RMVar_hsa_circ_43407,RMVar_hsa_circ_298544,RMVar_hsa_circ_300211,RMVar_hsa_circ_98854,RMVar_hsa_circ_184964,RMVar_hsa_circ_184965,RMVar_hsa_circ_45870,RMVar_hsa_circ_342818,RMVar_hsa_circ_184972,RMVar_hsa_circ_284235,RMVar_hsa_circ_184975,RMVar_hsa_circ_184976,RMVar_hsa_circ_184974,RMVar_hsa_circ_184977,RMVar_hsa_circ_318496 39668 RMVar_ID_39668 Human_SNP_ID_625904703 A-to-I Human chr17 - 47638437 47638429 47638437 TAATGATGTTGAACATTTTTTTTTTTTTTTTTAGATGGAGTCTCACTCTGTCACCCAGGCTGGAG TAATGATGTTGAACATTTTTTTTTTTTTTTTT________TCTCACTCTGTCACCCAGGCTGGAG ACTCCATCT A AC025682.2 Ensembl:ENSG00000263766 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1455774978 Functional Loss DEL dbSNP153 33..40 33 - - - 39669 RMVar_ID_39669 Human_SNP_ID_625904707 A-to-I Human chr17 - 47638437 47638437 47638437 TAATGATGTTGAACATTTTTTTTTTTTTTTTTAGATGGAGTCTCACTCTGTCACCCAGGCTGGAG TAATGATGTTGAACATTTTTTTTTTTTTTTTTTGATGGAGTCTCACTCTGTCACCCAGGCTGGAG T A AC025682.2 Ensembl:ENSG00000263766 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1442649277 Functional Loss SNV dbSNP153 33..33 33 - - - 39670 RMVar_ID_39670 Human_SNP_ID_625905527 A-to-I Human chr17 - 47642152 47642152 47642152 GGGGGTATTTTTTGTAGAAATGGGGTTTTGTCATGTTGCCCGGGCTGGTCTCAAACTCCTGGGCT GGGGGTATTTTTTGTAGAAATGGGGTTTTGTCCTGTTGCCCGGGCTGGTCTCAAACTCCTGGGCT T G AC025682.2 Ensembl:ENSG00000263766 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1368088786 Functional Loss SNV dbSNP153 33..33 33 - - - 39671 RMVar_ID_39671 Human_SNP_ID_625913769 A-to-I Human chr17 + 47672186 47672186 47672186 CACCAACATGCCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCGCCATGTTGGCCAGGC CACCAACATGCCTGGCTAATTTTTGTATTTTTGGTAGAGATGGGGTTTCGCCATGTTGGCCAGGC A G KPNB1 Ensembl:ENSG00000108424 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs185505943 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_373290,RMVar_hsa_circ_375901,RMVar_hsa_circ_353897,RMVar_hsa_circ_62822,RMVar_hsa_circ_184994,RMVar_hsa_circ_42980,RMVar_hsa_circ_184993,RMVar_hsa_circ_376640,RMVar_hsa_circ_24523,RMVar_hsa_circ_3055,RMVar_hsa_circ_111711,RMVar_hsa_circ_92241,RMVar_hsa_circ_184995,RMVar_hsa_circ_296207,RMVar_hsa_circ_185003,RMVar_hsa_circ_271528,RMVar_hsa_circ_344601,RMVar_hsa_circ_369047,RMVar_hsa_circ_99626,RMVar_hsa_circ_96010,RMVar_hsa_circ_185005,RMVar_hsa_circ_185007,RMVar_hsa_circ_185006,RMVar_hsa_circ_281671,RMVar_hsa_circ_319953,RMVar_hsa_circ_185004,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_185019,RMVar_hsa_circ_185016,RMVar_hsa_circ_185017,RMVar_hsa_circ_185015,RMVar_hsa_circ_185012,RMVar_hsa_circ_185013,RMVar_hsa_circ_370082,RMVar_hsa_circ_185026,RMVar_hsa_circ_185027,RMVar_hsa_circ_312552,RMVar_hsa_circ_347877,RMVar_hsa_circ_185030,RMVar_hsa_circ_75902,RMVar_hsa_circ_348613,RMVar_hsa_circ_185033,RMVar_hsa_circ_185034 39672 RMVar_ID_39672 Human_SNP_ID_625913794 A-to-I Human chr17 + 47672255 47672255 47672255 CACAAACTCCTGACACCTCAGGTGATCTGCCCACCTTGGCCTCCCAAAGTGCTGGGATTGTAGGC CACAAACTCCTGACACCTCAGGTGATCTGCCCGCCTTGGCCTCCCAAAGTGCTGGGATTGTAGGC A G KPNB1 Ensembl:ENSG00000108424 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031543281 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25294371 RMVar_hsa_circ_373290,RMVar_hsa_circ_375901,RMVar_hsa_circ_353897,RMVar_hsa_circ_62822,RMVar_hsa_circ_184994,RMVar_hsa_circ_42980,RMVar_hsa_circ_184993,RMVar_hsa_circ_376640,RMVar_hsa_circ_24523,RMVar_hsa_circ_3055,RMVar_hsa_circ_111711,RMVar_hsa_circ_92241,RMVar_hsa_circ_184995,RMVar_hsa_circ_296207,RMVar_hsa_circ_185003,RMVar_hsa_circ_271528,RMVar_hsa_circ_344601,RMVar_hsa_circ_369047,RMVar_hsa_circ_99626,RMVar_hsa_circ_96010,RMVar_hsa_circ_185005,RMVar_hsa_circ_185007,RMVar_hsa_circ_185006,RMVar_hsa_circ_281671,RMVar_hsa_circ_319953,RMVar_hsa_circ_185004,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_185019,RMVar_hsa_circ_185016,RMVar_hsa_circ_185017,RMVar_hsa_circ_185015,RMVar_hsa_circ_185012,RMVar_hsa_circ_185013,RMVar_hsa_circ_370082,RMVar_hsa_circ_185026,RMVar_hsa_circ_185027,RMVar_hsa_circ_312552,RMVar_hsa_circ_347877,RMVar_hsa_circ_185030,RMVar_hsa_circ_75902,RMVar_hsa_circ_348613,RMVar_hsa_circ_185033,RMVar_hsa_circ_185034 39673 RMVar_ID_39673 Human_SNP_ID_625913879 A-to-I Human chr17 + 47672571 47672571 47672571 AGCCACTACACCTGGCTAATTTTTATATTTTTAGTAGAGGTGGGGTTTCACCATGTTGACCAGGC AGCCACTACACCTGGCTAATTTTTATATTTTTGGTAGAGGTGGGGTTTCACCATGTTGACCAGGC A G KPNB1 Ensembl:ENSG00000108424 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1330067985 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_373290,RMVar_hsa_circ_375901,RMVar_hsa_circ_353897,RMVar_hsa_circ_62822,RMVar_hsa_circ_184994,RMVar_hsa_circ_42980,RMVar_hsa_circ_184993,RMVar_hsa_circ_376640,RMVar_hsa_circ_24523,RMVar_hsa_circ_3055,RMVar_hsa_circ_111711,RMVar_hsa_circ_92241,RMVar_hsa_circ_184995,RMVar_hsa_circ_296207,RMVar_hsa_circ_185003,RMVar_hsa_circ_271528,RMVar_hsa_circ_344601,RMVar_hsa_circ_369047,RMVar_hsa_circ_99626,RMVar_hsa_circ_96010,RMVar_hsa_circ_185005,RMVar_hsa_circ_185007,RMVar_hsa_circ_185006,RMVar_hsa_circ_281671,RMVar_hsa_circ_319953,RMVar_hsa_circ_185004,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_185019,RMVar_hsa_circ_185016,RMVar_hsa_circ_185017,RMVar_hsa_circ_185015,RMVar_hsa_circ_185012,RMVar_hsa_circ_185013,RMVar_hsa_circ_370082,RMVar_hsa_circ_185026,RMVar_hsa_circ_185027,RMVar_hsa_circ_312552,RMVar_hsa_circ_347877,RMVar_hsa_circ_185030,RMVar_hsa_circ_75902,RMVar_hsa_circ_348613,RMVar_hsa_circ_185033,RMVar_hsa_circ_185034 39674 RMVar_ID_39674 Human_SNP_ID_625914233 A-to-I Human chr17 + 47674201 47674201 47674201 TTTGATGGGAGAAGTCAGGTTGGTTTGATTTTATCAAGTTTATTTCTAGGTCATCTGTAAATAGG TTTGATGGGAGAAGTCAGGTTGGTTTGATTTTGTCAAGTTTATTTCTAGGTCATCTGTAAATAGG A G KPNB1 Ensembl:ENSG00000108424 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs937465374 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17565990,Human_RBP_ID_17894401 RMVar_hsa_circ_373290,RMVar_hsa_circ_375901,RMVar_hsa_circ_62822,RMVar_hsa_circ_184994,RMVar_hsa_circ_184993,RMVar_hsa_circ_376640,RMVar_hsa_circ_24523,RMVar_hsa_circ_3055,RMVar_hsa_circ_184995,RMVar_hsa_circ_296207,RMVar_hsa_circ_185003,RMVar_hsa_circ_271528,RMVar_hsa_circ_344601,RMVar_hsa_circ_369047,RMVar_hsa_circ_99626,RMVar_hsa_circ_96010,RMVar_hsa_circ_185005,RMVar_hsa_circ_185006,RMVar_hsa_circ_281671,RMVar_hsa_circ_319953,RMVar_hsa_circ_185004,RMVar_hsa_circ_273878,RMVar_hsa_circ_126447,RMVar_hsa_circ_125485,RMVar_hsa_circ_185014,RMVar_hsa_circ_78934,RMVar_hsa_circ_89112,RMVar_hsa_circ_185018,RMVar_hsa_circ_185016,RMVar_hsa_circ_185017,RMVar_hsa_circ_185015,RMVar_hsa_circ_185012,RMVar_hsa_circ_185013,RMVar_hsa_circ_370082,RMVar_hsa_circ_185026,RMVar_hsa_circ_185027,RMVar_hsa_circ_312552,RMVar_hsa_circ_347877,RMVar_hsa_circ_185030,RMVar_hsa_circ_101612,RMVar_hsa_circ_75902,RMVar_hsa_circ_185034,RMVar_hsa_circ_337604,RMVar_hsa_circ_185035,RMVar_hsa_circ_269724,RMVar_hsa_circ_348763 39675 RMVar_ID_39675 Human_SNP_ID_625914758 A-to-I Human chr17 + 47675947 47675947 47675947 AAAGAAGTTAATTTTGGCTCCTGGAGTGGCTGATTTGGATCTGAAGCCCAGTGCTGCTTTTCCTG AAAGAAGTTAATTTTGGCTCCTGGAGTGGCTGGTTTGGATCTGAAGCCCAGTGCTGCTTTTCCTG A G KPNB1 Ensembl:ENSG00000108424 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1419262255 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_821180,Human_RBP_ID_6605706,Human_RBP_ID_13049277 RMVar_hsa_circ_373290,RMVar_hsa_circ_62822,RMVar_hsa_circ_184994,RMVar_hsa_circ_24523,RMVar_hsa_circ_3055,RMVar_hsa_circ_8154,RMVar_hsa_circ_344601,RMVar_hsa_circ_369047,RMVar_hsa_circ_99626,RMVar_hsa_circ_96010,RMVar_hsa_circ_185005,RMVar_hsa_circ_319953,RMVar_hsa_circ_185004,RMVar_hsa_circ_273878,RMVar_hsa_circ_126447,RMVar_hsa_circ_125485,RMVar_hsa_circ_185014,RMVar_hsa_circ_78934,RMVar_hsa_circ_89112,RMVar_hsa_circ_185016,RMVar_hsa_circ_185017,RMVar_hsa_circ_185015,RMVar_hsa_circ_185012,RMVar_hsa_circ_185013,RMVar_hsa_circ_185026,RMVar_hsa_circ_347877,RMVar_hsa_circ_337604,RMVar_hsa_circ_269724,RMVar_hsa_circ_348763 39676 RMVar_ID_39676 Human_SNP_ID_625954769 A-to-I Human chr17 - 47829767 47829767 47829767 CTCATGGCTCAGCCACCTGAGTAGCTGGGACTACAGGTGTGTGCCACCACGCCTGGCTAATTTTT CTCATGGCTCAGCCACCTGAGTAGCTGGGACTCCAGGTGTGTGCCACCACGCCTGGCTAATTTTT T G MRPL10 Ensembl:ENSG00000159111 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs577300145 Functional Loss SNV dbSNP153 33..33 33 - - - 39677 RMVar_ID_39677 Human_SNP_ID_625954783 A-to-I Human chr17 - 47829843 47829843 47829843 ACCCAGGCCGGAGTGCCGGAGTGCAATGGCACAATCTCGGCTCACTGCAACCTCTGCCTCTTGGG ACCCAGGCCGGAGTGCCGGAGTGCAATGGCACGATCTCGGCTCACTGCAACCTCTGCCTCTTGGG T C MRPL10 Ensembl:ENSG00000159111 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1034300621 Functional Loss SNV dbSNP153 33..33 33 - - - 39678 RMVar_ID_39678 Human_SNP_ID_625970019 A-to-I Human chr17 - 47889453 47889453 47889453 GACCCCCATCTCTACAAAAAAATTTAAAAATTAGCCAGGCTTGGTGGCTCTCAACTGTAGTCCCA GACCCCCATCTCTACAAAAAAATTTAAAAATTGGCCAGGCTTGGTGGCTCTCAACTGTAGTCCCA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs975699604 Functional Loss SNV dbSNP153 33..33 33 - - - 39679 RMVar_ID_39679 Human_SNP_ID_625976349 A-to-I Human chr17 + 47916469 47916469 47916469 AGGGACCCGATCAAATGCCAATATCCAGTACCAGGCGGTCCCTCAGATTCAGGCAAGCAATTCCC AGGGACCCGATCAAATGCCAATATCCAGTACCCGGCGGTCCCTCAGATTCAGGCAAGCAATTCCC A C SP2 Ensembl:ENSG00000167182 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs746404445 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13050691,Human_RBP_ID_17262966,Human_RBP_ID_26813756 Human_miRNA_ID_891548,Human_miRNA_ID_2352142,Human_miRNA_ID_2404446,Human_miRNA_ID_3047688 RMVar_hsa_circ_36992,RMVar_hsa_circ_315170,RMVar_hsa_circ_185053 39680 RMVar_ID_39680 Human_SNP_ID_625976350 A-to-I Human chr17 + 47916469 47916469 47916469 AGGGACCCGATCAAATGCCAATATCCAGTACCAGGCGGTCCCTCAGATTCAGGCAAGCAATTCCC AGGGACCCGATCAAATGCCAATATCCAGTACCGGGCGGTCCCTCAGATTCAGGCAAGCAATTCCC A G SP2 Ensembl:ENSG00000167182 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs746404445 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13050691,Human_RBP_ID_17262966,Human_RBP_ID_26813756 Human_miRNA_ID_891548,Human_miRNA_ID_2352142,Human_miRNA_ID_2404446,Human_miRNA_ID_3047688 RMVar_hsa_circ_36992,RMVar_hsa_circ_315170,RMVar_hsa_circ_185053 39681 RMVar_ID_39681 Human_SNP_ID_626027424 A-to-I Human chr17 + 48115251 48115251 48115251 GCCCAGCTAATTTTTGTGTTTTTAGTAGTGACAGGGTTTTACCATGCTAGCCAGGCTGGTCTCGA GCCCAGCTAATTTTTGTGTTTTTAGTAGTGACGGGGTTTTACCATGCTAGCCAGGCTGGTCTCGA A G SNX11 Ensembl:ENSG00000002919 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917694871 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80932,RMVar_hsa_circ_294323,RMVar_hsa_circ_185081,RMVar_hsa_circ_185085,RMVar_hsa_circ_9124 39682 RMVar_ID_39682 Human_SNP_ID_626027690 A-to-I Human chr17 + 48116356 48116356 48116356 CTCCCACTTCAGCCTCCCAAGTAGCTGGGACTACAGGTATGTGCCACCATGCTCAGCTAATTTTT CTCCCACTTCAGCCTCCCAAGTAGCTGGGACTGCAGGTATGTGCCACCATGCTCAGCTAATTTTT A G SNX11 Ensembl:ENSG00000002919 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1272503191 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80932,RMVar_hsa_circ_294323,RMVar_hsa_circ_185081,RMVar_hsa_circ_185085,RMVar_hsa_circ_9124 39683 RMVar_ID_39683 Human_SNP_ID_626028046 A-to-I Human chr17 + 48117741 48117741 48117741 ACAACATAGTGTGGCTCGGCTTGGTGGCTCACACATGTAATTCCAGTGCTTTGGGAGGTTAAGGA ACAACATAGTGTGGCTCGGCTTGGTGGCTCACGCATGTAATTCCAGTGCTTTGGGAGGTTAAGGA A G SNX11 Ensembl:ENSG00000002919 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1471617598 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80932,RMVar_hsa_circ_294323,RMVar_hsa_circ_185081,RMVar_hsa_circ_185085,RMVar_hsa_circ_9124 39684 RMVar_ID_39684 Human_SNP_ID_626198911 A-to-I Human chr17 + 48842704 48842704 48842704 GTCTCATTGCCCAGGCTGAAGTACAGTGGTGCAATCTCGGCTCACTGCAACCCCCACCTCCCAGG GTCTCATTGCCCAGGCTGAAGTACAGTGGTGCGATCTCGGCTCACTGCAACCCCCACCTCCCAGG A G CALCOCO2 Ensembl:ENSG00000136436 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1396771504 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13220309,Human_RBP_ID_25336421 RMVar_hsa_circ_64515,RMVar_hsa_circ_69416 39685 RMVar_ID_39685 Human_SNP_ID_626199376 A-to-I Human chr17 + 48844792 48844792 48844792 CACCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCTACCGCGCCCGGCCAATCTGG CACCCACCTCAGCCTCCCAAAGTGCTGGGATTGCAGGCGTGAGCTACCGCGCCCGGCCAATCTGG A G CALCOCO2 Ensembl:ENSG00000136436 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1489495131 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64515,RMVar_hsa_circ_69416 39686 RMVar_ID_39686 Human_SNP_ID_626204723 A-to-I Human chr17 + 48864157 48864157 48864157 GCGCAGTTGACTCACTACAGCCTCTGCCTCCCAGGTTCAAGCGATTCTCATGCCTTAGCCTCCCA GCGCAGTTGACTCACTACAGCCTCTGCCTCCCGGGTTCAAGCGATTCTCATGCCTTAGCCTCCCA A G CALCOCO2 Ensembl:ENSG00000136436 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1309998275 Functional Loss SNV dbSNP153 33..33 33 - - - 39687 RMVar_ID_39687 Human_SNP_ID_626204743 A-to-I Human chr17 + 48864229 48864229 48864229 GGGATTACAGGTGTGTGCCGCAATGCCCAGCTAATTTTTGTGTTTTTAGTAGAGACAGGGTTTCA GGGATTACAGGTGTGTGCCGCAATGCCCAGCTGATTTTTGTGTTTTTAGTAGAGACAGGGTTTCA A G CALCOCO2 Ensembl:ENSG00000136436 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1239144284 Functional Loss SNV dbSNP153 33..33 33 - - - 39688 RMVar_ID_39688 Human_SNP_ID_626204763 A-to-I Human chr17 + 48864324 48864324 48864324 GGCCTCACGTGATCTGTCCACTTCAGCCGTCCAAAGTGCTGGGATTACAAGCGTGAGCCACTGTG GGCCTCACGTGATCTGTCCACTTCAGCCGTCCGAAGTGCTGGGATTACAAGCGTGAGCCACTGTG A G CALCOCO2 Ensembl:ENSG00000136436 Protein coding 3'UTR GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1195845987 Functional Loss SNV dbSNP153 33..33 33 - - - 39689 RMVar_ID_39689 Human_SNP_ID_626204954 A-to-I Human chr17 + 48865264 48865263 48865265 TAGTAGTAAACAATAGTTCTTTTTTTTGAGACAGAGTTTCACTCTGTCACCCAGGCTAGAGTGCA TAGTAGTAAACAATAGTTCTTTTTTTTGAGAC__AGTTTCACTCTGTCACCCAGGCTAGAGTGCA CAG C CALCOCO2 Ensembl:ENSG00000136436 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459821964 Functional Loss DEL dbSNP153 33..34 33 - - - 39690 RMVar_ID_39690 Human_SNP_ID_626205646 A-to-I Human chr17 + 48867453 48867453 48867453 GTGGTGGTGGGTGCCTGTAGTCTGGGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCCA GTGGTGGTGGGTGCCTGTAGTCTGGGCTACTCTGGAGGCTGAGGCAGGAGAATCACTTGAACCCA A T - - Other Unknown GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1406965911 Functional Loss SNV dbSNP153 33..33 33 - - - 39691 RMVar_ID_39691 Human_SNP_ID_626219265 A-to-I Human chr17 + 48917959 48917958 48917960 ACAGCTTAATTAATTTATTTATTTTTTGAGACAGAGTTTCACTATTGTTACCCAGGCTGGAGTGT ACAGCTTAATTAATTTATTTATTTTTTGAGAC__AGTTTCACTATTGTTACCCAGGCTGGAGTGT CAG C UBE2Z Ensembl:ENSG00000159202 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1460617434 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_13233634 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_60229,RMVar_hsa_circ_185108,RMVar_hsa_circ_78664,RMVar_hsa_circ_185111,RMVar_hsa_circ_109311,RMVar_hsa_circ_185109,RMVar_hsa_circ_40946,RMVar_hsa_circ_304645,RMVar_hsa_circ_287741,RMVar_hsa_circ_185112,RMVar_hsa_circ_185110 39692 RMVar_ID_39692 Human_SNP_ID_626220881 A-to-I Human chr17 + 48923509 48923509 48923509 AAAAAATTGGCTCAGCGTGGTAGCATGTGCCTATAATCCCGGCTACTTGGGAGGCTGAGGCAGGA AAAAAATTGGCTCAGCGTGGTAGCATGTGCCTGTAATCCCGGCTACTTGGGAGGCTGAGGCAGGA A G UBE2Z Ensembl:ENSG00000159202 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1162479581 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25297023 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_185118,RMVar_hsa_circ_78837 39693 RMVar_ID_39693 Human_SNP_ID_626220981 A-to-I Human chr17 + 48923826 48923826 48923826 TGGGTCACAGCTCACTGCAACTCCAAACTCCCAAGCTCAAGCAGTCCTCCCACCTCAGCCTCCCA TGGGTCACAGCTCACTGCAACTCCAAACTCCCGAGCTCAAGCAGTCCTCCCACCTCAGCCTCCCA A G UBE2Z Ensembl:ENSG00000159202 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs968836333 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17566921 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_185118,RMVar_hsa_circ_78837 39694 RMVar_ID_39694 Human_SNP_ID_626221158 A-to-I Human chr17 + 48924636 48924636 48924636 GGGAGGCAGAGGTGGACAGATCTCTTGAGGCCAGGAGTCCAAGACCAGCCTGGCCAACATGGTGA GGGAGGCAGAGGTGGACAGATCTCTTGAGGCCGGGAGTCCAAGACCAGCCTGGCCAACATGGTGA A G UBE2Z Ensembl:ENSG00000159202 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1278272574 Functional Loss SNV dbSNP153 33..33 33 - - - 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_185118,RMVar_hsa_circ_78837 39695 RMVar_ID_39695 Human_SNP_ID_626221161 A-to-I Human chr17 + 48924644 48924644 48924644 GAGGTGGACAGATCTCTTGAGGCCAGGAGTCCAAGACCAGCCTGGCCAACATGGTGAAACCCCAT GAGGTGGACAGATCTCTTGAGGCCAGGAGTCCGAGACCAGCCTGGCCAACATGGTGAAACCCCAT A G UBE2Z Ensembl:ENSG00000159202 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1302087324 Functional Loss SNV dbSNP153 33..33 33 - - - 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_185118,RMVar_hsa_circ_78837 39696 RMVar_ID_39696 Human_SNP_ID_626221169 A-to-I Human chr17 + 48924675 48924673 48924675 CAAGACCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCCAGGCA CAAGACCAGCCTGGCCAACATGGTGAAACCC__TCTCTACTAAAAATACAAAAATTAGCCAGGCA CCA C UBE2Z Ensembl:ENSG00000159202 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1472102963 Functional Loss DEL dbSNP153 32..33 33 - - - 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_185118,RMVar_hsa_circ_78837 39697 RMVar_ID_39697 Human_SNP_ID_626221256 A-to-I Human chr17 + 48924913 48924913 48924913 TAGACTAATGTAAACCACCTGGTTGGTAAGAGAATGAGAATTCTCCTGTCCTGGAGAATCAGTTC TAGACTAATGTAAACCACCTGGTTGGTAAGAGGATGAGAATTCTCCTGTCCTGGAGAATCAGTTC A G UBE2Z Ensembl:ENSG00000159202 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4239161 Functional Loss SNV dbSNP153 33..33 33 - - - 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_185118,RMVar_hsa_circ_78837 39698 RMVar_ID_39698 Human_SNP_ID_626221323 A-to-I Human chr17 + 48925176 48925176 48925176 GTAGTGGTGCGTGCCTGTGGTCCCAGCTACTTAGGAGACTGAGGCACAAGAATTTTGCTTGAACC GTAGTGGTGCGTGCCTGTGGTCCCAGCTACTTCGGAGACTGAGGCACAAGAATTTTGCTTGAACC A C UBE2Z Ensembl:ENSG00000159202 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1030251720 Functional Loss SNV dbSNP153 33..33 33 - - - 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_185118,RMVar_hsa_circ_78837 39699 RMVar_ID_39699 Human_SNP_ID_626221671 A-to-I Human chr17 + 48926506 48926506 48926506 CTTTTTTTTTTTTTTTTTTGAGACCAAGTTTTACTCTTGTTGCCCAGGCTGGAGTGTAATGGTGC CTTTTTTTTTTTTTTTTTTGAGACCAAGTTTTTCTCTTGTTGCCCAGGCTGGAGTGTAATGGTGC A T UBE2Z Ensembl:ENSG00000159202 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1202212451 Functional Loss SNV dbSNP153 33..33 33 - - - 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_185118,RMVar_hsa_circ_78837 39700 RMVar_ID_39700 Human_SNP_ID_626221683 A-to-I Human chr17 + 48926551 48926551 48926551 AGGCTGGAGTGTAATGGTGCGATCTCGATCTCAGCTGACTGCAACCTCCGCCTCCCGGGTTCAAG AGGCTGGAGTGTAATGGTGCGATCTCGATCTCCGCTGACTGCAACCTCCGCCTCCCGGGTTCAAG A C UBE2Z Ensembl:ENSG00000159202 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs914558000 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13056293 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_185118,RMVar_hsa_circ_78837 39701 RMVar_ID_39701 Human_SNP_ID_626221684 A-to-I Human chr17 + 48926551 48926551 48926551 AGGCTGGAGTGTAATGGTGCGATCTCGATCTCAGCTGACTGCAACCTCCGCCTCCCGGGTTCAAG AGGCTGGAGTGTAATGGTGCGATCTCGATCTCGGCTGACTGCAACCTCCGCCTCCCGGGTTCAAG A G UBE2Z Ensembl:ENSG00000159202 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs914558000 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13056293 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_185118,RMVar_hsa_circ_78837 39702 RMVar_ID_39702 Human_SNP_ID_626221707 A-to-I Human chr17 + 48926611 48926611 48926611 TCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCATGCGCCACGACACCCG TCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTGGCTGGGATTACAGGCATGCGCCACGACACCCG A G UBE2Z Ensembl:ENSG00000159202 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs895444274 Functional Loss SNV dbSNP153 33..33 33 - - - 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_185118,RMVar_hsa_circ_78837 39703 RMVar_ID_39703 Human_SNP_ID_626222543 A-to-I Human chr17 - 48929770 48929770 48929770 ACCCTGTGCCATTTTACATACAGCTCACTTAAATTTCACCAAGTAGGCAGCCTTCAACATCACAG ACCCTGTGCCATTTTACATACAGCTCACTTAAGTTTCACCAAGTAGGCAGCCTTCAACATCACAG T C SNF8 Ensembl:ENSG00000159210 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs532697870 Functional Loss SNV dbSNP153 33..33 33 - - - 39704 RMVar_ID_39704 Human_SNP_ID_626223914 A-to-I Human chr17 - 48934560 48934560 48934560 TTGCTCTGTTGTCTAGGCTGGAGCGCAGTGGTACAATCTCGGCTCACTGCAACCTCCGCCTCCTG TTGCTCTGTTGTCTAGGCTGGAGCGCAGTGGTGCAATCTCGGCTCACTGCAACCTCCGCCTCCTG T C SNF8 Ensembl:ENSG00000159210 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1234169628 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13220310 Human_Splice_Rec_1835188,Human_Splice_Rec_1835189 RMVar_hsa_circ_122023,RMVar_hsa_circ_185120 39705 RMVar_ID_39705 Human_SNP_ID_626225337 A-to-I Human chr17 - 48939358 48939356 48939358 TCAGCCCACTGCAGCCTTCAACTCCAGGGCTCAAGTTACTTTCCTGCCTCAACCTCCCAAGTGGA TCAGCCCACTGCAGCCTTCAACTCCAGGGCTC__GTTACTTTCCTGCCTCAACCTCCCAAGTGGA CTT C SNF8 Ensembl:ENSG00000159210 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879671063 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_13056845 RMVar_hsa_circ_91459,RMVar_hsa_circ_185121 39706 RMVar_ID_39706 Human_SNP_ID_626225337 A-to-I Human chr17 - 48939357 48939356 48939358 CAGCCCACTGCAGCCTTCAACTCCAGGGCTCAAGTTACTTTCCTGCCTCAACCTCCCAAGTGGAG CAGCCCACTGCAGCCTTCAACTCCAGGGCTC__GTTACTTTCCTGCCTCAACCTCCCAAGTGGAG CTT C SNF8 Ensembl:ENSG00000159210 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879671063 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_13056845 RMVar_hsa_circ_91459,RMVar_hsa_circ_185121 39707 RMVar_ID_39707 Human_SNP_ID_626225587 A-to-I Human chr17 - 48940181 48940181 48940181 TAAAAATTTGCCAGGTGTGGTGGCATGTGTCTATAGTCCAGCTACTCGGGAGGCTAAGGTGGGAG TAAAAATTTGCCAGGTGTGGTGGCATGTGTCTGTAGTCCAGCTACTCGGGAGGCTAAGGTGGGAG T C SNF8 Ensembl:ENSG00000159210 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1385612100 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91459,RMVar_hsa_circ_185121 39708 RMVar_ID_39708 Human_SNP_ID_626248949 A-to-I Human chr17 + 49024329 49024329 49024329 AGCTATACAGGAGGGTGGGAGCTGGGAGGATCACTCGATCGCAGCAGGTCTAGGCTGCAGTGAGC AGCTATACAGGAGGGTGGGAGCTGGGAGGATCCCTCGATCGCAGCAGGTCTAGGCTGCAGTGAGC A C IGF2BP1 Ensembl:ENSG00000159217 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1044921026 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3527222,Human_RBP_ID_13220313 RMVar_hsa_circ_104939,RMVar_hsa_circ_86147,RMVar_hsa_circ_185123,RMVar_hsa_circ_185124 39709 RMVar_ID_39709 Human_SNP_ID_626250164 A-to-I Human chr17 + 49028069 49028069 49028069 CCTGCAGTCCCAGTCACTAGGGAGGCTGAGGCAAGAGGATTGCTGGAGCCCAGGAGGCCAAGGCT CCTGCAGTCCCAGTCACTAGGGAGGCTGAGGCGAGAGGATTGCTGGAGCCCAGGAGGCCAAGGCT A G IGF2BP1 Ensembl:ENSG00000159217 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569937508 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17565996 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_300782,RMVar_hsa_circ_185125,RMVar_hsa_circ_185126,RMVar_hsa_circ_185128,RMVar_hsa_circ_92889 39710 RMVar_ID_39710 Human_SNP_ID_626253427 A-to-I Human chr17 + 49040345 49040345 49040345 TCAAGGGATCCTCCCGCCTCAGCCTTCTGAGTAGCTAGGACAACATGCATGCACCACCACGCCTG TCAAGGGATCCTCCCGCCTCAGCCTTCTGAGTGGCTAGGACAACATGCATGCACCACCACGCCTG A G IGF2BP1 Ensembl:ENSG00000159217 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1302682916 Functional Loss SNV dbSNP153 33..33 33 - - - 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_76622,RMVar_hsa_circ_185128,RMVar_hsa_circ_92889,RMVar_hsa_circ_10829,RMVar_hsa_circ_113312,RMVar_hsa_circ_185129,RMVar_hsa_circ_45562,RMVar_hsa_circ_97241,RMVar_hsa_circ_185130,RMVar_hsa_circ_185131 39711 RMVar_ID_39711 Human_SNP_ID_626253428 A-to-I Human chr17 + 49040349 49040349 49040349 GGGATCCTCCCGCCTCAGCCTTCTGAGTAGCTAGGACAACATGCATGCACCACCACGCCTGCCTA GGGATCCTCCCGCCTCAGCCTTCTGAGTAGCTGGGACAACATGCATGCACCACCACGCCTGCCTA A G IGF2BP1 Ensembl:ENSG00000159217 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1197577669 Functional Loss SNV dbSNP153 33..33 33 - - - 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_76622,RMVar_hsa_circ_185128,RMVar_hsa_circ_92889,RMVar_hsa_circ_10829,RMVar_hsa_circ_113312,RMVar_hsa_circ_185129,RMVar_hsa_circ_45562,RMVar_hsa_circ_97241,RMVar_hsa_circ_185130,RMVar_hsa_circ_185131 39712 RMVar_ID_39712 Human_SNP_ID_626298660 A-to-I Human chr17 + 49221066 49221066 49221066 GTGGTGGTGCGTGCCTGTAATTCCAGCTACTCAGGAGGCTGAGGCAGGAGGATCACTTGAACCCA GTGGTGGTGCGTGCCTGTAATTCCAGCTACTCGGGAGGCTGAGGCAGGAGGATCACTTGAACCCA A G ABI3 Ensembl:ENSG00000108798 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1286400273 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95809,RMVar_hsa_circ_103092,RMVar_hsa_circ_86979,RMVar_hsa_circ_185142,RMVar_hsa_circ_185143,RMVar_hsa_circ_92942,RMVar_hsa_circ_185144,RMVar_hsa_circ_185145 39713 RMVar_ID_39713 Human_SNP_ID_626328200 A-to-I Human chr17 - 49334522 49334522 49334522 CACCTGCCTTAGCCTCCCGTAGTTCTGGGATTACAGGCCTAAGTCACCATGCCCGGCCATTTCTT CACCTGCCTTAGCCTCCCGTAGTTCTGGGATTGCAGGCCTAAGTCACCATGCCCGGCCATTTCTT T C ZNF652 Ensembl:ENSG00000198740 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1291257136 Functional Loss SNV dbSNP153 33..33 33 - - - 39714 RMVar_ID_39714 Human_SNP_ID_626328206 A-to-I Human chr17 - 49334557 49334557 49334557 CCACGCTGGTCTCGAACTCCTGAACTCTAGCAATTCACCTGCCTTAGCCTCCCGTAGTTCTGGGA CCACGCTGGTCTCGAACTCCTGAACTCTAGCAGTTCACCTGCCTTAGCCTCCCGTAGTTCTGGGA T C ZNF652 Ensembl:ENSG00000198740 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749652228 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13058825 39715 RMVar_ID_39715 Human_SNP_ID_626329600 A-to-I Human chr17 - 49339487 49339487 49339487 CTGGCTAGTGCCACGAGGTTTACTTGACTGTTATGTGAAAAGCTGATAAGAAAACCATCCAGAAA CTGGCTAGTGCCACGAGGTTTACTTGACTGTTGTGTGAAAAGCTGATAAGAAAACCATCCAGAAA T C ZNF652 Ensembl:ENSG00000198740 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878946071 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1182728,Human_RBP_ID_3527358,Human_RBP_ID_4436643,Human_RBP_ID_8455929,Human_RBP_ID_13058898,Human_RBP_ID_26460708,Human_RBP_ID_26965455 39716 RMVar_ID_39716 Human_SNP_ID_626329664 A-to-I Human chr17 - 49339729 49339729 49339729 CGGAGCAGCTCTGTGAAGATGCAAAAATACACAAAAAAAATTCCAGAACATCTGGGAGAATATTT CGGAGCAGCTCTGTGAAGATGCAAAAATACACGAAAAAAATTCCAGAACATCTGGGAGAATATTT T C ZNF652 Ensembl:ENSG00000198740 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs879130796 Functional Loss SNV dbSNP153 33..33 33 - - - 39717 RMVar_ID_39717 Human_SNP_ID_626329757 A-to-I Human chr17 - 49339986 49339986 49339986 GGCTCACGCCTGTAATCCCGGCACTTTGAGAAACAGAGGCAGGTGGATCACGAGGTCAGGAGTTC GGCTCACGCCTGTAATCCCGGCACTTTGAGAAGCAGAGGCAGGTGGATCACGAGGTCAGGAGTTC T C ZNF652 Ensembl:ENSG00000198740 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1336766442 Functional Loss SNV dbSNP153 33..33 33 - - - 39718 RMVar_ID_39718 Human_SNP_ID_626330779 A-to-I Human chr17 - 49343837 49343837 49343837 TTGCCGAGGCTGGTCTTGAACTCTGGGCCTCAAGCAATCCTCGCACTTTGGCCTGCCAAAGTTTT TTGCCGAGGCTGGTCTTGAACTCTGGGCCTCAGGCAATCCTCGCACTTTGGCCTGCCAAAGTTTT T C ZNF652 Ensembl:ENSG00000198740 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs986970409 Functional Loss SNV dbSNP153 33..33 33 - - - 39719 RMVar_ID_39719 Human_SNP_ID_626330926 A-to-I Human chr17 - 49344249 49344249 49344249 GTGATCCTCCTGCCTCAGTTTCTCAAGTAGCTAGGACTATAGGCATGCACCACCATACCTAGCTA GTGATCCTCCTGCCTCAGTTTCTCAAGTAGCTGGGACTATAGGCATGCACCACCATACCTAGCTA T C ZNF652 Ensembl:ENSG00000198740 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs531103427 Functional Loss SNV dbSNP153 33..33 33 - - - 39720 RMVar_ID_39720 Human_SNP_ID_626337763 A-to-I Human chr17 + 49369341 49369341 49369341 ATCCCACCTCAGCCTCCCAAGTAGCTGGGACTACAGGCACACACCACCACATCTGGCTAATTCTT ATCCCACCTCAGCCTCCCAAGTAGCTGGGACTGCAGGCACACACCACCACATCTGGCTAATTCTT A G AC091180.3 Ensembl:ENSG00000248714 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs930914971 Functional Loss SNV dbSNP153 33..33 33 - - - 39721 RMVar_ID_39721 Human_SNP_ID_626395997 A-to-I Human chr17 - 49602462 49602462 49602462 GGGATTGCAGTAAATAAGGGATTTCACAGGGTAGACACCAATTCTTTCACCCTTCCCCACAGATC GGGATTGCAGTAAATAAGGGATTTCACAGGGTGGACACCAATTCTTTCACCCTTCCCCACAGATC T C SPOP Ensembl:ENSG00000121067 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs370935632 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13060094 39722 RMVar_ID_39722 Human_SNP_ID_626396113 A-to-I Human chr17 - 49603120 49603120 49603120 CAGATATGCCTCCTCACCCAGAATTCATAACAATTAAATTGTCCTGATTTGATTGCCATGATTCA CAGATATGCCTCCTCACCCAGAATTCATAACAGTTAAATTGTCCTGATTTGATTGCCATGATTCA T C SPOP Ensembl:ENSG00000121067 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs568782956 Functional Loss SNV dbSNP153 33..33 33 - - - 39723 RMVar_ID_39723 Human_SNP_ID_626396435 A-to-I Human chr17 - 49604735 49604735 49604735 TCTGTGGAAACATGACCTGTGGGGAAGGGTGAAAGAATTGGTGTTTACCCTGTGGGAGCTTTTCC TCTGTGGAAACATGACCTGTGGGGAAGGGTGACAGAATTGGTGTTTACCCTGTGGGAGCTTTTCC T G SPOP Ensembl:ENSG00000121067 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1199793691 Functional Loss SNV dbSNP153 33..33 33 - - - 39724 RMVar_ID_39724 Human_SNP_ID_626396615 A-to-I Human chr17 - 49605614 49605614 49605614 ACAATCTCGGCTCACTGCAACCTCCGCCTCCCAGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCCG ACAATCTCGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCCG T C SPOP Ensembl:ENSG00000121067 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs912928042 Functional Loss SNV dbSNP153 33..33 33 - - - 39725 RMVar_ID_39725 Human_SNP_ID_626412596 A-to-I Human chr17 - 49675968 49675968 49675968 TCACCCAGGCTGGAGTGCAGTGGCGCGATCTCAGCTCACTGCCACCTTTGCCTCCTGGGTTCAAG TCACCCAGGCTGGAGTGCAGTGGCGCGATCTCGGCTCACTGCCACCTTTGCCTCCTGGGTTCAAG T C SPOP Ensembl:ENSG00000121067 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs995692146 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1835918,Human_Splice_Rec_1835919,Human_Splice_Rec_1835958,Human_Splice_Rec_1835959,Human_Splice_Rec_1835982,Human_Splice_Rec_1835983,Human_Splice_Rec_1836158,Human_Splice_Rec_1836159,Human_Splice_Rec_1836202,Human_Splice_Rec_1836203,Human_Splice_Rec_1836210,Human_Splice_Rec_1836211 39726 RMVar_ID_39726 Human_SNP_ID_626421930 A-to-I Human chr17 - 49712030 49712030 49712030 GTGATTCTCCTGCCTCAGCCTTCTGAATAGCTAGGATTACAGGAGCATGCTGCCACACCCGGCTA GTGATTCTCCTGCCTCAGCCTTCTGAATAGCTGGGATTACAGGAGCATGCTGCCACACCCGGCTA T C FAM117A Ensembl:ENSG00000121104 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1006348927 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_185177,RMVar_hsa_circ_84222 39727 RMVar_ID_39727 Human_SNP_ID_626421936 A-to-I Human chr17 - 49712064 49712064 49712064 TTGGCTTACTGCAACCTCCGCCTCCCAGGTTCAAGTGATTCTCCTGCCTCAGCCTTCTGAATAGC TTGGCTTACTGCAACCTCCGCCTCCCAGGTTCGAGTGATTCTCCTGCCTCAGCCTTCTGAATAGC T C FAM117A Ensembl:ENSG00000121104 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1180151837 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_185177,RMVar_hsa_circ_84222 39728 RMVar_ID_39728 Human_SNP_ID_626425286 A-to-I Human chr17 - 49726361 49726358 49726362 CTACAAATACAAAATTAGCCAGGTGTGGTGGCACATGCCTGTAATCCCAGCTACTTGGGAGGCTG CTACAAATACAAAATTAGCCAGGTGTGGTGG____TGCCTGTAATCCCAGCTACTTGGGAGGCTG ATGTG A FAM117A Ensembl:ENSG00000121104 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1209015449 Functional Loss DEL dbSNP153 32..35 33 - - - RMVar_hsa_circ_42007 39729 RMVar_ID_39729 Human_SNP_ID_626427430 A-to-I Human chr17 - 49736434 49736434 49736434 GAGACCATGGTGAAACCCTGTCTCTACTAAAAATACAAAAAAATTAGCCGGGCATGGTGGTGGGT GAGACCATGGTGAAACCCTGTCTCTACTAAAACTACAAAAAAATTAGCCGGGCATGGTGGTGGGT T G FAM117A Ensembl:ENSG00000121104 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1181675856 Functional Loss SNV dbSNP153 33..33 33 - - - 39730 RMVar_ID_39730 Human_SNP_ID_626449653 A-to-I Human chr17 + 49830230 49830230 49830230 TTTTTTTTTTTAAAAAAAGACAGTCTCACTCTATCATCCAGTCCGGAATGCAGTGGCATGATCTC TTTTTTTTTTTAAAAAAAGACAGTCTCACTCTGTCATCCAGTCCGGAATGCAGTGGCATGATCTC A G KAT7 Ensembl:ENSG00000136504 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs530952560 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6610239,Human_RBP_ID_13062824 39731 RMVar_ID_39731 Human_SNP_ID_626449664 A-to-I Human chr17 + 49830258 49830258 49830258 CTCTATCATCCAGTCCGGAATGCAGTGGCATGATCTCAGCTCACTGCAATGTCTGCCTCCTGGAT CTCTATCATCCAGTCCGGAATGCAGTGGCATGGTCTCAGCTCACTGCAATGTCTGCCTCCTGGAT A G KAT7 Ensembl:ENSG00000136504 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037975856 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13062824 39732 RMVar_ID_39732 Human_SNP_ID_626450092 A-to-I Human chr17 + 49831987 49831987 49831987 AGCCATTTTTTTTTTTTTTAAGACGACGTCTCACTCTGTCACCTATGCTGGAGTGCAGTGGCGTG AGCCATTTTTTTTTTTTTTAAGACGACGTCTCGCTCTGTCACCTATGCTGGAGTGCAGTGGCGTG A G KAT7 Ensembl:ENSG00000136504 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1273094744 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13062915 39733 RMVar_ID_39733 Human_SNP_ID_626450110 A-to-I Human chr17 + 49832055 49832055 49832055 TAGGCTCATTGCAACCTCTGCCTCCCAGGTTCAAGCGATTTTCCTGCCTCAGCCTCCCAAGTAGC TAGGCTCATTGCAACCTCTGCCTCCCAGGTTCGAGCGATTTTCCTGCCTCAGCCTCCCAAGTAGC A G KAT7 Ensembl:ENSG00000136504 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs747107085 Functional Loss SNV dbSNP153 33..33 33 - - - 39734 RMVar_ID_39734 Human_SNP_ID_626450824 A-to-I Human chr17 + 49834883 49834883 49834883 AAAATTAGTTGGGCATGGTGGTGTGCACCCGTAGTGCCAGCTACTCAGGAGGCTGAGGTAGGAGG AAAATTAGTTGGGCATGGTGGTGTGCACCCGTGGTGCCAGCTACTCAGGAGGCTGAGGTAGGAGG A G KAT7,AC027801.5 Ensembl:ENSG00000136504,Ensembl:ENSG00000262837 Protein coding,lincRNA 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1411955973 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3548198,Human_RBP_ID_5248305 39735 RMVar_ID_39735 Human_SNP_ID_626476595 A-to-I Human chr17 - 49939139 49939139 49939139 TTGGCAGTTTTGGTTAAGGAGACTTTCTTGTCACACTTGGATTTGGGCATTGCACTGAATCCACG TTGGCAGTTTTGGTTAAGGAGACTTTCTTGTCGCACTTGGATTTGGGCATTGCACTGAATCCACG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1369545107 Functional Loss SNV dbSNP153 33..33 33 - - - 39736 RMVar_ID_39736 Human_SNP_ID_626515690 A-to-I Human chr17 + 50082304 50082304 50082304 TGGTTCATGCCATTCTCCTGCCTTGGCCTCCCAAGTAGCTGGGACTACAGGCGCCCACCACCACG TGGTTCATGCCATTCTCCTGCCTTGGCCTCCCGAGTAGCTGGGACTACAGGCGCCCACCACCACG A G ITGA3 Ensembl:ENSG00000005884 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1336251894 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_79347,RMVar_hsa_circ_185230,RMVar_hsa_circ_109370,RMVar_hsa_circ_185237,RMVar_hsa_circ_371582,RMVar_hsa_circ_185239,RMVar_hsa_circ_185240,RMVar_hsa_circ_104957,RMVar_hsa_circ_185241 39737 RMVar_ID_39737 Human_SNP_ID_626516042 A-to-I Human chr17 + 50084047 50084047 50084047 TCATTTGAGTTCAGTTCGAGACTAGCCTGGGCAACATGGTGAAACCCCATCTGTATTAAAAATAC TCATTTGAGTTCAGTTCGAGACTAGCCTGGGCGACATGGTGAAACCCCATCTGTATTAAAAATAC A G ITGA3 Ensembl:ENSG00000005884 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1419370049 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_79347,RMVar_hsa_circ_185230,RMVar_hsa_circ_109370,RMVar_hsa_circ_185237,RMVar_hsa_circ_371582,RMVar_hsa_circ_185239,RMVar_hsa_circ_185240,RMVar_hsa_circ_104957,RMVar_hsa_circ_185241 39738 RMVar_ID_39738 Human_SNP_ID_626516402 A-to-I Human chr17 + 50085570 50085570 50085570 CCTGTAATCTCAGAAACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAGCCCAGGAGGCAGAGGTT CCTGTAATCTCAGAAACTCAGGAGGCTGAGGCGGGAGAATTGCTTGAGCCCAGGAGGCAGAGGTT A G ITGA3 Ensembl:ENSG00000005884 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs998728652 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_79347,RMVar_hsa_circ_185230,RMVar_hsa_circ_109370,RMVar_hsa_circ_185237,RMVar_hsa_circ_371582,RMVar_hsa_circ_185239,RMVar_hsa_circ_185240,RMVar_hsa_circ_104957,RMVar_hsa_circ_185241 39739 RMVar_ID_39739 Human_SNP_ID_626542153 A-to-I Human chr17 + 50179665 50179665 50179665 ACCTCAGGCAATACGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTAGAGGCGTGAGCCACCGCCC ACCTCAGGCAATACGCCCGCCTCGGCCTCCCAGAGTGCTGGGATTAGAGGCGTGAGCCACCGCCC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1046630282 Functional Loss SNV dbSNP153 33..33 33 - - - 39740 RMVar_ID_39740 Human_SNP_ID_626577102 A-to-I Human chr17 - 50308698 50308698 50308698 TTGCTCAGGCTGGAGTGCCATGACATGATCTCAGCTCGCTGTAGCCTCTGCCTCCCAGGTTCAAG TTGCTCAGGCTGGAGTGCCATGACATGATCTCCGCTCGCTGTAGCCTCTGCCTCCCAGGTTCAAG T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1000798422 Functional Loss SNV dbSNP153 33..33 33 - - - 39741 RMVar_ID_39741 Human_SNP_ID_626596338 A-to-I Human chr17 - 50384657 50384657 50384657 GGGTTCAAGAGATTCTCTTGCCTCAACCTCCAAAGTAGCTGGGATTACAGGCATGTGCCACCACG GGGTTCAAGAGATTCTCTTGCCTCAACCTCCAGAGTAGCTGGGATTACAGGCATGTGCCACCACG T C LRRC59 Ensembl:ENSG00000108829 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs951807156 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113694,RMVar_hsa_circ_185326,RMVar_hsa_circ_89200,RMVar_hsa_circ_100239,RMVar_hsa_circ_185327,RMVar_hsa_circ_185328 39742 RMVar_ID_39742 Human_SNP_ID_626596340 A-to-I Human chr17 - 50384664 50384664 50384664 GTCTCCTGGGTTCAAGAGATTCTCTTGCCTCAACCTCCAAAGTAGCTGGGATTACAGGCATGTGC GTCTCCTGGGTTCAAGAGATTCTCTTGCCTCAGCCTCCAAAGTAGCTGGGATTACAGGCATGTGC T C LRRC59 Ensembl:ENSG00000108829 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs984435607 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113694,RMVar_hsa_circ_185326,RMVar_hsa_circ_89200,RMVar_hsa_circ_100239,RMVar_hsa_circ_185327,RMVar_hsa_circ_185328 39743 RMVar_ID_39743 Human_SNP_ID_626607339 A-to-I Human chr17 + 50428697 50428668 50428697 CCAGCTACTTGGGAGGCTGAGGCAGGAGAATTACTTGAACCTGGGAAGCGGAGGTTGCACTGAGC CCAG_____________________________CTTGAACCTGGGAAGCGGAGGTTGCACTGAGC GCTACTTGGGAGGCTGAGGCAGGAGAATTA G ACSF2 Ensembl:ENSG00000167107 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1343455006 Functional Loss DEL dbSNP153 5..33 33 - - - 39744 RMVar_ID_39744 Human_SNP_ID_626612468 A-to-I Human chr17 + 50451032 50451032 50451032 GTAGCTCGCTGTAGCCTCGACCTCTCAGGCTCAAGTGATCCTTCAGAGTAGCTAGGCCTCCGGAG GTAGCTCGCTGTAGCCTCGACCTCTCAGGCTCCAGTGATCCTTCAGAGTAGCTAGGCCTCCGGAG A C ACSF2 Ensembl:ENSG00000167107 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1486910061 Functional Loss SNV dbSNP153 33..33 33 - - - 39745 RMVar_ID_39745 Human_SNP_ID_626664260 A-to-I Human chr17 + 50635822 50635822 50635822 GGAGGATCACTTCAGCCCAGGAGTTTTAGATTACTGTGAGCTATGATCGCACCACTGCACTGTGG GGAGGATCACTTCAGCCCAGGAGTTTTAGATTGCTGTGAGCTATGATCGCACCACTGCACTGTGG A G ABCC3 Ensembl:ENSG00000108846 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs902038765 Functional Loss SNV dbSNP153 33..33 33 - - - 39746 RMVar_ID_39746 Human_SNP_ID_626665179 A-to-I Human chr17 + 50639984 50639984 50639984 CGGGGTTTCACCATGATGGCCAGGCTGGTCTCAAATTCCTGACCTCAAGTCATCTGCCCACCTCA CGGGGTTTCACCATGATGGCCAGGCTGGTCTCCAATTCCTGACCTCAAGTCATCTGCCCACCTCA A C ABCC3 Ensembl:ENSG00000108846 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs182734775 Functional Loss SNV dbSNP153 33..33 33 - - - 39747 RMVar_ID_39747 Human_SNP_ID_626665337 A-to-I Human chr17 + 50640723 50640723 50640723 TTAAATATTTTTAGTAGAGACAGCGTTTCGTCATGTTGGCCAGGCTGGTCGCAGACTCCTGACCT TTAAATATTTTTAGTAGAGACAGCGTTTCGTCGTGTTGGCCAGGCTGGTCGCAGACTCCTGACCT A G ABCC3 Ensembl:ENSG00000108846 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1001357447 Functional Loss SNV dbSNP153 33..33 33 - - - 39748 RMVar_ID_39748 Human_SNP_ID_626665338 A-to-I Human chr17 + 50640723 50640723 50640723 TTAAATATTTTTAGTAGAGACAGCGTTTCGTCATGTTGGCCAGGCTGGTCGCAGACTCCTGACCT TTAAATATTTTTAGTAGAGACAGCGTTTCGTCTTGTTGGCCAGGCTGGTCGCAGACTCCTGACCT A T ABCC3 Ensembl:ENSG00000108846 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1001357447 Functional Loss SNV dbSNP153 33..33 33 - - - 39749 RMVar_ID_39749 Human_SNP_ID_626665593 A-to-I Human chr17 + 50641892 50641892 50641892 ACATAGTGGGACCCCATCTCTACAAAAAAATTAAAAAATTAGCTGGGCGTGGTGGCACATGCCTG ACATAGTGGGACCCCATCTCTACAAAAAAATTTAAAAATTAGCTGGGCGTGGTGGCACATGCCTG A T ABCC3 Ensembl:ENSG00000108846 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027889558 Functional Loss SNV dbSNP153 33..33 33 - - - 39750 RMVar_ID_39750 Human_SNP_ID_626667001 A-to-I Human chr17 + 50647546 50647546 50647546 ACTCCTCAGGACAATCTGTGAACAATGATGAGAGAGAGCACCAAGGACCAAGGTCTGAACTTGGG ACTCCTCAGGACAATCTGTGAACAATGATGAGTGAGAGCACCAAGGACCAAGGTCTGAACTTGGG A T ABCC3 Ensembl:ENSG00000108846 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006725407 Functional Loss SNV dbSNP153 33..33 33 - - - 39751 RMVar_ID_39751 Human_SNP_ID_626667270 A-to-I Human chr17 + 50648689 50648689 50648689 CAGTAGCTGTTTCTTGGTCCTTGGTCCTTGGTACTCTCACTCATCATTGTTCACAGATTGCCCTG CAGTAGCTGTTTCTTGGTCCTTGGTCCTTGGTCCTCTCACTCATCATTGTTCACAGATTGCCCTG A C ABCC3 Ensembl:ENSG00000108846 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs533172003 Functional Loss SNV dbSNP153 33..33 33 - - - 39752 RMVar_ID_39752 Human_SNP_ID_626667271 A-to-I Human chr17 + 50648689 50648689 50648689 CAGTAGCTGTTTCTTGGTCCTTGGTCCTTGGTACTCTCACTCATCATTGTTCACAGATTGCCCTG CAGTAGCTGTTTCTTGGTCCTTGGTCCTTGGTGCTCTCACTCATCATTGTTCACAGATTGCCCTG A G ABCC3 Ensembl:ENSG00000108846 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs533172003 Functional Loss SNV dbSNP153 33..33 33 - - - 39753 RMVar_ID_39753 Human_SNP_ID_626667782 A-to-I Human chr17 + 50650881 50650881 50650881 GAGGGCAGAAGTTCAAGACCGGCCTGGCTGACATGCTGAAACCCTGTCTCTATTAAAAATACAAA GAGGGCAGAAGTTCAAGACCGGCCTGGCTGACGTGCTGAAACCCTGTCTCTATTAAAAATACAAA A G ABCC3 Ensembl:ENSG00000108846 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs373800814 Functional Loss SNV dbSNP153 33..33 33 - - - 39754 RMVar_ID_39754 Human_SNP_ID_626667783 A-to-I Human chr17 + 50650888 50650888 50650888 GAAGTTCAAGACCGGCCTGGCTGACATGCTGAAACCCTGTCTCTATTAAAAATACAAAAATTGGC GAAGTTCAAGACCGGCCTGGCTGACATGCTGAGACCCTGTCTCTATTAAAAATACAAAAATTGGC A G ABCC3 Ensembl:ENSG00000108846 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs543240077 Functional Loss SNV dbSNP153 33..33 33 - - - 39755 RMVar_ID_39755 Human_SNP_ID_626673570 A-to-I Human chr17 + 50671924 50671924 50671924 TTTGTATTTTTAGTAGAGATGGGTTTCACCATATTGGCCATGCTGGTCTTGAACTCCTGACTTCA TTTGTATTTTTAGTAGAGATGGGTTTCACCATGTTGGCCATGCTGGTCTTGAACTCCTGACTTCA A G ABCC3 Ensembl:ENSG00000108846 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1296737560 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1502,RMVar_hsa_circ_98270,RMVar_hsa_circ_124207,RMVar_hsa_circ_185356,RMVar_hsa_circ_185357,RMVar_hsa_circ_126145,RMVar_hsa_circ_185362,RMVar_hsa_circ_115604,RMVar_hsa_circ_84884,RMVar_hsa_circ_93926,RMVar_hsa_circ_185365,RMVar_hsa_circ_185366,RMVar_hsa_circ_114226,RMVar_hsa_circ_185367,RMVar_hsa_circ_105356,RMVar_hsa_circ_185368,RMVar_hsa_circ_185369 39756 RMVar_ID_39756 Human_SNP_ID_626673740 A-to-I Human chr17 + 50672586 50672586 50672586 ATAGATTCAGAAGACTGCTGTTCTGGTCAGGCACAGTGGCTCACACCTGTAATCCCAGCACTTTA ATAGATTCAGAAGACTGCTGTTCTGGTCAGGCGCAGTGGCTCACACCTGTAATCCCAGCACTTTA A G ABCC3 Ensembl:ENSG00000108846 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1443974506 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1502,RMVar_hsa_circ_98270,RMVar_hsa_circ_124207,RMVar_hsa_circ_185356,RMVar_hsa_circ_185357,RMVar_hsa_circ_126145,RMVar_hsa_circ_185362,RMVar_hsa_circ_115604,RMVar_hsa_circ_84884,RMVar_hsa_circ_93926,RMVar_hsa_circ_185365,RMVar_hsa_circ_185366,RMVar_hsa_circ_114226,RMVar_hsa_circ_185367,RMVar_hsa_circ_105356,RMVar_hsa_circ_185368,RMVar_hsa_circ_185369 39757 RMVar_ID_39757 Human_SNP_ID_626682637 A-to-I Human chr17 - 50705736 50705736 50705736 GAATCACTTGAACCAGGGAGTTGGAGGTTGAAATGAGCCAAGATCACACCACTGCACTCCAGGCT GAATCACTTGAACCAGGGAGTTGGAGGTTGAAGTGAGCCAAGATCACACCACTGCACTCCAGGCT T C ANKRD40 Ensembl:ENSG00000154945 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs933360064 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13067280 RMVar_hsa_circ_88427,RMVar_hsa_circ_185373 39758 RMVar_ID_39758 Human_SNP_ID_626682683 A-to-I Human chr17 - 50705901 50705901 50705901 TAATCTCAGCACTTTGGGAGGCCAAGGTGGGCAGATCACGATGTCAGGAGTTCGAGACCATTCTG TAATCTCAGCACTTTGGGAGGCCAAGGTGGGCGGATCACGATGTCAGGAGTTCGAGACCATTCTG T C ANKRD40 Ensembl:ENSG00000154945 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1380877095 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88427,RMVar_hsa_circ_185373 39759 RMVar_ID_39759 Human_SNP_ID_626682693 A-to-I Human chr17 - 50705932 50705932 50705932 TACCTGGACCTGGCGCGGTGGCTGACGCCTGTAATCTCAGCACTTTGGGAGGCCAAGGTGGGCAG TACCTGGACCTGGCGCGGTGGCTGACGCCTGTGATCTCAGCACTTTGGGAGGCCAAGGTGGGCAG T C ANKRD40 Ensembl:ENSG00000154945 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1357209806 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13067281 RMVar_hsa_circ_88427,RMVar_hsa_circ_185373 39760 RMVar_ID_39760 Human_SNP_ID_626687187 A-to-I Human chr17 + 50722302 50722302 50722302 TCATTGCACCCTCCGCCTCCCGGGTTCAAGCGATTCTCCTGCTTCAGCCTCCCCAGTAGCTGGAA TCATTGCACCCTCCGCCTCCCGGGTTCAAGCGGTTCTCCTGCTTCAGCCTCCCCAGTAGCTGGAA A G LUC7L3,AC005921.4 Ensembl:ENSG00000108848,Ensembl:ENSG00000278963 Protein coding,Other intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1382235731 Functional Loss SNV dbSNP153 33..33 33 - - - 39761 RMVar_ID_39761 Human_SNP_ID_626687846 A-to-I Human chr17 + 50724291 50724291 50724291 CACCTGTAATCTCAACATTGGGAGGCCAAGGCAGGCAGATCACTTGAGGCCAGGAGTTCGAGACC CACCTGTAATCTCAACATTGGGAGGCCAAGGCGGGCAGATCACTTGAGGCCAGGAGTTCGAGACC A G LUC7L3 Ensembl:ENSG00000108848 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs575334304 Functional Loss SNV dbSNP153 33..33 33 - - - 39762 RMVar_ID_39762 Human_SNP_ID_626687851 A-to-I Human chr17 + 50724321 50724321 50724321 GCAGGCAGATCACTTGAGGCCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCTGTCTC GCAGGCAGATCACTTGAGGCCAGGAGTTCGAGTCCAGCCTGGCCAACATGGTGAAACCCTGTCTC A T LUC7L3 Ensembl:ENSG00000108848 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1366509791 Functional Loss SNV dbSNP153 33..33 33 - - - 39763 RMVar_ID_39763 Human_SNP_ID_626687875 A-to-I Human chr17 + 50724384 50724384 50724384 TCTAATAAAAAATAAAAAAATTAGCTGGGCGTAGTGGTGCATTCCTGTAATCCCAGCTACTCTGG TCTAATAAAAAATAAAAAAATTAGCTGGGCGTGGTGGTGCATTCCTGTAATCCCAGCTACTCTGG A G LUC7L3 Ensembl:ENSG00000108848 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs540290703 Functional Loss SNV dbSNP153 33..33 33 - - - 39764 RMVar_ID_39764 Human_SNP_ID_626688096 A-to-I Human chr17 + 50724944 50724944 50724944 CCACCATGCCTGACTAATTTTTGTGTTGTTGTAGAGATGGGGTTTCACCATGTTTGCCGGGCTGG CCACCATGCCTGACTAATTTTTGTGTTGTTGTGGAGATGGGGTTTCACCATGTTTGCCGGGCTGG A G LUC7L3 Ensembl:ENSG00000108848 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1012796146 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3527936,Human_RBP_ID_6611781,Human_RBP_ID_8253518,Human_RBP_ID_18513717 39765 RMVar_ID_39765 Human_SNP_ID_626689769 A-to-I Human chr17 + 50729993 50729993 50729993 GTGGGGAGGTGGGGACAGTGTCTGGCTCTGTTACCCAGGCTGGAGTGCAGTGGCACAATCTCAGC GTGGGGAGGTGGGGACAGTGTCTGGCTCTGTTTCCCAGGCTGGAGTGCAGTGGCACAATCTCAGC A T LUC7L3 Ensembl:ENSG00000108848 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027054238 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17566007,Human_RBP_ID_26782425 39766 RMVar_ID_39766 Human_SNP_ID_626689787 A-to-I Human chr17 + 50730057 50730057 50730057 CTCACTGCAGCTTCCACCTCCTGGGCTCTAGCAGTCCTCCCACTGCTTGAGCAGGCTCCTCCCAT CTCACTGCAGCTTCCACCTCCTGGGCTCTAGCGGTCCTCCCACTGCTTGAGCAGGCTCCTCCCAT A G LUC7L3 Ensembl:ENSG00000108848 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs566998156 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1287378,Human_RBP_ID_17566007 39767 RMVar_ID_39767 Human_SNP_ID_626689810 A-to-I Human chr17 + 50730115 50730115 50730115 CTCCCATTCCAGCCTCCTGAGTAGCTGGGACTATAGGCCCGCACCACCCCTGGCTAATTTTTTTG CTCCCATTCCAGCCTCCTGAGTAGCTGGGACTGTAGGCCCGCACCACCCCTGGCTAATTTTTTTG A G LUC7L3 Ensembl:ENSG00000108848 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1391090526 Functional Loss SNV dbSNP153 33..33 33 - - - 39768 RMVar_ID_39768 Human_SNP_ID_626689820 A-to-I Human chr17 + 50730138 50730138 50730138 GCTGGGACTATAGGCCCGCACCACCCCTGGCTAATTTTTTTGTATTGGTGGAGATGGGGTCTTGC GCTGGGACTATAGGCCCGCACCACCCCTGGCTGATTTTTTTGTATTGGTGGAGATGGGGTCTTGC A G LUC7L3 Ensembl:ENSG00000108848 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs994324550 Functional Loss SNV dbSNP153 33..33 33 - - - 39769 RMVar_ID_39769 Human_SNP_ID_626689892 A-to-I Human chr17 + 50730400 50730400 50730400 AAAATTAGCCAGGCATGGTGGCAGTTGCCCATAATCCCAGCTTGGGAGGCTGAGGCACGAGAATT AAAATTAGCCAGGCATGGTGGCAGTTGCCCATGATCCCAGCTTGGGAGGCTGAGGCACGAGAATT A G LUC7L3 Ensembl:ENSG00000108848 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs372132701 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17566010 39770 RMVar_ID_39770 Human_SNP_ID_626689903 A-to-I Human chr17 + 50730450 50730450 50730450 TGAGGCACGAGAATTGCTTGAGCCTGGGAGGTAGAGGTAGTGAGCCAAGATCGAACCACTGCACT TGAGGCACGAGAATTGCTTGAGCCTGGGAGGTGGAGGTAGTGAGCCAAGATCGAACCACTGCACT A G LUC7L3 Ensembl:ENSG00000108848 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs961049662 Functional Loss SNV dbSNP153 33..33 33 - - - 39771 RMVar_ID_39771 Human_SNP_ID_626689906 A-to-I Human chr17 + 50730460 50730460 50730460 GAATTGCTTGAGCCTGGGAGGTAGAGGTAGTGAGCCAAGATCGAACCACTGCACTCCAGCCTGGG GAATTGCTTGAGCCTGGGAGGTAGAGGTAGTGGGCCAAGATCGAACCACTGCACTCCAGCCTGGG A G LUC7L3 Ensembl:ENSG00000108848 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1364561915 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25299243 39772 RMVar_ID_39772 Human_SNP_ID_626690636 A-to-I Human chr17 + 50732776 50732776 50732776 TTTTTTCTTTTTTAGACAGGTTGCGTTCTGTCACCCTAGCTGGAGTGCAGCGGTGTGATCACAGC TTTTTTCTTTTTTAGACAGGTTGCGTTCTGTCCCCCTAGCTGGAGTGCAGCGGTGTGATCACAGC A C LUC7L3 Ensembl:ENSG00000108848 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7215460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13219899 39773 RMVar_ID_39773 Human_SNP_ID_626690637 A-to-I Human chr17 + 50732776 50732776 50732776 TTTTTTCTTTTTTAGACAGGTTGCGTTCTGTCACCCTAGCTGGAGTGCAGCGGTGTGATCACAGC TTTTTTCTTTTTTAGACAGGTTGCGTTCTGTCGCCCTAGCTGGAGTGCAGCGGTGTGATCACAGC A G LUC7L3 Ensembl:ENSG00000108848 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7215460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13219899 39774 RMVar_ID_39774 Human_SNP_ID_626690638 A-to-I Human chr17 + 50732776 50732776 50732776 TTTTTTCTTTTTTAGACAGGTTGCGTTCTGTCACCCTAGCTGGAGTGCAGCGGTGTGATCACAGC TTTTTTCTTTTTTAGACAGGTTGCGTTCTGTCTCCCTAGCTGGAGTGCAGCGGTGTGATCACAGC A T LUC7L3 Ensembl:ENSG00000108848 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7215460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13219899 39775 RMVar_ID_39775 Human_SNP_ID_626691556 A-to-I Human chr17 + 50735605 50735605 50735605 ATGGCTCATTGCAGCCTCGACCTCCCAGGCTCAAGCAATCCTTCTGCCTCAGCCTCCTGGGTAGC ATGGCTCATTGCAGCCTCGACCTCCCAGGCTCGAGCAATCCTTCTGCCTCAGCCTCCTGGGTAGC A G LUC7L3 Ensembl:ENSG00000108848 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs765520648 Functional Loss SNV dbSNP153 33..33 33 - - - 39776 RMVar_ID_39776 Human_SNP_ID_626691577 A-to-I Human chr17 + 50735679 50735679 50735679 GCCACCATGCCTGGCTACTTTCTGTATTTTTTATAGACATGGGGTTTTGCCATGTTGCCCAAGCC GCCACCATGCCTGGCTACTTTCTGTATTTTTTGTAGACATGGGGTTTTGCCATGTTGCCCAAGCC A G LUC7L3 Ensembl:ENSG00000108848 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs371553361 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25299308 39777 RMVar_ID_39777 Human_SNP_ID_626691641 A-to-I Human chr17 + 50735937 50735937 50735937 GGCAAATCACTTGAGGTCAGGAGTTCGAGACCAGCCTGACCAACATGGTGAAACCCTGTCTGTAC GGCAAATCACTTGAGGTCAGGAGTTCGAGACCGGCCTGACCAACATGGTGAAACCCTGTCTGTAC A G LUC7L3 Ensembl:ENSG00000108848 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1390345364 Functional Loss SNV dbSNP153 33..33 33 - - - 39778 RMVar_ID_39778 Human_SNP_ID_626691649 A-to-I Human chr17 + 50735974 50735974 50735974 GACCAACATGGTGAAACCCTGTCTGTACTAAAAATACAAAAACTAGCTGGGCATGGTGGCACATA GACCAACATGGTGAAACCCTGTCTGTACTAAAGATACAAAAACTAGCTGGGCATGGTGGCACATA A G LUC7L3 Ensembl:ENSG00000108848 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs904310232 Functional Loss SNV dbSNP153 33..33 33 - - - 39779 RMVar_ID_39779 Human_SNP_ID_626691668 A-to-I Human chr17 + 50736053 50736053 50736053 TACTTTGGAGACTGAGGCAGAACAATTGCTTGAACCTGGGAGGCGGAGCTTGCAGTGGGCTGAGA TACTTTGGAGACTGAGGCAGAACAATTGCTTGTACCTGGGAGGCGGAGCTTGCAGTGGGCTGAGA A T LUC7L3 Ensembl:ENSG00000108848 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1268486535 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17565607,Human_RBP_ID_25299318 39780 RMVar_ID_39780 Human_SNP_ID_626693307 A-to-I Human chr17 + 50741933 50741933 50741933 AAAGTGAGACCCAGTCTTTACAAAAATTAGCCAGGTGCAATGGCGTGTACCTGTGGTCCCAGCTA AAAGTGAGACCCAGTCTTTACAAAAATTAGCCGGGTGCAATGGCGTGTACCTGTGGTCCCAGCTA A G LUC7L3 Ensembl:ENSG00000108848 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs9900774 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9867237,Human_RBP_ID_17895811 RMVar_hsa_circ_321545,RMVar_hsa_circ_355377,RMVar_hsa_circ_367342,RMVar_hsa_circ_17259,RMVar_hsa_circ_185377,RMVar_hsa_circ_351997,RMVar_hsa_circ_119164,RMVar_hsa_circ_185379 39781 RMVar_ID_39781 Human_SNP_ID_626693489 A-to-I Human chr17 + 50742488 50742488 50742488 TCAAATGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGTGTGCGCCACCATCCCCG TCAAATGATTCTCCTGCCTCAGCCTCCCGAGTGGCTGGGATTACAGGTGTGCGCCACCATCCCCG A G LUC7L3 Ensembl:ENSG00000108848 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256758285 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23734446 RMVar_hsa_circ_321545,RMVar_hsa_circ_355377,RMVar_hsa_circ_367342,RMVar_hsa_circ_17259,RMVar_hsa_circ_185377,RMVar_hsa_circ_351997,RMVar_hsa_circ_119164,RMVar_hsa_circ_185379 39782 RMVar_ID_39782 Human_SNP_ID_626697679 A-to-I Human chr17 - 50757593 50757593 50757593 GTAGAGACAGGGTTTCACTATGTTGGCCAGGCAGGTCTTGAACTCCTGACCTCATGATCCGACTG GTAGAGACAGGGTTTCACTATGTTGGCCAGGCTGGTCTTGAACTCCTGACCTCATGATCCGACTG T A lnc-LINC00483-1,lnc-LINC00483-1:2,lnc-LINC00483-1:3,lnc-LINC00483-1:4 RNACentral:URS0000D5C510,RNACentral:URS0000D5D367,RNACentral:URS00008BDAD9,RNACentral:URS0000D5E17C lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1420710968 Functional Loss SNV dbSNP153 33..33 33 - - - 39783 RMVar_ID_39783 Human_SNP_ID_626697681 A-to-I Human chr17 - 50757606 50757604 50757606 TTTTTTTTTTTTAGTAGAGACAGGGTTTCACTATGTTGGCCAGGCAGGTCTTGAACTCCTGACCT TTTTTTTTTTTTAGTAGAGACAGGGTTTCACT__GTTGGCCAGGCAGGTCTTGAACTCCTGACCT CAT C lnc-LINC00483-1,lnc-LINC00483-1:2,lnc-LINC00483-1:3,lnc-LINC00483-1:4 RNACentral:URS0000D5C510,RNACentral:URS0000D5D367,RNACentral:URS00008BDAD9,RNACentral:URS0000D5E17C lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1390485642 Functional Loss DEL dbSNP153 33..34 33 - - - 39784 RMVar_ID_39784 Human_SNP_ID_626698798 A-to-I Human chr17 - 50761210 50761209 50761210 GAAACCCAGTCTCTACTAAAAAAAATACAAAAATTAGCTAGGTGTGGTGGCGCACACCTGTAGTA GAAACCCAGTCTCTACTAAAAAAAATACAAAA_TTAGCTAGGTGTGGTGGCGCACACCTGTAGTA AT A ANKRD40CL Ensembl:ENSG00000167117 Protein coding exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1362005825 Functional Loss DEL dbSNP153 33..33 33 - - - 39785 RMVar_ID_39785 Human_SNP_ID_626698802 A-to-I Human chr17 - 50761219 50761219 50761219 ACATATAGTGAAACCCAGTCTCTACTAAAAAAAATACAAAAATTAGCTAGGTGTGGTGGCGCACA ACATATAGTGAAACCCAGTCTCTACTAAAAAATATACAAAAATTAGCTAGGTGTGGTGGCGCACA T A ANKRD40CL Ensembl:ENSG00000167117 Protein coding exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1390699767 Functional Loss SNV dbSNP153 33..33 33 - - - 39786 RMVar_ID_39786 Human_SNP_ID_626731754 A-to-I Human chr17 - 50888794 50888794 50888794 TGATCTATCCACCTTGGCTTCCCAAAAATACTAGGATTACAGGCATGAGCCACTCACTGCTCCCG TGATCTATCCACCTTGGCTTCCCAAAAATACTGGGATTACAGGCATGAGCCACTCACTGCTCCCG T C HSALNG0117346 RNACentral:URS0000E9915F lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs781406986 Functional Loss SNV dbSNP153 33..33 33 - - - 39787 RMVar_ID_39787 Human_SNP_ID_626750379 A-to-I Human chr17 - 50964331 50964331 50964331 TACCCGCCTTGGCCTCCCGAAGTGCTTGAATTACAGGCGTGAGCCCCCGCGCCGGTCCGAAGCAA TACCCGCCTTGGCCTCCCGAAGTGCTTGAATTGCAGGCGTGAGCCCCCGCGCCGGTCCGAAGCAA T C SPAG9 Ensembl:ENSG00000008294 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1055361 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26453193 Human_Splice_Rec_1841928 Human_miRNA_ID_2250322 RMVar_hsa_circ_103413,RMVar_hsa_circ_119329,RMVar_hsa_circ_185389,RMVar_hsa_circ_95841,RMVar_hsa_circ_185390,RMVar_hsa_circ_185388 39788 RMVar_ID_39788 Human_SNP_ID_626750393 A-to-I Human chr17 - 50964385 50964385 50964385 CAGGGTTTCACCACATTGGCCAGGCTGGTCTCAAACTCCTGACCTCAGATGATCTACCCGCCTTG CAGGGTTTCACCACATTGGCCAGGCTGGTCTCTAACTCCTGACCTCAGATGATCTACCCGCCTTG T A SPAG9 Ensembl:ENSG00000008294 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,31158229,32596459 RNA-Seq:(High) rs1466189671 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1841928 Human_miRNA_ID_891503,Human_miRNA_ID_2404452 RMVar_hsa_circ_103413,RMVar_hsa_circ_119329,RMVar_hsa_circ_185389,RMVar_hsa_circ_95841,RMVar_hsa_circ_185390,RMVar_hsa_circ_185388 39789 RMVar_ID_39789 Human_SNP_ID_626750396 A-to-I Human chr17 - 50964403 50964403 50964403 TTGTATTTTTAGTAGAGACAGGGTTTCACCACATTGGCCAGGCTGGTCTCAAACTCCTGACCTCA TTGTATTTTTAGTAGAGACAGGGTTTCACCACGTTGGCCAGGCTGGTCTCAAACTCCTGACCTCA T C SPAG9 Ensembl:ENSG00000008294 Protein coding 3'UTR GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 29796672,31158229,31158229 RNA-Seq:(High) rs1404387082 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4438493 Human_miRNA_ID_733224 RMVar_hsa_circ_103413,RMVar_hsa_circ_119329,RMVar_hsa_circ_185389,RMVar_hsa_circ_95841,RMVar_hsa_circ_185390,RMVar_hsa_circ_185388 39790 RMVar_ID_39790 Human_SNP_ID_626750409 A-to-I Human chr17 - 50964505 50964505 50964505 CAGCTCACTGCAACCTCCACCTCTCAGGTTCAAGTAGTTCTCCTGCCTCAGCCTCCCAAGTAGCT CAGCTCACTGCAACCTCCACCTCTCAGGTTCATGTAGTTCTCCTGCCTCAGCCTCCCAAGTAGCT T A SPAG9 Ensembl:ENSG00000008294 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229 RNA-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 39791 RMVar_ID_39791 Human_SNP_ID_626750421 A-to-I Human chr17 - 50964536 50964536 50964536 TTGCCCAGGCTGGAATGCAGTGGTGCGATCTCAGCTCACTGCAACCTCCACCTCTCAGGTTCAAG TTGCCCAGGCTGGAATGCAGTGGTGCGATCTCTGCTCACTGCAACCTCCACCTCTCAGGTTCAAG T A SPAG9 Ensembl:ENSG00000008294 Protein coding 3'UTR GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1290190331 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 39792 RMVar_ID_39792 Human_SNP_ID_626750515 A-to-I Human chr17 - 50964818 50964818 50964818 GGCCCAGGAGGTGGAGGTTGCAGTGAGCCTTGATAGCACCACTGCACTCCAGCCTGGGTGACGGA GGCCCAGGAGGTGGAGGTTGCAGTGAGCCTTGGTAGCACCACTGCACTCCAGCCTGGGTGACGGA T C SPAG9 Ensembl:ENSG00000008294 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1249612712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13069218,Human_RBP_ID_23170525,Human_RBP_ID_26453196 Human_miRNA_ID_760346,Human_miRNA_ID_1324839 RMVar_hsa_circ_103413,RMVar_hsa_circ_119329,RMVar_hsa_circ_185389,RMVar_hsa_circ_95841,RMVar_hsa_circ_185390,RMVar_hsa_circ_185388 39793 RMVar_ID_39793 Human_SNP_ID_626750524 A-to-I Human chr17 - 50964845 50964845 50964845 GGGAGGCTGAGGTGGGAGGATGACCTGGGCCCAGGAGGTGGAGGTTGCAGTGAGCCTTGATAGCA GGGAGGCTGAGGTGGGAGGATGACCTGGGCCCGGGAGGTGGAGGTTGCAGTGAGCCTTGATAGCA T C SPAG9 Ensembl:ENSG00000008294 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs750194914 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6612449,Human_RBP_ID_13069219,Human_RBP_ID_26457983 RMVar_hsa_circ_103413,RMVar_hsa_circ_119329,RMVar_hsa_circ_185389,RMVar_hsa_circ_95841,RMVar_hsa_circ_185390,RMVar_hsa_circ_185388 39794 RMVar_ID_39794 Human_SNP_ID_626750575 A-to-I Human chr17 - 50965007 50965007 50965007 CCTGTAATCCCAACACTTTAGGAGGCTGAGGCAGATGGATTGCTTGAGCCCAGGAGTTCAAGACC CCTGTAATCCCAACACTTTAGGAGGCTGAGGCGGATGGATTGCTTGAGCCCAGGAGTTCAAGACC T C SPAG9 Ensembl:ENSG00000008294 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1460053780 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26453197 RMVar_hsa_circ_103413,RMVar_hsa_circ_119329,RMVar_hsa_circ_185389,RMVar_hsa_circ_95841,RMVar_hsa_circ_185390,RMVar_hsa_circ_185388 39795 RMVar_ID_39795 Human_SNP_ID_626750579 A-to-I Human chr17 - 50965027 50965027 50965027 GTTGGGCATGGTGGCTCACGCCTGTAATCCCAACACTTTAGGAGGCTGAGGCAGATGGATTGCTT GTTGGGCATGGTGGCTCACGCCTGTAATCCCAGCACTTTAGGAGGCTGAGGCAGATGGATTGCTT T C SPAG9 Ensembl:ENSG00000008294 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1133791 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4438516,Human_RBP_ID_26453197 RMVar_hsa_circ_103413,RMVar_hsa_circ_119329,RMVar_hsa_circ_185389,RMVar_hsa_circ_95841,RMVar_hsa_circ_185390,RMVar_hsa_circ_185388 39796 RMVar_ID_39796 Human_SNP_ID_626750589 A-to-I Human chr17 - 50965061 50965061 50965061 TTCATTCACAATGCCCATTAAAAAAAAAAAATAGGTTGGGCATGGTGGCTCACGCCTGTAATCCC TTCATTCACAATGCCCATTAAAAAAAAAAAATGGGTTGGGCATGGTGGCTCACGCCTGTAATCCC T C SPAG9 Ensembl:ENSG00000008294 Protein coding 3'UTR GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 29129909,30559470 RNA-Seq:(High) rs995062057 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13069220,Human_RBP_ID_23170527,Human_RBP_ID_26453198 Human_Splice_Rec_1841927 RMVar_hsa_circ_103413,RMVar_hsa_circ_119329,RMVar_hsa_circ_185389,RMVar_hsa_circ_95841,RMVar_hsa_circ_185390,RMVar_hsa_circ_185388 39797 RMVar_ID_39797 Human_SNP_ID_626764752 A-to-I Human chr17 - 51023789 51023787 51023789 ATGGTGACGCACGCCGGTAATCATAGGTGCTCAGGGGACTGAGGCACGAGAATCGCTTGAGCCTG ATGGTGACGCACGCCGGTAATCATAGGTGCTC__GGGACTGAGGCACGAGAATCGCTTGAGCCTG CCT C SPAG9 Ensembl:ENSG00000008294 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947316116 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_13070014,Human_RBP_ID_25300204 RMVar_hsa_circ_2266,RMVar_hsa_circ_67403,RMVar_hsa_circ_27905,RMVar_hsa_circ_98563,RMVar_hsa_circ_376990,RMVar_hsa_circ_8056,RMVar_hsa_circ_5212,RMVar_hsa_circ_185426,RMVar_hsa_circ_325252,RMVar_hsa_circ_335208,RMVar_hsa_circ_337731,RMVar_hsa_circ_185432,RMVar_hsa_circ_324741,RMVar_hsa_circ_185428,RMVar_hsa_circ_369943,RMVar_hsa_circ_340857,RMVar_hsa_circ_307715,RMVar_hsa_circ_282424,RMVar_hsa_circ_185430,RMVar_hsa_circ_185431,RMVar_hsa_circ_372222,RMVar_hsa_circ_185433 39798 RMVar_ID_39798 Human_SNP_ID_626764753 A-to-I Human chr17 - 51023789 51023789 51023789 ATGGTGACGCACGCCGGTAATCATAGGTGCTCAGGGGACTGAGGCACGAGAATCGCTTGAGCCTG ATGGTGACGCACGCCGGTAATCATAGGTGCTCGGGGGACTGAGGCACGAGAATCGCTTGAGCCTG T C SPAG9 Ensembl:ENSG00000008294 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1568011524 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13070014,Human_RBP_ID_25300204 RMVar_hsa_circ_2266,RMVar_hsa_circ_67403,RMVar_hsa_circ_27905,RMVar_hsa_circ_98563,RMVar_hsa_circ_376990,RMVar_hsa_circ_8056,RMVar_hsa_circ_5212,RMVar_hsa_circ_185426,RMVar_hsa_circ_325252,RMVar_hsa_circ_335208,RMVar_hsa_circ_337731,RMVar_hsa_circ_185432,RMVar_hsa_circ_324741,RMVar_hsa_circ_185428,RMVar_hsa_circ_369943,RMVar_hsa_circ_340857,RMVar_hsa_circ_307715,RMVar_hsa_circ_282424,RMVar_hsa_circ_185430,RMVar_hsa_circ_185431,RMVar_hsa_circ_372222,RMVar_hsa_circ_185433 39799 RMVar_ID_39799 Human_SNP_ID_626766994 A-to-I Human chr17 - 51032895 51032895 51032895 AGTTTCGCTCTTGTTGCCCAGGATGTAGTGCAATGGCGTGATCTCGGCTCACTGCAACCTCCTCC AGTTTCGCTCTTGTTGCCCAGGATGTAGTGCAGTGGCGTGATCTCGGCTCACTGCAACCTCCTCC T C SPAG9 Ensembl:ENSG00000008294 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042482793 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67403,RMVar_hsa_circ_27905,RMVar_hsa_circ_98563,RMVar_hsa_circ_376990,RMVar_hsa_circ_5212,RMVar_hsa_circ_185426,RMVar_hsa_circ_335208,RMVar_hsa_circ_337731,RMVar_hsa_circ_185432,RMVar_hsa_circ_324741,RMVar_hsa_circ_185428,RMVar_hsa_circ_369943,RMVar_hsa_circ_340857,RMVar_hsa_circ_307715,RMVar_hsa_circ_185431,RMVar_hsa_circ_372222,RMVar_hsa_circ_16537,RMVar_hsa_circ_185433,RMVar_hsa_circ_312304 39800 RMVar_ID_39800 Human_SNP_ID_626777352 A-to-I Human chr17 - 51075748 51075748 51075748 ACGATCATAGCTCACTGTATCCTTGAACTCCCAGGCTCAAGTGATCCTCCCACCTTAGCCTCCCA ACGATCATAGCTCACTGTATCCTTGAACTCCCGGGCTCAAGTGATCCTCCCACCTTAGCCTCCCA T C SPAG9 Ensembl:ENSG00000008294 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971286862 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8456820,Human_RBP_ID_13070696 RMVar_hsa_circ_67403,RMVar_hsa_circ_335208,RMVar_hsa_circ_324741,RMVar_hsa_circ_185434,RMVar_hsa_circ_290244,RMVar_hsa_circ_185438,RMVar_hsa_circ_272391,RMVar_hsa_circ_323882 39801 RMVar_ID_39801 Human_SNP_ID_626780394 A-to-I Human chr17 - 51086759 51086759 51086759 TGCCACCACGCCCAGCTAACTTTTGTGTTTTTAGTAGAGACTGAGTTTCACCATCTTGGCTAGGC TGCCACCACGCCCAGCTAACTTTTGTGTTTTTGGTAGAGACTGAGTTTCACCATCTTGGCTAGGC T C SPAG9 Ensembl:ENSG00000008294 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935986256 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17005319 39802 RMVar_ID_39802 Human_SNP_ID_626788357 A-to-I Human chr17 - 51115327 51115327 51115327 AAAATTAGTTGGGTGTGATGGTGTGAGCCTGTAGTCCTAGCTACTCAGGAGGCTAAGGCAGGAGG AAAATTAGTTGGGTGTGATGGTGTGAGCCTGTTGTCCTAGCTACTCAGGAGGCTAAGGCAGGAGG T A SPAG9 Ensembl:ENSG00000008294 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232608810 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25300604 39803 RMVar_ID_39803 Human_SNP_ID_626800793 A-to-I Human chr17 + 51163089 51163089 51163089 TGAGACCTCATCTCTGCCAAACATTAAAAATTAGTCGGGTGTGGTGGCACATTCCTGTAGTCCTA TGAGACCTCATCTCTGCCAAACATTAAAAATTTGTCGGGTGTGGTGGCACATTCCTGTAGTCCTA A T NME1-NME2 Ensembl:ENSG00000011052 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1212381951 Functional Loss SNV dbSNP153 33..33 33 - - - 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_185445 39804 RMVar_ID_39804 Human_SNP_ID_626800828 A-to-I Human chr17 + 51163279 51163279 51163279 CCTAGCTGCTCAGTAGGGGTGGTGATAGTGGTAAGGCTCTGATCTTTAAGGTGGTCTACACACAC CCTAGCTGCTCAGTAGGGGTGGTGATAGTGGTGAGGCTCTGATCTTTAAGGTGGTCTACACACAC A G NME1-NME2 Ensembl:ENSG00000011052 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1231780230 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1182927,Human_RBP_ID_13071892 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_185445 39805 RMVar_ID_39805 Human_SNP_ID_626800935 A-to-I Human chr17 + 51163773 51163773 51163773 TGCCTGCCTGGGCCTCCCAAAGTGCTGAGATTATAGGCGTGAGCCACTGCGCCCACCCTGAGGGT TGCCTGCCTGGGCCTCCCAAAGTGCTGAGATTGTAGGCGTGAGCCACTGCGCCCACCCTGAGGGT A G NME1-NME2 Ensembl:ENSG00000011052 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1370020198 Functional Loss SNV dbSNP153 33..33 33 - - - 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_185445 39806 RMVar_ID_39806 Human_SNP_ID_626801000 A-to-I Human chr17 + 51163959 51163959 51163959 CCTGTCTCAGCCTCCTGAGTAGCTGGGATTACAGGTGTGTGCCACCACTCCCGGCTATTTTTTGT CCTGTCTCAGCCTCCTGAGTAGCTGGGATTACCGGTGTGTGCCACCACTCCCGGCTATTTTTTGT A C NME1-NME2 Ensembl:ENSG00000011052 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs562690133 Functional Loss SNV dbSNP153 33..33 33 - - - 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_185445 39807 RMVar_ID_39807 Human_SNP_ID_626802783 A-to-I Human chr17 + 51170325 51170325 51170325 TGCCACGCCCGGCTAATTTTTGTATTTTTAGTAGAGATGGTTTCACCACGTTGGCCAGGCTAGTT TGCCACGCCCGGCTAATTTTTGTATTTTTAGTCGAGATGGTTTCACCACGTTGGCCAGGCTAGTT A C NME2,NME1-NME2 Ensembl:ENSG00000243678,Ensembl:ENSG00000011052 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1239309956 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 39808 RMVar_ID_39808 Human_SNP_ID_626802865 A-to-I Human chr17 + 51170648 51170648 51170648 CCCCGTCTCTACTAAAAGTAAAAAATTAGGGCATGGTGGTGCATGCCTGTAATCCTAGCTACTCA CCCCGTCTCTACTAAAAGTAAAAAATTAGGGCGTGGTGGTGCATGCCTGTAATCCTAGCTACTCA A G NME2,NME1-NME2 Ensembl:ENSG00000243678,Ensembl:ENSG00000011052 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1399910603 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 39809 RMVar_ID_39809 Human_SNP_ID_626802868 A-to-I Human chr17 + 51170680 51170680 51170680 ATGGTGGTGCATGCCTGTAATCCTAGCTACTCAGGAGGCTGAGACAGAAGAATCGCTTGAACCTG ATGGTGGTGCATGCCTGTAATCCTAGCTACTCGGGAGGCTGAGACAGAAGAATCGCTTGAACCTG A G NME2,NME1-NME2 Ensembl:ENSG00000243678,Ensembl:ENSG00000011052 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1252750418 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 39810 RMVar_ID_39810 Human_SNP_ID_626808504 A-to-I Human chr17 - 51190962 51190962 51190962 CTCCCACCCCAGCCTCCTGAGTAGCTTGGACCACAGGCATGTGTTGCCACACACCCAGCTAAGTT CTCCCACCCCAGCCTCCTGAGTAGCTTGGACCGCAGGCATGTGTTGCCACACACCCAGCTAAGTT T C MBTD1 Ensembl:ENSG00000011258 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1261474004 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13072578 39811 RMVar_ID_39811 Human_SNP_ID_626809225 A-to-I Human chr17 - 51193867 51193864 51193868 CCAATAATCCCAGCACTTTGGGAGACTCAGGTAGGAGGATTGCTTGAGACCAGGAGTTTGAGAAC CCAATAATCCCAGCACTTTGGGAGACTCAGG____AGGATTGCTTGAGACCAGGAGTTTGAGAAC TCCTA T MBTD1 Ensembl:ENSG00000011258 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1328359991 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_17566028 RMVar_hsa_circ_4143,RMVar_hsa_circ_337618,RMVar_hsa_circ_346320,RMVar_hsa_circ_46287,RMVar_hsa_circ_32232,RMVar_hsa_circ_72450,RMVar_hsa_circ_269325 39812 RMVar_ID_39812 Human_SNP_ID_626809504 A-to-I Human chr17 - 51194827 51194827 51194827 GGAGTGCAGTGGCACAATCATAGCTCACGGTAACTTCAACTCCTGGGCCCAAGGAATCCTCCCAC GGAGTGCAGTGGCACAATCATAGCTCACGGTACCTTCAACTCCTGGGCCCAAGGAATCCTCCCAC T G MBTD1 Ensembl:ENSG00000011258 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1227058658 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4143,RMVar_hsa_circ_337618,RMVar_hsa_circ_346320,RMVar_hsa_circ_46287,RMVar_hsa_circ_32232,RMVar_hsa_circ_72450,RMVar_hsa_circ_269325 39813 RMVar_ID_39813 Human_SNP_ID_626810046 A-to-I Human chr17 - 51196853 51196853 51196853 CAGTCTTGCTCTGTCACCCAGGCTGGAGTGCAATGGCATGGTCTCGGCTCACTGCAGCCTCTGCC CAGTCTTGCTCTGTCACCCAGGCTGGAGTGCAGTGGCATGGTCTCGGCTCACTGCAGCCTCTGCC T C MBTD1 Ensembl:ENSG00000011258 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs994895757 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4143,RMVar_hsa_circ_337618,RMVar_hsa_circ_346320,RMVar_hsa_circ_46287,RMVar_hsa_circ_185453,RMVar_hsa_circ_32232,RMVar_hsa_circ_72450,RMVar_hsa_circ_269325,RMVar_hsa_circ_280037,RMVar_hsa_circ_316526,RMVar_hsa_circ_185454 39814 RMVar_ID_39814 Human_SNP_ID_626810338 A-to-I Human chr17 - 51197623 51197623 51197623 GCACACCTATAGACCCAGCTATCCAGGAGGCTAGGGTGGGAGCATCACCTGAGCTCAGGGAAGTT GCACACCTATAGACCCAGCTATCCAGGAGGCTGGGGTGGGAGCATCACCTGAGCTCAGGGAAGTT T C MBTD1 Ensembl:ENSG00000011258 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985188134 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_819785,Human_RBP_ID_21890808 RMVar_hsa_circ_4143,RMVar_hsa_circ_337618,RMVar_hsa_circ_346320,RMVar_hsa_circ_46287,RMVar_hsa_circ_185453,RMVar_hsa_circ_32232,RMVar_hsa_circ_72450,RMVar_hsa_circ_269325,RMVar_hsa_circ_280037,RMVar_hsa_circ_316526,RMVar_hsa_circ_185454 39815 RMVar_ID_39815 Human_SNP_ID_626810339 A-to-I Human chr17 - 51197623 51197623 51197623 GCACACCTATAGACCCAGCTATCCAGGAGGCTAGGGTGGGAGCATCACCTGAGCTCAGGGAAGTT GCACACCTATAGACCCAGCTATCCAGGAGGCTCGGGTGGGAGCATCACCTGAGCTCAGGGAAGTT T G MBTD1 Ensembl:ENSG00000011258 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985188134 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_819785,Human_RBP_ID_21890808 RMVar_hsa_circ_4143,RMVar_hsa_circ_337618,RMVar_hsa_circ_346320,RMVar_hsa_circ_46287,RMVar_hsa_circ_185453,RMVar_hsa_circ_32232,RMVar_hsa_circ_72450,RMVar_hsa_circ_269325,RMVar_hsa_circ_280037,RMVar_hsa_circ_316526,RMVar_hsa_circ_185454 39816 RMVar_ID_39816 Human_SNP_ID_626811185 A-to-I Human chr17 - 51200910 51200910 51200910 TTCCTGGGCTCAGGCAATCCTCCTAAAGTGCTAGGATTATAGGCATGAGCCACGGCACCCAGCAT TTCCTGGGCTCAGGCAATCCTCCTAAAGTGCTGGGATTATAGGCATGAGCCACGGCACCCAGCAT T C MBTD1 Ensembl:ENSG00000011258 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs957226618 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4143,RMVar_hsa_circ_337618,RMVar_hsa_circ_346320,RMVar_hsa_circ_46287,RMVar_hsa_circ_185453,RMVar_hsa_circ_32232,RMVar_hsa_circ_72450,RMVar_hsa_circ_269325,RMVar_hsa_circ_280037,RMVar_hsa_circ_316526,RMVar_hsa_circ_185454 39817 RMVar_ID_39817 Human_SNP_ID_626816756 A-to-I Human chr17 - 51223348 51223348 51223348 TATTTTTTTCAGAGACGGGCAATTTTCACCATATTGCCCAGGCTGGTCTCAAACTCCTGAACTCA TATTTTTTTCAGAGACGGGCAATTTTCACCATGTTGCCCAGGCTGGTCTCAAACTCCTGAACTCA T C MBTD1 Ensembl:ENSG00000011258 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs979924105 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_337618,RMVar_hsa_circ_6785,RMVar_hsa_circ_297460,RMVar_hsa_circ_185458,RMVar_hsa_circ_185461,RMVar_hsa_circ_105181,RMVar_hsa_circ_297091,RMVar_hsa_circ_10706,RMVar_hsa_circ_185463,RMVar_hsa_circ_326489,RMVar_hsa_circ_185471,RMVar_hsa_circ_276868,RMVar_hsa_circ_326675,RMVar_hsa_circ_77547,RMVar_hsa_circ_185469,RMVar_hsa_circ_185470,RMVar_hsa_circ_292708,RMVar_hsa_circ_185472 39818 RMVar_ID_39818 Human_SNP_ID_626816907 A-to-I Human chr17 - 51223822 51223822 51223822 GAAATTGTTGTTGTTGTTGTTGAGACAGTCTCACTCTGATGCCCAAGCTGGAGTGCAGTGGTGCA GAAATTGTTGTTGTTGTTGTTGAGACAGTCTCTCTCTGATGCCCAAGCTGGAGTGCAGTGGTGCA T A MBTD1 Ensembl:ENSG00000011258 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs377530454 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21927568 RMVar_hsa_circ_337618,RMVar_hsa_circ_6785,RMVar_hsa_circ_297460,RMVar_hsa_circ_185458,RMVar_hsa_circ_185461,RMVar_hsa_circ_105181,RMVar_hsa_circ_297091,RMVar_hsa_circ_10706,RMVar_hsa_circ_185463,RMVar_hsa_circ_326489,RMVar_hsa_circ_185471,RMVar_hsa_circ_276868,RMVar_hsa_circ_326675,RMVar_hsa_circ_77547,RMVar_hsa_circ_185469,RMVar_hsa_circ_185470,RMVar_hsa_circ_292708,RMVar_hsa_circ_185472 39819 RMVar_ID_39819 Human_SNP_ID_626820243 A-to-I Human chr17 - 51236370 51236370 51236370 ATAGTGGCACACACCTGTAATCCTAGCCACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACCCA ATAGTGGCACACACCTGTAATCCTAGCCACTCTGGAGGCTGAGGCAGGAGAATCGCTTGAACCCA T A MBTD1 Ensembl:ENSG00000011258 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs936832154 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6785,RMVar_hsa_circ_185471,RMVar_hsa_circ_326675,RMVar_hsa_circ_77547 39820 RMVar_ID_39820 Human_SNP_ID_626820914 A-to-I Human chr17 - 51238943 51238943 51238943 GACGCACATTACCACACCCAGTTAATTTTTGTATTTTTAGTAGAGACAGGGTTTTACCATGTTAG GACGCACATTACCACACCCAGTTAATTTTTGTGTTTTTAGTAGAGACAGGGTTTTACCATGTTAG T C MBTD1 Ensembl:ENSG00000011258 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs887235160 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6785,RMVar_hsa_circ_185471,RMVar_hsa_circ_326675,RMVar_hsa_circ_77547 39821 RMVar_ID_39821 Human_SNP_ID_626821486 A-to-I Human chr17 - 51241070 51241070 51241070 GGAGGCCGAAGCAAAAGGATTGCTTGAACCCTAGAGGTGGAGGTTGCAGTGAGCCGAAATCACGC GGAGGCCGAAGCAAAAGGATTGCTTGAACCCTGGAGGTGGAGGTTGCAGTGAGCCGAAATCACGC T C MBTD1 Ensembl:ENSG00000011258 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1248903536 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25301081 RMVar_hsa_circ_6785,RMVar_hsa_circ_185471,RMVar_hsa_circ_326675,RMVar_hsa_circ_77547 39822 RMVar_ID_39822 Human_SNP_ID_626824590 A-to-I Human chr17 - 51252651 51252651 51252651 TGGCTCTCTGCAACCTTCGCCTCCCGGGTTCAAGTGATTCTTCTGCCTCAGCCTCCCTGGTAGCT TGGCTCTCTGCAACCTTCGCCTCCCGGGTTCAGGTGATTCTTCTGCCTCAGCCTCCCTGGTAGCT T C MBTD1 Ensembl:ENSG00000011258 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1038494543 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17566031 RMVar_hsa_circ_6785,RMVar_hsa_circ_185471,RMVar_hsa_circ_326675,RMVar_hsa_circ_77547 39823 RMVar_ID_39823 Human_SNP_ID_626825193 A-to-I Human chr17 - 51255181 51255181 51255181 CGCCTCCCGGGTTCAAGTGATTCTTCTGCCTCAGCCTCCCGAGTGGCTGGGACTACAGGCAAATG CGCCTCCCGGGTTCAAGTGATTCTTCTGCCTCTGCCTCCCGAGTGGCTGGGACTACAGGCAAATG T A MBTD1 Ensembl:ENSG00000011258 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1461079777 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6785,RMVar_hsa_circ_185471,RMVar_hsa_circ_326675,RMVar_hsa_circ_77547 39824 RMVar_ID_39824 Human_SNP_ID_626825194 A-to-I Human chr17 - 51255181 51255181 51255181 CGCCTCCCGGGTTCAAGTGATTCTTCTGCCTCAGCCTCCCGAGTGGCTGGGACTACAGGCAAATG CGCCTCCCGGGTTCAAGTGATTCTTCTGCCTCGGCCTCCCGAGTGGCTGGGACTACAGGCAAATG T C MBTD1 Ensembl:ENSG00000011258 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1461079777 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6785,RMVar_hsa_circ_185471,RMVar_hsa_circ_326675,RMVar_hsa_circ_77547 39825 RMVar_ID_39825 Human_SNP_ID_626833160 A-to-I Human chr17 + 51281035 51281035 51281035 CCCTGTCTCTGCTAAAAATACAAAAATTAGCCAGGCATGCTGGCGCTCGCCTGTAATCCCAGCTA CCCTGTCTCTGCTAAAAATACAAAAATTAGCCGGGCATGCTGGCGCTCGCCTGTAATCCCAGCTA A G UTP18 Ensembl:ENSG00000011260 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1441309577 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 39826 RMVar_ID_39826 Human_SNP_ID_626833161 A-to-I Human chr17 + 51281035 51281035 51281035 CCCTGTCTCTGCTAAAAATACAAAAATTAGCCAGGCATGCTGGCGCTCGCCTGTAATCCCAGCTA CCCTGTCTCTGCTAAAAATACAAAAATTAGCCTGGCATGCTGGCGCTCGCCTGTAATCCCAGCTA A T UTP18 Ensembl:ENSG00000011260 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1441309577 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 39827 RMVar_ID_39827 Human_SNP_ID_626980665 A-to-I Human chr17 - 51878118 51878118 51878118 TTTTTTTGAGACGGAGTCATGCTCTGTCACCCAGGCTGGAGTGCAGTGGTGCGATCTTGGCTCAC TTTTTTTGAGACGGAGTCATGCTCTGTCACCCGGGCTGGAGTGCAGTGGTGCGATCTTGGCTCAC T C CA10 Ensembl:ENSG00000154975 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1368618375 Functional Loss SNV dbSNP153 33..33 33 - - - 39828 RMVar_ID_39828 Human_SNP_ID_627729095 A-to-I Human chr17 + 54939124 54939124 54939124 GGCTGGGCGCAGTGACTTACATCTGTAATCCTAGCACTTTGGGAGGCCAAGGCACATGGATCACT GGCTGGGCGCAGTGACTTACATCTGTAATCCTTGCACTTTGGGAGGCCAAGGCACATGGATCACT A T TOM1L1 Ensembl:ENSG00000141198 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs528216395 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1559,RMVar_hsa_circ_70062,RMVar_hsa_circ_345242,RMVar_hsa_circ_365200,RMVar_hsa_circ_185492,RMVar_hsa_circ_285757,RMVar_hsa_circ_63541,RMVar_hsa_circ_66690,RMVar_hsa_circ_90767,RMVar_hsa_circ_185503,RMVar_hsa_circ_118146,RMVar_hsa_circ_185498,RMVar_hsa_circ_110179,RMVar_hsa_circ_185499,RMVar_hsa_circ_185501,RMVar_hsa_circ_359999,RMVar_hsa_circ_352491,RMVar_hsa_circ_270943,RMVar_hsa_circ_361911,RMVar_hsa_circ_356738,RMVar_hsa_circ_356287,RMVar_hsa_circ_185504 39829 RMVar_ID_39829 Human_SNP_ID_627729204 A-to-I Human chr17 + 54939696 54939696 54939696 ACTCCCACCTCAACCTCTTAATAGCTGGGACTACAGGTGTGCGCCACCATACTGGGCTAATCTAA ACTCCCACCTCAACCTCTTAATAGCTGGGACTGCAGGTGTGCGCCACCATACTGGGCTAATCTAA A G TOM1L1 Ensembl:ENSG00000141198 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1038966685 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1559,RMVar_hsa_circ_70062,RMVar_hsa_circ_345242,RMVar_hsa_circ_365200,RMVar_hsa_circ_185492,RMVar_hsa_circ_285757,RMVar_hsa_circ_63541,RMVar_hsa_circ_66690,RMVar_hsa_circ_90767,RMVar_hsa_circ_185503,RMVar_hsa_circ_118146,RMVar_hsa_circ_185498,RMVar_hsa_circ_110179,RMVar_hsa_circ_185499,RMVar_hsa_circ_185501,RMVar_hsa_circ_359999,RMVar_hsa_circ_352491,RMVar_hsa_circ_270943,RMVar_hsa_circ_361911,RMVar_hsa_circ_356738,RMVar_hsa_circ_356287,RMVar_hsa_circ_185504 39830 RMVar_ID_39830 Human_SNP_ID_627729285 A-to-I Human chr17 + 54940076 54940076 54940076 TGCCCCAATGCCCAACTAATTTTTGTGTTTTTAGTAGAGGTGAGGTTTTGCCGTGTTGCCCAGGC TGCCCCAATGCCCAACTAATTTTTGTGTTTTTGGTAGAGGTGAGGTTTTGCCGTGTTGCCCAGGC A G TOM1L1 Ensembl:ENSG00000141198 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924259542 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1559,RMVar_hsa_circ_70062,RMVar_hsa_circ_345242,RMVar_hsa_circ_365200,RMVar_hsa_circ_185492,RMVar_hsa_circ_285757,RMVar_hsa_circ_63541,RMVar_hsa_circ_66690,RMVar_hsa_circ_90767,RMVar_hsa_circ_185503,RMVar_hsa_circ_118146,RMVar_hsa_circ_185498,RMVar_hsa_circ_110179,RMVar_hsa_circ_185499,RMVar_hsa_circ_185501,RMVar_hsa_circ_359999,RMVar_hsa_circ_352491,RMVar_hsa_circ_270943,RMVar_hsa_circ_361911,RMVar_hsa_circ_356738,RMVar_hsa_circ_356287,RMVar_hsa_circ_185504 39831 RMVar_ID_39831 Human_SNP_ID_627731269 A-to-I Human chr17 - 54949075 54949074 54949075 TGATCATATGATCATGCTATATATTCTAGCCTAGGTGACTGAATGAGACCCTGTCTCAAAAACAA TGATCATATGATCATGCTATATATTCTAGCCT_GGTGACTGAATGAGACCCTGTCTCAAAAACAA CT C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459018155 Functional Loss DEL dbSNP153 33..33 33 - - - 39832 RMVar_ID_39832 Human_SNP_ID_627732133 A-to-I Human chr17 - 54952425 54952425 54952425 TTTCTGCCTCACCTTCCTGAGTAGCTGGGACTACAGGTGCGCACCACCACACCTGCCTAATTTTT TTTCTGCCTCACCTTCCTGAGTAGCTGGGACTGCAGGTGCGCACCACCACACCTGCCTAATTTTT T C COX11 Ensembl:ENSG00000166260 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs555504905 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13078746 39833 RMVar_ID_39833 Human_SNP_ID_627732332 A-to-I Human chr17 - 54953206 54953206 54953206 CTGGCTGATTTTTTTGTTTGTTTGTGGAGACAAGGTCTCGTTATGCTGTCAGGGCTGGTCTTGAA CTGGCTGATTTTTTTGTTTGTTTGTGGAGACAGGGTCTCGTTATGCTGTCAGGGCTGGTCTTGAA T C COX11 Ensembl:ENSG00000166260 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256663475 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5466713 39834 RMVar_ID_39834 Human_SNP_ID_627733233 A-to-I Human chr17 - 54956720 54956720 54956720 GCATTCTTGGTTGGTTATAGTGGCTCATGCCTATAATCCCAGCACTTTGGAAGGCTGAGGCAGGA GCATTCTTGGTTGGTTATAGTGGCTCATGCCTGTAATCCCAGCACTTTGGAAGGCTGAGGCAGGA T C COX11 Ensembl:ENSG00000166260 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1046935 Functional Loss SNV dbSNP153 33..33 33 - - - 39835 RMVar_ID_39835 Human_SNP_ID_627733237 A-to-I Human chr17 - 54956734 54956734 54956734 ATTGCTCAAAGCCTGCATTCTTGGTTGGTTATAGTGGCTCATGCCTATAATCCCAGCACTTTGGA ATTGCTCAAAGCCTGCATTCTTGGTTGGTTATGGTGGCTCATGCCTATAATCCCAGCACTTTGGA T C COX11 Ensembl:ENSG00000166260 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1011802303 Functional Loss SNV dbSNP153 33..33 33 - - - 39836 RMVar_ID_39836 Human_SNP_ID_627733964 A-to-I Human chr17 - 54959367 54959367 54959367 TTCAAGTGATCCTTCCACTTCAGCCTCTCAAAATGTTGGGATTAGAGGCATAAGCCACCATGCCA TTCAAGTGATCCTTCCACTTCAGCCTCTCAAAGTGTTGGGATTAGAGGCATAAGCCACCATGCCA T C COX11 Ensembl:ENSG00000166260 Protein coding intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs992057176 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13079036 Human_Splice_Rec_1843218 39837 RMVar_ID_39837 Human_SNP_ID_628182654 A-to-I Human chr17 - 56830109 56830109 56830109 CTGATCTCCTGACCTCATGATCCGCCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG CTGATCTCCTGACCTCATGATCCGCCTGCCTCTGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG T A C17orf67 Ensembl:ENSG00000214226 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs147229169 Functional Loss SNV dbSNP153 33..33 33 - - - 39838 RMVar_ID_39838 Human_SNP_ID_628182655 A-to-I Human chr17 - 56830109 56830109 56830109 CTGATCTCCTGACCTCATGATCCGCCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG CTGATCTCCTGACCTCATGATCCGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG T C C17orf67 Ensembl:ENSG00000214226 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs147229169 Functional Loss SNV dbSNP153 33..33 33 - - - 39839 RMVar_ID_39839 Human_SNP_ID_628183205 A-to-I Human chr17 - 56832040 56832040 56832040 TGGGAGGCTTGAGGCAGAGAATTGCTTAACCCAGGAGGCGGAGGTTGCAGTGAGCTGAGATCGCA TGGGAGGCTTGAGGCAGAGAATTGCTTAACCCTGGAGGCGGAGGTTGCAGTGAGCTGAGATCGCA T A C17orf67 Ensembl:ENSG00000214226 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1567803118 Functional Loss SNV dbSNP153 33..33 33 - - - 39840 RMVar_ID_39840 Human_SNP_ID_628183244 A-to-I Human chr17 - 56832212 56832212 56832212 GCCGGGCGCTGTGGCTCACGCCTGTAACCCCAACACTTTGGGAGGCCGAGGCAGGTGCATCACGG GCCGGGCGCTGTGGCTCACGCCTGTAACCCCAGCACTTTGGGAGGCCGAGGCAGGTGCATCACGG T C C17orf67 Ensembl:ENSG00000214226 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1196523085 Functional Loss SNV dbSNP153 33..33 33 - - - 39841 RMVar_ID_39841 Human_SNP_ID_628183247 A-to-I Human chr17 - 56832219 56832219 56832219 TGTTTAGGCCGGGCGCTGTGGCTCACGCCTGTAACCCCAACACTTTGGGAGGCCGAGGCAGGTGC TGTTTAGGCCGGGCGCTGTGGCTCACGCCTGTGACCCCAACACTTTGGGAGGCCGAGGCAGGTGC T C C17orf67 Ensembl:ENSG00000214226 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs537741948 Functional Loss SNV dbSNP153 33..33 33 - - - 39842 RMVar_ID_39842 Human_SNP_ID_628221636 A-to-I Human chr17 + 56984981 56984981 56984981 ATTAGCCGGGCTGGGCATGGTGGTGTGCGCCTATAGTTCCAACTACTTGAGGGGGCTGAGGCGGG ATTAGCCGGGCTGGGCATGGTGGTGTGCGCCTGTAGTTCCAACTACTTGAGGGGGCTGAGGCGGG A G SCPEP1,AC004584.3 Ensembl:ENSG00000121064,Ensembl:ENSG00000263120 Protein coding,lincRNA intron,exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs916654235 Functional Loss SNV dbSNP153 33..33 33 - - - 39843 RMVar_ID_39843 Human_SNP_ID_628237270 A-to-I Human chr17 - 57046016 57046016 57046016 TCCATAGGGTTTGAGTGCAGGACTCCCCAAGGACCCAGGCTGGGGATGGTGGCGGGCGTGATGAT TCCATAGGGTTTGAGTGCAGGACTCCCCAAGGGCCCAGGCTGGGGATGGTGGCGGGCGTGATGAT T C lnc-COIL-1 RNACentral:URS00008C247A lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1165346473 Functional Loss SNV dbSNP153 33..33 33 - - - 39844 RMVar_ID_39844 Human_SNP_ID_628237271 A-to-I Human chr17 - 57046019 57046019 57046019 TAATCCATAGGGTTTGAGTGCAGGACTCCCCAAGGACCCAGGCTGGGGATGGTGGCGGGCGTGAT TAATCCATAGGGTTTGAGTGCAGGACTCCCCAGGGACCCAGGCTGGGGATGGTGGCGGGCGTGAT T C lnc-COIL-1 RNACentral:URS00008C247A lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1460847045 Functional Loss SNV dbSNP153 33..33 33 - - - 39845 RMVar_ID_39845 Human_SNP_ID_628237281 A-to-I Human chr17 - 57046049 57046049 57046049 AAGGCGTCCAGGCCGTTGGCCACTCAGGCGTAATCCATAGGGTTTGAGTGCAGGACTCCCCAAGG AAGGCGTCCAGGCCGTTGGCCACTCAGGCGTAGTCCATAGGGTTTGAGTGCAGGACTCCCCAAGG T C lnc-COIL-1 RNACentral:URS00008C247A lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1211411933 Functional Loss SNV dbSNP153 33..33 33 - - - 39846 RMVar_ID_39846 Human_SNP_ID_628251895 A-to-I Human chr17 + 57102969 57102969 57102969 AAGTGTGGTGGTGGGCGCCTGTAGACCCAGCTACTCTGGAGGCTGAGACAGGAGAACTGCATGAA AAGTGTGGTGGTGGGCGCCTGTAGACCCAGCTGCTCTGGAGGCTGAGACAGGAGAACTGCATGAA A G AKAP1 Ensembl:ENSG00000121057 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946076473 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8457607,Human_RBP_ID_17566042,Human_RBP_ID_22717460 39847 RMVar_ID_39847 Human_SNP_ID_628325248 A-to-I Human chr17 + 57412091 57412091 57412091 CTGACCTTCCTCTCTGTCACCCAGGCTAGAGTATAGTGGCGCGACCTCAGCTCACTGCAACCTCT CTGACCTTCCTCTCTGTCACCCAGGCTAGAGTGTAGTGGCGCGACCTCAGCTCACTGCAACCTCT A G MSI2 Ensembl:ENSG00000153944 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1241256366 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 39848 RMVar_ID_39848 Human_SNP_ID_628335838 A-to-I Human chr17 + 57456475 57456475 57456475 ACTATTAGTGGGGCGTGGTGGCAGGCACCTGTAATCCCAGCTACTCAGGAGGCGGAGGCAGAGAA ACTATTAGTGGGGCGTGGTGGCAGGCACCTGTGATCCCAGCTACTCAGGAGGCGGAGGCAGAGAA A G MSI2 Ensembl:ENSG00000153944 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1349155979 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 39849 RMVar_ID_39849 Human_SNP_ID_628337133 A-to-I Human chr17 + 57461754 57461754 57461754 ACAGGTTTCACCATGTTGGCCAGACTGGTCTCAAACTCCTGACCTCAAGAGATCTGCTACCTCGG ACAGGTTTCACCATGTTGGCCAGACTGGTCTCGAACTCCTGACCTCAAGAGATCTGCTACCTCGG A G MSI2 Ensembl:ENSG00000153944 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1157029435 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 39850 RMVar_ID_39850 Human_SNP_ID_628337145 A-to-I Human chr17 + 57461798 57461798 57461798 TCAAGAGATCTGCTACCTCGGCCTCCCAAAGTACTGGGATTACAGACGTGAGCTAGAACCCTTGG TCAAGAGATCTGCTACCTCGGCCTCCCAAAGTGCTGGGATTACAGACGTGAGCTAGAACCCTTGG A G MSI2 Ensembl:ENSG00000153944 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1567838112 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 39851 RMVar_ID_39851 Human_SNP_ID_628428314 A-to-I Human chr17 - 57841884 57841884 57841884 GGAGTGCAATGGTGCGCTCTCCACTTACTGCAACCTCTGCCTCCTGGGTTCAAGTGATTCTCCCA GGAGTGCAATGGTGCGCTCTCCACTTACTGCACCCTCTGCCTCCTGGGTTCAAGTGATTCTCCCA T G MRPS23 Ensembl:ENSG00000181610 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1177274173 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18689,RMVar_hsa_circ_111978,RMVar_hsa_circ_185596,RMVar_hsa_circ_103421,RMVar_hsa_circ_185595 39852 RMVar_ID_39852 Human_SNP_ID_628428384 A-to-I Human chr17 - 57842150 57842150 57842150 CTTAGCCAGGCATGGTGGTGCTGCGAACCTGTAGTTCCAGCTACTCAGGATGCTGAGGCAAGAGG CTTAGCCAGGCATGGTGGTGCTGCGAACCTGTGGTTCCAGCTACTCAGGATGCTGAGGCAAGAGG T C MRPS23 Ensembl:ENSG00000181610 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1392209366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6618864 RMVar_hsa_circ_18689,RMVar_hsa_circ_111978,RMVar_hsa_circ_185596,RMVar_hsa_circ_103421,RMVar_hsa_circ_185595 39853 RMVar_ID_39853 Human_SNP_ID_628429040 A-to-I Human chr17 - 57844268 57844268 57844268 TAGAGTGGTTGTGCATGCCTGTAGTTCCAGCTACTTGGGAGGCTGAGGAAGGAGGACCATTGGAG TAGAGTGGTTGTGCATGCCTGTAGTTCCAGCTGCTTGGGAGGCTGAGGAAGGAGGACCATTGGAG T C MRPS23 Ensembl:ENSG00000181610 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs986902526 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6618874 RMVar_hsa_circ_18689,RMVar_hsa_circ_111978,RMVar_hsa_circ_185596,RMVar_hsa_circ_103421,RMVar_hsa_circ_185595 39854 RMVar_ID_39854 Human_SNP_ID_628429043 A-to-I Human chr17 - 57844278 57844278 57844278 AAAAAGCTTATAGAGTGGTTGTGCATGCCTGTAGTTCCAGCTACTTGGGAGGCTGAGGAAGGAGG AAAAAGCTTATAGAGTGGTTGTGCATGCCTGTGGTTCCAGCTACTTGGGAGGCTGAGGAAGGAGG T C MRPS23 Ensembl:ENSG00000181610 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1379966810 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6618874 RMVar_hsa_circ_18689,RMVar_hsa_circ_111978,RMVar_hsa_circ_185596,RMVar_hsa_circ_103421,RMVar_hsa_circ_185595 39855 RMVar_ID_39855 Human_SNP_ID_628430216 A-to-I Human chr17 - 57847890 57847890 57847890 GAGTTCGAGACCACCTTGGGCAATATGGTGAAACCCTGTCTTGACTAAAATACCAAAAATTAGCC GAGTTCGAGACCACCTTGGGCAATATGGTGAAGCCCTGTCTTGACTAAAATACCAAAAATTAGCC T C MRPS23 Ensembl:ENSG00000181610 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs543604817 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6618882 RMVar_hsa_circ_18689,RMVar_hsa_circ_111978,RMVar_hsa_circ_185596,RMVar_hsa_circ_103421,RMVar_hsa_circ_185595 39856 RMVar_ID_39856 Human_SNP_ID_628460969 A-to-I Human chr17 - 57972462 57972462 57972462 GTGTGGACTACTGGAAGGACTCGTGTAGGGAAAGCCCAAGAATGACCTTGCTGAGGCCTGGATTG GTGTGGACTACTGGAAGGACTCGTGTAGGGAATGCCCAAGAATGACCTTGCTGAGGCCTGGATTG T A VEZF1 Ensembl:ENSG00000136451 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository;ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs986022706 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_495065,Human_RBP_ID_3529815,Human_RBP_ID_8458015,Human_RBP_ID_8947857,Human_RBP_ID_18703523,Human_RBP_ID_21890235,Human_RBP_ID_23737951,Human_RBP_ID_26453588 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 39857 RMVar_ID_39857 Human_SNP_ID_628460970 A-to-I Human chr17 - 57972462 57972462 57972462 GTGTGGACTACTGGAAGGACTCGTGTAGGGAAAGCCCAAGAATGACCTTGCTGAGGCCTGGATTG GTGTGGACTACTGGAAGGACTCGTGTAGGGAACGCCCAAGAATGACCTTGCTGAGGCCTGGATTG T G VEZF1 Ensembl:ENSG00000136451 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository;ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs986022706 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_495065,Human_RBP_ID_3529815,Human_RBP_ID_8458015,Human_RBP_ID_8947857,Human_RBP_ID_18703523,Human_RBP_ID_21890235,Human_RBP_ID_23737951,Human_RBP_ID_26453588 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 39858 RMVar_ID_39858 Human_SNP_ID_628460971 A-to-I Human chr17 - 57972463 57972463 57972463 TGTGTGGACTACTGGAAGGACTCGTGTAGGGAAAGCCCAAGAATGACCTTGCTGAGGCCTGGATT TGTGTGGACTACTGGAAGGACTCGTGTAGGGAGAGCCCAAGAATGACCTTGCTGAGGCCTGGATT T C VEZF1 Ensembl:ENSG00000136451 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1136678 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_495065,Human_RBP_ID_3529815,Human_RBP_ID_8458015,Human_RBP_ID_8947857,Human_RBP_ID_13092091,Human_RBP_ID_18703523,Human_RBP_ID_21890235,Human_RBP_ID_23737951,Human_RBP_ID_26453588 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 39859 RMVar_ID_39859 Human_SNP_ID_628460972 A-to-I Human chr17 - 57972468 57972468 57972468 CATTATGTGTGGACTACTGGAAGGACTCGTGTAGGGAAAGCCCAAGAATGACCTTGCTGAGGCCT CATTATGTGTGGACTACTGGAAGGACTCGTGTGGGGAAAGCCCAAGAATGACCTTGCTGAGGCCT T C VEZF1 Ensembl:ENSG00000136451 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11839 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_495065,Human_RBP_ID_3529815,Human_RBP_ID_4440932,Human_RBP_ID_8458015,Human_RBP_ID_8947857,Human_RBP_ID_13092091,Human_RBP_ID_18703523,Human_RBP_ID_21890235,Human_RBP_ID_23737951,Human_RBP_ID_26453588 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 39860 RMVar_ID_39860 Human_SNP_ID_628462140 A-to-I Human chr17 - 57977233 57977231 57977234 GCGTGTCTGTAGTCCCCGCTACTCAGGAAGCTAAGGTGGGAGGGTCACTTGAACCCAGGAGTTTG GCGTGTCTGTAGTCCCCGCTACTCAGGAAGC___GGTGGGAGGGTCACTTGAACCCAGGAGTTTG CTTA C VEZF1 Ensembl:ENSG00000136451 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559332079 Functional Loss DEL dbSNP153 32..34 33 - - - 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 39861 RMVar_ID_39861 Human_SNP_ID_628462141 A-to-I Human chr17 - 57977233 57977233 57977233 GCGTGTCTGTAGTCCCCGCTACTCAGGAAGCTAAGGTGGGAGGGTCACTTGAACCCAGGAGTTTG GCGTGTCTGTAGTCCCCGCTACTCAGGAAGCTGAGGTGGGAGGGTCACTTGAACCCAGGAGTTTG T C VEZF1 Ensembl:ENSG00000136451 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1051798265 Functional Loss SNV dbSNP153 33..33 33 - - - 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 39862 RMVar_ID_39862 Human_SNP_ID_628493116 A-to-I Human chr17 + 58100126 58100126 58100126 GCAGCACACTGTAGCCTCAACCTCCTGTGTTCAAGCCATCTTCCCACCTCAGCCTCCCAAGTAGC GCAGCACACTGTAGCCTCAACCTCCTGTGTTCGAGCCATCTTCCCACCTCAGCCTCCCAAGTAGC A G AC015813.6 Ensembl:ENSG00000279207 Other exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1340576614 Functional Loss SNV dbSNP153 33..33 33 - - - 39863 RMVar_ID_39863 Human_SNP_ID_628554308 A-to-I Human chr17 + 58341681 58341681 58341681 ATAAAAGGCCGGACGCAGTGGCTCATGCCTGTAGTCCCAGCAGTTTGGGAGGCCGAGGTGGGTGG ATAAAAGGCCGGACGCAGTGGCTCATGCCTGTGGTCCCAGCAGTTTGGGAGGCCGAGGTGGGTGG A G TSPOAP1-AS1 Ensembl:ENSG00000265148 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs939737777 Functional Loss SNV dbSNP153 33..33 33 - - - 39864 RMVar_ID_39864 Human_SNP_ID_628557612 A-to-I Human chr17 - 58354276 58354276 58354276 AGCAGCCTTGGTTCCTCTGGGGGTTGAGAATAAGAATAGTGGGGAGGGAAAAACTCCTCCTTGAA AGCAGCCTTGGTTCCTCTGGGGGTTGAGAATAGGAATAGTGGGGAGGGAAAAACTCCTCCTTGAA T C RNF43,AC004687.2 Ensembl:ENSG00000108375,Ensembl:ENSG00000285897 Protein coding,Protein coding 3'UTR,intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1247144319 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3530161,Human_RBP_ID_22954922 39865 RMVar_ID_39865 Human_SNP_ID_628572657 A-to-I Human chr17 - 58424490 58424490 58424490 CTCCTGCCTCAGCCTCCCTGGTGGCTGGGACTACAGGCGCCTGCCACCATGCCCAACTAATTTTT CTCCTGCCTCAGCCTCCCTGGTGGCTGGGACTGCAGGCGCCTGCCACCATGCCCAACTAATTTTT T C HSF5 Ensembl:ENSG00000176160 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1423168614 Functional Loss SNV dbSNP153 33..33 33 - - - 39866 RMVar_ID_39866 Human_SNP_ID_628584156 A-to-I Human chr17 - 58476373 58476373 58476373 CAGCATGAGGAACCAGGGAGCTTCTTTACCTGATTTACTGACCATTCTGATGCAGGTACTGATGA CAGCATGAGGAACCAGGGAGCTTCTTTACCTGGTTTACTGACCATTCTGATGCAGGTACTGATGA T C SETP3,HSF5 Ensembl:ENSG00000266648,Ensembl:ENSG00000176160 Pseudogene,Protein coding exon,intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs761907076 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_355749 39867 RMVar_ID_39867 Human_SNP_ID_628589741 A-to-I Human chr17 - 58499523 58499523 58499523 TGGATACATGAGAGGTAGGGTTTTCTCGCTCCATTGCCCAGCTGGAGTGCAGTCACATGATCTTC TGGATACATGAGAGGTAGGGTTTTCTCGCTCCTTTGCCCAGCTGGAGTGCAGTCACATGATCTTC T A MTMR4 Ensembl:ENSG00000108389 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1271114301 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17566950 RMVar_hsa_circ_82114,RMVar_hsa_circ_108677,RMVar_hsa_circ_125609,RMVar_hsa_circ_125851,RMVar_hsa_circ_117954,RMVar_hsa_circ_90165,RMVar_hsa_circ_99160,RMVar_hsa_circ_82633,RMVar_hsa_circ_93589,RMVar_hsa_circ_185649,RMVar_hsa_circ_185651,RMVar_hsa_circ_185652,RMVar_hsa_circ_185653,RMVar_hsa_circ_185650,RMVar_hsa_circ_185647,RMVar_hsa_circ_185648,RMVar_hsa_circ_185646,RMVar_hsa_circ_185654,RMVar_hsa_circ_48209 39868 RMVar_ID_39868 Human_SNP_ID_628589911 A-to-I Human chr17 - 58500219 58500219 58500219 GGAGGGCTGACGTAGGAGGATTGTTTGCTCCCAGCAGGTTGAGGCTGCAGTGAGCTGTGATCATG GGAGGGCTGACGTAGGAGGATTGTTTGCTCCCTGCAGGTTGAGGCTGCAGTGAGCTGTGATCATG T A MTMR4 Ensembl:ENSG00000108389 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs142668344 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82114,RMVar_hsa_circ_108677,RMVar_hsa_circ_125609,RMVar_hsa_circ_125851,RMVar_hsa_circ_117954,RMVar_hsa_circ_90165,RMVar_hsa_circ_99160,RMVar_hsa_circ_82633,RMVar_hsa_circ_93589,RMVar_hsa_circ_185649,RMVar_hsa_circ_185651,RMVar_hsa_circ_185652,RMVar_hsa_circ_185653,RMVar_hsa_circ_185650,RMVar_hsa_circ_185647,RMVar_hsa_circ_185648,RMVar_hsa_circ_185646,RMVar_hsa_circ_185654,RMVar_hsa_circ_48209 39869 RMVar_ID_39869 Human_SNP_ID_628590303 A-to-I Human chr17 - 58501893 58501893 58501893 CACCATGCCCAGCTAATTTTTGTATTTGTAGTAGAGACGGGGTTTTACCATGTTGGTCACACTGG CACCATGCCCAGCTAATTTTTGTATTTGTAGTTGAGACGGGGTTTTACCATGTTGGTCACACTGG T A MTMR4 Ensembl:ENSG00000108389 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1245892180 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82114,RMVar_hsa_circ_108677,RMVar_hsa_circ_125609,RMVar_hsa_circ_125851,RMVar_hsa_circ_117954,RMVar_hsa_circ_90165,RMVar_hsa_circ_99160,RMVar_hsa_circ_82633,RMVar_hsa_circ_93589,RMVar_hsa_circ_185649,RMVar_hsa_circ_185651,RMVar_hsa_circ_185652,RMVar_hsa_circ_185653,RMVar_hsa_circ_185650,RMVar_hsa_circ_185647,RMVar_hsa_circ_185648,RMVar_hsa_circ_185646,RMVar_hsa_circ_185654,RMVar_hsa_circ_48209 39870 RMVar_ID_39870 Human_SNP_ID_628595928 A-to-I Human chr17 - 58524767 58524767 58524767 GGCCAGGAGTTCAAGGCCAGCCTGGGCAACATAGTAAGATCCCATCTCTACAAAAAGTTTTAAAA GGCCAGGAGTTCAAGGCCAGCCTGGGCAACATTGTAAGATCCCATCTCTACAAAAAGTTTTAAAA T A SEPTIN4 Ensembl:ENSG00000108387 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1165201138 Functional Loss SNV dbSNP153 33..33 33 - - - 39871 RMVar_ID_39871 Human_SNP_ID_628620892 A-to-I Human chr17 - 58626374 58626374 58626374 TTTAGTAGAGACGGGGTTTCACCATGTTGGCTAAGCTGGTCTCGAACTCCTGACCTCAGATGATC TTTAGTAGAGACGGGGTTTCACCATGTTGGCTTAGCTGGTCTCGAACTCCTGACCTCAGATGATC T A TEX14 Ensembl:ENSG00000121101 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs981991512 Functional Loss SNV dbSNP153 33..33 33 - - - 39872 RMVar_ID_39872 Human_SNP_ID_628620893 A-to-I Human chr17 - 58626383 58626383 58626383 GTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCTAAGCTGGTCTCGAACTCCTGACCT GTTTGTATTTTTAGTAGAGACGGGGTTTCACCGTGTTGGCTAAGCTGGTCTCGAACTCCTGACCT T C TEX14 Ensembl:ENSG00000121101 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1258303289 Functional Loss SNV dbSNP153 33..33 33 - - - 39873 RMVar_ID_39873 Human_SNP_ID_628640808 A-to-I Human chr17 + 58697735 58697734 58697736 TGACTGTAAAACGATTTTTTTTTTTTTGAGACAAAGTTTCGCTTTTGCTGCCCAGGCTGGAGTGC TGACTGTAAAACGATTTTTTTTTTTTTGAGAC__AGTTTCGCTTTTGCTGCCCAGGCTGGAGTGC CAA C RAD51C Ensembl:ENSG00000108384 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1442005894 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_185665,RMVar_hsa_circ_276174,RMVar_hsa_circ_342903,RMVar_hsa_circ_185664,RMVar_hsa_circ_77761,RMVar_hsa_circ_185663,RMVar_hsa_circ_67540,RMVar_hsa_circ_325139,RMVar_hsa_circ_306304,RMVar_hsa_circ_185666 39874 RMVar_ID_39874 Human_SNP_ID_628640809 A-to-I Human chr17 + 58697735 58697735 58697735 TGACTGTAAAACGATTTTTTTTTTTTTGAGACAAAGTTTCGCTTTTGCTGCCCAGGCTGGAGTGC TGACTGTAAAACGATTTTTTTTTTTTTGAGACGAAGTTTCGCTTTTGCTGCCCAGGCTGGAGTGC A G RAD51C Ensembl:ENSG00000108384 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1261710374 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_185665,RMVar_hsa_circ_276174,RMVar_hsa_circ_342903,RMVar_hsa_circ_185664,RMVar_hsa_circ_77761,RMVar_hsa_circ_185663,RMVar_hsa_circ_67540,RMVar_hsa_circ_325139,RMVar_hsa_circ_306304,RMVar_hsa_circ_185666 39875 RMVar_ID_39875 Human_SNP_ID_628641932 A-to-I Human chr17 + 58701839 58701839 58701839 ATCCACCCAGCTTCCCAAAGTGCTGTGATTACAAGTGTGAGCCACCACGCCCAGCCTCAAACTGT ATCCACCCAGCTTCCCAAAGTGCTGTGATTACGAGTGTGAGCCACCACGCCCAGCCTCAAACTGT A G RAD51C Ensembl:ENSG00000108384 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs751088727 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_185665,RMVar_hsa_circ_276174,RMVar_hsa_circ_342903,RMVar_hsa_circ_185664,RMVar_hsa_circ_77761,RMVar_hsa_circ_185663,RMVar_hsa_circ_67540,RMVar_hsa_circ_325139,RMVar_hsa_circ_306304,RMVar_hsa_circ_185666 39876 RMVar_ID_39876 Human_SNP_ID_628645073 A-to-I Human chr17 + 58713545 58713545 58713545 AAATTTTTTGTAGAGGCTGGGCACGGTGGCTCACACCTATAACCCACCACTGTGGGAGGCCAGGG AAATTTTTTGTAGAGGCTGGGCACGGTGGCTCGCACCTATAACCCACCACTGTGGGAGGCCAGGG A G RAD51C Ensembl:ENSG00000108384 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1252968849 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_235795 RMVar_hsa_circ_342903,RMVar_hsa_circ_185664,RMVar_hsa_circ_77761,RMVar_hsa_circ_325139,RMVar_hsa_circ_185666,RMVar_hsa_circ_303305,RMVar_hsa_circ_365069,RMVar_hsa_circ_185668,RMVar_hsa_circ_43997,RMVar_hsa_circ_355498,RMVar_hsa_circ_94496,RMVar_hsa_circ_364600,RMVar_hsa_circ_185669 39877 RMVar_ID_39877 Human_SNP_ID_628645086 A-to-I Human chr17 + 58713646 58713644 58713647 CCTTGCCAACATGGTGAAACCTTGTCTCTACTAATAATACAAAAATTAGCCAGGTGTGTTGGTGC CCTTGCCAACATGGTGAAACCTTGTCTCTAC___TAATACAAAAATTAGCCAGGTGTGTTGGTGC CTAA C RAD51C Ensembl:ENSG00000108384 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1307277585 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_342903,RMVar_hsa_circ_185664,RMVar_hsa_circ_77761,RMVar_hsa_circ_325139,RMVar_hsa_circ_185666,RMVar_hsa_circ_303305,RMVar_hsa_circ_365069,RMVar_hsa_circ_185668,RMVar_hsa_circ_43997,RMVar_hsa_circ_355498,RMVar_hsa_circ_94496,RMVar_hsa_circ_364600,RMVar_hsa_circ_185669 39878 RMVar_ID_39878 Human_SNP_ID_628646091 A-to-I Human chr17 + 58717629 58717629 58717629 ATGGTAGCTCACACCTGTAATCCCAGCTACTCATGAGGCTGAGGCAGGGGAATCGCTTGAACTCA ATGGTAGCTCACACCTGTAATCCCAGCTACTCGTGAGGCTGAGGCAGGGGAATCGCTTGAACTCA A G RAD51C Ensembl:ENSG00000108384 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1307337745 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_342903,RMVar_hsa_circ_185664,RMVar_hsa_circ_77761,RMVar_hsa_circ_325139,RMVar_hsa_circ_185666,RMVar_hsa_circ_303305,RMVar_hsa_circ_365069,RMVar_hsa_circ_185668,RMVar_hsa_circ_43997,RMVar_hsa_circ_355498,RMVar_hsa_circ_94496,RMVar_hsa_circ_364600,RMVar_hsa_circ_185669 39879 RMVar_ID_39879 Human_SNP_ID_628646814 A-to-I Human chr17 + 58720572 58720572 58720572 GGCTCACTGCAACCTCTGCCTGCCCCAGGTTCAAATGATTCTCCTGCCTCAGCCTCCGGAGTAGC GGCTCACTGCAACCTCTGCCTGCCCCAGGTTCCAATGATTCTCCTGCCTCAGCCTCCGGAGTAGC A C RAD51C Ensembl:ENSG00000108384 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1039869354 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_342903,RMVar_hsa_circ_185664,RMVar_hsa_circ_77761,RMVar_hsa_circ_325139,RMVar_hsa_circ_185666,RMVar_hsa_circ_303305,RMVar_hsa_circ_365069,RMVar_hsa_circ_185668,RMVar_hsa_circ_43997,RMVar_hsa_circ_355498,RMVar_hsa_circ_94496,RMVar_hsa_circ_364600,RMVar_hsa_circ_185669 39880 RMVar_ID_39880 Human_SNP_ID_628646827 A-to-I Human chr17 + 58720612 58720612 58720612 CTCCTGCCTCAGCCTCCGGAGTAGCTGGGATTACAGGTGCATGCCACCATGTCTGGTTAATTTTT CTCCTGCCTCAGCCTCCGGAGTAGCTGGGATTGCAGGTGCATGCCACCATGTCTGGTTAATTTTT A G RAD51C Ensembl:ENSG00000108384 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1226273648 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_342903,RMVar_hsa_circ_185664,RMVar_hsa_circ_77761,RMVar_hsa_circ_325139,RMVar_hsa_circ_185666,RMVar_hsa_circ_303305,RMVar_hsa_circ_365069,RMVar_hsa_circ_185668,RMVar_hsa_circ_43997,RMVar_hsa_circ_355498,RMVar_hsa_circ_94496,RMVar_hsa_circ_364600,RMVar_hsa_circ_185669 39881 RMVar_ID_39881 Human_SNP_ID_628649163 A-to-I Human chr17 + 58729806 58729806 58729806 TTTGACCAGGCTGGTCTCGGATGCCTGACCTCAAGTGACCTGCCCACCTCAGCCTCCCAAAGTGC TTTGACCAGGCTGGTCTCGGATGCCTGACCTCCAGTGACCTGCCCACCTCAGCCTCCCAAAGTGC A C RAD51C Ensembl:ENSG00000108384 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1226468418 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13095569 RMVar_hsa_circ_94496,RMVar_hsa_circ_185669 39882 RMVar_ID_39882 Human_SNP_ID_628658203 A-to-I Human chr17 + 58768348 58768348 58768348 GTGATCCACCCACCTTGGCCTCCCAAAGTGCTAGGATTGTAGGTATGAGCTACCTTGCCTGGCCC GTGATCCACCCACCTTGGCCTCCCAAAGTGCTGGGATTGTAGGTATGAGCTACCTTGCCTGGCCC A G PPM1E Ensembl:ENSG00000175175 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1016753666 Functional Loss SNV dbSNP153 33..33 33 - - - 39883 RMVar_ID_39883 Human_SNP_ID_628660276 A-to-I Human chr17 + 58777053 58777053 58777053 CTGGAGTTTGAGACCAGCCTGGGCAACATAGCAAGTCCCCGGCTTTACAAAAAAAATTAACCAGG CTGGAGTTTGAGACCAGCCTGGGCAACATAGCTAGTCCCCGGCTTTACAAAAAAAATTAACCAGG A T PPM1E Ensembl:ENSG00000175175 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1009388390 Functional Loss SNV dbSNP153 33..33 33 - - - 39884 RMVar_ID_39884 Human_SNP_ID_628660286 A-to-I Human chr17 + 58777092 58777092 58777092 CGGCTTTACAAAAAAAATTAACCAGGCATGGTAGTGCCTGCCTGTACTCCTAGCTACATGGCAGG CGGCTTTACAAAAAAAATTAACCAGGCATGGTGGTGCCTGCCTGTACTCCTAGCTACATGGCAGG A G PPM1E Ensembl:ENSG00000175175 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1033318917 Functional Loss SNV dbSNP153 33..33 33 - - - 39885 RMVar_ID_39885 Human_SNP_ID_628662969 A-to-I Human chr17 + 58788358 58788358 58788358 TATAAACTCTTTCTTTCCTTGATTTTCATCCAAAGAGTTAGAGTGTATACAGATTAACAAGGTGA TATAAACTCTTTCTTTCCTTGATTTTCATCCAGAGAGTTAGAGTGTATACAGATTAACAAGGTGA A G PPM1E Ensembl:ENSG00000175175 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1444193475 Functional Loss SNV dbSNP153 33..33 33 - - - 39886 RMVar_ID_39886 Human_SNP_ID_628682299 A-to-I Human chr17 + 58871636 58871636 58871636 TAGGAGTTTGAGATCAGACTGGACAATATGGCAAAACTCCGTCTCTACAAACAATACAAAAAATT TAGGAGTTTGAGATCAGACTGGACAATATGGCGAAACTCCGTCTCTACAAACAATACAAAAAATT A G PPM1E Ensembl:ENSG00000175175 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1301733033 Functional Loss SNV dbSNP153 33..33 33 - - - 39887 RMVar_ID_39887 Human_SNP_ID_628712295 A-to-I Human chr17 - 59004065 59004065 59004065 GTGTTCTGTTACCTAGGCTGGAGTACAGTGGTACAATCATAGCTCACTGCAGGCTTGAACTCCTG GTGTTCTGTTACCTAGGCTGGAGTACAGTGGTGCAATCATAGCTCACTGCAGGCTTGAACTCCTG T C TRIM37 Ensembl:ENSG00000108395 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs779459166 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6622058 RMVar_hsa_circ_62481,RMVar_hsa_circ_332257,RMVar_hsa_circ_86591,RMVar_hsa_circ_185681,RMVar_hsa_circ_355629,RMVar_hsa_circ_276692,RMVar_hsa_circ_313386,RMVar_hsa_circ_185683,RMVar_hsa_circ_2943,RMVar_hsa_circ_56486,RMVar_hsa_circ_2033,RMVar_hsa_circ_32380,RMVar_hsa_circ_185682 39888 RMVar_ID_39888 Human_SNP_ID_628713901 A-to-I Human chr17 - 59010651 59010650 59010652 TCATCTCTACTAAATATAGAAATATTAGCCAGATGTGGTAGCAGACACCTGTAATCCCAGCTACT TCATCTCTACTAAATATAGAAATATTAGCCA__TGTGGTAGCAGACACCTGTAATCCCAGCTACT ATC A TRIM37 Ensembl:ENSG00000108395 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1318009092 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_62481,RMVar_hsa_circ_332257,RMVar_hsa_circ_86591,RMVar_hsa_circ_185681,RMVar_hsa_circ_355629,RMVar_hsa_circ_276692,RMVar_hsa_circ_313386,RMVar_hsa_circ_185683,RMVar_hsa_circ_2943,RMVar_hsa_circ_56486,RMVar_hsa_circ_2033,RMVar_hsa_circ_32380,RMVar_hsa_circ_185682 39889 RMVar_ID_39889 Human_SNP_ID_628720128 A-to-I Human chr17 - 59035572 59035572 59035572 CTAATTTTTGTATTTTTAGTAGAGACGGTTTCACCATTGTGGCCAGGCTGGTCTTGAACTCCTGA CTAATTTTTGTATTTTTAGTAGAGACGGTTTCGCCATTGTGGCCAGGCTGGTCTTGAACTCCTGA T C TRIM37 Ensembl:ENSG00000108395 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs538323260 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39,RMVar_hsa_circ_25246,RMVar_hsa_circ_355629,RMVar_hsa_circ_313386,RMVar_hsa_circ_56486,RMVar_hsa_circ_2033,RMVar_hsa_circ_311895,RMVar_hsa_circ_185682,RMVar_hsa_circ_349141,RMVar_hsa_circ_316834,RMVar_hsa_circ_33718,RMVar_hsa_circ_32506,RMVar_hsa_circ_185689,RMVar_hsa_circ_18381,RMVar_hsa_circ_185688,RMVar_hsa_circ_185692,RMVar_hsa_circ_315953,RMVar_hsa_circ_321590,RMVar_hsa_circ_352908,RMVar_hsa_circ_314964,RMVar_hsa_circ_268418,RMVar_hsa_circ_284542,RMVar_hsa_circ_185693,RMVar_hsa_circ_185691,RMVar_hsa_circ_292154,RMVar_hsa_circ_304092,RMVar_hsa_circ_103786,RMVar_hsa_circ_8750,RMVar_hsa_circ_333211,RMVar_hsa_circ_185694,RMVar_hsa_circ_185695,RMVar_hsa_circ_375375,RMVar_hsa_circ_378738,RMVar_hsa_circ_344996,RMVar_hsa_circ_98405,RMVar_hsa_circ_306225,RMVar_hsa_circ_37569,RMVar_hsa_circ_185696,RMVar_hsa_circ_185698,RMVar_hsa_circ_185700,RMVar_hsa_circ_185701,RMVar_hsa_circ_185699,RMVar_hsa_circ_185697,RMVar_hsa_circ_28748,RMVar_hsa_circ_300102,RMVar_hsa_circ_339936,RMVar_hsa_circ_378302,RMVar_hsa_circ_333178,RMVar_hsa_circ_106105,RMVar_hsa_circ_9794,RMVar_hsa_circ_185702,RMVar_hsa_circ_185703 39890 RMVar_ID_39890 Human_SNP_ID_628722657 A-to-I Human chr17 - 59044378 59044378 59044378 TTTTGTAGTTTTAGTAGAGACAGGGTTTTGCAATGTTGACCAGGCTGGTTTTGAACTCCTGGCCT TTTTGTAGTTTTAGTAGAGACAGGGTTTTGCAGTGTTGACCAGGCTGGTTTTGAACTCCTGGCCT T C TRIM37 Ensembl:ENSG00000108395 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1345556151 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13099215 RMVar_hsa_circ_39,RMVar_hsa_circ_25246,RMVar_hsa_circ_313386,RMVar_hsa_circ_56486,RMVar_hsa_circ_2033,RMVar_hsa_circ_185682,RMVar_hsa_circ_349141,RMVar_hsa_circ_316834,RMVar_hsa_circ_33718,RMVar_hsa_circ_32506,RMVar_hsa_circ_185689,RMVar_hsa_circ_18381,RMVar_hsa_circ_185692,RMVar_hsa_circ_315953,RMVar_hsa_circ_321590,RMVar_hsa_circ_352908,RMVar_hsa_circ_268418,RMVar_hsa_circ_284542,RMVar_hsa_circ_185693,RMVar_hsa_circ_292154,RMVar_hsa_circ_304092,RMVar_hsa_circ_8750,RMVar_hsa_circ_185695,RMVar_hsa_circ_375375,RMVar_hsa_circ_378738,RMVar_hsa_circ_344996,RMVar_hsa_circ_98405,RMVar_hsa_circ_306225,RMVar_hsa_circ_37569,RMVar_hsa_circ_185696,RMVar_hsa_circ_185698,RMVar_hsa_circ_185700,RMVar_hsa_circ_185699,RMVar_hsa_circ_185697,RMVar_hsa_circ_28748,RMVar_hsa_circ_300102,RMVar_hsa_circ_339936,RMVar_hsa_circ_378302,RMVar_hsa_circ_333178,RMVar_hsa_circ_106105,RMVar_hsa_circ_185709,RMVar_hsa_circ_320692,RMVar_hsa_circ_350804,RMVar_hsa_circ_185702,RMVar_hsa_circ_185703,RMVar_hsa_circ_362550,RMVar_hsa_circ_371211,RMVar_hsa_circ_335074,RMVar_hsa_circ_350749,RMVar_hsa_circ_325486,RMVar_hsa_circ_270162,RMVar_hsa_circ_281225,RMVar_hsa_circ_22024,RMVar_hsa_circ_185705,RMVar_hsa_circ_185707,RMVar_hsa_circ_185708,RMVar_hsa_circ_185706,RMVar_hsa_circ_185704 39891 RMVar_ID_39891 Human_SNP_ID_628735313 A-to-I Human chr17 - 59094121 59094121 59094121 GGGAGGCCCAGGCGGGCAGATCACTTGAGGTCAGAGTTGGAGACTAGCCTGGCCAACGTGGGAAA GGGAGGCCCAGGCGGGCAGATCACTTGAGGTCGGAGTTGGAGACTAGCCTGGCCAACGTGGGAAA T C TRIM37 Ensembl:ENSG00000108395 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559562998 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13100225 RMVar_hsa_circ_375375,RMVar_hsa_circ_185696,RMVar_hsa_circ_376507,RMVar_hsa_circ_41589,RMVar_hsa_circ_17756,RMVar_hsa_circ_325782,RMVar_hsa_circ_185757,RMVar_hsa_circ_280100 39892 RMVar_ID_39892 Human_SNP_ID_628742431 A-to-I Human chr17 - 59122331 59122331 59122331 GCTGGGACTTGCAGGCGTGAGTCACTGCACCCAGCCTTTGAATTATTTTTTGTAGAGATGAGGTT GCTGGGACTTGCAGGCGTGAGTCACTGCACCCGGCCTTTGAATTATTTTTTGTAGAGATGAGGTT T C SKA2 Ensembl:ENSG00000182628 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1291128330 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5402,RMVar_hsa_circ_341275 39893 RMVar_ID_39893 Human_SNP_ID_628742696 A-to-I Human chr17 - 59123324 59123324 59123324 TCACACTCCTGACCTCATGATCCACCCGCTTCAGCTTCCCAAAGTGCTGGGATTACAGGCATTAG TCACACTCCTGACCTCATGATCCACCCGCTTCTGCTTCCCAAAGTGCTGGGATTACAGGCATTAG T A SKA2 Ensembl:ENSG00000182628 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1451831989 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5402,RMVar_hsa_circ_341275 39894 RMVar_ID_39894 Human_SNP_ID_628743683 A-to-I Human chr17 - 59127510 59127510 59127510 GTGGCACGAGCCTGTAACCCCAGCTACTTGGGAGGCTGAGATAGGAGAATTGCTTGAACCCAGGA GTGGCACGAGCCTGTAACCCCAGCTACTTGGGCGGCTGAGATAGGAGAATTGCTTGAACCCAGGA T G SKA2 Ensembl:ENSG00000182628 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1468306767 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5402,RMVar_hsa_circ_341275 39895 RMVar_ID_39895 Human_SNP_ID_628743696 A-to-I Human chr17 - 59127566 59127560 59127566 CCTGGCTAACATGATGAAACCCGTCTCTACTAAAAATACAAAATTAGCCGGGCGTGGTGGCACGA CCTGGCTAACATGATGAAACCCGTCTCTACTA______CAAAATTAGCCGGGCGTGGTGGCACGA GTATTTT G SKA2 Ensembl:ENSG00000182628 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1236956238 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_25345101 RMVar_hsa_circ_5402,RMVar_hsa_circ_341275 39896 RMVar_ID_39896 Human_SNP_ID_628744050 A-to-I Human chr17 - 59129205 59129205 59129205 GCCTGGAACTATAGGCACACACCACCACACCCAGCTAATTTTTGTATTTTTAGTGGAGATGGGAT GCCTGGAACTATAGGCACACACCACCACACCCGGCTAATTTTTGTATTTTTAGTGGAGATGGGAT T C SKA2 Ensembl:ENSG00000182628 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1416723425 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5402,RMVar_hsa_circ_341275 39897 RMVar_ID_39897 Human_SNP_ID_628752318 A-to-I Human chr17 + 59164683 59164683 59164683 TGGCCGTACAGGACTTCAAGACCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATAA TGGCCGTACAGGACTTCAAGACCAGCCTGGCCGACATGGTGAAACCCCATCTCTACTAAAAATAA A G PRR11 Ensembl:ENSG00000068489 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917052009 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_317449 39898 RMVar_ID_39898 Human_SNP_ID_628755978 A-to-I Human chr17 + 59179197 59179197 59179197 AATTTTTGTATTTTTAGTAGAGATCAGATTTTACTATGTTGGTCAGGCTGGTCTCTAACTCCTGA AATTTTTGTATTTTTAGTAGAGATCAGATTTTGCTATGTTGGTCAGGCTGGTCTCTAACTCCTGA A G PRR11 Ensembl:ENSG00000068489 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1360989414 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_335578,RMVar_hsa_circ_185759 39899 RMVar_ID_39899 Human_SNP_ID_628758503 A-to-I Human chr17 + 59189137 59189135 59189137 CCTAGCCAACATGATGAAACCCCCTCTCTACTAAAAAACACAAAAATTAGCTGGGCGTGGTGGCG CCTAGCCAACATGATGAAACCCCCTCTCTAC__AAAAACACAAAAATTAGCTGGGCGTGGTGGCG CTA C PRR11 Ensembl:ENSG00000068489 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1491116233 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_335578,RMVar_hsa_circ_20751,RMVar_hsa_circ_185759,RMVar_hsa_circ_308963 39900 RMVar_ID_39900 Human_SNP_ID_628758504 A-to-I Human chr17 + 59189137 59189136 59189137 CCTAGCCAACATGATGAAACCCCCTCTCTACTAAAAAACACAAAAATTAGCTGGGCGTGGTGGCG CCTAGCCAACATGATGAAACCCCCTCTCTACT_AAAAACACAAAAATTAGCTGGGCGTGGTGGCG TA T PRR11 Ensembl:ENSG00000068489 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1163718547 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_335578,RMVar_hsa_circ_20751,RMVar_hsa_circ_185759,RMVar_hsa_circ_308963 39901 RMVar_ID_39901 Human_SNP_ID_628761413 A-to-I Human chr17 + 59201872 59201872 59201872 GGGTGCCTGTAATCCCAGCTATGCGGGAGGCTAAGGCAGGAGAATTGCTTGAACCCAAGAGGCAG GGGTGCCTGTAATCCCAGCTATGCGGGAGGCTGAGGCAGGAGAATTGCTTGAACCCAAGAGGCAG A G AC099850.3,PRR11 Ensembl:ENSG00000265303,Ensembl:ENSG00000068489 Protein coding,Protein coding intron,intron GSE47997;GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,29129909,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs1568329072 Functional Loss SNV dbSNP153 33..33 33 - - - 39902 RMVar_ID_39902 Human_SNP_ID_628761423 A-to-I Human chr17 + 59201920 59201920 59201920 TTGAACCCAAGAGGCAGAGGTTGCAGTGAGCCAAGATCGCGTCATTGCACTCCAGCCTGAGCAAC TTGAACCCAAGAGGCAGAGGTTGCAGTGAGCCGAGATCGCGTCATTGCACTCCAGCCTGAGCAAC A G AC099850.3,PRR11 Ensembl:ENSG00000265303,Ensembl:ENSG00000068489 Protein coding,Protein coding intron,intron GSE47997;GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,31158229,31158229,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs940084227 Functional Loss SNV dbSNP153 33..33 33 - - - 39903 RMVar_ID_39903 Human_SNP_ID_628761515 A-to-I Human chr17 + 59202354 59202354 59202354 AGGCCAAGGTGGGAGGATTGCTTGAGCCCAGGAATTCAAGACTAGCCTGGGCAACATAATACAGG AGGCCAAGGTGGGAGGATTGCTTGAGCCCAGGGATTCAAGACTAGCCTGGGCAACATAATACAGG A G AC099850.3,PRR11 Ensembl:ENSG00000265303,Ensembl:ENSG00000068489 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1355284853 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8458611 39904 RMVar_ID_39904 Human_SNP_ID_628761667 A-to-I Human chr17 + 59203198 59203198 59203198 GAGGCAGTCCTGTTTTTGAGACCCACATCTATATATAGAGATTTTTGTTTGTTTGTTTGTTTGTT GAGGCAGTCCTGTTTTTGAGACCCACATCTATGTATAGAGATTTTTGTTTGTTTGTTTGTTTGTT A G AC099850.3,PRR11 Ensembl:ENSG00000265303,Ensembl:ENSG00000068489 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1183631783 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6622898,Human_RBP_ID_8193091,Human_RBP_ID_22500055,Human_RBP_ID_23170957,Human_RBP_ID_26458069,Human_RBP_ID_27667782 39905 RMVar_ID_39905 Human_SNP_ID_628761691 A-to-I Human chr17 + 59203280 59203280 59203280 GAAGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGCGCAATCTTGGCTCACTGCAACCTCCAC GAAGTCTCACTCTGTCACCCAGGCTGGAGTGCGGTGGCGCAATCTTGGCTCACTGCAACCTCCAC A G AC099850.3,PRR11 Ensembl:ENSG00000265303,Ensembl:ENSG00000068489 Protein coding,Protein coding intron,intron GSE38233;GSE99789 cultured B-cells;esophageal squamous carcinoma cells,EC109 - 24183664,29796672 RNA-Seq:(High) rs573683802 Functional Loss SNV dbSNP153 33..33 33 - - - 39906 RMVar_ID_39906 Human_SNP_ID_628761701 A-to-I Human chr17 + 59203324 59203324 59203324 TTGGCTCACTGCAACCTCCACCTCCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGC TTGGCTCACTGCAACCTCCACCTCCCAGGTTCGAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGC A G AC099850.3,PRR11 Ensembl:ENSG00000265303,Ensembl:ENSG00000068489 Protein coding,Protein coding intron,intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1252159118 Functional Loss SNV dbSNP153 33..33 33 - - - 39907 RMVar_ID_39907 Human_SNP_ID_628761720 A-to-I Human chr17 + 59203380 59203380 59203380 CTGAGTAGCTGGGATTACAGGTGCGCACTGCCACGCCTGACTAATTTTTGTATTTCTAGTAAAGA CTGAGTAGCTGGGATTACAGGTGCGCACTGCCTCGCCTGACTAATTTTTGTATTTCTAGTAAAGA A T AC099850.3,PRR11 Ensembl:ENSG00000265303,Ensembl:ENSG00000068489 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1472179757 Functional Loss SNV dbSNP153 33..33 33 - - - 39908 RMVar_ID_39908 Human_SNP_ID_628761741 A-to-I Human chr17 + 59203486 59203486 59203486 ACCTCAGGTGATCCACCCATCTCAGCCTCCCAAAGTGCTGAGATTACAGGCGTGAGCCACCACGC ACCTCAGGTGATCCACCCATCTCAGCCTCCCAGAGTGCTGAGATTACAGGCGTGAGCCACCACGC A G AC099850.3,PRR11 Ensembl:ENSG00000265303,Ensembl:ENSG00000068489 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs999993720 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1847078,Human_Splice_Rec_1847098 39909 RMVar_ID_39909 Human_SNP_ID_628761792 A-to-I Human chr17 + 59203694 59203694 59203694 CAGCCTGGCCAACATGGTGAAATCCCATCTCTACTAAAAATACAAAATTAGCCAGGTGTGGTGTC CAGCCTGGCCAACATGGTGAAATCCCATCTCTGCTAAAAATACAAAATTAGCCAGGTGTGGTGTC A G AC099850.3,PRR11 Ensembl:ENSG00000265303,Ensembl:ENSG00000068489 Protein coding,Protein coding intron,3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs3206829 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1847036 39910 RMVar_ID_39910 Human_SNP_ID_628761794 A-to-I Human chr17 + 59203697 59203697 59203697 CCTGGCCAACATGGTGAAATCCCATCTCTACTAAAAATACAAAATTAGCCAGGTGTGGTGTCACG CCTGGCCAACATGGTGAAATCCCATCTCTACTGAAAATACAAAATTAGCCAGGTGTGGTGTCACG A G AC099850.3,PRR11 Ensembl:ENSG00000265303,Ensembl:ENSG00000068489 Protein coding,Protein coding intron,3'UTR GSE47997;GSE38233;GSE38233;GSE100210;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;cultured B-cells;cultured B-cells;HepG2 cell line;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,24183664,24183664,29129909,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs3206830 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1847036 39911 RMVar_ID_39911 Human_SNP_ID_628761795 A-to-I Human chr17 + 59203703 59203703 59203703 CAACATGGTGAAATCCCATCTCTACTAAAAATACAAAATTAGCCAGGTGTGGTGTCACGCACCTG CAACATGGTGAAATCCCATCTCTACTAAAAATCCAAAATTAGCCAGGTGTGGTGTCACGCACCTG A C AC099850.3,PRR11 Ensembl:ENSG00000265303,Ensembl:ENSG00000068489 Protein coding,Protein coding intron,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs12951618 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26453929 Human_Splice_Rec_1847036 39912 RMVar_ID_39912 Human_SNP_ID_628761796 A-to-I Human chr17 + 59203707 59203707 59203707 ATGGTGAAATCCCATCTCTACTAAAAATACAAAATTAGCCAGGTGTGGTGTCACGCACCTGTAGT ATGGTGAAATCCCATCTCTACTAAAAATACAATATTAGCCAGGTGTGGTGTCACGCACCTGTAGT A T AC099850.3,PRR11 Ensembl:ENSG00000265303,Ensembl:ENSG00000068489 Protein coding,Protein coding intron,3'UTR GSE47997;GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831 K562 cells&HepG2 cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line - 23474544,29129909,32596459 RNA-Seq:(High) rs907396222 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26453929 Human_Splice_Rec_1847036 39913 RMVar_ID_39913 Human_SNP_ID_628761797 A-to-I Human chr17 + 59203711 59203711 59203711 TGAAATCCCATCTCTACTAAAAATACAAAATTAGCCAGGTGTGGTGTCACGCACCTGTAGTCCCA TGAAATCCCATCTCTACTAAAAATACAAAATTCGCCAGGTGTGGTGTCACGCACCTGTAGTCCCA A C AC099850.3,PRR11 Ensembl:ENSG00000265303,Ensembl:ENSG00000068489 Protein coding,Protein coding intron,3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs12951628 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26453929 Human_Splice_Rec_1847036 39914 RMVar_ID_39914 Human_SNP_ID_628761798 A-to-I Human chr17 + 59203715 59203715 59203715 ATCCCATCTCTACTAAAAATACAAAATTAGCCAGGTGTGGTGTCACGCACCTGTAGTCCCAGTTA ATCCCATCTCTACTAAAAATACAAAATTAGCCGGGTGTGGTGTCACGCACCTGTAGTCCCAGTTA A G AC099850.3,PRR11 Ensembl:ENSG00000265303,Ensembl:ENSG00000068489 Protein coding,Protein coding intron,3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs3206831 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26453929 Human_Splice_Rec_1847036 39915 RMVar_ID_39915 Human_SNP_ID_628761806 A-to-I Human chr17 + 59203747 59203747 59203747 AGGTGTGGTGTCACGCACCTGTAGTCCCAGTTACTTGAACCTGGGAGGCAGAGGTTGCAGTGAGC AGGTGTGGTGTCACGCACCTGTAGTCCCAGTTTCTTGAACCTGGGAGGCAGAGGTTGCAGTGAGC A T AC099850.3,PRR11 Ensembl:ENSG00000265303,Ensembl:ENSG00000068489 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1292397153 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18294765,Human_RBP_ID_23308439,Human_RBP_ID_25307378,Human_RBP_ID_26459646 Human_miRNA_ID_697292,Human_miRNA_ID_702226,Human_miRNA_ID_1693860 39916 RMVar_ID_39916 Human_SNP_ID_628761811 A-to-I Human chr17 + 59203764 59203764 59203764 CCTGTAGTCCCAGTTACTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCCGAGATTGCAACACTGC CCTGTAGTCCCAGTTACTTGAACCTGGGAGGCGGAGGTTGCAGTGAGCCGAGATTGCAACACTGC A G AC099850.3,PRR11 Ensembl:ENSG00000265303,Ensembl:ENSG00000068489 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs3206832 Functional Loss SNV dbSNP153 33..33 33 - - - 39917 RMVar_ID_39917 Human_SNP_ID_628761907 A-to-I Human chr17 + 59204152 59204152 59204152 ACCATGGCTCACGCCTGTAATCCCAGGACTTTAGGAGGCCAAGGCAGGTGGATGACTTGAGCTCA ACCATGGCTCACGCCTGTAATCCCAGGACTTTCGGAGGCCAAGGCAGGTGGATGACTTGAGCTCA A C AC099850.3,PRR11 Ensembl:ENSG00000265303,Ensembl:ENSG00000068489 Protein coding,Protein coding intron,3'UTR GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29796672,31158229,32596459 RNA-Seq:(High) rs1178261626 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_697294,Human_miRNA_ID_702228 39918 RMVar_ID_39918 Human_SNP_ID_628761908 A-to-I Human chr17 + 59204152 59204152 59204152 ACCATGGCTCACGCCTGTAATCCCAGGACTTTAGGAGGCCAAGGCAGGTGGATGACTTGAGCTCA ACCATGGCTCACGCCTGTAATCCCAGGACTTTGGGAGGCCAAGGCAGGTGGATGACTTGAGCTCA A G AC099850.3,PRR11 Ensembl:ENSG00000265303,Ensembl:ENSG00000068489 Protein coding,Protein coding intron,3'UTR GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29796672,31158229,32596459 RNA-Seq:(High) rs1178261626 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_697294,Human_miRNA_ID_702228 39919 RMVar_ID_39919 Human_SNP_ID_628761911 A-to-I Human chr17 + 59204160 59204160 59204160 TCACGCCTGTAATCCCAGGACTTTAGGAGGCCAAGGCAGGTGGATGACTTGAGCTCAGGAGTTTG TCACGCCTGTAATCCCAGGACTTTAGGAGGCCGAGGCAGGTGGATGACTTGAGCTCAGGAGTTTG A G AC099850.3,PRR11 Ensembl:ENSG00000265303,Ensembl:ENSG00000068489 Protein coding,Protein coding intron,3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1432935162 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_697294,Human_miRNA_ID_702228 39920 RMVar_ID_39920 Human_SNP_ID_628761950 A-to-I Human chr17 + 59204328 59204328 59204328 TGAGGTGGGAGGATGGTTTGGGCCCCGGAGGTAGAGGTTGCAGTGAGCTGAGATTGTGCCACTGT TGAGGTGGGAGGATGGTTTGGGCCCCGGAGGTGGAGGTTGCAGTGAGCTGAGATTGTGCCACTGT A G AC099850.3,PRR11 Ensembl:ENSG00000265303,Ensembl:ENSG00000068489 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924441441 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_495796,Human_RBP_ID_6622906,Human_RBP_ID_8193093,Human_RBP_ID_17904447,Human_RBP_ID_26458072 39921 RMVar_ID_39921 Human_SNP_ID_628761990 A-to-I Human chr17 + 59204430 59204430 59204430 AAAAAAAAAAAAAAAAAAAAAAGGCCTGGCACAGTGGCTCACGCCTGTAATCCCAGCACTTTGGG AAAAAAAAAAAAAAAAAAAAAAGGCCTGGCACCGTGGCTCACGCCTGTAATCCCAGCACTTTGGG A C AC099850.3,PRR11 Ensembl:ENSG00000265303,Ensembl:ENSG00000068489 Protein coding,Protein coding intron,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1156732985 Functional Loss SNV dbSNP153 33..33 33 - - - 39922 RMVar_ID_39922 Human_SNP_ID_628762118 A-to-I Human chr17 + 59204907 59204907 59204907 AAAATTAGCCGGGAGCGGTGATGTGTGCCTGTAGTCCCAGCTACTCAGGAGACTGAGGTGGGAGA AAAATTAGCCGGGAGCGGTGATGTGTGCCTGTGGTCCCAGCTACTCAGGAGACTGAGGTGGGAGA A G AC099850.3,PRR11 Ensembl:ENSG00000265303,Ensembl:ENSG00000068489 Protein coding,Protein coding intron,3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1426706301 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_495802 39923 RMVar_ID_39923 Human_SNP_ID_628764786 A-to-I Human chr17 + 59214480 59214480 59214480 TTGCACAGGCTGGAGGGCAGTGGTGCAATCTCAGCTCACTGCACCTCCGCCTCCTGGGTTCAAGC TTGCACAGGCTGGAGGGCAGTGGTGCAATCTCGGCTCACTGCACCTCCGCCTCCTGGGTTCAAGC A G AC099850.3,SMG8 Ensembl:ENSG00000265303,Ensembl:ENSG00000167447 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1300621230 Functional Loss SNV dbSNP153 33..33 33 - - - 39924 RMVar_ID_39924 Human_SNP_ID_628764803 A-to-I Human chr17 + 59214547 59214547 59214547 TTCTCCTGCCCCAGCCTCCCCAGTAACAGATTACAGGCACACGCCACCACACCTGACTAATTTTT TTCTCCTGCCCCAGCCTCCCCAGTAACAGATTGCAGGCACACGCCACCACACCTGACTAATTTTT A G AC099850.3,SMG8 Ensembl:ENSG00000265303,Ensembl:ENSG00000167447 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1184956673 Functional Loss SNV dbSNP153 33..33 33 - - - 39925 RMVar_ID_39925 Human_SNP_ID_628779591 A-to-I Human chr17 + 59274095 59274095 59274095 TGATTAATAACATACACAGAAATGTACATACTACATCATCTACAGAAATCTTGATCAATAACCTA TGATTAATAACATACACAGAAATGTACATACTGCATCATCTACAGAAATCTTGATCAATAACCTA A G GDPD1 Ensembl:ENSG00000153982 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1357486064 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268896,RMVar_hsa_circ_185771 39926 RMVar_ID_39926 Human_SNP_ID_628779592 A-to-I Human chr17 + 59274095 59274095 59274095 TGATTAATAACATACACAGAAATGTACATACTACATCATCTACAGAAATCTTGATCAATAACCTA TGATTAATAACATACACAGAAATGTACATACTTCATCATCTACAGAAATCTTGATCAATAACCTA A T GDPD1 Ensembl:ENSG00000153982 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1357486064 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268896,RMVar_hsa_circ_185771 39927 RMVar_ID_39927 Human_SNP_ID_628779613 A-to-I Human chr17 + 59274148 59274148 59274148 ATCAATAACCTAGAAACTAGGTTATCTAGGTTATTGATCAAGATTTCTGTAGATGATGCAGTGTT ATCAATAACCTAGAAACTAGGTTATCTAGGTTTTTGATCAAGATTTCTGTAGATGATGCAGTGTT A T GDPD1 Ensembl:ENSG00000153982 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334626518 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18294783,Human_RBP_ID_24480151 RMVar_hsa_circ_268896,RMVar_hsa_circ_185771 39928 RMVar_ID_39928 Human_SNP_ID_628779639 A-to-I Human chr17 + 59274310 59274309 59274310 TGAGACAGGCGGATCATCTGAAGTCAGGAGTTAAAGACCAGCCTGGCCAACATGGCAAAACCCCA TGAGACAGGCGGATCATCTGAAGTCAGGAGTT_AAGACCAGCCTGGCCAACATGGCAAAACCCCA TA T GDPD1 Ensembl:ENSG00000153982 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs903413378 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_268896,RMVar_hsa_circ_185771 39929 RMVar_ID_39929 Human_SNP_ID_628779776 A-to-I Human chr17 + 59274657 59274657 59274657 AAAAATTAGCTGGGCGTGGTGGTGGGCACCTTAGTCCCAGCTACTCGGGAGGCTGAGTCAGGAGA AAAAATTAGCTGGGCGTGGTGGTGGGCACCTTTGTCCCAGCTACTCGGGAGGCTGAGTCAGGAGA A T GDPD1 Ensembl:ENSG00000153982 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1452096015 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268896,RMVar_hsa_circ_185771 39930 RMVar_ID_39930 Human_SNP_ID_628779893 A-to-I Human chr17 + 59274971 59274971 59274971 TCCAGCAATTCTCCTGCCTCTGCCTCCCGAGTACCTGGGATTACAGGTGCCTGCTACCATGCCCA TCCAGCAATTCTCCTGCCTCTGCCTCCCGAGTGCCTGGGATTACAGGTGCCTGCTACCATGCCCA A G GDPD1 Ensembl:ENSG00000153982 Protein coding 3'UTR GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1346795097 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268896,RMVar_hsa_circ_185771 39931 RMVar_ID_39931 Human_SNP_ID_628856510 A-to-I Human chr17 + 59587638 59587638 59587638 TGCCACCACACCCAGCTAATTTTTGTGTTTTTAGTGGAAACGGGGTTTTGCCATGTTGGCCAGGC TGCCACCACACCCAGCTAATTTTTGTGTTTTTGGTGGAAACGGGGTTTTGCCATGTTGGCCAGGC A G DHX40 Ensembl:ENSG00000108406 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs543100925 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_310180,RMVar_hsa_circ_11620,RMVar_hsa_circ_11391,RMVar_hsa_circ_361669,RMVar_hsa_circ_185784,RMVar_hsa_circ_114130,RMVar_hsa_circ_42717,RMVar_hsa_circ_185785,RMVar_hsa_circ_185786,RMVar_hsa_circ_339221,RMVar_hsa_circ_37343,RMVar_hsa_circ_8299,RMVar_hsa_circ_6988,RMVar_hsa_circ_357684,RMVar_hsa_circ_281192,RMVar_hsa_circ_348461,RMVar_hsa_circ_185788 39932 RMVar_ID_39932 Human_SNP_ID_628863408 A-to-I Human chr17 + 59616493 59616493 59616493 GGGAGGCTGAGGCAGGAGAATTGCCTGAACCCAGGAGGCGGAGGTTGTGGTGGGCCGAGATCACA GGGAGGCTGAGGCAGGAGAATTGCCTGAACCCGGGAGGCGGAGGTTGTGGTGGGCCGAGATCACA A G RF00017-1190 RNACentral:URS000092EF5C SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1424615331 Functional Loss SNV dbSNP153 33..33 33 - - - 39933 RMVar_ID_39933 Human_SNP_ID_628867699 A-to-I Human chr17 + 59633930 59633930 59633930 GTCAGCAATAAGTATTATATATATTTTTTGAGATGGGGTCTTGCTCTGTCACCCAGGCTGAAGTG GTCAGCAATAAGTATTATATATATTTTTTGAGGTGGGGTCTTGCTCTGTCACCCAGGCTGAAGTG A G CLTC Ensembl:ENSG00000141367 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1016552444 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17566063 39934 RMVar_ID_39934 Human_SNP_ID_628867719 A-to-I Human chr17 + 59634021 59634021 59634021 GCCTCTGCCTCCTGGACTCAAACAATCTTCCCACCTCAGCCTGCCAACTAGCTAGAACTACAGGT GCCTCTGCCTCCTGGACTCAAACAATCTTCCCCCCTCAGCCTGCCAACTAGCTAGAACTACAGGT A C CLTC Ensembl:ENSG00000141367 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs996785463 Functional Loss SNV dbSNP153 33..33 33 - - - 39935 RMVar_ID_39935 Human_SNP_ID_628867723 A-to-I Human chr17 + 59634042 59634042 59634042 ACAATCTTCCCACCTCAGCCTGCCAACTAGCTAGAACTACAGGTGCACACCACCACGCCTGGACA ACAATCTTCCCACCTCAGCCTGCCAACTAGCTGGAACTACAGGTGCACACCACCACGCCTGGACA A G CLTC Ensembl:ENSG00000141367 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs555683481 Functional Loss SNV dbSNP153 33..33 33 - - - 39936 RMVar_ID_39936 Human_SNP_ID_628868523 A-to-I Human chr17 + 59637591 59637591 59637591 AAAAAAAAAAAATTTTTTTTTTAGCCGGGTACAGTGACTCATGCCTGTAATCCCAGCACTTTGGG AAAAAAAAAAAATTTTTTTTTTAGCCGGGTACGGTGACTCATGCCTGTAATCCCAGCACTTTGGG A G CLTC Ensembl:ENSG00000141367 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285653587 Functional Loss SNV dbSNP153 33..33 33 - - - 39937 RMVar_ID_39937 Human_SNP_ID_628873193 A-to-I Human chr17 + 59657605 59657604 59657606 CCTGGCCAACATGGTGAAACCCTGTCTCTACTAAAAATACAAAAAGTTAGCCGGCTGTGGTGGTG CCTGGCCAACATGGTGAAACCCTGTCTCTACT__AAATACAAAAAGTTAGCCGGCTGTGGTGGTG TAA T CLTC Ensembl:ENSG00000141367 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1159517033 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_6356,RMVar_hsa_circ_363598,RMVar_hsa_circ_378026,RMVar_hsa_circ_69328,RMVar_hsa_circ_60509,RMVar_hsa_circ_105784,RMVar_hsa_circ_353262,RMVar_hsa_circ_67245,RMVar_hsa_circ_89013,RMVar_hsa_circ_24294,RMVar_hsa_circ_43106,RMVar_hsa_circ_17451,RMVar_hsa_circ_21798,RMVar_hsa_circ_60960,RMVar_hsa_circ_185794,RMVar_hsa_circ_185795,RMVar_hsa_circ_266388,RMVar_hsa_circ_351675,RMVar_hsa_circ_374301,RMVar_hsa_circ_71300,RMVar_hsa_circ_52794,RMVar_hsa_circ_185796,RMVar_hsa_circ_50730,RMVar_hsa_circ_295995,RMVar_hsa_circ_299581,RMVar_hsa_circ_361315,RMVar_hsa_circ_185798,RMVar_hsa_circ_24250,RMVar_hsa_circ_329777,RMVar_hsa_circ_185797,RMVar_hsa_circ_302207,RMVar_hsa_circ_185799 39938 RMVar_ID_39938 Human_SNP_ID_628873194 A-to-I Human chr17 + 59657605 59657605 59657605 CCTGGCCAACATGGTGAAACCCTGTCTCTACTAAAAATACAAAAAGTTAGCCGGCTGTGGTGGTG CCTGGCCAACATGGTGAAACCCTGTCTCTACTGAAAATACAAAAAGTTAGCCGGCTGTGGTGGTG A G CLTC Ensembl:ENSG00000141367 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1367436544 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6356,RMVar_hsa_circ_363598,RMVar_hsa_circ_378026,RMVar_hsa_circ_69328,RMVar_hsa_circ_60509,RMVar_hsa_circ_105784,RMVar_hsa_circ_353262,RMVar_hsa_circ_67245,RMVar_hsa_circ_89013,RMVar_hsa_circ_24294,RMVar_hsa_circ_43106,RMVar_hsa_circ_17451,RMVar_hsa_circ_21798,RMVar_hsa_circ_60960,RMVar_hsa_circ_185794,RMVar_hsa_circ_185795,RMVar_hsa_circ_266388,RMVar_hsa_circ_351675,RMVar_hsa_circ_374301,RMVar_hsa_circ_71300,RMVar_hsa_circ_52794,RMVar_hsa_circ_185796,RMVar_hsa_circ_50730,RMVar_hsa_circ_295995,RMVar_hsa_circ_299581,RMVar_hsa_circ_361315,RMVar_hsa_circ_185798,RMVar_hsa_circ_24250,RMVar_hsa_circ_329777,RMVar_hsa_circ_185797,RMVar_hsa_circ_302207,RMVar_hsa_circ_185799 39939 RMVar_ID_39939 Human_SNP_ID_628879281 A-to-I Human chr17 + 59685597 59685597 59685597 CTTTCACTATTTCTTTGAATAGGATGCAATGCAGTATGCTTCTGAATCTAAAGATACTGAATTGG CTTTCACTATTTCTTTGAATAGGATGCAATGCGGTATGCTTCTGAATCTAAAGATACTGAATTGG A G CLTC Ensembl:ENSG00000141367 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1378922042 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1009695,Human_RBP_ID_8090877,Human_RBP_ID_8820666,Human_RBP_ID_9287940,Human_RBP_ID_9340995,Human_RBP_ID_23739736,Human_RBP_ID_27667954 Human_Splice_Rec_1847508,Human_Splice_Rec_1847570,Human_Splice_Rec_1847630,Human_Splice_Rec_1847658,Human_Splice_Rec_1847700,Human_Splice_Rec_1847708 Human_miRNA_ID_3103954 RMVar_hsa_circ_89013,RMVar_hsa_circ_185795,RMVar_hsa_circ_5046,RMVar_hsa_circ_1340,RMVar_hsa_circ_103547,RMVar_hsa_circ_185807,RMVar_hsa_circ_114198,RMVar_hsa_circ_62282,RMVar_hsa_circ_64865,RMVar_hsa_circ_185811,RMVar_hsa_circ_66011,RMVar_hsa_circ_21206,RMVar_hsa_circ_15954,RMVar_hsa_circ_185815,RMVar_hsa_circ_89432,RMVar_hsa_circ_336285,RMVar_hsa_circ_368688,RMVar_hsa_circ_96798,RMVar_hsa_circ_185818,RMVar_hsa_circ_38891 39940 RMVar_ID_39940 Human_SNP_ID_628880897 A-to-I Human chr17 + 59692776 59692776 59692776 CTCCTGCCTCAACCTGCTGAGTAGCTGGGATTATAAGCATGCACCACCACGCCCGGCTAATTTTT CTCCTGCCTCAACCTGCTGAGTAGCTGGGATTGTAAGCATGCACCACCACGCCCGGCTAATTTTT A G CLTC Ensembl:ENSG00000141367 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1440035958 Functional Loss SNV dbSNP153 33..33 33 - - - 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 39941 RMVar_ID_39941 Human_SNP_ID_628880942 A-to-I Human chr17 + 59692914 59692914 59692914 CCCTCCTCGGCCTCCCACGGTGCTGGGATTACAGGCGTGAGCCACCGCGCCCGGCCCAAATGTGT CCCTCCTCGGCCTCCCACGGTGCTGGGATTACGGGCGTGAGCCACCGCGCCCGGCCCAAATGTGT A G CLTC Ensembl:ENSG00000141367 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs553840601 Functional Loss SNV dbSNP153 33..33 33 - - - 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 39942 RMVar_ID_39942 Human_SNP_ID_628881021 A-to-I Human chr17 + 59693244 59693244 59693244 CAAAAATTAGCTGGACATGGTGGCGCACACCCATAATCCCAGCTACTCGGGAGGCTGAGGCACGA CAAAAATTAGCTGGACATGGTGGCGCACACCCGTAATCCCAGCTACTCGGGAGGCTGAGGCACGA A G CLTC Ensembl:ENSG00000141367 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs896757267 Functional Loss SNV dbSNP153 33..33 33 - - - 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 39943 RMVar_ID_39943 Human_SNP_ID_628881029 A-to-I Human chr17 + 59693278 59693277 59693278 AATCCCAGCTACTCGGGAGGCTGAGGCACGAGAATCACTTGAACCCAGGAGGCAGAGGTTTCAGT AATCCCAGCTACTCGGGAGGCTGAGGCACGAG_ATCACTTGAACCCAGGAGGCAGAGGTTTCAGT GA G CLTC Ensembl:ENSG00000141367 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs796549027 Functional Loss DEL dbSNP153 33..33 33 - - - 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 39944 RMVar_ID_39944 Human_SNP_ID_628881030 A-to-I Human chr17 + 59693292 59693292 59693292 GGGAGGCTGAGGCACGAGAATCACTTGAACCCAGGAGGCAGAGGTTTCAGTGAGCCGAGATTACA GGGAGGCTGAGGCACGAGAATCACTTGAACCCGGGAGGCAGAGGTTTCAGTGAGCCGAGATTACA A G CLTC Ensembl:ENSG00000141367 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs531919420 Functional Loss SNV dbSNP153 33..33 33 - - - 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 39945 RMVar_ID_39945 Human_SNP_ID_628882458 A-to-I Human chr17 - 59698836 59698832 59698837 GAGTACCCATACAACCATTGTTTTCCACTTACAGTATTCAATAAATTACAGGAGATATTCAACAC GAGTACCCATACAACCATTGTTTTCCACTTA_____TTCAATAAATTACAGGAGATATTCAACAC ATACTG A PTRH2 Ensembl:ENSG00000141378 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1283737757 Functional Loss DEL dbSNP153 32..36 33 - - - Human_RBP_ID_3531214,Human_RBP_ID_19083389 Human_miRNA_ID_2188501,Human_miRNA_ID_2190873,Human_miRNA_ID_2605635 RMVar_hsa_circ_104429,RMVar_hsa_circ_108115,RMVar_hsa_circ_185821,RMVar_hsa_circ_185822 39946 RMVar_ID_39946 Human_SNP_ID_628882459 A-to-I Human chr17 - 59698836 59698836 59698836 GAGTACCCATACAACCATTGTTTTCCACTTACAGTATTCAATAAATTACAGGAGATATTCAACAC GAGTACCCATACAACCATTGTTTTCCACTTACGGTATTCAATAAATTACAGGAGATATTCAACAC T C PTRH2 Ensembl:ENSG00000141378 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1335536611 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3531214,Human_RBP_ID_19083389 Human_miRNA_ID_2188501,Human_miRNA_ID_2190873,Human_miRNA_ID_2605635 RMVar_hsa_circ_104429,RMVar_hsa_circ_108115,RMVar_hsa_circ_185821,RMVar_hsa_circ_185822 39947 RMVar_ID_39947 Human_SNP_ID_628882466 A-to-I Human chr17 - 59698858 59698855 59698859 TTCAGCTGTGTAAATTAATGGTGAGTACCCATACAACCATTGTTTTCCACTTACAGTATTCAATA TTCAGCTGTGTAAATTAATGGTGAGTACCCA____ACCATTGTTTTCCACTTACAGTATTCAATA TTGTA T PTRH2 Ensembl:ENSG00000141378 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1233103820 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_19083389 RMVar_hsa_circ_104429,RMVar_hsa_circ_108115,RMVar_hsa_circ_185821,RMVar_hsa_circ_185822 39948 RMVar_ID_39948 Human_SNP_ID_628884056 A-to-I Human chr17 - 59705799 59705799 59705799 CCTGAGGTGTCCTCCTACCTTATCCCCTGAGTAGCTGGGAGTATGGGCATGTGGCACCACATCTG CCTGAGGTGTCCTCCTACCTTATCCCCTGAGTGGCTGGGAGTATGGGCATGTGGCACCACATCTG T C PTRH2 Ensembl:ENSG00000141378 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs527314064 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17566068 RMVar_hsa_circ_108115,RMVar_hsa_circ_185822 39949 RMVar_ID_39949 Human_SNP_ID_628886720 A-to-I Human chr17 + 59717476 59717476 59717476 ACTGTCTAGGCCCACTGCAACCTCCACCTCCCAGGCTCAAGCGATTCTTGTGCCTCAGCCTCCCA ACTGTCTAGGCCCACTGCAACCTCCACCTCCCGGGCTCAAGCGATTCTTGTGCCTCAGCCTCCCA A G VMP1 Ensembl:ENSG00000062716 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1209197514 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_185824,RMVar_hsa_circ_107652,RMVar_hsa_circ_111770,RMVar_hsa_circ_102889,RMVar_hsa_circ_185825,RMVar_hsa_circ_185823 39950 RMVar_ID_39950 Human_SNP_ID_628911074 A-to-I Human chr17 + 59822965 59822965 59822965 CAAATTAGTTGGGCATGGTGGTACCCGCCTGTAGTCCCTGCTACCCAAGAGGCTGAGATGGAAAA CAAATTAGTTGGGCATGGTGGTACCCGCCTGTGGTCCCTGCTACCCAAGAGGCTGAGATGGAAAA A G VMP1 Ensembl:ENSG00000062716 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs570388627 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13105462 RMVar_hsa_circ_102889,RMVar_hsa_circ_185825,RMVar_hsa_circ_87762,RMVar_hsa_circ_185835,RMVar_hsa_circ_185844,RMVar_hsa_circ_336973,RMVar_hsa_circ_79913,RMVar_hsa_circ_79474,RMVar_hsa_circ_88941,RMVar_hsa_circ_185853,RMVar_hsa_circ_185854,RMVar_hsa_circ_120271,RMVar_hsa_circ_185860,RMVar_hsa_circ_92862,RMVar_hsa_circ_185859 39951 RMVar_ID_39951 Human_SNP_ID_628911751 A-to-I Human chr17 + 59825263 59825263 59825263 GCCTGGCTAATTTTTGTGTCTTTAGTAGAGACAGGATTTCACGATGTTGGCTAGGCTGGTCTCAA GCCTGGCTAATTTTTGTGTCTTTAGTAGAGACGGGATTTCACGATGTTGGCTAGGCTGGTCTCAA A G VMP1 Ensembl:ENSG00000062716 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs953305957 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102889,RMVar_hsa_circ_185825,RMVar_hsa_circ_87762,RMVar_hsa_circ_185835,RMVar_hsa_circ_185844,RMVar_hsa_circ_336973,RMVar_hsa_circ_79913,RMVar_hsa_circ_79474,RMVar_hsa_circ_88941,RMVar_hsa_circ_185853,RMVar_hsa_circ_185854,RMVar_hsa_circ_120271,RMVar_hsa_circ_185860,RMVar_hsa_circ_92862,RMVar_hsa_circ_185859 39952 RMVar_ID_39952 Human_SNP_ID_628912179 A-to-I Human chr17 + 59827462 59827462 59827462 CCTCAGCCTCCCAAGCAGCTAAGACTACAGGCATGCACCACCACCCCCAGCTAATTTTTGTATTT CCTCAGCCTCCCAAGCAGCTAAGACTACAGGCGTGCACCACCACCCCCAGCTAATTTTTGTATTT A G VMP1 Ensembl:ENSG00000062716 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2526352 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102889,RMVar_hsa_circ_185825,RMVar_hsa_circ_87762,RMVar_hsa_circ_185835,RMVar_hsa_circ_185844,RMVar_hsa_circ_336973,RMVar_hsa_circ_79913,RMVar_hsa_circ_79474,RMVar_hsa_circ_88941,RMVar_hsa_circ_185853,RMVar_hsa_circ_185854,RMVar_hsa_circ_120271,RMVar_hsa_circ_185860,RMVar_hsa_circ_92862,RMVar_hsa_circ_185859 39953 RMVar_ID_39953 Human_SNP_ID_628912180 A-to-I Human chr17 + 59827462 59827462 59827462 CCTCAGCCTCCCAAGCAGCTAAGACTACAGGCATGCACCACCACCCCCAGCTAATTTTTGTATTT CCTCAGCCTCCCAAGCAGCTAAGACTACAGGCTTGCACCACCACCCCCAGCTAATTTTTGTATTT A T VMP1 Ensembl:ENSG00000062716 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2526352 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102889,RMVar_hsa_circ_185825,RMVar_hsa_circ_87762,RMVar_hsa_circ_185835,RMVar_hsa_circ_185844,RMVar_hsa_circ_336973,RMVar_hsa_circ_79913,RMVar_hsa_circ_79474,RMVar_hsa_circ_88941,RMVar_hsa_circ_185853,RMVar_hsa_circ_185854,RMVar_hsa_circ_120271,RMVar_hsa_circ_185860,RMVar_hsa_circ_92862,RMVar_hsa_circ_185859 39954 RMVar_ID_39954 Human_SNP_ID_628915422 A-to-I Human chr17 - 59841778 59841778 59841778 AATTCGTATTTGCTTTCCTCTTTCCTTTCTTCAGACAAACACCAAATAAAATGCAGGTGAAAGAG AATTCGTATTTGCTTTCCTCTTTCCTTTCTTCTGACAAACACCAAATAAAATGCAGGTGAAAGAG T A - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs955929117 Functional Loss SNV dbSNP153 33..33 33 - - - 39955 RMVar_ID_39955 Human_SNP_ID_628925076 A-to-I Human chr17 - 59878561 59878561 59878561 ACAAGAATCTCGAACCGGGAGGCCGAGGTTGCAGTGAGCAGAGATGGTGCCACTGTACTCCAGCC ACAAGAATCTCGAACCGGGAGGCCGAGGTTGCGGTGAGCAGAGATGGTGCCACTGTACTCCAGCC T C TUBD1 Ensembl:ENSG00000108423 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1013147866 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_361005,RMVar_hsa_circ_361795,RMVar_hsa_circ_23722,RMVar_hsa_circ_103559,RMVar_hsa_circ_185867,RMVar_hsa_circ_62707,RMVar_hsa_circ_281675,RMVar_hsa_circ_306971,RMVar_hsa_circ_185874,RMVar_hsa_circ_185871,RMVar_hsa_circ_185869,RMVar_hsa_circ_355203,RMVar_hsa_circ_375480,RMVar_hsa_circ_323486,RMVar_hsa_circ_299544,RMVar_hsa_circ_331863,RMVar_hsa_circ_185870,RMVar_hsa_circ_330453,RMVar_hsa_circ_185875,RMVar_hsa_circ_185873 39956 RMVar_ID_39956 Human_SNP_ID_628925355 A-to-I Human chr17 - 59879498 59879498 59879498 CTGTGAAGCAGAGGTTGCATTGAGCCTAGATCATGTCACTGTACTCCAGCCTGGGCCACAGAGCA CTGTGAAGCAGAGGTTGCATTGAGCCTAGATCGTGTCACTGTACTCCAGCCTGGGCCACAGAGCA T C TUBD1 Ensembl:ENSG00000108423 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1454145118 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25308631 RMVar_hsa_circ_361005,RMVar_hsa_circ_361795,RMVar_hsa_circ_23722,RMVar_hsa_circ_103559,RMVar_hsa_circ_185867,RMVar_hsa_circ_62707,RMVar_hsa_circ_281675,RMVar_hsa_circ_306971,RMVar_hsa_circ_185874,RMVar_hsa_circ_185871,RMVar_hsa_circ_185869,RMVar_hsa_circ_355203,RMVar_hsa_circ_375480,RMVar_hsa_circ_323486,RMVar_hsa_circ_299544,RMVar_hsa_circ_331863,RMVar_hsa_circ_185870,RMVar_hsa_circ_330453,RMVar_hsa_circ_185875,RMVar_hsa_circ_185873 39957 RMVar_ID_39957 Human_SNP_ID_628926565 A-to-I Human chr17 - 59884050 59884050 59884050 CCCTATGTTGGCCAGGCTGCTCTCAAACTCCTAACTTCAAATGATCCACCCACCTCCGCCTCCCA CCCTATGTTGGCCAGGCTGCTCTCAAACTCCTGACTTCAAATGATCCACCCACCTCCGCCTCCCA T C TUBD1 Ensembl:ENSG00000108423 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1255696153 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_361005,RMVar_hsa_circ_23722,RMVar_hsa_circ_103559,RMVar_hsa_circ_185867,RMVar_hsa_circ_306971,RMVar_hsa_circ_185874,RMVar_hsa_circ_185871,RMVar_hsa_circ_375480,RMVar_hsa_circ_323486,RMVar_hsa_circ_299544,RMVar_hsa_circ_331863,RMVar_hsa_circ_185870,RMVar_hsa_circ_185875,RMVar_hsa_circ_313141 39958 RMVar_ID_39958 Human_SNP_ID_628926566 A-to-I Human chr17 - 59884058 59884058 59884058 CTGGATTTCCCTATGTTGGCCAGGCTGCTCTCAAACTCCTAACTTCAAATGATCCACCCACCTCC CTGGATTTCCCTATGTTGGCCAGGCTGCTCTCGAACTCCTAACTTCAAATGATCCACCCACCTCC T C TUBD1 Ensembl:ENSG00000108423 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913033197 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_361005,RMVar_hsa_circ_23722,RMVar_hsa_circ_103559,RMVar_hsa_circ_185867,RMVar_hsa_circ_306971,RMVar_hsa_circ_185874,RMVar_hsa_circ_185871,RMVar_hsa_circ_375480,RMVar_hsa_circ_323486,RMVar_hsa_circ_299544,RMVar_hsa_circ_331863,RMVar_hsa_circ_185870,RMVar_hsa_circ_185875,RMVar_hsa_circ_313141 39959 RMVar_ID_39959 Human_SNP_ID_628926777 A-to-I Human chr17 - 59884755 59884755 59884755 CTATGCCCAGCTAATTTTTGTATTTTTTTAGTAGAGACAAGGATTCAGCATGTTACCCAGACTGG CTATGCCCAGCTAATTTTTGTATTTTTTTAGTGGAGACAAGGATTCAGCATGTTACCCAGACTGG T C TUBD1 Ensembl:ENSG00000108423 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1346779569 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13106260 Human_Splice_Rec_1847950,Human_Splice_Rec_1847951 RMVar_hsa_circ_361005,RMVar_hsa_circ_23722,RMVar_hsa_circ_103559,RMVar_hsa_circ_185867,RMVar_hsa_circ_306971,RMVar_hsa_circ_185874,RMVar_hsa_circ_185871,RMVar_hsa_circ_375480,RMVar_hsa_circ_323486,RMVar_hsa_circ_299544,RMVar_hsa_circ_331863,RMVar_hsa_circ_185870,RMVar_hsa_circ_185875,RMVar_hsa_circ_313141 39960 RMVar_ID_39960 Human_SNP_ID_628928092 A-to-I Human chr17 - 59889547 59889547 59889547 CTCCTGCCTCAGCCTCATGAGTAGCTGGGACTACAGGCATGCGCCACCACGCCCAACTAATTTTT CTCCTGCCTCAGCCTCATGAGTAGCTGGGACTGCAGGCATGCGCCACCACGCCCAACTAATTTTT T C TUBD1 Ensembl:ENSG00000108423 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1278884535 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_361005,RMVar_hsa_circ_103559,RMVar_hsa_circ_185867,RMVar_hsa_circ_306971,RMVar_hsa_circ_323486,RMVar_hsa_circ_299544,RMVar_hsa_circ_185870,RMVar_hsa_circ_185875,RMVar_hsa_circ_313141,RMVar_hsa_circ_269075,RMVar_hsa_circ_336259 39961 RMVar_ID_39961 Human_SNP_ID_628929570 A-to-I Human chr17 + 59894730 59894730 59894730 GGGTTTAAGCGATTGTCATGGCTCAGCCTCCCAAGTAGCTAGGATTACAGGCATGCGCCACCACA GGGTTTAAGCGATTGTCATGGCTCAGCCTCCCGAGTAGCTAGGATTACAGGCATGCGCCACCACA A G RPS6KB1 Ensembl:ENSG00000108443 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs936340475 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113670,RMVar_hsa_circ_185876 39962 RMVar_ID_39962 Human_SNP_ID_628931807 A-to-I Human chr17 + 59902680 59902665 59902681 CTCGCTGCAGCTTCACCCTCCTGGGCTGAAGTAATTCTTCTGCCTCAGTCTCTCATGTAGCTGGG CTCGCTGCAGCTTCACCC________________TTCTTCTGCCTCAGTCTCTCATGTAGCTGGG CTCCTGGGCTGAAGTAA C RPS6KB1 Ensembl:ENSG00000108443 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1163602066 Functional Loss DEL dbSNP153 19..34 33 - - - Human_RBP_ID_3531448 RMVar_hsa_circ_113670,RMVar_hsa_circ_185876 39963 RMVar_ID_39963 Human_SNP_ID_628932511 A-to-I Human chr17 + 59905130 59905130 59905130 CCTTGACCTCTTGGACTCAAAGCAATCCTCCTACCTCATCCTCCTGAGTAGCTGGGACTGCAGAT CCTTGACCTCTTGGACTCAAAGCAATCCTCCTTCCTCATCCTCCTGAGTAGCTGGGACTGCAGAT A T RPS6KB1 Ensembl:ENSG00000108443 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1286996355 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13106697 RMVar_hsa_circ_113670,RMVar_hsa_circ_185876 39964 RMVar_ID_39964 Human_SNP_ID_628933593 A-to-I Human chr17 + 59909100 59909100 59909100 AGGCATGGGCCACCACGGCCGACTAATTTTGTATTTTTTTAGTAGAGATGGGGTTTCTCCATATT AGGCATGGGCCACCACGGCCGACTAATTTTGTGTTTTTTTAGTAGAGATGGGGTTTCTCCATATT A G RPS6KB1 Ensembl:ENSG00000108443 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1344393817 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113670,RMVar_hsa_circ_185876 39965 RMVar_ID_39965 Human_SNP_ID_628936264 A-to-I Human chr17 + 59919412 59919412 59919412 GGGAGGTGGAGGTTGCAGTGAGCCAAGATTGCACCATTGTGCTCTAGCTTGGACAACAAGAGCGA GGGAGGTGGAGGTTGCAGTGAGCCAAGATTGCCCCATTGTGCTCTAGCTTGGACAACAAGAGCGA A C RPS6KB1 Ensembl:ENSG00000108443 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1004729828 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1021,RMVar_hsa_circ_113670,RMVar_hsa_circ_300684,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_70228,RMVar_hsa_circ_185878,RMVar_hsa_circ_185879,RMVar_hsa_circ_185877,RMVar_hsa_circ_78766,RMVar_hsa_circ_114385,RMVar_hsa_circ_185881,RMVar_hsa_circ_185882 39966 RMVar_ID_39966 Human_SNP_ID_628936265 A-to-I Human chr17 + 59919412 59919412 59919412 GGGAGGTGGAGGTTGCAGTGAGCCAAGATTGCACCATTGTGCTCTAGCTTGGACAACAAGAGCGA GGGAGGTGGAGGTTGCAGTGAGCCAAGATTGCGCCATTGTGCTCTAGCTTGGACAACAAGAGCGA A G RPS6KB1 Ensembl:ENSG00000108443 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1004729828 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1021,RMVar_hsa_circ_113670,RMVar_hsa_circ_300684,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_70228,RMVar_hsa_circ_185878,RMVar_hsa_circ_185879,RMVar_hsa_circ_185877,RMVar_hsa_circ_78766,RMVar_hsa_circ_114385,RMVar_hsa_circ_185881,RMVar_hsa_circ_185882 39967 RMVar_ID_39967 Human_SNP_ID_628939282 A-to-I Human chr17 + 59932645 59932645 59932645 ATGATTACAGCTCACTGCAACCTCCGCCTCCCAGGCTCAAGTGATCCTTCCACCCCGGCCCCTCA ATGATTACAGCTCACTGCAACCTCCGCCTCCCGGGCTCAAGTGATCCTTCCACCCCGGCCCCTCA A G RPS6KB1 Ensembl:ENSG00000108443 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1205027803 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17566078 RMVar_hsa_circ_300684,RMVar_hsa_circ_356278,RMVar_hsa_circ_365799,RMVar_hsa_circ_335146,RMVar_hsa_circ_301385,RMVar_hsa_circ_185878,RMVar_hsa_circ_185877,RMVar_hsa_circ_84430,RMVar_hsa_circ_78766,RMVar_hsa_circ_114385,RMVar_hsa_circ_185881,RMVar_hsa_circ_185882,RMVar_hsa_circ_333376,RMVar_hsa_circ_365608,RMVar_hsa_circ_94126,RMVar_hsa_circ_185883,RMVar_hsa_circ_366359,RMVar_hsa_circ_185884 39968 RMVar_ID_39968 Human_SNP_ID_628945544 A-to-I Human chr17 - 59960566 59960566 59960566 CCTCAAGCGATCCGCCGACCTTGGCCTCCCAAAGTGCTGGGATTACAAGTGTGAGCCACTGCCCC CCTCAAGCGATCCGCCGACCTTGGCCTCCCAATGTGCTGGGATTACAAGTGTGAGCCACTGCCCC T A RNFT1 Ensembl:ENSG00000189050 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348120740 Functional Loss SNV dbSNP153 33..33 33 - - - 39969 RMVar_ID_39969 Human_SNP_ID_115017834 A-to-I Human chr2 - 225000893 225000893 225000893 CGGCTCACTGCAACCTCTGCGTCCTCAGTTCAAGCGATCCTCCTGCCTCAGCCTCCCGAGTAGCT CGGCTCACTGCAACCTCTGCGTCCTCAGTTCAGGCGATCCTCCTGCCTCAGCCTCCCGAGTAGCT T C DOCK10 Ensembl:ENSG00000135905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1344664926 Functional Loss SNV dbSNP153 33..33 33 - - - 39970 RMVar_ID_39970 Human_SNP_ID_115019275 A-to-I Human chr2 - 225007337 225007337 225007337 ATGGACTATTTACAGGTTTTATTTATGCATGCATCTAATTTAACAAAGTCAAGAGAGAGTTGTAA ATGGACTATTTACAGGTTTTATTTATGCATGCGTCTAATTTAACAAAGTCAAGAGAGAGTTGTAA T C DOCK10 Ensembl:ENSG00000135905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs573282848 Functional Loss SNV dbSNP153 33..33 33 - - - 39971 RMVar_ID_39971 Human_SNP_ID_115519650 A-to-I Human chr2 - 227021027 227021027 227021027 CCTTGTCTCTTACTAAAAGTACAAAAATTAGCAGGGCTTGGTGGCGGGCACCTGTAATCCCAGCC CCTTGTCTCTTACTAAAAGTACAAAAATTAGCCGGGCTTGGTGGCGGGCACCTGTAATCCCAGCC T G COL4A4 Ensembl:ENSG00000081052 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1367412847 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268870 39972 RMVar_ID_39972 Human_SNP_ID_115520168 A-to-I Human chr2 - 227022976 227022976 227022976 AATTATAGCTTTCCAACTGTGCTTTCAGCCCTAATGGACACTGGAATCATCGTGGGAGTTAAACA AATTATAGCTTTCCAACTGTGCTTTCAGCCCTTATGGACACTGGAATCATCGTGGGAGTTAAACA T A COL4A4 Ensembl:ENSG00000081052 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1376874418 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268870,RMVar_hsa_circ_23174 39973 RMVar_ID_39973 Human_SNP_ID_115524457 A-to-I Human chr2 - 227040732 227040731 227040733 TGGTGAAACGCCATCTCTACTAAAAATATAAAAGTTAGCTCTGTGGTGGTGCATGCCTGTAATCC TGGTGAAACGCCATCTCTACTAAAAATATAA__GTTAGCTCTGTGGTGGTGCATGCCTGTAATCC CTT C COL4A4 Ensembl:ENSG00000081052 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1352289513 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_23174 39974 RMVar_ID_39974 Human_SNP_ID_115584531 A-to-I Human chr2 + 227273663 227273662 227273663 TCCTACTCCCAACCCCAAACAATCCTTGCTTCAGCCTCCCAAAGTGCTAGGATTACAGGCGTGAG TCCTACTCCCAACCCCAAACAATCCTTGCTTC_GCCTCCCAAAGTGCTAGGATTACAGGCGTGAG CA C COL4A3 Ensembl:ENSG00000169031 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1185993149 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_268715,RMVar_hsa_circ_269681,RMVar_hsa_circ_267324 39975 RMVar_ID_39975 Human_SNP_ID_115584532 A-to-I Human chr2 + 227273663 227273663 227273663 TCCTACTCCCAACCCCAAACAATCCTTGCTTCAGCCTCCCAAAGTGCTAGGATTACAGGCGTGAG TCCTACTCCCAACCCCAAACAATCCTTGCTTCGGCCTCCCAAAGTGCTAGGATTACAGGCGTGAG A G COL4A3 Ensembl:ENSG00000169031 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1197443970 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268715,RMVar_hsa_circ_269681,RMVar_hsa_circ_267324 39976 RMVar_ID_39976 Human_SNP_ID_115584655 A-to-I Human chr2 + 227274219 227274219 227274219 AGATCGTGCTACTGCACTCCAGCCTGGGCAACAGATTGAGATACTGTCTCAAAAATAAATAAATA AGATCGTGCTACTGCACTCCAGCCTGGGCAACGGATTGAGATACTGTCTCAAAAATAAATAAATA A G COL4A3 Ensembl:ENSG00000169031 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1343624610 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268715,RMVar_hsa_circ_269681,RMVar_hsa_circ_267324 39977 RMVar_ID_39977 Human_SNP_ID_115584935 A-to-I Human chr2 - 227275243 227275243 227275243 CCAGGAGGTATAGGTTGCAGTGAGCCGAGATCACGCCACTGCACTGCAGCCTGGGTGGCAGAGCA CCAGGAGGTATAGGTTGCAGTGAGCCGAGATCCCGCCACTGCACTGCAGCCTGGGTGGCAGAGCA T G MFF-DT Ensembl:ENSG00000236432 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1218166863 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_207321 39978 RMVar_ID_39978 Human_SNP_ID_115605734 A-to-I Human chr2 + 227358143 227358143 227358143 CTCTGTTGCTGATGCTGGAGTCCCGTGGCATGATCTCAGCTCACTGCAACCTCCACCTCCCAGGT CTCTGTTGCTGATGCTGGAGTCCCGTGGCATGTTCTCAGCTCACTGCAACCTCCACCTCCCAGGT A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1280963639 Functional Loss SNV dbSNP153 33..33 33 - - - 39979 RMVar_ID_39979 Human_SNP_ID_115605741 A-to-I Human chr2 + 227358172 227358172 227358172 ATGATCTCAGCTCACTGCAACCTCCACCTCCCAGGTTCAAGTGATCCTTCTGCCTCAGCCTCCAG ATGATCTCAGCTCACTGCAACCTCCACCTCCCGGGTTCAAGTGATCCTTCTGCCTCAGCCTCCAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1254227729 Functional Loss SNV dbSNP153 33..33 33 - - - 39980 RMVar_ID_39980 Human_SNP_ID_115652519 A-to-I Human chr2 + 227540045 227540045 227540045 TTTAGTAGAGATGGGGTTTTGCCATGTTGACCAGACTGGTCTTGAACTCCTGGCCTCAAATGATC TTTAGTAGAGATGGGGTTTTGCCATGTTGACCCGACTGGTCTTGAACTCCTGGCCTCAAATGATC A C AGFG1 Ensembl:ENSG00000173744 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1210913981 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_207336,RMVar_hsa_circ_106504,RMVar_hsa_circ_367920,RMVar_hsa_circ_333137,RMVar_hsa_circ_207338,RMVar_hsa_circ_84527,RMVar_hsa_circ_33533,RMVar_hsa_circ_207352,RMVar_hsa_circ_18512,RMVar_hsa_circ_303193,RMVar_hsa_circ_207356,RMVar_hsa_circ_207360,RMVar_hsa_circ_11602,RMVar_hsa_circ_73766,RMVar_hsa_circ_4702,RMVar_hsa_circ_207363,RMVar_hsa_circ_306390,RMVar_hsa_circ_19454 39981 RMVar_ID_39981 Human_SNP_ID_115695193 A-to-I Human chr2 - 227706605 227706605 227706605 CACCGCAACCGACTAATTTTTGCGTTATTAGTAGAGATGGGGTTTCACTCTGTTGGCCAGGCTAG CACCGCAACCGACTAATTTTTGCGTTATTAGTGGAGATGGGGTTTCACTCTGTTGGCCAGGCTAG T C SLC19A3 Ensembl:ENSG00000135917 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1033449970 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_367363 39982 RMVar_ID_39982 Human_SNP_ID_115695194 A-to-I Human chr2 - 227706608 227706608 227706608 CACCACCGCAACCGACTAATTTTTGCGTTATTAGTAGAGATGGGGTTTCACTCTGTTGGCCAGGC CACCACCGCAACCGACTAATTTTTGCGTTATTGGTAGAGATGGGGTTTCACTCTGTTGGCCAGGC T C SLC19A3 Ensembl:ENSG00000135917 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs986179807 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_367363 39983 RMVar_ID_39983 Human_SNP_ID_116230785 A-to-I Human chr2 - 229834652 229834652 229834652 GGGTTCAAGTGATTCTCTTGCCTCAGCCTCCTAAGTAGTTGGGACTACAAGTGCCTGACACCACA GGGTTCAAGTGATTCTCTTGCCTCAGCCTCCTGAGTAGTTGGGACTACAAGTGCCTGACACCACA T C TRIP12 Ensembl:ENSG00000153827 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1261438448 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108938,RMVar_hsa_circ_207400,RMVar_hsa_circ_51495,RMVar_hsa_circ_127495,RMVar_hsa_circ_70364,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_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_124074,RMVar_hsa_circ_62327,RMVar_hsa_circ_72910,RMVar_hsa_circ_64837,RMVar_hsa_circ_207442,RMVar_hsa_circ_341547,RMVar_hsa_circ_207445,RMVar_hsa_circ_93959,RMVar_hsa_circ_353009,RMVar_hsa_circ_316470,RMVar_hsa_circ_340023,RMVar_hsa_circ_302932,RMVar_hsa_circ_294644,RMVar_hsa_circ_207446,RMVar_hsa_circ_207448,RMVar_hsa_circ_207447,RMVar_hsa_circ_343281,RMVar_hsa_circ_285171,RMVar_hsa_circ_285577,RMVar_hsa_circ_272497,RMVar_hsa_circ_207452,RMVar_hsa_circ_207453,RMVar_hsa_circ_207454 39984 RMVar_ID_39984 Human_SNP_ID_116251618 A-to-I Human chr2 - 229915870 229915870 229915870 AGCAACTTAGTAGAGACCTTGTTGCTACTAAAAGTAAAAAATTAGCTGGGCATGGTGGCACATGC AGCAACTTAGTAGAGACCTTGTTGCTACTAAATGTAAAAAATTAGCTGGGCATGGTGGCACATGC T A TRIP12 Ensembl:ENSG00000153827 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569183570 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13790960,Human_RBP_ID_17570213 RMVar_hsa_circ_207445,RMVar_hsa_circ_93959 39985 RMVar_ID_39985 Human_SNP_ID_116254854 A-to-I Human chr2 + 229926310 229926310 229926310 AAAATTAGCTGGGCATGGTGATGCACGCCTGTAGTCCTAGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTAGCTGGGCATGGTGATGCACGCCTGTGGTCCTAGCTACTCGGGAGGCTGAGGCAGGAGA A G FBXO36 Ensembl:ENSG00000153832 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1408746298 Functional Loss SNV dbSNP153 33..33 33 - - - 39986 RMVar_ID_39986 Human_SNP_ID_116257290 A-to-I Human chr2 + 229936041 229936041 229936041 AAAACCCCGTCTCTACTAAAAATACAAAAATTAGCTGGGTGTGGTGGTGGACGCTTGTAATCCCA AAAACCCCGTCTCTACTAAAAATACAAAAATTGGCTGGGTGTGGTGGTGGACGCTTGTAATCCCA A G FBXO36 Ensembl:ENSG00000153832 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1001815030 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72259 39987 RMVar_ID_39987 Human_SNP_ID_116314488 A-to-I Human chr2 + 230165695 230165695 230165695 ATAAACGCATTGCCTTAAGTATGTGACACATTACAGATATTTTATTTTTGACTTTGACATTAAAA ATAAACGCATTGCCTTAAGTATGTGACACATTGCAGATATTTTATTTTTGACTTTGACATTAAAA A G AC009950.1 Ensembl:ENSG00000225963 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1060759 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_4690,GWAS_ID_4691,GWAS_ID_4692,GWAS_ID_4693,GWAS_ID_4694,GWAS_ID_4695,GWAS_ID_4696,GWAS_ID_4697,GWAS_ID_4698,GWAS_ID_4699,GWAS_ID_4700,GWAS_ID_4701,GWAS_ID_4702,GWAS_ID_4703,GWAS_ID_4704 39988 RMVar_ID_39988 Human_SNP_ID_116314734 A-to-I Human chr2 + 230166660 230166660 230166660 CTTAGTTTGTTTTTCATAGTGATCTGAGTGTTAAAATTCTGTTAACTTTTATTGTTGTACCTGGG CTTAGTTTGTTTTTCATAGTGATCTGAGTGTTGAAATTCTGTTAACTTTTATTGTTGTACCTGGG A G AC009950.1 Ensembl:ENSG00000225963 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs13026121 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_4705,GWAS_ID_4706,GWAS_ID_4707,GWAS_ID_4708,GWAS_ID_4709,GWAS_ID_4710,GWAS_ID_4711,GWAS_ID_4712,GWAS_ID_4713,GWAS_ID_4714,GWAS_ID_4715,GWAS_ID_4716,GWAS_ID_4717,GWAS_ID_4718,GWAS_ID_4719,GWAS_ID_4720,GWAS_ID_4721,GWAS_ID_4722,GWAS_ID_4723 39989 RMVar_ID_39989 Human_SNP_ID_116314835 A-to-I Human chr2 - 230167170 230167170 230167170 TGAGCCTGGGAGGCAGAGGTCGCAGTGAGCCAAGAATGCACCACTGCACTCCAGCCTGGACAACA TGAGCCTGGGAGGCAGAGGTCGCAGTGAGCCAGGAATGCACCACTGCACTCCAGCCTGGACAACA T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs537401981 Functional Loss SNV dbSNP153 33..33 33 - - - 39990 RMVar_ID_39990 Human_SNP_ID_116400038 A-to-I Human chr2 + 230524869 230524869 230524869 ATTTAACATTACTAAGGACAAGAATTCTAGTTAATATGTAATTCTGTATATAAAATGTGCCAAGA ATTTAACATTACTAAGGACAAGAATTCTAGTTCATATGTAATTCTGTATATAAAATGTGCCAAGA A C SP100 Ensembl:ENSG00000067066 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048919426 Functional Loss SNV dbSNP153 33..33 33 - - - 39991 RMVar_ID_39991 Human_SNP_ID_116400039 A-to-I Human chr2 + 230524869 230524869 230524869 ATTTAACATTACTAAGGACAAGAATTCTAGTTAATATGTAATTCTGTATATAAAATGTGCCAAGA ATTTAACATTACTAAGGACAAGAATTCTAGTTGATATGTAATTCTGTATATAAAATGTGCCAAGA A G SP100 Ensembl:ENSG00000067066 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048919426 Functional Loss SNV dbSNP153 33..33 33 - - - 39992 RMVar_ID_39992 Human_SNP_ID_116444414 A-to-I Human chr2 - 230695079 230695079 230695079 CTCTGTCATCCAGGCTGGAGTGCAGTGGCGCAATCTCAGCTCACTGCAACCTCTGCCTCCTGGGT CTCTGTCATCCAGGCTGGAGTGCAGTGGCGCAGTCTCAGCTCACTGCAACCTCTGCCTCCTGGGT T C LINC01907 Ensembl:ENSG00000226125 lincRNA exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1326241367 Functional Loss SNV dbSNP153 33..33 33 - - - 39993 RMVar_ID_39993 Human_SNP_ID_116444415 A-to-I Human chr2 - 230695080 230695080 230695080 GCTCTGTCATCCAGGCTGGAGTGCAGTGGCGCAATCTCAGCTCACTGCAACCTCTGCCTCCTGGG GCTCTGTCATCCAGGCTGGAGTGCAGTGGCGCCATCTCAGCTCACTGCAACCTCTGCCTCCTGGG T G LINC01907 Ensembl:ENSG00000226125 lincRNA exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1408819456 Functional Loss SNV dbSNP153 33..33 33 - - - 39994 RMVar_ID_39994 Human_SNP_ID_116453602 A-to-I Human chr2 + 230730184 230730184 230730184 CAGGCTAGAGTTCAGCGGCACGATCATGGTTCACTTCAGCCTCGACCTCCTAGGCTCAAGTGATC CAGGCTAGAGTTCAGCGGCACGATCATGGTTCCCTTCAGCCTCGACCTCCTAGGCTCAAGTGATC A C CAB39 Ensembl:ENSG00000135932 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459629959 Functional Loss SNV dbSNP153 33..33 33 - - - 39995 RMVar_ID_39995 Human_SNP_ID_116535002 A-to-I Human chr2 + 231047419 231047419 231047419 TGAGAGTGCAGCTGGGAAGAACTCTGAACCAGAAGTCATCAGAGCTGAGGCATGGCCTTGAACAT TGAGAGTGCAGCTGGGAAGAACTCTGAACCAGGAGTCATCAGAGCTGAGGCATGGCCTTGAACAT A G C2orf72 Ensembl:ENSG00000204128 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1225719269 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571009,Human_RBP_ID_27287389,Human_RBP_ID_27478191,Human_RBP_ID_27563631 39996 RMVar_ID_39996 Human_SNP_ID_116543348 A-to-I Human chr2 + 231082606 231082606 231082606 AGCCACCTGTAATCCCAGCTACTTGAGAGGCTAAGGCAGGAGAATCACTTGAACCCAGGAGGTGG AGCCACCTGTAATCCCAGCTACTTGAGAGGCTGAGGCAGGAGAATCACTTGAACCCAGGAGGTGG A G PSMD1 Ensembl:ENSG00000173692 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1559223163 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84982,RMVar_hsa_circ_113288,RMVar_hsa_circ_207521,RMVar_hsa_circ_370018,RMVar_hsa_circ_2357,RMVar_hsa_circ_19072,RMVar_hsa_circ_7718,RMVar_hsa_circ_309949,RMVar_hsa_circ_79302,RMVar_hsa_circ_207522,RMVar_hsa_circ_207523,RMVar_hsa_circ_207524,RMVar_hsa_circ_274014,RMVar_hsa_circ_12296,RMVar_hsa_circ_101974,RMVar_hsa_circ_207525,RMVar_hsa_circ_69676,RMVar_hsa_circ_49026,RMVar_hsa_circ_207529,RMVar_hsa_circ_112925,RMVar_hsa_circ_355826,RMVar_hsa_circ_371629,RMVar_hsa_circ_207528,RMVar_hsa_circ_369372,RMVar_hsa_circ_347543,RMVar_hsa_circ_352037,RMVar_hsa_circ_270839,RMVar_hsa_circ_207531,RMVar_hsa_circ_207532,RMVar_hsa_circ_207533,RMVar_hsa_circ_207530,RMVar_hsa_circ_30361,RMVar_hsa_circ_80537,RMVar_hsa_circ_207535,RMVar_hsa_circ_91394,RMVar_hsa_circ_371157,RMVar_hsa_circ_4358,RMVar_hsa_circ_207536,RMVar_hsa_circ_16305,RMVar_hsa_circ_207537,RMVar_hsa_circ_64683,RMVar_hsa_circ_374402,RMVar_hsa_circ_207538 39997 RMVar_ID_39997 Human_SNP_ID_116544227 A-to-I Human chr2 + 231086313 231086313 231086313 CAATCCTCCTGTTTTGGCCTCTCAAAAGTGCTAGGATTACAGGTGTGAGCCACTGTGTCTGGCCA CAATCCTCCTGTTTTGGCCTCTCAAAAGTGCTCGGATTACAGGTGTGAGCCACTGTGTCTGGCCA A C PSMD1 Ensembl:ENSG00000173692 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444762705 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84982,RMVar_hsa_circ_113288,RMVar_hsa_circ_207521,RMVar_hsa_circ_370018,RMVar_hsa_circ_19072,RMVar_hsa_circ_309949,RMVar_hsa_circ_79302,RMVar_hsa_circ_207522,RMVar_hsa_circ_207523,RMVar_hsa_circ_207524,RMVar_hsa_circ_12296,RMVar_hsa_circ_101974,RMVar_hsa_circ_207525,RMVar_hsa_circ_69676,RMVar_hsa_circ_49026,RMVar_hsa_circ_207529,RMVar_hsa_circ_112925,RMVar_hsa_circ_355826,RMVar_hsa_circ_371629,RMVar_hsa_circ_207528,RMVar_hsa_circ_369372,RMVar_hsa_circ_347543,RMVar_hsa_circ_270839,RMVar_hsa_circ_207531,RMVar_hsa_circ_207532,RMVar_hsa_circ_207533,RMVar_hsa_circ_207530,RMVar_hsa_circ_80537,RMVar_hsa_circ_207535,RMVar_hsa_circ_91394,RMVar_hsa_circ_371157,RMVar_hsa_circ_4358,RMVar_hsa_circ_207536,RMVar_hsa_circ_207537,RMVar_hsa_circ_64683,RMVar_hsa_circ_374402,RMVar_hsa_circ_207538 39998 RMVar_ID_39998 Human_SNP_ID_116544228 A-to-I Human chr2 + 231086313 231086313 231086313 CAATCCTCCTGTTTTGGCCTCTCAAAAGTGCTAGGATTACAGGTGTGAGCCACTGTGTCTGGCCA CAATCCTCCTGTTTTGGCCTCTCAAAAGTGCTGGGATTACAGGTGTGAGCCACTGTGTCTGGCCA A G PSMD1 Ensembl:ENSG00000173692 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444762705 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84982,RMVar_hsa_circ_113288,RMVar_hsa_circ_207521,RMVar_hsa_circ_370018,RMVar_hsa_circ_19072,RMVar_hsa_circ_309949,RMVar_hsa_circ_79302,RMVar_hsa_circ_207522,RMVar_hsa_circ_207523,RMVar_hsa_circ_207524,RMVar_hsa_circ_12296,RMVar_hsa_circ_101974,RMVar_hsa_circ_207525,RMVar_hsa_circ_69676,RMVar_hsa_circ_49026,RMVar_hsa_circ_207529,RMVar_hsa_circ_112925,RMVar_hsa_circ_355826,RMVar_hsa_circ_371629,RMVar_hsa_circ_207528,RMVar_hsa_circ_369372,RMVar_hsa_circ_347543,RMVar_hsa_circ_270839,RMVar_hsa_circ_207531,RMVar_hsa_circ_207532,RMVar_hsa_circ_207533,RMVar_hsa_circ_207530,RMVar_hsa_circ_80537,RMVar_hsa_circ_207535,RMVar_hsa_circ_91394,RMVar_hsa_circ_371157,RMVar_hsa_circ_4358,RMVar_hsa_circ_207536,RMVar_hsa_circ_207537,RMVar_hsa_circ_64683,RMVar_hsa_circ_374402,RMVar_hsa_circ_207538 39999 RMVar_ID_39999 Human_SNP_ID_116562600 A-to-I Human chr2 + 231165879 231165879 231165879 CTTTTTTTAAATTTTATTTTATAGGATGAGGCAGAGAAAAAGGAGGAAAAAGAGAAGAAAAAAGA CTTTTTTTAAATTTTATTTTATAGGATGAGGCTGAGAAAAAGGAGGAAAAAGAGAAGAAAAAAGA A T PSMD1 Ensembl:ENSG00000173692 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1386203761 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9096,Human_RBP_ID_60327,Human_RBP_ID_2626856,Human_RBP_ID_22998796,Human_RBP_ID_24546565,Human_RBP_ID_25586835,Human_RBP_ID_26340332,Human_RBP_ID_27818037 Human_Splice_Rec_369436,Human_Splice_Rec_369524,Human_Splice_Rec_369580,Human_Splice_Rec_369624,Human_Splice_Rec_369652 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 40000 RMVar_ID_40000 Human_SNP_ID_116592548 A-to-I Human chr2 + 231287611 231287611 231287611 TCACTATGTCACCAGGCTGGTCTCGAACTCCTAGGCTCAAGCGATTCTCCTGCCTCAGCCTCCCA TCACTATGTCACCAGGCTGGTCTCGAACTCCTCGGCTCAAGCGATTCTCCTGCCTCAGCCTCCCA A C ARMC9 Ensembl:ENSG00000135931 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1160578509 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_343695,RMVar_hsa_circ_343518,RMVar_hsa_circ_308200,RMVar_hsa_circ_63123,RMVar_hsa_circ_53072,RMVar_hsa_circ_11571,RMVar_hsa_circ_14482,RMVar_hsa_circ_11180,RMVar_hsa_circ_207547,RMVar_hsa_circ_50929,RMVar_hsa_circ_31011,RMVar_hsa_circ_300100,RMVar_hsa_circ_3396,RMVar_hsa_circ_283968,RMVar_hsa_circ_16952,RMVar_hsa_circ_120169,RMVar_hsa_circ_207568,RMVar_hsa_circ_207574,RMVar_hsa_circ_51104,RMVar_hsa_circ_337609,RMVar_hsa_circ_46727,RMVar_hsa_circ_282477,RMVar_hsa_circ_327994,RMVar_hsa_circ_207577,RMVar_hsa_circ_321159,RMVar_hsa_circ_22750,RMVar_hsa_circ_281241,RMVar_hsa_circ_207579,RMVar_hsa_circ_320267,RMVar_hsa_circ_46673 40001 RMVar_ID_40001 Human_SNP_ID_116596456 A-to-I Human chr2 + 231304426 231304426 231304426 CCAAATTTTTTGTTTGTTTGAGACGAAGTCTCACTCTATCGCCCAGGCTGGAGTGCAATGGTGCC CCAAATTTTTTGTTTGTTTGAGACGAAGTCTCTCTCTATCGCCCAGGCTGGAGTGCAATGGTGCC A T ARMC9 Ensembl:ENSG00000135931 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1211801682 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_343695,RMVar_hsa_circ_343518,RMVar_hsa_circ_53072,RMVar_hsa_circ_11571,RMVar_hsa_circ_14482,RMVar_hsa_circ_50929,RMVar_hsa_circ_16952,RMVar_hsa_circ_321159,RMVar_hsa_circ_22750,RMVar_hsa_circ_320267,RMVar_hsa_circ_46673,RMVar_hsa_circ_332859,RMVar_hsa_circ_29017 40002 RMVar_ID_40002 Human_SNP_ID_116601476 A-to-I Human chr2 + 231324651 231324651 231324651 CTATAATCCCAGCTACTCGGGAGGCTGAGGCGAGAGAATCACTTGAACCGAGGAGGCGGAGGTTG CTATAATCCCAGCTACTCGGGAGGCTGAGGCGGGAGAATCACTTGAACCGAGGAGGCGGAGGTTG A G ARMC9 Ensembl:ENSG00000135931 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs887778514 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_343695,RMVar_hsa_circ_343518,RMVar_hsa_circ_53072,RMVar_hsa_circ_11571,RMVar_hsa_circ_14482,RMVar_hsa_circ_50929,RMVar_hsa_circ_16952,RMVar_hsa_circ_321159,RMVar_hsa_circ_22750,RMVar_hsa_circ_320267,RMVar_hsa_circ_46673,RMVar_hsa_circ_332859,RMVar_hsa_circ_29017 40003 RMVar_ID_40003 Human_SNP_ID_116601479 A-to-I Human chr2 + 231324659 231324659 231324659 CCAGCTACTCGGGAGGCTGAGGCGAGAGAATCACTTGAACCGAGGAGGCGGAGGTTGTGGTGAGT CCAGCTACTCGGGAGGCTGAGGCGAGAGAATCGCTTGAACCGAGGAGGCGGAGGTTGTGGTGAGT A G ARMC9 Ensembl:ENSG00000135931 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1036989733 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_343695,RMVar_hsa_circ_343518,RMVar_hsa_circ_53072,RMVar_hsa_circ_11571,RMVar_hsa_circ_14482,RMVar_hsa_circ_50929,RMVar_hsa_circ_16952,RMVar_hsa_circ_321159,RMVar_hsa_circ_22750,RMVar_hsa_circ_320267,RMVar_hsa_circ_46673,RMVar_hsa_circ_332859,RMVar_hsa_circ_29017 40004 RMVar_ID_40004 Human_SNP_ID_116637005 A-to-I Human chr2 - 231459605 231459605 231459605 ACCCTGCCAGTAAGTTTTAATAATTTGGTGTTAGGTGGGAGAATCGCTTGAACCTGGGAGGCAGA ACCCTGCCAGTAAGTTTTAATAATTTGGTGTTGGGTGGGAGAATCGCTTGAACCTGGGAGGCAGA T C NCL Ensembl:ENSG00000115053 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs796539716 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8513800,Human_RBP_ID_13794746 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_62733,RMVar_hsa_circ_301036,RMVar_hsa_circ_365323 40005 RMVar_ID_40005 Human_SNP_ID_116637084 A-to-I Human chr2 - 231459861 231459861 231459861 TGGCTTTTGCTCAGGCTGGAGTACAGTGGCGCAATCTTGGCTCACTGCAACCTCTGCCTCCCGGG TGGCTTTTGCTCAGGCTGGAGTACAGTGGCGCGATCTTGGCTCACTGCAACCTCTGCCTCCCGGG T C NCL Ensembl:ENSG00000115053 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs926969500 Functional Loss SNV dbSNP153 33..33 33 - - - 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_62733,RMVar_hsa_circ_301036,RMVar_hsa_circ_365323 40006 RMVar_ID_40006 Human_SNP_ID_116637092 A-to-I Human chr2 - 231459871 231459871 231459871 AGACGGACGCTGGCTTTTGCTCAGGCTGGAGTACAGTGGCGCAATCTTGGCTCACTGCAACCTCT AGACGGACGCTGGCTTTTGCTCAGGCTGGAGTGCAGTGGCGCAATCTTGGCTCACTGCAACCTCT T C NCL Ensembl:ENSG00000115053 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1221120486 Functional Loss SNV dbSNP153 33..33 33 - - - 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_62733,RMVar_hsa_circ_301036,RMVar_hsa_circ_365323 40007 RMVar_ID_40007 Human_SNP_ID_116643173 A-to-I Human chr2 - 231481297 231481297 231481297 CAAAAATTAGCCAGGTGTGGTGGCAGGCACCTATAACCCCAGCTACTTGGGAGTCTGAGGCAGAA CAAAAATTAGCCAGGTGTGGTGGCAGGCACCTGTAACCCCAGCTACTTGGGAGTCTGAGGCAGAA T C NCL Ensembl:ENSG00000115053 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1201810932 Functional Loss SNV dbSNP153 33..33 33 - - - 40008 RMVar_ID_40008 Human_SNP_ID_116646754 A-to-I Human chr2 - 231496088 231496088 231496088 TGGTGTTGCATACCTGTAGTCCTAGCTAACTCAGGAGACTGAGGTAGGAGGATTGCCTGAGCCTG TGGTGTTGCATACCTGTAGTCCTAGCTAACTCGGGAGACTGAGGTAGGAGGATTGCCTGAGCCTG T C LINC00471,LINC00471:2,LINC00471:3 RNACentral:URS0000D5D405,RNACentral:URS0000D59D94,RNACentral:URS0000D5A869 lincRNA,lincRNA,lincRNA exon,exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs923413129 Functional Loss SNV dbSNP153 33..33 33 - - - 40009 RMVar_ID_40009 Human_SNP_ID_116646756 A-to-I Human chr2 - 231496097 231496097 231496097 AGCTGGGCGTGGTGTTGCATACCTGTAGTCCTAGCTAACTCAGGAGACTGAGGTAGGAGGATTGC AGCTGGGCGTGGTGTTGCATACCTGTAGTCCTGGCTAACTCAGGAGACTGAGGTAGGAGGATTGC T C LINC00471,LINC00471:2,LINC00471:3 RNACentral:URS0000D5D405,RNACentral:URS0000D59D94,RNACentral:URS0000D5A869 lincRNA,lincRNA,lincRNA exon,exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs573529130 Functional Loss SNV dbSNP153 33..33 33 - - - 40010 RMVar_ID_40010 Human_SNP_ID_116647311 A-to-I Human chr2 - 231498473 231498473 231498473 AAATTAGCCAGGCGCGGCGGTGAGCGCCTGTAATCCCAGCTACTTGGGAGACTGAGGCAGGAGAA AAATTAGCCAGGCGCGGCGGTGAGCGCCTGTAGTCCCAGCTACTTGGGAGACTGAGGCAGGAGAA T C AC017104.5 Ensembl:ENSG00000283491 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350800815 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17393962 RMVar_hsa_circ_207595 40011 RMVar_ID_40011 Human_SNP_ID_116648580 A-to-I Human chr2 - 231503501 231503501 231503501 CAGTGGTGCGATCTTGGCTCACTGCAACCTCCACCTCCCGTGTTCAAGCCATTCTCCTGCCTCAG CAGTGGTGCGATCTTGGCTCACTGCAACCTCCGCCTCCCGTGTTCAAGCCATTCTCCTGCCTCAG T C AC017104.5 Ensembl:ENSG00000283491 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1020007662 Functional Loss SNV dbSNP153 33..33 33 - - - 40012 RMVar_ID_40012 Human_SNP_ID_116648581 A-to-I Human chr2 - 231503501 231503501 231503501 CAGTGGTGCGATCTTGGCTCACTGCAACCTCCACCTCCCGTGTTCAAGCCATTCTCCTGCCTCAG CAGTGGTGCGATCTTGGCTCACTGCAACCTCCCCCTCCCGTGTTCAAGCCATTCTCCTGCCTCAG T G AC017104.5 Ensembl:ENSG00000283491 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1020007662 Functional Loss SNV dbSNP153 33..33 33 - - - 40013 RMVar_ID_40013 Human_SNP_ID_116648585 A-to-I Human chr2 - 231503513 231503513 231503513 CAGGCTGGAGTGCAGTGGTGCGATCTTGGCTCACTGCAACCTCCACCTCCCGTGTTCAAGCCATT CAGGCTGGAGTGCAGTGGTGCGATCTTGGCTCGCTGCAACCTCCACCTCCCGTGTTCAAGCCATT T C AC017104.5 Ensembl:ENSG00000283491 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1267264880 Functional Loss SNV dbSNP153 33..33 33 - - - 40014 RMVar_ID_40014 Human_SNP_ID_116649116 A-to-I Human chr2 - 231505736 231505736 231505736 TTGCGCAGACTGGTCCTGAACTCCTGGTCTCAAGTGATCCGTCAGTCTCAGCCTCCCAGAGTGCT TTGCGCAGACTGGTCCTGAACTCCTGGTCTCAGGTGATCCGTCAGTCTCAGCCTCCCAGAGTGCT T C AC017104.5 Ensembl:ENSG00000283491 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1157800270 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17393972 40015 RMVar_ID_40015 Human_SNP_ID_116649154 A-to-I Human chr2 - 231505867 231505867 231505867 TTACTGTAGTCTCTACCTTCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTAAGA TTACTGTAGTCTCTACCTTCCAGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCCGAGTAGCTAAGA T C AC017104.5 Ensembl:ENSG00000283491 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1339883489 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17393973 40016 RMVar_ID_40016 Human_SNP_ID_116703335 A-to-I Human chr2 - 231705810 231705810 231705810 AAAATTAGCCGGGCCTGGTGGCGTGCGCCTGTAATCCCAGCTACTCGGGAGGCTGAGACAGGAGA AAAATTAGCCGGGCCTGGTGGCGTGCGCCTGTTATCCCAGCTACTCGGGAGGCTGAGACAGGAGA T A lnc-PDE6D-3,lnc-PDE6D-3:2 RNACentral:URS00008B5F3E,RNACentral:URS00008B6EFF lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886397987 Functional Loss SNV dbSNP153 33..33 33 - - - 40017 RMVar_ID_40017 Human_SNP_ID_116717797 A-to-I Human chr2 - 231757019 231757019 231757019 AGGAAGTTGAGGCTGCAGTGAGCTGTGATCGTACCACTGCACTCCAGCCTGGGCAACAGGAGTGA AGGAAGTTGAGGCTGCAGTGAGCTGTGATCGTGCCACTGCACTCCAGCCTGGGCAACAGGAGTGA T C PDE6D Ensembl:ENSG00000156973 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1476911137 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25520510 40018 RMVar_ID_40018 Human_SNP_ID_116719290 A-to-I Human chr2 - 231763840 231763840 231763840 GAGCCCAGGAATTCAAGACCGGCCTGAGCAACATAGACTCTGTCTCAACAGCAACAACAAAAATT GAGCCCAGGAATTCAAGACCGGCCTGAGCAACTTAGACTCTGTCTCAACAGCAACAACAAAAATT T A PDE6D Ensembl:ENSG00000156973 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs920774080 Functional Loss SNV dbSNP153 33..33 33 - - - 40019 RMVar_ID_40019 Human_SNP_ID_116719291 A-to-I Human chr2 - 231763840 231763840 231763840 GAGCCCAGGAATTCAAGACCGGCCTGAGCAACATAGACTCTGTCTCAACAGCAACAACAAAAATT GAGCCCAGGAATTCAAGACCGGCCTGAGCAACGTAGACTCTGTCTCAACAGCAACAACAAAAATT T C PDE6D Ensembl:ENSG00000156973 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs920774080 Functional Loss SNV dbSNP153 33..33 33 - - - 40020 RMVar_ID_40020 Human_SNP_ID_116719877 A-to-I Human chr2 - 231766767 231766767 231766767 GGTCTCAAACTCCCCCTGACCTCAGATGATCCACCCTTCTCAGCCTTCCAAAGTACTGGGATAAT GGTCTCAAACTCCCCCTGACCTCAGATGATCCGCCCTTCTCAGCCTTCCAAAGTACTGGGATAAT T C PDE6D Ensembl:ENSG00000156973 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs997468066 Functional Loss SNV dbSNP153 33..33 33 - - - 40021 RMVar_ID_40021 Human_SNP_ID_116721328 A-to-I Human chr2 - 231773165 231773165 231773165 GCTATCATAGCTTACTGCAGCCTTGACCTCCCAGGCTCAGATGATCCTCTGCCTCACCCTCCTGA GCTATCATAGCTTACTGCAGCCTTGACCTCCCGGGCTCAGATGATCCTCTGCCTCACCCTCCTGA T C PDE6D Ensembl:ENSG00000156973 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs981507708 Functional Loss SNV dbSNP153 33..33 33 - - - 40022 RMVar_ID_40022 Human_SNP_ID_116873138 A-to-I Human chr2 + 232311448 232311448 232311448 AACACATCCATGTCAAGAAATAGAACATGGCCAGGTGCAGTGGCTCACACCTATAATCCCAGCAC AACACATCCATGTCAAGAAATAGAACATGGCCGGGTGCAGTGGCTCACACCTATAATCCCAGCAC A G DIS3L2 Ensembl:ENSG00000144535 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs937210104 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94687,RMVar_hsa_circ_207622,RMVar_hsa_circ_112846,RMVar_hsa_circ_86210,RMVar_hsa_circ_207630,RMVar_hsa_circ_103120,RMVar_hsa_circ_95796,RMVar_hsa_circ_207635,RMVar_hsa_circ_207636,RMVar_hsa_circ_207637 40023 RMVar_ID_40023 Human_SNP_ID_116883681 A-to-I Human chr2 + 232348133 232348133 232348133 TCGGCTTACTGCAGCCTCCACCTCCCGGGTTCAAGTGATTATCCTGCCTCAGCCTCCAGAATAGC TCGGCTTACTGCAGCCTCCACCTCCCGGGTTCTAGTGATTATCCTGCCTCAGCCTCCAGAATAGC A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1330395036 Functional Loss SNV dbSNP153 33..33 33 - - - 40024 RMVar_ID_40024 Human_SNP_ID_116890663 A-to-I Human chr2 - 232374834 232374834 232374834 CCAAGAGATTCTTCCACCTCAGCCTCCCGAGTAGTGGGGACTACAGGTGTGTGCCACCTTGCCCA CCAAGAGATTCTTCCACCTCAGCCTCCCGAGTGGTGGGGACTACAGGTGTGTGCCACCTTGCCCA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1294391122 Functional Loss SNV dbSNP153 33..33 33 - - - 40025 RMVar_ID_40025 Human_SNP_ID_116940494 A-to-I Human chr2 - 232547306 232547306 232547306 TCAAGCGATCCTCCCACCTCAGCCTCCCGAGTAACTGGGACTACAGGCATGCATCACCACGCCCA TCAAGCGATCCTCCCACCTCAGCCTCCCGAGTGACTGGGACTACAGGCATGCATCACCACGCCCA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1318065270 Functional Loss SNV dbSNP153 33..33 33 - - - 40026 RMVar_ID_40026 Human_SNP_ID_116967938 A-to-I Human chr2 + 232651701 232651701 232651701 AAAATTAGCTAGGCGTGGTGGCAGGGTCCTGTAGTCCCACCTACTCAGGAGGCTGAGGCAAGAGA AAAATTAGCTAGGCGTGGTGGCAGGGTCCTGTGGTCCCACCTACTCAGGAGGCTGAGGCAAGAGA A G EFHD1 Ensembl:ENSG00000115468 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs963579311 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82958,RMVar_hsa_circ_207652 40027 RMVar_ID_40027 Human_SNP_ID_116970638 A-to-I Human chr2 + 232661749 232661748 232661750 GCCCAGCTAATTTTTGTATTTTTAGTAGAAACAGGGTTTCACCATGTTTGCCAGGCTGGTCTACG GCCCAGCTAATTTTTGTATTTTTAGTAGAAAC__GGTTTCACCATGTTTGCCAGGCTGGTCTACG CAG C EFHD1 Ensembl:ENSG00000115468 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs111401199 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_82958,RMVar_hsa_circ_207652 40028 RMVar_ID_40028 Human_SNP_ID_116970642 A-to-I Human chr2 + 232661749 232661749 232661749 GCCCAGCTAATTTTTGTATTTTTAGTAGAAACAGGGTTTCACCATGTTTGCCAGGCTGGTCTACG GCCCAGCTAATTTTTGTATTTTTAGTAGAAACGGGGTTTCACCATGTTTGCCAGGCTGGTCTACG A G EFHD1 Ensembl:ENSG00000115468 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs113909507 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82958,RMVar_hsa_circ_207652 40029 RMVar_ID_40029 Human_SNP_ID_116981012 A-to-I Human chr2 + 232701607 232701607 232701607 CCATGCCACCACATCTGGCCAATATTTTTTGTAGAGATGGGGTCTCACTATGTTGCCTAGGCTGG CCATGCCACCACATCTGGCCAATATTTTTTGTGGAGATGGGGTCTCACTATGTTGCCTAGGCTGG A G GIGYF2 Ensembl:ENSG00000204120 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1049553681 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3560,RMVar_hsa_circ_55303,RMVar_hsa_circ_85327,RMVar_hsa_circ_112145,RMVar_hsa_circ_207653,RMVar_hsa_circ_207654,RMVar_hsa_circ_71108,RMVar_hsa_circ_108369,RMVar_hsa_circ_358619,RMVar_hsa_circ_104270,RMVar_hsa_circ_46578,RMVar_hsa_circ_207655,RMVar_hsa_circ_207656 40030 RMVar_ID_40030 Human_SNP_ID_116981026 A-to-I Human chr2 + 232701684 232701684 232701684 GGTCTCAAGTGATACTCCCGCTTCAGCTTCCCAAAGTGTTGAGATTATAGGCATGAGCCACTGTG GGTCTCAAGTGATACTCCCGCTTCAGCTTCCCCAAGTGTTGAGATTATAGGCATGAGCCACTGTG A C GIGYF2 Ensembl:ENSG00000204120 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1368110009 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13797274 RMVar_hsa_circ_3560,RMVar_hsa_circ_55303,RMVar_hsa_circ_85327,RMVar_hsa_circ_112145,RMVar_hsa_circ_207653,RMVar_hsa_circ_207654,RMVar_hsa_circ_71108,RMVar_hsa_circ_108369,RMVar_hsa_circ_358619,RMVar_hsa_circ_104270,RMVar_hsa_circ_46578,RMVar_hsa_circ_207655,RMVar_hsa_circ_207656 40031 RMVar_ID_40031 Human_SNP_ID_116981027 A-to-I Human chr2 + 232701684 232701684 232701684 GGTCTCAAGTGATACTCCCGCTTCAGCTTCCCAAAGTGTTGAGATTATAGGCATGAGCCACTGTG GGTCTCAAGTGATACTCCCGCTTCAGCTTCCCTAAGTGTTGAGATTATAGGCATGAGCCACTGTG A T GIGYF2 Ensembl:ENSG00000204120 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1368110009 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13797274 RMVar_hsa_circ_3560,RMVar_hsa_circ_55303,RMVar_hsa_circ_85327,RMVar_hsa_circ_112145,RMVar_hsa_circ_207653,RMVar_hsa_circ_207654,RMVar_hsa_circ_71108,RMVar_hsa_circ_108369,RMVar_hsa_circ_358619,RMVar_hsa_circ_104270,RMVar_hsa_circ_46578,RMVar_hsa_circ_207655,RMVar_hsa_circ_207656 40032 RMVar_ID_40032 Human_SNP_ID_116981035 A-to-I Human chr2 + 232701704 232701704 232701704 CTTCAGCTTCCCAAAGTGTTGAGATTATAGGCATGAGCCACTGTGCCCCACCAAGAATGCAATTT CTTCAGCTTCCCAAAGTGTTGAGATTATAGGCGTGAGCCACTGTGCCCCACCAAGAATGCAATTT A G GIGYF2 Ensembl:ENSG00000204120 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs557803922 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13797274 RMVar_hsa_circ_3560,RMVar_hsa_circ_55303,RMVar_hsa_circ_85327,RMVar_hsa_circ_112145,RMVar_hsa_circ_207653,RMVar_hsa_circ_207654,RMVar_hsa_circ_71108,RMVar_hsa_circ_108369,RMVar_hsa_circ_358619,RMVar_hsa_circ_104270,RMVar_hsa_circ_46578,RMVar_hsa_circ_207655,RMVar_hsa_circ_207656 40033 RMVar_ID_40033 Human_SNP_ID_116981297 A-to-I Human chr2 + 232702826 232702826 232702826 TGTTAGATATATATTTTTTGAGATAAGGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGTACA TGTTAGATATATATTTTTTGAGATAAGGTCTCGCTCTGTCACCCAGGCTGGAGTGCAGTGGTACA A G GIGYF2 Ensembl:ENSG00000204120 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs180888061 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3560,RMVar_hsa_circ_55303,RMVar_hsa_circ_85327,RMVar_hsa_circ_112145,RMVar_hsa_circ_207653,RMVar_hsa_circ_207654,RMVar_hsa_circ_71108,RMVar_hsa_circ_108369,RMVar_hsa_circ_358619,RMVar_hsa_circ_104270,RMVar_hsa_circ_46578,RMVar_hsa_circ_207655,RMVar_hsa_circ_207656 40034 RMVar_ID_40034 Human_SNP_ID_116981322 A-to-I Human chr2 + 232702941 232702941 232702941 CCTCAGCTTCCCGAGTAGCTGGGACTACAGGCATGTGCCACCATGCCTGGCTAATTTTTGTAGAG CCTCAGCTTCCCGAGTAGCTGGGACTACAGGCGTGTGCCACCATGCCTGGCTAATTTTTGTAGAG A G GIGYF2 Ensembl:ENSG00000204120 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1391681037 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3560,RMVar_hsa_circ_55303,RMVar_hsa_circ_85327,RMVar_hsa_circ_112145,RMVar_hsa_circ_207653,RMVar_hsa_circ_207654,RMVar_hsa_circ_71108,RMVar_hsa_circ_108369,RMVar_hsa_circ_358619,RMVar_hsa_circ_104270,RMVar_hsa_circ_46578,RMVar_hsa_circ_207655,RMVar_hsa_circ_207656 40035 RMVar_ID_40035 Human_SNP_ID_116982030 A-to-I Human chr2 + 232705483 232705483 232705483 GAGGCTGGAGCACAATGGCGTGATCTCGGCTCACCACATCCTCTGCCTCCTGGGCTCAAGCAGTT GAGGCTGGAGCACAATGGCGTGATCTCGGCTCGCCACATCCTCTGCCTCCTGGGCTCAAGCAGTT A G GIGYF2 Ensembl:ENSG00000204120 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1405043517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_371708 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_108369,RMVar_hsa_circ_358619,RMVar_hsa_circ_104270,RMVar_hsa_circ_46578,RMVar_hsa_circ_38430,RMVar_hsa_circ_308150,RMVar_hsa_circ_207655,RMVar_hsa_circ_207656,RMVar_hsa_circ_350608,RMVar_hsa_circ_377989,RMVar_hsa_circ_312500,RMVar_hsa_circ_63959,RMVar_hsa_circ_306686,RMVar_hsa_circ_49770,RMVar_hsa_circ_207657,RMVar_hsa_circ_207658 40036 RMVar_ID_40036 Human_SNP_ID_116982032 A-to-I Human chr2 + 232705486 232705486 232705486 GCTGGAGCACAATGGCGTGATCTCGGCTCACCACATCCTCTGCCTCCTGGGCTCAAGCAGTTCTG GCTGGAGCACAATGGCGTGATCTCGGCTCACCGCATCCTCTGCCTCCTGGGCTCAAGCAGTTCTG A G GIGYF2 Ensembl:ENSG00000204120 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs10427392 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25586933 Human_Splice_Rec_371708 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_108369,RMVar_hsa_circ_358619,RMVar_hsa_circ_104270,RMVar_hsa_circ_46578,RMVar_hsa_circ_38430,RMVar_hsa_circ_308150,RMVar_hsa_circ_207655,RMVar_hsa_circ_207656,RMVar_hsa_circ_350608,RMVar_hsa_circ_377989,RMVar_hsa_circ_312500,RMVar_hsa_circ_63959,RMVar_hsa_circ_306686,RMVar_hsa_circ_49770,RMVar_hsa_circ_207657,RMVar_hsa_circ_207658 40037 RMVar_ID_40037 Human_SNP_ID_116982033 A-to-I Human chr2 + 232705486 232705486 232705486 GCTGGAGCACAATGGCGTGATCTCGGCTCACCACATCCTCTGCCTCCTGGGCTCAAGCAGTTCTG GCTGGAGCACAATGGCGTGATCTCGGCTCACCTCATCCTCTGCCTCCTGGGCTCAAGCAGTTCTG A T GIGYF2 Ensembl:ENSG00000204120 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs10427392 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25586933 Human_Splice_Rec_371708 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_108369,RMVar_hsa_circ_358619,RMVar_hsa_circ_104270,RMVar_hsa_circ_46578,RMVar_hsa_circ_38430,RMVar_hsa_circ_308150,RMVar_hsa_circ_207655,RMVar_hsa_circ_207656,RMVar_hsa_circ_350608,RMVar_hsa_circ_377989,RMVar_hsa_circ_312500,RMVar_hsa_circ_63959,RMVar_hsa_circ_306686,RMVar_hsa_circ_49770,RMVar_hsa_circ_207657,RMVar_hsa_circ_207658 40038 RMVar_ID_40038 Human_SNP_ID_116982066 A-to-I Human chr2 + 232705585 232705585 232705585 GCGCCACCACACCCCGCTAATTTTGTATTTGTAGTAGAGACAGGGTTTCTCCATGTTGGTCAGGC GCGCCACCACACCCCGCTAATTTTGTATTTGTGGTAGAGACAGGGTTTCTCCATGTTGGTCAGGC A G GIGYF2 Ensembl:ENSG00000204120 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs561796699 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_108369,RMVar_hsa_circ_358619,RMVar_hsa_circ_104270,RMVar_hsa_circ_46578,RMVar_hsa_circ_38430,RMVar_hsa_circ_308150,RMVar_hsa_circ_207655,RMVar_hsa_circ_207656,RMVar_hsa_circ_350608,RMVar_hsa_circ_377989,RMVar_hsa_circ_312500,RMVar_hsa_circ_63959,RMVar_hsa_circ_306686,RMVar_hsa_circ_49770,RMVar_hsa_circ_207657,RMVar_hsa_circ_207658 40039 RMVar_ID_40039 Human_SNP_ID_116982067 A-to-I Human chr2 + 232705588 232705588 232705588 CCACCACACCCCGCTAATTTTGTATTTGTAGTAGAGACAGGGTTTCTCCATGTTGGTCAGGCAGG CCACCACACCCCGCTAATTTTGTATTTGTAGTGGAGACAGGGTTTCTCCATGTTGGTCAGGCAGG A G GIGYF2 Ensembl:ENSG00000204120 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs891294021 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_108369,RMVar_hsa_circ_358619,RMVar_hsa_circ_104270,RMVar_hsa_circ_46578,RMVar_hsa_circ_38430,RMVar_hsa_circ_308150,RMVar_hsa_circ_207655,RMVar_hsa_circ_207656,RMVar_hsa_circ_350608,RMVar_hsa_circ_377989,RMVar_hsa_circ_312500,RMVar_hsa_circ_63959,RMVar_hsa_circ_306686,RMVar_hsa_circ_49770,RMVar_hsa_circ_207657,RMVar_hsa_circ_207658 40040 RMVar_ID_40040 Human_SNP_ID_116982092 A-to-I Human chr2 + 232705665 232705665 232705665 GACCTCAGGTTATCCGCCCGCCTTGGCCTCCCAAAGTACTGGGATTACAGGCGTGAGCCACCGTG GACCTCAGGTTATCCGCCCGCCTTGGCCTCCCGAAGTACTGGGATTACAGGCGTGAGCCACCGTG A G GIGYF2 Ensembl:ENSG00000204120 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1021904197 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_108369,RMVar_hsa_circ_358619,RMVar_hsa_circ_104270,RMVar_hsa_circ_46578,RMVar_hsa_circ_38430,RMVar_hsa_circ_308150,RMVar_hsa_circ_207655,RMVar_hsa_circ_207656,RMVar_hsa_circ_350608,RMVar_hsa_circ_377989,RMVar_hsa_circ_312500,RMVar_hsa_circ_63959,RMVar_hsa_circ_306686,RMVar_hsa_circ_49770,RMVar_hsa_circ_207657,RMVar_hsa_circ_207658 40041 RMVar_ID_40041 Human_SNP_ID_116982094 A-to-I Human chr2 + 232705679 232705679 232705679 CGCCCGCCTTGGCCTCCCAAAGTACTGGGATTACAGGCGTGAGCCACCGTGTGTGGCCTTTATTT CGCCCGCCTTGGCCTCCCAAAGTACTGGGATTGCAGGCGTGAGCCACCGTGTGTGGCCTTTATTT A G GIGYF2 Ensembl:ENSG00000204120 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1047566522 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_108369,RMVar_hsa_circ_358619,RMVar_hsa_circ_104270,RMVar_hsa_circ_46578,RMVar_hsa_circ_38430,RMVar_hsa_circ_308150,RMVar_hsa_circ_207655,RMVar_hsa_circ_207656,RMVar_hsa_circ_350608,RMVar_hsa_circ_377989,RMVar_hsa_circ_312500,RMVar_hsa_circ_63959,RMVar_hsa_circ_306686,RMVar_hsa_circ_49770,RMVar_hsa_circ_207657,RMVar_hsa_circ_207658 40042 RMVar_ID_40042 Human_SNP_ID_116987210 A-to-I Human chr2 + 232724689 232724689 232724689 CTCCCACCTCAGCCTCCCAAGTAGCTGGGACTAAGGCAAGTACCACCATACCTGGCTAATTAAAA CTCCCACCTCAGCCTCCCAAGTAGCTGGGACTGAGGCAAGTACCACCATACCTGGCTAATTAAAA A G GIGYF2 Ensembl:ENSG00000204120 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs548294671 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_108369,RMVar_hsa_circ_358619,RMVar_hsa_circ_104270,RMVar_hsa_circ_46578,RMVar_hsa_circ_83906,RMVar_hsa_circ_38430,RMVar_hsa_circ_308150,RMVar_hsa_circ_207655,RMVar_hsa_circ_207656,RMVar_hsa_circ_350608,RMVar_hsa_circ_377989,RMVar_hsa_circ_312500,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_276907,RMVar_hsa_circ_207660 40043 RMVar_ID_40043 Human_SNP_ID_116987769 A-to-I Human chr2 + 232727026 232727026 232727026 TTGCTCTGTTGCCCAGGCTGGAGTGCAGTGGCACGATGTCAGCTCACTGTAGCCTCTGCCTCCAG TTGCTCTGTTGCCCAGGCTGGAGTGCAGTGGCGCGATGTCAGCTCACTGTAGCCTCTGCCTCCAG A G GIGYF2 Ensembl:ENSG00000204120 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs768919043 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14001433 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_358619,RMVar_hsa_circ_104270,RMVar_hsa_circ_46578,RMVar_hsa_circ_38430,RMVar_hsa_circ_308150,RMVar_hsa_circ_207656,RMVar_hsa_circ_350608,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 40044 RMVar_ID_40044 Human_SNP_ID_116987773 A-to-I Human chr2 + 232727034 232727034 232727034 TTGCCCAGGCTGGAGTGCAGTGGCACGATGTCAGCTCACTGTAGCCTCTGCCTCCAGGGATCAAA TTGCCCAGGCTGGAGTGCAGTGGCACGATGTCCGCTCACTGTAGCCTCTGCCTCCAGGGATCAAA A C GIGYF2 Ensembl:ENSG00000204120 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs955374892 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_358619,RMVar_hsa_circ_104270,RMVar_hsa_circ_46578,RMVar_hsa_circ_38430,RMVar_hsa_circ_308150,RMVar_hsa_circ_207656,RMVar_hsa_circ_350608,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 40045 RMVar_ID_40045 Human_SNP_ID_116987774 A-to-I Human chr2 + 232727034 232727034 232727034 TTGCCCAGGCTGGAGTGCAGTGGCACGATGTCAGCTCACTGTAGCCTCTGCCTCCAGGGATCAAA TTGCCCAGGCTGGAGTGCAGTGGCACGATGTCGGCTCACTGTAGCCTCTGCCTCCAGGGATCAAA A G GIGYF2 Ensembl:ENSG00000204120 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs955374892 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_358619,RMVar_hsa_circ_104270,RMVar_hsa_circ_46578,RMVar_hsa_circ_38430,RMVar_hsa_circ_308150,RMVar_hsa_circ_207656,RMVar_hsa_circ_350608,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 40046 RMVar_ID_40046 Human_SNP_ID_116987782 A-to-I Human chr2 + 232727065 232727065 232727065 CAGCTCACTGTAGCCTCTGCCTCCAGGGATCAAATGATTCTCATGCCTCAGCTTCCTGAGTAACT CAGCTCACTGTAGCCTCTGCCTCCAGGGATCAGATGATTCTCATGCCTCAGCTTCCTGAGTAACT A G GIGYF2 Ensembl:ENSG00000204120 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1402502204 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_358619,RMVar_hsa_circ_104270,RMVar_hsa_circ_46578,RMVar_hsa_circ_38430,RMVar_hsa_circ_308150,RMVar_hsa_circ_207656,RMVar_hsa_circ_350608,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 40047 RMVar_ID_40047 Human_SNP_ID_116993796 A-to-I Human chr2 + 232751289 232751289 232751289 CAGGCTGTAGTGCAGTGTCACAGTCTCGGCTCACTGCAACATCTGCCTCCTGGGTTCAAGGGATT CAGGCTGTAGTGCAGTGTCACAGTCTCGGCTCGCTGCAACATCTGCCTCCTGGGTTCAAGGGATT A G GIGYF2 Ensembl:ENSG00000204120 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs532569517 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_106168,RMVar_hsa_circ_15946,RMVar_hsa_circ_207656,RMVar_hsa_circ_377989,RMVar_hsa_circ_63959,RMVar_hsa_circ_306686,RMVar_hsa_circ_49770,RMVar_hsa_circ_207658,RMVar_hsa_circ_207661,RMVar_hsa_circ_116493,RMVar_hsa_circ_304031,RMVar_hsa_circ_361789,RMVar_hsa_circ_368296,RMVar_hsa_circ_278241,RMVar_hsa_circ_314265,RMVar_hsa_circ_207663,RMVar_hsa_circ_207664,RMVar_hsa_circ_207665,RMVar_hsa_circ_378201,RMVar_hsa_circ_362368,RMVar_hsa_circ_277846,RMVar_hsa_circ_207667,RMVar_hsa_circ_207668,RMVar_hsa_circ_207666,RMVar_hsa_circ_207671 40048 RMVar_ID_40048 Human_SNP_ID_116996737 A-to-I Human chr2 + 232762839 232762827 232762839 GCCAAGGCAGGACAGCCTGGGAGACATGGTGAAACCATGTCTCTACAAAAAAGTACAAAAATTAG GCCAAGGCAGGACAGCCTGGG____________ACCATGTCTCTACAAAAAAGTACAAAAATTAG GAGACATGGTGAA G GIGYF2 Ensembl:ENSG00000204120 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1411649432 Functional Loss DEL dbSNP153 22..33 33 - - - RMVar_hsa_circ_3560,RMVar_hsa_circ_85327,RMVar_hsa_circ_207654,RMVar_hsa_circ_71108,RMVar_hsa_circ_104270,RMVar_hsa_circ_106168,RMVar_hsa_circ_15946,RMVar_hsa_circ_207656,RMVar_hsa_circ_377989,RMVar_hsa_circ_63959,RMVar_hsa_circ_49770,RMVar_hsa_circ_207661,RMVar_hsa_circ_116493,RMVar_hsa_circ_304031,RMVar_hsa_circ_361789,RMVar_hsa_circ_207665,RMVar_hsa_circ_378201,RMVar_hsa_circ_362368,RMVar_hsa_circ_207666,RMVar_hsa_circ_98662,RMVar_hsa_circ_75982,RMVar_hsa_circ_207671,RMVar_hsa_circ_14281,RMVar_hsa_circ_207672,RMVar_hsa_circ_207673 40049 RMVar_ID_40049 Human_SNP_ID_117006319 A-to-I Human chr2 + 232801094 232801094 232801094 TTAAAAAGAAAAAAAAGAGACAAATTCTTGCTATGTTGACCAGGCTGGTTTTGAACTCCTGGCCG TTAAAAAGAAAAAAAAGAGACAAATTCTTGCTGTGTTGACCAGGCTGGTTTTGAACTCCTGGCCG A G GIGYF2 Ensembl:ENSG00000204120 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs551827561 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3560,RMVar_hsa_circ_85327,RMVar_hsa_circ_207654,RMVar_hsa_circ_104270,RMVar_hsa_circ_106168,RMVar_hsa_circ_15946,RMVar_hsa_circ_207656,RMVar_hsa_circ_49770,RMVar_hsa_circ_207661,RMVar_hsa_circ_116493,RMVar_hsa_circ_98662,RMVar_hsa_circ_75982,RMVar_hsa_circ_207671,RMVar_hsa_circ_207672,RMVar_hsa_circ_353013,RMVar_hsa_circ_365156,RMVar_hsa_circ_207673,RMVar_hsa_circ_367072,RMVar_hsa_circ_362037,RMVar_hsa_circ_351333,RMVar_hsa_circ_56928,RMVar_hsa_circ_267140,RMVar_hsa_circ_68869,RMVar_hsa_circ_364881,RMVar_hsa_circ_54996,RMVar_hsa_circ_354986 40050 RMVar_ID_40050 Human_SNP_ID_117020029 A-to-I Human chr2 + 232854442 232854442 232854442 TTCAGCCTGGGAGGTGGAAGTTGCAGTGAGCCAAGATCACACCACTGCACTCCAGCCTGGGCGAC TTCAGCCTGGGAGGTGGAAGTTGCAGTGAGCCGAGATCACACCACTGCACTCCAGCCTGGGCGAC A G GIGYF2 Ensembl:ENSG00000204120 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs995244252 Functional Loss SNV dbSNP153 33..33 33 - - - 40051 RMVar_ID_40051 Human_SNP_ID_117020470 A-to-I Human chr2 + 232856060 232856060 232856060 TCAAGCAATTCTTCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGTGCCCACCACCACACCTA TCAAGCAATTCTTCTGCCTCAGCCTCCCGAGTGGCTGGGACTACAGGTGCCCACCACCACACCTA A G GIGYF2 Ensembl:ENSG00000204120 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1198743937 Functional Loss SNV dbSNP153 33..33 33 - - - 40052 RMVar_ID_40052 Human_SNP_ID_117020578 A-to-I Human chr2 + 232856488 232856488 232856488 GAGGCGGGCGGATCATTTGAGGTCAGGAGTTCAAGACCAGACTGGCCAACATGGTGAAACCCTAT GAGGCGGGCGGATCATTTGAGGTCAGGAGTTCGAGACCAGACTGGCCAACATGGTGAAACCCTAT A G GIGYF2 Ensembl:ENSG00000204120 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs565254424 Functional Loss SNV dbSNP153 33..33 33 - - - 40053 RMVar_ID_40053 Human_SNP_ID_117149557 A-to-I Human chr2 + 233337332 233337332 233337332 GCGTTCTTGGCTCACTGCAACCTCCACCTCCCAAGTTCAAGGGATTCTCCTGGCTCAGCCTCCTG GCGTTCTTGGCTCACTGCAACCTCCACCTCCCGAGTTCAAGGGATTCTCCTGGCTCAGCCTCCTG A G SAG Ensembl:ENSG00000130561 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1041333124 Functional Loss SNV dbSNP153 33..33 33 - - - 40054 RMVar_ID_40054 Human_SNP_ID_117155904 A-to-I Human chr2 + 233362441 233362441 233362441 TGGATGCTGAGGTGGGCGGATCACCTGAGGTTAGGAGTTCAAGACCAGCTTGGCCAACATGGTGA TGGATGCTGAGGTGGGCGGATCACCTGAGGTTGGGAGTTCAAGACCAGCTTGGCCAACATGGTGA A G DGKD Ensembl:ENSG00000077044 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1341826062 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109505,RMVar_hsa_circ_207719 40055 RMVar_ID_40055 Human_SNP_ID_117155944 A-to-I Human chr2 + 233362596 233362596 233362596 TCGCTTGAACCTGGGAAGTGGAAGTTGCAGTGAGCTGAGACCACACCATTACACTACAGCCTGGG TCGCTTGAACCTGGGAAGTGGAAGTTGCAGTGGGCTGAGACCACACCATTACACTACAGCCTGGG A G DGKD Ensembl:ENSG00000077044 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs750806035 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13801957 RMVar_hsa_circ_109505,RMVar_hsa_circ_207719 40056 RMVar_ID_40056 Human_SNP_ID_117167254 A-to-I Human chr2 + 233403851 233403851 233403851 TTTAGTAGAGACGGGGTTTCACCATGCTGGCCAGGCCGGTCTCGAACTCCTGACCTCGTGATCCG TTTAGTAGAGACGGGGTTTCACCATGCTGGCCGGGCCGGTCTCGAACTCCTGACCTCGTGATCCG A G DGKD Ensembl:ENSG00000077044 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs902910575 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 40057 RMVar_ID_40057 Human_SNP_ID_117167276 A-to-I Human chr2 + 233403916 233403916 233403916 CCCACCTTGGATTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCGCCCTTCCTCCCTTCAG CCCACCTTGGATTCCCAAAGTGCTGGGATTACGGGCGTGAGCCACTGCGCCCTTCCTCCCTTCAG A G DGKD Ensembl:ENSG00000077044 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1039613467 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 40058 RMVar_ID_40058 Human_SNP_ID_117168246 A-to-I Human chr2 + 233408122 233408122 233408122 TGGAGTGCCGTGCTGCGCTCTCAGCTCACTGCAACCTCCGCCTCCCGGGTTCACGCAGTTCTCCT TGGAGTGCCGTGCTGCGCTCTCAGCTCACTGCCACCTCCGCCTCCCGGGTTCACGCAGTTCTCCT A C DGKD Ensembl:ENSG00000077044 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1433192301 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 40059 RMVar_ID_40059 Human_SNP_ID_117168247 A-to-I Human chr2 + 233408122 233408122 233408122 TGGAGTGCCGTGCTGCGCTCTCAGCTCACTGCAACCTCCGCCTCCCGGGTTCACGCAGTTCTCCT TGGAGTGCCGTGCTGCGCTCTCAGCTCACTGCGACCTCCGCCTCCCGGGTTCACGCAGTTCTCCT A G DGKD Ensembl:ENSG00000077044 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1433192301 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 40060 RMVar_ID_40060 Human_SNP_ID_117571622 A-to-I Human chr2 + 234974244 234974244 234974244 AAAATTAGCCGGGCATGGTGGCGCACACCTGTAATCCCAACTACTCAGGAGGCTGAAGCAGGAGA AAAATTAGCCGGGCATGGTGGCGCACACCTGTGATCCCAACTACTCAGGAGGCTGAAGCAGGAGA A G SH3BP4 Ensembl:ENSG00000130147 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs529233451 Functional Loss SNV dbSNP153 33..33 33 - - - 40061 RMVar_ID_40061 Human_SNP_ID_117714341 A-to-I Human chr2 + 235517790 235517790 235517790 GAAACCCCGTTTCTACTAAAAATACAAAAATTAGTCAGACATGGTGGCGTGTGCCTGTAACCCCA GAAACCCCGTTTCTACTAAAAATACAAAAATTGGTCAGACATGGTGGCGTGTGCCTGTAACCCCA A G AGAP1 Ensembl:ENSG00000157985 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1396395132 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98432,RMVar_hsa_circ_207760 40062 RMVar_ID_40062 Human_SNP_ID_117714351 A-to-I Human chr2 + 235517822 235517822 235517822 AGTCAGACATGGTGGCGTGTGCCTGTAACCCCAGCTACACGGGAGGCTGAGGCAGGAGAATCTCT AGTCAGACATGGTGGCGTGTGCCTGTAACCCCGGCTACACGGGAGGCTGAGGCAGGAGAATCTCT A G AGAP1 Ensembl:ENSG00000157985 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs758330803 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98432,RMVar_hsa_circ_207760 40063 RMVar_ID_40063 Human_SNP_ID_117714950 A-to-I Human chr2 + 235520016 235520016 235520016 CATGTCCAGGCTGGTTTCGAACTACTGACCTCAGGTGATTCGCCTGCCTCGGCCTCCCAATGTGC CATGTCCAGGCTGGTTTCGAACTACTGACCTCGGGTGATTCGCCTGCCTCGGCCTCCCAATGTGC A G AGAP1 Ensembl:ENSG00000157985 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1045557252 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98432,RMVar_hsa_circ_207760 40064 RMVar_ID_40064 Human_SNP_ID_117733829 A-to-I Human chr2 + 235588109 235588109 235588109 AAAATCAGTCGGGCATGGTGGCACATGCCTGTAGTCCCAGCTACTCGGGAGACTGAGGCGGGAGA AAAATCAGTCGGGCATGGTGGCACATGCCTGTTGTCCCAGCTACTCGGGAGACTGAGGCGGGAGA A T AGAP1 Ensembl:ENSG00000157985 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1447635850 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98432,RMVar_hsa_circ_107898,RMVar_hsa_circ_207760,RMVar_hsa_circ_207762 40065 RMVar_ID_40065 Human_SNP_ID_117744788 A-to-I Human chr2 + 235627324 235627324 235627324 AAGCAATTCTGCAACCTCTACCTCCCGAGTTTAAGCAATTCTCCTGCCTCGGCCTCCTGAGTAGC AAGCAATTCTGCAACCTCTACCTCCCGAGTTTGAGCAATTCTCCTGCCTCGGCCTCCTGAGTAGC A G AGAP1 Ensembl:ENSG00000157985 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1266490216 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98432,RMVar_hsa_circ_207760 40066 RMVar_ID_40066 Human_SNP_ID_117745455 A-to-I Human chr2 + 235629687 235629687 235629687 GCCCAAGAGTTTAAGACCAGCCCTGGCAACATAGTAAGACCCTATCTCTACAATAAATGTAAAAA GCCCAAGAGTTTAAGACCAGCCCTGGCAACATGGTAAGACCCTATCTCTACAATAAATGTAAAAA A G AGAP1 Ensembl:ENSG00000157985 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1302736686 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98432,RMVar_hsa_circ_207760 40067 RMVar_ID_40067 Human_SNP_ID_117750895 A-to-I Human chr2 + 235649405 235649401 235649405 ATTGTTTTACTTTTATTTAAAGACAGATTCTCACTCTACTGCTCAGGCTGGGGTGTAGTGGTATG ATTGTTTTACTTTTATTTAAAGACAGATT____CTCTACTGCTCAGGCTGGGGTGTAGTGGTATG TCTCA T AGAP1 Ensembl:ENSG00000157985 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1297746323 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_13805727 RMVar_hsa_circ_98432,RMVar_hsa_circ_207760 40068 RMVar_ID_40068 Human_SNP_ID_117781212 A-to-I Human chr2 + 235752447 235752447 235752447 GCAATCTGCCCACCTTGGCCTCCCAAAGTGCTAGGATTATAGGCATGAGCCACCGCGCCTGGCTG GCAATCTGCCCACCTTGGCCTCCCAAAGTGCTGGGATTATAGGCATGAGCCACCGCGCCTGGCTG A G AGAP1 Ensembl:ENSG00000157985 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1196637997 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98432,RMVar_hsa_circ_207760,RMVar_hsa_circ_330369,RMVar_hsa_circ_322632,RMVar_hsa_circ_44106,RMVar_hsa_circ_29046,RMVar_hsa_circ_28906,RMVar_hsa_circ_207763,RMVar_hsa_circ_91320,RMVar_hsa_circ_17639,RMVar_hsa_circ_207768,RMVar_hsa_circ_310830,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_376280,RMVar_hsa_circ_327389,RMVar_hsa_circ_98943,RMVar_hsa_circ_102536,RMVar_hsa_circ_207777,RMVar_hsa_circ_207778,RMVar_hsa_circ_207774,RMVar_hsa_circ_207775,RMVar_hsa_circ_207773 40069 RMVar_ID_40069 Human_SNP_ID_117783691 A-to-I Human chr2 + 235760609 235760609 235760609 CTTTCTTTTTATTATTATTTCTTAATTGAGACAGGATCTCGATCTGTCACACAGGCTGGAGTACA CTTTCTTTTTATTATTATTTCTTAATTGAGACTGGATCTCGATCTGTCACACAGGCTGGAGTACA A T AGAP1 Ensembl:ENSG00000157985 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1185476052 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17570262,Human_RBP_ID_22597319 RMVar_hsa_circ_98432,RMVar_hsa_circ_207760,RMVar_hsa_circ_330369,RMVar_hsa_circ_322632,RMVar_hsa_circ_44106,RMVar_hsa_circ_29046,RMVar_hsa_circ_28906,RMVar_hsa_circ_207763,RMVar_hsa_circ_91320,RMVar_hsa_circ_17639,RMVar_hsa_circ_207768,RMVar_hsa_circ_310830,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_376280,RMVar_hsa_circ_327389,RMVar_hsa_circ_98943,RMVar_hsa_circ_102536,RMVar_hsa_circ_207777,RMVar_hsa_circ_207778,RMVar_hsa_circ_207774,RMVar_hsa_circ_207775,RMVar_hsa_circ_207773 40070 RMVar_ID_40070 Human_SNP_ID_117835420 A-to-I Human chr2 + 235943449 235943412 235943449 CAGTGGCACGATCTTGGCTCACTCTGAGGTTCAAGTAATTCTCCTGCCTCAGCCTCCCTAGTAGC _________________________________AGTAATTCTCCTGCCTCAGCCTCCCTAGTAGC GAGTGCAGTGGCACGATCTTGGCTCACTCTGAGGTTCA G AGAP1 Ensembl:ENSG00000157985 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1182899519 Functional Loss DEL dbSNP153 1..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 40071 RMVar_ID_40071 Human_SNP_ID_118140510 A-to-I Human chr2 + 237106338 237106338 237106338 TAGTTAACAAAACATATTGCATAGTTTCAGATAGCTAGAAGGAGTTTATTAAATGTTCCCAATAC TAGTTAACAAAACATATTGCATAGTTTCAGATGGCTAGAAGGAGTTTATTAAATGTTCCCAATAC A G - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs906904217 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23859136 40072 RMVar_ID_40072 Human_SNP_ID_118254923 A-to-I Human chr2 + 237552194 237552194 237552194 TTTGCATGACAGCTGAAATGTAAATACTTTTTAAAAAATATGTGATGTGGAAGCTTCTTAAAAGG TTTGCATGACAGCTGAAATGTAAATACTTTTTTAAAAATATGTGATGTGGAAGCTTCTTAAAAGG A T MLPH Ensembl:ENSG00000115648 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs73999119 Functional Loss SNV dbSNP153 33..33 33 - - - 40073 RMVar_ID_40073 Human_SNP_ID_118254924 A-to-I Human chr2 + 237552196 237552196 237552196 TGCATGACAGCTGAAATGTAAATACTTTTTAAAAAATATGTGATGTGGAAGCTTCTTAAAAGGGG TGCATGACAGCTGAAATGTAAATACTTTTTAATAAATATGTGATGTGGAAGCTTCTTAAAAGGGG A T MLPH Ensembl:ENSG00000115648 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1388272605 Functional Loss SNV dbSNP153 33..33 33 - - - 40074 RMVar_ID_40074 Human_SNP_ID_118263861 A-to-I Human chr2 - 237581146 237581146 237581146 GAGCTAGATTGATCTTCCCTCCTTGGCCTCCCAAAATGCTGGGGTTACAGGCATGAGCCACTGTA GAGCTAGATTGATCTTCCCTCCTTGGCCTCCCCAAATGCTGGGGTTACAGGCATGAGCCACTGTA T G RAB17 Ensembl:ENSG00000124839 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1307108988 Functional Loss SNV dbSNP153 33..33 33 - - - 40075 RMVar_ID_40075 Human_SNP_ID_118263867 A-to-I Human chr2 - 237581177 237581177 237581177 AGAGACAAGGTTTCACTGATCTTAAGCTCCTGAGCTAGATTGATCTTCCCTCCTTGGCCTCCCAA AGAGACAAGGTTTCACTGATCTTAAGCTCCTGGGCTAGATTGATCTTCCCTCCTTGGCCTCCCAA T C RAB17 Ensembl:ENSG00000124839 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910632258 Functional Loss SNV dbSNP153 33..33 33 - - - 40076 RMVar_ID_40076 Human_SNP_ID_118296946 A-to-I Human chr2 + 237710967 237710967 237710967 CCTGTAGTCCCAGCTACTCAGGACACTGAGGCAGGAGCATTGCTTGAGCCCAGGAGCCTGAAGCA CCTGTAGTCCCAGCTACTCAGGACACTGAGGCGGGAGCATTGCTTGAGCCCAGGAGCCTGAAGCA A G LRRFIP1 Ensembl:ENSG00000124831 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs764352435 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_207831,RMVar_hsa_circ_64623,RMVar_hsa_circ_207830,RMVar_hsa_circ_127804,RMVar_hsa_circ_297238,RMVar_hsa_circ_338703,RMVar_hsa_circ_207832 40077 RMVar_ID_40077 Human_SNP_ID_118311198 A-to-I Human chr2 + 237765127 237765127 237765127 CTACTAAAAATACAAAAAATTGGCCGGGCGTGATGGTGGGCGCCTGTAATCCCAGCCACTCCAGA CTACTAAAAATACAAAAAATTGGCCGGGCGTGGTGGTGGGCGCCTGTAATCCCAGCCACTCCAGA A G LRRFIP1 Ensembl:ENSG00000124831 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1366510375 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_546338 RMVar_hsa_circ_6644,RMVar_hsa_circ_38724,RMVar_hsa_circ_326720,RMVar_hsa_circ_207834,RMVar_hsa_circ_24892,RMVar_hsa_circ_26674 40078 RMVar_ID_40078 Human_SNP_ID_118316928 A-to-I Human chr2 + 237788169 237788169 237788169 ACGGCTCACTGCAGCCTCGACCTCTGGGGCTCAGGTGATCCTCCCCCCTCAGCCTCCAGAGTAGC ACGGCTCACTGCAGCCTCGACCTCTGGGGCTCCGGTGATCCTCCCCCCTCAGCCTCCAGAGTAGC A C LRRFIP1 Ensembl:ENSG00000124831 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1472657380 Functional Loss SNV dbSNP153 33..33 33 - - - 40079 RMVar_ID_40079 Human_SNP_ID_118383305 A-to-I Human chr2 + 238055264 238055264 238055264 TTAAAAATTACAGGCCGGGCTCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGC TTAAAAATTACAGGCCGGGCTCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGC A G UBE2F-SCLY Ensembl:ENSG00000258984 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1048930051 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_207855,RMVar_hsa_circ_207856 40080 RMVar_ID_40080 Human_SNP_ID_118387235 A-to-I Human chr2 + 238070595 238070595 238070595 CCAGCTTCTGGGGAGGTTGAGGCAGGAGAATCACTTGGATCCTGGAGATGGAGATTGCTGTGAGC CCAGCTTCTGGGGAGGTTGAGGCAGGAGAATCGCTTGGATCCTGGAGATGGAGATTGCTGTGAGC A G SCLY,UBE2F-SCLY Ensembl:ENSG00000132330,Ensembl:ENSG00000258984 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1181500938 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13810142 RMVar_hsa_circ_2844,RMVar_hsa_circ_207857,RMVar_hsa_circ_43868,RMVar_hsa_circ_120276,RMVar_hsa_circ_55768,RMVar_hsa_circ_10844 40081 RMVar_ID_40081 Human_SNP_ID_118387333 A-to-I Human chr2 + 238071004 238071004 238071004 CAGGCACACGCCACCATGCCCGGCTGATTTTTATATTTTTAAGAGAGATGGGGTTTCACCATGTT CAGGCACACGCCACCATGCCCGGCTGATTTTTGTATTTTTAAGAGAGATGGGGTTTCACCATGTT A G SCLY,UBE2F-SCLY Ensembl:ENSG00000132330,Ensembl:ENSG00000258984 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1347229730 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2844,RMVar_hsa_circ_207857,RMVar_hsa_circ_43868,RMVar_hsa_circ_120276,RMVar_hsa_circ_55768,RMVar_hsa_circ_10844 40082 RMVar_ID_40082 Human_SNP_ID_118387441 A-to-I Human chr2 + 238071486 238071475 238071486 AAAAATTTAGCCGGGCGTGGTGGTGGGCACCTATAATCCCGGCTACTCGGGAGGCTAAGGAGGAG AAAAATTTAGCCGGGCGTGGTG___________TAATCCCGGCTACTCGGGAGGCTAAGGAGGAG GGTGGGCACCTA G SCLY,UBE2F-SCLY Ensembl:ENSG00000132330,Ensembl:ENSG00000258984 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs147010911 Functional Loss DEL dbSNP153 23..33 33 - - - Human_RBP_ID_25587136 RMVar_hsa_circ_2844,RMVar_hsa_circ_207857,RMVar_hsa_circ_43868,RMVar_hsa_circ_120276,RMVar_hsa_circ_55768,RMVar_hsa_circ_10844 40083 RMVar_ID_40083 Human_SNP_ID_118387447 A-to-I Human chr2 + 238071486 238071486 238071486 AAAAATTTAGCCGGGCGTGGTGGTGGGCACCTATAATCCCGGCTACTCGGGAGGCTAAGGAGGAG AAAAATTTAGCCGGGCGTGGTGGTGGGCACCTGTAATCCCGGCTACTCGGGAGGCTAAGGAGGAG A G SCLY,UBE2F-SCLY Ensembl:ENSG00000132330,Ensembl:ENSG00000258984 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1478475569 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25587136 RMVar_hsa_circ_2844,RMVar_hsa_circ_207857,RMVar_hsa_circ_43868,RMVar_hsa_circ_120276,RMVar_hsa_circ_55768,RMVar_hsa_circ_10844 40084 RMVar_ID_40084 Human_SNP_ID_118387455 A-to-I Human chr2 + 238071537 238071537 238071537 AGGCTAAGGAGGAGAAGAATCACTTGAACCTGAGAGGGAGAGGTTGCAGTGAGCCAAAATCGTGC AGGCTAAGGAGGAGAAGAATCACTTGAACCTGGGAGGGAGAGGTTGCAGTGAGCCAAAATCGTGC A G SCLY,UBE2F-SCLY Ensembl:ENSG00000132330,Ensembl:ENSG00000258984 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1055585310 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2844,RMVar_hsa_circ_207857,RMVar_hsa_circ_43868,RMVar_hsa_circ_120276,RMVar_hsa_circ_55768,RMVar_hsa_circ_10844 40085 RMVar_ID_40085 Human_SNP_ID_118387974 A-to-I Human chr2 + 238074221 238074221 238074221 CCAGCTACTTGGGAGGCTGAGGCAGGAGAATCACTTGAACCCGGAAGGCGGAGGCTGTAGTGAAC CCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGGAAGGCGGAGGCTGTAGTGAAC A G SCLY,UBE2F-SCLY Ensembl:ENSG00000132330,Ensembl:ENSG00000258984 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs983331259 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2844,RMVar_hsa_circ_207857,RMVar_hsa_circ_43868,RMVar_hsa_circ_120276,RMVar_hsa_circ_55768 40086 RMVar_ID_40086 Human_SNP_ID_118387975 A-to-I Human chr2 + 238074221 238074221 238074221 CCAGCTACTTGGGAGGCTGAGGCAGGAGAATCACTTGAACCCGGAAGGCGGAGGCTGTAGTGAAC CCAGCTACTTGGGAGGCTGAGGCAGGAGAATCTCTTGAACCCGGAAGGCGGAGGCTGTAGTGAAC A T SCLY,UBE2F-SCLY Ensembl:ENSG00000132330,Ensembl:ENSG00000258984 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs983331259 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2844,RMVar_hsa_circ_207857,RMVar_hsa_circ_43868,RMVar_hsa_circ_120276,RMVar_hsa_circ_55768 40087 RMVar_ID_40087 Human_SNP_ID_118393199 A-to-I Human chr2 + 238094947 238094947 238094947 GGCAGAGGCTGGGCACAGTGGCTCGTGCCTGTAATCCTAGCACTTTTGGAGGCTGAGGCAGGCTG GGCAGAGGCTGGGCACAGTGGCTCGTGCCTGTGATCCTAGCACTTTTGGAGGCTGAGGCAGGCTG A G SCLY,UBE2F-SCLY Ensembl:ENSG00000132330,Ensembl:ENSG00000258984 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs986557237 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99518,RMVar_hsa_circ_207860,RMVar_hsa_circ_354358 40088 RMVar_ID_40088 Human_SNP_ID_118393215 A-to-I Human chr2 + 238095014 238095014 238095014 CACAAGGTCAAGAGATTGAGTCCAGCCTGGCCAACATGGAGAAACCCCATCTCTACCAAAAACTA CACAAGGTCAAGAGATTGAGTCCAGCCTGGCCGACATGGAGAAACCCCATCTCTACCAAAAACTA A G SCLY,UBE2F-SCLY Ensembl:ENSG00000132330,Ensembl:ENSG00000258984 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs573760717 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99518,RMVar_hsa_circ_207860,RMVar_hsa_circ_354358 40089 RMVar_ID_40089 Human_SNP_ID_118393235 A-to-I Human chr2 + 238095082 238095082 238095082 AAAATTAGCCAGGCATAGTGGTGTGCACCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA AAAATTAGCCAGGCATAGTGGTGTGCACCTGTGGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA A G SCLY,UBE2F-SCLY Ensembl:ENSG00000132330,Ensembl:ENSG00000258984 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1022576461 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99518,RMVar_hsa_circ_207860,RMVar_hsa_circ_354358 40090 RMVar_ID_40090 Human_SNP_ID_118393403 A-to-I Human chr2 + 238095769 238095769 238095769 TTTTATTTATTTATTTTTTGATTCAGGGTCTCACTCTGTCGTCACCCAGGCTGGAGTGCTGTGGC TTTTATTTATTTATTTTTTGATTCAGGGTCTCGCTCTGTCGTCACCCAGGCTGGAGTGCTGTGGC A G SCLY,UBE2F-SCLY Ensembl:ENSG00000132330,Ensembl:ENSG00000258984 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs918190430 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13810512 RMVar_hsa_circ_99518,RMVar_hsa_circ_207860,RMVar_hsa_circ_354358 40091 RMVar_ID_40091 Human_SNP_ID_118393522 A-to-I Human chr2 + 238096241 238096241 238096241 TGGCTAATTTTTAAAAAATATTTTGTAGAGATAGGGTTTCCCTGTGTTGCCCAGGCTGGTCTCAA TGGCTAATTTTTAAAAAATATTTTGTAGAGATGGGGTTTCCCTGTGTTGCCCAGGCTGGTCTCAA A G SCLY,UBE2F-SCLY Ensembl:ENSG00000132330,Ensembl:ENSG00000258984 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1420194341 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99518,RMVar_hsa_circ_207860,RMVar_hsa_circ_354358 40092 RMVar_ID_40092 Human_SNP_ID_118423126 A-to-I Human chr2 - 238191742 238191742 238191742 ACCATGCCCGGCTAATTTTTTGTATTTTAATTAGAGACCGGGTTTCGCCATGTTGGTCAGGCTTG ACCATGCCCGGCTAATTTTTTGTATTTTAATTGGAGACCGGGTTTCGCCATGTTGGTCAGGCTTG T C ILKAP Ensembl:ENSG00000132323 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs771929454 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102288,RMVar_hsa_circ_110884,RMVar_hsa_circ_207863,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_207877,RMVar_hsa_circ_376764,RMVar_hsa_circ_50184,RMVar_hsa_circ_289457,RMVar_hsa_circ_207886,RMVar_hsa_circ_21027 40093 RMVar_ID_40093 Human_SNP_ID_118424306 A-to-I Human chr2 - 238195821 238195821 238195821 CCAGGCTGGTCTCGAACTCCGGGACTCAAGCAATCCTCCCACCTCAGCCTACCGAAGTGCTGGGT CCAGGCTGGTCTCGAACTCCGGGACTCAAGCAGTCCTCCCACCTCAGCCTACCGAAGTGCTGGGT T C ILKAP Ensembl:ENSG00000132323 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1365995755 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13811542 RMVar_hsa_circ_207876,RMVar_hsa_circ_85776 40094 RMVar_ID_40094 Human_SNP_ID_118424327 A-to-I Human chr2 - 238195903 238195903 238195903 GAGTAGCTTGGACTACAGGCGCCTGCCACCACACCTGGCTAATTTTTGTATTTTTTTCATAGACA GAGTAGCTTGGACTACAGGCGCCTGCCACCACGCCTGGCTAATTTTTGTATTTTTTTCATAGACA T C ILKAP Ensembl:ENSG00000132323 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1179136699 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_207876,RMVar_hsa_circ_85776 40095 RMVar_ID_40095 Human_SNP_ID_118424343 A-to-I Human chr2 - 238195948 238195948 238195948 CCTTGGCCTCCCTGGGCTCAGGTGATCCTCCCACCTCAGCCTACTGAGTAGCTTGGACTACAGGC CCTTGGCCTCCCTGGGCTCAGGTGATCCTCCCGCCTCAGCCTACTGAGTAGCTTGGACTACAGGC T C ILKAP Ensembl:ENSG00000132323 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs368692026 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_207876,RMVar_hsa_circ_85776 40096 RMVar_ID_40096 Human_SNP_ID_118424345 A-to-I Human chr2 - 238195961 238195957 238195962 TGGCTCACTGAAGCCTTGGCCTCCCTGGGCTCAGGTGATCCTCCCACCTCAGCCTACTGAGTAGC TGGCTCACTGAAGCCTTGGCCTCCCTGGGCT_____GATCCTCCCACCTCAGCCTACTGAGTAGC CACCTG C ILKAP Ensembl:ENSG00000132323 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1292417510 Functional Loss DEL dbSNP153 32..36 33 - - - RMVar_hsa_circ_207876,RMVar_hsa_circ_85776 40097 RMVar_ID_40097 Human_SNP_ID_118424347 A-to-I Human chr2 - 238195961 238195961 238195961 TGGCTCACTGAAGCCTTGGCCTCCCTGGGCTCAGGTGATCCTCCCACCTCAGCCTACTGAGTAGC TGGCTCACTGAAGCCTTGGCCTCCCTGGGCTCGGGTGATCCTCCCACCTCAGCCTACTGAGTAGC T C ILKAP Ensembl:ENSG00000132323 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs578097097 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_207876,RMVar_hsa_circ_85776 40098 RMVar_ID_40098 Human_SNP_ID_118474885 A-to-I Human chr2 + 238386361 238386361 238386361 TTGTGACAGAGTCTCACTCTGTCTCCCAGGCTAGCGTGCAGTGGTGTGATTTTGGCTCACTGCAA TTGTGACAGAGTCTCACTCTGTCTCCCAGGCTGGCGTGCAGTGGTGTGATTTTGGCTCACTGCAA A G TRAF3IP1 Ensembl:ENSG00000204104 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs550713716 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_148088 40099 RMVar_ID_40099 Human_SNP_ID_118892113 A-to-I Human chr2 - 239932718 239932718 239932718 AAAATTAGCCGGGTATGGTGGCGGATGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTAGCCGGGTATGGTGGCGGATGCCTGTGGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA T C NDUFA10 Ensembl:ENSG00000130414 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1199031889 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67450 40100 RMVar_ID_40100 Human_SNP_ID_697844865 A-to-I Human chr22 + 15811320 15811320 15811320 CTTTGAGGTATATAGCCCCAATAATTAAATGCAGGGACCCAAAAAGATATTTGCATAGCAATGTT CTTTGAGGTATATAGCCCCAATAATTAAATGCGGGGACCCAAAAAGATATTTGCATAGCAATGTT A G DUXAP8 Ensembl:ENSG00000206195 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs4490286 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2711469 40101 RMVar_ID_40101 Human_SNP_ID_698214966 A-to-I Human chr22 + 17052799 17052799 17052799 GCCATGAAGCCCAGCTAATTTTTTGTATTTTTAGTACAGACAGGGTTTCACCATGTTAGCCAGGC GCCATGAAGCCCAGCTAATTTTTTGTATTTTTGGTACAGACAGGGTTTCACCATGTTAGCCAGGC A G CECR7 Ensembl:ENSG00000237438 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1248735594 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89516,RMVar_hsa_circ_212811 40102 RMVar_ID_40102 Human_SNP_ID_698218190 A-to-I Human chr22 + 17066029 17066029 17066029 TAAAAAATTATTGGATGTGGTGGTGCATGCCTATAGTCCCAGCTACTTGGGAGGCTGAGGCAGGA TAAAAAATTATTGGATGTGGTGGTGCATGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1159352127 Functional Loss SNV dbSNP153 33..33 33 - - - 40103 RMVar_ID_40103 Human_SNP_ID_698219181 A-to-I Human chr22 + 17068986 17068986 17068986 TAATTTATTTATTTATTTTGAGACGGAGTCTTACTCTGCTGCTCAGGCTGGAGTGCAGTGGCATG TAATTTATTTATTTATTTTGAGACGGAGTCTTCCTCTGCTGCTCAGGCTGGAGTGCAGTGGCATG A C AC006946.2 Ensembl:ENSG00000273203 lincRNA exon GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1372760306 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22604027 40104 RMVar_ID_40104 Human_SNP_ID_698220526 A-to-I Human chr22 + 17075326 17075326 17075326 AGCTGGGCGTGGTGACACGCGCCTGTAGTCCCAGCTACTCGGCAGGCTGAGGCAGGGGAATCGCT AGCTGGGCGTGGTGACACGCGCCTGTAGTCCCTGCTACTCGGCAGGCTGAGGCAGGGGAATCGCT A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1428813488 Functional Loss SNV dbSNP153 33..33 33 - - - 40105 RMVar_ID_40105 Human_SNP_ID_698230449 A-to-I Human chr22 + 17110551 17110551 17110551 TGGTCACGCGGGATGTAAACGCTGAATGGGCCAGGTGCAGTGGCTCATGCTTGTAATCCCAGCAC TGGTCACGCGGGATGTAAACGCTGAATGGGCCTGGTGCAGTGGCTCATGCTTGTAATCCCAGCAC A T IL17RA Ensembl:ENSG00000177663 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1342917933 Functional Loss SNV dbSNP153 33..33 33 - - - 40106 RMVar_ID_40106 Human_SNP_ID_698232192 A-to-I Human chr22 - 17117537 17117537 17117537 TGCAGAGTGCACAGGGAGGGTCAGAAGTGCCAAGTCACTGGCCGTTAACTCAGCACCCAGGCCAA TGCAGAGTGCACAGGGAGGGTCAGAAGTGCCATGTCACTGGCCGTTAACTCAGCACCCAGGCCAA T A TMEM121B Ensembl:ENSG00000183307 Protein coding 3'UTR GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs532427550 Functional Loss SNV dbSNP153 33..33 33 - - - 40107 RMVar_ID_40107 Human_SNP_ID_698232193 A-to-I Human chr22 - 17117537 17117537 17117537 TGCAGAGTGCACAGGGAGGGTCAGAAGTGCCAAGTCACTGGCCGTTAACTCAGCACCCAGGCCAA TGCAGAGTGCACAGGGAGGGTCAGAAGTGCCACGTCACTGGCCGTTAACTCAGCACCCAGGCCAA T G TMEM121B Ensembl:ENSG00000183307 Protein coding 3'UTR GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs532427550 Functional Loss SNV dbSNP153 33..33 33 - - - 40108 RMVar_ID_40108 Human_SNP_ID_698240983 A-to-I Human chr22 - 17150065 17150065 17150065 CACGCCTAATAATCCTAGCATTAAATTTAGGAAGCTGAGGCGAGAGGATCCCTTGAGCCCAGTGG CACGCCTAATAATCCTAGCATTAAATTTAGGAGGCTGAGGCGAGAGGATCCCTTGAGCCCAGTGG T C HDHD5 Ensembl:ENSG00000069998 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1434718913 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14383193 40109 RMVar_ID_40109 Human_SNP_ID_698241335 A-to-I Human chr22 - 17151647 17151647 17151647 CGGCTCACTGCATCCTCTGCCTCCCAGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCT CGGCTCACTGCATCCTCTGCCTCCCAGGTTCAGGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCT T C HDHD5 Ensembl:ENSG00000069998 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264985454 Functional Loss SNV dbSNP153 33..33 33 - - - 40110 RMVar_ID_40110 Human_SNP_ID_698363901 A-to-I Human chr22 - 17595649 17595649 17595649 GCCCAGCTAATTTTTGTATTTTTAGTGGAGACAGGCTTTCGCCATGTTGGCCAGGCTGGCCTCAA GCCCAGCTAATTTTTGTATTTTTAGTGGAGACGGGCTTTCGCCATGTTGGCCAGGCTGGCCTCAA T C ATP6V1E1 Ensembl:ENSG00000131100 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1460854526 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_304204,RMVar_hsa_circ_338385 40111 RMVar_ID_40111 Human_SNP_ID_698363918 A-to-I Human chr22 - 17595734 17595734 17595734 TTGCTGCAACCTCTGCCTCCTGGGTTCAAGCAATTCTCCTGCCTCAGTCTCTCAAGTAGCTGGGA TTGCTGCAACCTCTGCCTCCTGGGTTCAAGCAGTTCTCCTGCCTCAGTCTCTCAAGTAGCTGGGA T C ATP6V1E1 Ensembl:ENSG00000131100 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1002835180 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_304204,RMVar_hsa_circ_338385 40112 RMVar_ID_40112 Human_SNP_ID_698364501 A-to-I Human chr22 - 17597813 17597813 17597813 CCACCCTCTGCTCATAGTCCAGTCCTGTCTCTACTAAAAATACAAAAATTAGCTGAGCGTGGTGG CCACCCTCTGCTCATAGTCCAGTCCTGTCTCTGCTAAAAATACAAAAATTAGCTGAGCGTGGTGG T C ATP6V1E1 Ensembl:ENSG00000131100 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1439848601 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_304204,RMVar_hsa_circ_338385 40113 RMVar_ID_40113 Human_SNP_ID_698364523 A-to-I Human chr22 - 17597912 17597912 17597912 AACACTTTGGGAGGCTGAGGCAGGTGGATCACAAGGTCAAGAGATCGAGACCATCCTTACCAACA AACACTTTGGGAGGCTGAGGCAGGTGGATCACCAGGTCAAGAGATCGAGACCATCCTTACCAACA T G ATP6V1E1 Ensembl:ENSG00000131100 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1051301022 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_304204,RMVar_hsa_circ_338385 40114 RMVar_ID_40114 Human_SNP_ID_698366456 A-to-I Human chr22 - 17605153 17605153 17605153 TCCCCCAGGCTGGAGTGCAATGGCGTGATCTCAACTCACTGCAGCCTCCGCCACCCGGGTTCAAG TCCCCCAGGCTGGAGTGCAATGGCGTGATCTCGACTCACTGCAGCCTCCGCCACCCGGGTTCAAG T C ATP6V1E1 Ensembl:ENSG00000131100 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1169315275 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4998,RMVar_hsa_circ_60278,RMVar_hsa_circ_65656 40115 RMVar_ID_40115 Human_SNP_ID_698367851 A-to-I Human chr22 - 17610084 17610084 17610084 TGGTCTGGCTATGTTGCCCAGGCTGGAATGCAATGGTGCAGTCATAGCTCACAAACTCCTGGGCT TGGTCTGGCTATGTTGCCCAGGCTGGAATGCAGTGGTGCAGTCATAGCTCACAAACTCCTGGGCT T C ATP6V1E1 Ensembl:ENSG00000131100 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs981891357 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4998,RMVar_hsa_circ_60278,RMVar_hsa_circ_65656 40116 RMVar_ID_40116 Human_SNP_ID_698372794 A-to-I Human chr22 - 17627653 17627653 17627653 CAAGCCCGGCTAATTTTTGTATTTTTTTTAGTAGAGGCAGGGTCTCACCATATTGGCCTGGCTGG CAAGCCCGGCTAATTTTTGTATTTTTTTTAGTGGAGGCAGGGTCTCACCATATTGGCCTGGCTGG T C ATP6V1E1 Ensembl:ENSG00000131100 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1338407761 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14384805 40117 RMVar_ID_40117 Human_SNP_ID_698378612 A-to-I Human chr22 + 17646739 17646739 17646739 AATATCTGTCTTTTTTTTTTTTTTTTTTTTTGAGATAGAGTCTAGCTCTGTCGCCTAGGCTGGAG AATATCTGTCTTTTTTTTTTTTTTTTTTTTTGTGATAGAGTCTAGCTCTGTCGCCTAGGCTGGAG A T BCL2L13 Ensembl:ENSG00000099968 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1210247805 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14385082 RMVar_hsa_circ_325670 40118 RMVar_ID_40118 Human_SNP_ID_698378615 A-to-I Human chr22 + 17646743 17646743 17646743 TCTGTCTTTTTTTTTTTTTTTTTTTTTGAGATAGAGTCTAGCTCTGTCGCCTAGGCTGGAGTGCA TCTGTCTTTTTTTTTTTTTTTTTTTTTGAGATTGAGTCTAGCTCTGTCGCCTAGGCTGGAGTGCA A T BCL2L13 Ensembl:ENSG00000099968 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1407173889 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14385082 RMVar_hsa_circ_325670 40119 RMVar_ID_40119 Human_SNP_ID_698380706 A-to-I Human chr22 + 17653644 17653644 17653644 CTGCCTTATCAGCCTCCCAAGTAACTAGGACTACAGGCGCATGCCACCACACCCAGGGCTAATTT CTGCCTTATCAGCCTCCCAAGTAACTAGGACTGCAGGCGCATGCCACCACACCCAGGGCTAATTT A G BCL2L13 Ensembl:ENSG00000099968 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs957209658 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_325670 40120 RMVar_ID_40120 Human_SNP_ID_698387296 A-to-I Human chr22 + 17678213 17678213 17678213 CTCAGCTAGTTTTTTTTATTTTTCGTAGAAACAAGGTCTAGCTATGTTGCGCAGGCTGTTCTTGA CTCAGCTAGTTTTTTTTATTTTTCGTAGAAACGAGGTCTAGCTATGTTGCGCAGGCTGTTCTTGA A G BCL2L13 Ensembl:ENSG00000099968 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1363446591 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7060300 RMVar_hsa_circ_212841,RMVar_hsa_circ_291308,RMVar_hsa_circ_308990,RMVar_hsa_circ_325670,RMVar_hsa_circ_289604,RMVar_hsa_circ_212839,RMVar_hsa_circ_212840 40121 RMVar_ID_40121 Human_SNP_ID_698387765 A-to-I Human chr22 + 17680035 17680035 17680035 AGGAGTTCGAGATCAGCCTGGCCAACATGATGAAGCACCATCTCTACTAAAAATACAAAAAATTA AGGAGTTCGAGATCAGCCTGGCCAACATGATGGAGCACCATCTCTACTAAAAATACAAAAAATTA A G BCL2L13 Ensembl:ENSG00000099968 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1011456895 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_212841,RMVar_hsa_circ_291308,RMVar_hsa_circ_308990,RMVar_hsa_circ_325670,RMVar_hsa_circ_289604,RMVar_hsa_circ_212839,RMVar_hsa_circ_212840 40122 RMVar_ID_40122 Human_SNP_ID_698389764 A-to-I Human chr22 + 17686375 17686375 17686375 CGGAGGCTAAGGCATGAGAATCTCTTGAACCCAGGAAGCATAGGTTGTAGTGAGCCAAGATCATG CGGAGGCTAAGGCATGAGAATCTCTTGAACCCGGGAAGCATAGGTTGTAGTGAGCCAAGATCATG A G BCL2L13 Ensembl:ENSG00000099968 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs868523478 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_212842,RMVar_hsa_circ_212841,RMVar_hsa_circ_291308,RMVar_hsa_circ_308990,RMVar_hsa_circ_289604,RMVar_hsa_circ_212839,RMVar_hsa_circ_212840,RMVar_hsa_circ_313675,RMVar_hsa_circ_350649,RMVar_hsa_circ_270697 40123 RMVar_ID_40123 Human_SNP_ID_698391811 A-to-I Human chr22 + 17694001 17694001 17694001 GCTGATCTTGAATTCCTGACTTCAAGCGATCCACCTGCCTTGGCCTCCCAAAGTGTTGGGATTAC GCTGATCTTGAATTCCTGACTTCAAGCGATCCTCCTGCCTTGGCCTCCCAAAGTGTTGGGATTAC A T BCL2L13 Ensembl:ENSG00000099968 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404715036 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_212842,RMVar_hsa_circ_212841,RMVar_hsa_circ_291308,RMVar_hsa_circ_289604,RMVar_hsa_circ_212840,RMVar_hsa_circ_313675,RMVar_hsa_circ_270697,RMVar_hsa_circ_304637,RMVar_hsa_circ_322180,RMVar_hsa_circ_212844 40124 RMVar_ID_40124 Human_SNP_ID_698391893 A-to-I Human chr22 + 17694395 17694394 17694395 TAACACTCCAAGTTAAAAATAGGACTCCAGCTAGGGGTGGTGGGACAGGCCTGTAATCCCAGCTA TAACACTCCAAGTTAAAAATAGGACTCCAGCT_GGGGTGGTGGGACAGGCCTGTAATCCCAGCTA TA T BCL2L13 Ensembl:ENSG00000099968 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs967400426 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_212842,RMVar_hsa_circ_212841,RMVar_hsa_circ_291308,RMVar_hsa_circ_289604,RMVar_hsa_circ_212840,RMVar_hsa_circ_313675,RMVar_hsa_circ_270697,RMVar_hsa_circ_304637,RMVar_hsa_circ_322180,RMVar_hsa_circ_212844 40125 RMVar_ID_40125 Human_SNP_ID_698402805 A-to-I Human chr22 - 17735698 17735698 17735698 TGCACGGATAGGACTTCAGGGGTCTGGAGAACATGTTTTTGCATAAACCCCAGCTTTGCTCTACT TGCACGGATAGGACTTCAGGGGTCTGGAGAACGTGTTTTTGCATAAACCCCAGCTTTGCTCTACT T C BID Ensembl:ENSG00000015475 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs181382 Functional Loss SNV dbSNP153,EGP 33..33 33 - - - GWAS_ID_4724,GWAS_ID_4725,GWAS_ID_4726,GWAS_ID_4727,GWAS_ID_4728,GWAS_ID_4729,GWAS_ID_4730,GWAS_ID_4731,GWAS_ID_4732,GWAS_ID_4733,GWAS_ID_4734,GWAS_ID_4735,GWAS_ID_4736,GWAS_ID_4737,GWAS_ID_4738,GWAS_ID_4739,GWAS_ID_4740,GWAS_ID_4741,GWAS_ID_4742,GWAS_ID_4743,GWAS_ID_4744,GWAS_ID_4745,GWAS_ID_4746,GWAS_ID_4747 40126 RMVar_ID_40126 Human_SNP_ID_698405139 A-to-I Human chr22 - 17743853 17743853 17743853 GGCTCCCCAGTGGGAGGGCTACGATGAGCTGCAGACTGATGGCAACCGCAGCAGCCACTCCCGCT GGCTCCCCAGTGGGAGGGCTACGATGAGCTGCGGACTGATGGCAACCGCAGCAGCCACTCCCGCT T C BID Ensembl:ENSG00000015475 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs755629886 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4684103,Human_RBP_ID_26822155 Human_Splice_Rec_2134897,Human_Splice_Rec_2134913,Human_Splice_Rec_2134929,Human_Splice_Rec_2134939,Human_Splice_Rec_2134959,Human_Splice_Rec_2134971,Human_Splice_Rec_2134981,Human_Splice_Rec_2134995,Human_Splice_Rec_2135001,Human_Splice_Rec_2135007 RMVar_hsa_circ_15082 40127 RMVar_ID_40127 Human_SNP_ID_698405589 A-to-I Human chr22 - 17745550 17745549 17745551 AAACTTCTGGGCTCAAGTGACCTTCCCGCCTCAGTCTCATGAGTAGCTGGGACTGCAGGTGCATG AAACTTCTGGGCTCAAGTGACCTTCCCGCCT__GTCTCATGAGTAGCTGGGACTGCAGGTGCATG CTG C BID Ensembl:ENSG00000015475 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1397209498 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_15082 40128 RMVar_ID_40128 Human_SNP_ID_698405973 A-to-I Human chr22 - 17747008 17747008 17747008 AGTTTGATAACCTGACCTGCTGTGGTGGCAGCACCGCTCTGTGTCCAGATTCTGGATGCCAATTT AGTTTGATAACCTGACCTGCTGTGGTGGCAGCGCCGCTCTGTGTCCAGATTCTGGATGCCAATTT T C BID Ensembl:ENSG00000015475 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs181402 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_4748,GWAS_ID_4749,GWAS_ID_4750,GWAS_ID_4751 RMVar_hsa_circ_15082 40129 RMVar_ID_40129 Human_SNP_ID_698406204 A-to-I Human chr22 - 17747928 17747928 17747928 GGGATTGCAGGCGTGAGCCACCGCACCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCA GGGATTGCAGGCGTGAGCCACCGCACCTGGCTGATTTTTGTATTTTTAGTAGAGATGGGGTTTCA T C BID Ensembl:ENSG00000015475 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1409632155 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15082 40130 RMVar_ID_40130 Human_SNP_ID_698422261 A-to-I Human chr22 - 17802191 17802191 17802191 GGGCATAGTGGCACGTGCCTGTAGTTCCATCTACTAGGGAGGCTAAGGTGGGAGGATCACATGAG GGGCATAGTGGCACGTGCCTGTAGTTCCATCTGCTAGGGAGGCTAAGGTGGGAGGATCACATGAG T C AC016026.1,MICAL3 Ensembl:ENSG00000093100,Ensembl:ENSG00000243156 lincRNA,Protein coding intron,intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs529352108 Functional Loss SNV dbSNP153 33..33 33 - - - 40131 RMVar_ID_40131 Human_SNP_ID_698473019 A-to-I Human chr22 - 17982657 17982657 17982657 TTATGTTATGAATTTTTTTGAGATGAAGTCTTACTCTGTCGCCCAGGCTGGAGTACAGTGGTACA TTATGTTATGAATTTTTTTGAGATGAAGTCTTGCTCTGTCGCCCAGGCTGGAGTACAGTGGTACA T C MICAL3 Ensembl:ENSG00000243156 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965295262 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14387721 RMVar_hsa_circ_126825,RMVar_hsa_circ_212874,RMVar_hsa_circ_212869,RMVar_hsa_circ_103449 40132 RMVar_ID_40132 Human_SNP_ID_698476190 A-to-I Human chr22 - 17994601 17994601 17994601 CCAGGCCATCCCCCAACCTCAGCCTCCTGAGTAGCTGGGACTACAGGCCCACACCACCACACCCG CCAGGCCATCCCCCAACCTCAGCCTCCTGAGTGGCTGGGACTACAGGCCCACACCACCACACCCG T C MICAL3 Ensembl:ENSG00000243156 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1479307326 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126825,RMVar_hsa_circ_212874,RMVar_hsa_circ_212869,RMVar_hsa_circ_103449 40133 RMVar_ID_40133 Human_SNP_ID_698476225 A-to-I Human chr22 - 17994708 17994708 17994708 TTTTTTCTTTTTTTTTTTTGAGACAGAGTCTTACTCTGTGGCCCCGGCTGGAGTGGCCCCAGCTG TTTTTTCTTTTTTTTTTTTGAGACAGAGTCTTGCTCTGTGGCCCCGGCTGGAGTGGCCCCAGCTG T C MICAL3 Ensembl:ENSG00000243156 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1317650891 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14387952 RMVar_hsa_circ_126825,RMVar_hsa_circ_212874,RMVar_hsa_circ_212869,RMVar_hsa_circ_103449 40134 RMVar_ID_40134 Human_SNP_ID_698476226 A-to-I Human chr22 - 17994714 17994712 17994714 TTCTTTTTTTTTCTTTTTTTTTTTTGAGACAGAGTCTTACTCTGTGGCCCCGGCTGGAGTGGCCC TTCTTTTTTTTTCTTTTTTTTTTTTGAGACAG__TCTTACTCTGTGGCCCCGGCTGGAGTGGCCC ACT A MICAL3 Ensembl:ENSG00000243156 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1218922555 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_14387952 RMVar_hsa_circ_126825,RMVar_hsa_circ_212874,RMVar_hsa_circ_212869,RMVar_hsa_circ_103449 40135 RMVar_ID_40135 Human_SNP_ID_698476227 A-to-I Human chr22 - 17994714 17994714 17994714 TTCTTTTTTTTTCTTTTTTTTTTTTGAGACAGAGTCTTACTCTGTGGCCCCGGCTGGAGTGGCCC TTCTTTTTTTTTCTTTTTTTTTTTTGAGACAGTGTCTTACTCTGTGGCCCCGGCTGGAGTGGCCC T A MICAL3 Ensembl:ENSG00000243156 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1266993825 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14387952 RMVar_hsa_circ_126825,RMVar_hsa_circ_212874,RMVar_hsa_circ_212869,RMVar_hsa_circ_103449 40136 RMVar_ID_40136 Human_SNP_ID_698476228 A-to-I Human chr22 - 17994716 17994716 17994716 GCTTCTTTTTTTTTCTTTTTTTTTTTTGAGACAGAGTCTTACTCTGTGGCCCCGGCTGGAGTGGC GCTTCTTTTTTTTTCTTTTTTTTTTTTGAGACGGAGTCTTACTCTGTGGCCCCGGCTGGAGTGGC T C MICAL3 Ensembl:ENSG00000243156 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1326997726 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14387952 RMVar_hsa_circ_126825,RMVar_hsa_circ_212874,RMVar_hsa_circ_212869,RMVar_hsa_circ_103449 40137 RMVar_ID_40137 Human_SNP_ID_698477161 A-to-I Human chr22 - 17998195 17998194 17998195 GGTTCGAGCGATTCTTCTGCCTCAGCCTCTCAAGTAGCTGGGACTACAGGCACCTGCCACCACGC GGTTCGAGCGATTCTTCTGCCTCAGCCTCTCA_GTAGCTGGGACTACAGGCACCTGCCACCACGC CT C MICAL3 Ensembl:ENSG00000243156 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1475390913 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_126825,RMVar_hsa_circ_212874,RMVar_hsa_circ_212869,RMVar_hsa_circ_103449 40138 RMVar_ID_40138 Human_SNP_ID_698479211 A-to-I Human chr22 - 18005039 18005039 18005039 ATCTCAGCTACTTGGGAGGCTGAGGCATGAGAATCGCTTGAAATCAGGAGGCAGAGGTTGCAGTG ATCTCAGCTACTTGGGAGGCTGAGGCATGAGAGTCGCTTGAAATCAGGAGGCAGAGGTTGCAGTG T C AC016027.2,MICAL3 Ensembl:ENSG00000234913,Ensembl:ENSG00000243156 lincRNA,Protein coding exon,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1173199551 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_212874,RMVar_hsa_circ_103449 40139 RMVar_ID_40139 Human_SNP_ID_698481670 A-to-I Human chr22 - 18015654 18015654 18015654 AGGGTCGCGCGTGGTCGGAGGCCATGACAGGCAGATCACCTGAGGTCAGGAGTTCGAGATCAGCT AGGGTCGCGCGTGGTCGGAGGCCATGACAGGCGGATCACCTGAGGTCAGGAGTTCGAGATCAGCT T C MICAL3 Ensembl:ENSG00000243156 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs574982083 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_212874,RMVar_hsa_circ_103449 40140 RMVar_ID_40140 Human_SNP_ID_698500663 A-to-I Human chr22 + 18084450 18084450 18084450 TATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGGTCTCAATCTCCTGACCTCGTGA TATTTTTAGTAGAGACGGGGTTTCACCGTGTTGGCCAGGATGGTCTCAATCTCCTGACCTCGTGA A G PEX26 Ensembl:ENSG00000215193 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1039106545 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18613 40141 RMVar_ID_40141 Human_SNP_ID_698501744 A-to-I Human chr22 + 18088511 18088511 18088511 TTGAGAAACATACTTCTTTGCTGGGCATGGTGACTCACGCCTGTAATCCCAGCACTTTGGAAGGG TTGAGAAACATACTTCTTTGCTGGGCATGGTGTCTCACGCCTGTAATCCCAGCACTTTGGAAGGG A T PEX26 Ensembl:ENSG00000215193 Protein coding 3'UTR GSE47997;GSE38233;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,32596459 RNA-Seq:(High) rs936692781 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_498944,Human_miRNA_ID_1359401 RMVar_hsa_circ_93299,RMVar_hsa_circ_212879 40142 RMVar_ID_40142 Human_SNP_ID_698501752 A-to-I Human chr22 + 18088539 18088539 18088539 GGTGACTCACGCCTGTAATCCCAGCACTTTGGAAGGGTGAGGTGGGTGGATCACTTGTGGCCAGG GGTGACTCACGCCTGTAATCCCAGCACTTTGGGAGGGTGAGGTGGGTGGATCACTTGTGGCCAGG A G PEX26 Ensembl:ENSG00000215193 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs141229564 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4684391 Clinvar_Rec_118,Clinvar_Rec_119,Clinvar_Rec_120,Clinvar_Rec_121 RMVar_hsa_circ_93299,RMVar_hsa_circ_212879 40143 RMVar_ID_40143 Human_SNP_ID_698501761 A-to-I Human chr22 + 18088577 18088577 18088577 GAGGTGGGTGGATCACTTGTGGCCAGGAGTTCAAAACCTGCCTGGCCAACATGGTGAAACCCCAT GAGGTGGGTGGATCACTTGTGGCCAGGAGTTCCAAACCTGCCTGGCCAACATGGTGAAACCCCAT A C PEX26 Ensembl:ENSG00000215193 Protein coding 3'UTR GSE38233;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,32596459,32596459 RNA-Seq:(High) rs906368844 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93299,RMVar_hsa_circ_212879 40144 RMVar_ID_40144 Human_SNP_ID_698501774 A-to-I Human chr22 + 18088653 18088653 18088653 ATACAAAAATTAGCTAGATGTGGTGCACGCCTATAGTCCTAGCTACTTGGGAGGCTGAGGCAGGA ATACAAAAATTAGCTAGATGTGGTGCACGCCTGTAGTCCTAGCTACTTGGGAGGCTGAGGCAGGA A G PEX26 Ensembl:ENSG00000215193 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs150745941 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26500533 Human_miRNA_ID_2087349,Human_miRNA_ID_2944608 RMVar_hsa_circ_93299,RMVar_hsa_circ_212879 40145 RMVar_ID_40145 Human_SNP_ID_698501775 A-to-I Human chr22 + 18088655 18088655 18088655 ACAAAAATTAGCTAGATGTGGTGCACGCCTATAGTCCTAGCTACTTGGGAGGCTGAGGCAGGAGA ACAAAAATTAGCTAGATGTGGTGCACGCCTATCGTCCTAGCTACTTGGGAGGCTGAGGCAGGAGA A C PEX26 Ensembl:ENSG00000215193 Protein coding 3'UTR GSE100210;GSE99789;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,EC109;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,29796672,30559470,31158229,31158229,32596459,32596459 RNA-Seq:(High) rs1429107900 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26500533 Human_miRNA_ID_2087349,Human_miRNA_ID_2944608 RMVar_hsa_circ_93299,RMVar_hsa_circ_212879 40146 RMVar_ID_40146 Human_SNP_ID_698501783 A-to-I Human chr22 + 18088710 18088710 18088710 AGGCAGGAGAATCACTTGAGCCAGGGAGGCAAAAGTTGCAGTGAGCTGAGATTGTGCTACCGCAC AGGCAGGAGAATCACTTGAGCCAGGGAGGCAAGAGTTGCAGTGAGCTGAGATTGTGCTACCGCAC A G PEX26 Ensembl:ENSG00000215193 Protein coding 3'UTR GSE123020:GSM3490829,GSM3490830,GSM3490831 esophageal squamous carcinoma cells,EC109 cell line - 32596459 RNA-Seq:(High) rs1456434139 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7060807,Human_RBP_ID_23934618,Human_RBP_ID_26499736 Human_miRNA_ID_2231624 RMVar_hsa_circ_93299,RMVar_hsa_circ_212879 40147 RMVar_ID_40147 Human_SNP_ID_698502137 A-to-I Human chr22 + 18089962 18089962 18089962 CTGAACTTGTGATCCACCCACCTAGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCATCGCG CTGAACTTGTGATCCACCCACCTAGGCCTCCCGAAGTGCTGGGATTACAGGTGTGAGCCATCGCG A G PEX26 Ensembl:ENSG00000215193 Protein coding 3'UTR GSE38233;GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,30559470,31158229,31158229,31158229,32596459,32596459,32596459 RNA-Seq:(High) rs1365794967 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93299,RMVar_hsa_circ_212879 40148 RMVar_ID_40148 Human_SNP_ID_698502138 A-to-I Human chr22 + 18089963 18089963 18089963 TGAACTTGTGATCCACCCACCTAGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCATCGCGC TGAACTTGTGATCCACCCACCTAGGCCTCCCATAGTGCTGGGATTACAGGTGTGAGCCATCGCGC A T PEX26 Ensembl:ENSG00000215193 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,31158229,31158229,32596459,32596459 RNA-Seq:(High) rs1319676195 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93299,RMVar_hsa_circ_212879 40149 RMVar_ID_40149 Human_SNP_ID_698502553 A-to-I Human chr22 + 18091570 18091570 18091570 TGAGGCAGGAGAATCACTTGAACCCGGGAGGCAAGGGTTGCAGTGAGCTGAGATCGCGCCATTGC TGAGGCAGGAGAATCACTTGAACCCGGGAGGCGAGGGTTGCAGTGAGCTGAGATCGCGCCATTGC A G PEX26 Ensembl:ENSG00000215193 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs768456070 Functional Loss SNV dbSNP153 33..33 33 - - - 40150 RMVar_ID_40150 Human_SNP_ID_698502568 A-to-I Human chr22 + 18091628 18091628 18091628 CCATTGCACTCCCACCTGGGCAACAAAGAGTGAAACTTGGTCTCAGAAACGAAACAAAACACAAA CCATTGCACTCCCACCTGGGCAACAAAGAGTGTAACTTGGTCTCAGAAACGAAACAAAACACAAA A T PEX26 Ensembl:ENSG00000215193 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs577489390 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23934639 40151 RMVar_ID_40151 Human_SNP_ID_698502761 A-to-I Human chr22 + 18092362 18092362 18092362 TGCCTCTGGAAACCTCAGTGTTTCGGGCTGGTAGGAAGCTACAGGACAGACAGTGGGCACGGTGC TGCCTCTGGAAACCTCAGTGTTTCGGGCTGGTGGGAAGCTACAGGACAGACAGTGGGCACGGTGC A G PEX26 Ensembl:ENSG00000215193 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs945078155 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1607623,Human_RBP_ID_7060877,Human_RBP_ID_14388372 40152 RMVar_ID_40152 Human_SNP_ID_698503360 A-to-I Human chr22 + 18094351 18094351 18094351 CTCCTGCCTCAGCCTCCCGAGTGGCTGGGACTATAGGCGCCCGCCACCACGCCTGGCTAATTTTT CTCCTGCCTCAGCCTCCCGAGTGGCTGGGACTGTAGGCGCCCGCCACCACGCCTGGCTAATTTTT A G PEX26 Ensembl:ENSG00000215193 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs957688787 Functional Loss SNV dbSNP153 33..33 33 - - - 40153 RMVar_ID_40153 Human_SNP_ID_698503375 A-to-I Human chr22 + 18094397 18094397 18094397 CCACGCCTGGCTAATTTTTTGGTATTTTTAGTAGAGACTGGGTTTCACCGTGTTAGCCAGGATGG CCACGCCTGGCTAATTTTTTGGTATTTTTAGTGGAGACTGGGTTTCACCGTGTTAGCCAGGATGG A G PEX26 Ensembl:ENSG00000215193 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs913625652 Functional Loss SNV dbSNP153 33..33 33 - - - 40154 RMVar_ID_40154 Human_SNP_ID_698504286 A-to-I Human chr22 + 18097788 18097788 18097788 CTGGTGTTGAACTTGCCTCAAGTGATCCTCCCATCTTGACCTCCCAAAGTGCTGGGATTATAGGC CTGGTGTTGAACTTGCCTCAAGTGATCCTCCCGTCTTGACCTCCCAAAGTGCTGGGATTATAGGC A G PEX26 Ensembl:ENSG00000215193 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs373030317 Functional Loss SNV dbSNP153 33..33 33 - - - 40155 RMVar_ID_40155 Human_SNP_ID_698504299 A-to-I Human chr22 + 18097857 18097857 18097857 GCCACCACACCCAGATGATTTTTTTATTTTTCAAAGAAGTGGCATGATTTTGATGACAATAAAGG GCCACCACACCCAGATGATTTTTTTATTTTTCCAAGAAGTGGCATGATTTTGATGACAATAAAGG A C PEX26 Ensembl:ENSG00000215193 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs760546698 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7060967,Human_RBP_ID_14388537 40156 RMVar_ID_40156 Human_SNP_ID_698504329 A-to-I Human chr22 + 18097979 18097979 18097979 CCATGCCCGTAATCCCACCACTTTGGGTGGCCAAGGCAGGTGGATCATGAGGCCAGGAGTTTGAG CCATGCCCGTAATCCCACCACTTTGGGTGGCCGAGGCAGGTGGATCATGAGGCCAGGAGTTTGAG A G PEX26 Ensembl:ENSG00000215193 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs543763346 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17572725 40157 RMVar_ID_40157 Human_SNP_ID_698504345 A-to-I Human chr22 + 18098048 18098048 18098048 GCCTGGCCAACATGATGAAACCCCATCTCTTCAAAAAATCTAAAAATTAGCTGGGTGTGGTGGCG GCCTGGCCAACATGATGAAACCCCATCTCTTCTAAAAATCTAAAAATTAGCTGGGTGTGGTGGCG A T PEX26 Ensembl:ENSG00000215193 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1317138433 Functional Loss SNV dbSNP153 33..33 33 - - - 40158 RMVar_ID_40158 Human_SNP_ID_698505081 A-to-I Human chr22 + 18101453 18101453 18101453 AAAAGACTCATGCTGATTTTGACCTTCCTCTGACCCTTTTCCCTCAACTGCTTGGTGGGGAGTAG AAAAGACTCATGCTGATTTTGACCTTCCTCTGGCCCTTTTCCCTCAACTGCTTGGTGGGGAGTAG A G PEX26 Ensembl:ENSG00000215193 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs361950 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_122,Clinvar_Rec_123 GWAS_ID_4752,GWAS_ID_4753,GWAS_ID_4754,GWAS_ID_4755,GWAS_ID_4756,GWAS_ID_4757 40159 RMVar_ID_40159 Human_SNP_ID_698505082 A-to-I Human chr22 + 18101453 18101453 18101453 AAAAGACTCATGCTGATTTTGACCTTCCTCTGACCCTTTTCCCTCAACTGCTTGGTGGGGAGTAG AAAAGACTCATGCTGATTTTGACCTTCCTCTGTCCCTTTTCCCTCAACTGCTTGGTGGGGAGTAG A T PEX26 Ensembl:ENSG00000215193 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs361950 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_122,Clinvar_Rec_123 GWAS_ID_4752,GWAS_ID_4753,GWAS_ID_4754,GWAS_ID_4755,GWAS_ID_4756,GWAS_ID_4757 40160 RMVar_ID_40160 Human_SNP_ID_698634356 A-to-I Human chr22 - 18924355 18924355 18924355 CAGCCTGGGCAACATGGTGAAACTCCGTCTCCACTAAAATACAAAAAATTAGCCGGGCGTGGCAG CAGCCTGGGCAACATGGTGAAACTCCGTCTCCGCTAAAATACAAAAAATTAGCCGGGCGTGGCAG T C PRODH Ensembl:ENSG00000100033 Protein coding intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs963708934 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85656,RMVar_hsa_circ_212888 40161 RMVar_ID_40161 Human_SNP_ID_698648835 A-to-I Human chr22 + 18981746 18981746 18981746 AGCTCAGGCGATCTTCCTGCCTTGGCTCCCCAAAATACTGGGATTACAGGTGTGAACCACTATGC AGCTCAGGCGATCTTCCTGCCTTGGCTCCCCAGAATACTGGGATTACAGGTGTGAACCACTATGC A G DGCR9,DGCR5 Ensembl:ENSG00000273032,Ensembl:ENSG00000237517 lincRNA,Pseudogene intron,intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1299865976 Functional Loss SNV dbSNP153 33..33 33 - - - 40162 RMVar_ID_40162 Human_SNP_ID_698652849 A-to-I Human chr22 + 18996351 18996351 18996351 CAGCCTGGGCAACATGGCGAAACCCTGTCTCTACCAAAAATACAAAACTTAGCCAGGCATGGTGG CAGCCTGGGCAACATGGCGAAACCCTGTCTCTTCCAAAAATACAAAACTTAGCCAGGCATGGTGG A T DGCR9 Ensembl:ENSG00000273032 lincRNA intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1169728087 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_276915,RMVar_hsa_circ_212890,RMVar_hsa_circ_330611,RMVar_hsa_circ_212893 40163 RMVar_ID_40163 Human_SNP_ID_698656488 A-to-I Human chr22 + 19012422 19012422 19012422 TTTTTTGGGGGGGCAGGTGGGGACAGGGTCTCACTCTGTTGCCTAGGCTGGAGTACAGTGGCGTG TTTTTTGGGGGGGCAGGTGGGGACAGGGTCTCTCTCTGTTGCCTAGGCTGGAGTACAGTGGCGTG A T DGCR9 Ensembl:ENSG00000273032 lincRNA intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs910064201 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_276915,RMVar_hsa_circ_212890,RMVar_hsa_circ_330611,RMVar_hsa_circ_212897,RMVar_hsa_circ_277167,RMVar_hsa_circ_212893,RMVar_hsa_circ_212895,RMVar_hsa_circ_212896,RMVar_hsa_circ_287876,RMVar_hsa_circ_212898 40164 RMVar_ID_40164 Human_SNP_ID_698657619 A-to-I Human chr22 + 19017111 19017111 19017111 CCAGCTACTCCGGAGGCTGAGGCAGGAGAATCACTTGAACCTGGGAGGCAGAGTTTGCTGTGAGC CCAGCTACTCCGGAGGCTGAGGCAGGAGAATCTCTTGAACCTGGGAGGCAGAGTTTGCTGTGAGC A T DGCR9 Ensembl:ENSG00000273032 lincRNA intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs913966777 Functional Loss SNV dbSNP153 33..33 33 - - - 40165 RMVar_ID_40165 Human_SNP_ID_698658639 A-to-I Human chr22 + 19021011 19021011 19021011 TAGCTGGGTTACAGGTGCTAACCACCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGT TAGCTGGGTTACAGGTGCTAACCACCATGCCCGGCTAATTTTTGTATTTTTAGTAGAGACGGGGT A G DGCR9 Ensembl:ENSG00000273032 lincRNA intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs532932749 Functional Loss SNV dbSNP153 33..33 33 - - - 40166 RMVar_ID_40166 Human_SNP_ID_698658790 A-to-I Human chr22 + 19021442 19021442 19021442 TCAAGCCATTCTCCTGCCTCAGCTTCCTGAGCAGCAGGGATTACAGGCATGCGCCACCACACCTG TCAAGCCATTCTCCTGCCTCAGCTTCCTGAGCGGCAGGGATTACAGGCATGCGCCACCACACCTG A G DGCR9 Ensembl:ENSG00000273032 lincRNA intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1005253406 Functional Loss SNV dbSNP153 33..33 33 - - - 40167 RMVar_ID_40167 Human_SNP_ID_698679104 A-to-I Human chr22 - 19089745 19089745 19089745 AAAACCCCGTCTCTACTAAAAATATAAAAATTAGCTAGGCATGATGACACATGCTTGTAATTCCA AAAACCCCGTCTCTACTAAAAATATAAAAATTTGCTAGGCATGATGACACATGCTTGTAATTCCA T A DGCR2 Ensembl:ENSG00000070413 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1168099872 Functional Loss SNV dbSNP153 33..33 33 - - - 40168 RMVar_ID_40168 Human_SNP_ID_698682871 A-to-I Human chr22 - 19103863 19103863 19103863 TTTTATTTTATTTGTAGAGTCAGGGTCTGGCTATGTTGCCCAGGCTGGTCTTGAATTCTTGGACT TTTTATTTTATTTGTAGAGTCAGGGTCTGGCTCTGTTGCCCAGGCTGGTCTTGAATTCTTGGACT T G DGCR2 Ensembl:ENSG00000070413 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1233185946 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14389793 40169 RMVar_ID_40169 Human_SNP_ID_698712642 A-to-I Human chr22 - 19205503 19205501 19205503 AAGGAAATAGTGCTTTTGTTTTGTTTTGAAACAGGGTCTCCTCTGTCACCCAGGCTACAGTGCAG AAGGAAATAGTGCTTTTGTTTTGTTTTGAAAC__GGTCTCCTCTGTCACCCAGGCTACAGTGCAG CCT C CLTCL1 Ensembl:ENSG00000070371 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1260153331 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_2728034 RMVar_hsa_circ_112,RMVar_hsa_circ_30437,RMVar_hsa_circ_42411,RMVar_hsa_circ_8410,RMVar_hsa_circ_17891 40170 RMVar_ID_40170 Human_SNP_ID_698712759 A-to-I Human chr22 - 19206002 19206002 19206002 GACTCACTGGAGGCTGGGAAGTCAAGACTGTAATGAGCTGTGATTGTGCCACTGCACTCCAACCT GACTCACTGGAGGCTGGGAAGTCAAGACTGTATTGAGCTGTGATTGTGCCACTGCACTCCAACCT T A CLTCL1 Ensembl:ENSG00000070371 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886594985 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 40171 RMVar_ID_40171 Human_SNP_ID_698712827 A-to-I Human chr22 - 19206327 19206327 19206327 GAAGTGGGAAGATCACCTGAGCCCAGGAGGTCAAGGCTGCAGTGAGCTGTGATCGGGGTGAGCTG GAAGTGGGAAGATCACCTGAGCCCAGGAGGTCGAGGCTGCAGTGAGCTGTGATCGGGGTGAGCTG T C CLTCL1 Ensembl:ENSG00000070371 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs929739750 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 40172 RMVar_ID_40172 Human_SNP_ID_698719093 A-to-I Human chr22 - 19230475 19230475 19230475 TCAAGGAATGCATCCACCTCAGCCTCCTGAGTAGCTGGGACTATAGGCACATGCCACCACACCTG TCAAGGAATGCATCCACCTCAGCCTCCTGAGTGGCTGGGACTATAGGCACATGCCACCACACCTG T C CLTCL1 Ensembl:ENSG00000070371 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs375774798 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34063,RMVar_hsa_circ_17891,RMVar_hsa_circ_293649,RMVar_hsa_circ_38776,RMVar_hsa_circ_106012,RMVar_hsa_circ_212921,RMVar_hsa_circ_112806,RMVar_hsa_circ_369961,RMVar_hsa_circ_212922,RMVar_hsa_circ_303597,RMVar_hsa_circ_212923 40173 RMVar_ID_40173 Human_SNP_ID_698719094 A-to-I Human chr22 - 19230475 19230475 19230475 TCAAGGAATGCATCCACCTCAGCCTCCTGAGTAGCTGGGACTATAGGCACATGCCACCACACCTG TCAAGGAATGCATCCACCTCAGCCTCCTGAGTCGCTGGGACTATAGGCACATGCCACCACACCTG T G CLTCL1 Ensembl:ENSG00000070371 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs375774798 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34063,RMVar_hsa_circ_17891,RMVar_hsa_circ_293649,RMVar_hsa_circ_38776,RMVar_hsa_circ_106012,RMVar_hsa_circ_212921,RMVar_hsa_circ_112806,RMVar_hsa_circ_369961,RMVar_hsa_circ_212922,RMVar_hsa_circ_303597,RMVar_hsa_circ_212923 40174 RMVar_ID_40174 Human_SNP_ID_698729177 A-to-I Human chr22 - 19271993 19271993 19271993 ACGATCCTCCTGCGTCAGCCTCTGAAGTAGCTAGGACTACAGGCACATGCCACCATGCCCAGCTA ACGATCCTCCTGCGTCAGCCTCTGAAGTAGCTGGGACTACAGGCACATGCCACCATGCCCAGCTA T C CLTCL1 Ensembl:ENSG00000070371 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs899053734 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38776,RMVar_hsa_circ_351045,RMVar_hsa_circ_329054 40175 RMVar_ID_40175 Human_SNP_ID_698735057 A-to-I Human chr22 + 19294961 19294961 19294961 GGAGGATCACTTGAGCCCATGAGCTCAAGGTTACAGTAAGCTATGATCGTACCACTATACTCCAG GGAGGATCACTTGAGCCCATGAGCTCAAGGTTGCAGTAAGCTATGATCGTACCACTATACTCCAG A G AC000085.1 Ensembl:ENSG00000287146 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1555997150 Functional Loss SNV dbSNP153 33..33 33 - - - 40176 RMVar_ID_40176 Human_SNP_ID_698744324 A-to-I Human chr22 - 19334668 19334668 19334668 GCCTTAATCCCAGCACTTTGGGAGGCCAAGGCAGGTGGATCACCTGAGGTCAGGACTGGCTAATT GCCTTAATCCCAGCACTTTGGGAGGCCAAGGCCGGTGGATCACCTGAGGTCAGGACTGGCTAATT T G HIRA Ensembl:ENSG00000100084 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1465085742 Functional Loss SNV dbSNP153 33..33 33 - - - 40177 RMVar_ID_40177 Human_SNP_ID_698754752 A-to-I Human chr22 - 19379303 19379299 19379304 GTATTTCTACTTTGAAAAACTGCCGGCCGGGCACGGTGGCTCACACCTGTAATCCCAGCACTTTG GTATTTCTACTTTGAAAAACTGCCGGCCGGG_____TGGCTCACACCTGTAATCCCAGCACTTTG ACCGTG A HIRA,C22orf39 Ensembl:ENSG00000100084,Ensembl:ENSG00000242259 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1166298910 Functional Loss DEL dbSNP153 32..36 33 - - - RMVar_hsa_circ_9326,RMVar_hsa_circ_32381,RMVar_hsa_circ_275365,RMVar_hsa_circ_5180,RMVar_hsa_circ_11373,RMVar_hsa_circ_266928,RMVar_hsa_circ_297832,RMVar_hsa_circ_75794,RMVar_hsa_circ_212930,RMVar_hsa_circ_370065,RMVar_hsa_circ_68495,RMVar_hsa_circ_16983,RMVar_hsa_circ_212932,RMVar_hsa_circ_212933 40178 RMVar_ID_40178 Human_SNP_ID_698763597 A-to-I Human chr22 - 19416614 19416614 19416614 AAATTCATGGTCAGATGCAGTGGTGCACGCCTATAATCCTAGCACTTTGGGACGTAAAGGTAGCA AAATTCATGGTCAGATGCAGTGGTGCACGCCTGTAATCCTAGCACTTTGGGACGTAAAGGTAGCA T C HIRA,C22orf39 Ensembl:ENSG00000100084,Ensembl:ENSG00000242259 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1419286827 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_212937,RMVar_hsa_circ_115706 40179 RMVar_ID_40179 Human_SNP_ID_698768898 A-to-I Human chr22 - 19436377 19436377 19436377 TTAATTCTGGCTGGGCGTGGTGGCTGATGCCTATAATCCCAGTGCTTTGGGAGGCCAAGGTAGGC TTAATTCTGGCTGGGCGTGGTGGCTGATGCCTGTAATCCCAGTGCTTTGGGAGGCCAAGGTAGGC T C HIRA,C22orf39 Ensembl:ENSG00000100084,Ensembl:ENSG00000242259 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs939073535 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_212937,RMVar_hsa_circ_115706 40180 RMVar_ID_40180 Human_SNP_ID_698770249 A-to-I Human chr22 - 19441657 19441657 19441657 AAGTGTGGTGGCTCACACCTGTAATCTCAGCTACTTGGGAGGCTGAGGCAGAAGAATCACTTGAG AAGTGTGGTGGCTCACACCTGTAATCTCAGCTGCTTGGGAGGCTGAGGCAGAAGAATCACTTGAG T C HIRA,C22orf39 Ensembl:ENSG00000100084,Ensembl:ENSG00000242259 Protein coding,Protein coding intron,intron GSE56152 embryonic stem cells,wild type - 25708366 RNA-Seq:(High) rs1395614506 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_575288,Human_RBP_ID_22819417,Human_RBP_ID_23010705,Human_RBP_ID_27031521 Human_Splice_Rec_2137042,Human_Splice_Rec_2137046 RMVar_hsa_circ_212937,RMVar_hsa_circ_115706,RMVar_hsa_circ_212952,RMVar_hsa_circ_109523 40181 RMVar_ID_40181 Human_SNP_ID_698772641 A-to-I Human chr22 - 19450739 19450739 19450739 AAAATAGTATCTTCTCTTCAAACCTAGGATGAAGCTGGAGGCAGATTCGTCGCTTTCTCTGGAGA AAAATAGTATCTTCTCTTCAAACCTAGGATGATGCTGGAGGCAGATTCGTCGCTTTCTCTGGAGA T A UFD1 Ensembl:ENSG00000070010 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs756284366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_780927,Human_RBP_ID_932449,Human_RBP_ID_14393755,Human_RBP_ID_22673893,Human_RBP_ID_23935247,Human_RBP_ID_24561083,Human_RBP_ID_25680553 Human_Splice_Rec_2137098,Human_Splice_Rec_2137140,Human_Splice_Rec_2137154 RMVar_hsa_circ_104711,RMVar_hsa_circ_212954 40182 RMVar_ID_40182 Human_SNP_ID_698772732 A-to-I Human chr22 - 19451119 19451118 19451119 CTTACAGACTTTTTTTTTTTTTTTTTTTTTTGAGGCAGGGTCTTGCTCTGTTGCTCTGCCATCCA CTTACAGACTTTTTTTTTTTTTTTTTTTTTTG_GGCAGGGTCTTGCTCTGTTGCTCTGCCATCCA CT C UFD1 Ensembl:ENSG00000070010 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1292305452 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_780928,Human_RBP_ID_932450,Human_RBP_ID_14393775 RMVar_hsa_circ_104711,RMVar_hsa_circ_212954 40183 RMVar_ID_40183 Human_SNP_ID_698772734 A-to-I Human chr22 - 19451119 19451119 19451119 CTTACAGACTTTTTTTTTTTTTTTTTTTTTTGAGGCAGGGTCTTGCTCTGTTGCTCTGCCATCCA CTTACAGACTTTTTTTTTTTTTTTTTTTTTTGTGGCAGGGTCTTGCTCTGTTGCTCTGCCATCCA T A UFD1 Ensembl:ENSG00000070010 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1243964453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_780928,Human_RBP_ID_932450,Human_RBP_ID_14393775 RMVar_hsa_circ_104711,RMVar_hsa_circ_212954 40184 RMVar_ID_40184 Human_SNP_ID_698773115 A-to-I Human chr22 - 19452813 19452813 19452813 CCATGCATTAAGGACATCATCAGCCAAGCGCCATGGCTCACACCTGTAATCCCAACACTTTGGGA CCATGCATTAAGGACATCATCAGCCAAGCGCCGTGGCTCACACCTGTAATCCCAACACTTTGGGA T C UFD1 Ensembl:ENSG00000070010 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs940919994 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14393862 RMVar_hsa_circ_104711,RMVar_hsa_circ_212954 40185 RMVar_ID_40185 Human_SNP_ID_698774616 A-to-I Human chr22 - 19459493 19459493 19459493 CTCCTGCCTCAGCCTCCCGAATAGCTGGGACTACAGGCACCTGCCACCACTCCCAGCTAATTTTT CTCCTGCCTCAGCCTCCCGAATAGCTGGGACTGCAGGCACCTGCCACCACTCCCAGCTAATTTTT T C UFD1 Ensembl:ENSG00000070010 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs540157322 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7550,RMVar_hsa_circ_104711,RMVar_hsa_circ_212954,RMVar_hsa_circ_64752 40186 RMVar_ID_40186 Human_SNP_ID_698774739 A-to-I Human chr22 - 19459883 19459883 19459883 AACACAAAAATTAGCTGGGTGTGGTGGCACGCACCTGTAGTCCCAGTTACTTGGGAGGCTGAGGC AACACAAAAATTAGCTGGGTGTGGTGGCACGCGCCTGTAGTCCCAGTTACTTGGGAGGCTGAGGC T C UFD1 Ensembl:ENSG00000070010 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1233396253 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7550,RMVar_hsa_circ_104711,RMVar_hsa_circ_212954,RMVar_hsa_circ_64752 40187 RMVar_ID_40187 Human_SNP_ID_698784913 A-to-I Human chr22 + 19500530 19500530 19500530 CTGCTCCATAGATCACAACTTGAACCTTAGGAAATGCCGTTTTCCCTTTGAGATATTTCTTTGGG CTGCTCCATAGATCACAACTTGAACCTTAGGATATGCCGTTTTCCCTTTGAGATATTTCTTTGGG A T CDC45 Ensembl:ENSG00000093009 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs976077370 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_685,RMVar_hsa_circ_15497,RMVar_hsa_circ_375700,RMVar_hsa_circ_212964 40188 RMVar_ID_40188 Human_SNP_ID_698841193 A-to-I Human chr22 + 19717132 19717132 19717132 AGGCCCCACAACAGGACCAGGGCCTGGACAGGAAGTGGAGGAGGTCTCTCAGCCAGGAGAGCCTA AGGCCCCACAACAGGACCAGGGCCTGGACAGGGAGTGGAGGAGGTCTCTCAGCCAGGAGAGCCTA A G SEPTIN5 Ensembl:ENSG00000184702 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs146627613 Functional Loss SNV dbSNP153 33..33 33 - - - 40189 RMVar_ID_40189 Human_SNP_ID_698873330 A-to-I Human chr22 - 19828398 19828398 19828398 CTTCCACCTCAGCCTCCCAAAGTGTTGGGACTACAGGTGTGAGCCCACCACACCTGGCAATAAAC CTTCCACCTCAGCCTCCCAAAGTGTTGGGACTGCAGGTGTGAGCCCACCACACCTGGCAATAAAC T C GNB1L Ensembl:ENSG00000185838 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs969356575 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55021 40190 RMVar_ID_40190 Human_SNP_ID_698895048 A-to-I Human chr22 - 19910699 19910699 19910699 GGAGGCTTTAGGTGGGAGGATTGCTTGAGCCCAGGAGGTTGAGGCTGCAGTGAGCTGTGATTGCA GGAGGCTTTAGGTGGGAGGATTGCTTGAGCCCGGGAGGTTGAGGCTGCAGTGAGCTGTGATTGCA T C TXNRD2 Ensembl:ENSG00000184470 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs963783155 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17572935 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 40191 RMVar_ID_40191 Human_SNP_ID_698900894 A-to-I Human chr22 - 19931642 19931642 19931642 AAATTTAGCTGGACGTGGTGATCGGTGCTTGTAGTCCCAGCTATTCTGGAGGCTGAGGCTAGAGG AAATTTAGCTGGACGTGGTGATCGGTGCTTGTGGTCCCAGCTATTCTGGAGGCTGAGGCTAGAGG T C TXNRD2 Ensembl:ENSG00000184470 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1408779114 Functional Loss SNV dbSNP153 33..33 33 - - - 40192 RMVar_ID_40192 Human_SNP_ID_698900914 A-to-I Human chr22 - 19931706 19931706 19931706 TTGAGGCCAGGTGTTTGAGACCAGCCTGGGCAACATAGCCAGACCCCATCTCTACAAAACAAAAA TTGAGGCCAGGTGTTTGAGACCAGCCTGGGCAGCATAGCCAGACCCCATCTCTACAAAACAAAAA T C TXNRD2 Ensembl:ENSG00000184470 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1385610504 Functional Loss SNV dbSNP153 33..33 33 - - - 40193 RMVar_ID_40193 Human_SNP_ID_698904303 A-to-I Human chr22 + 19943519 19943519 19943519 TAAAAATTAGCCCGGCGTGGTGGCATGGGCCTATAGTTCCAGCTACTTGGGAGGCTGAGGTGAAA TAAAAATTAGCCCGGCGTGGTGGCATGGGCCTGTAGTTCCAGCTACTTGGGAGGCTGAGGTGAAA A G COMT Ensembl:ENSG00000093010 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs550109761 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25655232 40194 RMVar_ID_40194 Human_SNP_ID_698904304 A-to-I Human chr22 + 19943521 19943521 19943521 AAAATTAGCCCGGCGTGGTGGCATGGGCCTATAGTTCCAGCTACTTGGGAGGCTGAGGTGAAAAG AAAATTAGCCCGGCGTGGTGGCATGGGCCTATTGTTCCAGCTACTTGGGAGGCTGAGGTGAAAAG A T COMT Ensembl:ENSG00000093010 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1052573650 Functional Loss SNV dbSNP153 33..33 33 - - - 40195 RMVar_ID_40195 Human_SNP_ID_698905534 A-to-I Human chr22 + 19948440 19948440 19948440 ACTTTGGGAGTCCGAGGAGGGAGGACTCCTTGAGCCCAGGAGTTTGAGACCAGCCTGAGAAACAT ACTTTGGGAGTCCGAGGAGGGAGGACTCCTTGTGCCCAGGAGTTTGAGACCAGCCTGAGAAACAT A T COMT Ensembl:ENSG00000093010 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1205611698 Functional Loss SNV dbSNP153 33..33 33 - - - 40196 RMVar_ID_40196 Human_SNP_ID_698905586 A-to-I Human chr22 + 19948697 19948697 19948697 AAAATTTAGGCTGGGTGCAGCGGCTCACGCCTATAATCCCAGCATTTTGGGAGGTCAAGGTGGAC AAAATTTAGGCTGGGTGCAGCGGCTCACGCCTGTAATCCCAGCATTTTGGGAGGTCAAGGTGGAC A G COMT Ensembl:ENSG00000093010 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs983453457 Functional Loss SNV dbSNP153 33..33 33 - - - 40197 RMVar_ID_40197 Human_SNP_ID_698905713 A-to-I Human chr22 + 19949236 19949236 19949236 TCAGCTTACTGCAGCCTTGACCTCCTGGGCTCAAGCGATCCTCCTGCCTCACCCTCCCAAGTAGC TCAGCTTACTGCAGCCTTGACCTCCTGGGCTCCAGCGATCCTCCTGCCTCACCCTCCCAAGTAGC A C COMT Ensembl:ENSG00000093010 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1418255362 Functional Loss SNV dbSNP153 33..33 33 - - - 40198 RMVar_ID_40198 Human_SNP_ID_698905801 A-to-I Human chr22 + 19949697 19949697 19949697 AGGACTCACTGCACCCTTGAACTCCCGGGCTCAAGTAATTCTCCAACCTCAGCCCCCTAAAGCAC AGGACTCACTGCACCCTTGAACTCCCGGGCTCCAGTAATTCTCCAACCTCAGCCCCCTAAAGCAC A C COMT Ensembl:ENSG00000093010 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1441624300 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14397902 40199 RMVar_ID_40199 Human_SNP_ID_698905983 A-to-I Human chr22 + 19950294 19950294 19950294 TTCTGTAGAGACAAGGTCTTGCTGTGTTGCCCAGGCTGGTCTTGAACTCCTAGCCTCAAGTGATC TTCTGTAGAGACAAGGTCTTGCTGTGTTGCCCCGGCTGGTCTTGAACTCCTAGCCTCAAGTGATC A C COMT Ensembl:ENSG00000093010 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1410567387 Functional Loss SNV dbSNP153 33..33 33 - - - 40200 RMVar_ID_40200 Human_SNP_ID_100538419 A-to-I Human chr2 - 165862076 165862074 165862077 CCTGAGACTGGACAATTTACAGAAAAAAAAGAAGTTTAGTGGGACTTACAGTTCTACTTGCCTGG CCTGAGACTGGACAATTTACAGAAAAAAAAG___TTTAGTGGGACTTACAGTTCTACTTGCCTGG ACTT A TTC21B Ensembl:ENSG00000123607 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355493168 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_85403,RMVar_hsa_circ_65106,RMVar_hsa_circ_204301 40201 RMVar_ID_40201 Human_SNP_ID_100540276 A-to-I Human chr2 - 165869858 165869858 165869858 CCGAGATCACGCCACTGCACTCCAGCCTGGGCAACAGTGAGATTCCGTCTAAAAAAAAAAAAAAA CCGAGATCACGCCACTGCACTCCAGCCTGGGCGACAGTGAGATTCCGTCTAAAAAAAAAAAAAAA T C TTC21B Ensembl:ENSG00000123607 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934765945 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85403,RMVar_hsa_circ_65106,RMVar_hsa_circ_204301 40202 RMVar_ID_40202 Human_SNP_ID_100541378 A-to-I Human chr2 - 165874182 165874182 165874182 GCCATCACACCCGGCTAATTTTTTGTATTTTTAGTAGAGATGGGATTTCACCGTGTTAGCCAGGA GCCATCACACCCGGCTAATTTTTTGTATTTTTCGTAGAGATGGGATTTCACCGTGTTAGCCAGGA T G TTC21B Ensembl:ENSG00000123607 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs937537378 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117441,RMVar_hsa_circ_85403,RMVar_hsa_circ_81716,RMVar_hsa_circ_204301,RMVar_hsa_circ_204303,RMVar_hsa_circ_204304,RMVar_hsa_circ_204302,RMVar_hsa_circ_204305 40203 RMVar_ID_40203 Human_SNP_ID_100541396 A-to-I Human chr2 - 165874234 165874234 165874234 TTACGCGATTCTCCTGCTTCAGCCTCCCGAGTAGCTGGGACTAAAGGCATGTGCCATCACACCCG TTACGCGATTCTCCTGCTTCAGCCTCCCGAGTGGCTGGGACTAAAGGCATGTGCCATCACACCCG T C TTC21B Ensembl:ENSG00000123607 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1455081053 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117441,RMVar_hsa_circ_85403,RMVar_hsa_circ_81716,RMVar_hsa_circ_204301,RMVar_hsa_circ_204303,RMVar_hsa_circ_204304,RMVar_hsa_circ_204302,RMVar_hsa_circ_204305 40204 RMVar_ID_40204 Human_SNP_ID_100541506 A-to-I Human chr2 - 165874716 165874716 165874716 TTTTAACTTAGGTGTTGGTTTAACAGGAAATGAAAGAAATCTAACTTTCAGTTCTTCCTGTTCAA TTTTAACTTAGGTGTTGGTTTAACAGGAAATGGAAGAAATCTAACTTTCAGTTCTTCCTGTTCAA T C TTC21B Ensembl:ENSG00000123607 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs768656308 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_317015 RMVar_hsa_circ_117441,RMVar_hsa_circ_85403,RMVar_hsa_circ_81716,RMVar_hsa_circ_204301,RMVar_hsa_circ_204303,RMVar_hsa_circ_204304,RMVar_hsa_circ_204302,RMVar_hsa_circ_204305 40205 RMVar_ID_40205 Human_SNP_ID_100543794 A-to-I Human chr2 - 165883919 165883919 165883919 CCAGAAACCAGCTGAAGCGTATTGCGAAAATGAATTGGAATGCTATTGATGCTGAAGAGTTTGAG CCAGAAACCAGCTGAAGCGTATTGCGAAAATGGATTGGAATGCTATTGATGCTGAAGAGTTTGAG T C TTC21B Ensembl:ENSG00000123607 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs758150944 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9384968,Human_RBP_ID_18748748,Human_RBP_ID_23834681,Human_RBP_ID_26338722,Human_RBP_ID_27817710 Human_Splice_Rec_317008,Human_Splice_Rec_317072,Human_Splice_Rec_317128 Human_miRNA_ID_1786071,Human_miRNA_ID_1952797 RMVar_hsa_circ_1098,RMVar_hsa_circ_117441,RMVar_hsa_circ_204303,RMVar_hsa_circ_204304,RMVar_hsa_circ_307818,RMVar_hsa_circ_39447,RMVar_hsa_circ_204305,RMVar_hsa_circ_358216,RMVar_hsa_circ_370833,RMVar_hsa_circ_319991,RMVar_hsa_circ_23280,RMVar_hsa_circ_298933,RMVar_hsa_circ_21387,RMVar_hsa_circ_41411,RMVar_hsa_circ_79892,RMVar_hsa_circ_204306,RMVar_hsa_circ_204307,RMVar_hsa_circ_59854,RMVar_hsa_circ_204308 40206 RMVar_ID_40206 Human_SNP_ID_100551937 A-to-I Human chr2 - 165916080 165916080 165916080 GAGGGTCTCCCTATGTTATGCAGGATGGTCTCAAACTACTGGGCTTAAGTGATCCACCCAGCTCG GAGGGTCTCCCTATGTTATGCAGGATGGTCTCCAACTACTGGGCTTAAGTGATCCACCCAGCTCG T G TTC21B Ensembl:ENSG00000123607 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs966116254 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117441,RMVar_hsa_circ_39447,RMVar_hsa_circ_204305,RMVar_hsa_circ_358216,RMVar_hsa_circ_21387,RMVar_hsa_circ_15149,RMVar_hsa_circ_41411,RMVar_hsa_circ_59854,RMVar_hsa_circ_53833,RMVar_hsa_circ_120208,RMVar_hsa_circ_339570,RMVar_hsa_circ_311016,RMVar_hsa_circ_119188,RMVar_hsa_circ_204315,RMVar_hsa_circ_204316,RMVar_hsa_circ_204314,RMVar_hsa_circ_25325,RMVar_hsa_circ_340905,RMVar_hsa_circ_18038,RMVar_hsa_circ_19766,RMVar_hsa_circ_315219,RMVar_hsa_circ_335676,RMVar_hsa_circ_31192,RMVar_hsa_circ_68834,RMVar_hsa_circ_204318,RMVar_hsa_circ_96825,RMVar_hsa_circ_346356,RMVar_hsa_circ_204319,RMVar_hsa_circ_204320,RMVar_hsa_circ_62874,RMVar_hsa_circ_9064,RMVar_hsa_circ_340140,RMVar_hsa_circ_26357 40207 RMVar_ID_40207 Human_SNP_ID_100578937 A-to-I Human chr2 - 166023852 166023852 166023852 GGAATCGCTTGAGCCCGGGAGGCAGAGGTCACAGTGAGCCGAGATTGCGCCATTGCACTCCAGCC GGAATCGCTTGAGCCCGGGAGGCAGAGGTCACGGTGAGCCGAGATTGCGCCATTGCACTCCAGCC T C SCN1A Ensembl:ENSG00000144285 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1376831245 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40761,RMVar_hsa_circ_330772,RMVar_hsa_circ_264936,RMVar_hsa_circ_204327 40208 RMVar_ID_40208 Human_SNP_ID_101071365 A-to-I Human chr2 - 167962817 167962817 167962817 GGAAGCTGCAGACTCCCCCCTGGTCTAGCCTCAGTGCCCACGCTCTCAACAGCCATTCATCTTGG GGAAGCTGCAGACTCCCCCCTGGTCTAGCCTCGGTGCCCACGCTCTCAACAGCCATTCATCTTGG T C STK39 Ensembl:ENSG00000198648 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006330981 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_204359,RMVar_hsa_circ_123659,RMVar_hsa_circ_106976,RMVar_hsa_circ_204358 40209 RMVar_ID_40209 Human_SNP_ID_101292278 A-to-I Human chr2 - 168888182 168888182 168888182 GCCTCGACCTCCTCGGCTCAAGTGATACTCCCACTTCACCCCCTAAGTAGCTGGGACCACTGGTG GCCTCGACCTCCTCGGCTCAAGTGATACTCCCGCTTCACCCCCTAAGTAGCTGGGACCACTGGTG T C SPC25 Ensembl:ENSG00000152253 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1178867910 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_204415 40210 RMVar_ID_40210 Human_SNP_ID_101458751 A-to-I Human chr2 - 169537626 169537626 169537626 ATCCCAGCACTTTGGGAGGCTGAAAGGCGGGCAGATCACCTGAGGTCAGGAGTTCGAGACCAGCC ATCCCAGCACTTTGGGAGGCTGAAAGGCGGGCGGATCACCTGAGGTCAGGAGTTCGAGACCAGCC T C FASTKD1 Ensembl:ENSG00000138399 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1175207157 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_143678 RMVar_hsa_circ_204432,RMVar_hsa_circ_1959,RMVar_hsa_circ_204423,RMVar_hsa_circ_92980,RMVar_hsa_circ_115503,RMVar_hsa_circ_204424,RMVar_hsa_circ_275076,RMVar_hsa_circ_339656,RMVar_hsa_circ_204425,RMVar_hsa_circ_366897,RMVar_hsa_circ_312371,RMVar_hsa_circ_63096,RMVar_hsa_circ_112090,RMVar_hsa_circ_204427,RMVar_hsa_circ_204428,RMVar_hsa_circ_204429,RMVar_hsa_circ_204426,RMVar_hsa_circ_288408,RMVar_hsa_circ_204430,RMVar_hsa_circ_45365,RMVar_hsa_circ_342305,RMVar_hsa_circ_360970,RMVar_hsa_circ_368858,RMVar_hsa_circ_309554,RMVar_hsa_circ_204434,RMVar_hsa_circ_278907,RMVar_hsa_circ_204433,RMVar_hsa_circ_108248,RMVar_hsa_circ_204431,RMVar_hsa_circ_362034,RMVar_hsa_circ_204435 40211 RMVar_ID_40211 Human_SNP_ID_101467812 A-to-I Human chr2 - 169570955 169570955 169570955 AAGATTAATGCCAGTCGGGTGTGGTGACTCACACTTGTAATCCCAGCACTTTGGGAGGCTGAGGT AAGATTAATGCCAGTCGGGTGTGGTGACTCACCCTTGTAATCCCAGCACTTTGGGAGGCTGAGGT T G FASTKD1 Ensembl:ENSG00000138399 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1306463232 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_339656,RMVar_hsa_circ_204426,RMVar_hsa_circ_368858,RMVar_hsa_circ_204439,RMVar_hsa_circ_362406,RMVar_hsa_circ_103746,RMVar_hsa_circ_34119 40212 RMVar_ID_40212 Human_SNP_ID_101467945 A-to-I Human chr2 - 169571450 169571450 169571450 ACGCCATTCTCCTGCCTCAGCCTTCCGAGTCAATGGGACTACAGGCGCCTGCCACCACGCCCGGC ACGCCATTCTCCTGCCTCAGCCTTCCGAGTCAGTGGGACTACAGGCGCCTGCCACCACGCCCGGC T C FASTKD1 Ensembl:ENSG00000138399 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1447032973 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_339656,RMVar_hsa_circ_204426,RMVar_hsa_circ_368858,RMVar_hsa_circ_204439,RMVar_hsa_circ_362406,RMVar_hsa_circ_103746,RMVar_hsa_circ_34119 40213 RMVar_ID_40213 Human_SNP_ID_101480698 A-to-I Human chr2 + 169615307 169615307 169615307 CTGACTTTGTGATCCGCCTGCCTTGGCCCCCCAAAGTGCTGGGATTACAGGTGTGAGCCACTGCA CTGACTTTGTGATCCGCCTGCCTTGGCCCCCCGAAGTGCTGGGATTACAGGTGTGAGCCACTGCA A G PPIG Ensembl:ENSG00000138398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1201540119 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26760533 RMVar_hsa_circ_14292,RMVar_hsa_circ_267844,RMVar_hsa_circ_28091 40214 RMVar_ID_40214 Human_SNP_ID_101502146 A-to-I Human chr2 + 169702492 169702492 169702492 GATTCAAGTGATCCTCCTGCCTTGGTTTCCCAAAGTTCTGGGATTACAGGCATGAGCCACTGTGG GATTCAAGTGATCCTCCTGCCTTGGTTTCCCAGAGTTCTGGGATTACAGGCATGAGCCACTGTGG A G KLHL23 Ensembl:ENSG00000213160 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1482325513 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17570027 RMVar_hsa_circ_204463,RMVar_hsa_circ_78738 40215 RMVar_ID_40215 Human_SNP_ID_101502304 A-to-I Human chr2 + 169703227 169703227 169703227 CCAATATTCAGTTCGTAGCAAACTACTGGAACAAGAATCTGTTTTCTTGCTGAGTGAATTTCTTG CCAATATTCAGTTCGTAGCAAACTACTGGAACGAGAATCTGTTTTCTTGCTGAGTGAATTTCTTG A G KLHL23 Ensembl:ENSG00000213160 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1193617117 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17697608 RMVar_hsa_circ_204463,RMVar_hsa_circ_78738 40216 RMVar_ID_40216 Human_SNP_ID_101502325 A-to-I Human chr2 + 169703333 169703333 169703333 TGAGCACAATGGCGCACACCTGTAATCCCAGCAGTTTGGGAAGCCAAAGTAGGAGGATCGCTTGA TGAGCACAATGGCGCACACCTGTAATCCCAGCGGTTTGGGAAGCCAAAGTAGGAGGATCGCTTGA A G KLHL23 Ensembl:ENSG00000213160 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167976877 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_204463,RMVar_hsa_circ_78738 40217 RMVar_ID_40217 Human_SNP_ID_101502327 A-to-I Human chr2 + 169703347 169703347 169703347 CACACCTGTAATCCCAGCAGTTTGGGAAGCCAAAGTAGGAGGATCGCTTGAGGCCAGGAGTTCAA CACACCTGTAATCCCAGCAGTTTGGGAAGCCAGAGTAGGAGGATCGCTTGAGGCCAGGAGTTCAA A G KLHL23 Ensembl:ENSG00000213160 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs764900821 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_204463,RMVar_hsa_circ_78738 40218 RMVar_ID_40218 Human_SNP_ID_101502377 A-to-I Human chr2 + 169703588 169703588 169703588 CCTTTAATCCCAGCACTTTGGGAGGCAAGGCTAGGGGATCACTTGAGCTCAGGAGTTTGAGAACA CCTTTAATCCCAGCACTTTGGGAGGCAAGGCTGGGGGATCACTTGAGCTCAGGAGTTTGAGAACA A G KLHL23 Ensembl:ENSG00000213160 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1137551 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243276,Human_RBP_ID_776731,Human_RBP_ID_6847285,Human_RBP_ID_13670171 RMVar_hsa_circ_204463,RMVar_hsa_circ_78738 40219 RMVar_ID_40219 Human_SNP_ID_101503736 A-to-I Human chr2 + 169709473 169709473 169709473 GACTTGTTTTTTTTTTTTTTTTTTTTGGAGACAGTGTCTCTGTAGCCCAGGCTGGAGTGCAGTGA GACTTGTTTTTTTTTTTTTTTTTTTTGGAGACGGTGTCTCTGTAGCCCAGGCTGGAGTGCAGTGA A G KLHL23 Ensembl:ENSG00000213160 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335290514 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14001256,Human_RBP_ID_25479650 RMVar_hsa_circ_204463,RMVar_hsa_circ_78738 40220 RMVar_ID_40220 Human_SNP_ID_101503746 A-to-I Human chr2 + 169709545 169709545 169709545 ACAGCTCACTGCAACCTCAAACTCCTGGACTTAAGCAATCTTCCAGTCTCAGCCTCCCAAGTAGC ACAGCTCACTGCAACCTCAAACTCCTGGACTTGAGCAATCTTCCAGTCTCAGCCTCCCAAGTAGC A G KLHL23 Ensembl:ENSG00000213160 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1192241083 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_204463,RMVar_hsa_circ_78738 40221 RMVar_ID_40221 Human_SNP_ID_101503748 A-to-I Human chr2 + 169709549 169709549 169709549 CTCACTGCAACCTCAAACTCCTGGACTTAAGCAATCTTCCAGTCTCAGCCTCCCAAGTAGCTGGG CTCACTGCAACCTCAAACTCCTGGACTTAAGCGATCTTCCAGTCTCAGCCTCCCAAGTAGCTGGG A G KLHL23 Ensembl:ENSG00000213160 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs572905333 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_204463,RMVar_hsa_circ_78738 40222 RMVar_ID_40222 Human_SNP_ID_101514434 A-to-I Human chr2 + 169750017 169750014 169750018 ACGTATGTATACATATATGTGTATATATACGTATGTATGTATACATATGTGTATATATAGTATGT ACGTATGTATACATATATGTGTATATATAC____GTATGTATACATATGTGTATATATAGTATGT CGTAT C KLHL23 Ensembl:ENSG00000213160 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1165350840 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_17570031,Human_RBP_ID_27688591 40223 RMVar_ID_40223 Human_SNP_ID_101514437 A-to-I Human chr2 + 169750017 169750015 169750017 ACGTATGTATACATATATGTGTATATATACGTATGTATGTATACATATGTGTATATATAGTATGT ACGTATGTATACATATATGTGTATATATACG__TGTATGTATACATATGTGTATATATAGTATGT GTA G KLHL23 Ensembl:ENSG00000213160 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1160381083 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_17570031,Human_RBP_ID_27688591 40224 RMVar_ID_40224 Human_SNP_ID_101514439 A-to-I Human chr2 + 169750017 169750017 169750017 ACGTATGTATACATATATGTGTATATATACGTATGTATGTATACATATGTGTATATATAGTATGT ACGTATGTATACATATATGTGTATATATACGTGTGTATGTATACATATGTGTATATATAGTATGT A G KLHL23 Ensembl:ENSG00000213160 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs10209295 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17570031,Human_RBP_ID_27688591 40225 RMVar_ID_40225 Human_SNP_ID_101514440 A-to-I Human chr2 + 169750017 169750017 169750017 ACGTATGTATACATATATGTGTATATATACGTATGTATGTATACATATGTGTATATATAGTATGT ACGTATGTATACATATATGTGTATATATACGTTTGTATGTATACATATGTGTATATATAGTATGT A T KLHL23 Ensembl:ENSG00000213160 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs10209295 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17570031,Human_RBP_ID_27688591 40226 RMVar_ID_40226 Human_SNP_ID_101514680 A-to-I Human chr2 + 169750214 169750214 169750214 TACCTATAATCTCTGGTTTTCAAAGGTAATATAGAATATTTGACACTTGGTAAAAGGTGAACTAC TACCTATAATCTCTGGTTTTCAAAGGTAATATGGAATATTTGACACTTGGTAAAAGGTGAACTAC A G KLHL23 Ensembl:ENSG00000213160 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10164599 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26477881 40227 RMVar_ID_40227 Human_SNP_ID_101514681 A-to-I Human chr2 + 169750214 169750214 169750214 TACCTATAATCTCTGGTTTTCAAAGGTAATATAGAATATTTGACACTTGGTAAAAGGTGAACTAC TACCTATAATCTCTGGTTTTCAAAGGTAATATTGAATATTTGACACTTGGTAAAAGGTGAACTAC A T KLHL23 Ensembl:ENSG00000213160 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10164599 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26477881 40228 RMVar_ID_40228 Human_SNP_ID_101515266 A-to-I Human chr2 + 169752759 169752759 169752759 TGAAGTCACTGCGGTATGATGAAAAATATTTTACTAAGGCCAAACATTTTAGTAATCCCAGCCTG TGAAGTCACTGCGGTATGATGAAAAATATTTTGCTAAGGCCAAACATTTTAGTAATCCCAGCCTG A G KLHL23 Ensembl:ENSG00000213160 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10171909 Functional Loss SNV dbSNP153 33..33 33 - - - 40229 RMVar_ID_40229 Human_SNP_ID_101515267 A-to-I Human chr2 + 169752759 169752759 169752759 TGAAGTCACTGCGGTATGATGAAAAATATTTTACTAAGGCCAAACATTTTAGTAATCCCAGCCTG TGAAGTCACTGCGGTATGATGAAAAATATTTTTCTAAGGCCAAACATTTTAGTAATCCCAGCCTG A T KLHL23 Ensembl:ENSG00000213160 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10171909 Functional Loss SNV dbSNP153 33..33 33 - - - 40230 RMVar_ID_40230 Human_SNP_ID_101516128 A-to-I Human chr2 + 169754454 169754454 169754454 TGGAGTGCAGTGGTGCAATCTCGGCTCACTGCAACCTCCGCCTCCCCGATTCAAGGGATTCTCCT TGGAGTGCAGTGGTGCAATCTCGGCTCACTGCCACCTCCGCCTCCCCGATTCAAGGGATTCTCCT A C KLHL23 Ensembl:ENSG00000213160 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1191473279 Functional Loss SNV dbSNP153 33..33 33 - - - 40231 RMVar_ID_40231 Human_SNP_ID_101528667 A-to-I Human chr2 + 169804578 169804578 169804578 GCCCCCCACCCCCTTTTTTGAGATGGAGTCTCACTCTTTTGTCAGGCTGGAATGCAGTGGCACAA GCCCCCCACCCCCTTTTTTGAGATGGAGTCTCTCTCTTTTGTCAGGCTGGAATGCAGTGGCACAA A T SSB Ensembl:ENSG00000138385 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1330211127 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 40232 RMVar_ID_40232 Human_SNP_ID_101528679 A-to-I Human chr2 + 169804620 169804620 169804620 CAGGCTGGAATGCAGTGGCACAATCTTGGCTCACTGCAGCCTCTGCCTCCCGGTTTCAAATGATT CAGGCTGGAATGCAGTGGCACAATCTTGGCTCTCTGCAGCCTCTGCCTCCCGGTTTCAAATGATT A T SSB Ensembl:ENSG00000138385 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1250356202 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 40233 RMVar_ID_40233 Human_SNP_ID_101531131 A-to-I Human chr2 - 169813330 169813330 169813330 GGTCAGGAGATCAAGACCATCCTGGCTAACATAGTGAAACCCTGTCTCTACTAAAAAATACCAAA GGTCAGGAGATCAAGACCATCCTGGCTAACATCGTGAAACCCTGTCTCTACTAAAAAATACCAAA T G METTL5 Ensembl:ENSG00000138382 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1488355264 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_338296 40234 RMVar_ID_40234 Human_SNP_ID_101531136 A-to-I Human chr2 - 169813350 169813350 169813350 CTGAGGTGGGCAGATCTTGAGGTCAGGAGATCAAGACCATCCTGGCTAACATAGTGAAACCCTGT CTGAGGTGGGCAGATCTTGAGGTCAGGAGATCGAGACCATCCTGGCTAACATAGTGAAACCCTGT T C METTL5 Ensembl:ENSG00000138382 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs559413013 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_338296 40235 RMVar_ID_40235 Human_SNP_ID_101531389 A-to-I Human chr2 - 169814359 169814359 169814359 CCTCAGTCTCCCAAATAGTTGGGACTACAGGCATGCACTACCACGCCCGGCTAATTTTTTAATCT CCTCAGTCTCCCAAATAGTTGGGACTACAGGCGTGCACTACCACGCCCGGCTAATTTTTTAATCT T C METTL5 Ensembl:ENSG00000138382 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs74618359 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_338296 40236 RMVar_ID_40236 Human_SNP_ID_101531412 A-to-I Human chr2 - 169814447 169814446 169814447 TTTTTTTTTTTGAGACAAAGCCTTGCTCTGTTACCCAGGCTGGAGTGCAGTGGCAACCTCCACCT TTTTTTTTTTTGAGACAAAGCCTTGCTCTGTT_CCCAGGCTGGAGTGCAGTGGCAACCTCCACCT GT G METTL5 Ensembl:ENSG00000138382 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1341620094 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_338296 40237 RMVar_ID_40237 Human_SNP_ID_101531651 A-to-I Human chr2 - 169815029 169815029 169815029 AAATTAGCCAGGCATGGTGGCGCACACGTGTAATCTCAGCTACTTGGGAGACTGAGGCGGGAGAA AAATTAGCCAGGCATGGTGGCGCACACGTGTATTCTCAGCTACTTGGGAGACTGAGGCGGGAGAA T A METTL5 Ensembl:ENSG00000138382 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1166897801 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_338296 40238 RMVar_ID_40238 Human_SNP_ID_101531666 A-to-I Human chr2 - 169815094 169815084 169815094 GAGGTTTGGAGCTCAAGACCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATATAAA GAGGTTTGGAGCTCAAGACCAGCCTGGCCAAC__________CCCATCTCTACTAAAAATATAAA GGTTTCACCAT G METTL5 Ensembl:ENSG00000138382 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1306188265 Functional Loss DEL dbSNP153 33..42 33 - - - RMVar_hsa_circ_338296 40239 RMVar_ID_40239 Human_SNP_ID_101533801 A-to-I Human chr2 - 169823637 169823637 169823637 TTTTTTATTTTTTGTAGAGACAGCGTCTTGCTATGTTGCCCAAGATGGTCTCAGACTCCTGGGCT TTTTTTATTTTTTGTAGAGACAGCGTCTTGCTGTGTTGCCCAAGATGGTCTCAGACTCCTGGGCT T C METTL5 Ensembl:ENSG00000138382 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs965076320 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25479879 40240 RMVar_ID_40240 Human_SNP_ID_101542056 A-to-I Human chr2 + 169852796 169852796 169852796 TGGCTTGAACCCAGTGGGTGGAGGTTGCAGTGAGCGGAGATCACACCACTTCACTCCAGCCTGGG TGGCTTGAACCCAGTGGGTGGAGGTTGCAGTGCGCGGAGATCACACCACTTCACTCCAGCCTGGG A C UBR3 Ensembl:ENSG00000144357 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1304262558 Functional Loss SNV dbSNP153 33..33 33 - - - 40241 RMVar_ID_40241 Human_SNP_ID_101542059 A-to-I Human chr2 + 169852806 169852806 169852806 CCAGTGGGTGGAGGTTGCAGTGAGCGGAGATCACACCACTTCACTCCAGCCTGGGTGAAAGAGTG CCAGTGGGTGGAGGTTGCAGTGAGCGGAGATCCCACCACTTCACTCCAGCCTGGGTGAAAGAGTG A C UBR3 Ensembl:ENSG00000144357 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs189200716 Functional Loss SNV dbSNP153 33..33 33 - - - 40242 RMVar_ID_40242 Human_SNP_ID_101553141 A-to-I Human chr2 + 169894200 169894200 169894200 AATAAATTAGCAGGGTGTGGTCTTGCACACCTATAGTCCTAGCTATTCGGGAGGGTAAGGTGGGA AATAAATTAGCAGGGTGTGGTCTTGCACACCTGTAGTCCTAGCTATTCGGGAGGGTAAGGTGGGA A G UBR3 Ensembl:ENSG00000144357 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1371043119 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25410,RMVar_hsa_circ_12412,RMVar_hsa_circ_44133,RMVar_hsa_circ_289520,RMVar_hsa_circ_296561,RMVar_hsa_circ_330393,RMVar_hsa_circ_330164,RMVar_hsa_circ_280493,RMVar_hsa_circ_23141,RMVar_hsa_circ_42639,RMVar_hsa_circ_44521,RMVar_hsa_circ_204479,RMVar_hsa_circ_204481,RMVar_hsa_circ_204482,RMVar_hsa_circ_204483,RMVar_hsa_circ_204480,RMVar_hsa_circ_204478,RMVar_hsa_circ_112467,RMVar_hsa_circ_204484,RMVar_hsa_circ_115786,RMVar_hsa_circ_50103,RMVar_hsa_circ_204486,RMVar_hsa_circ_204485,RMVar_hsa_circ_86318,RMVar_hsa_circ_30912,RMVar_hsa_circ_15515,RMVar_hsa_circ_54212,RMVar_hsa_circ_105610,RMVar_hsa_circ_204489,RMVar_hsa_circ_9128,RMVar_hsa_circ_315577,RMVar_hsa_circ_312096,RMVar_hsa_circ_91478,RMVar_hsa_circ_204491,RMVar_hsa_circ_204492,RMVar_hsa_circ_204493,RMVar_hsa_circ_333841,RMVar_hsa_circ_334678,RMVar_hsa_circ_289165,RMVar_hsa_circ_61312,RMVar_hsa_circ_72304,RMVar_hsa_circ_48148,RMVar_hsa_circ_204495,RMVar_hsa_circ_15241,RMVar_hsa_circ_204496,RMVar_hsa_circ_204494 40243 RMVar_ID_40243 Human_SNP_ID_101561628 A-to-I Human chr2 + 169930461 169930461 169930461 CAGGCTGGAGTGCAGTGGCGCCATCATAGCTCACTGCACCCTTGACCTACTGGGCTCAAGTGGTC CAGGCTGGAGTGCAGTGGCGCCATCATAGCTCTCTGCACCCTTGACCTACTGGGCTCAAGTGGTC A T UBR3 Ensembl:ENSG00000144357 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1011781189 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6685,RMVar_hsa_circ_12412,RMVar_hsa_circ_44133,RMVar_hsa_circ_330164,RMVar_hsa_circ_42639,RMVar_hsa_circ_44521,RMVar_hsa_circ_204482,RMVar_hsa_circ_204483,RMVar_hsa_circ_115786,RMVar_hsa_circ_204485,RMVar_hsa_circ_30912,RMVar_hsa_circ_105610,RMVar_hsa_circ_91478,RMVar_hsa_circ_204493,RMVar_hsa_circ_61312,RMVar_hsa_circ_72304,RMVar_hsa_circ_204496,RMVar_hsa_circ_75857,RMVar_hsa_circ_43076,RMVar_hsa_circ_52762,RMVar_hsa_circ_69894,RMVar_hsa_circ_204497,RMVar_hsa_circ_368553,RMVar_hsa_circ_353704,RMVar_hsa_circ_341054,RMVar_hsa_circ_72392,RMVar_hsa_circ_74228,RMVar_hsa_circ_378072,RMVar_hsa_circ_321251,RMVar_hsa_circ_345604,RMVar_hsa_circ_330100,RMVar_hsa_circ_307924,RMVar_hsa_circ_316251,RMVar_hsa_circ_32938,RMVar_hsa_circ_204507,RMVar_hsa_circ_204508,RMVar_hsa_circ_204506,RMVar_hsa_circ_74960,RMVar_hsa_circ_43022,RMVar_hsa_circ_288561,RMVar_hsa_circ_55969,RMVar_hsa_circ_47338,RMVar_hsa_circ_204513,RMVar_hsa_circ_340144,RMVar_hsa_circ_72264,RMVar_hsa_circ_71994 40244 RMVar_ID_40244 Human_SNP_ID_101583698 A-to-I Human chr2 + 170024130 170024130 170024130 TTAGAAATAACTGACAGAGGGCTGAGGTGGGCAGATTACGAGGTCAGGAGATCGAGACCATCCTG TTAGAAATAACTGACAGAGGGCTGAGGTGGGCGGATTACGAGGTCAGGAGATCGAGACCATCCTG A G UBR3 Ensembl:ENSG00000144357 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1393078238 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6685,RMVar_hsa_circ_44133,RMVar_hsa_circ_42639,RMVar_hsa_circ_105610,RMVar_hsa_circ_204493,RMVar_hsa_circ_47338,RMVar_hsa_circ_76615,RMVar_hsa_circ_204517,RMVar_hsa_circ_64273,RMVar_hsa_circ_17532,RMVar_hsa_circ_284034,RMVar_hsa_circ_304107,RMVar_hsa_circ_277931,RMVar_hsa_circ_29434,RMVar_hsa_circ_336335,RMVar_hsa_circ_204519,RMVar_hsa_circ_204520,RMVar_hsa_circ_378000,RMVar_hsa_circ_330386,RMVar_hsa_circ_54747,RMVar_hsa_circ_360173,RMVar_hsa_circ_360556,RMVar_hsa_circ_323108,RMVar_hsa_circ_312412,RMVar_hsa_circ_323178,RMVar_hsa_circ_266260,RMVar_hsa_circ_71190,RMVar_hsa_circ_204528,RMVar_hsa_circ_204529,RMVar_hsa_circ_363904,RMVar_hsa_circ_67565,RMVar_hsa_circ_17002,RMVar_hsa_circ_34945,RMVar_hsa_circ_354781,RMVar_hsa_circ_339926,RMVar_hsa_circ_20642,RMVar_hsa_circ_204538,RMVar_hsa_circ_204533,RMVar_hsa_circ_204531,RMVar_hsa_circ_302337,RMVar_hsa_circ_366266,RMVar_hsa_circ_204532,RMVar_hsa_circ_361945,RMVar_hsa_circ_337482,RMVar_hsa_circ_296025,RMVar_hsa_circ_310917,RMVar_hsa_circ_204534,RMVar_hsa_circ_34488,RMVar_hsa_circ_204535,RMVar_hsa_circ_289327,RMVar_hsa_circ_322524,RMVar_hsa_circ_335397,RMVar_hsa_circ_204536,RMVar_hsa_circ_69691,RMVar_hsa_circ_278774,RMVar_hsa_circ_348213,RMVar_hsa_circ_362149,RMVar_hsa_circ_366450,RMVar_hsa_circ_328646,RMVar_hsa_circ_204540,RMVar_hsa_circ_274557,RMVar_hsa_circ_204539,RMVar_hsa_circ_204537 40245 RMVar_ID_40245 Human_SNP_ID_101593679 A-to-I Human chr2 + 170067839 170067839 170067839 TTGCCCAGGCTCGAGGGCAGTGGTGTGATCTCAGCTGACTGCAACCTCTGCACCTGGGTTCAAGC TTGCCCAGGCTCGAGGGCAGTGGTGTGATCTCTGCTGACTGCAACCTCTGCACCTGGGTTCAAGC A T UBR3 Ensembl:ENSG00000144357 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388974272 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105610,RMVar_hsa_circ_204493,RMVar_hsa_circ_11088,RMVar_hsa_circ_336335,RMVar_hsa_circ_323108,RMVar_hsa_circ_67565,RMVar_hsa_circ_362149,RMVar_hsa_circ_366450,RMVar_hsa_circ_341143,RMVar_hsa_circ_204543,RMVar_hsa_circ_339389,RMVar_hsa_circ_61374,RMVar_hsa_circ_350430 40246 RMVar_ID_40246 Human_SNP_ID_101760930 A-to-I Human chr2 + 170752506 170752506 170752506 CATCGTCAACCCAAACATCTCCTTGCATTTTTATTGGCTGAATTGGGTACAAGTGGTTCTATAGA CATCGTCAACCCAAACATCTCCTTGCATTTTTGTTGGCTGAATTGGGTACAAGTGGTTCTATAGA A G EIF2S2P4 Ensembl:ENSG00000128692 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879177767 Functional Loss SNV dbSNP153 33..33 33 - - - 40247 RMVar_ID_40247 Human_SNP_ID_101766233 A-to-I Human chr2 + 170775171 170775171 170775171 AAAGGTGGGCCAGGAAGGTGGCTCACGCCTGCAATCCCAGCACTTTGGGAGGCCCAGGCAGGAGG AAAGGTGGGCCAGGAAGGTGGCTCACGCCTGCGATCCCAGCACTTTGGGAGGCCCAGGCAGGAGG A G AC007405.4 Ensembl:ENSG00000239467 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs957924638 Functional Loss SNV dbSNP153 33..33 33 - - - 40248 RMVar_ID_40248 Human_SNP_ID_101789164 A-to-I Human chr2 + 170870421 170870421 170870421 CACCACGCCCGGCTGGTTTTTGTATTTTTAGTAGAGACGGGATTTCACCATGTTGGTCAGGCTGG CACCACGCCCGGCTGGTTTTTGTATTTTTAGTGGAGACGGGATTTCACCATGTTGGTCAGGCTGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1028763463 Functional Loss SNV dbSNP153 33..33 33 - - - 40249 RMVar_ID_40249 Human_SNP_ID_101807348 A-to-I Human chr2 + 170946208 170946208 170946208 TAATTTTTTTGTAGAAACAGGGGTCTCCCTATATTGCCCAGGCTAGTCTCAAACTCCTGGACTCC TAATTTTTTTGTAGAAACAGGGGTCTCCCTATGTTGCCCAGGCTAGTCTCAAACTCCTGGACTCC A G GORASP2 Ensembl:ENSG00000115806 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965530413 Functional Loss SNV dbSNP153 33..33 33 - - - 40250 RMVar_ID_40250 Human_SNP_ID_101807349 A-to-I Human chr2 + 170946208 170946208 170946208 TAATTTTTTTGTAGAAACAGGGGTCTCCCTATATTGCCCAGGCTAGTCTCAAACTCCTGGACTCC TAATTTTTTTGTAGAAACAGGGGTCTCCCTATTTTGCCCAGGCTAGTCTCAAACTCCTGGACTCC A T GORASP2 Ensembl:ENSG00000115806 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965530413 Functional Loss SNV dbSNP153 33..33 33 - - - 40251 RMVar_ID_40251 Human_SNP_ID_101808945 A-to-I Human chr2 + 170952745 170952745 170952745 GCGTCTTGCTCTCTGGGCTGGAGCACAATCATAGTTCACTGCAGCCTTTAACTCCTGGGCTCAAG GCGTCTTGCTCTCTGGGCTGGAGCACAATCATGGTTCACTGCAGCCTTTAACTCCTGGGCTCAAG A G GORASP2 Ensembl:ENSG00000115806 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs896833722 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21348,RMVar_hsa_circ_345410,RMVar_hsa_circ_351567,RMVar_hsa_circ_43740,RMVar_hsa_circ_204571,RMVar_hsa_circ_204572,RMVar_hsa_circ_204574,RMVar_hsa_circ_313000 40252 RMVar_ID_40252 Human_SNP_ID_101808947 A-to-I Human chr2 + 170952755 170952755 170952755 CTCTGGGCTGGAGCACAATCATAGTTCACTGCAGCCTTTAACTCCTGGGCTCAAGCTGTCCTCCC CTCTGGGCTGGAGCACAATCATAGTTCACTGCCGCCTTTAACTCCTGGGCTCAAGCTGTCCTCCC A C GORASP2 Ensembl:ENSG00000115806 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1182657314 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21348,RMVar_hsa_circ_345410,RMVar_hsa_circ_351567,RMVar_hsa_circ_43740,RMVar_hsa_circ_204571,RMVar_hsa_circ_204572,RMVar_hsa_circ_204574,RMVar_hsa_circ_313000 40253 RMVar_ID_40253 Human_SNP_ID_101808982 A-to-I Human chr2 + 170952910 170952910 170952910 GTTTCCCAGGCTAGTCTTGAACTCTTCGCTTCAAGCAATCTTCCCACCTTGGCCTCCCAAAGTCC GTTTCCCAGGCTAGTCTTGAACTCTTCGCTTCGAGCAATCTTCCCACCTTGGCCTCCCAAAGTCC A G GORASP2 Ensembl:ENSG00000115806 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1220377436 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21348,RMVar_hsa_circ_345410,RMVar_hsa_circ_351567,RMVar_hsa_circ_43740,RMVar_hsa_circ_204571,RMVar_hsa_circ_204572,RMVar_hsa_circ_204574,RMVar_hsa_circ_313000 40254 RMVar_ID_40254 Human_SNP_ID_101809047 A-to-I Human chr2 + 170953233 170953233 170953233 CAAAAATTAGCCAGATGTGGTGGCATGCACCTATAGTCCCAGCTACTCAGGAGGCTCAGGCGGGA CAAAAATTAGCCAGATGTGGTGGCATGCACCTGTAGTCCCAGCTACTCAGGAGGCTCAGGCGGGA A G GORASP2 Ensembl:ENSG00000115806 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs147401872 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21348,RMVar_hsa_circ_345410,RMVar_hsa_circ_351567,RMVar_hsa_circ_43740,RMVar_hsa_circ_204571,RMVar_hsa_circ_204572,RMVar_hsa_circ_204574,RMVar_hsa_circ_313000 40255 RMVar_ID_40255 Human_SNP_ID_101810181 A-to-I Human chr2 + 170957844 170957844 170957844 TTTTTCTGAAGTTTTAGTTTTTATGTTTTTGTAGGGCTGGGGTCTCTCTGTTGCCCAGGCTGGTC TTTTTCTGAAGTTTTAGTTTTTATGTTTTTGTGGGGCTGGGGTCTCTCTGTTGCCCAGGCTGGTC A G GORASP2 Ensembl:ENSG00000115806 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs921322749 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_775349,Human_RBP_ID_6848561,Human_RBP_ID_13674311 RMVar_hsa_circ_345410,RMVar_hsa_circ_204572,RMVar_hsa_circ_204576,RMVar_hsa_circ_375050,RMVar_hsa_circ_30684 40256 RMVar_ID_40256 Human_SNP_ID_101811448 A-to-I Human chr2 + 170962889 170962889 170962889 CAGGACTGCCCAACCTCCCCAACCTCAACCTCAACCTCCCAGCACCACACATCATGCCAGGGGTT CAGGACTGCCCAACCTCCCCAACCTCAACCTCTACCTCCCAGCACCACACATCATGCCAGGGGTT A T GORASP2 Ensembl:ENSG00000115806 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs145218389 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_775350,Human_RBP_ID_17274064,Human_RBP_ID_17389294,Human_RBP_ID_17510157,Human_RBP_ID_17697627,Human_RBP_ID_17943599,Human_RBP_ID_18948381,Human_RBP_ID_27475762 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 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 40257 RMVar_ID_40257 Human_SNP_ID_101811548 A-to-I Human chr2 + 170963283 170963280 170963283 TGTAGTCCCAGCTACGCAGGAGGCTGAGACAGAAGAATCACTTGAACCCAGGAGGTGGAGGTTGC TGTAGTCCCAGCTACGCAGGAGGCTGAGAC___AGAATCACTTGAACCCAGGAGGTGGAGGTTGC CAGA C GORASP2 Ensembl:ENSG00000115806 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs779844930 Functional Loss DEL dbSNP153 31..33 33 - - - RMVar_hsa_circ_89579,RMVar_hsa_circ_204578 40258 RMVar_ID_40258 Human_SNP_ID_101811549 A-to-I Human chr2 + 170963300 170963300 170963300 AGGAGGCTGAGACAGAAGAATCACTTGAACCCAGGAGGTGGAGGTTGCAATGAGCTGAGATCACA AGGAGGCTGAGACAGAAGAATCACTTGAACCCCGGAGGTGGAGGTTGCAATGAGCTGAGATCACA A C GORASP2 Ensembl:ENSG00000115806 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1371883362 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89579,RMVar_hsa_circ_204578 40259 RMVar_ID_40259 Human_SNP_ID_101811721 A-to-I Human chr2 + 170963665 170963664 170963666 GTATTTTTTGTTTTGTTTAGTTTTTTTGAGACAGAGTCTTGCTTTATCACCCAGGCTGGAGTGCA GTATTTTTTGTTTTGTTTAGTTTTTTTGAGAC__AGTCTTGCTTTATCACCCAGGCTGGAGTGCA CAG C GORASP2 Ensembl:ENSG00000115806 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1005805068 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_17570034 RMVar_hsa_circ_89579,RMVar_hsa_circ_204578 40260 RMVar_ID_40260 Human_SNP_ID_101811722 A-to-I Human chr2 + 170963665 170963665 170963665 GTATTTTTTGTTTTGTTTAGTTTTTTTGAGACAGAGTCTTGCTTTATCACCCAGGCTGGAGTGCA GTATTTTTTGTTTTGTTTAGTTTTTTTGAGACGGAGTCTTGCTTTATCACCCAGGCTGGAGTGCA A G GORASP2 Ensembl:ENSG00000115806 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1036454152 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17570034 RMVar_hsa_circ_89579,RMVar_hsa_circ_204578 40261 RMVar_ID_40261 Human_SNP_ID_101811906 A-to-I Human chr2 + 170964395 170964395 170964395 AAGTACTAGGCCAGGCACAGTGGCTCACGCCTATAATGCCAGCACTTTGGGAAGCCAAGGTGGGT AAGTACTAGGCCAGGCACAGTGGCTCACGCCTCTAATGCCAGCACTTTGGGAAGCCAAGGTGGGT A C GORASP2 Ensembl:ENSG00000115806 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1347154540 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89579,RMVar_hsa_circ_204578 40262 RMVar_ID_40262 Human_SNP_ID_101811927 A-to-I Human chr2 + 170964514 170964514 170964514 GTCTCTATTAAAAATAGAAAAAGTAGCTGGGCATGGTGGCAGGTGCATGTAATCCCAGCTACTCG GTCTCTATTAAAAATAGAAAAAGTAGCTGGGCGTGGTGGCAGGTGCATGTAATCCCAGCTACTCG A G GORASP2 Ensembl:ENSG00000115806 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs938442279 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89579,RMVar_hsa_circ_204578 40263 RMVar_ID_40263 Human_SNP_ID_101811959 A-to-I Human chr2 + 170964635 170964635 170964635 AGGTCGCACCACTGCACTCCAGCCTGGGTGACAGAATGAGACTCCGTCTCAAAAAAAAATAAAAA AGGTCGCACCACTGCACTCCAGCCTGGGTGACGGAATGAGACTCCGTCTCAAAAAAAAATAAAAA A G GORASP2 Ensembl:ENSG00000115806 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs141512479 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89579,RMVar_hsa_circ_204578 40264 RMVar_ID_40264 Human_SNP_ID_101819956 A-to-I Human chr2 - 170990407 170990407 170990407 AAATTAGCTGGGCATGGTGGTGCATACCTGTAATCTCAGCTACTCAGGAGGCTGAGGCAGGATAG AAATTAGCTGGGCATGGTGGTGCATACCTGTAGTCTCAGCTACTCAGGAGGCTGAGGCAGGATAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs571164956 Functional Loss SNV dbSNP153 33..33 33 - - - 40265 RMVar_ID_40265 Human_SNP_ID_101819968 A-to-I Human chr2 - 170990448 170990447 170990448 GACCAACATGGTGAAACCCCATCTCTACTAAAAGTACAAAAAAATTAGCTGGGCATGGTGGTGCA GACCAACATGGTGAAACCCCATCTCTACTAAA_GTACAAAAAAATTAGCTGGGCATGGTGGTGCA CT C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1411615167 Functional Loss DEL dbSNP153 33..33 33 - - - 40266 RMVar_ID_40266 Human_SNP_ID_101822300 A-to-I Human chr2 - 170999060 170999060 170999060 CCCTTCATCTATTAAAAATTATGAACTGGCTTAGTGTGGTGGCTCATGCCTGTAATCCTAGCACT CCCTTCATCTATTAAAAATTATGAACTGGCTTCGTGTGGTGGCTCATGCCTGTAATCCTAGCACT T G TLK1 Ensembl:ENSG00000198586 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1287250725 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111553,RMVar_hsa_circ_127504,RMVar_hsa_circ_367800,RMVar_hsa_circ_204579,RMVar_hsa_circ_204580 40267 RMVar_ID_40267 Human_SNP_ID_101822637 A-to-I Human chr2 - 171000296 171000296 171000296 TGGTTCACTGCAACCTCTGCCTCCCAGGTTCAAGCGATTTCTCCTGCCTCAGCCTCCCAAGTAGT TGGTTCACTGCAACCTCTGCCTCCCAGGTTCATGCGATTTCTCCTGCCTCAGCCTCCCAAGTAGT T A TLK1 Ensembl:ENSG00000198586 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1413450562 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111553,RMVar_hsa_circ_127504,RMVar_hsa_circ_367800,RMVar_hsa_circ_204579,RMVar_hsa_circ_204580 40268 RMVar_ID_40268 Human_SNP_ID_101822646 A-to-I Human chr2 - 171000335 171000335 171000335 TCGCTCTGTCACCCAGGCTGCAGTGCAATGGCACAGTCTTGGTTCACTGCAACCTCTGCCTCCCA TCGCTCTGTCACCCAGGCTGCAGTGCAATGGCGCAGTCTTGGTTCACTGCAACCTCTGCCTCCCA T C TLK1 Ensembl:ENSG00000198586 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1368523460 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111553,RMVar_hsa_circ_127504,RMVar_hsa_circ_367800,RMVar_hsa_circ_204579,RMVar_hsa_circ_204580 40269 RMVar_ID_40269 Human_SNP_ID_101823087 A-to-I Human chr2 - 171001909 171001909 171001909 GGGTGTGGTGGTGCATGCCTGTATTCTCAGCTACTATGGAGGCTGAGGCAGGAGAATTGCTTGAA GGGTGTGGTGGTGCATGCCTGTATTCTCAGCTGCTATGGAGGCTGAGGCAGGAGAATTGCTTGAA T C TLK1 Ensembl:ENSG00000198586 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1428615573 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111553,RMVar_hsa_circ_127504,RMVar_hsa_circ_367800,RMVar_hsa_circ_204579,RMVar_hsa_circ_204580 40270 RMVar_ID_40270 Human_SNP_ID_101823259 A-to-I Human chr2 - 171002553 171002553 171002553 TTAGAAAAAGCAGGCCAGGCGCGGTGGCTCACACCTATAATCCCAGCACTTTGGGAGGCCGAGGC TTAGAAAAAGCAGGCCAGGCGCGGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCCGAGGC T C TLK1 Ensembl:ENSG00000198586 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1479230616 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111553,RMVar_hsa_circ_127504,RMVar_hsa_circ_367800,RMVar_hsa_circ_204579,RMVar_hsa_circ_204580 40271 RMVar_ID_40271 Human_SNP_ID_101823327 A-to-I Human chr2 - 171002773 171002773 171002773 AAATTAGCCAAATGTGGTGGCACACACCTGTAATCCCAGCTACACAGGAGGCTGAGACAAGAGGA AAATTAGCCAAATGTGGTGGCACACACCTGTATTCCCAGCTACACAGGAGGCTGAGACAAGAGGA T A TLK1 Ensembl:ENSG00000198586 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1417044881 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111553,RMVar_hsa_circ_127504,RMVar_hsa_circ_367800,RMVar_hsa_circ_204579,RMVar_hsa_circ_204580 40272 RMVar_ID_40272 Human_SNP_ID_101823731 A-to-I Human chr2 - 171004047 171004047 171004047 GGGAGGCTGAGGCAGGGGAATTGTTTGAATCCAGGAGGCAGAGGTTGCAGTGAGCTGAGATCATA GGGAGGCTGAGGCAGGGGAATTGTTTGAATCCGGGAGGCAGAGGTTGCAGTGAGCTGAGATCATA T C TLK1 Ensembl:ENSG00000198586 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1289621618 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111553,RMVar_hsa_circ_127504,RMVar_hsa_circ_367800,RMVar_hsa_circ_204579,RMVar_hsa_circ_204580 40273 RMVar_ID_40273 Human_SNP_ID_101823741 A-to-I Human chr2 - 171004083 171004083 171004083 TGGGCATGGTGGCCATGCCTGGAATCCCAGCTACTTGGGAGGCTGAGGCAGGGGAATTGTTTGAA TGGGCATGGTGGCCATGCCTGGAATCCCAGCTCCTTGGGAGGCTGAGGCAGGGGAATTGTTTGAA T G TLK1 Ensembl:ENSG00000198586 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs368499888 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1193726 RMVar_hsa_circ_111553,RMVar_hsa_circ_127504,RMVar_hsa_circ_367800,RMVar_hsa_circ_204579,RMVar_hsa_circ_204580 40274 RMVar_ID_40274 Human_SNP_ID_101824116 A-to-I Human chr2 - 171005619 171005618 171005619 AAGCGATCTGCCCACTTACTCTTGAGTAACTGAGACCACAGGTACGCACCACTATGCCCAGCTAA AAGCGATCTGCCCACTTACTCTTGAGTAACTG_GACCACAGGTACGCACCACTATGCCCAGCTAA CT C TLK1 Ensembl:ENSG00000198586 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1457012977 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_111553,RMVar_hsa_circ_127504,RMVar_hsa_circ_367800,RMVar_hsa_circ_204579,RMVar_hsa_circ_204580 40275 RMVar_ID_40275 Human_SNP_ID_101824123 A-to-I Human chr2 - 171005657 171005657 171005657 GTAATCTTAGTTCATTGCAGCCTCAAACTCCTAGGCTCAAGCGATCTGCCCACTTACTCTTGAGT GTAATCTTAGTTCATTGCAGCCTCAAACTCCTGGGCTCAAGCGATCTGCCCACTTACTCTTGAGT T C TLK1 Ensembl:ENSG00000198586 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs561944334 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111553,RMVar_hsa_circ_127504,RMVar_hsa_circ_367800,RMVar_hsa_circ_204579,RMVar_hsa_circ_204580 40276 RMVar_ID_40276 Human_SNP_ID_101824124 A-to-I Human chr2 - 171005657 171005657 171005657 GTAATCTTAGTTCATTGCAGCCTCAAACTCCTAGGCTCAAGCGATCTGCCCACTTACTCTTGAGT GTAATCTTAGTTCATTGCAGCCTCAAACTCCTCGGCTCAAGCGATCTGCCCACTTACTCTTGAGT T G TLK1 Ensembl:ENSG00000198586 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs561944334 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111553,RMVar_hsa_circ_127504,RMVar_hsa_circ_367800,RMVar_hsa_circ_204579,RMVar_hsa_circ_204580 40277 RMVar_ID_40277 Human_SNP_ID_101824127 A-to-I Human chr2 - 171005664 171005664 171005664 CAGTGGTGTAATCTTAGTTCATTGCAGCCTCAAACTCCTAGGCTCAAGCGATCTGCCCACTTACT CAGTGGTGTAATCTTAGTTCATTGCAGCCTCAGACTCCTAGGCTCAAGCGATCTGCCCACTTACT T C TLK1 Ensembl:ENSG00000198586 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs574121587 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111553,RMVar_hsa_circ_127504,RMVar_hsa_circ_367800,RMVar_hsa_circ_204579,RMVar_hsa_circ_204580 40278 RMVar_ID_40278 Human_SNP_ID_101824137 A-to-I Human chr2 - 171005727 171005727 171005727 TCTGTGGAGGTTATATGGTTGCAGGAATTTTCATTTTATTTTGAGACAGGGTCTTGCCCTGTGCA TCTGTGGAGGTTATATGGTTGCAGGAATTTTCTTTTTATTTTGAGACAGGGTCTTGCCCTGTGCA T A TLK1 Ensembl:ENSG00000198586 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6433275 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13674923 RMVar_hsa_circ_111553,RMVar_hsa_circ_127504,RMVar_hsa_circ_367800,RMVar_hsa_circ_204579,RMVar_hsa_circ_204580 40279 RMVar_ID_40279 Human_SNP_ID_101824138 A-to-I Human chr2 - 171005727 171005727 171005727 TCTGTGGAGGTTATATGGTTGCAGGAATTTTCATTTTATTTTGAGACAGGGTCTTGCCCTGTGCA TCTGTGGAGGTTATATGGTTGCAGGAATTTTCGTTTTATTTTGAGACAGGGTCTTGCCCTGTGCA T C TLK1 Ensembl:ENSG00000198586 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6433275 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13674923 RMVar_hsa_circ_111553,RMVar_hsa_circ_127504,RMVar_hsa_circ_367800,RMVar_hsa_circ_204579,RMVar_hsa_circ_204580 40280 RMVar_ID_40280 Human_SNP_ID_101824139 A-to-I Human chr2 - 171005727 171005727 171005727 TCTGTGGAGGTTATATGGTTGCAGGAATTTTCATTTTATTTTGAGACAGGGTCTTGCCCTGTGCA TCTGTGGAGGTTATATGGTTGCAGGAATTTTCCTTTTATTTTGAGACAGGGTCTTGCCCTGTGCA T G TLK1 Ensembl:ENSG00000198586 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6433275 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13674923 RMVar_hsa_circ_111553,RMVar_hsa_circ_127504,RMVar_hsa_circ_367800,RMVar_hsa_circ_204579,RMVar_hsa_circ_204580 40281 RMVar_ID_40281 Human_SNP_ID_101828304 A-to-I Human chr2 - 171021935 171021935 171021935 CCATGCCTGGCTAATTTTTATATATATTTTTTAGTAGAAACGGGGTTTCACCATGTTGGTCAGGC CCATGCCTGGCTAATTTTTATATATATTTTTTCGTAGAAACGGGGTTTCACCATGTTGGTCAGGC T G TLK1 Ensembl:ENSG00000198586 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1169034190 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23836494 RMVar_hsa_circ_64591,RMVar_hsa_circ_111553,RMVar_hsa_circ_282102,RMVar_hsa_circ_127504,RMVar_hsa_circ_204579,RMVar_hsa_circ_377482,RMVar_hsa_circ_204580,RMVar_hsa_circ_332004,RMVar_hsa_circ_309751,RMVar_hsa_circ_281803,RMVar_hsa_circ_204584,RMVar_hsa_circ_62983,RMVar_hsa_circ_41284,RMVar_hsa_circ_204585,RMVar_hsa_circ_204583,RMVar_hsa_circ_127448,RMVar_hsa_circ_367091,RMVar_hsa_circ_204586,RMVar_hsa_circ_51473,RMVar_hsa_circ_54659,RMVar_hsa_circ_63797,RMVar_hsa_circ_355561,RMVar_hsa_circ_367869,RMVar_hsa_circ_330928,RMVar_hsa_circ_298914,RMVar_hsa_circ_204588,RMVar_hsa_circ_204589,RMVar_hsa_circ_314262,RMVar_hsa_circ_361633,RMVar_hsa_circ_305422,RMVar_hsa_circ_204590,RMVar_hsa_circ_32620 40282 RMVar_ID_40282 Human_SNP_ID_101833072 A-to-I Human chr2 - 171040725 171040725 171040725 CAAAAAATAAAAAATTAGCCAGACATGGTGGTATGTACCTATAGTCCCAGCTTCTCAGGAGGCTG CAAAAAATAAAAAATTAGCCAGACATGGTGGTGTGTACCTATAGTCCCAGCTTCTCAGGAGGCTG T C TLK1 Ensembl:ENSG00000198586 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs951778782 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_361,RMVar_hsa_circ_64591,RMVar_hsa_circ_111553,RMVar_hsa_circ_127504,RMVar_hsa_circ_204579,RMVar_hsa_circ_377482,RMVar_hsa_circ_204580,RMVar_hsa_circ_332004,RMVar_hsa_circ_309751,RMVar_hsa_circ_281803,RMVar_hsa_circ_204584,RMVar_hsa_circ_41284,RMVar_hsa_circ_204585,RMVar_hsa_circ_204583,RMVar_hsa_circ_127448,RMVar_hsa_circ_204586,RMVar_hsa_circ_51473,RMVar_hsa_circ_54659,RMVar_hsa_circ_63797,RMVar_hsa_circ_367869,RMVar_hsa_circ_330928,RMVar_hsa_circ_204589,RMVar_hsa_circ_361633,RMVar_hsa_circ_89870,RMVar_hsa_circ_32620,RMVar_hsa_circ_292229,RMVar_hsa_circ_65337,RMVar_hsa_circ_127131,RMVar_hsa_circ_335533,RMVar_hsa_circ_204593,RMVar_hsa_circ_204594,RMVar_hsa_circ_354329,RMVar_hsa_circ_312978,RMVar_hsa_circ_322046,RMVar_hsa_circ_286628,RMVar_hsa_circ_110598,RMVar_hsa_circ_204597,RMVar_hsa_circ_204598,RMVar_hsa_circ_204596 40283 RMVar_ID_40283 Human_SNP_ID_101840827 A-to-I Human chr2 - 171071566 171071566 171071566 ATGGACAAATGGGGTCAGGCGTGGTGGCTCACACCTGTAATCCCAGCACTGTGGGAGGCAGAGGC ATGGACAAATGGGGTCAGGCGTGGTGGCTCACGCCTGTAATCCCAGCACTGTGGGAGGCAGAGGC T C TLK1 Ensembl:ENSG00000198586 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs200254309 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_377482,RMVar_hsa_circ_309751,RMVar_hsa_circ_204585,RMVar_hsa_circ_127448,RMVar_hsa_circ_204586,RMVar_hsa_circ_367869,RMVar_hsa_circ_89870,RMVar_hsa_circ_65337,RMVar_hsa_circ_27865,RMVar_hsa_circ_127131,RMVar_hsa_circ_204594,RMVar_hsa_circ_354329,RMVar_hsa_circ_312978,RMVar_hsa_circ_204598,RMVar_hsa_circ_343569,RMVar_hsa_circ_322077,RMVar_hsa_circ_359387,RMVar_hsa_circ_54203,RMVar_hsa_circ_320157,RMVar_hsa_circ_364027,RMVar_hsa_circ_361433,RMVar_hsa_circ_204602,RMVar_hsa_circ_108894,RMVar_hsa_circ_352992 40284 RMVar_ID_40284 Human_SNP_ID_101840837 A-to-I Human chr2 - 171071582 171071582 171071582 GCAACCAAAGGTAAAAATGGACAAATGGGGTCAGGCGTGGTGGCTCACACCTGTAATCCCAGCAC GCAACCAAAGGTAAAAATGGACAAATGGGGTCCGGCGTGGTGGCTCACACCTGTAATCCCAGCAC T G TLK1 Ensembl:ENSG00000198586 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs777843525 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_377482,RMVar_hsa_circ_309751,RMVar_hsa_circ_204585,RMVar_hsa_circ_127448,RMVar_hsa_circ_204586,RMVar_hsa_circ_367869,RMVar_hsa_circ_89870,RMVar_hsa_circ_65337,RMVar_hsa_circ_27865,RMVar_hsa_circ_127131,RMVar_hsa_circ_204594,RMVar_hsa_circ_354329,RMVar_hsa_circ_312978,RMVar_hsa_circ_204598,RMVar_hsa_circ_343569,RMVar_hsa_circ_322077,RMVar_hsa_circ_359387,RMVar_hsa_circ_54203,RMVar_hsa_circ_320157,RMVar_hsa_circ_364027,RMVar_hsa_circ_361433,RMVar_hsa_circ_204602,RMVar_hsa_circ_108894,RMVar_hsa_circ_352992 40285 RMVar_ID_40285 Human_SNP_ID_101841136 A-to-I Human chr2 - 171072656 171072656 171072656 TCAAGTGATTCTCCTGCCTCAGCCTCCCCAGTAGCTGGGATTACAGGCGCCCACCACCACGCTTG TCAAGTGATTCTCCTGCCTCAGCCTCCCCAGTGGCTGGGATTACAGGCGCCCACCACCACGCTTG T C TLK1 Ensembl:ENSG00000198586 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1201314025 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_377482,RMVar_hsa_circ_309751,RMVar_hsa_circ_204585,RMVar_hsa_circ_127448,RMVar_hsa_circ_204586,RMVar_hsa_circ_367869,RMVar_hsa_circ_89870,RMVar_hsa_circ_65337,RMVar_hsa_circ_27865,RMVar_hsa_circ_127131,RMVar_hsa_circ_204594,RMVar_hsa_circ_354329,RMVar_hsa_circ_312978,RMVar_hsa_circ_204598,RMVar_hsa_circ_343569,RMVar_hsa_circ_322077,RMVar_hsa_circ_359387,RMVar_hsa_circ_54203,RMVar_hsa_circ_320157,RMVar_hsa_circ_364027,RMVar_hsa_circ_361433,RMVar_hsa_circ_204602,RMVar_hsa_circ_108894,RMVar_hsa_circ_352992 40286 RMVar_ID_40286 Human_SNP_ID_101841676 A-to-I Human chr2 - 171074462 171074462 171074462 CAGCTTGCCTGGTTAGTTTTTGTATTTTCAGTAGAGACAAGGTTTCACCACATTGGCCAGGCTGA CAGCTTGCCTGGTTAGTTTTTGTATTTTCAGTGGAGACAAGGTTTCACCACATTGGCCAGGCTGA T C TLK1 Ensembl:ENSG00000198586 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1244513232 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_377482,RMVar_hsa_circ_309751,RMVar_hsa_circ_204585,RMVar_hsa_circ_127448,RMVar_hsa_circ_204586,RMVar_hsa_circ_367869,RMVar_hsa_circ_89870,RMVar_hsa_circ_65337,RMVar_hsa_circ_27865,RMVar_hsa_circ_127131,RMVar_hsa_circ_204594,RMVar_hsa_circ_354329,RMVar_hsa_circ_312978,RMVar_hsa_circ_204598,RMVar_hsa_circ_343569,RMVar_hsa_circ_322077,RMVar_hsa_circ_359387,RMVar_hsa_circ_54203,RMVar_hsa_circ_320157,RMVar_hsa_circ_364027,RMVar_hsa_circ_361433,RMVar_hsa_circ_204602,RMVar_hsa_circ_108894,RMVar_hsa_circ_352992 40287 RMVar_ID_40287 Human_SNP_ID_101841678 A-to-I Human chr2 - 171074480 171074480 171074480 GGGATTGTAGGCACCCACCAGCTTGCCTGGTTAGTTTTTGTATTTTCAGTAGAGACAAGGTTTCA GGGATTGTAGGCACCCACCAGCTTGCCTGGTTGGTTTTTGTATTTTCAGTAGAGACAAGGTTTCA T C TLK1 Ensembl:ENSG00000198586 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs770393216 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_377482,RMVar_hsa_circ_309751,RMVar_hsa_circ_204585,RMVar_hsa_circ_127448,RMVar_hsa_circ_204586,RMVar_hsa_circ_367869,RMVar_hsa_circ_89870,RMVar_hsa_circ_65337,RMVar_hsa_circ_27865,RMVar_hsa_circ_127131,RMVar_hsa_circ_204594,RMVar_hsa_circ_354329,RMVar_hsa_circ_312978,RMVar_hsa_circ_204598,RMVar_hsa_circ_343569,RMVar_hsa_circ_322077,RMVar_hsa_circ_359387,RMVar_hsa_circ_54203,RMVar_hsa_circ_320157,RMVar_hsa_circ_364027,RMVar_hsa_circ_361433,RMVar_hsa_circ_204602,RMVar_hsa_circ_108894,RMVar_hsa_circ_352992 40288 RMVar_ID_40288 Human_SNP_ID_101841713 A-to-I Human chr2 - 171074588 171074588 171074588 GAGTCTCGCTCTGTCACGCAGGTTGGAGTGCAATGGCACGATCTCTGCTCCCTGCAACCACTGCC GAGTCTCGCTCTGTCACGCAGGTTGGAGTGCAGTGGCACGATCTCTGCTCCCTGCAACCACTGCC T C TLK1 Ensembl:ENSG00000198586 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs898365621 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_377482,RMVar_hsa_circ_309751,RMVar_hsa_circ_204585,RMVar_hsa_circ_127448,RMVar_hsa_circ_204586,RMVar_hsa_circ_367869,RMVar_hsa_circ_89870,RMVar_hsa_circ_65337,RMVar_hsa_circ_27865,RMVar_hsa_circ_127131,RMVar_hsa_circ_204594,RMVar_hsa_circ_354329,RMVar_hsa_circ_312978,RMVar_hsa_circ_204598,RMVar_hsa_circ_343569,RMVar_hsa_circ_322077,RMVar_hsa_circ_359387,RMVar_hsa_circ_54203,RMVar_hsa_circ_320157,RMVar_hsa_circ_364027,RMVar_hsa_circ_361433,RMVar_hsa_circ_204602,RMVar_hsa_circ_108894,RMVar_hsa_circ_352992 40289 RMVar_ID_40289 Human_SNP_ID_101849150 A-to-I Human chr2 - 171103945 171103945 171103945 CTAGTTCATTGTTGGTGTATAGAAATGCTACTAATTTCTGTGTGTTGATTTTGTATTCTGCACCT CTAGTTCATTGTTGGTGTATAGAAATGCTACTTATTTCTGTGTGTTGATTTTGTATTCTGCACCT T A TLK1 Ensembl:ENSG00000198586 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs189520429 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_309751,RMVar_hsa_circ_204585,RMVar_hsa_circ_89870,RMVar_hsa_circ_127131,RMVar_hsa_circ_204594,RMVar_hsa_circ_354329,RMVar_hsa_circ_204598,RMVar_hsa_circ_343569,RMVar_hsa_circ_359387,RMVar_hsa_circ_364027,RMVar_hsa_circ_352992,RMVar_hsa_circ_204606,RMVar_hsa_circ_312373,RMVar_hsa_circ_204604,RMVar_hsa_circ_125471,RMVar_hsa_circ_285158,RMVar_hsa_circ_204605 40290 RMVar_ID_40290 Human_SNP_ID_101849151 A-to-I Human chr2 - 171103945 171103945 171103945 CTAGTTCATTGTTGGTGTATAGAAATGCTACTAATTTCTGTGTGTTGATTTTGTATTCTGCACCT CTAGTTCATTGTTGGTGTATAGAAATGCTACTGATTTCTGTGTGTTGATTTTGTATTCTGCACCT T C TLK1 Ensembl:ENSG00000198586 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs189520429 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_309751,RMVar_hsa_circ_204585,RMVar_hsa_circ_89870,RMVar_hsa_circ_127131,RMVar_hsa_circ_204594,RMVar_hsa_circ_354329,RMVar_hsa_circ_204598,RMVar_hsa_circ_343569,RMVar_hsa_circ_359387,RMVar_hsa_circ_364027,RMVar_hsa_circ_352992,RMVar_hsa_circ_204606,RMVar_hsa_circ_312373,RMVar_hsa_circ_204604,RMVar_hsa_circ_125471,RMVar_hsa_circ_285158,RMVar_hsa_circ_204605 40291 RMVar_ID_40291 Human_SNP_ID_101850949 A-to-I Human chr2 - 171111463 171111463 171111463 CCTCTATCTCAGCCTCCCAAGTAGCTGGGACTATAGGCGCTTGCACCATGACATTCGGCTAGTTT CCTCTATCTCAGCCTCCCAAGTAGCTGGGACTGTAGGCGCTTGCACCATGACATTCGGCTAGTTT T C TLK1 Ensembl:ENSG00000198586 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs751147215 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13675774 RMVar_hsa_circ_309751,RMVar_hsa_circ_204585,RMVar_hsa_circ_89870,RMVar_hsa_circ_127131,RMVar_hsa_circ_204594,RMVar_hsa_circ_354329,RMVar_hsa_circ_204598,RMVar_hsa_circ_343569,RMVar_hsa_circ_359387,RMVar_hsa_circ_364027,RMVar_hsa_circ_352992,RMVar_hsa_circ_204606,RMVar_hsa_circ_312373,RMVar_hsa_circ_204604,RMVar_hsa_circ_125471,RMVar_hsa_circ_285158,RMVar_hsa_circ_204605 40292 RMVar_ID_40292 Human_SNP_ID_101901727 A-to-I Human chr2 - 171322023 171322023 171322023 GGGAGGCAGAGGTTGCAGTGAGCCGAGATGACACCACTGCCCTCCAGCCTGGGTGACAGTTGTTA GGGAGGCAGAGGTTGCAGTGAGCCGAGATGACGCCACTGCCCTCCAGCCTGGGTGACAGTTGTTA T C METTL8 Ensembl:ENSG00000123600 Protein coding 3'UTR GSE47997;GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,29129909,31158229,31158229 RNA-Seq:(High) rs951470399 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25481419 40293 RMVar_ID_40293 Human_SNP_ID_101901736 A-to-I Human chr2 - 171322048 171322048 171322048 TGAGGCAGGAGAATCACTTGAACCCGGGAGGCAGAGGTTGCAGTGAGCCGAGATGACACCACTGC TGAGGCAGGAGAATCACTTGAACCCGGGAGGCGGAGGTTGCAGTGAGCCGAGATGACACCACTGC T C METTL8 Ensembl:ENSG00000123600 Protein coding 3'UTR GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line - 24183664,31158229 RNA-Seq:(High) rs1192936334 Functional Loss SNV dbSNP153 33..33 33 - - - 40294 RMVar_ID_40294 Human_SNP_ID_101901743 A-to-I Human chr2 - 171322100 171322082 171322100 AAATTAGCCAGGCGTGGTGGTGGGCACCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAA AAATTAGCCAGGCGTGGTGGTGGGCACCTGTA__________________GCTGAGGCAGGAGAA CCTCCCGAGTAGCTGGGAT C METTL8 Ensembl:ENSG00000123600 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1269108330 Functional Loss DEL dbSNP153 33..50 33 - - - 40295 RMVar_ID_40295 Human_SNP_ID_101901789 A-to-I Human chr2 - 171322243 171322243 171322243 TTATCCCCTCGAGGGCCGGGCGCAGTCGCTCAAGCCCGTAATCCCAGCACTTTGGGAGGCCGAGG TTATCCCCTCGAGGGCCGGGCGCAGTCGCTCAGGCCCGTAATCCCAGCACTTTGGGAGGCCGAGG T C METTL8 Ensembl:ENSG00000123600 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1201933538 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17570525 40296 RMVar_ID_40296 Human_SNP_ID_101901791 A-to-I Human chr2 - 171322252 171322252 171322252 AAAATGTATTTATCCCCTCGAGGGCCGGGCGCAGTCGCTCAAGCCCGTAATCCCAGCACTTTGGG AAAATGTATTTATCCCCTCGAGGGCCGGGCGCCGTCGCTCAAGCCCGTAATCCCAGCACTTTGGG T G METTL8 Ensembl:ENSG00000123600 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1040534290 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17570525 40297 RMVar_ID_40297 Human_SNP_ID_101901850 A-to-I Human chr2 - 171322493 171322493 171322493 TGACCTTGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCGC TGACCTTGTGATCCGCCCGCCTCGGCCTCCCACAGTGCTGGGATTACAGGTGTGAGCCACCGCGC T G METTL8 Ensembl:ENSG00000123600 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1359469298 Functional Loss SNV dbSNP153 33..33 33 - - - 40298 RMVar_ID_40298 Human_SNP_ID_101902108 A-to-I Human chr2 - 171323358 171323358 171323358 ATGGTGGCACACACCTGTGGTCCCAGCTACTCAGGAGACTGAGGTGGGAGGATCGCTTGAGCCTC ATGGTGGCACACACCTGTGGTCCCAGCTACTCGGGAGACTGAGGTGGGAGGATCGCTTGAGCCTC T C METTL8 Ensembl:ENSG00000123600 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs112273576 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25481425 40299 RMVar_ID_40299 Human_SNP_ID_101902144 A-to-I Human chr2 - 171323522 171323522 171323522 TCTTAGATATACAAGTTGTTAGGCCAGGTGCAATGGCTCGCACCTGTAATCCCAGCACTTTGGGG TCTTAGATATACAAGTTGTTAGGCCAGGTGCAGTGGCTCGCACCTGTAATCCCAGCACTTTGGGG T C METTL8 Ensembl:ENSG00000123600 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1015352322 Functional Loss SNV dbSNP153 33..33 33 - - - 40300 RMVar_ID_40300 Human_SNP_ID_101904948 A-to-I Human chr2 - 171335603 171335603 171335603 CTGGCCAACATGGTGAAACCCTGTCTCTACTAAAAATACAAAAATTAGCTGAGTGTGGTGGTGCA CTGGCCAACATGGTGAAACCCTGTCTCTACTAGAAATACAAAAATTAGCTGAGTGTGGTGGTGCA T C METTL8 Ensembl:ENSG00000123600 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1052100774 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_204613,RMVar_hsa_circ_350,RMVar_hsa_circ_33349,RMVar_hsa_circ_339185,RMVar_hsa_circ_204616,RMVar_hsa_circ_308569 40301 RMVar_ID_40301 Human_SNP_ID_101933103 A-to-I Human chr2 + 171454776 171454776 171454776 AAAATTAGCCACGGGTGGTAGTGCACACCTGTAGTCCCAGCTACTCGGGAGGCTGAGGTGGGAGA AAAATTAGCCACGGGTGGTAGTGCACACCTGTGGTCCCAGCTACTCGGGAGGCTGAGGTGGGAGA A G DCAF17 Ensembl:ENSG00000115827 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1455438610 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69,RMVar_hsa_circ_109374,RMVar_hsa_circ_204621,RMVar_hsa_circ_366622,RMVar_hsa_circ_347716,RMVar_hsa_circ_301064,RMVar_hsa_circ_51600,RMVar_hsa_circ_204623,RMVar_hsa_circ_37341,RMVar_hsa_circ_204624,RMVar_hsa_circ_284687,RMVar_hsa_circ_109317,RMVar_hsa_circ_204636,RMVar_hsa_circ_204631,RMVar_hsa_circ_279915,RMVar_hsa_circ_204625,RMVar_hsa_circ_290654,RMVar_hsa_circ_292062,RMVar_hsa_circ_283513,RMVar_hsa_circ_123330,RMVar_hsa_circ_270511,RMVar_hsa_circ_204633,RMVar_hsa_circ_204634,RMVar_hsa_circ_204632,RMVar_hsa_circ_204629,RMVar_hsa_circ_204630,RMVar_hsa_circ_204628,RMVar_hsa_circ_295236,RMVar_hsa_circ_322250,RMVar_hsa_circ_328684,RMVar_hsa_circ_50099,RMVar_hsa_circ_325712,RMVar_hsa_circ_306313,RMVar_hsa_circ_204638,RMVar_hsa_circ_204639,RMVar_hsa_circ_204637,RMVar_hsa_circ_204635 40302 RMVar_ID_40302 Human_SNP_ID_101937316 A-to-I Human chr2 + 171472359 171472359 171472359 ACACCACCATGCCCACTAATTTTTGTATTTTTAGTAGAAACAGGGTTTCATCTTGTTGGCCACGC ACACCACCATGCCCACTAATTTTTGTATTTTTGGTAGAAACAGGGTTTCATCTTGTTGGCCACGC A G DCAF17 Ensembl:ENSG00000115827 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1233967811 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109374,RMVar_hsa_circ_204621,RMVar_hsa_circ_51600,RMVar_hsa_circ_37341,RMVar_hsa_circ_109317,RMVar_hsa_circ_204636,RMVar_hsa_circ_204625,RMVar_hsa_circ_290654,RMVar_hsa_circ_292062,RMVar_hsa_circ_123330,RMVar_hsa_circ_204633,RMVar_hsa_circ_204634,RMVar_hsa_circ_204632,RMVar_hsa_circ_322250,RMVar_hsa_circ_328684,RMVar_hsa_circ_50099,RMVar_hsa_circ_91225,RMVar_hsa_circ_47963,RMVar_hsa_circ_204635,RMVar_hsa_circ_375501,RMVar_hsa_circ_204641,RMVar_hsa_circ_332873,RMVar_hsa_circ_204642,RMVar_hsa_circ_309043,RMVar_hsa_circ_204645 40303 RMVar_ID_40303 Human_SNP_ID_101937343 A-to-I Human chr2 + 171472447 171472447 171472447 GTGATCCACCTGCCTCGGCCTCCCAAAGTGCTAGGATTACAGGCGTAAGCCACTGCCCCCGGCCG GTGATCCACCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTAAGCCACTGCCCCCGGCCG A G DCAF17 Ensembl:ENSG00000115827 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1351629918 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109374,RMVar_hsa_circ_204621,RMVar_hsa_circ_51600,RMVar_hsa_circ_37341,RMVar_hsa_circ_109317,RMVar_hsa_circ_204636,RMVar_hsa_circ_204625,RMVar_hsa_circ_290654,RMVar_hsa_circ_292062,RMVar_hsa_circ_123330,RMVar_hsa_circ_204633,RMVar_hsa_circ_204634,RMVar_hsa_circ_204632,RMVar_hsa_circ_322250,RMVar_hsa_circ_328684,RMVar_hsa_circ_50099,RMVar_hsa_circ_91225,RMVar_hsa_circ_47963,RMVar_hsa_circ_204635,RMVar_hsa_circ_375501,RMVar_hsa_circ_204641,RMVar_hsa_circ_332873,RMVar_hsa_circ_204642,RMVar_hsa_circ_309043,RMVar_hsa_circ_204645 40304 RMVar_ID_40304 Human_SNP_ID_101950234 A-to-I Human chr2 + 171526656 171526656 171526656 GAAAGAAATGTTTCCCATGAAATAAGTATACTACTAGGAAATCAGAGAAACGAACCTTGAAAAGA GAAAGAAATGTTTCCCATGAAATAAGTATACTGCTAGGAAATCAGAGAAACGAACCTTGAAAAGA A G CYBRD1 Ensembl:ENSG00000071967 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1375161457 Functional Loss SNV dbSNP153 33..33 33 - - - 40305 RMVar_ID_40305 Human_SNP_ID_101951686 A-to-I Human chr2 + 171533183 171533183 171533183 GAGGTCAGGAGTTCGAGACGAGCCTGGCCAACATGGTGATACTCTATCTCTACTAAAAATACAAA GAGGTCAGGAGTTCGAGACGAGCCTGGCCAACCTGGTGATACTCTATCTCTACTAAAAATACAAA A C CYBRD1 Ensembl:ENSG00000071967 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs772892493 Functional Loss SNV dbSNP153 33..33 33 - - - 40306 RMVar_ID_40306 Human_SNP_ID_101951726 A-to-I Human chr2 + 171533349 171533349 171533349 AGATCCCGCCACTGCACTCTAGCCTGGGTGCAAAGAGAGAGACTCTGTCTCAGAAAACAAAAACA AGATCCCGCCACTGCACTCTAGCCTGGGTGCAGAGAGAGAGACTCTGTCTCAGAAAACAAAAACA A G CYBRD1 Ensembl:ENSG00000071967 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1321024808 Functional Loss SNV dbSNP153 33..33 33 - - - 40307 RMVar_ID_40307 Human_SNP_ID_101992476 A-to-I Human chr2 + 171697202 171697202 171697202 TTTTTGTTTTGTTTTTGTTTTTGTTTTTTTTTATAGAGATGGGGTCTCACTATGTTGCCAGGGCT TTTTTGTTTTGTTTTTGTTTTTGTTTTTTTTTGTAGAGATGGGGTCTCACTATGTTGCCAGGGCT A G DYNC1I2 Ensembl:ENSG00000077380 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs972045391 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21910,RMVar_hsa_circ_101825,RMVar_hsa_circ_363336,RMVar_hsa_circ_110358,RMVar_hsa_circ_30199,RMVar_hsa_circ_204649,RMVar_hsa_circ_204650 40308 RMVar_ID_40308 Human_SNP_ID_102004901 A-to-I Human chr2 + 171749374 171749374 171749374 ATATAGAAAAGTAGGCAATTCTTTACTTTTCTATATTCAGTTTCATAAATTAATACCCCATAATT ATATAGAAAAGTAGGCAATTCTTTACTTTTCTGTATTCAGTTTCATAAATTAATACCCCATAATT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs959627116 Functional Loss SNV dbSNP153 33..33 33 - - - 40309 RMVar_ID_40309 Human_SNP_ID_102009168 A-to-I Human chr2 + 171766532 171766532 171766532 ATGGTGGTAGGCTAATTTTGTATTAGGACTACAGGCGCCCGCCACCACACCCAGCTAATTTTTTG ATGGTGGTAGGCTAATTTTGTATTAGGACTACTGGCGCCCGCCACCACACCCAGCTAATTTTTTG A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1481371808 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13678361 40310 RMVar_ID_40310 Human_SNP_ID_102009206 A-to-I Human chr2 + 171766634 171766634 171766634 AGGATGGTCTCAATCTCCTGATCTCGTGACCCACCCGCCTCGGCCTCCCAAACTGCTGGGATTAC AGGATGGTCTCAATCTCCTGATCTCGTGACCCCCCCGCCTCGGCCTCCCAAACTGCTGGGATTAC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1044487230 Functional Loss SNV dbSNP153 33..33 33 - - - 40311 RMVar_ID_40311 Human_SNP_ID_102009566 A-to-I Human chr2 + 171767704 171767704 171767704 CAGGCTGGAATACAGTGTCACGATTTCAACTCACTGCAACCTCTATCTCTAGGGCTCAACTGATT CAGGCTGGAATACAGTGTCACGATTTCAACTCGCTGCAACCTCTATCTCTAGGGCTCAACTGATT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1028977421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22984699 40312 RMVar_ID_40312 Human_SNP_ID_102009570 A-to-I Human chr2 + 171767716 171767716 171767716 CAGTGTCACGATTTCAACTCACTGCAACCTCTATCTCTAGGGCTCAACTGATTCTCCCATCTCAG CAGTGTCACGATTTCAACTCACTGCAACCTCTGTCTCTAGGGCTCAACTGATTCTCCCATCTCAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs954348456 Functional Loss SNV dbSNP153 33..33 33 - - - 40313 RMVar_ID_40313 Human_SNP_ID_102009574 A-to-I Human chr2 + 171767742 171767742 171767742 ACCTCTATCTCTAGGGCTCAACTGATTCTCCCATCTCAGCCTCAGTAGCTGGGACCACAGGTACA ACCTCTATCTCTAGGGCTCAACTGATTCTCCCTTCTCAGCCTCAGTAGCTGGGACCACAGGTACA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs961540779 Functional Loss SNV dbSNP153 33..33 33 - - - 40314 RMVar_ID_40314 Human_SNP_ID_102015299 A-to-I Human chr2 - 171789794 171789794 171789794 TGCCTCCCGGGTTCAAGCGATTCTCCTGTGTCAGCCTCCCAAGTAGTTGGGACTACAGGCGTGTA TGCCTCCCGGGTTCAAGCGATTCTCCTGTGTCGGCCTCCCAAGTAGTTGGGACTACAGGCGTGTA T C SLC25A12 Ensembl:ENSG00000115840 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs572118348 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19557,RMVar_hsa_circ_366806,RMVar_hsa_circ_273129,RMVar_hsa_circ_204658,RMVar_hsa_circ_204659,RMVar_hsa_circ_204660,RMVar_hsa_circ_76318 40315 RMVar_ID_40315 Human_SNP_ID_102015443 A-to-I Human chr2 - 171790393 171790393 171790393 AGGAAGGAGCTGACTTGGAATAGAAGGAGAGAACCAGGTGTCCTTGGCTGCACCAACACTCTGAA AGGAAGGAGCTGACTTGGAATAGAAGGAGAGACCCAGGTGTCCTTGGCTGCACCAACACTCTGAA T G SLC25A12 Ensembl:ENSG00000115840 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1431920918 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19557,RMVar_hsa_circ_366806,RMVar_hsa_circ_273129,RMVar_hsa_circ_204658,RMVar_hsa_circ_204659,RMVar_hsa_circ_204660,RMVar_hsa_circ_76318 40316 RMVar_ID_40316 Human_SNP_ID_102015444 A-to-I Human chr2 - 171790396 171790396 171790396 GTTAGGAAGGAGCTGACTTGGAATAGAAGGAGAGAACCAGGTGTCCTTGGCTGCACCAACACTCT GTTAGGAAGGAGCTGACTTGGAATAGAAGGAGGGAACCAGGTGTCCTTGGCTGCACCAACACTCT T C SLC25A12 Ensembl:ENSG00000115840 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs907768688 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19557,RMVar_hsa_circ_366806,RMVar_hsa_circ_273129,RMVar_hsa_circ_204658,RMVar_hsa_circ_204659,RMVar_hsa_circ_204660,RMVar_hsa_circ_76318 40317 RMVar_ID_40317 Human_SNP_ID_102021764 A-to-I Human chr2 - 171818615 171818615 171818615 GGCATGTACTACCATGCCTGGCTAACTTTTGTATTTGTTGTAGAGATGGAGTTTTACCATGTTGC GGCATGTACTACCATGCCTGGCTAACTTTTGTGTTTGTTGTAGAGATGGAGTTTTACCATGTTGC T C SLC25A12 Ensembl:ENSG00000115840 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1209346144 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16224,RMVar_hsa_circ_38082,RMVar_hsa_circ_204660,RMVar_hsa_circ_76318,RMVar_hsa_circ_324860,RMVar_hsa_circ_289340,RMVar_hsa_circ_118659,RMVar_hsa_circ_204661,RMVar_hsa_circ_35892,RMVar_hsa_circ_119784,RMVar_hsa_circ_34960,RMVar_hsa_circ_5817,RMVar_hsa_circ_67886,RMVar_hsa_circ_204663,RMVar_hsa_circ_204664,RMVar_hsa_circ_12578 40318 RMVar_ID_40318 Human_SNP_ID_102022827 A-to-I Human chr2 - 171822532 171822532 171822532 AAACATACAAAAAATTAGCCAGGCATGGTAGTATGCACCTGTAGTCTCAGCTATTTGGGAGACAG AAACATACAAAAAATTAGCCAGGCATGGTAGTGTGCACCTGTAGTCTCAGCTATTTGGGAGACAG T C SLC25A12 Ensembl:ENSG00000115840 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1234664266 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16224,RMVar_hsa_circ_38082,RMVar_hsa_circ_204660,RMVar_hsa_circ_76318,RMVar_hsa_circ_324860,RMVar_hsa_circ_289340,RMVar_hsa_circ_118659,RMVar_hsa_circ_204661,RMVar_hsa_circ_35892,RMVar_hsa_circ_119784,RMVar_hsa_circ_34960,RMVar_hsa_circ_5817,RMVar_hsa_circ_67886,RMVar_hsa_circ_204663,RMVar_hsa_circ_204664,RMVar_hsa_circ_12578 40319 RMVar_ID_40319 Human_SNP_ID_102029782 A-to-I Human chr2 - 171853581 171853581 171853581 TGCCTCCTGGGTTCAAGCGATTCTTCTGCTTCAGCTTCCCGAGTACCTGGGATTACAGGCACCTG TGCCTCCTGGGTTCAAGCGATTCTTCTGCTTCCGCTTCCCGAGTACCTGGGATTACAGGCACCTG T G SLC25A12 Ensembl:ENSG00000115840 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1471656881 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_289340,RMVar_hsa_circ_118659,RMVar_hsa_circ_204661,RMVar_hsa_circ_22181,RMVar_hsa_circ_5817,RMVar_hsa_circ_67886,RMVar_hsa_circ_204664,RMVar_hsa_circ_286524,RMVar_hsa_circ_204665,RMVar_hsa_circ_286485,RMVar_hsa_circ_23434,RMVar_hsa_circ_288247 40320 RMVar_ID_40320 Human_SNP_ID_102031384 A-to-I Human chr2 - 171860899 171860899 171860899 TTTGGTATTTTTTGTAGAGATAGGGTCTTTCTATGTTGCTTAGGCTGGTCTTGAACTTTTGGGCT TTTGGTATTTTTTGTAGAGATAGGGTCTTTCTGTGTTGCTTAGGCTGGTCTTGAACTTTTGGGCT T C SLC25A12 Ensembl:ENSG00000115840 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs148263065 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118659,RMVar_hsa_circ_204661,RMVar_hsa_circ_22181,RMVar_hsa_circ_267078,RMVar_hsa_circ_362273 40321 RMVar_ID_40321 Human_SNP_ID_102031870 A-to-I Human chr2 - 171863028 171863028 171863028 AGTTGTGATGGTGTGTGCCTATAGCCTTAGCTACTTGGGAGAGTGAGGCAGGAGGATTGTTTGAG AGTTGTGATGGTGTGTGCCTATAGCCTTAGCTGCTTGGGAGAGTGAGGCAGGAGGATTGTTTGAG T C SLC25A12 Ensembl:ENSG00000115840 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs535793551 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118659,RMVar_hsa_circ_204661,RMVar_hsa_circ_22181,RMVar_hsa_circ_267078,RMVar_hsa_circ_362273 40322 RMVar_ID_40322 Human_SNP_ID_102049641 A-to-I Human chr2 + 171930668 171930668 171930668 AGAGTGGCTCACTCCATTGCCAAGGCTGGAGTAGAGTGGCGTGATTGTGGCTCACTATAGCCTTG AGAGTGGCTCACTCCATTGCCAAGGCTGGAGTGGAGTGGCGTGATTGTGGCTCACTATAGCCTTG A G HAT1 Ensembl:ENSG00000128708 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1236593164 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13679268 RMVar_hsa_circ_284978,RMVar_hsa_circ_307482,RMVar_hsa_circ_333082,RMVar_hsa_circ_293951,RMVar_hsa_circ_281411,RMVar_hsa_circ_54208,RMVar_hsa_circ_61662 40323 RMVar_ID_40323 Human_SNP_ID_102059392 A-to-I Human chr2 + 171974072 171974072 171974072 ATGGTGGCAAGCACCCGTGGGCCCAGCTACTCAGGAGGCTGAGGTGGGAGGATCACTGGAGCCCA ATGGTGGCAAGCACCCGTGGGCCCAGCTACTCGGGAGGCTGAGGTGGGAGGATCACTGGAGCCCA A G HAT1 Ensembl:ENSG00000128708 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984479108 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1132,RMVar_hsa_circ_307482,RMVar_hsa_circ_281411 40324 RMVar_ID_40324 Human_SNP_ID_102069562 A-to-I Human chr2 + 172016075 172016075 172016075 GGTCAGGAGTTCGAGATCGGCCTGGCTAATATAGTGAAACTCCGTCTCTATCAAAAAAAAAAAAA GGTCAGGAGTTCGAGATCGGCCTGGCTAATATGGTGAAACTCCGTCTCTATCAAAAAAAAAAAAA A G METAP1D Ensembl:ENSG00000172878 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs539018993 Functional Loss SNV dbSNP153 33..33 33 - - - 40325 RMVar_ID_40325 Human_SNP_ID_102083481 A-to-I Human chr2 + 172068613 172068613 172068613 TCAGCTCACTGCAAACTCCGCCTTAAGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCCAGTAAC TCAGCTCACTGCAAACTCCGCCTTAAGGGTTCGAGTGATTCTCCTGCCTCAGCCTCCCCAGTAAC A G METAP1D Ensembl:ENSG00000172878 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs866978589 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50040,RMVar_hsa_circ_26412,RMVar_hsa_circ_204671 40326 RMVar_ID_40326 Human_SNP_ID_102185892 A-to-I Human chr2 - 172493001 172493001 172493001 CAGGAGGTGAGACAGGAGGATTGCTTGAGCCCAGGCATTCAAGGCTGCAGTGAGCTGTGTTTGCG CAGGAGGTGAGACAGGAGGATTGCTTGAGCCCGGGCATTCAAGGCTGCAGTGAGCTGTGTTTGCG T C AC078883.1 Ensembl:ENSG00000225205 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1485497288 Functional Loss SNV dbSNP153 33..33 33 - - - 40327 RMVar_ID_40327 Human_SNP_ID_102205021 A-to-I Human chr2 + 172566446 172566446 172566446 GCGTGGTGACCCATGCCTACGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAA GCGTGGTGACCCATGCCTACGTAGTCCCAGCTGCTTGGGAGGCTGAGGCAGGAGAATCGCTTGAA A G PDK1 Ensembl:ENSG00000152256 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1213791509 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44787,RMVar_hsa_circ_204679,RMVar_hsa_circ_95050,RMVar_hsa_circ_204678,RMVar_hsa_circ_116403,RMVar_hsa_circ_342186,RMVar_hsa_circ_294869,RMVar_hsa_circ_273407,RMVar_hsa_circ_57689,RMVar_hsa_circ_78464,RMVar_hsa_circ_204681,RMVar_hsa_circ_204682,RMVar_hsa_circ_204680,RMVar_hsa_circ_72567,RMVar_hsa_circ_359940,RMVar_hsa_circ_325459,RMVar_hsa_circ_86035,RMVar_hsa_circ_204688,RMVar_hsa_circ_116067,RMVar_hsa_circ_204692,RMVar_hsa_circ_305252,RMVar_hsa_circ_372128,RMVar_hsa_circ_204689,RMVar_hsa_circ_350991,RMVar_hsa_circ_204691,RMVar_hsa_circ_127057,RMVar_hsa_circ_294501,RMVar_hsa_circ_204693,RMVar_hsa_circ_204694 40328 RMVar_ID_40328 Human_SNP_ID_102466304 A-to-I Human chr2 - 173671524 173671524 173671524 GTATACATGATTCAGAAGGGATATGTAAAACAATCATTTAAAGGCAGGACTTATGGTAAGCATAA GTATACATGATTCAGAAGGGATATGTAAAACAGTCATTTAAAGGCAGGACTTATGGTAAGCATAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041234131 Functional Loss SNV dbSNP153 33..33 33 - - - 40329 RMVar_ID_40329 Human_SNP_ID_102523491 A-to-I Human chr2 - 173910102 173910102 173910102 CTGTGGAAGCTGCGCGAGATGATACTTTGATTACTGCAGGAGGAACAACGCTTATCCTTGCAAAT CTGTGGAAGCTGCGCGAGATGATACTTTGATTGCTGCAGGAGGAACAACGCTTATCCTTGCAAAT T C SP3 Ensembl:ENSG00000172845 Protein coding intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1374284157 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1580018,Human_RBP_ID_1902826,Human_RBP_ID_3604260,Human_RBP_ID_6851708,Human_RBP_ID_8505085,Human_RBP_ID_13682439,Human_RBP_ID_17274165,Human_RBP_ID_18311798,Human_RBP_ID_18749678,Human_RBP_ID_22073024,Human_RBP_ID_27475912,Human_RBP_ID_27688950 40330 RMVar_ID_40330 Human_SNP_ID_102526550 A-to-I Human chr2 - 173922020 173922020 173922020 TGACTCAGTTCTGCAGGCTGTACCGGAAGCATAGTGCTGGCATCTGGGTCTGGGAAGGCCTCAAG TGACTCAGTTCTGCAGGCTGTACCGGAAGCATGGTGCTGGCATCTGGGTCTGGGAAGGCCTCAAG T C SP3 Ensembl:ENSG00000172845 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs573807235 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25580,RMVar_hsa_circ_350158,RMVar_hsa_circ_204735,RMVar_hsa_circ_204736,RMVar_hsa_circ_271251 40331 RMVar_ID_40331 Human_SNP_ID_102529904 A-to-I Human chr2 - 173933976 173933975 173933976 CCTCCCACCTCTGCCTCCAAGTAACTGGGACTACAGATGTACACCACCACATCCAACTCTTATTT CCTCCCACCTCTGCCTCCAAGTAACTGGGACT_CAGATGTACACCACCACATCCAACTCTTATTT GT G SP3 Ensembl:ENSG00000172845 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1392871043 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_25580,RMVar_hsa_circ_350158,RMVar_hsa_circ_204735,RMVar_hsa_circ_204736,RMVar_hsa_circ_271251 40332 RMVar_ID_40332 Human_SNP_ID_102532466 A-to-I Human chr2 - 173943530 173943530 173943530 GCCCAGGAGTTCGAGACCAGCCTGGGCAACATAGTGAGACCCCCATCTCATAAAAAAGAAAATTA GCCCAGGAGTTCGAGACCAGCCTGGGCAACATGGTGAGACCCCCATCTCATAAAAAAGAAAATTA T C SP3 Ensembl:ENSG00000172845 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1023929534 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25580,RMVar_hsa_circ_350158,RMVar_hsa_circ_204735,RMVar_hsa_circ_204736,RMVar_hsa_circ_271251 40333 RMVar_ID_40333 Human_SNP_ID_102540510 A-to-I Human chr2 + 173968471 173968471 173968471 CAGCATGCCTGGCTAAGTTTTGTATTTTTAGTAAAGACAGGGTTTCACCATGTTGGCCAGGCTGG CAGCATGCCTGGCTAAGTTTTGTATTTTTAGTGAAGACAGGGTTTCACCATGTTGGCCAGGCTGG A G AC016737.1 Ensembl:ENSG00000271151 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs990080796 Functional Loss SNV dbSNP153 33..33 33 - - - 40334 RMVar_ID_40334 Human_SNP_ID_102541942 A-to-I Human chr2 + 173974727 173974727 173974727 TTGAGACAAGGTCTCACTGTGTCTCCCAGGCTAGAGTGCAGTGGTGCCATCTTGGCTCACTGCAA TTGAGACAAGGTCTCACTGTGTCTCCCAGGCTGGAGTGCAGTGGTGCCATCTTGGCTCACTGCAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1373925696 Functional Loss SNV dbSNP153 33..33 33 - - - 40335 RMVar_ID_40335 Human_SNP_ID_102573548 A-to-I Human chr2 - 174113078 174113078 174113078 AAATTAGCTGGGCTTGGTGGCGGGCACCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAA AAATTAGCTGGGCTTGGTGGCGGGCACCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAA T C OLA1 Ensembl:ENSG00000138430 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs913311946 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_348394 40336 RMVar_ID_40336 Human_SNP_ID_102581403 A-to-I Human chr2 - 174148376 174148376 174148376 TGTTTTGTTTTGTTTATTTGAGATGTAGTCTCACTCTTGTCGCTCCGGCTGGAGTACAGTGGCAC TGTTTTGTTTTGTTTATTTGAGATGTAGTCTCGCTCTTGTCGCTCCGGCTGGAGTACAGTGGCAC T C OLA1 Ensembl:ENSG00000138430 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256385011 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63126,RMVar_hsa_circ_356902 40337 RMVar_ID_40337 Human_SNP_ID_102586512 A-to-I Human chr2 - 174170782 174170782 174170782 CTCCCACTTCAGCCTCTTGAGTAAGTGGGACTACAGGCTCATGTCACCATGCCTGGCTAATTTTT CTCCCACTTCAGCCTCTTGAGTAAGTGGGACTGCAGGCTCATGTCACCATGCCTGGCTAATTTTT T C OLA1 Ensembl:ENSG00000138430 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1030588015 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13685268 RMVar_hsa_circ_63126,RMVar_hsa_circ_356902 40338 RMVar_ID_40338 Human_SNP_ID_102596911 A-to-I Human chr2 - 174219584 174219584 174219584 TCTCTACCAAAAATACAAAAAATTAGCTGGGTATGGTGGCATGTGCCTGTGGTCTCAGCTACTCG TCTCTACCAAAAATACAAAAAATTAGCTGGGTGTGGTGGCATGTGCCTGTGGTCTCAGCTACTCG T C OLA1 Ensembl:ENSG00000138430 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1019902450 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63126,RMVar_hsa_circ_356902 40339 RMVar_ID_40339 Human_SNP_ID_102596932 A-to-I Human chr2 - 174219689 174219689 174219689 GGCTGAGCACGGTGGCTCATGCCTGTAACCCCAGCATTTTGGGAGACTGGGGCAGGCAGATTGCT GGCTGAGCACGGTGGCTCATGCCTGTAACCCCGGCATTTTGGGAGACTGGGGCAGGCAGATTGCT T C OLA1 Ensembl:ENSG00000138430 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs914162938 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17570056 RMVar_hsa_circ_63126,RMVar_hsa_circ_356902 40340 RMVar_ID_40340 Human_SNP_ID_102596970 A-to-I Human chr2 - 174219873 174219873 174219873 CCCACCTCAGCCTCCCAAAGTGCTGAGATTACAGGTGTGAGCCACTGTGCCCAGCCTAAATATAA CCCACCTCAGCCTCCCAAAGTGCTGAGATTACGGGTGTGAGCCACTGTGCCCAGCCTAAATATAA T C OLA1 Ensembl:ENSG00000138430 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1283626004 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63126,RMVar_hsa_circ_356902 40341 RMVar_ID_40341 Human_SNP_ID_102597008 A-to-I Human chr2 - 174219984 174219981 174219984 GGGATTACAGAGGCACACCACCACACCAGGCTACTTTTTGTATTTTTAGTAGAGACGGGATTTCA GGGATTACAGAGGCACACCACCACACCAGGCT___TTTTGTATTTTTAGTAGAGACGGGATTTCA AAGT A OLA1 Ensembl:ENSG00000138430 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1395955870 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_63126,RMVar_hsa_circ_356902 40342 RMVar_ID_40342 Human_SNP_ID_102660678 A-to-I Human chr2 - 174484766 174484766 174484766 GCACGCATGACTAAGCTCAGCTAATTTTTTGTAGAGACTAAGGTTTTGCCATGTTGGCCAGGCTG GCACGCATGACTAAGCTCAGCTAATTTTTTGTGGAGACTAAGGTTTTGCCATGTTGGCCAGGCTG T C GPR155 Ensembl:ENSG00000163328 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs746678307 Functional Loss SNV dbSNP153 33..33 33 - - - 40343 RMVar_ID_40343 Human_SNP_ID_102664845 A-to-I Human chr2 + 174502111 174502111 174502111 TTTTAGATGGAGAAGGAAAAAATGGAACCATCAAACTGATGGAACCCCTTGATGAAGAAATCTCT TTTTAGATGGAGAAGGAAAAAATGGAACCATCGAACTGATGGAACCCCTTGATGAAGAAATCTCT A G AC010894.1 Ensembl:ENSG00000179997 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404654260 Functional Loss SNV dbSNP153 33..33 33 - - - 40344 RMVar_ID_40344 Human_SNP_ID_102664857 A-to-I Human chr2 + 174502150 174502150 174502150 TGGAACCCCTTGATGAAGAAATCTCTGGAATTATGGAAGTGGTTGGAAGAGTAACCGCTAAGGCC TGGAACCCCTTGATGAAGAAATCTCTGGAATTGTGGAAGTGGTTGGAAGAGTAACCGCTAAGGCC A G AC010894.1 Ensembl:ENSG00000179997 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1193704380 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17394152 40345 RMVar_ID_40345 Human_SNP_ID_102682573 A-to-I Human chr2 - 174577741 174577741 174577741 CTCATTTTTTGTAGAGATGGGAATCTCACCATATTGCTCAGACTGGTCCTGAACTCCTGAGCTCA CTCATTTTTTGTAGAGATGGGAATCTCACCATGTTGCTCAGACTGGTCCTGAACTCCTGAGCTCA T C WIPF1 Ensembl:ENSG00000115935 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1030629915 Functional Loss SNV dbSNP153 33..33 33 - - - 40346 RMVar_ID_40346 Human_SNP_ID_102703450 A-to-I Human chr2 - 174677054 174677054 174677054 GACTTCCCAGGCCCAAATGATCCTCCTACCTTAGCCTCCCAAGTAAGCTCGGATAACAGGTGTGC GACTTCCCAGGCCCAAATGATCCTCCTACCTTGGCCTCCCAAGTAAGCTCGGATAACAGGTGTGC T C WIPF1 Ensembl:ENSG00000115935 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1452446638 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_325730,Human_Splice_Rec_325731 40347 RMVar_ID_40347 Human_SNP_ID_102703454 A-to-I Human chr2 - 174677070 174677070 174677070 AGTTCGCTGCAGCCTCGACTTCCCAGGCCCAAATGATCCTCCTACCTTAGCCTCCCAAGTAAGCT AGTTCGCTGCAGCCTCGACTTCCCAGGCCCAAGTGATCCTCCTACCTTAGCCTCCCAAGTAAGCT T C WIPF1 Ensembl:ENSG00000115935 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs990544057 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_325730,Human_Splice_Rec_325731 40348 RMVar_ID_40348 Human_SNP_ID_102733942 A-to-I Human chr2 - 174802976 174802976 174802976 TAGAGCACAGTGATGCAATCCTGGCTCACTGCAACCTCCACCTCCTGGGTTCAAGTAATTCTCCT TAGAGCACAGTGATGCAATCCTGGCTCACTGCCACCTCCACCTCCTGGGTTCAAGTAATTCTCCT T G CHN1 Ensembl:ENSG00000128656 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1185232077 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47704,RMVar_hsa_circ_89558,RMVar_hsa_circ_204761 40349 RMVar_ID_40349 Human_SNP_ID_102736765 A-to-I Human chr2 - 174815265 174815265 174815265 CAGGCAATCCTCCCACCACAAGCCCGCTGAGTAGCTGGAACTACAGGCGCACACCACCACAACCA CAGGCAATCCTCCCACCACAAGCCCGCTGAGTGGCTGGAACTACAGGCGCACACCACCACAACCA T C CHN1 Ensembl:ENSG00000128656 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1335669065 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47704,RMVar_hsa_circ_16281,RMVar_hsa_circ_312846,RMVar_hsa_circ_326813,RMVar_hsa_circ_49602,RMVar_hsa_circ_204762 40350 RMVar_ID_40350 Human_SNP_ID_102737060 A-to-I Human chr2 - 174816416 174816416 174816416 CCATTCTCTAGGTAAACAGAGACCCTTCTGCTACACCTTCTCAGTGGATGCTGCAGCAGCAGAGT CCATTCTCTAGGTAAACAGAGACCCTTCTGCTGCACCTTCTCAGTGGATGCTGCAGCAGCAGAGT T C CHN1 Ensembl:ENSG00000128656 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1214383003 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47704,RMVar_hsa_circ_16281,RMVar_hsa_circ_312846,RMVar_hsa_circ_326813,RMVar_hsa_circ_49602,RMVar_hsa_circ_204762 40351 RMVar_ID_40351 Human_SNP_ID_102767350 A-to-I Human chr2 - 174946846 174946846 174946846 CGCTATGTTGCCAGGCTGGTCTCTTGAGCTCAAATGATCCTCCCACCTTGGCCTCCCAAAGTGCT CGCTATGTTGCCAGGCTGGTCTCTTGAGCTCAGATGATCCTCCCACCTTGGCCTCCCAAAGTGCT T C CHN1 Ensembl:ENSG00000128656 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1225677051 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13688381,Human_RBP_ID_25485289 RMVar_hsa_circ_16281,RMVar_hsa_circ_49602,RMVar_hsa_circ_40038,RMVar_hsa_circ_27577,RMVar_hsa_circ_36641,RMVar_hsa_circ_204770,RMVar_hsa_circ_277678,RMVar_hsa_circ_204776,RMVar_hsa_circ_204774,RMVar_hsa_circ_204775,RMVar_hsa_circ_204777 40352 RMVar_ID_40352 Human_SNP_ID_102797286 A-to-I Human chr2 - 175073679 175073674 175073679 GGTTGCCAGAAAAGCCTAAAATTACTACTTAGAAAATTTAAGACTGTTTACCCCCATTGTCTTGT GGTTGCCAGAAAAGCCTAAAATTACTACTTAG_____TTAAGACTGTTTACCCCCATTGTCTTGT AATTTT A ATF2 Ensembl:ENSG00000115966 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1385749663 Functional Loss DEL dbSNP153 33..37 33 - - - Human_RBP_ID_1020913,Human_RBP_ID_1903318,Human_RBP_ID_2603595,Human_RBP_ID_6853876,Human_RBP_ID_13689223,Human_RBP_ID_17389417,Human_RBP_ID_18311913,Human_RBP_ID_18749884,Human_RBP_ID_23838804,Human_RBP_ID_25485421,Human_RBP_ID_27689141 40353 RMVar_ID_40353 Human_SNP_ID_102800121 A-to-I Human chr2 - 175085313 175085313 175085313 CCAGGCTGGTCTTAAACTCCTGACCTCAAGTTATCTGCCCGCCTCAGTCTCCCAAAGTTCTGGGA CCAGGCTGGTCTTAAACTCCTGACCTCAAGTTTTCTGCCCGCCTCAGTCTCCCAAAGTTCTGGGA T A ATF2 Ensembl:ENSG00000115966 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs374910529 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10673,RMVar_hsa_circ_107905,RMVar_hsa_circ_204778,RMVar_hsa_circ_280005,RMVar_hsa_circ_314040,RMVar_hsa_circ_351599,RMVar_hsa_circ_325322,RMVar_hsa_circ_309051,RMVar_hsa_circ_277132,RMVar_hsa_circ_204782,RMVar_hsa_circ_204783,RMVar_hsa_circ_204784,RMVar_hsa_circ_204781 40354 RMVar_ID_40354 Human_SNP_ID_102800131 A-to-I Human chr2 - 175085352 175085352 175085352 TCTTATATTTTTAGTAGAGACAGGGTTTCACCACGTTGGCCAGGCTGGTCTTAAACTCCTGACCT TCTTATATTTTTAGTAGAGACAGGGTTTCACCGCGTTGGCCAGGCTGGTCTTAAACTCCTGACCT T C ATF2 Ensembl:ENSG00000115966 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1399016225 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10673,RMVar_hsa_circ_107905,RMVar_hsa_circ_204778,RMVar_hsa_circ_280005,RMVar_hsa_circ_314040,RMVar_hsa_circ_351599,RMVar_hsa_circ_325322,RMVar_hsa_circ_309051,RMVar_hsa_circ_277132,RMVar_hsa_circ_204782,RMVar_hsa_circ_204783,RMVar_hsa_circ_204784,RMVar_hsa_circ_204781 40355 RMVar_ID_40355 Human_SNP_ID_102800903 A-to-I Human chr2 - 175088588 175088588 175088588 GCCATTAAAGGTAACGGCAAAACATACTTTTAATGGCAAAAACTGTGATTCCGTTTGCACCAACC GCCATTAAAGGTAACGGCAAAACATACTTTTAGTGGCAAAAACTGTGATTCCGTTTGCACCAACC T C ATF2 Ensembl:ENSG00000115966 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1181636161 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13689452 RMVar_hsa_circ_10673,RMVar_hsa_circ_107905,RMVar_hsa_circ_204778,RMVar_hsa_circ_280005,RMVar_hsa_circ_314040,RMVar_hsa_circ_351599,RMVar_hsa_circ_325322,RMVar_hsa_circ_309051,RMVar_hsa_circ_277132,RMVar_hsa_circ_204782,RMVar_hsa_circ_204783,RMVar_hsa_circ_204784,RMVar_hsa_circ_204781 40356 RMVar_ID_40356 Human_SNP_ID_102818085 A-to-I Human chr2 - 175159243 175159243 175159243 AGGTTCTCAGCTCACTGAACCCTCCACCTCCCAGGCTCAAGCAGTTCTCATGCCTCAGCCTTTTG AGGTTCTCAGCTCACTGAACCCTCCACCTCCCTGGCTCAAGCAGTTCTCATGCCTCAGCCTTTTG T A ATF2 Ensembl:ENSG00000115966 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1473502785 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14001269 40357 RMVar_ID_40357 Human_SNP_ID_102818347 A-to-I Human chr2 - 175160298 175160298 175160298 TCACTGCTGCCTCAAACACCTGGGCTTCAGCAATCCTCCCACCTCAGCCTCCCGAGTAGCTGGGA TCACTGCTGCCTCAAACACCTGGGCTTCAGCAGTCCTCCCACCTCAGCCTCCCGAGTAGCTGGGA T C ATF2 Ensembl:ENSG00000115966 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1290189145 Functional Loss SNV dbSNP153 33..33 33 - - - 40358 RMVar_ID_40358 Human_SNP_ID_102819183 A-to-I Human chr2 - 175163687 175163687 175163687 AACCTGCCTCGGCCTCCCAAAGTGTTGGAATTACAGGCATGAGCCACCACCCAGCATCATTTTTC AACCTGCCTCGGCCTCCCAAAGTGTTGGAATTCCAGGCATGAGCCACCACCCAGCATCATTTTTC T G ATF2 Ensembl:ENSG00000115966 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1397308849 Functional Loss SNV dbSNP153 33..33 33 - - - 40359 RMVar_ID_40359 Human_SNP_ID_102995413 A-to-I Human chr2 - 175920949 175920949 175920949 TGAGGCAGAAGAATTGCTTGAATTCCAGAGGCAGAGGTTGCACTGAGCCAAGATCGTGCCGCCGC TGAGGCAGAAGAATTGCTTGAATTCCAGAGGCGGAGGTTGCACTGAGCCAAGATCGTGCCGCCGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs550624196 Functional Loss SNV dbSNP153 33..33 33 - - - 40360 RMVar_ID_40360 Human_SNP_ID_102996705 A-to-I Human chr2 - 175926454 175926454 175926454 TTGGCTCACAGTTCTGGAACCTGGGAAATCCAAAGGCATGATGCTAGCATCTGGTGAGGGCCTTT TTGGCTCACAGTTCTGGAACCTGGGAAATCCAGAGGCATGATGCTAGCATCTGGTGAGGGCCTTT T C LNPK Ensembl:ENSG00000144320 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,31158229,32596459 RNA-Seq:(High) rs1272961043 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_538629,Human_RBP_ID_6854538 Human_miRNA_ID_1698054 40361 RMVar_ID_40361 Human_SNP_ID_102996712 A-to-I Human chr2 - 175926492 175926492 175926492 ATACCACAGACTGGGTAACGTGATGAACAAAAATTTATTTGGCTCACAGTTCTGGAACCTGGGAA ATACCACAGACTGGGTAACGTGATGAACAAAAGTTTATTTGGCTCACAGTTCTGGAACCTGGGAA T C LNPK Ensembl:ENSG00000144320 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs998524630 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6854539,Human_RBP_ID_13691401 Human_miRNA_ID_183691 40362 RMVar_ID_40362 Human_SNP_ID_103001167 A-to-I Human chr2 - 175945027 175945027 175945027 GGGCCTGGTGGCAGGTGCCTGTATTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATTGCTGGAA GGGCCTGGTGGCAGGTGCCTGTATTCCCAGCTGCTTGGGAGGCTGAGGCAGGAGAATTGCTGGAA T C LNPK Ensembl:ENSG00000144320 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1298682733 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97582,RMVar_hsa_circ_67734,RMVar_hsa_circ_204803,RMVar_hsa_circ_329824,RMVar_hsa_circ_349472,RMVar_hsa_circ_124466,RMVar_hsa_circ_125585,RMVar_hsa_circ_107850,RMVar_hsa_circ_204804,RMVar_hsa_circ_204806,RMVar_hsa_circ_204807,RMVar_hsa_circ_204805 40363 RMVar_ID_40363 Human_SNP_ID_103067569 A-to-I Human chr2 - 176200949 176200949 176200949 AGAAGAAAGTGGAAGCAAAGAAAGAAGAATCCAAGGAGTCTGATGATGACATGGGCCTTGGTCTT AGAAGAAAGTGGAAGCAAAGAAAGAAGAATCCGAGGAGTCTGATGATGACATGGGCCTTGGTCTT T C AC016739.1 Ensembl:ENSG00000218175 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879049373 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_538881,Human_RBP_ID_5100089,Human_RBP_ID_17699967,Human_RBP_ID_18534128 40364 RMVar_ID_40364 Human_SNP_ID_103067622 A-to-I Human chr2 - 176201133 176201133 176201133 GCCCTCATTAAAGCAGCCGGTGTAAATGTTGAACCTTTTTGGCCTGGCTTGTTTGCAAAGGCCCT GCCCTCATTAAAGCAGCCGGTGTAAATGTTGAGCCTTTTTGGCCTGGCTTGTTTGCAAAGGCCCT T C AC016739.1 Ensembl:ENSG00000218175 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-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 40365 RMVar_ID_40365 Human_SNP_ID_103094864 A-to-I Human chr2 + 176312708 176312708 176312708 CAACATGGTGAAACCCCATCTCTACTAAATACAAAAAATTAGCCAGGGGTGGTGGCGCATGCCTG CAACATGGTGAAACCCCATCTCTACTAAATACGAAAAATTAGCCAGGGGTGGTGGCGCATGCCTG A G MTX2 Ensembl:ENSG00000128654 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs996626376 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10483,RMVar_hsa_circ_375798,RMVar_hsa_circ_378513,RMVar_hsa_circ_312191,RMVar_hsa_circ_304213,RMVar_hsa_circ_204819,RMVar_hsa_circ_204820,RMVar_hsa_circ_204821,RMVar_hsa_circ_204818 40366 RMVar_ID_40366 Human_SNP_ID_103095115 A-to-I Human chr2 + 176313479 176313479 176313479 CAGTGGTGTGATCTTGGCTCACTGCAACTTCCATCTCCCAGGCTCAAGTGATTGTCCTGCCTCAG CAGTGGTGTGATCTTGGCTCACTGCAACTTCCGTCTCCCAGGCTCAAGTGATTGTCCTGCCTCAG A G MTX2 Ensembl:ENSG00000128654 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs570071796 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10483,RMVar_hsa_circ_375798,RMVar_hsa_circ_378513,RMVar_hsa_circ_312191,RMVar_hsa_circ_304213,RMVar_hsa_circ_204819,RMVar_hsa_circ_204820,RMVar_hsa_circ_204821,RMVar_hsa_circ_204818 40367 RMVar_ID_40367 Human_SNP_ID_103095294 A-to-I Human chr2 + 176314202 176314201 176314203 CTCACGCCTCTAATCCCAGCACTTTGGAATGTAAGACGGGCAGATCACTTGAGGCCAGGAGTTCA CTCACGCCTCTAATCCCAGCACTTTGGAATGT__GACGGGCAGATCACTTGAGGCCAGGAGTTCA TAA T MTX2 Ensembl:ENSG00000128654 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1249368202 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_10483,RMVar_hsa_circ_375798,RMVar_hsa_circ_378513,RMVar_hsa_circ_312191,RMVar_hsa_circ_304213,RMVar_hsa_circ_204819,RMVar_hsa_circ_204820,RMVar_hsa_circ_204821,RMVar_hsa_circ_204818 40368 RMVar_ID_40368 Human_SNP_ID_103297016 A-to-I Human chr2 - 177179806 177179806 177179806 CAGATGCACCCCACCATGCCTGGCTAACTTTTATATTTTTTGTAGCAGTCTCACTGTGTTGTCCA CAGATGCACCCCACCATGCCTGGCTAACTTTTTTATTTTTTGTAGCAGTCTCACTGTGTTGTCCA T A AC079305.4 Ensembl:ENSG00000229337 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs981319541 Functional Loss SNV dbSNP153 33..33 33 - - - 40369 RMVar_ID_40369 Human_SNP_ID_103297017 A-to-I Human chr2 - 177179806 177179806 177179806 CAGATGCACCCCACCATGCCTGGCTAACTTTTATATTTTTTGTAGCAGTCTCACTGTGTTGTCCA CAGATGCACCCCACCATGCCTGGCTAACTTTTGTATTTTTTGTAGCAGTCTCACTGTGTTGTCCA T C AC079305.4 Ensembl:ENSG00000229337 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs981319541 Functional Loss SNV dbSNP153 33..33 33 - - - 40370 RMVar_ID_40370 Human_SNP_ID_103304041 A-to-I Human chr2 - 177209139 177209139 177209139 GGCGTGCATCACCACGCCTGGCTAATTTTTGTATTTTTAGTGGAGACAGGGTTTCACCATGTTGG GGCGTGCATCACCACGCCTGGCTAATTTTTGTGTTTTTAGTGGAGACAGGGTTTCACCATGTTGG T C AC079305.4 Ensembl:ENSG00000229337 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1157651472 Functional Loss SNV dbSNP153 33..33 33 - - - 40371 RMVar_ID_40371 Human_SNP_ID_103304565 A-to-I Human chr2 - 177210746 177210746 177210746 GGCAGGTCACCTGAGGTGGAGAGTTTGAGACCAGCTTGACCAACACGGTTAAACCCTGTCTCTAC GGCAGGTCACCTGAGGTGGAGAGTTTGAGACCGGCTTGACCAACACGGTTAAACCCTGTCTCTAC T C AC079305.4 Ensembl:ENSG00000229337 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs577316484 Functional Loss SNV dbSNP153 33..33 33 - - - 40372 RMVar_ID_40372 Human_SNP_ID_103305945 A-to-I Human chr2 + 177214540 177214540 177214540 TGTATGGGCCGGGCGCTGTGGCTCACGCCTGTAATTCTAGCACTTTGGGAGGCCGAGGCGGGCGG TGTATGGGCCGGGCGCTGTGGCTCACGCCTGTCATTCTAGCACTTTGGGAGGCCGAGGCGGGCGG A C HNRNPA3 Ensembl:ENSG00000170144 Protein coding intron GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-Seq:(High) rs376838517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_778320,Human_RBP_ID_26787268 40373 RMVar_ID_40373 Human_SNP_ID_103306231 A-to-I Human chr2 + 177215278 177215278 177215278 CACCACGCCCAGCTAATTTTTGTGTTTTTAGTAGAGATGGGGTTTCGCCGTGTTGGCCAGGCTGG CACCACGCCCAGCTAATTTTTGTGTTTTTAGTGGAGATGGGGTTTCGCCGTGTTGGCCAGGCTGG A G HNRNPA3 Ensembl:ENSG00000170144 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs951933875 Functional Loss SNV dbSNP153 33..33 33 - - - 40374 RMVar_ID_40374 Human_SNP_ID_103308538 A-to-I Human chr2 - 177222714 177222714 177222714 GGCAGTCAGCTCACTGCAGCCTCGACTGCCTGATATCAAGGCAGCCTCCCAAATAGCTGGGACTA GGCAGTCAGCTCACTGCAGCCTCGACTGCCTGGTATCAAGGCAGCCTCCCAAATAGCTGGGACTA T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1354597229 Functional Loss SNV dbSNP153 33..33 33 - - - 40375 RMVar_ID_40375 Human_SNP_ID_103309682 A-to-I Human chr2 + 177225877 177225875 177225877 TCAGGAGGTGGAGCTTGCAGTGAGCCAAGATCACACCACTGCACTCCAGCCGGGCAACAGAGCAA TCAGGAGGTGGAGCTTGCAGTGAGCCAAGAT__CACCACTGCACTCCAGCCGGGCAACAGAGCAA TCA T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1431582548 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_6856347,Human_RBP_ID_25487760 40376 RMVar_ID_40376 Human_SNP_ID_103309683 A-to-I Human chr2 + 177225877 177225877 177225877 TCAGGAGGTGGAGCTTGCAGTGAGCCAAGATCACACCACTGCACTCCAGCCGGGCAACAGAGCAA TCAGGAGGTGGAGCTTGCAGTGAGCCAAGATCGCACCACTGCACTCCAGCCGGGCAACAGAGCAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1375041432 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6856347,Human_RBP_ID_25487760 40377 RMVar_ID_40377 Human_SNP_ID_103312250 A-to-I Human chr2 - 177234924 177234923 177234924 TTTAGTAGAGACGTGGTTTCACCATGTTGGCCAGGCTGATCTCGAACTCCAGACCTCAGGTGATC TTTAGTAGAGACGTGGTTTCACCATGTTGGCC_GGCTGATCTCGAACTCCAGACCTCAGGTGATC CT C NFE2L2 Ensembl:ENSG00000116044 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1240386906 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_107949,RMVar_hsa_circ_204828 40378 RMVar_ID_40378 Human_SNP_ID_103312422 A-to-I Human chr2 - 177235608 177235608 177235608 GTGCCCAGGCTAGTAACTCCTGTGCTCCAGCAATCCTCCTGCCTTGGCCTCCCAAACTCCTGGGA GTGCCCAGGCTAGTAACTCCTGTGCTCCAGCAGTCCTCCTGCCTTGGCCTCCCAAACTCCTGGGA T C NFE2L2 Ensembl:ENSG00000116044 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1164466905 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23840007 RMVar_hsa_circ_107949,RMVar_hsa_circ_204828 40379 RMVar_ID_40379 Human_SNP_ID_103312440 A-to-I Human chr2 - 177235705 177235705 177235705 CTCTCACTTCAGTCTCCCTAATAGTTGGGACTACAGGCTCGTATCACCACGTGCAACTAATTTGT CTCTCACTTCAGTCTCCCTAATAGTTGGGACTGCAGGCTCGTATCACCACGTGCAACTAATTTGT T C NFE2L2 Ensembl:ENSG00000116044 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs930199237 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107949,RMVar_hsa_circ_204828 40380 RMVar_ID_40380 Human_SNP_ID_103312459 A-to-I Human chr2 - 177235800 177235800 177235800 TTTGTGTGTGTGAAACAGGGTCTTGTCACCCAAGCTGGAGTGCAGTGGTACAATCACAGCTCACC TTTGTGTGTGTGAAACAGGGTCTTGTCACCCAGGCTGGAGTGCAGTGGTACAATCACAGCTCACC T C NFE2L2 Ensembl:ENSG00000116044 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1156600762 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13695824 RMVar_hsa_circ_107949,RMVar_hsa_circ_204828 40381 RMVar_ID_40381 Human_SNP_ID_103314313 A-to-I Human chr2 - 177244066 177244066 177244066 TCAATCTCCTGATCCTGTGATCCACCTACCTCAGCCTCCTAAAGTGCTGGGATTACAGGCGTGAG TCAATCTCCTGATCCTGTGATCCACCTACCTCTGCCTCCTAAAGTGCTGGGATTACAGGCGTGAG T A NFE2L2 Ensembl:ENSG00000116044 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1269368572 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107949,RMVar_hsa_circ_204828 40382 RMVar_ID_40382 Human_SNP_ID_103314955 A-to-I Human chr2 - 177246724 177246724 177246724 ATAGTGGCACATGCCTGTAATCTCAGCTATTCAGGAGGCTGAGGTGGGAAGATTGCTTGAGCCCA ATAGTGGCACATGCCTGTAATCTCAGCTATTCGGGAGGCTGAGGTGGGAAGATTGCTTGAGCCCA T C NFE2L2 Ensembl:ENSG00000116044 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1426264896 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107949,RMVar_hsa_circ_204828 40383 RMVar_ID_40383 Human_SNP_ID_103315442 A-to-I Human chr2 - 177248570 177248570 177248570 ACCCTGTCTCTACTAAAAATGCAAAATTGGCCAGGCATGGTGGCGCATGCCTGTAATCCAAGCTA ACCCTGTCTCTACTAAAAATGCAAAATTGGCCTGGCATGGTGGCGCATGCCTGTAATCCAAGCTA T A NFE2L2 Ensembl:ENSG00000116044 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs768980715 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17570064 RMVar_hsa_circ_107949,RMVar_hsa_circ_204828 40384 RMVar_ID_40384 Human_SNP_ID_103315470 A-to-I Human chr2 - 177248676 177248676 177248676 GGCCAGAGGCGGTGGCTCATGCCTGTAATGCCAGCACTTTGGGAGGCCCAGGCAGGCGGATCACC GGCCAGAGGCGGTGGCTCATGCCTGTAATGCCGGCACTTTGGGAGGCCCAGGCAGGCGGATCACC T C NFE2L2 Ensembl:ENSG00000116044 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1196174913 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107949,RMVar_hsa_circ_204828 40385 RMVar_ID_40385 Human_SNP_ID_103319469 A-to-I Human chr2 + 177265013 177265012 177265014 GCAAATAAGGGCAGCGCTCTCGCCCGCGAGATAAAGAGTTGTTTGCGAAGGTCGCTGGAGTTCGG GCAAATAAGGGCAGCGCTCTCGCCCGCGAGAT__AGAGTTGTTTGCGAAGGTCGCTGGAGTTCGG TAA T AC079305.2 Ensembl:ENSG00000222043 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs200432479 Functional Loss DEL dbSNP153 33..34 33 - - - 40386 RMVar_ID_40386 Human_SNP_ID_103319471 A-to-I Human chr2 + 177265013 177265013 177265013 GCAAATAAGGGCAGCGCTCTCGCCCGCGAGATAAAGAGTTGTTTGCGAAGGTCGCTGGAGTTCGG GCAAATAAGGGCAGCGCTCTCGCCCGCGAGATGAAGAGTTGTTTGCGAAGGTCGCTGGAGTTCGG A G AC079305.2 Ensembl:ENSG00000222043 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs557247518 Functional Loss SNV dbSNP153 33..33 33 - - - 40387 RMVar_ID_40387 Human_SNP_ID_103326908 A-to-I Human chr2 + 177297038 177297038 177297038 CTCCTGCCTCAGCCTCCCAAGTAGCTGAGATCACAGGTACCCGCCTCCATGCCTGGCTAATTTTT CTCCTGCCTCAGCCTCCCAAGTAGCTGAGATCGCAGGTACCCGCCTCCATGCCTGGCTAATTTTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1371520975 Functional Loss SNV dbSNP153 33..33 33 - - - 40388 RMVar_ID_40388 Human_SNP_ID_103326925 A-to-I Human chr2 + 177297130 177297130 177297130 ATTGGTCAGGCTGATTTCAAACTCCTGACCTCAAGTGATCTTCCCGCCTCAGCCTCTCAAAGTAG ATTGGTCAGGCTGATTTCAAACTCCTGACCTCGAGTGATCTTCCCGCCTCAGCCTCTCAAAGTAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1363403263 Functional Loss SNV dbSNP153 33..33 33 - - - 40389 RMVar_ID_40389 Human_SNP_ID_103328604 A-to-I Human chr2 + 177304277 177304277 177304277 TTTTAAAAATACATAGTTTTCTGGCCCAGTGCAGTGGTTAACACCTGTAATCCCAACACTTTGGG TTTTAAAAATACATAGTTTTCTGGCCCAGTGCCGTGGTTAACACCTGTAATCCCAACACTTTGGG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs925291603 Functional Loss SNV dbSNP153 33..33 33 - - - 40390 RMVar_ID_40390 Human_SNP_ID_103330195 A-to-I Human chr2 - 177311452 177311452 177311452 GTCGCCATGCTGGAGTGCAGTGGCACGATCTCAGCTCACTGCAACCTCTGCTTCCAGGGTTCAAG GTCGCCATGCTGGAGTGCAGTGGCACGATCTCGGCTCACTGCAACCTCTGCTTCCAGGGTTCAAG T C NFE2L2,AC019080.1 Ensembl:ENSG00000116044,Ensembl:ENSG00000213963 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1275033369 Functional Loss SNV dbSNP153 33..33 33 - - - 40391 RMVar_ID_40391 Human_SNP_ID_103330684 A-to-I Human chr2 + 177313493 177313493 177313493 GAGAAAGATTCTTGTTCTGTCCAGGCTGGAGTACAGTGGCACAATCACAACTCACTGCAGCCTAG GAGAAAGATTCTTGTTCTGTCCAGGCTGGAGTGCAGTGGCACAATCACAACTCACTGCAGCCTAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1213609674 Functional Loss SNV dbSNP153 33..33 33 - - - 40392 RMVar_ID_40392 Human_SNP_ID_103332031 A-to-I Human chr2 - 177320106 177320104 177320106 GGCATAAAATTCGGCTGGGTATGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGTTGAGGT GGCATAAAATTCGGCTGGGTATGGTGGCTCAC__CTGTAATCCCAGCACTTTGGGAGGTTGAGGT GGT G NFE2L2,AC019080.1 Ensembl:ENSG00000116044,Ensembl:ENSG00000213963 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285732701 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_26486770 40393 RMVar_ID_40393 Human_SNP_ID_103332268 A-to-I Human chr2 - 177321252 177321252 177321252 CCTCAAGTGATCCTCCCAACTCAGCCTCCCAAAGTATTGGAATTATAGGTGTGAGCCACTACACC CCTCAAGTGATCCTCCCAACTCAGCCTCCCAATGTATTGGAATTATAGGTGTGAGCCACTACACC T A NFE2L2,AC019080.1 Ensembl:ENSG00000116044,Ensembl:ENSG00000213963 Protein coding,lincRNA intron,intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line - 29129909,31158229,32596459 RNA-Seq:(High) rs964830503 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_539088,Human_RBP_ID_8203525,Human_RBP_ID_26487539 40394 RMVar_ID_40394 Human_SNP_ID_103332274 A-to-I Human chr2 - 177321279 177321279 177321279 TTGCCCAGGCTGGTCTTGAACTTCTGGCCTCAAGTGATCCTCCCAACTCAGCCTCCCAAAGTATT TTGCCCAGGCTGGTCTTGAACTTCTGGCCTCAGGTGATCCTCCCAACTCAGCCTCCCAAAGTATT T C NFE2L2,AC019080.1 Ensembl:ENSG00000116044,Ensembl:ENSG00000213963 Protein coding,lincRNA intron,intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1264025728 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_539088,Human_RBP_ID_26487539 40395 RMVar_ID_40395 Human_SNP_ID_103332275 A-to-I Human chr2 - 177321280 177321280 177321280 GTTGCCCAGGCTGGTCTTGAACTTCTGGCCTCAAGTGATCCTCCCAACTCAGCCTCCCAAAGTAT GTTGCCCAGGCTGGTCTTGAACTTCTGGCCTCGAGTGATCCTCCCAACTCAGCCTCCCAAAGTAT T C NFE2L2,AC019080.1 Ensembl:ENSG00000116044,Ensembl:ENSG00000213963 Protein coding,lincRNA intron,intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs992002650 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_539088,Human_RBP_ID_26487539 40396 RMVar_ID_40396 Human_SNP_ID_103332450 A-to-I Human chr2 - 177321990 177321990 177321990 GTGATCCACCCATCTCGGCCTCCCAAAGTGCTAGGATTACAGGCATGAGCCACCACGCCCAGCCA GTGATCCACCCATCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCACGCCCAGCCA T C NFE2L2,AC019080.1 Ensembl:ENSG00000116044,Ensembl:ENSG00000213963 Protein coding,lincRNA intron,intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1329548137 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_145294 40397 RMVar_ID_40397 Human_SNP_ID_103341957 A-to-I Human chr2 - 177361030 177361030 177361030 TCTAAAAGAACTCAGGCTAGGTGCAATGGCTTACACCTGTAATCCTAGCACTTTGGGAGGCCAAG TCTAAAAGAACTCAGGCTAGGTGCAATGGCTTGCACCTGTAATCCTAGCACTTTGGGAGGCCAAG T C NFE2L2,AC019080.1 Ensembl:ENSG00000116044,Ensembl:ENSG00000213963 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1199805014 Functional Loss SNV dbSNP153 33..33 33 - - - 40398 RMVar_ID_40398 Human_SNP_ID_103347288 A-to-I Human chr2 - 177385324 177385324 177385324 TCACTGTAACCTGGAACTCCTGGGTTCAGGCAATCTTCCCACTTCAGCTTCCTGAGTAGCTAGAA TCACTGTAACCTGGAACTCCTGGGTTCAGGCAGTCTTCCCACTTCAGCTTCCTGAGTAGCTAGAA T C NFE2L2,AC019080.1 Ensembl:ENSG00000116044,Ensembl:ENSG00000213963 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1336442071 Functional Loss SNV dbSNP153 33..33 33 - - - 40399 RMVar_ID_40399 Human_SNP_ID_103347289 A-to-I Human chr2 - 177385329 177385329 177385329 ATAGGTCACTGTAACCTGGAACTCCTGGGTTCAGGCAATCTTCCCACTTCAGCTTCCTGAGTAGC ATAGGTCACTGTAACCTGGAACTCCTGGGTTCTGGCAATCTTCCCACTTCAGCTTCCTGAGTAGC T A NFE2L2,AC019080.1 Ensembl:ENSG00000116044,Ensembl:ENSG00000213963 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474953000 Functional Loss SNV dbSNP153 33..33 33 - - - 40400 RMVar_ID_40400 Human_SNP_ID_103347298 A-to-I Human chr2 - 177385359 177385359 177385359 ACTCTGTCGCCGGAGGGCAGTGGCATGATCATAGGTCACTGTAACCTGGAACTCCTGGGTTCAGG ACTCTGTCGCCGGAGGGCAGTGGCATGATCATCGGTCACTGTAACCTGGAACTCCTGGGTTCAGG T G NFE2L2,AC019080.1 Ensembl:ENSG00000116044,Ensembl:ENSG00000213963 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1395471695 Functional Loss SNV dbSNP153 33..33 33 - - - 40401 RMVar_ID_40401 Human_SNP_ID_103349981 A-to-I Human chr2 + 177396987 177396987 177396987 TTGCTATGGAGTCTTGCTCTGTCTCCCAGGCTAGAGTGAAGTGGCGCGATCTCAGCTCACTGCAA TTGCTATGGAGTCTTGCTCTGTCTCCCAGGCTGGAGTGAAGTGGCGCGATCTCAGCTCACTGCAA A G AGPS Ensembl:ENSG00000018510 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1197536756 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76064,RMVar_hsa_circ_204829 40402 RMVar_ID_40402 Human_SNP_ID_103370346 A-to-I Human chr2 + 177485603 177485603 177485603 AAAAAAATTCTTAGGATGTTCACCCAATGACTATAATCTAAATTCACTACACAAAACTATAGTGA AAAAAAATTCTTAGGATGTTCACCCAATGACTGTAATCTAAATTCACTACACAAAACTATAGTGA A G AGPS Ensembl:ENSG00000018510 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs868725046 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27512,RMVar_hsa_circ_60801,RMVar_hsa_circ_5838,RMVar_hsa_circ_97080,RMVar_hsa_circ_40857,RMVar_hsa_circ_204836,RMVar_hsa_circ_377474,RMVar_hsa_circ_34166,RMVar_hsa_circ_31164,RMVar_hsa_circ_204840,RMVar_hsa_circ_366652,RMVar_hsa_circ_370549,RMVar_hsa_circ_369977,RMVar_hsa_circ_58040,RMVar_hsa_circ_67743,RMVar_hsa_circ_204841,RMVar_hsa_circ_105622,RMVar_hsa_circ_367510,RMVar_hsa_circ_294916,RMVar_hsa_circ_204844,RMVar_hsa_circ_204845,RMVar_hsa_circ_365755,RMVar_hsa_circ_74739,RMVar_hsa_circ_204846,RMVar_hsa_circ_204848,RMVar_hsa_circ_280121,RMVar_hsa_circ_334426,RMVar_hsa_circ_334820,RMVar_hsa_circ_296904,RMVar_hsa_circ_75419,RMVar_hsa_circ_204847 40403 RMVar_ID_40403 Human_SNP_ID_103379561 A-to-I Human chr2 + 177526427 177526427 177526427 AATTCTTGTATTTTTAGTAGAGACGGGTTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGA AATTCTTGTATTTTTAGTAGAGACGGGTTTTCTCCATGTTGGCCAGGCTGGTCTCGAACTCCTGA A T AGPS Ensembl:ENSG00000018510 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1214560079 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97080,RMVar_hsa_circ_204836,RMVar_hsa_circ_119168,RMVar_hsa_circ_204850,RMVar_hsa_circ_114301,RMVar_hsa_circ_204853,RMVar_hsa_circ_91502,RMVar_hsa_circ_204854,RMVar_hsa_circ_82308,RMVar_hsa_circ_204856 40404 RMVar_ID_40404 Human_SNP_ID_103387362 A-to-I Human chr2 + 177561142 177561142 177561142 TTGTATGTTTAGTAGAGATGGGGTTTCACCATATTGACCAAATTGGTCTCAAACTCCTGACCTCA TTGTATGTTTAGTAGAGATGGGGTTTCACCATGTTGACCAAATTGGTCTCAAACTCCTGACCTCA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1192598397 Functional Loss SNV dbSNP153 33..33 33 - - - 40405 RMVar_ID_40405 Human_SNP_ID_103404143 A-to-I Human chr2 - 177627308 177627308 177627308 GTATAGACCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCAATTTGGAAGGCCGAGGCGGGCGGA GTATAGACCGGGCGCGGTGGCTCACGCCTGTAGTCCCAGCAATTTGGAAGGCCGAGGCGGGCGGA T C PDE11A Ensembl:ENSG00000128655 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1255913451 Functional Loss SNV dbSNP153 33..33 33 - - - 40406 RMVar_ID_40406 Human_SNP_ID_103516406 A-to-I Human chr2 + 178114817 178114817 178114817 CAGGGTCTCACTATGTTGCCTAAGCAGGTCTCAAGCTCCTGGACTCAAGTGAGCCTCCCGTTTCA CAGGGTCTCACTATGTTGCCTAAGCAGGTCTCCAGCTCCTGGACTCAAGTGAGCCTCCCGTTTCA A C RBM45 Ensembl:ENSG00000155636 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1441480348 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_204863,RMVar_hsa_circ_83979 40407 RMVar_ID_40407 Human_SNP_ID_103576309 A-to-I Human chr2 + 178369071 178369071 178369071 CATCTGCCTTGGTCTCCCAAAGTGCTGAGGTTACAGACATGAGCCACCACACCCAGCCTTCATCT CATCTGCCTTGGTCTCCCAAAGTGCTGAGGTTGCAGACATGAGCCACCACACCCAGCCTTCATCT A G OSBPL6 Ensembl:ENSG00000079156 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs894883160 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40590,RMVar_hsa_circ_82618,RMVar_hsa_circ_204869,RMVar_hsa_circ_71282,RMVar_hsa_circ_266278,RMVar_hsa_circ_350100 40408 RMVar_ID_40408 Human_SNP_ID_103576310 A-to-I Human chr2 + 178369071 178369071 178369071 CATCTGCCTTGGTCTCCCAAAGTGCTGAGGTTACAGACATGAGCCACCACACCCAGCCTTCATCT CATCTGCCTTGGTCTCCCAAAGTGCTGAGGTTTCAGACATGAGCCACCACACCCAGCCTTCATCT A T OSBPL6 Ensembl:ENSG00000079156 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs894883160 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40590,RMVar_hsa_circ_82618,RMVar_hsa_circ_204869,RMVar_hsa_circ_71282,RMVar_hsa_circ_266278,RMVar_hsa_circ_350100 40409 RMVar_ID_40409 Human_SNP_ID_103591314 A-to-I Human chr2 + 178434134 178434133 178434135 TCAGCCACCTTTTCTTTTTTTTTTTTTGAGACAGAGTCTCACTCTGTCACTCAGGCTGGAGTGCA TCAGCCACCTTTTCTTTTTTTTTTTTTGAGAC__AGTCTCACTCTGTCACTCAGGCTGGAGTGCA CAG C CHROMR Ensembl:ENSG00000223960 lincRNA intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1559351427 Functional Loss DEL dbSNP153 33..34 33 - - - 40410 RMVar_ID_40410 Human_SNP_ID_103591365 A-to-I Human chr2 + 178434276 178434276 178434276 GGGATTACAGGTGCACGCCACCTTGTCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCA GGGATTACAGGTGCACGCCACCTTGTCTGGCTGATTTTTGTATTTTTAGTAGAGACAGGGTTTCA A G CHROMR Ensembl:ENSG00000223960 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350791824 Functional Loss SNV dbSNP153 33..33 33 - - - 40411 RMVar_ID_40411 Human_SNP_ID_103591371 A-to-I Human chr2 + 178434291 178434291 178434291 CGCCACCTTGTCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCGTGTTGGTCAGGC CGCCACCTTGTCTGGCTAATTTTTGTATTTTTGGTAGAGACAGGGTTTCACCGTGTTGGTCAGGC A G CHROMR Ensembl:ENSG00000223960 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs530780849 Functional Loss SNV dbSNP153 33..33 33 - - - 40412 RMVar_ID_40412 Human_SNP_ID_103591423 A-to-I Human chr2 + 178434473 178434472 178434473 CAAGTCTAACTCTGTCACCCAGGCTGGAGAGCAGCGGCATGATCATGGCTCACTGCTGCCTCAAC CAAGTCTAACTCTGTCACCCAGGCTGGAGAGC_GCGGCATGATCATGGCTCACTGCTGCCTCAAC CA C CHROMR Ensembl:ENSG00000223960 lincRNA intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1462518714 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_1592528,Human_RBP_ID_6857744,Human_RBP_ID_13699606 40413 RMVar_ID_40413 Human_SNP_ID_103591431 A-to-I Human chr2 + 178434548 178434544 178434549 CAAGTCATTGTCCCCACCTCAGCCTCCCTAGTAGACTGGACTACAGGCATGTGCCACCACACCCA CAAGTCATTGTCCCCACCTCAGCCTCCCT_____ACTGGACTACAGGCATGTGCCACCACACCCA TAGTAG T CHROMR Ensembl:ENSG00000223960 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1333735877 Functional Loss DEL dbSNP153 30..34 33 - - - Human_RBP_ID_13699610,Human_RBP_ID_22371252,Human_RBP_ID_27476186 40414 RMVar_ID_40414 Human_SNP_ID_103591498 A-to-I Human chr2 + 178434847 178434847 178434847 ACACATGTTAAATCAAGATACTTTGGCCAGGCACGGTGGCTCACACCTGTAATCCCAGCACTTTG ACACATGTTAAATCAAGATACTTTGGCCAGGCGCGGTGGCTCACACCTGTAATCCCAGCACTTTG A G CHROMR Ensembl:ENSG00000223960 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs563531404 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17945239 40415 RMVar_ID_40415 Human_SNP_ID_103591544 A-to-I Human chr2 + 178435033 178435033 178435033 GAGGTCAGGAGTTTGAGACCAGCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATGCAAA GAGGTCAGGAGTTTGAGACCAGCCTGGCCAACGTGGTGAAACCCCGTCTCTACTAAAAATGCAAA A G CHROMR Ensembl:ENSG00000223960 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1210462068 Functional Loss SNV dbSNP153 33..33 33 - - - 40416 RMVar_ID_40416 Human_SNP_ID_103591559 A-to-I Human chr2 + 178435096 178435096 178435096 AAAATTAGGTGGGTGTGGTGGCACACAGCAGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGA AAAATTAGGTGGGTGTGGTGGCACACAGCAGTGGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGA A G CHROMR Ensembl:ENSG00000223960 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs948704566 Functional Loss SNV dbSNP153 33..33 33 - - - 40417 RMVar_ID_40417 Human_SNP_ID_103591565 A-to-I Human chr2 + 178435137 178435137 178435137 TACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAACCTGGGAGGCAGAGGTTACAGTGAGCTGAGA TACTCAGGAGGCTGAGGCAGGAGAATTGCTTGCACCTGGGAGGCAGAGGTTACAGTGAGCTGAGA A C CHROMR Ensembl:ENSG00000223960 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1044483393 Functional Loss SNV dbSNP153 33..33 33 - - - 40418 RMVar_ID_40418 Human_SNP_ID_103591591 A-to-I Human chr2 + 178435262 178435262 178435262 AAAATTAGCCAGGCTTGGTGGTGGATGCCTGTATTCCCAGCTTCTTGGGAGACTGAAGCAGGAGG AAAATTAGCCAGGCTTGGTGGTGGATGCCTGTGTTCCCAGCTTCTTGGGAGACTGAAGCAGGAGG A G CHROMR Ensembl:ENSG00000223960 lincRNA intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1138261 Functional Loss SNV dbSNP153 33..33 33 - - - 40419 RMVar_ID_40419 Human_SNP_ID_103591608 A-to-I Human chr2 + 178435333 178435333 178435333 TGAACCCAGGAGGCAGAGGTTGCAGTGAGTTGAGATTGTGCCACTGTACTCCAGCCTGGGCAACA TGAACCCAGGAGGCAGAGGTTGCAGTGAGTTGCGATTGTGCCACTGTACTCCAGCCTGGGCAACA A C CHROMR Ensembl:ENSG00000223960 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs148697545 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25488885 40420 RMVar_ID_40420 Human_SNP_ID_103594139 A-to-I Human chr2 - 178445664 178445664 178445664 CCCCACTGGTGATGGCCATGCTGTTTCTGTATAGCCTGAAGGTGAACCCAACCATTAAGTACATT CCCCACTGGTGATGGCCATGCTGTTTCTGTATTGCCTGAAGGTGAACCCAACCATTAAGTACATT T A PRKRA Ensembl:ENSG00000180228 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1029607835 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13699816 RMVar_hsa_circ_53641,RMVar_hsa_circ_267225 40421 RMVar_ID_40421 Human_SNP_ID_103594186 A-to-I Human chr2 - 178445869 178445869 178445869 AAAATTAGCCGAGTGTGGTGGCACGCTCCTGTAATCCCAGCTGCTTGGGAGGCTGAGACACGAGA AAAATTAGCCGAGTGTGGTGGCACGCTCCTGTGATCCCAGCTGCTTGGGAGGCTGAGACACGAGA T C PRKRA Ensembl:ENSG00000180228 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1015377713 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_53641,RMVar_hsa_circ_267225 40422 RMVar_ID_40422 Human_SNP_ID_103594217 A-to-I Human chr2 - 178445973 178445973 178445973 TAATCCCAGCACTTTGGGAGGCCAAGGTGGGCAGATCACTTGAGTCAGGAGTTCGAGACCAGCCT TAATCCCAGCACTTTGGGAGGCCAAGGTGGGCGGATCACTTGAGTCAGGAGTTCGAGACCAGCCT T C PRKRA Ensembl:ENSG00000180228 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1197230546 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_53641,RMVar_hsa_circ_267225 40423 RMVar_ID_40423 Human_SNP_ID_103776589 A-to-I Human chr2 - 179105635 179105635 179105635 ATCATTGCTATAATTATCTTTTCAGAATAAAAAATAGAGTATTCTTTATCCTTTCTGTTGTCTCA ATCATTGCTATAATTATCTTTTCAGAATAAAAGATAGAGTATTCTTTATCCTTTCTGTTGTCTCA T C SESTD1 Ensembl:ENSG00000187231 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1168333025 Functional Loss SNV dbSNP153 33..33 33 - - - 40424 RMVar_ID_40424 Human_SNP_ID_103790638 A-to-I Human chr2 - 179161037 179161037 179161037 TATGGTGGTGCATACCTGTATTCCTAGTTACTAGGAAGGCTGAGAAGGGAGGATCACTTGAGCTG TATGGTGGTGCATACCTGTATTCCTAGTTACTGGGAAGGCTGAGAAGGGAGGATCACTTGAGCTG T C SESTD1 Ensembl:ENSG00000187231 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs554071570 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26659,RMVar_hsa_circ_8245,RMVar_hsa_circ_71932,RMVar_hsa_circ_41434,RMVar_hsa_circ_308463,RMVar_hsa_circ_358523,RMVar_hsa_circ_46614,RMVar_hsa_circ_116644,RMVar_hsa_circ_204929,RMVar_hsa_circ_19799,RMVar_hsa_circ_204931 40425 RMVar_ID_40425 Human_SNP_ID_103924684 A-to-I Human chr2 - 179720833 179720833 179720833 ATCACTTGAGCCCAGGAATTCAAGGTTATAGTAAGTGTGATTACATCACTGCATTCCAGCCTGGG ATCACTTGAGCCCAGGAATTCAAGGTTATAGTGAGTGTGATTACATCACTGCATTCCAGCCTGGG T C ZNF385B Ensembl:ENSG00000144331 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1300744419 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25489940 RMVar_hsa_circ_32608,RMVar_hsa_circ_204941 40426 RMVar_ID_40426 Human_SNP_ID_103978120 A-to-I Human chr2 - 179946375 179946375 179946375 GCATTCTTGGCGTACTGCAACCTCTGCCTCCCAGGCTCAATTGATCCTCCCACCTCAGGCTCCTG GCATTCTTGGCGTACTGCAACCTCTGCCTCCCGGGCTCAATTGATCCTCCCACCTCAGGCTCCTG T C CWC22 Ensembl:ENSG00000163510 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947050858 Functional Loss SNV dbSNP153 33..33 33 - - - 40427 RMVar_ID_40427 Human_SNP_ID_715794152 A-to-I Human chrX - 45785738 45785738 45785738 GAATATGTAAATATTGGCCTGAAAATATTTACATATTCAATTGCTTATCTATTTTCCTATTGATC GAATATGTAAATATTGGCCTGAAAATATTTACGTATTCAATTGCTTATCTATTTTCCTATTGATC T C LINC02595 RNACentral:URS00009B5DC4 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1342727299 Functional Loss SNV dbSNP153 33..33 33 - - - 40428 RMVar_ID_40428 Human_SNP_ID_715799447 A-to-I Human chrX - 45817080 45817068 45817081 CAAACAGACACACACCAGTACAAAAATTAGCCAGGCGTGGTAGCACACATCTGTAGGCTCAGCTA CAAACAGACACACACCAGTACAAAAATTAGC_____________ACACATCTGTAGGCTCAGCTA TGCTACCACGCCTG T LINC02595 RNACentral:URS00009B5DC4 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs782053132 Functional Loss DEL dbSNP153 32..44 33 - - - 40429 RMVar_ID_40429 Human_SNP_ID_715799448 A-to-I Human chrX - 45817071 45817071 45817071 ACACACCAGTACAAAAATTAGCCAGGCGTGGTAGCACACATCTGTAGGCTCAGCTACAGAGGCTG ACACACCAGTACAAAAATTAGCCAGGCGTGGTGGCACACATCTGTAGGCTCAGCTACAGAGGCTG T C LINC02595 RNACentral:URS00009B5DC4 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1555943563 Functional Loss SNV dbSNP153 33..33 33 - - - 40430 RMVar_ID_40430 Human_SNP_ID_715803932 A-to-I Human chrX - 45844482 45844482 45844482 TCAAGTGATCCTCCTTCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCATGTGACACCATGCCTA TCAAGTGATCCTCCTTCCTCAGCCTCCCAAGTTGCTGGGACTACAGGCATGTGACACCATGCCTA T A LINC02595,LINC02595:2 RNACentral:URS00009B5DC4,RNACentral:URS00009C28A8 lincRNA,lincRNA exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1555946542 Functional Loss SNV dbSNP153 33..33 33 - - - 40431 RMVar_ID_40431 Human_SNP_ID_715804097 A-to-I Human chrX - 45845499 45845499 45845499 GAACTCCTGACCTCAGGTGATCCACCTGCCTCAGCCCACCAAAGTGCTGGGATTACAGGCGTGAG GAACTCCTGACCTCAGGTGATCCACCTGCCTCCGCCCACCAAAGTGCTGGGATTACAGGCGTGAG T G LINC02595,LINC02595:2 RNACentral:URS00009B5DC4,RNACentral:URS00009C28A8 lincRNA,lincRNA exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1555946634 Functional Loss SNV dbSNP153 33..33 33 - - - 40432 RMVar_ID_40432 Human_SNP_ID_715804420 A-to-I Human chrX - 45847192 45847192 45847192 GGTGATGTGCACCTGTAGCTATGTGTACCTGTAGTCCCACACAGTCGGGAGGCTGAGGTGGGAGC GGTGATGTGCACCTGTAGCTATGTGTACCTGTGGTCCCACACAGTCGGGAGGCTGAGGTGGGAGC T C LINC02595 Ensembl:ENSG00000231566 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1196147858 Functional Loss SNV dbSNP153 33..33 33 - - - 40433 RMVar_ID_40433 Human_SNP_ID_715804422 A-to-I Human chrX - 45847198 45847198 45847198 AGGCGTGGTGATGTGCACCTGTAGCTATGTGTACCTGTAGTCCCACACAGTCGGGAGGCTGAGGT AGGCGTGGTGATGTGCACCTGTAGCTATGTGTTCCTGTAGTCCCACACAGTCGGGAGGCTGAGGT T A LINC02595 Ensembl:ENSG00000231566 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs781954193 Functional Loss SNV dbSNP153 33..33 33 - - - 40434 RMVar_ID_40434 Human_SNP_ID_715804423 A-to-I Human chrX - 45847198 45847198 45847198 AGGCGTGGTGATGTGCACCTGTAGCTATGTGTACCTGTAGTCCCACACAGTCGGGAGGCTGAGGT AGGCGTGGTGATGTGCACCTGTAGCTATGTGTGCCTGTAGTCCCACACAGTCGGGAGGCTGAGGT T C LINC02595 Ensembl:ENSG00000231566 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs781954193 Functional Loss SNV dbSNP153 33..33 33 - - - 40435 RMVar_ID_40435 Human_SNP_ID_715804521 A-to-I Human chrX - 45847798 45847798 45847798 CGATTCCCCTGCCCCAGCCTCCTGAGTGGCTGAGATTACAGGCACCCACCACCAGGCCCGGCTAA CGATTCCCCTGCCCCAGCCTCCTGAGTGGCTGGGATTACAGGCACCCACCACCAGGCCCGGCTAA T C LINC02595 Ensembl:ENSG00000231566 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1424409039 Functional Loss SNV dbSNP153 33..33 33 - - - 40436 RMVar_ID_40436 Human_SNP_ID_715822402 A-to-I Human chrX - 45952188 45952188 45952188 GTACTTTGGTGGTTGACTTGGAGTCATCTTTCAAGGCTTGCTTTGTATCTCTGGTGAGTCAGGAC GTACTTTGGTGGTTGACTTGGAGTCATCTTTCTAGGCTTGCTTTGTATCTCTGGTGAGTCAGGAC T A MED28P4 Ensembl:ENSG00000224701 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1291554440 Functional Loss SNV dbSNP153 33..33 33 - - - 40437 RMVar_ID_40437 Human_SNP_ID_715883569 A-to-I Human chrX + 46288251 46288251 46288251 GGGTACATGGTAGTGCCGCCAGACAGCACTGTATTGGCGTACAGGTCTTTGCAGATGTCCACATC GGGTACATGGTAGTGCCGCCAGACAGCACTGTGTTGGCGTACAGGTCTTTGCAGATGTCCACATC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs745831886 Functional Loss SNV dbSNP153 33..33 33 - - - 40438 RMVar_ID_40438 Human_SNP_ID_715914619 A-to-I Human chrX + 46459154 46459154 46459154 GGCCAACATGGTGAAACCCTGTCTCTACTAAAAATACAAAAAATTAGCCAGGCATGGTGGCGCAT GGCCAACATGGTGAAACCCTGTCTCTACTAAATATACAAAAAATTAGCCAGGCATGGTGGCGCAT A T KRBOX4 Ensembl:ENSG00000147121 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1295190983 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40329,RMVar_hsa_circ_262199,RMVar_hsa_circ_278658 40439 RMVar_ID_40439 Human_SNP_ID_715916921 A-to-I Human chrX + 46473800 46473800 46473800 CCTCAACCTCCCAAATAGTTGGGATTACAGGCACATGCCACCATACGCAGCTAATTTGTATTTTT CCTCAACCTCCCAAATAGTTGGGATTACAGGCTCATGCCACCATACGCAGCTAATTTGTATTTTT A T KRBOX4 Ensembl:ENSG00000147121 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs976713738 Functional Loss SNV dbSNP153 33..33 33 - - - 40440 RMVar_ID_40440 Human_SNP_ID_715920947 A-to-I Human chrX - 46499387 46499387 46499387 AGGCTGAGGTGGGCAGATTGCTTGAGCTCACAAGTTTGAGACCAGCCTGGGCAACATGGCAAAAC AGGCTGAGGTGGGCAGATTGCTTGAGCTCACACGTTTGAGACCAGCCTGGGCAACATGGCAAAAC T G ZNF674 Ensembl:ENSG00000251192 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1569462875 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266007 40441 RMVar_ID_40441 Human_SNP_ID_715928192 A-to-I Human chrX - 46542536 46542536 46542536 TAATTTTTTTAATTTTCGGTTTTGTAGAGACAAGGCCTTGCTATATTGTCTAGGCTGGTCTTGAA TAATTTTTTTAATTTTCGGTTTTGTAGAGACAGGGCCTTGCTATATTGTCTAGGCTGGTCTTGAA T C ZNF674 Ensembl:ENSG00000251192 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1274244689 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16894876 RMVar_hsa_circ_266007,RMVar_hsa_circ_51786,RMVar_hsa_circ_262203,RMVar_hsa_circ_112271 40442 RMVar_ID_40442 Human_SNP_ID_715928203 A-to-I Human chrX - 46542590 46542590 46542590 CCCATCTCAGCCTTTTGAGTAGCTGGGACTACAGGCATGCACCACCACGCCAGCTAATTTTTTTA CCCATCTCAGCCTTTTGAGTAGCTGGGACTACGGGCATGCACCACCACGCCAGCTAATTTTTTTA T C ZNF674 Ensembl:ENSG00000251192 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027892813 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266007,RMVar_hsa_circ_51786,RMVar_hsa_circ_262203,RMVar_hsa_circ_112271 40443 RMVar_ID_40443 Human_SNP_ID_715929088 A-to-I Human chrX + 46547997 46547997 46547997 CCTGGCTAATTTTTTAAATTTTTTGTAGAGATAGTGTCTCGCTATGTTGCCCACGCTGGTCTGGA CCTGGCTAATTTTTTAAATTTTTTGTAGAGATGGTGTCTCGCTATGTTGCCCACGCTGGTCTGGA A G ZNF674-AS1 Ensembl:ENSG00000230844 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355304978 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3257441 40444 RMVar_ID_40444 Human_SNP_ID_715929094 A-to-I Human chrX + 46548008 46548008 46548008 TTTTAAATTTTTTGTAGAGATAGTGTCTCGCTATGTTGCCCACGCTGGTCTGGAATTCCTGGACT TTTTAAATTTTTTGTAGAGATAGTGTCTCGCTGTGTTGCCCACGCTGGTCTGGAATTCCTGGACT A G ZNF674-AS1 Ensembl:ENSG00000230844 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1177324785 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3257441,Human_RBP_ID_16963716 40445 RMVar_ID_40445 Human_SNP_ID_715937894 A-to-I Human chrX - 46603594 46603594 46603594 GACCTCGTGATCCACCCGCCTCTGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCCCC GACCTCGTGATCCACCCGCCTCTGCCTCCCAAGGTGCTGGGATTACAGGCGTGAGCCACCGCCCC T C SLC9A7 Ensembl:ENSG00000065923 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1003614425 Functional Loss SNV dbSNP153 33..33 33 - - - 40446 RMVar_ID_40446 Human_SNP_ID_715937938 A-to-I Human chrX - 46603820 46603820 46603820 TTTTGTTTTGTTTTTAGATGGAGTCTCGCTCTATCCCCCAGGCTGGAGTGCAGTGGCATGACCTC TTTTGTTTTGTTTTTAGATGGAGTCTCGCTCTGTCCCCCAGGCTGGAGTGCAGTGGCATGACCTC T C SLC9A7 Ensembl:ENSG00000065923 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs997243869 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_187533,Human_RBP_ID_5063978,Human_RBP_ID_8004790 40447 RMVar_ID_40447 Human_SNP_ID_715938267 A-to-I Human chrX - 46605974 46605974 46605974 ATTTTTTGTATTTTTGGTAGAGATGGGGTTTCACCATGTTGCCCAGGCTGGTGTCAAACTCCTGA ATTTTTTGTATTTTTGGTAGAGATGGGGTTTCGCCATGTTGCCCAGGCTGGTGTCAAACTCCTGA T C SLC9A7 Ensembl:ENSG00000065923 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1466489869 Functional Loss SNV dbSNP153 33..33 33 - - - 40448 RMVar_ID_40448 Human_SNP_ID_715957645 A-to-I Human chrX + 46725636 46725636 46725636 TTTTGCTTTAAAACTCACGAGGCTTTCTGCTTAACCATACTCTTTGCAGGACCCTCTCTCATCTT TTTTGCTTTAAAACTCACGAGGCTTTCTGCTTGACCATACTCTTTGCAGGACCCTCTCTCATCTT A G RF00017-4498 RNACentral:URS000099B61A SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879035194 Functional Loss SNV dbSNP153 33..33 33 - - - 40449 RMVar_ID_40449 Human_SNP_ID_715957668 A-to-I Human chrX + 46725751 46725751 46725751 TCTTGTCAATGGATTCTGCCCTGCTGTCCACCATGTCAATGCAGTCAGTCAGGCTGGGCAGTGGA TCTTGTCAATGGATTCTGCCCTGCTGTCCACCGTGTCAATGCAGTCAGTCAGGCTGGGCAGTGGA A G RF00017-4498 RNACentral:URS000099B61A SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878881855 Functional Loss SNV dbSNP153 33..33 33 - - - 40450 RMVar_ID_40450 Human_SNP_ID_715957669 A-to-I Human chrX - 46725754 46725754 46725754 GGCTCCACTGCCCAGCCTGACTGACTGCATTGACATGGTGGACAGCAGGGCAGAATCCATTGACA GGCTCCACTGCCCAGCCTGACTGACTGCATTGGCATGGTGGACAGCAGGGCAGAATCCATTGACA T C AL512633.1,SLC9A7 Ensembl:ENSG00000215284,Ensembl:ENSG00000065923 Pseudogene,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879225261 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1854555,Human_miRNA_ID_1865328,Human_miRNA_ID_1904911,Human_miRNA_ID_1907381,Human_miRNA_ID_1910134 RMVar_hsa_circ_86529,RMVar_hsa_circ_262224 40451 RMVar_ID_40451 Human_SNP_ID_715962503 A-to-I Human chrX - 46755574 46755574 46755574 CACCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCACCCGGCTGTAATAG CACCCACCTCAGCCTCCCAAAGTGCTGGGATTGCAGGTGTGAGCCACCGCACCCGGCTGTAATAG T C SLC9A7 Ensembl:ENSG00000065923 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs782794209 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86529,RMVar_hsa_circ_262224 40452 RMVar_ID_40452 Human_SNP_ID_715984478 A-to-I Human chrX - 46885461 46885461 46885461 TTGTCCAGGCCGGTCTCGAATTCCTGACCTCAAGTGATCCTCCAACCTTGGCCTCCCAAAGTACT TTGTCCAGGCCGGTCTCGAATTCCTGACCTCAGGTGATCCTCCAACCTTGGCCTCCCAAAGTACT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1245839253 Functional Loss SNV dbSNP153 33..33 33 - - - 40453 RMVar_ID_40453 Human_SNP_ID_716026663 A-to-I Human chrX + 47136115 47136115 47136115 AGAAGGCAGAGGTTGCAGTGAGCCAAGATCGCACCACTGTACTCCAGCTGGGATGACAGAGTGAG AGAAGGCAGAGGTTGCAGTGAGCCAAGATCGCGCCACTGTACTCCAGCTGGGATGACAGAGTGAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1189869856 Functional Loss SNV dbSNP153 33..33 33 - - - 40454 RMVar_ID_40454 Human_SNP_ID_716027748 A-to-I Human chrX - 47142597 47142597 47142597 ATCTGCCTGACTACAGGTGCACAGGGTGTCCAAGAGCGTGGGATGGGTAAGAGGCAGAGGCAGGG ATCTGCCTGACTACAGGTGCACAGGGTGTCCAGGAGCGTGGGATGGGTAAGAGGCAGAGGCAGGG T C NDUFB11 Ensembl:ENSG00000147123 Protein coding intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs782722665 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_735087,Human_RBP_ID_17666957,Human_RBP_ID_19149077 Human_Splice_Rec_2200930 RMVar_hsa_circ_83442,RMVar_hsa_circ_106217,RMVar_hsa_circ_262235,RMVar_hsa_circ_262236 40455 RMVar_ID_40455 Human_SNP_ID_716028137 A-to-I Human chrX - 47144586 47144586 47144586 GGCTCCCGGCCGCCCGCGTCCGCTGGGAATCTAGCTTCTCCAGGACTGTGGTCGCCCCGTCCGCT GGCTCCCGGCCGCCCGCGTCCGCTGGGAATCTGGCTTCTCCAGGACTGTGGTCGCCCCGTCCGCT T C NDUFB11 Ensembl:ENSG00000147123 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) 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 40456 RMVar_ID_40456 Human_SNP_ID_716029310 A-to-I Human chrX + 47151228 47151228 47151228 GCCCAGCTAATTTTTTGTAGAGACGGAGTTTCACCATGTTGTCCAGGCTGATCTTGAACTCCTGA GCCCAGCTAATTTTTTGTAGAGACGGAGTTTCGCCATGTTGTCCAGGCTGATCTTGAACTCCTGA A G RBM10 Ensembl:ENSG00000182872 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs782572648 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16896122 RMVar_hsa_circ_7245 40457 RMVar_ID_40457 Human_SNP_ID_716029311 A-to-I Human chrX + 47151228 47151228 47151228 GCCCAGCTAATTTTTTGTAGAGACGGAGTTTCACCATGTTGTCCAGGCTGATCTTGAACTCCTGA GCCCAGCTAATTTTTTGTAGAGACGGAGTTTCTCCATGTTGTCCAGGCTGATCTTGAACTCCTGA A T RBM10 Ensembl:ENSG00000182872 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs782572648 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16896122 RMVar_hsa_circ_7245 40458 RMVar_ID_40458 Human_SNP_ID_716029315 A-to-I Human chrX + 47151240 47151240 47151240 TTTTGTAGAGACGGAGTTTCACCATGTTGTCCAGGCTGATCTTGAACTCCTGAGCTCCAGCAATC TTTTGTAGAGACGGAGTTTCACCATGTTGTCCGGGCTGATCTTGAACTCCTGAGCTCCAGCAATC A G RBM10 Ensembl:ENSG00000182872 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355279594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16896122 RMVar_hsa_circ_7245 40459 RMVar_ID_40459 Human_SNP_ID_716029412 A-to-I Human chrX + 47152002 47152002 47152002 GGGAGGCCAAGGTGGTTGGATCGCTTGAGGCCAGGAGTTCAAGACCAGCCTGGCCAACATGGTGA GGGAGGCCAAGGTGGTTGGATCGCTTGAGGCCGGGAGTTCAAGACCAGCCTGGCCAACATGGTGA A G RBM10 Ensembl:ENSG00000182872 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1261522333 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7245 40460 RMVar_ID_40460 Human_SNP_ID_716030747 A-to-I Human chrX + 47159298 47159298 47159298 AGGCGTGGTGGCACGTGCCTGTAATCACAGCTACTCGGGAGGCTGAGGCAGGAGAATCTCTTGAA AGGCGTGGTGGCACGTGCCTGTAATCACAGCTTCTCGGGAGGCTGAGGCAGGAGAATCTCTTGAA A T RBM10 Ensembl:ENSG00000182872 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459294289 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7245 40461 RMVar_ID_40461 Human_SNP_ID_716031734 A-to-I Human chrX + 47164477 47164477 47164477 CTGGGAGGCAGAGGTTGCAGTGAGCTGAGATCATGCCACTGCCCTCCAGCCTGGGTGACAGAGTT CTGGGAGGCAGAGGTTGCAGTGAGCTGAGATCGTGCCACTGCCCTCCAGCCTGGGTGACAGAGTT A G RBM10 Ensembl:ENSG00000182872 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs911971940 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7245 40462 RMVar_ID_40462 Human_SNP_ID_716032002 A-to-I Human chrX + 47165897 47165897 47165897 CAAAAATTATCCGGGCGTGGCTGCGTGCATCTATAGTCCTAACTACTCGGGAGACTGAGGCAGGA CAAAAATTATCCGGGCGTGGCTGCGTGCATCTGTAGTCCTAACTACTCGGGAGACTGAGGCAGGA A G RBM10 Ensembl:ENSG00000182872 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1292373264 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7245 40463 RMVar_ID_40463 Human_SNP_ID_716039559 A-to-I Human chrX + 47205715 47205715 47205715 GTCTCTACCAAAAATACAAAAATTAGCCACGCATGGTGGCACACACCTGTGGTCCCAGCTACTCG GTCTCTACCAAAAATACAAAAATTAGCCACGCGTGGTGGCACACACCTGTGGTCCCAGCTACTCG A G UBA1,INE1 Ensembl:ENSG00000130985,Ensembl:ENSG00000224975 Protein coding,lincRNA intron,exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1474703272 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20668,RMVar_hsa_circ_89143,RMVar_hsa_circ_262252,RMVar_hsa_circ_349565,RMVar_hsa_circ_64133,RMVar_hsa_circ_28136,RMVar_hsa_circ_38306,RMVar_hsa_circ_118943,RMVar_hsa_circ_262257,RMVar_hsa_circ_112907,RMVar_hsa_circ_127422,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_122061,RMVar_hsa_circ_105010,RMVar_hsa_circ_262275,RMVar_hsa_circ_94603,RMVar_hsa_circ_262276,RMVar_hsa_circ_262277 40464 RMVar_ID_40464 Human_SNP_ID_716040289 A-to-I Human chrX + 47208835 47208835 47208835 TTTTTAGGCTGGGCATGGCGGCTGACACCTATAATCTCAGCACTCAGGAGGCCAAGGAGTGAGGT TTTTTAGGCTGGGCATGGCGGCTGACACCTATCATCTCAGCACTCAGGAGGCCAAGGAGTGAGGT A C UBA1 Ensembl:ENSG00000130985 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs781901458 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_257414,Human_RBP_ID_799575,Human_RBP_ID_848756,Human_RBP_ID_24343158 RMVar_hsa_circ_20668,RMVar_hsa_circ_89143,RMVar_hsa_circ_262252,RMVar_hsa_circ_349565,RMVar_hsa_circ_64133,RMVar_hsa_circ_118943,RMVar_hsa_circ_262257,RMVar_hsa_circ_112907,RMVar_hsa_circ_127422,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_93186,RMVar_hsa_circ_100436,RMVar_hsa_circ_262266,RMVar_hsa_circ_370331,RMVar_hsa_circ_262267,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_113628,RMVar_hsa_circ_262278,RMVar_hsa_circ_262279 40465 RMVar_ID_40465 Human_SNP_ID_716040296 A-to-I Human chrX + 47208880 47208880 47208880 AGGAGGCCAAGGAGTGAGGTTTGTTTGAGCCCAGGAGTTCAAGACCAGCCTAGGCAACATAGCAA AGGAGGCCAAGGAGTGAGGTTTGTTTGAGCCCCGGAGTTCAAGACCAGCCTAGGCAACATAGCAA A C UBA1 Ensembl:ENSG00000130985 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs999814450 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20668,RMVar_hsa_circ_89143,RMVar_hsa_circ_262252,RMVar_hsa_circ_349565,RMVar_hsa_circ_64133,RMVar_hsa_circ_118943,RMVar_hsa_circ_262257,RMVar_hsa_circ_112907,RMVar_hsa_circ_127422,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_93186,RMVar_hsa_circ_100436,RMVar_hsa_circ_262266,RMVar_hsa_circ_370331,RMVar_hsa_circ_262267,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_113628,RMVar_hsa_circ_262278,RMVar_hsa_circ_262279 40466 RMVar_ID_40466 Human_SNP_ID_716040300 A-to-I Human chrX + 47208888 47208888 47208888 AAGGAGTGAGGTTTGTTTGAGCCCAGGAGTTCAAGACCAGCCTAGGCAACATAGCAAGACCCTGT AAGGAGTGAGGTTTGTTTGAGCCCAGGAGTTCCAGACCAGCCTAGGCAACATAGCAAGACCCTGT A C UBA1 Ensembl:ENSG00000130985 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1466128792 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16897162 RMVar_hsa_circ_20668,RMVar_hsa_circ_89143,RMVar_hsa_circ_262252,RMVar_hsa_circ_349565,RMVar_hsa_circ_64133,RMVar_hsa_circ_118943,RMVar_hsa_circ_262257,RMVar_hsa_circ_112907,RMVar_hsa_circ_127422,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_93186,RMVar_hsa_circ_100436,RMVar_hsa_circ_262266,RMVar_hsa_circ_370331,RMVar_hsa_circ_262267,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_113628,RMVar_hsa_circ_262278,RMVar_hsa_circ_262279 40467 RMVar_ID_40467 Human_SNP_ID_716040302 A-to-I Human chrX + 47208899 47208899 47208899 TTTGTTTGAGCCCAGGAGTTCAAGACCAGCCTAGGCAACATAGCAAGACCCTGTCTCTACAACAA TTTGTTTGAGCCCAGGAGTTCAAGACCAGCCTCGGCAACATAGCAAGACCCTGTCTCTACAACAA A C UBA1 Ensembl:ENSG00000130985 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs955527646 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16897162 RMVar_hsa_circ_20668,RMVar_hsa_circ_89143,RMVar_hsa_circ_262252,RMVar_hsa_circ_349565,RMVar_hsa_circ_64133,RMVar_hsa_circ_118943,RMVar_hsa_circ_262257,RMVar_hsa_circ_112907,RMVar_hsa_circ_127422,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_93186,RMVar_hsa_circ_100436,RMVar_hsa_circ_262266,RMVar_hsa_circ_370331,RMVar_hsa_circ_262267,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_113628,RMVar_hsa_circ_262278,RMVar_hsa_circ_262279 40468 RMVar_ID_40468 Human_SNP_ID_716040355 A-to-I Human chrX + 47209178 47209177 47209179 AAATCAACTTCATTGATTTTTCTTTTTTTGAGACAGTCTTCCTCTGTCACCCAGGCTGGAGTGCA AAATCAACTTCATTGATTTTTCTTTTTTTGAG__AGTCTTCCTCTGTCACCCAGGCTGGAGTGCA GAC G UBA1 Ensembl:ENSG00000130985 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1556792478 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_24343162,Human_RBP_ID_26280731 RMVar_hsa_circ_20668,RMVar_hsa_circ_89143,RMVar_hsa_circ_262252,RMVar_hsa_circ_349565,RMVar_hsa_circ_64133,RMVar_hsa_circ_118943,RMVar_hsa_circ_262257,RMVar_hsa_circ_112907,RMVar_hsa_circ_127422,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_93186,RMVar_hsa_circ_100436,RMVar_hsa_circ_262266,RMVar_hsa_circ_370331,RMVar_hsa_circ_262267,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_113628,RMVar_hsa_circ_262278,RMVar_hsa_circ_262279 40469 RMVar_ID_40469 Human_SNP_ID_716040377 A-to-I Human chrX + 47209315 47209315 47209315 AGCTGGGATTACAGGCATCTGCCACCACGCCCAGCTACTTTTTGTATTTTTAGTAGAGATGGGGT AGCTGGGATTACAGGCATCTGCCACCACGCCCGGCTACTTTTTGTATTTTTAGTAGAGATGGGGT A G UBA1 Ensembl:ENSG00000130985 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs903892087 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20668,RMVar_hsa_circ_89143,RMVar_hsa_circ_262252,RMVar_hsa_circ_349565,RMVar_hsa_circ_64133,RMVar_hsa_circ_118943,RMVar_hsa_circ_262257,RMVar_hsa_circ_112907,RMVar_hsa_circ_127422,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_93186,RMVar_hsa_circ_100436,RMVar_hsa_circ_262266,RMVar_hsa_circ_370331,RMVar_hsa_circ_262267,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_113628,RMVar_hsa_circ_262278,RMVar_hsa_circ_262279 40470 RMVar_ID_40470 Human_SNP_ID_716087042 A-to-I Human chrX - 47452752 47452752 47452752 CCCCGTCTCTACTAAAAATACAAAAATTAGCTAGGTGTGGTGGCCCACGCCTGTAATCCAGTTAC CCCCGTCTCTACTAAAAATACAAAAATTAGCTGGGTGTGGTGGCCCACGCCTGTAATCCAGTTAC T C ZNF41 Ensembl:ENSG00000147124 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs778529077 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_262319 40471 RMVar_ID_40471 Human_SNP_ID_716123101 A-to-I Human chrX - 47656269 47656269 47656269 GTGACTGTTTACAGCTGCGATCATAGCATACTACATCCTCAAACTCCTGGGCTCAAGCAATCCCC GTGACTGTTTACAGCTGCGATCATAGCATACTGCATCCTCAAACTCCTGGGCTCAAGCAATCCCC T C UXT Ensembl:ENSG00000126756 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1445266645 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75664,RMVar_hsa_circ_115002,RMVar_hsa_circ_262334,RMVar_hsa_circ_262335 40472 RMVar_ID_40472 Human_SNP_ID_716148739 A-to-I Human chrX + 47804602 47804591 47804603 CAAGTCCTCCTTGCCTGCCATAAGCGATGCCCATAGCGACCTGCTTTCAGCCATCTGTCAAGGTT CAAGTCCTCCTTGCCTGCCATA____________AGCGACCTGCTTTCAGCCATCTGTCAAGGTT AAGCGATGCCCAT A WASF4P Ensembl:ENSG00000188459 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs782271477 Functional Loss DEL dbSNP153 23..34 33 - - - 40473 RMVar_ID_40473 Human_SNP_ID_716148745 A-to-I Human chrX + 47804602 47804602 47804602 CAAGTCCTCCTTGCCTGCCATAAGCGATGCCCATAGCGACCTGCTTTCAGCCATCTGTCAAGGTT CAAGTCCTCCTTGCCTGCCATAAGCGATGCCCGTAGCGACCTGCTTTCAGCCATCTGTCAAGGTT A G WASF4P Ensembl:ENSG00000188459 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1418928152 Functional Loss SNV dbSNP153 33..33 33 - - - 40474 RMVar_ID_40474 Human_SNP_ID_716148766 A-to-I Human chrX + 47804662 47804662 47804662 AGGTTTTCAGCTGCGCAGGGTTGAGGAGCAGCAGGAACAAGAGAAGTGGGATGTCGTGGGCAATG AGGTTTTCAGCTGCGCAGGGTTGAGGAGCAGCGGGAACAAGAGAAGTGGGATGTCGTGGGCAATG A G WASF4P Ensembl:ENSG00000188459 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1380879361 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21874041 Human_miRNA_ID_1912453 40475 RMVar_ID_40475 Human_SNP_ID_716241076 A-to-I Human chrX - 48296477 48296477 48296477 CACGCCCGGGTAATTTTTTTTGTGTTTTTGGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGG CACGCCCGGGTAATTTTTTTTGTGTTTTTGGTCGAGACGGGGTTTCACCGTGTTAGCCAGGATGG T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1206910243 Functional Loss SNV dbSNP153 33..33 33 - - - 40476 RMVar_ID_40476 Human_SNP_ID_716265364 A-to-I Human chrX - 48448118 48448118 48448118 CACAAAGTTCTTCCTATGAATACAGGAATGGAAGCTGGAGAGACTGCCTGTAAACTAGCTCATAA CACAAAGTTCTTCCTATGAATACAGGAATGGAGGCTGGAGAGACTGCCTGTAAACTAGCTCATAA T C AL606490.2 Ensembl:ENSG00000226971 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879997879 Functional Loss SNV dbSNP153 33..33 33 - - - 40477 RMVar_ID_40477 Human_SNP_ID_716265365 A-to-I Human chrX - 48448123 48448123 48448123 ACTACCACAAAGTTCTTCCTATGAATACAGGAATGGAAGCTGGAGAGACTGCCTGTAAACTAGCT ACTACCACAAAGTTCTTCCTATGAATACAGGAGTGGAAGCTGGAGAGACTGCCTGTAAACTAGCT T C AL606490.2 Ensembl:ENSG00000226971 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879987483 Functional Loss SNV dbSNP153 33..33 33 - - - 40478 RMVar_ID_40478 Human_SNP_ID_716272013 A-to-I Human chrX + 48484187 48484187 48484187 CATCTACCAAGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAATAGCTGGGATTACAGTGCCCGC CATCTACCAAGTTCAAGCGATTCTCCTGCCTCGGCCTCCCAAATAGCTGGGATTACAGTGCCCGC A G FTSJ1 Ensembl:ENSG00000068438 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1452599362 Functional Loss SNV dbSNP153 33..33 33 - - - 40479 RMVar_ID_40479 Human_SNP_ID_716278470 A-to-I Human chrX + 48522696 48522695 48522697 TTTTTCTTTTCTTTTTTATTTTATTTTGAGACAGAGTCTCGCTCTGTTGCCCAGGCTGGAGTGCA TTTTTCTTTTCTTTTTTATTTTATTTTGAGAC__AGTCTCGCTCTGTTGCCCAGGCTGGAGTGCA CAG C AF196969.1,EBP Ensembl:ENSG00000286268,Ensembl:ENSG00000147155 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1437222327 Functional Loss DEL dbSNP153 33..34 33 - - - 40480 RMVar_ID_40480 Human_SNP_ID_716278510 A-to-I Human chrX + 48522916 48522916 48522916 GCTGGTCTTGAACTCCTGAGCTCAAGTGGTCCACTCGTCTTGGCCTCCCAAAGTGCTGGGATTAC GCTGGTCTTGAACTCCTGAGCTCAAGTGGTCCCCTCGTCTTGGCCTCCCAAAGTGCTGGGATTAC A C AF196969.1,EBP Ensembl:ENSG00000286268,Ensembl:ENSG00000147155 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1556976814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8719636 40481 RMVar_ID_40481 Human_SNP_ID_716278537 A-to-I Human chrX + 48523111 48523097 48523111 TACTAGCTGGGACTACAGGCCTTTGTCACCACACCTGACTGATTTTCTTATTTTTTTAGAGACAG TACTAGCTGGGACTACAGG______________CCTGACTGATTTTCTTATTTTTTTAGAGACAG GCCTTTGTCACCACA G AF196969.1,EBP Ensembl:ENSG00000286268,Ensembl:ENSG00000147155 Protein coding,Protein coding intron,intron GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 29129909,30559470 RNA-Seq:(High) rs782080670 Functional Loss DEL dbSNP153 20..33 33 - - - Human_RBP_ID_8006471,Human_RBP_ID_16898658 40482 RMVar_ID_40482 Human_SNP_ID_716278558 A-to-I Human chrX + 48523185 48523185 48523185 GTTGCCCAGGCCGGACTTGAATTCCTGGCCTCAGGTGCTGCTCCTGCATCAGCCTCCCAAAGCAC GTTGCCCAGGCCGGACTTGAATTCCTGGCCTCGGGTGCTGCTCCTGCATCAGCCTCCCAAAGCAC A G AF196969.1,EBP Ensembl:ENSG00000286268,Ensembl:ENSG00000147155 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1224241893 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5135906,Human_RBP_ID_17579906,Human_RBP_ID_22484929 40483 RMVar_ID_40483 Human_SNP_ID_716278578 A-to-I Human chrX + 48523283 48523282 48523283 CATGGTCTTAAAACAGAATGTAGGCCGGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGG CATGGTCTTAAAACAGAATGTAGGCCGGGCGC_GTGGCTCACGCCTGTAATCCCAGCACTTTGGG CA C AF196969.1,EBP Ensembl:ENSG00000286268,Ensembl:ENSG00000147155 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1201979227 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_16898667 40484 RMVar_ID_40484 Human_SNP_ID_716278580 A-to-I Human chrX + 48523283 48523283 48523283 CATGGTCTTAAAACAGAATGTAGGCCGGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGG CATGGTCTTAAAACAGAATGTAGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG A G AF196969.1,EBP Ensembl:ENSG00000286268,Ensembl:ENSG00000147155 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1479644982 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16898667 40485 RMVar_ID_40485 Human_SNP_ID_716278921 A-to-I Human chrX + 48524806 48524806 48524806 CAACTCCTGGGTTCAAGCGATCGTCTTGCCTCAGCCTCCCCAGTAGCTGGGACTATACTATAGGT CAACTCCTGGGTTCAAGCGATCGTCTTGCCTCGGCCTCCCCAGTAGCTGGGACTATACTATAGGT A G AF196969.1,AF196972.2,EBP Ensembl:ENSG00000286268,Ensembl:ENSG00000276823,Ensembl:ENSG00000147155 Protein coding,Other,Protein coding intron,exon,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1315061917 Functional Loss SNV dbSNP153 33..33 33 - - - 40486 RMVar_ID_40486 Human_SNP_ID_716282178 A-to-I Human chrX + 48543812 48543812 48543812 AGGCTGAGGCAGGAGAATGGCATGGGCCCGGGAGGCGGAGCTTGCAGCGAGCCGAGATCGCACCA AGGCTGAGGCAGGAGAATGGCATGGGCCCGGGGGGCGGAGCTTGCAGCGAGCCGAGATCGCACCA A G AF196969.1,TBC1D25 Ensembl:ENSG00000286268,Ensembl:ENSG00000068354 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1387894309 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_262364,RMVar_hsa_circ_333020 40487 RMVar_ID_40487 Human_SNP_ID_716283013 A-to-I Human chrX + 48548368 48548368 48548368 GAACTCCTGGACTCAAGCAGTCTGCCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAAGCAAGAG GAACTCCTGGACTCAAGCAGTCTGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAAGCAAGAG A G TBC1D25 Ensembl:ENSG00000068354 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1446547463 Functional Loss SNV dbSNP153 33..33 33 - - - 40488 RMVar_ID_40488 Human_SNP_ID_716288836 A-to-I Human chrX + 48577942 48577942 48577942 ATCTGTACTAAACATAAAAAAATTAGCCTGGCATGGTGGTGTACGCCTGTAATCCCAGTGACTTG ATCTGTACTAAACATAAAAAAATTAGCCTGGCGTGGTGGTGTACGCCTGTAATCCCAGTGACTTG A G RBM3 Ensembl:ENSG00000102317 Protein coding 3'UTR GSE100210;GSE107867 HepG2 cell line;ASD brains,temporal_cortex - 29129909,30559470 RNA-Seq:(High) rs1217962244 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_735582,Human_RBP_ID_2075254,Human_RBP_ID_5231188,Human_RBP_ID_16898996,Human_RBP_ID_17441611,Human_RBP_ID_18151547,Human_RBP_ID_26571840 RMVar_hsa_circ_85851,RMVar_hsa_circ_262371 40489 RMVar_ID_40489 Human_SNP_ID_716288862 A-to-I Human chrX + 48578030 48578030 48578030 TTGAACCCGGGAGGCGGAGGTTGCAGTGAGCTAAGATCGCGCCACTGTACTCCAGCCTGGGCAAC TTGAACCCGGGAGGCGGAGGTTGCAGTGAGCTGAGATCGCGCCACTGTACTCCAGCCTGGGCAAC A G RBM3 Ensembl:ENSG00000102317 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1262618892 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_735591,Human_RBP_ID_5082783,Human_RBP_ID_16898999,Human_RBP_ID_26306008,Human_RBP_ID_26571841 RMVar_hsa_circ_85851,RMVar_hsa_circ_262371 40490 RMVar_ID_40490 Human_SNP_ID_716288938 A-to-I Human chrX + 48578358 48578358 48578358 AAAAGTGGGGGCAGAGGTGGGCGGATCACCTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACAG AAAAGTGGGGGCAGAGGTGGGCGGATCACCTGCGGTCAGGAGTTCGAGACCAGCCTGGCCAACAG A C RBM3 Ensembl:ENSG00000102317 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs782467280 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8006645,Human_RBP_ID_8938651 RMVar_hsa_circ_85851,RMVar_hsa_circ_262371 40491 RMVar_ID_40491 Human_SNP_ID_716288951 A-to-I Human chrX + 48578426 48578426 48578426 AAAACCCCATCTCTACTAAAAATACAAAAGTTAGCGGGGCGTGGTGGCGGGTGCATGTAATCCCA AAAACCCCATCTCTACTAAAAATACAAAAGTTTGCGGGGCGTGGTGGCGGGTGCATGTAATCCCA A T RBM3 Ensembl:ENSG00000102317 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1450800566 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26571863 RMVar_hsa_circ_85851,RMVar_hsa_circ_262371 40492 RMVar_ID_40492 Human_SNP_ID_716289335 A-to-I Human chrX + 48580428 48580424 48580428 TTTTTTGTTGGTTTTTTTCCAGACAGGGTCTCACTCTGTCTCCCAGGCTGGAGTGCAGTGGCACA TTTTTTGTTGGTTTTTTTCCAGACAGGGT____CTCTGTCTCCCAGGCTGGAGTGCAGTGGCACA TCTCA T RBM3 Ensembl:ENSG00000102317 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1556990212 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_735633,Human_RBP_ID_17326452,Human_RBP_ID_17554696 RMVar_hsa_circ_85851,RMVar_hsa_circ_262371 40493 RMVar_ID_40493 Human_SNP_ID_716289380 A-to-I Human chrX + 48580583 48580582 48580584 CACGCCCGGCTAATTTTTGTATTAATAGAGACAGGGTTTCACCGTGTTGGGCAGGCTGGTCCTGA CACGCCCGGCTAATTTTTGTATTAATAGAGAC__GGTTTCACCGTGTTGGGCAGGCTGGTCCTGA CAG C RBM3 Ensembl:ENSG00000102317 Protein coding 3'UTR GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs1434661126 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_8006701,Human_RBP_ID_16899132,Human_RBP_ID_18151585,Human_RBP_ID_26571878 Human_miRNA_ID_1951162,Human_miRNA_ID_1952451,Human_miRNA_ID_2444712 RMVar_hsa_circ_85851,RMVar_hsa_circ_262371 40494 RMVar_ID_40494 Human_SNP_ID_716289398 A-to-I Human chrX + 48580668 48580668 48580668 CACCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCACACCTGGCCTAGGAGT CACCCGCCTCGGCCTCCCAAAGTGCTGGGATTGCAGGCGTGAGCCACCACACCTGGCCTAGGAGT A G RBM3 Ensembl:ENSG00000102317 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1389706630 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85851,RMVar_hsa_circ_262371 40495 RMVar_ID_40495 Human_SNP_ID_716289402 A-to-I Human chrX + 48580686 48580686 48580686 AAAGTGCTGGGATTACAGGCGTGAGCCACCACACCTGGCCTAGGAGTTAAGAGTATTAAATGTTA AAAGTGCTGGGATTACAGGCGTGAGCCACCACGCCTGGCCTAGGAGTTAAGAGTATTAAATGTTA A G RBM3 Ensembl:ENSG00000102317 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1058097 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_735635,Human_RBP_ID_3258298,Human_RBP_ID_16899137,Human_RBP_ID_18151586,Human_RBP_ID_23203227,Human_RBP_ID_27793797 RMVar_hsa_circ_85851,RMVar_hsa_circ_262371 40496 RMVar_ID_40496 Human_SNP_ID_716289403 A-to-I Human chrX + 48580686 48580686 48580686 AAAGTGCTGGGATTACAGGCGTGAGCCACCACACCTGGCCTAGGAGTTAAGAGTATTAAATGTTA AAAGTGCTGGGATTACAGGCGTGAGCCACCACTCCTGGCCTAGGAGTTAAGAGTATTAAATGTTA A T RBM3 Ensembl:ENSG00000102317 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1058097 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_735635,Human_RBP_ID_3258298,Human_RBP_ID_16899137,Human_RBP_ID_18151586,Human_RBP_ID_23203227,Human_RBP_ID_27793797 RMVar_hsa_circ_85851,RMVar_hsa_circ_262371 40497 RMVar_ID_40497 Human_SNP_ID_716310669 A-to-I Human chrX + 48689739 48689739 48689739 ATCAGCTGGCCGGCGCGGTGGCTCATGCCTGTAATCCAGGAACTTTGGGAGGCTAAGGCAGGAGG ATCAGCTGGCCGGCGCGGTGGCTCATGCCTGTGATCCAGGAACTTTGGGAGGCTAAGGCAGGAGG A G WAS Ensembl:ENSG00000015285 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1366705887 Functional Loss SNV dbSNP153 33..33 33 - - - 40498 RMVar_ID_40498 Human_SNP_ID_716335943 A-to-I Human chrX - 48831227 48831227 48831227 GCACTGCCCGGATCCCGTGCACCCTGGGACCCAGAAGTGCCCCCGCCATCCCGCCACCAGGACTG GCACTGCCCGGATCCCGTGCACCCTGGGACCCGGAAGTGCCCCCGCCATCCCGCCACCAGGACTG T C PCSK1N Ensembl:ENSG00000102109 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs782711131 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_735723,Human_RBP_ID_17667262,Human_RBP_ID_18963946 40499 RMVar_ID_40499 Human_SNP_ID_716336128 A-to-I Human chrX - 48831907 48831907 48831907 GACGGCCCCGCGGGCCCGGATGCTGAGGAGGCAGGCGACGAGACACCCGACGTGGACCCCGAGCT GACGGCCCCGCGGGCCCGGATGCTGAGGAGGCGGGCGACGAGACACCCGACGTGGACCCCGAGCT T C PCSK1N Ensembl:ENSG00000102109 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1557033458 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_735730,Human_RBP_ID_22778145 Human_Splice_Rec_2204380 40500 RMVar_ID_40500 Human_SNP_ID_716348467 A-to-I Human chrX + 48899348 48899348 48899348 GTGGCGGCTCAAGCTGGCATTCCCAGCACTTTAGGAGGCTGAGGCGGGTAGATTGCTTGAGTTTA GTGGCGGCTCAAGCTGGCATTCCCAGCACTTTGGGAGGCTGAGGCGGGTAGATTGCTTGAGTTTA A G PQBP1 Ensembl:ENSG00000102103 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1309163017 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9983,RMVar_hsa_circ_297508,RMVar_hsa_circ_21767 40501 RMVar_ID_40501 Human_SNP_ID_716348479 A-to-I Human chrX + 48899435 48899435 48899435 CAACATGGCAAAACCCCGTCTTTACAAAAAATACAAAAATTAATCGTGTGTTGTGGTGCATGCCT CAACATGGCAAAACCCCGTCTTTACAAAAAATGCAAAAATTAATCGTGTGTTGTGGTGCATGCCT A G PQBP1 Ensembl:ENSG00000102103 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1173530557 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9983,RMVar_hsa_circ_297508,RMVar_hsa_circ_21767 40502 RMVar_ID_40502 Human_SNP_ID_716348480 A-to-I Human chrX + 48899435 48899435 48899435 CAACATGGCAAAACCCCGTCTTTACAAAAAATACAAAAATTAATCGTGTGTTGTGGTGCATGCCT CAACATGGCAAAACCCCGTCTTTACAAAAAATTCAAAAATTAATCGTGTGTTGTGGTGCATGCCT A T PQBP1 Ensembl:ENSG00000102103 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1173530557 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9983,RMVar_hsa_circ_297508,RMVar_hsa_circ_21767 40503 RMVar_ID_40503 Human_SNP_ID_716354147 A-to-I Human chrX - 48926488 48926488 48926488 AAGTTAGCCGGGGGTGGTGGCACTCACCTGTAATCCCAGCTACTTGGGAGGCTGAGGCTGGAGAA AAGTTAGCCGGGGGTGGTGGCACTCACCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCTGGAGAA T C OTUD5 Ensembl:ENSG00000068308 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1385698576 Functional Loss SNV dbSNP153 33..33 33 - - - 40504 RMVar_ID_40504 Human_SNP_ID_716355299 A-to-I Human chrX - 48932726 48932726 48932726 TTGCCGAGGCTGACCTTGAACTCTTGGGCTCAAGTGATCCTTGTGCCTCGGCCTCCCAAAGTGCT TTGCCGAGGCTGACCTTGAACTCTTGGGCTCAGGTGATCCTTGTGCCTCGGCCTCCCAAAGTGCT T C OTUD5 Ensembl:ENSG00000068308 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1557049101 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16900181 40505 RMVar_ID_40505 Human_SNP_ID_716356510 A-to-I Human chrX - 48939861 48939861 48939861 GCAGGCAGCTACCTGGGGAGTAGGCAGTTCTCAGATGTCTCTAAAGCAAATGGTAGGACCCTATA GCAGGCAGCTACCTGGGGAGTAGGCAGTTCTCCGATGTCTCTAAAGCAAATGGTAGGACCCTATA T G OTUD5 Ensembl:ENSG00000068308 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1291325202 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_291233 40506 RMVar_ID_40506 Human_SNP_ID_716365604 A-to-I Human chrX - 48986239 48986239 48986239 TGGCCTATCTCTGCTTTTTTTTTTTTTTGTAGACGGAGTTTCGGTCTTGTTGTCCAGGCTGGAGT TGGCCTATCTCTGCTTTTTTTTTTTTTTGTAGGCGGAGTTTCGGTCTTGTTGTCCAGGCTGGAGT T C GRIPAP1 Ensembl:ENSG00000068400 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1449005806 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_338502,RMVar_hsa_circ_31253,RMVar_hsa_circ_5058,RMVar_hsa_circ_68366,RMVar_hsa_circ_32937,RMVar_hsa_circ_47330 40507 RMVar_ID_40507 Human_SNP_ID_716367431 A-to-I Human chrX - 48996495 48996495 48996495 GGAAGTACAGGCATATGCCACCATGCCTGGCTAACTTTGTATTTTTAGTAGAGATGAGAGAAAAT GGAAGTACAGGCATATGCCACCATGCCTGGCTCACTTTGTATTTTTAGTAGAGATGAGAGAAAAT T G GRIPAP1 Ensembl:ENSG00000068400 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202652137 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_338502,RMVar_hsa_circ_68366,RMVar_hsa_circ_32937,RMVar_hsa_circ_262413,RMVar_hsa_circ_103359,RMVar_hsa_circ_50982 40508 RMVar_ID_40508 Human_SNP_ID_716375340 A-to-I Human chrX - 49035128 49035128 49035128 TTTTGTATTTTTAGTAGAGACAGAGTTTCACCATGTTGGCCAGGCTGGTCACGAACTCCTGACCT TTTTGTATTTTTAGTAGAGACAGAGTTTCACCGTGTTGGCCAGGCTGGTCACGAACTCCTGACCT T C TFE3 Ensembl:ENSG00000068323 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1450622571 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32265,RMVar_hsa_circ_327605,RMVar_hsa_circ_50224 40509 RMVar_ID_40509 Human_SNP_ID_716375562 A-to-I Human chrX - 49035998 49035998 49035998 CCTGGCTAATTTTTTGCATTTTTAGTAGAGACAGGGTCTCACTGTGTTGCCCAGGCTGGTCTCGA CCTGGCTAATTTTTTGCATTTTTAGTAGAGACGGGGTCTCACTGTGTTGCCCAGGCTGGTCTCGA T C TFE3 Ensembl:ENSG00000068323 Protein coding intron GSE38233;GSE99789;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29796672,31158229 RNA-Seq:(High) rs1557074676 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32265,RMVar_hsa_circ_327605,RMVar_hsa_circ_50224 40510 RMVar_ID_40510 Human_SNP_ID_716375636 A-to-I Human chrX - 49036380 49036380 49036380 TCATTGCACCCTCTGCCTCCTGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGCCGAGA TCATTGCACCCTCTGCCTCCTGGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCCAAGTAGCCGAGA T C TFE3 Ensembl:ENSG00000068323 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1263856162 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32265,RMVar_hsa_circ_327605,RMVar_hsa_circ_50224 40511 RMVar_ID_40511 Human_SNP_ID_716375697 A-to-I Human chrX - 49036542 49036542 49036542 CCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCATGCCTGGCCTAACTTGCTTTAT CCTCGGCCTCCCAAAGTGCTGGGATTACAGGCTTGAGCCACCATGCCTGGCCTAACTTGCTTTAT T A TFE3 Ensembl:ENSG00000068323 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251714703 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32265,RMVar_hsa_circ_327605,RMVar_hsa_circ_50224 40512 RMVar_ID_40512 Human_SNP_ID_716384765 A-to-I Human chrX - 49081727 49081727 49081727 CACCTGCCTCGGCCTCCCAAATTGCTGGGATTACAGGCATGCACCACCATGCCCAGCCCTTTTTT CACCTGCCTCGGCCTCCCAAATTGCTGGGATTGCAGGCATGCACCACCATGCCCAGCCCTTTTTT T C WDR45 Ensembl:ENSG00000196998 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs782796222 Functional Loss SNV dbSNP153 33..33 33 - - - 40513 RMVar_ID_40513 Human_SNP_ID_716384962 A-to-I Human chrX - 49082756 49082756 49082756 TGAGCCGAGATCGTGCCACTGCAGTCCAGCCTAGGTGACAGAGTGAGACTCCATCTTAAAAAAAA TGAGCCGAGATCGTGCCACTGCAGTCCAGCCTGGGTGACAGAGTGAGACTCCATCTTAAAAAAAA T C WDR45 Ensembl:ENSG00000196998 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1487026045 Functional Loss SNV dbSNP153 33..33 33 - - - 40514 RMVar_ID_40514 Human_SNP_ID_716385828 A-to-I Human chrX - 49087175 49087175 49087175 TTTTGTATTTTTAGTAAAGACGGGCTTTCACCATGTCGTCCAGGCTGGTCTTGAACTCCTGACCT TTTTGTATTTTTAGTAAAGACGGGCTTTCACCGTGTCGTCCAGGCTGGTCTTGAACTCCTGACCT T C WDR45 Ensembl:ENSG00000196998 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1220647806 Functional Loss SNV dbSNP153 33..33 33 - - - 40515 RMVar_ID_40515 Human_SNP_ID_716386200 A-to-I Human chrX - 49089491 49089491 49089491 ACGTAGGAGGCAGAGGCACAAGAATCGCTTGAACCCAGGAGGCTGAGGTTGTAGTGAGCTGAGAT ACGTAGGAGGCAGAGGCACAAGAATCGCTTGAGCCCAGGAGGCTGAGGTTGTAGTGAGCTGAGAT T C WDR45 Ensembl:ENSG00000196998 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1217622717 Functional Loss SNV dbSNP153 33..33 33 - - - 40516 RMVar_ID_40516 Human_SNP_ID_716386411 A-to-I Human chrX - 49090746 49090746 49090746 ATCACCTGAGGTCAGGAGTTCAACACCAGCCTAGCCAATGTGGTGAAACTCTGCCCATGTTAAAA ATCACCTGAGGTCAGGAGTTCAACACCAGCCTGGCCAATGTGGTGAAACTCTGCCCATGTTAAAA T C WDR45 Ensembl:ENSG00000196998 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs945635057 Functional Loss SNV dbSNP153 33..33 33 - - - 40517 RMVar_ID_40517 Human_SNP_ID_716386421 A-to-I Human chrX - 49090817 49090817 49090817 AAAAAAAAAAGGCCTGGATTACGGTGGCTCACACCTGTAATCCCAGCACTTTGAGAGGCCGAAGC AAAAAAAAAAGGCCTGGATTACGGTGGCTCACGCCTGTAATCCCAGCACTTTGAGAGGCCGAAGC T C WDR45 Ensembl:ENSG00000196998 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1288426438 Functional Loss SNV dbSNP153 33..33 33 - - - 40518 RMVar_ID_40518 Human_SNP_ID_716387209 A-to-I Human chrX - 49094898 49094898 49094898 TGTAATCCCAGCTACTAGGGAGGCTGGGGCCAAGCTGGTCTTGCACACCTGACCTCAGGCGATCT TGTAATCCCAGCTACTAGGGAGGCTGGGGCCACGCTGGTCTTGCACACCTGACCTCAGGCGATCT T G WDR45 Ensembl:ENSG00000196998 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1434156236 Functional Loss SNV dbSNP153 33..33 33 - - - 40519 RMVar_ID_40519 Human_SNP_ID_716388043 A-to-I Human chrX - 49099309 49099309 49099309 CTCTGGATTTTTTTTTTTTGAAATGGAGTCTCACTCTGTTGCCATGCAGGAGTGCAGTGGTGTGA CTCTGGATTTTTTTTTTTTGAAATGGAGTCTCCCTCTGTTGCCATGCAGGAGTGCAGTGGTGTGA T G WDR45 Ensembl:ENSG00000196998 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs782394306 Functional Loss SNV dbSNP153 33..33 33 - - - 40520 RMVar_ID_40520 Human_SNP_ID_716388248 A-to-I Human chrX - 49100367 49100367 49100367 AGCCGGGCGTGGTGACGGGCGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGGATGGCG AGCCGGGCGTGGTGACGGGCGCCTGTAGTCCCGGCTACTCAGGAGGCTGAGGCAGGAGGATGGCG T C WDR45 Ensembl:ENSG00000196998 Protein coding 5'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1237257560 Functional Loss SNV dbSNP153 33..33 33 - - - 40521 RMVar_ID_40521 Human_SNP_ID_716388266 A-to-I Human chrX - 49100437 49100437 49100437 GGTCAGGAGATCGAGACCATCCTGGCTAACACAGTGAAACCCCGTCTCTACTAAAAAAATACAAA GGTCAGGAGATCGAGACCATCCTGGCTAACACGGTGAAACCCCGTCTCTACTAAAAAAATACAAA T C WDR45 Ensembl:ENSG00000196998 Protein coding 5'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs949646573 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_188836 40522 RMVar_ID_40522 Human_SNP_ID_716389056 A-to-I Human chrX - 49104696 49104696 49104696 TTGTATTTATTTTTTTAATAAGACGTGGTCTCACTCTGTCACCCAGATTGAAGTGCAGTGGCACA TTGTATTTATTTTTTTAATAAGACGTGGTCTCGCTCTGTCACCCAGATTGAAGTGCAGTGGCACA T C RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1557088664 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8007274,Human_RBP_ID_16901464 40523 RMVar_ID_40523 Human_SNP_ID_716389138 A-to-I Human chrX - 49105177 49105173 49105177 ATGTATGTATTTATTTATTTAGAGACAGTCTCACTCTGTTGCCAAGGCTGGAGTGCCATGGTGCA ATGTATGTATTTATTTATTTAGAGACAGTCTC____TGTTGCCAAGGCTGGAGTGCCATGGTGCA AGAGT A RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1282629229 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_16901476 40524 RMVar_ID_40524 Human_SNP_ID_716389190 A-to-I Human chrX - 49105423 49105423 49105423 TAGAGATGAAATTTTGCTGTGTTGCTCAGGCTAGTCTCGAACCTCTGAACTCAAGGGATCTGCCC TAGAGATGAAATTTTGCTGTGTTGCTCAGGCTCGTCTCGAACCTCTGAACTCAAGGGATCTGCCC T G RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1344374741 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16901482 40525 RMVar_ID_40525 Human_SNP_ID_716390051 A-to-I Human chrX - 49110188 49110188 49110188 TCTGTCTCCCAGGCTGATTGTGCAGGGACACAATCATGGCTCACTGCAGCCTTGATCTCCTGGGC TCTGTCTCCCAGGCTGATTGTGCAGGGACACAGTCATGGCTCACTGCAGCCTTGATCTCCTGGGC T C RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1236213467 Functional Loss SNV dbSNP153 33..33 33 - - - 40526 RMVar_ID_40526 Human_SNP_ID_716390481 A-to-I Human chrX - 49112737 49112737 49112737 TGGAGTGCAGTGGTGCAATCATAGCTCACAGCAGCATTGATCTCCTGGGCTCAAGCGATCTTCCC TGGAGTGCAGTGGTGCAATCATAGCTCACAGCGGCATTGATCTCCTGGGCTCAAGCGATCTTCCC T C RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1190853818 Functional Loss SNV dbSNP153 33..33 33 - - - 40527 RMVar_ID_40527 Human_SNP_ID_716390572 A-to-I Human chrX - 49113221 49113221 49113221 TCTTGGAATATAGATACTATAAGCTTGGGCACAGTGGTGCATGCCTGTAATCCTAGCACTTTAGG TCTTGGAATATAGATACTATAAGCTTGGGCACGGTGGTGCATGCCTGTAATCCTAGCACTTTAGG T C RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1557089619 Functional Loss SNV dbSNP153 33..33 33 - - - 40528 RMVar_ID_40528 Human_SNP_ID_716399171 A-to-I Human chrX - 49157324 49157324 49157324 TGGCCATGGAGCCGCGCACAGGGGGCGCCGCGAACCCTAAGGGGAGCAGAGGAAGTACAGGGATT TGGCCATGGAGCCGCGCACAGGGGGCGCCGCGGACCCTAAGGGGAGCAGAGGAAGTACAGGGATT T C AC231657.2 Ensembl:ENSG00000280116 Pseudogene exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs782212180 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2205866 40529 RMVar_ID_40529 Human_SNP_ID_716403924 A-to-I Human chrX - 49181176 49181176 49181176 TTTTGTAGAGATGGGGTTTTGCCATGTTGCCCAGGGTGGTCTTGGACTCCTGGGCTCAAGCTATC TTTTGTAGAGATGGGGTTTTGCCATGTTGCCCGGGGTGGTCTTGGACTCCTGGGCTCAAGCTATC T C PRICKLE3 Ensembl:ENSG00000012211 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs782679392 Functional Loss SNV dbSNP153 33..33 33 - - - 40530 RMVar_ID_40530 Human_SNP_ID_716403941 A-to-I Human chrX - 49181321 49181321 49181321 CTCTGTCTCCCAGGTTTGAGTGCAGTGGCTCAATCACAGCTCACTGCAGCCTCAACTTCCTGAGC CTCTGTCTCCCAGGTTTGAGTGCAGTGGCTCACTCACAGCTCACTGCAGCCTCAACTTCCTGAGC T G PRICKLE3 Ensembl:ENSG00000012211 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1057352817 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17579915 40531 RMVar_ID_40531 Human_SNP_ID_716404367 A-to-I Human chrX - 49182085 49182085 49182085 AAAATTAGTCTGGCATGGTGGCAAATGTCTGTAATCCCAGCTACTCGGGAGGCTGAGCCACAAGA AAAATTAGTCTGGCATGGTGGCAAATGTCTGTGATCCCAGCTACTCGGGAGGCTGAGCCACAAGA T C PRICKLE3 Ensembl:ENSG00000012211 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1381157490 Functional Loss SNV dbSNP153 33..33 33 - - - 40532 RMVar_ID_40532 Human_SNP_ID_716404550 A-to-I Human chrX - 49183105 49183105 49183105 AATAACATATCTGCCCACGGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTCGGGAGGCTGAG AATAACATATCTGCCCACGGGCACGGTGGCTCTCGCCTGTAATCCCAGCACTTCGGGAGGCTGAG T A PRICKLE3 Ensembl:ENSG00000012211 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1432854713 Functional Loss SNV dbSNP153 33..33 33 - - - 40533 RMVar_ID_40533 Human_SNP_ID_716414610 A-to-I Human chrX - 49234159 49234159 49234159 TCAAGACCAAGGATGGCATGGTGGAGATCACCAGCAAGCACGAGGAGCGGCAGGACGAGCATGGC TCAAGACCAAGGATGGCATGGTGGAGATCACCGGCAAGCACGAGGAGCGGCAGGACGAGCATGGC T C HSPB1P2 Ensembl:ENSG00000230216 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879989200 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17443379 Human_miRNA_ID_1827209 40534 RMVar_ID_40534 Human_SNP_ID_716652166 A-to-I Human chrX + 50905581 50905581 50905581 AAACCTCATCGTTACAGACCTGGTACTGTGGCACTCCGTGAAATTAGACATTATCAGAAGTCCAC AAACCTCATCGTTACAGACCTGGTACTGTGGCGCTCCGTGAAATTAGACATTATCAGAAGTCCAC A G H3P44 Ensembl:ENSG00000226881 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1433991918 Functional Loss SNV dbSNP153 33..33 33 - - - 40535 RMVar_ID_40535 Human_SNP_ID_716797019 A-to-I Human chrX - 51744604 51744604 51744604 TTTGCCAACATCGCATGTTCTCTTGTCTGTCCACCTTTTTCAAATCCAGTTTCAAACTCTCCTTT TTTGCCAACATCGCATGTTCTCTTGTCTGTCCTCCTTTTTCAAATCCAGTTTCAAACTCTCCTTT T A lnc-CENPVL2-3 RNACentral:URS0000D59CA6 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs879978767 Functional Loss SNV dbSNP153 33..33 33 - - - 40536 RMVar_ID_40536 Human_SNP_ID_716797067 A-to-I Human chrX + 51744922 51744922 51744922 AACTTCAACAGATCAATTGATGGACCAATAAGACTGCCAATTGTGGATAAGTACAAAGATATGGG AACTTCAACAGATCAATTGATGGACCAATAAGGCTGCCAATTGTGGATAAGTACAAAGATATGGG A G GSPT2 Ensembl:ENSG00000189369 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs782633997 Functional Loss SNV dbSNP153 33..33 33 - - - 40537 RMVar_ID_40537 Human_SNP_ID_716965818 A-to-I Human chrX + 52833402 52833402 52833402 AAAACAAGCATTTTGATCCATTTTGGAAAAAGATATCTTCTGTTTAACATATCAAACACTCTCCC AAAACAAGCATTTTGATCCATTTTGGAAAAAGGTATCTTCTGTTTAACATATCAAACACTCTCCC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879958417 Functional Loss SNV dbSNP153 33..33 33 - - - 40538 RMVar_ID_40538 Human_SNP_ID_717000979 A-to-I Human chrX + 53079766 53079766 53079766 TGCCTGTATATGGGGACAGATACAGCACGTGCATGCATACACACACACACACACACACCACAGTT TGCCTGTATATGGGGACAGATACAGCACGTGCGTGCATACACACACACACACACACACCACAGTT A G GPR173 Ensembl:ENSG00000184194 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1471017487 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105078,RMVar_hsa_circ_262466 40539 RMVar_ID_40539 Human_SNP_ID_717005929 A-to-I Human chrX + 53100642 53100642 53100642 CAACATAGTGAAACCCCGTCTCTACTAAAAGTACAAAAATTGGCTGGGCGTGGTGGCGGGCACCT CAACATAGTGAAACCCCGTCTCTACTAAAAGTGCAAAAATTGGCTGGGCGTGGTGGCGGGCACCT A G KANTR Ensembl:ENSG00000232593 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1430641346 Functional Loss SNV dbSNP153 33..33 33 - - - 40540 RMVar_ID_40540 Human_SNP_ID_717007999 A-to-I Human chrX + 53111290 53111290 53111290 GCAGTCCTCCTGCCTCGGCCTCCTAAAGTGCTAGGAGTACAGGCCTGAGCCACCACACCCAGCCT GCAGTCCTCCTGCCTCGGCCTCCTAAAGTGCTGGGAGTACAGGCCTGAGCCACCACACCCAGCCT A G KANTR Ensembl:ENSG00000232593 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1313479156 Functional Loss SNV dbSNP153 33..33 33 - - - 40541 RMVar_ID_40541 Human_SNP_ID_717009239 A-to-I Human chrX + 53118736 53118736 53118736 TGAGCTGAGATCACACTACTGCATTTGAGCCTAGGCGGCAGAACTAGACTCTGTCTCAAAAAAAA TGAGCTGAGATCACACTACTGCATTTGAGCCTGGGCGGCAGAACTAGACTCTGTCTCAAAAAAAA A G KANTR Ensembl:ENSG00000232593 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1483265692 Functional Loss SNV dbSNP153 33..33 33 - - - 40542 RMVar_ID_40542 Human_SNP_ID_717009423 A-to-I Human chrX + 53119879 53119879 53119879 GTAGCTGAGACTACCATCATGCCATAATGCCCAGCTAATTTTTGTATTTTTTGTAGAGACAGGGT GTAGCTGAGACTACCATCATGCCATAATGCCCTGCTAATTTTTGTATTTTTTGTAGAGACAGGGT A T KANTR Ensembl:ENSG00000232593 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs980625188 Functional Loss SNV dbSNP153 33..33 33 - - - 40543 RMVar_ID_40543 Human_SNP_ID_717011909 A-to-I Human chrX + 53136372 53136372 53136372 GCGGTTCTCCTGCCTCAGCCTCCCGAGTAGCTAGGACTACAGGTGTAAACTACCACGCCTGGCTG GCGGTTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGTGTAAACTACCACGCCTGGCTG A G KANTR Ensembl:ENSG00000232593 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1556817631 Functional Loss SNV dbSNP153 33..33 33 - - - 40544 RMVar_ID_40544 Human_SNP_ID_717029231 A-to-I Human chrX - 53233720 53233720 53233720 GCCAAACTTCAGCTGGCTTGGCCCTCTCTCTGACCTCAGGGCCTGGCCACACACTTCCATGTGTC GCCAAACTTCAGCTGGCTTGGCCCTCTCTCTGGCCTCAGGGCCTGGCCACACACTTCCATGTGTC T C IQSEC2 Ensembl:ENSG00000124313 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1434279871 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18921279 40545 RMVar_ID_40545 Human_SNP_ID_717036992 A-to-I Human chrX - 53279150 53279150 53279150 CTGAGATGGAGTCTTGCTCTGTCGCCCAGACTAGAGTGCTGTGGTGCGATCTCGGCTCACTGCAG CTGAGATGGAGTCTTGCTCTGTCGCCCAGACTGGAGTGCTGTGGTGCGATCTCGGCTCACTGCAG T C IQSEC2 Ensembl:ENSG00000124313 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1056963331 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_262485,RMVar_hsa_circ_127110 40546 RMVar_ID_40546 Human_SNP_ID_717054499 A-to-I Human chrX - 53384754 53384754 53384754 TTTTGTAGAGACGGAGTCTCCCTATTTTGCCCAGGCTGGTCTCAAATTCCTATTCTCAAGTGATT TTTTGTAGAGACGGAGTCTCCCTATTTTGCCCTGGCTGGTCTCAAATTCCTATTCTCAAGTGATT T A SMC1A Ensembl:ENSG00000072501 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1169827619 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71480 40547 RMVar_ID_40547 Human_SNP_ID_717056058 A-to-I Human chrX - 53392852 53392852 53392852 TTAGAGACAGTGGAAACAAAAACCAGAATTCAATAGATATTTAGGGCCGGGCACAGTGGCTCATG TTAGAGACAGTGGAAACAAAAACCAGAATTCAGTAGATATTTAGGGCCGGGCACAGTGGCTCATG T C SMC1A Ensembl:ENSG00000072501 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1164983707 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71480 40548 RMVar_ID_40548 Human_SNP_ID_717060649 A-to-I Human chrX - 53418633 53418633 53418633 GCTCAGGAGTTTGAGACCAGCCTAGGCAACATAGGGAGACCCTGCTTCTGCAAAAATCCAAAAAC GCTCAGGAGTTTGAGACCAGCCTAGGCAACATGGGGAGACCCTGCTTCTGCAAAAATCCAAAAAC T C SMC1A Ensembl:ENSG00000072501 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1228041862 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26283168 40549 RMVar_ID_40549 Human_SNP_ID_717060836 A-to-I Human chrX - 53419440 53419440 53419440 TCACTGCAGCCTCAACTTCTCGGGCTCAAGCAACCCTCCCATCTCAGCCTTCCCAGTAGTCAGGA TCACTGCAGCCTCAACTTCTCGGGCTCAAGCAGCCCTCCCATCTCAGCCTTCCCAGTAGTCAGGA T C SMC1A Ensembl:ENSG00000072501 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1314625048 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16905127 40550 RMVar_ID_40550 Human_SNP_ID_717083475 A-to-I Human chrX - 53541754 53541754 53541754 TCAATCGATCCTCCTGCCTTGGCTATCTGAGTAGCTGGAACTGTAAGGGACAGGCCACCATGCCC TCAATCGATCCTCCTGCCTTGGCTATCTGAGTTGCTGGAACTGTAAGGGACAGGCCACCATGCCC T A HUWE1 Ensembl:ENSG00000086758 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1556918693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16905456 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 40551 RMVar_ID_40551 Human_SNP_ID_717085715 A-to-I Human chrX - 53553337 53553337 53553337 GAATTCAAGATCAGCCTGGCCAAGATGGTGAAACCCCATCTCTACTAAAAATACAAAAAACTGGC GAATTCAAGATCAGCCTGGCCAAGATGGTGAAGCCCCATCTCTACTAAAAATACAAAAAACTGGC T C HUWE1 Ensembl:ENSG00000086758 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1228905483 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108436,RMVar_hsa_circ_127266,RMVar_hsa_circ_262502,RMVar_hsa_circ_262503,RMVar_hsa_circ_75758,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_79230,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_89256,RMVar_hsa_circ_262532,RMVar_hsa_circ_262534,RMVar_hsa_circ_262533,RMVar_hsa_circ_108327,RMVar_hsa_circ_118170,RMVar_hsa_circ_262538,RMVar_hsa_circ_262539,RMVar_hsa_circ_102446,RMVar_hsa_circ_78196,RMVar_hsa_circ_262540,RMVar_hsa_circ_127901,RMVar_hsa_circ_262542,RMVar_hsa_circ_262543 40552 RMVar_ID_40552 Human_SNP_ID_717093014 A-to-I Human chrX - 53589681 53589681 53589681 AACAAGATGAGCTCCACACTTTCACAGATACTATGTTGCCAGGCTGCTTCCACCTTCTTGATGAG AACAAGATGAGCTCCACACTTTCACAGATACTGTGTTGCCAGGCTGCTTCCACCTTCTTGATGAG T C HUWE1 Ensembl:ENSG00000086758 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs782689857 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_93177,Human_RBP_ID_220046,Human_RBP_ID_2075951,Human_RBP_ID_5068131,Human_RBP_ID_5483662,Human_RBP_ID_8936707,Human_RBP_ID_9265332,Human_RBP_ID_17326699,Human_RBP_ID_17554940,Human_RBP_ID_18921716,Human_RBP_ID_22841749,Human_RBP_ID_26362600 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_365656,RMVar_hsa_circ_262565,RMVar_hsa_circ_352912,RMVar_hsa_circ_17816,RMVar_hsa_circ_262566 40553 RMVar_ID_40553 Human_SNP_ID_717101827 A-to-I Human chrX - 53636659 53636659 53636659 GGAGTGCAGTGGTGCAATTTCAGCTCACTGCAACCTCTGCCTCCCGGGTTCAGGCCATCCTCCCA GGAGTGCAGTGGTGCAATTTCAGCTCACTGCAGCCTCTGCCTCCCGGGTTCAGGCCATCCTCCCA T C HUWE1 Ensembl:ENSG00000086758 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1473520821 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16907140 RMVar_hsa_circ_49196,RMVar_hsa_circ_40553,RMVar_hsa_circ_348017,RMVar_hsa_circ_322627,RMVar_hsa_circ_75030,RMVar_hsa_circ_61737,RMVar_hsa_circ_369246,RMVar_hsa_circ_324846,RMVar_hsa_circ_51053,RMVar_hsa_circ_338104,RMVar_hsa_circ_22480,RMVar_hsa_circ_60780,RMVar_hsa_circ_341711,RMVar_hsa_circ_25871,RMVar_hsa_circ_31367,RMVar_hsa_circ_344757,RMVar_hsa_circ_57666,RMVar_hsa_circ_332066,RMVar_hsa_circ_335287 40554 RMVar_ID_40554 Human_SNP_ID_717106641 A-to-I Human chrX - 53662844 53662844 53662844 ATCTGCCCTCAGCCTCCCAAAGTGCTAAGATTATAGGCTTGAGCCATTGTACCCGGCCCCTTCTT ATCTGCCCTCAGCCTCCCAAAGTGCTAAGATTGTAGGCTTGAGCCATTGTACCCGGCCCCTTCTT T C HUWE1 Ensembl:ENSG00000086758 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1379036640 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10466891 RMVar_hsa_circ_49196,RMVar_hsa_circ_40553,RMVar_hsa_circ_369246,RMVar_hsa_circ_22480,RMVar_hsa_circ_60780,RMVar_hsa_circ_31367,RMVar_hsa_circ_344757,RMVar_hsa_circ_275568,RMVar_hsa_circ_335287,RMVar_hsa_circ_62041 40555 RMVar_ID_40555 Human_SNP_ID_717107195 A-to-I Human chrX - 53665888 53665888 53665888 CCTCAGGCTTATCCTCCCACCTCAGGCTTCCAAAGTGCTGGGATTACAGGCATGCAGCCAGAAAC CCTCAGGCTTATCCTCCCACCTCAGGCTTCCAGAGTGCTGGGATTACAGGCATGCAGCCAGAAAC T C HUWE1 Ensembl:ENSG00000086758 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1482346766 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16908294 RMVar_hsa_circ_49196,RMVar_hsa_circ_40553,RMVar_hsa_circ_369246,RMVar_hsa_circ_22480,RMVar_hsa_circ_60780,RMVar_hsa_circ_31367,RMVar_hsa_circ_344757,RMVar_hsa_circ_275568,RMVar_hsa_circ_335287,RMVar_hsa_circ_62041 40556 RMVar_ID_40556 Human_SNP_ID_717107226 A-to-I Human chrX - 53665999 53665995 53665999 TACAGGCAGGCTTTTCTTATAAATTTTTATTTATTTTTTGTAGAGACGGAGGTCTCACTCTGTGG TACAGGCAGGCTTTTCTTATAAATTTTTATTT____TTTGTAGAGACGGAGGTCTCACTCTGTGG AAAAT A HUWE1 Ensembl:ENSG00000086758 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1557047413 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_8010093,Human_RBP_ID_16908297 RMVar_hsa_circ_49196,RMVar_hsa_circ_40553,RMVar_hsa_circ_369246,RMVar_hsa_circ_22480,RMVar_hsa_circ_60780,RMVar_hsa_circ_31367,RMVar_hsa_circ_344757,RMVar_hsa_circ_275568,RMVar_hsa_circ_335287,RMVar_hsa_circ_62041 40557 RMVar_ID_40557 Human_SNP_ID_717160224 A-to-I Human chrX - 53955370 53955370 53955370 TCGATATAGAAAACACAGGTATGGGGCTGAGCATGGTGGTTAATGCCTGTAATCCTAGCACTTTG TCGATATAGAAAACACAGGTATGGGGCTGAGCGTGGTGGTTAATGCCTGTAATCCTAGCACTTTG T C PHF8 Ensembl:ENSG00000172943 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs999086459 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8010434 RMVar_hsa_circ_92770,RMVar_hsa_circ_262580 40558 RMVar_ID_40558 Human_SNP_ID_717161520 A-to-I Human chrX - 53961468 53961468 53961468 AGAAAATCAGCCGGGAATGGTGGCGGGCGCCTATAATCCCAGCTAGTTGGGAGGCTGAGGTAGGA AGAAAATCAGCCGGGAATGGTGGCGGGCGCCTGTAATCCCAGCTAGTTGGGAGGCTGAGGTAGGA T C PHF8 Ensembl:ENSG00000172943 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1177097089 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26284971 RMVar_hsa_circ_92770,RMVar_hsa_circ_262580 40559 RMVar_ID_40559 Human_SNP_ID_717184339 A-to-I Human chrX - 54084644 54084644 54084644 TTGTATTTTTAGTAGAGACGGGGTTTTACCATATTCGTCAGGCTGGTCTTGAACTCCCATCCTCA TTGTATTTTTAGTAGAGACGGGGTTTTACCATGTTCGTCAGGCTGGTCTTGAACTCCCATCCTCA T C FAM120C Ensembl:ENSG00000184083 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1356067313 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67538,RMVar_hsa_circ_265750,RMVar_hsa_circ_29715 40560 RMVar_ID_40560 Human_SNP_ID_717197888 A-to-I Human chrX - 54164673 54164673 54164673 GTACTATTCACAGTAGCCAAGAGTTGGAAGCAACCCAAATGTCTGTTGATGGATGAATGGATAAA GTACTATTCACAGTAGCCAAGAGTTGGAAGCATCCCAAATGTCTGTTGATGGATGAATGGATAAA T A FAM120C Ensembl:ENSG00000184083 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1557134896 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107713,RMVar_hsa_circ_262598,RMVar_hsa_circ_266420 40561 RMVar_ID_40561 Human_SNP_ID_717244966 A-to-I Human chrX + 54444909 54444906 54444909 TGCCGGTGGACAGTGGGCAGGTGGATTTGGGGAGGAGAGGATCAGCAGCAGCAGCAGTACTCAGT TGCCGGTGGACAGTGGGCAGGTGGATTTGG___GGAGAGGATCAGCAGCAGCAGCAGTACTCAGT GGGA G TSR2 Ensembl:ENSG00000158526 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1243696477 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_736694,Human_RBP_ID_1062980,Human_RBP_ID_8010938,Human_RBP_ID_17667058,Human_RBP_ID_18152508,Human_RBP_ID_24347206,Human_RBP_ID_26573800 40562 RMVar_ID_40562 Human_SNP_ID_717247318 A-to-I Human chrX - 54458292 54458292 54458292 TGCCCCCCTCGGCCTCCTAAAGTATTGGGATTACAGGCATGAACCACCACGCCCAGCCTCACCAA TGCCCCCCTCGGCCTCCTAAAGTATTGGGATTTCAGGCATGAACCACCACGCCCAGCCTCACCAA T A FGD1 Ensembl:ENSG00000102302 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985819274 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95353,RMVar_hsa_circ_95448,RMVar_hsa_circ_82634,RMVar_hsa_circ_262629,RMVar_hsa_circ_85876,RMVar_hsa_circ_262630,RMVar_hsa_circ_262628,RMVar_hsa_circ_24259,RMVar_hsa_circ_262631,RMVar_hsa_circ_106665,RMVar_hsa_circ_262634,RMVar_hsa_circ_293568,RMVar_hsa_circ_262636,RMVar_hsa_circ_262637,RMVar_hsa_circ_376050 40563 RMVar_ID_40563 Human_SNP_ID_717247321 A-to-I Human chrX - 54458301 54458301 54458301 CAGGTGATCTGCCCCCCTCGGCCTCCTAAAGTATTGGGATTACAGGCATGAACCACCACGCCCAG CAGGTGATCTGCCCCCCTCGGCCTCCTAAAGTGTTGGGATTACAGGCATGAACCACCACGCCCAG T C FGD1 Ensembl:ENSG00000102302 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1478365682 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95353,RMVar_hsa_circ_95448,RMVar_hsa_circ_82634,RMVar_hsa_circ_262629,RMVar_hsa_circ_85876,RMVar_hsa_circ_262630,RMVar_hsa_circ_262628,RMVar_hsa_circ_24259,RMVar_hsa_circ_262631,RMVar_hsa_circ_106665,RMVar_hsa_circ_262634,RMVar_hsa_circ_293568,RMVar_hsa_circ_262636,RMVar_hsa_circ_262637,RMVar_hsa_circ_376050 40564 RMVar_ID_40564 Human_SNP_ID_717248136 A-to-I Human chrX - 54462889 54462889 54462889 ATGATGGTGCACGCCTGTAATTCCAGCTAGTCAGGAGGCTGAGGCAGTAGAACCACTTGAACCCG ATGATGGTGCACGCCTGTAATTCCAGCTAGTCCGGAGGCTGAGGCAGTAGAACCACTTGAACCCG T G FGD1 Ensembl:ENSG00000102302 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1218605187 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95353,RMVar_hsa_circ_95448,RMVar_hsa_circ_82634,RMVar_hsa_circ_262629,RMVar_hsa_circ_85876,RMVar_hsa_circ_262630,RMVar_hsa_circ_262628,RMVar_hsa_circ_24259,RMVar_hsa_circ_262631,RMVar_hsa_circ_106665,RMVar_hsa_circ_262634,RMVar_hsa_circ_293568,RMVar_hsa_circ_262636,RMVar_hsa_circ_262637,RMVar_hsa_circ_376050 40565 RMVar_ID_40565 Human_SNP_ID_717260488 A-to-I Human chrX + 54532760 54532760 54532760 TCAGTTCACTGCAACCTCCGCCTCCCGGTTTCAAGCATTTCCTGCCTCAGCCTACCGAGTAGCTG TCAGTTCACTGCAACCTCCGCCTCCCGGTTTCGAGCATTTCCTGCCTCAGCCTACCGAGTAGCTG A G GNL3L Ensembl:ENSG00000130119 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1363833302 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26285178 RMVar_hsa_circ_262642,RMVar_hsa_circ_121676,RMVar_hsa_circ_262643,RMVar_hsa_circ_101443 40566 RMVar_ID_40566 Human_SNP_ID_717263144 A-to-I Human chrX + 54547576 54547576 54547576 AAAATACAAAAGTTAGCCGGGTGTGGTGGTGCATGCCTGTAGTCCCAGCTACTTGGGATGTTGAG AAAATACAAAAGTTAGCCGGGTGTGGTGGTGCCTGCCTGTAGTCCCAGCTACTTGGGATGTTGAG A C GNL3L Ensembl:ENSG00000130119 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs751892821 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89677,RMVar_hsa_circ_262643,RMVar_hsa_circ_101443,RMVar_hsa_circ_80275,RMVar_hsa_circ_262644,RMVar_hsa_circ_262645 40567 RMVar_ID_40567 Human_SNP_ID_717264884 A-to-I Human chrX + 54557121 54557121 54557121 GGAGGATTGCTTGAACCTAGGAGGCACAGGCTACAGTGAGCCAAGATCATACCACTGCACTCCAT GGAGGATTGCTTGAACCTAGGAGGCACAGGCTGCAGTGAGCCAAGATCATACCACTGCACTCCAT A G GNL3L Ensembl:ENSG00000130119 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1280077130 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89677,RMVar_hsa_circ_18955,RMVar_hsa_circ_80275,RMVar_hsa_circ_262644,RMVar_hsa_circ_262645 40568 RMVar_ID_40568 Human_SNP_ID_717265542 A-to-I Human chrX + 54560763 54560763 54560763 CTCCCCCTCCTCCAGTAAAAACAGTCCCGGCTAGGTGCTGTGGCTCACGTCTGTAATCCCAGCAC CTCCCCCTCCTCCAGTAAAAACAGTCCCGGCTGGGTGCTGTGGCTCACGTCTGTAATCCCAGCAC A G GNL3L Ensembl:ENSG00000130119 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs3209039 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_736747,Human_RBP_ID_8011148,Human_RBP_ID_26572246 RMVar_hsa_circ_89677,RMVar_hsa_circ_80275,RMVar_hsa_circ_262644,RMVar_hsa_circ_262645 40569 RMVar_ID_40569 Human_SNP_ID_717265567 A-to-I Human chrX + 54560887 54560878 54560888 ACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAAAATTTAGCCGTGCTTAGTGGCACCTATA ACATGGTGAAACCCCGTCTCTACT__________AAAAATTTAGCCGTGCTTAGTGGCACCTATA TAAAAATACAA T GNL3L Ensembl:ENSG00000130119 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928918075 Functional Loss DEL dbSNP153 25..34 33 - - - Human_RBP_ID_22841815,Human_RBP_ID_23203534,Human_RBP_ID_26572248 RMVar_hsa_circ_89677,RMVar_hsa_circ_80275,RMVar_hsa_circ_262644,RMVar_hsa_circ_262645 40570 RMVar_ID_40570 Human_SNP_ID_717265568 A-to-I Human chrX + 54560879 54560878 54560879 CCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAAAATTTAGCCGTGCTTAGTGG CCTGGCCAACATGGTGAAACCCCGTCTCTACT_AAAATACAAAAAAATTTAGCCGTGCTTAGTGG TA T GNL3L Ensembl:ENSG00000130119 Protein coding intron GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-Seq:(High) rs1385132285 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_22841815 RMVar_hsa_circ_89677,RMVar_hsa_circ_80275,RMVar_hsa_circ_262644,RMVar_hsa_circ_262645 40571 RMVar_ID_40571 Human_SNP_ID_717265578 A-to-I Human chrX + 54560917 54560917 54560917 ACAAAAAAATTTAGCCGTGCTTAGTGGCACCTATAATCCCAGCTACTTGGGAGGCTGAGGCAGGA ACAAAAAAATTTAGCCGTGCTTAGTGGCACCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGA A G GNL3L Ensembl:ENSG00000130119 Protein coding intron GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs934493301 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22734425 RMVar_hsa_circ_89677,RMVar_hsa_circ_80275,RMVar_hsa_circ_262644,RMVar_hsa_circ_262645 40572 RMVar_ID_40572 Human_SNP_ID_717265582 A-to-I Human chrX + 54560973 54560941 54560973 GAGGCAGGAGAATCGCCTGAACCTGGGAGACTAAGGCAGGAGAATCGCCTGAACCTGGGAGGCAG G________________________________AGGCAGGAGAATCGCCTGAACCTGGGAGGCAG GAGGCAGGAGAATCGCCTGAACCTGGGAGACTA G GNL3L Ensembl:ENSG00000130119 Protein coding intron GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-Seq:(High) rs1390328486 Functional Loss DEL dbSNP153 2..33 33 - - - Human_RBP_ID_5068858,Human_RBP_ID_17580298,Human_RBP_ID_22372727,Human_RBP_ID_22734425,Human_RBP_ID_26572249,Human_RBP_ID_27552673 RMVar_hsa_circ_89677,RMVar_hsa_circ_80275,RMVar_hsa_circ_262644,RMVar_hsa_circ_262645 40573 RMVar_ID_40573 Human_SNP_ID_717265598 A-to-I Human chrX + 54561060 54561060 54561060 CACCATTGCACTCTAGCCTGGGCAACAACACGAAACTCCGTCCCAAAAAAAAAAAAAAAAAAAAA CACCATTGCACTCTAGCCTGGGCAACAACACGGAACTCCGTCCCAAAAAAAAAAAAAAAAAAAAA A G GNL3L Ensembl:ENSG00000130119 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs756669305 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23108829,Human_RBP_ID_23203537,Human_RBP_ID_27552674 RMVar_hsa_circ_89677,RMVar_hsa_circ_80275,RMVar_hsa_circ_262644,RMVar_hsa_circ_262645 40574 RMVar_ID_40574 Human_SNP_ID_717265767 A-to-I Human chrX + 54562110 54562110 54562110 CTCTGTTGCCCAGGCTGGAGTGCAATGGCGTGATCTCGGCTCACTGCAACCTCTGCCTCCCGGGT CTCTGTTGCCCAGGCTGGAGTGCAATGGCGTGGTCTCGGCTCACTGCAACCTCTGCCTCCCGGGT A G GNL3L Ensembl:ENSG00000130119 Protein coding intron GSE100210;GSE99789;GSE123020:GSM3490829,GSM3490830,GSM3490831 HepG2 cell line;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109 cell line - 29129909,29796672,32596459 RNA-Seq:(High) rs965866716 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89677,RMVar_hsa_circ_80275,RMVar_hsa_circ_262644,RMVar_hsa_circ_262645 40575 RMVar_ID_40575 Human_SNP_ID_717265790 A-to-I Human chrX + 54562220 54562220 54562220 GGCACCTGCCACCACGCCTGGCTAGTTTTTGTATTTTTAGTAGAGACGATGTTTCACCATGTTGA GGCACCTGCCACCACGCCTGGCTAGTTTTTGTGTTTTTAGTAGAGACGATGTTTCACCATGTTGA A G GNL3L Ensembl:ENSG00000130119 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1350971798 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27149777 RMVar_hsa_circ_89677,RMVar_hsa_circ_80275,RMVar_hsa_circ_262644,RMVar_hsa_circ_262645 40576 RMVar_ID_40576 Human_SNP_ID_717265792 A-to-I Human chrX + 54562226 54562225 54562226 TGCCACCACGCCTGGCTAGTTTTTGTATTTTTAGTAGAGACGATGTTTCACCATGTTGACCAGGC TGCCACCACGCCTGGCTAGTTTTTGTATTTTT_GTAGAGACGATGTTTCACCATGTTGACCAGGC TA T GNL3L Ensembl:ENSG00000130119 Protein coding intron GSE47997;GSE38233;GSE100210;GSE99789;GSE123020:GSM3490829,GSM3490830,GSM3490831 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109 cell line - 23474544,24183664,29129909,29796672,32596459 RNA-Seq:(High) rs1236258416 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_27149777 RMVar_hsa_circ_89677,RMVar_hsa_circ_80275,RMVar_hsa_circ_262644,RMVar_hsa_circ_262645 40577 RMVar_ID_40577 Human_SNP_ID_717265793 A-to-I Human chrX + 54562226 54562226 54562226 TGCCACCACGCCTGGCTAGTTTTTGTATTTTTAGTAGAGACGATGTTTCACCATGTTGACCAGGC TGCCACCACGCCTGGCTAGTTTTTGTATTTTTGGTAGAGACGATGTTTCACCATGTTGACCAGGC A G GNL3L Ensembl:ENSG00000130119 Protein coding intron GSE47997;GSE38233;GSE100210;GSE99789;GSE123020:GSM3490829,GSM3490830,GSM3490831 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109 cell line - 23474544,24183664,29129909,29796672,32596459 RNA-Seq:(High) rs948208465 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27149777 RMVar_hsa_circ_89677,RMVar_hsa_circ_80275,RMVar_hsa_circ_262644,RMVar_hsa_circ_262645 40578 RMVar_ID_40578 Human_SNP_ID_717265797 A-to-I Human chrX + 54562243 54562243 54562243 AGTTTTTGTATTTTTAGTAGAGACGATGTTTCACCATGTTGACCAGGCTGGTCTCGAACTCTTGA AGTTTTTGTATTTTTAGTAGAGACGATGTTTCGCCATGTTGACCAGGCTGGTCTCGAACTCTTGA A G GNL3L Ensembl:ENSG00000130119 Protein coding intron GSE47997;GSE38233;GSE100210;GSE99789 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 23474544,24183664,29129909,29796672 RNA-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 40579 RMVar_ID_40579 Human_SNP_ID_717265805 A-to-I Human chrX + 54562285 54562285 54562285 CCAGGCTGGTCTCGAACTCTTGACCTCAAGTGATCCACTCGCTTCGGCCTCCCAAAGTGCTGGGA CCAGGCTGGTCTCGAACTCTTGACCTCAAGTGTTCCACTCGCTTCGGCCTCCCAAAGTGCTGGGA A T GNL3L Ensembl:ENSG00000130119 Protein coding intron GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs950928922 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2506978,Human_miRNA_ID_3043547 RMVar_hsa_circ_89677,RMVar_hsa_circ_80275,RMVar_hsa_circ_262644,RMVar_hsa_circ_262645 40580 RMVar_ID_40580 Human_SNP_ID_717265809 A-to-I Human chrX + 54562320 54562320 54562320 CACTCGCTTCGGCCTCCCAAAGTGCTGGGATTATAGGCGTGAGCCACTGTGCCCAGCCTCACAGC CACTCGCTTCGGCCTCCCAAAGTGCTGGGATTTTAGGCGTGAGCCACTGTGCCCAGCCTCACAGC A T GNL3L Ensembl:ENSG00000130119 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1569542215 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23203560,Human_RBP_ID_27383204 Human_miRNA_ID_1997195,Human_miRNA_ID_2229688,Human_miRNA_ID_2505661 RMVar_hsa_circ_89677,RMVar_hsa_circ_80275,RMVar_hsa_circ_262644,RMVar_hsa_circ_262645 40581 RMVar_ID_40581 Human_SNP_ID_717265882 A-to-I Human chrX + 54562734 54562734 54562734 AGAATCACTTGATCTCAGGAGGCGGAGGTTGCAGTGAGTCGACATCACACCACTGCACTCCAGCC AGAATCACTTGATCTCAGGAGGCGGAGGTTGCGGTGAGTCGACATCACACCACTGCACTCCAGCC A G GNL3L Ensembl:ENSG00000130119 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs769095946 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89677,RMVar_hsa_circ_80275,RMVar_hsa_circ_262644,RMVar_hsa_circ_262645 40582 RMVar_ID_40582 Human_SNP_ID_717265966 A-to-I Human chrX + 54563126 54563126 54563126 TATTTCACACTATCTCATTGAACTCTCCTGGTATGTGATAGTGTTATAATGAAAAATTGCATACC TATTTCACACTATCTCATTGAACTCTCCTGGTGTGTGATAGTGTTATAATGAAAAATTGCATACC A G GNL3L Ensembl:ENSG00000130119 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1389311896 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_736760,Human_RBP_ID_1342624,Human_RBP_ID_1716612,Human_RBP_ID_8011202,Human_RBP_ID_16911184,Human_RBP_ID_17555013,Human_RBP_ID_17718544,Human_RBP_ID_18152575,Human_RBP_ID_18406066,Human_RBP_ID_23203583,Human_RBP_ID_26572293,Human_RBP_ID_27794244 RMVar_hsa_circ_89677,RMVar_hsa_circ_80275,RMVar_hsa_circ_262644,RMVar_hsa_circ_262645 40583 RMVar_ID_40583 Human_SNP_ID_717265992 A-to-I Human chrX + 54563297 54563297 54563297 AAGCAGTATACATTCAGAATGCACCTCTACTTATGATGGGGCTACTTCCTGGTAAACCCATTGTA AAGCAGTATACATTCAGAATGCACCTCTACTTGTGATGGGGCTACTTCCTGGTAAACCCATTGTA A G GNL3L Ensembl:ENSG00000130119 Protein coding intron GSE38233;GSE100210;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,temporal_cortex - 24183664,29129909,30559470 RNA-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 40584 RMVar_ID_40584 Human_SNP_ID_717266030 A-to-I Human chrX + 54563515 54563515 54563515 GTAAGAATTTGGGACTGCAGGCCAGTTACGATAGCTCTCACCTGTAATCCCAGCATTTTGGGAGG GTAAGAATTTGGGACTGCAGGCCAGTTACGATGGCTCTCACCTGTAATCCCAGCATTTTGGGAGG A G GNL3L Ensembl:ENSG00000130119 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1137144 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8011217,Human_RBP_ID_16911209,Human_RBP_ID_18152583,Human_RBP_ID_23203592,Human_RBP_ID_26572301 Human_miRNA_ID_2891460 RMVar_hsa_circ_89677,RMVar_hsa_circ_80275,RMVar_hsa_circ_262644,RMVar_hsa_circ_262645 40585 RMVar_ID_40585 Human_SNP_ID_717266034 A-to-I Human chrX + 54563555 54563555 54563555 CCTGTAATCCCAGCATTTTGGGAGGCCGAGGCAGGCGGATCACTTGAGGTCAGGAGTTCAAGACC CCTGTAATCCCAGCATTTTGGGAGGCCGAGGCGGGCGGATCACTTGAGGTCAGGAGTTCAAGACC A G GNL3L Ensembl:ENSG00000130119 Protein coding intron GSE38233;GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,32596459 RNA-Seq:(High) rs1137146 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89677,RMVar_hsa_circ_80275,RMVar_hsa_circ_262644,RMVar_hsa_circ_262645 40586 RMVar_ID_40586 Human_SNP_ID_717266054 A-to-I Human chrX + 54563630 54563630 54563630 ATATGGCGAAACCTCATCTCTACCAAAAAAATACAAAGATTAGCTGGGCATGGTGTCTCATGCCT ATATGGCGAAACCTCATCTCTACCAAAAAAATGCAAAGATTAGCTGGGCATGGTGTCTCATGCCT A G GNL3L Ensembl:ENSG00000130119 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1569542237 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5068952,Human_RBP_ID_18152584 RMVar_hsa_circ_89677,RMVar_hsa_circ_80275,RMVar_hsa_circ_262644,RMVar_hsa_circ_262645 40587 RMVar_ID_40587 Human_SNP_ID_717266055 A-to-I Human chrX + 54563632 54563632 54563632 ATGGCGAAACCTCATCTCTACCAAAAAAATACAAAGATTAGCTGGGCATGGTGTCTCATGCCTGT ATGGCGAAACCTCATCTCTACCAAAAAAATACGAAGATTAGCTGGGCATGGTGTCTCATGCCTGT A G GNL3L Ensembl:ENSG00000130119 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1387986529 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18152584 RMVar_hsa_circ_89677,RMVar_hsa_circ_80275,RMVar_hsa_circ_262644,RMVar_hsa_circ_262645 40588 RMVar_ID_40588 Human_SNP_ID_717266058 A-to-I Human chrX + 54563647 54563643 54563648 CTCTACCAAAAAAATACAAAGATTAGCTGGGCATGGTGTCTCATGCCTGTAGTCCCAGCTACCTA CTCTACCAAAAAAATACAAAGATTAGCTG_____GGTGTCTCATGCCTGTAGTCCCAGCTACCTA GGGCAT G GNL3L Ensembl:ENSG00000130119 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-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 40589 RMVar_ID_40589 Human_SNP_ID_717266059 A-to-I Human chrX + 54563647 54563647 54563647 CTCTACCAAAAAAATACAAAGATTAGCTGGGCATGGTGTCTCATGCCTGTAGTCCCAGCTACCTA CTCTACCAAAAAAATACAAAGATTAGCTGGGCGTGGTGTCTCATGCCTGTAGTCCCAGCTACCTA A G GNL3L Ensembl:ENSG00000130119 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-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 40590 RMVar_ID_40590 Human_SNP_ID_717266062 A-to-I Human chrX + 54563657 54563657 54563657 AAAATACAAAGATTAGCTGGGCATGGTGTCTCATGCCTGTAGTCCCAGCTACCTATGGGGCTGAG AAAATACAAAGATTAGCTGGGCATGGTGTCTCGTGCCTGTAGTCCCAGCTACCTATGGGGCTGAG A G GNL3L Ensembl:ENSG00000130119 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941958566 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89677,RMVar_hsa_circ_80275,RMVar_hsa_circ_262644,RMVar_hsa_circ_262645 40591 RMVar_ID_40591 Human_SNP_ID_717266226 A-to-I Human chrX + 54564424 54564422 54564424 TCTTCGTTCTCTTTTTTTTTTTTTTTTTTTTGAGACAGAGTCTAGCTCTGTTGTCCAGGCTGGAG TCTTCGTTCTCTTTTTTTTTTTTTTTTTTTT__GACAGAGTCTAGCTCTGTTGTCCAGGCTGGAG TGA T GNL3L Ensembl:ENSG00000130119 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1420753053 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_16964747 RMVar_hsa_circ_89677,RMVar_hsa_circ_80275,RMVar_hsa_circ_262644,RMVar_hsa_circ_262645 40592 RMVar_ID_40592 Human_SNP_ID_717266228 A-to-I Human chrX + 54564424 54564424 54564424 TCTTCGTTCTCTTTTTTTTTTTTTTTTTTTTGAGACAGAGTCTAGCTCTGTTGTCCAGGCTGGAG TCTTCGTTCTCTTTTTTTTTTTTTTTTTTTTGTGACAGAGTCTAGCTCTGTTGTCCAGGCTGGAG A T GNL3L Ensembl:ENSG00000130119 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170937284 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16964747 RMVar_hsa_circ_89677,RMVar_hsa_circ_80275,RMVar_hsa_circ_262644,RMVar_hsa_circ_262645 40593 RMVar_ID_40593 Human_SNP_ID_717266231 A-to-I Human chrX + 54564428 54564427 54564429 CGTTCTCTTTTTTTTTTTTTTTTTTTTGAGACAGAGTCTAGCTCTGTTGTCCAGGCTGGAGTGGT CGTTCTCTTTTTTTTTTTTTTTTTTTTGAGAC__AGTCTAGCTCTGTTGTCCAGGCTGGAGTGGT CAG C GNL3L Ensembl:ENSG00000130119 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1246239189 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_8011253,Human_RBP_ID_16964748,Human_RBP_ID_26572331 Human_miRNA_ID_2510078 RMVar_hsa_circ_89677,RMVar_hsa_circ_80275,RMVar_hsa_circ_262644,RMVar_hsa_circ_262645 40594 RMVar_ID_40594 Human_SNP_ID_717266232 A-to-I Human chrX + 54564428 54564428 54564428 CGTTCTCTTTTTTTTTTTTTTTTTTTTGAGACAGAGTCTAGCTCTGTTGTCCAGGCTGGAGTGGT CGTTCTCTTTTTTTTTTTTTTTTTTTTGAGACGGAGTCTAGCTCTGTTGTCCAGGCTGGAGTGGT A G GNL3L Ensembl:ENSG00000130119 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1323064295 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8011253,Human_RBP_ID_16964748,Human_RBP_ID_26572331 Human_miRNA_ID_2510078 RMVar_hsa_circ_89677,RMVar_hsa_circ_80275,RMVar_hsa_circ_262644,RMVar_hsa_circ_262645 40595 RMVar_ID_40595 Human_SNP_ID_717266249 A-to-I Human chrX + 54564500 54564500 54564500 CGTGATCTCGGTTCACTGCAACCTCCGCCTCCAGGGTTCAAGCGGTTCTCCTGCCTCAGCCTCCC CGTGATCTCGGTTCACTGCAACCTCCGCCTCCTGGGTTCAAGCGGTTCTCCTGCCTCAGCCTCCC A T GNL3L Ensembl:ENSG00000130119 Protein coding intron GSE100210;GSE99789;GSE123020:GSM3490829,GSM3490830,GSM3490831 HepG2 cell line;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109 cell line - 29129909,29796672,32596459 RNA-Seq:(High) rs1202644723 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89677,RMVar_hsa_circ_80275,RMVar_hsa_circ_262644,RMVar_hsa_circ_262645 40596 RMVar_ID_40596 Human_SNP_ID_717266285 A-to-I Human chrX + 54564680 54564680 54564680 CTCCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAAGAGTGAGCCACTGCGCCTGGCCTTTTTCT CTCCTGCCTCAGCCTCCCAAAGTGCTGGGATTGCAAGAGTGAGCCACTGCGCCTGGCCTTTTTCT A G GNL3L Ensembl:ENSG00000130119 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1569542258 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8011255,Human_RBP_ID_10467325,Human_RBP_ID_16911265,Human_RBP_ID_23203619,Human_RBP_ID_26285340,Human_RBP_ID_26572332 RMVar_hsa_circ_89677,RMVar_hsa_circ_80275,RMVar_hsa_circ_262644,RMVar_hsa_circ_262645 40597 RMVar_ID_40597 Human_SNP_ID_717266329 A-to-I Human chrX + 54564820 54564820 54564820 CAGTGGCGTGATCTTGGCTCACTGCAACCTCCACCTCCTGGGTTCAAGCGATTCTCCTGCCTTAG CAGTGGCGTGATCTTGGCTCACTGCAACCTCCCCCTCCTGGGTTCAAGCGATTCTCCTGCCTTAG A C GNL3L Ensembl:ENSG00000130119 Protein coding intron GSE123020:GSM3490829,GSM3490830,GSM3490831 esophageal squamous carcinoma cells,EC109 cell line - 32596459 RNA-Seq:(High) rs1448412345 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89677,RMVar_hsa_circ_80275,RMVar_hsa_circ_262644,RMVar_hsa_circ_262645 40598 RMVar_ID_40598 Human_SNP_ID_717266330 A-to-I Human chrX + 54564820 54564820 54564820 CAGTGGCGTGATCTTGGCTCACTGCAACCTCCACCTCCTGGGTTCAAGCGATTCTCCTGCCTTAG CAGTGGCGTGATCTTGGCTCACTGCAACCTCCGCCTCCTGGGTTCAAGCGATTCTCCTGCCTTAG A G GNL3L Ensembl:ENSG00000130119 Protein coding intron GSE123020:GSM3490829,GSM3490830,GSM3490831 esophageal squamous carcinoma cells,EC109 cell line - 32596459 RNA-Seq:(High) rs1448412345 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89677,RMVar_hsa_circ_80275,RMVar_hsa_circ_262644,RMVar_hsa_circ_262645 40599 RMVar_ID_40599 Human_SNP_ID_717266344 A-to-I Human chrX + 54564919 54564919 54564919 CCATGCTGGGCTAATTTTTGTATTTTTAGTAGAGGCGGGGGTTTCTCCACACTGGCCAGGCTGGT CCATGCTGGGCTAATTTTTGTATTTTTAGTAGTGGCGGGGGTTTCTCCACACTGGCCAGGCTGGT A T GNL3L Ensembl:ENSG00000130119 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1293065895 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_736768,Human_RBP_ID_16911276,Human_RBP_ID_23203624,Human_RBP_ID_24527087 RMVar_hsa_circ_89677,RMVar_hsa_circ_80275,RMVar_hsa_circ_262644,RMVar_hsa_circ_262645 40600 RMVar_ID_40600 Human_SNP_ID_717266352 A-to-I Human chrX + 54564937 54564937 54564937 TGTATTTTTAGTAGAGGCGGGGGTTTCTCCACACTGGCCAGGCTGGTCTTGAACTTCTGACCTCA TGTATTTTTAGTAGAGGCGGGGGTTTCTCCACGCTGGCCAGGCTGGTCTTGAACTTCTGACCTCA A G GNL3L Ensembl:ENSG00000130119 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs926485645 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_736768,Human_RBP_ID_5068973,Human_RBP_ID_8011263,Human_RBP_ID_16911280,Human_RBP_ID_24527087,Human_RBP_ID_26572338 Human_miRNA_ID_2176176,Human_miRNA_ID_2179620 RMVar_hsa_circ_89677,RMVar_hsa_circ_80275,RMVar_hsa_circ_262644,RMVar_hsa_circ_262645 40601 RMVar_ID_40601 Human_SNP_ID_717266447 A-to-I Human chrX + 54565582 54565582 54565582 GTCTTGAACTGCTGGCCTCAAGTAATCCTCCCATCTCGGTCTCCCAAAGTGCTAGGATTACAGGT GTCTTGAACTGCTGGCCTCAAGTAATCCTCCCGTCTCGGTCTCCCAAAGTGCTAGGATTACAGGT A G GNL3L Ensembl:ENSG00000130119 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417429919 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_736779,Human_RBP_ID_8011287,Human_RBP_ID_16911334 RMVar_hsa_circ_89677,RMVar_hsa_circ_80275,RMVar_hsa_circ_262644,RMVar_hsa_circ_262645 40602 RMVar_ID_40602 Human_SNP_ID_717266450 A-to-I Human chrX + 54565603 54565603 54565603 GTAATCCTCCCATCTCGGTCTCCCAAAGTGCTAGGATTACAGGTGTGAGCCACCATGCCCAGCCA GTAATCCTCCCATCTCGGTCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCATGCCCAGCCA A G GNL3L Ensembl:ENSG00000130119 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982044086 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8011287 RMVar_hsa_circ_89677,RMVar_hsa_circ_80275,RMVar_hsa_circ_262644,RMVar_hsa_circ_262645 40603 RMVar_ID_40603 Human_SNP_ID_717266534 A-to-I Human chrX + 54565993 54565993 54565993 CAGGCGCAGGCCACCATGCTTGGCTAACTTTTATATTTTTACCAGAGACAAGGTTTCACCATGTT CAGGCGCAGGCCACCATGCTTGGCTAACTTTTGTATTTTTACCAGAGACAAGGTTTCACCATGTT A G GNL3L Ensembl:ENSG00000130119 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005689546 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1062998,Human_RBP_ID_1405901,Human_RBP_ID_8011300,Human_RBP_ID_16911356,Human_RBP_ID_17555035,Human_RBP_ID_18152595,Human_RBP_ID_27794268 RMVar_hsa_circ_89677,RMVar_hsa_circ_80275,RMVar_hsa_circ_262644,RMVar_hsa_circ_262645 40604 RMVar_ID_40604 Human_SNP_ID_717266538 A-to-I Human chrX + 54566010 54566009 54566010 GCTTGGCTAACTTTTATATTTTTACCAGAGACAAGGTTTCACCATGTTGGCAAGGCTGGTCTTGA GCTTGGCTAACTTTTATATTTTTACCAGAGAC_AGGTTTCACCATGTTGGCAAGGCTGGTCTTGA CA C GNL3L Ensembl:ENSG00000130119 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1485445721 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_16911358,Human_RBP_ID_17555035,Human_RBP_ID_22841821,Human_RBP_ID_26572350,Human_RBP_ID_27794268 RMVar_hsa_circ_89677,RMVar_hsa_circ_80275,RMVar_hsa_circ_262644,RMVar_hsa_circ_262645 40605 RMVar_ID_40605 Human_SNP_ID_717266551 A-to-I Human chrX + 54566082 54566082 54566082 ACCTCAAGTGATACACCCGTCTTAGCCTCCCAAAGTTCTGGGATTACAGGCATGAGCCATTGTGC ACCTCAAGTGATACACCCGTCTTAGCCTCCCAGAGTTCTGGGATTACAGGCATGAGCCATTGTGC A G GNL3L Ensembl:ENSG00000130119 Protein coding intron GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs1384732279 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16911366 RMVar_hsa_circ_89677,RMVar_hsa_circ_80275,RMVar_hsa_circ_262644,RMVar_hsa_circ_262645 40606 RMVar_ID_40606 Human_SNP_ID_717267026 A-to-I Human chrX + 54568836 54568836 54568836 GGGCCTCCCAAGGTGCTGGGATTATAGGCGTGAGCCACGACGCCTGGCCAACAATGTAGTATTTT GGGCCTCCCAAGGTGCTGGGATTATAGGCGTGGGCCACGACGCCTGGCCAACAATGTAGTATTTT A G GNL3L Ensembl:ENSG00000130119 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1271972825 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16964772 40607 RMVar_ID_40607 Human_SNP_ID_717271113 A-to-I Human chrX + 54590970 54590970 54590970 CTCCTGCCTCAGCCTCCTGAGTAACTGGGACTACAGATGCACACCACCACAGCTGGCAGATTTTT CTCCTGCCTCAGCCTCCTGAGTAACTGGGACTGCAGATGCACACCACCACAGCTGGCAGATTTTT A G GNL3L Ensembl:ENSG00000130119 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1207184740 Functional Loss SNV dbSNP153 33..33 33 - - - 40608 RMVar_ID_40608 Human_SNP_ID_717487777 A-to-I Human chrX - 55749905 55749905 55749905 GGTCTCTGGTTTTCCTAGGCAGAGGACCCTGCAGCCTTCCGCAGTGTTTGTGTCCCTGGGTACTT GGTCTCTGGTTTTCCTAGGCAGAGGACCCTGCTGCCTTCCGCAGTGTTTGTGTCCCTGGGTACTT T A - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1441730615 Functional Loss SNV dbSNP153 33..33 33 - - - 40609 RMVar_ID_40609 Human_SNP_ID_717487778 A-to-I Human chrX - 55749905 55749905 55749905 GGTCTCTGGTTTTCCTAGGCAGAGGACCCTGCAGCCTTCCGCAGTGTTTGTGTCCCTGGGTACTT GGTCTCTGGTTTTCCTAGGCAGAGGACCCTGCGGCCTTCCGCAGTGTTTGTGTCCCTGGGTACTT T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1441730615 Functional Loss SNV dbSNP153 33..33 33 - - - 40610 RMVar_ID_40610 Human_SNP_ID_717815361 A-to-I Human chrX - 57077512 57077512 57077512 CATGTTTATAGCAGCACAATTCACAACTGCAAAAATACGGAACCAATGTAAGTGCCCATCAACCA CATGTTTATAGCAGCACAATTCACAACTGCAAGAATACGGAACCAATGTAAGTGCCCATCAACCA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1169845295 Functional Loss SNV dbSNP153 33..33 33 - - - 40611 RMVar_ID_40611 Human_SNP_ID_717815392 A-to-I Human chrX - 57077645 57077645 57077645 AACTACCATGGAACACAGTATGGAGAGTCATTAAAGAACTAATGTAGAACTACAACTTGATCCAG AACTACCATGGAACACAGTATGGAGAGTCATTGAAGAACTAATGTAGAACTACAACTTGATCCAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1434670870 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3260351,Human_RBP_ID_18922181 40612 RMVar_ID_40612 Human_SNP_ID_717815542 A-to-I Human chrX - 57078266 57078266 57078266 AAACCAGTTCCTCATCTCTCACCTCATACAAAAATCAACTCAAGATGGATCAAAGACTTAAATCT AAACCAGTTCCTCATCTCTCACCTCATACAAACATCAACTCAAGATGGATCAAAGACTTAAATCT T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs901109654 Functional Loss SNV dbSNP153 33..33 33 - - - 40613 RMVar_ID_40613 Human_SNP_ID_717817233 A-to-I Human chrX - 57085284 57085284 57085284 TTTGTCTAATATTATCATCAGTAGGGTGTTAAAGTCTGTCACTATTATTGTGTGGGAGTCTAAGT TTTGTCTAATATTATCATCAGTAGGGTGTTAACGTCTGTCACTATTATTGTGTGGGAGTCTAAGT T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1216627798 Functional Loss SNV dbSNP153 33..33 33 - - - 40614 RMVar_ID_40614 Human_SNP_ID_717828359 A-to-I Human chrX + 57139571 57139571 57139571 CTTCTCCTGGGTTCACGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGAACCACAGGTGCCCG CTTCTCCTGGGTTCACGCCATTCTCCTGCCTCGGCCTCCCGAGTAGCTGGAACCACAGGTGCCCG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1331391389 Functional Loss SNV dbSNP153 33..33 33 - - - 40615 RMVar_ID_40615 Human_SNP_ID_717828367 A-to-I Human chrX + 57139589 57139589 57139589 CATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGAACCACAGGTGCCCGCCACCACACTGGGCTAAT CATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACCACAGGTGCCCGCCACCACACTGGGCTAAT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs948368530 Functional Loss SNV dbSNP153 33..33 33 - - - 40616 RMVar_ID_40616 Human_SNP_ID_717828368 A-to-I Human chrX + 57139589 57139589 57139589 CATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGAACCACAGGTGCCCGCCACCACACTGGGCTAAT CATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGTACCACAGGTGCCCGCCACCACACTGGGCTAAT A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs948368530 Functional Loss SNV dbSNP153 33..33 33 - - - 40617 RMVar_ID_40617 Human_SNP_ID_717838316 A-to-I Human chrX + 57180501 57180501 57180501 AATCATATTATTATGAACACCTCTATGCACACAACTAAAAAATCAAGAAGAAATGGAAGAATTCC AATCATATTATTATGAACACCTCTATGCACACCACTAAAAAATCAAGAAGAAATGGAAGAATTCC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs896890441 Functional Loss SNV dbSNP153 33..33 33 - - - 40618 RMVar_ID_40618 Human_SNP_ID_717846425 A-to-I Human chrX + 57215177 57215177 57215177 GTGGGGAAAGAACATAAACAGGCACTTCCCAAAAGAAGACATTTATGTGACCAACAAACATATGA GTGGGGAAAGAACATAAACAGGCACTTCCCAAGAGAAGACATTTATGTGACCAACAAACATATGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs182772394 Functional Loss SNV dbSNP153 33..33 33 - - - 40619 RMVar_ID_40619 Human_SNP_ID_717846464 A-to-I Human chrX + 57215416 57215415 57215416 AACCATTGTGGAAGACAGTGTGGCAATTCCTCAAAAACCTACAATCAGAAATACCATTTGACCCG AACCATTGTGGAAGACAGTGTGGCAATTCCTC_AAAACCTACAATCAGAAATACCATTTGACCCG CA C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1198025734 Functional Loss DEL dbSNP153 33..33 33 - - - 40620 RMVar_ID_40620 Human_SNP_ID_717847194 A-to-I Human chrX + 57217177 57217177 57217177 TTTGTTTGAGTTCGTTGTAGAGTCTGGATATTAGTCCTTTGTCAGATGTATAGATTGTGAAGATT TTTGTTTGAGTTCGTTGTAGAGTCTGGATATTCGTCCTTTGTCAGATGTATAGATTGTGAAGATT A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs966747658 Functional Loss SNV dbSNP153 33..33 33 - - - 40621 RMVar_ID_40621 Human_SNP_ID_717851350 A-to-I Human chrX + 57234917 57234917 57234917 AAAATTAACCGAGCATGGTGGTGCACCCTAGTAATCCTAGCTACTAGGGAGGCTGAGACAGGAAA AAAATTAACCGAGCATGGTGGTGCACCCTAGTTATCCTAGCTACTAGGGAGGCTGAGACAGGAAA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1365295982 Functional Loss SNV dbSNP153 33..33 33 - - - 40622 RMVar_ID_40622 Human_SNP_ID_717851355 A-to-I Human chrX + 57234927 57234927 57234927 GAGCATGGTGGTGCACCCTAGTAATCCTAGCTACTAGGGAGGCTGAGACAGGAAAATTGCTTGAA GAGCATGGTGGTGCACCCTAGTAATCCTAGCTTCTAGGGAGGCTGAGACAGGAAAATTGCTTGAA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs999127260 Functional Loss SNV dbSNP153 33..33 33 - - - 40623 RMVar_ID_40623 Human_SNP_ID_717891318 A-to-I Human chrX + 57393611 57393611 57393611 GATTGGGCTTGATTGTGTCCTTCATAAGCACTATCAATGCACCACTCACCCCCAGATCTTCAGCA GATTGGGCTTGATTGTGTCCTTCATAAGCACTGTCAATGCACCACTCACCCCCAGATCTTCAGCA A G FAAH2 Ensembl:ENSG00000165591 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1419238515 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6235,RMVar_hsa_circ_262686,RMVar_hsa_circ_262687 40624 RMVar_ID_40624 Human_SNP_ID_717891326 A-to-I Human chrX + 57393640 57393640 57393640 ACTATCAATGCACCACTCACCCCCAGATCTTCAGCACTGACGGGGTCTCCTTTCTTACTGGATGC ACTATCAATGCACCACTCACCCCCAGATCTTCGGCACTGACGGGGTCTCCTTTCTTACTGGATGC A G FAAH2 Ensembl:ENSG00000165591 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1263497523 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6235,RMVar_hsa_circ_262686,RMVar_hsa_circ_262687 40625 RMVar_ID_40625 Human_SNP_ID_717891361 A-to-I Human chrX - 57393776 57393776 57393776 TGGACAGGCTCCAACGAAGAAAAGTCACACACAGACGGTCCACTTTGATATCTCTGTGGCCAGTG TGGACAGGCTCCAACGAAGAAAAGTCACACACGGACGGTCCACTTTGATATCTCTGTGGCCAGTG T C MTHFD1P1 Ensembl:ENSG00000231831 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1316336352 Functional Loss SNV dbSNP153 33..33 33 - - - 40626 RMVar_ID_40626 Human_SNP_ID_717891382 A-to-I Human chrX - 57393843 57393843 57393843 ATCCAGAAACCATAGCTTGGCAAAGAGTGTTGAATACCAATGATAGATTCCTGAGGAAGATCACG ATCCAGAAACCATAGCTTGGCAAAGAGTGTTGGATACCAATGATAGATTCCTGAGGAAGATCACG T C MTHFD1P1 Ensembl:ENSG00000231831 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1197828090 Functional Loss SNV dbSNP153 33..33 33 - - - 40627 RMVar_ID_40627 Human_SNP_ID_717950673 A-to-I Human chrX + 57619460 57619460 57619460 ATTTACAACAGCAAAGACATAGGACCAGCCCAAATTTCCATCTATGATAGACTGAATAAGGAAAA ATTTACAACAGCAAAGACATAGGACCAGCCCAGATTTCCATCTATGATAGACTGAATAAGGAAAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1476453481 Functional Loss SNV dbSNP153 33..33 33 - - - 40628 RMVar_ID_40628 Human_SNP_ID_508403993 A-to-I Human chr12 + 80800368 80800368 80800368 AAAATTAGCTGGGTGTGGTGGCGCATGCCTCTAATCCCAACTACTCGGAAGGCTGAGGCAGGAGA AAAATTAGCTGGGTGTGGTGGCGCATGCCTCTGATCCCAACTACTCGGAAGGCTGAGGCAGGAGA A G LINC01490,LINC01490:2 RNACentral:URS0000D5B8F3,RNACentral:URS0000D59467 lincRNA,lincRNA exon,exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs967017636 Functional Loss SNV dbSNP153 33..33 33 - - - 40629 RMVar_ID_40629 Human_SNP_ID_508403994 A-to-I Human chr12 + 80800374 80800374 80800374 AGCTGGGTGTGGTGGCGCATGCCTCTAATCCCAACTACTCGGAAGGCTGAGGCAGGAGAATTGCT AGCTGGGTGTGGTGGCGCATGCCTCTAATCCCTACTACTCGGAAGGCTGAGGCAGGAGAATTGCT A T LINC01490,LINC01490:2 RNACentral:URS0000D5B8F3,RNACentral:URS0000D59467 lincRNA,lincRNA exon,exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1218727180 Functional Loss SNV dbSNP153 33..33 33 - - - 40630 RMVar_ID_40630 Human_SNP_ID_508420452 A-to-I Human chr12 - 80868505 80868505 80868505 GGAGTGCAATGGCGCAATCTCGGCCCACTGCAACCTCCACCTCCCAGGTTCAAACAAGTCTCCCG GGAGTGCAATGGCGCAATCTCGGCCCACTGCACCCTCCACCTCCCAGGTTCAAACAAGTCTCCCG T G LIN7A Ensembl:ENSG00000111052 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1342376061 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54785,RMVar_hsa_circ_60811 40631 RMVar_ID_40631 Human_SNP_ID_508578464 A-to-I Human chr12 - 81508806 81508806 81508806 GAATTGAACAATGAGAACACATGGACACAGGAAGGGGAACATCACACTCTGGGGACTGTTGTGGG GAATTGAACAATGAGAACACATGGACACAGGACGGGGAACATCACACTCTGGGGACTGTTGTGGG T G PPFIA2 Ensembl:ENSG00000139220 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1424823620 Functional Loss SNV dbSNP153 33..33 33 - - - 40632 RMVar_ID_40632 Human_SNP_ID_508578466 A-to-I Human chr12 - 81508810 81508810 81508810 GTGGGAATTGAACAATGAGAACACATGGACACAGGAAGGGGAACATCACACTCTGGGGACTGTTG GTGGGAATTGAACAATGAGAACACATGGACACGGGAAGGGGAACATCACACTCTGGGGACTGTTG T C PPFIA2 Ensembl:ENSG00000139220 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1460973928 Functional Loss SNV dbSNP153 33..33 33 - - - 40633 RMVar_ID_40633 Human_SNP_ID_508578467 A-to-I Human chr12 - 81508810 81508810 81508810 GTGGGAATTGAACAATGAGAACACATGGACACAGGAAGGGGAACATCACACTCTGGGGACTGTTG GTGGGAATTGAACAATGAGAACACATGGACACCGGAAGGGGAACATCACACTCTGGGGACTGTTG T G PPFIA2 Ensembl:ENSG00000139220 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1460973928 Functional Loss SNV dbSNP153 33..33 33 - - - 40634 RMVar_ID_40634 Human_SNP_ID_508599180 A-to-I Human chr12 - 81594729 81594729 81594729 TTTTAATGTTCTGTATAGATGGAAGTCTCACTATATTTTCCAGGGTCTTGAACTCCTGGGCTCAA TTTTAATGTTCTGTATAGATGGAAGTCTCACTGTATTTTCCAGGGTCTTGAACTCCTGGGCTCAA T C PPFIA2 Ensembl:ENSG00000139220 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1222321675 Functional Loss SNV dbSNP153 33..33 33 - - - 40635 RMVar_ID_40635 Human_SNP_ID_508786629 A-to-I Human chr12 - 82353111 82353111 82353111 GTTCCTACAGGTTAAAATATCTGCTGCCTATTAGGTTCTTCTGTGACATGTGCCTCCCAGCAGTG GTTCCTACAGGTTAAAATATCTGCTGCCTATTGGGTTCTTCTGTGACATGTGCCTCCCAGCAGTG T C CCDC59 Ensembl:ENSG00000133773 Protein coding intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1173254123 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_429041,Human_RBP_ID_1802284,Human_RBP_ID_5111800,Human_RBP_ID_6227077,Human_RBP_ID_9365283,Human_RBP_ID_18410726,Human_RBP_ID_18634062,Human_RBP_ID_26321798,Human_RBP_ID_26806979,Human_RBP_ID_26912071 40636 RMVar_ID_40636 Human_SNP_ID_508884064 A-to-I Human chr12 + 82743330 82743330 82743330 GGGAATGGTGGTGCGTTCCTGTAATCATAGCTACTCGGTAGGCTGAGGCAGGAGAATTGCTTAAA GGGAATGGTGGTGCGTTCCTGTAATCATAGCTGCTCGGTAGGCTGAGGCAGGAGAATTGCTTAAA A G TMTC2 Ensembl:ENSG00000179104 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1433751741 Functional Loss SNV dbSNP153 33..33 33 - - - 40637 RMVar_ID_40637 Human_SNP_ID_508919465 A-to-I Human chr12 + 82888488 82888488 82888488 GACTTTGTTTTTTTAAGAGATGAGGTCTCGCTATGTTGTCAAGGCTGATCTTGAACTCTTGGGCT GACTTTGTTTTTTTAAGAGATGAGGTCTCGCTGTGTTGTCAAGGCTGATCTTGAACTCTTGGGCT A G TMTC2 Ensembl:ENSG00000179104 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1171449388 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_309574,RMVar_hsa_circ_348792,RMVar_hsa_circ_299671,RMVar_hsa_circ_158597,RMVar_hsa_circ_49739,RMVar_hsa_circ_158596,RMVar_hsa_circ_158598 40638 RMVar_ID_40638 Human_SNP_ID_509437775 A-to-I Human chr12 - 84861419 84861419 84861419 CATTTGTGCAGAAAGGATTGCAGACAAATCTTAGGAGGGCTGAGGTACATGTTTGCCAGGATTTT CATTTGTGCAGAAAGGATTGCAGACAAATCTTGGGAGGGCTGAGGTACATGTTTGCCAGGATTTT T C SLC6A15 Ensembl:ENSG00000072041 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1431735962 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_429145,Human_RBP_ID_6228047,Human_RBP_ID_8785801,Human_RBP_ID_12046712,Human_RBP_ID_17356409,Human_RBP_ID_17474056,Human_RBP_ID_18264737,Human_RBP_ID_23577081 RMVar_hsa_circ_269791 40639 RMVar_ID_40639 Human_SNP_ID_510558530 A-to-I Human chr12 - 89427589 89427589 89427589 TCAAGCCATTCTCCAGCCTCAGCCTCCTGAGTAGCTAGAACTACAGGCACACACTAGCATGCCTG TCAAGCCATTCTCCAGCCTCAGCCTCCTGAGTTGCTAGAACTACAGGCACACACTAGCATGCCTG T A POC1B Ensembl:ENSG00000139323 Protein coding exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs112319982 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21837,RMVar_hsa_circ_301195 40640 RMVar_ID_40640 Human_SNP_ID_510558532 A-to-I Human chr12 - 89427601 89427601 89427601 AAACTCTTGGGCTCAAGCCATTCTCCAGCCTCAGCCTCCTGAGTAGCTAGAACTACAGGCACACA AAACTCTTGGGCTCAAGCCATTCTCCAGCCTCGGCCTCCTGAGTAGCTAGAACTACAGGCACACA T C POC1B Ensembl:ENSG00000139323 Protein coding exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1261083505 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21837,RMVar_hsa_circ_301195 40641 RMVar_ID_40641 Human_SNP_ID_510558761 A-to-I Human chr12 - 89428689 89428689 89428689 AGCTGGAGGTGGTGGTGGGCACCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGTG AGCTGGAGGTGGTGGTGGGCACCTGTAGTCCCGGCTACTCGGGAGGCTGAGGCAGGAGAATGGTG T C POC1B Ensembl:ENSG00000139323 Protein coding exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1192893402 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21837,RMVar_hsa_circ_301195 40642 RMVar_ID_40642 Human_SNP_ID_510565279 A-to-I Human chr12 - 89456310 89456310 89456310 CTAATATAAAGAGTTTTAAACTGGTTGGGCACAGTGGCTCACACCTGTAATCCTAGCACTTTGGA CTAATATAAAGAGTTTTAAACTGGTTGGGCACCGTGGCTCACACCTGTAATCCTAGCACTTTGGA T G POC1B Ensembl:ENSG00000139323 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs766586971 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21837,RMVar_hsa_circ_301195 40643 RMVar_ID_40643 Human_SNP_ID_510607456 A-to-I Human chr12 - 89637626 89637626 89637626 GGGAGGCTGAGGTGGGAGGATTGCTTGAGGCCAGGAGTTCGAGGCCAATCTGGGCAATGTGGCGA GGGAGGCTGAGGTGGGAGGATTGCTTGAGGCCTGGAGTTCGAGGCCAATCTGGGCAATGTGGCGA T A ATP2B1 Ensembl:ENSG00000070961 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1339436207 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25008739 RMVar_hsa_circ_11943,RMVar_hsa_circ_58647,RMVar_hsa_circ_306205,RMVar_hsa_circ_47804,RMVar_hsa_circ_158705,RMVar_hsa_circ_268565,RMVar_hsa_circ_57315,RMVar_hsa_circ_158706,RMVar_hsa_circ_342048,RMVar_hsa_circ_357141,RMVar_hsa_circ_158707,RMVar_hsa_circ_61285,RMVar_hsa_circ_62163,RMVar_hsa_circ_298927,RMVar_hsa_circ_158717,RMVar_hsa_circ_54014,RMVar_hsa_circ_52965,RMVar_hsa_circ_300952,RMVar_hsa_circ_158723,RMVar_hsa_circ_334145 40644 RMVar_ID_40644 Human_SNP_ID_510608665 A-to-I Human chr12 - 89642884 89642884 89642884 ATAAGCAGTTCTGGCCAGGCATGGTGGCTCACATTTGTAATCCCAGCACTTTGGGAGGCTGAGGC ATAAGCAGTTCTGGCCAGGCATGGTGGCTCACGTTTGTAATCCCAGCACTTTGGGAGGCTGAGGC T C ATP2B1 Ensembl:ENSG00000070961 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1190040200 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11943,RMVar_hsa_circ_58647,RMVar_hsa_circ_57315,RMVar_hsa_circ_158706,RMVar_hsa_circ_342048,RMVar_hsa_circ_158707,RMVar_hsa_circ_61285,RMVar_hsa_circ_62163,RMVar_hsa_circ_54014,RMVar_hsa_circ_52965,RMVar_hsa_circ_334145,RMVar_hsa_circ_158728,RMVar_hsa_circ_300228 40645 RMVar_ID_40645 Human_SNP_ID_510635609 A-to-I Human chr12 + 89753632 89753632 89753632 CCCTCTAAGAGGCAGATGCAGGTGCTGGAAACATGCATAGCAACAGTAGGCTGAGTATCCAACAC CCCTCTAAGAGGCAGATGCAGGTGCTGGAAACTTGCATAGCAACAGTAGGCTGAGTATCCAACAC A T MRPL2P1,AC009522.1 Ensembl:ENSG00000257480,Ensembl:ENSG00000258216 Pseudogene,lincRNA exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1239833478 Functional Loss SNV dbSNP153 33..33 33 - - - 40646 RMVar_ID_40646 Human_SNP_ID_710482949 A-to-I Human chrX + 15783670 15783670 15783670 AAAATTAGCCAGGCATGGTGGTGAGCACCTGTAATGCCAGCTACTCGGGAAGCTGAGGCTGGAGA AAAATTAGCCAGGCATGGTGGTGAGCACCTGTGATGCCAGCTACTCGGGAAGCTGAGGCTGGAGA A G CA5B Ensembl:ENSG00000169239 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005216447 Functional Loss SNV dbSNP153 33..33 33 - - - 40647 RMVar_ID_40647 Human_SNP_ID_710484369 A-to-I Human chrX + 15791494 15791494 15791494 TACTAGTTATGAAGCTCATTTATTTATTTTTGAGACAGGGTCTTGTTCTGTTGCCCAGGAGGGAT TACTAGTTATGAAGCTCATTTATTTATTTTTGTGACAGGGTCTTGTTCTGTTGCCCAGGAGGGAT A T ZRSR2 Ensembl:ENSG00000169249 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs952130888 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16854294 40648 RMVar_ID_40648 Human_SNP_ID_710484380 A-to-I Human chrX + 15791546 15791546 15791546 GCCCAGGAGGGATGTGCACAACCACGGCTCACAGCAGCCTCCACCTCCCAGGCTCAAGCAGTCCT GCCCAGGAGGGATGTGCACAACCACGGCTCACGGCAGCCTCCACCTCCCAGGCTCAAGCAGTCCT A G ZRSR2 Ensembl:ENSG00000169249 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1289905929 Functional Loss SNV dbSNP153 33..33 33 - - - 40649 RMVar_ID_40649 Human_SNP_ID_710484477 A-to-I Human chrX + 15791998 15791998 15791998 TGGCTAATTTTTAAAATTTTCGTAGAGACGGGATTTCACTGTGTTGCCTGGGCTGGTCTCGAACT TGGCTAATTTTTAAAATTTTCGTAGAGACGGGGTTTCACTGTGTTGCCTGGGCTGGTCTCGAACT A G ZRSR2 Ensembl:ENSG00000169249 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1231646271 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16854297 40650 RMVar_ID_40650 Human_SNP_ID_710492620 A-to-I Human chrX - 15839768 15839768 15839768 TTAAGAATATTTGGGCTGAGCACGGTGGCCCAAGCTTGTAATCCCAGCACTTTGGGAGGCCGGGG TTAAGAATATTTGGGCTGAGCACGGTGGCCCAGGCTTGTAATCCCAGCACTTTGGGAGGCCGGGG T C AP1S2 Ensembl:ENSG00000182287 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1064868 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87985,RMVar_hsa_circ_261426 40651 RMVar_ID_40651 Human_SNP_ID_710493052 A-to-I Human chrX - 15842944 15842944 15842944 TCGGCTCTCTGCAACCTCCGCTTCCTGTGTTCAAGCAATCCTCCTGCCTCAGCCTCCCAAGTAGC TCGGCTCTCTGCAACCTCCGCTTCCTGTGTTCGAGCAATCCTCCTGCCTCAGCCTCCCAAGTAGC T C AP1S2 Ensembl:ENSG00000182287 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs755971183 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87985,RMVar_hsa_circ_261426 40652 RMVar_ID_40652 Human_SNP_ID_710540914 A-to-I Human chrX + 16152891 16152891 16152891 CTTCTGATGTGAAGCAAACCTTCCCTTTTCAGAAAAGGGAACAAGTAGAAAATTATTTTTTAAGC CTTCTGATGTGAAGCAAACCTTCCCTTTTCAGGAAAGGGAACAAGTAGAAAATTATTTTTTAAGC A G GRPR Ensembl:ENSG00000126010 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1016560860 Functional Loss SNV dbSNP153 33..33 33 - - - 40653 RMVar_ID_40653 Human_SNP_ID_710622242 A-to-I Human chrX - 16605665 16605665 16605665 CAGGCTGGAGTGCAATCATGTGGTCTTGGCTCACTGCAACCTCCACCTCCCGGGTTCAAGCAATT CAGGCTGGAGTGCAATCATGTGGTCTTGGCTCGCTGCAACCTCCACCTCCCGGGTTCAAGCAATT T C CTPS2 Ensembl:ENSG00000047230 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1013124247 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8716012 RMVar_hsa_circ_5715,RMVar_hsa_circ_98982,RMVar_hsa_circ_120103,RMVar_hsa_circ_104891,RMVar_hsa_circ_261438,RMVar_hsa_circ_76837,RMVar_hsa_circ_261439,RMVar_hsa_circ_261440,RMVar_hsa_circ_261437,RMVar_hsa_circ_33164 40654 RMVar_ID_40654 Human_SNP_ID_710640469 A-to-I Human chrX - 16709676 16709676 16709676 CCTGGCTAATTTTTGTATTTTTAGTAGAGACAAGGTTTAACCATGTTGGCCAGGATGGTCTTGAT CCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTAACCATGTTGGCCAGGATGGTCTTGAT T C CTPS2 Ensembl:ENSG00000047230 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1257746465 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104891,RMVar_hsa_circ_261440,RMVar_hsa_circ_117555,RMVar_hsa_circ_261469 40655 RMVar_ID_40655 Human_SNP_ID_710640470 A-to-I Human chrX - 16709677 16709677 16709677 GCCTGGCTAATTTTTGTATTTTTAGTAGAGACAAGGTTTAACCATGTTGGCCAGGATGGTCTTGA GCCTGGCTAATTTTTGTATTTTTAGTAGAGACGAGGTTTAACCATGTTGGCCAGGATGGTCTTGA T C CTPS2 Ensembl:ENSG00000047230 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1325755197 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104891,RMVar_hsa_circ_261440,RMVar_hsa_circ_117555,RMVar_hsa_circ_261469 40656 RMVar_ID_40656 Human_SNP_ID_710642800 A-to-I Human chrX + 16721344 16721344 16721344 ACCTCCACCTCCAGGGTTCAAGTGATCTTCCTACCTTATCCTCTCCAGTAGCTTGGATTACAGGC ACCTCCACCTCCAGGGTTCAAGTGATCTTCCTGCCTTATCCTCTCCAGTAGCTTGGATTACAGGC A G SYAP1 Ensembl:ENSG00000169895 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1287301258 Functional Loss SNV dbSNP153 33..33 33 - - - 40657 RMVar_ID_40657 Human_SNP_ID_710646361 A-to-I Human chrX + 16742213 16742213 16742213 TCGCTCTGTCACCCAGCCTGGAGCGCAGTGGCACGATCTCGGCTCACTGCAACCTTCTCCTCCCA TCGCTCTGTCACCCAGCCTGGAGCGCAGTGGCTCGATCTCGGCTCACTGCAACCTTCTCCTCCCA A T SYAP1 Ensembl:ENSG00000169895 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973741866 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92894,RMVar_hsa_circ_342425,RMVar_hsa_circ_328820,RMVar_hsa_circ_261475,RMVar_hsa_circ_261471,RMVar_hsa_circ_261470,RMVar_hsa_circ_68484,RMVar_hsa_circ_300386,RMVar_hsa_circ_334167,RMVar_hsa_circ_261474,RMVar_hsa_circ_278376 40658 RMVar_ID_40658 Human_SNP_ID_710648671 A-to-I Human chrX + 16754607 16754607 16754607 AAAATTAGCTGTGCATGGTGGCGGGCACCTATAATCCCAGCAACTCGGGAGGCTGAGGCAAGAGA AAAATTAGCTGTGCATGGTGGCGGGCACCTATGATCCCAGCAACTCGGGAGGCTGAGGCAAGAGA A G SYAP1 Ensembl:ENSG00000169895 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs977266807 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26266543 RMVar_hsa_circ_92894,RMVar_hsa_circ_342425,RMVar_hsa_circ_261470,RMVar_hsa_circ_68484,RMVar_hsa_circ_334167 40659 RMVar_ID_40659 Human_SNP_ID_710649821 A-to-I Human chrX + 16761176 16761176 16761176 GAGGTTGCAGCGAGCTGAGATCGCGCCACTGCACTCCAGCCTGGGTGATAGAGTGAGATTCAGTC GAGGTTGCAGCGAGCTGAGATCGCGCCACTGCGCTCCAGCCTGGGTGATAGAGTGAGATTCAGTC A G SYAP1 Ensembl:ENSG00000169895 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017384348 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_97397,Human_miRNA_ID_215215,Human_miRNA_ID_224755,Human_miRNA_ID_763264,Human_miRNA_ID_768157,Human_miRNA_ID_1073975,Human_miRNA_ID_1327750 40660 RMVar_ID_40660 Human_SNP_ID_710650148 A-to-I Human chrX + 16763143 16763142 16763143 GACCCCTGCCTCTACAAAAATACAAATGAGCCAGGTGTGGTAGCCCACACCTGTGGTCCTAGCTA GACCCCTGCCTCTACAAAAATACAAATGAGCC_GGTGTGGTAGCCCACACCTGTGGTCCTAGCTA CA C SYAP1 Ensembl:ENSG00000169895 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1314204526 Functional Loss DEL dbSNP153 33..33 33 - - - 40661 RMVar_ID_40661 Human_SNP_ID_710650152 A-to-I Human chrX + 16763188 16763188 16763188 CACACCTGTGGTCCTAGCTACTTGGAAGGCTGAGGCAGGAGGATCGCTTGAGCCCAGGAGATCCA CACACCTGTGGTCCTAGCTACTTGGAAGGCTGCGGCAGGAGGATCGCTTGAGCCCAGGAGATCCA A C SYAP1 Ensembl:ENSG00000169895 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1171725827 Functional Loss SNV dbSNP153 33..33 33 - - - 40662 RMVar_ID_40662 Human_SNP_ID_710650160 A-to-I Human chrX + 16763268 16763268 16763268 TGATCATGCCACTGCACTTCAGCCTGGGTGACAGAGACTCTGTTTCAAAAAAGGGAGGGGGGGCA TGATCATGCCACTGCACTTCAGCCTGGGTGACGGAGACTCTGTTTCAAAAAAGGGAGGGGGGGCA A G SYAP1 Ensembl:ENSG00000169895 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1243269683 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7989417 40663 RMVar_ID_40663 Human_SNP_ID_710650203 A-to-I Human chrX + 16763452 16763452 16763452 TCAGCTCACGGCAACCTCCGCCTCCCAAGTTCAAGCGATTCTCCCACCTCAGCCTCCAGAGTAGC TCAGCTCACGGCAACCTCCGCCTCCCAAGTTCGAGCGATTCTCCCACCTCAGCCTCCAGAGTAGC A G SYAP1 Ensembl:ENSG00000169895 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs919896053 Functional Loss SNV dbSNP153 33..33 33 - - - 40664 RMVar_ID_40664 Human_SNP_ID_710650230 A-to-I Human chrX + 16763538 16763538 16763538 CCATGCCCAGCTAATTTTTTTGTATTTTTAGCAGAGATGGGGTTTCACCGTGTTGGCCAGGCTGG CCATGCCCAGCTAATTTTTTTGTATTTTTAGCGGAGATGGGGTTTCACCGTGTTGGCCAGGCTGG A G SYAP1 Ensembl:ENSG00000169895 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1309931656 Functional Loss SNV dbSNP153 33..33 33 - - - 40665 RMVar_ID_40665 Human_SNP_ID_710650313 A-to-I Human chrX + 16763943 16763943 16763943 TTGCCTGGGCTGGAATGCAATGGCGCAGTCTCAGCTCACTGCAAACCTCCGGCTCCCGGGTTCAG TTGCCTGGGCTGGAATGCAATGGCGCAGTCTCGGCTCACTGCAAACCTCCGGCTCCCGGGTTCAG A G SYAP1 Ensembl:ENSG00000169895 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1211602724 Functional Loss SNV dbSNP153 33..33 33 - - - 40666 RMVar_ID_40666 Human_SNP_ID_710650314 A-to-I Human chrX + 16763953 16763953 16763953 TGGAATGCAATGGCGCAGTCTCAGCTCACTGCAAACCTCCGGCTCCCGGGTTCAGGCAGTTCTCC TGGAATGCAATGGCGCAGTCTCAGCTCACTGCGAACCTCCGGCTCCCGGGTTCAGGCAGTTCTCC A G SYAP1 Ensembl:ENSG00000169895 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1467864721 Functional Loss SNV dbSNP153 33..33 33 - - - 40667 RMVar_ID_40667 Human_SNP_ID_710650469 A-to-I Human chrX + 16764596 16764596 16764596 GTTGGCCAGGCTGGTCTTGAACGACTGGCCTCAGGTGATCCGCCCACCTCGGCCTCTCAAAGTGC GTTGGCCAGGCTGGTCTTGAACGACTGGCCTCGGGTGATCCGCCCACCTCGGCCTCTCAAAGTGC A G SYAP1 Ensembl:ENSG00000169895 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1191131908 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16856092 40668 RMVar_ID_40668 Human_SNP_ID_710650496 A-to-I Human chrX + 16764743 16764743 16764743 TTGAGACAGGGTCTTGCTCTGTCACTCAGGCTAGAGTGCAGTGGTGGGATCTCAGCTCACTGCAG TTGAGACAGGGTCTTGCTCTGTCACTCAGGCTGGAGTGCAGTGGTGGGATCTCAGCTCACTGCAG A G SYAP1 Ensembl:ENSG00000169895 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs928498174 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8226688 40669 RMVar_ID_40669 Human_SNP_ID_710650535 A-to-I Human chrX + 16764970 16764970 16764970 TATCTGCCTCGGCCTTCCAAAGTGCTGGGATTACAGGCATGATGAGCCACTGCACCTGGCCAAAA TATCTGCCTCGGCCTTCCAAAGTGCTGGGATTCCAGGCATGATGAGCCACTGCACCTGGCCAAAA A C SYAP1 Ensembl:ENSG00000169895 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1002797535 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23202781 40670 RMVar_ID_40670 Human_SNP_ID_710655656 A-to-I Human chrX + 16790430 16790430 16790430 TGCTATGTTGCCCAGGCTGGTCTTGAACTCCTAGGCTCAGGCGATCGTTCTGCCTTGGCCTCCCA TGCTATGTTGCCCAGGCTGGTCTTGAACTCCTGGGCTCAGGCGATCGTTCTGCCTTGGCCTCCCA A G TXLNG Ensembl:ENSG00000086712 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264865916 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26266605 40671 RMVar_ID_40671 Human_SNP_ID_710656214 A-to-I Human chrX + 16793723 16793723 16793723 GCCCAGGCTGGAGTGTAGTTAACGCTTATTGCAGCCTTGAACTCCTGGTCTCAAGTGATCTTCCT GCCCAGGCTGGAGTGTAGTTAACGCTTATTGCCGCCTTGAACTCCTGGTCTCAAGTGATCTTCCT A C TXLNG Ensembl:ENSG00000086712 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1387480846 Functional Loss SNV dbSNP153 33..33 33 - - - 40672 RMVar_ID_40672 Human_SNP_ID_710669194 A-to-I Human chrX - 16860611 16860611 16860611 GGAGTGCAGTGGTGTGACCTCAGCTCACTGCAACCTCTGCCTCCTGGGTTCAAGCGATTTCCCGA GGAGTGCAGTGGTGTGACCTCAGCTCACTGCAGCCTCTGCCTCCTGGGTTCAAGCGATTTCCCGA T C RBBP7 Ensembl:ENSG00000102054 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1214717183 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19084,RMVar_hsa_circ_22147,RMVar_hsa_circ_359994,RMVar_hsa_circ_366930,RMVar_hsa_circ_261482,RMVar_hsa_circ_66127,RMVar_hsa_circ_10463,RMVar_hsa_circ_284041,RMVar_hsa_circ_97536,RMVar_hsa_circ_261485,RMVar_hsa_circ_261486 40673 RMVar_ID_40673 Human_SNP_ID_710755783 A-to-I Human chrX + 17380486 17380486 17380486 CCCAGGCTCCCATCTCGGCCCCCCAAGTAGCTAGGACTACAGGTGTGCACCACTACGCTAGGCTA CCCAGGCTCCCATCTCGGCCCCCCAAGTAGCTGGGACTACAGGTGTGCACCACTACGCTAGGCTA A G NHS Ensembl:ENSG00000188158 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1280039348 Functional Loss SNV dbSNP153 33..33 33 - - - 40674 RMVar_ID_40674 Human_SNP_ID_710944161 A-to-I Human chrX + 18514982 18514982 18514982 CAACATGCCCGGCTAATTTTTGTATTTTCAGTAGAGACGGGGCTTCATTACGTTGGCCAGGCTGG CAACATGCCCGGCTAATTTTTGTATTTTCAGTGGAGACGGGGCTTCATTACGTTGGCCAGGCTGG A G CDKL5 Ensembl:ENSG00000008086 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs780413325 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59601,RMVar_hsa_circ_287460,RMVar_hsa_circ_349355,RMVar_hsa_circ_368781,RMVar_hsa_circ_329203,RMVar_hsa_circ_295261,RMVar_hsa_circ_7922,RMVar_hsa_circ_58512,RMVar_hsa_circ_261534,RMVar_hsa_circ_261535,RMVar_hsa_circ_261536,RMVar_hsa_circ_261533 40675 RMVar_ID_40675 Human_SNP_ID_711015946 A-to-I Human chrX - 18915267 18915267 18915267 ATGATCATGGCTCACTGCAGCCTTCACCTCCCAGGCCCAAGCGATCCCCCTACCTCAACCTCCCA ATGATCATGGCTCACTGCAGCCTTCACCTCCCGGGCCCAAGCGATCCCCCTACCTCAACCTCCCA T C PHKA2,RN7SL48P Ensembl:ENSG00000044446,Ensembl:ENSG00000266710 Protein coding,Other intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1196694859 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122671,RMVar_hsa_circ_346692,RMVar_hsa_circ_127097,RMVar_hsa_circ_371703,RMVar_hsa_circ_374286,RMVar_hsa_circ_110365,RMVar_hsa_circ_115052,RMVar_hsa_circ_118797,RMVar_hsa_circ_104511,RMVar_hsa_circ_261565,RMVar_hsa_circ_261573,RMVar_hsa_circ_92855,RMVar_hsa_circ_95056,RMVar_hsa_circ_90555,RMVar_hsa_circ_81116,RMVar_hsa_circ_261569,RMVar_hsa_circ_261571,RMVar_hsa_circ_261572,RMVar_hsa_circ_261570,RMVar_hsa_circ_261567,RMVar_hsa_circ_261568,RMVar_hsa_circ_261566,RMVar_hsa_circ_261563,RMVar_hsa_circ_261564,RMVar_hsa_circ_261562,RMVar_hsa_circ_103900,RMVar_hsa_circ_368872,RMVar_hsa_circ_15367,RMVar_hsa_circ_33157,RMVar_hsa_circ_290903,RMVar_hsa_circ_360099,RMVar_hsa_circ_261584,RMVar_hsa_circ_53800,RMVar_hsa_circ_52615,RMVar_hsa_circ_72504,RMVar_hsa_circ_277845,RMVar_hsa_circ_261585 40676 RMVar_ID_40676 Human_SNP_ID_711017092 A-to-I Human chrX - 18921390 18921390 18921390 TGAGACGGAGTCTCTGTCGCCCAGGCTGGAGTACAGTGGCGCGATCTCGGCTCACTGCAACCTCC TGAGACGGAGTCTCTGTCGCCCAGGCTGGAGTTCAGTGGCGCGATCTCGGCTCACTGCAACCTCC T A PHKA2 Ensembl:ENSG00000044446 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1478023311 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122671,RMVar_hsa_circ_346692,RMVar_hsa_circ_127097,RMVar_hsa_circ_374286,RMVar_hsa_circ_110365,RMVar_hsa_circ_115052,RMVar_hsa_circ_118797,RMVar_hsa_circ_104511,RMVar_hsa_circ_261565,RMVar_hsa_circ_92855,RMVar_hsa_circ_95056,RMVar_hsa_circ_90555,RMVar_hsa_circ_261569,RMVar_hsa_circ_261571,RMVar_hsa_circ_261570,RMVar_hsa_circ_261567,RMVar_hsa_circ_261568,RMVar_hsa_circ_261566,RMVar_hsa_circ_261563,RMVar_hsa_circ_261564,RMVar_hsa_circ_261562,RMVar_hsa_circ_368872,RMVar_hsa_circ_33157,RMVar_hsa_circ_53800,RMVar_hsa_circ_52615,RMVar_hsa_circ_55649,RMVar_hsa_circ_72504,RMVar_hsa_circ_277845,RMVar_hsa_circ_261585,RMVar_hsa_circ_334575,RMVar_hsa_circ_261587,RMVar_hsa_circ_261586,RMVar_hsa_circ_336719 40677 RMVar_ID_40677 Human_SNP_ID_711017093 A-to-I Human chrX - 18921390 18921390 18921390 TGAGACGGAGTCTCTGTCGCCCAGGCTGGAGTACAGTGGCGCGATCTCGGCTCACTGCAACCTCC TGAGACGGAGTCTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCGATCTCGGCTCACTGCAACCTCC T C PHKA2 Ensembl:ENSG00000044446 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1478023311 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122671,RMVar_hsa_circ_346692,RMVar_hsa_circ_127097,RMVar_hsa_circ_374286,RMVar_hsa_circ_110365,RMVar_hsa_circ_115052,RMVar_hsa_circ_118797,RMVar_hsa_circ_104511,RMVar_hsa_circ_261565,RMVar_hsa_circ_92855,RMVar_hsa_circ_95056,RMVar_hsa_circ_90555,RMVar_hsa_circ_261569,RMVar_hsa_circ_261571,RMVar_hsa_circ_261570,RMVar_hsa_circ_261567,RMVar_hsa_circ_261568,RMVar_hsa_circ_261566,RMVar_hsa_circ_261563,RMVar_hsa_circ_261564,RMVar_hsa_circ_261562,RMVar_hsa_circ_368872,RMVar_hsa_circ_33157,RMVar_hsa_circ_53800,RMVar_hsa_circ_52615,RMVar_hsa_circ_55649,RMVar_hsa_circ_72504,RMVar_hsa_circ_277845,RMVar_hsa_circ_261585,RMVar_hsa_circ_334575,RMVar_hsa_circ_261587,RMVar_hsa_circ_261586,RMVar_hsa_circ_336719 40678 RMVar_ID_40678 Human_SNP_ID_711131211 A-to-I Human chrX - 19538329 19538329 19538329 ATGGTGGTGTGCGCTTGTAGTCCTAGCTACTCAGGAGGCTGAGGCAGGAGGATCGCTTGAGTTTG ATGGTGGTGTGCGCTTGTAGTCCTAGCTACTCGGGAGGCTGAGGCAGGAGGATCGCTTGAGTTTG T C SH3KBP1 Ensembl:ENSG00000147010 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1370183869 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50502,RMVar_hsa_circ_377827 40679 RMVar_ID_40679 Human_SNP_ID_711166671 A-to-I Human chrX - 19743211 19743211 19743211 GTAGAGCTGGGGTTTTGCCATGTTGCCTAGCTAGTCTTGAACGCCTGGGCTCAAGCAAGCCTCCT GTAGAGCTGGGGTTTTGCCATGTTGCCTAGCTTGTCTTGAACGCCTGGGCTCAAGCAAGCCTCCT T A SH3KBP1 Ensembl:ENSG00000147010 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs765367450 Functional Loss SNV dbSNP153 33..33 33 - - - 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_310490,RMVar_hsa_circ_261628,RMVar_hsa_circ_337027,RMVar_hsa_circ_291076,RMVar_hsa_circ_296730,RMVar_hsa_circ_340273 40680 RMVar_ID_40680 Human_SNP_ID_711172649 A-to-I Human chrX - 19776672 19776672 19776672 ATGGTGGTGTGCGCTTGTGGTCCCAGTTACTCAGTAGGCTGAGGTGGGAGGATCACTTGAGCCCA ATGGTGGTGTGCGCTTGTGGTCCCAGTTACTCGGTAGGCTGAGGTGGGAGGATCACTTGAGCCCA T C SH3KBP1 Ensembl:ENSG00000147010 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1346916531 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 40681 RMVar_ID_40681 Human_SNP_ID_711172670 A-to-I Human chrX - 19776791 19776791 19776791 CTGGTGCTTTGGGAGGCTGAGGCAGGAGGATCACTTGAGGCCAGGAGTTTGAGACCATCCTGGGA CTGGTGCTTTGGGAGGCTGAGGCAGGAGGATCTCTTGAGGCCAGGAGTTTGAGACCATCCTGGGA T A SH3KBP1 Ensembl:ENSG00000147010 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs764555106 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 40682 RMVar_ID_40682 Human_SNP_ID_711177166 A-to-I Human chrX - 19803378 19803378 19803378 TAGCGAGACCTTGTCTCTACACTAAATTTAAAAATTAGCCAGGCATGGTGGTGTGTGCCTGGCTT TAGCGAGACCTTGTCTCTACACTAAATTTAAATATTAGCCAGGCATGGTGGTGTGTGCCTGGCTT T A SH3KBP1 Ensembl:ENSG00000147010 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1344060328 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 40683 RMVar_ID_40683 Human_SNP_ID_711198831 A-to-I Human chrX - 19928545 19928545 19928545 GAGTTTTGCTCTTATTCCCCAGGCTGGAGTACAATGGCACGATCTCAGCTCAGTGCAACCTCCGC GAGTTTTGCTCTTATTCCCCAGGCTGGAGTACGATGGCACGATCTCAGCTCAGTGCAACCTCCGC T C BCLAF3 Ensembl:ENSG00000173681 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1379267235 Functional Loss SNV dbSNP153 33..33 33 - - - 40684 RMVar_ID_40684 Human_SNP_ID_711199087 A-to-I Human chrX - 19930119 19930119 19930119 TTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAAGCGATC TTTAGTAGAGACGGGGTTTCACCATGTTGGCCGGGCTGGTCTCGAACTCCTGACCTCAAGCGATC T C BCLAF3 Ensembl:ENSG00000173681 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs760702196 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_261636,RMVar_hsa_circ_9590,RMVar_hsa_circ_291158,RMVar_hsa_circ_305634,RMVar_hsa_circ_314769,RMVar_hsa_circ_299094,RMVar_hsa_circ_45802,RMVar_hsa_circ_48722,RMVar_hsa_circ_22872,RMVar_hsa_circ_261638,RMVar_hsa_circ_261639,RMVar_hsa_circ_261640,RMVar_hsa_circ_261637,RMVar_hsa_circ_261635 40685 RMVar_ID_40685 Human_SNP_ID_711199735 A-to-I Human chrX - 19933878 19933878 19933878 TAGTCCCAGCTACTCAGGAGGCTGAGGTGGGAAGATCGCTTCAGCCTGGGAGGCAGAGGTTGCAG TAGTCCCAGCTACTCAGGAGGCTGAGGTGGGAGGATCGCTTCAGCCTGGGAGGCAGAGGTTGCAG T C BCLAF3 Ensembl:ENSG00000173681 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs926346854 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_261636,RMVar_hsa_circ_9590,RMVar_hsa_circ_291158,RMVar_hsa_circ_305634,RMVar_hsa_circ_314769,RMVar_hsa_circ_299094,RMVar_hsa_circ_45802,RMVar_hsa_circ_48722,RMVar_hsa_circ_22872,RMVar_hsa_circ_261638,RMVar_hsa_circ_261639,RMVar_hsa_circ_261640,RMVar_hsa_circ_261637,RMVar_hsa_circ_261635 40686 RMVar_ID_40686 Human_SNP_ID_711203120 A-to-I Human chrX - 19951413 19951413 19951413 TTTTGTATTTTTGGTGGAGATGGGGTTTTACTATGTTGGCCAGGCTGGTCTTGAACTCCTGTTCA TTTTGTATTTTTGGTGGAGATGGGGTTTTACTTTGTTGGCCAGGCTGGTCTTGAACTCCTGTTCA T A BCLAF3 Ensembl:ENSG00000173681 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924737687 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_261636,RMVar_hsa_circ_9590,RMVar_hsa_circ_291158,RMVar_hsa_circ_299094,RMVar_hsa_circ_45802,RMVar_hsa_circ_48722,RMVar_hsa_circ_261641,RMVar_hsa_circ_16945,RMVar_hsa_circ_301940,RMVar_hsa_circ_261635,RMVar_hsa_circ_271810,RMVar_hsa_circ_261642,RMVar_hsa_circ_274628,RMVar_hsa_circ_261643,RMVar_hsa_circ_33837,RMVar_hsa_circ_271162,RMVar_hsa_circ_293965,RMVar_hsa_circ_317404,RMVar_hsa_circ_261645,RMVar_hsa_circ_261646,RMVar_hsa_circ_261644 40687 RMVar_ID_40687 Human_SNP_ID_711203121 A-to-I Human chrX - 19951413 19951413 19951413 TTTTGTATTTTTGGTGGAGATGGGGTTTTACTATGTTGGCCAGGCTGGTCTTGAACTCCTGTTCA TTTTGTATTTTTGGTGGAGATGGGGTTTTACTGTGTTGGCCAGGCTGGTCTTGAACTCCTGTTCA T C BCLAF3 Ensembl:ENSG00000173681 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924737687 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_261636,RMVar_hsa_circ_9590,RMVar_hsa_circ_291158,RMVar_hsa_circ_299094,RMVar_hsa_circ_45802,RMVar_hsa_circ_48722,RMVar_hsa_circ_261641,RMVar_hsa_circ_16945,RMVar_hsa_circ_301940,RMVar_hsa_circ_261635,RMVar_hsa_circ_271810,RMVar_hsa_circ_261642,RMVar_hsa_circ_274628,RMVar_hsa_circ_261643,RMVar_hsa_circ_33837,RMVar_hsa_circ_271162,RMVar_hsa_circ_293965,RMVar_hsa_circ_317404,RMVar_hsa_circ_261645,RMVar_hsa_circ_261646,RMVar_hsa_circ_261644 40688 RMVar_ID_40688 Human_SNP_ID_711204784 A-to-I Human chrX - 19962216 19962216 19962216 GTTTGTGCCACTGCACTCCAGCCTGGGTGACAAAGCGAGACCCTGTCTCAAAAATAAAAACTAAA GTTTGTGCCACTGCACTCCAGCCTGGGTGACAGAGCGAGACCCTGTCTCAAAAATAAAAACTAAA T C BCLAF3 Ensembl:ENSG00000173681 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs919170142 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_261636,RMVar_hsa_circ_9590,RMVar_hsa_circ_291158,RMVar_hsa_circ_45802,RMVar_hsa_circ_16945,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_293965,RMVar_hsa_circ_261646,RMVar_hsa_circ_328252,RMVar_hsa_circ_261648,RMVar_hsa_circ_340708 40689 RMVar_ID_40689 Human_SNP_ID_711204794 A-to-I Human chrX - 19962322 19962322 19962322 CAAAAATTAGCTGGGTGTGTTGACATGTGCCTATAGTCCCAGCTACTTGGGAGGCTGGGGTGGGA CAAAAATTAGCTGGGTGTGTTGACATGTGCCTGTAGTCCCAGCTACTTGGGAGGCTGGGGTGGGA T C BCLAF3 Ensembl:ENSG00000173681 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs887594951 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_261636,RMVar_hsa_circ_9590,RMVar_hsa_circ_291158,RMVar_hsa_circ_45802,RMVar_hsa_circ_16945,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_293965,RMVar_hsa_circ_261646,RMVar_hsa_circ_328252,RMVar_hsa_circ_261648,RMVar_hsa_circ_340708 40690 RMVar_ID_40690 Human_SNP_ID_711208917 A-to-I Human chrX - 19985499 19985499 19985499 TCACTGTAGCCTTGAATTCCTGGGCTTTAGCAATCCCCCTGCCTCAACCTCCCGAGAAGCTAGGA TCACTGTAGCCTTGAATTCCTGGGCTTTAGCAGTCCCCCTGCCTCAACCTCCCGAGAAGCTAGGA T C LOC729609,RF00017-4520 RNACentral:URS00009B745B,RNACentral:URS000099C2D3 lincRNA,SRP RNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs760996182 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7991758 40691 RMVar_ID_40691 Human_SNP_ID_711530631 A-to-I Human chrX + 21845231 21845231 21845231 ATTGCCATGTTTAGCTCATTTTTTCTCCTTGGAAAAACGCTGATGCAGACTTTGGCACAAATGAT ATTGCCATGTTTAGCTCATTTTTTCTCCTTGGGAAAACGCTGATGCAGACTTTGGCACAAATGAT A G MBTPS2 Ensembl:ENSG00000012174 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1318202719 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_733152,Human_RBP_ID_1230206,Human_RBP_ID_9245549,Human_RBP_ID_16863284,Human_RBP_ID_21765362 Human_Splice_Rec_2192278,Human_Splice_Rec_2192298,Human_Splice_Rec_2192308 RMVar_hsa_circ_107407,RMVar_hsa_circ_328322,RMVar_hsa_circ_261718 40692 RMVar_ID_40692 Human_SNP_ID_711548788 A-to-I Human chrX + 21945884 21945884 21945884 TGACCTCATGATCCACCCGCATTGGCCTCTCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCGC TGACCTCATGATCCACCCGCATTGGCCTCTCACAGTGCTGGGATTACAGGTGTGAGCCACCGCGC A C SMS Ensembl:ENSG00000102172 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1569340148 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104311,RMVar_hsa_circ_261729 40693 RMVar_ID_40693 Human_SNP_ID_711879260 A-to-I Human chrX + 23669025 23669025 23669025 TCGGCTCACTGCAACCTCCGCCGCCCGGGTTCAAGCGATTCTTCTGCCTCAGCCTCCCAGGTAGC TCGGCTCACTGCAACCTCCGCCGCCCGGGTTCGAGCGATTCTTCTGCCTCAGCCTCCCAGGTAGC A G PRDX4 Ensembl:ENSG00000123131 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1463412079 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102679,RMVar_hsa_circ_261762 40694 RMVar_ID_40694 Human_SNP_ID_711885705 A-to-I Human chrX - 23701671 23701670 23701672 GGAGGATCGCTTGAGACCAGCCTGGGAAACATAGTGAGACCCTTTCTCTACAAAAAGTTAAAAAA GGAGGATCGCTTGAGACCAGCCTGGGAAACA__GTGAGACCCTTTCTCTACAAAAAGTTAAAAAA CTA C ACOT9 Ensembl:ENSG00000123130 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1358938351 Functional Loss DEL dbSNP153 32..33 33 - - - 40695 RMVar_ID_40695 Human_SNP_ID_711885724 A-to-I Human chrX - 23701756 23701756 23701756 GGAAAGCATTTTTAACAAAAAATTTTTAGGCCAGGCACAGTGGTGGCTCATGCCTGTAATCCCAG GGAAAGCATTTTTAACAAAAAATTTTTAGGCCGGGCACAGTGGTGGCTCATGCCTGTAATCCCAG T C ACOT9 Ensembl:ENSG00000123130 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1161106574 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16864062,Human_RBP_ID_18149170 40696 RMVar_ID_40696 Human_SNP_ID_711885780 A-to-I Human chrX - 23702067 23702064 23702068 AGTATTTTTGTGTGTGTGTGTGTGTGTGAGACAGAGTTTCACTCTGTCGCTCCAGCTGGAGTGCA AGTATTTTTGTGTGTGTGTGTGTGTGTGAGA____GTTTCACTCTGTCGCTCCAGCTGGAGTGCA CTCTG C ACOT9 Ensembl:ENSG00000123130 Protein coding 3'UTR GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 29129909,30559470 RNA-Seq:(High) rs1189311300 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_24338087 40697 RMVar_ID_40697 Human_SNP_ID_711888964 A-to-I Human chrX - 23719087 23719087 23719087 TTTTGTATTTTTAGTAGAGACGGGGTTTTACCATGTTGCCCAGGCTGGTCTTGAACTCTTGGACT TTTTGTATTTTTAGTAGAGACGGGGTTTTACCGTGTTGCCCAGGCTGGTCTTGAACTCTTGGACT T C ACOT9 Ensembl:ENSG00000123130 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350247655 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64744,RMVar_hsa_circ_117687,RMVar_hsa_circ_261772,RMVar_hsa_circ_57868,RMVar_hsa_circ_261771,RMVar_hsa_circ_298964,RMVar_hsa_circ_346503,RMVar_hsa_circ_348332,RMVar_hsa_circ_316272,RMVar_hsa_circ_261773 40698 RMVar_ID_40698 Human_SNP_ID_711890120 A-to-I Human chrX - 23724815 23724815 23724815 CTTCTGCCTCAGCCTCCTGAGTAGCTGGGACTATAGGCACACTGCACCATGCCTGGCTAATTTGT CTTCTGCCTCAGCCTCCTGAGTAGCTGGGACTGTAGGCACACTGCACCATGCCTGGCTAATTTGT T C ACOT9 Ensembl:ENSG00000123130 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1238840464 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41837,RMVar_hsa_circ_64744,RMVar_hsa_circ_57868,RMVar_hsa_circ_346503,RMVar_hsa_circ_348332,RMVar_hsa_circ_316272,RMVar_hsa_circ_261773,RMVar_hsa_circ_319050,RMVar_hsa_circ_328937,RMVar_hsa_circ_272163,RMVar_hsa_circ_72178,RMVar_hsa_circ_261775,RMVar_hsa_circ_261776 40699 RMVar_ID_40699 Human_SNP_ID_711890122 A-to-I Human chrX - 23724837 23724837 23724837 AAACTTGCGGGCTCAAGTGTTCCTTCTGCCTCAGCCTCCTGAGTAGCTGGGACTATAGGCACACT AAACTTGCGGGCTCAAGTGTTCCTTCTGCCTCTGCCTCCTGAGTAGCTGGGACTATAGGCACACT T A ACOT9 Ensembl:ENSG00000123130 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1485147758 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41837,RMVar_hsa_circ_64744,RMVar_hsa_circ_57868,RMVar_hsa_circ_346503,RMVar_hsa_circ_348332,RMVar_hsa_circ_316272,RMVar_hsa_circ_261773,RMVar_hsa_circ_319050,RMVar_hsa_circ_328937,RMVar_hsa_circ_272163,RMVar_hsa_circ_72178,RMVar_hsa_circ_261775,RMVar_hsa_circ_261776 40700 RMVar_ID_40700 Human_SNP_ID_711890133 A-to-I Human chrX - 23724874 23724874 23724874 GTAGTGCAGTGGTAAAATCATAGCCTACTGCAACCTTAAACTTGCGGGCTCAAGTGTTCCTTCTG GTAGTGCAGTGGTAAAATCATAGCCTACTGCAGCCTTAAACTTGCGGGCTCAAGTGTTCCTTCTG T C ACOT9 Ensembl:ENSG00000123130 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs745847103 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41837,RMVar_hsa_circ_64744,RMVar_hsa_circ_57868,RMVar_hsa_circ_346503,RMVar_hsa_circ_348332,RMVar_hsa_circ_316272,RMVar_hsa_circ_261773,RMVar_hsa_circ_319050,RMVar_hsa_circ_328937,RMVar_hsa_circ_272163,RMVar_hsa_circ_72178,RMVar_hsa_circ_261775,RMVar_hsa_circ_261776 40701 RMVar_ID_40701 Human_SNP_ID_711890134 A-to-I Human chrX - 23724874 23724874 23724874 GTAGTGCAGTGGTAAAATCATAGCCTACTGCAACCTTAAACTTGCGGGCTCAAGTGTTCCTTCTG GTAGTGCAGTGGTAAAATCATAGCCTACTGCACCCTTAAACTTGCGGGCTCAAGTGTTCCTTCTG T G ACOT9 Ensembl:ENSG00000123130 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs745847103 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41837,RMVar_hsa_circ_64744,RMVar_hsa_circ_57868,RMVar_hsa_circ_346503,RMVar_hsa_circ_348332,RMVar_hsa_circ_316272,RMVar_hsa_circ_261773,RMVar_hsa_circ_319050,RMVar_hsa_circ_328937,RMVar_hsa_circ_272163,RMVar_hsa_circ_72178,RMVar_hsa_circ_261775,RMVar_hsa_circ_261776 40702 RMVar_ID_40702 Human_SNP_ID_711890633 A-to-I Human chrX - 23727524 23727523 23727525 GGCCAAGACTTTGAGACCAGCCTGGGAAACATAGTGAGTCCCCATCTCTACAAAACCCAAAAAAT GGCCAAGACTTTGAGACCAGCCTGGGAAACA__GTGAGTCCCCATCTCTACAAAACCCAAAAAAT CTA C ACOT9 Ensembl:ENSG00000123130 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1195923009 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_41837,RMVar_hsa_circ_64744,RMVar_hsa_circ_57868,RMVar_hsa_circ_346503,RMVar_hsa_circ_348332,RMVar_hsa_circ_316272,RMVar_hsa_circ_261773,RMVar_hsa_circ_319050,RMVar_hsa_circ_328937,RMVar_hsa_circ_272163,RMVar_hsa_circ_72178,RMVar_hsa_circ_261775,RMVar_hsa_circ_261776 40703 RMVar_ID_40703 Human_SNP_ID_711891054 A-to-I Human chrX - 23729906 23729906 23729906 TTTTCTGTGGCCAGGCGCGGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCTGAGGCAGGC TTTTCTGTGGCCAGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGC T C ACOT9 Ensembl:ENSG00000123130 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1461002011 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_186517 RMVar_hsa_circ_41837,RMVar_hsa_circ_64744,RMVar_hsa_circ_57868,RMVar_hsa_circ_346503,RMVar_hsa_circ_348332,RMVar_hsa_circ_316272,RMVar_hsa_circ_261773,RMVar_hsa_circ_319050,RMVar_hsa_circ_328937,RMVar_hsa_circ_272163,RMVar_hsa_circ_72178,RMVar_hsa_circ_261775,RMVar_hsa_circ_261776 40704 RMVar_ID_40704 Human_SNP_ID_711895731 A-to-I Human chrX - 23754117 23754117 23754117 AAAGTGGGACTAGGCCGGGCATGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGC AAAGTGGGACTAGGCCGGGCATGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGC T C ACOT9 Ensembl:ENSG00000123130 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941280994 Functional Loss SNV dbSNP153 33..33 33 - - - 40705 RMVar_ID_40705 Human_SNP_ID_711899477 A-to-I Human chrX - 23772925 23772925 23772925 GAAGGCTGAAGACATGAGAATCGCTTGAACCCAGGGGGCGGAGGTTGCTGAGCTGAGATCATGCC GAAGGCTGAAGACATGAGAATCGCTTGAACCCCGGGGGCGGAGGTTGCTGAGCTGAGATCATGCC T G RF00017-4503,RF00017-049,RF00017-4596 RNACentral:URS00009569F7,RNACentral:URS000096B6E3,RNACentral:URS00009759B0 SRP RNA,SRP RNA,SRP RNA intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1026138510 Functional Loss SNV dbSNP153 33..33 33 - - - 40706 RMVar_ID_40706 Human_SNP_ID_711900915 A-to-I Human chrX - 23779475 23779475 23779475 GGGACTCTCCCACCTCAGCCTCCCAAGTAGCTAGGATTATAGGTGTGTGCCACAATACCTGGCTA GGGACTCTCCCACCTCAGCCTCCCAAGTAGCTTGGATTATAGGTGTGTGCCACAATACCTGGCTA T A AC131011.2 Ensembl:ENSG00000233785 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1454994900 Functional Loss SNV dbSNP153 33..33 33 - - - 40707 RMVar_ID_40707 Human_SNP_ID_711917596 A-to-I Human chrX - 23862651 23862651 23862651 CTCCCATCTCAGCCTCCTGAGTAGCTGCGACTATAGGCATGCACCACCACACCTGACTAATTTTT CTCCCATCTCAGCCTCCTGAGTAGCTGCGACTGTAGGCATGCACCACCACACCTGACTAATTTTT T C APOO Ensembl:ENSG00000184831 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs774539643 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90695,RMVar_hsa_circ_28698,RMVar_hsa_circ_312186,RMVar_hsa_circ_330361,RMVar_hsa_circ_288112,RMVar_hsa_circ_334073,RMVar_hsa_circ_338326,RMVar_hsa_circ_316524,RMVar_hsa_circ_261785,RMVar_hsa_circ_261786 40708 RMVar_ID_40708 Human_SNP_ID_711917607 A-to-I Human chrX - 23862687 23862687 23862687 TCACTGCAGTCTTGACCTCCTCAGGCTCAAGCAATCCTCCCATCTCAGCCTCCTGAGTAGCTGCG TCACTGCAGTCTTGACCTCCTCAGGCTCAAGCGATCCTCCCATCTCAGCCTCCTGAGTAGCTGCG T C APOO Ensembl:ENSG00000184831 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1431830495 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90695,RMVar_hsa_circ_28698,RMVar_hsa_circ_312186,RMVar_hsa_circ_330361,RMVar_hsa_circ_288112,RMVar_hsa_circ_334073,RMVar_hsa_circ_338326,RMVar_hsa_circ_316524,RMVar_hsa_circ_261785,RMVar_hsa_circ_261786 40709 RMVar_ID_40709 Human_SNP_ID_711919783 A-to-I Human chrX - 23873512 23873512 23873512 ACCTTTGTCTCTCAGGTTCAAGCGATTCTCCCACCTTAGCTTCCCGAGTAGCTAGGATTACAAGC ACCTTTGTCTCTCAGGTTCAAGCGATTCTCCCGCCTTAGCTTCCCGAGTAGCTAGGATTACAAGC T C APOO Ensembl:ENSG00000184831 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1477864013 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90695,RMVar_hsa_circ_28698,RMVar_hsa_circ_330361,RMVar_hsa_circ_334073,RMVar_hsa_circ_338326,RMVar_hsa_circ_316524,RMVar_hsa_circ_325029,RMVar_hsa_circ_261786,RMVar_hsa_circ_339474,RMVar_hsa_circ_284788 40710 RMVar_ID_40710 Human_SNP_ID_711947154 A-to-I Human chrX - 24016334 24016334 24016334 TTTTTTTTTTTTTTTTTTTTTTTTTTTGAGACAGAGTCTTGCTCTGTCGCCCAGGCTGGAGTGCA TTTTTTTTTTTTTTTTTTTTTTTTTTTGAGACGGAGTCTTGCTCTGTCGCCCAGGCTGGAGTGCA T C KLHL15 Ensembl:ENSG00000174010 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1470723384 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_315959 40711 RMVar_ID_40711 Human_SNP_ID_711947766 A-to-I Human chrX - 24018751 24018751 24018751 GTGATCAGCCCACCTCTACCTCCCAAGGTGCTAGGATCACGGATGTGAGCCACTGTGCCCGGCTG GTGATCAGCCCACCTCTACCTCCCAAGGTGCTGGGATCACGGATGTGAGCCACTGTGCCCGGCTG T C KLHL15 Ensembl:ENSG00000174010 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs748726829 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26304589 RMVar_hsa_circ_315959 40712 RMVar_ID_40712 Human_SNP_ID_711948471 A-to-I Human chrX - 24022147 24022147 24022147 TATTTTTAGTAGACACGGGGTTTCACCATGTTAGCCAGGCTGGTCTCGACTGACTTCAAGTGATC TATTTTTAGTAGACACGGGGTTTCACCATGTTGGCCAGGCTGGTCTCGACTGACTTCAAGTGATC T C KLHL15 Ensembl:ENSG00000174010 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1372697023 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_315959 40713 RMVar_ID_40713 Human_SNP_ID_711956578 A-to-I Human chrX + 24055857 24055857 24055857 GGTGCAGGGGGAGCACAAAGAATGCTGCCCACATGTAGCTTACAGACTCGGTAAGAAGAAAAAAT GGTGCAGGGGGAGCACAAAGAATGCTGCCCACGTGTAGCTTACAGACTCGGTAAGAAGAAAAAAT A G EIF2S3 Ensembl:ENSG00000130741 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10283978 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_4758,GWAS_ID_4759,GWAS_ID_4760,GWAS_ID_4761,GWAS_ID_4762,GWAS_ID_4763,GWAS_ID_4764,GWAS_ID_4765,GWAS_ID_4766,GWAS_ID_4767,GWAS_ID_4768,GWAS_ID_4769,GWAS_ID_4770,GWAS_ID_4771 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 40714 RMVar_ID_40714 Human_SNP_ID_711956579 A-to-I Human chrX + 24055857 24055857 24055857 GGTGCAGGGGGAGCACAAAGAATGCTGCCCACATGTAGCTTACAGACTCGGTAAGAAGAAAAAAT GGTGCAGGGGGAGCACAAAGAATGCTGCCCACTTGTAGCTTACAGACTCGGTAAGAAGAAAAAAT A T EIF2S3 Ensembl:ENSG00000130741 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10283978 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_4758,GWAS_ID_4759,GWAS_ID_4760,GWAS_ID_4761,GWAS_ID_4762,GWAS_ID_4763,GWAS_ID_4764,GWAS_ID_4765,GWAS_ID_4766,GWAS_ID_4767,GWAS_ID_4768,GWAS_ID_4769,GWAS_ID_4770,GWAS_ID_4771 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 40715 RMVar_ID_40715 Human_SNP_ID_711956742 A-to-I Human chrX + 24056738 24056738 24056738 AAAATTAGCTGTGCGTGGTGGTGCATGCCTGCAGTCCCAGCTACTAAGGAGGCCGAGGTCGGAGG AAAATTAGCTGTGCGTGGTGGTGCATGCCTGCGGTCCCAGCTACTAAGGAGGCCGAGGTCGGAGG A G EIF2S3 Ensembl:ENSG00000130741 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1569277443 Functional Loss SNV dbSNP153 33..33 33 - - - 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 40716 RMVar_ID_40716 Human_SNP_ID_711956743 A-to-I Human chrX + 24056748 24056748 24056748 GTGCGTGGTGGTGCATGCCTGCAGTCCCAGCTACTAAGGAGGCCGAGGTCGGAGGATTGCTCAAG GTGCGTGGTGGTGCATGCCTGCAGTCCCAGCTGCTAAGGAGGCCGAGGTCGGAGGATTGCTCAAG A G EIF2S3 Ensembl:ENSG00000130741 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1276014574 Functional Loss SNV dbSNP153 33..33 33 - - - 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 40717 RMVar_ID_40717 Human_SNP_ID_711960700 A-to-I Human chrX + 24075798 24075798 24075798 TCTCTCTGTTGACCAGGCTGGAGTTTAGTGGCATGATCATAGCTCACTGCAGCCTCAGTGTCTAA TCTCTCTGTTGACCAGGCTGGAGTTTAGTGGCGTGATCATAGCTCACTGCAGCCTCAGTGTCTAA A G EIF2S3 Ensembl:ENSG00000130741 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1235983792 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_257382,Human_RBP_ID_10459005,Human_RBP_ID_16865964,Human_RBP_ID_18918665,Human_RBP_ID_21818663,Human_RBP_ID_23100734,Human_RBP_ID_24338370 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 40718 RMVar_ID_40718 Human_SNP_ID_711960703 A-to-I Human chrX + 24075829 24075821 24075829 CATGATCATAGCTCACTGCAGCCTCAGTGTCTAAGTAGCTAGGACTATTGGCTCACACCACCGTG CATGATCATAGCTCACTGCAGCCTC________AGTAGCTAGGACTATTGGCTCACACCACCGTG CAGTGTCTA C EIF2S3 Ensembl:ENSG00000130741 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1286122674 Functional Loss DEL dbSNP153 26..33 33 - - - Human_RBP_ID_1713959,Human_RBP_ID_10459007,Human_RBP_ID_16865964,Human_RBP_ID_21818668,Human_RBP_ID_23108427 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 40719 RMVar_ID_40719 Human_SNP_ID_711960705 A-to-I Human chrX + 24075833 24075833 24075833 ATCATAGCTCACTGCAGCCTCAGTGTCTAAGTAGCTAGGACTATTGGCTCACACCACCGTGATCA ATCATAGCTCACTGCAGCCTCAGTGTCTAAGTGGCTAGGACTATTGGCTCACACCACCGTGATCA A G EIF2S3 Ensembl:ENSG00000130741 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs759868008 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_733637,Human_RBP_ID_1713959,Human_RBP_ID_7994231,Human_RBP_ID_10459007,Human_RBP_ID_16865964,Human_RBP_ID_21818668,Human_RBP_ID_23108427 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 40720 RMVar_ID_40720 Human_SNP_ID_711960707 A-to-I Human chrX + 24075843 24075843 24075843 ACTGCAGCCTCAGTGTCTAAGTAGCTAGGACTATTGGCTCACACCACCGTGATCAGCTAATTTTT ACTGCAGCCTCAGTGTCTAAGTAGCTAGGACTGTTGGCTCACACCACCGTGATCAGCTAATTTTT A G EIF2S3 Ensembl:ENSG00000130741 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs762765430 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_733637,Human_RBP_ID_7994231,Human_RBP_ID_10459007,Human_RBP_ID_16865964,Human_RBP_ID_21818668,Human_RBP_ID_23108427 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 40721 RMVar_ID_40721 Human_SNP_ID_711960716 A-to-I Human chrX + 24075887 24075887 24075887 CACCGTGATCAGCTAATTTTTTTGTTTTTTGTAGACACTTGGTCTCACTGTGTTGCCCAGCATGA CACCGTGATCAGCTAATTTTTTTGTTTTTTGTGGACACTTGGTCTCACTGTGTTGCCCAGCATGA A G EIF2S3 Ensembl:ENSG00000130741 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs144649547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_733639,Human_RBP_ID_2073199,Human_RBP_ID_3250974,Human_RBP_ID_3920772,Human_RBP_ID_16865964,Human_RBP_ID_23100736 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 40722 RMVar_ID_40722 Human_SNP_ID_711960725 A-to-I Human chrX + 24075951 24075951 24075951 ATCTCAAACTCCTGGCCTCAAGCCATCCTCCCACCTCAGCCTCTCAAAGTGTTGGGATTACAGAC ATCTCAAACTCCTGGCCTCAAGCCATCCTCCCGCCTCAGCCTCTCAAAGTGTTGGGATTACAGAC A G EIF2S3 Ensembl:ENSG00000130741 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs368558977 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8717454,Human_RBP_ID_16865974,Human_RBP_ID_18918666 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 40723 RMVar_ID_40723 Human_SNP_ID_711960727 A-to-I Human chrX + 24075965 24075965 24075965 GCCTCAAGCCATCCTCCCACCTCAGCCTCTCAAAGTGTTGGGATTACAGACATGAGCCACCCCGC GCCTCAAGCCATCCTCCCACCTCAGCCTCTCAGAGTGTTGGGATTACAGACATGAGCCACCCCGC A G EIF2S3 Ensembl:ENSG00000130741 Protein coding intron GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459,32596459 RNA-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 40724 RMVar_ID_40724 Human_SNP_ID_711960730 A-to-I Human chrX + 24075984 24075984 24075984 CCTCAGCCTCTCAAAGTGTTGGGATTACAGACATGAGCCACCCCGCCCAGCCCTGTTTCCTTTAT CCTCAGCCTCTCAAAGTGTTGGGATTACAGACTTGAGCCACCCCGCCCAGCCCTGTTTCCTTTAT A T EIF2S3 Ensembl:ENSG00000130741 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs764753789 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16865975 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 40725 RMVar_ID_40725 Human_SNP_ID_711960973 A-to-I Human chrX + 24077168 24077168 24077168 GGCGTGATCTGCAACCTCTGCCCCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGC GGCGTGATCTGCAACCTCTGCCCCCCGGGTTCGAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGC A G EIF2S3 Ensembl:ENSG00000130741 Protein coding 3'UTR GSE100210;GSE107867 HepG2 cell line;ASD brains,cerebellum - 29129909,30559470 RNA-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 40726 RMVar_ID_40726 Human_SNP_ID_711960980 A-to-I Human chrX + 24077208 24077208 24077208 CTCCTGCCTCAGCCTCCCGAGTAGCTGAGATTACAGGTGCGCGCCACCACACTTGGCTAATTTTT CTCCTGCCTCAGCCTCCCGAGTAGCTGAGATTGCAGGTGCGCGCCACCACACTTGGCTAATTTTT A G EIF2S3 Ensembl:ENSG00000130741 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs3207873 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_733658 Human_miRNA_ID_1401045,Human_miRNA_ID_2231659 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 40727 RMVar_ID_40727 Human_SNP_ID_711960990 A-to-I Human chrX + 24077266 24077266 24077266 AATTTTTGTATTATTAGTAGAGACGGGGTTTCAGCATGTTGGCTAGGCCGGTCTCTCCTGACCTC AATTTTTGTATTATTAGTAGAGACGGGGTTTCGGCATGTTGGCTAGGCCGGTCTCTCCTGACCTC A G EIF2S3 Ensembl:ENSG00000130741 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223225739 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_733660,Human_RBP_ID_2073211,Human_RBP_ID_3251003,Human_RBP_ID_5081458,Human_RBP_ID_7994288,Human_RBP_ID_8226983,Human_RBP_ID_8717465,Human_RBP_ID_16866072,Human_RBP_ID_18149456,Human_RBP_ID_22841229,Human_RBP_ID_23202987,Human_RBP_ID_23216826,Human_RBP_ID_24526533,Human_RBP_ID_26574906,Human_RBP_ID_27147044,Human_RBP_ID_27381276 Human_miRNA_ID_2668563 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 40728 RMVar_ID_40728 Human_SNP_ID_711960995 A-to-I Human chrX + 24077313 24077313 24077313 CCGGTCTCTCCTGACCTCAGGGTGATCAGCCCACCTCGGCCTCACAAAGTGCTGGGATTACAGGC CCGGTCTCTCCTGACCTCAGGGTGATCAGCCCGCCTCGGCCTCACAAAGTGCTGGGATTACAGGC A G EIF2S3 Ensembl:ENSG00000130741 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1368016672 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_733660,Human_RBP_ID_848689,Human_RBP_ID_8226983,Human_RBP_ID_17442676,Human_RBP_ID_18155843 Human_miRNA_ID_1706468,Human_miRNA_ID_2874486,Human_miRNA_ID_2982446 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 40729 RMVar_ID_40729 Human_SNP_ID_711961131 A-to-I Human chrX + 24078079 24078079 24078079 ACGGAGGCTCACTCCGTCACCTAGGCTAGAGTACAGTGGCACGATCTTGGCTCGCTGCAACCTCT ACGGAGGCTCACTCCGTCACCTAGGCTAGAGTGCAGTGGCACGATCTTGGCTCGCTGCAACCTCT A G EIF2S3 Ensembl:ENSG00000130741 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs750699468 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_733687,Human_RBP_ID_16866139,Human_RBP_ID_24338411,Human_RBP_ID_26270885,Human_RBP_ID_26571039 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 40730 RMVar_ID_40730 Human_SNP_ID_711980392 A-to-I Human chrX + 24180527 24180527 24180527 CCTCAGCCTCCCAAGTAGCTGGGATTGTAGGCACGCACCACCACGCCTGGCTAATTTTTTGTATT CCTCAGCCTCCCAAGTAGCTGGGATTGTAGGCCCGCACCACCACGCCTGGCTAATTTTTTGTATT A C ZFX Ensembl:ENSG00000005889 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1345860885 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 40731 RMVar_ID_40731 Human_SNP_ID_711981411 A-to-I Human chrX + 24186516 24186516 24186516 GTGGTGGCATGTGCCTGTGGTTCCAGCTGCTCAGGAGGCAGAGGCAGGAGGATCCCTTGAGCACA GTGGTGGCATGTGCCTGTGGTTCCAGCTGCTCCGGAGGCAGAGGCAGGAGGATCCCTTGAGCACA A C ZFX Ensembl:ENSG00000005889 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1455794859 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16868587 RMVar_hsa_circ_118767,RMVar_hsa_circ_261815,RMVar_hsa_circ_63667,RMVar_hsa_circ_72223,RMVar_hsa_circ_121521,RMVar_hsa_circ_261821 40732 RMVar_ID_40732 Human_SNP_ID_711981697 A-to-I Human chrX + 24188061 24188061 24188061 GGGCATGGTGGTGCGCACCTGTAATCCCAGCTACTCAGGCGGCTGAGTCAGGAGAATCGTTCGAA GGGCATGGTGGTGCGCACCTGTAATCCCAGCTGCTCAGGCGGCTGAGTCAGGAGAATCGTTCGAA A G ZFX Ensembl:ENSG00000005889 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1023308320 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 40733 RMVar_ID_40733 Human_SNP_ID_712106515 A-to-I Human chrX + 24907110 24907110 24907110 CTACTCAGGAGGCTGAGACACGAGAATCATTTAAACCCAGGAGTCGGCGGTTGCAGTGAGCCAAG CTACTCAGGAGGCTGAGACACGAGAATCATTTGAACCCAGGAGTCGGCGGTTGCAGTGAGCCAAG A G POLA1 Ensembl:ENSG00000101868 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417370183 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2759,RMVar_hsa_circ_4891,RMVar_hsa_circ_361897,RMVar_hsa_circ_112233,RMVar_hsa_circ_261852,RMVar_hsa_circ_29624,RMVar_hsa_circ_339299,RMVar_hsa_circ_261862,RMVar_hsa_circ_347537,RMVar_hsa_circ_261876,RMVar_hsa_circ_103764,RMVar_hsa_circ_89090,RMVar_hsa_circ_327363,RMVar_hsa_circ_261868,RMVar_hsa_circ_52529,RMVar_hsa_circ_54739,RMVar_hsa_circ_261869,RMVar_hsa_circ_324470,RMVar_hsa_circ_261874,RMVar_hsa_circ_123263,RMVar_hsa_circ_372851,RMVar_hsa_circ_261877 40734 RMVar_ID_40734 Human_SNP_ID_712535691 A-to-I Human chrX - 27394743 27394743 27394743 ATTTTTGAGACAGGGTCTCACTCTGTCACCCAAGCTGGAATGCAGTGGTGTGATCACGGCTTATG ATTTTTGAGACAGGGTCTCACTCTGTCACCCACGCTGGAATGCAGTGGTGTGATCACGGCTTATG T G AC107419.1 Ensembl:ENSG00000228933 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs534394982 Functional Loss SNV dbSNP153 33..33 33 - - - 40735 RMVar_ID_40735 Human_SNP_ID_712602122 A-to-I Human chrX + 27748037 27748037 27748037 TACAATTACTGTGAATCCCGCCAATACCTACCAATTTGCAGTGGGTGGACAAGATCAGTTTGTAA TACAATTACTGTGAATCCCGCCAATACCTACCGATTTGCAGTGGGTGGACAAGATCAGTTTGTAA A G DCAF8L2 Ensembl:ENSG00000189186 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459789404 Functional Loss SNV dbSNP153 33..33 33 - - - 40736 RMVar_ID_40736 Human_SNP_ID_712818309 A-to-I Human chrX + 29009065 29009065 29009065 CATGTCCTCTGCAGCAACGTAGATGTGGCTGGAAGCCATTAGCCAAAGCAAACTAATGCAGGAAC CATGTCCTCTGCAGCAACGTAGATGTGGCTGGGAGCCATTAGCCAAAGCAAACTAATGCAGGAAC A G IL1RAPL1 Ensembl:ENSG00000169306 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1443077915 Functional Loss SNV dbSNP153 33..33 33 - - - 40737 RMVar_ID_40737 Human_SNP_ID_712818361 A-to-I Human chrX + 29009303 29009303 29009303 AATCATTTGTACACCAAATCCCAGTGGCACACAATTTACTCATGTAACAAACCTGCACATGTACC AATCATTTGTACACCAAATCCCAGTGGCACACTATTTACTCATGTAACAAACCTGCACATGTACC A T IL1RAPL1 Ensembl:ENSG00000169306 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs888247876 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9246471 40738 RMVar_ID_40738 Human_SNP_ID_628964660 A-to-I Human chr17 - 60050935 60050935 60050935 TCTGGACTATGATGCTGAACGGTCCTTTACCCAGAGCCCTGCAGAATTCAGAACACCCAACTCTC TCTGGACTATGATGCTGAACGGTCCTTTACCCGGAGCCCTGCAGAATTCAGAACACCCAACTCTC T C HEATR6 Ensembl:ENSG00000068097 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1318395614 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_896745,Human_RBP_ID_1865055,Human_RBP_ID_3950915,Human_RBP_ID_13108047,Human_RBP_ID_18991916 Human_Splice_Rec_1848368,Human_Splice_Rec_1848369,Human_Splice_Rec_1848401,Human_Splice_Rec_1848431,Human_Splice_Rec_1848466,Human_Splice_Rec_1848467,Human_Splice_Rec_1848484,Human_Splice_Rec_1848485 Human_miRNA_ID_2425417,Human_miRNA_ID_2435081,Human_miRNA_ID_3069955 RMVar_hsa_circ_9078,RMVar_hsa_circ_100966,RMVar_hsa_circ_185892,RMVar_hsa_circ_185893,RMVar_hsa_circ_95514 40739 RMVar_ID_40739 Human_SNP_ID_629005273 A-to-I Human chr17 - 60233400 60233400 60233400 GCTGGAGTGTAGTGGCACAATCATAGCTCACTACAGCCTCAACCTCATGGACTGAGGCAATTCTC GCTGGAGTGTAGTGGCACAATCATAGCTCACTGCAGCCTCAACCTCATGGACTGAGGCAATTCTC T C USP32 Ensembl:ENSG00000170832 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1425519047 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87386,RMVar_hsa_circ_117624,RMVar_hsa_circ_185897,RMVar_hsa_circ_185901,RMVar_hsa_circ_102961,RMVar_hsa_circ_185903,RMVar_hsa_circ_369284,RMVar_hsa_circ_99427,RMVar_hsa_circ_185906,RMVar_hsa_circ_185905,RMVar_hsa_circ_185927,RMVar_hsa_circ_81288,RMVar_hsa_circ_126316,RMVar_hsa_circ_185916,RMVar_hsa_circ_185918,RMVar_hsa_circ_185919,RMVar_hsa_circ_124858,RMVar_hsa_circ_185920,RMVar_hsa_circ_370202,RMVar_hsa_circ_368822,RMVar_hsa_circ_50707,RMVar_hsa_circ_7604,RMVar_hsa_circ_45904,RMVar_hsa_circ_370230,RMVar_hsa_circ_185923,RMVar_hsa_circ_9637,RMVar_hsa_circ_359114,RMVar_hsa_circ_99894,RMVar_hsa_circ_185929,RMVar_hsa_circ_320303,RMVar_hsa_circ_331484,RMVar_hsa_circ_376547,RMVar_hsa_circ_362447,RMVar_hsa_circ_328493 40740 RMVar_ID_40740 Human_SNP_ID_629013020 A-to-I Human chr17 - 60267661 60267661 60267661 CAAAAGTTAGCCGGGCGTGGTGGTGGACACCTATAGTCCCAGCTACTCGGGAGGCTGAGGCAGGA CAAAAGTTAGCCGGGCGTGGTGGTGGACACCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGA T C USP32 Ensembl:ENSG00000170832 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs764687375 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87386,RMVar_hsa_circ_117624,RMVar_hsa_circ_185897,RMVar_hsa_circ_185901,RMVar_hsa_circ_102961,RMVar_hsa_circ_185903,RMVar_hsa_circ_99427,RMVar_hsa_circ_185905,RMVar_hsa_circ_185927,RMVar_hsa_circ_81288,RMVar_hsa_circ_126316,RMVar_hsa_circ_185916,RMVar_hsa_circ_185918,RMVar_hsa_circ_185919,RMVar_hsa_circ_124858,RMVar_hsa_circ_185920,RMVar_hsa_circ_370202,RMVar_hsa_circ_368822,RMVar_hsa_circ_7604,RMVar_hsa_circ_370230,RMVar_hsa_circ_185923,RMVar_hsa_circ_99894,RMVar_hsa_circ_185935,RMVar_hsa_circ_80930,RMVar_hsa_circ_320303,RMVar_hsa_circ_362447,RMVar_hsa_circ_70008,RMVar_hsa_circ_369049,RMVar_hsa_circ_334655,RMVar_hsa_circ_185930,RMVar_hsa_circ_334995,RMVar_hsa_circ_185931,RMVar_hsa_circ_378362,RMVar_hsa_circ_335172,RMVar_hsa_circ_320343,RMVar_hsa_circ_185933,RMVar_hsa_circ_185934,RMVar_hsa_circ_325580,RMVar_hsa_circ_317594,RMVar_hsa_circ_43971,RMVar_hsa_circ_185939,RMVar_hsa_circ_276134,RMVar_hsa_circ_293780,RMVar_hsa_circ_354006,RMVar_hsa_circ_301646,RMVar_hsa_circ_283028,RMVar_hsa_circ_270166,RMVar_hsa_circ_185940,RMVar_hsa_circ_185937,RMVar_hsa_circ_185938,RMVar_hsa_circ_325125,RMVar_hsa_circ_185936,RMVar_hsa_circ_314960,RMVar_hsa_circ_185942,RMVar_hsa_circ_185943 40741 RMVar_ID_40741 Human_SNP_ID_629014691 A-to-I Human chr17 - 60275277 60275275 60275277 AATTTTTGTATTTTTAGTAGAGATGGCGTTTCACCATGTTTCCTAGGCTGGTCTTGTACTCCTGA AATTTTTGTATTTTTAGTAGAGATGGCGTTTC__CATGTTTCCTAGGCTGGTCTTGTACTCCTGA GGT G USP32 Ensembl:ENSG00000170832 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1442621205 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_368822,RMVar_hsa_circ_7604,RMVar_hsa_circ_370230,RMVar_hsa_circ_185923,RMVar_hsa_circ_185935,RMVar_hsa_circ_320303,RMVar_hsa_circ_70008,RMVar_hsa_circ_369049,RMVar_hsa_circ_334995,RMVar_hsa_circ_378362,RMVar_hsa_circ_335172,RMVar_hsa_circ_185933,RMVar_hsa_circ_185934,RMVar_hsa_circ_317594,RMVar_hsa_circ_43971,RMVar_hsa_circ_185939,RMVar_hsa_circ_276134,RMVar_hsa_circ_354006,RMVar_hsa_circ_283028,RMVar_hsa_circ_270166,RMVar_hsa_circ_185937,RMVar_hsa_circ_185938,RMVar_hsa_circ_185936,RMVar_hsa_circ_47938,RMVar_hsa_circ_185943,RMVar_hsa_circ_308901,RMVar_hsa_circ_375549,RMVar_hsa_circ_185945,RMVar_hsa_circ_185946,RMVar_hsa_circ_277403,RMVar_hsa_circ_185948 40742 RMVar_ID_40742 Human_SNP_ID_629015314 A-to-I Human chr17 - 60278190 60278190 60278190 TTTAAAATTTTTATTTATTGTCTGGGTGCAGTAGCTCATGCCTGTAATCCCAGCACTTTGGAAGG TTTAAAATTTTTATTTATTGTCTGGGTGCAGTGGCTCATGCCTGTAATCCCAGCACTTTGGAAGG T C USP32 Ensembl:ENSG00000170832 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886169301 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_368822,RMVar_hsa_circ_7604,RMVar_hsa_circ_370230,RMVar_hsa_circ_185923,RMVar_hsa_circ_185935,RMVar_hsa_circ_320303,RMVar_hsa_circ_70008,RMVar_hsa_circ_369049,RMVar_hsa_circ_334995,RMVar_hsa_circ_378362,RMVar_hsa_circ_335172,RMVar_hsa_circ_185933,RMVar_hsa_circ_185934,RMVar_hsa_circ_317594,RMVar_hsa_circ_43971,RMVar_hsa_circ_185939,RMVar_hsa_circ_276134,RMVar_hsa_circ_354006,RMVar_hsa_circ_283028,RMVar_hsa_circ_270166,RMVar_hsa_circ_185937,RMVar_hsa_circ_185938,RMVar_hsa_circ_185936,RMVar_hsa_circ_47938,RMVar_hsa_circ_185943,RMVar_hsa_circ_308901,RMVar_hsa_circ_375549,RMVar_hsa_circ_185945,RMVar_hsa_circ_185946,RMVar_hsa_circ_277403,RMVar_hsa_circ_185948 40743 RMVar_ID_40743 Human_SNP_ID_629019635 A-to-I Human chr17 - 60297614 60297614 60297614 TAATATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCTGGGCGTGTGACTGTAATCCC TAATATGGTGAAACCCCGTCTCTACTAAAAATTCAAAAATTAGCTGGGCGTGTGACTGTAATCCC T A USP32 Ensembl:ENSG00000170832 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1189085286 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_370230,RMVar_hsa_circ_185923,RMVar_hsa_circ_369049,RMVar_hsa_circ_378362,RMVar_hsa_circ_43971,RMVar_hsa_circ_354006,RMVar_hsa_circ_270166,RMVar_hsa_circ_185937,RMVar_hsa_circ_185936,RMVar_hsa_circ_47938,RMVar_hsa_circ_185943,RMVar_hsa_circ_375549,RMVar_hsa_circ_185946,RMVar_hsa_circ_185950,RMVar_hsa_circ_309649,RMVar_hsa_circ_306924,RMVar_hsa_circ_185951,RMVar_hsa_circ_310378,RMVar_hsa_circ_312837 40744 RMVar_ID_40744 Human_SNP_ID_629023858 A-to-I Human chr17 - 60316675 60316675 60316675 CACCACACCCGACTCATTTTTGTATTTTTAGTAGAGACGGGATTTCACCATGTTGGCCAGTCTGG CACCACACCCGACTCATTTTTGTATTTTTAGTGGAGACGGGATTTCACCATGTTGGCCAGTCTGG T C USP32 Ensembl:ENSG00000170832 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1429347222 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_370230,RMVar_hsa_circ_185923,RMVar_hsa_circ_369049,RMVar_hsa_circ_378362,RMVar_hsa_circ_43971,RMVar_hsa_circ_270166,RMVar_hsa_circ_185936,RMVar_hsa_circ_185943,RMVar_hsa_circ_375549,RMVar_hsa_circ_185946,RMVar_hsa_circ_306924,RMVar_hsa_circ_185951,RMVar_hsa_circ_312837 40745 RMVar_ID_40745 Human_SNP_ID_629025872 A-to-I Human chr17 - 60326475 60326475 60326475 GGCCAACAGTCCCTACCAAAAATACAAAAATTAGCCGAGCATGGTTGTCGGTGCCTGTAATCCCA GGCCAACAGTCCCTACCAAAAATACAAAAATTGGCCGAGCATGGTTGTCGGTGCCTGTAATCCCA T C USP32 Ensembl:ENSG00000170832 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs745832586 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_370230,RMVar_hsa_circ_185923,RMVar_hsa_circ_369049,RMVar_hsa_circ_378362,RMVar_hsa_circ_43971,RMVar_hsa_circ_270166,RMVar_hsa_circ_185936,RMVar_hsa_circ_185943,RMVar_hsa_circ_375549,RMVar_hsa_circ_185946,RMVar_hsa_circ_306924,RMVar_hsa_circ_185951,RMVar_hsa_circ_312837 40746 RMVar_ID_40746 Human_SNP_ID_629026871 A-to-I Human chr17 - 60330625 60330625 60330625 GGAGGATTGATTAAGCCTGGGAGGTTGAGGCTACAGTGAACCATGATTGCACCACTGCACTCCGA GGAGGATTGATTAAGCCTGGGAGGTTGAGGCTTCAGTGAACCATGATTGCACCACTGCACTCCGA T A USP32 Ensembl:ENSG00000170832 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1020401804 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_370230,RMVar_hsa_circ_185923,RMVar_hsa_circ_369049,RMVar_hsa_circ_378362,RMVar_hsa_circ_43971,RMVar_hsa_circ_270166,RMVar_hsa_circ_185936,RMVar_hsa_circ_185943,RMVar_hsa_circ_375549,RMVar_hsa_circ_185946,RMVar_hsa_circ_306924,RMVar_hsa_circ_185951,RMVar_hsa_circ_312837 40747 RMVar_ID_40747 Human_SNP_ID_629057502 A-to-I Human chr17 - 60458251 60458251 60458251 TTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGACTGGTCTCGATCTCCTGACCT TTTTGTATTTTTAGTAGAGACAGGGTTTCACCGTGTTGGCCAGACTGGTCTCGATCTCCTGACCT T C APPBP2 Ensembl:ENSG00000062725 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs758999455 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_30463,RMVar_hsa_circ_46439,RMVar_hsa_circ_269949,RMVar_hsa_circ_269309,RMVar_hsa_circ_286003,RMVar_hsa_circ_269442,RMVar_hsa_circ_185954,RMVar_hsa_circ_42973,RMVar_hsa_circ_288614,RMVar_hsa_circ_185953,RMVar_hsa_circ_321070,RMVar_hsa_circ_185958,RMVar_hsa_circ_314181,RMVar_hsa_circ_185957,RMVar_hsa_circ_9182,RMVar_hsa_circ_357082,RMVar_hsa_circ_85018,RMVar_hsa_circ_294200,RMVar_hsa_circ_185959,RMVar_hsa_circ_185960 40748 RMVar_ID_40748 Human_SNP_ID_629057510 A-to-I Human chr17 - 60458286 60458286 60458286 GGAATTACAGGCACACGCCACCACACCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCA GGAATTACAGGCACACGCCACCACACCTGGCTGATTTTTGTATTTTTAGTAGAGACAGGGTTTCA T C APPBP2 Ensembl:ENSG00000062725 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs947532761 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_30463,RMVar_hsa_circ_46439,RMVar_hsa_circ_269949,RMVar_hsa_circ_269309,RMVar_hsa_circ_286003,RMVar_hsa_circ_269442,RMVar_hsa_circ_185954,RMVar_hsa_circ_42973,RMVar_hsa_circ_288614,RMVar_hsa_circ_185953,RMVar_hsa_circ_321070,RMVar_hsa_circ_185958,RMVar_hsa_circ_314181,RMVar_hsa_circ_185957,RMVar_hsa_circ_9182,RMVar_hsa_circ_357082,RMVar_hsa_circ_85018,RMVar_hsa_circ_294200,RMVar_hsa_circ_185959,RMVar_hsa_circ_185960 40749 RMVar_ID_40749 Human_SNP_ID_629057939 A-to-I Human chr17 - 60459630 60459630 60459630 AAAATTAGCCGGGCATGGTGGTGGGCACTTGTAATCCCAGCTATTCGGGAGGCTGAGGCAGACAA AAAATTAGCCGGGCATGGTGGTGGGCACTTGTTATCCCAGCTATTCGGGAGGCTGAGGCAGACAA T A APPBP2 Ensembl:ENSG00000062725 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1371462605 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_30463,RMVar_hsa_circ_46439,RMVar_hsa_circ_269949,RMVar_hsa_circ_269309,RMVar_hsa_circ_286003,RMVar_hsa_circ_269442,RMVar_hsa_circ_185954,RMVar_hsa_circ_42973,RMVar_hsa_circ_288614,RMVar_hsa_circ_185953,RMVar_hsa_circ_321070,RMVar_hsa_circ_185958,RMVar_hsa_circ_314181,RMVar_hsa_circ_185957,RMVar_hsa_circ_9182,RMVar_hsa_circ_357082,RMVar_hsa_circ_85018,RMVar_hsa_circ_294200,RMVar_hsa_circ_185959,RMVar_hsa_circ_185960 40750 RMVar_ID_40750 Human_SNP_ID_629068533 A-to-I Human chr17 - 60501211 60501211 60501211 AACTCCTGGGCTCAAGCAGTCCCCTTGCCTCAACCTCCCAAATAGCTGAGACTACAGGTGCATGC AACTCCTGGGCTCAAGCAGTCCCCTTGCCTCAGCCTCCCAAATAGCTGAGACTACAGGTGCATGC T C APPBP2 Ensembl:ENSG00000062725 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270696525 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_185971,RMVar_hsa_circ_185970 40751 RMVar_ID_40751 Human_SNP_ID_629068886 A-to-I Human chr17 - 60502700 60502700 60502700 AGGTGCCTGCCACCATGGCCTGTTTAATTTTTATATTTTTAGTAGAGACAGGATTTCTCCATGTT AGGTGCCTGCCACCATGGCCTGTTTAATTTTTGTATTTTTAGTAGAGACAGGATTTCTCCATGTT T C APPBP2 Ensembl:ENSG00000062725 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs907845003 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_185971,RMVar_hsa_circ_185970 40752 RMVar_ID_40752 Human_SNP_ID_629068893 A-to-I Human chr17 - 60502744 60502744 60502744 AGTTCAAGCGATTCTCTCCCAGCCTCCCGAGTAGCTGGGATTACAGGTGCCTGCCACCATGGCCT AGTTCAAGCGATTCTCTCCCAGCCTCCCGAGTGGCTGGGATTACAGGTGCCTGCCACCATGGCCT T C APPBP2 Ensembl:ENSG00000062725 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs368269263 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_185971,RMVar_hsa_circ_185970 40753 RMVar_ID_40753 Human_SNP_ID_629071845 A-to-I Human chr17 + 60513316 60513316 60513316 TCAATGTATATTTGGGAAATATGGACCTATTCATCAAATCAGAGTGGAAAACACACCTGAAACTA TCAATGTATATTTGGGAAATATGGACCTATTCGTCAAATCAGAGTGGAAAACACACCTGAAACTA A G AC011921.3 Ensembl:ENSG00000270553 Pseudogene exon GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs879039940 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5579877,Human_RBP_ID_9078115 40754 RMVar_ID_40754 Human_SNP_ID_629071851 A-to-I Human chr17 + 60513331 60513331 60513331 GAAATATGGACCTATTCATCAAATCAGAGTGGAAAACACACCTGAAACTAGAGGAACAGCTTATG GAAATATGGACCTATTCATCAAATCAGAGTGGGAAACACACCTGAAACTAGAGGAACAGCTTATG A G AC011921.3 Ensembl:ENSG00000270553 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879125901 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5579877 40755 RMVar_ID_40755 Human_SNP_ID_629072137 A-to-I Human chr17 - 60514349 60514349 60514349 TTCCTGCCTTGGCTTCCTAAAGTGCTGGTATTATAGGTATGAGCCACCTTGCCTAGCCTCCATTG TTCCTGCCTTGGCTTCCTAAAGTGCTGGTATTGTAGGTATGAGCCACCTTGCCTAGCCTCCATTG T C APPBP2 Ensembl:ENSG00000062725 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1472704874 Functional Loss SNV dbSNP153 33..33 33 - - - 40756 RMVar_ID_40756 Human_SNP_ID_629073137 A-to-I Human chr17 - 60518201 60518201 60518201 CTCAACCAAAAACAATAAAAAATAAGCTAGGCATGGCGACATACACCTGTAGTGCCAGTTACTTG CTCAACCAAAAACAATAAAAAATAAGCTAGGCTTGGCGACATACACCTGTAGTGCCAGTTACTTG T A APPBP2 Ensembl:ENSG00000062725 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1302371399 Functional Loss SNV dbSNP153 33..33 33 - - - 40757 RMVar_ID_40757 Human_SNP_ID_629073631 A-to-I Human chr17 - 60519547 60519547 60519547 GTGATCCTCCTGCCTCATCGTCCCGAGTAGCTAGGACTACAGATGCTTGCCACCACACCTGGTTA GTGATCCTCCTGCCTCATCGTCCCGAGTAGCTGGGACTACAGATGCTTGCCACCACACCTGGTTA T C APPBP2 Ensembl:ENSG00000062725 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1390706515 Functional Loss SNV dbSNP153 33..33 33 - - - 40758 RMVar_ID_40758 Human_SNP_ID_629077508 A-to-I Human chr17 + 60534482 60534482 60534482 TTGTGTAGGCTGTAGTCCAGTGGTACAATCATAGCTCACTGCAGCTTCTAACTGCCGGGCTCAAG TTGTGTAGGCTGTAGTCCAGTGGTACAATCATGGCTCACTGCAGCTTCTAACTGCCGGGCTCAAG A G AC011921.1 Ensembl:ENSG00000259349 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs963984253 Functional Loss SNV dbSNP153 33..33 33 - - - 40759 RMVar_ID_40759 Human_SNP_ID_629102533 A-to-I Human chr17 + 60635398 60635398 60635398 CCACCACTACCGGCTAATTTTGTATTTTTAGTAGAGACGGGGTTTCTCTATGTTGGTCAGACTGG CCACCACTACCGGCTAATTTTGTATTTTTAGTGGAGACGGGGTTTCTCTATGTTGGTCAGACTGG A G PPM1D Ensembl:ENSG00000170836 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs575479894 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6251,RMVar_hsa_circ_292953,RMVar_hsa_circ_320273,RMVar_hsa_circ_289849,RMVar_hsa_circ_185973,RMVar_hsa_circ_185974,RMVar_hsa_circ_359161,RMVar_hsa_circ_185977,RMVar_hsa_circ_283700,RMVar_hsa_circ_185976 40760 RMVar_ID_40760 Human_SNP_ID_629116040 A-to-I Human chr17 + 60687483 60687483 60687483 AAAATTAGCTGGGTGTGGTGGTGCACACCTGTAGTCCCAGCTATTTGGGAGGCTGACATGGGTGG AAAATTAGCTGGGTGTGGTGGTGCACACCTGTGGTCCCAGCTATTTGGGAGGCTGACATGGGTGG A G BCAS3 Ensembl:ENSG00000141376 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1311362315 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7646,RMVar_hsa_circ_43085,RMVar_hsa_circ_304309,RMVar_hsa_circ_185980,RMVar_hsa_circ_315109,RMVar_hsa_circ_357298,RMVar_hsa_circ_367234,RMVar_hsa_circ_366078,RMVar_hsa_circ_317392,RMVar_hsa_circ_314049,RMVar_hsa_circ_315009,RMVar_hsa_circ_307989,RMVar_hsa_circ_293172,RMVar_hsa_circ_296238,RMVar_hsa_circ_297886,RMVar_hsa_circ_294106,RMVar_hsa_circ_68782,RMVar_hsa_circ_285782,RMVar_hsa_circ_44438,RMVar_hsa_circ_120047,RMVar_hsa_circ_185984,RMVar_hsa_circ_185986,RMVar_hsa_circ_185988,RMVar_hsa_circ_185987,RMVar_hsa_circ_185985,RMVar_hsa_circ_185982,RMVar_hsa_circ_185983,RMVar_hsa_circ_331243,RMVar_hsa_circ_185981,RMVar_hsa_circ_320903,RMVar_hsa_circ_77788,RMVar_hsa_circ_106810,RMVar_hsa_circ_31175,RMVar_hsa_circ_185991,RMVar_hsa_circ_185993,RMVar_hsa_circ_185994,RMVar_hsa_circ_185992,RMVar_hsa_circ_185990 40761 RMVar_ID_40761 Human_SNP_ID_629203316 A-to-I Human chr17 + 61059905 61059905 61059905 AAAATTAGCCGGGCGTGGTGGCGCGTGCCTGTAATCCCAGCCACTCGGGAAGGCTGAGGCAGGAC AAAATTAGCCGGGCGTGGTGGCGCGTGCCTGTGATCCCAGCCACTCGGGAAGGCTGAGGCAGGAC A G BCAS3 Ensembl:ENSG00000141376 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1448014027 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43085,RMVar_hsa_circ_307989,RMVar_hsa_circ_294106,RMVar_hsa_circ_68782,RMVar_hsa_circ_185981,RMVar_hsa_circ_106810,RMVar_hsa_circ_68336,RMVar_hsa_circ_185994,RMVar_hsa_circ_74096,RMVar_hsa_circ_115241,RMVar_hsa_circ_186000,RMVar_hsa_circ_372524,RMVar_hsa_circ_186003,RMVar_hsa_circ_351723,RMVar_hsa_circ_85875,RMVar_hsa_circ_186006,RMVar_hsa_circ_186007,RMVar_hsa_circ_34015,RMVar_hsa_circ_30627,RMVar_hsa_circ_374257,RMVar_hsa_circ_66836,RMVar_hsa_circ_186015,RMVar_hsa_circ_186016,RMVar_hsa_circ_47929,RMVar_hsa_circ_331436,RMVar_hsa_circ_186018,RMVar_hsa_circ_313201,RMVar_hsa_circ_80074,RMVar_hsa_circ_73950,RMVar_hsa_circ_186020,RMVar_hsa_circ_308776,RMVar_hsa_circ_32343,RMVar_hsa_circ_370351,RMVar_hsa_circ_186022,RMVar_hsa_circ_186023,RMVar_hsa_circ_186024 40762 RMVar_ID_40762 Human_SNP_ID_629211617 A-to-I Human chr17 + 61095596 61095596 61095596 TCAAGTGCTTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTCCAGGCATGCACCACCATGCCCG TCAAGTGCTTCTCCTGCCTCAGCCTCCCGAGTTGCTGGGACTCCAGGCATGCACCACCATGCCCG A T BCAS3 Ensembl:ENSG00000141376 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903655936 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_307989,RMVar_hsa_circ_115241,RMVar_hsa_circ_186000,RMVar_hsa_circ_85875,RMVar_hsa_circ_186007,RMVar_hsa_circ_66836,RMVar_hsa_circ_80074,RMVar_hsa_circ_186023 40763 RMVar_ID_40763 Human_SNP_ID_629223201 A-to-I Human chr17 + 61146951 61146946 61146951 AAAAAAATTTTTTTAAGACAGGGTCTTGCTCTATTGCCCAGGCTGGAGTGCAGTGGCGTGATCAT AAAAAAATTTTTTTAAGACAGGGTCTTG_____TTGCCCAGGCTGGAGTGCAGTGGCGTGATCAT GCTCTA G BCAS3 Ensembl:ENSG00000141376 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1219159710 Functional Loss DEL dbSNP153 29..33 33 - - - RMVar_hsa_circ_307989,RMVar_hsa_circ_115241,RMVar_hsa_circ_186000,RMVar_hsa_circ_85875,RMVar_hsa_circ_186007,RMVar_hsa_circ_66836,RMVar_hsa_circ_80074,RMVar_hsa_circ_186023 40764 RMVar_ID_40764 Human_SNP_ID_629223202 A-to-I Human chr17 + 61146951 61146951 61146951 AAAAAAATTTTTTTAAGACAGGGTCTTGCTCTATTGCCCAGGCTGGAGTGCAGTGGCGTGATCAT AAAAAAATTTTTTTAAGACAGGGTCTTGCTCTGTTGCCCAGGCTGGAGTGCAGTGGCGTGATCAT A G BCAS3 Ensembl:ENSG00000141376 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1021730012 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_307989,RMVar_hsa_circ_115241,RMVar_hsa_circ_186000,RMVar_hsa_circ_85875,RMVar_hsa_circ_186007,RMVar_hsa_circ_66836,RMVar_hsa_circ_80074,RMVar_hsa_circ_186023 40765 RMVar_ID_40765 Human_SNP_ID_629228726 A-to-I Human chr17 + 61171695 61171695 61171695 AAGGCTGATATGCAGTGACATGATTACAGCTCACTGCAGCCTCAAACTCCTGGGCTCAAGTCATC AAGGCTGATATGCAGTGACATGATTACAGCTCCCTGCAGCCTCAAACTCCTGGGCTCAAGTCATC A C BCAS3 Ensembl:ENSG00000141376 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs922069637 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_307989,RMVar_hsa_circ_115241,RMVar_hsa_circ_186000,RMVar_hsa_circ_85875,RMVar_hsa_circ_186007,RMVar_hsa_circ_66836,RMVar_hsa_circ_80074,RMVar_hsa_circ_186023 40766 RMVar_ID_40766 Human_SNP_ID_629228738 A-to-I Human chr17 + 61171762 61171762 61171762 CCTGCTTCAGCCTCCTGAGTAGCTGGGATTTCAGGCATGTGCCACCATGCCCTGCTAATTAAAAA CCTGCTTCAGCCTCCTGAGTAGCTGGGATTTCCGGCATGTGCCACCATGCCCTGCTAATTAAAAA A C BCAS3 Ensembl:ENSG00000141376 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1568500597 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_307989,RMVar_hsa_circ_115241,RMVar_hsa_circ_186000,RMVar_hsa_circ_85875,RMVar_hsa_circ_186007,RMVar_hsa_circ_66836,RMVar_hsa_circ_80074,RMVar_hsa_circ_186023 40767 RMVar_ID_40767 Human_SNP_ID_629229636 A-to-I Human chr17 + 61175300 61175300 61175300 GTGGTGGTGCATGGCCATAGTCCCAGCTACTCAGGAGACTGAGGCAGGAGGATCACTTGAGTTTG GTGGTGGTGCATGGCCATAGTCCCAGCTACTCGGGAGACTGAGGCAGGAGGATCACTTGAGTTTG A G BCAS3 Ensembl:ENSG00000141376 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1472818494 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_307989,RMVar_hsa_circ_115241,RMVar_hsa_circ_186000,RMVar_hsa_circ_85875,RMVar_hsa_circ_186007,RMVar_hsa_circ_66836,RMVar_hsa_circ_80074,RMVar_hsa_circ_186023 40768 RMVar_ID_40768 Human_SNP_ID_629230025 A-to-I Human chr17 + 61176835 61176835 61176835 CTCCTGCCTCAGCCTCCCAAAGTGCCAGGATTATAGGCATGAGCCACCGCACTCTGGCCTCAATC CTCCTGCCTCAGCCTCCCAAAGTGCCAGGATTGTAGGCATGAGCCACCGCACTCTGGCCTCAATC A G BCAS3 Ensembl:ENSG00000141376 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1186550769 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_307989,RMVar_hsa_circ_115241,RMVar_hsa_circ_186000,RMVar_hsa_circ_85875,RMVar_hsa_circ_186007,RMVar_hsa_circ_66836,RMVar_hsa_circ_80074,RMVar_hsa_circ_186023 40769 RMVar_ID_40769 Human_SNP_ID_629256951 A-to-I Human chr17 + 61295749 61295749 61295749 CCGAGGCGGGTGGATCACGAGGTCAGGAGTTCAAGACCAGCCTGACCAACATGGTGAAACCCCCG CCGAGGCGGGTGGATCACGAGGTCAGGAGTTCGAGACCAGCCTGACCAACATGGTGAAACCCCCG A G BCAS3 Ensembl:ENSG00000141376 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1135702 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_307989,RMVar_hsa_circ_115241,RMVar_hsa_circ_186000,RMVar_hsa_circ_85875,RMVar_hsa_circ_186007,RMVar_hsa_circ_66836,RMVar_hsa_circ_80074,RMVar_hsa_circ_186023 40770 RMVar_ID_40770 Human_SNP_ID_629358836 A-to-I Human chr17 - 61719967 61719967 61719967 AAAATTGGCCAGGCATGGCAGCACACACCTGTAGTCCAACCTACTTGGGAGGCTGAGGTGGGAGA AAAATTGGCCAGGCATGGCAGCACACACCTGTGGTCCAACCTACTTGGGAGGCTGAGGTGGGAGA T C BRIP1 Ensembl:ENSG00000136492 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1183435578 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_186032,RMVar_hsa_circ_296404,RMVar_hsa_circ_331137,RMVar_hsa_circ_356373,RMVar_hsa_circ_186030,RMVar_hsa_circ_372755,RMVar_hsa_circ_336547,RMVar_hsa_circ_314360,RMVar_hsa_circ_96568,RMVar_hsa_circ_96907,RMVar_hsa_circ_42812,RMVar_hsa_circ_70611,RMVar_hsa_circ_329914,RMVar_hsa_circ_340649,RMVar_hsa_circ_353125,RMVar_hsa_circ_363391,RMVar_hsa_circ_186031,RMVar_hsa_circ_360154,RMVar_hsa_circ_347633,RMVar_hsa_circ_338801,RMVar_hsa_circ_315987,RMVar_hsa_circ_321145,RMVar_hsa_circ_309924 40771 RMVar_ID_40771 Human_SNP_ID_629374417 A-to-I Human chr17 - 61791406 61791406 61791406 CGGCTCACTGCAACCTCTGCCTCTCGTGTTCAAGTGATCCTCATGTCTAAGCCTCCTGAGTTGCT CGGCTCACTGCAACCTCTGCCTCTCGTGTTCAGGTGATCCTCATGTCTAAGCCTCCTGAGTTGCT T C BRIP1 Ensembl:ENSG00000136492 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1366576932 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13116449 RMVar_hsa_circ_40097,RMVar_hsa_circ_186032,RMVar_hsa_circ_296404,RMVar_hsa_circ_331137,RMVar_hsa_circ_96568,RMVar_hsa_circ_42812,RMVar_hsa_circ_70611,RMVar_hsa_circ_340649,RMVar_hsa_circ_360154,RMVar_hsa_circ_338801,RMVar_hsa_circ_321145,RMVar_hsa_circ_347800,RMVar_hsa_circ_363818,RMVar_hsa_circ_346003,RMVar_hsa_circ_333198,RMVar_hsa_circ_92865,RMVar_hsa_circ_18542,RMVar_hsa_circ_186039,RMVar_hsa_circ_275989,RMVar_hsa_circ_65119,RMVar_hsa_circ_186033,RMVar_hsa_circ_186034,RMVar_hsa_circ_69229,RMVar_hsa_circ_295911,RMVar_hsa_circ_320794,RMVar_hsa_circ_308778,RMVar_hsa_circ_287108,RMVar_hsa_circ_288036,RMVar_hsa_circ_63938,RMVar_hsa_circ_275035,RMVar_hsa_circ_81566,RMVar_hsa_circ_186043,RMVar_hsa_circ_186041,RMVar_hsa_circ_186042,RMVar_hsa_circ_186040,RMVar_hsa_circ_9922,RMVar_hsa_circ_186038,RMVar_hsa_circ_264785,RMVar_hsa_circ_112995,RMVar_hsa_circ_47028,RMVar_hsa_circ_186049,RMVar_hsa_circ_299195,RMVar_hsa_circ_359136,RMVar_hsa_circ_84616,RMVar_hsa_circ_186050,RMVar_hsa_circ_186051,RMVar_hsa_circ_59655 40772 RMVar_ID_40772 Human_SNP_ID_629374509 A-to-I Human chr17 - 61791708 61791707 61791708 TGGAGGCTCTCTTGGCACTGGGCTGTACTTCCATGGGGCAGGGGTGATGTAGGTAATATGAAACT TGGAGGCTCTCTTGGCACTGGGCTGTACTTCC_TGGGGCAGGGGTGATGTAGGTAATATGAAACT AT A BRIP1 Ensembl:ENSG00000136492 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1184768803 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_6628537,Human_RBP_ID_9873903,Human_RBP_ID_13116467 RMVar_hsa_circ_40097,RMVar_hsa_circ_186032,RMVar_hsa_circ_296404,RMVar_hsa_circ_331137,RMVar_hsa_circ_96568,RMVar_hsa_circ_42812,RMVar_hsa_circ_70611,RMVar_hsa_circ_340649,RMVar_hsa_circ_360154,RMVar_hsa_circ_338801,RMVar_hsa_circ_321145,RMVar_hsa_circ_347800,RMVar_hsa_circ_363818,RMVar_hsa_circ_346003,RMVar_hsa_circ_333198,RMVar_hsa_circ_92865,RMVar_hsa_circ_18542,RMVar_hsa_circ_186039,RMVar_hsa_circ_275989,RMVar_hsa_circ_65119,RMVar_hsa_circ_186033,RMVar_hsa_circ_186034,RMVar_hsa_circ_69229,RMVar_hsa_circ_295911,RMVar_hsa_circ_320794,RMVar_hsa_circ_308778,RMVar_hsa_circ_287108,RMVar_hsa_circ_288036,RMVar_hsa_circ_63938,RMVar_hsa_circ_275035,RMVar_hsa_circ_81566,RMVar_hsa_circ_186043,RMVar_hsa_circ_186041,RMVar_hsa_circ_186042,RMVar_hsa_circ_186040,RMVar_hsa_circ_9922,RMVar_hsa_circ_186038,RMVar_hsa_circ_264785,RMVar_hsa_circ_112995,RMVar_hsa_circ_47028,RMVar_hsa_circ_186049,RMVar_hsa_circ_299195,RMVar_hsa_circ_359136,RMVar_hsa_circ_84616,RMVar_hsa_circ_186050,RMVar_hsa_circ_186051,RMVar_hsa_circ_59655 40773 RMVar_ID_40773 Human_SNP_ID_629374510 A-to-I Human chr17 - 61791708 61791708 61791708 TGGAGGCTCTCTTGGCACTGGGCTGTACTTCCATGGGGCAGGGGTGATGTAGGTAATATGAAACT TGGAGGCTCTCTTGGCACTGGGCTGTACTTCCTTGGGGCAGGGGTGATGTAGGTAATATGAAACT T A BRIP1 Ensembl:ENSG00000136492 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7213329 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6628537,Human_RBP_ID_9873903,Human_RBP_ID_13116467 GWAS_ID_4772 RMVar_hsa_circ_40097,RMVar_hsa_circ_186032,RMVar_hsa_circ_296404,RMVar_hsa_circ_331137,RMVar_hsa_circ_96568,RMVar_hsa_circ_42812,RMVar_hsa_circ_70611,RMVar_hsa_circ_340649,RMVar_hsa_circ_360154,RMVar_hsa_circ_338801,RMVar_hsa_circ_321145,RMVar_hsa_circ_347800,RMVar_hsa_circ_363818,RMVar_hsa_circ_346003,RMVar_hsa_circ_333198,RMVar_hsa_circ_92865,RMVar_hsa_circ_18542,RMVar_hsa_circ_186039,RMVar_hsa_circ_275989,RMVar_hsa_circ_65119,RMVar_hsa_circ_186033,RMVar_hsa_circ_186034,RMVar_hsa_circ_69229,RMVar_hsa_circ_295911,RMVar_hsa_circ_320794,RMVar_hsa_circ_308778,RMVar_hsa_circ_287108,RMVar_hsa_circ_288036,RMVar_hsa_circ_63938,RMVar_hsa_circ_275035,RMVar_hsa_circ_81566,RMVar_hsa_circ_186043,RMVar_hsa_circ_186041,RMVar_hsa_circ_186042,RMVar_hsa_circ_186040,RMVar_hsa_circ_9922,RMVar_hsa_circ_186038,RMVar_hsa_circ_264785,RMVar_hsa_circ_112995,RMVar_hsa_circ_47028,RMVar_hsa_circ_186049,RMVar_hsa_circ_299195,RMVar_hsa_circ_359136,RMVar_hsa_circ_84616,RMVar_hsa_circ_186050,RMVar_hsa_circ_186051,RMVar_hsa_circ_59655 40774 RMVar_ID_40774 Human_SNP_ID_629374511 A-to-I Human chr17 - 61791708 61791708 61791708 TGGAGGCTCTCTTGGCACTGGGCTGTACTTCCATGGGGCAGGGGTGATGTAGGTAATATGAAACT TGGAGGCTCTCTTGGCACTGGGCTGTACTTCCGTGGGGCAGGGGTGATGTAGGTAATATGAAACT T C BRIP1 Ensembl:ENSG00000136492 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7213329 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6628537,Human_RBP_ID_9873903,Human_RBP_ID_13116467 GWAS_ID_4772 RMVar_hsa_circ_40097,RMVar_hsa_circ_186032,RMVar_hsa_circ_296404,RMVar_hsa_circ_331137,RMVar_hsa_circ_96568,RMVar_hsa_circ_42812,RMVar_hsa_circ_70611,RMVar_hsa_circ_340649,RMVar_hsa_circ_360154,RMVar_hsa_circ_338801,RMVar_hsa_circ_321145,RMVar_hsa_circ_347800,RMVar_hsa_circ_363818,RMVar_hsa_circ_346003,RMVar_hsa_circ_333198,RMVar_hsa_circ_92865,RMVar_hsa_circ_18542,RMVar_hsa_circ_186039,RMVar_hsa_circ_275989,RMVar_hsa_circ_65119,RMVar_hsa_circ_186033,RMVar_hsa_circ_186034,RMVar_hsa_circ_69229,RMVar_hsa_circ_295911,RMVar_hsa_circ_320794,RMVar_hsa_circ_308778,RMVar_hsa_circ_287108,RMVar_hsa_circ_288036,RMVar_hsa_circ_63938,RMVar_hsa_circ_275035,RMVar_hsa_circ_81566,RMVar_hsa_circ_186043,RMVar_hsa_circ_186041,RMVar_hsa_circ_186042,RMVar_hsa_circ_186040,RMVar_hsa_circ_9922,RMVar_hsa_circ_186038,RMVar_hsa_circ_264785,RMVar_hsa_circ_112995,RMVar_hsa_circ_47028,RMVar_hsa_circ_186049,RMVar_hsa_circ_299195,RMVar_hsa_circ_359136,RMVar_hsa_circ_84616,RMVar_hsa_circ_186050,RMVar_hsa_circ_186051,RMVar_hsa_circ_59655 40775 RMVar_ID_40775 Human_SNP_ID_629374611 A-to-I Human chr17 - 61792188 61792188 61792188 TAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAAGATTGCTTGAACCCAGGAATTTGAGGCTGTAG TAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGGATTGCTTGAACCCAGGAATTTGAGGCTGTAG T C BRIP1 Ensembl:ENSG00000136492 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1204559757 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13116485 RMVar_hsa_circ_40097,RMVar_hsa_circ_186032,RMVar_hsa_circ_296404,RMVar_hsa_circ_331137,RMVar_hsa_circ_96568,RMVar_hsa_circ_42812,RMVar_hsa_circ_70611,RMVar_hsa_circ_340649,RMVar_hsa_circ_360154,RMVar_hsa_circ_338801,RMVar_hsa_circ_321145,RMVar_hsa_circ_347800,RMVar_hsa_circ_363818,RMVar_hsa_circ_346003,RMVar_hsa_circ_333198,RMVar_hsa_circ_92865,RMVar_hsa_circ_18542,RMVar_hsa_circ_186039,RMVar_hsa_circ_275989,RMVar_hsa_circ_65119,RMVar_hsa_circ_186033,RMVar_hsa_circ_186034,RMVar_hsa_circ_69229,RMVar_hsa_circ_295911,RMVar_hsa_circ_320794,RMVar_hsa_circ_308778,RMVar_hsa_circ_287108,RMVar_hsa_circ_288036,RMVar_hsa_circ_63938,RMVar_hsa_circ_275035,RMVar_hsa_circ_81566,RMVar_hsa_circ_186043,RMVar_hsa_circ_186041,RMVar_hsa_circ_186042,RMVar_hsa_circ_186040,RMVar_hsa_circ_9922,RMVar_hsa_circ_186038,RMVar_hsa_circ_264785,RMVar_hsa_circ_112995,RMVar_hsa_circ_47028,RMVar_hsa_circ_186049,RMVar_hsa_circ_299195,RMVar_hsa_circ_359136,RMVar_hsa_circ_84616,RMVar_hsa_circ_186050,RMVar_hsa_circ_186051,RMVar_hsa_circ_59655 40776 RMVar_ID_40776 Human_SNP_ID_629382330 A-to-I Human chr17 - 61828122 61828122 61828122 TGGGTTGTTTCCATCTTTTTGCTATTTTGAATAATGCTGCTGTGAACATTGGTGTACGTATCTGT TGGGTTGTTTCCATCTTTTTGCTATTTTGAATTATGCTGCTGTGAACATTGGTGTACGTATCTGT T A BRIP1 Ensembl:ENSG00000136492 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270253857 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_186032,RMVar_hsa_circ_296404,RMVar_hsa_circ_96568,RMVar_hsa_circ_360154,RMVar_hsa_circ_338801,RMVar_hsa_circ_333198,RMVar_hsa_circ_92865,RMVar_hsa_circ_18542,RMVar_hsa_circ_186039,RMVar_hsa_circ_275989,RMVar_hsa_circ_65119,RMVar_hsa_circ_186033,RMVar_hsa_circ_295911,RMVar_hsa_circ_287108,RMVar_hsa_circ_63938,RMVar_hsa_circ_81566,RMVar_hsa_circ_186040,RMVar_hsa_circ_186038,RMVar_hsa_circ_112995,RMVar_hsa_circ_47028,RMVar_hsa_circ_186049,RMVar_hsa_circ_359136,RMVar_hsa_circ_11404,RMVar_hsa_circ_362930,RMVar_hsa_circ_68390,RMVar_hsa_circ_54244,RMVar_hsa_circ_265178 40777 RMVar_ID_40777 Human_SNP_ID_629395401 A-to-I Human chr17 - 61885796 61885796 61885796 TGAACCTGGGAGGCAGAGTTTGCAGTGAGCCAAGATCGCGCCACTGCACTCCAGCCTGGTGACAG TGAACCTGGGAGGCAGAGTTTGCAGTGAGCCACGATCGCGCCACTGCACTCCAGCCTGGTGACAG T G INTS2 Ensembl:ENSG00000108506 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1567896011 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7440,RMVar_hsa_circ_89468,RMVar_hsa_circ_99041,RMVar_hsa_circ_105095,RMVar_hsa_circ_186060,RMVar_hsa_circ_186061,RMVar_hsa_circ_83754,RMVar_hsa_circ_109777,RMVar_hsa_circ_186062,RMVar_hsa_circ_186063,RMVar_hsa_circ_106482,RMVar_hsa_circ_186066,RMVar_hsa_circ_85618,RMVar_hsa_circ_186064,RMVar_hsa_circ_186065,RMVar_hsa_circ_124555,RMVar_hsa_circ_186067,RMVar_hsa_circ_77601,RMVar_hsa_circ_63507,RMVar_hsa_circ_94658,RMVar_hsa_circ_186068,RMVar_hsa_circ_56719,RMVar_hsa_circ_275193,RMVar_hsa_circ_186069,RMVar_hsa_circ_325601,RMVar_hsa_circ_279669,RMVar_hsa_circ_91388,RMVar_hsa_circ_32449,RMVar_hsa_circ_48780,RMVar_hsa_circ_186070,RMVar_hsa_circ_186071,RMVar_hsa_circ_304168,RMVar_hsa_circ_348975,RMVar_hsa_circ_378124,RMVar_hsa_circ_59155,RMVar_hsa_circ_186077,RMVar_hsa_circ_186073,RMVar_hsa_circ_186074,RMVar_hsa_circ_186075,RMVar_hsa_circ_117112,RMVar_hsa_circ_113420,RMVar_hsa_circ_284090,RMVar_hsa_circ_186076,RMVar_hsa_circ_336969,RMVar_hsa_circ_279667,RMVar_hsa_circ_109021,RMVar_hsa_circ_186079,RMVar_hsa_circ_186081,RMVar_hsa_circ_13485,RMVar_hsa_circ_186080,RMVar_hsa_circ_186078 40778 RMVar_ID_40778 Human_SNP_ID_629395529 A-to-I Human chr17 - 61886278 61886278 61886278 GGAATGCTGGGGCTGGTGGATCACCTGAGGTCAGGAGTTTGAGACCAGCCTGGCCAATATGGCGA GGAATGCTGGGGCTGGTGGATCACCTGAGGTCGGGAGTTTGAGACCAGCCTGGCCAATATGGCGA T C INTS2 Ensembl:ENSG00000108506 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1458283027 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7440,RMVar_hsa_circ_89468,RMVar_hsa_circ_99041,RMVar_hsa_circ_105095,RMVar_hsa_circ_186060,RMVar_hsa_circ_186061,RMVar_hsa_circ_83754,RMVar_hsa_circ_109777,RMVar_hsa_circ_186062,RMVar_hsa_circ_186063,RMVar_hsa_circ_106482,RMVar_hsa_circ_186066,RMVar_hsa_circ_85618,RMVar_hsa_circ_186064,RMVar_hsa_circ_186065,RMVar_hsa_circ_124555,RMVar_hsa_circ_186067,RMVar_hsa_circ_77601,RMVar_hsa_circ_63507,RMVar_hsa_circ_94658,RMVar_hsa_circ_186068,RMVar_hsa_circ_56719,RMVar_hsa_circ_275193,RMVar_hsa_circ_186069,RMVar_hsa_circ_325601,RMVar_hsa_circ_279669,RMVar_hsa_circ_91388,RMVar_hsa_circ_32449,RMVar_hsa_circ_48780,RMVar_hsa_circ_186070,RMVar_hsa_circ_186071,RMVar_hsa_circ_304168,RMVar_hsa_circ_348975,RMVar_hsa_circ_378124,RMVar_hsa_circ_59155,RMVar_hsa_circ_186077,RMVar_hsa_circ_186073,RMVar_hsa_circ_186074,RMVar_hsa_circ_186075,RMVar_hsa_circ_117112,RMVar_hsa_circ_113420,RMVar_hsa_circ_284090,RMVar_hsa_circ_186076,RMVar_hsa_circ_336969,RMVar_hsa_circ_279667,RMVar_hsa_circ_109021,RMVar_hsa_circ_186079,RMVar_hsa_circ_186081,RMVar_hsa_circ_13485,RMVar_hsa_circ_186080,RMVar_hsa_circ_186078 40779 RMVar_ID_40779 Human_SNP_ID_629398570 A-to-I Human chr17 - 61898373 61898373 61898373 GGAGGATCACTTGAGCTTGGGTGGTCGAGGCTATAGTGAGCTATGATTGCGCCACTGCACTCCAG GGAGGATCACTTGAGCTTGGGTGGTCGAGGCTGTAGTGAGCTATGATTGCGCCACTGCACTCCAG T C INTS2 Ensembl:ENSG00000108506 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1026963894 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89468,RMVar_hsa_circ_99041,RMVar_hsa_circ_105095,RMVar_hsa_circ_186060,RMVar_hsa_circ_186061,RMVar_hsa_circ_83754,RMVar_hsa_circ_109777,RMVar_hsa_circ_186062,RMVar_hsa_circ_186063,RMVar_hsa_circ_106482,RMVar_hsa_circ_186066,RMVar_hsa_circ_85618,RMVar_hsa_circ_186064,RMVar_hsa_circ_186065,RMVar_hsa_circ_124555,RMVar_hsa_circ_186067,RMVar_hsa_circ_77601,RMVar_hsa_circ_94658,RMVar_hsa_circ_186068,RMVar_hsa_circ_186069,RMVar_hsa_circ_91388,RMVar_hsa_circ_32449,RMVar_hsa_circ_186070,RMVar_hsa_circ_304168,RMVar_hsa_circ_348975,RMVar_hsa_circ_186077,RMVar_hsa_circ_186074,RMVar_hsa_circ_186075,RMVar_hsa_circ_113420,RMVar_hsa_circ_284090,RMVar_hsa_circ_279667,RMVar_hsa_circ_109021,RMVar_hsa_circ_186084,RMVar_hsa_circ_305333,RMVar_hsa_circ_186079,RMVar_hsa_circ_186081,RMVar_hsa_circ_13485,RMVar_hsa_circ_186080,RMVar_hsa_circ_314752,RMVar_hsa_circ_22891,RMVar_hsa_circ_102517,RMVar_hsa_circ_30764,RMVar_hsa_circ_6826,RMVar_hsa_circ_186082,RMVar_hsa_circ_186083,RMVar_hsa_circ_309351,RMVar_hsa_circ_14229,RMVar_hsa_circ_89966,RMVar_hsa_circ_50323,RMVar_hsa_circ_186090,RMVar_hsa_circ_335256,RMVar_hsa_circ_186091,RMVar_hsa_circ_92103,RMVar_hsa_circ_186092,RMVar_hsa_circ_44095,RMVar_hsa_circ_186093,RMVar_hsa_circ_343197,RMVar_hsa_circ_95873,RMVar_hsa_circ_78603,RMVar_hsa_circ_186094,RMVar_hsa_circ_186095,RMVar_hsa_circ_186097 40780 RMVar_ID_40780 Human_SNP_ID_629414299 A-to-I Human chr17 - 61955198 61955198 61955198 CTCAATTACGCAGGTGGGCCCTTAATGCGATAACATGTGTTCTTATAAGAAGGAGGCAGAAGGAG CTCAATTACGCAGGTGGGCCCTTAATGCGATAGCATGTGTTCTTATAAGAAGGAGGCAGAAGGAG T C MED13 Ensembl:ENSG00000108510 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1214555388 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93498,RMVar_hsa_circ_104817,RMVar_hsa_circ_268386,RMVar_hsa_circ_323749,RMVar_hsa_circ_335521,RMVar_hsa_circ_360328,RMVar_hsa_circ_186111,RMVar_hsa_circ_373939,RMVar_hsa_circ_355875,RMVar_hsa_circ_330876,RMVar_hsa_circ_267412,RMVar_hsa_circ_306078,RMVar_hsa_circ_102993,RMVar_hsa_circ_55531,RMVar_hsa_circ_186112,RMVar_hsa_circ_186114,RMVar_hsa_circ_186116,RMVar_hsa_circ_186117,RMVar_hsa_circ_186115,RMVar_hsa_circ_186113,RMVar_hsa_circ_265044,RMVar_hsa_circ_304220,RMVar_hsa_circ_309704,RMVar_hsa_circ_266489,RMVar_hsa_circ_59507,RMVar_hsa_circ_186119,RMVar_hsa_circ_186118 40781 RMVar_ID_40781 Human_SNP_ID_629414316 A-to-I Human chr17 - 61955261 61955261 61955261 GTTTTACCAAAAAATGATTTTGCAGATGTGATAAGTTAAGGATCTTGAGATGGAGAGATTATCCT GTTTTACCAAAAAATGATTTTGCAGATGTGATGAGTTAAGGATCTTGAGATGGAGAGATTATCCT T C MED13 Ensembl:ENSG00000108510 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs570825618 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17566550 RMVar_hsa_circ_93498,RMVar_hsa_circ_104817,RMVar_hsa_circ_268386,RMVar_hsa_circ_323749,RMVar_hsa_circ_335521,RMVar_hsa_circ_360328,RMVar_hsa_circ_186111,RMVar_hsa_circ_373939,RMVar_hsa_circ_355875,RMVar_hsa_circ_330876,RMVar_hsa_circ_267412,RMVar_hsa_circ_306078,RMVar_hsa_circ_102993,RMVar_hsa_circ_55531,RMVar_hsa_circ_186112,RMVar_hsa_circ_186114,RMVar_hsa_circ_186116,RMVar_hsa_circ_186117,RMVar_hsa_circ_186115,RMVar_hsa_circ_186113,RMVar_hsa_circ_265044,RMVar_hsa_circ_304220,RMVar_hsa_circ_309704,RMVar_hsa_circ_266489,RMVar_hsa_circ_59507,RMVar_hsa_circ_186119,RMVar_hsa_circ_186118 40782 RMVar_ID_40782 Human_SNP_ID_629418232 A-to-I Human chr17 - 61968464 61968464 61968464 AAAATTAGCCAGGCGTGGTGGCAGGCACTTGCAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAAA AAAATTAGCCAGGCGTGGTGGCAGGCACTTGCGGTCCCAGCTACTCAGGAGGCTGAGGCAGGAAA T C MED13 Ensembl:ENSG00000108510 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1187502697 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85045,RMVar_hsa_circ_104817,RMVar_hsa_circ_323749,RMVar_hsa_circ_360328,RMVar_hsa_circ_186111,RMVar_hsa_circ_373939,RMVar_hsa_circ_267412,RMVar_hsa_circ_186112,RMVar_hsa_circ_309704,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_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_186128,RMVar_hsa_circ_186129,RMVar_hsa_circ_186127,RMVar_hsa_circ_186132,RMVar_hsa_circ_120621,RMVar_hsa_circ_369050,RMVar_hsa_circ_292616,RMVar_hsa_circ_186133,RMVar_hsa_circ_280719,RMVar_hsa_circ_281974,RMVar_hsa_circ_101240,RMVar_hsa_circ_121360,RMVar_hsa_circ_186136,RMVar_hsa_circ_50231,RMVar_hsa_circ_77400,RMVar_hsa_circ_186138,RMVar_hsa_circ_186139,RMVar_hsa_circ_186137,RMVar_hsa_circ_186135,RMVar_hsa_circ_186140,RMVar_hsa_circ_89268,RMVar_hsa_circ_348903,RMVar_hsa_circ_186141,RMVar_hsa_circ_74399,RMVar_hsa_circ_112045,RMVar_hsa_circ_186142 40783 RMVar_ID_40783 Human_SNP_ID_629418332 A-to-I Human chr17 - 61968906 61968906 61968906 CTCTACAAAAACTTTAAAAATTAGCTAAGCATAGTGGCACACACCTGTAGTCCCAGCTATTCGGG CTCTACAAAAACTTTAAAAATTAGCTAAGCATGGTGGCACACACCTGTAGTCCCAGCTATTCGGG T C MED13 Ensembl:ENSG00000108510 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1440660993 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13119555,Human_RBP_ID_17566551 RMVar_hsa_circ_85045,RMVar_hsa_circ_104817,RMVar_hsa_circ_323749,RMVar_hsa_circ_360328,RMVar_hsa_circ_186111,RMVar_hsa_circ_373939,RMVar_hsa_circ_267412,RMVar_hsa_circ_186112,RMVar_hsa_circ_309704,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_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_186128,RMVar_hsa_circ_186129,RMVar_hsa_circ_186127,RMVar_hsa_circ_186132,RMVar_hsa_circ_120621,RMVar_hsa_circ_369050,RMVar_hsa_circ_292616,RMVar_hsa_circ_186133,RMVar_hsa_circ_280719,RMVar_hsa_circ_281974,RMVar_hsa_circ_101240,RMVar_hsa_circ_121360,RMVar_hsa_circ_186136,RMVar_hsa_circ_50231,RMVar_hsa_circ_77400,RMVar_hsa_circ_186138,RMVar_hsa_circ_186139,RMVar_hsa_circ_186137,RMVar_hsa_circ_186135,RMVar_hsa_circ_186140,RMVar_hsa_circ_89268,RMVar_hsa_circ_348903,RMVar_hsa_circ_186141,RMVar_hsa_circ_74399,RMVar_hsa_circ_112045,RMVar_hsa_circ_186142 40784 RMVar_ID_40784 Human_SNP_ID_629418400 A-to-I Human chr17 - 61969193 61969193 61969193 GCACCACCATGCCCGGCTAATTTTGTATTTTTAATAGAGACAGGCTTTCTCCATGTTGGTCAGGC GCACCACCATGCCCGGCTAATTTTGTATTTTTGATAGAGACAGGCTTTCTCCATGTTGGTCAGGC T C MED13 Ensembl:ENSG00000108510 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1020566550 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13119556 RMVar_hsa_circ_85045,RMVar_hsa_circ_104817,RMVar_hsa_circ_323749,RMVar_hsa_circ_360328,RMVar_hsa_circ_186111,RMVar_hsa_circ_373939,RMVar_hsa_circ_267412,RMVar_hsa_circ_186112,RMVar_hsa_circ_309704,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_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_186128,RMVar_hsa_circ_186129,RMVar_hsa_circ_186127,RMVar_hsa_circ_186132,RMVar_hsa_circ_120621,RMVar_hsa_circ_369050,RMVar_hsa_circ_292616,RMVar_hsa_circ_186133,RMVar_hsa_circ_280719,RMVar_hsa_circ_281974,RMVar_hsa_circ_101240,RMVar_hsa_circ_121360,RMVar_hsa_circ_186136,RMVar_hsa_circ_50231,RMVar_hsa_circ_77400,RMVar_hsa_circ_186138,RMVar_hsa_circ_186139,RMVar_hsa_circ_186137,RMVar_hsa_circ_186135,RMVar_hsa_circ_186140,RMVar_hsa_circ_89268,RMVar_hsa_circ_348903,RMVar_hsa_circ_186141,RMVar_hsa_circ_74399,RMVar_hsa_circ_112045,RMVar_hsa_circ_186142 40785 RMVar_ID_40785 Human_SNP_ID_629418401 A-to-I Human chr17 - 61969193 61969193 61969193 GCACCACCATGCCCGGCTAATTTTGTATTTTTAATAGAGACAGGCTTTCTCCATGTTGGTCAGGC GCACCACCATGCCCGGCTAATTTTGTATTTTTCATAGAGACAGGCTTTCTCCATGTTGGTCAGGC T G MED13 Ensembl:ENSG00000108510 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1020566550 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13119556 RMVar_hsa_circ_85045,RMVar_hsa_circ_104817,RMVar_hsa_circ_323749,RMVar_hsa_circ_360328,RMVar_hsa_circ_186111,RMVar_hsa_circ_373939,RMVar_hsa_circ_267412,RMVar_hsa_circ_186112,RMVar_hsa_circ_309704,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_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_186128,RMVar_hsa_circ_186129,RMVar_hsa_circ_186127,RMVar_hsa_circ_186132,RMVar_hsa_circ_120621,RMVar_hsa_circ_369050,RMVar_hsa_circ_292616,RMVar_hsa_circ_186133,RMVar_hsa_circ_280719,RMVar_hsa_circ_281974,RMVar_hsa_circ_101240,RMVar_hsa_circ_121360,RMVar_hsa_circ_186136,RMVar_hsa_circ_50231,RMVar_hsa_circ_77400,RMVar_hsa_circ_186138,RMVar_hsa_circ_186139,RMVar_hsa_circ_186137,RMVar_hsa_circ_186135,RMVar_hsa_circ_186140,RMVar_hsa_circ_89268,RMVar_hsa_circ_348903,RMVar_hsa_circ_186141,RMVar_hsa_circ_74399,RMVar_hsa_circ_112045,RMVar_hsa_circ_186142 40786 RMVar_ID_40786 Human_SNP_ID_629418434 A-to-I Human chr17 - 61969289 61969289 61969289 GACGTGCACTGGTGCAATCTCAGCTCACCGCAACCTCCACCCCCTGGGTTCAAGCAATTCTGCTT GACGTGCACTGGTGCAATCTCAGCTCACCGCAGCCTCCACCCCCTGGGTTCAAGCAATTCTGCTT T C MED13 Ensembl:ENSG00000108510 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs899572627 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85045,RMVar_hsa_circ_104817,RMVar_hsa_circ_323749,RMVar_hsa_circ_360328,RMVar_hsa_circ_186111,RMVar_hsa_circ_373939,RMVar_hsa_circ_267412,RMVar_hsa_circ_186112,RMVar_hsa_circ_309704,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_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_186128,RMVar_hsa_circ_186129,RMVar_hsa_circ_186127,RMVar_hsa_circ_186132,RMVar_hsa_circ_120621,RMVar_hsa_circ_369050,RMVar_hsa_circ_292616,RMVar_hsa_circ_186133,RMVar_hsa_circ_280719,RMVar_hsa_circ_281974,RMVar_hsa_circ_101240,RMVar_hsa_circ_121360,RMVar_hsa_circ_186136,RMVar_hsa_circ_50231,RMVar_hsa_circ_77400,RMVar_hsa_circ_186138,RMVar_hsa_circ_186139,RMVar_hsa_circ_186137,RMVar_hsa_circ_186135,RMVar_hsa_circ_186140,RMVar_hsa_circ_89268,RMVar_hsa_circ_348903,RMVar_hsa_circ_186141,RMVar_hsa_circ_74399,RMVar_hsa_circ_112045,RMVar_hsa_circ_186142 40787 RMVar_ID_40787 Human_SNP_ID_629418438 A-to-I Human chr17 - 61969295 61969295 61969295 TGGGCTGACGTGCACTGGTGCAATCTCAGCTCACCGCAACCTCCACCCCCTGGGTTCAAGCAATT TGGGCTGACGTGCACTGGTGCAATCTCAGCTCCCCGCAACCTCCACCCCCTGGGTTCAAGCAATT T G MED13 Ensembl:ENSG00000108510 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs539034003 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85045,RMVar_hsa_circ_104817,RMVar_hsa_circ_323749,RMVar_hsa_circ_360328,RMVar_hsa_circ_186111,RMVar_hsa_circ_373939,RMVar_hsa_circ_267412,RMVar_hsa_circ_186112,RMVar_hsa_circ_309704,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_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_186128,RMVar_hsa_circ_186129,RMVar_hsa_circ_186127,RMVar_hsa_circ_186132,RMVar_hsa_circ_120621,RMVar_hsa_circ_369050,RMVar_hsa_circ_292616,RMVar_hsa_circ_186133,RMVar_hsa_circ_280719,RMVar_hsa_circ_281974,RMVar_hsa_circ_101240,RMVar_hsa_circ_121360,RMVar_hsa_circ_186136,RMVar_hsa_circ_50231,RMVar_hsa_circ_77400,RMVar_hsa_circ_186138,RMVar_hsa_circ_186139,RMVar_hsa_circ_186137,RMVar_hsa_circ_186135,RMVar_hsa_circ_186140,RMVar_hsa_circ_89268,RMVar_hsa_circ_348903,RMVar_hsa_circ_186141,RMVar_hsa_circ_74399,RMVar_hsa_circ_112045,RMVar_hsa_circ_186142 40788 RMVar_ID_40788 Human_SNP_ID_629418442 A-to-I Human chr17 - 61969306 61969306 61969306 CTCTTTTTGCCTGGGCTGACGTGCACTGGTGCAATCTCAGCTCACCGCAACCTCCACCCCCTGGG CTCTTTTTGCCTGGGCTGACGTGCACTGGTGCCATCTCAGCTCACCGCAACCTCCACCCCCTGGG T G MED13 Ensembl:ENSG00000108510 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1193819754 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85045,RMVar_hsa_circ_104817,RMVar_hsa_circ_323749,RMVar_hsa_circ_360328,RMVar_hsa_circ_186111,RMVar_hsa_circ_373939,RMVar_hsa_circ_267412,RMVar_hsa_circ_186112,RMVar_hsa_circ_309704,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_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_186128,RMVar_hsa_circ_186129,RMVar_hsa_circ_186127,RMVar_hsa_circ_186132,RMVar_hsa_circ_120621,RMVar_hsa_circ_369050,RMVar_hsa_circ_292616,RMVar_hsa_circ_186133,RMVar_hsa_circ_280719,RMVar_hsa_circ_281974,RMVar_hsa_circ_101240,RMVar_hsa_circ_121360,RMVar_hsa_circ_186136,RMVar_hsa_circ_50231,RMVar_hsa_circ_77400,RMVar_hsa_circ_186138,RMVar_hsa_circ_186139,RMVar_hsa_circ_186137,RMVar_hsa_circ_186135,RMVar_hsa_circ_186140,RMVar_hsa_circ_89268,RMVar_hsa_circ_348903,RMVar_hsa_circ_186141,RMVar_hsa_circ_74399,RMVar_hsa_circ_112045,RMVar_hsa_circ_186142 40789 RMVar_ID_40789 Human_SNP_ID_629418572 A-to-I Human chr17 - 61969742 61969742 61969742 CAAAAATTATCCCGGTATGGTGATGTGTGCCTATAATCCCAGCTACTCAGGAGGCTGAGGTGAGA CAAAAATTATCCCGGTATGGTGATGTGTGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGTGAGA T C MED13 Ensembl:ENSG00000108510 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1289337730 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85045,RMVar_hsa_circ_104817,RMVar_hsa_circ_323749,RMVar_hsa_circ_360328,RMVar_hsa_circ_186111,RMVar_hsa_circ_373939,RMVar_hsa_circ_267412,RMVar_hsa_circ_186112,RMVar_hsa_circ_309704,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_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_186128,RMVar_hsa_circ_186129,RMVar_hsa_circ_186127,RMVar_hsa_circ_186132,RMVar_hsa_circ_120621,RMVar_hsa_circ_369050,RMVar_hsa_circ_292616,RMVar_hsa_circ_186133,RMVar_hsa_circ_280719,RMVar_hsa_circ_281974,RMVar_hsa_circ_101240,RMVar_hsa_circ_121360,RMVar_hsa_circ_186136,RMVar_hsa_circ_50231,RMVar_hsa_circ_77400,RMVar_hsa_circ_186138,RMVar_hsa_circ_186139,RMVar_hsa_circ_186137,RMVar_hsa_circ_186135,RMVar_hsa_circ_186140,RMVar_hsa_circ_89268,RMVar_hsa_circ_348903,RMVar_hsa_circ_186141,RMVar_hsa_circ_74399,RMVar_hsa_circ_112045,RMVar_hsa_circ_186142 40790 RMVar_ID_40790 Human_SNP_ID_629418575 A-to-I Human chr17 - 61969758 61969758 61969758 ATCTCTACCAAAAATTCAAAAATTATCCCGGTATGGTGATGTGTGCCTATAATCCCAGCTACTCA ATCTCTACCAAAAATTCAAAAATTATCCCGGTGTGGTGATGTGTGCCTATAATCCCAGCTACTCA T C MED13 Ensembl:ENSG00000108510 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1172823771 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85045,RMVar_hsa_circ_104817,RMVar_hsa_circ_323749,RMVar_hsa_circ_360328,RMVar_hsa_circ_186111,RMVar_hsa_circ_373939,RMVar_hsa_circ_267412,RMVar_hsa_circ_186112,RMVar_hsa_circ_309704,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_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_186128,RMVar_hsa_circ_186129,RMVar_hsa_circ_186127,RMVar_hsa_circ_186132,RMVar_hsa_circ_120621,RMVar_hsa_circ_369050,RMVar_hsa_circ_292616,RMVar_hsa_circ_186133,RMVar_hsa_circ_280719,RMVar_hsa_circ_281974,RMVar_hsa_circ_101240,RMVar_hsa_circ_121360,RMVar_hsa_circ_186136,RMVar_hsa_circ_50231,RMVar_hsa_circ_77400,RMVar_hsa_circ_186138,RMVar_hsa_circ_186139,RMVar_hsa_circ_186137,RMVar_hsa_circ_186135,RMVar_hsa_circ_186140,RMVar_hsa_circ_89268,RMVar_hsa_circ_348903,RMVar_hsa_circ_186141,RMVar_hsa_circ_74399,RMVar_hsa_circ_112045,RMVar_hsa_circ_186142 40791 RMVar_ID_40791 Human_SNP_ID_629421079 A-to-I Human chr17 - 61979381 61979381 61979381 AGCTTGAACCTAGGAGGTGGAGGATTCGGTGAACCATGATTGTACCACTGCACTCCAGCCTATTT AGCTTGAACCTAGGAGGTGGAGGATTCGGTGAGCCATGATTGTACCACTGCACTCCAGCCTATTT T C MED13 Ensembl:ENSG00000108510 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1437932059 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13119755 RMVar_hsa_circ_85045,RMVar_hsa_circ_104817,RMVar_hsa_circ_323749,RMVar_hsa_circ_186111,RMVar_hsa_circ_373939,RMVar_hsa_circ_267412,RMVar_hsa_circ_186112,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_56064,RMVar_hsa_circ_88424,RMVar_hsa_circ_186125,RMVar_hsa_circ_347960,RMVar_hsa_circ_186126,RMVar_hsa_circ_281878,RMVar_hsa_circ_83249,RMVar_hsa_circ_186128,RMVar_hsa_circ_186127,RMVar_hsa_circ_186132,RMVar_hsa_circ_120621,RMVar_hsa_circ_292616,RMVar_hsa_circ_186133,RMVar_hsa_circ_281974,RMVar_hsa_circ_101240,RMVar_hsa_circ_43065,RMVar_hsa_circ_121360,RMVar_hsa_circ_186136,RMVar_hsa_circ_50231,RMVar_hsa_circ_77400,RMVar_hsa_circ_186138,RMVar_hsa_circ_186139,RMVar_hsa_circ_186137,RMVar_hsa_circ_186140,RMVar_hsa_circ_89268,RMVar_hsa_circ_348903,RMVar_hsa_circ_186141,RMVar_hsa_circ_112045,RMVar_hsa_circ_186142,RMVar_hsa_circ_292494,RMVar_hsa_circ_296669,RMVar_hsa_circ_372759,RMVar_hsa_circ_104772,RMVar_hsa_circ_186143,RMVar_hsa_circ_7213,RMVar_hsa_circ_15533,RMVar_hsa_circ_186145,RMVar_hsa_circ_186146,RMVar_hsa_circ_186147,RMVar_hsa_circ_186144 40792 RMVar_ID_40792 Human_SNP_ID_629423917 A-to-I Human chr17 - 61990264 61990264 61990264 TGTGTATGTATATATAGTGGAATGGGTAGATCAAGCTGTTTAACATATGCATTACCTTACATACC TGTGTATGTATATATAGTGGAATGGGTAGATCGAGCTGTTTAACATATGCATTACCTTACATACC T C MED13 Ensembl:ENSG00000108510 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs949001137 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6629821,Human_RBP_ID_13119984,Human_RBP_ID_17565612,Human_RBP_ID_23741762 RMVar_hsa_circ_85045,RMVar_hsa_circ_104817,RMVar_hsa_circ_186111,RMVar_hsa_circ_267412,RMVar_hsa_circ_119612,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_56064,RMVar_hsa_circ_88424,RMVar_hsa_circ_186125,RMVar_hsa_circ_347960,RMVar_hsa_circ_186126,RMVar_hsa_circ_83249,RMVar_hsa_circ_186127,RMVar_hsa_circ_120621,RMVar_hsa_circ_186133,RMVar_hsa_circ_101240,RMVar_hsa_circ_121360,RMVar_hsa_circ_50231,RMVar_hsa_circ_186138,RMVar_hsa_circ_186139,RMVar_hsa_circ_186140,RMVar_hsa_circ_89268,RMVar_hsa_circ_186141,RMVar_hsa_circ_112045,RMVar_hsa_circ_186142,RMVar_hsa_circ_372759,RMVar_hsa_circ_104772,RMVar_hsa_circ_186143,RMVar_hsa_circ_15533,RMVar_hsa_circ_186145,RMVar_hsa_circ_186144,RMVar_hsa_circ_286182,RMVar_hsa_circ_353824,RMVar_hsa_circ_361895,RMVar_hsa_circ_62540,RMVar_hsa_circ_123911,RMVar_hsa_circ_186151,RMVar_hsa_circ_186152,RMVar_hsa_circ_336303,RMVar_hsa_circ_347973,RMVar_hsa_circ_120286,RMVar_hsa_circ_186155,RMVar_hsa_circ_115950,RMVar_hsa_circ_304263,RMVar_hsa_circ_318987,RMVar_hsa_circ_279047,RMVar_hsa_circ_186157 40793 RMVar_ID_40793 Human_SNP_ID_629426320 A-to-I Human chr17 - 61998798 61998798 61998798 GCCCAGGAGTTCAAGACCAGCCTGGGCAATATAGTGAGATCCTGTCTCTACAAAAAATAAAAAAC GCCCAGGAGTTCAAGACCAGCCTGGGCAATATCGTGAGATCCTGTCTCTACAAAAAATAAAAAAC T G MED13 Ensembl:ENSG00000108510 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1283005414 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10550,RMVar_hsa_circ_85045,RMVar_hsa_circ_104817,RMVar_hsa_circ_186111,RMVar_hsa_circ_119612,RMVar_hsa_circ_81309,RMVar_hsa_circ_110787,RMVar_hsa_circ_102026,RMVar_hsa_circ_186123,RMVar_hsa_circ_186124,RMVar_hsa_circ_186122,RMVar_hsa_circ_88424,RMVar_hsa_circ_186125,RMVar_hsa_circ_186126,RMVar_hsa_circ_83249,RMVar_hsa_circ_186127,RMVar_hsa_circ_120621,RMVar_hsa_circ_186133,RMVar_hsa_circ_101240,RMVar_hsa_circ_121360,RMVar_hsa_circ_50231,RMVar_hsa_circ_186138,RMVar_hsa_circ_186139,RMVar_hsa_circ_186140,RMVar_hsa_circ_89268,RMVar_hsa_circ_186142,RMVar_hsa_circ_372759,RMVar_hsa_circ_104772,RMVar_hsa_circ_186143,RMVar_hsa_circ_186144,RMVar_hsa_circ_353824,RMVar_hsa_circ_361895,RMVar_hsa_circ_62540,RMVar_hsa_circ_123911,RMVar_hsa_circ_186152,RMVar_hsa_circ_336303,RMVar_hsa_circ_120286,RMVar_hsa_circ_186155,RMVar_hsa_circ_304263,RMVar_hsa_circ_279047,RMVar_hsa_circ_290568,RMVar_hsa_circ_355612,RMVar_hsa_circ_96938,RMVar_hsa_circ_186159,RMVar_hsa_circ_22555,RMVar_hsa_circ_298747,RMVar_hsa_circ_186158,RMVar_hsa_circ_284367,RMVar_hsa_circ_186162 40794 RMVar_ID_40794 Human_SNP_ID_629426552 A-to-I Human chr17 - 61999800 61999800 61999800 CTACTACCTTGGCCTCCCAAAGCGCTGGGATTACAGATGTGAGCCACTGCACCCAGCCCTCTTGA CTACTACCTTGGCCTCCCAAAGCGCTGGGATTGCAGATGTGAGCCACTGCACCCAGCCCTCTTGA T C MED13 Ensembl:ENSG00000108510 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1379003594 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10550,RMVar_hsa_circ_85045,RMVar_hsa_circ_104817,RMVar_hsa_circ_186111,RMVar_hsa_circ_119612,RMVar_hsa_circ_81309,RMVar_hsa_circ_110787,RMVar_hsa_circ_102026,RMVar_hsa_circ_186123,RMVar_hsa_circ_186124,RMVar_hsa_circ_186122,RMVar_hsa_circ_88424,RMVar_hsa_circ_186125,RMVar_hsa_circ_186126,RMVar_hsa_circ_83249,RMVar_hsa_circ_186127,RMVar_hsa_circ_120621,RMVar_hsa_circ_186133,RMVar_hsa_circ_101240,RMVar_hsa_circ_121360,RMVar_hsa_circ_50231,RMVar_hsa_circ_186138,RMVar_hsa_circ_186139,RMVar_hsa_circ_186140,RMVar_hsa_circ_89268,RMVar_hsa_circ_186142,RMVar_hsa_circ_372759,RMVar_hsa_circ_104772,RMVar_hsa_circ_186143,RMVar_hsa_circ_186144,RMVar_hsa_circ_353824,RMVar_hsa_circ_361895,RMVar_hsa_circ_62540,RMVar_hsa_circ_123911,RMVar_hsa_circ_186152,RMVar_hsa_circ_336303,RMVar_hsa_circ_120286,RMVar_hsa_circ_186155,RMVar_hsa_circ_304263,RMVar_hsa_circ_279047,RMVar_hsa_circ_290568,RMVar_hsa_circ_355612,RMVar_hsa_circ_96938,RMVar_hsa_circ_186159,RMVar_hsa_circ_22555,RMVar_hsa_circ_298747,RMVar_hsa_circ_186158,RMVar_hsa_circ_284367,RMVar_hsa_circ_186162 40795 RMVar_ID_40795 Human_SNP_ID_629426577 A-to-I Human chr17 - 61999874 61999874 61999874 TTTTTAGCCAGGATTTTAGACAGGATCTCGCTATGTTGTCCAGGCTGGTCTTGAACTCCTGGTCT TTTTTAGCCAGGATTTTAGACAGGATCTCGCTTTGTTGTCCAGGCTGGTCTTGAACTCCTGGTCT T A MED13 Ensembl:ENSG00000108510 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs941094878 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5497513,Human_RBP_ID_13120193 RMVar_hsa_circ_10550,RMVar_hsa_circ_85045,RMVar_hsa_circ_104817,RMVar_hsa_circ_186111,RMVar_hsa_circ_119612,RMVar_hsa_circ_81309,RMVar_hsa_circ_110787,RMVar_hsa_circ_102026,RMVar_hsa_circ_186123,RMVar_hsa_circ_186124,RMVar_hsa_circ_186122,RMVar_hsa_circ_88424,RMVar_hsa_circ_186125,RMVar_hsa_circ_186126,RMVar_hsa_circ_83249,RMVar_hsa_circ_186127,RMVar_hsa_circ_120621,RMVar_hsa_circ_186133,RMVar_hsa_circ_101240,RMVar_hsa_circ_121360,RMVar_hsa_circ_50231,RMVar_hsa_circ_186138,RMVar_hsa_circ_186139,RMVar_hsa_circ_186140,RMVar_hsa_circ_89268,RMVar_hsa_circ_186142,RMVar_hsa_circ_372759,RMVar_hsa_circ_104772,RMVar_hsa_circ_186143,RMVar_hsa_circ_186144,RMVar_hsa_circ_353824,RMVar_hsa_circ_361895,RMVar_hsa_circ_62540,RMVar_hsa_circ_123911,RMVar_hsa_circ_186152,RMVar_hsa_circ_336303,RMVar_hsa_circ_120286,RMVar_hsa_circ_186155,RMVar_hsa_circ_304263,RMVar_hsa_circ_279047,RMVar_hsa_circ_290568,RMVar_hsa_circ_355612,RMVar_hsa_circ_96938,RMVar_hsa_circ_186159,RMVar_hsa_circ_22555,RMVar_hsa_circ_298747,RMVar_hsa_circ_186158,RMVar_hsa_circ_284367,RMVar_hsa_circ_186162 40796 RMVar_ID_40796 Human_SNP_ID_629426578 A-to-I Human chr17 - 61999874 61999874 61999874 TTTTTAGCCAGGATTTTAGACAGGATCTCGCTATGTTGTCCAGGCTGGTCTTGAACTCCTGGTCT TTTTTAGCCAGGATTTTAGACAGGATCTCGCTGTGTTGTCCAGGCTGGTCTTGAACTCCTGGTCT T C MED13 Ensembl:ENSG00000108510 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs941094878 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5497513,Human_RBP_ID_13120193 RMVar_hsa_circ_10550,RMVar_hsa_circ_85045,RMVar_hsa_circ_104817,RMVar_hsa_circ_186111,RMVar_hsa_circ_119612,RMVar_hsa_circ_81309,RMVar_hsa_circ_110787,RMVar_hsa_circ_102026,RMVar_hsa_circ_186123,RMVar_hsa_circ_186124,RMVar_hsa_circ_186122,RMVar_hsa_circ_88424,RMVar_hsa_circ_186125,RMVar_hsa_circ_186126,RMVar_hsa_circ_83249,RMVar_hsa_circ_186127,RMVar_hsa_circ_120621,RMVar_hsa_circ_186133,RMVar_hsa_circ_101240,RMVar_hsa_circ_121360,RMVar_hsa_circ_50231,RMVar_hsa_circ_186138,RMVar_hsa_circ_186139,RMVar_hsa_circ_186140,RMVar_hsa_circ_89268,RMVar_hsa_circ_186142,RMVar_hsa_circ_372759,RMVar_hsa_circ_104772,RMVar_hsa_circ_186143,RMVar_hsa_circ_186144,RMVar_hsa_circ_353824,RMVar_hsa_circ_361895,RMVar_hsa_circ_62540,RMVar_hsa_circ_123911,RMVar_hsa_circ_186152,RMVar_hsa_circ_336303,RMVar_hsa_circ_120286,RMVar_hsa_circ_186155,RMVar_hsa_circ_304263,RMVar_hsa_circ_279047,RMVar_hsa_circ_290568,RMVar_hsa_circ_355612,RMVar_hsa_circ_96938,RMVar_hsa_circ_186159,RMVar_hsa_circ_22555,RMVar_hsa_circ_298747,RMVar_hsa_circ_186158,RMVar_hsa_circ_284367,RMVar_hsa_circ_186162 40797 RMVar_ID_40797 Human_SNP_ID_629426808 A-to-I Human chr17 - 62000825 62000825 62000825 CTGGGAGCCAGAGGTTGCAGTGAGCCAAGACCACGCCACTGCACTCCATCCTGAGCAACAGAGCA CTGGGAGCCAGAGGTTGCAGTGAGCCAAGACCGCGCCACTGCACTCCATCCTGAGCAACAGAGCA T C MED13 Ensembl:ENSG00000108510 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1200954221 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6629939,Human_RBP_ID_9887516,Human_RBP_ID_25345983 RMVar_hsa_circ_10550,RMVar_hsa_circ_85045,RMVar_hsa_circ_104817,RMVar_hsa_circ_186111,RMVar_hsa_circ_119612,RMVar_hsa_circ_81309,RMVar_hsa_circ_110787,RMVar_hsa_circ_102026,RMVar_hsa_circ_186123,RMVar_hsa_circ_186124,RMVar_hsa_circ_186122,RMVar_hsa_circ_88424,RMVar_hsa_circ_186125,RMVar_hsa_circ_186126,RMVar_hsa_circ_83249,RMVar_hsa_circ_186127,RMVar_hsa_circ_120621,RMVar_hsa_circ_186133,RMVar_hsa_circ_101240,RMVar_hsa_circ_121360,RMVar_hsa_circ_50231,RMVar_hsa_circ_186138,RMVar_hsa_circ_186139,RMVar_hsa_circ_186140,RMVar_hsa_circ_89268,RMVar_hsa_circ_186142,RMVar_hsa_circ_372759,RMVar_hsa_circ_104772,RMVar_hsa_circ_186143,RMVar_hsa_circ_186144,RMVar_hsa_circ_353824,RMVar_hsa_circ_361895,RMVar_hsa_circ_62540,RMVar_hsa_circ_123911,RMVar_hsa_circ_186152,RMVar_hsa_circ_336303,RMVar_hsa_circ_120286,RMVar_hsa_circ_186155,RMVar_hsa_circ_304263,RMVar_hsa_circ_279047,RMVar_hsa_circ_290568,RMVar_hsa_circ_355612,RMVar_hsa_circ_96938,RMVar_hsa_circ_186159,RMVar_hsa_circ_22555,RMVar_hsa_circ_298747,RMVar_hsa_circ_186158,RMVar_hsa_circ_284367,RMVar_hsa_circ_186162 40798 RMVar_ID_40798 Human_SNP_ID_629427181 A-to-I Human chr17 - 62002307 62002307 62002307 TTTTTGTATTTTCAGTAGAGACGGGTTTCGCCATGTTGGCCAGGCTGGTCTTGAACTCCCTACCT TTTTTGTATTTTCAGTAGAGACGGGTTTCGCCGTGTTGGCCAGGCTGGTCTTGAACTCCCTACCT T C MED13 Ensembl:ENSG00000108510 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1159934954 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10550,RMVar_hsa_circ_85045,RMVar_hsa_circ_104817,RMVar_hsa_circ_186111,RMVar_hsa_circ_119612,RMVar_hsa_circ_81309,RMVar_hsa_circ_110787,RMVar_hsa_circ_102026,RMVar_hsa_circ_186123,RMVar_hsa_circ_186124,RMVar_hsa_circ_186122,RMVar_hsa_circ_88424,RMVar_hsa_circ_186125,RMVar_hsa_circ_186126,RMVar_hsa_circ_83249,RMVar_hsa_circ_186127,RMVar_hsa_circ_120621,RMVar_hsa_circ_186133,RMVar_hsa_circ_101240,RMVar_hsa_circ_121360,RMVar_hsa_circ_50231,RMVar_hsa_circ_186138,RMVar_hsa_circ_186139,RMVar_hsa_circ_186140,RMVar_hsa_circ_89268,RMVar_hsa_circ_186142,RMVar_hsa_circ_372759,RMVar_hsa_circ_104772,RMVar_hsa_circ_186143,RMVar_hsa_circ_186144,RMVar_hsa_circ_353824,RMVar_hsa_circ_361895,RMVar_hsa_circ_62540,RMVar_hsa_circ_123911,RMVar_hsa_circ_186152,RMVar_hsa_circ_336303,RMVar_hsa_circ_120286,RMVar_hsa_circ_186155,RMVar_hsa_circ_304263,RMVar_hsa_circ_279047,RMVar_hsa_circ_290568,RMVar_hsa_circ_355612,RMVar_hsa_circ_96938,RMVar_hsa_circ_186159,RMVar_hsa_circ_22555,RMVar_hsa_circ_298747,RMVar_hsa_circ_186158,RMVar_hsa_circ_284367,RMVar_hsa_circ_186162 40799 RMVar_ID_40799 Human_SNP_ID_629427995 A-to-I Human chr17 - 62005077 62005077 62005077 CAGCCTGGCCAACATGGTGAAACCCTGTCTCTACTAAAAATACAAAAATTAGCTGGGTGTGGTGG CAGCCTGGCCAACATGGTGAAACCCTGTCTCTGCTAAAAATACAAAAATTAGCTGGGTGTGGTGG T C AC018628.2,MED13 Ensembl:ENSG00000279133,Ensembl:ENSG00000108510 Other,Protein coding exon,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1197591277 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10550,RMVar_hsa_circ_85045,RMVar_hsa_circ_104817,RMVar_hsa_circ_186111,RMVar_hsa_circ_119612,RMVar_hsa_circ_81309,RMVar_hsa_circ_110787,RMVar_hsa_circ_102026,RMVar_hsa_circ_186123,RMVar_hsa_circ_186124,RMVar_hsa_circ_186122,RMVar_hsa_circ_88424,RMVar_hsa_circ_186125,RMVar_hsa_circ_186126,RMVar_hsa_circ_83249,RMVar_hsa_circ_186127,RMVar_hsa_circ_120621,RMVar_hsa_circ_186133,RMVar_hsa_circ_101240,RMVar_hsa_circ_121360,RMVar_hsa_circ_50231,RMVar_hsa_circ_186138,RMVar_hsa_circ_186139,RMVar_hsa_circ_186140,RMVar_hsa_circ_89268,RMVar_hsa_circ_186142,RMVar_hsa_circ_372759,RMVar_hsa_circ_104772,RMVar_hsa_circ_186143,RMVar_hsa_circ_186144,RMVar_hsa_circ_353824,RMVar_hsa_circ_361895,RMVar_hsa_circ_62540,RMVar_hsa_circ_123911,RMVar_hsa_circ_186152,RMVar_hsa_circ_336303,RMVar_hsa_circ_120286,RMVar_hsa_circ_186155,RMVar_hsa_circ_304263,RMVar_hsa_circ_279047,RMVar_hsa_circ_290568,RMVar_hsa_circ_355612,RMVar_hsa_circ_96938,RMVar_hsa_circ_186159,RMVar_hsa_circ_22555,RMVar_hsa_circ_298747,RMVar_hsa_circ_186158,RMVar_hsa_circ_284367,RMVar_hsa_circ_186162 40800 RMVar_ID_40800 Human_SNP_ID_629428068 A-to-I Human chr17 - 62005361 62005361 62005361 TCTCAAGTGATCAGTCTGTGTCAGCCTCCCCAAGTGCTGGGATTACAGACACGAGCCACTCTGCC TCTCAAGTGATCAGTCTGTGTCAGCCTCCCCACGTGCTGGGATTACAGACACGAGCCACTCTGCC T G AC018628.2,MED13 Ensembl:ENSG00000279133,Ensembl:ENSG00000108510 Other,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1322353273 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6630016,Human_RBP_ID_13120432 RMVar_hsa_circ_10550,RMVar_hsa_circ_85045,RMVar_hsa_circ_104817,RMVar_hsa_circ_186111,RMVar_hsa_circ_119612,RMVar_hsa_circ_81309,RMVar_hsa_circ_110787,RMVar_hsa_circ_102026,RMVar_hsa_circ_186123,RMVar_hsa_circ_186124,RMVar_hsa_circ_186122,RMVar_hsa_circ_88424,RMVar_hsa_circ_186125,RMVar_hsa_circ_186126,RMVar_hsa_circ_83249,RMVar_hsa_circ_186127,RMVar_hsa_circ_120621,RMVar_hsa_circ_186133,RMVar_hsa_circ_101240,RMVar_hsa_circ_121360,RMVar_hsa_circ_50231,RMVar_hsa_circ_186138,RMVar_hsa_circ_186139,RMVar_hsa_circ_186140,RMVar_hsa_circ_89268,RMVar_hsa_circ_186142,RMVar_hsa_circ_372759,RMVar_hsa_circ_104772,RMVar_hsa_circ_186143,RMVar_hsa_circ_186144,RMVar_hsa_circ_353824,RMVar_hsa_circ_361895,RMVar_hsa_circ_62540,RMVar_hsa_circ_123911,RMVar_hsa_circ_186152,RMVar_hsa_circ_336303,RMVar_hsa_circ_120286,RMVar_hsa_circ_186155,RMVar_hsa_circ_304263,RMVar_hsa_circ_279047,RMVar_hsa_circ_290568,RMVar_hsa_circ_355612,RMVar_hsa_circ_96938,RMVar_hsa_circ_186159,RMVar_hsa_circ_22555,RMVar_hsa_circ_298747,RMVar_hsa_circ_186158,RMVar_hsa_circ_284367,RMVar_hsa_circ_186162 40801 RMVar_ID_40801 Human_SNP_ID_629428108 A-to-I Human chr17 - 62005505 62005505 62005505 ACCTCCCAGGTTCACGCGATTCTTGTGCCTCAACCTCCAGAATAGCTGGGATTACAGGCGTGCAC ACCTCCCAGGTTCACGCGATTCTTGTGCCTCATCCTCCAGAATAGCTGGGATTACAGGCGTGCAC T A AC018628.2,MED13 Ensembl:ENSG00000279133,Ensembl:ENSG00000108510 Other,Protein coding exon,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1439008052 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10550,RMVar_hsa_circ_85045,RMVar_hsa_circ_104817,RMVar_hsa_circ_186111,RMVar_hsa_circ_119612,RMVar_hsa_circ_81309,RMVar_hsa_circ_110787,RMVar_hsa_circ_102026,RMVar_hsa_circ_186123,RMVar_hsa_circ_186124,RMVar_hsa_circ_186122,RMVar_hsa_circ_88424,RMVar_hsa_circ_186125,RMVar_hsa_circ_186126,RMVar_hsa_circ_83249,RMVar_hsa_circ_186127,RMVar_hsa_circ_120621,RMVar_hsa_circ_186133,RMVar_hsa_circ_101240,RMVar_hsa_circ_121360,RMVar_hsa_circ_50231,RMVar_hsa_circ_186138,RMVar_hsa_circ_186139,RMVar_hsa_circ_186140,RMVar_hsa_circ_89268,RMVar_hsa_circ_186142,RMVar_hsa_circ_372759,RMVar_hsa_circ_104772,RMVar_hsa_circ_186143,RMVar_hsa_circ_186144,RMVar_hsa_circ_353824,RMVar_hsa_circ_361895,RMVar_hsa_circ_62540,RMVar_hsa_circ_123911,RMVar_hsa_circ_186152,RMVar_hsa_circ_336303,RMVar_hsa_circ_120286,RMVar_hsa_circ_186155,RMVar_hsa_circ_304263,RMVar_hsa_circ_279047,RMVar_hsa_circ_290568,RMVar_hsa_circ_355612,RMVar_hsa_circ_96938,RMVar_hsa_circ_186159,RMVar_hsa_circ_22555,RMVar_hsa_circ_298747,RMVar_hsa_circ_186158,RMVar_hsa_circ_284367,RMVar_hsa_circ_186162 40802 RMVar_ID_40802 Human_SNP_ID_629428109 A-to-I Human chr17 - 62005506 62005506 62005506 CACCTCCCAGGTTCACGCGATTCTTGTGCCTCAACCTCCAGAATAGCTGGGATTACAGGCGTGCA CACCTCCCAGGTTCACGCGATTCTTGTGCCTCTACCTCCAGAATAGCTGGGATTACAGGCGTGCA T A AC018628.2,MED13 Ensembl:ENSG00000279133,Ensembl:ENSG00000108510 Other,Protein coding exon,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs936673848 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10550,RMVar_hsa_circ_85045,RMVar_hsa_circ_104817,RMVar_hsa_circ_186111,RMVar_hsa_circ_119612,RMVar_hsa_circ_81309,RMVar_hsa_circ_110787,RMVar_hsa_circ_102026,RMVar_hsa_circ_186123,RMVar_hsa_circ_186124,RMVar_hsa_circ_186122,RMVar_hsa_circ_88424,RMVar_hsa_circ_186125,RMVar_hsa_circ_186126,RMVar_hsa_circ_83249,RMVar_hsa_circ_186127,RMVar_hsa_circ_120621,RMVar_hsa_circ_186133,RMVar_hsa_circ_101240,RMVar_hsa_circ_121360,RMVar_hsa_circ_50231,RMVar_hsa_circ_186138,RMVar_hsa_circ_186139,RMVar_hsa_circ_186140,RMVar_hsa_circ_89268,RMVar_hsa_circ_186142,RMVar_hsa_circ_372759,RMVar_hsa_circ_104772,RMVar_hsa_circ_186143,RMVar_hsa_circ_186144,RMVar_hsa_circ_353824,RMVar_hsa_circ_361895,RMVar_hsa_circ_62540,RMVar_hsa_circ_123911,RMVar_hsa_circ_186152,RMVar_hsa_circ_336303,RMVar_hsa_circ_120286,RMVar_hsa_circ_186155,RMVar_hsa_circ_304263,RMVar_hsa_circ_279047,RMVar_hsa_circ_290568,RMVar_hsa_circ_355612,RMVar_hsa_circ_96938,RMVar_hsa_circ_186159,RMVar_hsa_circ_22555,RMVar_hsa_circ_298747,RMVar_hsa_circ_186158,RMVar_hsa_circ_284367,RMVar_hsa_circ_186162 40803 RMVar_ID_40803 Human_SNP_ID_629428644 A-to-I Human chr17 - 62007119 62007119 62007119 CTTCTGCCTCAGCCTCCAGAGGAACTGGGACTATAGGCACGTGCCACCACGCCTGTCTGATTTTT CTTCTGCCTCAGCCTCCAGAGGAACTGGGACTGTAGGCACGTGCCACCACGCCTGTCTGATTTTT T C AC018628.2,MED13 Ensembl:ENSG00000279133,Ensembl:ENSG00000108510 Other,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017631638 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3533254,Human_RBP_ID_6630077,Human_RBP_ID_13120511 RMVar_hsa_circ_10550,RMVar_hsa_circ_85045,RMVar_hsa_circ_104817,RMVar_hsa_circ_186111,RMVar_hsa_circ_119612,RMVar_hsa_circ_81309,RMVar_hsa_circ_110787,RMVar_hsa_circ_102026,RMVar_hsa_circ_186123,RMVar_hsa_circ_186124,RMVar_hsa_circ_186122,RMVar_hsa_circ_88424,RMVar_hsa_circ_186125,RMVar_hsa_circ_186126,RMVar_hsa_circ_83249,RMVar_hsa_circ_186127,RMVar_hsa_circ_120621,RMVar_hsa_circ_186133,RMVar_hsa_circ_101240,RMVar_hsa_circ_121360,RMVar_hsa_circ_50231,RMVar_hsa_circ_186138,RMVar_hsa_circ_186139,RMVar_hsa_circ_186140,RMVar_hsa_circ_89268,RMVar_hsa_circ_186142,RMVar_hsa_circ_372759,RMVar_hsa_circ_104772,RMVar_hsa_circ_186143,RMVar_hsa_circ_186144,RMVar_hsa_circ_353824,RMVar_hsa_circ_361895,RMVar_hsa_circ_62540,RMVar_hsa_circ_123911,RMVar_hsa_circ_186152,RMVar_hsa_circ_336303,RMVar_hsa_circ_120286,RMVar_hsa_circ_186155,RMVar_hsa_circ_304263,RMVar_hsa_circ_279047,RMVar_hsa_circ_290568,RMVar_hsa_circ_355612,RMVar_hsa_circ_96938,RMVar_hsa_circ_186159,RMVar_hsa_circ_22555,RMVar_hsa_circ_298747,RMVar_hsa_circ_186158,RMVar_hsa_circ_284367,RMVar_hsa_circ_186162 40804 RMVar_ID_40804 Human_SNP_ID_629428780 A-to-I Human chr17 - 62007592 62007592 62007592 CGCCCGCCTCGGCCTCCTAAAGTGCTGGGATTACAGGCGTGAACCACCACGCCCGGCCAAGGTCT CGCCCGCCTCGGCCTCCTAAAGTGCTGGGATTGCAGGCGTGAACCACCACGCCCGGCCAAGGTCT T C MED13 Ensembl:ENSG00000108510 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs943385511 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10550,RMVar_hsa_circ_85045,RMVar_hsa_circ_104817,RMVar_hsa_circ_186111,RMVar_hsa_circ_119612,RMVar_hsa_circ_81309,RMVar_hsa_circ_110787,RMVar_hsa_circ_102026,RMVar_hsa_circ_186123,RMVar_hsa_circ_186124,RMVar_hsa_circ_186122,RMVar_hsa_circ_88424,RMVar_hsa_circ_186125,RMVar_hsa_circ_186126,RMVar_hsa_circ_83249,RMVar_hsa_circ_186127,RMVar_hsa_circ_120621,RMVar_hsa_circ_186133,RMVar_hsa_circ_101240,RMVar_hsa_circ_121360,RMVar_hsa_circ_50231,RMVar_hsa_circ_186138,RMVar_hsa_circ_186139,RMVar_hsa_circ_186140,RMVar_hsa_circ_89268,RMVar_hsa_circ_186142,RMVar_hsa_circ_372759,RMVar_hsa_circ_104772,RMVar_hsa_circ_186143,RMVar_hsa_circ_186144,RMVar_hsa_circ_353824,RMVar_hsa_circ_361895,RMVar_hsa_circ_62540,RMVar_hsa_circ_123911,RMVar_hsa_circ_186152,RMVar_hsa_circ_336303,RMVar_hsa_circ_120286,RMVar_hsa_circ_186155,RMVar_hsa_circ_304263,RMVar_hsa_circ_279047,RMVar_hsa_circ_290568,RMVar_hsa_circ_355612,RMVar_hsa_circ_96938,RMVar_hsa_circ_186159,RMVar_hsa_circ_22555,RMVar_hsa_circ_298747,RMVar_hsa_circ_186158,RMVar_hsa_circ_284367,RMVar_hsa_circ_186162 40805 RMVar_ID_40805 Human_SNP_ID_629430508 A-to-I Human chr17 - 62012921 62012921 62012921 AGGTGTGGTGGTGCACGCCTGTAGTTCCAGCTACTTGGGAGGCTGAGGCAGGAAAACTGCTTGAA AGGTGTGGTGGTGCACGCCTGTAGTTCCAGCTGCTTGGGAGGCTGAGGCAGGAAAACTGCTTGAA T C MED13 Ensembl:ENSG00000108510 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs759433887 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10550,RMVar_hsa_circ_85045,RMVar_hsa_circ_104817,RMVar_hsa_circ_186111,RMVar_hsa_circ_119612,RMVar_hsa_circ_81309,RMVar_hsa_circ_110787,RMVar_hsa_circ_102026,RMVar_hsa_circ_186123,RMVar_hsa_circ_186124,RMVar_hsa_circ_186122,RMVar_hsa_circ_88424,RMVar_hsa_circ_186125,RMVar_hsa_circ_186126,RMVar_hsa_circ_83249,RMVar_hsa_circ_186127,RMVar_hsa_circ_120621,RMVar_hsa_circ_186133,RMVar_hsa_circ_101240,RMVar_hsa_circ_121360,RMVar_hsa_circ_50231,RMVar_hsa_circ_186138,RMVar_hsa_circ_186139,RMVar_hsa_circ_186140,RMVar_hsa_circ_89268,RMVar_hsa_circ_186142,RMVar_hsa_circ_372759,RMVar_hsa_circ_186143,RMVar_hsa_circ_361895,RMVar_hsa_circ_62540,RMVar_hsa_circ_123911,RMVar_hsa_circ_186152,RMVar_hsa_circ_336303,RMVar_hsa_circ_120286,RMVar_hsa_circ_186155,RMVar_hsa_circ_279047,RMVar_hsa_circ_355612,RMVar_hsa_circ_96938,RMVar_hsa_circ_22555,RMVar_hsa_circ_186158,RMVar_hsa_circ_284367,RMVar_hsa_circ_284175,RMVar_hsa_circ_329803,RMVar_hsa_circ_365948,RMVar_hsa_circ_320136,RMVar_hsa_circ_325286,RMVar_hsa_circ_291257,RMVar_hsa_circ_186166,RMVar_hsa_circ_186165 40806 RMVar_ID_40806 Human_SNP_ID_629433611 A-to-I Human chr17 - 62021910 62021910 62021910 CACGTACCTTGGCCTCCCAAAGTGCAGGAATTACAGACGTGAGCCACTGTGCCCAGGCTTTAGAA CACGTACCTTGGCCTCCCAAAGTGCAGGAATTGCAGACGTGAGCCACTGTGCCCAGGCTTTAGAA T C MED13 Ensembl:ENSG00000108510 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1033140595 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10550,RMVar_hsa_circ_85045,RMVar_hsa_circ_104817,RMVar_hsa_circ_186111,RMVar_hsa_circ_119612,RMVar_hsa_circ_81309,RMVar_hsa_circ_110787,RMVar_hsa_circ_102026,RMVar_hsa_circ_186123,RMVar_hsa_circ_186124,RMVar_hsa_circ_186122,RMVar_hsa_circ_88424,RMVar_hsa_circ_186125,RMVar_hsa_circ_186126,RMVar_hsa_circ_83249,RMVar_hsa_circ_186127,RMVar_hsa_circ_120621,RMVar_hsa_circ_186133,RMVar_hsa_circ_101240,RMVar_hsa_circ_121360,RMVar_hsa_circ_50231,RMVar_hsa_circ_186138,RMVar_hsa_circ_186139,RMVar_hsa_circ_186140,RMVar_hsa_circ_89268,RMVar_hsa_circ_186142,RMVar_hsa_circ_372759,RMVar_hsa_circ_186143,RMVar_hsa_circ_361895,RMVar_hsa_circ_62540,RMVar_hsa_circ_123911,RMVar_hsa_circ_186152,RMVar_hsa_circ_336303,RMVar_hsa_circ_120286,RMVar_hsa_circ_186155,RMVar_hsa_circ_279047,RMVar_hsa_circ_355612,RMVar_hsa_circ_96938,RMVar_hsa_circ_22555,RMVar_hsa_circ_186158,RMVar_hsa_circ_284367,RMVar_hsa_circ_284175,RMVar_hsa_circ_329803,RMVar_hsa_circ_365948,RMVar_hsa_circ_320136,RMVar_hsa_circ_325286,RMVar_hsa_circ_291257,RMVar_hsa_circ_186166,RMVar_hsa_circ_186165 40807 RMVar_ID_40807 Human_SNP_ID_629433654 A-to-I Human chr17 - 62022046 62022046 62022046 CTTGTGCCTCAGCCTCCTGAGTAGCTGGTGCTACAGGTATATACCACCACATCCAGATTAATTGT CTTGTGCCTCAGCCTCCTGAGTAGCTGGTGCTGCAGGTATATACCACCACATCCAGATTAATTGT T C MED13 Ensembl:ENSG00000108510 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1301998343 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10550,RMVar_hsa_circ_85045,RMVar_hsa_circ_104817,RMVar_hsa_circ_186111,RMVar_hsa_circ_119612,RMVar_hsa_circ_81309,RMVar_hsa_circ_110787,RMVar_hsa_circ_102026,RMVar_hsa_circ_186123,RMVar_hsa_circ_186124,RMVar_hsa_circ_186122,RMVar_hsa_circ_88424,RMVar_hsa_circ_186125,RMVar_hsa_circ_186126,RMVar_hsa_circ_83249,RMVar_hsa_circ_186127,RMVar_hsa_circ_120621,RMVar_hsa_circ_186133,RMVar_hsa_circ_101240,RMVar_hsa_circ_121360,RMVar_hsa_circ_50231,RMVar_hsa_circ_186138,RMVar_hsa_circ_186139,RMVar_hsa_circ_186140,RMVar_hsa_circ_89268,RMVar_hsa_circ_186142,RMVar_hsa_circ_372759,RMVar_hsa_circ_186143,RMVar_hsa_circ_361895,RMVar_hsa_circ_62540,RMVar_hsa_circ_123911,RMVar_hsa_circ_186152,RMVar_hsa_circ_336303,RMVar_hsa_circ_120286,RMVar_hsa_circ_186155,RMVar_hsa_circ_279047,RMVar_hsa_circ_355612,RMVar_hsa_circ_96938,RMVar_hsa_circ_22555,RMVar_hsa_circ_186158,RMVar_hsa_circ_284367,RMVar_hsa_circ_284175,RMVar_hsa_circ_329803,RMVar_hsa_circ_365948,RMVar_hsa_circ_320136,RMVar_hsa_circ_325286,RMVar_hsa_circ_291257,RMVar_hsa_circ_186166,RMVar_hsa_circ_186165 40808 RMVar_ID_40808 Human_SNP_ID_629435475 A-to-I Human chr17 - 62029145 62029145 62029145 GAGTTCTTTCTTTTTTTAAAAAATGAAGAGACAGGGTCTTGCTTTGTTACCCAGGCTGGAGTGAT GAGTTCTTTCTTTTTTTAAAAAATGAAGAGACGGGGTCTTGCTTTGTTACCCAGGCTGGAGTGAT T C MED13 Ensembl:ENSG00000108510 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1203977598 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10550,RMVar_hsa_circ_85045,RMVar_hsa_circ_104817,RMVar_hsa_circ_186111,RMVar_hsa_circ_119612,RMVar_hsa_circ_81309,RMVar_hsa_circ_110787,RMVar_hsa_circ_102026,RMVar_hsa_circ_186123,RMVar_hsa_circ_186124,RMVar_hsa_circ_186122,RMVar_hsa_circ_88424,RMVar_hsa_circ_186125,RMVar_hsa_circ_186126,RMVar_hsa_circ_83249,RMVar_hsa_circ_186127,RMVar_hsa_circ_120621,RMVar_hsa_circ_186133,RMVar_hsa_circ_101240,RMVar_hsa_circ_121360,RMVar_hsa_circ_50231,RMVar_hsa_circ_186138,RMVar_hsa_circ_186139,RMVar_hsa_circ_186140,RMVar_hsa_circ_89268,RMVar_hsa_circ_186142,RMVar_hsa_circ_372759,RMVar_hsa_circ_186143,RMVar_hsa_circ_361895,RMVar_hsa_circ_62540,RMVar_hsa_circ_123911,RMVar_hsa_circ_186152,RMVar_hsa_circ_336303,RMVar_hsa_circ_120286,RMVar_hsa_circ_186155,RMVar_hsa_circ_279047,RMVar_hsa_circ_355612,RMVar_hsa_circ_96938,RMVar_hsa_circ_22555,RMVar_hsa_circ_186158,RMVar_hsa_circ_284367,RMVar_hsa_circ_284175,RMVar_hsa_circ_329803,RMVar_hsa_circ_365948,RMVar_hsa_circ_320136,RMVar_hsa_circ_325286,RMVar_hsa_circ_291257,RMVar_hsa_circ_186166,RMVar_hsa_circ_186165 40809 RMVar_ID_40809 Human_SNP_ID_629437642 A-to-I Human chr17 - 62037072 62037072 62037072 ATTTTTTGTATTTTTAGGGAGATGGAGGTTTCACCATGTTGGCCATGCTGGTCTTGAACTCTTGG ATTTTTTGTATTTTTAGGGAGATGGAGGTTTCGCCATGTTGGCCATGCTGGTCTTGAACTCTTGG T C MED13 Ensembl:ENSG00000108510 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1203362202 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25314146 RMVar_hsa_circ_81309,RMVar_hsa_circ_186124,RMVar_hsa_circ_62540,RMVar_hsa_circ_320136,RMVar_hsa_circ_291257,RMVar_hsa_circ_279052,RMVar_hsa_circ_314123,RMVar_hsa_circ_186173,RMVar_hsa_circ_186172,RMVar_hsa_circ_103824,RMVar_hsa_circ_371725,RMVar_hsa_circ_23257,RMVar_hsa_circ_186175,RMVar_hsa_circ_186174,RMVar_hsa_circ_85038,RMVar_hsa_circ_186179,RMVar_hsa_circ_81214,RMVar_hsa_circ_186181 40810 RMVar_ID_40810 Human_SNP_ID_629437846 A-to-I Human chr17 - 62037786 62037786 62037786 CACACCCAGCTAATTTTTGTATTTTTAGTAGAAACAGAATTTCACCTTGTTGGCCAGGCTGGTCT CACACCCAGCTAATTTTTGTATTTTTAGTAGAGACAGAATTTCACCTTGTTGGCCAGGCTGGTCT T C MED13 Ensembl:ENSG00000108510 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1465332745 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13121359 RMVar_hsa_circ_81309,RMVar_hsa_circ_186124,RMVar_hsa_circ_62540,RMVar_hsa_circ_320136,RMVar_hsa_circ_291257,RMVar_hsa_circ_279052,RMVar_hsa_circ_314123,RMVar_hsa_circ_186173,RMVar_hsa_circ_186172,RMVar_hsa_circ_103824,RMVar_hsa_circ_371725,RMVar_hsa_circ_23257,RMVar_hsa_circ_186175,RMVar_hsa_circ_186174,RMVar_hsa_circ_85038,RMVar_hsa_circ_186179,RMVar_hsa_circ_81214,RMVar_hsa_circ_186181 40811 RMVar_ID_40811 Human_SNP_ID_629438921 A-to-I Human chr17 - 62041732 62041732 62041732 CAAAAAATAAATTCTAAAAATTATCTGGACATAGTGGCTCACACCTGTAGTCCCACCTAACTTCG CAAAAAATAAATTCTAAAAATTATCTGGACATCGTGGCTCACACCTGTAGTCCCACCTAACTTCG T G MED13 Ensembl:ENSG00000108510 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs902069507 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13121494 RMVar_hsa_circ_81309,RMVar_hsa_circ_186124,RMVar_hsa_circ_62540,RMVar_hsa_circ_320136,RMVar_hsa_circ_291257,RMVar_hsa_circ_279052,RMVar_hsa_circ_314123,RMVar_hsa_circ_186173,RMVar_hsa_circ_186172,RMVar_hsa_circ_103824,RMVar_hsa_circ_371725,RMVar_hsa_circ_23257,RMVar_hsa_circ_186175,RMVar_hsa_circ_186174,RMVar_hsa_circ_85038,RMVar_hsa_circ_186179,RMVar_hsa_circ_81214,RMVar_hsa_circ_186181 40812 RMVar_ID_40812 Human_SNP_ID_629439239 A-to-I Human chr17 - 62042928 62042928 62042928 CCAGGCTGGTCTCTAACTCCTAGCCTCAAGTGATCCTCCAGCCTCAGCCTCTCAAAGTACTGGGA CCAGGCTGGTCTCTAACTCCTAGCCTCAAGTGGTCCTCCAGCCTCAGCCTCTCAAAGTACTGGGA T C MED13 Ensembl:ENSG00000108510 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1468050398 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13121534 RMVar_hsa_circ_81309,RMVar_hsa_circ_186124,RMVar_hsa_circ_62540,RMVar_hsa_circ_320136,RMVar_hsa_circ_291257,RMVar_hsa_circ_279052,RMVar_hsa_circ_314123,RMVar_hsa_circ_186173,RMVar_hsa_circ_186172,RMVar_hsa_circ_103824,RMVar_hsa_circ_371725,RMVar_hsa_circ_23257,RMVar_hsa_circ_186175,RMVar_hsa_circ_186174,RMVar_hsa_circ_85038,RMVar_hsa_circ_186179,RMVar_hsa_circ_81214,RMVar_hsa_circ_186181 40813 RMVar_ID_40813 Human_SNP_ID_629440258 A-to-I Human chr17 - 62046654 62046654 62046654 TTTTGTAGATTTTGTAGAGACAAGATATCACCATGTTGCCTAGGCTGGTCTTGAACTGAGCTCAA TTTTGTAGATTTTGTAGAGACAAGATATCACCGTGTTGCCTAGGCTGGTCTTGAACTGAGCTCAA T C MED13 Ensembl:ENSG00000108510 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1162348784 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13121703,Human_RBP_ID_25314272 RMVar_hsa_circ_81309,RMVar_hsa_circ_186124,RMVar_hsa_circ_62540,RMVar_hsa_circ_320136,RMVar_hsa_circ_291257,RMVar_hsa_circ_279052,RMVar_hsa_circ_314123,RMVar_hsa_circ_186173,RMVar_hsa_circ_186172,RMVar_hsa_circ_103824,RMVar_hsa_circ_371725,RMVar_hsa_circ_23257,RMVar_hsa_circ_186175,RMVar_hsa_circ_186174,RMVar_hsa_circ_85038,RMVar_hsa_circ_186179,RMVar_hsa_circ_81214,RMVar_hsa_circ_186181 40814 RMVar_ID_40814 Human_SNP_ID_629440278 A-to-I Human chr17 - 62046755 62046755 62046755 CATGGCTCATTGCAGCCCAAACTGCCAGGCTCAAGTAGTCCTCACACCTCAGCCTCCCATGTAGC CATGGCTCATTGCAGCCCAAACTGCCAGGCTCGAGTAGTCCTCACACCTCAGCCTCCCATGTAGC T C MED13 Ensembl:ENSG00000108510 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982144215 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17566965 RMVar_hsa_circ_81309,RMVar_hsa_circ_186124,RMVar_hsa_circ_62540,RMVar_hsa_circ_320136,RMVar_hsa_circ_291257,RMVar_hsa_circ_279052,RMVar_hsa_circ_314123,RMVar_hsa_circ_186173,RMVar_hsa_circ_186172,RMVar_hsa_circ_103824,RMVar_hsa_circ_371725,RMVar_hsa_circ_23257,RMVar_hsa_circ_186175,RMVar_hsa_circ_186174,RMVar_hsa_circ_85038,RMVar_hsa_circ_186179,RMVar_hsa_circ_81214,RMVar_hsa_circ_186181 40815 RMVar_ID_40815 Human_SNP_ID_629440470 A-to-I Human chr17 - 62047352 62047352 62047352 TTCTTTTTGTTTTTGAGATGAAGTCTTGCTCTATCGCCCAGGGTGGAGTACAGTGGCATGATTTC TTCTTTTTGTTTTTGAGATGAAGTCTTGCTCTGTCGCCCAGGGTGGAGTACAGTGGCATGATTTC T C MED13 Ensembl:ENSG00000108510 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs867933804 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13121727 RMVar_hsa_circ_81309,RMVar_hsa_circ_186124,RMVar_hsa_circ_62540,RMVar_hsa_circ_320136,RMVar_hsa_circ_291257,RMVar_hsa_circ_279052,RMVar_hsa_circ_314123,RMVar_hsa_circ_186173,RMVar_hsa_circ_186172,RMVar_hsa_circ_103824,RMVar_hsa_circ_371725,RMVar_hsa_circ_23257,RMVar_hsa_circ_186175,RMVar_hsa_circ_186174,RMVar_hsa_circ_85038,RMVar_hsa_circ_186179,RMVar_hsa_circ_81214,RMVar_hsa_circ_186181 40816 RMVar_ID_40816 Human_SNP_ID_629535337 A-to-I Human chr17 + 62431139 62431139 62431139 CACCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACTGCACCCAGCTAATTTTT CACCCGCCTCAGCCTCCCAAAGTGCTGGGATTCCAGGTGTGAGCCACTGCACCCAGCTAATTTTT A C METTL2A Ensembl:ENSG00000087995 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs988811790 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_186182,RMVar_hsa_circ_371335,RMVar_hsa_circ_361482 40817 RMVar_ID_40817 Human_SNP_ID_629537966 A-to-I Human chr17 + 62442513 62442513 62442513 GTTGGCCAGGCTGGTCTTGAACTCCTTACCTCAAGTTATCCACCCACCTCGGCATCCCAAAGTGC GTTGGCCAGGCTGGTCTTGAACTCCTTACCTCGAGTTATCCACCCACCTCGGCATCCCAAAGTGC A G METTL2A Ensembl:ENSG00000087995 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1281650883 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25050,RMVar_hsa_circ_186182,RMVar_hsa_circ_371335,RMVar_hsa_circ_126933,RMVar_hsa_circ_186184,RMVar_hsa_circ_102930,RMVar_hsa_circ_186183,RMVar_hsa_circ_280537,RMVar_hsa_circ_186185 40818 RMVar_ID_40818 Human_SNP_ID_629539472 A-to-I Human chr17 + 62448821 62448821 62448821 AAATTGTAGCACTGGGCGTGGTGCATGCCTGTAATCCCAGCCACTCAGGAGGCTGAGGCGGGGAG AAATTGTAGCACTGGGCGTGGTGCATGCCTGTGATCCCAGCCACTCAGGAGGCTGAGGCGGGGAG A G METTL2A Ensembl:ENSG00000087995 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1402590311 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_496696,Human_RBP_ID_1539655,Human_RBP_ID_5114806,Human_RBP_ID_17653692 40819 RMVar_ID_40819 Human_SNP_ID_629539631 A-to-I Human chr17 + 62449501 62449501 62449501 GGGAGGCCAAGGCGGGCGGATCAGCTGAGGTCAGGAGTTGGAGACCAGCGTGGCCAACATGGTGA GGGAGGCCAAGGCGGGCGGATCAGCTGAGGTCCGGAGTTGGAGACCAGCGTGGCCAACATGGTGA A C METTL2A Ensembl:ENSG00000087995 Protein coding 3'UTR GSE38233;GSE99789;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;esophageal squamous carcinoma cells,EC109;ASD brains,temporal_cortex;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29796672,30559470,31158229,31158229 RNA-Seq:(High) rs1203321468 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13122576 40820 RMVar_ID_40820 Human_SNP_ID_629539632 A-to-I Human chr17 + 62449501 62449501 62449501 GGGAGGCCAAGGCGGGCGGATCAGCTGAGGTCAGGAGTTGGAGACCAGCGTGGCCAACATGGTGA GGGAGGCCAAGGCGGGCGGATCAGCTGAGGTCGGGAGTTGGAGACCAGCGTGGCCAACATGGTGA A G METTL2A Ensembl:ENSG00000087995 Protein coding 3'UTR GSE38233;GSE99789;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;esophageal squamous carcinoma cells,EC109;ASD brains,temporal_cortex;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29796672,30559470,31158229,31158229 RNA-Seq:(High) rs1203321468 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13122576 40821 RMVar_ID_40821 Human_SNP_ID_629539669 A-to-I Human chr17 + 62449651 62449651 62449651 AGAATTGCTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCTGAGATTGTGCCACTGCACTCCAGCC AGAATTGCTTGAACCCAGGAGGCAGAGGTTGCCGTGAGCTGAGATTGTGCCACTGCACTCCAGCC A C METTL2A Ensembl:ENSG00000087995 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs983779753 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_619859 40822 RMVar_ID_40822 Human_SNP_ID_629539751 A-to-I Human chr17 + 62449983 62449983 62449983 GCACACACCTGTAGTCCCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGTTTGAA GCACACACCTGTAGTCCCCTGTAGTCCCAGCTTCTCGGGAGGCTGAGGCAGGAGAATCGTTTGAA A T METTL2A Ensembl:ENSG00000087995 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1364863578 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13122577,Human_RBP_ID_18705458 40823 RMVar_ID_40823 Human_SNP_ID_629539875 A-to-I Human chr17 + 62450285 62450284 62450286 TTTTTTTTTTTTTTTTTTTTTTTTAAGGAGACAGGGCTCTCACTTTGTTGCCCAGGCTGGAGTTC TTTTTTTTTTTTTTTTTTTTTTTTAAGGAGAC__GGCTCTCACTTTGTTGCCCAGGCTGGAGTTC CAG C METTL2A Ensembl:ENSG00000087995 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs143399803 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_8191359,Human_RBP_ID_26459658 40824 RMVar_ID_40824 Human_SNP_ID_629539887 A-to-I Human chr17 + 62450361 62450361 62450361 GATAGCTCATTATCACCTCAAACTTCTGGCTCAAGCCATCCCTCCGCCTCAGCCTCCTGAGTAGC GATAGCTCATTATCACCTCAAACTTCTGGCTCGAGCCATCCCTCCGCCTCAGCCTCCTGAGTAGC A G METTL2A Ensembl:ENSG00000087995 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs955633853 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13122583,Human_RBP_ID_26454219 40825 RMVar_ID_40825 Human_SNP_ID_629539941 A-to-I Human chr17 + 62450567 62450567 62450567 GACTTTTCGACCAGGCGTGGCGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCCGAGGTGGGC GACTTTTCGACCAGGCGTGGCGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGC A G METTL2A Ensembl:ENSG00000087995 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs112610403 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_496702,Human_RBP_ID_26459662 40826 RMVar_ID_40826 Human_SNP_ID_629540073 A-to-I Human chr17 + 62451165 62451165 62451165 AAGACCCTGACTTTTTTTTTTTTTTTTTTTTGAGACAGAGCTTCGCTCTTGTTGCCCAGGCTGGA AAGACCCTGACTTTTTTTTTTTTTTTTTTTTGTGACAGAGCTTCGCTCTTGTTGCCCAGGCTGGA A T METTL2A Ensembl:ENSG00000087995 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1181590362 Functional Loss SNV dbSNP153 33..33 33 - - - 40827 RMVar_ID_40827 Human_SNP_ID_629540169 A-to-I Human chr17 + 62451501 62451501 62451501 ATGTTAAAAATAGGCCGGGTGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGT ATGTTAAAAATAGGCCGGGTGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGT A G METTL2A Ensembl:ENSG00000087995 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs568215485 Functional Loss SNV dbSNP153 33..33 33 - - - 40828 RMVar_ID_40828 Human_SNP_ID_629540170 A-to-I Human chr17 + 62451501 62451501 62451501 ATGTTAAAAATAGGCCGGGTGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGT ATGTTAAAAATAGGCCGGGTGCGGTGGCTCACTCCTGTAATCCCAGCACTTTGGGAGGCCAAGGT A T METTL2A Ensembl:ENSG00000087995 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs568215485 Functional Loss SNV dbSNP153 33..33 33 - - - 40829 RMVar_ID_40829 Human_SNP_ID_629540192 A-to-I Human chr17 + 62451592 62451592 62451592 CGAGACCAGCCTGGCCAACTTAATGAAACCCCATCACTGCTAACAATACAGACCTGGCACGGTGG CGAGACCAGCCTGGCCAACTTAATGAAACCCCCTCACTGCTAACAATACAGACCTGGCACGGTGG A C METTL2A Ensembl:ENSG00000087995 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs566735481 Functional Loss SNV dbSNP153 33..33 33 - - - 40830 RMVar_ID_40830 Human_SNP_ID_629540250 A-to-I Human chr17 + 62451831 62451831 62451831 AGAATCACTTGAATCTGGGAGGCGGAGGTTGCAGTGAGCCGAGATGGCACCATTGCACTCCAGCC AGAATCACTTGAATCTGGGAGGCGGAGGTTGCGGTGAGCCGAGATGGCACCATTGCACTCCAGCC A G METTL2A Ensembl:ENSG00000087995 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1376643581 Functional Loss SNV dbSNP153 33..33 33 - - - 40831 RMVar_ID_40831 Human_SNP_ID_629546175 A-to-I Human chr17 - 62475027 62475027 62475027 TTTTGTTGTTGTTTGAGACAAAGTTTGGCTCTATCGCCCAGGATGGAGTGCAATGGCACAATCTC TTTTGTTGTTGTTTGAGACAAAGTTTGGCTCTGTCGCCCAGGATGGAGTGCAATGGCACAATCTC T C lnc-MARCH10-8,lnc-MARCH10-8:2,lnc-MARCH10-8:3,lnc-MARCH10-8:4,lnc-MARCH10-8:5,lnc-MARCH10-8:6 RNACentral:URS0000D579EF,RNACentral:URS0000D58451,RNACentral:URS0000D59CE0,RNACentral:URS0000D5ACE5,RNACentral:URS0000D573AB,RNACentral:URS0000D56EFF lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,intron,exon,exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs535761743 Functional Loss SNV dbSNP153 33..33 33 - - - 40832 RMVar_ID_40832 Human_SNP_ID_629546296 A-to-I Human chr17 - 62475475 62475475 62475475 AGCTGAGCGTGGTGGTGGGCACCTGTAATCCCAGCTAGTCGGGAGACTGAGGCAGGAGAATCGCT AGCTGAGCGTGGTGGTGGGCACCTGTAATCCCTGCTAGTCGGGAGACTGAGGCAGGAGAATCGCT T A lnc-MARCH10-8,lnc-MARCH10-8:2,lnc-MARCH10-8:3,lnc-MARCH10-8:4,lnc-MARCH10-8:5,lnc-MARCH10-8:6 RNACentral:URS0000D579EF,RNACentral:URS0000D58451,RNACentral:URS0000D59CE0,RNACentral:URS0000D5ACE5,RNACentral:URS0000D573AB,RNACentral:URS0000D56EFF lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,intron,exon,exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs778388015 Functional Loss SNV dbSNP153 33..33 33 - - - 40833 RMVar_ID_40833 Human_SNP_ID_629546297 A-to-I Human chr17 - 62475475 62475475 62475475 AGCTGAGCGTGGTGGTGGGCACCTGTAATCCCAGCTAGTCGGGAGACTGAGGCAGGAGAATCGCT AGCTGAGCGTGGTGGTGGGCACCTGTAATCCCGGCTAGTCGGGAGACTGAGGCAGGAGAATCGCT T C lnc-MARCH10-8,lnc-MARCH10-8:2,lnc-MARCH10-8:3,lnc-MARCH10-8:4,lnc-MARCH10-8:5,lnc-MARCH10-8:6 RNACentral:URS0000D579EF,RNACentral:URS0000D58451,RNACentral:URS0000D59CE0,RNACentral:URS0000D5ACE5,RNACentral:URS0000D573AB,RNACentral:URS0000D56EFF lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,intron,exon,exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs778388015 Functional Loss SNV dbSNP153 33..33 33 - - - 40834 RMVar_ID_40834 Human_SNP_ID_629546298 A-to-I Human chr17 - 62475480 62475480 62475480 AAATTAGCTGAGCGTGGTGGTGGGCACCTGTAATCCCAGCTAGTCGGGAGACTGAGGCAGGAGAA AAATTAGCTGAGCGTGGTGGTGGGCACCTGTAGTCCCAGCTAGTCGGGAGACTGAGGCAGGAGAA T C lnc-MARCH10-8,lnc-MARCH10-8:2,lnc-MARCH10-8:3,lnc-MARCH10-8:4,lnc-MARCH10-8:5,lnc-MARCH10-8:6 RNACentral:URS0000D579EF,RNACentral:URS0000D58451,RNACentral:URS0000D59CE0,RNACentral:URS0000D5ACE5,RNACentral:URS0000D573AB,RNACentral:URS0000D56EFF lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,intron,exon,exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1413119208 Functional Loss SNV dbSNP153 33..33 33 - - - 40835 RMVar_ID_40835 Human_SNP_ID_629546299 A-to-I Human chr17 - 62475487 62475487 62475487 ATTTTTTAAATTAGCTGAGCGTGGTGGTGGGCACCTGTAATCCCAGCTAGTCGGGAGACTGAGGC ATTTTTTAAATTAGCTGAGCGTGGTGGTGGGCGCCTGTAATCCCAGCTAGTCGGGAGACTGAGGC T C lnc-MARCH10-8,lnc-MARCH10-8:2,lnc-MARCH10-8:3,lnc-MARCH10-8:4,lnc-MARCH10-8:5,lnc-MARCH10-8:6 RNACentral:URS0000D579EF,RNACentral:URS0000D58451,RNACentral:URS0000D59CE0,RNACentral:URS0000D5ACE5,RNACentral:URS0000D573AB,RNACentral:URS0000D56EFF lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,intron,exon,exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1466358028 Functional Loss SNV dbSNP153 33..33 33 - - - 40836 RMVar_ID_40836 Human_SNP_ID_629546504 A-to-I Human chr17 - 62476091 62476091 62476091 CCTGTACTTTCAGCTACTTGGGAGGTTGAGACAGGAGAATTTTGCTTGAACCCAGGAGGCGGAGG CCTGTACTTTCAGCTACTTGGGAGGTTGAGACGGGAGAATTTTGCTTGAACCCAGGAGGCGGAGG T C lnc-MARCH10-8,lnc-MARCH10-8:2,lnc-MARCH10-8:3,lnc-MARCH10-8:4,lnc-MARCH10-8:5,lnc-MARCH10-8:6 RNACentral:URS0000D579EF,RNACentral:URS0000D58451,RNACentral:URS0000D59CE0,RNACentral:URS0000D5ACE5,RNACentral:URS0000D573AB,RNACentral:URS0000D56EFF lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,intron,exon,exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs537330129 Functional Loss SNV dbSNP153 33..33 33 - - - 40837 RMVar_ID_40837 Human_SNP_ID_629546646 A-to-I Human chr17 - 62476501 62476501 62476501 TCAGCTTGCTGCAACCTCTTTCTCCTGGGTTCATGCGATTCTCCCGCCTCAGCCTCCCAACTAGC TCAGCTTGCTGCAACCTCTTTCTCCTGGGTTCGTGCGATTCTCCCGCCTCAGCCTCCCAACTAGC T C lnc-MARCH10-8,lnc-MARCH10-8:2,lnc-MARCH10-8:3,lnc-MARCH10-8:4,lnc-MARCH10-8:5,lnc-MARCH10-8:6 RNACentral:URS0000D579EF,RNACentral:URS0000D58451,RNACentral:URS0000D59CE0,RNACentral:URS0000D5ACE5,RNACentral:URS0000D573AB,RNACentral:URS0000D56EFF lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,intron,exon,exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417919140 Functional Loss SNV dbSNP153 33..33 33 - - - 40838 RMVar_ID_40838 Human_SNP_ID_629546647 A-to-I Human chr17 - 62476501 62476501 62476501 TCAGCTTGCTGCAACCTCTTTCTCCTGGGTTCATGCGATTCTCCCGCCTCAGCCTCCCAACTAGC TCAGCTTGCTGCAACCTCTTTCTCCTGGGTTCCTGCGATTCTCCCGCCTCAGCCTCCCAACTAGC T G lnc-MARCH10-8,lnc-MARCH10-8:2,lnc-MARCH10-8:3,lnc-MARCH10-8:4,lnc-MARCH10-8:5,lnc-MARCH10-8:6 RNACentral:URS0000D579EF,RNACentral:URS0000D58451,RNACentral:URS0000D59CE0,RNACentral:URS0000D5ACE5,RNACentral:URS0000D573AB,RNACentral:URS0000D56EFF lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,intron,exon,exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417919140 Functional Loss SNV dbSNP153 33..33 33 - - - 40839 RMVar_ID_40839 Human_SNP_ID_629546665 A-to-I Human chr17 - 62476577 62476577 62476577 TATTTTATTTTATTTTATTTTATTTTGGTGACAGAGTCTCACACTGTCGCCCGGGCTGAAGTGCA TATTTTATTTTATTTTATTTTATTTTGGTGACGGAGTCTCACACTGTCGCCCGGGCTGAAGTGCA T C lnc-MARCH10-8,lnc-MARCH10-8:2,lnc-MARCH10-8:3,lnc-MARCH10-8:4,lnc-MARCH10-8:5,lnc-MARCH10-8:6 RNACentral:URS0000D579EF,RNACentral:URS0000D58451,RNACentral:URS0000D59CE0,RNACentral:URS0000D5ACE5,RNACentral:URS0000D573AB,RNACentral:URS0000D56EFF lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,intron,exon,exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1481198454 Functional Loss SNV dbSNP153 33..33 33 - - - 40840 RMVar_ID_40840 Human_SNP_ID_629555127 A-to-I Human chr17 + 62509272 62509271 62509273 CACCACACCCGGGTAATTTTCTAATTTTTTGTAGAGATGGGATCTTGCTATGCTGCCCAAGCTGG CACCACACCCGGGTAATTTTCTAATTTTTTGT__AGATGGGATCTTGCTATGCTGCCCAAGCTGG TAG T TLK2 Ensembl:ENSG00000146872 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1361634917 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_101174,RMVar_hsa_circ_104743,RMVar_hsa_circ_121410,RMVar_hsa_circ_186187,RMVar_hsa_circ_120325,RMVar_hsa_circ_186188,RMVar_hsa_circ_339231,RMVar_hsa_circ_31561,RMVar_hsa_circ_186189,RMVar_hsa_circ_186190,RMVar_hsa_circ_57369 40841 RMVar_ID_40841 Human_SNP_ID_629574414 A-to-I Human chr17 + 62591128 62591128 62591128 AAAATTAGCTGGGCATGGTGGCACGCACCTGTAATCCCACCTACTTGGGAGGCTGAGGCAGAAGA AAAATTAGCTGGGCATGGTGGCACGCACCTGTGATCCCACCTACTTGGGAGGCTGAGGCAGAAGA A G TLK2 Ensembl:ENSG00000146872 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs921667255 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1739,RMVar_hsa_circ_123972,RMVar_hsa_circ_186197,RMVar_hsa_circ_105826,RMVar_hsa_circ_186202,RMVar_hsa_circ_34993,RMVar_hsa_circ_23423,RMVar_hsa_circ_9745,RMVar_hsa_circ_108797,RMVar_hsa_circ_110896,RMVar_hsa_circ_186220,RMVar_hsa_circ_186219,RMVar_hsa_circ_186227,RMVar_hsa_circ_15300,RMVar_hsa_circ_108597,RMVar_hsa_circ_186224,RMVar_hsa_circ_362286,RMVar_hsa_circ_15062,RMVar_hsa_circ_316047,RMVar_hsa_circ_325245,RMVar_hsa_circ_337750,RMVar_hsa_circ_272557,RMVar_hsa_circ_186228,RMVar_hsa_circ_186226 40842 RMVar_ID_40842 Human_SNP_ID_629577927 A-to-I Human chr17 + 62605573 62605573 62605573 TTTTGTATTTTTAGTAGAGATAGGGTTTCGCCATGTTGCCCAGGCTGGTCTCAAATTCTTGAGTT TTTTGTATTTTTAGTAGAGATAGGGTTTCGCCGTGTTGCCCAGGCTGGTCTCAAATTCTTGAGTT A G TLK2 Ensembl:ENSG00000146872 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1240726024 Functional Loss SNV dbSNP153 33..33 33 - - - 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 40843 RMVar_ID_40843 Human_SNP_ID_629577965 A-to-I Human chr17 + 62605785 62605785 62605785 CCAGTACTTTAGGAGGTCGAGCTGGGAGGATCACTTGAGTCCAGGAGTTTGAGACCAGCCTGGGC CCAGTACTTTAGGAGGTCGAGCTGGGAGGATCCCTTGAGTCCAGGAGTTTGAGACCAGCCTGGGC A C TLK2 Ensembl:ENSG00000146872 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1258796093 Functional Loss SNV dbSNP153 33..33 33 - - - 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 40844 RMVar_ID_40844 Human_SNP_ID_629585977 A-to-I Human chr17 + 62637481 62637481 62637481 TCACTTGAACCCTGGAGGTGGAGGTTGCAGTGAGCTGAGATCACGCCATTGCACTCCAGCCTGGG TCACTTGAACCCTGGAGGTGGAGGTTGCAGTGCGCTGAGATCACGCCATTGCACTCCAGCCTGGG A C MRC2 Ensembl:ENSG00000011028 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1181034216 Functional Loss SNV dbSNP153 33..33 33 - - - 40845 RMVar_ID_40845 Human_SNP_ID_629628624 A-to-I Human chr17 + 62805702 62805702 62805702 CAGAGGCCAAGGCAGGTGGATCACTTGAGGTCAGGAGTTCGAGATCGGCCTGGCCAACGTGGCAA CAGAGGCCAAGGCAGGTGGATCACTTGAGGTCGGGAGTTCGAGATCGGCCTGGCCAACGTGGCAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs564140114 Functional Loss SNV dbSNP153 33..33 33 - - - 40846 RMVar_ID_40846 Human_SNP_ID_629636168 A-to-I Human chr17 + 62835600 62835599 62835601 CAGCCTGGGAGACAGAATGAGACCCTATCAAGAAAAAAAAAAAAAGAGGAGTGGAGAGAGATCAT CAGCCTGGGAGACAGAATGAGACCCTATCAAG__AAAAAAAAAAAGAGGAGTGGAGAGAGATCAT GAA G MARCHF10-DT Ensembl:ENSG00000265000 lincRNA exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs35098847 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_6659384 40847 RMVar_ID_40847 Human_SNP_ID_629636172 A-to-I Human chr17 + 62835600 62835600 62835600 CAGCCTGGGAGACAGAATGAGACCCTATCAAGAAAAAAAAAAAAAGAGGAGTGGAGAGAGATCAT CAGCCTGGGAGACAGAATGAGACCCTATCAAGGAAAAAAAAAAAAGAGGAGTGGAGAGAGATCAT A G MARCHF10-DT Ensembl:ENSG00000265000 lincRNA exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs75425302 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6659384 40848 RMVar_ID_40848 Human_SNP_ID_629713756 A-to-I Human chr17 + 63170367 63170367 63170367 TCAGGCAGGAGAATGGCGTGAACCCGGGAGGCAGAGCTTGCAGTAAGCCGAGATCGTGCCACTGC TCAGGCAGGAGAATGGCGTGAACCCGGGAGGCGGAGCTTGCAGTAAGCCGAGATCGTGCCACTGC A G TANC2 Ensembl:ENSG00000170921 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1195151177 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28512,RMVar_hsa_circ_36550,RMVar_hsa_circ_119468,RMVar_hsa_circ_306450,RMVar_hsa_circ_281653,RMVar_hsa_circ_186254,RMVar_hsa_circ_276051,RMVar_hsa_circ_91384,RMVar_hsa_circ_22942,RMVar_hsa_circ_186260,RMVar_hsa_circ_186261,RMVar_hsa_circ_330523,RMVar_hsa_circ_367933,RMVar_hsa_circ_85680,RMVar_hsa_circ_124492,RMVar_hsa_circ_81940,RMVar_hsa_circ_186263,RMVar_hsa_circ_186264,RMVar_hsa_circ_186262,RMVar_hsa_circ_186268,RMVar_hsa_circ_186269,RMVar_hsa_circ_186270 40849 RMVar_ID_40849 Human_SNP_ID_629776457 A-to-I Human chr17 - 63433234 63433233 63433235 AGGAGATCAAGACCATCCTGACTAACAAACACAGTGAAACCCCGTCTCTACTAAAAATACAAAAA AGGAGATCAAGACCATCCTGACTAACAAACA__GTGAAACCCCGTCTCTACTAAAAATACAAAAA CTG C CYB561 Ensembl:ENSG00000008283 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1317167467 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_132903 40850 RMVar_ID_40850 Human_SNP_ID_629811438 A-to-I Human chr17 + 63558035 63558035 63558035 GTCCCACCTCTGCCTCCCGAGTAGCTGAGACTACAGGTGCACACCACCACGCCCGCTAATTTTTG GTCCCACCTCTGCCTCCCGAGTAGCTGAGACTGCAGGTGCACACCACCACGCCCGCTAATTTTTG A G DCAF7 Ensembl:ENSG00000136485 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1030723888 Functional Loss SNV dbSNP153 33..33 33 - - - 40851 RMVar_ID_40851 Human_SNP_ID_629814038 A-to-I Human chr17 + 63568277 63568277 63568277 CCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAAGAGTGAGCCACCGTGCCCAGGTCTGATTTCG CCCGCCTCAGCCTCCCAAAGTGCTGGGATTACCAGAGTGAGCCACCGTGCCCAGGTCTGATTTCG A C DCAF7 Ensembl:ENSG00000136485 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264991118 Functional Loss SNV dbSNP153 33..33 33 - - - 40852 RMVar_ID_40852 Human_SNP_ID_629814405 A-to-I Human chr17 + 63569878 63569878 63569878 GGGATTACAGGTGTGCACCACCACGCTTTGCTAATCTTTGTATTTTTTGTAGAGACGGGCTTTCG GGGATTACAGGTGTGCACCACCACGCTTTGCTTATCTTTGTATTTTTTGTAGAGACGGGCTTTCG A T DCAF7 Ensembl:ENSG00000136485 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs776874194 Functional Loss SNV dbSNP153 33..33 33 - - - 40853 RMVar_ID_40853 Human_SNP_ID_629815035 A-to-I Human chr17 + 63572832 63572832 63572832 TTGCCCAGGCTGCAGTGTGGTGGCATGATCTCAGCTCACTGCAACCTCTACCTCCTAGGCTCAAA TTGCCCAGGCTGCAGTGTGGTGGCATGATCTCGGCTCACTGCAACCTCTACCTCCTAGGCTCAAA A G DCAF7 Ensembl:ENSG00000136485 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1047360149 Functional Loss SNV dbSNP153 33..33 33 - - - 40854 RMVar_ID_40854 Human_SNP_ID_629815036 A-to-I Human chr17 + 63572832 63572832 63572832 TTGCCCAGGCTGCAGTGTGGTGGCATGATCTCAGCTCACTGCAACCTCTACCTCCTAGGCTCAAA TTGCCCAGGCTGCAGTGTGGTGGCATGATCTCTGCTCACTGCAACCTCTACCTCCTAGGCTCAAA A T DCAF7 Ensembl:ENSG00000136485 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1047360149 Functional Loss SNV dbSNP153 33..33 33 - - - 40855 RMVar_ID_40855 Human_SNP_ID_629823445 A-to-I Human chr17 + 63608850 63608850 63608850 AGTGATAAGGGACTTGGCAGTGGCTCACACCTATAATCCCATCTACTCGAGAGGCTGAGGCGGGA AGTGATAAGGGACTTGGCAGTGGCTCACACCTGTAATCCCATCTACTCGAGAGGCTGAGGCGGGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1357126228 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6632125,Human_RBP_ID_26454328 40856 RMVar_ID_40856 Human_SNP_ID_629832022 A-to-I Human chr17 + 63645209 63645209 63645209 TAGAAACATGATAGACCTCGGGAGGCCGAGGCAAGAGAATCGTTTGAACCCGGGAGACGGAGGTT TAGAAACATGATAGACCTCGGGAGGCCGAGGCCAGAGAATCGTTTGAACCCGGGAGACGGAGGTT A C MAP3K3 Ensembl:ENSG00000198909 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1207724987 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112584,RMVar_hsa_circ_186320,RMVar_hsa_circ_349169,RMVar_hsa_circ_186319,RMVar_hsa_circ_356624,RMVar_hsa_circ_293103,RMVar_hsa_circ_186321,RMVar_hsa_circ_327930,RMVar_hsa_circ_186322,RMVar_hsa_circ_329400 40857 RMVar_ID_40857 Human_SNP_ID_629836260 A-to-I Human chr17 + 63662874 63662874 63662874 GAGATGGGGTTGGGCGGGGGGCGGTCCTCACCATGTTGGCCGGGCTGGTCTCGAACTCTTAAACT GAGATGGGGTTGGGCGGGGGGCGGTCCTCACCGTGTTGGCCGGGCTGGTCTCGAACTCTTAAACT A G MAP3K3 Ensembl:ENSG00000198909 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1177003092 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112584,RMVar_hsa_circ_18458,RMVar_hsa_circ_186319,RMVar_hsa_circ_356624,RMVar_hsa_circ_293103,RMVar_hsa_circ_329400,RMVar_hsa_circ_328761 40858 RMVar_ID_40858 Human_SNP_ID_629836261 A-to-I Human chr17 + 63662874 63662874 63662874 GAGATGGGGTTGGGCGGGGGGCGGTCCTCACCATGTTGGCCGGGCTGGTCTCGAACTCTTAAACT GAGATGGGGTTGGGCGGGGGGCGGTCCTCACCTTGTTGGCCGGGCTGGTCTCGAACTCTTAAACT A T MAP3K3 Ensembl:ENSG00000198909 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1177003092 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112584,RMVar_hsa_circ_18458,RMVar_hsa_circ_186319,RMVar_hsa_circ_356624,RMVar_hsa_circ_293103,RMVar_hsa_circ_329400,RMVar_hsa_circ_328761 40859 RMVar_ID_40859 Human_SNP_ID_629837978 A-to-I Human chr17 + 63670444 63670444 63670444 GTCACTAATAAAAATGCAAAAATTAGCTGGGCATGATGGTGAGTGCCTCTAGTCCCAGCTACTCA GTCACTAATAAAAATGCAAAAATTAGCTGGGCGTGATGGTGAGTGCCTCTAGTCCCAGCTACTCA A G MAP3K3 Ensembl:ENSG00000198909 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1483007403 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22586649 RMVar_hsa_circ_18458,RMVar_hsa_circ_356624,RMVar_hsa_circ_329400,RMVar_hsa_circ_21689 40860 RMVar_ID_40860 Human_SNP_ID_629838951 A-to-I Human chr17 + 63674603 63674603 63674603 ATTCCTGGTCTCAAGCAATCCTTCTACACCTCAGCTTCCCAAAGTGCTGAGATTATAGGTATGAG ATTCCTGGTCTCAAGCAATCCTTCTACACCTCCGCTTCCCAAAGTGCTGAGATTATAGGTATGAG A C MAP3K3 Ensembl:ENSG00000198909 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1451009142 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18458,RMVar_hsa_circ_356624,RMVar_hsa_circ_329400,RMVar_hsa_circ_21689 40861 RMVar_ID_40861 Human_SNP_ID_629840048 A-to-I Human chr17 + 63679519 63679519 63679519 GTTGTTTTGTCTATGAGACAGGGTCGCACTCTATCACCTATGCTGGAGTGCAGTGGTCCAAACAC GTTGTTTTGTCTATGAGACAGGGTCGCACTCTGTCACCTATGCTGGAGTGCAGTGGTCCAAACAC A G MAP3K3 Ensembl:ENSG00000198909 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048114056 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18458,RMVar_hsa_circ_356624,RMVar_hsa_circ_329400,RMVar_hsa_circ_21689 40862 RMVar_ID_40862 Human_SNP_ID_629851643 A-to-I Human chr17 - 63725534 63725534 63725534 CAGGCTGGCCAACGTGGTGAAACCACATCTCTACTAAAAATACAAAAATTAGCCGGGCATGGTGA CAGGCTGGCCAACGTGGTGAAACCACATCTCTGCTAAAAATACAAAAATTAGCCGGGCATGGTGA T C STRADA,AC046185.1 Ensembl:ENSG00000266173,Ensembl:ENSG00000125695 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1166640133 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25315946 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 40863 RMVar_ID_40863 Human_SNP_ID_629852578 A-to-I Human chr17 - 63729702 63729702 63729702 TCACTGCAACCTCTGCCTCCTGGGTTCAAGCAATTCTTCTTTCTCAGCCTCCTGAGTAGCTGGGA TCACTGCAACCTCTGCCTCCTGGGTTCAAGCAGTTCTTCTTTCTCAGCCTCCTGAGTAGCTGGGA T C STRADA,AC046185.1 Ensembl:ENSG00000266173,Ensembl:ENSG00000125695 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1315465688 Functional Loss SNV dbSNP153 33..33 33 - - - 40864 RMVar_ID_40864 Human_SNP_ID_629853408 A-to-I Human chr17 - 63732640 63732640 63732640 CAGGCACATGCCACCATGCCTGGCTAATTTTTATATTTTTGTAGAGATGGGCTTTCGCCATGTTG CAGGCACATGCCACCATGCCTGGCTAATTTTTCTATTTTTGTAGAGATGGGCTTTCGCCATGTTG T G STRADA,AC046185.1 Ensembl:ENSG00000266173,Ensembl:ENSG00000125695 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs906429023 Functional Loss SNV dbSNP153 33..33 33 - - - 40865 RMVar_ID_40865 Human_SNP_ID_629853416 A-to-I Human chr17 - 63732673 63732673 63732673 CTCCCACCTCACCCTCCCAAGTAGTTGGGACTACAGGCACATGCCACCATGCCTGGCTAATTTTT CTCCCACCTCACCCTCCCAAGTAGTTGGGACTGCAGGCACATGCCACCATGCCTGGCTAATTTTT T C STRADA,AC046185.1 Ensembl:ENSG00000266173,Ensembl:ENSG00000125695 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1235779281 Functional Loss SNV dbSNP153 33..33 33 - - - 40866 RMVar_ID_40866 Human_SNP_ID_629853450 A-to-I Human chr17 - 63732828 63732828 63732828 CTGTTAGTCTCACCACTTTGGGAGGCCAAGGTAGGAGAATCACTTGAGCCCAGGAGTTCAAGACC CTGTTAGTCTCACCACTTTGGGAGGCCAAGGTGGGAGAATCACTTGAGCCCAGGAGTTCAAGACC T C STRADA,AC046185.1 Ensembl:ENSG00000266173,Ensembl:ENSG00000125695 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1226195468 Functional Loss SNV dbSNP153 33..33 33 - - - 40867 RMVar_ID_40867 Human_SNP_ID_629853782 A-to-I Human chr17 - 63734496 63734496 63734496 GCAATTACAGGCCAGTGCCACCATGCCCGGCTAATTTTTGTATTTTTTATAGAGATGGGGTTTTC GCAATTACAGGCCAGTGCCACCATGCCCGGCTGATTTTTGTATTTTTTATAGAGATGGGGTTTTC T C STRADA,AC046185.1 Ensembl:ENSG00000266173,Ensembl:ENSG00000125695 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1451393663 Functional Loss SNV dbSNP153 33..33 33 - - - 40868 RMVar_ID_40868 Human_SNP_ID_629853808 A-to-I Human chr17 - 63734590 63734590 63734590 CTCTGTCATCCAGGCTGGAGTGCAGTGGCGCAATCTCGGCTCACTGCAACCTCTGCCTCCCGAGT CTCTGTCATCCAGGCTGGAGTGCAGTGGCGCAGTCTCGGCTCACTGCAACCTCTGCCTCCCGAGT T C STRADA,AC046185.1 Ensembl:ENSG00000266173,Ensembl:ENSG00000125695 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs989179354 Functional Loss SNV dbSNP153 33..33 33 - - - 40869 RMVar_ID_40869 Human_SNP_ID_629854155 A-to-I Human chr17 - 63736079 63736079 63736079 AAATCAGCCGGGCGTAGTGGCACATGCCAGTAATCCCAGCTACTCCGGAGGCTGAGGCAGGAGAA AAATCAGCCGGGCGTAGTGGCACATGCCAGTAGTCCCAGCTACTCCGGAGGCTGAGGCAGGAGAA T C STRADA,AC046185.1 Ensembl:ENSG00000266173,Ensembl:ENSG00000125695 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1375822888 Functional Loss SNV dbSNP153 33..33 33 - - - 40870 RMVar_ID_40870 Human_SNP_ID_629854245 A-to-I Human chr17 - 63736456 63736454 63736456 GCCTGGCTAATTATTGTATTTTTAGTAGAGACAGTGTTTTGCAATGTTGGGCAGGCTGGTCTCAA GCCTGGCTAATTATTGTATTTTTAGTAGAGAC__TGTTTTGCAATGTTGGGCAGGCTGGTCTCAA ACT A STRADA,AC046185.1 Ensembl:ENSG00000266173,Ensembl:ENSG00000125695 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1327951142 Functional Loss DEL dbSNP153 33..34 33 - - - 40871 RMVar_ID_40871 Human_SNP_ID_629854419 A-to-I Human chr17 - 63737032 63737032 63737032 GTTGACTAGACTGGTCTTGAACTCCTGACCTCAGGTGATCTGCCCTCCTCAGCCTCCCAAAGTGC GTTGACTAGACTGGTCTTGAACTCCTGACCTCGGGTGATCTGCCCTCCTCAGCCTCCCAAAGTGC T C STRADA,AC046185.1 Ensembl:ENSG00000266173,Ensembl:ENSG00000125695 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1177751720 Functional Loss SNV dbSNP153 33..33 33 - - - 40872 RMVar_ID_40872 Human_SNP_ID_629857501 A-to-I Human chr17 - 63747971 63747971 63747971 ACATGCCTGTAATCCCAGCTACTCGGGAGGCTAAGGCAGGAGAATGGCTTGAACCCGGAAGGCAG ACATGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCTTGAACCCGGAAGGCAG T C AC046185.1,CCDC47 Ensembl:ENSG00000125695,Ensembl:ENSG00000108588 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946182152 Functional Loss SNV dbSNP153 33..33 33 - - - 40873 RMVar_ID_40873 Human_SNP_ID_629858285 A-to-I Human chr17 - 63751013 63751013 63751013 AAAATTAGCTGTGCATAGTGGTGCATACCTGTAGTCCCAACTACTTGGGAGACTGAAGTGGAAGG AAAATTAGCTGTGCATAGTGGTGCATACCTGTCGTCCCAACTACTTGGGAGACTGAAGTGGAAGG T G AC046185.1,CCDC47 Ensembl:ENSG00000125695,Ensembl:ENSG00000108588 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs902576156 Functional Loss SNV dbSNP153 33..33 33 - - - 40874 RMVar_ID_40874 Human_SNP_ID_629867668 A-to-I Human chr17 + 63783801 63783801 63783801 TAATACTAAGCAGCCTGGGTGCCGTGGCTCACACCTGTAATCCCAGCACTTCGGGAGGCCAAGGT TAATACTAAGCAGCCTGGGTGCCGTGGCTCACGCCTGTAATCCCAGCACTTCGGGAGGCCAAGGT A G DDX42 Ensembl:ENSG00000198231 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1186035247 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3944,RMVar_hsa_circ_35122,RMVar_hsa_circ_186344,RMVar_hsa_circ_94895,RMVar_hsa_circ_268145,RMVar_hsa_circ_362359,RMVar_hsa_circ_53854,RMVar_hsa_circ_18183 40875 RMVar_ID_40875 Human_SNP_ID_629868692 A-to-I Human chr17 + 63787691 63787691 63787691 TGAAACCCTGTCTACTAAAAATACAAAACATTAGCCAGGCGTGGTGGTGCACGCCTATAATCCCA TGAAACCCTGTCTACTAAAAATACAAAACATTGGCCAGGCGTGGTGGTGCACGCCTATAATCCCA A G DDX42 Ensembl:ENSG00000198231 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1406663967 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3944,RMVar_hsa_circ_186344,RMVar_hsa_circ_94895,RMVar_hsa_circ_268145,RMVar_hsa_circ_362359,RMVar_hsa_circ_53854,RMVar_hsa_circ_18183,RMVar_hsa_circ_42872,RMVar_hsa_circ_324967,RMVar_hsa_circ_61148,RMVar_hsa_circ_9421,RMVar_hsa_circ_186346 40876 RMVar_ID_40876 Human_SNP_ID_629868698 A-to-I Human chr17 + 63787715 63787715 63787715 AAAACATTAGCCAGGCGTGGTGGTGCACGCCTATAATCCCAACTACTCAGGAGGAGGCTGAGGCA AAAACATTAGCCAGGCGTGGTGGTGCACGCCTGTAATCCCAACTACTCAGGAGGAGGCTGAGGCA A G DDX42 Ensembl:ENSG00000198231 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs528631002 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3944,RMVar_hsa_circ_186344,RMVar_hsa_circ_94895,RMVar_hsa_circ_268145,RMVar_hsa_circ_362359,RMVar_hsa_circ_53854,RMVar_hsa_circ_18183,RMVar_hsa_circ_42872,RMVar_hsa_circ_324967,RMVar_hsa_circ_61148,RMVar_hsa_circ_9421,RMVar_hsa_circ_186346 40877 RMVar_ID_40877 Human_SNP_ID_629868699 A-to-I Human chr17 + 63787717 63787717 63787717 AACATTAGCCAGGCGTGGTGGTGCACGCCTATAATCCCAACTACTCAGGAGGAGGCTGAGGCAGG AACATTAGCCAGGCGTGGTGGTGCACGCCTATGATCCCAACTACTCAGGAGGAGGCTGAGGCAGG A G DDX42 Ensembl:ENSG00000198231 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1034642947 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3944,RMVar_hsa_circ_186344,RMVar_hsa_circ_94895,RMVar_hsa_circ_268145,RMVar_hsa_circ_362359,RMVar_hsa_circ_53854,RMVar_hsa_circ_18183,RMVar_hsa_circ_42872,RMVar_hsa_circ_324967,RMVar_hsa_circ_61148,RMVar_hsa_circ_9421,RMVar_hsa_circ_186346 40878 RMVar_ID_40878 Human_SNP_ID_629869040 A-to-I Human chr17 + 63788558 63788558 63788558 TCAATCTCCTGACCTCATGATCCGCCCGCCTCAGCCTCCCAAACTGCTAGGATTATACAGGCGTG TCAATCTCCTGACCTCATGATCCGCCCGCCTCGGCCTCCCAAACTGCTAGGATTATACAGGCGTG A G DDX42 Ensembl:ENSG00000198231 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs573182777 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3944,RMVar_hsa_circ_186344,RMVar_hsa_circ_94895,RMVar_hsa_circ_268145,RMVar_hsa_circ_362359,RMVar_hsa_circ_53854,RMVar_hsa_circ_18183,RMVar_hsa_circ_42872,RMVar_hsa_circ_324967,RMVar_hsa_circ_61148,RMVar_hsa_circ_9421,RMVar_hsa_circ_186346 40879 RMVar_ID_40879 Human_SNP_ID_629869148 A-to-I Human chr17 + 63788918 63788918 63788918 GTTTTGTTTTGTTTTTGTTGTTGTTTTGAGATAGGGTCTCACTCTGTCACCCAGGCTGGAGTGGA GTTTTGTTTTGTTTTTGTTGTTGTTTTGAGATGGGGTCTCACTCTGTCACCCAGGCTGGAGTGGA A G DDX42 Ensembl:ENSG00000198231 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1567732431 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3944,RMVar_hsa_circ_186344,RMVar_hsa_circ_94895,RMVar_hsa_circ_268145,RMVar_hsa_circ_362359,RMVar_hsa_circ_53854,RMVar_hsa_circ_18183,RMVar_hsa_circ_42872,RMVar_hsa_circ_324967,RMVar_hsa_circ_61148,RMVar_hsa_circ_9421,RMVar_hsa_circ_186346 40880 RMVar_ID_40880 Human_SNP_ID_629869699 A-to-I Human chr17 + 63790469 63790469 63790469 CAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTGGTCTGGGCATGGTGGCTCAAACC CAACATGGTGAAACCCCGTCTCTACTAAAAATGCAAAAATTGGTCTGGGCATGGTGGCTCAAACC A G DDX42 Ensembl:ENSG00000198231 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1053761635 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13128495 RMVar_hsa_circ_3944,RMVar_hsa_circ_186344,RMVar_hsa_circ_94895,RMVar_hsa_circ_268145,RMVar_hsa_circ_362359,RMVar_hsa_circ_53854,RMVar_hsa_circ_18183,RMVar_hsa_circ_42872,RMVar_hsa_circ_324967,RMVar_hsa_circ_61148,RMVar_hsa_circ_9421,RMVar_hsa_circ_186346 40881 RMVar_ID_40881 Human_SNP_ID_629869746 A-to-I Human chr17 + 63790639 63790639 63790639 AAAAATTAGCTGGGTGTGGTGGCGGCGCATATAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGA AAAAATTAGCTGGGTGTGGTGGCGGCGCATATGATCCCAGCTACTTGGGAGGCTGAGGCAGGAGA A G DDX42 Ensembl:ENSG00000198231 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs953129032 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3944,RMVar_hsa_circ_186344,RMVar_hsa_circ_94895,RMVar_hsa_circ_268145,RMVar_hsa_circ_362359,RMVar_hsa_circ_53854,RMVar_hsa_circ_18183,RMVar_hsa_circ_42872,RMVar_hsa_circ_324967,RMVar_hsa_circ_61148,RMVar_hsa_circ_9421,RMVar_hsa_circ_186346 40882 RMVar_ID_40882 Human_SNP_ID_629869964 A-to-I Human chr17 + 63791511 63791511 63791511 TTTTGTATTTTTAGTAGACACAGGGTTTCACCATGTTGGCTGGGCTGGTCTCAAACTCTTGACAT TTTTGTATTTTTAGTAGACACAGGGTTTCACCGTGTTGGCTGGGCTGGTCTCAAACTCTTGACAT A G DDX42 Ensembl:ENSG00000198231 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs146099551 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3944,RMVar_hsa_circ_186344,RMVar_hsa_circ_94895,RMVar_hsa_circ_268145,RMVar_hsa_circ_362359,RMVar_hsa_circ_53854,RMVar_hsa_circ_18183,RMVar_hsa_circ_42872,RMVar_hsa_circ_324967,RMVar_hsa_circ_61148,RMVar_hsa_circ_9421,RMVar_hsa_circ_186346 40883 RMVar_ID_40883 Human_SNP_ID_629881926 A-to-I Human chr17 + 63831735 63831735 63831735 CAATTTCCTTTTCCTGTTCAGGGCGTGTGCACAGAAGCTGGCATGTATGCCCTGCGAGAACGGCG CAATTTCCTTTTCCTGTTCAGGGCGTGTGCACGGAAGCTGGCATGTATGCCCTGCGAGAACGGCG A G PSMC5 Ensembl:ENSG00000087191 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1131321 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_497125,Human_RBP_ID_896776,Human_RBP_ID_4445205,Human_RBP_ID_5115599,Human_RBP_ID_18988992,Human_RBP_ID_22444847 Human_Splice_Rec_1853654,Human_Splice_Rec_1853655,Human_Splice_Rec_1853740,Human_Splice_Rec_1853741,Human_Splice_Rec_1853764,Human_Splice_Rec_1853765,Human_Splice_Rec_1853796,Human_Splice_Rec_1853797,Human_Splice_Rec_1853818,Human_Splice_Rec_1853819,Human_Splice_Rec_1853840,Human_Splice_Rec_1853841,Human_Splice_Rec_1853862,Human_Splice_Rec_1853863,Human_Splice_Rec_1853887 Human_miRNA_ID_2696173 RMVar_hsa_circ_98129,RMVar_hsa_circ_86525,RMVar_hsa_circ_186378,RMVar_hsa_circ_186381 40884 RMVar_ID_40884 Human_SNP_ID_629882912 A-to-I Human chr17 - 63834719 63834719 63834719 TTGAGCTGGACAAGGAGCTGTACGGGCCTGACAATCACCTGGTGGAGGTGAGAGTGGGCCTGGGG TTGAGCTGGACAAGGAGCTGTACGGGCCTGACGATCACCTGGTGGAGGTGAGAGTGGGCCTGGGG T C SMARCD2 Ensembl:ENSG00000108604 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1130100 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_497163,Human_RBP_ID_902682,Human_RBP_ID_3950951,Human_RBP_ID_8821284,Human_RBP_ID_9376610,Human_RBP_ID_17493255,Human_RBP_ID_18705942,Human_RBP_ID_18988995,Human_RBP_ID_22445693 Human_Splice_Rec_1853898,Human_Splice_Rec_1853899,Human_Splice_Rec_1853922,Human_Splice_Rec_1853923,Human_Splice_Rec_1853946,Human_Splice_Rec_1853947,Human_Splice_Rec_1853970,Human_Splice_Rec_1853971,Human_Splice_Rec_1853985,Human_Splice_Rec_1853997,Human_Splice_Rec_1854012,Human_Splice_Rec_1854013,Human_Splice_Rec_1854020,Human_Splice_Rec_1854021,Human_Splice_Rec_1854025 Human_miRNA_ID_2239796,Human_miRNA_ID_2704819,Human_miRNA_ID_3017092 RMVar_hsa_circ_115597,RMVar_hsa_circ_186386,RMVar_hsa_circ_71776,RMVar_hsa_circ_20330 40885 RMVar_ID_40885 Human_SNP_ID_629883370 A-to-I Human chr17 - 63836382 63836382 63836382 TAATTCTTCTTGCCTCAGCCTCCCGAGTAACTAGGATTACAGATGCCTGTCACCACGCCCGGCTA TAATTCTTCTTGCCTCAGCCTCCCGAGTAACTGGGATTACAGATGCCTGTCACCACGCCCGGCTA T C SMARCD2 Ensembl:ENSG00000108604 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1467925228 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8460324 RMVar_hsa_circ_71776,RMVar_hsa_circ_360600 40886 RMVar_ID_40886 Human_SNP_ID_629884374 A-to-I Human chr17 - 63840066 63840066 63840066 GGAGTGCAGTGACATGATCTCAGCTCACTGCAACCTCCGCCTCCCAGGTTCAAACAATCCTCTGC GGAGTGCAGTGACATGATCTCAGCTCACTGCAGCCTCCGCCTCCCAGGTTCAAACAATCCTCTGC T C SMARCD2 Ensembl:ENSG00000108604 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042976558 Functional Loss SNV dbSNP153 33..33 33 - - - 40887 RMVar_ID_40887 Human_SNP_ID_629884375 A-to-I Human chr17 - 63840066 63840066 63840066 GGAGTGCAGTGACATGATCTCAGCTCACTGCAACCTCCGCCTCCCAGGTTCAAACAATCCTCTGC GGAGTGCAGTGACATGATCTCAGCTCACTGCACCCTCCGCCTCCCAGGTTCAAACAATCCTCTGC T G SMARCD2 Ensembl:ENSG00000108604 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042976558 Functional Loss SNV dbSNP153 33..33 33 - - - 40888 RMVar_ID_40888 Human_SNP_ID_629884462 A-to-I Human chr17 - 63840373 63840373 63840373 GACCAGGAGTTCAAGACCAGCCTAAGCAACATAGTGAGACCATCATCTCTTAAAAAAAAAAAAAA GACCAGGAGTTCAAGACCAGCCTAAGCAACATGGTGAGACCATCATCTCTTAAAAAAAAAAAAAA T C SMARCD2 Ensembl:ENSG00000108604 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1010989903 Functional Loss SNV dbSNP153 33..33 33 - - - 40889 RMVar_ID_40889 Human_SNP_ID_629938750 A-to-I Human chr17 - 64018971 64018971 64018971 TCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGAGGATCATGAGGTCAAGAGATAGAG TCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGAGGATCATGAGGTCAAGAGATAGAG T C ICAM2 Ensembl:ENSG00000108622 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4968689 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90886,RMVar_hsa_circ_186395 40890 RMVar_ID_40890 Human_SNP_ID_629965259 A-to-I Human chr17 - 64128097 64128097 64128097 CCAGCTACTGGGGAGGCTGAGGCAGGAGAATCACCCGAACCTGGGAGGCAGAGGTTGCAGAGATG CCAGCTACTGGGGAGGCTGAGGCAGGAGAATCGCCCGAACCTGGGAGGCAGAGGTTGCAGAGATG T C ERN1 Ensembl:ENSG00000178607 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1020052273 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112217,RMVar_hsa_circ_186400 40891 RMVar_ID_40891 Human_SNP_ID_630010801 A-to-I Human chr17 - 64322223 64322222 64322223 TGTCACCACGCCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCACGTTGGCCAGGC TGTCACCACGCCTGGCTAATTTTTGTATTTTT_GTAGAGATGGGGTTTCACCACGTTGGCCAGGC CT C PECAM1 Ensembl:ENSG00000261371 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs554996720 Functional Loss DEL dbSNP153 33..33 33 - - - 40892 RMVar_ID_40892 Human_SNP_ID_630010812 A-to-I Human chr17 - 64322256 64322252 64322256 TCAGCCTCCCGAGTAGCTGGGATTACAGGCACATGTCACCACGCCTGGCTAATTTTTGTATTTTT TCAGCCTCCCGAGTAGCTGGGATTACAGGCAC____CACCACGCCTGGCTAATTTTTGTATTTTT GACAT G PECAM1 Ensembl:ENSG00000261371 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1342015704 Functional Loss DEL dbSNP153 33..36 33 - - - 40893 RMVar_ID_40893 Human_SNP_ID_630040862 A-to-I Human chr17 + 64467792 64467792 64467792 CCCCATCTCTACTAAAAATACAAAAATTAGCCAGGTGTGGTGGTGTGTGTGTGTAGTCCCAGCTA CCCCATCTCTACTAAAAATACAAAAATTAGCCGGGTGTGGTGGTGTGTGTGTGTAGTCCCAGCTA A G MILR1 Ensembl:ENSG00000271605 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs767776618 Functional Loss SNV dbSNP153 33..33 33 - - - 40894 RMVar_ID_40894 Human_SNP_ID_630041033 A-to-I Human chr17 + 64468347 64468347 64468347 GTCTCACTCTGTTGCCCAGGCTGGAGTTCAGTAGCGCGATCTTGGCTCACTTCAATCTCCATCTT GTCTCACTCTGTTGCCCAGGCTGGAGTTCAGTGGCGCGATCTTGGCTCACTTCAATCTCCATCTT A G MILR1 Ensembl:ENSG00000271605 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1296240603 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1854872,Human_Splice_Rec_1854920 40895 RMVar_ID_40895 Human_SNP_ID_630044559 A-to-I Human chr17 - 64483334 64483334 64483334 TTTTTGTATTTTTTTGGTAGAGAGAAGTTTTCACCGTGTTGCCCAGGCTGGTCTCAAACTCCTGA TTTTTGTATTTTTTTGGTAGAGAGAAGTTTTCGCCGTGTTGCCCAGGCTGGTCTCAAACTCCTGA T C POLG2 Ensembl:ENSG00000256525 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1304104857 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_186424,RMVar_hsa_circ_354395,RMVar_hsa_circ_186423,RMVar_hsa_circ_276195,RMVar_hsa_circ_186422,RMVar_hsa_circ_186426,RMVar_hsa_circ_287644,RMVar_hsa_circ_332049,RMVar_hsa_circ_186425 40896 RMVar_ID_40896 Human_SNP_ID_630044740 A-to-I Human chr17 - 64483988 64483988 64483988 AGAGAAGGCTGGGCTGAATGGCTCACGCCTATAATCCCAGCACTTTGGGAAGCCAAGGTGGGTGG AGAGAAGGCTGGGCTGAATGGCTCACGCCTATCATCCCAGCACTTTGGGAAGCCAAGGTGGGTGG T G POLG2 Ensembl:ENSG00000256525 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs1288047554 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1854971,Human_Splice_Rec_1855009 RMVar_hsa_circ_186424,RMVar_hsa_circ_354395,RMVar_hsa_circ_186423,RMVar_hsa_circ_276195,RMVar_hsa_circ_186422,RMVar_hsa_circ_186426,RMVar_hsa_circ_287644,RMVar_hsa_circ_332049,RMVar_hsa_circ_186425 40897 RMVar_ID_40897 Human_SNP_ID_630044741 A-to-I Human chr17 - 64483990 64483990 64483990 GAAGAGAAGGCTGGGCTGAATGGCTCACGCCTATAATCCCAGCACTTTGGGAAGCCAAGGTGGGT GAAGAGAAGGCTGGGCTGAATGGCTCACGCCTGTAATCCCAGCACTTTGGGAAGCCAAGGTGGGT T C POLG2 Ensembl:ENSG00000256525 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1230089177 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1854971,Human_Splice_Rec_1855009 RMVar_hsa_circ_186424,RMVar_hsa_circ_354395,RMVar_hsa_circ_186423,RMVar_hsa_circ_276195,RMVar_hsa_circ_186422,RMVar_hsa_circ_186426,RMVar_hsa_circ_287644,RMVar_hsa_circ_332049,RMVar_hsa_circ_186425 40898 RMVar_ID_40898 Human_SNP_ID_630045320 A-to-I Human chr17 - 64486477 64486477 64486477 TGTGCCTGTAGTCCTAGCTACTCAGGAGACTGAGGCAAGAGAATCACTTGAACCCGGGTGGCAGA TGTGCCTGTAGTCCTAGCTACTCAGGAGACTGGGGCAAGAGAATCACTTGAACCCGGGTGGCAGA T C POLG2 Ensembl:ENSG00000256525 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1453849681 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13130119 RMVar_hsa_circ_354395,RMVar_hsa_circ_186423,RMVar_hsa_circ_186426,RMVar_hsa_circ_332049,RMVar_hsa_circ_186425,RMVar_hsa_circ_347556 40899 RMVar_ID_40899 Human_SNP_ID_630045541 A-to-I Human chr17 - 64487422 64487422 64487422 TTTAGTAGAGGTGGGGTTTTACCATGTTGGCCAGGCTGGTCTCGAACTCCTGAACTCAAGTGATT TTTAGTAGAGGTGGGGTTTTACCATGTTGGCCCGGCTGGTCTCGAACTCCTGAACTCAAGTGATT T G POLG2 Ensembl:ENSG00000256525 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1468385900 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_354395,RMVar_hsa_circ_186423,RMVar_hsa_circ_186426,RMVar_hsa_circ_332049,RMVar_hsa_circ_186425,RMVar_hsa_circ_347556 40900 RMVar_ID_40900 Human_SNP_ID_630045555 A-to-I Human chr17 - 64487532 64487532 64487532 TCTGCTCACTGCAGCCTCCACCTCCTGGGTTCAAGTGATTCTCATGCCTCAGCCTGCTGAGTAGC TCTGCTCACTGCAGCCTCCACCTCCTGGGTTCGAGTGATTCTCATGCCTCAGCCTGCTGAGTAGC T C POLG2 Ensembl:ENSG00000256525 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1030122100 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_354395,RMVar_hsa_circ_186423,RMVar_hsa_circ_186426,RMVar_hsa_circ_332049,RMVar_hsa_circ_186425,RMVar_hsa_circ_347556 40901 RMVar_ID_40901 Human_SNP_ID_630045850 A-to-I Human chr17 - 64488783 64488783 64488783 TTGTATTTTTAGTAGAGACAGGGTTTCACCATATTGACCAGGCTGGAATTTTTAAATATGAATAA TTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGACCAGGCTGGAATTTTTAAATATGAATAA T C POLG2 Ensembl:ENSG00000256525 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1568087081 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13130233 RMVar_hsa_circ_354395,RMVar_hsa_circ_186423,RMVar_hsa_circ_186426,RMVar_hsa_circ_332049,RMVar_hsa_circ_186425,RMVar_hsa_circ_347556 40902 RMVar_ID_40902 Human_SNP_ID_630045856 A-to-I Human chr17 - 64488805 64488805 64488805 CGCCACCACGCCCGGTTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATATTGACCAGGC CGCCACCACGCCCGGTTAATTTTTGTATTTTTGGTAGAGACAGGGTTTCACCATATTGACCAGGC T C POLG2 Ensembl:ENSG00000256525 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1465668311 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_354395,RMVar_hsa_circ_186423,RMVar_hsa_circ_186426,RMVar_hsa_circ_332049,RMVar_hsa_circ_186425,RMVar_hsa_circ_347556 40903 RMVar_ID_40903 Human_SNP_ID_630045876 A-to-I Human chr17 - 64488885 64488885 64488885 GCTGGAGTGCAGTGTCGCGATTCCCAGGTTCAAGCAGTTCTTCTGCCTCAGCCTCCTGAGTAGCT GCTGGAGTGCAGTGTCGCGATTCCCAGGTTCAGGCAGTTCTTCTGCCTCAGCCTCCTGAGTAGCT T C POLG2 Ensembl:ENSG00000256525 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1226350368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1854966,Human_Splice_Rec_1854967 RMVar_hsa_circ_354395,RMVar_hsa_circ_186423,RMVar_hsa_circ_186426,RMVar_hsa_circ_332049,RMVar_hsa_circ_186425,RMVar_hsa_circ_347556 40904 RMVar_ID_40904 Human_SNP_ID_630045895 A-to-I Human chr17 - 64488931 64488931 64488931 TTTTATTTTTTTATTTTTTGAGACAGCATCTCACTCTGTTGCCCAGGCTGGAGTGCAGTGTCGCG TTTTATTTTTTTATTTTTTGAGACAGCATCTCTCTCTGTTGCCCAGGCTGGAGTGCAGTGTCGCG T A POLG2 Ensembl:ENSG00000256525 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1382800401 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1854966,Human_Splice_Rec_1854967 RMVar_hsa_circ_354395,RMVar_hsa_circ_186423,RMVar_hsa_circ_186426,RMVar_hsa_circ_332049,RMVar_hsa_circ_186425,RMVar_hsa_circ_347556 40905 RMVar_ID_40905 Human_SNP_ID_630046107 A-to-I Human chr17 - 64489644 64489644 64489644 CAAGCAATCCTGCCTCAGCCTCCCAAGTAGCTAGGACTACAAGCATGTATCACCATGCCCGACTG CAAGCAATCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAAGCATGTATCACCATGCCCGACTG T C POLG2 Ensembl:ENSG00000256525 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs940692786 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13130277 RMVar_hsa_circ_354395,RMVar_hsa_circ_186423,RMVar_hsa_circ_186426,RMVar_hsa_circ_332049,RMVar_hsa_circ_186425,RMVar_hsa_circ_347556 40906 RMVar_ID_40906 Human_SNP_ID_630046126 A-to-I Human chr17 - 64489738 64489738 64489738 TTTTTTCTTTATTTGAGACAGGATCTCACTCTATCACTCAGGCTGAAACACAGTGGTATGGTGAT TTTTTTCTTTATTTGAGACAGGATCTCACTCTGTCACTCAGGCTGAAACACAGTGGTATGGTGAT T C POLG2 Ensembl:ENSG00000256525 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1019336856 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17566113 RMVar_hsa_circ_354395,RMVar_hsa_circ_186423,RMVar_hsa_circ_186426,RMVar_hsa_circ_332049,RMVar_hsa_circ_186425,RMVar_hsa_circ_347556 40907 RMVar_ID_40907 Human_SNP_ID_630046133 A-to-I Human chr17 - 64489760 64489756 64489760 GGTTTGCCAAATGGTGATTTTTTTTTTTCTTTATTTGAGACAGGATCTCACTCTATCACTCAGGC GGTTTGCCAAATGGTGATTTTTTTTTTTCTTT____GAGACAGGATCTCACTCTATCACTCAGGC CAAAT C POLG2 Ensembl:ENSG00000256525 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1381213711 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_13130279,Human_RBP_ID_17566114 RMVar_hsa_circ_354395,RMVar_hsa_circ_186423,RMVar_hsa_circ_186426,RMVar_hsa_circ_332049,RMVar_hsa_circ_186425,RMVar_hsa_circ_347556 40908 RMVar_ID_40908 Human_SNP_ID_630046135 A-to-I Human chr17 - 64489760 64489760 64489760 GGTTTGCCAAATGGTGATTTTTTTTTTTCTTTATTTGAGACAGGATCTCACTCTATCACTCAGGC GGTTTGCCAAATGGTGATTTTTTTTTTTCTTTTTTTGAGACAGGATCTCACTCTATCACTCAGGC T A POLG2 Ensembl:ENSG00000256525 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1555668166 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13130279,Human_RBP_ID_17566114 RMVar_hsa_circ_354395,RMVar_hsa_circ_186423,RMVar_hsa_circ_186426,RMVar_hsa_circ_332049,RMVar_hsa_circ_186425,RMVar_hsa_circ_347556 40909 RMVar_ID_40909 Human_SNP_ID_630046136 A-to-I Human chr17 - 64489760 64489760 64489760 GGTTTGCCAAATGGTGATTTTTTTTTTTCTTTATTTGAGACAGGATCTCACTCTATCACTCAGGC GGTTTGCCAAATGGTGATTTTTTTTTTTCTTTGTTTGAGACAGGATCTCACTCTATCACTCAGGC T C POLG2 Ensembl:ENSG00000256525 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1555668166 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13130279,Human_RBP_ID_17566114 RMVar_hsa_circ_354395,RMVar_hsa_circ_186423,RMVar_hsa_circ_186426,RMVar_hsa_circ_332049,RMVar_hsa_circ_186425,RMVar_hsa_circ_347556 40910 RMVar_ID_40910 Human_SNP_ID_630046222 A-to-I Human chr17 - 64490063 64490063 64490063 AAAATTAGCTGGATGTGGTGGCTTGCCCTTATAGTCTCAGCTACTTGGGAGGCTGAGGCAGGAGA AAAATTAGCTGGATGTGGTGGCTTGCCCTTATTGTCTCAGCTACTTGGGAGGCTGAGGCAGGAGA T A POLG2 Ensembl:ENSG00000256525 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs782253186 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_354395,RMVar_hsa_circ_186423,RMVar_hsa_circ_186426,RMVar_hsa_circ_332049,RMVar_hsa_circ_186425,RMVar_hsa_circ_347556 40911 RMVar_ID_40911 Human_SNP_ID_630047654 A-to-I Human chr17 - 64495496 64495473 64495497 CATGGCTCACTGCAGCCTCGACCTCGGGCTCAAGTGAACCTCCCACCTCAGCCTCCCAAGTAGCT CATGGCTCACTGCAGCCTCGACCTCGGGCTC________________________CCAAGTAGCT GGAGGCTGAGGTGGGAGGTTCACTT G POLG2 Ensembl:ENSG00000256525 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1555669347 Functional Loss DEL dbSNP153 32..55 33 - - - 40912 RMVar_ID_40912 Human_SNP_ID_630047677 A-to-I Human chr17 - 64495563 64495559 64495563 GAATTGGTAAATTAAAATTGAATATGGGTCTCACTCTGTCACCCAGACTCGAGTGCAGTGGTGTG GAATTGGTAAATTAAAATTGAATATGGGTCTC____TGTCACCCAGACTCGAGTGCAGTGGTGTG AGAGT A POLG2 Ensembl:ENSG00000256525 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1482384264 Functional Loss DEL dbSNP153 33..36 33 - - - 40913 RMVar_ID_40913 Human_SNP_ID_630049785 A-to-I Human chr17 - 64500919 64500919 64500919 TTTTCTTTTTTCAACCTCAATGGTATTCCTACAGGAAATGGATAACCATTTTAACTGTATTTTTT TTTTCTTTTTTCAACCTCAATGGTATTCCTACGGGAAATGGATAACCATTTTAACTGTATTTTTT T C DDX5 Ensembl:ENSG00000108654 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs546912689 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_497354,Human_RBP_ID_1369473,Human_RBP_ID_1540152,Human_RBP_ID_1866971,Human_RBP_ID_2519283,Human_RBP_ID_6633479,Human_RBP_ID_13130598,Human_RBP_ID_18706080,Human_RBP_ID_19085439,Human_RBP_ID_20256016,Human_RBP_ID_22806224,Human_RBP_ID_22961486,Human_RBP_ID_23743468,Human_RBP_ID_24480594,Human_RBP_ID_24559387,Human_RBP_ID_25316927,Human_RBP_ID_26645258,Human_RBP_ID_26968848 RMVar_hsa_circ_59606,RMVar_hsa_circ_60060 40914 RMVar_ID_40914 Human_SNP_ID_630050017 A-to-I Human chr17 - 64501798 64501798 64501798 TAGTGATCGGCTGGCTGCTTCCAGTCGATTAGAGAGGTGAAAAAGCTGAACGTGTGCCAGTAATC TAGTGATCGGCTGGCTGCTTCCAGTCGATTAGCGAGGTGAAAAAGCTGAACGTGTGCCAGTAATC T G DDX5 Ensembl:ENSG00000108654 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs781798315 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_497382,Human_RBP_ID_1540152,Human_RBP_ID_1866986,Human_RBP_ID_2519303,Human_RBP_ID_3534223,Human_RBP_ID_8460506,Human_RBP_ID_9887713,Human_RBP_ID_13130607,Human_RBP_ID_18295594,Human_RBP_ID_18706115,Human_RBP_ID_22959645,Human_RBP_ID_23743503,Human_RBP_ID_25346387 RMVar_hsa_circ_59606,RMVar_hsa_circ_60060 40915 RMVar_ID_40915 Human_SNP_ID_630056748 A-to-I Human chr17 + 64521044 64521044 64521044 GGTGGGCGGATCACCTGAGGTAGGAGTTCGAGACCAGCCTGGCCAACATAGTGAAACCCTGTCAC GGTGGGCGGATCACCTGAGGTAGGAGTTCGAGGCCAGCCTGGCCAACATAGTGAAACCCTGTCAC A G CEP95 Ensembl:ENSG00000258890 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1424002840 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_186451,RMVar_hsa_circ_109489,RMVar_hsa_circ_120668,RMVar_hsa_circ_186452,RMVar_hsa_circ_322145,RMVar_hsa_circ_69813,RMVar_hsa_circ_369052,RMVar_hsa_circ_355574,RMVar_hsa_circ_357640,RMVar_hsa_circ_63877,RMVar_hsa_circ_56462,RMVar_hsa_circ_186459,RMVar_hsa_circ_270906,RMVar_hsa_circ_65454,RMVar_hsa_circ_186453,RMVar_hsa_circ_59544,RMVar_hsa_circ_315381,RMVar_hsa_circ_360213,RMVar_hsa_circ_291630,RMVar_hsa_circ_351748,RMVar_hsa_circ_186457,RMVar_hsa_circ_301877,RMVar_hsa_circ_280210,RMVar_hsa_circ_291364,RMVar_hsa_circ_271549,RMVar_hsa_circ_186463,RMVar_hsa_circ_79428,RMVar_hsa_circ_186464,RMVar_hsa_circ_186461,RMVar_hsa_circ_186462,RMVar_hsa_circ_186460,RMVar_hsa_circ_186458 40916 RMVar_ID_40916 Human_SNP_ID_630056753 A-to-I Human chr17 + 64521061 64521061 64521061 AGGTAGGAGTTCGAGACCAGCCTGGCCAACATAGTGAAACCCTGTCACAATACAAAAAATTAGCC AGGTAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCTGTCACAATACAAAAAATTAGCC A G CEP95 Ensembl:ENSG00000258890 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1555677652 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_186451,RMVar_hsa_circ_109489,RMVar_hsa_circ_120668,RMVar_hsa_circ_186452,RMVar_hsa_circ_322145,RMVar_hsa_circ_69813,RMVar_hsa_circ_369052,RMVar_hsa_circ_355574,RMVar_hsa_circ_357640,RMVar_hsa_circ_63877,RMVar_hsa_circ_56462,RMVar_hsa_circ_186459,RMVar_hsa_circ_270906,RMVar_hsa_circ_65454,RMVar_hsa_circ_186453,RMVar_hsa_circ_59544,RMVar_hsa_circ_315381,RMVar_hsa_circ_360213,RMVar_hsa_circ_291630,RMVar_hsa_circ_351748,RMVar_hsa_circ_186457,RMVar_hsa_circ_301877,RMVar_hsa_circ_280210,RMVar_hsa_circ_291364,RMVar_hsa_circ_271549,RMVar_hsa_circ_186463,RMVar_hsa_circ_79428,RMVar_hsa_circ_186464,RMVar_hsa_circ_186461,RMVar_hsa_circ_186462,RMVar_hsa_circ_186460,RMVar_hsa_circ_186458 40917 RMVar_ID_40917 Human_SNP_ID_630057773 A-to-I Human chr17 + 64524860 64524860 64524860 AGGCGCGGTGGCAGGTGCCTGTAATCCCAGCTACTCTGGAGGCTGAGTCAGGAGAATTGCTTGAA AGGCGCGGTGGCAGGTGCCTGTAATCCCAGCTGCTCTGGAGGCTGAGTCAGGAGAATTGCTTGAA A G CEP95 Ensembl:ENSG00000258890 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1213588732 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_186451,RMVar_hsa_circ_109489,RMVar_hsa_circ_120668,RMVar_hsa_circ_186452,RMVar_hsa_circ_69813,RMVar_hsa_circ_355574,RMVar_hsa_circ_63877,RMVar_hsa_circ_56462,RMVar_hsa_circ_186459,RMVar_hsa_circ_65454,RMVar_hsa_circ_59544,RMVar_hsa_circ_360213,RMVar_hsa_circ_291630,RMVar_hsa_circ_351748,RMVar_hsa_circ_186457,RMVar_hsa_circ_301877,RMVar_hsa_circ_280210,RMVar_hsa_circ_291364,RMVar_hsa_circ_271549,RMVar_hsa_circ_186463,RMVar_hsa_circ_79428,RMVar_hsa_circ_186461,RMVar_hsa_circ_186462,RMVar_hsa_circ_186460,RMVar_hsa_circ_25741,RMVar_hsa_circ_72154,RMVar_hsa_circ_327967,RMVar_hsa_circ_186458,RMVar_hsa_circ_343659,RMVar_hsa_circ_50761,RMVar_hsa_circ_310767,RMVar_hsa_circ_186468,RMVar_hsa_circ_21622,RMVar_hsa_circ_360603,RMVar_hsa_circ_335687,RMVar_hsa_circ_56635,RMVar_hsa_circ_288303,RMVar_hsa_circ_186469,RMVar_hsa_circ_186470 40918 RMVar_ID_40918 Human_SNP_ID_630064217 A-to-I Human chr17 - 64548663 64548663 64548663 CAAATGTAGGCCAGGTGTAGTGGCTCACACCTATAATCCTAGCACTTTGGGAGGCTGAGGCAGGC CAAATGTAGGCCAGGTGTAGTGGCTCACACCTGTAATCCTAGCACTTTGGGAGGCTGAGGCAGGC T C SMURF2 Ensembl:ENSG00000108854 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1407051277 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11236,RMVar_hsa_circ_61665,RMVar_hsa_circ_186475,RMVar_hsa_circ_21156,RMVar_hsa_circ_80296,RMVar_hsa_circ_186476,RMVar_hsa_circ_323011,RMVar_hsa_circ_186478 40919 RMVar_ID_40919 Human_SNP_ID_630082481 A-to-I Human chr17 - 64626680 64626680 64626680 CGGCTCACTGCAACCTCTGCCTCTTAGGTTCAAGCGATTCCCTTGCCTCAGCCTCCTGAGTATCT CGGCTCACTGCAACCTCTGCCTCTTAGGTTCAGGCGATTCCCTTGCCTCAGCCTCCTGAGTATCT T C SMURF2 Ensembl:ENSG00000108854 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs545997012 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_186510,RMVar_hsa_circ_113170 40920 RMVar_ID_40920 Human_SNP_ID_630084169 A-to-I Human chr17 - 64633213 64633213 64633213 CAGGATGGAGTACAGTGATATGATCATGGCTCACTGCAGCCTCGGCCTCCTGGGCTCAAGCCATC CAGGATGGAGTACAGTGATATGATCATGGCTCGCTGCAGCCTCGGCCTCCTGGGCTCAAGCCATC T C SMURF2 Ensembl:ENSG00000108854 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474749344 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_186510,RMVar_hsa_circ_113170 40921 RMVar_ID_40921 Human_SNP_ID_630085245 A-to-I Human chr17 - 64637692 64637692 64637692 AGGCATGGTGGCACACGACTGTAGTCTCAGCTACTGGGGAGGCAGAGGTGGGAGAATCGCCTGAA AGGCATGGTGGCACACGACTGTAGTCTCAGCTGCTGGGGAGGCAGAGGTGGGAGAATCGCCTGAA T C SMURF2 Ensembl:ENSG00000108854 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984989641 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6634088,Human_RBP_ID_25317517 RMVar_hsa_circ_186510,RMVar_hsa_circ_113170 40922 RMVar_ID_40922 Human_SNP_ID_630085246 A-to-I Human chr17 - 64637692 64637692 64637692 AGGCATGGTGGCACACGACTGTAGTCTCAGCTACTGGGGAGGCAGAGGTGGGAGAATCGCCTGAA AGGCATGGTGGCACACGACTGTAGTCTCAGCTCCTGGGGAGGCAGAGGTGGGAGAATCGCCTGAA T G SMURF2 Ensembl:ENSG00000108854 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984989641 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6634088,Human_RBP_ID_25317517 RMVar_hsa_circ_186510,RMVar_hsa_circ_113170 40923 RMVar_ID_40923 Human_SNP_ID_630087924 A-to-I Human chr17 - 64648690 64648690 64648690 ATGGCTCACTATAGCCTTGACCACCTGGGCTCAAGTAATCCTCCTGCCTCTGCCTCCTGAGTAGC ATGGCTCACTATAGCCTTGACCACCTGGGCTCGAGTAATCCTCCTGCCTCTGCCTCCTGAGTAGC T C SMURF2 Ensembl:ENSG00000108854 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1357684977 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_186510,RMVar_hsa_circ_113170 40924 RMVar_ID_40924 Human_SNP_ID_630128351 A-to-I Human chr17 - 64816533 64816533 64816533 TAGAGACGGGGTTTTACCATCTTGGCCATGCTAGTCTTGAACTCCTGATCTTGTGGTTCTACTAC TAGAGACGGGGTTTTACCATCTTGGCCATGCTGGTCTTGAACTCCTGATCTTGTGGTTCTACTAC T C PLEKHM1P1 Ensembl:ENSG00000214176 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1445151233 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17379964 RMVar_hsa_circ_21448,RMVar_hsa_circ_186511,RMVar_hsa_circ_102354,RMVar_hsa_circ_318909,RMVar_hsa_circ_335103,RMVar_hsa_circ_95453,RMVar_hsa_circ_186518,RMVar_hsa_circ_361089,RMVar_hsa_circ_186520,RMVar_hsa_circ_324918 40925 RMVar_ID_40925 Human_SNP_ID_630129177 A-to-I Human chr17 - 64820333 64820333 64820333 GTGGTGGCGGGCGCCTGAAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATGGTGTGGACCCG GTGGTGGCGGGCGCCTGAAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGTGTGGACCCG T C PLEKHM1P1 Ensembl:ENSG00000214176 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1394489015 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21448,RMVar_hsa_circ_186511,RMVar_hsa_circ_102354,RMVar_hsa_circ_318909,RMVar_hsa_circ_335103,RMVar_hsa_circ_95453,RMVar_hsa_circ_186518,RMVar_hsa_circ_361089,RMVar_hsa_circ_186520,RMVar_hsa_circ_324918 40926 RMVar_ID_40926 Human_SNP_ID_630162177 A-to-I Human chr17 - 64964506 64964506 64964506 TTGTCCAGGCTGGTCTGGAACTCCTGAGCTCAAGCAATCTGCCTGCCTTGGTCTCCCAAAGTGCT TTGTCCAGGCTGGTCTGGAACTCCTGAGCTCACGCAATCTGCCTGCCTTGGTCTCCCAAAGTGCT T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1196033593 Functional Loss SNV dbSNP153 33..33 33 - - - 40927 RMVar_ID_40927 Human_SNP_ID_630163630 A-to-I Human chr17 - 64971129 64971126 64971129 TCTCCCTCTATCACCCAGGCTGATCATGGGTCACTGCAACCTCAGCCTCCTGGGCTGAAGGGATC TCTCCCTCTATCACCCAGGCTGATCATGGGTC___GCAACCTCAGCCTCCTGGGCTGAAGGGATC CAGT C AMZ2P1 Ensembl:ENSG00000214174 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1391512221 Functional Loss DEL dbSNP153 33..35 33 - - - 40928 RMVar_ID_40928 Human_SNP_ID_630180971 A-to-I Human chr17 - 65043443 65043443 65043443 GCCTCTACAGAATACGCAAAAATTAGTTGAGCATGGTGGCGCACACCTGTGGTCCCAGCTACTCG GCCTCTACAGAATACGCAAAAATTAGTTGAGCGTGGTGGCGCACACCTGTGGTCCCAGCTACTCG T C GNA13 Ensembl:ENSG00000120063 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs951016281 Functional Loss SNV dbSNP153 33..33 33 - - - 40929 RMVar_ID_40929 Human_SNP_ID_630182384 A-to-I Human chr17 - 65049234 65049234 65049234 ATGGTGACATGTACCTGTAGTCCTGGCTACTCAGGAGACTGAGGCACGAGAATCGCTTGAACTCA ATGGTGACATGTACCTGTAGTCCTGGCTACTCGGGAGACTGAGGCACGAGAATCGCTTGAACTCA T C GNA13 Ensembl:ENSG00000120063 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs997589490 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13134606 40930 RMVar_ID_40930 Human_SNP_ID_630182538 A-to-I Human chr17 - 65049958 65049958 65049958 ACATACCCTAATTTTTTGCTTCTATAGCTCTCATCATGCGTAGTCCCTCTGCCAGAATTATTCTT ACATACCCTAATTTTTTGCTTCTATAGCTCTCGTCATGCGTAGTCCCTCTGCCAGAATTATTCTT T C GNA13 Ensembl:ENSG00000120063 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11656396 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_4773,GWAS_ID_4774,GWAS_ID_4775,GWAS_ID_4776,GWAS_ID_4777,GWAS_ID_4778 40931 RMVar_ID_40931 Human_SNP_ID_630183237 A-to-I Human chr17 - 65052883 65052883 65052883 AGCTGGGTCTATAGGCGCGTGCCACCACACCTAGCTAATTTTTGTCTTTTTAGTAGAGGCAGTTT AGCTGGGTCTATAGGCGCGTGCCACCACACCTCGCTAATTTTTGTCTTTTTAGTAGAGGCAGTTT T G GNA13 Ensembl:ENSG00000120063 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs894013588 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13134675 40932 RMVar_ID_40932 Human_SNP_ID_630306313 A-to-I Human chr17 - 65534830 65534830 65534830 CGCCTCCTGGGTTCAGGCAGTTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTGCAGGCGCCCA CGCCTCCTGGGTTCAGGCAGTTCTCCTGCCTCTGCCTCCCGAGTAGCTGGGATTGCAGGCGCCCA T A AXIN2 Ensembl:ENSG00000168646 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs767744784 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265200 40933 RMVar_ID_40933 Human_SNP_ID_630338035 A-to-I Human chr17 - 65655273 65655273 65655273 CTGAGGCTGCGGTCGCTCAGCCTGCACCCAACAAAGGCAGTCTGCACCATAGATCACCGTATTCT CTGAGGCTGCGGTCGCTCAGCCTGCACCCAACGAAGGCAGTCTGCACCATAGATCACCGTATTCT T C CEP112 Ensembl:ENSG00000154240 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1019603658 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_186547,RMVar_hsa_circ_376420,RMVar_hsa_circ_186548 40934 RMVar_ID_40934 Human_SNP_ID_630338036 A-to-I Human chr17 - 65655276 65655276 65655276 TGTCTGAGGCTGCGGTCGCTCAGCCTGCACCCAACAAAGGCAGTCTGCACCATAGATCACCGTAT TGTCTGAGGCTGCGGTCGCTCAGCCTGCACCCGACAAAGGCAGTCTGCACCATAGATCACCGTAT T C CEP112 Ensembl:ENSG00000154240 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965333610 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_186547,RMVar_hsa_circ_376420,RMVar_hsa_circ_186548 40935 RMVar_ID_40935 Human_SNP_ID_630338048 A-to-I Human chr17 - 65655302 65655302 65655302 ATTTTCATCGAGAAATCCAGCTGTAGTGTCTGAGGCTGCGGTCGCTCAGCCTGCACCCAACAAAG ATTTTCATCGAGAAATCCAGCTGTAGTGTCTGGGGCTGCGGTCGCTCAGCCTGCACCCAACAAAG T C CEP112 Ensembl:ENSG00000154240 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878902265 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_186547,RMVar_hsa_circ_376420,RMVar_hsa_circ_186548 40936 RMVar_ID_40936 Human_SNP_ID_630464521 A-to-I Human chr17 - 66197843 66197843 66197843 CATCTTCATCAAAAGGAACTGCAAAACTGTTCAATACATCAAGTACTTTCTTTTGCCATGACCCC CATCTTCATCAAAAGGAACTGCAAAACTGTTCGATACATCAAGTACTTTCTTTTGCCATGACCCC T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1017627696 Functional Loss SNV dbSNP153 33..33 33 - - - 40937 RMVar_ID_40937 Human_SNP_ID_630504184 A-to-I Human chr17 + 66353700 66353700 66353700 ATCGGGCCATTGCACTCCAGCCTGGGCGACAGAGCAAGACTCTTTCTCAAAGAAAGCACCAAAGA ATCGGGCCATTGCACTCCAGCCTGGGCGACAGGGCAAGACTCTTTCTCAAAGAAAGCACCAAAGA A G PRKCA Ensembl:ENSG00000154229 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1323597180 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113290,RMVar_hsa_circ_121666,RMVar_hsa_circ_116079,RMVar_hsa_circ_80677,RMVar_hsa_circ_186581,RMVar_hsa_circ_186582,RMVar_hsa_circ_186580,RMVar_hsa_circ_186584 40938 RMVar_ID_40938 Human_SNP_ID_630551534 A-to-I Human chr17 + 66551248 66551248 66551248 CCACACCTGGCTAATTTTTTATACTTTTCCGTAGAGACAGGGTTTTGCCATGTTGCCTTGGCTTC CCACACCTGGCTAATTTTTTATACTTTTCCGTGGAGACAGGGTTTTGCCATGTTGCCTTGGCTTC A G PRKCA Ensembl:ENSG00000154229 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973067959 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_186588,RMVar_hsa_circ_186589,RMVar_hsa_circ_186590 40939 RMVar_ID_40939 Human_SNP_ID_630586528 A-to-I Human chr17 + 66698940 66698940 66698940 AGGCAGAGATTGCAGTGAGCTGAGATTTTGCCACTGCACTCCAGCCTGGGTGACAGAGCGAGACT AGGCAGAGATTGCAGTGAGCTGAGATTTTGCCGCTGCACTCCAGCCTGGGTGACAGAGCGAGACT A G PRKCA Ensembl:ENSG00000154229 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1316247506 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_354618,RMVar_hsa_circ_104911,RMVar_hsa_circ_90409,RMVar_hsa_circ_186589,RMVar_hsa_circ_186590,RMVar_hsa_circ_186592,RMVar_hsa_circ_356343,RMVar_hsa_circ_361688,RMVar_hsa_circ_117463,RMVar_hsa_circ_186595,RMVar_hsa_circ_100835,RMVar_hsa_circ_121073,RMVar_hsa_circ_355895,RMVar_hsa_circ_186596,RMVar_hsa_circ_111728,RMVar_hsa_circ_186597,RMVar_hsa_circ_186598,RMVar_hsa_circ_102543,RMVar_hsa_circ_186600,RMVar_hsa_circ_366656 40940 RMVar_ID_40940 Human_SNP_ID_630589263 A-to-I Human chr17 + 66710768 66710768 66710768 TAAAATTTTACCTGCTGGGCACGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGC TAAAATTTTACCTGCTGGGCACGGTGGCTCACCCCTGTAATCCCAGCACTTTGGGAGGCCGAGGC A C PRKCA Ensembl:ENSG00000154229 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1178525831 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_354618,RMVar_hsa_circ_104911,RMVar_hsa_circ_90409,RMVar_hsa_circ_186589,RMVar_hsa_circ_186590,RMVar_hsa_circ_186592,RMVar_hsa_circ_356343,RMVar_hsa_circ_361688,RMVar_hsa_circ_117463,RMVar_hsa_circ_186595,RMVar_hsa_circ_100835,RMVar_hsa_circ_121073,RMVar_hsa_circ_355895,RMVar_hsa_circ_186596,RMVar_hsa_circ_111728,RMVar_hsa_circ_186597,RMVar_hsa_circ_186598,RMVar_hsa_circ_102543,RMVar_hsa_circ_186600,RMVar_hsa_circ_366656 40941 RMVar_ID_40941 Human_SNP_ID_630591464 A-to-I Human chr17 + 66719652 66719651 66719652 AGCCAGGCATGGTGACATGTTCCTGTAATCCCAGCTACTCAGGAGGCTGAGGTGCGAGAATCGCT AGCCAGGCATGGTGACATGTTCCTGTAATCCC_GCTACTCAGGAGGCTGAGGTGCGAGAATCGCT CA C PRKCA Ensembl:ENSG00000154229 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1441677560 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_116079,RMVar_hsa_circ_80677,RMVar_hsa_circ_186580,RMVar_hsa_circ_186584,RMVar_hsa_circ_354618,RMVar_hsa_circ_104911,RMVar_hsa_circ_90409,RMVar_hsa_circ_186589,RMVar_hsa_circ_186590,RMVar_hsa_circ_186592,RMVar_hsa_circ_356343,RMVar_hsa_circ_361688,RMVar_hsa_circ_117463,RMVar_hsa_circ_186595,RMVar_hsa_circ_100835,RMVar_hsa_circ_121073,RMVar_hsa_circ_355895,RMVar_hsa_circ_186596,RMVar_hsa_circ_111728,RMVar_hsa_circ_186597,RMVar_hsa_circ_186598,RMVar_hsa_circ_102543,RMVar_hsa_circ_186600,RMVar_hsa_circ_366656 40942 RMVar_ID_40942 Human_SNP_ID_630591466 A-to-I Human chr17 + 66719660 66719660 66719660 ATGGTGACATGTTCCTGTAATCCCAGCTACTCAGGAGGCTGAGGTGCGAGAATCGCTTGAACCCA ATGGTGACATGTTCCTGTAATCCCAGCTACTCGGGAGGCTGAGGTGCGAGAATCGCTTGAACCCA A G PRKCA Ensembl:ENSG00000154229 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs565278913 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_354618,RMVar_hsa_circ_104911,RMVar_hsa_circ_90409,RMVar_hsa_circ_186589,RMVar_hsa_circ_186590,RMVar_hsa_circ_186592,RMVar_hsa_circ_356343,RMVar_hsa_circ_361688,RMVar_hsa_circ_117463,RMVar_hsa_circ_186595,RMVar_hsa_circ_100835,RMVar_hsa_circ_121073,RMVar_hsa_circ_355895,RMVar_hsa_circ_186596,RMVar_hsa_circ_111728,RMVar_hsa_circ_186597,RMVar_hsa_circ_186598,RMVar_hsa_circ_102543,RMVar_hsa_circ_186600,RMVar_hsa_circ_366656 40943 RMVar_ID_40943 Human_SNP_ID_630705056 A-to-I Human chr17 - 67176671 67176671 67176671 TCACCATACCGGCTTCATTTTGTATTTTTTGTAGAGATGGGATTTTGCCATGTTGCCCAGGGAAG TCACCATACCGGCTTCATTTTGTATTTTTTGTGGAGATGGGATTTTGCCATGTTGCCCAGGGAAG T C HELZ Ensembl:ENSG00000198265 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1221771003 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69181,RMVar_hsa_circ_65428,RMVar_hsa_circ_27252,RMVar_hsa_circ_83501,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_47345,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_11025,RMVar_hsa_circ_53144,RMVar_hsa_circ_186643,RMVar_hsa_circ_186647,RMVar_hsa_circ_327881,RMVar_hsa_circ_77333,RMVar_hsa_circ_186650,RMVar_hsa_circ_186648,RMVar_hsa_circ_289232,RMVar_hsa_circ_327869,RMVar_hsa_circ_108539,RMVar_hsa_circ_186652,RMVar_hsa_circ_186653,RMVar_hsa_circ_186651,RMVar_hsa_circ_186661,RMVar_hsa_circ_13630,RMVar_hsa_circ_186656,RMVar_hsa_circ_102321,RMVar_hsa_circ_364254,RMVar_hsa_circ_369054,RMVar_hsa_circ_186657,RMVar_hsa_circ_300757,RMVar_hsa_circ_186658,RMVar_hsa_circ_368210,RMVar_hsa_circ_287233,RMVar_hsa_circ_186663,RMVar_hsa_circ_186659,RMVar_hsa_circ_186660,RMVar_hsa_circ_350195 40944 RMVar_ID_40944 Human_SNP_ID_630709563 A-to-I Human chr17 - 67196127 67196127 67196127 GAACCTCTAGCCGGGCGTGGTGGCTCACGCCTATAATTCTAGCACTTTAGGAGGCCGAGGCGGGC GAACCTCTAGCCGGGCGTGGTGGCTCACGCCTGTAATTCTAGCACTTTAGGAGGCCGAGGCGGGC T C HELZ Ensembl:ENSG00000198265 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 29129909,30559470 RNA-Seq:(High) rs1023580021 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_132271 RMVar_hsa_circ_50307,RMVar_hsa_circ_97056,RMVar_hsa_circ_186635,RMVar_hsa_circ_9579,RMVar_hsa_circ_186650,RMVar_hsa_circ_108539,RMVar_hsa_circ_186658,RMVar_hsa_circ_64027,RMVar_hsa_circ_358737,RMVar_hsa_circ_59150,RMVar_hsa_circ_113998,RMVar_hsa_circ_186666,RMVar_hsa_circ_67945,RMVar_hsa_circ_266525 40945 RMVar_ID_40945 Human_SNP_ID_630709564 A-to-I Human chr17 - 67196127 67196127 67196127 GAACCTCTAGCCGGGCGTGGTGGCTCACGCCTATAATTCTAGCACTTTAGGAGGCCGAGGCGGGC GAACCTCTAGCCGGGCGTGGTGGCTCACGCCTCTAATTCTAGCACTTTAGGAGGCCGAGGCGGGC T G HELZ Ensembl:ENSG00000198265 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 29129909,30559470 RNA-Seq:(High) rs1023580021 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_132271 RMVar_hsa_circ_50307,RMVar_hsa_circ_97056,RMVar_hsa_circ_186635,RMVar_hsa_circ_9579,RMVar_hsa_circ_186650,RMVar_hsa_circ_108539,RMVar_hsa_circ_186658,RMVar_hsa_circ_64027,RMVar_hsa_circ_358737,RMVar_hsa_circ_59150,RMVar_hsa_circ_113998,RMVar_hsa_circ_186666,RMVar_hsa_circ_67945,RMVar_hsa_circ_266525 40946 RMVar_ID_40946 Human_SNP_ID_630714416 A-to-I Human chr17 - 67215487 67215487 67215487 AAAATTAGCTGGGCGTGGCGGCGCATGCCTGTAGTCCCAGCTACCTGGGAGGCTGGGGCAGGAGA AAAATTAGCTGGGCGTGGCGGCGCATGCCTGTGGTCCCAGCTACCTGGGAGGCTGGGGCAGGAGA T C HELZ Ensembl:ENSG00000198265 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1414519894 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50307,RMVar_hsa_circ_97056,RMVar_hsa_circ_186635,RMVar_hsa_circ_186650,RMVar_hsa_circ_108539,RMVar_hsa_circ_64027,RMVar_hsa_circ_59150,RMVar_hsa_circ_113998,RMVar_hsa_circ_186666,RMVar_hsa_circ_67945,RMVar_hsa_circ_53779,RMVar_hsa_circ_351128,RMVar_hsa_circ_186667,RMVar_hsa_circ_41292 40947 RMVar_ID_40947 Human_SNP_ID_630716017 A-to-I Human chr17 - 67221954 67221954 67221954 ATGCACTTGTAGTCCCAGCTTTTTGGGAGGCCAAGGAAGGAGGATGATTCCCAAGTGTGTGGCAG ATGCACTTGTAGTCCCAGCTTTTTGGGAGGCCGAGGAAGGAGGATGATTCCCAAGTGTGTGGCAG T C HELZ Ensembl:ENSG00000198265 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1290760167 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50307,RMVar_hsa_circ_97056,RMVar_hsa_circ_186635,RMVar_hsa_circ_113998,RMVar_hsa_circ_186666,RMVar_hsa_circ_67945,RMVar_hsa_circ_53779 40948 RMVar_ID_40948 Human_SNP_ID_630747401 A-to-I Human chr17 - 67338651 67338651 67338651 GATGGTTTCATCATGTTGGCCGGGCTGGTCTCAAACTCCTGACCTCAGGTGATCCACCCGCCTTG GATGGTTTCATCATGTTGGCCGGGCTGGTCTCCAACTCCTGACCTCAGGTGATCCACCCGCCTTG T G PSMD12 Ensembl:ENSG00000197170 Protein coding 3'UTR GSE38233;GSE100210;GSE99789;GSE112787;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;293 Flip-In T-REx cells,empty vector;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,29796672,29967493,31158229,31158229 RNA-Seq:(High) rs1407661619 Functional Loss SNV dbSNP153 33..33 33 - - - 40949 RMVar_ID_40949 Human_SNP_ID_630747412 A-to-I Human chr17 - 67338712 67338712 67338712 AAGTAGCTGGGATTATAGGCGCCTGCCACCACACCTAGCTAATTTTTGTGTTTTTAGTAGAGATG AAGTAGCTGGGATTATAGGCGCCTGCCACCACGCCTAGCTAATTTTTGTGTTTTTAGTAGAGATG T C PSMD12 Ensembl:ENSG00000197170 Protein coding 3'UTR GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs1022338314 Functional Loss SNV dbSNP153 33..33 33 - - - 40950 RMVar_ID_40950 Human_SNP_ID_630747428 A-to-I Human chr17 - 67338769 67338769 67338769 CGGCTCACTGCAACCTTTGCCTCCCATATTCAAGCAGTTCTCCTGCCTCAACCTCCCAAGTAGCT CGGCTCACTGCAACCTTTGCCTCCCATATTCAGGCAGTTCTCCTGCCTCAACCTCCCAAGTAGCT T C PSMD12 Ensembl:ENSG00000197170 Protein coding 3'UTR GSE100210;GSE99789 HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 29129909,29796672 RNA-Seq:(High) rs565103732 Functional Loss SNV dbSNP153 33..33 33 - - - 40951 RMVar_ID_40951 Human_SNP_ID_630747434 A-to-I Human chr17 - 67338795 67338795 67338795 CAGGCTGGATTGCAGTGTCACGATCTCGGCTCACTGCAACCTTTGCCTCCCATATTCAAGCAGTT CAGGCTGGATTGCAGTGTCACGATCTCGGCTCGCTGCAACCTTTGCCTCCCATATTCAAGCAGTT T C PSMD12 Ensembl:ENSG00000197170 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1469664323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8253640,Human_RBP_ID_18513832,Human_RBP_ID_23171332 40952 RMVar_ID_40952 Human_SNP_ID_630747591 A-to-I Human chr17 - 67339338 67339338 67339338 GGGAGGCCAAGGCGGGTGGATCATCTAAGGTCAGGATTTCGAGACTAGCCTGGCCAACATGGCAA GGGAGGCCAAGGCGGGTGGATCATCTAAGGTCGGGATTTCGAGACTAGCCTGGCCAACATGGCAA T C PSMD12 Ensembl:ENSG00000197170 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569866149 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21927690 40953 RMVar_ID_40953 Human_SNP_ID_630748503 A-to-I Human chr17 - 67342781 67342781 67342781 TAGGCATGCACCACCATATTCAGCTAATTTTTAAATTTTTTGTGGGGATGGGGTCTTGCTGTGTT TAGGCATGCACCACCATATTCAGCTAATTTTTGAATTTTTTGTGGGGATGGGGTCTTGCTGTGTT T C PSMD12 Ensembl:ENSG00000197170 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1312797030 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_186668,RMVar_hsa_circ_89846 40954 RMVar_ID_40954 Human_SNP_ID_630748512 A-to-I Human chr17 - 67342814 67342814 67342814 CTCCCCCCTCAGCTTCCTAGGTAGCTAGGACTATAGGCATGCACCACCATATTCAGCTAATTTTT CTCCCCCCTCAGCTTCCTAGGTAGCTAGGACTGTAGGCATGCACCACCATATTCAGCTAATTTTT T C PSMD12 Ensembl:ENSG00000197170 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1301344510 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_186668,RMVar_hsa_circ_89846 40955 RMVar_ID_40955 Human_SNP_ID_630748538 A-to-I Human chr17 - 67342928 67342928 67342928 AATCTTTTTTTTTTTTTTTTTGAAAGAGAGTCAGTGTAGCTCTGTCATCCAGACTGGAGTACAGT AATCTTTTTTTTTTTTTTTTTGAAAGAGAGTCGGTGTAGCTCTGTCATCCAGACTGGAGTACAGT T C PSMD12 Ensembl:ENSG00000197170 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1169484704 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13141489 RMVar_hsa_circ_186668,RMVar_hsa_circ_89846 40956 RMVar_ID_40956 Human_SNP_ID_630748801 A-to-I Human chr17 - 67343985 67343985 67343985 CAGTACCCTCCCTAGGCCGGGCGTGGTGGCTCACACCTGTGATCCCAGCACTTTGGGAGGCTGAG CAGTACCCTCCCTAGGCCGGGCGTGGTGGCTCCCACCTGTGATCCCAGCACTTTGGGAGGCTGAG T G PSMD12 Ensembl:ENSG00000197170 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1428438291 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22588621 RMVar_hsa_circ_186668,RMVar_hsa_circ_89846 40957 RMVar_ID_40957 Human_SNP_ID_630750138 A-to-I Human chr17 - 67349184 67349184 67349184 AGAAACACCCTCTCTACTAAAAATACAAAATTAGCTGGGCGTGGTGGCGCATGCCTGTAATCCCA AGAAACACCCTCTCTACTAAAAATACAAAATTGGCTGGGCGTGGTGGCGCATGCCTGTAATCCCA T C PSMD12 Ensembl:ENSG00000197170 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1343585041 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269772,RMVar_hsa_circ_300328,RMVar_hsa_circ_26095,RMVar_hsa_circ_61716,RMVar_hsa_circ_186669,RMVar_hsa_circ_355694,RMVar_hsa_circ_316916 40958 RMVar_ID_40958 Human_SNP_ID_630750600 A-to-I Human chr17 - 67351202 67351202 67351202 TATTTTTAGTAGAGACGGGGTTTCACCATGTTAGCCAGGTTGGTCTCGATCTCCTGACCTTGTGA TATTTTTAGTAGAGACGGGGTTTCACCATGTTCGCCAGGTTGGTCTCGATCTCCTGACCTTGTGA T G PSMD12 Ensembl:ENSG00000197170 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs556648579 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13141667 RMVar_hsa_circ_269772,RMVar_hsa_circ_61716,RMVar_hsa_circ_355694,RMVar_hsa_circ_51509 40959 RMVar_ID_40959 Human_SNP_ID_630751452 A-to-I Human chr17 - 67354348 67354348 67354348 TAGAGTGCAGTGGTGCAATCATAGCTCACTGCAGCCTCAATCTCATAGGCTCAAGCAGTCCTCCC TAGAGTGCAGTGGTGCAATCATAGCTCACTGCGGCCTCAATCTCATAGGCTCAAGCAGTCCTCCC T C PSMD12 Ensembl:ENSG00000197170 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs981006947 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269772,RMVar_hsa_circ_61716,RMVar_hsa_circ_355694,RMVar_hsa_circ_51509 40960 RMVar_ID_40960 Human_SNP_ID_630751579 A-to-I Human chr17 - 67354833 67354833 67354833 GGCATGTGCCACCACACCCAGCTAATTTTTGTATTTTCAGTAGAGTCAGGGTTTCACCATGTTGC GGCATGTGCCACCACACCCAGCTAATTTTTGTTTTTTCAGTAGAGTCAGGGTTTCACCATGTTGC T A PSMD12 Ensembl:ENSG00000197170 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs9903680 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269772,RMVar_hsa_circ_61716,RMVar_hsa_circ_355694,RMVar_hsa_circ_51509 40961 RMVar_ID_40961 Human_SNP_ID_630751581 A-to-I Human chr17 - 67354841 67354840 67354841 AGATTACAGGCATGTGCCACCACACCCAGCTAATTTTTGTATTTTCAGTAGAGTCAGGGTTTCAC AGATTACAGGCATGTGCCACCACACCCAGCTA_TTTTTGTATTTTCAGTAGAGTCAGGGTTTCAC AT A PSMD12 Ensembl:ENSG00000197170 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1304835275 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_269772,RMVar_hsa_circ_61716,RMVar_hsa_circ_355694,RMVar_hsa_circ_51509 40962 RMVar_ID_40962 Human_SNP_ID_630751582 A-to-I Human chr17 - 67354842 67354842 67354842 GAGATTACAGGCATGTGCCACCACACCCAGCTAATTTTTGTATTTTCAGTAGAGTCAGGGTTTCA GAGATTACAGGCATGTGCCACCACACCCAGCTGATTTTTGTATTTTCAGTAGAGTCAGGGTTTCA T C PSMD12 Ensembl:ENSG00000197170 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1220851692 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269772,RMVar_hsa_circ_61716,RMVar_hsa_circ_355694,RMVar_hsa_circ_51509 40963 RMVar_ID_40963 Human_SNP_ID_630751722 A-to-I Human chr17 - 67355267 67355258 67355267 GGCAATACTGTGAAACCCTGTCTATACAAAAAATACAAAAATTAGCTGAGTGTAGTGGCAGGCGC GGCAATACTGTGAAACCCTGTCTATACAAAAA_________TTAGCTGAGTGTAGTGGCAGGCGC ATTTTTGTAT A PSMD12 Ensembl:ENSG00000197170 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs938068284 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_18706906 RMVar_hsa_circ_269772,RMVar_hsa_circ_61716,RMVar_hsa_circ_355694,RMVar_hsa_circ_51509 40964 RMVar_ID_40964 Human_SNP_ID_630752606 A-to-I Human chr17 - 67358021 67358021 67358021 CCTGCTCCGGAGGCTGAGGCATGAGAATCGCTAGAACCCGGGAGGTGGAGGTTGCAGTGAGCCGA CCTGCTCCGGAGGCTGAGGCATGAGAATCGCTGGAACCCGGGAGGTGGAGGTTGCAGTGAGCCGA T C PSMD12 Ensembl:ENSG00000197170 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs541769329 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61716 40965 RMVar_ID_40965 Human_SNP_ID_630752710 A-to-I Human chr17 - 67358424 67358424 67358424 AGCTGGGACTACAGGTATGCACCACAATGCCCAGCTAATTTTTGTATTTTTTTGTAGAGACAGGT AGCTGGGACTACAGGTATGCACCACAATGCCCGGCTAATTTTTGTATTTTTTTGTAGAGACAGGT T C PSMD12 Ensembl:ENSG00000197170 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1380093018 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61716 40966 RMVar_ID_40966 Human_SNP_ID_630753831 A-to-I Human chr17 - 67362550 67362550 67362550 TCAAGGAATTCTCCTGCCTCGGCGTCCCCAGTAGCTGGGACTACAGGCGTGCACTACCATGCCTG TCAAGGAATTCTCCTGCCTCGGCGTCCCCAGTGGCTGGGACTACAGGCGTGCACTACCATGCCTG T C PSMD12 Ensembl:ENSG00000197170 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs993862753 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61716 40967 RMVar_ID_40967 Human_SNP_ID_630753832 A-to-I Human chr17 - 67362550 67362550 67362550 TCAAGGAATTCTCCTGCCTCGGCGTCCCCAGTAGCTGGGACTACAGGCGTGCACTACCATGCCTG TCAAGGAATTCTCCTGCCTCGGCGTCCCCAGTCGCTGGGACTACAGGCGTGCACTACCATGCCTG T G PSMD12 Ensembl:ENSG00000197170 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs993862753 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61716 40968 RMVar_ID_40968 Human_SNP_ID_630771383 A-to-I Human chr17 + 67427473 67427473 67427473 TGACCTTGTGATCCTCCTGCCTCGGCCTCCCAAAGTGTTGGTATTACAGGCATGAGCCACTGCAC TGACCTTGTGATCCTCCTGCCTCGGCCTCCCAGAGTGTTGGTATTACAGGCATGAGCCACTGCAC A G PITPNC1 Ensembl:ENSG00000154217 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1342135304 Functional Loss SNV dbSNP153 33..33 33 - - - 40969 RMVar_ID_40969 Human_SNP_ID_630774874 A-to-I Human chr17 + 67440756 67440756 67440756 TTTATAGGGATAGGGGTCTTGCCATGTTACCCAGGCTGGTCTCTTAACTCCTGGGCTCAAGAAAT TTTATAGGGATAGGGGTCTTGCCATGTTACCCGGGCTGGTCTCTTAACTCCTGGGCTCAAGAAAT A G PITPNC1 Ensembl:ENSG00000154217 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs768088376 Functional Loss SNV dbSNP153 33..33 33 - - - 40970 RMVar_ID_40970 Human_SNP_ID_630799157 A-to-I Human chr17 + 67537715 67537715 67537715 AGAACTGGTGCTGGGTGCAGTGGCTCACCTCTATAATCCTAGTTCTTTGGGAGGTCGAGGTGGGC AGAACTGGTGCTGGGTGCAGTGGCTCACCTCTGTAATCCTAGTTCTTTGGGAGGTCGAGGTGGGC A G PITPNC1 Ensembl:ENSG00000154217 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1399928187 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_65930,RMVar_hsa_circ_298375,RMVar_hsa_circ_298766,RMVar_hsa_circ_118075,RMVar_hsa_circ_186670,RMVar_hsa_circ_186671,RMVar_hsa_circ_186672 40971 RMVar_ID_40971 Human_SNP_ID_630812289 A-to-I Human chr17 + 67593619 67593619 67593619 CGAGGTTTCACCGTGTTGGCCAGGCTGGTCTCAAACTCCTGGGCTCAAGCAATCTGCCCTCCTTG CGAGGTTTCACCGTGTTGGCCAGGCTGGTCTCGAACTCCTGGGCTCAAGCAATCTGCCCTCCTTG A G PITPNC1 Ensembl:ENSG00000154217 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs929972235 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_65930,RMVar_hsa_circ_298766,RMVar_hsa_circ_186672,RMVar_hsa_circ_48900,RMVar_hsa_circ_126965,RMVar_hsa_circ_186673,RMVar_hsa_circ_186674 40972 RMVar_ID_40972 Human_SNP_ID_630833204 A-to-I Human chr17 + 67682140 67682140 67682140 GGAGAATCGCTTGAACCTGGGAGGCAGAGGTTACAGTGAGCCGAGATGGCGCCACTGCACTCCAG GGAGAATCGCTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCCGAGATGGCGCCACTGCACTCCAG A G PITPNC1 Ensembl:ENSG00000154217 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1456793571 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126965,RMVar_hsa_circ_186674 40973 RMVar_ID_40973 Human_SNP_ID_630833205 A-to-I Human chr17 + 67682140 67682140 67682140 GGAGAATCGCTTGAACCTGGGAGGCAGAGGTTACAGTGAGCCGAGATGGCGCCACTGCACTCCAG GGAGAATCGCTTGAACCTGGGAGGCAGAGGTTTCAGTGAGCCGAGATGGCGCCACTGCACTCCAG A T PITPNC1 Ensembl:ENSG00000154217 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1456793571 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126965,RMVar_hsa_circ_186674 40974 RMVar_ID_40974 Human_SNP_ID_630842246 A-to-I Human chr17 + 67719221 67719220 67719221 AGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAATCCTGTCTCTGCTAAAAATACAAAAATTAG AGGAGTTCGAGACCAGCCTGGCCAACATGGTG_AATCCTGTCTCTGCTAAAAATACAAAAATTAG GA G NOL11 Ensembl:ENSG00000130935 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs550430860 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_21713 40975 RMVar_ID_40975 Human_SNP_ID_630844733 A-to-I Human chr17 + 67727992 67727992 67727992 TATAACTATACCATGTGCGAGCCGGGCACAGTAGCTCATGCCTGTAATCCCAGCACTTTGGGAGG TATAACTATACCATGTGCGAGCCGGGCACAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGG A G NOL11 Ensembl:ENSG00000130935 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1300191268 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13143702 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 40976 RMVar_ID_40976 Human_SNP_ID_630847896 A-to-I Human chr17 + 67740160 67740160 67740160 GGGAGGCTGAGGCAGGAGAACTGTTTGAACCCAGGAGGCGGACGTTGCAGTGAGCTGAGATCGCG GGGAGGCTGAGGCAGGAGAACTGTTTGAACCCCGGAGGCGGACGTTGCAGTGAGCTGAGATCGCG A C NOL11 Ensembl:ENSG00000130935 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs916455121 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88636,RMVar_hsa_circ_186681,RMVar_hsa_circ_109158,RMVar_hsa_circ_186684,RMVar_hsa_circ_23716,RMVar_hsa_circ_378839,RMVar_hsa_circ_63456,RMVar_hsa_circ_65313,RMVar_hsa_circ_120805,RMVar_hsa_circ_186687 40977 RMVar_ID_40977 Human_SNP_ID_630848587 A-to-I Human chr17 + 67743103 67743103 67743103 TCTCTACAAAAATTGCTAAAAAGTAGCTGGGTATGATGGTGCATCTGTAATCCCAGCAACTCTGG TCTCTACAAAAATTGCTAAAAAGTAGCTGGGTGTGATGGTGCATCTGTAATCCCAGCAACTCTGG A G NOL11 Ensembl:ENSG00000130935 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1001371064 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18707025 RMVar_hsa_circ_88636,RMVar_hsa_circ_186681,RMVar_hsa_circ_109158,RMVar_hsa_circ_186684,RMVar_hsa_circ_23716,RMVar_hsa_circ_378839,RMVar_hsa_circ_63456,RMVar_hsa_circ_65313,RMVar_hsa_circ_120805,RMVar_hsa_circ_186687 40978 RMVar_ID_40978 Human_SNP_ID_630853785 A-to-I Human chr17 + 67762985 67762985 67762985 AAAATTAGCTGAGCATGGTGGCGCGCACCTGTAGTCCCAGTTACTCAGAAGGCTGAGACAGGAGA AAAATTAGCTGAGCATGGTGGCGCGCACCTGTCGTCCCAGTTACTCAGAAGGCTGAGACAGGAGA A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1035676226 Functional Loss SNV dbSNP153 33..33 33 - - - 40979 RMVar_ID_40979 Human_SNP_ID_630872317 A-to-I Human chr17 - 67834559 67834559 67834559 AATACATGAATATAAAGCCTCAAAATACATGAAGATTGCTAGAACTTCAAGGAGAAACAGACAAA AATACATGAATATAAAGCCTCAAAATACATGACGATTGCTAGAACTTCAAGGAGAAACAGACAAA T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251003084 Functional Loss SNV dbSNP153 33..33 33 - - - 40980 RMVar_ID_40980 Human_SNP_ID_630875545 A-to-I Human chr17 + 67846728 67846728 67846728 ACTTGTGTGGGTTTGTTTGTTTGTTTGGAGACAGGGTCCCTGTCGCCTAGGGTGGAGTGCGGTGG ACTTGTGTGGGTTTGTTTGTTTGTTTGGAGACTGGGTCCCTGTCGCCTAGGGTGGAGTGCGGTGG A T BPTF Ensembl:ENSG00000171634 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991764575 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13144516 40981 RMVar_ID_40981 Human_SNP_ID_630876391 A-to-I Human chr17 + 67850427 67850427 67850427 CAGAGTCTCGCTCTGTTGCCTAGGCTGGCAGTAGCATGATCTCGGCTCACTGCAACCTCCGTCTC CAGAGTCTCGCTCTGTTGCCTAGGCTGGCAGTGGCATGATCTCGGCTCACTGCAACCTCCGTCTC A G BPTF Ensembl:ENSG00000171634 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1464937952 Functional Loss SNV dbSNP153 33..33 33 - - - 40982 RMVar_ID_40982 Human_SNP_ID_630882958 A-to-I Human chr17 + 67876695 67876695 67876695 GGACATGATATCATGCGCCTGTAATCCCAGCTACTTGGGTGGCTGAGGCAGGAGGATCACTTGAA GGACATGATATCATGCGCCTGTAATCCCAGCTTCTTGGGTGGCTGAGGCAGGAGGATCACTTGAA A T BPTF Ensembl:ENSG00000171634 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1231439466 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74181,RMVar_hsa_circ_105707,RMVar_hsa_circ_340934,RMVar_hsa_circ_115820,RMVar_hsa_circ_112988,RMVar_hsa_circ_96942,RMVar_hsa_circ_97433,RMVar_hsa_circ_24363,RMVar_hsa_circ_104065,RMVar_hsa_circ_186692,RMVar_hsa_circ_186694,RMVar_hsa_circ_56041,RMVar_hsa_circ_186695,RMVar_hsa_circ_186693,RMVar_hsa_circ_186691,RMVar_hsa_circ_307045,RMVar_hsa_circ_101267,RMVar_hsa_circ_186697,RMVar_hsa_circ_186699,RMVar_hsa_circ_186698,RMVar_hsa_circ_283088,RMVar_hsa_circ_41049,RMVar_hsa_circ_55441,RMVar_hsa_circ_105974,RMVar_hsa_circ_186702,RMVar_hsa_circ_76313,RMVar_hsa_circ_186703,RMVar_hsa_circ_186704 40983 RMVar_ID_40983 Human_SNP_ID_630884227 A-to-I Human chr17 + 67881684 67881684 67881684 CGCCACCACATCTGGCTAATTTTTGTATTTATAGTAGAGATGGGGTTTCACATGTTGGCCAGGCT CGCCACCACATCTGGCTAATTTTTGTATTTATGGTAGAGATGGGGTTTCACATGTTGGCCAGGCT A G BPTF Ensembl:ENSG00000171634 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1284380470 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74181,RMVar_hsa_circ_105707,RMVar_hsa_circ_340934,RMVar_hsa_circ_115820,RMVar_hsa_circ_112988,RMVar_hsa_circ_96942,RMVar_hsa_circ_97433,RMVar_hsa_circ_24363,RMVar_hsa_circ_104065,RMVar_hsa_circ_186692,RMVar_hsa_circ_186694,RMVar_hsa_circ_56041,RMVar_hsa_circ_186695,RMVar_hsa_circ_186693,RMVar_hsa_circ_186691,RMVar_hsa_circ_307045,RMVar_hsa_circ_101267,RMVar_hsa_circ_186697,RMVar_hsa_circ_186699,RMVar_hsa_circ_186698,RMVar_hsa_circ_283088,RMVar_hsa_circ_41049,RMVar_hsa_circ_55441,RMVar_hsa_circ_105974,RMVar_hsa_circ_186702,RMVar_hsa_circ_76313,RMVar_hsa_circ_186703,RMVar_hsa_circ_186704 40984 RMVar_ID_40984 Human_SNP_ID_630884658 A-to-I Human chr17 + 67883058 67883058 67883058 GAAAAAAGGGCTGGGCTTGGTGGCTCACGCCTATAATCCCAGCGCTTTGGGAGGCCCAGGTGGGC GAAAAAAGGGCTGGGCTTGGTGGCTCACGCCTGTAATCCCAGCGCTTTGGGAGGCCCAGGTGGGC A G BPTF Ensembl:ENSG00000171634 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277807182 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25346785 RMVar_hsa_circ_74181,RMVar_hsa_circ_105707,RMVar_hsa_circ_340934,RMVar_hsa_circ_115820,RMVar_hsa_circ_112988,RMVar_hsa_circ_96942,RMVar_hsa_circ_97433,RMVar_hsa_circ_24363,RMVar_hsa_circ_104065,RMVar_hsa_circ_186692,RMVar_hsa_circ_186694,RMVar_hsa_circ_56041,RMVar_hsa_circ_186695,RMVar_hsa_circ_186693,RMVar_hsa_circ_186691,RMVar_hsa_circ_307045,RMVar_hsa_circ_101267,RMVar_hsa_circ_186697,RMVar_hsa_circ_186699,RMVar_hsa_circ_186698,RMVar_hsa_circ_283088,RMVar_hsa_circ_41049,RMVar_hsa_circ_55441,RMVar_hsa_circ_105974,RMVar_hsa_circ_186702,RMVar_hsa_circ_76313,RMVar_hsa_circ_186703,RMVar_hsa_circ_186704 40985 RMVar_ID_40985 Human_SNP_ID_630884824 A-to-I Human chr17 + 67883704 67883704 67883704 TCACAGCAACCTCCGCCCCCCTGGGTTCAAGCAGTTCTTCTGCCTCAGCCTCCCAGGTAGCTGGG TCACAGCAACCTCCGCCCCCCTGGGTTCAAGCTGTTCTTCTGCCTCAGCCTCCCAGGTAGCTGGG A T BPTF Ensembl:ENSG00000171634 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs537850914 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74181,RMVar_hsa_circ_105707,RMVar_hsa_circ_340934,RMVar_hsa_circ_115820,RMVar_hsa_circ_112988,RMVar_hsa_circ_96942,RMVar_hsa_circ_97433,RMVar_hsa_circ_24363,RMVar_hsa_circ_104065,RMVar_hsa_circ_186692,RMVar_hsa_circ_186694,RMVar_hsa_circ_56041,RMVar_hsa_circ_186695,RMVar_hsa_circ_186693,RMVar_hsa_circ_186691,RMVar_hsa_circ_307045,RMVar_hsa_circ_101267,RMVar_hsa_circ_186697,RMVar_hsa_circ_186699,RMVar_hsa_circ_186698,RMVar_hsa_circ_283088,RMVar_hsa_circ_41049,RMVar_hsa_circ_55441,RMVar_hsa_circ_105974,RMVar_hsa_circ_186702,RMVar_hsa_circ_76313,RMVar_hsa_circ_186703,RMVar_hsa_circ_186704 40986 RMVar_ID_40986 Human_SNP_ID_630885080 A-to-I Human chr17 + 67884516 67884516 67884516 CGGCTCACTGCAGCCTCTGGCTCTTGGGTTCAAATGATCTTCCTGCCTCAGCCCCTCAAGTACGT CGGCTCACTGCAGCCTCTGGCTCTTGGGTTCAGATGATCTTCCTGCCTCAGCCCCTCAAGTACGT A G BPTF Ensembl:ENSG00000171634 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs907940916 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13145225 RMVar_hsa_circ_74181,RMVar_hsa_circ_105707,RMVar_hsa_circ_340934,RMVar_hsa_circ_115820,RMVar_hsa_circ_112988,RMVar_hsa_circ_96942,RMVar_hsa_circ_97433,RMVar_hsa_circ_24363,RMVar_hsa_circ_104065,RMVar_hsa_circ_186692,RMVar_hsa_circ_186694,RMVar_hsa_circ_56041,RMVar_hsa_circ_186695,RMVar_hsa_circ_186693,RMVar_hsa_circ_186691,RMVar_hsa_circ_307045,RMVar_hsa_circ_101267,RMVar_hsa_circ_186697,RMVar_hsa_circ_186699,RMVar_hsa_circ_186698,RMVar_hsa_circ_283088,RMVar_hsa_circ_41049,RMVar_hsa_circ_55441,RMVar_hsa_circ_105974,RMVar_hsa_circ_186702,RMVar_hsa_circ_76313,RMVar_hsa_circ_186703,RMVar_hsa_circ_186704 40987 RMVar_ID_40987 Human_SNP_ID_630885102 A-to-I Human chr17 + 67884613 67884613 67884613 AATTTTTGTATTTTTCGTAGTGATGGAGTTTCACCGTGTTGCCCAGGCTGGTCTCGAACCCCTGA AATTTTTGTATTTTTCGTAGTGATGGAGTTTCGCCGTGTTGCCCAGGCTGGTCTCGAACCCCTGA A G BPTF Ensembl:ENSG00000171634 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs868615112 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_766117,Human_RBP_ID_13145234 RMVar_hsa_circ_74181,RMVar_hsa_circ_105707,RMVar_hsa_circ_340934,RMVar_hsa_circ_115820,RMVar_hsa_circ_112988,RMVar_hsa_circ_96942,RMVar_hsa_circ_97433,RMVar_hsa_circ_24363,RMVar_hsa_circ_104065,RMVar_hsa_circ_186692,RMVar_hsa_circ_186694,RMVar_hsa_circ_56041,RMVar_hsa_circ_186695,RMVar_hsa_circ_186693,RMVar_hsa_circ_186691,RMVar_hsa_circ_307045,RMVar_hsa_circ_101267,RMVar_hsa_circ_186697,RMVar_hsa_circ_186699,RMVar_hsa_circ_186698,RMVar_hsa_circ_283088,RMVar_hsa_circ_41049,RMVar_hsa_circ_55441,RMVar_hsa_circ_105974,RMVar_hsa_circ_186702,RMVar_hsa_circ_76313,RMVar_hsa_circ_186703,RMVar_hsa_circ_186704 40988 RMVar_ID_40988 Human_SNP_ID_630885303 A-to-I Human chr17 + 67885447 67885447 67885447 CTCTACCAAAAATATAAAAGAATTATCCAGGTATGGTGGCGTGCACCTGACTGTAGTCCCAGCTA CTCTACCAAAAATATAAAAGAATTATCCAGGTGTGGTGGCGTGCACCTGACTGTAGTCCCAGCTA A G BPTF Ensembl:ENSG00000171634 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1248069153 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13145275 RMVar_hsa_circ_74181,RMVar_hsa_circ_105707,RMVar_hsa_circ_340934,RMVar_hsa_circ_115820,RMVar_hsa_circ_112988,RMVar_hsa_circ_96942,RMVar_hsa_circ_97433,RMVar_hsa_circ_24363,RMVar_hsa_circ_104065,RMVar_hsa_circ_186692,RMVar_hsa_circ_186694,RMVar_hsa_circ_56041,RMVar_hsa_circ_186695,RMVar_hsa_circ_186693,RMVar_hsa_circ_186691,RMVar_hsa_circ_307045,RMVar_hsa_circ_101267,RMVar_hsa_circ_186697,RMVar_hsa_circ_186699,RMVar_hsa_circ_186698,RMVar_hsa_circ_283088,RMVar_hsa_circ_41049,RMVar_hsa_circ_55441,RMVar_hsa_circ_105974,RMVar_hsa_circ_186702,RMVar_hsa_circ_76313,RMVar_hsa_circ_186703,RMVar_hsa_circ_186704 40989 RMVar_ID_40989 Human_SNP_ID_630885311 A-to-I Human chr17 + 67885469 67885469 67885469 TTATCCAGGTATGGTGGCGTGCACCTGACTGTAGTCCCAGCTACTCAGGAGGCTGAGGCGGGAGA TTATCCAGGTATGGTGGCGTGCACCTGACTGTGGTCCCAGCTACTCAGGAGGCTGAGGCGGGAGA A G BPTF Ensembl:ENSG00000171634 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1465450272 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13145276 RMVar_hsa_circ_74181,RMVar_hsa_circ_105707,RMVar_hsa_circ_340934,RMVar_hsa_circ_115820,RMVar_hsa_circ_112988,RMVar_hsa_circ_96942,RMVar_hsa_circ_97433,RMVar_hsa_circ_24363,RMVar_hsa_circ_104065,RMVar_hsa_circ_186692,RMVar_hsa_circ_186694,RMVar_hsa_circ_56041,RMVar_hsa_circ_186695,RMVar_hsa_circ_186693,RMVar_hsa_circ_186691,RMVar_hsa_circ_307045,RMVar_hsa_circ_101267,RMVar_hsa_circ_186697,RMVar_hsa_circ_186699,RMVar_hsa_circ_186698,RMVar_hsa_circ_283088,RMVar_hsa_circ_41049,RMVar_hsa_circ_55441,RMVar_hsa_circ_105974,RMVar_hsa_circ_186702,RMVar_hsa_circ_76313,RMVar_hsa_circ_186703,RMVar_hsa_circ_186704 40990 RMVar_ID_40990 Human_SNP_ID_630885312 A-to-I Human chr17 + 67885475 67885472 67885475 AGGTATGGTGGCGTGCACCTGACTGTAGTCCCAGCTACTCAGGAGGCTGAGGCGGGAGAATCTCT AGGTATGGTGGCGTGCACCTGACTGTAGTC___GCTACTCAGGAGGCTGAGGCGGGAGAATCTCT CCCA C BPTF Ensembl:ENSG00000171634 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1303383968 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_13145276 RMVar_hsa_circ_74181,RMVar_hsa_circ_105707,RMVar_hsa_circ_340934,RMVar_hsa_circ_115820,RMVar_hsa_circ_112988,RMVar_hsa_circ_96942,RMVar_hsa_circ_97433,RMVar_hsa_circ_24363,RMVar_hsa_circ_104065,RMVar_hsa_circ_186692,RMVar_hsa_circ_186694,RMVar_hsa_circ_56041,RMVar_hsa_circ_186695,RMVar_hsa_circ_186693,RMVar_hsa_circ_186691,RMVar_hsa_circ_307045,RMVar_hsa_circ_101267,RMVar_hsa_circ_186697,RMVar_hsa_circ_186699,RMVar_hsa_circ_186698,RMVar_hsa_circ_283088,RMVar_hsa_circ_41049,RMVar_hsa_circ_55441,RMVar_hsa_circ_105974,RMVar_hsa_circ_186702,RMVar_hsa_circ_76313,RMVar_hsa_circ_186703,RMVar_hsa_circ_186704 40991 RMVar_ID_40991 Human_SNP_ID_630885314 A-to-I Human chr17 + 67885475 67885475 67885475 AGGTATGGTGGCGTGCACCTGACTGTAGTCCCAGCTACTCAGGAGGCTGAGGCGGGAGAATCTCT AGGTATGGTGGCGTGCACCTGACTGTAGTCCCGGCTACTCAGGAGGCTGAGGCGGGAGAATCTCT A G BPTF Ensembl:ENSG00000171634 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs974991338 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13145276 RMVar_hsa_circ_74181,RMVar_hsa_circ_105707,RMVar_hsa_circ_340934,RMVar_hsa_circ_115820,RMVar_hsa_circ_112988,RMVar_hsa_circ_96942,RMVar_hsa_circ_97433,RMVar_hsa_circ_24363,RMVar_hsa_circ_104065,RMVar_hsa_circ_186692,RMVar_hsa_circ_186694,RMVar_hsa_circ_56041,RMVar_hsa_circ_186695,RMVar_hsa_circ_186693,RMVar_hsa_circ_186691,RMVar_hsa_circ_307045,RMVar_hsa_circ_101267,RMVar_hsa_circ_186697,RMVar_hsa_circ_186699,RMVar_hsa_circ_186698,RMVar_hsa_circ_283088,RMVar_hsa_circ_41049,RMVar_hsa_circ_55441,RMVar_hsa_circ_105974,RMVar_hsa_circ_186702,RMVar_hsa_circ_76313,RMVar_hsa_circ_186703,RMVar_hsa_circ_186704 40992 RMVar_ID_40992 Human_SNP_ID_630887512 A-to-I Human chr17 + 67894392 67894392 67894392 GCACTGTTGCCCAGGCTAGCATGCAGTGGTGTAGTCTCGGCTTGCTGTAACCTCTGCCTCCCATA GCACTGTTGCCCAGGCTAGCATGCAGTGGTGTGGTCTCGGCTTGCTGTAACCTCTGCCTCCCATA A G BPTF Ensembl:ENSG00000171634 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs531112887 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74181,RMVar_hsa_circ_105707,RMVar_hsa_circ_115820,RMVar_hsa_circ_112988,RMVar_hsa_circ_96942,RMVar_hsa_circ_97433,RMVar_hsa_circ_104065,RMVar_hsa_circ_186692,RMVar_hsa_circ_186694,RMVar_hsa_circ_186695,RMVar_hsa_circ_186693,RMVar_hsa_circ_186691,RMVar_hsa_circ_101267,RMVar_hsa_circ_186697,RMVar_hsa_circ_186698,RMVar_hsa_circ_41049,RMVar_hsa_circ_298433,RMVar_hsa_circ_55441,RMVar_hsa_circ_105974,RMVar_hsa_circ_76313,RMVar_hsa_circ_186703,RMVar_hsa_circ_186704,RMVar_hsa_circ_334229,RMVar_hsa_circ_335864,RMVar_hsa_circ_364763,RMVar_hsa_circ_318138,RMVar_hsa_circ_270983,RMVar_hsa_circ_284543,RMVar_hsa_circ_291983,RMVar_hsa_circ_42694,RMVar_hsa_circ_77993,RMVar_hsa_circ_39489,RMVar_hsa_circ_50642,RMVar_hsa_circ_186705,RMVar_hsa_circ_186709,RMVar_hsa_circ_186711,RMVar_hsa_circ_30380,RMVar_hsa_circ_186710,RMVar_hsa_circ_186707,RMVar_hsa_circ_186708,RMVar_hsa_circ_186706,RMVar_hsa_circ_309665,RMVar_hsa_circ_348399,RMVar_hsa_circ_362667,RMVar_hsa_circ_186713,RMVar_hsa_circ_355492,RMVar_hsa_circ_324311,RMVar_hsa_circ_305218,RMVar_hsa_circ_286497,RMVar_hsa_circ_64813,RMVar_hsa_circ_67636,RMVar_hsa_circ_58551,RMVar_hsa_circ_186714,RMVar_hsa_circ_186716,RMVar_hsa_circ_186718,RMVar_hsa_circ_46250,RMVar_hsa_circ_186717,RMVar_hsa_circ_186715,RMVar_hsa_circ_112902,RMVar_hsa_circ_113175,RMVar_hsa_circ_77308,RMVar_hsa_circ_118894,RMVar_hsa_circ_186721,RMVar_hsa_circ_186722,RMVar_hsa_circ_186723,RMVar_hsa_circ_186724,RMVar_hsa_circ_56273,RMVar_hsa_circ_95566,RMVar_hsa_circ_186725 40993 RMVar_ID_40993 Human_SNP_ID_630887528 A-to-I Human chr17 + 67894428 67894428 67894428 TCGGCTTGCTGTAACCTCTGCCTCCCATATTCAAGCGATTCTCTTGTTTCAGCCTCCCAAGTAGC TCGGCTTGCTGTAACCTCTGCCTCCCATATTCCAGCGATTCTCTTGTTTCAGCCTCCCAAGTAGC A C BPTF Ensembl:ENSG00000171634 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1234270046 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74181,RMVar_hsa_circ_105707,RMVar_hsa_circ_115820,RMVar_hsa_circ_112988,RMVar_hsa_circ_96942,RMVar_hsa_circ_97433,RMVar_hsa_circ_104065,RMVar_hsa_circ_186692,RMVar_hsa_circ_186694,RMVar_hsa_circ_186695,RMVar_hsa_circ_186693,RMVar_hsa_circ_186691,RMVar_hsa_circ_101267,RMVar_hsa_circ_186697,RMVar_hsa_circ_186698,RMVar_hsa_circ_41049,RMVar_hsa_circ_298433,RMVar_hsa_circ_55441,RMVar_hsa_circ_105974,RMVar_hsa_circ_76313,RMVar_hsa_circ_186703,RMVar_hsa_circ_186704,RMVar_hsa_circ_334229,RMVar_hsa_circ_335864,RMVar_hsa_circ_364763,RMVar_hsa_circ_318138,RMVar_hsa_circ_270983,RMVar_hsa_circ_284543,RMVar_hsa_circ_291983,RMVar_hsa_circ_42694,RMVar_hsa_circ_77993,RMVar_hsa_circ_39489,RMVar_hsa_circ_50642,RMVar_hsa_circ_186705,RMVar_hsa_circ_186709,RMVar_hsa_circ_186711,RMVar_hsa_circ_30380,RMVar_hsa_circ_186710,RMVar_hsa_circ_186707,RMVar_hsa_circ_186708,RMVar_hsa_circ_186706,RMVar_hsa_circ_309665,RMVar_hsa_circ_348399,RMVar_hsa_circ_362667,RMVar_hsa_circ_186713,RMVar_hsa_circ_355492,RMVar_hsa_circ_324311,RMVar_hsa_circ_305218,RMVar_hsa_circ_286497,RMVar_hsa_circ_64813,RMVar_hsa_circ_67636,RMVar_hsa_circ_58551,RMVar_hsa_circ_186714,RMVar_hsa_circ_186716,RMVar_hsa_circ_186718,RMVar_hsa_circ_46250,RMVar_hsa_circ_186717,RMVar_hsa_circ_186715,RMVar_hsa_circ_112902,RMVar_hsa_circ_113175,RMVar_hsa_circ_77308,RMVar_hsa_circ_118894,RMVar_hsa_circ_186721,RMVar_hsa_circ_186722,RMVar_hsa_circ_186723,RMVar_hsa_circ_186724,RMVar_hsa_circ_56273,RMVar_hsa_circ_95566,RMVar_hsa_circ_186725 40994 RMVar_ID_40994 Human_SNP_ID_630888674 A-to-I Human chr17 + 67898241 67898241 67898241 AAAATTAGCCAGGCATGGTGTTGCATGCCTTTAGTCCCAGCTACTAGGAGGCTGAGGCAGGAGAA AAAATTAGCCAGGCATGGTGTTGCATGCCTTTTGTCCCAGCTACTAGGAGGCTGAGGCAGGAGAA A T BPTF Ensembl:ENSG00000171634 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs113765616 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74181,RMVar_hsa_circ_105707,RMVar_hsa_circ_115820,RMVar_hsa_circ_112988,RMVar_hsa_circ_96942,RMVar_hsa_circ_97433,RMVar_hsa_circ_104065,RMVar_hsa_circ_186692,RMVar_hsa_circ_186694,RMVar_hsa_circ_186695,RMVar_hsa_circ_186693,RMVar_hsa_circ_186691,RMVar_hsa_circ_101267,RMVar_hsa_circ_186697,RMVar_hsa_circ_186698,RMVar_hsa_circ_41049,RMVar_hsa_circ_298433,RMVar_hsa_circ_55441,RMVar_hsa_circ_105974,RMVar_hsa_circ_76313,RMVar_hsa_circ_186703,RMVar_hsa_circ_186704,RMVar_hsa_circ_334229,RMVar_hsa_circ_335864,RMVar_hsa_circ_364763,RMVar_hsa_circ_318138,RMVar_hsa_circ_270983,RMVar_hsa_circ_284543,RMVar_hsa_circ_291983,RMVar_hsa_circ_42694,RMVar_hsa_circ_77993,RMVar_hsa_circ_39489,RMVar_hsa_circ_50642,RMVar_hsa_circ_186705,RMVar_hsa_circ_186709,RMVar_hsa_circ_186711,RMVar_hsa_circ_30380,RMVar_hsa_circ_186710,RMVar_hsa_circ_186707,RMVar_hsa_circ_186708,RMVar_hsa_circ_186706,RMVar_hsa_circ_309665,RMVar_hsa_circ_348399,RMVar_hsa_circ_362667,RMVar_hsa_circ_186713,RMVar_hsa_circ_355492,RMVar_hsa_circ_324311,RMVar_hsa_circ_305218,RMVar_hsa_circ_286497,RMVar_hsa_circ_64813,RMVar_hsa_circ_67636,RMVar_hsa_circ_58551,RMVar_hsa_circ_186714,RMVar_hsa_circ_186716,RMVar_hsa_circ_186718,RMVar_hsa_circ_46250,RMVar_hsa_circ_186717,RMVar_hsa_circ_186715,RMVar_hsa_circ_112902,RMVar_hsa_circ_113175,RMVar_hsa_circ_77308,RMVar_hsa_circ_118894,RMVar_hsa_circ_186721,RMVar_hsa_circ_186722,RMVar_hsa_circ_186723,RMVar_hsa_circ_186724,RMVar_hsa_circ_56273,RMVar_hsa_circ_95566,RMVar_hsa_circ_186725 40995 RMVar_ID_40995 Human_SNP_ID_630888689 A-to-I Human chr17 + 67898302 67898302 67898302 AGAACCACTTGAACCTGGGAGGCAGAGGTTGCAATGAGCTGAGATCGCACCAGTGCACTCCATCC AGAACCACTTGAACCTGGGAGGCAGAGGTTGCCATGAGCTGAGATCGCACCAGTGCACTCCATCC A C BPTF Ensembl:ENSG00000171634 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1568009108 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74181,RMVar_hsa_circ_105707,RMVar_hsa_circ_115820,RMVar_hsa_circ_112988,RMVar_hsa_circ_96942,RMVar_hsa_circ_97433,RMVar_hsa_circ_104065,RMVar_hsa_circ_186692,RMVar_hsa_circ_186694,RMVar_hsa_circ_186695,RMVar_hsa_circ_186693,RMVar_hsa_circ_186691,RMVar_hsa_circ_101267,RMVar_hsa_circ_186697,RMVar_hsa_circ_186698,RMVar_hsa_circ_41049,RMVar_hsa_circ_298433,RMVar_hsa_circ_55441,RMVar_hsa_circ_105974,RMVar_hsa_circ_76313,RMVar_hsa_circ_186703,RMVar_hsa_circ_186704,RMVar_hsa_circ_334229,RMVar_hsa_circ_335864,RMVar_hsa_circ_364763,RMVar_hsa_circ_318138,RMVar_hsa_circ_270983,RMVar_hsa_circ_284543,RMVar_hsa_circ_291983,RMVar_hsa_circ_42694,RMVar_hsa_circ_77993,RMVar_hsa_circ_39489,RMVar_hsa_circ_50642,RMVar_hsa_circ_186705,RMVar_hsa_circ_186709,RMVar_hsa_circ_186711,RMVar_hsa_circ_30380,RMVar_hsa_circ_186710,RMVar_hsa_circ_186707,RMVar_hsa_circ_186708,RMVar_hsa_circ_186706,RMVar_hsa_circ_309665,RMVar_hsa_circ_348399,RMVar_hsa_circ_362667,RMVar_hsa_circ_186713,RMVar_hsa_circ_355492,RMVar_hsa_circ_324311,RMVar_hsa_circ_305218,RMVar_hsa_circ_286497,RMVar_hsa_circ_64813,RMVar_hsa_circ_67636,RMVar_hsa_circ_58551,RMVar_hsa_circ_186714,RMVar_hsa_circ_186716,RMVar_hsa_circ_186718,RMVar_hsa_circ_46250,RMVar_hsa_circ_186717,RMVar_hsa_circ_186715,RMVar_hsa_circ_112902,RMVar_hsa_circ_113175,RMVar_hsa_circ_77308,RMVar_hsa_circ_118894,RMVar_hsa_circ_186721,RMVar_hsa_circ_186722,RMVar_hsa_circ_186723,RMVar_hsa_circ_186724,RMVar_hsa_circ_56273,RMVar_hsa_circ_95566,RMVar_hsa_circ_186725 40996 RMVar_ID_40996 Human_SNP_ID_630889202 A-to-I Human chr17 + 67900244 67900244 67900244 CTCCTGCCTCAGCCTGCTGAGTAGCTGGGATTACAGACAAGTACCACAATGCCCGGCTAATTTTC CTCCTGCCTCAGCCTGCTGAGTAGCTGGGATTGCAGACAAGTACCACAATGCCCGGCTAATTTTC A G BPTF Ensembl:ENSG00000171634 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1047614228 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74181,RMVar_hsa_circ_105707,RMVar_hsa_circ_115820,RMVar_hsa_circ_112988,RMVar_hsa_circ_96942,RMVar_hsa_circ_97433,RMVar_hsa_circ_104065,RMVar_hsa_circ_186692,RMVar_hsa_circ_186694,RMVar_hsa_circ_186695,RMVar_hsa_circ_186693,RMVar_hsa_circ_186691,RMVar_hsa_circ_101267,RMVar_hsa_circ_186697,RMVar_hsa_circ_186698,RMVar_hsa_circ_41049,RMVar_hsa_circ_298433,RMVar_hsa_circ_55441,RMVar_hsa_circ_105974,RMVar_hsa_circ_76313,RMVar_hsa_circ_186703,RMVar_hsa_circ_186704,RMVar_hsa_circ_334229,RMVar_hsa_circ_335864,RMVar_hsa_circ_364763,RMVar_hsa_circ_318138,RMVar_hsa_circ_270983,RMVar_hsa_circ_284543,RMVar_hsa_circ_291983,RMVar_hsa_circ_42694,RMVar_hsa_circ_77993,RMVar_hsa_circ_39489,RMVar_hsa_circ_50642,RMVar_hsa_circ_186705,RMVar_hsa_circ_186709,RMVar_hsa_circ_186711,RMVar_hsa_circ_30380,RMVar_hsa_circ_186710,RMVar_hsa_circ_186707,RMVar_hsa_circ_186708,RMVar_hsa_circ_186706,RMVar_hsa_circ_309665,RMVar_hsa_circ_348399,RMVar_hsa_circ_362667,RMVar_hsa_circ_186713,RMVar_hsa_circ_355492,RMVar_hsa_circ_324311,RMVar_hsa_circ_305218,RMVar_hsa_circ_286497,RMVar_hsa_circ_64813,RMVar_hsa_circ_67636,RMVar_hsa_circ_58551,RMVar_hsa_circ_186714,RMVar_hsa_circ_186716,RMVar_hsa_circ_186718,RMVar_hsa_circ_46250,RMVar_hsa_circ_186717,RMVar_hsa_circ_186715,RMVar_hsa_circ_112902,RMVar_hsa_circ_113175,RMVar_hsa_circ_77308,RMVar_hsa_circ_118894,RMVar_hsa_circ_186721,RMVar_hsa_circ_186722,RMVar_hsa_circ_186723,RMVar_hsa_circ_186724,RMVar_hsa_circ_56273,RMVar_hsa_circ_95566,RMVar_hsa_circ_186725 40997 RMVar_ID_40997 Human_SNP_ID_630889218 A-to-I Human chr17 + 67900285 67900285 67900285 TACCACAATGCCCGGCTAATTTTCGTATTTTTAGTAGAGATGGGGTTTTGTCGTGTTGGCCAGGC TACCACAATGCCCGGCTAATTTTCGTATTTTTGGTAGAGATGGGGTTTTGTCGTGTTGGCCAGGC A G BPTF Ensembl:ENSG00000171634 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1323844203 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74181,RMVar_hsa_circ_105707,RMVar_hsa_circ_115820,RMVar_hsa_circ_112988,RMVar_hsa_circ_96942,RMVar_hsa_circ_97433,RMVar_hsa_circ_104065,RMVar_hsa_circ_186692,RMVar_hsa_circ_186694,RMVar_hsa_circ_186695,RMVar_hsa_circ_186693,RMVar_hsa_circ_186691,RMVar_hsa_circ_101267,RMVar_hsa_circ_186697,RMVar_hsa_circ_186698,RMVar_hsa_circ_41049,RMVar_hsa_circ_298433,RMVar_hsa_circ_55441,RMVar_hsa_circ_105974,RMVar_hsa_circ_76313,RMVar_hsa_circ_186703,RMVar_hsa_circ_186704,RMVar_hsa_circ_334229,RMVar_hsa_circ_335864,RMVar_hsa_circ_364763,RMVar_hsa_circ_318138,RMVar_hsa_circ_270983,RMVar_hsa_circ_284543,RMVar_hsa_circ_291983,RMVar_hsa_circ_42694,RMVar_hsa_circ_77993,RMVar_hsa_circ_39489,RMVar_hsa_circ_50642,RMVar_hsa_circ_186705,RMVar_hsa_circ_186709,RMVar_hsa_circ_186711,RMVar_hsa_circ_30380,RMVar_hsa_circ_186710,RMVar_hsa_circ_186707,RMVar_hsa_circ_186708,RMVar_hsa_circ_186706,RMVar_hsa_circ_309665,RMVar_hsa_circ_348399,RMVar_hsa_circ_362667,RMVar_hsa_circ_186713,RMVar_hsa_circ_355492,RMVar_hsa_circ_324311,RMVar_hsa_circ_305218,RMVar_hsa_circ_286497,RMVar_hsa_circ_64813,RMVar_hsa_circ_67636,RMVar_hsa_circ_58551,RMVar_hsa_circ_186714,RMVar_hsa_circ_186716,RMVar_hsa_circ_186718,RMVar_hsa_circ_46250,RMVar_hsa_circ_186717,RMVar_hsa_circ_186715,RMVar_hsa_circ_112902,RMVar_hsa_circ_113175,RMVar_hsa_circ_77308,RMVar_hsa_circ_118894,RMVar_hsa_circ_186721,RMVar_hsa_circ_186722,RMVar_hsa_circ_186723,RMVar_hsa_circ_186724,RMVar_hsa_circ_56273,RMVar_hsa_circ_95566,RMVar_hsa_circ_186725 40998 RMVar_ID_40998 Human_SNP_ID_630890423 A-to-I Human chr17 + 67905253 67905253 67905253 TAACATGGTGAAACCCTGTCTCTACTAAAAATACAAAATTTGCTGGGTGTGCTGGTACACGCCTG TAACATGGTGAAACCCTGTCTCTACTAAAAATGCAAAATTTGCTGGGTGTGCTGGTACACGCCTG A G BPTF Ensembl:ENSG00000171634 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1222409105 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74181,RMVar_hsa_circ_105707,RMVar_hsa_circ_115820,RMVar_hsa_circ_112988,RMVar_hsa_circ_96942,RMVar_hsa_circ_97433,RMVar_hsa_circ_104065,RMVar_hsa_circ_186692,RMVar_hsa_circ_186694,RMVar_hsa_circ_186695,RMVar_hsa_circ_186693,RMVar_hsa_circ_186691,RMVar_hsa_circ_186697,RMVar_hsa_circ_41049,RMVar_hsa_circ_298433,RMVar_hsa_circ_55441,RMVar_hsa_circ_105974,RMVar_hsa_circ_76313,RMVar_hsa_circ_186703,RMVar_hsa_circ_186704,RMVar_hsa_circ_335864,RMVar_hsa_circ_364763,RMVar_hsa_circ_318138,RMVar_hsa_circ_270983,RMVar_hsa_circ_284543,RMVar_hsa_circ_291983,RMVar_hsa_circ_77993,RMVar_hsa_circ_39489,RMVar_hsa_circ_50642,RMVar_hsa_circ_186705,RMVar_hsa_circ_186709,RMVar_hsa_circ_186711,RMVar_hsa_circ_30380,RMVar_hsa_circ_186710,RMVar_hsa_circ_186707,RMVar_hsa_circ_186708,RMVar_hsa_circ_186706,RMVar_hsa_circ_348399,RMVar_hsa_circ_362667,RMVar_hsa_circ_355492,RMVar_hsa_circ_324311,RMVar_hsa_circ_305218,RMVar_hsa_circ_64813,RMVar_hsa_circ_67636,RMVar_hsa_circ_58551,RMVar_hsa_circ_186714,RMVar_hsa_circ_186716,RMVar_hsa_circ_46250,RMVar_hsa_circ_186715,RMVar_hsa_circ_112902,RMVar_hsa_circ_113175,RMVar_hsa_circ_77308,RMVar_hsa_circ_56529,RMVar_hsa_circ_118894,RMVar_hsa_circ_186721,RMVar_hsa_circ_186722,RMVar_hsa_circ_186723,RMVar_hsa_circ_186724,RMVar_hsa_circ_56273,RMVar_hsa_circ_95566,RMVar_hsa_circ_186725,RMVar_hsa_circ_127142,RMVar_hsa_circ_331695,RMVar_hsa_circ_351769,RMVar_hsa_circ_1689,RMVar_hsa_circ_186726,RMVar_hsa_circ_34915,RMVar_hsa_circ_329089,RMVar_hsa_circ_186727 40999 RMVar_ID_40999 Human_SNP_ID_630890494 A-to-I Human chr17 + 67905525 67905525 67905525 GGCCAGGAGTTCAAGGCCAGCCTGGGCAACATAGCAAGACCCCATCTCTACAAAAACGTTTTAAA GGCCAGGAGTTCAAGGCCAGCCTGGGCAACATGGCAAGACCCCATCTCTACAAAAACGTTTTAAA A G BPTF Ensembl:ENSG00000171634 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1417454866 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74181,RMVar_hsa_circ_105707,RMVar_hsa_circ_115820,RMVar_hsa_circ_112988,RMVar_hsa_circ_96942,RMVar_hsa_circ_97433,RMVar_hsa_circ_104065,RMVar_hsa_circ_186692,RMVar_hsa_circ_186694,RMVar_hsa_circ_186695,RMVar_hsa_circ_186693,RMVar_hsa_circ_186691,RMVar_hsa_circ_186697,RMVar_hsa_circ_41049,RMVar_hsa_circ_298433,RMVar_hsa_circ_55441,RMVar_hsa_circ_105974,RMVar_hsa_circ_76313,RMVar_hsa_circ_186703,RMVar_hsa_circ_186704,RMVar_hsa_circ_335864,RMVar_hsa_circ_364763,RMVar_hsa_circ_318138,RMVar_hsa_circ_270983,RMVar_hsa_circ_284543,RMVar_hsa_circ_291983,RMVar_hsa_circ_77993,RMVar_hsa_circ_39489,RMVar_hsa_circ_50642,RMVar_hsa_circ_186705,RMVar_hsa_circ_186709,RMVar_hsa_circ_186711,RMVar_hsa_circ_30380,RMVar_hsa_circ_186710,RMVar_hsa_circ_186707,RMVar_hsa_circ_186708,RMVar_hsa_circ_186706,RMVar_hsa_circ_348399,RMVar_hsa_circ_362667,RMVar_hsa_circ_355492,RMVar_hsa_circ_324311,RMVar_hsa_circ_305218,RMVar_hsa_circ_64813,RMVar_hsa_circ_67636,RMVar_hsa_circ_58551,RMVar_hsa_circ_186714,RMVar_hsa_circ_186716,RMVar_hsa_circ_46250,RMVar_hsa_circ_186715,RMVar_hsa_circ_112902,RMVar_hsa_circ_113175,RMVar_hsa_circ_77308,RMVar_hsa_circ_56529,RMVar_hsa_circ_118894,RMVar_hsa_circ_186721,RMVar_hsa_circ_186722,RMVar_hsa_circ_186723,RMVar_hsa_circ_186724,RMVar_hsa_circ_56273,RMVar_hsa_circ_95566,RMVar_hsa_circ_186725,RMVar_hsa_circ_127142,RMVar_hsa_circ_331695,RMVar_hsa_circ_351769,RMVar_hsa_circ_1689,RMVar_hsa_circ_186726,RMVar_hsa_circ_34915,RMVar_hsa_circ_329089,RMVar_hsa_circ_186727 41000 RMVar_ID_41000 Human_SNP_ID_630890859 A-to-I Human chr17 + 67907054 67907054 67907054 AAAAAATGCAAAAATTAGCCAGACATATTGGTACACACCTGTATTCCCAGTTACTCAGGAGGCTG AAAAAATGCAAAAATTAGCCAGACATATTGGTGCACACCTGTATTCCCAGTTACTCAGGAGGCTG A G BPTF Ensembl:ENSG00000171634 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270073697 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74181,RMVar_hsa_circ_105707,RMVar_hsa_circ_115820,RMVar_hsa_circ_112988,RMVar_hsa_circ_96942,RMVar_hsa_circ_97433,RMVar_hsa_circ_104065,RMVar_hsa_circ_186692,RMVar_hsa_circ_186694,RMVar_hsa_circ_186695,RMVar_hsa_circ_186693,RMVar_hsa_circ_186691,RMVar_hsa_circ_186697,RMVar_hsa_circ_41049,RMVar_hsa_circ_298433,RMVar_hsa_circ_55441,RMVar_hsa_circ_105974,RMVar_hsa_circ_76313,RMVar_hsa_circ_186703,RMVar_hsa_circ_186704,RMVar_hsa_circ_335864,RMVar_hsa_circ_364763,RMVar_hsa_circ_318138,RMVar_hsa_circ_270983,RMVar_hsa_circ_284543,RMVar_hsa_circ_291983,RMVar_hsa_circ_77993,RMVar_hsa_circ_39489,RMVar_hsa_circ_50642,RMVar_hsa_circ_186705,RMVar_hsa_circ_186709,RMVar_hsa_circ_186711,RMVar_hsa_circ_30380,RMVar_hsa_circ_186710,RMVar_hsa_circ_186707,RMVar_hsa_circ_186708,RMVar_hsa_circ_186706,RMVar_hsa_circ_348399,RMVar_hsa_circ_362667,RMVar_hsa_circ_355492,RMVar_hsa_circ_324311,RMVar_hsa_circ_305218,RMVar_hsa_circ_64813,RMVar_hsa_circ_67636,RMVar_hsa_circ_58551,RMVar_hsa_circ_186714,RMVar_hsa_circ_186716,RMVar_hsa_circ_46250,RMVar_hsa_circ_186715,RMVar_hsa_circ_112902,RMVar_hsa_circ_113175,RMVar_hsa_circ_77308,RMVar_hsa_circ_56529,RMVar_hsa_circ_118894,RMVar_hsa_circ_186721,RMVar_hsa_circ_186722,RMVar_hsa_circ_186723,RMVar_hsa_circ_186724,RMVar_hsa_circ_56273,RMVar_hsa_circ_95566,RMVar_hsa_circ_186725,RMVar_hsa_circ_127142,RMVar_hsa_circ_331695,RMVar_hsa_circ_351769,RMVar_hsa_circ_1689,RMVar_hsa_circ_186726,RMVar_hsa_circ_34915,RMVar_hsa_circ_329089,RMVar_hsa_circ_186727 41001 RMVar_ID_41001 Human_SNP_ID_630891210 A-to-I Human chr17 + 67908288 67908288 67908288 TGAAGCAATTCTCCTGCTTCAGTCTCCCAAGTAGCTGGGACTACAGGCTCGTACCACCATGACTG TGAAGCAATTCTCCTGCTTCAGTCTCCCAAGTGGCTGGGACTACAGGCTCGTACCACCATGACTG A G BPTF Ensembl:ENSG00000171634 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1489092855 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74181,RMVar_hsa_circ_105707,RMVar_hsa_circ_115820,RMVar_hsa_circ_112988,RMVar_hsa_circ_96942,RMVar_hsa_circ_97433,RMVar_hsa_circ_104065,RMVar_hsa_circ_186692,RMVar_hsa_circ_186694,RMVar_hsa_circ_186695,RMVar_hsa_circ_186693,RMVar_hsa_circ_186691,RMVar_hsa_circ_186697,RMVar_hsa_circ_41049,RMVar_hsa_circ_298433,RMVar_hsa_circ_55441,RMVar_hsa_circ_105974,RMVar_hsa_circ_76313,RMVar_hsa_circ_186703,RMVar_hsa_circ_186704,RMVar_hsa_circ_335864,RMVar_hsa_circ_364763,RMVar_hsa_circ_318138,RMVar_hsa_circ_270983,RMVar_hsa_circ_284543,RMVar_hsa_circ_291983,RMVar_hsa_circ_77993,RMVar_hsa_circ_39489,RMVar_hsa_circ_50642,RMVar_hsa_circ_186705,RMVar_hsa_circ_186709,RMVar_hsa_circ_186711,RMVar_hsa_circ_30380,RMVar_hsa_circ_186710,RMVar_hsa_circ_186707,RMVar_hsa_circ_186708,RMVar_hsa_circ_186706,RMVar_hsa_circ_348399,RMVar_hsa_circ_362667,RMVar_hsa_circ_355492,RMVar_hsa_circ_324311,RMVar_hsa_circ_305218,RMVar_hsa_circ_64813,RMVar_hsa_circ_67636,RMVar_hsa_circ_58551,RMVar_hsa_circ_186714,RMVar_hsa_circ_186716,RMVar_hsa_circ_46250,RMVar_hsa_circ_186715,RMVar_hsa_circ_112902,RMVar_hsa_circ_113175,RMVar_hsa_circ_77308,RMVar_hsa_circ_56529,RMVar_hsa_circ_118894,RMVar_hsa_circ_186721,RMVar_hsa_circ_186722,RMVar_hsa_circ_186723,RMVar_hsa_circ_186724,RMVar_hsa_circ_56273,RMVar_hsa_circ_95566,RMVar_hsa_circ_186725,RMVar_hsa_circ_127142,RMVar_hsa_circ_331695,RMVar_hsa_circ_351769,RMVar_hsa_circ_1689,RMVar_hsa_circ_186726,RMVar_hsa_circ_34915,RMVar_hsa_circ_329089,RMVar_hsa_circ_186727 41002 RMVar_ID_41002 Human_SNP_ID_630891417 A-to-I Human chr17 + 67908964 67908964 67908964 TCAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCTGAGATCACAGGTGTGCACCACCACACCCA TCAAGCAATTCTCCTGCCTCAGCCTCCTGAGTGGCTGAGATCACAGGTGTGCACCACCACACCCA A G BPTF Ensembl:ENSG00000171634 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs575896681 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74181,RMVar_hsa_circ_105707,RMVar_hsa_circ_115820,RMVar_hsa_circ_112988,RMVar_hsa_circ_96942,RMVar_hsa_circ_97433,RMVar_hsa_circ_104065,RMVar_hsa_circ_186692,RMVar_hsa_circ_186694,RMVar_hsa_circ_186695,RMVar_hsa_circ_186693,RMVar_hsa_circ_186691,RMVar_hsa_circ_186697,RMVar_hsa_circ_41049,RMVar_hsa_circ_298433,RMVar_hsa_circ_55441,RMVar_hsa_circ_105974,RMVar_hsa_circ_76313,RMVar_hsa_circ_186703,RMVar_hsa_circ_186704,RMVar_hsa_circ_335864,RMVar_hsa_circ_364763,RMVar_hsa_circ_318138,RMVar_hsa_circ_270983,RMVar_hsa_circ_284543,RMVar_hsa_circ_291983,RMVar_hsa_circ_77993,RMVar_hsa_circ_39489,RMVar_hsa_circ_50642,RMVar_hsa_circ_186705,RMVar_hsa_circ_186709,RMVar_hsa_circ_186711,RMVar_hsa_circ_30380,RMVar_hsa_circ_186710,RMVar_hsa_circ_186707,RMVar_hsa_circ_186708,RMVar_hsa_circ_186706,RMVar_hsa_circ_348399,RMVar_hsa_circ_362667,RMVar_hsa_circ_355492,RMVar_hsa_circ_324311,RMVar_hsa_circ_305218,RMVar_hsa_circ_64813,RMVar_hsa_circ_67636,RMVar_hsa_circ_58551,RMVar_hsa_circ_186714,RMVar_hsa_circ_186716,RMVar_hsa_circ_46250,RMVar_hsa_circ_186715,RMVar_hsa_circ_112902,RMVar_hsa_circ_113175,RMVar_hsa_circ_77308,RMVar_hsa_circ_56529,RMVar_hsa_circ_118894,RMVar_hsa_circ_186721,RMVar_hsa_circ_186722,RMVar_hsa_circ_186723,RMVar_hsa_circ_186724,RMVar_hsa_circ_56273,RMVar_hsa_circ_95566,RMVar_hsa_circ_186725,RMVar_hsa_circ_127142,RMVar_hsa_circ_331695,RMVar_hsa_circ_351769,RMVar_hsa_circ_1689,RMVar_hsa_circ_186726,RMVar_hsa_circ_34915,RMVar_hsa_circ_329089,RMVar_hsa_circ_186727 41003 RMVar_ID_41003 Human_SNP_ID_630902305 A-to-I Human chr17 + 67950676 67950676 67950676 CCTGATCAAGATGGTGAAACCCCATCTCTACTAAAAATACAAAAAAATTAGTCAGGCATGGTGGT CCTGATCAAGATGGTGAAACCCCATCTCTACTGAAAATACAAAAAAATTAGTCAGGCATGGTGGT A G BPTF Ensembl:ENSG00000171634 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs747800771 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74181,RMVar_hsa_circ_298433,RMVar_hsa_circ_55441,RMVar_hsa_circ_77993,RMVar_hsa_circ_186705,RMVar_hsa_circ_186706,RMVar_hsa_circ_324311,RMVar_hsa_circ_112902,RMVar_hsa_circ_113175,RMVar_hsa_circ_186722,RMVar_hsa_circ_186723,RMVar_hsa_circ_351769,RMVar_hsa_circ_57588,RMVar_hsa_circ_268184,RMVar_hsa_circ_71713,RMVar_hsa_circ_42616,RMVar_hsa_circ_372814,RMVar_hsa_circ_375659,RMVar_hsa_circ_105800,RMVar_hsa_circ_77894,RMVar_hsa_circ_186746,RMVar_hsa_circ_186747,RMVar_hsa_circ_186744,RMVar_hsa_circ_186745,RMVar_hsa_circ_48311,RMVar_hsa_circ_92140,RMVar_hsa_circ_355915,RMVar_hsa_circ_186752,RMVar_hsa_circ_378211,RMVar_hsa_circ_69189,RMVar_hsa_circ_277900,RMVar_hsa_circ_288063,RMVar_hsa_circ_353230,RMVar_hsa_circ_282885,RMVar_hsa_circ_186756,RMVar_hsa_circ_186757,RMVar_hsa_circ_186755,RMVar_hsa_circ_32090,RMVar_hsa_circ_186759,RMVar_hsa_circ_306916,RMVar_hsa_circ_74294,RMVar_hsa_circ_350921 41004 RMVar_ID_41004 Human_SNP_ID_630902393 A-to-I Human chr17 + 67951052 67951052 67951052 GCTGGTCTCGAACTCCTGGCCTCAAGTAATCCACCCGCCTTAGTCTCCCAAAGTCCTGGGATTAC GCTGGTCTCGAACTCCTGGCCTCAAGTAATCCCCCCGCCTTAGTCTCCCAAAGTCCTGGGATTAC A C BPTF Ensembl:ENSG00000171634 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1555678337 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74181,RMVar_hsa_circ_298433,RMVar_hsa_circ_55441,RMVar_hsa_circ_77993,RMVar_hsa_circ_186705,RMVar_hsa_circ_186706,RMVar_hsa_circ_324311,RMVar_hsa_circ_112902,RMVar_hsa_circ_113175,RMVar_hsa_circ_186722,RMVar_hsa_circ_186723,RMVar_hsa_circ_351769,RMVar_hsa_circ_57588,RMVar_hsa_circ_268184,RMVar_hsa_circ_71713,RMVar_hsa_circ_42616,RMVar_hsa_circ_372814,RMVar_hsa_circ_375659,RMVar_hsa_circ_105800,RMVar_hsa_circ_77894,RMVar_hsa_circ_186746,RMVar_hsa_circ_186747,RMVar_hsa_circ_186744,RMVar_hsa_circ_186745,RMVar_hsa_circ_48311,RMVar_hsa_circ_92140,RMVar_hsa_circ_355915,RMVar_hsa_circ_186752,RMVar_hsa_circ_378211,RMVar_hsa_circ_69189,RMVar_hsa_circ_277900,RMVar_hsa_circ_288063,RMVar_hsa_circ_353230,RMVar_hsa_circ_282885,RMVar_hsa_circ_186756,RMVar_hsa_circ_186757,RMVar_hsa_circ_186755,RMVar_hsa_circ_32090,RMVar_hsa_circ_186759,RMVar_hsa_circ_306916,RMVar_hsa_circ_74294,RMVar_hsa_circ_350921 41005 RMVar_ID_41005 Human_SNP_ID_630902444 A-to-I Human chr17 + 67951258 67951258 67951258 AGGTGGCACTGAAAGCCCTGAGAATCAGCCCCAATCCTGAGGCTCTCTAGGAGCCTCCAGCCATC AGGTGGCACTGAAAGCCCTGAGAATCAGCCCCGATCCTGAGGCTCTCTAGGAGCCTCCAGCCATC A G BPTF Ensembl:ENSG00000171634 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7502482 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74181,RMVar_hsa_circ_298433,RMVar_hsa_circ_55441,RMVar_hsa_circ_77993,RMVar_hsa_circ_186705,RMVar_hsa_circ_186706,RMVar_hsa_circ_324311,RMVar_hsa_circ_112902,RMVar_hsa_circ_113175,RMVar_hsa_circ_186722,RMVar_hsa_circ_186723,RMVar_hsa_circ_351769,RMVar_hsa_circ_57588,RMVar_hsa_circ_268184,RMVar_hsa_circ_71713,RMVar_hsa_circ_42616,RMVar_hsa_circ_372814,RMVar_hsa_circ_375659,RMVar_hsa_circ_105800,RMVar_hsa_circ_77894,RMVar_hsa_circ_186746,RMVar_hsa_circ_186747,RMVar_hsa_circ_186744,RMVar_hsa_circ_186745,RMVar_hsa_circ_48311,RMVar_hsa_circ_92140,RMVar_hsa_circ_355915,RMVar_hsa_circ_186752,RMVar_hsa_circ_378211,RMVar_hsa_circ_69189,RMVar_hsa_circ_277900,RMVar_hsa_circ_288063,RMVar_hsa_circ_353230,RMVar_hsa_circ_282885,RMVar_hsa_circ_186756,RMVar_hsa_circ_186757,RMVar_hsa_circ_186755,RMVar_hsa_circ_32090,RMVar_hsa_circ_186759,RMVar_hsa_circ_306916,RMVar_hsa_circ_74294,RMVar_hsa_circ_350921 41006 RMVar_ID_41006 Human_SNP_ID_630903939 A-to-I Human chr17 + 67956457 67956457 67956457 CTCCCACCTCAGCCTTCCAAGTAGCTGGCACTATAGGCATGTGCCACCACACCTGGCTGATTTTT CTCCCACCTCAGCCTTCCAAGTAGCTGGCACTGTAGGCATGTGCCACCACACCTGGCTGATTTTT A G AC134407.2,BPTF Ensembl:ENSG00000279573,Ensembl:ENSG00000171634 Other,Protein coding exon,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs118033764 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74181,RMVar_hsa_circ_298433,RMVar_hsa_circ_55441,RMVar_hsa_circ_77993,RMVar_hsa_circ_186705,RMVar_hsa_circ_186706,RMVar_hsa_circ_324311,RMVar_hsa_circ_112902,RMVar_hsa_circ_113175,RMVar_hsa_circ_186722,RMVar_hsa_circ_186723,RMVar_hsa_circ_351769,RMVar_hsa_circ_57588,RMVar_hsa_circ_268184,RMVar_hsa_circ_71713,RMVar_hsa_circ_42616,RMVar_hsa_circ_372814,RMVar_hsa_circ_375659,RMVar_hsa_circ_105800,RMVar_hsa_circ_77894,RMVar_hsa_circ_186746,RMVar_hsa_circ_186747,RMVar_hsa_circ_186744,RMVar_hsa_circ_186745,RMVar_hsa_circ_48311,RMVar_hsa_circ_92140,RMVar_hsa_circ_355915,RMVar_hsa_circ_186752,RMVar_hsa_circ_378211,RMVar_hsa_circ_69189,RMVar_hsa_circ_277900,RMVar_hsa_circ_288063,RMVar_hsa_circ_353230,RMVar_hsa_circ_282885,RMVar_hsa_circ_186756,RMVar_hsa_circ_186757,RMVar_hsa_circ_186755,RMVar_hsa_circ_32090,RMVar_hsa_circ_186759,RMVar_hsa_circ_306916,RMVar_hsa_circ_74294,RMVar_hsa_circ_350921 41007 RMVar_ID_41007 Human_SNP_ID_630904068 A-to-I Human chr17 + 67956853 67956853 67956853 GAGTGTGGTGGCGGGCGCATGTAGCCCCAGCTACTCAGTAGGCTGAGGCAGGAGAATGGCATGAA GAGTGTGGTGGCGGGCGCATGTAGCCCCAGCTGCTCAGTAGGCTGAGGCAGGAGAATGGCATGAA A G AC134407.2,BPTF Ensembl:ENSG00000279573,Ensembl:ENSG00000171634 Other,Protein coding exon,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1384510535 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74181,RMVar_hsa_circ_298433,RMVar_hsa_circ_55441,RMVar_hsa_circ_77993,RMVar_hsa_circ_186705,RMVar_hsa_circ_186706,RMVar_hsa_circ_324311,RMVar_hsa_circ_112902,RMVar_hsa_circ_113175,RMVar_hsa_circ_186722,RMVar_hsa_circ_186723,RMVar_hsa_circ_351769,RMVar_hsa_circ_57588,RMVar_hsa_circ_268184,RMVar_hsa_circ_71713,RMVar_hsa_circ_42616,RMVar_hsa_circ_372814,RMVar_hsa_circ_375659,RMVar_hsa_circ_105800,RMVar_hsa_circ_77894,RMVar_hsa_circ_186746,RMVar_hsa_circ_186747,RMVar_hsa_circ_186744,RMVar_hsa_circ_186745,RMVar_hsa_circ_48311,RMVar_hsa_circ_92140,RMVar_hsa_circ_355915,RMVar_hsa_circ_186752,RMVar_hsa_circ_378211,RMVar_hsa_circ_69189,RMVar_hsa_circ_277900,RMVar_hsa_circ_288063,RMVar_hsa_circ_353230,RMVar_hsa_circ_282885,RMVar_hsa_circ_186756,RMVar_hsa_circ_186757,RMVar_hsa_circ_186755,RMVar_hsa_circ_32090,RMVar_hsa_circ_186759,RMVar_hsa_circ_306916,RMVar_hsa_circ_74294,RMVar_hsa_circ_350921 41008 RMVar_ID_41008 Human_SNP_ID_630906908 A-to-I Human chr17 + 67967362 67967362 67967362 CAGGGTTTCACCATGTTGGCCAGGATGGTCTCAATCTCCTGACCTTGTGATCCGCTCCCCCTCGG CAGGGTTTCACCATGTTGGCCAGGATGGTCTCGATCTCCTGACCTTGTGATCCGCTCCCCCTCGG A G BPTF Ensembl:ENSG00000171634 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1330394259 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48,RMVar_hsa_circ_74181,RMVar_hsa_circ_298433,RMVar_hsa_circ_55441,RMVar_hsa_circ_186705,RMVar_hsa_circ_324311,RMVar_hsa_circ_113175,RMVar_hsa_circ_186723,RMVar_hsa_circ_351769,RMVar_hsa_circ_57588,RMVar_hsa_circ_71713,RMVar_hsa_circ_372814,RMVar_hsa_circ_186744,RMVar_hsa_circ_48311,RMVar_hsa_circ_355915,RMVar_hsa_circ_277900,RMVar_hsa_circ_186757,RMVar_hsa_circ_186759,RMVar_hsa_circ_306916,RMVar_hsa_circ_350921,RMVar_hsa_circ_66730,RMVar_hsa_circ_186760,RMVar_hsa_circ_296250,RMVar_hsa_circ_186762,RMVar_hsa_circ_285319 41009 RMVar_ID_41009 Human_SNP_ID_630907953 A-to-I Human chr17 + 67971264 67971264 67971264 CCACACCCAGCTAATTTTTGTATTTTTGGTAGAATCAGGGTTTCACCATGTTGGCCAGGCTGATC CCACACCCAGCTAATTTTTGTATTTTTGGTAGGATCAGGGTTTCACCATGTTGGCCAGGCTGATC A G BPTF Ensembl:ENSG00000171634 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1455023875 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48,RMVar_hsa_circ_74181,RMVar_hsa_circ_298433,RMVar_hsa_circ_55441,RMVar_hsa_circ_186705,RMVar_hsa_circ_324311,RMVar_hsa_circ_113175,RMVar_hsa_circ_186723,RMVar_hsa_circ_351769,RMVar_hsa_circ_57588,RMVar_hsa_circ_71713,RMVar_hsa_circ_372814,RMVar_hsa_circ_186744,RMVar_hsa_circ_48311,RMVar_hsa_circ_355915,RMVar_hsa_circ_277900,RMVar_hsa_circ_186757,RMVar_hsa_circ_186759,RMVar_hsa_circ_306916,RMVar_hsa_circ_350921,RMVar_hsa_circ_66730,RMVar_hsa_circ_186760,RMVar_hsa_circ_296250,RMVar_hsa_circ_186762,RMVar_hsa_circ_285319 41010 RMVar_ID_41010 Human_SNP_ID_630907954 A-to-I Human chr17 + 67971264 67971264 67971264 CCACACCCAGCTAATTTTTGTATTTTTGGTAGAATCAGGGTTTCACCATGTTGGCCAGGCTGATC CCACACCCAGCTAATTTTTGTATTTTTGGTAGTATCAGGGTTTCACCATGTTGGCCAGGCTGATC A T BPTF Ensembl:ENSG00000171634 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1455023875 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48,RMVar_hsa_circ_74181,RMVar_hsa_circ_298433,RMVar_hsa_circ_55441,RMVar_hsa_circ_186705,RMVar_hsa_circ_324311,RMVar_hsa_circ_113175,RMVar_hsa_circ_186723,RMVar_hsa_circ_351769,RMVar_hsa_circ_57588,RMVar_hsa_circ_71713,RMVar_hsa_circ_372814,RMVar_hsa_circ_186744,RMVar_hsa_circ_48311,RMVar_hsa_circ_355915,RMVar_hsa_circ_277900,RMVar_hsa_circ_186757,RMVar_hsa_circ_186759,RMVar_hsa_circ_306916,RMVar_hsa_circ_350921,RMVar_hsa_circ_66730,RMVar_hsa_circ_186760,RMVar_hsa_circ_296250,RMVar_hsa_circ_186762,RMVar_hsa_circ_285319 41011 RMVar_ID_41011 Human_SNP_ID_630908233 A-to-I Human chr17 + 67972267 67972267 67972267 TTATTATTTTATTTTTTTTGAGAAGGAATCTCACTCTGTCACCCAGGCTGGAGTGCAGTGTCGTG TTATTATTTTATTTTTTTTGAGAAGGAATCTCGCTCTGTCACCCAGGCTGGAGTGCAGTGTCGTG A G BPTF Ensembl:ENSG00000171634 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1487760921 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48,RMVar_hsa_circ_74181,RMVar_hsa_circ_298433,RMVar_hsa_circ_55441,RMVar_hsa_circ_186705,RMVar_hsa_circ_324311,RMVar_hsa_circ_113175,RMVar_hsa_circ_186723,RMVar_hsa_circ_351769,RMVar_hsa_circ_57588,RMVar_hsa_circ_71713,RMVar_hsa_circ_372814,RMVar_hsa_circ_186744,RMVar_hsa_circ_48311,RMVar_hsa_circ_355915,RMVar_hsa_circ_277900,RMVar_hsa_circ_186757,RMVar_hsa_circ_186759,RMVar_hsa_circ_306916,RMVar_hsa_circ_350921,RMVar_hsa_circ_66730,RMVar_hsa_circ_186760,RMVar_hsa_circ_296250,RMVar_hsa_circ_186762,RMVar_hsa_circ_285319 41012 RMVar_ID_41012 Human_SNP_ID_630908650 A-to-I Human chr17 + 67973768 67973768 67973768 ACCTTGGATGATACGCCCACCTCGGCCTCCCAAACTGCTAGGATTACAGACGTGAGCCACCCCAG ACCTTGGATGATACGCCCACCTCGGCCTCCCATACTGCTAGGATTACAGACGTGAGCCACCCCAG A T BPTF Ensembl:ENSG00000171634 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1408460190 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48,RMVar_hsa_circ_74181,RMVar_hsa_circ_298433,RMVar_hsa_circ_55441,RMVar_hsa_circ_186705,RMVar_hsa_circ_324311,RMVar_hsa_circ_113175,RMVar_hsa_circ_186723,RMVar_hsa_circ_351769,RMVar_hsa_circ_57588,RMVar_hsa_circ_71713,RMVar_hsa_circ_372814,RMVar_hsa_circ_186744,RMVar_hsa_circ_48311,RMVar_hsa_circ_355915,RMVar_hsa_circ_277900,RMVar_hsa_circ_186757,RMVar_hsa_circ_186759,RMVar_hsa_circ_306916,RMVar_hsa_circ_350921,RMVar_hsa_circ_66730,RMVar_hsa_circ_186760,RMVar_hsa_circ_296250,RMVar_hsa_circ_186762,RMVar_hsa_circ_285319 41013 RMVar_ID_41013 Human_SNP_ID_630908652 A-to-I Human chr17 + 67973775 67973775 67973775 ATGATACGCCCACCTCGGCCTCCCAAACTGCTAGGATTACAGACGTGAGCCACCCCAGCCGCAAC ATGATACGCCCACCTCGGCCTCCCAAACTGCTGGGATTACAGACGTGAGCCACCCCAGCCGCAAC A G BPTF Ensembl:ENSG00000171634 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1555692333 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13146599 RMVar_hsa_circ_48,RMVar_hsa_circ_74181,RMVar_hsa_circ_298433,RMVar_hsa_circ_55441,RMVar_hsa_circ_186705,RMVar_hsa_circ_324311,RMVar_hsa_circ_113175,RMVar_hsa_circ_186723,RMVar_hsa_circ_351769,RMVar_hsa_circ_57588,RMVar_hsa_circ_71713,RMVar_hsa_circ_372814,RMVar_hsa_circ_186744,RMVar_hsa_circ_48311,RMVar_hsa_circ_355915,RMVar_hsa_circ_277900,RMVar_hsa_circ_186757,RMVar_hsa_circ_186759,RMVar_hsa_circ_306916,RMVar_hsa_circ_350921,RMVar_hsa_circ_66730,RMVar_hsa_circ_186760,RMVar_hsa_circ_296250,RMVar_hsa_circ_186762,RMVar_hsa_circ_285319 41014 RMVar_ID_41014 Human_SNP_ID_630909666 A-to-I Human chr17 + 67977378 67977378 67977378 CTCTCCTTAAAATACAAAAATTAGGCAGGCATAATGGTGCACGCCTGTAGTCTCAGCTACACAGG CTCTCCTTAAAATACAAAAATTAGGCAGGCATCATGGTGCACGCCTGTAGTCTCAGCTACACAGG A C BPTF Ensembl:ENSG00000171634 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1350377697 Functional Loss SNV dbSNP153 33..33 33 - - - 41015 RMVar_ID_41015 Human_SNP_ID_630912181 A-to-I Human chr17 + 67987004 67987004 67987004 GTGCTTGGCTGGGCGCGGTGGCTCACACCTGTAATCCCAGCACTTCGGGAGGCTGAGGCGGGCGG GTGCTTGGCTGGGCGCGGTGGCTCACACCTGTGATCCCAGCACTTCGGGAGGCTGAGGCGGGCGG A G MG828545 RNACentral:URS0000E4446F lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1394102430 Functional Loss SNV dbSNP153 33..33 33 - - - 41016 RMVar_ID_41016 Human_SNP_ID_630912647 A-to-I Human chr17 + 67988708 67988708 67988708 GCCTTGACCTCCTGGGCACAAGCCATCCTCCTACTTCAGCCTCCCAAGTAGCTGGGACCAAAGGC GCCTTGACCTCCTGGGCACAAGCCATCCTCCTGCTTCAGCCTCCCAAGTAGCTGGGACCAAAGGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355707841 Functional Loss SNV dbSNP153 33..33 33 - - - 41017 RMVar_ID_41017 Human_SNP_ID_630912944 A-to-I Human chr17 + 67989776 67989776 67989776 GCGACTCACTGCTACCTCTGCCTCCCGGATTCAAGCGATGCTCCTGCCTCAGCCTCCCGAGGAGC GCGACTCACTGCTACCTCTGCCTCCCGGATTCCAGCGATGCTCCTGCCTCAGCCTCCCGAGGAGC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs532500548 Functional Loss SNV dbSNP153 33..33 33 - - - 41018 RMVar_ID_41018 Human_SNP_ID_630913291 A-to-I Human chr17 - 67991325 67991321 67991326 GCAGATGGGTGGATTAAAAAAATAAATAAAATAAAAAATAGTACTAAAGGGCTTACTTCAGGCAA GCAGATGGGTGGATTAAAAAAATAAATAAAA_____AATAGTACTAAAGGGCTTACTTCAGGCAA TTTTTA T C17orf58 Ensembl:ENSG00000186665 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1221618876 Functional Loss DEL dbSNP153 32..36 33 - - - Human_RBP_ID_498102,Human_RBP_ID_3535856,Human_RBP_ID_17899779,Human_RBP_ID_25321541,Human_RBP_ID_27669158 RMVar_hsa_circ_96231,RMVar_hsa_circ_186764 41019 RMVar_ID_41019 Human_SNP_ID_630927022 A-to-I Human chr17 + 68039355 68039355 68039355 GTTTCCCAGTCTGGTCTCGAACTCCTGACCTCAGGTGATCCACCCGCCTCGGCCTCCCAAAGTGC GTTTCCCAGTCTGGTCTCGAACTCCTGACCTCGGGTGATCCACCCGCCTCGGCCTCCCAAAGTGC A G KPNA2 Ensembl:ENSG00000182481 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1171635478 Functional Loss SNV dbSNP153 33..33 33 - - - 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_35339,RMVar_hsa_circ_186767,RMVar_hsa_circ_186769,RMVar_hsa_circ_72740,RMVar_hsa_circ_186768,RMVar_hsa_circ_186766 41020 RMVar_ID_41020 Human_SNP_ID_630952006 A-to-I Human chr17 + 68115091 68115091 68115091 AGGGTCTCCCTCTGTCACCCAGGCTGGAGTGTAGTGGCGCGATCTCGGGTCACTGCAACCTCCCC AGGGTCTCCCTCTGTCACCCAGGCTGGAGTGTGGTGGCGCGATCTCGGGTCACTGCAACCTCCCC A G LINC00674 Ensembl:ENSG00000237854 Pseudogene exon GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 31158229,32596459 RNA-Seq:(High) rs1555713518 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1857914 RMVar_hsa_circ_186778,RMVar_hsa_circ_296546 41021 RMVar_ID_41021 Human_SNP_ID_630952044 A-to-I Human chr17 + 68115238 68115238 68115238 TTGTAATTTTTTTGTAGAGATGGGGTTTCGCCATGTTGCCTAGGCTGATCTCGAACTCCTGAGCT TTGTAATTTTTTTGTAGAGATGGGGTTTCGCCCTGTTGCCTAGGCTGATCTCGAACTCCTGAGCT A C LINC00674 Ensembl:ENSG00000237854 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1219024214 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_186778,RMVar_hsa_circ_296546 41022 RMVar_ID_41022 Human_SNP_ID_630952045 A-to-I Human chr17 + 68115238 68115238 68115238 TTGTAATTTTTTTGTAGAGATGGGGTTTCGCCATGTTGCCTAGGCTGATCTCGAACTCCTGAGCT TTGTAATTTTTTTGTAGAGATGGGGTTTCGCCTTGTTGCCTAGGCTGATCTCGAACTCCTGAGCT A T LINC00674 Ensembl:ENSG00000237854 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1219024214 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_186778,RMVar_hsa_circ_296546 41023 RMVar_ID_41023 Human_SNP_ID_630952053 A-to-I Human chr17 + 68115272 68115272 68115272 GTTGCCTAGGCTGATCTCGAACTCCTGAGCTCAAGTAGTCTGCCTGCCCCGGCCTCCCAAAGTGC GTTGCCTAGGCTGATCTCGAACTCCTGAGCTCGAGTAGTCTGCCTGCCCCGGCCTCCCAAAGTGC A G LINC00674 Ensembl:ENSG00000237854 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs564554962 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13147535 RMVar_hsa_circ_186778,RMVar_hsa_circ_296546 41024 RMVar_ID_41024 Human_SNP_ID_630952719 A-to-I Human chr17 + 68117314 68117314 68117314 GTGATCTTCTTGCCTCAGCCTCCTAAAGAGCTAGGACTATAGGCACATGCTTCTATGCCTATTAA GTGATCTTCTTGCCTCAGCCTCCTAAAGAGCTGGGACTATAGGCACATGCTTCTATGCCTATTAA A G LINC00674 RNACentral:URS000075B18A lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1456471835 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_186778,RMVar_hsa_circ_296546 41025 RMVar_ID_41025 Human_SNP_ID_630954904 A-to-I Human chr17 + 68126052 68126052 68126052 TCACCCAGGCTGGAGTACAGTGGTGTGATCACAGTTCACTGCAGACTCGACCTCCCTGGGCTCAG TCACCCAGGCTGGAGTACAGTGGTGTGATCACTGTTCACTGCAGACTCGACCTCCCTGGGCTCAG A T LINC00674 RNACentral:URS000075B18A lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs782038226 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13147612 41026 RMVar_ID_41026 Human_SNP_ID_630954937 A-to-I Human chr17 + 68126204 68126203 68126204 TAGGGTTTCACTATATTGGTCAAGCTGGTCTCAAACTCCTCTGACTTCAAGTGATCTACCCACCT TAGGGTTTCACTATATTGGTCAAGCTGGTCTC_AACTCCTCTGACTTCAAGTGATCTACCCACCT CA C LINC00674 RNACentral:URS000075B18A lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1220436599 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_498189,Human_RBP_ID_1183926,Human_RBP_ID_3535952,Human_RBP_ID_13147615,Human_RBP_ID_17261697,Human_RBP_ID_17377395,Human_RBP_ID_17493681,Human_RBP_ID_27456111 41027 RMVar_ID_41027 Human_SNP_ID_630955161 A-to-I Human chr17 + 68127213 68127213 68127213 CTATTGAGATAACTTTTCTTTCTCAATTTTCTAATCTTTTTGGCCTTGGGTGTTCTGTGGGCCAC CTATTGAGATAACTTTTCTTTCTCAATTTTCTGATCTTTTTGGCCTTGGGTGTTCTGTGGGCCAC A G AC005332.6 Ensembl:ENSG00000278730 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1271188841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6639521,Human_RBP_ID_17126498,Human_RBP_ID_17899834 41028 RMVar_ID_41028 Human_SNP_ID_630957714 A-to-I Human chr17 + 68137484 68137484 68137484 ATTTACGTATTTAATTTTTGAGATAGCATCTCACTCTGTGACCCAGGCTGGACTGCAGTGGTGAT ATTTACGTATTTAATTTTTGAGATAGCATCTCGCTCTGTGACCCAGGCTGGACTGCAGTGGTGAT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1275666680 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13147806 41029 RMVar_ID_41029 Human_SNP_ID_630958906 A-to-I Human chr17 + 68141990 68141989 68141991 GTGATCCATCCCCCTTGGCCTACCAAAGTGTTAAGATTACAGGCGTGAGCCACTGCACCTGACTG GTGATCCATCCCCCTTGGCCTACCAAAGTGTT__GATTACAGGCGTGAGCCACTGCACCTGACTG TAA T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1555716228 Functional Loss DEL dbSNP153 33..34 33 - - - 41030 RMVar_ID_41030 Human_SNP_ID_630979280 A-to-I Human chr17 + 68209855 68209855 68209855 GTTGGCCAGGCTGGTCTTGAACTCATAAACTCAGGTGATCCACCCCCTTTGGCCCCCCAAAATGC GTTGGCCAGGCTGGTCTTGAACTCATAAACTCGGGTGATCCACCCCCTTTGGCCCCCCAAAATGC A G lnc-AMZ2-5,lnc-AMZ2-5:2 RNACentral:URS00008C2F0F,RNACentral:URS00008C29FF lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1181486168 Functional Loss SNV dbSNP153 33..33 33 - - - 41031 RMVar_ID_41031 Human_SNP_ID_630980241 A-to-I Human chr17 + 68212696 68212696 68212696 TCAAGCGATACTCCCACCTCAGCCTACCAAGTAGCTAGGATTATACAGGTGCACACCACCACACC TCAAGCGATACTCCCACCTCAGCCTACCAAGTGGCTAGGATTATACAGGTGCACACCACCACACC A G lnc-AMZ2-5,lnc-AMZ2-5:2 RNACentral:URS00008C2F0F,RNACentral:URS00008C29FF lincRNA,lincRNA exon,intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1399709963 Functional Loss SNV dbSNP153 33..33 33 - - - 41032 RMVar_ID_41032 Human_SNP_ID_630981044 A-to-I Human chr17 + 68216227 68216172 68216228 ATGATCATGGCTCACTGCAGCCTCAATCTCCCAGGCTCAGGCTGTCCTCTCACCTCAGCCCCCCT __________________________________GCTCAGGCTGTCCTCTCACCTCAGCCCCCCT CGCCCAGGCTAGAGTGCAGTGGCATGATCATGGCTCACTGCAGCCTCAATCTCCCAG C lnc-AMZ2-5 RNACentral:URS00008C29FF lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1568343946 Functional Loss DEL dbSNP153 1..34 33 - - - 41033 RMVar_ID_41033 Human_SNP_ID_630988140 A-to-I Human chr17 + 68246293 68246293 68246293 TGTAGACTGAGGCACGAGAATCGCTTGAACCCAGGAAGCATAAGTTGCAGTGAGCCGAGATCGCA TGTAGACTGAGGCACGAGAATCGCTTGAACCCGGGAAGCATAAGTTGCAGTGAGCCGAGATCGCA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1555735436 Functional Loss SNV dbSNP153 33..33 33 - - - 41034 RMVar_ID_41034 Human_SNP_ID_630996208 A-to-I Human chr17 - 68278312 68278312 68278312 TTAACTTTTTCTTTCAGATTAAGAATGACCCAAAATAAATTAAAGCTTTGTTCCAAAGCCAATGT TTAACTTTTTCTTTCAGATTAAGAATGACCCATAATAAATTAAAGCTTTGTTCCAAAGCCAATGT T A SLC16A6 Ensembl:ENSG00000108932 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs782457967 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1858210,Human_Splice_Rec_1858220,Human_Splice_Rec_1858238,Human_Splice_Rec_1858248 RMVar_hsa_circ_96538,RMVar_hsa_circ_186783 41035 RMVar_ID_41035 Human_SNP_ID_631002651 A-to-I Human chr17 + 68304719 68304719 68304719 TGTTGTTAATTTTAGATTTAAAAAATACAGATAAGGTCTCACTATGTTGGACAGGCTGATCTTGA TGTTGTTAATTTTAGATTTAAAAAATACAGATCAGGTCTCACTATGTTGGACAGGCTGATCTTGA A C ARSG Ensembl:ENSG00000141337 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1471415099 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106674,RMVar_hsa_circ_186781 41036 RMVar_ID_41036 Human_SNP_ID_631002995 A-to-I Human chr17 + 68306182 68306182 68306182 ACGCCACCATGCCCGGCTCATTTTGTATTTTTAGTAGAACTGGGGTTTCTCCATGTTGGTCAGGC ACGCCACCATGCCCGGCTCATTTTGTATTTTTGGTAGAACTGGGGTTTCTCCATGTTGGTCAGGC A G ARSG Ensembl:ENSG00000141337 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1419424504 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106674,RMVar_hsa_circ_186781 41037 RMVar_ID_41037 Human_SNP_ID_631004581 A-to-I Human chr17 + 68312034 68312034 68312034 GTTGGCTAGGCTACTCTCGAACCCCTGACCTCAAGTGATCCACTCGCCTTGGCCTCCCAAAGTGC GTTGGCTAGGCTACTCTCGAACCCCTGACCTCTAGTGATCCACTCGCCTTGGCCTCCCAAAGTGC A T ARSG Ensembl:ENSG00000141337 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1385489014 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12656,RMVar_hsa_circ_106674,RMVar_hsa_circ_186781,RMVar_hsa_circ_315678,RMVar_hsa_circ_336812,RMVar_hsa_circ_338671,RMVar_hsa_circ_357990,RMVar_hsa_circ_317644,RMVar_hsa_circ_277798,RMVar_hsa_circ_286038,RMVar_hsa_circ_186786,RMVar_hsa_circ_186787,RMVar_hsa_circ_186785 41038 RMVar_ID_41038 Human_SNP_ID_631004961 A-to-I Human chr17 + 68313580 68313580 68313580 CATCTTAACTTAATGACATCTGCGAAGACGCTATCTCCAAATAAGGTCACGTCACAGGTTCTGGA CATCTTAACTTAATGACATCTGCGAAGACGCTGTCTCCAAATAAGGTCACGTCACAGGTTCTGGA A G ARSG Ensembl:ENSG00000141337 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs551294851 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12656,RMVar_hsa_circ_106674,RMVar_hsa_circ_186781,RMVar_hsa_circ_315678,RMVar_hsa_circ_336812,RMVar_hsa_circ_338671,RMVar_hsa_circ_357990,RMVar_hsa_circ_317644,RMVar_hsa_circ_277798,RMVar_hsa_circ_286038,RMVar_hsa_circ_186786,RMVar_hsa_circ_186787,RMVar_hsa_circ_186785 41039 RMVar_ID_41039 Human_SNP_ID_631021676 A-to-I Human chr17 + 68380290 68380290 68380290 TTTTTGGACAGTCTTGCTGTGTTGCCCAGGCTAGAGGGCAGTGATCTAATCAGAGCTCACTGCTG TTTTTGGACAGTCTTGCTGTGTTGCCCAGGCTGGAGGGCAGTGATCTAATCAGAGCTCACTGCTG A G ARSG Ensembl:ENSG00000141337 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs907649078 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20291201,Human_RBP_ID_25337286 RMVar_hsa_circ_15194,RMVar_hsa_circ_12656,RMVar_hsa_circ_315678,RMVar_hsa_circ_338671,RMVar_hsa_circ_357990,RMVar_hsa_circ_277798,RMVar_hsa_circ_34384,RMVar_hsa_circ_110497,RMVar_hsa_circ_328941,RMVar_hsa_circ_186785,RMVar_hsa_circ_76626,RMVar_hsa_circ_40583,RMVar_hsa_circ_113307,RMVar_hsa_circ_186789,RMVar_hsa_circ_186790,RMVar_hsa_circ_365440,RMVar_hsa_circ_373546,RMVar_hsa_circ_186791,RMVar_hsa_circ_327122,RMVar_hsa_circ_69957,RMVar_hsa_circ_186792 41040 RMVar_ID_41040 Human_SNP_ID_631025476 A-to-I Human chr17 + 68396309 68396309 68396309 AAAGTGCTGGGATTACAGGTGTGAGCCACTGTATCCGACCTGCAGCCTGTTCTTGACCAAGCAGA AAAGTGCTGGGATTACAGGTGTGAGCCACTGTTTCCGACCTGCAGCCTGTTCTTGACCAAGCAGA A T ARSG Ensembl:ENSG00000141337 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs920225652 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15194,RMVar_hsa_circ_12656,RMVar_hsa_circ_357990,RMVar_hsa_circ_277798,RMVar_hsa_circ_34384,RMVar_hsa_circ_328941,RMVar_hsa_circ_186785,RMVar_hsa_circ_40583,RMVar_hsa_circ_365440,RMVar_hsa_circ_373546,RMVar_hsa_circ_186792,RMVar_hsa_circ_269229,RMVar_hsa_circ_308988,RMVar_hsa_circ_280118,RMVar_hsa_circ_33625,RMVar_hsa_circ_331923 41041 RMVar_ID_41041 Human_SNP_ID_631032245 A-to-I Human chr17 - 68425246 68425246 68425246 TGAGCTCTGATTGTGCCACTGCACTCCAGCCTAGGTGAAAGAGTGAGACTCTATCTCAAAAAGAA TGAGCTCTGATTGTGCCACTGCACTCCAGCCTGGGTGAAAGAGTGAGACTCTATCTCAAAAAGAA T C WIPI1 Ensembl:ENSG00000070540 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs541830193 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17566158 RMVar_hsa_circ_120345,RMVar_hsa_circ_186794,RMVar_hsa_circ_110301,RMVar_hsa_circ_186793 41042 RMVar_ID_41042 Human_SNP_ID_631032274 A-to-I Human chr17 - 68425342 68425342 68425342 AAAATTAGCCGGGTGTGGTGTCACGTGCCTGTAGTCCCAGCTATTCGGGACGCTGAGATGGGAGG AAAATTAGCCGGGTGTGGTGTCACGTGCCTGTGGTCCCAGCTATTCGGGACGCTGAGATGGGAGG T C WIPI1 Ensembl:ENSG00000070540 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1568619369 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120345,RMVar_hsa_circ_186794,RMVar_hsa_circ_110301,RMVar_hsa_circ_186793 41043 RMVar_ID_41043 Human_SNP_ID_631032340 A-to-I Human chr17 - 68425494 68425494 68425494 ACAAGTGGCCGGGTGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGCTGGAGG ACAAGTGGCCGGGTGCGGTGGCTCACACCTGTTATCCCAGCACTTTGGGAGGCCGAGGCTGGAGG T A WIPI1 Ensembl:ENSG00000070540 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334322976 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120345,RMVar_hsa_circ_186794,RMVar_hsa_circ_110301,RMVar_hsa_circ_186793 41044 RMVar_ID_41044 Human_SNP_ID_631034190 A-to-I Human chr17 + 68432080 68432080 68432080 AAAGAAAATCCTAAAAAGTGGATATAATCTCCAGGGAAAGAGTAAAAAGAACCTCAGGACAAACA AAAGAAAATCCTAAAAAGTGGATATAATCTCCGGGGAAAGAGTAAAAAGAACCTCAGGACAAACA A G AC007780.1 Ensembl:ENSG00000267009 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909438673 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12656 41045 RMVar_ID_41045 Human_SNP_ID_631063960 A-to-I Human chr17 + 68548455 68548455 68548455 GGAAGGCTGAGGCAAGAGAATCGCTTGAACCCAGGAGGCAGAGGTTGCAGCGAGCTGAGATTGAA GGAAGGCTGAGGCAAGAGAATCGCTTGAACCCCGGAGGCAGAGGTTGCAGCGAGCTGAGATTGAA A C PRKAR1A Ensembl:ENSG00000108946 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1007226330 Functional Loss SNV dbSNP153 33..33 33 - - - 41046 RMVar_ID_41046 Human_SNP_ID_631063961 A-to-I Human chr17 + 68548455 68548455 68548455 GGAAGGCTGAGGCAAGAGAATCGCTTGAACCCAGGAGGCAGAGGTTGCAGCGAGCTGAGATTGAA GGAAGGCTGAGGCAAGAGAATCGCTTGAACCCGGGAGGCAGAGGTTGCAGCGAGCTGAGATTGAA A G PRKAR1A Ensembl:ENSG00000108946 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1007226330 Functional Loss SNV dbSNP153 33..33 33 - - - 41047 RMVar_ID_41047 Human_SNP_ID_631234948 A-to-I Human chr17 - 69252592 69252592 69252592 ACCTCAGGTGATCCGCCCCCTTCGGCCTCCCAAACTGCTGGGATTACAGGTGTGAGGCACAGTGC ACCTCAGGTGATCCGCCCCCTTCGGCCTCCCAGACTGCTGGGATTACAGGTGTGAGGCACAGTGC T C ABCA5 Ensembl:ENSG00000154265 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1400711250 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74010,RMVar_hsa_circ_368768,RMVar_hsa_circ_59931 41048 RMVar_ID_41048 Human_SNP_ID_631234979 A-to-I Human chr17 - 69252729 69252729 69252729 AGGCTGAAGCGATTCTCCTGCCTCAGCCTTCCAAGTACCTGGGACTACAGGCAAGAGCCACCAAG AGGCTGAAGCGATTCTCCTGCCTCAGCCTTCCGAGTACCTGGGACTACAGGCAAGAGCCACCAAG T C ABCA5 Ensembl:ENSG00000154265 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1456218184 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74010,RMVar_hsa_circ_368768,RMVar_hsa_circ_59931 41049 RMVar_ID_41049 Human_SNP_ID_631250058 A-to-I Human chr17 - 69309621 69309621 69309621 CCAGGTTGGACTTGAACTTCTGAGCTCAAGCAATCCTCCCATCTTGGTCTTCCAAAATGTTGGGA CCAGGTTGGACTTGAACTTCTGAGCTCAAGCAGTCCTCCCATCTTGGTCTTCCAAAATGTTGGGA T C ABCA5 Ensembl:ENSG00000154265 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017591069 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59931,RMVar_hsa_circ_368471,RMVar_hsa_circ_186839,RMVar_hsa_circ_363665,RMVar_hsa_circ_186849,RMVar_hsa_circ_70660,RMVar_hsa_circ_75436,RMVar_hsa_circ_266452 41050 RMVar_ID_41050 Human_SNP_ID_631250228 A-to-I Human chr17 - 69310300 69310300 69310300 CTCATTTCTACCAAAATTAAAAACAAAAAATTAGCCAGGCATGGTGATGAGTGACTATCGACCAA CTCATTTCTACCAAAATTAAAAACAAAAAATTTGCCAGGCATGGTGATGAGTGACTATCGACCAA T A ABCA5 Ensembl:ENSG00000154265 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs764683312 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59931,RMVar_hsa_circ_368471,RMVar_hsa_circ_186839,RMVar_hsa_circ_363665,RMVar_hsa_circ_186849,RMVar_hsa_circ_70660,RMVar_hsa_circ_75436,RMVar_hsa_circ_266452 41051 RMVar_ID_41051 Human_SNP_ID_631250249 A-to-I Human chr17 - 69310408 69310408 69310408 GTGCAGGTGCACTGGCTCATGCCTGTAATCCCAACTAGTCCGGAGGCTCAGGTGGGAGGATCACT GTGCAGGTGCACTGGCTCATGCCTGTAATCCCCACTAGTCCGGAGGCTCAGGTGGGAGGATCACT T G ABCA5 Ensembl:ENSG00000154265 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs561509153 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59931,RMVar_hsa_circ_368471,RMVar_hsa_circ_186839,RMVar_hsa_circ_363665,RMVar_hsa_circ_186849,RMVar_hsa_circ_70660,RMVar_hsa_circ_75436,RMVar_hsa_circ_266452 41052 RMVar_ID_41052 Human_SNP_ID_631251917 A-to-I Human chr17 - 69317179 69317179 69317179 TTGGCCAAGCTGGTCTCAAACCCCTGACCTCAAGTGATCCACCCGCCTTGGCTTCCCAAAGTGCT TTGGCCAAGCTGGTCTCAAACCCCTGACCTCAGGTGATCCACCCGCCTTGGCTTCCCAAAGTGCT T C ABCA5 Ensembl:ENSG00000154265 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1355278297 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1860308 RMVar_hsa_circ_186839 41053 RMVar_ID_41053 Human_SNP_ID_631251921 A-to-I Human chr17 - 69317193 69317193 69317193 GGGGTTTTGCCATGTTGGCCAAGCTGGTCTCAAACCCCTGACCTCAAGTGATCCACCCGCCTTGG GGGGTTTTGCCATGTTGGCCAAGCTGGTCTCAGACCCCTGACCTCAAGTGATCCACCCGCCTTGG T C ABCA5 Ensembl:ENSG00000154265 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs930663643 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1860308 RMVar_hsa_circ_186839 41054 RMVar_ID_41054 Human_SNP_ID_631251932 A-to-I Human chr17 - 69317231 69317231 69317231 GCCCAGCTAATTTTTGTATATTTTTTTTTAGTAGAGACGGGGTTTTGCCATGTTGGCCAAGCTGG GCCCAGCTAATTTTTGTATATTTTTTTTTAGTGGAGACGGGGTTTTGCCATGTTGGCCAAGCTGG T C ABCA5 Ensembl:ENSG00000154265 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1469801167 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1860308 RMVar_hsa_circ_186839 41055 RMVar_ID_41055 Human_SNP_ID_631251953 A-to-I Human chr17 - 69317281 69317281 69317281 ATTCTGCCTCGGCTTCCTGAGTAGCTGGAGTTACAGGAACGTACCACCATGCCCAGCTAATTTTT ATTCTGCCTCGGCTTCCTGAGTAGCTGGAGTTGCAGGAACGTACCACCATGCCCAGCTAATTTTT T C ABCA5 Ensembl:ENSG00000154265 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs896870812 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_186839 41056 RMVar_ID_41056 Human_SNP_ID_631251971 A-to-I Human chr17 - 69317348 69317348 69317348 ATGCCCAGGCTGGAATGCAGTGGTGCAATCTCAGCTCACTGCAACCTCTGCCTCCCAGATTTAAG ATGCCCAGGCTGGAATGCAGTGGTGCAATCTCGGCTCACTGCAACCTCTGCCTCCCAGATTTAAG T C ABCA5 Ensembl:ENSG00000154265 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1382971704 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_186839 41057 RMVar_ID_41057 Human_SNP_ID_631252213 A-to-I Human chr17 - 69318319 69318319 69318319 AGGCAAAGGCAGATGGATCACCTGAGGTCAGAAGTTTGAGACCAGTCTGACCAACATGGTGAAAT AGGCAAAGGCAGATGGATCACCTGAGGTCAGACGTTTGAGACCAGTCTGACCAACATGGTGAAAT T G ABCA5 Ensembl:ENSG00000154265 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1354867258 Functional Loss SNV dbSNP153 33..33 33 - - - 41058 RMVar_ID_41058 Human_SNP_ID_631253832 A-to-I Human chr17 - 69325226 69325226 69325226 TGGCTCACTGCAGCCTTGACTTCGCAGGCTCAAGTGATCCTCCCACCTCAGCCTCCCAAGTAGCT TGGCTCACTGCAGCCTTGACTTCGCAGGCTCATGTGATCCTCCCACCTCAGCCTCCCAAGTAGCT T A ABCA5 Ensembl:ENSG00000154265 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1467152907 Functional Loss SNV dbSNP153 33..33 33 - - - 41059 RMVar_ID_41059 Human_SNP_ID_631280089 A-to-I Human chr17 + 69435381 69435380 69435381 ATATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCCAGGTGTGGTGGCACATGCCTGT ATATGGTGAAACCCCGTCTCTACTAAAAATAC_AAAATTAGCCAGGTGTGGTGGCACATGCCTGT CA C MAP2K6,AC015920.1 Ensembl:ENSG00000108984,Ensembl:ENSG00000278972 Protein coding,Other intron,exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1429738273 Functional Loss DEL dbSNP153 33..33 33 - - - 41060 RMVar_ID_41060 Human_SNP_ID_631293305 A-to-I Human chr17 + 69493638 69493638 69493638 CAAAAATAAGCTGGGCATGGTGGTGTACGTCTATAGTCCCAGCTACTTGGGAGGCTGAGAAAGGA CAAAAATAAGCTGGGCATGGTGGTGTACGTCTGTAGTCCCAGCTACTTGGGAGGCTGAGAAAGGA A G MAP2K6 Ensembl:ENSG00000108984 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1449951821 Functional Loss SNV dbSNP153 33..33 33 - - - 41061 RMVar_ID_41061 Human_SNP_ID_631828005 A-to-I Human chr17 + 71621409 71621409 71621409 GAGGGCAGCAATGGTTGTATCGACTATGAAGCATTTGTGAGGCATATCCTGTCGGGATGACTGGC GAGGGCAGCAATGGTTGTATCGACTATGAAGCGTTTGTGAGGCATATCCTGTCGGGATGACTGGC A G MYL6P5 Ensembl:ENSG00000228118 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs911590375 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6656342,Human_RBP_ID_8254707 Human_miRNA_ID_1817734,Human_miRNA_ID_1909455 41062 RMVar_ID_41062 Human_SNP_ID_631828033 A-to-I Human chr17 + 71621451 71621451 71621451 CATATCCTGTCGGGATGACTGGCCCATGGGGCAGAGCTCGTCCTTACGGTGCTGAATGGCTGAGG CATATCCTGTCGGGATGACTGGCCCATGGGGCGGAGCTCGTCCTTACGGTGCTGAATGGCTGAGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1010078397 Functional Loss SNV dbSNP153 33..33 33 - - - 41063 RMVar_ID_41063 Human_SNP_ID_632111088 A-to-I Human chr17 - 72728359 72728351 72728360 TGGCTCACTGCACCCTCGACCCCCTGGGCTCAAGCGATCCTCCCACCTCAGCATCCCTCCCAAGC TGGCTCACTGCACCCTCGACCCCCTGGGCTC_________TCCCACCTCAGCATCCCTCCCAAGC AGGATCGCTT A SLC39A11 Ensembl:ENSG00000133195 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1342270587 Functional Loss DEL dbSNP153 32..40 33 - - - RMVar_hsa_circ_107514,RMVar_hsa_circ_186863,RMVar_hsa_circ_62492 41064 RMVar_ID_41064 Human_SNP_ID_632131035 A-to-I Human chr17 - 72804173 72804173 72804173 GCTAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAAAATTAACCAGACGTGGTGGCGGGC GCTAACATGGTGAAACCCCGTCTCTACTAAAATTACAAAAAAATTAACCAGACGTGGTGGCGGGC T A SLC39A11 Ensembl:ENSG00000133195 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs961460791 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107514,RMVar_hsa_circ_186863,RMVar_hsa_circ_319112 41065 RMVar_ID_41065 Human_SNP_ID_632131493 A-to-I Human chr17 - 72805948 72805948 72805948 CAGGAGTTCAAGACCAGCCTGGCCAACCTGGCAAAATCCTGTCTCTACTATAATACAAAAAAAAA CAGGAGTTCAAGACCAGCCTGGCCAACCTGGCGAAATCCTGTCTCTACTATAATACAAAAAAAAA T C SLC39A11 Ensembl:ENSG00000133195 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1408270591 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107514,RMVar_hsa_circ_186863,RMVar_hsa_circ_319112 41066 RMVar_ID_41066 Human_SNP_ID_632139118 A-to-I Human chr17 - 72838064 72838060 72838065 GGCCAGGGTGGCCTCGAACTGCTGGCCTCAAGAGAACCTCCTGCTTCAGCCTCCCATAGTGCTGA GGCCAGGGTGGCCTCGAACTGCTGGCCTCAA_____CCTCCTGCTTCAGCCTCCCATAGTGCTGA GTTCTC G SLC39A11 Ensembl:ENSG00000133195 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1022537740 Functional Loss DEL dbSNP153 32..36 33 - - - Human_Splice_Rec_1861738 RMVar_hsa_circ_107514,RMVar_hsa_circ_186863,RMVar_hsa_circ_319112 41067 RMVar_ID_41067 Human_SNP_ID_632217152 A-to-I Human chr17 - 73129227 73129227 73129227 TTTTTGTATTTTTGTAGAGATGGGGTTTCATCATGTTGGCTGGGCTGGTCTTGAACTTCTGACCT TTTTTGTATTTTTGTAGAGATGGGGTTTCATCGTGTTGGCTGGGCTGGTCTTGAACTTCTGACCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1038589765 Functional Loss SNV dbSNP153 33..33 33 - - - 41068 RMVar_ID_41068 Human_SNP_ID_632229659 A-to-I Human chr17 + 73175547 73175547 73175547 GAACTCTTGACCTCAGGTGATCCGCCTGCCTCAGTGTCCCAAAGTGTTGGGATTACAGGCACGAG GAACTCTTGACCTCAGGTGATCCGCCTGCCTCGGTGTCCCAAAGTGTTGGGATTACAGGCACGAG A G SSTR2,AC097641.1 Ensembl:ENSG00000180616,Ensembl:ENSG00000264860 Protein coding,lincRNA 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1568288192 Functional Loss SNV dbSNP153 33..33 33 - - - 41069 RMVar_ID_41069 Human_SNP_ID_632236450 A-to-I Human chr17 - 73199713 73199713 73199713 ACAATTTGCCAGGCGTCATGGTGCACACCTGTAGTTGCAGCTACTTGGGAGACTGAGGTAGGAGG ACAATTTGCCAGGCGTCATGGTGCACACCTGTGGTTGCAGCTACTTGGGAGACTGAGGTAGGAGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1134883 Functional Loss SNV dbSNP153 33..33 33 - - - 41070 RMVar_ID_41070 Human_SNP_ID_632237954 A-to-I Human chr17 - 73204734 73204734 73204734 TGGGCAAAATCGCAAAACCTGTCTCTACAAAAAATAACAAAAATTAGGTGTGCTGGCGCATGCCT TGGGCAAAATCGCAAAACCTGTCTCTACAAAAGATAACAAAAATTAGGTGTGCTGGCGCATGCCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215260948 Functional Loss SNV dbSNP153 33..33 33 - - - 41071 RMVar_ID_41071 Human_SNP_ID_632238018 A-to-I Human chr17 + 73204998 73204998 73204998 CAGCCTGACCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCCGGGTGTGGTGG CAGCCTGACCAACATGGTGAAACCCCATCTCTGCTAAAAATACAAAAATTAGCCGGGTGTGGTGG A G COG1 Ensembl:ENSG00000166685 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs568606746 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_186873,RMVar_hsa_circ_83710,RMVar_hsa_circ_123303,RMVar_hsa_circ_186875,RMVar_hsa_circ_186872,RMVar_hsa_circ_303833 41072 RMVar_ID_41072 Human_SNP_ID_632238029 A-to-I Human chr17 + 73205042 73205042 73205042 AAAATTAGCCGGGTGTGGTGGCGTACATCTGTAGTCCCAGCTACTCAGGAGGGTGAGGCAGGAGA AAAATTAGCCGGGTGTGGTGGCGTACATCTGTGGTCCCAGCTACTCAGGAGGGTGAGGCAGGAGA A G COG1 Ensembl:ENSG00000166685 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1233482549 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_186873,RMVar_hsa_circ_83710,RMVar_hsa_circ_123303,RMVar_hsa_circ_186875,RMVar_hsa_circ_186872,RMVar_hsa_circ_303833 41073 RMVar_ID_41073 Human_SNP_ID_632238032 A-to-I Human chr17 + 73205056 73205056 73205056 GTGGTGGCGTACATCTGTAGTCCCAGCTACTCAGGAGGGTGAGGCAGGAGAATTGCTTGAACCTG GTGGTGGCGTACATCTGTAGTCCCAGCTACTCCGGAGGGTGAGGCAGGAGAATTGCTTGAACCTG A C COG1 Ensembl:ENSG00000166685 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs757602542 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_186873,RMVar_hsa_circ_83710,RMVar_hsa_circ_123303,RMVar_hsa_circ_186875,RMVar_hsa_circ_186872,RMVar_hsa_circ_303833 41074 RMVar_ID_41074 Human_SNP_ID_632238034 A-to-I Human chr17 + 73205069 73205069 73205069 TCTGTAGTCCCAGCTACTCAGGAGGGTGAGGCAGGAGAATTGCTTGAACCTGGGAGGTGGAGGTT TCTGTAGTCCCAGCTACTCAGGAGGGTGAGGCCGGAGAATTGCTTGAACCTGGGAGGTGGAGGTT A C COG1 Ensembl:ENSG00000166685 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1033955142 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_186873,RMVar_hsa_circ_83710,RMVar_hsa_circ_123303,RMVar_hsa_circ_186875,RMVar_hsa_circ_186872,RMVar_hsa_circ_303833 41075 RMVar_ID_41075 Human_SNP_ID_632238035 A-to-I Human chr17 + 73205069 73205069 73205069 TCTGTAGTCCCAGCTACTCAGGAGGGTGAGGCAGGAGAATTGCTTGAACCTGGGAGGTGGAGGTT TCTGTAGTCCCAGCTACTCAGGAGGGTGAGGCGGGAGAATTGCTTGAACCTGGGAGGTGGAGGTT A G COG1 Ensembl:ENSG00000166685 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1033955142 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_186873,RMVar_hsa_circ_83710,RMVar_hsa_circ_123303,RMVar_hsa_circ_186875,RMVar_hsa_circ_186872,RMVar_hsa_circ_303833 41076 RMVar_ID_41076 Human_SNP_ID_632245232 A-to-I Human chr17 - 73230234 73230234 73230234 TGGAGTGCAGTGGCCCCATCATGCCTCACTGCAGCCTCAACCTCCCAGGCTCAGGTGATCCTCCC TGGAGTGCAGTGGCCCCATCATGCCTCACTGCCGCCTCAACCTCCCAGGCTCAGGTGATCCTCCC T G FAM104A Ensembl:ENSG00000133193 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1430309509 Functional Loss SNV dbSNP153 33..33 33 - - - 41077 RMVar_ID_41077 Human_SNP_ID_632255347 A-to-I Human chr17 - 73266151 73266147 73266151 TTCTTTCTTTCTTTCTGTTGGGACAGAGTCTTACTTTGTCACCCAGGCTGGAGTGCAGTGGTGCA TTCTTTCTTTCTTTCTGTTGGGACAGAGTCTT____TGTCACCCAGGCTGGAGTGCAGTGGTGCA AAAGT A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1396159906 Functional Loss DEL dbSNP153 33..36 33 - - - 41078 RMVar_ID_41078 Human_SNP_ID_632265610 A-to-I Human chr17 - 73302638 73302638 73302638 ACACTTGAGGCTAGGAATTTTAAGACTTGGCTAGGCAACATGGTGGTGCACACCTGTAGTCCCAG ACACTTGAGGCTAGGAATTTTAAGACTTGGCTGGGCAACATGGTGGTGCACACCTGTAGTCCCAG T C CDC42EP4 Ensembl:ENSG00000179604 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167077340 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13154313 41079 RMVar_ID_41079 Human_SNP_ID_632267400 A-to-I Human chr17 - 73308916 73308916 73308916 CTCCTGCCTCAGCCTCTGCAGTAGCTGGGATTATAGGTGCATGCCACCACGCCCGGCTAATTTTT CTCCTGCCTCAGCCTCTGCAGTAGCTGGGATTGTAGGTGCATGCCACCACGCCCGGCTAATTTTT T C CDC42EP4 Ensembl:ENSG00000179604 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432114067 Functional Loss SNV dbSNP153 33..33 33 - - - 41080 RMVar_ID_41080 Human_SNP_ID_632279637 A-to-I Human chr17 - 73353008 73353008 73353008 CAGCTCACTGCAACTTCCATCTCCCAGCTTCAAGCAATTCCCTGCCTCAGCTTCCCCAGTAGCTG CAGCTCACTGCAACTTCCATCTCCCAGCTTCACGCAATTCCCTGCCTCAGCTTCCCCAGTAGCTG T G SDK2 Ensembl:ENSG00000069188 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs917808392 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_340299 41081 RMVar_ID_41081 Human_SNP_ID_632279639 A-to-I Human chr17 - 73353022 73353022 73353022 CAGTGGCGTGATCTCAGCTCACTGCAACTTCCATCTCCCAGCTTCAAGCAATTCCCTGCCTCAGC CAGTGGCGTGATCTCAGCTCACTGCAACTTCCGTCTCCCAGCTTCAAGCAATTCCCTGCCTCAGC T C SDK2 Ensembl:ENSG00000069188 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs978294923 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_340299 41082 RMVar_ID_41082 Human_SNP_ID_632459941 A-to-I Human chr17 - 74052217 74052217 74052217 TATGTCTCTTCCAAAAAAAACAAAAATTATCCAGGTGTGGTGGCGCGTGCCTGTGGTCCCAGCTG TATGTCTCTTCCAAAAAAAACAAAAATTATCCGGGTGTGGTGGCGCGTGCCTGTGGTCCCAGCTG T C LINC02074 Ensembl:ENSG00000266357 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1231511481 Functional Loss SNV dbSNP153 33..33 33 - - - 41083 RMVar_ID_41083 Human_SNP_ID_632499086 A-to-I Human chr17 - 74188604 74188604 74188604 TTGAATACAGATGCAGTTTTGCCACGTTGGCCAGGCTGGTCTAGAACTCCTGACCTCAAGTGATC TTGAATACAGATGCAGTTTTGCCACGTTGGCCCGGCTGGTCTAGAACTCCTGACCTCAAGTGATC T G HSALNG0118631 RNACentral:URS0000EB6B65 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1211422958 Functional Loss SNV dbSNP153 33..33 33 - - - 41084 RMVar_ID_41084 Human_SNP_ID_632503768 A-to-I Human chr17 + 74204874 74204873 74204875 GCCTAGCTGATTTTTGTGTTTTTGGTAGAGACAGAGTTTCACCATGTTGGCCAGGCTGGTCTCGA GCCTAGCTGATTTTTGTGTTTTTGGTAGAGAC__AGTTTCACCATGTTGGCCAGGCTGGTCTCGA CAG C RPL38 Ensembl:ENSG00000172809 Protein coding intron GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs551379115 Functional Loss DEL dbSNP153 33..34 33 - - - 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 41085 RMVar_ID_41085 Human_SNP_ID_632504089 A-to-I Human chr17 + 74205849 74205849 74205849 CAAGACCAACCTGGGCGACATGGCAAAACCCCATTTCTACTAAAAATAAAAAAATTAGCCAGGCA CAAGACCAACCTGGGCGACATGGCAAAACCCCTTTTCTACTAAAAATAAAAAAATTAGCCAGGCA A T RPL38 Ensembl:ENSG00000172809 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1183952694 Functional Loss SNV dbSNP153 33..33 33 - - - 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 41086 RMVar_ID_41086 Human_SNP_ID_632504181 A-to-I Human chr17 + 74206192 74206192 74206192 GCATAGCGTAAAAGTTACCATTTACACTGGGTATGGTGGTTCCCATCTGTAATCCCAGCACTTTG GCATAGCGTAAAAGTTACCATTTACACTGGGTGTGGTGGTTCCCATCTGTAATCCCAGCACTTTG A G RPL38 Ensembl:ENSG00000172809 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs928398337 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13155197 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 41087 RMVar_ID_41087 Human_SNP_ID_632504218 A-to-I Human chr17 + 74206330 74206330 74206330 AGCCGGGCGTGTGCTGGTGGTCCTAGCTACTCAGGAGGCTGAGGTAGGATTGCTTGAATCCAGGA AGCCGGGCGTGTGCTGGTGGTCCTAGCTACTCGGGAGGCTGAGGTAGGATTGCTTGAATCCAGGA A G RPL38 Ensembl:ENSG00000172809 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs565818876 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6642016,Human_RBP_ID_13155206 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 41088 RMVar_ID_41088 Human_SNP_ID_632504496 A-to-I Human chr17 + 74207151 74207151 74207151 CTCCCACCTTAGCCTCCAGAGTCTCTGGGACTACAGGCATGCGCCACCACACCTGGCTAATTTTT CTCCCACCTTAGCCTCCAGAGTCTCTGGGACTGCAGGCATGCGCCACCACACCTGGCTAATTTTT A G RPL38 Ensembl:ENSG00000172809 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs969439476 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13155260 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 41089 RMVar_ID_41089 Human_SNP_ID_632504517 A-to-I Human chr17 + 74207218 74207218 74207218 TGTTTTAGAGATGGATCTGTGTTGGCCAGGCTAGTCTCCAACTCCTGGCCTCAAGCAGTCCTCCC TGTTTTAGAGATGGATCTGTGTTGGCCAGGCTGGTCTCCAACTCCTGGCCTCAAGCAGTCCTCCC A G RPL38 Ensembl:ENSG00000172809 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1473174714 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6642026,Human_RBP_ID_13155264 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 41090 RMVar_ID_41090 Human_SNP_ID_632504662 A-to-I Human chr17 + 74207758 74207758 74207758 GAACTCCCGACCTCAGGTGATCCACCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAA GAACTCCCGACCTCAGGTGATCCACCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAA A G RPL38 Ensembl:ENSG00000172809 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1325344026 Functional Loss SNV dbSNP153 33..33 33 - - - 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 41091 RMVar_ID_41091 Human_SNP_ID_632504913 A-to-I Human chr17 + 74208672 74208672 74208672 TTAAAAAGATAATAGGCCAGGTGCGGTGGCTCATGCCTGGAATCCCAGCACTTTGGGAGGCCGAG TTAAAAAGATAATAGGCCAGGTGCGGTGGCTCGTGCCTGGAATCCCAGCACTTTGGGAGGCCGAG A G RPL38 Ensembl:ENSG00000172809 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1285358110 Functional Loss SNV dbSNP153 33..33 33 - - - 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 41092 RMVar_ID_41092 Human_SNP_ID_632504914 A-to-I Human chr17 + 74208672 74208672 74208672 TTAAAAAGATAATAGGCCAGGTGCGGTGGCTCATGCCTGGAATCCCAGCACTTTGGGAGGCCGAG TTAAAAAGATAATAGGCCAGGTGCGGTGGCTCTTGCCTGGAATCCCAGCACTTTGGGAGGCCGAG A T RPL38 Ensembl:ENSG00000172809 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1285358110 Functional Loss SNV dbSNP153 33..33 33 - - - 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 41093 RMVar_ID_41093 Human_SNP_ID_632577118 A-to-I Human chr17 + 74468432 74468432 74468432 ACGGTTCACTGTAGCCTCCACCTCCCGGGCTCAAGTGATCCTCCCACCTCAACCTCCCCAGTAGC ACGGTTCACTGTAGCCTCCACCTCCCGGGCTCCAGTGATCCTCCCACCTCAACCTCCCCAGTAGC A C CD300A Ensembl:ENSG00000167851 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs985123476 Functional Loss SNV dbSNP153 33..33 33 - - - 41094 RMVar_ID_41094 Human_SNP_ID_632577125 A-to-I Human chr17 + 74468472 74468472 74468472 CTCCCACCTCAACCTCCCCAGTAGCTGAGACTACAGGTGTGTGCCACCACACCCAGCTGGATTCT CTCCCACCTCAACCTCCCCAGTAGCTGAGACTGCAGGTGTGTGCCACCACACCCAGCTGGATTCT A G CD300A Ensembl:ENSG00000167851 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs965626476 Functional Loss SNV dbSNP153 33..33 33 - - - 41095 RMVar_ID_41095 Human_SNP_ID_632656380 A-to-I Human chr17 + 74766654 74766654 74766654 AAATGGCAAACGTAGGCCAGACATTTGCTCACACCTGTAATCCCAACACTTTGGGAGGCCAAGGT AAATGGCAAACGTAGGCCAGACATTTGCTCACGCCTGTAATCCCAACACTTTGGGAGGCCAAGGT A G SLC9A3R1 Ensembl:ENSG00000109062 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs899911330 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17566164 RMVar_hsa_circ_100590,RMVar_hsa_circ_110648,RMVar_hsa_circ_186921,RMVar_hsa_circ_83833,RMVar_hsa_circ_186920,RMVar_hsa_circ_186923 41096 RMVar_ID_41096 Human_SNP_ID_632659918 A-to-I Human chr17 + 74777741 74777741 74777741 CAGGAGTTCAAGACCAGCCTGGCCAACATGGTAAAACCCTGTCTCTACTAAAAATACAAAATTAG CAGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCCTGTCTCTACTAAAAATACAAAATTAG A G TMEM104 Ensembl:ENSG00000109066 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1162942249 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18839,RMVar_hsa_circ_77827,RMVar_hsa_circ_122608,RMVar_hsa_circ_186930,RMVar_hsa_circ_186931,RMVar_hsa_circ_118383,RMVar_hsa_circ_186932 41097 RMVar_ID_41097 Human_SNP_ID_632687821 A-to-I Human chr17 - 74877538 74877538 74877538 GCGAGATCAGGAGCTCGAGACCACCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATACA GCGAGATCAGGAGCTCGAGACCACCCTGGCCACCATGGTGAAACCCCGTCTCTACTAAAAATACA T G FADS6 Ensembl:ENSG00000172782 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1428818036 Functional Loss SNV dbSNP153 33..33 33 - - - 41098 RMVar_ID_41098 Human_SNP_ID_632702947 A-to-I Human chr17 + 74930128 74930128 74930128 TGGCTTGAATCCGGGAGGTGAAGCTTGCAGTGAGCCAAGATCACACCATTGCACTCCAGCCTGAG TGGCTTGAATCCGGGAGGTGAAGCTTGCAGTGGGCCAAGATCACACCATTGCACTCCAGCCTGAG A G OTOP2 Ensembl:ENSG00000183034 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs545562054 Functional Loss SNV dbSNP153 33..33 33 - - - 41099 RMVar_ID_41099 Human_SNP_ID_632722324 A-to-I Human chr17 + 74998452 74998452 74998452 TGAGGGAGGAAGATCGTTGAGCCCAGGAGTTCAAGGCTGCAGCACATATGATCACACCTGTGAAT TGAGGGAGGAAGATCGTTGAGCCCAGGAGTTCGAGGCTGCAGCACATATGATCACACCTGTGAAT A G CDR2L Ensembl:ENSG00000109089 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1239060393 Functional Loss SNV dbSNP153 33..33 33 - - - 41100 RMVar_ID_41100 Human_SNP_ID_353378575 A-to-I Human chr8 - 15083820 15083820 15083820 CAGCAATGAGGTGGGAAGACTGTTTGAGCCCAAGAGCTAGAGACCAGCCTGGGGAACGTAGGGAG CAGCAATGAGGTGGGAAGACTGTTTGAGCCCACGAGCTAGAGACCAGCCTGGGGAACGTAGGGAG T G SGCZ Ensembl:ENSG00000185053 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1171378360 Functional Loss SNV dbSNP153 33..33 33 - - - 41101 RMVar_ID_41101 Human_SNP_ID_353619360 A-to-I Human chr8 + 15754596 15754596 15754596 ACATAACACCTTCTACTTTTTTTCCTTTTCTTAAGAAAAGCACCTTTAGTAATGGCCTTTAGGCT ACATAACACCTTCTACTTTTTTTCCTTTTCTTTAGAAAAGCACCTTTAGTAATGGCCTTTAGGCT A T TUSC3 Ensembl:ENSG00000104723 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs892146373 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7819547 RMVar_hsa_circ_102188,RMVar_hsa_circ_86008,RMVar_hsa_circ_16468,RMVar_hsa_circ_250315,RMVar_hsa_circ_250316 41102 RMVar_ID_41102 Human_SNP_ID_354058552 A-to-I Human chr8 + 17031539 17031539 17031539 TCAAACTCCTGACCTCAAGTTCCGCCTGCCTCAGCTTGCAAAGTGCTGGGAATACAGTCGTGAGC TCAAACTCCTGACCTCAAGTTCCGCCTGCCTCCGCTTGCAAAGTGCTGGGAATACAGTCGTGAGC A C MICU3 Ensembl:ENSG00000155970 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1158213111 Functional Loss SNV dbSNP153 33..33 33 - - - 41103 RMVar_ID_41103 Human_SNP_ID_354123528 A-to-I Human chr8 - 17240310 17240310 17240310 TTTTAAGAAAGTTGACAAATTTGTATTGGGCTACATTCACAGCCATGCCGGGCCACATGTGGCCC TTTTAAGAAAGTTGACAAATTTGTATTGGGCTGCATTCACAGCCATGCCGGGCCACATGTGGCCC T C CNOT7 Ensembl:ENSG00000198791 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1047779164 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17578575 RMVar_hsa_circ_24217,RMVar_hsa_circ_124976,RMVar_hsa_circ_250374,RMVar_hsa_circ_2513,RMVar_hsa_circ_366190 41104 RMVar_ID_41104 Human_SNP_ID_354123533 A-to-I Human chr8 - 17240318 17240318 17240318 TCAAAATGTTTTAAGAAAGTTGACAAATTTGTATTGGGCTACATTCACAGCCATGCCGGGCCACA TCAAAATGTTTTAAGAAAGTTGACAAATTTGTTTTGGGCTACATTCACAGCCATGCCGGGCCACA T A CNOT7 Ensembl:ENSG00000198791 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs558574616 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17578575 RMVar_hsa_circ_24217,RMVar_hsa_circ_124976,RMVar_hsa_circ_250374,RMVar_hsa_circ_2513,RMVar_hsa_circ_366190 41105 RMVar_ID_41105 Human_SNP_ID_354123749 A-to-I Human chr8 - 17240924 17240924 17240924 TGAGATTTTTTTGTTGTTGTTTAAGTTAGTTTATTTAATGTGTGGCCCAAGACAGTTCTTTGAGT TGAGATTTTTTTGTTGTTGTTTAAGTTAGTTTGTTTAATGTGTGGCCCAAGACAGTTCTTTGAGT T C CNOT7 Ensembl:ENSG00000198791 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1489298999 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24217,RMVar_hsa_circ_124976,RMVar_hsa_circ_250374,RMVar_hsa_circ_2513,RMVar_hsa_circ_366190 41106 RMVar_ID_41106 Human_SNP_ID_354123782 A-to-I Human chr8 - 17241010 17241010 17241010 CTTGTAAAGTAAACTTGTCCAACCCTTGGCCCAGGATGGCTTTGAATGCAGCCCAACAGAAATTC CTTGTAAAGTAAACTTGTCCAACCCTTGGCCCTGGATGGCTTTGAATGCAGCCCAACAGAAATTC T A CNOT7 Ensembl:ENSG00000198791 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs563574842 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24217,RMVar_hsa_circ_124976,RMVar_hsa_circ_250374,RMVar_hsa_circ_2513,RMVar_hsa_circ_366190 41107 RMVar_ID_41107 Human_SNP_ID_354123783 A-to-I Human chr8 - 17241010 17241010 17241010 CTTGTAAAGTAAACTTGTCCAACCCTTGGCCCAGGATGGCTTTGAATGCAGCCCAACAGAAATTC CTTGTAAAGTAAACTTGTCCAACCCTTGGCCCGGGATGGCTTTGAATGCAGCCCAACAGAAATTC T C CNOT7 Ensembl:ENSG00000198791 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs563574842 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24217,RMVar_hsa_circ_124976,RMVar_hsa_circ_250374,RMVar_hsa_circ_2513,RMVar_hsa_circ_366190 41108 RMVar_ID_41108 Human_SNP_ID_354140665 A-to-I Human chr8 + 17289031 17289031 17289031 GGCTGCATAAATGTCTTCTTATGAAACTGTTCATATCCTTAGCCCACTTTTTGATAGGGTTGTAT GGCTGCATAAATGTCTTCTTATGAAACTGTTCGTATCCTTAGCCCACTTTTTGATAGGGTTGTAT A G VPS37A Ensembl:ENSG00000155975 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1416795150 Functional Loss SNV dbSNP153 33..33 33 - - - 41109 RMVar_ID_41109 Human_SNP_ID_354175495 A-to-I Human chr8 - 17395232 17395232 17395232 CCTTGAAAAGGAATGAAGTTCTGATACATGCTACAATATGGGTGAACCTTGAAGACATTGAAGAC CCTTGAAAAGGAATGAAGTTCTGATACATGCTCCAATATGGGTGAACCTTGAAGACATTGAAGAC T G MTMR7 Ensembl:ENSG00000003987 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs561515251 Functional Loss SNV dbSNP153 33..33 33 - - - 41110 RMVar_ID_41110 Human_SNP_ID_354276891 A-to-I Human chr8 - 17680207 17680207 17680207 CACCTGCCTCGGCCTTCCAAAGTGCTGGGATTACAGGCATGATCCACCACTCCCAGTCCAGAACC CACCTGCCTCGGCCTTCCAAAGTGCTGGGATTGCAGGCATGATCCACCACTCCCAGTCCAGAACC T C MTUS1 Ensembl:ENSG00000129422 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs547769838 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110290,RMVar_hsa_circ_269307,RMVar_hsa_circ_355319,RMVar_hsa_circ_366028,RMVar_hsa_circ_350148,RMVar_hsa_circ_62952,RMVar_hsa_circ_285042,RMVar_hsa_circ_65722,RMVar_hsa_circ_250418,RMVar_hsa_circ_331197,RMVar_hsa_circ_343206,RMVar_hsa_circ_318393,RMVar_hsa_circ_250420,RMVar_hsa_circ_250421,RMVar_hsa_circ_250419 41111 RMVar_ID_41111 Human_SNP_ID_354277247 A-to-I Human chr8 - 17680988 17680988 17680988 TGGAGGTGGCAGTGAGCCAAGATCGCACCACTACACTCCATCCTGGGCAACAGAGCGAGATTCCA TGGAGGTGGCAGTGAGCCAAGATCGCACCACTGCACTCCATCCTGGGCAACAGAGCGAGATTCCA T C MTUS1 Ensembl:ENSG00000129422 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1177976857 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110290,RMVar_hsa_circ_269307,RMVar_hsa_circ_355319,RMVar_hsa_circ_366028,RMVar_hsa_circ_350148,RMVar_hsa_circ_62952,RMVar_hsa_circ_285042,RMVar_hsa_circ_65722,RMVar_hsa_circ_250418,RMVar_hsa_circ_331197,RMVar_hsa_circ_343206,RMVar_hsa_circ_318393,RMVar_hsa_circ_250420,RMVar_hsa_circ_250421,RMVar_hsa_circ_250419 41112 RMVar_ID_41112 Human_SNP_ID_354277289 A-to-I Human chr8 - 17681072 17681072 17681072 AAAATTAGCCATGTGTGGTGGCATGTGCCTGTAGTCCCAGCTACTCGGGAGGCTAAGGTAGAAGA AAAATTAGCCATGTGTGGTGGCATGTGCCTGTTGTCCCAGCTACTCGGGAGGCTAAGGTAGAAGA T A MTUS1 Ensembl:ENSG00000129422 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1376042569 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110290,RMVar_hsa_circ_269307,RMVar_hsa_circ_355319,RMVar_hsa_circ_366028,RMVar_hsa_circ_350148,RMVar_hsa_circ_62952,RMVar_hsa_circ_285042,RMVar_hsa_circ_65722,RMVar_hsa_circ_250418,RMVar_hsa_circ_331197,RMVar_hsa_circ_343206,RMVar_hsa_circ_318393,RMVar_hsa_circ_250420,RMVar_hsa_circ_250421,RMVar_hsa_circ_250419 41113 RMVar_ID_41113 Human_SNP_ID_354277490 A-to-I Human chr8 - 17681651 17681651 17681651 GGAGGAGAAGCAAGAGGGATTTATTGAATACTAGGTTTGAGCAAAAGTAATTGCGGTTTTGCCAT GGAGGAGAAGCAAGAGGGATTTATTGAATACTGGGTTTGAGCAAAAGTAATTGCGGTTTTGCCAT T C MTUS1,MIR548V Ensembl:ENSG00000129422,Ensembl:ENSG00000265520 Protein coding,miRNA intron,exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs936803416 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16505437 Human_miRNA_ID_3135438 RMVar_hsa_circ_110290,RMVar_hsa_circ_269307,RMVar_hsa_circ_355319,RMVar_hsa_circ_366028,RMVar_hsa_circ_350148,RMVar_hsa_circ_62952,RMVar_hsa_circ_285042,RMVar_hsa_circ_65722,RMVar_hsa_circ_250418,RMVar_hsa_circ_331197,RMVar_hsa_circ_343206,RMVar_hsa_circ_318393,RMVar_hsa_circ_250420,RMVar_hsa_circ_250421,RMVar_hsa_circ_250419 41114 RMVar_ID_41114 Human_SNP_ID_354316772 A-to-I Human chr8 - 17789197 17789197 17789197 AGAAACCCTGTATCTACTAAAATTACAAAAGTAGCCAGGTGAGGTGGCTCATTCCTGTAATCCTA AGAAACCCTGTATCTACTAAAATTACAAAAGTTGCCAGGTGAGGTGGCTCATTCCTGTAATCCTA T A MTUS1 Ensembl:ENSG00000129422 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053647641 Functional Loss SNV dbSNP153 33..33 33 - - - 41115 RMVar_ID_41115 Human_SNP_ID_354366148 A-to-I Human chr8 + 17925647 17925647 17925647 TGACGAGGTCAGGAGATCAAGACCATCCGGCTAACATGGTGAAACCCCATCTCTACTAAAAATAC TGACGAGGTCAGGAGATCAAGACCATCCGGCTGACATGGTGAAACCCCATCTCTACTAAAAATAC A G PCM1 Ensembl:ENSG00000078674 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1035315789 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37112,RMVar_hsa_circ_110654,RMVar_hsa_circ_352455,RMVar_hsa_circ_370986,RMVar_hsa_circ_68007,RMVar_hsa_circ_72496,RMVar_hsa_circ_54515,RMVar_hsa_circ_250430,RMVar_hsa_circ_21170,RMVar_hsa_circ_29365,RMVar_hsa_circ_250429 41116 RMVar_ID_41116 Human_SNP_ID_354366149 A-to-I Human chr8 + 17925650 17925650 17925650 CGAGGTCAGGAGATCAAGACCATCCGGCTAACATGGTGAAACCCCATCTCTACTAAAAATACAAA CGAGGTCAGGAGATCAAGACCATCCGGCTAACGTGGTGAAACCCCATCTCTACTAAAAATACAAA A G PCM1 Ensembl:ENSG00000078674 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs144805026 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37112,RMVar_hsa_circ_110654,RMVar_hsa_circ_352455,RMVar_hsa_circ_370986,RMVar_hsa_circ_68007,RMVar_hsa_circ_72496,RMVar_hsa_circ_54515,RMVar_hsa_circ_250430,RMVar_hsa_circ_21170,RMVar_hsa_circ_29365,RMVar_hsa_circ_250429 41117 RMVar_ID_41117 Human_SNP_ID_354418958 A-to-I Human chr8 - 18071015 18071015 18071015 TTAGTAGAGACAAGATTTTGCCATGTTGTCCAAGCTGATCTCAAACTCCTGACCTCGAGTGATCC TTAGTAGAGACAAGATTTTGCCATGTTGTCCAGGCTGATCTCAAACTCCTGACCTCGAGTGATCC T C ASAH1 Ensembl:ENSG00000104763 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1307944686 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_715,RMVar_hsa_circ_88786,RMVar_hsa_circ_250485,RMVar_hsa_circ_57486,RMVar_hsa_circ_280638,RMVar_hsa_circ_312786,RMVar_hsa_circ_317761,RMVar_hsa_circ_250486 41118 RMVar_ID_41118 Human_SNP_ID_354423608 A-to-I Human chr8 - 18084568 18084563 18084568 TCCCTGACTCCGCGGTGGGGATGAATAACTCAACTCATTTCGGGCCGCTTTTCTCAGAGGGCAAA TCCCTGACTCCGCGGTGGGGATGAATAACTCA_____TTTCGGGCCGCTTTTCTCAGAGGGCAAA ATGAGT A ASAH1 Ensembl:ENSG00000104763 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1197578907 Functional Loss DEL dbSNP153 33..37 33 - - - 41119 RMVar_ID_41119 Human_SNP_ID_354426650 A-to-I Human chr8 + 18094727 18094727 18094727 ACAAACATTTTGTCTCTAAAAATACAAAAATTAGCTGGGCATGGTGGCACACACCTGTAGTCCCA ACAAACATTTTGTCTCTAAAAATACAAAAATTGGCTGGGCATGGTGGCACACACCTGTAGTCCCA A G AC124242.1 Ensembl:ENSG00000245281 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs901252968 Functional Loss SNV dbSNP153 33..33 33 - - - 41120 RMVar_ID_41120 Human_SNP_ID_354694859 A-to-I Human chr8 - 18951215 18951215 18951215 ATTTTTTAAATTTTTTGTGGAGATGGTGTCTCACTATGTTGCCCAGGCTGGTCTTGAACTCCTGG ATTTTTTAAATTTTTTGTGGAGATGGTGTCTCGCTATGTTGCCCAGGCTGGTCTTGAACTCCTGG T C PSD3 Ensembl:ENSG00000156011 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1162923327 Functional Loss SNV dbSNP153 33..33 33 - - - 41121 RMVar_ID_41121 Human_SNP_ID_354821068 A-to-I Human chr8 + 19362690 19362690 19362690 TGAACCAGGGAGGCGGAGGTTGCAGTGAGCCGAGATCGTACCACTGCACTTCAGCCTGGGCAATG TGAACCAGGGAGGCGGAGGTTGCAGTGAGCCGGGATCGTACCACTGCACTTCAGCCTGGGCAATG A G SH2D4A Ensembl:ENSG00000104611 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1343242396 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76118,RMVar_hsa_circ_107281,RMVar_hsa_circ_127659,RMVar_hsa_circ_250525,RMVar_hsa_circ_250526,RMVar_hsa_circ_57089,RMVar_hsa_circ_351287,RMVar_hsa_circ_250528,RMVar_hsa_circ_364094,RMVar_hsa_circ_59355,RMVar_hsa_circ_346934,RMVar_hsa_circ_250530 41122 RMVar_ID_41122 Human_SNP_ID_354834149 A-to-I Human chr8 + 19403477 19403477 19403477 GAGCACAGAAAAAAGTATATATATTTGAGACCAGGTCTCACTCTGTTACCCAGGCTGGAGTGCAG GAGCACAGAAAAAAGTATATATATTTGAGACCGGGTCTCACTCTGTTACCCAGGCTGGAGTGCAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903719327 Functional Loss SNV dbSNP153 33..33 33 - - - 41123 RMVar_ID_41123 Human_SNP_ID_354894655 A-to-I Human chr8 - 19576473 19576473 19576473 AAGATTAGGAATAGGCCGGGTGCAATGGCTCAAGCTTGTAATCCTAGCACTCTGAGAGGCTGAGG AAGATTAGGAATAGGCCGGGTGCAATGGCTCAGGCTTGTAATCCTAGCACTCTGAGAGGCTGAGG T C CSGALNACT1 Ensembl:ENSG00000147408 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1013610389 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5576,RMVar_hsa_circ_53361,RMVar_hsa_circ_294294,RMVar_hsa_circ_250538,RMVar_hsa_circ_327765 41124 RMVar_ID_41124 Human_SNP_ID_354899962 A-to-I Human chr8 - 19592654 19592654 19592654 TGCCTTCCAGGCTCATGAGATCCTCCCACCCTAGCCTCCTAAGTAGCTGGGACAGCAGGTGTGTA TGCCTTCCAGGCTCATGAGATCCTCCCACCCTGGCCTCCTAAGTAGCTGGGACAGCAGGTGTGTA T C CSGALNACT1 Ensembl:ENSG00000147408 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1421867109 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5576,RMVar_hsa_circ_53361,RMVar_hsa_circ_294294,RMVar_hsa_circ_250538,RMVar_hsa_circ_37039,RMVar_hsa_circ_45837,RMVar_hsa_circ_327765,RMVar_hsa_circ_287508,RMVar_hsa_circ_250540,RMVar_hsa_circ_360544 41125 RMVar_ID_41125 Human_SNP_ID_354921059 A-to-I Human chr8 - 19653537 19653537 19653537 CATACCTCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGCACCTGGCCGCAGCTG CATACCTCTTGGCCTCCCAAAGTGCTGGGATTGCAGGCATGAGCCACTGCACCTGGCCGCAGCTG T C CSGALNACT1 Ensembl:ENSG00000147408 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432928634 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45837,RMVar_hsa_circ_340519 41126 RMVar_ID_41126 Human_SNP_ID_354977889 A-to-I Human chr8 + 19840935 19840935 19840935 TAATGACATGTTCAACTTGGTAATGCTAAGTTAGTTTCCAGAGTGGCTGCATGACTTTATATACC TAATGACATGTTCAACTTGGTAATGCTAAGTTGGTTTCCAGAGTGGCTGCATGACTTTATATACC A G INTS10 Ensembl:ENSG00000104613 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1403761798 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95876,RMVar_hsa_circ_44149,RMVar_hsa_circ_43432,RMVar_hsa_circ_364148,RMVar_hsa_circ_316230,RMVar_hsa_circ_53253,RMVar_hsa_circ_46349,RMVar_hsa_circ_250555,RMVar_hsa_circ_320990,RMVar_hsa_circ_333353,RMVar_hsa_circ_21549,RMVar_hsa_circ_7742,RMVar_hsa_circ_33642,RMVar_hsa_circ_250567,RMVar_hsa_circ_250568,RMVar_hsa_circ_299428,RMVar_hsa_circ_250571,RMVar_hsa_circ_250574,RMVar_hsa_circ_90857,RMVar_hsa_circ_250576,RMVar_hsa_circ_34646 41127 RMVar_ID_41127 Human_SNP_ID_355600967 A-to-I Human chr8 + 21958675 21958675 21958675 TGTTTAGTGTGAAAGCTGAAACAAGGCAAAGCAAGGCCGGGCATGGTTGCGCATGCCTATAATCC TGTTTAGTGTGAAAGCTGAAACAAGGCAAAGCCAGGCCGGGCATGGTTGCGCATGCCTATAATCC A C XPO7 Ensembl:ENSG00000130227 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985321651 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_250593,RMVar_hsa_circ_119137,RMVar_hsa_circ_83927,RMVar_hsa_circ_93972,RMVar_hsa_circ_250594,RMVar_hsa_circ_250595 41128 RMVar_ID_41128 Human_SNP_ID_355610864 A-to-I Human chr8 + 21995878 21995878 21995878 TTGCTGTCTCCCAGGCTGGAGTGCAGTGGCACAGTCTCGGCTCACTGCAAGCTCCATCCCCCTGG TTGCTGTCTCCCAGGCTGGAGTGCAGTGGCACGGTCTCGGCTCACTGCAAGCTCCATCCCCCTGG A G XPO7 Ensembl:ENSG00000130227 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs569466564 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5827,RMVar_hsa_circ_250593,RMVar_hsa_circ_83927,RMVar_hsa_circ_93972,RMVar_hsa_circ_250594,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_250614,RMVar_hsa_circ_44806,RMVar_hsa_circ_361382,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_250650,RMVar_hsa_circ_111443,RMVar_hsa_circ_250652,RMVar_hsa_circ_75640,RMVar_hsa_circ_250651,RMVar_hsa_circ_118909,RMVar_hsa_circ_250649,RMVar_hsa_circ_102498,RMVar_hsa_circ_108852,RMVar_hsa_circ_250655,RMVar_hsa_circ_250656,RMVar_hsa_circ_308957,RMVar_hsa_circ_250658 41129 RMVar_ID_41129 Human_SNP_ID_355610890 A-to-I Human chr8 + 21995955 21995955 21995955 CCCCTGCCTCAGCCTCCGGAGTAGCTGGGACTACAGGCACCCGCCACCACACCCGGCCGATTTTT CCCCTGCCTCAGCCTCCGGAGTAGCTGGGACTGCAGGCACCCGCCACCACACCCGGCCGATTTTT A G XPO7 Ensembl:ENSG00000130227 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1287062938 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5827,RMVar_hsa_circ_250593,RMVar_hsa_circ_83927,RMVar_hsa_circ_93972,RMVar_hsa_circ_250594,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_250614,RMVar_hsa_circ_44806,RMVar_hsa_circ_361382,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_250650,RMVar_hsa_circ_111443,RMVar_hsa_circ_250652,RMVar_hsa_circ_75640,RMVar_hsa_circ_250651,RMVar_hsa_circ_118909,RMVar_hsa_circ_250649,RMVar_hsa_circ_102498,RMVar_hsa_circ_108852,RMVar_hsa_circ_250655,RMVar_hsa_circ_250656,RMVar_hsa_circ_308957,RMVar_hsa_circ_250658 41130 RMVar_ID_41130 Human_SNP_ID_355611154 A-to-I Human chr8 + 21996926 21996926 21996926 CGCCTCCTGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCACATAGCTGGGATTACAGACATGCG CGCCTCCTGGGTTCAAGCGATTCTCCTGCCTCGGCCTCCCACATAGCTGGGATTACAGACATGCG A G XPO7 Ensembl:ENSG00000130227 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1266061595 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5827,RMVar_hsa_circ_250593,RMVar_hsa_circ_83927,RMVar_hsa_circ_93972,RMVar_hsa_circ_250594,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_250614,RMVar_hsa_circ_44806,RMVar_hsa_circ_361382,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_250650,RMVar_hsa_circ_111443,RMVar_hsa_circ_250652,RMVar_hsa_circ_75640,RMVar_hsa_circ_250651,RMVar_hsa_circ_118909,RMVar_hsa_circ_250649,RMVar_hsa_circ_102498,RMVar_hsa_circ_108852,RMVar_hsa_circ_250655,RMVar_hsa_circ_250656,RMVar_hsa_circ_308957,RMVar_hsa_circ_250658 41131 RMVar_ID_41131 Human_SNP_ID_355621683 A-to-I Human chr8 + 22034946 22034946 22034946 CCTGGTCAACATGATGAAACCCTGTCTCTACTAAAAACACAAAAATTAACCGAGCCTGGTGGCAT CCTGGTCAACATGATGAAACCCTGTCTCTACTGAAAACACAAAAATTAACCGAGCCTGGTGGCAT A G NPM2 Ensembl:ENSG00000158806 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1040302040 Functional Loss SNV dbSNP153 33..33 33 - - - 41132 RMVar_ID_41132 Human_SNP_ID_355621803 A-to-I Human chr8 + 22035391 22035391 22035391 AGCTTCCTGGGCTCAAGCAATCCTCCCACCTCAGCTTTCCAAGTAGCTAGGACTATAGGCACGTG AGCTTCCTGGGCTCAAGCAATCCTCCCACCTCTGCTTTCCAAGTAGCTAGGACTATAGGCACGTG A T NPM2 Ensembl:ENSG00000158806 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1034288574 Functional Loss SNV dbSNP153 33..33 33 - - - 41133 RMVar_ID_41133 Human_SNP_ID_355639815 A-to-I Human chr8 + 22092449 22092449 22092449 TAAAAATACAAAAATCAGCCAGGCGTGGTGGCACATGTCTGTAATCCCAGCAACTTGGGAGGCAG TAAAAATACAAAAATCAGCCAGGCGTGGTGGCCCATGTCTGTAATCCCAGCAACTTGGGAGGCAG A C FAM160B2 Ensembl:ENSG00000158863 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1007063231 Functional Loss SNV dbSNP153 33..33 33 - - - 41134 RMVar_ID_41134 Human_SNP_ID_355644445 A-to-I Human chr8 - 22105336 22105336 22105336 CAGGCTGGAGTGGAGTGGTGTGATCCTGGCTCACTGCAGCCTTGACCTCCCAGGCTCAAGTGACA CAGGCTGGAGTGGAGTGGTGTGATCCTGGCTCGCTGCAGCCTTGACCTCCCAGGCTCAAGTGACA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1380741696 Functional Loss SNV dbSNP153 33..33 33 - - - 41135 RMVar_ID_41135 Human_SNP_ID_355644761 A-to-I Human chr8 - 22106235 22106235 22106235 ATGTTGGCAGATGCCTGTAATCTCAGATACTTAGGAGGCTGAGGCAGGAGAATCGCTTGAACCCC ATGTTGGCAGATGCCTGTAATCTCAGATACTTTGGAGGCTGAGGCAGGAGAATCGCTTGAACCCC T A - - Other Unknown GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs947375991 Functional Loss SNV dbSNP153 33..33 33 - - - 41136 RMVar_ID_41136 Human_SNP_ID_355685176 A-to-I Human chr8 + 22238873 22238873 22238873 CCTGCCTCAGCCTCACAAGTAGCTGGGACTGTAAGTGCACACGACCACACACGGCTAATTTTTTG CCTGCCTCAGCCTCACAAGTAGCTGGGACTGTGAGTGCACACGACCACACACGGCTAATTTTTTG A G RF00017-4572 RNACentral:URS000099187D SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1447119340 Functional Loss SNV dbSNP153 33..33 33 - - - 41137 RMVar_ID_41137 Human_SNP_ID_355686862 A-to-I Human chr8 - 22244082 22244082 22244082 CTTCCACCTCAGCCTCCTGAGTAGCTGGGACTACAAGTGCATGCCACCACGCCCGGCTAATTTTT CTTCCACCTCAGCCTCCTGAGTAGCTGGGACTGCAAGTGCATGCCACCACGCCCGGCTAATTTTT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1195063737 Functional Loss SNV dbSNP153 33..33 33 - - - 41138 RMVar_ID_41138 Human_SNP_ID_355689893 A-to-I Human chr8 + 22253756 22253756 22253756 TGTCGCCCAGTGGTGTGATCTTGGCTTACTGCAACTCTGTCTCCCAGGTTCAAGTGATCCTCCCG TGTCGCCCAGTGGTGTGATCTTGGCTTACTGCTACTCTGTCTCCCAGGTTCAAGTGATCCTCCCG A T POLR3D Ensembl:ENSG00000168495 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946918184 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_697170,Human_RBP_ID_7823669,Human_RBP_ID_8684688,Human_RBP_ID_16392527,Human_RBP_ID_18388856,Human_RBP_ID_26558471 41139 RMVar_ID_41139 Human_SNP_ID_355689940 A-to-I Human chr8 + 22253929 22253906 22253930 AAACTCCTCACCTCAAGTGATCTACCTGCCTCAGCCTCCCAAGTGCTGGGATTACAGGCGTGAGC AAACTCCTCA________________________CCTCCCAAGTGCTGGGATTACAGGCGTGAGC ACCTCAAGTGATCTACCTGCCTCAG A POLR3D Ensembl:ENSG00000168495 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1168686951 Functional Loss DEL dbSNP153 11..34 33 - - - Human_RBP_ID_697173 41140 RMVar_ID_41140 Human_SNP_ID_355689942 A-to-I Human chr8 + 22253929 22253929 22253929 AAACTCCTCACCTCAAGTGATCTACCTGCCTCAGCCTCCCAAGTGCTGGGATTACAGGCGTGAGC AAACTCCTCACCTCAAGTGATCTACCTGCCTCGGCCTCCCAAGTGCTGGGATTACAGGCGTGAGC A G POLR3D Ensembl:ENSG00000168495 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1459177282 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_697173 41141 RMVar_ID_41141 Human_SNP_ID_355690556 A-to-I Human chr8 + 22256396 22256396 22256396 GGCACCCGCTACCAAGCCCAGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCAGGTTGG GGCACCCGCTACCAAGCCCAGCTAATTTTTGTGTTTTTAGTAGAGACAGGGTTTCACCAGGTTGG A G RF00017-4572 RNACentral:URS000099187D SRP RNA intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1348542596 Functional Loss SNV dbSNP153 33..33 33 - - - 41142 RMVar_ID_41142 Human_SNP_ID_355690575 A-to-I Human chr8 + 22256456 22256456 22256456 GTTGGCCAGGCTGGTCTCAAATGCCTAACCTCAGGTGATCCACCCGCCTCGGCCTCCCAAAGTGT GTTGGCCAGGCTGGTCTCAAATGCCTAACCTCGGGTGATCCACCCGCCTCGGCCTCCCAAAGTGT A G RF00017-4572 RNACentral:URS000099187D SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1219081862 Functional Loss SNV dbSNP153 33..33 33 - - - 41143 RMVar_ID_41143 Human_SNP_ID_355690585 A-to-I Human chr8 + 22256483 22256483 22256483 ACCTCAGGTGATCCACCCGCCTCGGCCTCCCAAAGTGTTCGAATTACAGGCGTGAGCCACCACAC ACCTCAGGTGATCCACCCGCCTCGGCCTCCCAGAGTGTTCGAATTACAGGCGTGAGCCACCACAC A G RF00017-4572 RNACentral:URS000099187D SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1563324700 Functional Loss SNV dbSNP153 33..33 33 - - - 41144 RMVar_ID_41144 Human_SNP_ID_355735485 A-to-I Human chr8 - 22412687 22412687 22412687 CACCTGCCTCAGCCTCCCAAAGTGCTGGGAATATAGGTGTGAGCCACTGCACCCGGCTGATGATG CACCTGCCTCAGCCTCCCAAAGTGCTGGGAATGTAGGTGTGAGCCACTGCACCCGGCTGATGATG T C RF00017-4569 RNACentral:URS000090668B SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs997048208 Functional Loss SNV dbSNP153 33..33 33 - - - 41145 RMVar_ID_41145 Human_SNP_ID_355739902 A-to-I Human chr8 + 22429115 22429115 22429115 TAACACGGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTGGCTGGGCGTGGTGGCGGGCACC TAACACGGTGAAACCCCGTCTCTACTAAAAATTCAAAAAATTGGCTGGGCGTGGTGGCGGGCACC A T SLC39A14 Ensembl:ENSG00000104635 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167472121 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_180631 41146 RMVar_ID_41146 Human_SNP_ID_355745946 A-to-I Human chr8 + 22451397 22451397 22451397 ACCTCAGGTGATCTGCCCTCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGTGT ACCTCAGGTGATCTGCCCTCCTCGGCCTCCCAGAGTGCTGGGATTACAGGCGTGAGCCACTGTGT A G PPP3CC Ensembl:ENSG00000120910 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973507994 Functional Loss SNV dbSNP153 33..33 33 - - - 41147 RMVar_ID_41147 Human_SNP_ID_355747530 A-to-I Human chr8 + 22457484 22457478 22457484 ACCACCATGCCCGACTAATTTTTGTGGTTTTTAGTAGAGATAGGGAGGGTTTCACGATGTTGGCC ACCACCATGCCCGACTAATTTTTGTGG______GTAGAGATAGGGAGGGTTTCACGATGTTGGCC GTTTTTA G PPP3CC Ensembl:ENSG00000120910 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1172468680 Functional Loss DEL dbSNP153 28..33 33 - - - 41148 RMVar_ID_41148 Human_SNP_ID_355759472 A-to-I Human chr8 + 22504371 22504371 22504371 TTGTCCAGGCTTGAGTACAATTGTGTAATCATAGCTCACTGCAACTTTGAACTCCTGGGCTTAAG TTGTCCAGGCTTGAGTACAATTGTGTAATCATGGCTCACTGCAACTTTGAACTCCTGGGCTTAAG A G PPP3CC Ensembl:ENSG00000120910 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1448803617 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_250721,RMVar_hsa_circ_20202,RMVar_hsa_circ_271576,RMVar_hsa_circ_324113,RMVar_hsa_circ_311070,RMVar_hsa_circ_102699,RMVar_hsa_circ_271341,RMVar_hsa_circ_56783,RMVar_hsa_circ_250723,RMVar_hsa_circ_250725,RMVar_hsa_circ_250726,RMVar_hsa_circ_250724,RMVar_hsa_circ_250722,RMVar_hsa_circ_39597,RMVar_hsa_circ_316266,RMVar_hsa_circ_88974,RMVar_hsa_circ_250720,RMVar_hsa_circ_359881,RMVar_hsa_circ_250729,RMVar_hsa_circ_325507,RMVar_hsa_circ_283641,RMVar_hsa_circ_304946,RMVar_hsa_circ_50765,RMVar_hsa_circ_250731,RMVar_hsa_circ_250733,RMVar_hsa_circ_250734,RMVar_hsa_circ_250732,RMVar_hsa_circ_250730 41149 RMVar_ID_41149 Human_SNP_ID_355761143 A-to-I Human chr8 + 22511354 22511354 22511354 CTCTTTCACCCGGGCTGAAGTACAGTGGTGCTATCTCAGCTCACTGCAACCTCCGCCTCCCTGGT CTCTTTCACCCGGGCTGAAGTACAGTGGTGCTGTCTCAGCTCACTGCAACCTCCGCCTCCCTGGT A G PPP3CC Ensembl:ENSG00000120910 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1202516506 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_250721,RMVar_hsa_circ_20202,RMVar_hsa_circ_271576,RMVar_hsa_circ_324113,RMVar_hsa_circ_311070,RMVar_hsa_circ_102699,RMVar_hsa_circ_56783,RMVar_hsa_circ_250723,RMVar_hsa_circ_250725,RMVar_hsa_circ_250724,RMVar_hsa_circ_250722,RMVar_hsa_circ_39597,RMVar_hsa_circ_88974,RMVar_hsa_circ_250720,RMVar_hsa_circ_359881,RMVar_hsa_circ_250729,RMVar_hsa_circ_325507,RMVar_hsa_circ_283641,RMVar_hsa_circ_304946,RMVar_hsa_circ_50765,RMVar_hsa_circ_250731,RMVar_hsa_circ_250733,RMVar_hsa_circ_250734,RMVar_hsa_circ_250732,RMVar_hsa_circ_315156,RMVar_hsa_circ_250730,RMVar_hsa_circ_265039,RMVar_hsa_circ_29905,RMVar_hsa_circ_50204 41150 RMVar_ID_41150 Human_SNP_ID_355761819 A-to-I Human chr8 + 22514036 22514036 22514036 GGGGTGCCTAGGCGGGCGGATCACTTAAGGCCAGGAGTTCGAGACCAGCCTGGCCAACATGGCAA GGGGTGCCTAGGCGGGCGGATCACTTAAGGCCCGGAGTTCGAGACCAGCCTGGCCAACATGGCAA A C PPP3CC Ensembl:ENSG00000120910 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1283741038 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_250721,RMVar_hsa_circ_20202,RMVar_hsa_circ_324113,RMVar_hsa_circ_311070,RMVar_hsa_circ_102699,RMVar_hsa_circ_56783,RMVar_hsa_circ_250723,RMVar_hsa_circ_250724,RMVar_hsa_circ_250722,RMVar_hsa_circ_39597,RMVar_hsa_circ_250720,RMVar_hsa_circ_359881,RMVar_hsa_circ_325507,RMVar_hsa_circ_304946,RMVar_hsa_circ_50765,RMVar_hsa_circ_250731,RMVar_hsa_circ_250733,RMVar_hsa_circ_250732,RMVar_hsa_circ_250730,RMVar_hsa_circ_265039,RMVar_hsa_circ_29905,RMVar_hsa_circ_50204,RMVar_hsa_circ_70780,RMVar_hsa_circ_36751,RMVar_hsa_circ_250737 41151 RMVar_ID_41151 Human_SNP_ID_355765681 A-to-I Human chr8 + 22529649 22529649 22529649 GGGATTATAGGCGCGTGCCACCATGACCAGCTAATTTTTGTATTTTTAGTATAGATGGGGTTTCG GGGATTATAGGCGCGTGCCACCATGACCAGCTTATTTTTGTATTTTTAGTATAGATGGGGTTTCG A T PPP3CC Ensembl:ENSG00000120910 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs994984878 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_250721,RMVar_hsa_circ_311070,RMVar_hsa_circ_102699,RMVar_hsa_circ_250722,RMVar_hsa_circ_250720,RMVar_hsa_circ_325507,RMVar_hsa_circ_250730,RMVar_hsa_circ_265039,RMVar_hsa_circ_29905,RMVar_hsa_circ_349051,RMVar_hsa_circ_351249,RMVar_hsa_circ_24512,RMVar_hsa_circ_332256 41152 RMVar_ID_41152 Human_SNP_ID_355765951 A-to-I Human chr8 + 22530784 22530784 22530784 AACCTGAGAGGCGGAGGTTGCAGTGAGCCAAGATCGCACTACTGCACTCCAGCCTGGCGACAGAG AACCTGAGAGGCGGAGGTTGCAGTGAGCCAAGTTCGCACTACTGCACTCCAGCCTGGCGACAGAG A T PPP3CC Ensembl:ENSG00000120910 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1355040676 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_250721,RMVar_hsa_circ_311070,RMVar_hsa_circ_102699,RMVar_hsa_circ_250722,RMVar_hsa_circ_250720,RMVar_hsa_circ_325507,RMVar_hsa_circ_250730,RMVar_hsa_circ_265039,RMVar_hsa_circ_29905,RMVar_hsa_circ_349051,RMVar_hsa_circ_351249,RMVar_hsa_circ_24512,RMVar_hsa_circ_332256 41153 RMVar_ID_41153 Human_SNP_ID_355767269 A-to-I Human chr8 + 22535932 22535932 22535932 TTTTTATATTTTAGTAGAGATGGGGTTTCACCATGTTGCCCAGGCTGGTCTGGAACTCCTGAGGT TTTTTATATTTTAGTAGAGATGGGGTTTCACCGTGTTGCCCAGGCTGGTCTGGAACTCCTGAGGT A G PPP3CC Ensembl:ENSG00000120910 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1352695768 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_250721,RMVar_hsa_circ_102699,RMVar_hsa_circ_250720 41154 RMVar_ID_41154 Human_SNP_ID_355767270 A-to-I Human chr8 + 22535941 22535941 22535941 TTTAGTAGAGATGGGGTTTCACCATGTTGCCCAGGCTGGTCTGGAACTCCTGAGGTCAGGCAATA TTTAGTAGAGATGGGGTTTCACCATGTTGCCCGGGCTGGTCTGGAACTCCTGAGGTCAGGCAATA A G PPP3CC Ensembl:ENSG00000120910 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs777791858 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_250721,RMVar_hsa_circ_102699,RMVar_hsa_circ_250720 41155 RMVar_ID_41155 Human_SNP_ID_355776691 A-to-I Human chr8 + 22570934 22570934 22570934 CCCCTCAGGGAGAGCACATCTGCCTGATCCGCAAGGTGAACGAGAACTGGTACGAGGGACGCATC CCCCTCAGGGAGAGCACATCTGCCTGATCCGCCAGGTGAACGAGAACTGGTACGAGGGACGCATC A C SORBS3 Ensembl:ENSG00000120896 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs556768810 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19021831 Human_Splice_Rec_957062,Human_Splice_Rec_957122,Human_Splice_Rec_957194,Human_Splice_Rec_957218,Human_Splice_Rec_957230,Human_Splice_Rec_957246,Human_Splice_Rec_957260 41156 RMVar_ID_41156 Human_SNP_ID_355777666 A-to-I Human chr8 + 22573997 22573997 22573997 AGGGGTGTGCAGGGAAAAGGGGCAGGGCTCTGAAGGTCGGCAACCCCGGCCTGGGTCCCCAGTGA AGGGGTGTGCAGGGAAAAGGGGCAGGGCTCTGCAGGTCGGCAACCCCGGCCTGGGTCCCCAGTGA A C SORBS3 Ensembl:ENSG00000120896 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs938637520 Functional Loss SNV dbSNP153 33..33 33 - - - 41157 RMVar_ID_41157 Human_SNP_ID_355783955 A-to-I Human chr8 + 22593483 22593483 22593483 CTTGTAATCCCAGCTACTCAGGAGGCTGGTGCAGGAGTATCGCTTGAACCCGGAAGGTAGAGATT CTTGTAATCCCAGCTACTCAGGAGGCTGGTGCCGGAGTATCGCTTGAACCCGGAAGGTAGAGATT A C PDLIM2,AC037459.1 Ensembl:ENSG00000120913,Ensembl:ENSG00000248235 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1258321334 Functional Loss SNV dbSNP153 33..33 33 - - - 41158 RMVar_ID_41158 Human_SNP_ID_355792596 A-to-I Human chr8 + 22616549 22616549 22616549 TTAACTAGAAAATTTTGTAGGCCGGGCGCTGTAGCTCACCCCTGTAATCCCAGCACTTTGGGAGA TTAACTAGAAAATTTTGTAGGCCGGGCGCTGTGGCTCACCCCTGTAATCCCAGCACTTTGGGAGA A G CCAR2 Ensembl:ENSG00000158941 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1474118194 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1040,RMVar_hsa_circ_13949,RMVar_hsa_circ_11191,RMVar_hsa_circ_85739,RMVar_hsa_circ_250757 41159 RMVar_ID_41159 Human_SNP_ID_355792653 A-to-I Human chr8 - 22616692 22616690 22616692 CCTGCCTCAGCCTCCCGAGTAGCTGAGAAAACAGGCATGCACCACCACACCCGGCTAATTTTTGT CCTGCCTCAGCCTCCCGAGTAGCTGAGAAAAC__GCATGCACCACCACACCCGGCTAATTTTTGT CCT C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1018328144 Functional Loss DEL dbSNP153 33..34 33 - - - 41160 RMVar_ID_41160 Human_SNP_ID_355792886 A-to-I Human chr8 + 22617075 22617075 22617075 CCAGCTAATTTTTGTAGAGATGGGGTTTCACCATGTTGGCCTGGCTGGTCTTGAACTCCTGACCT CCAGCTAATTTTTGTAGAGATGGGGTTTCACCGTGTTGGCCTGGCTGGTCTTGAACTCCTGACCT A G CCAR2 Ensembl:ENSG00000158941 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1330306918 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1040,RMVar_hsa_circ_13949,RMVar_hsa_circ_11191,RMVar_hsa_circ_85739,RMVar_hsa_circ_250757 41161 RMVar_ID_41161 Human_SNP_ID_355798482 A-to-I Human chr8 - 22631380 22631380 22631380 GCTGGCAGCTTTGGAGCTCTTTGTCCCGTACAAGTCCCCAGGTTTCCATTATTTACAAACAAAAT GCTGGCAGCTTTGGAGCTCTTTGTCCCGTACATGTCCCCAGGTTTCCATTATTTACAAACAAAAT T A BIN3 Ensembl:ENSG00000147439 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910537180 Functional Loss SNV dbSNP153 33..33 33 - - - 41162 RMVar_ID_41162 Human_SNP_ID_355799019 A-to-I Human chr8 - 22633211 22633211 22633211 CCTGCTTCAGCTTCCCAAAGCACAGGGATTACAGGCATGAGCCACTACGCCCAGCCAAGACCATG CCTGCTTCAGCTTCCCAAAGCACAGGGATTACCGGCATGAGCCACTACGCCCAGCCAAGACCATG T G BIN3 Ensembl:ENSG00000147439 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1274103499 Functional Loss SNV dbSNP153 33..33 33 - - - 41163 RMVar_ID_41163 Human_SNP_ID_355903515 A-to-I Human chr8 - 23024339 23024335 23024339 ATGTTCTGGAAGTGACGTGCTGCAGGTCTCAGAGCTGGCTGGTGGTCGGGGTCAGTACTGGACTG ATGTTCTGGAAGTGACGTGCTGCAGGTCTCAG____GGCTGGTGGTCGGGGTCAGTACTGGACTG CAGCT C TNFRSF10B Ensembl:ENSG00000120889 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1048250145 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_22688783 RMVar_hsa_circ_85268,RMVar_hsa_circ_250771 41164 RMVar_ID_41164 Human_SNP_ID_355903517 A-to-I Human chr8 - 23024339 23024339 23024339 ATGTTCTGGAAGTGACGTGCTGCAGGTCTCAGAGCTGGCTGGTGGTCGGGGTCAGTACTGGACTG ATGTTCTGGAAGTGACGTGCTGCAGGTCTCAGTGCTGGCTGGTGGTCGGGGTCAGTACTGGACTG T A TNFRSF10B Ensembl:ENSG00000120889 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6557609 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22688783 GWAS_ID_4779 RMVar_hsa_circ_85268,RMVar_hsa_circ_250771 41165 RMVar_ID_41165 Human_SNP_ID_355903518 A-to-I Human chr8 - 23024339 23024339 23024339 ATGTTCTGGAAGTGACGTGCTGCAGGTCTCAGAGCTGGCTGGTGGTCGGGGTCAGTACTGGACTG ATGTTCTGGAAGTGACGTGCTGCAGGTCTCAGGGCTGGCTGGTGGTCGGGGTCAGTACTGGACTG T C TNFRSF10B Ensembl:ENSG00000120889 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6557609 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22688783 GWAS_ID_4779 RMVar_hsa_circ_85268,RMVar_hsa_circ_250771 41166 RMVar_ID_41166 Human_SNP_ID_355915453 A-to-I Human chr8 - 23067116 23067116 23067116 AAATTAGCTGGGTGTGGTGGTGGGCACCTGCAATCCCAGCTACTTGGGAGGTTGAGGCAGGAGAA AAATTAGCTGGGTGTGGTGGTGGGCACCTGCAGTCCCAGCTACTTGGGAGGTTGAGGCAGGAGAA T C TNFRSF10B Ensembl:ENSG00000120889 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1346386826 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_250773,RMVar_hsa_circ_112959 41167 RMVar_ID_41167 Human_SNP_ID_355922900 A-to-I Human chr8 + 23095030 23095030 23095030 ACGATCTCGGCTCACTGCAAGCTCCGCCCCCTAGGTTCCTACCATTCTCCTGCCTCAGCCTCCCG ACGATCTCGGCTCACTGCAAGCTCCGCCCCCTGGGTTCCTACCATTCTCCTGCCTCAGCCTCCCG A G AC107959.4,AC107959.5 Ensembl:ENSG00000284948,Ensembl:ENSG00000284956 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs943247143 Functional Loss SNV dbSNP153 33..33 33 - - - 41168 RMVar_ID_41168 Human_SNP_ID_355942049 A-to-I Human chr8 - 23159629 23159629 23159629 TCGAAGTCGAGCTCAGGTGATCCGCCCATCTCAGCCTTCCAAAATGCTGGGATTACAGGTGTGTG TCGAAGTCGAGCTCAGGTGATCCGCCCATCTCGGCCTTCCAAAATGCTGGGATTACAGGTGTGTG T C TNFRSF10D Ensembl:ENSG00000173530 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277336732 Functional Loss SNV dbSNP153 33..33 33 - - - 41169 RMVar_ID_41169 Human_SNP_ID_355942050 A-to-I Human chr8 - 23159629 23159629 23159629 TCGAAGTCGAGCTCAGGTGATCCGCCCATCTCAGCCTTCCAAAATGCTGGGATTACAGGTGTGTG TCGAAGTCGAGCTCAGGTGATCCGCCCATCTCCGCCTTCCAAAATGCTGGGATTACAGGTGTGTG T G TNFRSF10D Ensembl:ENSG00000173530 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277336732 Functional Loss SNV dbSNP153 33..33 33 - - - 41170 RMVar_ID_41170 Human_SNP_ID_355951049 A-to-I Human chr8 - 23188324 23188324 23188324 TTAATCATTCATGAGAAGCCTCCCACGACCCAATCACCTCCCACCAGGCCTTACCTCCAACATCT TTAATCATTCATGAGAAGCCTCCCACGACCCAGTCACCTCCCACCAGGCCTTACCTCCAACATCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1036624108 Functional Loss SNV dbSNP153 33..33 33 - - - 41171 RMVar_ID_41171 Human_SNP_ID_355951066 A-to-I Human chr8 - 23188388 23188385 23188389 TACAAACAACCAGATCTCAGGACAACTCACTCAGTATCAGGAGAACAGCACCACAAAATTGTGGT TACAAACAACCAGATCTCAGGACAACTCACT____ATCAGGAGAACAGCACCACAAAATTGTGGT TACTG T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1363453485 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_8684911 41172 RMVar_ID_41172 Human_SNP_ID_355951071 A-to-I Human chr8 - 23188396 23188396 23188396 CACACACTTACAAACAACCAGATCTCAGGACAACTCACTCAGTATCAGGAGAACAGCACCACAAA CACACACTTACAAACAACCAGATCTCAGGACAGCTCACTCAGTATCAGGAGAACAGCACCACAAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251118837 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8684911 41173 RMVar_ID_41173 Human_SNP_ID_355951073 A-to-I Human chr8 - 23188402 23188402 23188402 AGGTGCCACACACTTACAAACAACCAGATCTCAGGACAACTCACTCAGTATCAGGAGAACAGCAC AGGTGCCACACACTTACAAACAACCAGATCTCCGGACAACTCACTCAGTATCAGGAGAACAGCAC T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs889781467 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8684911 41174 RMVar_ID_41174 Human_SNP_ID_355951101 A-to-I Human chr8 - 23188500 23188500 23188500 TTCTGCTTCTAGGAGACCTCAGGAAGCCTCCAATCATGGCAGAAGGCAAAGGGGGAGTGAGCTGT TTCTGCTTCTAGGAGACCTCAGGAAGCCTCCAGTCATGGCAGAAGGCAAAGGGGGAGTGAGCTGT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474144781 Functional Loss SNV dbSNP153 33..33 33 - - - 41175 RMVar_ID_41175 Human_SNP_ID_355951103 A-to-I Human chr8 - 23188508 23188508 23188508 ATGGCAGCTTCTGCTTCTAGGAGACCTCAGGAAGCCTCCAATCATGGCAGAAGGCAAAGGGGGAG ATGGCAGCTTCTGCTTCTAGGAGACCTCAGGATGCCTCCAATCATGGCAGAAGGCAAAGGGGGAG T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1188328177 Functional Loss SNV dbSNP153 33..33 33 - - - 41176 RMVar_ID_41176 Human_SNP_ID_355951129 A-to-I Human chr8 - 23188596 23188596 23188596 GCATTGCTATAAAGAAATACCTAAGCCTGAGTAATTTATAAAGAAAAGAAGTTAATTAGCTCACG GCATTGCTATAAAGAAATACCTAAGCCTGAGTCATTTATAAAGAAAAGAAGTTAATTAGCTCACG T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1392127042 Functional Loss SNV dbSNP153 33..33 33 - - - 41177 RMVar_ID_41177 Human_SNP_ID_355951210 A-to-I Human chr8 - 23188960 23188960 23188960 TCATGAGATCTGATTGTTAAAAAATGTGTGGCACCTCCCCATTCTCTCTTCCTCCTGCTCTGGCC TCATGAGATCTGATTGTTAAAAAATGTGTGGCCCCTCCCCATTCTCTCTTCCTCCTGCTCTGGCC T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334003684 Functional Loss SNV dbSNP153 33..33 33 - - - 41178 RMVar_ID_41178 Human_SNP_ID_355951217 A-to-I Human chr8 - 23188997 23188994 23188998 TCCTCTCGGTACTGTCCTTCTGACAGTGAGTGAGTTCTCATGAGATCTGATTGTTAAAAAATGTG TCCTCTCGGTACTGTCCTTCTGACAGTGAGT____TCTCATGAGATCTGATTGTTAAAAAATGTG AACTC A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1428292833 Functional Loss DEL dbSNP153 32..35 33 - - - 41179 RMVar_ID_41179 Human_SNP_ID_355951221 A-to-I Human chr8 - 23189019 23189019 23189019 CTCATAAATGTTTTAACACCATTCCTCTCGGTACTGTCCTTCTGACAGTGAGTGAGTTCTCATGA CTCATAAATGTTTTAACACCATTCCTCTCGGTGCTGTCCTTCTGACAGTGAGTGAGTTCTCATGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1050273867 Functional Loss SNV dbSNP153 33..33 33 - - - 41180 RMVar_ID_41180 Human_SNP_ID_355951232 A-to-I Human chr8 - 23189046 23189046 23189046 AGGTGATTGGATTATGAGGGCAGATTTCTCATAAATGTTTTAACACCATTCCTCTCGGTACTGTC AGGTGATTGGATTATGAGGGCAGATTTCTCATGAATGTTTTAACACCATTCCTCTCGGTACTGTC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1011282782 Functional Loss SNV dbSNP153 33..33 33 - - - 41181 RMVar_ID_41181 Human_SNP_ID_355951244 A-to-I Human chr8 - 23189109 23189109 23189109 TGTGGCCCCACCAAAGTCTCATGTTGAATTGTAGTCCCCAGTGTTGGAGGTGGGGCCTGGTGGAG TGTGGCCCCACCAAAGTCTCATGTTGAATTGTTGTCCCCAGTGTTGGAGGTGGGGCCTGGTGGAG T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1035995539 Functional Loss SNV dbSNP153 33..33 33 - - - 41182 RMVar_ID_41182 Human_SNP_ID_355951855 A-to-I Human chr8 - 23191472 23191472 23191472 AACATCGTGAAATGCCGTCTTTACAAAAAAATACAAAAATTAACTGGATGTGATGGTGTGTGCAT AACATCGTGAAATGCCGTCTTTACAAAAAAATTCAAAAATTAACTGGATGTGATGGTGTGTGCAT T A TNFRSF10A Ensembl:ENSG00000104689 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1262799694 Functional Loss SNV dbSNP153 33..33 33 - - - 41183 RMVar_ID_41183 Human_SNP_ID_355972490 A-to-I Human chr8 - 23263690 23263690 23263690 GGAAGGTCACCAGGCTCACCCACAAGCCTCAGAGCAGGGCTTCGTTTTGATTCTTTGGGACTCAG GGAAGGTCACCAGGCTCACCCACAAGCCTCAGGGCAGGGCTTCGTTTTGATTCTTTGGGACTCAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs958895408 Functional Loss SNV dbSNP153 33..33 33 - - - 41184 RMVar_ID_41184 Human_SNP_ID_355990132 A-to-I Human chr8 - 23322228 23322228 23322228 ACGAGATCCAGTGCACAGGCAATGAGAAGTCCATTATAGACTGCAAGTTCAATGCCGAGTCTCAG ACGAGATCCAGTGCACAGGCAATGAGAAGTCCGTTATAGACTGCAAGTTCAATGCCGAGTCTCAG T C LOXL2 Ensembl:ENSG00000134013 Protein coding CDS GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs774478852 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 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 41185 RMVar_ID_41185 Human_SNP_ID_356492871 A-to-I Human chr8 + 25260875 25260875 25260875 TGGAGTGCAGTGGCGCGATCATAGCTGACTGCAGCCTCCAACTTCTGGGCTCAAGAGATCCTCTG TGGAGTGCAGTGGCGCGATCATAGCTGACTGCTGCCTCCAACTTCTGGGCTCAAGAGATCCTCTG A T DOCK5 Ensembl:ENSG00000147459 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1019663006 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_250819,RMVar_hsa_circ_250820,RMVar_hsa_circ_350142,RMVar_hsa_circ_359708,RMVar_hsa_circ_278022 41186 RMVar_ID_41186 Human_SNP_ID_356502012 A-to-I Human chr8 + 25298006 25298006 25298006 TTGAGACTGGGAATTTAAGGCTGTAGTGAACTATGATCATACCACTGCACTCCAGCCTGGGCAAC TTGAGACTGGGAATTTAAGGCTGTAGTGAACTCTGATCATACCACTGCACTCCAGCCTGGGCAAC A C DOCK5 Ensembl:ENSG00000147459 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893264937 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26163047 RMVar_hsa_circ_16403,RMVar_hsa_circ_96450,RMVar_hsa_circ_250822,RMVar_hsa_circ_347036,RMVar_hsa_circ_359968,RMVar_hsa_circ_312645,RMVar_hsa_circ_333430,RMVar_hsa_circ_298014,RMVar_hsa_circ_32485,RMVar_hsa_circ_35702,RMVar_hsa_circ_4554,RMVar_hsa_circ_10358,RMVar_hsa_circ_32884,RMVar_hsa_circ_51196,RMVar_hsa_circ_314780,RMVar_hsa_circ_342182,RMVar_hsa_circ_53719,RMVar_hsa_circ_347373,RMVar_hsa_circ_250824,RMVar_hsa_circ_29892,RMVar_hsa_circ_250823,RMVar_hsa_circ_56079,RMVar_hsa_circ_342902,RMVar_hsa_circ_54760,RMVar_hsa_circ_78420,RMVar_hsa_circ_250826,RMVar_hsa_circ_267891,RMVar_hsa_circ_332130,RMVar_hsa_circ_100339,RMVar_hsa_circ_44616,RMVar_hsa_circ_250827,RMVar_hsa_circ_250828 41187 RMVar_ID_41187 Human_SNP_ID_356516765 A-to-I Human chr8 + 25355481 25355477 25355481 TGTTTATTTATTTTGTTTTGAGACAGGGTGTCACTCTGTCAGCCAGGCTGGAGTGCAGGGGTGCT TGTTTATTTATTTTGTTTTGAGACAGGGT____CTCTGTCAGCCAGGCTGGAGTGCAGGGGTGCT TGTCA T DOCK5 Ensembl:ENSG00000147459 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs775383330 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_3348,RMVar_hsa_circ_32485,RMVar_hsa_circ_35702,RMVar_hsa_circ_53719,RMVar_hsa_circ_29892,RMVar_hsa_circ_78420,RMVar_hsa_circ_250827,RMVar_hsa_circ_367180,RMVar_hsa_circ_112983,RMVar_hsa_circ_86116,RMVar_hsa_circ_62701,RMVar_hsa_circ_250836,RMVar_hsa_circ_4994,RMVar_hsa_circ_250837,RMVar_hsa_circ_8470,RMVar_hsa_circ_250838,RMVar_hsa_circ_75538,RMVar_hsa_circ_66239,RMVar_hsa_circ_64252,RMVar_hsa_circ_97886,RMVar_hsa_circ_39590,RMVar_hsa_circ_250848,RMVar_hsa_circ_76866,RMVar_hsa_circ_24483,RMVar_hsa_circ_78707,RMVar_hsa_circ_250851,RMVar_hsa_circ_250852,RMVar_hsa_circ_21290,RMVar_hsa_circ_326846,RMVar_hsa_circ_67366,RMVar_hsa_circ_324970,RMVar_hsa_circ_10305,RMVar_hsa_circ_56345 41188 RMVar_ID_41188 Human_SNP_ID_356516813 A-to-I Human chr8 + 25355650 25355650 25355650 TTTTGTATTTTTAGCAGAGACGAGGTTTTGCCATGTTGGCCGGGCTAGTCTTGATCTCCTGACCT TTTTGTATTTTTAGCAGAGACGAGGTTTTGCCCTGTTGGCCGGGCTAGTCTTGATCTCCTGACCT A C DOCK5 Ensembl:ENSG00000147459 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1464584232 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3348,RMVar_hsa_circ_32485,RMVar_hsa_circ_35702,RMVar_hsa_circ_53719,RMVar_hsa_circ_29892,RMVar_hsa_circ_78420,RMVar_hsa_circ_250827,RMVar_hsa_circ_367180,RMVar_hsa_circ_112983,RMVar_hsa_circ_86116,RMVar_hsa_circ_62701,RMVar_hsa_circ_250836,RMVar_hsa_circ_4994,RMVar_hsa_circ_250837,RMVar_hsa_circ_8470,RMVar_hsa_circ_250838,RMVar_hsa_circ_75538,RMVar_hsa_circ_66239,RMVar_hsa_circ_64252,RMVar_hsa_circ_97886,RMVar_hsa_circ_39590,RMVar_hsa_circ_250848,RMVar_hsa_circ_76866,RMVar_hsa_circ_24483,RMVar_hsa_circ_78707,RMVar_hsa_circ_250851,RMVar_hsa_circ_250852,RMVar_hsa_circ_21290,RMVar_hsa_circ_326846,RMVar_hsa_circ_67366,RMVar_hsa_circ_324970,RMVar_hsa_circ_10305,RMVar_hsa_circ_56345 41189 RMVar_ID_41189 Human_SNP_ID_356524801 A-to-I Human chr8 + 25384694 25384694 25384694 GTTGGCCAGGCTGATCTCGAACTCCTGACCTCAGTTGATCCCCCTGCCTCAGCCTCCCAAAGTTT GTTGGCCAGGCTGATCTCGAACTCCTGACCTCTGTTGATCCCCCTGCCTCAGCCTCCCAAAGTTT A T DOCK5 Ensembl:ENSG00000147459 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1220511370 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 41190 RMVar_ID_41190 Human_SNP_ID_356525243 A-to-I Human chr8 + 25386475 25386475 25386475 TTAAAAATTAGCCAGGCATGGTAGCATGTGCTATGGTCCTAGCTACTCAGTAGGCTGAGGCAGGA TTAAAAATTAGCCAGGCATGGTAGCATGTGCTGTGGTCCTAGCTACTCAGTAGGCTGAGGCAGGA A G DOCK5 Ensembl:ENSG00000147459 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs894295154 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 41191 RMVar_ID_41191 Human_SNP_ID_356525479 A-to-I Human chr8 + 25387318 25387318 25387318 ATCCTGCCTCAGCCTCCTGAGGAGGTGGGATTACAGGTGTGCACCATCACGCCCAGTTAATGTTT ATCCTGCCTCAGCCTCCTGAGGAGGTGGGATTGCAGGTGTGCACCATCACGCCCAGTTAATGTTT A G DOCK5 Ensembl:ENSG00000147459 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1273815198 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 41192 RMVar_ID_41192 Human_SNP_ID_356671496 A-to-I Human chr8 - 25943427 25943427 25943427 TAACTTACTGTAGCCTCAAACTCCTGGGTTCAAGAGATTCTCCTGTCTCAGCCTCCCAAGTAGCT TAACTTACTGTAGCCTCAAACTCCTGGGTTCACGAGATTCTCCTGTCTCAGCCTCCCAAGTAGCT T G EBF2 Ensembl:ENSG00000221818 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs901905842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17434487 41193 RMVar_ID_41193 Human_SNP_ID_356764911 A-to-I Human chr8 + 26299140 26299140 26299140 TACAAAAATTAAAAATATTAGCAGGGCATGGCAGTGTGCAACTGTAGTCCCAGCTACTAAGGAGG TACAAAAATTAAAAATATTAGCAGGGCATGGCCGTGTGCAACTGTAGTCCCAGCTACTAAGGAGG A C PPP2R2A Ensembl:ENSG00000221914 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1287283508 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_697727,Human_RBP_ID_7826212 RMVar_hsa_circ_59757 41194 RMVar_ID_41194 Human_SNP_ID_356782882 A-to-I Human chr8 + 26369599 26369599 26369599 TATTTTTAGTAGAGACCGGGTTTCACCATGTTAGCCAGAATGGTCTCGATCTCCTGACGTCGTGA TATTTTTAGTAGAGACCGGGTTTCACCATGTTGGCCAGAATGGTCTCGATCTCCTGACGTCGTGA A G PPP2R2A Ensembl:ENSG00000221914 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs143055052 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3154106 RMVar_hsa_circ_250885,RMVar_hsa_circ_250891 41195 RMVar_ID_41195 Human_SNP_ID_356782884 A-to-I Human chr8 + 26369605 26369605 26369605 TAGTAGAGACCGGGTTTCACCATGTTAGCCAGAATGGTCTCGATCTCCTGACGTCGTGATCTGCC TAGTAGAGACCGGGTTTCACCATGTTAGCCAGGATGGTCTCGATCTCCTGACGTCGTGATCTGCC A G PPP2R2A Ensembl:ENSG00000221914 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs565996037 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3154106 RMVar_hsa_circ_250885,RMVar_hsa_circ_250891 41196 RMVar_ID_41196 Human_SNP_ID_356787092 A-to-I Human chr8 + 26384990 26384990 26384990 GAGGGGGTTGTTGGTCTCTCACCATGTTGGCCAGGCTGGTCTCAAACTCCTGACCTCACGTCATC GAGGGGGTTGTTGGTCTCTCACCATGTTGGCCGGGCTGGTCTCAAACTCCTGACCTCACGTCATC A G BNIP3L Ensembl:ENSG00000104765 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982882436 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_250896,RMVar_hsa_circ_96049 41197 RMVar_ID_41197 Human_SNP_ID_356792116 A-to-I Human chr8 + 26404717 26404717 26404717 TTTAGTAGAGACAGGGTTTCGCCGTGCTGGCCAGGCTGGTCTCAAACTCCTAACCTCAAGTGATC TTTAGTAGAGACAGGGTTTCGCCGTGCTGGCCGGGCTGGTCTCAAACTCCTAACCTCAAGTGATC A G BNIP3L Ensembl:ENSG00000104765 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924065226 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_250896,RMVar_hsa_circ_96049,RMVar_hsa_circ_250898,RMVar_hsa_circ_277736,RMVar_hsa_circ_250899 41198 RMVar_ID_41198 Human_SNP_ID_356806737 A-to-I Human chr8 + 26462841 26462841 26462841 GCGATCCTCCCTCCTCAGAATCCCAAGTAGCTAGGACCACAGGCACACGCCACCTTGCCTGGCTA GCGATCCTCCCTCCTCAGAATCCCAAGTAGCTGGGACCACAGGCACACGCCACCTTGCCTGGCTA A G BNIP3L Ensembl:ENSG00000104765 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1160166538 Functional Loss SNV dbSNP153 33..33 33 - - - 41199 RMVar_ID_41199 Human_SNP_ID_356842608 A-to-I Human chr8 + 26601711 26601711 26601711 TCTCTTATAGGAACTTCAGGTGCTAATGTTGCAGGATTTAGGAGGACGAGAGAGACCTTGGGTTG TCTCTTATAGGAACTTCAGGTGCTAATGTTGCCGGATTTAGGAGGACGAGAGAGACCTTGGGTTG A C DPYSL2 Ensembl:ENSG00000092964 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1481533687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16399075,Human_RBP_ID_23316071 RMVar_hsa_circ_103604,RMVar_hsa_circ_250902,RMVar_hsa_circ_98520,RMVar_hsa_circ_42545,RMVar_hsa_circ_115395,RMVar_hsa_circ_250906,RMVar_hsa_circ_315449,RMVar_hsa_circ_250907,RMVar_hsa_circ_300634,RMVar_hsa_circ_48490,RMVar_hsa_circ_250909 41200 RMVar_ID_41200 Human_SNP_ID_356853511 A-to-I Human chr8 + 26645198 26645198 26645198 GAGGTGGGTGAATTATTTGAGCCCAGGAGTTCAAGACCAGTCTGGCAACATGGCAAAACCCTGTC GAGGTGGGTGAATTATTTGAGCCCAGGAGTTCGAGACCAGTCTGGCAACATGGCAAAACCCTGTC A G DPYSL2 Ensembl:ENSG00000092964 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs984404306 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4710,RMVar_hsa_circ_103604,RMVar_hsa_circ_250902,RMVar_hsa_circ_42545,RMVar_hsa_circ_115395,RMVar_hsa_circ_250907,RMVar_hsa_circ_105976,RMVar_hsa_circ_90084,RMVar_hsa_circ_25806,RMVar_hsa_circ_250911,RMVar_hsa_circ_327126,RMVar_hsa_circ_250913,RMVar_hsa_circ_250917,RMVar_hsa_circ_250916 41201 RMVar_ID_41201 Human_SNP_ID_356855807 A-to-I Human chr8 + 26655268 26655268 26655268 CCTCTTATCCCAGCACTTTGGGAGGCAGAGGTAGGAGGATTGCTTGAGCCCAGGAGTTTGAGACC CCTCTTATCCCAGCACTTTGGGAGGCAGAGGTGGGAGGATTGCTTGAGCCCAGGAGTTTGAGACC A G DPYSL2 Ensembl:ENSG00000092964 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs577541941 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126649,RMVar_hsa_circ_115395,RMVar_hsa_circ_250907,RMVar_hsa_circ_105976,RMVar_hsa_circ_90084,RMVar_hsa_circ_250911,RMVar_hsa_circ_250916,RMVar_hsa_circ_250919,RMVar_hsa_circ_124487,RMVar_hsa_circ_250920 41202 RMVar_ID_41202 Human_SNP_ID_357016065 A-to-I Human chr8 - 27282189 27282189 27282189 TCACTGCAACCCCCGCCTCCCAGGTTCGAGCAATTCTCCTGTCTCAGCCTCCTGAGTAGCTGGGA TCACTGCAACCCCCGCCTCCCAGGTTCGAGCAGTTCTCCTGTCTCAGCCTCCTGAGTAGCTGGGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1249853038 Functional Loss SNV dbSNP153 33..33 33 - - - 41203 RMVar_ID_41203 Human_SNP_ID_357018275 A-to-I Human chr8 - 27290454 27290454 27290454 ACCCAGTCTCATGACAACTAAACCACTTCACAATAACGGTATTAATCCATTTGTGAGGGCTCTGC ACCCAGTCTCATGACAACTAAACCACTTCACAGTAACGGTATTAATCCATTTGTGAGGGCTCTGC T C TRIM35 Ensembl:ENSG00000104228 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs978905642 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81587,RMVar_hsa_circ_250932 41204 RMVar_ID_41204 Human_SNP_ID_357018668 A-to-I Human chr8 - 27292017 27292017 27292017 GGTTTAAATATGTTCCCCAAAATTTATGTGTTACAAACTTAATCCCCAATGCAACAGTGTTGGGT GGTTTAAATATGTTCCCCAAAATTTATGTGTTGCAAACTTAATCCCCAATGCAACAGTGTTGGGT T C TRIM35 Ensembl:ENSG00000104228 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1281246331 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81587,RMVar_hsa_circ_250932 41205 RMVar_ID_41205 Human_SNP_ID_357095737 A-to-I Human chr8 + 27593514 27593514 27593514 CTGGCTCACTGCAACCTCCGCCTCCCGGATTCAAGCAGTTCTCCTGCCTCAGCCTCCCAAGCAGC CTGGCTCACTGCAACCTCCGCCTCCCGGATTCTAGCAGTTCTCCTGCCTCAGCCTCCCAAGCAGC A T lnc-SCARA3-2,lnc-SCARA3-2:2,lnc-SCARA3-2:3,lnc-SCARA3-2:4,lnc-SCARA3-2:5 RNACentral:URS00008B9593,RNACentral:URS00009B0F16,RNACentral:URS00009AFA74,RNACentral:URS00009C2A7E,RNACentral:URS00008B4B30 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs183448094 Functional Loss SNV dbSNP153 33..33 33 - - - 41206 RMVar_ID_41206 Human_SNP_ID_357097777 A-to-I Human chr8 - 27600323 27600323 27600323 GGCTGAGGTTGGAGGACAGCCTGAGCCTGGGAAGTCAAGGCTGCAGTGAGCCGAGATCTCACCAC GGCTGAGGTTGGAGGACAGCCTGAGCCTGGGAGGTCAAGGCTGCAGTGAGCCGAGATCTCACCAC T C CLU Ensembl:ENSG00000120885 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1343794124 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61531,RMVar_hsa_circ_82519,RMVar_hsa_circ_250949,RMVar_hsa_circ_336627,RMVar_hsa_circ_250950 41207 RMVar_ID_41207 Human_SNP_ID_357097788 A-to-I Human chr8 - 27600375 27600375 27600375 CAAAAATTAGCTGGGCATGGTAGCATGTGCCTATAGTCCCAGCTACTCAGGAGGCTGAGGTTGGA CAAAAATTAGCTGGGCATGGTAGCATGTGCCTCTAGTCCCAGCTACTCAGGAGGCTGAGGTTGGA T G CLU Ensembl:ENSG00000120885 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs981541245 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61531,RMVar_hsa_circ_82519,RMVar_hsa_circ_250949,RMVar_hsa_circ_336627,RMVar_hsa_circ_250950 41208 RMVar_ID_41208 Human_SNP_ID_357138428 A-to-I Human chr8 - 27764366 27764366 27764366 TACTCTGGAGGCTGAGGCAGGAAGATCGCTTGAGCCTGGGAGGTAGGCTGCAGTGAGCTGTGATC TACTCTGGAGGCTGAGGCAGGAAGATCGCTTGCGCCTGGGAGGTAGGCTGCAGTGAGCTGTGATC T G CCDC25 Ensembl:ENSG00000147419 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs538385620 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_961485 RMVar_hsa_circ_335705,RMVar_hsa_circ_364375 41209 RMVar_ID_41209 Human_SNP_ID_357165296 A-to-I Human chr8 - 27870224 27870214 27870225 TGCAAGGTTTGCATTTAAGTTAAAAAAAAAAAAAAAAAAAAACTAAAGGTGAAAGATGCCACATT TGCAAGGTTTGCATTTAAGTTAAAAAAAAAA___________CTAAAGGTGAAAGATGCCACATT GTTTTTTTTTTT G SCARA5 Ensembl:ENSG00000168079 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs11321344 Functional Loss DEL dbSNP153 32..42 33 - - - 41210 RMVar_ID_41210 Human_SNP_ID_357165297 A-to-I Human chr8 - 27870224 27870214 27870225 TGCAAGGTTTGCATTTAAGTTAAAAAAAAAAAAAAAAAAAAACTAAAGGTGAAAGATGCCACATT TGCAAGGTTTGCATTTAAGTTAAAAAAAAAA_____AAAAAACTAAAGGTGAAAGATGCCACATT GTTTTTTTTTTT GTTTTTT SCARA5 Ensembl:ENSG00000168079 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs11321344 Functional Loss DEL dbSNP153 32..36 33 - - - 41211 RMVar_ID_41211 Human_SNP_ID_357165298 A-to-I Human chr8 - 27870224 27870214 27870225 TGCAAGGTTTGCATTTAAGTTAAAAAAAAAAAAAAAAAAAAACTAAAGGTGAAAGATGCCACATT TGCAAGGTTTGCATTTAAGTTAAAAAAAAAA____AAAAAAACTAAAGGTGAAAGATGCCACATT GTTTTTTTTTTT GTTTTTTT SCARA5 Ensembl:ENSG00000168079 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs11321344 Functional Loss DEL dbSNP153 32..35 33 - - - 41212 RMVar_ID_41212 Human_SNP_ID_357165299 A-to-I Human chr8 - 27870224 27870214 27870225 TGCAAGGTTTGCATTTAAGTTAAAAAAAAAAAAAAAAAAAAACTAAAGGTGAAAGATGCCACATT TGCAAGGTTTGCATTTAAGTTAAAAAAAAAA___AAAAAAAACTAAAGGTGAAAGATGCCACATT GTTTTTTTTTTT GTTTTTTTT SCARA5 Ensembl:ENSG00000168079 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs11321344 Functional Loss DEL dbSNP153 32..34 33 - - - 41213 RMVar_ID_41213 Human_SNP_ID_357165300 A-to-I Human chr8 - 27870224 27870214 27870225 TGCAAGGTTTGCATTTAAGTTAAAAAAAAAAAAAAAAAAAAACTAAAGGTGAAAGATGCCACATT TGCAAGGTTTGCATTTAAGTTAAAAAAAAAA__AAAAAAAAACTAAAGGTGAAAGATGCCACATT GTTTTTTTTTTT GTTTTTTTTT SCARA5 Ensembl:ENSG00000168079 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs11321344 Functional Loss DEL dbSNP153 32..33 33 - - - 41214 RMVar_ID_41214 Human_SNP_ID_357165309 A-to-I Human chr8 - 27870224 27870224 27870224 TGCAAGGTTTGCATTTAAGTTAAAAAAAAAAAAAAAAAAAAACTAAAGGTGAAAGATGCCACATT TGCAAGGTTTGCATTTAAGTTAAAAAAAAAAACAAAAAAAAACTAAAGGTGAAAGATGCCACATT T G SCARA5 Ensembl:ENSG00000168079 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs956594752 Functional Loss SNV dbSNP153 33..33 33 - - - 41215 RMVar_ID_41215 Human_SNP_ID_357204199 A-to-I Human chr8 - 28022287 28022287 28022287 AGGCGTGGTAGCATGTGCCTATAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAA AGGCGTGGTAGCATGTGCCTATAGTCCCAGCTGCTTGGGAGGCTGAGGCAGGAGAATCGCTTGAA T C NUGGC Ensembl:ENSG00000189233 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1043215693 Functional Loss SNV dbSNP153 33..33 33 - - - 41216 RMVar_ID_41216 Human_SNP_ID_357204202 A-to-I Human chr8 - 28022310 28022310 28022310 ACTAAAAATACAAAAAATTAGCCAGGCGTGGTAGCATGTGCCTATAGTCCCAGCTACTTGGGAGG ACTAAAAATACAAAAAATTAGCCAGGCGTGGTGGCATGTGCCTATAGTCCCAGCTACTTGGGAGG T C NUGGC Ensembl:ENSG00000189233 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1466563316 Functional Loss SNV dbSNP153 33..33 33 - - - 41217 RMVar_ID_41217 Human_SNP_ID_357237950 A-to-I Human chr8 + 28160718 28160718 28160718 TTGAACCACATGGAATTGGTTTTTTTTGAGACAGAGCCTCACTTTGTCACCCAGGCCAGAGTGCA TTGAACCACATGGAATTGGTTTTTTTTGAGACGGAGCCTCACTTTGTCACCCAGGCCAGAGTGCA A G ELP3 Ensembl:ENSG00000134014 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170926350 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_324756,RMVar_hsa_circ_363603,RMVar_hsa_circ_76638,RMVar_hsa_circ_250975,RMVar_hsa_circ_271292,RMVar_hsa_circ_250978,RMVar_hsa_circ_250976,RMVar_hsa_circ_297746,RMVar_hsa_circ_271403,RMVar_hsa_circ_250980,RMVar_hsa_circ_339187 41218 RMVar_ID_41218 Human_SNP_ID_357271083 A-to-I Human chr8 + 28299843 28299843 28299843 ATACAGCACACCCAAATACAGGATGATAGTTCATGTAACAAACAGAGATATCATTTATCAGATTG ATACAGCACACCCAAATACAGGATGATAGTTCCTGTAACAAACAGAGATATCATTTATCAGATTG A C RPL5P22 Ensembl:ENSG00000239198 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1324357837 Functional Loss SNV dbSNP153 33..33 33 - - - 41219 RMVar_ID_41219 Human_SNP_ID_357282360 A-to-I Human chr8 - 28343149 28343149 28343149 AGAGATGGGGCTATTGAAATGGTAGCTAGAGGAATTACAAAAATACACTCTGATGTAGCAACAGG AGAGATGGGGCTATTGAAATGGTAGCTAGAGGTATTACAAAAATACACTCTGATGTAGCAACAGG T A - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs895391089 Functional Loss SNV dbSNP153 33..33 33 - - - 41220 RMVar_ID_41220 Human_SNP_ID_357286742 A-to-I Human chr8 - 28359264 28359264 28359264 CCGAGTAACTGGGATTACAGGCGTGCACCACCACGCCTGGCTAATTTTTGTATTTTTTGGTAGAG CCGAGTAACTGGGATTACAGGCGTGCACCACCGCGCCTGGCTAATTTTTGTATTTTTTGGTAGAG T C ZNF395,FBXO16 Ensembl:ENSG00000186918,Ensembl:ENSG00000214050 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1391015549 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_250981,RMVar_hsa_circ_370258,RMVar_hsa_circ_4566,RMVar_hsa_circ_87906,RMVar_hsa_circ_357512,RMVar_hsa_circ_250983 41221 RMVar_ID_41221 Human_SNP_ID_357286748 A-to-I Human chr8 - 28359280 28359279 28359280 CTTCCACTTCAGCCTCCCGAGTAACTGGGATTACAGGCGTGCACCACCACGCCTGGCTAATTTTT CTTCCACTTCAGCCTCCCGAGTAACTGGGATT_CAGGCGTGCACCACCACGCCTGGCTAATTTTT GT G ZNF395,FBXO16 Ensembl:ENSG00000186918,Ensembl:ENSG00000214050 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1163720098 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_250981,RMVar_hsa_circ_370258,RMVar_hsa_circ_4566,RMVar_hsa_circ_87906,RMVar_hsa_circ_357512,RMVar_hsa_circ_250983 41222 RMVar_ID_41222 Human_SNP_ID_357289135 A-to-I Human chr8 - 28368882 28368882 28368882 GCAGTGAGCCGAGATGGCGCCACTGCACCCCAACCTGGTCGACAGAGCGAGACTCTATCTCAAAA GCAGTGAGCCGAGATGGCGCCACTGCACCCCAGCCTGGTCGACAGAGCGAGACTCTATCTCAAAA T C ZNF395,FBXO16 Ensembl:ENSG00000186918,Ensembl:ENSG00000214050 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs972470248 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87906,RMVar_hsa_circ_250983 41223 RMVar_ID_41223 Human_SNP_ID_357289774 A-to-I Human chr8 - 28371460 28371460 28371460 AGAGCATAGCTTGTCTGGGTCTGGTGGCTCACACCTGTAATCCTAGCACTTTAGAAGGCCGAGGC AGAGCATAGCTTGTCTGGGTCTGGTGGCTCACTCCTGTAATCCTAGCACTTTAGAAGGCCGAGGC T A ZNF395,FBXO16 Ensembl:ENSG00000186918,Ensembl:ENSG00000214050 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs888889116 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87906,RMVar_hsa_circ_250983 41224 RMVar_ID_41224 Human_SNP_ID_357290720 A-to-I Human chr8 - 28375380 28375380 28375380 TCTCTCTCTCTCTTTTTTTTTTTTTTTTAGACAGTCTTGCACTGTTTCCTAGGCTGGAGTGCAGT TCTCTCTCTCTCTTTTTTTTTTTTTTTTAGACCGTCTTGCACTGTTTCCTAGGCTGGAGTGCAGT T G ZNF395,FBXO16 Ensembl:ENSG00000186918,Ensembl:ENSG00000214050 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1293669858 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_962098 RMVar_hsa_circ_87906,RMVar_hsa_circ_250983 41225 RMVar_ID_41225 Human_SNP_ID_357290908 A-to-I Human chr8 - 28376086 28376086 28376086 CCTGCAGTTGCAGCTACTTGGGAGGCTGAGGAAGGAGGATCACCTGAACCCGGGGAGGTTAAGGC CCTGCAGTTGCAGCTACTTGGGAGGCTGAGGACGGAGGATCACCTGAACCCGGGGAGGTTAAGGC T G ZNF395,FBXO16 Ensembl:ENSG00000186918,Ensembl:ENSG00000214050 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs565151238 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87906,RMVar_hsa_circ_250983 41226 RMVar_ID_41226 Human_SNP_ID_357290993 A-to-I Human chr8 - 28376425 28376425 28376425 TTTAGTGGAGATGGGGTTTCACCATGATGGCCAGGCTGGTCTTGAACTGACCTCAGGTGATCCTC TTTAGTGGAGATGGGGTTTCACCATGATGGCCCGGCTGGTCTTGAACTGACCTCAGGTGATCCTC T G ZNF395,FBXO16 Ensembl:ENSG00000186918,Ensembl:ENSG00000214050 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1403717169 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87906,RMVar_hsa_circ_250983 41227 RMVar_ID_41227 Human_SNP_ID_357307015 A-to-I Human chr8 - 28439648 28439648 28439648 TCAACAACTCCCAGAGCTCAGGGGATCCTCCCACCTCAGCCTCCCAGGTAGCCGGGACCTGTGCA TCAACAACTCCCAGAGCTCAGGGGATCCTCCCGCCTCAGCCTCCCAGGTAGCCGGGACCTGTGCA T C FBXO16 Ensembl:ENSG00000214050 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1303384927 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77970,RMVar_hsa_circ_87906,RMVar_hsa_circ_250983,RMVar_hsa_circ_250984 41228 RMVar_ID_41228 Human_SNP_ID_357312279 A-to-I Human chr8 - 28459535 28459535 28459535 GCTCACTGCAACCTCCGCCCACCCCGGGTTCAAGCAATTCTCTTGCCTCAGCCTCCCGAGTAGCT GCTCACTGCAACCTCCGCCCACCCCGGGTTCAGGCAATTCTCTTGCCTCAGCCTCCCGAGTAGCT T C FBXO16 Ensembl:ENSG00000214050 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs937226007 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35385,RMVar_hsa_circ_77970,RMVar_hsa_circ_87906,RMVar_hsa_circ_250983,RMVar_hsa_circ_350846,RMVar_hsa_circ_250984 41229 RMVar_ID_41229 Human_SNP_ID_357312717 A-to-I Human chr8 - 28460704 28460704 28460704 AGTCAGGTCGGCCAGGCGCAGAGGTGGCTCACACCTGTAATCCTAGCACTTTAAGAGGCCAAGGT AGTCAGGTCGGCCAGGCGCAGAGGTGGCTCACTCCTGTAATCCTAGCACTTTAAGAGGCCAAGGT T A FBXO16 Ensembl:ENSG00000214050 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1269845626 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35385,RMVar_hsa_circ_77970,RMVar_hsa_circ_87906,RMVar_hsa_circ_250983,RMVar_hsa_circ_350846,RMVar_hsa_circ_250984 41230 RMVar_ID_41230 Human_SNP_ID_357389210 A-to-I Human chr8 - 28771936 28771936 28771936 ACATCACTTGAGCCCAGGAGGTTGAGGTTGCAATGAGCTATGATCACACCACCACACTCCAGCCT ACATCACTTGAGCCCAGGAGGTTGAGGTTGCAGTGAGCTATGATCACACCACCACACTCCAGCCT T C INTS9 Ensembl:ENSG00000104299 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs535169286 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21364,RMVar_hsa_circ_251026,RMVar_hsa_circ_94615 41231 RMVar_ID_41231 Human_SNP_ID_357389858 A-to-I Human chr8 - 28773896 28773896 28773896 AATTGCTTGAACCGGGAGGCAGAGGTTGCAGTAAGCCAAGATCATGCCACCGCACTCCTACGTGG AATTGCTTGAACCGGGAGGCAGAGGTTGCAGTGAGCCAAGATCATGCCACCGCACTCCTACGTGG T C INTS9 Ensembl:ENSG00000104299 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1384721140 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21364,RMVar_hsa_circ_251026,RMVar_hsa_circ_94615 41232 RMVar_ID_41232 Human_SNP_ID_357389862 A-to-I Human chr8 - 28773908 28773908 28773908 GCTGTGGCAGAGAATTGCTTGAACCGGGAGGCAGAGGTTGCAGTAAGCCAAGATCATGCCACCGC GCTGTGGCAGAGAATTGCTTGAACCGGGAGGCGGAGGTTGCAGTAAGCCAAGATCATGCCACCGC T C INTS9 Ensembl:ENSG00000104299 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1262676298 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21364,RMVar_hsa_circ_251026,RMVar_hsa_circ_94615 41233 RMVar_ID_41233 Human_SNP_ID_357422697 A-to-I Human chr8 + 28911545 28911545 28911545 GCCCTGCTAATTTTTGTATTTTTAGTAGAGACAGGATTTCACCACATTGGCCAGACTGATCTTGA GCCCTGCTAATTTTTGTATTTTTAGTAGAGACGGGATTTCACCACATTGGCCAGACTGATCTTGA A G HMBOX1 Ensembl:ENSG00000147421 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1164361009 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_251039,RMVar_hsa_circ_95407 41234 RMVar_ID_41234 Human_SNP_ID_357426500 A-to-I Human chr8 + 28926701 28926701 28926701 GTGACCCTCCTGCCTCAGCTTCCTAAGTAGCTAGGACTACAAGTGTATACCACCATGCCTAGCTA GTGACCCTCCTGCCTCAGCTTCCTAAGTAGCTGGGACTACAAGTGTATACCACCATGCCTAGCTA A G HMBOX1 Ensembl:ENSG00000147421 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1211939204 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_251039,RMVar_hsa_circ_95407,RMVar_hsa_circ_321120 41235 RMVar_ID_41235 Human_SNP_ID_357432376 A-to-I Human chr8 + 28951912 28951912 28951912 AAACCAGGCTGAGCACGGTGGCTCCCACCTGTAATCCCAGCACTTTAAGAGGCCAAGGGAGGAGG AAACCAGGCTGAGCACGGTGGCTCCCACCTGTGATCCCAGCACTTTAAGAGGCCAAGGGAGGAGG A G HMBOX1-IT1,HMBOX1 Ensembl:ENSG00000259196,Ensembl:ENSG00000147421 lincRNA,Protein coding intron,intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs951792917 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_251039,RMVar_hsa_circ_95407,RMVar_hsa_circ_321120 41236 RMVar_ID_41236 Human_SNP_ID_357432410 A-to-I Human chr8 + 28952037 28952037 28952037 TCTACAAAAATTTTTTTAAAAATCAGCTGGGCATTATGGCATGTGCCTGTAGTCCCAGCTACTCT TCTACAAAAATTTTTTTAAAAATCAGCTGGGCGTTATGGCATGTGCCTGTAGTCCCAGCTACTCT A G HMBOX1-IT1,HMBOX1 Ensembl:ENSG00000259196,Ensembl:ENSG00000147421 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1323087158 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_251039,RMVar_hsa_circ_95407,RMVar_hsa_circ_321120 41237 RMVar_ID_41237 Human_SNP_ID_357439629 A-to-I Human chr8 + 28982112 28982112 28982112 ACAAAAAGCCAGGCGTGGTGGCGGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGTGGGAGA ACAAAAAGCCAGGCGTGGTGGCGGGCGCCTGTGGTCCCAGCTACTCGGGAGGCTGAGGTGGGAGA A G HMBOX1 Ensembl:ENSG00000147421 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1271351121 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_30212,RMVar_hsa_circ_251039,RMVar_hsa_circ_95407,RMVar_hsa_circ_286914,RMVar_hsa_circ_354511,RMVar_hsa_circ_278479,RMVar_hsa_circ_251040,RMVar_hsa_circ_251041,RMVar_hsa_circ_251046,RMVar_hsa_circ_279498,RMVar_hsa_circ_301173,RMVar_hsa_circ_251047,RMVar_hsa_circ_284878,RMVar_hsa_circ_251049,RMVar_hsa_circ_251050 41238 RMVar_ID_41238 Human_SNP_ID_150652712 A-to-I Human chr3 - 120056407 120056407 120056407 TGAACCTGGAAGGTGGAGGTTGCAGTCAGCCAAGATCGTACTAGTGCATCTCCAGCCTGGACAAC TGAACCTGGAAGGTGGAGGTTGCAGTCAGCCACGATCGTACTAGTGCATCTCCAGCCTGGACAAC T G GSK3B Ensembl:ENSG00000082701 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs994766607 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 41239 RMVar_ID_41239 Human_SNP_ID_150652721 A-to-I Human chr3 - 120056436 120056436 120056436 ACGTGGGAGGCTGAGGCAGGAGAATCACTTGAACCTGGAAGGTGGAGGTTGCAGTCAGCCAAGAT ACGTGGGAGGCTGAGGCAGGAGAATCACTTGACCCTGGAAGGTGGAGGTTGCAGTCAGCCAAGAT T G GSK3B Ensembl:ENSG00000082701 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1477273957 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 41240 RMVar_ID_41240 Human_SNP_ID_150656952 A-to-I Human chr3 - 120074079 120074079 120074079 GCTGGTCTTGAACTCCTAGACTCAAGTGATCTATCCACCTCGGCCTCCCATAGTGCTGGGATTAC GCTGGTCTTGAACTCCTAGACTCAAGTGATCTGTCCACCTCGGCCTCCCATAGTGCTGGGATTAC T C GSK3B Ensembl:ENSG00000082701 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1056451840 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 41241 RMVar_ID_41241 Human_SNP_ID_150660421 A-to-I Human chr3 - 120087276 120087276 120087276 TTCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAACCACCACATGTGGCCGAACTAA TTCCCACCTCGGCCTCCCAAAGTGCTGGGATTGCAGGCGTGAACCACCACATGTGGCCGAACTAA T C GSK3B Ensembl:ENSG00000082701 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1415110387 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 41242 RMVar_ID_41242 Human_SNP_ID_150660425 A-to-I Human chr3 - 120087289 120087289 120087289 TGACCTTGTGATCTTCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAACCACCACAT TGACCTTGTGATCTTCCCACCTCGGCCTCCCAGAGTGCTGGGATTACAGGCGTGAACCACCACAT T C GSK3B Ensembl:ENSG00000082701 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005002864 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 41243 RMVar_ID_41243 Human_SNP_ID_150660431 A-to-I Human chr3 - 120087303 120087303 120087303 TGGTCTCAAAATCCTGACCTTGTGATCTTCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGC TGGTCTCAAAATCCTGACCTTGTGATCTTCCCTCCTCGGCCTCCCAAAGTGCTGGGATTACAGGC T A GSK3B Ensembl:ENSG00000082701 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1034066785 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 41244 RMVar_ID_41244 Human_SNP_ID_150660478 A-to-I Human chr3 - 120087493 120087493 120087493 GAGTCTCGCACTGTTTCCTGGGCTGGAGTGCCATGGCGTGATCTGGGCTTACTGCAACCTCTGCC GAGTCTCGCACTGTTTCCTGGGCTGGAGTGCCGTGGCGTGATCTGGGCTTACTGCAACCTCTGCC T C GSK3B Ensembl:ENSG00000082701 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1559908206 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14581110,Human_RBP_ID_17573805 RMVar_hsa_circ_377669,RMVar_hsa_circ_220517,RMVar_hsa_circ_264817,RMVar_hsa_circ_378604,RMVar_hsa_circ_220522 41245 RMVar_ID_41245 Human_SNP_ID_150663300 A-to-I Human chr3 + 120096869 120096869 120096869 GTTGGTCAGGCTGGTCTCGAACTCCCGACCTCAGGTGATCTGCCTGCCTCAGCCTCACAGAGTGT GTTGGTCAGGCTGGTCTCGAACTCCCGACCTCTGGTGATCTGCCTGCCTCAGCCTCACAGAGTGT A T AC092910.3 Ensembl:ENSG00000242622 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs557465719 Functional Loss SNV dbSNP153 33..33 33 - - - 41246 RMVar_ID_41246 Human_SNP_ID_150663305 A-to-I Human chr3 + 120096887 120096887 120096887 GAACTCCCGACCTCAGGTGATCTGCCTGCCTCAGCCTCACAGAGTGTCAGGATTACAGGCGTAAG GAACTCCCGACCTCAGGTGATCTGCCTGCCTCCGCCTCACAGAGTGTCAGGATTACAGGCGTAAG A C AC092910.3 Ensembl:ENSG00000242622 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1030440967 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23188268 41247 RMVar_ID_41247 Human_SNP_ID_150663306 A-to-I Human chr3 + 120096887 120096887 120096887 GAACTCCCGACCTCAGGTGATCTGCCTGCCTCAGCCTCACAGAGTGTCAGGATTACAGGCGTAAG GAACTCCCGACCTCAGGTGATCTGCCTGCCTCGGCCTCACAGAGTGTCAGGATTACAGGCGTAAG A G AC092910.3 Ensembl:ENSG00000242622 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1030440967 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23188268 41248 RMVar_ID_41248 Human_SNP_ID_150663386 A-to-I Human chr3 + 120097201 120097201 120097201 TAAAACTTAGCTGGGCGTGGTGGCGGGCGTCTATAATACCAGTTACTTGGGAGGCTGAGGCAGGA TAAAACTTAGCTGGGCGTGGTGGCGGGCGTCTGTAATACCAGTTACTTGGGAGGCTGAGGCAGGA A G AC092910.3 Ensembl:ENSG00000242622 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs555349541 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25690046 41249 RMVar_ID_41249 Human_SNP_ID_150663387 A-to-I Human chr3 + 120097203 120097203 120097203 AAACTTAGCTGGGCGTGGTGGCGGGCGTCTATAATACCAGTTACTTGGGAGGCTGAGGCAGGATA AAACTTAGCTGGGCGTGGTGGCGGGCGTCTATGATACCAGTTACTTGGGAGGCTGAGGCAGGATA A G AC092910.3 Ensembl:ENSG00000242622 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs957880915 Functional Loss SNV dbSNP153 33..33 33 - - - 41250 RMVar_ID_41250 Human_SNP_ID_150663557 A-to-I Human chr3 + 120097890 120097884 120097890 TAATCTCACTGTTATCCAGGATGGAGTGCAGTAGCACAGTCATAGCTCACTATGGCCTTGAACTT TAATCTCACTGTTATCCAGGATGGAGT______GCACAGTCATAGCTCACTATGGCCTTGAACTT TGCAGTA T AC092910.3 Ensembl:ENSG00000242622 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs758528595 Functional Loss DEL dbSNP153 28..33 33 - - - 41251 RMVar_ID_41251 Human_SNP_ID_150663560 A-to-I Human chr3 + 120097906 120097906 120097906 CAGGATGGAGTGCAGTAGCACAGTCATAGCTCACTATGGCCTTGAACTTCTGGGCTCAAGCAGTC CAGGATGGAGTGCAGTAGCACAGTCATAGCTCGCTATGGCCTTGAACTTCTGGGCTCAAGCAGTC A G AC092910.3 Ensembl:ENSG00000242622 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749991275 Functional Loss SNV dbSNP153 33..33 33 - - - 41252 RMVar_ID_41252 Human_SNP_ID_150663952 A-to-I Human chr3 + 120099631 120099626 120099631 GCTGGAGTGCAATGGCGTGATCTCGGCTCACCACAACCTCCACCTCCCAGGTTCAAGCAATTCTG GCTGGAGTGCAATGGCGTGATCTCGGCT_____CAACCTCCACCTCCCAGGTTCAAGCAATTCTG TCACCA T AC092910.3 Ensembl:ENSG00000242622 lincRNA intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs921122403 Functional Loss DEL dbSNP153 29..33 33 - - - 41253 RMVar_ID_41253 Human_SNP_ID_150663972 A-to-I Human chr3 + 120099692 120099692 120099692 TCTGCCTCAGCCTCCCGAGTAGCTGAGATTACAGGCATGCGCCACCACGCCCGGCTAATTTTGTG TCTGCCTCAGCCTCCCGAGTAGCTGAGATTACCGGCATGCGCCACCACGCCCGGCTAATTTTGTG A C AC092910.3 Ensembl:ENSG00000242622 lincRNA intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1324959944 Functional Loss SNV dbSNP153 33..33 33 - - - 41254 RMVar_ID_41254 Human_SNP_ID_150665207 A-to-I Human chr3 + 120104895 120104895 120104895 GAAAAAGAGTTCGAGACCAGCCTGGGCAACATAGTGAGACCCTCTCTCTCAAAAAAAATAGCCAA GAAAAAGAGTTCGAGACCAGCCTGGGCAACATGGTGAGACCCTCTCTCTCAAAAAAAATAGCCAA A G AC092910.3 Ensembl:ENSG00000242622 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1451266994 Functional Loss SNV dbSNP153 33..33 33 - - - 41255 RMVar_ID_41255 Human_SNP_ID_150711219 A-to-I Human chr3 + 120307435 120307435 120307435 TCACTACTCGCAAGCAAGCAGTGGGACCTGGTAGTGTCAACTCAGGCCCAGTCCAGATCGTCAAC TCACTACTCGCAAGCAAGCAGTGGGACCTGGTGGTGTCAACTCAGGCCCAGTCCAGATCGTCAAC A G AC063952.2 Ensembl:ENSG00000240882 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1219784903 Functional Loss SNV dbSNP153 33..33 33 - - - 41256 RMVar_ID_41256 Human_SNP_ID_150718885 A-to-I Human chr3 - 120339999 120339999 120339999 AAAATTAGCCAGGCGTGGTGGCGGGCGCCTGTAATCCCAACTACTCGGGAGGCTGAGGTAGAATT AAAATTAGCCAGGCGTGGTGGCGGGCGCCTGTCATCCCAACTACTCGGGAGGCTGAGGTAGAATT T G LRRC58 Ensembl:ENSG00000163428 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1289111058 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_220527,RMVar_hsa_circ_120010,RMVar_hsa_circ_220528 41257 RMVar_ID_41257 Human_SNP_ID_150719043 A-to-I Human chr3 - 120340707 120340707 120340707 TTTGTTTGTTTGTTTGTTTTTGTTTTTTTAGTAGAGACGGTATTTTACCAGTTAGCCAAGCTGGT TTTGTTTGTTTGTTTGTTTTTGTTTTTTTAGTGGAGACGGTATTTTACCAGTTAGCCAAGCTGGT T C LRRC58 Ensembl:ENSG00000163428 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1282695493 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7109256 RMVar_hsa_circ_220527,RMVar_hsa_circ_120010,RMVar_hsa_circ_220528 41258 RMVar_ID_41258 Human_SNP_ID_150720253 A-to-I Human chr3 - 120346085 120346085 120346085 GCCAGCTAATTTTTGTACTTTTAGTAGAGACAAAGTTTCACCATGTTGGCCAGGCCAGGCTGGTC GCCAGCTAATTTTTGTACTTTTAGTAGAGACAGAGTTTCACCATGTTGGCCAGGCCAGGCTGGTC T C LRRC58 Ensembl:ENSG00000163428 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935878380 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_220527,RMVar_hsa_circ_120010,RMVar_hsa_circ_220528 41259 RMVar_ID_41259 Human_SNP_ID_150720254 A-to-I Human chr3 - 120346085 120346085 120346085 GCCAGCTAATTTTTGTACTTTTAGTAGAGACAAAGTTTCACCATGTTGGCCAGGCCAGGCTGGTC GCCAGCTAATTTTTGTACTTTTAGTAGAGACACAGTTTCACCATGTTGGCCAGGCCAGGCTGGTC T G LRRC58 Ensembl:ENSG00000163428 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935878380 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_220527,RMVar_hsa_circ_120010,RMVar_hsa_circ_220528 41260 RMVar_ID_41260 Human_SNP_ID_150733343 A-to-I Human chr3 - 120403257 120403257 120403257 AAGAGTTTCTCAAGTGCCTCAACCCATCTTTCAACCCTCCTGAGAAGAGTATGCCTAACCTAAGA AAGAGTTTCTCAAGTGCCTCAACCCATCTTTCCACCCTCCTGAGAAGAGTATGCCTAACCTAAGA T G FSTL1 Ensembl:ENSG00000163430 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs748455860 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_68231,Human_RBP_ID_587093,Human_RBP_ID_3683005,Human_RBP_ID_7109405,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 41261 RMVar_ID_41261 Human_SNP_ID_150866317 A-to-I Human chr3 + 120961336 120961336 120961336 TAGGGTACACGTGCACAACGTGCAGGTTTGATACATAGGTATACGTGTACCATGTTTGTAGCTGC TAGGGTACACGTGCACAACGTGCAGGTTTGATGCATAGGTATACGTGTACCATGTTTGTAGCTGC A G STXBP5L Ensembl:ENSG00000145087 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs557717765 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14263,RMVar_hsa_circ_24755,RMVar_hsa_circ_37822,RMVar_hsa_circ_327959,RMVar_hsa_circ_362837,RMVar_hsa_circ_267726 41262 RMVar_ID_41262 Human_SNP_ID_150866954 A-to-I Human chr3 + 120962991 120962991 120962991 GGTTTGTAGTTCTTCTTCAAGAAGTCCTTCACATCCCTTGTTAGTTGGATTCCTAGGTATTTTAT GGTTTGTAGTTCTTCTTCAAGAAGTCCTTCACGTCCCTTGTTAGTTGGATTCCTAGGTATTTTAT A G STXBP5L Ensembl:ENSG00000145087 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1212179873 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14263,RMVar_hsa_circ_24755,RMVar_hsa_circ_37822,RMVar_hsa_circ_327959,RMVar_hsa_circ_362837,RMVar_hsa_circ_267726 41263 RMVar_ID_41263 Human_SNP_ID_150879421 A-to-I Human chr3 + 120992928 120992927 120992929 TATACTAATTTACACTGCCGCCACCCGTGTATAAGAGTTCCTTTTCTCCACATCCTTGCCAGTAT TATACTAATTTACACTGCCGCCACCCGTGTAT__GAGTTCCTTTTCTCCACATCCTTGCCAGTAT TAA T STXBP5L Ensembl:ENSG00000145087 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1418272974 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_14263,RMVar_hsa_circ_24755,RMVar_hsa_circ_37822,RMVar_hsa_circ_327959,RMVar_hsa_circ_362837,RMVar_hsa_circ_267726 41264 RMVar_ID_41264 Human_SNP_ID_150879422 A-to-I Human chr3 + 120992928 120992928 120992928 TATACTAATTTACACTGCCGCCACCCGTGTATAAGAGTTCCTTTTCTCCACATCCTTGCCAGTAT TATACTAATTTACACTGCCGCCACCCGTGTATTAGAGTTCCTTTTCTCCACATCCTTGCCAGTAT A T STXBP5L Ensembl:ENSG00000145087 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1380008631 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14263,RMVar_hsa_circ_24755,RMVar_hsa_circ_37822,RMVar_hsa_circ_327959,RMVar_hsa_circ_362837,RMVar_hsa_circ_267726 41265 RMVar_ID_41265 Human_SNP_ID_150879608 A-to-I Human chr3 + 120993452 120993452 120993452 TTCTAGTATTTTCAGTTCCAGGTCTTATGTTTAAGGCTTTAAGCATTTGGAGTTGAGTTTTGCGT TTCTAGTATTTTCAGTTCCAGGTCTTATGTTTGAGGCTTTAAGCATTTGGAGTTGAGTTTTGCGT A G STXBP5L Ensembl:ENSG00000145087 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs150586078 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14263,RMVar_hsa_circ_24755,RMVar_hsa_circ_37822,RMVar_hsa_circ_327959,RMVar_hsa_circ_362837,RMVar_hsa_circ_267726 41266 RMVar_ID_41266 Human_SNP_ID_150879609 A-to-I Human chr3 + 120993452 120993452 120993452 TTCTAGTATTTTCAGTTCCAGGTCTTATGTTTAAGGCTTTAAGCATTTGGAGTTGAGTTTTGCGT TTCTAGTATTTTCAGTTCCAGGTCTTATGTTTTAGGCTTTAAGCATTTGGAGTTGAGTTTTGCGT A T STXBP5L Ensembl:ENSG00000145087 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs150586078 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14263,RMVar_hsa_circ_24755,RMVar_hsa_circ_37822,RMVar_hsa_circ_327959,RMVar_hsa_circ_362837,RMVar_hsa_circ_267726 41267 RMVar_ID_41267 Human_SNP_ID_150879741 A-to-I Human chr3 + 120993729 120993729 120993729 ATATTGCCTTGTAATATATTTTGACATCAGGTAGTGTGATGCTTCCAGCTTTGTTCTTTTTCTTT ATATTGCCTTGTAATATATTTTGACATCAGGTGGTGTGATGCTTCCAGCTTTGTTCTTTTTCTTT A G STXBP5L Ensembl:ENSG00000145087 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1052565470 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14263,RMVar_hsa_circ_24755,RMVar_hsa_circ_37822,RMVar_hsa_circ_327959,RMVar_hsa_circ_362837,RMVar_hsa_circ_267726 41268 RMVar_ID_41268 Human_SNP_ID_150879742 A-to-I Human chr3 + 120993729 120993729 120993729 ATATTGCCTTGTAATATATTTTGACATCAGGTAGTGTGATGCTTCCAGCTTTGTTCTTTTTCTTT ATATTGCCTTGTAATATATTTTGACATCAGGTTGTGTGATGCTTCCAGCTTTGTTCTTTTTCTTT A T STXBP5L Ensembl:ENSG00000145087 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1052565470 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14263,RMVar_hsa_circ_24755,RMVar_hsa_circ_37822,RMVar_hsa_circ_327959,RMVar_hsa_circ_362837,RMVar_hsa_circ_267726 41269 RMVar_ID_41269 Human_SNP_ID_150879828 A-to-I Human chr3 + 120993938 120993938 120993938 ATAATAATTCTTCCAATTCATGAGCATGGGATATGTTTCCATCTGTTTGTGTCCTCTTAAATTTC ATAATAATTCTTCCAATTCATGAGCATGGGATGTGTTTCCATCTGTTTGTGTCCTCTTAAATTTC A G STXBP5L Ensembl:ENSG00000145087 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1355098356 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14263,RMVar_hsa_circ_24755,RMVar_hsa_circ_37822,RMVar_hsa_circ_327959,RMVar_hsa_circ_362837,RMVar_hsa_circ_267726 41270 RMVar_ID_41270 Human_SNP_ID_150919094 A-to-I Human chr3 + 121098496 121098496 121098496 TGTCCTCATGATAATGAGTGAGTTCTGACTCTATAAGATTAGTCATCAAGGCAGAGAGATCTGCC TGTCCTCATGATAATGAGTGAGTTCTGACTCTCTAAGATTAGTCATCAAGGCAGAGAGATCTGCC A C STXBP5L Ensembl:ENSG00000145087 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1016635219 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14263,RMVar_hsa_circ_24755,RMVar_hsa_circ_36041,RMVar_hsa_circ_37822,RMVar_hsa_circ_327959,RMVar_hsa_circ_362837,RMVar_hsa_circ_267381,RMVar_hsa_circ_342884,RMVar_hsa_circ_75821,RMVar_hsa_circ_67114,RMVar_hsa_circ_220557,RMVar_hsa_circ_303606 41271 RMVar_ID_41271 Human_SNP_ID_150919095 A-to-I Human chr3 + 121098496 121098496 121098496 TGTCCTCATGATAATGAGTGAGTTCTGACTCTATAAGATTAGTCATCAAGGCAGAGAGATCTGCC TGTCCTCATGATAATGAGTGAGTTCTGACTCTGTAAGATTAGTCATCAAGGCAGAGAGATCTGCC A G STXBP5L Ensembl:ENSG00000145087 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1016635219 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14263,RMVar_hsa_circ_24755,RMVar_hsa_circ_36041,RMVar_hsa_circ_37822,RMVar_hsa_circ_327959,RMVar_hsa_circ_362837,RMVar_hsa_circ_267381,RMVar_hsa_circ_342884,RMVar_hsa_circ_75821,RMVar_hsa_circ_67114,RMVar_hsa_circ_220557,RMVar_hsa_circ_303606 41272 RMVar_ID_41272 Human_SNP_ID_150935470 A-to-I Human chr3 + 121160453 121160453 121160453 AAAATAATACAAATAAAAAGAAACAATACAGTATCACAACTATTTGCATAGTGTCACACTGTATT AAAATAATACAAATAAAAAGAAACAATACAGTGTCACAACTATTTGCATAGTGTCACACTGTATT A G STXBP5L Ensembl:ENSG00000145087 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1427005111 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8556333 RMVar_hsa_circ_14263,RMVar_hsa_circ_24755,RMVar_hsa_circ_13123,RMVar_hsa_circ_36041,RMVar_hsa_circ_37822,RMVar_hsa_circ_267381,RMVar_hsa_circ_75821,RMVar_hsa_circ_67114,RMVar_hsa_circ_220557,RMVar_hsa_circ_26935,RMVar_hsa_circ_5445,RMVar_hsa_circ_319025,RMVar_hsa_circ_315720,RMVar_hsa_circ_270765,RMVar_hsa_circ_288397,RMVar_hsa_circ_48610,RMVar_hsa_circ_28493,RMVar_hsa_circ_220561,RMVar_hsa_circ_220562,RMVar_hsa_circ_333394,RMVar_hsa_circ_277265,RMVar_hsa_circ_220563 41273 RMVar_ID_41273 Human_SNP_ID_150955754 A-to-I Human chr3 + 121228811 121228811 121228811 AGGCAGAAGAATCGCTTGAACCTGAAAGGTGGAAGTTCCAGTGAGCCGAGATCATGCCACTGCAC AGGCAGAAGAATCGCTTGAACCTGAAAGGTGGCAGTTCCAGTGAGCCGAGATCATGCCACTGCAC A C STXBP5L Ensembl:ENSG00000145087 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1419357219 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6577,RMVar_hsa_circ_14263,RMVar_hsa_circ_24755,RMVar_hsa_circ_36041,RMVar_hsa_circ_37822,RMVar_hsa_circ_267381,RMVar_hsa_circ_75821,RMVar_hsa_circ_67114,RMVar_hsa_circ_220557,RMVar_hsa_circ_26935,RMVar_hsa_circ_5445,RMVar_hsa_circ_319025,RMVar_hsa_circ_315720,RMVar_hsa_circ_270765,RMVar_hsa_circ_48610,RMVar_hsa_circ_28493,RMVar_hsa_circ_220561,RMVar_hsa_circ_220562,RMVar_hsa_circ_333394,RMVar_hsa_circ_277265,RMVar_hsa_circ_308698,RMVar_hsa_circ_220563,RMVar_hsa_circ_310360,RMVar_hsa_circ_38111,RMVar_hsa_circ_53176,RMVar_hsa_circ_288376,RMVar_hsa_circ_220564,RMVar_hsa_circ_270462,RMVar_hsa_circ_220565,RMVar_hsa_circ_220566 41274 RMVar_ID_41274 Human_SNP_ID_150979151 A-to-I Human chr3 + 121322432 121322432 121322432 CCCAAGAGGCGGAGGTTGTGGTGAGCTGAGATAGTACCATTGCACTCCAGCCTGGGCAACAAGAG CCCAAGAGGCGGAGGTTGTGGTGAGCTGAGATGGTACCATTGCACTCCAGCCTGGGCAACAAGAG A G STXBP5L Ensembl:ENSG00000145087 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs969218808 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36041,RMVar_hsa_circ_16237,RMVar_hsa_circ_324355,RMVar_hsa_circ_220569,RMVar_hsa_circ_377622 41275 RMVar_ID_41275 Human_SNP_ID_151004425 A-to-I Human chr3 - 121405448 121405446 121405448 ATTCTATGTGCTCTAGGCTCTATTTTAGTCATAGTCAATATAGTGGTGAATAAAACAGACAAAAG ATTCTATGTGCTCTAGGCTCTATTTTAGTCATGGGCAATATAGTGGTGAATAAAACAGACAAAAG ACT CCC AC079841.2 Ensembl:ENSG00000287022 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs386665196 Functional Loss MNV dbSNP153 33..35 33 - - - 41276 RMVar_ID_41276 Human_SNP_ID_151026803 A-to-I Human chr3 - 121496313 121496313 121496313 AAATTAGCCAGGTGTGGCGGTGGGCGCTTATAATCCCAGCTACTGGGGAGGCTGAGGCAGAGAAT AAATTAGCCAGGTGTGGCGGTGGGCGCTTATAGTCCCAGCTACTGGGGAGGCTGAGGCAGAGAAT T C POLQ Ensembl:ENSG00000051341 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1490168927 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2779,RMVar_hsa_circ_27189,RMVar_hsa_circ_327602,RMVar_hsa_circ_362003,RMVar_hsa_circ_48738,RMVar_hsa_circ_65070,RMVar_hsa_circ_111632,RMVar_hsa_circ_220587,RMVar_hsa_circ_375259,RMVar_hsa_circ_220588,RMVar_hsa_circ_101118,RMVar_hsa_circ_51898,RMVar_hsa_circ_220590,RMVar_hsa_circ_52289,RMVar_hsa_circ_349455,RMVar_hsa_circ_116364,RMVar_hsa_circ_220593,RMVar_hsa_circ_220592,RMVar_hsa_circ_363212,RMVar_hsa_circ_58205,RMVar_hsa_circ_373704,RMVar_hsa_circ_55914,RMVar_hsa_circ_315647,RMVar_hsa_circ_220594,RMVar_hsa_circ_297761,RMVar_hsa_circ_220595 41277 RMVar_ID_41277 Human_SNP_ID_151029959 A-to-I Human chr3 - 121510203 121510203 121510203 TGGTGGAGTGGCAAGTACATCACAAGATATGCATACTTATGCTGCCTGCACATTTTTGGCTGCAA TGGTGGAGTGGCAAGTACATCACAAGATATGCGTACTTATGCTGCCTGCACATTTTTGGCTGCAA T C POLQ Ensembl:ENSG00000051341 Protein coding CDS GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1480430392 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14584883,Human_RBP_ID_18794865 Human_Splice_Rec_472404,Human_Splice_Rec_472462 RMVar_hsa_circ_2779,RMVar_hsa_circ_27189,RMVar_hsa_circ_48738,RMVar_hsa_circ_65070,RMVar_hsa_circ_111632,RMVar_hsa_circ_220588,RMVar_hsa_circ_51898,RMVar_hsa_circ_52289,RMVar_hsa_circ_58205,RMVar_hsa_circ_51436,RMVar_hsa_circ_55914,RMVar_hsa_circ_339021,RMVar_hsa_circ_92313,RMVar_hsa_circ_9179,RMVar_hsa_circ_23529,RMVar_hsa_circ_220598 41278 RMVar_ID_41278 Human_SNP_ID_151063299 A-to-I Human chr3 - 121638159 121638159 121638159 TACTCAGGAGGATTGCTTGACCCCAGGAGTTCAAGGTTACAGTGAGCCATGATTGTACTCTGCAC TACTCAGGAGGATTGCTTGACCCCAGGAGTTCGAGGTTACAGTGAGCCATGATTGTACTCTGCAC T C HCLS1 Ensembl:ENSG00000180353 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1231683864 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66403,RMVar_hsa_circ_88228,RMVar_hsa_circ_91167,RMVar_hsa_circ_220603,RMVar_hsa_circ_220604,RMVar_hsa_circ_56671 41279 RMVar_ID_41279 Human_SNP_ID_151098664 A-to-I Human chr3 - 121784901 121784901 121784901 GGGAGGCTGAGGCGGGAGGATCACTTGAGCTCAGGAGTTTGAGACCAGCTTAGGACACATAATAA GGGAGGCTGAGGCGGGAGGATCACTTGAGCTCGGGAGTTTGAGACCAGCTTAGGACACATAATAA T C IQCB1 Ensembl:ENSG00000173226 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1477897710 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19939,RMVar_hsa_circ_366967,RMVar_hsa_circ_322598,RMVar_hsa_circ_377877,RMVar_hsa_circ_48572,RMVar_hsa_circ_220624 41280 RMVar_ID_41280 Human_SNP_ID_151109008 A-to-I Human chr3 - 121830002 121829994 121830002 GGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGACCGCAAGTGATTCACCCACCTTGGC GGGTTTCACCATGTTGGCCAGGCTGGTCTTGA________CCGCAAGTGATTCACCCACCTTGGC GTCAGGAGT G IQCB1 Ensembl:ENSG00000173226 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1268751912 Functional Loss DEL dbSNP153 33..40 33 - - - Human_RBP_ID_14587241 41281 RMVar_ID_41281 Human_SNP_ID_151109019 A-to-I Human chr3 - 121830070 121830070 121830070 CTGAGTAACTGGGATTACAGGCACGCGCCACCATGCCCAGCTGATTTTTTGTATTCTTAGTAGAA CTGAGTAACTGGGATTACAGGCACGCGCCACCTTGCCCAGCTGATTTTTTGTATTCTTAGTAGAA T A IQCB1 Ensembl:ENSG00000173226 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs911495707 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25691311 41282 RMVar_ID_41282 Human_SNP_ID_151109037 A-to-I Human chr3 - 121830152 121830152 121830152 TCACTCAGGCTGGAGTGCAGTGATGTGATCTCAGGTCACTCAACCTCCACCTCCTAGGTTCAAGC TCACTCAGGCTGGAGTGCAGTGATGTGATCTCGGGTCACTCAACCTCCACCTCCTAGGTTCAAGC T C IQCB1 Ensembl:ENSG00000173226 Protein coding intron GSE38233;GSE100210;GSE99789 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 24183664,29129909,29796672 RNA-Seq:(High) rs993247000 Functional Loss SNV dbSNP153 33..33 33 - - - 41283 RMVar_ID_41283 Human_SNP_ID_151109753 A-to-I Human chr3 - 121833147 121833147 121833147 AGAGCTCTTACTATGTGCCAGGAATTGTTCCAATTGCTTTCATGTATTAACTCATTTAATCATCT AGAGCTCTTACTATGTGCCAGGAATTGTTCCAGTTGCTTTCATGTATTAACTCATTTAATCATCT T C IQCB1 Ensembl:ENSG00000173226 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1437154304 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17573812 41284 RMVar_ID_41284 Human_SNP_ID_151121287 A-to-I Human chr3 + 121881691 121881691 121881691 GCTGCCACACCCGGCTAATTTTTTTGTATTTTAGTAGAGATGGGGTTTCATTGTGTTGCCCAGGC GCTGCCACACCCGGCTAATTTTTTTGTATTTTGGTAGAGATGGGGTTTCATTGTGTTGCCCAGGC A G EAF2 Ensembl:ENSG00000145088 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1226013253 Functional Loss SNV dbSNP153 33..33 33 - - - 41285 RMVar_ID_41285 Human_SNP_ID_151225320 A-to-I Human chr3 + 122318388 122318388 122318388 ATAAGGATGGCTATAATGGATTTGGTAGTGATAGTGGTTATGAAGGAGGCAGCCCTAGTTACTCT ATAAGGATGGCTATAATGGATTTGGTAGTGATCGTGGTTATGAAGGAGGCAGCCCTAGTTACTCT A C HNRNPA1P23 Ensembl:ENSG00000240236 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1296072014 Functional Loss SNV dbSNP153 33..33 33 - - - 41286 RMVar_ID_41286 Human_SNP_ID_151225321 A-to-I Human chr3 + 122318388 122318388 122318388 ATAAGGATGGCTATAATGGATTTGGTAGTGATAGTGGTTATGAAGGAGGCAGCCCTAGTTACTCT ATAAGGATGGCTATAATGGATTTGGTAGTGATGGTGGTTATGAAGGAGGCAGCCCTAGTTACTCT A G HNRNPA1P23 Ensembl:ENSG00000240236 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1296072014 Functional Loss SNV dbSNP153 33..33 33 - - - 41287 RMVar_ID_41287 Human_SNP_ID_151237744 A-to-I Human chr3 - 122369888 122369877 122369889 AAAATTAGCTGGACGTAGTGGTGTGCGCCTATAGTCCCAGCTACCTGGGAGGCTAAGGCAGGAGG AAAATTAGCTGGACGTAGTGGTGTGCGCCTA____________CCTGGGAGGCTAAGGCAGGAGG GTAGCTGGGACTA G CCDC58 Ensembl:ENSG00000160124 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1471761003 Functional Loss DEL dbSNP153 32..43 33 - - - RMVar_hsa_circ_45947,RMVar_hsa_circ_355514 41288 RMVar_ID_41288 Human_SNP_ID_151237751 A-to-I Human chr3 - 122369888 122369888 122369888 AAAATTAGCTGGACGTAGTGGTGTGCGCCTATAGTCCCAGCTACCTGGGAGGCTAAGGCAGGAGG AAAATTAGCTGGACGTAGTGGTGTGCGCCTATGGTCCCAGCTACCTGGGAGGCTAAGGCAGGAGG T C CCDC58 Ensembl:ENSG00000160124 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs531758349 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45947,RMVar_hsa_circ_355514 41289 RMVar_ID_41289 Human_SNP_ID_151237752 A-to-I Human chr3 - 122369890 122369890 122369890 CAAAAATTAGCTGGACGTAGTGGTGTGCGCCTATAGTCCCAGCTACCTGGGAGGCTAAGGCAGGA CAAAAATTAGCTGGACGTAGTGGTGTGCGCCTGTAGTCCCAGCTACCTGGGAGGCTAAGGCAGGA T C CCDC58 Ensembl:ENSG00000160124 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs927687148 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45947,RMVar_hsa_circ_355514 41290 RMVar_ID_41290 Human_SNP_ID_151259427 A-to-I Human chr3 - 122457830 122457830 122457830 CACTTGCTCTCCAGGTGAGCCTGGCATTTGCTAGGAACCAGAGTGGAACCGGCAAAGTGGCCAGC CACTTGCTCTCCAGGTGAGCCTGGCATTTGCTGGGAACCAGAGTGGAACCGGCAAAGTGGCCAGC T C KPNA1 Ensembl:ENSG00000114030 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1355499938 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11145,Human_RBP_ID_19012877,Human_RBP_ID_25763091 Human_Splice_Rec_473464,Human_Splice_Rec_473486,Human_Splice_Rec_473512,Human_Splice_Rec_473540 RMVar_hsa_circ_1926,RMVar_hsa_circ_343784,RMVar_hsa_circ_358978,RMVar_hsa_circ_114079,RMVar_hsa_circ_220655,RMVar_hsa_circ_313593,RMVar_hsa_circ_220657,RMVar_hsa_circ_42916,RMVar_hsa_circ_220656,RMVar_hsa_circ_70006,RMVar_hsa_circ_309531,RMVar_hsa_circ_325129,RMVar_hsa_circ_378476,RMVar_hsa_circ_220658,RMVar_hsa_circ_281420 41291 RMVar_ID_41291 Human_SNP_ID_151259777 A-to-I Human chr3 - 122459554 122459554 122459554 GACTTTTCTCAGGATAAAAGGAAATCCAGACAACCAACACTGCAGAGAACAGAGCCTGATCCCCT GACTTTTCTCAGGATAAAAGGAAATCCAGACAGCCAACACTGCAGAGAACAGAGCCTGATCCCCT T C KPNA1 Ensembl:ENSG00000114030 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs962094212 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14589421,Human_RBP_ID_22676607,Human_RBP_ID_27822440 RMVar_hsa_circ_1926,RMVar_hsa_circ_343784,RMVar_hsa_circ_358978,RMVar_hsa_circ_114079,RMVar_hsa_circ_220655,RMVar_hsa_circ_313593,RMVar_hsa_circ_220657,RMVar_hsa_circ_42916,RMVar_hsa_circ_220656,RMVar_hsa_circ_70006,RMVar_hsa_circ_309531,RMVar_hsa_circ_325129,RMVar_hsa_circ_378476,RMVar_hsa_circ_220658,RMVar_hsa_circ_281420 41292 RMVar_ID_41292 Human_SNP_ID_151266785 A-to-I Human chr3 - 122488459 122488459 122488459 GCTAGAGTGTAGTGGTGTGATTACAACTCACTATAGCCTCAACCTCCCAGACTCAAAGTGATTCA GCTAGAGTGTAGTGGTGTGATTACAACTCACTGTAGCCTCAACCTCCCAGACTCAAAGTGATTCA T C KPNA1 Ensembl:ENSG00000114030 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474102285 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2743956,Human_RBP_ID_3683791 RMVar_hsa_circ_42916,RMVar_hsa_circ_63811,RMVar_hsa_circ_70006,RMVar_hsa_circ_351582,RMVar_hsa_circ_220659,RMVar_hsa_circ_301716 41293 RMVar_ID_41293 Human_SNP_ID_151280783 A-to-I Human chr3 - 122544651 122544651 122544651 ATTTTATTATTTTATTTAATTTTTTTTTTGGTAGAGACGGGGTTTCGCCATGTTGCCCAGACTGG ATTTTATTATTTTATTTAATTTTTTTTTTGGTGGAGACGGGGTTTCGCCATGTTGCCCAGACTGG T C PARP9 Ensembl:ENSG00000138496 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1178446308 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_220663,RMVar_hsa_circ_350069,RMVar_hsa_circ_360396,RMVar_hsa_circ_366531,RMVar_hsa_circ_354262 41294 RMVar_ID_41294 Human_SNP_ID_151280814 A-to-I Human chr3 - 122544784 122544784 122544784 TCACTCTGGTTGGAGTGCAGTGGCGTGATCTCAGCTCACTGCATCCTCTGCTTCACAGGCTCAAG TCACTCTGGTTGGAGTGCAGTGGCGTGATCTCCGCTCACTGCATCCTCTGCTTCACAGGCTCAAG T G PARP9 Ensembl:ENSG00000138496 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1228070730 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_220663,RMVar_hsa_circ_350069,RMVar_hsa_circ_360396,RMVar_hsa_circ_366531,RMVar_hsa_circ_354262 41295 RMVar_ID_41295 Human_SNP_ID_151280818 A-to-I Human chr3 - 122544814 122544814 122544814 CTTTTCTTTTTGAGACAAGTTCTGACTCTGTCACTCTGGTTGGAGTGCAGTGGCGTGATCTCAGC CTTTTCTTTTTGAGACAAGTTCTGACTCTGTCGCTCTGGTTGGAGTGCAGTGGCGTGATCTCAGC T C PARP9 Ensembl:ENSG00000138496 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1403981474 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_220663,RMVar_hsa_circ_350069,RMVar_hsa_circ_360396,RMVar_hsa_circ_366531,RMVar_hsa_circ_354262 41296 RMVar_ID_41296 Human_SNP_ID_151284028 A-to-I Human chr3 - 122557860 122557860 122557860 ATAAGGTAGTGTACCTGTTATCAATTGATGGTATGCCCCAGTTTAGTTGGCATTTTTTTCCCTTT ATAAGGTAGTGTACCTGTTATCAATTGATGGTGTGCCCCAGTTTAGTTGGCATTTTTTTCCCTTT T C PARP9 Ensembl:ENSG00000138496 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs188154270 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_366531,RMVar_hsa_circ_369116 41297 RMVar_ID_41297 Human_SNP_ID_151284029 A-to-I Human chr3 - 122557873 122557873 122557873 TAACAATACTGAAATAAGGTAGTGTACCTGTTATCAATTGATGGTATGCCCCAGTTTAGTTGGCA TAACAATACTGAAATAAGGTAGTGTACCTGTTGTCAATTGATGGTATGCCCCAGTTTAGTTGGCA T C PARP9 Ensembl:ENSG00000138496 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs899162191 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_366531,RMVar_hsa_circ_369116 41298 RMVar_ID_41298 Human_SNP_ID_151287617 A-to-I Human chr3 + 122570880 122570880 122570880 CCTGCCAGCTATAAAGTACTATGGAGTTATTTAAATTTTGCACCAAAGGACAGGGGGCTTTTGAA CCTGCCAGCTATAAAGTACTATGGAGTTATTTCAATTTTGCACCAAAGGACAGGGGGCTTTTGAA A C DTX3L Ensembl:ENSG00000163840 Protein coding intron GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-Seq:(High) rs1470639184 Functional Loss SNV dbSNP153 33..33 33 - - - 41299 RMVar_ID_41299 Human_SNP_ID_151287620 A-to-I Human chr3 + 122570897 122570897 122570897 ACTATGGAGTTATTTAAATTTTGCACCAAAGGACAGGGGGCTTTTGAATCCGAGATGAATACTAT ACTATGGAGTTATTTAAATTTTGCACCAAAGGCCAGGGGGCTTTTGAATCCGAGATGAATACTAT A C DTX3L Ensembl:ENSG00000163840 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1406321758 Functional Loss SNV dbSNP153 33..33 33 - - - 41300 RMVar_ID_41300 Human_SNP_ID_151287632 A-to-I Human chr3 + 122570932 122570932 122570932 GGGGGCTTTTGAATCCGAGATGAATACTATATAAGCTGATTTAATTTGAGGCGTTGTGTCTATCT GGGGGCTTTTGAATCCGAGATGAATACTATATGAGCTGATTTAATTTGAGGCGTTGTGTCTATCT A G DTX3L Ensembl:ENSG00000163840 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1422170658 Functional Loss SNV dbSNP153 33..33 33 - - - 41301 RMVar_ID_41301 Human_SNP_ID_151297467 A-to-I Human chr3 + 122612252 122612252 122612252 TAATTTTTGTGTTTTTGTAAAGATGGGGTTTCACCATGTTGCCCAGGCTGGTCTTGAACTCAAGG TAATTTTTGTGTTTTTGTAAAGATGGGGTTTCTCCATGTTGCCCAGGCTGGTCTTGAACTCAAGG A T PARP15 Ensembl:ENSG00000173200 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1246392341 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71462,RMVar_hsa_circ_356477,RMVar_hsa_circ_71978,RMVar_hsa_circ_362185,RMVar_hsa_circ_220667 41302 RMVar_ID_41302 Human_SNP_ID_151297904 A-to-I Human chr3 + 122613877 122613877 122613877 AGAGTCTCGTTCTGTTACCCAGGCTGGAGTGCAGTGGTGTGATCTCGGCTCACTGCAGCGGCGTG AGAGTCTCGTTCTGTTACCCAGGCTGGAGTGCCGTGGTGTGATCTCGGCTCACTGCAGCGGCGTG A C PARP15 Ensembl:ENSG00000173200 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs541408509 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71462,RMVar_hsa_circ_356477,RMVar_hsa_circ_362185,RMVar_hsa_circ_220667 41303 RMVar_ID_41303 Human_SNP_ID_151297925 A-to-I Human chr3 + 122613945 122613945 122613945 TCAGCTCAATGCAGCCTCCGCCTCCTGGGCTCAAGCAATCCTCCCATCTTAGCCTCCCTAGTAGC TCAGCTCAATGCAGCCTCCGCCTCCTGGGCTCGAGCAATCCTCCCATCTTAGCCTCCCTAGTAGC A G PARP15 Ensembl:ENSG00000173200 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs954610499 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71462,RMVar_hsa_circ_356477,RMVar_hsa_circ_362185,RMVar_hsa_circ_220667 41304 RMVar_ID_41304 Human_SNP_ID_151297948 A-to-I Human chr3 + 122614085 122614085 122614085 CCAGGCTGGTCCTGACCTCAGGTGATCCACCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGC CCAGGCTGGTCCTGACCTCAGGTGATCCACCCCCCTCAGCCTCCCAAAGTGCTGGGATTACAGGC A C PARP15 Ensembl:ENSG00000173200 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs974163075 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71462,RMVar_hsa_circ_356477,RMVar_hsa_circ_362185,RMVar_hsa_circ_220667 41305 RMVar_ID_41305 Human_SNP_ID_151297949 A-to-I Human chr3 + 122614085 122614085 122614085 CCAGGCTGGTCCTGACCTCAGGTGATCCACCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGC CCAGGCTGGTCCTGACCTCAGGTGATCCACCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGC A G PARP15 Ensembl:ENSG00000173200 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs974163075 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71462,RMVar_hsa_circ_356477,RMVar_hsa_circ_362185,RMVar_hsa_circ_220667 41306 RMVar_ID_41306 Human_SNP_ID_151298088 A-to-I Human chr3 + 122614771 122614771 122614771 AGAAACATGGACTGGTGCAGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCTGAGGCAGGG AGAAACATGGACTGGTGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGG A G PARP15 Ensembl:ENSG00000173200 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs995554663 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71462,RMVar_hsa_circ_356477,RMVar_hsa_circ_362185,RMVar_hsa_circ_220667 41307 RMVar_ID_41307 Human_SNP_ID_151298089 A-to-I Human chr3 + 122614771 122614771 122614771 AGAAACATGGACTGGTGCAGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCTGAGGCAGGG AGAAACATGGACTGGTGCAGTGGCTCACGCCTTTAATCCCAGCACTTTGGGAGGCTGAGGCAGGG A T PARP15 Ensembl:ENSG00000173200 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs995554663 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71462,RMVar_hsa_circ_356477,RMVar_hsa_circ_362185,RMVar_hsa_circ_220667 41308 RMVar_ID_41308 Human_SNP_ID_151298148 A-to-I Human chr3 + 122615009 122615009 122615009 TCAAGATCATGCCACTGCACTCCAGCCTGGGCAACAGAATGAGACTCTGTCTGCAAAAAAAAAAA TCAAGATCATGCCACTGCACTCCAGCCTGGGCGACAGAATGAGACTCTGTCTGCAAAAAAAAAAA A G PARP15 Ensembl:ENSG00000173200 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs978461352 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71462,RMVar_hsa_circ_356477,RMVar_hsa_circ_362185,RMVar_hsa_circ_220667 41309 RMVar_ID_41309 Human_SNP_ID_151329199 A-to-I Human chr3 - 122740786 122740786 122740786 TTTTTTGATCGCTGCAGAACATCTGAGGTAGTAGAAATCCAAGCACTGAGAACAGATGGAGAGCA TTTTTTGATCGCTGCAGAACATCTGAGGTAGTGGAAATCCAAGCACTGAGAACAGATGGAGAGCA T C HSPBAP1 Ensembl:ENSG00000169087 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs148099222 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14590224 Human_Splice_Rec_473960,Human_Splice_Rec_473962 Human_miRNA_ID_2377542,Human_miRNA_ID_2842699,Human_miRNA_ID_3092617 RMVar_hsa_circ_102435,RMVar_hsa_circ_220674,RMVar_hsa_circ_220673,RMVar_hsa_circ_220675 41310 RMVar_ID_41310 Human_SNP_ID_151428044 A-to-I Human chr3 + 123148339 123148339 123148339 GCTGTAATCCTAGCACTTTGGGAAGTAGAGGCAGGAGGATCTCTTGAGTTCAGGAGTTCAAGACC GCTGTAATCCTAGCACTTTGGGAAGTAGAGGCGGGAGGATCTCTTGAGTTCAGGAGTTCAAGACC A G PDIA5 Ensembl:ENSG00000065485 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474482472 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_220694,RMVar_hsa_circ_369588,RMVar_hsa_circ_126757,RMVar_hsa_circ_220695,RMVar_hsa_circ_95782,RMVar_hsa_circ_220707,RMVar_hsa_circ_372297,RMVar_hsa_circ_29142,RMVar_hsa_circ_25017,RMVar_hsa_circ_220713,RMVar_hsa_circ_75858,RMVar_hsa_circ_14444,RMVar_hsa_circ_358605,RMVar_hsa_circ_220718,RMVar_hsa_circ_357534 41311 RMVar_ID_41311 Human_SNP_ID_151428073 A-to-I Human chr3 + 123148446 123148446 123148446 AAAAAATTACCTGGGCATGGTGGTGTGCGCCTATAGTCCCAGCACTTTGGGAATCTGAGGTGGGA AAAAAATTACCTGGGCATGGTGGTGTGCGCCTGTAGTCCCAGCACTTTGGGAATCTGAGGTGGGA A G PDIA5 Ensembl:ENSG00000065485 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1010413145 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_220694,RMVar_hsa_circ_369588,RMVar_hsa_circ_126757,RMVar_hsa_circ_220695,RMVar_hsa_circ_95782,RMVar_hsa_circ_220707,RMVar_hsa_circ_372297,RMVar_hsa_circ_29142,RMVar_hsa_circ_25017,RMVar_hsa_circ_220713,RMVar_hsa_circ_75858,RMVar_hsa_circ_14444,RMVar_hsa_circ_358605,RMVar_hsa_circ_220718,RMVar_hsa_circ_357534 41312 RMVar_ID_41312 Human_SNP_ID_151428082 A-to-I Human chr3 + 123148489 123148489 123148489 ACTTTGGGAATCTGAGGTGGGAGGATTGCTTGAAGCCGGGAGGTTGAGGCTACAGTGAGCTGGGA ACTTTGGGAATCTGAGGTGGGAGGATTGCTTGGAGCCGGGAGGTTGAGGCTACAGTGAGCTGGGA A G PDIA5 Ensembl:ENSG00000065485 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1356594913 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_220694,RMVar_hsa_circ_369588,RMVar_hsa_circ_126757,RMVar_hsa_circ_220695,RMVar_hsa_circ_95782,RMVar_hsa_circ_220707,RMVar_hsa_circ_372297,RMVar_hsa_circ_29142,RMVar_hsa_circ_25017,RMVar_hsa_circ_220713,RMVar_hsa_circ_75858,RMVar_hsa_circ_14444,RMVar_hsa_circ_358605,RMVar_hsa_circ_220718,RMVar_hsa_circ_357534 41313 RMVar_ID_41313 Human_SNP_ID_151442030 A-to-I Human chr3 + 123206233 123206233 123206233 GGGCCTGCTTCAGCCTCCCCAAAGCAAGTACTATAGGCGTGTGCCACCATGCCCAGCTGATTTTT GGGCCTGCTTCAGCCTCCCCAAAGCAAGTACTGTAGGCGTGTGCCACCATGCCCAGCTGATTTTT A G PDIA5,SEC22A Ensembl:ENSG00000065485,Ensembl:ENSG00000121542 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs369114788 Functional Loss SNV dbSNP153 33..33 33 - - - 41314 RMVar_ID_41314 Human_SNP_ID_151442048 A-to-I Human chr3 + 123206284 123206283 123206285 CCCAGCTGATTTTTAATTTTTTTTATAGAGACAGAGCCTCACCATGTTTCTAGGTTGGTCTTGAA CCCAGCTGATTTTTAATTTTTTTTATAGAGAC__AGCCTCACCATGTTTCTAGGTTGGTCTTGAA CAG C PDIA5,SEC22A Ensembl:ENSG00000065485,Ensembl:ENSG00000121542 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1341364653 Functional Loss DEL dbSNP153 33..34 33 - - - 41315 RMVar_ID_41315 Human_SNP_ID_151442165 A-to-I Human chr3 + 123206819 123206819 123206819 CTCTTTAAATGAATGGAGAGGCTGGGCGTGGTAGCTCATGCCTGTAATCCTAGTACTTTGGGAGG CTCTTTAAATGAATGGAGAGGCTGGGCGTGGTCGCTCATGCCTGTAATCCTAGTACTTTGGGAGG A C PDIA5,SEC22A Ensembl:ENSG00000065485,Ensembl:ENSG00000121542 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs576055745 Functional Loss SNV dbSNP153 33..33 33 - - - 41316 RMVar_ID_41316 Human_SNP_ID_151442655 A-to-I Human chr3 + 123208826 123208826 123208826 TTGTTTTTTTTTTCCTCCTGAGACGGAGTCTCACTCTGTCGCCCAGGCTGGAGCTCAGTGACGCG TTGTTTTTTTTTTCCTCCTGAGACGGAGTCTCTCTCTGTCGCCCAGGCTGGAGCTCAGTGACGCG A T PDIA5,SEC22A Ensembl:ENSG00000065485,Ensembl:ENSG00000121542 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs954845974 Functional Loss SNV dbSNP153 33..33 33 - - - 41317 RMVar_ID_41317 Human_SNP_ID_151448834 A-to-I Human chr3 + 123235128 123235125 123235129 TTGCCCAGGCTGGTCTCGCACTCGTCGGCTCAAACAATCCTCCCACCTCAGGCTCTAGAGTAGTC TTGCCCAGGCTGGTCTCGCACTCGTCGGCT____CAATCCTCCCACCTCAGGCTCTAGAGTAGTC TCAAA T SEC22A Ensembl:ENSG00000121542 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1304503574 Functional Loss DEL dbSNP153 31..34 33 - - - RMVar_hsa_circ_220722,RMVar_hsa_circ_270159,RMVar_hsa_circ_295770,RMVar_hsa_circ_220720,RMVar_hsa_circ_220721,RMVar_hsa_circ_264864,RMVar_hsa_circ_272249,RMVar_hsa_circ_301558,RMVar_hsa_circ_220727,RMVar_hsa_circ_220728,RMVar_hsa_circ_220729,RMVar_hsa_circ_292477 41318 RMVar_ID_41318 Human_SNP_ID_151449505 A-to-I Human chr3 + 123238039 123238039 123238039 AGCTAGACATGGTGGCACGTGACTGTAGTCCCAGCTACTAGAAAGGCTGAGGCAGGAGGATTGCT AGCTAGACATGGTGGCACGTGACTGTAGTCCCGGCTACTAGAAAGGCTGAGGCAGGAGGATTGCT A G SEC22A Ensembl:ENSG00000121542 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1305101767 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_220722,RMVar_hsa_circ_270159,RMVar_hsa_circ_295770,RMVar_hsa_circ_220720,RMVar_hsa_circ_220721,RMVar_hsa_circ_264864,RMVar_hsa_circ_272249,RMVar_hsa_circ_301558,RMVar_hsa_circ_220727,RMVar_hsa_circ_220728,RMVar_hsa_circ_220729,RMVar_hsa_circ_292477 41319 RMVar_ID_41319 Human_SNP_ID_151513776 A-to-I Human chr3 - 123494369 123494369 123494369 GTTCTCTGGAATGCTCTGAAGTTATGGCTGGGACCTATCCCCTCACATCTAATGAATGAATTATA GTTCTCTGGAATGCTCTGAAGTTATGGCTGGGGCCTATCCCCTCACATCTAATGAATGAATTATA T C HACD2 Ensembl:ENSG00000206527 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1386713734 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_587612,Human_RBP_ID_8210265,Human_RBP_ID_14592222,Human_RBP_ID_17992730,Human_RBP_ID_22397268,Human_RBP_ID_23964910,Human_RBP_ID_27497214 41320 RMVar_ID_41320 Human_SNP_ID_151535791 A-to-I Human chr3 + 123588618 123588618 123588618 AAAATTAGCTGGGTGTGGTGGTGCGCGCCTGTAGTCCCAGCTACTTGGGAGACTGAGGCAAGAGA AAAATTAGCTGGGTGTGGTGGTGCGCGCCTGTGGTCCCAGCTACTTGGGAGACTGAGGCAAGAGA A G MYLK-AS1 Ensembl:ENSG00000239523 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs961056222 Functional Loss SNV dbSNP153 33..33 33 - - - 41321 RMVar_ID_41321 Human_SNP_ID_151535985 A-to-I Human chr3 + 123589370 123589370 123589370 CACCTGCCTCGGCCTCCCAAAATGCTGGGATTATAGGCATGAACCACCACACCCGACCTTCCTGA CACCTGCCTCGGCCTCCCAAAATGCTGGGATTGTAGGCATGAACCACCACACCCGACCTTCCTGA A G MYLK-AS1 Ensembl:ENSG00000239523 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1050702361 Functional Loss SNV dbSNP153 33..33 33 - - - 41322 RMVar_ID_41322 Human_SNP_ID_151539523 A-to-I Human chr3 + 123605718 123605718 123605718 CCCTCTTCAGCCTCCCAAGAAGCTGGGACTACAGACACATACCATGACACCCGGCTAATTAAAAC CCCTCTTCAGCCTCCCAAGAAGCTGGGACTACGGACACATACCATGACACCCGGCTAATTAAAAC A G MYLK-AS1 Ensembl:ENSG00000239523 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1205410887 Functional Loss SNV dbSNP153 33..33 33 - - - 41323 RMVar_ID_41323 Human_SNP_ID_151611647 A-to-I Human chr3 - 123917038 123917038 123917038 GAGATCGAGACCATCCCGGCTAACACAGTGAAACCCCGTCGCTACTAAAAAATACAGAAAAATTA GAGATCGAGACCATCCCGGCTAACACAGTGAAGCCCCGTCGCTACTAAAAAATACAGAAAAATTA T C CCDC14 Ensembl:ENSG00000175455 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs961007349 Functional Loss SNV dbSNP153 33..33 33 - - - 41324 RMVar_ID_41324 Human_SNP_ID_151611648 A-to-I Human chr3 - 123917038 123917038 123917038 GAGATCGAGACCATCCCGGCTAACACAGTGAAACCCCGTCGCTACTAAAAAATACAGAAAAATTA GAGATCGAGACCATCCCGGCTAACACAGTGAACCCCCGTCGCTACTAAAAAATACAGAAAAATTA T G CCDC14 Ensembl:ENSG00000175455 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs961007349 Functional Loss SNV dbSNP153 33..33 33 - - - 41325 RMVar_ID_41325 Human_SNP_ID_151611652 A-to-I Human chr3 - 123917044 123917043 123917045 GGTCAGGAGATCGAGACCATCCCGGCTAACACAGTGAAACCCCGTCGCTACTAAAAAATACAGAA GGTCAGGAGATCGAGACCATCCCGGCTAACA__GTGAAACCCCGTCGCTACTAAAAAATACAGAA CTG C CCDC14 Ensembl:ENSG00000175455 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1416529620 Functional Loss DEL dbSNP153 32..33 33 - - - 41326 RMVar_ID_41326 Human_SNP_ID_151611653 A-to-I Human chr3 - 123917044 123917044 123917044 GGTCAGGAGATCGAGACCATCCCGGCTAACACAGTGAAACCCCGTCGCTACTAAAAAATACAGAA GGTCAGGAGATCGAGACCATCCCGGCTAACACGGTGAAACCCCGTCGCTACTAAAAAATACAGAA T C CCDC14 Ensembl:ENSG00000175455 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1469543234 Functional Loss SNV dbSNP153 33..33 33 - - - 41327 RMVar_ID_41327 Human_SNP_ID_151614546 A-to-I Human chr3 - 123929567 123929567 123929567 TGGTTGCAGGGCCTCATGCCTGTAACCCCAGCACTTTGGGAGGCCGAGGTGGGTGGATCGCCTGG TGGTTGCAGGGCCTCATGCCTGTAACCCCAGCCCTTTGGGAGGCCGAGGTGGGTGGATCGCCTGG T G CCDC14 Ensembl:ENSG00000175455 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1015303686 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25692427 41328 RMVar_ID_41328 Human_SNP_ID_151722031 A-to-I Human chr3 + 124401318 124401318 124401318 CTTGAACTCAGGAGCTCAAGACCAGCCTGGGCAACGTGGTGAAACTCCATCTCCACCAAAAATAT CTTGAACTCAGGAGCTCAAGACCAGCCTGGGCTACGTGGTGAAACTCCATCTCCACCAAAAATAT A T KALRN Ensembl:ENSG00000160145 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs911758294 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33119,RMVar_hsa_circ_43550,RMVar_hsa_circ_320722,RMVar_hsa_circ_378395,RMVar_hsa_circ_302640,RMVar_hsa_circ_15830,RMVar_hsa_circ_43384,RMVar_hsa_circ_220788,RMVar_hsa_circ_220789,RMVar_hsa_circ_220790,RMVar_hsa_circ_328177,RMVar_hsa_circ_378149,RMVar_hsa_circ_220791,RMVar_hsa_circ_342025,RMVar_hsa_circ_45695,RMVar_hsa_circ_220793,RMVar_hsa_circ_5669,RMVar_hsa_circ_220792 41329 RMVar_ID_41329 Human_SNP_ID_151797660 A-to-I Human chr3 - 124725984 124725984 124725984 TTCTGCACCTTGAAAATATAGAGCTATTTATCAATACTGTGGAGTGATTTTAAATCAATTGTTAC TTCTGCACCTTGAAAATATAGAGCTATTTATCGATACTGTGGAGTGATTTTAAATCAATTGTTAC T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs997142609 Functional Loss SNV dbSNP153 33..33 33 - - - 41330 RMVar_ID_41330 Human_SNP_ID_151863060 A-to-I Human chr3 - 124987148 124987148 124987148 CAGGCTGGAGTGCAGTGGCCTGATCATGGCTCACTGTAGCCTCAACCTCTCAGGCTCAAGCAATC CAGGCTGGAGTGCAGTGGCCTGATCATGGCTCCCTGTAGCCTCAACCTCTCAGGCTCAAGCAATC T G HEG1 Ensembl:ENSG00000173706 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1405547014 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8589,RMVar_hsa_circ_87104,RMVar_hsa_circ_265500,RMVar_hsa_circ_220847,RMVar_hsa_circ_269564,RMVar_hsa_circ_220849 41331 RMVar_ID_41331 Human_SNP_ID_151865078 A-to-I Human chr3 - 124995199 124995199 124995199 GACCTCCTGGGCTCAAGTGATCCTCCCACCTCAGCCTCCCAAGTAGCTGGGACTACAGGTCCTTG GACCTCCTGGGCTCAAGTGATCCTCCCACCTCGGCCTCCCAAGTAGCTGGGACTACAGGTCCTTG T C HEG1 Ensembl:ENSG00000173706 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs977668808 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8589,RMVar_hsa_circ_87104,RMVar_hsa_circ_265500,RMVar_hsa_circ_220847,RMVar_hsa_circ_269564,RMVar_hsa_circ_220849,RMVar_hsa_circ_220850,RMVar_hsa_circ_97608,RMVar_hsa_circ_328139 41332 RMVar_ID_41332 Human_SNP_ID_151885714 A-to-I Human chr3 - 125083635 125083635 125083635 TCACTGCAACCTCTGCTTCCCGAGTTCAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGA TCACTGCAACCTCTGCTTCCCGAGTTCAAGCACTTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGA T G SLC12A8 Ensembl:ENSG00000221955 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1560045224 Functional Loss SNV dbSNP153 33..33 33 - - - 41333 RMVar_ID_41333 Human_SNP_ID_151885716 A-to-I Human chr3 - 125083645 125083645 125083645 CAATCTTGGCTCACTGCAACCTCTGCTTCCCGAGTTCAAGCAATTCTCCTGCCTCAGCCTCCTGA CAATCTTGGCTCACTGCAACCTCTGCTTCCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTGA T C SLC12A8 Ensembl:ENSG00000221955 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1199701356 Functional Loss SNV dbSNP153 33..33 33 - - - 41334 RMVar_ID_41334 Human_SNP_ID_151894150 A-to-I Human chr3 - 125118840 125118834 125118840 CTCTTGGGTTTTGCAGGTGGTTTCTGTACATCATCTTCGTCTTCCTCCTGGGCGCCATCTGCACT CTCTTGGGTTTTGCAGGTGGTTTCTGTACATC______GTCTTCCTCCTGGGCGCCATCTGCACT CGAAGAT C SLC12A8 Ensembl:ENSG00000221955 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1392435681 Functional Loss DEL dbSNP153 33..38 33 - - - Human_Splice_Rec_476614,Human_Splice_Rec_476615,Human_Splice_Rec_476638,Human_Splice_Rec_476639,Human_Splice_Rec_476662,Human_Splice_Rec_476663,Human_Splice_Rec_476678,Human_Splice_Rec_476679,Human_Splice_Rec_476698,Human_Splice_Rec_476699,Human_Splice_Rec_476714,Human_Splice_Rec_476715,Human_Splice_Rec_476730,Human_Splice_Rec_476731,Human_Splice_Rec_476749,Human_Splice_Rec_476758,Human_Splice_Rec_476759,Human_Splice_Rec_476768,Human_Splice_Rec_476769,Human_Splice_Rec_476786,Human_Splice_Rec_476787 RMVar_hsa_circ_79250,RMVar_hsa_circ_83609,RMVar_hsa_circ_220857,RMVar_hsa_circ_220858,RMVar_hsa_circ_295023,RMVar_hsa_circ_220860,RMVar_hsa_circ_296013,RMVar_hsa_circ_322494 41335 RMVar_ID_41335 Human_SNP_ID_151894153 A-to-I Human chr3 - 125118840 125118840 125118840 CTCTTGGGTTTTGCAGGTGGTTTCTGTACATCATCTTCGTCTTCCTCCTGGGCGCCATCTGCACT CTCTTGGGTTTTGCAGGTGGTTTCTGTACATCGTCTTCGTCTTCCTCCTGGGCGCCATCTGCACT T C SLC12A8 Ensembl:ENSG00000221955 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs621383 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_Splice_Rec_476614,Human_Splice_Rec_476615,Human_Splice_Rec_476638,Human_Splice_Rec_476639,Human_Splice_Rec_476662,Human_Splice_Rec_476663,Human_Splice_Rec_476678,Human_Splice_Rec_476679,Human_Splice_Rec_476698,Human_Splice_Rec_476699,Human_Splice_Rec_476714,Human_Splice_Rec_476715,Human_Splice_Rec_476730,Human_Splice_Rec_476731,Human_Splice_Rec_476749,Human_Splice_Rec_476758,Human_Splice_Rec_476759,Human_Splice_Rec_476768,Human_Splice_Rec_476769,Human_Splice_Rec_476786,Human_Splice_Rec_476787 RMVar_hsa_circ_79250,RMVar_hsa_circ_83609,RMVar_hsa_circ_220857,RMVar_hsa_circ_220858,RMVar_hsa_circ_295023,RMVar_hsa_circ_220860,RMVar_hsa_circ_296013,RMVar_hsa_circ_322494 41336 RMVar_ID_41336 Human_SNP_ID_151923755 A-to-I Human chr3 - 125240553 125240553 125240553 CACTGTGTCACCCAGACTGGTCCTGAACTTCTAGACTCAAGTGATCCTCCCGCCTGAACCTCTCG CACTGTGTCACCCAGACTGGTCCTGAACTTCTGGACTCAAGTGATCCTCCCGCCTGAACCTCTCG T C ZNF148 Ensembl:ENSG00000163848 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs576167524 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14596660 RMVar_hsa_circ_79250,RMVar_hsa_circ_220857,RMVar_hsa_circ_76236,RMVar_hsa_circ_220861,RMVar_hsa_circ_220864,RMVar_hsa_circ_83757,RMVar_hsa_circ_265142 41337 RMVar_ID_41337 Human_SNP_ID_151929363 A-to-I Human chr3 - 125263469 125263469 125263469 TTGGCTCACTGCAACCTCAGTCTCCCGGGTTCAAGTGATTCTCCTGCCCCAGCCTCCTGAGTACC TTGGCTCACTGCAACCTCAGTCTCCCGGGTTCGAGTGATTCTCCTGCCCCAGCCTCCTGAGTACC T C ZNF148 Ensembl:ENSG00000163848 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs927937663 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25693155 RMVar_hsa_circ_79250,RMVar_hsa_circ_220857,RMVar_hsa_circ_76236,RMVar_hsa_circ_220861,RMVar_hsa_circ_220864,RMVar_hsa_circ_83757,RMVar_hsa_circ_265142 41338 RMVar_ID_41338 Human_SNP_ID_151949996 A-to-I Human chr3 - 125349803 125349803 125349803 AGGGTCTGGCTCTGTCATCTGAGCTGTAGTGCAGTGGTGAGATCATAGCTCACTGCAACCTCAAA AGGGTCTGGCTCTGTCATCTGAGCTGTAGTGCCGTGGTGAGATCATAGCTCACTGCAACCTCAAA T G ZNF148 Ensembl:ENSG00000163848 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924414741 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14598875 RMVar_hsa_circ_220890 41339 RMVar_ID_41339 Human_SNP_ID_151951013 A-to-I Human chr3 - 125353728 125353728 125353728 ATTCTGGGCTGTGCACAGTGGCTCATGCCTGTAATCCCTACACTATGGGAGACCAAGGCAGGTGA ATTCTGGGCTGTGCACAGTGGCTCATGCCTGTGATCCCTACACTATGGGAGACCAAGGCAGGTGA T C ZNF148 Ensembl:ENSG00000163848 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1183931666 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17573825 RMVar_hsa_circ_220890 41340 RMVar_ID_41340 Human_SNP_ID_151951040 A-to-I Human chr3 - 125353817 125353817 125353817 TTCCCGCTTTGGCTTCCCAAAGTGCTGGGATTACAAGCATGAACCACTGAACCTGGCCTCACATG TTCCCGCTTTGGCTTCCCAAAGTGCTGGGATTGCAAGCATGAACCACTGAACCTGGCCTCACATG T C ZNF148 Ensembl:ENSG00000163848 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs374319144 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7115015 RMVar_hsa_circ_220890 41341 RMVar_ID_41341 Human_SNP_ID_151951053 A-to-I Human chr3 - 125353882 125353882 125353882 CTATATAGAGATGGGGTCTTGCTATGTTGCCCAGGCTGGTCTCAAACTCCTAGGCTCACGTGATC CTATATAGAGATGGGGTCTTGCTATGTTGCCCGGGCTGGTCTCAAACTCCTAGGCTCACGTGATC T C ZNF148 Ensembl:ENSG00000163848 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965564394 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_220890 41342 RMVar_ID_41342 Human_SNP_ID_151953471 A-to-I Human chr3 - 125364207 125364207 125364207 TTTAGTAGAGACAGGGTTTTGCCATATTGGCCAGGCTTTTCTCAAACTCCTCACCTCAAGTGATC TTTAGTAGAGACAGGGTTTTGCCATATTGGCCCGGCTTTTCTCAAACTCCTCACCTCAAGTGATC T G ZNF148 Ensembl:ENSG00000163848 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,temporal_cortex - 29129909,30559470 RNA-Seq:(High) rs926942974 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_220890 41343 RMVar_ID_41343 Human_SNP_ID_151975247 A-to-I Human chr3 - 125455849 125455849 125455849 CCACGCCCGACCAATTTTTTTTTTGCACTTTTAGTACAGACGGGGTTTCACCATGTTAGCCAAGA CCACGCCCGACCAATTTTTTTTTTGCACTTTTCGTACAGACGGGGTTTCACCATGTTAGCCAAGA T G SNX4 Ensembl:ENSG00000114520 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1279593278 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_220892,RMVar_hsa_circ_266705,RMVar_hsa_circ_301967,RMVar_hsa_circ_330096,RMVar_hsa_circ_291377,RMVar_hsa_circ_91232,RMVar_hsa_circ_220893,RMVar_hsa_circ_8244,RMVar_hsa_circ_38805,RMVar_hsa_circ_220895,RMVar_hsa_circ_220894,RMVar_hsa_circ_220898,RMVar_hsa_circ_105641,RMVar_hsa_circ_326711,RMVar_hsa_circ_360162,RMVar_hsa_circ_282808,RMVar_hsa_circ_220899,RMVar_hsa_circ_220897 41344 RMVar_ID_41344 Human_SNP_ID_151975346 A-to-I Human chr3 - 125456410 125456410 125456410 GTGATCCTCCCACCTCCGCCTCCCAAAGTGCTAGGATTACAGGGGTAAGCCACCATGCCTAGTCT GTGATCCTCCCACCTCCGCCTCCCAAAGTGCTGGGATTACAGGGGTAAGCCACCATGCCTAGTCT T C SNX4 Ensembl:ENSG00000114520 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs534755378 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_220892,RMVar_hsa_circ_266705,RMVar_hsa_circ_301967,RMVar_hsa_circ_330096,RMVar_hsa_circ_291377,RMVar_hsa_circ_91232,RMVar_hsa_circ_220893,RMVar_hsa_circ_8244,RMVar_hsa_circ_38805,RMVar_hsa_circ_220895,RMVar_hsa_circ_220894,RMVar_hsa_circ_220898,RMVar_hsa_circ_105641,RMVar_hsa_circ_326711,RMVar_hsa_circ_360162,RMVar_hsa_circ_282808,RMVar_hsa_circ_220899,RMVar_hsa_circ_220897 41345 RMVar_ID_41345 Human_SNP_ID_151975356 A-to-I Human chr3 - 125456443 125456443 125456443 TTGACCAGGGTGGTCTCAAACTCCTGGACTCAAGTGATCCTCCCACCTCCGCCTCCCAAAGTGCT TTGACCAGGGTGGTCTCAAACTCCTGGACTCACGTGATCCTCCCACCTCCGCCTCCCAAAGTGCT T G SNX4 Ensembl:ENSG00000114520 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1249247115 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_220892,RMVar_hsa_circ_266705,RMVar_hsa_circ_301967,RMVar_hsa_circ_330096,RMVar_hsa_circ_291377,RMVar_hsa_circ_91232,RMVar_hsa_circ_220893,RMVar_hsa_circ_8244,RMVar_hsa_circ_38805,RMVar_hsa_circ_220895,RMVar_hsa_circ_220894,RMVar_hsa_circ_220898,RMVar_hsa_circ_105641,RMVar_hsa_circ_326711,RMVar_hsa_circ_360162,RMVar_hsa_circ_282808,RMVar_hsa_circ_220899,RMVar_hsa_circ_220897 41346 RMVar_ID_41346 Human_SNP_ID_151975370 A-to-I Human chr3 - 125456519 125456519 125456519 CCTCAGCCTCTTGAGTAGTTGGGACCACAGGCATGTGCCCCCATGCCTGGCTAATTTTGTTTATA CCTCAGCCTCTTGAGTAGTTGGGACCACAGGCGTGTGCCCCCATGCCTGGCTAATTTTGTTTATA T C SNX4 Ensembl:ENSG00000114520 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1256746570 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_220892,RMVar_hsa_circ_266705,RMVar_hsa_circ_301967,RMVar_hsa_circ_330096,RMVar_hsa_circ_291377,RMVar_hsa_circ_91232,RMVar_hsa_circ_220893,RMVar_hsa_circ_8244,RMVar_hsa_circ_38805,RMVar_hsa_circ_220895,RMVar_hsa_circ_220894,RMVar_hsa_circ_220898,RMVar_hsa_circ_105641,RMVar_hsa_circ_326711,RMVar_hsa_circ_360162,RMVar_hsa_circ_282808,RMVar_hsa_circ_220899,RMVar_hsa_circ_220897 41347 RMVar_ID_41347 Human_SNP_ID_151975371 A-to-I Human chr3 - 125456519 125456519 125456519 CCTCAGCCTCTTGAGTAGTTGGGACCACAGGCATGTGCCCCCATGCCTGGCTAATTTTGTTTATA CCTCAGCCTCTTGAGTAGTTGGGACCACAGGCCTGTGCCCCCATGCCTGGCTAATTTTGTTTATA T G SNX4 Ensembl:ENSG00000114520 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1256746570 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_220892,RMVar_hsa_circ_266705,RMVar_hsa_circ_301967,RMVar_hsa_circ_330096,RMVar_hsa_circ_291377,RMVar_hsa_circ_91232,RMVar_hsa_circ_220893,RMVar_hsa_circ_8244,RMVar_hsa_circ_38805,RMVar_hsa_circ_220895,RMVar_hsa_circ_220894,RMVar_hsa_circ_220898,RMVar_hsa_circ_105641,RMVar_hsa_circ_326711,RMVar_hsa_circ_360162,RMVar_hsa_circ_282808,RMVar_hsa_circ_220899,RMVar_hsa_circ_220897 41348 RMVar_ID_41348 Human_SNP_ID_151975721 A-to-I Human chr3 - 125457716 125457716 125457716 AAAATTAGCTGGGTGTGGTGGCGCATGCCTGTAATCCCATCTACTAGGGAAGCTGAGGCAGGAGA AAAATTAGCTGGGTGTGGTGGCGCATGCCTGTGATCCCATCTACTAGGGAAGCTGAGGCAGGAGA T C SNX4 Ensembl:ENSG00000114520 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1342943781 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_153777 RMVar_hsa_circ_3042,RMVar_hsa_circ_220892,RMVar_hsa_circ_266705,RMVar_hsa_circ_301967,RMVar_hsa_circ_330096,RMVar_hsa_circ_91232,RMVar_hsa_circ_220893,RMVar_hsa_circ_8244,RMVar_hsa_circ_38805,RMVar_hsa_circ_220894,RMVar_hsa_circ_220898,RMVar_hsa_circ_105641,RMVar_hsa_circ_360162,RMVar_hsa_circ_282808,RMVar_hsa_circ_220899,RMVar_hsa_circ_41436,RMVar_hsa_circ_303263,RMVar_hsa_circ_13062,RMVar_hsa_circ_220900 41349 RMVar_ID_41349 Human_SNP_ID_151976269 A-to-I Human chr3 - 125459597 125459597 125459597 CCGTCTCTACTAAAATTACAAAAAAGTTAGCCAGGCATAGTGGTGGGTGCCTGTAATCCCAGCTG CCGTCTCTACTAAAATTACAAAAAAGTTAGCCGGGCATAGTGGTGGGTGCCTGTAATCCCAGCTG T C SNX4 Ensembl:ENSG00000114520 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1305981036 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3042,RMVar_hsa_circ_220892,RMVar_hsa_circ_266705,RMVar_hsa_circ_301967,RMVar_hsa_circ_330096,RMVar_hsa_circ_91232,RMVar_hsa_circ_220893,RMVar_hsa_circ_8244,RMVar_hsa_circ_38805,RMVar_hsa_circ_220894,RMVar_hsa_circ_220898,RMVar_hsa_circ_105641,RMVar_hsa_circ_360162,RMVar_hsa_circ_282808,RMVar_hsa_circ_220899,RMVar_hsa_circ_41436,RMVar_hsa_circ_303263,RMVar_hsa_circ_13062,RMVar_hsa_circ_220900 41350 RMVar_ID_41350 Human_SNP_ID_151976375 A-to-I Human chr3 - 125460037 125460037 125460037 GGCGCCCGCCAACACACCCAGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCGTTGTTG GGCGCCCGCCAACACACCCAGCTAATTTTTGTGTTTTTAGTAGAGACAGGGTTTCACCGTTGTTG T C SNX4 Ensembl:ENSG00000114520 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs969571087 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3042,RMVar_hsa_circ_220892,RMVar_hsa_circ_266705,RMVar_hsa_circ_301967,RMVar_hsa_circ_330096,RMVar_hsa_circ_91232,RMVar_hsa_circ_220893,RMVar_hsa_circ_8244,RMVar_hsa_circ_38805,RMVar_hsa_circ_220894,RMVar_hsa_circ_220898,RMVar_hsa_circ_105641,RMVar_hsa_circ_360162,RMVar_hsa_circ_282808,RMVar_hsa_circ_220899,RMVar_hsa_circ_41436,RMVar_hsa_circ_303263,RMVar_hsa_circ_13062,RMVar_hsa_circ_220900 41351 RMVar_ID_41351 Human_SNP_ID_151976971 A-to-I Human chr3 - 125462407 125462407 125462407 TTTTGTATTTTTTGTAGAGACAGGGTCTTGCCATGTTGCCCAGGCTGGTCTCGAACTCCTGGGTT TTTTGTATTTTTTGTAGAGACAGGGTCTTGCCGTGTTGCCCAGGCTGGTCTCGAACTCCTGGGTT T C SNX4 Ensembl:ENSG00000114520 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1406182725 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3042,RMVar_hsa_circ_266705,RMVar_hsa_circ_330096,RMVar_hsa_circ_91232,RMVar_hsa_circ_220893,RMVar_hsa_circ_8244,RMVar_hsa_circ_38805,RMVar_hsa_circ_105641,RMVar_hsa_circ_360162,RMVar_hsa_circ_220899,RMVar_hsa_circ_41436,RMVar_hsa_circ_13062,RMVar_hsa_circ_56237,RMVar_hsa_circ_344814,RMVar_hsa_circ_220900,RMVar_hsa_circ_71103,RMVar_hsa_circ_220901 41352 RMVar_ID_41352 Human_SNP_ID_151976978 A-to-I Human chr3 - 125462441 125462441 125462441 GGACTATAGGCATGCACTACCATGTCCAGCTAATTTTTGTATTTTTTGTAGAGACAGGGTCTTGC GGACTATAGGCATGCACTACCATGTCCAGCTATTTTTTGTATTTTTTGTAGAGACAGGGTCTTGC T A SNX4 Ensembl:ENSG00000114520 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs925559333 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3042,RMVar_hsa_circ_266705,RMVar_hsa_circ_330096,RMVar_hsa_circ_91232,RMVar_hsa_circ_220893,RMVar_hsa_circ_8244,RMVar_hsa_circ_38805,RMVar_hsa_circ_105641,RMVar_hsa_circ_360162,RMVar_hsa_circ_220899,RMVar_hsa_circ_41436,RMVar_hsa_circ_13062,RMVar_hsa_circ_56237,RMVar_hsa_circ_344814,RMVar_hsa_circ_220900,RMVar_hsa_circ_71103,RMVar_hsa_circ_220901 41353 RMVar_ID_41353 Human_SNP_ID_151977380 A-to-I Human chr3 - 125463986 125463986 125463986 CCAGGCTGGTCTCAAACTCCTGGGCTCAAGTAATCCACCGTCATAGCCTCTCAAAGTGCTGGGAT CCAGGCTGGTCTCAAACTCCTGGGCTCAAGTAGTCCACCGTCATAGCCTCTCAAAGTGCTGGGAT T C SNX4 Ensembl:ENSG00000114520 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1439946388 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3042,RMVar_hsa_circ_266705,RMVar_hsa_circ_330096,RMVar_hsa_circ_91232,RMVar_hsa_circ_220893,RMVar_hsa_circ_8244,RMVar_hsa_circ_38805,RMVar_hsa_circ_105641,RMVar_hsa_circ_360162,RMVar_hsa_circ_220899,RMVar_hsa_circ_41436,RMVar_hsa_circ_13062,RMVar_hsa_circ_56237,RMVar_hsa_circ_344814,RMVar_hsa_circ_220900,RMVar_hsa_circ_71103,RMVar_hsa_circ_220901 41354 RMVar_ID_41354 Human_SNP_ID_151977584 A-to-I Human chr3 - 125464736 125464736 125464736 TTTGTCTCAAAAAAACCAAAACTACAAAAATTAGCAGGGAGTGGTGGCATGTACCTGTACTCCCA TTTGTCTCAAAAAAACCAAAACTACAAAAATTGGCAGGGAGTGGTGGCATGTACCTGTACTCCCA T C SNX4 Ensembl:ENSG00000114520 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs535704417 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14599814 RMVar_hsa_circ_3042,RMVar_hsa_circ_266705,RMVar_hsa_circ_330096,RMVar_hsa_circ_91232,RMVar_hsa_circ_220893,RMVar_hsa_circ_8244,RMVar_hsa_circ_38805,RMVar_hsa_circ_105641,RMVar_hsa_circ_360162,RMVar_hsa_circ_220899,RMVar_hsa_circ_41436,RMVar_hsa_circ_13062,RMVar_hsa_circ_56237,RMVar_hsa_circ_344814,RMVar_hsa_circ_220900,RMVar_hsa_circ_71103,RMVar_hsa_circ_220901 41355 RMVar_ID_41355 Human_SNP_ID_151977769 A-to-I Human chr3 - 125465521 125465521 125465521 TACTAGGCCGGGCACAGTGTATCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGTGAA TACTAGGCCGGGCACAGTGTATCACACCTGTAGTCCCAGCACTTTGGGAGGCTGAGGCGGGTGAA T C SNX4 Ensembl:ENSG00000114520 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs909137795 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3042,RMVar_hsa_circ_266705,RMVar_hsa_circ_330096,RMVar_hsa_circ_91232,RMVar_hsa_circ_220893,RMVar_hsa_circ_8244,RMVar_hsa_circ_38805,RMVar_hsa_circ_105641,RMVar_hsa_circ_360162,RMVar_hsa_circ_220899,RMVar_hsa_circ_41436,RMVar_hsa_circ_13062,RMVar_hsa_circ_56237,RMVar_hsa_circ_344814,RMVar_hsa_circ_220900,RMVar_hsa_circ_71103,RMVar_hsa_circ_220901 41356 RMVar_ID_41356 Human_SNP_ID_151978344 A-to-I Human chr3 - 125467672 125467672 125467672 GCAGTGGCTCACGCCTGTAATCCCAGCACTGTAGAAGGCTGAGGTGGGCAGATCTCTTGAGCCTA GCAGTGGCTCACGCCTGTAATCCCAGCACTGTGGAAGGCTGAGGTGGGCAGATCTCTTGAGCCTA T C SNX4 Ensembl:ENSG00000114520 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1196715828 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14599832,Human_RBP_ID_25766198 RMVar_hsa_circ_3042,RMVar_hsa_circ_266705,RMVar_hsa_circ_330096,RMVar_hsa_circ_91232,RMVar_hsa_circ_220893,RMVar_hsa_circ_8244,RMVar_hsa_circ_38805,RMVar_hsa_circ_105641,RMVar_hsa_circ_360162,RMVar_hsa_circ_220899,RMVar_hsa_circ_41436,RMVar_hsa_circ_13062,RMVar_hsa_circ_56237,RMVar_hsa_circ_344814,RMVar_hsa_circ_220900,RMVar_hsa_circ_71103,RMVar_hsa_circ_220901 41357 RMVar_ID_41357 Human_SNP_ID_151988151 A-to-I Human chr3 - 125506985 125506985 125506985 GTTGGCTAGACTGGTCTTGAACTCCTGACCTCAGGTGACCTGCCCGCCTCAGCCTCCCAAAGTGC GTTGGCTAGACTGGTCTTGAACTCCTGACCTCCGGTGACCTGCCCGCCTCAGCCTCCCAAAGTGC T G SNX4 Ensembl:ENSG00000114520 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs933768950 Functional Loss SNV dbSNP153 33..33 33 - - - 41358 RMVar_ID_41358 Human_SNP_ID_151988185 A-to-I Human chr3 - 125507125 125507125 125507125 TTGCTCACTGCAACCTCCGCCTCCTGGGTTCAAGTAATTCTCCATGCCTCAGTCTCTGAGTAGCT TTGCTCACTGCAACCTCCGCCTCCTGGGTTCAGGTAATTCTCCATGCCTCAGTCTCTGAGTAGCT T C SNX4 Ensembl:ENSG00000114520 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1000812518 Functional Loss SNV dbSNP153 33..33 33 - - - 41359 RMVar_ID_41359 Human_SNP_ID_151989739 A-to-I Human chr3 - 125513373 125513373 125513373 TAGTCTGTTCGGGCTGCTATAACAAGGTACCAAAGACTGAGTGGCTTATAAACAATAGCAATGAA TAGTCTGTTCGGGCTGCTATAACAAGGTACCAGAGACTGAGTGGCTTATAAACAATAGCAATGAA T C SNX4 Ensembl:ENSG00000114520 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs958457502 Functional Loss SNV dbSNP153 33..33 33 - - - 41360 RMVar_ID_41360 Human_SNP_ID_151990093 A-to-I Human chr3 - 125514939 125514939 125514939 AAGCATTGGGCTGGATGCAGTGGCTCACACTTATAATCTCAGGACTTTAGGAGGCTGAGGCCCAT AAGCATTGGGCTGGATGCAGTGGCTCACACTTGTAATCTCAGGACTTTAGGAGGCTGAGGCCCAT T C SNX4 Ensembl:ENSG00000114520 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1047499849 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14600556 41361 RMVar_ID_41361 Human_SNP_ID_151990275 A-to-I Human chr3 - 125515615 125515615 125515615 TGTTGCCCAGGCTGGAGTGCAATGGCATGATCATGGCTCACTGCAGCCTTGACCTACTGGTCTCA TGTTGCCCAGGCTGGAGTGCAATGGCATGATCGTGGCTCACTGCAGCCTTGACCTACTGGTCTCA T C SNX4 Ensembl:ENSG00000114520 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1003598304 Functional Loss SNV dbSNP153 33..33 33 - - - 41362 RMVar_ID_41362 Human_SNP_ID_151990276 A-to-I Human chr3 - 125515615 125515615 125515615 TGTTGCCCAGGCTGGAGTGCAATGGCATGATCATGGCTCACTGCAGCCTTGACCTACTGGTCTCA TGTTGCCCAGGCTGGAGTGCAATGGCATGATCCTGGCTCACTGCAGCCTTGACCTACTGGTCTCA T G SNX4 Ensembl:ENSG00000114520 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1003598304 Functional Loss SNV dbSNP153 33..33 33 - - - 41363 RMVar_ID_41363 Human_SNP_ID_151999306 A-to-I Human chr3 - 125552415 125552415 125552415 TGCCAAAAAGCGAGGTAGCATCCAGTGTTTTTAGCAGTTCTTCCACCCAGGGAGTCACAAATCAT TGCCAAAAAGCGAGGTAGCATCCAGTGTTTTTGGCAGTTCTTCCACCCAGGGAGTCACAAATCAT T C OSBPL11 Ensembl:ENSG00000144909 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1454749465 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5730,RMVar_hsa_circ_88995,RMVar_hsa_circ_220914,RMVar_hsa_circ_266911,RMVar_hsa_circ_281176,RMVar_hsa_circ_354518,RMVar_hsa_circ_59945,RMVar_hsa_circ_22451,RMVar_hsa_circ_324261,RMVar_hsa_circ_44802,RMVar_hsa_circ_8093,RMVar_hsa_circ_343143 41364 RMVar_ID_41364 Human_SNP_ID_152012213 A-to-I Human chr3 + 125604149 125604134 125604149 CCACCCGCCTCGGCTTCCCAAGTGCTGGGATTACAGGTATGAGCCACCATGCCTAGCTGAGATGG CCACCCGCCTCGGCTTCC_______________CAGGTATGAGCCACCATGCCTAGCTGAGATGG CCAAGTGCTGGGATTA C lnc-ROPN1B-13,lnc-ROPN1B-13:2 RNACentral:URS00008BDDD0,RNACentral:URS0000D57FFA lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1470919866 Functional Loss DEL dbSNP153 19..33 33 - - - 41365 RMVar_ID_41365 Human_SNP_ID_152116666 A-to-I Human chr3 - 125907966 125907966 125907966 CAGCATGGCCAACATGGTGAAACCCTCTCTCTACAGAAAATAGAAAAATTAGCTGGGCCTAGTGA CAGCATGGCCAACATGGTGAAACCCTCTCTCTGCAGAAAATAGAAAAATTAGCTGGGCCTAGTGA T C LINC02614,AC092903.2 Ensembl:ENSG00000241288,Ensembl:ENSG00000248787 lincRNA,lincRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1241875626 Functional Loss SNV dbSNP153 33..33 33 - - - 41366 RMVar_ID_41366 Human_SNP_ID_152116868 A-to-I Human chr3 - 125908495 125908495 125908495 CACTGCAGCCTCAAAATTCCTGGGCTCAAGCAATCCACCCACATCAGCTTCCCAAGTAGTTGGGA CACTGCAGCCTCAAAATTCCTGGGCTCAAGCAGTCCACCCACATCAGCTTCCCAAGTAGTTGGGA T C LINC02614,AC092903.2 Ensembl:ENSG00000241288,Ensembl:ENSG00000248787 lincRNA,lincRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355030951 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5102260 Human_Splice_Rec_477088,Human_Splice_Rec_477089,Human_Splice_Rec_477098,Human_Splice_Rec_477099,Human_Splice_Rec_477116,Human_Splice_Rec_477117,Human_Splice_Rec_477119 RMVar_hsa_circ_50238 41367 RMVar_ID_41367 Human_SNP_ID_152143366 A-to-I Human chr3 - 126006582 126006578 126006582 TCCCAAGCCTCAGAACTCTTGAGCTGTGGCTTACTTGCTGTCTTCACCAGGTTCAAGCTCCGTGG TCCCAAGCCTCAGAACTCTTGAGCTGTGGCTT____GCTGTCTTCACCAGGTTCAAGCTCCGTGG CAAGT C SLC41A3 Ensembl:ENSG00000114544 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1559797380 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_588035 Human_Splice_Rec_477290 Human_miRNA_ID_2723282 RMVar_hsa_circ_76838,RMVar_hsa_circ_220932 41368 RMVar_ID_41368 Human_SNP_ID_152143367 A-to-I Human chr3 - 126006582 126006582 126006582 TCCCAAGCCTCAGAACTCTTGAGCTGTGGCTTACTTGCTGTCTTCACCAGGTTCAAGCTCCGTGG TCCCAAGCCTCAGAACTCTTGAGCTGTGGCTTTCTTGCTGTCTTCACCAGGTTCAAGCTCCGTGG T A SLC41A3 Ensembl:ENSG00000114544 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1015322341 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_588035 Human_Splice_Rec_477290 Human_miRNA_ID_2723282 RMVar_hsa_circ_76838,RMVar_hsa_circ_220932 41369 RMVar_ID_41369 Human_SNP_ID_152256583 A-to-I Human chr3 - 126455831 126455831 126455831 CCCAGCTAATTTTTTTTTTTTGTATTTTTAGTAGAGACGGGGGTTTCACCGTATTAGCCAGGATG CCCAGCTAATTTTTTTTTTTTGTATTTTTAGTGGAGACGGGGGTTTCACCGTATTAGCCAGGATG T C ZXDC Ensembl:ENSG00000070476 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1347705920 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110260,RMVar_hsa_circ_266628,RMVar_hsa_circ_220939 41370 RMVar_ID_41370 Human_SNP_ID_152256831 A-to-I Human chr3 - 126456784 126456782 126456784 TAACTATCTTGCAGTAGATGCTTTGAGACTGTATGTGGGGCTTGGGGGTCCCTAAGACCACCTTC TAACTATCTTGCAGTAGATGCTTTGAGACTGT__GTGGGGCTTGGGGGTCCCTAAGACCACCTTC CAT C ZXDC Ensembl:ENSG00000070476 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1560096489 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_110260,RMVar_hsa_circ_266628,RMVar_hsa_circ_220939 41371 RMVar_ID_41371 Human_SNP_ID_152256832 A-to-I Human chr3 - 126456784 126456784 126456784 TAACTATCTTGCAGTAGATGCTTTGAGACTGTATGTGGGGCTTGGGGGTCCCTAAGACCACCTTC TAACTATCTTGCAGTAGATGCTTTGAGACTGTTTGTGGGGCTTGGGGGTCCCTAAGACCACCTTC T A ZXDC Ensembl:ENSG00000070476 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs796583 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110260,RMVar_hsa_circ_266628,RMVar_hsa_circ_220939 41372 RMVar_ID_41372 Human_SNP_ID_152256833 A-to-I Human chr3 - 126456784 126456784 126456784 TAACTATCTTGCAGTAGATGCTTTGAGACTGTATGTGGGGCTTGGGGGTCCCTAAGACCACCTTC TAACTATCTTGCAGTAGATGCTTTGAGACTGTGTGTGGGGCTTGGGGGTCCCTAAGACCACCTTC T C ZXDC Ensembl:ENSG00000070476 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs796583 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110260,RMVar_hsa_circ_266628,RMVar_hsa_circ_220939 41373 RMVar_ID_41373 Human_SNP_ID_152257238 A-to-I Human chr3 - 126458322 126458322 126458322 TGAGGCAGGAGAATCGCTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCCGAGATTGTGCCACTGT TGAGGCAGGAGAATCGCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCCGAGATTGTGCCACTGT T C ZXDC Ensembl:ENSG00000070476 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs969744498 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110260,RMVar_hsa_circ_266628,RMVar_hsa_circ_220939 41374 RMVar_ID_41374 Human_SNP_ID_152257255 A-to-I Human chr3 - 126458374 126458374 126458374 AAATTAGCCAGGCGTGGTGGCACGTGTCTGTAATCCTAGCTACTTGGGAGGCTGAGGCAGGAGAA AAATTAGCCAGGCGTGGTGGCACGTGTCTGTATTCCTAGCTACTTGGGAGGCTGAGGCAGGAGAA T A ZXDC Ensembl:ENSG00000070476 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs955470630 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110260,RMVar_hsa_circ_266628,RMVar_hsa_circ_220939 41375 RMVar_ID_41375 Human_SNP_ID_152259218 A-to-I Human chr3 - 126465607 126465606 126465607 AAGAATGTTTCACTTTGTTGACTTTCCCTAGCATATGTCCCCTAAGCCTGTGTCTCTCACTGGGA AAGAATGTTTCACTTTGTTGACTTTCCCTAGC_TATGTCCCCTAAGCCTGTGTCTCTCACTGGGA AT A ZXDC Ensembl:ENSG00000070476 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1469156686 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_20812062 RMVar_hsa_circ_300820,RMVar_hsa_circ_110260,RMVar_hsa_circ_266628,RMVar_hsa_circ_220939,RMVar_hsa_circ_329747,RMVar_hsa_circ_116311,RMVar_hsa_circ_283869,RMVar_hsa_circ_220940,RMVar_hsa_circ_21678 41376 RMVar_ID_41376 Human_SNP_ID_152259219 A-to-I Human chr3 - 126465607 126465607 126465607 AAGAATGTTTCACTTTGTTGACTTTCCCTAGCATATGTCCCCTAAGCCTGTGTCTCTCACTGGGA AAGAATGTTTCACTTTGTTGACTTTCCCTAGCGTATGTCCCCTAAGCCTGTGTCTCTCACTGGGA T C ZXDC Ensembl:ENSG00000070476 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4679245 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20812062 GWAS_ID_4780,GWAS_ID_4781,GWAS_ID_4782,GWAS_ID_4783,GWAS_ID_4784 RMVar_hsa_circ_300820,RMVar_hsa_circ_110260,RMVar_hsa_circ_266628,RMVar_hsa_circ_220939,RMVar_hsa_circ_329747,RMVar_hsa_circ_116311,RMVar_hsa_circ_283869,RMVar_hsa_circ_220940,RMVar_hsa_circ_21678 41377 RMVar_ID_41377 Human_SNP_ID_152294176 A-to-I Human chr3 - 126595947 126595947 126595947 TCGAGACTGAGTCTTACTCTGTCACCCAGGCTAGAGTGCAGTGGCACGATCTTGGCTCACTGCAA TCGAGACTGAGTCTTACTCTGTCACCCAGGCTGGAGTGCAGTGGCACGATCTTGGCTCACTGCAA T C AC024558.2 Ensembl:ENSG00000288436 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1222590797 Functional Loss SNV dbSNP153 33..33 33 - - - 41378 RMVar_ID_41378 Human_SNP_ID_152294311 A-to-I Human chr3 - 126596408 126596408 126596408 CACCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGACATGAGCCACCACACTCGCCAATCAATT CACCCACCTCGGCCTCCCAAAGTGCTGGGATTGCAGACATGAGCCACCACACTCGCCAATCAATT T C AC024558.2 Ensembl:ENSG00000288436 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1188106812 Functional Loss SNV dbSNP153 33..33 33 - - - 41379 RMVar_ID_41379 Human_SNP_ID_152294354 A-to-I Human chr3 - 126596576 126596576 126596576 TCACTGCAACCTCCACTTCCTGGGTTCACACAATTCTCCTGCCTTAGCCTCCTGAGTAGCTGAGA TCACTGCAACCTCCACTTCCTGGGTTCACACATTTCTCCTGCCTTAGCCTCCTGAGTAGCTGAGA T A AC024558.2 Ensembl:ENSG00000288436 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs773921671 Functional Loss SNV dbSNP153 33..33 33 - - - 41380 RMVar_ID_41380 Human_SNP_ID_152294355 A-to-I Human chr3 - 126596576 126596576 126596576 TCACTGCAACCTCCACTTCCTGGGTTCACACAATTCTCCTGCCTTAGCCTCCTGAGTAGCTGAGA TCACTGCAACCTCCACTTCCTGGGTTCACACAGTTCTCCTGCCTTAGCCTCCTGAGTAGCTGAGA T C AC024558.2 Ensembl:ENSG00000288436 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs773921671 Functional Loss SNV dbSNP153 33..33 33 - - - 41381 RMVar_ID_41381 Human_SNP_ID_152312417 A-to-I Human chr3 - 126672776 126672776 126672776 GGTGGAAGGCACATTCTGGACACACTGGAACCAGGAGACCAAGCAGTTCTTCCTCCAGTTCCACT GGTGGAAGGCACATTCTGGACACACTGGAACCGGGAGACCAAGCAGTTCTTCCTCCAGTTCCACT T C AC078867.1 Ensembl:ENSG00000248850 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1238759268 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8264894,Human_RBP_ID_17089531 41382 RMVar_ID_41382 Human_SNP_ID_152312418 A-to-I Human chr3 - 126672776 126672776 126672776 GGTGGAAGGCACATTCTGGACACACTGGAACCAGGAGACCAAGCAGTTCTTCCTCCAGTTCCACT GGTGGAAGGCACATTCTGGACACACTGGAACCCGGAGACCAAGCAGTTCTTCCTCCAGTTCCACT T G AC078867.1 Ensembl:ENSG00000248850 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1238759268 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8264894,Human_RBP_ID_17089531 41383 RMVar_ID_41383 Human_SNP_ID_152543300 A-to-I Human chr3 - 127583782 127583782 127583782 CCTGTAGCCCCAGCTACTCGGGAGGCTGAGGCAGGGGAATCGCTTGAACCTGGGAGGCAGAGGTT CCTGTAGCCCCAGCTACTCGGGAGGCTGAGGCGGGGGAATCGCTTGAACCTGGGAGGCAGAGGTT T C TPRA1 Ensembl:ENSG00000163870 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1472371579 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33754,RMVar_hsa_circ_82816,RMVar_hsa_circ_220991,RMVar_hsa_circ_86441,RMVar_hsa_circ_220994 41384 RMVar_ID_41384 Human_SNP_ID_152546452 A-to-I Human chr3 - 127596208 127596208 127596208 AGGCGTAGTGGCGCATGCCTGTAATCCCAACTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAA AGGCGTAGTGGCGCATGCCTGTAATCCCAACTGCTCAGGAGGCTGAGGCAGGAGAATCACTTGAA T C TPRA1 Ensembl:ENSG00000163870 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1044582585 Functional Loss SNV dbSNP153 33..33 33 - - - 41385 RMVar_ID_41385 Human_SNP_ID_152546876 A-to-I Human chr3 - 127598079 127598062 127598080 AACAGAGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAAGCCGAGGTGGGCGG AACAGAGGCCGGGCGCGGTGGCTCACGCCTG__________________AAGCCGAGGTGGGCGG TCCCAAAGTGCTGGGATTA T TPRA1 Ensembl:ENSG00000163870 Protein coding 5'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1240465689 Functional Loss DEL dbSNP153 32..49 33 - - - Human_Splice_Rec_478911,Human_Splice_Rec_479067 41386 RMVar_ID_41386 Human_SNP_ID_152584566 A-to-I Human chr3 - 127742952 127742952 127742952 AAATTACACGGGCATGGTGGTGGGCACCTGTAATCCCAGCTACTCGAGAGGCTGAGGCAGGAGAA AAATTACACGGGCATGGTGGTGGGCACCTGTATTCCCAGCTACTCGAGAGGCTGAGGCAGGAGAA T A MGLL Ensembl:ENSG00000074416 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956259855 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84807,RMVar_hsa_circ_101277,RMVar_hsa_circ_221014,RMVar_hsa_circ_221017,RMVar_hsa_circ_325121,RMVar_hsa_circ_221021,RMVar_hsa_circ_2051,RMVar_hsa_circ_334322 41387 RMVar_ID_41387 Human_SNP_ID_152598341 A-to-I Human chr3 - 127801114 127801114 127801114 TATTTTTACTAGAGATGGGGTTTCACCATGTTAGTCAGGCTGGTCTAGAACTCCTGACCTTAGGC TATTTTTACTAGAGATGGGGTTTCACCATGTTGGTCAGGCTGGTCTAGAACTCCTGACCTTAGGC T C MGLL Ensembl:ENSG00000074416 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1226721061 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84807,RMVar_hsa_circ_221017,RMVar_hsa_circ_2051 41388 RMVar_ID_41388 Human_SNP_ID_152659353 A-to-I Human chr3 + 128065835 128065835 128065835 CTCGACTCGACTCACTGCAACCTCCGCCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCG CTCGACTCGACTCACTGCAACCTCCGCCTCCCTGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCG A T SEC61A1 Ensembl:ENSG00000058262 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs796186869 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14607760 RMVar_hsa_circ_121564,RMVar_hsa_circ_12871,RMVar_hsa_circ_85911,RMVar_hsa_circ_221029,RMVar_hsa_circ_20434,RMVar_hsa_circ_221030,RMVar_hsa_circ_377074,RMVar_hsa_circ_87757,RMVar_hsa_circ_221034 41389 RMVar_ID_41389 Human_SNP_ID_152660754 A-to-I Human chr3 + 128071406 128071406 128071406 CAGAGGGGCAGGGCCTCCCCCAGCCCACGCTTAGGAATGCTTGGCCTCTGGCAGGCAGGCAGCTG CAGAGGGGCAGGGCCTCCCCCAGCCCACGCTTGGGAATGCTTGGCCTCTGGCAGGCAGGCAGCTG A G SEC61A1 Ensembl:ENSG00000058262 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1042995 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_588523,Human_RBP_ID_1617133,Human_RBP_ID_7117360,Human_RBP_ID_8557836,Human_RBP_ID_17702753,Human_RBP_ID_27497742 Human_miRNA_ID_1190222,Human_miRNA_ID_1952892 RMVar_hsa_circ_85911,RMVar_hsa_circ_221030,RMVar_hsa_circ_87757,RMVar_hsa_circ_109992,RMVar_hsa_circ_221034,RMVar_hsa_circ_221036,RMVar_hsa_circ_96417,RMVar_hsa_circ_221037,RMVar_hsa_circ_221038,RMVar_hsa_circ_99254 41390 RMVar_ID_41390 Human_SNP_ID_152660755 A-to-I Human chr3 + 128071406 128071406 128071406 CAGAGGGGCAGGGCCTCCCCCAGCCCACGCTTAGGAATGCTTGGCCTCTGGCAGGCAGGCAGCTG CAGAGGGGCAGGGCCTCCCCCAGCCCACGCTTTGGAATGCTTGGCCTCTGGCAGGCAGGCAGCTG A T SEC61A1 Ensembl:ENSG00000058262 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1042995 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_588523,Human_RBP_ID_1617133,Human_RBP_ID_7117360,Human_RBP_ID_8557836,Human_RBP_ID_17702753,Human_RBP_ID_27497742 Human_miRNA_ID_1190222,Human_miRNA_ID_1952892 RMVar_hsa_circ_85911,RMVar_hsa_circ_221030,RMVar_hsa_circ_87757,RMVar_hsa_circ_109992,RMVar_hsa_circ_221034,RMVar_hsa_circ_221036,RMVar_hsa_circ_96417,RMVar_hsa_circ_221037,RMVar_hsa_circ_221038,RMVar_hsa_circ_99254 41391 RMVar_ID_41391 Human_SNP_ID_152709446 A-to-I Human chr3 + 128286186 128286186 128286186 TGAATTTTTACTGCTGTATGGGGTCCTATTACATGACTTGACTATAGTTCATGAGGGACATTCCC TGAATTTTTACTGCTGTATGGGGTCCTATTACGTGACTTGACTATAGTTCATGAGGGACATTCCC A G EEFSEC Ensembl:ENSG00000132394 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1187938447 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17573830 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 41392 RMVar_ID_41392 Human_SNP_ID_152709447 A-to-I Human chr3 + 128286197 128286195 128286197 TGCTGTATGGGGTCCTATTACATGACTTGACTATAGTTCATGAGGGACATTCCCAGAGCATTTTG TGCTGTATGGGGTCCTATTACATGACTTGAC__TAGTTCATGAGGGACATTCCCAGAGCATTTTG CTA C EEFSEC Ensembl:ENSG00000132394 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1486545811 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_17573830 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 41393 RMVar_ID_41393 Human_SNP_ID_152709448 A-to-I Human chr3 + 128286197 128286197 128286197 TGCTGTATGGGGTCCTATTACATGACTTGACTATAGTTCATGAGGGACATTCCCAGAGCATTTTG TGCTGTATGGGGTCCTATTACATGACTTGACTGTAGTTCATGAGGGACATTCCCAGAGCATTTTG A G EEFSEC Ensembl:ENSG00000132394 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1283709003 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17573830 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 41394 RMVar_ID_41394 Human_SNP_ID_152795965 A-to-I Human chr3 - 128633318 128633318 128633318 TGGGGCTTGAGGTGGGAGGATTGCTTGAGCCCAGGAGGTTGAGACTGCATTGAGCCAAGATTGTG TGGGGCTTGAGGTGGGAGGATTGCTTGAGCCCGGGAGGTTGAGACTGCATTGAGCCAAGATTGTG T C RPN1 Ensembl:ENSG00000163902 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1184242642 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25695068 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_221080,RMVar_hsa_circ_315210,RMVar_hsa_circ_345550,RMVar_hsa_circ_221079 41395 RMVar_ID_41395 Human_SNP_ID_152796091 A-to-I Human chr3 - 128633820 128633820 128633820 CATCACCACACCTGGCTAATTTTTCTATTTTTAGTAGAGACGGGGTTTCACCATATTGGCCAGGC CATCACCACACCTGGCTAATTTTTCTATTTTTTGTAGAGACGGGGTTTCACCATATTGGCCAGGC T A RPN1 Ensembl:ENSG00000163902 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1254136897 Functional Loss SNV dbSNP153 33..33 33 - - - 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_221080,RMVar_hsa_circ_315210,RMVar_hsa_circ_345550,RMVar_hsa_circ_221079 41396 RMVar_ID_41396 Human_SNP_ID_152797156 A-to-I Human chr3 - 128637040 128637040 128637040 TAGAGACGGGATCTTGCTTTATTGCCCAGGCTAGTCTCAAACTCCTGGGCCCAGGTGATCTTCCT TAGAGACGGGATCTTGCTTTATTGCCCAGGCTCGTCTCAAACTCCTGGGCCCAGGTGATCTTCCT T G RPN1 Ensembl:ENSG00000163902 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1229750113 Functional Loss SNV dbSNP153 33..33 33 - - - 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_221080,RMVar_hsa_circ_315210,RMVar_hsa_circ_345550,RMVar_hsa_circ_221079 41397 RMVar_ID_41397 Human_SNP_ID_152797861 A-to-I Human chr3 - 128639653 128639653 128639653 AACCCAGCAGGCGGAGGTTGCGGTGAGCCAAGATTGTGCCATTTCACTCCAGCCTGGGCTACAAG AACCCAGCAGGCGGAGGTTGCGGTGAGCCAAGGTTGTGCCATTTCACTCCAGCCTGGGCTACAAG T C RPN1 Ensembl:ENSG00000163902 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1392636779 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 41398 RMVar_ID_41398 Human_SNP_ID_152822876 A-to-I Human chr3 + 128731746 128731746 128731746 AGTGTATCTTTCGGCCGGGGGCGATGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGA AGTGTATCTTTCGGCCGGGGGCGATGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGA A G RAB7A Ensembl:ENSG00000075785 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444187043 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42399,RMVar_hsa_circ_112866,RMVar_hsa_circ_221084 41399 RMVar_ID_41399 Human_SNP_ID_152822899 A-to-I Human chr3 + 128731841 128731841 128731841 CATCCTGGCCAACGTGGTGAAACCCCGTCTATACTAAAAATATAAAAATTAGCTGGGCATAGTGG CATCCTGGCCAACGTGGTGAAACCCCGTCTATCCTAAAAATATAAAAATTAGCTGGGCATAGTGG A C RAB7A Ensembl:ENSG00000075785 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1333266688 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42399,RMVar_hsa_circ_112866,RMVar_hsa_circ_221084 41400 RMVar_ID_41400 Human_SNP_ID_152824889 A-to-I Human chr3 + 128739462 128739462 128739462 TTGAACCTGAGAGGCAGAGGTTGCAGTGAGCCAAGATCGCGCCACTGCACTCCAGCCTTGCCAAC TTGAACCTGAGAGGCAGAGGTTGCAGTGAGCCGAGATCGCGCCACTGCACTCCAGCCTTGCCAAC A G RAB7A Ensembl:ENSG00000075785 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1274928756 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42399,RMVar_hsa_circ_112866,RMVar_hsa_circ_221084 41401 RMVar_ID_41401 Human_SNP_ID_152826288 A-to-I Human chr3 + 128744168 128744168 128744168 CCAGCTACTTGGGAGGCTAGAGTGGGAGGATCACTTGAGCCCTGCGGTTGGAGGCTGCATTGAGT CCAGCTACTTGGGAGGCTAGAGTGGGAGGATCCCTTGAGCCCTGCGGTTGGAGGCTGCATTGAGT A C RAB7A Ensembl:ENSG00000075785 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1173209149 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17573831 RMVar_hsa_circ_42399,RMVar_hsa_circ_112866,RMVar_hsa_circ_221084 41402 RMVar_ID_41402 Human_SNP_ID_152826623 A-to-I Human chr3 + 128745387 128745386 128745388 TTAAGAATCATCTTTTTTTTTGTTTTGGAGACAGAGTTTTGCTTTGTTGCCCAGGCTGGAGTGCA TTAAGAATCATCTTTTTTTTTGTTTTGGAGAC__AGTTTTGCTTTGTTGCCCAGGCTGGAGTGCA CAG C RAB7A Ensembl:ENSG00000075785 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1338019184 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_14611032 RMVar_hsa_circ_42399,RMVar_hsa_circ_112866,RMVar_hsa_circ_221084 41403 RMVar_ID_41403 Human_SNP_ID_152826624 A-to-I Human chr3 + 128745389 128745389 128745389 AAGAATCATCTTTTTTTTTGTTTTGGAGACAGAGTTTTGCTTTGTTGCCCAGGCTGGAGTGCAGT AAGAATCATCTTTTTTTTTGTTTTGGAGACAGTGTTTTGCTTTGTTGCCCAGGCTGGAGTGCAGT A T RAB7A Ensembl:ENSG00000075785 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs759922373 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42399,RMVar_hsa_circ_112866,RMVar_hsa_circ_221084 41404 RMVar_ID_41404 Human_SNP_ID_152829734 A-to-I Human chr3 + 128757589 128757589 128757589 TTACCCAGGCTGGAGTATAGTGGCATGATCTCAGCTCACTGCAACCTCTGCCTCCTGGGTTACAA TTACCCAGGCTGGAGTATAGTGGCATGATCTCGGCTCACTGCAACCTCTGCCTCCTGGGTTACAA A G RAB7A Ensembl:ENSG00000075785 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432824210 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42399,RMVar_hsa_circ_112866,RMVar_hsa_circ_221084 41405 RMVar_ID_41405 Human_SNP_ID_152835701 A-to-I Human chr3 + 128779156 128779156 128779156 CATTGTGGGGCTGGGTACGGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCTGAGGCGGGC CATTGTGGGGCTGGGTACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGC A G RAB7A Ensembl:ENSG00000075785 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1360976555 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42399,RMVar_hsa_circ_112866,RMVar_hsa_circ_221084 41406 RMVar_ID_41406 Human_SNP_ID_152835744 A-to-I Human chr3 + 128779340 128779340 128779340 GGAGGCTGAAGAGTTGCTTGAGCCCAGGAGACAAAGGTTGCAGTGAGCCGAGATCACGCCACTGC GGAGGCTGAAGAGTTGCTTGAGCCCAGGAGACGAAGGTTGCAGTGAGCCGAGATCACGCCACTGC A G RAB7A Ensembl:ENSG00000075785 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1369752362 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42399,RMVar_hsa_circ_112866,RMVar_hsa_circ_221084 41407 RMVar_ID_41407 Human_SNP_ID_152839943 A-to-I Human chr3 + 128796401 128796401 128796401 TTGAGCCCAGGAGTTTGAGGCTGTAGCAAGCTATGATCATGCCGTTGCACTGCAGCCCGAGTGAC TTGAGCCCAGGAGTTTGAGGCTGTAGCAAGCTGTGATCATGCCGTTGCACTGCAGCCCGAGTGAC A G RAB7A Ensembl:ENSG00000075785 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335504744 Functional Loss SNV dbSNP153 33..33 33 - - - 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_221087,RMVar_hsa_circ_221089,RMVar_hsa_circ_221090,RMVar_hsa_circ_221088 41408 RMVar_ID_41408 Human_SNP_ID_152843693 A-to-I Human chr3 + 128811204 128811204 128811204 GCTGATACGCAGTGGTGCAATCATCACTCGCTATAACCTCCAACTTCTGGGCTCCAGCAGTCTTC GCTGATACGCAGTGGTGCAATCATCACTCGCTGTAACCTCCAACTTCTGGGCTCCAGCAGTCTTC A G RAB7A Ensembl:ENSG00000075785 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs140101686 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112866,RMVar_hsa_circ_221084,RMVar_hsa_circ_378866,RMVar_hsa_circ_102059,RMVar_hsa_circ_97431,RMVar_hsa_circ_221089,RMVar_hsa_circ_221090,RMVar_hsa_circ_114706,RMVar_hsa_circ_221091,RMVar_hsa_circ_221096,RMVar_hsa_circ_123322,RMVar_hsa_circ_221097 41409 RMVar_ID_41409 Human_SNP_ID_152860198 A-to-I Human chr3 - 128877994 128877994 128877994 GGAACAGAAGACAGCAAGAAAAACTCACTTCAACCCCCTATCATTCCATCTCCAACCCAACCAGT GGAACAGAAGACAGCAAGAAAAACTCACTTCATCCCCCTATCATTCCATCTCCAACCCAACCAGT T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs767357969 Functional Loss SNV dbSNP153 33..33 33 - - - 41410 RMVar_ID_41410 Human_SNP_ID_152860199 A-to-I Human chr3 - 128877994 128877994 128877994 GGAACAGAAGACAGCAAGAAAAACTCACTTCAACCCCCTATCATTCCATCTCCAACCCAACCAGT GGAACAGAAGACAGCAAGAAAAACTCACTTCAGCCCCCTATCATTCCATCTCCAACCCAACCAGT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs767357969 Functional Loss SNV dbSNP153 33..33 33 - - - 41411 RMVar_ID_41411 Human_SNP_ID_152860205 A-to-I Human chr3 - 128878036 128878036 128878036 CAGACCGGTAATCTGGCTCAACAAGTTTTGCAATCCCACCTAGGAACAGAAGACAGCAAGAAAAA CAGACCGGTAATCTGGCTCAACAAGTTTTGCAGTCCCACCTAGGAACAGAAGACAGCAAGAAAAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917941818 Functional Loss SNV dbSNP153 33..33 33 - - - 41412 RMVar_ID_41412 Human_SNP_ID_152860215 A-to-I Human chr3 - 128878058 128878058 128878058 AATGCCACTCTGCTTTTTCACCCAGACCGGTAATCTGGCTCAACAAGTTTTGCAATCCCACCTAG AATGCCACTCTGCTTTTTCACCCAGACCGGTAGTCTGGCTCAACAAGTTTTGCAATCCCACCTAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1391634637 Functional Loss SNV dbSNP153 33..33 33 - - - 41413 RMVar_ID_41413 Human_SNP_ID_152860219 A-to-I Human chr3 - 128878067 128878067 128878067 TCCAGGAAGAATGCCACTCTGCTTTTTCACCCAGACCGGTAATCTGGCTCAACAAGTTTTGCAAT TCCAGGAAGAATGCCACTCTGCTTTTTCACCCGGACCGGTAATCTGGCTCAACAAGTTTTGCAAT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs930308921 Functional Loss SNV dbSNP153 33..33 33 - - - 41414 RMVar_ID_41414 Human_SNP_ID_152860376 A-to-I Human chr3 - 128878727 128878727 128878727 TCGGTCTCCCCAAAAACGGATCGGAATTTTTAAGGATAATTTGGCGAGTAGAAGCTCGGGAAGTG TCGGTCTCCCCAAAAACGGATCGGAATTTTTAGGGATAATTTGGCGAGTAGAAGCTCGGGAAGTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs755348601 Functional Loss SNV dbSNP153 33..33 33 - - - 41415 RMVar_ID_41415 Human_SNP_ID_152860380 A-to-I Human chr3 - 128878747 128878747 128878747 AGGGAGTTTTATTAGCCAAATCGGTCTCCCCAAAAACGGATCGGAATTTTTAAGGATAATTTGGC AGGGAGTTTTATTAGCCAAATCGGTCTCCCCAGAAACGGATCGGAATTTTTAAGGATAATTTGGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041526244 Functional Loss SNV dbSNP153 33..33 33 - - - 41416 RMVar_ID_41416 Human_SNP_ID_152861278 A-to-I Human chr3 + 128881520 128881520 128881520 TCTCATTAGACTCCAGGTCTTCTCACCTACTCAAGGGTAATTCTTTCCTTTCTCTGCATCATTAA TCTCATTAGACTCCAGGTCTTCTCACCTACTCGAGGGTAATTCTTTCCTTTCTCTGCATCATTAA A G ACAD9 Ensembl:ENSG00000177646 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1178490868 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3685580,Human_RBP_ID_20785194,Human_RBP_ID_27044979 RMVar_hsa_circ_78808,RMVar_hsa_circ_221099 41417 RMVar_ID_41417 Human_SNP_ID_152862239 A-to-I Human chr3 + 128885495 128885495 128885495 CTCACCACCACCTCCATCTTTCAGGCTCAAACAGTCCCCCAACTTCAGCCTCCTGAGTTGCTGGA CTCACCACCACCTCCATCTTTCAGGCTCAAACTGTCCCCCAACTTCAGCCTCCTGAGTTGCTGGA A T ACAD9 Ensembl:ENSG00000177646 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1393014447 Functional Loss SNV dbSNP153 33..33 33 - - - 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_221100,RMVar_hsa_circ_221101 41418 RMVar_ID_41418 Human_SNP_ID_152862648 A-to-I Human chr3 + 128887067 128887067 128887067 CATGCCTCAGCTTCCTGAGTAGCTGGAATTATAGCACGCACCGCCACGCCTGGCTAATTTTTGTA CATGCCTCAGCTTCCTGAGTAGCTGGAATTATGGCACGCACCGCCACGCCTGGCTAATTTTTGTA A G ACAD9 Ensembl:ENSG00000177646 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1376740787 Functional Loss SNV dbSNP153 33..33 33 - - - 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_221100,RMVar_hsa_circ_221101 41419 RMVar_ID_41419 Human_SNP_ID_152862761 A-to-I Human chr3 + 128887486 128887486 128887486 AATATTAGCCGGGCATGGTGGTGCGCGCCCATAGTCCCAGCTACTTGGGAGTCTGAGGTGGGAGA AATATTAGCCGGGCATGGTGGTGCGCGCCCATCGTCCCAGCTACTTGGGAGTCTGAGGTGGGAGA A C ACAD9 Ensembl:ENSG00000177646 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs563500364 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25695399 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_221100,RMVar_hsa_circ_221101 41420 RMVar_ID_41420 Human_SNP_ID_152862762 A-to-I Human chr3 + 128887486 128887486 128887486 AATATTAGCCGGGCATGGTGGTGCGCGCCCATAGTCCCAGCTACTTGGGAGTCTGAGGTGGGAGA AATATTAGCCGGGCATGGTGGTGCGCGCCCATGGTCCCAGCTACTTGGGAGTCTGAGGTGGGAGA A G ACAD9 Ensembl:ENSG00000177646 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs563500364 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25695399 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_221100,RMVar_hsa_circ_221101 41421 RMVar_ID_41421 Human_SNP_ID_152863020 A-to-I Human chr3 + 128888305 128888305 128888305 CAAGTAACATCTTAAGTAGTTTTAGGCCAGGTATGGTGGCTCATGCCTGCAATCCCAGCGCTTTG CAAGTAACATCTTAAGTAGTTTTAGGCCAGGTGTGGTGGCTCATGCCTGCAATCCCAGCGCTTTG A G ACAD9 Ensembl:ENSG00000177646 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs528850008 Functional Loss SNV dbSNP153 33..33 33 - - - 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_221100,RMVar_hsa_circ_221101 41422 RMVar_ID_41422 Human_SNP_ID_152863454 A-to-I Human chr3 + 128890046 128890046 128890046 TGGGTTCTCACTATGTTATTCAGGCTGGTCTCAGACTCCTGGGCTCAGGTGATCTTCCTACCTCA TGGGTTCTCACTATGTTATTCAGGCTGGTCTCGGACTCCTGGGCTCAGGTGATCTTCCTACCTCA A G ACAD9 Ensembl:ENSG00000177646 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs994700887 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7118591 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_221100,RMVar_hsa_circ_221101 41423 RMVar_ID_41423 Human_SNP_ID_152863523 A-to-I Human chr3 + 128890269 128890269 128890269 ACCACATCTGGCTAATTTTTGGTATTTTGAGTAGAGAAGGGGCTTCACCATGTTGGCCAGGCCAA ACCACATCTGGCTAATTTTTGGTATTTTGAGTGGAGAAGGGGCTTCACCATGTTGGCCAGGCCAA A G ACAD9 Ensembl:ENSG00000177646 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs13098985 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14613893 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_221100,RMVar_hsa_circ_221101 41424 RMVar_ID_41424 Human_SNP_ID_152871784 A-to-I Human chr3 + 128920329 128920329 128920329 GAAGGCTGAGGCAGGGAGAATTGCTTGAACCCAGGAGGCGGAGTTTGCAGTGAGCCAAGATAGTG GAAGGCTGAGGCAGGGAGAATTGCTTGAACCCGGGAGGCGGAGTTTGCAGTGAGCCAAGATAGTG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs549111232 Functional Loss SNV dbSNP153 33..33 33 - - - 41425 RMVar_ID_41425 Human_SNP_ID_152914500 A-to-I Human chr3 - 129091947 129091947 129091947 CCTGCCTCAGGCACCCGAGTAGCTGGGATTACAGGCCCCCGCCACCACGCCTAGCTAATTTTTTG CCTGCCTCAGGCACCCGAGTAGCTGGGATTACGGGCCCCCGCCACCACGCCTAGCTAATTTTTTG T C ISY1-RAB43,RAB43 Ensembl:ENSG00000261796,Ensembl:ENSG00000172780 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1403019797 Functional Loss SNV dbSNP153 33..33 33 - - - 41426 RMVar_ID_41426 Human_SNP_ID_152914879 A-to-I Human chr3 - 129093355 129093355 129093355 CACCCGTCTCGACCTCTAAAAGTGCTGGGATTACAGGTGTGAGCCACCACACCCAGCCACCAATT CACCCGTCTCGACCTCTAAAAGTGCTGGGATTGCAGGTGTGAGCCACCACACCCAGCCACCAATT T C ISY1-RAB43,RAB43 Ensembl:ENSG00000261796,Ensembl:ENSG00000172780 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1035174005 Functional Loss SNV dbSNP153 33..33 33 - - - 41427 RMVar_ID_41427 Human_SNP_ID_152914898 A-to-I Human chr3 - 129093406 129093406 129093406 TGGGTTTCACCATGTTGGCCAGGATGGTCTCGATCTCCTGACCTCGTGATCCACCCGTCTCGACC TGGGTTTCACCATGTTGGCCAGGATGGTCTCGGTCTCCTGACCTCGTGATCCACCCGTCTCGACC T C ISY1-RAB43,RAB43 Ensembl:ENSG00000261796,Ensembl:ENSG00000172780 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1412433968 Functional Loss SNV dbSNP153 33..33 33 - - - 41428 RMVar_ID_41428 Human_SNP_ID_152914998 A-to-I Human chr3 - 129093838 129093838 129093838 AAAACCACTGCAACCTCTGTCTCCCTGGTTCAAGCGATTCTCCTGCTTCAGCCTCCCGAGTAGCT AAAACCACTGCAACCTCTGTCTCCCTGGTTCAGGCGATTCTCCTGCTTCAGCCTCCCGAGTAGCT T C ISY1-RAB43,RAB43 Ensembl:ENSG00000261796,Ensembl:ENSG00000172780 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs541100275 Functional Loss SNV dbSNP153 33..33 33 - - - 41429 RMVar_ID_41429 Human_SNP_ID_152915021 A-to-I Human chr3 - 129093925 129093925 129093925 CAGGTTGATTCTTTTTTTTGAGACAGAGTCTTACTCAGTCACCCAGGCTGGAGTGCCGTGGCGTG CAGGTTGATTCTTTTTTTTGAGACAGAGTCTTTCTCAGTCACCCAGGCTGGAGTGCCGTGGCGTG T A ISY1-RAB43,RAB43 Ensembl:ENSG00000261796,Ensembl:ENSG00000172780 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs901463645 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22480982 41430 RMVar_ID_41430 Human_SNP_ID_152925162 A-to-I Human chr3 - 129135098 129135096 129135098 GTGAGCCACCTGTCTGGGCCTCCCAAAGCGCTAGGATTACAAGCATGAGCCACTGCGCCCACCTG GTGAGCCACCTGTCTGGGCCTCCCAAAGCGCT__GATTACAAGCATGAGCCACTGCGCCCACCTG CCT C ISY1-RAB43,ISY1 Ensembl:ENSG00000261796,Ensembl:ENSG00000240682 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1220671108 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_45314,RMVar_hsa_circ_76874,RMVar_hsa_circ_378577,RMVar_hsa_circ_221109 41431 RMVar_ID_41431 Human_SNP_ID_152925163 A-to-I Human chr3 - 129135098 129135096 129135099 GTGAGCCACCTGTCTGGGCCTCCCAAAGCGCTAGGATTACAAGCATGAGCCACTGCGCCCACCTG GTGAGCCACCTGTCTGGGCCTCCCAAAGCGC___GATTACAAGCATGAGCCACTGCGCCCACCTG CCTA C ISY1-RAB43,ISY1 Ensembl:ENSG00000261796,Ensembl:ENSG00000240682 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1242018384 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_45314,RMVar_hsa_circ_76874,RMVar_hsa_circ_378577,RMVar_hsa_circ_221109 41432 RMVar_ID_41432 Human_SNP_ID_152926611 A-to-I Human chr3 - 129139767 129139767 129139767 ATGGTGGTGCATGCCTGTACTCCCAGCTACTCAGGAGACTGAGACAGGAGAATTGCTTGAATCTG ATGGTGGTGCATGCCTGTACTCCCAGCTACTCTGGAGACTGAGACAGGAGAATTGCTTGAATCTG T A ISY1-RAB43,ISY1 Ensembl:ENSG00000261796,Ensembl:ENSG00000240682 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs539297831 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45314,RMVar_hsa_circ_76874,RMVar_hsa_circ_378577,RMVar_hsa_circ_221109 41433 RMVar_ID_41433 Human_SNP_ID_152926612 A-to-I Human chr3 - 129139767 129139767 129139767 ATGGTGGTGCATGCCTGTACTCCCAGCTACTCAGGAGACTGAGACAGGAGAATTGCTTGAATCTG ATGGTGGTGCATGCCTGTACTCCCAGCTACTCGGGAGACTGAGACAGGAGAATTGCTTGAATCTG T C ISY1-RAB43,ISY1 Ensembl:ENSG00000261796,Ensembl:ENSG00000240682 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs539297831 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45314,RMVar_hsa_circ_76874,RMVar_hsa_circ_378577,RMVar_hsa_circ_221109 41434 RMVar_ID_41434 Human_SNP_ID_152926923 A-to-I Human chr3 - 129141047 129141047 129141047 GGCATGTCTCACCACACCCAGCTAATTTTTGTATATTTAGTAGAGACAGGGTTTTGCCATGTTGC GGCATGTCTCACCACACCCAGCTAATTTTTGTGTATTTAGTAGAGACAGGGTTTTGCCATGTTGC T C ISY1-RAB43,ISY1 Ensembl:ENSG00000261796,Ensembl:ENSG00000240682 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs567371668 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45314,RMVar_hsa_circ_76874,RMVar_hsa_circ_378577,RMVar_hsa_circ_221109,RMVar_hsa_circ_344670 41435 RMVar_ID_41435 Human_SNP_ID_152928890 A-to-I Human chr3 - 129148850 129148850 129148850 AAAGAAAATATGTAGGGTGGGCATGGTGGCTCACGCCTGTAATCCTAGCAGTTTGGGAGGCCGAG AAAGAAAATATGTAGGGTGGGCATGGTGGCTCGCGCCTGTAATCCTAGCAGTTTGGGAGGCCGAG T C ISY1-RAB43,ISY1 Ensembl:ENSG00000261796,Ensembl:ENSG00000240682 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs972397955 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76874,RMVar_hsa_circ_221109 41436 RMVar_ID_41436 Human_SNP_ID_152930564 A-to-I Human chr3 - 129154333 129154333 129154333 AATTTCTCCCTGGGTTCACCTCCCTGGGTTCAAGCAATTTCTCCTGCCTCAGCCTCCCGAGTAGC AATTTCTCCCTGGGTTCACCTCCCTGGGTTCAGGCAATTTCTCCTGCCTCAGCCTCCCGAGTAGC T C ISY1-RAB43,ISY1 Ensembl:ENSG00000261796,Ensembl:ENSG00000240682 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs368192859 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76874,RMVar_hsa_circ_221109 41437 RMVar_ID_41437 Human_SNP_ID_152930993 A-to-I Human chr3 - 129155873 129155873 129155873 CTACTGAAAATACAAAATTGGCTGGACGTGGTAGCGCATGCTTGTAATCCCAGCTACTTGGGAGG CTACTGAAAATACAAAATTGGCTGGACGTGGTGGCGCATGCTTGTAATCCCAGCTACTTGGGAGG T C ISY1-RAB43,ISY1 Ensembl:ENSG00000261796,Ensembl:ENSG00000240682 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1282556647 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76874,RMVar_hsa_circ_221109 41438 RMVar_ID_41438 Human_SNP_ID_152931120 A-to-I Human chr3 - 129156277 129156277 129156277 CTCCTGCCTCAGCCTCCCGAATAGCTGGGACTACAGGTGCCCACAACCACGCCCGGCTAATTTTT CTCCTGCCTCAGCCTCCCGAATAGCTGGGACTGCAGGTGCCCACAACCACGCCCGGCTAATTTTT T C ISY1-RAB43,ISY1 Ensembl:ENSG00000261796,Ensembl:ENSG00000240682 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs929683168 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76874,RMVar_hsa_circ_221109 41439 RMVar_ID_41439 Human_SNP_ID_152933786 A-to-I Human chr3 - 129164941 129164941 129164941 GCTGGAGTGCTGTGGGAGCGTGATCTTGGCTCACTGCAACCTCCACCTCGCAGGTTCAAGCAATA GCTGGAGTGCTGTGGGAGCGTGATCTTGGCTCGCTGCAACCTCCACCTCGCAGGTTCAAGCAATA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs541724668 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76874,RMVar_hsa_circ_221109 41440 RMVar_ID_41440 Human_SNP_ID_152933846 A-to-I Human chr3 - 129165153 129165153 129165153 CTGTTTTTTTTTTTTTCTTTCTTTTTTGAGACAGAGTCTTGCCCTGTTGCCCAGGTTGGAGTGCA CTGTTTTTTTTTTTTTCTTTCTTTTTTGAGACGGAGTCTTGCCCTGTTGCCCAGGTTGGAGTGCA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs953494933 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76874,RMVar_hsa_circ_221109 41441 RMVar_ID_41441 Human_SNP_ID_152933847 A-to-I Human chr3 - 129165153 129165153 129165153 CTGTTTTTTTTTTTTTCTTTCTTTTTTGAGACAGAGTCTTGCCCTGTTGCCCAGGTTGGAGTGCA CTGTTTTTTTTTTTTTCTTTCTTTTTTGAGACCGAGTCTTGCCCTGTTGCCCAGGTTGGAGTGCA T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs953494933 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76874,RMVar_hsa_circ_221109 41442 RMVar_ID_41442 Human_SNP_ID_152934098 A-to-I Human chr3 - 129165849 129165849 129165849 TTGAACCCGGGAGGTGGAGGTTGCAGTGAGCCAAGATGGTGTCACTGCACTCTAGCTTGGGGGAT TTGAACCCGGGAGGTGGAGGTTGCAGTGAGCCGAGATGGTGTCACTGCACTCTAGCTTGGGGGAT T C - - Other Unknown GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1177765192 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76874,RMVar_hsa_circ_221109 41443 RMVar_ID_41443 Human_SNP_ID_152934875 A-to-I Human chr3 - 129168430 129168430 129168430 ACCACACCCAGCTAATTTTTGTTATTTTTAGTAGAGATGGGGTTTCACTGTGTTGGTCAGGCTGG ACCACACCCAGCTAATTTTTGTTATTTTTAGTGGAGATGGGGTTTCACTGTGTTGGTCAGGCTGG T C CNBP Ensembl:ENSG00000169714 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1317171582 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76874,RMVar_hsa_circ_221109 41444 RMVar_ID_41444 Human_SNP_ID_152935945 A-to-I Human chr3 - 129171923 129171923 129171923 CACCCACCTCGGCCTCCCAAAGTGATGGGATTACTGGCGTGAGCCACCATGCCCAGCTATTTTTT CACCCACCTCGGCCTCCCAAAGTGATGGGATTGCTGGCGTGAGCCACCATGCCCAGCTATTTTTT T C CNBP Ensembl:ENSG00000169714 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1467585688 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25695680 RMVar_hsa_circ_95420,RMVar_hsa_circ_221113 41445 RMVar_ID_41445 Human_SNP_ID_152937195 A-to-I Human chr3 - 129175034 129175034 129175034 AGCCACCACGCCTGCCCTAATTTTGTGTTTTTAGTAGAGATGGAGTTTCACTGTGTTGGTCAGGC AGCCACCACGCCTGCCCTAATTTTGTGTTTTTGGTAGAGATGGAGTTTCACTGTGTTGGTCAGGC T C CNBP Ensembl:ENSG00000169714 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1015298697 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14616619 RMVar_hsa_circ_95420,RMVar_hsa_circ_221113 41446 RMVar_ID_41446 Human_SNP_ID_152937212 A-to-I Human chr3 - 129175088 129175088 129175088 ATTTCCTGACCTCATGATCCGCCTGCCTCCCAAAGTGCTGAGATTACAGGCGTGAGCCACCACGC ATTTCCTGACCTCATGATCCGCCTGCCTCCCAGAGTGCTGAGATTACAGGCGTGAGCCACCACGC T C CNBP Ensembl:ENSG00000169714 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs542780395 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95420,RMVar_hsa_circ_221113 41447 RMVar_ID_41447 Human_SNP_ID_152937224 A-to-I Human chr3 - 129175166 129175166 129175166 GCGCGTTACCACCACGCCTGGGTAATTTTTTTATTTTAGTAGATTTGGGGTTTCACCATGTTGGC GCGCGTTACCACCACGCCTGGGTAATTTTTTTGTTTTAGTAGATTTGGGGTTTCACCATGTTGGC T C CNBP Ensembl:ENSG00000169714 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1006074670 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14616625 RMVar_hsa_circ_95420,RMVar_hsa_circ_221113 41448 RMVar_ID_41448 Human_SNP_ID_152939694 A-to-I Human chr3 - 129183121 129183117 129183121 ATATGGTGAAAGTTGGTCTGTACTAAAAATAAAAAATTAGCCGGGCATGGTGGCGGGCGCATGTA ATATGGTGAAAGTTGGTCTGTACTAAAAATAA____TTAGCCGGGCATGGTGGCGGGCGCATGTA ATTTT A CNBP Ensembl:ENSG00000169714 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202283786 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_8558418,Human_RBP_ID_10066114,Human_RBP_ID_25695791 RMVar_hsa_circ_95420,RMVar_hsa_circ_221113 41449 RMVar_ID_41449 Human_SNP_ID_152939696 A-to-I Human chr3 - 129183121 129183121 129183121 ATATGGTGAAAGTTGGTCTGTACTAAAAATAAAAAATTAGCCGGGCATGGTGGCGGGCGCATGTA ATATGGTGAAAGTTGGTCTGTACTAAAAATAATAAATTAGCCGGGCATGGTGGCGGGCGCATGTA T A CNBP Ensembl:ENSG00000169714 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917040896 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8558418,Human_RBP_ID_10066114,Human_RBP_ID_25695791 RMVar_hsa_circ_95420,RMVar_hsa_circ_221113 41450 RMVar_ID_41450 Human_SNP_ID_152940517 A-to-I Human chr3 + 129185444 129185444 129185444 TTTTAAATTTATTTATTACTATTTTTTGAGACAGGGTCTCCCTCTGTTGCCCAGGCTGGAGTGCT TTTTAAATTTATTTATTACTATTTTTTGAGACTGGGTCTCCCTCTGTTGCCCAGGCTGGAGTGCT A T lnc-COPG1-3,lnc-COPG1-3:2,lnc-COPG1-3:3,lnc-COPG1-3:4,lnc-COPG1-3:5,lnc-COPG1-3:6,lnc-COPG1-3:7,lnc-COPG1-3:8 RNACentral:URS00009B5487,RNACentral:URS0000D5A0B5,RNACentral:URS00009B35FC,RNACentral:URS0000D5DDF4,RNACentral:URS0000D5DE30,RNACentral:URS0000E3FF20,RNACentral:URS0000D5DC30,RNACentral:URS00008B65F0 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,exon,intron,intron,intron,intron,exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879769627 Functional Loss SNV dbSNP153 33..33 33 - - - 41451 RMVar_ID_41451 Human_SNP_ID_152944585 A-to-I Human chr3 + 129201575 129201575 129201575 GTGGTGTGGGTGCTTGTACTCCCAGCTTACTTAGGAGGCCAAGGCAGGAGGATTGCTTGAGCCCA GTGGTGTGGGTGCTTGTACTCCCAGCTTACTTGGGAGGCCAAGGCAGGAGGATTGCTTGAGCCCA A G lnc-COPG1-3,lnc-COPG1-3:2,lnc-COPG1-3:3 RNACentral:URS0000D5DE30,RNACentral:URS0000E3FF20,RNACentral:URS0000D5DE83 lincRNA,lincRNA,lincRNA exon,exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1445677874 Functional Loss SNV dbSNP153 33..33 33 - - - 41452 RMVar_ID_41452 Human_SNP_ID_152960300 A-to-I Human chr3 + 129262370 129262370 129262370 CGCCTCCTGGGTTCACGCCATTCTTCTGCCTCAGCCTCCTGAGTAGCTGAGACTAGAGGCACCCG CGCCTCCTGGGTTCACGCCATTCTTCTGCCTCGGCCTCCTGAGTAGCTGAGACTAGAGGCACCCG A G COPG1 Ensembl:ENSG00000181789 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs897293190 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_221139 41453 RMVar_ID_41453 Human_SNP_ID_152960303 A-to-I Human chr3 + 129262382 129262382 129262382 TCACGCCATTCTTCTGCCTCAGCCTCCTGAGTAGCTGAGACTAGAGGCACCCGCCACCATGCCCA TCACGCCATTCTTCTGCCTCAGCCTCCTGAGTGGCTGAGACTAGAGGCACCCGCCACCATGCCCA A G COPG1 Ensembl:ENSG00000181789 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1429119388 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_221139 41454 RMVar_ID_41454 Human_SNP_ID_152989559 A-to-I Human chr3 - 129377202 129377202 129377202 TGACACTATCCTGGCTAACATGGTGAAACCCCATCTCTACTAAAAATATAAAAAATTAGCTGAGC TGACACTATCCTGGCTAACATGGTGAAACCCCGTCTCTACTAAAAATATAAAAAATTAGCTGAGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1292549357 Functional Loss SNV dbSNP153 33..33 33 - - - 41455 RMVar_ID_41455 Human_SNP_ID_152990848 A-to-I Human chr3 - 129383218 129383218 129383218 TGGAATGCAGTGGCATGATCTCGGCTCACTGTAGCCTCTGTCTCCCTGGTTCAAGCAATTCTGCC TGGAATGCAGTGGCATGATCTCGGCTCACTGTTGCCTCTGTCTCCCTGGTTCAAGCAATTCTGCC T A RPL32P3 Ensembl:ENSG00000251474 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs796809815 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7119553,Human_RBP_ID_14617611,Human_RBP_ID_17406608 41456 RMVar_ID_41456 Human_SNP_ID_152992057 A-to-I Human chr3 - 129387970 129387969 129387971 CATAGCAAGACTCTCTCTCTGCAAAAAAAAAGAAAAAAAAAAAAACCTCCCAAAAAAAAGGTTTT CATAGCAAGACTCTCTCTCTGCAAAAAAAAA__AAAAAAAAAAAACCTCCCAAAAAAAAGGTTTT TTC T RPL32P3 Ensembl:ENSG00000251474 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1295189425 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_18536703 41457 RMVar_ID_41457 Human_SNP_ID_152992059 A-to-I Human chr3 - 129387970 129387970 129387970 CATAGCAAGACTCTCTCTCTGCAAAAAAAAAGAAAAAAAAAAAAACCTCCCAAAAAAAAGGTTTT CATAGCAAGACTCTCTCTCTGCAAAAAAAAAGGAAAAAAAAAAAACCTCCCAAAAAAAAGGTTTT T C RPL32P3 Ensembl:ENSG00000251474 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1159643721 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18536703 41458 RMVar_ID_41458 Human_SNP_ID_153009416 A-to-I Human chr3 + 129455272 129455272 129455272 TCGGCTCATGGCAACCTCTGACTCCCTGGTTCAAGTGATTCTCCTGCCTCAGCCTCCTGAGTAGC TCGGCTCATGGCAACCTCTGACTCCCTGGTTCCAGTGATTCTCCTGCCTCAGCCTCCTGAGTAGC A C IFT122 Ensembl:ENSG00000163913 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251354997 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_30960,RMVar_hsa_circ_45281,RMVar_hsa_circ_375287,RMVar_hsa_circ_265286,RMVar_hsa_circ_221158,RMVar_hsa_circ_264983 41459 RMVar_ID_41459 Human_SNP_ID_153037633 A-to-I Human chr3 - 129560403 129560403 129560403 GGTGCTGCCTACGGACGAGCTGGCGGAGCCCAAGAAGTCTCACCGGCAGAGCCATCGCAAGAAGG GGTGCTGCCTACGGACGAGCTGGCGGAGCCCAGGAAGTCTCACCGGCAGAGCCATCGCAAGAAGG T C PLXND1 Ensembl:ENSG00000004399 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs752712168 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19012998,Human_RBP_ID_22551793,Human_RBP_ID_22677351,Human_RBP_ID_22769411 Human_Splice_Rec_481754,Human_Splice_Rec_481755,Human_Splice_Rec_481790,Human_Splice_Rec_481791,Human_Splice_Rec_481804,Human_Splice_Rec_481805,Human_Splice_Rec_481814,Human_Splice_Rec_481815,Human_Splice_Rec_481819 Human_miRNA_ID_2394614 RMVar_hsa_circ_375982,RMVar_hsa_circ_93019,RMVar_hsa_circ_221169,RMVar_hsa_circ_83585,RMVar_hsa_circ_221170,RMVar_hsa_circ_100208,RMVar_hsa_circ_221172,RMVar_hsa_circ_221173 41460 RMVar_ID_41460 Human_SNP_ID_153077362 A-to-I Human chr3 - 129719978 129719978 129719978 AGGGTCTCACCATGTTGCTGAGGCTTGGTCTCAAACTCCTGGGCTCAAGTGATCCTCCTGCCTTT AGGGTCTCACCATGTTGCTGAGGCTTGGTCTCGAACTCCTGGGCTCAAGTGATCCTCCTGCCTTT T C TMCC1 Ensembl:ENSG00000172765 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1199867058 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26369,RMVar_hsa_circ_78816,RMVar_hsa_circ_127768,RMVar_hsa_circ_221193,RMVar_hsa_circ_221194,RMVar_hsa_circ_364437,RMVar_hsa_circ_221197,RMVar_hsa_circ_363219 41461 RMVar_ID_41461 Human_SNP_ID_153083910 A-to-I Human chr3 - 129748831 129748831 129748831 GCCCAGCTAATTTTTGTAGTTTTAGTAGAGACAGTGTTTTGCCACGTTGGCCAGGCTGGTCTTCA GCCCAGCTAATTTTTGTAGTTTTAGTAGAGACCGTGTTTTGCCACGTTGGCCAGGCTGGTCTTCA T G TMCC1 Ensembl:ENSG00000172765 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1395098285 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26369,RMVar_hsa_circ_78816,RMVar_hsa_circ_127768,RMVar_hsa_circ_221193,RMVar_hsa_circ_221194,RMVar_hsa_circ_364437,RMVar_hsa_circ_221197,RMVar_hsa_circ_363219 41462 RMVar_ID_41462 Human_SNP_ID_153087234 A-to-I Human chr3 - 129761788 129761788 129761788 TGGGGTTTCACCACGTTGGCGAGGCTGCTCTCAAACTCCTGACCTCAGATGATCCGCCTGCCTCA TGGGGTTTCACCACGTTGGCGAGGCTGCTCTCCAACTCCTGACCTCAGATGATCCGCCTGCCTCA T G TMCC1 Ensembl:ENSG00000172765 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934914116 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26369,RMVar_hsa_circ_78816,RMVar_hsa_circ_127768,RMVar_hsa_circ_221193,RMVar_hsa_circ_221194,RMVar_hsa_circ_364437,RMVar_hsa_circ_221197,RMVar_hsa_circ_363219 41463 RMVar_ID_41463 Human_SNP_ID_153088813 A-to-I Human chr3 - 129767096 129767096 129767096 CCATTATGCCCTGCTAATCTTTGTATTTTTGTAGAGACAGGGTTTCACCTTGTTGGGCAGTCTGT CCATTATGCCCTGCTAATCTTTGTATTTTTGTTGAGACAGGGTTTCACCTTGTTGGGCAGTCTGT T A TMCC1 Ensembl:ENSG00000172765 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1340986510 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26369,RMVar_hsa_circ_78816,RMVar_hsa_circ_127768,RMVar_hsa_circ_221193,RMVar_hsa_circ_221194,RMVar_hsa_circ_364437,RMVar_hsa_circ_221197,RMVar_hsa_circ_363219 41464 RMVar_ID_41464 Human_SNP_ID_153088814 A-to-I Human chr3 - 129767096 129767096 129767096 CCATTATGCCCTGCTAATCTTTGTATTTTTGTAGAGACAGGGTTTCACCTTGTTGGGCAGTCTGT CCATTATGCCCTGCTAATCTTTGTATTTTTGTGGAGACAGGGTTTCACCTTGTTGGGCAGTCTGT T C TMCC1 Ensembl:ENSG00000172765 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1340986510 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26369,RMVar_hsa_circ_78816,RMVar_hsa_circ_127768,RMVar_hsa_circ_221193,RMVar_hsa_circ_221194,RMVar_hsa_circ_364437,RMVar_hsa_circ_221197,RMVar_hsa_circ_363219 41465 RMVar_ID_41465 Human_SNP_ID_153092856 A-to-I Human chr3 - 129784842 129784842 129784842 GATCTCCCTCAGCCTCTCAAGTAGCTGGGACTACAGGCATGCACCACCATGCCTGGCTAATTTTG GATCTCCCTCAGCCTCTCAAGTAGCTGGGACTGCAGGCATGCACCACCATGCCTGGCTAATTTTG T C TMCC1 Ensembl:ENSG00000172765 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs912674082 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26369,RMVar_hsa_circ_78816,RMVar_hsa_circ_127768,RMVar_hsa_circ_221193,RMVar_hsa_circ_221194,RMVar_hsa_circ_364437,RMVar_hsa_circ_221197,RMVar_hsa_circ_363219,RMVar_hsa_circ_221201 41466 RMVar_ID_41466 Human_SNP_ID_153097635 A-to-I Human chr3 - 129805300 129805300 129805300 ACAATAGCCAGGCGTGGTGGCCTGTGCCCACAATCTCAGCTACTTGGGAGGCTGAAGTGGGAGGA ACAATAGCCAGGCGTGGTGGCCTGTGCCCACAGTCTCAGCTACTTGGGAGGCTGAAGTGGGAGGA T C TMCC1 Ensembl:ENSG00000172765 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1409863084 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17573835 RMVar_hsa_circ_26369,RMVar_hsa_circ_78816,RMVar_hsa_circ_127768,RMVar_hsa_circ_221193,RMVar_hsa_circ_221194,RMVar_hsa_circ_364437,RMVar_hsa_circ_221204,RMVar_hsa_circ_221197,RMVar_hsa_circ_363219,RMVar_hsa_circ_221201,RMVar_hsa_circ_221205,RMVar_hsa_circ_221203 41467 RMVar_ID_41467 Human_SNP_ID_153176927 A-to-I Human chr3 - 130101633 130101633 130101633 ATCTCACCACTGCACTCCAGCGTGGGCAACAAAGCAAGACCCTGTCTCAAAAAAGCAAAAAAGCA ATCTCACCACTGCACTCCAGCGTGGGCAACAATGCAAGACCCTGTCTCAAAAAAGCAAAAAAGCA T A FAM86HP Ensembl:ENSG00000253540 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1179961534 Functional Loss SNV dbSNP153 33..33 33 - - - 41468 RMVar_ID_41468 Human_SNP_ID_153179236 A-to-I Human chr3 - 130108266 130108256 130108266 AACCCAGCACAAGGCTGGGTGCACTGGTTCACACCTGTAATCCCAGGACATTGGGAGGCTGAGGT AACCCAGCACAAGGCTGGGTGCACTGGTTCAC__________CCAGGACATTGGGAGGCTGAGGT GGATTACAGGT G FAM86HP Ensembl:ENSG00000253540 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1360422560 Functional Loss DEL dbSNP153 33..42 33 - - - Human_RBP_ID_17406204 41469 RMVar_ID_41469 Human_SNP_ID_153365567 A-to-I Human chr3 + 130871764 130871764 130871764 AATCTTTAGGCCAGGGGCGGTGGCTCACCCCTATAATCCCAAACTTTGGGAGGCAGAGGCCGGCG AATCTTTAGGCCAGGGGCGGTGGCTCACCCCTGTAATCCCAAACTTTGGGAGGCAGAGGCCGGCG A G ATP2C1 Ensembl:ENSG00000017260 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1311119202 Functional Loss SNV dbSNP153 33..33 33 - - - 41470 RMVar_ID_41470 Human_SNP_ID_153376851 A-to-I Human chr3 + 130919493 130919493 130919493 CGCCTGCCTCAGCCTCCCAAAGTGCTAGGATTACAGGCATGAGCTACCACGCCCGGCCTAGAGTT CGCCTGCCTCAGCCTCCCAAAGTGCTAGGATTGCAGGCATGAGCTACCACGCCCGGCCTAGAGTT A G ATP2C1 Ensembl:ENSG00000017260 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1559922967 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49384,RMVar_hsa_circ_334299,RMVar_hsa_circ_40798 41471 RMVar_ID_41471 Human_SNP_ID_153387137 A-to-I Human chr3 - 130962870 130962870 130962870 TGGTTGATTTTAAAGTTGAAAGCACATAAGCAACAACATTATTGGCTAAACAATACACACTGAAG TGGTTGATTTTAAAGTTGAAAGCACATAAGCATCAACATTATTGGCTAAACAATACACACTGAAG T A - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs560703629 Functional Loss SNV dbSNP153 33..33 33 - - - 41472 RMVar_ID_41472 Human_SNP_ID_153387138 A-to-I Human chr3 - 130962871 130962871 130962871 CTGGTTGATTTTAAAGTTGAAAGCACATAAGCAACAACATTATTGGCTAAACAATACACACTGAA CTGGTTGATTTTAAAGTTGAAAGCACATAAGCTACAACATTATTGGCTAAACAATACACACTGAA T A - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs529821216 Functional Loss SNV dbSNP153 33..33 33 - - - 41473 RMVar_ID_41473 Human_SNP_ID_153506813 A-to-I Human chr3 - 131478944 131478944 131478944 TCACACCTGTAATCCCAGCACTTTAGGAGGCTAGAGTGGACAGATGACTTGAGGCCAGGAGTTTG TCACACCTGTAATCCCAGCACTTTAGGAGGCTGGAGTGGACAGATGACTTGAGGCCAGGAGTTTG T C MRPL3 Ensembl:ENSG00000114686 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1411964277 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14623374,Human_RBP_ID_25696754 RMVar_hsa_circ_45611,RMVar_hsa_circ_62954,RMVar_hsa_circ_347162 41474 RMVar_ID_41474 Human_SNP_ID_153506820 A-to-I Human chr3 - 131478965 131478965 131478965 TTTTGGGCTGGGCATAGTGGCTCACACCTGTAATCCCAGCACTTTAGGAGGCTAGAGTGGACAGA TTTTGGGCTGGGCATAGTGGCTCACACCTGTACTCCCAGCACTTTAGGAGGCTAGAGTGGACAGA T G MRPL3 Ensembl:ENSG00000114686 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs143425393 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45611,RMVar_hsa_circ_62954,RMVar_hsa_circ_347162 41475 RMVar_ID_41475 Human_SNP_ID_153510428 A-to-I Human chr3 - 131493003 131493003 131493003 TATATTGTGATGAAAGAGGCACTCTTCACATCAGGAAATAAAAAGTGGCATAACTTTTTTGTCAA TATATTGTGATGAAAGAGGCACTCTTCACATCCGGAAATAAAAAGTGGCATAACTTTTTTGTCAA T G MRPL3 Ensembl:ENSG00000114686 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs981178569 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7121595 RMVar_hsa_circ_221299,RMVar_hsa_circ_294900,RMVar_hsa_circ_347162,RMVar_hsa_circ_351888,RMVar_hsa_circ_126135,RMVar_hsa_circ_221298,RMVar_hsa_circ_336790 41476 RMVar_ID_41476 Human_SNP_ID_153677305 A-to-I Human chr3 + 132175673 132175673 132175673 GGCTGCAGATAAGCAGACACTCCAGAGTAAACAACCTTTACAGGTTGCCAGGTGTACAAAGATAA GGCTGCAGATAAGCAGACACTCCAGAGTAAACGACCTTTACAGGTTGCCAGGTGTACAAAGATAA A G PSMC2P1 Ensembl:ENSG00000240854 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1386035905 Functional Loss SNV dbSNP153 33..33 33 - - - 41477 RMVar_ID_41477 Human_SNP_ID_153677318 A-to-I Human chr3 + 132175719 132175719 132175719 GCCAGGTGTACAAAGATAATCAGTGCTGATTCAGAGGACCCAAAATACATTGTCAATGTAAAGCA GCCAGGTGTACAAAGATAATCAGTGCTGATTCGGAGGACCCAAAATACATTGTCAATGTAAAGCA A G PSMC2P1 Ensembl:ENSG00000240854 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878943033 Functional Loss SNV dbSNP153 33..33 33 - - - 41478 RMVar_ID_41478 Human_SNP_ID_153750424 A-to-I Human chr3 + 132485237 132485236 132485238 TTGACCCAATCCAACCTTCGCCTCCCATGTTCAGATGATTCTCTTGGCTCAGCCTCCCGAGTAGC TTGACCCAATCCAACCTTCGCCTCCCATGTTC__ATGATTCTCTTGGCTCAGCCTCCCGAGTAGC CAG C DNAJC13 Ensembl:ENSG00000138246 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879104322 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_107436,RMVar_hsa_circ_103411,RMVar_hsa_circ_221306,RMVar_hsa_circ_63177,RMVar_hsa_circ_221307,RMVar_hsa_circ_124729,RMVar_hsa_circ_221314,RMVar_hsa_circ_221315,RMVar_hsa_circ_95812,RMVar_hsa_circ_221318,RMVar_hsa_circ_70885,RMVar_hsa_circ_83059,RMVar_hsa_circ_221320,RMVar_hsa_circ_40926,RMVar_hsa_circ_24385,RMVar_hsa_circ_65764,RMVar_hsa_circ_50359,RMVar_hsa_circ_63902,RMVar_hsa_circ_78720,RMVar_hsa_circ_221328,RMVar_hsa_circ_12705,RMVar_hsa_circ_221333,RMVar_hsa_circ_72720,RMVar_hsa_circ_221339 41479 RMVar_ID_41479 Human_SNP_ID_153768443 A-to-I Human chr3 - 132561879 132561879 132561879 TATTTACATGACATTCTGGAAAAGGCAAAACTATAGTGATGGAGAACCTATCAATGGTTGCCAGA TATTTACATGACATTCTGGAAAAGGCAAAACTGTAGTGATGGAGAACCTATCAATGGTTGCCAGA T C ACAD11,NPHP3-ACAD11 Ensembl:ENSG00000240303,Ensembl:ENSG00000274810 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1265692426 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120694,RMVar_hsa_circ_68708,RMVar_hsa_circ_221357,RMVar_hsa_circ_77230,RMVar_hsa_circ_221356 41480 RMVar_ID_41480 Human_SNP_ID_153794141 A-to-I Human chr3 + 132674312 132674311 132674312 TTTTATGTGATTTTCTCTGTATAGAAGCTTTTATTATGTTAGTGCAAAGGTAATTGTGGATTTTG TTTTATGTGATTTTCTCTGTATAGAAGCTTTT_TTATGTTAGTGCAAAGGTAATTGTGGATTTTG TA T UBA5 Ensembl:ENSG00000081307 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1559993961 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_8558968,Human_RBP_ID_14625970 RMVar_hsa_circ_22912,RMVar_hsa_circ_60305,RMVar_hsa_circ_72472,RMVar_hsa_circ_42714,RMVar_hsa_circ_70900 41481 RMVar_ID_41481 Human_SNP_ID_153795242 A-to-I Human chr3 + 132679250 132679249 132679251 AGATAGTGCCACTGCACTCCAGTCTGGAAAACAGAGTGAGACTCTGTCTCAAAAAAAAAGGTATT AGATAGTGCCACTGCACTCCAGTCTGGAAAAC__AGTGAGACTCTGTCTCAAAAAAAAAGGTATT CAG C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1390909030 Functional Loss DEL dbSNP153 33..34 33 - - - 41482 RMVar_ID_41482 Human_SNP_ID_153796658 A-to-I Human chr3 - 132685274 132685274 132685274 CTGTCTCTACAAAAAAAATTAATAAATTAGCCAGACATGGTGGTACACACCTGTAGACCCAGCTA CTGTCTCTACAAAAAAAATTAATAAATTAGCCGGACATGGTGGTACACACCTGTAGACCCAGCTA T C NPHP3-ACAD11,NPHP3 Ensembl:ENSG00000274810,Ensembl:ENSG00000113971 Protein coding,Protein coding intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1134175 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29838,RMVar_hsa_circ_279978,RMVar_hsa_circ_325727,RMVar_hsa_circ_357043,RMVar_hsa_circ_345030,RMVar_hsa_circ_74470,RMVar_hsa_circ_53448,RMVar_hsa_circ_221375,RMVar_hsa_circ_12275,RMVar_hsa_circ_221374,RMVar_hsa_circ_365400,RMVar_hsa_circ_371412,RMVar_hsa_circ_100532,RMVar_hsa_circ_106529,RMVar_hsa_circ_221376,RMVar_hsa_circ_221377,RMVar_hsa_circ_268608,RMVar_hsa_circ_356208,RMVar_hsa_circ_221378 41483 RMVar_ID_41483 Human_SNP_ID_153802447 A-to-I Human chr3 - 132708726 132708726 132708726 AAATTAAAGGCATTAAAAAGAACTCCTGGAAAAGCAGTGCAGGAGCCTGGCTGTTGCCCTGGATG AAATTAAAGGCATTAAAAAGAACTCCTGGAAAGGCAGTGCAGGAGCCTGGCTGTTGCCCTGGATG T C NPHP3-ACAD11,NPHP3 Ensembl:ENSG00000274810,Ensembl:ENSG00000113971 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1050884238 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3981,RMVar_hsa_circ_325727,RMVar_hsa_circ_345030,RMVar_hsa_circ_365400,RMVar_hsa_circ_69933,RMVar_hsa_circ_285117,RMVar_hsa_circ_221379,RMVar_hsa_circ_1651,RMVar_hsa_circ_54918,RMVar_hsa_circ_71075,RMVar_hsa_circ_294178,RMVar_hsa_circ_58021,RMVar_hsa_circ_340181,RMVar_hsa_circ_5686,RMVar_hsa_circ_90407,RMVar_hsa_circ_328147,RMVar_hsa_circ_360787,RMVar_hsa_circ_277247,RMVar_hsa_circ_221384,RMVar_hsa_circ_56686,RMVar_hsa_circ_378552,RMVar_hsa_circ_306483,RMVar_hsa_circ_221385 41484 RMVar_ID_41484 Human_SNP_ID_153927330 A-to-I Human chr3 + 133226802 133226802 133226802 ATACTGGAAGTGTATTAGTTTGTTTTCACACTACTAATAAAGACATACCCGCGACTGGGAAATTT ATACTGGAAGTGTATTAGTTTGTTTTCACACTGCTAATAAAGACATACCCGCGACTGGGAAATTT A G TMEM108 Ensembl:ENSG00000144868 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs543719754 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6057,RMVar_hsa_circ_221398,RMVar_hsa_circ_221397 41485 RMVar_ID_41485 Human_SNP_ID_153927333 A-to-I Human chr3 + 133226805 133226805 133226805 CTGGAAGTGTATTAGTTTGTTTTCACACTACTAATAAAGACATACCCGCGACTGGGAAATTTACA CTGGAAGTGTATTAGTTTGTTTTCACACTACTGATAAAGACATACCCGCGACTGGGAAATTTACA A G TMEM108 Ensembl:ENSG00000144868 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1022190201 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6057,RMVar_hsa_circ_221398,RMVar_hsa_circ_221397 41486 RMVar_ID_41486 Human_SNP_ID_154014124 A-to-I Human chr3 + 133580608 133580608 133580608 CCTGTAATCCCAGTTACTTGGTGGGCTGAGATAGAAGAATTGCTTGAACCCGGGAGGCAGAGGTT CCTGTAATCCCAGTTACTTGGTGGGCTGAGATGGAAGAATTGCTTGAACCCGGGAGGCAGAGGTT A G CDV3 Ensembl:ENSG00000091527 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs368423763 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14626860 RMVar_hsa_circ_113168,RMVar_hsa_circ_69172,RMVar_hsa_circ_221402,RMVar_hsa_circ_349222 41487 RMVar_ID_41487 Human_SNP_ID_154020845 A-to-I Human chr3 - 133606125 133606125 133606125 GGAGTGCAGTGGCGTGATCTTGGCTTACTGCAACCTCTGCCTCCCAGGCCCAGGAGATCCACCTC GGAGTGCAGTGGCGTGATCTTGGCTTACTGCATCCTCTGCCTCCCAGGCCCAGGAGATCCACCTC T A TOPBP1 Ensembl:ENSG00000163781 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1338673895 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14627427,Human_RBP_ID_25697285 41488 RMVar_ID_41488 Human_SNP_ID_154023033 A-to-I Human chr3 - 133615471 133615471 133615471 TTGGTGGGGTTTTTTTGTTTTTGTTTTGAGACAGAGTCTTGCTCTGTCTCCCAGGCTTGAGTGCC TTGGTGGGGTTTTTTTGTTTTTGTTTTGAGACGGAGTCTTGCTCTGTCTCCCAGGCTTGAGTGCC T C TOPBP1 Ensembl:ENSG00000163781 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1387986650 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_221410 41489 RMVar_ID_41489 Human_SNP_ID_154023238 A-to-I Human chr3 - 133616274 133616274 133616274 CTACTAAAAATACAAAAAAATTTGCGAGACGTAGAGGCACATGCCTGTGATCCTAGTTACTCAGG CTACTAAAAATACAAAAAAATTTGCGAGACGTGGAGGCACATGCCTGTGATCCTAGTTACTCAGG T C TOPBP1 Ensembl:ENSG00000163781 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs949431603 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14627554 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_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_221410 41490 RMVar_ID_41490 Human_SNP_ID_154025407 A-to-I Human chr3 - 133625107 133625107 133625107 CAAAAATTAGCTGGGTGTGGTGGCGTACGCCTATAATCCCAGCTGCTCAGGAGGCTGAGATAGGA CAAAAATTAGCTGGGTGTGGTGGCGTACGCCTGTAATCCCAGCTGCTCAGGAGGCTGAGATAGGA T C TOPBP1 Ensembl:ENSG00000163781 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs541015116 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_327111,RMVar_hsa_circ_347661,RMVar_hsa_circ_355820,RMVar_hsa_circ_221408,RMVar_hsa_circ_126215,RMVar_hsa_circ_221409,RMVar_hsa_circ_266588,RMVar_hsa_circ_356538,RMVar_hsa_circ_345819,RMVar_hsa_circ_50715,RMVar_hsa_circ_94542,RMVar_hsa_circ_90780,RMVar_hsa_circ_121394,RMVar_hsa_circ_221415,RMVar_hsa_circ_269426,RMVar_hsa_circ_221417,RMVar_hsa_circ_111387,RMVar_hsa_circ_221416,RMVar_hsa_circ_71684,RMVar_hsa_circ_75241,RMVar_hsa_circ_41386,RMVar_hsa_circ_221418,RMVar_hsa_circ_221419,RMVar_hsa_circ_311132,RMVar_hsa_circ_321879,RMVar_hsa_circ_335217,RMVar_hsa_circ_310118,RMVar_hsa_circ_69525,RMVar_hsa_circ_300581,RMVar_hsa_circ_45292,RMVar_hsa_circ_221421,RMVar_hsa_circ_221422,RMVar_hsa_circ_221423,RMVar_hsa_circ_265522,RMVar_hsa_circ_7745,RMVar_hsa_circ_48297 41491 RMVar_ID_41491 Human_SNP_ID_154025452 A-to-I Human chr3 - 133625246 133625246 133625246 GAATATTGAATAGCGGCCGGGCACGGTGGCTCATGCGTGTAATCCCAGCACTTTGGGAGCGCAAG GAATATTGAATAGCGGCCGGGCACGGTGGCTCGTGCGTGTAATCCCAGCACTTTGGGAGCGCAAG T C TOPBP1 Ensembl:ENSG00000163781 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1267398840 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_327111,RMVar_hsa_circ_347661,RMVar_hsa_circ_355820,RMVar_hsa_circ_221408,RMVar_hsa_circ_126215,RMVar_hsa_circ_221409,RMVar_hsa_circ_266588,RMVar_hsa_circ_356538,RMVar_hsa_circ_345819,RMVar_hsa_circ_50715,RMVar_hsa_circ_94542,RMVar_hsa_circ_90780,RMVar_hsa_circ_121394,RMVar_hsa_circ_221415,RMVar_hsa_circ_269426,RMVar_hsa_circ_221417,RMVar_hsa_circ_111387,RMVar_hsa_circ_221416,RMVar_hsa_circ_71684,RMVar_hsa_circ_75241,RMVar_hsa_circ_41386,RMVar_hsa_circ_221418,RMVar_hsa_circ_221419,RMVar_hsa_circ_311132,RMVar_hsa_circ_321879,RMVar_hsa_circ_335217,RMVar_hsa_circ_310118,RMVar_hsa_circ_69525,RMVar_hsa_circ_300581,RMVar_hsa_circ_45292,RMVar_hsa_circ_221421,RMVar_hsa_circ_221422,RMVar_hsa_circ_221423,RMVar_hsa_circ_265522,RMVar_hsa_circ_7745,RMVar_hsa_circ_48297 41492 RMVar_ID_41492 Human_SNP_ID_154026064 A-to-I Human chr3 - 133628190 133628190 133628190 ATTTACCACATCTGTTGAAAATAGCCTCTCACATATCAATTCACTCTTATATGTATATAATGTAT ATTTACCACATCTGTTGAAAATAGCCTCTCACTTATCAATTCACTCTTATATGTATATAATGTAT T A TOPBP1 Ensembl:ENSG00000163781 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1550742 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25697442 GWAS_ID_4785,GWAS_ID_4786,GWAS_ID_4787,GWAS_ID_4788,GWAS_ID_4789,GWAS_ID_4790,GWAS_ID_4791,GWAS_ID_4792,GWAS_ID_4793,GWAS_ID_4794,GWAS_ID_4795,GWAS_ID_4796,GWAS_ID_4797,GWAS_ID_4798,GWAS_ID_4799,GWAS_ID_4800,GWAS_ID_4801,GWAS_ID_4802,GWAS_ID_4803,GWAS_ID_4804 RMVar_hsa_circ_327111,RMVar_hsa_circ_347661,RMVar_hsa_circ_355820,RMVar_hsa_circ_221408,RMVar_hsa_circ_126215,RMVar_hsa_circ_221409,RMVar_hsa_circ_266588,RMVar_hsa_circ_356538,RMVar_hsa_circ_345819,RMVar_hsa_circ_50715,RMVar_hsa_circ_94542,RMVar_hsa_circ_90780,RMVar_hsa_circ_121394,RMVar_hsa_circ_221415,RMVar_hsa_circ_269426,RMVar_hsa_circ_221417,RMVar_hsa_circ_111387,RMVar_hsa_circ_221416,RMVar_hsa_circ_71684,RMVar_hsa_circ_75241,RMVar_hsa_circ_41386,RMVar_hsa_circ_221418,RMVar_hsa_circ_221419,RMVar_hsa_circ_311132,RMVar_hsa_circ_321879,RMVar_hsa_circ_335217,RMVar_hsa_circ_310118,RMVar_hsa_circ_69525,RMVar_hsa_circ_300581,RMVar_hsa_circ_45292,RMVar_hsa_circ_221421,RMVar_hsa_circ_221422,RMVar_hsa_circ_221423,RMVar_hsa_circ_265522,RMVar_hsa_circ_7745,RMVar_hsa_circ_48297 41493 RMVar_ID_41493 Human_SNP_ID_154026065 A-to-I Human chr3 - 133628190 133628190 133628190 ATTTACCACATCTGTTGAAAATAGCCTCTCACATATCAATTCACTCTTATATGTATATAATGTAT ATTTACCACATCTGTTGAAAATAGCCTCTCACGTATCAATTCACTCTTATATGTATATAATGTAT T C TOPBP1 Ensembl:ENSG00000163781 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1550742 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25697442 GWAS_ID_4785,GWAS_ID_4786,GWAS_ID_4787,GWAS_ID_4788,GWAS_ID_4789,GWAS_ID_4790,GWAS_ID_4791,GWAS_ID_4792,GWAS_ID_4793,GWAS_ID_4794,GWAS_ID_4795,GWAS_ID_4796,GWAS_ID_4797,GWAS_ID_4798,GWAS_ID_4799,GWAS_ID_4800,GWAS_ID_4801,GWAS_ID_4802,GWAS_ID_4803,GWAS_ID_4804 RMVar_hsa_circ_327111,RMVar_hsa_circ_347661,RMVar_hsa_circ_355820,RMVar_hsa_circ_221408,RMVar_hsa_circ_126215,RMVar_hsa_circ_221409,RMVar_hsa_circ_266588,RMVar_hsa_circ_356538,RMVar_hsa_circ_345819,RMVar_hsa_circ_50715,RMVar_hsa_circ_94542,RMVar_hsa_circ_90780,RMVar_hsa_circ_121394,RMVar_hsa_circ_221415,RMVar_hsa_circ_269426,RMVar_hsa_circ_221417,RMVar_hsa_circ_111387,RMVar_hsa_circ_221416,RMVar_hsa_circ_71684,RMVar_hsa_circ_75241,RMVar_hsa_circ_41386,RMVar_hsa_circ_221418,RMVar_hsa_circ_221419,RMVar_hsa_circ_311132,RMVar_hsa_circ_321879,RMVar_hsa_circ_335217,RMVar_hsa_circ_310118,RMVar_hsa_circ_69525,RMVar_hsa_circ_300581,RMVar_hsa_circ_45292,RMVar_hsa_circ_221421,RMVar_hsa_circ_221422,RMVar_hsa_circ_221423,RMVar_hsa_circ_265522,RMVar_hsa_circ_7745,RMVar_hsa_circ_48297 41494 RMVar_ID_41494 Human_SNP_ID_154026702 A-to-I Human chr3 - 133630577 133630577 133630577 CAAAAAAATTACAGCGAGTCACCGTGACTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGC CAAAAAAATTACAGCGAGTCACCGTGACTCACCCCTGTAATCCCAGCACTTTGGGAGGCCAAGGC T G TOPBP1 Ensembl:ENSG00000163781 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1276171888 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_327111,RMVar_hsa_circ_347661,RMVar_hsa_circ_221408,RMVar_hsa_circ_126215,RMVar_hsa_circ_221409,RMVar_hsa_circ_266588,RMVar_hsa_circ_356538,RMVar_hsa_circ_345819,RMVar_hsa_circ_94542,RMVar_hsa_circ_121394,RMVar_hsa_circ_221415,RMVar_hsa_circ_269426,RMVar_hsa_circ_221417,RMVar_hsa_circ_111387,RMVar_hsa_circ_221416,RMVar_hsa_circ_75241,RMVar_hsa_circ_41386,RMVar_hsa_circ_221419,RMVar_hsa_circ_311132,RMVar_hsa_circ_321879,RMVar_hsa_circ_335217,RMVar_hsa_circ_310118,RMVar_hsa_circ_69525,RMVar_hsa_circ_221421,RMVar_hsa_circ_221422,RMVar_hsa_circ_221423,RMVar_hsa_circ_221425,RMVar_hsa_circ_48297,RMVar_hsa_circ_299471,RMVar_hsa_circ_325767,RMVar_hsa_circ_307155,RMVar_hsa_circ_57080,RMVar_hsa_circ_221424 41495 RMVar_ID_41495 Human_SNP_ID_154026705 A-to-I Human chr3 - 133630579 133630579 133630579 AACAAAAAAATTACAGCGAGTCACCGTGACTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAG AACAAAAAAATTACAGCGAGTCACCGTGACTCCCACCTGTAATCCCAGCACTTTGGGAGGCCAAG T G TOPBP1 Ensembl:ENSG00000163781 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1323784572 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_327111,RMVar_hsa_circ_347661,RMVar_hsa_circ_221408,RMVar_hsa_circ_126215,RMVar_hsa_circ_221409,RMVar_hsa_circ_266588,RMVar_hsa_circ_356538,RMVar_hsa_circ_345819,RMVar_hsa_circ_94542,RMVar_hsa_circ_121394,RMVar_hsa_circ_221415,RMVar_hsa_circ_269426,RMVar_hsa_circ_221417,RMVar_hsa_circ_111387,RMVar_hsa_circ_221416,RMVar_hsa_circ_75241,RMVar_hsa_circ_41386,RMVar_hsa_circ_221419,RMVar_hsa_circ_311132,RMVar_hsa_circ_321879,RMVar_hsa_circ_335217,RMVar_hsa_circ_310118,RMVar_hsa_circ_69525,RMVar_hsa_circ_221421,RMVar_hsa_circ_221422,RMVar_hsa_circ_221423,RMVar_hsa_circ_221425,RMVar_hsa_circ_48297,RMVar_hsa_circ_299471,RMVar_hsa_circ_325767,RMVar_hsa_circ_307155,RMVar_hsa_circ_57080,RMVar_hsa_circ_221424 41496 RMVar_ID_41496 Human_SNP_ID_154026806 A-to-I Human chr3 - 133631009 133631009 133631009 AATTGTATTTTTTGGAGAGGTAGAGTCTCACCATGTTGCTCAGGCTGGTCTAGAACTCCTGGGCT AATTGTATTTTTTGGAGAGGTAGAGTCTCACCGTGTTGCTCAGGCTGGTCTAGAACTCCTGGGCT T C TOPBP1 Ensembl:ENSG00000163781 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs779723006 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_327111,RMVar_hsa_circ_347661,RMVar_hsa_circ_221408,RMVar_hsa_circ_126215,RMVar_hsa_circ_221409,RMVar_hsa_circ_266588,RMVar_hsa_circ_356538,RMVar_hsa_circ_345819,RMVar_hsa_circ_94542,RMVar_hsa_circ_121394,RMVar_hsa_circ_221415,RMVar_hsa_circ_269426,RMVar_hsa_circ_221417,RMVar_hsa_circ_111387,RMVar_hsa_circ_221416,RMVar_hsa_circ_75241,RMVar_hsa_circ_41386,RMVar_hsa_circ_221419,RMVar_hsa_circ_311132,RMVar_hsa_circ_321879,RMVar_hsa_circ_335217,RMVar_hsa_circ_310118,RMVar_hsa_circ_69525,RMVar_hsa_circ_221421,RMVar_hsa_circ_221422,RMVar_hsa_circ_221423,RMVar_hsa_circ_221425,RMVar_hsa_circ_48297,RMVar_hsa_circ_299471,RMVar_hsa_circ_325767,RMVar_hsa_circ_307155,RMVar_hsa_circ_57080,RMVar_hsa_circ_221424 41497 RMVar_ID_41497 Human_SNP_ID_154027449 A-to-I Human chr3 - 133633784 133633784 133633784 AGGTTTTGTTTTGTTTTGTTGTGTTTAAGACAAGGTCTCGCTGTGTCGTCCAGGCTGGAGTGTAG AGGTTTTGTTTTGTTTTGTTGTGTTTAAGACACGGTCTCGCTGTGTCGTCCAGGCTGGAGTGTAG T G TOPBP1 Ensembl:ENSG00000163781 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1406180973 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_327111,RMVar_hsa_circ_347661,RMVar_hsa_circ_221408,RMVar_hsa_circ_126215,RMVar_hsa_circ_221409,RMVar_hsa_circ_266588,RMVar_hsa_circ_356538,RMVar_hsa_circ_345819,RMVar_hsa_circ_94542,RMVar_hsa_circ_121394,RMVar_hsa_circ_221415,RMVar_hsa_circ_269426,RMVar_hsa_circ_221417,RMVar_hsa_circ_111387,RMVar_hsa_circ_221416,RMVar_hsa_circ_75241,RMVar_hsa_circ_41386,RMVar_hsa_circ_221419,RMVar_hsa_circ_311132,RMVar_hsa_circ_321879,RMVar_hsa_circ_335217,RMVar_hsa_circ_310118,RMVar_hsa_circ_69525,RMVar_hsa_circ_221421,RMVar_hsa_circ_221422,RMVar_hsa_circ_221423,RMVar_hsa_circ_221425,RMVar_hsa_circ_48297,RMVar_hsa_circ_299471,RMVar_hsa_circ_325767,RMVar_hsa_circ_307155,RMVar_hsa_circ_57080,RMVar_hsa_circ_221424 41498 RMVar_ID_41498 Human_SNP_ID_154027808 A-to-I Human chr3 - 133635391 133635391 133635391 TTAATTAGCTGGGCTTGGTGGAGTGCACCTATAGTCCTAGAACTCAGGAGGGTGAGGCAGCAAGA TTAATTAGCTGGGCTTGGTGGAGTGCACCTATGGTCCTAGAACTCAGGAGGGTGAGGCAGCAAGA T C TOPBP1 Ensembl:ENSG00000163781 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1401406061 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7122877,Human_RBP_ID_14627885 RMVar_hsa_circ_327111,RMVar_hsa_circ_347661,RMVar_hsa_circ_221408,RMVar_hsa_circ_126215,RMVar_hsa_circ_221409,RMVar_hsa_circ_266588,RMVar_hsa_circ_356538,RMVar_hsa_circ_345819,RMVar_hsa_circ_94542,RMVar_hsa_circ_121394,RMVar_hsa_circ_221415,RMVar_hsa_circ_269426,RMVar_hsa_circ_221417,RMVar_hsa_circ_111387,RMVar_hsa_circ_221416,RMVar_hsa_circ_75241,RMVar_hsa_circ_41386,RMVar_hsa_circ_221419,RMVar_hsa_circ_311132,RMVar_hsa_circ_321879,RMVar_hsa_circ_335217,RMVar_hsa_circ_310118,RMVar_hsa_circ_69525,RMVar_hsa_circ_221421,RMVar_hsa_circ_221422,RMVar_hsa_circ_221423,RMVar_hsa_circ_221425,RMVar_hsa_circ_48297,RMVar_hsa_circ_299471,RMVar_hsa_circ_325767,RMVar_hsa_circ_307155,RMVar_hsa_circ_57080,RMVar_hsa_circ_221424 41499 RMVar_ID_41499 Human_SNP_ID_154031438 A-to-I Human chr3 - 133651021 133651021 133651021 GTGATCTCAGCTCACTGCAACATCTTCCTCTTAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTA GTGATCTCAGCTCACTGCAACATCTTCCTCTTGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTA T C TOPBP1 Ensembl:ENSG00000163781 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs943597613 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126215,RMVar_hsa_circ_221409,RMVar_hsa_circ_94542,RMVar_hsa_circ_121394,RMVar_hsa_circ_221415,RMVar_hsa_circ_221417,RMVar_hsa_circ_221419,RMVar_hsa_circ_311132,RMVar_hsa_circ_35306,RMVar_hsa_circ_48297,RMVar_hsa_circ_57080,RMVar_hsa_circ_57138,RMVar_hsa_circ_50809,RMVar_hsa_circ_265280,RMVar_hsa_circ_221428,RMVar_hsa_circ_221429,RMVar_hsa_circ_276219 41500 RMVar_ID_41500 Human_SNP_ID_154031730 A-to-I Human chr3 - 133652020 133652020 133652020 GCATCAGCCACCCCTCAGTCTCCCGAGCAGTTAGAACTACAGGCATGTGCCACTACACCTGGCTA GCATCAGCCACCCCTCAGTCTCCCGAGCAGTTGGAACTACAGGCATGTGCCACTACACCTGGCTA T C TOPBP1 Ensembl:ENSG00000163781 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1216953421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7123005,Human_RBP_ID_14628217 RMVar_hsa_circ_126215,RMVar_hsa_circ_221409,RMVar_hsa_circ_94542,RMVar_hsa_circ_121394,RMVar_hsa_circ_221415,RMVar_hsa_circ_221417,RMVar_hsa_circ_221419,RMVar_hsa_circ_311132,RMVar_hsa_circ_35306,RMVar_hsa_circ_48297,RMVar_hsa_circ_57080,RMVar_hsa_circ_57138,RMVar_hsa_circ_50809,RMVar_hsa_circ_265280,RMVar_hsa_circ_221428,RMVar_hsa_circ_221429,RMVar_hsa_circ_276219 41501 RMVar_ID_41501 Human_SNP_ID_154032165 A-to-I Human chr3 - 133653794 133653794 133653794 AACCCCGTGTCTACTAAAAATACAAAAAAATTAGCCAGACATGGTGGCACACGTCTGTAATCCTA AACCCCGTGTCTACTAAAAATACAAAAAAATTGGCCAGACATGGTGGCACACGTCTGTAATCCTA T C TOPBP1 Ensembl:ENSG00000163781 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1322019891 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126215,RMVar_hsa_circ_221409,RMVar_hsa_circ_94542,RMVar_hsa_circ_121394,RMVar_hsa_circ_221415,RMVar_hsa_circ_221417,RMVar_hsa_circ_57138,RMVar_hsa_circ_265280,RMVar_hsa_circ_68788,RMVar_hsa_circ_221428,RMVar_hsa_circ_62552,RMVar_hsa_circ_85996,RMVar_hsa_circ_106540,RMVar_hsa_circ_369333,RMVar_hsa_circ_96456,RMVar_hsa_circ_221432,RMVar_hsa_circ_221433,RMVar_hsa_circ_221434,RMVar_hsa_circ_221431 41502 RMVar_ID_41502 Human_SNP_ID_154032451 A-to-I Human chr3 - 133655041 133655041 133655041 CCACCACGCCTGAATAACTTTTTATTTTTAGTAGAGACGGGCTTTCACCATGTTGGCCAGACTGG CCACCACGCCTGAATAACTTTTTATTTTTAGTGGAGACGGGCTTTCACCATGTTGGCCAGACTGG T C TOPBP1 Ensembl:ENSG00000163781 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1036996648 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14628284,Human_RBP_ID_25697685 RMVar_hsa_circ_126215,RMVar_hsa_circ_221409,RMVar_hsa_circ_94542,RMVar_hsa_circ_121394,RMVar_hsa_circ_221415,RMVar_hsa_circ_221417,RMVar_hsa_circ_57138,RMVar_hsa_circ_265280,RMVar_hsa_circ_68788,RMVar_hsa_circ_221428,RMVar_hsa_circ_62552,RMVar_hsa_circ_85996,RMVar_hsa_circ_106540,RMVar_hsa_circ_369333,RMVar_hsa_circ_96456,RMVar_hsa_circ_221432,RMVar_hsa_circ_221433,RMVar_hsa_circ_221434,RMVar_hsa_circ_221431 41503 RMVar_ID_41503 Human_SNP_ID_154162276 A-to-I Human chr3 - 134195690 134195671 134195690 TGTCCGCCTTGGCCTCCCAAAGTGTTGGGATTACAGGCGTGAGCCACCGCACCTGGCCAATACTC TGTCCGCCTTGGCCTCCCAAAGTGTTGGGATT___________________CCTGGCCAATACTC GTGCGGTGGCTCACGCCTGT G RYK Ensembl:ENSG00000163785 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1374858450 Functional Loss DEL dbSNP153 33..51 33 - - - RMVar_hsa_circ_637,RMVar_hsa_circ_265661,RMVar_hsa_circ_349397,RMVar_hsa_circ_299615,RMVar_hsa_circ_274272,RMVar_hsa_circ_17879,RMVar_hsa_circ_221473,RMVar_hsa_circ_221474,RMVar_hsa_circ_221472,RMVar_hsa_circ_310934,RMVar_hsa_circ_345586,RMVar_hsa_circ_349926,RMVar_hsa_circ_19680,RMVar_hsa_circ_221484,RMVar_hsa_circ_221485,RMVar_hsa_circ_289321,RMVar_hsa_circ_353795,RMVar_hsa_circ_221487,RMVar_hsa_circ_17865,RMVar_hsa_circ_332460,RMVar_hsa_circ_8886 41504 RMVar_ID_41504 Human_SNP_ID_553446543 A-to-I Human chr14 + 45098304 45098304 45098304 CTTGTCTCAAAAACAAAAAACATTAGCTGGGCATGGTGGCGCATGCCTGTAGTTCTAGCTACTCG CTTGTCTCAAAAACAAAAAACATTAGCTGGGCCTGGTGGCGCATGCCTGTAGTTCTAGCTACTCG A C PRPF39 Ensembl:ENSG00000185246 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs941641590 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38208,RMVar_hsa_circ_54316,RMVar_hsa_circ_344632,RMVar_hsa_circ_370180,RMVar_hsa_circ_340050,RMVar_hsa_circ_54756,RMVar_hsa_circ_60640,RMVar_hsa_circ_166221,RMVar_hsa_circ_166222,RMVar_hsa_circ_64957 41505 RMVar_ID_41505 Human_SNP_ID_553446988 A-to-I Human chr14 + 45100123 45100123 45100123 ATGCTGGCAGGAGTCTGTAATCCCAGCTTCTCAGGAGGCTGAGGTAGGAGAATTGCTTGAACCTG ATGCTGGCAGGAGTCTGTAATCCCAGCTTCTCGGGAGGCTGAGGTAGGAGAATTGCTTGAACCTG A G PRPF39 Ensembl:ENSG00000185246 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs541456365 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38208,RMVar_hsa_circ_54316,RMVar_hsa_circ_344632,RMVar_hsa_circ_370180,RMVar_hsa_circ_340050,RMVar_hsa_circ_54756,RMVar_hsa_circ_60640,RMVar_hsa_circ_166221,RMVar_hsa_circ_166222,RMVar_hsa_circ_64957 41506 RMVar_ID_41506 Human_SNP_ID_553451096 A-to-I Human chr14 - 45116769 45116769 45116769 TTGCTGCAACCTCTGCCTCCCGGGCTCAAGCAATTCTCCTGCCTCACCCTCCCTGGTAGCTGGAA TTGCTGCAACCTCTGCCTCCCGGGCTCAAGCAGTTCTCCTGCCTCACCCTCCCTGGTAGCTGGAA T C FKBP3 Ensembl:ENSG00000100442 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167536374 Functional Loss SNV dbSNP153 33..33 33 - - - 41507 RMVar_ID_41507 Human_SNP_ID_553451115 A-to-I Human chr14 - 45116850 45116848 45116850 TAGCATATTTTGTTTTGGTTTTTTTTTGAGACAGGGTCTCGCTCTGTCACCCAGGCTGGAGTGCA TAGCATATTTTGTTTTGGTTTTTTTTTGAGAC__GGTCTCGCTCTGTCACCCAGGCTGGAGTGCA CCT C FKBP3 Ensembl:ENSG00000100442 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1302104057 Functional Loss DEL dbSNP153 33..34 33 - - - 41508 RMVar_ID_41508 Human_SNP_ID_553451596 A-to-I Human chr14 - 45118447 45118447 45118447 TTTTTATTTTTAGTAGAAGATGGGGTTTCACTATGTTAGCTAGGCTGGTCTCAAACTCCTGACCT TTTTTATTTTTAGTAGAAGATGGGGTTTCACTGTGTTAGCTAGGCTGGTCTCAAACTCCTGACCT T C FKBP3 Ensembl:ENSG00000100442 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1316473100 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_31554,RMVar_hsa_circ_341926,RMVar_hsa_circ_166230,RMVar_hsa_circ_166231 41509 RMVar_ID_41509 Human_SNP_ID_553451851 A-to-I Human chr14 - 45119457 45119457 45119457 TCAAGCGATTCTCCTGCCTCAGCCTCCCGAATAGCTGGGATTACAGGCATGCGCCACCACACCTA TCAAGCGATTCTCCTGCCTCAGCCTCCCGAATCGCTGGGATTACAGGCATGCGCCACCACACCTA T G FKBP3 Ensembl:ENSG00000100442 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs946788155 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_31554,RMVar_hsa_circ_341926,RMVar_hsa_circ_166230,RMVar_hsa_circ_166231 41510 RMVar_ID_41510 Human_SNP_ID_553451874 A-to-I Human chr14 - 45119522 45119522 45119522 TCTTGTTGTCCAGGCTGGAGTACAATGGTGCAATCTCGGCTTACTGCAACCTCTGTCTCCTGAGT TCTTGTTGTCCAGGCTGGAGTACAATGGTGCAGTCTCGGCTTACTGCAACCTCTGTCTCCTGAGT T C FKBP3 Ensembl:ENSG00000100442 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1281721421 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_31554,RMVar_hsa_circ_341926,RMVar_hsa_circ_166230,RMVar_hsa_circ_166231 41511 RMVar_ID_41511 Human_SNP_ID_553452020 A-to-I Human chr14 - 45119971 45119971 45119971 TTGTTACCTGCCCCAGCCAGGCGTGGTGGCTCATGCCTGTAATTGCAGCAATTTGGGAGGCCGAG TTGTTACCTGCCCCAGCCAGGCGTGGTGGCTCGTGCCTGTAATTGCAGCAATTTGGGAGGCCGAG T C FKBP3 Ensembl:ENSG00000100442 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs148559310 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_31554,RMVar_hsa_circ_341926,RMVar_hsa_circ_166230,RMVar_hsa_circ_166231 41512 RMVar_ID_41512 Human_SNP_ID_553452737 A-to-I Human chr14 - 45122967 45122967 45122967 GCTGATCTCAAACTCTTGACCTCAAGTGATCCACCCACCTTGGCCTCCCAAAGTGCTGAGATTAC GCTGATCTCAAACTCTTGACCTCAAGTGATCCTCCCACCTTGGCCTCCCAAAGTGCTGAGATTAC T A FKBP3 Ensembl:ENSG00000100442 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs990020470 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_341926,RMVar_hsa_circ_166230,RMVar_hsa_circ_166231,RMVar_hsa_circ_302555,RMVar_hsa_circ_166232 41513 RMVar_ID_41513 Human_SNP_ID_553452746 A-to-I Human chr14 - 45123010 45123010 45123010 TTTTGTATTTTTAATAGAGATGGGGTTTTACCATGTTGGCCAGGCTGATCTCAAACTCTTGACCT TTTTGTATTTTTAATAGAGATGGGGTTTTACCGTGTTGGCCAGGCTGATCTCAAACTCTTGACCT T C FKBP3 Ensembl:ENSG00000100442 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1303346881 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_341926,RMVar_hsa_circ_166230,RMVar_hsa_circ_166231,RMVar_hsa_circ_302555,RMVar_hsa_circ_166232 41514 RMVar_ID_41514 Human_SNP_ID_553452756 A-to-I Human chr14 - 45123065 45123065 45123065 ACTCTACCTCCCGAGTAGCTGGGATTACAGGCACACGCCACCACATCCACCTAATTTTTGTATTT ACTCTACCTCCCGAGTAGCTGGGATTACAGGCGCACGCCACCACATCCACCTAATTTTTGTATTT T C FKBP3 Ensembl:ENSG00000100442 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs928498987 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_341926,RMVar_hsa_circ_166230,RMVar_hsa_circ_166231,RMVar_hsa_circ_302555,RMVar_hsa_circ_166232 41515 RMVar_ID_41515 Human_SNP_ID_553453146 A-to-I Human chr14 - 45124449 45124449 45124449 TGGCTCACTGCAACCTCTGCCTCCTGGATTCAAGTGATTCTCCTGCTTCAGCCCCCTAAATAGCT TGGCTCACTGCAACCTCTGCCTCCTGGATTCAGGTGATTCTCCTGCTTCAGCCCCCTAAATAGCT T C FKBP3 Ensembl:ENSG00000100442 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs954379968 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_341926,RMVar_hsa_circ_166230,RMVar_hsa_circ_166231,RMVar_hsa_circ_302555,RMVar_hsa_circ_166232 41516 RMVar_ID_41516 Human_SNP_ID_553454848 A-to-I Human chr14 - 45131591 45131591 45131591 AGAGTCTTGCTCTGTCACCTAGGCTGGAATGCAGTGGTGCGATCTCGGCTCACTGCAACCTCCAC AGAGTCTTGCTCTGTCACCTAGGCTGGAATGCGGTGGTGCGATCTCGGCTCACTGCAACCTCCAC T C FKBP3 Ensembl:ENSG00000100442 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs759773244 Functional Loss SNV dbSNP153 33..33 33 - - - 41517 RMVar_ID_41517 Human_SNP_ID_553455084 A-to-I Human chr14 - 45132465 45132465 45132465 TCAACCCAAGAGGGGGAGGTTGCAGTGGGCCGAGATTGGGCCACTGCACTCCAGCCTGGGCGACA TCAACCCAAGAGGGGGAGGTTGCAGTGGGCCGCGATTGGGCCACTGCACTCCAGCCTGGGCGACA T G FKBP3 Ensembl:ENSG00000100442 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1370098664 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22711677 41518 RMVar_ID_41518 Human_SNP_ID_553455094 A-to-I Human chr14 - 45132487 45132487 45132487 AGGCTGAGGCAGGAGAATCGTTTCAACCCAAGAGGGGGAGGTTGCAGTGGGCCGAGATTGGGCCA AGGCTGAGGCAGGAGAATCGTTTCAACCCAAGGGGGGGAGGTTGCAGTGGGCCGAGATTGGGCCA T C FKBP3 Ensembl:ENSG00000100442 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs988082093 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12332755,Human_RBP_ID_22711677 41519 RMVar_ID_41519 Human_SNP_ID_553455115 A-to-I Human chr14 - 45132562 45132562 45132562 ACCTCATTTCTACTAAAAATACAAAAAAAATTAGCTGGGCCTGGTGGTGGGCGCCTCTAATCCCA ACCTCATTTCTACTAAAAATACAAAAAAAATTGGCTGGGCCTGGTGGTGGGCGCCTCTAATCCCA T C FKBP3 Ensembl:ENSG00000100442 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1447609827 Functional Loss SNV dbSNP153 33..33 33 - - - 41520 RMVar_ID_41520 Human_SNP_ID_553455122 A-to-I Human chr14 - 45132594 45132594 45132594 GCATTGAGGACCAGCCTGGCCAACGTAGCGAAACCTCATTTCTACTAAAAATACAAAAAAAATTA GCATTGAGGACCAGCCTGGCCAACGTAGCGAATCCTCATTTCTACTAAAAATACAAAAAAAATTA T A FKBP3 Ensembl:ENSG00000100442 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1231254838 Functional Loss SNV dbSNP153 33..33 33 - - - 41521 RMVar_ID_41521 Human_SNP_ID_553455149 A-to-I Human chr14 - 45132664 45132664 45132664 TTCGGAGGCCAAAGCGGGCGGATCACGAGGTCAGGAGATCGAGACCATCCTGACTAACAGTTGAG TTCGGAGGCCAAAGCGGGCGGATCACGAGGTCGGGAGATCGAGACCATCCTGACTAACAGTTGAG T C FKBP3 Ensembl:ENSG00000100442 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1426137189 Functional Loss SNV dbSNP153 33..33 33 - - - 41522 RMVar_ID_41522 Human_SNP_ID_553457806 A-to-I Human chr14 + 45141689 45141689 45141689 TTGGCTCACTGCAACCTCCGCCTCCTGGATTCAAGCGATTCTCTTGCCTCACCCTCCCGAGTAGC TTGGCTCACTGCAACCTCCGCCTCCTGGATTCGAGCGATTCTCTTGCCTCACCCTCCCGAGTAGC A G FANCM Ensembl:ENSG00000187790 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1566723042 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14910,RMVar_hsa_circ_61109 41523 RMVar_ID_41523 Human_SNP_ID_553464491 A-to-I Human chr14 + 45166398 45166398 45166398 GGACCTCGTGATCTGCCCGCCTGGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCAC GGACCTCGTGATCTGCCCGCCTGGGCCTCCCAGAGTGCTGGGATTACAGGCGTGAGCCACCGCAC A G FANCM Ensembl:ENSG00000187790 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1415840958 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24114,RMVar_hsa_circ_61109,RMVar_hsa_circ_38566,RMVar_hsa_circ_275574,RMVar_hsa_circ_28434,RMVar_hsa_circ_30929,RMVar_hsa_circ_24168,RMVar_hsa_circ_166234,RMVar_hsa_circ_166235,RMVar_hsa_circ_68722,RMVar_hsa_circ_166233,RMVar_hsa_circ_345963,RMVar_hsa_circ_13177,RMVar_hsa_circ_51144 41524 RMVar_ID_41524 Human_SNP_ID_553465522 A-to-I Human chr14 + 45170465 45170465 45170465 GGAGGATTGCTTGAACCCAGGAGTTTGAGGTTACAGTGAGTTATGAATGTGCTGTTGCACTCCAA GGAGGATTGCTTGAACCCAGGAGTTTGAGGTTTCAGTGAGTTATGAATGTGCTGTTGCACTCCAA A T FANCM Ensembl:ENSG00000187790 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167708027 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24114,RMVar_hsa_circ_61109,RMVar_hsa_circ_38566,RMVar_hsa_circ_275574,RMVar_hsa_circ_30929,RMVar_hsa_circ_24168,RMVar_hsa_circ_166234,RMVar_hsa_circ_166235,RMVar_hsa_circ_68722,RMVar_hsa_circ_166233,RMVar_hsa_circ_345963,RMVar_hsa_circ_13177,RMVar_hsa_circ_51144 41525 RMVar_ID_41525 Human_SNP_ID_553469343 A-to-I Human chr14 + 45184835 45184835 45184835 GCTGTTACTGCCACAGACTGGAGTGCAGTGGCACCATCTCAGCTCACTGCAACCTTCACCTCCCA GCTGTTACTGCCACAGACTGGAGTGCAGTGGCGCCATCTCAGCTCACTGCAACCTTCACCTCCCA A G FANCM Ensembl:ENSG00000187790 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1466579817 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38566,RMVar_hsa_circ_30929,RMVar_hsa_circ_166233,RMVar_hsa_circ_71840,RMVar_hsa_circ_51144,RMVar_hsa_circ_360529,RMVar_hsa_circ_338277,RMVar_hsa_circ_57050,RMVar_hsa_circ_347055,RMVar_hsa_circ_364115 41526 RMVar_ID_41526 Human_SNP_ID_553469344 A-to-I Human chr14 + 45184843 45184843 45184843 TGCCACAGACTGGAGTGCAGTGGCACCATCTCAGCTCACTGCAACCTTCACCTCCCAGGTTCAAG TGCCACAGACTGGAGTGCAGTGGCACCATCTCCGCTCACTGCAACCTTCACCTCCCAGGTTCAAG A C FANCM Ensembl:ENSG00000187790 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1426456711 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38566,RMVar_hsa_circ_30929,RMVar_hsa_circ_166233,RMVar_hsa_circ_71840,RMVar_hsa_circ_51144,RMVar_hsa_circ_360529,RMVar_hsa_circ_338277,RMVar_hsa_circ_57050,RMVar_hsa_circ_347055,RMVar_hsa_circ_364115 41527 RMVar_ID_41527 Human_SNP_ID_553475065 A-to-I Human chr14 - 45207594 45207594 45207594 CAGGTTGGAGAGCAGTGGCACAATCTCGGCTCACTACCGCCTCCATCTACCAGGTTCAAGCAATT CAGGTTGGAGAGCAGTGGCACAATCTCGGCTCTCTACCGCCTCCATCTACCAGGTTCAAGCAATT T A MIS18BP1 Ensembl:ENSG00000129534 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs376080599 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19116,RMVar_hsa_circ_61339,RMVar_hsa_circ_62493,RMVar_hsa_circ_30722 41528 RMVar_ID_41528 Human_SNP_ID_553478172 A-to-I Human chr14 - 45220222 45220222 45220222 TGTGGGGTATGTGCCTGTAGTGCCAACCACTAAGGAGGCGGAGTCAGGGGGATCGCCTGAGCCCA TGTGGGGTATGTGCCTGTAGTGCCAACCACTATGGAGGCGGAGTCAGGGGGATCGCCTGAGCCCA T A MIS18BP1 Ensembl:ENSG00000129534 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs529762679 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23622928 RMVar_hsa_circ_61339,RMVar_hsa_circ_62493,RMVar_hsa_circ_30722,RMVar_hsa_circ_166245,RMVar_hsa_circ_335164,RMVar_hsa_circ_344822,RMVar_hsa_circ_345457,RMVar_hsa_circ_330936,RMVar_hsa_circ_54329,RMVar_hsa_circ_166244 41529 RMVar_ID_41529 Human_SNP_ID_553485653 A-to-I Human chr14 - 45249331 45249331 45249331 CTGTAATCCCAGCACTTTGGGAGGCTGAGGCAAGTGGATCACCTGAGGTCAGGAGACCAGCCTGA CTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGTGGATCACCTGAGGTCAGGAGACCAGCCTGA T C MIS18BP1 Ensembl:ENSG00000129534 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs554024097 Functional Loss SNV dbSNP153 33..33 33 - - - 41530 RMVar_ID_41530 Human_SNP_ID_554114464 A-to-I Human chr14 - 47649641 47649640 47649641 TCACTCTGTTGCCCAGGCTGGAGGGCAATGGCATGATGTCGGTTTACTATAACCTCTGCCTCCCA TCACTCTGTTGCCCAGGCTGGAGGGCAATGGC_TGATGTCGGTTTACTATAACCTCTGCCTCCCA AT A MDGA2 Ensembl:ENSG00000139915 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1287119393 Functional Loss DEL dbSNP153 33..33 33 - - - 41531 RMVar_ID_41531 Human_SNP_ID_554318739 A-to-I Human chr14 - 48407996 48407996 48407996 GATTGTAAGTTTCCTGAGGCCTCCCCAGTCATATAGAACTGTGATTTAATTAAACTTCCTTTCTT GATTGTAAGTTTCCTGAGGCCTCCCCAGTCATTTAGAACTGTGATTTAATTAAACTTCCTTTCTT T A AL358335.2 Ensembl:ENSG00000258751 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006687171 Functional Loss SNV dbSNP153 33..33 33 - - - 41532 RMVar_ID_41532 Human_SNP_ID_554617210 A-to-I Human chr14 - 49572182 49572182 49572182 ACATTGGGAGGCCAAGGCAGGTGGATCACCTGAGGTTAGGAGTTCGAGAGCAGCCTGGCCAACAC ACATTGGGAGGCCAAGGCAGGTGGATCACCTGGGGTTAGGAGTTCGAGAGCAGCCTGGCCAACAC T C RPS29 Ensembl:ENSG00000213741 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1468692710 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114563,RMVar_hsa_circ_166277 41533 RMVar_ID_41533 Human_SNP_ID_554617354 A-to-I Human chr14 - 49572818 49572818 49572818 GAGATCCACCTGCCTTGGCCTCCCAAAATGCTAGGACTGCAGGCGTGAGCCACCATGCCAGGCCA GAGATCCACCTGCCTTGGCCTCCCAAAATGCTGGGACTGCAGGCGTGAGCCACCATGCCAGGCCA T C RPS29 Ensembl:ENSG00000213741 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1394209144 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6407817,Human_RBP_ID_12337480 RMVar_hsa_circ_114563,RMVar_hsa_circ_166277 41534 RMVar_ID_41534 Human_SNP_ID_554618160 A-to-I Human chr14 - 49575831 49575831 49575831 TATTTTAATTTTTTTGGACATGGCCTTGCTCTATCACCCAGACTGGCATTCAGTGGCACAAACAT TATTTTAATTTTTTTGGACATGGCCTTGCTCTGTCACCCAGACTGGCATTCAGTGGCACAAACAT T C RPS29 Ensembl:ENSG00000213741 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs927139278 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_446202,Human_RBP_ID_6351258,Human_RBP_ID_12337612,Human_RBP_ID_17848762,Human_RBP_ID_23623558 RMVar_hsa_circ_114563,RMVar_hsa_circ_166277 41535 RMVar_ID_41535 Human_SNP_ID_554620638 A-to-I Human chr14 - 49584058 49584058 49584058 AGAATCGCTTGAACCCAGGAGGCTGAGGTTGCAGTGAGTGGAGATGGCTCCATTGCACTCCAGTC AGAATCGCTTGAACCCAGGAGGCTGAGGTTGCGGTGAGTGGAGATGGCTCCATTGCACTCCAGTC T C RPS29 Ensembl:ENSG00000213741 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971359686 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_231406,Human_RBP_ID_17562544 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 41536 RMVar_ID_41536 Human_SNP_ID_554620693 A-to-I Human chr14 - 49584256 49584254 49584256 CTAGATGAACTGGGCCAGGCGAGGTGCCTCACACCTGAAATCCCAGCACTTTGGGAGGCCGACAA CTAGATGAACTGGGCCAGGCGAGGTGCCTCAC__CTGAAATCCCAGCACTTTGGGAGGCCGACAA GGT G RPS29 Ensembl:ENSG00000213741 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs768444879 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_22797912 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 41537 RMVar_ID_41537 Human_SNP_ID_554620868 A-to-I Human chr14 - 49584759 49584759 49584759 TATAATGATGTAAATTTTTTTTTTTGTTTTGAAATTGGGTCTCCCTCTGTTTCCCAGGCTGGAGT TATAATGATGTAAATTTTTTTTTTTGTTTTGACATTGGGTCTCCCTCTGTTTCCCAGGCTGGAGT T G RPS29 Ensembl:ENSG00000213741 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1566480965 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12337947 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 41538 RMVar_ID_41538 Human_SNP_ID_554621053 A-to-I Human chr14 - 49585205 49585205 49585205 TGCCACCATGTCCGGCTAATTTTTTTATTTTTAGTAGAGACGGGGTTTTACCATGTTGGTCAGGC TGCCACCATGTCCGGCTAATTTTTTTATTTTTGGTAGAGACGGGGTTTTACCATGTTGGTCAGGC T C RPS29 Ensembl:ENSG00000213741 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs528986366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12337969 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 41539 RMVar_ID_41539 Human_SNP_ID_554624124 A-to-I Human chr14 - 49595368 49595368 49595368 TTGCCTAGTCTGGTCTTGAACTCCTGACCTCAAGCTGTCCTCCTGCCTCAGCCTCCCAAAGTGCT TTGCCTAGTCTGGTCTTGAACTCCTGACCTCAGGCTGTCCTCCTGCCTCAGCCTCCCAAAGTGCT T C RPS29 Ensembl:ENSG00000213741 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1475724722 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 41540 RMVar_ID_41540 Human_SNP_ID_554624125 A-to-I Human chr14 - 49595369 49595369 49595369 GTTGCCTAGTCTGGTCTTGAACTCCTGACCTCAAGCTGTCCTCCTGCCTCAGCCTCCCAAAGTGC GTTGCCTAGTCTGGTCTTGAACTCCTGACCTCGAGCTGTCCTCCTGCCTCAGCCTCCCAAAGTGC T C RPS29 Ensembl:ENSG00000213741 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs996090150 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 41541 RMVar_ID_41541 Human_SNP_ID_554625655 A-to-I Human chr14 + 49600208 49600208 49600208 CTATAACACCGCCGGACAGGAAGACTATGACCATCTGAGGCCTTTATCTTACCCAATGACCGACG CTATAACACCGCCGGACAGGAAGACTATGACCGTCTGAGGCCTTTATCTTACCCAATGACCGACG A G RHOQP1,LRR1 Ensembl:ENSG00000258568,Ensembl:ENSG00000165501 Pseudogene,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1229755366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1494109,Human_RBP_ID_5564090,Human_RBP_ID_17249259,Human_RBP_ID_18528625,Human_RBP_ID_27431332 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 41542 RMVar_ID_41542 Human_SNP_ID_554626963 A-to-I Human chr14 + 49604244 49604244 49604244 GGAGGATCACTTGAGCCTGGGAGGTGCAGGTTACAATGAGCCAAGATTGCACCACTGCACTCCAA GGAGGATCACTTGAGCCTGGGAGGTGCAGGTTGCAATGAGCCAAGATTGCACCACTGCACTCCAA A G LRR1 Ensembl:ENSG00000165501 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1315042688 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23306816 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,RMVar_hsa_circ_166298,RMVar_hsa_circ_287372 41543 RMVar_ID_41543 Human_SNP_ID_554627013 A-to-I Human chr14 + 49604442 49604442 49604442 AACCTGGAGGCCAGACACGGTGGCTCACGCCTATGATCCCAGCACTTTGGGAGCCCTAGTTGGGC AACCTGGAGGCCAGACACGGTGGCTCACGCCTGTGATCCCAGCACTTTGGGAGCCCTAGTTGGGC A G LRR1 Ensembl:ENSG00000165501 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs934335836 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1942921,Human_miRNA_ID_1945965,Human_miRNA_ID_2086603,Human_miRNA_ID_2117112,Human_miRNA_ID_2200691,Human_miRNA_ID_2203754,Human_miRNA_ID_2316231,Human_miRNA_ID_2319386,Human_miRNA_ID_2322544,Human_miRNA_ID_2325715,Human_miRNA_ID_2328829,Human_miRNA_ID_2520093,Human_miRNA_ID_2523256,Human_miRNA_ID_2775098,Human_miRNA_ID_2816213,Human_miRNA_ID_2822454,Human_miRNA_ID_2828580,Human_miRNA_ID_2831737,Human_miRNA_ID_2835857,Human_miRNA_ID_2841212,Human_miRNA_ID_2846336,Human_miRNA_ID_2849357,Human_miRNA_ID_2863476,Human_miRNA_ID_3113207 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,RMVar_hsa_circ_166298,RMVar_hsa_circ_287372 41544 RMVar_ID_41544 Human_SNP_ID_554627127 A-to-I Human chr14 + 49604921 49604921 49604921 CAACCTTGCTTTTTTTTTCTTTTTGATGAGACAAGGTCTCACTCTCACCTAGGCTGGAGTGCAGT CAACCTTGCTTTTTTTTTCTTTTTGATGAGACGAGGTCTCACTCTCACCTAGGCTGGAGTGCAGT A G LRR1 Ensembl:ENSG00000165501 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1345977758 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12338142,Human_RBP_ID_22923761 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,RMVar_hsa_circ_166298,RMVar_hsa_circ_287372 41545 RMVar_ID_41545 Human_SNP_ID_554627151 A-to-I Human chr14 + 49605035 49605035 49605035 CTTCCTTCTCAGCCTCCCAAGTAACTGGGACTATAGGGGCACAACACCATACCAGGCTAATTTTT CTTCCTTCTCAGCCTCCCAAGTAACTGGGACTGTAGGGGCACAACACCATACCAGGCTAATTTTT A G LRR1 Ensembl:ENSG00000165501 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs114316312 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,RMVar_hsa_circ_166298,RMVar_hsa_circ_287372 41546 RMVar_ID_41546 Human_SNP_ID_554627488 A-to-I Human chr14 + 49606295 49606295 49606295 GTGATCCACCCACCTTGGCCTCCCAAAGTGCTAGGATTATAGGCGTGAGCCACCAGTCCCAGCCT GTGATCCACCCACCTTGGCCTCCCAAAGTGCTGGGATTATAGGCGTGAGCCACCAGTCCCAGCCT A G LRR1 Ensembl:ENSG00000165501 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1358951657 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,RMVar_hsa_circ_166298,RMVar_hsa_circ_287372 41547 RMVar_ID_41547 Human_SNP_ID_554629030 A-to-I Human chr14 + 49611199 49611199 49611199 AACCTGAGAAACATTTAAAACATCTGAAGGCCAGGTGCGGTGGCTCACGCCTGTAACCCCAGCAC AACCTGAGAAACATTTAAAACATCTGAAGGCCTGGTGCGGTGGCTCACGCCTGTAACCCCAGCAC A T LRR1 Ensembl:ENSG00000165501 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1238810964 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,RMVar_hsa_circ_105416,RMVar_hsa_circ_166300 41548 RMVar_ID_41548 Human_SNP_ID_554629202 A-to-I Human chr14 + 49611736 49611736 49611736 CTTGAGGCCAGGAGTTTGAGACCAGCAGGGCTAATATGGTGAAACCCTGTCTCCACTAAAAATAC CTTGAGGCCAGGAGTTTGAGACCAGCAGGGCTCATATGGTGAAACCCTGTCTCCACTAAAAATAC A C LRR1 Ensembl:ENSG00000165501 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1298207568 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,RMVar_hsa_circ_105416,RMVar_hsa_circ_166300 41549 RMVar_ID_41549 Human_SNP_ID_554629203 A-to-I Human chr14 + 49611736 49611736 49611736 CTTGAGGCCAGGAGTTTGAGACCAGCAGGGCTAATATGGTGAAACCCTGTCTCCACTAAAAATAC CTTGAGGCCAGGAGTTTGAGACCAGCAGGGCTGATATGGTGAAACCCTGTCTCCACTAAAAATAC A G LRR1 Ensembl:ENSG00000165501 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1298207568 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,RMVar_hsa_circ_105416,RMVar_hsa_circ_166300 41550 RMVar_ID_41550 Human_SNP_ID_554633822 A-to-I Human chr14 - 49626642 49626642 49626642 AAAATTAGCCGGGCGTGGTGGTGCATGCCTGTAATCCCCTCTACTTGGGAGGCTGAGGCAGAATT AAAATTAGCCGGGCGTGGTGGTGCATGCCTGTCATCCCCTCTACTTGGGAGGCTGAGGCAGAATT T G DNAAF2 Ensembl:ENSG00000165506 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1285154093 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 41551 RMVar_ID_41551 Human_SNP_ID_554634138 A-to-I Human chr14 - 49627755 49627755 49627755 CGCCTCCTGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGAGCATG CGCCTCCTGGGTTCAAGCGATTCTCCTGCCTCGGCCTCCCAAGTAGCTGGGACTACAGGAGCATG T C DNAAF2 Ensembl:ENSG00000165506 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs928198172 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 41552 RMVar_ID_41552 Human_SNP_ID_554634501 A-to-I Human chr14 - 49629065 49629065 49629065 CCAGCTACTGTAGAGGCTGAGGCGGGAGGATCACTTGAGCCTGGGAGGTCAAGGCTGCAGCGAGC CCAGCTACTGTAGAGGCTGAGGCGGGAGGATCGCTTGAGCCTGGGAGGTCAAGGCTGCAGCGAGC T C DNAAF2 Ensembl:ENSG00000165506 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1484526515 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 41553 RMVar_ID_41553 Human_SNP_ID_554634778 A-to-I Human chr14 - 49630163 49630163 49630163 GCAGTGGTGCGATCATGGCTCACTGCAGCCTCAACCTCCCAGACTCAAGCGATCATCCCACCTTA GCAGTGGTGCGATCATGGCTCACTGCAGCCTCGACCTCCCAGACTCAAGCGATCATCCCACCTTA T C DNAAF2 Ensembl:ENSG00000165506 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1566509779 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 41554 RMVar_ID_41554 Human_SNP_ID_554635248 A-to-I Human chr14 - 49631501 49631501 49631501 CCTGCCTCAGCCTCCCGAGTAGCTGGGCCTACAGGCACCTGCCACCACGCCAGGCTAATTTTTTG CCTGCCTCAGCCTCCCGAGTAGCTGGGCCTACGGGCACCTGCCACCACGCCAGGCTAATTTTTTG T C DNAAF2 Ensembl:ENSG00000165506 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs370536273 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 41555 RMVar_ID_41555 Human_SNP_ID_554639052 A-to-I Human chr14 + 49643147 49643146 49643148 CACATATTTTTATTTCTTTCTCTTTTTTTGACAGAGTCTCGCTCTGTCACCCAGGCTGGAGTACA CACATATTTTTATTTCTTTCTCTTTTTTTGAC__AGTCTCGCTCTGTCACCCAGGCTGGAGTACA CAG C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1231093755 Functional Loss DEL dbSNP153 33..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 41556 RMVar_ID_41556 Human_SNP_ID_554639053 A-to-I Human chr14 + 49643147 49643147 49643147 CACATATTTTTATTTCTTTCTCTTTTTTTGACAGAGTCTCGCTCTGTCACCCAGGCTGGAGTACA CACATATTTTTATTTCTTTCTCTTTTTTTGACTGAGTCTCGCTCTGTCACCCAGGCTGGAGTACA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1302802044 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 41557 RMVar_ID_41557 Human_SNP_ID_554639567 A-to-I Human chr14 + 49644891 49644891 49644891 GGTGAAACTCCATCTCTACTAAAAATACAAAAAATCAGCCAGGCGTGGTGGCATGTGCCTGTGAT GGTGAAACTCCATCTCTACTAAAAATACAAAAGATCAGCCAGGCGTGGTGGCATGTGCCTGTGAT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947304121 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 41558 RMVar_ID_41558 Human_SNP_ID_554639761 A-to-I Human chr14 + 49645639 49645639 49645639 AGAGTGAGCATCAACTGCAAGTACCATGAGACAGGGTACTTGACAGCTGTCACCCAGGCTGGAGT AGAGTGAGCATCAACTGCAAGTACCATGAGACCGGGTACTTGACAGCTGTCACCCAGGCTGGAGT A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1190086986 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 41559 RMVar_ID_41559 Human_SNP_ID_554640063 A-to-I Human chr14 - 49646516 49646516 49646516 GAGTTTGAGACCAGCCTGACCAACATGGTGAAACCCCGTCTTTATTAAAAATACAAAAATTACCC GAGTTTGAGACCAGCCTGACCAACATGGTGAACCCCCGTCTTTATTAAAAATACAAAAATTACCC T G POLE2 Ensembl:ENSG00000100479 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs992152106 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 41560 RMVar_ID_41560 Human_SNP_ID_554642890 A-to-I Human chr14 - 49657031 49657031 49657031 TCGGCTTACTACAACCTCCATCTCCTAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGC TCGGCTTACTACAACCTCCATCTCCTAGGTTCTAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGC T A POLE2 Ensembl:ENSG00000100479 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1252333465 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,RMVar_hsa_circ_98339,RMVar_hsa_circ_278249,RMVar_hsa_circ_99492,RMVar_hsa_circ_166304,RMVar_hsa_circ_166305,RMVar_hsa_circ_166306,RMVar_hsa_circ_166308,RMVar_hsa_circ_301823,RMVar_hsa_circ_359645,RMVar_hsa_circ_320659,RMVar_hsa_circ_324695,RMVar_hsa_circ_375779,RMVar_hsa_circ_316926,RMVar_hsa_circ_267591,RMVar_hsa_circ_166307 41561 RMVar_ID_41561 Human_SNP_ID_554643047 A-to-I Human chr14 - 49657578 49657578 49657578 AAATTGGCTGGATGCGGTGGCATGTGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAA AAATTGGCTGGATGCGGTGGCATGTGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAA T C POLE2 Ensembl:ENSG00000100479 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1484592515 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,RMVar_hsa_circ_98339,RMVar_hsa_circ_278249,RMVar_hsa_circ_99492,RMVar_hsa_circ_166304,RMVar_hsa_circ_166305,RMVar_hsa_circ_166306,RMVar_hsa_circ_166308,RMVar_hsa_circ_301823,RMVar_hsa_circ_359645,RMVar_hsa_circ_320659,RMVar_hsa_circ_324695,RMVar_hsa_circ_375779,RMVar_hsa_circ_316926,RMVar_hsa_circ_267591,RMVar_hsa_circ_166307 41562 RMVar_ID_41562 Human_SNP_ID_554643056 A-to-I Human chr14 - 49657648 49657648 49657648 ATCATTTGAGGTCAGGAGTTCAAGACCAGCCTAGCCAACATGGTGAAACCCCATCTCTACTAAAA ATCATTTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAA T C POLE2 Ensembl:ENSG00000100479 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1566539750 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,RMVar_hsa_circ_98339,RMVar_hsa_circ_278249,RMVar_hsa_circ_99492,RMVar_hsa_circ_166304,RMVar_hsa_circ_166305,RMVar_hsa_circ_166306,RMVar_hsa_circ_166308,RMVar_hsa_circ_301823,RMVar_hsa_circ_359645,RMVar_hsa_circ_320659,RMVar_hsa_circ_324695,RMVar_hsa_circ_375779,RMVar_hsa_circ_316926,RMVar_hsa_circ_267591,RMVar_hsa_circ_166307 41563 RMVar_ID_41563 Human_SNP_ID_554643469 A-to-I Human chr14 - 49659352 49659352 49659352 TTCTTCAGGCTGGAATGCAGTGATATGATTATAGCTCACTGCAACCTCAAATTCCTGGACATAAG TTCTTCAGGCTGGAATGCAGTGATATGATTATTGCTCACTGCAACCTCAAATTCCTGGACATAAG T A POLE2 Ensembl:ENSG00000100479 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1244908300 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19941143 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_98339,RMVar_hsa_circ_278249,RMVar_hsa_circ_99492,RMVar_hsa_circ_166304,RMVar_hsa_circ_166305,RMVar_hsa_circ_166306,RMVar_hsa_circ_166308,RMVar_hsa_circ_301823,RMVar_hsa_circ_359645,RMVar_hsa_circ_320659,RMVar_hsa_circ_324695,RMVar_hsa_circ_375779,RMVar_hsa_circ_316926,RMVar_hsa_circ_267591,RMVar_hsa_circ_166307 41564 RMVar_ID_41564 Human_SNP_ID_554643562 A-to-I Human chr14 - 49659795 49659794 49659795 GTTGCTTAAGGCCAGGAGTTTGAGACCAGTCTAGACAACATAACAAAACCTCATCTCTACCAACA GTTGCTTAAGGCCAGGAGTTTGAGACCAGTCT_GACAACATAACAAAACCTCATCTCTACCAACA CT C POLE2 Ensembl:ENSG00000100479 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1228434392 Functional Loss DEL 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,RMVar_hsa_circ_98339,RMVar_hsa_circ_278249,RMVar_hsa_circ_99492,RMVar_hsa_circ_166304,RMVar_hsa_circ_166305,RMVar_hsa_circ_166306,RMVar_hsa_circ_166308,RMVar_hsa_circ_301823,RMVar_hsa_circ_359645,RMVar_hsa_circ_320659,RMVar_hsa_circ_324695,RMVar_hsa_circ_375779,RMVar_hsa_circ_316926,RMVar_hsa_circ_267591,RMVar_hsa_circ_166307 41565 RMVar_ID_41565 Human_SNP_ID_554643749 A-to-I Human chr14 - 49660709 49660709 49660709 TTTTGTATTTTTAGTAGAGACAGGGTTTCGCTATGTTGGTCAGGCTGGTCTTGAACTCCCGACCT TTTTGTATTTTTAGTAGAGACAGGGTTTCGCTTTGTTGGTCAGGCTGGTCTTGAACTCCCGACCT T A POLE2 Ensembl:ENSG00000100479 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1348629993 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,RMVar_hsa_circ_98339,RMVar_hsa_circ_278249,RMVar_hsa_circ_99492,RMVar_hsa_circ_166304,RMVar_hsa_circ_166305,RMVar_hsa_circ_166306,RMVar_hsa_circ_166308,RMVar_hsa_circ_301823,RMVar_hsa_circ_359645,RMVar_hsa_circ_320659,RMVar_hsa_circ_324695,RMVar_hsa_circ_375779,RMVar_hsa_circ_316926,RMVar_hsa_circ_267591,RMVar_hsa_circ_166307 41566 RMVar_ID_41566 Human_SNP_ID_554643761 A-to-I Human chr14 - 49660779 49660779 49660779 TCAAGTGATTCTCCTGCCTTAGCCTCCCAAGTAGCTGGGATTACAGGCATGTGCCACCACACTCA TCAAGTGATTCTCCTGCCTTAGCCTCCCAAGTTGCTGGGATTACAGGCATGTGCCACCACACTCA T A POLE2 Ensembl:ENSG00000100479 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1241612347 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,RMVar_hsa_circ_98339,RMVar_hsa_circ_278249,RMVar_hsa_circ_99492,RMVar_hsa_circ_166304,RMVar_hsa_circ_166305,RMVar_hsa_circ_166306,RMVar_hsa_circ_166308,RMVar_hsa_circ_301823,RMVar_hsa_circ_359645,RMVar_hsa_circ_320659,RMVar_hsa_circ_324695,RMVar_hsa_circ_375779,RMVar_hsa_circ_316926,RMVar_hsa_circ_267591,RMVar_hsa_circ_166307 41567 RMVar_ID_41567 Human_SNP_ID_554654660 A-to-I Human chr14 + 49700130 49700130 49700130 CTCACTGCAACCTCCGCCTCCCAGGTTCAACCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGG CTCACTGCAACCTCCGCCTCCCAGGTTCAACCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGG A G KLHDC1 Ensembl:ENSG00000197776 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1464829914 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_120661 Human_Splice_Rec_1511546,Human_Splice_Rec_1511547 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 41568 RMVar_ID_41568 Human_SNP_ID_554661891 A-to-I Human chr14 + 49726013 49726013 49726013 GGGACTACAGGCGTGGACCACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGACGGAATTTTG GGGACTACAGGCGTGGACCACCATGCCTGGCTGATTTTTGTATTTTTAGTAGAGACGGAATTTTG A G KLHDC1 Ensembl:ENSG00000197776 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1192282224 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,RMVar_hsa_circ_33352,RMVar_hsa_circ_166323,RMVar_hsa_circ_352190,RMVar_hsa_circ_350221,RMVar_hsa_circ_285052,RMVar_hsa_circ_166325,RMVar_hsa_circ_283540,RMVar_hsa_circ_166324,RMVar_hsa_circ_56160,RMVar_hsa_circ_166327,RMVar_hsa_circ_289242,RMVar_hsa_circ_328089,RMVar_hsa_circ_342412,RMVar_hsa_circ_362229,RMVar_hsa_circ_334396,RMVar_hsa_circ_48577,RMVar_hsa_circ_166329,RMVar_hsa_circ_166330,RMVar_hsa_circ_166328,RMVar_hsa_circ_297902,RMVar_hsa_circ_329178,RMVar_hsa_circ_166326,RMVar_hsa_circ_353212,RMVar_hsa_circ_321407,RMVar_hsa_circ_166333,RMVar_hsa_circ_166334,RMVar_hsa_circ_166332 41569 RMVar_ID_41569 Human_SNP_ID_554674807 A-to-I Human chr14 + 49775739 49775739 49775739 ATCTCCGCCTCCCAGGTTCAAGTGATTCTCGTACCTCAGCCTCCTGAGTAGCTGGGATTACAGGC ATCTCCGCCTCCCAGGTTCAAGTGATTCTCGTCCCTCAGCCTCCTGAGTAGCTGGGATTACAGGC A C KLHDC2 Ensembl:ENSG00000165516 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1313654275 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,RMVar_hsa_circ_30586,RMVar_hsa_circ_61052,RMVar_hsa_circ_76483,RMVar_hsa_circ_123939,RMVar_hsa_circ_166337,RMVar_hsa_circ_166338,RMVar_hsa_circ_337982,RMVar_hsa_circ_350078,RMVar_hsa_circ_103230,RMVar_hsa_circ_7603,RMVar_hsa_circ_56905,RMVar_hsa_circ_74983,RMVar_hsa_circ_166339,RMVar_hsa_circ_166340,RMVar_hsa_circ_350441,RMVar_hsa_circ_33743,RMVar_hsa_circ_166341 41570 RMVar_ID_41570 Human_SNP_ID_554678752 A-to-I Human chr14 - 49788874 49788873 49788874 TAAGGAGAGGCTTTGATTCTGATGGGAACTGAATTAAATTAAGACAGAGAGGCCTGGCACGGTGG TAAGGAGAGGCTTTGATTCTGATGGGAACTGA_TTAAATTAAGACAGAGAGGCCTGGCACGGTGG AT A NEMF Ensembl:ENSG00000165525 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1470799768 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_76409,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_31921,RMVar_hsa_circ_106478,RMVar_hsa_circ_166356,RMVar_hsa_circ_268082,RMVar_hsa_circ_268149 41571 RMVar_ID_41571 Human_SNP_ID_554678753 A-to-I Human chr14 - 49788874 49788874 49788874 TAAGGAGAGGCTTTGATTCTGATGGGAACTGAATTAAATTAAGACAGAGAGGCCTGGCACGGTGG TAAGGAGAGGCTTTGATTCTGATGGGAACTGAGTTAAATTAAGACAGAGAGGCCTGGCACGGTGG T C NEMF Ensembl:ENSG00000165525 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7150226 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76409,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_31921,RMVar_hsa_circ_106478,RMVar_hsa_circ_166356,RMVar_hsa_circ_268082,RMVar_hsa_circ_268149 41572 RMVar_ID_41572 Human_SNP_ID_554682856 A-to-I Human chr14 - 49804210 49804210 49804210 CATGAAGTCAGGAGTTCAAGGCCAGCCTGGCCAATATGGTGAAACCCCGTCTCTACTAAAAAATA CATGAAGTCAGGAGTTCAAGGCCAGCCTGGCCGATATGGTGAAACCCCGTCTCTACTAAAAAATA T C NEMF Ensembl:ENSG00000165525 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1200328189 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76409,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_1277,RMVar_hsa_circ_72774,RMVar_hsa_circ_348040,RMVar_hsa_circ_359769,RMVar_hsa_circ_308326,RMVar_hsa_circ_74853,RMVar_hsa_circ_310361,RMVar_hsa_circ_352570,RMVar_hsa_circ_166357,RMVar_hsa_circ_361376,RMVar_hsa_circ_368230,RMVar_hsa_circ_323169,RMVar_hsa_circ_333912,RMVar_hsa_circ_296132,RMVar_hsa_circ_73505,RMVar_hsa_circ_166362,RMVar_hsa_circ_166363,RMVar_hsa_circ_166364,RMVar_hsa_circ_166361,RMVar_hsa_circ_340756,RMVar_hsa_circ_379010,RMVar_hsa_circ_363389,RMVar_hsa_circ_349111,RMVar_hsa_circ_303566,RMVar_hsa_circ_306001,RMVar_hsa_circ_166366,RMVar_hsa_circ_166367,RMVar_hsa_circ_56359,RMVar_hsa_circ_267621,RMVar_hsa_circ_166371,RMVar_hsa_circ_316624,RMVar_hsa_circ_345075,RMVar_hsa_circ_335453,RMVar_hsa_circ_276455,RMVar_hsa_circ_166372,RMVar_hsa_circ_166373,RMVar_hsa_circ_166370,RMVar_hsa_circ_43596,RMVar_hsa_circ_372451 41573 RMVar_ID_41573 Human_SNP_ID_554682917 A-to-I Human chr14 - 49804504 49804504 49804504 CACCACCACGCCTGGCTAATTTTAGTAGAGACAGGGTTTCACCATCTTAGCCAGGCTGGTCTTGA CACCACCACGCCTGGCTAATTTTAGTAGAGACCGGGTTTCACCATCTTAGCCAGGCTGGTCTTGA T G NEMF Ensembl:ENSG00000165525 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1308046544 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76409,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_1277,RMVar_hsa_circ_72774,RMVar_hsa_circ_348040,RMVar_hsa_circ_359769,RMVar_hsa_circ_308326,RMVar_hsa_circ_74853,RMVar_hsa_circ_310361,RMVar_hsa_circ_352570,RMVar_hsa_circ_166357,RMVar_hsa_circ_361376,RMVar_hsa_circ_368230,RMVar_hsa_circ_323169,RMVar_hsa_circ_333912,RMVar_hsa_circ_296132,RMVar_hsa_circ_73505,RMVar_hsa_circ_166362,RMVar_hsa_circ_166363,RMVar_hsa_circ_166364,RMVar_hsa_circ_166361,RMVar_hsa_circ_340756,RMVar_hsa_circ_379010,RMVar_hsa_circ_363389,RMVar_hsa_circ_349111,RMVar_hsa_circ_303566,RMVar_hsa_circ_306001,RMVar_hsa_circ_166366,RMVar_hsa_circ_166367,RMVar_hsa_circ_56359,RMVar_hsa_circ_267621,RMVar_hsa_circ_166371,RMVar_hsa_circ_316624,RMVar_hsa_circ_345075,RMVar_hsa_circ_335453,RMVar_hsa_circ_276455,RMVar_hsa_circ_166372,RMVar_hsa_circ_166373,RMVar_hsa_circ_166370,RMVar_hsa_circ_43596,RMVar_hsa_circ_372451 41574 RMVar_ID_41574 Human_SNP_ID_554684740 A-to-I Human chr14 - 49810794 49810794 49810794 TAGAGATGAGGTTTTGCCATGTTGTCCAGACTAGTGTCGAGCTCCTGAGCTCGAGCAGTCCATCC TAGAGATGAGGTTTTGCCATGTTGTCCAGACTGGTGTCGAGCTCCTGAGCTCGAGCAGTCCATCC T C NEMF Ensembl:ENSG00000165525 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs926519998 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12339422 RMVar_hsa_circ_76409,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_1277,RMVar_hsa_circ_348040,RMVar_hsa_circ_359769,RMVar_hsa_circ_308326,RMVar_hsa_circ_74853,RMVar_hsa_circ_310361,RMVar_hsa_circ_166357,RMVar_hsa_circ_361376,RMVar_hsa_circ_368230,RMVar_hsa_circ_323169,RMVar_hsa_circ_333912,RMVar_hsa_circ_296132,RMVar_hsa_circ_73505,RMVar_hsa_circ_166362,RMVar_hsa_circ_166363,RMVar_hsa_circ_166364,RMVar_hsa_circ_166361,RMVar_hsa_circ_379010,RMVar_hsa_circ_363389,RMVar_hsa_circ_349111,RMVar_hsa_circ_303566,RMVar_hsa_circ_306001,RMVar_hsa_circ_166366,RMVar_hsa_circ_166367,RMVar_hsa_circ_56359,RMVar_hsa_circ_267621,RMVar_hsa_circ_28810,RMVar_hsa_circ_166371,RMVar_hsa_circ_316624,RMVar_hsa_circ_345075,RMVar_hsa_circ_335453,RMVar_hsa_circ_166372,RMVar_hsa_circ_166373,RMVar_hsa_circ_43596,RMVar_hsa_circ_372451,RMVar_hsa_circ_323871,RMVar_hsa_circ_350826,RMVar_hsa_circ_360485,RMVar_hsa_circ_330309,RMVar_hsa_circ_166374,RMVar_hsa_circ_23477,RMVar_hsa_circ_23820,RMVar_hsa_circ_166376,RMVar_hsa_circ_166377,RMVar_hsa_circ_166375 41575 RMVar_ID_41575 Human_SNP_ID_554686000 A-to-I Human chr14 - 49815852 49815852 49815852 TCACCCCATTCTTTTGCCTTAGCCTCCCGAGTAGGTGAGACTACAGGCGCCTGTCACCACACCCG TCACCCCATTCTTTTGCCTTAGCCTCCCGAGTGGGTGAGACTACAGGCGCCTGTCACCACACCCG T C NEMF Ensembl:ENSG00000165525 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1369843846 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76409,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_1277,RMVar_hsa_circ_359769,RMVar_hsa_circ_308326,RMVar_hsa_circ_74853,RMVar_hsa_circ_310361,RMVar_hsa_circ_166357,RMVar_hsa_circ_368230,RMVar_hsa_circ_323169,RMVar_hsa_circ_333912,RMVar_hsa_circ_296132,RMVar_hsa_circ_73505,RMVar_hsa_circ_10183,RMVar_hsa_circ_166362,RMVar_hsa_circ_166363,RMVar_hsa_circ_166364,RMVar_hsa_circ_379010,RMVar_hsa_circ_349111,RMVar_hsa_circ_303566,RMVar_hsa_circ_306001,RMVar_hsa_circ_166366,RMVar_hsa_circ_166367,RMVar_hsa_circ_28810,RMVar_hsa_circ_316624,RMVar_hsa_circ_345075,RMVar_hsa_circ_166372,RMVar_hsa_circ_166373,RMVar_hsa_circ_43596,RMVar_hsa_circ_372451,RMVar_hsa_circ_323871,RMVar_hsa_circ_360485,RMVar_hsa_circ_330309,RMVar_hsa_circ_166374,RMVar_hsa_circ_23477,RMVar_hsa_circ_23820,RMVar_hsa_circ_166376,RMVar_hsa_circ_166375,RMVar_hsa_circ_25136,RMVar_hsa_circ_283554,RMVar_hsa_circ_305324,RMVar_hsa_circ_38588,RMVar_hsa_circ_15462,RMVar_hsa_circ_166378,RMVar_hsa_circ_166379,RMVar_hsa_circ_166381,RMVar_hsa_circ_266893,RMVar_hsa_circ_332814,RMVar_hsa_circ_46834,RMVar_hsa_circ_166380 41576 RMVar_ID_41576 Human_SNP_ID_554686011 A-to-I Human chr14 - 49815907 49815896 49815907 TAGGCTGGAGTGCAGGGGTGCCATCTCAGCTCACTGCAAGCTCCGCCTCCCAGGTTCACCCCATT TAGGCTGGAGTGCAGGGGTGCCATCTCAGCTC___________CGCCTCCCAGGTTCACCCCATT GGAGCTTGCAGT G NEMF Ensembl:ENSG00000165525 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1485838271 Functional Loss DEL dbSNP153 33..43 33 - - - RMVar_hsa_circ_76409,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_1277,RMVar_hsa_circ_359769,RMVar_hsa_circ_308326,RMVar_hsa_circ_74853,RMVar_hsa_circ_310361,RMVar_hsa_circ_166357,RMVar_hsa_circ_368230,RMVar_hsa_circ_323169,RMVar_hsa_circ_333912,RMVar_hsa_circ_296132,RMVar_hsa_circ_73505,RMVar_hsa_circ_10183,RMVar_hsa_circ_166362,RMVar_hsa_circ_166363,RMVar_hsa_circ_166364,RMVar_hsa_circ_379010,RMVar_hsa_circ_349111,RMVar_hsa_circ_303566,RMVar_hsa_circ_306001,RMVar_hsa_circ_166366,RMVar_hsa_circ_166367,RMVar_hsa_circ_28810,RMVar_hsa_circ_316624,RMVar_hsa_circ_345075,RMVar_hsa_circ_166372,RMVar_hsa_circ_166373,RMVar_hsa_circ_43596,RMVar_hsa_circ_372451,RMVar_hsa_circ_323871,RMVar_hsa_circ_360485,RMVar_hsa_circ_330309,RMVar_hsa_circ_166374,RMVar_hsa_circ_23477,RMVar_hsa_circ_23820,RMVar_hsa_circ_166376,RMVar_hsa_circ_166375,RMVar_hsa_circ_25136,RMVar_hsa_circ_283554,RMVar_hsa_circ_305324,RMVar_hsa_circ_38588,RMVar_hsa_circ_15462,RMVar_hsa_circ_166378,RMVar_hsa_circ_166379,RMVar_hsa_circ_166381,RMVar_hsa_circ_266893,RMVar_hsa_circ_332814,RMVar_hsa_circ_46834,RMVar_hsa_circ_166380 41577 RMVar_ID_41577 Human_SNP_ID_554686354 A-to-I Human chr14 - 49817393 49817393 49817393 CTCTGTCACCCAGGCTGAAGTGCAGTGGTGCAATCTTGGCTCATTGCAACTTCTGCCTCCTGGGT CTCTGTCACCCAGGCTGAAGTGCAGTGGTGCAGTCTTGGCTCATTGCAACTTCTGCCTCCTGGGT T C NEMF Ensembl:ENSG00000165525 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs540756475 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76409,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_1277,RMVar_hsa_circ_359769,RMVar_hsa_circ_308326,RMVar_hsa_circ_74853,RMVar_hsa_circ_310361,RMVar_hsa_circ_166357,RMVar_hsa_circ_368230,RMVar_hsa_circ_323169,RMVar_hsa_circ_333912,RMVar_hsa_circ_296132,RMVar_hsa_circ_73505,RMVar_hsa_circ_10183,RMVar_hsa_circ_166362,RMVar_hsa_circ_166363,RMVar_hsa_circ_166364,RMVar_hsa_circ_379010,RMVar_hsa_circ_349111,RMVar_hsa_circ_303566,RMVar_hsa_circ_306001,RMVar_hsa_circ_166366,RMVar_hsa_circ_166367,RMVar_hsa_circ_28810,RMVar_hsa_circ_316624,RMVar_hsa_circ_345075,RMVar_hsa_circ_166372,RMVar_hsa_circ_166373,RMVar_hsa_circ_43596,RMVar_hsa_circ_372451,RMVar_hsa_circ_323871,RMVar_hsa_circ_360485,RMVar_hsa_circ_330309,RMVar_hsa_circ_166374,RMVar_hsa_circ_23477,RMVar_hsa_circ_23820,RMVar_hsa_circ_166376,RMVar_hsa_circ_166375,RMVar_hsa_circ_25136,RMVar_hsa_circ_283554,RMVar_hsa_circ_305324,RMVar_hsa_circ_38588,RMVar_hsa_circ_15462,RMVar_hsa_circ_166378,RMVar_hsa_circ_166379,RMVar_hsa_circ_166381,RMVar_hsa_circ_266893,RMVar_hsa_circ_332814,RMVar_hsa_circ_46834,RMVar_hsa_circ_166380 41578 RMVar_ID_41578 Human_SNP_ID_554686841 A-to-I Human chr14 - 49819104 49819103 49819104 GCACCCTCCTTTTCTTTTTTTCTTTTGGAGACAGAGTTTCGCTCTGTGGCACAGGCTGCTGAGTA GCACCCTCCTTTTCTTTTTTTCTTTTGGAGAC_GAGTTTCGCTCTGTGGCACAGGCTGCTGAGTA CT C NEMF Ensembl:ENSG00000165525 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1337678225 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_76409,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_1277,RMVar_hsa_circ_359769,RMVar_hsa_circ_308326,RMVar_hsa_circ_74853,RMVar_hsa_circ_310361,RMVar_hsa_circ_166357,RMVar_hsa_circ_368230,RMVar_hsa_circ_323169,RMVar_hsa_circ_333912,RMVar_hsa_circ_296132,RMVar_hsa_circ_73505,RMVar_hsa_circ_10183,RMVar_hsa_circ_166362,RMVar_hsa_circ_166363,RMVar_hsa_circ_166364,RMVar_hsa_circ_379010,RMVar_hsa_circ_349111,RMVar_hsa_circ_303566,RMVar_hsa_circ_306001,RMVar_hsa_circ_166366,RMVar_hsa_circ_166367,RMVar_hsa_circ_28810,RMVar_hsa_circ_316624,RMVar_hsa_circ_345075,RMVar_hsa_circ_166372,RMVar_hsa_circ_166373,RMVar_hsa_circ_43596,RMVar_hsa_circ_372451,RMVar_hsa_circ_323871,RMVar_hsa_circ_360485,RMVar_hsa_circ_330309,RMVar_hsa_circ_166374,RMVar_hsa_circ_23477,RMVar_hsa_circ_23820,RMVar_hsa_circ_166376,RMVar_hsa_circ_166375,RMVar_hsa_circ_25136,RMVar_hsa_circ_283554,RMVar_hsa_circ_305324,RMVar_hsa_circ_38588,RMVar_hsa_circ_15462,RMVar_hsa_circ_166378,RMVar_hsa_circ_166379,RMVar_hsa_circ_166381,RMVar_hsa_circ_266893,RMVar_hsa_circ_332814,RMVar_hsa_circ_46834,RMVar_hsa_circ_166380 41579 RMVar_ID_41579 Human_SNP_ID_554686842 A-to-I Human chr14 - 49819104 49819104 49819104 GCACCCTCCTTTTCTTTTTTTCTTTTGGAGACAGAGTTTCGCTCTGTGGCACAGGCTGCTGAGTA GCACCCTCCTTTTCTTTTTTTCTTTTGGAGACGGAGTTTCGCTCTGTGGCACAGGCTGCTGAGTA T C NEMF Ensembl:ENSG00000165525 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1018663039 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76409,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_1277,RMVar_hsa_circ_359769,RMVar_hsa_circ_308326,RMVar_hsa_circ_74853,RMVar_hsa_circ_310361,RMVar_hsa_circ_166357,RMVar_hsa_circ_368230,RMVar_hsa_circ_323169,RMVar_hsa_circ_333912,RMVar_hsa_circ_296132,RMVar_hsa_circ_73505,RMVar_hsa_circ_10183,RMVar_hsa_circ_166362,RMVar_hsa_circ_166363,RMVar_hsa_circ_166364,RMVar_hsa_circ_379010,RMVar_hsa_circ_349111,RMVar_hsa_circ_303566,RMVar_hsa_circ_306001,RMVar_hsa_circ_166366,RMVar_hsa_circ_166367,RMVar_hsa_circ_28810,RMVar_hsa_circ_316624,RMVar_hsa_circ_345075,RMVar_hsa_circ_166372,RMVar_hsa_circ_166373,RMVar_hsa_circ_43596,RMVar_hsa_circ_372451,RMVar_hsa_circ_323871,RMVar_hsa_circ_360485,RMVar_hsa_circ_330309,RMVar_hsa_circ_166374,RMVar_hsa_circ_23477,RMVar_hsa_circ_23820,RMVar_hsa_circ_166376,RMVar_hsa_circ_166375,RMVar_hsa_circ_25136,RMVar_hsa_circ_283554,RMVar_hsa_circ_305324,RMVar_hsa_circ_38588,RMVar_hsa_circ_15462,RMVar_hsa_circ_166378,RMVar_hsa_circ_166379,RMVar_hsa_circ_166381,RMVar_hsa_circ_266893,RMVar_hsa_circ_332814,RMVar_hsa_circ_46834,RMVar_hsa_circ_166380 41580 RMVar_ID_41580 Human_SNP_ID_554687004 A-to-I Human chr14 - 49819617 49819617 49819617 CTGAGGTGAGGAGTTCGAGACCAGCCTGGGCAACATGGCGAAACCCCGTCTCTACAAAAATACAA CTGAGGTGAGGAGTTCGAGACCAGCCTGGGCAGCATGGCGAAACCCCGTCTCTACAAAAATACAA T C NEMF Ensembl:ENSG00000165525 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs904666770 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76409,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_1277,RMVar_hsa_circ_359769,RMVar_hsa_circ_308326,RMVar_hsa_circ_74853,RMVar_hsa_circ_310361,RMVar_hsa_circ_166357,RMVar_hsa_circ_368230,RMVar_hsa_circ_323169,RMVar_hsa_circ_333912,RMVar_hsa_circ_296132,RMVar_hsa_circ_73505,RMVar_hsa_circ_10183,RMVar_hsa_circ_166362,RMVar_hsa_circ_166363,RMVar_hsa_circ_166364,RMVar_hsa_circ_379010,RMVar_hsa_circ_349111,RMVar_hsa_circ_303566,RMVar_hsa_circ_306001,RMVar_hsa_circ_166366,RMVar_hsa_circ_166367,RMVar_hsa_circ_28810,RMVar_hsa_circ_316624,RMVar_hsa_circ_345075,RMVar_hsa_circ_166372,RMVar_hsa_circ_166373,RMVar_hsa_circ_43596,RMVar_hsa_circ_372451,RMVar_hsa_circ_323871,RMVar_hsa_circ_360485,RMVar_hsa_circ_330309,RMVar_hsa_circ_166374,RMVar_hsa_circ_23477,RMVar_hsa_circ_23820,RMVar_hsa_circ_166376,RMVar_hsa_circ_166375,RMVar_hsa_circ_25136,RMVar_hsa_circ_283554,RMVar_hsa_circ_305324,RMVar_hsa_circ_38588,RMVar_hsa_circ_15462,RMVar_hsa_circ_166378,RMVar_hsa_circ_166379,RMVar_hsa_circ_166381,RMVar_hsa_circ_266893,RMVar_hsa_circ_332814,RMVar_hsa_circ_46834,RMVar_hsa_circ_166380 41581 RMVar_ID_41581 Human_SNP_ID_554687148 A-to-I Human chr14 - 49820084 49820084 49820084 AGCCAGGTGTGGTGGCTTGTGCCTGTAGACCAAGCTACTCGGGTGGCTGAGGCAGAAGAATCGCT AGCCAGGTGTGGTGGCTTGTGCCTGTAGACCAGGCTACTCGGGTGGCTGAGGCAGAAGAATCGCT T C NEMF Ensembl:ENSG00000165525 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1360253241 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76409,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_1277,RMVar_hsa_circ_359769,RMVar_hsa_circ_308326,RMVar_hsa_circ_74853,RMVar_hsa_circ_310361,RMVar_hsa_circ_166357,RMVar_hsa_circ_368230,RMVar_hsa_circ_323169,RMVar_hsa_circ_333912,RMVar_hsa_circ_296132,RMVar_hsa_circ_73505,RMVar_hsa_circ_10183,RMVar_hsa_circ_166362,RMVar_hsa_circ_166363,RMVar_hsa_circ_166364,RMVar_hsa_circ_379010,RMVar_hsa_circ_349111,RMVar_hsa_circ_303566,RMVar_hsa_circ_306001,RMVar_hsa_circ_166366,RMVar_hsa_circ_166367,RMVar_hsa_circ_28810,RMVar_hsa_circ_316624,RMVar_hsa_circ_345075,RMVar_hsa_circ_166372,RMVar_hsa_circ_166373,RMVar_hsa_circ_43596,RMVar_hsa_circ_372451,RMVar_hsa_circ_323871,RMVar_hsa_circ_360485,RMVar_hsa_circ_330309,RMVar_hsa_circ_166374,RMVar_hsa_circ_23477,RMVar_hsa_circ_23820,RMVar_hsa_circ_166376,RMVar_hsa_circ_166375,RMVar_hsa_circ_25136,RMVar_hsa_circ_283554,RMVar_hsa_circ_305324,RMVar_hsa_circ_38588,RMVar_hsa_circ_15462,RMVar_hsa_circ_166378,RMVar_hsa_circ_166379,RMVar_hsa_circ_166381,RMVar_hsa_circ_266893,RMVar_hsa_circ_332814,RMVar_hsa_circ_46834,RMVar_hsa_circ_166380 41582 RMVar_ID_41582 Human_SNP_ID_554687154 A-to-I Human chr14 - 49820112 49820112 49820112 CCCCGTTTCTACTAAAAATACAAAAATTAGCCAGGTGTGGTGGCTTGTGCCTGTAGACCAAGCTA CCCCGTTTCTACTAAAAATACAAAAATTAGCCGGGTGTGGTGGCTTGTGCCTGTAGACCAAGCTA T C NEMF Ensembl:ENSG00000165525 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1190617377 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76409,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_1277,RMVar_hsa_circ_359769,RMVar_hsa_circ_308326,RMVar_hsa_circ_74853,RMVar_hsa_circ_310361,RMVar_hsa_circ_166357,RMVar_hsa_circ_368230,RMVar_hsa_circ_323169,RMVar_hsa_circ_333912,RMVar_hsa_circ_296132,RMVar_hsa_circ_73505,RMVar_hsa_circ_10183,RMVar_hsa_circ_166362,RMVar_hsa_circ_166363,RMVar_hsa_circ_166364,RMVar_hsa_circ_379010,RMVar_hsa_circ_349111,RMVar_hsa_circ_303566,RMVar_hsa_circ_306001,RMVar_hsa_circ_166366,RMVar_hsa_circ_166367,RMVar_hsa_circ_28810,RMVar_hsa_circ_316624,RMVar_hsa_circ_345075,RMVar_hsa_circ_166372,RMVar_hsa_circ_166373,RMVar_hsa_circ_43596,RMVar_hsa_circ_372451,RMVar_hsa_circ_323871,RMVar_hsa_circ_360485,RMVar_hsa_circ_330309,RMVar_hsa_circ_166374,RMVar_hsa_circ_23477,RMVar_hsa_circ_23820,RMVar_hsa_circ_166376,RMVar_hsa_circ_166375,RMVar_hsa_circ_25136,RMVar_hsa_circ_283554,RMVar_hsa_circ_305324,RMVar_hsa_circ_38588,RMVar_hsa_circ_15462,RMVar_hsa_circ_113217,RMVar_hsa_circ_166378,RMVar_hsa_circ_166379,RMVar_hsa_circ_166381,RMVar_hsa_circ_266893,RMVar_hsa_circ_332814,RMVar_hsa_circ_46834,RMVar_hsa_circ_166380,RMVar_hsa_circ_166382 41583 RMVar_ID_41583 Human_SNP_ID_554690883 A-to-I Human chr14 - 49833049 49833049 49833049 GTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAAGTGATCCGCCTGCCTTGGCCTCCCAAAGTGC GTTGGCCAGGCTGGTCTCGAACTCCTGACCTCGAGTGATCCGCCTGCCTTGGCCTCCCAAAGTGC T C NEMF Ensembl:ENSG00000165525 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1368889184 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76409,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_1277,RMVar_hsa_circ_359769,RMVar_hsa_circ_74853,RMVar_hsa_circ_310361,RMVar_hsa_circ_368230,RMVar_hsa_circ_333912,RMVar_hsa_circ_166385,RMVar_hsa_circ_10183,RMVar_hsa_circ_166364,RMVar_hsa_circ_379010,RMVar_hsa_circ_303566,RMVar_hsa_circ_316624,RMVar_hsa_circ_166372,RMVar_hsa_circ_43596,RMVar_hsa_circ_360485,RMVar_hsa_circ_166374,RMVar_hsa_circ_23820,RMVar_hsa_circ_283554,RMVar_hsa_circ_15462,RMVar_hsa_circ_295878,RMVar_hsa_circ_166379,RMVar_hsa_circ_166381,RMVar_hsa_circ_46834,RMVar_hsa_circ_166383,RMVar_hsa_circ_311377,RMVar_hsa_circ_315375,RMVar_hsa_circ_288456,RMVar_hsa_circ_166386,RMVar_hsa_circ_166394,RMVar_hsa_circ_13552,RMVar_hsa_circ_12921,RMVar_hsa_circ_166384,RMVar_hsa_circ_295418,RMVar_hsa_circ_338699,RMVar_hsa_circ_166390,RMVar_hsa_circ_334197,RMVar_hsa_circ_166392,RMVar_hsa_circ_276601,RMVar_hsa_circ_323231,RMVar_hsa_circ_327770,RMVar_hsa_circ_31956,RMVar_hsa_circ_166393 41584 RMVar_ID_41584 Human_SNP_ID_554690893 A-to-I Human chr14 - 49833061 49833061 49833061 AGGTTTCACCGTGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAAGTGATCCGCCTGCCTTGGC AGGTTTCACCGTGTTGGCCAGGCTGGTCTCGAGCTCCTGACCTCAAGTGATCCGCCTGCCTTGGC T C NEMF Ensembl:ENSG00000165525 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1415154655 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76409,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_1277,RMVar_hsa_circ_359769,RMVar_hsa_circ_74853,RMVar_hsa_circ_310361,RMVar_hsa_circ_368230,RMVar_hsa_circ_333912,RMVar_hsa_circ_166385,RMVar_hsa_circ_10183,RMVar_hsa_circ_166364,RMVar_hsa_circ_379010,RMVar_hsa_circ_303566,RMVar_hsa_circ_316624,RMVar_hsa_circ_166372,RMVar_hsa_circ_43596,RMVar_hsa_circ_360485,RMVar_hsa_circ_166374,RMVar_hsa_circ_23820,RMVar_hsa_circ_283554,RMVar_hsa_circ_15462,RMVar_hsa_circ_295878,RMVar_hsa_circ_166379,RMVar_hsa_circ_166381,RMVar_hsa_circ_46834,RMVar_hsa_circ_166383,RMVar_hsa_circ_311377,RMVar_hsa_circ_315375,RMVar_hsa_circ_288456,RMVar_hsa_circ_166386,RMVar_hsa_circ_166394,RMVar_hsa_circ_13552,RMVar_hsa_circ_12921,RMVar_hsa_circ_166384,RMVar_hsa_circ_295418,RMVar_hsa_circ_338699,RMVar_hsa_circ_166390,RMVar_hsa_circ_334197,RMVar_hsa_circ_166392,RMVar_hsa_circ_276601,RMVar_hsa_circ_323231,RMVar_hsa_circ_327770,RMVar_hsa_circ_31956,RMVar_hsa_circ_166393 41585 RMVar_ID_41585 Human_SNP_ID_554690924 A-to-I Human chr14 - 49833184 49833184 49833184 TTGGCTCATTGCAACCTCTGCTTCCCTGGTTGAAGTGATTCTCCTGTCTCAGCCTCCCGAGTAGC TTGGCTCATTGCAACCTCTGCTTCCCTGGTTGGAGTGATTCTCCTGTCTCAGCCTCCCGAGTAGC T C NEMF Ensembl:ENSG00000165525 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1416925605 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76409,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_1277,RMVar_hsa_circ_359769,RMVar_hsa_circ_74853,RMVar_hsa_circ_310361,RMVar_hsa_circ_368230,RMVar_hsa_circ_333912,RMVar_hsa_circ_166385,RMVar_hsa_circ_10183,RMVar_hsa_circ_166364,RMVar_hsa_circ_379010,RMVar_hsa_circ_303566,RMVar_hsa_circ_316624,RMVar_hsa_circ_166372,RMVar_hsa_circ_43596,RMVar_hsa_circ_360485,RMVar_hsa_circ_166374,RMVar_hsa_circ_23820,RMVar_hsa_circ_283554,RMVar_hsa_circ_15462,RMVar_hsa_circ_295878,RMVar_hsa_circ_166379,RMVar_hsa_circ_166381,RMVar_hsa_circ_46834,RMVar_hsa_circ_166383,RMVar_hsa_circ_311377,RMVar_hsa_circ_315375,RMVar_hsa_circ_288456,RMVar_hsa_circ_166386,RMVar_hsa_circ_166394,RMVar_hsa_circ_13552,RMVar_hsa_circ_12921,RMVar_hsa_circ_166384,RMVar_hsa_circ_295418,RMVar_hsa_circ_338699,RMVar_hsa_circ_166390,RMVar_hsa_circ_334197,RMVar_hsa_circ_166392,RMVar_hsa_circ_276601,RMVar_hsa_circ_323231,RMVar_hsa_circ_327770,RMVar_hsa_circ_31956,RMVar_hsa_circ_166393 41586 RMVar_ID_41586 Human_SNP_ID_554691363 A-to-I Human chr14 - 49834611 49834611 49834611 GGGCATGGTGGTGGGTGCTTGTGATCCCAGCTACTCAGGAGGCTGAGGCAGGAGGTGGGAGGCAG GGGCATGGTGGTGGGTGCTTGTGATCCCAGCTGCTCAGGAGGCTGAGGCAGGAGGTGGGAGGCAG T C NEMF Ensembl:ENSG00000165525 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170483043 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76409,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_1277,RMVar_hsa_circ_368230,RMVar_hsa_circ_10183,RMVar_hsa_circ_379010,RMVar_hsa_circ_23820,RMVar_hsa_circ_15462,RMVar_hsa_circ_311377,RMVar_hsa_circ_315375,RMVar_hsa_circ_166394,RMVar_hsa_circ_166384,RMVar_hsa_circ_338699,RMVar_hsa_circ_323231,RMVar_hsa_circ_327770,RMVar_hsa_circ_166397,RMVar_hsa_circ_309772,RMVar_hsa_circ_278048,RMVar_hsa_circ_313092,RMVar_hsa_circ_356261,RMVar_hsa_circ_166398,RMVar_hsa_circ_166396 41587 RMVar_ID_41587 Human_SNP_ID_554691404 A-to-I Human chr14 - 49834739 49834739 49834739 GTGGCCCACACCTGTAATCTGAGCACTTTTGGAGGTTGAGGTGAGTGGATCACCTGAGGTTAGGA GTGGCCCACACCTGTAATCTGAGCACTTTTGGCGGTTGAGGTGAGTGGATCACCTGAGGTTAGGA T G NEMF Ensembl:ENSG00000165525 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs974349696 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76409,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_1277,RMVar_hsa_circ_368230,RMVar_hsa_circ_10183,RMVar_hsa_circ_379010,RMVar_hsa_circ_23820,RMVar_hsa_circ_15462,RMVar_hsa_circ_311377,RMVar_hsa_circ_315375,RMVar_hsa_circ_166394,RMVar_hsa_circ_166384,RMVar_hsa_circ_338699,RMVar_hsa_circ_323231,RMVar_hsa_circ_327770,RMVar_hsa_circ_166397,RMVar_hsa_circ_309772,RMVar_hsa_circ_278048,RMVar_hsa_circ_313092,RMVar_hsa_circ_356261,RMVar_hsa_circ_166398,RMVar_hsa_circ_166396 41588 RMVar_ID_41588 Human_SNP_ID_554691410 A-to-I Human chr14 - 49834779 49834779 49834779 TGTGCTATATTTTGAATGTTAAATTTTAGGCTAGGTCATGGTGGCCCACACCTGTAATCTGAGCA TGTGCTATATTTTGAATGTTAAATTTTAGGCTTGGTCATGGTGGCCCACACCTGTAATCTGAGCA T A NEMF Ensembl:ENSG00000165525 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs930137172 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76409,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_1277,RMVar_hsa_circ_368230,RMVar_hsa_circ_10183,RMVar_hsa_circ_379010,RMVar_hsa_circ_23820,RMVar_hsa_circ_15462,RMVar_hsa_circ_311377,RMVar_hsa_circ_315375,RMVar_hsa_circ_166394,RMVar_hsa_circ_166384,RMVar_hsa_circ_338699,RMVar_hsa_circ_323231,RMVar_hsa_circ_327770,RMVar_hsa_circ_166397,RMVar_hsa_circ_309772,RMVar_hsa_circ_278048,RMVar_hsa_circ_313092,RMVar_hsa_circ_356261,RMVar_hsa_circ_166398,RMVar_hsa_circ_166396 41589 RMVar_ID_41589 Human_SNP_ID_554691411 A-to-I Human chr14 - 49834779 49834779 49834779 TGTGCTATATTTTGAATGTTAAATTTTAGGCTAGGTCATGGTGGCCCACACCTGTAATCTGAGCA TGTGCTATATTTTGAATGTTAAATTTTAGGCTGGGTCATGGTGGCCCACACCTGTAATCTGAGCA T C NEMF Ensembl:ENSG00000165525 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs930137172 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76409,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_1277,RMVar_hsa_circ_368230,RMVar_hsa_circ_10183,RMVar_hsa_circ_379010,RMVar_hsa_circ_23820,RMVar_hsa_circ_15462,RMVar_hsa_circ_311377,RMVar_hsa_circ_315375,RMVar_hsa_circ_166394,RMVar_hsa_circ_166384,RMVar_hsa_circ_338699,RMVar_hsa_circ_323231,RMVar_hsa_circ_327770,RMVar_hsa_circ_166397,RMVar_hsa_circ_309772,RMVar_hsa_circ_278048,RMVar_hsa_circ_313092,RMVar_hsa_circ_356261,RMVar_hsa_circ_166398,RMVar_hsa_circ_166396 41590 RMVar_ID_41590 Human_SNP_ID_554693827 A-to-I Human chr14 - 49842835 49842833 49842835 CGCCCAGCTAGTTTTTGTACTCTTAGTAAAACAGGGATTCACCATGTTGGCCAGTCTGGTCTTGA CGCCCAGCTAGTTTTTGTACTCTTAGTAAAAC__GGATTCACCATGTTGGCCAGTCTGGTCTTGA CCT C NEMF Ensembl:ENSG00000165525 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1441661453 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_76409,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_1277,RMVar_hsa_circ_356261,RMVar_hsa_circ_166398,RMVar_hsa_circ_13910,RMVar_hsa_circ_303342,RMVar_hsa_circ_166399,RMVar_hsa_circ_315934,RMVar_hsa_circ_166400 41591 RMVar_ID_41591 Human_SNP_ID_554697170 A-to-I Human chr14 + 49853630 49853630 49853630 ATAAGGTGAGAACTCAAAAGAGGCAGGGTCTCACTATGTTGCCCAGGCTGGAGTGCAGTGGCTAT ATAAGGTGAGAACTCAAAAGAGGCAGGGTCTCGCTATGTTGCCCAGGCTGGAGTGCAGTGGCTAT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1230709169 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 41592 RMVar_ID_41592 Human_SNP_ID_554698334 A-to-I Human chr14 - 49858313 49858312 49858313 TTACTTTCTTTTTTTTTTTTTTTTTTTTTTTGAGACGGGGTCTTTCTCTGTCACCCAGGCTAGAG TTACTTTCTTTTTTTTTTTTTTTTTTTTTTTG_GACGGGGTCTTTCTCTGTCACCCAGGCTAGAG CT C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334944950 Functional Loss DEL dbSNP153 33..33 33 - - - 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 41593 RMVar_ID_41593 Human_SNP_ID_554747441 A-to-I Human chr14 - 50050684 50050684 50050684 TTCCTATGTGCAGGACCTCCTGGGGTTCAGAGACTAAATTCATCTTGTATGGACGACACTTCTCT TTCCTATGTGCAGGACCTCCTGGGGTTCAGAGGCTAAATTCATCTTGTATGGACGACACTTCTCT T C LINC01588 Ensembl:ENSG00000214900 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1225914034 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_166404,RMVar_hsa_circ_64407,RMVar_hsa_circ_329079,RMVar_hsa_circ_307436,RMVar_hsa_circ_312986,RMVar_hsa_circ_166405 41594 RMVar_ID_41594 Human_SNP_ID_554747535 A-to-I Human chr14 + 50051007 50051007 50051007 CAAAACAGTCTGTGTCTTTTCTGGTTTTGCAGAAAATCCTGGAGTCTGAAGAAAAAGAGGATCCC CAAAACAGTCTGTGTCTTTTCTGGTTTTGCAGGAAATCCTGGAGTCTGAAGAAAAAGAGGATCCC A G PDLIM1P1 Ensembl:ENSG00000270788 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1390369048 Functional Loss SNV dbSNP153 33..33 33 - - - 41595 RMVar_ID_41595 Human_SNP_ID_554747542 A-to-I Human chr14 + 50051032 50051032 50051032 TTTGCAGAAAATCCTGGAGTCTGAAGAAAAAGAGGATCCCAACAAGCCCTCAGGATTCAGAAGTG TTTGCAGAAAATCCTGGAGTCTGAAGAAAAAGGGGATCCCAACAAGCCCTCAGGATTCAGAAGTG A G PDLIM1P1 Ensembl:ENSG00000270788 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968268113 Functional Loss SNV dbSNP153 33..33 33 - - - 41596 RMVar_ID_41596 Human_SNP_ID_554762895 A-to-I Human chr14 - 50110011 50110010 50110012 CGAACTCCTGGCCTCAAGTGCTCTGCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG CGAACTCCTGGCCTCAAGTGCTCTGCCACCT__GCCTCCCAAAGTGCTGGGATTACAGGTGTGAG CTG C VCPKMT Ensembl:ENSG00000100483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1302182078 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_12341476 41597 RMVar_ID_41597 Human_SNP_ID_554764496 A-to-I Human chr14 - 50114726 50114726 50114726 TCCCATTCAGCCTCCTCAATAGCTGGGACTATAGGTGTGCACCAGCATGCTGGCTAATTTTTAAA TCCCATTCAGCCTCCTCAATAGCTGGGACTATGGGTGTGCACCAGCATGCTGGCTAATTTTTAAA T C VCPKMT Ensembl:ENSG00000100483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256370483 Functional Loss SNV dbSNP153 33..33 33 - - - 41598 RMVar_ID_41598 Human_SNP_ID_554764498 A-to-I Human chr14 - 50114728 50114728 50114728 CCTCCCATTCAGCCTCCTCAATAGCTGGGACTATAGGTGTGCACCAGCATGCTGGCTAATTTTTA CCTCCCATTCAGCCTCCTCAATAGCTGGGACTGTAGGTGTGCACCAGCATGCTGGCTAATTTTTA T C VCPKMT Ensembl:ENSG00000100483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1233219109 Functional Loss SNV dbSNP153 33..33 33 - - - 41599 RMVar_ID_41599 Human_SNP_ID_554776853 A-to-I Human chr14 - 50161185 50161185 50161185 GCGTTCCAATGATTCTCCTGCCTTCGCCTCCCAAGTAACTGGAACTACAGGAGCCCACCACCATG GCGTTCCAATGATTCTCCTGCCTTCGCCTCCCGAGTAACTGGAACTACAGGAGCCCACCACCATG T C SOS2 Ensembl:ENSG00000100485 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1242203126 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_882,RMVar_hsa_circ_4561,RMVar_hsa_circ_364959,RMVar_hsa_circ_92072,RMVar_hsa_circ_93929,RMVar_hsa_circ_27177,RMVar_hsa_circ_3497,RMVar_hsa_circ_166409,RMVar_hsa_circ_166408,RMVar_hsa_circ_19219,RMVar_hsa_circ_22481,RMVar_hsa_circ_26113,RMVar_hsa_circ_304397,RMVar_hsa_circ_31194,RMVar_hsa_circ_28874,RMVar_hsa_circ_26744,RMVar_hsa_circ_289323,RMVar_hsa_circ_317333,RMVar_hsa_circ_330518,RMVar_hsa_circ_13057,RMVar_hsa_circ_20037,RMVar_hsa_circ_166438,RMVar_hsa_circ_10486,RMVar_hsa_circ_295742,RMVar_hsa_circ_315037,RMVar_hsa_circ_345497,RMVar_hsa_circ_21734,RMVar_hsa_circ_166441,RMVar_hsa_circ_166443,RMVar_hsa_circ_293708,RMVar_hsa_circ_341497,RMVar_hsa_circ_264783 41600 RMVar_ID_41600 Human_SNP_ID_554776880 A-to-I Human chr14 - 50161253 50161253 50161253 CTCTCTTGCCCAGGCTGGAGTGCAGTGGTGTAATCTCAGCTCACTGCAACCTGCAGCCTTAGCCT CTCTCTTGCCCAGGCTGGAGTGCAGTGGTGTAGTCTCAGCTCACTGCAACCTGCAGCCTTAGCCT T C SOS2 Ensembl:ENSG00000100485 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1276064863 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_882,RMVar_hsa_circ_4561,RMVar_hsa_circ_364959,RMVar_hsa_circ_92072,RMVar_hsa_circ_93929,RMVar_hsa_circ_27177,RMVar_hsa_circ_3497,RMVar_hsa_circ_166409,RMVar_hsa_circ_166408,RMVar_hsa_circ_19219,RMVar_hsa_circ_22481,RMVar_hsa_circ_26113,RMVar_hsa_circ_304397,RMVar_hsa_circ_31194,RMVar_hsa_circ_28874,RMVar_hsa_circ_26744,RMVar_hsa_circ_289323,RMVar_hsa_circ_317333,RMVar_hsa_circ_330518,RMVar_hsa_circ_13057,RMVar_hsa_circ_20037,RMVar_hsa_circ_166438,RMVar_hsa_circ_10486,RMVar_hsa_circ_295742,RMVar_hsa_circ_315037,RMVar_hsa_circ_345497,RMVar_hsa_circ_21734,RMVar_hsa_circ_166441,RMVar_hsa_circ_166443,RMVar_hsa_circ_293708,RMVar_hsa_circ_341497,RMVar_hsa_circ_264783 41601 RMVar_ID_41601 Human_SNP_ID_554786715 A-to-I Human chr14 - 50197008 50197008 50197008 AAAAAAAATTATCCGGGCGTGTGCTTGTGACTATAGTCCCAGCTATTTGGGAGGCTGAGGTGGGA AAAAAAAATTATCCGGGCGTGTGCTTGTGACTGTAGTCCCAGCTATTTGGGAGGCTGAGGTGGGA T C SOS2 Ensembl:ENSG00000100485 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017406459 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23624161 RMVar_hsa_circ_92072,RMVar_hsa_circ_27177,RMVar_hsa_circ_3497,RMVar_hsa_circ_166408,RMVar_hsa_circ_19219,RMVar_hsa_circ_26113,RMVar_hsa_circ_28874,RMVar_hsa_circ_26744,RMVar_hsa_circ_166450,RMVar_hsa_circ_4648,RMVar_hsa_circ_295742,RMVar_hsa_circ_21734,RMVar_hsa_circ_166441,RMVar_hsa_circ_13438,RMVar_hsa_circ_166446,RMVar_hsa_circ_297773,RMVar_hsa_circ_342969,RMVar_hsa_circ_294239,RMVar_hsa_circ_166447,RMVar_hsa_circ_343918,RMVar_hsa_circ_306969,RMVar_hsa_circ_273101,RMVar_hsa_circ_166448,RMVar_hsa_circ_166449,RMVar_hsa_circ_166457,RMVar_hsa_circ_371389,RMVar_hsa_circ_298243,RMVar_hsa_circ_166456,RMVar_hsa_circ_303612,RMVar_hsa_circ_309224,RMVar_hsa_circ_166458,RMVar_hsa_circ_166459,RMVar_hsa_circ_166462 41602 RMVar_ID_41602 Human_SNP_ID_554787259 A-to-I Human chr14 - 50199031 50199031 50199031 CTCCTATCTCAGCCTCTCGAGTAGCTAGGACCACAGGCGTGCATCACCACGTCCAGCTGTTTTTA CTCCTATCTCAGCCTCTCGAGTAGCTAGGACCGCAGGCGTGCATCACCACGTCCAGCTGTTTTTA T C SOS2 Ensembl:ENSG00000100485 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs761397406 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92072,RMVar_hsa_circ_27177,RMVar_hsa_circ_3497,RMVar_hsa_circ_166408,RMVar_hsa_circ_19219,RMVar_hsa_circ_26113,RMVar_hsa_circ_28874,RMVar_hsa_circ_26744,RMVar_hsa_circ_166450,RMVar_hsa_circ_4648,RMVar_hsa_circ_295742,RMVar_hsa_circ_21734,RMVar_hsa_circ_166441,RMVar_hsa_circ_13438,RMVar_hsa_circ_166446,RMVar_hsa_circ_297773,RMVar_hsa_circ_342969,RMVar_hsa_circ_294239,RMVar_hsa_circ_166447,RMVar_hsa_circ_343918,RMVar_hsa_circ_306969,RMVar_hsa_circ_273101,RMVar_hsa_circ_166448,RMVar_hsa_circ_166449,RMVar_hsa_circ_166457,RMVar_hsa_circ_371389,RMVar_hsa_circ_298243,RMVar_hsa_circ_166456,RMVar_hsa_circ_303612,RMVar_hsa_circ_309224,RMVar_hsa_circ_166458,RMVar_hsa_circ_166459,RMVar_hsa_circ_166462 41603 RMVar_ID_41603 Human_SNP_ID_554787262 A-to-I Human chr14 - 50199037 50199037 50199037 GCGATCCTCCTATCTCAGCCTCTCGAGTAGCTAGGACCACAGGCGTGCATCACCACGTCCAGCTG GCGATCCTCCTATCTCAGCCTCTCGAGTAGCTGGGACCACAGGCGTGCATCACCACGTCCAGCTG T C SOS2 Ensembl:ENSG00000100485 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs906528226 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92072,RMVar_hsa_circ_27177,RMVar_hsa_circ_3497,RMVar_hsa_circ_166408,RMVar_hsa_circ_19219,RMVar_hsa_circ_26113,RMVar_hsa_circ_28874,RMVar_hsa_circ_26744,RMVar_hsa_circ_166450,RMVar_hsa_circ_4648,RMVar_hsa_circ_295742,RMVar_hsa_circ_21734,RMVar_hsa_circ_166441,RMVar_hsa_circ_13438,RMVar_hsa_circ_166446,RMVar_hsa_circ_297773,RMVar_hsa_circ_342969,RMVar_hsa_circ_294239,RMVar_hsa_circ_166447,RMVar_hsa_circ_343918,RMVar_hsa_circ_306969,RMVar_hsa_circ_273101,RMVar_hsa_circ_166448,RMVar_hsa_circ_166449,RMVar_hsa_circ_166457,RMVar_hsa_circ_371389,RMVar_hsa_circ_298243,RMVar_hsa_circ_166456,RMVar_hsa_circ_303612,RMVar_hsa_circ_309224,RMVar_hsa_circ_166458,RMVar_hsa_circ_166459,RMVar_hsa_circ_166462 41604 RMVar_ID_41604 Human_SNP_ID_554788066 A-to-I Human chr14 - 50202091 50202091 50202091 AAGAGTAGGGGTATGTGCTTGTAGTCCCAGCTACTCGGGATGCTGAGGTGGGAGGATCATTGGAG AAGAGTAGGGGTATGTGCTTGTAGTCCCAGCTGCTCGGGATGCTGAGGTGGGAGGATCATTGGAG T C SOS2 Ensembl:ENSG00000100485 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1183439248 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3497,RMVar_hsa_circ_19219,RMVar_hsa_circ_26113,RMVar_hsa_circ_28874,RMVar_hsa_circ_26744,RMVar_hsa_circ_295742,RMVar_hsa_circ_166441,RMVar_hsa_circ_13438,RMVar_hsa_circ_297773,RMVar_hsa_circ_166447,RMVar_hsa_circ_273101,RMVar_hsa_circ_166448,RMVar_hsa_circ_166457,RMVar_hsa_circ_298243,RMVar_hsa_circ_309224,RMVar_hsa_circ_166458,RMVar_hsa_circ_166462,RMVar_hsa_circ_293997,RMVar_hsa_circ_166464,RMVar_hsa_circ_166463,RMVar_hsa_circ_271285 41605 RMVar_ID_41605 Human_SNP_ID_554795350 A-to-I Human chr14 - 50228322 50228322 50228322 TTACTTGCATCTCAGTGGGCGTGGTGGCTCACACCTGTAATCCAGCACTCTGGGAGGCTGAGGCT TTACTTGCATCTCAGTGGGCGTGGTGGCTCACGCCTGTAATCCAGCACTCTGGGAGGCTGAGGCT T C SOS2 Ensembl:ENSG00000100485 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1371471491 Functional Loss SNV dbSNP153 33..33 33 - - - 41606 RMVar_ID_41606 Human_SNP_ID_554798268 A-to-I Human chr14 - 50238548 50238548 50238548 AGCTCAACCAGAATCTACTTCATTAGCTTTCCAATGATTCTGTATTCTCTGAACGAATGTATTAT AGCTCAACCAGAATCTACTTCATTAGCTTTCCCATGATTCTGTATTCTCTGAACGAATGTATTAT T G L2HGDH Ensembl:ENSG00000087299 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1308926570 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_166465 41607 RMVar_ID_41607 Human_SNP_ID_554798270 A-to-I Human chr14 - 50238556 50238556 50238556 TTCCTGAAAGCTCAACCAGAATCTACTTCATTAGCTTTCCAATGATTCTGTATTCTCTGAACGAA TTCCTGAAAGCTCAACCAGAATCTACTTCATTGGCTTTCCAATGATTCTGTATTCTCTGAACGAA T C L2HGDH Ensembl:ENSG00000087299 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs865932355 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_166465 41608 RMVar_ID_41608 Human_SNP_ID_554800161 A-to-I Human chr14 - 50246084 50246084 50246084 AGTTTCACTCTTGTTGCCCAGGCTTGAGTGCAATGGTACGATCTTGGCTCACTGCAACCTCTGCC AGTTTCACTCTTGTTGCCCAGGCTTGAGTGCAGTGGTACGATCTTGGCTCACTGCAACCTCTGCC T C L2HGDH Ensembl:ENSG00000087299 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1566497440 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1512442 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 41609 RMVar_ID_41609 Human_SNP_ID_554800226 A-to-I Human chr14 - 50246273 50246273 50246273 TCAAGGCTACAGTGAGCTGTGTTCATGCCACTATACCCCAGCCTGGGCAACAAAGTGAGTCCCTG TCAAGGCTACAGTGAGCTGTGTTCATGCCACTGTACCCCAGCCTGGGCAACAAAGTGAGTCCCTG T C L2HGDH Ensembl:ENSG00000087299 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,31158229,32596459 RNA-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 41610 RMVar_ID_41610 Human_SNP_ID_554800257 A-to-I Human chr14 - 50246371 50246371 50246371 TCTACAAAAAATACAAAAATTAGCTGGGCATGATGGTGTGTGCCTGTAGTCCCAGCTACTTGGGG TCTACAAAAAATACAAAAATTAGCTGGGCATGGTGGTGTGTGCCTGTAGTCCCAGCTACTTGGGG T C L2HGDH Ensembl:ENSG00000087299 Protein coding intron GSE38233;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,32596459 RNA-Seq:(High) rs1367274923 Functional Loss SNV dbSNP153 33..33 33 - - - 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 41611 RMVar_ID_41611 Human_SNP_ID_554800260 A-to-I Human chr14 - 50246388 50246388 50246388 GTGAATGAAACCCCATCTCTACAAAAAATACAAAAATTAGCTGGGCATGATGGTGTGTGCCTGTA GTGAATGAAACCCCATCTCTACAAAAAATACAGAAATTAGCTGGGCATGATGGTGTGTGCCTGTA T C L2HGDH Ensembl:ENSG00000087299 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1047707179 Functional Loss SNV dbSNP153 33..33 33 - - - 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 41612 RMVar_ID_41612 Human_SNP_ID_554800322 A-to-I Human chr14 - 50246572 50246572 50246572 TGGGTCTGGTGCCTCTGTAGTTCCAGCTCCTCAGTAGGCTGAGGTGAGAGGATCACTTGAGCCCA TGGGTCTGGTGCCTCTGTAGTTCCAGCTCCTCGGTAGGCTGAGGTGAGAGGATCACTTGAGCCCA T C L2HGDH Ensembl:ENSG00000087299 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs950172455 Functional Loss SNV dbSNP153 33..33 33 - - - 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 41613 RMVar_ID_41613 Human_SNP_ID_554803956 A-to-I Human chr14 - 50261555 50261555 50261555 TCCCTTGAGCCCAGGATGCTGAAGCTACAGTTAGCCATTATTGCACTACTGTCCTCCAGCCTGGT TCCCTTGAGCCCAGGATGCTGAAGCTACAGTTGGCCATTATTGCACTACTGTCCTCCAGCCTGGT T C L2HGDH Ensembl:ENSG00000087299 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs912326098 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_166465,RMVar_hsa_circ_268325,RMVar_hsa_circ_24859,RMVar_hsa_circ_83950,RMVar_hsa_circ_166468,RMVar_hsa_circ_293326,RMVar_hsa_circ_305972,RMVar_hsa_circ_354939,RMVar_hsa_circ_296242,RMVar_hsa_circ_166469,RMVar_hsa_circ_11712,RMVar_hsa_circ_21719,RMVar_hsa_circ_166470,RMVar_hsa_circ_166471 41614 RMVar_ID_41614 Human_SNP_ID_554811020 A-to-I Human chr14 - 50289470 50289470 50289470 AAAGCTAATTAGATCTTTAAACTAAATTTGTTATAATTTTGTCTTTTAACACACTCAATGGTTTT AAAGCTAATTAGATCTTTAAACTAAATTTGTTGTAATTTTGTCTTTTAACACACTCAATGGTTTT T C L2HGDH Ensembl:ENSG00000087299 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1441197545 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12342347 RMVar_hsa_circ_6158,RMVar_hsa_circ_166465,RMVar_hsa_circ_268325,RMVar_hsa_circ_305972,RMVar_hsa_circ_354939,RMVar_hsa_circ_166469,RMVar_hsa_circ_21719,RMVar_hsa_circ_166470,RMVar_hsa_circ_316298,RMVar_hsa_circ_277163,RMVar_hsa_circ_166473,RMVar_hsa_circ_166474,RMVar_hsa_circ_292959,RMVar_hsa_circ_166477,RMVar_hsa_circ_166476,RMVar_hsa_circ_378207,RMVar_hsa_circ_166475,RMVar_hsa_circ_342364,RMVar_hsa_circ_362350,RMVar_hsa_circ_166478,RMVar_hsa_circ_303897 41615 RMVar_ID_41615 Human_SNP_ID_554815552 A-to-I Human chr14 - 50306878 50306878 50306878 CTGGGAGTGGGAAGCTGCAGTGAGCCGAGATCATGCTGCTACACTCCAACCTAGGCAATAGAGTG CTGGGAGTGGGAAGCTGCAGTGAGCCGAGATCGTGCTGCTACACTCCAACCTAGGCAATAGAGTG T C L2HGDH Ensembl:ENSG00000087299 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1243275447 Functional Loss SNV dbSNP153 33..33 33 - - - 41616 RMVar_ID_41616 Human_SNP_ID_554816137 A-to-I Human chr14 - 50309151 50309151 50309151 AGAAAAAAATTGACAAAATGGACTTCATCAAAATGAAAAACTTTTGCTCTGCAAAAGACTGTTAA AGAAAAAAATTGACAAAATGGACTTCATCAAAGTGAAAAACTTTTGCTCTGCAAAAGACTGTTAA T C L2HGDH Ensembl:ENSG00000087299 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs895033452 Functional Loss SNV dbSNP153 33..33 33 - - - 41617 RMVar_ID_41617 Human_SNP_ID_554816144 A-to-I Human chr14 - 50309183 50309182 50309184 ATAGAGATGACATCAAAAGCATGATCTCTAAAAGAAAAAAATTGACAAAATGGACTTCATCAAAA ATAGAGATGACATCAAAAGCATGATCTCTAA__GAAAAAAATTGACAAAATGGACTTCATCAAAA CTT C L2HGDH Ensembl:ENSG00000087299 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053669432 Functional Loss DEL dbSNP153 32..33 33 - - - 41618 RMVar_ID_41618 Human_SNP_ID_554816154 A-to-I Human chr14 - 50309215 50309215 50309215 AAACTTTTAGAAAAAGGACAAGATCTTTGGACATAGAGATGACATCAAAAGCATGATCTCTAAAA AAACTTTTAGAAAAAGGACAAGATCTTTGGACGTAGAGATGACATCAAAAGCATGATCTCTAAAA T C L2HGDH Ensembl:ENSG00000087299 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1235347709 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12342497 41619 RMVar_ID_41619 Human_SNP_ID_554820840 A-to-I Human chr14 + 50326069 50326067 50326069 CATGGCCAACATGGTGAAACCCCATCTCTACTAAAAAAACAAAATTAGCTGAATGTGGTGGTGCA CATGGCCAACATGGTGAAACCCCATCTCTAC__AAAAAACAAAATTAGCTGAATGTGGTGGTGCA CTA C DMAC2L Ensembl:ENSG00000125375 Protein coding exon GSE47997;GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line - 23474544,24183664,31158229 RNA-Seq:(High) rs1166851747 Functional Loss DEL dbSNP153 32..33 33 - - - 41620 RMVar_ID_41620 Human_SNP_ID_554820840 A-to-I Human chr14 - 50326068 50326067 50326069 GCACCACCACATTCAGCTAATTTTGTTTTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCATGG GCACCACCACATTCAGCTAATTTTGTTTTTT__GTAGAGATGGGGTTTCACCATGTTGGCCATGG CTA C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1166851747 Functional Loss DEL dbSNP153 32..33 33 - - - 41621 RMVar_ID_41621 Human_SNP_ID_554820842 A-to-I Human chr14 + 50326072 50326068 50326072 GGCCAACATGGTGAAACCCCATCTCTACTAAAAAAACAAAATTAGCTGAATGTGGTGGTGCACGC GGCCAACATGGTGAAACCCCATCTCTACT____AAACAAAATTAGCTGAATGTGGTGGTGCACGC TAAAA T DMAC2L Ensembl:ENSG00000125375 Protein coding exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1460898774 Functional Loss DEL dbSNP153 30..33 33 - - - 41622 RMVar_ID_41622 Human_SNP_ID_554820842 A-to-I Human chr14 + 50326071 50326068 50326072 TGGCCAACATGGTGAAACCCCATCTCTACTAAAAAAACAAAATTAGCTGAATGTGGTGGTGCACG TGGCCAACATGGTGAAACCCCATCTCTACT____AAACAAAATTAGCTGAATGTGGTGGTGCACG TAAAA T DMAC2L Ensembl:ENSG00000125375 Protein coding exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1460898774 Functional Loss DEL dbSNP153 31..34 33 - - - 41623 RMVar_ID_41623 Human_SNP_ID_554820843 A-to-I Human chr14 + 50326069 50326069 50326069 CATGGCCAACATGGTGAAACCCCATCTCTACTAAAAAAACAAAATTAGCTGAATGTGGTGGTGCA CATGGCCAACATGGTGAAACCCCATCTCTACTGAAAAAACAAAATTAGCTGAATGTGGTGGTGCA A G DMAC2L Ensembl:ENSG00000125375 Protein coding exon GSE47997;GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line - 23474544,24183664,31158229 RNA-Seq:(High) rs1029081777 Functional Loss SNV dbSNP153 33..33 33 - - - 41624 RMVar_ID_41624 Human_SNP_ID_554820844 A-to-I Human chr14 + 50326069 50326069 50326069 CATGGCCAACATGGTGAAACCCCATCTCTACTAAAAAAACAAAATTAGCTGAATGTGGTGGTGCA CATGGCCAACATGGTGAAACCCCATCTCTACTTAAAAAACAAAATTAGCTGAATGTGGTGGTGCA A T DMAC2L Ensembl:ENSG00000125375 Protein coding exon GSE47997;GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line - 23474544,24183664,31158229 RNA-Seq:(High) rs1029081777 Functional Loss SNV dbSNP153 33..33 33 - - - 41625 RMVar_ID_41625 Human_SNP_ID_554820848 A-to-I Human chr14 + 50326079 50326079 50326079 ATGGTGAAACCCCATCTCTACTAAAAAAACAAAATTAGCTGAATGTGGTGGTGCACGCCTTTAAT ATGGTGAAACCCCATCTCTACTAAAAAAACAAGATTAGCTGAATGTGGTGGTGCACGCCTTTAAT A G DMAC2L Ensembl:ENSG00000125375 Protein coding exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1480280140 Functional Loss SNV dbSNP153 33..33 33 - - - 41626 RMVar_ID_41626 Human_SNP_ID_554820857 A-to-I Human chr14 - 50326108 50326108 50326108 CTCCTGCCTCAGCCTCCAGAGTAGCTGGGATTAAAGGCGTGCACCACCACATTCAGCTAATTTTG CTCCTGCCTCAGCCTCCAGAGTAGCTGGGATTGAAGGCGTGCACCACCACATTCAGCTAATTTTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264852948 Functional Loss SNV dbSNP153 33..33 33 - - - 41627 RMVar_ID_41627 Human_SNP_ID_554820858 A-to-I Human chr14 + 50326115 50326114 50326115 AGCTGAATGTGGTGGTGCACGCCTTTAATCCCAGCTACTCTGGAGGCTGAGGCAGGAGAATCACT AGCTGAATGTGGTGGTGCACGCCTTTAATCCC_GCTACTCTGGAGGCTGAGGCAGGAGAATCACT CA C DMAC2L Ensembl:ENSG00000125375 Protein coding exon GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs895156727 Functional Loss DEL dbSNP153 33..33 33 - - - 41628 RMVar_ID_41628 Human_SNP_ID_554820859 A-to-I Human chr14 + 50326115 50326115 50326115 AGCTGAATGTGGTGGTGCACGCCTTTAATCCCAGCTACTCTGGAGGCTGAGGCAGGAGAATCACT AGCTGAATGTGGTGGTGCACGCCTTTAATCCCGGCTACTCTGGAGGCTGAGGCAGGAGAATCACT A G DMAC2L Ensembl:ENSG00000125375 Protein coding exon GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1566563726 Functional Loss SNV dbSNP153 33..33 33 - - - 41629 RMVar_ID_41629 Human_SNP_ID_554820866 A-to-I Human chr14 - 50326160 50326160 50326160 CAGTGGCACAATCTCGGGTCCCTGCAACCTCCACCTCCCAAGTCAAGTGATTCTCCTGCCTCAGC CAGTGGCACAATCTCGGGTCCCTGCAACCTCCGCCTCCCAAGTCAAGTGATTCTCCTGCCTCAGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1336038194 Functional Loss SNV dbSNP153 33..33 33 - - - 41630 RMVar_ID_41630 Human_SNP_ID_554821044 A-to-I Human chr14 + 50326894 50326894 50326894 GAGACCCCATCTCTAAAAAAATTTTAAAAATTAGGCAGGCATGGTGGTGCATACCTGTAATCTCA GAGACCCCATCTCTAAAAAAATTTTAAAAATTGGGCAGGCATGGTGGTGCATACCTGTAATCTCA A G DMAC2L Ensembl:ENSG00000125375 Protein coding exon GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs958904500 Functional Loss SNV dbSNP153 33..33 33 - - - 41631 RMVar_ID_41631 Human_SNP_ID_554821101 A-to-I Human chr14 + 50327184 50327184 50327184 ACCCTGTCTCTACCAAAAAATTAAAAAATAAAAAATAGCTGGGTGTAGTGGCACATGCCTGTAGT ACCCTGTCTCTACCAAAAAATTAAAAAATAAATAATAGCTGGGTGTAGTGGCACATGCCTGTAGT A T DMAC2L Ensembl:ENSG00000125375 Protein coding exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1344039760 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17849008 41632 RMVar_ID_41632 Human_SNP_ID_554821114 A-to-I Human chr14 + 50327214 50327214 50327214 AAAAATAGCTGGGTGTAGTGGCACATGCCTGTAGTCCCAACTACTCAGGAGTCTGAGGTAGGAGG AAAAATAGCTGGGTGTAGTGGCACATGCCTGTGGTCCCAACTACTCAGGAGTCTGAGGTAGGAGG A G DMAC2L Ensembl:ENSG00000125375 Protein coding exon GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1379741991 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12342670 41633 RMVar_ID_41633 Human_SNP_ID_554821118 A-to-I Human chr14 - 50327240 50327240 50327240 GCCTCGACTTCCCGGGCTCAACTGATCCTCCTACCTCAGACTCCTGAGTAGTTGGGACTACAGGC GCCTCGACTTCCCGGGCTCAACTGATCCTCCTCCCTCAGACTCCTGAGTAGTTGGGACTACAGGC T G AL359397.2 Ensembl:ENSG00000259071 lincRNA intron GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 29129909,30559470 RNA-Seq:(High) rs909285868 Functional Loss SNV dbSNP153 33..33 33 - - - 41634 RMVar_ID_41634 Human_SNP_ID_554821131 A-to-I Human chr14 - 50327320 50327320 50327320 ACTTTTTTTTTTTTTTTTGAGACAGGGTCTTAATCTGTTGCCCAGGCTGGAGTGCAGTGGTGCCA ACTTTTTTTTTTTTTTTTGAGACAGGGTCTTACTCTGTTGCCCAGGCTGGAGTGCAGTGGTGCCA T G AL359397.2 Ensembl:ENSG00000259071 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1469321269 Functional Loss SNV dbSNP153 33..33 33 - - - 41635 RMVar_ID_41635 Human_SNP_ID_554821257 A-to-I Human chr14 + 50327662 50327662 50327662 AATTTTTGTACTTTTAGTAGAGACAGGGTTTCACCATCTTGGCCAGACTGGTCTTGAACTCCTAA AATTTTTGTACTTTTAGTAGAGACAGGGTTTCGCCATCTTGGCCAGACTGGTCTTGAACTCCTAA A G DMAC2L Ensembl:ENSG00000125375 Protein coding exon GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1180438317 Functional Loss SNV dbSNP153 33..33 33 - - - 41636 RMVar_ID_41636 Human_SNP_ID_554821267 A-to-I Human chr14 + 50327706 50327706 50327706 AGACTGGTCTTGAACTCCTAACCTCAGGATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGAGCCA AGACTGGTCTTGAACTCCTAACCTCAGGATCCCCCCGCCTCGGCCTCCCAAAGTGCTGGGAGCCA A C DMAC2L Ensembl:ENSG00000125375 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs921287373 Functional Loss SNV dbSNP153 33..33 33 - - - 41637 RMVar_ID_41637 Human_SNP_ID_554821500 A-to-I Human chr14 + 50328765 50328765 50328765 TAATGCCAGCACTTTGGAAGGCCAAGGCGCTCAGATCACGTGAGCCCAGGAGTTCAAGACCAGCC TAATGCCAGCACTTTGGAAGGCCAAGGCGCTCGGATCACGTGAGCCCAGGAGTTCAAGACCAGCC A G DMAC2L Ensembl:ENSG00000125375 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1238079785 Functional Loss SNV dbSNP153 33..33 33 - - - 41638 RMVar_ID_41638 Human_SNP_ID_554835174 A-to-I Human chr14 - 50383367 50383367 50383367 TTTTGTATTTTTAGTGGAGGTAGGGTTTCACCATATTGGCCCGGCTGGTCTCGAACTCCTGACCT TTTTGTATTTTTAGTGGAGGTAGGGTTTCACCGTATTGGCCCGGCTGGTCTCGAACTCCTGACCT T C CDKL1 Ensembl:ENSG00000100490 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs912254723 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28560,RMVar_hsa_circ_166489,RMVar_hsa_circ_102595 41639 RMVar_ID_41639 Human_SNP_ID_554837864 A-to-I Human chr14 - 50393589 50393588 50393589 GGTCCTAGCTACTAAGGAAAGAGGCCAAGGCAAGAGGATGGCTTAAGCCCAGCAGTTCAAGGCTA GGTCCTAGCTACTAAGGAAAGAGGCCAAGGCA_GAGGATGGCTTAAGCCCAGCAGTTCAAGGCTA CT C CDKL1 Ensembl:ENSG00000100490 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1286372345 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_28560,RMVar_hsa_circ_166489,RMVar_hsa_circ_102595 41640 RMVar_ID_41640 Human_SNP_ID_554842845 A-to-I Human chr14 - 50414073 50414073 50414073 CGCCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACTGCGCCCGGCCAGGAAGT CGCCCGCCTCAGCCTCCCAAAGTGCTGGGATTTCAGGTGTGAGCCACTGCGCCCGGCCAGGAAGT T A CDKL1 Ensembl:ENSG00000100490 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs958753201 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_166491 41641 RMVar_ID_41641 Human_SNP_ID_554842973 A-to-I Human chr14 - 50414272 50414270 50414272 CAGGCTGGAGTGCAGTGGCGCGATCTCGGCTCACTGCGAGCTCCGCCTCCTGGTTCACGCCATTC CAGGCTGGAGTGCAGTGGCGCGATCTCGGCTC__TGCGAGCTCCGCCTCCTGGTTCACGCCATTC AGT A CDKL1 Ensembl:ENSG00000100490 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1464887269 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_166491 41642 RMVar_ID_41642 Human_SNP_ID_554859396 A-to-I Human chr14 - 50483928 50483928 50483928 TGCACCCAGGAGGCGGTGGTTGCAGTGAACCAAGATCACGCCAGTGCACTCCAGCCTGGGCGAGA TGCACCCAGGAGGCGGTGGTTGCAGTGAACCAGGATCACGCCAGTGCACTCCAGCCTGGGCGAGA T C MAP4K5 Ensembl:ENSG00000012983 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1414814707 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_446619,Human_RBP_ID_12343869 RMVar_hsa_circ_166496,RMVar_hsa_circ_2345,RMVar_hsa_circ_16958,RMVar_hsa_circ_267947,RMVar_hsa_circ_319585,RMVar_hsa_circ_44823,RMVar_hsa_circ_275890,RMVar_hsa_circ_166509,RMVar_hsa_circ_328481,RMVar_hsa_circ_295732,RMVar_hsa_circ_40597,RMVar_hsa_circ_166517,RMVar_hsa_circ_166518,RMVar_hsa_circ_166526,RMVar_hsa_circ_12996,RMVar_hsa_circ_336203,RMVar_hsa_circ_293226,RMVar_hsa_circ_166519,RMVar_hsa_circ_307910,RMVar_hsa_circ_299467,RMVar_hsa_circ_113548,RMVar_hsa_circ_119320,RMVar_hsa_circ_166527,RMVar_hsa_circ_166528,RMVar_hsa_circ_166529,RMVar_hsa_circ_166525,RMVar_hsa_circ_314207,RMVar_hsa_circ_166532,RMVar_hsa_circ_271139,RMVar_hsa_circ_342926,RMVar_hsa_circ_166533 41643 RMVar_ID_41643 Human_SNP_ID_554861289 A-to-I Human chr14 - 50491791 50491791 50491791 ATCCCAGCTACTTAGGAGGCTGAGGTGGGAGAATTGCTTGAGCCCAGGAGGTTGAGGCTGCAGTG ATCCCAGCTACTTAGGAGGCTGAGGTGGGAGATTTGCTTGAGCCCAGGAGGTTGAGGCTGCAGTG T A MAP4K5 Ensembl:ENSG00000012983 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs979619152 Functional Loss SNV dbSNP153 33..33 33 - - - 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 41644 RMVar_ID_41644 Human_SNP_ID_554861621 A-to-I Human chr14 - 50493197 50493197 50493197 TACCTGGGAGGCTGAGGCAGAAGGACTGCTTGAGCCCAGGAGTTTGAGGCTGCAGTGAGCAATGA TACCTGGGAGGCTGAGGCAGAAGGACTGCTTGTGCCCAGGAGTTTGAGGCTGCAGTGAGCAATGA T A MAP4K5 Ensembl:ENSG00000012983 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904614753 Functional Loss SNV dbSNP153 33..33 33 - - - 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 41645 RMVar_ID_41645 Human_SNP_ID_554893909 A-to-I Human chr14 - 50634505 50634505 50634505 CTCTACAAAAAATACAAAAAAATTAGCCGGGTATGATGGTGTGTGCCTCTAGTCCCAGCTACTTG CTCTACAAAAAATACAAAAAAATTAGCCGGGTGTGATGGTGTGTGCCTCTAGTCCCAGCTACTTG T C SAV1 Ensembl:ENSG00000151748 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1216593287 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_446692 41646 RMVar_ID_41646 Human_SNP_ID_554920196 A-to-I Human chr14 - 50725659 50725659 50725659 GGACCTAAGATTTTAAAGATCAAAAAAAATCTATTGATTCACATAGACCTAAAGCATGTCCATTC GGACCTAAGATTTTAAAGATCAAAAAAAATCTGTTGATTCACATAGACCTAAAGCATGTCCATTC T C NIN Ensembl:ENSG00000100503 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1166146538 Functional Loss SNV dbSNP153 33..33 33 - - - 41647 RMVar_ID_41647 Human_SNP_ID_554925041 A-to-I Human chr14 - 50742273 50742273 50742273 CCAGGTAGTTGGGACTACAGGCACACGCCACCACACTCAGCTTTTTATTTTTGGTAGAGATGGGG CCAGGTAGTTGGGACTACAGGCACACGCCACCGCACTCAGCTTTTTATTTTTGGTAGAGATGGGG T C NIN Ensembl:ENSG00000100503 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1050301003 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6516,RMVar_hsa_circ_166555,RMVar_hsa_circ_301170,RMVar_hsa_circ_303676,RMVar_hsa_circ_5197,RMVar_hsa_circ_166557,RMVar_hsa_circ_35034,RMVar_hsa_circ_314741,RMVar_hsa_circ_166556,RMVar_hsa_circ_324957,RMVar_hsa_circ_166558,RMVar_hsa_circ_324799,RMVar_hsa_circ_7821,RMVar_hsa_circ_49435,RMVar_hsa_circ_328480,RMVar_hsa_circ_283013,RMVar_hsa_circ_322869,RMVar_hsa_circ_13864,RMVar_hsa_circ_166562,RMVar_hsa_circ_166563,RMVar_hsa_circ_166564,RMVar_hsa_circ_166561 41648 RMVar_ID_41648 Human_SNP_ID_554926519 A-to-I Human chr14 - 50747738 50747734 50747738 TACACTCTAAAATCCCCCCCTTTTTTTTTTTTAAGACAGTTTCCTTCTTCCCTCTGTTGCCTAGG TACACTCTAAAATCCCCCCCTTTTTTTTTTTT____CAGTTTCCTTCTTCCCTCTGTTGCCTAGG GTCTT G NIN Ensembl:ENSG00000100503 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1160503339 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_6516,RMVar_hsa_circ_5197,RMVar_hsa_circ_166557,RMVar_hsa_circ_35034,RMVar_hsa_circ_314741,RMVar_hsa_circ_324799,RMVar_hsa_circ_7821,RMVar_hsa_circ_49435,RMVar_hsa_circ_322869,RMVar_hsa_circ_13864,RMVar_hsa_circ_64625,RMVar_hsa_circ_166563,RMVar_hsa_circ_166564,RMVar_hsa_circ_315198,RMVar_hsa_circ_355006,RMVar_hsa_circ_23643,RMVar_hsa_circ_166567,RMVar_hsa_circ_23989,RMVar_hsa_circ_166568 41649 RMVar_ID_41649 Human_SNP_ID_554926526 A-to-I Human chr14 - 50747738 50747738 50747738 TACACTCTAAAATCCCCCCCTTTTTTTTTTTTAAGACAGTTTCCTTCTTCCCTCTGTTGCCTAGG TACACTCTAAAATCCCCCCCTTTTTTTTTTTTTAGACAGTTTCCTTCTTCCCTCTGTTGCCTAGG T A NIN Ensembl:ENSG00000100503 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1261620438 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6516,RMVar_hsa_circ_5197,RMVar_hsa_circ_166557,RMVar_hsa_circ_35034,RMVar_hsa_circ_314741,RMVar_hsa_circ_324799,RMVar_hsa_circ_7821,RMVar_hsa_circ_49435,RMVar_hsa_circ_322869,RMVar_hsa_circ_13864,RMVar_hsa_circ_64625,RMVar_hsa_circ_166563,RMVar_hsa_circ_166564,RMVar_hsa_circ_315198,RMVar_hsa_circ_355006,RMVar_hsa_circ_23643,RMVar_hsa_circ_166567,RMVar_hsa_circ_23989,RMVar_hsa_circ_166568 41650 RMVar_ID_41650 Human_SNP_ID_554926527 A-to-I Human chr14 - 50747738 50747738 50747738 TACACTCTAAAATCCCCCCCTTTTTTTTTTTTAAGACAGTTTCCTTCTTCCCTCTGTTGCCTAGG TACACTCTAAAATCCCCCCCTTTTTTTTTTTTGAGACAGTTTCCTTCTTCCCTCTGTTGCCTAGG T C NIN Ensembl:ENSG00000100503 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1261620438 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6516,RMVar_hsa_circ_5197,RMVar_hsa_circ_166557,RMVar_hsa_circ_35034,RMVar_hsa_circ_314741,RMVar_hsa_circ_324799,RMVar_hsa_circ_7821,RMVar_hsa_circ_49435,RMVar_hsa_circ_322869,RMVar_hsa_circ_13864,RMVar_hsa_circ_64625,RMVar_hsa_circ_166563,RMVar_hsa_circ_166564,RMVar_hsa_circ_315198,RMVar_hsa_circ_355006,RMVar_hsa_circ_23643,RMVar_hsa_circ_166567,RMVar_hsa_circ_23989,RMVar_hsa_circ_166568 41651 RMVar_ID_41651 Human_SNP_ID_554939855 A-to-I Human chr14 - 50799936 50799936 50799936 AGTTTTGCTCTTGTTGCCCAAGCTGGAATGCAATGGTGCAATCTCGGCTCACTGCAACCTCTGCC AGTTTTGCTCTTGTTGCCCAAGCTGGAATGCAGTGGTGCAATCTCGGCTCACTGCAACCTCTGCC T C NIN Ensembl:ENSG00000100503 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1332808773 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_46869,RMVar_hsa_circ_266035,RMVar_hsa_circ_265903,RMVar_hsa_circ_73084,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_166582 41652 RMVar_ID_41652 Human_SNP_ID_554944282 A-to-I Human chr14 - 50817844 50817844 50817844 CGGCGTGGCAGTGGGCGCCGGTAATCCTAGCTACTCGGGAGGCTGAGACAGGAGAATTGCTTGAA CGGCGTGGCAGTGGGCGCCGGTAATCCTAGCTGCTCGGGAGGCTGAGACAGGAGAATTGCTTGAA T C NIN Ensembl:ENSG00000100503 Protein coding intron GSE38233;GSE107867 cultured B-cells;ASD brains,frontal_cortex - 24183664,30559470 RNA-Seq:(High) rs1166836588 Functional Loss SNV dbSNP153 33..33 33 - - - 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_308919 41653 RMVar_ID_41653 Human_SNP_ID_554974332 A-to-I Human chr14 - 50933693 50933693 50933693 TAGAAAAAAAGGTCTGGAATTTTAAATACGAAACTGTTCCCTACGACCCCCTGTAGGGAGGAGTG TAGAAAAAAAGGTCTGGAATTTTAAATACGAAGCTGTTCCCTACGACCCCCTGTAGGGAGGAGTG T C PYGL Ensembl:ENSG00000100504 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs12882737 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_358622,RMVar_hsa_circ_29172,RMVar_hsa_circ_11710,RMVar_hsa_circ_120992,RMVar_hsa_circ_166595 41654 RMVar_ID_41654 Human_SNP_ID_554974333 A-to-I Human chr14 - 50933695 50933695 50933695 TGTAGAAAAAAAGGTCTGGAATTTTAAATACGAAACTGTTCCCTACGACCCCCTGTAGGGAGGAG TGTAGAAAAAAAGGTCTGGAATTTTAAATACGTAACTGTTCCCTACGACCCCCTGTAGGGAGGAG T A PYGL Ensembl:ENSG00000100504 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs12882739 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_358622,RMVar_hsa_circ_29172,RMVar_hsa_circ_11710,RMVar_hsa_circ_120992,RMVar_hsa_circ_166595 41655 RMVar_ID_41655 Human_SNP_ID_554974337 A-to-I Human chr14 - 50933701 50933701 50933701 TGAATATGTAGAAAAAAAGGTCTGGAATTTTAAATACGAAACTGTTCCCTACGACCCCCTGTAGG TGAATATGTAGAAAAAAAGGTCTGGAATTTTACATACGAAACTGTTCCCTACGACCCCCTGTAGG T G PYGL Ensembl:ENSG00000100504 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs12882740 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_358622,RMVar_hsa_circ_29172,RMVar_hsa_circ_11710,RMVar_hsa_circ_120992,RMVar_hsa_circ_166595 41656 RMVar_ID_41656 Human_SNP_ID_554974343 A-to-I Human chr14 - 50933716 50933715 50933716 CATATGTATATAATGTGAATATGTAGAAAAAAAGGTCTGGAATTTTAAATACGAAACTGTTCCCT CATATGTATATAATGTGAATATGTAGAAAAAA_GGTCTGGAATTTTAAATACGAAACTGTTCCCT CT C PYGL Ensembl:ENSG00000100504 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1281119412 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_358622,RMVar_hsa_circ_29172,RMVar_hsa_circ_11710,RMVar_hsa_circ_120992,RMVar_hsa_circ_166595 41657 RMVar_ID_41657 Human_SNP_ID_554974346 A-to-I Human chr14 - 50933728 50933728 50933728 TGTGTGTGTGTACATATGTATATAATGTGAATATGTAGAAAAAAAGGTCTGGAATTTTAAATACG TGTGTGTGTGTACATATGTATATAATGTGAATGTGTAGAAAAAAAGGTCTGGAATTTTAAATACG T C PYGL Ensembl:ENSG00000100504 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042986650 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_358622,RMVar_hsa_circ_29172,RMVar_hsa_circ_11710,RMVar_hsa_circ_120992,RMVar_hsa_circ_166595 41658 RMVar_ID_41658 Human_SNP_ID_554974405 A-to-I Human chr14 - 50933918 50933918 50933918 CCTAGCTAGATCTCCAAATTAAAAGCGAAATCAAATTGCATTAAAGCCATACAGTGTGATACCAT CCTAGCTAGATCTCCAAATTAAAAGCGAAATCTAATTGCATTAAAGCCATACAGTGTGATACCAT T A PYGL Ensembl:ENSG00000100504 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167670870 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_358622,RMVar_hsa_circ_29172,RMVar_hsa_circ_11710,RMVar_hsa_circ_120992,RMVar_hsa_circ_166595 41659 RMVar_ID_41659 Human_SNP_ID_554989127 A-to-I Human chr14 - 50990245 50990245 50990245 GGGAGGCTGAGGTGGGAGGACTGCTTGAGGCCAGTGGTTTGAGACCAGCCTGGGCAACATAAAAA GGGAGGCTGAGGTGGGAGGACTGCTTGAGGCCGGTGGTTTGAGACCAGCCTGGGCAACATAAAAA T C TRIM9 Ensembl:ENSG00000100505 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1452902102 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42344 41660 RMVar_ID_41660 Human_SNP_ID_554989624 A-to-I Human chr14 - 50992437 50992437 50992437 TCCCTAGTAACTGGCTCTATAGGCATGCCACCACACCTGGCTTTTTTTTTTTTCCGTAGAGACAG TCCCTAGTAACTGGCTCTATAGGCATGCCACCCCACCTGGCTTTTTTTTTTTTCCGTAGAGACAG T G TRIM9 Ensembl:ENSG00000100505 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1334700600 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42344 41661 RMVar_ID_41661 Human_SNP_ID_554989629 A-to-I Human chr14 - 50992461 50992461 50992461 TCAAGTGATCCTCCTGCCTCAGCCTCCCTAGTAACTGGCTCTATAGGCATGCCACCACACCTGGC TCAAGTGATCCTCCTGCCTCAGCCTCCCTAGTGACTGGCTCTATAGGCATGCCACCACACCTGGC T C TRIM9 Ensembl:ENSG00000100505 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1202568018 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42344 41662 RMVar_ID_41662 Human_SNP_ID_554989634 A-to-I Human chr14 - 50992490 50992490 50992490 TGGCTCACTGTAACCTTGACCTCCTGGGCTCAAGTGATCCTCCTGCCTCAGCCTCCCTAGTAACT TGGCTCACTGTAACCTTGACCTCCTGGGCTCAGGTGATCCTCCTGCCTCAGCCTCCCTAGTAACT T C TRIM9 Ensembl:ENSG00000100505 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs776428307 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42344 41663 RMVar_ID_41663 Human_SNP_ID_554990082 A-to-I Human chr14 - 50994400 50994400 50994400 CTGACCTTTCTACCTTCCTTTTTTTTGAGACAAGGTCACACTCTGTCACCCAGGCTGCAGTGCAG CTGACCTTTCTACCTTCCTTTTTTTTGAGACAGGGTCACACTCTGTCACCCAGGCTGCAGTGCAG T C TRIM9 Ensembl:ENSG00000100505 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs554741769 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42344 41664 RMVar_ID_41664 Human_SNP_ID_555142666 A-to-I Human chr14 - 51642280 51642280 51642280 CCACCTTGGCCTCCCAAAGTGCTGGGATTACAAGCGTGAGCCACCATGCCCGGCCTCTGGCCTCC CCACCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCATGCCCGGCCTCTGGCCTCC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs936841991 Functional Loss SNV dbSNP153 33..33 33 - - - 41665 RMVar_ID_41665 Human_SNP_ID_555146883 A-to-I Human chr14 + 51658222 51658222 51658222 ATGGCTCTGTTCAGATAGACTCAGATCTGCCCAGAGGAAATGGATCTGTAGCCCAATGAGGCAGA ATGGCTCTGTTCAGATAGACTCAGATCTGCCCGGAGGAAATGGATCTGTAGCCCAATGAGGCAGA A G FRMD6 Ensembl:ENSG00000139926 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1489519814 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86907,RMVar_hsa_circ_122659,RMVar_hsa_circ_102090,RMVar_hsa_circ_166612,RMVar_hsa_circ_166613,RMVar_hsa_circ_166614 41666 RMVar_ID_41666 Human_SNP_ID_555303536 A-to-I Human chr14 + 52273056 52273056 52273056 TTTTTTGAGACAGTGTTTCACTCTTGTCACCCAGGCTGGAGTACAATGGCACAATCTAGGCGCAC TTTTTTGAGACAGTGTTTCACTCTTGTCACCCTGGCTGGAGTACAATGGCACAATCTAGGCGCAC A T PTGDR Ensembl:ENSG00000168229 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs983281036 Functional Loss SNV dbSNP153 33..33 33 - - - 41667 RMVar_ID_41667 Human_SNP_ID_555356665 A-to-I Human chr14 - 52496758 52496758 52496758 AAAAACATAAAAAATTAGCTGGGTATGATGGTATGCACCTGTAGTCCCAGCTACTTGGGAGGCTG AAAAACATAAAAAATTAGCTGGGTATGATGGTGTGCACCTGTAGTCCCAGCTACTTGGGAGGCTG T C TXNDC16 Ensembl:ENSG00000087301 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971059524 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4177,RMVar_hsa_circ_8699,RMVar_hsa_circ_80295,RMVar_hsa_circ_166655,RMVar_hsa_circ_166656,RMVar_hsa_circ_296227,RMVar_hsa_circ_333038,RMVar_hsa_circ_40620,RMVar_hsa_circ_318280,RMVar_hsa_circ_21240,RMVar_hsa_circ_18741,RMVar_hsa_circ_166668,RMVar_hsa_circ_166673,RMVar_hsa_circ_275814,RMVar_hsa_circ_346093,RMVar_hsa_circ_288379,RMVar_hsa_circ_166679,RMVar_hsa_circ_166678,RMVar_hsa_circ_43655,RMVar_hsa_circ_7165,RMVar_hsa_circ_285829,RMVar_hsa_circ_71665,RMVar_hsa_circ_166680,RMVar_hsa_circ_316661,RMVar_hsa_circ_166683,RMVar_hsa_circ_333616,RMVar_hsa_circ_335026,RMVar_hsa_circ_326839,RMVar_hsa_circ_166685,RMVar_hsa_circ_30445 41668 RMVar_ID_41668 Human_SNP_ID_555356666 A-to-I Human chr14 - 52496766 52496766 52496766 ATCTCTACAAAAACATAAAAAATTAGCTGGGTATGATGGTATGCACCTGTAGTCCCAGCTACTTG ATCTCTACAAAAACATAAAAAATTAGCTGGGTGTGATGGTATGCACCTGTAGTCCCAGCTACTTG T C TXNDC16 Ensembl:ENSG00000087301 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1397130371 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4177,RMVar_hsa_circ_8699,RMVar_hsa_circ_80295,RMVar_hsa_circ_166655,RMVar_hsa_circ_166656,RMVar_hsa_circ_296227,RMVar_hsa_circ_333038,RMVar_hsa_circ_40620,RMVar_hsa_circ_318280,RMVar_hsa_circ_21240,RMVar_hsa_circ_18741,RMVar_hsa_circ_166668,RMVar_hsa_circ_166673,RMVar_hsa_circ_275814,RMVar_hsa_circ_346093,RMVar_hsa_circ_288379,RMVar_hsa_circ_166679,RMVar_hsa_circ_166678,RMVar_hsa_circ_43655,RMVar_hsa_circ_7165,RMVar_hsa_circ_285829,RMVar_hsa_circ_71665,RMVar_hsa_circ_166680,RMVar_hsa_circ_316661,RMVar_hsa_circ_166683,RMVar_hsa_circ_333616,RMVar_hsa_circ_335026,RMVar_hsa_circ_326839,RMVar_hsa_circ_166685,RMVar_hsa_circ_30445 41669 RMVar_ID_41669 Human_SNP_ID_555387606 A-to-I Human chr14 + 52612665 52612665 52612665 CTTACTGTAACCTCAAACTCCTGGGCTTATGTAATTCTCCTACCTCAGCCTCCCAAGTAGCTAGA CTTACTGTAACCTCAAACTCCTGGGCTTATGTGATTCTCCTACCTCAGCCTCCCAAGTAGCTAGA A G GPR137C Ensembl:ENSG00000180998 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs993432513 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_294060,RMVar_hsa_circ_166694 41670 RMVar_ID_41670 Human_SNP_ID_555387611 A-to-I Human chr14 + 52612695 52612695 52612695 GTAATTCTCCTACCTCAGCCTCCCAAGTAGCTAGAACTGCGAGCATTCACCACCACACTCAGCTT GTAATTCTCCTACCTCAGCCTCCCAAGTAGCTGGAACTGCGAGCATTCACCACCACACTCAGCTT A G GPR137C Ensembl:ENSG00000180998 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991206594 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_294060,RMVar_hsa_circ_166694 41671 RMVar_ID_41671 Human_SNP_ID_555387654 A-to-I Human chr14 + 52612827 52612827 52612827 GCCTCAGATGATCCTGTCATCTTGGCCTTCCAAAGTACTGGGATTACAAGCATGAGCCATGGTAC GCCTCAGATGATCCTGTCATCTTGGCCTTCCAGAGTACTGGGATTACAAGCATGAGCCATGGTAC A G GPR137C Ensembl:ENSG00000180998 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1248816802 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_294060,RMVar_hsa_circ_166694 41672 RMVar_ID_41672 Human_SNP_ID_555399806 A-to-I Human chr14 - 52665202 52665202 52665202 TGCCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCACACG TGCCTCCCAGGTTCAAGCGATTCTCCTGCCTCGGCCTCCTGAGTAGCTGGGACTACAGGCACACG T C ERO1A Ensembl:ENSG00000197930 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs760638389 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3785,RMVar_hsa_circ_305776,RMVar_hsa_circ_58052,RMVar_hsa_circ_298218,RMVar_hsa_circ_364618,RMVar_hsa_circ_166705,RMVar_hsa_circ_166707,RMVar_hsa_circ_292235,RMVar_hsa_circ_105987,RMVar_hsa_circ_31672,RMVar_hsa_circ_78157,RMVar_hsa_circ_166708,RMVar_hsa_circ_19422 41673 RMVar_ID_41673 Human_SNP_ID_555402704 A-to-I Human chr14 - 52677781 52677781 52677781 ATAGCTCACTGTAACCTTGAACTCCTGGGCTAAAGTGATTCTCTCCCCTCAGCTTTCCGAGTAGC ATAGCTCACTGTAACCTTGAACTCCTGGGCTAGAGTGATTCTCTCCCCTCAGCTTTCCGAGTAGC T C ERO1A Ensembl:ENSG00000197930 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991359631 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3785,RMVar_hsa_circ_1524,RMVar_hsa_circ_58052,RMVar_hsa_circ_166707,RMVar_hsa_circ_105987,RMVar_hsa_circ_31672,RMVar_hsa_circ_78157,RMVar_hsa_circ_166708,RMVar_hsa_circ_37530,RMVar_hsa_circ_372772,RMVar_hsa_circ_166709,RMVar_hsa_circ_166711,RMVar_hsa_circ_298139,RMVar_hsa_circ_318019,RMVar_hsa_circ_289489,RMVar_hsa_circ_166710 41674 RMVar_ID_41674 Human_SNP_ID_555411615 A-to-I Human chr14 + 52712692 52712692 52712692 TTGCCCAGGCTGGAATGCAGTGGTGCAGTCTCAGCTCACTGCAACCTCTACCTCCCAGGCTGAAG TTGCCCAGGCTGGAATGCAGTGGTGCAGTCTCGGCTCACTGCAACCTCTACCTCCCAGGCTGAAG A G PSMC6 Ensembl:ENSG00000100519 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs938291107 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_364,RMVar_hsa_circ_63724,RMVar_hsa_circ_3353,RMVar_hsa_circ_69753,RMVar_hsa_circ_1514,RMVar_hsa_circ_273442,RMVar_hsa_circ_293821,RMVar_hsa_circ_325888,RMVar_hsa_circ_127335,RMVar_hsa_circ_166718 41675 RMVar_ID_41675 Human_SNP_ID_555411644 A-to-I Human chr14 + 52712817 52712817 52712817 TTTTTTATTTTTTGTAGAGATGGGGTTTCACCATGTTGTCCAGGCTCTTCTCGAACTCCTGAACT TTTTTTATTTTTTGTAGAGATGGGGTTTCACCGTGTTGTCCAGGCTCTTCTCGAACTCCTGAACT A G PSMC6 Ensembl:ENSG00000100519 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1048448449 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_364,RMVar_hsa_circ_63724,RMVar_hsa_circ_3353,RMVar_hsa_circ_69753,RMVar_hsa_circ_1514,RMVar_hsa_circ_273442,RMVar_hsa_circ_293821,RMVar_hsa_circ_325888,RMVar_hsa_circ_127335,RMVar_hsa_circ_166718 41676 RMVar_ID_41676 Human_SNP_ID_555411717 A-to-I Human chr14 + 52713079 52713079 52713079 ACAGTGAAACCCCATCTCTTCTAAAAGTACAAAAATTAGCCAGGTGTGGTGGTGGCGCCTGTAGT ACAGTGAAACCCCATCTCTTCTAAAAGTACAACAATTAGCCAGGTGTGGTGGTGGCGCCTGTAGT A C PSMC6 Ensembl:ENSG00000100519 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1196388374 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_364,RMVar_hsa_circ_63724,RMVar_hsa_circ_3353,RMVar_hsa_circ_69753,RMVar_hsa_circ_1514,RMVar_hsa_circ_273442,RMVar_hsa_circ_293821,RMVar_hsa_circ_325888,RMVar_hsa_circ_127335,RMVar_hsa_circ_166718 41677 RMVar_ID_41677 Human_SNP_ID_555411985 A-to-I Human chr14 + 52714206 52714206 52714206 GGGACTGCAGGCGTGCATCACCATGTCTGGTTAATTTTTGTATGTTTTGTAGAGAAGCAATTTTG GGGACTGCAGGCGTGCATCACCATGTCTGGTTCATTTTTGTATGTTTTGTAGAGAAGCAATTTTG A C PSMC6 Ensembl:ENSG00000100519 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1243677499 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_364,RMVar_hsa_circ_3353,RMVar_hsa_circ_1514,RMVar_hsa_circ_273442,RMVar_hsa_circ_325888,RMVar_hsa_circ_127335,RMVar_hsa_circ_42611,RMVar_hsa_circ_166718 41678 RMVar_ID_41678 Human_SNP_ID_555412867 A-to-I Human chr14 + 52717762 52717762 52717762 CACATAGGCCGGGTGCGGTGGCTCCTGCCTGTAATCCCAGCACTTTGGGAGGCTGAAGTGGCAGG CACATAGGCCGGGTGCGGTGGCTCCTGCCTGTCATCCCAGCACTTTGGGAGGCTGAAGTGGCAGG A C PSMC6 Ensembl:ENSG00000100519 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1016918504 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_364,RMVar_hsa_circ_3353,RMVar_hsa_circ_1514,RMVar_hsa_circ_273442,RMVar_hsa_circ_325888,RMVar_hsa_circ_127335,RMVar_hsa_circ_42611,RMVar_hsa_circ_166718 41679 RMVar_ID_41679 Human_SNP_ID_555412894 A-to-I Human chr14 + 52717881 52717881 52717881 CTCTGAAAAACAAACAGACAAACAAAAAACTTAGCTGTGCGTGATGGCACATGCCTGTCATCCCA CTCTGAAAAACAAACAGACAAACAAAAAACTTCGCTGTGCGTGATGGCACATGCCTGTCATCCCA A C PSMC6 Ensembl:ENSG00000100519 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs945945504 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_364,RMVar_hsa_circ_3353,RMVar_hsa_circ_1514,RMVar_hsa_circ_273442,RMVar_hsa_circ_325888,RMVar_hsa_circ_127335,RMVar_hsa_circ_42611,RMVar_hsa_circ_166718 41680 RMVar_ID_41680 Human_SNP_ID_555413855 A-to-I Human chr14 + 52721545 52721545 52721545 AGTGGGGGGCGGGCATGGTGGCTCACTCCTGTAATCCTAATGGTTTTGGAGGCCGAGGCAGAAGG AGTGGGGGGCGGGCATGGTGGCTCACTCCTGTGATCCTAATGGTTTTGGAGGCCGAGGCAGAAGG A G PSMC6 Ensembl:ENSG00000100519 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1046327954 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3353,RMVar_hsa_circ_273442,RMVar_hsa_circ_42611,RMVar_hsa_circ_42151,RMVar_hsa_circ_35849 41681 RMVar_ID_41681 Human_SNP_ID_555419592 A-to-I Human chr14 + 52743460 52743460 52743460 AAAAAAATTATGGCGTGGTGGTGGGTGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAAAAATTATGGCGTGGTGGTGGGTGCCTGTGGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA A G STYX Ensembl:ENSG00000198252 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs967346055 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110699,RMVar_hsa_circ_120869,RMVar_hsa_circ_166719,RMVar_hsa_circ_166720 41682 RMVar_ID_41682 Human_SNP_ID_555427547 A-to-I Human chr14 - 52775658 52775658 52775658 CAAACTCCTGAGCTCAAGTGATCCTCTGCCTCAGCCTCCAGAGTATCTGGGATTACATATGTCGG CAAACTCCTGAGCTCAAGTGATCCTCTGCCTCCGCCTCCAGAGTATCTGGGATTACATATGTCGG T G GNPNAT1 Ensembl:ENSG00000100522 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs925687890 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6356547,Human_RBP_ID_12350940,Human_RBP_ID_27431547 Human_miRNA_ID_1394736,Human_miRNA_ID_2715171,Human_miRNA_ID_2784305,Human_miRNA_ID_3051153 RMVar_hsa_circ_124161,RMVar_hsa_circ_166733,RMVar_hsa_circ_113990,RMVar_hsa_circ_117524,RMVar_hsa_circ_166734,RMVar_hsa_circ_166735 41683 RMVar_ID_41683 Human_SNP_ID_555427553 A-to-I Human chr14 - 52775688 52775688 52775688 GGGGTCTTACTATATTGCCCAAGCCGGTCTCAAACTCCTGAGCTCAAGTGATCCTCTGCCTCAGC GGGGTCTTACTATATTGCCCAAGCCGGTCTCAGACTCCTGAGCTCAAGTGATCCTCTGCCTCAGC T C GNPNAT1 Ensembl:ENSG00000100522 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388208769 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12350940,Human_RBP_ID_26431997,Human_RBP_ID_27431547 RMVar_hsa_circ_124161,RMVar_hsa_circ_166733,RMVar_hsa_circ_113990,RMVar_hsa_circ_117524,RMVar_hsa_circ_166734,RMVar_hsa_circ_166735 41684 RMVar_ID_41684 Human_SNP_ID_555427570 A-to-I Human chr14 - 52775782 52775782 52775782 AGTTCCTGGGTTCAAGCCATCCCTCCTGCCTCAGCCTCCCCAGTAGCTGGAACTACAGGTGTGTG AGTTCCTGGGTTCAAGCCATCCCTCCTGCCTCCGCCTCCCCAGTAGCTGGAACTACAGGTGTGTG T G GNPNAT1 Ensembl:ENSG00000100522 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-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 41685 RMVar_ID_41685 Human_SNP_ID_555427579 A-to-I Human chr14 - 52775826 52775826 52775826 CAGGCTGGAGTCCAGTGGTGTGATCATAGCTCACTGCATCCTCCAGTTCCTGGGTTCAAGCCATC CAGGCTGGAGTCCAGTGGTGTGATCATAGCTCGCTGCATCCTCCAGTTCCTGGGTTCAAGCCATC T C GNPNAT1 Ensembl:ENSG00000100522 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1419417902 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6356550,Human_RBP_ID_17479310 Human_miRNA_ID_2466935,Human_miRNA_ID_3088589 RMVar_hsa_circ_124161,RMVar_hsa_circ_166733,RMVar_hsa_circ_113990,RMVar_hsa_circ_117524,RMVar_hsa_circ_166734,RMVar_hsa_circ_166735 41686 RMVar_ID_41686 Human_SNP_ID_555427653 A-to-I Human chr14 - 52776088 52776088 52776088 CACACACTGCCGCTTCAATCTCCTGGGCTCAAATGATCCTTCCACCTCAGCCTCCCATGTGGCTG CACACACTGCCGCTTCAATCTCCTGGGCTCAAGTGATCCTTCCACCTCAGCCTCCCATGTGGCTG T C GNPNAT1 Ensembl:ENSG00000100522 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1268558268 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8181432,Human_RBP_ID_23160970 RMVar_hsa_circ_124161,RMVar_hsa_circ_166733,RMVar_hsa_circ_113990,RMVar_hsa_circ_117524,RMVar_hsa_circ_166734,RMVar_hsa_circ_166735 41687 RMVar_ID_41687 Human_SNP_ID_555427821 A-to-I Human chr14 - 52776716 52776716 52776716 CCTGTCTCTACTAAAAAAAAGAAAAATTAGCCAGACGTGGTGGCATGCGCCTGTAATCCCAGCTA CCTGTCTCTACTAAAAAAAAGAAAAATTAGCCGGACGTGGTGGCATGCGCCTGTAATCCCAGCTA T C GNPNAT1 Ensembl:ENSG00000100522 Protein coding 3'UTR GSE38233;GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,32596459 RNA-Seq:(High) rs934468442 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124161,RMVar_hsa_circ_166733,RMVar_hsa_circ_113990,RMVar_hsa_circ_117524,RMVar_hsa_circ_166734,RMVar_hsa_circ_166735 41688 RMVar_ID_41688 Human_SNP_ID_555429767 A-to-I Human chr14 - 52785066 52785066 52785066 AAAAAATTAGCCGGGCGTGGTGTCACGTGCCTATAATCCCAGATACTCAGGAGGCTGAAAGAGGA AAAAAATTAGCCGGGCGTGGTGTCACGTGCCTGTAATCCCAGATACTCAGGAGGCTGAAAGAGGA T C GNPNAT1 Ensembl:ENSG00000100522 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1227503280 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8405182 RMVar_hsa_circ_297290 41689 RMVar_ID_41689 Human_SNP_ID_555450337 A-to-I Human chr14 - 52862582 52862582 52862582 CGCACTGCAGCCTCCATCTCCCAGGCTCAAGCAATCCTCCCACCTCAGCCTCCCTAGTAACTAGA CGCACTGCAGCCTCCATCTCCCAGGCTCAAGCCATCCTCCCACCTCAGCCTCCCTAGTAACTAGA T G FERMT2 Ensembl:ENSG00000073712 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1448563949 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29651,RMVar_hsa_circ_125561,RMVar_hsa_circ_32334,RMVar_hsa_circ_166738,RMVar_hsa_circ_166739,RMVar_hsa_circ_9284,RMVar_hsa_circ_166741,RMVar_hsa_circ_283795,RMVar_hsa_circ_311744,RMVar_hsa_circ_166740 41690 RMVar_ID_41690 Human_SNP_ID_555450339 A-to-I Human chr14 - 52862585 52862585 52862585 AAGCGCACTGCAGCCTCCATCTCCCAGGCTCAAGCAATCCTCCCACCTCAGCCTCCCTAGTAACT AAGCGCACTGCAGCCTCCATCTCCCAGGCTCAGGCAATCCTCCCACCTCAGCCTCCCTAGTAACT T C FERMT2 Ensembl:ENSG00000073712 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs975519985 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29651,RMVar_hsa_circ_125561,RMVar_hsa_circ_32334,RMVar_hsa_circ_166738,RMVar_hsa_circ_166739,RMVar_hsa_circ_9284,RMVar_hsa_circ_166741,RMVar_hsa_circ_283795,RMVar_hsa_circ_311744,RMVar_hsa_circ_166740 41691 RMVar_ID_41691 Human_SNP_ID_555451011 A-to-I Human chr14 - 52865156 52865156 52865156 CCACCACCCCCGGCTAATTTTTTGTATTTAGTAGAGACATGGTTTCACCATGTTGGTCAGCTGGT CCACCACCCCCGGCTAATTTTTTGTATTTAGTGGAGACATGGTTTCACCATGTTGGTCAGCTGGT T C FERMT2 Ensembl:ENSG00000073712 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1172245024 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25101792 RMVar_hsa_circ_125561,RMVar_hsa_circ_32334,RMVar_hsa_circ_166738,RMVar_hsa_circ_94152,RMVar_hsa_circ_9284,RMVar_hsa_circ_166741,RMVar_hsa_circ_311744,RMVar_hsa_circ_347037,RMVar_hsa_circ_166742 41692 RMVar_ID_41692 Human_SNP_ID_555469814 A-to-I Human chr14 - 52938707 52938707 52938707 CAAAAATTAGCTGGGTGTGGTGGTTCATGCCTATGGTCTCAGTTACTTGGGAGGCTGAGGCAGGA CAAAAATTAGCTGGGTGTGGTGGTTCATGCCTGTGGTCTCAGTTACTTGGGAGGCTGAGGCAGGA T C FERMT2 Ensembl:ENSG00000073712 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs539524334 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12267 41693 RMVar_ID_41693 Human_SNP_ID_555469962 A-to-I Human chr14 - 52939321 52939321 52939321 TCGCCCAGGCTGGAGTGCAGTGATGTGCTGTCAGCTCACTGCAACCTTCACCTCCCAGGTTCAAG TCGCCCAGGCTGGAGTGCAGTGATGTGCTGTCGGCTCACTGCAACCTTCACCTCCCAGGTTCAAG T C FERMT2 Ensembl:ENSG00000073712 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1000868480 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12267 41694 RMVar_ID_41694 Human_SNP_ID_555471959 A-to-I Human chr14 - 52947267 52947267 52947267 CACCGTGTTAACCGGGATGGTCTTGATCTCCTAACCTCGTCATCCGCCTGCCTTGGCCTCCCAAA CACCGTGTTAACCGGGATGGTCTTGATCTCCTGACCTCGTCATCCGCCTGCCTTGGCCTCCCAAA T C FERMT2 Ensembl:ENSG00000073712 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1463426647 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12267 41695 RMVar_ID_41695 Human_SNP_ID_555472032 A-to-I Human chr14 - 52947476 52947476 52947476 TTTATTTATTTATTTATTTTTTACTTTTTGAGACGGGAGTCTCACTCTGTCGCCCAGACTGGAGT TTTATTTATTTATTTATTTTTTACTTTTTGAGGCGGGAGTCTCACTCTGTCGCCCAGACTGGAGT T C FERMT2 Ensembl:ENSG00000073712 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs945818516 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6356889 RMVar_hsa_circ_12267 41696 RMVar_ID_41696 Human_SNP_ID_555496671 A-to-I Human chr14 - 53050077 53050077 53050077 GAGTCCTTTACTGTACCTCTGTTTTGTGGTTCATCACATTCTACCATATATTATAATTACTTATT GAGTCCTTTACTGTACCTCTGTTTTGTGGTTCGTCACATTCTACCATATATTATAATTACTTATT T C DDHD1 Ensembl:ENSG00000100523 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1322220401 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269123 41697 RMVar_ID_41697 Human_SNP_ID_555496681 A-to-I Human chr14 - 53050100 53050100 53050100 TCTTTCATTCCTTAGAACTGAGAGAGTCCTTTACTGTACCTCTGTTTTGTGGTTCATCACATTCT TCTTTCATTCCTTAGAACTGAGAGAGTCCTTTTCTGTACCTCTGTTTTGTGGTTCATCACATTCT T A DDHD1 Ensembl:ENSG00000100523 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1179422000 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269123 41698 RMVar_ID_41698 Human_SNP_ID_555496776 A-to-I Human chr14 - 53050513 53050513 53050513 TAGAATGTGACGAACCGCAAAACATAGGTACAATAAAGGACTCTCTCAGTTCTAGGGAATGAAAG TAGAATGTGACGAACCGCAAAACATAGGTACAGTAAAGGACTCTCTCAGTTCTAGGGAATGAAAG T C DDHD1 Ensembl:ENSG00000100523 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1416086741 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269123 41699 RMVar_ID_41699 Human_SNP_ID_555516037 A-to-I Human chr14 - 53126505 53126505 53126505 AAAATTAGCTGGGGATGGTGGCGCATGCCTGTAGTCCCAGCTACTTGGGAGCTGAAGTGGGAGGA AAAATTAGCTGGGGATGGTGGCGCATGCCTGTGGTCCCAGCTACTTGGGAGCTGAAGTGGGAGGA T C DDHD1 Ensembl:ENSG00000100523 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs953299168 Functional Loss SNV dbSNP153 33..33 33 - - - 41700 RMVar_ID_41700 Human_SNP_ID_555580009 A-to-I Human chr14 + 53380391 53380391 53380391 AGAATTAAAAACATATGAACATGAAAACTTGTATATGAATATTCACAGCAGCATTATTTATAATA AGAATTAAAAACATATGAACATGAAAACTTGTGTATGAATATTCACAGCAGCATTATTTATAATA A G AL365295.1 Ensembl:ENSG00000237356 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1013597480 Functional Loss SNV dbSNP153 33..33 33 - - - 41701 RMVar_ID_41701 Human_SNP_ID_555580010 A-to-I Human chr14 + 53380391 53380391 53380391 AGAATTAAAAACATATGAACATGAAAACTTGTATATGAATATTCACAGCAGCATTATTTATAATA AGAATTAAAAACATATGAACATGAAAACTTGTTTATGAATATTCACAGCAGCATTATTTATAATA A T AL365295.1 Ensembl:ENSG00000237356 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1013597480 Functional Loss SNV dbSNP153 33..33 33 - - - 41702 RMVar_ID_41702 Human_SNP_ID_555723137 A-to-I Human chr14 - 53991945 53991945 53991945 ATCACTGGGCTGTTGGCCTGGACCTTGCAGCCACAATGGATTCAAGTTCGAAATACAGCAACTTC ATCACTGGGCTGTTGGCCTGGACCTTGCAGCCGCAATGGATTCAAGTTCGAAATACAGCAACTTC T C ATP5F1CP1 Ensembl:ENSG00000224004 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1346696575 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5246768 41703 RMVar_ID_41703 Human_SNP_ID_555870029 A-to-I Human chr14 + 54590380 54590380 54590380 GGGCATGGTGGTGTGTGCCTGTAGCCGCAGCTACTTGAGAGGCTGAGGTGGGAGGATCGCCTGAG GGGCATGGTGGTGTGTGCCTGTAGCCGCAGCTCCTTGAGAGGCTGAGGTGGGAGGATCGCCTGAG A C SAMD4A Ensembl:ENSG00000020577 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1192182206 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_282713 41704 RMVar_ID_41704 Human_SNP_ID_555870037 A-to-I Human chr14 + 54590416 54590416 54590416 GAGAGGCTGAGGTGGGAGGATCGCCTGAGCCCAGGAGGTCGAGGCTGCAGTGAGCCAAGATTGTG GAGAGGCTGAGGTGGGAGGATCGCCTGAGCCCGGGAGGTCGAGGCTGCAGTGAGCCAAGATTGTG A G SAMD4A Ensembl:ENSG00000020577 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs368155533 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_282713 41705 RMVar_ID_41705 Human_SNP_ID_555874371 A-to-I Human chr14 + 54607895 54607895 54607895 AAAATTAGCCAGGCATGGTGGTGCAAACCTCTAATCCCCGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTAGCCAGGCATGGTGGTGCAAACCTCTGATCCCCGCTACTCGGGAGGCTGAGGCAGGAGA A G SAMD4A Ensembl:ENSG00000020577 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1299027038 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76963,RMVar_hsa_circ_282713,RMVar_hsa_circ_111906,RMVar_hsa_circ_166776,RMVar_hsa_circ_166777 41706 RMVar_ID_41706 Human_SNP_ID_555961598 A-to-I Human chr14 - 54959196 54959196 54959196 TTTGTTTTGTTGTTTTTTGTTTTTGTAGAGACAGGGTCTCCCTATGTTACCCATGCTAGTCTTAA TTTGTTTTGTTGTTTTTTGTTTTTGTAGAGACGGGGTCTCCCTATGTTACCCATGCTAGTCTTAA T C WDHD1 Ensembl:ENSG00000198554 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1316617457 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3452534 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 41707 RMVar_ID_41707 Human_SNP_ID_555961627 A-to-I Human chr14 - 54959315 54959315 54959315 TGGCTCACTGCAGCCTCAACCCCCCAGACCCAAGCGATCTTTCCACCTCAGCCTCCCAAGTAACT TGGCTCACTGCAGCCTCAACCCCCCAGACCCAGGCGATCTTTCCACCTCAGCCTCCCAAGTAACT T C WDHD1 Ensembl:ENSG00000198554 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1222521253 Functional Loss SNV dbSNP153 33..33 33 - - - 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 41708 RMVar_ID_41708 Human_SNP_ID_555961733 A-to-I Human chr14 - 54959652 54959652 54959652 GTGATCCTCCTGCCTCACCCTACTGAGTAGCTATGACTACAGTTGTGCATCACCATGCCTGGTTA GTGATCCTCCTGCCTCACCCTACTGAGTAGCTGTGACTACAGTTGTGCATCACCATGCCTGGTTA T C WDHD1 Ensembl:ENSG00000198554 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1361682937 Functional Loss SNV dbSNP153 33..33 33 - - - 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 41709 RMVar_ID_41709 Human_SNP_ID_555962344 A-to-I Human chr14 - 54961974 54961974 54961974 AAATTAGCTGAGGGTGGTGGTATGTGCCTGTAATCCCAGCTACTCGGGAGGCTGAAGCAGGAGAA AAATTAGCTGAGGGTGGTGGTATGTGCCTGTAGTCCCAGCTACTCGGGAGGCTGAAGCAGGAGAA T C WDHD1 Ensembl:ENSG00000198554 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1331314275 Functional Loss SNV dbSNP153 33..33 33 - - - 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 41710 RMVar_ID_41710 Human_SNP_ID_555967148 A-to-I Human chr14 - 54980081 54980081 54980081 GGCTTAAGGGATCTTCCCGCCTCGGCCTCCCAAAGTGTTGGGATTACAGGCATGAGCCACTGTGC GGCTTAAGGGATCTTCCCGCCTCGGCCTCCCAGAGTGTTGGGATTACAGGCATGAGCCACTGTGC T C WDHD1 Ensembl:ENSG00000198554 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1462704383 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_765,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_302275,RMVar_hsa_circ_166799,RMVar_hsa_circ_11903,RMVar_hsa_circ_166798,RMVar_hsa_circ_345532,RMVar_hsa_circ_267068,RMVar_hsa_circ_166800,RMVar_hsa_circ_50752,RMVar_hsa_circ_166801,RMVar_hsa_circ_40458,RMVar_hsa_circ_375027,RMVar_hsa_circ_117317,RMVar_hsa_circ_166804,RMVar_hsa_circ_166805,RMVar_hsa_circ_297483,RMVar_hsa_circ_315743,RMVar_hsa_circ_321746,RMVar_hsa_circ_362896,RMVar_hsa_circ_304763,RMVar_hsa_circ_166808,RMVar_hsa_circ_166807 41711 RMVar_ID_41711 Human_SNP_ID_555967958 A-to-I Human chr14 - 54982982 54982982 54982982 TGTTGTATTTTTAGTAGAGATGGGGTTTTGTCATGTTGGCTAGGCTGGTTTTGAACTCCTGGCAT TGTTGTATTTTTAGTAGAGATGGGGTTTTGTCGTGTTGGCTAGGCTGGTTTTGAACTCCTGGCAT T C WDHD1 Ensembl:ENSG00000198554 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913646306 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_765,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_166799,RMVar_hsa_circ_11903,RMVar_hsa_circ_166798,RMVar_hsa_circ_267068,RMVar_hsa_circ_166800,RMVar_hsa_circ_50752,RMVar_hsa_circ_40458,RMVar_hsa_circ_375027,RMVar_hsa_circ_166805,RMVar_hsa_circ_315743,RMVar_hsa_circ_321746,RMVar_hsa_circ_362896,RMVar_hsa_circ_304763,RMVar_hsa_circ_166808,RMVar_hsa_circ_166810,RMVar_hsa_circ_285211,RMVar_hsa_circ_309156,RMVar_hsa_circ_367329,RMVar_hsa_circ_340444,RMVar_hsa_circ_307070,RMVar_hsa_circ_18515 41712 RMVar_ID_41712 Human_SNP_ID_555969780 A-to-I Human chr14 - 54989939 54989939 54989939 GTTGCCTCTGCCGGGCGTGATGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCCAAGGTGGGT GTTGCCTCTGCCGGGCGTGATGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGT T C WDHD1 Ensembl:ENSG00000198554 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1235561595 Functional Loss SNV dbSNP153 33..33 33 - - - 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 41713 RMVar_ID_41713 Human_SNP_ID_555971750 A-to-I Human chr14 - 54997216 54997216 54997216 TTGTGTAGGCCTGTAAACCCAGGTACTCAGGAAGCTGAGGCAGGAAAATCACTTGAGCCTGGGAG TTGTGTAGGCCTGTAAACCCAGGTACTCAGGACGCTGAGGCAGGAAAATCACTTGAGCCTGGGAG T G WDHD1 Ensembl:ENSG00000198554 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1467982402 Functional Loss SNV dbSNP153 33..33 33 - - - 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_7817,RMVar_hsa_circ_67253,RMVar_hsa_circ_362896,RMVar_hsa_circ_304763,RMVar_hsa_circ_166810,RMVar_hsa_circ_309156,RMVar_hsa_circ_307070,RMVar_hsa_circ_277434,RMVar_hsa_circ_301397,RMVar_hsa_circ_166812,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_346724,RMVar_hsa_circ_166815,RMVar_hsa_circ_300776,RMVar_hsa_circ_166817,RMVar_hsa_circ_928 41714 RMVar_ID_41714 Human_SNP_ID_555981379 A-to-I Human chr14 + 55035000 55035000 55035000 CTTCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGTGCACGCCACCACACCCGGCTAATTTTT CTTCTGCCTCAGCCTCCCAAGTAGCTGGGACTGCAGGTGCACGCCACCACACCCGGCTAATTTTT A G SOCS4 Ensembl:ENSG00000180008 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1482527703 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81619,RMVar_hsa_circ_166825 41715 RMVar_ID_41715 Human_SNP_ID_555981390 A-to-I Human chr14 + 55035041 55035040 55035041 CGCCACCACACCCGGCTAATTTTTGTGTTTTTAGTAGAGAGGAGATTTTGCCATGTTGGCGAGGC CGCCACCACACCCGGCTAATTTTTGTGTTTTT_GTAGAGAGGAGATTTTGCCATGTTGGCGAGGC TA T SOCS4 Ensembl:ENSG00000180008 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1269264525 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_81619,RMVar_hsa_circ_166825 41716 RMVar_ID_41716 Human_SNP_ID_555981391 A-to-I Human chr14 + 55035041 55035041 55035041 CGCCACCACACCCGGCTAATTTTTGTGTTTTTAGTAGAGAGGAGATTTTGCCATGTTGGCGAGGC CGCCACCACACCCGGCTAATTTTTGTGTTTTTCGTAGAGAGGAGATTTTGCCATGTTGGCGAGGC A C SOCS4 Ensembl:ENSG00000180008 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1331673970 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81619,RMVar_hsa_circ_166825 41717 RMVar_ID_41717 Human_SNP_ID_555981396 A-to-I Human chr14 + 55035061 55035061 55035061 TTTTGTGTTTTTAGTAGAGAGGAGATTTTGCCATGTTGGCGAGGCTGGTCTCAAACTCCTGACCT TTTTGTGTTTTTAGTAGAGAGGAGATTTTGCCGTGTTGGCGAGGCTGGTCTCAAACTCCTGACCT A G SOCS4 Ensembl:ENSG00000180008 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs554976589 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81619,RMVar_hsa_circ_166825 41718 RMVar_ID_41718 Human_SNP_ID_555981824 A-to-I Human chr14 + 55036924 55036924 55036924 ATCACTTGAGCCCAGGAGTTCAAGACCAGCCTAGATAACATGGCAGGACCCCATCTCTACAAAAA ATCACTTGAGCCCAGGAGTTCAAGACCAGCCTGGATAACATGGCAGGACCCCATCTCTACAAAAA A G SOCS4 Ensembl:ENSG00000180008 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs570494686 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81619,RMVar_hsa_circ_166825 41719 RMVar_ID_41719 Human_SNP_ID_555986371 A-to-I Human chr14 + 55054285 55054285 55054285 TCAGCCTATCGAAGCGAAGTAGCTGGGATTACAGGTGCCTTCCACCACGCCCAGCTAATTTTCTG TCAGCCTATCGAAGCGAAGTAGCTGGGATTACCGGTGCCTTCCACCACGCCCAGCTAATTTTCTG A C MAPK1IP1L Ensembl:ENSG00000168175 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1410580738 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112430,RMVar_hsa_circ_166826 41720 RMVar_ID_41720 Human_SNP_ID_555986377 A-to-I Human chr14 + 55054319 55054319 55054319 GTGCCTTCCACCACGCCCAGCTAATTTTCTGTATTTTTAGTTGAGATAGGGTTTTACCATTGGCC GTGCCTTCCACCACGCCCAGCTAATTTTCTGTGTTTTTAGTTGAGATAGGGTTTTACCATTGGCC A G MAPK1IP1L Ensembl:ENSG00000168175 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569843050 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12357659,Human_RBP_ID_18652124 RMVar_hsa_circ_112430,RMVar_hsa_circ_166826 41721 RMVar_ID_41721 Human_SNP_ID_555986733 A-to-I Human chr14 + 55055809 55055809 55055809 AAAATTAGCCGGGCGTGGTGGCACGTGCCTATAATCCCAGCTACTTGAGAGGCTCAGGTAGGAGA AAAATTAGCCGGGCGTGGTGGCACGTGCCTATGATCCCAGCTACTTGAGAGGCTCAGGTAGGAGA A G MAPK1IP1L Ensembl:ENSG00000168175 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs887447726 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112430,RMVar_hsa_circ_166826 41722 RMVar_ID_41722 Human_SNP_ID_555986751 A-to-I Human chr14 + 55055879 55055879 55055879 TTAAACCTGGGAGGCGGAGGTTGCAGTGAGTCAAGATCACACTACTGCACTTTAGCCTGGGTGGC TTAAACCTGGGAGGCGGAGGTTGCAGTGAGTCGAGATCACACTACTGCACTTTAGCCTGGGTGGC A G MAPK1IP1L Ensembl:ENSG00000168175 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs550158085 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8405599,Human_RBP_ID_12357743 RMVar_hsa_circ_112430,RMVar_hsa_circ_166826 41723 RMVar_ID_41723 Human_SNP_ID_555986752 A-to-I Human chr14 + 55055887 55055887 55055887 GGGAGGCGGAGGTTGCAGTGAGTCAAGATCACACTACTGCACTTTAGCCTGGGTGGCAGAGCGAG GGGAGGCGGAGGTTGCAGTGAGTCAAGATCACGCTACTGCACTTTAGCCTGGGTGGCAGAGCGAG A G MAPK1IP1L Ensembl:ENSG00000168175 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1397977260 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8405599,Human_RBP_ID_9784439,Human_RBP_ID_12357743,Human_RBP_ID_25126848 RMVar_hsa_circ_112430,RMVar_hsa_circ_166826 41724 RMVar_ID_41724 Human_SNP_ID_555986918 A-to-I Human chr14 + 55056549 55056549 55056549 TTTTTTGTTTTTGAGACGGAGTTTGCACTGTCACCCAGGCTGGAGTGCAGTGGCTTGATCTCAGC TTTTTTGTTTTTGAGACGGAGTTTGCACTGTCGCCCAGGCTGGAGTGCAGTGGCTTGATCTCAGC A G MAPK1IP1L Ensembl:ENSG00000168175 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1249846062 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17562556 RMVar_hsa_circ_112430,RMVar_hsa_circ_166826 41725 RMVar_ID_41725 Human_SNP_ID_555986919 A-to-I Human chr14 + 55056549 55056549 55056549 TTTTTTGTTTTTGAGACGGAGTTTGCACTGTCACCCAGGCTGGAGTGCAGTGGCTTGATCTCAGC TTTTTTGTTTTTGAGACGGAGTTTGCACTGTCTCCCAGGCTGGAGTGCAGTGGCTTGATCTCAGC A T MAPK1IP1L Ensembl:ENSG00000168175 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1249846062 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17562556 RMVar_hsa_circ_112430,RMVar_hsa_circ_166826 41726 RMVar_ID_41726 Human_SNP_ID_555986929 A-to-I Human chr14 + 55056579 55056579 55056579 TCACCCAGGCTGGAGTGCAGTGGCTTGATCTCAGCTCACTGCAAGCTCCGCCTCCTGGGTTCGCG TCACCCAGGCTGGAGTGCAGTGGCTTGATCTCGGCTCACTGCAAGCTCCGCCTCCTGGGTTCGCG A G MAPK1IP1L Ensembl:ENSG00000168175 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs566568322 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17562556 RMVar_hsa_circ_112430,RMVar_hsa_circ_166826 41727 RMVar_ID_41727 Human_SNP_ID_555986987 A-to-I Human chr14 + 55056716 55056716 55056716 TATTTTTAGTAGAGACGGGGTTTCACCTTGTTAGCCAGGATGGTCTCAATCTCCTGACTTCGTGA TATTTTTAGTAGAGACGGGGTTTCACCTTGTTGGCCAGGATGGTCTCAATCTCCTGACTTCGTGA A G MAPK1IP1L Ensembl:ENSG00000168175 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1382652940 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112430,RMVar_hsa_circ_166826 41728 RMVar_ID_41728 Human_SNP_ID_555987219 A-to-I Human chr14 + 55057487 55057487 55057487 TCTAGTATTAAACATTTAAATGAGCTGGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGG TCTAGTATTAAACATTTAAATGAGCTGGGCGCCGTGGCTCACGCCTGTAATCCCAGCACTTTGGG A C MAPK1IP1L Ensembl:ENSG00000168175 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs926640031 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6359374 RMVar_hsa_circ_112430,RMVar_hsa_circ_166826 41729 RMVar_ID_41729 Human_SNP_ID_555987220 A-to-I Human chr14 + 55057487 55057487 55057487 TCTAGTATTAAACATTTAAATGAGCTGGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGG TCTAGTATTAAACATTTAAATGAGCTGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG A G MAPK1IP1L Ensembl:ENSG00000168175 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs926640031 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6359374 RMVar_hsa_circ_112430,RMVar_hsa_circ_166826 41730 RMVar_ID_41730 Human_SNP_ID_555987290 A-to-I Human chr14 + 55057705 55057705 55057705 TTAAACTGAGGAGGCGGAGGTTACAGTGAACCAAGATCGCGCCACTGCACTCCAGTCTGGCGACA TTAAACTGAGGAGGCGGAGGTTACAGTGAACCGAGATCGCGCCACTGCACTCCAGTCTGGCGACA A G MAPK1IP1L Ensembl:ENSG00000168175 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1393665397 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25126850 RMVar_hsa_circ_112430,RMVar_hsa_circ_166826 41731 RMVar_ID_41731 Human_SNP_ID_555987509 A-to-I Human chr14 + 55058581 55058581 55058581 AGCCGGGTGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGCGGATCACG AGCCGGGTGCGGTGGCTCATGCCTGTAATCCCCGCACTTTGGGAGGCTGAGGCGGGCGGATCACG A C MAPK1IP1L Ensembl:ENSG00000168175 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1032715358 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112430,RMVar_hsa_circ_166826 41732 RMVar_ID_41732 Human_SNP_ID_555987510 A-to-I Human chr14 + 55058581 55058581 55058581 AGCCGGGTGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGCGGATCACG AGCCGGGTGCGGTGGCTCATGCCTGTAATCCCGGCACTTTGGGAGGCTGAGGCGGGCGGATCACG A G MAPK1IP1L Ensembl:ENSG00000168175 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1032715358 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112430,RMVar_hsa_circ_166826 41733 RMVar_ID_41733 Human_SNP_ID_555987552 A-to-I Human chr14 + 55058709 55058709 55058709 AAAAAATTAGCCGGGCATGGCGGCGCTTGCCTATAATCCCAGTTACTCAGGAGGCTGAGGCAGGA AAAAAATTAGCCGGGCATGGCGGCGCTTGCCTGTAATCCCAGTTACTCAGGAGGCTGAGGCAGGA A G MAPK1IP1L Ensembl:ENSG00000168175 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs923798041 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112430,RMVar_hsa_circ_166826 41734 RMVar_ID_41734 Human_SNP_ID_555987553 A-to-I Human chr14 + 55058717 55058717 55058717 AGCCGGGCATGGCGGCGCTTGCCTATAATCCCAGTTACTCAGGAGGCTGAGGCAGGAGAATCTCT AGCCGGGCATGGCGGCGCTTGCCTATAATCCCGGTTACTCAGGAGGCTGAGGCAGGAGAATCTCT A G MAPK1IP1L Ensembl:ENSG00000168175 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1439281630 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112430,RMVar_hsa_circ_166826 41735 RMVar_ID_41735 Human_SNP_ID_555988063 A-to-I Human chr14 + 55060357 55060357 55060357 CCACACTGGGCTAATCGTTTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGA CCACACTGGGCTAATCGTTTTTTTGTATTTTTCGTAGAGACGGGGTTTCACCGTGTTAGCCAGGA A C MAPK1IP1L Ensembl:ENSG00000168175 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1264672920 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112430,RMVar_hsa_circ_166826 41736 RMVar_ID_41736 Human_SNP_ID_555988187 A-to-I Human chr14 + 55060879 55060879 55060879 AAATTTGGGAGTACACACAGTGGCTCATGGCTATAATCCCAATACTTTGGGAGGCTGAGGCAGGA AAATTTGGGAGTACACACAGTGGCTCATGGCTGTAATCCCAATACTTTGGGAGGCTGAGGCAGGA A G MAPK1IP1L Ensembl:ENSG00000168175 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1399596955 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112430,RMVar_hsa_circ_166826 41737 RMVar_ID_41737 Human_SNP_ID_555988189 A-to-I Human chr14 + 55060887 55060887 55060887 GAGTACACACAGTGGCTCATGGCTATAATCCCAATACTTTGGGAGGCTGAGGCAGGAGGGTCCTT GAGTACACACAGTGGCTCATGGCTATAATCCCTATACTTTGGGAGGCTGAGGCAGGAGGGTCCTT A T MAPK1IP1L Ensembl:ENSG00000168175 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1234868013 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6359419 RMVar_hsa_circ_112430,RMVar_hsa_circ_166826 41738 RMVar_ID_41738 Human_SNP_ID_555988228 A-to-I Human chr14 + 55061032 55061032 55061032 ATTTGCTGGGCATGATGGCACACACCTGTAGTACCGGCTATTAGGGAGACTGAGGCAAGAAGATG ATTTGCTGGGCATGATGGCACACACCTGTAGTGCCGGCTATTAGGGAGACTGAGGCAAGAAGATG A G MAPK1IP1L Ensembl:ENSG00000168175 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941892024 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6359423,Human_RBP_ID_12357952 RMVar_hsa_circ_112430,RMVar_hsa_circ_166826 41739 RMVar_ID_41739 Human_SNP_ID_555988238 A-to-I Human chr14 + 55061059 55061059 55061059 GTAGTACCGGCTATTAGGGAGACTGAGGCAAGAAGATGACTTGAGCCCAGGAGGTCAAGATTGCA GTAGTACCGGCTATTAGGGAGACTGAGGCAAGTAGATGACTTGAGCCCAGGAGGTCAAGATTGCA A T MAPK1IP1L Ensembl:ENSG00000168175 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285396489 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6359425,Human_RBP_ID_8405608,Human_RBP_ID_12357952 RMVar_hsa_circ_112430,RMVar_hsa_circ_166826 41740 RMVar_ID_41740 Human_SNP_ID_555988243 A-to-I Human chr14 + 55061075 55061075 55061075 GGGAGACTGAGGCAAGAAGATGACTTGAGCCCAGGAGGTCAAGATTGCAGTGAGCTGTGATCTCT GGGAGACTGAGGCAAGAAGATGACTTGAGCCCGGGAGGTCAAGATTGCAGTGAGCTGTGATCTCT A G MAPK1IP1L Ensembl:ENSG00000168175 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs746753101 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6359427,Human_RBP_ID_12357955 RMVar_hsa_circ_112430,RMVar_hsa_circ_166826 41741 RMVar_ID_41741 Human_SNP_ID_556006332 A-to-I Human chr14 + 55135779 55135779 55135779 TAGAGACAGGGTTTTGCCATATTGCCCAGGCTAGTCTTGAACTCTTGGGCTCAAGCGATTTGCCC TAGAGACAGGGTTTTGCCATATTGCCCAGGCTGGTCTTGAACTCTTGGGCTCAAGCGATTTGCCC A G LGALS3 Ensembl:ENSG00000131981 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1343045395 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8405645 RMVar_hsa_circ_4779 41742 RMVar_ID_41742 Human_SNP_ID_556016017 A-to-I Human chr14 - 55172085 55172085 55172085 GAGGCTTGCAGATCACCTGAGGTCAGGAGTTCAGGACTAGTAGCCTGGCCAACTTGGTGAAACCC GAGGCTTGCAGATCACCTGAGGTCAGGAGTTCGGGACTAGTAGCCTGGCCAACTTGGTGAAACCC T C DLGAP5 Ensembl:ENSG00000126787 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1219537507 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12358757 RMVar_hsa_circ_62580,RMVar_hsa_circ_6189,RMVar_hsa_circ_36398,RMVar_hsa_circ_51117 41743 RMVar_ID_41743 Human_SNP_ID_556016973 A-to-I Human chr14 - 55174829 55174829 55174829 AAAATTATCCGGGCGTGGTGGTGCACGCCTGTAGTCCCAGCTACTCATGAGGCTAAGGCAGGAGA AAAATTATCCGGGCGTGGTGGTGCACGCCTGTGGTCCCAGCTACTCATGAGGCTAAGGCAGGAGA T C DLGAP5 Ensembl:ENSG00000126787 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1407676938 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_62580,RMVar_hsa_circ_6189,RMVar_hsa_circ_36398,RMVar_hsa_circ_51117 41744 RMVar_ID_41744 Human_SNP_ID_556045879 A-to-I Human chr14 + 55284755 55284755 55284755 TTTCCATCTCATCCTCCTGAGTAGATGGGACTACAGGCATGTGCCACCACGTCCAGCTGATTTTT TTTCCATCTCATCCTCCTGAGTAGATGGGACTGCAGGCATGTGCCACCACGTCCAGCTGATTTTT A G FBXO34 Ensembl:ENSG00000178974 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1457384484 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127359,RMVar_hsa_circ_166831 41745 RMVar_ID_41745 Human_SNP_ID_556045897 A-to-I Human chr14 + 55284825 55284825 55284825 TTTTGTAGAGATAGGGTTTCACGCCTTTGCCCAGGCTGGTCTTGAATTCCTGGACTCAAGTGATC TTTTGTAGAGATAGGGTTTCACGCCTTTGCCCGGGCTGGTCTTGAATTCCTGGACTCAAGTGATC A G FBXO34 Ensembl:ENSG00000178974 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474999910 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6360070 RMVar_hsa_circ_127359,RMVar_hsa_circ_166831 41746 RMVar_ID_41746 Human_SNP_ID_556046080 A-to-I Human chr14 + 55285481 55285481 55285481 CCAGGTTGGAAACAGAGCAGGTCAAAACTCCCATGCTGATCAGTAGTGGGATCGTGCCTGTGAAT CCAGGTTGGAAACAGAGCAGGTCAAAACTCCCGTGCTGATCAGTAGTGGGATCGTGCCTGTGAAT A G FBXO34,AL158801.5 Ensembl:ENSG00000178974,Ensembl:ENSG00000278818 Protein coding,Other intron,exon GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs543649082 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127359,RMVar_hsa_circ_166831 41747 RMVar_ID_41747 Human_SNP_ID_556047426 A-to-I Human chr14 + 55290889 55290889 55290889 TTGCCCAGGCTGGAGTGCAGTGGCACTATCTCAGCTCACTGCAACTTCTGCCTCCGGAGTTCAAG TTGCCCAGGCTGGAGTGCAGTGGCACTATCTCCGCTCACTGCAACTTCTGCCTCCGGAGTTCAAG A C FBXO34 Ensembl:ENSG00000178974 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903653295 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127359,RMVar_hsa_circ_166831 41748 RMVar_ID_41748 Human_SNP_ID_556047491 A-to-I Human chr14 + 55291061 55291061 55291061 GTTGGCCATGCTCGTCTTGAACTCCTGACCTTAAGTGATCCTCCTGCCTTGGCCTCCCAAAGTGC GTTGGCCATGCTCGTCTTGAACTCCTGACCTTGAGTGATCCTCCTGCCTTGGCCTCCCAAAGTGC A G FBXO34 Ensembl:ENSG00000178974 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1176481566 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127359,RMVar_hsa_circ_166831 41749 RMVar_ID_41749 Human_SNP_ID_556048321 A-to-I Human chr14 + 55294405 55294405 55294405 GACCTCCCAAGTTCAAGTGATCCTCTGACTTCAACCTCCCAAGTAGCTGGGAGTACATACGCACA GACCTCCCAAGTTCAAGTGATCCTCTGACTTCGACCTCCCAAGTAGCTGGGAGTACATACGCACA A G FBXO34 Ensembl:ENSG00000178974 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs918352523 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127359,RMVar_hsa_circ_166831 41750 RMVar_ID_41750 Human_SNP_ID_556049656 A-to-I Human chr14 + 55299078 55299078 55299078 ACAGCAATTTCGAAACCTGTAGGGTTTGGAGAAAAGTCTGACGAGGATGAGCTCATGGCGGAATT ACAGCAATTTCGAAACCTGTAGGGTTTGGAGAGAAGTCTGACGAGGATGAGCTCATGGCGGAATT A G FBXO34,CHMP4BP1 Ensembl:ENSG00000178974,Ensembl:ENSG00000258469 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1001916876 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_38542,Human_RBP_ID_119477,Human_RBP_ID_5563917,Human_RBP_ID_12359807 Human_miRNA_ID_1883500 RMVar_hsa_circ_127359,RMVar_hsa_circ_166831 41751 RMVar_ID_41751 Human_SNP_ID_556054181 A-to-I Human chr14 + 55316325 55316325 55316325 AATTCCACTACAGGCTGGGTGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGT AATTCCACTACAGGCTGGGTGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGT A G FBXO34 Ensembl:ENSG00000178974 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1486172574 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127359,RMVar_hsa_circ_166831 41752 RMVar_ID_41752 Human_SNP_ID_556067669 A-to-I Human chr14 + 55364518 55364518 55364518 ACGATCTTGGATCACTGCAACCTCTGCCTCCTAGTTTCATGTGATTCTCCCGCCTCAGCCTCTTG ACGATCTTGGATCACTGCAACCTCTGCCTCCTGGTTTCATGTGATTCTCCCGCCTCAGCCTCTTG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1321011924 Functional Loss SNV dbSNP153 33..33 33 - - - 41753 RMVar_ID_41753 Human_SNP_ID_556068617 A-to-I Human chr14 - 55367526 55367526 55367526 GTTGGCCAGGCTGGTCTTGAACTCCTGACTTCAGGTGATCCGCTTGCCTTGGCCTCCTAAAGTGC GTTGGCCAGGCTGGTCTTGAACTCCTGACTTCCGGTGATCCGCTTGCCTTGGCCTCCTAAAGTGC T G ATG14 Ensembl:ENSG00000126775 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs111263526 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_166836,RMVar_hsa_circ_96031 41754 RMVar_ID_41754 Human_SNP_ID_556068629 A-to-I Human chr14 - 55367579 55367579 55367579 CCATCATGCCCAGCTAATTTTTGTATTTTAGTAAAGACGGGGGTTTTCACCATGTTGGCCAGGCT CCATCATGCCCAGCTAATTTTTGTATTTTAGTGAAGACGGGGGTTTTCACCATGTTGGCCAGGCT T C ATG14 Ensembl:ENSG00000126775 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1488153892 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_166836,RMVar_hsa_circ_96031 41755 RMVar_ID_41755 Human_SNP_ID_556068630 A-to-I Human chr14 - 55367582 55367582 55367582 CTGCCATCATGCCCAGCTAATTTTTGTATTTTAGTAAAGACGGGGGTTTTCACCATGTTGGCCAG CTGCCATCATGCCCAGCTAATTTTTGTATTTTCGTAAAGACGGGGGTTTTCACCATGTTGGCCAG T G ATG14 Ensembl:ENSG00000126775 Protein coding 3'UTR GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs994177479 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_166836,RMVar_hsa_circ_96031 41756 RMVar_ID_41756 Human_SNP_ID_556068641 A-to-I Human chr14 - 55367632 55367632 55367632 TCAAGCAATTCTTCCATCTCAACCTCCCGAGTAGCTGGGATTATAGGCACCTGCCATCATGCCCA TCAAGCAATTCTTCCATCTCAACCTCCCGAGTGGCTGGGATTATAGGCACCTGCCATCATGCCCA T C ATG14 Ensembl:ENSG00000126775 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1436449004 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_166836,RMVar_hsa_circ_96031 41757 RMVar_ID_41757 Human_SNP_ID_556068647 A-to-I Human chr14 - 55367643 55367643 55367643 ATCTCCTGGGTTCAAGCAATTCTTCCATCTCAACCTCCCGAGTAGCTGGGATTATAGGCACCTGC ATCTCCTGGGTTCAAGCAATTCTTCCATCTCAGCCTCCCGAGTAGCTGGGATTATAGGCACCTGC T C ATG14 Ensembl:ENSG00000126775 Protein coding 3'UTR GSE47997;GSE100210;GSE107867 K562 cells&HepG2 cells;HepG2 cell line;ASD brains,temporal_cortex - 23474544,29129909,30559470 RNA-Seq:(High) rs1165776599 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_166836,RMVar_hsa_circ_96031 41758 RMVar_ID_41758 Human_SNP_ID_556068664 A-to-I Human chr14 - 55367700 55367700 55367700 TCACTCAGCTGCCCAGGCTGGAGTGTAGTGGCACCATCTCCGCTCACTGCAACCACCATCTCCTG TCACTCAGCTGCCCAGGCTGGAGTGTAGTGGCTCCATCTCCGCTCACTGCAACCACCATCTCCTG T A ATG14 Ensembl:ENSG00000126775 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1442374598 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12360324 RMVar_hsa_circ_166836,RMVar_hsa_circ_96031 41759 RMVar_ID_41759 Human_SNP_ID_556068863 A-to-I Human chr14 + 55368284 55368284 55368284 CTCTTGTTGCCCAGGCTGGAGTGCAATGGCACAATCTCGGCTCACTGCAACCTCTGCCTCCCGGT CTCTTGTTGCCCAGGCTGGAGTGCAATGGCACCATCTCGGCTCACTGCAACCTCTGCCTCCCGGT A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs979326224 Functional Loss SNV dbSNP153 33..33 33 - - - 41760 RMVar_ID_41760 Human_SNP_ID_556071821 A-to-I Human chr14 - 55378907 55378906 55378908 GCTCAGGAGTTAGAGACCAGCCTGGGAAACATAGTGAGACCTTGTCGCTACTAAAAATAAAAAAA GCTCAGGAGTTAGAGACCAGCCTGGGAAACA__GTGAGACCTTGTCGCTACTAAAAATAAAAAAA CTA C ATG14 Ensembl:ENSG00000126775 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893949650 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_49128,RMVar_hsa_circ_166836,RMVar_hsa_circ_96031,RMVar_hsa_circ_166838,RMVar_hsa_circ_315712,RMVar_hsa_circ_274100 41761 RMVar_ID_41761 Human_SNP_ID_556072049 A-to-I Human chr14 - 55379784 55379784 55379784 CGGGAGCTGGAGGTTGCAGTGATGCTGAGATCACACCACTGCACTCCAGCCTGAGTGACGGAATG CGGGAGCTGGAGGTTGCAGTGATGCTGAGATCTCACCACTGCACTCCAGCCTGAGTGACGGAATG T A ATG14 Ensembl:ENSG00000126775 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913876811 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49128,RMVar_hsa_circ_166836,RMVar_hsa_circ_96031,RMVar_hsa_circ_166838,RMVar_hsa_circ_315712,RMVar_hsa_circ_274100 41762 RMVar_ID_41762 Human_SNP_ID_556075027 A-to-I Human chr14 - 55391348 55391348 55391348 CCGCAGCCTCCCGAGTAGCTGGGATTACAGGCATGCGCCACCACGCCCAGCTAATTTTTGTATTT CCGCAGCCTCCCGAGTAGCTGGGATTACAGGCGTGCGCCACCACGCCCAGCTAATTTTTGTATTT T C ATG14 Ensembl:ENSG00000126775 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs182250085 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_166836,RMVar_hsa_circ_96031 41763 RMVar_ID_41763 Human_SNP_ID_556075028 A-to-I Human chr14 - 55391348 55391348 55391348 CCGCAGCCTCCCGAGTAGCTGGGATTACAGGCATGCGCCACCACGCCCAGCTAATTTTTGTATTT CCGCAGCCTCCCGAGTAGCTGGGATTACAGGCCTGCGCCACCACGCCCAGCTAATTTTTGTATTT T G ATG14 Ensembl:ENSG00000126775 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs182250085 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_166836,RMVar_hsa_circ_96031 41764 RMVar_ID_41764 Human_SNP_ID_556107857 A-to-I Human chr14 - 55517655 55517655 55517655 TATTTTTGAGACAGGTTCTCACTCCGTTGCTCAGGCTGCTCTCGAACCTCTGGGCTCAAGTGATC TATTTTTGAGACAGGTTCTCACTCCGTTGCTCGGGCTGCTCTCGAACCTCTGGGCTCAAGTGATC T C KTN1-AS1 Ensembl:ENSG00000186615 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1429477824 Functional Loss SNV dbSNP153 33..33 33 - - - 41765 RMVar_ID_41765 Human_SNP_ID_556116467 A-to-I Human chr14 - 55554463 55554463 55554463 CGGAAGTTGCAGTGAGCTGAGATGGCGCCACTACATTCCAGCCTGGGTGACAGAGCAAGACCCTG CGGAAGTTGCAGTGAGCTGAGATGGCGCCACTGCATTCCAGCCTGGGTGACAGAGCAAGACCCTG T C KTN1-AS1 Ensembl:ENSG00000186615 lincRNA intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1219355338 Functional Loss SNV dbSNP153 33..33 33 - - - 41766 RMVar_ID_41766 Human_SNP_ID_556116808 A-to-I Human chr14 - 55555874 55555874 55555874 ACAGTCTCGCTCTGTCACCCAGGCTGGAGTGCAGTGGTGCAATCTTGGCTCACTGTAAGCTCCCC ACAGTCTCGCTCTGTCACCCAGGCTGGAGTGCCGTGGTGCAATCTTGGCTCACTGTAAGCTCCCC T G KTN1-AS1 Ensembl:ENSG00000186615 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042287090 Functional Loss SNV dbSNP153 33..33 33 - - - 41767 RMVar_ID_41767 Human_SNP_ID_556123742 A-to-I Human chr14 + 55583448 55583448 55583448 CCCTAAAAAAAGTTATGATTTAGTATTTTACGAATCGTCCTAGCTACTACAGGGAGATTAAGAAC CCCTAAAAAAAGTTATGATTTAGTATTTTACGGATCGTCCTAGCTACTACAGGGAGATTAAGAAC A G KTN1 Ensembl:ENSG00000126777 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1273079517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12360734 RMVar_hsa_circ_166839,RMVar_hsa_circ_105200 41768 RMVar_ID_41768 Human_SNP_ID_556124108 A-to-I Human chr14 + 55584739 55584739 55584739 ATAACCCTCAAACACAGTATTACATAGCTTCTATGAGGGTAGGCTTTTTGTCTGTTTTATTGATG ATAACCCTCAAACACAGTATTACATAGCTTCTGTGAGGGTAGGCTTTTTGTCTGTTTTATTGATG A G KTN1 Ensembl:ENSG00000126777 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031988245 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3453006,Human_RBP_ID_17562563 RMVar_hsa_circ_166839,RMVar_hsa_circ_105200 41769 RMVar_ID_41769 Human_SNP_ID_556124109 A-to-I Human chr14 + 55584739 55584739 55584739 ATAACCCTCAAACACAGTATTACATAGCTTCTATGAGGGTAGGCTTTTTGTCTGTTTTATTGATG ATAACCCTCAAACACAGTATTACATAGCTTCTTTGAGGGTAGGCTTTTTGTCTGTTTTATTGATG A T KTN1 Ensembl:ENSG00000126777 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031988245 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3453006,Human_RBP_ID_17562563 RMVar_hsa_circ_166839,RMVar_hsa_circ_105200 41770 RMVar_ID_41770 Human_SNP_ID_556143804 A-to-I Human chr14 + 55657649 55657649 55657649 AAAAATGTATTCGGCTGGGTGTGGTAGTTCACAGTAGTAATCCCAGCACTTTGGGAGGCTGAGAC AAAAATGTATTCGGCTGGGTGTGGTAGTTCACGGTAGTAATCCCAGCACTTTGGGAGGCTGAGAC A G KTN1 Ensembl:ENSG00000126777 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs998375832 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6360735,Human_RBP_ID_12361633 RMVar_hsa_circ_9339,RMVar_hsa_circ_53501,RMVar_hsa_circ_359358,RMVar_hsa_circ_72947,RMVar_hsa_circ_45494,RMVar_hsa_circ_166840,RMVar_hsa_circ_11463,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_16572,RMVar_hsa_circ_8884,RMVar_hsa_circ_73582,RMVar_hsa_circ_56816,RMVar_hsa_circ_60279,RMVar_hsa_circ_359535,RMVar_hsa_circ_361777,RMVar_hsa_circ_296696,RMVar_hsa_circ_57727,RMVar_hsa_circ_62590,RMVar_hsa_circ_283552,RMVar_hsa_circ_166853,RMVar_hsa_circ_296596,RMVar_hsa_circ_358625,RMVar_hsa_circ_36198,RMVar_hsa_circ_369013,RMVar_hsa_circ_314233,RMVar_hsa_circ_74649,RMVar_hsa_circ_166854,RMVar_hsa_circ_166855 41771 RMVar_ID_41771 Human_SNP_ID_556147510 A-to-I Human chr14 - 55671657 55671657 55671657 AAAATCAAAATGTAGATTAAAAATCATTTCCTACTGTTTCTGCAAGGACGGATTTGTATTTTTCA AAAATCAAAATGTAGATTAAAAATCATTTCCTTCTGTTTCTGCAAGGACGGATTTGTATTTTTCA T A - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1471250846 Functional Loss SNV dbSNP153 33..33 33 - - - 41772 RMVar_ID_41772 Human_SNP_ID_556301411 A-to-I Human chr14 + 56293434 56293433 56293434 CACTTAGTTCTGTGGTATTGAATTGACGACGTAACCTCTCTGTGCCTGGCTTCCACATCTCCCAA CACTTAGTTCTGTGGTATTGAATTGACGACGT_ACCTCTCTGTGCCTGGCTTCCACATCTCCCAA TA T PELI2 Ensembl:ENSG00000139946 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs528892153 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_166867 41773 RMVar_ID_41773 Human_SNP_ID_556381882 A-to-I Human chr14 + 56613826 56613826 56613826 TAATGCCTGTAATCCCAGCACTTTGGGAAGCCAAAGTGGGAGGATCGCTTGAGCCCAGGAGTTTG TAATGCCTGTAATCCCAGCACTTTGGGAAGCCGAAGTGGGAGGATCGCTTGAGCCCAGGAGTTTG A G TMEM260 Ensembl:ENSG00000070269 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1376338541 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61772,RMVar_hsa_circ_275408,RMVar_hsa_circ_30768,RMVar_hsa_circ_360479,RMVar_hsa_circ_47286,RMVar_hsa_circ_166870,RMVar_hsa_circ_367805,RMVar_hsa_circ_33674,RMVar_hsa_circ_358524,RMVar_hsa_circ_64038,RMVar_hsa_circ_166872,RMVar_hsa_circ_113118,RMVar_hsa_circ_375265,RMVar_hsa_circ_166871 41774 RMVar_ID_41774 Human_SNP_ID_556530605 A-to-I Human chr14 - 57211857 57211855 57211857 CCTGTCTCAGAACACTTTTTTTTTGGAGACAGAGTCTTGCCCCAGGCTGGAGTGCAGTGATGCCA CCTGTCTCAGAACACTTTTTTTTTGGAGACAG__TCTTGCCCCAGGCTGGAGTGCAGTGATGCCA ACT A EXOC5 Ensembl:ENSG00000070367 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1415155466 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_12363330 RMVar_hsa_circ_26177,RMVar_hsa_circ_311794,RMVar_hsa_circ_323514,RMVar_hsa_circ_334395,RMVar_hsa_circ_60884,RMVar_hsa_circ_269440,RMVar_hsa_circ_46011,RMVar_hsa_circ_166876 41775 RMVar_ID_41775 Human_SNP_ID_556530606 A-to-I Human chr14 - 57211857 57211857 57211857 CCTGTCTCAGAACACTTTTTTTTTGGAGACAGAGTCTTGCCCCAGGCTGGAGTGCAGTGATGCCA CCTGTCTCAGAACACTTTTTTTTTGGAGACAGGGTCTTGCCCCAGGCTGGAGTGCAGTGATGCCA T C EXOC5 Ensembl:ENSG00000070367 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs923056742 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12363330 RMVar_hsa_circ_26177,RMVar_hsa_circ_311794,RMVar_hsa_circ_323514,RMVar_hsa_circ_334395,RMVar_hsa_circ_60884,RMVar_hsa_circ_269440,RMVar_hsa_circ_46011,RMVar_hsa_circ_166876 41776 RMVar_ID_41776 Human_SNP_ID_556530910 A-to-I Human chr14 - 57213266 57213266 57213266 ACAGTCCTCCCACCTCAGCTTCTTGAGTAGCTAGGACCACAGCTGCACACCACCATACCCAGCCA ACAGTCCTCCCACCTCAGCTTCTTGAGTAGCTTGGACCACAGCTGCACACCACCATACCCAGCCA T A EXOC5 Ensembl:ENSG00000070367 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1023942300 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26177,RMVar_hsa_circ_311794,RMVar_hsa_circ_323514,RMVar_hsa_circ_334395,RMVar_hsa_circ_60884,RMVar_hsa_circ_269440,RMVar_hsa_circ_46011,RMVar_hsa_circ_166876 41777 RMVar_ID_41777 Human_SNP_ID_556530911 A-to-I Human chr14 - 57213266 57213266 57213266 ACAGTCCTCCCACCTCAGCTTCTTGAGTAGCTAGGACCACAGCTGCACACCACCATACCCAGCCA ACAGTCCTCCCACCTCAGCTTCTTGAGTAGCTGGGACCACAGCTGCACACCACCATACCCAGCCA T C EXOC5 Ensembl:ENSG00000070367 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1023942300 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26177,RMVar_hsa_circ_311794,RMVar_hsa_circ_323514,RMVar_hsa_circ_334395,RMVar_hsa_circ_60884,RMVar_hsa_circ_269440,RMVar_hsa_circ_46011,RMVar_hsa_circ_166876 41778 RMVar_ID_41778 Human_SNP_ID_556580679 A-to-I Human chr14 + 57414156 57414156 57414156 CACAATTAGGCCAGATGTGGTGGCTCACGCCTATTATCCCAGCGTTTTGGGAGGCTGAGATGGTA CACAATTAGGCCAGATGTGGTGGCTCACGCCTGTTATCCCAGCGTTTTGGGAGGCTGAGATGGTA A G NAA30 Ensembl:ENSG00000139977 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1212517195 Functional Loss SNV dbSNP153 33..33 33 - - - 41779 RMVar_ID_41779 Human_SNP_ID_556679111 A-to-I Human chr14 - 57792847 57792846 57792847 AATTCTTTAGTGGTGATTTCTGAGATTTCGGTACACCCATCACCAAGCAATGAACACGGCACCCA AATTCTTTAGTGGTGATTTCTGAGATTTCGGT_CACCCATCACCAAGCAATGAACACGGCACCCA GT G SLC35F4 Ensembl:ENSG00000151812 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1297903557 Functional Loss DEL dbSNP153 33..33 33 - - - 41780 RMVar_ID_41780 Human_SNP_ID_556785412 A-to-I Human chr14 + 58224207 58224207 58224207 ATTTTTTAGTAGAGACAGGTTTCCGCCATGTTAGCCAGGTTGGTCTCAAACTCCTGACCTCAGGT ATTTTTTAGTAGAGACAGGTTTCCGCCATGTTGGCCAGGTTGGTCTCAAACTCCTGACCTCAGGT A G ACTR10 Ensembl:ENSG00000131966 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1566629072 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39132,RMVar_hsa_circ_356760,RMVar_hsa_circ_367880,RMVar_hsa_circ_166917,RMVar_hsa_circ_166916,RMVar_hsa_circ_166919,RMVar_hsa_circ_362438,RMVar_hsa_circ_80994,RMVar_hsa_circ_312124,RMVar_hsa_circ_377128,RMVar_hsa_circ_166921,RMVar_hsa_circ_166922,RMVar_hsa_circ_166923,RMVar_hsa_circ_369470 41781 RMVar_ID_41781 Human_SNP_ID_556791775 A-to-I Human chr14 + 58248278 58248278 58248278 TGAGACCTGAGTCTCACTCTGTCACCTAGGCTAGAGTGCAGTGGCACGATCTTGGCTCACTGCAA TGAGACCTGAGTCTCACTCTGTCACCTAGGCTCGAGTGCAGTGGCACGATCTTGGCTCACTGCAA A C PSMA3 Ensembl:ENSG00000100567 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1258716768 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_166925,RMVar_hsa_circ_375117,RMVar_hsa_circ_343877 41782 RMVar_ID_41782 Human_SNP_ID_556791824 A-to-I Human chr14 + 58248450 58248450 58248450 CGGGGTTTTGCCACGTTGGCCAGGCTGGTCTCAAACCCCTGGCCTCAAGTGATCCGCTCACCTCG CGGGGTTTTGCCACGTTGGCCAGGCTGGTCTCGAACCCCTGGCCTCAAGTGATCCGCTCACCTCG A G PSMA3 Ensembl:ENSG00000100567 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs988616370 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_166925,RMVar_hsa_circ_375117,RMVar_hsa_circ_343877 41783 RMVar_ID_41783 Human_SNP_ID_556791925 A-to-I Human chr14 + 58248833 58248833 58248833 ACAAAATACAAAAATTAGCCGGGTGTGATGGCACACGTCGTAGTTTCAGCTACTTGGGAGGCTGA ACAAAATACAAAAATTAGCCGGGTGTGATGGCGCACGTCGTAGTTTCAGCTACTTGGGAGGCTGA A G PSMA3 Ensembl:ENSG00000100567 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs930186892 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_166925,RMVar_hsa_circ_375117,RMVar_hsa_circ_343877 41784 RMVar_ID_41784 Human_SNP_ID_556791940 A-to-I Human chr14 + 58248915 58248915 58248915 AACCTGGCAGGTGGACGTTGCAGTGAGCCAAGATTGCACCACTGCACTCCAGCCTAAGCAACAGA AACCTGGCAGGTGGACGTTGCAGTGAGCCAAGGTTGCACCACTGCACTCCAGCCTAAGCAACAGA A G PSMA3 Ensembl:ENSG00000100567 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs982447629 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17562564 RMVar_hsa_circ_166925,RMVar_hsa_circ_375117,RMVar_hsa_circ_343877 41785 RMVar_ID_41785 Human_SNP_ID_556792320 A-to-I Human chr14 + 58250244 58250243 58250245 TCCATCTCCAAAAAAAAAAAAAAAATAGGGACAGAGTTTCAAAATGTTGGCCTGGCTGGTCTTGA TCCATCTCCAAAAAAAAAAAAAAAATAGGGAC__AGTTTCAAAATGTTGGCCTGGCTGGTCTTGA CAG C PSMA3 Ensembl:ENSG00000100567 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1230485424 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_166925,RMVar_hsa_circ_375117,RMVar_hsa_circ_343877 41786 RMVar_ID_41786 Human_SNP_ID_556793749 A-to-I Human chr14 + 58255567 58255567 58255567 AAGGCGGGCGGATCACCTGAGGTCGAAAGTTCAAGACCAGCCTGACCAACATGGAGAAACCCTGT AAGGCGGGCGGATCACCTGAGGTCGAAAGTTCGAGACCAGCCTGACCAACATGGAGAAACCCTGT A G PSMA3 Ensembl:ENSG00000100567 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1250768275 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115365,RMVar_hsa_circ_166925,RMVar_hsa_circ_375117,RMVar_hsa_circ_343877,RMVar_hsa_circ_269887,RMVar_hsa_circ_166926,RMVar_hsa_circ_7202,RMVar_hsa_circ_17546,RMVar_hsa_circ_166927,RMVar_hsa_circ_166928,RMVar_hsa_circ_314483,RMVar_hsa_circ_368446 41787 RMVar_ID_41787 Human_SNP_ID_556794145 A-to-I Human chr14 + 58256861 58256861 58256861 CAAATTTGGGCCGGGCACGGCGGCTCACACCCATAATCCCAACATTTTGGGAGGCTGAGGCAGGC CAAATTTGGGCCGGGCACGGCGGCTCACACCCGTAATCCCAACATTTTGGGAGGCTGAGGCAGGC A G PSMA3 Ensembl:ENSG00000100567 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1267558474 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115365,RMVar_hsa_circ_166925,RMVar_hsa_circ_375117,RMVar_hsa_circ_343877,RMVar_hsa_circ_269887,RMVar_hsa_circ_166926,RMVar_hsa_circ_7202,RMVar_hsa_circ_17546,RMVar_hsa_circ_166927,RMVar_hsa_circ_166928,RMVar_hsa_circ_314483,RMVar_hsa_circ_368446 41788 RMVar_ID_41788 Human_SNP_ID_556794199 A-to-I Human chr14 + 58257077 58257077 58257077 TGAGCCCAGATGGTGCCATTGTGCTCCAGCCTAGGTGACACAGTGAGACTCTGTCTCAAAAAAAA TGAGCCCAGATGGTGCCATTGTGCTCCAGCCTGGGTGACACAGTGAGACTCTGTCTCAAAAAAAA A G PSMA3 Ensembl:ENSG00000100567 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs966185427 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115365,RMVar_hsa_circ_166925,RMVar_hsa_circ_375117,RMVar_hsa_circ_343877,RMVar_hsa_circ_269887,RMVar_hsa_circ_166926,RMVar_hsa_circ_7202,RMVar_hsa_circ_17546,RMVar_hsa_circ_166927,RMVar_hsa_circ_166928,RMVar_hsa_circ_314483,RMVar_hsa_circ_368446 41789 RMVar_ID_41789 Human_SNP_ID_556794599 A-to-I Human chr14 - 58258402 58258402 58258402 AGAGGCAGAGTCTCTATTGCGCCAGCTAGAGTACAGTGGTATGGCCACAGCTCATTCCAGCCTTC AGAGGCAGAGTCTCTATTGCGCCAGCTAGAGTGCAGTGGTATGGCCACAGCTCATTCCAGCCTTC T C ARMH4 Ensembl:ENSG00000139971 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs979388862 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6363204 41790 RMVar_ID_41790 Human_SNP_ID_556799258 A-to-I Human chr14 - 58274694 58274694 58274694 TTGTAGAGAAAAGGTCTCTCACTACGTTGCTTAGGCTGGTCTTGAACTCCTGGGTTCAAGCGATC TTGTAGAGAAAAGGTCTCTCACTACGTTGCTTGGGCTGGTCTTGAACTCCTGGGTTCAAGCGATC T C ARMH4,PSMA3-AS1 Ensembl:ENSG00000139971,Ensembl:ENSG00000257621 Protein coding,lincRNA intron,intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1412695575 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_166941,RMVar_hsa_circ_270215,RMVar_hsa_circ_351031,RMVar_hsa_circ_166942 41791 RMVar_ID_41791 Human_SNP_ID_556803405 A-to-I Human chr14 - 58289941 58289941 58289941 GAGGCCAGGAGTTTGAGACCAGCCTGGCCAACATTGTGAAACCTCATTTCTACTAAAACTACGAA GAGGCCAGGAGTTTGAGACCAGCCTGGCCAACGTTGTGAAACCTCATTTCTACTAAAACTACGAA T C ARMH4,PSMA3-AS1 Ensembl:ENSG00000139971,Ensembl:ENSG00000257621 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947727838 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_270215,RMVar_hsa_circ_166942,RMVar_hsa_circ_166943,RMVar_hsa_circ_288391,RMVar_hsa_circ_358954 41792 RMVar_ID_41792 Human_SNP_ID_556803641 A-to-I Human chr14 - 58290850 58290850 58290850 TAATTTTTGTGCTTTTAGTAGAGATGGGTTTCACCATATTGGCCCGGCTGCTCTCGAACTCCTGA TAATTTTTGTGCTTTTAGTAGAGATGGGTTTCGCCATATTGGCCCGGCTGCTCTCGAACTCCTGA T C ARMH4,PSMA3-AS1 Ensembl:ENSG00000139971,Ensembl:ENSG00000257621 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs986101576 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5246840 RMVar_hsa_circ_270215,RMVar_hsa_circ_166942,RMVar_hsa_circ_166944,RMVar_hsa_circ_166943,RMVar_hsa_circ_288391,RMVar_hsa_circ_358954 41793 RMVar_ID_41793 Human_SNP_ID_556803646 A-to-I Human chr14 - 58290863 58290863 58290863 CACCACGCCCGGCTAATTTTTGTGCTTTTAGTAGAGATGGGTTTCACCATATTGGCCCGGCTGCT CACCACGCCCGGCTAATTTTTGTGCTTTTAGTGGAGATGGGTTTCACCATATTGGCCCGGCTGCT T C ARMH4,PSMA3-AS1 Ensembl:ENSG00000139971,Ensembl:ENSG00000257621 Protein coding,lincRNA intron,intron GSE100210;GSE105773 HepG2 cell line;Glioblastoma cells,U87MG - 29129909,29724793 RNA-Seq:(High) rs930700221 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5246840 RMVar_hsa_circ_270215,RMVar_hsa_circ_166942,RMVar_hsa_circ_166944,RMVar_hsa_circ_166943,RMVar_hsa_circ_288391,RMVar_hsa_circ_358954 41794 RMVar_ID_41794 Human_SNP_ID_556803647 A-to-I Human chr14 - 58290866 58290866 58290866 TGCCACCACGCCCGGCTAATTTTTGTGCTTTTAGTAGAGATGGGTTTCACCATATTGGCCCGGCT TGCCACCACGCCCGGCTAATTTTTGTGCTTTTGGTAGAGATGGGTTTCACCATATTGGCCCGGCT T C ARMH4,PSMA3-AS1 Ensembl:ENSG00000139971,Ensembl:ENSG00000257621 Protein coding,lincRNA intron,intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1378808547 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_270215,RMVar_hsa_circ_166942,RMVar_hsa_circ_166944,RMVar_hsa_circ_166943,RMVar_hsa_circ_288391,RMVar_hsa_circ_358954 41795 RMVar_ID_41795 Human_SNP_ID_556803667 A-to-I Human chr14 - 58290907 58290907 58290907 TCCTGCCTCAGCCTCCTGGGTAGCTTGGGACTACAGGTGCATGCCACCACGCCCGGCTAATTTTT TCCTGCCTCAGCCTCCTGGGTAGCTTGGGACTGCAGGTGCATGCCACCACGCCCGGCTAATTTTT T C ARMH4,PSMA3-AS1 Ensembl:ENSG00000139971,Ensembl:ENSG00000257621 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs552660870 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_270215,RMVar_hsa_circ_166942,RMVar_hsa_circ_166944,RMVar_hsa_circ_166943,RMVar_hsa_circ_288391,RMVar_hsa_circ_358954 41796 RMVar_ID_41796 Human_SNP_ID_556803720 A-to-I Human chr14 - 58291076 58291076 58291076 TATTTGTAACCAAAGCAGACTTTGAAATTTCTATGTTGTCTTTTGCCCTATTCAATTTTTATTTA TATTTGTAACCAAAGCAGACTTTGAAATTTCTGTGTTGTCTTTTGCCCTATTCAATTTTTATTTA T C ARMH4,PSMA3-AS1 Ensembl:ENSG00000139971,Ensembl:ENSG00000257621 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973275482 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_270215,RMVar_hsa_circ_166942,RMVar_hsa_circ_166944,RMVar_hsa_circ_166943,RMVar_hsa_circ_288391,RMVar_hsa_circ_358954 41797 RMVar_ID_41797 Human_SNP_ID_556804628 A-to-I Human chr14 - 58293844 58293844 58293844 AAGAGGCTGAGGTGGGATGATCACCTGAGTCCAGGAGATCAAGGCTCCAGTGAACCATGATTGTG AAGAGGCTGAGGTGGGATGATCACCTGAGTCCGGGAGATCAAGGCTCCAGTGAACCATGATTGTG T C ARMH4,PSMA3-AS1 Ensembl:ENSG00000139971,Ensembl:ENSG00000257621 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs532237132 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1519051,Human_Splice_Rec_1519078 Human_miRNA_ID_2509458,Human_miRNA_ID_2542153,Human_miRNA_ID_2544022,Human_miRNA_ID_2545874,Human_miRNA_ID_2547726,Human_miRNA_ID_2549590,Human_miRNA_ID_2551459,Human_miRNA_ID_2556872,Human_miRNA_ID_2558755,Human_miRNA_ID_2589170,Human_miRNA_ID_3179798,Human_miRNA_ID_3181749,Human_miRNA_ID_3181862,Human_miRNA_ID_3181976,Human_miRNA_ID_3182088,Human_miRNA_ID_3182202,Human_miRNA_ID_3182315,Human_miRNA_ID_3182634,Human_miRNA_ID_3182745,Human_miRNA_ID_3184522 RMVar_hsa_circ_3020,RMVar_hsa_circ_104013,RMVar_hsa_circ_166946,RMVar_hsa_circ_166947 41798 RMVar_ID_41798 Human_SNP_ID_556804648 A-to-I Human chr14 - 58293922 58293922 58293922 CATGGTGAAACCTCATCTCTACAAACAGTGCAAGAAATCAGCCAGCGTGGTGGCGTGCACCTGTG CATGGTGAAACCTCATCTCTACAAACAGTGCAGGAAATCAGCCAGCGTGGTGGCGTGCACCTGTG T C ARMH4,PSMA3-AS1 Ensembl:ENSG00000139971,Ensembl:ENSG00000257621 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1038692820 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1519078 RMVar_hsa_circ_3020,RMVar_hsa_circ_104013,RMVar_hsa_circ_166946,RMVar_hsa_circ_166947 41799 RMVar_ID_41799 Human_SNP_ID_556804667 A-to-I Human chr14 - 58293984 58293984 58293984 TAATCCCAGCACTTTGGGAGACCGAGGTGAGCAGATGGCTTGAGCCCAGGAGTTTGGGACAACAT TAATCCCAGCACTTTGGGAGACCGAGGTGAGCTGATGGCTTGAGCCCAGGAGTTTGGGACAACAT T A ARMH4,PSMA3-AS1 Ensembl:ENSG00000139971,Ensembl:ENSG00000257621 Protein coding,lincRNA intron,intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs547295508 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1502620,Human_RBP_ID_25104211 RMVar_hsa_circ_3020,RMVar_hsa_circ_104013,RMVar_hsa_circ_166947 41800 RMVar_ID_41800 Human_SNP_ID_556805199 A-to-I Human chr14 - 58295740 58295740 58295740 CGGCTCACTACAACCTCTGCCTCCCAGGTTCAAGCAATTCTTCTGCCTCAGCCTCCCGAGTAGCT CGGCTCACTACAACCTCTGCCTCCCAGGTTCATGCAATTCTTCTGCCTCAGCCTCCCGAGTAGCT T A ARMH4,PSMA3-AS1 Ensembl:ENSG00000139971,Ensembl:ENSG00000257621 Protein coding,lincRNA intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1383419826 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1519050 RMVar_hsa_circ_3020,RMVar_hsa_circ_104013,RMVar_hsa_circ_166947 41801 RMVar_ID_41801 Human_SNP_ID_556832666 A-to-I Human chr14 - 58399152 58399152 58399152 GCCAGGCACAGTGGCTCCCTCGTGTAATCCCAACACTTCAGGAGGCCAAGGCCGGCAGACTGCTT GCCAGGCACAGTGGCTCCCTCGTGTAATCCCAGCACTTCAGGAGGCCAAGGCCGGCAGACTGCTT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1466436493 Functional Loss SNV dbSNP153 33..33 33 - - - 41802 RMVar_ID_41802 Human_SNP_ID_556834453 A-to-I Human chr14 - 58405785 58405783 58405785 AAGAACTATTAGGGGGGTGGGTGTGGTGGCTCACGCCTGTAATCCCAACACTTTGGGAGGCTGAG AAGAACTATTAGGGGGGTGGGTGTGGTGGCTC__GCCTGTAATCCCAACACTTTGGGAGGCTGAG CGT C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1295167851 Functional Loss DEL dbSNP153 33..34 33 - - - 41803 RMVar_ID_41803 Human_SNP_ID_556835899 A-to-I Human chr14 - 58411632 58411632 58411632 TGGGAGGCTGAGGCACAGGAATTGCTTGACCCAGGAAGCAGAGGCTGCAGTGAGCCGAGATCGTG TGGGAGGCTGAGGCACAGGAATTGCTTGACCCGGGAAGCAGAGGCTGCAGTGAGCCGAGATCGTG T C TIMM9 Ensembl:ENSG00000100575 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982748740 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_166961,RMVar_hsa_circ_300431,RMVar_hsa_circ_280391,RMVar_hsa_circ_166960 41804 RMVar_ID_41804 Human_SNP_ID_556838663 A-to-I Human chr14 - 58422892 58422892 58422892 AGGCACAAAATCACTTGAACCCAGGAGGCGGAAGATGTAGTAAGCTGAAATTGCACCACTGTACT AGGCACAAAATCACTTGAACCCAGGAGGCGGACGATGTAGTAAGCTGAAATTGCACCACTGTACT T G TIMM9 Ensembl:ENSG00000100575 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017270271 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12368337 RMVar_hsa_circ_166961,RMVar_hsa_circ_280391,RMVar_hsa_circ_61801 41805 RMVar_ID_41805 Human_SNP_ID_556838696 A-to-I Human chr14 - 58423017 58423017 58423017 GTGGATTACCTGAGGTCGGGAGTTCAAGACCAACCTGGCCAACATGGTGAAACCCCATCTATACT GTGGATTACCTGAGGTCGGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCCCATCTATACT T C TIMM9 Ensembl:ENSG00000100575 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1364299002 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_166961,RMVar_hsa_circ_280391,RMVar_hsa_circ_61801 41806 RMVar_ID_41806 Human_SNP_ID_556839336 A-to-I Human chr14 - 58425931 58425931 58425931 TTTTGTATTTTTATTAGAGACGGGGTTTCACCATGTTGGCCAGGTTGGTCTCGAACTCCTGACTT TTTTGTATTTTTATTAGAGACGGGGTTTCACCGTGTTGGCCAGGTTGGTCTCGAACTCCTGACTT T C TIMM9 Ensembl:ENSG00000100575 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1446053753 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37823 41807 RMVar_ID_41807 Human_SNP_ID_556839344 A-to-I Human chr14 - 58425957 58425957 58425957 GCCCGCCACCACGCCCAGCTAATTTTTTTTGTATTTTTATTAGAGACGGGGTTTCACCATGTTGG GCCCGCCACCACGCCCAGCTAATTTTTTTTGTGTTTTTATTAGAGACGGGGTTTCACCATGTTGG T C TIMM9 Ensembl:ENSG00000100575 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs938096246 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37823 41808 RMVar_ID_41808 Human_SNP_ID_556841301 A-to-I Human chr14 + 58433341 58433341 58433341 CGCCCACCTTGGTCTCCCACAGTGCTGGGATTACAGGTGTGAGCCACCATGATCAGCCTTCAGTT CGCCCACCTTGGTCTCCCACAGTGCTGGGATTGCAGGTGTGAGCCACCATGATCAGCCTTCAGTT A G KIAA0586 Ensembl:ENSG00000100578 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1430018529 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1519957 RMVar_hsa_circ_64129,RMVar_hsa_circ_310908,RMVar_hsa_circ_68375 41809 RMVar_ID_41809 Human_SNP_ID_556858768 A-to-I Human chr14 + 58502275 58502275 58502275 CTCCTACCTCAGCCTCCTGAGTAGCTGGGACTACAGATGCACGCCGCCACCTCGCCTGGCTGATT CTCCTACCTCAGCCTCCTGAGTAGCTGGGACTGCAGATGCACGCCGCCACCTCGCCTGGCTGATT A G KIAA0586 Ensembl:ENSG00000100578 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs948490719 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_68375,RMVar_hsa_circ_370405,RMVar_hsa_circ_166963,RMVar_hsa_circ_74600,RMVar_hsa_circ_300659,RMVar_hsa_circ_74383,RMVar_hsa_circ_31988,RMVar_hsa_circ_55729,RMVar_hsa_circ_24838,RMVar_hsa_circ_74381,RMVar_hsa_circ_125260,RMVar_hsa_circ_341833,RMVar_hsa_circ_344134,RMVar_hsa_circ_335034,RMVar_hsa_circ_166972,RMVar_hsa_circ_166971,RMVar_hsa_circ_274599,RMVar_hsa_circ_325294,RMVar_hsa_circ_334416,RMVar_hsa_circ_166975,RMVar_hsa_circ_166976,RMVar_hsa_circ_28384,RMVar_hsa_circ_277728,RMVar_hsa_circ_343426,RMVar_hsa_circ_291647,RMVar_hsa_circ_276618,RMVar_hsa_circ_166979,RMVar_hsa_circ_166980,RMVar_hsa_circ_166978 41810 RMVar_ID_41810 Human_SNP_ID_556870053 A-to-I Human chr14 + 58550019 58550019 58550019 GTCCATTCGACGGTTTCTTTTTTTTTTTTTTGAGATGGAATTTTGCTCGTTGCCCAGGCTGGAGT GTCCATTCGACGGTTTCTTTTTTTTTTTTTTGTGATGGAATTTTGCTCGTTGCCCAGGCTGGAGT A T KIAA0586 Ensembl:ENSG00000100578 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1200614859 Functional Loss SNV dbSNP153 33..33 33 - - - 41811 RMVar_ID_41811 Human_SNP_ID_556870080 A-to-I Human chr14 + 58550128 58550128 58550128 TCAAGCGATTCTCCTGCCTTAGCCTCCTTAGTAGCTGGGATTACAGGCGTGCGCCACCATGCCCG TCAAGCGATTCTCCTGCCTTAGCCTCCTTAGTTGCTGGGATTACAGGCGTGCGCCACCATGCCCG A T KIAA0586 Ensembl:ENSG00000100578 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs957606550 Functional Loss SNV dbSNP153 33..33 33 - - - 41812 RMVar_ID_41812 Human_SNP_ID_556870199 A-to-I Human chr14 + 58550573 58550573 58550573 TATTGCTGGGCTGTGACTGGACACGGTGGCTCATGCCTGTAATCCCAAGACTTTGGGAGGCCGAG TATTGCTGGGCTGTGACTGGACACGGTGGCTCGTGCCTGTAATCCCAAGACTTTGGGAGGCCGAG A G KIAA0586 Ensembl:ENSG00000100578 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1226188982 Functional Loss SNV dbSNP153 33..33 33 - - - 41813 RMVar_ID_41813 Human_SNP_ID_556870240 A-to-I Human chr14 + 58550727 58550727 58550727 ATGGTTGCACACACCTGTAGCCCCAGCTACTCAAGAGGGTGAGGTGAGAGGATCGCTTGAGCCCA ATGGTTGCACACACCTGTAGCCCCAGCTACTCGAGAGGGTGAGGTGAGAGGATCGCTTGAGCCCA A G KIAA0586 Ensembl:ENSG00000100578 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170941183 Functional Loss SNV dbSNP153 33..33 33 - - - 41814 RMVar_ID_41814 Human_SNP_ID_557010831 A-to-I Human chr14 - 59136178 59136177 59136179 GAGCTCTTCATCATCAGCAAACTCTGGTGCACATACCATGGGAAGGGCCTGGTGAAAGGAGCCTG GAGCTCTTCATCATCAGCAAACTCTGGTGCA__TACCATGGGAAGGGCCTGGTGAAAGGAGCCTG ATG A AL359219.1 Ensembl:ENSG00000258685 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1566626595 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_5564109 41815 RMVar_ID_41815 Human_SNP_ID_557010832 A-to-I Human chr14 - 59136178 59136178 59136178 GAGCTCTTCATCATCAGCAAACTCTGGTGCACATACCATGGGAAGGGCCTGGTGAAAGGAGCCTG GAGCTCTTCATCATCAGCAAACTCTGGTGCACCTACCATGGGAAGGGCCTGGTGAAAGGAGCCTG T G AL359219.1 Ensembl:ENSG00000258685 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs959492628 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5564109 41816 RMVar_ID_41816 Human_SNP_ID_557010834 A-to-I Human chr14 - 59136190 59136190 59136190 GTGAAGCGTGAGGAGCTCTTCATCATCAGCAAACTCTGGTGCACATACCATGGGAAGGGCCTGGT GTGAAGCGTGAGGAGCTCTTCATCATCAGCAATCTCTGGTGCACATACCATGGGAAGGGCCTGGT T A AL359219.1 Ensembl:ENSG00000258685 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1163999196 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5564109 41817 RMVar_ID_41817 Human_SNP_ID_557113922 A-to-I Human chr14 - 59547022 59547022 59547022 TTGCCCAGGCTGGTCTCTAACTCCTGGGCTCAAGTGATCCTCCCACCTCCGCCTCTCAAAGTGCT TTGCCCAGGCTGGTCTCTAACTCCTGGGCTCAGGTGATCCTCCCACCTCCGCCTCTCAAAGTGCT T C CCDC175 Ensembl:ENSG00000151838 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs534259675 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2006,RMVar_hsa_circ_166999,RMVar_hsa_circ_167003,RMVar_hsa_circ_265313,RMVar_hsa_circ_3540,RMVar_hsa_circ_17329,RMVar_hsa_circ_167008,RMVar_hsa_circ_298010 41818 RMVar_ID_41818 Human_SNP_ID_557133107 A-to-I Human chr14 - 59628213 59628213 59628213 ATTTTTTGAAAAGCTCCCTAGGTGAGTTTAATATGTAACCAGGGTTGAAGTCACTGGAATATTAT ATTTTTTGAAAAGCTCCCTAGGTGAGTTTAATGTGTAACCAGGGTTGAAGTCACTGGAATATTAT T C RTN1 Ensembl:ENSG00000139970 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1020346379 Functional Loss SNV dbSNP153 33..33 33 - - - 41819 RMVar_ID_41819 Human_SNP_ID_216481871 A-to-I Human chr4 + 182300096 182300096 182300096 CACAGCCACGCCTGGCTAATTTCTGTATTTTTAGTAGAGACGAGGTTTCACCATGTTGGCAAGGC CACAGCCACGCCTGGCTAATTTCTGTATTTTTGGTAGAGACGAGGTTTCACCATGTTGGCAAGGC A G TENM3 Ensembl:ENSG00000218336 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985714271 Functional Loss SNV dbSNP153 33..33 33 - - - 41820 RMVar_ID_41820 Human_SNP_ID_216521559 A-to-I Human chr4 + 182462230 182462230 182462230 GGCCCACACATTGCCACACCTGGCCAATTTTTAAATTTTCAGTAAAGACTGAGTCTCGCTACGTT GGCCCACACATTGCCACACCTGGCCAATTTTTCAATTTTCAGTAAAGACTGAGTCTCGCTACGTT A C TENM3 Ensembl:ENSG00000218336 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs916220334 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 41821 RMVar_ID_41821 Human_SNP_ID_216573689 A-to-I Human chr4 + 182675485 182675481 182675485 ATTGCTTGAACCCTGGAGGCAAAGATTGCAGTAAGTGAGAGATCGTGACATTGCACTCCAGCCTG ATTGCTTGAACCCTGGAGGCAAAGATTGC____AGTGAGAGATCGTGACATTGCACTCCAGCCTG CAGTA C TENM3 Ensembl:ENSG00000218336 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1160264707 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_20593,RMVar_hsa_circ_96182,RMVar_hsa_circ_229674,RMVar_hsa_circ_319538,RMVar_hsa_circ_323028,RMVar_hsa_circ_340914,RMVar_hsa_circ_323573,RMVar_hsa_circ_320740,RMVar_hsa_circ_104629,RMVar_hsa_circ_229681,RMVar_hsa_circ_229684,RMVar_hsa_circ_229683,RMVar_hsa_circ_313387,RMVar_hsa_circ_370603 41822 RMVar_ID_41822 Human_SNP_ID_216573692 A-to-I Human chr4 + 182675485 182675485 182675485 ATTGCTTGAACCCTGGAGGCAAAGATTGCAGTAAGTGAGAGATCGTGACATTGCACTCCAGCCTG ATTGCTTGAACCCTGGAGGCAAAGATTGCAGTGAGTGAGAGATCGTGACATTGCACTCCAGCCTG A G TENM3 Ensembl:ENSG00000218336 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1275456202 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20593,RMVar_hsa_circ_96182,RMVar_hsa_circ_229674,RMVar_hsa_circ_319538,RMVar_hsa_circ_323028,RMVar_hsa_circ_340914,RMVar_hsa_circ_323573,RMVar_hsa_circ_320740,RMVar_hsa_circ_104629,RMVar_hsa_circ_229681,RMVar_hsa_circ_229684,RMVar_hsa_circ_229683,RMVar_hsa_circ_313387,RMVar_hsa_circ_370603 41823 RMVar_ID_41823 Human_SNP_ID_216783654 A-to-I Human chr4 + 183483824 183483824 183483824 CACACCAGGAGGGCGAGGAGACATGAAATATGACATATATGCTGTAGAGAATGAGCATATGAATC CACACCAGGAGGGCGAGGAGACATGAAATATGGCATATATGCTGTAGAGAATGAGCATATGAATC A G VTI1BP2 Ensembl:ENSG00000213434 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1358003806 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17409731 41824 RMVar_ID_41824 Human_SNP_ID_216783717 A-to-I Human chr4 + 183484062 183484062 183484062 ATAAACACAACTGAAAACTTGAGCAAAAGTCGAAAGATTCTCCGTTCAATGTCCAGAAAAGTGAC ATAAACACAACTGAAAACTTGAGCAAAAGTCGGAAGATTCTCCGTTCAATGTCCAGAAAAGTGAC A G VTI1BP2 Ensembl:ENSG00000213434 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879089586 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17409732 41825 RMVar_ID_41825 Human_SNP_ID_216826256 A-to-I Human chr4 - 183645043 183645043 183645043 CAAGCTGGAGTGCAGTGGCGTGAACATGGCTCACTGTAGCCTTGACCTCCCCAGATTAAGCGATC CAAGCTGGAGTGCAGTGGCGTGAACATGGCTCGCTGTAGCCTTGACCTCCCCAGATTAAGCGATC T C RWDD4 Ensembl:ENSG00000182552 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1289438293 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15109189 41826 RMVar_ID_41826 Human_SNP_ID_216843998 A-to-I Human chr4 + 183711656 183711656 183711656 GTTTCTGTATGTATGTACACACACACTGCTATATACATCTGAACAACCACAGCAGCAGCAAACTG GTTTCTGTATGTATGTACACACACACTGCTATGTACATCTGAACAACCACAGCAGCAGCAAACTG A G TRAPPC11 Ensembl:ENSG00000168538 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1261749998 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24047927 41827 RMVar_ID_41827 Human_SNP_ID_216868344 A-to-I Human chr4 + 183802797 183802797 183802797 GCGCCTGCCAACACACCTGGCTGATTTTTTGTATTTTTAGTAGAGACGGGGTCTCACCGTATTAG GCGCCTGCCAACACACCTGGCTGATTTTTTGTGTTTTTAGTAGAGACGGGGTCTCACCGTATTAG A G STOX2 Ensembl:ENSG00000173320 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1233818171 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15109399 41828 RMVar_ID_41828 Human_SNP_ID_216902088 A-to-I Human chr4 + 183939959 183939959 183939959 GGAATCTCGCTCTGTCGCTCAGGCTGGAGTGCAATGGCACGATCTCAGCTCACTGCAGCCTCCGC GGAATCTCGCTCTGTCGCTCAGGCTGGAGTGCGATGGCACGATCTCAGCTCACTGCAGCCTCCGC A G STOX2 Ensembl:ENSG00000173320 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1480404039 Functional Loss SNV dbSNP153 33..33 33 - - - 41829 RMVar_ID_41829 Human_SNP_ID_216905304 A-to-I Human chr4 + 183951868 183951868 183951868 AGGAGGCTGAGGCAGGAGAATCTCTTGAACCCAGGAGACAGAAGGTTGCAGTGAGCCGAGATAGC AGGAGGCTGAGGCAGGAGAATCTCTTGAACCCGGGAGACAGAAGGTTGCAGTGAGCCGAGATAGC A G STOX2 Ensembl:ENSG00000173320 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167757069 Functional Loss SNV dbSNP153 33..33 33 - - - 41830 RMVar_ID_41830 Human_SNP_ID_216921003 A-to-I Human chr4 + 184016267 184016267 184016267 TCTGTGGTCCCAGCTACTCGGGAGACTGAGGTAGGAGGATTGCTTCAGCCTGGGAGGCAGAGGTT TCTGTGGTCCCAGCTACTCGGGAGACTGAGGTGGGAGGATTGCTTCAGCCTGGGAGGCAGAGGTT A G STOX2,AC074194.2 Ensembl:ENSG00000173320,Ensembl:ENSG00000283355 Protein coding,Other intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs948166876 Functional Loss SNV dbSNP153 33..33 33 - - - 41831 RMVar_ID_41831 Human_SNP_ID_216992616 A-to-I Human chr4 - 184300019 184300019 184300019 TGGTCCCAGCACTTTGGGAGGCCGAGGTGGGCAGATCACCTGAGGTTGGGAGTTCGGGACGAGGC TGGTCCCAGCACTTTGGGAGGCCGAGGTGGGCGGATCACCTGAGGTTGGGAGTTCGGGACGAGGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1284366236 Functional Loss SNV dbSNP153 33..33 33 - - - 41832 RMVar_ID_41832 Human_SNP_ID_216992617 A-to-I Human chr4 - 184300019 184300019 184300019 TGGTCCCAGCACTTTGGGAGGCCGAGGTGGGCAGATCACCTGAGGTTGGGAGTTCGGGACGAGGC TGGTCCCAGCACTTTGGGAGGCCGAGGTGGGCCGATCACCTGAGGTTGGGAGTTCGGGACGAGGC T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1284366236 Functional Loss SNV dbSNP153 33..33 33 - - - 41833 RMVar_ID_41833 Human_SNP_ID_216992691 A-to-I Human chr4 - 184300316 184300316 184300316 GGTTTGGGTGGTTCTCCTACCTCGGCCTCCCAAGTGGCTGGGATTGCAGGCACATGCCACCATGC GGTTTGGGTGGTTCTCCTACCTCGGCCTCCCAGGTGGCTGGGATTGCAGGCACATGCCACCATGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1344695347 Functional Loss SNV dbSNP153 33..33 33 - - - 41834 RMVar_ID_41834 Human_SNP_ID_217003000 A-to-I Human chr4 - 184339293 184339293 184339293 GGCTCACTGAAACCTCCGCTTCCCAGGTTCAAACGATTCTCCTGCCTCAGCCTTCCGAGTAGCTG GGCTCACTGAAACCTCCGCTTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTTCCGAGTAGCTG T C LINC02363 Ensembl:ENSG00000180712 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs775262506 Functional Loss SNV dbSNP153 33..33 33 - - - 41835 RMVar_ID_41835 Human_SNP_ID_217003003 A-to-I Human chr4 - 184339301 184339301 184339301 GCGATCTTGGCTCACTGAAACCTCCGCTTCCCAGGTTCAAACGATTCTCCTGCCTCAGCCTTCCG GCGATCTTGGCTCACTGAAACCTCCGCTTCCCGGGTTCAAACGATTCTCCTGCCTCAGCCTTCCG T C LINC02363 Ensembl:ENSG00000180712 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs917442658 Functional Loss SNV dbSNP153 33..33 33 - - - 41836 RMVar_ID_41836 Human_SNP_ID_217003018 A-to-I Human chr4 - 184339338 184339338 184339338 GAGTCTCACTGTGACACCTAGTTTGGACTGCAATGGCGCGATCTTGGCTCACTGAAACCTCCGCT GAGTCTCACTGTGACACCTAGTTTGGACTGCAGTGGCGCGATCTTGGCTCACTGAAACCTCCGCT T C LINC02363 Ensembl:ENSG00000180712 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1418854579 Functional Loss SNV dbSNP153 33..33 33 - - - 41837 RMVar_ID_41837 Human_SNP_ID_217003240 A-to-I Human chr4 - 184340159 184340159 184340159 ATAATACTAAAAATACAAAAAATTAGCCGGGCATGGTGGTGGATGCCTGTAGTCCCAGGTACTCA ATAATACTAAAAATACAAAAAATTAGCCGGGCGTGGTGGTGGATGCCTGTAGTCCCAGGTACTCA T C LINC02363 Ensembl:ENSG00000180712 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs967437502 Functional Loss SNV dbSNP153 33..33 33 - - - 41838 RMVar_ID_41838 Human_SNP_ID_217003276 A-to-I Human chr4 - 184340267 184340267 184340267 AATGGGGCCGGGCACAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCAGA AATGGGGCCGGGCACAGTGGCTCACACCTGTAGTCCCAGCACTTTGGGAGGCCGAGGCGGGCAGA T C LINC02363 Ensembl:ENSG00000180712 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs971743194 Functional Loss SNV dbSNP153 33..33 33 - - - 41839 RMVar_ID_41839 Human_SNP_ID_217003412 A-to-I Human chr4 - 184340801 184340801 184340801 CTGGGAGACAGAGGTTGCAGTGGGCTGAGATCACGCCACTGCACTCCAGCATGGACAACAGAGCG CTGGGAGACAGAGGTTGCAGTGGGCTGAGATCGCGCCACTGCACTCCAGCATGGACAACAGAGCG T C LINC02363 Ensembl:ENSG00000180712 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs566938391 Functional Loss SNV dbSNP153 33..33 33 - - - 41840 RMVar_ID_41840 Human_SNP_ID_217003436 A-to-I Human chr4 - 184340876 184340876 184340876 AAATTAGCCAGGCATGGTAATGGGCATCTGTAATCCCAGCTACTCGCGAGGCTGAGGCAGGAGAA AAATTAGCCAGGCATGGTAATGGGCATCTGTAGTCCCAGCTACTCGCGAGGCTGAGGCAGGAGAA T C LINC02363 Ensembl:ENSG00000180712 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1317618776 Functional Loss SNV dbSNP153 33..33 33 - - - 41841 RMVar_ID_41841 Human_SNP_ID_217003439 A-to-I Human chr4 - 184340890 184340890 184340890 TACTAAACATACAAAAATTAGCCAGGCATGGTAATGGGCATCTGTAATCCCAGCTACTCGCGAGG TACTAAACATACAAAAATTAGCCAGGCATGGTGATGGGCATCTGTAATCCCAGCTACTCGCGAGG T C LINC02363 Ensembl:ENSG00000180712 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1224835052 Functional Loss SNV dbSNP153 33..33 33 - - - 41842 RMVar_ID_41842 Human_SNP_ID_217086796 A-to-I Human chr4 + 184678669 184678669 184678669 CCTGCCTCAGTCTCCCAAGTAGCTGGGACTACAGGCGCCTGCCACCACACCCGGCTAATTTTTGT CCTGCCTCAGTCTCCCAAGTAGCTGGGACTACGGGCGCCTGCCACCACACCCGGCTAATTTTTGT A G PRIMPOL Ensembl:ENSG00000164306 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1385594280 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268212,RMVar_hsa_circ_353567,RMVar_hsa_circ_229774,RMVar_hsa_circ_308765,RMVar_hsa_circ_229778,RMVar_hsa_circ_50557,RMVar_hsa_circ_303502,RMVar_hsa_circ_273995,RMVar_hsa_circ_229779,RMVar_hsa_circ_353862,RMVar_hsa_circ_271705,RMVar_hsa_circ_229786,RMVar_hsa_circ_229787,RMVar_hsa_circ_229785,RMVar_hsa_circ_336818,RMVar_hsa_circ_284575,RMVar_hsa_circ_271471,RMVar_hsa_circ_229789,RMVar_hsa_circ_28649,RMVar_hsa_circ_295530,RMVar_hsa_circ_369996,RMVar_hsa_circ_229790,RMVar_hsa_circ_362621,RMVar_hsa_circ_229791 41843 RMVar_ID_41843 Human_SNP_ID_217092051 A-to-I Human chr4 - 184698513 184698513 184698513 CTGGGAGGCGGAGGTTGCAGTGAGCTGAGATCACGCCACTGCACTCCCAGCCTGGGTGACAGAGC CTGGGAGGCGGAGGTTGCAGTGAGCTGAGATCGCGCCACTGCACTCCCAGCCTGGGTGACAGAGC T C CENPU Ensembl:ENSG00000151725 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs563821351 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25832559 RMVar_hsa_circ_17811 41844 RMVar_ID_41844 Human_SNP_ID_217092070 A-to-I Human chr4 - 184698588 184698588 184698588 AAACTTAGCCGGGCGTGGTGTGGGCACCTGTAATCCCAGCTACTCGAGAGGCTGAGGCAGGAGAA AAACTTAGCCGGGCGTGGTGTGGGCACCTGTAGTCCCAGCTACTCGAGAGGCTGAGGCAGGAGAA T C CENPU Ensembl:ENSG00000151725 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1320904703 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17811 41845 RMVar_ID_41845 Human_SNP_ID_217092200 A-to-I Human chr4 - 184699154 184699154 184699154 GGCTAATTTTTTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTAGTCAGGATGCTCTGGA GGCTAATTTTTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTAGTCAGGATGCTCTGGA T C CENPU Ensembl:ENSG00000151725 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs559582998 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17811 41846 RMVar_ID_41846 Human_SNP_ID_217092223 A-to-I Human chr4 - 184699208 184699208 184699208 CTCCTGCCTCATCCTCCCGAATAGTTGGGACTACAGGCGCCTGCCACTGTGCCCGGCTAATTTTT CTCCTGCCTCATCCTCCCGAATAGTTGGGACTTCAGGCGCCTGCCACTGTGCCCGGCTAATTTTT T A CENPU Ensembl:ENSG00000151725 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs901093610 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17811 41847 RMVar_ID_41847 Human_SNP_ID_217092249 A-to-I Human chr4 - 184699283 184699283 184699283 CTCTGTCGCCCAGGCTGGAGTGCGGTGGCGCTATCTTGGCTCACTGCAAGCTCCGCCTCCCGGGT CTCTGTCGCCCAGGCTGGAGTGCGGTGGCGCTTTCTTGGCTCACTGCAAGCTCCGCCTCCCGGGT T A CENPU Ensembl:ENSG00000151725 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1169543466 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17811 41848 RMVar_ID_41848 Human_SNP_ID_217092264 A-to-I Human chr4 - 184699326 184699326 184699326 TTTATTTATTTATTTATTTATTTATTTTTGAGACGGAGTCTGGCTCTGTCGCCCAGGCTGGAGTG TTTATTTATTTATTTATTTATTTATTTTTGAGGCGGAGTCTGGCTCTGTCGCCCAGGCTGGAGTG T C CENPU Ensembl:ENSG00000151725 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1166818827 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7294331 RMVar_hsa_circ_17811 41849 RMVar_ID_41849 Human_SNP_ID_217092391 A-to-I Human chr4 - 184699696 184699695 184699697 AGATTGTGCCAGTGCACTCCAGCCTGGGTGACAGAGTGAAACTGTGTCTCAAAAAAAAAAGAGAG AGATTGTGCCAGTGCACTCCAGCCTGGGTGA__GAGTGAAACTGTGTCTCAAAAAAAAAAGAGAG CTG C CENPU Ensembl:ENSG00000151725 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1224128944 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_17811 41850 RMVar_ID_41850 Human_SNP_ID_217112852 A-to-I Human chr4 - 184781069 184781069 184781069 CCACCATGCCTGGCTAATTTTTTATTTTCAGTAGAGACGGGGTTTTACCATGTTGGCCAGGCTGG CCACCATGCCTGGCTAATTTTTTATTTTCAGTGGAGACGGGGTTTTACCATGTTGGCCAGGCTGG T C ACSL1 Ensembl:ENSG00000151726 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs181056475 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33955,RMVar_hsa_circ_73945,RMVar_hsa_circ_56437,RMVar_hsa_circ_69387,RMVar_hsa_circ_229800,RMVar_hsa_circ_344114,RMVar_hsa_circ_351352,RMVar_hsa_circ_282288,RMVar_hsa_circ_229799 41851 RMVar_ID_41851 Human_SNP_ID_217112860 A-to-I Human chr4 - 184781112 184781112 184781112 ATTCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGTTTCACGCCACCATGCCTGGCTAATTTTT ATTCTGCCTCAGCCTCCTGAGTAGCTGGGATTGCAGTTTCACGCCACCATGCCTGGCTAATTTTT T C ACSL1 Ensembl:ENSG00000151726 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1180449768 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33955,RMVar_hsa_circ_73945,RMVar_hsa_circ_56437,RMVar_hsa_circ_69387,RMVar_hsa_circ_229800,RMVar_hsa_circ_344114,RMVar_hsa_circ_351352,RMVar_hsa_circ_282288,RMVar_hsa_circ_229799 41852 RMVar_ID_41852 Human_SNP_ID_217113481 A-to-I Human chr4 - 184783436 184783436 184783436 CCTGCAGCCTCTTGTGTAGGCTTTCCTAGTGCATGCTGCTGACCCTCAAAGCTGTCCTTGGCCAA CCTGCAGCCTCTTGTGTAGGCTTTCCTAGTGCGTGCTGCTGACCCTCAAAGCTGTCCTTGGCCAA T C ACSL1 Ensembl:ENSG00000151726 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1968957 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33955,RMVar_hsa_circ_73945,RMVar_hsa_circ_56437,RMVar_hsa_circ_69387,RMVar_hsa_circ_229800,RMVar_hsa_circ_344114,RMVar_hsa_circ_351352,RMVar_hsa_circ_282288,RMVar_hsa_circ_229799 41853 RMVar_ID_41853 Human_SNP_ID_217113482 A-to-I Human chr4 - 184783436 184783436 184783436 CCTGCAGCCTCTTGTGTAGGCTTTCCTAGTGCATGCTGCTGACCCTCAAAGCTGTCCTTGGCCAA CCTGCAGCCTCTTGTGTAGGCTTTCCTAGTGCCTGCTGCTGACCCTCAAAGCTGTCCTTGGCCAA T G ACSL1 Ensembl:ENSG00000151726 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1968957 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33955,RMVar_hsa_circ_73945,RMVar_hsa_circ_56437,RMVar_hsa_circ_69387,RMVar_hsa_circ_229800,RMVar_hsa_circ_344114,RMVar_hsa_circ_351352,RMVar_hsa_circ_282288,RMVar_hsa_circ_229799 41854 RMVar_ID_41854 Human_SNP_ID_217207929 A-to-I Human chr4 + 185146343 185146343 185146343 TCTGTTGTGCCAGAGAAAGTTTTGGCTTCTATAGGTTGAACCATACGAAATTGCCACTTTAAAAG TCTGTTGTGCCAGAGAAAGTTTTGGCTTCTATGGGTTGAACCATACGAAATTGCCACTTTAAAAG A G SLC25A4 Ensembl:ENSG00000151729 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs981638391 Functional Loss SNV dbSNP153 33..33 33 - - - 41855 RMVar_ID_41855 Human_SNP_ID_217211452 A-to-I Human chr4 - 185160851 185160851 185160851 TTTATTTTAAAAATCTTTTAAAAAAGATTTTTATATATATATAAAGATTATATATTTATATATAG TTTATTTTAAAAATCTTTTAAAAAAGATTTTTTTATATATATAAAGATTATATATTTATATATAG T A CFAP97 Ensembl:ENSG00000164323 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs899395157 Functional Loss SNV dbSNP153 33..33 33 - - - 41856 RMVar_ID_41856 Human_SNP_ID_217211453 A-to-I Human chr4 - 185160851 185160851 185160851 TTTATTTTAAAAATCTTTTAAAAAAGATTTTTATATATATATAAAGATTATATATTTATATATAG TTTATTTTAAAAATCTTTTAAAAAAGATTTTTGTATATATATAAAGATTATATATTTATATATAG T C CFAP97 Ensembl:ENSG00000164323 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs899395157 Functional Loss SNV dbSNP153 33..33 33 - - - 41857 RMVar_ID_41857 Human_SNP_ID_217211456 A-to-I Human chr4 - 185160861 185160858 185160861 TTTTATAAATTTTATTTTAAAAATCTTTTAAAAAAGATTTTTATATATATATAAAGATTATATAT TTTTATAAATTTTATTTTAAAAATCTTTTAAA___GATTTTTATATATATATAAAGATTATATAT CTTT C CFAP97 Ensembl:ENSG00000164323 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1050553236 Functional Loss DEL dbSNP153 33..35 33 - - - 41858 RMVar_ID_41858 Human_SNP_ID_217211457 A-to-I Human chr4 - 185160861 185160858 185160861 TTTTATAAATTTTATTTTAAAAATCTTTTAAAAAAGATTTTTATATATATATAAAGATTATATAT TTTTATAAATTTTATTTTAAAAATCTTTTAAA_AAGATTTTTATATATATATAAAGATTATATAT CTTT CTT CFAP97 Ensembl:ENSG00000164323 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1050553236 Functional Loss DEL dbSNP153 33..33 33 - - - 41859 RMVar_ID_41859 Human_SNP_ID_217211458 A-to-I Human chr4 - 185160861 185160861 185160861 TTTTATAAATTTTATTTTAAAAATCTTTTAAAAAAGATTTTTATATATATATAAAGATTATATAT TTTTATAAATTTTATTTTAAAAATCTTTTAAAGAAGATTTTTATATATATATAAAGATTATATAT T C CFAP97 Ensembl:ENSG00000164323 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs371123345 Functional Loss SNV dbSNP153 33..33 33 - - - 41860 RMVar_ID_41860 Human_SNP_ID_217211459 A-to-I Human chr4 - 185160862 185160862 185160862 TTTTTATAAATTTTATTTTAAAAATCTTTTAAAAAAGATTTTTATATATATATAAAGATTATATA TTTTTATAAATTTTATTTTAAAAATCTTTTAAGAAAGATTTTTATATATATATAAAGATTATATA T C CFAP97 Ensembl:ENSG00000164323 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs534925149 Functional Loss SNV dbSNP153 33..33 33 - - - 41861 RMVar_ID_41861 Human_SNP_ID_217223874 A-to-I Human chr4 - 185207355 185207352 185207356 AAAATTAACCAGGTGTGGTGGTGTGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTAACCAGGTGTGGTGGTGTGCGCCTG____CCCAGCTACTCGGGAGGCTGAGGCAGGAGA GACTA G CFAP97 Ensembl:ENSG00000164323 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1483586581 Functional Loss DEL dbSNP153 32..35 33 - - - 41862 RMVar_ID_41862 Human_SNP_ID_217223876 A-to-I Human chr4 - 185207355 185207355 185207355 AAAATTAACCAGGTGTGGTGGTGTGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTAACCAGGTGTGGTGGTGTGCGCCTGTGGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA T C CFAP97 Ensembl:ENSG00000164323 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1209280470 Functional Loss SNV dbSNP153 33..33 33 - - - 41863 RMVar_ID_41863 Human_SNP_ID_217224103 A-to-I Human chr4 - 185208217 185208217 185208217 AGTTAGGAGTTCAAGACTAGCCTGGCCAACATAGTGAAACTTGAACCCCGGAGGTGGAGGTCGCA AGTTAGGAGTTCAAGACTAGCCTGGCCAACATGGTGAAACTTGAACCCCGGAGGTGGAGGTCGCA T C CFAP97 Ensembl:ENSG00000164323 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1050482088 Functional Loss SNV dbSNP153 33..33 33 - - - 41864 RMVar_ID_41864 Human_SNP_ID_217226332 A-to-I Human chr4 + 185215997 185215997 185215997 TTTTGTATTTTTGGTAGAGACGGGGTTTTGCTATGTTGCCCAGGCTGGTCTCAGATTTCTGAGCT TTTTGTATTTTTGGTAGAGACGGGGTTTTGCTGTGTTGCCCAGGCTGGTCTCAGATTTCTGAGCT A G SNX25 Ensembl:ENSG00000109762 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs943591842 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93131,RMVar_hsa_circ_229811 41865 RMVar_ID_41865 Human_SNP_ID_217226508 A-to-I Human chr4 + 185216589 185216589 185216589 TTGCCCAGGCTGGAGTGCAGTGGCACAATCTCAGCTCACTGTAACTTCTGTTTCCTGGGTTCAAG TTGCCCAGGCTGGAGTGCAGTGGCACAATCTCGGCTCACTGTAACTTCTGTTTCCTGGGTTCAAG A G SNX25 Ensembl:ENSG00000109762 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1336960992 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93131,RMVar_hsa_circ_229811 41866 RMVar_ID_41866 Human_SNP_ID_217226761 A-to-I Human chr4 + 185217533 185217533 185217533 GAAAGTCTTCCAAGTTGAATGTTCTACTTGGCACCTTCTTAATTCTGGTCATTCCCAGGGGATTT GAAAGTCTTCCAAGTTGAATGTTCTACTTGGCGCCTTCTTAATTCTGGTCATTCCCAGGGGATTT A G SNX25 Ensembl:ENSG00000109762 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs3108291 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24048447 GWAS_ID_4805,GWAS_ID_4806,GWAS_ID_4807,GWAS_ID_4808,GWAS_ID_4809,GWAS_ID_4810,GWAS_ID_4811,GWAS_ID_4812,GWAS_ID_4813,GWAS_ID_4814,GWAS_ID_4815,GWAS_ID_4816,GWAS_ID_4817,GWAS_ID_4818,GWAS_ID_4819,GWAS_ID_4820,GWAS_ID_4821,GWAS_ID_4822,GWAS_ID_4823,GWAS_ID_4824,GWAS_ID_4825,GWAS_ID_4826,GWAS_ID_4827,GWAS_ID_4828,GWAS_ID_4829,GWAS_ID_4830,GWAS_ID_4831,GWAS_ID_4832,GWAS_ID_4833,GWAS_ID_4834,GWAS_ID_4835,GWAS_ID_4836,GWAS_ID_4837,GWAS_ID_4838,GWAS_ID_4839,GWAS_ID_4840,GWAS_ID_4841,GWAS_ID_4842,GWAS_ID_4843,GWAS_ID_4844,GWAS_ID_4845,GWAS_ID_4846,GWAS_ID_4847,GWAS_ID_4848,GWAS_ID_4849,GWAS_ID_4850,GWAS_ID_4851,GWAS_ID_4852,GWAS_ID_4853,GWAS_ID_4854,GWAS_ID_4855,GWAS_ID_4856,GWAS_ID_4857,GWAS_ID_4858,GWAS_ID_4859,GWAS_ID_4860,GWAS_ID_4861,GWAS_ID_4862,GWAS_ID_4863,GWAS_ID_4864,GWAS_ID_4865,GWAS_ID_4866,GWAS_ID_4867,GWAS_ID_4868,GWAS_ID_4869,GWAS_ID_4870,GWAS_ID_4871,GWAS_ID_4872 RMVar_hsa_circ_93131,RMVar_hsa_circ_229811 41867 RMVar_ID_41867 Human_SNP_ID_217227510 A-to-I Human chr4 + 185220585 185220585 185220585 CTTACTACAACCTCTGCCTGCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGG CTTACTACAACCTCTGCCTGCCAGGTTCAAGCCATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGG A C SNX25 Ensembl:ENSG00000109762 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1235607870 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93131,RMVar_hsa_circ_229811 41868 RMVar_ID_41868 Human_SNP_ID_217228377 A-to-I Human chr4 + 185223177 185223177 185223177 ATCAGCACCTTCTCTCCCACCTTAGCAACCTCATCTTGACTTTATAGGAATCACTTCCTTGCATG ATCAGCACCTTCTCTCCCACCTTAGCAACCTCGTCTTGACTTTATAGGAATCACTTCCTTGCATG A G SNX25 Ensembl:ENSG00000109762 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs3112903 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_4873,GWAS_ID_4874,GWAS_ID_4875,GWAS_ID_4876,GWAS_ID_4877,GWAS_ID_4878,GWAS_ID_4879,GWAS_ID_4880,GWAS_ID_4881,GWAS_ID_4882,GWAS_ID_4883,GWAS_ID_4884,GWAS_ID_4885,GWAS_ID_4886,GWAS_ID_4887,GWAS_ID_4888,GWAS_ID_4889,GWAS_ID_4890,GWAS_ID_4891,GWAS_ID_4892,GWAS_ID_4893,GWAS_ID_4894,GWAS_ID_4895,GWAS_ID_4896,GWAS_ID_4897,GWAS_ID_4898,GWAS_ID_4899,GWAS_ID_4900,GWAS_ID_4901,GWAS_ID_4902,GWAS_ID_4903,GWAS_ID_4904,GWAS_ID_4905,GWAS_ID_4906,GWAS_ID_4907,GWAS_ID_4908,GWAS_ID_4909,GWAS_ID_4910,GWAS_ID_4911,GWAS_ID_4912,GWAS_ID_4913,GWAS_ID_4914,GWAS_ID_4915,GWAS_ID_4916,GWAS_ID_4917,GWAS_ID_4918,GWAS_ID_4919,GWAS_ID_4920,GWAS_ID_4921,GWAS_ID_4922,GWAS_ID_4923,GWAS_ID_4924,GWAS_ID_4925,GWAS_ID_4926,GWAS_ID_4927,GWAS_ID_4928,GWAS_ID_4929,GWAS_ID_4930,GWAS_ID_4931,GWAS_ID_4932,GWAS_ID_4933,GWAS_ID_4934,GWAS_ID_4935,GWAS_ID_4936,GWAS_ID_4937,GWAS_ID_4938,GWAS_ID_4939,GWAS_ID_4940,GWAS_ID_4941,GWAS_ID_4942,GWAS_ID_4943,GWAS_ID_4944,GWAS_ID_4945 RMVar_hsa_circ_93131,RMVar_hsa_circ_229811 41869 RMVar_ID_41869 Human_SNP_ID_217228648 A-to-I Human chr4 + 185224189 185224189 185224189 GCCTGGACAACATGGTGAAACCTGTCTCTACTAGAAATACAAAAAATTAGCTGGGCATGGTGGCG GCCTGGACAACATGGTGAAACCTGTCTCTACTGGAAATACAAAAAATTAGCTGGGCATGGTGGCG A G SNX25 Ensembl:ENSG00000109762 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1397985135 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7294718 RMVar_hsa_circ_93131,RMVar_hsa_circ_229811 41870 RMVar_ID_41870 Human_SNP_ID_217234477 A-to-I Human chr4 + 185244032 185244032 185244032 TTTCTTTCTTTTTTTTGAGACAGTGTCTTGCTATGTTGCCCAGGCTGGAGTGCAGTGGTGCAGTC TTTCTTTCTTTTTTTTGAGACAGTGTCTTGCTGTGTTGCCCAGGCTGGAGTGCAGTGGTGCAGTC A G SNX25 Ensembl:ENSG00000109762 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1473578801 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93131,RMVar_hsa_circ_229811 41871 RMVar_ID_41871 Human_SNP_ID_217234858 A-to-I Human chr4 + 185245607 185245607 185245607 GTGATCCACCAGCCTCGGCCTCCCAAAGTGCTAGGATTATAAGCGTAAGCCACTGCACCCAGCCC GTGATCCACCAGCCTCGGCCTCCCAAAGTGCTGGGATTATAAGCGTAAGCCACTGCACCCAGCCC A G SNX25 Ensembl:ENSG00000109762 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs900812721 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93131,RMVar_hsa_circ_229811 41872 RMVar_ID_41872 Human_SNP_ID_217243310 A-to-I Human chr4 + 185281889 185281889 185281889 AATACAAAAATTAGCCGGGTATGGTCGTGCGCACCTGTAATCCCAGCTATTCCAGAGGCTGAGAC AATACAAAAATTAGCCGGGTATGGTCGTGCGCTCCTGTAATCCCAGCTATTCCAGAGGCTGAGAC A T SNX25 Ensembl:ENSG00000109762 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1249421607 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55589,RMVar_hsa_circ_54915,RMVar_hsa_circ_117822,RMVar_hsa_circ_329071,RMVar_hsa_circ_346452,RMVar_hsa_circ_340568,RMVar_hsa_circ_315051,RMVar_hsa_circ_270984,RMVar_hsa_circ_92358,RMVar_hsa_circ_109238,RMVar_hsa_circ_75720,RMVar_hsa_circ_117752,RMVar_hsa_circ_229815,RMVar_hsa_circ_229819,RMVar_hsa_circ_229817,RMVar_hsa_circ_229818,RMVar_hsa_circ_229816,RMVar_hsa_circ_229813,RMVar_hsa_circ_229814,RMVar_hsa_circ_333481,RMVar_hsa_circ_229812,RMVar_hsa_circ_373593,RMVar_hsa_circ_98895,RMVar_hsa_circ_101722,RMVar_hsa_circ_97956,RMVar_hsa_circ_113200,RMVar_hsa_circ_229824,RMVar_hsa_circ_229826,RMVar_hsa_circ_229828,RMVar_hsa_circ_229827,RMVar_hsa_circ_229825,RMVar_hsa_circ_322595,RMVar_hsa_circ_120585,RMVar_hsa_circ_83868,RMVar_hsa_circ_229832,RMVar_hsa_circ_229833,RMVar_hsa_circ_229831 41873 RMVar_ID_41873 Human_SNP_ID_217250514 A-to-I Human chr4 + 185312589 185312589 185312589 CTGTCGCCCAGGCTGGCATGCATTGGCGCGATATCGGCTCACTGCAACCTCCACCTCCCGGGTTC CTGTCGCCCAGGCTGGCATGCATTGGCGCGATGTCGGCTCACTGCAACCTCCACCTCCCGGGTTC A G SNX25 Ensembl:ENSG00000109762 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1560999610 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54915,RMVar_hsa_circ_117822,RMVar_hsa_circ_329071,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_229817,RMVar_hsa_circ_229816,RMVar_hsa_circ_229813,RMVar_hsa_circ_229814,RMVar_hsa_circ_229812,RMVar_hsa_circ_373593,RMVar_hsa_circ_98895,RMVar_hsa_circ_101722,RMVar_hsa_circ_97956,RMVar_hsa_circ_41340,RMVar_hsa_circ_113200,RMVar_hsa_circ_229824,RMVar_hsa_circ_229826,RMVar_hsa_circ_229828,RMVar_hsa_circ_229827,RMVar_hsa_circ_229825,RMVar_hsa_circ_83868,RMVar_hsa_circ_229832,RMVar_hsa_circ_229833,RMVar_hsa_circ_363695,RMVar_hsa_circ_368677,RMVar_hsa_circ_75936,RMVar_hsa_circ_51145,RMVar_hsa_circ_26323,RMVar_hsa_circ_34430,RMVar_hsa_circ_229834,RMVar_hsa_circ_229835,RMVar_hsa_circ_284015,RMVar_hsa_circ_291046 41874 RMVar_ID_41874 Human_SNP_ID_217250533 A-to-I Human chr4 + 185312662 185312661 185312663 CTCCTGCCTCAGCCTCCCGAGCAGCTGGGACTACAGACGCCCGCCACCACACCCAGCTAAATTTT CTCCTGCCTCAGCCTCCCGAGCAGCTGGGACT__AGACGCCCGCCACCACACCCAGCTAAATTTT TAC T SNX25 Ensembl:ENSG00000109762 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs112326227 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_54915,RMVar_hsa_circ_117822,RMVar_hsa_circ_329071,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_229817,RMVar_hsa_circ_229816,RMVar_hsa_circ_229813,RMVar_hsa_circ_229814,RMVar_hsa_circ_229812,RMVar_hsa_circ_373593,RMVar_hsa_circ_98895,RMVar_hsa_circ_101722,RMVar_hsa_circ_97956,RMVar_hsa_circ_41340,RMVar_hsa_circ_113200,RMVar_hsa_circ_229824,RMVar_hsa_circ_229826,RMVar_hsa_circ_229828,RMVar_hsa_circ_229827,RMVar_hsa_circ_229825,RMVar_hsa_circ_83868,RMVar_hsa_circ_229832,RMVar_hsa_circ_229833,RMVar_hsa_circ_363695,RMVar_hsa_circ_368677,RMVar_hsa_circ_75936,RMVar_hsa_circ_51145,RMVar_hsa_circ_26323,RMVar_hsa_circ_34430,RMVar_hsa_circ_229834,RMVar_hsa_circ_229835,RMVar_hsa_circ_284015,RMVar_hsa_circ_291046 41875 RMVar_ID_41875 Human_SNP_ID_217250565 A-to-I Human chr4 + 185312799 185312799 185312799 TGCCCACCTCAGCATTCCAGTGTGTTGGGATTACAGGCGTGAGCCACTGCGCCTGGCCTTGATTT TGCCCACCTCAGCATTCCAGTGTGTTGGGATTTCAGGCGTGAGCCACTGCGCCTGGCCTTGATTT A T SNX25 Ensembl:ENSG00000109762 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017511763 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54915,RMVar_hsa_circ_117822,RMVar_hsa_circ_329071,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_229817,RMVar_hsa_circ_229816,RMVar_hsa_circ_229813,RMVar_hsa_circ_229814,RMVar_hsa_circ_229812,RMVar_hsa_circ_373593,RMVar_hsa_circ_98895,RMVar_hsa_circ_101722,RMVar_hsa_circ_97956,RMVar_hsa_circ_41340,RMVar_hsa_circ_113200,RMVar_hsa_circ_229824,RMVar_hsa_circ_229826,RMVar_hsa_circ_229828,RMVar_hsa_circ_229827,RMVar_hsa_circ_229825,RMVar_hsa_circ_83868,RMVar_hsa_circ_229832,RMVar_hsa_circ_229833,RMVar_hsa_circ_363695,RMVar_hsa_circ_368677,RMVar_hsa_circ_75936,RMVar_hsa_circ_51145,RMVar_hsa_circ_26323,RMVar_hsa_circ_34430,RMVar_hsa_circ_229834,RMVar_hsa_circ_229835,RMVar_hsa_circ_284015,RMVar_hsa_circ_291046 41876 RMVar_ID_41876 Human_SNP_ID_217250963 A-to-I Human chr4 + 185314604 185314604 185314604 AATGGAGGCTGGGCGCAGTGGCTCACGCCTGTAATCCCAACACTTTAGGAGGCTGAGGCAGGCGG AATGGAGGCTGGGCGCAGTGGCTCACGCCTGTGATCCCAACACTTTAGGAGGCTGAGGCAGGCGG A G SNX25 Ensembl:ENSG00000109762 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1029661198 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54915,RMVar_hsa_circ_117822,RMVar_hsa_circ_329071,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_229817,RMVar_hsa_circ_229816,RMVar_hsa_circ_229813,RMVar_hsa_circ_229814,RMVar_hsa_circ_229812,RMVar_hsa_circ_373593,RMVar_hsa_circ_98895,RMVar_hsa_circ_101722,RMVar_hsa_circ_97956,RMVar_hsa_circ_41340,RMVar_hsa_circ_113200,RMVar_hsa_circ_229824,RMVar_hsa_circ_229826,RMVar_hsa_circ_229828,RMVar_hsa_circ_229827,RMVar_hsa_circ_229825,RMVar_hsa_circ_83868,RMVar_hsa_circ_229832,RMVar_hsa_circ_229833,RMVar_hsa_circ_363695,RMVar_hsa_circ_368677,RMVar_hsa_circ_75936,RMVar_hsa_circ_51145,RMVar_hsa_circ_26323,RMVar_hsa_circ_34430,RMVar_hsa_circ_229834,RMVar_hsa_circ_229835,RMVar_hsa_circ_284015,RMVar_hsa_circ_291046 41877 RMVar_ID_41877 Human_SNP_ID_217250969 A-to-I Human chr4 + 185314618 185314618 185314618 GCAGTGGCTCACGCCTGTAATCCCAACACTTTAGGAGGCTGAGGCAGGCGGATCACGAGGTCAAG GCAGTGGCTCACGCCTGTAATCCCAACACTTTGGGAGGCTGAGGCAGGCGGATCACGAGGTCAAG A G SNX25 Ensembl:ENSG00000109762 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1421620005 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54915,RMVar_hsa_circ_117822,RMVar_hsa_circ_329071,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_229817,RMVar_hsa_circ_229816,RMVar_hsa_circ_229813,RMVar_hsa_circ_229814,RMVar_hsa_circ_229812,RMVar_hsa_circ_373593,RMVar_hsa_circ_98895,RMVar_hsa_circ_101722,RMVar_hsa_circ_97956,RMVar_hsa_circ_41340,RMVar_hsa_circ_113200,RMVar_hsa_circ_229824,RMVar_hsa_circ_229826,RMVar_hsa_circ_229828,RMVar_hsa_circ_229827,RMVar_hsa_circ_229825,RMVar_hsa_circ_83868,RMVar_hsa_circ_229832,RMVar_hsa_circ_229833,RMVar_hsa_circ_363695,RMVar_hsa_circ_368677,RMVar_hsa_circ_75936,RMVar_hsa_circ_51145,RMVar_hsa_circ_26323,RMVar_hsa_circ_34430,RMVar_hsa_circ_229834,RMVar_hsa_circ_229835,RMVar_hsa_circ_284015,RMVar_hsa_circ_291046 41878 RMVar_ID_41878 Human_SNP_ID_217250975 A-to-I Human chr4 + 185314631 185314631 185314631 CCTGTAATCCCAACACTTTAGGAGGCTGAGGCAGGCGGATCACGAGGTCAAGAGATCGAGACCAT CCTGTAATCCCAACACTTTAGGAGGCTGAGGCGGGCGGATCACGAGGTCAAGAGATCGAGACCAT A G SNX25 Ensembl:ENSG00000109762 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1413186556 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54915,RMVar_hsa_circ_117822,RMVar_hsa_circ_329071,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_229817,RMVar_hsa_circ_229816,RMVar_hsa_circ_229813,RMVar_hsa_circ_229814,RMVar_hsa_circ_229812,RMVar_hsa_circ_373593,RMVar_hsa_circ_98895,RMVar_hsa_circ_101722,RMVar_hsa_circ_97956,RMVar_hsa_circ_41340,RMVar_hsa_circ_113200,RMVar_hsa_circ_229824,RMVar_hsa_circ_229826,RMVar_hsa_circ_229828,RMVar_hsa_circ_229827,RMVar_hsa_circ_229825,RMVar_hsa_circ_83868,RMVar_hsa_circ_229832,RMVar_hsa_circ_229833,RMVar_hsa_circ_363695,RMVar_hsa_circ_368677,RMVar_hsa_circ_75936,RMVar_hsa_circ_51145,RMVar_hsa_circ_26323,RMVar_hsa_circ_34430,RMVar_hsa_circ_229834,RMVar_hsa_circ_229835,RMVar_hsa_circ_284015,RMVar_hsa_circ_291046 41879 RMVar_ID_41879 Human_SNP_ID_217250997 A-to-I Human chr4 + 185314687 185314687 185314687 CGAGACCATCCTGGCCAACTTGGTGACACCCCATCTCTACTAAAAATACAAAAATTAGCTGGGAG CGAGACCATCCTGGCCAACTTGGTGACACCCCGTCTCTACTAAAAATACAAAAATTAGCTGGGAG A G SNX25 Ensembl:ENSG00000109762 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1261099857 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54915,RMVar_hsa_circ_117822,RMVar_hsa_circ_329071,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_229817,RMVar_hsa_circ_229816,RMVar_hsa_circ_229813,RMVar_hsa_circ_229814,RMVar_hsa_circ_229812,RMVar_hsa_circ_373593,RMVar_hsa_circ_98895,RMVar_hsa_circ_101722,RMVar_hsa_circ_97956,RMVar_hsa_circ_41340,RMVar_hsa_circ_113200,RMVar_hsa_circ_229824,RMVar_hsa_circ_229826,RMVar_hsa_circ_229828,RMVar_hsa_circ_229827,RMVar_hsa_circ_229825,RMVar_hsa_circ_83868,RMVar_hsa_circ_229832,RMVar_hsa_circ_229833,RMVar_hsa_circ_363695,RMVar_hsa_circ_368677,RMVar_hsa_circ_75936,RMVar_hsa_circ_51145,RMVar_hsa_circ_26323,RMVar_hsa_circ_34430,RMVar_hsa_circ_229834,RMVar_hsa_circ_229835,RMVar_hsa_circ_284015,RMVar_hsa_circ_291046 41880 RMVar_ID_41880 Human_SNP_ID_217251009 A-to-I Human chr4 + 185314735 185314735 185314735 CAAAAATTAGCTGGGAGTGGTGGTGGGCACCTATAATCCCAGGTACTCGGGAGGCTGCGGCAGAA CAAAAATTAGCTGGGAGTGGTGGTGGGCACCTGTAATCCCAGGTACTCGGGAGGCTGCGGCAGAA A G SNX25 Ensembl:ENSG00000109762 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs113204110 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54915,RMVar_hsa_circ_117822,RMVar_hsa_circ_329071,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_229817,RMVar_hsa_circ_229816,RMVar_hsa_circ_229813,RMVar_hsa_circ_229814,RMVar_hsa_circ_229812,RMVar_hsa_circ_373593,RMVar_hsa_circ_98895,RMVar_hsa_circ_101722,RMVar_hsa_circ_97956,RMVar_hsa_circ_41340,RMVar_hsa_circ_113200,RMVar_hsa_circ_229824,RMVar_hsa_circ_229826,RMVar_hsa_circ_229828,RMVar_hsa_circ_229827,RMVar_hsa_circ_229825,RMVar_hsa_circ_83868,RMVar_hsa_circ_229832,RMVar_hsa_circ_229833,RMVar_hsa_circ_363695,RMVar_hsa_circ_368677,RMVar_hsa_circ_75936,RMVar_hsa_circ_51145,RMVar_hsa_circ_26323,RMVar_hsa_circ_34430,RMVar_hsa_circ_229834,RMVar_hsa_circ_229835,RMVar_hsa_circ_284015,RMVar_hsa_circ_291046 41881 RMVar_ID_41881 Human_SNP_ID_217251035 A-to-I Human chr4 + 185314827 185314827 185314827 TTGCAGTGAGCCGAGATCACGCCACTGCACTCAAGCCTGGCGACAAAGTGAGACTCTGTCTCAAA TTGCAGTGAGCCGAGATCACGCCACTGCACTCCAGCCTGGCGACAAAGTGAGACTCTGTCTCAAA A C SNX25 Ensembl:ENSG00000109762 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1284229893 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54915,RMVar_hsa_circ_117822,RMVar_hsa_circ_329071,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_229817,RMVar_hsa_circ_229816,RMVar_hsa_circ_229813,RMVar_hsa_circ_229814,RMVar_hsa_circ_229812,RMVar_hsa_circ_373593,RMVar_hsa_circ_98895,RMVar_hsa_circ_101722,RMVar_hsa_circ_97956,RMVar_hsa_circ_41340,RMVar_hsa_circ_113200,RMVar_hsa_circ_229824,RMVar_hsa_circ_229826,RMVar_hsa_circ_229828,RMVar_hsa_circ_229827,RMVar_hsa_circ_229825,RMVar_hsa_circ_83868,RMVar_hsa_circ_229832,RMVar_hsa_circ_229833,RMVar_hsa_circ_363695,RMVar_hsa_circ_368677,RMVar_hsa_circ_75936,RMVar_hsa_circ_51145,RMVar_hsa_circ_26323,RMVar_hsa_circ_34430,RMVar_hsa_circ_229834,RMVar_hsa_circ_229835,RMVar_hsa_circ_284015,RMVar_hsa_circ_291046 41882 RMVar_ID_41882 Human_SNP_ID_217251089 A-to-I Human chr4 + 185314965 185314965 185314965 TCTAAAACCTTCCCGGCTGGGCGCGGTGGCTCACGCCTGTAGTCCCAGCACTTTGGGAGGCCGAG TCTAAAACCTTCCCGGCTGGGCGCGGTGGCTCGCGCCTGTAGTCCCAGCACTTTGGGAGGCCGAG A G SNX25 Ensembl:ENSG00000109762 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs971501440 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_160381 RMVar_hsa_circ_54915,RMVar_hsa_circ_117822,RMVar_hsa_circ_329071,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_229817,RMVar_hsa_circ_229816,RMVar_hsa_circ_229813,RMVar_hsa_circ_229814,RMVar_hsa_circ_229812,RMVar_hsa_circ_373593,RMVar_hsa_circ_98895,RMVar_hsa_circ_101722,RMVar_hsa_circ_97956,RMVar_hsa_circ_41340,RMVar_hsa_circ_113200,RMVar_hsa_circ_229824,RMVar_hsa_circ_229826,RMVar_hsa_circ_229828,RMVar_hsa_circ_229827,RMVar_hsa_circ_229825,RMVar_hsa_circ_83868,RMVar_hsa_circ_229832,RMVar_hsa_circ_229833,RMVar_hsa_circ_363695,RMVar_hsa_circ_368677,RMVar_hsa_circ_75936,RMVar_hsa_circ_51145,RMVar_hsa_circ_26323,RMVar_hsa_circ_34430,RMVar_hsa_circ_229834,RMVar_hsa_circ_229835,RMVar_hsa_circ_284015,RMVar_hsa_circ_291046 41883 RMVar_ID_41883 Human_SNP_ID_217251093 A-to-I Human chr4 + 185314973 185314973 185314973 CTTCCCGGCTGGGCGCGGTGGCTCACGCCTGTAGTCCCAGCACTTTGGGAGGCCGAGGCGGGCGG CTTCCCGGCTGGGCGCGGTGGCTCACGCCTGTCGTCCCAGCACTTTGGGAGGCCGAGGCGGGCGG A C SNX25 Ensembl:ENSG00000109762 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs371192747 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_160381 RMVar_hsa_circ_54915,RMVar_hsa_circ_117822,RMVar_hsa_circ_329071,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_229817,RMVar_hsa_circ_229816,RMVar_hsa_circ_229813,RMVar_hsa_circ_229814,RMVar_hsa_circ_229812,RMVar_hsa_circ_373593,RMVar_hsa_circ_98895,RMVar_hsa_circ_101722,RMVar_hsa_circ_97956,RMVar_hsa_circ_41340,RMVar_hsa_circ_113200,RMVar_hsa_circ_229824,RMVar_hsa_circ_229826,RMVar_hsa_circ_229828,RMVar_hsa_circ_229827,RMVar_hsa_circ_229825,RMVar_hsa_circ_83868,RMVar_hsa_circ_229832,RMVar_hsa_circ_229833,RMVar_hsa_circ_363695,RMVar_hsa_circ_368677,RMVar_hsa_circ_75936,RMVar_hsa_circ_51145,RMVar_hsa_circ_26323,RMVar_hsa_circ_34430,RMVar_hsa_circ_229834,RMVar_hsa_circ_229835,RMVar_hsa_circ_284015,RMVar_hsa_circ_291046 41884 RMVar_ID_41884 Human_SNP_ID_217251183 A-to-I Human chr4 + 185315212 185315212 185315212 ATTGTGCCACTGCACTCCAGCCTCAGAGACAGAGCAAGACTCCATCTCAAAAAAAAAGAAAAGAA ATTGTGCCACTGCACTCCAGCCTCAGAGACAGGGCAAGACTCCATCTCAAAAAAAAAGAAAAGAA A G SNX25 Ensembl:ENSG00000109762 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1278664769 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54915,RMVar_hsa_circ_117822,RMVar_hsa_circ_329071,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_229817,RMVar_hsa_circ_229816,RMVar_hsa_circ_229813,RMVar_hsa_circ_229814,RMVar_hsa_circ_229812,RMVar_hsa_circ_373593,RMVar_hsa_circ_98895,RMVar_hsa_circ_101722,RMVar_hsa_circ_97956,RMVar_hsa_circ_41340,RMVar_hsa_circ_113200,RMVar_hsa_circ_229824,RMVar_hsa_circ_229826,RMVar_hsa_circ_229828,RMVar_hsa_circ_229827,RMVar_hsa_circ_229825,RMVar_hsa_circ_83868,RMVar_hsa_circ_229832,RMVar_hsa_circ_229833,RMVar_hsa_circ_363695,RMVar_hsa_circ_368677,RMVar_hsa_circ_75936,RMVar_hsa_circ_51145,RMVar_hsa_circ_26323,RMVar_hsa_circ_34430,RMVar_hsa_circ_229834,RMVar_hsa_circ_229835,RMVar_hsa_circ_284015,RMVar_hsa_circ_291046 41885 RMVar_ID_41885 Human_SNP_ID_217251184 A-to-I Human chr4 + 185315215 185315215 185315215 GTGCCACTGCACTCCAGCCTCAGAGACAGAGCAAGACTCCATCTCAAAAAAAAAGAAAAGAAAAG GTGCCACTGCACTCCAGCCTCAGAGACAGAGCGAGACTCCATCTCAAAAAAAAAGAAAAGAAAAG A G SNX25 Ensembl:ENSG00000109762 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1200950224 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54915,RMVar_hsa_circ_117822,RMVar_hsa_circ_329071,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_229817,RMVar_hsa_circ_229816,RMVar_hsa_circ_229813,RMVar_hsa_circ_229814,RMVar_hsa_circ_229812,RMVar_hsa_circ_373593,RMVar_hsa_circ_98895,RMVar_hsa_circ_101722,RMVar_hsa_circ_97956,RMVar_hsa_circ_41340,RMVar_hsa_circ_113200,RMVar_hsa_circ_229824,RMVar_hsa_circ_229826,RMVar_hsa_circ_229828,RMVar_hsa_circ_229827,RMVar_hsa_circ_229825,RMVar_hsa_circ_83868,RMVar_hsa_circ_229832,RMVar_hsa_circ_229833,RMVar_hsa_circ_363695,RMVar_hsa_circ_368677,RMVar_hsa_circ_75936,RMVar_hsa_circ_51145,RMVar_hsa_circ_26323,RMVar_hsa_circ_34430,RMVar_hsa_circ_229834,RMVar_hsa_circ_229835,RMVar_hsa_circ_284015,RMVar_hsa_circ_291046 41886 RMVar_ID_41886 Human_SNP_ID_217251226 A-to-I Human chr4 + 185315313 185315311 185315313 TTTCACTGGTGATTTTTTTTTTTTTTTTTTTGAGGTGGAGTCTTCCTCTGTTGTTCAGGCTGGAG TTTCACTGGTGATTTTTTTTTTTTTTTTTTT__GGTGGAGTCTTCCTCTGTTGTTCAGGCTGGAG TGA T SNX25 Ensembl:ENSG00000109762 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1325154695 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_54915,RMVar_hsa_circ_117822,RMVar_hsa_circ_329071,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_229817,RMVar_hsa_circ_229816,RMVar_hsa_circ_229813,RMVar_hsa_circ_229814,RMVar_hsa_circ_229812,RMVar_hsa_circ_373593,RMVar_hsa_circ_98895,RMVar_hsa_circ_101722,RMVar_hsa_circ_97956,RMVar_hsa_circ_41340,RMVar_hsa_circ_113200,RMVar_hsa_circ_229824,RMVar_hsa_circ_229826,RMVar_hsa_circ_229828,RMVar_hsa_circ_229827,RMVar_hsa_circ_229825,RMVar_hsa_circ_83868,RMVar_hsa_circ_229832,RMVar_hsa_circ_229833,RMVar_hsa_circ_363695,RMVar_hsa_circ_368677,RMVar_hsa_circ_75936,RMVar_hsa_circ_51145,RMVar_hsa_circ_26323,RMVar_hsa_circ_34430,RMVar_hsa_circ_229834,RMVar_hsa_circ_229835,RMVar_hsa_circ_284015,RMVar_hsa_circ_291046 41887 RMVar_ID_41887 Human_SNP_ID_217251229 A-to-I Human chr4 + 185315313 185315313 185315313 TTTCACTGGTGATTTTTTTTTTTTTTTTTTTGAGGTGGAGTCTTCCTCTGTTGTTCAGGCTGGAG TTTCACTGGTGATTTTTTTTTTTTTTTTTTTGGGGTGGAGTCTTCCTCTGTTGTTCAGGCTGGAG A G SNX25 Ensembl:ENSG00000109762 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1288381910 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54915,RMVar_hsa_circ_117822,RMVar_hsa_circ_329071,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_229817,RMVar_hsa_circ_229816,RMVar_hsa_circ_229813,RMVar_hsa_circ_229814,RMVar_hsa_circ_229812,RMVar_hsa_circ_373593,RMVar_hsa_circ_98895,RMVar_hsa_circ_101722,RMVar_hsa_circ_97956,RMVar_hsa_circ_41340,RMVar_hsa_circ_113200,RMVar_hsa_circ_229824,RMVar_hsa_circ_229826,RMVar_hsa_circ_229828,RMVar_hsa_circ_229827,RMVar_hsa_circ_229825,RMVar_hsa_circ_83868,RMVar_hsa_circ_229832,RMVar_hsa_circ_229833,RMVar_hsa_circ_363695,RMVar_hsa_circ_368677,RMVar_hsa_circ_75936,RMVar_hsa_circ_51145,RMVar_hsa_circ_26323,RMVar_hsa_circ_34430,RMVar_hsa_circ_229834,RMVar_hsa_circ_229835,RMVar_hsa_circ_284015,RMVar_hsa_circ_291046 41888 RMVar_ID_41888 Human_SNP_ID_217251230 A-to-I Human chr4 + 185315313 185315313 185315313 TTTCACTGGTGATTTTTTTTTTTTTTTTTTTGAGGTGGAGTCTTCCTCTGTTGTTCAGGCTGGAG TTTCACTGGTGATTTTTTTTTTTTTTTTTTTGTGGTGGAGTCTTCCTCTGTTGTTCAGGCTGGAG A T SNX25 Ensembl:ENSG00000109762 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1288381910 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54915,RMVar_hsa_circ_117822,RMVar_hsa_circ_329071,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_229817,RMVar_hsa_circ_229816,RMVar_hsa_circ_229813,RMVar_hsa_circ_229814,RMVar_hsa_circ_229812,RMVar_hsa_circ_373593,RMVar_hsa_circ_98895,RMVar_hsa_circ_101722,RMVar_hsa_circ_97956,RMVar_hsa_circ_41340,RMVar_hsa_circ_113200,RMVar_hsa_circ_229824,RMVar_hsa_circ_229826,RMVar_hsa_circ_229828,RMVar_hsa_circ_229827,RMVar_hsa_circ_229825,RMVar_hsa_circ_83868,RMVar_hsa_circ_229832,RMVar_hsa_circ_229833,RMVar_hsa_circ_363695,RMVar_hsa_circ_368677,RMVar_hsa_circ_75936,RMVar_hsa_circ_51145,RMVar_hsa_circ_26323,RMVar_hsa_circ_34430,RMVar_hsa_circ_229834,RMVar_hsa_circ_229835,RMVar_hsa_circ_284015,RMVar_hsa_circ_291046 41889 RMVar_ID_41889 Human_SNP_ID_217251267 A-to-I Human chr4 + 185315420 185315420 185315420 GATTCAAGCAATTCTCCTCCCTCAGCCTCCCGAGTACCTGGAATTACAGGCGTGCACCACCACGC GATTCAAGCAATTCTCCTCCCTCAGCCTCCCGTGTACCTGGAATTACAGGCGTGCACCACCACGC A T SNX25 Ensembl:ENSG00000109762 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1167923211 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54915,RMVar_hsa_circ_117822,RMVar_hsa_circ_329071,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_229817,RMVar_hsa_circ_229816,RMVar_hsa_circ_229813,RMVar_hsa_circ_229814,RMVar_hsa_circ_229812,RMVar_hsa_circ_373593,RMVar_hsa_circ_98895,RMVar_hsa_circ_101722,RMVar_hsa_circ_97956,RMVar_hsa_circ_41340,RMVar_hsa_circ_113200,RMVar_hsa_circ_229824,RMVar_hsa_circ_229826,RMVar_hsa_circ_229828,RMVar_hsa_circ_229827,RMVar_hsa_circ_229825,RMVar_hsa_circ_83868,RMVar_hsa_circ_229832,RMVar_hsa_circ_229833,RMVar_hsa_circ_363695,RMVar_hsa_circ_368677,RMVar_hsa_circ_75936,RMVar_hsa_circ_51145,RMVar_hsa_circ_26323,RMVar_hsa_circ_34430,RMVar_hsa_circ_229834,RMVar_hsa_circ_229835,RMVar_hsa_circ_284015,RMVar_hsa_circ_291046 41890 RMVar_ID_41890 Human_SNP_ID_217251278 A-to-I Human chr4 + 185315459 185315459 185315459 GGAATTACAGGCGTGCACCACCACGCCCAGCTAATGTTTGTATTTTTAGTAGAGACAGGGCTTCA GGAATTACAGGCGTGCACCACCACGCCCAGCTGATGTTTGTATTTTTAGTAGAGACAGGGCTTCA A G SNX25 Ensembl:ENSG00000109762 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1484299567 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54915,RMVar_hsa_circ_117822,RMVar_hsa_circ_329071,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_229817,RMVar_hsa_circ_229816,RMVar_hsa_circ_229813,RMVar_hsa_circ_229814,RMVar_hsa_circ_229812,RMVar_hsa_circ_373593,RMVar_hsa_circ_98895,RMVar_hsa_circ_101722,RMVar_hsa_circ_97956,RMVar_hsa_circ_41340,RMVar_hsa_circ_113200,RMVar_hsa_circ_229824,RMVar_hsa_circ_229826,RMVar_hsa_circ_229828,RMVar_hsa_circ_229827,RMVar_hsa_circ_229825,RMVar_hsa_circ_83868,RMVar_hsa_circ_229832,RMVar_hsa_circ_229833,RMVar_hsa_circ_363695,RMVar_hsa_circ_368677,RMVar_hsa_circ_75936,RMVar_hsa_circ_51145,RMVar_hsa_circ_26323,RMVar_hsa_circ_34430,RMVar_hsa_circ_229834,RMVar_hsa_circ_229835,RMVar_hsa_circ_284015,RMVar_hsa_circ_291046 41891 RMVar_ID_41891 Human_SNP_ID_217251279 A-to-I Human chr4 + 185315459 185315459 185315459 GGAATTACAGGCGTGCACCACCACGCCCAGCTAATGTTTGTATTTTTAGTAGAGACAGGGCTTCA GGAATTACAGGCGTGCACCACCACGCCCAGCTTATGTTTGTATTTTTAGTAGAGACAGGGCTTCA A T SNX25 Ensembl:ENSG00000109762 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1484299567 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54915,RMVar_hsa_circ_117822,RMVar_hsa_circ_329071,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_229817,RMVar_hsa_circ_229816,RMVar_hsa_circ_229813,RMVar_hsa_circ_229814,RMVar_hsa_circ_229812,RMVar_hsa_circ_373593,RMVar_hsa_circ_98895,RMVar_hsa_circ_101722,RMVar_hsa_circ_97956,RMVar_hsa_circ_41340,RMVar_hsa_circ_113200,RMVar_hsa_circ_229824,RMVar_hsa_circ_229826,RMVar_hsa_circ_229828,RMVar_hsa_circ_229827,RMVar_hsa_circ_229825,RMVar_hsa_circ_83868,RMVar_hsa_circ_229832,RMVar_hsa_circ_229833,RMVar_hsa_circ_363695,RMVar_hsa_circ_368677,RMVar_hsa_circ_75936,RMVar_hsa_circ_51145,RMVar_hsa_circ_26323,RMVar_hsa_circ_34430,RMVar_hsa_circ_229834,RMVar_hsa_circ_229835,RMVar_hsa_circ_284015,RMVar_hsa_circ_291046 41892 RMVar_ID_41892 Human_SNP_ID_217251282 A-to-I Human chr4 + 185315483 185315483 185315483 GCCCAGCTAATGTTTGTATTTTTAGTAGAGACAGGGCTTCACCATGTTGGCCAGGCTGGTCTCAA GCCCAGCTAATGTTTGTATTTTTAGTAGAGACGGGGCTTCACCATGTTGGCCAGGCTGGTCTCAA A G SNX25 Ensembl:ENSG00000109762 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs932228401 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54915,RMVar_hsa_circ_117822,RMVar_hsa_circ_329071,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_229817,RMVar_hsa_circ_229816,RMVar_hsa_circ_229813,RMVar_hsa_circ_229814,RMVar_hsa_circ_229812,RMVar_hsa_circ_373593,RMVar_hsa_circ_98895,RMVar_hsa_circ_101722,RMVar_hsa_circ_97956,RMVar_hsa_circ_41340,RMVar_hsa_circ_113200,RMVar_hsa_circ_229824,RMVar_hsa_circ_229826,RMVar_hsa_circ_229828,RMVar_hsa_circ_229827,RMVar_hsa_circ_229825,RMVar_hsa_circ_83868,RMVar_hsa_circ_229832,RMVar_hsa_circ_229833,RMVar_hsa_circ_363695,RMVar_hsa_circ_368677,RMVar_hsa_circ_75936,RMVar_hsa_circ_51145,RMVar_hsa_circ_26323,RMVar_hsa_circ_34430,RMVar_hsa_circ_229834,RMVar_hsa_circ_229835,RMVar_hsa_circ_284015,RMVar_hsa_circ_291046 41893 RMVar_ID_41893 Human_SNP_ID_217251284 A-to-I Human chr4 + 185315494 185315494 185315494 GTTTGTATTTTTAGTAGAGACAGGGCTTCACCATGTTGGCCAGGCTGGTCTCAACCTGCTAAGTT GTTTGTATTTTTAGTAGAGACAGGGCTTCACCCTGTTGGCCAGGCTGGTCTCAACCTGCTAAGTT A C SNX25 Ensembl:ENSG00000109762 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs934731883 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54915,RMVar_hsa_circ_117822,RMVar_hsa_circ_329071,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_229817,RMVar_hsa_circ_229816,RMVar_hsa_circ_229813,RMVar_hsa_circ_229814,RMVar_hsa_circ_229812,RMVar_hsa_circ_373593,RMVar_hsa_circ_98895,RMVar_hsa_circ_101722,RMVar_hsa_circ_97956,RMVar_hsa_circ_41340,RMVar_hsa_circ_113200,RMVar_hsa_circ_229824,RMVar_hsa_circ_229826,RMVar_hsa_circ_229828,RMVar_hsa_circ_229827,RMVar_hsa_circ_229825,RMVar_hsa_circ_83868,RMVar_hsa_circ_229832,RMVar_hsa_circ_229833,RMVar_hsa_circ_363695,RMVar_hsa_circ_368677,RMVar_hsa_circ_75936,RMVar_hsa_circ_51145,RMVar_hsa_circ_26323,RMVar_hsa_circ_34430,RMVar_hsa_circ_229834,RMVar_hsa_circ_229835,RMVar_hsa_circ_284015,RMVar_hsa_circ_291046 41894 RMVar_ID_41894 Human_SNP_ID_217251300 A-to-I Human chr4 + 185315554 185315554 185315554 AAGTTCAGGTGATCCGCCTGCCTCTGTCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGTG AAGTTCAGGTGATCCGCCTGCCTCTGTCTCCCGAAGTGCTGGGATTACAGGCATGAGCCACTGTG A G SNX25 Ensembl:ENSG00000109762 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1003108741 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54915,RMVar_hsa_circ_117822,RMVar_hsa_circ_329071,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_229817,RMVar_hsa_circ_229816,RMVar_hsa_circ_229813,RMVar_hsa_circ_229814,RMVar_hsa_circ_229812,RMVar_hsa_circ_373593,RMVar_hsa_circ_98895,RMVar_hsa_circ_101722,RMVar_hsa_circ_97956,RMVar_hsa_circ_41340,RMVar_hsa_circ_113200,RMVar_hsa_circ_229824,RMVar_hsa_circ_229826,RMVar_hsa_circ_229828,RMVar_hsa_circ_229827,RMVar_hsa_circ_229825,RMVar_hsa_circ_83868,RMVar_hsa_circ_229832,RMVar_hsa_circ_229833,RMVar_hsa_circ_363695,RMVar_hsa_circ_368677,RMVar_hsa_circ_75936,RMVar_hsa_circ_51145,RMVar_hsa_circ_26323,RMVar_hsa_circ_34430,RMVar_hsa_circ_229834,RMVar_hsa_circ_229835,RMVar_hsa_circ_284015,RMVar_hsa_circ_291046 41895 RMVar_ID_41895 Human_SNP_ID_217252795 A-to-I Human chr4 + 185321437 185321437 185321437 GGTGTGTGCTACCACACCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTTACCGTGTTGG GGTGTGTGCTACCACACCCAGCTAATTTTTGTTTTTTTAGTAGAGACGGGGTTTTACCGTGTTGG A T SNX25 Ensembl:ENSG00000109762 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs146900257 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117822,RMVar_hsa_circ_329071,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_229817,RMVar_hsa_circ_229816,RMVar_hsa_circ_229813,RMVar_hsa_circ_229814,RMVar_hsa_circ_229812,RMVar_hsa_circ_373593,RMVar_hsa_circ_98895,RMVar_hsa_circ_97956,RMVar_hsa_circ_41340,RMVar_hsa_circ_113200,RMVar_hsa_circ_229824,RMVar_hsa_circ_229826,RMVar_hsa_circ_229827,RMVar_hsa_circ_229825,RMVar_hsa_circ_229833,RMVar_hsa_circ_363695,RMVar_hsa_circ_75936,RMVar_hsa_circ_51145,RMVar_hsa_circ_26323,RMVar_hsa_circ_34430,RMVar_hsa_circ_229834,RMVar_hsa_circ_229835,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 41896 RMVar_ID_41896 Human_SNP_ID_217252821 A-to-I Human chr4 + 185321543 185321543 185321543 CGTGGGCCTCCCAAAGTACTGGGATTACAGTCATGAGCCACCGCAGCCAGCTTTTATTTCAATTT CGTGGGCCTCCCAAAGTACTGGGATTACAGTCGTGAGCCACCGCAGCCAGCTTTTATTTCAATTT A G SNX25 Ensembl:ENSG00000109762 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1356425229 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117822,RMVar_hsa_circ_329071,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_229817,RMVar_hsa_circ_229816,RMVar_hsa_circ_229813,RMVar_hsa_circ_229814,RMVar_hsa_circ_229812,RMVar_hsa_circ_373593,RMVar_hsa_circ_98895,RMVar_hsa_circ_97956,RMVar_hsa_circ_41340,RMVar_hsa_circ_113200,RMVar_hsa_circ_229824,RMVar_hsa_circ_229826,RMVar_hsa_circ_229827,RMVar_hsa_circ_229825,RMVar_hsa_circ_229833,RMVar_hsa_circ_363695,RMVar_hsa_circ_75936,RMVar_hsa_circ_51145,RMVar_hsa_circ_26323,RMVar_hsa_circ_34430,RMVar_hsa_circ_229834,RMVar_hsa_circ_229835,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 41897 RMVar_ID_41897 Human_SNP_ID_217253019 A-to-I Human chr4 + 185322376 185322376 185322376 TTGCTTGAACCTGGGAAGGTGGAGGTTGCAGTAAGCCGAGATCACGCCACTACACTCCAGCCTGG TTGCTTGAACCTGGGAAGGTGGAGGTTGCAGTGAGCCGAGATCACGCCACTACACTCCAGCCTGG A G SNX25 Ensembl:ENSG00000109762 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs138578431 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117822,RMVar_hsa_circ_329071,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_229817,RMVar_hsa_circ_229816,RMVar_hsa_circ_229813,RMVar_hsa_circ_229814,RMVar_hsa_circ_229812,RMVar_hsa_circ_373593,RMVar_hsa_circ_98895,RMVar_hsa_circ_97956,RMVar_hsa_circ_41340,RMVar_hsa_circ_113200,RMVar_hsa_circ_229824,RMVar_hsa_circ_229826,RMVar_hsa_circ_229827,RMVar_hsa_circ_229825,RMVar_hsa_circ_229833,RMVar_hsa_circ_363695,RMVar_hsa_circ_75936,RMVar_hsa_circ_51145,RMVar_hsa_circ_26323,RMVar_hsa_circ_34430,RMVar_hsa_circ_229834,RMVar_hsa_circ_229835,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 41898 RMVar_ID_41898 Human_SNP_ID_217263542 A-to-I Human chr4 + 185366763 185366763 185366763 CAAAATTTAAACATTATTATTCAAAATTCACAAAACTAAGAGACAAATTTAAAGAATTAAACTTT CAAAATTTAAACATTATTATTCAAAATTCACAGAACTAAGAGACAAATTTAAAGAATTAAACTTT A G SNX25 Ensembl:ENSG00000109762 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1260645964 Functional Loss SNV dbSNP153 33..33 33 - - - 41899 RMVar_ID_41899 Human_SNP_ID_217263814 A-to-I Human chr4 + 185367911 185367911 185367911 TTAGAAAACTCTCCCTTATGGCCGGGCGCGGTAGCTCACACCTGTAATCCCAGCACTTTGGGAGG TTAGAAAACTCTCCCTTATGGCCGGGCGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGG A G SNX25 Ensembl:ENSG00000109762 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992632967 Functional Loss SNV dbSNP153 33..33 33 - - - 41900 RMVar_ID_41900 Human_SNP_ID_217264121 A-to-I Human chr4 + 185368996 185368996 185368996 TTGTATTTCTAGTAGAGATGGGATTTTGCCATATTGGACAGGTTGGTCTCACACTCTTGGCCTCA TTGTATTTCTAGTAGAGATGGGATTTTGCCATGTTGGACAGGTTGGTCTCACACTCTTGGCCTCA A G SNX25 Ensembl:ENSG00000109762 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs551191560 Functional Loss SNV dbSNP153 33..33 33 - - - 41901 RMVar_ID_41901 Human_SNP_ID_217264248 A-to-I Human chr4 + 185369444 185369444 185369444 TTTAGTATTTTTAGTAGAGACCCAGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCT TTTAGTATTTTTAGTAGAGACCCAGTTTCACCGTGTTGGCCAGGCTGGTCTCGAACTCCTGACCT A G SNX25 Ensembl:ENSG00000109762 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1235313361 Functional Loss SNV dbSNP153 33..33 33 - - - 41902 RMVar_ID_41902 Human_SNP_ID_217265816 A-to-I Human chr4 + 185375137 185375136 185375138 CAAATATATTTTGGTTTTTGTTTGTTTGAGACAGAGTCTTGCTCTGTCACCCAGGCTGGAGTGCA CAAATATATTTTGGTTTTTGTTTGTTTGAGAC__AGTCTTGCTCTGTCACCCAGGCTGGAGTGCA CAG C AC112722.1 Ensembl:ENSG00000250410 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1180675912 Functional Loss DEL dbSNP153 33..34 33 - - - 41903 RMVar_ID_41903 Human_SNP_ID_217266644 A-to-I Human chr4 - 185377308 185377308 185377308 CTCCATGTTGGTCAGGCTAGTCTTGAACTCCCAAACTCAGGTGATCCACCCGCCTCGGCCTCCCA CTCCATGTTGGTCAGGCTAGTCTTGAACTCCCCAACTCAGGTGATCCACCCGCCTCGGCCTCCCA T G LRP2BP Ensembl:ENSG00000109771 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1391802184 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67640 41904 RMVar_ID_41904 Human_SNP_ID_217280653 A-to-I Human chr4 + 185429744 185429744 185429744 AGGCTGGAGTGCCAGTGGCCTGATTATAGCTCACTGCAGTCTCAAACTCCTGGGCTCAAGGGTTC AGGCTGGAGTGCCAGTGGCCTGATTATAGCTCGCTGCAGTCTCAAACTCCTGGGCTCAAGGGTTC A G C4orf47 Ensembl:ENSG00000205129 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs560542192 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_292348,RMVar_hsa_circ_229856 41905 RMVar_ID_41905 Human_SNP_ID_217281398 A-to-I Human chr4 + 185432812 185432812 185432812 TTGAGCCCAGGAGTTTGAGGTTACAGTGAGCTATGATTGAGCCACTGCACTCCAGCCTGGATGTC TTGAGCCCAGGAGTTTGAGGTTACAGTGAGCTGTGATTGAGCCACTGCACTCCAGCCTGGATGTC A G C4orf47 Ensembl:ENSG00000205129 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1255198695 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_292348,RMVar_hsa_circ_229856 41906 RMVar_ID_41906 Human_SNP_ID_217365855 A-to-I Human chr4 - 185768474 185768474 185768474 GCTGCCAGGCTGGTCTCATAGTCCAGACCTCAAGTGATCCACCCACCTCGGCCTTCCAAGATGCT GCTGCCAGGCTGGTCTCATAGTCCAGACCTCAGGTGATCCACCCACCTCGGCCTTCCAAGATGCT T C SORBS2 Ensembl:ENSG00000154556 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1242763088 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_324587,RMVar_hsa_circ_365326,RMVar_hsa_circ_358337 41907 RMVar_ID_41907 Human_SNP_ID_217585105 A-to-I Human chr4 - 186603797 186603797 186603797 AGATCCATGCCACAGACCAGGACGTGTATGATACTCTAACCTACAGTCTCGACCCTCAGATGGAC AGATCCATGCCACAGACCAGGACGTGTATGATGCTCTAACCTACAGTCTCGACCCTCAGATGGAC T C FAT1 Ensembl:ENSG00000083857 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs772909331 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8878597,Human_RBP_ID_17294357,Human_RBP_ID_17523542,Human_RBP_ID_18023588,Human_RBP_ID_22400568 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_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 41908 RMVar_ID_41908 Human_SNP_ID_217930558 A-to-I Human chr4 - 187953323 187953323 187953323 GGAGGCCGAGGCAGGCAGATCACTTGAGGTCAAGAGTTCGAGACCAGCCTGGCCGGCGTGGCGAA GGAGGCCGAGGCAGGCAGATCACTTGAGGTCAGGAGTTCGAGACCAGCCTGGCCGGCGTGGCGAA T C AC108073.3 Ensembl:ENSG00000286641 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1560898441 Functional Loss SNV dbSNP153 33..33 33 - - - 41909 RMVar_ID_41909 Human_SNP_ID_217944619 A-to-I Human chr4 + 188004218 188004218 188004218 GCCTGTAATCCCAACACTTTGTTGGGAGGCCAAAGCAGGAGGATAGCTTGAGGCCAGGAGTTCCA GCCTGTAATCCCAACACTTTGTTGGGAGGCCAGAGCAGGAGGATAGCTTGAGGCCAGGAGTTCCA A G ZFP42 Ensembl:ENSG00000179059 Protein coding 3'UTR GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1287536420 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101144,RMVar_hsa_circ_229921 41910 RMVar_ID_41910 Human_SNP_ID_217944763 A-to-I Human chr4 + 188004690 188004690 188004690 TACGCCTGTGTTCCCAGCTACTCAGGAGGCTGAAGCAGGAGGATAGCTTGAGCCCAGGAGTTTGA TACGCCTGTGTTCCCAGCTACTCAGGAGGCTGGAGCAGGAGGATAGCTTGAGCCCAGGAGTTTGA A G ZFP42 Ensembl:ENSG00000179059 Protein coding 3'UTR GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1041129500 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101144,RMVar_hsa_circ_229921 41911 RMVar_ID_41911 Human_SNP_ID_217971570 A-to-I Human chr4 - 188097930 188097930 188097930 TTTAGTAGAAACGGGGTTTCACCATGTTGGTCAGTCTGGTCTTAAACTCCCGACCTCAGGTTATA TTTAGTAGAAACGGGGTTTCACCATGTTGGTCTGTCTGGTCTTAAACTCCCGACCTCAGGTTATA T A TRIML2 Ensembl:ENSG00000179046 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1243497144 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15114618 RMVar_hsa_circ_346083 41912 RMVar_ID_41912 Human_SNP_ID_218486673 A-to-I Human chr4 + 189940968 189940968 189940968 CCCCTGTGCTGCCCCGACTCACATACTCGTCCAGAACCGGCCTCAGCCTCTCCGCGCAGAAGTTT CCCCTGTGCTGCCCCGACTCACATACTCGTCCCGAACCGGCCTCAGCCTCTCCGCGCAGAAGTTT A C FRG1 Ensembl:ENSG00000109536 Protein coding 5'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1339357786 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4780819,Human_RBP_ID_8882209,Human_RBP_ID_9334839,Human_RBP_ID_26349676 41913 RMVar_ID_41913 Human_SNP_ID_218486674 A-to-I Human chr4 + 189940968 189940968 189940968 CCCCTGTGCTGCCCCGACTCACATACTCGTCCAGAACCGGCCTCAGCCTCTCCGCGCAGAAGTTT CCCCTGTGCTGCCCCGACTCACATACTCGTCCTGAACCGGCCTCAGCCTCTCCGCGCAGAAGTTT A T FRG1 Ensembl:ENSG00000109536 Protein coding 5'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1339357786 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4780819,Human_RBP_ID_8882209,Human_RBP_ID_9334839,Human_RBP_ID_26349676 41914 RMVar_ID_41914 Human_SNP_ID_218487494 A-to-I Human chr4 - 189943223 189943218 189943223 GTTTCTTCATCTTCTTCTCTTTTTCTTTTCTTATCTTTGCTCTTTTTCTTCTTACTACAGGACAT GTTTCTTCATCTTCTTCTCTTTTTCTTTTCTT_____TGCTCTTTTTCTTCTTACTACAGGACAT AAAGAT A - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1468463162 Functional Loss DEL dbSNP153 33..37 33 - - - 41915 RMVar_ID_41915 Human_SNP_ID_218487497 A-to-I Human chr4 - 189943223 189943223 189943223 GTTTCTTCATCTTCTTCTCTTTTTCTTTTCTTATCTTTGCTCTTTTTCTTCTTACTACAGGACAT GTTTCTTCATCTTCTTCTCTTTTTCTTTTCTTCTCTTTGCTCTTTTTCTTCTTACTACAGGACAT T G - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs373444578 Functional Loss SNV dbSNP153 33..33 33 - - - 41916 RMVar_ID_41916 Human_SNP_ID_218492227 A-to-I Human chr4 - 189957414 189957414 189957414 CATTGCATCTAATAAAGCAGCTATTTGAGGCCAACAAAGCCATTTTCCCCTAAGTGAAACAAATA CATTGCATCTAATAAAGCAGCTATTTGAGGCCTACAAAGCCATTTTCCCCTAAGTGAAACAAATA T A lnc-FRG2-11 RNACentral:URS00008BB8A8 lincRNA intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs575384276 Functional Loss SNV dbSNP153 33..33 33 - - - 41917 RMVar_ID_41917 Human_SNP_ID_218492228 A-to-I Human chr4 - 189957414 189957414 189957414 CATTGCATCTAATAAAGCAGCTATTTGAGGCCAACAAAGCCATTTTCCCCTAAGTGAAACAAATA CATTGCATCTAATAAAGCAGCTATTTGAGGCCGACAAAGCCATTTTCCCCTAAGTGAAACAAATA T C lnc-FRG2-11 RNACentral:URS00008BB8A8 lincRNA intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs575384276 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 41918 RMVar_ID_41918 Human_SNP_ID_218493399 A-to-I Human chr4 + 189960945 189960945 189960945 ACCTACTTAGCTGGGCATGGTGGTACATGCCTATAGGCCCAGCTACTCGGGAGGCTGAGACAGGA ACCTACTTAGCTGGGCATGGTGGTACATGCCTGTAGGCCCAGCTACTCGGGAGGCTGAGACAGGA A G FRG1 Ensembl:ENSG00000109536 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11132779 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_630560 RMVar_hsa_circ_268043,RMVar_hsa_circ_64893 41919 RMVar_ID_41919 Human_SNP_ID_218493416 A-to-I Human chr4 + 189961023 189961021 189961024 CCAGGAGTTCAAGGCTGCAGTGAGCTCTGATCACCACTGCCTTCCAGCCTGGGTGGCAGAGCAAG CCAGGAGTTCAAGGCTGCAGTGAGCTCTGAT___CACTGCCTTCCAGCCTGGGTGGCAGAGCAAG TCAC T FRG1 Ensembl:ENSG00000109536 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1469860172 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_268043,RMVar_hsa_circ_64893 41920 RMVar_ID_41920 Human_SNP_ID_486449686 A-to-I Human chr11 - 130000226 130000226 130000226 TAGCCTGGCCAACATGGTGAAAGCCTGTCTCTACTAAAAATACAAAAATTGGACGGACATGATGG TAGCCTGGCCAACATGGTGAAAGCCTGTCTCTTCTAAAAATACAAAAATTGGACGGACATGATGG T A PRDM10 Ensembl:ENSG00000170325 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1565521058 Functional Loss SNV dbSNP153 33..33 33 - - - 41921 RMVar_ID_41921 Human_SNP_ID_486449923 A-to-I Human chr11 - 130001076 130001076 130001076 TTTAGGAGACAGGGTCTCTGGTTGCCCAGGCTAGAGTGCAGTGGCGCGATCTTGGCTCACTGCCG TTTAGGAGACAGGGTCTCTGGTTGCCCAGGCTGGAGTGCAGTGGCGCGATCTTGGCTCACTGCCG T C PRDM10 Ensembl:ENSG00000170325 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1233330450 Functional Loss SNV dbSNP153 33..33 33 - - - 41922 RMVar_ID_41922 Human_SNP_ID_486449927 A-to-I Human chr11 - 130001098 130001098 130001098 GAAAGGAACTTTGCTAGGTTTATTTAGGAGACAGGGTCTCTGGTTGCCCAGGCTAGAGTGCAGTG GAAAGGAACTTTGCTAGGTTTATTTAGGAGACGGGGTCTCTGGTTGCCCAGGCTAGAGTGCAGTG T C PRDM10 Ensembl:ENSG00000170325 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1329683650 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11561390 41923 RMVar_ID_41923 Human_SNP_ID_486521707 A-to-I Human chr11 - 130267164 130267164 130267164 TGCTTCCCAAGCTCATGCAGTCCTCCAGTCTCAGCCTCCTGAGTAGCTGGGACTACAGGCATGTG TGCTTCCCAAGCTCATGCAGTCCTCCAGTCTCGGCCTCCTGAGTAGCTGGGACTACAGGCATGTG T C ZBTB44 Ensembl:ENSG00000196323 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1361326716 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86537,RMVar_hsa_circ_154057 41924 RMVar_ID_41924 Human_SNP_ID_486530055 A-to-I Human chr11 - 130298259 130298259 130298259 GCATGCCTGTAGTCCCAGCTATTCAGGAAGCTAAGGTGGGAGGATTGCTTGAGTTCGGGAGGTCC GCATGCCTGTAGTCCCAGCTATTCAGGAAGCTGAGGTGGGAGGATTGCTTGAGTTCGGGAGGTCC T C ZBTB44 Ensembl:ENSG00000196323 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903014607 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86537,RMVar_hsa_circ_154057 41925 RMVar_ID_41925 Human_SNP_ID_486534069 A-to-I Human chr11 - 130313641 130313641 130313641 GTAAGTAGATAATCTCTTGAAGTCAGGAAGAAATTCTCCATAACTTCCACTTATTTTCTTAATGC GTAAGTAGATAATCTCTTGAAGTCAGGAAGAATTTCTCCATAACTTCCACTTATTTTCTTAATGC T A ZBTB44 Ensembl:ENSG00000196323 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1300668676 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17792385,Human_RBP_ID_18604959 RMVar_hsa_circ_86537,RMVar_hsa_circ_154057 41926 RMVar_ID_41926 Human_SNP_ID_486571541 A-to-I Human chr11 + 130459126 130459126 130459126 CGTGATCACGGGTCACTGTAGATTACCCTCCCAGGCTCAAGTGATCCTCCTACCTCAGCCTCCTC CGTGATCACGGGTCACTGTAGATTACCCTCCCGGGCTCAAGTGATCCTCCTACCTCAGCCTCCTC A G ADAMTS15 Ensembl:ENSG00000166106 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs951459862 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_154063,RMVar_hsa_circ_97990 41927 RMVar_ID_41927 Human_SNP_ID_486672762 A-to-I Human chr11 - 130870656 130870654 130870656 TCCTTTCTCCCAACCTTCCACATCCCAGAGACAGGGTGCTGGTGACTTTTATGGAAAGGCTTGAA TCCTTTCTCCCAACCTTCCACATCCCAGAGAC__GGTGCTGGTGACTTTTATGGAAAGGCTTGAA CCT C LINC02551 RNACentral:URS00008C030C lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1241279223 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_19611780 41928 RMVar_ID_41928 Human_SNP_ID_486884378 A-to-I Human chr11 - 131663493 131663491 131663493 TCAGTGGCCTGGCCCGTGCTGCAGACAGACAGAGCGGTCAAGGAAGGCCTCAGGACCAGAGGCAG TCAGTGGCCTGGCCCGTGCTGCAGACAGACAG__CGGTCAAGGAAGGCCTCAGGACCAGAGGCAG GCT G NTM-AS1 Ensembl:ENSG00000224795 lincRNA exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1332602505 Functional Loss DEL dbSNP153 33..34 33 - - - 41929 RMVar_ID_41929 Human_SNP_ID_486884380 A-to-I Human chr11 - 131663493 131663493 131663493 TCAGTGGCCTGGCCCGTGCTGCAGACAGACAGAGCGGTCAAGGAAGGCCTCAGGACCAGAGGCAG TCAGTGGCCTGGCCCGTGCTGCAGACAGACAGGGCGGTCAAGGAAGGCCTCAGGACCAGAGGCAG T C NTM-AS1 Ensembl:ENSG00000224795 lincRNA exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1004906139 Functional Loss SNV dbSNP153 33..33 33 - - - 41930 RMVar_ID_41930 Human_SNP_ID_486957594 A-to-I Human chr11 + 131931378 131931378 131931378 GGAAGATTGCTTGAGCCCAGGAGGTCGAGGCTACAGTGAACCGAGATGGCGCCACTGCAGTCCAG GGAAGATTGCTTGAGCCCAGGAGGTCGAGGCTGCAGTGAACCGAGATGGCGCCACTGCAGTCCAG A G NTM Ensembl:ENSG00000182667 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1487101636 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15039,RMVar_hsa_circ_49253 41931 RMVar_ID_41931 Human_SNP_ID_487024981 A-to-I Human chr11 + 132183596 132183596 132183596 TCCCAGCAAGGTATTCTAAAACAGAAATCGCTACTCCCTTTGACAACACAAGTGTCATCTGAAAA TCCCAGCAAGGTATTCTAAAACAGAAATCGCTGCTCCCTTTGACAACACAAGTGTCATCTGAAAA A G NTM Ensembl:ENSG00000182667 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1301704444 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15039,RMVar_hsa_circ_49253,RMVar_hsa_circ_333849,RMVar_hsa_circ_38018,RMVar_hsa_circ_154081 41932 RMVar_ID_41932 Human_SNP_ID_487116550 A-to-I Human chr11 - 132518389 132518389 132518389 CTACAGCCCTTTAAAGAGTTAGGTCCTTTGCAAGGACATGGATGAAGCTGGAAGCCATCATCCTC CTACAGCCCTTTAAAGAGTTAGGTCCTTTGCAGGGACATGGATGAAGCTGGAAGCCATCATCCTC T C OPCML Ensembl:ENSG00000183715 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1257615682 Functional Loss SNV dbSNP153 33..33 33 - - - 41933 RMVar_ID_41933 Human_SNP_ID_487150533 A-to-I Human chr11 - 132649226 132649226 132649226 CTTGTATCAGGCCTTTTCTCCCACTGTTGTGAAGATACATGTGGGGCTTTGTTCTGCTTTGCTTT CTTGTATCAGGCCTTTTCTCCCACTGTTGTGACGATACATGTGGGGCTTTGTTCTGCTTTGCTTT T G OPCML Ensembl:ENSG00000183715 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1292652755 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_332813 41934 RMVar_ID_41934 Human_SNP_ID_487216211 A-to-I Human chr11 - 132907487 132907487 132907487 AGCTGAGAATACAAGGGTGTGCCACCATGCCCAGCTAATTTTTATATTTTTAGTAGAGATGGGGT AGCTGAGAATACAAGGGTGTGCCACCATGCCCGGCTAATTTTTATATTTTTAGTAGAGATGGGGT T C OPCML Ensembl:ENSG00000183715 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1442370634 Functional Loss SNV dbSNP153 33..33 33 - - - 41935 RMVar_ID_41935 Human_SNP_ID_487220615 A-to-I Human chr11 - 132925249 132925249 132925249 AAACATCAGCATAAGACTCAGATATGGCAGGGATGTTTGAGCTATCACACTGGCAGTTTGAAATT AAACATCAGCATAAGACTCAGATATGGCAGGGGTGTTTGAGCTATCACACTGGCAGTTTGAAATT T C OPCML Ensembl:ENSG00000183715 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs921273303 Functional Loss SNV dbSNP153 33..33 33 - - - 41936 RMVar_ID_41936 Human_SNP_ID_487572624 A-to-I Human chr11 + 134226307 134226307 134226307 GCTTGCCGGTAGTCCTAGCTCCTCGGGGGGCTAAGATGGGAGGATTGTTTGAACCCAGGAGTTCC GCTTGCCGGTAGTCCTAGCTCCTCGGGGGGCTCAGATGGGAGGATTGTTTGAACCCAGGAGTTCC A C VPS26B Ensembl:ENSG00000151502 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1160351921 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114768,RMVar_hsa_circ_154117 41937 RMVar_ID_41937 Human_SNP_ID_487615149 A-to-I Human chr11 - 134379811 134379792 134379811 AGACCTCAGGGTGGAGTGAGCCCATGGTGGGCAGTGGGCAAGGCGGTGGGTGGTGGGCAAGGTGG AGACCTCAGGGTGGAGTGAGCCCATGGTGGGC___________________GGTGGGCAAGGTGG CACCCACCGCCTTGCCCACT C B3GAT1 Ensembl:ENSG00000109956 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1487646238 Functional Loss DEL dbSNP153 33..51 33 - - - RMVar_hsa_circ_127943,RMVar_hsa_circ_154134 41938 RMVar_ID_41938 Human_SNP_ID_487615156 A-to-I Human chr11 - 134379811 134379811 134379811 AGACCTCAGGGTGGAGTGAGCCCATGGTGGGCAGTGGGCAAGGCGGTGGGTGGTGGGCAAGGTGG AGACCTCAGGGTGGAGTGAGCCCATGGTGGGCGGTGGGCAAGGCGGTGGGTGGTGGGCAAGGTGG T C B3GAT1 Ensembl:ENSG00000109956 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903559680 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127943,RMVar_hsa_circ_154134 41939 RMVar_ID_41939 Human_SNP_ID_536550168 A-to-I Human chr13 - 75334686 75334686 75334686 CCAGCTACTCAGGAGGCTGAGGCACGAGAATCACTGGAACCCAGCAGGCAGGGGTTGCAGTGAGC CCAGCTACTCAGGAGGCTGAGGCACGAGAATCCCTGGAACCCAGCAGGCAGGGGTTGCAGTGAGC T G TBC1D4 Ensembl:ENSG00000136111 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1209278246 Functional Loss SNV dbSNP153 33..33 33 - - - 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 41940 RMVar_ID_41940 Human_SNP_ID_536595522 A-to-I Human chr13 - 75526632 75526632 75526632 TATTATTTTCCCCCTTTCTCTCCAGAATTTCTACAGACAGTTCAAGGAAATTGCTGCAGTTATTG TATTATTTTCCCCCTTTCTCTCCAGAATTTCTGCAGACAGTTCAAGGAAATTGCTGCAGTTATTG T C COMMD6 Ensembl:ENSG00000188243 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1270872352 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4273833,Human_RBP_ID_9036384,Human_RBP_ID_23208383 Human_Splice_Rec_1471734,Human_Splice_Rec_1471742,Human_Splice_Rec_1471744,Human_Splice_Rec_1471748,Human_Splice_Rec_1471754,Human_Splice_Rec_1471760,Human_Splice_Rec_1471768,Human_Splice_Rec_1471774,Human_Splice_Rec_1471778 41941 RMVar_ID_41941 Human_SNP_ID_536597326 A-to-I Human chr13 - 75533474 75533474 75533474 TCCTTGACCTCCTGGGCTTAGGTGATCCTCCCACTTCATCCTCCCAAGTAGCTGGGACTTAAAGG TCCTTGACCTCCTGGGCTTAGGTGATCCTCCCGCTTCATCCTCCCAAGTAGCTGGGACTTAAAGG T C COMMD6 Ensembl:ENSG00000188243 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1318594813 Functional Loss SNV dbSNP153 33..33 33 - - - 41942 RMVar_ID_41942 Human_SNP_ID_536633767 A-to-I Human chr13 + 75686412 75686412 75686412 AACAGCATGGGAAAGACTTCCCCACATGATTCAATTATCTCCCACCTGGTCCCTCCCACAACACA AACAGCATGGGAAAGACTTCCCCACATGATTCGATTATCTCCCACCTGGTCCCTCCCACAACACA A G AL137782.1,LMO7 Ensembl:ENSG00000261553,Ensembl:ENSG00000136153 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1045149885 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_89506,RMVar_hsa_circ_126931,RMVar_hsa_circ_163784,RMVar_hsa_circ_163785 41943 RMVar_ID_41943 Human_SNP_ID_536964000 A-to-I Human chr13 + 76987625 76987625 76987625 CCCTTTTATCAGTATTCCAAGCCGGAGATGATACTAGAATGGGTGGAGAAGAAGCAGAAATACGT CCCTTTTATCAGTATTCCAAGCCGGAGATGATGCTAGAATGGGTGGAGAAGAAGCAGAAATACGT A G DHX9P1 Ensembl:ENSG00000228002 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879077214 Functional Loss SNV dbSNP153 33..33 33 - - - 41944 RMVar_ID_41944 Human_SNP_ID_536964162 A-to-I Human chr13 - 76988304 76988304 76988304 CATCTTAGGAGGACCTGGACCATCTCCATACCATGTACTGCCAATCATAAGGTTGATATCAGCAG CATCTTAGGAGGACCTGGACCATCTCCATACCGTGTACTGCCAATCATAAGGTTGATATCAGCAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1454213216 Functional Loss SNV dbSNP153 33..33 33 - - - 41945 RMVar_ID_41945 Human_SNP_ID_536964169 A-to-I Human chr13 - 76988330 76988330 76988330 TATCCGCTTCCATTGTCATATTGGGCCATCTTAGGAGGACCTGGACCATCTCCATACCATGTACT TATCCGCTTCCATTGTCATATTGGGCCATCTTGGGAGGACCTGGACCATCTCCATACCATGTACT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1400508076 Functional Loss SNV dbSNP153 33..33 33 - - - 41946 RMVar_ID_41946 Human_SNP_ID_536970150 A-to-I Human chr13 - 77011641 77011641 77011641 CTGGCTTACTGCAGTCTGGACCTCCTGGGCTTAAACGATCTTCTCACCTCAGCCTCCCAAGTAGC CTGGCTTACTGCAGTCTGGACCTCCTGGGCTTTAACGATCTTCTCACCTCAGCCTCCCAAGTAGC T A FBXL3 Ensembl:ENSG00000005812 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1197808438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9743983,Human_RBP_ID_12219905 41947 RMVar_ID_41947 Human_SNP_ID_537004194 A-to-I Human chr13 - 77157362 77157362 77157362 AAAATTAGCCAGGCATGGTGGCACACTCCTGTAGTCCCAGCTACTTGGAGGCTGAGGTGGAAGGA AAAATTAGCCAGGCATGGTGGCACACTCCTGTGGTCCCAGCTACTTGGAGGCTGAGGTGGAAGGA T C MYCBP2 Ensembl:ENSG00000005810 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1300930358 Functional Loss SNV dbSNP153 33..33 33 - - - 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_111742,RMVar_hsa_circ_163829,RMVar_hsa_circ_124062,RMVar_hsa_circ_163841,RMVar_hsa_circ_7226,RMVar_hsa_circ_109703,RMVar_hsa_circ_100074,RMVar_hsa_circ_163844,RMVar_hsa_circ_163845,RMVar_hsa_circ_354598,RMVar_hsa_circ_100693,RMVar_hsa_circ_163851,RMVar_hsa_circ_24266,RMVar_hsa_circ_94635,RMVar_hsa_circ_113731,RMVar_hsa_circ_120994,RMVar_hsa_circ_163855,RMVar_hsa_circ_344344,RMVar_hsa_circ_119808,RMVar_hsa_circ_103401,RMVar_hsa_circ_110426,RMVar_hsa_circ_103365,RMVar_hsa_circ_42233,RMVar_hsa_circ_78772,RMVar_hsa_circ_92922,RMVar_hsa_circ_47374,RMVar_hsa_circ_30165,RMVar_hsa_circ_11126,RMVar_hsa_circ_14437,RMVar_hsa_circ_163857,RMVar_hsa_circ_163861,RMVar_hsa_circ_163863,RMVar_hsa_circ_163864,RMVar_hsa_circ_163862,RMVar_hsa_circ_163859,RMVar_hsa_circ_163860,RMVar_hsa_circ_163858,RMVar_hsa_circ_43506,RMVar_hsa_circ_105268,RMVar_hsa_circ_163868,RMVar_hsa_circ_315395,RMVar_hsa_circ_82867,RMVar_hsa_circ_45674,RMVar_hsa_circ_24468,RMVar_hsa_circ_100744,RMVar_hsa_circ_163870,RMVar_hsa_circ_163871,RMVar_hsa_circ_349759,RMVar_hsa_circ_49272,RMVar_hsa_circ_34909,RMVar_hsa_circ_163873,RMVar_hsa_circ_8683,RMVar_hsa_circ_118177,RMVar_hsa_circ_163875 41948 RMVar_ID_41948 Human_SNP_ID_537011492 A-to-I Human chr13 - 77186950 77186950 77186950 AAAATTAGCTGGGTATGGTGGTGCGCACTTGTAGTCCCAGCTGCTTGGGAGGCTGAGGGGGTGGT AAAATTAGCTGGGTATGGTGGTGCGCACTTGTCGTCCCAGCTGCTTGGGAGGCTGAGGGGGTGGT T G MYCBP2 Ensembl:ENSG00000005810 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs985042812 Functional Loss SNV dbSNP153 33..33 33 - - - 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_111742,RMVar_hsa_circ_163829,RMVar_hsa_circ_124062,RMVar_hsa_circ_163841,RMVar_hsa_circ_109703,RMVar_hsa_circ_163845,RMVar_hsa_circ_354598,RMVar_hsa_circ_100693,RMVar_hsa_circ_163851,RMVar_hsa_circ_94635,RMVar_hsa_circ_113731,RMVar_hsa_circ_120994,RMVar_hsa_circ_163855,RMVar_hsa_circ_103365,RMVar_hsa_circ_42233,RMVar_hsa_circ_78772,RMVar_hsa_circ_92922,RMVar_hsa_circ_47374,RMVar_hsa_circ_30165,RMVar_hsa_circ_11126,RMVar_hsa_circ_163857,RMVar_hsa_circ_163861,RMVar_hsa_circ_163859,RMVar_hsa_circ_163860,RMVar_hsa_circ_163858,RMVar_hsa_circ_82867,RMVar_hsa_circ_100744,RMVar_hsa_circ_163871,RMVar_hsa_circ_49272,RMVar_hsa_circ_163873,RMVar_hsa_circ_118177,RMVar_hsa_circ_25167,RMVar_hsa_circ_163875,RMVar_hsa_circ_29960,RMVar_hsa_circ_89696,RMVar_hsa_circ_163880,RMVar_hsa_circ_9375,RMVar_hsa_circ_32270,RMVar_hsa_circ_163883,RMVar_hsa_circ_53233,RMVar_hsa_circ_75091,RMVar_hsa_circ_163885,RMVar_hsa_circ_17100,RMVar_hsa_circ_108512,RMVar_hsa_circ_40550,RMVar_hsa_circ_98933,RMVar_hsa_circ_93400,RMVar_hsa_circ_19440,RMVar_hsa_circ_163889,RMVar_hsa_circ_266522,RMVar_hsa_circ_163890,RMVar_hsa_circ_163892,RMVar_hsa_circ_76077,RMVar_hsa_circ_163891 41949 RMVar_ID_41949 Human_SNP_ID_537027983 A-to-I Human chr13 - 77254836 77254836 77254836 AAACCAGGGACAGAGACAAATATCACTCATATATGGGAACTAAAAAATTGATTTCATGGAGATAG AAACCAGGGACAGAGACAAATATCACTCATATGTGGGAACTAAAAAATTGATTTCATGGAGATAG T C MYCBP2 Ensembl:ENSG00000005810 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs573908758 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79007,RMVar_hsa_circ_122811,RMVar_hsa_circ_163820,RMVar_hsa_circ_163821,RMVar_hsa_circ_3612,RMVar_hsa_circ_109703,RMVar_hsa_circ_163845,RMVar_hsa_circ_100693,RMVar_hsa_circ_163851,RMVar_hsa_circ_113731,RMVar_hsa_circ_103365,RMVar_hsa_circ_92922,RMVar_hsa_circ_163857,RMVar_hsa_circ_163859,RMVar_hsa_circ_163858,RMVar_hsa_circ_82867,RMVar_hsa_circ_163871,RMVar_hsa_circ_3929,RMVar_hsa_circ_98933,RMVar_hsa_circ_163889,RMVar_hsa_circ_34792,RMVar_hsa_circ_319130,RMVar_hsa_circ_45187,RMVar_hsa_circ_163897,RMVar_hsa_circ_110510,RMVar_hsa_circ_325966,RMVar_hsa_circ_268533,RMVar_hsa_circ_9368,RMVar_hsa_circ_163908,RMVar_hsa_circ_334568,RMVar_hsa_circ_372437,RMVar_hsa_circ_54481,RMVar_hsa_circ_163909,RMVar_hsa_circ_163910,RMVar_hsa_circ_102095,RMVar_hsa_circ_106883,RMVar_hsa_circ_106679,RMVar_hsa_circ_163916,RMVar_hsa_circ_163917,RMVar_hsa_circ_163915,RMVar_hsa_circ_271716,RMVar_hsa_circ_280227,RMVar_hsa_circ_319100,RMVar_hsa_circ_72890,RMVar_hsa_circ_163920,RMVar_hsa_circ_163922,RMVar_hsa_circ_54122,RMVar_hsa_circ_163921,RMVar_hsa_circ_163923,RMVar_hsa_circ_38542,RMVar_hsa_circ_323919,RMVar_hsa_circ_341923,RMVar_hsa_circ_55439,RMVar_hsa_circ_163924 41950 RMVar_ID_41950 Human_SNP_ID_537028022 A-to-I Human chr13 - 77255024 77255024 77255024 GTTTATCATAGCCATATCCACAACACCAAGATATGGAATCAACTTAAGTATCCATCAACAGATGA GTTTATCATAGCCATATCCACAACACCAAGATGTGGAATCAACTTAAGTATCCATCAACAGATGA T C MYCBP2 Ensembl:ENSG00000005810 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1345049411 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79007,RMVar_hsa_circ_122811,RMVar_hsa_circ_163820,RMVar_hsa_circ_163821,RMVar_hsa_circ_3612,RMVar_hsa_circ_109703,RMVar_hsa_circ_163845,RMVar_hsa_circ_100693,RMVar_hsa_circ_163851,RMVar_hsa_circ_113731,RMVar_hsa_circ_103365,RMVar_hsa_circ_92922,RMVar_hsa_circ_163857,RMVar_hsa_circ_163859,RMVar_hsa_circ_163858,RMVar_hsa_circ_82867,RMVar_hsa_circ_163871,RMVar_hsa_circ_3929,RMVar_hsa_circ_98933,RMVar_hsa_circ_163889,RMVar_hsa_circ_34792,RMVar_hsa_circ_319130,RMVar_hsa_circ_45187,RMVar_hsa_circ_163897,RMVar_hsa_circ_110510,RMVar_hsa_circ_325966,RMVar_hsa_circ_268533,RMVar_hsa_circ_9368,RMVar_hsa_circ_163908,RMVar_hsa_circ_334568,RMVar_hsa_circ_372437,RMVar_hsa_circ_54481,RMVar_hsa_circ_163909,RMVar_hsa_circ_163910,RMVar_hsa_circ_102095,RMVar_hsa_circ_106883,RMVar_hsa_circ_106679,RMVar_hsa_circ_163916,RMVar_hsa_circ_163917,RMVar_hsa_circ_163915,RMVar_hsa_circ_271716,RMVar_hsa_circ_280227,RMVar_hsa_circ_319100,RMVar_hsa_circ_72890,RMVar_hsa_circ_163920,RMVar_hsa_circ_163922,RMVar_hsa_circ_54122,RMVar_hsa_circ_163921,RMVar_hsa_circ_163923,RMVar_hsa_circ_38542,RMVar_hsa_circ_323919,RMVar_hsa_circ_341923,RMVar_hsa_circ_55439,RMVar_hsa_circ_163924 41951 RMVar_ID_41951 Human_SNP_ID_537028038 A-to-I Human chr13 - 77255083 77255083 77255083 GGGTATATGTATCAAAAAGAAAGGAAATCTGTATGTCAGAGAGATGCCTGCATTCTCAGGTTTAT GGGTATATGTATCAAAAAGAAAGGAAATCTGTTTGTCAGAGAGATGCCTGCATTCTCAGGTTTAT T A MYCBP2 Ensembl:ENSG00000005810 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1402950855 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79007,RMVar_hsa_circ_122811,RMVar_hsa_circ_163820,RMVar_hsa_circ_163821,RMVar_hsa_circ_3612,RMVar_hsa_circ_109703,RMVar_hsa_circ_163845,RMVar_hsa_circ_100693,RMVar_hsa_circ_163851,RMVar_hsa_circ_113731,RMVar_hsa_circ_103365,RMVar_hsa_circ_92922,RMVar_hsa_circ_163857,RMVar_hsa_circ_163859,RMVar_hsa_circ_163858,RMVar_hsa_circ_82867,RMVar_hsa_circ_163871,RMVar_hsa_circ_3929,RMVar_hsa_circ_98933,RMVar_hsa_circ_163889,RMVar_hsa_circ_34792,RMVar_hsa_circ_319130,RMVar_hsa_circ_45187,RMVar_hsa_circ_163897,RMVar_hsa_circ_110510,RMVar_hsa_circ_325966,RMVar_hsa_circ_268533,RMVar_hsa_circ_9368,RMVar_hsa_circ_163908,RMVar_hsa_circ_334568,RMVar_hsa_circ_372437,RMVar_hsa_circ_54481,RMVar_hsa_circ_163909,RMVar_hsa_circ_163910,RMVar_hsa_circ_102095,RMVar_hsa_circ_106883,RMVar_hsa_circ_106679,RMVar_hsa_circ_163916,RMVar_hsa_circ_163917,RMVar_hsa_circ_163915,RMVar_hsa_circ_271716,RMVar_hsa_circ_280227,RMVar_hsa_circ_319100,RMVar_hsa_circ_72890,RMVar_hsa_circ_163920,RMVar_hsa_circ_163922,RMVar_hsa_circ_54122,RMVar_hsa_circ_163921,RMVar_hsa_circ_163923,RMVar_hsa_circ_38542,RMVar_hsa_circ_323919,RMVar_hsa_circ_341923,RMVar_hsa_circ_55439,RMVar_hsa_circ_163924 41952 RMVar_ID_41952 Human_SNP_ID_537028054 A-to-I Human chr13 - 77255175 77255175 77255175 GCAACTATGGAAAACATAGATTTTTCATTCGTATGAAGGTGACTCAAAAAACTGAAAATGGAGCT GCAACTATGGAAAACATAGATTTTTCATTCGTGTGAAGGTGACTCAAAAAACTGAAAATGGAGCT T C MYCBP2 Ensembl:ENSG00000005810 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs948263437 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79007,RMVar_hsa_circ_122811,RMVar_hsa_circ_163820,RMVar_hsa_circ_163821,RMVar_hsa_circ_3612,RMVar_hsa_circ_109703,RMVar_hsa_circ_163845,RMVar_hsa_circ_100693,RMVar_hsa_circ_163851,RMVar_hsa_circ_113731,RMVar_hsa_circ_103365,RMVar_hsa_circ_92922,RMVar_hsa_circ_163857,RMVar_hsa_circ_163859,RMVar_hsa_circ_163858,RMVar_hsa_circ_82867,RMVar_hsa_circ_163871,RMVar_hsa_circ_3929,RMVar_hsa_circ_98933,RMVar_hsa_circ_163889,RMVar_hsa_circ_34792,RMVar_hsa_circ_319130,RMVar_hsa_circ_45187,RMVar_hsa_circ_163897,RMVar_hsa_circ_110510,RMVar_hsa_circ_325966,RMVar_hsa_circ_268533,RMVar_hsa_circ_9368,RMVar_hsa_circ_163908,RMVar_hsa_circ_334568,RMVar_hsa_circ_372437,RMVar_hsa_circ_54481,RMVar_hsa_circ_163909,RMVar_hsa_circ_163910,RMVar_hsa_circ_102095,RMVar_hsa_circ_106883,RMVar_hsa_circ_106679,RMVar_hsa_circ_163916,RMVar_hsa_circ_163917,RMVar_hsa_circ_163915,RMVar_hsa_circ_271716,RMVar_hsa_circ_280227,RMVar_hsa_circ_319100,RMVar_hsa_circ_72890,RMVar_hsa_circ_163920,RMVar_hsa_circ_163922,RMVar_hsa_circ_54122,RMVar_hsa_circ_163921,RMVar_hsa_circ_163923,RMVar_hsa_circ_38542,RMVar_hsa_circ_323919,RMVar_hsa_circ_341923,RMVar_hsa_circ_55439,RMVar_hsa_circ_163924 41953 RMVar_ID_41953 Human_SNP_ID_537028449 A-to-I Human chr13 - 77257023 77257023 77257023 TTTATGGTTAAATAGTACTACCTTGTGTTTATATGCCACATTTTCTTTATCCACTCATCTGTTGA TTTATGGTTAAATAGTACTACCTTGTGTTTATGTGCCACATTTTCTTTATCCACTCATCTGTTGA T C MYCBP2 Ensembl:ENSG00000005810 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs927210436 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79007,RMVar_hsa_circ_122811,RMVar_hsa_circ_163820,RMVar_hsa_circ_163821,RMVar_hsa_circ_3612,RMVar_hsa_circ_109703,RMVar_hsa_circ_163845,RMVar_hsa_circ_100693,RMVar_hsa_circ_163851,RMVar_hsa_circ_113731,RMVar_hsa_circ_103365,RMVar_hsa_circ_92922,RMVar_hsa_circ_163857,RMVar_hsa_circ_163859,RMVar_hsa_circ_163858,RMVar_hsa_circ_82867,RMVar_hsa_circ_163871,RMVar_hsa_circ_3929,RMVar_hsa_circ_98933,RMVar_hsa_circ_163889,RMVar_hsa_circ_34792,RMVar_hsa_circ_319130,RMVar_hsa_circ_45187,RMVar_hsa_circ_163897,RMVar_hsa_circ_110510,RMVar_hsa_circ_325966,RMVar_hsa_circ_268533,RMVar_hsa_circ_9368,RMVar_hsa_circ_163908,RMVar_hsa_circ_334568,RMVar_hsa_circ_372437,RMVar_hsa_circ_54481,RMVar_hsa_circ_163909,RMVar_hsa_circ_163910,RMVar_hsa_circ_102095,RMVar_hsa_circ_106883,RMVar_hsa_circ_106679,RMVar_hsa_circ_163916,RMVar_hsa_circ_163917,RMVar_hsa_circ_163915,RMVar_hsa_circ_271716,RMVar_hsa_circ_280227,RMVar_hsa_circ_319100,RMVar_hsa_circ_72890,RMVar_hsa_circ_163920,RMVar_hsa_circ_163922,RMVar_hsa_circ_54122,RMVar_hsa_circ_163921,RMVar_hsa_circ_163923,RMVar_hsa_circ_38542,RMVar_hsa_circ_323919,RMVar_hsa_circ_341923,RMVar_hsa_circ_55439,RMVar_hsa_circ_163924 41954 RMVar_ID_41954 Human_SNP_ID_537028460 A-to-I Human chr13 - 77257062 77257062 77257062 TACATCCTTGTTGTTGCAAATGATAGGATCTCAGTGTTTTTTATGGTTAAATAGTACTACCTTGT TACATCCTTGTTGTTGCAAATGATAGGATCTCCGTGTTTTTTATGGTTAAATAGTACTACCTTGT T G MYCBP2 Ensembl:ENSG00000005810 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs181165441 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3435586 RMVar_hsa_circ_79007,RMVar_hsa_circ_122811,RMVar_hsa_circ_163820,RMVar_hsa_circ_163821,RMVar_hsa_circ_3612,RMVar_hsa_circ_109703,RMVar_hsa_circ_163845,RMVar_hsa_circ_100693,RMVar_hsa_circ_163851,RMVar_hsa_circ_113731,RMVar_hsa_circ_103365,RMVar_hsa_circ_92922,RMVar_hsa_circ_163857,RMVar_hsa_circ_163859,RMVar_hsa_circ_163858,RMVar_hsa_circ_82867,RMVar_hsa_circ_163871,RMVar_hsa_circ_3929,RMVar_hsa_circ_98933,RMVar_hsa_circ_163889,RMVar_hsa_circ_34792,RMVar_hsa_circ_319130,RMVar_hsa_circ_45187,RMVar_hsa_circ_163897,RMVar_hsa_circ_110510,RMVar_hsa_circ_325966,RMVar_hsa_circ_268533,RMVar_hsa_circ_9368,RMVar_hsa_circ_163908,RMVar_hsa_circ_334568,RMVar_hsa_circ_372437,RMVar_hsa_circ_54481,RMVar_hsa_circ_163909,RMVar_hsa_circ_163910,RMVar_hsa_circ_102095,RMVar_hsa_circ_106883,RMVar_hsa_circ_106679,RMVar_hsa_circ_163916,RMVar_hsa_circ_163917,RMVar_hsa_circ_163915,RMVar_hsa_circ_271716,RMVar_hsa_circ_280227,RMVar_hsa_circ_319100,RMVar_hsa_circ_72890,RMVar_hsa_circ_163920,RMVar_hsa_circ_163922,RMVar_hsa_circ_54122,RMVar_hsa_circ_163921,RMVar_hsa_circ_163923,RMVar_hsa_circ_38542,RMVar_hsa_circ_323919,RMVar_hsa_circ_341923,RMVar_hsa_circ_55439,RMVar_hsa_circ_163924 41955 RMVar_ID_41955 Human_SNP_ID_537028501 A-to-I Human chr13 - 77257226 77257226 77257226 CCCACTCTCCCTGACTACCCTTCCCAGTCTCTAGTAACCAGCATTGTACTCTCTATCTTCATGAG CCCACTCTCCCTGACTACCCTTCCCAGTCTCTGGTAACCAGCATTGTACTCTCTATCTTCATGAG T C MYCBP2 Ensembl:ENSG00000005810 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1376189920 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79007,RMVar_hsa_circ_122811,RMVar_hsa_circ_163820,RMVar_hsa_circ_163821,RMVar_hsa_circ_3612,RMVar_hsa_circ_109703,RMVar_hsa_circ_163845,RMVar_hsa_circ_100693,RMVar_hsa_circ_163851,RMVar_hsa_circ_113731,RMVar_hsa_circ_103365,RMVar_hsa_circ_92922,RMVar_hsa_circ_163857,RMVar_hsa_circ_163859,RMVar_hsa_circ_163858,RMVar_hsa_circ_82867,RMVar_hsa_circ_163871,RMVar_hsa_circ_3929,RMVar_hsa_circ_98933,RMVar_hsa_circ_163889,RMVar_hsa_circ_34792,RMVar_hsa_circ_319130,RMVar_hsa_circ_45187,RMVar_hsa_circ_163897,RMVar_hsa_circ_110510,RMVar_hsa_circ_325966,RMVar_hsa_circ_268533,RMVar_hsa_circ_9368,RMVar_hsa_circ_163908,RMVar_hsa_circ_334568,RMVar_hsa_circ_372437,RMVar_hsa_circ_54481,RMVar_hsa_circ_163909,RMVar_hsa_circ_163910,RMVar_hsa_circ_102095,RMVar_hsa_circ_106883,RMVar_hsa_circ_106679,RMVar_hsa_circ_163916,RMVar_hsa_circ_163917,RMVar_hsa_circ_163915,RMVar_hsa_circ_271716,RMVar_hsa_circ_280227,RMVar_hsa_circ_319100,RMVar_hsa_circ_72890,RMVar_hsa_circ_163920,RMVar_hsa_circ_163922,RMVar_hsa_circ_54122,RMVar_hsa_circ_163921,RMVar_hsa_circ_163923,RMVar_hsa_circ_38542,RMVar_hsa_circ_323919,RMVar_hsa_circ_341923,RMVar_hsa_circ_55439,RMVar_hsa_circ_163924 41956 RMVar_ID_41956 Human_SNP_ID_537033749 A-to-I Human chr13 - 77280503 77280503 77280503 GGTTGGTAGCAGAGTAAGCAATCTGAAAGAATAACAGAATATAGTAGTCTTCCATTGGCTTGAGA GGTTGGTAGCAGAGTAAGCAATCTGAAAGAATGACAGAATATAGTAGTCTTCCATTGGCTTGAGA T C MYCBP2 Ensembl:ENSG00000005810 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs8001793 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_124 GWAS_ID_4946,GWAS_ID_4947 RMVar_hsa_circ_122811,RMVar_hsa_circ_163821,RMVar_hsa_circ_3612,RMVar_hsa_circ_3929,RMVar_hsa_circ_34792,RMVar_hsa_circ_110510,RMVar_hsa_circ_9368,RMVar_hsa_circ_163908,RMVar_hsa_circ_372437,RMVar_hsa_circ_8468,RMVar_hsa_circ_163909,RMVar_hsa_circ_271716,RMVar_hsa_circ_280227,RMVar_hsa_circ_163922,RMVar_hsa_circ_163921,RMVar_hsa_circ_163923,RMVar_hsa_circ_323919,RMVar_hsa_circ_341923,RMVar_hsa_circ_163924,RMVar_hsa_circ_163925,RMVar_hsa_circ_338768,RMVar_hsa_circ_349831,RMVar_hsa_circ_163926,RMVar_hsa_circ_357022,RMVar_hsa_circ_359503,RMVar_hsa_circ_40784,RMVar_hsa_circ_163933,RMVar_hsa_circ_163932,RMVar_hsa_circ_275364,RMVar_hsa_circ_317175,RMVar_hsa_circ_344123,RMVar_hsa_circ_163934 41957 RMVar_ID_41957 Human_SNP_ID_537034609 A-to-I Human chr13 - 77284348 77284348 77284348 ACCTTCTCTGTGCCTCAGCCCCAAATGCTGCTATTATCCTAGTTTGCTCCTTTTCTTTGTTCCTC ACCTTCTCTGTGCCTCAGCCCCAAATGCTGCTTTTATCCTAGTTTGCTCCTTTTCTTTGTTCCTC T A MYCBP2 Ensembl:ENSG00000005810 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs9574027 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122811,RMVar_hsa_circ_163821,RMVar_hsa_circ_3612,RMVar_hsa_circ_3929,RMVar_hsa_circ_34792,RMVar_hsa_circ_110510,RMVar_hsa_circ_9368,RMVar_hsa_circ_163908,RMVar_hsa_circ_372437,RMVar_hsa_circ_8468,RMVar_hsa_circ_163909,RMVar_hsa_circ_271716,RMVar_hsa_circ_280227,RMVar_hsa_circ_163922,RMVar_hsa_circ_163921,RMVar_hsa_circ_163923,RMVar_hsa_circ_323919,RMVar_hsa_circ_341923,RMVar_hsa_circ_163924,RMVar_hsa_circ_163925,RMVar_hsa_circ_338768,RMVar_hsa_circ_349831,RMVar_hsa_circ_163926,RMVar_hsa_circ_357022,RMVar_hsa_circ_359503,RMVar_hsa_circ_40784,RMVar_hsa_circ_163933,RMVar_hsa_circ_163932,RMVar_hsa_circ_275364,RMVar_hsa_circ_317175,RMVar_hsa_circ_344123,RMVar_hsa_circ_163934 41958 RMVar_ID_41958 Human_SNP_ID_537034610 A-to-I Human chr13 - 77284348 77284348 77284348 ACCTTCTCTGTGCCTCAGCCCCAAATGCTGCTATTATCCTAGTTTGCTCCTTTTCTTTGTTCCTC ACCTTCTCTGTGCCTCAGCCCCAAATGCTGCTGTTATCCTAGTTTGCTCCTTTTCTTTGTTCCTC T C MYCBP2 Ensembl:ENSG00000005810 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs9574027 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122811,RMVar_hsa_circ_163821,RMVar_hsa_circ_3612,RMVar_hsa_circ_3929,RMVar_hsa_circ_34792,RMVar_hsa_circ_110510,RMVar_hsa_circ_9368,RMVar_hsa_circ_163908,RMVar_hsa_circ_372437,RMVar_hsa_circ_8468,RMVar_hsa_circ_163909,RMVar_hsa_circ_271716,RMVar_hsa_circ_280227,RMVar_hsa_circ_163922,RMVar_hsa_circ_163921,RMVar_hsa_circ_163923,RMVar_hsa_circ_323919,RMVar_hsa_circ_341923,RMVar_hsa_circ_163924,RMVar_hsa_circ_163925,RMVar_hsa_circ_338768,RMVar_hsa_circ_349831,RMVar_hsa_circ_163926,RMVar_hsa_circ_357022,RMVar_hsa_circ_359503,RMVar_hsa_circ_40784,RMVar_hsa_circ_163933,RMVar_hsa_circ_163932,RMVar_hsa_circ_275364,RMVar_hsa_circ_317175,RMVar_hsa_circ_344123,RMVar_hsa_circ_163934 41959 RMVar_ID_41959 Human_SNP_ID_537434353 A-to-I Human chr13 + 78909891 78909891 78909891 ACTTCTTCAGAACAACTTGCCTGCGGTTTGCTAGGTAGGAGGACCTGAAATTGAACTGATTGCCA ACTTCTTCAGAACAACTTGCCTGCGGTTTGCTGGGTAGGAGGACCTGAAATTGAACTGATTGCCA A G CCT5P2 Ensembl:ENSG00000230584 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417558050 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4274685 41960 RMVar_ID_41960 Human_SNP_ID_537434367 A-to-I Human chr13 + 78909926 78909926 78909926 TAGGAGGACCTGAAATTGAACTGATTGCCATCACAACAGGAGGGCAGATCATCACCAAGTTCTCA TAGGAGGACCTGAAATTGAACTGATTGCCATCGCAACAGGAGGGCAGATCATCACCAAGTTCTCA A G CCT5P2 Ensembl:ENSG00000230584 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs142579529 Functional Loss SNV dbSNP153 33..33 33 - - - 41961 RMVar_ID_41961 Human_SNP_ID_537546389 A-to-I Human chr13 - 79367388 79367388 79367388 TTTTTTTTTTTTTTGAGATGGAGTCTCCCCCTATACCCCAGGCTGGAGTGCAATGACACAGTCTC TTTTTTTTTTTTTTGAGATGGAGTCTCCCCCTTTACCCCAGGCTGGAGTGCAATGACACAGTCTC T A RBM26 Ensembl:ENSG00000139746 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7333651 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_4948,GWAS_ID_4949,GWAS_ID_4950 RMVar_hsa_circ_361603,RMVar_hsa_circ_347033,RMVar_hsa_circ_163963,RMVar_hsa_circ_163967,RMVar_hsa_circ_304663,RMVar_hsa_circ_163969,RMVar_hsa_circ_37458,RMVar_hsa_circ_163970,RMVar_hsa_circ_324647,RMVar_hsa_circ_60017,RMVar_hsa_circ_286731,RMVar_hsa_circ_20198,RMVar_hsa_circ_358456,RMVar_hsa_circ_285463,RMVar_hsa_circ_163972,RMVar_hsa_circ_163973,RMVar_hsa_circ_278270,RMVar_hsa_circ_360637,RMVar_hsa_circ_57738,RMVar_hsa_circ_13751,RMVar_hsa_circ_163974,RMVar_hsa_circ_120924,RMVar_hsa_circ_163976,RMVar_hsa_circ_92674,RMVar_hsa_circ_163977 41962 RMVar_ID_41962 Human_SNP_ID_537546390 A-to-I Human chr13 - 79367388 79367388 79367388 TTTTTTTTTTTTTTGAGATGGAGTCTCCCCCTATACCCCAGGCTGGAGTGCAATGACACAGTCTC TTTTTTTTTTTTTTGAGATGGAGTCTCCCCCTGTACCCCAGGCTGGAGTGCAATGACACAGTCTC T C RBM26 Ensembl:ENSG00000139746 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7333651 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_4948,GWAS_ID_4949,GWAS_ID_4950 RMVar_hsa_circ_361603,RMVar_hsa_circ_347033,RMVar_hsa_circ_163963,RMVar_hsa_circ_163967,RMVar_hsa_circ_304663,RMVar_hsa_circ_163969,RMVar_hsa_circ_37458,RMVar_hsa_circ_163970,RMVar_hsa_circ_324647,RMVar_hsa_circ_60017,RMVar_hsa_circ_286731,RMVar_hsa_circ_20198,RMVar_hsa_circ_358456,RMVar_hsa_circ_285463,RMVar_hsa_circ_163972,RMVar_hsa_circ_163973,RMVar_hsa_circ_278270,RMVar_hsa_circ_360637,RMVar_hsa_circ_57738,RMVar_hsa_circ_13751,RMVar_hsa_circ_163974,RMVar_hsa_circ_120924,RMVar_hsa_circ_163976,RMVar_hsa_circ_92674,RMVar_hsa_circ_163977 41963 RMVar_ID_41963 Human_SNP_ID_537546391 A-to-I Human chr13 - 79367388 79367388 79367388 TTTTTTTTTTTTTTGAGATGGAGTCTCCCCCTATACCCCAGGCTGGAGTGCAATGACACAGTCTC TTTTTTTTTTTTTTGAGATGGAGTCTCCCCCTCTACCCCAGGCTGGAGTGCAATGACACAGTCTC T G RBM26 Ensembl:ENSG00000139746 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7333651 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_4948,GWAS_ID_4949,GWAS_ID_4950 RMVar_hsa_circ_361603,RMVar_hsa_circ_347033,RMVar_hsa_circ_163963,RMVar_hsa_circ_163967,RMVar_hsa_circ_304663,RMVar_hsa_circ_163969,RMVar_hsa_circ_37458,RMVar_hsa_circ_163970,RMVar_hsa_circ_324647,RMVar_hsa_circ_60017,RMVar_hsa_circ_286731,RMVar_hsa_circ_20198,RMVar_hsa_circ_358456,RMVar_hsa_circ_285463,RMVar_hsa_circ_163972,RMVar_hsa_circ_163973,RMVar_hsa_circ_278270,RMVar_hsa_circ_360637,RMVar_hsa_circ_57738,RMVar_hsa_circ_13751,RMVar_hsa_circ_163974,RMVar_hsa_circ_120924,RMVar_hsa_circ_163976,RMVar_hsa_circ_92674,RMVar_hsa_circ_163977 41964 RMVar_ID_41964 Human_SNP_ID_537546755 A-to-I Human chr13 - 79368153 79368153 79368153 GGGCGTGGTGGCTGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAAGGCGTGAAA GGGCGTGGTGGCTGGCGCCTGTAGTCCCAGCTGCTCGGGAGGCTGAGGCAGGAGAAGGCGTGAAA T C RBM26 Ensembl:ENSG00000139746 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1196039154 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_361603,RMVar_hsa_circ_347033,RMVar_hsa_circ_163963,RMVar_hsa_circ_163967,RMVar_hsa_circ_304663,RMVar_hsa_circ_163969,RMVar_hsa_circ_37458,RMVar_hsa_circ_163970,RMVar_hsa_circ_324647,RMVar_hsa_circ_60017,RMVar_hsa_circ_286731,RMVar_hsa_circ_20198,RMVar_hsa_circ_358456,RMVar_hsa_circ_285463,RMVar_hsa_circ_163972,RMVar_hsa_circ_163973,RMVar_hsa_circ_278270,RMVar_hsa_circ_360637,RMVar_hsa_circ_57738,RMVar_hsa_circ_13751,RMVar_hsa_circ_163974,RMVar_hsa_circ_120924,RMVar_hsa_circ_163976,RMVar_hsa_circ_92674,RMVar_hsa_circ_163977 41965 RMVar_ID_41965 Human_SNP_ID_537546799 A-to-I Human chr13 - 79368285 79368285 79368285 GCAGCGGCTCACGCCTGTAATCCCAGCACTTTAGGAGGTTGAGGTGGGTGGATCATGAGGTCAGG GCAGCGGCTCACGCCTGTAATCCCAGCACTTTTGGAGGTTGAGGTGGGTGGATCATGAGGTCAGG T A RBM26 Ensembl:ENSG00000139746 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1402132820 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_361603,RMVar_hsa_circ_347033,RMVar_hsa_circ_163963,RMVar_hsa_circ_163967,RMVar_hsa_circ_304663,RMVar_hsa_circ_163969,RMVar_hsa_circ_37458,RMVar_hsa_circ_163970,RMVar_hsa_circ_324647,RMVar_hsa_circ_60017,RMVar_hsa_circ_286731,RMVar_hsa_circ_20198,RMVar_hsa_circ_358456,RMVar_hsa_circ_285463,RMVar_hsa_circ_163972,RMVar_hsa_circ_163973,RMVar_hsa_circ_278270,RMVar_hsa_circ_360637,RMVar_hsa_circ_57738,RMVar_hsa_circ_13751,RMVar_hsa_circ_163974,RMVar_hsa_circ_120924,RMVar_hsa_circ_163976,RMVar_hsa_circ_92674,RMVar_hsa_circ_163977 41966 RMVar_ID_41966 Human_SNP_ID_537546806 A-to-I Human chr13 - 79368299 79368299 79368299 ACTTTTGGCTGGGCGCAGCGGCTCACGCCTGTAATCCCAGCACTTTAGGAGGTTGAGGTGGGTGG ACTTTTGGCTGGGCGCAGCGGCTCACGCCTGTGATCCCAGCACTTTAGGAGGTTGAGGTGGGTGG T C RBM26 Ensembl:ENSG00000139746 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1181697030 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_361603,RMVar_hsa_circ_347033,RMVar_hsa_circ_163963,RMVar_hsa_circ_163967,RMVar_hsa_circ_304663,RMVar_hsa_circ_163969,RMVar_hsa_circ_37458,RMVar_hsa_circ_163970,RMVar_hsa_circ_324647,RMVar_hsa_circ_60017,RMVar_hsa_circ_286731,RMVar_hsa_circ_20198,RMVar_hsa_circ_358456,RMVar_hsa_circ_285463,RMVar_hsa_circ_163972,RMVar_hsa_circ_163973,RMVar_hsa_circ_278270,RMVar_hsa_circ_360637,RMVar_hsa_circ_57738,RMVar_hsa_circ_13751,RMVar_hsa_circ_163974,RMVar_hsa_circ_120924,RMVar_hsa_circ_163976,RMVar_hsa_circ_92674,RMVar_hsa_circ_163977 41967 RMVar_ID_41967 Human_SNP_ID_537547830 A-to-I Human chr13 - 79372037 79372037 79372037 CGACTTCGTGAACCACCCGCCTCAGCCTCCCAAAGTGCTGGCATTACAGGCATGAACCACTGTGC CGACTTCGTGAACCACCCGCCTCAGCCTCCCAGAGTGCTGGCATTACAGGCATGAACCACTGTGC T C RBM26 Ensembl:ENSG00000139746 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1352893880 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_361603,RMVar_hsa_circ_347033,RMVar_hsa_circ_163963,RMVar_hsa_circ_163967,RMVar_hsa_circ_304663,RMVar_hsa_circ_163969,RMVar_hsa_circ_37458,RMVar_hsa_circ_163970,RMVar_hsa_circ_324647,RMVar_hsa_circ_286731,RMVar_hsa_circ_20198,RMVar_hsa_circ_358456,RMVar_hsa_circ_163972,RMVar_hsa_circ_278270,RMVar_hsa_circ_57738,RMVar_hsa_circ_13751,RMVar_hsa_circ_163974,RMVar_hsa_circ_303703,RMVar_hsa_circ_339351,RMVar_hsa_circ_163981,RMVar_hsa_circ_163982,RMVar_hsa_circ_355571 41968 RMVar_ID_41968 Human_SNP_ID_537549015 A-to-I Human chr13 - 79374400 79374400 79374400 TCACTGCAACCTCTGCCTCCTGGGTTCAAGCAATTCTCCTCTCTCAGCCTCCCAAGTATCCCTCC TCACTGCAACCTCTGCCTCCTGGGTTCAAGCAGTTCTCCTCTCTCAGCCTCCCAAGTATCCCTCC T C RBM26 Ensembl:ENSG00000139746 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1461148860 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_361603,RMVar_hsa_circ_347033,RMVar_hsa_circ_163963,RMVar_hsa_circ_163967,RMVar_hsa_circ_304663,RMVar_hsa_circ_163969,RMVar_hsa_circ_37458,RMVar_hsa_circ_163970,RMVar_hsa_circ_324647,RMVar_hsa_circ_286731,RMVar_hsa_circ_20198,RMVar_hsa_circ_358456,RMVar_hsa_circ_163972,RMVar_hsa_circ_278270,RMVar_hsa_circ_57738,RMVar_hsa_circ_13751,RMVar_hsa_circ_163974,RMVar_hsa_circ_303703,RMVar_hsa_circ_339351,RMVar_hsa_circ_163981,RMVar_hsa_circ_163982,RMVar_hsa_circ_355571 41969 RMVar_ID_41969 Human_SNP_ID_537588476 A-to-I Human chr13 + 79537237 79537237 79537237 TCAAATGATTCTCCTGCCTTAGCCTCTTGAGTAGCTGGGACTACAGGAGCACGCCACCACATCTG TCAAATGATTCTCCTGCCTTAGCCTCTTGAGTGGCTGGGACTACAGGAGCACGCCACCACATCTG A G NDFIP2 Ensembl:ENSG00000102471 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs912963377 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40390,RMVar_hsa_circ_163987,RMVar_hsa_circ_127401,RMVar_hsa_circ_163985,RMVar_hsa_circ_163991,RMVar_hsa_circ_163988,RMVar_hsa_circ_320445,RMVar_hsa_circ_300456,RMVar_hsa_circ_76685,RMVar_hsa_circ_275960,RMVar_hsa_circ_163993,RMVar_hsa_circ_163994,RMVar_hsa_circ_163992,RMVar_hsa_circ_339201,RMVar_hsa_circ_74947,RMVar_hsa_circ_163996 41970 RMVar_ID_41970 Human_SNP_ID_537588477 A-to-I Human chr13 + 79537237 79537237 79537237 TCAAATGATTCTCCTGCCTTAGCCTCTTGAGTAGCTGGGACTACAGGAGCACGCCACCACATCTG TCAAATGATTCTCCTGCCTTAGCCTCTTGAGTTGCTGGGACTACAGGAGCACGCCACCACATCTG A T NDFIP2 Ensembl:ENSG00000102471 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs912963377 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40390,RMVar_hsa_circ_163987,RMVar_hsa_circ_127401,RMVar_hsa_circ_163985,RMVar_hsa_circ_163991,RMVar_hsa_circ_163988,RMVar_hsa_circ_320445,RMVar_hsa_circ_300456,RMVar_hsa_circ_76685,RMVar_hsa_circ_275960,RMVar_hsa_circ_163993,RMVar_hsa_circ_163994,RMVar_hsa_circ_163992,RMVar_hsa_circ_339201,RMVar_hsa_circ_74947,RMVar_hsa_circ_163996 41971 RMVar_ID_41971 Human_SNP_ID_537588479 A-to-I Human chr13 + 79537247 79537247 79537247 CTCCTGCCTTAGCCTCTTGAGTAGCTGGGACTACAGGAGCACGCCACCACATCTGGTTAATTTGT CTCCTGCCTTAGCCTCTTGAGTAGCTGGGACTGCAGGAGCACGCCACCACATCTGGTTAATTTGT A G NDFIP2 Ensembl:ENSG00000102471 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs927453721 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40390,RMVar_hsa_circ_163987,RMVar_hsa_circ_127401,RMVar_hsa_circ_163985,RMVar_hsa_circ_163991,RMVar_hsa_circ_163988,RMVar_hsa_circ_320445,RMVar_hsa_circ_300456,RMVar_hsa_circ_76685,RMVar_hsa_circ_275960,RMVar_hsa_circ_163993,RMVar_hsa_circ_163994,RMVar_hsa_circ_163992,RMVar_hsa_circ_339201,RMVar_hsa_circ_74947,RMVar_hsa_circ_163996 41972 RMVar_ID_41972 Human_SNP_ID_538669364 A-to-I Human chr13 - 83861111 83861111 83861111 AACAGTGTTGTCATTCATAGACGTCTATATCTATGAATATCTGTGAATGTCAATAAAAGACTGTA AACAGTGTTGTCATTCATAGACGTCTATATCTCTGAATATCTGTGAATGTCAATAAAAGACTGTA T G - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs938331751 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_164018 41973 RMVar_ID_41973 Human_SNP_ID_539266982 A-to-I Human chr13 + 86276144 86276144 86276144 TTACGAGATGACATAATTAGGCTTGATGATACAATGCACGTAGTGATTGCTACCCCTAGGAGAAT TTACGAGATGACATAATTAGGCTTGATGATACTATGCACGTAGTGATTGCTACCCCTAGGAGAAT A T DDX6P2 Ensembl:ENSG00000277914 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1316734523 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1474539 41974 RMVar_ID_41974 Human_SNP_ID_539641603 A-to-I Human chr13 + 87692742 87692742 87692742 GGCTGAAGCTTGAACCCGGAGGCAGCGGTTGCAGTGAGCTGAGATCGTGATACTGCACTCCAGCC GGCTGAAGCTTGAACCCGGAGGCAGCGGTTGCGGTGAGCTGAGATCGTGATACTGCACTCCAGCC A G SLITRK5 Ensembl:ENSG00000165300 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs567234927 Functional Loss SNV dbSNP153 33..33 33 - - - 41975 RMVar_ID_41975 Human_SNP_ID_653959327 A-to-I Human chr18 - 76805894 76805894 76805894 GGGAGGCTGAGGTTGCAGTGAGCCGAGATGACACCACTGGACTCCAGCCTGGGCTATAGAACAAG GGGAGGCTGAGGTTGCAGTGAGCCGAGATGACGCCACTGGACTCCAGCCTGGGCTATAGAACAAG T C ZNF236-DT Ensembl:ENSG00000264278 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs376702256 Functional Loss SNV dbSNP153 33..33 33 - - - 41976 RMVar_ID_41976 Human_SNP_ID_653961805 A-to-I Human chr18 - 76815796 76815796 76815796 GAACTCCTAGCCTCAAGGGATTCGCCTGCGTCAGCTTCCCAAAGTGCTGGGATTACAGGTGGCAG GAACTCCTAGCCTCAAGGGATTCGCCTGCGTCGGCTTCCCAAAGTGCTGGGATTACAGGTGGCAG T C ZNF236-DT Ensembl:ENSG00000264278 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910955667 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_190696 41977 RMVar_ID_41977 Human_SNP_ID_653961806 A-to-I Human chr18 - 76815796 76815796 76815796 GAACTCCTAGCCTCAAGGGATTCGCCTGCGTCAGCTTCCCAAAGTGCTGGGATTACAGGTGGCAG GAACTCCTAGCCTCAAGGGATTCGCCTGCGTCCGCTTCCCAAAGTGCTGGGATTACAGGTGGCAG T G ZNF236-DT Ensembl:ENSG00000264278 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910955667 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_190696 41978 RMVar_ID_41978 Human_SNP_ID_653963198 A-to-I Human chr18 - 76820388 76820388 76820388 TCTGCCTACTGCACTCTCTGCCTCCCCGGCTCAAGTGATCCTCCCACCTCAGCACCCCAAGTAGC TCTGCCTACTGCACTCTCTGCCTCCCCGGCTCGAGTGATCCTCCCACCTCAGCACCCCAAGTAGC T C ZNF236-DT Ensembl:ENSG00000264278 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1043477048 Functional Loss SNV dbSNP153 33..33 33 - - - 41979 RMVar_ID_41979 Human_SNP_ID_653963236 A-to-I Human chr18 - 76820469 76820469 76820469 TGTGTATGATGTTTGTTTGTTTGTTTGTTTTTAAGACAGGGTCAGGCTCTGTTGCCCCGGCTGGA TGTGTATGATGTTTGTTTGTTTGTTTGTTTTTTAGACAGGGTCAGGCTCTGTTGCCCCGGCTGGA T A ZNF236-DT Ensembl:ENSG00000264278 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs535425931 Functional Loss SNV dbSNP153 33..33 33 - - - 41980 RMVar_ID_41980 Human_SNP_ID_653965431 A-to-I Human chr18 + 76826688 76826688 76826688 AGGCATGGTGGCTGGCGCCTGTAGTCGCAGCTACTTGGGAGTGCTGAGGCATGAGAATCGCTTGA AGGCATGGTGGCTGGCGCCTGTAGTCGCAGCTGCTTGGGAGTGCTGAGGCATGAGAATCGCTTGA A G ZNF236 Ensembl:ENSG00000130856 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs926802214 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13338572 RMVar_hsa_circ_99981,RMVar_hsa_circ_101010,RMVar_hsa_circ_190699,RMVar_hsa_circ_190700 41981 RMVar_ID_41981 Human_SNP_ID_653965651 A-to-I Human chr18 + 76827393 76827393 76827393 TATTTTTAGTAGAGATGGGGTTTCACCCTGTTAGCTAGGATGGTCTCGAACTCCTGACCTCGTGA TATTTTTAGTAGAGATGGGGTTTCACCCTGTTGGCTAGGATGGTCTCGAACTCCTGACCTCGTGA A G ZNF236 Ensembl:ENSG00000130856 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1265893394 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99981,RMVar_hsa_circ_101010,RMVar_hsa_circ_190699,RMVar_hsa_circ_190700 41982 RMVar_ID_41982 Human_SNP_ID_653965652 A-to-I Human chr18 + 76827393 76827393 76827393 TATTTTTAGTAGAGATGGGGTTTCACCCTGTTAGCTAGGATGGTCTCGAACTCCTGACCTCGTGA TATTTTTAGTAGAGATGGGGTTTCACCCTGTTTGCTAGGATGGTCTCGAACTCCTGACCTCGTGA A T ZNF236 Ensembl:ENSG00000130856 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1265893394 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99981,RMVar_hsa_circ_101010,RMVar_hsa_circ_190699,RMVar_hsa_circ_190700 41983 RMVar_ID_41983 Human_SNP_ID_653970140 A-to-I Human chr18 + 76844160 76844160 76844160 TACTCTAGAGACTGATGCAGGAGAATTGCTTGAACCTGGGAGGTGGAGGTTGCAGTGAGTGGAGA TACTCTAGAGACTGATGCAGGAGAATTGCTTGCACCTGGGAGGTGGAGGTTGCAGTGAGTGGAGA A C ZNF236 Ensembl:ENSG00000130856 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985486263 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99981,RMVar_hsa_circ_101010,RMVar_hsa_circ_190699,RMVar_hsa_circ_190700 41984 RMVar_ID_41984 Human_SNP_ID_653970141 A-to-I Human chr18 + 76844160 76844160 76844160 TACTCTAGAGACTGATGCAGGAGAATTGCTTGAACCTGGGAGGTGGAGGTTGCAGTGAGTGGAGA TACTCTAGAGACTGATGCAGGAGAATTGCTTGGACCTGGGAGGTGGAGGTTGCAGTGAGTGGAGA A G ZNF236 Ensembl:ENSG00000130856 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985486263 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99981,RMVar_hsa_circ_101010,RMVar_hsa_circ_190699,RMVar_hsa_circ_190700 41985 RMVar_ID_41985 Human_SNP_ID_653970968 A-to-I Human chr18 + 76847485 76847485 76847485 TTTATTTATTTTTATTTATTTATTTTTTTTTTAGGCAGAGTCTCACTCTTTCACCCAGGCTGGAG TTTATTTATTTTTATTTATTTATTTTTTTTTTGGGCAGAGTCTCACTCTTTCACCCAGGCTGGAG A G ZNF236 Ensembl:ENSG00000130856 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1243413309 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6705873 RMVar_hsa_circ_99981,RMVar_hsa_circ_101010,RMVar_hsa_circ_190699,RMVar_hsa_circ_190700 41986 RMVar_ID_41986 Human_SNP_ID_653971069 A-to-I Human chr18 + 76847680 76847680 76847680 TTTAGTAGAGACAGGGTTTCACCGTGTTAGCCAGGATGGTCTTGATCTCCTGACTTCGTGTTCCA TTTAGTAGAGACAGGGTTTCACCGTGTTAGCCGGGATGGTCTTGATCTCCTGACTTCGTGTTCCA A G ZNF236 Ensembl:ENSG00000130856 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs540728246 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99981,RMVar_hsa_circ_101010,RMVar_hsa_circ_190699,RMVar_hsa_circ_190700 41987 RMVar_ID_41987 Human_SNP_ID_653971070 A-to-I Human chr18 + 76847680 76847680 76847680 TTTAGTAGAGACAGGGTTTCACCGTGTTAGCCAGGATGGTCTTGATCTCCTGACTTCGTGTTCCA TTTAGTAGAGACAGGGTTTCACCGTGTTAGCCTGGATGGTCTTGATCTCCTGACTTCGTGTTCCA A T ZNF236 Ensembl:ENSG00000130856 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs540728246 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99981,RMVar_hsa_circ_101010,RMVar_hsa_circ_190699,RMVar_hsa_circ_190700 41988 RMVar_ID_41988 Human_SNP_ID_654017049 A-to-I Human chr18 - 77027695 77027695 77027695 CAACTGAGCAAGACCCCATCTCTAAATAAATAAATAATTTTTTTCTGTCAAAATATCTGGTGGAC CAACTGAGCAAGACCCCATCTCTAAATAAATACATAATTTTTTTCTGTCAAAATATCTGGTGGAC T G MBP Ensembl:ENSG00000197971 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs891574565 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16219,RMVar_hsa_circ_363993 41989 RMVar_ID_41989 Human_SNP_ID_654027568 A-to-I Human chr18 - 77065778 77065778 77065778 TCCCTTCCCATCTCGGTTTTGTTTTTGCTCGCATGCCTTGTTGCACACATAGACATTCAGCATTT TCCCTTCCCATCTCGGTTTTGTTTTTGCTCGCGTGCCTTGTTGCACACATAGACATTCAGCATTT T C MBP Ensembl:ENSG00000197971 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs755865563 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16219,RMVar_hsa_circ_363993 41990 RMVar_ID_41990 Human_SNP_ID_654606248 A-to-I Human chr18 + 79163967 79163967 79163967 GAGACAGAAAAGGTCTCGCACTGTCCCAGGCTAGAGTGCTGTGGCTTAATCATAGCTCACTGCAG GAGACAGAAAAGGTCTCGCACTGTCCCAGGCTGGAGTGCTGTGGCTTAATCATAGCTCACTGCAG A G ATP9B Ensembl:ENSG00000166377 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1013029406 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_190768,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_292324,RMVar_hsa_circ_277353,RMVar_hsa_circ_190758,RMVar_hsa_circ_190756,RMVar_hsa_circ_190757,RMVar_hsa_circ_375502,RMVar_hsa_circ_335407,RMVar_hsa_circ_68975,RMVar_hsa_circ_38186,RMVar_hsa_circ_33147,RMVar_hsa_circ_190764,RMVar_hsa_circ_333566,RMVar_hsa_circ_276142,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_190770,RMVar_hsa_circ_190771,RMVar_hsa_circ_190769,RMVar_hsa_circ_190780,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_280634,RMVar_hsa_circ_190776,RMVar_hsa_circ_190777,RMVar_hsa_circ_190778,RMVar_hsa_circ_297801,RMVar_hsa_circ_345123,RMVar_hsa_circ_368894,RMVar_hsa_circ_287377,RMVar_hsa_circ_190782,RMVar_hsa_circ_59082,RMVar_hsa_circ_190781,RMVar_hsa_circ_190779 41991 RMVar_ID_41991 Human_SNP_ID_654664035 A-to-I Human chr18 - 79377794 79377794 79377794 TTCCCGCACTGAGAGGGAGGGGCCATCCCGGCATCTGTGCCCTGGGCTTGCCTAGCATGGGTGAA TTCCCGCACTGAGAGGGAGGGGCCATCCCGGCTTCTGTGCCCTGGGCTTGCCTAGCATGGGTGAA T A - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs536159627 Functional Loss SNV dbSNP153 33..33 33 - - - 41992 RMVar_ID_41992 Human_SNP_ID_654664036 A-to-I Human chr18 - 79377794 79377794 79377794 TTCCCGCACTGAGAGGGAGGGGCCATCCCGGCATCTGTGCCCTGGGCTTGCCTAGCATGGGTGAA TTCCCGCACTGAGAGGGAGGGGCCATCCCGGCCTCTGTGCCCTGGGCTTGCCTAGCATGGGTGAA T G - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs536159627 Functional Loss SNV dbSNP153 33..33 33 - - - 41993 RMVar_ID_41993 Human_SNP_ID_654854003 A-to-I Human chr18 + 79968406 79968406 79968406 TGGAGTGCAGTGGCATGATCTTGGCTCACTGCAAACTCCACCTCCCGGGTTTAAGCCATTCTCCT TGGAGTGCAGTGGCATGATCTTGGCTCACTGCCAACTCCACCTCCCGGGTTTAAGCCATTCTCCT A C HSBP1L1 Ensembl:ENSG00000226742 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs146059424 Functional Loss SNV dbSNP153 33..33 33 - - - 41994 RMVar_ID_41994 Human_SNP_ID_654854033 A-to-I Human chr18 - 79968525 79968525 79968525 GGTTGTGAGTTGGAGACCAGCCTGGCCAACATAGTGAAACCCCGTCTGTACTAAAATACAAAAAT GGTTGTGAGTTGGAGACCAGCCTGGCCAACATGGTGAAACCCCGTCTGTACTAAAATACAAAAAT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1568356061 Functional Loss SNV dbSNP153 33..33 33 - - - 41995 RMVar_ID_41995 Human_SNP_ID_654858328 A-to-I Human chr18 - 79983233 79983233 79983233 AGTTTGGGAAGCCGAGGCAGGCGAATCATCTGAGGTCAAGAGTTCGAGACCAGCTTGGCCAACAT AGTTTGGGAAGCCGAGGCAGGCGAATCATCTGCGGTCAAGAGTTCGAGACCAGCTTGGCCAACAT T G TXNL4A Ensembl:ENSG00000141759 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1447124376 Functional Loss SNV dbSNP153 33..33 33 - - - 41996 RMVar_ID_41996 Human_SNP_ID_654858338 A-to-I Human chr18 - 79983274 79983274 79983274 AATTTGAGGCCAGCGCCGTGGCTTAAACCTGTAATTCCAGCAGTTTGGGAAGCCGAGGCAGGCGA AATTTGAGGCCAGCGCCGTGGCTTAAACCTGTGATTCCAGCAGTTTGGGAAGCCGAGGCAGGCGA T C TXNL4A Ensembl:ENSG00000141759 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs985332697 Functional Loss SNV dbSNP153 33..33 33 - - - 41997 RMVar_ID_41997 Human_SNP_ID_654858343 A-to-I Human chr18 - 79983281 79983281 79983281 TAAAAACAATTTGAGGCCAGCGCCGTGGCTTAAACCTGTAATTCCAGCAGTTTGGGAAGCCGAGG TAAAAACAATTTGAGGCCAGCGCCGTGGCTTATACCTGTAATTCCAGCAGTTTGGGAAGCCGAGG T A TXNL4A Ensembl:ENSG00000141759 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1180900968 Functional Loss SNV dbSNP153 33..33 33 - - - 41998 RMVar_ID_41998 Human_SNP_ID_654858344 A-to-I Human chr18 - 79983281 79983281 79983281 TAAAAACAATTTGAGGCCAGCGCCGTGGCTTAAACCTGTAATTCCAGCAGTTTGGGAAGCCGAGG TAAAAACAATTTGAGGCCAGCGCCGTGGCTTACACCTGTAATTCCAGCAGTTTGGGAAGCCGAGG T G TXNL4A Ensembl:ENSG00000141759 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1180900968 Functional Loss SNV dbSNP153 33..33 33 - - - 41999 RMVar_ID_41999 Human_SNP_ID_654858682 A-to-I Human chr18 - 79984474 79984474 79984474 CTGCAACCTCAGCCTCCTGAGTAGCTGGGACTACAGGCCTGCACCACCACCACACCCTGCTAATT CTGCAACCTCAGCCTCCTGAGTAGCTGGGACTGCAGGCCTGCACCACCACCACACCCTGCTAATT T C TXNL4A Ensembl:ENSG00000141759 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025525489 Functional Loss SNV dbSNP153 33..33 33 - - - 42000 RMVar_ID_42000 Human_SNP_ID_654858747 A-to-I Human chr18 - 79984689 79984689 79984689 AGAGTATGAGCTCAGGAGGTCAAGGCTGCAGTAAGCTATCATCGTGCCGTTGCACTCCACCCTGG AGAGTATGAGCTCAGGAGGTCAAGGCTGCAGTCAGCTATCATCGTGCCGTTGCACTCCACCCTGG T G TXNL4A Ensembl:ENSG00000141759 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1267606392 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6707045,Human_RBP_ID_13340785 42001 RMVar_ID_42001 Human_SNP_ID_654875554 A-to-I Human chr18 + 80048051 80048051 80048051 TTTATGTACAAGAGACCTCCCCATCCTGATGTAGGAAATGAATGGTGATGATTTACGAGCGCAAC TTTATGTACAAGAGACCTCCCCATCCTGATGTGGGAAATGAATGGTGATGATTTACGAGCGCAAC A G RBFADN,RBFA,AC090360.1 Ensembl:ENSG00000261126,Ensembl:ENSG00000101546,Ensembl:ENSG00000267127 lincRNA,Protein coding,Protein coding intron,3'UTR,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1261387084 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_190821 42002 RMVar_ID_42002 Human_SNP_ID_654894177 A-to-I Human chr18 + 80120820 80120818 80120821 GGGATTACAGGCACGTACCACCAAGTCCAACTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCA GGGATTACAGGCACGTACCACCAAGTCCAAC___TTTTTGTATTTTTAGTAGAGATGGGGTTTCA CTAA C ADNP2 Ensembl:ENSG00000101544 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1364052958 Functional Loss DEL dbSNP153 32..34 33 - - - 42003 RMVar_ID_42003 Human_SNP_ID_654894178 A-to-I Human chr18 + 80120820 80120820 80120820 GGGATTACAGGCACGTACCACCAAGTCCAACTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCA GGGATTACAGGCACGTACCACCAAGTCCAACTCATTTTTGTATTTTTAGTAGAGATGGGGTTTCA A C ADNP2 Ensembl:ENSG00000101544 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1338575743 Functional Loss SNV dbSNP153 33..33 33 - - - 42004 RMVar_ID_42004 Human_SNP_ID_654894179 A-to-I Human chr18 + 80120820 80120820 80120820 GGGATTACAGGCACGTACCACCAAGTCCAACTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCA GGGATTACAGGCACGTACCACCAAGTCCAACTGATTTTTGTATTTTTAGTAGAGATGGGGTTTCA A G ADNP2 Ensembl:ENSG00000101544 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1338575743 Functional Loss SNV dbSNP153 33..33 33 - - - 42005 RMVar_ID_42005 Human_SNP_ID_654897547 A-to-I Human chr18 + 80132806 80132806 80132806 CCCAGGCTTGAGTGCAGCTCACTGCAACCTCCACCTCCCGGGTTCAAGCAATTCTCCTGCCTCAG CCCAGGCTTGAGTGCAGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGCAATTCTCCTGCCTCAG A G ADNP2 Ensembl:ENSG00000101544 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs930230295 Functional Loss SNV dbSNP153 33..33 33 - - - 42006 RMVar_ID_42006 Human_SNP_ID_654904663 A-to-I Human chr18 - 80158595 80158595 80158595 GATACGGTCCCCCCTCAGCCTCCAAAAATGCTAGGATTATAGACGTGAGCCACAGCACCAGACCA GATACGGTCCCCCCTCAGCCTCCAAAAATGCTGGGATTATAGACGTGAGCCACAGCACCAGACCA T C PARD6G Ensembl:ENSG00000178184 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs1335635079 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81005,RMVar_hsa_circ_190827 42007 RMVar_ID_42007 Human_SNP_ID_654904666 A-to-I Human chr18 - 80158603 80158603 80158603 CCTCAGGTGATACGGTCCCCCCTCAGCCTCCAAAAATGCTAGGATTATAGACGTGAGCCACAGCA CCTCAGGTGATACGGTCCCCCCTCAGCCTCCAGAAATGCTAGGATTATAGACGTGAGCCACAGCA T C PARD6G Ensembl:ENSG00000178184 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs114283276 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81005,RMVar_hsa_circ_190827 42008 RMVar_ID_42008 Human_SNP_ID_654904667 A-to-I Human chr18 - 80158603 80158603 80158603 CCTCAGGTGATACGGTCCCCCCTCAGCCTCCAAAAATGCTAGGATTATAGACGTGAGCCACAGCA CCTCAGGTGATACGGTCCCCCCTCAGCCTCCACAAATGCTAGGATTATAGACGTGAGCCACAGCA T G PARD6G Ensembl:ENSG00000178184 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs114283276 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81005,RMVar_hsa_circ_190827 42009 RMVar_ID_42009 Human_SNP_ID_654904696 A-to-I Human chr18 - 80158700 80158700 80158700 GCTGGGACAGGCACATGCCACCATACCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGATTTCA GCTGGGACAGGCACATGCCACCATACCCAGCTGATTTTTGTATTTTTAGTAGAGATGGGATTTCA T C PARD6G Ensembl:ENSG00000178184 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1000525495 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81005,RMVar_hsa_circ_190827 42010 RMVar_ID_42010 Human_SNP_ID_654922683 A-to-I Human chr18 - 80226352 80226352 80226352 AGCCTGACCAACATGGAGGAACCCCCGTCTCTACTAAAAATGCAAAATTAGCTGGGCGTGGTGGT AGCCTGACCAACATGGAGGAACCCCCGTCTCTGCTAAAAATGCAAAATTAGCTGGGCGTGGTGGT T C PARD6G Ensembl:ENSG00000178184 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs894917681 Functional Loss SNV dbSNP153 33..33 33 - - - 42011 RMVar_ID_42011 Human_SNP_ID_632727015 A-to-I Human chr17 + 75015857 75015857 75015857 TGTCCCAGGCAGGAGTGCAGTGTCCTGATCTCAGCTCACTGCAACCTCCATCTCCTGGGTTCAAG TGTCCCAGGCAGGAGTGCAGTGTCCTGATCTCGGCTCACTGCAACCTCCATCTCCTGGGTTCAAG A G MRPL58 Ensembl:ENSG00000167862 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1392643552 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78525,RMVar_hsa_circ_109022,RMVar_hsa_circ_186943,RMVar_hsa_circ_186944 42012 RMVar_ID_42012 Human_SNP_ID_632727029 A-to-I Human chr17 + 75015915 75015915 75015915 GTTCAAGCAATCCTGCCTCAGCCTCCCCCAGTAGCTAGGATTACAGGTGTGTGCCACCATGCCTA GTTCAAGCAATCCTGCCTCAGCCTCCCCCAGTGGCTAGGATTACAGGTGTGTGCCACCATGCCTA A G MRPL58 Ensembl:ENSG00000167862 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1230231674 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78525,RMVar_hsa_circ_109022,RMVar_hsa_circ_186943,RMVar_hsa_circ_186944 42013 RMVar_ID_42013 Human_SNP_ID_632732993 A-to-I Human chr17 + 75036287 75036287 75036287 TGGGGCTACAGGCGCCCGCCACCACACTGGCTAATTTTTTGTATTTTTAGTATAGACGGGGTTTC TGGGGCTACAGGCGCCCGCCACCACACTGGCTGATTTTTTGTATTTTTAGTATAGACGGGGTTTC A G KCTD2 Ensembl:ENSG00000180901 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1304308929 Functional Loss SNV dbSNP153 33..33 33 - - - 42014 RMVar_ID_42014 Human_SNP_ID_632738261 A-to-I Human chr17 + 75054117 75054117 75054117 ACAGCTCACTGCAGCCTTGGCTTCCCAGGCTCAGGTGATTTTCCTACCTCAGCCTACCGAGTAGC ACAGCTCACTGCAGCCTTGGCTTCCCAGGCTCGGGTGATTTTCCTACCTCAGCCTACCGAGTAGC A G KCTD2 Ensembl:ENSG00000180901 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1279504689 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120023,RMVar_hsa_circ_371497,RMVar_hsa_circ_186957,RMVar_hsa_circ_186958,RMVar_hsa_circ_117875,RMVar_hsa_circ_186959 42015 RMVar_ID_42015 Human_SNP_ID_632738264 A-to-I Human chr17 + 75054130 75054130 75054130 GCCTTGGCTTCCCAGGCTCAGGTGATTTTCCTACCTCAGCCTACCGAGTAGCTGGGACTACAGCT GCCTTGGCTTCCCAGGCTCAGGTGATTTTCCTGCCTCAGCCTACCGAGTAGCTGGGACTACAGCT A G KCTD2 Ensembl:ENSG00000180901 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs944119484 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120023,RMVar_hsa_circ_371497,RMVar_hsa_circ_186957,RMVar_hsa_circ_186958,RMVar_hsa_circ_117875,RMVar_hsa_circ_186959 42016 RMVar_ID_42016 Human_SNP_ID_632738265 A-to-I Human chr17 + 75054130 75054130 75054130 GCCTTGGCTTCCCAGGCTCAGGTGATTTTCCTACCTCAGCCTACCGAGTAGCTGGGACTACAGCT GCCTTGGCTTCCCAGGCTCAGGTGATTTTCCTTCCTCAGCCTACCGAGTAGCTGGGACTACAGCT A T KCTD2 Ensembl:ENSG00000180901 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs944119484 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120023,RMVar_hsa_circ_371497,RMVar_hsa_circ_186957,RMVar_hsa_circ_186958,RMVar_hsa_circ_117875,RMVar_hsa_circ_186959 42017 RMVar_ID_42017 Human_SNP_ID_632738770 A-to-I Human chr17 + 75055897 75055897 75055897 TACTAAAAATACGAAAATTGTCTGAGTGTGGTAGCGGGCGCCTATAATCCCAGCTACTTGGGAGG TACTAAAAATACGAAAATTGTCTGAGTGTGGTGGCGGGCGCCTATAATCCCAGCTACTTGGGAGG A G KCTD2 Ensembl:ENSG00000180901 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1236433553 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13157330 RMVar_hsa_circ_120023,RMVar_hsa_circ_371497,RMVar_hsa_circ_186957,RMVar_hsa_circ_186958,RMVar_hsa_circ_117875,RMVar_hsa_circ_186959 42018 RMVar_ID_42018 Human_SNP_ID_632738776 A-to-I Human chr17 + 75055908 75055908 75055908 CGAAAATTGTCTGAGTGTGGTAGCGGGCGCCTATAATCCCAGCTACTTGGGAGGCTGAGGCAGGA CGAAAATTGTCTGAGTGTGGTAGCGGGCGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGA A G KCTD2 Ensembl:ENSG00000180901 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1384372151 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120023,RMVar_hsa_circ_371497,RMVar_hsa_circ_186957,RMVar_hsa_circ_186958,RMVar_hsa_circ_117875,RMVar_hsa_circ_186959 42019 RMVar_ID_42019 Human_SNP_ID_632739101 A-to-I Human chr17 + 75057215 75057215 75057215 ATCTTAGGCGAGCCACCAACCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCAACCATAC ATCTTAGGCGAGCCACCAACCTCAGCCTCCCAGAGTGCTGGGATTACAGGCGTGAGCAACCATAC A G KCTD2 Ensembl:ENSG00000180901 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs971860910 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120023,RMVar_hsa_circ_371497,RMVar_hsa_circ_186957,RMVar_hsa_circ_186958,RMVar_hsa_circ_117875,RMVar_hsa_circ_186959 42020 RMVar_ID_42020 Human_SNP_ID_632750777 A-to-I Human chr17 + 75099440 75099439 75099441 AATCCAATTTGGGGTTTGTTTGTTTTTGAGACAGAGTCTCACTCTGTTGCCCAGGCTGGAGTGCA AATCCAATTTGGGGTTTGTTTGTTTTTGAGAC__AGTCTCACTCTGTTGCCCAGGCTGGAGTGCA CAG C SLC16A5 Ensembl:ENSG00000170190 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 31158229,32596459 RNA-Seq:(High) rs1219454205 Functional Loss DEL dbSNP153 33..34 33 - - - 42021 RMVar_ID_42021 Human_SNP_ID_632750809 A-to-I Human chr17 + 75099585 75099585 75099585 TGACTCAGCCTCCTAGGTAGCTATTACAGACTACAGGCGCCTGCCACTAAGCCTGGCTAATTTTT TGACTCAGCCTCCTAGGTAGCTATTACAGACTGCAGGCGCCTGCCACTAAGCCTGGCTAATTTTT A G SLC16A5 Ensembl:ENSG00000170190 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs577951917 Functional Loss SNV dbSNP153 33..33 33 - - - 42022 RMVar_ID_42022 Human_SNP_ID_632750825 A-to-I Human chr17 + 75099622 75099622 75099622 CGCCTGCCACTAAGCCTGGCTAATTTTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGG CGCCTGCCACTAAGCCTGGCTAATTTTTTTGTGTTTTTAGTAGAGATGGGGTTTCACCATGTTGG A G SLC16A5 Ensembl:ENSG00000170190 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1268294490 Functional Loss SNV dbSNP153 33..33 33 - - - 42023 RMVar_ID_42023 Human_SNP_ID_632756681 A-to-I Human chr17 + 75119729 75119729 75119729 TGATCCGCCTGCCTCGGCCCTCTCAAAGTGCTAGGATTACAGGCGTGAGCCACCACGCCCAGCCT TGATCCGCCTGCCTCGGCCCTCTCAAAGTGCTGGGATTACAGGCGTGAGCCACCACGCCCAGCCT A G ARMC7 Ensembl:ENSG00000125449 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs896291382 Functional Loss SNV dbSNP153 33..33 33 - - - 42024 RMVar_ID_42024 Human_SNP_ID_632762184 A-to-I Human chr17 - 75137629 75137629 75137629 GAAGGTGGCTCATGCCTGTGATCCCAGCACTTAGGGAGGGTGAGATGGGAGGATCACTTGAGTCC GAAGGTGGCTCATGCCTGTGATCCCAGCACTTGGGGAGGGTGAGATGGGAGGATCACTTGAGTCC T C JPT1 Ensembl:ENSG00000189159 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1319897377 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111684,RMVar_hsa_circ_186965,RMVar_hsa_circ_81454,RMVar_hsa_circ_186964 42025 RMVar_ID_42025 Human_SNP_ID_632762355 A-to-I Human chr17 - 75138112 75138112 75138112 ACTAAAAATACAAAAAATTAGTCGGGCGTTGTAGCGGGCACCTATAATCCCAGCTACTTACTTGG ACTAAAAATACAAAAAATTAGTCGGGCGTTGTTGCGGGCACCTATAATCCCAGCTACTTACTTGG T A JPT1 Ensembl:ENSG00000189159 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1034038630 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6642541,Human_RBP_ID_13157625,Human_RBP_ID_18708270 RMVar_hsa_circ_111684,RMVar_hsa_circ_186965,RMVar_hsa_circ_81454,RMVar_hsa_circ_186964 42026 RMVar_ID_42026 Human_SNP_ID_632762463 A-to-I Human chr17 - 75138548 75138548 75138548 AAAAAATTAGCTGGGCATGGTGGCGGGCGCCTATAACCCCAGCTATTGGGAGGCTGAGGCAGGAG AAAAAATTAGCTGGGCATGGTGGCGGGCGCCTGTAACCCCAGCTATTGGGAGGCTGAGGCAGGAG T C AC022211.4,JPT1 Ensembl:ENSG00000265800,Ensembl:ENSG00000189159 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1404102886 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111684,RMVar_hsa_circ_186965,RMVar_hsa_circ_81454,RMVar_hsa_circ_186964 42027 RMVar_ID_42027 Human_SNP_ID_632762994 A-to-I Human chr17 - 75140717 75140717 75140717 TCATGTTGATCTTCCTGCCTTGGCCTCCCAAAATTCTGGGATTACAGGTGTGAGCCGCTGTGCCT TCATGTTGATCTTCCTGCCTTGGCCTCCCAAAGTTCTGGGATTACAGGTGTGAGCCGCTGTGCCT T C AC022211.4,JPT1 Ensembl:ENSG00000265800,Ensembl:ENSG00000189159 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs893118687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13157724 RMVar_hsa_circ_111684,RMVar_hsa_circ_186965,RMVar_hsa_circ_81454,RMVar_hsa_circ_186964 42028 RMVar_ID_42028 Human_SNP_ID_632763012 A-to-I Human chr17 - 75140785 75140785 75140785 GCTTGGCCAATTTTTGTAGTTTCTGTAGAGACAGGGTTTTGCTATGTTTCCCCCGGCTGGTCCTG GCTTGGCCAATTTTTGTAGTTTCTGTAGAGACGGGGTTTTGCTATGTTTCCCCCGGCTGGTCCTG T C AC022211.4,JPT1 Ensembl:ENSG00000265800,Ensembl:ENSG00000189159 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1456231102 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13157731 RMVar_hsa_circ_111684,RMVar_hsa_circ_186965,RMVar_hsa_circ_81454,RMVar_hsa_circ_186964 42029 RMVar_ID_42029 Human_SNP_ID_632763024 A-to-I Human chr17 - 75140835 75140835 75140835 CACCTGCCTTGGCCTCCCAAAGTGTCGGGATTACAGGCGTGAGCCACCGTGCTTGGCCAATTTTT CACCTGCCTTGGCCTCCCAAAGTGTCGGGATTGCAGGCGTGAGCCACCGTGCTTGGCCAATTTTT T C AC022211.4,JPT1 Ensembl:ENSG00000265800,Ensembl:ENSG00000189159 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1249731717 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111684,RMVar_hsa_circ_186965,RMVar_hsa_circ_81454,RMVar_hsa_circ_186964 42030 RMVar_ID_42030 Human_SNP_ID_632763335 A-to-I Human chr17 - 75141947 75141947 75141947 CTCCCGCCTTAGCCTCCTGAGTATCTGGGACTACAGGTGTGCGCCACTACAGCTGGCTATTTTTT CTCCCGCCTTAGCCTCCTGAGTATCTGGGACTGCAGGTGTGCGCCACTACAGCTGGCTATTTTTT T C JPT1 Ensembl:ENSG00000189159 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs997381727 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111684,RMVar_hsa_circ_186965,RMVar_hsa_circ_81454,RMVar_hsa_circ_186964 42031 RMVar_ID_42031 Human_SNP_ID_632763351 A-to-I Human chr17 - 75141993 75141993 75141993 ATGATCTCAGCTCAAGGCAACCTCCGCCTCCCAGGTTCAAGCGATTCTCCCGCCTTAGCCTCCTG ATGATCTCAGCTCAAGGCAACCTCCGCCTCCCGGGTTCAAGCGATTCTCCCGCCTTAGCCTCCTG T C JPT1 Ensembl:ENSG00000189159 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1402053022 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111684,RMVar_hsa_circ_186965,RMVar_hsa_circ_81454,RMVar_hsa_circ_186964 42032 RMVar_ID_42032 Human_SNP_ID_632763520 A-to-I Human chr17 - 75142552 75142552 75142552 CCTCCCTCTCCCCTCCCCTCCCCCCTTGACGGAGTTTAGCTCTTGTTGTCCAGGCTGGAGTGTAG CCTCCCTCTCCCCTCCCCTCCCCCCTTGACGGCGTTTAGCTCTTGTTGTCCAGGCTGGAGTGTAG T G JPT1 Ensembl:ENSG00000189159 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1452848206 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3543249,Human_RBP_ID_5129225,Human_RBP_ID_5318577,Human_RBP_ID_17079745,Human_RBP_ID_17565620,Human_RBP_ID_18942099 RMVar_hsa_circ_111684,RMVar_hsa_circ_186965,RMVar_hsa_circ_81454,RMVar_hsa_circ_186964 42033 RMVar_ID_42033 Human_SNP_ID_632764169 A-to-I Human chr17 - 75144425 75144425 75144425 TCACTGCAACTTCAAACTCCTGAGCTGAAGCAATCCTCCTGCCTCAGCCTCCTGAGTAGCTGGGA TCACTGCAACTTCAAACTCCTGAGCTGAAGCAGTCCTCCTGCCTCAGCCTCCTGAGTAGCTGGGA T C JPT1 Ensembl:ENSG00000189159 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1437327852 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111684,RMVar_hsa_circ_186965,RMVar_hsa_circ_81454,RMVar_hsa_circ_186964 42034 RMVar_ID_42034 Human_SNP_ID_632766155 A-to-I Human chr17 - 75151413 75151413 75151413 GACCTTGTGATCTGCCTGCCTTGGCTTCTCAAAGTGCTAGGATTACAGGCATGAGCCACCGCTCC GACCTTGTGATCTGCCTGCCTTGGCTTCTCAAGGTGCTAGGATTACAGGCATGAGCCACCGCTCC T C JPT1 Ensembl:ENSG00000189159 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1274708790 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111684,RMVar_hsa_circ_186964 42035 RMVar_ID_42035 Human_SNP_ID_632768801 A-to-I Human chr17 - 75161053 75161053 75161053 AGGATCGCTTGAACCTAGGAGGCAGAGGTTGCAGCGAGCCGAGATCATGCCACTGCACTCCAGCC AGGATCGCTTGAACCTAGGAGGCAGAGGTTGCCGCGAGCCGAGATCATGCCACTGCACTCCAGCC T G JPT1 Ensembl:ENSG00000189159 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1313236342 Functional Loss SNV dbSNP153 33..33 33 - - - 42036 RMVar_ID_42036 Human_SNP_ID_632769719 A-to-I Human chr17 - 75163809 75163809 75163809 TAGTTCCAGCTACTCTGAAGGCTGAGGTGAGAAGATTGCCTGAGCTCGGGGGGAGGCCGAGGCTG TAGTTCCAGCTACTCTGAAGGCTGAGGTGAGAGGATTGCCTGAGCTCGGGGGGAGGCCGAGGCTG T C JPT1 Ensembl:ENSG00000189159 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1346675601 Functional Loss SNV dbSNP153 33..33 33 - - - 42037 RMVar_ID_42037 Human_SNP_ID_632770492 A-to-I Human chr17 - 75166423 75166423 75166423 TTGCCCCAACTGGAGACCAATGACATGATCTCAGCTCACTGCAACCTCCGCCTCCCGGGTTCAAC TTGCCCCAACTGGAGACCAATGACATGATCTCGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAC T C JPT1,SUMO2 Ensembl:ENSG00000189159,Ensembl:ENSG00000188612 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1241768490 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13158376 42038 RMVar_ID_42038 Human_SNP_ID_632771456 A-to-I Human chr17 - 75169658 75169658 75169658 TATTTTTAGGCCGGGTGCAGTGGTTCACGCCTATAATCCCAGCATTTTGGGAGGCCGAGGAGGGT TATTTTTAGGCCGGGTGCAGTGGTTCACGCCTGTAATCCCAGCATTTTGGGAGGCCGAGGAGGGT T C SUMO2 Ensembl:ENSG00000188612 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1456810301 Functional Loss SNV dbSNP153 33..33 33 - - - 42039 RMVar_ID_42039 Human_SNP_ID_632771488 A-to-I Human chr17 - 75169789 75169777 75169789 GTTGGAGTCCAGTGGCACAATCTTGGCTCACCACAACCTCTGCTTCCTGGGTTCAAGCGATTCTC GTTGGAGTCCAGTGGCACAATCTTGGCTCACC____________TCCTGGGTTCAAGCGATTCTC AAGCAGAGGTTGT A SUMO2 Ensembl:ENSG00000188612 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1443953286 Functional Loss DEL dbSNP153 33..44 33 - - - 42040 RMVar_ID_42040 Human_SNP_ID_632771494 A-to-I Human chr17 - 75169789 75169789 75169789 GTTGGAGTCCAGTGGCACAATCTTGGCTCACCACAACCTCTGCTTCCTGGGTTCAAGCGATTCTC GTTGGAGTCCAGTGGCACAATCTTGGCTCACCGCAACCTCTGCTTCCTGGGTTCAAGCGATTCTC T C SUMO2 Ensembl:ENSG00000188612 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1472271137 Functional Loss SNV dbSNP153 33..33 33 - - - 42041 RMVar_ID_42041 Human_SNP_ID_632771584 A-to-I Human chr17 - 75169972 75169972 75169972 TTTTGTATTTTTAGTAGAGACTGGGTTTCACCATTTTGGCCAGGCTGGTCTTGAACTCCCGACCT TTTTGTATTTTTAGTAGAGACTGGGTTTCACCGTTTTGGCCAGGCTGGTCTTGAACTCCCGACCT T C SUMO2 Ensembl:ENSG00000188612 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs978119980 Functional Loss SNV dbSNP153 33..33 33 - - - 42042 RMVar_ID_42042 Human_SNP_ID_632772657 A-to-I Human chr17 - 75173359 75173359 75173359 GGCCAGGAGTTTAAGACCAGTCTGGGCAATATAGCAAGACCTGGTCTCTACAGGAAAGAAAAAGA GGCCAGGAGTTTAAGACCAGTCTGGGCAATATGGCAAGACCTGGTCTCTACAGGAAAGAAAAAGA T C SUMO2 Ensembl:ENSG00000188612 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1342746885 Functional Loss SNV dbSNP153 33..33 33 - - - 42043 RMVar_ID_42043 Human_SNP_ID_632774568 A-to-I Human chr17 - 75179428 75179428 75179428 TGCCTCCCGAGACCAAGCGATTCTCCTGTCTCAGTCTCCCGAGTAGGTGGGACTACGGGCGCACG TGCCTCCCGAGACCAAGCGATTCTCCTGTCTCCGTCTCCCGAGTAGGTGGGACTACGGGCGCACG T G SUMO2 Ensembl:ENSG00000188612 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs190660346 Functional Loss SNV dbSNP153 33..33 33 - - - 42044 RMVar_ID_42044 Human_SNP_ID_632781936 A-to-I Human chr17 - 75203394 75203394 75203394 AGGCACACGCCACTACGCCGGGCTAATTTTTTATTTTTTAGTAGAGACGGGGTTTCGCCATATTG AGGCACACGCCACTACGCCGGGCTAATTTTTTGTTTTTTAGTAGAGACGGGGTTTCGCCATATTG T C lnc-SUMO2-2 RNACentral:URS0000D58343 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1462554950 Functional Loss SNV dbSNP153 33..33 33 - - - 42045 RMVar_ID_42045 Human_SNP_ID_632783095 A-to-I Human chr17 + 75206772 75206772 75206772 CAGGCTGGAGTGCAGTGGCGCGGTCTCGGCTCACTGTAACCTCCGCCTCCCGGGTTCACACCATT CAGGCTGGAGTGCAGTGGCGCGGTCTCGGCTCCCTGTAACCTCCGCCTCCCGGGTTCACACCATT A C NUP85 Ensembl:ENSG00000125450 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs572492155 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13158975 42046 RMVar_ID_42046 Human_SNP_ID_632783096 A-to-I Human chr17 + 75206772 75206772 75206772 CAGGCTGGAGTGCAGTGGCGCGGTCTCGGCTCACTGTAACCTCCGCCTCCCGGGTTCACACCATT CAGGCTGGAGTGCAGTGGCGCGGTCTCGGCTCGCTGTAACCTCCGCCTCCCGGGTTCACACCATT A G NUP85 Ensembl:ENSG00000125450 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs572492155 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13158975 42047 RMVar_ID_42047 Human_SNP_ID_632783097 A-to-I Human chr17 + 75206772 75206772 75206772 CAGGCTGGAGTGCAGTGGCGCGGTCTCGGCTCACTGTAACCTCCGCCTCCCGGGTTCACACCATT CAGGCTGGAGTGCAGTGGCGCGGTCTCGGCTCTCTGTAACCTCCGCCTCCCGGGTTCACACCATT A T NUP85 Ensembl:ENSG00000125450 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs572492155 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13158975 42048 RMVar_ID_42048 Human_SNP_ID_632783284 A-to-I Human chr17 + 75207368 75207368 75207368 ACCATGCCCGGCTAATTTTGTATTTTTTTAGTAGAGACGAGGTTTCTCCATGTTGGTCAGGCTGG ACCATGCCCGGCTAATTTTGTATTTTTTTAGTGGAGACGAGGTTTCTCCATGTTGGTCAGGCTGG A G NUP85 Ensembl:ENSG00000125450 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1297588719 Functional Loss SNV dbSNP153 33..33 33 - - - 42049 RMVar_ID_42049 Human_SNP_ID_632783488 A-to-I Human chr17 + 75208180 75208180 75208180 TCAGCAGGGCGGGCACGGTGGCTCGCGCCTGTAGTCCTAGCACTTTGGGAGGCTGAGGCGGACGG TCAGCAGGGCGGGCACGGTGGCTCGCGCCTGTGGTCCTAGCACTTTGGGAGGCTGAGGCGGACGG A G NUP85 Ensembl:ENSG00000125450 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs976939530 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237760,Human_RBP_ID_13159015,Human_RBP_ID_17565623,Human_RBP_ID_22717502 Human_Splice_Rec_1864810 42050 RMVar_ID_42050 Human_SNP_ID_632783540 A-to-I Human chr17 + 75208338 75208338 75208338 GTGGTTGCACACACCTGTAGTCCCAGCTACTCAGGAGGTTGAGGCAGGAGAAGCCTTTGAACCCA GTGGTTGCACACACCTGTAGTCCCAGCTACTCGGGAGGTTGAGGCAGGAGAAGCCTTTGAACCCA A G NUP85 Ensembl:ENSG00000125450 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1305229955 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25324113 Human_Splice_Rec_1864811 42051 RMVar_ID_42051 Human_SNP_ID_632787911 A-to-I Human chr17 + 75224115 75224115 75224115 TCATCCAGGCTGGAGTGCAGTGGCACAATCTCAGCTCACTGCAACCTCCGCCGCCCAGATTCAAG TCATCCAGGCTGGAGTGCAGTGGCACAATCTCGGCTCACTGCAACCTCCGCCGCCCAGATTCAAG A G NUP85 Ensembl:ENSG00000125450 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1249713640 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37624,RMVar_hsa_circ_369057,RMVar_hsa_circ_330371,RMVar_hsa_circ_87064,RMVar_hsa_circ_83094,RMVar_hsa_circ_186976,RMVar_hsa_circ_357593,RMVar_hsa_circ_112245,RMVar_hsa_circ_93763,RMVar_hsa_circ_186977,RMVar_hsa_circ_186978,RMVar_hsa_circ_118140,RMVar_hsa_circ_24701,RMVar_hsa_circ_186982,RMVar_hsa_circ_186983 42052 RMVar_ID_42052 Human_SNP_ID_632788046 A-to-I Human chr17 + 75224711 75224710 75224711 AAAATTAGCTGGGCGTGATGGCATGCGCCTGTAATCTCAGCTACTCGGGAGGTTGAGACAGGAGA AAAATTAGCTGGGCGTGATGGCATGCGCCTGT_ATCTCAGCTACTCGGGAGGTTGAGACAGGAGA TA T NUP85 Ensembl:ENSG00000125450 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1183367714 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_37624,RMVar_hsa_circ_369057,RMVar_hsa_circ_330371,RMVar_hsa_circ_87064,RMVar_hsa_circ_83094,RMVar_hsa_circ_186976,RMVar_hsa_circ_357593,RMVar_hsa_circ_112245,RMVar_hsa_circ_93763,RMVar_hsa_circ_186977,RMVar_hsa_circ_186978,RMVar_hsa_circ_118140,RMVar_hsa_circ_24701,RMVar_hsa_circ_186982,RMVar_hsa_circ_186983 42053 RMVar_ID_42053 Human_SNP_ID_632788047 A-to-I Human chr17 + 75224711 75224711 75224711 AAAATTAGCTGGGCGTGATGGCATGCGCCTGTAATCTCAGCTACTCGGGAGGTTGAGACAGGAGA AAAATTAGCTGGGCGTGATGGCATGCGCCTGTCATCTCAGCTACTCGGGAGGTTGAGACAGGAGA A C NUP85 Ensembl:ENSG00000125450 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1435627198 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37624,RMVar_hsa_circ_369057,RMVar_hsa_circ_330371,RMVar_hsa_circ_87064,RMVar_hsa_circ_83094,RMVar_hsa_circ_186976,RMVar_hsa_circ_357593,RMVar_hsa_circ_112245,RMVar_hsa_circ_93763,RMVar_hsa_circ_186977,RMVar_hsa_circ_186978,RMVar_hsa_circ_118140,RMVar_hsa_circ_24701,RMVar_hsa_circ_186982,RMVar_hsa_circ_186983 42054 RMVar_ID_42054 Human_SNP_ID_632789756 A-to-I Human chr17 + 75230786 75230786 75230786 CATTCAAAAGCTACTTTCTAGCTGGGTGTGGTAGCGCATGCCTGTAATCTCAGCTACTGAAGAGG CATTCAAAAGCTACTTTCTAGCTGGGTGTGGTGGCGCATGCCTGTAATCTCAGCTACTGAAGAGG A G NUP85 Ensembl:ENSG00000125450 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs1179669048 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13160051,Human_RBP_ID_17566173 RMVar_hsa_circ_330371,RMVar_hsa_circ_96836,RMVar_hsa_circ_357593,RMVar_hsa_circ_112245,RMVar_hsa_circ_93763,RMVar_hsa_circ_186977,RMVar_hsa_circ_186983,RMVar_hsa_circ_98790,RMVar_hsa_circ_107434,RMVar_hsa_circ_116830,RMVar_hsa_circ_186987,RMVar_hsa_circ_186988,RMVar_hsa_circ_186991,RMVar_hsa_circ_100374,RMVar_hsa_circ_186992,RMVar_hsa_circ_186993 42055 RMVar_ID_42055 Human_SNP_ID_632796860 A-to-I Human chr17 - 75250506 75250506 75250506 CACCTGCCTTGGCCTCCCAAAGTGCTGAGATTACGGGCGTGAGCCACCGCATCCAGCCTGCTATG CACCTGCCTTGGCCTCCCAAAGTGCTGAGATTGCGGGCGTGAGCCACCGCATCCAGCCTGCTATG T C GGA3 Ensembl:ENSG00000125447 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs897423995 Functional Loss SNV dbSNP153 33..33 33 - - - 42056 RMVar_ID_42056 Human_SNP_ID_632797270 A-to-I Human chr17 - 75251851 75251851 75251851 GAAGAATCATCTGAGCCTGGGAAGTTGAGGCTACAGTGAAGCCATGATCGCACCACTGCACTCTT GAAGAATCATCTGAGCCTGGGAAGTTGAGGCTGCAGTGAAGCCATGATCGCACCACTGCACTCTT T C GGA3 Ensembl:ENSG00000125447 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs902364263 Functional Loss SNV dbSNP153 33..33 33 - - - 42057 RMVar_ID_42057 Human_SNP_ID_632804794 A-to-I Human chr17 - 75275720 75275720 75275720 GAACTCCTGACCTCAGTTGATCCGTCCGCCTCAGCCTCTCAAAGTGCTGGGATTACAGGCATGAG GAACTCCTGACCTCAGTTGATCCGTCCGCCTCGGCCTCTCAAAGTGCTGGGATTACAGGCATGAG T C SLC25A19 Ensembl:ENSG00000125454 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1245281983 Functional Loss SNV dbSNP153 33..33 33 - - - 42058 RMVar_ID_42058 Human_SNP_ID_632804835 A-to-I Human chr17 - 75275850 75275850 75275850 TCTCCTGCCTTGGCCTCCAAGCAGCTGGGATTACAGGCGCCCGCCACCATGTCCTAATTTTTGTA TCTCCTGCCTTGGCCTCCAAGCAGCTGGGATTTCAGGCGCCCGCCACCATGTCCTAATTTTTGTA T A SLC25A19 Ensembl:ENSG00000125454 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1168809427 Functional Loss SNV dbSNP153 33..33 33 - - - 42059 RMVar_ID_42059 Human_SNP_ID_632805041 A-to-I Human chr17 - 75276482 75276482 75276482 GCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAAACAGGAGAATCGCTTGAACGTGAGAGGTGGAT GCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGACAGGAGAATCGCTTGAACGTGAGAGGTGGAT T C SLC25A19 Ensembl:ENSG00000125454 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs572699463 Functional Loss SNV dbSNP153 33..33 33 - - - 42060 RMVar_ID_42060 Human_SNP_ID_632805044 A-to-I Human chr17 - 75276496 75276496 75276496 GGGTATGGTGGTGGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAAACAGGAGAATCGCTTGAA GGGTATGGTGGTGGGCGCCTGTAGTCCCAGCTCCTCGGGAGGCTGAAACAGGAGAATCGCTTGAA T G SLC25A19 Ensembl:ENSG00000125454 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1193056404 Functional Loss SNV dbSNP153 33..33 33 - - - 42061 RMVar_ID_42061 Human_SNP_ID_632807217 A-to-I Human chr17 - 75283947 75283947 75283947 ACCATGCCTGACTAATTTTTGTATTTTTAGTAAAGACAGGGTTTCACTATGTTGACCCGGCTGGT ACCATGCCTGACTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACTATGTTGACCCGGCTGGT T C SLC25A19 Ensembl:ENSG00000125454 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1417506193 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41815,RMVar_hsa_circ_352087,RMVar_hsa_circ_300175 42062 RMVar_ID_42062 Human_SNP_ID_632807246 A-to-I Human chr17 - 75284031 75284031 75284031 TTGGCTCAGTGCAGCTCTGCCTCCCGGGTTCAAGTGATTCTCCTGCCTCAGCCCCCCAAGTACCT TTGGCTCAGTGCAGCTCTGCCTCCCGGGTTCAGGTGATTCTCCTGCCTCAGCCCCCCAAGTACCT T C SLC25A19 Ensembl:ENSG00000125454 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs548876771 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41815,RMVar_hsa_circ_352087,RMVar_hsa_circ_300175 42063 RMVar_ID_42063 Human_SNP_ID_632807301 A-to-I Human chr17 - 75284218 75284218 75284218 TTGTATTTTTAGTAGAGACAGGGTTCCACCATATTGGCCAGGCTGGTCTCCAACTCCTGACCTCA TTGTATTTTTAGTAGAGACAGGGTTCCACCATGTTGGCCAGGCTGGTCTCCAACTCCTGACCTCA T C SLC25A19 Ensembl:ENSG00000125454 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1202975545 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41815,RMVar_hsa_circ_352087,RMVar_hsa_circ_300175 42064 RMVar_ID_42064 Human_SNP_ID_632807312 A-to-I Human chr17 - 75284246 75284246 75284246 GGCCCACGCCACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTCCACCATATTGG GGCCCACGCCACCATGCCTGGCTAATTTTTGTGTTTTTAGTAGAGACAGGGTTCCACCATATTGG T C SLC25A19 Ensembl:ENSG00000125454 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1264348737 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41815,RMVar_hsa_circ_352087,RMVar_hsa_circ_300175 42065 RMVar_ID_42065 Human_SNP_ID_632807489 A-to-I Human chr17 - 75284780 75284780 75284780 AAATTAGCTGGACATGGTGGCATGCGCCTGTAATCCCAGCTACTTGAGGAGCTGAGGTGAGAGGA AAATTAGCTGGACATGGTGGCATGCGCCTGTAGTCCCAGCTACTTGAGGAGCTGAGGTGAGAGGA T C SLC25A19 Ensembl:ENSG00000125454 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs932882847 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41815,RMVar_hsa_circ_352087,RMVar_hsa_circ_300175 42066 RMVar_ID_42066 Human_SNP_ID_632807505 A-to-I Human chr17 - 75284885 75284882 75284885 TAATCTCAGCCCTTTGGGAGCCCAAGGCGGGCAGATTGCTTGAGCTCAGGAGTTTGAGACCAGCC TAATCTCAGCCCTTTGGGAGCCCAAGGCGGGC___TTGCTTGAGCTCAGGAGTTTGAGACCAGCC ATCT A SLC25A19 Ensembl:ENSG00000125454 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1376790739 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_41815,RMVar_hsa_circ_352087,RMVar_hsa_circ_300175 42067 RMVar_ID_42067 Human_SNP_ID_632807506 A-to-I Human chr17 - 75284885 75284885 75284885 TAATCTCAGCCCTTTGGGAGCCCAAGGCGGGCAGATTGCTTGAGCTCAGGAGTTTGAGACCAGCC TAATCTCAGCCCTTTGGGAGCCCAAGGCGGGCGGATTGCTTGAGCTCAGGAGTTTGAGACCAGCC T C SLC25A19 Ensembl:ENSG00000125454 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1385139541 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41815,RMVar_hsa_circ_352087,RMVar_hsa_circ_300175 42068 RMVar_ID_42068 Human_SNP_ID_632808037 A-to-I Human chr17 - 75287009 75287009 75287009 TTTTGTAGAGTTGGGGTTTTGCAGTGTTGCCCAGGCTGGTCTTGAACTCCTGAGCTCAAGCAATC TTTTGTAGAGTTGGGGTTTTGCAGTGTTGCCCGGGCTGGTCTTGAACTCCTGAGCTCAAGCAATC T C SLC25A19 Ensembl:ENSG00000125454 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991686503 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_278505 42069 RMVar_ID_42069 Human_SNP_ID_632816977 A-to-I Human chr17 - 75320300 75320300 75320300 TGTAAAACACATACAAAAGAATTAAACCCACAAGCTGCCTCTGACAGCAGCCTGTGAGGGAGTGC TGTAAAACACATACAAAAGAATTAAACCCACAGGCTGCCTCTGACAGCAGCCTGTGAGGGAGTGC T C GRB2 Ensembl:ENSG00000177885 Protein coding intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1201227649 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1010446,Human_RBP_ID_1542020,Human_RBP_ID_6643305,Human_RBP_ID_8822139,Human_RBP_ID_9288194,Human_RBP_ID_17261907,Human_RBP_ID_17377578,Human_RBP_ID_17493945,Human_RBP_ID_22500401,Human_RBP_ID_27259635 42070 RMVar_ID_42070 Human_SNP_ID_632817796 A-to-I Human chr17 - 75323072 75323072 75323072 CTCTGTCGCACAGGCTGGAGTACAGTGGCCCAATCTCGGCTCACTGCAAGCTCCTCCTCCCGGGT CTCTGTCGCACAGGCTGGAGTACAGTGGCCCAGTCTCGGCTCACTGCAAGCTCCTCCTCCCGGGT T C GRB2 Ensembl:ENSG00000177885 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1285762161 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_187013,RMVar_hsa_circ_284216,RMVar_hsa_circ_292252,RMVar_hsa_circ_372398,RMVar_hsa_circ_187011,RMVar_hsa_circ_187012 42071 RMVar_ID_42071 Human_SNP_ID_632818049 A-to-I Human chr17 - 75323974 75323974 75323974 AACACTGTCCCTACTAAAAAAATACAAAAATTAGCCAGGCGTGGTGGCACATGCCTGTATTCCCA AACACTGTCCCTACTAAAAAAATACAAAAATTCGCCAGGCGTGGTGGCACATGCCTGTATTCCCA T G GRB2 Ensembl:ENSG00000177885 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs557253152 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_187013,RMVar_hsa_circ_284216,RMVar_hsa_circ_292252,RMVar_hsa_circ_372398,RMVar_hsa_circ_187011,RMVar_hsa_circ_187012 42072 RMVar_ID_42072 Human_SNP_ID_632819742 A-to-I Human chr17 - 75329721 75329720 75329721 TGCCTGGCTAATTTTTTATTTTTCGTAGAGACAGGGTCTCACTGTGTTGCCCGGGCTGGTCTTGA TGCCTGGCTAATTTTTTATTTTTCGTAGAGAC_GGGTCTCACTGTGTTGCCCGGGCTGGTCTTGA CT C GRB2 Ensembl:ENSG00000177885 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1376414945 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_13161085 RMVar_hsa_circ_187013,RMVar_hsa_circ_284216,RMVar_hsa_circ_372398,RMVar_hsa_circ_187012,RMVar_hsa_circ_330342 42073 RMVar_ID_42073 Human_SNP_ID_632819894 A-to-I Human chr17 - 75330351 75330351 75330351 TTTGAGATGGAGTCTCGCTCTGTCGCCAGGCTAGAGTGCTGTGGCGCGATCTCGGCTCACTGCAA TTTGAGATGGAGTCTCGCTCTGTCGCCAGGCTGGAGTGCTGTGGCGCGATCTCGGCTCACTGCAA T C GRB2 Ensembl:ENSG00000177885 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1236831633 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23749007 RMVar_hsa_circ_187013,RMVar_hsa_circ_284216,RMVar_hsa_circ_372398,RMVar_hsa_circ_187012,RMVar_hsa_circ_330342 42074 RMVar_ID_42074 Human_SNP_ID_632819943 A-to-I Human chr17 - 75330511 75330511 75330511 TGCCTCCACTCCCGTCGAATTGTTGTATTTTTAGTAGAGATGGGGTTTCACTGTGTTGGCCAAGC TGCCTCCACTCCCGTCGAATTGTTGTATTTTTGGTAGAGATGGGGTTTCACTGTGTTGGCCAAGC T C GRB2 Ensembl:ENSG00000177885 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs960824860 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_187013,RMVar_hsa_circ_284216,RMVar_hsa_circ_372398,RMVar_hsa_circ_187012,RMVar_hsa_circ_330342 42075 RMVar_ID_42075 Human_SNP_ID_632824454 A-to-I Human chr17 - 75346769 75346769 75346769 GTTAGGAGTTTGAGACTAGCCTGGCCAACATGATGAAACCCCGTCTCTACTAAAAAATACAAAAA GTTAGGAGTTTGAGACTAGCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAAATACAAAAA T C GRB2 Ensembl:ENSG00000177885 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs541236282 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_187013,RMVar_hsa_circ_372398,RMVar_hsa_circ_53079 42076 RMVar_ID_42076 Human_SNP_ID_632827157 A-to-I Human chr17 - 75356260 75356260 75356260 CTCTTGCCTCAGCTTCCCAAAGTGTTGGAATTACAGGCATGAACCACTGTACCTGGCCCAAATAT CTCTTGCCTCAGCTTCCCAAAGTGTTGGAATTGCAGGCATGAACCACTGTACCTGGCCCAAATAT T C GRB2 Ensembl:ENSG00000177885 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs896011093 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_187013,RMVar_hsa_circ_372398,RMVar_hsa_circ_53079 42077 RMVar_ID_42077 Human_SNP_ID_632829789 A-to-I Human chr17 - 75366682 75366682 75366682 CGTCAGCCTCCCAAGTAGCTGAAACTACAGGCATGCACTACCACACCCGGCTAATTTTTGTTTGT CGTCAGCCTCCCAAGTAGCTGAAACTACAGGCGTGCACTACCACACCCGGCTAATTTTTGTTTGT T C GRB2 Ensembl:ENSG00000177885 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1011182275 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_187013,RMVar_hsa_circ_372398,RMVar_hsa_circ_53079 42078 RMVar_ID_42078 Human_SNP_ID_632830097 A-to-I Human chr17 - 75368052 75368052 75368052 AAATTAGCCAGGCGTGGTGGCGAGTGCCTGTAATCCCAGCTGCTCCAGAGGCTGAGGCATGAGAA AAATTAGCCAGGCGTGGTGGCGAGTGCCTGTAGTCCCAGCTGCTCCAGAGGCTGAGGCATGAGAA T C GRB2 Ensembl:ENSG00000177885 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs983642077 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_187013,RMVar_hsa_circ_372398,RMVar_hsa_circ_53079 42079 RMVar_ID_42079 Human_SNP_ID_632831738 A-to-I Human chr17 - 75374352 75374352 75374352 TCTCCCAGGCTGGGGTGCAGTGGTGCGATCTCAGCTCACTGCAACCTCCGCCTCCCGGGTTCCAG TCTCCCAGGCTGGGGTGCAGTGGTGCGATCTCGGCTCACTGCAACCTCCGCCTCCCGGGTTCCAG T C GRB2 Ensembl:ENSG00000177885 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1335782665 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_187013,RMVar_hsa_circ_372398,RMVar_hsa_circ_53079 42080 RMVar_ID_42080 Human_SNP_ID_632831815 A-to-I Human chr17 - 75374533 75374533 75374533 GTGTCAATAGGATTTTTCCATGTTGCCAGGCTAATCTCAAACTCCTGAGCTAAAGTGATCCACCC GTGTCAATAGGATTTTTCCATGTTGCCAGGCTTATCTCAAACTCCTGAGCTAAAGTGATCCACCC T A GRB2 Ensembl:ENSG00000177885 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs940922483 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22475719,Human_RBP_ID_23749052 RMVar_hsa_circ_187013,RMVar_hsa_circ_372398,RMVar_hsa_circ_53079 42081 RMVar_ID_42081 Human_SNP_ID_632831998 A-to-I Human chr17 - 75375181 75375181 75375181 TATGTAGATCAGGCTAGCTGGCTCACATCTGTATTCCCAGCACTTTGGGAGGCTGAGGCAGGAAT TATGTAGATCAGGCTAGCTGGCTCACATCTGTGTTCCCAGCACTTTGGGAGGCTGAGGCAGGAAT T C GRB2 Ensembl:ENSG00000177885 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs546774350 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_187013,RMVar_hsa_circ_372398,RMVar_hsa_circ_53079 42082 RMVar_ID_42082 Human_SNP_ID_632832908 A-to-I Human chr17 - 75378207 75378207 75378207 TTTTGTATTTTTAGTAGAGACGGTGTTTCACCATGTTGGTCAGGCTGGTCTCGAACTCCTGACTG TTTTGTATTTTTAGTAGAGACGGTGTTTCACCGTGTTGGTCAGGCTGGTCTCGAACTCCTGACTG T C GRB2 Ensembl:ENSG00000177885 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1376084156 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_187013,RMVar_hsa_circ_372398,RMVar_hsa_circ_53079 42083 RMVar_ID_42083 Human_SNP_ID_632833254 A-to-I Human chr17 - 75379619 75379619 75379619 GAAGTGGGAGGACCACTTGAGCTCAGGAGTTCAAGACCAGCCTGGGCAACATAGCAAGACCCTGT GAAGTGGGAGGACCACTTGAGCTCAGGAGTTCGAGACCAGCCTGGGCAACATAGCAAGACCCTGT T C GRB2 Ensembl:ENSG00000177885 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1470523579 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_187013,RMVar_hsa_circ_372398,RMVar_hsa_circ_53079 42084 RMVar_ID_42084 Human_SNP_ID_632835391 A-to-I Human chr17 - 75387294 75387294 75387294 TGCTACCACACCCTGCTAATTTTTGTACTTTTAGTAGAGGTGAGTTTCACCATGTTGGCCAGGTT TGCTACCACACCCTGCTAATTTTTGTACTTTTGGTAGAGGTGAGTTTCACCATGTTGGCCAGGTT T C GRB2 Ensembl:ENSG00000177885 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs538542258 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13162167 RMVar_hsa_circ_187013,RMVar_hsa_circ_372398,RMVar_hsa_circ_53079 42085 RMVar_ID_42085 Human_SNP_ID_632853942 A-to-I Human chr17 + 75458618 75458618 75458618 GAGGTGGATGCCAGAGGATCGCTTGAGCCCAGAAGGTCGACGCTGCAGTGAGCTGTGATCATGCC GAGGTGGATGCCAGAGGATCGCTTGAGCCCAGGAGGTCGACGCTGCAGTGAGCTGTGATCATGCC A G TMEM94 Ensembl:ENSG00000177728 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264243060 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_187015,RMVar_hsa_circ_378011 42086 RMVar_ID_42086 Human_SNP_ID_632872172 A-to-I Human chr17 + 75519594 75519590 75519594 CATCTTTTCTTTTCTTTTTGAGACGGAGTCTCACTCTGTCGCCCAGGCTGTAGTGCAGTGGCATG CATCTTTTCTTTTCTTTTTGAGACGGAGT____CTCTGTCGCCCAGGCTGTAGTGCAGTGGCATG TCTCA T TSEN54 Ensembl:ENSG00000182173 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1243465016 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_116486,RMVar_hsa_circ_187042,RMVar_hsa_circ_371964,RMVar_hsa_circ_187045 42087 RMVar_ID_42087 Human_SNP_ID_632914757 A-to-I Human chr17 - 75657739 75657738 75657740 ACCTTTTTTTTTTTTTTTTTTTTTAAGAGACAAGGTCTCTCACTGTCACCCAGGCTAAAGTGCAG ACCTTTTTTTTTTTTTTTTTTTTTAAGAGAC__GGTCTCTCACTGTCACCCAGGCTAAAGTGCAG CTT C RECQL5 Ensembl:ENSG00000108469 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1377172161 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_117920,RMVar_hsa_circ_187057,RMVar_hsa_circ_28920,RMVar_hsa_circ_30440,RMVar_hsa_circ_292896,RMVar_hsa_circ_187058 42088 RMVar_ID_42088 Human_SNP_ID_632945267 A-to-I Human chr17 - 75762847 75762847 75762847 GGAGACCAGCCTGGTGCCACTCTCGGACCCCAAGCTGGCCGTGCTCATCACCAACTCTAATGTCC GGAGACCAGCCTGGTGCCACTCTCGGACCCCAGGCTGGCCGTGCTCATCACCAACTCTAATGTCC T C GALK1 Ensembl:ENSG00000108479 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1289749491 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_499940,Human_RBP_ID_897870 Human_Splice_Rec_1868818,Human_Splice_Rec_1868846,Human_Splice_Rec_1868860 RMVar_hsa_circ_126195,RMVar_hsa_circ_187089 42089 RMVar_ID_42089 Human_SNP_ID_632953365 A-to-I Human chr17 + 75787564 75787564 75787564 AAAAGAGACATGGGCAGGGTGCGGTTGCTCACACCTGTAATCCCAGCACTTTGGGAGCCTGAGGT AAAAGAGACATGGGCAGGGTGCGGTTGCTCACGCCTGTAATCCCAGCACTTTGGGAGCCTGAGGT A G UNK Ensembl:ENSG00000132478 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1400568850 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17566185,Human_RBP_ID_22586897 42090 RMVar_ID_42090 Human_SNP_ID_632953572 A-to-I Human chr17 + 75788345 75788345 75788345 GGGACTGCAGGCACACGCCACCATGGCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCA GGGACTGCAGGCACACGCCACCATGGCTGGCTGATTTTTGTATTTTTAGTAGAGACAGGGTTTCA A G UNK Ensembl:ENSG00000132478 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903122030 Functional Loss SNV dbSNP153 33..33 33 - - - 42091 RMVar_ID_42091 Human_SNP_ID_632954021 A-to-I Human chr17 + 75790222 75790222 75790222 CACACACTGAGGCAGGAGAATTGCTTGAACCCAGGAGGCGGGGGTTGCAGTGAGCCGAGATCTCG CACACACTGAGGCAGGAGAATTGCTTGAACCCGGGAGGCGGGGGTTGCAGTGAGCCGAGATCTCG A G UNK Ensembl:ENSG00000132478 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs371156744 Functional Loss SNV dbSNP153 33..33 33 - - - 42092 RMVar_ID_42092 Human_SNP_ID_632954066 A-to-I Human chr17 + 75790402 75790402 75790402 GCTATAGTCCCAACTCGTTGGGAAGCTGAGGCAGGAGGATCACTTGAGCCCAGGAGTTCCAGACC GCTATAGTCCCAACTCGTTGGGAAGCTGAGGCCGGAGGATCACTTGAGCCCAGGAGTTCCAGACC A C UNK Ensembl:ENSG00000132478 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs757623817 Functional Loss SNV dbSNP153 33..33 33 - - - 42093 RMVar_ID_42093 Human_SNP_ID_632954067 A-to-I Human chr17 + 75790402 75790402 75790402 GCTATAGTCCCAACTCGTTGGGAAGCTGAGGCAGGAGGATCACTTGAGCCCAGGAGTTCCAGACC GCTATAGTCCCAACTCGTTGGGAAGCTGAGGCGGGAGGATCACTTGAGCCCAGGAGTTCCAGACC A G UNK Ensembl:ENSG00000132478 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs757623817 Functional Loss SNV dbSNP153 33..33 33 - - - 42094 RMVar_ID_42094 Human_SNP_ID_632954955 A-to-I Human chr17 + 75794556 75794556 75794556 GCTACTAGGGAGGCTGAGGCAGGAGAATCACTAGGACCCAGGAGGCGCAGGTTGCGGTGAGCCGA GCTACTAGGGAGGCTGAGGCAGGAGAATCACTGGGACCCAGGAGGCGCAGGTTGCGGTGAGCCGA A G UNK Ensembl:ENSG00000132478 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1279860900 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6644201,Human_RBP_ID_13164752 42095 RMVar_ID_42095 Human_SNP_ID_632955127 A-to-I Human chr17 + 75795363 75795362 75795364 TTGTTGTTGTTGTTGTTTTTGGTTTTTGAGACAGGGTCTCGCTCTGTTGTCCAGGCTGGAGTGCA TTGTTGTTGTTGTTGTTTTTGGTTTTTGAGAC__GGTCTCGCTCTGTTGTCCAGGCTGGAGTGCA CAG C UNK Ensembl:ENSG00000132478 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1238297678 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_3537379 42096 RMVar_ID_42096 Human_SNP_ID_632955129 A-to-I Human chr17 + 75795363 75795363 75795363 TTGTTGTTGTTGTTGTTTTTGGTTTTTGAGACAGGGTCTCGCTCTGTTGTCCAGGCTGGAGTGCA TTGTTGTTGTTGTTGTTTTTGGTTTTTGAGACGGGGTCTCGCTCTGTTGTCCAGGCTGGAGTGCA A G UNK Ensembl:ENSG00000132478 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs897659217 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3537379 42097 RMVar_ID_42097 Human_SNP_ID_632955370 A-to-I Human chr17 + 75796367 75796367 75796367 TTGAGATATGGTCTTACTGTGTCACCCAGGCTAGAGTGCAGTGACGTAATCATAGCTCACTGCAG TTGAGATATGGTCTTACTGTGTCACCCAGGCTGGAGTGCAGTGACGTAATCATAGCTCACTGCAG A G UNK Ensembl:ENSG00000132478 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1381554640 Functional Loss SNV dbSNP153 33..33 33 - - - 42098 RMVar_ID_42098 Human_SNP_ID_632955567 A-to-I Human chr17 + 75797313 75797313 75797313 GCTGGAGTGCGGTGGCGCAATCTCGGCTCACTACAACCTCTGCCTCCCAGGCTCAAGCAGTTGTC GCTGGAGTGCGGTGGCGCAATCTCGGCTCACTGCAACCTCTGCCTCCCAGGCTCAAGCAGTTGTC A G UNK Ensembl:ENSG00000132478 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1182126892 Functional Loss SNV dbSNP153 33..33 33 - - - 42099 RMVar_ID_42099 Human_SNP_ID_632955908 A-to-I Human chr17 + 75798744 75798744 75798744 TTAATCTGTAGTGGCTGTGCATGGTGGCTCATACCTGTAATCCCAGCACTTTGAGAGACTAAAGA TTAATCTGTAGTGGCTGTGCATGGTGGCTCATCCCTGTAATCCCAGCACTTTGAGAGACTAAAGA A C UNK Ensembl:ENSG00000132478 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1405121839 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17566189 42100 RMVar_ID_42100 Human_SNP_ID_632956787 A-to-I Human chr17 + 75801903 75801903 75801903 ACAGAGTCTTGCTCTGATGCCCAGGCTGGAGTACAGTGGTGCGCTCAGCTCATTGCAACCTCAAC ACAGAGTCTTGCTCTGATGCCCAGGCTGGAGTGCAGTGGTGCGCTCAGCTCATTGCAACCTCAAC A G UNK Ensembl:ENSG00000132478 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1015996188 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_768524,Human_RBP_ID_13165060,Human_RBP_ID_17566191 42101 RMVar_ID_42101 Human_SNP_ID_632957210 A-to-I Human chr17 + 75803282 75803282 75803282 AAATTTAGCTGGGCATTGTGGCAGGCACCTGTAGTCCCAGCTACTTGGGAGCCTGAGGCAGAAGA AAATTTAGCTGGGCATTGTGGCAGGCACCTGTGGTCCCAGCTACTTGGGAGCCTGAGGCAGAAGA A G UNK Ensembl:ENSG00000132478 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1340589045 Functional Loss SNV dbSNP153 33..33 33 - - - 42102 RMVar_ID_42102 Human_SNP_ID_632958031 A-to-I Human chr17 + 75806252 75806252 75806252 CCGAGGCGGGCGGATCGCAAGTTCAGGAGATCAAGACCATCTGGCTAACATGGTGAAACCCCGTC CCGAGGCGGGCGGATCGCAAGTTCAGGAGATCGAGACCATCTGGCTAACATGGTGAAACCCCGTC A G UNK Ensembl:ENSG00000132478 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1350422835 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13165178 42103 RMVar_ID_42103 Human_SNP_ID_632958295 A-to-I Human chr17 + 75807266 75807266 75807266 GATGCCAGCTGGGAATAGTGGCGTATACCTGCAATCCCAGCTACTCTGGAGACTGGGGCAGGAGG GATGCCAGCTGGGAATAGTGGCGTATACCTGCGATCCCAGCTACTCTGGAGACTGGGGCAGGAGG A G UNK Ensembl:ENSG00000132478 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1055912677 Functional Loss SNV dbSNP153 33..33 33 - - - 42104 RMVar_ID_42104 Human_SNP_ID_632958406 A-to-I Human chr17 + 75807761 75807761 75807761 AGGCATGAGCCACCGTGCCCAGCCGTTTTTTTATATTTTTAGTAGAGACCGGGTTTCAGCAGTTT AGGCATGAGCCACCGTGCCCAGCCGTTTTTTTGTATTTTTAGTAGAGACCGGGTTTCAGCAGTTT A G UNK Ensembl:ENSG00000132478 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1316578271 Functional Loss SNV dbSNP153 33..33 33 - - - 42105 RMVar_ID_42105 Human_SNP_ID_632959129 A-to-I Human chr17 + 75810825 75810825 75810825 TACCCAGCTAATTTTGCATTTTTAGTAGAGACAGGGTTTCACCATGCTGACCAGGCTAGTCTCGA TACCCAGCTAATTTTGCATTTTTAGTAGAGACGGGGTTTCACCATGCTGACCAGGCTAGTCTCGA A G UNK Ensembl:ENSG00000132478 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1318186469 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51779 42106 RMVar_ID_42106 Human_SNP_ID_632967181 A-to-I Human chr17 - 75837158 75837158 75837158 GGGAGGCTGAGGCTGGAGAATCGCTTGAACCCAGGAGGCGCAGGTTGCAGTGAGCCGAGATCACG GGGAGGCTGAGGCTGGAGAATCGCTTGAACCCGGGAGGCGCAGGTTGCAGTGAGCCGAGATCACG T C UNC13D Ensembl:ENSG00000092929 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs570463311 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27770,RMVar_hsa_circ_85627,RMVar_hsa_circ_95033,RMVar_hsa_circ_112771,RMVar_hsa_circ_187107,RMVar_hsa_circ_187108,RMVar_hsa_circ_187106,RMVar_hsa_circ_104703,RMVar_hsa_circ_187109 42107 RMVar_ID_42107 Human_SNP_ID_632967290 A-to-I Human chr17 - 75837702 75837702 75837702 TCGCCCAGGCTGGAGTGCCATGGCACAATCTCAGCTCACTGCAACTTCTGCCTCCCAGGTTCAAG TCGCCCAGGCTGGAGTGCCATGGCACAATCTCGGCTCACTGCAACTTCTGCCTCCCAGGTTCAAG T C UNC13D Ensembl:ENSG00000092929 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1484279950 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27770,RMVar_hsa_circ_85627,RMVar_hsa_circ_95033,RMVar_hsa_circ_112771,RMVar_hsa_circ_187107,RMVar_hsa_circ_187108,RMVar_hsa_circ_187106,RMVar_hsa_circ_104703,RMVar_hsa_circ_187109 42108 RMVar_ID_42108 Human_SNP_ID_632967299 A-to-I Human chr17 - 75837747 75837747 75837747 TTCTTTTCTTTTCTTTTTTTTTTTTGAGCTGGAGTTTCCCTCTTGTCGCCCAGGCTGGAGTGCCA TTCTTTTCTTTTCTTTTTTTTTTTTGAGCTGGGGTTTCCCTCTTGTCGCCCAGGCTGGAGTGCCA T C UNC13D Ensembl:ENSG00000092929 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1177495697 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27770,RMVar_hsa_circ_85627,RMVar_hsa_circ_95033,RMVar_hsa_circ_112771,RMVar_hsa_circ_187107,RMVar_hsa_circ_187108,RMVar_hsa_circ_187106,RMVar_hsa_circ_104703,RMVar_hsa_circ_187109 42109 RMVar_ID_42109 Human_SNP_ID_632967603 A-to-I Human chr17 - 75838844 75838844 75838844 CGCCCGCCTTGGCCTCCCAAAGTGCTGGGATTATAGGCGCGTGCCACCGCGCCCAGCCTTTGCTG CGCCCGCCTTGGCCTCCCAAAGTGCTGGGATTTTAGGCGCGTGCCACCGCGCCCAGCCTTTGCTG T A UNC13D Ensembl:ENSG00000092929 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1021101402 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27770,RMVar_hsa_circ_85627,RMVar_hsa_circ_95033,RMVar_hsa_circ_112771,RMVar_hsa_circ_187107,RMVar_hsa_circ_187108,RMVar_hsa_circ_187106,RMVar_hsa_circ_104703,RMVar_hsa_circ_187109 42110 RMVar_ID_42110 Human_SNP_ID_632982745 A-to-I Human chr17 - 75889117 75889101 75889117 CAGGAGGTGAGGTTGCAGTGAGCTGAGATTGCACCACTGGACTACAGCCTGGGTGACAGAGCGAG CAGGAGGTGAGGTTGCAGTGAGCTGAGATTGC________________CTGGGTGACAGAGCGAG GGCTGTAGTCCAGTGGT G TRIM65 Ensembl:ENSG00000141569 Protein coding intron GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459,32596459 RNA-Seq:(High) rs775423973 Functional Loss DEL dbSNP153 33..48 33 - - - Human_RBP_ID_5144395,Human_RBP_ID_13165685,Human_RBP_ID_25325350,Human_RBP_ID_26455306 42111 RMVar_ID_42111 Human_SNP_ID_632982754 A-to-I Human chr17 - 75889148 75889148 75889148 GGGAGGCTGAGGCAGAAGAATCGCTTGAACCCAGGAGGTGAGGTTGCAGTGAGCTGAGATTGCAC GGGAGGCTGAGGCAGAAGAATCGCTTGAACCCCGGAGGTGAGGTTGCAGTGAGCTGAGATTGCAC T G TRIM65 Ensembl:ENSG00000141569 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348545074 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13165686,Human_RBP_ID_26459845 42112 RMVar_ID_42112 Human_SNP_ID_632982782 A-to-I Human chr17 - 75889238 75889238 75889238 CAGCCTGGCCAACAAGGCAAAACCCCGTCTCTACTAAAAATACAAAAATTAGCCGGGCATGGTGG CAGCCTGGCCAACAAGGCAAAACCCCGTCTCTGCTAAAAATACAAAAATTAGCCGGGCATGGTGG T C TRIM65 Ensembl:ENSG00000141569 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1470847329 Functional Loss SNV dbSNP153 33..33 33 - - - 42113 RMVar_ID_42113 Human_SNP_ID_632982815 A-to-I Human chr17 - 75889343 75889343 75889343 GGTTCCAAGGGTGTCTGCTTTTGGCCAGGCGCAGTGGCTCACGCTTGTAATCCCAGCACTTTGGG GGTTCCAAGGGTGTCTGCTTTTGGCCAGGCGCGGTGGCTCACGCTTGTAATCCCAGCACTTTGGG T C TRIM65 Ensembl:ENSG00000141569 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1243193994 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_500121,Human_RBP_ID_13165687,Human_RBP_ID_22059437,Human_RBP_ID_26458259 42114 RMVar_ID_42114 Human_SNP_ID_632982951 A-to-I Human chr17 - 75889858 75889858 75889858 GGGGTGCGGTCATGGGCTCATGGGATTCTCCTACCTCAGCCTCCTGAGTAGCTGGGATTACAGGT GGGGTGCGGTCATGGGCTCATGGGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGT T C TRIM65 Ensembl:ENSG00000141569 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,31158229,32596459,32596459 RNA-Seq:(High) rs887362650 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_500130,Human_RBP_ID_13165722,Human_RBP_ID_18708888,Human_RBP_ID_26458263 Human_miRNA_ID_1586,Human_miRNA_ID_5251,Human_miRNA_ID_8894,Human_miRNA_ID_12419,Human_miRNA_ID_16004,Human_miRNA_ID_19655,Human_miRNA_ID_23300,Human_miRNA_ID_26957,Human_miRNA_ID_491367,Human_miRNA_ID_494624,Human_miRNA_ID_1306283 42115 RMVar_ID_42115 Human_SNP_ID_632983020 A-to-I Human chr17 - 75890168 75890168 75890168 CTCTGTCACTCAGGCTGGAGTACAGTGGCACAATCATGGCTCACTGCAGCCTCGAGCTCCTGAGC CTCTGTCACTCAGGCTGGAGTACAGTGGCACAGTCATGGCTCACTGCAGCCTCGAGCTCCTGAGC T C TRIM65 Ensembl:ENSG00000141569 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs934121667 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_500137,Human_RBP_ID_22961651,Human_RBP_ID_24416614,Human_RBP_ID_26458267 42116 RMVar_ID_42116 Human_SNP_ID_632987191 A-to-I Human chr17 - 75902522 75902522 75902522 CGCCCCCTCACTGGGTGCAGTGGCTTGCGCCTATAATCCCAGCTACTTAGGAGGCTGAGGCAGGA CGCCCCCTCACTGGGTGCAGTGGCTTGCGCCTGTAATCCCAGCTACTTAGGAGGCTGAGGCAGGA T C MRPL38,AC087289.3 Ensembl:ENSG00000204316,Ensembl:ENSG00000267426 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1291791095 Functional Loss SNV dbSNP153 33..33 33 - - - 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_62723,RMVar_hsa_circ_104568,RMVar_hsa_circ_187120 42117 RMVar_ID_42117 Human_SNP_ID_632987369 A-to-I Human chr17 - 75903216 75903216 75903216 TTAGTAGAGATGGGGTTTCACCATATTGCCCAAGCTGGTCTGAAACTCCTGACCTCAAGTGATCC TTAGTAGAGATGGGGTTTCACCATATTGCCCAGGCTGGTCTGAAACTCCTGACCTCAAGTGATCC T C MRPL38,AC087289.3 Ensembl:ENSG00000204316,Ensembl:ENSG00000267426 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1034407538 Functional Loss SNV dbSNP153 33..33 33 - - - 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_62723,RMVar_hsa_circ_104568,RMVar_hsa_circ_187120 42118 RMVar_ID_42118 Human_SNP_ID_632995089 A-to-I Human chr17 - 75929129 75929129 75929129 GAAATCTTTCTCCTCAAAGGCCAGGCACCTGTAATCCCAGAACTTTGGGAGGCCGAGGCAGTAGG GAAATCTTTCTCCTCAAAGGCCAGGCACCTGTGATCCCAGAACTTTGGGAGGCCGAGGCAGTAGG T C AC087289.3,FBF1 Ensembl:ENSG00000267426,Ensembl:ENSG00000188878 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1058139 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22931,RMVar_hsa_circ_37015,RMVar_hsa_circ_15714,RMVar_hsa_circ_44297,RMVar_hsa_circ_42882 42119 RMVar_ID_42119 Human_SNP_ID_632998848 A-to-I Human chr17 - 75943046 75943046 75943046 AATTTTTGTATTTTGAGCAGAGATGGAGTTTCACCATGTTGGCCAGGTGATCTGCACTCCCACTC AATTTTTGTATTTTGAGCAGAGATGGAGTTTCGCCATGTTGGCCAGGTGATCTGCACTCCCACTC T C ACOX1 Ensembl:ENSG00000161533 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs950753898 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4451884,Human_RBP_ID_13166356,Human_RBP_ID_17494027 Human_Splice_Rec_1870094 42120 RMVar_ID_42120 Human_SNP_ID_632998862 A-to-I Human chr17 - 75943114 75943112 75943115 TCGAGCGATTCTCCCACCTCAGCCTCCTGAGTAGCTGGGATTACAGGCACCTGCCATCACGCTCG TCGAGCGATTCTCCCACCTCAGCCTCCTGAG___CTGGGATTACAGGCACCTGCCATCACGCTCG GCTA G ACOX1 Ensembl:ENSG00000161533 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1278404131 Functional Loss DEL dbSNP153 32..34 33 - - - Human_Splice_Rec_1870092 42121 RMVar_ID_42121 Human_SNP_ID_632998890 A-to-I Human chr17 - 75943188 75943188 75943188 TTTTGAGATGGAGTCTCCCAGGCGGGAATGCAATGGTGCGATCTCGACTTCACTGCAATCTTCAC TTTTGAGATGGAGTCTCCCAGGCGGGAATGCAGTGGTGCGATCTCGACTTCACTGCAATCTTCAC T C ACOX1 Ensembl:ENSG00000161533 Protein coding 3'UTR GSE38233;GSE107867 cultured B-cells;ASD brains,frontal_cortex - 24183664,30559470 RNA-Seq:(High) rs1217815791 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18708947,Human_RBP_ID_24481099 Human_Splice_Rec_1870092 42122 RMVar_ID_42122 Human_SNP_ID_632998961 A-to-I Human chr17 - 75943414 75943414 75943414 CCTGCTTTGGCCTCCTCTGAGAAGCTGGGATTACTGGTGCACACCACCACACCTGGCTAATTTTT CCTGCTTTGGCCTCCTCTGAGAAGCTGGGATTTCTGGTGCACACCACCACACCTGGCTAATTTTT T A ACOX1 Ensembl:ENSG00000161533 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs768776823 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1870093 42123 RMVar_ID_42123 Human_SNP_ID_632999071 A-to-I Human chr17 - 75944014 75944014 75944014 GTTGCCCAGGCTGGTCTCAGACTCCTGGGCTCAAGCGATCATTTCGCCTCAGCCTCCCAAAGTGC GTTGCCCAGGCTGGTCTCAGACTCCTGGGCTCGAGCGATCATTTCGCCTCAGCCTCCCAAAGTGC T C ACOX1 Ensembl:ENSG00000161533 Protein coding 3'UTR GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs899157082 Functional Loss SNV dbSNP153 33..33 33 - - - 42124 RMVar_ID_42124 Human_SNP_ID_632999096 A-to-I Human chr17 - 75944134 75944134 75944134 TGCCTCCCGGGTTCAAATGGTCCTCCCTCCTCAGTCTCCTGAGTAGCTGGGACGACAGGCACGTG TGCCTCCCGGGTTCAAATGGTCCTCCCTCCTCGGTCTCCTGAGTAGCTGGGACGACAGGCACGTG T C ACOX1 Ensembl:ENSG00000161533 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs548386840 Functional Loss SNV dbSNP153 33..33 33 - - - 42125 RMVar_ID_42125 Human_SNP_ID_632999116 A-to-I Human chr17 - 75944226 75944225 75944227 GAGTAGGAATTTTATTTTTATCTTTTTGAGACAGGGTATCACTGTCACCCAGACTGGAGTGCAGT GAGTAGGAATTTTATTTTTATCTTTTTGAGA__GGGTATCACTGTCACCCAGACTGGAGTGCAGT CTG C ACOX1 Ensembl:ENSG00000161533 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1219611585 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_26455340 42126 RMVar_ID_42126 Human_SNP_ID_632999117 A-to-I Human chr17 - 75944226 75944226 75944226 GAGTAGGAATTTTATTTTTATCTTTTTGAGACAGGGTATCACTGTCACCCAGACTGGAGTGCAGT GAGTAGGAATTTTATTTTTATCTTTTTGAGACTGGGTATCACTGTCACCCAGACTGGAGTGCAGT T A ACOX1 Ensembl:ENSG00000161533 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs112325564 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26455340 42127 RMVar_ID_42127 Human_SNP_ID_632999118 A-to-I Human chr17 - 75944226 75944226 75944226 GAGTAGGAATTTTATTTTTATCTTTTTGAGACAGGGTATCACTGTCACCCAGACTGGAGTGCAGT GAGTAGGAATTTTATTTTTATCTTTTTGAGACGGGGTATCACTGTCACCCAGACTGGAGTGCAGT T C ACOX1 Ensembl:ENSG00000161533 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs112325564 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26455340 42128 RMVar_ID_42128 Human_SNP_ID_632999120 A-to-I Human chr17 - 75944230 75944230 75944230 TACTGAGTAGGAATTTTATTTTTATCTTTTTGAGACAGGGTATCACTGTCACCCAGACTGGAGTG TACTGAGTAGGAATTTTATTTTTATCTTTTTGGGACAGGGTATCACTGTCACCCAGACTGGAGTG T C ACOX1 Ensembl:ENSG00000161533 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1293920409 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26455340 42129 RMVar_ID_42129 Human_SNP_ID_632999148 A-to-I Human chr17 - 75944359 75944348 75944359 TGGCAAGTCCAGTTTGTTCTCTCTACCACACTAGACTGCCACTGACAAGTTTGGGTCTGTTGGAT TGGCAAGTCCAGTTTGTTCTCTCTACCACACT___________GACAAGTTTGGGTCTGTTGGAT CAGTGGCAGTCT C ACOX1 Ensembl:ENSG00000161533 Protein coding 3'UTR GSE38233;GSE100210;GSE107867;GSE107867;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;ASD brains,cerebellum;ASD brains,temporal_cortex;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,30559470,30559470,32596459 RNA-Seq:(High) rs1394612222 Functional Loss DEL dbSNP153 33..43 33 - - - Human_RBP_ID_6644572,Human_RBP_ID_27669583 42130 RMVar_ID_42130 Human_SNP_ID_632999244 A-to-I Human chr17 - 75944855 75944855 75944855 CGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGATAATCGCTTGAACTTGGCGGGTAGA CGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGGGGCAGGATAATCGCTTGAACTTGGCGGGTAGA T C ACOX1 Ensembl:ENSG00000161533 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs563277377 Functional Loss SNV dbSNP153 33..33 33 - - - 42131 RMVar_ID_42131 Human_SNP_ID_632999257 A-to-I Human chr17 - 75944899 75944899 75944899 TCTACTGAAAAAAATACAAAAATTAGCTGGGCATGGTGGTAGCACGCGCCTGTAGTCCCAGCTAC TCTACTGAAAAAAATACAAAAATTAGCTGGGCGTGGTGGTAGCACGCGCCTGTAGTCCCAGCTAC T C ACOX1 Ensembl:ENSG00000161533 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1325631258 Functional Loss SNV dbSNP153 33..33 33 - - - 42132 RMVar_ID_42132 Human_SNP_ID_632999258 A-to-I Human chr17 - 75944899 75944899 75944899 TCTACTGAAAAAAATACAAAAATTAGCTGGGCATGGTGGTAGCACGCGCCTGTAGTCCCAGCTAC TCTACTGAAAAAAATACAAAAATTAGCTGGGCCTGGTGGTAGCACGCGCCTGTAGTCCCAGCTAC T G ACOX1 Ensembl:ENSG00000161533 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1325631258 Functional Loss SNV dbSNP153 33..33 33 - - - 42133 RMVar_ID_42133 Human_SNP_ID_632999274 A-to-I Human chr17 - 75944983 75944983 75944983 CAAGCACTTTGGGAGGCCGAAGCGGGTGGATCACCTGAGGTCAGGAGTTTGAGACCATCCTGGCC CAAGCACTTTGGGAGGCCGAAGCGGGTGGATCGCCTGAGGTCAGGAGTTTGAGACCATCCTGGCC T C ACOX1 Ensembl:ENSG00000161533 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1292268716 Functional Loss SNV dbSNP153 33..33 33 - - - 42134 RMVar_ID_42134 Human_SNP_ID_632999283 A-to-I Human chr17 - 75945019 75945019 75945019 ATCTGGGGCCAGGCGTGGTGGCTCACGCCTGTAATCCAAGCACTTTGGGAGGCCGAAGCGGGTGG ATCTGGGGCCAGGCGTGGTGGCTCACGCCTGTGATCCAAGCACTTTGGGAGGCCGAAGCGGGTGG T C ACOX1 Ensembl:ENSG00000161533 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1422296499 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17566192,Human_RBP_ID_26455343 42135 RMVar_ID_42135 Human_SNP_ID_633009435 A-to-I Human chr17 + 75980202 75980202 75980202 CTACAAAAAATACCAAAAAATTAGCTGGGTGTAGTGGCATGCGCCTGTAGTCCCAGCTACTCTGA CTACAAAAAATACCAAAAAATTAGCTGGGTGTGGTGGCATGCGCCTGTAGTCCCAGCTACTCTGA A G TEN1,TEN1-CDK3 Ensembl:ENSG00000257949,Ensembl:ENSG00000261408 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1333182305 Functional Loss SNV dbSNP153 33..33 33 - - - 42136 RMVar_ID_42136 Human_SNP_ID_633027850 A-to-I Human chr17 - 76041995 76041995 76041995 CCTGTGGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCGTGAACGCGGGAGGCGGAGCTT CCTGTGGTCCCAGCTACTCGGGAGGCTGAGGCTGGAGAATGGCGTGAACGCGGGAGGCGGAGCTT T A SRP68 Ensembl:ENSG00000167881 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs946821317 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_131699 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 42137 RMVar_ID_42137 Human_SNP_ID_633027976 A-to-I Human chr17 - 76042469 76042469 76042469 GTGGCACGATCTCGGCTTGTGCCACCAAGCCCAGCTAATTTTTGTATTTTTAGTAGAGGGTTTCA GTGGCACGATCTCGGCTTGTGCCACCAAGCCCCGCTAATTTTTGTATTTTTAGTAGAGGGTTTCA T G SRP68 Ensembl:ENSG00000167881 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985341958 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22221342 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 42138 RMVar_ID_42138 Human_SNP_ID_633027986 A-to-I Human chr17 - 76042509 76042509 76042509 TTTTTTAAGATGGAGTCTCTGTCTCCTAGGCTAGAGTGCAGTGGCACGATCTCGGCTTGTGCCAC TTTTTTAAGATGGAGTCTCTGTCTCCTAGGCTGGAGTGCAGTGGCACGATCTCGGCTTGTGCCAC T C SRP68 Ensembl:ENSG00000167881 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs961563645 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22586916 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 42139 RMVar_ID_42139 Human_SNP_ID_633028053 A-to-I Human chr17 - 76042840 76042840 76042840 TGGCTCATGCCTGTAATCCCAGCAGTTTGGGAAGCTGAGGTGGGCAGATCACTTGAGGTAAGGAG TGGCTCATGCCTGTAATCCCAGCAGTTTGGGATGCTGAGGTGGGCAGATCACTTGAGGTAAGGAG T A SRP68 Ensembl:ENSG00000167881 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1233685428 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42140 RMVar_ID_42140 Human_SNP_ID_633028092 A-to-I Human chr17 - 76043029 76043029 76043029 GAACTCATGGCCTCGAACTCCTGGCCTCAAGCAGTCCTCCTGCCTCTGCCTCCCAAAACCTTGAG GAACTCATGGCCTCGAACTCCTGGCCTCAAGCGGTCCTCCTGCCTCTGCCTCCCAAAACCTTGAG T C SRP68 Ensembl:ENSG00000167881 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs768968699 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17566586 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 42141 RMVar_ID_42141 Human_SNP_ID_633028101 A-to-I Human chr17 - 76043099 76043087 76043099 CCACCATACCAGGCCAATTTTTATTTTTTTGTAGAGATGGGGGTCTCACTATGTTGCCCAGGCTG CCACCATACCAGGCCAATTTTTATTTTTTTGT____________CTCACTATGTTGCCCAGGCTG GACCCCCATCTCT G SRP68 Ensembl:ENSG00000167881 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs1341265460 Functional Loss DEL dbSNP153 33..44 33 - - - 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 42142 RMVar_ID_42142 Human_SNP_ID_633028134 A-to-I Human chr17 - 76043223 76043223 76043223 TCTCGCTCTGTCACCCAGGCTGGAATGCAAGTAGCACCATCATAGTTCACTGCAGCCTCGAACTC TCTCGCTCTGTCACCCAGGCTGGAATGCAAGTGGCACCATCATAGTTCACTGCAGCCTCGAACTC T C SRP68 Ensembl:ENSG00000167881 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1272269063 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20270141 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 42143 RMVar_ID_42143 Human_SNP_ID_633030877 A-to-I Human chr17 - 76054626 76054626 76054626 GTAGGTCTCGAACTCCTGACTTCAGGCAATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTAC GTAGGTCTCGAACTCCTGACTTCAGGCAATCCCCCCGCCTCGGCCTCCCAAAGTGCTGGGATTAC T G SRP68 Ensembl:ENSG00000167881 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924672820 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42144 RMVar_ID_42144 Human_SNP_ID_633030880 A-to-I Human chr17 - 76054630 76054630 76054630 TTTAGTAGGTCTCGAACTCCTGACTTCAGGCAATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGA TTTAGTAGGTCTCGAACTCCTGACTTCAGGCAGTCCACCCGCCTCGGCCTCCCAAAGTGCTGGGA T C SRP68 Ensembl:ENSG00000167881 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs369544638 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42145 RMVar_ID_42145 Human_SNP_ID_633031135 A-to-I Human chr17 - 76055632 76055632 76055632 CTCCTGCCTCAGCCTCCAGAGTAGCTGGGACTACAGGCACCCACCATCACACCCGGCTAATTTTT CTCCTGCCTCAGCCTCCAGAGTAGCTGGGACTGCAGGCACCCACCATCACACCCGGCTAATTTTT T C SRP68 Ensembl:ENSG00000167881 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1199049297 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42146 RMVar_ID_42146 Human_SNP_ID_633032071 A-to-I Human chr17 - 76059522 76059522 76059522 TATTTATTTATTTAGAGTCGGAGTCTTGCTCTATCGCCAGGCTGGAGTGCAATGGTGCAATCTTG TATTTATTTATTTAGAGTCGGAGTCTTGCTCTGTCGCCAGGCTGGAGTGCAATGGTGCAATCTTG T C SRP68 Ensembl:ENSG00000167881 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1010585603 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6644796,Human_RBP_ID_13167232 RMVar_hsa_circ_10493,RMVar_hsa_circ_34247,RMVar_hsa_circ_108311,RMVar_hsa_circ_187155,RMVar_hsa_circ_351379,RMVar_hsa_circ_112529,RMVar_hsa_circ_187157,RMVar_hsa_circ_59036,RMVar_hsa_circ_187159,RMVar_hsa_circ_354689,RMVar_hsa_circ_369297,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 42147 RMVar_ID_42147 Human_SNP_ID_633032811 A-to-I Human chr17 - 76062102 76062102 76062102 TTTTGTATTTTTAGTAGAGACAGGTTTTCACCATGTTGGCCAGGCTGGTCCCCAACTCCTGACCT TTTTGTATTTTTAGTAGAGACAGGTTTTCACCGTGTTGGCCAGGCTGGTCCCCAACTCCTGACCT T C SRP68 Ensembl:ENSG00000167881 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs541130443 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108311,RMVar_hsa_circ_187155,RMVar_hsa_circ_351379,RMVar_hsa_circ_112529,RMVar_hsa_circ_187157,RMVar_hsa_circ_59036,RMVar_hsa_circ_354689,RMVar_hsa_circ_308428,RMVar_hsa_circ_341208,RMVar_hsa_circ_326868,RMVar_hsa_circ_32583,RMVar_hsa_circ_187161,RMVar_hsa_circ_360351,RMVar_hsa_circ_378378,RMVar_hsa_circ_187163,RMVar_hsa_circ_52667 42148 RMVar_ID_42148 Human_SNP_ID_633033585 A-to-I Human chr17 - 76063043 76063043 76063043 TTCTTAGGCCGGGCGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGCAG TTCTTAGGCCGGGCGTGGTGGCTCACGCCTGTCATCCCAGCACTTTGGGAGGCCAAGGTGGGCAG T G SRP68 Ensembl:ENSG00000167881 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs959625011 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108311,RMVar_hsa_circ_187155,RMVar_hsa_circ_351379,RMVar_hsa_circ_112529,RMVar_hsa_circ_187157,RMVar_hsa_circ_59036,RMVar_hsa_circ_354689,RMVar_hsa_circ_308428,RMVar_hsa_circ_341208,RMVar_hsa_circ_326868,RMVar_hsa_circ_32583,RMVar_hsa_circ_187161,RMVar_hsa_circ_360351,RMVar_hsa_circ_378378,RMVar_hsa_circ_187163,RMVar_hsa_circ_52667 42149 RMVar_ID_42149 Human_SNP_ID_633034791 A-to-I Human chr17 - 76067588 76067588 76067588 TGGTGGTACACCTCTGTTGGTCACATCTACCCAGGAGGCTGAGGTGGGAGGATTGACTGAGCCTG TGGTGGTACACCTCTGTTGGTCACATCTACCCCGGAGGCTGAGGTGGGAGGATTGACTGAGCCTG T G SRP68 Ensembl:ENSG00000167881 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1438677858 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108311,RMVar_hsa_circ_187155,RMVar_hsa_circ_351379,RMVar_hsa_circ_112529,RMVar_hsa_circ_187157,RMVar_hsa_circ_59036,RMVar_hsa_circ_326868,RMVar_hsa_circ_32583,RMVar_hsa_circ_325379,RMVar_hsa_circ_187166,RMVar_hsa_circ_296705,RMVar_hsa_circ_187167 42150 RMVar_ID_42150 Human_SNP_ID_633034812 A-to-I Human chr17 - 76067664 76067664 76067664 TCCAAGGATTTCGAGACCAGCCTGGGTGACATAGTGAAACCCTGTCTCTACAAAAAGTACAAAAA TCCAAGGATTTCGAGACCAGCCTGGGTGACATGGTGAAACCCTGTCTCTACAAAAAGTACAAAAA T C SRP68 Ensembl:ENSG00000167881 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946045627 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108311,RMVar_hsa_circ_187155,RMVar_hsa_circ_351379,RMVar_hsa_circ_112529,RMVar_hsa_circ_187157,RMVar_hsa_circ_59036,RMVar_hsa_circ_326868,RMVar_hsa_circ_32583,RMVar_hsa_circ_325379,RMVar_hsa_circ_187166,RMVar_hsa_circ_296705,RMVar_hsa_circ_187167 42151 RMVar_ID_42151 Human_SNP_ID_633099908 A-to-I Human chr17 - 76298946 76298946 76298946 ATTTCAGGACAGACTGTAAAGAAAGTTTGAAAAGCTACAAAAGCAAATAAAAACTACACTCAGGG ATTTCAGGACAGACTGTAAAGAAAGTTTGAAACGCTACAAAAGCAAATAAAAACTACACTCAGGG T G QRICH2 Ensembl:ENSG00000129646 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1330066104 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6645083 RMVar_hsa_circ_97290,RMVar_hsa_circ_82253,RMVar_hsa_circ_105710,RMVar_hsa_circ_187186,RMVar_hsa_circ_49539,RMVar_hsa_circ_187188,RMVar_hsa_circ_78838,RMVar_hsa_circ_187190,RMVar_hsa_circ_86772,RMVar_hsa_circ_187191,RMVar_hsa_circ_187197,RMVar_hsa_circ_301383,RMVar_hsa_circ_187192,RMVar_hsa_circ_278695,RMVar_hsa_circ_187196 42152 RMVar_ID_42152 Human_SNP_ID_633100395 A-to-I Human chr17 - 76300972 76300972 76300972 TTGGCTCACTGCAACCTCCACCTCCCGAGCTCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGC TTGGCTCACTGCAACCTCCACCTCCCGAGCTCGAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGC T C QRICH2 Ensembl:ENSG00000129646 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs866282419 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97290,RMVar_hsa_circ_82253,RMVar_hsa_circ_105710,RMVar_hsa_circ_187186,RMVar_hsa_circ_49539,RMVar_hsa_circ_187188,RMVar_hsa_circ_78838,RMVar_hsa_circ_187190,RMVar_hsa_circ_86772,RMVar_hsa_circ_187191,RMVar_hsa_circ_187197,RMVar_hsa_circ_301383,RMVar_hsa_circ_187192,RMVar_hsa_circ_278695,RMVar_hsa_circ_187196 42153 RMVar_ID_42153 Human_SNP_ID_633100396 A-to-I Human chr17 - 76300972 76300972 76300972 TTGGCTCACTGCAACCTCCACCTCCCGAGCTCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGC TTGGCTCACTGCAACCTCCACCTCCCGAGCTCCAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGC T G QRICH2 Ensembl:ENSG00000129646 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs866282419 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97290,RMVar_hsa_circ_82253,RMVar_hsa_circ_105710,RMVar_hsa_circ_187186,RMVar_hsa_circ_49539,RMVar_hsa_circ_187188,RMVar_hsa_circ_78838,RMVar_hsa_circ_187190,RMVar_hsa_circ_86772,RMVar_hsa_circ_187191,RMVar_hsa_circ_187197,RMVar_hsa_circ_301383,RMVar_hsa_circ_187192,RMVar_hsa_circ_278695,RMVar_hsa_circ_187196 42154 RMVar_ID_42154 Human_SNP_ID_633101652 A-to-I Human chr17 - 76305385 76305385 76305385 GAGGCTGGAGGATTGCTCGGACCCAGGAGTTCAAGACCAGCCTGGGCAACATTGCAAGATCTTAT GAGGCTGGAGGATTGCTCGGACCCAGGAGTTCCAGACCAGCCTGGGCAACATTGCAAGATCTTAT T G QRICH2 Ensembl:ENSG00000129646 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs887876030 Functional Loss SNV dbSNP153 33..33 33 - - - 42155 RMVar_ID_42155 Human_SNP_ID_633101794 A-to-I Human chr17 - 76306054 76306054 76306054 GGAATTCTCCTGCCTCGGCTTCCCGAGTAGCTAGGATTATAGGTGCACACCACCATGCCCAGCTA GGAATTCTCCTGCCTCGGCTTCCCGAGTAGCTGGGATTATAGGTGCACACCACCATGCCCAGCTA T C QRICH2 Ensembl:ENSG00000129646 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1450461491 Functional Loss SNV dbSNP153 33..33 33 - - - 42156 RMVar_ID_42156 Human_SNP_ID_633108708 A-to-I Human chr17 - 76329538 76329538 76329538 TAGAGATGGGGTTTCACCATGTTCATCAGACTAGTCTTGAACTCCTGACCTCAAGTGATCTGTCT TAGAGATGGGGTTTCACCATGTTCATCAGACTGGTCTTGAACTCCTGACCTCAAGTGATCTGTCT T C PRPSAP1 Ensembl:ENSG00000161542 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1263323157 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41561,RMVar_hsa_circ_10759,RMVar_hsa_circ_78070,RMVar_hsa_circ_187200,RMVar_hsa_circ_187204,RMVar_hsa_circ_327042,RMVar_hsa_circ_312983 42157 RMVar_ID_42157 Human_SNP_ID_633112667 A-to-I Human chr17 - 76344061 76344061 76344061 CATGCGCCTGTAGTCCAGCTGTTTGAGAGGCTAAGGCAGGAGAAGTGCTTGAACCCAGGAGGCAG CATGCGCCTGTAGTCCAGCTGTTTGAGAGGCTGAGGCAGGAGAAGTGCTTGAACCCAGGAGGCAG T C PRPSAP1 Ensembl:ENSG00000161542 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1422596169 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_595,RMVar_hsa_circ_312983 42158 RMVar_ID_42158 Human_SNP_ID_633127157 A-to-I Human chr17 - 76392473 76392473 76392473 ATCACTTGAGCCCAGGAGTTCGAGACCAACCTAGGCAACATAGTGAAACCCTGTCTGTACACAAA ATCACTTGAGCCCAGGAGTTCGAGACCAACCTGGGCAACATAGTGAAACCCTGTCTGTACACAAA T C UBE2O Ensembl:ENSG00000175931 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1171926775 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_187207,RMVar_hsa_circ_86497,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_187214,RMVar_hsa_circ_187212,RMVar_hsa_circ_187209,RMVar_hsa_circ_187210,RMVar_hsa_circ_187208,RMVar_hsa_circ_118189,RMVar_hsa_circ_187206,RMVar_hsa_circ_187217,RMVar_hsa_circ_12448 42159 RMVar_ID_42159 Human_SNP_ID_633127171 A-to-I Human chr17 - 76392546 76392546 76392546 TTCCAGGCAAGGGCCAGGCACAGTGACGGCTCAGGGCTGTAAACCCAGCACTTTGGGAGGCCGAG TTCCAGGCAAGGGCCAGGCACAGTGACGGCTCGGGGCTGTAAACCCAGCACTTTGGGAGGCCGAG T C UBE2O Ensembl:ENSG00000175931 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs533640058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13169065 RMVar_hsa_circ_187207,RMVar_hsa_circ_86497,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_187214,RMVar_hsa_circ_187212,RMVar_hsa_circ_187209,RMVar_hsa_circ_187210,RMVar_hsa_circ_187208,RMVar_hsa_circ_118189,RMVar_hsa_circ_187206,RMVar_hsa_circ_187217,RMVar_hsa_circ_12448 42160 RMVar_ID_42160 Human_SNP_ID_633127233 A-to-I Human chr17 - 76392735 76392735 76392735 TTGGCCAGACTGCTCTTGAACTCCTGACCTTAAGTGATCCACCCGTCTCGGCCTCCCAAAGTGCT TTGGCCAGACTGCTCTTGAACTCCTGACCTTAGGTGATCCACCCGTCTCGGCCTCCCAAAGTGCT T C UBE2O Ensembl:ENSG00000175931 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs538224945 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13169071 RMVar_hsa_circ_187207,RMVar_hsa_circ_86497,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_187214,RMVar_hsa_circ_187212,RMVar_hsa_circ_187209,RMVar_hsa_circ_187210,RMVar_hsa_circ_187208,RMVar_hsa_circ_118189,RMVar_hsa_circ_187206,RMVar_hsa_circ_187217,RMVar_hsa_circ_12448 42161 RMVar_ID_42161 Human_SNP_ID_633127240 A-to-I Human chr17 - 76392761 76392761 76392761 TTTAGTAGAGACGGGGTTTCACCACGTTGGCCAGACTGCTCTTGAACTCCTGACCTTAAGTGATC TTTAGTAGAGACGGGGTTTCACCACGTTGGCCCGACTGCTCTTGAACTCCTGACCTTAAGTGATC T G UBE2O Ensembl:ENSG00000175931 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1177407997 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_187207,RMVar_hsa_circ_86497,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_187214,RMVar_hsa_circ_187212,RMVar_hsa_circ_187209,RMVar_hsa_circ_187210,RMVar_hsa_circ_187208,RMVar_hsa_circ_118189,RMVar_hsa_circ_187206,RMVar_hsa_circ_187217,RMVar_hsa_circ_12448 42162 RMVar_ID_42162 Human_SNP_ID_633127277 A-to-I Human chr17 - 76392867 76392867 76392867 GCTCACTGCAACCTCCGCCTCCGGGTTGAAGCAATTCTCCCACCTCAGCCTCCCGAGTAGCTGGG GCTCACTGCAACCTCCGCCTCCGGGTTGAAGCGATTCTCCCACCTCAGCCTCCCGAGTAGCTGGG T C UBE2O Ensembl:ENSG00000175931 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs371463239 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18709247,Human_RBP_ID_25326308 RMVar_hsa_circ_187207,RMVar_hsa_circ_86497,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_187214,RMVar_hsa_circ_187212,RMVar_hsa_circ_187209,RMVar_hsa_circ_187210,RMVar_hsa_circ_187208,RMVar_hsa_circ_118189,RMVar_hsa_circ_187206,RMVar_hsa_circ_187217,RMVar_hsa_circ_12448 42163 RMVar_ID_42163 Human_SNP_ID_633127289 A-to-I Human chr17 - 76392913 76392913 76392913 TAGCGTCGCACTGTCACCCAGGCTAGAGTTCAATGGCACAATCTCGGCTCACTGCAACCTCCGCC TAGCGTCGCACTGTCACCCAGGCTAGAGTTCAGTGGCACAATCTCGGCTCACTGCAACCTCCGCC T C UBE2O Ensembl:ENSG00000175931 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1017887459 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13169072,Human_RBP_ID_23308612 RMVar_hsa_circ_187207,RMVar_hsa_circ_86497,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_187214,RMVar_hsa_circ_187212,RMVar_hsa_circ_187209,RMVar_hsa_circ_187210,RMVar_hsa_circ_187208,RMVar_hsa_circ_118189,RMVar_hsa_circ_187206,RMVar_hsa_circ_187217,RMVar_hsa_circ_12448 42164 RMVar_ID_42164 Human_SNP_ID_633127318 A-to-I Human chr17 - 76393001 76393001 76393001 TCCCACCTTGGCCTCCCAAAAGTGCTGGGATTACAGGTGTGAGCCATCACGTCTGGCTGAGGAAT TCCCACCTTGGCCTCCCAAAAGTGCTGGGATTTCAGGTGTGAGCCATCACGTCTGGCTGAGGAAT T A UBE2O Ensembl:ENSG00000175931 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1023714081 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_187207,RMVar_hsa_circ_86497,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_187214,RMVar_hsa_circ_187212,RMVar_hsa_circ_187209,RMVar_hsa_circ_187210,RMVar_hsa_circ_187208,RMVar_hsa_circ_118189,RMVar_hsa_circ_187206,RMVar_hsa_circ_187217,RMVar_hsa_circ_12448 42165 RMVar_ID_42165 Human_SNP_ID_633127342 A-to-I Human chr17 - 76393076 76393076 76393076 TTTTTTATTTTTTGTAGAGATAGGGTCCCACTATGTTGCCCAGGTTGGTTTTGACCTCCTGGCCT TTTTTTATTTTTTGTAGAGATAGGGTCCCACTGTGTTGCCCAGGTTGGTTTTGACCTCCTGGCCT T C UBE2O Ensembl:ENSG00000175931 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1392824005 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25326312,Human_RBP_ID_27457337 RMVar_hsa_circ_187207,RMVar_hsa_circ_86497,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_187214,RMVar_hsa_circ_187212,RMVar_hsa_circ_187209,RMVar_hsa_circ_187210,RMVar_hsa_circ_187208,RMVar_hsa_circ_118189,RMVar_hsa_circ_187206,RMVar_hsa_circ_187217,RMVar_hsa_circ_12448 42166 RMVar_ID_42166 Human_SNP_ID_633152447 A-to-I Human chr17 - 76482452 76482452 76482452 TTATCTTTGAAAAATGAACTGGGGCTGGGCACAGTGAGCTTGCACCTGTAATCCCAGCACTTGGG TTATCTTTGAAAAATGAACTGGGGCTGGGCACGGTGAGCTTGCACCTGTAATCCCAGCACTTGGG T C RHBDF2 Ensembl:ENSG00000129667 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1349425432 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_306022 42167 RMVar_ID_42167 Human_SNP_ID_633153109 A-to-I Human chr17 - 76484809 76484809 76484809 CTCCATTGCTTTTGATCATGAACCCCACCCCCAGCAGAGCTTGGCCAGTTTGAGACAATGAGGGG CTCCATTGCTTTTGATCATGAACCCCACCCCCGGCAGAGCTTGGCCAGTTTGAGACAATGAGGGG T C RHBDF2 Ensembl:ENSG00000129667 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4238990 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_306022 42168 RMVar_ID_42168 Human_SNP_ID_633153244 A-to-I Human chr17 - 76485311 76485311 76485311 CACCTTCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGGATGCA CACCTTCCAGGTTCAAGCGATTCTCCTGCCTCGGCCTCCCGAGTAGCTGGGATTACAGGGATGCA T C RHBDF2 Ensembl:ENSG00000129667 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs954738582 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_306022 42169 RMVar_ID_42169 Human_SNP_ID_633174242 A-to-I Human chr17 + 76559239 76559238 76559240 AAAGAGCATTTTTTGTTTGTTTGTTTTGAGACAGAGTTTTGCTCTTGTTGCCCAGGCTGGAGTGC AAAGAGCATTTTTTGTTTGTTTGTTTTGAGAC__AGTTTTGCTCTTGTTGCCCAGGCTGGAGTGC CAG C SNHG16 Ensembl:ENSG00000163597 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs199576189 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_6659313 RMVar_hsa_circ_29973,RMVar_hsa_circ_110530,RMVar_hsa_circ_187228,RMVar_hsa_circ_97345,RMVar_hsa_circ_187232 42170 RMVar_ID_42170 Human_SNP_ID_633174409 A-to-I Human chr17 + 76559825 76559825 76559825 CCTGGCCAACATGGTGAAACCTTGTCTCTACTAAAAATACAAAAATTAGCTGGGTGTGGTGGCGG CCTGGCCAACATGGTGAAACCTTGTCTCTACTGAAAATACAAAAATTAGCTGGGTGTGGTGGCGG A G SNHG16 Ensembl:ENSG00000163597 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1014978225 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29973,RMVar_hsa_circ_110530,RMVar_hsa_circ_187228,RMVar_hsa_circ_97345,RMVar_hsa_circ_187232 42171 RMVar_ID_42171 Human_SNP_ID_633174419 A-to-I Human chr17 + 76559888 76559888 76559888 GGGCACCTGTAATCCTAGCTACTTGGGAGACTAAGGCAGGAGAATCTCTTGAACCCAGGAGGCAG GGGCACCTGTAATCCTAGCTACTTGGGAGACTCAGGCAGGAGAATCTCTTGAACCCAGGAGGCAG A C SNHG16 Ensembl:ENSG00000163597 lincRNA intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1202573335 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8254967 RMVar_hsa_circ_29973,RMVar_hsa_circ_110530,RMVar_hsa_circ_187228,RMVar_hsa_circ_97345,RMVar_hsa_circ_187232 42172 RMVar_ID_42172 Human_SNP_ID_633174420 A-to-I Human chr17 + 76559893 76559893 76559893 CCTGTAATCCTAGCTACTTGGGAGACTAAGGCAGGAGAATCTCTTGAACCCAGGAGGCAGAGGTT CCTGTAATCCTAGCTACTTGGGAGACTAAGGCGGGAGAATCTCTTGAACCCAGGAGGCAGAGGTT A G SNHG16 Ensembl:ENSG00000163597 lincRNA intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs778325660 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8254967,Human_RBP_ID_13170730 RMVar_hsa_circ_29973,RMVar_hsa_circ_110530,RMVar_hsa_circ_187228,RMVar_hsa_circ_97345,RMVar_hsa_circ_187232 42173 RMVar_ID_42173 Human_SNP_ID_633174421 A-to-I Human chr17 + 76559893 76559893 76559893 CCTGTAATCCTAGCTACTTGGGAGACTAAGGCAGGAGAATCTCTTGAACCCAGGAGGCAGAGGTT CCTGTAATCCTAGCTACTTGGGAGACTAAGGCTGGAGAATCTCTTGAACCCAGGAGGCAGAGGTT A T SNHG16 Ensembl:ENSG00000163597 lincRNA intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs778325660 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8254967,Human_RBP_ID_13170730 RMVar_hsa_circ_29973,RMVar_hsa_circ_110530,RMVar_hsa_circ_187228,RMVar_hsa_circ_97345,RMVar_hsa_circ_187232 42174 RMVar_ID_42174 Human_SNP_ID_633175855 A-to-I Human chr17 - 76564454 76564453 76564455 CAGCCAGGGTAACAAATTGAGACCCCCCCCCAACTTTAAAATTAAAAAACGAAAGAAAAAATAGC CAGCCAGGGTAACAAATTGAGACCCCCCCCC__CTTTAAAATTAAAAAACGAAAGAAAAAATAGC GTT G AC015802.6 Ensembl:ENSG00000284526 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1491356654 Functional Loss DEL dbSNP153 32..33 33 - - - 42175 RMVar_ID_42175 Human_SNP_ID_633175856 A-to-I Human chr17 - 76564454 76564453 76564454 CAGCCAGGGTAACAAATTGAGACCCCCCCCCAACTTTAAAATTAAAAAACGAAAGAAAAAATAGC CAGCCAGGGTAACAAATTGAGACCCCCCCCCA_CTTTAAAATTAAAAAACGAAAGAAAAAATAGC GT G AC015802.6 Ensembl:ENSG00000284526 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1555627184 Functional Loss DEL dbSNP153 33..33 33 - - - 42176 RMVar_ID_42176 Human_SNP_ID_633176018 A-to-I Human chr17 - 76564878 76564878 76564878 GGACAGCAGGAATTAAGAGAGATTTCAGAGTTACTGGCACGAGGACAAAGCCTCTCAGCTCGCTT GGACAGCAGGAATTAAGAGAGATTTCAGAGTTGCTGGCACGAGGACAAAGCCTCTCAGCTCGCTT T C AC015802.6 Ensembl:ENSG00000284526 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs553255966 Functional Loss SNV dbSNP153 33..33 33 - - - 42177 RMVar_ID_42177 Human_SNP_ID_633176019 A-to-I Human chr17 - 76564878 76564878 76564878 GGACAGCAGGAATTAAGAGAGATTTCAGAGTTACTGGCACGAGGACAAAGCCTCTCAGCTCGCTT GGACAGCAGGAATTAAGAGAGATTTCAGAGTTCCTGGCACGAGGACAAAGCCTCTCAGCTCGCTT T G AC015802.6 Ensembl:ENSG00000284526 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs553255966 Functional Loss SNV dbSNP153 33..33 33 - - - 42178 RMVar_ID_42178 Human_SNP_ID_633179826 A-to-I Human chr17 - 76577710 76577710 76577710 AAATTAGGCAGGCATGGTGGCGGGCTCCTGTAATCCCAGCTACTTGGGAGACTGAGGCAGAATTG AAATTAGGCAGGCATGGTGGCGGGCTCCTGTAGTCCCAGCTACTTGGGAGACTGAGGCAGAATTG T C ST6GALNAC2 Ensembl:ENSG00000070731 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1245503868 Functional Loss SNV dbSNP153 33..33 33 - - - 42179 RMVar_ID_42179 Human_SNP_ID_633180194 A-to-I Human chr17 - 76579120 76579120 76579120 GAAGTCGGGAGTTCGAGACCAGCCTGACCAACATGGAAAAACCCCGTCTCTACTAAAAATACAAA GAAGTCGGGAGTTCGAGACCAGCCTGACCAACGTGGAAAAACCCCGTCTCTACTAAAAATACAAA T C ST6GALNAC2 Ensembl:ENSG00000070731 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1308613050 Functional Loss SNV dbSNP153 33..33 33 - - - 42180 RMVar_ID_42180 Human_SNP_ID_633180195 A-to-I Human chr17 - 76579122 76579121 76579122 CTGAAGTCGGGAGTTCGAGACCAGCCTGACCAACATGGAAAAACCCCGTCTCTACTAAAAATACA CTGAAGTCGGGAGTTCGAGACCAGCCTGACCA_CATGGAAAAACCCCGTCTCTACTAAAAATACA GT G ST6GALNAC2 Ensembl:ENSG00000070731 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1205109578 Functional Loss DEL dbSNP153 33..33 33 - - - 42181 RMVar_ID_42181 Human_SNP_ID_633195888 A-to-I Human chr17 + 76631153 76631153 76631153 GTGTTTAGAGACTGGATCTCACTCTGTTACCCAGGCTGGTCTCAAATTCCTCACCTCAAGTGATC GTGTTTAGAGACTGGATCTCACTCTGTTACCCTGGCTGGTCTCAAATTCCTCACCTCAAGTGATC A T SNHG16 RNACentral:URS0000D5A137 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1047101258 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13172834 42182 RMVar_ID_42182 Human_SNP_ID_633206786 A-to-I Human chr17 - 76675559 76675559 76675559 AAAACCCTGTCTCTACTACAAATACAAAAATTAGCCAGGCGTGGTAGCGCACGCCTGTAATCCCA AAAACCCTGTCTCTACTACAAATACAAAAATTGGCCAGGCGTGGTAGCGCACGCCTGTAATCCCA T C MXRA7 Ensembl:ENSG00000182534 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs531532847 Functional Loss SNV dbSNP153 33..33 33 - - - 42183 RMVar_ID_42183 Human_SNP_ID_633210421 A-to-I Human chr17 - 76689175 76689175 76689175 TGAGGCAGGAGAATCGCTTAAACCCAGGAGGCAGACGTTGCAGTGAGCCGAGATCGCGCCACTGC TGAGGCAGGAGAATCGCTTAAACCCAGGAGGCGGACGTTGCAGTGAGCCGAGATCGCGCCACTGC T C MXRA7 Ensembl:ENSG00000182534 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs536099527 Functional Loss SNV dbSNP153 33..33 33 - - - 42184 RMVar_ID_42184 Human_SNP_ID_633210452 A-to-I Human chr17 - 76689281 76689281 76689281 CGAGACCAGCCCGGCCAACATGGTGACATGCCATCTCTACTGAAAACACAAAAAAATTAGCTGGG CGAGACCAGCCCGGCCAACATGGTGACATGCCTTCTCTACTGAAAACACAAAAAAATTAGCTGGG T A MXRA7 Ensembl:ENSG00000182534 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459047376 Functional Loss SNV dbSNP153 33..33 33 - - - 42185 RMVar_ID_42185 Human_SNP_ID_633210581 A-to-I Human chr17 - 76689781 76689781 76689781 GCTGGTCTCGAATTCCCAACCTCAGCTGATCCACCCACCTAGGCCTCCCAAAATTCTGGGATTAC GCTGGTCTCGAATTCCCAACCTCAGCTGATCCGCCCACCTAGGCCTCCCAAAATTCTGGGATTAC T C MXRA7 Ensembl:ENSG00000182534 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs761397778 Functional Loss SNV dbSNP153 33..33 33 - - - 42186 RMVar_ID_42186 Human_SNP_ID_633210599 A-to-I Human chr17 - 76689841 76689841 76689841 ACACTCGGCTAATTTTTTTTTGTATTTTTAGTAGAGACGGGGTTTTGCCATGTTGGCCAGGCTGG ACACTCGGCTAATTTTTTTTTGTATTTTTAGTGGAGACGGGGTTTTGCCATGTTGGCCAGGCTGG T C MXRA7 Ensembl:ENSG00000182534 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1225622831 Functional Loss SNV dbSNP153 33..33 33 - - - 42187 RMVar_ID_42187 Human_SNP_ID_633210602 A-to-I Human chr17 - 76689850 76689850 76689850 CCTGCCACAACACTCGGCTAATTTTTTTTTGTATTTTTAGTAGAGACGGGGTTTTGCCATGTTGG CCTGCCACAACACTCGGCTAATTTTTTTTTGTTTTTTTAGTAGAGACGGGGTTTTGCCATGTTGG T A MXRA7 Ensembl:ENSG00000182534 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1231767688 Functional Loss SNV dbSNP153 33..33 33 - - - 42188 RMVar_ID_42188 Human_SNP_ID_633210873 A-to-I Human chr17 - 76690831 76690831 76690831 TGGTGGCATGCACCTGTGATCCCAGCTATTCCAGAGGCTGAGGCAGGAGGATCGCTTGAGCCCTG TGGTGGCATGCACCTGTGATCCCAGCTATTCCGGAGGCTGAGGCAGGAGGATCGCTTGAGCCCTG T C MXRA7 Ensembl:ENSG00000182534 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1168680687 Functional Loss SNV dbSNP153 33..33 33 - - - 42189 RMVar_ID_42189 Human_SNP_ID_633212986 A-to-I Human chr17 - 76698753 76698753 76698753 CCACCATTGCATCCCAGCCTGGGCAACAGAGCAAGACTCTTATCTCAAAAAAAAAAAAAAAAAAA CCACCATTGCATCCCAGCCTGGGCAACAGAGCGAGACTCTTATCTCAAAAAAAAAAAAAAAAAAA T C MXRA7 Ensembl:ENSG00000182534 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1162984253 Functional Loss SNV dbSNP153 33..33 33 - - - 42190 RMVar_ID_42190 Human_SNP_ID_633214020 A-to-I Human chr17 - 76702776 76702776 76702776 GCGATCTTGGCTCACTGCAACCTACCCCTCCCAGGTTCCAGCGATTCTCTTGCCTCAGGCTCCCA GCGATCTTGGCTCACTGCAACCTACCCCTCCCGGGTTCCAGCGATTCTCTTGCCTCAGGCTCCCA T C MXRA7 Ensembl:ENSG00000182534 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs967380679 Functional Loss SNV dbSNP153 33..33 33 - - - 42191 RMVar_ID_42191 Human_SNP_ID_633218175 A-to-I Human chr17 - 76717334 76717334 76717334 AGTAAAATACTGAAGTTGAAGCTAGGCATCGTAGCTCAAGCCTGTAATCCCAGCACTTTGGGAGG AGTAAAATACTGAAGTTGAAGCTAGGCATCGTGGCTCAAGCCTGTAATCCCAGCACTTTGGGAGG T C JMJD6 Ensembl:ENSG00000070495 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991476897 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23750810 42192 RMVar_ID_42192 Human_SNP_ID_633218382 A-to-I Human chr17 - 76717922 76717922 76717922 CAGTGATGCGATCTCGGCTTATTGTAACCTCTACCTCCCAGGTTCAAGCAATTTTCCTGCCTCAG CAGTGATGCGATCTCGGCTTATTGTAACCTCTGCCTCCCAGGTTCAAGCAATTTTCCTGCCTCAG T C JMJD6 Ensembl:ENSG00000070495 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1253225430 Functional Loss SNV dbSNP153 33..33 33 - - - 42193 RMVar_ID_42193 Human_SNP_ID_633218859 A-to-I Human chr17 - 76719453 76719453 76719453 GAAATCCCATGTCTACTAAAAACACAAAAATTAGTTGGGTGTGGTGGTGCACACCTGTAATCCCA GAAATCCCATGTCTACTAAAAACACAAAAATTGGTTGGGTGTGGTGGTGCACACCTGTAATCCCA T C JMJD6 Ensembl:ENSG00000070495 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1369811152 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55438,RMVar_hsa_circ_364309,RMVar_hsa_circ_187242 42194 RMVar_ID_42194 Human_SNP_ID_633219767 A-to-I Human chr17 - 76722663 76722663 76722663 TTTTTGTATTTTAGTAGAGACGGGGTTTCATCATGTTGCCCAGGCTGGTCTTGAACTCTTGAGCT TTTTTGTATTTTAGTAGAGACGGGGTTTCATCGTGTTGCCCAGGCTGGTCTTGAACTCTTGAGCT T C JMJD6 Ensembl:ENSG00000070495 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941543652 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55438,RMVar_hsa_circ_363283,RMVar_hsa_circ_56844 42195 RMVar_ID_42195 Human_SNP_ID_633219768 A-to-I Human chr17 - 76722663 76722663 76722663 TTTTTGTATTTTAGTAGAGACGGGGTTTCATCATGTTGCCCAGGCTGGTCTTGAACTCTTGAGCT TTTTTGTATTTTAGTAGAGACGGGGTTTCATCCTGTTGCCCAGGCTGGTCTTGAACTCTTGAGCT T G JMJD6 Ensembl:ENSG00000070495 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941543652 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55438,RMVar_hsa_circ_363283,RMVar_hsa_circ_56844 42196 RMVar_ID_42196 Human_SNP_ID_633219797 A-to-I Human chr17 - 76722737 76722737 76722737 GGTTCAAGCGATTCTCTTGTCTCAGCCTCCCAAGTAGCTGGGAATACAGGCACATGCCGCCACAC GGTTCAAGCGATTCTCTTGTCTCAGCCTCCCAGGTAGCTGGGAATACAGGCACATGCCGCCACAC T C JMJD6 Ensembl:ENSG00000070495 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs559264907 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55438,RMVar_hsa_circ_363283,RMVar_hsa_circ_56844 42197 RMVar_ID_42197 Human_SNP_ID_633219806 A-to-I Human chr17 - 76722763 76722763 76722763 CAGCCCACTACAACCTCCTCCTCCCAGGTTCAAGCGATTCTCTTGTCTCAGCCTCCCAAGTAGCT CAGCCCACTACAACCTCCTCCTCCCAGGTTCAGGCGATTCTCTTGTCTCAGCCTCCCAAGTAGCT T C JMJD6 Ensembl:ENSG00000070495 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1567999562 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55438,RMVar_hsa_circ_363283,RMVar_hsa_circ_56844 42198 RMVar_ID_42198 Human_SNP_ID_633219949 A-to-I Human chr17 - 76723070 76723070 76723070 GTGGTGGCGGGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAATCCG GTGGTGGCGGGCGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAATCCG T C JMJD6 Ensembl:ENSG00000070495 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1197838797 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55438,RMVar_hsa_circ_363283,RMVar_hsa_circ_56844 42199 RMVar_ID_42199 Human_SNP_ID_633220369 A-to-I Human chr17 - 76724259 76724259 76724259 AAATTAGCCAGGCGTGGTGGTGTGCGTCGGTAATCCCAGCTACTCAGGAGGCTAAGGCAGGAGAA AAATTAGCCAGGCGTGGTGGTGTGCGTCGGTAGTCCCAGCTACTCAGGAGGCTAAGGCAGGAGAA T C JMJD6 Ensembl:ENSG00000070495 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1311643147 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55438,RMVar_hsa_circ_363283,RMVar_hsa_circ_56844 42200 RMVar_ID_42200 Human_SNP_ID_633221688 A-to-I Human chr17 + 76727401 76727399 76727402 GGAGACCCTGCCAAGAAGTGACCCTGGTCACTATGTTGGTCAGGCTGGTCTCGAACTGTAAGCTT GGAGACCCTGCCAAGAAGTGACCCTGGTCAC___GTTGGTCAGGCTGGTCTCGAACTGTAAGCTT CTAT C METTL23 Ensembl:ENSG00000181038 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1479182961 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_26758430,Human_RBP_ID_27260243 42201 RMVar_ID_42201 Human_SNP_ID_633221696 A-to-I Human chr17 + 76727434 76727433 76727435 TGTTGGTCAGGCTGGTCTCGAACTGTAAGCTTAAGTGATCCTCCTGCCTCGGCCTCCCAAAGTGC TGTTGGTCAGGCTGGTCTCGAACTGTAAGCTT__GTGATCCTCCTGCCTCGGCCTCCCAAAGTGC TAA T METTL23 Ensembl:ENSG00000181038 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1239116977 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_1542994,Human_RBP_ID_13174819,Human_RBP_ID_18709509,Human_RBP_ID_26758952 42202 RMVar_ID_42202 Human_SNP_ID_633221706 A-to-I Human chr17 + 76727460 76727460 76727460 AAGCTTAAGTGATCCTCCTGCCTCGGCCTCCCAAAGTGCTAGGATTACAGGCATGAGCCACTGCG AAGCTTAAGTGATCCTCCTGCCTCGGCCTCCCGAAGTGCTAGGATTACAGGCATGAGCCACTGCG A G METTL23 Ensembl:ENSG00000181038 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985507885 Functional Loss SNV dbSNP153 33..33 33 - - - 42203 RMVar_ID_42203 Human_SNP_ID_633221879 A-to-I Human chr17 + 76728093 76728093 76728093 GATACTACGTCTCTACAAAAAGTAGAAAAATTAGGCATCGTGGCTTGTGCCTGTAGCCCCAGCTA GATACTACGTCTCTACAAAAAGTAGAAAAATTGGGCATCGTGGCTTGTGCCTGTAGCCCCAGCTA A G METTL23 Ensembl:ENSG00000181038 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1185066121 Functional Loss SNV dbSNP153 33..33 33 - - - 42204 RMVar_ID_42204 Human_SNP_ID_633221951 A-to-I Human chr17 + 76728310 76728307 76728311 ATTGTTTCCAAACAGCTTCACTTTTTTTTGCTAACTGCAACCTCAACCTCTGGGCTCAAGTGATC ATTGTTTCCAAACAGCTTCACTTTTTTTTG____CTGCAACCTCAACCTCTGGGCTCAAGTGATC GCTAA G METTL23 Ensembl:ENSG00000181038 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1326227678 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_13174838 42205 RMVar_ID_42205 Human_SNP_ID_633222189 A-to-I Human chr17 + 76729006 76729006 76729006 TTAGTGGAGTAGAGACGGGGTTTCACCGCGTTAGCCAGGATGGTCTCGATCTCCTGACCTGATGA TTAGTGGAGTAGAGACGGGGTTTCACCGCGTTGGCCAGGATGGTCTCGATCTCCTGACCTGATGA A G METTL23 Ensembl:ENSG00000181038 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs549776021 Functional Loss SNV dbSNP153 33..33 33 - - - 42206 RMVar_ID_42206 Human_SNP_ID_633228726 A-to-I Human chr17 + 76749454 76749454 76749454 GAGAGACTGAGGTGGGAGAATCGCTTACGCCCAGGACGCGGAGGTTGCAGTGAGCCAAGATAATC GAGAGACTGAGGTGGGAGAATCGCTTACGCCCGGGACGCGGAGGTTGCAGTGAGCCAAGATAATC A G MFSD11 Ensembl:ENSG00000092931 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs996075101 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58117,RMVar_hsa_circ_360692,RMVar_hsa_circ_358927,RMVar_hsa_circ_277760,RMVar_hsa_circ_187252,RMVar_hsa_circ_187253,RMVar_hsa_circ_367506,RMVar_hsa_circ_43955,RMVar_hsa_circ_10712,RMVar_hsa_circ_320575,RMVar_hsa_circ_187255,RMVar_hsa_circ_324791,RMVar_hsa_circ_75085,RMVar_hsa_circ_187257,RMVar_hsa_circ_187258,RMVar_hsa_circ_6710,RMVar_hsa_circ_326453,RMVar_hsa_circ_309291,RMVar_hsa_circ_187259,RMVar_hsa_circ_187260,RMVar_hsa_circ_61958,RMVar_hsa_circ_30270,RMVar_hsa_circ_91997,RMVar_hsa_circ_187262 42207 RMVar_ID_42207 Human_SNP_ID_633229273 A-to-I Human chr17 + 76751444 76751444 76751444 GGATGGGTGTGGTGGTTCACACCTGTAATCCCAACACTTTGGGAGGCTGAAGTCAGAGGATCACT GGATGGGTGTGGTGGTTCACACCTGTAATCCCGACACTTTGGGAGGCTGAAGTCAGAGGATCACT A G MFSD11 Ensembl:ENSG00000092931 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1358945632 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58117,RMVar_hsa_circ_360692,RMVar_hsa_circ_358927,RMVar_hsa_circ_277760,RMVar_hsa_circ_187252,RMVar_hsa_circ_187253,RMVar_hsa_circ_367506,RMVar_hsa_circ_43955,RMVar_hsa_circ_10712,RMVar_hsa_circ_320575,RMVar_hsa_circ_187255,RMVar_hsa_circ_324791,RMVar_hsa_circ_75085,RMVar_hsa_circ_187257,RMVar_hsa_circ_187258,RMVar_hsa_circ_6710,RMVar_hsa_circ_326453,RMVar_hsa_circ_309291,RMVar_hsa_circ_187259,RMVar_hsa_circ_187260,RMVar_hsa_circ_61958,RMVar_hsa_circ_30270,RMVar_hsa_circ_91997,RMVar_hsa_circ_187262 42208 RMVar_ID_42208 Human_SNP_ID_633229548 A-to-I Human chr17 + 76752590 76752590 76752590 TTTAGTAGAGATAGGGTTTCGCCATGTTGGCCAGGCTGATCTGAAACTCCTGACCTCAAGTAATC TTTAGTAGAGATAGGGTTTCGCCATGTTGGCCGGGCTGATCTGAAACTCCTGACCTCAAGTAATC A G MFSD11 Ensembl:ENSG00000092931 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1358679901 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58117,RMVar_hsa_circ_360692,RMVar_hsa_circ_358927,RMVar_hsa_circ_277760,RMVar_hsa_circ_187252,RMVar_hsa_circ_187253,RMVar_hsa_circ_367506,RMVar_hsa_circ_43955,RMVar_hsa_circ_10712,RMVar_hsa_circ_320575,RMVar_hsa_circ_187255,RMVar_hsa_circ_324791,RMVar_hsa_circ_75085,RMVar_hsa_circ_187257,RMVar_hsa_circ_187258,RMVar_hsa_circ_6710,RMVar_hsa_circ_326453,RMVar_hsa_circ_309291,RMVar_hsa_circ_187259,RMVar_hsa_circ_187260,RMVar_hsa_circ_61958,RMVar_hsa_circ_30270,RMVar_hsa_circ_91997,RMVar_hsa_circ_187262 42209 RMVar_ID_42209 Human_SNP_ID_633231192 A-to-I Human chr17 + 76758418 76758418 76758418 TAGTCTGGGCAACATGATGCACCTCTCTCTCTACAAAAGGTACAAAAATTAGCTGGGTTTTGGGG TAGTCTGGGCAACATGATGCACCTCTCTCTCTCCAAAAGGTACAAAAATTAGCTGGGTTTTGGGG A C MFSD11 Ensembl:ENSG00000092931 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1487233439 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58117,RMVar_hsa_circ_360692,RMVar_hsa_circ_277760,RMVar_hsa_circ_187252,RMVar_hsa_circ_187253,RMVar_hsa_circ_367506,RMVar_hsa_circ_43955,RMVar_hsa_circ_10712,RMVar_hsa_circ_320575,RMVar_hsa_circ_187255,RMVar_hsa_circ_324791,RMVar_hsa_circ_75085,RMVar_hsa_circ_187257,RMVar_hsa_circ_187258,RMVar_hsa_circ_6710,RMVar_hsa_circ_326453,RMVar_hsa_circ_309291,RMVar_hsa_circ_187259,RMVar_hsa_circ_187260,RMVar_hsa_circ_61958,RMVar_hsa_circ_91997,RMVar_hsa_circ_187262,RMVar_hsa_circ_316360,RMVar_hsa_circ_326028,RMVar_hsa_circ_187263 42210 RMVar_ID_42210 Human_SNP_ID_633231641 A-to-I Human chr17 + 76759849 76759849 76759849 GTTGGCCAGACTGGTTTTGAACTCCTGACCTCAAGTGATCCACCCACCCGGCCTCCCAAAGTGCT GTTGGCCAGACTGGTTTTGAACTCCTGACCTCTAGTGATCCACCCACCCGGCCTCCCAAAGTGCT A T MFSD11 Ensembl:ENSG00000092931 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs538502794 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22717536,Human_RBP_ID_25327091 RMVar_hsa_circ_58117,RMVar_hsa_circ_360692,RMVar_hsa_circ_277760,RMVar_hsa_circ_187252,RMVar_hsa_circ_187253,RMVar_hsa_circ_367506,RMVar_hsa_circ_43955,RMVar_hsa_circ_10712,RMVar_hsa_circ_320575,RMVar_hsa_circ_187255,RMVar_hsa_circ_324791,RMVar_hsa_circ_75085,RMVar_hsa_circ_187257,RMVar_hsa_circ_187258,RMVar_hsa_circ_6710,RMVar_hsa_circ_326453,RMVar_hsa_circ_309291,RMVar_hsa_circ_187259,RMVar_hsa_circ_187260,RMVar_hsa_circ_61958,RMVar_hsa_circ_91997,RMVar_hsa_circ_187262,RMVar_hsa_circ_316360,RMVar_hsa_circ_326028,RMVar_hsa_circ_187263 42211 RMVar_ID_42211 Human_SNP_ID_633231872 A-to-I Human chr17 + 76760648 76760648 76760648 CACCTCTTGGGTTCAAGGGATTCTCCTGCCTCAGGCTCCTGAGTAGCTGGGATTACAGGTGAATG CACCTCTTGGGTTCAAGGGATTCTCCTGCCTCGGGCTCCTGAGTAGCTGGGATTACAGGTGAATG A G MFSD11 Ensembl:ENSG00000092931 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1302261333 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58117,RMVar_hsa_circ_360692,RMVar_hsa_circ_277760,RMVar_hsa_circ_187252,RMVar_hsa_circ_187253,RMVar_hsa_circ_367506,RMVar_hsa_circ_43955,RMVar_hsa_circ_10712,RMVar_hsa_circ_320575,RMVar_hsa_circ_187255,RMVar_hsa_circ_324791,RMVar_hsa_circ_75085,RMVar_hsa_circ_187257,RMVar_hsa_circ_187258,RMVar_hsa_circ_6710,RMVar_hsa_circ_326453,RMVar_hsa_circ_309291,RMVar_hsa_circ_187259,RMVar_hsa_circ_187260,RMVar_hsa_circ_61958,RMVar_hsa_circ_91997,RMVar_hsa_circ_187262,RMVar_hsa_circ_316360,RMVar_hsa_circ_326028,RMVar_hsa_circ_187263 42212 RMVar_ID_42212 Human_SNP_ID_633235972 A-to-I Human chr17 + 76777006 76777006 76777006 TTTAAAGACAAAGTCGGCCCGCCGCGGCTCACACTTGTAATCCCAGCACTTTGGGAGGCCAAGGT TTTAAAGACAAAGTCGGCCCGCCGCGGCTCACGCTTGTAATCCCAGCACTTTGGGAGGCCAAGGT A G MFSD11 Ensembl:ENSG00000092931 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs550670741 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_187253,RMVar_hsa_circ_187267 42213 RMVar_ID_42213 Human_SNP_ID_633236087 A-to-I Human chr17 + 76777327 76777327 76777327 TCACTCTGTAGTCCAGACTGGAGTGCAGTGGCACGATCTTGGCTCAGTGCAATCTCTGCCTCCCA TCACTCTGTAGTCCAGACTGGAGTGCAGTGGCGCGATCTTGGCTCAGTGCAATCTCTGCCTCCCA A G MFSD11 Ensembl:ENSG00000092931 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170413424 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_187253,RMVar_hsa_circ_187267 42214 RMVar_ID_42214 Human_SNP_ID_633236467 A-to-I Human chr17 + 76778835 76778835 76778835 AATAGCAAAGCTGGGTGTGGTGTTGCACCGCTATACTCCCAGCTGTTGGGGAGGCTGAGACAGAA AATAGCAAAGCTGGGTGTGGTGTTGCACCGCTGTACTCCCAGCTGTTGGGGAGGCTGAGACAGAA A G MFSD11 Ensembl:ENSG00000092931 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1255377677 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1869771 RMVar_hsa_circ_187253,RMVar_hsa_circ_187267 42215 RMVar_ID_42215 Human_SNP_ID_633236513 A-to-I Human chr17 + 76779043 76779043 76779043 GGGAGGCTGAGGTGGGTGGATCACCTGAGGTCAGGAGTTTGAGACCAGCCTGGCCAACATGGTGA GGGAGGCTGAGGTGGGTGGATCACCTGAGGTCGGGAGTTTGAGACCAGCCTGGCCAACATGGTGA A G MFSD11 Ensembl:ENSG00000092931 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1034633739 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_187253,RMVar_hsa_circ_187267 42216 RMVar_ID_42216 Human_SNP_ID_633236524 A-to-I Human chr17 + 76779138 76779138 76779138 TGTTGGGTTTGGTGGTGCATGCCTGTAATCCTAGCTACTAGGGAGGCTGAGGTAAGAGAATTCGC TGTTGGGTTTGGTGGTGCATGCCTGTAATCCTGGCTACTAGGGAGGCTGAGGTAAGAGAATTCGC A G MFSD11 Ensembl:ENSG00000092931 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs189890848 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_187253,RMVar_hsa_circ_187267 42217 RMVar_ID_42217 Human_SNP_ID_633236526 A-to-I Human chr17 + 76779142 76779142 76779142 GGGTTTGGTGGTGCATGCCTGTAATCCTAGCTACTAGGGAGGCTGAGGTAAGAGAATTCGCTTGA GGGTTTGGTGGTGCATGCCTGTAATCCTAGCTGCTAGGGAGGCTGAGGTAAGAGAATTCGCTTGA A G MFSD11 Ensembl:ENSG00000092931 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1568124344 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_187253,RMVar_hsa_circ_187267 42218 RMVar_ID_42218 Human_SNP_ID_633236936 A-to-I Human chr17 + 76780696 76780696 76780696 CACCACCCCGCCTGGCTAATTTTTGTATTTTCAGTAGAGACGGGGTTTCACCATGTTGGTCAGGC CACCACCCCGCCTGGCTAATTTTTGTATTTTCGGTAGAGACGGGGTTTCACCATGTTGGTCAGGC A G MFSD11 Ensembl:ENSG00000092931 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs549659196 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_187253,RMVar_hsa_circ_187267 42219 RMVar_ID_42219 Human_SNP_ID_633237197 A-to-I Human chr17 + 76781896 76781896 76781896 CAGGCTGGATCACAGTGGCACAGTCATGGCTCACTGCAGCTTTGACGTCTTGGGCTCAAGCAATA CAGGCTGGATCACAGTGGCACAGTCATGGCTCTCTGCAGCTTTGACGTCTTGGGCTCAAGCAATA A T SNHG16 RNACentral:URS0000D5A137 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909221096 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13175854 42220 RMVar_ID_42220 Human_SNP_ID_633238762 A-to-I Human chr17 + 76788038 76788037 76788039 TGTTTGTTTGTTTGTGGTTTTTTTTTTGAGACAGAGTCTCACTCTGTCACCCTGGGTGGAGTGAA TGTTTGTTTGTTTGTGGTTTTTTTTTTGAGAC__AGTCTCACTCTGTCACCCTGGGTGGAGTGAA CAG C SNHG16 RNACentral:URS0000D5A137 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1357319613 Functional Loss DEL dbSNP153 33..34 33 - - - 42221 RMVar_ID_42221 Human_SNP_ID_633238795 A-to-I Human chr17 + 76788206 76788206 76788206 GGATTTACAGTTGCACGCTGCCACACCTGGCTAATTTTTTGTATTTTTAGTAGAGACAGGGTGTT GGATTTACAGTTGCACGCTGCCACACCTGGCTGATTTTTTGTATTTTTAGTAGAGACAGGGTGTT A G SNHG16 RNACentral:URS0000D5A137 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1039613407 Functional Loss SNV dbSNP153 33..33 33 - - - 42222 RMVar_ID_42222 Human_SNP_ID_633238832 A-to-I Human chr17 + 76788389 76788388 76788390 TATATTTTGTTGTTTTGTTGTTGTTTTGAGACAGAGTCTCGCTGTGTTATCCAAGCTGGAGTGCA TATATTTTGTTGTTTTGTTGTTGTTTTGAGAC__AGTCTCGCTGTGTTATCCAAGCTGGAGTGCA CAG C SNHG16 RNACentral:URS0000D5A137 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1166941901 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_3538044 42223 RMVar_ID_42223 Human_SNP_ID_633320073 A-to-I Human chr17 + 77090169 77090169 77090169 TGGCCAACATGAAATTAGCTGGGTGCAGTGGCATATGCCTGTAATCCCAAGAGGCTGAGGCAGGA TGGCCAACATGAAATTAGCTGGGTGCAGTGGCGTATGCCTGTAATCCCAAGAGGCTGAGGCAGGA A G SNHG20,SEC14L1 Ensembl:ENSG00000234912,Ensembl:ENSG00000129657 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs915198150 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8255326 RMVar_hsa_circ_351125,RMVar_hsa_circ_187278 42224 RMVar_ID_42224 Human_SNP_ID_633320156 A-to-I Human chr17 + 77090421 77090421 77090421 TCACACCTGTAATCTGAGCACTTTGGGGTGCCAAGGTGGGAGGATCACTTGAGCTCAGGAGTTCG TCACACCTGTAATCTGAGCACTTTGGGGTGCCGAGGTGGGAGGATCACTTGAGCTCAGGAGTTCG A G SNHG20,SEC14L1 Ensembl:ENSG00000234912,Ensembl:ENSG00000129657 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1344336218 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1131934,Human_RBP_ID_3548942,Human_RBP_ID_5248036,Human_RBP_ID_6647050 RMVar_hsa_circ_351125,RMVar_hsa_circ_187278 42225 RMVar_ID_42225 Human_SNP_ID_633320523 A-to-I Human chr17 + 77091834 77091834 77091834 ACAGTTTATGAAATTTTTTTTTTTTTTTTGAGAAGGAGTCTTATTCTGTTGCCCAGGCTGAGTGC ACAGTTTATGAAATTTTTTTTTTTTTTTTGAGGAGGAGTCTTATTCTGTTGCCCAGGCTGAGTGC A G SNHG20,SEC14L1 Ensembl:ENSG00000234912,Ensembl:ENSG00000129657 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1406064790 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13176605,Human_RBP_ID_17567188 RMVar_hsa_circ_351125,RMVar_hsa_circ_187278 42226 RMVar_ID_42226 Human_SNP_ID_633320562 A-to-I Human chr17 + 77091977 77091977 77091977 GGGATTACAGGCACATGCCATCACACCCGGCTAATTTTTGTGTTTTTAGTAGAGACGGGGTTTCG GGGATTACAGGCACATGCCATCACACCCGGCTTATTTTTGTGTTTTTAGTAGAGACGGGGTTTCG A T SNHG20,SEC14L1 Ensembl:ENSG00000234912,Ensembl:ENSG00000129657 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs995836880 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_351125,RMVar_hsa_circ_187278 42227 RMVar_ID_42227 Human_SNP_ID_633321101 A-to-I Human chr17 + 77094087 77094087 77094087 GTTTTTGAGACAGAGTTTCGCTCTTGTGGCCCAGGCTGGAGTGCGGTGGTGTGACCTCGGCTCAC GTTTTTGAGACAGAGTTTCGCTCTTGTGGCCCGGGCTGGAGTGCGGTGGTGTGACCTCGGCTCAC A G SNHG20,SEC14L1 Ensembl:ENSG00000234912,Ensembl:ENSG00000129657 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs555206561 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_500990,Human_RBP_ID_766919,Human_RBP_ID_6647099,Human_RBP_ID_13176709,Human_RBP_ID_23751149 Human_Splice_Rec_1872988,Human_Splice_Rec_1872992 42228 RMVar_ID_42228 Human_SNP_ID_633323682 A-to-I Human chr17 + 77103511 77103511 77103511 CACCCCAGGCTGGAGGGCAGTGGTGTCATCTCAGCTCACTGCAACCTCTGCCTCCTGGGCTCAAG CACCCCAGGCTGGAGGGCAGTGGTGTCATCTCGGCTCACTGCAACCTCTGCCTCCTGGGCTCAAG A G SEC14L1 Ensembl:ENSG00000129657 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs111970036 Functional Loss SNV dbSNP153 33..33 33 - - - 42229 RMVar_ID_42229 Human_SNP_ID_633324005 A-to-I Human chr17 + 77104534 77104534 77104534 ATGTTTTTGGCCTGGTGTGGTGGCTCACGCCTATAATCCTAGCACTTTGGGAGGCCGAGGAGGGT ATGTTTTTGGCCTGGTGTGGTGGCTCACGCCTGTAATCCTAGCACTTTGGGAGGCCGAGGAGGGT A G SEC14L1 Ensembl:ENSG00000129657 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1249131962 Functional Loss SNV dbSNP153 33..33 33 - - - 42230 RMVar_ID_42230 Human_SNP_ID_633339161 A-to-I Human chr17 - 77161964 77161964 77161964 CCCTCACTGCGATCTATTGAAAGTCAGCCCTCAACACAAGGGTTTGTTTAAAAAAAAAAAAAGAA CCCTCACTGCGATCTATTGAAAGTCAGCCCTCGACACAAGGGTTTGTTTAAAAAAAAAAAAAGAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs796082512 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_269867,Human_RBP_ID_1289131,Human_RBP_ID_5275138,Human_RBP_ID_8464230,Human_RBP_ID_23308624,Human_RBP_ID_26461014 42231 RMVar_ID_42231 Human_SNP_ID_633339162 A-to-I Human chr17 - 77161964 77161964 77161964 CCCTCACTGCGATCTATTGAAAGTCAGCCCTCAACACAAGGGTTTGTTTAAAAAAAAAAAAAGAA CCCTCACTGCGATCTATTGAAAGTCAGCCCTCCACACAAGGGTTTGTTTAAAAAAAAAAAAAGAA T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs796082512 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_269867,Human_RBP_ID_1289131,Human_RBP_ID_5275138,Human_RBP_ID_8464230,Human_RBP_ID_23308624,Human_RBP_ID_26461014 42232 RMVar_ID_42232 Human_SNP_ID_633350217 A-to-I Human chr17 + 77202781 77202781 77202781 GTCTCTAGTAAAATACAAAAAATTAGCCGGGCATGGCAGCGTGCGCCTGTAGTTCCAGCTACTTG GTCTCTAGTAAAATACAAAAAATTAGCCGGGCGTGGCAGCGTGCGCCTGTAGTTCCAGCTACTTG A G SEC14L1 Ensembl:ENSG00000129657 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs8080207 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_4951,GWAS_ID_4952,GWAS_ID_4953,GWAS_ID_4954,GWAS_ID_4955,GWAS_ID_4956 RMVar_hsa_circ_98284,RMVar_hsa_circ_118861,RMVar_hsa_circ_187286,RMVar_hsa_circ_97983,RMVar_hsa_circ_187287,RMVar_hsa_circ_187285 42233 RMVar_ID_42233 Human_SNP_ID_633350234 A-to-I Human chr17 + 77202826 77202826 77202826 CCTGTAGTTCCAGCTACTTGGGAGGCTGAGGCAGGAGAATTGCTTGAACCTGCAGGCAGAGGTTG CCTGTAGTTCCAGCTACTTGGGAGGCTGAGGCTGGAGAATTGCTTGAACCTGCAGGCAGAGGTTG A T SEC14L1 Ensembl:ENSG00000129657 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1359777376 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98284,RMVar_hsa_circ_118861,RMVar_hsa_circ_187286,RMVar_hsa_circ_97983,RMVar_hsa_circ_187287,RMVar_hsa_circ_187285 42234 RMVar_ID_42234 Human_SNP_ID_633378218 A-to-I Human chr17 + 77300177 77300177 77300177 TGGAGTGCAGTGGCATGATGTTGGCTCACTGCAGCCTCCACCTCCTGGGTTCTAGCAATTCTTCT TGGAGTGCAGTGGCATGATGTTGGCTCACTGCCGCCTCCACCTCCTGGGTTCTAGCAATTCTTCT A C SEPTIN9 Ensembl:ENSG00000184640 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1468612852 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_340134 42235 RMVar_ID_42235 Human_SNP_ID_633381830 A-to-I Human chr17 + 77313754 77313754 77313754 AAGTCTTTTTTTTTTCTTTTTTCTTTCTAGGCAGGGTCTTTCTCTGTCCCCCAGGCTGGAGTGCA AAGTCTTTTTTTTTTCTTTTTTCTTTCTAGGCCGGGTCTTTCTCTGTCCCCCAGGCTGGAGTGCA A C SEPTIN9 Ensembl:ENSG00000184640 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1567988025 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2523671,Human_RBP_ID_13178040 RMVar_hsa_circ_360688 42236 RMVar_ID_42236 Human_SNP_ID_633393842 A-to-I Human chr17 + 77360018 77360018 77360018 CATCTGTACTACAAATACAAAATTAGCTGGGCATGGTGGTGGGCACCTGTGATCCCAGCTACTTG CATCTGTACTACAAATACAAAATTAGCTGGGCGTGGTGGTGGGCACCTGTGATCCCAGCTACTTG A G SEPTIN9 Ensembl:ENSG00000184640 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs762323167 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_360688 42237 RMVar_ID_42237 Human_SNP_ID_633393858 A-to-I Human chr17 + 77360106 77360106 77360106 TTGAACCCAGGAGGCGGAGGTTGCAGTGAGCCAAGATCACACCATTGCACTCCAGCCTGGAGAAA TTGAACCCAGGAGGCGGAGGTTGCAGTGAGCCGAGATCACACCATTGCACTCCAGCCTGGAGAAA A G SEPTIN9 Ensembl:ENSG00000184640 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs967803499 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_360688 42238 RMVar_ID_42238 Human_SNP_ID_633408325 A-to-I Human chr17 + 77412605 77412605 77412605 CAAAAATTAGCTGGGTGAGGTGGTGCGCCTGTAGTCCCGGCTACTCGGGAGGCTGATGTGGGAGG CAAAAATTAGCTGGGTGAGGTGGTGCGCCTGTGGTCCCGGCTACTCGGGAGGCTGATGTGGGAGG A G SEPTIN9 Ensembl:ENSG00000184640 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928669091 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13178317 RMVar_hsa_circ_52125 42239 RMVar_ID_42239 Human_SNP_ID_633416274 A-to-I Human chr17 + 77442382 77442381 77442383 ACCACGCCTGGCTAATTTTTTGTATTTTTAGTAGAGACAGGGTTTCACTATGTTGGCCAGGCTGG ACCACGCCTGGCTAATTTTTTGTATTTTTAGT__AGACAGGGTTTCACTATGTTGGCCAGGCTGG TAG T SEPTIN9 Ensembl:ENSG00000184640 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1271385072 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_52125 42240 RMVar_ID_42240 Human_SNP_ID_633416275 A-to-I Human chr17 + 77442388 77442388 77442388 CCTGGCTAATTTTTTGTATTTTTAGTAGAGACAGGGTTTCACTATGTTGGCCAGGCTGGTCTCAA CCTGGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACTATGTTGGCCAGGCTGGTCTCAA A G SEPTIN9 Ensembl:ENSG00000184640 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs372572677 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_52125 42241 RMVar_ID_42241 Human_SNP_ID_633422151 A-to-I Human chr17 + 77464292 77464292 77464292 TAGAGACGGTGTTTCACCAGGTTGACCAGGCTAGTCTCGAACCCCTGACCTCAAATAATTGGCCC TAGAGACGGTGTTTCACCAGGTTGACCAGGCTCGTCTCGAACCCCTGACCTCAAATAATTGGCCC A C SEPTIN9 Ensembl:ENSG00000184640 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1359021051 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_52125 42242 RMVar_ID_42242 Human_SNP_ID_633430757 A-to-I Human chr17 + 77491267 77491267 77491267 GAGAAAGGGTCTGGCTCAGTTGCCAAGGTTGCAATGTAGTGGCACAATCATGGCTCACTGCAGCC GAGAAAGGGTCTGGCTCAGTTGCCAAGGTTGCGATGTAGTGGCACAATCATGGCTCACTGCAGCC A G SEPTIN9 Ensembl:ENSG00000184640 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910966083 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_314705,RMVar_hsa_circ_187290,RMVar_hsa_circ_71670 42243 RMVar_ID_42243 Human_SNP_ID_633447517 A-to-I Human chr17 + 77553304 77553304 77553304 AGCTGGGCTCGGTGGCTCATACCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGTCAGATTGCT AGCTGGGCTCGGTGGCTCATACCTGTAATCCCGGCACTTTGGGAGGCCAAGGCAGTCAGATTGCT A G AC021683.2 Ensembl:ENSG00000267506 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs370503683 Functional Loss SNV dbSNP153 33..33 33 - - - 42244 RMVar_ID_42244 Human_SNP_ID_633447547 A-to-I Human chr17 + 77553454 77553454 77553454 GTGGCACATGCCTGTGGTCCCAGCTAGTTGGAAAGCTGAGGTGGGAGGTTGGCTTGAACCCAGGA GTGGCACATGCCTGTGGTCCCAGCTAGTTGGAGAGCTGAGGTGGGAGGTTGGCTTGAACCCAGGA A G AC021683.2 Ensembl:ENSG00000267506 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs994812653 Functional Loss SNV dbSNP153 33..33 33 - - - 42245 RMVar_ID_42245 Human_SNP_ID_633447562 A-to-I Human chr17 + 77553527 77553527 77553527 CTGCAGTGAGCCGTATTGTGCCACTGCACTTCAGCCTGGGCAACAGAGCGAGACCCTGTCTCAAA CTGCAGTGAGCCGTATTGTGCCACTGCACTTCGGCCTGGGCAACAGAGCGAGACCCTGTCTCAAA A G AC021683.2 Ensembl:ENSG00000267506 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1252711857 Functional Loss SNV dbSNP153 33..33 33 - - - 42246 RMVar_ID_42246 Human_SNP_ID_633447793 A-to-I Human chr17 + 77554240 77554240 77554240 CAGGCTGGAGTGCAGTGGCACAATCTCGGTTCACTGCAAGCTCTGCCTCCTGGGTTCACGCCATT CAGGCTGGAGTGCAGTGGCACAATCTCGGTTCGCTGCAAGCTCTGCCTCCTGGGTTCACGCCATT A G AC021683.2 Ensembl:ENSG00000267506 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1379620177 Functional Loss SNV dbSNP153 33..33 33 - - - 42247 RMVar_ID_42247 Human_SNP_ID_633447806 A-to-I Human chr17 + 77554283 77554283 77554283 TGCCTCCTGGGTTCACGCCATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCACCTG TGCCTCCTGGGTTCACGCCATTCTCCTGCCTCGGCCTCCCAAGTAGCTGGGACTACAGGCACCTG A G AC021683.2 Ensembl:ENSG00000267506 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1157637713 Functional Loss SNV dbSNP153 33..33 33 - - - 42248 RMVar_ID_42248 Human_SNP_ID_633447896 A-to-I Human chr17 + 77554739 77554739 77554739 CAACATGGCGAAACCCCATCTCTACTAAAAATACAAAAATTAGCTGGGCATGGTGGCACACGCCT CAACATGGCGAAACCCCATCTCTACTAAAAATGCAAAAATTAGCTGGGCATGGTGGCACACGCCT A G AC021683.2 Ensembl:ENSG00000267506 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs907318543 Functional Loss SNV dbSNP153 33..33 33 - - - 42249 RMVar_ID_42249 Human_SNP_ID_633447922 A-to-I Human chr17 + 77554839 77554839 77554839 ATTGCTGGAACCCGGGAGGTGGAGGTTGCAGTAAGCCAAGATTGAGCCATTGCACTCCAGCCTGG ATTGCTGGAACCCGGGAGGTGGAGGTTGCAGTGAGCCAAGATTGAGCCATTGCACTCCAGCCTGG A G AC021683.2 Ensembl:ENSG00000267506 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1426997809 Functional Loss SNV dbSNP153 33..33 33 - - - 42250 RMVar_ID_42250 Human_SNP_ID_633451591 A-to-I Human chr17 + 77568331 77568331 77568331 GAGTTTTGCTCTTGTTGCCCAGGCTAGAGTGCAATGGCATGATCTTGGCTCACCTCAACCTCCGC GAGTTTTGCTCTTGTTGCCCAGGCTAGAGTGCGATGGCATGATCTTGGCTCACCTCAACCTCCGC A G - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs761208094 Functional Loss SNV dbSNP153 33..33 33 - - - 42251 RMVar_ID_42251 Human_SNP_ID_633595038 A-to-I Human chr17 + 78104702 78104702 78104702 GGAACGCCCCGTGCCTGGGTGGCAAGGGGAGCAGTGAGCTGCTGTGGGGCGGGGTGCCCCAGTAC GGAACGCCCCGTGCCTGGGTGGCAAGGGGAGCCGTGAGCTGCTGTGGGGCGGGGTGCCCCAGTAC A C TNRC6C Ensembl:ENSG00000078687 Protein coding CDS GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs979002118 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6647964 42252 RMVar_ID_42252 Human_SNP_ID_633595039 A-to-I Human chr17 + 78104702 78104702 78104702 GGAACGCCCCGTGCCTGGGTGGCAAGGGGAGCAGTGAGCTGCTGTGGGGCGGGGTGCCCCAGTAC GGAACGCCCCGTGCCTGGGTGGCAAGGGGAGCGGTGAGCTGCTGTGGGGCGGGGTGCCCCAGTAC A G TNRC6C Ensembl:ENSG00000078687 Protein coding CDS GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs979002118 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6647964 42253 RMVar_ID_42253 Human_SNP_ID_633596413 A-to-I Human chr17 - 78109040 78109040 78109040 CGAGATCAGCCTGGGCAACATGGTGAGACCCTATCTCTACAAAAATAAAAAATGAAATGAGCTGG CGAGATCAGCCTGGGCAACATGGTGAGACCCTGTCTCTACAAAAATAAAAAATGAAATGAGCTGG T C TNRC6C-AS1 Ensembl:ENSG00000204282 lincRNA exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1339183229 Functional Loss SNV dbSNP153 33..33 33 - - - 42254 RMVar_ID_42254 Human_SNP_ID_633596619 A-to-I Human chr17 - 78109579 78109579 78109579 TTGCCCATCCCGGAGCACAGTGGCACGATCACAGCTCACTGCAGCCTCGACCTCCTGGGCTCAGG TTGCCCATCCCGGAGCACAGTGGCACGATCACGGCTCACTGCAGCCTCGACCTCCTGGGCTCAGG T C TNRC6C-AS1 Ensembl:ENSG00000204282 lincRNA exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1341908091 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8193432 42255 RMVar_ID_42255 Human_SNP_ID_633596865 A-to-I Human chr17 - 78110341 78110341 78110341 CCAGGCCTGGCTGATCTTCGTATTTTTAGTAGAGATGGGGTTTCACCATGATGGTCAGGCTGGTC CCAGGCCTGGCTGATCTTCGTATTTTTAGTAGTGATGGGGTTTCACCATGATGGTCAGGCTGGTC T A TNRC6C-AS1 Ensembl:ENSG00000204282 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs921338093 Functional Loss SNV dbSNP153 33..33 33 - - - 42256 RMVar_ID_42256 Human_SNP_ID_633596904 A-to-I Human chr17 - 78110464 78110462 78110464 GCCCAAGAGTTTCGGTTTATTTGCTTTTTCAGAGTCTTGCTCTTGCCCAGGCTGGAGTGCAGTTC GCCCAAGAGTTTCGGTTTATTTGCTTTTTCAG__TCTTGCTCTTGCCCAGGCTGGAGTGCAGTTC ACT A TMC6,TNRC6C-AS1 Ensembl:ENSG00000141524,Ensembl:ENSG00000204282 Protein coding,lincRNA 3'UTR,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs975990025 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_8193745,Human_RBP_ID_26458322 Human_miRNA_ID_1377978,Human_miRNA_ID_3175781 42257 RMVar_ID_42257 Human_SNP_ID_633596905 A-to-I Human chr17 - 78110464 78110464 78110464 GCCCAAGAGTTTCGGTTTATTTGCTTTTTCAGAGTCTTGCTCTTGCCCAGGCTGGAGTGCAGTTC GCCCAAGAGTTTCGGTTTATTTGCTTTTTCAGCGTCTTGCTCTTGCCCAGGCTGGAGTGCAGTTC T G TMC6,TNRC6C-AS1 Ensembl:ENSG00000141524,Ensembl:ENSG00000204282 Protein coding,lincRNA 3'UTR,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1340377883 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8193745,Human_RBP_ID_26458322 Human_miRNA_ID_1377978,Human_miRNA_ID_3175781 42258 RMVar_ID_42258 Human_SNP_ID_633596929 A-to-I Human chr17 - 78110522 78110522 78110522 TGGTGGCGCCTGTCTGTAATTGCAGCTGCTCCAGAGGCTGAGGCGGAGGATTGCTTGAGCCCAAG TGGTGGCGCCTGTCTGTAATTGCAGCTGCTCCGGAGGCTGAGGCGGAGGATTGCTTGAGCCCAAG T C TMC6,TNRC6C-AS1 Ensembl:ENSG00000141524,Ensembl:ENSG00000204282 Protein coding,lincRNA 3'UTR,exon GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs569315829 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5098597,Human_RBP_ID_26459916 42259 RMVar_ID_42259 Human_SNP_ID_633599075 A-to-I Human chr17 - 78116334 78116334 78116334 AGGTTGAGGCTGCAGTGAGCTATGATTGTGCCACTGCGCTCCAGCCTGGGTGACAGTGAAACTCT AGGTTGAGGCTGCAGTGAGCTATGATTGTGCCGCTGCGCTCCAGCCTGGGTGACAGTGAAACTCT T C TMC6 Ensembl:ENSG00000141524 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1034798668 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121248,RMVar_hsa_circ_78197,RMVar_hsa_circ_96051,RMVar_hsa_circ_187311,RMVar_hsa_circ_187312,RMVar_hsa_circ_187313 42260 RMVar_ID_42260 Human_SNP_ID_633599083 A-to-I Human chr17 - 78116353 78116353 78116353 GAGGAGATTGCTTGAGCCCAGGTTGAGGCTGCAGTGAGCTATGATTGTGCCACTGCGCTCCAGCC GAGGAGATTGCTTGAGCCCAGGTTGAGGCTGCGGTGAGCTATGATTGTGCCACTGCGCTCCAGCC T C TMC6 Ensembl:ENSG00000141524 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs577453863 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121248,RMVar_hsa_circ_78197,RMVar_hsa_circ_96051,RMVar_hsa_circ_187311,RMVar_hsa_circ_187312,RMVar_hsa_circ_187313 42261 RMVar_ID_42261 Human_SNP_ID_633599101 A-to-I Human chr17 - 78116411 78116411 78116411 AAAGTTAGCTGGGTGTGGTGGTGTGCACCTGTAGTCCCAGCTACTTGGGAGGCTGAGGGAGGAGA AAAGTTAGCTGGGTGTGGTGGTGTGCACCTGTGGTCCCAGCTACTTGGGAGGCTGAGGGAGGAGA T C TMC6 Ensembl:ENSG00000141524 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1445785257 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121248,RMVar_hsa_circ_78197,RMVar_hsa_circ_96051,RMVar_hsa_circ_187311,RMVar_hsa_circ_187312,RMVar_hsa_circ_187313 42262 RMVar_ID_42262 Human_SNP_ID_633599240 A-to-I Human chr17 - 78116834 78116833 78116835 GCTCTGTCACCCAGGCTGGAGTGCAGTGGCACAGTCTCAGCTGACTGCAACCTCTGCCTCCTGGG GCTCTGTCACCCAGGCTGGAGTGCAGTGGCA__GTCTCAGCTGACTGCAACCTCTGCCTCCTGGG CTG C TMC6 Ensembl:ENSG00000141524 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1207677435 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_121248,RMVar_hsa_circ_78197,RMVar_hsa_circ_96051,RMVar_hsa_circ_187311,RMVar_hsa_circ_187312,RMVar_hsa_circ_187313 42263 RMVar_ID_42263 Human_SNP_ID_633599241 A-to-I Human chr17 - 78116834 78116834 78116834 GCTCTGTCACCCAGGCTGGAGTGCAGTGGCACAGTCTCAGCTGACTGCAACCTCTGCCTCCTGGG GCTCTGTCACCCAGGCTGGAGTGCAGTGGCACTGTCTCAGCTGACTGCAACCTCTGCCTCCTGGG T A TMC6 Ensembl:ENSG00000141524 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs561980928 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121248,RMVar_hsa_circ_78197,RMVar_hsa_circ_96051,RMVar_hsa_circ_187311,RMVar_hsa_circ_187312,RMVar_hsa_circ_187313 42264 RMVar_ID_42264 Human_SNP_ID_633599242 A-to-I Human chr17 - 78116834 78116834 78116834 GCTCTGTCACCCAGGCTGGAGTGCAGTGGCACAGTCTCAGCTGACTGCAACCTCTGCCTCCTGGG GCTCTGTCACCCAGGCTGGAGTGCAGTGGCACCGTCTCAGCTGACTGCAACCTCTGCCTCCTGGG T G TMC6 Ensembl:ENSG00000141524 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs561980928 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121248,RMVar_hsa_circ_78197,RMVar_hsa_circ_96051,RMVar_hsa_circ_187311,RMVar_hsa_circ_187312,RMVar_hsa_circ_187313 42265 RMVar_ID_42265 Human_SNP_ID_633608012 A-to-I Human chr17 + 78141342 78141342 78141342 TTAAAATGTCTATTTTTTATTGTGTTTTTTATAATATACATAATCTATTAGTATAGTATCTCTTG TTAAAATGTCTATTTTTTATTGTGTTTTTTATGATATACATAATCTATTAGTATAGTATCTCTTG A G TMC8 Ensembl:ENSG00000167895 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs549083356 Functional Loss SNV dbSNP153 33..33 33 - - - 42266 RMVar_ID_42266 Human_SNP_ID_633613542 A-to-I Human chr17 + 78160374 78160364 78160374 CCTGACCAACATGGTGAAACCCTGTCTCTACTAAAAATACAAAAATTAGCCAGGCGTGGTGGCAC CCTGACCAACATGGTGAAACCCT__________AAAATACAAAAATTAGCCAGGCGTGGTGGCAC TGTCTCTACTA T C17orf99 Ensembl:ENSG00000187997 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1316899251 Functional Loss DEL dbSNP153 24..33 33 - - - 42267 RMVar_ID_42267 Human_SNP_ID_633613564 A-to-I Human chr17 + 78160442 78160442 78160442 CCTGCAGTCCCAGCTATTCGGGAGGCTGAAGCAGGAGAATCACTTGAACTCAGGAGGCGAAGGTT CCTGCAGTCCCAGCTATTCGGGAGGCTGAAGCGGGAGAATCACTTGAACTCAGGAGGCGAAGGTT A G C17orf99 Ensembl:ENSG00000187997 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs111851312 Functional Loss SNV dbSNP153 33..33 33 - - - 42268 RMVar_ID_42268 Human_SNP_ID_633613689 A-to-I Human chr17 + 78160763 78160763 78160763 GCACCACCACGCCCGGCTAATTTTTGTATTTTAGTAGAGACAGACTTTCACCATGTTGGCTACAC GCACCACCACGCCCGGCTAATTTTTGTATTTTGGTAGAGACAGACTTTCACCATGTTGGCTACAC A G C17orf99 Ensembl:ENSG00000187997 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1281159802 Functional Loss SNV dbSNP153 33..33 33 - - - 42269 RMVar_ID_42269 Human_SNP_ID_633619052 A-to-I Human chr17 - 78178074 78178074 78178074 TTGAGGTCAGGAGTTTGAGACCAGCCAGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACA TTGAGGTCAGGAGTTTGAGACCAGCCAGGCCAGCATGGTGAAACCCCATCTCTACTAAAAATACA T C TK1 Ensembl:ENSG00000167900 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1447898247 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85517,RMVar_hsa_circ_187319,RMVar_hsa_circ_76224,RMVar_hsa_circ_187318 42270 RMVar_ID_42270 Human_SNP_ID_633619064 A-to-I Human chr17 - 78178150 78178150 78178150 AACTTTTTTTCTGGCTGGGCACGGTGGCTCACACCTGTAATCCCAGCACTTTGGAAGGCCTAGGC AACTTTTTTTCTGGCTGGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGAAGGCCTAGGC T C TK1 Ensembl:ENSG00000167900 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1011972533 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85517,RMVar_hsa_circ_187319,RMVar_hsa_circ_76224,RMVar_hsa_circ_187318 42271 RMVar_ID_42271 Human_SNP_ID_633619519 A-to-I Human chr17 - 78179904 78179904 78179904 ACCATGCCCAGCTAACCTTTTGTATTTTTAGTAGAGACGGGGTTTCATCATGTTGACCGGGCTGG ACCATGCCCAGCTAACCTTTTGTATTTTTAGTGGAGACGGGGTTTCATCATGTTGACCGGGCTGG T C TK1 Ensembl:ENSG00000167900 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1213633484 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85517,RMVar_hsa_circ_187319,RMVar_hsa_circ_76224,RMVar_hsa_circ_187318 42272 RMVar_ID_42272 Human_SNP_ID_633619541 A-to-I Human chr17 - 78180011 78180011 78180011 GCTGGAGTGCAGTGGCGCAGTCTCGGCTCACTATAACCTCCATCTCCCAGGTTCAAGTGATTCTC GCTGGAGTGCAGTGGCGCAGTCTCGGCTCACTGTAACCTCCATCTCCCAGGTTCAAGTGATTCTC T C TK1 Ensembl:ENSG00000167900 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs895653463 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85517,RMVar_hsa_circ_187319,RMVar_hsa_circ_76224,RMVar_hsa_circ_187318 42273 RMVar_ID_42273 Human_SNP_ID_633620087 A-to-I Human chr17 - 78182209 78182209 78182209 CCACCACGCCCAGCTAATTTTATATTTTTAGTAGAGATGGGGTTTCTCCATGTTGGTCAAGCTGG CCACCACGCCCAGCTAATTTTATATTTTTAGTGGAGATGGGGTTTCTCCATGTTGGTCAAGCTGG T C TK1 Ensembl:ENSG00000167900 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1290411324 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85517,RMVar_hsa_circ_187319,RMVar_hsa_circ_76224,RMVar_hsa_circ_187318 42274 RMVar_ID_42274 Human_SNP_ID_633623168 A-to-I Human chr17 + 78192279 78192279 78192279 GTGATTCGCCCTCCTCGGCCTCCCAAAGTGCTAGGATTACAGGTGTGAGCCACCATGGCTGGACT GTGATTCGCCCTCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCATGGCTGGACT A G AFMID Ensembl:ENSG00000183077 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1162741005 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42275 RMVar_ID_42275 Human_SNP_ID_633623275 A-to-I Human chr17 + 78192588 78192588 78192588 CACCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTATGAGCCACCGTGCCTGGACTTTCACC CACCTGCCTCGGCCTCCCAAAGTGCTGGGATTGCAGGTATGAGCCACCGTGCCTGGACTTTCACC A G AFMID Ensembl:ENSG00000183077 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1488646100 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22717568 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 42276 RMVar_ID_42276 Human_SNP_ID_633623642 A-to-I Human chr17 + 78193700 78193700 78193700 AATAACCTGCCTCTACAAAAAATTTAAAGGCCAGGCGTGGCAGCTCACGCATGTAATCCCAGCAC AATAACCTGCCTCTACAAAAAATTTAAAGGCCTGGCGTGGCAGCTCACGCATGTAATCCCAGCAC A T AFMID Ensembl:ENSG00000183077 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs928860908 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13180063,Human_RBP_ID_17565648,Human_RBP_ID_22717570 RMVar_hsa_circ_101293,RMVar_hsa_circ_120249,RMVar_hsa_circ_119104,RMVar_hsa_circ_374983,RMVar_hsa_circ_187322,RMVar_hsa_circ_118921,RMVar_hsa_circ_187324,RMVar_hsa_circ_187326,RMVar_hsa_circ_187327,RMVar_hsa_circ_187325 42277 RMVar_ID_42277 Human_SNP_ID_633623971 A-to-I Human chr17 + 78194750 78194750 78194750 AGTTTTGCTCTTGTTGTCCAGGCTTGGAGTGCAATGGCGCAATCTCGGCTCACCGCAACCTCCGC AGTTTTGCTCTTGTTGTCCAGGCTTGGAGTGCGATGGCGCAATCTCGGCTCACCGCAACCTCCGC A G AFMID Ensembl:ENSG00000183077 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946246486 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17567105 RMVar_hsa_circ_101293,RMVar_hsa_circ_120249,RMVar_hsa_circ_119104,RMVar_hsa_circ_374983,RMVar_hsa_circ_187322,RMVar_hsa_circ_118921,RMVar_hsa_circ_187324,RMVar_hsa_circ_187326,RMVar_hsa_circ_187327,RMVar_hsa_circ_187325 42278 RMVar_ID_42278 Human_SNP_ID_633624137 A-to-I Human chr17 + 78195294 78195294 78195294 TCATCTCACTGCAACCTCCACCTCCTGGGTTCAAGCAGTTCTTGTGCCTCAGCTGCCCGAATAGC TCATCTCACTGCAACCTCCACCTCCTGGGTTCGAGCAGTTCTTGTGCCTCAGCTGCCCGAATAGC A G AFMID Ensembl:ENSG00000183077 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs181378716 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101293,RMVar_hsa_circ_120249,RMVar_hsa_circ_119104,RMVar_hsa_circ_374983,RMVar_hsa_circ_187322,RMVar_hsa_circ_118921,RMVar_hsa_circ_187324,RMVar_hsa_circ_187326,RMVar_hsa_circ_187327,RMVar_hsa_circ_187325 42279 RMVar_ID_42279 Human_SNP_ID_633624362 A-to-I Human chr17 + 78196100 78196100 78196100 TTATTTCTAACCCAGGCTGGGCTCCATGGCTCATCCCTGTAATCCCAGCACTTTGGGAGGCCAAG TTATTTCTAACCCAGGCTGGGCTCCATGGCTCGTCCCTGTAATCCCAGCACTTTGGGAGGCCAAG A G AFMID Ensembl:ENSG00000183077 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1217183688 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17567109,Human_RBP_ID_22475768,Human_RBP_ID_23171990 RMVar_hsa_circ_101293,RMVar_hsa_circ_120249,RMVar_hsa_circ_119104,RMVar_hsa_circ_374983,RMVar_hsa_circ_187322,RMVar_hsa_circ_118921,RMVar_hsa_circ_187324,RMVar_hsa_circ_187326,RMVar_hsa_circ_187327,RMVar_hsa_circ_187325 42280 RMVar_ID_42280 Human_SNP_ID_633624382 A-to-I Human chr17 + 78196178 78196178 78196178 CTTGAGGTCAAGAGTTCACGGCCAGCCTGGCCAACATAGTGAAACCCCATCTCTACTAAAAACAC CTTGAGGTCAAGAGTTCACGGCCAGCCTGGCCGACATAGTGAAACCCCATCTCTACTAAAAACAC A G AFMID Ensembl:ENSG00000183077 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs559611659 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101293,RMVar_hsa_circ_120249,RMVar_hsa_circ_119104,RMVar_hsa_circ_374983,RMVar_hsa_circ_187322,RMVar_hsa_circ_118921,RMVar_hsa_circ_187324,RMVar_hsa_circ_187326,RMVar_hsa_circ_187327,RMVar_hsa_circ_187325 42281 RMVar_ID_42281 Human_SNP_ID_633624388 A-to-I Human chr17 + 78196213 78196213 78196213 ATAGTGAAACCCCATCTCTACTAAAAACACAAAAAGTAGCCAGGCATGGTGGCGTGCGCCTATAA ATAGTGAAACCCCATCTCTACTAAAAACACAAGAAGTAGCCAGGCATGGTGGCGTGCGCCTATAA A G AFMID Ensembl:ENSG00000183077 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1225309969 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101293,RMVar_hsa_circ_120249,RMVar_hsa_circ_119104,RMVar_hsa_circ_374983,RMVar_hsa_circ_187322,RMVar_hsa_circ_118921,RMVar_hsa_circ_187324,RMVar_hsa_circ_187326,RMVar_hsa_circ_187327,RMVar_hsa_circ_187325 42282 RMVar_ID_42282 Human_SNP_ID_633624411 A-to-I Human chr17 + 78196297 78196297 78196297 CAAGGCAAGAGAATTGCTTGAACTCAGGAGGCAGAGGTTGCAATGAGCAAAGATTGCACCACTGC CAAGGCAAGAGAATTGCTTGAACTCAGGAGGCCGAGGTTGCAATGAGCAAAGATTGCACCACTGC A C AFMID Ensembl:ENSG00000183077 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs980580967 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101293,RMVar_hsa_circ_120249,RMVar_hsa_circ_119104,RMVar_hsa_circ_374983,RMVar_hsa_circ_187322,RMVar_hsa_circ_118921,RMVar_hsa_circ_187324,RMVar_hsa_circ_187326,RMVar_hsa_circ_187327,RMVar_hsa_circ_187325 42283 RMVar_ID_42283 Human_SNP_ID_633624465 A-to-I Human chr17 + 78196536 78196536 78196536 CACCTTCTCTACTGAAAATACAAAAATGAGCCAGGCATAGTGGCACATGCCTGTAATCCCAGCCA CACCTTCTCTACTGAAAATACAAAAATGAGCCGGGCATAGTGGCACATGCCTGTAATCCCAGCCA A G AFMID Ensembl:ENSG00000183077 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1456248605 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101293,RMVar_hsa_circ_120249,RMVar_hsa_circ_119104,RMVar_hsa_circ_374983,RMVar_hsa_circ_187322,RMVar_hsa_circ_118921,RMVar_hsa_circ_187324,RMVar_hsa_circ_187326,RMVar_hsa_circ_187327,RMVar_hsa_circ_187325 42284 RMVar_ID_42284 Human_SNP_ID_633624467 A-to-I Human chr17 + 78196540 78196540 78196540 TTCTCTACTGAAAATACAAAAATGAGCCAGGCATAGTGGCACATGCCTGTAATCCCAGCCACCGG TTCTCTACTGAAAATACAAAAATGAGCCAGGCCTAGTGGCACATGCCTGTAATCCCAGCCACCGG A C AFMID Ensembl:ENSG00000183077 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1025174511 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101293,RMVar_hsa_circ_120249,RMVar_hsa_circ_119104,RMVar_hsa_circ_374983,RMVar_hsa_circ_187322,RMVar_hsa_circ_118921,RMVar_hsa_circ_187324,RMVar_hsa_circ_187326,RMVar_hsa_circ_187327,RMVar_hsa_circ_187325 42285 RMVar_ID_42285 Human_SNP_ID_633624468 A-to-I Human chr17 + 78196540 78196540 78196540 TTCTCTACTGAAAATACAAAAATGAGCCAGGCATAGTGGCACATGCCTGTAATCCCAGCCACCGG TTCTCTACTGAAAATACAAAAATGAGCCAGGCGTAGTGGCACATGCCTGTAATCCCAGCCACCGG A G AFMID Ensembl:ENSG00000183077 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1025174511 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101293,RMVar_hsa_circ_120249,RMVar_hsa_circ_119104,RMVar_hsa_circ_374983,RMVar_hsa_circ_187322,RMVar_hsa_circ_118921,RMVar_hsa_circ_187324,RMVar_hsa_circ_187326,RMVar_hsa_circ_187327,RMVar_hsa_circ_187325 42286 RMVar_ID_42286 Human_SNP_ID_633624871 A-to-I Human chr17 + 78198162 78198162 78198162 GAGGTGGGAAGCTTGTTTGAACCTAGGAGGTTAAGGCTGCAGTAAGCCGAGATTGCACCACTACA GAGGTGGGAAGCTTGTTTGAACCTAGGAGGTTGAGGCTGCAGTAAGCCGAGATTGCACCACTACA A G AFMID Ensembl:ENSG00000183077 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1265904095 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13180129,Human_RBP_ID_17567111 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 42287 RMVar_ID_42287 Human_SNP_ID_633625053 A-to-I Human chr17 + 78198702 78198702 78198702 GTGGTGGCGCACACCTGTAATCCCAGCTGCTCAGAAGGAGGAGACAGGAGAATCACTTGAACCCC GTGGTGGCGCACACCTGTAATCCCAGCTGCTCGGAAGGAGGAGACAGGAGAATCACTTGAACCCC A G AFMID Ensembl:ENSG00000183077 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1323329137 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13180131 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 42288 RMVar_ID_42288 Human_SNP_ID_633625490 A-to-I Human chr17 + 78200329 78200329 78200329 GGCACGCGCCACCACGCCCAGATAATTTTTGTATTTTTAGTAGAGACAGGGTTTTACCATGTTGG GGCACGCGCCACCACGCCCAGATAATTTTTGTTTTTTTAGTAGAGACAGGGTTTTACCATGTTGG A T AFMID Ensembl:ENSG00000183077 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1307628709 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 42289 RMVar_ID_42289 Human_SNP_ID_633625493 A-to-I Human chr17 + 78200344 78200343 78200345 GCCCAGATAATTTTTGTATTTTTAGTAGAGACAGGGTTTTACCATGTTGGCCGGGATGGTCTCAA GCCCAGATAATTTTTGTATTTTTAGTAGAGAC__GGTTTTACCATGTTGGCCGGGATGGTCTCAA CAG C AFMID Ensembl:ENSG00000183077 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs920581840 Functional Loss DEL dbSNP153 33..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 42290 RMVar_ID_42290 Human_SNP_ID_633625768 A-to-I Human chr17 + 78201437 78201437 78201437 GAGGTTGAGCTCGAGACCAGCCTCGCCAATACAGTGAAACCCCGTCTCTACTAAAAATACAAAAA GAGGTTGAGCTCGAGACCAGCCTCGCCAATACGGTGAAACCCCGTCTCTACTAAAAATACAAAAA A G AFMID Ensembl:ENSG00000183077 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs970402418 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 42291 RMVar_ID_42291 Human_SNP_ID_633625769 A-to-I Human chr17 + 78201437 78201437 78201437 GAGGTTGAGCTCGAGACCAGCCTCGCCAATACAGTGAAACCCCGTCTCTACTAAAAATACAAAAA GAGGTTGAGCTCGAGACCAGCCTCGCCAATACTGTGAAACCCCGTCTCTACTAAAAATACAAAAA A T AFMID Ensembl:ENSG00000183077 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs970402418 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 42292 RMVar_ID_42292 Human_SNP_ID_633625783 A-to-I Human chr17 + 78201504 78201504 78201504 AGCCAGGTGTGGTGGCACGGGCCCATAATCCCAGCTACTCAGGAGGCTGAGGCTGGAGGATTGCT AGCCAGGTGTGGTGGCACGGGCCCATAATCCCGGCTACTCAGGAGGCTGAGGCTGGAGGATTGCT A G AFMID Ensembl:ENSG00000183077 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1006185551 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 42293 RMVar_ID_42293 Human_SNP_ID_633626404 A-to-I Human chr17 + 78203135 78203135 78203135 CAGACTGGAACGCAGTGGTGCGACCTCAGCTCACTGCAACTTCTGCCTCCCGGGCTCAAGCAATT CAGACTGGAACGCAGTGGTGCGACCTCAGCTCCCTGCAACTTCTGCCTCCCGGGCTCAAGCAATT A C AFMID Ensembl:ENSG00000183077 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1442763690 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76228,RMVar_hsa_circ_120249,RMVar_hsa_circ_119104,RMVar_hsa_circ_187322,RMVar_hsa_circ_118921,RMVar_hsa_circ_124317,RMVar_hsa_circ_187326,RMVar_hsa_circ_187327,RMVar_hsa_circ_358459,RMVar_hsa_circ_69193,RMVar_hsa_circ_187328,RMVar_hsa_circ_187330 42294 RMVar_ID_42294 Human_SNP_ID_633626405 A-to-I Human chr17 + 78203135 78203135 78203135 CAGACTGGAACGCAGTGGTGCGACCTCAGCTCACTGCAACTTCTGCCTCCCGGGCTCAAGCAATT CAGACTGGAACGCAGTGGTGCGACCTCAGCTCGCTGCAACTTCTGCCTCCCGGGCTCAAGCAATT A G AFMID Ensembl:ENSG00000183077 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1442763690 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76228,RMVar_hsa_circ_120249,RMVar_hsa_circ_119104,RMVar_hsa_circ_187322,RMVar_hsa_circ_118921,RMVar_hsa_circ_124317,RMVar_hsa_circ_187326,RMVar_hsa_circ_187327,RMVar_hsa_circ_358459,RMVar_hsa_circ_69193,RMVar_hsa_circ_187328,RMVar_hsa_circ_187330 42295 RMVar_ID_42295 Human_SNP_ID_633626413 A-to-I Human chr17 + 78203160 78203160 78203160 TCAGCTCACTGCAACTTCTGCCTCCCGGGCTCAAGCAATTCTTCTGCCTCAGCCTCCCAAGTAGC TCAGCTCACTGCAACTTCTGCCTCCCGGGCTCGAGCAATTCTTCTGCCTCAGCCTCCCAAGTAGC A G AFMID Ensembl:ENSG00000183077 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs955393989 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76228,RMVar_hsa_circ_120249,RMVar_hsa_circ_119104,RMVar_hsa_circ_187322,RMVar_hsa_circ_118921,RMVar_hsa_circ_124317,RMVar_hsa_circ_187326,RMVar_hsa_circ_187327,RMVar_hsa_circ_358459,RMVar_hsa_circ_69193,RMVar_hsa_circ_187328,RMVar_hsa_circ_187330 42296 RMVar_ID_42296 Human_SNP_ID_633626419 A-to-I Human chr17 + 78203186 78203186 78203186 GGGCTCAAGCAATTCTTCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGTGCACGCCACCACA GGGCTCAAGCAATTCTTCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGTGCACGCCACCACA A G AFMID Ensembl:ENSG00000183077 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1208895817 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76228,RMVar_hsa_circ_120249,RMVar_hsa_circ_119104,RMVar_hsa_circ_187322,RMVar_hsa_circ_118921,RMVar_hsa_circ_124317,RMVar_hsa_circ_187326,RMVar_hsa_circ_187327,RMVar_hsa_circ_358459,RMVar_hsa_circ_69193,RMVar_hsa_circ_187328,RMVar_hsa_circ_187330 42297 RMVar_ID_42297 Human_SNP_ID_633626441 A-to-I Human chr17 + 78203258 78203258 78203258 AATTTTTGTATTTTTAGTAGAGACAGGGTTTTACCATGTTGGCCAGGCTGGTCTTGAACTCCTGA AATTTTTGTATTTTTAGTAGAGACAGGGTTTTTCCATGTTGGCCAGGCTGGTCTTGAACTCCTGA A T AFMID Ensembl:ENSG00000183077 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs969859725 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76228,RMVar_hsa_circ_120249,RMVar_hsa_circ_119104,RMVar_hsa_circ_187322,RMVar_hsa_circ_118921,RMVar_hsa_circ_124317,RMVar_hsa_circ_187326,RMVar_hsa_circ_187327,RMVar_hsa_circ_358459,RMVar_hsa_circ_69193,RMVar_hsa_circ_187328,RMVar_hsa_circ_187330 42298 RMVar_ID_42298 Human_SNP_ID_633626608 A-to-I Human chr17 + 78203930 78203930 78203930 CCTGTAATCCCAGCTACTCGGGAGGCTAATGCAGGAGAATCACTTGAACCCAGGAGGCGGAGGTT CCTGTAATCCCAGCTACTCGGGAGGCTAATGCGGGAGAATCACTTGAACCCAGGAGGCGGAGGTT A G AFMID Ensembl:ENSG00000183077 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1242660251 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76228,RMVar_hsa_circ_120249,RMVar_hsa_circ_119104,RMVar_hsa_circ_187322,RMVar_hsa_circ_118921,RMVar_hsa_circ_124317,RMVar_hsa_circ_187326,RMVar_hsa_circ_187327,RMVar_hsa_circ_358459,RMVar_hsa_circ_69193,RMVar_hsa_circ_187328,RMVar_hsa_circ_187330 42299 RMVar_ID_42299 Human_SNP_ID_633626700 A-to-I Human chr17 + 78204321 78204321 78204321 GATAAATTTGCTGGGCATAGTGGTGCACACCTATACTCCTGCTTGGGAGGCTGAGGCAGGAGGAT GATAAATTTGCTGGGCATAGTGGTGCACACCTGTACTCCTGCTTGGGAGGCTGAGGCAGGAGGAT A G AFMID Ensembl:ENSG00000183077 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973286723 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17566654 RMVar_hsa_circ_76228,RMVar_hsa_circ_120249,RMVar_hsa_circ_119104,RMVar_hsa_circ_187322,RMVar_hsa_circ_118921,RMVar_hsa_circ_124317,RMVar_hsa_circ_187326,RMVar_hsa_circ_187327,RMVar_hsa_circ_358459,RMVar_hsa_circ_69193,RMVar_hsa_circ_187328,RMVar_hsa_circ_187330 42300 RMVar_ID_42300 Human_SNP_ID_633626701 A-to-I Human chr17 + 78204321 78204321 78204321 GATAAATTTGCTGGGCATAGTGGTGCACACCTATACTCCTGCTTGGGAGGCTGAGGCAGGAGGAT GATAAATTTGCTGGGCATAGTGGTGCACACCTTTACTCCTGCTTGGGAGGCTGAGGCAGGAGGAT A T AFMID Ensembl:ENSG00000183077 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973286723 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17566654 RMVar_hsa_circ_76228,RMVar_hsa_circ_120249,RMVar_hsa_circ_119104,RMVar_hsa_circ_187322,RMVar_hsa_circ_118921,RMVar_hsa_circ_124317,RMVar_hsa_circ_187326,RMVar_hsa_circ_187327,RMVar_hsa_circ_358459,RMVar_hsa_circ_69193,RMVar_hsa_circ_187328,RMVar_hsa_circ_187330 42301 RMVar_ID_42301 Human_SNP_ID_633627514 A-to-I Human chr17 + 78206514 78206514 78206514 AGCTCTCTGCTGCCTCCTGGGCTCAAGTGGTTATCCTGCCCCAGCCTCTCGAGTAGCTGGGACTA AGCTCTCTGCTGCCTCCTGGGCTCAAGTGGTTCTCCTGCCCCAGCCTCTCGAGTAGCTGGGACTA A C AFMID Ensembl:ENSG00000183077 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs528676422 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17566258 42302 RMVar_ID_42302 Human_SNP_ID_633627911 A-to-I Human chr17 + 78207449 78207449 78207449 GGGACTACAGGCGCCTGCCATCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCA GGGACTACAGGCGCCTGCCATCATGCCTGGCTCATTTTTGTATTTTTAGTAGAGACGGGGTTTCA A C AFMID Ensembl:ENSG00000183077 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1297121498 Functional Loss SNV dbSNP153 33..33 33 - - - 42303 RMVar_ID_42303 Human_SNP_ID_633631043 A-to-I Human chr17 + 78217636 78217636 78217636 CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCCGCCACCACACCCGGCTAATTTTT CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTGCAGGCGCCCGCCACCACACCCGGCTAATTTTT A G BIRC5 Ensembl:ENSG00000089685 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1425253759 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_288415 42304 RMVar_ID_42304 Human_SNP_ID_633650794 A-to-I Human chr17 - 78288965 78288965 78288965 AGCCTCCCGAGTAGCTGGGACTACAGGCACGCACCACCATGCCAGGCTAATTTTTGTATTTTTAG AGCCTCCCGAGTAGCTGGGACTACAGGCACGCGCCACCATGCCAGGCTAATTTTTGTATTTTTAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432250435 Functional Loss SNV dbSNP153 33..33 33 - - - 42305 RMVar_ID_42305 Human_SNP_ID_633682784 A-to-I Human chr17 + 78404340 78404340 78404340 GTCTTGCTCTGTTTCCCAGGCTGGACTGCAGTAGCATGATCTCAGTTCACCGCAACCTCCACTTC GTCTTGCTCTGTTTCCCAGGCTGGACTGCAGTTGCATGATCTCAGTTCACCGCAACCTCCACTTC A T PGS1 Ensembl:ENSG00000087157 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1567978197 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_323963,RMVar_hsa_circ_372235,RMVar_hsa_circ_187334,RMVar_hsa_circ_187335,RMVar_hsa_circ_187348,RMVar_hsa_circ_89170,RMVar_hsa_circ_187345,RMVar_hsa_circ_111289,RMVar_hsa_circ_128058,RMVar_hsa_circ_187349,RMVar_hsa_circ_101019,RMVar_hsa_circ_187354,RMVar_hsa_circ_122367,RMVar_hsa_circ_187355 42306 RMVar_ID_42306 Human_SNP_ID_633682925 A-to-I Human chr17 + 78404840 78404840 78404840 GTACCACCACGCCTGACTAATTTTTTATTTTTAGTAGAGATTGGGTTTCTCCATGTTGGTCAGGC GTACCACCACGCCTGACTAATTTTTTATTTTTGGTAGAGATTGGGTTTCTCCATGTTGGTCAGGC A G PGS1 Ensembl:ENSG00000087157 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1163318160 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_323963,RMVar_hsa_circ_372235,RMVar_hsa_circ_187334,RMVar_hsa_circ_187335,RMVar_hsa_circ_187348,RMVar_hsa_circ_89170,RMVar_hsa_circ_187345,RMVar_hsa_circ_111289,RMVar_hsa_circ_128058,RMVar_hsa_circ_187349,RMVar_hsa_circ_101019,RMVar_hsa_circ_187354,RMVar_hsa_circ_122367,RMVar_hsa_circ_187355 42307 RMVar_ID_42307 Human_SNP_ID_633684622 A-to-I Human chr17 + 78410635 78410635 78410635 AGCTGGGATTACAGGCACGCACCAGAATGCCCAGCTAGTTTTTGTATTTTTAGTAGAGATGGGGT AGCTGGGATTACAGGCACGCACCAGAATGCCCGGCTAGTTTTTGTATTTTTAGTAGAGATGGGGT A G PGS1 Ensembl:ENSG00000087157 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1377482966 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_323963,RMVar_hsa_circ_372235,RMVar_hsa_circ_187334,RMVar_hsa_circ_187335,RMVar_hsa_circ_187348,RMVar_hsa_circ_89170,RMVar_hsa_circ_187345,RMVar_hsa_circ_111289,RMVar_hsa_circ_128058,RMVar_hsa_circ_187349,RMVar_hsa_circ_101019,RMVar_hsa_circ_187354,RMVar_hsa_circ_122367,RMVar_hsa_circ_187355 42308 RMVar_ID_42308 Human_SNP_ID_633684627 A-to-I Human chr17 + 78410654 78410654 78410654 CACCAGAATGCCCAGCTAGTTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGATGGCCAGGC CACCAGAATGCCCAGCTAGTTTTTGTATTTTTGGTAGAGATGGGGTTTCACCATGATGGCCAGGC A G PGS1 Ensembl:ENSG00000087157 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1238985601 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_323963,RMVar_hsa_circ_372235,RMVar_hsa_circ_187334,RMVar_hsa_circ_187335,RMVar_hsa_circ_187348,RMVar_hsa_circ_89170,RMVar_hsa_circ_187345,RMVar_hsa_circ_111289,RMVar_hsa_circ_128058,RMVar_hsa_circ_187349,RMVar_hsa_circ_101019,RMVar_hsa_circ_187354,RMVar_hsa_circ_122367,RMVar_hsa_circ_187355 42309 RMVar_ID_42309 Human_SNP_ID_633684638 A-to-I Human chr17 + 78410674 78410674 78410674 TTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGATGGCCAGGCTGGTTTTGAACTCCTGACCT TTTTGTATTTTTAGTAGAGATGGGGTTTCACCGTGATGGCCAGGCTGGTTTTGAACTCCTGACCT A G PGS1 Ensembl:ENSG00000087157 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1407029728 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_323963,RMVar_hsa_circ_372235,RMVar_hsa_circ_187334,RMVar_hsa_circ_187335,RMVar_hsa_circ_187348,RMVar_hsa_circ_89170,RMVar_hsa_circ_187345,RMVar_hsa_circ_111289,RMVar_hsa_circ_128058,RMVar_hsa_circ_187349,RMVar_hsa_circ_101019,RMVar_hsa_circ_187354,RMVar_hsa_circ_122367,RMVar_hsa_circ_187355 42310 RMVar_ID_42310 Human_SNP_ID_633687943 A-to-I Human chr17 + 78421435 78421435 78421435 TGTCACCCTTCATGGGGTCTGAAAGGTTGCATAGGCTCACCTGGTCTTAGACAAGGACAGTTGCA TGTCACCCTTCATGGGGTCTGAAAGGTTGCATGGGCTCACCTGGTCTTAGACAAGGACAGTTGCA A G PGS1 Ensembl:ENSG00000087157 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2138127 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13181777 RMVar_hsa_circ_112282,RMVar_hsa_circ_187358 42311 RMVar_ID_42311 Human_SNP_ID_633688431 A-to-I Human chr17 + 78422542 78422542 78422542 CCCTTTTGAGACAGGGTCTCACTCTGTCACCCAGGCTGGAGTGAGTGGCATGATCATGCCTCGCT CCCTTTTGAGACAGGGTCTCACTCTGTCACCCCGGCTGGAGTGAGTGGCATGATCATGCCTCGCT A C PGS1 Ensembl:ENSG00000087157 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1224859619 Functional Loss SNV dbSNP153 33..33 33 - - - 42312 RMVar_ID_42312 Human_SNP_ID_633688508 A-to-I Human chr17 + 78422734 78422734 78422734 GTTGCCCAGGCTGGTCTTAAACTCCTGGGCTCAAGTAAGATTGCCGTCCTGGGATTAGAGGCGTG GTTGCCCAGGCTGGTCTTAAACTCCTGGGCTCGAGTAAGATTGCCGTCCTGGGATTAGAGGCGTG A G PGS1 Ensembl:ENSG00000087157 Protein coding intron GSE38233;GSE107867 cultured B-cells;ASD brains,cerebellum - 24183664,30559470 RNA-Seq:(High) rs1042902187 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17567121 42313 RMVar_ID_42313 Human_SNP_ID_633688514 A-to-I Human chr17 + 78422758 78422758 78422758 CTGGGCTCAAGTAAGATTGCCGTCCTGGGATTAGAGGCGTGAGCTGCTGCAGCGGCCTGCTTTTC CTGGGCTCAAGTAAGATTGCCGTCCTGGGATTCGAGGCGTGAGCTGCTGCAGCGGCCTGCTTTTC A C PGS1 Ensembl:ENSG00000087157 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,31158229,32596459 RNA-Seq:(High) rs1297467666 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13181850,Human_RBP_ID_17566261 42314 RMVar_ID_42314 Human_SNP_ID_633688520 A-to-I Human chr17 + 78422776 78422773 78422776 GCCGTCCTGGGATTAGAGGCGTGAGCTGCTGCAGCGGCCTGCTTTTCTTTGAAGCCTGAGAAATG GCCGTCCTGGGATTAGAGGCGTGAGCTGCT___GCGGCCTGCTTTTCTTTGAAGCCTGAGAAATG TGCA T PGS1 Ensembl:ENSG00000087157 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1316476152 Functional Loss DEL dbSNP153 31..33 33 - - - Human_RBP_ID_13181851,Human_RBP_ID_17566261 42315 RMVar_ID_42315 Human_SNP_ID_633688544 A-to-I Human chr17 + 78422834 78422834 78422834 AGAAATGTTGAGGGCCGGGCACAGTGGTTGACACCTGTAATCCTGGCGCTTTGGGAGGCCGAGGT AGAAATGTTGAGGGCCGGGCACAGTGGTTGACTCCTGTAATCCTGGCGCTTTGGGAGGCCGAGGT A T PGS1 Ensembl:ENSG00000087157 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1419814866 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13181852 42316 RMVar_ID_42316 Human_SNP_ID_633688578 A-to-I Human chr17 + 78422940 78422940 78422940 CAACATGGTGAAACCCCATCTCTACTAAAAATAAAAAAATTAGCTGCGTGTGGTGGTGGGTGCCT CAACATGGTGAAACCCCATCTCTACTAAAAATGAAAAAATTAGCTGCGTGTGGTGGTGGGTGCCT A G PGS1 Ensembl:ENSG00000087157 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1139218 Functional Loss SNV dbSNP153 33..33 33 - - - 42317 RMVar_ID_42317 Human_SNP_ID_633688598 A-to-I Human chr17 + 78422975 78422975 78422975 AAAATTAGCTGCGTGTGGTGGTGGGTGCCTGTAACCCCAGCTACTTGGGAGGTTGAGGCAGGAGA AAAATTAGCTGCGTGTGGTGGTGGGTGCCTGTCACCCCAGCTACTTGGGAGGTTGAGGCAGGAGA A C PGS1 Ensembl:ENSG00000087157 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1139222 Functional Loss SNV dbSNP153 33..33 33 - - - 42318 RMVar_ID_42318 Human_SNP_ID_633688610 A-to-I Human chr17 + 78423002 78423002 78423002 CCTGTAACCCCAGCTACTTGGGAGGTTGAGGCAGGAGAATCGCTTGAGCCCAGGAGGTGGAGGTT CCTGTAACCCCAGCTACTTGGGAGGTTGAGGCGGGAGAATCGCTTGAGCCCAGGAGGTGGAGGTT A G PGS1 Ensembl:ENSG00000087157 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs1192980024 Functional Loss SNV dbSNP153 33..33 33 - - - 42319 RMVar_ID_42319 Human_SNP_ID_633688613 A-to-I Human chr17 + 78423007 78423007 78423007 AACCCCAGCTACTTGGGAGGTTGAGGCAGGAGAATCGCTTGAGCCCAGGAGGTGGAGGTTGCAAC AACCCCAGCTACTTGGGAGGTTGAGGCAGGAGGATCGCTTGAGCCCAGGAGGTGGAGGTTGCAAC A G PGS1 Ensembl:ENSG00000087157 Protein coding intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1477863350 Functional Loss SNV dbSNP153 33..33 33 - - - 42320 RMVar_ID_42320 Human_SNP_ID_633721713 A-to-I Human chr17 + 78504299 78504299 78504299 GTTAGCCAGGCTGGTCTTGAACTCCCGACCTCAGATGATCCGCCCACCTCGACCTCCCAAAGTGC GTTAGCCAGGCTGGTCTTGAACTCCCGACCTCGGATGATCCGCCCACCTCGACCTCCCAAAGTGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1339617652 Functional Loss SNV dbSNP153 33..33 33 - - - 42321 RMVar_ID_42321 Human_SNP_ID_633780969 A-to-I Human chr17 - 78689474 78689474 78689474 GCTCCACATCCTGTCAGATCAGTGGCGGCGTTAGATTCTCATAGGAGCACGAACCCTATTGTAAA GCTCCACATCCTGTCAGATCAGTGGCGGCGTTCGATTCTCATAGGAGCACGAACCCTATTGTAAA T G CYTH1 Ensembl:ENSG00000108669 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432082612 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_187365,RMVar_hsa_circ_305402,RMVar_hsa_circ_343928,RMVar_hsa_circ_187366,RMVar_hsa_circ_350907 42322 RMVar_ID_42322 Human_SNP_ID_633783648 A-to-I Human chr17 - 78699928 78699928 78699928 AAAATTAGCCAGGTGTGGTGGCTTATGCCTGTAGTCCCGGCTATTTGTGAGGCTGAGGCAGGAGG AAAATTAGCCAGGTGTGGTGGCTTATGCCTGTGGTCCCGGCTATTTGTGAGGCTGAGGCAGGAGG T C CYTH1 Ensembl:ENSG00000108669 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1310441320 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_501542 RMVar_hsa_circ_103,RMVar_hsa_circ_305402,RMVar_hsa_circ_187366,RMVar_hsa_circ_350907,RMVar_hsa_circ_291610,RMVar_hsa_circ_187369,RMVar_hsa_circ_28317,RMVar_hsa_circ_323598 42323 RMVar_ID_42323 Human_SNP_ID_633784404 A-to-I Human chr17 - 78702897 78702897 78702897 GGATCACTTGAGCCCAGGAGGCAGAGGTTGCAATGAGCCGAGATAGCACCACTGCACTTCAGCCT GGATCACTTGAGCCCAGGAGGCAGAGGTTGCAGTGAGCCGAGATAGCACCACTGCACTTCAGCCT T C CYTH1 Ensembl:ENSG00000108669 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs986848933 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103,RMVar_hsa_circ_305402,RMVar_hsa_circ_187366,RMVar_hsa_circ_350907,RMVar_hsa_circ_291610,RMVar_hsa_circ_187369,RMVar_hsa_circ_323598,RMVar_hsa_circ_276093,RMVar_hsa_circ_187371,RMVar_hsa_circ_187372,RMVar_hsa_circ_318022 42324 RMVar_ID_42324 Human_SNP_ID_633784536 A-to-I Human chr17 - 78703397 78703397 78703397 TTTTTTTTTTTTTTTTTTGGAGACGGAGTCTCACTCTGTCACCCGGGCTAGAGTGCAGTGGTGGA TTTTTTTTTTTTTTTTTTGGAGACGGAGTCTCGCTCTGTCACCCGGGCTAGAGTGCAGTGGTGGA T C CYTH1 Ensembl:ENSG00000108669 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1409662999 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13182541 RMVar_hsa_circ_103,RMVar_hsa_circ_305402,RMVar_hsa_circ_187366,RMVar_hsa_circ_350907,RMVar_hsa_circ_291610,RMVar_hsa_circ_187369,RMVar_hsa_circ_323598,RMVar_hsa_circ_276093,RMVar_hsa_circ_187371,RMVar_hsa_circ_187372,RMVar_hsa_circ_318022 42325 RMVar_ID_42325 Human_SNP_ID_633784537 A-to-I Human chr17 - 78703397 78703397 78703397 TTTTTTTTTTTTTTTTTTGGAGACGGAGTCTCACTCTGTCACCCGGGCTAGAGTGCAGTGGTGGA TTTTTTTTTTTTTTTTTTGGAGACGGAGTCTCCCTCTGTCACCCGGGCTAGAGTGCAGTGGTGGA T G CYTH1 Ensembl:ENSG00000108669 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1409662999 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13182541 RMVar_hsa_circ_103,RMVar_hsa_circ_305402,RMVar_hsa_circ_187366,RMVar_hsa_circ_350907,RMVar_hsa_circ_291610,RMVar_hsa_circ_187369,RMVar_hsa_circ_323598,RMVar_hsa_circ_276093,RMVar_hsa_circ_187371,RMVar_hsa_circ_187372,RMVar_hsa_circ_318022 42326 RMVar_ID_42326 Human_SNP_ID_633784846 A-to-I Human chr17 - 78704672 78704671 78704672 ACAAAATATTTTAAAAAGTAGCCAGTTGTGGTAGTATCTGCTTGTAGTCCTAGTTACTCAGGAGG ACAAAATATTTTAAAAAGTAGCCAGTTGTGGT_GTATCTGCTTGTAGTCCTAGTTACTCAGGAGG CT C CYTH1 Ensembl:ENSG00000108669 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1281813319 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_103,RMVar_hsa_circ_305402,RMVar_hsa_circ_187366,RMVar_hsa_circ_350907,RMVar_hsa_circ_291610,RMVar_hsa_circ_187369,RMVar_hsa_circ_323598,RMVar_hsa_circ_276093,RMVar_hsa_circ_187371,RMVar_hsa_circ_187372,RMVar_hsa_circ_318022 42327 RMVar_ID_42327 Human_SNP_ID_633788717 A-to-I Human chr17 - 78720404 78720404 78720404 TGAGGCAGGAGAATTGCATGAACCCAGGAGGCAGAGGTTGCAGTGAGCTGAGGTTGCGGCAGTGC TGAGGCAGGAGAATTGCATGAACCCAGGAGGCGGAGGTTGCAGTGAGCTGAGGTTGCGGCAGTGC T C CYTH1 Ensembl:ENSG00000108669 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1204515513 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13182615,Human_RBP_ID_25328412 42328 RMVar_ID_42328 Human_SNP_ID_633791922 A-to-I Human chr17 - 78732963 78732963 78732963 CCTGCCTCAGGCTCCCGAGTAGCTGGGACTACAGGAACGTACCACCACGCCCGGCTAATTTTTGT CCTGCCTCAGGCTCCCGAGTAGCTGGGACTACGGGAACGTACCACCACGCCCGGCTAATTTTTGT T C CYTH1 Ensembl:ENSG00000108669 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs904986184 Functional Loss SNV dbSNP153 33..33 33 - - - 42329 RMVar_ID_42329 Human_SNP_ID_633792223 A-to-I Human chr17 - 78734045 78734045 78734045 AGGTTTCACCATGTTGGCCAGGCTTGTGTTGAACTCCTGACCTCATGTGATCCACCCACCTTGGC AGGTTTCACCATGTTGGCCAGGCTTGTGTTGAGCTCCTGACCTCATGTGATCCACCCACCTTGGC T C CYTH1 Ensembl:ENSG00000108669 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1176953345 Functional Loss SNV dbSNP153 33..33 33 - - - 42330 RMVar_ID_42330 Human_SNP_ID_633792230 A-to-I Human chr17 - 78734093 78734093 78734093 GGTGCATGCCACCACACCCGGCTAATTTTTGTATTTTTTGCAGAGACGAGGTTTCACCATGTTGG GGTGCATGCCACCACACCCGGCTAATTTTTGTGTTTTTTGCAGAGACGAGGTTTCACCATGTTGG T C CYTH1 Ensembl:ENSG00000108669 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1233923135 Functional Loss SNV dbSNP153 33..33 33 - - - 42331 RMVar_ID_42331 Human_SNP_ID_633795325 A-to-I Human chr17 - 78746794 78746794 78746794 GAGACTACAGGCACGCACCACCACAGCCAGCTAATTTTTTAGTTTTCTGTAGAGACGGAGTCTGT GAGACTACAGGCACGCACCACCACAGCCAGCTGATTTTTTAGTTTTCTGTAGAGACGGAGTCTGT T C CYTH1 Ensembl:ENSG00000108669 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1238860839 Functional Loss SNV dbSNP153 33..33 33 - - - 42332 RMVar_ID_42332 Human_SNP_ID_633796028 A-to-I Human chr17 - 78749625 78749625 78749625 ATTTTTATTTGTTATTATTATTTTTTTGAGACAGGGATCTCAATTTGTCACCCAGGCTGGAATAT ATTTTTATTTGTTATTATTATTTTTTTGAGACGGGGATCTCAATTTGTCACCCAGGCTGGAATAT T C CYTH1 Ensembl:ENSG00000108669 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900884906 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13182995 42333 RMVar_ID_42333 Human_SNP_ID_633796920 A-to-I Human chr17 - 78753243 78753243 78753243 ATTGCCCAGGCTGGTCTAGAACTCCTGGCCTCAAGCAATTCTCCCACCTCAGCCTCCCAACGTGC ATTGCCCAGGCTGGTCTAGAACTCCTGGCCTCCAGCAATTCTCCCACCTCAGCCTCCCAACGTGC T G CYTH1 Ensembl:ENSG00000108669 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs927833243 Functional Loss SNV dbSNP153 33..33 33 - - - 42334 RMVar_ID_42334 Human_SNP_ID_633807488 A-to-I Human chr17 - 78790227 78790225 78790227 AAATTAGCCAGGCGTGGTGGTGGGTGCCTGTAATCCCAGCTATTCAGGGAGGCTGAGGCAGAGGA AAATTAGCCAGGCGTGGTGGTGGGTGCCTGTA__CCCAGCTATTCAGGGAGGCTGAGGCAGAGGA GAT G USP36 Ensembl:ENSG00000055483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1365450676 Functional Loss DEL dbSNP153 33..34 33 - - - 42335 RMVar_ID_42335 Human_SNP_ID_633807618 A-to-I Human chr17 - 78790676 78790676 78790676 GCCATTTTAAAATGAATGTGTTGGCCGGGCGCAGTGGCTCATGCTTGTAATTCCAGCACTTCAGG GCCATTTTAAAATGAATGTGTTGGCCGGGCGCGGTGGCTCATGCTTGTAATTCCAGCACTTCAGG T C USP36 Ensembl:ENSG00000055483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs936749026 Functional Loss SNV dbSNP153 33..33 33 - - - 42336 RMVar_ID_42336 Human_SNP_ID_633813146 A-to-I Human chr17 - 78807976 78807976 78807976 ATTCAGGCCAGGTGCTATGGCTCACACCTGTAATCCCAACACTTCTGGAGGCTGAGGCAGGTGGA ATTCAGGCCAGGTGCTATGGCTCACACCTGTAGTCCCAACACTTCTGGAGGCTGAGGCAGGTGGA T C USP36 Ensembl:ENSG00000055483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1274749877 Functional Loss SNV dbSNP153 33..33 33 - - - 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_187379,RMVar_hsa_circ_78898,RMVar_hsa_circ_367628,RMVar_hsa_circ_187380 42337 RMVar_ID_42337 Human_SNP_ID_633813147 A-to-I Human chr17 - 78807977 78807977 78807977 TATTCAGGCCAGGTGCTATGGCTCACACCTGTAATCCCAACACTTCTGGAGGCTGAGGCAGGTGG TATTCAGGCCAGGTGCTATGGCTCACACCTGTCATCCCAACACTTCTGGAGGCTGAGGCAGGTGG T G USP36 Ensembl:ENSG00000055483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs985710187 Functional Loss SNV dbSNP153 33..33 33 - - - 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_187379,RMVar_hsa_circ_78898,RMVar_hsa_circ_367628,RMVar_hsa_circ_187380 42338 RMVar_ID_42338 Human_SNP_ID_633813808 A-to-I Human chr17 - 78810426 78810426 78810426 AAAGCTAGCCAGGTTTAATGGCACGTGCCTGTATTCCCAGCTACTCAGGAGGCTGAGGTGGGAGG AAAGCTAGCCAGGTTTAATGGCACGTGCCTGTGTTCCCAGCTACTCAGGAGGCTGAGGTGGGAGG T C USP36 Ensembl:ENSG00000055483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs768352524 Functional Loss SNV dbSNP153 33..33 33 - - - 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_187379,RMVar_hsa_circ_78898,RMVar_hsa_circ_367628,RMVar_hsa_circ_187380 42339 RMVar_ID_42339 Human_SNP_ID_633821197 A-to-I Human chr17 - 78834972 78834972 78834972 ATATATACAAATATTATTTTTTTAGAGACAGTATCTTGCTCTGACACCCAGGCTGGAATGCAGTG ATATATACAAATATTATTTTTTTAGAGACAGTGTCTTGCTCTGACACCCAGGCTGGAATGCAGTG T C USP36 Ensembl:ENSG00000055483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946769117 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13184594 RMVar_hsa_circ_348349,RMVar_hsa_circ_367628,RMVar_hsa_circ_370974,RMVar_hsa_circ_187385,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_317289,RMVar_hsa_circ_60096,RMVar_hsa_circ_187391,RMVar_hsa_circ_187396,RMVar_hsa_circ_82685,RMVar_hsa_circ_324429,RMVar_hsa_circ_187397 42340 RMVar_ID_42340 Human_SNP_ID_633823924 A-to-I Human chr17 + 78843904 78843904 78843904 TCAAGCGATTATCGTGTCTCGGCCTCCAGAGTAGCTGGGATCACAGGTGCACGCCACCACACCCA TCAAGCGATTATCGTGTCTCGGCCTCCAGAGTGGCTGGGATCACAGGTGCACGCCACCACACCCA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1473567597 Functional Loss SNV dbSNP153 33..33 33 - - - 42341 RMVar_ID_42341 Human_SNP_ID_633827945 A-to-I Human chr17 - 78858661 78858661 78858661 AAAAAATTAGCAGGGTGTAGTGGTTCACACCTATAGTCCCAGCTATTCAGGAGACTGAGACGGGA AAAAAATTAGCAGGGTGTAGTGGTTCACACCTGTAGTCCCAGCTATTCAGGAGACTGAGACGGGA T C TIMP2 Ensembl:ENSG00000035862 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs916779150 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85266,RMVar_hsa_circ_87361,RMVar_hsa_circ_108052,RMVar_hsa_circ_90083,RMVar_hsa_circ_85973,RMVar_hsa_circ_187404,RMVar_hsa_circ_187406,RMVar_hsa_circ_187408,RMVar_hsa_circ_187407,RMVar_hsa_circ_187405,RMVar_hsa_circ_187410,RMVar_hsa_circ_110570,RMVar_hsa_circ_336767 42342 RMVar_ID_42342 Human_SNP_ID_633840561 A-to-I Human chr17 - 78903913 78903913 78903913 TCTAAAAAACAAACAAAAAACATATCTTGACAATGCCAGTCATCACTTTACCACAGACCTTAAGA TCTAAAAAACAAACAAAAAACATATCTTGACAGTGCCAGTCATCACTTTACCACAGACCTTAAGA T C TIMP2 Ensembl:ENSG00000035862 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1418518655 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108052,RMVar_hsa_circ_85973,RMVar_hsa_circ_187404,RMVar_hsa_circ_187405 42343 RMVar_ID_42343 Human_SNP_ID_633841244 A-to-I Human chr17 - 78906324 78906324 78906324 TTGCTCTGTCACTCAGGCTGGAGTGCAGTGGCATGATCTTAGCTCACTGCAGCCTCGAACTTCTG TTGCTCTGTCACTCAGGCTGGAGTGCAGTGGCCTGATCTTAGCTCACTGCAGCCTCGAACTTCTG T G TIMP2 Ensembl:ENSG00000035862 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042275323 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108052,RMVar_hsa_circ_85973,RMVar_hsa_circ_187404,RMVar_hsa_circ_187405 42344 RMVar_ID_42344 Human_SNP_ID_633866551 A-to-I Human chr17 - 78997271 78997271 78997271 TCGCAGTTATCGCAGACCTGGACACAGAGTCAAGGGCCCAAGAGGAAAACACCTGGTTCAGTTAC TCGCAGTTATCGCAGACCTGGACACAGAGTCAGGGGCCCAAGAGGAAAACACCTGGTTCAGTTAC T C CANT1 Ensembl:ENSG00000171302 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs755943793 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13184892,Human_RBP_ID_22443960,Human_RBP_ID_27260888,Human_RBP_ID_27458021 Human_Splice_Rec_1876556 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 42345 RMVar_ID_42345 Human_SNP_ID_634071790 A-to-I Human chr17 - 79753772 79753772 79753772 CACCTGACTGCAACCTCCACCTTCCAGGTTCAAACGTTTCTCGTGCCTCAGTGTCCCGAGTAGCT CACCTGACTGCAACCTCCACCTTCCAGGTTCAGACGTTTCTCGTGCCTCAGTGTCCCGAGTAGCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1555826173 Functional Loss SNV dbSNP153 33..33 33 - - - 42346 RMVar_ID_42346 Human_SNP_ID_634072096 A-to-I Human chr17 - 79755132 79755132 79755132 CAAGCTGGTGTTCAATGGCACAATCTTGGCTCACTGCAACCTCCACCTCCTGGGTTCAAGTGATC CAAGCTGGTGTTCAATGGCACAATCTTGGCTCCCTGCAACCTCCACCTCCTGGGTTCAAGTGATC T G HSALNG0119124 RNACentral:URS0000E9D7C9 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs781975127 Functional Loss SNV dbSNP153 33..33 33 - - - 42347 RMVar_ID_42347 Human_SNP_ID_634072138 A-to-I Human chr17 - 79755285 79755285 79755285 TTTGTACTTTTAGTAGAGACGGGGGTTTCACCATGTTGTCCAGACTGGTCTCGAACTCTTGACCT TTTGTACTTTTAGTAGAGACGGGGGTTTCACCGTGTTGTCCAGACTGGTCTCGAACTCTTGACCT T C HSALNG0119124 RNACentral:URS0000E9D7C9 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs372196761 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13185520 42348 RMVar_ID_42348 Human_SNP_ID_634072157 A-to-I Human chr17 - 79755362 79755362 79755362 GGGTTCAAGCAATTCTCCTGCCTCAGCCTCTCAAGTAGCTGGGATTACAGGTCCTGCCACCACGC GGGTTCAAGCAATTCTCCTGCCTCAGCCTCTCGAGTAGCTGGGATTACAGGTCCTGCCACCACGC T C HSALNG0119124 RNACentral:URS0000E9D7C9 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1345772760 Functional Loss SNV dbSNP153 33..33 33 - - - 42349 RMVar_ID_42349 Human_SNP_ID_634072280 A-to-I Human chr17 - 79755944 79755944 79755944 CCACTGCACTCCAGCCTGCACCACAAGCGTGAAACTCTGTCTCAAAAAAACAAAAACAAAAACAT CCACTGCACTCCAGCCTGCACCACAAGCGTGAGACTCTGTCTCAAAAAAACAAAAACAAAAACAT T C HSALNG0119124 RNACentral:URS0000E9D7C9 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1420014251 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27458093 42350 RMVar_ID_42350 Human_SNP_ID_634072283 A-to-I Human chr17 - 79755952 79755952 79755952 AGATGGCGCCACTGCACTCCAGCCTGCACCACAAGCGTGAAACTCTGTCTCAAAAAAACAAAAAC AGATGGCGCCACTGCACTCCAGCCTGCACCACTAGCGTGAAACTCTGTCTCAAAAAAACAAAAAC T A HSALNG0119124 RNACentral:URS0000E9D7C9 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1199114421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13185523,Human_RBP_ID_27458093 42351 RMVar_ID_42351 Human_SNP_ID_634072320 A-to-I Human chr17 - 79756081 79756081 79756081 GAAACCCCATCTCTACTAAAAATACAAAAATTAGTCAGGCGTGGTGGCGGGCACCTGTAACACCA GAAACCCCATCTCTACTAAAAATACAAAAATTGGTCAGGCGTGGTGGCGGGCACCTGTAACACCA T C HSALNG0119124 RNACentral:URS0000E9D7C9 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs546264483 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13185525 42352 RMVar_ID_42352 Human_SNP_ID_634074725 A-to-I Human chr17 - 79765378 79765378 79765378 TATTTTTAGTAGAGACTGGGTTTCACTGTGTTAGCCAGGATGGTCTCCATCTCCTGACCTTGTGA TATTTTTAGTAGAGACTGGGTTTCACTGTGTTTGCCAGGATGGTCTCCATCTCCTGACCTTGTGA T A HSALNG0119124 RNACentral:URS0000E9D7C9 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1222195131 Functional Loss SNV dbSNP153 33..33 33 - - - 42353 RMVar_ID_42353 Human_SNP_ID_634121532 A-to-I Human chr17 + 79923188 79923188 79923188 TCGCACAGGCTGGAGTGCAGTGACACGATCTCAGCTCACTGTAACCTCTGCCTCTCGGGTTCAAC TCGCACAGGCTGGAGTGCAGTGACACGATCTCGGCTCACTGTAACCTCTGCCTCTCGGGTTCAAC A G LINC01978 Ensembl:ENSG00000262188 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs186350257 Functional Loss SNV dbSNP153 33..33 33 - - - 42354 RMVar_ID_42354 Human_SNP_ID_634121533 A-to-I Human chr17 + 79923188 79923188 79923188 TCGCACAGGCTGGAGTGCAGTGACACGATCTCAGCTCACTGTAACCTCTGCCTCTCGGGTTCAAC TCGCACAGGCTGGAGTGCAGTGACACGATCTCTGCTCACTGTAACCTCTGCCTCTCGGGTTCAAC A T LINC01978 Ensembl:ENSG00000262188 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs186350257 Functional Loss SNV dbSNP153 33..33 33 - - - 42355 RMVar_ID_42355 Human_SNP_ID_634184710 A-to-I Human chr17 - 80138603 80138598 80138603 AACAGAGCAAGACCCTGTCTCAAACAAAACAAAACAACCCATCTTTTATAATCCTCATTGTGGTT AACAGAGCAAGACCCTGTCTCAAACAAAACAA_____CCCATCTTTTATAATCCTCATTGTGGTT GTTGTT G EIF4A3 Ensembl:ENSG00000141543 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs779699736 Functional Loss DEL dbSNP153 33..37 33 - - - RMVar_hsa_circ_17565,RMVar_hsa_circ_187458,RMVar_hsa_circ_344364,RMVar_hsa_circ_26147,RMVar_hsa_circ_107124,RMVar_hsa_circ_187461,RMVar_hsa_circ_83461,RMVar_hsa_circ_187462,RMVar_hsa_circ_345039,RMVar_hsa_circ_187464,RMVar_hsa_circ_55970 42356 RMVar_ID_42356 Human_SNP_ID_634184710 A-to-I Human chr17 - 80138602 80138598 80138603 ACAGAGCAAGACCCTGTCTCAAACAAAACAAAACAACCCATCTTTTATAATCCTCATTGTGGTTT ACAGAGCAAGACCCTGTCTCAAACAAAACAA_____CCCATCTTTTATAATCCTCATTGTGGTTT GTTGTT G EIF4A3 Ensembl:ENSG00000141543 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs779699736 Functional Loss DEL dbSNP153 32..36 33 - - - RMVar_hsa_circ_17565,RMVar_hsa_circ_187458,RMVar_hsa_circ_344364,RMVar_hsa_circ_26147,RMVar_hsa_circ_107124,RMVar_hsa_circ_187461,RMVar_hsa_circ_83461,RMVar_hsa_circ_187462,RMVar_hsa_circ_345039,RMVar_hsa_circ_187464,RMVar_hsa_circ_55970 42357 RMVar_ID_42357 Human_SNP_ID_634184712 A-to-I Human chr17 - 80138603 80138603 80138603 AACAGAGCAAGACCCTGTCTCAAACAAAACAAAACAACCCATCTTTTATAATCCTCATTGTGGTT AACAGAGCAAGACCCTGTCTCAAACAAAACAACACAACCCATCTTTTATAATCCTCATTGTGGTT T G EIF4A3 Ensembl:ENSG00000141543 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1296586290 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17565,RMVar_hsa_circ_187458,RMVar_hsa_circ_344364,RMVar_hsa_circ_26147,RMVar_hsa_circ_107124,RMVar_hsa_circ_187461,RMVar_hsa_circ_83461,RMVar_hsa_circ_187462,RMVar_hsa_circ_345039,RMVar_hsa_circ_187464,RMVar_hsa_circ_55970 42358 RMVar_ID_42358 Human_SNP_ID_634187876 A-to-I Human chr17 + 80148695 80148695 80148695 CTCCTGCCTCAGCCTCCCAAATAGCTGGGACTACAGACACGCGCCACCACGCCCAGCTAATTTTC CTCCTGCCTCAGCCTCCCAAATAGCTGGGACTGCAGACACGCGCCACCACGCCCAGCTAATTTTC A G lnc-CARD14-4 RNACentral:URS0000D5ADD6 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1189706739 Functional Loss SNV dbSNP153 33..33 33 - - - 42359 RMVar_ID_42359 Human_SNP_ID_634188175 A-to-I Human chr17 + 80149422 80149422 80149422 TGGTGAAACCCCATCTCTACTAAAAAAAAAATACAAAAATTAGCTGGCCGTGGTGACGGGTGTCT TGGTGAAACCCCATCTCTACTAAAAAAAAAATGCAAAAATTAGCTGGCCGTGGTGACGGGTGTCT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1473629527 Functional Loss SNV dbSNP153 33..33 33 - - - 42360 RMVar_ID_42360 Human_SNP_ID_634188176 A-to-I Human chr17 + 80149422 80149422 80149422 TGGTGAAACCCCATCTCTACTAAAAAAAAAATACAAAAATTAGCTGGCCGTGGTGACGGGTGTCT TGGTGAAACCCCATCTCTACTAAAAAAAAAATTCAAAAATTAGCTGGCCGTGGTGACGGGTGTCT A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1473629527 Functional Loss SNV dbSNP153 33..33 33 - - - 42361 RMVar_ID_42361 Human_SNP_ID_634188193 A-to-I Human chr17 + 80149467 80149467 80149467 GGCCGTGGTGACGGGTGTCTGTAGTCCCAGCTACTCTGGAGGCTGAGGCAGGAGAATCTCCTGAA GGCCGTGGTGACGGGTGTCTGTAGTCCCAGCTGCTCTGGAGGCTGAGGCAGGAGAATCTCCTGAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1339234497 Functional Loss SNV dbSNP153 33..33 33 - - - 42362 RMVar_ID_42362 Human_SNP_ID_634202338 A-to-I Human chr17 - 80201348 80201348 80201348 ATTCTGTGCTGCTGCGGGCTATACCGGGCCCTACAGGATGCTGAGTGGCATCCCTGGCCTTCACC ATTCTGTGCTGCTGCGGGCTATACCGGGCCCTTCAGGATGCTGAGTGGCATCCCTGGCCTTCACC T A AC087741.1 Ensembl:ENSG00000262580 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs113579819 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_3150531 42363 RMVar_ID_42363 Human_SNP_ID_634202339 A-to-I Human chr17 - 80201348 80201348 80201348 ATTCTGTGCTGCTGCGGGCTATACCGGGCCCTACAGGATGCTGAGTGGCATCCCTGGCCTTCACC ATTCTGTGCTGCTGCGGGCTATACCGGGCCCTGCAGGATGCTGAGTGGCATCCCTGGCCTTCACC T C AC087741.1 Ensembl:ENSG00000262580 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs113579819 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_3150531 42364 RMVar_ID_42364 Human_SNP_ID_634220516 A-to-I Human chr17 + 80259628 80259628 80259628 CGACTCACTGCAGCCTGGAGCTCCCTGGGCTCAAACGATCCTCTTGCCTCAGCCTCTTCAGGTGC CGACTCACTGCAGCCTGGAGCTCCCTGGGCTCGAACGATCCTCTTGCCTCAGCCTCTTCAGGTGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1242383453 Functional Loss SNV dbSNP153 33..33 33 - - - 42365 RMVar_ID_42365 Human_SNP_ID_634222886 A-to-I Human chr17 + 80267096 80267096 80267096 AAAATTAGCTGGGTGTGGTGGCTCATGCCTGTAATCCCAGCTTCTTGGGAGGCTGAGGCACAAGA AAAATTAGCTGGGTGTGGTGGCTCATGCCTGTGATCCCAGCTTCTTGGGAGGCTGAGGCACAAGA A G RNF213 Ensembl:ENSG00000173821 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs941381160 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40321,RMVar_hsa_circ_71953,RMVar_hsa_circ_337212,RMVar_hsa_circ_342254,RMVar_hsa_circ_346754,RMVar_hsa_circ_358711,RMVar_hsa_circ_338067,RMVar_hsa_circ_303270,RMVar_hsa_circ_308673,RMVar_hsa_circ_84809,RMVar_hsa_circ_54786,RMVar_hsa_circ_40661,RMVar_hsa_circ_187482,RMVar_hsa_circ_9447,RMVar_hsa_circ_187483,RMVar_hsa_circ_187481,RMVar_hsa_circ_378408 42366 RMVar_ID_42366 Human_SNP_ID_634222954 A-to-I Human chr17 + 80267330 80267330 80267330 AGGCATGGTGGCGTGTACCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAGAATCACTTG AGGCATGGTGGCGTGTACCTGTAGTCCCAGCTCCTCGGGAGGCTGAGGCAGGAGAGAATCACTTG A C RNF213 Ensembl:ENSG00000173821 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1408016816 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40321,RMVar_hsa_circ_71953,RMVar_hsa_circ_337212,RMVar_hsa_circ_342254,RMVar_hsa_circ_346754,RMVar_hsa_circ_358711,RMVar_hsa_circ_338067,RMVar_hsa_circ_303270,RMVar_hsa_circ_308673,RMVar_hsa_circ_84809,RMVar_hsa_circ_54786,RMVar_hsa_circ_40661,RMVar_hsa_circ_187482,RMVar_hsa_circ_9447,RMVar_hsa_circ_187483,RMVar_hsa_circ_187481,RMVar_hsa_circ_378408 42367 RMVar_ID_42367 Human_SNP_ID_634228909 A-to-I Human chr17 + 80285770 80285770 80285770 TCGGCTGACCGCAGCCTCTGCCTCCCGGGTTCAAGCAATTCTCCTGCTTCAGCCTCCCAAGTAGC TCGGCTGACCGCAGCCTCTGCCTCCCGGGTTCGAGCAATTCTCCTGCTTCAGCCTCCCAAGTAGC A G RNF213 Ensembl:ENSG00000173821 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1157514276 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42368 RMVar_ID_42368 Human_SNP_ID_634231185 A-to-I Human chr17 + 80292259 80292259 80292259 GGAGCCTGTCACCACCCCCAGCTAACTTTTGTATTTTTAGAGAGACAGGGTTTCACCATGTTGGA GGAGCCTGTCACCACCCCCAGCTAACTTTTGTGTTTTTAGAGAGACAGGGTTTCACCATGTTGGA A G RNF213 Ensembl:ENSG00000173821 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs992947411 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_74205 42369 RMVar_ID_42369 Human_SNP_ID_634231186 A-to-I Human chr17 + 80292265 80292264 80292266 TGTCACCACCCCCAGCTAACTTTTGTATTTTTAGAGAGACAGGGTTTCACCATGTTGGACCTTGA TGTCACCACCCCCAGCTAACTTTTGTATTTTT__AGAGACAGGGTTTCACCATGTTGGACCTTGA TAG T RNF213 Ensembl:ENSG00000173821 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1180474962 Functional Loss DEL dbSNP153 33..34 33 - - - 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_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_74205 42370 RMVar_ID_42370 Human_SNP_ID_634231187 A-to-I Human chr17 + 80292265 80292265 80292265 TGTCACCACCCCCAGCTAACTTTTGTATTTTTAGAGAGACAGGGTTTCACCATGTTGGACCTTGA TGTCACCACCCCCAGCTAACTTTTGTATTTTTGGAGAGACAGGGTTTCACCATGTTGGACCTTGA A G RNF213 Ensembl:ENSG00000173821 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs996172591 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_74205 42371 RMVar_ID_42371 Human_SNP_ID_634231214 A-to-I Human chr17 + 80292342 80292342 80292342 TGCCCTCCTCGACCTCCCGAAGTGTTGGGATTACAGGTGTAAGCCACTATGCCCAGCCAGAAAGG TGCCCTCCTCGACCTCCCGAAGTGTTGGGATTGCAGGTGTAAGCCACTATGCCCAGCCAGAAAGG A G RNF213 Ensembl:ENSG00000173821 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1349624330 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_74205 42372 RMVar_ID_42372 Human_SNP_ID_634236765 A-to-I Human chr17 + 80311858 80311845 80311858 AAAAAAAGATCACACACTTGGCTGGGTGTAGTAGCTCACACCTGTAATCCCAGCACTTTGGAAGG AAAAAAAGATCACACACTTG_____________GCTCACACCTGTAATCCCAGCACTTTGGAAGG GGCTGGGTGTAGTA G RNF213 Ensembl:ENSG00000173821 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1477132326 Functional Loss DEL dbSNP153 21..33 33 - - - RMVar_hsa_circ_40321,RMVar_hsa_circ_346754,RMVar_hsa_circ_338067,RMVar_hsa_circ_54786,RMVar_hsa_circ_40661,RMVar_hsa_circ_11022,RMVar_hsa_circ_56827,RMVar_hsa_circ_358836,RMVar_hsa_circ_339933,RMVar_hsa_circ_354181,RMVar_hsa_circ_351683,RMVar_hsa_circ_339060,RMVar_hsa_circ_69052,RMVar_hsa_circ_14933,RMVar_hsa_circ_65009,RMVar_hsa_circ_104520,RMVar_hsa_circ_127968,RMVar_hsa_circ_187489,RMVar_hsa_circ_55597,RMVar_hsa_circ_82497,RMVar_hsa_circ_187490,RMVar_hsa_circ_105979,RMVar_hsa_circ_71425,RMVar_hsa_circ_187492,RMVar_hsa_circ_17699,RMVar_hsa_circ_187493 42373 RMVar_ID_42373 Human_SNP_ID_634241051 A-to-I Human chr17 + 80321829 80321829 80321829 CACTGCGACACCTCCACCTCCTGGGTTCAAGCAATTCTCCTGCCTCAGTCTCTCGAGTAGCTGGG CACTGCGACACCTCCACCTCCTGGGTTCAAGCGATTCTCCTGCCTCAGTCTCTCGAGTAGCTGGG A G RNF213 Ensembl:ENSG00000173821 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1431534701 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7420,RMVar_hsa_circ_40321,RMVar_hsa_circ_54786,RMVar_hsa_circ_40661,RMVar_hsa_circ_56827,RMVar_hsa_circ_354181,RMVar_hsa_circ_339060,RMVar_hsa_circ_69052,RMVar_hsa_circ_14933,RMVar_hsa_circ_127968,RMVar_hsa_circ_82497,RMVar_hsa_circ_187490,RMVar_hsa_circ_105979,RMVar_hsa_circ_187492,RMVar_hsa_circ_17699,RMVar_hsa_circ_187493,RMVar_hsa_circ_87859,RMVar_hsa_circ_267164,RMVar_hsa_circ_120266,RMVar_hsa_circ_53717,RMVar_hsa_circ_59841,RMVar_hsa_circ_68675,RMVar_hsa_circ_187495,RMVar_hsa_circ_57756,RMVar_hsa_circ_266752,RMVar_hsa_circ_313635,RMVar_hsa_circ_31580,RMVar_hsa_circ_266998,RMVar_hsa_circ_265189,RMVar_hsa_circ_14983,RMVar_hsa_circ_61024,RMVar_hsa_circ_187496 42374 RMVar_ID_42374 Human_SNP_ID_634241065 A-to-I Human chr17 + 80321865 80321865 80321865 CTCCTGCCTCAGTCTCTCGAGTAGCTGGGACTACAGGCATGTGCCACCATGCCCAGCTAATTTTT CTCCTGCCTCAGTCTCTCGAGTAGCTGGGACTGCAGGCATGTGCCACCATGCCCAGCTAATTTTT A G RNF213 Ensembl:ENSG00000173821 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs991476187 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7420,RMVar_hsa_circ_40321,RMVar_hsa_circ_54786,RMVar_hsa_circ_40661,RMVar_hsa_circ_56827,RMVar_hsa_circ_354181,RMVar_hsa_circ_339060,RMVar_hsa_circ_69052,RMVar_hsa_circ_14933,RMVar_hsa_circ_127968,RMVar_hsa_circ_82497,RMVar_hsa_circ_187490,RMVar_hsa_circ_105979,RMVar_hsa_circ_187492,RMVar_hsa_circ_17699,RMVar_hsa_circ_187493,RMVar_hsa_circ_87859,RMVar_hsa_circ_267164,RMVar_hsa_circ_120266,RMVar_hsa_circ_53717,RMVar_hsa_circ_59841,RMVar_hsa_circ_68675,RMVar_hsa_circ_187495,RMVar_hsa_circ_57756,RMVar_hsa_circ_266752,RMVar_hsa_circ_313635,RMVar_hsa_circ_31580,RMVar_hsa_circ_266998,RMVar_hsa_circ_265189,RMVar_hsa_circ_14983,RMVar_hsa_circ_61024,RMVar_hsa_circ_187496 42375 RMVar_ID_42375 Human_SNP_ID_634243437 A-to-I Human chr17 + 80331236 80331236 80331236 TCTGCTTTTTGGGAATCCTGTGACATAAAACTACTCAGCTCTCAGTGTTGCCCACTGGGACCCTA TCTGCTTTTTGGGAATCCTGTGACATAAAACTGCTCAGCTCTCAGTGTTGCCCACTGGGACCCTA A G RNF213 Ensembl:ENSG00000173821 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6420491 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7420,RMVar_hsa_circ_40321,RMVar_hsa_circ_54786,RMVar_hsa_circ_40661,RMVar_hsa_circ_56827,RMVar_hsa_circ_339060,RMVar_hsa_circ_69052,RMVar_hsa_circ_14933,RMVar_hsa_circ_127968,RMVar_hsa_circ_82497,RMVar_hsa_circ_187490,RMVar_hsa_circ_105979,RMVar_hsa_circ_187492,RMVar_hsa_circ_187493,RMVar_hsa_circ_87859,RMVar_hsa_circ_267164,RMVar_hsa_circ_120266,RMVar_hsa_circ_53717,RMVar_hsa_circ_59841,RMVar_hsa_circ_68675,RMVar_hsa_circ_187495,RMVar_hsa_circ_57756,RMVar_hsa_circ_266752,RMVar_hsa_circ_313635,RMVar_hsa_circ_266998,RMVar_hsa_circ_265189,RMVar_hsa_circ_54503,RMVar_hsa_circ_61024,RMVar_hsa_circ_269830,RMVar_hsa_circ_187496,RMVar_hsa_circ_307608,RMVar_hsa_circ_104895,RMVar_hsa_circ_187499,RMVar_hsa_circ_187500,RMVar_hsa_circ_187498,RMVar_hsa_circ_346193,RMVar_hsa_circ_350432,RMVar_hsa_circ_364644,RMVar_hsa_circ_74704,RMVar_hsa_circ_187501,RMVar_hsa_circ_115031 42376 RMVar_ID_42376 Human_SNP_ID_634262301 A-to-I Human chr17 + 80390562 80390562 80390562 GGGACTACAGGCGTGTACCACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGACAGAGTTTCA GGGACTACAGGCGTGTACCACCATGCCTGGCTCATTTTTGTATTTTTAGTAGAGACAGAGTTTCA A C RNF213 Ensembl:ENSG00000173821 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1381081260 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266998,RMVar_hsa_circ_96925,RMVar_hsa_circ_187517 42377 RMVar_ID_42377 Human_SNP_ID_634269800 A-to-I Human chr17 + 80415982 80415982 80415982 GGAGTTGGCCGGGCGCGGTGGCTCACGCCTGCAATCCCAGCACTTTGGGAGGCTGAGGCGGGGGA GGAGTTGGCCGGGCGCGGTGGCTCACGCCTGCTATCCCAGCACTTTGGGAGGCTGAGGCGGGGGA A T ENDOV Ensembl:ENSG00000173818 Protein coding exon GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs753454379 Functional Loss SNV dbSNP153 33..33 33 - - - 42378 RMVar_ID_42378 Human_SNP_ID_634269818 A-to-I Human chr17 + 80416023 80416023 80416023 ACTTTGGGAGGCTGAGGCGGGGGAATCACCTGAGGTCGGGAGTTCGAGACCAGCCTGACCAACAT ACTTTGGGAGGCTGAGGCGGGGGAATCACCTGCGGTCGGGAGTTCGAGACCAGCCTGACCAACAT A C ENDOV Ensembl:ENSG00000173818 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1161827711 Functional Loss SNV dbSNP153 33..33 33 - - - 42379 RMVar_ID_42379 Human_SNP_ID_634269843 A-to-I Human chr17 + 80416086 80416086 80416086 ATGGAGAAACCCGGTCTCTACTAAAAATACAAAATTAGACGGGTGTGGTGGCATATACCTGTAAT ATGGAGAAACCCGGTCTCTACTAAAAATACAACATTAGACGGGTGTGGTGGCATATACCTGTAAT A C ENDOV Ensembl:ENSG00000173818 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1365579282 Functional Loss SNV dbSNP153 33..33 33 - - - 42380 RMVar_ID_42380 Human_SNP_ID_634270130 A-to-I Human chr17 + 80416843 80416843 80416843 ATAATCTTGGCTCACTGTCAAGATCTGATCTCAACCTCCTGGACTCAAGTGATCCTCCCACCTTA ATAATCTTGGCTCACTGTCAAGATCTGATCTCTACCTCCTGGACTCAAGTGATCCTCCCACCTTA A T ENDOV Ensembl:ENSG00000173818 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1260421252 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17566269,Human_RBP_ID_23753382 42381 RMVar_ID_42381 Human_SNP_ID_634270159 A-to-I Human chr17 + 80416955 80416955 80416955 TTTTTTATTTTTTGTAGAGACAGGATCTCACTATGTTGCCCAGGGTGGTCTCCAGCTCCTGGGCT TTTTTTATTTTTTGTAGAGACAGGATCTCACTGTGTTGCCCAGGGTGGTCTCCAGCTCCTGGGCT A G ENDOV Ensembl:ENSG00000173818 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs8065009 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1879154 GWAS_ID_4957,GWAS_ID_4958,GWAS_ID_4959,GWAS_ID_4960,GWAS_ID_4961,GWAS_ID_4962,GWAS_ID_4963,GWAS_ID_4964,GWAS_ID_4965,GWAS_ID_4966,GWAS_ID_4967,GWAS_ID_4968,GWAS_ID_4969,GWAS_ID_4970 42382 RMVar_ID_42382 Human_SNP_ID_634271307 A-to-I Human chr17 + 80420886 80420884 80420886 TTTAGTAAACACGGGGTTTCTCCATGTTGGTCAGGCTGGTCTTGAACTCCCAACCTCAGGTGATC TTTAGTAAACACGGGGTTTCTCCATGTTGGT__GGCTGGTCTTGAACTCCCAACCTCAGGTGATC TCA T ENDOV Ensembl:ENSG00000173818 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1209506546 Functional Loss DEL dbSNP153 32..33 33 - - - 42383 RMVar_ID_42383 Human_SNP_ID_634285532 A-to-I Human chr17 - 80470686 80470686 80470686 ATGAACCGAGGCCGTCGCCCCTGCACACGCACACGCACACAGCCTGGTTTTGTCCTCATGCACAC ATGAACCGAGGCCGTCGCCCCTGCACACGCACGCGCACACAGCCTGGTTTTGTCCTCATGCACAC T C NPTX1 Ensembl:ENSG00000171246 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1376901221 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_502293,Human_RBP_ID_17902489,Human_RBP_ID_20277750,Human_RBP_ID_23753503,Human_RBP_ID_27261453,Human_RBP_ID_27458486 Human_miRNA_ID_577269,Human_miRNA_ID_2206032 RMVar_hsa_circ_118545,RMVar_hsa_circ_187520 42384 RMVar_ID_42384 Human_SNP_ID_634307196 A-to-I Human chr17 + 80549451 80549451 80549451 CCTGCCGCAGCCTCCCGAGTAGCTGGGATTACAGGTGCCCACCACCATGCCTGGCCAATTTTTTT CCTGCCGCAGCCTCCCGAGTAGCTGGGATTACGGGTGCCCACCACCATGCCTGGCCAATTTTTTT A G RPTOR Ensembl:ENSG00000141564 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs894019397 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85423,RMVar_hsa_circ_115028,RMVar_hsa_circ_187521,RMVar_hsa_circ_187522 42385 RMVar_ID_42385 Human_SNP_ID_634308395 A-to-I Human chr17 + 80554623 80554623 80554623 AAAATTAGCCGGGCGAGGTGACGGGCGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA AAAATTAGCCGGGCGAGGTGACGGGCGCCTGTCGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA A C RPTOR Ensembl:ENSG00000141564 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1328667681 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85423,RMVar_hsa_circ_115028,RMVar_hsa_circ_187521,RMVar_hsa_circ_187522 42386 RMVar_ID_42386 Human_SNP_ID_634327934 A-to-I Human chr17 + 80632828 80632823 80632828 TATTTACTTGAAAATTTTTATTTTTGTGAGATAAGACCTTACTCTGTTGCCCAGGCTGGAGTGCA TATTTACTTGAAAATTTTTATTTTTGTG_____AGACCTTACTCTGTTGCCCAGGCTGGAGTGCA GAGATA G RPTOR Ensembl:ENSG00000141564 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1216750876 Functional Loss DEL dbSNP153 29..33 33 - - - Human_RBP_ID_8465422,Human_RBP_ID_13190446 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 42387 RMVar_ID_42387 Human_SNP_ID_634341040 A-to-I Human chr17 + 80682306 80682306 80682306 TTAAATTTTTTTGTAAAGTCAGGGGTCTCCCTATGTAACTCAGGCTGGTCTTGAACTCCTGGACT TTAAATTTTTTTGTAAAGTCAGGGGTCTCCCTCTGTAACTCAGGCTGGTCTTGAACTCCTGGACT A C RPTOR Ensembl:ENSG00000141564 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs957200831 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 42388 RMVar_ID_42388 Human_SNP_ID_634341041 A-to-I Human chr17 + 80682306 80682306 80682306 TTAAATTTTTTTGTAAAGTCAGGGGTCTCCCTATGTAACTCAGGCTGGTCTTGAACTCCTGGACT TTAAATTTTTTTGTAAAGTCAGGGGTCTCCCTGTGTAACTCAGGCTGGTCTTGAACTCCTGGACT A G RPTOR Ensembl:ENSG00000141564 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs957200831 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 42389 RMVar_ID_42389 Human_SNP_ID_634362380 A-to-I Human chr17 + 80759099 80759099 80759099 ACGCCTGGGCCAGATGTGGCAGTGCGTCCTGTAGTCCCAGCTGCTTGGAAGGCCGAGGCAGGAGG ACGCCTGGGCCAGATGTGGCAGTGCGTCCTGTGGTCCCAGCTGCTTGGAAGGCCGAGGCAGGAGG A G RPTOR Ensembl:ENSG00000141564 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1299781705 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13191559 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_93882,RMVar_hsa_circ_31754,RMVar_hsa_circ_187531,RMVar_hsa_circ_334118,RMVar_hsa_circ_19144,RMVar_hsa_circ_187536,RMVar_hsa_circ_102436,RMVar_hsa_circ_187537,RMVar_hsa_circ_340675 42390 RMVar_ID_42390 Human_SNP_ID_634364441 A-to-I Human chr17 + 80767191 80767191 80767191 GCCCAGGAGTTCAAGACCAGCCTGGGCAACATAGCAAAACCCCATCTCTACAAAATATAAAAATT GCCCAGGAGTTCAAGACCAGCCTGGGCAACATGGCAAAACCCCATCTCTACAAAATATAAAAATT A G RPTOR Ensembl:ENSG00000141564 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900936175 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_93882,RMVar_hsa_circ_31754,RMVar_hsa_circ_187531,RMVar_hsa_circ_334118,RMVar_hsa_circ_19144,RMVar_hsa_circ_187536,RMVar_hsa_circ_102436,RMVar_hsa_circ_187537,RMVar_hsa_circ_340675 42391 RMVar_ID_42391 Human_SNP_ID_634418018 A-to-I Human chr17 + 80954874 80954874 80954874 GGGAGGCGGAGGTTGCAGTGAGCCAAGATCACACCACTGCACTCCAGCCTGGGCAAAAGTGTGAG GGGAGGCGGAGGTTGCAGTGAGCCAAGATCACTCCACTGCACTCCAGCCTGGGCAAAAGTGTGAG A T RPTOR Ensembl:ENSG00000141564 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1171888681 Functional Loss SNV dbSNP153 33..33 33 - - - 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_187548,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_116660,RMVar_hsa_circ_77699,RMVar_hsa_circ_187553,RMVar_hsa_circ_187554,RMVar_hsa_circ_187552,RMVar_hsa_circ_330277 42392 RMVar_ID_42392 Human_SNP_ID_634433359 A-to-I Human chr17 + 81003047 81003047 81003047 TGGAACTCGGGCTCAAGCGATCCTCCCACCTCAGCCTCCTGAGTAGCTGGGACTACAGGTGTGTG TGGAACTCGGGCTCAAGCGATCCTCCCACCTCGGCCTCCTGAGTAGCTGGGACTACAGGTGTGTG A G CHMP6 Ensembl:ENSG00000176108 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs529541196 Functional Loss SNV dbSNP153 33..33 33 - - - 42393 RMVar_ID_42393 Human_SNP_ID_634517951 A-to-I Human chr17 - 81247784 81247784 81247784 CAGGCTGGAGTGCAGTGGTGTGATCACGGCTCACTGCAGCCTCGACCTCCTGGGCTCAAATGATC CAGGCTGGAGTGCAGTGGTGTGATCACGGCTCCCTGCAGCCTCGACCTCCTGGGCTCAAATGATC T G SLC38A10 Ensembl:ENSG00000157637 Protein coding intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1040093803 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42394 RMVar_ID_42394 Human_SNP_ID_634529280 A-to-I Human chr17 - 81284282 81284282 81284282 AATGCTGTGATCTCGGCTCACTGCAACCTCCCAGGTTTAAGCGATTCTCCTGCCTCAGCCTCCGA AATGCTGTGATCTCGGCTCACTGCAACCTCCCGGGTTTAAGCGATTCTCCTGCCTCAGCCTCCGA T C SLC38A10 Ensembl:ENSG00000157637 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1205228659 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125038,RMVar_hsa_circ_76394,RMVar_hsa_circ_187598,RMVar_hsa_circ_125698,RMVar_hsa_circ_187601,RMVar_hsa_circ_340994,RMVar_hsa_circ_290228,RMVar_hsa_circ_339696,RMVar_hsa_circ_187606,RMVar_hsa_circ_187605,RMVar_hsa_circ_47429,RMVar_hsa_circ_108875,RMVar_hsa_circ_283359,RMVar_hsa_circ_278595,RMVar_hsa_circ_187614,RMVar_hsa_circ_187613,RMVar_hsa_circ_187621,RMVar_hsa_circ_272150,RMVar_hsa_circ_187623,RMVar_hsa_circ_36091 42395 RMVar_ID_42395 Human_SNP_ID_634529294 A-to-I Human chr17 - 81284313 81284313 81284313 GAGTTTTGCTCTGTCACCCAGGCTGGAGTGCAATGCTGTGATCTCGGCTCACTGCAACCTCCCAG GAGTTTTGCTCTGTCACCCAGGCTGGAGTGCAGTGCTGTGATCTCGGCTCACTGCAACCTCCCAG T C SLC38A10 Ensembl:ENSG00000157637 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs558207205 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125038,RMVar_hsa_circ_76394,RMVar_hsa_circ_187598,RMVar_hsa_circ_125698,RMVar_hsa_circ_187601,RMVar_hsa_circ_340994,RMVar_hsa_circ_290228,RMVar_hsa_circ_339696,RMVar_hsa_circ_187606,RMVar_hsa_circ_187605,RMVar_hsa_circ_47429,RMVar_hsa_circ_108875,RMVar_hsa_circ_283359,RMVar_hsa_circ_278595,RMVar_hsa_circ_187614,RMVar_hsa_circ_187613,RMVar_hsa_circ_187621,RMVar_hsa_circ_272150,RMVar_hsa_circ_187623,RMVar_hsa_circ_36091 42396 RMVar_ID_42396 Human_SNP_ID_634556447 A-to-I Human chr17 - 81375360 81375360 81375360 TGAGGCAGGAGAATCGTTTGAACCCAGGAGGCAGAGTTTGCAGCGAGCCGAGATCGCGCCACTGC TGAGGCAGGAGAATCGTTTGAACCCAGGAGGCGGAGTTTGCAGCGAGCCGAGATCGCGCCACTGC T C AC110285.1 Ensembl:ENSG00000262223 lincRNA exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1314161147 Functional Loss SNV dbSNP153 33..33 33 - - - 42397 RMVar_ID_42397 Human_SNP_ID_634603192 A-to-I Human chr17 - 81511110 81511110 81511110 CACAGCATCACTAAGGGAGGGCTCTGTCCCCTAGGTATGGAATCTTGCGGCATCCACGAGACCAC CACAGCATCACTAAGGGAGGGCTCTGTCCCCTGGGTATGGAATCTTGCGGCATCCACGAGACCAC T C ACTG1 Ensembl:ENSG00000184009 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879982697 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19080401,Human_RBP_ID_22656967 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_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 42398 RMVar_ID_42398 Human_SNP_ID_634623712 A-to-I Human chr17 - 81560174 81560174 81560174 ACTTCAAGTGATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGACCCACTGCAC ACTTCAAGTGATCCACCCGCCTCGGCCTCCCAGAGTGCTGGGATTACAGGCGTGACCCACTGCAC T C NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs919982445 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22717644 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 42399 RMVar_ID_42399 Human_SNP_ID_634623770 A-to-I Human chr17 - 81560331 81560331 81560331 TCGGCTCACTGCAGGCTTCCCCTCCCGGGTTCATGGGATTCTCCTTCCTCAGCCTCCTGAGTAGC TCGGCTCACTGCAGGCTTCCCCTCCCGGGTTCGTGGGATTCTCCTTCCTCAGCCTCCTGAGTAGC T C NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1056747743 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13195378 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 42400 RMVar_ID_42400 Human_SNP_ID_634623834 A-to-I Human chr17 - 81560519 81560519 81560519 CATTTTTAGTAGAGACGGGGTTTCACCATGTTAGCCAGGATGGTCTCCATCTCTTGAATTTGTGA CATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGATGGTCTCCATCTCTTGAATTTGTGA T C NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs767857692 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42401 RMVar_ID_42401 Human_SNP_ID_634623862 A-to-I Human chr17 - 81560631 81560631 81560631 GCAACCTCGGTTCACTGCAACCTCCGCCTCCCAGGTTCACGCCATTCTCCTTCCTCAGCCTTCCT GCAACCTCGGTTCACTGCAACCTCCGCCTCCCGGGTTCACGCCATTCTCCTTCCTCAGCCTTCCT T C NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE38233;GSE100210;GSE105773;GSE105773;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;Glioblastoma cells,U87MG;Glioblastoma cells,U87MG;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,29724793,29724793,31158229,32596459,32596459 RNA-Seq:(High) rs1372983823 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23308940 Human_Splice_Rec_1881203 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 42402 RMVar_ID_42402 Human_SNP_ID_634624059 A-to-I Human chr17 - 81561229 81561229 81561229 ATGCAGGTCGGGCATGGTAGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGTGGAT ATGCAGGTCGGGCATGGTAGCTCACGCCTGTAGTCCCAGCACTTTGGGAGGCCGAGGCGGTGGAT T C NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE38233;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,32596459 RNA-Seq:(High) rs965646745 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42403 RMVar_ID_42403 Human_SNP_ID_634624251 A-to-I Human chr17 - 81562042 81562042 81562042 TTTAGTAGAGATGGGGTTTCACCATGTTGGTCAGGCTGGTCTGGAACTCCTGACCTCAGGTGATC TTTAGTAGAGATGGGGTTTCACCATGTTGGTCCGGCTGGTCTGGAACTCCTGACCTCAGGTGATC T G NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1024408450 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42404 RMVar_ID_42404 Human_SNP_ID_634624278 A-to-I Human chr17 - 81562143 81562143 81562143 ACTGCAACCTCCACGTCCTGGGTTCAAGTGATACTCCTGCCTCAGCCTCCCGAGTAGCTGGGACT ACTGCAACCTCCACGTCCTGGGTTCAAGTGATGCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACT T C NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1237707342 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_132046,Human_RBP_ID_13195476 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 42405 RMVar_ID_42405 Human_SNP_ID_634624284 A-to-I Human chr17 - 81562163 81562163 81562163 CAATCTCATGATCTCCACTTACTGCAACCTCCACGTCCTGGGTTCAAGTGATACTCCTGCCTCAG CAATCTCATGATCTCCACTTACTGCAACCTCCGCGTCCTGGGTTCAAGTGATACTCCTGCCTCAG T C NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1329544275 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13195476 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 42406 RMVar_ID_42406 Human_SNP_ID_634624287 A-to-I Human chr17 - 81562169 81562169 81562169 GCAGTGCAATCTCATGATCTCCACTTACTGCAACCTCCACGTCCTGGGTTCAAGTGATACTCCTG GCAGTGCAATCTCATGATCTCCACTTACTGCAGCCTCCACGTCCTGGGTTCAAGTGATACTCCTG T C NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs923088526 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13195476 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 42407 RMVar_ID_42407 Human_SNP_ID_634624304 A-to-I Human chr17 - 81562228 81562228 81562228 GGCCCTCATGGGTTGTTTTGTTTTGTTTTGAGACGGAATCTCACCCTGTCACCCAGGCTGCAGTG GGCCCTCATGGGTTGTTTTGTTTTGTTTTGAGGCGGAATCTCACCCTGTCACCCAGGCTGCAGTG T C NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs10445408 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1185006,Human_RBP_ID_3539558,Human_RBP_ID_6651294,Human_RBP_ID_13195476,Human_RBP_ID_23754675 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 42408 RMVar_ID_42408 Human_SNP_ID_634624349 A-to-I Human chr17 - 81562415 81562415 81562415 CCAGCCTCTGCCTCCTAAGTAGCTGGAATTACAGGTGGCTGCCACCACACCCAGCTAATTTTTTT CCAGCCTCTGCCTCCTAAGTAGCTGGAATTACGGGTGGCTGCCACCACACCCAGCTAATTTTTTT T C NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1433029707 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23172170 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 42409 RMVar_ID_42409 Human_SNP_ID_634624364 A-to-I Human chr17 - 81562470 81562470 81562470 CAGTAGTGTGATCTCAGCTCACTGCAGCCTCCACCTCCCGGGTTCAAGCCATTGTCCAGCCTCTG CAGTAGTGTGATCTCAGCTCACTGCAGCCTCCTCCTCCCGGGTTCAAGCCATTGTCCAGCCTCTG T A NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1328791432 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13195488,Human_RBP_ID_25330627 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 42410 RMVar_ID_42410 Human_SNP_ID_634624368 A-to-I Human chr17 - 81562482 81562482 81562482 CAGGCTGGAGTGCAGTAGTGTGATCTCAGCTCACTGCAGCCTCCACCTCCCGGGTTCAAGCCATT CAGGCTGGAGTGCAGTAGTGTGATCTCAGCTCGCTGCAGCCTCCACCTCCCGGGTTCAAGCCATT T C NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE47997;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,29129909,31158229,32596459 RNA-Seq:(High) rs1045965421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13195488 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 42411 RMVar_ID_42411 Human_SNP_ID_634624423 A-to-I Human chr17 - 81562697 81562697 81562697 TGGGCCCAAGCGATCCTCCCGCCTCAGTGCTGAGATTGCAGTGGTAAGCCACCATGTCCAGCCAA TGGGCCCAAGCGATCCTCCCGCCTCAGTGCTGTGATTGCAGTGGTAAGCCACCATGTCCAGCCAA T A NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1039505343 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1185007,Human_RBP_ID_13195509,Human_RBP_ID_18711508 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 42412 RMVar_ID_42412 Human_SNP_ID_634624424 A-to-I Human chr17 - 81562697 81562697 81562697 TGGGCCCAAGCGATCCTCCCGCCTCAGTGCTGAGATTGCAGTGGTAAGCCACCATGTCCAGCCAA TGGGCCCAAGCGATCCTCCCGCCTCAGTGCTGGGATTGCAGTGGTAAGCCACCATGTCCAGCCAA T C NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1039505343 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1185007,Human_RBP_ID_13195509,Human_RBP_ID_18711508 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 42413 RMVar_ID_42413 Human_SNP_ID_634624444 A-to-I Human chr17 - 81562756 81562756 81562756 TTTTAAATTTGTTGTAGAGATGAGGTCTCACTATGTTGCCCAGGCTGGTCTTGAACTCTTGGGCC TTTTAAATTTGTTGTAGAGATGAGGTCTCACTGTGTTGCCCAGGCTGGTCTTGAACTCTTGGGCC T C NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1046038706 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42414 RMVar_ID_42414 Human_SNP_ID_634624446 A-to-I Human chr17 - 81562759 81562759 81562759 ATTTTTTAAATTTGTTGTAGAGATGAGGTCTCACTATGTTGCCCAGGCTGGTCTTGAACTCTTGG ATTTTTTAAATTTGTTGTAGAGATGAGGTCTCGCTATGTTGCCCAGGCTGGTCTTGAACTCTTGG T C NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs575162405 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42415 RMVar_ID_42415 Human_SNP_ID_634624449 A-to-I Human chr17 - 81562773 81562773 81562773 ACCATCCCTGGCTGATTTTTTAAATTTGTTGTAGAGATGAGGTCTCACTATGTTGCCCAGGCTGG ACCATCCCTGGCTGATTTTTTAAATTTGTTGTGGAGATGAGGTCTCACTATGTTGCCCAGGCTGG T C NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1258821072 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13195514 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 42416 RMVar_ID_42416 Human_SNP_ID_634624457 A-to-I Human chr17 - 81562818 81562818 81562818 CTCCCGCCTCAGCCTCCTGAGCAGCTGGGACTACAAGCATGTGCCACCATCCCTGGCTGATTTTT CTCCCGCCTCAGCCTCCTGAGCAGCTGGGACTGCAAGCATGTGCCACCATCCCTGGCTGATTTTT T C NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE47997;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,29129909,31158229,32596459 RNA-Seq:(High) rs887965701 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23172172 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 42417 RMVar_ID_42417 Human_SNP_ID_634624479 A-to-I Human chr17 - 81562916 81562916 81562916 CTTTTTTTTTTGAGACAGGTTCTCACTCTGTCACCCAGGCTGAAGTGCAGTGGCATTTGAGGTCA CTTTTTTTTTTGAGACAGGTTCTCACTCTGTCTCCCAGGCTGAAGTGCAGTGGCATTTGAGGTCA T A NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs149217864 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13195519 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 42418 RMVar_ID_42418 Human_SNP_ID_634624482 A-to-I Human chr17 - 81562924 81562920 81562924 CCCCCCTCCTTTTTTTTTTGAGACAGGTTCTCACTCTGTCACCCAGGCTGAAGTGCAGTGGCATT CCCCCCTCCTTTTTTTTTTGAGACAGGTTCTC____TGTCACCCAGGCTGAAGTGCAGTGGCATT AGAGT A NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE47997;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 K562 cells&HepG2 cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 23474544,29129909,31158229 RNA-Seq:(High) rs1234666177 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_13195519 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 42419 RMVar_ID_42419 Human_SNP_ID_634624520 A-to-I Human chr17 - 81563006 81563006 81563006 TAGGCTCAAGTGATCTTCCTGCCTTGGTTCCCAAAGTGCTGAGATTACAGCTGTGAGCCACTGCA TAGGCTCAAGTGATCTTCCTGCCTTGGTTCCCGAAGTGCTGAGATTACAGCTGTGAGCCACTGCA T C NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs1420831005 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13195524 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 42420 RMVar_ID_42420 Human_SNP_ID_634624586 A-to-I Human chr17 - 81563186 81563186 81563186 CCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGACCCAGGAAGCGTAGGTTG CCTGTAATCCCAGCTACTCAGGAGGCTGAGGCTGGAGAATCACTTGACCCAGGAAGCGTAGGTTG T A NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE47997;GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,29129909,32596459 RNA-Seq:(High) rs1240212673 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42421 RMVar_ID_42421 Human_SNP_ID_634624588 A-to-I Human chr17 - 81563203 81563203 81563203 GGGCATGGTGGCGAGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAC GGGCATGGTGGCGAGCGCCTGTAATCCCAGCTGCTCAGGAGGCTGAGGCAGGAGAATCACTTGAC T C NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1457322954 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13195530,Human_RBP_ID_23754682 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 42422 RMVar_ID_42422 Human_SNP_ID_634624611 A-to-I Human chr17 - 81563310 81563310 81563310 CCAGCACTTTGGGAGGCTGAGGCAGGTGGATCACAACGTCAAGGGATTGAGACCATCCTGGCCAA CCAGCACTTTGGGAGGCTGAGGCAGGTGGATCTCAACGTCAAGGGATTGAGACCATCCTGGCCAA T A NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs560789351 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13195534,Human_RBP_ID_25330639 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 42423 RMVar_ID_42423 Human_SNP_ID_634624612 A-to-I Human chr17 - 81563310 81563310 81563310 CCAGCACTTTGGGAGGCTGAGGCAGGTGGATCACAACGTCAAGGGATTGAGACCATCCTGGCCAA CCAGCACTTTGGGAGGCTGAGGCAGGTGGATCGCAACGTCAAGGGATTGAGACCATCCTGGCCAA T C NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs560789351 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13195534,Human_RBP_ID_25330639 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 42424 RMVar_ID_42424 Human_SNP_ID_634624656 A-to-I Human chr17 - 81563454 81563454 81563454 GCGATCCTCCTGCATCAGCTTTCGGAGTACCTAGGAGTATAAACATGAGCCACTACACCCAACTA GCGATCCTCCTGCATCAGCTTTCGGAGTACCTGGGAGTATAAACATGAGCCACTACACCCAACTA T C NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1463659070 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8465974,Human_RBP_ID_13195544 Human_Splice_Rec_1881219 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 42425 RMVar_ID_42425 Human_SNP_ID_634624679 A-to-I Human chr17 - 81563556 81563556 81563556 CTTTTTTGTTTCCCTTTTAGAGACAGGGTTTCACTCTGTTGCCTAGGCTGGAGTGCAGTGGAGTG CTTTTTTGTTTCCCTTTTAGAGACAGGGTTTCCCTCTGTTGCCTAGGCTGGAGTGCAGTGGAGTG T G NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1449076839 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13195553,Human_RBP_ID_23754684,Human_RBP_ID_25330644 Human_Splice_Rec_1881218 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 42426 RMVar_ID_42426 Human_SNP_ID_634624714 A-to-I Human chr17 - 81563671 81563671 81563671 CCTCAAGCATTCCTTGCACCTCAGCCTCACAAAGTCCTGAGATTATACCTGGGAGCCACTGCACC CCTCAAGCATTCCTTGCACCTCAGCCTCACAAGGTCCTGAGATTATACCTGGGAGCCACTGCACC T C NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444318605 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13195559 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 42427 RMVar_ID_42427 Human_SNP_ID_634624793 A-to-I Human chr17 - 81563959 81563959 81563959 CCCCTCCCTCAGCCTCCCGAGTAGCTGGGATTACAGATGTGTACCACCACACCTGGCGTTGCCAT CCCCTCCCTCAGCCTCCCGAGTAGCTGGGATTGCAGATGTGTACCACCACACCTGGCGTTGCCAT T C NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE38233;GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,32596459 RNA-Seq:(High) rs1266626845 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9881641,Human_RBP_ID_23754695 Human_Splice_Rec_1881188,Human_Splice_Rec_1881189 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 42428 RMVar_ID_42428 Human_SNP_ID_634624806 A-to-I Human chr17 - 81563994 81563994 81563994 TCACTGCAAACTCTGCCTCCTGGGTTGAAGCAATTCCCCTCCCTCAGCCTCCCGAGTAGCTGGGA TCACTGCAAACTCTGCCTCCTGGGTTGAAGCAGTTCCCCTCCCTCAGCCTCCCGAGTAGCTGGGA T C NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,31158229,32596459 RNA-Seq:(High) rs1005724448 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23754696 Human_Splice_Rec_1881189 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 42429 RMVar_ID_42429 Human_SNP_ID_634624816 A-to-I Human chr17 - 81564034 81564034 81564034 CCCTGTCTCCCAGGCTGGAGTGCAGTGGCGCAATCTTAGCTCACTGCAAACTCTGCCTCCTGGGT CCCTGTCTCCCAGGCTGGAGTGCAGTGGCGCAGTCTTAGCTCACTGCAAACTCTGCCTCCTGGGT T C NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs900470132 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5648718,Human_RBP_ID_13195580,Human_RBP_ID_23754699 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 42430 RMVar_ID_42430 Human_SNP_ID_634625037 A-to-I Human chr17 - 81564545 81564545 81564545 GACCTTGTGATCTGCTTGCCTCTGCCTCCCAGAGTGTTGGGATTACAGGTGTGAGCCACCACGCC GACCTTGTGATCTGCTTGCCTCTGCCTCCCAGTGTGTTGGGATTACAGGTGTGAGCCACCACGCC T A NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1264990588 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3539567,Human_RBP_ID_13195624,Human_RBP_ID_23754725 RMVar_hsa_circ_107869,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_109492,RMVar_hsa_circ_93822,RMVar_hsa_circ_99888,RMVar_hsa_circ_102533,RMVar_hsa_circ_105515,RMVar_hsa_circ_100035,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_187671,RMVar_hsa_circ_77509,RMVar_hsa_circ_187672,RMVar_hsa_circ_187670,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_187658 42431 RMVar_ID_42431 Human_SNP_ID_634625090 A-to-I Human chr17 - 81564731 81564729 81564731 CAGGCTGGAGTGTGGTGGCGTGATCTTGCCTCACTGCAACCTCCACCTCCTGGGTTCAAACGATT CAGGCTGGAGTGTGGTGGCGTGATCTTGCCTC__TGCAACCTCCACCTCCTGGGTTCAAACGATT AGT A NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1196884605 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_107869,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_109492,RMVar_hsa_circ_93822,RMVar_hsa_circ_99888,RMVar_hsa_circ_102533,RMVar_hsa_circ_105515,RMVar_hsa_circ_100035,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_187671,RMVar_hsa_circ_77509,RMVar_hsa_circ_187672,RMVar_hsa_circ_187670,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_187658 42432 RMVar_ID_42432 Human_SNP_ID_634628999 A-to-I Human chr17 - 81579124 81579124 81579124 AGTAATCCACCTGCCTTGCCTCCCAAAGTGCTAGAACTACAGGCGTGAGCCACCACGCTAAACAG AGTAATCCACCTGCCTTGCCTCCCAAAGTGCTGGAACTACAGGCGTGAGCCACCACGCTAAACAG T C NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1190213518 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42433 RMVar_ID_42433 Human_SNP_ID_634629924 A-to-I Human chr17 - 81582462 81582462 81582462 AGGAGTTCACGGCTGCAGTGAGCTATGATTGTACCACTGTACTCCAGCCTGGGCGACAGAACAAG AGGAGTTCACGGCTGCAGTGAGCTATGATTGTGCCACTGTACTCCAGCCTGGGCGACAGAACAAG T C NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560471073 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25347852 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 42434 RMVar_ID_42434 Human_SNP_ID_634629957 A-to-I Human chr17 - 81582602 81582598 81582603 GCTCAGGAAGTCGAGGCCAGTCTGTGTGACATAGCAAGACCTCATTTCTACAACAACAAAAAAAA GCTCAGGAAGTCGAGGCCAGTCTGTGTGACA_____AGACCTCATTTCTACAACAACAAAAAAAA TTGCTA T NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1190114052 Functional Loss DEL dbSNP153 32..36 33 - - - Human_RBP_ID_13196286 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 42435 RMVar_ID_42435 Human_SNP_ID_634631105 A-to-I Human chr17 - 81586574 81586574 81586574 AGACAGTTTTGCTCTGTTACCCAGGCTGGAGTACAGTGGCGCGATCTCGGCCCACTGCAGCCTCC AGACAGTTTTGCTCTGTTACCCAGGCTGGAGTGCAGTGGCGCGATCTCGGCCCACTGCAGCCTCC T C NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs976121945 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13196458 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 42436 RMVar_ID_42436 Human_SNP_ID_634638361 A-to-I Human chr17 - 81611198 81611198 81611198 CTCCTGCCTCAGCCTCCCTGGTTCCTGGCATTACAGGTGCTTGCCACCACGTCCGGCTAATTTTT CTCCTGCCTCAGCCTCCCTGGTTCCTGGCATTGCAGGTGCTTGCCACCACGTCCGGCTAATTTTT T C NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1230948200 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42437 RMVar_ID_42437 Human_SNP_ID_634638391 A-to-I Human chr17 - 81611312 81611312 81611312 AACTATTTTATTTATTTATTTATTTGAGTGGAATTTCACTCTCGTCTCCCAGGCTGGAGTGCAGT AACTATTTTATTTATTTATTTATTTGAGTGGAGTTTCACTCTCGTCTCCCAGGCTGGAGTGCAGT T C NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs972341080 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42438 RMVar_ID_42438 Human_SNP_ID_634638455 A-to-I Human chr17 - 81611510 81611506 81611511 TCCCGTCTCTACTAAAAATACAAAAATTAGCCAGGCATGGTGGTGTGCACCTGTAGTCCCAGCTA TCCCGTCTCTACTAAAAATACAAAAATTAGC_____ATGGTGGTGTGCACCTGTAGTCCCAGCTA TGCCTG T NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1483425314 Functional Loss DEL dbSNP153 32..36 33 - - - 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 42439 RMVar_ID_42439 Human_SNP_ID_634638458 A-to-I Human chr17 - 81611523 81611523 81611523 CAATATGGTGAAATCCCGTCTCTACTAAAAATACAAAAATTAGCCAGGCATGGTGGTGTGCACCT CAATATGGTGAAATCCCGTCTCTACTAAAAATGCAAAAATTAGCCAGGCATGGTGGTGTGCACCT T C NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1244742616 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42440 RMVar_ID_42440 Human_SNP_ID_634644628 A-to-I Human chr17 - 81630432 81630432 81630432 AAAAAAAAAAATTAACCTGGTGTGGTGGTGCAAGCCTGTGGTTCCAGCTCTCGGGAGGCTGAGGT AAAAAAAAAAATTAACCTGGTGTGGTGGTGCAGGCCTGTGGTTCCAGCTCTCGGGAGGCTGAGGT T C NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs758725881 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42441 RMVar_ID_42441 Human_SNP_ID_634644751 A-to-I Human chr17 - 81630820 81630820 81630820 AATGCTGGAGTGCAGTGGCACCATCTTGGCTCACTGTAGCCTCGACCTCCCTGGTTTAAGTGATC AATGCTGGAGTGCAGTGGCACCATCTTGGCTCGCTGTAGCCTCGACCTCCCTGGTTTAAGTGATC T C NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1364149739 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42442 RMVar_ID_42442 Human_SNP_ID_634644822 A-to-I Human chr17 - 81631051 81631051 81631051 CTCCTGCCTCAGCCTCCCGGGTAGCTGGGATTACAGGTGCCCGCCACCACGCCCAGCTAATTTTT CTCCTGCCTCAGCCTCCCGGGTAGCTGGGATTTCAGGTGCCCGCCACCACGCCCAGCTAATTTTT T A NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs981098451 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42443 RMVar_ID_42443 Human_SNP_ID_634645200 A-to-I Human chr17 - 81631891 81631890 81631892 GGAGGCTGAGGCAGGAGAATCACTTGAACTCAAGAGGCAGAGGTTGCAGTGAGCCAAGATTGCGC GGAGGCTGAGGCAGGAGAATCACTTGAACTC__GAGGCAGAGGTTGCAGTGAGCCAAGATTGCGC CTT C NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1293939856 Functional Loss DEL dbSNP153 32..33 33 - - - 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 42444 RMVar_ID_42444 Human_SNP_ID_634645460 A-to-I Human chr17 - 81632941 81632941 81632941 TATTTTTAGTAGAGATGGGGTTTCACCGTGTTAGCCAGGATGGTCTCAATCTCCTGACTTAAAAG TATTTTTAGTAGAGATGGGGTTTCACCGTGTTGGCCAGGATGGTCTCAATCTCCTGACTTAAAAG T C NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs974748971 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42445 RMVar_ID_42445 Human_SNP_ID_634645482 A-to-I Human chr17 - 81633008 81633008 81633008 CTCCTACCTCAGCCTCCCAAGTAGCTGGGACTACAGGCGCCCTCCACCACGCCTGGCTAATGTTT CTCCTACCTCAGCCTCCCAAGTAGCTGGGACTGCAGGCGCCCTCCACCACGCCTGGCTAATGTTT T C NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs763707657 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42446 RMVar_ID_42446 Human_SNP_ID_634646057 A-to-I Human chr17 - 81634872 81634872 81634872 TGACTCCTTTGAAAAATAAAATGTGGCCATGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGG TGACTCCTTTGAAAAATAAAATGTGGCCATGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG T C NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1229384509 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42447 RMVar_ID_42447 Human_SNP_ID_634646072 A-to-I Human chr17 - 81634940 81634940 81634940 TCCTACCTTGGGGTCCCAAAATTGCTAGGATTACAGTCCTGAGCTACCATGCCCGGCCAAGAAAC TCCTACCTTGGGGTCCCAAAATTGCTAGGATTGCAGTCCTGAGCTACCATGCCCGGCCAAGAAAC T C NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs146076835 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17567147 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 42448 RMVar_ID_42448 Human_SNP_ID_634646074 A-to-I Human chr17 - 81634946 81634946 81634946 GGATCCTCCTACCTTGGGGTCCCAAAATTGCTAGGATTACAGTCCTGAGCTACCATGCCCGGCCA GGATCCTCCTACCTTGGGGTCCCAAAATTGCTGGGATTACAGTCCTGAGCTACCATGCCCGGCCA T C NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs909535256 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17567147 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 42449 RMVar_ID_42449 Human_SNP_ID_634646170 A-to-I Human chr17 - 81635231 81635231 81635231 GGGTTCAAGAAATTCTCCTGCCTCAGCCGAGTAGCTGGGGTTGCAGGTGCTCGCCAACACGCATG GGGTTCAAGAAATTCTCCTGCCTCAGCCGAGTCGCTGGGGTTGCAGGTGCTCGCCAACACGCATG T G NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1006429046 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42450 RMVar_ID_42450 Human_SNP_ID_634647090 A-to-I Human chr17 + 81637873 81637873 81637873 GGAGAATCTCTTGAAGCGAAGAGGCGGAGGTTAGAATGAACTGAGTTGGTGCCACTGCACTCCAG GGAGAATCTCTTGAAGCGAAGAGGCGGAGGTTGGAATGAACTGAGTTGGTGCCACTGCACTCCAG A G TSPAN10 Ensembl:ENSG00000182612 Protein coding exon GSE38233;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,32596459 RNA-Seq:(High) rs1183849723 Functional Loss SNV dbSNP153 33..33 33 - - - 42451 RMVar_ID_42451 Human_SNP_ID_634647264 A-to-I Human chr17 + 81638428 81638428 81638428 TCCAGTGATTCTCCTGCCTCAGCCTCCCGGGTAGCTGGGACTACAGGCGCACACTACCATGCCTG TCCAGTGATTCTCCTGCCTCAGCCTCCCGGGTGGCTGGGACTACAGGCGCACACTACCATGCCTG A G TSPAN10 Ensembl:ENSG00000182612 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031756159 Functional Loss SNV dbSNP153 33..33 33 - - - 42452 RMVar_ID_42452 Human_SNP_ID_634660484 A-to-I Human chr17 - 81679121 81679121 81679121 GAGACTGGAGCACAGTGGTGGGATCACAGCTCACTGCAGCCTCAACCTCCCAAGCTCAGTCAATC GAGACTGGAGCACAGTGGTGGGATCACAGCTCGCTGCAGCCTCAACCTCCCAAGCTCAGTCAATC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1261221255 Functional Loss SNV dbSNP153 33..33 33 - - - 42453 RMVar_ID_42453 Human_SNP_ID_634660633 A-to-I Human chr17 - 81679647 81679647 81679647 ATCTCGGCGACTCACTGCAACCTCTGCCACCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTG ATCTCGGCGACTCACTGCAACCTCTGCCACCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973076004 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13198296 42454 RMVar_ID_42454 Human_SNP_ID_634661175 A-to-I Human chr17 - 81681307 81681307 81681307 ATCTCAGCTACTTGGGAGGCTGAGACAGGAGAATCCCTTGAACCTGGGAGGTGGAGGTTGCAGTG ATCTCAGCTACTTGGGAGGCTGAGACAGGAGACTCCCTTGAACCTGGGAGGTGGAGGTTGCAGTG T G ARL16 Ensembl:ENSG00000214087 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs577437579 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26460015,Human_RBP_ID_26814124 42455 RMVar_ID_42455 Human_SNP_ID_634661177 A-to-I Human chr17 - 81681313 81681313 81681313 CCTGTAATCTCAGCTACTTGGGAGGCTGAGACAGGAGAATCCCTTGAACCTGGGAGGTGGAGGTT CCTGTAATCTCAGCTACTTGGGAGGCTGAGACGGGAGAATCCCTTGAACCTGGGAGGTGGAGGTT T C ARL16 Ensembl:ENSG00000214087 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs562727213 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26460015,Human_RBP_ID_26814124 42456 RMVar_ID_42456 Human_SNP_ID_634661218 A-to-I Human chr17 - 81681480 81681480 81681480 AGTGTCCCCAGGGGCTAGGCATGGTGGCTCACACCTGTAATCCCAGCACTTTGAGAGGCCGAGGC AGTGTCCCCAGGGGCTAGGCATGGTGGCTCACCCCTGTAATCCCAGCACTTTGAGAGGCCGAGGC T G ARL16 Ensembl:ENSG00000214087 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs570848748 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_502638,Human_RBP_ID_17902845 Human_miRNA_ID_55938,Human_miRNA_ID_63489,Human_miRNA_ID_386084,Human_miRNA_ID_562753,Human_miRNA_ID_570094,Human_miRNA_ID_770235,Human_miRNA_ID_775112,Human_miRNA_ID_779951,Human_miRNA_ID_784818,Human_miRNA_ID_1106137,Human_miRNA_ID_1110960,Human_miRNA_ID_1357690,Human_miRNA_ID_1511671,Human_miRNA_ID_1567054,Human_miRNA_ID_1572729,Human_miRNA_ID_1588176,Human_miRNA_ID_1599318,Human_miRNA_ID_1608772,Human_miRNA_ID_1613687,Human_miRNA_ID_1621169,Human_miRNA_ID_1637286,Human_miRNA_ID_1685455,Human_miRNA_ID_1738374 42457 RMVar_ID_42457 Human_SNP_ID_634668397 A-to-I Human chr17 + 81699591 81699590 81699591 GGGATTACAGGCGCCTGCCACCATGCCCAGCTAGTTTTTGTATTTTTATTAGAGACAGGGTTTTA GGGATTACAGGCGCCTGCCACCATGCCCAGCT_GTTTTTGTATTTTTATTAGAGACAGGGTTTTA TA T HGS Ensembl:ENSG00000185359 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1049596292 Functional Loss DEL dbSNP153 33..33 33 - - - 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 42458 RMVar_ID_42458 Human_SNP_ID_634668408 A-to-I Human chr17 - 81699622 81699622 81699622 CAGGAGTTCGAGACCAGGCTGTCTAACATAGTAAAACCCTGTCTCTAATAAAAATACAAAAACTA CAGGAGTTCGAGACCAGGCTGTCTAACATAGTGAAACCCTGTCTCTAATAAAAATACAAAAACTA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs566017464 Functional Loss SNV dbSNP153 33..33 33 - - - 42459 RMVar_ID_42459 Human_SNP_ID_634668409 A-to-I Human chr17 + 81699626 81699626 81699626 TTTTGTATTTTTATTAGAGACAGGGTTTTACTATGTTAGACAGCCTGGTCTCGAACTCCTGCCAT TTTTGTATTTTTATTAGAGACAGGGTTTTACTCTGTTAGACAGCCTGGTCTCGAACTCCTGCCAT A C HGS Ensembl:ENSG00000185359 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1205485809 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42460 RMVar_ID_42460 Human_SNP_ID_634668410 A-to-I Human chr17 + 81699626 81699626 81699626 TTTTGTATTTTTATTAGAGACAGGGTTTTACTATGTTAGACAGCCTGGTCTCGAACTCCTGCCAT TTTTGTATTTTTATTAGAGACAGGGTTTTACTGTGTTAGACAGCCTGGTCTCGAACTCCTGCCAT A G HGS Ensembl:ENSG00000185359 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1205485809 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42461 RMVar_ID_42461 Human_SNP_ID_634668479 A-to-I Human chr17 + 81699817 81699817 81699817 GAAAACTCCTGGCCGGGCGGTGGCTCACGCCTATAATCCCAGCACTTCGGGAGGCCGAGGCGGGT GAAAACTCCTGGCCGGGCGGTGGCTCACGCCTGTAATCCCAGCACTTCGGGAGGCCGAGGCGGGT A G HGS Ensembl:ENSG00000185359 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1376742990 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42462 RMVar_ID_42462 Human_SNP_ID_634668512 A-to-I Human chr17 + 81699891 81699891 81699891 GAGGTCAGGAGTTTGACACCAGCCTGACCAACATGGTGAAACCCGTCTCTCCTAAAAATACAAAA GAGGTCAGGAGTTTGACACCAGCCTGACCAACGTGGTGAAACCCGTCTCTCCTAAAAATACAAAA A G HGS Ensembl:ENSG00000185359 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1401808892 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42463 RMVar_ID_42463 Human_SNP_ID_634668558 A-to-I Human chr17 + 81700007 81700007 81700007 TGAGGCAGGAGAATTGCTTCAACCCAGGAAGCAGAGGTTGCAGTGAGCTGAGATCGCGCCACTGC TGAGGCAGGAGAATTGCTTCAACCCAGGAAGCGGAGGTTGCAGTGAGCTGAGATCGCGCCACTGC A G HGS Ensembl:ENSG00000185359 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs905941346 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42464 RMVar_ID_42464 Human_SNP_ID_634670632 A-to-I Human chr17 + 81704985 81704985 81704985 GGCTGGGCGTGGTGGCTCACGCCTGTAATCCCAGCGCTTCGGGAGGCCGAGACGGGTGGATCACT GGCTGGGCGTGGTGGCTCACGCCTGTAATCCCGGCGCTTCGGGAGGCCGAGACGGGTGGATCACT A G MRPL12,AC139530.2 Ensembl:ENSG00000262814,Ensembl:ENSG00000262660 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1348449824 Functional Loss SNV dbSNP153 33..33 33 - - - 42465 RMVar_ID_42465 Human_SNP_ID_634671083 A-to-I Human chr17 + 81706288 81706288 81706288 CATGTTTTTATTTATTTATGAAACCGAGTCTCACTCTGTCACCCAGGCTGGAGTGCAATGGCGCG CATGTTTTTATTTATTTATGAAACCGAGTCTCGCTCTGTCACCCAGGCTGGAGTGCAATGGCGCG A G MRPL12,AC139530.2 Ensembl:ENSG00000262814,Ensembl:ENSG00000262660 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1047467507 Functional Loss SNV dbSNP153 33..33 33 - - - 42466 RMVar_ID_42466 Human_SNP_ID_634675397 A-to-I Human chr17 + 81718694 81718694 81718694 CTTTTCGGCCAGGCACGGTGGCTCACGCCTGTAATCCCAACACTTTGGGAGGCCAAGGCGGGCAG CTTTTCGGCCAGGCACGGTGGCTCACGCCTGTGATCCCAACACTTTGGGAGGCCAAGGCGGGCAG A G SLC25A10,AC139530.2 Ensembl:ENSG00000183048,Ensembl:ENSG00000262660 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1198017635 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25331203 RMVar_hsa_circ_91527,RMVar_hsa_circ_187753 42467 RMVar_ID_42467 Human_SNP_ID_634675406 A-to-I Human chr17 + 81718716 81718716 81718716 TCACGCCTGTAATCCCAACACTTTGGGAGGCCAAGGCGGGCAGATCACAAGTCAGGAGTTGGAGA TCACGCCTGTAATCCCAACACTTTGGGAGGCCGAGGCGGGCAGATCACAAGTCAGGAGTTGGAGA A G SLC25A10,AC139530.2 Ensembl:ENSG00000183048,Ensembl:ENSG00000262660 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1447822051 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91527,RMVar_hsa_circ_187753 42468 RMVar_ID_42468 Human_SNP_ID_634675432 A-to-I Human chr17 + 81718757 81718757 81718757 AGATCACAAGTCAGGAGTTGGAGACCAGCCTGACCAACATGGTGAAACCCCGTCTCTACTAAAAA AGATCACAAGTCAGGAGTTGGAGACCAGCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAA A G SLC25A10,AC139530.2 Ensembl:ENSG00000183048,Ensembl:ENSG00000262660 Protein coding,Protein coding intron,intron GSE38233;GSE99789 cultured B-cells;esophageal squamous carcinoma cells,EC109 - 24183664,29796672 RNA-Seq:(High) rs1365429946 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91527,RMVar_hsa_circ_187753 42469 RMVar_ID_42469 Human_SNP_ID_634675449 A-to-I Human chr17 + 81718802 81718802 81718802 AACCCCGTCTCTACTAAAAATGCAAAAAAATTAGCTGGGCCTGGTGGCGCACGCCTGTAATCCCA AACCCCGTCTCTACTAAAAATGCAAAAAAATTGGCTGGGCCTGGTGGCGCACGCCTGTAATCCCA A G SLC25A10,AC139530.2 Ensembl:ENSG00000183048,Ensembl:ENSG00000262660 Protein coding,Protein coding intron,intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs572219237 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91527,RMVar_hsa_circ_187753 42470 RMVar_ID_42470 Human_SNP_ID_634675543 A-to-I Human chr17 + 81719071 81719071 81719071 CTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCGCCCGCCACCATGCCCGGCTAATTTTT CTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTGCAGGCGCCCGCCACCATGCCCGGCTAATTTTT A G SLC25A10,AC139530.2 Ensembl:ENSG00000183048,Ensembl:ENSG00000262660 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1237167532 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91527,RMVar_hsa_circ_187753 42471 RMVar_ID_42471 Human_SNP_ID_634675625 A-to-I Human chr17 + 81719341 81719341 81719341 CTGCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGTCACTGTGCCCGGCCAAAAACA CTGCCGCCTCAGCCTCCCAAAGTGCTGGGATTCCAGGTGTGAGTCACTGTGCCCGGCCAAAAACA A C SLC25A10,AC139530.2 Ensembl:ENSG00000183048,Ensembl:ENSG00000262660 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1359863945 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23172235 RMVar_hsa_circ_91527,RMVar_hsa_circ_187753 42472 RMVar_ID_42472 Human_SNP_ID_634692219 A-to-I Human chr17 - 81822816 81822816 81822816 TTTTGTCCTTGAAGTGGTCAGGATACAGGACAAGGGCAGCCCCACCCCATCCAGCCTGGGCTCCC TTTTGTCCTTGAAGTGGTCAGGATACAGGACAGGGGCAGCCCCACCCCATCCAGCCTGGGCTCCC T C MCRIP1 Ensembl:ENSG00000225663 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-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 42473 RMVar_ID_42473 Human_SNP_ID_634693491 A-to-I Human chr17 - 81826399 81826399 81826399 CCCACCCCAGCCTCTGAGTAGCTGGGACTACAAGTGCATGCTGCCACACCAGGTGTGTTCATATG CCCACCCCAGCCTCTGAGTAGCTGGGACTACATGTGCATGCTGCCACACCAGGTGTGTTCATATG T A MCRIP1 Ensembl:ENSG00000225663 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1310037557 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23755083 Human_Splice_Rec_1881895,Human_Splice_Rec_1881923,Human_Splice_Rec_1881977 RMVar_hsa_circ_82677,RMVar_hsa_circ_125951,RMVar_hsa_circ_187758,RMVar_hsa_circ_187759 42474 RMVar_ID_42474 Human_SNP_ID_634693624 A-to-I Human chr17 - 81826732 81826732 81826732 CTCACTGCACCTCCACCTCCCGGGTTCAAGCGATTCTCCTGTTTCAGCCTCCCGAGTAGCTGGGA CTCACTGCACCTCCACCTCCCGGGTTCAAGCGGTTCTCCTGTTTCAGCCTCCCGAGTAGCTGGGA T C MCRIP1 Ensembl:ENSG00000225663 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1455296940 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82677,RMVar_hsa_circ_187759 42475 RMVar_ID_42475 Human_SNP_ID_634693639 A-to-I Human chr17 - 81826761 81826761 81826761 CAGGCTGGAGTGCGTTGGCGCGATCTTGGCTCACTGCACCTCCACCTCCCGGGTTCAAGCGATTC CAGGCTGGAGTGCGTTGGCGCGATCTTGGCTCCCTGCACCTCCACCTCCCGGGTTCAAGCGATTC T G MCRIP1 Ensembl:ENSG00000225663 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1237494928 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82677,RMVar_hsa_circ_187759 42476 RMVar_ID_42476 Human_SNP_ID_634693890 A-to-I Human chr17 - 81827436 81827436 81827436 AAATCCCGTCTCTACTAATAATACAAAAAATTAGCTGGGCGTGGTGGCGGGCTTCTGTAGTCCCA AAATCCCGTCTCTACTAATAATACAAAAAATTTGCTGGGCGTGGTGGCGGGCTTCTGTAGTCCCA T A MCRIP1 Ensembl:ENSG00000225663 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs938474672 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82677,RMVar_hsa_circ_187759 42477 RMVar_ID_42477 Human_SNP_ID_634694114 A-to-I Human chr17 - 81828059 81828059 81828059 CTGTATGGGTGCAGCTGGGTGTGGTAGCTCACACCTGTAATCTCAGCACTTTGGGAGGCCGAAGC CTGTATGGGTGCAGCTGGGTGTGGTAGCTCACGCCTGTAATCTCAGCACTTTGGGAGGCCGAAGC T C MCRIP1 Ensembl:ENSG00000225663 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1365739368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23755088 RMVar_hsa_circ_82677,RMVar_hsa_circ_187759 42478 RMVar_ID_42478 Human_SNP_ID_634694116 A-to-I Human chr17 - 81828066 81828066 81828066 TAAAAAACTGTATGGGTGCAGCTGGGTGTGGTAGCTCACACCTGTAATCTCAGCACTTTGGGAGG TAAAAAACTGTATGGGTGCAGCTGGGTGTGGTGGCTCACACCTGTAATCTCAGCACTTTGGGAGG T C MCRIP1 Ensembl:ENSG00000225663 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1011043469 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6651888 RMVar_hsa_circ_82677,RMVar_hsa_circ_187759 42479 RMVar_ID_42479 Human_SNP_ID_634704997 A-to-I Human chr17 + 81862590 81862590 81862590 GGCGATCTCGGCTCACTCCACCTCCCGGATTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGC GGCGATCTCGGCTCACTCCACCTCCCGGATTCGAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGC A G lnc-ANAPC11-7,lnc-ANAPC11-7:2 RNACentral:URS0000D58631,RNACentral:URS0000D57225 lincRNA,lincRNA exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1044028954 Functional Loss SNV dbSNP153 33..33 33 - - - 42480 RMVar_ID_42480 Human_SNP_ID_634707076 A-to-I Human chr17 - 81868810 81868803 81868810 ACGGACGACGGACAGGCGGATGTGTCCCCCCCAGCCCCTCCCCTCCCCATACCAAAGTGCTGACA ACGGACGACGGACAGGCGGATGTGTCCCCCCC_______CCCCTCCCCATACCAAAGTGCTGACA GAGGGGCT G ARHGDIA Ensembl:ENSG00000141522 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1264577194 Functional Loss DEL dbSNP153 33..39 33 - - - Human_RBP_ID_48537,Human_RBP_ID_502890,Human_RBP_ID_765523,Human_RBP_ID_4480879,Human_RBP_ID_5129798,Human_RBP_ID_6652104,Human_RBP_ID_8823492,Human_RBP_ID_17902972,Human_RBP_ID_18942435,Human_RBP_ID_23755196,Human_RBP_ID_27262442 Human_miRNA_ID_1357696,Human_miRNA_ID_1560221,Human_miRNA_ID_2368129,Human_miRNA_ID_2368130,Human_miRNA_ID_2391089,Human_miRNA_ID_2391090,Human_miRNA_ID_2592334,Human_miRNA_ID_2592335,Human_miRNA_ID_2685951,Human_miRNA_ID_2685952 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 42481 RMVar_ID_42481 Human_SNP_ID_634707081 A-to-I Human chr17 - 81868810 81868808 81868810 ACGGACGACGGACAGGCGGATGTGTCCCCCCCAGCCCCTCCCCTCCCCATACCAAAGTGCTGACA ACGGACGACGGACAGGCGGATGTGTCCCCCCC__CCCCTCCCCTCCCCATACCAAAGTGCTGACA GCT G ARHGDIA Ensembl:ENSG00000141522 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1555604898 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_48537,Human_RBP_ID_502890,Human_RBP_ID_765523,Human_RBP_ID_4480879,Human_RBP_ID_5129798,Human_RBP_ID_6652104,Human_RBP_ID_8823492,Human_RBP_ID_17902972,Human_RBP_ID_18942435,Human_RBP_ID_23755196,Human_RBP_ID_27262442 Human_miRNA_ID_1357696,Human_miRNA_ID_1560221,Human_miRNA_ID_2368129,Human_miRNA_ID_2368130,Human_miRNA_ID_2391089,Human_miRNA_ID_2391090,Human_miRNA_ID_2592334,Human_miRNA_ID_2592335,Human_miRNA_ID_2685951,Human_miRNA_ID_2685952 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 42482 RMVar_ID_42482 Human_SNP_ID_634707086 A-to-I Human chr17 - 81868810 81868810 81868810 ACGGACGACGGACAGGCGGATGTGTCCCCCCCAGCCCCTCCCCTCCCCATACCAAAGTGCTGACA ACGGACGACGGACAGGCGGATGTGTCCCCCCCCGCCCCTCCCCTCCCCATACCAAAGTGCTGACA T G ARHGDIA Ensembl:ENSG00000141522 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs897038186 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_48537,Human_RBP_ID_502890,Human_RBP_ID_765523,Human_RBP_ID_4480879,Human_RBP_ID_5129798,Human_RBP_ID_6652104,Human_RBP_ID_8823492,Human_RBP_ID_17902972,Human_RBP_ID_18942435,Human_RBP_ID_23755196,Human_RBP_ID_27262442 Human_miRNA_ID_1357696,Human_miRNA_ID_1560221,Human_miRNA_ID_2368129,Human_miRNA_ID_2368130,Human_miRNA_ID_2391089,Human_miRNA_ID_2391090,Human_miRNA_ID_2592334,Human_miRNA_ID_2592335,Human_miRNA_ID_2685951,Human_miRNA_ID_2685952 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 42483 RMVar_ID_42483 Human_SNP_ID_634708672 A-to-I Human chr17 + 81872415 81872414 81872416 ATTGATTGATTATTTTTTTGAGACGTAGTCTCAGTGTCGCCCAGGCTTGAGTACAATGGCACAAT ATTGATTGATTATTTTTTTGAGACGTAGTCTC__TGTCGCCCAGGCTTGAGTACAATGGCACAAT CAG C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1274746969 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_2526504,Human_RBP_ID_13200295 42484 RMVar_ID_42484 Human_SNP_ID_634710728 A-to-I Human chr17 - 81879155 81879155 81879155 CTGTTGTTTTTGTGTTTGACCTGTAGCATCTAAGTACTGGTTTCAAAAGTTGCCTAGATGAGTTC CTGTTGTTTTTGTGTTTGACCTGTAGCATCTAGGTACTGGTTTCAAAAGTTGCCTAGATGAGTTC T C AC145207.5 Ensembl:ENSG00000263731 lincRNA exon GSE100210;GSE112787 HepG2 cell line;293 Flip-In T-REx cells,empty vector - 29129909,29967493 RNA-Seq:(High) rs541048429 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_502945,Human_RBP_ID_1092472,Human_RBP_ID_1185110,Human_RBP_ID_1370257,Human_RBP_ID_1545186,Human_RBP_ID_1871018,Human_RBP_ID_3539826,Human_RBP_ID_6652172,Human_RBP_ID_8193568,Human_RBP_ID_8823505,Human_RBP_ID_13200373,Human_RBP_ID_17262404,Human_RBP_ID_17377928,Human_RBP_ID_17494555,Human_RBP_ID_18297061,Human_RBP_ID_20282296,Human_RBP_ID_22807406,Human_RBP_ID_23755222,Human_RBP_ID_27670151 Human_miRNA_ID_3189741,Human_miRNA_ID_3213963 42485 RMVar_ID_42485 Human_SNP_ID_634711058 A-to-I Human chr17 - 81880418 81880418 81880418 TGGAGTCTCACTTTTGCCGAGGCTGTAGTGCAATGGCGCCATCTCAGCTCACTGCAACCTCCGCC TGGAGTCTCACTTTTGCCGAGGCTGTAGTGCAGTGGCGCCATCTCAGCTCACTGCAACCTCCGCC T C AC145207.5 Ensembl:ENSG00000263731 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027512729 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6652245,Human_RBP_ID_13200437 42486 RMVar_ID_42486 Human_SNP_ID_634711168 A-to-I Human chr17 - 81880744 81880744 81880744 ACCTCATGATCCATCCGCCTTGGCCTCCCAAAAGTGCTGGGATTACAGGCCTGAGCCACCACGCC ACCTCATGATCCATCCGCCTTGGCCTCCCAAACGTGCTGGGATTACAGGCCTGAGCCACCACGCC T G AC145207.5 Ensembl:ENSG00000263731 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1247411529 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13200467 42487 RMVar_ID_42487 Human_SNP_ID_634711326 A-to-I Human chr17 - 81881201 81881201 81881201 CCAAAGTGTTGGAATTACAGGCCTGAGCCACCACACCGAACATAGCCTATTAATGTCAGCCTATT CCAAAGTGTTGGAATTACAGGCCTGAGCCACCGCACCGAACATAGCCTATTAATGTCAGCCTATT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1289592986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6652271,Human_RBP_ID_8823532,Human_RBP_ID_13200484,Human_RBP_ID_17494570 42488 RMVar_ID_42488 Human_SNP_ID_634711334 A-to-I Human chr17 - 81881221 81881221 81881221 GATCCTCCTGCCTTGGTCTCCCAAAGTGTTGGAATTACAGGCCTGAGCCACCACACCGAACATAG GATCCTCCTGCCTTGGTCTCCCAAAGTGTTGGGATTACAGGCCTGAGCCACCACACCGAACATAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1047140958 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6652271,Human_RBP_ID_8823532,Human_RBP_ID_13200484,Human_RBP_ID_17494570,Human_RBP_ID_17693352,Human_RBP_ID_23172356 42489 RMVar_ID_42489 Human_SNP_ID_634711349 A-to-I Human chr17 - 81881291 81881291 81881291 TTTTTAAAACTTTGTATAGATGGGGTCTCACTATGTTGCCCAGGTTGGTCTTGAACTCTTGTGCT TTTTTAAAACTTTGTATAGATGGGGTCTCACTGTGTTGCCCAGGTTGGTCTTGAACTCTTGTGCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs943029551 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4459907,Human_RBP_ID_13200492 42490 RMVar_ID_42490 Human_SNP_ID_634711369 A-to-I Human chr17 - 81881351 81881351 81881351 CTCCCACCTCAGCCTCCTTAGTAGCTGGGACTACAGACACCCACCACCGCGCCTGGCTGATTTTT CTCCCACCTCAGCCTCCTTAGTAGCTGGGACTGCAGACACCCACCACCGCGCCTGGCTGATTTTT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1168873268 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13200497 42491 RMVar_ID_42491 Human_SNP_ID_634711400 A-to-I Human chr17 - 81881441 81881441 81881441 TTGAGACAAGGTCTCCCTCTGATGTCCAGGCTAGAGTGCAGTGGCGCAAACACAGCTCACTGCAT TTGAGACAAGGTCTCCCTCTGATGTCCAGGCTGGAGTGCAGTGGCGCAAACACAGCTCACTGCAT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs778558117 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6652298,Human_RBP_ID_23172361,Human_RBP_ID_26461142 42492 RMVar_ID_42492 Human_SNP_ID_634711406 A-to-I Human chr17 - 81881452 81881452 81881452 AAAATTGTGTTTTGAGACAAGGTCTCCCTCTGATGTCCAGGCTAGAGTGCAGTGGCGCAAACACA AAAATTGTGTTTTGAGACAAGGTCTCCCTCTGTTGTCCAGGCTAGAGTGCAGTGGCGCAAACACA T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs746849759 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1871026,Human_RBP_ID_6652298,Human_RBP_ID_13200501,Human_RBP_ID_18297084,Human_RBP_ID_23172361 42493 RMVar_ID_42493 Human_SNP_ID_634711553 A-to-I Human chr17 - 81881853 81881853 81881853 TTTTGTAGAAAAACTTGTCTCAGGCTGGGCGCAGTGGCTCACGCCTGTAATCCCGGCACATTGAG TTTTGTAGAAAAACTTGTCTCAGGCTGGGCGCGGTGGCTCACGCCTGTAATCCCGGCACATTGAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs932705705 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13200514,Human_RBP_ID_22807411 42494 RMVar_ID_42494 Human_SNP_ID_634711655 A-to-I Human chr17 - 81882178 81882178 81882178 GACCTTGTGATCCGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCGCC GACCTTGTGATCCGCCCACCTCGGCCTCCCAACGTGCTGGGATTACAGGTGTGAGCCACCGCGCC T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs927882228 Functional Loss SNV dbSNP153 33..33 33 - - - 42495 RMVar_ID_42495 Human_SNP_ID_634711762 A-to-I Human chr17 - 81882368 81882368 81882368 GGCTGGAGTGCAGTGGTGCAATCTCAGCTCACAACAGCCTCTGCCTCCCGGGTCCCCGTTCAAGC GGCTGGAGTGCAGTGGTGCAATCTCAGCTCACTACAGCCTCTGCCTCCCGGGTCCCCGTTCAAGC T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474125942 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6652317,Human_RBP_ID_13200534 42496 RMVar_ID_42496 Human_SNP_ID_634711763 A-to-I Human chr17 - 81882368 81882368 81882368 GGCTGGAGTGCAGTGGTGCAATCTCAGCTCACAACAGCCTCTGCCTCCCGGGTCCCCGTTCAAGC GGCTGGAGTGCAGTGGTGCAATCTCAGCTCACGACAGCCTCTGCCTCCCGGGTCCCCGTTCAAGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474125942 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6652317,Human_RBP_ID_13200534 42497 RMVar_ID_42497 Human_SNP_ID_634711765 A-to-I Human chr17 - 81882375 81882375 81882375 TAGCCCAGGCTGGAGTGCAGTGGTGCAATCTCAGCTCACAACAGCCTCTGCCTCCCGGGTCCCCG TAGCCCAGGCTGGAGTGCAGTGGTGCAATCTCGGCTCACAACAGCCTCTGCCTCCCGGGTCCCCG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1483419118 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13200534,Human_RBP_ID_23172379,Human_RBP_ID_25331465 42498 RMVar_ID_42498 Human_SNP_ID_634712018 A-to-I Human chr17 - 81883000 81883000 81883000 TATTTTTAGTAGAGATGGGGTTCCACCTTGTTAGCCAGGATGGTCTCTATCTCCTGACCTCGTGA TATTTTTAGTAGAGATGGGGTTCCACCTTGTTCGCCAGGATGGTCTCTATCTCCTGACCTCGTGA T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335771580 Functional Loss SNV dbSNP153 33..33 33 - - - 42499 RMVar_ID_42499 Human_SNP_ID_634712357 A-to-I Human chr17 - 81883796 81883796 81883796 CTCTGTCACACAGGCTGGAGTGCAGTGGCGCAATCTCCACTCACTGCAAGCTCCGCCTCCCAGGT CTCTGTCACACAGGCTGGAGTGCAGTGGCGCAGTCTCCACTCACTGCAAGCTCCGCCTCCCAGGT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1020522975 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13200591,Human_RBP_ID_23172398 42500 RMVar_ID_42500 Human_SNP_ID_634712466 A-to-I Human chr17 - 81884069 81884066 81884070 TCACCTCACTGCAACCTCCGCCTCCCGGGTTGAATCGATTCTCCTGCCTCAGCCTCCTGAGTAGC TCACCTCACTGCAACCTCCGCCTCCCGGGTT____CGATTCTCCTGCCTCAGCCTCCTGAGTAGC GATTC G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1440637627 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_13200596,Human_RBP_ID_17693356 42501 RMVar_ID_42501 Human_SNP_ID_634713208 A-to-I Human chr17 - 81886626 81886626 81886626 AGCACTTTGAGAATGAGATGGGAAGGGGGACAAGGGAGCTCCAGAGTTCTGCCTGACCCCACTGT AGCACTTTGAGAATGAGATGGGAAGGGGGACAGGGGAGCTCCAGAGTTCTGCCTGACCCCACTGT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1436296446 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1011152,Human_RBP_ID_1185132,Human_RBP_ID_6652506,Human_RBP_ID_13200734,Human_RBP_ID_17903095,Human_RBP_ID_18439883,Human_RBP_ID_23129882 42502 RMVar_ID_42502 Human_SNP_ID_634713278 A-to-I Human chr17 - 81886827 81886827 81886827 AAAACCCTATCTCTACTAAAAATACAAAAGTTAGCTGAGTGTGGTGGCGTGCTCCTGTGGTCTCA AAAACCCTATCTCTACTAAAAATACAAAAGTTGGCTGAGTGTGGTGGCGTGCTCCTGTGGTCTCA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965549704 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6652512,Human_RBP_ID_23755262 42503 RMVar_ID_42503 Human_SNP_ID_634713284 A-to-I Human chr17 - 81886839 81886839 81886839 AGGCAACATGGCAAAACCCTATCTCTACTAAAAATACAAAAGTTAGCTGAGTGTGGTGGCGTGCT AGGCAACATGGCAAAACCCTATCTCTACTAAAGATACAAAAGTTAGCTGAGTGTGGTGGCGTGCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs932935605 Functional Loss SNV dbSNP153 33..33 33 - - - 42504 RMVar_ID_42504 Human_SNP_ID_634713285 A-to-I Human chr17 - 81886842 81886842 81886842 CCTAGGCAACATGGCAAAACCCTATCTCTACTAAAAATACAAAAGTTAGCTGAGTGTGGTGGCGT CCTAGGCAACATGGCAAAACCCTATCTCTACTGAAAATACAAAAGTTAGCTGAGTGTGGTGGCGT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1397339629 Functional Loss SNV dbSNP153 33..33 33 - - - 42505 RMVar_ID_42505 Human_SNP_ID_634713327 A-to-I Human chr17 - 81886984 81886983 81886985 GATTGTGCCATTGCACTCCAGTCTGGACAACAAGAGTGAACTCCGTCTCAAAAAGGAGTAGGGCA GATTGTGCCATTGCACTCCAGTCTGGACAAC__GAGTGAACTCCGTCTCAAAAAGGAGTAGGGCA CTT C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1365564718 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_1545215,Human_RBP_ID_6652517,Human_RBP_ID_8466420,Human_RBP_ID_13200749,Human_RBP_ID_23172424,Human_RBP_ID_27156959 42506 RMVar_ID_42506 Human_SNP_ID_634713405 A-to-I Human chr17 - 81887222 81887222 81887222 TGGGGCGGCTGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGGGGCAGGCAG TGGGGCGGCTGGGCGCGGTGGCTCACGCCTGTGATCCCAGCACTTTGGGAGGCTGGGGCAGGCAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893583008 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6652520 42507 RMVar_ID_42507 Human_SNP_ID_634715658 A-to-I Human chr17 + 81892943 81892943 81892943 GCAGTGGTGTGATCTTGGCTCACTGCAGCCTCAAACTCCTGGGCTCGAGCTATCCTCCCACGTCA GCAGTGGTGTGATCTTGGCTCACTGCAGCCTCCAACTCCTGGGCTCGAGCTATCCTCCCACGTCA A C ANAPC11 Ensembl:ENSG00000141552 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs889615882 Functional Loss SNV dbSNP153 33..33 33 - - - 42508 RMVar_ID_42508 Human_SNP_ID_634716672 A-to-I Human chr17 + 81895821 81895821 81895821 GAAACGCCATCTCTACTAAAAATACAAAAATTAGCTGGGTGTGTGGCGTGTGCCTGTAATCCCAG GAAACGCCATCTCTACTAAAAATACAAAAATTTGCTGGGTGTGTGGCGTGTGCCTGTAATCCCAG A T ANAPC11 Ensembl:ENSG00000141552 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs950439776 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22587193 42509 RMVar_ID_42509 Human_SNP_ID_634725497 A-to-I Human chr17 - 81921510 81921510 81921510 CCAGAAGGCCGTCCTCTTTGATATCTTTTGCAATTGTACCGAAAGTGACTTACTCCTCTGCCCTT CCAGAAGGCCGTCCTCTTTGATATCTTTTGCAGTTGTACCGAAAGTGACTTACTCCTCTGCCCTT T C MAFG Ensembl:ENSG00000197063 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1195853711 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_132257,Human_RBP_ID_1545293,Human_RBP_ID_1871092,Human_RBP_ID_2526560,Human_RBP_ID_3539883,Human_RBP_ID_13201310,Human_RBP_ID_18712012,Human_RBP_ID_23755369 Human_miRNA_ID_685077,Human_miRNA_ID_887622,Human_miRNA_ID_1064274,Human_miRNA_ID_1075581,Human_miRNA_ID_2249552 RMVar_hsa_circ_106600,RMVar_hsa_circ_116913,RMVar_hsa_circ_187796,RMVar_hsa_circ_187797 42510 RMVar_ID_42510 Human_SNP_ID_634725498 A-to-I Human chr17 - 81921510 81921510 81921510 CCAGAAGGCCGTCCTCTTTGATATCTTTTGCAATTGTACCGAAAGTGACTTACTCCTCTGCCCTT CCAGAAGGCCGTCCTCTTTGATATCTTTTGCACTTGTACCGAAAGTGACTTACTCCTCTGCCCTT T G MAFG Ensembl:ENSG00000197063 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1195853711 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_132257,Human_RBP_ID_1545293,Human_RBP_ID_1871092,Human_RBP_ID_2526560,Human_RBP_ID_3539883,Human_RBP_ID_13201310,Human_RBP_ID_18712012,Human_RBP_ID_23755369 Human_miRNA_ID_685077,Human_miRNA_ID_887622,Human_miRNA_ID_1064274,Human_miRNA_ID_1075581,Human_miRNA_ID_2249552 RMVar_hsa_circ_106600,RMVar_hsa_circ_116913,RMVar_hsa_circ_187796,RMVar_hsa_circ_187797 42511 RMVar_ID_42511 Human_SNP_ID_634729477 A-to-I Human chr17 - 81933282 81933282 81933282 TGGACAAGGTGAAGCTGGACTCCCCTGCAGGGACCGCTCTGTCACCTTCTGGCCACACCAAGCTG TGGACAAGGTGAAGCTGGACTCCCCTGCAGGGTCCGCTCTGTCACCTTCTGGCCACACCAAGCTG T A PYCR1 Ensembl:ENSG00000183010 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs752293774 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_236995,Human_RBP_ID_18989610 Human_Splice_Rec_1882886,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 Human_miRNA_ID_2878077 RMVar_hsa_circ_87352,RMVar_hsa_circ_112525,RMVar_hsa_circ_187799,RMVar_hsa_circ_83403,RMVar_hsa_circ_187800,RMVar_hsa_circ_187798 42512 RMVar_ID_42512 Human_SNP_ID_634746525 A-to-I Human chr17 + 81984094 81984094 81984094 CTGCTGGTCTGGAACTGCTGACCTCATGATCTACCCGCCTCGGCCTCCCAAAGTCCTCCCAAAGG CTGCTGGTCTGGAACTGCTGACCTCATGATCTCCCCGCCTCGGCCTCCCAAAGTCCTCCCAAAGG A C ASPSCR1 Ensembl:ENSG00000169696 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs527654671 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119350,RMVar_hsa_circ_288739,RMVar_hsa_circ_56317,RMVar_hsa_circ_187807,RMVar_hsa_circ_27983,RMVar_hsa_circ_187806,RMVar_hsa_circ_299416,RMVar_hsa_circ_8085,RMVar_hsa_circ_187809 42513 RMVar_ID_42513 Human_SNP_ID_634746592 A-to-I Human chr17 + 81984336 81984336 81984336 GCCGCAAGGGCAGCCTGTAATCCCAGCACTTTAGGAGGCCGAGGCGGGCAGATCACCTGAGGTCA GCCGCAAGGGCAGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCAGATCACCTGAGGTCA A G ASPSCR1 Ensembl:ENSG00000169696 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1567955852 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119350,RMVar_hsa_circ_288739,RMVar_hsa_circ_56317,RMVar_hsa_circ_187807,RMVar_hsa_circ_27983,RMVar_hsa_circ_187806,RMVar_hsa_circ_299416,RMVar_hsa_circ_8085,RMVar_hsa_circ_187809 42514 RMVar_ID_42514 Human_SNP_ID_634752875 A-to-I Human chr17 + 82002909 82002909 82002909 TAACTTTTTTTTTTTCGAGACAGGGTCTGTCTATGTTGCCTAGCCTGGAGTGTGGTGGTGCGATC TAACTTTTTTTTTTTCGAGACAGGGTCTGTCTGTGTTGCCTAGCCTGGAGTGTGGTGGTGCGATC A G ASPSCR1 Ensembl:ENSG00000169696 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1276379948 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56317,RMVar_hsa_circ_27983,RMVar_hsa_circ_55539 42515 RMVar_ID_42515 Human_SNP_ID_634752876 A-to-I Human chr17 + 82002909 82002909 82002909 TAACTTTTTTTTTTTCGAGACAGGGTCTGTCTATGTTGCCTAGCCTGGAGTGTGGTGGTGCGATC TAACTTTTTTTTTTTCGAGACAGGGTCTGTCTTTGTTGCCTAGCCTGGAGTGTGGTGGTGCGATC A T ASPSCR1 Ensembl:ENSG00000169696 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1276379948 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56317,RMVar_hsa_circ_27983,RMVar_hsa_circ_55539 42516 RMVar_ID_42516 Human_SNP_ID_634752948 A-to-I Human chr17 + 82003174 82003174 82003174 CCAGCCTAAAATAACTTTTCTTGGCTGGGTACAGTGGCTCGCACCTATAATCACAGCACTTCGGG CCAGCCTAAAATAACTTTTCTTGGCTGGGTACGGTGGCTCGCACCTATAATCACAGCACTTCGGG A G ASPSCR1 Ensembl:ENSG00000169696 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1454327428 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17566279 RMVar_hsa_circ_56317,RMVar_hsa_circ_27983,RMVar_hsa_circ_55539 42517 RMVar_ID_42517 Human_SNP_ID_634755463 A-to-I Human chr17 + 82010382 82010382 82010382 AAACCCCATCTCTACTAAAAATACAAAAAATTAGTCAGGAGAGGTGGCGCACGCCTGTAGTCCCA AAACCCCATCTCTACTAAAAATACAAAAAATTGGTCAGGAGAGGTGGCGCACGCCTGTAGTCCCA A G ASPSCR1 Ensembl:ENSG00000169696 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs543940770 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27983,RMVar_hsa_circ_46174,RMVar_hsa_circ_55539 42518 RMVar_ID_42518 Human_SNP_ID_634794115 A-to-I Human chr17 - 82111461 82111461 82111461 GGCAGGAGTATCGTTTGAGCCCGGGAGGTTGAAGCTGCAGTGAGCCACGATCACGCCACTGCGCT GGCAGGAGTATCGTTTGAGCCCGGGAGGTTGAGGCTGCAGTGAGCCACGATCACGCCACTGCGCT T C CCDC57 Ensembl:ENSG00000176155 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1478759990 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13202117 RMVar_hsa_circ_187899,RMVar_hsa_circ_85460 42519 RMVar_ID_42519 Human_SNP_ID_634794279 A-to-I Human chr17 - 82112105 82112105 82112105 GTCAGGTGTGGTGGTGCATGCCTGTAATCCCAACTACTCAGGAGGCTGAGGCATGAGAATCACTT GTCAGGTGTGGTGGTGCATGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCATGAGAATCACTT T C CCDC57 Ensembl:ENSG00000176155 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1290198270 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_187899,RMVar_hsa_circ_85460 42520 RMVar_ID_42520 Human_SNP_ID_634794727 A-to-I Human chr17 - 82113863 82113863 82113863 TGGTTCACTGTGGCCTCAACTTTCCAGGCTCAAGTGATCCTCCTGCCTTTGTCTCCTGAGTAGCT TGGTTCACTGTGGCCTCAACTTTCCAGGCTCAGGTGATCCTCCTGCCTTTGTCTCCTGAGTAGCT T C CCDC57 Ensembl:ENSG00000176155 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1405157047 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_187899,RMVar_hsa_circ_85460 42521 RMVar_ID_42521 Human_SNP_ID_634795168 A-to-I Human chr17 - 82115549 82115549 82115549 CCAATATGGTCTTGAACTCCTGGGTTCAAGCAATGCTCCCATGTCAGCCTCCCTAAGCGCTGGGA CCAATATGGTCTTGAACTCCTGGGTTCAAGCAGTGCTCCCATGTCAGCCTCCCTAAGCGCTGGGA T C CCDC57 Ensembl:ENSG00000176155 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs532821903 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23172477 RMVar_hsa_circ_187899,RMVar_hsa_circ_85460 42522 RMVar_ID_42522 Human_SNP_ID_634795288 A-to-I Human chr17 - 82115926 82115926 82115926 TGGCACGGTTGCAGGCACCTGTAAACCCAGCTACTCCAGAGGCTGAGGCAGGAGAATCGCTTGAA TGGCACGGTTGCAGGCACCTGTAAACCCAGCTGCTCCAGAGGCTGAGGCAGGAGAATCGCTTGAA T C CCDC57 Ensembl:ENSG00000176155 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1332113231 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_131917 RMVar_hsa_circ_187899,RMVar_hsa_circ_85460 42523 RMVar_ID_42523 Human_SNP_ID_634797930 A-to-I Human chr17 - 82126098 82126098 82126098 TTTTGTATTTTTAGTAGAGACGGGGTTTCACAATGCTGGGCTGGCTCGTCTCGAACTCCTGACCT TTTTGTATTTTTAGTAGAGACGGGGTTTCACAGTGCTGGGCTGGCTCGTCTCGAACTCCTGACCT T C CCDC57 Ensembl:ENSG00000176155 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1480187354 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13202455,Human_RBP_ID_25331935 RMVar_hsa_circ_187899,RMVar_hsa_circ_85460 42524 RMVar_ID_42524 Human_SNP_ID_634802464 A-to-I Human chr17 - 82142453 82142453 82142453 TAAAAATTAGCCGGGCTTGGTGTTGCGCGCCTATAGTCCCAGCTACTCGGGAGGCTGAGGCAGAA TAAAAATTAGCCGGGCTTGGTGTTGCGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGAA T C CCDC57 Ensembl:ENSG00000176155 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs554554888 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_31577,RMVar_hsa_circ_187899,RMVar_hsa_circ_85460,RMVar_hsa_circ_36569,RMVar_hsa_circ_25796,RMVar_hsa_circ_269498 42525 RMVar_ID_42525 Human_SNP_ID_634817177 A-to-I Human chr17 - 82193384 82193384 82193384 CACAACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTCTCACCATGTTGGCCAGGC CACAACCATGCCTGGCTAATTTTTGTATTTTTGGTAGAGACAGGGTCTCACCATGTTGGCCAGGC T C CCDC57 Ensembl:ENSG00000176155 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs900711865 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6789,RMVar_hsa_circ_31577,RMVar_hsa_circ_25796,RMVar_hsa_circ_333191,RMVar_hsa_circ_356803,RMVar_hsa_circ_187905,RMVar_hsa_circ_369524,RMVar_hsa_circ_12311,RMVar_hsa_circ_187911,RMVar_hsa_circ_88070,RMVar_hsa_circ_266833,RMVar_hsa_circ_376749,RMVar_hsa_circ_98531,RMVar_hsa_circ_187912,RMVar_hsa_circ_284434,RMVar_hsa_circ_336581,RMVar_hsa_circ_359065,RMVar_hsa_circ_335065,RMVar_hsa_circ_24071,RMVar_hsa_circ_187915,RMVar_hsa_circ_187916,RMVar_hsa_circ_187914,RMVar_hsa_circ_25753 42526 RMVar_ID_42526 Human_SNP_ID_634830841 A-to-I Human chr17 + 82237232 82237232 82237232 CGGCGCCCCATGGCCAACGGGCTGGCGGCAGCAGGTAGCCCTGTCTTCCTGTGTGCCCTGAGCCC CGGCGCCCCATGGCCAACGGGCTGGCGGCAGCGGGTAGCCCTGTCTTCCTGTGTGCCCTGAGCCC A G SLC16A3 Ensembl:ENSG00000141526 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs778195547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22444134 Human_Splice_Rec_1884784,Human_Splice_Rec_1884790,Human_Splice_Rec_1884798,Human_Splice_Rec_1884806,Human_Splice_Rec_1884814,Human_Splice_Rec_1884818,Human_Splice_Rec_1884824,Human_Splice_Rec_1884838,Human_Splice_Rec_1884844,Human_Splice_Rec_1884850,Human_Splice_Rec_1884858,Human_Splice_Rec_1884864,Human_Splice_Rec_1884872,Human_Splice_Rec_1884878,Human_Splice_Rec_1884884,Human_Splice_Rec_1884888 Human_miRNA_ID_2513087,Human_miRNA_ID_3055907,Human_miRNA_ID_3058149 RMVar_hsa_circ_13571,RMVar_hsa_circ_187919,RMVar_hsa_circ_312414 42527 RMVar_ID_42527 Human_SNP_ID_634838226 A-to-I Human chr17 + 82256278 82256278 82256278 CATGCCTGTAATCCTAGCACTTTGGGAGGCTGAAACGGGAGGACTGCTTGAGCTCAGAAGTTCGA CATGCCTGTAATCCTAGCACTTTGGGAGGCTGCAACGGGAGGACTGCTTGAGCTCAGAAGTTCGA A C SLC16A3 Ensembl:ENSG00000141526 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs989647243 Functional Loss SNV dbSNP153 33..33 33 - - - 42528 RMVar_ID_42528 Human_SNP_ID_634838244 A-to-I Human chr17 - 82256340 82256340 82256340 CCCACCTAATTTCCAGAATTTTTTGTAGAGACAAGGGTCTCCCTTTGTTATCCAGGCTGGTCTCG CCCACCTAATTTCCAGAATTTTTTGTAGAGACTAGGGTCTCCCTTTGTTATCCAGGCTGGTCTCG T A CSNK1D Ensembl:ENSG00000141551 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1269932467 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2526876,Human_RBP_ID_13204076 RMVar_hsa_circ_293756,RMVar_hsa_circ_187926,RMVar_hsa_circ_343316,RMVar_hsa_circ_339301,RMVar_hsa_circ_368813 42529 RMVar_ID_42529 Human_SNP_ID_634842137 A-to-I Human chr17 - 82268859 82268859 82268859 GAATGCCTGACCTCAAGCGATCCATCAGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAA GAATGCCTGACCTCAAGCGATCCATCAGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAA T C CSNK1D Ensembl:ENSG00000141551 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1272512373 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13204680 RMVar_hsa_circ_29402 42530 RMVar_ID_42530 Human_SNP_ID_634842150 A-to-I Human chr17 - 82268914 82268914 82268914 TTTTTTTGTATTTATAGTAGGGACGGGGTTTCACCATGTGGGCCAGGCTGGTCTCGAATGCCTGA TTTTTTTGTATTTATAGTAGGGACGGGGTTTCCCCATGTGGGCCAGGCTGGTCTCGAATGCCTGA T G CSNK1D Ensembl:ENSG00000141551 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1020733706 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29402 42531 RMVar_ID_42531 Human_SNP_ID_634842171 A-to-I Human chr17 - 82268975 82268975 82268975 CTTCCGCATCAACCTCCTGAGTAGCTGGGGTTAGAGGCGCACACCAGCATGCCTGGCTAATTTTT CTTCCGCATCAACCTCCTGAGTAGCTGGGGTTCGAGGCGCACACCAGCATGCCTGGCTAATTTTT T G CSNK1D Ensembl:ENSG00000141551 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs938257252 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6653339 RMVar_hsa_circ_29402 42532 RMVar_ID_42532 Human_SNP_ID_634842181 A-to-I Human chr17 - 82269011 82269011 82269011 CTCACTGCAACCCCTGCCTTCTGGGTTCAAGCAGTTCTTCCGCATCAACCTCCTGAGTAGCTGGG CTCACTGCAACCCCTGCCTTCTGGGTTCAAGCGGTTCTTCCGCATCAACCTCCTGAGTAGCTGGG T C CSNK1D Ensembl:ENSG00000141551 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs375719959 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29402 42533 RMVar_ID_42533 Human_SNP_ID_634842187 A-to-I Human chr17 - 82269045 82269045 82269045 TTGCCTAGGCTGGGGTGCAGTGGCGCGATCTCAGCTCACTGCAACCCCTGCCTTCTGGGTTCAAG TTGCCTAGGCTGGGGTGCAGTGGCGCGATCTCGGCTCACTGCAACCCCTGCCTTCTGGGTTCAAG T C CSNK1D Ensembl:ENSG00000141551 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs922672088 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13243527,Human_RBP_ID_26976164 RMVar_hsa_circ_29402 42534 RMVar_ID_42534 Human_SNP_ID_634842188 A-to-I Human chr17 - 82269045 82269045 82269045 TTGCCTAGGCTGGGGTGCAGTGGCGCGATCTCAGCTCACTGCAACCCCTGCCTTCTGGGTTCAAG TTGCCTAGGCTGGGGTGCAGTGGCGCGATCTCCGCTCACTGCAACCCCTGCCTTCTGGGTTCAAG T G CSNK1D Ensembl:ENSG00000141551 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs922672088 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13243527,Human_RBP_ID_26976164 RMVar_hsa_circ_29402 42535 RMVar_ID_42535 Human_SNP_ID_634842205 A-to-I Human chr17 - 82269090 82269088 82269091 TGCTTTTTTTTTTTTTTTTTTTTTTTAAGACAAAGTATCATTCTGTTGCCTAGGCTGGGGTGCAG TGCTTTTTTTTTTTTTTTTTTTTTTTAAGAC___GTATCATTCTGTTGCCTAGGCTGGGGTGCAG CTTT C CSNK1D Ensembl:ENSG00000141551 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1313410546 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_13204685 RMVar_hsa_circ_29402 42536 RMVar_ID_42536 Human_SNP_ID_634844706 A-to-I Human chr17 + 82276885 82276885 82276885 TTGAACTTCTGACCTCGTGATCCGCCCGCCTTAGCCTCCCAAAGTGCTGAGATTATAGGCATGAG TTGAACTTCTGACCTCGTGATCCGCCCGCCTTGGCCTCCCAAAGTGCTGAGATTATAGGCATGAG A G AC132872.5 Ensembl:ENSG00000287737 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs543456901 Functional Loss SNV dbSNP153 33..33 33 - - - 42537 RMVar_ID_42537 Human_SNP_ID_634849923 A-to-I Human chr17 + 82294440 82294440 82294440 ATGGCTCACTGTAACCTCAAATTCTTGGCCTCAAGCGATCCTCCTGCCTCACCCTCCTGAAAGGA ATGGCTCACTGTAACCTCAAATTCTTGGCCTCGAGCGATCCTCCTGCCTCACCCTCCTGAAAGGA A G AC132872.1 Ensembl:ENSG00000260563 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1056869554 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2527021,Human_RBP_ID_5188493 42538 RMVar_ID_42538 Human_SNP_ID_634876467 A-to-I Human chr17 - 82382083 82382083 82382083 CAGCTCACTGCAATCTCTGCCTCCCGGGTTCAAGTGATTCTCCTGCCTCAGACTCCTGAGTAGCT CAGCTCACTGCAATCTCTGCCTCCCGGGTTCACGTGATTCTCCTGCCTCAGACTCCTGAGTAGCT T G AC132938.2 Ensembl:ENSG00000260011 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1449880580 Functional Loss SNV dbSNP153 33..33 33 - - - 42539 RMVar_ID_42539 Human_SNP_ID_634879002 A-to-I Human chr17 - 82389618 82389612 82389618 TGTGCTCCTGTGGTCCCAGCTACTCGGAGCTGAGGCAGGACGACTGCTTGAGCCCAGGAGGTCGA TGTGCTCCTGTGGTCCCAGCTACTCGGAGCTG______GACGACTGCTTGAGCCCAGGAGGTCGA CCTGCCT C OGFOD3 Ensembl:ENSG00000181396 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1031096944 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_503594 42540 RMVar_ID_42540 Human_SNP_ID_634879016 A-to-I Human chr17 - 82389652 82389652 82389652 AGAAACTTTTAAAAAATGTAGCTGGGCGTGGCAGTGTGCTCCTGTGGTCCCAGCTACTCGGAGCT AGAAACTTTTAAAAAATGTAGCTGGGCGTGGCGGTGTGCTCCTGTGGTCCCAGCTACTCGGAGCT T C OGFOD3 Ensembl:ENSG00000181396 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs969353912 Functional Loss SNV dbSNP153 33..33 33 - - - 42541 RMVar_ID_42541 Human_SNP_ID_634886086 A-to-I Human chr17 - 82413687 82413687 82413687 TTTGTAATTTTAGTAGAGACGGTGTTTTGCCTATGTTGCCCAGGCTGATCTCAAACTGCTGACCT TTTGTAATTTTAGTAGAGACGGTGTTTTGCCTGTGTTGCCCAGGCTGATCTCAAACTGCTGACCT T C OGFOD3 Ensembl:ENSG00000181396 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1419545009 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24366,RMVar_hsa_circ_118624,RMVar_hsa_circ_187939 42542 RMVar_ID_42542 Human_SNP_ID_634887120 A-to-I Human chr17 - 82417397 82417397 82417397 CCAGGCTGGTCTCGAACTCTCAACCTCAAGCAATCCGCCCGCCTCAGCCTCCCAAAGTGCTGGGA CCAGGCTGGTCTCGAACTCTCAACCTCAAGCAGTCCGCCCGCCTCAGCCTCCCAAAGTGCTGGGA T C OGFOD3 Ensembl:ENSG00000181396 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs887917844 Functional Loss SNV dbSNP153 33..33 33 - - - 42543 RMVar_ID_42543 Human_SNP_ID_634887121 A-to-I Human chr17 - 82417397 82417397 82417397 CCAGGCTGGTCTCGAACTCTCAACCTCAAGCAATCCGCCCGCCTCAGCCTCCCAAAGTGCTGGGA CCAGGCTGGTCTCGAACTCTCAACCTCAAGCACTCCGCCCGCCTCAGCCTCCCAAAGTGCTGGGA T G OGFOD3 Ensembl:ENSG00000181396 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs887917844 Functional Loss SNV dbSNP153 33..33 33 - - - 42544 RMVar_ID_42544 Human_SNP_ID_634891061 A-to-I Human chr17 - 82431578 82431578 82431578 AAAACCCCGTCTCTACTAAGAAGACAAAAATTAGCTGGGTGTGGTGGCGGGCGCTGTAATCCCAG AAAACCCCGTCTCTACTAAGAAGACAAAAATTGGCTGGGTGTGGTGGCGGGCGCTGTAATCCCAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1038492375 Functional Loss SNV dbSNP153 33..33 33 - - - 42545 RMVar_ID_42545 Human_SNP_ID_634902721 A-to-I Human chr17 + 82467227 82467227 82467227 CACCACCATGTCTGGCTAGCTTTTGTATTTTTAGTAGAGATGGGGTTTCTCCCTTTTGGCCAGGC CACCACCATGTCTGGCTAGCTTTTGTATTTTTCGTAGAGATGGGGTTTCTCCCTTTTGGCCAGGC A C NARF Ensembl:ENSG00000141562 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1390507829 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25332501 RMVar_hsa_circ_187951,RMVar_hsa_circ_274039,RMVar_hsa_circ_293176,RMVar_hsa_circ_348079,RMVar_hsa_circ_187952,RMVar_hsa_circ_303928,RMVar_hsa_circ_330565,RMVar_hsa_circ_187953 42546 RMVar_ID_42546 Human_SNP_ID_634902865 A-to-I Human chr17 + 82467704 82467704 82467704 TTTTTGTATTTTTAGTAGAGATGGGTTTCGCCATGTTGGCCAGGCTGATCTTGAACTCCTGACCT TTTTTGTATTTTTAGTAGAGATGGGTTTCGCCCTGTTGGCCAGGCTGATCTTGAACTCCTGACCT A C NARF Ensembl:ENSG00000141562 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1190960220 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_187951,RMVar_hsa_circ_274039,RMVar_hsa_circ_293176,RMVar_hsa_circ_348079,RMVar_hsa_circ_187952,RMVar_hsa_circ_303928,RMVar_hsa_circ_330565,RMVar_hsa_circ_187953 42547 RMVar_ID_42547 Human_SNP_ID_634902985 A-to-I Human chr17 + 82468188 82468188 82468188 AAAAAATTAGCTGGGTGTAGTGGCAGGTCCCTATAATCCCAGCTACTTGGGAGGCTGAGGCAGGA AAAAAATTAGCTGGGTGTAGTGGCAGGTCCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGA A G NARF Ensembl:ENSG00000141562 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs993124470 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_187951,RMVar_hsa_circ_274039,RMVar_hsa_circ_293176,RMVar_hsa_circ_348079,RMVar_hsa_circ_187952,RMVar_hsa_circ_303928,RMVar_hsa_circ_330565,RMVar_hsa_circ_187953 42548 RMVar_ID_42548 Human_SNP_ID_634904695 A-to-I Human chr17 + 82473488 82473488 82473488 ATCCTGCCTCACCCTCCCGAGTAGCTGGGACTACAGGCGCCTGCCACCACACCCGGCTAATTTCT ATCCTGCCTCACCCTCCCGAGTAGCTGGGACTTCAGGCGCCTGCCACCACACCCGGCTAATTTCT A T NARF Ensembl:ENSG00000141562 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1164437513 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49518,RMVar_hsa_circ_348079,RMVar_hsa_circ_330565,RMVar_hsa_circ_187956,RMVar_hsa_circ_308003,RMVar_hsa_circ_279444 42549 RMVar_ID_42549 Human_SNP_ID_634904857 A-to-I Human chr17 + 82474105 82474105 82474105 TACTACGAATCCTAGCCTGAGGTGTTTGAGCCAAGGAGTTAGAGGCTGCAGTGAGCTATGACTCC TACTACGAATCCTAGCCTGAGGTGTTTGAGCCCAGGAGTTAGAGGCTGCAGTGAGCTATGACTCC A C NARF Ensembl:ENSG00000141562 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1195469415 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49518,RMVar_hsa_circ_348079,RMVar_hsa_circ_330565,RMVar_hsa_circ_187956,RMVar_hsa_circ_308003,RMVar_hsa_circ_279444 42550 RMVar_ID_42550 Human_SNP_ID_634905793 A-to-I Human chr17 + 82477556 82477556 82477556 AAAAAACAACACAGAGTCTTGCTCTGTCATCCAAGCTTGGAGAGCAGTGATGCAATCATAGCTGA AAAAAACAACACAGAGTCTTGCTCTGTCATCCGAGCTTGGAGAGCAGTGATGCAATCATAGCTGA A G NARF Ensembl:ENSG00000141562 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1003449777 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49518,RMVar_hsa_circ_348079,RMVar_hsa_circ_330565,RMVar_hsa_circ_187956,RMVar_hsa_circ_308003,RMVar_hsa_circ_279444 42551 RMVar_ID_42551 Human_SNP_ID_634905797 A-to-I Human chr17 + 82477583 82477583 82477583 CATCCAAGCTTGGAGAGCAGTGATGCAATCATAGCTGACTCCAGCCTCGAACTCCTGGGCTCAAA CATCCAAGCTTGGAGAGCAGTGATGCAATCATGGCTGACTCCAGCCTCGAACTCCTGGGCTCAAA A G NARF Ensembl:ENSG00000141562 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1456096057 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1185286 RMVar_hsa_circ_49518,RMVar_hsa_circ_348079,RMVar_hsa_circ_330565,RMVar_hsa_circ_187956,RMVar_hsa_circ_308003,RMVar_hsa_circ_279444 42552 RMVar_ID_42552 Human_SNP_ID_634905807 A-to-I Human chr17 + 82477648 82477648 82477648 GCCATCCTCCTGCCTCAGTCTCCCAAGTAGCTAGGACTACAGGTGTGCACCACCACGCCTGGATG GCCATCCTCCTGCCTCAGTCTCCCAAGTAGCTGGGACTACAGGTGTGCACCACCACGCCTGGATG A G NARF Ensembl:ENSG00000141562 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1355938684 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49518,RMVar_hsa_circ_348079,RMVar_hsa_circ_330565,RMVar_hsa_circ_187956,RMVar_hsa_circ_308003,RMVar_hsa_circ_279444 42553 RMVar_ID_42553 Human_SNP_ID_634905822 A-to-I Human chr17 + 82477703 82477702 82477704 CGCCTGGATGATTTTTTTATTTTTCTAGAGACAGAGTCTCACCGTGTTGCCTAGGCTGGTCTTGA CGCCTGGATGATTTTTTTATTTTTCTAGAGAC__AGTCTCACCGTGTTGCCTAGGCTGGTCTTGA CAG C NARF Ensembl:ENSG00000141562 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1159531303 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_49518,RMVar_hsa_circ_348079,RMVar_hsa_circ_330565,RMVar_hsa_circ_187956,RMVar_hsa_circ_308003,RMVar_hsa_circ_279444 42554 RMVar_ID_42554 Human_SNP_ID_634907462 A-to-I Human chr17 + 82482870 82482870 82482870 CAGGCTCTGCAGTGGCTCCATCTTGGCTCACTACAACCTCCGCGCCTCCTAGGATCAAGCGATTC CAGGCTCTGCAGTGGCTCCATCTTGGCTCACTGCAACCTCCGCGCCTCCTAGGATCAAGCGATTC A G NARF,NARF-IT1 Ensembl:ENSG00000141562,Ensembl:ENSG00000266236 Protein coding,lincRNA intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1425721986 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_279444 42555 RMVar_ID_42555 Human_SNP_ID_634907482 A-to-I Human chr17 + 82482924 82482924 82482924 TCAAGCGATTCTCCTCCCTCAGCCTCCCGAGTAGCTGGGATTACAGGTGCGCCCCACCACACCAG TCAAGCGATTCTCCTCCCTCAGCCTCCCGAGTGGCTGGGATTACAGGTGCGCCCCACCACACCAG A G NARF,NARF-IT1 Ensembl:ENSG00000141562,Ensembl:ENSG00000266236 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1007040038 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_279444 42556 RMVar_ID_42556 Human_SNP_ID_634907571 A-to-I Human chr17 + 82483212 82483212 82483212 GTGGTAGTGCACACCTGTAATCACAGCTACTCAGGAGGCTGCGGCAAGAGAATCACTTGAACCCG GTGGTAGTGCACACCTGTAATCACAGCTACTCGGGAGGCTGCGGCAAGAGAATCACTTGAACCCG A G NARF,NARF-IT1 Ensembl:ENSG00000141562,Ensembl:ENSG00000266236 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs962574053 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1885932,Human_Splice_Rec_1885933,Human_Splice_Rec_1885945,Human_Splice_Rec_1885964,Human_Splice_Rec_1885965 RMVar_hsa_circ_279444,RMVar_hsa_circ_101494,RMVar_hsa_circ_187958 42557 RMVar_ID_42557 Human_SNP_ID_634909031 A-to-I Human chr17 + 82488066 82488066 82488066 ACACGTGCAGGAGCTGTACCAGGAGTGGCTGGAGGGGATCAACTCCCCCAAGGCCCGAGAGGTGC ACACGTGCAGGAGCTGTACCAGGAGTGGCTGGGGGGGATCAACTCCCCCAAGGCCCGAGAGGTGC A G NARF Ensembl:ENSG00000141562 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs200355609 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_503669,Human_RBP_ID_5115003,Human_RBP_ID_5143425,Human_RBP_ID_9289580,Human_RBP_ID_17653712,Human_RBP_ID_17903460,Human_RBP_ID_18164100,Human_RBP_ID_22443282,Human_RBP_ID_27459576 42558 RMVar_ID_42558 Human_SNP_ID_634919947 A-to-I Human chr17 + 82522271 82522271 82522271 CAGTGCTCAGGAGTTTGAAGTTGCTGTGAGCTATGATTGCACCACTGCATTCCAGGCTGGGATTA CAGTGCTCAGGAGTTTGAAGTTGCTGTGAGCTGTGATTGCACCACTGCATTCCAGGCTGGGATTA A G FOXK2 Ensembl:ENSG00000141568 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1289729283 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42559 RMVar_ID_42559 Human_SNP_ID_634921633 A-to-I Human chr17 + 82527900 82527900 82527900 ATAGCTCACTGCAGCCTTGAACTCCTGGACTCAAGCGATCTTCCCACCTCAGTCTCCCGTGTAGC ATAGCTCACTGCAGCCTTGAACTCCTGGACTCGAGCGATCTTCCCACCTCAGTCTCCCGTGTAGC A G FOXK2 Ensembl:ENSG00000141568 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903678812 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42560 RMVar_ID_42560 Human_SNP_ID_634922287 A-to-I Human chr17 + 82530198 82530198 82530198 TTGACTTTCATTTGGACAGATGGAATATAGAAAACCTGAAATAGGCCGGGCACGTTGGGTCACGC TTGACTTTCATTTGGACAGATGGAATATAGAAGACCTGAAATAGGCCGGGCACGTTGGGTCACGC A G FOXK2 Ensembl:ENSG00000141568 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350197797 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1185294,Human_RBP_ID_13205993 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 42561 RMVar_ID_42561 Human_SNP_ID_634942010 A-to-I Human chr17 + 82594933 82594933 82594933 CTGTGGCGGCAGCACCTGTAGTCCCAGCCACCAAGAGGCTAAGGCAGGGAGATCGTTTGAGCCAG CTGTGGCGGCAGCACCTGTAGTCCCAGCCACCCAGAGGCTAAGGCAGGGAGATCGTTTGAGCCAG A C FOXK2 Ensembl:ENSG00000141568 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928214105 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13207974 42562 RMVar_ID_42562 Human_SNP_ID_634943381 A-to-I Human chr17 + 82599237 82599237 82599237 CTCCTGCCTCAGCCTCCCGAGTAGTTGGGACTATAGGCCCCCACCACCTTGCCCGGCTAATGTTT CTCCTGCCTCAGCCTCCCGAGTAGTTGGGACTGTAGGCCCCCACCACCTTGCCCGGCTAATGTTT A G FOXK2 Ensembl:ENSG00000141568 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1038193271 Functional Loss SNV dbSNP153 33..33 33 - - - 42563 RMVar_ID_42563 Human_SNP_ID_634950347 A-to-I Human chr17 - 82620277 82620277 82620277 GGCACCCACCGCCATGCCTGGCTAATGTTTGTATTTTTAGTAGAGACGAGGTTTCACCATGTTGG GGCACCCACCGCCATGCCTGGCTAATGTTTGTGTTTTTAGTAGAGACGAGGTTTCACCATGTTGG T C WDR45B Ensembl:ENSG00000141580 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs778660015 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42564 RMVar_ID_42564 Human_SNP_ID_634951599 A-to-I Human chr17 - 82624435 82624435 82624435 CAACGTGGTGAAACCTCATCTCTACTAAACATACAAAACTTAGCTGGATGTGGTGGCGGGTGCCC CAACGTGGTGAAACCTCATCTCTACTAAACATGCAAAACTTAGCTGGATGTGGTGGCGGGTGCCC T C WDR45B Ensembl:ENSG00000141580 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs539594067 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25332963 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_187984 42565 RMVar_ID_42565 Human_SNP_ID_634951603 A-to-I Human chr17 - 82624450 82624450 82624450 AGAGAGCATCCTGGTCAACGTGGTGAAACCTCATCTCTACTAAACATACAAAACTTAGCTGGATG AGAGAGCATCCTGGTCAACGTGGTGAAACCTCGTCTCTACTAAACATACAAAACTTAGCTGGATG T C WDR45B Ensembl:ENSG00000141580 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1190049200 Functional Loss SNV dbSNP153 33..33 33 - - - 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_187984 42566 RMVar_ID_42566 Human_SNP_ID_634951646 A-to-I Human chr17 - 82624549 82624549 82624549 TCACAGTCAAGACAGAACAGTCGGCCGGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTTTAGG TCACAGTCAAGACAGAACAGTCGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTAGG T C WDR45B Ensembl:ENSG00000141580 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1047078090 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13208745 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_187984 42567 RMVar_ID_42567 Human_SNP_ID_634952202 A-to-I Human chr17 - 82626294 82626294 82626294 TGACCTCATGATCCACCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACTGCGC TGACCTCATGATCCACCCGCCTCAGCCTCCCAGAGTGCTGGGATTACAGGTGTGAGCCACTGCGC T C WDR45B Ensembl:ENSG00000141580 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270993547 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42568 RMVar_ID_42568 Human_SNP_ID_634952225 A-to-I Human chr17 - 82626413 82626413 82626413 TTCCTGCCTCAGCCTCCGGAGTAGCTGGGACTACAGGCGCACACCACCAAGCCTGGCTGATTTTG TTCCTGCCTCAGCCTCCGGAGTAGCTGGGACTGCAGGCGCACACCACCAAGCCTGGCTGATTTTG T C WDR45B Ensembl:ENSG00000141580 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1001523306 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42569 RMVar_ID_42569 Human_SNP_ID_634952238 A-to-I Human chr17 - 82626447 82626447 82626447 TTCACTGTAACCTCTGCCTCCCGGGTTCAAGCAATTCCTGCCTCAGCCTCCGGAGTAGCTGGGAC TTCACTGTAACCTCTGCCTCCCGGGTTCAAGCGATTCCTGCCTCAGCCTCCGGAGTAGCTGGGAC T C WDR45B Ensembl:ENSG00000141580 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1206516200 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25332978 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 42570 RMVar_ID_42570 Human_SNP_ID_634952254 A-to-I Human chr17 - 82626526 82626526 82626526 TTTTTTTTTTTTTTTTTTTTTTTTTGGGAGATAGAGTCTTGCTCTGTTGCCAGACTGGAGTGCAG TTTTTTTTTTTTTTTTTTTTTTTTTGGGAGATTGAGTCTTGCTCTGTTGCCAGACTGGAGTGCAG T A WDR45B Ensembl:ENSG00000141580 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1205755617 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42571 RMVar_ID_42571 Human_SNP_ID_634952753 A-to-I Human chr17 - 82628144 82628144 82628144 TACCAAAAATACAAAACTTAGCTGGGCATGGTAGTGCATGCCTGTAGTCCCAGCCATTTGGGAAG TACCAAAAATACAAAACTTAGCTGGGCATGGTTGTGCATGCCTGTAGTCCCAGCCATTTGGGAAG T A WDR45B Ensembl:ENSG00000141580 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965447367 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42572 RMVar_ID_42572 Human_SNP_ID_634955076 A-to-I Human chr17 - 82635986 82635986 82635986 GCCTCCCGGGTTCAAGTGATTCTCCTGCCCCAACTTCTCGAGTAGCTGGGATTATAGGCATGCGC GCCTCCCGGGTTCAAGTGATTCTCCTGCCCCAGCTTCTCGAGTAGCTGGGATTATAGGCATGCGC T C WDR45B Ensembl:ENSG00000141580 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs762438496 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42573 RMVar_ID_42573 Human_SNP_ID_634955667 A-to-I Human chr17 - 82638123 82638123 82638123 GGAGTGCAGTGGCTCCATCTTGGCTCACTGCAACCTCCACCTCATGGGTTCAAGCGATTCTCGTG GGAGTGCAGTGGCTCCATCTTGGCTCACTGCAGCCTCCACCTCATGGGTTCAAGCGATTCTCGTG T C WDR45B Ensembl:ENSG00000141580 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs887080420 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42574 RMVar_ID_42574 Human_SNP_ID_634960359 A-to-I Human chr17 + 82651308 82651307 82651309 CCAGCTTAATTTTTTGTATTTTTAGTGGAGACAGGGTTTCATCATGTTGCCCAGGCTGGTCTTGA CCAGCTTAATTTTTTGTATTTTTAGTGGAGAC__GGTTTCATCATGTTGCCCAGGCTGGTCTTGA CAG C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs948923051 Functional Loss DEL dbSNP153 33..34 33 - - - 42575 RMVar_ID_42575 Human_SNP_ID_634960360 A-to-I Human chr17 + 82651308 82651308 82651308 CCAGCTTAATTTTTTGTATTTTTAGTGGAGACAGGGTTTCATCATGTTGCCCAGGCTGGTCTTGA CCAGCTTAATTTTTTGTATTTTTAGTGGAGACGGGGTTTCATCATGTTGCCCAGGCTGGTCTTGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs936798804 Functional Loss SNV dbSNP153 33..33 33 - - - 42576 RMVar_ID_42576 Human_SNP_ID_634973008 A-to-I Human chr17 - 82693131 82693131 82693131 AGGTGTGGTGGCGGGCACCTGTATTCCCAGCTACTCGGGAGACTGAGGCAGGAGAAGCACTTGAA AGGTGTGGTGGCGGGCACCTGTATTCCCAGCTGCTCGGGAGACTGAGGCAGGAGAAGCACTTGAA T C RAB40B Ensembl:ENSG00000141542 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1349489302 Functional Loss SNV dbSNP153 33..33 33 - - - 42577 RMVar_ID_42577 Human_SNP_ID_634985307 A-to-I Human chr17 + 82732934 82732934 82732934 TTTTTTTGTATTTTTCGTAGAGATAGGGTTTCACCAAGTTGATCAGGCTGGTCTTGAACTCCTGA TTTTTTTGTATTTTTCGTAGAGATAGGGTTTCGCCAAGTTGATCAGGCTGGTCTTGAACTCCTGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs964298986 Functional Loss SNV dbSNP153 33..33 33 - - - 42578 RMVar_ID_42578 Human_SNP_ID_634986681 A-to-I Human chr17 + 82737357 82737357 82737357 CATCATGGTGAAATTCCATCTCTTTTTTTTTGAGACGGACTCTTGCTCTGTCGCCCAGGCTGGAT CATCATGGTGAAATTCCATCTCTTTTTTTTTGGGACGGACTCTTGCTCTGTCGCCCAGGCTGGAT A G FN3K Ensembl:ENSG00000167363 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1402198888 Functional Loss SNV dbSNP153 33..33 33 - - - 42579 RMVar_ID_42579 Human_SNP_ID_634986789 A-to-I Human chr17 + 82737626 82737626 82737626 TTACAGGTGCGAGCCACCACGCACGGCGGTGGAACTCCATCTCTAGTAAAAATACAGAAAAACAC TTACAGGTGCGAGCCACCACGCACGGCGGTGGGACTCCATCTCTAGTAAAAATACAGAAAAACAC A G FN3K Ensembl:ENSG00000167363 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1008189681 Functional Loss SNV dbSNP153 33..33 33 - - - 42580 RMVar_ID_42580 Human_SNP_ID_635010829 A-to-I Human chr17 + 82816627 82816627 82816627 GCAATCTCTGCTCACTGTAATCTCTGCCTCCCAGGACCAGGCGATCCTCTCACCTCAGCCTCCTG GCAATCTCTGCTCACTGTAATCTCTGCCTCCCGGGACCAGGCGATCCTCTCACCTCAGCCTCCTG A G TBCD Ensembl:ENSG00000141556 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs890671458 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13210955 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 42581 RMVar_ID_42581 Human_SNP_ID_635020421 A-to-I Human chr17 + 82847132 82847132 82847132 CCAGCACTTTGGGAGGCCAAGGTGGGCGGATCATGAGGTCAGGAGATCGAGACCATCTTGTCTAA CCAGCACTTTGGGAGGCCAAGGTGGGCGGATCGTGAGGTCAGGAGATCGAGACCATCTTGTCTAA A G TBCD Ensembl:ENSG00000141556 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1028437360 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42582 RMVar_ID_42582 Human_SNP_ID_635020426 A-to-I Human chr17 + 82847140 82847140 82847140 TTGGGAGGCCAAGGTGGGCGGATCATGAGGTCAGGAGATCGAGACCATCTTGTCTAACACAGTGA TTGGGAGGCCAAGGTGGGCGGATCATGAGGTCGGGAGATCGAGACCATCTTGTCTAACACAGTGA A G TBCD Ensembl:ENSG00000141556 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1201068426 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42583 RMVar_ID_42583 Human_SNP_ID_635020441 A-to-I Human chr17 + 82847163 82847163 82847163 CATGAGGTCAGGAGATCGAGACCATCTTGTCTAACACAGTGAAACCCCGTCTCTACTAAAAATAC CATGAGGTCAGGAGATCGAGACCATCTTGTCTCACACAGTGAAACCCCGTCTCTACTAAAAATAC A C TBCD Ensembl:ENSG00000141556 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1459724990 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42584 RMVar_ID_42584 Human_SNP_ID_635020442 A-to-I Human chr17 + 82847168 82847168 82847168 GGTCAGGAGATCGAGACCATCTTGTCTAACACAGTGAAACCCCGTCTCTACTAAAAATACACAAA GGTCAGGAGATCGAGACCATCTTGTCTAACACGGTGAAACCCCGTCTCTACTAAAAATACACAAA A G TBCD Ensembl:ENSG00000141556 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs543022894 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42585 RMVar_ID_42585 Human_SNP_ID_635020443 A-to-I Human chr17 + 82847168 82847168 82847168 GGTCAGGAGATCGAGACCATCTTGTCTAACACAGTGAAACCCCGTCTCTACTAAAAATACACAAA GGTCAGGAGATCGAGACCATCTTGTCTAACACTGTGAAACCCCGTCTCTACTAAAAATACACAAA A T TBCD Ensembl:ENSG00000141556 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs543022894 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42586 RMVar_ID_42586 Human_SNP_ID_635020446 A-to-I Human chr17 + 82847172 82847172 82847172 AGGAGATCGAGACCATCTTGTCTAACACAGTGAAACCCCGTCTCTACTAAAAATACACAAAAAAT AGGAGATCGAGACCATCTTGTCTAACACAGTGGAACCCCGTCTCTACTAAAAATACACAAAAAAT A G TBCD Ensembl:ENSG00000141556 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs181645955 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42587 RMVar_ID_42587 Human_SNP_ID_635020489 A-to-I Human chr17 + 82847259 82847259 82847259 CCTGTAATCCCAACTACTCGGGAGGCTGAGGCAGGAGAATGGTGTGAACCTGGGAGGCGGAGCTT CCTGTAATCCCAACTACTCGGGAGGCTGAGGCGGGAGAATGGTGTGAACCTGGGAGGCGGAGCTT A G TBCD Ensembl:ENSG00000141556 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs763979903 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42588 RMVar_ID_42588 Human_SNP_ID_635020490 A-to-I Human chr17 + 82847259 82847259 82847259 CCTGTAATCCCAACTACTCGGGAGGCTGAGGCAGGAGAATGGTGTGAACCTGGGAGGCGGAGCTT CCTGTAATCCCAACTACTCGGGAGGCTGAGGCTGGAGAATGGTGTGAACCTGGGAGGCGGAGCTT A T TBCD Ensembl:ENSG00000141556 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs763979903 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42589 RMVar_ID_42589 Human_SNP_ID_635047326 A-to-I Human chr17 + 82933374 82933374 82933374 ACAGCTCACTGCAGCCTCTACCTCAGCCTCCCAAGTATCTGGGACTACAGGCATGCGCTGTAGTC ACAGCTCACTGCAGCCTCTACCTCAGCCTCCCTAGTATCTGGGACTACAGGCATGCGCTGTAGTC A T TBCD Ensembl:ENSG00000141556 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1196832935 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13212796 RMVar_hsa_circ_93164,RMVar_hsa_circ_187988,RMVar_hsa_circ_110214,RMVar_hsa_circ_81315,RMVar_hsa_circ_78452,RMVar_hsa_circ_188017,RMVar_hsa_circ_188018,RMVar_hsa_circ_188016,RMVar_hsa_circ_109124,RMVar_hsa_circ_188050,RMVar_hsa_circ_123126,RMVar_hsa_circ_188072,RMVar_hsa_circ_111699,RMVar_hsa_circ_188084,RMVar_hsa_circ_58549,RMVar_hsa_circ_104603,RMVar_hsa_circ_188116,RMVar_hsa_circ_111306,RMVar_hsa_circ_104022,RMVar_hsa_circ_108563,RMVar_hsa_circ_94322,RMVar_hsa_circ_188137,RMVar_hsa_circ_188135,RMVar_hsa_circ_188136,RMVar_hsa_circ_188134,RMVar_hsa_circ_109452,RMVar_hsa_circ_188151 42590 RMVar_ID_42590 Human_SNP_ID_495582607 A-to-I Human chr12 - 30676069 30676069 30676069 GTAAAGAAAAAAGAAAAATAGCTAGATGTGGTAGCATGTGCCAGCTACTTGGGAAGCTGAGGTGG GTAAAGAAAAAAGAAAAATAGCTAGATGTGGTGGCATGTGCCAGCTACTTGGGAAGCTGAGGTGG T C IPO8 Ensembl:ENSG00000133704 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1473132100 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5786,RMVar_hsa_circ_268889,RMVar_hsa_circ_67900,RMVar_hsa_circ_289876,RMVar_hsa_circ_36521,RMVar_hsa_circ_47677,RMVar_hsa_circ_61987,RMVar_hsa_circ_62165,RMVar_hsa_circ_360417,RMVar_hsa_circ_15776,RMVar_hsa_circ_41776,RMVar_hsa_circ_349753,RMVar_hsa_circ_155609,RMVar_hsa_circ_350102,RMVar_hsa_circ_328831,RMVar_hsa_circ_155611,RMVar_hsa_circ_155612,RMVar_hsa_circ_367877,RMVar_hsa_circ_41562,RMVar_hsa_circ_97460,RMVar_hsa_circ_45328,RMVar_hsa_circ_53162,RMVar_hsa_circ_64284,RMVar_hsa_circ_155615,RMVar_hsa_circ_296875,RMVar_hsa_circ_324734,RMVar_hsa_circ_284576,RMVar_hsa_circ_155617,RMVar_hsa_circ_155618,RMVar_hsa_circ_155616,RMVar_hsa_circ_292429,RMVar_hsa_circ_65594,RMVar_hsa_circ_329322,RMVar_hsa_circ_155619,RMVar_hsa_circ_155620 42591 RMVar_ID_42591 Human_SNP_ID_495584701 A-to-I Human chr12 - 30685840 30685840 30685840 GCAGTGCTGTGGCATGATCTCAGCTCACTGCAACCTCCGCCTCCTGGGTTCAAGGAATTTGCTGG GCAGTGCTGTGGCATGATCTCAGCTCACTGCAGCCTCCGCCTCCTGGGTTCAAGGAATTTGCTGG T C IPO8 Ensembl:ENSG00000133704 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1181326249 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5786,RMVar_hsa_circ_67900,RMVar_hsa_circ_47677,RMVar_hsa_circ_61987,RMVar_hsa_circ_360417,RMVar_hsa_circ_349753,RMVar_hsa_circ_155612,RMVar_hsa_circ_45328,RMVar_hsa_circ_64284,RMVar_hsa_circ_284576,RMVar_hsa_circ_155618,RMVar_hsa_circ_65594,RMVar_hsa_circ_285375,RMVar_hsa_circ_325895 42592 RMVar_ID_42592 Human_SNP_ID_495667815 A-to-I Human chr12 - 31035062 31035062 31035062 GGAGTCTCTCTATGTTGCCCAGGCTGGTCTCAAACTCCTGGCCTCCAGCGATCTGCCTGCCTCAG GGAGTCTCTCTATGTTGCCCAGGCTGGTCTCAGACTCCTGGCCTCCAGCGATCTGCCTGCCTCAG T C DDX11-AS1 Ensembl:ENSG00000245614 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1485105945 Functional Loss SNV dbSNP153 33..33 33 - - - 42593 RMVar_ID_42593 Human_SNP_ID_495732396 A-to-I Human chr12 - 31282510 31282510 31282510 TCAAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGTTTATAGGTGCCCGCCACCAGACCCG TCAAGTGATTCTCCTGCCTCAGCCTCCCAAGTGGCTGGGTTTATAGGTGCCCGCCACCAGACCCG T C SINHCAF Ensembl:ENSG00000139146 Protein coding exon GSE38233;GSE99789 cultured B-cells;esophageal squamous carcinoma cells,EC109 - 24183664,29796672 RNA-Seq:(High) rs547472707 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_418248,Human_RBP_ID_23556169 42594 RMVar_ID_42594 Human_SNP_ID_495732402 A-to-I Human chr12 - 31282539 31282539 31282539 TGGCTCACTGCAACTTCCGTCTCCCGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGCT TGGCTCACTGCAACTTCCGTCTCCCGGGTTCAGGTGATTCTCCTGCCTCAGCCTCCCAAGTAGCT T C SINHCAF Ensembl:ENSG00000139146 Protein coding exon GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs1341480152 Functional Loss SNV dbSNP153 33..33 33 - - - 42595 RMVar_ID_42595 Human_SNP_ID_495735863 A-to-I Human chr12 - 31296254 31296254 31296254 GGCTGAGGTGGGAGGATCACTTGAACCTGGGAAGTTGAGGCTGCAGTGAGCCATAATCCCACCAC GGCTGAGGTGGGAGGATCACTTGAACCTGGGAGGTTGAGGCTGCAGTGAGCCATAATCCCACCAC T C SINHCAF Ensembl:ENSG00000139146 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1245957467 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24646,RMVar_hsa_circ_336553,RMVar_hsa_circ_358762,RMVar_hsa_circ_353477 42596 RMVar_ID_42596 Human_SNP_ID_495735882 A-to-I Human chr12 - 31296326 31296326 31296326 CCCTGTCTCTACAAAAAATACAAAAATTAGCCAGGCGTGGTGGCACGTGCCTGTGGTCCCAGCTA CCCTGTCTCTACAAAAAATACAAAAATTAGCCGGGCGTGGTGGCACGTGCCTGTGGTCCCAGCTA T C SINHCAF Ensembl:ENSG00000139146 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1210916008 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24646,RMVar_hsa_circ_336553,RMVar_hsa_circ_358762,RMVar_hsa_circ_353477 42597 RMVar_ID_42597 Human_SNP_ID_495735963 A-to-I Human chr12 - 31296688 31296688 31296688 ACCATGCCCTGCTAATTTTTCTATTTTTTTGTAGATACAGGATTTTGCCATGTTGCCCAGGCTGG ACCATGCCCTGCTAATTTTTCTATTTTTTTGTGGATACAGGATTTTGCCATGTTGCCCAGGCTGG T C SINHCAF Ensembl:ENSG00000139146 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1337054453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11923512 RMVar_hsa_circ_24646,RMVar_hsa_circ_336553,RMVar_hsa_circ_358762,RMVar_hsa_circ_353477 42598 RMVar_ID_42598 Human_SNP_ID_495769042 A-to-I Human chr12 - 31426398 31426398 31426398 TTTTAGAAATATATGCAAGAGGCACGAAGTTTAGGAAAAAACCTGAGGCAACCCAAACTGTCAGA TTTTAGAAATATATGCAAGAGGCACGAAGTTTGGGAAAAAACCTGAGGCAACCCAAACTGTCAGA T C DENND5B Ensembl:ENSG00000170456 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs763366064 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1352674,Human_Splice_Rec_1352718 RMVar_hsa_circ_125954,RMVar_hsa_circ_113567,RMVar_hsa_circ_14008,RMVar_hsa_circ_307970,RMVar_hsa_circ_364709,RMVar_hsa_circ_155650,RMVar_hsa_circ_343047,RMVar_hsa_circ_307882,RMVar_hsa_circ_155654,RMVar_hsa_circ_155653,RMVar_hsa_circ_306219,RMVar_hsa_circ_63807,RMVar_hsa_circ_155659,RMVar_hsa_circ_71388,RMVar_hsa_circ_155661,RMVar_hsa_circ_378553,RMVar_hsa_circ_367921,RMVar_hsa_circ_276642,RMVar_hsa_circ_271833,RMVar_hsa_circ_37399,RMVar_hsa_circ_75304,RMVar_hsa_circ_42970,RMVar_hsa_circ_155662,RMVar_hsa_circ_155664,RMVar_hsa_circ_155663,RMVar_hsa_circ_340172,RMVar_hsa_circ_374744,RMVar_hsa_circ_378213,RMVar_hsa_circ_365848,RMVar_hsa_circ_282155,RMVar_hsa_circ_267913,RMVar_hsa_circ_155671,RMVar_hsa_circ_155672,RMVar_hsa_circ_155670,RMVar_hsa_circ_293923,RMVar_hsa_circ_297600,RMVar_hsa_circ_64677,RMVar_hsa_circ_155677,RMVar_hsa_circ_297211,RMVar_hsa_circ_155675,RMVar_hsa_circ_1750,RMVar_hsa_circ_155674,RMVar_hsa_circ_325036,RMVar_hsa_circ_338352,RMVar_hsa_circ_358826,RMVar_hsa_circ_292469,RMVar_hsa_circ_22495,RMVar_hsa_circ_155679,RMVar_hsa_circ_155678,RMVar_hsa_circ_155682,RMVar_hsa_circ_16858,RMVar_hsa_circ_328959,RMVar_hsa_circ_334634,RMVar_hsa_circ_155676,RMVar_hsa_circ_334258,RMVar_hsa_circ_285435,RMVar_hsa_circ_155683,RMVar_hsa_circ_155684,RMVar_hsa_circ_285776,RMVar_hsa_circ_348467,RMVar_hsa_circ_370799,RMVar_hsa_circ_289916,RMVar_hsa_circ_272828,RMVar_hsa_circ_273783,RMVar_hsa_circ_53381,RMVar_hsa_circ_108234,RMVar_hsa_circ_155688,RMVar_hsa_circ_155690,RMVar_hsa_circ_155691,RMVar_hsa_circ_155692,RMVar_hsa_circ_155689,RMVar_hsa_circ_155687,RMVar_hsa_circ_155693,RMVar_hsa_circ_68936,RMVar_hsa_circ_106393,RMVar_hsa_circ_155694,RMVar_hsa_circ_285423,RMVar_hsa_circ_288129,RMVar_hsa_circ_297027,RMVar_hsa_circ_103856,RMVar_hsa_circ_155695,RMVar_hsa_circ_155697,RMVar_hsa_circ_155698,RMVar_hsa_circ_155696 42599 RMVar_ID_42599 Human_SNP_ID_495771471 A-to-I Human chr12 - 31435994 31435994 31435994 CAGGAGTTCAAGACTGATCTAGGCAACATGGTAAAACCCTGTCTCTACAAAAAATACAAAAATTA CAGGAGTTCAAGACTGATCTAGGCAACATGGTGAAACCCTGTCTCTACAAAAAATACAAAAATTA T C DENND5B Ensembl:ENSG00000170456 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1565576214 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113567,RMVar_hsa_circ_307970,RMVar_hsa_circ_364709,RMVar_hsa_circ_155654,RMVar_hsa_circ_155653,RMVar_hsa_circ_306219,RMVar_hsa_circ_155659,RMVar_hsa_circ_71388,RMVar_hsa_circ_155661,RMVar_hsa_circ_378553,RMVar_hsa_circ_276642,RMVar_hsa_circ_37399,RMVar_hsa_circ_75304,RMVar_hsa_circ_155662,RMVar_hsa_circ_340172,RMVar_hsa_circ_374744,RMVar_hsa_circ_378213,RMVar_hsa_circ_267913,RMVar_hsa_circ_155672,RMVar_hsa_circ_297600,RMVar_hsa_circ_64677,RMVar_hsa_circ_155677,RMVar_hsa_circ_155675,RMVar_hsa_circ_325036,RMVar_hsa_circ_338352,RMVar_hsa_circ_358826,RMVar_hsa_circ_22495,RMVar_hsa_circ_16858,RMVar_hsa_circ_155676,RMVar_hsa_circ_334258,RMVar_hsa_circ_285435,RMVar_hsa_circ_155683,RMVar_hsa_circ_155684,RMVar_hsa_circ_285776,RMVar_hsa_circ_348467,RMVar_hsa_circ_370799,RMVar_hsa_circ_272828,RMVar_hsa_circ_53381,RMVar_hsa_circ_108234,RMVar_hsa_circ_155690,RMVar_hsa_circ_155691,RMVar_hsa_circ_155692,RMVar_hsa_circ_155689,RMVar_hsa_circ_155693,RMVar_hsa_circ_68936,RMVar_hsa_circ_285423,RMVar_hsa_circ_288129,RMVar_hsa_circ_103856,RMVar_hsa_circ_65615,RMVar_hsa_circ_155699,RMVar_hsa_circ_155697,RMVar_hsa_circ_155698,RMVar_hsa_circ_155696,RMVar_hsa_circ_76005,RMVar_hsa_circ_286705,RMVar_hsa_circ_348459,RMVar_hsa_circ_367473,RMVar_hsa_circ_301220,RMVar_hsa_circ_274768,RMVar_hsa_circ_155700,RMVar_hsa_circ_155701,RMVar_hsa_circ_155702 42600 RMVar_ID_42600 Human_SNP_ID_495772471 A-to-I Human chr12 - 31439700 31439700 31439700 GTCTAGAAATCCTGACCTCAGGTTATCCGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGC GTCTAGAAATCCTGACCTCAGGTTATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGC T C DENND5B Ensembl:ENSG00000170456 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs915567871 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113567,RMVar_hsa_circ_307970,RMVar_hsa_circ_364709,RMVar_hsa_circ_155654,RMVar_hsa_circ_155653,RMVar_hsa_circ_306219,RMVar_hsa_circ_155659,RMVar_hsa_circ_71388,RMVar_hsa_circ_155661,RMVar_hsa_circ_378553,RMVar_hsa_circ_276642,RMVar_hsa_circ_37399,RMVar_hsa_circ_75304,RMVar_hsa_circ_155662,RMVar_hsa_circ_340172,RMVar_hsa_circ_374744,RMVar_hsa_circ_378213,RMVar_hsa_circ_267913,RMVar_hsa_circ_155672,RMVar_hsa_circ_297600,RMVar_hsa_circ_64677,RMVar_hsa_circ_155677,RMVar_hsa_circ_155675,RMVar_hsa_circ_325036,RMVar_hsa_circ_338352,RMVar_hsa_circ_358826,RMVar_hsa_circ_22495,RMVar_hsa_circ_16858,RMVar_hsa_circ_155676,RMVar_hsa_circ_334258,RMVar_hsa_circ_285435,RMVar_hsa_circ_155683,RMVar_hsa_circ_155684,RMVar_hsa_circ_285776,RMVar_hsa_circ_348467,RMVar_hsa_circ_370799,RMVar_hsa_circ_272828,RMVar_hsa_circ_53381,RMVar_hsa_circ_108234,RMVar_hsa_circ_155690,RMVar_hsa_circ_155691,RMVar_hsa_circ_155692,RMVar_hsa_circ_155689,RMVar_hsa_circ_155693,RMVar_hsa_circ_68936,RMVar_hsa_circ_285423,RMVar_hsa_circ_288129,RMVar_hsa_circ_103856,RMVar_hsa_circ_65615,RMVar_hsa_circ_155699,RMVar_hsa_circ_155697,RMVar_hsa_circ_155698,RMVar_hsa_circ_155696,RMVar_hsa_circ_76005,RMVar_hsa_circ_286705,RMVar_hsa_circ_348459,RMVar_hsa_circ_367473,RMVar_hsa_circ_301220,RMVar_hsa_circ_274768,RMVar_hsa_circ_155700,RMVar_hsa_circ_155701,RMVar_hsa_circ_155702 42601 RMVar_ID_42601 Human_SNP_ID_495772778 A-to-I Human chr12 - 31440767 31440767 31440767 CCAGCTACTGGTGAGGCTTAGGTGGGAGGATCACTTGAACCTGAGAGGTCTAGGCTGCAGTGAGC CCAGCTACTGGTGAGGCTTAGGTGGGAGGATCGCTTGAACCTGAGAGGTCTAGGCTGCAGTGAGC T C DENND5B Ensembl:ENSG00000170456 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs375876936 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113567,RMVar_hsa_circ_307970,RMVar_hsa_circ_364709,RMVar_hsa_circ_155654,RMVar_hsa_circ_155653,RMVar_hsa_circ_306219,RMVar_hsa_circ_155659,RMVar_hsa_circ_71388,RMVar_hsa_circ_155661,RMVar_hsa_circ_378553,RMVar_hsa_circ_276642,RMVar_hsa_circ_37399,RMVar_hsa_circ_75304,RMVar_hsa_circ_155662,RMVar_hsa_circ_340172,RMVar_hsa_circ_374744,RMVar_hsa_circ_378213,RMVar_hsa_circ_267913,RMVar_hsa_circ_155672,RMVar_hsa_circ_297600,RMVar_hsa_circ_64677,RMVar_hsa_circ_155677,RMVar_hsa_circ_155675,RMVar_hsa_circ_325036,RMVar_hsa_circ_338352,RMVar_hsa_circ_358826,RMVar_hsa_circ_22495,RMVar_hsa_circ_16858,RMVar_hsa_circ_155676,RMVar_hsa_circ_334258,RMVar_hsa_circ_285435,RMVar_hsa_circ_155683,RMVar_hsa_circ_155684,RMVar_hsa_circ_285776,RMVar_hsa_circ_348467,RMVar_hsa_circ_370799,RMVar_hsa_circ_272828,RMVar_hsa_circ_53381,RMVar_hsa_circ_108234,RMVar_hsa_circ_155690,RMVar_hsa_circ_155691,RMVar_hsa_circ_155692,RMVar_hsa_circ_155689,RMVar_hsa_circ_155693,RMVar_hsa_circ_68936,RMVar_hsa_circ_285423,RMVar_hsa_circ_288129,RMVar_hsa_circ_103856,RMVar_hsa_circ_65615,RMVar_hsa_circ_155699,RMVar_hsa_circ_155697,RMVar_hsa_circ_155698,RMVar_hsa_circ_155696,RMVar_hsa_circ_76005,RMVar_hsa_circ_286705,RMVar_hsa_circ_348459,RMVar_hsa_circ_367473,RMVar_hsa_circ_301220,RMVar_hsa_circ_274768,RMVar_hsa_circ_155700,RMVar_hsa_circ_155701,RMVar_hsa_circ_155702 42602 RMVar_ID_42602 Human_SNP_ID_495772869 A-to-I Human chr12 - 31441171 31441169 31441171 CCTAGCTAATTTTTGTATTTTTTTATAGAGACAGGATTTTGCCTTATTGCCCAAGCTGGTGTTGA CCTAGCTAATTTTTGTATTTTTTTATAGAGAC__GATTTTGCCTTATTGCCCAAGCTGGTGTTGA CCT C DENND5B Ensembl:ENSG00000170456 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917897726 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_113567,RMVar_hsa_circ_307970,RMVar_hsa_circ_364709,RMVar_hsa_circ_155654,RMVar_hsa_circ_155653,RMVar_hsa_circ_306219,RMVar_hsa_circ_155659,RMVar_hsa_circ_71388,RMVar_hsa_circ_155661,RMVar_hsa_circ_378553,RMVar_hsa_circ_276642,RMVar_hsa_circ_37399,RMVar_hsa_circ_75304,RMVar_hsa_circ_155662,RMVar_hsa_circ_340172,RMVar_hsa_circ_374744,RMVar_hsa_circ_378213,RMVar_hsa_circ_267913,RMVar_hsa_circ_155672,RMVar_hsa_circ_297600,RMVar_hsa_circ_64677,RMVar_hsa_circ_155677,RMVar_hsa_circ_155675,RMVar_hsa_circ_325036,RMVar_hsa_circ_338352,RMVar_hsa_circ_358826,RMVar_hsa_circ_22495,RMVar_hsa_circ_16858,RMVar_hsa_circ_155676,RMVar_hsa_circ_334258,RMVar_hsa_circ_285435,RMVar_hsa_circ_155683,RMVar_hsa_circ_155684,RMVar_hsa_circ_285776,RMVar_hsa_circ_348467,RMVar_hsa_circ_370799,RMVar_hsa_circ_272828,RMVar_hsa_circ_53381,RMVar_hsa_circ_108234,RMVar_hsa_circ_155690,RMVar_hsa_circ_155691,RMVar_hsa_circ_155692,RMVar_hsa_circ_155689,RMVar_hsa_circ_155693,RMVar_hsa_circ_68936,RMVar_hsa_circ_285423,RMVar_hsa_circ_288129,RMVar_hsa_circ_103856,RMVar_hsa_circ_65615,RMVar_hsa_circ_155699,RMVar_hsa_circ_155697,RMVar_hsa_circ_155698,RMVar_hsa_circ_155696,RMVar_hsa_circ_76005,RMVar_hsa_circ_286705,RMVar_hsa_circ_348459,RMVar_hsa_circ_367473,RMVar_hsa_circ_301220,RMVar_hsa_circ_274768,RMVar_hsa_circ_155700,RMVar_hsa_circ_155701,RMVar_hsa_circ_155702 42603 RMVar_ID_42603 Human_SNP_ID_495772910 A-to-I Human chr12 - 31441338 31441338 31441338 TACAAAAAAATACATACATTTTTTTTGAGACAAGGTCTTGCTCTGTTGCCCAGGCTGGAGTGCTG TACAAAAAAATACATACATTTTTTTTGAGACATGGTCTTGCTCTGTTGCCCAGGCTGGAGTGCTG T A DENND5B Ensembl:ENSG00000170456 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1267263716 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113567,RMVar_hsa_circ_307970,RMVar_hsa_circ_364709,RMVar_hsa_circ_155654,RMVar_hsa_circ_155653,RMVar_hsa_circ_306219,RMVar_hsa_circ_155659,RMVar_hsa_circ_71388,RMVar_hsa_circ_155661,RMVar_hsa_circ_378553,RMVar_hsa_circ_276642,RMVar_hsa_circ_37399,RMVar_hsa_circ_75304,RMVar_hsa_circ_155662,RMVar_hsa_circ_340172,RMVar_hsa_circ_374744,RMVar_hsa_circ_378213,RMVar_hsa_circ_267913,RMVar_hsa_circ_155672,RMVar_hsa_circ_297600,RMVar_hsa_circ_64677,RMVar_hsa_circ_155677,RMVar_hsa_circ_155675,RMVar_hsa_circ_325036,RMVar_hsa_circ_338352,RMVar_hsa_circ_358826,RMVar_hsa_circ_22495,RMVar_hsa_circ_16858,RMVar_hsa_circ_155676,RMVar_hsa_circ_334258,RMVar_hsa_circ_285435,RMVar_hsa_circ_155683,RMVar_hsa_circ_155684,RMVar_hsa_circ_285776,RMVar_hsa_circ_348467,RMVar_hsa_circ_370799,RMVar_hsa_circ_272828,RMVar_hsa_circ_53381,RMVar_hsa_circ_108234,RMVar_hsa_circ_155690,RMVar_hsa_circ_155691,RMVar_hsa_circ_155692,RMVar_hsa_circ_155689,RMVar_hsa_circ_155693,RMVar_hsa_circ_68936,RMVar_hsa_circ_285423,RMVar_hsa_circ_288129,RMVar_hsa_circ_103856,RMVar_hsa_circ_65615,RMVar_hsa_circ_155699,RMVar_hsa_circ_155697,RMVar_hsa_circ_155698,RMVar_hsa_circ_155696,RMVar_hsa_circ_76005,RMVar_hsa_circ_286705,RMVar_hsa_circ_348459,RMVar_hsa_circ_367473,RMVar_hsa_circ_301220,RMVar_hsa_circ_274768,RMVar_hsa_circ_155700,RMVar_hsa_circ_155701,RMVar_hsa_circ_155702 42604 RMVar_ID_42604 Human_SNP_ID_495773906 A-to-I Human chr12 - 31445532 31445532 31445532 CCTGGCTAATTTTTTGTATTTTTGGTAGAGACAGGGATTCACGATGTTGCTCAGGCTGGTCTTGA CCTGGCTAATTTTTTGTATTTTTGGTAGAGACTGGGATTCACGATGTTGCTCAGGCTGGTCTTGA T A DENND5B Ensembl:ENSG00000170456 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1339114770 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11924034 RMVar_hsa_circ_113567,RMVar_hsa_circ_307970,RMVar_hsa_circ_155654,RMVar_hsa_circ_306219,RMVar_hsa_circ_155659,RMVar_hsa_circ_71388,RMVar_hsa_circ_155661,RMVar_hsa_circ_276642,RMVar_hsa_circ_37399,RMVar_hsa_circ_69973,RMVar_hsa_circ_75304,RMVar_hsa_circ_155662,RMVar_hsa_circ_340172,RMVar_hsa_circ_374744,RMVar_hsa_circ_267913,RMVar_hsa_circ_155672,RMVar_hsa_circ_297600,RMVar_hsa_circ_64677,RMVar_hsa_circ_155677,RMVar_hsa_circ_155675,RMVar_hsa_circ_325036,RMVar_hsa_circ_338352,RMVar_hsa_circ_358826,RMVar_hsa_circ_22495,RMVar_hsa_circ_16858,RMVar_hsa_circ_155676,RMVar_hsa_circ_285435,RMVar_hsa_circ_155684,RMVar_hsa_circ_348467,RMVar_hsa_circ_370799,RMVar_hsa_circ_272828,RMVar_hsa_circ_53381,RMVar_hsa_circ_155690,RMVar_hsa_circ_155691,RMVar_hsa_circ_155692,RMVar_hsa_circ_68936,RMVar_hsa_circ_285423,RMVar_hsa_circ_103856,RMVar_hsa_circ_65615,RMVar_hsa_circ_155699,RMVar_hsa_circ_155697,RMVar_hsa_circ_155698,RMVar_hsa_circ_76005,RMVar_hsa_circ_348459,RMVar_hsa_circ_367473,RMVar_hsa_circ_301220,RMVar_hsa_circ_274768,RMVar_hsa_circ_283282,RMVar_hsa_circ_155701,RMVar_hsa_circ_155702,RMVar_hsa_circ_291255,RMVar_hsa_circ_340953,RMVar_hsa_circ_275975,RMVar_hsa_circ_278654,RMVar_hsa_circ_89244,RMVar_hsa_circ_155703,RMVar_hsa_circ_155705,RMVar_hsa_circ_155706,RMVar_hsa_circ_155707,RMVar_hsa_circ_155704 42605 RMVar_ID_42605 Human_SNP_ID_495773972 A-to-I Human chr12 - 31445765 31445765 31445765 GTTGGTCTTGAACTCCTGGGCTTAAGTGATCCACCTGCTTCAGTTTCCTAAAGTGCTGGGATTAC GTTGGTCTTGAACTCCTGGGCTTAAGTGATCCCCCTGCTTCAGTTTCCTAAAGTGCTGGGATTAC T G DENND5B Ensembl:ENSG00000170456 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1169592559 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113567,RMVar_hsa_circ_307970,RMVar_hsa_circ_155654,RMVar_hsa_circ_306219,RMVar_hsa_circ_155659,RMVar_hsa_circ_71388,RMVar_hsa_circ_155661,RMVar_hsa_circ_276642,RMVar_hsa_circ_37399,RMVar_hsa_circ_69973,RMVar_hsa_circ_75304,RMVar_hsa_circ_155662,RMVar_hsa_circ_340172,RMVar_hsa_circ_374744,RMVar_hsa_circ_267913,RMVar_hsa_circ_155672,RMVar_hsa_circ_297600,RMVar_hsa_circ_64677,RMVar_hsa_circ_155677,RMVar_hsa_circ_155675,RMVar_hsa_circ_325036,RMVar_hsa_circ_338352,RMVar_hsa_circ_358826,RMVar_hsa_circ_22495,RMVar_hsa_circ_16858,RMVar_hsa_circ_155676,RMVar_hsa_circ_285435,RMVar_hsa_circ_155684,RMVar_hsa_circ_348467,RMVar_hsa_circ_370799,RMVar_hsa_circ_272828,RMVar_hsa_circ_53381,RMVar_hsa_circ_155690,RMVar_hsa_circ_155691,RMVar_hsa_circ_155692,RMVar_hsa_circ_68936,RMVar_hsa_circ_285423,RMVar_hsa_circ_103856,RMVar_hsa_circ_65615,RMVar_hsa_circ_155699,RMVar_hsa_circ_155697,RMVar_hsa_circ_155698,RMVar_hsa_circ_76005,RMVar_hsa_circ_348459,RMVar_hsa_circ_367473,RMVar_hsa_circ_301220,RMVar_hsa_circ_274768,RMVar_hsa_circ_283282,RMVar_hsa_circ_155701,RMVar_hsa_circ_155702,RMVar_hsa_circ_291255,RMVar_hsa_circ_340953,RMVar_hsa_circ_275975,RMVar_hsa_circ_278654,RMVar_hsa_circ_89244,RMVar_hsa_circ_155703,RMVar_hsa_circ_155705,RMVar_hsa_circ_155706,RMVar_hsa_circ_155707,RMVar_hsa_circ_155704 42606 RMVar_ID_42606 Human_SNP_ID_495773990 A-to-I Human chr12 - 31445851 31445851 31445851 GCATGTGCCACCACCCTCGGGTAATTTTTTGTATTTTTTGTAGAGACAGGGTTTCACCATGTTGC GCATGTGCCACCACCCTCGGGTAATTTTTTGTGTTTTTTGTAGAGACAGGGTTTCACCATGTTGC T C DENND5B Ensembl:ENSG00000170456 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1005056655 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11924039 RMVar_hsa_circ_113567,RMVar_hsa_circ_307970,RMVar_hsa_circ_155654,RMVar_hsa_circ_306219,RMVar_hsa_circ_155659,RMVar_hsa_circ_71388,RMVar_hsa_circ_155661,RMVar_hsa_circ_276642,RMVar_hsa_circ_37399,RMVar_hsa_circ_69973,RMVar_hsa_circ_75304,RMVar_hsa_circ_155662,RMVar_hsa_circ_340172,RMVar_hsa_circ_374744,RMVar_hsa_circ_267913,RMVar_hsa_circ_155672,RMVar_hsa_circ_297600,RMVar_hsa_circ_64677,RMVar_hsa_circ_155677,RMVar_hsa_circ_155675,RMVar_hsa_circ_325036,RMVar_hsa_circ_338352,RMVar_hsa_circ_358826,RMVar_hsa_circ_22495,RMVar_hsa_circ_16858,RMVar_hsa_circ_155676,RMVar_hsa_circ_285435,RMVar_hsa_circ_155684,RMVar_hsa_circ_348467,RMVar_hsa_circ_370799,RMVar_hsa_circ_272828,RMVar_hsa_circ_53381,RMVar_hsa_circ_155690,RMVar_hsa_circ_155691,RMVar_hsa_circ_155692,RMVar_hsa_circ_68936,RMVar_hsa_circ_285423,RMVar_hsa_circ_103856,RMVar_hsa_circ_65615,RMVar_hsa_circ_155699,RMVar_hsa_circ_155697,RMVar_hsa_circ_155698,RMVar_hsa_circ_76005,RMVar_hsa_circ_348459,RMVar_hsa_circ_367473,RMVar_hsa_circ_301220,RMVar_hsa_circ_274768,RMVar_hsa_circ_283282,RMVar_hsa_circ_155701,RMVar_hsa_circ_155702,RMVar_hsa_circ_291255,RMVar_hsa_circ_340953,RMVar_hsa_circ_275975,RMVar_hsa_circ_278654,RMVar_hsa_circ_89244,RMVar_hsa_circ_155703,RMVar_hsa_circ_155705,RMVar_hsa_circ_155706,RMVar_hsa_circ_155707,RMVar_hsa_circ_155704 42607 RMVar_ID_42607 Human_SNP_ID_495774092 A-to-I Human chr12 - 31446179 31446179 31446179 GCACCACTGCACTCCCGCCTGGGCAACAGAGCAAGACTCCGTCTCAAAAAAATAAAAAGAAAGCA GCACCACTGCACTCCCGCCTGGGCAACAGAGCGAGACTCCGTCTCAAAAAAATAAAAAGAAAGCA T C DENND5B Ensembl:ENSG00000170456 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1049933390 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113567,RMVar_hsa_circ_307970,RMVar_hsa_circ_155654,RMVar_hsa_circ_306219,RMVar_hsa_circ_155659,RMVar_hsa_circ_71388,RMVar_hsa_circ_155661,RMVar_hsa_circ_276642,RMVar_hsa_circ_37399,RMVar_hsa_circ_69973,RMVar_hsa_circ_75304,RMVar_hsa_circ_155662,RMVar_hsa_circ_340172,RMVar_hsa_circ_374744,RMVar_hsa_circ_267913,RMVar_hsa_circ_155672,RMVar_hsa_circ_297600,RMVar_hsa_circ_64677,RMVar_hsa_circ_155677,RMVar_hsa_circ_155675,RMVar_hsa_circ_325036,RMVar_hsa_circ_338352,RMVar_hsa_circ_358826,RMVar_hsa_circ_22495,RMVar_hsa_circ_16858,RMVar_hsa_circ_155676,RMVar_hsa_circ_285435,RMVar_hsa_circ_155684,RMVar_hsa_circ_348467,RMVar_hsa_circ_370799,RMVar_hsa_circ_272828,RMVar_hsa_circ_53381,RMVar_hsa_circ_155690,RMVar_hsa_circ_155691,RMVar_hsa_circ_155692,RMVar_hsa_circ_68936,RMVar_hsa_circ_285423,RMVar_hsa_circ_103856,RMVar_hsa_circ_65615,RMVar_hsa_circ_155699,RMVar_hsa_circ_155697,RMVar_hsa_circ_155698,RMVar_hsa_circ_76005,RMVar_hsa_circ_348459,RMVar_hsa_circ_367473,RMVar_hsa_circ_301220,RMVar_hsa_circ_274768,RMVar_hsa_circ_283282,RMVar_hsa_circ_155701,RMVar_hsa_circ_155702,RMVar_hsa_circ_291255,RMVar_hsa_circ_340953,RMVar_hsa_circ_275975,RMVar_hsa_circ_278654,RMVar_hsa_circ_89244,RMVar_hsa_circ_155703,RMVar_hsa_circ_155705,RMVar_hsa_circ_155706,RMVar_hsa_circ_155707,RMVar_hsa_circ_155704 42608 RMVar_ID_42608 Human_SNP_ID_495774109 A-to-I Human chr12 - 31446251 31446251 31446251 CCAGCTACTAGGGAGGCTGACATAGAAGAATCACTTGAACCCGGGAGGCGGAGGTTGCAGTGAGC CCAGCTACTAGGGAGGCTGACATAGAAGAATCCCTTGAACCCGGGAGGCGGAGGTTGCAGTGAGC T G DENND5B Ensembl:ENSG00000170456 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1171547878 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11924042 RMVar_hsa_circ_113567,RMVar_hsa_circ_307970,RMVar_hsa_circ_155654,RMVar_hsa_circ_306219,RMVar_hsa_circ_155659,RMVar_hsa_circ_71388,RMVar_hsa_circ_155661,RMVar_hsa_circ_276642,RMVar_hsa_circ_37399,RMVar_hsa_circ_69973,RMVar_hsa_circ_75304,RMVar_hsa_circ_155662,RMVar_hsa_circ_340172,RMVar_hsa_circ_374744,RMVar_hsa_circ_267913,RMVar_hsa_circ_155672,RMVar_hsa_circ_297600,RMVar_hsa_circ_64677,RMVar_hsa_circ_155677,RMVar_hsa_circ_155675,RMVar_hsa_circ_325036,RMVar_hsa_circ_338352,RMVar_hsa_circ_358826,RMVar_hsa_circ_22495,RMVar_hsa_circ_16858,RMVar_hsa_circ_155676,RMVar_hsa_circ_285435,RMVar_hsa_circ_155684,RMVar_hsa_circ_348467,RMVar_hsa_circ_370799,RMVar_hsa_circ_272828,RMVar_hsa_circ_53381,RMVar_hsa_circ_155690,RMVar_hsa_circ_155691,RMVar_hsa_circ_155692,RMVar_hsa_circ_68936,RMVar_hsa_circ_285423,RMVar_hsa_circ_103856,RMVar_hsa_circ_65615,RMVar_hsa_circ_155699,RMVar_hsa_circ_155697,RMVar_hsa_circ_155698,RMVar_hsa_circ_76005,RMVar_hsa_circ_348459,RMVar_hsa_circ_367473,RMVar_hsa_circ_301220,RMVar_hsa_circ_274768,RMVar_hsa_circ_283282,RMVar_hsa_circ_155701,RMVar_hsa_circ_155702,RMVar_hsa_circ_291255,RMVar_hsa_circ_340953,RMVar_hsa_circ_275975,RMVar_hsa_circ_278654,RMVar_hsa_circ_89244,RMVar_hsa_circ_155703,RMVar_hsa_circ_155705,RMVar_hsa_circ_155706,RMVar_hsa_circ_155707,RMVar_hsa_circ_155704 42609 RMVar_ID_42609 Human_SNP_ID_495774232 A-to-I Human chr12 - 31446773 31446773 31446773 ACGCCATTCTCCTGCCCCGAGTAGCTGGGACTATAGGCGCCCACCACCACACCCGGCTAATTTTT ACGCCATTCTCCTGCCCCGAGTAGCTGGGACTGTAGGCGCCCACCACCACACCCGGCTAATTTTT T C DENND5B Ensembl:ENSG00000170456 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs985543650 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113567,RMVar_hsa_circ_307970,RMVar_hsa_circ_155654,RMVar_hsa_circ_306219,RMVar_hsa_circ_155659,RMVar_hsa_circ_71388,RMVar_hsa_circ_155661,RMVar_hsa_circ_276642,RMVar_hsa_circ_37399,RMVar_hsa_circ_69973,RMVar_hsa_circ_75304,RMVar_hsa_circ_155662,RMVar_hsa_circ_340172,RMVar_hsa_circ_374744,RMVar_hsa_circ_267913,RMVar_hsa_circ_155672,RMVar_hsa_circ_297600,RMVar_hsa_circ_64677,RMVar_hsa_circ_155677,RMVar_hsa_circ_155675,RMVar_hsa_circ_325036,RMVar_hsa_circ_338352,RMVar_hsa_circ_358826,RMVar_hsa_circ_22495,RMVar_hsa_circ_16858,RMVar_hsa_circ_155676,RMVar_hsa_circ_285435,RMVar_hsa_circ_155684,RMVar_hsa_circ_348467,RMVar_hsa_circ_370799,RMVar_hsa_circ_272828,RMVar_hsa_circ_53381,RMVar_hsa_circ_155690,RMVar_hsa_circ_155691,RMVar_hsa_circ_155692,RMVar_hsa_circ_68936,RMVar_hsa_circ_285423,RMVar_hsa_circ_103856,RMVar_hsa_circ_65615,RMVar_hsa_circ_155699,RMVar_hsa_circ_155697,RMVar_hsa_circ_155698,RMVar_hsa_circ_76005,RMVar_hsa_circ_348459,RMVar_hsa_circ_367473,RMVar_hsa_circ_301220,RMVar_hsa_circ_274768,RMVar_hsa_circ_283282,RMVar_hsa_circ_155701,RMVar_hsa_circ_155702,RMVar_hsa_circ_291255,RMVar_hsa_circ_340953,RMVar_hsa_circ_275975,RMVar_hsa_circ_278654,RMVar_hsa_circ_89244,RMVar_hsa_circ_155703,RMVar_hsa_circ_155705,RMVar_hsa_circ_155706,RMVar_hsa_circ_155707,RMVar_hsa_circ_155704 42610 RMVar_ID_42610 Human_SNP_ID_495775402 A-to-I Human chr12 - 31450621 31450621 31450621 GCTGGGCATGGTGGCTCACACTTGTAATCCCAACACTAGGAGGTTGAGGCTGGAGGATCATTTGA GCTGGGCATGGTGGCTCACACTTGTAATCCCATCACTAGGAGGTTGAGGCTGGAGGATCATTTGA T A DENND5B Ensembl:ENSG00000170456 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1409520516 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11924088 RMVar_hsa_circ_113567,RMVar_hsa_circ_71388,RMVar_hsa_circ_155661,RMVar_hsa_circ_37399,RMVar_hsa_circ_69973,RMVar_hsa_circ_75304,RMVar_hsa_circ_340172,RMVar_hsa_circ_267913,RMVar_hsa_circ_64677,RMVar_hsa_circ_338352,RMVar_hsa_circ_358826,RMVar_hsa_circ_22495,RMVar_hsa_circ_16858,RMVar_hsa_circ_155676,RMVar_hsa_circ_348467,RMVar_hsa_circ_370799,RMVar_hsa_circ_53381,RMVar_hsa_circ_155691,RMVar_hsa_circ_155692,RMVar_hsa_circ_68936,RMVar_hsa_circ_103856,RMVar_hsa_circ_65615,RMVar_hsa_circ_155699,RMVar_hsa_circ_155698,RMVar_hsa_circ_76005,RMVar_hsa_circ_348459,RMVar_hsa_circ_367473,RMVar_hsa_circ_301220,RMVar_hsa_circ_283282,RMVar_hsa_circ_155702,RMVar_hsa_circ_291255,RMVar_hsa_circ_340953,RMVar_hsa_circ_278654,RMVar_hsa_circ_89244,RMVar_hsa_circ_155708,RMVar_hsa_circ_155705,RMVar_hsa_circ_155706,RMVar_hsa_circ_155707,RMVar_hsa_circ_155704,RMVar_hsa_circ_311804,RMVar_hsa_circ_347030,RMVar_hsa_circ_355601,RMVar_hsa_circ_324301,RMVar_hsa_circ_283539,RMVar_hsa_circ_155710,RMVar_hsa_circ_155711,RMVar_hsa_circ_155709 42611 RMVar_ID_42611 Human_SNP_ID_495775403 A-to-I Human chr12 - 31450621 31450621 31450621 GCTGGGCATGGTGGCTCACACTTGTAATCCCAACACTAGGAGGTTGAGGCTGGAGGATCATTTGA GCTGGGCATGGTGGCTCACACTTGTAATCCCAGCACTAGGAGGTTGAGGCTGGAGGATCATTTGA T C DENND5B Ensembl:ENSG00000170456 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1409520516 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11924088 RMVar_hsa_circ_113567,RMVar_hsa_circ_71388,RMVar_hsa_circ_155661,RMVar_hsa_circ_37399,RMVar_hsa_circ_69973,RMVar_hsa_circ_75304,RMVar_hsa_circ_340172,RMVar_hsa_circ_267913,RMVar_hsa_circ_64677,RMVar_hsa_circ_338352,RMVar_hsa_circ_358826,RMVar_hsa_circ_22495,RMVar_hsa_circ_16858,RMVar_hsa_circ_155676,RMVar_hsa_circ_348467,RMVar_hsa_circ_370799,RMVar_hsa_circ_53381,RMVar_hsa_circ_155691,RMVar_hsa_circ_155692,RMVar_hsa_circ_68936,RMVar_hsa_circ_103856,RMVar_hsa_circ_65615,RMVar_hsa_circ_155699,RMVar_hsa_circ_155698,RMVar_hsa_circ_76005,RMVar_hsa_circ_348459,RMVar_hsa_circ_367473,RMVar_hsa_circ_301220,RMVar_hsa_circ_283282,RMVar_hsa_circ_155702,RMVar_hsa_circ_291255,RMVar_hsa_circ_340953,RMVar_hsa_circ_278654,RMVar_hsa_circ_89244,RMVar_hsa_circ_155708,RMVar_hsa_circ_155705,RMVar_hsa_circ_155706,RMVar_hsa_circ_155707,RMVar_hsa_circ_155704,RMVar_hsa_circ_311804,RMVar_hsa_circ_347030,RMVar_hsa_circ_355601,RMVar_hsa_circ_324301,RMVar_hsa_circ_283539,RMVar_hsa_circ_155710,RMVar_hsa_circ_155711,RMVar_hsa_circ_155709 42612 RMVar_ID_42612 Human_SNP_ID_495776229 A-to-I Human chr12 - 31454090 31454090 31454090 TTGCCCAGGCTGGAGTGCAGTGGCACGATCTTAGCTCACTGCAACCTCTGCCTCCTGAGGTCAAG TTGCCCAGGCTGGAGTGCAGTGGCACGATCTTGGCTCACTGCAACCTCTGCCTCCTGAGGTCAAG T C DENND5B Ensembl:ENSG00000170456 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1358511212 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113567,RMVar_hsa_circ_71388,RMVar_hsa_circ_155661,RMVar_hsa_circ_37399,RMVar_hsa_circ_69973,RMVar_hsa_circ_75304,RMVar_hsa_circ_340172,RMVar_hsa_circ_267913,RMVar_hsa_circ_64677,RMVar_hsa_circ_338352,RMVar_hsa_circ_358826,RMVar_hsa_circ_16858,RMVar_hsa_circ_155676,RMVar_hsa_circ_348467,RMVar_hsa_circ_370799,RMVar_hsa_circ_53381,RMVar_hsa_circ_155691,RMVar_hsa_circ_155692,RMVar_hsa_circ_68936,RMVar_hsa_circ_103856,RMVar_hsa_circ_155699,RMVar_hsa_circ_155698,RMVar_hsa_circ_76005,RMVar_hsa_circ_348459,RMVar_hsa_circ_367473,RMVar_hsa_circ_301220,RMVar_hsa_circ_283282,RMVar_hsa_circ_155702,RMVar_hsa_circ_291255,RMVar_hsa_circ_340953,RMVar_hsa_circ_89244,RMVar_hsa_circ_155708,RMVar_hsa_circ_155705,RMVar_hsa_circ_155706,RMVar_hsa_circ_155707,RMVar_hsa_circ_347030,RMVar_hsa_circ_355601,RMVar_hsa_circ_324301,RMVar_hsa_circ_283539,RMVar_hsa_circ_155710,RMVar_hsa_circ_155709,RMVar_hsa_circ_155715,RMVar_hsa_circ_302573,RMVar_hsa_circ_338144,RMVar_hsa_circ_280522,RMVar_hsa_circ_155714 42613 RMVar_ID_42613 Human_SNP_ID_495790409 A-to-I Human chr12 - 31510974 31510974 31510974 CCCCCGCCTTGACCTCCCAAAATGTTAGGATTACAGGCATGAGCCACCACACCCAGCCCTGAGTA CCCCCGCCTTGACCTCCCAAAATGTTAGGATTGCAGGCATGAGCCACCACACCCAGCCCTGAGTA T C DENND5B Ensembl:ENSG00000170456 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1043419854 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89244,RMVar_hsa_circ_155707 42614 RMVar_ID_42614 Human_SNP_ID_495791750 A-to-I Human chr12 - 31516400 31516400 31516400 TGATCACAGCTCACTGCAACCTCACCATCCCTAGACTCAGGTGATCCAGTTCAACCTCCCAAGTA TGATCACAGCTCACTGCAACCTCACCATCCCTGGACTCAGGTGATCCAGTTCAACCTCCCAAGTA T C DENND5B Ensembl:ENSG00000170456 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978073475 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89244,RMVar_hsa_circ_155707 42615 RMVar_ID_42615 Human_SNP_ID_495793220 A-to-I Human chr12 - 31522536 31522536 31522536 GGAGCCTGAACTGGGGAGGATGGCTTGAGCCCAGGAGGCAGAGGTTGCAGTGAGCTAGATCGTGC GGAGCCTGAACTGGGGAGGATGGCTTGAGCCCCGGAGGCAGAGGTTGCAGTGAGCTAGATCGTGC T G DENND5B Ensembl:ENSG00000170456 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1382726810 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89244,RMVar_hsa_circ_155707 42616 RMVar_ID_42616 Human_SNP_ID_495796219 A-to-I Human chr12 - 31535028 31535028 31535028 GCTCTGTCACCCAGGCTTGGGTGCAGTGGTGCAATCTGCGCTCACTGCAACCTCCACCTCCCAGG GCTCTGTCACCCAGGCTTGGGTGCAGTGGTGCGATCTGCGCTCACTGCAACCTCCACCTCCCAGG T C ANKRD49P2,DENND5B Ensembl:ENSG00000225349,Ensembl:ENSG00000170456 Pseudogene,Protein coding exon,intron GSE100210;GSE107867 HepG2 cell line;ASD brains,cerebellum - 29129909,30559470 RNA-Seq:(High) rs996785923 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8179809,Human_RBP_ID_11924734,Human_RBP_ID_24964205 RMVar_hsa_circ_89244,RMVar_hsa_circ_155707 42617 RMVar_ID_42617 Human_SNP_ID_495798539 A-to-I Human chr12 - 31544566 31544566 31544566 ATTTGATAGTTATTGGCTGGGCATGGTGGTTCACACTTCTAATCCCAACACTTTGGGAGACTGAG ATTTGATAGTTATTGGCTGGGCATGGTGGTTCGCACTTCTAATCCCAACACTTTGGGAGACTGAG T C DENND5B Ensembl:ENSG00000170456 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs568679805 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11924856 RMVar_hsa_circ_89244,RMVar_hsa_circ_155707 42618 RMVar_ID_42618 Human_SNP_ID_495799434 A-to-I Human chr12 - 31548273 31548273 31548273 CCTATACCTCAGCTTTCCGAATAGCTGGGGCTATAGGTATATGCCACCATGTCTGGCTAATTTTT CCTATACCTCAGCTTTCCGAATAGCTGGGGCTGTAGGTATATGCCACCATGTCTGGCTAATTTTT T C DENND5B Ensembl:ENSG00000170456 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs757013991 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6175253 RMVar_hsa_circ_89244,RMVar_hsa_circ_155707 42619 RMVar_ID_42619 Human_SNP_ID_495804572 A-to-I Human chr12 - 31567976 31567976 31567976 AAAGAGGCCAGTTGTGGTGGCTCACATCTGTAATCCCGTACTTTGGAAGGCCGAGGTGGGAGGAT AAAGAGGCCAGTTGTGGTGGCTCACATCTGTAGTCCCGTACTTTGGAAGGCCGAGGTGGGAGGAT T C DENND5B Ensembl:ENSG00000170456 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,temporal_cortex - 29129909,30559470 RNA-Seq:(High) rs1451288002 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11925163 RMVar_hsa_circ_89244,RMVar_hsa_circ_155707 42620 RMVar_ID_42620 Human_SNP_ID_495807968 A-to-I Human chr12 - 31580770 31580770 31580770 CTAAAATGGACCAGGCGCGGTGGCTTAGCCCTATAATCCCAGCACTTTGGGTGGCCGAGACGGGT CTAAAATGGACCAGGCGCGGTGGCTTAGCCCTGTAATCCCAGCACTTTGGGTGGCCGAGACGGGT T C DENND5B Ensembl:ENSG00000170456 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs369939541 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11925491 RMVar_hsa_circ_89244,RMVar_hsa_circ_155707 42621 RMVar_ID_42621 Human_SNP_ID_495808264 A-to-I Human chr12 - 31581946 31581946 31581946 ATTTACATGGAATTTGCATCGTACTGAGTATTATAACTAACCAGGAGGTGACTTAAAGTGTACGG ATTTACATGGAATTTGCATCGTACTGAGTATTGTAACTAACCAGGAGGTGACTTAAAGTGTACGG T C DENND5B Ensembl:ENSG00000170456 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054071766 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11925512 RMVar_hsa_circ_89244,RMVar_hsa_circ_155707 42622 RMVar_ID_42622 Human_SNP_ID_495834262 A-to-I Human chr12 - 31684635 31684635 31684635 AACCCTGTCCGTACTAAAAATACAAAAAAATTAGCCGGGCATGGTGGCGGGCGCCTGTAGTCCCA AACCCTGTCCGTACTAAAAATACAAAAAAATTGGCCGGGCATGGTGGCGGGCGCCTGTAGTCCCA T C AMN1 Ensembl:ENSG00000151743 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991167587 Functional Loss SNV dbSNP153 33..33 33 - - - 42623 RMVar_ID_42623 Human_SNP_ID_495835171 A-to-I Human chr12 - 31688557 31688557 31688557 GCAATCCGCCTGCCTTGGCCTCCCAAAGTGCTAGGATTACAGACGTTAGCTGCCGCGCCCGGCCT GCAATCCGCCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGACGTTAGCTGCCGCGCCCGGCCT T C AMN1 Ensembl:ENSG00000151743 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904916669 Functional Loss SNV dbSNP153 33..33 33 - - - 42624 RMVar_ID_42624 Human_SNP_ID_495839806 A-to-I Human chr12 - 31709056 31709056 31709056 ATCCCTCTTCAGCCTCCTGAGTAGTTGGGACTATAGGTGTACACCACCATGCCTGGCTAATTTTT ATCCCTCTTCAGCCTCCTGAGTAGTTGGGACTGTAGGTGTACACCACCATGCCTGGCTAATTTTT T C AMN1 Ensembl:ENSG00000151743 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs777650355 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1352925 RMVar_hsa_circ_275166,RMVar_hsa_circ_304449,RMVar_hsa_circ_100276,RMVar_hsa_circ_67265,RMVar_hsa_circ_155723,RMVar_hsa_circ_155724,RMVar_hsa_circ_309409,RMVar_hsa_circ_155729,RMVar_hsa_circ_278078,RMVar_hsa_circ_155731,RMVar_hsa_circ_155732 42625 RMVar_ID_42625 Human_SNP_ID_495839829 A-to-I Human chr12 - 31709128 31709128 31709128 CTCCGTTGCCCAGGCTGGAGTACAGTGGTGCAATCTCAGCTCACTGCAACCTCCGCTGCCTGGAC CTCCGTTGCCCAGGCTGGAGTACAGTGGTGCAGTCTCAGCTCACTGCAACCTCCGCTGCCTGGAC T C AMN1 Ensembl:ENSG00000151743 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1193557383 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1352906,Human_Splice_Rec_1352907,Human_Splice_Rec_1352916,Human_Splice_Rec_1352917,Human_Splice_Rec_1352924,Human_Splice_Rec_1352925,Human_Splice_Rec_1352930,Human_Splice_Rec_1352938 RMVar_hsa_circ_275166,RMVar_hsa_circ_304449,RMVar_hsa_circ_100276,RMVar_hsa_circ_67265,RMVar_hsa_circ_155723,RMVar_hsa_circ_155724,RMVar_hsa_circ_309409,RMVar_hsa_circ_155729,RMVar_hsa_circ_278078,RMVar_hsa_circ_155731,RMVar_hsa_circ_155732 42626 RMVar_ID_42626 Human_SNP_ID_495839830 A-to-I Human chr12 - 31709129 31709129 31709129 GCTCCGTTGCCCAGGCTGGAGTACAGTGGTGCAATCTCAGCTCACTGCAACCTCCGCTGCCTGGA GCTCCGTTGCCCAGGCTGGAGTACAGTGGTGCCATCTCAGCTCACTGCAACCTCCGCTGCCTGGA T G AMN1 Ensembl:ENSG00000151743 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1261741010 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1352906,Human_Splice_Rec_1352907,Human_Splice_Rec_1352916,Human_Splice_Rec_1352917,Human_Splice_Rec_1352924,Human_Splice_Rec_1352925,Human_Splice_Rec_1352930,Human_Splice_Rec_1352938 RMVar_hsa_circ_275166,RMVar_hsa_circ_304449,RMVar_hsa_circ_100276,RMVar_hsa_circ_67265,RMVar_hsa_circ_155723,RMVar_hsa_circ_155724,RMVar_hsa_circ_309409,RMVar_hsa_circ_155729,RMVar_hsa_circ_278078,RMVar_hsa_circ_155731,RMVar_hsa_circ_155732 42627 RMVar_ID_42627 Human_SNP_ID_495839835 A-to-I Human chr12 - 31709139 31709139 31709139 ACAGGGTCATGCTCCGTTGCCCAGGCTGGAGTACAGTGGTGCAATCTCAGCTCACTGCAACCTCC ACAGGGTCATGCTCCGTTGCCCAGGCTGGAGTGCAGTGGTGCAATCTCAGCTCACTGCAACCTCC T C AMN1 Ensembl:ENSG00000151743 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1431067095 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1352906,Human_Splice_Rec_1352907,Human_Splice_Rec_1352916,Human_Splice_Rec_1352917,Human_Splice_Rec_1352924,Human_Splice_Rec_1352925,Human_Splice_Rec_1352930,Human_Splice_Rec_1352938 RMVar_hsa_circ_275166,RMVar_hsa_circ_304449,RMVar_hsa_circ_100276,RMVar_hsa_circ_67265,RMVar_hsa_circ_155723,RMVar_hsa_circ_155724,RMVar_hsa_circ_309409,RMVar_hsa_circ_155729,RMVar_hsa_circ_278078,RMVar_hsa_circ_155731,RMVar_hsa_circ_155732 42628 RMVar_ID_42628 Human_SNP_ID_495862084 A-to-I Human chr12 - 31800226 31800226 31800226 CTGTGGCTCACATCTGTAATTCCAGCAATTTGAGAGGCCGAGGCAGGCAGAACACTTGAGGCCAG CTGTGGCTCACATCTGTAATTCCAGCAATTTGGGAGGCCGAGGCAGGCAGAACACTTGAGGCCAG T C LINC02422 RNACentral:URS0000D5A1EA lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1400561846 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102566,RMVar_hsa_circ_155733 42629 RMVar_ID_42629 Human_SNP_ID_495906802 A-to-I Human chr12 + 31972129 31972129 31972129 GCTGTGCCCCTTCTCATGTGACCTTGCCTTCTACATCTCTTGAACTGAATCCTTGGTAATATACT GCTGTGCCCCTTCTCATGTGACCTTGCCTTCTGCATCTCTTGAACTGAATCCTTGGTAATATACT A G RESF1 Ensembl:ENSG00000174718 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348471786 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_155734,RMVar_hsa_circ_333794 42630 RMVar_ID_42630 Human_SNP_ID_495907342 A-to-I Human chr12 + 31973949 31973949 31973949 CTTCAGATCCCACAGGTTGAGGACTCAGTCCCACAAGACTGCCCCTGACTTCGCCAGACCTGTAC CTTCAGATCCCACAGGTTGAGGACTCAGTCCCGCAAGACTGCCCCTGACTTCGCCAGACCTGTAC A G RESF1 Ensembl:ENSG00000174718 Protein coding intron GSE107867 ASD brains,frontal_cortex;ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1038537304 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_333794 42631 RMVar_ID_42631 Human_SNP_ID_495912279 A-to-I Human chr12 + 31988933 31988933 31988933 CCAGGCTGGTCTCAAACTCCTGAACTCAGGTGATCCACCTGCCTCGGCCTCCCAAAATGCTGGGA CCAGGCTGGTCTCAAACTCCTGAACTCAGGTGTTCCACCTGCCTCGGCCTCCCAAAATGCTGGGA A T RESF1 Ensembl:ENSG00000174718 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1344714144 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122190,RMVar_hsa_circ_155737 42632 RMVar_ID_42632 Human_SNP_ID_495912333 A-to-I Human chr12 + 31989141 31989141 31989141 AGAGGGGGCTGGGCACGGTGGCTCACACCTGTAATCTCAGCACTTTGGGAGGCCGAGGCAGGCGG AGAGGGGGCTGGGCACGGTGGCTCACACCTGTGATCTCAGCACTTTGGGAGGCCGAGGCAGGCGG A G RESF1 Ensembl:ENSG00000174718 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs980956673 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122190,RMVar_hsa_circ_155737 42633 RMVar_ID_42633 Human_SNP_ID_495912367 A-to-I Human chr12 + 31989245 31989245 31989245 GGTGAAACCCTGTCTCTACTGAAAATATAAAAAATAAGCCGAGTGTGGTGGCGGGCACCTGTAGT GGTGAAACCCTGTCTCTACTGAAAATATAAAACATAAGCCGAGTGTGGTGGCGGGCACCTGTAGT A C RESF1 Ensembl:ENSG00000174718 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1263586965 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122190,RMVar_hsa_circ_155737 42634 RMVar_ID_42634 Human_SNP_ID_495912514 A-to-I Human chr12 + 31989715 31989715 31989715 GCCTACTAAAAATATAAAAATTAGTCAGGTGTAGTGGCACATGCCTGTAATACCAGCTATTCAGT GCCTACTAAAAATATAAAAATTAGTCAGGTGTCGTGGCACATGCCTGTAATACCAGCTATTCAGT A C RESF1 Ensembl:ENSG00000174718 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1426907320 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18625215 RMVar_hsa_circ_122190,RMVar_hsa_circ_155737 42635 RMVar_ID_42635 Human_SNP_ID_495913885 A-to-I Human chr12 + 31994209 31994209 31994209 CCCCAGCTTCCCAAAGTGCTGGGATTACAAGCATGAGCTACTGGGTCCAGCCTGTTTGTTTTTTT CCCCAGCTTCCCAAAGTGCTGGGATTACAAGCTTGAGCTACTGGGTCCAGCCTGTTTGTTTTTTT A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956419521 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_155739,RMVar_hsa_circ_155740 42636 RMVar_ID_42636 Human_SNP_ID_495915504 A-to-I Human chr12 + 31999727 31999727 31999727 TTTTGTATTTTGGGAGTTTTTTTGTAGATAATAGGGTTTCGCCATGTTGCCCAGGATGGTGAACT TTTTGTATTTTGGGAGTTTTTTTGTAGATAATGGGGTTTCGCCATGTTGCCCAGGATGGTGAACT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1346792539 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_155739 42637 RMVar_ID_42637 Human_SNP_ID_495948197 A-to-I Human chr12 + 32119629 32119629 32119629 TGCAGTGGCTCATGCCTGTAATGCCAGCACTTAGGGAGACCAAGGCAGATGGATCATATGAGGCC TGCAGTGGCTCATGCCTGTAATGCCAGCACTTGGGGAGACCAAGGCAGATGGATCATATGAGGCC A G BICD1 Ensembl:ENSG00000151746 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1326106498 Functional Loss SNV dbSNP153 33..33 33 - - - 42638 RMVar_ID_42638 Human_SNP_ID_495948839 A-to-I Human chr12 + 32122005 32122005 32122005 CCAGCTAATTTTTTTGTATTTTTTGTAGAGACAGTGTCTCACAATGTTGTGCAGGCTCGTCTCAA CCAGCTAATTTTTTTGTATTTTTTGTAGAGACTGTGTCTCACAATGTTGTGCAGGCTCGTCTCAA A T BICD1 Ensembl:ENSG00000151746 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1035878005 Functional Loss SNV dbSNP153 33..33 33 - - - 42639 RMVar_ID_42639 Human_SNP_ID_495951197 A-to-I Human chr12 + 32132162 32132162 32132162 GATGGGGGCTGGGCACTGTGGCTCACACCTGTAATCCCAGCTGTTTGGGAGGCCAAGGTGGGCAG GATGGGGGCTGGGCACTGTGGCTCACACCTGTCATCCCAGCTGTTTGGGAGGCCAAGGTGGGCAG A C BICD1 Ensembl:ENSG00000151746 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1339931489 Functional Loss SNV dbSNP153 33..33 33 - - - 42640 RMVar_ID_42640 Human_SNP_ID_495972438 A-to-I Human chr12 + 32223371 32223371 32223371 GAAACCCCGTCTCTACTAAAAATACAAAAATTAGCTGGGCATGGTGGCGAATGCCCGTAGTCCCA GAAACCCCGTCTCTACTAAAAATACAAAAATTGGCTGGGCATGGTGGCGAATGCCCGTAGTCCCA A G BICD1 Ensembl:ENSG00000151746 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1003796211 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100488,RMVar_hsa_circ_155741,RMVar_hsa_circ_64326 42641 RMVar_ID_42641 Human_SNP_ID_495980961 A-to-I Human chr12 + 32256152 32256152 32256152 ATAGCTCACTGCAACCTTGACCCCCTGGGCTCAAGCAATCCTCCTGTCTCAGCCTCCTGAGTAGG ATAGCTCACTGCAACCTTGACCCCCTGGGCTCCAGCAATCCTCCTGTCTCAGCCTCCTGAGTAGG A C BICD1 Ensembl:ENSG00000151746 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs368093084 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100488,RMVar_hsa_circ_155741,RMVar_hsa_circ_64326 42642 RMVar_ID_42642 Human_SNP_ID_496001898 A-to-I Human chr12 + 32346012 32346012 32346012 CTCTACAAAAAATAAAAAGATTATTCGGGCATAGTGGCATGCGCCTGTACTCTCAGCTACTCAGG CTCTACAAAAAATAAAAAGATTATTCGGGCATGGTGGCATGCGCCTGTACTCTCAGCTACTCAGG A G BICD1 Ensembl:ENSG00000151746 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1420214318 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1166490 42643 RMVar_ID_42643 Human_SNP_ID_496002449 A-to-I Human chr12 + 32347045 32347045 32347045 ACAATATTGCCTCACCGCAACCTCCGCCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCA ACAATATTGCCTCACCGCAACCTCCGCCTCCCCGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCA A C BICD1 Ensembl:ENSG00000151746 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs890787312 Functional Loss SNV dbSNP153 33..33 33 - - - 42644 RMVar_ID_42644 Human_SNP_ID_496002450 A-to-I Human chr12 + 32347051 32347051 32347051 TTGCCTCACCGCAACCTCCGCCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAACTAGC TTGCCTCACCGCAACCTCCGCCTCCCAGGTTCGAGCGATTCTCCTGCCTCAGCCTCCCAACTAGC A G BICD1 Ensembl:ENSG00000151746 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917473852 Functional Loss SNV dbSNP153 33..33 33 - - - 42645 RMVar_ID_42645 Human_SNP_ID_496030281 A-to-I Human chr12 + 32460394 32460394 32460394 ATAATTAGCCACTGGTGGTGGTGCGTGCCCGTAGCACCAGCTACTTGGGAGGCTGATGCTTGAGG ATAATTAGCCACTGGTGGTGGTGCGTGCCCGTGGCACCAGCTACTTGGGAGGCTGATGCTTGAGG A G FGD4 Ensembl:ENSG00000139132 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs999991681 Functional Loss SNV dbSNP153 33..33 33 - - - 42646 RMVar_ID_42646 Human_SNP_ID_496037032 A-to-I Human chr12 + 32487627 32487627 32487627 TTTTGTGTTTTTAGTAGAGACGAGGTTTTGCCATGTTGGCCAGGCTGGTCTTGAACTCCGGACCT TTTTGTGTTTTTAGTAGAGACGAGGTTTTGCCGTGTTGGCCAGGCTGGTCTTGAACTCCGGACCT A G FGD4 Ensembl:ENSG00000139132 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1046128023 Functional Loss SNV dbSNP153 33..33 33 - - - 42647 RMVar_ID_42647 Human_SNP_ID_496063874 A-to-I Human chr12 + 32599808 32599808 32599808 CTGACCTTGTGATCCTCCCACCTTGGCCTCTCAAAGTGCTGGGATTACAGGCGTGAGCCACCACG CTGACCTTGTGATCCTCCCACCTTGGCCTCTCGAAGTGCTGGGATTACAGGCGTGAGCCACCACG A G FGD4 Ensembl:ENSG00000139132 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1248309869 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2430,RMVar_hsa_circ_31120,RMVar_hsa_circ_284213,RMVar_hsa_circ_24938,RMVar_hsa_circ_330758,RMVar_hsa_circ_67525,RMVar_hsa_circ_40384,RMVar_hsa_circ_155753,RMVar_hsa_circ_155751,RMVar_hsa_circ_155752,RMVar_hsa_circ_294343,RMVar_hsa_circ_328859,RMVar_hsa_circ_330509,RMVar_hsa_circ_325257,RMVar_hsa_circ_289304,RMVar_hsa_circ_56156,RMVar_hsa_circ_274401,RMVar_hsa_circ_36424,RMVar_hsa_circ_155755,RMVar_hsa_circ_155756,RMVar_hsa_circ_155757,RMVar_hsa_circ_155754,RMVar_hsa_circ_155762,RMVar_hsa_circ_155766,RMVar_hsa_circ_286858,RMVar_hsa_circ_332118,RMVar_hsa_circ_155758,RMVar_hsa_circ_79770,RMVar_hsa_circ_333256,RMVar_hsa_circ_333735,RMVar_hsa_circ_291515,RMVar_hsa_circ_300526,RMVar_hsa_circ_290892,RMVar_hsa_circ_120452,RMVar_hsa_circ_280205,RMVar_hsa_circ_103820,RMVar_hsa_circ_155767,RMVar_hsa_circ_155764,RMVar_hsa_circ_155765,RMVar_hsa_circ_155763,RMVar_hsa_circ_155760,RMVar_hsa_circ_155761,RMVar_hsa_circ_155759 42648 RMVar_ID_42648 Human_SNP_ID_496086833 A-to-I Human chr12 + 32689297 32689297 32689297 CTGGCTGACTGCAACTTCTGCCTCCTGAGTTCAAGTGATTCTACTGTCTCAGCTTCCCGAGTAGC CTGGCTGACTGCAACTTCTGCCTCCTGAGTTCGAGTGATTCTACTGTCTCAGCTTCCCGAGTAGC A G DNM1L Ensembl:ENSG00000087470 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1286114187 Functional Loss SNV dbSNP153 33..33 33 - - - 42649 RMVar_ID_42649 Human_SNP_ID_496086852 A-to-I Human chr12 + 32689386 32689386 32689386 CGCCTGGCTAATTTTGTATTTTTAGTAGAGACAAGGTTTCTCCATGTTAGTCAGTCTGGTCTCAA CGCCTGGCTAATTTTGTATTTTTAGTAGAGACGAGGTTTCTCCATGTTAGTCAGTCTGGTCTCAA A G DNM1L Ensembl:ENSG00000087470 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs892906775 Functional Loss SNV dbSNP153 33..33 33 - - - 42650 RMVar_ID_42650 Human_SNP_ID_496089347 A-to-I Human chr12 + 32700223 32700223 32700223 CTTACTGCAACCTCCACCTCCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGG CTTACTGCAACCTCCACCTCCCGGGTTCAAGCCATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGG A C DNM1L Ensembl:ENSG00000087470 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs7968325 Functional Loss SNV dbSNP153 33..33 33 - - - 42651 RMVar_ID_42651 Human_SNP_ID_496089348 A-to-I Human chr12 + 32700223 32700223 32700223 CTTACTGCAACCTCCACCTCCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGG CTTACTGCAACCTCCACCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGG A G DNM1L Ensembl:ENSG00000087470 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs7968325 Functional Loss SNV dbSNP153 33..33 33 - - - 42652 RMVar_ID_42652 Human_SNP_ID_496092803 A-to-I Human chr12 + 32714733 32714733 32714733 GTAGACTGGGCTCAGTGGCTCATGCCCGTAATACCAAGCACTTTGGGAGGCCAAGGTGGGTGGAT GTAGACTGGGCTCAGTGGCTCATGCCCGTAATGCCAAGCACTTTGGGAGGCCAAGGTGGGTGGAT A G DNM1L Ensembl:ENSG00000087470 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1264144716 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13641,RMVar_hsa_circ_16255,RMVar_hsa_circ_9583,RMVar_hsa_circ_155786,RMVar_hsa_circ_46523,RMVar_hsa_circ_318657,RMVar_hsa_circ_310722,RMVar_hsa_circ_273934,RMVar_hsa_circ_155790,RMVar_hsa_circ_155791,RMVar_hsa_circ_155789,RMVar_hsa_circ_155794,RMVar_hsa_circ_304245,RMVar_hsa_circ_307360,RMVar_hsa_circ_346354,RMVar_hsa_circ_155793,RMVar_hsa_circ_155795,RMVar_hsa_circ_265798,RMVar_hsa_circ_301961,RMVar_hsa_circ_302351,RMVar_hsa_circ_155796 42653 RMVar_ID_42653 Human_SNP_ID_496095696 A-to-I Human chr12 + 32724482 32724482 32724482 CCTGTAATCCCAGCTACTTAGGAGGCTGAGGCAGGAGAATCGCTTGAACCCAGGTGGTGGAGGTT CCTGTAATCCCAGCTACTTAGGAGGCTGAGGCGGGAGAATCGCTTGAACCCAGGTGGTGGAGGTT A G DNM1L Ensembl:ENSG00000087470 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1291586087 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13641,RMVar_hsa_circ_16255,RMVar_hsa_circ_46523,RMVar_hsa_circ_318657,RMVar_hsa_circ_155791,RMVar_hsa_circ_346354,RMVar_hsa_circ_265798,RMVar_hsa_circ_14700,RMVar_hsa_circ_295101,RMVar_hsa_circ_312853,RMVar_hsa_circ_377894,RMVar_hsa_circ_155798,RMVar_hsa_circ_155799 42654 RMVar_ID_42654 Human_SNP_ID_496095701 A-to-I Human chr12 + 32724501 32724499 32724530 AGGAGGCTGAGGCAGGAGAATCGCTTGAACCCAGGTGGTGGAGGTTGCAGTGAGCTGAGATCGCA AGGAGGCTGAGGCAGGAGAATCGCTTGAACTCAGGTGGTGGAGGTTGCAGTGAGCTGAGATTGCA CCAGGTGGTGGAGGTTGCAGTGAGCTGAGATC TCAGGTGGTGGAGGTTGCAGTGAGCTGAGATT DNM1L Ensembl:ENSG00000087470 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs386761899 Functional Loss MNV dbSNP153 31..62 33 - - - RMVar_hsa_circ_13641,RMVar_hsa_circ_16255,RMVar_hsa_circ_46523,RMVar_hsa_circ_318657,RMVar_hsa_circ_155791,RMVar_hsa_circ_346354,RMVar_hsa_circ_265798,RMVar_hsa_circ_14700,RMVar_hsa_circ_295101,RMVar_hsa_circ_312853,RMVar_hsa_circ_377894,RMVar_hsa_circ_155798,RMVar_hsa_circ_155799 42655 RMVar_ID_42655 Human_SNP_ID_496095702 A-to-I Human chr12 + 32724501 32724501 32724501 AGGAGGCTGAGGCAGGAGAATCGCTTGAACCCAGGTGGTGGAGGTTGCAGTGAGCTGAGATCGCA AGGAGGCTGAGGCAGGAGAATCGCTTGAACCCTGGTGGTGGAGGTTGCAGTGAGCTGAGATCGCA A T DNM1L Ensembl:ENSG00000087470 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1215286735 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13641,RMVar_hsa_circ_16255,RMVar_hsa_circ_46523,RMVar_hsa_circ_318657,RMVar_hsa_circ_155791,RMVar_hsa_circ_346354,RMVar_hsa_circ_265798,RMVar_hsa_circ_14700,RMVar_hsa_circ_295101,RMVar_hsa_circ_312853,RMVar_hsa_circ_377894,RMVar_hsa_circ_155798,RMVar_hsa_circ_155799 42656 RMVar_ID_42656 Human_SNP_ID_496100715 A-to-I Human chr12 + 32744561 32744561 32744561 CATGGAGAAACCCCGTCTCTACTAAAAATACAAAATTGGCCGGGCGTGGTGGCGCATGCCTGTAA CATGGAGAAACCCCGTCTCTACTAAAAATACAGAATTGGCCGGGCGTGGTGGCGCATGCCTGTAA A G DNM1L Ensembl:ENSG00000087470 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1311164005 Functional Loss SNV dbSNP153 33..33 33 - - - 42657 RMVar_ID_42657 Human_SNP_ID_496130709 A-to-I Human chr12 - 32867314 32867314 32867314 TGCTTTCTTTCTATGTTTTGAGACAGGGTCTCACTGTGTCGCTTAGGCTGGAGAGCAGTGGTGTG TGCTTTCTTTCTATGTTTTGAGACAGGGTCTCGCTGTGTCGCTTAGGCTGGAGAGCAGTGGTGTG T C PKP2 Ensembl:ENSG00000057294 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs770838965 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103623,RMVar_hsa_circ_315954,RMVar_hsa_circ_155808,RMVar_hsa_circ_155809 42658 RMVar_ID_42658 Human_SNP_ID_496420501 A-to-I Human chr12 + 34032802 34032802 34032802 GGTCTTGAACACCTGCCTCAAGTGATCCTCCCACCTTGGCCTACCAAAGTGCTGGGATTTACCAT GGTCTTGAACACCTGCCTCAAGTGATCCTCCCGCCTTGGCCTACCAAAGTGCTGGGATTTACCAT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1470694829 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23556951 42659 RMVar_ID_42659 Human_SNP_ID_497813808 A-to-I Human chr12 + 38321584 38321584 38321584 AATTTATTCTCTTCAGAGAGAACTATTAGGTTAGTGCAAAAGTAATTGTGGTTTTTGCCATTGAA AATTTATTCTCTTCAGAGAGAACTATTAGGTTGGTGCAAAAGTAATTGTGGTTTTTGCCATTGAA A G ALG10B Ensembl:ENSG00000175548 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1182908187 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97296,RMVar_hsa_circ_103361,RMVar_hsa_circ_155815,RMVar_hsa_circ_155816 42660 RMVar_ID_42660 Human_SNP_ID_497947467 A-to-I Human chr12 - 38811756 38811756 38811756 CAGATCTTCCTGCCTCAGCCTCCCAAATAGCTAGGACTACAGGTGTGCACCACCACACCCAGCTA CAGATCTTCCTGCCTCAGCCTCCCAAATAGCTGGGACTACAGGTGTGCACCACCACACCCAGCTA T C CPNE8 Ensembl:ENSG00000139117 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569346190 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108827,RMVar_hsa_circ_155822,RMVar_hsa_circ_11593,RMVar_hsa_circ_39635,RMVar_hsa_circ_92273,RMVar_hsa_circ_155828,RMVar_hsa_circ_55755 42661 RMVar_ID_42661 Human_SNP_ID_498074811 A-to-I Human chr12 + 39317846 39317846 39317846 GTAAAAGAAAAGGCAAGACAAGTGCTGAAGGCATACCAATACAAATCTACAACAGGGAATAATGT GTAAAAGAAAAGGCAAGACAAGTGCTGAAGGCGTACCAATACAAATCTACAACAGGGAATAATGT A G lnc-C12orf40-3 RNACentral:URS00009B8BAE lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs948244531 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_155838 42662 RMVar_ID_42662 Human_SNP_ID_498101314 A-to-I Human chr12 - 39432799 39432799 39432799 TGAGACCAGCCCGGCCAGCATGGTGAAACCCTATCTCTACTGAAAATACAAAAATCAGCTGAGCA TGAGACCAGCCCGGCCAGCATGGTGAAACCCTGTCTCTACTGAAAATACAAAAATCAGCTGAGCA T C KIF21A Ensembl:ENSG00000139116 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs544627326 Functional Loss SNV dbSNP153 33..33 33 - - - 42663 RMVar_ID_42663 Human_SNP_ID_498101315 A-to-I Human chr12 - 39432799 39432799 39432799 TGAGACCAGCCCGGCCAGCATGGTGAAACCCTATCTCTACTGAAAATACAAAAATCAGCTGAGCA TGAGACCAGCCCGGCCAGCATGGTGAAACCCTCTCTCTACTGAAAATACAAAAATCAGCTGAGCA T G KIF21A Ensembl:ENSG00000139116 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs544627326 Functional Loss SNV dbSNP153 33..33 33 - - - 42664 RMVar_ID_42664 Human_SNP_ID_498101325 A-to-I Human chr12 - 39432835 39432835 39432835 AGGCTGAGGTGGGCAGATCACTTGAGGTCAGAAGTCTGAGACCAGCCCGGCCAGCATGGTGAAAC AGGCTGAGGTGGGCAGATCACTTGAGGTCAGACGTCTGAGACCAGCCCGGCCAGCATGGTGAAAC T G KIF21A Ensembl:ENSG00000139116 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1235140196 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11930500 42665 RMVar_ID_42665 Human_SNP_ID_22518296 A-to-I Human chr1 + 90032208 90032206 90032209 CCTCTAATTCCCAGAGGTCTGTTGTGAATTCTAATGCTTTCAGAAAATATTACGGAGAATCCCAC CCTCTAATTCCCAGAGGTCTGTTGTGAATTC___TGCTTTCAGAAAATATTACGGAGAATCCCAC CTAA C ZNF326 Ensembl:ENSG00000162664 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1408612895 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_8168106,Human_RBP_ID_11144120 42666 RMVar_ID_42666 Human_SNP_ID_22518298 A-to-I Human chr1 + 90032208 90032208 90032208 CCTCTAATTCCCAGAGGTCTGTTGTGAATTCTAATGCTTTCAGAAAATATTACGGAGAATCCCAC CCTCTAATTCCCAGAGGTCTGTTGTGAATTCTCATGCTTTCAGAAAATATTACGGAGAATCCCAC A C ZNF326 Ensembl:ENSG00000162664 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs556332040 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8168106,Human_RBP_ID_11144120 42667 RMVar_ID_42667 Human_SNP_ID_22518299 A-to-I Human chr1 + 90032208 90032208 90032208 CCTCTAATTCCCAGAGGTCTGTTGTGAATTCTAATGCTTTCAGAAAATATTACGGAGAATCCCAC CCTCTAATTCCCAGAGGTCTGTTGTGAATTCTGATGCTTTCAGAAAATATTACGGAGAATCCCAC A G ZNF326 Ensembl:ENSG00000162664 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs556332040 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8168106,Human_RBP_ID_11144120 42668 RMVar_ID_42668 Human_SNP_ID_22694739 A-to-I Human chr1 - 90792613 90792610 90792614 TCTGTGGCAACTGTGTAATTCATGAATGAATGAATAATAAACAATAAGTCTAACTTGAGGACTTC TCTGTGGCAACTGTGTAATTCATGAATGAAT____AATAAACAATAAGTCTAACTTGAGGACTTC TATTC T LINC02609 Ensembl:ENSG00000233593 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs529651586 Functional Loss DEL dbSNP153 32..35 33 - - - 42669 RMVar_ID_42669 Human_SNP_ID_22694740 A-to-I Human chr1 - 90792610 90792610 90792610 GTGGCAACTGTGTAATTCATGAATGAATGAATAATAAACAATAAGTCTAACTTGAGGACTTCACT GTGGCAACTGTGTAATTCATGAATGAATGAATGATAAACAATAAGTCTAACTTGAGGACTTCACT T C LINC02609 Ensembl:ENSG00000233593 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs755080243 Functional Loss SNV dbSNP153 33..33 33 - - - 42670 RMVar_ID_42670 Human_SNP_ID_22723095 A-to-I Human chr1 - 90914496 90914496 90914496 TTTTGTATTTTTCGTAGAGACAGAGTTTTACCATGTTGCCCAGGCTGTGCTTGAACTCCTGGGCT TTTTGTATTTTTCGTAGAGACAGAGTTTTACCGTGTTGCCCAGGCTGTGCTTGAACTCCTGGGCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1485764489 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_134435 42671 RMVar_ID_42671 Human_SNP_ID_22736539 A-to-I Human chr1 - 90970843 90970843 90970843 GGCATGTGCCACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGG GGCATGTGCCACCACGCCCAGCTAATTTTTGTGTTTTTAGTAGAGACAGGGTTTCACCATGTTGG T C ZNF644 Ensembl:ENSG00000122482 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1005149816 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_134438,RMVar_hsa_circ_266910,RMVar_hsa_circ_353169,RMVar_hsa_circ_134437,RMVar_hsa_circ_134444,RMVar_hsa_circ_134447,RMVar_hsa_circ_281136,RMVar_hsa_circ_304610 42672 RMVar_ID_42672 Human_SNP_ID_22737384 A-to-I Human chr1 - 90974218 90974218 90974218 TTCAAATGATTCTCATGCCTCAGCCTGGGATTACTGGCGCCCACCACCTTGCCCAGCTAATTTTT TTCAAATGATTCTCATGCCTCAGCCTGGGATTCCTGGCGCCCACCACCTTGCCCAGCTAATTTTT T G ZNF644 Ensembl:ENSG00000122482 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1422359621 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23419728 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 42673 RMVar_ID_42673 Human_SNP_ID_22746796 A-to-I Human chr1 - 91012426 91012426 91012426 TCACCCTAGCTGGAGTGCATTGGCGCAATCTCAGCTCACTGCAGCCTTCACCTCCCAGGCTCAAG TCACCCTAGCTGGAGTGCATTGGCGCAATCTCGGCTCACTGCAGCCTTCACCTCCCAGGCTCAAG T C ZNF644 Ensembl:ENSG00000122482 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1425063490 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19427977,Human_RBP_ID_24737815 42674 RMVar_ID_42674 Human_SNP_ID_22746966 A-to-I Human chr1 - 91013141 91013141 91013141 TAAACATGAGAGGCGGAGGTTGCAGTAAGCCAAGATCATGCCACTGCATCCCCACCTGGGCGACA TAAACATGAGAGGCGGAGGTTGCAGTAAGCCAGGATCATGCCACTGCATCCCCACCTGGGCGACA T C ZNF644 Ensembl:ENSG00000122482 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1418468522 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11148048 42675 RMVar_ID_42675 Human_SNP_ID_22869518 A-to-I Human chr1 + 91506852 91506852 91506852 CGTGCCTGTAATTCCAGCTGCCCATGAGGCTGAGGCATGAGAATCTCTTGAACGCAGGAGGCAGA CGTGCCTGTAATTCCAGCTGCCCATGAGGCTGGGGCATGAGAATCTCTTGAACGCAGGAGGCAGA A G CDC7 Ensembl:ENSG00000097046 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1052996274 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11148846 RMVar_hsa_circ_29576,RMVar_hsa_circ_320166,RMVar_hsa_circ_354657,RMVar_hsa_circ_124336,RMVar_hsa_circ_134474,RMVar_hsa_circ_134473 42676 RMVar_ID_42676 Human_SNP_ID_22901389 A-to-I Human chr1 + 91642661 91642661 91642661 TCAAAGACTAAAAAAGTTGAAAACACTGTCTGAGACTGGGAACTTATGAATGATATCAAACCAGT TCAAAGACTAAAAAAGTTGAAAACACTGTCTGGGACTGGGAACTTATGAATGATATCAAACCAGT A G HSP90B3P Ensembl:ENSG00000203914 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879023619 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17456676 42677 RMVar_ID_42677 Human_SNP_ID_22901525 A-to-I Human chr1 - 91642971 91642971 91642971 TCATCTGAGTCCACCACACCCTTGACAAAATTAAGGTACTTAGGCATCATATCATGGAATTCATC TCATCTGAGTCCACCACACCCTTGACAAAATTGAGGTACTTAGGCATCATATCATGGAATTCATC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879001614 Functional Loss SNV dbSNP153 33..33 33 - - - 42678 RMVar_ID_42678 Human_SNP_ID_22901858 A-to-I Human chr1 + 91643958 91643958 91643958 TTGACCCTGATGCAAAGGTGGAAGAAGAACCCAAAGAAGAACTTGAAGACACAACAGAAGACACA TTGACCCTGATGCAAAGGTGGAAGAAGAACCCGAAGAAGAACTTGAAGACACAACAGAAGACACA A G HSP90B3P Ensembl:ENSG00000203914 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879014051 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8241196 Human_miRNA_ID_1897619 42679 RMVar_ID_42679 Human_SNP_ID_22950785 A-to-I Human chr1 - 91853952 91853952 91853952 CAGGCTGGAGTGCAGTAGCATGATCTCAGCTCACTGCAACCTCCGCCTCCCGGGTTCGAGTGATT CAGGCTGGAGTGCAGTAGCATGATCTCAGCTCGCTGCAACCTCCGCCTCCCGGGTTCGAGTGATT T C TGFBR3 Ensembl:ENSG00000069702 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946728295 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94859,RMVar_hsa_circ_134483 42680 RMVar_ID_42680 Human_SNP_ID_23019246 A-to-I Human chr1 + 92133798 92133798 92133798 CGAGACCATCCTGGCTAACACGGTGAAACCCCATCTCTACTAAAAATACAAAAAATTAGCCGGGC CGAGACCATCCTGGCTAACACGGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTAGCCGGGC A G BTBD8 Ensembl:ENSG00000189195 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1314700150 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_98964 RMVar_hsa_circ_89311,RMVar_hsa_circ_287943,RMVar_hsa_circ_61793,RMVar_hsa_circ_86384,RMVar_hsa_circ_11970,RMVar_hsa_circ_134503,RMVar_hsa_circ_134505,RMVar_hsa_circ_134504,RMVar_hsa_circ_60044,RMVar_hsa_circ_362099,RMVar_hsa_circ_134508,RMVar_hsa_circ_350580 42681 RMVar_ID_42681 Human_SNP_ID_23049741 A-to-I Human chr1 - 92259986 92259986 92259986 TCACACCTGTAATCCCAGCTCTTTGGAAGGCCAAGGCGGGCGGTTCATGAAGTCAGGAGATCAAG TCACACCTGTAATCCCAGCTCTTTGGAAGGCCGAGGCGGGCGGTTCATGAAGTCAGGAGATCAAG T C GLMN Ensembl:ENSG00000174842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1008527966 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_134514,RMVar_hsa_circ_16710,RMVar_hsa_circ_301606,RMVar_hsa_circ_349620,RMVar_hsa_circ_292299,RMVar_hsa_circ_134515,RMVar_hsa_circ_134516 42682 RMVar_ID_42682 Human_SNP_ID_23052985 A-to-I Human chr1 - 92273742 92273742 92273742 TTTTAAAAAGGGTATCTTAGGCTGGGCACGGTAGCTCCCGCTTGTAGGCCCAGGCCTTTGGGAGG TTTTAAAAAGGGTATCTTAGGCTGGGCACGGTCGCTCCCGCTTGTAGGCCCAGGCCTTTGGGAGG T G GLMN Ensembl:ENSG00000174842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs764580705 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_692,RMVar_hsa_circ_349620,RMVar_hsa_circ_292299,RMVar_hsa_circ_134515,RMVar_hsa_circ_134516,RMVar_hsa_circ_37586,RMVar_hsa_circ_304526,RMVar_hsa_circ_32242,RMVar_hsa_circ_134518,RMVar_hsa_circ_985,RMVar_hsa_circ_134522,RMVar_hsa_circ_275426,RMVar_hsa_circ_296044,RMVar_hsa_circ_134523,RMVar_hsa_circ_314222,RMVar_hsa_circ_134521,RMVar_hsa_circ_134524 42683 RMVar_ID_42683 Human_SNP_ID_23053421 A-to-I Human chr1 - 92276220 92276220 92276220 ATATGTAAATGTGTATATATATTTTTTGAGATAGGGTCTTGCTCTGTGGCCTAGGCTGGAGTGCA ATATGTAAATGTGTATATATATTTTTTGAGATGGGGTCTTGCTCTGTGGCCTAGGCTGGAGTGCA T C GLMN Ensembl:ENSG00000174842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1397835205 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1756795,Human_RBP_ID_11152360 RMVar_hsa_circ_692,RMVar_hsa_circ_349620,RMVar_hsa_circ_292299,RMVar_hsa_circ_134515,RMVar_hsa_circ_134516,RMVar_hsa_circ_37586,RMVar_hsa_circ_304526,RMVar_hsa_circ_32242,RMVar_hsa_circ_134518,RMVar_hsa_circ_985,RMVar_hsa_circ_134522,RMVar_hsa_circ_275426,RMVar_hsa_circ_296044,RMVar_hsa_circ_134523,RMVar_hsa_circ_314222,RMVar_hsa_circ_134521,RMVar_hsa_circ_134524 42684 RMVar_ID_42684 Human_SNP_ID_23053512 A-to-I Human chr1 - 92276635 92276635 92276635 TTTTTGAGACAGGGTTTCACTCCCATTGCCCAAGCTGGAGTGAAGAGGCATGATGTCGGCTCACT TTTTTGAGACAGGGTTTCACTCCCATTGCCCAGGCTGGAGTGAAGAGGCATGATGTCGGCTCACT T C GLMN Ensembl:ENSG00000174842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs546200517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11152376 RMVar_hsa_circ_692,RMVar_hsa_circ_349620,RMVar_hsa_circ_292299,RMVar_hsa_circ_134515,RMVar_hsa_circ_134516,RMVar_hsa_circ_37586,RMVar_hsa_circ_304526,RMVar_hsa_circ_32242,RMVar_hsa_circ_134518,RMVar_hsa_circ_985,RMVar_hsa_circ_134522,RMVar_hsa_circ_275426,RMVar_hsa_circ_296044,RMVar_hsa_circ_134523,RMVar_hsa_circ_314222,RMVar_hsa_circ_134521,RMVar_hsa_circ_134524 42685 RMVar_ID_42685 Human_SNP_ID_23061393 A-to-I Human chr1 + 92309321 92309321 92309321 AAAATTAGCTGGACGTGGTGACACATGCCTGTAGTCTCAGCTACTCAGGAGGCTGAGGTAGGAGA AAAATTAGCTGGACGTGGTGACACATGCCTGTGGTCTCAGCTACTCAGGAGGCTGAGGTAGGAGA A G RPAP2 Ensembl:ENSG00000122484 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1212224591 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266985,RMVar_hsa_circ_48668,RMVar_hsa_circ_134528,RMVar_hsa_circ_265594,RMVar_hsa_circ_309207,RMVar_hsa_circ_356293,RMVar_hsa_circ_304023 42686 RMVar_ID_42686 Human_SNP_ID_23062038 A-to-I Human chr1 + 92312335 92312335 92312335 GTAGCTACTTGGGATGCTGAGACTAGAAGATCACTTGAGCATAGGAGTTCATGGTTGCAGTGAGT GTAGCTACTTGGGATGCTGAGACTAGAAGATCGCTTGAGCATAGGAGTTCATGGTTGCAGTGAGT A G RPAP2 Ensembl:ENSG00000122484 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs771534831 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8321871,Human_RBP_ID_11152764 RMVar_hsa_circ_266985,RMVar_hsa_circ_48668,RMVar_hsa_circ_134528,RMVar_hsa_circ_265594,RMVar_hsa_circ_309207,RMVar_hsa_circ_356293,RMVar_hsa_circ_304023 42687 RMVar_ID_42687 Human_SNP_ID_23064727 A-to-I Human chr1 + 92324297 92324297 92324297 TACGAGAATTTGAAAAAAGAAACTGAAAAGTTAAATCTGAGGATCAGGGAGTTTTACAGAGGACG TACGAGAATTTGAAAAAAGAAACTGAAAAGTTGAATCTGAGGATCAGGGAGTTTTACAGAGGACG A G RPAP2 Ensembl:ENSG00000122484 Protein coding CDS GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1557602027 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_980532,Human_RBP_ID_5882052,Human_RBP_ID_11152945,Human_RBP_ID_23420523 Human_Splice_Rec_95989 RMVar_hsa_circ_117007,RMVar_hsa_circ_266985,RMVar_hsa_circ_48668,RMVar_hsa_circ_134528,RMVar_hsa_circ_265594,RMVar_hsa_circ_309207,RMVar_hsa_circ_356293,RMVar_hsa_circ_304023,RMVar_hsa_circ_134529,RMVar_hsa_circ_285076,RMVar_hsa_circ_289044,RMVar_hsa_circ_353646,RMVar_hsa_circ_134530,RMVar_hsa_circ_282021,RMVar_hsa_circ_134532,RMVar_hsa_circ_57918,RMVar_hsa_circ_71804,RMVar_hsa_circ_27816,RMVar_hsa_circ_134533,RMVar_hsa_circ_134531 42688 RMVar_ID_42688 Human_SNP_ID_23080177 A-to-I Human chr1 + 92397150 92397150 92397150 GGGGCTCACACCTGTAATCCCAGCACTTTGGGAAGCCAAGATGGGCTGATTGCTTGAGTCCAGGA GGGGCTCACACCTGTAATCCCAGCACTTTGGGGAGCCAAGATGGGCTGATTGCTTGAGTCCAGGA A G RPAP2 Ensembl:ENSG00000122484 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs993478894 Functional Loss SNV dbSNP153 33..33 33 - - - 42689 RMVar_ID_42689 Human_SNP_ID_23080350 A-to-I Human chr1 + 92398034 92398034 92398034 AAACAATTAGCCGGGCATGGTGGCACACGCCTATAGTCCCAGCTACTCAGGAGGGTGAAGATCAC AAACAATTAGCCGGGCATGGTGGCACACGCCTGTAGTCCCAGCTACTCAGGAGGGTGAAGATCAC A G RPAP2 Ensembl:ENSG00000122484 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1485659309 Functional Loss SNV dbSNP153 33..33 33 - - - 42690 RMVar_ID_42690 Human_SNP_ID_23097078 A-to-I Human chr1 - 92468964 92468964 92468964 GGGCGTGGTGGCGGGCATCTGTGGTCCCAGCTACTTGGGAGGCTGAGGCGGGAGAATGGCATGAA GGGCGTGGTGGCGGGCATCTGTGGTCCCAGCTGCTTGGGAGGCTGAGGCGGGAGAATGGCATGAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs545372438 Functional Loss SNV dbSNP153 33..33 33 - - - 42691 RMVar_ID_42691 Human_SNP_ID_23099373 A-to-I Human chr1 - 92479067 92479067 92479067 GAGGCCAGGTGTTTGAGACCAGCCTGACCAACATGGTGAAACCCCATCTCTACTAAAAATACAAA GAGGCCAGGTGTTTGAGACCAGCCTGACCAACGTGGTGAAACCCCATCTCTACTAAAAATACAAA T C GFI1 Ensembl:ENSG00000162676 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs148423194 Functional Loss SNV dbSNP153 33..33 33 - - - 42692 RMVar_ID_42692 Human_SNP_ID_23099528 A-to-I Human chr1 - 92479689 92479689 92479689 GCCACTACAGCACAGCTAATTTTTGTGTTCTTAGTAGAGACGGGATTTCGCCACGTTAGCCAGGC GCCACTACAGCACAGCTAATTTTTGTGTTCTTTGTAGAGACGGGATTTCGCCACGTTAGCCAGGC T A GFI1 Ensembl:ENSG00000162676 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs113693381 Functional Loss SNV dbSNP153 33..33 33 - - - 42693 RMVar_ID_42693 Human_SNP_ID_23106842 A-to-I Human chr1 - 92509623 92509623 92509623 CACTCCTATAGTCCCACCTACTCAAGAGGCTGAGGCAGGAGGATCACTAGAGTACAGGAGTTTGG CACTCCTATAGTCCCACCTACTCAAGAGGCTGGGGCAGGAGGATCACTAGAGTACAGGAGTTTGG T C EVI5 Ensembl:ENSG00000067208 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1136570 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116196,RMVar_hsa_circ_126531,RMVar_hsa_circ_118265,RMVar_hsa_circ_134546,RMVar_hsa_circ_134548,RMVar_hsa_circ_114279,RMVar_hsa_circ_134547,RMVar_hsa_circ_134545 42694 RMVar_ID_42694 Human_SNP_ID_23109625 A-to-I Human chr1 - 92521122 92521122 92521122 CTCCGTCTGTAAAGAAAATACACAAATTAGCCAGGTGTGGTGGCCCACGCCTGTAGTCCCAGCTA CTCCGTCTGTAAAGAAAATACACAAATTAGCCGGGTGTGGTGGCCCACGCCTGTAGTCCCAGCTA T C EVI5 Ensembl:ENSG00000067208 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1346816273 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116196,RMVar_hsa_circ_126531,RMVar_hsa_circ_118265,RMVar_hsa_circ_134546,RMVar_hsa_circ_134548,RMVar_hsa_circ_114279,RMVar_hsa_circ_134547,RMVar_hsa_circ_134545 42695 RMVar_ID_42695 Human_SNP_ID_23114067 A-to-I Human chr1 - 92540548 92540548 92540548 GGGCCTGTATCTAGAATATATAAAGAACTCTTACAATTCAATTATAAAAAGATAACCCAGTTATA GGGCCTGTATCTAGAATATATAAAGAACTCTTGCAATTCAATTATAAAAAGATAACCCAGTTATA T C EVI5 Ensembl:ENSG00000067208 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232765475 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116196,RMVar_hsa_circ_126531,RMVar_hsa_circ_118265,RMVar_hsa_circ_134546,RMVar_hsa_circ_134548,RMVar_hsa_circ_114279,RMVar_hsa_circ_134547,RMVar_hsa_circ_134545 42696 RMVar_ID_42696 Human_SNP_ID_23114863 A-to-I Human chr1 - 92544144 92544144 92544144 TATTCCCCCAACCCTAGGCAACCCACTAATCTACTTTCTGTCTCTACACATTTCCCAATTCTGGA TATTCCCCCAACCCTAGGCAACCCACTAATCTGCTTTCTGTCTCTACACATTTCCCAATTCTGGA T C EVI5 Ensembl:ENSG00000067208 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs553595875 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3326053 RMVar_hsa_circ_116196,RMVar_hsa_circ_126531,RMVar_hsa_circ_118265,RMVar_hsa_circ_134546,RMVar_hsa_circ_134548,RMVar_hsa_circ_114279,RMVar_hsa_circ_134547,RMVar_hsa_circ_134545 42697 RMVar_ID_42697 Human_SNP_ID_23116971 A-to-I Human chr1 - 92551135 92551135 92551135 TGGGAGGCTGAAGTGAGAGGATCGCTTGACCCAGGAGGTTGAGGTTGCAGTGAGCCAAGATCATG TGGGAGGCTGAAGTGAGAGGATCGCTTGACCCGGGAGGTTGAGGTTGCAGTGAGCCAAGATCATG T C EVI5 Ensembl:ENSG00000067208 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1372078852 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116196,RMVar_hsa_circ_126531,RMVar_hsa_circ_118265,RMVar_hsa_circ_134549,RMVar_hsa_circ_134546,RMVar_hsa_circ_134548,RMVar_hsa_circ_114279,RMVar_hsa_circ_134547,RMVar_hsa_circ_134545 42698 RMVar_ID_42698 Human_SNP_ID_23146486 A-to-I Human chr1 - 92667102 92667102 92667102 TTTTATATTTTTTGTAGAGACAGGGTTTTGCCATGTTGTCCAGGCTGGTCTTGAACTCAAGCTCA TTTTATATTTTTTGTAGAGACAGGGTTTTGCCTTGTTGTCCAGGCTGGTCTTGAACTCAAGCTCA T A EVI5 Ensembl:ENSG00000067208 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1036843288 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49889,RMVar_hsa_circ_116196,RMVar_hsa_circ_126531,RMVar_hsa_circ_118265,RMVar_hsa_circ_134546,RMVar_hsa_circ_134548,RMVar_hsa_circ_114279,RMVar_hsa_circ_134547,RMVar_hsa_circ_134545,RMVar_hsa_circ_285258,RMVar_hsa_circ_372232,RMVar_hsa_circ_1325,RMVar_hsa_circ_38852,RMVar_hsa_circ_134553,RMVar_hsa_circ_134554,RMVar_hsa_circ_364546,RMVar_hsa_circ_268878,RMVar_hsa_circ_277071,RMVar_hsa_circ_59907,RMVar_hsa_circ_64079,RMVar_hsa_circ_360321,RMVar_hsa_circ_134555,RMVar_hsa_circ_280150,RMVar_hsa_circ_134562,RMVar_hsa_circ_134560,RMVar_hsa_circ_305423,RMVar_hsa_circ_46409,RMVar_hsa_circ_329253,RMVar_hsa_circ_368259,RMVar_hsa_circ_290238,RMVar_hsa_circ_285215,RMVar_hsa_circ_134563,RMVar_hsa_circ_68776,RMVar_hsa_circ_24645,RMVar_hsa_circ_348047,RMVar_hsa_circ_134564,RMVar_hsa_circ_300077,RMVar_hsa_circ_134565 42699 RMVar_ID_42699 Human_SNP_ID_23146487 A-to-I Human chr1 - 92667102 92667102 92667102 TTTTATATTTTTTGTAGAGACAGGGTTTTGCCATGTTGTCCAGGCTGGTCTTGAACTCAAGCTCA TTTTATATTTTTTGTAGAGACAGGGTTTTGCCGTGTTGTCCAGGCTGGTCTTGAACTCAAGCTCA T C EVI5 Ensembl:ENSG00000067208 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1036843288 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49889,RMVar_hsa_circ_116196,RMVar_hsa_circ_126531,RMVar_hsa_circ_118265,RMVar_hsa_circ_134546,RMVar_hsa_circ_134548,RMVar_hsa_circ_114279,RMVar_hsa_circ_134547,RMVar_hsa_circ_134545,RMVar_hsa_circ_285258,RMVar_hsa_circ_372232,RMVar_hsa_circ_1325,RMVar_hsa_circ_38852,RMVar_hsa_circ_134553,RMVar_hsa_circ_134554,RMVar_hsa_circ_364546,RMVar_hsa_circ_268878,RMVar_hsa_circ_277071,RMVar_hsa_circ_59907,RMVar_hsa_circ_64079,RMVar_hsa_circ_360321,RMVar_hsa_circ_134555,RMVar_hsa_circ_280150,RMVar_hsa_circ_134562,RMVar_hsa_circ_134560,RMVar_hsa_circ_305423,RMVar_hsa_circ_46409,RMVar_hsa_circ_329253,RMVar_hsa_circ_368259,RMVar_hsa_circ_290238,RMVar_hsa_circ_285215,RMVar_hsa_circ_134563,RMVar_hsa_circ_68776,RMVar_hsa_circ_24645,RMVar_hsa_circ_348047,RMVar_hsa_circ_134564,RMVar_hsa_circ_300077,RMVar_hsa_circ_134565 42700 RMVar_ID_42700 Human_SNP_ID_23146946 A-to-I Human chr1 - 92669365 92669365 92669365 TTTTGTATTTTTAGTAGAGATGGGGTTTTGCCATGTTGGCCTGGCTGGTCTCGAACTTCTGGCCT TTTTGTATTTTTAGTAGAGATGGGGTTTTGCCGTGTTGGCCTGGCTGGTCTCGAACTTCTGGCCT T C EVI5 Ensembl:ENSG00000067208 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167122725 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49889,RMVar_hsa_circ_116196,RMVar_hsa_circ_126531,RMVar_hsa_circ_118265,RMVar_hsa_circ_134546,RMVar_hsa_circ_134548,RMVar_hsa_circ_114279,RMVar_hsa_circ_134547,RMVar_hsa_circ_134545,RMVar_hsa_circ_285258,RMVar_hsa_circ_372232,RMVar_hsa_circ_1325,RMVar_hsa_circ_38852,RMVar_hsa_circ_134553,RMVar_hsa_circ_134554,RMVar_hsa_circ_364546,RMVar_hsa_circ_268878,RMVar_hsa_circ_277071,RMVar_hsa_circ_59907,RMVar_hsa_circ_64079,RMVar_hsa_circ_360321,RMVar_hsa_circ_134555,RMVar_hsa_circ_280150,RMVar_hsa_circ_134562,RMVar_hsa_circ_134560,RMVar_hsa_circ_305423,RMVar_hsa_circ_46409,RMVar_hsa_circ_329253,RMVar_hsa_circ_368259,RMVar_hsa_circ_290238,RMVar_hsa_circ_285215,RMVar_hsa_circ_134563,RMVar_hsa_circ_68776,RMVar_hsa_circ_24645,RMVar_hsa_circ_348047,RMVar_hsa_circ_134564,RMVar_hsa_circ_300077,RMVar_hsa_circ_134565 42701 RMVar_ID_42701 Human_SNP_ID_23159744 A-to-I Human chr1 - 92721551 92721551 92721551 CATCGTTTACATTAGGTATTTCTCCTAATGCTATCCCTCCCCCAGCCCTCCACCCCTTGACAGGC CATCGTTTACATTAGGTATTTCTCCTAATGCTGTCCCTCCCCCAGCCCTCCACCCCTTGACAGGC T C EVI5 Ensembl:ENSG00000067208 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1171250213 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49889,RMVar_hsa_circ_116196,RMVar_hsa_circ_118265,RMVar_hsa_circ_134548,RMVar_hsa_circ_134547,RMVar_hsa_circ_372232,RMVar_hsa_circ_1325,RMVar_hsa_circ_134554,RMVar_hsa_circ_64079,RMVar_hsa_circ_329253,RMVar_hsa_circ_134568,RMVar_hsa_circ_134567,RMVar_hsa_circ_24645,RMVar_hsa_circ_315348,RMVar_hsa_circ_334637,RMVar_hsa_circ_22145,RMVar_hsa_circ_286498,RMVar_hsa_circ_134573 42702 RMVar_ID_42702 Human_SNP_ID_23161216 A-to-I Human chr1 - 92727988 92727988 92727988 TTGTTTATCTTTAACTTTTTTTTTTTTGAGACAGGGTCGCACTCTGTCACCCAGGCTGGAGTGCA TTGTTTATCTTTAACTTTTTTTTTTTTGAGACGGGGTCGCACTCTGTCACCCAGGCTGGAGTGCA T C EVI5 Ensembl:ENSG00000067208 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1485276807 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49889,RMVar_hsa_circ_116196,RMVar_hsa_circ_118265,RMVar_hsa_circ_134548,RMVar_hsa_circ_134547,RMVar_hsa_circ_372232,RMVar_hsa_circ_1325,RMVar_hsa_circ_134554,RMVar_hsa_circ_64079,RMVar_hsa_circ_329253,RMVar_hsa_circ_134568,RMVar_hsa_circ_134567,RMVar_hsa_circ_24645,RMVar_hsa_circ_315348,RMVar_hsa_circ_334637,RMVar_hsa_circ_91921,RMVar_hsa_circ_22145,RMVar_hsa_circ_286498,RMVar_hsa_circ_134573,RMVar_hsa_circ_134574 42703 RMVar_ID_42703 Human_SNP_ID_23162257 A-to-I Human chr1 - 92732650 92732650 92732650 GTGATCCGCCCTCCTCAGCCTCCCAAAGTGCCAGGATTACAGACGTGAGCCACCGTGCCCAGCCT GTGATCCGCCCTCCTCAGCCTCCCAAAGTGCCTGGATTACAGACGTGAGCCACCGTGCCCAGCCT T A EVI5 Ensembl:ENSG00000067208 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1276112517 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49889,RMVar_hsa_circ_116196,RMVar_hsa_circ_118265,RMVar_hsa_circ_134548,RMVar_hsa_circ_134547,RMVar_hsa_circ_372232,RMVar_hsa_circ_1325,RMVar_hsa_circ_134554,RMVar_hsa_circ_64079,RMVar_hsa_circ_329253,RMVar_hsa_circ_134568,RMVar_hsa_circ_134567,RMVar_hsa_circ_24645,RMVar_hsa_circ_315348,RMVar_hsa_circ_334637,RMVar_hsa_circ_91921,RMVar_hsa_circ_22145,RMVar_hsa_circ_286498,RMVar_hsa_circ_134573,RMVar_hsa_circ_91032,RMVar_hsa_circ_134574,RMVar_hsa_circ_134575 42704 RMVar_ID_42704 Human_SNP_ID_23174394 A-to-I Human chr1 - 92781427 92781427 92781427 AACACTGCAACCTCCGCCTCCTGTGCTCAAGCATTCCTCCCACCTCAGCCTCCTGAGTAGCTGTG AACACTGCAACCTCCGCCTCCTGTGCTCAAGCTTTCCTCCCACCTCAGCCTCCTGAGTAGCTGTG T A EVI5 Ensembl:ENSG00000067208 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973888551 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116196,RMVar_hsa_circ_134548,RMVar_hsa_circ_81207,RMVar_hsa_circ_134577 42705 RMVar_ID_42705 Human_SNP_ID_23174395 A-to-I Human chr1 - 92781427 92781427 92781427 AACACTGCAACCTCCGCCTCCTGTGCTCAAGCATTCCTCCCACCTCAGCCTCCTGAGTAGCTGTG AACACTGCAACCTCCGCCTCCTGTGCTCAAGCGTTCCTCCCACCTCAGCCTCCTGAGTAGCTGTG T C EVI5 Ensembl:ENSG00000067208 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973888551 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116196,RMVar_hsa_circ_134548,RMVar_hsa_circ_81207,RMVar_hsa_circ_134577 42706 RMVar_ID_42706 Human_SNP_ID_23189556 A-to-I Human chr1 + 92839896 92839896 92839896 AGGATCTTGTTCTGTTTCCTGGGCTGGGGTGCAATGGCACAATTATAGCTCATTGCAACTTCAGA AGGATCTTGTTCTGTTTCCTGGGCTGGGGTGCGATGGCACAATTATAGCTCATTGCAACTTCAGA A G RPL5 Ensembl:ENSG00000122406 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1346362028 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5883318,Human_RBP_ID_11156709 RMVar_hsa_circ_83856,RMVar_hsa_circ_134579,RMVar_hsa_circ_86789,RMVar_hsa_circ_92143,RMVar_hsa_circ_134580,RMVar_hsa_circ_63888,RMVar_hsa_circ_94896,RMVar_hsa_circ_82928,RMVar_hsa_circ_134581,RMVar_hsa_circ_87915,RMVar_hsa_circ_134582,RMVar_hsa_circ_126564,RMVar_hsa_circ_134583,RMVar_hsa_circ_134586,RMVar_hsa_circ_96767,RMVar_hsa_circ_134587,RMVar_hsa_circ_134588 42707 RMVar_ID_42707 Human_SNP_ID_23189655 A-to-I Human chr1 + 92840208 92840204 92840208 GGCTAATTAGTTTTTTTATGGAGACAGGTCTCACTGTGTTGCCTTAGCTGGTCTCAAACTCCTGG GGCTAATTAGTTTTTTTATGGAGACAGGT____CTGTGTTGCCTTAGCTGGTCTCAAACTCCTGG TCTCA T RPL5 Ensembl:ENSG00000122406 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1295578634 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_5883329,Human_RBP_ID_11156734 RMVar_hsa_circ_83856,RMVar_hsa_circ_134579,RMVar_hsa_circ_86789,RMVar_hsa_circ_92143,RMVar_hsa_circ_134580,RMVar_hsa_circ_63888,RMVar_hsa_circ_94896,RMVar_hsa_circ_82928,RMVar_hsa_circ_134581,RMVar_hsa_circ_87915,RMVar_hsa_circ_134582,RMVar_hsa_circ_126564,RMVar_hsa_circ_134583,RMVar_hsa_circ_134586,RMVar_hsa_circ_96767,RMVar_hsa_circ_134587,RMVar_hsa_circ_134588 42708 RMVar_ID_42708 Human_SNP_ID_23189674 A-to-I Human chr1 + 92840263 92840263 92840263 AAACTCCTGGGCTGAAGTGATCCTCCCACTTCAGACTCCCAAAGTGCTTGAGATTACAGGCATGA AAACTCCTGGGCTGAAGTGATCCTCCCACTTCGGACTCCCAAAGTGCTTGAGATTACAGGCATGA A G RPL5 Ensembl:ENSG00000122406 Protein coding intron GSE107867 ASD brains,frontal_cortex;ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1184411541 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11156738 RMVar_hsa_circ_83856,RMVar_hsa_circ_134579,RMVar_hsa_circ_86789,RMVar_hsa_circ_92143,RMVar_hsa_circ_134580,RMVar_hsa_circ_63888,RMVar_hsa_circ_94896,RMVar_hsa_circ_82928,RMVar_hsa_circ_134581,RMVar_hsa_circ_87915,RMVar_hsa_circ_134582,RMVar_hsa_circ_126564,RMVar_hsa_circ_134583,RMVar_hsa_circ_134586,RMVar_hsa_circ_96767,RMVar_hsa_circ_134587,RMVar_hsa_circ_134588 42709 RMVar_ID_42709 Human_SNP_ID_23196122 A-to-I Human chr1 - 92866226 92866226 92866226 CTGGTGGCACATGCCTATAATCGCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCCG CTGGTGGCACATGCCTATAATCGCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCCG T C DIPK1A Ensembl:ENSG00000154511 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs140381636 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_312624,RMVar_hsa_circ_134595,RMVar_hsa_circ_134596,RMVar_hsa_circ_347671 42710 RMVar_ID_42710 Human_SNP_ID_23196124 A-to-I Human chr1 - 92866242 92866234 92866243 CAAGAATTAGCCGGGCCTGGTGGCACATGCCTATAATCGCAGCTACTCAGGAGGCTGAGGCAGGA CAAGAATTAGCCGGGCCTGGTGGCACATGCC_________AGCTACTCAGGAGGCTGAGGCAGGA TGCGATTATA T DIPK1A Ensembl:ENSG00000154511 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1194411422 Functional Loss DEL dbSNP153 32..40 33 - - - RMVar_hsa_circ_312624,RMVar_hsa_circ_134595,RMVar_hsa_circ_134596,RMVar_hsa_circ_347671 42711 RMVar_ID_42711 Human_SNP_ID_23196129 A-to-I Human chr1 - 92866239 92866239 92866239 GAATTAGCCGGGCCTGGTGGCACATGCCTATAATCGCAGCTACTCAGGAGGCTGAGGCAGGAGAA GAATTAGCCGGGCCTGGTGGCACATGCCTATAGTCGCAGCTACTCAGGAGGCTGAGGCAGGAGAA T C DIPK1A Ensembl:ENSG00000154511 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1283081637 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_312624,RMVar_hsa_circ_134595,RMVar_hsa_circ_134596,RMVar_hsa_circ_347671 42712 RMVar_ID_42712 Human_SNP_ID_23196130 A-to-I Human chr1 - 92866240 92866240 92866240 AGAATTAGCCGGGCCTGGTGGCACATGCCTATAATCGCAGCTACTCAGGAGGCTGAGGCAGGAGA AGAATTAGCCGGGCCTGGTGGCACATGCCTATCATCGCAGCTACTCAGGAGGCTGAGGCAGGAGA T G DIPK1A Ensembl:ENSG00000154511 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1557460075 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_312624,RMVar_hsa_circ_134595,RMVar_hsa_circ_134596,RMVar_hsa_circ_347671 42713 RMVar_ID_42713 Human_SNP_ID_23196132 A-to-I Human chr1 - 92866242 92866242 92866242 CAAGAATTAGCCGGGCCTGGTGGCACATGCCTATAATCGCAGCTACTCAGGAGGCTGAGGCAGGA CAAGAATTAGCCGGGCCTGGTGGCACATGCCTGTAATCGCAGCTACTCAGGAGGCTGAGGCAGGA T C DIPK1A Ensembl:ENSG00000154511 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1377363705 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_312624,RMVar_hsa_circ_134595,RMVar_hsa_circ_134596,RMVar_hsa_circ_347671 42714 RMVar_ID_42714 Human_SNP_ID_23254413 A-to-I Human chr1 + 93116703 93116703 93116703 TTTAAGTTTTTTTGTGGAAATGGAGTCTTGCTATTTGTCCACGTTGGTCTCCAACTCTTGGCCTC TTTAAGTTTTTTTGTGGAAATGGAGTCTTGCTGTTTGTCCACGTTGGTCTCCAACTCTTGGCCTC A G MTF2 Ensembl:ENSG00000143033 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs997870936 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2188,RMVar_hsa_circ_287532,RMVar_hsa_circ_301696,RMVar_hsa_circ_16463,RMVar_hsa_circ_134597,RMVar_hsa_circ_134598,RMVar_hsa_circ_28811,RMVar_hsa_circ_14022,RMVar_hsa_circ_134602,RMVar_hsa_circ_365254,RMVar_hsa_circ_373601,RMVar_hsa_circ_134603 42715 RMVar_ID_42715 Human_SNP_ID_23257119 A-to-I Human chr1 + 93128296 93128296 93128296 GTAGAACATTTTGGTTGGGCGTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAAGCCGAGGC GTAGAACATTTTGGTTGGGCGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAAGCCGAGGC A G MTF2 Ensembl:ENSG00000143033 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs189490249 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11158642 RMVar_hsa_circ_964,RMVar_hsa_circ_68849,RMVar_hsa_circ_134604,RMVar_hsa_circ_292912,RMVar_hsa_circ_13601 42716 RMVar_ID_42716 Human_SNP_ID_23264916 A-to-I Human chr1 - 93162488 93162488 93162488 GGTTCAAGCAGTTCTCCTGCCTCGGCTTCCCAAGTAGCTGGGATTACAGGTGTGTGCCACCATGG GGTTCAAGCAGTTCTCCTGCCTCGGCTTCCCAGGTAGCTGGGATTACAGGTGTGTGCCACCATGG T C TMED5 Ensembl:ENSG00000117500 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs373734846 Functional Loss SNV dbSNP153 33..33 33 - - - 42717 RMVar_ID_42717 Human_SNP_ID_23272744 A-to-I Human chr1 + 93196256 93196256 93196256 AAGGTGAAAGGGATTGCTTGAGCCTAGGAGGCAGAGATTACAGTGAGCCAAGATTGTGCCATTGC AAGGTGAAAGGGATTGCTTGAGCCTAGGAGGCGGAGATTACAGTGAGCCAAGATTGTGCCATTGC A G CCDC18 Ensembl:ENSG00000122483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1396069707 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60118,RMVar_hsa_circ_92842,RMVar_hsa_circ_134605,RMVar_hsa_circ_134607,RMVar_hsa_circ_353083,RMVar_hsa_circ_134609,RMVar_hsa_circ_355809,RMVar_hsa_circ_360741,RMVar_hsa_circ_367955,RMVar_hsa_circ_357520,RMVar_hsa_circ_344660,RMVar_hsa_circ_352013,RMVar_hsa_circ_339136,RMVar_hsa_circ_291652,RMVar_hsa_circ_322437,RMVar_hsa_circ_330065,RMVar_hsa_circ_296184,RMVar_hsa_circ_278561,RMVar_hsa_circ_61081,RMVar_hsa_circ_61338,RMVar_hsa_circ_25736,RMVar_hsa_circ_134610,RMVar_hsa_circ_134612,RMVar_hsa_circ_134611,RMVar_hsa_circ_71191,RMVar_hsa_circ_75110,RMVar_hsa_circ_337045,RMVar_hsa_circ_352103,RMVar_hsa_circ_362170,RMVar_hsa_circ_347359,RMVar_hsa_circ_266059,RMVar_hsa_circ_50515,RMVar_hsa_circ_60417 42718 RMVar_ID_42718 Human_SNP_ID_23279600 A-to-I Human chr1 + 93226637 93226637 93226637 CTCACTTGAACCTCTGCCTCCTGGGTTCAAGCAATTCTTGTGCCTCAGCCTCCTGTGTAGCTAGG CTCACTTGAACCTCTGCCTCCTGGGTTCAAGCGATTCTTGTGCCTCAGCCTCCTGTGTAGCTAGG A G CCDC18 Ensembl:ENSG00000122483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1204402246 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50772,RMVar_hsa_circ_60118,RMVar_hsa_circ_92842,RMVar_hsa_circ_353083,RMVar_hsa_circ_134609,RMVar_hsa_circ_355809,RMVar_hsa_circ_367955,RMVar_hsa_circ_339136,RMVar_hsa_circ_322437,RMVar_hsa_circ_61081,RMVar_hsa_circ_71024,RMVar_hsa_circ_61338,RMVar_hsa_circ_352103,RMVar_hsa_circ_347359,RMVar_hsa_circ_266059,RMVar_hsa_circ_60417,RMVar_hsa_circ_329335,RMVar_hsa_circ_134614,RMVar_hsa_circ_372568,RMVar_hsa_circ_362352,RMVar_hsa_circ_377863,RMVar_hsa_circ_333149,RMVar_hsa_circ_35777,RMVar_hsa_circ_298656,RMVar_hsa_circ_134616,RMVar_hsa_circ_324930,RMVar_hsa_circ_134621,RMVar_hsa_circ_73399,RMVar_hsa_circ_368503,RMVar_hsa_circ_355904,RMVar_hsa_circ_67100,RMVar_hsa_circ_280678,RMVar_hsa_circ_59405,RMVar_hsa_circ_329456,RMVar_hsa_circ_364796,RMVar_hsa_circ_350075,RMVar_hsa_circ_358641,RMVar_hsa_circ_365638,RMVar_hsa_circ_320875,RMVar_hsa_circ_7930,RMVar_hsa_circ_73793,RMVar_hsa_circ_58012,RMVar_hsa_circ_134622,RMVar_hsa_circ_336430,RMVar_hsa_circ_134623 42719 RMVar_ID_42719 Human_SNP_ID_23292262 A-to-I Human chr1 - 93282222 93282222 93282222 CTCCCACCTCAGCCTCCTGAATAGCTAGGACTATAGCACACACCACCATGCCTGGTTGATTTTTT CTCCCACCTCAGCCTCCTGAATAGCTAGGACTGTAGCACACACCACCATGCCTGGTTGATTTTTT T C CCDC18-AS1 Ensembl:ENSG00000223745 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs550701858 Functional Loss SNV dbSNP153 33..33 33 - - - 42720 RMVar_ID_42720 Human_SNP_ID_23292264 A-to-I Human chr1 - 93282228 93282228 93282228 GCAATCCTCCCACCTCAGCCTCCTGAATAGCTAGGACTATAGCACACACCACCATGCCTGGTTGA GCAATCCTCCCACCTCAGCCTCCTGAATAGCTTGGACTATAGCACACACCACCATGCCTGGTTGA T A CCDC18-AS1 Ensembl:ENSG00000223745 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs960922531 Functional Loss SNV dbSNP153 33..33 33 - - - 42721 RMVar_ID_42721 Human_SNP_ID_23296147 A-to-I Human chr1 - 93300714 93300714 93300714 TTTTATATTTTTAGTAGAGTCGGGGTTTCTCCATGTTGATCAGGCTGGTCTTGAACTCTCGACCT TTTTATATTTTTAGTAGAGTCGGGGTTTCTCCGTGTTGATCAGGCTGGTCTTGAACTCTCGACCT T C CCDC18-AS1 Ensembl:ENSG00000223745 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1483609402 Functional Loss SNV dbSNP153 33..33 33 - - - 42722 RMVar_ID_42722 Human_SNP_ID_23296164 A-to-I Human chr1 - 93300784 93300784 93300784 TCAAGTGATTCTCCTGCTTCAGCCTTCCGAGTAGCTGGAATTACAGGCATGTGCCACCATGCCCA TCAAGTGATTCTCCTGCTTCAGCCTTCCGAGTGGCTGGAATTACAGGCATGTGCCACCATGCCCA T C CCDC18-AS1 Ensembl:ENSG00000223745 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1458610477 Functional Loss SNV dbSNP153 33..33 33 - - - 42723 RMVar_ID_42723 Human_SNP_ID_23297963 A-to-I Human chr1 - 93309759 93309759 93309759 GAAACTCACTCTGTCACTCAGGCTGGAGTGCAATGGCACGATCTCGGCTCACTGCAACCTCTGCC GAAACTCACTCTGTCACTCAGGCTGGAGTGCAGTGGCACGATCTCGGCTCACTGCAACCTCTGCC T C CCDC18-AS1 Ensembl:ENSG00000223745 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs781036460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_96824,Human_Splice_Rec_96825,Human_Splice_Rec_96851,Human_Splice_Rec_96868,Human_Splice_Rec_96869,Human_Splice_Rec_96876,Human_Splice_Rec_96877,Human_Splice_Rec_96914 RMVar_hsa_circ_272541,RMVar_hsa_circ_321210,RMVar_hsa_circ_360562,RMVar_hsa_circ_300151,RMVar_hsa_circ_134629,RMVar_hsa_circ_134630,RMVar_hsa_circ_134628 42724 RMVar_ID_42724 Human_SNP_ID_23299162 A-to-I Human chr1 - 93315217 93315217 93315217 GTTGGCCGGGCTGGTCTTGAAGTCCTGACCTCAGGTGATTCACCTACCTCAGCTTCCCGACGTAC GTTGGCCGGGCTGGTCTTGAAGTCCTGACCTCGGGTGATTCACCTACCTCAGCTTCCCGACGTAC T C CCDC18-AS1 Ensembl:ENSG00000223745 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs939003201 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_96834,Human_Splice_Rec_96835,Human_Splice_Rec_96855,Human_Splice_Rec_96867,Human_Splice_Rec_96963 RMVar_hsa_circ_272541,RMVar_hsa_circ_360562,RMVar_hsa_circ_300151,RMVar_hsa_circ_134629,RMVar_hsa_circ_134630 42725 RMVar_ID_42725 Human_SNP_ID_23299192 A-to-I Human chr1 - 93315351 93315351 93315351 CGGCTCACTGCAACCTCTGCCTCCCAGTTTCAAGAGATTCTCTTGCCTCAGCCTCCCAAGTAGCT CGGCTCACTGCAACCTCTGCCTCCCAGTTTCAGGAGATTCTCTTGCCTCAGCCTCCCAAGTAGCT T C CCDC18-AS1 Ensembl:ENSG00000223745 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs953709078 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_272541,RMVar_hsa_circ_360562,RMVar_hsa_circ_300151,RMVar_hsa_circ_134629,RMVar_hsa_circ_134630 42726 RMVar_ID_42726 Human_SNP_ID_23303161 A-to-I Human chr1 - 93333356 93333356 93333356 TCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGAACTACAGGCACGCACCACAACACCCA TCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTTGCTGGAACTACAGGCACGCACCACAACACCCA T A CCDC18-AS1 Ensembl:ENSG00000223745 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886764124 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_300151,RMVar_hsa_circ_73408,RMVar_hsa_circ_345309 42727 RMVar_ID_42727 Human_SNP_ID_23303168 A-to-I Human chr1 - 93333392 93333392 93333392 ACGATCTCAGCTCACTGCAACCTCCACCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCA ACGATCTCAGCTCACTGCAACCTCCACCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCA T C CCDC18-AS1 Ensembl:ENSG00000223745 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1342165905 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_3192416 RMVar_hsa_circ_300151,RMVar_hsa_circ_73408,RMVar_hsa_circ_345309 42728 RMVar_ID_42728 Human_SNP_ID_23303331 A-to-I Human chr1 - 93334141 93334141 93334141 GGATGATTGCTTGAGCCCAGGAGTTTGAGGCCACAGTAAGCTATGATTGCACTATTGCACTCTAG GGATGATTGCTTGAGCCCAGGAGTTTGAGGCCCCAGTAAGCTATGATTGCACTATTGCACTCTAG T G CCDC18-AS1 Ensembl:ENSG00000223745 lincRNA intron GSE38233;GSE107867 cultured B-cells;ASD brains,Fragile X samples from NIH NeuroBioBank - 24183664,30559470 RNA-Seq:(High) rs948485450 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_300151,RMVar_hsa_circ_73408,RMVar_hsa_circ_345309 42729 RMVar_ID_42729 Human_SNP_ID_23303334 A-to-I Human chr1 - 93334155 93334155 93334155 AGGAGGCTGAGATGGGATGATTGCTTGAGCCCAGGAGTTTGAGGCCACAGTAAGCTATGATTGCA AGGAGGCTGAGATGGGATGATTGCTTGAGCCCGGGAGTTTGAGGCCACAGTAAGCTATGATTGCA T C CCDC18-AS1 Ensembl:ENSG00000223745 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs970211044 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_300151,RMVar_hsa_circ_73408,RMVar_hsa_circ_345309 42730 RMVar_ID_42730 Human_SNP_ID_23303342 A-to-I Human chr1 - 93334203 93334203 93334203 AAAAAAAAAGCCAGGCATAATGGCGTGTGCCTATAGTCCTAGCTACTCAGGAGGCTGAGATGGGA AAAAAAAAAGCCAGGCATAATGGCGTGTGCCTGTAGTCCTAGCTACTCAGGAGGCTGAGATGGGA T C CCDC18-AS1 Ensembl:ENSG00000223745 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs142809919 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_300151,RMVar_hsa_circ_73408,RMVar_hsa_circ_345309 42731 RMVar_ID_42731 Human_SNP_ID_23303651 A-to-I Human chr1 - 93335408 93335408 93335408 CGGGTTTCACCATGTTGGTAAGGCTGATCTCAAACTCGTGACCTTGTGATCTGCTCACCTTGGCC CGGGTTTCACCATGTTGGTAAGGCTGATCTCAGACTCGTGACCTTGTGATCTGCTCACCTTGGCC T C CCDC18-AS1 Ensembl:ENSG00000223745 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1178963375 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_300151,RMVar_hsa_circ_73408,RMVar_hsa_circ_345309 42732 RMVar_ID_42732 Human_SNP_ID_23303667 A-to-I Human chr1 - 93335479 93335479 93335479 AGTCTCCTGAGTAGCTGGGATTACAGGCGCGCACCACCACGCCCGGCTAATTTTTGTATTTTTAG AGTCTCCTGAGTAGCTGGGATTACAGGCGCGCGCCACCACGCCCGGCTAATTTTTGTATTTTTAG T C CCDC18-AS1 Ensembl:ENSG00000223745 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1414519763 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_103957 RMVar_hsa_circ_300151,RMVar_hsa_circ_73408,RMVar_hsa_circ_345309 42733 RMVar_ID_42733 Human_SNP_ID_23303686 A-to-I Human chr1 - 93335554 93335554 93335554 CAGGCTGAAGTGCAGTGGTGTAATCTCGGCTCACTGCAACCTCCGCCTCCCGGGTTCAGGCAGTT CAGGCTGAAGTGCAGTGGTGTAATCTCGGCTCGCTGCAACCTCCGCCTCCCGGGTTCAGGCAGTT T C CCDC18-AS1 Ensembl:ENSG00000223745 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1176920432 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_103957 RMVar_hsa_circ_300151,RMVar_hsa_circ_73408,RMVar_hsa_circ_345309 42734 RMVar_ID_42734 Human_SNP_ID_23303690 A-to-I Human chr1 - 93335564 93335564 93335564 CTCTGTCACCCAGGCTGAAGTGCAGTGGTGTAATCTCGGCTCACTGCAACCTCCGCCTCCCGGGT CTCTGTCACCCAGGCTGAAGTGCAGTGGTGTAGTCTCGGCTCACTGCAACCTCCGCCTCCCGGGT T C CCDC18-AS1 Ensembl:ENSG00000223745 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1320217260 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_300151,RMVar_hsa_circ_73408,RMVar_hsa_circ_345309 42735 RMVar_ID_42735 Human_SNP_ID_23304284 A-to-I Human chr1 - 93337933 93337933 93337933 AGGAGACTGAGGTGGGAGGATTGATTGAGCTCAGGAGTTTGAGGCTGCAGTGAGCAATCATCATG AGGAGACTGAGGTGGGAGGATTGATTGAGCTCGGGAGTTTGAGGCTGCAGTGAGCAATCATCATG T C CCDC18-AS1 Ensembl:ENSG00000223745 lincRNA intron GSE38233;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,32596459 RNA-Seq:(High) rs531115328 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24741606 Human_miRNA_ID_3180164 RMVar_hsa_circ_300151,RMVar_hsa_circ_73408,RMVar_hsa_circ_345309 42736 RMVar_ID_42736 Human_SNP_ID_23304291 A-to-I Human chr1 - 93337969 93337969 93337969 AGGCATGGTGGCATGCACCTGTAGTCGTAGCTACTCAGGAGACTGAGGTGGGAGGATTGATTGAG AGGCATGGTGGCATGCACCTGTAGTCGTAGCTGCTCAGGAGACTGAGGTGGGAGGATTGATTGAG T C CCDC18-AS1 Ensembl:ENSG00000223745 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048423945 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5091610,Human_RBP_ID_19434105 RMVar_hsa_circ_300151,RMVar_hsa_circ_73408,RMVar_hsa_circ_345309 42737 RMVar_ID_42737 Human_SNP_ID_23304299 A-to-I Human chr1 - 93338001 93338001 93338001 TCTCTACTAAAAAGTAAAAAAAAAATTTAGTCAGGCATGGTGGCATGCACCTGTAGTCGTAGCTA TCTCTACTAAAAAGTAAAAAAAAAATTTAGTCGGGCATGGTGGCATGCACCTGTAGTCGTAGCTA T C CCDC18-AS1 Ensembl:ENSG00000223745 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs937561388 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5091610 RMVar_hsa_circ_300151,RMVar_hsa_circ_73408,RMVar_hsa_circ_345309 42738 RMVar_ID_42738 Human_SNP_ID_23336153 A-to-I Human chr1 + 93470210 93470210 93470210 GCTGGAGTATAGTGATGCTGTCATAGCACAGTAACCTCAAACTCCTGGGCTCAAGTGAGCATCCT GCTGGAGTATAGTGATGCTGTCATAGCACAGTGACCTCAAACTCCTGGGCTCAAGTGAGCATCCT A G FNBP1L Ensembl:ENSG00000137942 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1418581759 Functional Loss SNV dbSNP153 33..33 33 - - - 42739 RMVar_ID_42739 Human_SNP_ID_23336154 A-to-I Human chr1 + 93470216 93470216 93470216 GTATAGTGATGCTGTCATAGCACAGTAACCTCAAACTCCTGGGCTCAAGTGAGCATCCTATCTTA GTATAGTGATGCTGTCATAGCACAGTAACCTCCAACTCCTGGGCTCAAGTGAGCATCCTATCTTA A C FNBP1L Ensembl:ENSG00000137942 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1034043933 Functional Loss SNV dbSNP153 33..33 33 - - - 42740 RMVar_ID_42740 Human_SNP_ID_23343849 A-to-I Human chr1 + 93503174 93503174 93503174 ATTTATAAGGGAAAGAGGTTTAATTGACTCACAGTTCAGCATGGCTGGGGAGGCCTCAGTAAACT ATTTATAAGGGAAAGAGGTTTAATTGACTCACGGTTCAGCATGGCTGGGGAGGCCTCAGTAAACT A G FNBP1L Ensembl:ENSG00000137942 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1212056645 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_134637,RMVar_hsa_circ_304555,RMVar_hsa_circ_347269,RMVar_hsa_circ_362797,RMVar_hsa_circ_356001,RMVar_hsa_circ_323097,RMVar_hsa_circ_34004,RMVar_hsa_circ_16524,RMVar_hsa_circ_134638 42741 RMVar_ID_42741 Human_SNP_ID_23344131 A-to-I Human chr1 + 93504443 93504443 93504443 TGAGTCTGAAGCCTCCCCAGCCATGTGGAACTATAATTCCAATTAAACCTCTTTTTCCTCCCTGT TGAGTCTGAAGCCTCCCCAGCCATGTGGAACTGTAATTCCAATTAAACCTCTTTTTCCTCCCTGT A G FNBP1L Ensembl:ENSG00000137942 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1275134861 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11163664,Human_RBP_ID_17761558 RMVar_hsa_circ_134637,RMVar_hsa_circ_304555,RMVar_hsa_circ_347269,RMVar_hsa_circ_362797,RMVar_hsa_circ_356001,RMVar_hsa_circ_323097,RMVar_hsa_circ_34004,RMVar_hsa_circ_16524,RMVar_hsa_circ_134638 42742 RMVar_ID_42742 Human_SNP_ID_23372188 A-to-I Human chr1 - 93619227 93619227 93619227 AAAACCATGGCTTTGGCTGGGCACAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAG AAAACCATGGCTTTGGCTGGGCACAGTGGCTCTCGCCTGTAATCCCAGCACTTTGGGAGGCCGAG T A BCAR3 Ensembl:ENSG00000137936 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs149944279 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23303788 RMVar_hsa_circ_42663,RMVar_hsa_circ_25521 42743 RMVar_ID_42743 Human_SNP_ID_23381057 A-to-I Human chr1 - 93659248 93659248 93659248 TTAACCCCATTAGGTCGAGGCTGCAGTGAACCAATGTTGCACCACTGCACTCCAGCCTGGGCAAC TTAACCCCATTAGGTCGAGGCTGCAGTGAACCGATGTTGCACCACTGCACTCCAGCCTGGGCAAC T C BCAR3 Ensembl:ENSG00000137936 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903432439 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42663,RMVar_hsa_circ_134657,RMVar_hsa_circ_293349 42744 RMVar_ID_42744 Human_SNP_ID_23431874 A-to-I Human chr1 - 93883314 93883314 93883314 GAACTAAACAATCCTCCTGCTCCAGCCTCCCAAGTTGCTGAGACTACAGGCACATGCCACCACAC GAACTAAACAATCCTCCTGCTCCAGCCTCCCAGGTTGCTGAGACTACAGGCACATGCCACCACAC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1280336471 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8322580,Human_RBP_ID_17761662 42745 RMVar_ID_42745 Human_SNP_ID_23431959 A-to-I Human chr1 - 93883663 93883663 93883663 CACACCTGGCTAACTTTTATTTTTGTAGAGACAGGATCTCGCTATGTTGCCCAGGCTGGTCTTGA CACACCTGGCTAACTTTTATTTTTGTAGAGACGGGATCTCGCTATGTTGCCCAGGCTGGTCTTGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs979439025 Functional Loss SNV dbSNP153 33..33 33 - - - 42746 RMVar_ID_42746 Human_SNP_ID_23434226 A-to-I Human chr1 - 93894075 93894075 93894075 TTTTCTATTTTTTGCAGAGACAGGGTTTCACCATGTCACCCAGGCTGGGCTTGAATTTCTGGACT TTTTCTATTTTTTGCAGAGACAGGGTTTCACCGTGTCACCCAGGCTGGGCTTGAATTTCTGGACT T C GCLM Ensembl:ENSG00000023909 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005170122 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11165042 RMVar_hsa_circ_113802,RMVar_hsa_circ_134663 42747 RMVar_ID_42747 Human_SNP_ID_23563588 A-to-I Human chr1 + 94435457 94435457 94435457 CAGCTACTGAGGTGGGAGGATCACTTCAGCCTAGGAGATTGAGTCTGCAGTGAACTGTGATGGCA CAGCTACTGAGGTGGGAGGATCACTTCAGCCTGGGAGATTGAGTCTGCAGTGAACTGTGATGGCA A G ABCD3 Ensembl:ENSG00000117528 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs775807258 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11165921 RMVar_hsa_circ_107372,RMVar_hsa_circ_134678 42748 RMVar_ID_42748 Human_SNP_ID_23583512 A-to-I Human chr1 + 94517079 94517079 94517079 CATAGTACTACCTGCATATGGATGGCAGAGGCAACTATGAATTCAAACAGATAACAGAAGATACA CATAGTACTACCTGCATATGGATGGCAGAGGCGACTATGAATTCAAACAGATAACAGAAGATACA A G ABCD3 Ensembl:ENSG00000117528 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs748988875 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9356597,Human_RBP_ID_11166866 Human_Splice_Rec_97874,Human_Splice_Rec_97918,Human_Splice_Rec_97980,Human_Splice_Rec_97982 42749 RMVar_ID_42749 Human_SNP_ID_23742135 A-to-I Human chr1 + 95192112 95192112 95192112 GAGGTCAGGAGTTCGAGACTAGCTTGGCCAACATGGTGAAACCTCATCTCTACTAAAAATACAAA GAGGTCAGGAGTTCGAGACTAGCTTGGCCAACGTGGTGAAACCTCATCTCTACTAAAAATACAAA A G TLCD4,TLCD4-RWDD3 Ensembl:ENSG00000152078,Ensembl:ENSG00000271092 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs532486973 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_327348,RMVar_hsa_circ_134725,RMVar_hsa_circ_95568,RMVar_hsa_circ_134727,RMVar_hsa_circ_134728,RMVar_hsa_circ_99975 42750 RMVar_ID_42750 Human_SNP_ID_24115364 A-to-I Human chr1 + 96725399 96725399 96725399 CTGGCTCACTACAAGCTCCGCCTTCCGGGTTCACTCCATTCTTCTGCCTCAGCCTCCCGAGTAGC CTGGCTCACTACAAGCTCCGCCTTCCGGGTTCGCTCCATTCTTCTGCCTCAGCCTCCCGAGTAGC A G PTBP2 Ensembl:ENSG00000117569 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs972246860 Functional Loss SNV dbSNP153 33..33 33 - - - 42751 RMVar_ID_42751 Human_SNP_ID_24115570 A-to-I Human chr1 + 96726027 96726027 96726027 AACCTGCGAGGCAGAGGTTGCAGTAAGCGGAGATTGCACCACTGCACTCCAGCCTGGGCGACAGA AACCTGCGAGGCAGAGGTTGCAGTAAGCGGAGGTTGCACCACTGCACTCCAGCCTGGGCGACAGA A G PTBP2 Ensembl:ENSG00000117569 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1239003564 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9551734,Human_RBP_ID_24771103 42752 RMVar_ID_42752 Human_SNP_ID_24135597 A-to-I Human chr1 + 96798219 96798219 96798219 CTTGAGATCATGAGTTCAAAACCAGCCTGGCCAACATGGTGAAACACTGTCTCTACTAAAAATAC CTTGAGATCATGAGTTCAAAACCAGCCTGGCCCACATGGTGAAACACTGTCTCTACTAAAAATAC A C PTBP2 Ensembl:ENSG00000117569 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs887973519 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8183,RMVar_hsa_circ_134730,RMVar_hsa_circ_64332,RMVar_hsa_circ_369584,RMVar_hsa_circ_134729,RMVar_hsa_circ_336701,RMVar_hsa_circ_134738,RMVar_hsa_circ_27086,RMVar_hsa_circ_134742,RMVar_hsa_circ_45433,RMVar_hsa_circ_16515 42753 RMVar_ID_42753 Human_SNP_ID_24135960 A-to-I Human chr1 + 96799375 96799375 96799375 TGGAGTGCAATGGTGCGATCTCGGCTCACTGCAAACTCGGCCTCCCGGGTTCGTGCCATTCTTCT TGGAGTGCAATGGTGCGATCTCGGCTCACTGCCAACTCGGCCTCCCGGGTTCGTGCCATTCTTCT A C PTBP2 Ensembl:ENSG00000117569 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1055542230 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8183,RMVar_hsa_circ_134730,RMVar_hsa_circ_64332,RMVar_hsa_circ_369584,RMVar_hsa_circ_134729,RMVar_hsa_circ_336701,RMVar_hsa_circ_134738,RMVar_hsa_circ_27086,RMVar_hsa_circ_134742,RMVar_hsa_circ_45433,RMVar_hsa_circ_16515 42754 RMVar_ID_42754 Human_SNP_ID_24323994 A-to-I Human chr1 - 97546345 97546345 97546345 TCATCTTCCTTTACTGCAGCTTCATTCCCAACAACTCCATTTGCCAGCTTTTGTTTCTGTTGCTT TCATCTTCCTTTACTGCAGCTTCATTCCCAACGACTCCATTTGCCAGCTTTTGTTTCTGTTGCTT T C DPYD Ensembl:ENSG00000188641 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs959420245 Functional Loss SNV dbSNP153 33..33 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 42755 RMVar_ID_42755 Human_SNP_ID_24324094 A-to-I Human chr1 + 97546696 97546696 97546696 ACATTAATATCCATGCCATATCATGTGTGTACACTAAAAGATACAGAGGAAGTAGAGCTGAAGTT ACATTAATATCCATGCCATATCATGTGTGTACGCTAAAAGATACAGAGGAAGTAGAGCTGAAGTT A G SEC63P1 Ensembl:ENSG00000228057 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1184123778 Functional Loss SNV dbSNP153 33..33 33 - - - 42756 RMVar_ID_42756 Human_SNP_ID_24324097 A-to-I Human chr1 + 97546699 97546699 97546699 TTAATATCCATGCCATATCATGTGTGTACACTAAAAGATACAGAGGAAGTAGAGCTGAAGTTTCC TTAATATCCATGCCATATCATGTGTGTACACTGAAAGATACAGAGGAAGTAGAGCTGAAGTTTCC A G SEC63P1 Ensembl:ENSG00000228057 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1249756951 Functional Loss SNV dbSNP153 33..33 33 - - - 42757 RMVar_ID_42757 Human_SNP_ID_24433559 A-to-I Human chr1 - 97989533 97989533 97989533 TGTTTCGCTCTTATTGCCCAGGCTGGAGTGCAATGACGTGATCTTGACTCACCACAGCCTCTGCA TGTTTCGCTCTTATTGCCCAGGCTGGAGTGCAGTGACGTGATCTTGACTCACCACAGCCTCTGCA T C DPYD,MIR137HG Ensembl:ENSG00000188641,Ensembl:ENSG00000225206 Protein coding,lincRNA intron,intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs973420845 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_99134,Human_Splice_Rec_99142 RMVar_hsa_circ_134797 42758 RMVar_ID_42758 Human_SNP_ID_24441646 A-to-I Human chr1 - 98023119 98023119 98023119 CTCTGTCCTCCAGGCTGGAGTGCAGTGGTGTGATCATAGTTCACTGCAGCCTCCAACTCTTGAGA CTCTGTCCTCCAGGCTGGAGTGCAGTGGTGTGGTCATAGTTCACTGCAGCCTCCAACTCTTGAGA T C MIR137HG Ensembl:ENSG00000225206 lincRNA intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1326933744 Functional Loss SNV dbSNP153 33..33 33 - - - 42759 RMVar_ID_42759 Human_SNP_ID_24853552 A-to-I Human chr1 + 99684745 99684745 99684745 CACTATGTTGTCCAGGCTCATCTCTAACTCCTAGGCTCAAGCAATCTTCCTGCCTCAGCTTCCCA CACTATGTTGTCCAGGCTCATCTCTAACTCCTGGGCTCAAGCAATCTTCCTGCCTCAGCTTCCCA A G PALMD Ensembl:ENSG00000099260 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs150591964 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9501,RMVar_hsa_circ_78094,RMVar_hsa_circ_112420,RMVar_hsa_circ_134835,RMVar_hsa_circ_134836,RMVar_hsa_circ_8726,RMVar_hsa_circ_134837 42760 RMVar_ID_42760 Human_SNP_ID_24871957 A-to-I Human chr1 - 99763829 99763829 99763829 AGTTTCACTCTTGTTGCCCAGGCTGGAGTGCAATGGTGCCATCTCGGCTCACCTCAACCTCTGCC AGTTTCACTCTTGTTGCCCAGGCTGGAGTGCAGTGGTGCCATCTCGGCTCACCTCAACCTCTGCC T C FRRS1 Ensembl:ENSG00000156869 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1315689943 Functional Loss SNV dbSNP153 33..33 33 - - - 42761 RMVar_ID_42761 Human_SNP_ID_24893503 A-to-I Human chr1 + 99852495 99852495 99852495 GGGCTCAAGCAGTTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTGCAGGCATACATCACTATG GGGCTCAAGCAGTTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTGCAGGCATACATCACTATG A G AGL Ensembl:ENSG00000162688 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1329574140 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7641,RMVar_hsa_circ_84943,RMVar_hsa_circ_108592,RMVar_hsa_circ_134855,RMVar_hsa_circ_134856,RMVar_hsa_circ_49969 42762 RMVar_ID_42762 Human_SNP_ID_24893530 A-to-I Human chr1 + 99852559 99852559 99852559 GCCCCGCTAATTTTTTTTTTTTTTTTTTTTGTAGAAACTGGGTCTCACTATGTTGCCCAGGTTGA GCCCCGCTAATTTTTTTTTTTTTTTTTTTTGTGGAAACTGGGTCTCACTATGTTGCCCAGGTTGA A G AGL Ensembl:ENSG00000162688 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1320681069 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10486842 RMVar_hsa_circ_7641,RMVar_hsa_circ_84943,RMVar_hsa_circ_108592,RMVar_hsa_circ_134855,RMVar_hsa_circ_134856,RMVar_hsa_circ_49969 42763 RMVar_ID_42763 Human_SNP_ID_24893531 A-to-I Human chr1 + 99852559 99852559 99852559 GCCCCGCTAATTTTTTTTTTTTTTTTTTTTGTAGAAACTGGGTCTCACTATGTTGCCCAGGTTGA GCCCCGCTAATTTTTTTTTTTTTTTTTTTTGTTGAAACTGGGTCTCACTATGTTGCCCAGGTTGA A T AGL Ensembl:ENSG00000162688 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1320681069 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10486842 RMVar_hsa_circ_7641,RMVar_hsa_circ_84943,RMVar_hsa_circ_108592,RMVar_hsa_circ_134855,RMVar_hsa_circ_134856,RMVar_hsa_circ_49969 42764 RMVar_ID_42764 Human_SNP_ID_24934718 A-to-I Human chr1 + 100023951 100023951 100023951 ATCACTTGAACCCGGGAGGCAGAGGTTGCAGTAAGTGGAGATCACGCCACTGCACTCCAACCTGG ATCACTTGAACCCGGGAGGCAGAGGTTGCAGTGAGTGGAGATCACGCCACTGCACTCCAACCTGG A G AC118553.2,SLC35A3 Ensembl:ENSG00000283761,Ensembl:ENSG00000117620 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1137438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22843611,Human_RBP_ID_24564592 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 42765 RMVar_ID_42765 Human_SNP_ID_24934721 A-to-I Human chr1 + 100023962 100023962 100023962 CCGGGAGGCAGAGGTTGCAGTAAGTGGAGATCACGCCACTGCACTCCAACCTGGGCGACACAGTG CCGGGAGGCAGAGGTTGCAGTAAGTGGAGATCGCGCCACTGCACTCCAACCTGGGCGACACAGTG A G AC118553.2,SLC35A3 Ensembl:ENSG00000283761,Ensembl:ENSG00000117620 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1137440 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22843611,Human_RBP_ID_24564592 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 42766 RMVar_ID_42766 Human_SNP_ID_24934856 A-to-I Human chr1 + 100024533 100024532 100024534 AGATCGTGCCACTGCACCCCAGCCTGGGTGACAGAGCGAGACTCCGTCTCAAAAAAAAAAAAAAG AGATCGTGCCACTGCACCCCAGCCTGGGTGAC__AGCGAGACTCCGTCTCAAAAAAAAAAAAAAG CAG C AC118553.2,SLC35A3 Ensembl:ENSG00000283761,Ensembl:ENSG00000117620 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1282140063 Functional Loss DEL dbSNP153 33..34 33 - - - 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 42767 RMVar_ID_42767 Human_SNP_ID_24934916 A-to-I Human chr1 + 100024639 100024639 100024639 AAAAATAAAATACTTCTTTTTTTTTTTTTTTGAGACAGAGTCTCACTTTGTCGCCAGGCTGGAGT AAAAATAAAATACTTCTTTTTTTTTTTTTTTGTGACAGAGTCTCACTTTGTCGCCAGGCTGGAGT A T AC118553.2,SLC35A3 Ensembl:ENSG00000283761,Ensembl:ENSG00000117620 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1308908056 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11176883,Human_RBP_ID_22369418,Human_RBP_ID_26386189 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 42768 RMVar_ID_42768 Human_SNP_ID_24934919 A-to-I Human chr1 + 100024643 100024642 100024644 ATAAAATACTTCTTTTTTTTTTTTTTTGAGACAGAGTCTCACTTTGTCGCCAGGCTGGAGTGCTG ATAAAATACTTCTTTTTTTTTTTTTTTGAGAC__AGTCTCACTTTGTCGCCAGGCTGGAGTGCTG CAG C AC118553.2,SLC35A3 Ensembl:ENSG00000283761,Ensembl:ENSG00000117620 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1250410103 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_3978056,Human_RBP_ID_11176883,Human_RBP_ID_22369418,Human_RBP_ID_26386189 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 42769 RMVar_ID_42769 Human_SNP_ID_24934924 A-to-I Human chr1 + 100024669 100024669 100024669 TGAGACAGAGTCTCACTTTGTCGCCAGGCTGGAGTGCTGTGGCGCGATCTCGGCTTACTGCAACC TGAGACAGAGTCTCACTTTGTCGCCAGGCTGGGGTGCTGTGGCGCGATCTCGGCTTACTGCAACC A G AC118553.2,SLC35A3 Ensembl:ENSG00000283761,Ensembl:ENSG00000117620 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1056314276 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22369418,Human_RBP_ID_26386189 Human_Splice_Rec_99976,Human_Splice_Rec_100096,Human_Splice_Rec_100120 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 42770 RMVar_ID_42770 Human_SNP_ID_24934934 A-to-I Human chr1 + 100024718 100024718 100024718 TCGGCTTACTGCAACCTCCCACTCCCTGGTTCAAGGGATTCTCCTGCCTCAGCCTCTGAGTAGCT TCGGCTTACTGCAACCTCCCACTCCCTGGTTCGAGGGATTCTCCTGCCTCAGCCTCTGAGTAGCT A G AC118553.2,SLC35A3 Ensembl:ENSG00000283761,Ensembl:ENSG00000117620 Protein coding,Protein coding intron,intron GSE38233;GSE100210;GSE99789;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,29796672,31158229,32596459,32596459 RNA-Seq:(High) rs999819912 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557946,Human_RBP_ID_26386190 Human_Splice_Rec_99976,Human_Splice_Rec_100096,Human_Splice_Rec_100120 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 42771 RMVar_ID_42771 Human_SNP_ID_24938971 A-to-I Human chr1 + 100041835 100041835 100041835 AATCCCAGCTACCCGGGAGGCCGAGGCACGAGAATCACTTGAACCTGGGAGGCCAAGATTGCAGT AATCCCAGCTACCCGGGAGGCCGAGGCACGAGGATCACTTGAACCTGGGAGGCCAAGATTGCAGT A G MFSD14A,AC118553.2 Ensembl:ENSG00000156875,Ensembl:ENSG00000283761 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1469908102 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42772 RMVar_ID_42772 Human_SNP_ID_24939189 A-to-I Human chr1 + 100042747 100042747 100042747 CTCCTACCTTAGCCTCCTGAATAGCTGGGATTACAGGCATGTGCCATCATGCCCAGCTAATTTTT CTCCTACCTTAGCCTCCTGAATAGCTGGGATTGCAGGCATGTGCCATCATGCCCAGCTAATTTTT A G MFSD14A,AC118553.2 Ensembl:ENSG00000156875,Ensembl:ENSG00000283761 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006926876 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42773 RMVar_ID_42773 Human_SNP_ID_24947341 A-to-I Human chr1 + 100075912 100075911 100075912 GTTGTCCAGGCTGGTCTCAAACTCCTGGGTTCAAGCAGTCCTTCCATCTCAGTTCCCCAAAGTGC GTTGTCCAGGCTGGTCTCAAACTCCTGGGTTC_AGCAGTCCTTCCATCTCAGTTCCCCAAAGTGC CA C MFSD14A,AC118553.2 Ensembl:ENSG00000156875,Ensembl:ENSG00000283761 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1156472305 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_310522,RMVar_hsa_circ_332601,RMVar_hsa_circ_93532,RMVar_hsa_circ_134899,RMVar_hsa_circ_293291,RMVar_hsa_circ_300274,RMVar_hsa_circ_115531,RMVar_hsa_circ_134902,RMVar_hsa_circ_30827,RMVar_hsa_circ_134903,RMVar_hsa_circ_134907,RMVar_hsa_circ_121018,RMVar_hsa_circ_24954,RMVar_hsa_circ_63544 42774 RMVar_ID_42774 Human_SNP_ID_24950398 A-to-I Human chr1 - 100088419 100088419 100088419 AGACTTCGTGGCGTGTACCTGTAGTCTCAGCTAGTTGGAAGGATGAGGTGGGAGGATCGCTTGAG AGACTTCGTGGCGTGTACCTGTAGTCTCAGCTGGTTGGAAGGATGAGGTGGGAGGATCGCTTGAG T C SASS6 Ensembl:ENSG00000156876 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs541122231 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10489263,Human_RBP_ID_24564894 RMVar_hsa_circ_65282,RMVar_hsa_circ_134909,RMVar_hsa_circ_342389,RMVar_hsa_circ_372279 42775 RMVar_ID_42775 Human_SNP_ID_24951656 A-to-I Human chr1 - 100093504 100093504 100093504 TGCCTGCCTTGGCCTCCCAAAGTGTGGGGATTACAGGCATGAGCCACCACGCCCAGCCCTATTCT TGCCTGCCTTGGCCTCCCAAAGTGTGGGGATTGCAGGCATGAGCCACCACGCCCAGCCCTATTCT T C SASS6 Ensembl:ENSG00000156876 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1011300185 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24564966 RMVar_hsa_circ_65282,RMVar_hsa_circ_134909,RMVar_hsa_circ_342389,RMVar_hsa_circ_372279 42776 RMVar_ID_42776 Human_SNP_ID_24951678 A-to-I Human chr1 - 100093605 100093605 100093605 GGTGCACACCACCACACCTGCCTAATTTTCGTATTTTTTTGTAGAGACAGGGTTTTGCCATGTTT GGTGCACACCACCACACCTGCCTAATTTTCGTTTTTTTTTGTAGAGACAGGGTTTTGCCATGTTT T A SASS6 Ensembl:ENSG00000156876 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs906657999 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_65282,RMVar_hsa_circ_134909,RMVar_hsa_circ_342389,RMVar_hsa_circ_372279 42777 RMVar_ID_42777 Human_SNP_ID_24951679 A-to-I Human chr1 - 100093605 100093605 100093605 GGTGCACACCACCACACCTGCCTAATTTTCGTATTTTTTTGTAGAGACAGGGTTTTGCCATGTTT GGTGCACACCACCACACCTGCCTAATTTTCGTGTTTTTTTGTAGAGACAGGGTTTTGCCATGTTT T C SASS6 Ensembl:ENSG00000156876 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs906657999 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_65282,RMVar_hsa_circ_134909,RMVar_hsa_circ_342389,RMVar_hsa_circ_372279 42778 RMVar_ID_42778 Human_SNP_ID_24954050 A-to-I Human chr1 - 100104535 100104535 100104535 GAACTGCTTGAACCCAGGAGGTGGAGGTTGCCATGAGCCAAGATCGCACCACTGTACTCCAGCCT GAACTGCTTGAACCCAGGAGGTGGAGGTTGCCGTGAGCCAAGATCGCACCACTGTACTCCAGCCT T C SASS6 Ensembl:ENSG00000156876 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1385782161 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3175,RMVar_hsa_circ_303110,RMVar_hsa_circ_65282,RMVar_hsa_circ_342389,RMVar_hsa_circ_333193,RMVar_hsa_circ_357337,RMVar_hsa_circ_70313,RMVar_hsa_circ_26151,RMVar_hsa_circ_134910,RMVar_hsa_circ_134911,RMVar_hsa_circ_134912 42779 RMVar_ID_42779 Human_SNP_ID_24959138 A-to-I Human chr1 - 100124519 100124519 100124519 CAAATTAGCTGAATGTGGTGGCACACTCCTGTAGTTCCATCTACTTGAGAGGCTGAGGTGGAAGG CAAATTAGCTGAATGTGGTGGCACACTCCTGTGGTTCCATCTACTTGAGAGGCTGAGGTGGAAGG T C SASS6 Ensembl:ENSG00000156876 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1228777121 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63556,RMVar_hsa_circ_134913,RMVar_hsa_circ_293601 42780 RMVar_ID_42780 Human_SNP_ID_24959424 A-to-I Human chr1 - 100125593 100125593 100125593 GATCTCGGCTCACTCACCTCCCGGGTTCAAACAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGG GATCTCGGCTCACTCACCTCCCGGGTTCAAACGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGG T C SASS6 Ensembl:ENSG00000156876 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1225934771 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24749450 RMVar_hsa_circ_63556,RMVar_hsa_circ_134913,RMVar_hsa_circ_293601 42781 RMVar_ID_42781 Human_SNP_ID_24959425 A-to-I Human chr1 - 100125593 100125593 100125593 GATCTCGGCTCACTCACCTCCCGGGTTCAAACAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGG GATCTCGGCTCACTCACCTCCCGGGTTCAAACCATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGG T G SASS6 Ensembl:ENSG00000156876 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1225934771 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24749450 RMVar_hsa_circ_63556,RMVar_hsa_circ_134913,RMVar_hsa_circ_293601 42782 RMVar_ID_42782 Human_SNP_ID_24963057 A-to-I Human chr1 + 100140013 100140013 100140013 AAAATTAAAGTAGCACAGCAAAGACGGAGTAGAAATTTAGCAGTTGGACAATTCTGATGGCAGCT AAAATTAAAGTAGCACAGCAAAGACGGAGTAGCAATTTAGCAGTTGGACAATTCTGATGGCAGCT A C TRMT13 Ensembl:ENSG00000122435 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1163667717 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94127,RMVar_hsa_circ_134916,RMVar_hsa_circ_335790,RMVar_hsa_circ_134914,RMVar_hsa_circ_315737,RMVar_hsa_circ_134917,RMVar_hsa_circ_55736,RMVar_hsa_circ_279908,RMVar_hsa_circ_134918 42783 RMVar_ID_42783 Human_SNP_ID_24965730 A-to-I Human chr1 + 100151860 100151860 100151860 TACTTCAGAGGCTGAGGTCGGATGATCTCTTGAGCCCAGGAGTTCAAGGCTACAGTGAGCTATGA TACTTCAGAGGCTGAGGTCGGATGATCTCTTGCGCCCAGGAGTTCAAGGCTACAGTGAGCTATGA A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs943459785 Functional Loss SNV dbSNP153 33..33 33 - - - 42784 RMVar_ID_42784 Human_SNP_ID_24966206 A-to-I Human chr1 + 100153799 100153799 100153799 GTTTTGTTTTTAAGAAATAGTCTCTGTTTCCCAAGCTGGAGTACAGTGGCGCAATCTTGGCTCAC GTTTTGTTTTTAAGAAATAGTCTCTGTTTCCCGAGCTGGAGTACAGTGGCGCAATCTTGGCTCAC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1287404331 Functional Loss SNV dbSNP153 33..33 33 - - - 42785 RMVar_ID_42785 Human_SNP_ID_24966228 A-to-I Human chr1 + 100153881 100153881 100153881 GGGCTCAAGCGATCCTCCAGCCTCAGCCTCCCAAGTAGCTGTTATAGGCATGCACCACCACTCCC GGGCTCAAGCGATCCTCCAGCCTCAGCCTCCCTAGTAGCTGTTATAGGCATGCACCACCACTCCC A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1222860458 Functional Loss SNV dbSNP153 33..33 33 - - - 42786 RMVar_ID_42786 Human_SNP_ID_24977994 A-to-I Human chr1 - 100207033 100207033 100207033 ACTCTGTCTCCCAGGCTGGAGTGCAGTGGCACAATCTCGGCCCACTGCAACCTCCACCTCCCAGG ACTCTGTCTCCCAGGCTGGAGTGCAGTGGCACGATCTCGGCCCACTGCAACCTCCACCTCCCAGG T C DBT Ensembl:ENSG00000137992 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1395053390 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12161,RMVar_hsa_circ_32764,RMVar_hsa_circ_134929,RMVar_hsa_circ_295112,RMVar_hsa_circ_378510,RMVar_hsa_circ_134930,RMVar_hsa_circ_134931 42787 RMVar_ID_42787 Human_SNP_ID_24978713 A-to-I Human chr1 - 100210090 100210090 100210090 CCCAGGCTGGTCTTGAACTTCTGGTCTAAGCAATCCTCCTGCCTCAGCCTCCCAAAGTGCTGGGA CCCAGGCTGGTCTTGAACTTCTGGTCTAAGCAGTCCTCCTGCCTCAGCCTCCCAAAGTGCTGGGA T C DBT Ensembl:ENSG00000137992 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1176599207 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12161,RMVar_hsa_circ_32764,RMVar_hsa_circ_134929,RMVar_hsa_circ_295112,RMVar_hsa_circ_378510,RMVar_hsa_circ_134930,RMVar_hsa_circ_134931 42788 RMVar_ID_42788 Human_SNP_ID_24978738 A-to-I Human chr1 - 100210224 100210224 100210224 TCACTGCAGCCTCAACCTCTCAGGCCCAAGCAATCCTTCTGCCCCAGCCTCCTGTGTAGCTGGGA TCACTGCAGCCTCAACCTCTCAGGCCCAAGCAGTCCTTCTGCCCCAGCCTCCTGTGTAGCTGGGA T C DBT Ensembl:ENSG00000137992 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs952724784 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12161,RMVar_hsa_circ_32764,RMVar_hsa_circ_134929,RMVar_hsa_circ_295112,RMVar_hsa_circ_378510,RMVar_hsa_circ_134930,RMVar_hsa_circ_134931 42789 RMVar_ID_42789 Human_SNP_ID_24995661 A-to-I Human chr1 + 100283011 100283011 100283011 TAGAGACAGAGTTTCACCATGTTGGCCAGGCTAGTCTTGAACTCCTGTACTCAAGCTATCTGCCT TAGAGACAGAGTTTCACCATGTTGGCCAGGCTCGTCTTGAACTCCTGTACTCAAGCTATCTGCCT A C RTCA Ensembl:ENSG00000137996 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs763872416 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10491939 RMVar_hsa_circ_372469,RMVar_hsa_circ_134943,RMVar_hsa_circ_74230,RMVar_hsa_circ_267699 42790 RMVar_ID_42790 Human_SNP_ID_24996104 A-to-I Human chr1 + 100284633 100284633 100284633 CCAGGCTGGCCTCAAACTCCTGACCTCAAGTGATCCATCCGCCTCAGCCTCCCAAAGCATTGGGA CCAGGCTGGCCTCAAACTCCTGACCTCAAGTGGTCCATCCGCCTCAGCCTCCCAAAGCATTGGGA A G RTCA Ensembl:ENSG00000137996 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs929767902 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_372469,RMVar_hsa_circ_134943,RMVar_hsa_circ_74230,RMVar_hsa_circ_267699 42791 RMVar_ID_42791 Human_SNP_ID_24996105 A-to-I Human chr1 + 100284633 100284633 100284633 CCAGGCTGGCCTCAAACTCCTGACCTCAAGTGATCCATCCGCCTCAGCCTCCCAAAGCATTGGGA CCAGGCTGGCCTCAAACTCCTGACCTCAAGTGTTCCATCCGCCTCAGCCTCCCAAAGCATTGGGA A T RTCA Ensembl:ENSG00000137996 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs929767902 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_372469,RMVar_hsa_circ_134943,RMVar_hsa_circ_74230,RMVar_hsa_circ_267699 42792 RMVar_ID_42792 Human_SNP_ID_24996383 A-to-I Human chr1 + 100285674 100285673 100285675 TCAACAACAATTTTTTTTTTTTTGGTGGAGACAGAGTCTTGCTATGTTGCCCAGGCTGGTCTCGA TCAACAACAATTTTTTTTTTTTTGGTGGAGAC__AGTCTTGCTATGTTGCCCAGGCTGGTCTCGA CAG C RTCA Ensembl:ENSG00000137996 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1162947919 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_372469,RMVar_hsa_circ_134943,RMVar_hsa_circ_74230,RMVar_hsa_circ_298637,RMVar_hsa_circ_134946 42793 RMVar_ID_42793 Human_SNP_ID_24999057 A-to-I Human chr1 + 100296261 100296261 100296261 CAGGTGATTTCTCCCGCCTCAGTCTCCTGAGTAGCTAGGACTACAGGCACATGCCACCACGCCCA CAGGTGATTTCTCCCGCCTCAGTCTCCTGAGTGGCTAGGACTACAGGCACATGCCACCACGCCCA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs969642714 Functional Loss SNV dbSNP153 33..33 33 - - - 42794 RMVar_ID_42794 Human_SNP_ID_25025111 A-to-I Human chr1 + 100410091 100410091 100410091 AGAATTAACCAGGTGTGGTGGTGCATATCTGTAGTCTCAGCTACTTGGGAGGCTGAGGCAAGAGG AGAATTAACCAGGTGTGGTGGTGCATATCTGTGGTCTCAGCTACTTGGGAGGCTGAGGCAAGAGG A G CDC14A Ensembl:ENSG00000079335 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs963774738 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24749505 RMVar_hsa_circ_16584,RMVar_hsa_circ_41338,RMVar_hsa_circ_35105,RMVar_hsa_circ_368879,RMVar_hsa_circ_17419,RMVar_hsa_circ_283679,RMVar_hsa_circ_333114,RMVar_hsa_circ_352633,RMVar_hsa_circ_115381,RMVar_hsa_circ_134949 42795 RMVar_ID_42795 Human_SNP_ID_25152829 A-to-I Human chr1 + 100923656 100923656 100923656 AAAAATTAGCTGGGCATGGTGGTTGTGTACCTATAGTTGCAGCTACTTGGGATGCTGAGGCCGGA AAAAATTAGCTGGGCATGGTGGTTGTGTACCTGTAGTTGCAGCTACTTGGGATGCTGAGGCCGGA A G SLC30A7 Ensembl:ENSG00000162695 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs575830035 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10493525 RMVar_hsa_circ_103991,RMVar_hsa_circ_270118,RMVar_hsa_circ_15883,RMVar_hsa_circ_375314,RMVar_hsa_circ_335517,RMVar_hsa_circ_134970,RMVar_hsa_circ_96536,RMVar_hsa_circ_134972,RMVar_hsa_circ_134971,RMVar_hsa_circ_134969,RMVar_hsa_circ_315655,RMVar_hsa_circ_280969,RMVar_hsa_circ_134983,RMVar_hsa_circ_4239,RMVar_hsa_circ_134989 42796 RMVar_ID_42796 Human_SNP_ID_25152830 A-to-I Human chr1 + 100923658 100923658 100923658 AAATTAGCTGGGCATGGTGGTTGTGTACCTATAGTTGCAGCTACTTGGGATGCTGAGGCCGGAGG AAATTAGCTGGGCATGGTGGTTGTGTACCTATGGTTGCAGCTACTTGGGATGCTGAGGCCGGAGG A G SLC30A7 Ensembl:ENSG00000162695 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1218937357 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10493525 RMVar_hsa_circ_103991,RMVar_hsa_circ_270118,RMVar_hsa_circ_15883,RMVar_hsa_circ_375314,RMVar_hsa_circ_335517,RMVar_hsa_circ_134970,RMVar_hsa_circ_96536,RMVar_hsa_circ_134972,RMVar_hsa_circ_134971,RMVar_hsa_circ_134969,RMVar_hsa_circ_315655,RMVar_hsa_circ_280969,RMVar_hsa_circ_134983,RMVar_hsa_circ_4239,RMVar_hsa_circ_134989 42797 RMVar_ID_42797 Human_SNP_ID_25173344 A-to-I Human chr1 - 101016584 101016584 101016584 AAAATTAGCTGGGCGTGGTGGCGGGTGCCTGTAATCCCAGCTACCCGAGAGGCTGAGGGAGGGAC AAAATTAGCTGGGCGTGGTGGCGGGTGCCTGTTATCCCAGCTACCCGAGAGGCTGAGGGAGGGAC T A DPH5 Ensembl:ENSG00000117543 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1242351977 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_71565,RMVar_hsa_circ_134993,RMVar_hsa_circ_345333,RMVar_hsa_circ_280935,RMVar_hsa_circ_288911,RMVar_hsa_circ_55464 42798 RMVar_ID_42798 Human_SNP_ID_25183048 A-to-I Human chr1 + 101061607 101061607 101061607 AGGGGTAACACTATGTTGCCTCGACTGGTCTCAAACTCCTGGCCTCAAGCAGTCCTCCTGCCTAG AGGGGTAACACTATGTTGCCTCGACTGGTCTCCAACTCCTGGCCTCAAGCAGTCCTCCTGCCTAG A C AC093157.1 Ensembl:ENSG00000233184 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973719821 Functional Loss SNV dbSNP153 33..33 33 - - - 42799 RMVar_ID_42799 Human_SNP_ID_25394926 A-to-I Human chr1 + 101893609 101893609 101893609 GTTTTTACTTGACAAAGAAAAGACCTTTTCATATGTATGGATATACAGCTGGTTGTAGTATTGCA GTTTTTACTTGACAAAGAAAAGACCTTTTCATGTGTATGGATATACAGCTGGTTGTAGTATTGCA A G DNAJA1P5 Ensembl:ENSG00000162699 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs936121731 Functional Loss SNV dbSNP153 33..33 33 - - - 42800 RMVar_ID_42800 Human_SNP_ID_25417139 A-to-I Human chr1 - 101984057 101984057 101984057 TTTTGTAGAGCTGCGGTTTTGCCATGTTGCCCAGGCTGGCCTCAACTCCTGACCTCAAGTGATCT TTTTGTAGAGCTGCGGTTTTGCCATGTTGCCCGGGCTGGCCTCAACTCCTGACCTCAAGTGATCT T C OLFM3 Ensembl:ENSG00000118733 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs951972093 Functional Loss SNV dbSNP153 33..33 33 - - - 42801 RMVar_ID_42801 Human_SNP_ID_25417154 A-to-I Human chr1 - 101984118 101984118 101984118 TCTGGGCCTCAGCCTCCCAAGTAGCTGGCATTACAAGTGTGTGGCACCACGCTCAGCTAATTTTT TCTGGGCCTCAGCCTCCCAAGTAGCTGGCATTGCAAGTGTGTGGCACCACGCTCAGCTAATTTTT T C OLFM3 Ensembl:ENSG00000118733 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1352532314 Functional Loss SNV dbSNP153 33..33 33 - - - 42802 RMVar_ID_42802 Human_SNP_ID_25656865 A-to-I Human chr1 - 102905260 102905260 102905260 CACCCAGTAACTCGTCATTTAGCATTAGGTATATCTCCTAATGCTATCCCTCCCCCCTCCCCCCA CACCCAGTAACTCGTCATTTAGCATTAGGTATTTCTCCTAATGCTATCCCTCCCCCCTCCCCCCA T A COL11A1 Ensembl:ENSG00000060718 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs537520444 Functional Loss SNV dbSNP153 33..33 33 - - - 42803 RMVar_ID_42803 Human_SNP_ID_25656866 A-to-I Human chr1 - 102905260 102905260 102905260 CACCCAGTAACTCGTCATTTAGCATTAGGTATATCTCCTAATGCTATCCCTCCCCCCTCCCCCCA CACCCAGTAACTCGTCATTTAGCATTAGGTATCTCTCCTAATGCTATCCCTCCCCCCTCCCCCCA T G COL11A1 Ensembl:ENSG00000060718 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs537520444 Functional Loss SNV dbSNP153 33..33 33 - - - 42804 RMVar_ID_42804 Human_SNP_ID_11637313 A-to-I Human chr1 - 45017468 45017468 45017468 TGTGTCAGTTCTATGGCTGTGTACCTGTTTGAATATGTGCACACTGGACTGTGAGTTTCTACGTG TGTGTCAGTTCTATGGCTGTGTACCTGTTTGAGTATGTGCACACTGGACTGTGAGTTTCTACGTG T C ZSWIM5 Ensembl:ENSG00000162415 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs531377323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8312602,Human_RBP_ID_23398165 42805 RMVar_ID_42805 Human_SNP_ID_11639820 A-to-I Human chr1 - 45028721 45028721 45028721 AGACAGAGTCTCGCTCTGTCACCCAGGCTGAAATGAGTGGCGCGATTTCAGCTCACTGCAACCCC AGACAGAGTCTCGCTCTGTCACCCAGGCTGAAGTGAGTGGCGCGATTTCAGCTCACTGCAACCCC T C ZSWIM5 Ensembl:ENSG00000162415 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs367793864 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23578,RMVar_hsa_circ_339934 42806 RMVar_ID_42806 Human_SNP_ID_11644972 A-to-I Human chr1 + 45050208 45050208 45050208 AAAACCCCATCTCTACTAAAAATACAAAAATTAGCCGGGCGTGGTGGCTCTCACACCTGAAATCC AAAACCCCATCTCTACTAAAAATACAAAAATTTGCCGGGCGTGGTGGCTCTCACACCTGAAATCC A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1166818356 Functional Loss SNV dbSNP153 33..33 33 - - - 42807 RMVar_ID_42807 Human_SNP_ID_11665548 A-to-I Human chr1 - 45141960 45141960 45141960 AAACAATACACCCACCTCTCATATAGTAATATAAGACAAAGCAGACTTTGAACACACAAAAAACA AAACAATACACCCACCTCTCATATAGTAATATGAGACAAAGCAGACTTTGAACACACAAAAAACA T C ZSWIM5 Ensembl:ENSG00000162415 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1263731038 Functional Loss SNV dbSNP153 33..33 33 - - - 42808 RMVar_ID_42808 Human_SNP_ID_11665549 A-to-I Human chr1 - 45141968 45141968 45141968 CTAGGCTCAAACAATACACCCACCTCTCATATAGTAATATAAGACAAAGCAGACTTTGAACACAC CTAGGCTCAAACAATACACCCACCTCTCATATGGTAATATAAGACAAAGCAGACTTTGAACACAC T C ZSWIM5 Ensembl:ENSG00000162415 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs372791182 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5156886 42809 RMVar_ID_42809 Human_SNP_ID_11694401 A-to-I Human chr1 - 45269236 45269236 45269236 TTACTAAAAATACAAAAAAAAATTAGCTGGGTATGGTGGCGGGTGTCTGTAATCCCAGCTATTCG TTACTAAAAATACAAAAAAAAATTAGCTGGGTGTGGTGGCGGGTGTCTGTAATCCCAGCTATTCG T C ZSWIM5 Ensembl:ENSG00000162415 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1381879384 Functional Loss SNV dbSNP153 33..33 33 - - - 42810 RMVar_ID_42810 Human_SNP_ID_11702507 A-to-I Human chr1 - 45302766 45302766 45302766 TCGGCTAATTGCATCCTCCGCCTCCGGGGTTCAAGTGATTCTCCTGCCTCAGCTTCCAGAATAGC TCGGCTAATTGCATCCTCCGCCTCCGGGGTTCGAGTGATTCTCCTGCCTCAGCTTCCAGAATAGC T C ZSWIM5 Ensembl:ENSG00000162415 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1286681550 Functional Loss SNV dbSNP153 33..33 33 - - - 42811 RMVar_ID_42811 Human_SNP_ID_11703169 A-to-I Human chr1 + 45305110 45305110 45305110 CCTGTTCATCATGAGCAGAGGGGTGACTGAATAGAATGGGAGGCAGGTGTGGCCTGAGCAGTTCC CCTGTTCATCATGAGCAGAGGGGTGACTGAATGGAATGGGAGGCAGGTGTGGCCTGAGCAGTTCC A G LINC01144 Ensembl:ENSG00000281912 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1229005822 Functional Loss SNV dbSNP153 33..33 33 - - - 42812 RMVar_ID_42812 Human_SNP_ID_11753640 A-to-I Human chr1 + 45509578 45509577 45509578 GGGATGACAGGTGCCTGCCACTACACCTGGCTAATTTTTTGTATTTTTAGTAGAGATGGGGTTTC GGGATGACAGGTGCCTGCCACTACACCTGGCT_ATTTTTTGTATTTTTAGTAGAGATGGGGTTTC TA T MMACHC Ensembl:ENSG00000132763 Protein coding 3'UTR GSE100210;GSE99789 HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 29129909,29796672 RNA-Seq:(High) rs1303020618 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_96947 RMVar_hsa_circ_267386,RMVar_hsa_circ_110548,RMVar_hsa_circ_132503 42813 RMVar_ID_42813 Human_SNP_ID_11753648 A-to-I Human chr1 + 45509597 45509597 45509597 ACTACACCTGGCTAATTTTTTGTATTTTTAGTAGAGATGGGGTTTCATCATATTGGCCAGGCTGG ACTACACCTGGCTAATTTTTTGTATTTTTAGTGGAGATGGGGTTTCATCATATTGGCCAGGCTGG A G MMACHC Ensembl:ENSG00000132763 Protein coding 3'UTR GSE107867;GSE123020:GSM3490829,GSM3490830,GSM3490831 ASD brains,temporal_cortex;esophageal squamous carcinoma cells,EC109 cell line - 30559470,32596459 RNA-Seq:(High) rs1047690865 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267386,RMVar_hsa_circ_110548,RMVar_hsa_circ_132503 42814 RMVar_ID_42814 Human_SNP_ID_11753738 A-to-I Human chr1 + 45509924 45509924 45509924 ATACAGTGAAACCCCGTCTCTACTAAAAATGCAAAGTTAGCCGGGCATGGTAGCGCAGGCCTGTA ATACAGTGAAACCCCGTCTCTACTAAAAATGCCAAGTTAGCCGGGCATGGTAGCGCAGGCCTGTA A C MMACHC Ensembl:ENSG00000132763 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs987201507 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23149716 RMVar_hsa_circ_267386,RMVar_hsa_circ_110548,RMVar_hsa_circ_132503 42815 RMVar_ID_42815 Human_SNP_ID_11753751 A-to-I Human chr1 + 45509966 45509966 45509966 GGGCATGGTAGCGCAGGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGTAGAATCATTTGAA GGGCATGGTAGCGCAGGCCTGTAGTCCCAGCTGCTCAGGAGGCTGAGGCAGTAGAATCATTTGAA A G MMACHC Ensembl:ENSG00000132763 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs537216133 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267386,RMVar_hsa_circ_110548,RMVar_hsa_circ_132503 42816 RMVar_ID_42816 Human_SNP_ID_11753752 A-to-I Human chr1 + 45509966 45509966 45509966 GGGCATGGTAGCGCAGGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGTAGAATCATTTGAA GGGCATGGTAGCGCAGGCCTGTAGTCCCAGCTTCTCAGGAGGCTGAGGCAGTAGAATCATTTGAA A T MMACHC Ensembl:ENSG00000132763 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs537216133 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267386,RMVar_hsa_circ_110548,RMVar_hsa_circ_132503 42817 RMVar_ID_42817 Human_SNP_ID_11753764 A-to-I Human chr1 + 45510001 45510001 45510001 CAGGAGGCTGAGGCAGTAGAATCATTTGAACCAGGGAGGCAGAGATTGCAGTGAGCCGAGATTGC CAGGAGGCTGAGGCAGTAGAATCATTTGAACCGGGGAGGCAGAGATTGCAGTGAGCCGAGATTGC A G MMACHC Ensembl:ENSG00000132763 Protein coding 3'UTR GSE38233;GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,32596459 RNA-Seq:(High) rs1321448628 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26380795 Human_Splice_Rec_63956 RMVar_hsa_circ_267386,RMVar_hsa_circ_110548,RMVar_hsa_circ_132503 42818 RMVar_ID_42818 Human_SNP_ID_11753765 A-to-I Human chr1 + 45510009 45510008 45510010 TGAGGCAGTAGAATCATTTGAACCAGGGAGGCAGAGATTGCAGTGAGCCGAGATTGCATGGCTGC TGAGGCAGTAGAATCATTTGAACCAGGGAGGC__AGATTGCAGTGAGCCGAGATTGCATGGCTGC CAG C MMACHC Ensembl:ENSG00000132763 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs747970780 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_26386031 Human_Splice_Rec_63956 RMVar_hsa_circ_267386,RMVar_hsa_circ_110548,RMVar_hsa_circ_132503 42819 RMVar_ID_42819 Human_SNP_ID_11753785 A-to-I Human chr1 + 45510059 45510059 45510059 AGATTGCATGGCTGCACTCTAGCCTGGGTGACAGTGTGAGACTCTGTCTCAAAAAAAAAAAAAAA AGATTGCATGGCTGCACTCTAGCCTGGGTGACCGTGTGAGACTCTGTCTCAAAAAAAAAAAAAAA A C MMACHC Ensembl:ENSG00000132763 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1227994109 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26380796 Human_Splice_Rec_63956 Human_miRNA_ID_2449349 RMVar_hsa_circ_267386,RMVar_hsa_circ_110548,RMVar_hsa_circ_132503 42820 RMVar_ID_42820 Human_SNP_ID_11753955 A-to-I Human chr1 + 45510548 45510548 45510548 GACACTAAAAAAGACTATCTCTAATCAAGGCTAGAACCAAGGGAAGGCTAAGAATTGCCCAGTAC GACACTAAAAAAGACTATCTCTAATCAAGGCTGGAACCAAGGGAAGGCTAAGAATTGCCCAGTAC A G MMACHC Ensembl:ENSG00000132763 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1044711 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3314521,Human_RBP_ID_5830489,Human_RBP_ID_17218818,Human_RBP_ID_17336023,Human_RBP_ID_17453328,Human_RBP_ID_26380800,Human_RBP_ID_27595210 RMVar_hsa_circ_267386,RMVar_hsa_circ_110548,RMVar_hsa_circ_132503 42821 RMVar_ID_42821 Human_SNP_ID_11754488 A-to-I Human chr1 - 45512370 45512370 45512370 ACCACCACGCCCCACTATTTTTGTATAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCA ACCACCACGCCCCACTATTTTTGTATAGTCCCGGCTACTCGGGAGGCTGAGGCAGGAGAATGGCA T C PRDX1 Ensembl:ENSG00000117450 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1375619831 Functional Loss SNV dbSNP153 33..33 33 - - - 42822 RMVar_ID_42822 Human_SNP_ID_11756705 A-to-I Human chr1 - 45520153 45520153 45520153 TTGCCCAGGCTGGAGTGCAGTGGCGCGATCTCAGCTTACTGCAACCTCTGCCTCCCGGGTTCAAG TTGCCCAGGCTGGAGTGCAGTGGCGCGATCTCGGCTTACTGCAACCTCTGCCTCCCGGGTTCAAG T C PRDX1 Ensembl:ENSG00000117450 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs927857988 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89722,RMVar_hsa_circ_132504 42823 RMVar_ID_42823 Human_SNP_ID_11756706 A-to-I Human chr1 - 45520153 45520153 45520153 TTGCCCAGGCTGGAGTGCAGTGGCGCGATCTCAGCTTACTGCAACCTCTGCCTCCCGGGTTCAAG TTGCCCAGGCTGGAGTGCAGTGGCGCGATCTCCGCTTACTGCAACCTCTGCCTCCCGGGTTCAAG T G PRDX1 Ensembl:ENSG00000117450 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs927857988 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89722,RMVar_hsa_circ_132504 42824 RMVar_ID_42824 Human_SNP_ID_11765690 A-to-I Human chr1 + 45554060 45554060 45554060 GTGGTGGCTCACACCTGTAATCCCAGCACTTTAGGAGGCCAAGGTGGGAGGGTCACTTGAGGCTA GTGGTGGCTCACACCTGTAATCCCAGCACTTTTGGAGGCCAAGGTGGGAGGGTCACTTGAGGCTA A T AKR1A1 Ensembl:ENSG00000117448 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs768630374 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_341700,RMVar_hsa_circ_99348,RMVar_hsa_circ_132508,RMVar_hsa_circ_132509 42825 RMVar_ID_42825 Human_SNP_ID_11765707 A-to-I Human chr1 + 45554165 45554165 45554165 AAAGAAAAATAAGGCCAGGCATAGTGGCTCACACTTATAATCCCAGCACTTTGGGAGGCTGAGGC AAAGAAAAATAAGGCCAGGCATAGTGGCTCACCCTTATAATCCCAGCACTTTGGGAGGCTGAGGC A C AKR1A1 Ensembl:ENSG00000117448 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1453426271 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_341700,RMVar_hsa_circ_99348,RMVar_hsa_circ_132508,RMVar_hsa_circ_132509 42826 RMVar_ID_42826 Human_SNP_ID_11765823 A-to-I Human chr1 + 45554760 45554760 45554760 TGGCCCAAGCTGGAGTGCAGTGGTGTGATTTCAGCTCATTGCAACCTCTGCCCCCCAGGCTCAAG TGGCCCAAGCTGGAGTGCAGTGGTGTGATTTCTGCTCATTGCAACCTCTGCCCCCCAGGCTCAAG A T AKR1A1 Ensembl:ENSG00000117448 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1295420697 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_341700,RMVar_hsa_circ_99348,RMVar_hsa_circ_132508,RMVar_hsa_circ_132509 42827 RMVar_ID_42827 Human_SNP_ID_11765866 A-to-I Human chr1 + 45554943 45554943 45554943 GAACTCCTGGACTCAAGCAATCTGCTTGCCTCAGCCTCCCAAAGTGCTGGGATTAACAGGCATGA GAACTCCTGGACTCAAGCAATCTGCTTGCCTCGGCCTCCCAAAGTGCTGGGATTAACAGGCATGA A G AKR1A1 Ensembl:ENSG00000117448 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs57904478 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_341700,RMVar_hsa_circ_99348,RMVar_hsa_circ_132508,RMVar_hsa_circ_132509 42828 RMVar_ID_42828 Human_SNP_ID_11767269 A-to-I Human chr1 + 45560489 45560489 45560489 AAAAACATCCAGGTGTGCTGGCACAGGCCTGTAGTCCCAGCTACTTGGAAGGGTGAGGCAGGAAT AAAAACATCCAGGTGTGCTGGCACAGGCCTGTGGTCCCAGCTACTTGGAAGGGTGAGGCAGGAAT A G AKR1A1 Ensembl:ENSG00000117448 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1444027262 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_341700,RMVar_hsa_circ_99348,RMVar_hsa_circ_132508,RMVar_hsa_circ_132509 42829 RMVar_ID_42829 Human_SNP_ID_11769071 A-to-I Human chr1 + 45567639 45567639 45567639 CACGAGGTCAGGAGATCGAGATCATCCTGGCTAACACGGTGAAACCCCGTCTCTACTAAAAATAC CACGAGGTCAGGAGATCGAGATCATCCTGGCTGACACGGTGAAACCCCGTCTCTACTAAAAATAC A G AKR1A1 Ensembl:ENSG00000117448 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1557636752 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_96431 RMVar_hsa_circ_99348,RMVar_hsa_circ_77432,RMVar_hsa_circ_132510,RMVar_hsa_circ_132509,RMVar_hsa_circ_82270,RMVar_hsa_circ_113240,RMVar_hsa_circ_105747,RMVar_hsa_circ_132511,RMVar_hsa_circ_132513,RMVar_hsa_circ_132512,RMVar_hsa_circ_117148,RMVar_hsa_circ_132517 42830 RMVar_ID_42830 Human_SNP_ID_11769086 A-to-I Human chr1 + 45567674 45567674 45567674 ACGGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTAGCTGCGCGTGGTGGTGAGCGCCTGTA ACGGTGAAACCCCGTCTCTACTAAAAATACAACAAATTAGCTGCGCGTGGTGGTGAGCGCCTGTA A C AKR1A1 Ensembl:ENSG00000117448 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1274557224 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99348,RMVar_hsa_circ_77432,RMVar_hsa_circ_132510,RMVar_hsa_circ_132509,RMVar_hsa_circ_82270,RMVar_hsa_circ_113240,RMVar_hsa_circ_105747,RMVar_hsa_circ_132511,RMVar_hsa_circ_132513,RMVar_hsa_circ_132512,RMVar_hsa_circ_117148,RMVar_hsa_circ_132517 42831 RMVar_ID_42831 Human_SNP_ID_11769112 A-to-I Human chr1 + 45567752 45567752 45567752 GGGAGGCTGAGGCAGGAGAATGGCGTGAACCCAGGAGGTGGAGCTTGCAGTGAGCTGAGATAGTG GGGAGGCTGAGGCAGGAGAATGGCGTGAACCCGGGAGGTGGAGCTTGCAGTGAGCTGAGATAGTG A G AKR1A1 Ensembl:ENSG00000117448 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs550155592 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99348,RMVar_hsa_circ_77432,RMVar_hsa_circ_132510,RMVar_hsa_circ_132509,RMVar_hsa_circ_82270,RMVar_hsa_circ_113240,RMVar_hsa_circ_105747,RMVar_hsa_circ_132511,RMVar_hsa_circ_132513,RMVar_hsa_circ_132512,RMVar_hsa_circ_117148,RMVar_hsa_circ_132517 42832 RMVar_ID_42832 Human_SNP_ID_11769407 A-to-I Human chr1 + 45568603 45568603 45568603 GGGCTCCTCTGATCGTGCATGGCGTGATCCTGATGAGCCTGTCCTGCTGGAGGAACCAGTAGTCC GGGCTCCTCTGATCGTGCATGGCGTGATCCTGTTGAGCCTGTCCTGCTGGAGGAACCAGTAGTCC A T AKR1A1 Ensembl:ENSG00000117448 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417957195 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_356449,Human_RBP_ID_742227,Human_RBP_ID_4055870,Human_RBP_ID_22427239 Human_Splice_Rec_64013,Human_Splice_Rec_64031,Human_Splice_Rec_64077,Human_Splice_Rec_64111 Human_miRNA_ID_165463,Human_miRNA_ID_595660,Human_miRNA_ID_1997305,Human_miRNA_ID_2219317,Human_miRNA_ID_2482352,Human_miRNA_ID_2625309,Human_miRNA_ID_2746129,Human_miRNA_ID_3070729 RMVar_hsa_circ_99348,RMVar_hsa_circ_77432,RMVar_hsa_circ_132510,RMVar_hsa_circ_132509,RMVar_hsa_circ_82270,RMVar_hsa_circ_113240,RMVar_hsa_circ_132511,RMVar_hsa_circ_132512,RMVar_hsa_circ_117148,RMVar_hsa_circ_132517,RMVar_hsa_circ_124502,RMVar_hsa_circ_132520,RMVar_hsa_circ_92582,RMVar_hsa_circ_132521 42833 RMVar_ID_42833 Human_SNP_ID_11775104 A-to-I Human chr1 + 45588261 45588261 45588261 AAGTAGTTGGGATTACAGGCGCCCGCCACCACACCTGGCTAATTTTTGTATTTTTAGTAGAAATG AAGTAGTTGGGATTACAGGCGCCCGCCACCACCCCTGGCTAATTTTTGTATTTTTAGTAGAAATG A C NASP Ensembl:ENSG00000132780 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1312545074 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_348603 42834 RMVar_ID_42834 Human_SNP_ID_11775110 A-to-I Human chr1 + 45588301 45588301 45588301 AATTTTTGTATTTTTAGTAGAAATGAGGTTTTACCATGTTGGCCAGGCTGGTCTCGAACTCCTGA AATTTTTGTATTTTTAGTAGAAATGAGGTTTTGCCATGTTGGCCAGGCTGGTCTCGAACTCCTGA A G NASP Ensembl:ENSG00000132780 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1018468801 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_348603 42835 RMVar_ID_42835 Human_SNP_ID_11775580 A-to-I Human chr1 + 45589780 45589780 45589780 AAAATTAGCCAGGCGTGGTGGTGGGCGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGA AAAATTAGCCAGGCGTGGTGGTGGGCGCCTGTTATCCCAGCTACTTGGGAGGCTGAGGCAGGAGA A T NASP Ensembl:ENSG00000132780 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1977650 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_348603 42836 RMVar_ID_42836 Human_SNP_ID_11776454 A-to-I Human chr1 + 45592754 45592754 45592754 TCAGGCTGGTCTCGAACTCCTGACCTCGGGCGATCTGCCCGTCTTGGCCTCCCAGAGTGCTGGGA TCAGGCTGGTCTCGAACTCCTGACCTCGGGCGGTCTGCCCGTCTTGGCCTCCCAGAGTGCTGGGA A G NASP Ensembl:ENSG00000132780 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs548236444 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91567,RMVar_hsa_circ_318243,RMVar_hsa_circ_322904,RMVar_hsa_circ_317051,RMVar_hsa_circ_132525,RMVar_hsa_circ_63217,RMVar_hsa_circ_132526 42837 RMVar_ID_42837 Human_SNP_ID_11777025 A-to-I Human chr1 + 45594640 45594640 45594640 GTGATCCTCCTGCCTTAGACTCCTGGGTAGCTAGGATCACAGATGTGTGCCACTATGCCTGGCTA GTGATCCTCCTGCCTTAGACTCCTGGGTAGCTGGGATCACAGATGTGTGCCACTATGCCTGGCTA A G NASP Ensembl:ENSG00000132780 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs145890624 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91567,RMVar_hsa_circ_318243,RMVar_hsa_circ_322904,RMVar_hsa_circ_317051,RMVar_hsa_circ_132525,RMVar_hsa_circ_63217,RMVar_hsa_circ_132526 42838 RMVar_ID_42838 Human_SNP_ID_11780362 A-to-I Human chr1 - 45607047 45607047 45607047 TTACCAGTTAGGTAAGAGATGCCAAGCTTTTCATTCTCCCCCATCTGATATGTAAAACTATAGCA TTACCAGTTAGGTAAGAGATGCCAAGCTTTTCGTTCTCCCCCATCTGATATGTAAAACTATAGCA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs534785007 Functional Loss SNV dbSNP153 33..33 33 - - - 42839 RMVar_ID_42839 Human_SNP_ID_11781313 A-to-I Human chr1 + 45609929 45609929 45609929 ACTGCTTAGAAATTTTGTCGTGGGCTGGGCGCAGTAGCTTCACACCTGTATCCCAGCACTTTGAG ACTGCTTAGAAATTTTGTCGTGGGCTGGGCGCGGTAGCTTCACACCTGTATCCCAGCACTTTGAG A G NASP Ensembl:ENSG00000132780 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1301560689 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_221911,Human_RBP_ID_5830833,Human_RBP_ID_11007014,Human_RBP_ID_24702115 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 42840 RMVar_ID_42840 Human_SNP_ID_11781316 A-to-I Human chr1 + 45609940 45609940 45609940 ATTTTGTCGTGGGCTGGGCGCAGTAGCTTCACACCTGTATCCCAGCACTTTGAGAGGCCGAGGTG ATTTTGTCGTGGGCTGGGCGCAGTAGCTTCACGCCTGTATCCCAGCACTTTGAGAGGCCGAGGTG A G NASP Ensembl:ENSG00000132780 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1058883 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_221911,Human_RBP_ID_24702115 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 42841 RMVar_ID_42841 Human_SNP_ID_11781323 A-to-I Human chr1 + 45609976 45609976 45609976 GTATCCCAGCACTTTGAGAGGCCGAGGTGGGCAGATCACATGGTCAGAAGTTTGAGACCAGCCTG GTATCCCAGCACTTTGAGAGGCCGAGGTGGGCGGATCACATGGTCAGAAGTTTGAGACCAGCCTG A G NASP Ensembl:ENSG00000132780 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1208165836 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42842 RMVar_ID_42842 Human_SNP_ID_11781333 A-to-I Human chr1 + 45610048 45610048 45610048 TGTTGAAACTTTGACTCTACTAAAAATACAAAAATTAGCTGGACGTGGTGGCATGCGCCTGTGGT TGTTGAAACTTTGACTCTACTAAAAATACAAACATTAGCTGGACGTGGTGGCATGCGCCTGTGGT A C NASP Ensembl:ENSG00000132780 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs566335996 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557160 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 42843 RMVar_ID_42843 Human_SNP_ID_11781334 A-to-I Human chr1 + 45610048 45610048 45610048 TGTTGAAACTTTGACTCTACTAAAAATACAAAAATTAGCTGGACGTGGTGGCATGCGCCTGTGGT TGTTGAAACTTTGACTCTACTAAAAATACAAAGATTAGCTGGACGTGGTGGCATGCGCCTGTGGT A G NASP Ensembl:ENSG00000132780 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs566335996 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557160 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 42844 RMVar_ID_42844 Human_SNP_ID_11781542 A-to-I Human chr1 + 45610802 45610802 45610802 GCAGTGGTGCGGTCTCGCTCACTGCAACCTGCATCTCCCAGGTTCAAGCGATTCTCCTACGTCAG GCAGTGGTGCGGTCTCGCTCACTGCAACCTGCTTCTCCCAGGTTCAAGCGATTCTCCTACGTCAG A T NASP Ensembl:ENSG00000132780 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs932149425 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8312785 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 42845 RMVar_ID_42845 Human_SNP_ID_11781551 A-to-I Human chr1 + 45610828 45610828 45610828 ACCTGCATCTCCCAGGTTCAAGCGATTCTCCTACGTCAGCCTCCTGAGTAGCTGGGACTAAAGGC ACCTGCATCTCCCAGGTTCAAGCGATTCTCCTGCGTCAGCCTCCTGAGTAGCTGGGACTAAAGGC A G NASP Ensembl:ENSG00000132780 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 31158229,32596459 RNA-Seq:(High) rs1031664286 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11214627 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 42846 RMVar_ID_42846 Human_SNP_ID_11781566 A-to-I Human chr1 + 45610871 45610871 45610871 CTGAGTAGCTGGGACTAAAGGCACATGTCCCCAGGCCCGACTAATTTTTTTGTATTTTTACTAGA CTGAGTAGCTGGGACTAAAGGCACATGTCCCCGGGCCCGACTAATTTTTTTGTATTTTTACTAGA A G NASP Ensembl:ENSG00000132780 Protein coding intron GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831 HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line - 29129909,32596459 RNA-Seq:(High) rs564197667 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5830845 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 42847 RMVar_ID_42847 Human_SNP_ID_11781832 A-to-I Human chr1 + 45611673 45611673 45611673 TATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGGTCCCAATCTCCTGACCTGGTGA TATTTTTAGTAGAGACGGGGTTTCACCGTGTTGGCCAGGATGGTCCCAATCTCCTGACCTGGTGA A G NASP Ensembl:ENSG00000132780 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 31158229,32596459 RNA-Seq:(High) rs1034982494 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42848 RMVar_ID_42848 Human_SNP_ID_11781847 A-to-I Human chr1 + 45611734 45611734 45611734 GTGATCTGCCCACCTTGGCCTCCCAAAGTGCTAGGATTACAGGTGTGAGCCACCGCGCCTGGCAG GTGATCTGCCCACCTTGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCGCCTGGCAG A G NASP Ensembl:ENSG00000132780 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs544097665 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_96957 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 42849 RMVar_ID_42849 Human_SNP_ID_11783599 A-to-I Human chr1 - 45617581 45617581 45617581 TAAGCCCTGCTTAACTGCCCACCTCCTCCTCCATGTTTTCCGAAACTTCATTTCCACTGGGGACA TAAGCCCTGCTTAACTGCCCACCTCCTCCTCCGTGTTTTCCGAAACTTCATTTCCACTGGGGACA T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1553173715 Functional Loss SNV dbSNP153 33..33 33 - - - 42850 RMVar_ID_42850 Human_SNP_ID_11787361 A-to-I Human chr1 - 45627027 45627027 45627027 AGCTCACTGTAAGCTCCGCCTCCCGGGTTCCCACCATTCTCCTGCCTCAGCCTCCTGAGTAGCTG AGCTCACTGTAAGCTCCGCCTCCCGGGTTCCCGCCATTCTCCTGCCTCAGCCTCCTGAGTAGCTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs961784018 Functional Loss SNV dbSNP153 33..33 33 - - - 42851 RMVar_ID_42851 Human_SNP_ID_11788835 A-to-I Human chr1 - 45631391 45631391 45631391 GGGCATGGTAGCATGCACCCATAGTCACAGCTACATGGGAGGCTGAGGCATGAGAATCACTTGAA GGGCATGGTAGCATGCACCCATAGTCACAGCTGCATGGGAGGCTGAGGCATGAGAATCACTTGAA T C GPBP1L1 Ensembl:ENSG00000159592 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs959511577 Functional Loss SNV dbSNP153 33..33 33 - - - 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_132547,RMVar_hsa_circ_132548,RMVar_hsa_circ_132549,RMVar_hsa_circ_132546 42852 RMVar_ID_42852 Human_SNP_ID_11795607 A-to-I Human chr1 - 45655971 45655971 45655971 GGCCAGGACTGAGAGATCAGCCTGGGCAACATAGTGAGACCCCCATCTCTACAAAAAATTTAGAA GGCCAGGACTGAGAGATCAGCCTGGGCAACATGGTGAGACCCCCATCTCTACAAAAAATTTAGAA T C GPBP1L1 Ensembl:ENSG00000159592 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs932133868 Functional Loss SNV dbSNP153 33..33 33 - - - 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_343973,RMVar_hsa_circ_379075,RMVar_hsa_circ_132564 42853 RMVar_ID_42853 Human_SNP_ID_11795777 A-to-I Human chr1 - 45656670 45656670 45656670 CTGAGACCCTGGCTCTTAAAAAAAAAAAAAAAAGGCTTATGTATGTATTTTGTTGATTTTTGACT CTGAGACCCTGGCTCTTAAAAAAAAAAAAAAAGGGCTTATGTATGTATTTTGTTGATTTTTGACT T C GPBP1L1 Ensembl:ENSG00000159592 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1399547443 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24766262 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_343973,RMVar_hsa_circ_379075,RMVar_hsa_circ_132564 42854 RMVar_ID_42854 Human_SNP_ID_11795792 A-to-I Human chr1 - 45656731 45656731 45656731 AGCCAAGGAGTTTGAGGCTACAGTGAGCTGTGATCGGGCTACTGTACTCCAGCCTGGGTGACTGA AGCCAAGGAGTTTGAGGCTACAGTGAGCTGTGTTCGGGCTACTGTACTCCAGCCTGGGTGACTGA T A GPBP1L1 Ensembl:ENSG00000159592 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559475936 Functional Loss SNV dbSNP153 33..33 33 - - - 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_343973,RMVar_hsa_circ_379075,RMVar_hsa_circ_132564 42855 RMVar_ID_42855 Human_SNP_ID_11795793 A-to-I Human chr1 - 45656731 45656731 45656731 AGCCAAGGAGTTTGAGGCTACAGTGAGCTGTGATCGGGCTACTGTACTCCAGCCTGGGTGACTGA AGCCAAGGAGTTTGAGGCTACAGTGAGCTGTGGTCGGGCTACTGTACTCCAGCCTGGGTGACTGA T C GPBP1L1 Ensembl:ENSG00000159592 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559475936 Functional Loss SNV dbSNP153 33..33 33 - - - 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_343973,RMVar_hsa_circ_379075,RMVar_hsa_circ_132564 42856 RMVar_ID_42856 Human_SNP_ID_11795809 A-to-I Human chr1 - 45656794 45656794 45656794 AGGTGTGGTGGTGAATACCTGTCATCTCAGCTACTTGGGAGGCTAAGGCAGGAGGATTGCTTGAG AGGTGTGGTGGTGAATACCTGTCATCTCAGCTGCTTGGGAGGCTAAGGCAGGAGGATTGCTTGAG T C GPBP1L1 Ensembl:ENSG00000159592 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1217152319 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24766263 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_343973,RMVar_hsa_circ_379075,RMVar_hsa_circ_132564 42857 RMVar_ID_42857 Human_SNP_ID_11796037 A-to-I Human chr1 - 45657611 45657611 45657611 GGCCTCAAACGATCCTGTCACCTCAGCCTCCAAAAGTGCTGAGATTACAGGCATGAGCCACTGTA GGCCTCAAACGATCCTGTCACCTCAGCCTCCAGAAGTGCTGAGATTACAGGCATGAGCCACTGTA T C GPBP1L1 Ensembl:ENSG00000159592 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs745469125 Functional Loss SNV dbSNP153 33..33 33 - - - 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_343973,RMVar_hsa_circ_379075,RMVar_hsa_circ_132564 42858 RMVar_ID_42858 Human_SNP_ID_11796038 A-to-I Human chr1 - 45657611 45657611 45657611 GGCCTCAAACGATCCTGTCACCTCAGCCTCCAAAAGTGCTGAGATTACAGGCATGAGCCACTGTA GGCCTCAAACGATCCTGTCACCTCAGCCTCCACAAGTGCTGAGATTACAGGCATGAGCCACTGTA T G GPBP1L1 Ensembl:ENSG00000159592 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs745469125 Functional Loss SNV dbSNP153 33..33 33 - - - 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_343973,RMVar_hsa_circ_379075,RMVar_hsa_circ_132564 42859 RMVar_ID_42859 Human_SNP_ID_11796042 A-to-I Human chr1 - 45657619 45657619 45657619 CTAGAACTGGCCTCAAACGATCCTGTCACCTCAGCCTCCAAAAGTGCTGAGATTACAGGCATGAG CTAGAACTGGCCTCAAACGATCCTGTCACCTCGGCCTCCAAAAGTGCTGAGATTACAGGCATGAG T C GPBP1L1 Ensembl:ENSG00000159592 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1045433838 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11008015 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_343973,RMVar_hsa_circ_379075,RMVar_hsa_circ_132564 42860 RMVar_ID_42860 Human_SNP_ID_11797423 A-to-I Human chr1 - 45662968 45662968 45662968 CGGCTCACTGTAACCTCCGCCTCCCGGATTCAAGTTATTCTCTTGCCTCAGCCTCCTGAGTAGCT CGGCTCACTGTAACCTCCGCCTCCCGGATTCAGGTTATTCTCTTGCCTCAGCCTCCTGAGTAGCT T C GPBP1L1 Ensembl:ENSG00000159592 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1331531116 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80147,RMVar_hsa_circ_132562 42861 RMVar_ID_42861 Human_SNP_ID_11797878 A-to-I Human chr1 - 45664444 45664444 45664444 CTCCTGCCTCAGCCTCCGTAGTAGCTGGAACTACATGCGCCCACCACCACGCCCAGCTAATTTTT CTCCTGCCTCAGCCTCCGTAGTAGCTGGAACTTCATGCGCCCACCACCACGCCCAGCTAATTTTT T A GPBP1L1 Ensembl:ENSG00000159592 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1018538246 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80147,RMVar_hsa_circ_132562 42862 RMVar_ID_42862 Human_SNP_ID_11798026 A-to-I Human chr1 - 45664857 45664857 45664857 CTGGCTAACATGGCGAAACTCTATCTCTGCTAAAAATACAAAAATTAACCGGGTGTGGTGGTGGG CTGGCTAACATGGCGAAACTCTATCTCTGCTATAAATACAAAAATTAACCGGGTGTGGTGGTGGG T A GPBP1L1 Ensembl:ENSG00000159592 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1384113580 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80147,RMVar_hsa_circ_132562 42863 RMVar_ID_42863 Human_SNP_ID_11798138 A-to-I Human chr1 - 45665245 45665245 45665245 TTTTTCTTTGTGAGAGTCTCCCTCAGCCTGCAATGGCGTGATCTCGGCTCACTTCAACCTCCCGA TTTTTCTTTGTGAGAGTCTCCCTCAGCCTGCAGTGGCGTGATCTCGGCTCACTTCAACCTCCCGA T C GPBP1L1 Ensembl:ENSG00000159592 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1216471514 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80147,RMVar_hsa_circ_132562 42864 RMVar_ID_42864 Human_SNP_ID_11798186 A-to-I Human chr1 - 45665494 45665494 45665494 CGCCTGCCTCAGACTCTCAAAGTGCTGGGATTACAAGTGTGAGCCACCGCGCTTGGCCAACTTTT CGCCTGCCTCAGACTCTCAAAGTGCTGGGATTGCAAGTGTGAGCCACCGCGCTTGGCCAACTTTT T C GPBP1L1 Ensembl:ENSG00000159592 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs111408562 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80147,RMVar_hsa_circ_132562 42865 RMVar_ID_42865 Human_SNP_ID_11798209 A-to-I Human chr1 - 45665569 45665567 45665569 ACCCGGCTAGTTTTTGTATTTTTAGCAGAGACAGGGTTTCACCATGTTGGTCGGGCTGGTCTCGA ACCCGGCTAGTTTTTGTATTTTTAGCAGAGAC__GGTTTCACCATGTTGGTCGGGCTGGTCTCGA CCT C GPBP1L1 Ensembl:ENSG00000159592 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1343034608 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_80147,RMVar_hsa_circ_132562 42866 RMVar_ID_42866 Human_SNP_ID_11798211 A-to-I Human chr1 - 45665569 45665569 45665569 ACCCGGCTAGTTTTTGTATTTTTAGCAGAGACAGGGTTTCACCATGTTGGTCGGGCTGGTCTCGA ACCCGGCTAGTTTTTGTATTTTTAGCAGAGACGGGGTTTCACCATGTTGGTCGGGCTGGTCTCGA T C GPBP1L1 Ensembl:ENSG00000159592 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1403682402 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80147,RMVar_hsa_circ_132562 42867 RMVar_ID_42867 Human_SNP_ID_11803104 A-to-I Human chr1 - 45683908 45683904 45683908 TTTGTTTTGTTTTGTTTTTGATACGGGGTCTCACTCTGTCACCCAGATTGGAGTGCGGTGGCATG TTTGTTTTGTTTTGTTTTTGATACGGGGTCTC____TGTCACCCAGATTGGAGTGCGGTGGCATG AGAGT A GPBP1L1 Ensembl:ENSG00000159592 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1035769110 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_11008577,Human_RBP_ID_23398655 RMVar_hsa_circ_80147,RMVar_hsa_circ_132562 42868 RMVar_ID_42868 Human_SNP_ID_11806266 A-to-I Human chr1 - 45694982 45694982 45694982 TCTAGAGATGCTGAGGCAGGAGAATCGCTTGAACTCGGGAGGTGGAGGTTGCGGTGAGCCAAGAT TCTAGAGATGCTGAGGCAGGAGAATCGCTTGATCTCGGGAGGTGGAGGTTGCGGTGAGCCAAGAT T A AL604028.1,IPP Ensembl:ENSG00000230896,Ensembl:ENSG00000197429 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1464300730 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8243631 42869 RMVar_ID_42869 Human_SNP_ID_11806273 A-to-I Human chr1 - 45695011 45695011 45695011 TGGTGGCACGTGCCTATAATCCCAGCTACTCTAGAGATGCTGAGGCAGGAGAATCGCTTGAACTC TGGTGGCACGTGCCTATAATCCCAGCTACTCTGGAGATGCTGAGGCAGGAGAATCGCTTGAACTC T C AL604028.1,IPP Ensembl:ENSG00000230896,Ensembl:ENSG00000197429 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1239543990 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8243631 42870 RMVar_ID_42870 Human_SNP_ID_11806278 A-to-I Human chr1 - 45695028 45695028 45695028 AAAAAATTAGTTGGGCATGGTGGCACGTGCCTATAATCCCAGCTACTCTAGAGATGCTGAGGCAG AAAAAATTAGTTGGGCATGGTGGCACGTGCCTGTAATCCCAGCTACTCTAGAGATGCTGAGGCAG T C AL604028.1,IPP Ensembl:ENSG00000230896,Ensembl:ENSG00000197429 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1055132234 Functional Loss SNV dbSNP153 33..33 33 - - - 42871 RMVar_ID_42871 Human_SNP_ID_11806378 A-to-I Human chr1 - 45695434 45695434 45695434 CTTCTGCACTGGGTGCAGTGGCTCACGCCTGCAATCCTAACACTTTGGGAGCCTAGGCAGGAGGA CTTCTGCACTGGGTGCAGTGGCTCACGCCTGCTATCCTAACACTTTGGGAGCCTAGGCAGGAGGA T A AL604028.1,IPP Ensembl:ENSG00000230896,Ensembl:ENSG00000197429 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1327550537 Functional Loss SNV dbSNP153 33..33 33 - - - 42872 RMVar_ID_42872 Human_SNP_ID_11806479 A-to-I Human chr1 - 45695775 45695775 45695775 ATCCCAGGTACTCGGGAGGCTGAGGCAGGAGAATCGCTTCAACACGGGAGGCGGAGGTTGCGGTG ATCCCAGGTACTCGGGAGGCTGAGGCAGGAGAGTCGCTTCAACACGGGAGGCGGAGGTTGCGGTG T C AL604028.1,IPP Ensembl:ENSG00000230896,Ensembl:ENSG00000197429 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1325255592 Functional Loss SNV dbSNP153 33..33 33 - - - 42873 RMVar_ID_42873 Human_SNP_ID_11806696 A-to-I Human chr1 - 45696613 45696613 45696613 ACGAGGCCCAGCTAATTTTGTATTTTTTGTAGAGGTGGGGTTTCTCCATCTTGGTCACGCTTGAC ACGAGGCCCAGCTAATTTTGTATTTTTTGTAGCGGTGGGGTTTCTCCATCTTGGTCACGCTTGAC T G AL604028.1,IPP Ensembl:ENSG00000230896,Ensembl:ENSG00000197429 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs544440593 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_356613 42874 RMVar_ID_42874 Human_SNP_ID_11806729 A-to-I Human chr1 - 45696717 45696717 45696717 GGAGTGCAATAGCATGATCTTGGCTCACCGCAACCTTTGCCGCCCGGGTTCAAGCGATTCTCCCG GGAGTGCAATAGCATGATCTTGGCTCACCGCAGCCTTTGCCGCCCGGGTTCAAGCGATTCTCCCG T C AL604028.1,IPP Ensembl:ENSG00000230896,Ensembl:ENSG00000197429 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs566559813 Functional Loss SNV dbSNP153 33..33 33 - - - 42875 RMVar_ID_42875 Human_SNP_ID_11806902 A-to-I Human chr1 - 45697446 45697446 45697446 GGAGTTCAAGACCAGTCTTGCCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTGG GGAGTTCAAGACCAGTCTTGCCAACATGGTGAGACCCCGTCTCTACTAAAAATACAAAAAATTGG T C IPP Ensembl:ENSG00000197429 Protein coding intron GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs568585388 Functional Loss SNV dbSNP153 33..33 33 - - - 42876 RMVar_ID_42876 Human_SNP_ID_11806903 A-to-I Human chr1 - 45697446 45697446 45697446 GGAGTTCAAGACCAGTCTTGCCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTGG GGAGTTCAAGACCAGTCTTGCCAACATGGTGACACCCCGTCTCTACTAAAAATACAAAAAATTGG T G IPP Ensembl:ENSG00000197429 Protein coding intron GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs568585388 Functional Loss SNV dbSNP153 33..33 33 - - - 42877 RMVar_ID_42877 Human_SNP_ID_11806918 A-to-I Human chr1 - 45697494 45697494 45697494 TAATCCTAGCACTTTGGGAGACTGAGGTGGGCAGATCACTTGAGGTCAGGAGTTCAAGACCAGTC TAATCCTAGCACTTTGGGAGACTGAGGTGGGCTGATCACTTGAGGTCAGGAGTTCAAGACCAGTC T A IPP Ensembl:ENSG00000197429 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1362618817 Functional Loss SNV dbSNP153 33..33 33 - - - 42878 RMVar_ID_42878 Human_SNP_ID_11806986 A-to-I Human chr1 - 45697809 45697809 45697809 GGATTACAGACGTGAGCCACCATGCCTGGCTAATTTTTTGTATCTTTAGTAGAGACGGAGTTTCA GGATTACAGACGTGAGCCACCATGCCTGGCTAGTTTTTTGTATCTTTAGTAGAGACGGAGTTTCA T C IPP Ensembl:ENSG00000197429 Protein coding intron GSE38233;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,32596459 RNA-Seq:(High) rs1394162866 Functional Loss SNV dbSNP153 33..33 33 - - - 42879 RMVar_ID_42879 Human_SNP_ID_11807010 A-to-I Human chr1 - 45697874 45697874 45697874 AGCTCACTGCAACCTCTGCCTCCCTGGTTCAAACGATTCTCCCGCCTCAGCCTCCCGAGTAACTG AGCTCACTGCAACCTCTGCCTCCCTGGTTCAAGCGATTCTCCCGCCTCAGCCTCCCGAGTAACTG T C IPP Ensembl:ENSG00000197429 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1254647208 Functional Loss SNV dbSNP153 33..33 33 - - - 42880 RMVar_ID_42880 Human_SNP_ID_11807016 A-to-I Human chr1 - 45697906 45697906 45697906 TCACTCAGGCTGGAGTGCAATGGTGTGATCTCAGCTCACTGCAACCTCTGCCTCCCTGGTTCAAA TCACTCAGGCTGGAGTGCAATGGTGTGATCTCGGCTCACTGCAACCTCTGCCTCCCTGGTTCAAA T C IPP Ensembl:ENSG00000197429 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1428111571 Functional Loss SNV dbSNP153 33..33 33 - - - 42881 RMVar_ID_42881 Human_SNP_ID_11807061 A-to-I Human chr1 - 45698046 45698046 45698046 CACCTGCCTTGGCCTCCTGAAGTGCTGGGATTACAGGCATGGGCCAGCGTGCCCGGCTGCATACA CACCTGCCTTGGCCTCCTGAAGTGCTGGGATTGCAGGCATGGGCCAGCGTGCCCGGCTGCATACA T C IPP Ensembl:ENSG00000197429 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1390640019 Functional Loss SNV dbSNP153 33..33 33 - - - 42882 RMVar_ID_42882 Human_SNP_ID_11807079 A-to-I Human chr1 - 45698120 45698120 45698120 GCCTAGCTAATTTTTCTGTATGGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCT GCCTAGCTAATTTTTCTGTATGGGGTTTCACCTTGTTGGCCAGGCTGGTCTCGAACTCCTGACCT T A IPP Ensembl:ENSG00000197429 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1434748102 Functional Loss SNV dbSNP153 33..33 33 - - - 42883 RMVar_ID_42883 Human_SNP_ID_11807133 A-to-I Human chr1 - 45698291 45698290 45698291 GTCTTGCATACAGTAAAAAAAATTTTTTTTTGAGATGGAATTTTGCTCTTGTTGCCCAGGCTGGA GTCTTGCATACAGTAAAAAAAATTTTTTTTTG_GATGGAATTTTGCTCTTGTTGCCCAGGCTGGA CT C IPP Ensembl:ENSG00000197429 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1352428399 Functional Loss DEL dbSNP153 33..33 33 - - - 42884 RMVar_ID_42884 Human_SNP_ID_11807300 A-to-I Human chr1 - 45698883 45698883 45698883 ACTCCGTCTCTACCAAAAAATATATAAAAATTAGCCGGGCGTTGTGGCTTGTACCTGTGGTCCCA ACTCCGTCTCTACCAAAAAATATATAAAAATTGGCCGGGCGTTGTGGCTTGTACCTGTGGTCCCA T C IPP Ensembl:ENSG00000197429 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1263722305 Functional Loss SNV dbSNP153 33..33 33 - - - 42885 RMVar_ID_42885 Human_SNP_ID_11807301 A-to-I Human chr1 - 45698886 45698886 45698886 GAGACTCCGTCTCTACCAAAAAATATATAAAAATTAGCCGGGCGTTGTGGCTTGTACCTGTGGTC GAGACTCCGTCTCTACCAAAAAATATATAAAAGTTAGCCGGGCGTTGTGGCTTGTACCTGTGGTC T C IPP Ensembl:ENSG00000197429 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984891792 Functional Loss SNV dbSNP153 33..33 33 - - - 42886 RMVar_ID_42886 Human_SNP_ID_11807313 A-to-I Human chr1 - 45698925 45698925 45698925 TTGAACTCAGGAGTTCGAGACTAGCCTGGGCAACGTGATGAGACTCCGTCTCTACCAAAAAATAT TTGAACTCAGGAGTTCGAGACTAGCCTGGGCACCGTGATGAGACTCCGTCTCTACCAAAAAATAT T G IPP Ensembl:ENSG00000197429 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985820485 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26380872 42887 RMVar_ID_42887 Human_SNP_ID_11807334 A-to-I Human chr1 - 45698999 45698999 45698999 TTTTAGGCTGGGCATGGTGGCTCACACCTGTAATCCCAGCACTTTGAGAGGCCGAGGTGAGACGG TTTTAGGCTGGGCATGGTGGCTCACACCTGTAGTCCCAGCACTTTGAGAGGCCGAGGTGAGACGG T C IPP Ensembl:ENSG00000197429 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1135262 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8168013 42888 RMVar_ID_42888 Human_SNP_ID_11807335 A-to-I Human chr1 - 45699000 45699000 45699000 TTTTTAGGCTGGGCATGGTGGCTCACACCTGTAATCCCAGCACTTTGAGAGGCCGAGGTGAGACG TTTTTAGGCTGGGCATGGTGGCTCACACCTGTGATCCCAGCACTTTGAGAGGCCGAGGTGAGACG T C IPP Ensembl:ENSG00000197429 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1135261 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8168013 42889 RMVar_ID_42889 Human_SNP_ID_11809536 A-to-I Human chr1 - 45708567 45708567 45708567 TCAAGTGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGTATTACAGGTGTGTACCACCACACTTG TCAAGTGATTCTCCTGCCTCAGCCTCCTGAGTGGCTGGTATTACAGGTGTGTACCACCACACTTG T C IPP Ensembl:ENSG00000197429 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1222628373 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47978,RMVar_hsa_circ_17135,RMVar_hsa_circ_36348 42890 RMVar_ID_42890 Human_SNP_ID_11809863 A-to-I Human chr1 - 45709588 45709588 45709588 TGCCCTCCTCAGCCTCCCAAAGTGTTGGGATTACAGGCGTGAACCACCGTGCCCAGTTGAGAATG TGCCCTCCTCAGCCTCCCAAAGTGTTGGGATTGCAGGCGTGAACCACCGTGCCCAGTTGAGAATG T C IPP Ensembl:ENSG00000197429 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs979498212 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47978,RMVar_hsa_circ_17135,RMVar_hsa_circ_36348 42891 RMVar_ID_42891 Human_SNP_ID_11810532 A-to-I Human chr1 - 45712095 45712095 45712095 GCCAGACTGGTCTCGAACTCATGACCTCAAGCAATCCACCCGACTCGGCCTTCCAAAGTGCTGGA GCCAGACTGGTCTCGAACTCATGACCTCAAGCTATCCACCCGACTCGGCCTTCCAAAGTGCTGGA T A IPP Ensembl:ENSG00000197429 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1327184898 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47978,RMVar_hsa_circ_17135,RMVar_hsa_circ_36348 42892 RMVar_ID_42892 Human_SNP_ID_11810576 A-to-I Human chr1 - 45712298 45712298 45712298 AAGTCAAGTTGGTTGCTTTTTTTTTTTTTTTTAGACGTCGTCTTGCTCAGTCACCAGGCTGCTCA AAGTCAAGTTGGTTGCTTTTTTTTTTTTTTTTTGACGTCGTCTTGCTCAGTCACCAGGCTGCTCA T A IPP Ensembl:ENSG00000197429 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1187981159 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47978,RMVar_hsa_circ_17135,RMVar_hsa_circ_36348 42893 RMVar_ID_42893 Human_SNP_ID_11811003 A-to-I Human chr1 - 45713854 45713854 45713854 TTAATTAAAAAAAAAACTTTTTTTGTACTGCTAGGCGTGGTGGCCCACGCCTGTAATCCCAGCAC TTAATTAAAAAAAAAACTTTTTTTGTACTGCTGGGCGTGGTGGCCCACGCCTGTAATCCCAGCAC T C IPP Ensembl:ENSG00000197429 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1395639543 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47978,RMVar_hsa_circ_17135,RMVar_hsa_circ_36348 42894 RMVar_ID_42894 Human_SNP_ID_11811635 A-to-I Human chr1 - 45716448 45716448 45716448 CTGAGGTTAGGAGTTCGAGACCATCCTGGCCAACGTGGTGAAACCTCATTTCTACTAAAAATACA CTGAGGTTAGGAGTTCGAGACCATCCTGGCCAGCGTGGTGAAACCTCATTTCTACTAAAAATACA T C IPP Ensembl:ENSG00000197429 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1221733162 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47978,RMVar_hsa_circ_132568,RMVar_hsa_circ_17135,RMVar_hsa_circ_36348,RMVar_hsa_circ_323166,RMVar_hsa_circ_344159,RMVar_hsa_circ_291579,RMVar_hsa_circ_132566,RMVar_hsa_circ_132567 42895 RMVar_ID_42895 Human_SNP_ID_11815078 A-to-I Human chr1 - 45728714 45728714 45728714 AGGTGGGAGGATGGTGTGAGCCCAGAAGTTCAAGACCAGTCTAGGCAACATGATGAAACCTTGTC AGGTGGGAGGATGGTGTGAGCCCAGAAGTTCAGGACCAGTCTAGGCAACATGATGAAACCTTGTC T C IPP Ensembl:ENSG00000197429 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1250132596 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17135,RMVar_hsa_circ_344159,RMVar_hsa_circ_132566,RMVar_hsa_circ_341206,RMVar_hsa_circ_12034,RMVar_hsa_circ_132570,RMVar_hsa_circ_132571,RMVar_hsa_circ_294654 42896 RMVar_ID_42896 Human_SNP_ID_11845865 A-to-I Human chr1 + 45847463 45847463 45847463 TTTTGAAACCATTGCAGTTTTTCACCAATAAGATTGAAACACAAGGCCTTTTCATTCTTCAATTT TTTTGAAACCATTGCAGTTTTTCACCAATAAGGTTGAAACACAAGGCCTTTTCATTCTTCAATTT A G MAST2 Ensembl:ENSG00000086015 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017798736 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84369,RMVar_hsa_circ_329622,RMVar_hsa_circ_132575,RMVar_hsa_circ_132576,RMVar_hsa_circ_370985 42897 RMVar_ID_42897 Human_SNP_ID_11845866 A-to-I Human chr1 + 45847463 45847463 45847463 TTTTGAAACCATTGCAGTTTTTCACCAATAAGATTGAAACACAAGGCCTTTTCATTCTTCAATTT TTTTGAAACCATTGCAGTTTTTCACCAATAAGTTTGAAACACAAGGCCTTTTCATTCTTCAATTT A T MAST2 Ensembl:ENSG00000086015 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017798736 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84369,RMVar_hsa_circ_329622,RMVar_hsa_circ_132575,RMVar_hsa_circ_132576,RMVar_hsa_circ_370985 42898 RMVar_ID_42898 Human_SNP_ID_11845868 A-to-I Human chr1 + 45847471 45847471 45847471 CCATTGCAGTTTTTCACCAATAAGATTGAAACACAAGGCCTTTTCATTCTTCAATTTTTCCTTTT CCATTGCAGTTTTTCACCAATAAGATTGAAACGCAAGGCCTTTTCATTCTTCAATTTTTCCTTTT A G MAST2 Ensembl:ENSG00000086015 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs989218838 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84369,RMVar_hsa_circ_329622,RMVar_hsa_circ_132575,RMVar_hsa_circ_132576,RMVar_hsa_circ_370985 42899 RMVar_ID_42899 Human_SNP_ID_11845875 A-to-I Human chr1 + 45847510 45847510 45847510 CTTTTCATTCTTCAATTTTTCCTTTTTTTCTTATTTGTGGGCCTCTCTCATAATTTGAGCTGCTT CTTTTCATTCTTCAATTTTTCCTTTTTTTCTTGTTTGTGGGCCTCTCTCATAATTTGAGCTGCTT A G MAST2 Ensembl:ENSG00000086015 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs927878320 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5831588 RMVar_hsa_circ_84369,RMVar_hsa_circ_329622,RMVar_hsa_circ_132575,RMVar_hsa_circ_132576,RMVar_hsa_circ_370985 42900 RMVar_ID_42900 Human_SNP_ID_11845884 A-to-I Human chr1 + 45847527 45847527 45847527 TTTCCTTTTTTTCTTATTTGTGGGCCTCTCTCATAATTTGAGCTGCTTTTCTACTATATGGATGA TTTCCTTTTTTTCTTATTTGTGGGCCTCTCTCGTAATTTGAGCTGCTTTTCTACTATATGGATGA A G MAST2 Ensembl:ENSG00000086015 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1214302941 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84369,RMVar_hsa_circ_329622,RMVar_hsa_circ_132575,RMVar_hsa_circ_132576,RMVar_hsa_circ_370985 42901 RMVar_ID_42901 Human_SNP_ID_11855621 A-to-I Human chr1 + 45887075 45887075 45887075 GTCTGGAACTCCTGAGCTCAAGCTATCTGCCTACCTTGGCTTCCCAAAGTGCTTAGATTACAGGC GTCTGGAACTCCTGAGCTCAAGCTATCTGCCTGCCTTGGCTTCCCAAAGTGCTTAGATTACAGGC A G MAST2 Ensembl:ENSG00000086015 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404904044 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_329622,RMVar_hsa_circ_104755,RMVar_hsa_circ_318686,RMVar_hsa_circ_132577,RMVar_hsa_circ_132578 42902 RMVar_ID_42902 Human_SNP_ID_11871355 A-to-I Human chr1 + 45948613 45948613 45948613 TCTGTAGTCTCAGCTACCTGGGAGGCTGAGGCAGGAGAATTGCTTGAACCTGGGAGGTGAAGATT TCTGTAGTCTCAGCTACCTGGGAGGCTGAGGCGGGAGAATTGCTTGAACCTGGGAGGTGAAGATT A G MAST2 Ensembl:ENSG00000086015 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs994523277 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_329622,RMVar_hsa_circ_41672,RMVar_hsa_circ_86756,RMVar_hsa_circ_104755,RMVar_hsa_circ_318686,RMVar_hsa_circ_132577,RMVar_hsa_circ_132578,RMVar_hsa_circ_132579,RMVar_hsa_circ_103987,RMVar_hsa_circ_132580,RMVar_hsa_circ_370914,RMVar_hsa_circ_277225,RMVar_hsa_circ_132583,RMVar_hsa_circ_132585,RMVar_hsa_circ_57922,RMVar_hsa_circ_132584 42903 RMVar_ID_42903 Human_SNP_ID_11884002 A-to-I Human chr1 + 46000193 46000187 46000194 AAAATTAGCCGGGCATGGTGGTGCAGGTCTGTAATCCTAGCTGCTCGGGAGGCTGAGGCAGGAGA AAAATTAGCCGGGCATGGTGGTGCAGG_______TCCTAGCTGCTCGGGAGGCTGAGGCAGGAGA GTCTGTAA G MAST2 Ensembl:ENSG00000086015 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1313809199 Functional Loss DEL dbSNP153 28..34 33 - - - RMVar_hsa_circ_104755,RMVar_hsa_circ_132578,RMVar_hsa_circ_103987,RMVar_hsa_circ_132585,RMVar_hsa_circ_57922,RMVar_hsa_circ_14560,RMVar_hsa_circ_97894,RMVar_hsa_circ_10047,RMVar_hsa_circ_297884,RMVar_hsa_circ_314321,RMVar_hsa_circ_112346,RMVar_hsa_circ_52601,RMVar_hsa_circ_132588,RMVar_hsa_circ_132589,RMVar_hsa_circ_132590,RMVar_hsa_circ_132587 42904 RMVar_ID_42904 Human_SNP_ID_11894567 A-to-I Human chr1 - 46040330 46040327 46040330 TGTATGTCTTGTGATGGGACAGTTCATAATGTAGTTGCTAGACCACTTTACAAATTGTTCTTGTC TGTATGTCTTGTGATGGGACAGTTCATAATGT___TGCTAGACCACTTTACAAATTGTTCTTGTC AACT A PIK3R3 Ensembl:ENSG00000117461 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1167288624 Functional Loss DEL dbSNP153 33..35 33 - - - 42905 RMVar_ID_42905 Human_SNP_ID_11896681 A-to-I Human chr1 - 46049098 46049098 46049098 CAAGACCATGCCAAAAAATATGTATATATAGTATCTTTTCTAAAAATCTAATTGGTTTTACAACC CAAGACCATGCCAAAAAATATGTATATATAGTGTCTTTTCTAAAAATCTAATTGGTTTTACAACC T C PIK3R3,P3R3URF-PIK3R3 Ensembl:ENSG00000117461,Ensembl:ENSG00000278139 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1239199407 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_132601,RMVar_hsa_circ_315669,RMVar_hsa_circ_329213,RMVar_hsa_circ_334230,RMVar_hsa_circ_60573,RMVar_hsa_circ_132602,RMVar_hsa_circ_40147,RMVar_hsa_circ_132603 42906 RMVar_ID_42906 Human_SNP_ID_11897846 A-to-I Human chr1 - 46054131 46054125 46054131 CCTTGGCCTCCTAAAGTACTGGGATTATAGGCATGAGCTACTGTACCCAGCCTAAGGTGATATTT CCTTGGCCTCCTAAAGTACTGGGATTATAGGC______TACTGTACCCAGCCTAAGGTGATATTT AGCTCAT A PIK3R3,P3R3URF-PIK3R3 Ensembl:ENSG00000117461,Ensembl:ENSG00000278139 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1165108842 Functional Loss DEL dbSNP153 33..38 33 - - - RMVar_hsa_circ_132601,RMVar_hsa_circ_315669,RMVar_hsa_circ_329213,RMVar_hsa_circ_334230,RMVar_hsa_circ_60573,RMVar_hsa_circ_132602,RMVar_hsa_circ_40147,RMVar_hsa_circ_132603 42907 RMVar_ID_42907 Human_SNP_ID_11897847 A-to-I Human chr1 - 46054131 46054131 46054131 CCTTGGCCTCCTAAAGTACTGGGATTATAGGCATGAGCTACTGTACCCAGCCTAAGGTGATATTT CCTTGGCCTCCTAAAGTACTGGGATTATAGGCGTGAGCTACTGTACCCAGCCTAAGGTGATATTT T C PIK3R3,P3R3URF-PIK3R3 Ensembl:ENSG00000117461,Ensembl:ENSG00000278139 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1422851753 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_132601,RMVar_hsa_circ_315669,RMVar_hsa_circ_329213,RMVar_hsa_circ_334230,RMVar_hsa_circ_60573,RMVar_hsa_circ_132602,RMVar_hsa_circ_40147,RMVar_hsa_circ_132603 42908 RMVar_ID_42908 Human_SNP_ID_11898118 A-to-I Human chr1 - 46055273 46055273 46055273 TGAAACTCCGTTTCTACTAAAAATACAAAATTAGCTGGGCGTGGTGGCACATTCTTGTAATCCCA TGAAACTCCGTTTCTACTAAAAATACAAAATTGGCTGGGCGTGGTGGCACATTCTTGTAATCCCA T C PIK3R3,P3R3URF-PIK3R3 Ensembl:ENSG00000117461,Ensembl:ENSG00000278139 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs577465075 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_132601,RMVar_hsa_circ_315669,RMVar_hsa_circ_329213,RMVar_hsa_circ_334230,RMVar_hsa_circ_60573,RMVar_hsa_circ_132602,RMVar_hsa_circ_40147,RMVar_hsa_circ_132603 42909 RMVar_ID_42909 Human_SNP_ID_11898398 A-to-I Human chr1 - 46056339 46056339 46056339 ACGCTTAAGATATTAGGACCTCACTGGGTGCAATGGCTCACGCCTGTAATCCCAGTACTTTGGGA ACGCTTAAGATATTAGGACCTCACTGGGTGCAGTGGCTCACGCCTGTAATCCCAGTACTTTGGGA T C PIK3R3,P3R3URF-PIK3R3 Ensembl:ENSG00000117461,Ensembl:ENSG00000278139 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs373747837 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_132601,RMVar_hsa_circ_315669,RMVar_hsa_circ_329213,RMVar_hsa_circ_334230,RMVar_hsa_circ_60573,RMVar_hsa_circ_313587,RMVar_hsa_circ_132602,RMVar_hsa_circ_40147,RMVar_hsa_circ_132603,RMVar_hsa_circ_355083,RMVar_hsa_circ_322801,RMVar_hsa_circ_270585,RMVar_hsa_circ_275672,RMVar_hsa_circ_49355,RMVar_hsa_circ_132605,RMVar_hsa_circ_132607,RMVar_hsa_circ_132608,RMVar_hsa_circ_132606 42910 RMVar_ID_42910 Human_SNP_ID_11903857 A-to-I Human chr1 - 46079697 46079697 46079697 CACCTACCTTGGCCTCCCAAAGTGCTGGGATTACAGGTGTAAGCCACTGCACCTGGCTGAAAATC CACCTACCTTGGCCTCCCAAAGTGCTGGGATTGCAGGTGTAAGCCACTGCACCTGGCTGAAAATC T C PIK3R3,P3R3URF-PIK3R3 Ensembl:ENSG00000117461,Ensembl:ENSG00000278139 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1309681688 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24703197 RMVar_hsa_circ_132601,RMVar_hsa_circ_315669,RMVar_hsa_circ_40147,RMVar_hsa_circ_132603,RMVar_hsa_circ_270585,RMVar_hsa_circ_49355,RMVar_hsa_circ_132605,RMVar_hsa_circ_349567,RMVar_hsa_circ_285279,RMVar_hsa_circ_132610,RMVar_hsa_circ_132611,RMVar_hsa_circ_318105,RMVar_hsa_circ_282439,RMVar_hsa_circ_132612,RMVar_hsa_circ_292068,RMVar_hsa_circ_132613 42911 RMVar_ID_42911 Human_SNP_ID_11906441 A-to-I Human chr1 - 46091281 46091281 46091281 CAAAAATTAGCTGGGCGTGATAGCACGTGCCTATAGTCCCAGCTCCTTGGGAGGCTGAGACAGGA CAAAAATTAGCTGGGCGTGATAGCACGTGCCTGTAGTCCCAGCTCCTTGGGAGGCTGAGACAGGA T C PIK3R3,P3R3URF-PIK3R3 Ensembl:ENSG00000117461,Ensembl:ENSG00000278139 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs533084336 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_315669,RMVar_hsa_circ_49355,RMVar_hsa_circ_349567,RMVar_hsa_circ_132611,RMVar_hsa_circ_292068 42912 RMVar_ID_42912 Human_SNP_ID_11910702 A-to-I Human chr1 - 46108970 46108970 46108970 TATTTTTAGTAGAGACACGGTTTCACCGTGTTAGCCAGGATAGTCTCGATCTCCTGACCTCGTGA TATTTTTAGTAGAGACACGGTTTCACCGTGTTGGCCAGGATAGTCTCGATCTCCTGACCTCGTGA T C PIK3R3,P3R3URF-PIK3R3 Ensembl:ENSG00000117461,Ensembl:ENSG00000278139 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946674925 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_315669,RMVar_hsa_circ_49355,RMVar_hsa_circ_349567,RMVar_hsa_circ_132611,RMVar_hsa_circ_292068 42913 RMVar_ID_42913 Human_SNP_ID_11910865 A-to-I Human chr1 - 46109522 46109522 46109522 CTGAGATTGCGTCACTGTACTTCAGCCTGGGCAACAGGCGGAGACTCCATCTCAAAAAAAAACAA CTGAGATTGCGTCACTGTACTTCAGCCTGGGCTACAGGCGGAGACTCCATCTCAAAAAAAAACAA T A PIK3R3,P3R3URF-PIK3R3 Ensembl:ENSG00000117461,Ensembl:ENSG00000278139 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs758088006 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_315669,RMVar_hsa_circ_49355,RMVar_hsa_circ_349567,RMVar_hsa_circ_132611,RMVar_hsa_circ_292068 42914 RMVar_ID_42914 Human_SNP_ID_11912811 A-to-I Human chr1 - 46117995 46117995 46117995 CAGCTCACTGTAGCCTTGACCTCCTGGGCTCAAGTGGTCCTCCCACCTTAGCCTTCTGAGTAGCT CAGCTCACTGTAGCCTTGACCTCCTGGGCTCAGGTGGTCCTCCCACCTTAGCCTTCTGAGTAGCT T C PIK3R3,P3R3URF-PIK3R3 Ensembl:ENSG00000117461,Ensembl:ENSG00000278139 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1173566462 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_315669,RMVar_hsa_circ_49355,RMVar_hsa_circ_349567,RMVar_hsa_circ_132611,RMVar_hsa_circ_292068 42915 RMVar_ID_42915 Human_SNP_ID_11914798 A-to-I Human chr1 - 46126426 46126426 46126426 TCATGCAATTCTCCTGCCTCAGCCACCTGAGTAGCTGGGGTTACAGGTGCCTACCACCATGCCTG TCATGCAATTCTCCTGCCTCAGCCACCTGAGTTGCTGGGGTTACAGGTGCCTACCACCATGCCTG T A PIK3R3,P3R3URF-PIK3R3 Ensembl:ENSG00000117461,Ensembl:ENSG00000278139 Protein coding,Protein coding intron,intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1557637050 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_315669,RMVar_hsa_circ_49355,RMVar_hsa_circ_349567,RMVar_hsa_circ_132611,RMVar_hsa_circ_292068 42916 RMVar_ID_42916 Human_SNP_ID_11915323 A-to-I Human chr1 - 46128374 46128374 46128374 GGAGTGCAGTGGCTCTATCTCGGCTCACTGCAACCTCCACATCCTGGGTTCAAAGGATTCTTGTC GGAGTGCAGTGGCTCTATCTCGGCTCACTGCAGCCTCCACATCCTGGGTTCAAAGGATTCTTGTC T C PIK3R3,P3R3URF-PIK3R3 Ensembl:ENSG00000117461,Ensembl:ENSG00000278139 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1352138529 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_315669,RMVar_hsa_circ_49355,RMVar_hsa_circ_349567,RMVar_hsa_circ_132611,RMVar_hsa_circ_292068 42917 RMVar_ID_42917 Human_SNP_ID_11950034 A-to-I Human chr1 + 46268795 46268795 46268795 TTCTACTGGTTTGGTTTTGTTTGTTGAGACAGAGTCTCTGTTGCCCAGGCTGGAGTACAGCGTTG TTCTACTGGTTTGGTTTTGTTTGTTGAGACAGGGTCTCTGTTGCCCAGGCTGGAGTACAGCGTTG A G RAD54L Ensembl:ENSG00000085999 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs896009135 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1749196,Human_RBP_ID_11010921 RMVar_hsa_circ_50139,RMVar_hsa_circ_82919,RMVar_hsa_circ_113076,RMVar_hsa_circ_132634,RMVar_hsa_circ_132633,RMVar_hsa_circ_325696 42918 RMVar_ID_42918 Human_SNP_ID_11950059 A-to-I Human chr1 + 46268931 46268928 46268932 GGGACTACAGGCATATGCCACCACTATTGGCTAACTTTTAAATTTTTTATAGAGATGGGGTCTCA GGGACTACAGGCATATGCCACCACTATTGG____CTTTTAAATTTTTTATAGAGATGGGGTCTCA GCTAA G RAD54L Ensembl:ENSG00000085999 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1480920478 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_11010923 RMVar_hsa_circ_50139,RMVar_hsa_circ_82919,RMVar_hsa_circ_113076,RMVar_hsa_circ_132634,RMVar_hsa_circ_132633,RMVar_hsa_circ_325696 42919 RMVar_ID_42919 Human_SNP_ID_11953924 A-to-I Human chr1 - 46283464 46283464 46283464 CAACTCATTACATCCAACTTGAATGCATTTTTATATTTTTAGTAAGGACAGGGTTTCCCCATATA CAACTCATTACATCCAACTTGAATGCATTTTTGTATTTTTAGTAAGGACAGGGTTTCCCCATATA T C LRRC41 Ensembl:ENSG00000132128 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1405493682 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50692,RMVar_hsa_circ_311835,RMVar_hsa_circ_368668,RMVar_hsa_circ_132639,RMVar_hsa_circ_87705,RMVar_hsa_circ_132640 42920 RMVar_ID_42920 Human_SNP_ID_11955684 A-to-I Human chr1 - 46290186 46290186 46290186 CCAGGCTGATCACAAACTCATGGACTCAAGCAATCTGCCCACCTTGGCATCCCCAAGTACTGCGA CCAGGCTGATCACAAACTCATGGACTCAAGCAGTCTGCCCACCTTGGCATCCCCAAGTACTGCGA T C LRRC41 Ensembl:ENSG00000132128 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1169572088 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50692,RMVar_hsa_circ_311835,RMVar_hsa_circ_368668,RMVar_hsa_circ_132639,RMVar_hsa_circ_26204 42921 RMVar_ID_42921 Human_SNP_ID_11955685 A-to-I Human chr1 - 46290187 46290187 46290187 CCCAGGCTGATCACAAACTCATGGACTCAAGCAATCTGCCCACCTTGGCATCCCCAAGTACTGCG CCCAGGCTGATCACAAACTCATGGACTCAAGCCATCTGCCCACCTTGGCATCCCCAAGTACTGCG T G LRRC41 Ensembl:ENSG00000132128 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1046668611 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50692,RMVar_hsa_circ_311835,RMVar_hsa_circ_368668,RMVar_hsa_circ_132639,RMVar_hsa_circ_26204 42922 RMVar_ID_42922 Human_SNP_ID_11955696 A-to-I Human chr1 - 46290245 46290245 46290245 CCACTATGCCCAGCTACATTTTTTCTATTTTTAGTAGAGATAGGGTTTTGTCACATTGCCCAGGC CCACTATGCCCAGCTACATTTTTTCTATTTTTGGTAGAGATAGGGTTTTGTCACATTGCCCAGGC T C LRRC41 Ensembl:ENSG00000132128 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1334113440 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50692,RMVar_hsa_circ_311835,RMVar_hsa_circ_368668,RMVar_hsa_circ_132639,RMVar_hsa_circ_26204 42923 RMVar_ID_42923 Human_SNP_ID_11955970 A-to-I Human chr1 + 46291004 46291004 46291004 TGGAGTACAGTGGCACGATCTCGGCTCACTGCAACCTCCATCTCCCAGGTTCAAGCTATTCTCCT TGGAGTACAGTGGCACGATCTCGGCTCACTGCGACCTCCATCTCCCAGGTTCAAGCTATTCTCCT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984032273 Functional Loss SNV dbSNP153 33..33 33 - - - 42924 RMVar_ID_42924 Human_SNP_ID_11956675 A-to-I Human chr1 - 46293926 46293926 46293926 AAACCCTGTCTCTACTGAAAATCAGGCATGGTAGTGCATGCCTGTAATCCCAGCTACTCTGGGAT AAACCCTGTCTCTACTGAAAATCAGGCATGGTGGTGCATGCCTGTAATCCCAGCTACTCTGGGAT T C LRRC41 Ensembl:ENSG00000132128 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs998887268 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50692,RMVar_hsa_circ_311835,RMVar_hsa_circ_368668,RMVar_hsa_circ_132639,RMVar_hsa_circ_26204 42925 RMVar_ID_42925 Human_SNP_ID_11956749 A-to-I Human chr1 - 46294246 46294246 46294246 AAAATTATCCTGTTGTGGTGTTGTGCACCTGTAGTCCCAGCTACTCAGGAGGCTGAGGTGGGAGG AAAATTATCCTGTTGTGGTGTTGTGCACCTGTGGTCCCAGCTACTCAGGAGGCTGAGGTGGGAGG T C LRRC41 Ensembl:ENSG00000132128 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs760761868 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50692,RMVar_hsa_circ_311835,RMVar_hsa_circ_368668,RMVar_hsa_circ_132639,RMVar_hsa_circ_26204 42926 RMVar_ID_42926 Human_SNP_ID_11959460 A-to-I Human chr1 + 46305042 46305042 46305042 TCTAAAAAGAAATAGAACCTGAGGCCGGGCGCAGTGGCTCACGCCTGTAATCCCAACACTTTAGG TCTAAAAAGAAATAGAACCTGAGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAACACTTTAGG A G UQCRH Ensembl:ENSG00000173660 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1039885607 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11011992,Human_RBP_ID_17557858 RMVar_hsa_circ_75543,RMVar_hsa_circ_132645 42927 RMVar_ID_42927 Human_SNP_ID_11959731 A-to-I Human chr1 + 46305935 46305935 46305935 AAGCGATTCTCTTTTGCCTCAGCCTCCTGAGTAGCTGAAATTACAGGCGCACGCCACCTAATTTT AAGCGATTCTCTTTTGCCTCAGCCTCCTGAGTGGCTGAAATTACAGGCGCACGCCACCTAATTTT A G UQCRH Ensembl:ENSG00000173660 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1484492653 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75543,RMVar_hsa_circ_132645 42928 RMVar_ID_42928 Human_SNP_ID_11959874 A-to-I Human chr1 + 46306432 46306432 46306432 GTGACGGAGTCTCGCTCTTGCCTGGCTGGAGTACAGTGGCGCGATCTCACTGCAACCTCTGCCTC GTGACGGAGTCTCGCTCTTGCCTGGCTGGAGTGCAGTGGCGCGATCTCACTGCAACCTCTGCCTC A G UQCRH Ensembl:ENSG00000173660 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1019889287 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17558387 RMVar_hsa_circ_75543,RMVar_hsa_circ_132645 42929 RMVar_ID_42929 Human_SNP_ID_11959929 A-to-I Human chr1 + 46306632 46306632 46306632 TTGACCTCGTGATCCTCCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGACATGAGCCACTGCA TTGACCTCGTGATCCTCCTGCCTTGGCCTCCCGAAGTGCTGGGATTACAGACATGAGCCACTGCA A G UQCRH Ensembl:ENSG00000173660 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1047197041 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24703976 RMVar_hsa_circ_75543,RMVar_hsa_circ_132645 42930 RMVar_ID_42930 Human_SNP_ID_11959932 A-to-I Human chr1 + 46306646 46306645 46306647 CTCCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGACATGAGCCACTGCACCCGGCTTTCAGTA CTCCTGCCTTGGCCTCCCAAAGTGCTGGGATT__AGACATGAGCCACTGCACCCGGCTTTCAGTA TAC T UQCRH Ensembl:ENSG00000173660 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1345568902 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_75543,RMVar_hsa_circ_132645 42931 RMVar_ID_42931 Human_SNP_ID_11961327 A-to-I Human chr1 + 46311850 46311850 46311850 CGGGGTTTCACTGTGTTAGCCAAGATGGTCTCAGTCTCCTGACCCCTGTGATCCACCTGCCTCAG CGGGGTTTCACTGTGTTAGCCAAGATGGTCTCTGTCTCCTGACCCCTGTGATCCACCTGCCTCAG A T UQCRH Ensembl:ENSG00000173660 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1402532568 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127847,RMVar_hsa_circ_132647 42932 RMVar_ID_42932 Human_SNP_ID_11961369 A-to-I Human chr1 + 46311949 46311949 46311949 CTGCACCCAGCCTTTTTTTTTTTTTTTGAGATAAGGTCTTGCTTGCTCTGTCACCCAGGCTGGAG CTGCACCCAGCCTTTTTTTTTTTTTTTGAGATGAGGTCTTGCTTGCTCTGTCACCCAGGCTGGAG A G UQCRH Ensembl:ENSG00000173660 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1356712897 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11012144,Human_RBP_ID_17557863 RMVar_hsa_circ_127847,RMVar_hsa_circ_132647 42933 RMVar_ID_42933 Human_SNP_ID_11961388 A-to-I Human chr1 + 46312061 46312061 46312061 AACAATCCTTCTGCCTTAGCCTCTGAGTAGCCAGGACTATAGGCACATGCCACCATGCCTTGGTA AACAATCCTTCTGCCTTAGCCTCTGAGTAGCCGGGACTATAGGCACATGCCACCATGCCTTGGTA A G UQCRH Ensembl:ENSG00000173660 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973194629 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127847,RMVar_hsa_circ_132647 42934 RMVar_ID_42934 Human_SNP_ID_11961519 A-to-I Human chr1 + 46312605 46312605 46312605 TAAACTCAGGCAGGGCATAGTGGCTGACGCTTATGATCCTAGCACTTTTGGAAGACCAAGGCAGG TAAACTCAGGCAGGGCATAGTGGCTGACGCTTGTGATCCTAGCACTTTTGGAAGACCAAGGCAGG A G UQCRH Ensembl:ENSG00000173660 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350185324 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11012153 RMVar_hsa_circ_127847,RMVar_hsa_circ_132647 42935 RMVar_ID_42935 Human_SNP_ID_11961975 A-to-I Human chr1 + 46314255 46314255 46314255 GGGCATGGTGGCGGGTGCTTGTAGAACCAGCTACTTGGGAGGCTGAGGCAGGAGATTGGCATGAA GGGCATGGTGGCGGGTGCTTGTAGAACCAGCTCCTTGGGAGGCTGAGGCAGGAGATTGGCATGAA A C UQCRH Ensembl:ENSG00000173660 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs937958636 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127847,RMVar_hsa_circ_132647 42936 RMVar_ID_42936 Human_SNP_ID_11971148 A-to-I Human chr1 + 46347377 46347377 46347377 GGAGAATTGCTTGAACCCGGGAAGTGGAGGTTACAATGAGCTGAGATCCTGCCACTGCACTCCAG GGAGAATTGCTTGAACCCGGGAAGTGGAGGTTGCAATGAGCTGAGATCCTGCCACTGCACTCCAG A G NSUN4 Ensembl:ENSG00000117481 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs986124416 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94338,RMVar_hsa_circ_132649,RMVar_hsa_circ_305945 42937 RMVar_ID_42937 Human_SNP_ID_11971338 A-to-I Human chr1 + 46348071 46348071 46348071 AGCTAATTTGTTTTTGTACTTTTAGTAGAGACAGGGTTTCACCCTGTTAGCCAGGATGGTCTCAA AGCTAATTTGTTTTTGTACTTTTAGTAGAGACGGGGTTTCACCCTGTTAGCCAGGATGGTCTCAA A G NSUN4 Ensembl:ENSG00000117481 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs185635559 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94338,RMVar_hsa_circ_132649,RMVar_hsa_circ_305945 42938 RMVar_ID_42938 Human_SNP_ID_11971458 A-to-I Human chr1 + 46348455 46348455 46348455 TGGATTCTGGCCGGGCACGGTGGCTCACGCCTATAATTCCAGCACTTTGGAAGGCTGAGGCGGGT TGGATTCTGGCCGGGCACGGTGGCTCACGCCTGTAATTCCAGCACTTTGGAAGGCTGAGGCGGGT A G NSUN4 Ensembl:ENSG00000117481 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1240963141 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557865 RMVar_hsa_circ_94338,RMVar_hsa_circ_132649,RMVar_hsa_circ_305945 42939 RMVar_ID_42939 Human_SNP_ID_11971679 A-to-I Human chr1 + 46348918 46348918 46348918 CTCAATACAACCTTCGCCTTCTGGTTCCAAGCAATTCTCTTGCCTCAGCCTCCTGAGTAGCTGGG CTCAATACAACCTTCGCCTTCTGGTTCCAAGCGATTCTCTTGCCTCAGCCTCCTGAGTAGCTGGG A G NSUN4 Ensembl:ENSG00000117481 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs12562440 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_4971,GWAS_ID_4972,GWAS_ID_4973,GWAS_ID_4974,GWAS_ID_4975,GWAS_ID_4976,GWAS_ID_4977,GWAS_ID_4978,GWAS_ID_4979,GWAS_ID_4980,GWAS_ID_4981,GWAS_ID_4982 RMVar_hsa_circ_94338,RMVar_hsa_circ_132649,RMVar_hsa_circ_305945 42940 RMVar_ID_42940 Human_SNP_ID_11971681 A-to-I Human chr1 + 46348944 46348944 46348944 CCAAGCAATTCTCTTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCACCCACCACCACACCCG CCAAGCAATTCTCTTGCCTCAGCCTCCTGAGTGGCTGGGATTACAGGCACCCACCACCACACCCG A G NSUN4 Ensembl:ENSG00000117481 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1228889959 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94338,RMVar_hsa_circ_132649,RMVar_hsa_circ_305945 42941 RMVar_ID_42941 Human_SNP_ID_11972265 A-to-I Human chr1 + 46351303 46351303 46351303 GGAGAATCGCTTGAACCCGGGAGGCGGAGGTTATGGTAAGCCGAGATCGCGCCATTGCACTCTAG GGAGAATCGCTTGAACCCGGGAGGCGGAGGTTGTGGTAAGCCGAGATCGCGCCATTGCACTCTAG A G NSUN4 Ensembl:ENSG00000117481 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1442169331 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11012364 RMVar_hsa_circ_94338,RMVar_hsa_circ_132649,RMVar_hsa_circ_305945 42942 RMVar_ID_42942 Human_SNP_ID_11973522 A-to-I Human chr1 + 46356443 46356443 46356443 GGCTGGGCGCGGTGGCTCACGCCTGTATTCCCAGCACTTTGGGAGGCCAAGGCGGGCGGATCACG GGCTGGGCGCGGTGGCTCACGCCTGTATTCCCTGCACTTTGGGAGGCCAAGGCGGGCGGATCACG A T NSUN4 Ensembl:ENSG00000117481 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs983361717 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_96440 RMVar_hsa_circ_94338,RMVar_hsa_circ_132649,RMVar_hsa_circ_132651,RMVar_hsa_circ_53742 42943 RMVar_ID_42943 Human_SNP_ID_11973769 A-to-I Human chr1 + 46357357 46357357 46357357 ATGTGCCAGCATGTCCAGCTAATTTTTTTGGTATTTTTTGTGGAGACGGGGTTTTGTCATATTGC ATGTGCCAGCATGTCCAGCTAATTTTTTTGGTGTTTTTTGTGGAGACGGGGTTTTGTCATATTGC A G NSUN4 Ensembl:ENSG00000117481 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1045046812 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11012520 RMVar_hsa_circ_94338,RMVar_hsa_circ_132649,RMVar_hsa_circ_132651,RMVar_hsa_circ_53742 42944 RMVar_ID_42944 Human_SNP_ID_11975528 A-to-I Human chr1 + 46364021 46364021 46364021 TAGTCACCATCAAGATGTAGAAAATAGAAAATAGGCTAGGCACAGTGGCTCACGCCTGTAATCTC TAGTCACCATCAAGATGTAGAAAATAGAAAATGGGCTAGGCACAGTGGCTCACGCCTGTAATCTC A G NSUN4 Ensembl:ENSG00000117481 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs954118983 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_356790,Human_RBP_ID_11012679,Human_RBP_ID_23399170 RMVar_hsa_circ_94338,RMVar_hsa_circ_132649 42945 RMVar_ID_42945 Human_SNP_ID_11978012 A-to-I Human chr1 + 46374591 46374591 46374591 AGAGGGCGCCACTGCACTCCAGCCTGGACAACAGAGGGAGACTCTGTCTCAAAAAAAATTAAAAA AGAGGGCGCCACTGCACTCCAGCCTGGACAACGGAGGGAGACTCTGTCTCAAAAAAAATTAAAAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs530303377 Functional Loss SNV dbSNP153 33..33 33 - - - 42946 RMVar_ID_42946 Human_SNP_ID_12030789 A-to-I Human chr1 - 46586940 46586940 46586940 AGCCGGACATGGTGGCATGTGCCTGTAGTCCCAGCTACTCTGGAGGCTGAGGCAGGAGAATCGCT AGCCGGACATGGTGGCATGTGCCTGTAGTCCCGGCTACTCTGGAGGCTGAGGCAGGAGAATCGCT T C MKNK1 Ensembl:ENSG00000079277 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1400626149 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_95915 RMVar_hsa_circ_96009,RMVar_hsa_circ_111909,RMVar_hsa_circ_132657,RMVar_hsa_circ_132656,RMVar_hsa_circ_132663,RMVar_hsa_circ_78031,RMVar_hsa_circ_115021,RMVar_hsa_circ_132664,RMVar_hsa_circ_369331,RMVar_hsa_circ_132669,RMVar_hsa_circ_354932,RMVar_hsa_circ_281295 42947 RMVar_ID_42947 Human_SNP_ID_12030811 A-to-I Human chr1 - 46587011 46587011 46587011 GAGGTCAGGAGTTTGAGACCAGCCTGGCCAACATGGCGAAACCCCGTCTCTACTAAAAAGTACAA GAGGTCAGGAGTTTGAGACCAGCCTGGCCAACGTGGCGAAACCCCGTCTCTACTAAAAAGTACAA T C MKNK1 Ensembl:ENSG00000079277 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs972128262 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_95915 RMVar_hsa_circ_96009,RMVar_hsa_circ_111909,RMVar_hsa_circ_132657,RMVar_hsa_circ_132656,RMVar_hsa_circ_132663,RMVar_hsa_circ_78031,RMVar_hsa_circ_115021,RMVar_hsa_circ_132664,RMVar_hsa_circ_369331,RMVar_hsa_circ_132669,RMVar_hsa_circ_354932,RMVar_hsa_circ_281295 42948 RMVar_ID_42948 Human_SNP_ID_12031570 A-to-I Human chr1 - 46590320 46590320 46590320 GTCATGTGGACTCTAATACTGCTCCGGCTACTACTTCAAAGATGTAAATGTTCTGGGGTCAGTCT GTCATGTGGACTCTAATACTGCTCCGGCTACTGCTTCAAAGATGTAAATGTTCTGGGGTCAGTCT T C MKNK1 Ensembl:ENSG00000079277 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs956527 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_4983,GWAS_ID_4984,GWAS_ID_4985,GWAS_ID_4986 RMVar_hsa_circ_96009,RMVar_hsa_circ_111909,RMVar_hsa_circ_132657,RMVar_hsa_circ_132656,RMVar_hsa_circ_132663,RMVar_hsa_circ_78031,RMVar_hsa_circ_115021,RMVar_hsa_circ_132664,RMVar_hsa_circ_369331,RMVar_hsa_circ_132669,RMVar_hsa_circ_354932,RMVar_hsa_circ_281295 42949 RMVar_ID_42949 Human_SNP_ID_12031571 A-to-I Human chr1 - 46590320 46590320 46590320 GTCATGTGGACTCTAATACTGCTCCGGCTACTACTTCAAAGATGTAAATGTTCTGGGGTCAGTCT GTCATGTGGACTCTAATACTGCTCCGGCTACTCCTTCAAAGATGTAAATGTTCTGGGGTCAGTCT T G MKNK1 Ensembl:ENSG00000079277 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs956527 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_4983,GWAS_ID_4984,GWAS_ID_4985,GWAS_ID_4986 RMVar_hsa_circ_96009,RMVar_hsa_circ_111909,RMVar_hsa_circ_132657,RMVar_hsa_circ_132656,RMVar_hsa_circ_132663,RMVar_hsa_circ_78031,RMVar_hsa_circ_115021,RMVar_hsa_circ_132664,RMVar_hsa_circ_369331,RMVar_hsa_circ_132669,RMVar_hsa_circ_354932,RMVar_hsa_circ_281295 42950 RMVar_ID_42950 Human_SNP_ID_12031922 A-to-I Human chr1 - 46592157 46592157 46592157 CGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGTGATTCTCCTGCTTCAGTCTCCTGAGTAACT CGGCTCACTGCAACCTCCGCCTCCCGGGTTCAGGTGATTCTCCTGCTTCAGTCTCCTGAGTAACT T C MKNK1 Ensembl:ENSG00000079277 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1226203124 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96009,RMVar_hsa_circ_111909,RMVar_hsa_circ_132657,RMVar_hsa_circ_132656,RMVar_hsa_circ_132663,RMVar_hsa_circ_78031,RMVar_hsa_circ_115021,RMVar_hsa_circ_132664,RMVar_hsa_circ_369331,RMVar_hsa_circ_132669,RMVar_hsa_circ_354932,RMVar_hsa_circ_281295 42951 RMVar_ID_42951 Human_SNP_ID_12043881 A-to-I Human chr1 - 46645971 46645971 46645971 GGGGTCTCACTGTATTGTCCAGGTTGGCCTCAAACTCCTGAGCTCAAGTGATCCTCCGACCTTGG GGGGTCTCACTGTATTGTCCAGGTTGGCCTCACACTCCTGAGCTCAAGTGATCCTCCGACCTTGG T G ATPAF1 Ensembl:ENSG00000123472 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1408302461 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_355101 42952 RMVar_ID_42952 Human_SNP_ID_12045114 A-to-I Human chr1 - 46651433 46651433 46651433 ACACGTATGCTTATTGCAGCTTTATTCACAATAGCAAAGACTTGGAACCAACCCAAATGTCCAAC ACACGTATGCTTATTGCAGCTTTATTCACAATCGCAAAGACTTGGAACCAACCCAAATGTCCAAC T G ATPAF1 Ensembl:ENSG00000123472 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1244821628 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_355101 42953 RMVar_ID_42953 Human_SNP_ID_12049010 A-to-I Human chr1 - 46668084 46668084 46668084 CGAGCTCCAGGCCAACCCTTTCTACGACCGCTACCGCGACAAGATCCAGCTGCTGCGCAGGTGCG CGAGCTCCAGGCCAACCCTTTCTACGACCGCTGCCGCGACAAGATCCAGCTGCTGCGCAGGTGCG T C ATPAF1 Ensembl:ENSG00000123472 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1454713893 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_356939,Human_RBP_ID_5833066,Human_RBP_ID_8970936 Human_Splice_Rec_66391,Human_Splice_Rec_66431,Human_Splice_Rec_66447,Human_Splice_Rec_66491,Human_Splice_Rec_66529,Human_Splice_Rec_66539,Human_Splice_Rec_66557 42954 RMVar_ID_42954 Human_SNP_ID_12193986 A-to-I Human chr1 - 47266526 47266526 47266526 GACCCTGTCTCTATAAAAAAATATTTTAACTTAGCTGGGTGTGGTGGTATGTGCCTGTAGTAGTT GACCCTGTCTCTATAAAAAAATATTTTAACTTGGCTGGGTGTGGTGGTATGTGCCTGTAGTAGTT T C STIL Ensembl:ENSG00000123473 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1403307564 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1141,RMVar_hsa_circ_294130,RMVar_hsa_circ_308227,RMVar_hsa_circ_326024,RMVar_hsa_circ_345833,RMVar_hsa_circ_66711,RMVar_hsa_circ_72655,RMVar_hsa_circ_132688,RMVar_hsa_circ_271423,RMVar_hsa_circ_132685,RMVar_hsa_circ_306071,RMVar_hsa_circ_330688,RMVar_hsa_circ_100621,RMVar_hsa_circ_105308,RMVar_hsa_circ_55298,RMVar_hsa_circ_132689,RMVar_hsa_circ_132687 42955 RMVar_ID_42955 Human_SNP_ID_12194220 A-to-I Human chr1 - 47267637 47267637 47267637 TTAGATACTCGCTCTGTCGCCCTGGCTGGAGTACGGTGGCGTGATCTTGGCTCACTGCAACCTCA TTAGATACTCGCTCTGTCGCCCTGGCTGGAGTGCGGTGGCGTGATCTTGGCTCACTGCAACCTCA T C STIL Ensembl:ENSG00000123473 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1263543955 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1141,RMVar_hsa_circ_294130,RMVar_hsa_circ_308227,RMVar_hsa_circ_326024,RMVar_hsa_circ_345833,RMVar_hsa_circ_66711,RMVar_hsa_circ_72655,RMVar_hsa_circ_132688,RMVar_hsa_circ_271423,RMVar_hsa_circ_132685,RMVar_hsa_circ_306071,RMVar_hsa_circ_330688,RMVar_hsa_circ_100621,RMVar_hsa_circ_105308,RMVar_hsa_circ_55298,RMVar_hsa_circ_132689,RMVar_hsa_circ_132687 42956 RMVar_ID_42956 Human_SNP_ID_12201493 A-to-I Human chr1 - 47295414 47295414 47295414 CACCATGCCTGGCTAATTTTTGCTTTTTTAGTAGAGACGGGGTTTTACCATGTTGGCCAGGCTCG CACCATGCCTGGCTAATTTTTGCTTTTTTAGTGGAGACGGGGTTTTACCATGTTGGCCAGGCTCG T C STIL Ensembl:ENSG00000123473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1282029570 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1141,RMVar_hsa_circ_326024,RMVar_hsa_circ_66711,RMVar_hsa_circ_72655,RMVar_hsa_circ_2909,RMVar_hsa_circ_116845,RMVar_hsa_circ_306071,RMVar_hsa_circ_330688,RMVar_hsa_circ_302497,RMVar_hsa_circ_339174,RMVar_hsa_circ_338222,RMVar_hsa_circ_294508,RMVar_hsa_circ_290386,RMVar_hsa_circ_132694,RMVar_hsa_circ_132695,RMVar_hsa_circ_316718,RMVar_hsa_circ_333771,RMVar_hsa_circ_365504,RMVar_hsa_circ_349305,RMVar_hsa_circ_320877,RMVar_hsa_circ_122564,RMVar_hsa_circ_56621,RMVar_hsa_circ_132696,RMVar_hsa_circ_132698,RMVar_hsa_circ_132699,RMVar_hsa_circ_132697,RMVar_hsa_circ_132702,RMVar_hsa_circ_121738,RMVar_hsa_circ_304340,RMVar_hsa_circ_309054,RMVar_hsa_circ_283963,RMVar_hsa_circ_289488,RMVar_hsa_circ_280377,RMVar_hsa_circ_50820,RMVar_hsa_circ_132704,RMVar_hsa_circ_132706,RMVar_hsa_circ_132705,RMVar_hsa_circ_132703,RMVar_hsa_circ_313739,RMVar_hsa_circ_33152,RMVar_hsa_circ_49859,RMVar_hsa_circ_332924,RMVar_hsa_circ_366012,RMVar_hsa_circ_332113 42957 RMVar_ID_42957 Human_SNP_ID_12202337 A-to-I Human chr1 - 47299235 47299225 47299236 TCAAGTGATCCTCCCACTTCAGCCTCCTGAGTAGCTGTGATTACAGGTGCATGCCACTACACCGG TCAAGTGATCCTCCCACTTCAGCCTCCTGAG___________ACAGGTGCATGCCACTACACCGG TAATCACAGCTA T STIL Ensembl:ENSG00000123473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs967049660 Functional Loss DEL dbSNP153 32..42 33 - - - RMVar_hsa_circ_326024,RMVar_hsa_circ_66711,RMVar_hsa_circ_72655,RMVar_hsa_circ_2909,RMVar_hsa_circ_116845,RMVar_hsa_circ_306071,RMVar_hsa_circ_330688,RMVar_hsa_circ_302497,RMVar_hsa_circ_339174,RMVar_hsa_circ_294508,RMVar_hsa_circ_290386,RMVar_hsa_circ_132695,RMVar_hsa_circ_316718,RMVar_hsa_circ_365504,RMVar_hsa_circ_349305,RMVar_hsa_circ_320877,RMVar_hsa_circ_122564,RMVar_hsa_circ_56621,RMVar_hsa_circ_132696,RMVar_hsa_circ_132698,RMVar_hsa_circ_132697,RMVar_hsa_circ_132702,RMVar_hsa_circ_121738,RMVar_hsa_circ_304340,RMVar_hsa_circ_283963,RMVar_hsa_circ_289488,RMVar_hsa_circ_280377,RMVar_hsa_circ_50820,RMVar_hsa_circ_132704,RMVar_hsa_circ_132706,RMVar_hsa_circ_132705,RMVar_hsa_circ_313739,RMVar_hsa_circ_33152,RMVar_hsa_circ_332924,RMVar_hsa_circ_366012,RMVar_hsa_circ_332113,RMVar_hsa_circ_132710,RMVar_hsa_circ_276461,RMVar_hsa_circ_285928,RMVar_hsa_circ_341609,RMVar_hsa_circ_347762,RMVar_hsa_circ_284619,RMVar_hsa_circ_113852,RMVar_hsa_circ_132708,RMVar_hsa_circ_132709,RMVar_hsa_circ_132707 42958 RMVar_ID_42958 Human_SNP_ID_12204285 A-to-I Human chr1 - 47307094 47307094 47307094 CAAGCTGTAGTGGGGTGGCGTGATCTTGGCTCACTGAAACCTCTTCCCCCTGGGTTCAAGTGATT CAAGCTGTAGTGGGGTGGCGTGATCTTGGCTCTCTGAAACCTCTTCCCCCTGGGTTCAAGTGATT T A STIL Ensembl:ENSG00000123473 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs948178633 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2909,RMVar_hsa_circ_349305,RMVar_hsa_circ_304340,RMVar_hsa_circ_132706,RMVar_hsa_circ_33492,RMVar_hsa_circ_132710,RMVar_hsa_circ_341609,RMVar_hsa_circ_113852,RMVar_hsa_circ_337844,RMVar_hsa_circ_132713,RMVar_hsa_circ_289051,RMVar_hsa_circ_337260,RMVar_hsa_circ_132715,RMVar_hsa_circ_348020 42959 RMVar_ID_42959 Human_SNP_ID_12204886 A-to-I Human chr1 - 47309422 47309422 47309422 CCATCTCTTATTTGAAAATTTGTCGGTGGGCAAGGTGGCTTATGCCTGTAATCCTAGCACTTTGG CCATCTCTTATTTGAAAATTTGTCGGTGGGCATGGTGGCTTATGCCTGTAATCCTAGCACTTTGG T A STIL Ensembl:ENSG00000123473 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1478608371 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2909,RMVar_hsa_circ_349305,RMVar_hsa_circ_304340,RMVar_hsa_circ_132706,RMVar_hsa_circ_33492,RMVar_hsa_circ_132710,RMVar_hsa_circ_341609,RMVar_hsa_circ_113852,RMVar_hsa_circ_337844,RMVar_hsa_circ_132713,RMVar_hsa_circ_289051,RMVar_hsa_circ_337260,RMVar_hsa_circ_132715,RMVar_hsa_circ_348020 42960 RMVar_ID_42960 Human_SNP_ID_12219443 A-to-I Human chr1 + 47368721 47368721 47368721 GTTGCTCATGCTTGTGATCCCAGCATTTTGGGAAGCCAAAGCAAGAGGATCACTTGAGGCCAGGA GTTGCTCATGCTTGTGATCCCAGCATTTTGGGTAGCCAAAGCAAGAGGATCACTTGAGGCCAGGA A T CMPK1 Ensembl:ENSG00000162368 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1248505977 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_292288,RMVar_hsa_circ_303006,RMVar_hsa_circ_367188,RMVar_hsa_circ_132716,RMVar_hsa_circ_132717 42961 RMVar_ID_42961 Human_SNP_ID_12219967 A-to-I Human chr1 + 47370558 47370558 47370558 AGTTACTTGGGAGGCTGAGGCAGAAGAATCGCATGAACCTGGGAGGCAGAGGTTTTGGTGAGCCA AGTTACTTGGGAGGCTGAGGCAGAAGAATCGCGTGAACCTGGGAGGCAGAGGTTTTGGTGAGCCA A G CMPK1 Ensembl:ENSG00000162368 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs576225520 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_292288,RMVar_hsa_circ_303006,RMVar_hsa_circ_367188,RMVar_hsa_circ_132716,RMVar_hsa_circ_132717 42962 RMVar_ID_42962 Human_SNP_ID_12220065 A-to-I Human chr1 + 47370914 47370914 47370914 CAGAGGCGGAGGTTGCAGTGAGCCAGGATCGCACCATTGTACTCCAGCCTGGGCAACAGGGTGAG CAGAGGCGGAGGTTGCAGTGAGCCAGGATCGCGCCATTGTACTCCAGCCTGGGCAACAGGGTGAG A G CMPK1 Ensembl:ENSG00000162368 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946098659 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24766573 RMVar_hsa_circ_292288,RMVar_hsa_circ_303006,RMVar_hsa_circ_367188,RMVar_hsa_circ_132716,RMVar_hsa_circ_132717 42963 RMVar_ID_42963 Human_SNP_ID_12733277 A-to-I Human chr1 - 49571710 49571710 49571710 GACAAACATCAAAATAATAAAGGCCATATACTAAAAACTGACAACTAACATGGTACTGAAAGAGG GACAAACATCAAAATAATAAAGGCCATATACTGAAAACTGACAACTAACATGGTACTGAAAGAGG T C AGBL4 Ensembl:ENSG00000186094 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1228711316 Functional Loss SNV dbSNP153 33..33 33 - - - 42964 RMVar_ID_42964 Human_SNP_ID_12937169 A-to-I Human chr1 - 50437463 50437463 50437463 AAGTGATCACTTGAGCCCAGGAGTTCAAGGCTACAGTGAGCCATGATAGTGCGACTGCTACTCTG AAGTGATCACTTGAGCCCAGGAGTTCAAGGCTTCAGTGAGCCATGATAGTGCGACTGCTACTCTG T A FAF1 Ensembl:ENSG00000185104 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1463446950 Functional Loss SNV dbSNP153 33..33 33 - - - 42965 RMVar_ID_42965 Human_SNP_ID_12937170 A-to-I Human chr1 - 50437463 50437463 50437463 AAGTGATCACTTGAGCCCAGGAGTTCAAGGCTACAGTGAGCCATGATAGTGCGACTGCTACTCTG AAGTGATCACTTGAGCCCAGGAGTTCAAGGCTGCAGTGAGCCATGATAGTGCGACTGCTACTCTG T C FAF1 Ensembl:ENSG00000185104 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1463446950 Functional Loss SNV dbSNP153 33..33 33 - - - 42966 RMVar_ID_42966 Human_SNP_ID_12939835 A-to-I Human chr1 - 50449654 50449650 50449654 GAAAACTTGTCTCTACTAAAAATACAAAAATTAATTGGGCATGGTGGTGCATGCCTGTAGTCCCA GAAAACTTGTCTCTACTAAAAATACAAAAATT____GGGCATGGTGGTGCATGCCTGTAGTCCCA CAATT C FAF1 Ensembl:ENSG00000185104 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1445878655 Functional Loss DEL dbSNP153 33..36 33 - - - 42967 RMVar_ID_42967 Human_SNP_ID_12941157 A-to-I Human chr1 - 50455993 50455993 50455993 TCAGCTCACTGCCATCTCCGCCTCCCAGGCTCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGC TCAGCTCACTGCCATCTCCGCCTCCCAGGCTCGAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGC T C FAF1 Ensembl:ENSG00000185104 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs998977213 Functional Loss SNV dbSNP153 33..33 33 - - - 42968 RMVar_ID_42968 Human_SNP_ID_12967391 A-to-I Human chr1 - 50573871 50573871 50573871 CAACTGCCTCGGCCTCCCAAAGTGGTGAAATTACAGGCGTGAACCACTGCACCTAGGGAAGGCTT CAACTGCCTCGGCCTCCCAAAGTGGTGAAATTGCAGGCGTGAACCACTGCACCTAGGGAAGGCTT T C FAF1 Ensembl:ENSG00000185104 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1226550085 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21578,RMVar_hsa_circ_330052,RMVar_hsa_circ_372233,RMVar_hsa_circ_31875,RMVar_hsa_circ_132748,RMVar_hsa_circ_351451,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_264916,RMVar_hsa_circ_280631,RMVar_hsa_circ_351618,RMVar_hsa_circ_273095,RMVar_hsa_circ_53763,RMVar_hsa_circ_132756,RMVar_hsa_circ_132757,RMVar_hsa_circ_277159,RMVar_hsa_circ_303863,RMVar_hsa_circ_65173,RMVar_hsa_circ_132761,RMVar_hsa_circ_324407,RMVar_hsa_circ_346580,RMVar_hsa_circ_280835,RMVar_hsa_circ_290494,RMVar_hsa_circ_120153,RMVar_hsa_circ_132762,RMVar_hsa_circ_132764,RMVar_hsa_circ_132765,RMVar_hsa_circ_132763 42969 RMVar_ID_42969 Human_SNP_ID_12968200 A-to-I Human chr1 - 50576933 50576933 50576933 GCTGGGCATGGTGACTTACACCTGTAATCCCAACACTTCGAGGGGCCAAGGTGGGAGGATCGTTT GCTGGGCATGGTGACTTACACCTGTAATCCCAGCACTTCGAGGGGCCAAGGTGGGAGGATCGTTT T C FAF1 Ensembl:ENSG00000185104 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1179094991 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21578,RMVar_hsa_circ_330052,RMVar_hsa_circ_372233,RMVar_hsa_circ_31875,RMVar_hsa_circ_132748,RMVar_hsa_circ_351451,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_264916,RMVar_hsa_circ_280631,RMVar_hsa_circ_351618,RMVar_hsa_circ_273095,RMVar_hsa_circ_53763,RMVar_hsa_circ_132756,RMVar_hsa_circ_132757,RMVar_hsa_circ_277159,RMVar_hsa_circ_303863,RMVar_hsa_circ_65173,RMVar_hsa_circ_132761,RMVar_hsa_circ_324407,RMVar_hsa_circ_346580,RMVar_hsa_circ_280835,RMVar_hsa_circ_290494,RMVar_hsa_circ_120153,RMVar_hsa_circ_132762,RMVar_hsa_circ_132764,RMVar_hsa_circ_132765,RMVar_hsa_circ_132763 42970 RMVar_ID_42970 Human_SNP_ID_12983941 A-to-I Human chr1 - 50642989 50642989 50642989 CCTGTCTACAAAAATTAGCCAGGCATGATGGCAGGTGCCTGTAATCCCAGCTACTTGGGAGGCTG CCTGTCTACAAAAATTAGCCAGGCATGATGGCGGGTGCCTGTAATCCCAGCTACTTGGGAGGCTG T C FAF1 Ensembl:ENSG00000185104 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs866606449 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_372233,RMVar_hsa_circ_31875,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_53763,RMVar_hsa_circ_324407,RMVar_hsa_circ_346580,RMVar_hsa_circ_290494,RMVar_hsa_circ_120153,RMVar_hsa_circ_62423,RMVar_hsa_circ_132762,RMVar_hsa_circ_132763,RMVar_hsa_circ_322742,RMVar_hsa_circ_345239,RMVar_hsa_circ_73327,RMVar_hsa_circ_132769,RMVar_hsa_circ_266772,RMVar_hsa_circ_377068,RMVar_hsa_circ_115678,RMVar_hsa_circ_302183,RMVar_hsa_circ_132770,RMVar_hsa_circ_132771,RMVar_hsa_circ_320543 42971 RMVar_ID_42971 Human_SNP_ID_12991073 A-to-I Human chr1 - 50672901 50672901 50672901 GTTGCCCAGGCTGGTCTGGAACTCCTAAACTCAAGTGATCCACCCACCTCAGCCCCTAGAGTGCT GTTGCCCAGGCTGGTCTGGAACTCCTAAACTCGAGTGATCCACCCACCTCAGCCCCTAGAGTGCT T C FAF1 Ensembl:ENSG00000185104 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1425537191 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42972 RMVar_ID_42972 Human_SNP_ID_12995680 A-to-I Human chr1 - 50691381 50691380 50691382 AAAGTGAAGTGGACATTGTGGTGCATGCCTGCAGTCTCAGCTACTGGGGAGGCTGAGGCATGAGA AAAGTGAAGTGGACATTGTGGTGCATGCCTG__GTCTCAGCTACTGGGGAGGCTGAGGCATGAGA CTG C FAF1 Ensembl:ENSG00000185104 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1475747805 Functional Loss DEL dbSNP153 32..33 33 - - - 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 42973 RMVar_ID_42973 Human_SNP_ID_12996772 A-to-I Human chr1 - 50695151 50695151 50695151 CACCTGCCTCAACCTCCCAAAGTGCTGGGATTACAGACTTGAGCCACCGTGCCCAACCAACAATC CACCTGCCTCAACCTCCCAAAGTGCTGGGATTGCAGACTTGAGCCACCGTGCCCAACCAACAATC T C FAF1 Ensembl:ENSG00000185104 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1205703338 Functional Loss SNV dbSNP153 33..33 33 - - - 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 42974 RMVar_ID_42974 Human_SNP_ID_13006852 A-to-I Human chr1 - 50735994 50735994 50735994 AACATGTTGGCCGGGCACCGTAGCTTATGCCTATAACACCAGCACTTTGGGAGGCTGAGGTGGGA AACATGTTGGCCGGGCACCGTAGCTTATGCCTGTAACACCAGCACTTTGGGAGGCTGAGGTGGGA T C FAF1 Ensembl:ENSG00000185104 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334119698 Functional Loss SNV dbSNP153 33..33 33 - - - 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_290494,RMVar_hsa_circ_120153,RMVar_hsa_circ_62423,RMVar_hsa_circ_132762,RMVar_hsa_circ_322742,RMVar_hsa_circ_266772,RMVar_hsa_circ_377068,RMVar_hsa_circ_115678,RMVar_hsa_circ_132774,RMVar_hsa_circ_266651,RMVar_hsa_circ_132770,RMVar_hsa_circ_132771,RMVar_hsa_circ_320543,RMVar_hsa_circ_349107,RMVar_hsa_circ_374256,RMVar_hsa_circ_293283,RMVar_hsa_circ_3800,RMVar_hsa_circ_132777,RMVar_hsa_circ_132772,RMVar_hsa_circ_132773,RMVar_hsa_circ_288288,RMVar_hsa_circ_335009,RMVar_hsa_circ_352666,RMVar_hsa_circ_296205,RMVar_hsa_circ_132778 42975 RMVar_ID_42975 Human_SNP_ID_13008410 A-to-I Human chr1 - 50742198 50742198 50742198 GTGATGCTTCTACCTCAGCCTTCTAAGTAGCTAGGACTATAGATGTGCACCACGCCTGGCTAATT GTGATGCTTCTACCTCAGCCTTCTAAGTAGCTGGGACTATAGATGTGCACCACGCCTGGCTAATT T C FAF1 Ensembl:ENSG00000185104 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1367828087 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_372233,RMVar_hsa_circ_132748,RMVar_hsa_circ_342372,RMVar_hsa_circ_121195,RMVar_hsa_circ_57665,RMVar_hsa_circ_132758,RMVar_hsa_circ_132749,RMVar_hsa_circ_351618,RMVar_hsa_circ_290494,RMVar_hsa_circ_62423,RMVar_hsa_circ_322742,RMVar_hsa_circ_266772,RMVar_hsa_circ_115678,RMVar_hsa_circ_132771,RMVar_hsa_circ_320543,RMVar_hsa_circ_349107,RMVar_hsa_circ_374256,RMVar_hsa_circ_293283,RMVar_hsa_circ_3800,RMVar_hsa_circ_132777,RMVar_hsa_circ_132772,RMVar_hsa_circ_132773,RMVar_hsa_circ_288288,RMVar_hsa_circ_335009,RMVar_hsa_circ_352666,RMVar_hsa_circ_132778,RMVar_hsa_circ_132782,RMVar_hsa_circ_296031,RMVar_hsa_circ_302367,RMVar_hsa_circ_340641,RMVar_hsa_circ_292608,RMVar_hsa_circ_132780,RMVar_hsa_circ_132781,RMVar_hsa_circ_132779 42976 RMVar_ID_42976 Human_SNP_ID_13010741 A-to-I Human chr1 - 50751025 50751025 50751025 TCACTGTACATCCCCATATTAGTATAGTAAATAAGAAAAAGCATTTGACAATATTCAACACCCAT TCACTGTACATCCCCATATTAGTATAGTAAATGAGAAAAAGCATTTGACAATATTCAACACCCAT T C FAF1 Ensembl:ENSG00000185104 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1293379392 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121195,RMVar_hsa_circ_57665,RMVar_hsa_circ_132749,RMVar_hsa_circ_62423,RMVar_hsa_circ_266772,RMVar_hsa_circ_713,RMVar_hsa_circ_349107,RMVar_hsa_circ_374256,RMVar_hsa_circ_3800,RMVar_hsa_circ_132772,RMVar_hsa_circ_335009,RMVar_hsa_circ_352666,RMVar_hsa_circ_132778,RMVar_hsa_circ_296031,RMVar_hsa_circ_302367,RMVar_hsa_circ_340641,RMVar_hsa_circ_132780,RMVar_hsa_circ_132781,RMVar_hsa_circ_132779,RMVar_hsa_circ_311315 42977 RMVar_ID_42977 Human_SNP_ID_13016971 A-to-I Human chr1 - 50776076 50776076 50776076 AGTCATATTCTTCATAGTTATGGACATACTATAAACACAGTTTGACTCAAAATGAATTTTAAATC AGTCATATTCTTCATAGTTATGGACATACTATGAACACAGTTTGACTCAAAATGAATTTTAAATC T C FAF1 Ensembl:ENSG00000185104 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs756133199 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121195,RMVar_hsa_circ_57665,RMVar_hsa_circ_132749,RMVar_hsa_circ_62423,RMVar_hsa_circ_266772,RMVar_hsa_circ_713,RMVar_hsa_circ_349107,RMVar_hsa_circ_374256,RMVar_hsa_circ_3800,RMVar_hsa_circ_132772,RMVar_hsa_circ_335009,RMVar_hsa_circ_352666,RMVar_hsa_circ_132778,RMVar_hsa_circ_296031,RMVar_hsa_circ_302367,RMVar_hsa_circ_340641,RMVar_hsa_circ_132780,RMVar_hsa_circ_132779,RMVar_hsa_circ_311315 42978 RMVar_ID_42978 Human_SNP_ID_13056033 A-to-I Human chr1 - 50940535 50940535 50940535 ATGGTGTAGACCAGGCATGTTGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCAGAGGCAGAA ATGGTGTAGACCAGGCATGTTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCAGAGGCAGAA T C FAF1 Ensembl:ENSG00000185104 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1211503925 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124880,RMVar_hsa_circ_132788 42979 RMVar_ID_42979 Human_SNP_ID_13072714 A-to-I Human chr1 + 51012749 51012749 51012749 GCAGTGGCAAGAACAGGACTCACTGCAGCCTCAGCTTCCTAGGCTCAAGTAATCCTCCCGCCTCA GCAGTGGCAAGAACAGGACTCACTGCAGCCTCGGCTTCCTAGGCTCAAGTAATCCTCCCGCCTCA A G lnc-CDKN2C-1,lnc-CDKN2C-1:2 RNACentral:URS00008B231D,RNACentral:URS00008C0873 lincRNA,lincRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs575983029 Functional Loss SNV dbSNP153 33..33 33 - - - 42980 RMVar_ID_42980 Human_SNP_ID_13117179 A-to-I Human chr1 - 51208143 51208120 51208144 TTGCTCGGGCTGGTCTCGAACTCCTGGGTTCAAGTGATCCTCCTGCTTTGGATTCTCAAAGTGCT TTGCTCGGGCTGGTCTCGAACTCCTGGGTTC________________________TCAAAGTGCT AGAATCCAAAGCAGGAGGATCACTT A LINC01562 Ensembl:ENSG00000203356 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs951778221 Functional Loss DEL dbSNP153 32..55 33 - - - 42981 RMVar_ID_42981 Human_SNP_ID_13117184 A-to-I Human chr1 - 51208143 51208143 51208143 TTGCTCGGGCTGGTCTCGAACTCCTGGGTTCAAGTGATCCTCCTGCTTTGGATTCTCAAAGTGCT TTGCTCGGGCTGGTCTCGAACTCCTGGGTTCAGGTGATCCTCCTGCTTTGGATTCTCAAAGTGCT T C LINC01562 Ensembl:ENSG00000203356 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs915529718 Functional Loss SNV dbSNP153 33..33 33 - - - 42982 RMVar_ID_42982 Human_SNP_ID_13122405 A-to-I Human chr1 - 51231001 51231001 51231001 GGAGTGCAGTGGAAAGATCATAGCTCACCGCAACATCGAACTCCTGGGCTCAAGCTATCCTCCCG GGAGTGCAGTGGAAAGATCATAGCTCACCGCAGCATCGAACTCCTGGGCTCAAGCTATCCTCCCG T C LINC01562 Ensembl:ENSG00000203356 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs755439253 Functional Loss SNV dbSNP153 33..33 33 - - - 42983 RMVar_ID_42983 Human_SNP_ID_13126612 A-to-I Human chr1 + 51246511 51246510 51246511 AGGAATGCTTGAGCTCAGGAGTTGGAAGGTATAATGAGCTGTGATGGCACCATTGCACTCCAGCC AGGAATGCTTGAGCTCAGGAGTTGGAAGGTAT_ATGAGCTGTGATGGCACCATTGCACTCCAGCC TA T RNF11 Ensembl:ENSG00000123091 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1416635741 Functional Loss DEL dbSNP153 33..33 33 - - - 42984 RMVar_ID_42984 Human_SNP_ID_13126874 A-to-I Human chr1 + 51247486 51247486 51247486 GTTTTTTTTTTTTGTAAAGACAGTGTCTCATTATGTTGGCCAGGCTGGTCTTGAACTCCTGGCCC GTTTTTTTTTTTTGTAAAGACAGTGTCTCATTGTGTTGGCCAGGCTGGTCTTGAACTCCTGGCCC A G RNF11 Ensembl:ENSG00000123091 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1234183493 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11022136 42985 RMVar_ID_42985 Human_SNP_ID_13133402 A-to-I Human chr1 + 51274162 51274162 51274162 CTCTTGTTGCCCAGGCTGGAGTGCAATGGCGCAATCTCGGCTCACTGCAACCTCTGTCTCCTGGG CTCTTGTTGCCCAGGCTGGAGTGCAATGGCGCGATCTCGGCTCACTGCAACCTCTGTCTCCTGGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1217174202 Functional Loss SNV dbSNP153 33..33 33 - - - 42986 RMVar_ID_42986 Human_SNP_ID_13139550 A-to-I Human chr1 - 51299917 51299917 51299917 CCTCAGGGAACCTTTTTTCTTTTTTTAGAGACAGGGTCTTGCTATGTTGGTCAGGCTAGTCTTGA CCTCAGGGAACCTTTTTTCTTTTTTTAGAGACGGGGTCTTGCTATGTTGGTCAGGCTAGTCTTGA T C TTC39A Ensembl:ENSG00000085831 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984942228 Functional Loss SNV dbSNP153 33..33 33 - - - 42987 RMVar_ID_42987 Human_SNP_ID_13153076 A-to-I Human chr1 - 51357255 51357255 51357255 CATGTGCCTCACCCTCCCAAGTAGCTGGGATTACAGGCACCACCACCATGCCCAGCTAATTTTTG CATGTGCCTCACCCTCCCAAGTAGCTGGGATTGCAGGCACCACCACCATGCCCAGCTAATTTTTG T C EPS15 Ensembl:ENSG00000085832 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1361583052 Functional Loss SNV dbSNP153 33..33 33 - - - 42988 RMVar_ID_42988 Human_SNP_ID_13153093 A-to-I Human chr1 - 51357314 51357314 51357314 GGAGTGCAGGGGTGCATTTTCGGCTCACTGCAACCTCTGCCTCCTGGGTTCAAGTGATTCATGTG GGAGTGCAGGGGTGCATTTTCGGCTCACTGCAGCCTCTGCCTCCTGGGTTCAAGTGATTCATGTG T C EPS15 Ensembl:ENSG00000085832 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1312745697 Functional Loss SNV dbSNP153 33..33 33 - - - 42989 RMVar_ID_42989 Human_SNP_ID_13153541 A-to-I Human chr1 - 51357877 51357877 51357877 GGATTAGCCGGGCGTGGTGGTGCATGCTTGTAATTCCAGCTACTCGGGAGGCTGAGGCAAGAGAA GGATTAGCCGGGCGTGGTGGTGCATGCTTGTAGTTCCAGCTACTCGGGAGGCTGAGGCAAGAGAA T C EPS15 Ensembl:ENSG00000085832 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1199571029 Functional Loss SNV dbSNP153 33..33 33 - - - 42990 RMVar_ID_42990 Human_SNP_ID_13153815 A-to-I Human chr1 - 51358792 51358792 51358792 TGAGGTGGGAGGATCACTTAAGCCCCAGAGGCAGAGGTTGCGGGAGCTGATATAGTGCCACTGTC TGAGGTGGGAGGATCACTTAAGCCCCAGAGGCGGAGGTTGCGGGAGCTGATATAGTGCCACTGTC T C EPS15 Ensembl:ENSG00000085832 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs956694259 Functional Loss SNV dbSNP153 33..33 33 - - - 42991 RMVar_ID_42991 Human_SNP_ID_13153926 A-to-I Human chr1 - 51359344 51359344 51359344 CACCTCCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCACGCA CACCTCCCAGGTTCAAGCAATTCTCCTGCCTCGGCCTCCCAAGTAGCTGGGACTACAGGCACGCA T C EPS15 Ensembl:ENSG00000085832 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs889309016 Functional Loss SNV dbSNP153 33..33 33 - - - 42992 RMVar_ID_42992 Human_SNP_ID_13154003 A-to-I Human chr1 - 51359503 51359503 51359503 CACCGGCCTCAGCCTCTCAAAGTGTTGGGATTACAGGTGTGAGCCATCGCGCCCAGCCTTACTTA CACCGGCCTCAGCCTCTCAAAGTGTTGGGATTGCAGGTGTGAGCCATCGCGCCCAGCCTTACTTA T C EPS15 Ensembl:ENSG00000085832 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1009019462 Functional Loss SNV dbSNP153 33..33 33 - - - 42993 RMVar_ID_42993 Human_SNP_ID_13166393 A-to-I Human chr1 - 51407335 51407335 51407335 AAATTAACTGGGCATGGTGGTACCTGCCTGTAATTCCAGCTACTTGGGAGGCTGAGGCACGAGAA AAATTAACTGGGCATGGTGGTACCTGCCTGTATTTCCAGCTACTTGGGAGGCTGAGGCACGAGAA T A EPS15 Ensembl:ENSG00000085832 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1254698100 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74523,RMVar_hsa_circ_51888,RMVar_hsa_circ_281889,RMVar_hsa_circ_298597,RMVar_hsa_circ_376624,RMVar_hsa_circ_348284,RMVar_hsa_circ_296921,RMVar_hsa_circ_123591,RMVar_hsa_circ_270172,RMVar_hsa_circ_118296,RMVar_hsa_circ_132807,RMVar_hsa_circ_132809,RMVar_hsa_circ_132808,RMVar_hsa_circ_132805,RMVar_hsa_circ_132806,RMVar_hsa_circ_132804,RMVar_hsa_circ_352617,RMVar_hsa_circ_132816,RMVar_hsa_circ_91779,RMVar_hsa_circ_123941,RMVar_hsa_circ_81416,RMVar_hsa_circ_132817,RMVar_hsa_circ_132815,RMVar_hsa_circ_268388,RMVar_hsa_circ_302520,RMVar_hsa_circ_265969,RMVar_hsa_circ_132820,RMVar_hsa_circ_132824,RMVar_hsa_circ_102232,RMVar_hsa_circ_301691,RMVar_hsa_circ_324415,RMVar_hsa_circ_341535,RMVar_hsa_circ_371363,RMVar_hsa_circ_317168,RMVar_hsa_circ_294036,RMVar_hsa_circ_125081,RMVar_hsa_circ_16286,RMVar_hsa_circ_75850,RMVar_hsa_circ_132825,RMVar_hsa_circ_132822,RMVar_hsa_circ_132823,RMVar_hsa_circ_132821,RMVar_hsa_circ_54482,RMVar_hsa_circ_132818,RMVar_hsa_circ_132819,RMVar_hsa_circ_265733,RMVar_hsa_circ_322628,RMVar_hsa_circ_72936,RMVar_hsa_circ_73219,RMVar_hsa_circ_132828,RMVar_hsa_circ_281849,RMVar_hsa_circ_83642,RMVar_hsa_circ_132830,RMVar_hsa_circ_132831 42994 RMVar_ID_42994 Human_SNP_ID_13166405 A-to-I Human chr1 - 51407381 51407381 51407381 CAGCCCTGCCAACATGGCCAAACTCTGTTTCTACTAAAAGGTACAAAAATTAACTGGGCATGGTG CAGCCCTGCCAACATGGCCAAACTCTGTTTCTTCTAAAAGGTACAAAAATTAACTGGGCATGGTG T A EPS15 Ensembl:ENSG00000085832 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1186799654 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74523,RMVar_hsa_circ_51888,RMVar_hsa_circ_281889,RMVar_hsa_circ_298597,RMVar_hsa_circ_376624,RMVar_hsa_circ_348284,RMVar_hsa_circ_296921,RMVar_hsa_circ_123591,RMVar_hsa_circ_270172,RMVar_hsa_circ_118296,RMVar_hsa_circ_132807,RMVar_hsa_circ_132809,RMVar_hsa_circ_132808,RMVar_hsa_circ_132805,RMVar_hsa_circ_132806,RMVar_hsa_circ_132804,RMVar_hsa_circ_352617,RMVar_hsa_circ_132816,RMVar_hsa_circ_91779,RMVar_hsa_circ_123941,RMVar_hsa_circ_81416,RMVar_hsa_circ_132817,RMVar_hsa_circ_132815,RMVar_hsa_circ_268388,RMVar_hsa_circ_302520,RMVar_hsa_circ_265969,RMVar_hsa_circ_132820,RMVar_hsa_circ_132824,RMVar_hsa_circ_102232,RMVar_hsa_circ_301691,RMVar_hsa_circ_324415,RMVar_hsa_circ_341535,RMVar_hsa_circ_371363,RMVar_hsa_circ_317168,RMVar_hsa_circ_294036,RMVar_hsa_circ_125081,RMVar_hsa_circ_16286,RMVar_hsa_circ_75850,RMVar_hsa_circ_132825,RMVar_hsa_circ_132822,RMVar_hsa_circ_132823,RMVar_hsa_circ_132821,RMVar_hsa_circ_54482,RMVar_hsa_circ_132818,RMVar_hsa_circ_132819,RMVar_hsa_circ_265733,RMVar_hsa_circ_322628,RMVar_hsa_circ_72936,RMVar_hsa_circ_73219,RMVar_hsa_circ_132828,RMVar_hsa_circ_281849,RMVar_hsa_circ_83642,RMVar_hsa_circ_132830,RMVar_hsa_circ_132831 42995 RMVar_ID_42995 Human_SNP_ID_13178679 A-to-I Human chr1 - 51458654 51458654 51458654 CAGCTCACTGCAGCCTCGGCCTCCTGGATTCAAGTTATTCTTCCACCTCAGCCTCCTGAGGAGCT CAGCTCACTGCAGCCTCGGCCTCCTGGATTCAGGTTATTCTTCCACCTCAGCCTCCTGAGGAGCT T C EPS15 Ensembl:ENSG00000085832 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1291561119 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24766819 Human_Splice_Rec_69074,Human_Splice_Rec_69082 RMVar_hsa_circ_376624,RMVar_hsa_circ_118296,RMVar_hsa_circ_132804,RMVar_hsa_circ_265969,RMVar_hsa_circ_132820,RMVar_hsa_circ_102232,RMVar_hsa_circ_371363,RMVar_hsa_circ_294036,RMVar_hsa_circ_125081,RMVar_hsa_circ_132821,RMVar_hsa_circ_132818,RMVar_hsa_circ_132819,RMVar_hsa_circ_83642,RMVar_hsa_circ_132831,RMVar_hsa_circ_11951,RMVar_hsa_circ_42490,RMVar_hsa_circ_28478,RMVar_hsa_circ_377444,RMVar_hsa_circ_285330,RMVar_hsa_circ_132838,RMVar_hsa_circ_25619,RMVar_hsa_circ_132840,RMVar_hsa_circ_315535,RMVar_hsa_circ_305440 42996 RMVar_ID_42996 Human_SNP_ID_13189234 A-to-I Human chr1 - 51500862 51500862 51500862 CTCCTCCCTCAGCCTCCCAAGTAGCTGGGATTACAGGTGTGTGCCACCATGCCCTGCTAATATTT CTCCTCCCTCAGCCTCCCAAGTAGCTGGGATTGCAGGTGTGTGCCACCATGCCCTGCTAATATTT T C EPS15 Ensembl:ENSG00000085832 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs975438190 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117028,RMVar_hsa_circ_132847,RMVar_hsa_circ_132849 42997 RMVar_ID_42997 Human_SNP_ID_13189836 A-to-I Human chr1 - 51503401 51503401 51503401 AAACTCCCGACTTTAGGTAATCCACCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAC AAACTCCCGACTTTAGGTAATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAC T C EPS15 Ensembl:ENSG00000085832 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs889612884 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117028,RMVar_hsa_circ_132847,RMVar_hsa_circ_132849 42998 RMVar_ID_42998 Human_SNP_ID_13231747 A-to-I Human chr1 + 51684137 51684137 51684137 GTGATCTTTCCACCTCAGAGTCCTGAGTAGCTAGGACTGCAGGCACTCACTCCCATGCCCAACTA GTGATCTTTCCACCTCAGAGTCCTGAGTAGCTGGGACTGCAGGCACTCACTCCCATGCCCAACTA A G OSBPL9 Ensembl:ENSG00000117859 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs543593898 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_62454,RMVar_hsa_circ_378949,RMVar_hsa_circ_132853,RMVar_hsa_circ_86879,RMVar_hsa_circ_333524,RMVar_hsa_circ_132852 42999 RMVar_ID_42999 Human_SNP_ID_13247020 A-to-I Human chr1 + 51752501 51752501 51752501 GTTTGTTTATCTCTTTATTGACTGTCTACCCTAGAGTACAATCTTGGTGAGGAATTTGCTCGTCT GTTTGTTTATCTCTTTATTGACTGTCTACCCTGGAGTACAATCTTGGTGAGGAATTTGCTCGTCT A G OSBPL9 Ensembl:ENSG00000117859 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1354975863 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3316344,Human_RBP_ID_22707990 RMVar_hsa_circ_132853,RMVar_hsa_circ_86879,RMVar_hsa_circ_356575,RMVar_hsa_circ_364066,RMVar_hsa_circ_102747,RMVar_hsa_circ_67836,RMVar_hsa_circ_15550,RMVar_hsa_circ_65077,RMVar_hsa_circ_132855,RMVar_hsa_circ_34789,RMVar_hsa_circ_280792,RMVar_hsa_circ_301273,RMVar_hsa_circ_273705,RMVar_hsa_circ_39352,RMVar_hsa_circ_62476,RMVar_hsa_circ_32843,RMVar_hsa_circ_132856,RMVar_hsa_circ_132857,RMVar_hsa_circ_132858,RMVar_hsa_circ_313159,RMVar_hsa_circ_317627,RMVar_hsa_circ_127458,RMVar_hsa_circ_22885,RMVar_hsa_circ_72256,RMVar_hsa_circ_301237,RMVar_hsa_circ_132859,RMVar_hsa_circ_277874,RMVar_hsa_circ_278918,RMVar_hsa_circ_132860,RMVar_hsa_circ_291943,RMVar_hsa_circ_272051,RMVar_hsa_circ_132862,RMVar_hsa_circ_132863,RMVar_hsa_circ_132861 43000 RMVar_ID_43000 Human_SNP_ID_13247032 A-to-I Human chr1 + 51752544 51752544 51752544 TTGGTGAGGAATTTGCTCGTCTTACCACTTGTATTAGTCTGCATGGGCTGCCATAACAAAATACC TTGGTGAGGAATTTGCTCGTCTTACCACTTGTGTTAGTCTGCATGGGCTGCCATAACAAAATACC A G OSBPL9 Ensembl:ENSG00000117859 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1477907408 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22707990 Human_Splice_Rec_69460 RMVar_hsa_circ_132853,RMVar_hsa_circ_86879,RMVar_hsa_circ_356575,RMVar_hsa_circ_364066,RMVar_hsa_circ_102747,RMVar_hsa_circ_67836,RMVar_hsa_circ_15550,RMVar_hsa_circ_65077,RMVar_hsa_circ_132855,RMVar_hsa_circ_34789,RMVar_hsa_circ_280792,RMVar_hsa_circ_301273,RMVar_hsa_circ_273705,RMVar_hsa_circ_39352,RMVar_hsa_circ_62476,RMVar_hsa_circ_32843,RMVar_hsa_circ_132856,RMVar_hsa_circ_132857,RMVar_hsa_circ_132858,RMVar_hsa_circ_313159,RMVar_hsa_circ_317627,RMVar_hsa_circ_127458,RMVar_hsa_circ_22885,RMVar_hsa_circ_72256,RMVar_hsa_circ_301237,RMVar_hsa_circ_132859,RMVar_hsa_circ_277874,RMVar_hsa_circ_278918,RMVar_hsa_circ_132860,RMVar_hsa_circ_291943,RMVar_hsa_circ_272051,RMVar_hsa_circ_132862,RMVar_hsa_circ_132863,RMVar_hsa_circ_132861 43001 RMVar_ID_43001 Human_SNP_ID_13247033 A-to-I Human chr1 + 51752547 51752547 51752547 GTGAGGAATTTGCTCGTCTTACCACTTGTATTAGTCTGCATGGGCTGCCATAACAAAATACCATA GTGAGGAATTTGCTCGTCTTACCACTTGTATTCGTCTGCATGGGCTGCCATAACAAAATACCATA A C OSBPL9 Ensembl:ENSG00000117859 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1233961397 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22707990 Human_Splice_Rec_69460 RMVar_hsa_circ_132853,RMVar_hsa_circ_86879,RMVar_hsa_circ_356575,RMVar_hsa_circ_364066,RMVar_hsa_circ_102747,RMVar_hsa_circ_67836,RMVar_hsa_circ_15550,RMVar_hsa_circ_65077,RMVar_hsa_circ_132855,RMVar_hsa_circ_34789,RMVar_hsa_circ_280792,RMVar_hsa_circ_301273,RMVar_hsa_circ_273705,RMVar_hsa_circ_39352,RMVar_hsa_circ_62476,RMVar_hsa_circ_32843,RMVar_hsa_circ_132856,RMVar_hsa_circ_132857,RMVar_hsa_circ_132858,RMVar_hsa_circ_313159,RMVar_hsa_circ_317627,RMVar_hsa_circ_127458,RMVar_hsa_circ_22885,RMVar_hsa_circ_72256,RMVar_hsa_circ_301237,RMVar_hsa_circ_132859,RMVar_hsa_circ_277874,RMVar_hsa_circ_278918,RMVar_hsa_circ_132860,RMVar_hsa_circ_291943,RMVar_hsa_circ_272051,RMVar_hsa_circ_132862,RMVar_hsa_circ_132863,RMVar_hsa_circ_132861 43002 RMVar_ID_43002 Human_SNP_ID_13247593 A-to-I Human chr1 + 51755216 51755216 51755216 ATACAAGTGGTAAGATGAGCAAAGTCCTCACCAAGATTGTACTCTAGGGTAGACGGCCAATAAAG ATACAAGTGGTAAGATGAGCAAAGTCCTCACCGAGATTGTACTCTAGGGTAGACGGCCAATAAAG A G OSBPL9 Ensembl:ENSG00000117859 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1246932445 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9527242,Human_RBP_ID_22707991,Human_RBP_ID_22865551,Human_RBP_ID_24766880 RMVar_hsa_circ_132853,RMVar_hsa_circ_86879,RMVar_hsa_circ_356575,RMVar_hsa_circ_364066,RMVar_hsa_circ_102747,RMVar_hsa_circ_67836,RMVar_hsa_circ_15550,RMVar_hsa_circ_65077,RMVar_hsa_circ_132855,RMVar_hsa_circ_34789,RMVar_hsa_circ_280792,RMVar_hsa_circ_301273,RMVar_hsa_circ_273705,RMVar_hsa_circ_39352,RMVar_hsa_circ_62476,RMVar_hsa_circ_132856,RMVar_hsa_circ_132857,RMVar_hsa_circ_132858,RMVar_hsa_circ_313159,RMVar_hsa_circ_317627,RMVar_hsa_circ_127458,RMVar_hsa_circ_22885,RMVar_hsa_circ_72256,RMVar_hsa_circ_301237,RMVar_hsa_circ_132859,RMVar_hsa_circ_277874,RMVar_hsa_circ_278918,RMVar_hsa_circ_132860,RMVar_hsa_circ_291943,RMVar_hsa_circ_272051,RMVar_hsa_circ_132862,RMVar_hsa_circ_132863,RMVar_hsa_circ_132861 43003 RMVar_ID_43003 Human_SNP_ID_13247595 A-to-I Human chr1 + 51755224 51755224 51755224 GGTAAGATGAGCAAAGTCCTCACCAAGATTGTACTCTAGGGTAGACGGCCAATAAAGAGATAAAT GGTAAGATGAGCAAAGTCCTCACCAAGATTGTTCTCTAGGGTAGACGGCCAATAAAGAGATAAAT A T OSBPL9 Ensembl:ENSG00000117859 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1313293148 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_96510,Human_RBP_ID_9527242,Human_RBP_ID_11024551,Human_RBP_ID_22707991,Human_RBP_ID_22865551,Human_RBP_ID_24766880 RMVar_hsa_circ_132853,RMVar_hsa_circ_86879,RMVar_hsa_circ_356575,RMVar_hsa_circ_364066,RMVar_hsa_circ_102747,RMVar_hsa_circ_67836,RMVar_hsa_circ_15550,RMVar_hsa_circ_65077,RMVar_hsa_circ_132855,RMVar_hsa_circ_34789,RMVar_hsa_circ_280792,RMVar_hsa_circ_301273,RMVar_hsa_circ_273705,RMVar_hsa_circ_39352,RMVar_hsa_circ_62476,RMVar_hsa_circ_132856,RMVar_hsa_circ_132857,RMVar_hsa_circ_132858,RMVar_hsa_circ_313159,RMVar_hsa_circ_317627,RMVar_hsa_circ_127458,RMVar_hsa_circ_22885,RMVar_hsa_circ_72256,RMVar_hsa_circ_301237,RMVar_hsa_circ_132859,RMVar_hsa_circ_277874,RMVar_hsa_circ_278918,RMVar_hsa_circ_132860,RMVar_hsa_circ_291943,RMVar_hsa_circ_272051,RMVar_hsa_circ_132862,RMVar_hsa_circ_132863,RMVar_hsa_circ_132861 43004 RMVar_ID_43004 Human_SNP_ID_13250137 A-to-I Human chr1 + 51767215 51767215 51767215 CAGGAGTTTGAGACCAGCTTGGGCAACATGGTAAAACCCTGTCTCTAAAAAAATACAAAAATTAG CAGGAGTTTGAGACCAGCTTGGGCAACATGGTGAAACCCTGTCTCTAAAAAAATACAAAAATTAG A G OSBPL9 Ensembl:ENSG00000117859 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1216213226 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14823,RMVar_hsa_circ_15550,RMVar_hsa_circ_65077,RMVar_hsa_circ_34789,RMVar_hsa_circ_273705,RMVar_hsa_circ_62476,RMVar_hsa_circ_132858,RMVar_hsa_circ_317627,RMVar_hsa_circ_22885,RMVar_hsa_circ_301237,RMVar_hsa_circ_132860,RMVar_hsa_circ_272051,RMVar_hsa_circ_132861,RMVar_hsa_circ_297409,RMVar_hsa_circ_316898,RMVar_hsa_circ_293784,RMVar_hsa_circ_132866,RMVar_hsa_circ_32520,RMVar_hsa_circ_314216,RMVar_hsa_circ_100105,RMVar_hsa_circ_13113,RMVar_hsa_circ_132868 43005 RMVar_ID_43005 Human_SNP_ID_13258829 A-to-I Human chr1 - 51803461 51803457 51803461 CTTTTTTTTTTTTTTTTTTGAGACAGATACTCACTCCATCACCCAGACTGGAATGCAGTGGTGTG CTTTTTTTTTTTTTTTTTTGAGACAGATACTC____CATCACCCAGACTGGAATGCAGTGGTGTG GGAGT G NRDC Ensembl:ENSG00000078618 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs755048647 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_5837904 RMVar_hsa_circ_250,RMVar_hsa_circ_34023,RMVar_hsa_circ_371730,RMVar_hsa_circ_67541,RMVar_hsa_circ_132877,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,RMVar_hsa_circ_23582,RMVar_hsa_circ_347031,RMVar_hsa_circ_12321,RMVar_hsa_circ_11979,RMVar_hsa_circ_50958,RMVar_hsa_circ_132882,RMVar_hsa_circ_132883,RMVar_hsa_circ_315189,RMVar_hsa_circ_13524,RMVar_hsa_circ_132885,RMVar_hsa_circ_132886,RMVar_hsa_circ_132887,RMVar_hsa_circ_132884 43006 RMVar_ID_43006 Human_SNP_ID_13265417 A-to-I Human chr1 - 51833846 51833846 51833846 CTTTGGGAGGCTGAGGTAGAAGGCTCGCTTAAAGCCAGGAGTTTGAGACCAGCTTGGGCAAAATA CTTTGGGAGGCTGAGGTAGAAGGCTCGCTTAAGGCCAGGAGTTTGAGACCAGCTTGGGCAAAATA T C NRDC Ensembl:ENSG00000078618 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs566113704 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34023,RMVar_hsa_circ_103767,RMVar_hsa_circ_78166,RMVar_hsa_circ_132879,RMVar_hsa_circ_132880,RMVar_hsa_circ_11979,RMVar_hsa_circ_132887,RMVar_hsa_circ_303176,RMVar_hsa_circ_132888,RMVar_hsa_circ_294881,RMVar_hsa_circ_343054,RMVar_hsa_circ_356702,RMVar_hsa_circ_132894,RMVar_hsa_circ_347463,RMVar_hsa_circ_276938,RMVar_hsa_circ_132899,RMVar_hsa_circ_62314,RMVar_hsa_circ_280188,RMVar_hsa_circ_132902,RMVar_hsa_circ_41692,RMVar_hsa_circ_291210,RMVar_hsa_circ_62713,RMVar_hsa_circ_16605,RMVar_hsa_circ_5550,RMVar_hsa_circ_132903,RMVar_hsa_circ_60868,RMVar_hsa_circ_274550,RMVar_hsa_circ_359022,RMVar_hsa_circ_362060,RMVar_hsa_circ_132907,RMVar_hsa_circ_98685,RMVar_hsa_circ_121225,RMVar_hsa_circ_281263,RMVar_hsa_circ_132908,RMVar_hsa_circ_354092,RMVar_hsa_circ_124991,RMVar_hsa_circ_108297,RMVar_hsa_circ_132910,RMVar_hsa_circ_132912,RMVar_hsa_circ_132913,RMVar_hsa_circ_132911,RMVar_hsa_circ_132909 43007 RMVar_ID_43007 Human_SNP_ID_13275813 A-to-I Human chr1 - 51874005 51874005 51874005 TGGAGGTGGTGGTGGGGGCAGGTGTCTCACCAAGTTGCCCAGGCTGGTCTCGAACTCCTGACCTC TGGAGGTGGTGGTGGGGGCAGGTGTCTCACCAGGTTGCCCAGGCTGGTCTCGAACTCCTGACCTC T C NRDC Ensembl:ENSG00000078618 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1336084127 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121225,RMVar_hsa_circ_132913 43008 RMVar_ID_43008 Human_SNP_ID_13275941 A-to-I Human chr1 - 51874487 51874487 51874487 CTTCCACCTCAGGCTCTCCAGTAGCTGGGACTACAGGCACGTGCCATCATGCCCAGCTAAGCTTT CTTCCACCTCAGGCTCTCCAGTAGCTGGGACTCCAGGCACGTGCCATCATGCCCAGCTAAGCTTT T G NRDC Ensembl:ENSG00000078618 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1439784005 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121225,RMVar_hsa_circ_132913 43009 RMVar_ID_43009 Human_SNP_ID_13314432 A-to-I Human chr1 - 52038052 52038052 52038052 GTGGTGGCACACACCTGTTGTTCCTGCTACTCAGGAGTCTGAGGTGGGAGGATTGCTTGAGCCTG GTGGTGGCACACACCTGTTGTTCCTGCTACTCCGGAGTCTGAGGTGGGAGGATTGCTTGAGCCTG T G TXNDC12 Ensembl:ENSG00000117862 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1056013950 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117611,RMVar_hsa_circ_132921 43010 RMVar_ID_43010 Human_SNP_ID_13315214 A-to-I Human chr1 - 52041270 52041270 52041270 GGAGTGCAGTGGCACGATCTCGGCTCACTGCAAGCTCCACCTCCTGGGCTCACGCCATTCTCCTG GGAGTGCAGTGGCACGATCTCGGCTCACTGCAGGCTCCACCTCCTGGGCTCACGCCATTCTCCTG T C TXNDC12 Ensembl:ENSG00000117862 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1453763566 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117611,RMVar_hsa_circ_132921 43011 RMVar_ID_43011 Human_SNP_ID_13320189 A-to-I Human chr1 + 52062030 52062030 52062030 GCAATCTCAGCTCACTGCAATCTCCGCCTCCCAGGTTCATGTCATTCTCCTGCCTCAGCCTCCCA GCAATCTCAGCTCACTGCAATCTCCGCCTCCCGGGTTCATGTCATTCTCCTGCCTCAGCCTCCCA A G BTF3L4 Ensembl:ENSG00000134717 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1356991163 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_132923,RMVar_hsa_circ_86308 43012 RMVar_ID_43012 Human_SNP_ID_13321227 A-to-I Human chr1 + 52066217 52066217 52066217 ATGATTCCATTTGTTTTTTTGTTTTTTAAGACAGAATCTCACTCTGTCACCCAGGCTAGAGTGCA ATGATTCCATTTGTTTTTTTGTTTTTTAAGACGGAATCTCACTCTGTCACCCAGGCTAGAGTGCA A G BTF3L4 Ensembl:ENSG00000134717 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs998257944 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11026340 RMVar_hsa_circ_122798,RMVar_hsa_circ_132924 43013 RMVar_ID_43013 Human_SNP_ID_13321233 A-to-I Human chr1 + 52066242 52066242 52066242 TTAAGACAGAATCTCACTCTGTCACCCAGGCTAGAGTGCAGTGGTGTGATCTCTGCTCACTGCAA TTAAGACAGAATCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGTGTGATCTCTGCTCACTGCAA A G BTF3L4 Ensembl:ENSG00000134717 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1268453548 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_221997 RMVar_hsa_circ_122798,RMVar_hsa_circ_132924 43014 RMVar_ID_43014 Human_SNP_ID_13321458 A-to-I Human chr1 + 52066907 52066907 52066907 TGGTATCACCTCACAATTTTAAATAGGTGACTAATGTACATGTGCTATAAAACAAGAATCAGAAA TGGTATCACCTCACAATTTTAAATAGGTGACTGATGTACATGTGCTATAAAACAAGAATCAGAAA A G BTF3L4 Ensembl:ENSG00000134717 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1332811959 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9527664 RMVar_hsa_circ_122798,RMVar_hsa_circ_132924 43015 RMVar_ID_43015 Human_SNP_ID_13322130 A-to-I Human chr1 + 52070015 52070015 52070015 AAAGCAGGTGGATCACCTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGGTACAACACTGT AAAGCAGGTGGATCACCTGAGGTCAGGAGTTCCAGACCAGCCTGGCCAACATGGTACAACACTGT A C BTF3L4 Ensembl:ENSG00000134717 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs922639551 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122798,RMVar_hsa_circ_132924 43016 RMVar_ID_43016 Human_SNP_ID_13322348 A-to-I Human chr1 + 52070777 52070777 52070777 CTCATGCCTCAGCCTCCTGAGTGGCTGGGATTATAGGCGCACCACCACATCTGGCTAATTTTTAT CTCATGCCTCAGCCTCCTGAGTGGCTGGGATTGTAGGCGCACCACCACATCTGGCTAATTTTTAT A G BTF3L4 Ensembl:ENSG00000134717 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs953959141 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122798,RMVar_hsa_circ_132924 43017 RMVar_ID_43017 Human_SNP_ID_13322358 A-to-I Human chr1 + 52070819 52070819 52070819 CACCACATCTGGCTAATTTTTATATTTTTAGTAGAGACGGGGTTTCACCACATTGGCCAGGCTCG CACCACATCTGGCTAATTTTTATATTTTTAGTGGAGACGGGGTTTCACCACATTGGCCAGGCTCG A G BTF3L4 Ensembl:ENSG00000134717 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs991719736 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122798,RMVar_hsa_circ_132924 43018 RMVar_ID_43018 Human_SNP_ID_13322364 A-to-I Human chr1 + 52070838 52070838 52070838 TTATATTTTTAGTAGAGACGGGGTTTCACCACATTGGCCAGGCTCGTCTCAAACTCCTGACCTCA TTATATTTTTAGTAGAGACGGGGTTTCACCACGTTGGCCAGGCTCGTCTCAAACTCCTGACCTCA A G BTF3L4 Ensembl:ENSG00000134717 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs147223571 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122798,RMVar_hsa_circ_132924 43019 RMVar_ID_43019 Human_SNP_ID_13322905 A-to-I Human chr1 + 52072799 52072799 52072799 AAATATATTGCCGGATGAGTGCAGTGGTTCACACTTGTAATCCTAGCACTTTGGGAGGCTGAGGT AAATATATTGCCGGATGAGTGCAGTGGTTCACGCTTGTAATCCTAGCACTTTGGGAGGCTGAGGT A G BTF3L4 Ensembl:ENSG00000134717 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1217310152 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122798,RMVar_hsa_circ_132924 43020 RMVar_ID_43020 Human_SNP_ID_13323368 A-to-I Human chr1 + 52074235 52074235 52074235 GTTTTTTGTTTTTTGAGATAGAGTCTCACTCTATGCCCAGGCTGGAGTGCAGTGGCACAGTCTTG GTTTTTTGTTTTTTGAGATAGAGTCTCACTCTCTGCCCAGGCTGGAGTGCAGTGGCACAGTCTTG A C BTF3L4 Ensembl:ENSG00000134717 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs77641918 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122798,RMVar_hsa_circ_132924 43021 RMVar_ID_43021 Human_SNP_ID_13323369 A-to-I Human chr1 + 52074235 52074235 52074235 GTTTTTTGTTTTTTGAGATAGAGTCTCACTCTATGCCCAGGCTGGAGTGCAGTGGCACAGTCTTG GTTTTTTGTTTTTTGAGATAGAGTCTCACTCTGTGCCCAGGCTGGAGTGCAGTGGCACAGTCTTG A G BTF3L4 Ensembl:ENSG00000134717 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs77641918 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122798,RMVar_hsa_circ_132924 43022 RMVar_ID_43022 Human_SNP_ID_13323372 A-to-I Human chr1 + 52074261 52074261 52074261 CACTCTATGCCCAGGCTGGAGTGCAGTGGCACAGTCTTGGCTCACTGCAACCTCTGCTTCCCAGG CACTCTATGCCCAGGCTGGAGTGCAGTGGCACGGTCTTGGCTCACTGCAACCTCTGCTTCCCAGG A G BTF3L4 Ensembl:ENSG00000134717 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1169836436 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122798,RMVar_hsa_circ_132924 43023 RMVar_ID_43023 Human_SNP_ID_13323378 A-to-I Human chr1 + 52074297 52074297 52074297 TTGGCTCACTGCAACCTCTGCTTCCCAGGTTCAAGCGATTCTCGTGCCTCAAACTCCCAAGTAGT TTGGCTCACTGCAACCTCTGCTTCCCAGGTTCGAGCGATTCTCGTGCCTCAAACTCCCAAGTAGT A G BTF3L4 Ensembl:ENSG00000134717 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs928954466 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122798,RMVar_hsa_circ_132924 43024 RMVar_ID_43024 Human_SNP_ID_13323390 A-to-I Human chr1 + 52074330 52074330 52074330 AGCGATTCTCGTGCCTCAAACTCCCAAGTAGTAGCCGGGATTACAGGTGTGTGCCACCACAACCA AGCGATTCTCGTGCCTCAAACTCCCAAGTAGTTGCCGGGATTACAGGTGTGTGCCACCACAACCA A T BTF3L4 Ensembl:ENSG00000134717 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1394062132 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5838456,Human_RBP_ID_11026538 RMVar_hsa_circ_122798,RMVar_hsa_circ_132924 43025 RMVar_ID_43025 Human_SNP_ID_13323538 A-to-I Human chr1 + 52074940 52074940 52074940 ACCATGCCTGGCTACTTTTTAGAATTATTTGTAGAGATGAGGTCTCCCTATGTTGCCCAGGCTGG ACCATGCCTGGCTACTTTTTAGAATTATTTGTGGAGATGAGGTCTCCCTATGTTGCCCAGGCTGG A G BTF3L4 Ensembl:ENSG00000134717 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1447599733 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5838462 RMVar_hsa_circ_122798,RMVar_hsa_circ_132924 43026 RMVar_ID_43026 Human_SNP_ID_13323885 A-to-I Human chr1 + 52076230 52076230 52076230 CCCAGGAGGTGCAGGTTGCGTTGAGCAGAGATAGCACCACTGCATTCCAGCCTGGGTGACAGAGC CCCAGGAGGTGCAGGTTGCGTTGAGCAGAGATCGCACCACTGCATTCCAGCCTGGGTGACAGAGC A C BTF3L4 Ensembl:ENSG00000134717 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1440599466 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24767009 RMVar_hsa_circ_122798,RMVar_hsa_circ_132924 43027 RMVar_ID_43027 Human_SNP_ID_13323886 A-to-I Human chr1 + 52076230 52076230 52076230 CCCAGGAGGTGCAGGTTGCGTTGAGCAGAGATAGCACCACTGCATTCCAGCCTGGGTGACAGAGC CCCAGGAGGTGCAGGTTGCGTTGAGCAGAGATGGCACCACTGCATTCCAGCCTGGGTGACAGAGC A G BTF3L4 Ensembl:ENSG00000134717 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1440599466 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24767009 RMVar_hsa_circ_122798,RMVar_hsa_circ_132924 43028 RMVar_ID_43028 Human_SNP_ID_13324062 A-to-I Human chr1 + 52076894 52076894 52076894 TGTTTTACCCTATTAAGCTGTAAGAAGAGGCTAGGTGTGGTGACTTGTGTTTGTAATCCCAGCAC TGTTTTACCCTATTAAGCTGTAAGAAGAGGCTGGGTGTGGTGACTTGTGTTTGTAATCCCAGCAC A G BTF3L4 Ensembl:ENSG00000134717 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs376780842 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122798,RMVar_hsa_circ_132924 43029 RMVar_ID_43029 Human_SNP_ID_13324090 A-to-I Human chr1 + 52077021 52077021 52077021 TGACACCGTGTCTCTAAAGAAAATAAAAAATTAGCCAGGCATGGTGGCACATGCCTGTAGTCCTA TGACACCGTGTCTCTAAAGAAAATAAAAAATTGGCCAGGCATGGTGGCACATGCCTGTAGTCCTA A G BTF3L4 Ensembl:ENSG00000134717 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1237821883 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122798,RMVar_hsa_circ_132924 43030 RMVar_ID_43030 Human_SNP_ID_13324095 A-to-I Human chr1 + 52077053 52077053 52077053 AGCCAGGCATGGTGGCACATGCCTGTAGTCCTACCAACCTAGGAGGCTGAGGCAGAAGGATCCCT AGCCAGGCATGGTGGCACATGCCTGTAGTCCTGCCAACCTAGGAGGCTGAGGCAGAAGGATCCCT A G BTF3L4 Ensembl:ENSG00000134717 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1318167763 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122798,RMVar_hsa_circ_132924 43031 RMVar_ID_43031 Human_SNP_ID_13324179 A-to-I Human chr1 + 52077457 52077457 52077457 CCAGCTACTTGGGAGGATGAGGCAGTGGAATCACTTGAACTCGGGAAGCAGATGTTGCAGTGAGC CCAGCTACTTGGGAGGATGAGGCAGTGGAATCGCTTGAACTCGGGAAGCAGATGTTGCAGTGAGC A G BTF3L4 Ensembl:ENSG00000134717 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1324392922 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11026574 RMVar_hsa_circ_122798,RMVar_hsa_circ_132924 43032 RMVar_ID_43032 Human_SNP_ID_13324347 A-to-I Human chr1 + 52078192 52078192 52078192 CTCCCACCTCAGCCTCCTGAGTAGCTAAGACTATAGACATGTACCACCATGCCACCTGGATTGCT CTCCCACCTCAGCCTCCTGAGTAGCTAAGACTGTAGACATGTACCACCATGCCACCTGGATTGCT A G BTF3L4 Ensembl:ENSG00000134717 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1310731059 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11026591 RMVar_hsa_circ_122798,RMVar_hsa_circ_132924 43033 RMVar_ID_43033 Human_SNP_ID_13325027 A-to-I Human chr1 + 52080627 52080627 52080627 GCGATTTCGGCTTACTGCAACCTATGTCTCCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTG GCGATTTCGGCTTACTGCAACCTATGTCTCCCTGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTG A T BTF3L4 Ensembl:ENSG00000134717 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1436457539 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122798,RMVar_hsa_circ_132924 43034 RMVar_ID_43034 Human_SNP_ID_13325265 A-to-I Human chr1 + 52081578 52081578 52081578 ATTTCACATCCACTGTCATCCTTCTCGAGCCCAGATTTCACCCACTTTAACATTTAACTTTTTAA ATTTCACATCCACTGTCATCCTTCTCGAGCCCGGATTTCACCCACTTTAACATTTAACTTTTTAA A G BTF3L4 Ensembl:ENSG00000134717 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs3015308 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21910053 RMVar_hsa_circ_122798,RMVar_hsa_circ_132924 43035 RMVar_ID_43035 Human_SNP_ID_13325939 A-to-I Human chr1 + 52084621 52084621 52084621 CAAGACCAGCCTGGGCAACATGGTGAGACCCTATCTGTACAAAAAATACAAAAATTAGCCAGGTG CAAGACCAGCCTGGGCAACATGGTGAGACCCTGTCTGTACAAAAAATACAAAAATTAGCCAGGTG A G BTF3L4 Ensembl:ENSG00000134717 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs938900640 Functional Loss SNV dbSNP153 33..33 33 - - - 43036 RMVar_ID_43036 Human_SNP_ID_13326090 A-to-I Human chr1 + 52085118 52085118 52085118 TCTTGGCTCACTGCAACCTCCACCTGCCGGGTACAAGCAATTATCTGCCTCAGCCTCCCAAGTTA TCTTGGCTCACTGCAACCTCCACCTGCCGGGTGCAAGCAATTATCTGCCTCAGCCTCCCAAGTTA A G BTF3L4 Ensembl:ENSG00000134717 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1315115539 Functional Loss SNV dbSNP153 33..33 33 - - - 43037 RMVar_ID_43037 Human_SNP_ID_13326115 A-to-I Human chr1 + 52085204 52085204 52085204 CACTGCGCCTGGCTAATTTTTATATTTTTAGTAGAGACAGGGTTTCACCGTCTTGGCCCGGCTGG CACTGCGCCTGGCTAATTTTTATATTTTTAGTGGAGACAGGGTTTCACCGTCTTGGCCCGGCTGG A G BTF3L4 Ensembl:ENSG00000134717 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs960297349 Functional Loss SNV dbSNP153 33..33 33 - - - 43038 RMVar_ID_43038 Human_SNP_ID_13326250 A-to-I Human chr1 + 52085694 52085694 52085694 CAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCTGGGTATGGTGGTGTTTGCCT CAACATGGTGAAACCCCATCTCTACTAAAAATTCAAAAATTAGCTGGGTATGGTGGTGTTTGCCT A T BTF3L4 Ensembl:ENSG00000134717 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1029547537 Functional Loss SNV dbSNP153 33..33 33 - - - 43039 RMVar_ID_43039 Human_SNP_ID_13343882 A-to-I Human chr1 - 52160415 52160415 52160415 ATAGAAAGGCACTGCCTTTGGAGGATGGAAGAATGTAGAAAGTGTCCCAAAGTTGGTGTCTGAAT ATAGAAAGGCACTGCCTTTGGAGGATGGAAGATTGTAGAAAGTGTCCCAAAGTTGGTGTCTGAAT T A AL139156.2 Ensembl:ENSG00000228407 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs895743072 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5890997 43040 RMVar_ID_43040 Human_SNP_ID_13367646 A-to-I Human chr1 + 52255464 52255464 52255464 AAAATTAGCCGGGCATGGTGGCACATGCCTGTAGTCCCGGCTACTCAGGGGGCTGAGGCAGGAGA AAAATTAGCCGGGCATGGTGGCACATGCCTGTGGTCCCGGCTACTCAGGGGGCTGAGGCAGGAGA A G ZFYVE9 Ensembl:ENSG00000157077 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1224837170 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14955,RMVar_hsa_circ_25766,RMVar_hsa_circ_88177,RMVar_hsa_circ_366964,RMVar_hsa_circ_106020,RMVar_hsa_circ_73091,RMVar_hsa_circ_132926,RMVar_hsa_circ_132927,RMVar_hsa_circ_73707,RMVar_hsa_circ_124205,RMVar_hsa_circ_52716,RMVar_hsa_circ_132928 43041 RMVar_ID_43041 Human_SNP_ID_13391369 A-to-I Human chr1 + 52349983 52349983 52349983 TCTTGTTGCCCAGACTGGAGTGCAATGGCACTATCTCGGCTCACTGCAACCACCGCCTCCCGGGT TCTTGTTGCCCAGACTGGAGTGCAATGGCACTGTCTCGGCTCACTGCAACCACCGCCTCCCGGGT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1328051076 Functional Loss SNV dbSNP153 33..33 33 - - - 43042 RMVar_ID_43042 Human_SNP_ID_13391601 A-to-I Human chr1 - 52350919 52350919 52350919 AACATGGTGAAACCCCGTCTCCACTAAAAACAAAAACAATTAGCTGGGCATGGTGGCCGGCGCCT AACATGGTGAAACCCCGTCTCCACTAAAAACAGAAACAATTAGCTGGGCATGGTGGCCGGCGCCT T C CC2D1B Ensembl:ENSG00000154222 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1051336817 Functional Loss SNV dbSNP153 33..33 33 - - - 43043 RMVar_ID_43043 Human_SNP_ID_13391610 A-to-I Human chr1 - 52350965 52350965 52350965 AGGCAGGTGGATCACCTGAGGTCAGGAATTCAAGACCAGCCTGGCCAACATGGTGAAACCCCGTC AGGCAGGTGGATCACCTGAGGTCAGGAATTCAGGACCAGCCTGGCCAACATGGTGAAACCCCGTC T C CC2D1B Ensembl:ENSG00000154222 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs893188346 Functional Loss SNV dbSNP153 33..33 33 - - - 43044 RMVar_ID_43044 Human_SNP_ID_13391787 A-to-I Human chr1 - 52351642 52351642 52351642 TGACCTCATGATCCACCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCAC TGACCTCATGATCCACCCACCTCAGCCTCCCACAGTGCTGGGATTACAGGTGTGAGCCACCGCAC T G CC2D1B Ensembl:ENSG00000154222 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs980063269 Functional Loss SNV dbSNP153 33..33 33 - - - 43045 RMVar_ID_43045 Human_SNP_ID_13391816 A-to-I Human chr1 - 52351721 52351721 52351721 CACCACTATGCCCAGCTAATTTTTTTATTTTTAGTAGAGACGGTGTTTCACCATGTTGGTCAGGC CACCACTATGCCCAGCTAATTTTTTTATTTTTGGTAGAGACGGTGTTTCACCATGTTGGTCAGGC T C CC2D1B Ensembl:ENSG00000154222 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1228053251 Functional Loss SNV dbSNP153 33..33 33 - - - 43046 RMVar_ID_43046 Human_SNP_ID_13391844 A-to-I Human chr1 - 52351815 52351815 52351815 CAGTGGCATGATCTCAGCTCGCTGCAACCCCCACCTCCCAGGTTCAAGCGATTCTCCTGTGTCAG CAGTGGCATGATCTCAGCTCGCTGCAACCCCCGCCTCCCAGGTTCAAGCGATTCTCCTGTGTCAG T C CC2D1B Ensembl:ENSG00000154222 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1371733933 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1416789,Human_miRNA_ID_1700505 43047 RMVar_ID_43047 Human_SNP_ID_13391867 A-to-I Human chr1 - 52351878 52351878 52351878 GCCGATTTTTTTTTTTTTTTTTTTTTTGAGACAGAGTAGCTCTCTGCCAGCCAGGCTGGAGTGCA GCCGATTTTTTTTTTTTTTTTTTTTTTGAGACGGAGTAGCTCTCTGCCAGCCAGGCTGGAGTGCA T C CC2D1B Ensembl:ENSG00000154222 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1285371052 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2154041 43048 RMVar_ID_43048 Human_SNP_ID_13398318 A-to-I Human chr1 - 52373024 52373024 52373024 AGGCTTAGGTGACCCCCCAACCTCATCCTCCCAGGTGGCTGAAACTACAGGCACATGCCACCATG AGGCTTAGGTGACCCCCCAACCTCATCCTCCCTGGTGGCTGAAACTACAGGCACATGCCACCATG T A ORC1 Ensembl:ENSG00000085840 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232137109 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_357688,Human_RBP_ID_5457813,Human_RBP_ID_24398632,Human_RBP_ID_26798422 RMVar_hsa_circ_132953,RMVar_hsa_circ_99812,RMVar_hsa_circ_109883,RMVar_hsa_circ_116916,RMVar_hsa_circ_105694,RMVar_hsa_circ_107236,RMVar_hsa_circ_104536,RMVar_hsa_circ_132955,RMVar_hsa_circ_132957,RMVar_hsa_circ_89324,RMVar_hsa_circ_132958,RMVar_hsa_circ_132956,RMVar_hsa_circ_132954,RMVar_hsa_circ_132952 43049 RMVar_ID_43049 Human_SNP_ID_13401804 A-to-I Human chr1 - 52386785 52386785 52386785 CATCATGCCTAGCTAATTTAGAGGGGGCTTTCACCTCTGTGTTGCCCAGGCTGTCCTCAAACTCC CATCATGCCTAGCTAATTTAGAGGGGGCTTTCGCCTCTGTGTTGCCCAGGCTGTCCTCAAACTCC T C ORC1 Ensembl:ENSG00000085840 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs761768949 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_132953,RMVar_hsa_circ_99812,RMVar_hsa_circ_105694,RMVar_hsa_circ_89324,RMVar_hsa_circ_132954,RMVar_hsa_circ_80590,RMVar_hsa_circ_132952,RMVar_hsa_circ_340390,RMVar_hsa_circ_76183,RMVar_hsa_circ_132959,RMVar_hsa_circ_16873,RMVar_hsa_circ_330155,RMVar_hsa_circ_109647,RMVar_hsa_circ_132961,RMVar_hsa_circ_132962 43050 RMVar_ID_43050 Human_SNP_ID_13401831 A-to-I Human chr1 - 52386889 52386889 52386889 TGGAGTGCAGTGGTGCAATCTCAACTCACTGTAGCCTCAACCTCCTGGGCTCAAGCGATCCTTCC TGGAGTGCAGTGGTGCAATCTCAACTCACTGTCGCCTCAACCTCCTGGGCTCAAGCGATCCTTCC T G ORC1 Ensembl:ENSG00000085840 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1246476820 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_132953,RMVar_hsa_circ_99812,RMVar_hsa_circ_105694,RMVar_hsa_circ_89324,RMVar_hsa_circ_132954,RMVar_hsa_circ_80590,RMVar_hsa_circ_132952,RMVar_hsa_circ_340390,RMVar_hsa_circ_76183,RMVar_hsa_circ_132959,RMVar_hsa_circ_16873,RMVar_hsa_circ_330155,RMVar_hsa_circ_109647,RMVar_hsa_circ_132961,RMVar_hsa_circ_132962 43051 RMVar_ID_43051 Human_SNP_ID_13401834 A-to-I Human chr1 - 52386904 52386904 52386904 GTCTCTTGCCCAGGCTGGAGTGCAGTGGTGCAATCTCAACTCACTGTAGCCTCAACCTCCTGGGC GTCTCTTGCCCAGGCTGGAGTGCAGTGGTGCAGTCTCAACTCACTGTAGCCTCAACCTCCTGGGC T C ORC1 Ensembl:ENSG00000085840 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1034308048 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_132953,RMVar_hsa_circ_99812,RMVar_hsa_circ_105694,RMVar_hsa_circ_89324,RMVar_hsa_circ_132954,RMVar_hsa_circ_80590,RMVar_hsa_circ_132952,RMVar_hsa_circ_340390,RMVar_hsa_circ_76183,RMVar_hsa_circ_132959,RMVar_hsa_circ_16873,RMVar_hsa_circ_330155,RMVar_hsa_circ_109647,RMVar_hsa_circ_132961,RMVar_hsa_circ_132962 43052 RMVar_ID_43052 Human_SNP_ID_13401835 A-to-I Human chr1 - 52386905 52386905 52386905 TGTCTCTTGCCCAGGCTGGAGTGCAGTGGTGCAATCTCAACTCACTGTAGCCTCAACCTCCTGGG TGTCTCTTGCCCAGGCTGGAGTGCAGTGGTGCGATCTCAACTCACTGTAGCCTCAACCTCCTGGG T C ORC1 Ensembl:ENSG00000085840 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs968110270 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_132953,RMVar_hsa_circ_99812,RMVar_hsa_circ_105694,RMVar_hsa_circ_89324,RMVar_hsa_circ_132954,RMVar_hsa_circ_80590,RMVar_hsa_circ_132952,RMVar_hsa_circ_340390,RMVar_hsa_circ_76183,RMVar_hsa_circ_132959,RMVar_hsa_circ_16873,RMVar_hsa_circ_330155,RMVar_hsa_circ_109647,RMVar_hsa_circ_132961,RMVar_hsa_circ_132962 43053 RMVar_ID_43053 Human_SNP_ID_13402006 A-to-I Human chr1 - 52387652 52387652 52387652 GAATTCAAGACCAGCCTGGCCAACAATGGTGAAACCCTGTCTCTGCTTAAAATACAAAAATTAGC GAATTCAAGACCAGCCTGGCCAACAATGGTGATACCCTGTCTCTGCTTAAAATACAAAAATTAGC T A ORC1 Ensembl:ENSG00000085840 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1309426332 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_132953,RMVar_hsa_circ_99812,RMVar_hsa_circ_105694,RMVar_hsa_circ_89324,RMVar_hsa_circ_132954,RMVar_hsa_circ_80590,RMVar_hsa_circ_132952,RMVar_hsa_circ_340390,RMVar_hsa_circ_76183,RMVar_hsa_circ_132959,RMVar_hsa_circ_16873,RMVar_hsa_circ_330155,RMVar_hsa_circ_109647,RMVar_hsa_circ_132961,RMVar_hsa_circ_132962 43054 RMVar_ID_43054 Human_SNP_ID_13407862 A-to-I Human chr1 + 52410601 52410601 52410601 TCAGGTCACTGCAACCTCTGCCTCCCAGGTTCAAATAATTCTCCTGCCTCAGCCTCTTGAGTAGC TCAGGTCACTGCAACCTCTGCCTCCCAGGTTCCAATAATTCTCCTGCCTCAGCCTCTTGAGTAGC A C PRPF38A Ensembl:ENSG00000134748 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017071100 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_185,RMVar_hsa_circ_51920 43055 RMVar_ID_43055 Human_SNP_ID_13407930 A-to-I Human chr1 + 52410890 52410890 52410890 AACATTGAAGGTTCAGATGAGAAATTATATTTAAGTTATATGATCTCTTCAAGATCATCCCTACA AACATTGAAGGTTCAGATGAGAAATTATATTTGAGTTATATGATCTCTTCAAGATCATCCCTACA A G PRPF38A Ensembl:ENSG00000134748 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11205954 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_185,RMVar_hsa_circ_51920 43056 RMVar_ID_43056 Human_SNP_ID_13408569 A-to-I Human chr1 + 52413581 52413581 52413581 GCATACCTGGCTAATTTGTGTATTTTTTTTGTAGAGATGGGATTTCACCATGTTGCCCAGGCTGC GCATACCTGGCTAATTTGTGTATTTTTTTTGTGGAGATGGGATTTCACCATGTTGCCCAGGCTGC A G PRPF38A Ensembl:ENSG00000134748 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1304133496 Functional Loss SNV dbSNP153 33..33 33 - - - 43057 RMVar_ID_43057 Human_SNP_ID_13412754 A-to-I Human chr1 - 52429488 52429488 52429488 CAGTGGCTATTCACAGGCCAATCTAGCATACTACAACCTTGAACTCCTGGGCTCAAGTGCTCCTC CAGTGGCTATTCACAGGCCAATCTAGCATACTGCAACCTTGAACTCCTGGGCTCAAGTGCTCCTC T C TUT4 Ensembl:ENSG00000134744 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1462752632 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8314280 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_132969 43058 RMVar_ID_43058 Human_SNP_ID_13413633 A-to-I Human chr1 - 52433244 52433244 52433244 CAACATGGTAAAACCCCATCTCTGCTAAAACTACAAAAAATTAGCTGGATGTGGTGGCAGGGAAC CAACATGGTAAAACCCCATCTCTGCTAAAACTGCAAAAAATTAGCTGGATGTGGTGGCAGGGAAC T C TUT4 Ensembl:ENSG00000134744 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017551061 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24767078 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 43059 RMVar_ID_43059 Human_SNP_ID_13415263 A-to-I Human chr1 - 52440330 52440330 52440330 GGCCAGGAGTTCAAGACCAGCCTGGCCAACACAGCGAGATGCTGTCTCTAAAAAACCAAATAAAA GGCCAGGAGTTCAAGACCAGCCTGGCCAACACTGCGAGATGCTGTCTCTAAAAAACCAAATAAAA T A TUT4 Ensembl:ENSG00000134744 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1450029087 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88452,RMVar_hsa_circ_84080,RMVar_hsa_circ_132970,RMVar_hsa_circ_132974,RMVar_hsa_circ_132969,RMVar_hsa_circ_301483,RMVar_hsa_circ_319783,RMVar_hsa_circ_132978,RMVar_hsa_circ_285884,RMVar_hsa_circ_132976,RMVar_hsa_circ_132975,RMVar_hsa_circ_288835,RMVar_hsa_circ_355709,RMVar_hsa_circ_369758,RMVar_hsa_circ_354475,RMVar_hsa_circ_51994,RMVar_hsa_circ_103317,RMVar_hsa_circ_132979,RMVar_hsa_circ_132977 43060 RMVar_ID_43060 Human_SNP_ID_13415277 A-to-I Human chr1 - 52440387 52440387 52440387 GGTGGCTCATGCCTGTAATCTATTACTTTGGAAGGCCAGGGCAGGAAGATCGCTTGAGGCCAGGA GGTGGCTCATGCCTGTAATCTATTACTTTGGACGGCCAGGGCAGGAAGATCGCTTGAGGCCAGGA T G TUT4 Ensembl:ENSG00000134744 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1463293346 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88452,RMVar_hsa_circ_84080,RMVar_hsa_circ_132970,RMVar_hsa_circ_132974,RMVar_hsa_circ_132969,RMVar_hsa_circ_301483,RMVar_hsa_circ_319783,RMVar_hsa_circ_132978,RMVar_hsa_circ_285884,RMVar_hsa_circ_132976,RMVar_hsa_circ_132975,RMVar_hsa_circ_288835,RMVar_hsa_circ_355709,RMVar_hsa_circ_369758,RMVar_hsa_circ_354475,RMVar_hsa_circ_51994,RMVar_hsa_circ_103317,RMVar_hsa_circ_132979,RMVar_hsa_circ_132977 43061 RMVar_ID_43061 Human_SNP_ID_13415496 A-to-I Human chr1 - 52441344 52441344 52441344 GGGAGGCGGAGGTTGCATTGAGCTGAGATTGCAGCACTGCACTCCAGCCTGGGCAACAGAACGAC GGGAGGCGGAGGTTGCATTGAGCTGAGATTGCGGCACTGCACTCCAGCCTGGGCAACAGAACGAC T C TUT4 Ensembl:ENSG00000134744 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054954207 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24767108 RMVar_hsa_circ_88452,RMVar_hsa_circ_84080,RMVar_hsa_circ_132970,RMVar_hsa_circ_132974,RMVar_hsa_circ_132969,RMVar_hsa_circ_301483,RMVar_hsa_circ_319783,RMVar_hsa_circ_132978,RMVar_hsa_circ_285884,RMVar_hsa_circ_132976,RMVar_hsa_circ_132975,RMVar_hsa_circ_288835,RMVar_hsa_circ_355709,RMVar_hsa_circ_369758,RMVar_hsa_circ_354475,RMVar_hsa_circ_51994,RMVar_hsa_circ_103317,RMVar_hsa_circ_132979,RMVar_hsa_circ_132977 43062 RMVar_ID_43062 Human_SNP_ID_13415674 A-to-I Human chr1 - 52441996 52441994 52441996 GCCCAGATAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCACGCTGGCCAGGCTGGTCACAA GCCCAGATAATTTTTGTATTTTTAGTAGAGAC__GGTTTCACCACGCTGGCCAGGCTGGTCACAA CCT C TUT4 Ensembl:ENSG00000134744 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1195483844 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_88452,RMVar_hsa_circ_84080,RMVar_hsa_circ_132970,RMVar_hsa_circ_132974,RMVar_hsa_circ_132969,RMVar_hsa_circ_301483,RMVar_hsa_circ_319783,RMVar_hsa_circ_132978,RMVar_hsa_circ_285884,RMVar_hsa_circ_132976,RMVar_hsa_circ_132975,RMVar_hsa_circ_288835,RMVar_hsa_circ_355709,RMVar_hsa_circ_369758,RMVar_hsa_circ_354475,RMVar_hsa_circ_51994,RMVar_hsa_circ_103317,RMVar_hsa_circ_132979,RMVar_hsa_circ_132977 43063 RMVar_ID_43063 Human_SNP_ID_13416228 A-to-I Human chr1 - 52444092 52444092 52444092 AGCAGGGACCACAGGCGCCCGACACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGAGGGGAT AGCAGGGACCACAGGCGCCCGACACCACGCCCGGCTAATTTTTGTATTTTTAGTAGAGAGGGGAT T C TUT4 Ensembl:ENSG00000134744 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910285280 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88452,RMVar_hsa_circ_84080,RMVar_hsa_circ_132970,RMVar_hsa_circ_132974,RMVar_hsa_circ_132969,RMVar_hsa_circ_301483,RMVar_hsa_circ_319783,RMVar_hsa_circ_132978,RMVar_hsa_circ_285884,RMVar_hsa_circ_132976,RMVar_hsa_circ_132975,RMVar_hsa_circ_288835,RMVar_hsa_circ_355709,RMVar_hsa_circ_369758,RMVar_hsa_circ_354475,RMVar_hsa_circ_51994,RMVar_hsa_circ_103317,RMVar_hsa_circ_132979,RMVar_hsa_circ_132977 43064 RMVar_ID_43064 Human_SNP_ID_13421868 A-to-I Human chr1 - 52466450 52466450 52466450 TTTGTAGAGATGGAGTCTCACCATGTTTTCCAAGCAGGTCTCAAACTCCTGAACTCAAGTGATCC TTTGTAGAGATGGAGTCTCACCATGTTTTCCAGGCAGGTCTCAAACTCCTGAACTCAAGTGATCC T C TUT4 Ensembl:ENSG00000134744 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1369665049 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6600,RMVar_hsa_circ_88452,RMVar_hsa_circ_84080,RMVar_hsa_circ_132970,RMVar_hsa_circ_132969,RMVar_hsa_circ_132980,RMVar_hsa_circ_287826,RMVar_hsa_circ_355709,RMVar_hsa_circ_51994,RMVar_hsa_circ_318934,RMVar_hsa_circ_368365,RMVar_hsa_circ_324579,RMVar_hsa_circ_48770,RMVar_hsa_circ_132981,RMVar_hsa_circ_132990,RMVar_hsa_circ_320451,RMVar_hsa_circ_333343,RMVar_hsa_circ_324314,RMVar_hsa_circ_292321,RMVar_hsa_circ_279161,RMVar_hsa_circ_132988,RMVar_hsa_circ_132989,RMVar_hsa_circ_132987,RMVar_hsa_circ_338684,RMVar_hsa_circ_365322,RMVar_hsa_circ_47367,RMVar_hsa_circ_132996,RMVar_hsa_circ_109577,RMVar_hsa_circ_91144,RMVar_hsa_circ_121402,RMVar_hsa_circ_36633,RMVar_hsa_circ_132991,RMVar_hsa_circ_132992,RMVar_hsa_circ_126304,RMVar_hsa_circ_314343,RMVar_hsa_circ_132993,RMVar_hsa_circ_132994,RMVar_hsa_circ_357107,RMVar_hsa_circ_132995,RMVar_hsa_circ_367602,RMVar_hsa_circ_337908,RMVar_hsa_circ_300334,RMVar_hsa_circ_302742,RMVar_hsa_circ_132997 43065 RMVar_ID_43065 Human_SNP_ID_13429617 A-to-I Human chr1 - 52498824 52498824 52498824 GGAGTGCAGTGGTGCGATCTTGACTCACTGCAAGCTCCACCTCCGAGGTTGAAACGATTCTCCTG GGAGTGCAGTGGTGCGATCTTGACTCACTGCAGGCTCCACCTCCGAGGTTGAAACGATTCTCCTG T C TUT4 Ensembl:ENSG00000134744 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1307473920 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56837,RMVar_hsa_circ_88452,RMVar_hsa_circ_132969,RMVar_hsa_circ_368365,RMVar_hsa_circ_132990,RMVar_hsa_circ_333343,RMVar_hsa_circ_132996,RMVar_hsa_circ_91144,RMVar_hsa_circ_121402,RMVar_hsa_circ_132991,RMVar_hsa_circ_132992,RMVar_hsa_circ_126304,RMVar_hsa_circ_132994,RMVar_hsa_circ_302742,RMVar_hsa_circ_299170,RMVar_hsa_circ_67601,RMVar_hsa_circ_61539,RMVar_hsa_circ_133003,RMVar_hsa_circ_378205,RMVar_hsa_circ_70930,RMVar_hsa_circ_32729,RMVar_hsa_circ_349466,RMVar_hsa_circ_4981,RMVar_hsa_circ_113320,RMVar_hsa_circ_63614,RMVar_hsa_circ_133012,RMVar_hsa_circ_290560,RMVar_hsa_circ_317013,RMVar_hsa_circ_133014,RMVar_hsa_circ_324946,RMVar_hsa_circ_368345,RMVar_hsa_circ_275302,RMVar_hsa_circ_133020,RMVar_hsa_circ_133021,RMVar_hsa_circ_133019,RMVar_hsa_circ_281040,RMVar_hsa_circ_133022,RMVar_hsa_circ_329383,RMVar_hsa_circ_279879,RMVar_hsa_circ_133025,RMVar_hsa_circ_133026,RMVar_hsa_circ_65331,RMVar_hsa_circ_293334,RMVar_hsa_circ_107563,RMVar_hsa_circ_133027,RMVar_hsa_circ_133028 43066 RMVar_ID_43066 Human_SNP_ID_13429787 A-to-I Human chr1 - 52499236 52499236 52499236 TGCCACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGGTGGGGTTTCTCCATGTTGGCCTGTC TGCCACCATGCCTGGCTAATTTTTGTATTTTTGGTAGAGGTGGGGTTTCTCCATGTTGGCCTGTC T C TUT4 Ensembl:ENSG00000134744 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs887568850 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11030038 RMVar_hsa_circ_56837,RMVar_hsa_circ_88452,RMVar_hsa_circ_132969,RMVar_hsa_circ_368365,RMVar_hsa_circ_132990,RMVar_hsa_circ_333343,RMVar_hsa_circ_132996,RMVar_hsa_circ_91144,RMVar_hsa_circ_121402,RMVar_hsa_circ_132991,RMVar_hsa_circ_132992,RMVar_hsa_circ_126304,RMVar_hsa_circ_132994,RMVar_hsa_circ_302742,RMVar_hsa_circ_299170,RMVar_hsa_circ_67601,RMVar_hsa_circ_61539,RMVar_hsa_circ_133003,RMVar_hsa_circ_378205,RMVar_hsa_circ_70930,RMVar_hsa_circ_32729,RMVar_hsa_circ_349466,RMVar_hsa_circ_4981,RMVar_hsa_circ_113320,RMVar_hsa_circ_63614,RMVar_hsa_circ_133012,RMVar_hsa_circ_290560,RMVar_hsa_circ_317013,RMVar_hsa_circ_133014,RMVar_hsa_circ_324946,RMVar_hsa_circ_368345,RMVar_hsa_circ_275302,RMVar_hsa_circ_133020,RMVar_hsa_circ_133021,RMVar_hsa_circ_133019,RMVar_hsa_circ_281040,RMVar_hsa_circ_133022,RMVar_hsa_circ_329383,RMVar_hsa_circ_279879,RMVar_hsa_circ_133025,RMVar_hsa_circ_133026,RMVar_hsa_circ_65331,RMVar_hsa_circ_293334,RMVar_hsa_circ_107563,RMVar_hsa_circ_133027,RMVar_hsa_circ_133028 43067 RMVar_ID_43067 Human_SNP_ID_13431066 A-to-I Human chr1 - 52504611 52504611 52504611 GTTTGTTTTTTTTCAAGATAGAGTCTTGCTCTATCGCCCAGACTGAAGTGCAGTGGCGCTATCTC GTTTGTTTTTTTTCAAGATAGAGTCTTGCTCTGTCGCCCAGACTGAAGTGCAGTGGCGCTATCTC T C TUT4 Ensembl:ENSG00000134744 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879565967 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56837,RMVar_hsa_circ_88452,RMVar_hsa_circ_132969,RMVar_hsa_circ_368365,RMVar_hsa_circ_132990,RMVar_hsa_circ_333343,RMVar_hsa_circ_132996,RMVar_hsa_circ_91144,RMVar_hsa_circ_121402,RMVar_hsa_circ_132991,RMVar_hsa_circ_132992,RMVar_hsa_circ_126304,RMVar_hsa_circ_132994,RMVar_hsa_circ_302742,RMVar_hsa_circ_299170,RMVar_hsa_circ_67601,RMVar_hsa_circ_61539,RMVar_hsa_circ_133003,RMVar_hsa_circ_378205,RMVar_hsa_circ_70930,RMVar_hsa_circ_32729,RMVar_hsa_circ_349466,RMVar_hsa_circ_4981,RMVar_hsa_circ_113320,RMVar_hsa_circ_63614,RMVar_hsa_circ_133012,RMVar_hsa_circ_290560,RMVar_hsa_circ_317013,RMVar_hsa_circ_133014,RMVar_hsa_circ_324946,RMVar_hsa_circ_368345,RMVar_hsa_circ_275302,RMVar_hsa_circ_133020,RMVar_hsa_circ_133021,RMVar_hsa_circ_133019,RMVar_hsa_circ_281040,RMVar_hsa_circ_133022,RMVar_hsa_circ_329383,RMVar_hsa_circ_279879,RMVar_hsa_circ_133025,RMVar_hsa_circ_133026,RMVar_hsa_circ_65331,RMVar_hsa_circ_293334,RMVar_hsa_circ_107563,RMVar_hsa_circ_133027,RMVar_hsa_circ_133028 43068 RMVar_ID_43068 Human_SNP_ID_13433391 A-to-I Human chr1 - 52514256 52514256 52514256 TTGTATTTTTAGTAGAGACGGGGTTTCACTATATTGGCCAGTTTGGTCTCGAACTCCTGACCTCA TTGTATTTTTAGTAGAGACGGGGTTTCACTATGTTGGCCAGTTTGGTCTCGAACTCCTGACCTCA T C TUT4 Ensembl:ENSG00000134744 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs780916965 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56837,RMVar_hsa_circ_88452,RMVar_hsa_circ_132969,RMVar_hsa_circ_121402,RMVar_hsa_circ_132992,RMVar_hsa_circ_67601,RMVar_hsa_circ_61539,RMVar_hsa_circ_378205,RMVar_hsa_circ_32729,RMVar_hsa_circ_4981,RMVar_hsa_circ_113320,RMVar_hsa_circ_63614,RMVar_hsa_circ_324946,RMVar_hsa_circ_368345,RMVar_hsa_circ_133020,RMVar_hsa_circ_133021,RMVar_hsa_circ_329383,RMVar_hsa_circ_17200,RMVar_hsa_circ_133026,RMVar_hsa_circ_65331,RMVar_hsa_circ_270080,RMVar_hsa_circ_358627,RMVar_hsa_circ_133030,RMVar_hsa_circ_133032,RMVar_hsa_circ_133033,RMVar_hsa_circ_133034,RMVar_hsa_circ_133031 43069 RMVar_ID_43069 Human_SNP_ID_13433418 A-to-I Human chr1 - 52514354 52514354 52514354 TCACTGCAACCTCTACCTCCTGGGTTCAAGCAATTCTCCTGCCTCAGCCTCTTAAGTAGCTGGTA TCACTGCAACCTCTACCTCCTGGGTTCAAGCAGTTCTCCTGCCTCAGCCTCTTAAGTAGCTGGTA T C TUT4 Ensembl:ENSG00000134744 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1002869300 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56837,RMVar_hsa_circ_88452,RMVar_hsa_circ_132969,RMVar_hsa_circ_121402,RMVar_hsa_circ_132992,RMVar_hsa_circ_67601,RMVar_hsa_circ_61539,RMVar_hsa_circ_378205,RMVar_hsa_circ_32729,RMVar_hsa_circ_4981,RMVar_hsa_circ_113320,RMVar_hsa_circ_63614,RMVar_hsa_circ_324946,RMVar_hsa_circ_368345,RMVar_hsa_circ_133020,RMVar_hsa_circ_133021,RMVar_hsa_circ_329383,RMVar_hsa_circ_17200,RMVar_hsa_circ_133026,RMVar_hsa_circ_65331,RMVar_hsa_circ_270080,RMVar_hsa_circ_358627,RMVar_hsa_circ_133030,RMVar_hsa_circ_133032,RMVar_hsa_circ_133033,RMVar_hsa_circ_133034,RMVar_hsa_circ_133031 43070 RMVar_ID_43070 Human_SNP_ID_13433574 A-to-I Human chr1 - 52514942 52514942 52514942 GAAACCCCGTCTCTACTAAAAATACAAAAATTAGCGAGGTGTGGTAGTCGGTACCTGTAGTCCCA GAAACCCCGTCTCTACTAAAAATACAAAAATTGGCGAGGTGTGGTAGTCGGTACCTGTAGTCCCA T C TUT4 Ensembl:ENSG00000134744 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886462443 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11030445 RMVar_hsa_circ_56837,RMVar_hsa_circ_88452,RMVar_hsa_circ_132969,RMVar_hsa_circ_121402,RMVar_hsa_circ_132992,RMVar_hsa_circ_67601,RMVar_hsa_circ_61539,RMVar_hsa_circ_378205,RMVar_hsa_circ_32729,RMVar_hsa_circ_4981,RMVar_hsa_circ_113320,RMVar_hsa_circ_63614,RMVar_hsa_circ_324946,RMVar_hsa_circ_368345,RMVar_hsa_circ_133020,RMVar_hsa_circ_133021,RMVar_hsa_circ_329383,RMVar_hsa_circ_17200,RMVar_hsa_circ_133026,RMVar_hsa_circ_65331,RMVar_hsa_circ_270080,RMVar_hsa_circ_358627,RMVar_hsa_circ_133030,RMVar_hsa_circ_133032,RMVar_hsa_circ_133033,RMVar_hsa_circ_133034,RMVar_hsa_circ_133031 43071 RMVar_ID_43071 Human_SNP_ID_13435594 A-to-I Human chr1 - 52523457 52523457 52523457 GGGACTACAGGTGTGCGCCACCATGCCTGGCTAATTCTATATTTTTAGTAGAGACTGGGTTTCAC GGGACTACAGGTGTGCGCCACCATGCCTGGCTGATTCTATATTTTTAGTAGAGACTGGGTTTCAC T C TUT4 Ensembl:ENSG00000134744 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs984026738 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56837,RMVar_hsa_circ_88452,RMVar_hsa_circ_132969,RMVar_hsa_circ_121402,RMVar_hsa_circ_132992,RMVar_hsa_circ_67601,RMVar_hsa_circ_378205,RMVar_hsa_circ_4981,RMVar_hsa_circ_113320,RMVar_hsa_circ_324946,RMVar_hsa_circ_133020,RMVar_hsa_circ_133021,RMVar_hsa_circ_329383,RMVar_hsa_circ_17200,RMVar_hsa_circ_133026,RMVar_hsa_circ_65331,RMVar_hsa_circ_270080,RMVar_hsa_circ_133032,RMVar_hsa_circ_133033,RMVar_hsa_circ_133034,RMVar_hsa_circ_133031,RMVar_hsa_circ_133035,RMVar_hsa_circ_271904 43072 RMVar_ID_43072 Human_SNP_ID_13438324 A-to-I Human chr1 - 52533776 52533776 52533776 GTATTTTAATAGAGACGAGATTTCGCCATGCCAGGCCAGTCTTGAACTCCTGGCCTCAAGTGATC GTATTTTAATAGAGACGAGATTTCGCCATGCCGGGCCAGTCTTGAACTCCTGGCCTCAAGTGATC T C TUT4 Ensembl:ENSG00000134744 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1428927284 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121402,RMVar_hsa_circ_132992,RMVar_hsa_circ_4981,RMVar_hsa_circ_113320,RMVar_hsa_circ_133021,RMVar_hsa_circ_17200,RMVar_hsa_circ_133034 43073 RMVar_ID_43073 Human_SNP_ID_13473927 A-to-I Human chr1 - 52685765 52685765 52685765 GGTCAGGATTTCGAGAACAGCCTGGCCAACATAGTGAAACCTCGTATCTACTAAAAATACAAAAA GGTCAGGATTTCGAGAACAGCCTGGCCAACATGGTGAAACCTCGTATCTACTAAAAATACAAAAA T C COA7 Ensembl:ENSG00000162377 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1354541450 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8240909,Human_RBP_ID_11031343 43074 RMVar_ID_43074 Human_SNP_ID_13476716 A-to-I Human chr1 - 52697107 52697107 52697107 ACTGCCTACTTTTTAATTTTTTTGTTTTTTTGAGACTGAGTCTCACTCTGTCACCCAGGCTGGAG ACTGCCTACTTTTTAATTTTTTTGTTTTTTTGGGACTGAGTCTCACTCTGTCACCCAGGCTGGAG T C COA7 Ensembl:ENSG00000162377 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1336965643 Functional Loss SNV dbSNP153 33..33 33 - - - 43075 RMVar_ID_43075 Human_SNP_ID_13496159 A-to-I Human chr1 - 52772288 52772288 52772288 TGCTAAATTCCATCTGATTCTGATAGAGAGCCAGATTCACCGTTTGGCTCAATATTATAAGACCA TGCTAAATTCCATCTGATTCTGATAGAGAGCCGGATTCACCGTTTGGCTCAATATTATAAGACCA T C RPS13P2 Ensembl:ENSG00000228929 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs547897384 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1829579 43076 RMVar_ID_43076 Human_SNP_ID_13496163 A-to-I Human chr1 - 52772309 52772309 52772309 GAGGAACAGAAAGGATAAGGATGCTAAATTCCATCTGATTCTGATAGAGAGCCAGATTCACCGTT GAGGAACAGAAAGGATAAGGATGCTAAATTCCGTCTGATTCTGATAGAGAGCCAGATTCACCGTT T C RPS13P2 Ensembl:ENSG00000228929 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879110331 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1432683,Human_RBP_ID_1750474,Human_RBP_ID_5890045,Human_RBP_ID_8314412,Human_RBP_ID_17678190,Human_RBP_ID_18577655,Human_RBP_ID_26381340 Human_miRNA_ID_1840379,Human_miRNA_ID_1861689 43077 RMVar_ID_43077 Human_SNP_ID_13496672 A-to-I Human chr1 + 52773857 52773857 52773857 TAGAGACAGGGGTTCACCATGTTGCCAAGGCTAGTCTCGAACTCCTGAGCTCAGGCAGTTCGCCT TAGAGACAGGGGTTCACCATGTTGCCAAGGCTGGTCTCGAACTCCTGAGCTCAGGCAGTTCGCCT A G ZYG11B Ensembl:ENSG00000162378 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968678808 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97549,RMVar_hsa_circ_315561,RMVar_hsa_circ_58114,RMVar_hsa_circ_324243,RMVar_hsa_circ_23803,RMVar_hsa_circ_42684,RMVar_hsa_circ_352964,RMVar_hsa_circ_341889,RMVar_hsa_circ_320181,RMVar_hsa_circ_309774,RMVar_hsa_circ_133043,RMVar_hsa_circ_133044,RMVar_hsa_circ_133045,RMVar_hsa_circ_133042 43078 RMVar_ID_43078 Human_SNP_ID_13505661 A-to-I Human chr1 + 52803735 52803735 52803735 GCAATCTTCTCACCTTAGCCTCCAGAGTAGCTAGGACTATAGGCATGTGCCACCATGCCCAGCTT GCAATCTTCTCACCTTAGCCTCCAGAGTAGCTGGGACTATAGGCATGTGCCACCATGCCCAGCTT A G ZYG11B Ensembl:ENSG00000162378 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs779276687 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97549,RMVar_hsa_circ_58114,RMVar_hsa_circ_133045,RMVar_hsa_circ_90122,RMVar_hsa_circ_127307,RMVar_hsa_circ_133051,RMVar_hsa_circ_133053,RMVar_hsa_circ_335435 43079 RMVar_ID_43079 Human_SNP_ID_13509009 A-to-I Human chr1 + 52817583 52817583 52817583 TTTTTTTGTATTTTTTGTAGAGATGGGGTTTCATCATGTTGGCCAGGCTGGTGTCAAACTCCTAG TTTTTTTGTATTTTTTGTAGAGATGGGGTTTCGTCATGTTGGCCAGGCTGGTGTCAAACTCCTAG A G ZYG11B Ensembl:ENSG00000162378 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs915717412 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 43080 RMVar_ID_43080 Human_SNP_ID_13509481 A-to-I Human chr1 + 52818863 52818863 52818863 TTGCCCAGGCTGGAGTGCAGTGACACGATCTCAGCTCACCACAACCTACACCTCCCAGATTCAAG TTGCCCAGGCTGGAGTGCAGTGACACGATCTCCGCTCACCACAACCTACACCTCCCAGATTCAAG A C ZYG11B Ensembl:ENSG00000162378 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs933161845 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 43081 RMVar_ID_43081 Human_SNP_ID_13509706 A-to-I Human chr1 + 52819679 52819679 52819679 GGTTGTGGCACACATCTGTACTCTCAGCTACTAGGGAGGCTGAGGCAGGAAAATCACTTGAACTG GGTTGTGGCACACATCTGTACTCTCAGCTACTGGGGAGGCTGAGGCAGGAAAATCACTTGAACTG A G ZYG11B Ensembl:ENSG00000162378 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs533989518 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 43082 RMVar_ID_43082 Human_SNP_ID_13510568 A-to-I Human chr1 + 52823198 52823198 52823198 ATTTAGGTCTGGATGCAGTGGCTCATGCTTGTAATCCCAGCACTTTGGGAAGCTGAAGCAGGAGG ATTTAGGTCTGGATGCAGTGGCTCATGCTTGTGATCCCAGCACTTTGGGAAGCTGAAGCAGGAGG A G ZYG11B Ensembl:ENSG00000162378 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-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 43083 RMVar_ID_43083 Human_SNP_ID_13510577 A-to-I Human chr1 + 52823225 52823225 52823225 CTTGTAATCCCAGCACTTTGGGAAGCTGAAGCAGGAGGATTGCTTGAGCCCAGAAGTTCAAGACT CTTGTAATCCCAGCACTTTGGGAAGCTGAAGCGGGAGGATTGCTTGAGCCCAGAAGTTCAAGACT A G ZYG11B Ensembl:ENSG00000162378 Protein coding 3'UTR GSE38233;GSE99789;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;esophageal squamous carcinoma cells,EC109;ASD brains,temporal_cortex;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29796672,30559470,31158229,31158229,31158229 RNA-Seq:(High) rs1129807 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 43084 RMVar_ID_43084 Human_SNP_ID_13510581 A-to-I Human chr1 + 52823252 52823252 52823252 GAAGCAGGAGGATTGCTTGAGCCCAGAAGTTCAAGACTAGCCTGGGCAACATAGTGAGACTCGGT GAAGCAGGAGGATTGCTTGAGCCCAGAAGTTCGAGACTAGCCTGGGCAACATAGTGAGACTCGGT A G ZYG11B Ensembl:ENSG00000162378 Protein coding 3'UTR GSE38233;GSE100210;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,cerebellum - 24183664,29129909,30559470 RNA-Seq:(High) rs3177646 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 43085 RMVar_ID_43085 Human_SNP_ID_13510834 A-to-I Human chr1 + 52824180 52824179 52824181 AAACTTCCTACTTTTTTTCTTTTTGTAGAGACAGAGTTTCACTCTGTCGCCCAAGCTGGAGTGCA AAACTTCCTACTTTTTTTCTTTTTGTAGAGAC__AGTTTCACTCTGTCGCCCAAGCTGGAGTGCA CAG C ZYG11B Ensembl:ENSG00000162378 Protein coding 3'UTR GSE38233;GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;ASD brains,frontal_cortex;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,30559470,31158229,31158229 RNA-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 43086 RMVar_ID_43086 Human_SNP_ID_13511202 A-to-I Human chr1 + 52825698 52825694 52825698 AAAAAAAAAGCGAGAGAGAGAGATGGTGTCTCACTGTGTTGCCCAGGCTGGTCTCGAACTCCTGG AAAAAAAAAGCGAGAGAGAGAGATGGTGT____CTGTGTTGCCCAGGCTGGTCTCGAACTCCTGG TCTCA T ZYG11B Ensembl:ENSG00000162378 Protein coding 3'UTR GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1360380566 Functional Loss DEL dbSNP153 30..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 43087 RMVar_ID_43087 Human_SNP_ID_13511206 A-to-I Human chr1 + 52825698 52825698 52825698 AAAAAAAAAGCGAGAGAGAGAGATGGTGTCTCACTGTGTTGCCCAGGCTGGTCTCGAACTCCTGG AAAAAAAAAGCGAGAGAGAGAGATGGTGTCTCGCTGTGTTGCCCAGGCTGGTCTCGAACTCCTGG A G ZYG11B Ensembl:ENSG00000162378 Protein coding 3'UTR GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1558147925 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 43088 RMVar_ID_43088 Human_SNP_ID_13511220 A-to-I Human chr1 + 52825735 52825735 52825735 GTTGCCCAGGCTGGTCTCGAACTCCTGGCCTCAAGTGACTTTCCCACCTCAGCTTCCCAAAGTGC GTTGCCCAGGCTGGTCTCGAACTCCTGGCCTCCAGTGACTTTCCCACCTCAGCTTCCCAAAGTGC A C ZYG11B Ensembl:ENSG00000162378 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,29129909,29796672,31158229,32596459 RNA-Seq:(High) rs1164199941 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26381370 RMVar_hsa_circ_97549,RMVar_hsa_circ_133045,RMVar_hsa_circ_90122,RMVar_hsa_circ_127307,RMVar_hsa_circ_133051,RMVar_hsa_circ_133053 43089 RMVar_ID_43089 Human_SNP_ID_13511223 A-to-I Human chr1 + 52825748 52825748 52825748 GTCTCGAACTCCTGGCCTCAAGTGACTTTCCCACCTCAGCTTCCCAAAGTGCTGGAATCACAGGC GTCTCGAACTCCTGGCCTCAAGTGACTTTCCCCCCTCAGCTTCCCAAAGTGCTGGAATCACAGGC A C ZYG11B Ensembl:ENSG00000162378 Protein coding 3'UTR GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;ASD brains,frontal_cortex;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,30559470,31158229,31158229,31158229,32596459,32596459 RNA-Seq:(High) rs947685461 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26381370 RMVar_hsa_circ_97549,RMVar_hsa_circ_133045,RMVar_hsa_circ_90122,RMVar_hsa_circ_127307,RMVar_hsa_circ_133051,RMVar_hsa_circ_133053 43090 RMVar_ID_43090 Human_SNP_ID_13511225 A-to-I Human chr1 + 52825753 52825753 52825753 GAACTCCTGGCCTCAAGTGACTTTCCCACCTCAGCTTCCCAAAGTGCTGGAATCACAGGCATGAG GAACTCCTGGCCTCAAGTGACTTTCCCACCTCTGCTTCCCAAAGTGCTGGAATCACAGGCATGAG A T ZYG11B Ensembl:ENSG00000162378 Protein coding 3'UTR GSE47997;GSE38233;GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,24183664,29129909,29796672,31158229,31158229,31158229,32596459,32596459 RNA-Seq:(High) rs1262737954 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26388217 RMVar_hsa_circ_97549,RMVar_hsa_circ_133045,RMVar_hsa_circ_90122,RMVar_hsa_circ_127307,RMVar_hsa_circ_133051,RMVar_hsa_circ_133053 43091 RMVar_ID_43091 Human_SNP_ID_13520801 A-to-I Human chr1 + 52861581 52861581 52861581 CAAAAATTTGGTGGGCGTGGTGGCGCACTCCTATAGTCCCAGCTACTTGGGAGACTGAGGCAGGA CAAAAATTTGGTGGGCGTGGTGGCGCACTCCTGTAGTCCCAGCTACTTGGGAGACTGAGGCAGGA A G ZYG11A Ensembl:ENSG00000203995 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs779275482 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24711225 RMVar_hsa_circ_1080,RMVar_hsa_circ_319975,RMVar_hsa_circ_110685,RMVar_hsa_circ_348232,RMVar_hsa_circ_133058,RMVar_hsa_circ_120907,RMVar_hsa_circ_52442,RMVar_hsa_circ_79045,RMVar_hsa_circ_283393,RMVar_hsa_circ_133061,RMVar_hsa_circ_320351,RMVar_hsa_circ_133062,RMVar_hsa_circ_41382,RMVar_hsa_circ_298575,RMVar_hsa_circ_359838,RMVar_hsa_circ_329154,RMVar_hsa_circ_270977,RMVar_hsa_circ_133063,RMVar_hsa_circ_133065,RMVar_hsa_circ_33720,RMVar_hsa_circ_133066,RMVar_hsa_circ_133064 43092 RMVar_ID_43092 Human_SNP_ID_13520802 A-to-I Human chr1 + 52861583 52861583 52861583 AAAATTTGGTGGGCGTGGTGGCGCACTCCTATAGTCCCAGCTACTTGGGAGACTGAGGCAGGAGA AAAATTTGGTGGGCGTGGTGGCGCACTCCTATCGTCCCAGCTACTTGGGAGACTGAGGCAGGAGA A C ZYG11A Ensembl:ENSG00000203995 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1462139226 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1080,RMVar_hsa_circ_319975,RMVar_hsa_circ_110685,RMVar_hsa_circ_348232,RMVar_hsa_circ_133058,RMVar_hsa_circ_120907,RMVar_hsa_circ_52442,RMVar_hsa_circ_79045,RMVar_hsa_circ_283393,RMVar_hsa_circ_133061,RMVar_hsa_circ_320351,RMVar_hsa_circ_133062,RMVar_hsa_circ_41382,RMVar_hsa_circ_298575,RMVar_hsa_circ_359838,RMVar_hsa_circ_329154,RMVar_hsa_circ_270977,RMVar_hsa_circ_133063,RMVar_hsa_circ_133065,RMVar_hsa_circ_33720,RMVar_hsa_circ_133066,RMVar_hsa_circ_133064 43093 RMVar_ID_43093 Human_SNP_ID_13522719 A-to-I Human chr1 + 52869035 52869035 52869035 TTTTGTATTTTTAGTAGAGACAGAGTTTCACTATGTTGGTCAGGCTGGTCTCCTGACCTTGTGAT TTTTGTATTTTTAGTAGAGACAGAGTTTCACTGTGTTGGTCAGGCTGGTCTCCTGACCTTGTGAT A G ZYG11A Ensembl:ENSG00000203995 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs530374964 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1080,RMVar_hsa_circ_120907,RMVar_hsa_circ_52442,RMVar_hsa_circ_79045,RMVar_hsa_circ_133061,RMVar_hsa_circ_41382,RMVar_hsa_circ_298575,RMVar_hsa_circ_359838,RMVar_hsa_circ_329154,RMVar_hsa_circ_133063,RMVar_hsa_circ_133065,RMVar_hsa_circ_133064,RMVar_hsa_circ_271111,RMVar_hsa_circ_374721,RMVar_hsa_circ_97874,RMVar_hsa_circ_22438,RMVar_hsa_circ_133068,RMVar_hsa_circ_133069,RMVar_hsa_circ_133070,RMVar_hsa_circ_22258,RMVar_hsa_circ_81644,RMVar_hsa_circ_133074,RMVar_hsa_circ_46718 43094 RMVar_ID_43094 Human_SNP_ID_13523894 A-to-I Human chr1 + 52872313 52872313 52872313 TTTAGTATAGATGAGGTTTCGCCATGTTGGCCAGTCTGGTCTCGAACTCCTGACCTCAGGTAATC TTTAGTATAGATGAGGTTTCGCCATGTTGGCCTGTCTGGTCTCGAACTCCTGACCTCAGGTAATC A T ZYG11A Ensembl:ENSG00000203995 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1457368201 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1080,RMVar_hsa_circ_120907,RMVar_hsa_circ_52442,RMVar_hsa_circ_79045,RMVar_hsa_circ_133061,RMVar_hsa_circ_41382,RMVar_hsa_circ_298575,RMVar_hsa_circ_359838,RMVar_hsa_circ_329154,RMVar_hsa_circ_133063,RMVar_hsa_circ_133065,RMVar_hsa_circ_133064,RMVar_hsa_circ_271111,RMVar_hsa_circ_374721,RMVar_hsa_circ_97874,RMVar_hsa_circ_22438,RMVar_hsa_circ_133068,RMVar_hsa_circ_133069,RMVar_hsa_circ_133070,RMVar_hsa_circ_22258,RMVar_hsa_circ_81644,RMVar_hsa_circ_133074,RMVar_hsa_circ_46718 43095 RMVar_ID_43095 Human_SNP_ID_13525414 A-to-I Human chr1 + 52878661 52878661 52878661 CCGTTTATCCTAATTAGAACTCAAACTCGGCCAGGCACGGTGGTTCATGCCTGTAATCCCAGCAC CCGTTTATCCTAATTAGAACTCAAACTCGGCCGGGCACGGTGGTTCATGCCTGTAATCCCAGCAC A G ZYG11A Ensembl:ENSG00000203995 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041269634 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5840660,Human_RBP_ID_11032577 RMVar_hsa_circ_1080,RMVar_hsa_circ_120907,RMVar_hsa_circ_133061,RMVar_hsa_circ_298575,RMVar_hsa_circ_359838,RMVar_hsa_circ_133063,RMVar_hsa_circ_271111,RMVar_hsa_circ_374721,RMVar_hsa_circ_6275,RMVar_hsa_circ_133069,RMVar_hsa_circ_133070,RMVar_hsa_circ_22258,RMVar_hsa_circ_81644,RMVar_hsa_circ_133074,RMVar_hsa_circ_377490,RMVar_hsa_circ_353215,RMVar_hsa_circ_326200,RMVar_hsa_circ_133076,RMVar_hsa_circ_133077,RMVar_hsa_circ_133080,RMVar_hsa_circ_372220,RMVar_hsa_circ_133075,RMVar_hsa_circ_273458,RMVar_hsa_circ_133079 43096 RMVar_ID_43096 Human_SNP_ID_13525465 A-to-I Human chr1 + 52878845 52878845 52878845 CCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATTGCTTGAACCTGGGAGGTAGAGATT CCTGTAATCCCAGCTACTTGGGAGGCTGAGGCGGGAGAATTGCTTGAACCTGGGAGGTAGAGATT A G ZYG11A Ensembl:ENSG00000203995 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs991036512 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1080,RMVar_hsa_circ_120907,RMVar_hsa_circ_133061,RMVar_hsa_circ_298575,RMVar_hsa_circ_359838,RMVar_hsa_circ_133063,RMVar_hsa_circ_271111,RMVar_hsa_circ_374721,RMVar_hsa_circ_6275,RMVar_hsa_circ_133069,RMVar_hsa_circ_133070,RMVar_hsa_circ_22258,RMVar_hsa_circ_81644,RMVar_hsa_circ_133074,RMVar_hsa_circ_377490,RMVar_hsa_circ_353215,RMVar_hsa_circ_326200,RMVar_hsa_circ_133076,RMVar_hsa_circ_133077,RMVar_hsa_circ_133080,RMVar_hsa_circ_372220,RMVar_hsa_circ_133075,RMVar_hsa_circ_273458,RMVar_hsa_circ_133079 43097 RMVar_ID_43097 Human_SNP_ID_13526690 A-to-I Human chr1 + 52883610 52883610 52883610 CACCACACCTAGCTAACTTTTGTACTTTTAGTAGTGACAGGGTTTCACCATGTTGGCCAGGCTAG CACCACACCTAGCTAACTTTTGTACTTTTAGTGGTGACAGGGTTTCACCATGTTGGCCAGGCTAG A G ZYG11A Ensembl:ENSG00000203995 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs915306153 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1080,RMVar_hsa_circ_120907,RMVar_hsa_circ_133061,RMVar_hsa_circ_298575,RMVar_hsa_circ_374721,RMVar_hsa_circ_6275,RMVar_hsa_circ_133070,RMVar_hsa_circ_81644,RMVar_hsa_circ_133074,RMVar_hsa_circ_377490,RMVar_hsa_circ_353215,RMVar_hsa_circ_133076,RMVar_hsa_circ_133080,RMVar_hsa_circ_372220,RMVar_hsa_circ_133075 43098 RMVar_ID_43098 Human_SNP_ID_13526714 A-to-I Human chr1 + 52883679 52883679 52883679 AAACTCCTGACCTCAAGGGATCTGCCCACCTCAGCCTCCAAAAGTGCTGGGATTACATGCATGAG AAACTCCTGACCTCAAGGGATCTGCCCACCTCTGCCTCCAAAAGTGCTGGGATTACATGCATGAG A T ZYG11A Ensembl:ENSG00000203995 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1361907015 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1080,RMVar_hsa_circ_120907,RMVar_hsa_circ_133061,RMVar_hsa_circ_298575,RMVar_hsa_circ_374721,RMVar_hsa_circ_6275,RMVar_hsa_circ_133070,RMVar_hsa_circ_81644,RMVar_hsa_circ_133074,RMVar_hsa_circ_377490,RMVar_hsa_circ_353215,RMVar_hsa_circ_133076,RMVar_hsa_circ_133080,RMVar_hsa_circ_372220,RMVar_hsa_circ_133075 43099 RMVar_ID_43099 Human_SNP_ID_13527831 A-to-I Human chr1 + 52887654 52887654 52887654 GCTGGGATTACAGCACTTTGGGAGGCCGAGGCAGGAGATCGCTTGAGGCCAGGAGTTTGAGACCA GCTGGGATTACAGCACTTTGGGAGGCCGAGGCGGGAGATCGCTTGAGGCCAGGAGTTTGAGACCA A G ZYG11A Ensembl:ENSG00000203995 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1415751252 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23402311 RMVar_hsa_circ_377490,RMVar_hsa_circ_133075,RMVar_hsa_circ_133083 43100 RMVar_ID_43100 Human_SNP_ID_13528554 A-to-I Human chr1 + 52890486 52890486 52890486 GTCTCAAAGTCCTGACCTTAGATGTTCGCCTCAGCCTCCCAGAGTGCTGGGATTACAGGCATGAG GTCTCAAAGTCCTGACCTTAGATGTTCGCCTCTGCCTCCCAGAGTGCTGGGATTACAGGCATGAG A T ZYG11A Ensembl:ENSG00000203995 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1316134808 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11033013 RMVar_hsa_circ_377490,RMVar_hsa_circ_133075,RMVar_hsa_circ_133083 43101 RMVar_ID_43101 Human_SNP_ID_13529313 A-to-I Human chr1 + 52893515 52893515 52893515 GGCTGGGTATGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGTGGATTGTC GGCTGGGTATGGTGGCTCACGCCTGTAATCCCGGCACTTTGGGAGGCCAAGGCAGGTGGATTGTC A G ZYG11A Ensembl:ENSG00000203995 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1352204109 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8314451,Human_RBP_ID_11033137 43102 RMVar_ID_43102 Human_SNP_ID_13529334 A-to-I Human chr1 + 52893600 52893600 52893600 CAGCCTTGCCAACGTGGTAAAACTCCGTCTCTACCAAAAAATACAAAAATTAGCTGAGCGTGGTG CAGCCTTGCCAACGTGGTAAAACTCCGTCTCTGCCAAAAAATACAAAAATTAGCTGAGCGTGGTG A G ZYG11A Ensembl:ENSG00000203995 Protein coding 3'UTR GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs1163963267 Functional Loss SNV dbSNP153 33..33 33 - - - 43103 RMVar_ID_43103 Human_SNP_ID_13529336 A-to-I Human chr1 + 52893607 52893607 52893607 GCCAACGTGGTAAAACTCCGTCTCTACCAAAAAATACAAAAATTAGCTGAGCGTGGTGGTGTGCA GCCAACGTGGTAAAACTCCGTCTCTACCAAAACATACAAAAATTAGCTGAGCGTGGTGGTGTGCA A C ZYG11A Ensembl:ENSG00000203995 Protein coding 3'UTR GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs998612565 Functional Loss SNV dbSNP153 33..33 33 - - - 43104 RMVar_ID_43104 Human_SNP_ID_13529339 A-to-I Human chr1 + 52893619 52893619 52893619 AAACTCCGTCTCTACCAAAAAATACAAAAATTAGCTGAGCGTGGTGGTGTGCACCTTTACTCCTA AAACTCCGTCTCTACCAAAAAATACAAAAATTTGCTGAGCGTGGTGGTGTGCACCTTTACTCCTA A T ZYG11A Ensembl:ENSG00000203995 Protein coding 3'UTR GSE38233;GSE100210;GSE99789 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 24183664,29129909,29796672 RNA-Seq:(High) rs1368958280 Functional Loss SNV dbSNP153 33..33 33 - - - 43105 RMVar_ID_43105 Human_SNP_ID_13529450 A-to-I Human chr1 + 52893953 52893953 52893953 CCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCACATGCCGCCACGCCCGGCTAATTTTTGT CCTGCCTCAGCCTCCTGAGTAGCTGGGACTACGGGCACATGCCGCCACGCCCGGCTAATTTTTGT A G ZYG11A Ensembl:ENSG00000203995 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1394608058 Functional Loss SNV dbSNP153 33..33 33 - - - 43106 RMVar_ID_43106 Human_SNP_ID_13529451 A-to-I Human chr1 + 52893957 52893957 52893957 CCTCAGCCTCCTGAGTAGCTGGGACTACAGGCACATGCCGCCACGCCCGGCTAATTTTTGTATTT CCTCAGCCTCCTGAGTAGCTGGGACTACAGGCGCATGCCGCCACGCCCGGCTAATTTTTGTATTT A G ZYG11A Ensembl:ENSG00000203995 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1035158646 Functional Loss SNV dbSNP153 33..33 33 - - - 43107 RMVar_ID_43107 Human_SNP_ID_13529463 A-to-I Human chr1 + 52893986 52893986 52893986 GGCACATGCCGCCACGCCCGGCTAATTTTTGTATTTTTTAGTAGAGACAGGGTTTCACCATATTG GGCACATGCCGCCACGCCCGGCTAATTTTTGTGTTTTTTAGTAGAGACAGGGTTTCACCATATTG A G ZYG11A Ensembl:ENSG00000203995 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs933894851 Functional Loss SNV dbSNP153 33..33 33 - - - 43108 RMVar_ID_43108 Human_SNP_ID_13529486 A-to-I Human chr1 + 52894072 52894072 52894072 TGACCTCGTGATCCACCCGTCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGTCACTGCAC TGACCTCGTGATCCACCCGTCTCGGCCTCCCAGAGTGCTGGGATTACAGGTGTGAGTCACTGCAC A G ZYG11A Ensembl:ENSG00000203995 Protein coding 3'UTR GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831 esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line - 29796672,31158229,32596459 RNA-Seq:(High) rs1000243887 Functional Loss SNV dbSNP153 33..33 33 - - - 43109 RMVar_ID_43109 Human_SNP_ID_13531147 A-to-I Human chr1 + 52901066 52901066 52901066 TGTAGTCTCAGCTACTCAGTAGTCTTAGGTGGAAGGATCACTTGGGCCTGAGAGGTCAATGCTCC TGTAGTCTCAGCTACTCAGTAGTCTTAGGTGGGAGGATCACTTGGGCCTGAGAGGTCAATGCTCC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1045557222 Functional Loss SNV dbSNP153 33..33 33 - - - 43110 RMVar_ID_43110 Human_SNP_ID_13531429 A-to-I Human chr1 + 52902236 52902236 52902236 TGGAGTGCAGTGGTGCGATCTCGGCTCACTGCAACCTCCACCTCCCAGACTCAAGTGATTCTCGT TGGAGTGCAGTGGTGCGATCTCGGCTCACTGCTACCTCCACCTCCCAGACTCAAGTGATTCTCGT A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs944042374 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24711644 43111 RMVar_ID_43111 Human_SNP_ID_13534268 A-to-I Human chr1 - 52912833 52912833 52912833 AAAAATACAAAATTAGCCGGGCGTGGTGGCACATGCTGTAATCCCAGCTACTCCGGAGGCTGAGG AAAAATACAAAATTAGCCGGGCGTGGTGGCACGTGCTGTAATCCCAGCTACTCCGGAGGCTGAGG T C ECHDC2 Ensembl:ENSG00000121310 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1039323193 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_71437,Human_Splice_Rec_71500,Human_Splice_Rec_71501,Human_Splice_Rec_71511 43112 RMVar_ID_43112 Human_SNP_ID_13535169 A-to-I Human chr1 - 52917056 52917056 52917056 ACCACGCCTGGCTAATTTTTGTCTTTTTAGTAAAGACGGGGTTTCACCATGTTGGTCAGGCTGGT ACCACGCCTGGCTAATTTTTGTCTTTTTAGTAGAGACGGGGTTTCACCATGTTGGTCAGGCTGGT T C ECHDC2 Ensembl:ENSG00000121310 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs995547843 Functional Loss SNV dbSNP153 33..33 33 - - - 43113 RMVar_ID_43113 Human_SNP_ID_13535661 A-to-I Human chr1 - 52919086 52919086 52919086 TGAAACTGTTCCACCTCAGATCATCAGGCATTAGATTCTCATAAGGAGCTCGCAACAACCTAGAT TGAAACTGTTCCACCTCAGATCATCAGGCATTGGATTCTCATAAGGAGCTCGCAACAACCTAGAT T C ECHDC2 Ensembl:ENSG00000121310 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs779225160 Functional Loss SNV dbSNP153 33..33 33 - - - 43114 RMVar_ID_43114 Human_SNP_ID_13537998 A-to-I Human chr1 + 52928647 52928647 52928647 TACTAAAAATACGAAAATTAGTCGGGCATGGTAGCACACGCCAGCTACTCGGGAGGCTGAGGTGG TACTAAAAATACGAAAATTAGTCGGGCATGGTTGCACACGCCAGCTACTCGGGAGGCTGAGGTGG A T SCP2 Ensembl:ENSG00000116171 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs955906324 Functional Loss SNV dbSNP153 33..33 33 - - - 43115 RMVar_ID_43115 Human_SNP_ID_13552921 A-to-I Human chr1 - 52993367 52993367 52993367 ACACAGGAAGAAGGACGGCAGTTAGCACGGCAACTTAAGGTAACATACATGGAGGCATCAGCAAA ACACAGGAAGAAGGACGGCAGTTAGCACGGCAGCTTAAGGTAACATACATGGAGGCATCAGCAAA T C RRAS2P1 Ensembl:ENSG00000236360 Pseudogene exon GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs878879572 Functional Loss SNV dbSNP153 33..33 33 - - - 43116 RMVar_ID_43116 Human_SNP_ID_13558466 A-to-I Human chr1 + 53018577 53018577 53018577 CAGCCTGGACAACATGGCGAAACCCCCTCTCTACTAAAAATCAAAAATTAGCCAGGCGTGGTAGC CAGCCTGGACAACATGGCGAAACCCCCTCTCTCCTAAAAATCAAAAATTAGCCAGGCGTGGTAGC A C SCP2 Ensembl:ENSG00000116171 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1458808710 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_350017,RMVar_hsa_circ_71708,RMVar_hsa_circ_364953,RMVar_hsa_circ_369023,RMVar_hsa_circ_133091,RMVar_hsa_circ_352974,RMVar_hsa_circ_351838 43117 RMVar_ID_43117 Human_SNP_ID_13612480 A-to-I Human chr1 - 53230472 53230472 53230472 TCAGGGTTACAGTGAGCTATGATCCTACTACTATACTTCAGCTTCAGTGACAGAGTGAGATCCTG TCAGGGTTACAGTGAGCTATGATCCTACTACTGTACTTCAGCTTCAGTGACAGAGTGAGATCCTG T C MAGOH Ensembl:ENSG00000162385 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1470157633 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5841189 RMVar_hsa_circ_111851,RMVar_hsa_circ_315264,RMVar_hsa_circ_133095 43118 RMVar_ID_43118 Human_SNP_ID_13628387 A-to-I Human chr1 - 53301833 53301833 53301833 CTATAGACTCTCTGAAGGAAGGTCCACCTCTCACTTTTTCCTTTGCTTGCACAGCATTCGGGATG CTATAGACTCTCTGAAGGAAGGTCCACCTCTCCCTTTTTCCTTTGCTTGCACAGCATTCGGGATG T G LRP8 Ensembl:ENSG00000157193 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1191023947 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15517,RMVar_hsa_circ_268781 43119 RMVar_ID_43119 Human_SNP_ID_13633630 A-to-I Human chr1 - 53324202 53324202 53324202 AGAGCTGTTGGCTCGTCCCTGAGGAGCTCTTTATTAAACCTGGGATGGAGGGGTGATAGGTGCTG AGAGCTGTTGGCTCGTCCCTGAGGAGCTCTTTGTTAAACCTGGGATGGAGGGGTGATAGGTGCTG T C LRP8 Ensembl:ENSG00000157193 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941842643 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557907 RMVar_hsa_circ_15517,RMVar_hsa_circ_268781,RMVar_hsa_circ_133108 43120 RMVar_ID_43120 Human_SNP_ID_13730569 A-to-I Human chr1 - 53722829 53722829 53722829 TGCACCTGGCCTACTCTTTTTTTTTTTTTTTGAGACGGGGTCTCACTGTCGCCCAGGGTGGAGTG TGCACCTGGCCTACTCTTTTTTTTTTTTTTTGTGACGGGGTCTCACTGTCGCCCAGGGTGGAGTG T A GLIS1 Ensembl:ENSG00000174332 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1255712462 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48514 43121 RMVar_ID_43121 Human_SNP_ID_13742676 A-to-I Human chr1 - 53776243 53776243 53776243 CATATAAGAGGAATTTCAGGACCGGGCGCGGTAGCTCACACCTGTAATCCCAGCACTTTGGGAAA CATATAAGAGGAATTTCAGGACCGGGCGCGGTTGCTCACACCTGTAATCCCAGCACTTTGGGAAA T A NDC1 Ensembl:ENSG00000058804 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs921572233 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11035028 RMVar_hsa_circ_267919,RMVar_hsa_circ_133111,RMVar_hsa_circ_103866,RMVar_hsa_circ_316291,RMVar_hsa_circ_348703,RMVar_hsa_circ_368678,RMVar_hsa_circ_316015,RMVar_hsa_circ_51243,RMVar_hsa_circ_267413,RMVar_hsa_circ_23919,RMVar_hsa_circ_133112 43122 RMVar_ID_43122 Human_SNP_ID_13746973 A-to-I Human chr1 - 53794104 53794100 53794104 GGGTGTGGTGGTGCATTCCTGTAGTCCTAGCTACTTGGGAGGCTGAGGTAGGAGAATCACCTGAG GGGTGTGGTGGTGCATTCCTGTAGTCCTAGCT____GGGAGGCTGAGGTAGGAGAATCACCTGAG CAAGT C NDC1 Ensembl:ENSG00000058804 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1032890719 Functional Loss DEL dbSNP153 33..36 33 - - - 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 43123 RMVar_ID_43123 Human_SNP_ID_13746995 A-to-I Human chr1 - 53794199 53794199 53794199 TGCCACAGTGGGAACATTGCTTGAGCCCGGGAATTCGAGACCAGCATGGGCAACATGGCAAAACC TGCCACAGTGGGAACATTGCTTGAGCCCGGGAGTTCGAGACCAGCATGGGCAACATGGCAAAACC T C NDC1 Ensembl:ENSG00000058804 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs940561102 Functional Loss SNV dbSNP153 33..33 33 - - - 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 43124 RMVar_ID_43124 Human_SNP_ID_13747100 A-to-I Human chr1 - 53794652 53794652 53794652 TTGCCCAGGCTGATCTCAAACTCTTGGCCTCAAGCAGTCATCCTGCCTGAGCCTCATAAAGTGTT TTGCCCAGGCTGATCTCAAACTCTTGGCCTCAGGCAGTCATCCTGCCTGAGCCTCATAAAGTGTT T C NDC1 Ensembl:ENSG00000058804 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1034129898 Functional Loss SNV dbSNP153 33..33 33 - - - 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 43125 RMVar_ID_43125 Human_SNP_ID_13747129 A-to-I Human chr1 - 53794753 53794753 53794753 CTCCCACCTCAGCCTCCTGAGTAGCTGGGACTACAGGTGCCTGCCACCATGCCTGCCTAATTTTT CTCCCACCTCAGCCTCCTGAGTAGCTGGGACTGCAGGTGCCTGCCACCATGCCTGCCTAATTTTT T C NDC1 Ensembl:ENSG00000058804 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1045441572 Functional Loss SNV dbSNP153 33..33 33 - - - 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 43126 RMVar_ID_43126 Human_SNP_ID_13762462 A-to-I Human chr1 - 53858766 53858766 53858766 GCTTGGCATGGTGGCATGCTCCTGTAGTCCCAACTAGTTGGGAGGCTGGGGTTGGAGGATCACTT GCTTGGCATGGTGGCATGCTCCTGTAGTCCCAGCTAGTTGGGAGGCTGGGGTTGGAGGATCACTT T C YIPF1 Ensembl:ENSG00000058799 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs777337786 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_133147,RMVar_hsa_circ_373469 43127 RMVar_ID_43127 Human_SNP_ID_13777241 A-to-I Human chr1 - 53922212 53922212 53922212 TTTCGTATTTTTAGTAGAGACAGGGTTTCTCCATGTTGGTTAGGCTGTTCTCAAACTCCCAACCT TTTCGTATTTTTAGTAGAGACAGGGTTTCTCCGTGTTGGTTAGGCTGTTCTCAAACTCCCAACCT T C HSPB11 Ensembl:ENSG00000081870 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1056821858 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_133157,RMVar_hsa_circ_117783 43128 RMVar_ID_43128 Human_SNP_ID_13778260 A-to-I Human chr1 - 53926411 53926411 53926411 AGCTAGGCTCACGCCCATAATCCCAGCATTTTAGGAGGCTGAGGTGGGCGGATCGTTTGATCTCA AGCTAGGCTCACGCCCATAATCCCAGCATTTTGGGAGGCTGAGGTGGGCGGATCGTTTGATCTCA T C HSPB11 Ensembl:ENSG00000081870 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1398253014 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_133157,RMVar_hsa_circ_117783,RMVar_hsa_circ_133158,RMVar_hsa_circ_344604,RMVar_hsa_circ_378164 43129 RMVar_ID_43129 Human_SNP_ID_13778372 A-to-I Human chr1 - 53926860 53926860 53926860 AAATTAGCCAGGGATGGTGACATGTGCCTGTAATCGTAGCTACTTGGGAGGCTGAGATGGAAGGA AAATTAGCCAGGGATGGTGACATGTGCCTGTATTCGTAGCTACTTGGGAGGCTGAGATGGAAGGA T A HSPB11 Ensembl:ENSG00000081870 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985007672 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_133157,RMVar_hsa_circ_117783,RMVar_hsa_circ_133158,RMVar_hsa_circ_344604,RMVar_hsa_circ_378164 43130 RMVar_ID_43130 Human_SNP_ID_13778411 A-to-I Human chr1 - 53926998 53926998 53926998 TGTGGGGCCTGGGCACAGTGGCTCATGCCTGTAATCCCAACACTTTGGGAGGCTGAGGGAGGAGG TGTGGGGCCTGGGCACAGTGGCTCATGCCTGTGATCCCAACACTTTGGGAGGCTGAGGGAGGAGG T C HSPB11 Ensembl:ENSG00000081870 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1181303273 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_133157,RMVar_hsa_circ_117783,RMVar_hsa_circ_133158,RMVar_hsa_circ_344604,RMVar_hsa_circ_378164 43131 RMVar_ID_43131 Human_SNP_ID_13780759 A-to-I Human chr1 - 53937257 53937257 53937257 AAAAAATTAGTCAGTTGTGGTGGCGTGCACCTATAGTCCCAGCTCCTCGGGAGGCTGAGGCACGA AAAAAATTAGTCAGTTGTGGTGGCGTGCACCTGTAGTCCCAGCTCCTCGGGAGGCTGAGGCACGA T C HSPB11 Ensembl:ENSG00000081870 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432985323 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_133157,RMVar_hsa_circ_117783,RMVar_hsa_circ_133158,RMVar_hsa_circ_344604,RMVar_hsa_circ_133159 43132 RMVar_ID_43132 Human_SNP_ID_13780764 A-to-I Human chr1 - 53937281 53937281 53937281 AACTCTGTCTCTATTAAAAATACCAAAAAATTAGTCAGTTGTGGTGGCGTGCACCTATAGTCCCA AACTCTGTCTCTATTAAAAATACCAAAAAATTCGTCAGTTGTGGTGGCGTGCACCTATAGTCCCA T G HSPB11 Ensembl:ENSG00000081870 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1297709757 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_133157,RMVar_hsa_circ_117783,RMVar_hsa_circ_133158,RMVar_hsa_circ_344604,RMVar_hsa_circ_133159 43133 RMVar_ID_43133 Human_SNP_ID_13782550 A-to-I Human chr1 - 53944563 53944563 53944563 CTCGCCTCACTGAGCCTCCGCTTCCTGGGTTCAGGAGCTTCTCCTGCCTCAGCCTCCGGAGTAGC CTCGCCTCACTGAGCCTCCGCTTCCTGGGTTCGGGAGCTTCTCCTGCCTCAGCCTCCGGAGTAGC T C HSPB11 Ensembl:ENSG00000081870 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1003808595 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_133157,RMVar_hsa_circ_117783 43134 RMVar_ID_43134 Human_SNP_ID_13804627 A-to-I Human chr1 - 54033039 54033039 54033039 CCTATAGTCCTAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAGCCCAGGAGTTCAAGGCC CCTATAGTCCTAGCTACTCAGGAGGCTGAGGCGGGAGAATCACTTGAGCCCAGGAGTTCAAGGCC T C TMEM59 Ensembl:ENSG00000116209 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs367931160 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101648,RMVar_hsa_circ_133167 43135 RMVar_ID_43135 Human_SNP_ID_13804629 A-to-I Human chr1 - 54033068 54033068 54033068 GAAAAATTAGCTGGGCATGGTGGTGCATGCCTATAGTCCTAGCTACTCAGGAGGCTGAGGCAGGA GAAAAATTAGCTGGGCATGGTGGTGCATGCCTGTAGTCCTAGCTACTCAGGAGGCTGAGGCAGGA T C TMEM59 Ensembl:ENSG00000116209 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1237085762 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101648,RMVar_hsa_circ_133167 43136 RMVar_ID_43136 Human_SNP_ID_13804692 A-to-I Human chr1 - 54033239 54033238 54033239 AGAGATACATACGGACAGGCCTAGTGGCTCACACATGTATCCCAACACTTTGGGAGGCCAAGGTA AGAGATACATACGGACAGGCCTAGTGGCTCAC_CATGTATCCCAACACTTTGGGAGGCCAAGGTA GT G TMEM59,AL353898.3 Ensembl:ENSG00000116209,Ensembl:ENSG00000280378 Protein coding,Other intron,exon GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1431028139 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_17558517,Human_RBP_ID_18509496 RMVar_hsa_circ_101648,RMVar_hsa_circ_133167 43137 RMVar_ID_43137 Human_SNP_ID_13804693 A-to-I Human chr1 - 54033239 54033239 54033239 AGAGATACATACGGACAGGCCTAGTGGCTCACACATGTATCCCAACACTTTGGGAGGCCAAGGTA AGAGATACATACGGACAGGCCTAGTGGCTCACTCATGTATCCCAACACTTTGGGAGGCCAAGGTA T A TMEM59,AL353898.3 Ensembl:ENSG00000116209,Ensembl:ENSG00000280378 Protein coding,Other intron,exon GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs113066069 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17558517,Human_RBP_ID_18509496 RMVar_hsa_circ_101648,RMVar_hsa_circ_133167 43138 RMVar_ID_43138 Human_SNP_ID_13818648 A-to-I Human chr1 + 54096328 54096328 54096328 ACTGGTTGAAAATATTGAACGGGAAACGTTTCATCTCTGCTCCCGCCTCATTAATGGGCCGTACC ACTGGTTGAAAATATTGAACGGGAAACGTTTCGTCTCTGCTCCCGCCTCATTAATGGGCCGTACC A G TCEANC2 Ensembl:ENSG00000116205 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs753440249 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19384038,Human_RBP_ID_22145167,Human_RBP_ID_26866919 Human_Splice_Rec_73530,Human_Splice_Rec_73538,Human_Splice_Rec_73548,Human_Splice_Rec_73554 RMVar_hsa_circ_133175,RMVar_hsa_circ_79933,RMVar_hsa_circ_133174 43139 RMVar_ID_43139 Human_SNP_ID_13819326 A-to-I Human chr1 + 54099601 54099600 54099601 CCCTGTCTGTACTAAAAATACAAAAATTAGCCAGATATGATGGCAGGCGCCTGTAATCCCAGCTA CCCTGTCTGTACTAAAAATACAAAAATTAGCC_GATATGATGGCAGGCGCCTGTAATCCCAGCTA CA C TCEANC2 Ensembl:ENSG00000116205 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1194422608 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_79933,RMVar_hsa_circ_133174 43140 RMVar_ID_43140 Human_SNP_ID_13820441 A-to-I Human chr1 + 54104794 54104794 54104794 GAACTTCTGGCCTCAAGCAGTCCACCTGCCTCAGCTTCCCAAAGTGCTGGGATTACAGGCGTGAG GAACTTCTGGCCTCAAGCAGTCCACCTGCCTCGGCTTCCCAAAGTGCTGGGATTACAGGCGTGAG A G TCEANC2 Ensembl:ENSG00000116205 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1341647988 Functional Loss SNV dbSNP153 33..33 33 - - - 43141 RMVar_ID_43141 Human_SNP_ID_13820713 A-to-I Human chr1 + 54105899 54105899 54105899 CCTCGGCCTCCCAAAGTGCTGGGATTATAGACATGAATCACCACACCCGGCCAGCAAACTTTTTT CCTCGGCCTCCCAAAGTGCTGGGATTATAGACGTGAATCACCACACCCGGCCAGCAAACTTTTTT A G TCEANC2 Ensembl:ENSG00000116205 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs899457684 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11037422 43142 RMVar_ID_43142 Human_SNP_ID_13839606 A-to-I Human chr1 - 54180956 54180956 54180956 GCTGGAGTGCAGTGGCATGATCATGGTTCACTACAGCCCCAACCTCCTGGGCTCAAGCGATCCTC GCTGGAGTGCAGTGGCATGATCATGGTTCACTTCAGCCCCAACCTCCTGGGCTCAAGCGATCCTC T A CYB5RL,AL357673.1 Ensembl:ENSG00000215883,Ensembl:ENSG00000256407 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1038514341 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_368015 43143 RMVar_ID_43143 Human_SNP_ID_13848116 A-to-I Human chr1 + 54216261 54216261 54216261 ATACCACAGACCTGGACTGTAACGAGGGTGTCAAGAATTTGGCCTGGGTGGACTCAGACCAGCTC ATACCACAGACCTGGACTGTAACGAGGGTGTCTAGAATTTGGCCTGGGTGGACTCAGACCAGCTC A T MRPL37 Ensembl:ENSG00000116221 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1416356897 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18057,Human_RBP_ID_358496,Human_RBP_ID_1750724,Human_RBP_ID_4097799,Human_RBP_ID_11038097,Human_RBP_ID_23403170 Human_Splice_Rec_73707,Human_Splice_Rec_73719,Human_Splice_Rec_73731,Human_Splice_Rec_73745 Human_miRNA_ID_2781989,Human_miRNA_ID_2784957 RMVar_hsa_circ_104422,RMVar_hsa_circ_133179,RMVar_hsa_circ_280492,RMVar_hsa_circ_23760,RMVar_hsa_circ_87309,RMVar_hsa_circ_133181,RMVar_hsa_circ_133182,RMVar_hsa_circ_133185,RMVar_hsa_circ_115547,RMVar_hsa_circ_123075,RMVar_hsa_circ_133183,RMVar_hsa_circ_79865,RMVar_hsa_circ_133184 43144 RMVar_ID_43144 Human_SNP_ID_13851119 A-to-I Human chr1 - 54226926 54226926 54226926 ATGCAATAAAAAGGCCAAACTTTTTATTCCATAAAACAAGAAGGACAAAACTCTCAAAAATGTAT ATGCAATAAAAAGGCCAAACTTTTTATTCCATGAAACAAGAAGGACAAAACTCTCAAAAATGTAT T C SSBP3 Ensembl:ENSG00000157216 Protein coding exon GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1370211031 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_358550,Human_RBP_ID_979108,Human_RBP_ID_5842490,Human_RBP_ID_17219302,Human_RBP_ID_17336493,Human_RBP_ID_17453947,Human_RBP_ID_17754548,Human_RBP_ID_18929746,Human_RBP_ID_27596361 43145 RMVar_ID_43145 Human_SNP_ID_13851120 A-to-I Human chr1 - 54226926 54226926 54226926 ATGCAATAAAAAGGCCAAACTTTTTATTCCATAAAACAAGAAGGACAAAACTCTCAAAAATGTAT ATGCAATAAAAAGGCCAAACTTTTTATTCCATCAAACAAGAAGGACAAAACTCTCAAAAATGTAT T G SSBP3 Ensembl:ENSG00000157216 Protein coding exon GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1370211031 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_358550,Human_RBP_ID_979108,Human_RBP_ID_5842490,Human_RBP_ID_17219302,Human_RBP_ID_17336493,Human_RBP_ID_17453947,Human_RBP_ID_17754548,Human_RBP_ID_18929746,Human_RBP_ID_27596361 43146 RMVar_ID_43146 Human_SNP_ID_13853658 A-to-I Human chr1 - 54234408 54234408 54234408 AATTTTATTTGTTGTTGTAGAGATGAGGTCTCACTATGTTGCCCCTAATTTATTTTTTATTTTTT AATTTTATTTGTTGTTGTAGAGATGAGGTCTCGCTATGTTGCCCCTAATTTATTTTTTATTTTTT T C SSBP3 Ensembl:ENSG00000157216 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1469874900 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29296 43147 RMVar_ID_43147 Human_SNP_ID_13853680 A-to-I Human chr1 - 54234466 54234466 54234466 CTCCCACCACAGCTTCCTGAGTAGCTGGGACTACAGGCACGTGCCACCACACCCGGCTAATTTTA CTCCCACCACAGCTTCCTGAGTAGCTGGGACTGCAGGCACGTGCCACCACACCCGGCTAATTTTA T C SSBP3 Ensembl:ENSG00000157216 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1252739784 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29296 43148 RMVar_ID_43148 Human_SNP_ID_13853801 A-to-I Human chr1 - 54234896 54234896 54234896 TAAGCTGGGTACAGTGGTGTATGCCTGTAGTCAGCTACTCGGGAGGCTGAAGCGGGAGGATTGTT TAAGCTGGGTACAGTGGTGTATGCCTGTAGTCGGCTACTCGGGAGGCTGAAGCGGGAGGATTGTT T C SSBP3 Ensembl:ENSG00000157216 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1484201881 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29296 43149 RMVar_ID_43149 Human_SNP_ID_13860103 A-to-I Human chr1 - 54254993 54254993 54254993 CCCTGTCTCTACTAAAAATCCAAAAATTAGCCAGGCATGCTGGCGTGTGCCTGTAATCCCAGCTA CCCTGTCTCTACTAAAAATCCAAAAATTAGCCGGGCATGCTGGCGTGTGCCTGTAATCCCAGCTA T C SSBP3 Ensembl:ENSG00000157216 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1231936355 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5296,RMVar_hsa_circ_368793,RMVar_hsa_circ_133194,RMVar_hsa_circ_312718,RMVar_hsa_circ_369683,RMVar_hsa_circ_295687,RMVar_hsa_circ_29388,RMVar_hsa_circ_133192,RMVar_hsa_circ_133193 43150 RMVar_ID_43150 Human_SNP_ID_13860109 A-to-I Human chr1 - 54255012 54255012 54255012 CCTGGCCAACATGGTGAAACCCTGTCTCTACTAAAAATCCAAAAATTAGCCAGGCATGCTGGCGT CCTGGCCAACATGGTGAAACCCTGTCTCTACTGAAAATCCAAAAATTAGCCAGGCATGCTGGCGT T C SSBP3 Ensembl:ENSG00000157216 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1275467130 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24712665 RMVar_hsa_circ_5296,RMVar_hsa_circ_368793,RMVar_hsa_circ_133194,RMVar_hsa_circ_312718,RMVar_hsa_circ_369683,RMVar_hsa_circ_295687,RMVar_hsa_circ_29388,RMVar_hsa_circ_133192,RMVar_hsa_circ_133193 43151 RMVar_ID_43151 Human_SNP_ID_13882835 A-to-I Human chr1 - 54337770 54337770 54337770 TTTGAGGAGGCCGGGCATGGTGGCCCACGCCTATCATCCCAGCCCTTTGGGAGGCCAAGGCAGGT TTTGAGGAGGCCGGGCATGGTGGCCCACGCCTGTCATCCCAGCCCTTTGGGAGGCCAAGGCAGGT T C SSBP3 Ensembl:ENSG00000157216 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1463703389 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98880,RMVar_hsa_circ_29388,RMVar_hsa_circ_133195 43152 RMVar_ID_43152 Human_SNP_ID_13886674 A-to-I Human chr1 - 54352111 54352111 54352111 TTGTTTGTTTTGTAGAGATAGGGTCTCACTATATTGCCCAGTTAGGTCTTAAACTCCTGGCTTCA TTGTTTGTTTTGTAGAGATAGGGTCTCACTATGTTGCCCAGTTAGGTCTTAAACTCCTGGCTTCA T C SSBP3 Ensembl:ENSG00000157216 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs868056829 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98880,RMVar_hsa_circ_29388,RMVar_hsa_circ_133195 43153 RMVar_ID_43153 Human_SNP_ID_13933832 A-to-I Human chr1 - 54524868 54524868 54524868 GTCAGCATCCACTCCAGCTTCACTGCGTCAGCAGCAGACTTGCGGATCCCATCAGAGAGCTTCTC GTCAGCATCCACTCCAGCTTCACTGCGTCAGCGGCAGACTTGCGGATCCCATCAGAGAGCTTCTC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1286649220 Functional Loss SNV dbSNP153 33..33 33 - - - 43154 RMVar_ID_43154 Human_SNP_ID_13933839 A-to-I Human chr1 - 54524890 54524890 54524890 CTCTGCATTGAACATTCATTCTGTCAGCATCCACTCCAGCTTCACTGCGTCAGCAGCAGACTTGC CTCTGCATTGAACATTCATTCTGTCAGCATCCGCTCCAGCTTCACTGCGTCAGCAGCAGACTTGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1372344781 Functional Loss SNV dbSNP153 33..33 33 - - - 43155 RMVar_ID_43155 Human_SNP_ID_13933849 A-to-I Human chr1 - 54524935 54524935 54524935 AGTGCAGATCTGGAGTCCAGCCTCATGGCTGCACTACTTTCCATTCTCTGCATTGAACATTCATT AGTGCAGATCTGGAGTCCAGCCTCATGGCTGCGCTACTTTCCATTCTCTGCATTGAACATTCATT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1436568604 Functional Loss SNV dbSNP153 33..33 33 - - - 43156 RMVar_ID_43156 Human_SNP_ID_13984577 A-to-I Human chr1 + 54718481 54718481 54718481 ATGTTGCCCGGGCTGGTCTCGAAATTGGGCTCAAGTGATCCATCCGCCTCAGCCTCCCAAAGTAT ATGTTGCCCGGGCTGGTCTCGAAATTGGGCTCTAGTGATCCATCCGCCTCAGCCTCCCAAAGTAT A T TTC4,MROH7-TTC4 Ensembl:ENSG00000243725,Ensembl:ENSG00000271723 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1333266512 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268827,RMVar_hsa_circ_313788,RMVar_hsa_circ_57812 43157 RMVar_ID_43157 Human_SNP_ID_13994149 A-to-I Human chr1 - 54757236 54757236 54757236 CACTGAGAAGTTGGGCTGAGAGTATGGGGAAAAGAATCAAGAGACCTGACTGCCGCCAACTCACT CACTGAGAAGTTGGGCTGAGAGTATGGGGAAACGAATCAAGAGACCTGACTGCCGCCAACTCACT T G PARS2 Ensembl:ENSG00000162396 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs909881902 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11039996 43158 RMVar_ID_43158 Human_SNP_ID_14015997 A-to-I Human chr1 - 54845200 54845200 54845200 CCAGCACTTTGGGAGGCTGAGGCTGGTAGATCACTTGAGGCCAGGAGTTTGAGACCAGCCAAAAC CCAGCACTTTGGGAGGCTGAGGCTGGTAGATCGCTTGAGGCCAGGAGTTTGAGACCAGCCAAAAC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1225005841 Functional Loss SNV dbSNP153 33..33 33 - - - 43159 RMVar_ID_43159 Human_SNP_ID_14016181 A-to-I Human chr1 - 54846123 54846123 54846123 AACAAAAGCGTTTAGGGAAAGTCCAGTATATAACAAACGTGGAGTTACTTTGAGTCAAGCTGGGT AACAAAAGCGTTTAGGGAAAGTCCAGTATATAGCAAACGTGGAGTTACTTTGAGTCAAGCTGGGT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1273994650 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8315040 43160 RMVar_ID_43160 Human_SNP_ID_14017025 A-to-I Human chr1 - 54849713 54849713 54849713 ATGAATCTTCCCTGTCAGGCTCTTACAGCCACAGGCACTGTGTCTACTGTCTGGAAGACATGTCC ATGAATCTTCCCTGTCAGGCTCTTACAGCCACGGGCACTGTGTCTACTGTCTGGAAGACATGTCC T C DHCR24 Ensembl:ENSG00000116133 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1804406 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_358609,Human_RBP_ID_1750760,Human_RBP_ID_3317511,Human_RBP_ID_5108649,Human_RBP_ID_5136290,Human_RBP_ID_5519838,Human_RBP_ID_5842742,Human_RBP_ID_8315047,Human_RBP_ID_9320043,Human_RBP_ID_17219305,Human_RBP_ID_17336499,Human_RBP_ID_17453953,Human_RBP_ID_17647005,Human_RBP_ID_17754610,Human_RBP_ID_18187734,Human_RBP_ID_18232011,Human_RBP_ID_18455145,Human_RBP_ID_21963046,Human_RBP_ID_23205191,Human_RBP_ID_23403571,Human_RBP_ID_26386098,Human_RBP_ID_27185065,Human_RBP_ID_27400042,Human_RBP_ID_27555602,Human_RBP_ID_27596371 Human_miRNA_ID_1994214,Human_miRNA_ID_2226708,Human_miRNA_ID_2502684,Human_miRNA_ID_2584638 RMVar_hsa_circ_78694,RMVar_hsa_circ_133210 43161 RMVar_ID_43161 Human_SNP_ID_14019415 A-to-I Human chr1 - 54859602 54859602 54859602 AAATGAACCAGGTGGGTTGGGGCATGCCTGTAATCCCAGCTACAAGGGAGGCTGAGGCAGGAGAA AAATGAACCAGGTGGGTTGGGGCATGCCTGTAGTCCCAGCTACAAGGGAGGCTGAGGCAGGAGAA T C DHCR24 Ensembl:ENSG00000116133 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1311920439 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 43162 RMVar_ID_43162 Human_SNP_ID_14362598 A-to-I Human chr1 - 56246507 56246507 56246507 TAATCCCAGCACCTTGGGAGGCCAAGGCAGGCAGACCACGAGGTCAAGAGATCGAGACCATCCTG TAATCCCAGCACCTTGGGAGGCCAAGGCAGGCGGACCACGAGGTCAAGAGATCGAGACCATCCTG T C AC119674.1,AC119674.2 Ensembl:ENSG00000260971,Ensembl:ENSG00000284686 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1213172623 Functional Loss SNV dbSNP153 33..33 33 - - - 43163 RMVar_ID_43163 Human_SNP_ID_14401901 A-to-I Human chr1 - 56412987 56412987 56412987 TATATTTAGTAGAGATGGGGTTTGGCTGTGTTAGCCAGTCTGATCTCAAACTCGTGACCTCAGGT TATATTTAGTAGAGATGGGGTTTGGCTGTGTTTGCCAGTCTGATCTCAAACTCGTGACCTCAGGT T A AC119674.1,AC119674.2 Ensembl:ENSG00000260971,Ensembl:ENSG00000284686 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1196528325 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5245738 43164 RMVar_ID_43164 Human_SNP_ID_14460383 A-to-I Human chr1 + 56659827 56659827 56659827 CGACTTGGGGAACTGAGGCGGGAGGATCGCTTAGGCCTGGGAGGTTGAGGCTGCAGTGAGCTGTG CGACTTGGGGAACTGAGGCGGGAGGATCGCTTGGGCCTGGGAGGTTGAGGCTGCAGTGAGCTGTG A G PRKAA2 Ensembl:ENSG00000162409 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1315526226 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_133283 43165 RMVar_ID_43165 Human_SNP_ID_14472631 A-to-I Human chr1 + 56712594 56712594 56712594 GAAAACTAGGCTGGGTGTAGTGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCCAAAGTGGGT GAAAACTAGGCTGGGTGTAGTGGCTCATGCCTCTAATCCCAGCACTTTGGGAGGCCAAAGTGGGT A C PRKAA2 Ensembl:ENSG00000162409 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1434989321 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4060965 43166 RMVar_ID_43166 Human_SNP_ID_14522374 A-to-I Human chr1 + 56911292 56911292 56911292 AGCTAGAAAGTGAGTCACATTTACTTAGTTTTACCATGTGACAGGTCTTTCCCCTATATCATCTC AGCTAGAAAGTGAGTCACATTTACTTAGTTTTGCCATGTGACAGGTCTTTCCCCTATATCATCTC A G C8A Ensembl:ENSG00000157131 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs911096166 Functional Loss SNV dbSNP153 33..33 33 - - - 43167 RMVar_ID_43167 Human_SNP_ID_14577789 A-to-I Human chr1 - 57131809 57131809 57131809 GTTAAGAATCAGCAAATGTACACAAAATGACTAAGGCATAACAGGTAGGAGGTGAGAGTGGCCCA GTTAAGAATCAGCAAATGTACACAAAATGACTGAGGCATAACAGGTAGGAGGTGAGAGTGGCCCA T C DAB1 Ensembl:ENSG00000173406 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1325293100 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16433,RMVar_hsa_circ_302283,RMVar_hsa_circ_331671,RMVar_hsa_circ_350191,RMVar_hsa_circ_133292,RMVar_hsa_circ_50573 43168 RMVar_ID_43168 Human_SNP_ID_14897045 A-to-I Human chr1 - 58481115 58481115 58481115 TGTCCACCACTGTCTAATCCAGACCCTCGATTACTATTCAAACTCAGCACGAAGCATTTTCTTGA TGTCCACCACTGTCTAATCCAGACCCTCGATTGCTATTCAAACTCAGCACGAAGCATTTTCTTGA T C DAB1,OMA1 Ensembl:ENSG00000173406,Ensembl:ENSG00000162600 Protein coding,Protein coding intron,intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1445529350 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_358958,Human_RBP_ID_2156909,Human_RBP_ID_17454037 Human_Splice_Rec_76276,Human_Splice_Rec_76280 43169 RMVar_ID_43169 Human_SNP_ID_14912030 A-to-I Human chr1 - 58541533 58541533 58541533 GGCTCACTGCAGTCTCTTGCCTCCCAGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGCT GGCTCACTGCAGTCTCTTGCCTCCCAGGTTCAGGTGATTCTCCTGCCTCAGCCTCCCAAGTAGCT T C DAB1,OMA1 Ensembl:ENSG00000173406,Ensembl:ENSG00000162600 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1318417033 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5844697,Human_RBP_ID_11216853 Human_Splice_Rec_76310 RMVar_hsa_circ_91862,RMVar_hsa_circ_133313 43170 RMVar_ID_43170 Human_SNP_ID_14912031 A-to-I Human chr1 - 58541540 58541540 58541540 CAATTTTGGCTCACTGCAGTCTCTTGCCTCCCAGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCA CAATTTTGGCTCACTGCAGTCTCTTGCCTCCCGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCA T C DAB1,OMA1 Ensembl:ENSG00000173406,Ensembl:ENSG00000162600 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1222862051 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5844697,Human_RBP_ID_11045389 Human_Splice_Rec_76310 RMVar_hsa_circ_91862,RMVar_hsa_circ_133313 43171 RMVar_ID_43171 Human_SNP_ID_14912834 A-to-I Human chr1 - 58544655 58544655 58544655 CAAGAGGCGAGGTTGCAGTGAGCCGAGGTGGCACCACTGCACTCCAGCCTGGACAACGACAAAGT CAAGAGGCGAGGTTGCAGTGAGCCGAGGTGGCGCCACTGCACTCCAGCCTGGACAACGACAAAGT T C DAB1,OMA1 Ensembl:ENSG00000173406,Ensembl:ENSG00000162600 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1302565728 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91862,RMVar_hsa_circ_133313 43172 RMVar_ID_43172 Human_SNP_ID_14945243 A-to-I Human chr1 - 58679737 58679737 58679737 AGGTGTGAGCCACCACGCCCGGCTGACTCACAATTTTCATCCCCGTGCTTTTGGAGGCTGAGACA AGGTGTGAGCCACCACGCCCGGCTGACTCACAGTTTTCATCCCCGTGCTTTTGGAGGCTGAGACA T C MYSM1 Ensembl:ENSG00000162601 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs757556055 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6020,RMVar_hsa_circ_48132,RMVar_hsa_circ_349454,RMVar_hsa_circ_133331,RMVar_hsa_circ_42328,RMVar_hsa_circ_57002,RMVar_hsa_circ_16034,RMVar_hsa_circ_74276,RMVar_hsa_circ_15785,RMVar_hsa_circ_79900,RMVar_hsa_circ_302066,RMVar_hsa_circ_80620,RMVar_hsa_circ_133333,RMVar_hsa_circ_107393,RMVar_hsa_circ_133334,RMVar_hsa_circ_302714,RMVar_hsa_circ_133336,RMVar_hsa_circ_299644,RMVar_hsa_circ_118224,RMVar_hsa_circ_133337,RMVar_hsa_circ_133338,RMVar_hsa_circ_333497,RMVar_hsa_circ_370707,RMVar_hsa_circ_283856,RMVar_hsa_circ_133341,RMVar_hsa_circ_133342,RMVar_hsa_circ_133340,RMVar_hsa_circ_345053,RMVar_hsa_circ_117668,RMVar_hsa_circ_24115,RMVar_hsa_circ_51754,RMVar_hsa_circ_133343,RMVar_hsa_circ_133346,RMVar_hsa_circ_113655,RMVar_hsa_circ_133345 43173 RMVar_ID_43173 Human_SNP_ID_14970837 A-to-I Human chr1 - 58782017 58782009 58782018 CAACGAAGAAAAAAAATAACACAGAGAGACAGACTTGAGAACTTGACAAGTTGCGACGGAGAGAA CAACGAAGAAAAAAAATAACACAGAGAGACA_________ACTTGACAAGTTGCGACGGAGAGAA TTCTCAAGTC T JUN Ensembl:ENSG00000177606 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs944656711 Functional Loss DEL dbSNP153 32..40 33 - - - Human_RBP_ID_25712,Human_RBP_ID_359156,Human_RBP_ID_1433060,Human_RBP_ID_1751146,Human_RBP_ID_5845411,Human_RBP_ID_11047570,Human_RBP_ID_18410172,Human_RBP_ID_18523322,Human_RBP_ID_27555638,Human_RBP_ID_27800390 Human_miRNA_ID_194633,Human_miRNA_ID_695307,Human_miRNA_ID_700251 43174 RMVar_ID_43174 Human_SNP_ID_386481526 A-to-I Human chr9 - 14694 14694 14694 GACCTGCTTCCCTGGGAGGGGGTGACGGAACCAGCAGTGTGTGGAGACCAGCTTCAAGGAGCGGA GACCTGCTTCCCTGGGAGGGGGTGACGGAACCGGCAGTGTGTGGAGACCAGCTTCAAGGAGCGGA T C WASHC1 Ensembl:ENSG00000181404 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1391864333 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18172953 43175 RMVar_ID_43175 Human_SNP_ID_386523095 A-to-I Human chr9 - 154795 154794 154795 GTTTCTTAACATTTCTCTGTTTGCTATTTTAGACAAGTTGCTTTGGCAGATGCCATTCTCATTAA GTTTCTTAACATTTCTCTGTTTGCTATTTTAG_CAAGTTGCTTTGGCAGATGCCATTCTCATTAA GT G CBWD1 Ensembl:ENSG00000172785 Protein coding CDS GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1256013403 Functional Loss DEL dbSNP153 33..33 33 - - - Human_Splice_Rec_1025894,Human_Splice_Rec_1025895,Human_Splice_Rec_1025922,Human_Splice_Rec_1025923,Human_Splice_Rec_1025948,Human_Splice_Rec_1025949,Human_Splice_Rec_1025978,Human_Splice_Rec_1025979,Human_Splice_Rec_1026102,Human_Splice_Rec_1026103,Human_Splice_Rec_1026124,Human_Splice_Rec_1026125,Human_Splice_Rec_1026154,Human_Splice_Rec_1026155,Human_Splice_Rec_1026194,Human_Splice_Rec_1026195,Human_Splice_Rec_1026220,Human_Splice_Rec_1026221,Human_Splice_Rec_1026238,Human_Splice_Rec_1026239,Human_Splice_Rec_1026250,Human_Splice_Rec_1026251,Human_Splice_Rec_1026278,Human_Splice_Rec_1026279,Human_Splice_Rec_1026284,Human_Splice_Rec_1026285,Human_Splice_Rec_1026296,Human_Splice_Rec_1026297,Human_Splice_Rec_1026312,Human_Splice_Rec_1026322 RMVar_hsa_circ_64156,RMVar_hsa_circ_36154,RMVar_hsa_circ_371776,RMVar_hsa_circ_255219,RMVar_hsa_circ_2994,RMVar_hsa_circ_311748,RMVar_hsa_circ_357198,RMVar_hsa_circ_65925,RMVar_hsa_circ_25594,RMVar_hsa_circ_69511,RMVar_hsa_circ_320223,RMVar_hsa_circ_73448 43176 RMVar_ID_43176 Human_SNP_ID_386523096 A-to-I Human chr9 - 154795 154795 154795 GTTTCTTAACATTTCTCTGTTTGCTATTTTAGACAAGTTGCTTTGGCAGATGCCATTCTCATTAA GTTTCTTAACATTTCTCTGTTTGCTATTTTAGTCAAGTTGCTTTGGCAGATGCCATTCTCATTAA T A CBWD1 Ensembl:ENSG00000172785 Protein coding CDS GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs2785333 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1025894,Human_Splice_Rec_1025895,Human_Splice_Rec_1025922,Human_Splice_Rec_1025923,Human_Splice_Rec_1025948,Human_Splice_Rec_1025949,Human_Splice_Rec_1025978,Human_Splice_Rec_1025979,Human_Splice_Rec_1026102,Human_Splice_Rec_1026103,Human_Splice_Rec_1026124,Human_Splice_Rec_1026125,Human_Splice_Rec_1026154,Human_Splice_Rec_1026155,Human_Splice_Rec_1026194,Human_Splice_Rec_1026195,Human_Splice_Rec_1026220,Human_Splice_Rec_1026221,Human_Splice_Rec_1026238,Human_Splice_Rec_1026239,Human_Splice_Rec_1026250,Human_Splice_Rec_1026251,Human_Splice_Rec_1026278,Human_Splice_Rec_1026279,Human_Splice_Rec_1026284,Human_Splice_Rec_1026285,Human_Splice_Rec_1026296,Human_Splice_Rec_1026297,Human_Splice_Rec_1026312,Human_Splice_Rec_1026322 RMVar_hsa_circ_64156,RMVar_hsa_circ_36154,RMVar_hsa_circ_371776,RMVar_hsa_circ_255219,RMVar_hsa_circ_2994,RMVar_hsa_circ_311748,RMVar_hsa_circ_357198,RMVar_hsa_circ_65925,RMVar_hsa_circ_25594,RMVar_hsa_circ_69511,RMVar_hsa_circ_320223,RMVar_hsa_circ_73448 43177 RMVar_ID_43177 Human_SNP_ID_386523097 A-to-I Human chr9 - 154795 154795 154795 GTTTCTTAACATTTCTCTGTTTGCTATTTTAGACAAGTTGCTTTGGCAGATGCCATTCTCATTAA GTTTCTTAACATTTCTCTGTTTGCTATTTTAGGCAAGTTGCTTTGGCAGATGCCATTCTCATTAA T C CBWD1 Ensembl:ENSG00000172785 Protein coding CDS GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs2785333 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_Splice_Rec_1025894,Human_Splice_Rec_1025895,Human_Splice_Rec_1025922,Human_Splice_Rec_1025923,Human_Splice_Rec_1025948,Human_Splice_Rec_1025949,Human_Splice_Rec_1025978,Human_Splice_Rec_1025979,Human_Splice_Rec_1026102,Human_Splice_Rec_1026103,Human_Splice_Rec_1026124,Human_Splice_Rec_1026125,Human_Splice_Rec_1026154,Human_Splice_Rec_1026155,Human_Splice_Rec_1026194,Human_Splice_Rec_1026195,Human_Splice_Rec_1026220,Human_Splice_Rec_1026221,Human_Splice_Rec_1026238,Human_Splice_Rec_1026239,Human_Splice_Rec_1026250,Human_Splice_Rec_1026251,Human_Splice_Rec_1026278,Human_Splice_Rec_1026279,Human_Splice_Rec_1026284,Human_Splice_Rec_1026285,Human_Splice_Rec_1026296,Human_Splice_Rec_1026297,Human_Splice_Rec_1026312,Human_Splice_Rec_1026322 RMVar_hsa_circ_64156,RMVar_hsa_circ_36154,RMVar_hsa_circ_371776,RMVar_hsa_circ_255219,RMVar_hsa_circ_2994,RMVar_hsa_circ_311748,RMVar_hsa_circ_357198,RMVar_hsa_circ_65925,RMVar_hsa_circ_25594,RMVar_hsa_circ_69511,RMVar_hsa_circ_320223,RMVar_hsa_circ_73448 43178 RMVar_ID_43178 Human_SNP_ID_386578316 A-to-I Human chr9 + 323495 323495 323495 CGCTTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGCGCCTGGCCAAAATCT CGCTTGCCTCGGCCTCCCAAAGTGCTGGGATTCCAGGCATGAGCCACTGCGCCTGGCCAAAATCT A C DOCK8 Ensembl:ENSG00000107099 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1425908729 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84888,RMVar_hsa_circ_255222,RMVar_hsa_circ_58407,RMVar_hsa_circ_49713,RMVar_hsa_circ_58623,RMVar_hsa_circ_53552,RMVar_hsa_circ_62831,RMVar_hsa_circ_71072,RMVar_hsa_circ_20187,RMVar_hsa_circ_348468 43179 RMVar_ID_43179 Human_SNP_ID_386578317 A-to-I Human chr9 + 323495 323495 323495 CGCTTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGCGCCTGGCCAAAATCT CGCTTGCCTCGGCCTCCCAAAGTGCTGGGATTGCAGGCATGAGCCACTGCGCCTGGCCAAAATCT A G DOCK8 Ensembl:ENSG00000107099 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1425908729 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84888,RMVar_hsa_circ_255222,RMVar_hsa_circ_58407,RMVar_hsa_circ_49713,RMVar_hsa_circ_58623,RMVar_hsa_circ_53552,RMVar_hsa_circ_62831,RMVar_hsa_circ_71072,RMVar_hsa_circ_20187,RMVar_hsa_circ_348468 43180 RMVar_ID_43180 Human_SNP_ID_386599769 A-to-I Human chr9 + 388659 388659 388659 TCACTGCAACCTCTGCCTCCCAGGTTTAAGTGATTCTCCTGCCTCAGCCTCCAGAGTAGCTGGGA TCACTGCAACCTCTGCCTCCCAGGTTTAAGTGGTTCTCCTGCCTCAGCCTCCAGAGTAGCTGGGA A G DOCK8 Ensembl:ENSG00000107099 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs749445250 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11382,RMVar_hsa_circ_267089,RMVar_hsa_circ_36126,RMVar_hsa_circ_75286,RMVar_hsa_circ_367189,RMVar_hsa_circ_35934,RMVar_hsa_circ_72376 43181 RMVar_ID_43181 Human_SNP_ID_386616729 A-to-I Human chr9 + 431126 431126 431126 GAACACCTGAGCTCAAGTGATCTTCCCTCCTCAGCCCCCCAAAGTACTGAGATTATAGGCATGAG GAACACCTGAGCTCAAGTGATCTTCCCTCCTCGGCCCCCCAAAGTACTGAGATTATAGGCATGAG A G DOCK8 Ensembl:ENSG00000107099 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1362297196 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265717,RMVar_hsa_circ_266071 43182 RMVar_ID_43182 Human_SNP_ID_386640583 A-to-I Human chr9 + 507199 507199 507199 ACATAGCGAGACTCCGTCTCTACAAAAAAAATAAAAAATAACCGGATATGGTGGCACATGCACCT ACATAGCGAGACTCCGTCTCTACAAAAAAAATGAAAAATAACCGGATATGGTGGCACATGCACCT A G KANK1 Ensembl:ENSG00000107104 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1012274931 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7929786,Human_RBP_ID_16685248 RMVar_hsa_circ_255233,RMVar_hsa_circ_105660,RMVar_hsa_circ_78220,RMVar_hsa_circ_255234 43183 RMVar_ID_43183 Human_SNP_ID_386640595 A-to-I Human chr9 + 507244 507244 507244 ATATGGTGGCACATGCACCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGGATTGCTTTAG ATATGGTGGCACATGCACCTGTAGTCCCAGCTGCTTGGGAGGCTGAGGCAGGAGGATTGCTTTAG A G KANK1 Ensembl:ENSG00000107104 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1245960913 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16685250 RMVar_hsa_circ_255233,RMVar_hsa_circ_105660,RMVar_hsa_circ_78220,RMVar_hsa_circ_255234 43184 RMVar_ID_43184 Human_SNP_ID_386640675 A-to-I Human chr9 + 507483 507483 507483 ACAGTATCAGCTCACTGCAACCTCCGCCTCCCAGGTTTAAGCGATTCTCCTGCCTCAGCCTCCCA ACAGTATCAGCTCACTGCAACCTCCGCCTCCCGGGTTTAAGCGATTCTCCTGCCTCAGCCTCCCA A G KANK1 Ensembl:ENSG00000107104 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1173502657 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_255233,RMVar_hsa_circ_105660,RMVar_hsa_circ_78220,RMVar_hsa_circ_255234 43185 RMVar_ID_43185 Human_SNP_ID_386641665 A-to-I Human chr9 + 509896 509896 509896 AGAGCTCGCTGTAACCGTGAACTGCTGGGCCCAAGCAATCCTCCCGCCTCAGCCTGCCTCCCGAG AGAGCTCGCTGTAACCGTGAACTGCTGGGCCCGAGCAATCCTCCCGCCTCAGCCTGCCTCCCGAG A G KANK1 Ensembl:ENSG00000107104 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027881753 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_255233,RMVar_hsa_circ_105660,RMVar_hsa_circ_78220,RMVar_hsa_circ_255234 43186 RMVar_ID_43186 Human_SNP_ID_386649699 A-to-I Human chr9 + 531350 531350 531350 CTACTGAGGAGACTGAGGTGCGAGGGTTGCTTAAACCCAGGAGGTGGAGGCTGCAGTGAGCTGTA CTACTGAGGAGACTGAGGTGCGAGGGTTGCTTTAACCCAGGAGGTGGAGGCTGCAGTGAGCTGTA A T KANK1 Ensembl:ENSG00000107104 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs897505796 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_255233,RMVar_hsa_circ_105660,RMVar_hsa_circ_78220,RMVar_hsa_circ_255234 43187 RMVar_ID_43187 Human_SNP_ID_386683349 A-to-I Human chr9 + 623447 623446 623447 CCCTGTCTCTACAAGAAATACAAAAATTAGCTAGGCGTGGTGGCATGCACCTATAGTCTCAGTTA CCCTGTCTCTACAAGAAATACAAAAATTAGCT_GGCGTGGTGGCATGCACCTATAGTCTCAGTTA TA T KANK1 Ensembl:ENSG00000107104 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348003714 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_255233,RMVar_hsa_circ_105660,RMVar_hsa_circ_78220,RMVar_hsa_circ_255234,RMVar_hsa_circ_255235,RMVar_hsa_circ_123041 43188 RMVar_ID_43188 Human_SNP_ID_386691493 A-to-I Human chr9 + 645296 645296 645296 AACCCCGTCTATACAAAACTACAAAAATTAGCAAGCCATGGTGGTGGACATCTGTAATCCCAGCT AACCCCGTCTATACAAAACTACAAAAATTAGCCAGCCATGGTGGTGGACATCTGTAATCCCAGCT A C KANK1 Ensembl:ENSG00000107104 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1294149216 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_255233,RMVar_hsa_circ_105660,RMVar_hsa_circ_78220,RMVar_hsa_circ_255234,RMVar_hsa_circ_255235,RMVar_hsa_circ_123041 43189 RMVar_ID_43189 Human_SNP_ID_386698773 A-to-I Human chr9 + 665506 665506 665506 GCAAATGGCATGGATTTATATCTGGGTTCACTATTCTGTTCAGTCGGTGTTTGTGTCTGTTTTTT GCAAATGGCATGGATTTATATCTGGGTTCACTCTTCTGTTCAGTCGGTGTTTGTGTCTGTTTTTT A C KANK1 Ensembl:ENSG00000107104 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1011640490 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_255233,RMVar_hsa_circ_105660,RMVar_hsa_circ_78220,RMVar_hsa_circ_255234,RMVar_hsa_circ_255235,RMVar_hsa_circ_123041 43190 RMVar_ID_43190 Human_SNP_ID_386698774 A-to-I Human chr9 + 665506 665506 665506 GCAAATGGCATGGATTTATATCTGGGTTCACTATTCTGTTCAGTCGGTGTTTGTGTCTGTTTTTT GCAAATGGCATGGATTTATATCTGGGTTCACTGTTCTGTTCAGTCGGTGTTTGTGTCTGTTTTTT A G KANK1 Ensembl:ENSG00000107104 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1011640490 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_255233,RMVar_hsa_circ_105660,RMVar_hsa_circ_78220,RMVar_hsa_circ_255234,RMVar_hsa_circ_255235,RMVar_hsa_circ_123041 43191 RMVar_ID_43191 Human_SNP_ID_386724281 A-to-I Human chr9 + 736530 736530 736530 TTCAGTTTGAGACCAGCCTGGGCAACATGGCAAAACCCTGTCTCTACAAAAATTAGCCAGGTATG TTCAGTTTGAGACCAGCCTGGGCAACATGGCACAACCCTGTCTCTACAAAAATTAGCCAGGTATG A C KANK1 Ensembl:ENSG00000107104 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1197495578 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17579169 RMVar_hsa_circ_1292,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_51141,RMVar_hsa_circ_358760,RMVar_hsa_circ_255239,RMVar_hsa_circ_303987,RMVar_hsa_circ_255240,RMVar_hsa_circ_255241 43192 RMVar_ID_43192 Human_SNP_ID_387216610 A-to-I Human chr9 + 2129303 2129303 2129303 AGCCGGGCGTGGTGGCACGTGCCTGTAGTCCCAGCTGCTTGGGAGGCTGAGGCAGGGGAATCGCT AGCCGGGCGTGGTGGCACGTGCCTGTAGTCCCGGCTGCTTGGGAGGCTGAGGCAGGGGAATCGCT A G SMARCA2 Ensembl:ENSG00000080503 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1362084939 Functional Loss SNV dbSNP153 33..33 33 - - - 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 43193 RMVar_ID_43193 Human_SNP_ID_387222746 A-to-I Human chr9 + 2148709 2148709 2148709 TTTTTTATTTTTTGTAGAGACAGAGTTTTGCCATGTTGCCTAGGCTGGTCTCTAACTCATGGCCT TTTTTTATTTTTTGTAGAGACAGAGTTTTGCCGTGTTGCCTAGGCTGGTCTCTAACTCATGGCCT A G SMARCA2 Ensembl:ENSG00000080503 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs921800689 Functional Loss SNV dbSNP153 33..33 33 - - - 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_255273,RMVar_hsa_circ_255272 43194 RMVar_ID_43194 Human_SNP_ID_387408135 A-to-I Human chr9 - 2715012 2715012 2715012 AGCCGGGCTGGGCATGTTGGCGGGTGCCTGTAATCCCAGTTACTCAGGAGGCTGACACACAAGAA AGCCGGGCTGGGCATGTTGGCGGGTGCCTGTAGTCCCAGTTACTCAGGAGGCTGACACACAAGAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs771013421 Functional Loss SNV dbSNP153 33..33 33 - - - 43195 RMVar_ID_43195 Human_SNP_ID_387421108 A-to-I Human chr9 - 2752215 2752215 2752215 TGGCAATTGTATTAGTCCGTTTTCACACTGCTATATAGAACTAACTGAGCCTGGGTAATTTATTA TGGCAATTGTATTAGTCCGTTTTCACACTGCTGTATAGAACTAACTGAGCCTGGGTAATTTATTA T C PUM3 Ensembl:ENSG00000080608 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1015114769 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7919304,Human_RBP_ID_16648608 43196 RMVar_ID_43196 Human_SNP_ID_387421109 A-to-I Human chr9 - 2752215 2752215 2752215 TGGCAATTGTATTAGTCCGTTTTCACACTGCTATATAGAACTAACTGAGCCTGGGTAATTTATTA TGGCAATTGTATTAGTCCGTTTTCACACTGCTCTATAGAACTAACTGAGCCTGGGTAATTTATTA T G PUM3 Ensembl:ENSG00000080608 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1015114769 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7919304,Human_RBP_ID_16648608 43197 RMVar_ID_43197 Human_SNP_ID_387424114 A-to-I Human chr9 - 2762062 2762062 2762062 CTGAAGGCTCCTGTCTATAACTAACGTTAAATAAATTTGTGTGCCTTTTCTCCTATTAATCTGCC CTGAAGGCTCCTGTCTATAACTAACGTTAAATGAATTTGTGTGCCTTTTCTCCTATTAATCTGCC T C PUM3 Ensembl:ENSG00000080608 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1342295200 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26737996 43198 RMVar_ID_43198 Human_SNP_ID_387424116 A-to-I Human chr9 - 2762066 2762066 2762066 CATTCTGAAGGCTCCTGTCTATAACTAACGTTAAATAAATTTGTGTGCCTTTTCTCCTATTAATC CATTCTGAAGGCTCCTGTCTATAACTAACGTTTAATAAATTTGTGTGCCTTTTCTCCTATTAATC T A PUM3 Ensembl:ENSG00000080608 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs930440604 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26737996 43199 RMVar_ID_43199 Human_SNP_ID_387424134 A-to-I Human chr9 - 2762109 2762109 2762109 AACGGTAAATGAGCTTCTGCACCACATAGGGAAGCTGGGTCTTCATTCTGAAGGCTCCTGTCTAT AACGGTAAATGAGCTTCTGCACCACATAGGGAGGCTGGGTCTTCATTCTGAAGGCTCCTGTCTAT T C PUM3 Ensembl:ENSG00000080608 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1021590710 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21716646 43200 RMVar_ID_43200 Human_SNP_ID_387425355 A-to-I Human chr9 - 2766033 2766033 2766033 GTATTGTGGGGGCCATAGGCTCTTGGCCTCCTAAAGGCTCGCTGAAAATCACTGACATAAAGCGG GTATTGTGGGGGCCATAGGCTCTTGGCCTCCTGAAGGCTCGCTGAAAATCACTGACATAAAGCGG T C PUM3 Ensembl:ENSG00000080608 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1278820948 Functional Loss SNV dbSNP153 33..33 33 - - - 43201 RMVar_ID_43201 Human_SNP_ID_387425455 A-to-I Human chr9 - 2766315 2766315 2766315 TTGGCCAGGCTGGTCTCGAACTCCTGACCTTAAGTGATACGCCTGCCTCGGTCTCCTAAAATGCT TTGGCCAGGCTGGTCTCGAACTCCTGACCTTAGGTGATACGCCTGCCTCGGTCTCCTAAAATGCT T C PUM3 Ensembl:ENSG00000080608 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1214834446 Functional Loss SNV dbSNP153 33..33 33 - - - 43202 RMVar_ID_43202 Human_SNP_ID_387425456 A-to-I Human chr9 - 2766316 2766316 2766316 ATTGGCCAGGCTGGTCTCGAACTCCTGACCTTAAGTGATACGCCTGCCTCGGTCTCCTAAAATGC ATTGGCCAGGCTGGTCTCGAACTCCTGACCTTGAGTGATACGCCTGCCTCGGTCTCCTAAAATGC T C PUM3 Ensembl:ENSG00000080608 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1009691224 Functional Loss SNV dbSNP153 33..33 33 - - - 43203 RMVar_ID_43203 Human_SNP_ID_387425472 A-to-I Human chr9 - 2766384 2766384 2766384 GGATTATGGGCATGCGCCACCACGCCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGTTTTCAC GGATTATGGGCATGCGCCACCACGCCTGGCTAGTTTTTGTATTTTTAGTAGAGACAGGTTTTCAC T C PUM3 Ensembl:ENSG00000080608 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs902927817 Functional Loss SNV dbSNP153 33..33 33 - - - 43204 RMVar_ID_43204 Human_SNP_ID_387426941 A-to-I Human chr9 - 2770849 2770848 2770849 CTGATCACGAGAATGGCTTGAACCCCAGAGGCAGAGGTTGCAGTGAGCCAAGATCATGCCACTGC CTGATCACGAGAATGGCTTGAACCCCAGAGGC_GAGGTTGCAGTGAGCCAAGATCATGCCACTGC CT C PUM3 Ensembl:ENSG00000080608 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1214991849 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_16649256 43205 RMVar_ID_43205 Human_SNP_ID_387426942 A-to-I Human chr9 - 2770849 2770849 2770849 CTGATCACGAGAATGGCTTGAACCCCAGAGGCAGAGGTTGCAGTGAGCCAAGATCATGCCACTGC CTGATCACGAGAATGGCTTGAACCCCAGAGGCGGAGGTTGCAGTGAGCCAAGATCATGCCACTGC T C PUM3 Ensembl:ENSG00000080608 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs551379583 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16649256 43206 RMVar_ID_43206 Human_SNP_ID_387429164 A-to-I Human chr9 - 2777773 2777773 2777773 GGCCAGAATGGTCTTGAACTTCTGACTTCATGATCCGCACGCCTTGGCCTCCCAAGGTGCTGGGA GGCCAGAATGGTCTTGAACTTCTGACTTCATGGTCCGCACGCCTTGGCCTCCCAAGGTGCTGGGA T C PUM3 Ensembl:ENSG00000080608 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904714970 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16649434 43207 RMVar_ID_43207 Human_SNP_ID_387429220 A-to-I Human chr9 - 2777951 2777951 2777951 CACTGTCGCCTGGCCTAGAGTGCAGTCGTGCAATCTTGGCTCACCGCAACCTCCACCTCCCTGGT CACTGTCGCCTGGCCTAGAGTGCAGTCGTGCAGTCTTGGCTCACCGCAACCTCCACCTCCCTGGT T C PUM3 Ensembl:ENSG00000080608 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs748199080 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_255305,RMVar_hsa_circ_255304 43208 RMVar_ID_43208 Human_SNP_ID_387436170 A-to-I Human chr9 - 2797785 2797785 2797785 GGAAGGCCGAGGTTGCAGTGAGCTGAGATCGCACCCCTGCACTCCATCCTGGGTGACAGAACAAG GGAAGGCCGAGGTTGCAGTGAGCTGAGATCGCGCCCCTGCACTCCATCCTGGGTGACAGAACAAG T C PUM3 Ensembl:ENSG00000080608 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1268451878 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7919834 RMVar_hsa_circ_255306 43209 RMVar_ID_43209 Human_SNP_ID_387436209 A-to-I Human chr9 - 2797923 2797923 2797923 GGCAGGAGTTCAAAACCAATCTGGCCAACACAATGAAACCTCATCTCTACCAAAAATACAAAAAT GGCAGGAGTTCAAAACCAATCTGGCCAACACAGTGAAACCTCATCTCTACCAAAAATACAAAAAT T C PUM3 Ensembl:ENSG00000080608 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1038620757 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_255306 43210 RMVar_ID_43210 Human_SNP_ID_387436230 A-to-I Human chr9 - 2797992 2797992 2797992 TCGTAAGTAGGCTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGCGGATCACT TCGTAAGTAGGCTGGCTCACACCTGTAATCCCGGCACTTTGGGAGGCCGAGGTGGGCGGATCACT T C PUM3 Ensembl:ENSG00000080608 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs545315240 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_255306 43211 RMVar_ID_43211 Human_SNP_ID_387436231 A-to-I Human chr9 - 2797992 2797992 2797992 TCGTAAGTAGGCTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGCGGATCACT TCGTAAGTAGGCTGGCTCACACCTGTAATCCCCGCACTTTGGGAGGCCGAGGTGGGCGGATCACT T G PUM3 Ensembl:ENSG00000080608 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs545315240 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_255306 43212 RMVar_ID_43212 Human_SNP_ID_387436374 A-to-I Human chr9 - 2798457 2798455 2798457 ATCTACCAGTAAGCACATACTGACTTAATGTTATCACATTCAGCAGTAGGCAGTGATAGAGAAAC ATCTACCAGTAAGCACATACTGACTTAATGTT__CACATTCAGCAGTAGGCAGTGATAGAGAAAC GAT G PUM3 Ensembl:ENSG00000080608 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1298114402 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_8702767 RMVar_hsa_circ_255306 43213 RMVar_ID_43213 Human_SNP_ID_387436375 A-to-I Human chr9 - 2798457 2798457 2798457 ATCTACCAGTAAGCACATACTGACTTAATGTTATCACATTCAGCAGTAGGCAGTGATAGAGAAAC ATCTACCAGTAAGCACATACTGACTTAATGTTGTCACATTCAGCAGTAGGCAGTGATAGAGAAAC T C PUM3 Ensembl:ENSG00000080608 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1160421528 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8702767 RMVar_hsa_circ_255306 43214 RMVar_ID_43214 Human_SNP_ID_387436600 A-to-I Human chr9 - 2799117 2799117 2799117 GTCTCGATCTGACCTCGTGATCCCCCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGCCGTGAG GTCTCGATCTGACCTCGTGATCCCCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGCCGTGAG T C PUM3 Ensembl:ENSG00000080608 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1267731433 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_255306 43215 RMVar_ID_43215 Human_SNP_ID_387436662 A-to-I Human chr9 - 2799227 2799227 2799227 CTCCTGCCTCCGCCTCCTGAGTAGCTGGGACTACAGGCGCCCACCACCACGCCTGGCTAATCTTT CTCCTGCCTCCGCCTCCTGAGTAGCTGGGACTGCAGGCGCCCACCACCACGCCTGGCTAATCTTT T C PUM3 Ensembl:ENSG00000080608 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs904497654 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_255306 43216 RMVar_ID_43216 Human_SNP_ID_387450348 A-to-I Human chr9 - 2841421 2841421 2841421 TGGGATTACATGTTTGCAACACCACCATGCCCAGCTAAATTTTGTATTTTTAGTAGAGATGGGGT TGGGATTACATGTTTGCAACACCACCATGCCCGGCTAAATTTTGTATTTTTAGTAGAGATGGGGT T C PUM3 Ensembl:ENSG00000080608 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1422457238 Functional Loss SNV dbSNP153 33..33 33 - - - 43217 RMVar_ID_43217 Human_SNP_ID_387637800 A-to-I Human chr9 - 3423903 3423903 3423903 GACCTTGTGGTCCCCCCGCCTCGGCCTCCCAGAGTGCTGGGATTACAGGCGTGAGCCACCGCGCC GACCTTGTGGTCCCCCCGCCTCGGCCTCCCAGCGTGCTGGGATTACAGGCGTGAGCCACCGCGCC T G RFX3 Ensembl:ENSG00000080298 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1272905229 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26169,RMVar_hsa_circ_255365,RMVar_hsa_circ_97404,RMVar_hsa_circ_255356,RMVar_hsa_circ_24362,RMVar_hsa_circ_122845,RMVar_hsa_circ_127387,RMVar_hsa_circ_255366,RMVar_hsa_circ_311583,RMVar_hsa_circ_255376 43218 RMVar_ID_43218 Human_SNP_ID_387645266 A-to-I Human chr9 - 3448578 3448578 3448578 GGAAGGAGTTTGAGGCTGCAATTCACGCTATGATGGCGCCACCGCAGTCTAGCCTGGGCGACAGA GGAAGGAGTTTGAGGCTGCAATTCACGCTATGGTGGCGCCACCGCAGTCTAGCCTGGGCGACAGA T C RFX3 Ensembl:ENSG00000080298 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1014790892 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26169,RMVar_hsa_circ_255365,RMVar_hsa_circ_97404,RMVar_hsa_circ_255356,RMVar_hsa_circ_24362,RMVar_hsa_circ_122845,RMVar_hsa_circ_127387,RMVar_hsa_circ_255366,RMVar_hsa_circ_311583,RMVar_hsa_circ_255376 43219 RMVar_ID_43219 Human_SNP_ID_387656842 A-to-I Human chr9 - 3487102 3487102 3487102 CCTGTAATCTCAGCACTTTGGGATGTCAAGGTAGAAGGATCCCTTGAGCCCAGGAATTGGAGACC CCTGTAATCTCAGCACTTTGGGATGTCAAGGTGGAAGGATCCCTTGAGCCCAGGAATTGGAGACC T C RFX3 Ensembl:ENSG00000080298 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs367903646 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26169,RMVar_hsa_circ_255365,RMVar_hsa_circ_97404,RMVar_hsa_circ_255356,RMVar_hsa_circ_24362,RMVar_hsa_circ_122845,RMVar_hsa_circ_127387,RMVar_hsa_circ_255366,RMVar_hsa_circ_311583,RMVar_hsa_circ_255376,RMVar_hsa_circ_255377 43220 RMVar_ID_43220 Human_SNP_ID_387662055 A-to-I Human chr9 - 3504166 3504150 3504166 ATATAATATATAATATGTATAATATATAATATATATAATATATAATATGTATAATATATAATATA ATATAATATATAATATGTATAATATATAATAT________________GTATAATATATAATATA CATATTATATATTATAT C RFX3 Ensembl:ENSG00000080298 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1180235722 Functional Loss DEL dbSNP153 33..48 33 - - - 43221 RMVar_ID_43221 Human_SNP_ID_387662074 A-to-I Human chr9 - 3504170 3504163 3504170 ATATATATAATATATAATATGTATAATATATAATATATATAATATATAATATGTATAATATATAA ATATATATAATATATAATATGTATAATATATA_______TAATATATAATATGTATAATATATAA ATATATAT A RFX3 Ensembl:ENSG00000080298 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1296789613 Functional Loss DEL dbSNP153 33..39 33 - - - 43222 RMVar_ID_43222 Human_SNP_ID_387662078 A-to-I Human chr9 - 3504166 3504166 3504166 ATATAATATATAATATGTATAATATATAATATATATAATATATAATATGTATAATATATAATATA ATATAATATATAATATGTATAATATATAATATTTATAATATATAATATGTATAATATATAATATA T A RFX3 Ensembl:ENSG00000080298 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs550232391 Functional Loss SNV dbSNP153 33..33 33 - - - 43223 RMVar_ID_43223 Human_SNP_ID_387662079 A-to-I Human chr9 - 3504166 3504166 3504166 ATATAATATATAATATGTATAATATATAATATATATAATATATAATATGTATAATATATAATATA ATATAATATATAATATGTATAATATATAATATGTATAATATATAATATGTATAATATATAATATA T C RFX3 Ensembl:ENSG00000080298 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs550232391 Functional Loss SNV dbSNP153 33..33 33 - - - 43224 RMVar_ID_43224 Human_SNP_ID_387662082 A-to-I Human chr9 - 3504170 3504170 3504170 ATATATATAATATATAATATGTATAATATATAATATATATAATATATAATATGTATAATATATAA ATATATATAATATATAATATGTATAATATATACTATATATAATATATAATATGTATAATATATAA T G RFX3 Ensembl:ENSG00000080298 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs867306109 Functional Loss SNV dbSNP153 33..33 33 - - - 43225 RMVar_ID_43225 Human_SNP_ID_387662106 A-to-I Human chr9 - 3504202 3504182 3504202 TATAGTATATAATATAGTATATAATATATATAATATATATAATATATAATATGTATAATATATAA TATAGTATATAATATAGTATATAATATATATA____________________GTATAATATATAA CATATTATATATTATATATAT C RFX3 Ensembl:ENSG00000080298 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1564183283 Functional Loss DEL dbSNP153 33..52 33 - - - 43226 RMVar_ID_43226 Human_SNP_ID_387662140 A-to-I Human chr9 - 3504200 3504200 3504200 TAGTATATAATATAGTATATAATATATATAATATATATAATATATAATATGTATAATATATAATA TAGTATATAATATAGTATATAATATATATAATGTATATAATATATAATATGTATAATATATAATA T C RFX3 Ensembl:ENSG00000080298 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1006298503 Functional Loss SNV dbSNP153 33..33 33 - - - 43227 RMVar_ID_43227 Human_SNP_ID_387662142 A-to-I Human chr9 - 3504202 3504201 3504203 TATAGTATATAATATAGTATATAATATATATAATATATATAATATATAATATGTATAATATATAA TATAGTATATAATATAGTATATAATATATAT__TATATATAATATATAATATGTATAATATATAA ATT A RFX3 Ensembl:ENSG00000080298 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1482257719 Functional Loss DEL dbSNP153 32..33 33 - - - 43228 RMVar_ID_43228 Human_SNP_ID_387662147 A-to-I Human chr9 - 3504202 3504202 3504202 TATAGTATATAATATAGTATATAATATATATAATATATATAATATATAATATGTATAATATATAA TATAGTATATAATATAGTATATAATATATATATTATATATAATATATAATATGTATAATATATAA T A RFX3 Ensembl:ENSG00000080298 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1200946702 Functional Loss SNV dbSNP153 33..33 33 - - - 43229 RMVar_ID_43229 Human_SNP_ID_387662148 A-to-I Human chr9 - 3504202 3504202 3504202 TATAGTATATAATATAGTATATAATATATATAATATATATAATATATAATATGTATAATATATAA TATAGTATATAATATAGTATATAATATATATAGTATATATAATATATAATATGTATAATATATAA T C RFX3 Ensembl:ENSG00000080298 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1200946702 Functional Loss SNV dbSNP153 33..33 33 - - - 43230 RMVar_ID_43230 Human_SNP_ID_387662155 A-to-I Human chr9 - 3504211 3504208 3504211 TATATAATATATAGTATATAATATAGTATATAATATATATAATATATATAATATATAATATGTAT TATATAATATATAGTATATAATATAGTATATA___TATATAATATATATAATATATAATATGTAT ATAT A RFX3 Ensembl:ENSG00000080298 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1400735037 Functional Loss DEL dbSNP153 33..35 33 - - - 43231 RMVar_ID_43231 Human_SNP_ID_387662157 A-to-I Human chr9 - 3504212 3504209 3504213 ATATATAATATATAGTATATAATATAGTATATAATATATATAATATATATAATATATAATATGTA ATATATAATATATAGTATATAATATAGTATA____ATATATAATATATATAATATATAATATGTA TATTA T RFX3 Ensembl:ENSG00000080298 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1406068085 Functional Loss DEL dbSNP153 32..35 33 - - - 43232 RMVar_ID_43232 Human_SNP_ID_387662159 A-to-I Human chr9 - 3504211 3504211 3504211 TATATAATATATAGTATATAATATAGTATATAATATATATAATATATATAATATATAATATGTAT TATATAATATATAGTATATAATATAGTATATATTATATATAATATATATAATATATAATATGTAT T A RFX3 Ensembl:ENSG00000080298 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1157374928 Functional Loss SNV dbSNP153 33..33 33 - - - 43233 RMVar_ID_43233 Human_SNP_ID_387662160 A-to-I Human chr9 - 3504212 3504212 3504212 ATATATAATATATAGTATATAATATAGTATATAATATATATAATATATATAATATATAATATGTA ATATATAATATATAGTATATAATATAGTATATGATATATATAATATATATAATATATAATATGTA T C RFX3 Ensembl:ENSG00000080298 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1462732556 Functional Loss SNV dbSNP153 33..33 33 - - - 43234 RMVar_ID_43234 Human_SNP_ID_387662250 A-to-I Human chr9 - 3504320 3504281 3504320 ATGCTATGTGGCATATAATATATATTTTATATATAATATATGCTATGTGGTATATAATATATATT ATGCTATGTGGCATATAATATATATTTTATAT_________________________________ CATATAAAATATATATTATATACCACATAGCATATATTAT C RFX3 Ensembl:ENSG00000080298 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1564183706 Functional Loss DEL dbSNP153 33..65 33 - - - 43235 RMVar_ID_43235 Human_SNP_ID_387662286 A-to-I Human chr9 - 3504318 3504315 3504319 GCTATGTGGCATATAATATATATTTTATATATAATATATGCTATGTGGTATATAATATATATTTT GCTATGTGGCATATAATATATATTTTATATA____ATATGCTATGTGGTATATAATATATATTTT TATTA T RFX3 Ensembl:ENSG00000080298 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1406038284 Functional Loss DEL dbSNP153 32..35 33 - - - 43236 RMVar_ID_43236 Human_SNP_ID_387662288 A-to-I Human chr9 - 3504317 3504317 3504317 CTATGTGGCATATAATATATATTTTATATATAATATATGCTATGTGGTATATAATATATATTTTA CTATGTGGCATATAATATATATTTTATATATAGTATATGCTATGTGGTATATAATATATATTTTA T C RFX3 Ensembl:ENSG00000080298 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1413234909 Functional Loss SNV dbSNP153 33..33 33 - - - 43237 RMVar_ID_43237 Human_SNP_ID_387662290 A-to-I Human chr9 - 3504320 3504317 3504321 ATGCTATGTGGCATATAATATATATTTTATATATAATATATGCTATGTGGTATATAATATATATT ATGCTATGTGGCATATAATATATATTTTATA____ATATATGCTATGTGGTATATAATATATATT TTATA T RFX3 Ensembl:ENSG00000080298 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1564183791 Functional Loss DEL dbSNP153 32..35 33 - - - 43238 RMVar_ID_43238 Human_SNP_ID_387662291 A-to-I Human chr9 - 3504318 3504318 3504318 GCTATGTGGCATATAATATATATTTTATATATAATATATGCTATGTGGTATATAATATATATTTT GCTATGTGGCATATAATATATATTTTATATATGATATATGCTATGTGGTATATAATATATATTTT T C RFX3 Ensembl:ENSG00000080298 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1161737869 Functional Loss SNV dbSNP153 33..33 33 - - - 43239 RMVar_ID_43239 Human_SNP_ID_387662298 A-to-I Human chr9 - 3504320 3504320 3504320 ATGCTATGTGGCATATAATATATATTTTATATATAATATATGCTATGTGGTATATAATATATATT ATGCTATGTGGCATATAATATATATTTTATATGTAATATATGCTATGTGGTATATAATATATATT T C RFX3 Ensembl:ENSG00000080298 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1197338227 Functional Loss SNV dbSNP153 33..33 33 - - - 43240 RMVar_ID_43240 Human_SNP_ID_387662326 A-to-I Human chr9 - 3504354 3504354 3504354 ATGTGGTATATAATATATATTTTATATACAATATATGCTATGTGGCATATAATATATATTTTATA ATGTGGTATATAATATATATTTTATATACAATGTATGCTATGTGGCATATAATATATATTTTATA T C RFX3 Ensembl:ENSG00000080298 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1391333891 Functional Loss SNV dbSNP153 33..33 33 - - - 43241 RMVar_ID_43241 Human_SNP_ID_387662327 A-to-I Human chr9 - 3504356 3504356 3504356 CTATGTGGTATATAATATATATTTTATATACAATATATGCTATGTGGCATATAATATATATTTTA CTATGTGGTATATAATATATATTTTATATACAGTATATGCTATGTGGCATATAATATATATTTTA T C RFX3 Ensembl:ENSG00000080298 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1427246284 Functional Loss SNV dbSNP153 33..33 33 - - - 43242 RMVar_ID_43242 Human_SNP_ID_387716983 A-to-I Human chr9 + 3690917 3690917 3690917 ATGGCTCACGCAGCCTTGAAATTCTGGGCTCAAATGATCTTCTTGCCTCAGCCTCTTGAGTAGCT ATGGCTCACGCAGCCTTGAAATTCTGGGCTCAGATGATCTTCTTGCCTCAGCCTCTTGAGTAGCT A G RFX3-AS1 Ensembl:ENSG00000232104 lincRNA exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs966821373 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1028854,Human_Splice_Rec_1028855 43243 RMVar_ID_43243 Human_SNP_ID_388059523 A-to-I Human chr9 + 4681458 4681458 4681458 ACTGCCCACCAGAGTTCGAGACCAGCCTGACCAACATGGAGAAACCCTGTCTCTACCAAAAATAC ACTGCCCACCAGAGTTCGAGACCAGCCTGACCGACATGGAGAAACCCTGTCTCTACCAAAAATAC A G CDC37L1 Ensembl:ENSG00000106993 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs970021094 Functional Loss SNV dbSNP153 33..33 33 - - - 43244 RMVar_ID_43244 Human_SNP_ID_388061327 A-to-I Human chr9 + 4687421 4687421 4687421 CAACAAAGGGCCAGGCACAGTGGCTCATGCCTATAATCCCAGCACGTTGGAAGGCCAAGGTGAAG CAACAAAGGGCCAGGCACAGTGGCTCATGCCTGTAATCCCAGCACGTTGGAAGGCCAAGGTGAAG A G CDC37L1 Ensembl:ENSG00000106993 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs938682900 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70550,RMVar_hsa_circ_73189 43245 RMVar_ID_43245 Human_SNP_ID_388061363 A-to-I Human chr9 + 4687514 4687514 4687514 CAGCCTGGGCAACATAGCAAGACCACGTCTCTACAAAAAATTTAAAAATTAGCTGGGTATGGTGG CAGCCTGGGCAACATAGCAAGACCACGTCTCTGCAAAAAATTTAAAAATTAGCTGGGTATGGTGG A G CDC37L1 Ensembl:ENSG00000106993 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1216362887 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70550,RMVar_hsa_circ_73189 43246 RMVar_ID_43246 Human_SNP_ID_388061395 A-to-I Human chr9 + 4687620 4687620 4687620 AGGATCACTTGACCCCAAGAGGTTGAGGCTGCAGTGAGCTATGATTGTGCCACTGTACTCCAGCC AGGATCACTTGACCCCAAGAGGTTGAGGCTGCGGTGAGCTATGATTGTGCCACTGTACTCCAGCC A G CDC37L1 Ensembl:ENSG00000106993 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1027175515 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70550,RMVar_hsa_circ_73189 43247 RMVar_ID_43247 Human_SNP_ID_388063330 A-to-I Human chr9 + 4694314 4694314 4694314 GTTGCCTAGACTGACCTAAAACTCCTGTGCTCAGGTGATTCTCCTGCCTTGGCCTCCCAAAATGC GTTGCCTAGACTGACCTAAAACTCCTGTGCTCGGGTGATTCTCCTGCCTTGGCCTCCCAAAATGC A G CDC37L1 Ensembl:ENSG00000106993 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1026030740 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73189,RMVar_hsa_circ_255430,RMVar_hsa_circ_77379,RMVar_hsa_circ_365743 43248 RMVar_ID_43248 Human_SNP_ID_388068317 A-to-I Human chr9 - 4710802 4710802 4710802 GGGCTCACGCAATTCTTCTACCTCAGCCTCCCAAGTAGCTGAAACTACAGGTATGTACCACCATG GGGCTCACGCAATTCTTCTACCTCAGCCTCCCGAGTAGCTGAAACTACAGGTATGTACCACCATG T C AK3 Ensembl:ENSG00000147853 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs568687184 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_255435,RMVar_hsa_circ_87153 43249 RMVar_ID_43249 Human_SNP_ID_388068325 A-to-I Human chr9 - 4710828 4710828 4710828 TTGGGTCACTGTAACGTTGAACTCCTGGGCTCACGCAATTCTTCTACCTCAGCCTCCCAAGTAGC TTGGGTCACTGTAACGTTGAACTCCTGGGCTCGCGCAATTCTTCTACCTCAGCCTCCCAAGTAGC T C AK3 Ensembl:ENSG00000147853 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1007528486 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_255435,RMVar_hsa_circ_87153 43250 RMVar_ID_43250 Human_SNP_ID_388068344 A-to-I Human chr9 - 4710906 4710906 4710906 CTGTAATACAACTTTTTTCTTTATTTTTTTTTAGACAGGGCCTCACTCTGTTGCCCAGACTAGAG CTGTAATACAACTTTTTTCTTTATTTTTTTTTCGACAGGGCCTCACTCTGTTGCCCAGACTAGAG T G AK3 Ensembl:ENSG00000147853 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs895210964 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_719388,Human_RBP_ID_7929106,Human_RBP_ID_24563582,Human_RBP_ID_26239129,Human_RBP_ID_27786060 RMVar_hsa_circ_255435,RMVar_hsa_circ_87153 43251 RMVar_ID_43251 Human_SNP_ID_388073370 A-to-I Human chr9 - 4724679 4724673 4724679 GACCTCTTGGGCTCAAGCAATCTTCCCACCTCAGTCTCCTGAGTAGCTGAGACTACAGCCATGAG GACCTCTTGGGCTCAAGCAATCTTCCCACCTC______CTGAGTAGCTGAGACTACAGCCATGAG GGAGACT G AK3 Ensembl:ENSG00000147853 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1417474848 Functional Loss DEL dbSNP153 33..38 33 - - - RMVar_hsa_circ_93666,RMVar_hsa_circ_103274,RMVar_hsa_circ_255436,RMVar_hsa_circ_255437 43252 RMVar_ID_43252 Human_SNP_ID_388073376 A-to-I Human chr9 - 4724684 4724684 4724684 GCCTTGACCTCTTGGGCTCAAGCAATCTTCCCACCTCAGTCTCCTGAGTAGCTGAGACTACAGCC GCCTTGACCTCTTGGGCTCAAGCAATCTTCCCGCCTCAGTCTCCTGAGTAGCTGAGACTACAGCC T C AK3 Ensembl:ENSG00000147853 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1197525843 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93666,RMVar_hsa_circ_103274,RMVar_hsa_circ_255436,RMVar_hsa_circ_255437 43253 RMVar_ID_43253 Human_SNP_ID_388073379 A-to-I Human chr9 - 4724693 4724693 4724693 CTCACTGTAGCCTTGACCTCTTGGGCTCAAGCAATCTTCCCACCTCAGTCTCCTGAGTAGCTGAG CTCACTGTAGCCTTGACCTCTTGGGCTCAAGCTATCTTCCCACCTCAGTCTCCTGAGTAGCTGAG T A AK3 Ensembl:ENSG00000147853 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1222237898 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93666,RMVar_hsa_circ_103274,RMVar_hsa_circ_255436,RMVar_hsa_circ_255437 43254 RMVar_ID_43254 Human_SNP_ID_388073380 A-to-I Human chr9 - 4724693 4724693 4724693 CTCACTGTAGCCTTGACCTCTTGGGCTCAAGCAATCTTCCCACCTCAGTCTCCTGAGTAGCTGAG CTCACTGTAGCCTTGACCTCTTGGGCTCAAGCGATCTTCCCACCTCAGTCTCCTGAGTAGCTGAG T C AK3 Ensembl:ENSG00000147853 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1222237898 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93666,RMVar_hsa_circ_103274,RMVar_hsa_circ_255436,RMVar_hsa_circ_255437 43255 RMVar_ID_43255 Human_SNP_ID_388073414 A-to-I Human chr9 - 4724773 4724773 4724773 TTCTATGATTTTTTTTTTTTTCTTTTTGAAACAGGGTCTCACTCCGTTGCCCAGGCGGGAGTGCA TTCTATGATTTTTTTTTTTTTCTTTTTGAAACGGGGTCTCACTCCGTTGCCCAGGCGGGAGTGCA T C AK3 Ensembl:ENSG00000147853 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1313531300 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93666,RMVar_hsa_circ_103274,RMVar_hsa_circ_255436,RMVar_hsa_circ_255437 43256 RMVar_ID_43256 Human_SNP_ID_388074651 A-to-I Human chr9 - 4728414 4728414 4728414 GGCATGCACCACCACACCCAGCTAATTTTTGTATTACTAGTAGAGACAGGGTTTCACCATTTTGG GGCATGCACCACCACACCCAGCTAATTTTTGTGTTACTAGTAGAGACAGGGTTTCACCATTTTGG T C AK3 Ensembl:ENSG00000147853 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs766889602 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16683416,Human_RBP_ID_24304271 RMVar_hsa_circ_103274,RMVar_hsa_circ_255436 43257 RMVar_ID_43257 Human_SNP_ID_388075408 A-to-I Human chr9 - 4729623 4729623 4729623 TGCTGTGTTGCCCAGGCTGGTCAGGAACTCTTAGGCTTGAGCAGTCTTCCTGTGTTGGCTCCCAA TGCTGTGTTGCCCAGGCTGGTCAGGAACTCTTGGGCTTGAGCAGTCTTCCTGTGTTGGCTCCCAA T C AK3 Ensembl:ENSG00000147853 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027986192 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9236753,Human_RBP_ID_16683424,Human_RBP_ID_17579189 RMVar_hsa_circ_103274,RMVar_hsa_circ_255436 43258 RMVar_ID_43258 Human_SNP_ID_388075437 A-to-I Human chr9 - 4729718 4729718 4729718 CACCCAAGTGATACTCCCACCTGAGCCTCCCAAGTAGCTGGGACTACAGGCATGCACCACCATGC CACCCAAGTGATACTCCCACCTGAGCCTCCCATGTAGCTGGGACTACAGGCATGCACCACCATGC T A AK3 Ensembl:ENSG00000147853 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs534706692 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103274,RMVar_hsa_circ_255436 43259 RMVar_ID_43259 Human_SNP_ID_388076256 A-to-I Human chr9 - 4732052 4732052 4732052 CCAGCTACTTGGGAGGTTGAGGTGGGAGGATCACTTGGACCCAGCACGTCGAGGCTGCAGTGAGC CCAGCTACTTGGGAGGTTGAGGTGGGAGGATCTCTTGGACCCAGCACGTCGAGGCTGCAGTGAGC T A AK3 Ensembl:ENSG00000147853 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs897342434 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1227491,Human_RBP_ID_16683480,Human_RBP_ID_26225350 RMVar_hsa_circ_103274,RMVar_hsa_circ_255436 43260 RMVar_ID_43260 Human_SNP_ID_388076603 A-to-I Human chr9 - 4732985 4732985 4732985 AAAAAATTAGCCAGGCATGATTCTGCTTGTCTATAGTCCTAACTACTTGGGAAGCTAAGCTGGGA AAAAAATTAGCCAGGCATGATTCTGCTTGTCTGTAGTCCTAACTACTTGGGAAGCTAAGCTGGGA T C AK3 Ensembl:ENSG00000147853 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10121108 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103274,RMVar_hsa_circ_255436 43261 RMVar_ID_43261 Human_SNP_ID_388077426 A-to-I Human chr9 - 4735150 4735150 4735150 CCTCAAGTAATCCTCCCCTCTTTAGCCTCTCAAGGTGTTGGGATTACAGGCATGAGCCACAGTGC CCTCAAGTAATCCTCCCCTCTTTAGCCTCTCAGGGTGTTGGGATTACAGGCATGAGCCACAGTGC T C AK3 Ensembl:ENSG00000147853 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1488191304 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103274,RMVar_hsa_circ_255436 43262 RMVar_ID_43262 Human_SNP_ID_388077433 A-to-I Human chr9 - 4735184 4735184 4735184 ACCATGTTGGTCCAGGCTTGTCATGAACTCCTAGCCTCAAGTAATCCTCCCCTCTTTAGCCTCTC ACCATGTTGGTCCAGGCTTGTCATGAACTCCTGGCCTCAAGTAATCCTCCCCTCTTTAGCCTCTC T C AK3 Ensembl:ENSG00000147853 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs981771463 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17579041 RMVar_hsa_circ_103274,RMVar_hsa_circ_255436 43263 RMVar_ID_43263 Human_SNP_ID_388077996 A-to-I Human chr9 - 4735871 4735871 4735871 ACCTCAAGTGATCCACCCACCTCGGCTTCTCAAAGTTCTGGGATTACAGGCGTGAGCTACTGCAC ACCTCAAGTGATCCACCCACCTCGGCTTCTCAGAGTTCTGGGATTACAGGCGTGAGCTACTGCAC T C AK3 Ensembl:ENSG00000147853 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs895310200 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103274,RMVar_hsa_circ_255436 43264 RMVar_ID_43264 Human_SNP_ID_388078004 A-to-I Human chr9 - 4735893 4735893 4735893 CCGGGCTGGTCTCGAACTTCCTACCTCAAGTGATCCACCCACCTCGGCTTCTCAAAGTTCTGGGA CCGGGCTGGTCTCGAACTTCCTACCTCAAGTGGTCCACCCACCTCGGCTTCTCAAAGTTCTGGGA T C AK3 Ensembl:ENSG00000147853 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs982609248 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103274,RMVar_hsa_circ_255436 43265 RMVar_ID_43265 Human_SNP_ID_388078036 A-to-I Human chr9 - 4735952 4735952 4735952 AGCCACCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTAGCCGGGC AGCCACCATGCCCAGCTAATTTTTGTATTTTTGGTAGAGATGGGGTTTCACCATGTTAGCCGGGC T C AK3 Ensembl:ENSG00000147853 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1390799654 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103274,RMVar_hsa_circ_255436 43266 RMVar_ID_43266 Human_SNP_ID_388078430 A-to-I Human chr9 - 4736973 4736973 4736973 GCATAGTGCGTCTCAGAGACATAACCCTGGCTAGGTGTGGTGGCTTATGCCTGTAATCTCAACAC GCATAGTGCGTCTCAGAGACATAACCCTGGCTGGGTGTGGTGGCTTATGCCTGTAATCTCAACAC T C AK3 Ensembl:ENSG00000147853 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1489775607 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16683574 RMVar_hsa_circ_103274,RMVar_hsa_circ_255436 43267 RMVar_ID_43267 Human_SNP_ID_388078595 A-to-I Human chr9 - 4737385 4737385 4737385 AACAGTATTTATTGGGGGATTAGGGTGAAAACATAGATTTCTCCATGTTAAATACTCTTTTCTCT AACAGTATTTATTGGGGGATTAGGGTGAAAACTTAGATTTCTCCATGTTAAATACTCTTTTCTCT T A AK3 Ensembl:ENSG00000147853 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs439786 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_4987,GWAS_ID_4988,GWAS_ID_4989,GWAS_ID_4990 RMVar_hsa_circ_103274,RMVar_hsa_circ_255436 43268 RMVar_ID_43268 Human_SNP_ID_388078596 A-to-I Human chr9 - 4737385 4737385 4737385 AACAGTATTTATTGGGGGATTAGGGTGAAAACATAGATTTCTCCATGTTAAATACTCTTTTCTCT AACAGTATTTATTGGGGGATTAGGGTGAAAACGTAGATTTCTCCATGTTAAATACTCTTTTCTCT T C AK3 Ensembl:ENSG00000147853 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs439786 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_4987,GWAS_ID_4988,GWAS_ID_4989,GWAS_ID_4990 RMVar_hsa_circ_103274,RMVar_hsa_circ_255436 43269 RMVar_ID_43269 Human_SNP_ID_388078645 A-to-I Human chr9 - 4737535 4737535 4737535 TAATTTATTTTCAGTAGAGATGGTTTTGCCGTATTGGCAGGCTGGTCTCGAACTCCTGACCTCAG TAATTTATTTTCAGTAGAGATGGTTTTGCCGTTTTGGCAGGCTGGTCTCGAACTCCTGACCTCAG T A AK3 Ensembl:ENSG00000147853 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs578161274 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17579194 RMVar_hsa_circ_103274,RMVar_hsa_circ_255436 43270 RMVar_ID_43270 Human_SNP_ID_388078683 A-to-I Human chr9 - 4737632 4737632 4737632 TTACTGCGACCTCCGACTCCTGGGTTCAAGCGATTCTCCTGCTTCAGCTTCCGAACTCAGGTAGC TTACTGCGACCTCCGACTCCTGGGTTCAAGCGGTTCTCCTGCTTCAGCTTCCGAACTCAGGTAGC T C AK3 Ensembl:ENSG00000147853 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904872617 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26225403 RMVar_hsa_circ_103274,RMVar_hsa_circ_255436 43271 RMVar_ID_43271 Human_SNP_ID_388078857 A-to-I Human chr9 - 4738140 4738140 4738140 ATGTTTAATTTTATCAAAGTTGTATAGTTATTAAACATTTTTATTGGACGCGTATGTTGTTAACT ATGTTTAATTTTATCAAAGTTGTATAGTTATTTAACATTTTTATTGGACGCGTATGTTGTTAACT T A AK3 Ensembl:ENSG00000147853 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1286176666 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1705485,Human_RBP_ID_2064885,Human_RBP_ID_3900840,Human_RBP_ID_8705197,Human_RBP_ID_17642587,Human_RBP_ID_18398991 RMVar_hsa_circ_103274,RMVar_hsa_circ_255436 43272 RMVar_ID_43272 Human_SNP_ID_388078858 A-to-I Human chr9 - 4738140 4738140 4738140 ATGTTTAATTTTATCAAAGTTGTATAGTTATTAAACATTTTTATTGGACGCGTATGTTGTTAACT ATGTTTAATTTTATCAAAGTTGTATAGTTATTGAACATTTTTATTGGACGCGTATGTTGTTAACT T C AK3 Ensembl:ENSG00000147853 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1286176666 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1705485,Human_RBP_ID_2064885,Human_RBP_ID_3900840,Human_RBP_ID_8705197,Human_RBP_ID_17642587,Human_RBP_ID_18398991 RMVar_hsa_circ_103274,RMVar_hsa_circ_255436 43273 RMVar_ID_43273 Human_SNP_ID_388078895 A-to-I Human chr9 - 4738231 4738231 4738231 AAACTGGGAGGCGGAGGTTGCAGCGAGCCGAGATGGCGCCATTGCATTCCAGCCTAGGTGAAAAG AAACTGGGAGGCGGAGGTTGCAGCGAGCCGAGTTGGCGCCATTGCATTCCAGCCTAGGTGAAAAG T A AK3 Ensembl:ENSG00000147853 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1343876186 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17579196 RMVar_hsa_circ_103274,RMVar_hsa_circ_255436 43274 RMVar_ID_43274 Human_SNP_ID_388078960 A-to-I Human chr9 - 4738400 4738400 4738400 GCACTTTGGGAGGCTGAGGTGGGTGAATCACCAGAGGTCAGGAGTTCAAGACCAGCCTGGCCAAC GCACTTTGGGAGGCTGAGGTGGGTGAATCACCCGAGGTCAGGAGTTCAAGACCAGCCTGGCCAAC T G AK3 Ensembl:ENSG00000147853 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1382516976 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103274,RMVar_hsa_circ_255436 43275 RMVar_ID_43275 Human_SNP_ID_388079142 A-to-I Human chr9 - 4738887 4738887 4738887 CGCGCCTGTGGTCCCAGCTTCTCTGGAGGCTGAGGTGGGAGTATCACTTGAGCCCGGGATGCAGA CGCGCCTGTGGTCCCAGCTTCTCTGGAGGCTGGGGTGGGAGTATCACTTGAGCCCGGGATGCAGA T C AK3 Ensembl:ENSG00000147853 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1455276799 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103274,RMVar_hsa_circ_255436 43276 RMVar_ID_43276 Human_SNP_ID_388079159 A-to-I Human chr9 - 4738928 4738928 4738928 TCTCTACCAAAAATACAAAAAATTAGCTGGGCATGGTGGCTCGCGCCTGTGGTCCCAGCTTCTCT TCTCTACCAAAAATACAAAAAATTAGCTGGGCGTGGTGGCTCGCGCCTGTGGTCCCAGCTTCTCT T C AK3 Ensembl:ENSG00000147853 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs559405849 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103274,RMVar_hsa_circ_255436 43277 RMVar_ID_43277 Human_SNP_ID_388079330 A-to-I Human chr9 - 4739355 4739355 4739355 ACTGCGTCTCTATAAAAAATTCAAAAACAATTAGCGAGGCGCAGTGGCAGGCACCTGTGATCCTA ACTGCGTCTCTATAAAAAATTCAAAAACAATTGGCGAGGCGCAGTGGCAGGCACCTGTGATCCTA T C AK3 Ensembl:ENSG00000147853 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1296289449 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18136584 RMVar_hsa_circ_103274,RMVar_hsa_circ_255436 43278 RMVar_ID_43278 Human_SNP_ID_388079489 A-to-I Human chr9 - 4739767 4739767 4739767 GCCACCACGCCGGGCTAATTTTTTGTATTTTTAGTAGCGATGGGGTTTCACTGTGTTAGCCAGGC GCCACCACGCCGGGCTAATTTTTTGTATTTTTGGTAGCGATGGGGTTTCACTGTGTTAGCCAGGC T C AK3 Ensembl:ENSG00000147853 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs747817308 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16683635,Human_RBP_ID_26225428 RMVar_hsa_circ_103274,RMVar_hsa_circ_255436 43279 RMVar_ID_43279 Human_SNP_ID_388079529 A-to-I Human chr9 - 4739845 4739845 4739845 AGTCTTGCTCTGTCTGCCTCCTGGGTTCAAGCAATTCTCCTGTCTCAGCCTCCCTAGTAGCTGGG AGTCTTGCTCTGTCTGCCTCCTGGGTTCAAGCCATTCTCCTGTCTCAGCCTCCCTAGTAGCTGGG T G AK3 Ensembl:ENSG00000147853 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1445915098 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16683637 RMVar_hsa_circ_103274,RMVar_hsa_circ_255436 43280 RMVar_ID_43280 Human_SNP_ID_388100007 A-to-I Human chr9 - 4799768 4799768 4799768 ATTACCCACTCCCAACCCAGGGAGGTAGTGACAAAAAATAAAAATACAGGACTCATTCAAGGCCC ATTACCCACTCCCAACCCAGGGAGGTAGTGACGAAAAATAAAAATACAGGACTCATTCAAGGCCC T C RF01960-016 RNACentral:URS0000907730 rRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs75535436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5271434,Human_RBP_ID_5431484,Human_RBP_ID_5454835,Human_RBP_ID_5482152,Human_RBP_ID_5516218,Human_RBP_ID_7957696,Human_RBP_ID_8158472,Human_RBP_ID_8928760,Human_RBP_ID_17057363,Human_RBP_ID_17716646,Human_RBP_ID_18136589,Human_RBP_ID_18203416,Human_RBP_ID_18398994,Human_RBP_ID_22424926,Human_RBP_ID_23300832 43281 RMVar_ID_43281 Human_SNP_ID_388100013 A-to-I Human chr9 - 4799782 4799782 4799782 TAGCAAGCATGCAAATTACCCACTCCCAACCCAGGGAGGTAGTGACAAAAAATAAAAATACAGGA TAGCAAGCATGCAAATTACCCACTCCCAACCCGGGGAGGTAGTGACAAAAAATAAAAATACAGGA T C RF01960-016 RNACentral:URS0000907730 rRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs79618092 Functional Loss SNV dbSNP153 33..33 33 - - - 43282 RMVar_ID_43282 Human_SNP_ID_388100015 A-to-I Human chr9 - 4799787 4799787 4799787 GAAGGTAGCAAGCATGCAAATTACCCACTCCCAACCCAGGGAGGTAGTGACAAAAAATAAAAATA GAAGGTAGCAAGCATGCAAATTACCCACTCCCGACCCAGGGAGGTAGTGACAAAAAATAAAAATA T C RF01960-016 RNACentral:URS0000907730 rRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs80077609 Functional Loss SNV dbSNP153 33..33 33 - - - 43283 RMVar_ID_43283 Human_SNP_ID_388100019 A-to-I Human chr9 - 4799806 4799806 4799806 AATGGCTACCACATCCAAGGAAGGTAGCAAGCATGCAAATTACCCACTCCCAACCCAGGGAGGTA AATGGCTACCACATCCAAGGAAGGTAGCAAGCCTGCAAATTACCCACTCCCAACCCAGGGAGGTA T G RF01960-016 RNACentral:URS0000907730 rRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs911654855 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1059428,Human_RBP_ID_5431485,Human_RBP_ID_5454566,Human_RBP_ID_5482153,Human_RBP_ID_5516219,Human_RBP_ID_7929308,Human_RBP_ID_16683792,Human_RBP_ID_18141759,Human_RBP_ID_22518379,Human_RBP_ID_27162582,Human_RBP_ID_27546407 43284 RMVar_ID_43284 Human_SNP_ID_388100020 A-to-I Human chr9 - 4799809 4799809 4799809 AGAAATGGCTACCACATCCAAGGAAGGTAGCAAGCATGCAAATTACCCACTCCCAACCCAGGGAG AGAAATGGCTACCACATCCAAGGAAGGTAGCAGGCATGCAAATTACCCACTCCCAACCCAGGGAG T C RF01960-016 RNACentral:URS0000907730 rRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs182167252 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1059428,Human_RBP_ID_5431485,Human_RBP_ID_5454566,Human_RBP_ID_5482153,Human_RBP_ID_5516219,Human_RBP_ID_7929308,Human_RBP_ID_16683792,Human_RBP_ID_18141759,Human_RBP_ID_22518379,Human_RBP_ID_27162582,Human_RBP_ID_27546407 43285 RMVar_ID_43285 Human_SNP_ID_388110979 A-to-I Human chr9 + 4831610 4831610 4831610 GTGATCCTCCCACCTCAGCCTCTCAAGTAGCTAGGACCACAGGCGTGCAGCATGCCCAGCTTATT GTGATCCTCCCACCTCAGCCTCTCAAGTAGCTGGGACCACAGGCGTGCAGCATGCCCAGCTTATT A G RCL1 Ensembl:ENSG00000120158 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1406438829 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_255448 43286 RMVar_ID_43286 Human_SNP_ID_388189174 A-to-I Human chr9 + 5085751 5085751 5085751 ATTTCTGCAATTAAGGCTGTGGCGCGCTGGCTAGCTTGCACATGTCGGGAGTTATTATGATGAAT ATTTCTGCAATTAAGGCTGTGGCGCGCTGGCTGGCTTGCACATGTCGGGAGTTATTATGATGAAT A G JAK2 Ensembl:ENSG00000096968 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1344977675 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16685276 RMVar_hsa_circ_335183,RMVar_hsa_circ_344758,RMVar_hsa_circ_56133,RMVar_hsa_circ_255458,RMVar_hsa_circ_278573,RMVar_hsa_circ_13577,RMVar_hsa_circ_255473,RMVar_hsa_circ_360137,RMVar_hsa_circ_361960,RMVar_hsa_circ_62686,RMVar_hsa_circ_255478,RMVar_hsa_circ_350842,RMVar_hsa_circ_367023,RMVar_hsa_circ_338702,RMVar_hsa_circ_286777,RMVar_hsa_circ_26078,RMVar_hsa_circ_10503,RMVar_hsa_circ_255480,RMVar_hsa_circ_69880,RMVar_hsa_circ_32049,RMVar_hsa_circ_295860,RMVar_hsa_circ_74629,RMVar_hsa_circ_255481 43287 RMVar_ID_43287 Human_SNP_ID_388198770 A-to-I Human chr9 + 5112729 5112729 5112729 CAGCAAGTGCGAGAGCGGAACCTGAATCCCAAAACAGCCTGTTTGAAACGGCGAGAAGAGAAGGT CAGCAAGTGCGAGAGCGGAACCTGAATCCCAAGACAGCCTGTTTGAAACGGCGAGAAGAGAAGGT A G TCF3P1,JAK2 Ensembl:ENSG00000236567,Ensembl:ENSG00000096968 Pseudogene,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1457656600 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17438349,Human_RBP_ID_26563983 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 43288 RMVar_ID_43288 Human_SNP_ID_388289386 A-to-I Human chr9 - 5399811 5399811 5399811 AATTTTTGGTATTTTTAGTAGCGACGTAGTTTAGCCATGTTGGCCAGGCTGGTCTCAAACTCCTG AATTTTTGGTATTTTTAGTAGCGACGTAGTTTCGCCATGTTGGCCAGGCTGGTCTCAAACTCCTG T G PLGRKT Ensembl:ENSG00000107020 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1402953823 Functional Loss SNV dbSNP153 33..33 33 - - - 43289 RMVar_ID_43289 Human_SNP_ID_388385642 A-to-I Human chr9 + 5702781 5702781 5702781 GTTGCCCAGGCTGGTCTCGAACTCCTGAGCTCAGGCATTCTGCCCGACTTGGCCTCCCAAAGTGC GTTGCCCAGGCTGGTCTCGAACTCCTGAGCTCGGGCATTCTGCCCGACTTGGCCTCCCAAAGTGC A G RIC1 Ensembl:ENSG00000107036 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1302474244 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80491,RMVar_hsa_circ_255485,RMVar_hsa_circ_94782,RMVar_hsa_circ_305606,RMVar_hsa_circ_116147,RMVar_hsa_circ_255490,RMVar_hsa_circ_255491,RMVar_hsa_circ_255492,RMVar_hsa_circ_100941,RMVar_hsa_circ_360223,RMVar_hsa_circ_297089,RMVar_hsa_circ_255494,RMVar_hsa_circ_50331,RMVar_hsa_circ_255495 43290 RMVar_ID_43290 Human_SNP_ID_388385663 A-to-I Human chr9 + 5702815 5702815 5702815 GCATTCTGCCCGACTTGGCCTCCCAAAGTGCTAGGATTACAGGCGTGAGCCACTGCATGCAACTG GCATTCTGCCCGACTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCATGCAACTG A G RIC1 Ensembl:ENSG00000107036 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs376273195 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80491,RMVar_hsa_circ_255485,RMVar_hsa_circ_94782,RMVar_hsa_circ_305606,RMVar_hsa_circ_116147,RMVar_hsa_circ_255490,RMVar_hsa_circ_255491,RMVar_hsa_circ_255492,RMVar_hsa_circ_100941,RMVar_hsa_circ_360223,RMVar_hsa_circ_297089,RMVar_hsa_circ_255494,RMVar_hsa_circ_50331,RMVar_hsa_circ_255495 43291 RMVar_ID_43291 Human_SNP_ID_388389921 A-to-I Human chr9 + 5716022 5716022 5716022 ACACGTCACAGCACGCTAATTTTTTGTACTTTATTGTAGAGACAAGGTTTCACCATGTTGTTGAG ACACGTCACAGCACGCTAATTTTTTGTACTTTGTTGTAGAGACAAGGTTTCACCATGTTGTTGAG A G RIC1 Ensembl:ENSG00000107036 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs143732782 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43546,RMVar_hsa_circ_80491,RMVar_hsa_circ_255485,RMVar_hsa_circ_94782,RMVar_hsa_circ_305606,RMVar_hsa_circ_255491,RMVar_hsa_circ_255492,RMVar_hsa_circ_100941,RMVar_hsa_circ_360223,RMVar_hsa_circ_297089,RMVar_hsa_circ_255494,RMVar_hsa_circ_50331,RMVar_hsa_circ_255495,RMVar_hsa_circ_368339,RMVar_hsa_circ_309029 43292 RMVar_ID_43292 Human_SNP_ID_388389934 A-to-I Human chr9 + 5716044 5716044 5716044 TTTGTACTTTATTGTAGAGACAAGGTTTCACCATGTTGTTGAGGCTGGTCTCAAACTCCTAAGCT TTTGTACTTTATTGTAGAGACAAGGTTTCACCGTGTTGTTGAGGCTGGTCTCAAACTCCTAAGCT A G RIC1 Ensembl:ENSG00000107036 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1033556392 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43546,RMVar_hsa_circ_80491,RMVar_hsa_circ_255485,RMVar_hsa_circ_94782,RMVar_hsa_circ_305606,RMVar_hsa_circ_255491,RMVar_hsa_circ_255492,RMVar_hsa_circ_100941,RMVar_hsa_circ_360223,RMVar_hsa_circ_297089,RMVar_hsa_circ_255494,RMVar_hsa_circ_50331,RMVar_hsa_circ_255495,RMVar_hsa_circ_368339,RMVar_hsa_circ_309029 43293 RMVar_ID_43293 Human_SNP_ID_388389947 A-to-I Human chr9 + 5716072 5716072 5716072 CACCATGTTGTTGAGGCTGGTCTCAAACTCCTAAGCTCAAGCGATCTCCCCTCCTTGGCCTCTCA CACCATGTTGTTGAGGCTGGTCTCAAACTCCTTAGCTCAAGCGATCTCCCCTCCTTGGCCTCTCA A T RIC1 Ensembl:ENSG00000107036 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs373183168 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43546,RMVar_hsa_circ_80491,RMVar_hsa_circ_255485,RMVar_hsa_circ_94782,RMVar_hsa_circ_305606,RMVar_hsa_circ_255491,RMVar_hsa_circ_255492,RMVar_hsa_circ_100941,RMVar_hsa_circ_360223,RMVar_hsa_circ_297089,RMVar_hsa_circ_255494,RMVar_hsa_circ_50331,RMVar_hsa_circ_255495,RMVar_hsa_circ_368339,RMVar_hsa_circ_309029 43294 RMVar_ID_43294 Human_SNP_ID_388420184 A-to-I Human chr9 - 5807738 5807736 5807738 CCGTTTTTTTTTTGTTGTTGTTGTTGAGACAGAGTCTCACTCTGTCGCCCAGGTTGGAGTGCAGT CCGTTTTTTTTTTGTTGTTGTTGTTGAGACAG__TCTCACTCTGTCGCCCAGGTTGGAGTGCAGT ACT A ERMP1 Ensembl:ENSG00000099219 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232711483 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_36671,RMVar_hsa_circ_339627,RMVar_hsa_circ_287119,RMVar_hsa_circ_54857,RMVar_hsa_circ_267702,RMVar_hsa_circ_255514,RMVar_hsa_circ_357731,RMVar_hsa_circ_337994,RMVar_hsa_circ_282228,RMVar_hsa_circ_255515,RMVar_hsa_circ_255517 43295 RMVar_ID_43295 Human_SNP_ID_388454316 A-to-I Human chr9 - 5918535 5918535 5918535 CTAATTTTTTAATTTTTTGTAGAGATGGTTTCACCATGTTGCTAGGCTGGTCTTGAACTCCTGGT CTAATTTTTTAATTTTTTGTAGAGATGGTTTCGCCATGTTGCTAGGCTGGTCTTGAACTCCTGGT T C KIAA2026 Ensembl:ENSG00000183354 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1187979271 Functional Loss SNV dbSNP153 33..33 33 - - - 43296 RMVar_ID_43296 Human_SNP_ID_388454317 A-to-I Human chr9 - 5918535 5918535 5918535 CTAATTTTTTAATTTTTTGTAGAGATGGTTTCACCATGTTGCTAGGCTGGTCTTGAACTCCTGGT CTAATTTTTTAATTTTTTGTAGAGATGGTTTCCCCATGTTGCTAGGCTGGTCTTGAACTCCTGGT T G KIAA2026 Ensembl:ENSG00000183354 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1187979271 Functional Loss SNV dbSNP153 33..33 33 - - - 43297 RMVar_ID_43297 Human_SNP_ID_388454395 A-to-I Human chr9 - 5918710 5918710 5918710 AGCCATCCTCCCACCTCAGCCCCCCAAGTATTAGGTTGGTGTGTAAGTAATTGTGGTTTTTTTGC AGCCATCCTCCCACCTCAGCCCCCCAAGTATTTGGTTGGTGTGTAAGTAATTGTGGTTTTTTTGC T A KIAA2026 Ensembl:ENSG00000183354 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559097773 Functional Loss SNV dbSNP153 33..33 33 - - - 43298 RMVar_ID_43298 Human_SNP_ID_388461902 A-to-I Human chr9 - 5940348 5940348 5940348 TCTACAAAAAATACAAAAATTAGCCAGGCTGTAGTGGCGCGTGCCTGTAATCCCAGCTACTCGGG TCTACAAAAAATACAAAAATTAGCCAGGCTGTGGTGGCGCGTGCCTGTAATCCCAGCTACTCGGG T C KIAA2026 Ensembl:ENSG00000183354 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202345698 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20386,RMVar_hsa_circ_311621,RMVar_hsa_circ_29432,RMVar_hsa_circ_255532,RMVar_hsa_circ_361229,RMVar_hsa_circ_64085,RMVar_hsa_circ_323552 43299 RMVar_ID_43299 Human_SNP_ID_388483187 A-to-I Human chr9 - 6007282 6007282 6007282 GGCGGACTTCAGGTTGATGCTGGAGACGTGCTACCGCCTGCACGGAGTGGACCACTGGATCTCCA GGCGGACTTCAGGTTGATGCTGGAGACGTGCTGCCGCCTGCACGGAGTGGACCACTGGATCTCCA T C KIAA2026 Ensembl:ENSG00000183354 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1458584181 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19024777 Human_Splice_Rec_1029981,Human_Splice_Rec_1029993,Human_Splice_Rec_1030019 43300 RMVar_ID_43300 Human_SNP_ID_388610746 A-to-I Human chr9 + 6427022 6427022 6427022 CACCTGCCTCGGCCTCCCAAAGTGCTGGGATTATAGGCATGAGCCACTGTGCCTGGCTTGAATTA CACCTGCCTCGGCCTCCCAAAGTGCTGGGATTGTAGGCATGAGCCACTGTGCCTGGCTTGAATTA A G UHRF2 Ensembl:ENSG00000147854 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs111254887 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_255541,RMVar_hsa_circ_75809,RMVar_hsa_circ_118973,RMVar_hsa_circ_290597,RMVar_hsa_circ_123875,RMVar_hsa_circ_255540,RMVar_hsa_circ_369474,RMVar_hsa_circ_282515,RMVar_hsa_circ_126442,RMVar_hsa_circ_98120,RMVar_hsa_circ_111169,RMVar_hsa_circ_76001,RMVar_hsa_circ_255545,RMVar_hsa_circ_255547,RMVar_hsa_circ_255549,RMVar_hsa_circ_65341,RMVar_hsa_circ_255548,RMVar_hsa_circ_255546,RMVar_hsa_circ_255543,RMVar_hsa_circ_255544,RMVar_hsa_circ_255542 43301 RMVar_ID_43301 Human_SNP_ID_388622557 A-to-I Human chr9 + 6463062 6463062 6463062 CCAGCACTTTGGGAGGCCAGGGTGGGTGGATCACCTGAGGTCAGGAGATCGAGACCAGTCTGACC CCAGCACTTTGGGAGGCCAGGGTGGGTGGATCCCCTGAGGTCAGGAGATCGAGACCAGTCTGACC A C UHRF2 Ensembl:ENSG00000147854 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1343119596 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_255541,RMVar_hsa_circ_75809,RMVar_hsa_circ_118973,RMVar_hsa_circ_369474,RMVar_hsa_circ_126442,RMVar_hsa_circ_98120,RMVar_hsa_circ_111169,RMVar_hsa_circ_76001,RMVar_hsa_circ_255545,RMVar_hsa_circ_255547,RMVar_hsa_circ_65341,RMVar_hsa_circ_255548,RMVar_hsa_circ_255546,RMVar_hsa_circ_255543,RMVar_hsa_circ_255544,RMVar_hsa_circ_255542,RMVar_hsa_circ_274664,RMVar_hsa_circ_376480,RMVar_hsa_circ_268227,RMVar_hsa_circ_73673,RMVar_hsa_circ_107411,RMVar_hsa_circ_373809,RMVar_hsa_circ_65636,RMVar_hsa_circ_255552,RMVar_hsa_circ_24117,RMVar_hsa_circ_24141,RMVar_hsa_circ_255553 43302 RMVar_ID_43302 Human_SNP_ID_388629092 A-to-I Human chr9 + 6482701 6482701 6482701 TCACTGCAAGCTCTGCCTCGTGGGTTCACGCCATTCTCCTGCCTCAGCCTCCAAAGTAGCTGGGA TCACTGCAAGCTCTGCCTCGTGGGTTCACGCCGTTCTCCTGCCTCAGCCTCCAAAGTAGCTGGGA A G UHRF2 Ensembl:ENSG00000147854 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs550445955 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_255541,RMVar_hsa_circ_75809,RMVar_hsa_circ_118973,RMVar_hsa_circ_126442,RMVar_hsa_circ_111169,RMVar_hsa_circ_65341,RMVar_hsa_circ_255543,RMVar_hsa_circ_255544,RMVar_hsa_circ_255542,RMVar_hsa_circ_114661,RMVar_hsa_circ_376480,RMVar_hsa_circ_73673,RMVar_hsa_circ_107411,RMVar_hsa_circ_373809,RMVar_hsa_circ_255552,RMVar_hsa_circ_24141,RMVar_hsa_circ_255553,RMVar_hsa_circ_273136,RMVar_hsa_circ_314487,RMVar_hsa_circ_342101,RMVar_hsa_circ_328362,RMVar_hsa_circ_255564,RMVar_hsa_circ_255555,RMVar_hsa_circ_255557,RMVar_hsa_circ_255556,RMVar_hsa_circ_282524,RMVar_hsa_circ_342138,RMVar_hsa_circ_357817,RMVar_hsa_circ_363780,RMVar_hsa_circ_345422,RMVar_hsa_circ_310159,RMVar_hsa_circ_255562,RMVar_hsa_circ_255563,RMVar_hsa_circ_255561,RMVar_hsa_circ_18394,RMVar_hsa_circ_368192,RMVar_hsa_circ_43683 43303 RMVar_ID_43303 Human_SNP_ID_388631205 A-to-I Human chr9 + 6488122 6488122 6488122 GAAATTAGCTGGGTGTGGTGGCATGTGCCTGTAGTCCCGGCTACCCAGGAGGATGAGGCAGGAGG GAAATTAGCTGGGTGTGGTGGCATGTGCCTGTGGTCCCGGCTACCCAGGAGGATGAGGCAGGAGG A G UHRF2 Ensembl:ENSG00000147854 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909692565 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_255541,RMVar_hsa_circ_75809,RMVar_hsa_circ_118973,RMVar_hsa_circ_126442,RMVar_hsa_circ_111169,RMVar_hsa_circ_255543,RMVar_hsa_circ_255544,RMVar_hsa_circ_255542,RMVar_hsa_circ_114661,RMVar_hsa_circ_73673,RMVar_hsa_circ_107411,RMVar_hsa_circ_373809,RMVar_hsa_circ_255552,RMVar_hsa_circ_255553,RMVar_hsa_circ_314487,RMVar_hsa_circ_342101,RMVar_hsa_circ_328362,RMVar_hsa_circ_255564,RMVar_hsa_circ_255555,RMVar_hsa_circ_255556,RMVar_hsa_circ_342138,RMVar_hsa_circ_357817,RMVar_hsa_circ_363780,RMVar_hsa_circ_345422,RMVar_hsa_circ_310159,RMVar_hsa_circ_255562,RMVar_hsa_circ_255563,RMVar_hsa_circ_18394,RMVar_hsa_circ_368192,RMVar_hsa_circ_43683,RMVar_hsa_circ_255565,RMVar_hsa_circ_34722,RMVar_hsa_circ_299043 43304 RMVar_ID_43304 Human_SNP_ID_388642902 A-to-I Human chr9 + 6524026 6524026 6524026 AGAGACCTGGCCAGGCATGGTGGCTCACGCCTATAATCCCAGCACTCTGGGAGGCCAAGGTGGGA AGAGACCTGGCCAGGCATGGTGGCTCACGCCTGTAATCCCAGCACTCTGGGAGGCCAAGGTGGGA A G RF00017-1068,RF00017-4630 RNACentral:URS0000915CF4,RNACentral:URS000096585E SRP RNA,SRP RNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs200186442 Functional Loss SNV dbSNP153 33..33 33 - - - 43305 RMVar_ID_43305 Human_SNP_ID_388649117 A-to-I Human chr9 - 6541764 6541764 6541764 GCAGTGCAGTGGTGCCATCTCGGCTCACTGCAACCACCACCTTCCAGGTTCAAGCAATTCTCTCA GCAGTGCAGTGGTGCCATCTCGGCTCACTGCAGCCACCACCTTCCAGGTTCAAGCAATTCTCTCA T C GLDC Ensembl:ENSG00000178445 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs543396020 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45962,RMVar_hsa_circ_126110,RMVar_hsa_circ_255571,RMVar_hsa_circ_79387,RMVar_hsa_circ_83749,RMVar_hsa_circ_77585,RMVar_hsa_circ_255569,RMVar_hsa_circ_255570,RMVar_hsa_circ_255568 43306 RMVar_ID_43306 Human_SNP_ID_388686801 A-to-I Human chr9 + 6646928 6646922 6646928 CAGGCACGTGCCACCACGGCCGGCCATTTTTTATTTTTATTTTTAGTAGAGACGGGGTTTCACCG CAGGCACGTGCCACCACGGCCGGCCAT______TTTTTATTTTTAGTAGAGACGGGGTTTCACCG TTTTTTA T AL162411.1 Ensembl:ENSG00000236924 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1336862081 Functional Loss DEL dbSNP153 28..33 33 - - - 43307 RMVar_ID_43307 Human_SNP_ID_388686803 A-to-I Human chr9 + 6646928 6646923 6646928 CAGGCACGTGCCACCACGGCCGGCCATTTTTTATTTTTATTTTTAGTAGAGACGGGGTTTCACCG CAGGCACGTGCCACCACGGCCGGCCATT_____TTTTTATTTTTAGTAGAGACGGGGTTTCACCG TTTTTA T AL162411.1 Ensembl:ENSG00000236924 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1266764553 Functional Loss DEL dbSNP153 29..33 33 - - - 43308 RMVar_ID_43308 Human_SNP_ID_388686805 A-to-I Human chr9 + 6646928 6646928 6646928 CAGGCACGTGCCACCACGGCCGGCCATTTTTTATTTTTATTTTTAGTAGAGACGGGGTTTCACCG CAGGCACGTGCCACCACGGCCGGCCATTTTTTGTTTTTATTTTTAGTAGAGACGGGGTTTCACCG A G AL162411.1 Ensembl:ENSG00000236924 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs184435921 Functional Loss SNV dbSNP153 33..33 33 - - - 43309 RMVar_ID_43309 Human_SNP_ID_388687157 A-to-I Human chr9 + 6647841 6647841 6647841 CTTGAGGACAGGAGTTCAAGACCAGCTTGGCCAAGATGGCGAAACTCAATCTCTACTACAAATAT CTTGAGGACAGGAGTTCAAGACCAGCTTGGCCGAGATGGCGAAACTCAATCTCTACTACAAATAT A G AL162411.1 Ensembl:ENSG00000236924 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1419183497 Functional Loss SNV dbSNP153 33..33 33 - - - 43310 RMVar_ID_43310 Human_SNP_ID_388688002 A-to-I Human chr9 + 6649684 6649684 6649684 TCAAGCAATTCTCCTGCCTCAGCCTCCAGAGTAGCAGGGACTACAGGCATATGCCACCACACGCA TCAAGCAATTCTCCTGCCTCAGCCTCCAGAGTCGCAGGGACTACAGGCATATGCCACCACACGCA A C AL162411.1 Ensembl:ENSG00000236924 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1004377312 Functional Loss SNV dbSNP153 33..33 33 - - - 43311 RMVar_ID_43311 Human_SNP_ID_388688011 A-to-I Human chr9 + 6649700 6649700 6649700 CCTCAGCCTCCAGAGTAGCAGGGACTACAGGCATATGCCACCACACGCACTAATTTTTGTGTTTT CCTCAGCCTCCAGAGTAGCAGGGACTACAGGCGTATGCCACCACACGCACTAATTTTTGTGTTTT A G AL162411.1 Ensembl:ENSG00000236924 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1321120078 Functional Loss SNV dbSNP153 33..33 33 - - - 43312 RMVar_ID_43312 Human_SNP_ID_388688625 A-to-I Human chr9 + 6651131 6651131 6651131 TCTGTAGTCTCAGCTACTTGGGAGGCTGAGGCAGAGAATCGCTGGAACCTGGGAGGTGGAGGTTG TCTGTAGTCTCAGCTACTTGGGAGGCTGAGGCGGAGAATCGCTGGAACCTGGGAGGTGGAGGTTG A G AL162411.1 Ensembl:ENSG00000236924 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1372008668 Functional Loss SNV dbSNP153 33..33 33 - - - 43313 RMVar_ID_43313 Human_SNP_ID_388690172 A-to-I Human chr9 + 6655342 6655342 6655342 CACAGTTTCACTCTTGTTGCCCAGGCTGTAGTACAGTGGCGCGATCTCAGCTCACCACAACCTCC CACAGTTTCACTCTTGTTGCCCAGGCTGTAGTGCAGTGGCGCGATCTCAGCTCACCACAACCTCC A G AL162411.1 Ensembl:ENSG00000236924 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs890228245 Functional Loss SNV dbSNP153 33..33 33 - - - 43314 RMVar_ID_43314 Human_SNP_ID_388690173 A-to-I Human chr9 + 6655342 6655342 6655342 CACAGTTTCACTCTTGTTGCCCAGGCTGTAGTACAGTGGCGCGATCTCAGCTCACCACAACCTCC CACAGTTTCACTCTTGTTGCCCAGGCTGTAGTTCAGTGGCGCGATCTCAGCTCACCACAACCTCC A T AL162411.1 Ensembl:ENSG00000236924 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs890228245 Functional Loss SNV dbSNP153 33..33 33 - - - 43315 RMVar_ID_43315 Human_SNP_ID_388699695 A-to-I Human chr9 + 6682390 6682390 6682390 AATGCAGGCAGGGCGCAGTGGCTCATGCCTGTAAACCGAGCACTTTCGGAGGCCAAGGTGGGCGG AATGCAGGCAGGGCGCAGTGGCTCATGCCTGTGAACCGAGCACTTTCGGAGGCCAAGGTGGGCGG A G RF00017-1068 RNACentral:URS0000915CF4 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1044897286 Functional Loss SNV dbSNP153 33..33 33 - - - 43316 RMVar_ID_43316 Human_SNP_ID_388701570 A-to-I Human chr9 + 6687418 6687418 6687418 AAATTCCCAAACTCAAAGGATCGTCCTGCCTCAGCCACCTAAAGTGCTGGGATTACAAGCATGTG AAATTCCCAAACTCAAAGGATCGTCCTGCCTCCGCCACCTAAAGTGCTGGGATTACAAGCATGTG A C RF00017-1068 RNACentral:URS0000915CF4 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs376792297 Functional Loss SNV dbSNP153 33..33 33 - - - 43317 RMVar_ID_43317 Human_SNP_ID_388712920 A-to-I Human chr9 + 6718547 6718547 6718547 GGGGGATTGCTTGAGCCCAAGAGGTTGAGGCTACATGAGCCATCATCGTGCCACTGCACTCCAGC GGGGGATTGCTTGAGCCCAAGAGGTTGAGGCTCCATGAGCCATCATCGTGCCACTGCACTCCAGC A C AL354707.1 Ensembl:ENSG00000225489 lincRNA exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1021909601 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_301378,RMVar_hsa_circ_70007 43318 RMVar_ID_43318 Human_SNP_ID_388712921 A-to-I Human chr9 + 6718547 6718547 6718547 GGGGGATTGCTTGAGCCCAAGAGGTTGAGGCTACATGAGCCATCATCGTGCCACTGCACTCCAGC GGGGGATTGCTTGAGCCCAAGAGGTTGAGGCTGCATGAGCCATCATCGTGCCACTGCACTCCAGC A G AL354707.1 Ensembl:ENSG00000225489 lincRNA exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1021909601 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_301378,RMVar_hsa_circ_70007 43319 RMVar_ID_43319 Human_SNP_ID_388713394 A-to-I Human chr9 + 6719828 6719828 6719828 GAACTCCTGATCTCAGGTGATCTGCCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAG GAACTCCTGATCTCAGGTGATCTGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAG A G AL354707.1 Ensembl:ENSG00000225489 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs995936766 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_301378,RMVar_hsa_circ_356412 43320 RMVar_ID_43320 Human_SNP_ID_388713402 A-to-I Human chr9 + 6719850 6719850 6719850 TGCCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGCACCTGGCCCCTTTTT TGCCCACCTCAGCCTCCCAAAGTGCTGGGATTGCAGGCATGAGCCACTGCACCTGGCCCCTTTTT A G AL354707.1 Ensembl:ENSG00000225489 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs903706908 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_301378,RMVar_hsa_circ_356412 43321 RMVar_ID_43321 Human_SNP_ID_388713565 A-to-I Human chr9 + 6720220 6720220 6720220 GGGATTACAGCCGTTTGCCACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCA GGGATTACAGCCGTTTGCCACCACGCCCAGCTCATTTTTGTATTTTTAGTAGAGACGGGGTTTCA A C AL354707.1 Ensembl:ENSG00000225489 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs968324807 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_301378,RMVar_hsa_circ_356412 43322 RMVar_ID_43322 Human_SNP_ID_388713566 A-to-I Human chr9 + 6720235 6720235 6720235 TGCCACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGCTGGCCAGGA TGCCACCACGCCCAGCTAATTTTTGTATTTTTGGTAGAGACGGGGTTTCACCATGCTGGCCAGGA A G AL354707.1 Ensembl:ENSG00000225489 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs979687546 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_301378,RMVar_hsa_circ_356412 43323 RMVar_ID_43323 Human_SNP_ID_388713884 A-to-I Human chr9 + 6721137 6721137 6721137 TCTCTGTTGCCCAGGCTAGAGGGCAGTGGTGCAATCACACCTCACTGCAGCCTCAACATCCCAGG TCTCTGTTGCCCAGGCTAGAGGGCAGTGGTGCTATCACACCTCACTGCAGCCTCAACATCCCAGG A T AL354707.1,KDM4C Ensembl:ENSG00000225489,Ensembl:ENSG00000107077 lincRNA,Protein coding exon,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1186785516 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1030618,Human_Splice_Rec_1030619 Human_miRNA_ID_3150403,Human_miRNA_ID_3165865,Human_miRNA_ID_3173455,Human_miRNA_ID_3178918,Human_miRNA_ID_3179271,Human_miRNA_ID_3212051,Human_miRNA_ID_3215594,Human_miRNA_ID_3215688 43324 RMVar_ID_43324 Human_SNP_ID_388714596 A-to-I Human chr9 + 6722908 6722908 6722908 GGAAGGCTGAGGTGGGAGGATTGCGTGAGCCCAGGAGGTTGAGGTTGCAGTGAGTCGAAATCGCA GGAAGGCTGAGGTGGGAGGATTGCGTGAGCCCGGGAGGTTGAGGTTGCAGTGAGTCGAAATCGCA A G AL354707.1,KDM4C Ensembl:ENSG00000225489,Ensembl:ENSG00000107077 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs984730437 Functional Loss SNV dbSNP153 33..33 33 - - - 43325 RMVar_ID_43325 Human_SNP_ID_388735017 A-to-I Human chr9 + 6778498 6778498 6778498 GTTTATCAGATTTTTCCAAGGCCCGGTGCGGTAGCTCACGCCTGTAATCCCAGCACTTTGGGAGG GTTTATCAGATTTTTCCAAGGCCCGGTGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGG A G KDM4C Ensembl:ENSG00000107077 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1191196864 Functional Loss SNV dbSNP153 33..33 33 - - - 43326 RMVar_ID_43326 Human_SNP_ID_388747129 A-to-I Human chr9 + 6810622 6810620 6810623 CGCTGGGTACAGTGGTTCACGCTTGTAGTCCCAACACTTTGGGAGGCTGAGGTTGGAGAATTGCT CGCTGGGTACAGTGGTTCACGCTTGTAGTCC___CACTTTGGGAGGCTGAGGTTGGAGAATTGCT CCAA C KDM4C Ensembl:ENSG00000107077 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1465767068 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_333542,RMVar_hsa_circ_356958,RMVar_hsa_circ_375675,RMVar_hsa_circ_334075,RMVar_hsa_circ_310824,RMVar_hsa_circ_61292,RMVar_hsa_circ_255581,RMVar_hsa_circ_255582,RMVar_hsa_circ_330399,RMVar_hsa_circ_255580 43327 RMVar_ID_43327 Human_SNP_ID_388747383 A-to-I Human chr9 + 6811290 6811290 6811290 ATTCTCCTGCCTCAGCCTCCCGAGCAGCTGGGACCACAGGTGCGTGCCACCATGCCTGGCTAAGT ATTCTCCTGCCTCAGCCTCCCGAGCAGCTGGGGCCACAGGTGCGTGCCACCATGCCTGGCTAAGT A G KDM4C Ensembl:ENSG00000107077 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1237307827 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_333542,RMVar_hsa_circ_356958,RMVar_hsa_circ_375675,RMVar_hsa_circ_334075,RMVar_hsa_circ_310824,RMVar_hsa_circ_61292,RMVar_hsa_circ_255581,RMVar_hsa_circ_255582,RMVar_hsa_circ_330399,RMVar_hsa_circ_255580 43328 RMVar_ID_43328 Human_SNP_ID_388755999 A-to-I Human chr9 + 6835381 6835381 6835381 CTGGCGGCACCACCATGTACCCTAGCGTTGCCAACAGGATGCAGAAGGAGATCACCGCCCTGGCG CTGGCGGCACCACCATGTACCCTAGCGTTGCCGACAGGATGCAGAAGGAGATCACCGCCCTGGCG A G KDM4C,ACTG1P14 Ensembl:ENSG00000107077,Ensembl:ENSG00000230581 Protein coding,Pseudogene intron,exon GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs964239382 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1833988 RMVar_hsa_circ_333542,RMVar_hsa_circ_375675,RMVar_hsa_circ_334075,RMVar_hsa_circ_310824,RMVar_hsa_circ_61292,RMVar_hsa_circ_255581,RMVar_hsa_circ_255580,RMVar_hsa_circ_255585,RMVar_hsa_circ_308349,RMVar_hsa_circ_323138,RMVar_hsa_circ_355806,RMVar_hsa_circ_255586,RMVar_hsa_circ_255587 43329 RMVar_ID_43329 Human_SNP_ID_388756215 A-to-I Human chr9 - 6836025 6836025 6836025 TGGGGGACAAAAGAGGGGGGCCACGAAGGCTGATCATTCAAAATAAAACAAACTTAAAAAGTATT TGGGGGACAAAAGAGGGGGGCCACGAAGGCTGTTCATTCAAAATAAAACAAACTTAAAAAGTATT T A - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1425019239 Functional Loss SNV dbSNP153 33..33 33 - - - 43330 RMVar_ID_43330 Human_SNP_ID_388761446 A-to-I Human chr9 + 6851240 6851240 6851240 GGCTCAAGTGATCCTGCTGCCTCAACCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACTGCAC GGCTCAAGTGATCCTGCTGCCTCAACCTCCCACAGTGCTGGGATTACAGGTGTGAGCCACTGCAC A C KDM4C Ensembl:ENSG00000107077 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904799043 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_375675,RMVar_hsa_circ_334075,RMVar_hsa_circ_310824,RMVar_hsa_circ_61292,RMVar_hsa_circ_255580,RMVar_hsa_circ_308349,RMVar_hsa_circ_355806,RMVar_hsa_circ_255586,RMVar_hsa_circ_255588,RMVar_hsa_circ_255587,RMVar_hsa_circ_321987,RMVar_hsa_circ_332760,RMVar_hsa_circ_286223,RMVar_hsa_circ_7778,RMVar_hsa_circ_73687,RMVar_hsa_circ_89819,RMVar_hsa_circ_9306,RMVar_hsa_circ_255590,RMVar_hsa_circ_255592,RMVar_hsa_circ_255593,RMVar_hsa_circ_255591,RMVar_hsa_circ_255589 43331 RMVar_ID_43331 Human_SNP_ID_388789207 A-to-I Human chr9 + 6934033 6934033 6934033 CACCAAGCCTGGCTAATTTTTGTACTTTTTGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGG CACCAAGCCTGGCTAATTTTTGTACTTTTTGTGGAGATGGGGTTTCACCATGTTGGCCAGGCTGG A G AL513412.1,KDM4C Ensembl:ENSG00000224972,Ensembl:ENSG00000107077 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1418118960 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_375675,RMVar_hsa_circ_310824,RMVar_hsa_circ_61292,RMVar_hsa_circ_255580,RMVar_hsa_circ_355806,RMVar_hsa_circ_321987,RMVar_hsa_circ_127240,RMVar_hsa_circ_7778,RMVar_hsa_circ_73687,RMVar_hsa_circ_89819,RMVar_hsa_circ_9306,RMVar_hsa_circ_255590,RMVar_hsa_circ_255591,RMVar_hsa_circ_255589,RMVar_hsa_circ_321403,RMVar_hsa_circ_96085,RMVar_hsa_circ_47882,RMVar_hsa_circ_77372,RMVar_hsa_circ_255596,RMVar_hsa_circ_255597,RMVar_hsa_circ_255599,RMVar_hsa_circ_3439 43332 RMVar_ID_43332 Human_SNP_ID_388848261 A-to-I Human chr9 + 7109852 7109852 7109852 CTGTGTCCCCACCCAAAATCTCATCTTGAATTATAACCCCCATGTGTCAAGGGCAGTCCAGGTAG CTGTGTCCCCACCCAAAATCTCATCTTGAATTGTAACCCCCATGTGTCAAGGGCAGTCCAGGTAG A G KDM4C Ensembl:ENSG00000107077 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs530411677 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3439,RMVar_hsa_circ_269203,RMVar_hsa_circ_50926,RMVar_hsa_circ_19088,RMVar_hsa_circ_366705,RMVar_hsa_circ_123615,RMVar_hsa_circ_255611,RMVar_hsa_circ_360280,RMVar_hsa_circ_255613,RMVar_hsa_circ_99594,RMVar_hsa_circ_51926,RMVar_hsa_circ_255616,RMVar_hsa_circ_288653,RMVar_hsa_circ_38171,RMVar_hsa_circ_284086,RMVar_hsa_circ_255619,RMVar_hsa_circ_255622,RMVar_hsa_circ_277994 43333 RMVar_ID_43333 Human_SNP_ID_389301414 A-to-I Human chr9 - 8481840 8481840 8481840 AGGTGGAGATTACAGTGAGTCAAGATTGTGCCACTGCACTTCAGCCTGAGCAACAGAGGTATACT AGGTGGAGATTACAGTGAGTCAAGATTGTGCCGCTGCACTTCAGCCTGAGCAACAGAGGTATACT T C PTPRD Ensembl:ENSG00000153707 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1172152716 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127498,RMVar_hsa_circ_255629,RMVar_hsa_circ_4829,RMVar_hsa_circ_16301,RMVar_hsa_circ_45901,RMVar_hsa_circ_45169,RMVar_hsa_circ_31989,RMVar_hsa_circ_318064,RMVar_hsa_circ_19306,RMVar_hsa_circ_26324,RMVar_hsa_circ_47549,RMVar_hsa_circ_304855,RMVar_hsa_circ_345529,RMVar_hsa_circ_255644,RMVar_hsa_circ_255645,RMVar_hsa_circ_35862,RMVar_hsa_circ_309952,RMVar_hsa_circ_324512,RMVar_hsa_circ_327023,RMVar_hsa_circ_310070,RMVar_hsa_circ_304413,RMVar_hsa_circ_267943,RMVar_hsa_circ_269432,RMVar_hsa_circ_49155,RMVar_hsa_circ_31269,RMVar_hsa_circ_33532,RMVar_hsa_circ_6936,RMVar_hsa_circ_51771,RMVar_hsa_circ_255649,RMVar_hsa_circ_255651,RMVar_hsa_circ_255650,RMVar_hsa_circ_342497,RMVar_hsa_circ_255647,RMVar_hsa_circ_255648,RMVar_hsa_circ_255646,RMVar_hsa_circ_378381,RMVar_hsa_circ_292019,RMVar_hsa_circ_333541,RMVar_hsa_circ_268200,RMVar_hsa_circ_48373,RMVar_hsa_circ_36508,RMVar_hsa_circ_255657,RMVar_hsa_circ_35677,RMVar_hsa_circ_348451,RMVar_hsa_circ_255656,RMVar_hsa_circ_282491,RMVar_hsa_circ_255659,RMVar_hsa_circ_35671,RMVar_hsa_circ_255660,RMVar_hsa_circ_328844,RMVar_hsa_circ_255658,RMVar_hsa_circ_331473,RMVar_hsa_circ_306742,RMVar_hsa_circ_255664,RMVar_hsa_circ_255661,RMVar_hsa_circ_255662,RMVar_hsa_circ_111835,RMVar_hsa_circ_321523 43334 RMVar_ID_43334 Human_SNP_ID_389340251 A-to-I Human chr9 - 8594734 8594734 8594734 TTCTTCATGGCTGGGGAGGTCCCAGGAAACTTAGAATCATGGCAGAAAGGGAAGCAGGCACGTTT TTCTTCATGGCTGGGGAGGTCCCAGGAAACTTTGAATCATGGCAGAAAGGGAAGCAGGCACGTTT T A PTPRD Ensembl:ENSG00000153707 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1041523736 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_31269,RMVar_hsa_circ_93621,RMVar_hsa_circ_255671,RMVar_hsa_circ_41058,RMVar_hsa_circ_125293,RMVar_hsa_circ_255678,RMVar_hsa_circ_325145,RMVar_hsa_circ_30632,RMVar_hsa_circ_31531 43335 RMVar_ID_43335 Human_SNP_ID_389418886 A-to-I Human chr9 - 8819063 8819063 8819063 ATGTTTTTAATTTTGAAAGTTGATCTCTTGTTAAACCATCATTTTCTAGCATTTTATGCCTTTTT ATGTTTTTAATTTTGAAAGTTGATCTCTTGTTTAACCATCATTTTCTAGCATTTTATGCCTTTTT T A PTPRD Ensembl:ENSG00000153707 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs925865947 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93621,RMVar_hsa_circ_255671,RMVar_hsa_circ_782,RMVar_hsa_circ_41058,RMVar_hsa_circ_30632,RMVar_hsa_circ_337868,RMVar_hsa_circ_6059,RMVar_hsa_circ_39742 43336 RMVar_ID_43336 Human_SNP_ID_389418891 A-to-I Human chr9 - 8819078 8819078 8819078 TAAGGATACATTTTTATGTTTTTAATTTTGAAAGTTGATCTCTTGTTAAACCATCATTTTCTAGC TAAGGATACATTTTTATGTTTTTAATTTTGAAGGTTGATCTCTTGTTAAACCATCATTTTCTAGC T C PTPRD Ensembl:ENSG00000153707 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1280322486 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93621,RMVar_hsa_circ_255671,RMVar_hsa_circ_782,RMVar_hsa_circ_41058,RMVar_hsa_circ_30632,RMVar_hsa_circ_337868,RMVar_hsa_circ_6059,RMVar_hsa_circ_39742 43337 RMVar_ID_43337 Human_SNP_ID_389581236 A-to-I Human chr9 - 9306635 9306635 9306635 ATGACCCTAAAAATGTGTGCCTTCATTTTCTCAAGTATATTCAGAGGATATTATTGATGATTTTA ATGACCCTAAAAATGTGTGCCTTCATTTTCTCGAGTATATTCAGAGGATATTATTGATGATTTTA T C PTPRD Ensembl:ENSG00000153707 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1371961250 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93621,RMVar_hsa_circ_255671,RMVar_hsa_circ_40598,RMVar_hsa_circ_782,RMVar_hsa_circ_41058,RMVar_hsa_circ_6059,RMVar_hsa_circ_39742 43338 RMVar_ID_43338 Human_SNP_ID_389581237 A-to-I Human chr9 - 9306635 9306635 9306635 ATGACCCTAAAAATGTGTGCCTTCATTTTCTCAAGTATATTCAGAGGATATTATTGATGATTTTA ATGACCCTAAAAATGTGTGCCTTCATTTTCTCCAGTATATTCAGAGGATATTATTGATGATTTTA T G PTPRD Ensembl:ENSG00000153707 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1371961250 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93621,RMVar_hsa_circ_255671,RMVar_hsa_circ_40598,RMVar_hsa_circ_782,RMVar_hsa_circ_41058,RMVar_hsa_circ_6059,RMVar_hsa_circ_39742 43339 RMVar_ID_43339 Human_SNP_ID_389593741 A-to-I Human chr9 - 9343012 9343012 9343012 GGACATGGATGAAGCTGGAAACTATTATTCTCAGCAAACTAACACAGGAACAGAAAACCAAACAC GGACATGGATGAAGCTGGAAACTATTATTCTCGGCAAACTAACACAGGAACAGAAAACCAAACAC T C PTPRD Ensembl:ENSG00000153707 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1045448071 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93621,RMVar_hsa_circ_255671,RMVar_hsa_circ_40598,RMVar_hsa_circ_782,RMVar_hsa_circ_41058,RMVar_hsa_circ_6059,RMVar_hsa_circ_39742 43340 RMVar_ID_43340 Human_SNP_ID_389593745 A-to-I Human chr9 - 9343024 9343024 9343024 TGTCCTTTGCAGGGACATGGATGAAGCTGGAAACTATTATTCTCAGCAAACTAACACAGGAACAG TGTCCTTTGCAGGGACATGGATGAAGCTGGAAGCTATTATTCTCAGCAAACTAACACAGGAACAG T C PTPRD Ensembl:ENSG00000153707 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1470303780 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93621,RMVar_hsa_circ_255671,RMVar_hsa_circ_40598,RMVar_hsa_circ_782,RMVar_hsa_circ_41058,RMVar_hsa_circ_6059,RMVar_hsa_circ_39742 43341 RMVar_ID_43341 Human_SNP_ID_389628627 A-to-I Human chr9 - 9442176 9442176 9442176 TCCCGGGAGGTCACCATATTGATGCCGAACTTAGTGCGGACACCCGATCGGCATAGCGCACTACA TCCCGGGAGGTCACCATATTGATGCCGAACTTCGTGCGGACACCCGATCGGCATAGCGCACTACA T G PTPRD Ensembl:ENSG00000153707 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1247901724 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93621,RMVar_hsa_circ_255671,RMVar_hsa_circ_782,RMVar_hsa_circ_41058,RMVar_hsa_circ_6059,RMVar_hsa_circ_39742 43342 RMVar_ID_43342 Human_SNP_ID_389978930 A-to-I Human chr9 - 10459164 10459164 10459164 CTAGGAACCATCATTCTCAGCAAACTGGCACAAGGACAGAGAACCGAACACCAGATGTTCTTACT CTAGGAACCATCATTCTCAGCAAACTGGCACAGGGACAGAGAACCGAACACCAGATGTTCTTACT T C PTPRD Ensembl:ENSG00000153707 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1480572652 Functional Loss SNV dbSNP153 33..33 33 - - - 43343 RMVar_ID_43343 Human_SNP_ID_389978957 A-to-I Human chr9 - 10459229 10459229 10459229 CCATGGAATATTATGCAGCCATAAAAAAGGATAAGTTCATGTCTTTTGCAGGGACATGGATGAAG CCATGGAATATTATGCAGCCATAAAAAAGGATGAGTTCATGTCTTTTGCAGGGACATGGATGAAG T C PTPRD Ensembl:ENSG00000153707 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1348220033 Functional Loss SNV dbSNP153 33..33 33 - - - 43344 RMVar_ID_43344 Human_SNP_ID_389987979 A-to-I Human chr9 - 10483734 10483734 10483734 GACTTTTTAATAATGGCCATGCTGGCTACAGTAAGGTGATATCTCATTGCAGTTTTAATTTGTAA GACTTTTTAATAATGGCCATGCTGGCTACAGTTAGGTGATATCTCATTGCAGTTTTAATTTGTAA T A PTPRD Ensembl:ENSG00000153707 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1330981391 Functional Loss SNV dbSNP153 33..33 33 - - - 43345 RMVar_ID_43345 Human_SNP_ID_390021267 A-to-I Human chr9 - 10579430 10579429 10579430 GCCATAAAAAAGAACAAAATCATGTTCTTTGCAGCAACATGGGTGCAGCTGGAGGCCACTGTCCT GCCATAAAAAAGAACAAAATCATGTTCTTTGC_GCAACATGGGTGCAGCTGGAGGCCACTGTCCT CT C PTPRD Ensembl:ENSG00000153707 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1202601838 Functional Loss DEL dbSNP153 33..33 33 - - - 43346 RMVar_ID_43346 Human_SNP_ID_390177949 A-to-I Human chr9 - 11053271 11053271 11053271 GACATATACTGAACTCTTTCACTACATTTCCCAGAGTTGTACAATACGTGTTTGTTTAATAAGAG GACATATACTGAACTCTTTCACTACATTTCCCTGAGTTGTACAATACGTGTTTGTTTAATAAGAG T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1413373 Functional Loss SNV dbSNP153 33..33 33 - - - 43347 RMVar_ID_43347 Human_SNP_ID_390177950 A-to-I Human chr9 - 11053271 11053271 11053271 GACATATACTGAACTCTTTCACTACATTTCCCAGAGTTGTACAATACGTGTTTGTTTAATAAGAG GACATATACTGAACTCTTTCACTACATTTCCCGGAGTTGTACAATACGTGTTTGTTTAATAAGAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1413373 Functional Loss SNV dbSNP153 33..33 33 - - - 43348 RMVar_ID_43348 Human_SNP_ID_390592007 A-to-I Human chr9 + 12279766 12279766 12279766 GGGCGTGGTGGCGGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCGGGAGAATGGTGCGAA GGGCGTGGTGGCGGGCGCCTGTAGTCCCAGCTCCTCGGGAGGCTGAGGCGGGAGAATGGTGCGAA A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1305167717 Functional Loss SNV dbSNP153 33..33 33 - - - 43349 RMVar_ID_43349 Human_SNP_ID_390756301 A-to-I Human chr9 - 12804542 12804542 12804542 GGTCAGGAATTCGAGACCAGCCTGGCCAACATAGTGAAACTCCATTTCGACTAAAAACACAAAAA GGTCAGGAATTCGAGACCAGCCTGGCCAACATGGTGAAACTCCATTTCGACTAAAAACACAAAAA T C LURAP1L-AS1 Ensembl:ENSG00000235448 lincRNA intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs915818582 Functional Loss SNV dbSNP153 33..33 33 - - - 43350 RMVar_ID_43350 Human_SNP_ID_390860844 A-to-I Human chr9 - 13140309 13140309 13140309 TATATATATATATGAGCTTTCCATTATTTGTTAGATATTTTATATATATATTATATACATATATG TATATATATATATGAGCTTTCCATTATTTGTTTGATATTTTATATATATATTATATACATATATG T A MPDZ Ensembl:ENSG00000107186 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1449915276 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74184,RMVar_hsa_circ_67980,RMVar_hsa_circ_267695,RMVar_hsa_circ_374079,RMVar_hsa_circ_265123,RMVar_hsa_circ_255734,RMVar_hsa_circ_68240,RMVar_hsa_circ_267359,RMVar_hsa_circ_255735,RMVar_hsa_circ_365119,RMVar_hsa_circ_323237,RMVar_hsa_circ_338294,RMVar_hsa_circ_54658,RMVar_hsa_circ_61068,RMVar_hsa_circ_70666,RMVar_hsa_circ_255736,RMVar_hsa_circ_62695,RMVar_hsa_circ_53770 43351 RMVar_ID_43351 Human_SNP_ID_390885467 A-to-I Human chr9 - 13223699 13223699 13223699 CTTGCTTTGTTTCCTAAACAGGGTCGCCATGTAGAAGTTTTTGAGCTCCTCAAACCTCCATCTGG CTTGCTTTGTTTCCTAAACAGGGTCGCCATGTGGAAGTTTTTGAGCTCCTCAAACCTCCATCTGG T C MPDZ Ensembl:ENSG00000107186 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1255260282 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1031742,Human_Splice_Rec_1031846,Human_Splice_Rec_1031936,Human_Splice_Rec_1032248,Human_Splice_Rec_1032334,Human_Splice_Rec_1032462 RMVar_hsa_circ_67980,RMVar_hsa_circ_15386,RMVar_hsa_circ_362462,RMVar_hsa_circ_276358,RMVar_hsa_circ_15210,RMVar_hsa_circ_17152,RMVar_hsa_circ_18535,RMVar_hsa_circ_255738,RMVar_hsa_circ_16899,RMVar_hsa_circ_255741,RMVar_hsa_circ_255748,RMVar_hsa_circ_255743,RMVar_hsa_circ_348259,RMVar_hsa_circ_255744,RMVar_hsa_circ_364911,RMVar_hsa_circ_299870,RMVar_hsa_circ_255749,RMVar_hsa_circ_255753,RMVar_hsa_circ_255747,RMVar_hsa_circ_282978,RMVar_hsa_circ_313091,RMVar_hsa_circ_339668,RMVar_hsa_circ_11794,RMVar_hsa_circ_255751,RMVar_hsa_circ_255752,RMVar_hsa_circ_255750,RMVar_hsa_circ_364958 43352 RMVar_ID_43352 Human_SNP_ID_391241230 A-to-I Human chr9 - 14375601 14375601 14375601 CAGGCTAGAGTGCAGTGGTGCAATCTCAGCTCACTGCAACCTCCACCTTCCGGTTTCAAGCGATT CAGGCTAGAGTGCAGTGGTGCAATCTCAGCTCGCTGCAACCTCCACCTTCCGGTTTCAAGCGATT T C NFIB Ensembl:ENSG00000147862 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs972980142 Functional Loss SNV dbSNP153 33..33 33 - - - 43353 RMVar_ID_43353 Human_SNP_ID_391241234 A-to-I Human chr9 - 14375606 14375606 14375606 TTGCCCAGGCTAGAGTGCAGTGGTGCAATCTCAGCTCACTGCAACCTCCACCTTCCGGTTTCAAG TTGCCCAGGCTAGAGTGCAGTGGTGCAATCTCGGCTCACTGCAACCTCCACCTTCCGGTTTCAAG T C NFIB Ensembl:ENSG00000147862 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1253823658 Functional Loss SNV dbSNP153 33..33 33 - - - 43354 RMVar_ID_43354 Human_SNP_ID_391241236 A-to-I Human chr9 - 14375611 14375611 14375611 TCTTTTTGCCCAGGCTAGAGTGCAGTGGTGCAATCTCAGCTCACTGCAACCTCCACCTTCCGGTT TCTTTTTGCCCAGGCTAGAGTGCAGTGGTGCACTCTCAGCTCACTGCAACCTCCACCTTCCGGTT T G NFIB Ensembl:ENSG00000147862 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1461507250 Functional Loss SNV dbSNP153 33..33 33 - - - 43355 RMVar_ID_43355 Human_SNP_ID_391411122 A-to-I Human chr9 + 14922360 14922360 14922360 TTGCCACATTGGACTTGGAACCAAAAGGAATCAGGAATGCACATCAGGCAGTCGTCGGGGCGTGT TTGCCACATTGGACTTGGAACCAAAAGGAATCGGGAATGCACATCAGGCAGTCGTCGGGGCGTGT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs565248530 Functional Loss SNV dbSNP153 33..33 33 - - - 43356 RMVar_ID_43356 Human_SNP_ID_391411125 A-to-I Human chr9 + 14922370 14922370 14922370 GGACTTGGAACCAAAAGGAATCAGGAATGCACATCAGGCAGTCGTCGGGGCGTGTGGCAATGAGA GGACTTGGAACCAAAAGGAATCAGGAATGCACGTCAGGCAGTCGTCGGGGCGTGTGGCAATGAGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs577188131 Functional Loss SNV dbSNP153 33..33 33 - - - 43357 RMVar_ID_43357 Human_SNP_ID_391411126 A-to-I Human chr9 + 14922373 14922373 14922373 CTTGGAACCAAAAGGAATCAGGAATGCACATCAGGCAGTCGTCGGGGCGTGTGGCAATGAGATCT CTTGGAACCAAAAGGAATCAGGAATGCACATCGGGCAGTCGTCGGGGCGTGTGGCAATGAGATCT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs541463295 Functional Loss SNV dbSNP153 33..33 33 - - - 43358 RMVar_ID_43358 Human_SNP_ID_37264305 A-to-I Human chr1 - 165663025 165663025 165663025 CTTTTTGAAAACCTGCAGTGAAACCTATTGACATGGCCACGCTGTGGAATGATGTGAATTGGCCC CTTTTTGAAAACCTGCAGTGAAACCTATTGACGTGGCCACGCTGTGGAATGATGTGAATTGGCCC T C ALDH9A1 Ensembl:ENSG00000143149 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs759790607 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_331120,Human_RBP_ID_972385,Human_RBP_ID_4084172,Human_RBP_ID_8288980,Human_RBP_ID_23205416,Human_RBP_ID_23341162 Human_miRNA_ID_215379,Human_miRNA_ID_877063,Human_miRNA_ID_2392191,Human_miRNA_ID_2564437 RMVar_hsa_circ_82595,RMVar_hsa_circ_87668,RMVar_hsa_circ_137275,RMVar_hsa_circ_137276 43359 RMVar_ID_43359 Human_SNP_ID_37279063 A-to-I Human chr1 - 165722587 165722587 165722587 TCGTAAAATATAATATAAATCTGAAGCCGGGCACAGTGGCTCACGCCTGTAATCCCAGCACTTTG TCGTAAAATATAATATAAATCTGAAGCCGGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTTTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1008428424 Functional Loss SNV dbSNP153 33..33 33 - - - 43360 RMVar_ID_43360 Human_SNP_ID_37281132 A-to-I Human chr1 - 165729421 165729421 165729421 TCTCAGCTACTTAGGAGGCTGAGGCAGGCAGAATCGCTTGACCCAGGAGGCAGAGGTTACTGTGA TCTCAGCTACTTAGGAGGCTGAGGCAGGCAGAGTCGCTTGACCCAGGAGGCAGAGGTTACTGTGA T C TMCO1 Ensembl:ENSG00000143183 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1041645643 Functional Loss SNV dbSNP153 33..33 33 - - - 43361 RMVar_ID_43361 Human_SNP_ID_37284845 A-to-I Human chr1 - 165745110 165745107 165745110 AGGCTGAGGCAGGAGGATTCTTTGAGCCCAGGAGGTCAAGGCTGCAGTGAGCCATGATTGCACCA AGGCTGAGGCAGGAGGATTCTTTGAGCCCAGG___TCAAGGCTGCAGTGAGCCATGATTGCACCA ACCT A TMCO1 Ensembl:ENSG00000143183 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1457298341 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_74194,RMVar_hsa_circ_292656,RMVar_hsa_circ_293445,RMVar_hsa_circ_276622,RMVar_hsa_circ_137286,RMVar_hsa_circ_137287 43362 RMVar_ID_43362 Human_SNP_ID_37308591 A-to-I Human chr1 + 165843667 165843667 165843667 AGGTGCAGTGGCATGCACCTGTAGTAGGAGCTACTCAAGAGGCTGAGGTAGGAGGATCTGTGGAG AGGTGCAGTGGCATGCACCTGTAGTAGGAGCTGCTCAAGAGGCTGAGGTAGGAGGATCTGTGGAG A G UCK2 Ensembl:ENSG00000143179 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1312030755 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10632686 43363 RMVar_ID_43363 Human_SNP_ID_37312632 A-to-I Human chr1 + 165860659 165860659 165860659 TTTAGTAGAGACAGAGTTTCAACATGTTGGTCAGGCTGGTCTGGAACTCCTGAGCTCAAGTGATT TTTAGTAGAGACAGAGTTTCAACATGTTGGTCGGGCTGGTCTGGAACTCCTGAGCTCAAGTGATT A G UCK2 Ensembl:ENSG00000143179 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1039777204 Functional Loss SNV dbSNP153 33..33 33 - - - 43364 RMVar_ID_43364 Human_SNP_ID_37324759 A-to-I Human chr1 - 165910910 165910910 165910910 GTACACAAGCCTCCAGCCCGACCCAGCGGCCTAATGAAACTCTGGCAACCTATCCTGGGCGTGGC GTACACAAGCCTCCAGCCCGACCCAGCGGCCTGATGAAACTCTGGCAACCTATCCTGGGCGTGGC T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs982752964 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23121686 43365 RMVar_ID_43365 Human_SNP_ID_37415991 A-to-I Human chr1 + 166276796 166276796 166276796 ATAAACACCCATGCTACTGGGGTGGTCCTGTCAGAATGAACTCTGCTGCCCGTAGCTGCTGCTCT ATAAACACCCATGCTACTGGGGTGGTCCTGTCCGAATGAACTCTGCTGCCCGTAGCTGCTGCTCT A C AL596087.2 Ensembl:ENSG00000229588 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879048038 Functional Loss SNV dbSNP153 33..33 33 - - - 43366 RMVar_ID_43366 Human_SNP_ID_37415992 A-to-I Human chr1 + 166276796 166276796 166276796 ATAAACACCCATGCTACTGGGGTGGTCCTGTCAGAATGAACTCTGCTGCCCGTAGCTGCTGCTCT ATAAACACCCATGCTACTGGGGTGGTCCTGTCGGAATGAACTCTGCTGCCCGTAGCTGCTGCTCT A G AL596087.2 Ensembl:ENSG00000229588 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879048038 Functional Loss SNV dbSNP153 33..33 33 - - - 43367 RMVar_ID_43367 Human_SNP_ID_37416005 A-to-I Human chr1 + 166276832 166276832 166276832 TGAACTCTGCTGCCCGTAGCTGCTGCTCTGTTAGCTATACTGACTTGGAGCTTGGCTGTAGGATC TGAACTCTGCTGCCCGTAGCTGCTGCTCTGTTGGCTATACTGACTTGGAGCTTGGCTGTAGGATC A G AL596087.2 Ensembl:ENSG00000229588 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879166844 Functional Loss SNV dbSNP153 33..33 33 - - - 43368 RMVar_ID_43368 Human_SNP_ID_37416091 A-to-I Human chr1 - 166277177 166277177 166277177 AGCCAGTAGCCACTGCACCTACAAGACTGCAGAATGGAAACAAGCCCACTGAGACTAGTCAACCT AGCCAGTAGCCACTGCACCTACAAGACTGCAGGATGGAAACAAGCCCACTGAGACTAGTCAACCT T C AL596087.1 Ensembl:ENSG00000215835 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879211205 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18524324 43369 RMVar_ID_43369 Human_SNP_ID_37416098 A-to-I Human chr1 + 166277203 166277203 166277203 TTCCATTCTGCAGTCTTGTAGGTGCAGTGGCTACTGGCTGCTGCCCATAAGCTGGATAAGCAGGC TTCCATTCTGCAGTCTTGTAGGTGCAGTGGCTGCTGGCTGCTGCCCATAAGCTGGATAAGCAGGC A G AL596087.2 Ensembl:ENSG00000229588 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878989892 Functional Loss SNV dbSNP153 33..33 33 - - - 43370 RMVar_ID_43370 Human_SNP_ID_37559741 A-to-I Human chr1 + 166856228 166856228 166856228 ATGGTGGTGTGAATCTGTAGTCCCAGCTACTTAGGAGGTTGCGATGGGAGAATCACCTGAGCCCA ATGGTGGTGTGAATCTGTAGTCCCAGCTACTTCGGAGGTTGCGATGGGAGAATCACCTGAGCCCA A C POGK Ensembl:ENSG00000143157 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1248260349 Functional Loss SNV dbSNP153 33..33 33 - - - 43371 RMVar_ID_43371 Human_SNP_ID_37573311 A-to-I Human chr1 - 166913951 166913951 166913951 GCCACCACGTCCAGCAAATTTTGTTTGTTTGTAGAGATGGGGTCTTGCTATATTTCCCAGGCTTG GCCACCACGTCCAGCAAATTTTGTTTGTTTGTGGAGATGGGGTCTTGCTATATTTCCCAGGCTTG T C ILDR2 Ensembl:ENSG00000143195 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1256404413 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23341876 43372 RMVar_ID_43372 Human_SNP_ID_37685025 A-to-I Human chr1 + 167377476 167377464 167377477 AGGCGTGGTGGCAGGCGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATGGTGTGAA AGGCGTGGTGGCAGGCGCCTG_____________TCAGGAGGCTGAGGCAGGAGAATGGTGTGAA GTAGTCCCAGCTAC G POU2F1 Ensembl:ENSG00000143190 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1398721714 Functional Loss DEL dbSNP153 22..34 33 - - - Human_RBP_ID_95392 RMVar_hsa_circ_32153,RMVar_hsa_circ_367912,RMVar_hsa_circ_71056,RMVar_hsa_circ_103017,RMVar_hsa_circ_137328,RMVar_hsa_circ_92690,RMVar_hsa_circ_376827,RMVar_hsa_circ_6997,RMVar_hsa_circ_137330,RMVar_hsa_circ_39905,RMVar_hsa_circ_266191,RMVar_hsa_circ_327357,RMVar_hsa_circ_137332,RMVar_hsa_circ_28962 43373 RMVar_ID_43373 Human_SNP_ID_37685327 A-to-I Human chr1 + 167378606 167378606 167378606 TTTTTGGTTTTTAGTAGAGATGAGGTTTCACTATGTTGGCCAGGCTGGTCTCAAACTCCTGATCT TTTTTGGTTTTTAGTAGAGATGAGGTTTCACTGTGTTGGCCAGGCTGGTCTCAAACTCCTGATCT A G POU2F1 Ensembl:ENSG00000143190 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1007165922 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32153,RMVar_hsa_circ_367912,RMVar_hsa_circ_71056,RMVar_hsa_circ_103017,RMVar_hsa_circ_137328,RMVar_hsa_circ_92690,RMVar_hsa_circ_376827,RMVar_hsa_circ_6997,RMVar_hsa_circ_137330,RMVar_hsa_circ_39905,RMVar_hsa_circ_266191,RMVar_hsa_circ_327357,RMVar_hsa_circ_137332,RMVar_hsa_circ_28962 43374 RMVar_ID_43374 Human_SNP_ID_37688151 A-to-I Human chr1 + 167390516 167390516 167390516 ATTTAAAAACAGTTTTTTGTAGTGGGGGCAGTAGCTCTAATCTGTAATCCCAGCACTTTGGGAGA ATTTAAAAACAGTTTTTTGTAGTGGGGGCAGTGGCTCTAATCTGTAATCCCAGCACTTTGGGAGA A G POU2F1 Ensembl:ENSG00000143190 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1390767180 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22564355 RMVar_hsa_circ_32153,RMVar_hsa_circ_367912,RMVar_hsa_circ_71056,RMVar_hsa_circ_103017,RMVar_hsa_circ_376827,RMVar_hsa_circ_6997,RMVar_hsa_circ_137330,RMVar_hsa_circ_266191,RMVar_hsa_circ_327357,RMVar_hsa_circ_137332,RMVar_hsa_circ_315579,RMVar_hsa_circ_360459,RMVar_hsa_circ_137334,RMVar_hsa_circ_51928,RMVar_hsa_circ_309716,RMVar_hsa_circ_137337 43375 RMVar_ID_43375 Human_SNP_ID_37688444 A-to-I Human chr1 + 167391747 167391747 167391747 CACCACCACACCCGGCTAATTTTTGTAGAGACAAGGTCTTGTCATGTTGCCCAAGCTGGTCTCGA CACCACCACACCCGGCTAATTTTTGTAGAGACGAGGTCTTGTCATGTTGCCCAAGCTGGTCTCGA A G POU2F1 Ensembl:ENSG00000143190 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6672602 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32153,RMVar_hsa_circ_367912,RMVar_hsa_circ_71056,RMVar_hsa_circ_103017,RMVar_hsa_circ_376827,RMVar_hsa_circ_6997,RMVar_hsa_circ_137330,RMVar_hsa_circ_266191,RMVar_hsa_circ_327357,RMVar_hsa_circ_137332,RMVar_hsa_circ_315579,RMVar_hsa_circ_360459,RMVar_hsa_circ_137334,RMVar_hsa_circ_51928,RMVar_hsa_circ_309716,RMVar_hsa_circ_137337 43376 RMVar_ID_43376 Human_SNP_ID_37748850 A-to-I Human chr1 + 167638872 167638872 167638872 TCATTTTAAAGATGACGAAATTGAACATAAGCAATTTACCAATGGTCGTACTTAAAGTCAGTTAG TCATTTTAAAGATGACGAAATTGAACATAAGCGATTTACCAATGGTCGTACTTAAAGTCAGTTAG A G RCSD1 Ensembl:ENSG00000198771 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1229389 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_4991,GWAS_ID_4992,GWAS_ID_4993 43377 RMVar_ID_43377 Human_SNP_ID_37749561 A-to-I Human chr1 + 167641472 167641472 167641472 TGGGTGCAATGGCTCACTCCTGTAATCTCAGCACTTTGGGAGGCCGAGGCAGGTGGATCACAGAA TGGGTGCAATGGCTCACTCCTGTAATCTCAGCGCTTTGGGAGGCCGAGGCAGGTGGATCACAGAA A G RCSD1 Ensembl:ENSG00000198771 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1350258962 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_154440,Human_Splice_Rec_154452 43378 RMVar_ID_43378 Human_SNP_ID_37760161 A-to-I Human chr1 + 167684719 167684719 167684719 CAACATGGAGAAACCCCGTCTCCACTAAAAATACAAAATTGGCCGGGCGTGGTGGCACATGCCTG CAACATGGAGAAACCCCGTCTCCACTAAAAATGCAAAATTGGCCGGGCGTGGTGGCACATGCCTG A G RCSD1 Ensembl:ENSG00000198771 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs542827107 Functional Loss SNV dbSNP153 33..33 33 - - - 43379 RMVar_ID_43379 Human_SNP_ID_37764941 A-to-I Human chr1 + 167702704 167702704 167702704 AGGAGGCTGAGGCAGGAGAATCGCTTGAACCCAGGAGGTGGAGGTTGCAGTGACCTGAGATCGAG AGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGGGAGGTGGAGGTTGCAGTGACCTGAGATCGAG A G RCSD1 Ensembl:ENSG00000198771 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs779354169 Functional Loss SNV dbSNP153 33..33 33 - - - 43380 RMVar_ID_43380 Human_SNP_ID_37772077 A-to-I Human chr1 + 167731516 167731516 167731516 TGGAGTGCAGTGGCGCGATCTCGGCTCACTGCAAGCTTTGCTTCCCAGGTTCATGCCATTCTCCT TGGAGTGCAGTGGCGCGATCTCGGCTCACTGCGAGCTTTGCTTCCCAGGTTCATGCCATTCTCCT A G MPZL1 Ensembl:ENSG00000197965 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs938587242 Functional Loss SNV dbSNP153 33..33 33 - - - 43381 RMVar_ID_43381 Human_SNP_ID_37773913 A-to-I Human chr1 + 167739148 167739144 167739148 GTTTTTTGGTAGAGACAGGGTTTCACCATGTTAGTCAACCTGGTCTTGAGCTCCTGACCTCAGGT GTTTTTTGGTAGAGACAGGGTTTCACCAT____GTCAACCTGGTCTTGAGCTCCTGACCTCAGGT TGTTA T MPZL1 Ensembl:ENSG00000197965 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1422859202 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_10640365 43382 RMVar_ID_43382 Human_SNP_ID_37773920 A-to-I Human chr1 + 167739195 167739195 167739195 GAGCTCCTGACCTCAGGTTATCTGCCTGCCTTAGCCTACCAAAGTGCTGGGATTATAGGTGTGAA GAGCTCCTGACCTCAGGTTATCTGCCTGCCTTGGCCTACCAAAGTGCTGGGATTATAGGTGTGAA A G MPZL1 Ensembl:ENSG00000197965 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054669722 Functional Loss SNV dbSNP153 33..33 33 - - - 43383 RMVar_ID_43383 Human_SNP_ID_37778990 A-to-I Human chr1 + 167760477 167760477 167760477 CGCCCACTTTGGCCTCCCAAAGTGCTGGGATTACAAACGTGAGCCACCGCACCCGGCCCCTCTAG CGCCCACTTTGGCCTCCCAAAGTGCTGGGATTCCAAACGTGAGCCACCGCACCCGGCCCCTCTAG A C MPZL1 Ensembl:ENSG00000197965 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs747855729 Functional Loss SNV dbSNP153 33..33 33 - - - 43384 RMVar_ID_43384 Human_SNP_ID_37788232 A-to-I Human chr1 + 167799402 167799402 167799402 GGGGGGCTGCTTCAGCCCAGGAAGCGGAGGCTATAGTGAGCCGTGATTGTGCCACTGCACTGAAG GGGGGGCTGCTTCAGCCCAGGAAGCGGAGGCTGTAGTGAGCCGTGATTGTGCCACTGCACTGAAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs534853705 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_137350 43385 RMVar_ID_43385 Human_SNP_ID_37831996 A-to-I Human chr1 + 167976348 167976348 167976348 GGAATCAGCTGGGTGTGGTGGTGCACGCCTGTAATACCAGCTACTTGGGAGGCTGAGGCTTGAGA GGAATCAGCTGGGTGTGGTGGTGCACGCCTGTGATACCAGCTACTTGGGAGGCTGAGGCTTGAGA A G DCAF6 Ensembl:ENSG00000143164 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167678786 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10642487 RMVar_hsa_circ_1731,RMVar_hsa_circ_115864,RMVar_hsa_circ_69970,RMVar_hsa_circ_296770,RMVar_hsa_circ_362664,RMVar_hsa_circ_356857,RMVar_hsa_circ_37739,RMVar_hsa_circ_67560,RMVar_hsa_circ_333676,RMVar_hsa_circ_371266,RMVar_hsa_circ_352135,RMVar_hsa_circ_300109,RMVar_hsa_circ_124099,RMVar_hsa_circ_126984,RMVar_hsa_circ_123137,RMVar_hsa_circ_137365,RMVar_hsa_circ_64730,RMVar_hsa_circ_113196,RMVar_hsa_circ_137367,RMVar_hsa_circ_137369,RMVar_hsa_circ_137368,RMVar_hsa_circ_137366,RMVar_hsa_circ_137363,RMVar_hsa_circ_137364,RMVar_hsa_circ_315470,RMVar_hsa_circ_310541,RMVar_hsa_circ_137373 43386 RMVar_ID_43386 Human_SNP_ID_37833239 A-to-I Human chr1 + 167981145 167981145 167981145 CCCAGTCTGGTCTCAGACTCCTGAGCTCAGGTAATCTGCCCGTCTCCGCCTCCAAAGTGCTGGGC CCCAGTCTGGTCTCAGACTCCTGAGCTCAGGTCATCTGCCCGTCTCCGCCTCCAAAGTGCTGGGC A C DCAF6 Ensembl:ENSG00000143164 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1423236829 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1731,RMVar_hsa_circ_115864,RMVar_hsa_circ_69970,RMVar_hsa_circ_296770,RMVar_hsa_circ_362664,RMVar_hsa_circ_356857,RMVar_hsa_circ_37739,RMVar_hsa_circ_67560,RMVar_hsa_circ_333676,RMVar_hsa_circ_371266,RMVar_hsa_circ_352135,RMVar_hsa_circ_300109,RMVar_hsa_circ_124099,RMVar_hsa_circ_126984,RMVar_hsa_circ_123137,RMVar_hsa_circ_137365,RMVar_hsa_circ_64730,RMVar_hsa_circ_113196,RMVar_hsa_circ_137367,RMVar_hsa_circ_137369,RMVar_hsa_circ_137368,RMVar_hsa_circ_137366,RMVar_hsa_circ_137363,RMVar_hsa_circ_137364,RMVar_hsa_circ_315470,RMVar_hsa_circ_310541,RMVar_hsa_circ_137373 43387 RMVar_ID_43387 Human_SNP_ID_37840910 A-to-I Human chr1 + 168011862 168011862 168011862 GTGCGTGGTGGCATGTGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAACTGCATGAA GTGCGTGGTGGCATGTGCCTGTAATCCCAGCTGCTTGGGAGGCTGAGGCAGGAGAACTGCATGAA A G DCAF6 Ensembl:ENSG00000143164 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388903781 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1731,RMVar_hsa_circ_115864,RMVar_hsa_circ_69970,RMVar_hsa_circ_362664,RMVar_hsa_circ_356857,RMVar_hsa_circ_37739,RMVar_hsa_circ_371266,RMVar_hsa_circ_352135,RMVar_hsa_circ_124099,RMVar_hsa_circ_126984,RMVar_hsa_circ_123137,RMVar_hsa_circ_137365,RMVar_hsa_circ_64730,RMVar_hsa_circ_113196,RMVar_hsa_circ_137367,RMVar_hsa_circ_137368,RMVar_hsa_circ_137366,RMVar_hsa_circ_137363,RMVar_hsa_circ_137364,RMVar_hsa_circ_42021,RMVar_hsa_circ_62076,RMVar_hsa_circ_353158,RMVar_hsa_circ_306612,RMVar_hsa_circ_365375,RMVar_hsa_circ_283551,RMVar_hsa_circ_117088,RMVar_hsa_circ_137377,RMVar_hsa_circ_137378,RMVar_hsa_circ_112419,RMVar_hsa_circ_137381 43388 RMVar_ID_43388 Human_SNP_ID_37846151 A-to-I Human chr1 + 168034313 168034313 168034313 GAGGAAGCAGGATCACTTGAGGCCAGGAGTTCAAGACCAGCCTGGACAACATAGTGAGACTCCAT GAGGAAGCAGGATCACTTGAGGCCAGGAGTTCGAGACCAGCCTGGACAACATAGTGAGACTCCAT A G DCAF6 Ensembl:ENSG00000143164 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs948672401 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24604171 RMVar_hsa_circ_1731,RMVar_hsa_circ_362664,RMVar_hsa_circ_37739,RMVar_hsa_circ_371266,RMVar_hsa_circ_352135,RMVar_hsa_circ_124099,RMVar_hsa_circ_126984,RMVar_hsa_circ_123137,RMVar_hsa_circ_137365,RMVar_hsa_circ_64730,RMVar_hsa_circ_113196,RMVar_hsa_circ_137367,RMVar_hsa_circ_137366,RMVar_hsa_circ_137363,RMVar_hsa_circ_137364,RMVar_hsa_circ_62076,RMVar_hsa_circ_306612,RMVar_hsa_circ_365375,RMVar_hsa_circ_36046,RMVar_hsa_circ_366869,RMVar_hsa_circ_305028,RMVar_hsa_circ_358381,RMVar_hsa_circ_50874,RMVar_hsa_circ_31327,RMVar_hsa_circ_137385,RMVar_hsa_circ_350567,RMVar_hsa_circ_359247,RMVar_hsa_circ_273596,RMVar_hsa_circ_137387,RMVar_hsa_circ_11128,RMVar_hsa_circ_137388,RMVar_hsa_circ_137386 43389 RMVar_ID_43389 Human_SNP_ID_37846533 A-to-I Human chr1 + 168035939 168035939 168035939 CAAAAATTAGCCAAGTGTGGTGGTGGGTGCCTATAACCCCAGCTACTCTGGAGGCTGAGGCAGGA CAAAAATTAGCCAAGTGTGGTGGTGGGTGCCTGTAACCCCAGCTACTCTGGAGGCTGAGGCAGGA A G DCAF6 Ensembl:ENSG00000143164 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs572695507 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24604193 RMVar_hsa_circ_1731,RMVar_hsa_circ_362664,RMVar_hsa_circ_37739,RMVar_hsa_circ_371266,RMVar_hsa_circ_352135,RMVar_hsa_circ_124099,RMVar_hsa_circ_126984,RMVar_hsa_circ_123137,RMVar_hsa_circ_137365,RMVar_hsa_circ_64730,RMVar_hsa_circ_113196,RMVar_hsa_circ_137367,RMVar_hsa_circ_137366,RMVar_hsa_circ_137363,RMVar_hsa_circ_137364,RMVar_hsa_circ_62076,RMVar_hsa_circ_306612,RMVar_hsa_circ_365375,RMVar_hsa_circ_36046,RMVar_hsa_circ_366869,RMVar_hsa_circ_305028,RMVar_hsa_circ_358381,RMVar_hsa_circ_50874,RMVar_hsa_circ_31327,RMVar_hsa_circ_137385,RMVar_hsa_circ_350567,RMVar_hsa_circ_359247,RMVar_hsa_circ_273596,RMVar_hsa_circ_137387,RMVar_hsa_circ_11128,RMVar_hsa_circ_137388,RMVar_hsa_circ_137386 43390 RMVar_ID_43390 Human_SNP_ID_37882117 A-to-I Human chr1 + 168181494 168181494 168181494 TCGGCCTCCCAAAGTGCTGGGATTACAGGCATAAGCCACCGCACCCGGCCTCCTCTCCATATAAC TCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCACCCGGCCTCCTCTCCATATAAC A G TIPRL Ensembl:ENSG00000143155 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs899578435 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_137403,RMVar_hsa_circ_83894 43391 RMVar_ID_43391 Human_SNP_ID_37882226 A-to-I Human chr1 + 168181859 168181844 168181860 GAGGCAGGCGGATCACCTGAGGTCAGGAGTTCAAGACCTGCCTGGACAACATGGTGTAACCCCGC GAGGCAGGCGGATCACCT________________GACCTGCCTGGACAACATGGTGTAACCCCGC TGAGGTCAGGAGTTCAA T TIPRL Ensembl:ENSG00000143155 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1468393058 Functional Loss DEL dbSNP153 19..34 33 - - - RMVar_hsa_circ_137403,RMVar_hsa_circ_83894 43392 RMVar_ID_43392 Human_SNP_ID_37882231 A-to-I Human chr1 + 168181859 168181859 168181859 GAGGCAGGCGGATCACCTGAGGTCAGGAGTTCAAGACCTGCCTGGACAACATGGTGTAACCCCGC GAGGCAGGCGGATCACCTGAGGTCAGGAGTTCGAGACCTGCCTGGACAACATGGTGTAACCCCGC A G TIPRL Ensembl:ENSG00000143155 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1475106129 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_137403,RMVar_hsa_circ_83894 43393 RMVar_ID_43393 Human_SNP_ID_37882257 A-to-I Human chr1 + 168181943 168181943 168181943 AAAATTATCTGGGGGTGGTGGTGCAGGCCTGTAATCCCAGCTACTCTGAAGGCTGAGGCACGAGA AAAATTATCTGGGGGTGGTGGTGCAGGCCTGTCATCCCAGCTACTCTGAAGGCTGAGGCACGAGA A C TIPRL Ensembl:ENSG00000143155 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1381128995 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_137403,RMVar_hsa_circ_83894 43394 RMVar_ID_43394 Human_SNP_ID_37897567 A-to-I Human chr1 + 168241402 168241402 168241402 TTTAGTAGAGATGGGGTTTCACCGTGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAAGTGATT TTTAGTAGAGATGGGGTTTCACCGTGTTGGCCGGGCTGGTCTCGAACTCCTGACCTCAAGTGATT A G SFT2D2 Ensembl:ENSG00000213064 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1027799008 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82372,RMVar_hsa_circ_91962,RMVar_hsa_circ_137411,RMVar_hsa_circ_137415,RMVar_hsa_circ_106506,RMVar_hsa_circ_137414,RMVar_hsa_circ_82526,RMVar_hsa_circ_137416,RMVar_hsa_circ_376053,RMVar_hsa_circ_137418,RMVar_hsa_circ_137419,RMVar_hsa_circ_106835,RMVar_hsa_circ_137420,RMVar_hsa_circ_137421 43395 RMVar_ID_43395 Human_SNP_ID_37898290 A-to-I Human chr1 + 168244197 168244197 168244197 CTCTGACTGGTTTTTTTTTTTTTTTCTTTTTGAGATGGAGTCTCACTCCGTCGCCCAGGCTGGAG CTCTGACTGGTTTTTTTTTTTTTTTCTTTTTGTGATGGAGTCTCACTCCGTCGCCCAGGCTGGAG A T SFT2D2 Ensembl:ENSG00000213064 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1385044164 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5709592,Human_RBP_ID_11188142,Human_RBP_ID_19445967,Human_RBP_ID_24395722,Human_RBP_ID_24448193 43396 RMVar_ID_43396 Human_SNP_ID_37898367 A-to-I Human chr1 + 168244453 168244453 168244453 CGCCCACCTTGACCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACTGTGCCCTGCTGATCTTT CGCCCACCTTGACCTCCCAAAGTGCTGGGATTGCAGGTGTGAGCCACTGTGCCCTGCTGATCTTT A G SFT2D2 Ensembl:ENSG00000213064 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1338107624 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4006875,Human_RBP_ID_26371424 Human_miRNA_ID_1079438 43397 RMVar_ID_43397 Human_SNP_ID_37899546 A-to-I Human chr1 + 168249255 168249254 168249255 TAAATTTCCCTCTACACACTGCTTTAATTTTGAAATGGAGTTTTGCTCAGTTTCCCAGGCTAGAG TAAATTTCCCTCTACACACTGCTTTAATTTTG_AATGGAGTTTTGCTCAGTTTCCCAGGCTAGAG GA G SFT2D2 Ensembl:ENSG00000213064 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1327692565 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_10645015,Human_RBP_ID_19220444,Human_RBP_ID_24448239,Human_RBP_ID_26371525 43398 RMVar_ID_43398 Human_SNP_ID_37899567 A-to-I Human chr1 + 168249377 168249377 168249377 TGTGCCTCAGCCTCCCAAGAAACTGGGACTACAGGCATGTGCCACCACACCCGGCTAATTTTTGT TGTGCCTCAGCCTCCCAAGAAACTGGGACTACGGGCATGTGCCACCACACCCGGCTAATTTTTGT A G SFT2D2 Ensembl:ENSG00000213064 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1209115786 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_332280 43399 RMVar_ID_43399 Human_SNP_ID_37899954 A-to-I Human chr1 + 168251042 168251042 168251042 AAATTACCTTTTGGCTGGGTGCAGTGGCTCACACCTGTAATCTGAGCACTTTGGGAGGCTGAGGT AAATTACCTTTTGGCTGGGTGCAGTGGCTCACGCCTGTAATCTGAGCACTTTGGGAGGCTGAGGT A G SFT2D2 Ensembl:ENSG00000213064 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229,31158229 RNA-Seq:(High) rs571019845 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10645109 43400 RMVar_ID_43400 Human_SNP_ID_37899978 A-to-I Human chr1 + 168251133 168251133 168251133 CAAGACCAGCCTGGCCAACATGGCAAAACCCCATCTCTACAAAAAATACAACAGCAAAAAAATCA CAAGACCAGCCTGGCCAACATGGCAAAACCCCGTCTCTACAAAAAATACAACAGCAAAAAAATCA A G SFT2D2 Ensembl:ENSG00000213064 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1249105023 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17730343 43401 RMVar_ID_43401 Human_SNP_ID_37899993 A-to-I Human chr1 + 168251157 168251157 168251157 AAAACCCCATCTCTACAAAAAATACAACAGCAAAAAAATCAGCCAGGCTAGCTGGTGTGCGCCTA AAAACCCCATCTCTACAAAAAATACAACAGCACAAAAATCAGCCAGGCTAGCTGGTGTGCGCCTA A C SFT2D2 Ensembl:ENSG00000213064 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs781752693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23145415 43402 RMVar_ID_43402 Human_SNP_ID_37899999 A-to-I Human chr1 + 168251189 168251189 168251189 AAAAAATCAGCCAGGCTAGCTGGTGTGCGCCTATAATCCCAGCTACTTGGGAGGGAGGCTGAGGC AAAAAATCAGCCAGGCTAGCTGGTGTGCGCCTGTAATCCCAGCTACTTGGGAGGGAGGCTGAGGC A G SFT2D2 Ensembl:ENSG00000213064 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs886830815 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4007029,Human_RBP_ID_24604568 43403 RMVar_ID_43403 Human_SNP_ID_37900009 A-to-I Human chr1 + 168251256 168251256 168251256 AAGAATTGCTTGAACCCAGGAGGTGGAAGTTCAGTGAGCCGAGATCGCACCCCTGCACTCCAGCC AAGAATTGCTTGAACCCAGGAGGTGGAAGTTCGGTGAGCCGAGATCGCACCCCTGCACTCCAGCC A G SFT2D2 Ensembl:ENSG00000213064 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1234979546 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5709704,Human_RBP_ID_10645110 43404 RMVar_ID_43404 Human_SNP_ID_37900019 A-to-I Human chr1 + 168251285 168251285 168251285 TTCAGTGAGCCGAGATCGCACCCCTGCACTCCAGCCTGAGCAACAGAGTGAGACTCTGTCTCAAA TTCAGTGAGCCGAGATCGCACCCCTGCACTCCTGCCTGAGCAACAGAGTGAGACTCTGTCTCAAA A T SFT2D2 Ensembl:ENSG00000213064 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1337258019 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10645110 43405 RMVar_ID_43405 Human_SNP_ID_37900024 A-to-I Human chr1 + 168251297 168251297 168251297 AGATCGCACCCCTGCACTCCAGCCTGAGCAACAGAGTGAGACTCTGTCTCAAAAATAAATAAAAA AGATCGCACCCCTGCACTCCAGCCTGAGCAACGGAGTGAGACTCTGTCTCAAAAATAAATAAAAA A G SFT2D2 Ensembl:ENSG00000213064 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs576923691 Functional Loss SNV dbSNP153 33..33 33 - - - 43406 RMVar_ID_43406 Human_SNP_ID_37900039 A-to-I Human chr1 + 168251329 168251329 168251329 AGAGTGAGACTCTGTCTCAAAAATAAATAAAAAAAAAAATCACTTTTTGATACTTCTGTTAAAAT AGAGTGAGACTCTGTCTCAAAAATAAATAAAATAAAAAATCACTTTTTGATACTTCTGTTAAAAT A T SFT2D2 Ensembl:ENSG00000213064 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1291830372 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17730344 43407 RMVar_ID_43407 Human_SNP_ID_37901264 A-to-I Human chr1 + 168256659 168256659 168256659 TCAGCATTTTGGGAGGCTGAGGTGGGTGGATCACATGAGGCCAGGAGTTCAAGGCCAGCCTGGCC TCAGCATTTTGGGAGGCTGAGGTGGGTGGATCGCATGAGGCCAGGAGTTCAAGGCCAGCCTGGCC A G NONHSAG003392.2 RNACentral:URS00009AFA1D lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1016321564 Functional Loss SNV dbSNP153 33..33 33 - - - 43408 RMVar_ID_43408 Human_SNP_ID_37902691 A-to-I Human chr1 + 168262999 168262999 168262999 ACTCAGCCTCTCGAGTAGCTGGGACTATAGGTATGCACCACTACAAATAGCTAATTTTTCTTTAA ACTCAGCCTCTCGAGTAGCTGGGACTATAGGTGTGCACCACTACAAATAGCTAATTTTTCTTTAA A G NONHSAG003392.2 RNACentral:URS00009AFA1D lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1176440570 Functional Loss SNV dbSNP153 33..33 33 - - - 43409 RMVar_ID_43409 Human_SNP_ID_38115608 A-to-I Human chr1 + 169123654 169123653 169123655 TATCTATATATATAGGTTTTTTTTTTTGAGATAGAGTCTCTGTCACCCAGACTGGAGTGCAGTGG TATCTATATATATAGGTTTTTTTTTTTGAGAT__AGTCTCTGTCACCCAGACTGGAGTGCAGTGG TAG T ATP1B1 Ensembl:ENSG00000143153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1205092987 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_10647359 RMVar_hsa_circ_82070,RMVar_hsa_circ_137425,RMVar_hsa_circ_68623 43410 RMVar_ID_43410 Human_SNP_ID_38196422 A-to-I Human chr1 - 169473270 169473270 169473270 AGATAGTGCCACTGTACTCTAGCCTGGGCAACAGAGACTCTGTCTCAAAAAAATAAATAAATAAA AGATAGTGCCACTGTACTCTAGCCTGGGCAACGGAGACTCTGTCTCAAAAAAATAAATAAATAAA T C SLC19A2 Ensembl:ENSG00000117479 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs974620343 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_284892,RMVar_hsa_circ_137450 43411 RMVar_ID_43411 Human_SNP_ID_38197961 A-to-I Human chr1 - 169480255 169480255 169480255 GGCCACAAAGGAATGACAAGTTGTTAATTAGAACACAACTGGAAATCTCAAGATTACCCTTACCT GGCCACAAAGGAATGACAAGTTGTTAATTAGAGCACAACTGGAAATCTCAAGATTACCCTTACCT T C SLC19A2 Ensembl:ENSG00000117479 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1357793752 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_137452,RMVar_hsa_circ_90746 43412 RMVar_ID_43412 Human_SNP_ID_38197963 A-to-I Human chr1 - 169480258 169480258 169480258 ATAGGCCACAAAGGAATGACAAGTTGTTAATTAGAACACAACTGGAAATCTCAAGATTACCCTTA ATAGGCCACAAAGGAATGACAAGTTGTTAATTGGAACACAACTGGAAATCTCAAGATTACCCTTA T C SLC19A2 Ensembl:ENSG00000117479 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1320178470 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_137452,RMVar_hsa_circ_90746 43413 RMVar_ID_43413 Human_SNP_ID_38198432 A-to-I Human chr1 - 169482348 169482348 169482348 TTTAGTAGAGTCGGGGTTTTGCCATGTTGGCCAGGCTGGTTTTGAACCCCTGGCCTCAAGTGATC TTTAGTAGAGTCGGGGTTTTGCCATGTTGGCCGGGCTGGTTTTGAACCCCTGGCCTCAAGTGATC T C SLC19A2 Ensembl:ENSG00000117479 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1208427662 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_137452,RMVar_hsa_circ_90746 43414 RMVar_ID_43414 Human_SNP_ID_38276025 A-to-I Human chr1 + 169798323 169798323 169798323 TTTGAGACGGAGTCTCGCCTATGCTGGAGTGCAATGGCGCGATCTTGGCTCACTGCAACCTCTGC TTTGAGACGGAGTCTCGCCTATGCTGGAGTGCGATGGCGCGATCTTGGCTCACTGCAACCTCTGC A G C1orf112 Ensembl:ENSG00000000460 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1011254296 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2727,RMVar_hsa_circ_128099,RMVar_hsa_circ_12799,RMVar_hsa_circ_137457 43415 RMVar_ID_43415 Human_SNP_ID_38279388 A-to-I Human chr1 + 169811607 169811607 169811607 AGCCCAGGAGATTGAGGCTGCAGTGAGCCATGATCAGGCCACTGTACTCCAGCTTGGACAACAGA AGCCCAGGAGATTGAGGCTGCAGTGAGCCATGGTCAGGCCACTGTACTCCAGCTTGGACAACAGA A G C1orf112 Ensembl:ENSG00000000460 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1447685200 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5711261 RMVar_hsa_circ_2727,RMVar_hsa_circ_37881,RMVar_hsa_circ_276473,RMVar_hsa_circ_331971,RMVar_hsa_circ_370713,RMVar_hsa_circ_351834,RMVar_hsa_circ_73854,RMVar_hsa_circ_66890,RMVar_hsa_circ_137459,RMVar_hsa_circ_137461,RMVar_hsa_circ_137460,RMVar_hsa_circ_137458,RMVar_hsa_circ_265822,RMVar_hsa_circ_9069,RMVar_hsa_circ_36328,RMVar_hsa_circ_97074,RMVar_hsa_circ_137469,RMVar_hsa_circ_24865,RMVar_hsa_circ_35577,RMVar_hsa_circ_50646,RMVar_hsa_circ_299967,RMVar_hsa_circ_137470 43416 RMVar_ID_43416 Human_SNP_ID_38288691 A-to-I Human chr1 - 169850782 169850778 169850782 GAACTACAAGTGTCCTTTTTTGAGACAGTCTCACTCTGTCGCTCAGGCTGGAGTGCAGTGGCATG GAACTACAAGTGTCCTTTTTTGAGACAGTCTC____TGTCGCTCAGGCTGGAGTGCAGTGGCATG AGAGT A SCYL3 Ensembl:ENSG00000000457 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1184731969 Functional Loss DEL dbSNP153 33..36 33 - - - 43417 RMVar_ID_43417 Human_SNP_ID_38289001 A-to-I Human chr1 - 169851421 169851421 169851421 GGAGGAATGCTTGAGCCCAGGAGTTTGAGGTTATAGCGAGCTATGATCACACCACCACACTCCAA GGAGGAATGCTTGAGCCCAGGAGTTTGAGGTTGTAGCGAGCTATGATCACACCACCACACTCCAA T C SCYL3 Ensembl:ENSG00000000457 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs538241694 Functional Loss SNV dbSNP153 33..33 33 - - - 43418 RMVar_ID_43418 Human_SNP_ID_38333528 A-to-I Human chr1 - 170041459 170041459 170041459 TTTTACATTTTTTGTAGAGACGGGGTCTCACTATGTTGCCTAGGCTAGTCTCAAACTCCTGGGCT TTTTACATTTTTTGTAGAGACGGGGTCTCACTGTGTTGCCTAGGCTAGTCTCAAACTCCTGGGCT T C KIFAP3 Ensembl:ENSG00000075945 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1297473075 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76725,RMVar_hsa_circ_137483,RMVar_hsa_circ_342382,RMVar_hsa_circ_293450,RMVar_hsa_circ_137484,RMVar_hsa_circ_328602,RMVar_hsa_circ_327714,RMVar_hsa_circ_113366,RMVar_hsa_circ_137500,RMVar_hsa_circ_137499,RMVar_hsa_circ_349482,RMVar_hsa_circ_313407,RMVar_hsa_circ_11986,RMVar_hsa_circ_137503,RMVar_hsa_circ_357184,RMVar_hsa_circ_137505,RMVar_hsa_circ_38722,RMVar_hsa_circ_367168 43419 RMVar_ID_43419 Human_SNP_ID_38685271 A-to-I Human chr1 + 171487738 171487738 171487738 TAATGGATAATGTATGTAAAGGGCTTATTACTATGCTTAGTGCATAGTAAAAGGTCAACTAATAG TAATGGATAATGTATGTAAAGGGCTTATTACTGTGCTTAGTGCATAGTAAAAGGTCAACTAATAG A G PRRC2C Ensembl:ENSG00000117523 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1297098491 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557381 RMVar_hsa_circ_137515,RMVar_hsa_circ_107472,RMVar_hsa_circ_116819,RMVar_hsa_circ_137516 43420 RMVar_ID_43420 Human_SNP_ID_38686489 A-to-I Human chr1 + 171492984 171492984 171492984 GTGTTGGCCAGGCTGGTCCTGAACTGACCTCAAATGATCCACCTGCCTCGCCCTCCCAAAGTGCT GTGTTGGCCAGGCTGGTCCTGAACTGACCTCAGATGATCCACCTGCCTCGCCCTCCCAAAGTGCT A G PRRC2C Ensembl:ENSG00000117523 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042699879 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_137515,RMVar_hsa_circ_107472,RMVar_hsa_circ_116819,RMVar_hsa_circ_137516 43421 RMVar_ID_43421 Human_SNP_ID_38687446 A-to-I Human chr1 + 171496881 171496881 171496881 AGAGTGCAGTGGTGCAATCATTGGCTCACTGTAGCCTCAACCTCCCAGGCTCAAGCGATCCTCCT AGAGTGCAGTGGTGCAATCATTGGCTCACTGTGGCCTCAACCTCCCAGGCTCAAGCGATCCTCCT A G PRRC2C Ensembl:ENSG00000117523 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1385778633 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10650955,Human_RBP_ID_23344340 RMVar_hsa_circ_137515,RMVar_hsa_circ_107472,RMVar_hsa_circ_116819,RMVar_hsa_circ_137516 43422 RMVar_ID_43422 Human_SNP_ID_38687448 A-to-I Human chr1 + 171496895 171496895 171496895 CAATCATTGGCTCACTGTAGCCTCAACCTCCCAGGCTCAAGCGATCCTCCTGCTTCAATCTCCTG CAATCATTGGCTCACTGTAGCCTCAACCTCCCGGGCTCAAGCGATCCTCCTGCTTCAATCTCCTG A G PRRC2C Ensembl:ENSG00000117523 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs771082698 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10650956,Human_RBP_ID_23344340 RMVar_hsa_circ_137515,RMVar_hsa_circ_107472,RMVar_hsa_circ_116819,RMVar_hsa_circ_137516 43423 RMVar_ID_43423 Human_SNP_ID_38687474 A-to-I Human chr1 + 171496980 171496980 171496980 CCACCACACCTGGCTATTTTTTTGGTAGAGACAAGGTCTCTCCATGTTGCTCAGGCTGGTCTCAA CCACCACACCTGGCTATTTTTTTGGTAGAGACGAGGTCTCTCCATGTTGCTCAGGCTGGTCTCAA A G PRRC2C Ensembl:ENSG00000117523 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs769559875 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9556237,Human_RBP_ID_11188512,Human_RBP_ID_23344344 RMVar_hsa_circ_137515,RMVar_hsa_circ_107472,RMVar_hsa_circ_116819,RMVar_hsa_circ_137516 43424 RMVar_ID_43424 Human_SNP_ID_38688084 A-to-I Human chr1 + 171499517 171499517 171499517 TTATTAATAGAAAAGGGAGAGATGGGCCGGGCACGGTGGCTCACGCCTGTAATCTCAGCACTTTG TTATTAATAGAAAAGGGAGAGATGGGCCGGGCGCGGTGGCTCACGCCTGTAATCTCAGCACTTTG A G PRRC2C Ensembl:ENSG00000117523 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1174753497 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_137515,RMVar_hsa_circ_107472,RMVar_hsa_circ_116819,RMVar_hsa_circ_137516 43425 RMVar_ID_43425 Human_SNP_ID_38688437 A-to-I Human chr1 + 171501002 171501002 171501002 CTCACTGCAGCCTCGACTTCCTGTGCTCCAGCAGTCCTCCCACCTCAGCCTCCTGAGTAGCTGGG CTCACTGCAGCCTCGACTTCCTGTGCTCCAGCCGTCCTCCCACCTCAGCCTCCTGAGTAGCTGGG A C PRRC2C Ensembl:ENSG00000117523 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs908598632 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10651195 RMVar_hsa_circ_137515,RMVar_hsa_circ_107472,RMVar_hsa_circ_116819,RMVar_hsa_circ_137516 43426 RMVar_ID_43426 Human_SNP_ID_38695286 A-to-I Human chr1 + 171527515 171527515 171527515 GTGGTGGCTCACATCTGTAATCCTAGCACTTTAGGAGGCTAAGGCAGGCAGATCACTTGACATCA GTGGTGGCTCACATCTGTAATCCTAGCACTTTGGGAGGCTAAGGCAGGCAGATCACTTGACATCA A G PRRC2C Ensembl:ENSG00000117523 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1236704378 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3751,RMVar_hsa_circ_24697,RMVar_hsa_circ_353201,RMVar_hsa_circ_326203,RMVar_hsa_circ_34691,RMVar_hsa_circ_7543,RMVar_hsa_circ_137518,RMVar_hsa_circ_62597,RMVar_hsa_circ_373755,RMVar_hsa_circ_137520,RMVar_hsa_circ_29955,RMVar_hsa_circ_127759,RMVar_hsa_circ_119908,RMVar_hsa_circ_137522,RMVar_hsa_circ_102744,RMVar_hsa_circ_137526,RMVar_hsa_circ_137527,RMVar_hsa_circ_367389,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_300929,RMVar_hsa_circ_357105,RMVar_hsa_circ_367400,RMVar_hsa_circ_299901,RMVar_hsa_circ_61651,RMVar_hsa_circ_95335,RMVar_hsa_circ_104861,RMVar_hsa_circ_137535,RMVar_hsa_circ_137537,RMVar_hsa_circ_137538,RMVar_hsa_circ_137536,RMVar_hsa_circ_137534,RMVar_hsa_circ_58235,RMVar_hsa_circ_70761,RMVar_hsa_circ_297569,RMVar_hsa_circ_137539,RMVar_hsa_circ_315663,RMVar_hsa_circ_294152,RMVar_hsa_circ_137540,RMVar_hsa_circ_137541,RMVar_hsa_circ_137542 43427 RMVar_ID_43427 Human_SNP_ID_38695295 A-to-I Human chr1 + 171527570 171527570 171527570 CTTGACATCAGGAGTTCAAGAACAGCCTGGCCAACATGGCAAAACCCTGTCTCTACTAAAAATGC CTTGACATCAGGAGTTCAAGAACAGCCTGGCCGACATGGCAAAACCCTGTCTCTACTAAAAATGC A G PRRC2C Ensembl:ENSG00000117523 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs986449534 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3751,RMVar_hsa_circ_24697,RMVar_hsa_circ_353201,RMVar_hsa_circ_326203,RMVar_hsa_circ_34691,RMVar_hsa_circ_7543,RMVar_hsa_circ_137518,RMVar_hsa_circ_62597,RMVar_hsa_circ_373755,RMVar_hsa_circ_137520,RMVar_hsa_circ_29955,RMVar_hsa_circ_127759,RMVar_hsa_circ_119908,RMVar_hsa_circ_137522,RMVar_hsa_circ_102744,RMVar_hsa_circ_137526,RMVar_hsa_circ_137527,RMVar_hsa_circ_367389,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_300929,RMVar_hsa_circ_357105,RMVar_hsa_circ_367400,RMVar_hsa_circ_299901,RMVar_hsa_circ_61651,RMVar_hsa_circ_95335,RMVar_hsa_circ_104861,RMVar_hsa_circ_137535,RMVar_hsa_circ_137537,RMVar_hsa_circ_137538,RMVar_hsa_circ_137536,RMVar_hsa_circ_137534,RMVar_hsa_circ_58235,RMVar_hsa_circ_70761,RMVar_hsa_circ_297569,RMVar_hsa_circ_137539,RMVar_hsa_circ_315663,RMVar_hsa_circ_294152,RMVar_hsa_circ_137540,RMVar_hsa_circ_137541,RMVar_hsa_circ_137542 43428 RMVar_ID_43428 Human_SNP_ID_38695327 A-to-I Human chr1 + 171527688 171527687 171527689 TGAGGCATGAGAATTGCTTGGCCCCGGGAGACAGAGGTTGCAGTGAGCCAAGATCATGCCACTGC TGAGGCATGAGAATTGCTTGGCCCCGGGAGAC__AGGTTGCAGTGAGCCAAGATCATGCCACTGC CAG C PRRC2C Ensembl:ENSG00000117523 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1557920352 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_22637797 RMVar_hsa_circ_3751,RMVar_hsa_circ_24697,RMVar_hsa_circ_353201,RMVar_hsa_circ_326203,RMVar_hsa_circ_34691,RMVar_hsa_circ_7543,RMVar_hsa_circ_137518,RMVar_hsa_circ_62597,RMVar_hsa_circ_373755,RMVar_hsa_circ_137520,RMVar_hsa_circ_29955,RMVar_hsa_circ_127759,RMVar_hsa_circ_119908,RMVar_hsa_circ_137522,RMVar_hsa_circ_102744,RMVar_hsa_circ_137526,RMVar_hsa_circ_137527,RMVar_hsa_circ_367389,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_300929,RMVar_hsa_circ_357105,RMVar_hsa_circ_367400,RMVar_hsa_circ_299901,RMVar_hsa_circ_61651,RMVar_hsa_circ_95335,RMVar_hsa_circ_104861,RMVar_hsa_circ_137535,RMVar_hsa_circ_137537,RMVar_hsa_circ_137538,RMVar_hsa_circ_137536,RMVar_hsa_circ_137534,RMVar_hsa_circ_58235,RMVar_hsa_circ_70761,RMVar_hsa_circ_297569,RMVar_hsa_circ_137539,RMVar_hsa_circ_315663,RMVar_hsa_circ_294152,RMVar_hsa_circ_137540,RMVar_hsa_circ_137541,RMVar_hsa_circ_137542 43429 RMVar_ID_43429 Human_SNP_ID_38708463 A-to-I Human chr1 + 171577871 171577871 171577871 GCGGTCTTGGCTTACTGCCACCTCCACCTCCCAGGTTCAAGTGATCCTCTCACCTCAGCCTCCCA GCGGTCTTGGCTTACTGCCACCTCCACCTCCCGGGTTCAAGTGATCCTCTCACCTCAGCCTCCCA A G PRRC2C Ensembl:ENSG00000117523 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432761482 Functional Loss SNV dbSNP153 33..33 33 - - - 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_95335,RMVar_hsa_circ_93339,RMVar_hsa_circ_104861,RMVar_hsa_circ_137537,RMVar_hsa_circ_137538,RMVar_hsa_circ_137539,RMVar_hsa_circ_137545,RMVar_hsa_circ_369535,RMVar_hsa_circ_122977,RMVar_hsa_circ_137549,RMVar_hsa_circ_137550,RMVar_hsa_circ_2571,RMVar_hsa_circ_79759,RMVar_hsa_circ_85082,RMVar_hsa_circ_137553,RMVar_hsa_circ_101276,RMVar_hsa_circ_22801,RMVar_hsa_circ_137554,RMVar_hsa_circ_82768,RMVar_hsa_circ_87401,RMVar_hsa_circ_309501,RMVar_hsa_circ_137558,RMVar_hsa_circ_137559,RMVar_hsa_circ_372142,RMVar_hsa_circ_94816,RMVar_hsa_circ_137564,RMVar_hsa_circ_137565,RMVar_hsa_circ_137563,RMVar_hsa_circ_43268,RMVar_hsa_circ_85804,RMVar_hsa_circ_137566,RMVar_hsa_circ_81637,RMVar_hsa_circ_74086,RMVar_hsa_circ_137567 43430 RMVar_ID_43430 Human_SNP_ID_38708606 A-to-I Human chr1 + 171578351 171578351 171578351 AAGGCAGAAGGATTACTTGACCCTAGGAGTTCAAGACCAACCCGAGCAACATAGTGAGACCCATC AAGGCAGAAGGATTACTTGACCCTAGGAGTTCTAGACCAACCCGAGCAACATAGTGAGACCCATC A T PRRC2C Ensembl:ENSG00000117523 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs759087826 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10653281,Human_RBP_ID_17730898,Human_RBP_ID_24754257 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_95335,RMVar_hsa_circ_93339,RMVar_hsa_circ_104861,RMVar_hsa_circ_137537,RMVar_hsa_circ_137538,RMVar_hsa_circ_137539,RMVar_hsa_circ_137545,RMVar_hsa_circ_369535,RMVar_hsa_circ_122977,RMVar_hsa_circ_137549,RMVar_hsa_circ_137550,RMVar_hsa_circ_2571,RMVar_hsa_circ_79759,RMVar_hsa_circ_85082,RMVar_hsa_circ_137553,RMVar_hsa_circ_101276,RMVar_hsa_circ_22801,RMVar_hsa_circ_137554,RMVar_hsa_circ_82768,RMVar_hsa_circ_87401,RMVar_hsa_circ_309501,RMVar_hsa_circ_137558,RMVar_hsa_circ_137559,RMVar_hsa_circ_372142,RMVar_hsa_circ_94816,RMVar_hsa_circ_137564,RMVar_hsa_circ_137565,RMVar_hsa_circ_137563,RMVar_hsa_circ_43268,RMVar_hsa_circ_85804,RMVar_hsa_circ_137566,RMVar_hsa_circ_81637,RMVar_hsa_circ_74086,RMVar_hsa_circ_137567 43431 RMVar_ID_43431 Human_SNP_ID_38708711 A-to-I Human chr1 + 171578753 171578753 171578753 GGTTGGGCGTGGTGGCGCACACTCAGCTGCTCAGGTAGCTGAGGCACAAGAATCGCTTGAACCCG GGTTGGGCGTGGTGGCGCACACTCAGCTGCTCGGGTAGCTGAGGCACAAGAATCGCTTGAACCCG A G PRRC2C Ensembl:ENSG00000117523 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1001548899 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8290289 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_95335,RMVar_hsa_circ_93339,RMVar_hsa_circ_104861,RMVar_hsa_circ_137537,RMVar_hsa_circ_137538,RMVar_hsa_circ_137539,RMVar_hsa_circ_137545,RMVar_hsa_circ_369535,RMVar_hsa_circ_122977,RMVar_hsa_circ_137549,RMVar_hsa_circ_137550,RMVar_hsa_circ_2571,RMVar_hsa_circ_79759,RMVar_hsa_circ_85082,RMVar_hsa_circ_137553,RMVar_hsa_circ_101276,RMVar_hsa_circ_22801,RMVar_hsa_circ_137554,RMVar_hsa_circ_82768,RMVar_hsa_circ_87401,RMVar_hsa_circ_309501,RMVar_hsa_circ_137558,RMVar_hsa_circ_137559,RMVar_hsa_circ_372142,RMVar_hsa_circ_94816,RMVar_hsa_circ_137564,RMVar_hsa_circ_137565,RMVar_hsa_circ_137563,RMVar_hsa_circ_43268,RMVar_hsa_circ_85804,RMVar_hsa_circ_137566,RMVar_hsa_circ_81637,RMVar_hsa_circ_74086,RMVar_hsa_circ_137567 43432 RMVar_ID_43432 Human_SNP_ID_38708712 A-to-I Human chr1 + 171578753 171578753 171578753 GGTTGGGCGTGGTGGCGCACACTCAGCTGCTCAGGTAGCTGAGGCACAAGAATCGCTTGAACCCG GGTTGGGCGTGGTGGCGCACACTCAGCTGCTCTGGTAGCTGAGGCACAAGAATCGCTTGAACCCG A T PRRC2C Ensembl:ENSG00000117523 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1001548899 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8290289 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_95335,RMVar_hsa_circ_93339,RMVar_hsa_circ_104861,RMVar_hsa_circ_137537,RMVar_hsa_circ_137538,RMVar_hsa_circ_137539,RMVar_hsa_circ_137545,RMVar_hsa_circ_369535,RMVar_hsa_circ_122977,RMVar_hsa_circ_137549,RMVar_hsa_circ_137550,RMVar_hsa_circ_2571,RMVar_hsa_circ_79759,RMVar_hsa_circ_85082,RMVar_hsa_circ_137553,RMVar_hsa_circ_101276,RMVar_hsa_circ_22801,RMVar_hsa_circ_137554,RMVar_hsa_circ_82768,RMVar_hsa_circ_87401,RMVar_hsa_circ_309501,RMVar_hsa_circ_137558,RMVar_hsa_circ_137559,RMVar_hsa_circ_372142,RMVar_hsa_circ_94816,RMVar_hsa_circ_137564,RMVar_hsa_circ_137565,RMVar_hsa_circ_137563,RMVar_hsa_circ_43268,RMVar_hsa_circ_85804,RMVar_hsa_circ_137566,RMVar_hsa_circ_81637,RMVar_hsa_circ_74086,RMVar_hsa_circ_137567 43433 RMVar_ID_43433 Human_SNP_ID_38708740 A-to-I Human chr1 + 171578846 171578845 171578846 CAATCGTGCCACTGCACTTCAGCCTGGGTGACAAAGCGAGACTGTTTCAAAACAAAAAACAAAAA CAATCGTGCCACTGCACTTCAGCCTGGGTGAC_AAGCGAGACTGTTTCAAAACAAAAAACAAAAA CA C PRRC2C Ensembl:ENSG00000117523 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1428453619 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_10653295 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_95335,RMVar_hsa_circ_93339,RMVar_hsa_circ_104861,RMVar_hsa_circ_137537,RMVar_hsa_circ_137538,RMVar_hsa_circ_137539,RMVar_hsa_circ_137545,RMVar_hsa_circ_369535,RMVar_hsa_circ_122977,RMVar_hsa_circ_137549,RMVar_hsa_circ_137550,RMVar_hsa_circ_2571,RMVar_hsa_circ_79759,RMVar_hsa_circ_85082,RMVar_hsa_circ_137553,RMVar_hsa_circ_101276,RMVar_hsa_circ_22801,RMVar_hsa_circ_137554,RMVar_hsa_circ_82768,RMVar_hsa_circ_87401,RMVar_hsa_circ_309501,RMVar_hsa_circ_137558,RMVar_hsa_circ_137559,RMVar_hsa_circ_372142,RMVar_hsa_circ_94816,RMVar_hsa_circ_137564,RMVar_hsa_circ_137565,RMVar_hsa_circ_137563,RMVar_hsa_circ_43268,RMVar_hsa_circ_85804,RMVar_hsa_circ_137566,RMVar_hsa_circ_81637,RMVar_hsa_circ_74086,RMVar_hsa_circ_137567 43434 RMVar_ID_43434 Human_SNP_ID_38739370 A-to-I Human chr1 - 171701542 171701542 171701542 TGATAGCAAAAATTGGCATCTTTCAATTCTGTATAGTATGTGACTATCCTGTAAATGATAATATG TGATAGCAAAAATTGGCATCTTTCAATTCTGTGTAGTATGTGACTATCCTGTAAATGATAATATG T C VAMP4 Ensembl:ENSG00000117533 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1397552138 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_332887,Human_RBP_ID_3286684,Human_RBP_ID_23344717 Human_miRNA_ID_671656 RMVar_hsa_circ_265930 43435 RMVar_ID_43435 Human_SNP_ID_38753278 A-to-I Human chr1 + 171762356 171762356 171762356 AGGAGGTGACTTTGGGGCCCATGGGCGTGGTCACAGCTACTCTAGAGGTGGTGGGAACCAGGACT AGGAGGTGACTTTGGGGCCCATGGGCGTGGTCGCAGCTACTCTAGAGGTGGTGGGAACCAGGACT A G Z98751.2 Ensembl:ENSG00000236741 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1189514810 Functional Loss SNV dbSNP153 33..33 33 - - - 43436 RMVar_ID_43436 Human_SNP_ID_38753284 A-to-I Human chr1 + 171762379 171762379 171762379 GGCGTGGTCACAGCTACTCTAGAGGTGGTGGGAACCAGGACTATGGGAGTGGCAGGTATGACAGT GGCGTGGTCACAGCTACTCTAGAGGTGGTGGGGACCAGGACTATGGGAGTGGCAGGTATGACAGT A G Z98751.2 Ensembl:ENSG00000236741 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1463739982 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5890114,Human_RBP_ID_8241454 43437 RMVar_ID_43437 Human_SNP_ID_38753286 A-to-I Human chr1 + 171762386 171762386 171762386 TCACAGCTACTCTAGAGGTGGTGGGAACCAGGACTATGGGAGTGGCAGGTATGACAGTTGACCTG TCACAGCTACTCTAGAGGTGGTGGGAACCAGGGCTATGGGAGTGGCAGGTATGACAGTTGACCTG A G Z98751.2 Ensembl:ENSG00000236741 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1209178334 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5890114,Human_RBP_ID_8241454 43438 RMVar_ID_43438 Human_SNP_ID_38833125 A-to-I Human chr1 + 172110980 172110980 172110980 ATCCCCTGAGCCGGGGAGATCGAGGTTGCAGTAAGCTGAAATTGTGCCAGGGCACTCCAGCCTGA ATCCCCTGAGCCGGGGAGATCGAGGTTGCAGTGAGCTGAAATTGTGCCAGGGCACTCCAGCCTGA A G DNM3 Ensembl:ENSG00000197959 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1174284249 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58,RMVar_hsa_circ_16263,RMVar_hsa_circ_137606,RMVar_hsa_circ_14356,RMVar_hsa_circ_3248,RMVar_hsa_circ_5208,RMVar_hsa_circ_267180,RMVar_hsa_circ_337626,RMVar_hsa_circ_27069,RMVar_hsa_circ_137599,RMVar_hsa_circ_340542,RMVar_hsa_circ_267801,RMVar_hsa_circ_316584,RMVar_hsa_circ_340078,RMVar_hsa_circ_137604,RMVar_hsa_circ_43556,RMVar_hsa_circ_285961,RMVar_hsa_circ_269467,RMVar_hsa_circ_320531,RMVar_hsa_circ_137607 43439 RMVar_ID_43439 Human_SNP_ID_38908620 A-to-I Human chr1 + 172443837 172443837 172443837 TGGGAGGGGACGGGGTAGGGTAGGGTGACCCCAGGGTGCGCCTTCACTCTTCTGGCACCCCATTT TGGGAGGGGACGGGGTAGGGTAGGGTGACCCCGGGGTGCGCCTTCACTCTTCTGGCACCCCATTT A G C1orf105 Ensembl:ENSG00000180999 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs566587410 Functional Loss SNV dbSNP153 33..33 33 - - - 43440 RMVar_ID_43440 Human_SNP_ID_38932656 A-to-I Human chr1 + 172548918 172548918 172548918 TTTTGTCCACTTAATCTGTTATTTTGTGAGGTAATTTAAAATAGACCACCATACTTTTTGTTTAT TTTTGTCCACTTAATCTGTTATTTTGTGAGGTGATTTAAAATAGACCACCATACTTTTTGTTTAT A G SUCO Ensembl:ENSG00000094975 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs768857641 Functional Loss SNV dbSNP153 33..33 33 - - - 43441 RMVar_ID_43441 Human_SNP_ID_38981241 A-to-I Human chr1 - 172749033 172749033 172749033 TCTCATAGCCATATTTCCCACTCTCATAGCACATCTTGATTACAGTGATGGGTAACATACAGACC TCTCATAGCCATATTTCCCACTCTCATAGCACCTCTTGATTACAGTGATGGGTAACATACAGACC T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs753761411 Functional Loss SNV dbSNP153 33..33 33 - - - 43442 RMVar_ID_43442 Human_SNP_ID_39130589 A-to-I Human chr1 - 173402955 173402955 173402955 CCAGCTACTCAGGCAGCTGAGGTTGGAGGATCACTTGAGCCTGGGAGGTTGAGGCTGTGGTGAGC CCAGCTACTCAGGCAGCTGAGGTTGGAGGATCGCTTGAGCCTGGGAGGTTGAGGCTGTGGTGAGC T C LOC100506023,LOC100506023:2 RNACentral:URS00009B3372,RNACentral:URS000075CB0B lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1271334148 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_137630 43443 RMVar_ID_43443 Human_SNP_ID_39142211 A-to-I Human chr1 - 173454581 173454581 173454581 GGTCAATTGTCATCATATTCCAGTGGTGTGGAAGTGGCAGCCAGTCTGTGAATATAACTCTGGCC GGTCAATTGTCATCATATTCCAGTGGTGTGGAGGTGGCAGCCAGTCTGTGAATATAACTCTGGCC T C AL645568.1 Ensembl:ENSG00000203739 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1218719636 Functional Loss SNV dbSNP153 33..33 33 - - - 43444 RMVar_ID_43444 Human_SNP_ID_39142217 A-to-I Human chr1 - 173454597 173454597 173454597 CTAGACCCATAACTAGGGTCAATTGTCATCATATTCCAGTGGTGTGGAAGTGGCAGCCAGTCTGT CTAGACCCATAACTAGGGTCAATTGTCATCATGTTCCAGTGGTGTGGAAGTGGCAGCCAGTCTGT T C AL645568.1 Ensembl:ENSG00000203739 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1357267077 Functional Loss SNV dbSNP153 33..33 33 - - - 43445 RMVar_ID_43445 Human_SNP_ID_39142224 A-to-I Human chr1 - 173454615 173454615 173454615 AAACACCCGTTACTGCTGCTAGACCCATAACTAGGGTCAATTGTCATCATATTCCAGTGGTGTGG AAACACCCGTTACTGCTGCTAGACCCATAACTGGGGTCAATTGTCATCATATTCCAGTGGTGTGG T C AL645568.1 Ensembl:ENSG00000203739 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1412282269 Functional Loss SNV dbSNP153 33..33 33 - - - 43446 RMVar_ID_43446 Human_SNP_ID_39145429 A-to-I Human chr1 - 173468874 173468874 173468874 GGTACATTTGACTAGCCTGGTATCTGGTTGATATGGTTGACTGTGTCCCCACCCAAATCTCATCT GGTACATTTGACTAGCCTGGTATCTGGTTGATGTGGTTGACTGTGTCCCCACCCAAATCTCATCT T C AL645568.1 Ensembl:ENSG00000203739 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956540473 Functional Loss SNV dbSNP153 33..33 33 - - - 43447 RMVar_ID_43447 Human_SNP_ID_39201616 A-to-I Human chr1 + 173718137 173718137 173718137 TTTTGTAGATACAGGGTTTTGCCATGTTGCCCAGGTTGGTCTCAAACTCCTGGGCTCAAGCAGTC TTTTGTAGATACAGGGTTTTGCCATGTTGCCCGGGTTGGTCTCAAACTCCTGGGCTCAAGCAGTC A G KLHL20 Ensembl:ENSG00000076321 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1451233321 Functional Loss SNV dbSNP153 33..33 33 - - - 43448 RMVar_ID_43448 Human_SNP_ID_39203058 A-to-I Human chr1 + 173724698 173724698 173724698 ATGGTGACTCACACCTGTAGTCCCAGCTACTTAGGGGGCTGAGGTGGGAGGATCAGTTGAGCCTA ATGGTGACTCACACCTGTAGTCCCAGCTACTTTGGGGGCTGAGGTGGGAGGATCAGTTGAGCCTA A T KLHL20 Ensembl:ENSG00000076321 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1259026393 Functional Loss SNV dbSNP153 33..33 33 - - - 43449 RMVar_ID_43449 Human_SNP_ID_39214098 A-to-I Human chr1 + 173772994 173772994 173772994 TAAGAGACTTTTTAATTTAATCTGATTTTTTTAGAGACAGGGTCTCACTCTGTCACCCAGGCTGG TAAGAGACTTTTTAATTTAATCTGATTTTTTTTGAGACAGGGTCTCACTCTGTCACCCAGGCTGG A T KLHL20 Ensembl:ENSG00000076321 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941025437 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_30403,RMVar_hsa_circ_323547,RMVar_hsa_circ_351821,RMVar_hsa_circ_282179,RMVar_hsa_circ_29941,RMVar_hsa_circ_137657,RMVar_hsa_circ_137658,RMVar_hsa_circ_69176,RMVar_hsa_circ_339448,RMVar_hsa_circ_137660 43450 RMVar_ID_43450 Human_SNP_ID_39219380 A-to-I Human chr1 - 173796706 173796706 173796706 TTTGGTAGAGATGGGGTTTCAGTATATTGCCCAGGCTGGTCTTTAACCCTTCCCACCTGAGCCGA TTTGGTAGAGATGGGGTTTCAGTATATTGCCCGGGCTGGTCTTTAACCCTTCCCACCTGAGCCGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1176446301 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17731327,Human_RBP_ID_27391230 43451 RMVar_ID_43451 Human_SNP_ID_39219998 A-to-I Human chr1 - 173800000 173800000 173800000 CAATAATTAGCTGGGCGTGGTGGCACATGCCTATGATCCCAGCTACTGGGGAGGCTGAGGCAGGA CAATAATTAGCTGGGCGTGGTGGCACATGCCTGTGATCCCAGCTACTGGGGAGGCTGAGGCAGGA T C CENPL Ensembl:ENSG00000120334 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs997281165 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4008827,Human_RBP_ID_24607428,Human_RBP_ID_26372015 43452 RMVar_ID_43452 Human_SNP_ID_39219999 A-to-I Human chr1 - 173800000 173800000 173800000 CAATAATTAGCTGGGCGTGGTGGCACATGCCTATGATCCCAGCTACTGGGGAGGCTGAGGCAGGA CAATAATTAGCTGGGCGTGGTGGCACATGCCTCTGATCCCAGCTACTGGGGAGGCTGAGGCAGGA T G CENPL Ensembl:ENSG00000120334 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs997281165 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4008827,Human_RBP_ID_24607428,Human_RBP_ID_26372015 43453 RMVar_ID_43453 Human_SNP_ID_39221456 A-to-I Human chr1 - 173806521 173806521 173806521 GGAGTACAGTGGCACGATCTTGGTTGACTGCAACCTCTGTCTCCTGGGCTCAAGTGATCCTTCCA GGAGTACAGTGGCACGATCTTGGTTGACTGCACCCTCTGTCTCCTGGGCTCAAGTGATCCTTCCA T G CENPL Ensembl:ENSG00000120334 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs958719672 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10657207 Human_Splice_Rec_158552,Human_Splice_Rec_158553,Human_Splice_Rec_158580,Human_Splice_Rec_158581 RMVar_hsa_circ_38363 43454 RMVar_ID_43454 Human_SNP_ID_39226085 A-to-I Human chr1 + 173825333 173825333 173825333 GATCTGGGGTTCTCTCTACAGAAGTCTGTTGCAGAGTTCACAGAGGAGAATTCCAGGTGAAAATA GATCTGGGGTTCTCTCTACAGAAGTCTGTTGCGGAGTTCACAGAGGAGAATTCCAGGTGAAAATA A G DARS2 Ensembl:ENSG00000117593 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1226046698 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1415809 Human_Splice_Rec_158611,Human_Splice_Rec_158637,Human_Splice_Rec_158667,Human_Splice_Rec_158689,Human_Splice_Rec_158717,Human_Splice_Rec_158747,Human_Splice_Rec_158779,Human_Splice_Rec_158807,Human_Splice_Rec_158837,Human_Splice_Rec_158865,Human_Splice_Rec_158869,Human_Splice_Rec_158895 43455 RMVar_ID_43455 Human_SNP_ID_39231033 A-to-I Human chr1 + 173844959 173844948 173844959 GGGATTTCAGGCACCTGCCACCATACCAGACTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCA GGGATTTCAGGCACCTGCCACC___________ATTTTTGTATTTTTAGTAGAGACGGGGTTTCA CATACCAGACTA C DARS2 Ensembl:ENSG00000117593 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1197665443 Functional Loss DEL dbSNP153 23..33 33 - - - RMVar_hsa_circ_367042,RMVar_hsa_circ_25061,RMVar_hsa_circ_123054,RMVar_hsa_circ_326594,RMVar_hsa_circ_57942,RMVar_hsa_circ_137665,RMVar_hsa_circ_313271,RMVar_hsa_circ_289218,RMVar_hsa_circ_137668,RMVar_hsa_circ_137667,RMVar_hsa_circ_365795,RMVar_hsa_circ_79348,RMVar_hsa_circ_347853,RMVar_hsa_circ_337911,RMVar_hsa_circ_115202,RMVar_hsa_circ_137670,RMVar_hsa_circ_137673,RMVar_hsa_circ_267149,RMVar_hsa_circ_295180,RMVar_hsa_circ_310964,RMVar_hsa_circ_294409 43456 RMVar_ID_43456 Human_SNP_ID_39231043 A-to-I Human chr1 + 173844977 173844977 173844977 CACCATACCAGACTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGTCGGGCTGG CACCATACCAGACTAATTTTTGTATTTTTAGTGGAGACGGGGTTTCACCATGTTGGTCGGGCTGG A G DARS2 Ensembl:ENSG00000117593 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1177486926 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_367042,RMVar_hsa_circ_25061,RMVar_hsa_circ_123054,RMVar_hsa_circ_326594,RMVar_hsa_circ_57942,RMVar_hsa_circ_137665,RMVar_hsa_circ_313271,RMVar_hsa_circ_289218,RMVar_hsa_circ_137668,RMVar_hsa_circ_137667,RMVar_hsa_circ_365795,RMVar_hsa_circ_79348,RMVar_hsa_circ_347853,RMVar_hsa_circ_337911,RMVar_hsa_circ_115202,RMVar_hsa_circ_137670,RMVar_hsa_circ_137673,RMVar_hsa_circ_267149,RMVar_hsa_circ_295180,RMVar_hsa_circ_310964,RMVar_hsa_circ_294409 43457 RMVar_ID_43457 Human_SNP_ID_39231173 A-to-I Human chr1 + 173845463 173845462 173845463 TATTTATATATTTATTTTGAAGATGTAGTCTTATTCTGTCGCCCAGGCTAGAGTGCAGTGTTGCC TATTTATATATTTATTTTGAAGATGTAGTCTT_TTCTGTCGCCCAGGCTAGAGTGCAGTGTTGCC TA T DARS2 Ensembl:ENSG00000117593 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1422862043 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_25061,RMVar_hsa_circ_123054,RMVar_hsa_circ_326594,RMVar_hsa_circ_57942,RMVar_hsa_circ_137665,RMVar_hsa_circ_313271,RMVar_hsa_circ_289218,RMVar_hsa_circ_137668,RMVar_hsa_circ_137667,RMVar_hsa_circ_79348,RMVar_hsa_circ_337911,RMVar_hsa_circ_115202,RMVar_hsa_circ_137670,RMVar_hsa_circ_267149,RMVar_hsa_circ_137674,RMVar_hsa_circ_282274,RMVar_hsa_circ_351548 43458 RMVar_ID_43458 Human_SNP_ID_39234131 A-to-I Human chr1 - 173857926 173857926 173857926 ATCTTTCACACCTAAGTAAAAAGGAACTTCAAAAAAAGTCCTAACCAAAAAAAATCCAAATGATG ATCTTTCACACCTAAGTAAAAAGGAACTTCAAGAAAAGTCCTAACCAAAAAAAATCCAAATGATG T C GAS5 RNACentral:URS0000D57C9D lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs760958796 Functional Loss SNV dbSNP153 33..33 33 - - - 43459 RMVar_ID_43459 Human_SNP_ID_39234383 A-to-I Human chr1 + 173859077 173859077 173859077 TAAAATGAGGCCGGGTACAGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCTGAGGCAGAC TAAAATGAGGCCGGGTACAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGAC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1203142495 Functional Loss SNV dbSNP153 33..33 33 - - - 43460 RMVar_ID_43460 Human_SNP_ID_39234529 A-to-I Human chr1 + 173859748 173859748 173859748 CTCACTTCATCCTCCACCTCCCGGGTTCAGGCAGTTTTCCTGCCTCAGCCTCCTGAGTAGTTGGG CTCACTTCATCCTCCACCTCCCGGGTTCAGGCGGTTTTCCTGCCTCAGCCTCCTGAGTAGTTGGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1261837502 Functional Loss SNV dbSNP153 33..33 33 - - - 43461 RMVar_ID_43461 Human_SNP_ID_39234539 A-to-I Human chr1 + 173859819 173859819 173859819 GGTGCCCTCCACCACACCTGGTTAATTTTTGTATTTTTAGTAGAGACGAGGTTTTGCCATGTTGA GGTGCCCTCCACCACACCTGGTTAATTTTTGTGTTTTTAGTAGAGACGAGGTTTTGCCATGTTGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893958689 Functional Loss SNV dbSNP153 33..33 33 - - - 43462 RMVar_ID_43462 Human_SNP_ID_39234858 A-to-I Human chr1 - 173861217 173861216 173861217 AAGCATATTAAAAGATTTCAGTTGTATGTAGTAGCTCATGCCTGTAATCCCAACACTTTGGGAAA AAGCATATTAAAAGATTTCAGTTGTATGTAGT_GCTCATGCCTGTAATCCCAACACTTTGGGAAA CT C GAS5 Ensembl:ENSG00000234741 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs768635249 Functional Loss DEL dbSNP153 33..33 33 - - - 43463 RMVar_ID_43463 Human_SNP_ID_39235024 A-to-I Human chr1 + 173861633 173861633 173861633 AGAATAGAACTTGGCTGGATGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGGCAGGGC AGAATAGAACTTGGCTGGATGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGGCAGGGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1434549664 Functional Loss SNV dbSNP153 33..33 33 - - - 43464 RMVar_ID_43464 Human_SNP_ID_39235117 A-to-I Human chr1 - 173861918 173861918 173861918 CTGAAAAAAAGCGAAAATTAGCCGGGTGTGGTAGTGTGGGCCTGTAGTCCCAGCTACTCTGAACC CTGAAAAAAAGCGAAAATTAGCCGGGTGTGGTGGTGTGGGCCTGTAGTCCCAGCTACTCTGAACC T C GAS5 Ensembl:ENSG00000234741 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053070023 Functional Loss SNV dbSNP153 33..33 33 - - - 43465 RMVar_ID_43465 Human_SNP_ID_39235118 A-to-I Human chr1 - 173861918 173861918 173861918 CTGAAAAAAAGCGAAAATTAGCCGGGTGTGGTAGTGTGGGCCTGTAGTCCCAGCTACTCTGAACC CTGAAAAAAAGCGAAAATTAGCCGGGTGTGGTCGTGTGGGCCTGTAGTCCCAGCTACTCTGAACC T G GAS5 Ensembl:ENSG00000234741 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053070023 Functional Loss SNV dbSNP153 33..33 33 - - - 43466 RMVar_ID_43466 Human_SNP_ID_39235587 A-to-I Human chr1 + 173863131 173863131 173863131 CCAAAATGAGTTGGTTGTGATGGTAGGTGCCTATAGTCCTAGCTACAAGAGGCTGAAGAGAATCG CCAAAATGAGTTGGTTGTGATGGTAGGTGCCTGTAGTCCTAGCTACAAGAGGCTGAAGAGAATCG A G GAS5-AS1 Ensembl:ENSG00000270084 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991887985 Functional Loss SNV dbSNP153 33..33 33 - - - 43467 RMVar_ID_43467 Human_SNP_ID_39235618 A-to-I Human chr1 + 173863209 173863209 173863209 GGTAGAGGTTGCAGTGAGCAGCGGTTGAGATCATGCCATTGCACTCCAGCCTGGGCAACAGGATT GGTAGAGGTTGCAGTGAGCAGCGGTTGAGATCGTGCCATTGCACTCCAGCCTGGGCAACAGGATT A G GAS5-AS1 Ensembl:ENSG00000270084 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1374814301 Functional Loss SNV dbSNP153 33..33 33 - - - 43468 RMVar_ID_43468 Human_SNP_ID_39235906 A-to-I Human chr1 - 173864059 173864059 173864059 TTATTTTTTGAGACAGGGTCTTGCCTCACCCAAGCTAGAGTGCAGTGGCCTTTGAAGCTTACTAC TTATTTTTTGAGACAGGGTCTTGCCTCACCCAGGCTAGAGTGCAGTGGCCTTTGAAGCTTACTAC T C GAS5 Ensembl:ENSG00000234741 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1476554786 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_333453,Human_RBP_ID_851890,Human_RBP_ID_1438432,Human_RBP_ID_1729572,Human_RBP_ID_2105067,Human_RBP_ID_5086318,Human_RBP_ID_5091844,Human_RBP_ID_5642814,Human_RBP_ID_8171834,Human_RBP_ID_8242100,Human_RBP_ID_8290779,Human_RBP_ID_8958688,Human_RBP_ID_9343092,Human_RBP_ID_9357172,Human_RBP_ID_10657818,Human_RBP_ID_17731433,Human_RBP_ID_18219859,Human_RBP_ID_19035727,Human_RBP_ID_22560720,Human_RBP_ID_23205442,Human_RBP_ID_23345772,Human_RBP_ID_24607661,Human_RBP_ID_26847288 Human_Splice_Rec_158968,Human_Splice_Rec_158980,Human_Splice_Rec_159000,Human_Splice_Rec_159018,Human_Splice_Rec_159050,Human_Splice_Rec_159072,Human_Splice_Rec_159090,Human_Splice_Rec_159104,Human_Splice_Rec_159124,Human_Splice_Rec_159148,Human_Splice_Rec_159152,Human_Splice_Rec_159174,Human_Splice_Rec_159196,Human_Splice_Rec_159204,Human_Splice_Rec_159228,Human_Splice_Rec_159250 Human_miRNA_ID_1968096,Human_miRNA_ID_3148125 RMVar_hsa_circ_120625,RMVar_hsa_circ_81779,RMVar_hsa_circ_101967,RMVar_hsa_circ_111329,RMVar_hsa_circ_89160,RMVar_hsa_circ_137676,RMVar_hsa_circ_137678,RMVar_hsa_circ_137679,RMVar_hsa_circ_137680,RMVar_hsa_circ_137677 43469 RMVar_ID_43469 Human_SNP_ID_39235916 A-to-I Human chr1 - 173864077 173864077 173864077 GTGGCTAAAAGTCTTGTCTTATTTTTTGAGACAGGGTCTTGCCTCACCCAAGCTAGAGTGCAGTG GTGGCTAAAAGTCTTGTCTTATTTTTTGAGACGGGGTCTTGCCTCACCCAAGCTAGAGTGCAGTG T C GAS5 Ensembl:ENSG00000234741 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs11537772 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_333453,Human_RBP_ID_851890,Human_RBP_ID_1729573,Human_RBP_ID_2105068,Human_RBP_ID_3287248,Human_RBP_ID_5272952,Human_RBP_ID_8171834,Human_RBP_ID_8290779,Human_RBP_ID_10657819,Human_RBP_ID_18556471,Human_RBP_ID_22560720 Human_miRNA_ID_3147066,Human_miRNA_ID_3147149,Human_miRNA_ID_3169947,Human_miRNA_ID_3176029 RMVar_hsa_circ_120625,RMVar_hsa_circ_81779,RMVar_hsa_circ_101967,RMVar_hsa_circ_111329,RMVar_hsa_circ_89160,RMVar_hsa_circ_137676,RMVar_hsa_circ_137678,RMVar_hsa_circ_137679,RMVar_hsa_circ_137680,RMVar_hsa_circ_137677 43470 RMVar_ID_43470 Human_SNP_ID_39236302 A-to-I Human chr1 - 173865037 173865037 173865037 GTGACACCATGCCTGGCTAATTTTGTACAGCTATGTTGTCCAGGCTGGTCTCGAACTCTTGACCT GTGACACCATGCCTGGCTAATTTTGTACAGCTTTGTTGTCCAGGCTGGTCTCGAACTCTTGACCT T A GAS5 Ensembl:ENSG00000234741 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs747913096 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_333481,Human_RBP_ID_1150653,Human_RBP_ID_1415851,Human_RBP_ID_1729588,Human_RBP_ID_2105115,Human_RBP_ID_5245476,Human_RBP_ID_8290803,Human_RBP_ID_10657897,Human_RBP_ID_24448507 Human_miRNA_ID_3179744 RMVar_hsa_circ_108561,RMVar_hsa_circ_120625,RMVar_hsa_circ_81779,RMVar_hsa_circ_101967,RMVar_hsa_circ_111329,RMVar_hsa_circ_137678,RMVar_hsa_circ_137679,RMVar_hsa_circ_137680,RMVar_hsa_circ_137677,RMVar_hsa_circ_375566,RMVar_hsa_circ_338727,RMVar_hsa_circ_125218,RMVar_hsa_circ_137683,RMVar_hsa_circ_81617,RMVar_hsa_circ_92595,RMVar_hsa_circ_100440,RMVar_hsa_circ_86669,RMVar_hsa_circ_137685,RMVar_hsa_circ_137687,RMVar_hsa_circ_137688,RMVar_hsa_circ_137686,RMVar_hsa_circ_137684,RMVar_hsa_circ_110588,RMVar_hsa_circ_137681,RMVar_hsa_circ_137682,RMVar_hsa_circ_360027,RMVar_hsa_circ_54258,RMVar_hsa_circ_137691 43471 RMVar_ID_43471 Human_SNP_ID_39236303 A-to-I Human chr1 - 173865037 173865037 173865037 GTGACACCATGCCTGGCTAATTTTGTACAGCTATGTTGTCCAGGCTGGTCTCGAACTCTTGACCT GTGACACCATGCCTGGCTAATTTTGTACAGCTGTGTTGTCCAGGCTGGTCTCGAACTCTTGACCT T C GAS5 Ensembl:ENSG00000234741 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs747913096 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_333481,Human_RBP_ID_1150653,Human_RBP_ID_1415851,Human_RBP_ID_1729588,Human_RBP_ID_2105115,Human_RBP_ID_5245476,Human_RBP_ID_8290803,Human_RBP_ID_10657897,Human_RBP_ID_24448507 Human_miRNA_ID_3179744 RMVar_hsa_circ_108561,RMVar_hsa_circ_120625,RMVar_hsa_circ_81779,RMVar_hsa_circ_101967,RMVar_hsa_circ_111329,RMVar_hsa_circ_137678,RMVar_hsa_circ_137679,RMVar_hsa_circ_137680,RMVar_hsa_circ_137677,RMVar_hsa_circ_375566,RMVar_hsa_circ_338727,RMVar_hsa_circ_125218,RMVar_hsa_circ_137683,RMVar_hsa_circ_81617,RMVar_hsa_circ_92595,RMVar_hsa_circ_100440,RMVar_hsa_circ_86669,RMVar_hsa_circ_137685,RMVar_hsa_circ_137687,RMVar_hsa_circ_137688,RMVar_hsa_circ_137686,RMVar_hsa_circ_137684,RMVar_hsa_circ_110588,RMVar_hsa_circ_137681,RMVar_hsa_circ_137682,RMVar_hsa_circ_360027,RMVar_hsa_circ_54258,RMVar_hsa_circ_137691 43472 RMVar_ID_43472 Human_SNP_ID_39237273 A-to-I Human chr1 - 173867303 173867303 173867303 GTTGGCGAGACTGGTCTTGAACTCCTGACCTCAGGTGATCCACCAGCCGTGGTCCCCCAACATAC GTTGGCGAGACTGGTCTTGAACTCCTGACCTCTGGTGATCCACCAGCCGTGGTCCCCCAACATAC T A GAS5 Ensembl:ENSG00000234741 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs773617276 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5245481,Human_RBP_ID_8243945,Human_RBP_ID_10658032 Human_miRNA_ID_3152825 RMVar_hsa_circ_81779,RMVar_hsa_circ_137680,RMVar_hsa_circ_100440,RMVar_hsa_circ_137681,RMVar_hsa_circ_90147,RMVar_hsa_circ_137696,RMVar_hsa_circ_108405,RMVar_hsa_circ_137703 43473 RMVar_ID_43473 Human_SNP_ID_39255887 A-to-I Human chr1 - 173940997 173940997 173940997 GCCAGCATGGTGAAACCCCGTCTCTACTAAAAATACAAAGATTAGTTTGGTGTGGTGGCATGTGC GCCAGCATGGTGAAACCCCGTCTCTACTAAAAGTACAAAGATTAGTTTGGTGTGGTGGCATGTGC T C RC3H1 Ensembl:ENSG00000135870 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs933879127 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_137705,RMVar_hsa_circ_102731 43474 RMVar_ID_43474 Human_SNP_ID_39256733 A-to-I Human chr1 - 173944058 173944058 173944058 CTCCTGGGCTCAAGTGATCCTCCCTAGTAGCTAGGACTACGGGCCCACACCACCATCCCAGGCTA CTCCTGGGCTCAAGTGATCCTCCCTAGTAGCTTGGACTACGGGCCCACACCACCATCCCAGGCTA T A RC3H1 Ensembl:ENSG00000135870 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1279791403 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5715801 RMVar_hsa_circ_39148,RMVar_hsa_circ_137705,RMVar_hsa_circ_102731,RMVar_hsa_circ_320207,RMVar_hsa_circ_364924,RMVar_hsa_circ_339168,RMVar_hsa_circ_268902,RMVar_hsa_circ_64026,RMVar_hsa_circ_137708,RMVar_hsa_circ_72273,RMVar_hsa_circ_360160 43475 RMVar_ID_43475 Human_SNP_ID_39256734 A-to-I Human chr1 - 173944058 173944058 173944058 CTCCTGGGCTCAAGTGATCCTCCCTAGTAGCTAGGACTACGGGCCCACACCACCATCCCAGGCTA CTCCTGGGCTCAAGTGATCCTCCCTAGTAGCTGGGACTACGGGCCCACACCACCATCCCAGGCTA T C RC3H1 Ensembl:ENSG00000135870 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1279791403 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5715801 RMVar_hsa_circ_39148,RMVar_hsa_circ_137705,RMVar_hsa_circ_102731,RMVar_hsa_circ_320207,RMVar_hsa_circ_364924,RMVar_hsa_circ_339168,RMVar_hsa_circ_268902,RMVar_hsa_circ_64026,RMVar_hsa_circ_137708,RMVar_hsa_circ_72273,RMVar_hsa_circ_360160 43476 RMVar_ID_43476 Human_SNP_ID_39257015 A-to-I Human chr1 - 173945277 173945277 173945277 TACAAAAAGTGCAAAAATTGGCCAGGCATGGTAGTGCACGCCTGTAGTCTCAGCTACTCAGGAGG TACAAAAAGTGCAAAAATTGGCCAGGCATGGTGGTGCACGCCTGTAGTCTCAGCTACTCAGGAGG T C RC3H1 Ensembl:ENSG00000135870 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1004278347 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39148,RMVar_hsa_circ_137705,RMVar_hsa_circ_102731,RMVar_hsa_circ_320207,RMVar_hsa_circ_364924,RMVar_hsa_circ_339168,RMVar_hsa_circ_268902,RMVar_hsa_circ_64026,RMVar_hsa_circ_137708,RMVar_hsa_circ_72273,RMVar_hsa_circ_360160 43477 RMVar_ID_43477 Human_SNP_ID_39257041 A-to-I Human chr1 - 173945407 173945407 173945407 AATTTTTAAAATCTGGCTGGACGTGGTGGTTCATGCTTGTAATCCCAGCACTTTGGGAGGCCAGA AATTTTTAAAATCTGGCTGGACGTGGTGGTTCGTGCTTGTAATCCCAGCACTTTGGGAGGCCAGA T C RC3H1 Ensembl:ENSG00000135870 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1318097502 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10659103 RMVar_hsa_circ_39148,RMVar_hsa_circ_137705,RMVar_hsa_circ_102731,RMVar_hsa_circ_320207,RMVar_hsa_circ_364924,RMVar_hsa_circ_339168,RMVar_hsa_circ_268902,RMVar_hsa_circ_64026,RMVar_hsa_circ_137708,RMVar_hsa_circ_72273,RMVar_hsa_circ_360160 43478 RMVar_ID_43478 Human_SNP_ID_39257133 A-to-I Human chr1 - 173945776 173945776 173945776 GTGAACCCAGGAAGCAGAGGTTGCAGTGAGCCAAGATTGCGCCATTGCACTCCAGCCCAGGCTAC GTGAACCCAGGAAGCAGAGGTTGCAGTGAGCCCAGATTGCGCCATTGCACTCCAGCCCAGGCTAC T G RC3H1 Ensembl:ENSG00000135870 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1051311965 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39148,RMVar_hsa_circ_137705,RMVar_hsa_circ_102731,RMVar_hsa_circ_320207,RMVar_hsa_circ_364924,RMVar_hsa_circ_339168,RMVar_hsa_circ_268902,RMVar_hsa_circ_64026,RMVar_hsa_circ_137708,RMVar_hsa_circ_72273,RMVar_hsa_circ_360160 43479 RMVar_ID_43479 Human_SNP_ID_39257176 A-to-I Human chr1 - 173945952 173945952 173945952 CTGTAATCCCAGCACTTTGGGAGGCCGAGGCAAGTGGATCACAAGATCAGGAGTTTGAGAACAGT CTGTAATCCCAGCACTTTGGGAGGCCGAGGCACGTGGATCACAAGATCAGGAGTTTGAGAACAGT T G RC3H1 Ensembl:ENSG00000135870 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs974492063 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10659120 RMVar_hsa_circ_39148,RMVar_hsa_circ_137705,RMVar_hsa_circ_102731,RMVar_hsa_circ_320207,RMVar_hsa_circ_364924,RMVar_hsa_circ_339168,RMVar_hsa_circ_268902,RMVar_hsa_circ_64026,RMVar_hsa_circ_137708,RMVar_hsa_circ_72273,RMVar_hsa_circ_360160 43480 RMVar_ID_43480 Human_SNP_ID_39257188 A-to-I Human chr1 - 173946005 173946005 173946005 ACCACCATACTCAGCGAATTTTTTGTATTTTTAGTAGAGATAGGGTTTCACCCCTGTAATCCCAG ACCACCATACTCAGCGAATTTTTTGTATTTTTGGTAGAGATAGGGTTTCACCCCTGTAATCCCAG T C RC3H1 Ensembl:ENSG00000135870 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1412642299 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39148,RMVar_hsa_circ_137705,RMVar_hsa_circ_102731,RMVar_hsa_circ_320207,RMVar_hsa_circ_364924,RMVar_hsa_circ_339168,RMVar_hsa_circ_268902,RMVar_hsa_circ_64026,RMVar_hsa_circ_137708,RMVar_hsa_circ_72273,RMVar_hsa_circ_360160 43481 RMVar_ID_43481 Human_SNP_ID_39257200 A-to-I Human chr1 - 173946047 173946047 173946047 CTCCTGCCTCAGCCTCCTGAGTGGTTGGGGTTATAGATGTACACCACCATACTCAGCGAATTTTT CTCCTGCCTCAGCCTCCTGAGTGGTTGGGGTTGTAGATGTACACCACCATACTCAGCGAATTTTT T C RC3H1 Ensembl:ENSG00000135870 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1374804850 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39148,RMVar_hsa_circ_137705,RMVar_hsa_circ_102731,RMVar_hsa_circ_320207,RMVar_hsa_circ_364924,RMVar_hsa_circ_339168,RMVar_hsa_circ_268902,RMVar_hsa_circ_64026,RMVar_hsa_circ_137708,RMVar_hsa_circ_72273,RMVar_hsa_circ_360160 43482 RMVar_ID_43482 Human_SNP_ID_39257211 A-to-I Human chr1 - 173946082 173946082 173946082 TCACTGCAACCTCCACCTCCTGGGTTCATGCAATTCTCCTGCCTCAGCCTCCTGAGTGGTTGGGG TCACTGCAACCTCCACCTCCTGGGTTCATGCAGTTCTCCTGCCTCAGCCTCCTGAGTGGTTGGGG T C RC3H1 Ensembl:ENSG00000135870 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs536630966 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39148,RMVar_hsa_circ_137705,RMVar_hsa_circ_102731,RMVar_hsa_circ_320207,RMVar_hsa_circ_364924,RMVar_hsa_circ_339168,RMVar_hsa_circ_268902,RMVar_hsa_circ_64026,RMVar_hsa_circ_137708,RMVar_hsa_circ_72273,RMVar_hsa_circ_360160 43483 RMVar_ID_43483 Human_SNP_ID_39260150 A-to-I Human chr1 - 173957699 173957699 173957699 TAAAAATGAGCTAGGTGTGGTGGGACACGCCTACAGTCCCAGCTACTTGGGAGGCTGAGGTGGGA TAAAAATGAGCTAGGTGTGGTGGGACACGCCTGCAGTCCCAGCTACTTGGGAGGCTGAGGTGGGA T C RC3H1 Ensembl:ENSG00000135870 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1235632083 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5715852,Human_RBP_ID_24608004 RMVar_hsa_circ_39148,RMVar_hsa_circ_137705,RMVar_hsa_circ_102731,RMVar_hsa_circ_320207,RMVar_hsa_circ_339168,RMVar_hsa_circ_64026,RMVar_hsa_circ_137708,RMVar_hsa_circ_341364,RMVar_hsa_circ_330383,RMVar_hsa_circ_279234,RMVar_hsa_circ_137710,RMVar_hsa_circ_28555,RMVar_hsa_circ_4587,RMVar_hsa_circ_365557,RMVar_hsa_circ_137709,RMVar_hsa_circ_365729,RMVar_hsa_circ_137715 43484 RMVar_ID_43484 Human_SNP_ID_39264483 A-to-I Human chr1 - 173976254 173976254 173976254 TTTAGTATCTTTAGTAGAAACAGGGTTTCACCATCTTGGCCAGGCTGTTCTCAAACTCCTGAACT TTTAGTATCTTTAGTAGAAACAGGGTTTCACCGTCTTGGCCAGGCTGTTCTCAAACTCCTGAACT T C RC3H1 Ensembl:ENSG00000135870 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs867355379 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126,RMVar_hsa_circ_137705,RMVar_hsa_circ_102731,RMVar_hsa_circ_320207,RMVar_hsa_circ_64026,RMVar_hsa_circ_137708,RMVar_hsa_circ_330383,RMVar_hsa_circ_279234,RMVar_hsa_circ_4587,RMVar_hsa_circ_365557,RMVar_hsa_circ_137709,RMVar_hsa_circ_137715,RMVar_hsa_circ_283068,RMVar_hsa_circ_319073,RMVar_hsa_circ_137716,RMVar_hsa_circ_371902,RMVar_hsa_circ_285022,RMVar_hsa_circ_137719,RMVar_hsa_circ_137721,RMVar_hsa_circ_293840,RMVar_hsa_circ_307354,RMVar_hsa_circ_273327,RMVar_hsa_circ_137720,RMVar_hsa_circ_299576 43485 RMVar_ID_43485 Human_SNP_ID_39264530 A-to-I Human chr1 - 173976438 173976438 173976438 AACTTTTTTTTTTTTTTTGGAGATACAGTTTCACTCTGTCCCCCAGGCTGGAGGCAATGGCAAGA AACTTTTTTTTTTTTTTTGGAGATACAGTTTCGCTCTGTCCCCCAGGCTGGAGGCAATGGCAAGA T C RC3H1 Ensembl:ENSG00000135870 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1437278455 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126,RMVar_hsa_circ_137705,RMVar_hsa_circ_102731,RMVar_hsa_circ_320207,RMVar_hsa_circ_64026,RMVar_hsa_circ_137708,RMVar_hsa_circ_330383,RMVar_hsa_circ_279234,RMVar_hsa_circ_4587,RMVar_hsa_circ_365557,RMVar_hsa_circ_137709,RMVar_hsa_circ_137715,RMVar_hsa_circ_283068,RMVar_hsa_circ_319073,RMVar_hsa_circ_137716,RMVar_hsa_circ_371902,RMVar_hsa_circ_285022,RMVar_hsa_circ_137719,RMVar_hsa_circ_137721,RMVar_hsa_circ_293840,RMVar_hsa_circ_307354,RMVar_hsa_circ_273327,RMVar_hsa_circ_137720,RMVar_hsa_circ_299576 43486 RMVar_ID_43486 Human_SNP_ID_39265197 A-to-I Human chr1 - 173979397 173979397 173979397 GTCATCTGCCCACCACAGCCTCCCAAAGTGCTAGGATTACAGGCGTGAGCCACTGTGCCTGGCCT GTCATCTGCCCACCACAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGTGCCTGGCCT T C RC3H1 Ensembl:ENSG00000135870 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs567831099 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126,RMVar_hsa_circ_137705,RMVar_hsa_circ_102731,RMVar_hsa_circ_320207,RMVar_hsa_circ_137708,RMVar_hsa_circ_279234,RMVar_hsa_circ_365557,RMVar_hsa_circ_283068,RMVar_hsa_circ_319073,RMVar_hsa_circ_137716,RMVar_hsa_circ_285022,RMVar_hsa_circ_137721,RMVar_hsa_circ_293840,RMVar_hsa_circ_307354,RMVar_hsa_circ_137720,RMVar_hsa_circ_299576,RMVar_hsa_circ_137722,RMVar_hsa_circ_269283,RMVar_hsa_circ_320798,RMVar_hsa_circ_375056,RMVar_hsa_circ_137723 43487 RMVar_ID_43487 Human_SNP_ID_39265215 A-to-I Human chr1 - 173979480 173979480 173979480 TGTACCACGCCCAAATTTTTTGTATCTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGG TGTACCACGCCCAAATTTTTTGTATCTTTAGTTGAGACGGGGTTTCACCATGTTGGCCAGGCTGG T A RC3H1 Ensembl:ENSG00000135870 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs141038790 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126,RMVar_hsa_circ_137705,RMVar_hsa_circ_102731,RMVar_hsa_circ_320207,RMVar_hsa_circ_137708,RMVar_hsa_circ_279234,RMVar_hsa_circ_365557,RMVar_hsa_circ_283068,RMVar_hsa_circ_319073,RMVar_hsa_circ_137716,RMVar_hsa_circ_285022,RMVar_hsa_circ_137721,RMVar_hsa_circ_293840,RMVar_hsa_circ_307354,RMVar_hsa_circ_137720,RMVar_hsa_circ_299576,RMVar_hsa_circ_137722,RMVar_hsa_circ_269283,RMVar_hsa_circ_320798,RMVar_hsa_circ_375056,RMVar_hsa_circ_137723 43488 RMVar_ID_43488 Human_SNP_ID_39265216 A-to-I Human chr1 - 173979480 173979480 173979480 TGTACCACGCCCAAATTTTTTGTATCTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGG TGTACCACGCCCAAATTTTTTGTATCTTTAGTGGAGACGGGGTTTCACCATGTTGGCCAGGCTGG T C RC3H1 Ensembl:ENSG00000135870 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs141038790 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126,RMVar_hsa_circ_137705,RMVar_hsa_circ_102731,RMVar_hsa_circ_320207,RMVar_hsa_circ_137708,RMVar_hsa_circ_279234,RMVar_hsa_circ_365557,RMVar_hsa_circ_283068,RMVar_hsa_circ_319073,RMVar_hsa_circ_137716,RMVar_hsa_circ_285022,RMVar_hsa_circ_137721,RMVar_hsa_circ_293840,RMVar_hsa_circ_307354,RMVar_hsa_circ_137720,RMVar_hsa_circ_299576,RMVar_hsa_circ_137722,RMVar_hsa_circ_269283,RMVar_hsa_circ_320798,RMVar_hsa_circ_375056,RMVar_hsa_circ_137723 43489 RMVar_ID_43489 Human_SNP_ID_39268035 A-to-I Human chr1 - 173991027 173991027 173991027 CAGGGTTTCGCCATGTTGGCTATGCTGGTCTCAAGCTCCTGACCTCAAGTGATCCACCTGTCTCG CAGGGTTTCGCCATGTTGGCTATGCTGGTCTCGAGCTCCTGACCTCAAGTGATCCACCTGTCTCG T C RC3H1 Ensembl:ENSG00000135870 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1289831610 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24608216 RMVar_hsa_circ_320207,RMVar_hsa_circ_137708,RMVar_hsa_circ_279234,RMVar_hsa_circ_365557,RMVar_hsa_circ_283068,RMVar_hsa_circ_285022,RMVar_hsa_circ_299576,RMVar_hsa_circ_320798,RMVar_hsa_circ_137723,RMVar_hsa_circ_279622,RMVar_hsa_circ_137724,RMVar_hsa_circ_51921 43490 RMVar_ID_43490 Human_SNP_ID_39268877 A-to-I Human chr1 - 173994271 173994271 173994271 CTCCTTACTCAGCTTCCCGAGTTCCTGGGATTACAGCCATGCACCACCACACCTGGCTAATTTTT CTCCTTACTCAGCTTCCCGAGTTCCTGGGATTGCAGCCATGCACCACCACACCTGGCTAATTTTT T C RC3H1 Ensembl:ENSG00000135870 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1214128307 Functional Loss SNV dbSNP153 33..33 33 - - - 43491 RMVar_ID_43491 Human_SNP_ID_39270518 A-to-I Human chr1 - 174001539 174001539 174001539 CCAGCTACTCTGCATGAGAATGGCTTGAACCTAGGAGGTGGAGGTTGCAGTGAGCCAAAATCGTG CCAGCTACTCTGCATGAGAATGGCTTGAACCTTGGAGGTGGAGGTTGCAGTGAGCCAAAATCGTG T A RC3H1 Ensembl:ENSG00000135870 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1306650052 Functional Loss SNV dbSNP153 33..33 33 - - - 43492 RMVar_ID_43492 Human_SNP_ID_39270561 A-to-I Human chr1 - 174001712 174001712 174001712 AAGATGGTGCTTTTGGCTGGGCGTGGTGGCTCATGCCTATATAATCCCTGCACTTTGGGAGGCTG AAGATGGTGCTTTTGGCTGGGCGTGGTGGCTCGTGCCTATATAATCCCTGCACTTTGGGAGGCTG T C RC3H1 Ensembl:ENSG00000135870 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7518172 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9467795 43493 RMVar_ID_43493 Human_SNP_ID_39270841 A-to-I Human chr1 - 174003166 174003166 174003166 GCCAGGCTGGTCTCGAACTCCTGACCTCAGGTAATCCTCCACTTCAGCCTCCCAAAGTGTTGGGA GCCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCCTCCACTTCAGCCTCCCAAAGTGTTGGGA T C RC3H1 Ensembl:ENSG00000135870 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1419419323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23346114 43494 RMVar_ID_43494 Human_SNP_ID_39270865 A-to-I Human chr1 - 174003221 174003221 174003221 CACCATGTCTGGCTAATTTTTGCATTTTTAGTAGAGACGGGGTTTCACCACGTTGGCCAGGCTGG CACCATGTCTGGCTAATTTTTGCATTTTTAGTGGAGACGGGGTTTCACCACGTTGGCCAGGCTGG T C RC3H1 Ensembl:ENSG00000135870 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs181655601 Functional Loss SNV dbSNP153 33..33 33 - - - 43495 RMVar_ID_43495 Human_SNP_ID_39270866 A-to-I Human chr1 - 174003230 174003230 174003230 AGCGCCCACCACCATGTCTGGCTAATTTTTGCATTTTTAGTAGAGACGGGGTTTCACCACGTTGG AGCGCCCACCACCATGTCTGGCTAATTTTTGCGTTTTTAGTAGAGACGGGGTTTCACCACGTTGG T C RC3H1 Ensembl:ENSG00000135870 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs928152478 Functional Loss SNV dbSNP153 33..33 33 - - - 43496 RMVar_ID_43496 Human_SNP_ID_39271178 A-to-I Human chr1 - 174004250 174004250 174004250 AAAACTAACCAGGTGTGTTGGTGCACACCTATAGTCCTGGCTACTTGGGAGGCTGAGGTAAGAGG AAAACTAACCAGGTGTGTTGGTGCACACCTATGGTCCTGGCTACTTGGGAGGCTGAGGTAAGAGG T C RC3H1 Ensembl:ENSG00000135870 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs944836514 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10659949,Human_RBP_ID_24608360 43497 RMVar_ID_43497 Human_SNP_ID_39271179 A-to-I Human chr1 - 174004252 174004252 174004252 AAAAAACTAACCAGGTGTGTTGGTGCACACCTATAGTCCTGGCTACTTGGGAGGCTGAGGTAAGA AAAAAACTAACCAGGTGTGTTGGTGCACACCTGTAGTCCTGGCTACTTGGGAGGCTGAGGTAAGA T C RC3H1 Ensembl:ENSG00000135870 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1413374484 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24608361 43498 RMVar_ID_43498 Human_SNP_ID_39271340 A-to-I Human chr1 - 174004829 174004829 174004829 CCTTTGCATGTTACTCTGAATGGTAAGACCCTATCTTCCCTGGCAGCTTCCCATTAGCCCGATAG CCTTTGCATGTTACTCTGAATGGTAAGACCCTGTCTTCCCTGGCAGCTTCCCATTAGCCCGATAG T C RC3H1 Ensembl:ENSG00000135870 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs959907065 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24608367 43499 RMVar_ID_43499 Human_SNP_ID_39271387 A-to-I Human chr1 - 174004999 174004999 174004999 TATGGTTTTTAATACTTAGGAAGCTGTCCTATATATGTTAGCAAATCCATCAAGCTGGAGTATTC TATGGTTTTTAATACTTAGGAAGCTGTCCTATGTATGTTAGCAAATCCATCAAGCTGGAGTATTC T C RC3H1 Ensembl:ENSG00000135870 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs948045220 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2105332,Human_RBP_ID_9467819,Human_RBP_ID_17558042 43500 RMVar_ID_43500 Human_SNP_ID_39272430 A-to-I Human chr1 - 174009729 174009729 174009729 GGTTCAAGTGATTCTCGTGCCTCAGCCTTCCAAGTAGCTGAGACTACAGACGCGTGCCACCATAC GGTTCAAGTGATTCTCGTGCCTCAGCCTTCCAGGTAGCTGAGACTACAGACGCGTGCCACCATAC T C RC3H1-IT1,RC3H1 Ensembl:ENSG00000236535,Ensembl:ENSG00000135870 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1309464311 Functional Loss SNV dbSNP153 33..33 33 - - - 43501 RMVar_ID_43501 Human_SNP_ID_39297644 A-to-I Human chr1 - 174117443 174117443 174117443 GCCTGGTGGTGTGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCTGGAGGATCGCTTAGCCCAG GCCTGGTGGTGTGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCTGGAGGATCGCTTAGCCCAG T C RABGAP1L-DT Ensembl:ENSG00000227373 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs950150851 Functional Loss SNV dbSNP153 33..33 33 - - - 43502 RMVar_ID_43502 Human_SNP_ID_39304495 A-to-I Human chr1 - 174148466 174148466 174148466 AAAAAAAAAAAAAAAAAATTTTCTCCCATTCTATAGGTTGCCTATTCACTCTGATGGTAGTTTCT AAAAAAAAAAAAAAAAAATTTTCTCCCATTCTGTAGGTTGCCTATTCACTCTGATGGTAGTTTCT T C RABGAP1L-DT Ensembl:ENSG00000227373 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs112367227 Functional Loss SNV dbSNP153 33..33 33 - - - 43503 RMVar_ID_43503 Human_SNP_ID_39310685 A-to-I Human chr1 + 174173224 174173224 174173224 ATGGTCTCGGTTCACCGTAACCTCTGCCTCCCAGGTTCCAGTGATTCTCCTGCCTCAGCCTCCCG ATGGTCTCGGTTCACCGTAACCTCTGCCTCCCGGGTTCCAGTGATTCTCCTGCCTCAGCCTCCCG A G RABGAP1L Ensembl:ENSG00000152061 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1310836420 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107025,RMVar_hsa_circ_137729 43504 RMVar_ID_43504 Human_SNP_ID_39317405 A-to-I Human chr1 + 174198997 174198997 174198997 GGGCGTGGTGGCGCATGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGTAGAGTCGCTTGAA GGGCGTGGTGGCGCATGCCTGTAATCCCAGCTCCTCGGGAGGCTGAGGCAGTAGAGTCGCTTGAA A C RABGAP1L Ensembl:ENSG00000152061 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1359911768 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107025,RMVar_hsa_circ_137729 43505 RMVar_ID_43505 Human_SNP_ID_39322614 A-to-I Human chr1 + 174221066 174221066 174221066 GAAAAGGCCAAGCAGTCTTCTTGTTGATTGTCAAAGTTCCAGTGAGATTTCAGACCATTCGTTTG GAAAAGGCCAAGCAGTCTTCTTGTTGATTGTCGAAGTTCCAGTGAGATTTCAGACCATTCGTTTG A G RABGAP1L Ensembl:ENSG00000152061 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs528581820 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17764257,Human_RBP_ID_27798870 Human_Splice_Rec_159556,Human_Splice_Rec_159557,Human_Splice_Rec_159582,Human_Splice_Rec_159583,Human_Splice_Rec_159622,Human_Splice_Rec_159623,Human_Splice_Rec_159634,Human_Splice_Rec_159635,Human_Splice_Rec_159655 RMVar_hsa_circ_61997,RMVar_hsa_circ_107025,RMVar_hsa_circ_334788,RMVar_hsa_circ_354988,RMVar_hsa_circ_137729,RMVar_hsa_circ_353615,RMVar_hsa_circ_270251,RMVar_hsa_circ_303195,RMVar_hsa_circ_137731,RMVar_hsa_circ_137732,RMVar_hsa_circ_344755,RMVar_hsa_circ_363644,RMVar_hsa_circ_339895,RMVar_hsa_circ_89544,RMVar_hsa_circ_266640,RMVar_hsa_circ_71850,RMVar_hsa_circ_137733,RMVar_hsa_circ_137735,RMVar_hsa_circ_58842,RMVar_hsa_circ_137734 43506 RMVar_ID_43506 Human_SNP_ID_39381609 A-to-I Human chr1 + 174454630 174454630 174454630 TGGAGGGCAGTGGCGCTATCTCTGCTCACTGCAAGCTCGCCTCCCGGGTTCACGCCATTCTCCTG TGGAGGGCAGTGGCGCTATCTCTGCTCACTGCGAGCTCGCCTCCCGGGTTCACGCCATTCTCCTG A G RABGAP1L Ensembl:ENSG00000152061 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1022648394 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10662291 RMVar_hsa_circ_107025,RMVar_hsa_circ_137729,RMVar_hsa_circ_266640,RMVar_hsa_circ_58842,RMVar_hsa_circ_22040,RMVar_hsa_circ_370829,RMVar_hsa_circ_70022,RMVar_hsa_circ_137750,RMVar_hsa_circ_26203,RMVar_hsa_circ_44739,RMVar_hsa_circ_62513,RMVar_hsa_circ_60688,RMVar_hsa_circ_312809,RMVar_hsa_circ_74726 43507 RMVar_ID_43507 Human_SNP_ID_39381648 A-to-I Human chr1 + 174454756 174454756 174454756 TGTTTTTAGTAGAGACTGGGTTCCACCTTGTTAGTCAGGATGGTCTCGATCTCCTGACCTCCTCG TGTTTTTAGTAGAGACTGGGTTCCACCTTGTTGGTCAGGATGGTCTCGATCTCCTGACCTCCTCG A G RABGAP1L Ensembl:ENSG00000152061 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs998997044 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107025,RMVar_hsa_circ_137729,RMVar_hsa_circ_266640,RMVar_hsa_circ_58842,RMVar_hsa_circ_22040,RMVar_hsa_circ_370829,RMVar_hsa_circ_70022,RMVar_hsa_circ_137750,RMVar_hsa_circ_26203,RMVar_hsa_circ_44739,RMVar_hsa_circ_62513,RMVar_hsa_circ_60688,RMVar_hsa_circ_312809,RMVar_hsa_circ_74726 43508 RMVar_ID_43508 Human_SNP_ID_39384278 A-to-I Human chr1 + 174465447 174465447 174465447 GTTTCGAACTGCTGACCTCAGGCGATCCACCCACTTCGGCCTCCCAAAGTGCTGGGATTACAGGC GTTTCGAACTGCTGACCTCAGGCGATCCACCCCCTTCGGCCTCCCAAAGTGCTGGGATTACAGGC A C RABGAP1L Ensembl:ENSG00000152061 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1430807718 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107025,RMVar_hsa_circ_137729,RMVar_hsa_circ_266640,RMVar_hsa_circ_58842,RMVar_hsa_circ_22040,RMVar_hsa_circ_370829,RMVar_hsa_circ_70022,RMVar_hsa_circ_137750,RMVar_hsa_circ_26203,RMVar_hsa_circ_44739,RMVar_hsa_circ_62513,RMVar_hsa_circ_60688,RMVar_hsa_circ_312809,RMVar_hsa_circ_74726 43509 RMVar_ID_43509 Human_SNP_ID_39387298 A-to-I Human chr1 + 174478374 174478374 174478374 CTCACTGTAACCTTGAACTCCTGGGCTCAAGCAATCTTCCTGCCTTAGTCTCCTTAGTAGCTAGT CTCACTGTAACCTTGAACTCCTGGGCTCAAGCCATCTTCCTGCCTTAGTCTCCTTAGTAGCTAGT A C RABGAP1L Ensembl:ENSG00000152061 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs548300518 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18556669 RMVar_hsa_circ_107025,RMVar_hsa_circ_137729,RMVar_hsa_circ_266640,RMVar_hsa_circ_58842,RMVar_hsa_circ_22040,RMVar_hsa_circ_370829,RMVar_hsa_circ_70022,RMVar_hsa_circ_137750,RMVar_hsa_circ_26203,RMVar_hsa_circ_44739,RMVar_hsa_circ_62513,RMVar_hsa_circ_60688,RMVar_hsa_circ_312809,RMVar_hsa_circ_74726 43510 RMVar_ID_43510 Human_SNP_ID_39387299 A-to-I Human chr1 + 174478374 174478374 174478374 CTCACTGTAACCTTGAACTCCTGGGCTCAAGCAATCTTCCTGCCTTAGTCTCCTTAGTAGCTAGT CTCACTGTAACCTTGAACTCCTGGGCTCAAGCTATCTTCCTGCCTTAGTCTCCTTAGTAGCTAGT A T RABGAP1L Ensembl:ENSG00000152061 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs548300518 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18556669 RMVar_hsa_circ_107025,RMVar_hsa_circ_137729,RMVar_hsa_circ_266640,RMVar_hsa_circ_58842,RMVar_hsa_circ_22040,RMVar_hsa_circ_370829,RMVar_hsa_circ_70022,RMVar_hsa_circ_137750,RMVar_hsa_circ_26203,RMVar_hsa_circ_44739,RMVar_hsa_circ_62513,RMVar_hsa_circ_60688,RMVar_hsa_circ_312809,RMVar_hsa_circ_74726 43511 RMVar_ID_43511 Human_SNP_ID_39393712 A-to-I Human chr1 + 174504234 174504234 174504234 AGCTCAAGTGATGTGCCCACCTTGGCCTCCCAAAGTGCTAGGATTACAGGCATGAGCCAGCACGC AGCTCAAGTGATGTGCCCACCTTGGCCTCCCAGAGTGCTAGGATTACAGGCATGAGCCAGCACGC A G RABGAP1L Ensembl:ENSG00000152061 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1004200973 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107025,RMVar_hsa_circ_137729,RMVar_hsa_circ_266640,RMVar_hsa_circ_58842,RMVar_hsa_circ_22040,RMVar_hsa_circ_370829,RMVar_hsa_circ_70022,RMVar_hsa_circ_137750,RMVar_hsa_circ_26203,RMVar_hsa_circ_44739,RMVar_hsa_circ_62513,RMVar_hsa_circ_60688,RMVar_hsa_circ_312809,RMVar_hsa_circ_74726 43512 RMVar_ID_43512 Human_SNP_ID_39393714 A-to-I Human chr1 + 174504241 174504241 174504241 GTGATGTGCCCACCTTGGCCTCCCAAAGTGCTAGGATTACAGGCATGAGCCAGCACGCCTGGCCA GTGATGTGCCCACCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCAGCACGCCTGGCCA A G RABGAP1L Ensembl:ENSG00000152061 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1035385732 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107025,RMVar_hsa_circ_137729,RMVar_hsa_circ_266640,RMVar_hsa_circ_58842,RMVar_hsa_circ_22040,RMVar_hsa_circ_370829,RMVar_hsa_circ_70022,RMVar_hsa_circ_137750,RMVar_hsa_circ_26203,RMVar_hsa_circ_44739,RMVar_hsa_circ_62513,RMVar_hsa_circ_60688,RMVar_hsa_circ_312809,RMVar_hsa_circ_74726 43513 RMVar_ID_43513 Human_SNP_ID_39487057 A-to-I Human chr1 + 174866779 174866779 174866779 ACTAAAAATATAAAAAATGAGCCAGGCTTGGTAGTGCATGCCTGTAGTTCCAGCTACTTGGGAGA ACTAAAAATATAAAAAATGAGCCAGGCTTGGTGGTGCATGCCTGTAGTTCCAGCTACTTGGGAGA A G RABGAP1L Ensembl:ENSG00000152061 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1370986353 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66222 43514 RMVar_ID_43514 Human_SNP_ID_39496575 A-to-I Human chr1 + 174906507 174906507 174906507 AAAATTAGCGGGGTGTGGTGGCAGATGCCTATAATCCCAGCTACTGGGGAGGGTGAGGCAGGAAA AAAATTAGCGGGGTGTGGTGGCAGATGCCTATCATCCCAGCTACTGGGGAGGGTGAGGCAGGAAA A C RABGAP1L Ensembl:ENSG00000152061 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs918894234 Functional Loss SNV dbSNP153 33..33 33 - - - 43515 RMVar_ID_43515 Human_SNP_ID_39523052 A-to-I Human chr1 - 175017140 175017140 175017140 TGAGGCAGGAGAATTGCTTGAACTCGGGAGGCAGAGGTTACAGTGAACCGAGATCACGCCAGTAC TGAGGCAGGAGAATTGCTTGAACTCGGGAGGCGGAGGTTACAGTGAACCGAGATCACGCCAGTAC T C MRPS14 Ensembl:ENSG00000120333 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1382618746 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105382,RMVar_hsa_circ_137772 43516 RMVar_ID_43516 Human_SNP_ID_39755280 A-to-I Human chr1 - 175948991 175948991 175948991 GCCAAGCTAATTTTTTGTATTTTAGTAGAGACAGGATTACACCATATTAGCCAGGATGGTCTCGA GCCAAGCTAATTTTTTGTATTTTAGTAGAGACGGGATTACACCATATTAGCCAGGATGGTCTCGA T C COP1 Ensembl:ENSG00000143207 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs557277250 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_137788,RMVar_hsa_circ_100273,RMVar_hsa_circ_121671,RMVar_hsa_circ_101454,RMVar_hsa_circ_94574,RMVar_hsa_circ_97655,RMVar_hsa_circ_137789,RMVar_hsa_circ_137790,RMVar_hsa_circ_137786,RMVar_hsa_circ_137787 43517 RMVar_ID_43517 Human_SNP_ID_39759940 A-to-I Human chr1 - 175967472 175967472 175967472 GTTTGTTTGTTTGTTTTTTGAGACTGAGTCTCACTGTGTCACCCAGGTTGGAGTGCAGTGGCATA GTTTGTTTGTTTGTTTTTTGAGACTGAGTCTCGCTGTGTCACCCAGGTTGGAGTGCAGTGGCATA T C COP1 Ensembl:ENSG00000143207 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1012007061 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_137788,RMVar_hsa_circ_100273,RMVar_hsa_circ_121671,RMVar_hsa_circ_101454,RMVar_hsa_circ_94574,RMVar_hsa_circ_97655,RMVar_hsa_circ_137789,RMVar_hsa_circ_137790,RMVar_hsa_circ_137786,RMVar_hsa_circ_137787 43518 RMVar_ID_43518 Human_SNP_ID_39760106 A-to-I Human chr1 - 175968050 175968050 175968050 GCCTGGCACCAACATAGTGAAATCCTGTCTCTACTGAAAACACAAAAATTAGCCAGGTGTGTTGG GCCTGGCACCAACATAGTGAAATCCTGTCTCTGCTGAAAACACAAAAATTAGCCAGGTGTGTTGG T C COP1 Ensembl:ENSG00000143207 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1143376 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_137788,RMVar_hsa_circ_100273,RMVar_hsa_circ_121671,RMVar_hsa_circ_101454,RMVar_hsa_circ_94574,RMVar_hsa_circ_97655,RMVar_hsa_circ_137789,RMVar_hsa_circ_137790,RMVar_hsa_circ_137786,RMVar_hsa_circ_137787 43519 RMVar_ID_43519 Human_SNP_ID_39813449 A-to-I Human chr1 - 176172198 176172198 176172198 GTCTCTATAAAAAATTAGCCAGGCGTGTTGGTATGCAGCTGTTGTCCTAGCTTCTTGGGAGGCTG GTCTCTATAAAAAATTAGCCAGGCGTGTTGGTTTGCAGCTGTTGTCCTAGCTTCTTGGGAGGCTG T A COP1 Ensembl:ENSG00000143207 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1199028518 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92233,RMVar_hsa_circ_101454,RMVar_hsa_circ_137786,RMVar_hsa_circ_369407,RMVar_hsa_circ_137798,RMVar_hsa_circ_137797,RMVar_hsa_circ_360284,RMVar_hsa_circ_70261,RMVar_hsa_circ_137800,RMVar_hsa_circ_324333,RMVar_hsa_circ_323117,RMVar_hsa_circ_137818,RMVar_hsa_circ_137817,RMVar_hsa_circ_284025,RMVar_hsa_circ_281730,RMVar_hsa_circ_272595,RMVar_hsa_circ_321690,RMVar_hsa_circ_137828,RMVar_hsa_circ_137837,RMVar_hsa_circ_137838,RMVar_hsa_circ_137842,RMVar_hsa_circ_360403,RMVar_hsa_circ_137839,RMVar_hsa_circ_137841,RMVar_hsa_circ_12586,RMVar_hsa_circ_137843,RMVar_hsa_circ_279586,RMVar_hsa_circ_273278,RMVar_hsa_circ_137844,RMVar_hsa_circ_137848,RMVar_hsa_circ_308398,RMVar_hsa_circ_281475,RMVar_hsa_circ_137847,RMVar_hsa_circ_67121,RMVar_hsa_circ_377370 43520 RMVar_ID_43520 Human_SNP_ID_39815371 A-to-I Human chr1 + 176179441 176179441 176179441 TGACAAGAACAAGCTAGGCTGTTAAGTCAGAGAGGAGTTTGTTAGGCTGGGTGCAGTGGCTCGTG TGACAAGAACAAGCTAGGCTGTTAAGTCAGAGGGGAGTTTGTTAGGCTGGGTGCAGTGGCTCGTG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs566329676 Functional Loss SNV dbSNP153 33..33 33 - - - 43521 RMVar_ID_43521 Human_SNP_ID_39821763 A-to-I Human chr1 - 176204841 176204841 176204841 TCACTGCCACCCCCGCCTCCCGGGTTCAAGCAATTCTCCAGCCTCAGCCTCCCGAGTAGTAGCTG TCACTGCCACCCCCGCCTCCCGGGTTCAAGCAGTTCTCCAGCCTCAGCCTCCCGAGTAGTAGCTG T C COP1 Ensembl:ENSG00000143207 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs374099230 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107818,RMVar_hsa_circ_137851 43522 RMVar_ID_43522 Human_SNP_ID_39927529 A-to-I Human chr1 + 176657971 176657971 176657971 TTCCATTTAGAGTCCATCTCCAGCATTAATATAATCAACTACTATTGAATAAGCACTTGATAATA TTCCATTTAGAGTCCATCTCCAGCATTAATATGATCAACTACTATTGAATAAGCACTTGATAATA A G PAPPA2 Ensembl:ENSG00000116183 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1377894513 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111541,RMVar_hsa_circ_137852,RMVar_hsa_circ_15157 43523 RMVar_ID_43523 Human_SNP_ID_40067543 A-to-I Human chr1 + 177263001 177263001 177263001 AGGCATGGAATAGACAAAGAGTTGGATTTAACAAAGATGTGTGTATATACGTGGCGAAAGATAAA AGGCATGGAATAGACAAAGAGTTGGATTTAACGAAGATGTGTGTATATACGTGGCGAAAGATAAA A G BRINP2 Ensembl:ENSG00000198797 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs889895311 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267802 43524 RMVar_ID_43524 Human_SNP_ID_40255741 A-to-I Human chr1 - 178035985 178035985 178035985 AGGCTCAAGCAGTTCTCCCACCCCAGTCTCCCAAGTAGCTGAGACCACAGGCACATGCCACCATT AGGCTCAAGCAGTTCTCCCACCCCAGTCTCCCGAGTAGCTGAGACCACAGGCACATGCCACCATT T C CRYZL2P,CRYZL2P-SEC16B Ensembl:ENSG00000242193,Ensembl:ENSG00000254154 Pseudogene,lincRNA intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1408619707 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10312 43525 RMVar_ID_43525 Human_SNP_ID_40255746 A-to-I Human chr1 - 178035998 178035998 178035998 ACCTTGACCTCCCAGGCTCAAGCAGTTCTCCCACCCCAGTCTCCCAAGTAGCTGAGACCACAGGC ACCTTGACCTCCCAGGCTCAAGCAGTTCTCCCTCCCCAGTCTCCCAAGTAGCTGAGACCACAGGC T A CRYZL2P,CRYZL2P-SEC16B Ensembl:ENSG00000242193,Ensembl:ENSG00000254154 Pseudogene,lincRNA intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1254230920 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10312 43526 RMVar_ID_43526 Human_SNP_ID_40273752 A-to-I Human chr1 + 178110727 178110727 178110727 CTCATGCCTCAGCCTCCTGAGTAGCTGGGATTAAGGCACACACTACTATGCCTGGCTAATTTTTT CTCATGCCTCAGCCTCCTGAGTAGCTGGGATTGAGGCACACACTACTATGCCTGGCTAATTTTTT A G RASAL2 Ensembl:ENSG00000075391 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1229396758 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84755,RMVar_hsa_circ_137890 43527 RMVar_ID_43527 Human_SNP_ID_40274551 A-to-I Human chr1 + 178113603 178113603 178113603 CAGAGTCTTGCTGTATTGCCCAGGCTGGTCTGAAACTCCTGGCCTCAAGCAATCCCCCAACCTTC CAGAGTCTTGCTGTATTGCCCAGGCTGGTCTGCAACTCCTGGCCTCAAGCAATCCCCCAACCTTC A C RASAL2 Ensembl:ENSG00000075391 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1352172079 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84755,RMVar_hsa_circ_137890 43528 RMVar_ID_43528 Human_SNP_ID_40282678 A-to-I Human chr1 + 178148679 178148679 178148679 GTTGCCCAGGCTAGTCTCAAATTCCCAAGCTCAAGCAATACACTACCTCAGCCTCCCAAAGTGTT GTTGCCCAGGCTAGTCTCAAATTCCCAAGCTCGAGCAATACACTACCTCAGCCTCCCAAAGTGTT A G RASAL2 Ensembl:ENSG00000075391 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1308999700 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84755,RMVar_hsa_circ_137890 43529 RMVar_ID_43529 Human_SNP_ID_40283278 A-to-I Human chr1 + 178151346 178151346 178151346 AGAATTGCTTGAACCCAGTAAACGGAGGTTGCAGTGAGCCGAGATCGCACCACTTCACTCTAGCC AGAATTGCTTGAACCCAGTAAACGGAGGTTGCTGTGAGCCGAGATCGCACCACTTCACTCTAGCC A T RASAL2 Ensembl:ENSG00000075391 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749289994 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84755,RMVar_hsa_circ_137890 43530 RMVar_ID_43530 Human_SNP_ID_40287657 A-to-I Human chr1 + 178169159 178169159 178169159 AATGTACCATTTGTCAATTTTCTGACATTTTTATGACTACCTACTTACCTAGTACACGAAAAAAT AATGTACCATTTGTCAATTTTCTGACATTTTTGTGACTACCTACTTACCTAGTACACGAAAAAAT A G RASAL2 Ensembl:ENSG00000075391 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1410452394 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84755,RMVar_hsa_circ_137890 43531 RMVar_ID_43531 Human_SNP_ID_40290259 A-to-I Human chr1 + 178180636 178180636 178180636 TTTCAGTGAGCTGCGATCACAGCACTGCATTCAAGCCTGGGTGATGGAGCGAGACTGTCTCACAC TTTCAGTGAGCTGCGATCACAGCACTGCATTCGAGCCTGGGTGATGGAGCGAGACTGTCTCACAC A G RASAL2 Ensembl:ENSG00000075391 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1319180269 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84755,RMVar_hsa_circ_137890 43532 RMVar_ID_43532 Human_SNP_ID_40295830 A-to-I Human chr1 + 178205279 178205279 178205279 TGCCTGCCTTGGCCTCCCAAAGTGCTGTGATTACAGGTGTGAGGCACTGTGCCCAGCCCAGAAAA TGCCTGCCTTGGCCTCCCAAAGTGCTGTGATTGCAGGTGTGAGGCACTGTGCCCAGCCCAGAAAA A G RASAL2 Ensembl:ENSG00000075391 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1261305033 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84755,RMVar_hsa_circ_137890 43533 RMVar_ID_43533 Human_SNP_ID_40297908 A-to-I Human chr1 + 178213976 178213976 178213976 AATTCAGGAAGAGGCTGGACGTGGTAGCTCATACCTGTAATTCTAACACTTTGGGAGACTCCCAA AATTCAGGAAGAGGCTGGACGTGGTAGCTCATGCCTGTAATTCTAACACTTTGGGAGACTCCCAA A G RASAL2 Ensembl:ENSG00000075391 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1347323388 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84755,RMVar_hsa_circ_137890 43534 RMVar_ID_43534 Human_SNP_ID_40358339 A-to-I Human chr1 - 178481076 178481076 178481076 CATGCTTGCCAGGAGTGGAGGGGGGACTGGAGAGCTTTCAGTACATTTTGCTATTGAAAGAACAA CATGCTTGCCAGGAGTGGAGGGGGGACTGGAGCGCTTTCAGTACATTTTGCTATTGAAAGAACAA T G CLEC20A Ensembl:ENSG00000188585 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs574018263 Functional Loss SNV dbSNP153 33..33 33 - - - 43535 RMVar_ID_43535 Human_SNP_ID_40358842 A-to-I Human chr1 + 178483245 178483245 178483245 CTCAGATGTTGGGCCTCCGTGGCAGCAGCTGTATCTCTTCTATCAGTGCCACTCCCTACACTGGC CTCAGATGTTGGGCCTCCGTGGCAGCAGCTGTGTCTCTTCTATCAGTGCCACTCCCTACACTGGC A G RASAL2 Ensembl:ENSG00000075391 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1325372411 Functional Loss SNV dbSNP153 33..33 33 - - - 43536 RMVar_ID_43536 Human_SNP_ID_40495697 A-to-I Human chr1 + 179049572 179049572 179049572 CAAAAGTTTTTTGTTTTTTGAGACAGAGCCTCACTCTGTTGCCCAGGCTGGAGTGCAGTGGCACA CAAAAGTTTTTTGTTTTTTGAGACAGAGCCTCGCTCTGTTGCCCAGGCTGGAGTGCAGTGGCACA A G FAM20B Ensembl:ENSG00000116199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs906041640 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77766,RMVar_hsa_circ_137939,RMVar_hsa_circ_281213,RMVar_hsa_circ_317293,RMVar_hsa_circ_366437,RMVar_hsa_circ_137937,RMVar_hsa_circ_302846,RMVar_hsa_circ_137940,RMVar_hsa_circ_137938 43537 RMVar_ID_43537 Human_SNP_ID_40496244 A-to-I Human chr1 + 179051746 179051746 179051746 TTGGCTTACTGCAACCTCGACGTCCTGGGTTCAAACAGTTATCCTGCCTCAGCCTACCGAGTAGC TTGGCTTACTGCAACCTCGACGTCCTGGGTTCCAACAGTTATCCTGCCTCAGCCTACCGAGTAGC A C FAM20B Ensembl:ENSG00000116199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1314497273 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77766,RMVar_hsa_circ_137939,RMVar_hsa_circ_281213,RMVar_hsa_circ_366437,RMVar_hsa_circ_137937,RMVar_hsa_circ_302846,RMVar_hsa_circ_137940,RMVar_hsa_circ_281051,RMVar_hsa_circ_314657,RMVar_hsa_circ_137938,RMVar_hsa_circ_311589,RMVar_hsa_circ_137941 43538 RMVar_ID_43538 Human_SNP_ID_40499827 A-to-I Human chr1 + 179067493 179067493 179067493 CGGGCATGGTGGCAGGCACCAGTATTCCAGCTACTTAGGAGGTTGAGACAGGAGAATTGCTTGAA CGGGCATGGTGGCAGGCACCAGTATTCCAGCTGCTTAGGAGGTTGAGACAGGAGAATTGCTTGAA A G FAM20B Ensembl:ENSG00000116199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1176180634 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_96104 RMVar_hsa_circ_110032,RMVar_hsa_circ_137946 43539 RMVar_ID_43539 Human_SNP_ID_40500757 A-to-I Human chr1 + 179071189 179071188 179071189 GTGGTGGCGGGTGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATGGCGTGAACCCG GTGGTGGCGGGTGCCTGTAGTCCCAGCTACTC_GGAGGCTGAGGCAGGAGAATGGCGTGAACCCG CA C FAM20B Ensembl:ENSG00000116199 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1426226270 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_96105 RMVar_hsa_circ_110032,RMVar_hsa_circ_137946 43540 RMVar_ID_43540 Human_SNP_ID_40500760 A-to-I Human chr1 + 179071189 179071189 179071189 GTGGTGGCGGGTGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATGGCGTGAACCCG GTGGTGGCGGGTGCCTGTAGTCCCAGCTACTCCGGAGGCTGAGGCAGGAGAATGGCGTGAACCCG A C FAM20B Ensembl:ENSG00000116199 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs894561270 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_96105 RMVar_hsa_circ_110032,RMVar_hsa_circ_137946 43541 RMVar_ID_43541 Human_SNP_ID_40501311 A-to-I Human chr1 + 179073415 179073415 179073415 TTGGCTTACTGCAACCTCCGTCTCCCAGGTTCAAGCGATTCTCTTGCCTCAGCCTCCAGAGTAGC TTGGCTTACTGCAACCTCCGTCTCCCAGGTTCGAGCGATTCTCTTGCCTCAGCCTCCAGAGTAGC A G FAM20B Ensembl:ENSG00000116199 Protein coding 3'UTR GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1040616440 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110032,RMVar_hsa_circ_137946 43542 RMVar_ID_43542 Human_SNP_ID_40501341 A-to-I Human chr1 + 179073562 179073562 179073562 CCAGGTTGATCTTGGACTCCTGACCCCAGGTGATCCACCTGCCTCAGCCTTCCAAAGTGCTGGGA CCAGGTTGATCTTGGACTCCTGACCCCAGGTGTTCCACCTGCCTCAGCCTTCCAAAGTGCTGGGA A T FAM20B Ensembl:ENSG00000116199 Protein coding 3'UTR GSE100210;GSE99789;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,29796672,32596459 RNA-Seq:(High) rs1171683080 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557388 RMVar_hsa_circ_110032,RMVar_hsa_circ_137946 43543 RMVar_ID_43543 Human_SNP_ID_40501347 A-to-I Human chr1 + 179073583 179073583 179073583 GACCCCAGGTGATCCACCTGCCTCAGCCTTCCAAAGTGCTGGGATTACAGGCATGAGCCACCGTG GACCCCAGGTGATCCACCTGCCTCAGCCTTCCGAAGTGCTGGGATTACAGGCATGAGCCACCGTG A G FAM20B Ensembl:ENSG00000116199 Protein coding 3'UTR GSE38233;GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,32596459 RNA-Seq:(High) rs1196731391 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557388 RMVar_hsa_circ_110032,RMVar_hsa_circ_137946 43544 RMVar_ID_43544 Human_SNP_ID_40501352 A-to-I Human chr1 + 179073606 179073606 179073606 CAGCCTTCCAAAGTGCTGGGATTACAGGCATGAGCCACCGTGGCCGGCCAAGATTTTAAGCCTTC CAGCCTTCCAAAGTGCTGGGATTACAGGCATGTGCCACCGTGGCCGGCCAAGATTTTAAGCCTTC A T FAM20B Ensembl:ENSG00000116199 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947955039 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557388,Human_RBP_ID_26386742 Human_miRNA_ID_675776 RMVar_hsa_circ_110032,RMVar_hsa_circ_137946 43545 RMVar_ID_43545 Human_SNP_ID_40501614 A-to-I Human chr1 + 179074957 179074957 179074957 TCATGCCTGTCATCCCAGCATTTGGGAGGCTGAGGCAGGCAGATCACCTGAGGCCAGGAGTTCGA TCATGCCTGTCATCCCAGCATTTGGGAGGCTGGGGCAGGCAGATCACCTGAGGCCAGGAGTTCGA A G FAM20B Ensembl:ENSG00000116199 Protein coding 3'UTR GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,29796672,31158229,32596459 RNA-Seq:(High) rs1341231825 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110032,RMVar_hsa_circ_137946 43546 RMVar_ID_43546 Human_SNP_ID_40501618 A-to-I Human chr1 + 179074965 179074965 179074965 GTCATCCCAGCATTTGGGAGGCTGAGGCAGGCAGATCACCTGAGGCCAGGAGTTCGAGACCAGCC GTCATCCCAGCATTTGGGAGGCTGAGGCAGGCGGATCACCTGAGGCCAGGAGTTCGAGACCAGCC A G FAM20B Ensembl:ENSG00000116199 Protein coding 3'UTR GSE47997;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,29129909,29796672,31158229,31158229,32596459,32596459 RNA-Seq:(High) rs1193651609 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4010086 RMVar_hsa_circ_110032,RMVar_hsa_circ_137946 43547 RMVar_ID_43547 Human_SNP_ID_40501620 A-to-I Human chr1 + 179074980 179074980 179074980 GGGAGGCTGAGGCAGGCAGATCACCTGAGGCCAGGAGTTCGAGACCAGCCTGGCTGGCTAGCATG GGGAGGCTGAGGCAGGCAGATCACCTGAGGCCTGGAGTTCGAGACCAGCCTGGCTGGCTAGCATG A T FAM20B Ensembl:ENSG00000116199 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs575209667 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110032,RMVar_hsa_circ_137946 43548 RMVar_ID_43548 Human_SNP_ID_40501633 A-to-I Human chr1 + 179075030 179075030 179075030 TGGCTGGCTAGCATGGTGAGACCGTCTCTACTAAAAATGCAAAAATTAACAGGGCACGGTGGCAT TGGCTGGCTAGCATGGTGAGACCGTCTCTACTGAAAATGCAAAAATTAACAGGGCACGGTGGCAT A G FAM20B Ensembl:ENSG00000116199 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1255407376 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5720658 RMVar_hsa_circ_110032,RMVar_hsa_circ_137946 43549 RMVar_ID_43549 Human_SNP_ID_40501636 A-to-I Human chr1 + 179075048 179075047 179075048 AGACCGTCTCTACTAAAAATGCAAAAATTAACAGGGCACGGTGGCATGCGCCTGTAGTCCCAGCT AGACCGTCTCTACTAAAAATGCAAAAATTAAC_GGGCACGGTGGCATGCGCCTGTAGTCCCAGCT CA C FAM20B Ensembl:ENSG00000116199 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1198804713 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_110032,RMVar_hsa_circ_137946 43550 RMVar_ID_43550 Human_SNP_ID_40501637 A-to-I Human chr1 + 179075048 179075047 179075049 AGACCGTCTCTACTAAAAATGCAAAAATTAACAGGGCACGGTGGCATGCGCCTGTAGTCCCAGCT AGACCGTCTCTACTAAAAATGCAAAAATTAAC__GGCACGGTGGCATGCGCCTGTAGTCCCAGCT CAG C FAM20B Ensembl:ENSG00000116199 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1553208189 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_110032,RMVar_hsa_circ_137946 43551 RMVar_ID_43551 Human_SNP_ID_40501638 A-to-I Human chr1 + 179075048 179075048 179075048 AGACCGTCTCTACTAAAAATGCAAAAATTAACAGGGCACGGTGGCATGCGCCTGTAGTCCCAGCT AGACCGTCTCTACTAAAAATGCAAAAATTAACGGGGCACGGTGGCATGCGCCTGTAGTCCCAGCT A G FAM20B Ensembl:ENSG00000116199 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202400493 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110032,RMVar_hsa_circ_137946 43552 RMVar_ID_43552 Human_SNP_ID_40501652 A-to-I Human chr1 + 179075071 179075071 179075071 AAAATTAACAGGGCACGGTGGCATGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTAACAGGGCACGGTGGCATGCGCCTGTGGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA A G FAM20B Ensembl:ENSG00000116199 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,29129909,29796672,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs1327964172 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110032,RMVar_hsa_circ_137946 43553 RMVar_ID_43553 Human_SNP_ID_40501654 A-to-I Human chr1 + 179075077 179075077 179075077 AACAGGGCACGGTGGCATGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACT AACAGGGCACGGTGGCATGCGCCTGTAGTCCCGGCTACTCGGGAGGCTGAGGCAGGAGAATCACT A G FAM20B Ensembl:ENSG00000116199 Protein coding 3'UTR GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1368903913 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110032,RMVar_hsa_circ_137946 43554 RMVar_ID_43554 Human_SNP_ID_40501655 A-to-I Human chr1 + 179075081 179075081 179075081 GGGCACGGTGGCATGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAA GGGCACGGTGGCATGCGCCTGTAGTCCCAGCTGCTCGGGAGGCTGAGGCAGGAGAATCACTTGAA A G FAM20B Ensembl:ENSG00000116199 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs1386092913 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24611652 RMVar_hsa_circ_110032,RMVar_hsa_circ_137946 43555 RMVar_ID_43555 Human_SNP_ID_40501660 A-to-I Human chr1 + 179075117 179075117 179075117 GGGAGGCTGAGGCAGGAGAATCACTTGAATCCAGGAGGCGAAGGTTGCAGTGAGCTGAGATTGTG GGGAGGCTGAGGCAGGAGAATCACTTGAATCCGGGAGGCGAAGGTTGCAGTGAGCTGAGATTGTG A G FAM20B Ensembl:ENSG00000116199 Protein coding 3'UTR GSE47997;GSE38233;GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,24183664,29129909,31158229,32596459 RNA-Seq:(High) rs1225045270 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110032,RMVar_hsa_circ_137946 43556 RMVar_ID_43556 Human_SNP_ID_40501672 A-to-I Human chr1 + 179075157 179075157 179075157 AAGGTTGCAGTGAGCTGAGATTGTGCTGCTGCACTCCAGCCTGGGAGACAGAGCGAGACTCTGTC AAGGTTGCAGTGAGCTGAGATTGTGCTGCTGCGCTCCAGCCTGGGAGACAGAGCGAGACTCTGTC A G FAM20B Ensembl:ENSG00000116199 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1228775199 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110032,RMVar_hsa_circ_137946 43557 RMVar_ID_43557 Human_SNP_ID_40502170 A-to-I Human chr1 + 179077211 179077211 179077211 TGTAATCCCAGCTACTCTGGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGGGAGGCGGAGAGC TGTAATCCCAGCTACTCTGGGGAGGCTGAGGCGGGAGAATCGCTTGAACCCGGGAGGCGGAGAGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs553890923 Functional Loss SNV dbSNP153 33..33 33 - - - 43558 RMVar_ID_43558 Human_SNP_ID_40502551 A-to-I Human chr1 + 179078601 179078601 179078601 CACCACGCCCGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCTCCATATTGGCCGGGCTGA CACCACGCCCGGCTAATTTTTGTATTTTTAGTGGAGACGGGGTTTCTCCATATTGGCCGGGCTGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs936955804 Functional Loss SNV dbSNP153 33..33 33 - - - 43559 RMVar_ID_43559 Human_SNP_ID_40502654 A-to-I Human chr1 + 179078992 179078992 179078992 GTGATCCTCCTCCCTCAGCCTCTCAAGTAGCTAGGATTATAGGCGCGCACCACCACACGCAGCTT GTGATCCTCCTCCCTCAGCCTCTCAAGTAGCTGGGATTATAGGCGCGCACCACCACACGCAGCTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1557884844 Functional Loss SNV dbSNP153 33..33 33 - - - 43560 RMVar_ID_43560 Human_SNP_ID_40502897 A-to-I Human chr1 + 179079721 179079721 179079721 GCGGGGGCGTGGTGGTGAACGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGGGGAAGAATCGCT GCGGGGGCGTGGTGGTGAACGCCTGTAATCCCGGCTACTTGGGAGGCTGAGGGGGAAGAATCGCT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs562953793 Functional Loss SNV dbSNP153 33..33 33 - - - 43561 RMVar_ID_43561 Human_SNP_ID_40504275 A-to-I Human chr1 + 179083668 179083668 179083668 CCTGACCTTGTGATTTGCCTGCCTTGGCCTCCAAGAGTGCTGTGATTACAGGCGTGAGCCACTGT CCTGACCTTGTGATTTGCCTGCCTTGGCCTCCGAGAGTGCTGTGATTACAGGCGTGAGCCACTGT A G TOR3A Ensembl:ENSG00000186283 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs894414471 Functional Loss SNV dbSNP153 33..33 33 - - - 43562 RMVar_ID_43562 Human_SNP_ID_40510923 A-to-I Human chr1 - 179108201 179108201 179108201 GGACAGTCCACATCAGAAACACAGGAAGGAGGAAAGAAGGCAGCTCTGGGCGCAGTGCCCATCAG GGACAGTCCACATCAGAAACACAGGAAGGAGGGAAGAAGGCAGCTCTGGGCGCAGTGCCCATCAG T C ABL2 Ensembl:ENSG00000143322 Protein coding CDS GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1402651170 Functional Loss SNV dbSNP153 33..33 33 - - - 43563 RMVar_ID_43563 Human_SNP_ID_40510929 A-to-I Human chr1 - 179108211 179108211 179108211 CCTAACTGCAGGACAGTCCACATCAGAAACACAGGAAGGAGGAAAGAAGGCAGCTCTGGGCGCAG CCTAACTGCAGGACAGTCCACATCAGAAACACGGGAAGGAGGAAAGAAGGCAGCTCTGGGCGCAG T C ABL2 Ensembl:ENSG00000143322 Protein coding CDS GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs758949211 Functional Loss SNV dbSNP153 33..33 33 - - - 43564 RMVar_ID_43564 Human_SNP_ID_40512485 A-to-I Human chr1 - 179112957 179112957 179112957 CTGAGGTCAGGGGTTCGAGACCAGCATGGCCAACATGGCGAAACCCCTGTCTACTAAAAATACAA CTGAGGTCAGGGGTTCGAGACCAGCATGGCCAGCATGGCGAAACCCCTGTCTACTAAAAATACAA T C ABL2 Ensembl:ENSG00000143322 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1319593392 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7271,RMVar_hsa_circ_43641,RMVar_hsa_circ_308320,RMVar_hsa_circ_364889,RMVar_hsa_circ_50699,RMVar_hsa_circ_273320,RMVar_hsa_circ_315087,RMVar_hsa_circ_337138,RMVar_hsa_circ_84467,RMVar_hsa_circ_44890,RMVar_hsa_circ_137954,RMVar_hsa_circ_137951,RMVar_hsa_circ_137950,RMVar_hsa_circ_89129,RMVar_hsa_circ_297448,RMVar_hsa_circ_373438,RMVar_hsa_circ_367757,RMVar_hsa_circ_320300,RMVar_hsa_circ_284843,RMVar_hsa_circ_137957,RMVar_hsa_circ_137959,RMVar_hsa_circ_137960,RMVar_hsa_circ_137961,RMVar_hsa_circ_137958,RMVar_hsa_circ_137956 43565 RMVar_ID_43565 Human_SNP_ID_40522034 A-to-I Human chr1 - 179148837 179148837 179148837 GGAGTGCAGTGGCATGATCTCGGCGTACTGCAACCTCTGCCTCCCAGGTTCAAGCAATTCTACTG GGAGTGCAGTGGCATGATCTCGGCGTACTGCAGCCTCTGCCTCCCAGGTTCAAGCAATTCTACTG T C ABL2 Ensembl:ENSG00000143322 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1336481459 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77843,RMVar_hsa_circ_137967,RMVar_hsa_circ_103408,RMVar_hsa_circ_137976 43566 RMVar_ID_43566 Human_SNP_ID_40530948 A-to-I Human chr1 - 179186812 179186812 179186812 GAATTGCTTGAACCTGGGAGGTGGAGGTTGCAATGAGCCTAGGTTGCACCATTGCACTCCAGCCT GAATTGCTTGAACCTGGGAGGTGGAGGTTGCAGTGAGCCTAGGTTGCACCATTGCACTCCAGCCT T C ABL2 Ensembl:ENSG00000143322 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1446533222 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77843,RMVar_hsa_circ_137967,RMVar_hsa_circ_103408,RMVar_hsa_circ_137976 43567 RMVar_ID_43567 Human_SNP_ID_40531261 A-to-I Human chr1 - 179188316 179188316 179188316 GCTCATCTCCAACTCCTGCCCTTAGGTGATCTACCTAGCTTGGCTTCCCACAGTGCTGGGATTAC GCTCATCTCCAACTCCTGCCCTTAGGTGATCTGCCTAGCTTGGCTTCCCACAGTGCTGGGATTAC T C ABL2 Ensembl:ENSG00000143322 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs939095845 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77843,RMVar_hsa_circ_137967,RMVar_hsa_circ_103408,RMVar_hsa_circ_137976 43568 RMVar_ID_43568 Human_SNP_ID_40531323 A-to-I Human chr1 - 179188463 179188463 179188463 GGCTTACTGCAACCTCTACCTCCCGCGTTCAAACAATTCTCCTGCCTCAGCCCCCTGAGTAGCTG GGCTTACTGCAACCTCTACCTCCCGCGTTCAAGCAATTCTCCTGCCTCAGCCCCCTGAGTAGCTG T C ABL2 Ensembl:ENSG00000143322 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968336051 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77843,RMVar_hsa_circ_137967,RMVar_hsa_circ_103408,RMVar_hsa_circ_137976 43569 RMVar_ID_43569 Human_SNP_ID_40534163 A-to-I Human chr1 - 179199732 179199730 179199733 GAGAGAATCTGTCTCAAAAAAAAAAAAAAAAAAGGAAAAAGTGTATGGGTTTTGGAACTAGATAG GAGAGAATCTGTCTCAAAAAAAAAAAAAAAA___GAAAAAGTGTATGGGTTTTGGAACTAGATAG CCTT C ABL2 Ensembl:ENSG00000143322 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs968836619 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_24611908 RMVar_hsa_circ_77843,RMVar_hsa_circ_137967,RMVar_hsa_circ_103408,RMVar_hsa_circ_137976 43570 RMVar_ID_43570 Human_SNP_ID_40538495 A-to-I Human chr1 - 179217542 179217542 179217542 GGCTCACTGCAACCTCCACCCACTGGGTTCAAACGGTTCTCCTGCCTCAGCCTCCCGAGTAGCTG GGCTCACTGCAACCTCCACCCACTGGGTTCAAGCGGTTCTCCTGCCTCAGCCTCCCGAGTAGCTG T C ABL2 Ensembl:ENSG00000143322 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1356921088 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77843,RMVar_hsa_circ_137967,RMVar_hsa_circ_103408,RMVar_hsa_circ_137976 43571 RMVar_ID_43571 Human_SNP_ID_40539865 A-to-I Human chr1 - 179223294 179223294 179223294 TTCCTGACTCAGCCTTCTGGGTAGCTGGGACTATAGGTGCGTGCTACCATGCCTGGCTAATTTTT TTCCTGACTCAGCCTTCTGGGTAGCTGGGACTGTAGGTGCGTGCTACCATGCCTGGCTAATTTTT T C ABL2 Ensembl:ENSG00000143322 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1326649049 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77843,RMVar_hsa_circ_137967,RMVar_hsa_circ_103408,RMVar_hsa_circ_137976 43572 RMVar_ID_43572 Human_SNP_ID_40539885 A-to-I Human chr1 - 179223369 179223369 179223369 TTGCTCTGTTGCCTAGGCTGGAGTGCTGTGGCATGATGATAGCTCACTGCAGCCTCAAACTCCTG TTGCTCTGTTGCCTAGGCTGGAGTGCTGTGGCGTGATGATAGCTCACTGCAGCCTCAAACTCCTG T C ABL2 Ensembl:ENSG00000143322 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956885836 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77843,RMVar_hsa_circ_137967,RMVar_hsa_circ_103408,RMVar_hsa_circ_137976 43573 RMVar_ID_43573 Human_SNP_ID_40558980 A-to-I Human chr1 + 179297587 179297587 179297587 TAGAATTCCTGACCTTGTGATCCACCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG TAGAATTCCTGACCTTGTGATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG A G SOAT1 Ensembl:ENSG00000057252 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1488270901 Functional Loss SNV dbSNP153 33..33 33 - - - 43574 RMVar_ID_43574 Human_SNP_ID_40559097 A-to-I Human chr1 + 179297954 179297954 179297954 AATCCAGGAGGCGGAGGTTGCGGTGAGCTGAGATCGTGCCATTGCACTCCAGTCTGACCAACAAG AATCCAGGAGGCGGAGGTTGCGGTGAGCTGAGTTCGTGCCATTGCACTCCAGTCTGACCAACAAG A T SOAT1 Ensembl:ENSG00000057252 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1419628826 Functional Loss SNV dbSNP153 33..33 33 - - - 43575 RMVar_ID_43575 Human_SNP_ID_40563624 A-to-I Human chr1 + 179316593 179316593 179316593 AATTTTGTATTTTTAGTAGACAGGGCTTCTCCATGTTGGTCAGGCTGGTCTCAAACTGCCGACCT AATTTTGTATTTTTAGTAGACAGGGCTTCTCCCTGTTGGTCAGGCTGGTCTCAAACTGCCGACCT A C SOAT1 Ensembl:ENSG00000057252 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1454285462 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63239,RMVar_hsa_circ_319781,RMVar_hsa_circ_366618,RMVar_hsa_circ_358117,RMVar_hsa_circ_264822,RMVar_hsa_circ_294991,RMVar_hsa_circ_67989,RMVar_hsa_circ_137979,RMVar_hsa_circ_137980 43576 RMVar_ID_43576 Human_SNP_ID_40563625 A-to-I Human chr1 + 179316593 179316593 179316593 AATTTTGTATTTTTAGTAGACAGGGCTTCTCCATGTTGGTCAGGCTGGTCTCAAACTGCCGACCT AATTTTGTATTTTTAGTAGACAGGGCTTCTCCGTGTTGGTCAGGCTGGTCTCAAACTGCCGACCT A G SOAT1 Ensembl:ENSG00000057252 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1454285462 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63239,RMVar_hsa_circ_319781,RMVar_hsa_circ_366618,RMVar_hsa_circ_358117,RMVar_hsa_circ_264822,RMVar_hsa_circ_294991,RMVar_hsa_circ_67989,RMVar_hsa_circ_137979,RMVar_hsa_circ_137980 43577 RMVar_ID_43577 Human_SNP_ID_40570673 A-to-I Human chr1 + 179344540 179344540 179344540 GGGATTACAGGTGCCCACCACTGCGCCTGGCTAATTTTTGTATTTTTAGTACAGATGGGGTTTCA GGGATTACAGGTGCCCACCACTGCGCCTGGCTGATTTTTGTATTTTTAGTACAGATGGGGTTTCA A G SOAT1 Ensembl:ENSG00000057252 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1260791528 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11080,RMVar_hsa_circ_63239,RMVar_hsa_circ_366618,RMVar_hsa_circ_264822,RMVar_hsa_circ_67989,RMVar_hsa_circ_311460,RMVar_hsa_circ_352097,RMVar_hsa_circ_308675,RMVar_hsa_circ_29457,RMVar_hsa_circ_361842,RMVar_hsa_circ_302731,RMVar_hsa_circ_21096,RMVar_hsa_circ_69311,RMVar_hsa_circ_137989,RMVar_hsa_circ_281294,RMVar_hsa_circ_52659,RMVar_hsa_circ_137990,RMVar_hsa_circ_322759,RMVar_hsa_circ_333300,RMVar_hsa_circ_285831,RMVar_hsa_circ_137998,RMVar_hsa_circ_137999,RMVar_hsa_circ_137997,RMVar_hsa_circ_344008,RMVar_hsa_circ_53716,RMVar_hsa_circ_350103 43578 RMVar_ID_43578 Human_SNP_ID_40573803 A-to-I Human chr1 + 179356575 179356575 179356575 TGGGGTTTTACCATGTTGCTCAGGCTGGTCTCAAACTCCTGGAGTCAAGGGATCTATTTGCCTCA TGGGGTTTTACCATGTTGCTCAGGCTGGTCTCGAACTCCTGGAGTCAAGGGATCTATTTGCCTCA A G SOAT1 Ensembl:ENSG00000057252 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1457607224 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5721511,Human_RBP_ID_10676282,Human_RBP_ID_26388928 RMVar_hsa_circ_264822 43579 RMVar_ID_43579 Human_SNP_ID_40573810 A-to-I Human chr1 + 179356607 179356607 179356607 AAACTCCTGGAGTCAAGGGATCTATTTGCCTCAGCCTCTCAAAGTGCTGGGATTACAGGTGTGAG AAACTCCTGGAGTCAAGGGATCTATTTGCCTCCGCCTCTCAAAGTGCTGGGATTACAGGTGTGAG A C SOAT1 Ensembl:ENSG00000057252 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017286072 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19152329 RMVar_hsa_circ_264822 43580 RMVar_ID_43580 Human_SNP_ID_40573857 A-to-I Human chr1 + 179356813 179356813 179356813 CTCCTGGACTCAAATAGTGCTCTGGAGTACCTAGAACTACAAGTGCCTACCACCACACCCAGCTA CTCCTGGACTCAAATAGTGCTCTGGAGTACCTGGAACTACAAGTGCCTACCACCACACCCAGCTA A G SOAT1 Ensembl:ENSG00000057252 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1478975700 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_334407,Human_RBP_ID_10676283 RMVar_hsa_circ_264822 43581 RMVar_ID_43581 Human_SNP_ID_40573901 A-to-I Human chr1 + 179356923 179356923 179356923 GTTGCCCAGGCTGGTCTCAAACTCTTCACCTCAAGCAAAACTCCCACTGCAGAAAGCTTTGGGAT GTTGCCCAGGCTGGTCTCAAACTCTTCACCTCCAGCAAAACTCCCACTGCAGAAAGCTTTGGGAT A C SOAT1 Ensembl:ENSG00000057252 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs957699049 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26386751 RMVar_hsa_circ_264822 43582 RMVar_ID_43582 Human_SNP_ID_40574113 A-to-I Human chr1 + 179357882 179357882 179357882 GTGATCACACCACTTAATTCCTCAAAACATTTATGTCCCAGTTCCCTCCATTTCAGAGCCATGGG GTGATCACACCACTTAATTCCTCAAAACATTTGTGTCCCAGTTCCCTCCATTTCAGAGCCATGGG A G SOAT1 Ensembl:ENSG00000057252 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs45471092 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_334413,Human_RBP_ID_4010487,Human_RBP_ID_17557393,Human_RBP_ID_23303032 Human_miRNA_ID_880048 GWAS_ID_4994,GWAS_ID_4995,GWAS_ID_4996,GWAS_ID_4997,GWAS_ID_4998,GWAS_ID_4999,GWAS_ID_5000,GWAS_ID_5001,GWAS_ID_5002 RMVar_hsa_circ_264822 43583 RMVar_ID_43583 Human_SNP_ID_40630625 A-to-I Human chr1 - 179587114 179587114 179587114 GGGTTCCCACCAGAACCAGAGGAATCTCGCTCATGTTCCGATAGTTGGCCATTCCACTGTAGTAA GGGTTCCCACCAGAACCAGAGGAATCTCGCTCGTGTTCCGATAGTTGGCCATTCCACTGTAGTAA T C lnc-NPHS2-2 RNACentral:URS00008B8FA7 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1001933047 Functional Loss SNV dbSNP153 33..33 33 - - - 43584 RMVar_ID_43584 Human_SNP_ID_40684114 A-to-I Human chr1 - 179818163 179818163 179818163 TCAGGCACTGATGGAGGCATTTTCCAAAGAACAGTGACAAGGACGGCCAGCACCTCTCTTGCATT TCAGGCACTGATGGAGGCATTTTCCAAAGAACGGTGACAAGGACGGCCAGCACCTCTCTTGCATT T C AL359853.1 Ensembl:ENSG00000229407 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1378453446 Functional Loss SNV dbSNP153 33..33 33 - - - 43585 RMVar_ID_43585 Human_SNP_ID_40684295 A-to-I Human chr1 - 179818798 179818798 179818798 CTTGTCACTGTTCTTTAGAAAATGCCTCCGTCAGTGCCTGAGGTTCAAGGAGTGTAGGCCGTTTT CTTGTCACTGTTCTTTAGAAAATGCCTCCGTCCGTGCCTGAGGTTCAAGGAGTGTAGGCCGTTTT T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1363618485 Functional Loss SNV dbSNP153 33..33 33 - - - 43586 RMVar_ID_43586 Human_SNP_ID_40691636 A-to-I Human chr1 - 179849301 179849301 179849301 TTGAAGCTGTGGTGAGCCGAAATTTCAGCACTACACTCCAGCCTTGTTGACAGAGTGAGACCCTG TTGAAGCTGTGGTGAGCCGAAATTTCAGCACTGCACTCCAGCCTTGTTGACAGAGTGAGACCCTG T C TOR1AIP2 Ensembl:ENSG00000169905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1329378649 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_138015,RMVar_hsa_circ_138016,RMVar_hsa_circ_60649 43587 RMVar_ID_43587 Human_SNP_ID_40691708 A-to-I Human chr1 - 179849712 179849712 179849712 TTACTTACACCTCTAGTCCCAGTTACTTGGGAAGCTGAGTTGGGAGGATTGCTTGAGCCCAGGAG TTACTTACACCTCTAGTCCCAGTTACTTGGGAGGCTGAGTTGGGAGGATTGCTTGAGCCCAGGAG T C TOR1AIP2 Ensembl:ENSG00000169905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1026485512 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_138015,RMVar_hsa_circ_138016,RMVar_hsa_circ_60649 43588 RMVar_ID_43588 Human_SNP_ID_40691709 A-to-I Human chr1 - 179849712 179849712 179849712 TTACTTACACCTCTAGTCCCAGTTACTTGGGAAGCTGAGTTGGGAGGATTGCTTGAGCCCAGGAG TTACTTACACCTCTAGTCCCAGTTACTTGGGACGCTGAGTTGGGAGGATTGCTTGAGCCCAGGAG T G TOR1AIP2 Ensembl:ENSG00000169905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1026485512 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_138015,RMVar_hsa_circ_138016,RMVar_hsa_circ_60649 43589 RMVar_ID_43589 Human_SNP_ID_40693279 A-to-I Human chr1 - 179856640 179856640 179856640 TTCACTCCAGCCTATGCGAAGAGTGAGATTCTATCTTGGGGGGGAAAAAAAGATTGACCTGCCTC TTCACTCCAGCCTATGCGAAGAGTGAGATTCTGTCTTGGGGGGGAAAAAAAGATTGACCTGCCTC T C TOR1AIP2 Ensembl:ENSG00000169905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1261786560 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_138016,RMVar_hsa_circ_60649,RMVar_hsa_circ_311431,RMVar_hsa_circ_334184 43590 RMVar_ID_43590 Human_SNP_ID_40693302 A-to-I Human chr1 - 179856713 179856713 179856713 GCTATGAAGGCTGAGGCACGAGAATCGCTTGAACCTGGAAGTTGGAGGTTGCGGTGAGCCAAGAT GCTATGAAGGCTGAGGCACGAGAATCGCTTGAGCCTGGAAGTTGGAGGTTGCGGTGAGCCAAGAT T C TOR1AIP2 Ensembl:ENSG00000169905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1317050754 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_138016,RMVar_hsa_circ_60649,RMVar_hsa_circ_311431,RMVar_hsa_circ_334184 43591 RMVar_ID_43591 Human_SNP_ID_40693975 A-to-I Human chr1 - 179859888 179859888 179859888 ATGAGCTTGAGGCTGCAGTGAGCTATGATGGTACTACTGCCCTCCAGCCTGGGCAACAGAGTAAG ATGAGCTTGAGGCTGCAGTGAGCTATGATGGTGCTACTGCCCTCCAGCCTGGGCAACAGAGTAAG T C TOR1AIP2 Ensembl:ENSG00000169905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs533702324 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_138016,RMVar_hsa_circ_60649,RMVar_hsa_circ_311431,RMVar_hsa_circ_334184 43592 RMVar_ID_43592 Human_SNP_ID_40693991 A-to-I Human chr1 - 179859961 179859961 179859961 GTGGTGGTATGTGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGTGGGAGGATCACTTGAGCCTC GTGGTGGTATGTGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGTGGGAGGATCACTTGAGCCTC T C TOR1AIP2 Ensembl:ENSG00000169905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1191212143 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_138016,RMVar_hsa_circ_60649,RMVar_hsa_circ_311431,RMVar_hsa_circ_334184 43593 RMVar_ID_43593 Human_SNP_ID_40694013 A-to-I Human chr1 - 179860075 179860075 179860075 GGGAGGCTGAGGCAGGAGGATGGCTTGAGCCCAGGAGTTCAAAACAAGCCTGAGCAACATAGTGA GGGAGGCTGAGGCAGGAGGATGGCTTGAGCCCGGGAGTTCAAAACAAGCCTGAGCAACATAGTGA T C TOR1AIP2 Ensembl:ENSG00000169905 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1171148517 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_138016,RMVar_hsa_circ_60649,RMVar_hsa_circ_311431,RMVar_hsa_circ_334184 43594 RMVar_ID_43594 Human_SNP_ID_40694101 A-to-I Human chr1 - 179860432 179860432 179860432 TGTCACCTAGGCTGGAGTGCAGTGGCGCCATCATGGCTCACTGCAGCCTTGACCTTCTGGGCTCA TGTCACCTAGGCTGGAGTGCAGTGGCGCCATCGTGGCTCACTGCAGCCTTGACCTTCTGGGCTCA T C TOR1AIP2 Ensembl:ENSG00000169905 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs779407563 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_138016,RMVar_hsa_circ_60649,RMVar_hsa_circ_311431,RMVar_hsa_circ_334184 43595 RMVar_ID_43595 Human_SNP_ID_40694608 A-to-I Human chr1 - 179862852 179862852 179862852 ACGATCTCGGCTTACTGTAACCTCCACCTCCTAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTG ACGATCTCGGCTTACTGTAACCTCCACCTCCTGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTG T C TOR1AIP2 Ensembl:ENSG00000169905 Protein coding intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1398688963 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10677330,Human_RBP_ID_18220640 RMVar_hsa_circ_138016,RMVar_hsa_circ_60649,RMVar_hsa_circ_311431,RMVar_hsa_circ_334184 43596 RMVar_ID_43596 Human_SNP_ID_40696412 A-to-I Human chr1 - 179870207 179870207 179870207 TTTTTAGTAGAGACAGGGTTTCACCATGTGTTAGCCAGGATGGTCTCCATCTCCTGACCTCGTGA TTTTTAGTAGAGACAGGGTTTCACCATGTGTTGGCCAGGATGGTCTCCATCTCCTGACCTCGTGA T C TOR1AIP2 Ensembl:ENSG00000169905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs541444879 Functional Loss SNV dbSNP153 33..33 33 - - - 43597 RMVar_ID_43597 Human_SNP_ID_40696425 A-to-I Human chr1 - 179870234 179870234 179870234 CCACCACGGCTGGCTAATTTTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTGTTAGCCAG CCACCACGGCTGGCTAATTTTTTTGTATTTTTCGTAGAGACAGGGTTTCACCATGTGTTAGCCAG T G TOR1AIP2 Ensembl:ENSG00000169905 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982721257 Functional Loss SNV dbSNP153 33..33 33 - - - 43598 RMVar_ID_43598 Human_SNP_ID_40708761 A-to-I Human chr1 + 179919248 179919248 179919248 ACCATGCTTATTGCCCTCCAGTCTGGGCAACAAAAATGAAACTCCGTCTCAAAAAAAAAAAAGTA ACCATGCTTATTGCCCTCCAGTCTGGGCAACAGAAATGAAACTCCGTCTCAAAAAAAAAAAAGTA A G TOR1AIP1 Ensembl:ENSG00000143337 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1220195855 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5722372,Human_RBP_ID_8170938 RMVar_hsa_circ_86132,RMVar_hsa_circ_138020 43599 RMVar_ID_43599 Human_SNP_ID_127850340 A-to-I Human chr3 + 30627577 30627577 30627577 TCTATTATGAAATTGGGAAAAATTATGTAATTATCTCTCTAAGATGGTCTTAGATCCACTGTTCA TCTATTATGAAATTGGGAAAAATTATGTAATTCTCTCTCTAAGATGGTCTTAGATCCACTGTTCA A C TGFBR2 Ensembl:ENSG00000163513 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs923982728 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105592,RMVar_hsa_circ_309171,RMVar_hsa_circ_216605,RMVar_hsa_circ_309871 43600 RMVar_ID_43600 Human_SNP_ID_127850353 A-to-I Human chr3 + 30627612 30627612 30627612 TCTCTAAGATGGTCTTAGATCCACTGTTCAATAGAACTTTCTGCAGAGATGAAAATATCTTATAC TCTCTAAGATGGTCTTAGATCCACTGTTCAATGGAACTTTCTGCAGAGATGAAAATATCTTATAC A G TGFBR2 Ensembl:ENSG00000163513 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1377049256 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17573536 RMVar_hsa_circ_105592,RMVar_hsa_circ_309171,RMVar_hsa_circ_216605,RMVar_hsa_circ_309871 43601 RMVar_ID_43601 Human_SNP_ID_127866581 A-to-I Human chr3 + 30693667 30693667 30693667 ATAGAGGCGCCTAGAAATTCCACTTGCACCGTAGGGCATGCTGATACCATCCCAATAGCTGTTGC ATAGAGGCGCCTAGAAATTCCACTTGCACCGTGGGGCATGCTGATACCATCCCAATAGCTGTTGC A G TGFBR2 Ensembl:ENSG00000163513 Protein coding 3'UTR GSE100210;GSE99789 HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 29129909,29796672 RNA-Seq:(High) rs916225952 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14786035 43602 RMVar_ID_43602 Human_SNP_ID_128101949 A-to-I Human chr3 + 31608839 31608839 31608839 GTAGTCGACAATAAGAAAAGGATGTGTTGGCCAGGTGCAGTGGCTCACGCCTGTAATCCCAGCAC GTAGTCGACAATAAGAAAAGGATGTGTTGGCCGGGTGCAGTGGCTCACGCCTGTAATCCCAGCAC A G STT3B Ensembl:ENSG00000163527 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1057276414 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1440,RMVar_hsa_circ_100060,RMVar_hsa_circ_111589,RMVar_hsa_circ_370304,RMVar_hsa_circ_120758,RMVar_hsa_circ_102289,RMVar_hsa_circ_216617,RMVar_hsa_circ_71824,RMVar_hsa_circ_216619,RMVar_hsa_circ_216620,RMVar_hsa_circ_216618,RMVar_hsa_circ_90396,RMVar_hsa_circ_216616,RMVar_hsa_circ_216627 43603 RMVar_ID_43603 Human_SNP_ID_128112539 A-to-I Human chr3 - 31650395 31650395 31650395 ACCACCATGCCCGGCTAATTTATTGCATTTTTAGTAGAGACGGGGTTTCACCATGTTAGCCAGGA ACCACCATGCCCGGCTAATTTATTGCATTTTTGGTAGAGACGGGGTTTCACCATGTTAGCCAGGA T C lnc-OSBPL10-6 RNACentral:URS0000D5C892 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1245992437 Functional Loss SNV dbSNP153 33..33 33 - - - 43604 RMVar_ID_43604 Human_SNP_ID_128169475 A-to-I Human chr3 - 31864939 31864939 31864939 ACATAGGCCTTACTGATCTGAAGGCAGGAGCTAATGTTCTCTGTGGTCCGGGTCAGCTACTTGTT ACATAGGCCTTACTGATCTGAAGGCAGGAGCTGATGTTCTCTGTGGTCCGGGTCAGCTACTTGTT T C OSBPL10 Ensembl:ENSG00000144645 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs371640490 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40000,RMVar_hsa_circ_328552,RMVar_hsa_circ_216640,RMVar_hsa_circ_320732,RMVar_hsa_circ_278244,RMVar_hsa_circ_216642 43605 RMVar_ID_43605 Human_SNP_ID_128193516 A-to-I Human chr3 - 31957023 31957023 31957023 TCAGGTGATCCTCCCACTTCAGTTTCCTGAATAGCTGGGACCACAGGTGTGTACCACCACATCCA TCAGGTGATCCTCCCACTTCAGTTTCCTGAATGGCTGGGACCACAGGTGTGTACCACCACATCCA T C OSBPL10 Ensembl:ENSG00000144645 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1304190112 Functional Loss SNV dbSNP153 33..33 33 - - - 43606 RMVar_ID_43606 Human_SNP_ID_128197343 A-to-I Human chr3 - 31969549 31969549 31969549 ATCCACCCACCTCAGCCTCCCAAAGTAGTGCTAGGATTACAGGCGTGAGCCACCGTGCCCAGCGA ATCCACCCACCTCAGCCTCCCAAAGTAGTGCTGGGATTACAGGCGTGAGCCACCGTGCCCAGCGA T C OSBPL10 Ensembl:ENSG00000144645 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1449827195 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23312566 43607 RMVar_ID_43607 Human_SNP_ID_128197350 A-to-I Human chr3 - 31969568 31969568 31969568 GAACACCTGACCTCAACTAATCCACCCACCTCAGCCTCCCAAAGTAGTGCTAGGATTACAGGCGT GAACACCTGACCTCAACTAATCCACCCACCTCGGCCTCCCAAAGTAGTGCTAGGATTACAGGCGT T C OSBPL10 Ensembl:ENSG00000144645 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1272121205 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23312566 43608 RMVar_ID_43608 Human_SNP_ID_128240340 A-to-I Human chr3 + 32150597 32150597 32150597 CAACCTCTGCCTTCCAGGTTCAAGGAATTCTCATGCCTCAGCCTCCCAAGTAGCTGGGATTACAG CAACCTCTGCCTTCCAGGTTCAAGGAATTCTCGTGCCTCAGCCTCCCAAGTAGCTGGGATTACAG A G GPD1L Ensembl:ENSG00000152642 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1469977447 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81652,RMVar_hsa_circ_339852,RMVar_hsa_circ_216648 43609 RMVar_ID_43609 Human_SNP_ID_128240595 A-to-I Human chr3 + 32151694 32151693 32151694 GGAGACAGAGTTTCACCATGTTGCCCAGTCTGATCTCAAACTCCTGGACTCAAGTGATCCATCAG GGAGACAGAGTTTCACCATGTTGCCCAGTCTG_TCTCAAACTCCTGGACTCAAGTGATCCATCAG GA G GPD1L Ensembl:ENSG00000152642 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1423391627 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_14789180 RMVar_hsa_circ_81652,RMVar_hsa_circ_339852,RMVar_hsa_circ_216648 43610 RMVar_ID_43610 Human_SNP_ID_128376184 A-to-I Human chr3 + 32693641 32693641 32693641 ACTGCTCACTGCATCCTTGACTTCCCAGGCTCAAGCGATCCTCCCACCTCAGCCTCCCAAGTAGC ACTGCTCACTGCATCCTTGACTTCCCAGGCTCGAGCGATCCTCCCACCTCAGCCTCCCAAGTAGC A G CNOT10 Ensembl:ENSG00000182973 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417449445 Functional Loss SNV dbSNP153 33..33 33 - - - 43611 RMVar_ID_43611 Human_SNP_ID_128384640 A-to-I Human chr3 + 32726145 32726145 32726145 TTTTGTGTTTTTTGTAAAGATAGGGTTTCACCATGTTGCCCAGGCTGGTCTGGAACTCCTGGCTT TTTTGTGTTTTTTGTAAAGATAGGGTTTCACCTTGTTGCCCAGGCTGGTCTGGAACTCCTGGCTT A T CNOT10 Ensembl:ENSG00000182973 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1230965237 Functional Loss SNV dbSNP153 33..33 33 - - - 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_43035,RMVar_hsa_circ_377129,RMVar_hsa_circ_39744 43612 RMVar_ID_43612 Human_SNP_ID_128384964 A-to-I Human chr3 + 32727194 32727194 32727194 GAAACTTTATATAGACTCTAAAAATGTTGGCTAGGAAAGATGGCTCATGCCTGTAATCCCAACAT GAAACTTTATATAGACTCTAAAAATGTTGGCTGGGAAAGATGGCTCATGCCTGTAATCCCAACAT A G CNOT10 Ensembl:ENSG00000182973 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1192156847 Functional Loss SNV dbSNP153 33..33 33 - - - 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_43035,RMVar_hsa_circ_377129,RMVar_hsa_circ_39744 43613 RMVar_ID_43613 Human_SNP_ID_128386487 A-to-I Human chr3 + 32732641 32732641 32732641 AAAAAAAAAGGTAGATACAGGGGGGTCTCACTATGTTGCCCAGGCTGGTCTCACACTCCTGGTTT AAAAAAAAAGGTAGATACAGGGGGGTCTCACTGTGTTGCCCAGGCTGGTCTCACACTCCTGGTTT A G CNOT10 Ensembl:ENSG00000182973 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs900978405 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_304329,RMVar_hsa_circ_341281,RMVar_hsa_circ_358775,RMVar_hsa_circ_326007,RMVar_hsa_circ_14283,RMVar_hsa_circ_216684,RMVar_hsa_circ_216685,RMVar_hsa_circ_304200,RMVar_hsa_circ_309712,RMVar_hsa_circ_8817,RMVar_hsa_circ_216689,RMVar_hsa_circ_216690,RMVar_hsa_circ_216688,RMVar_hsa_circ_46950,RMVar_hsa_circ_354902,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 43614 RMVar_ID_43614 Human_SNP_ID_128388132 A-to-I Human chr3 + 32739004 32739004 32739004 TCGGCTCACTGCAACCTCTGCCTACCAGTTTCAGGCGATTCTCCTGCCTCAGCTTCCTAAGAAGC TCGGCTCACTGCAACCTCTGCCTACCAGTTTCGGGCGATTCTCCTGCCTCAGCTTCCTAAGAAGC A G CNOT10 Ensembl:ENSG00000182973 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1280751898 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2780998,Human_RBP_ID_8570979,Human_RBP_ID_14792620 RMVar_hsa_circ_18534,RMVar_hsa_circ_341281,RMVar_hsa_circ_358775,RMVar_hsa_circ_216688,RMVar_hsa_circ_39744,RMVar_hsa_circ_115333,RMVar_hsa_circ_17400,RMVar_hsa_circ_216699,RMVar_hsa_circ_342342,RMVar_hsa_circ_371150,RMVar_hsa_circ_216703,RMVar_hsa_circ_216704 43615 RMVar_ID_43615 Human_SNP_ID_128391112 A-to-I Human chr3 + 32750077 32750077 32750077 TGTCTCTACAAAAAATTTAGTCTGGTCATGATAGCGCGTGCCTGTATTCCTAGCTACTTGGGAGA TGTCTCTACAAAAAATTTAGTCTGGTCATGATGGCGCGTGCCTGTATTCCTAGCTACTTGGGAGA A G CNOT10 Ensembl:ENSG00000182973 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1418362073 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14792863 RMVar_hsa_circ_18534,RMVar_hsa_circ_341281,RMVar_hsa_circ_358775,RMVar_hsa_circ_216688,RMVar_hsa_circ_39744,RMVar_hsa_circ_115333,RMVar_hsa_circ_17400,RMVar_hsa_circ_216699,RMVar_hsa_circ_342342,RMVar_hsa_circ_371150,RMVar_hsa_circ_216703,RMVar_hsa_circ_216704 43616 RMVar_ID_43616 Human_SNP_ID_128391857 A-to-I Human chr3 + 32752999 32752999 32752999 GATACTCTAATCGACGAGGACCCCCAGGCGGCATTAGAGGAGCTGACTAAGGCTTTGGAACAGAA GATACTCTAATCGACGAGGACCCCCAGGCGGCGTTAGAGGAGCTGACTAAGGCTTTGGAACAGAA A G SUGT1P2,CNOT10 Ensembl:ENSG00000213842,Ensembl:ENSG00000182973 Pseudogene,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1244074613 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_936416,Human_RBP_ID_1961305,Human_RBP_ID_7187793,Human_RBP_ID_8875815,Human_RBP_ID_14995357,Human_RBP_ID_17405132,Human_RBP_ID_20971635,Human_RBP_ID_22526825 RMVar_hsa_circ_18534,RMVar_hsa_circ_341281,RMVar_hsa_circ_358775,RMVar_hsa_circ_216688,RMVar_hsa_circ_39744,RMVar_hsa_circ_115333,RMVar_hsa_circ_17400,RMVar_hsa_circ_216699,RMVar_hsa_circ_342342,RMVar_hsa_circ_371150,RMVar_hsa_circ_216703,RMVar_hsa_circ_216704 43617 RMVar_ID_43617 Human_SNP_ID_128397182 A-to-I Human chr3 + 32772959 32772959 32772959 GTGATCTTGGCTCACTGCAGCCTTGACCTCCCAGGTTCAAGCAGCCCTCCTGCCTCAGCCCCCCA GTGATCTTGGCTCACTGCAGCCTTGACCTCCCGGGTTCAAGCAGCCCTCCTGCCTCAGCCCCCCA A G CNOT10 Ensembl:ENSG00000182973 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs546200666 Functional Loss SNV dbSNP153 33..33 33 - - - 43618 RMVar_ID_43618 Human_SNP_ID_128397202 A-to-I Human chr3 + 32772991 32772991 32772991 AGGTTCAAGCAGCCCTCCTGCCTCAGCCCCCCAAGTAGCTGGGACTACAGGCATGCACCACCATG AGGTTCAAGCAGCCCTCCTGCCTCAGCCCCCCGAGTAGCTGGGACTACAGGCATGCACCACCATG A G CNOT10 Ensembl:ENSG00000182973 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1192828734 Functional Loss SNV dbSNP153 33..33 33 - - - 43619 RMVar_ID_43619 Human_SNP_ID_128469632 A-to-I Human chr3 - 33035214 33035214 33035214 TTGCCCGGGCTGCTCTCGAACTCCTGACCTCAAGCAATCCTCCCACCTTGGCCTCCCAGAGTGCT TTGCCCGGGCTGCTCTCGAACTCCTGACCTCACGCAATCCTCCCACCTTGGCCTCCCAGAGTGCT T G GLB1 Ensembl:ENSG00000170266 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1231614303 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5895,RMVar_hsa_circ_37176,RMVar_hsa_circ_344468,RMVar_hsa_circ_120518,RMVar_hsa_circ_280507,RMVar_hsa_circ_71996,RMVar_hsa_circ_124077,RMVar_hsa_circ_216710,RMVar_hsa_circ_216709,RMVar_hsa_circ_42932,RMVar_hsa_circ_216714,RMVar_hsa_circ_42418,RMVar_hsa_circ_216715,RMVar_hsa_circ_343821,RMVar_hsa_circ_378619,RMVar_hsa_circ_108159 43620 RMVar_ID_43620 Human_SNP_ID_128470078 A-to-I Human chr3 - 33037174 33037174 33037174 TGGCATGGTGGCGCACACCTGTAATTCCAGCTACTCGGGAGACTGGGGCAGGAGAATCGCTTGAA TGGCATGGTGGCGCACACCTGTAATTCCAGCTGCTCGGGAGACTGGGGCAGGAGAATCGCTTGAA T C GLB1 Ensembl:ENSG00000170266 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1415642225 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5895,RMVar_hsa_circ_37176,RMVar_hsa_circ_344468,RMVar_hsa_circ_120518,RMVar_hsa_circ_280507,RMVar_hsa_circ_71996,RMVar_hsa_circ_124077,RMVar_hsa_circ_216710,RMVar_hsa_circ_216709,RMVar_hsa_circ_42932,RMVar_hsa_circ_216714,RMVar_hsa_circ_42418,RMVar_hsa_circ_216715,RMVar_hsa_circ_343821,RMVar_hsa_circ_378619,RMVar_hsa_circ_108159 43621 RMVar_ID_43621 Human_SNP_ID_128476293 A-to-I Human chr3 - 33062705 33062705 33062705 CGGCTCACTGCAACCTCCACCTCCTGGGTTCAAGTGATCCTCCTGCCTCAGCCTCCTGAATAGCT CGGCTCACTGCAACCTCCACCTCCTGGGTTCAGGTGATCCTCCTGCCTCAGCCTCCTGAATAGCT T C GLB1 Ensembl:ENSG00000170266 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1163867701 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28482,RMVar_hsa_circ_5895,RMVar_hsa_circ_37176,RMVar_hsa_circ_344468,RMVar_hsa_circ_120518,RMVar_hsa_circ_124077,RMVar_hsa_circ_216709,RMVar_hsa_circ_216714,RMVar_hsa_circ_331895,RMVar_hsa_circ_216715,RMVar_hsa_circ_378619,RMVar_hsa_circ_108159,RMVar_hsa_circ_333911,RMVar_hsa_circ_314096,RMVar_hsa_circ_216717,RMVar_hsa_circ_216716,RMVar_hsa_circ_293853,RMVar_hsa_circ_216722,RMVar_hsa_circ_216723,RMVar_hsa_circ_107103,RMVar_hsa_circ_216724,RMVar_hsa_circ_371210 43622 RMVar_ID_43622 Human_SNP_ID_128476299 A-to-I Human chr3 - 33062725 33062725 33062725 TGAGTGCAGTGATGAGATCTCGGCTCACTGCAACCTCCACCTCCTGGGTTCAAGTGATCCTCCTG TGAGTGCAGTGATGAGATCTCGGCTCACTGCAGCCTCCACCTCCTGGGTTCAAGTGATCCTCCTG T C GLB1 Ensembl:ENSG00000170266 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913504642 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28482,RMVar_hsa_circ_5895,RMVar_hsa_circ_37176,RMVar_hsa_circ_344468,RMVar_hsa_circ_120518,RMVar_hsa_circ_124077,RMVar_hsa_circ_216709,RMVar_hsa_circ_216714,RMVar_hsa_circ_331895,RMVar_hsa_circ_216715,RMVar_hsa_circ_378619,RMVar_hsa_circ_108159,RMVar_hsa_circ_333911,RMVar_hsa_circ_314096,RMVar_hsa_circ_216717,RMVar_hsa_circ_216716,RMVar_hsa_circ_293853,RMVar_hsa_circ_216722,RMVar_hsa_circ_216723,RMVar_hsa_circ_107103,RMVar_hsa_circ_216724,RMVar_hsa_circ_371210 43623 RMVar_ID_43623 Human_SNP_ID_128492399 A-to-I Human chr3 + 33124555 33124555 33124555 CCTGCGAGGGTTCCAGGGAGATCAAGGACTTCAAGGATTTCTACCTTTCCATAGCAGGTTGGTGG CCTGCGAGGGTTCCAGGGAGATCAAGGACTTCCAGGATTTCTACCTTTCCATAGCAGGTTGGTGG A C CRTAP Ensembl:ENSG00000170275 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs779832379 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_600343,Human_RBP_ID_1961349,Human_RBP_ID_5120221,Human_RBP_ID_8571046,Human_RBP_ID_9139532,Human_RBP_ID_9393396,Human_RBP_ID_14794253,Human_RBP_ID_17404525,Human_RBP_ID_18194510,Human_RBP_ID_18338034,Human_RBP_ID_18446495,Human_RBP_ID_22769154 Human_Splice_Rec_406169,Human_Splice_Rec_406179,Human_Splice_Rec_406189 RMVar_hsa_circ_120787,RMVar_hsa_circ_345660,RMVar_hsa_circ_216730,RMVar_hsa_circ_342857,RMVar_hsa_circ_272279,RMVar_hsa_circ_366801,RMVar_hsa_circ_314193 43624 RMVar_ID_43624 Human_SNP_ID_128496788 A-to-I Human chr3 + 33142794 33142794 33142794 CTGCTGCATCAGCCTCCCGAGTACCTGGGATTACAGGCATGTGCCACCACGCCCGGCTAATTTTG CTGCTGCATCAGCCTCCCGAGTACCTGGGATTGCAGGCATGTGCCACCACGCCCGGCTAATTTTG A G CRTAP Ensembl:ENSG00000170275 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs11558341 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1400135 RMVar_hsa_circ_88820,RMVar_hsa_circ_216733 43625 RMVar_ID_43625 Human_SNP_ID_128499161 A-to-I Human chr3 - 33152167 33152167 33152167 GTGATCTGCCCTCCTTAGCCTCCCAAAGTGCTAGGATTCCAGGTGTGAGCCACATCACAGTATTA GTGATCTGCCCTCCTTAGCCTCCCAAAGTGCTGGGATTCCAGGTGTGAGCCACATCACAGTATTA T C SUSD5 Ensembl:ENSG00000173705 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355939643 Functional Loss SNV dbSNP153 33..33 33 - - - 43626 RMVar_ID_43626 Human_SNP_ID_128499921 A-to-I Human chr3 + 33154450 33154450 33154450 GAGGATGAGACATGAGAATCGCTTGAACCCGGAAGGCGGACGTTGCAGTGAGCCAACATCGTACC GAGGATGAGACATGAGAATCGCTTGAACCCGGCAGGCGGACGTTGCAGTGAGCCAACATCGTACC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1480978180 Functional Loss SNV dbSNP153 33..33 33 - - - 43627 RMVar_ID_43627 Human_SNP_ID_128538405 A-to-I Human chr3 + 33313648 33313648 33313648 TTTTATTTTTTTTGTAGTGGCAGGGTCTTATTATGTTGCCCAGGCTGGTCTCAAACTCCTGGCCT TTTTATTTTTTTTGTAGTGGCAGGGTCTTATTGTGTTGCCCAGGCTGGTCTCAAACTCCTGGCCT A G FBXL2 Ensembl:ENSG00000153558 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1418911213 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33608,RMVar_hsa_circ_95150,RMVar_hsa_circ_26392,RMVar_hsa_circ_216734,RMVar_hsa_circ_41574,RMVar_hsa_circ_30476 43628 RMVar_ID_43628 Human_SNP_ID_128538406 A-to-I Human chr3 + 33313648 33313648 33313648 TTTTATTTTTTTTGTAGTGGCAGGGTCTTATTATGTTGCCCAGGCTGGTCTCAAACTCCTGGCCT TTTTATTTTTTTTGTAGTGGCAGGGTCTTATTTTGTTGCCCAGGCTGGTCTCAAACTCCTGGCCT A T FBXL2 Ensembl:ENSG00000153558 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1418911213 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33608,RMVar_hsa_circ_95150,RMVar_hsa_circ_26392,RMVar_hsa_circ_216734,RMVar_hsa_circ_41574,RMVar_hsa_circ_30476 43629 RMVar_ID_43629 Human_SNP_ID_128556287 A-to-I Human chr3 - 33388411 33388411 33388411 TGAAACAGGCTAAATAAATTTTGGCACCAGCAAATTTGTTACTTTGTTTTTTTAATAGTAGGATG TGAAACAGGCTAAATAAATTTTGGCACCAGCAGATTTGTTACTTTGTTTTTTTAATAGTAGGATG T C UBP1 Ensembl:ENSG00000153560 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs537951399 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2781443,Human_RBP_ID_3705526,Human_RBP_ID_7188471,Human_RBP_ID_8571106,Human_RBP_ID_17660815,Human_RBP_ID_26771199,Human_RBP_ID_27717998 Human_miRNA_ID_1763020,Human_miRNA_ID_3083631 RMVar_hsa_circ_104269,RMVar_hsa_circ_216744 43630 RMVar_ID_43630 Human_SNP_ID_128556288 A-to-I Human chr3 - 33388411 33388411 33388411 TGAAACAGGCTAAATAAATTTTGGCACCAGCAAATTTGTTACTTTGTTTTTTTAATAGTAGGATG TGAAACAGGCTAAATAAATTTTGGCACCAGCACATTTGTTACTTTGTTTTTTTAATAGTAGGATG T G UBP1 Ensembl:ENSG00000153560 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs537951399 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2781443,Human_RBP_ID_3705526,Human_RBP_ID_7188471,Human_RBP_ID_8571106,Human_RBP_ID_17660815,Human_RBP_ID_26771199,Human_RBP_ID_27717998 Human_miRNA_ID_1763020,Human_miRNA_ID_3083631 RMVar_hsa_circ_104269,RMVar_hsa_circ_216744 43631 RMVar_ID_43631 Human_SNP_ID_128563864 A-to-I Human chr3 - 33418371 33418371 33418371 GGGCACCTGTAATCCCAGGTACTCAGGAGTCCAAGGCAGGGAGAATTGCTTGAACCTGGGAGGTG GGGCACCTGTAATCCCAGGTACTCAGGAGTCCGAGGCAGGGAGAATTGCTTGAACCTGGGAGGTG T C UBP1 Ensembl:ENSG00000153560 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs941184586 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_216745,RMVar_hsa_circ_322013,RMVar_hsa_circ_216746,RMVar_hsa_circ_319653,RMVar_hsa_circ_285711,RMVar_hsa_circ_216748,RMVar_hsa_circ_290809,RMVar_hsa_circ_116873,RMVar_hsa_circ_216751,RMVar_hsa_circ_271074,RMVar_hsa_circ_216759,RMVar_hsa_circ_216752,RMVar_hsa_circ_216753,RMVar_hsa_circ_126430,RMVar_hsa_circ_289292,RMVar_hsa_circ_216756,RMVar_hsa_circ_216757,RMVar_hsa_circ_216758,RMVar_hsa_circ_375395,RMVar_hsa_circ_315165,RMVar_hsa_circ_216762,RMVar_hsa_circ_216760,RMVar_hsa_circ_272284,RMVar_hsa_circ_59590,RMVar_hsa_circ_287651,RMVar_hsa_circ_216761,RMVar_hsa_circ_292801,RMVar_hsa_circ_305005 43632 RMVar_ID_43632 Human_SNP_ID_128564182 A-to-I Human chr3 - 33419516 33419516 33419516 TCAAGTGATTCTCCTGCCTCAGCCTCTGGAGTAGCTGGCATTACAGGTGCCTGCCACCACGCCCA TCAAGTGATTCTCCTGCCTCAGCCTCTGGAGTGGCTGGCATTACAGGTGCCTGCCACCACGCCCA T C UBP1 Ensembl:ENSG00000153560 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs897941108 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_216745,RMVar_hsa_circ_322013,RMVar_hsa_circ_216746,RMVar_hsa_circ_319653,RMVar_hsa_circ_285711,RMVar_hsa_circ_216748,RMVar_hsa_circ_290809,RMVar_hsa_circ_116873,RMVar_hsa_circ_216751,RMVar_hsa_circ_271074,RMVar_hsa_circ_216759,RMVar_hsa_circ_216752,RMVar_hsa_circ_216753,RMVar_hsa_circ_126430,RMVar_hsa_circ_289292,RMVar_hsa_circ_216756,RMVar_hsa_circ_216757,RMVar_hsa_circ_216758,RMVar_hsa_circ_375395,RMVar_hsa_circ_315165,RMVar_hsa_circ_216762,RMVar_hsa_circ_216760,RMVar_hsa_circ_272284,RMVar_hsa_circ_59590,RMVar_hsa_circ_287651,RMVar_hsa_circ_216761,RMVar_hsa_circ_292801,RMVar_hsa_circ_305005 43633 RMVar_ID_43633 Human_SNP_ID_128564405 A-to-I Human chr3 - 33420402 33420402 33420402 AGAATTGCTTGAATTTGGGAGAGGGAGGTTGCAGTGAGCCCAGATTGCACCACTGTACTCCAGCC AGAATTGCTTGAATTTGGGAGAGGGAGGTTGCGGTGAGCCCAGATTGCACCACTGTACTCCAGCC T C UBP1 Ensembl:ENSG00000153560 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1187300077 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_216745,RMVar_hsa_circ_322013,RMVar_hsa_circ_216746,RMVar_hsa_circ_319653,RMVar_hsa_circ_285711,RMVar_hsa_circ_216748,RMVar_hsa_circ_290809,RMVar_hsa_circ_116873,RMVar_hsa_circ_216751,RMVar_hsa_circ_271074,RMVar_hsa_circ_216759,RMVar_hsa_circ_216752,RMVar_hsa_circ_216753,RMVar_hsa_circ_126430,RMVar_hsa_circ_289292,RMVar_hsa_circ_216756,RMVar_hsa_circ_216757,RMVar_hsa_circ_216758,RMVar_hsa_circ_375395,RMVar_hsa_circ_315165,RMVar_hsa_circ_216762,RMVar_hsa_circ_216760,RMVar_hsa_circ_272284,RMVar_hsa_circ_59590,RMVar_hsa_circ_287651,RMVar_hsa_circ_216761,RMVar_hsa_circ_292801,RMVar_hsa_circ_305005 43634 RMVar_ID_43634 Human_SNP_ID_128564941 A-to-I Human chr3 - 33422625 33422625 33422625 GACCTCCCAGGCTAAAGTGATCCACCCACCCTAGCCTCCTGAGTAGCTGGGACTACAGGCACAGG GACCTCCCAGGCTAAAGTGATCCACCCACCCTCGCCTCCTGAGTAGCTGGGACTACAGGCACAGG T G UBP1 Ensembl:ENSG00000153560 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1004194169 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25732780 RMVar_hsa_circ_216745,RMVar_hsa_circ_322013,RMVar_hsa_circ_216746,RMVar_hsa_circ_319653,RMVar_hsa_circ_285711,RMVar_hsa_circ_216748,RMVar_hsa_circ_290809,RMVar_hsa_circ_116873,RMVar_hsa_circ_216751,RMVar_hsa_circ_271074,RMVar_hsa_circ_216759,RMVar_hsa_circ_216752,RMVar_hsa_circ_216753,RMVar_hsa_circ_126430,RMVar_hsa_circ_289292,RMVar_hsa_circ_216756,RMVar_hsa_circ_216757,RMVar_hsa_circ_216758,RMVar_hsa_circ_375395,RMVar_hsa_circ_315165,RMVar_hsa_circ_216762,RMVar_hsa_circ_216760,RMVar_hsa_circ_272284,RMVar_hsa_circ_59590,RMVar_hsa_circ_287651,RMVar_hsa_circ_216761,RMVar_hsa_circ_292801,RMVar_hsa_circ_305005 43635 RMVar_ID_43635 Human_SNP_ID_128565129 A-to-I Human chr3 - 33423219 33423219 33423219 CCTGGCCAACATGGTGAAACCCCGTCTCTACTAGAAATACAAAAATTAGCCAGGCATGGTGGCAC CCTGGCCAACATGGTGAAACCCCGTCTCTACTGGAAATACAAAAATTAGCCAGGCATGGTGGCAC T C UBP1 Ensembl:ENSG00000153560 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1472318449 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_216745,RMVar_hsa_circ_322013,RMVar_hsa_circ_216746,RMVar_hsa_circ_319653,RMVar_hsa_circ_285711,RMVar_hsa_circ_216748,RMVar_hsa_circ_290809,RMVar_hsa_circ_116873,RMVar_hsa_circ_216751,RMVar_hsa_circ_271074,RMVar_hsa_circ_216759,RMVar_hsa_circ_216752,RMVar_hsa_circ_216753,RMVar_hsa_circ_126430,RMVar_hsa_circ_289292,RMVar_hsa_circ_216756,RMVar_hsa_circ_216757,RMVar_hsa_circ_216758,RMVar_hsa_circ_375395,RMVar_hsa_circ_315165,RMVar_hsa_circ_216762,RMVar_hsa_circ_216760,RMVar_hsa_circ_272284,RMVar_hsa_circ_59590,RMVar_hsa_circ_287651,RMVar_hsa_circ_216761,RMVar_hsa_circ_292801,RMVar_hsa_circ_305005 43636 RMVar_ID_43636 Human_SNP_ID_128566334 A-to-I Human chr3 - 33427957 33427957 33427957 CGAACTCCTGACCTCAGGTGATCACCCACCTCAGCCTTCCAAAGTGCTGGAATTATAGGTGTGAG CGAACTCCTGACCTCAGGTGATCACCCACCTCGGCCTTCCAAAGTGCTGGAATTATAGGTGTGAG T C UBP1 Ensembl:ENSG00000153560 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs759229599 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116873,RMVar_hsa_circ_216752,RMVar_hsa_circ_126430,RMVar_hsa_circ_216757,RMVar_hsa_circ_105056,RMVar_hsa_circ_116582,RMVar_hsa_circ_216765,RMVar_hsa_circ_216767,RMVar_hsa_circ_98989,RMVar_hsa_circ_216766 43637 RMVar_ID_43637 Human_SNP_ID_128567401 A-to-I Human chr3 - 33432202 33432202 33432202 CTCCTACCTCTGCCTCCCTAGTAGCTGAGTTTATGAGTATGCGCCACCATGCCTGGCTAATTTTT CTCCTACCTCTGCCTCCCTAGTAGCTGAGTTTGTGAGTATGCGCCACCATGCCTGGCTAATTTTT T C UBP1 Ensembl:ENSG00000153560 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs111790600 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116873,RMVar_hsa_circ_216752,RMVar_hsa_circ_126430,RMVar_hsa_circ_216757,RMVar_hsa_circ_105056,RMVar_hsa_circ_116582,RMVar_hsa_circ_216765,RMVar_hsa_circ_216767,RMVar_hsa_circ_98989,RMVar_hsa_circ_216766 43638 RMVar_ID_43638 Human_SNP_ID_128567845 A-to-I Human chr3 - 33433853 33433853 33433853 GTGGCTATTTGCAGACTTGATCACTGCACACTACAGGCTCTAATTCCTGGGCTCAAGGGATTCTC GTGGCTATTTGCAGACTTGATCACTGCACACTGCAGGCTCTAATTCCTGGGCTCAAGGGATTCTC T C UBP1 Ensembl:ENSG00000153560 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1415676270 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116873,RMVar_hsa_circ_216752,RMVar_hsa_circ_126430,RMVar_hsa_circ_216757,RMVar_hsa_circ_105056,RMVar_hsa_circ_116582,RMVar_hsa_circ_216765,RMVar_hsa_circ_216767,RMVar_hsa_circ_98989,RMVar_hsa_circ_216766 43639 RMVar_ID_43639 Human_SNP_ID_128586146 A-to-I Human chr3 - 33505572 33505572 33505572 AATCACTTCATATATTATTGTAGCATGATTCTATTCATTTTGGCCAGCTCAGTGGTTGCTTAAGT AATCACTTCATATATTATTGTAGCATGATTCTGTTCATTTTGGCCAGCTCAGTGGTTGCTTAAGT T C CLASP2 Ensembl:ENSG00000163539 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1463432202 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14424,RMVar_hsa_circ_113585,RMVar_hsa_circ_304405,RMVar_hsa_circ_322875,RMVar_hsa_circ_336056,RMVar_hsa_circ_269578,RMVar_hsa_circ_21535,RMVar_hsa_circ_46762,RMVar_hsa_circ_18461,RMVar_hsa_circ_216771,RMVar_hsa_circ_216772,RMVar_hsa_circ_216770 43640 RMVar_ID_43640 Human_SNP_ID_128586163 A-to-I Human chr3 - 33505655 33505655 33505655 GGTTCAGATGTTATTAGTCTAATCCCTCCATTATATACCTTGCCCCATCATCTTTTCACCTAATG GGTTCAGATGTTATTAGTCTAATCCCTCCATTGTATACCTTGCCCCATCATCTTTTCACCTAATG T C CLASP2 Ensembl:ENSG00000163539 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1445944699 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14424,RMVar_hsa_circ_113585,RMVar_hsa_circ_304405,RMVar_hsa_circ_322875,RMVar_hsa_circ_336056,RMVar_hsa_circ_269578,RMVar_hsa_circ_21535,RMVar_hsa_circ_46762,RMVar_hsa_circ_18461,RMVar_hsa_circ_216771,RMVar_hsa_circ_216772,RMVar_hsa_circ_216770 43641 RMVar_ID_43641 Human_SNP_ID_128586168 A-to-I Human chr3 - 33505672 33505672 33505672 GTTAAGATTGATCAGTAGGTTCAGATGTTATTAGTCTAATCCCTCCATTATATACCTTGCCCCAT GTTAAGATTGATCAGTAGGTTCAGATGTTATTCGTCTAATCCCTCCATTATATACCTTGCCCCAT T G CLASP2 Ensembl:ENSG00000163539 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1485852078 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14424,RMVar_hsa_circ_113585,RMVar_hsa_circ_304405,RMVar_hsa_circ_322875,RMVar_hsa_circ_336056,RMVar_hsa_circ_269578,RMVar_hsa_circ_21535,RMVar_hsa_circ_46762,RMVar_hsa_circ_18461,RMVar_hsa_circ_216771,RMVar_hsa_circ_216772,RMVar_hsa_circ_216770 43642 RMVar_ID_43642 Human_SNP_ID_128586749 A-to-I Human chr3 - 33507791 33507790 33507792 TAACATCACTGAAGGTGGGACAACTAGACAAAAGTTTTCTTGCCTGGCTTGGTGGCTCACGCCTG TAACATCACTGAAGGTGGGACAACTAGACAA__GTTTTCTTGCCTGGCTTGGTGGCTCACGCCTG CTT C CLASP2 Ensembl:ENSG00000163539 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1378615595 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_25732901 RMVar_hsa_circ_14424,RMVar_hsa_circ_113585,RMVar_hsa_circ_304405,RMVar_hsa_circ_322875,RMVar_hsa_circ_336056,RMVar_hsa_circ_269578,RMVar_hsa_circ_21535,RMVar_hsa_circ_46762,RMVar_hsa_circ_18461,RMVar_hsa_circ_216771,RMVar_hsa_circ_216772,RMVar_hsa_circ_216770 43643 RMVar_ID_43643 Human_SNP_ID_128586756 A-to-I Human chr3 - 33507821 33507821 33507821 CTAACAACATCTGAACCTACTGACCAATCTTAACATCACTGAAGGTGGGACAACTAGACAAAAGT CTAACAACATCTGAACCTACTGACCAATCTTACCATCACTGAAGGTGGGACAACTAGACAAAAGT T G CLASP2 Ensembl:ENSG00000163539 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs919375049 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14424,RMVar_hsa_circ_113585,RMVar_hsa_circ_304405,RMVar_hsa_circ_322875,RMVar_hsa_circ_336056,RMVar_hsa_circ_269578,RMVar_hsa_circ_21535,RMVar_hsa_circ_46762,RMVar_hsa_circ_18461,RMVar_hsa_circ_216771,RMVar_hsa_circ_216772,RMVar_hsa_circ_216770 43644 RMVar_ID_43644 Human_SNP_ID_128593190 A-to-I Human chr3 - 33534327 33534327 33534327 GAACTCCTGGCCATAAGTGATCCTCCCACCTCAACCTCTCAAAGTGCTGGGATTGTAGGTGTGAG GAACTCCTGGCCATAAGTGATCCTCCCACCTCCACCTCTCAAAGTGCTGGGATTGTAGGTGTGAG T G CLASP2 Ensembl:ENSG00000163539 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985694855 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14424,RMVar_hsa_circ_113585,RMVar_hsa_circ_304405,RMVar_hsa_circ_269578,RMVar_hsa_circ_21535,RMVar_hsa_circ_46762,RMVar_hsa_circ_18461,RMVar_hsa_circ_2032,RMVar_hsa_circ_27031,RMVar_hsa_circ_61436,RMVar_hsa_circ_216772,RMVar_hsa_circ_286425,RMVar_hsa_circ_365293,RMVar_hsa_circ_265924,RMVar_hsa_circ_41418,RMVar_hsa_circ_42018,RMVar_hsa_circ_6897,RMVar_hsa_circ_277389,RMVar_hsa_circ_216774,RMVar_hsa_circ_326669,RMVar_hsa_circ_365318,RMVar_hsa_circ_286455,RMVar_hsa_circ_111230,RMVar_hsa_circ_120430,RMVar_hsa_circ_101772,RMVar_hsa_circ_216775,RMVar_hsa_circ_216777,RMVar_hsa_circ_216778,RMVar_hsa_circ_216779,RMVar_hsa_circ_216776,RMVar_hsa_circ_6749,RMVar_hsa_circ_103703,RMVar_hsa_circ_289300,RMVar_hsa_circ_4428,RMVar_hsa_circ_216780,RMVar_hsa_circ_216781,RMVar_hsa_circ_216782 43645 RMVar_ID_43645 Human_SNP_ID_128595086 A-to-I Human chr3 - 33541717 33541717 33541717 AATGCCTATCAGTGATAGACTGGATAAAGAAAATGTGGTATCTATACACCATGGAATACTATGTG AATGCCTATCAGTGATAGACTGGATAAAGAAAGTGTGGTATCTATACACCATGGAATACTATGTG T C CLASP2 Ensembl:ENSG00000163539 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1169968606 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14424,RMVar_hsa_circ_113585,RMVar_hsa_circ_304405,RMVar_hsa_circ_21535,RMVar_hsa_circ_46762,RMVar_hsa_circ_24561,RMVar_hsa_circ_2032,RMVar_hsa_circ_27031,RMVar_hsa_circ_61436,RMVar_hsa_circ_216772,RMVar_hsa_circ_286425,RMVar_hsa_circ_365293,RMVar_hsa_circ_265924,RMVar_hsa_circ_42018,RMVar_hsa_circ_6897,RMVar_hsa_circ_216774,RMVar_hsa_circ_326669,RMVar_hsa_circ_365318,RMVar_hsa_circ_286455,RMVar_hsa_circ_111230,RMVar_hsa_circ_120430,RMVar_hsa_circ_101772,RMVar_hsa_circ_216775,RMVar_hsa_circ_216777,RMVar_hsa_circ_216778,RMVar_hsa_circ_216776,RMVar_hsa_circ_6749,RMVar_hsa_circ_103703,RMVar_hsa_circ_4428,RMVar_hsa_circ_54597,RMVar_hsa_circ_335748,RMVar_hsa_circ_216781,RMVar_hsa_circ_216782,RMVar_hsa_circ_340438,RMVar_hsa_circ_314802,RMVar_hsa_circ_316677,RMVar_hsa_circ_304125,RMVar_hsa_circ_115631,RMVar_hsa_circ_285890,RMVar_hsa_circ_74411,RMVar_hsa_circ_216786,RMVar_hsa_circ_45533,RMVar_hsa_circ_216788,RMVar_hsa_circ_6515,RMVar_hsa_circ_216787,RMVar_hsa_circ_309081,RMVar_hsa_circ_216784,RMVar_hsa_circ_216785,RMVar_hsa_circ_355453,RMVar_hsa_circ_216783,RMVar_hsa_circ_328660,RMVar_hsa_circ_269411,RMVar_hsa_circ_272281,RMVar_hsa_circ_267487,RMVar_hsa_circ_216790,RMVar_hsa_circ_216791 43646 RMVar_ID_43646 Human_SNP_ID_128595093 A-to-I Human chr3 - 33541754 33541754 33541754 GCACTGTTCACAATAGCAAAGACATGGAATCAACCTAAATGCCTATCAGTGATAGACTGGATAAA GCACTGTTCACAATAGCAAAGACATGGAATCAGCCTAAATGCCTATCAGTGATAGACTGGATAAA T C CLASP2 Ensembl:ENSG00000163539 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs760602219 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14424,RMVar_hsa_circ_113585,RMVar_hsa_circ_304405,RMVar_hsa_circ_21535,RMVar_hsa_circ_46762,RMVar_hsa_circ_24561,RMVar_hsa_circ_2032,RMVar_hsa_circ_27031,RMVar_hsa_circ_61436,RMVar_hsa_circ_216772,RMVar_hsa_circ_286425,RMVar_hsa_circ_365293,RMVar_hsa_circ_265924,RMVar_hsa_circ_42018,RMVar_hsa_circ_6897,RMVar_hsa_circ_216774,RMVar_hsa_circ_326669,RMVar_hsa_circ_365318,RMVar_hsa_circ_286455,RMVar_hsa_circ_111230,RMVar_hsa_circ_120430,RMVar_hsa_circ_101772,RMVar_hsa_circ_216775,RMVar_hsa_circ_216777,RMVar_hsa_circ_216778,RMVar_hsa_circ_216776,RMVar_hsa_circ_6749,RMVar_hsa_circ_103703,RMVar_hsa_circ_4428,RMVar_hsa_circ_54597,RMVar_hsa_circ_335748,RMVar_hsa_circ_216781,RMVar_hsa_circ_216782,RMVar_hsa_circ_340438,RMVar_hsa_circ_314802,RMVar_hsa_circ_316677,RMVar_hsa_circ_304125,RMVar_hsa_circ_115631,RMVar_hsa_circ_285890,RMVar_hsa_circ_74411,RMVar_hsa_circ_216786,RMVar_hsa_circ_45533,RMVar_hsa_circ_216788,RMVar_hsa_circ_6515,RMVar_hsa_circ_216787,RMVar_hsa_circ_309081,RMVar_hsa_circ_216784,RMVar_hsa_circ_216785,RMVar_hsa_circ_355453,RMVar_hsa_circ_216783,RMVar_hsa_circ_328660,RMVar_hsa_circ_269411,RMVar_hsa_circ_272281,RMVar_hsa_circ_267487,RMVar_hsa_circ_216790,RMVar_hsa_circ_216791 43647 RMVar_ID_43647 Human_SNP_ID_128595133 A-to-I Human chr3 - 33541908 33541908 33541908 ATTAGTTGAACTATTGTGGAAGATAGTGTGGCAATTCCTCAAAGACCTAGAGACAGAAATATAAT ATTAGTTGAACTATTGTGGAAGATAGTGTGGCCATTCCTCAAAGACCTAGAGACAGAAATATAAT T G CLASP2 Ensembl:ENSG00000163539 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs893926422 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14424,RMVar_hsa_circ_113585,RMVar_hsa_circ_304405,RMVar_hsa_circ_21535,RMVar_hsa_circ_46762,RMVar_hsa_circ_24561,RMVar_hsa_circ_2032,RMVar_hsa_circ_27031,RMVar_hsa_circ_61436,RMVar_hsa_circ_216772,RMVar_hsa_circ_286425,RMVar_hsa_circ_365293,RMVar_hsa_circ_265924,RMVar_hsa_circ_42018,RMVar_hsa_circ_6897,RMVar_hsa_circ_216774,RMVar_hsa_circ_326669,RMVar_hsa_circ_365318,RMVar_hsa_circ_286455,RMVar_hsa_circ_111230,RMVar_hsa_circ_120430,RMVar_hsa_circ_101772,RMVar_hsa_circ_216775,RMVar_hsa_circ_216777,RMVar_hsa_circ_216778,RMVar_hsa_circ_216776,RMVar_hsa_circ_6749,RMVar_hsa_circ_103703,RMVar_hsa_circ_4428,RMVar_hsa_circ_54597,RMVar_hsa_circ_335748,RMVar_hsa_circ_216781,RMVar_hsa_circ_216782,RMVar_hsa_circ_340438,RMVar_hsa_circ_314802,RMVar_hsa_circ_316677,RMVar_hsa_circ_304125,RMVar_hsa_circ_115631,RMVar_hsa_circ_285890,RMVar_hsa_circ_74411,RMVar_hsa_circ_216786,RMVar_hsa_circ_45533,RMVar_hsa_circ_216788,RMVar_hsa_circ_6515,RMVar_hsa_circ_216787,RMVar_hsa_circ_309081,RMVar_hsa_circ_216784,RMVar_hsa_circ_216785,RMVar_hsa_circ_355453,RMVar_hsa_circ_216783,RMVar_hsa_circ_328660,RMVar_hsa_circ_269411,RMVar_hsa_circ_272281,RMVar_hsa_circ_267487,RMVar_hsa_circ_216790,RMVar_hsa_circ_216791 43648 RMVar_ID_43648 Human_SNP_ID_128596061 A-to-I Human chr3 - 33545693 33545693 33545693 GTTAGCCAGACTGGTCTCGAACTCCTGACCTCAAGTGATCCACCTGCCTTTGCCTCCCAAAGTGC GTTAGCCAGACTGGTCTCGAACTCCTGACCTCCAGTGATCCACCTGCCTTTGCCTCCCAAAGTGC T G CLASP2 Ensembl:ENSG00000163539 Protein coding intron GSE100210;GSE107867;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;ASD brains,temporal_cortex - 29129909,30559470,30559470 RNA-Seq:(High) rs575396318 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23022581 RMVar_hsa_circ_14424,RMVar_hsa_circ_113585,RMVar_hsa_circ_21535,RMVar_hsa_circ_46762,RMVar_hsa_circ_24561,RMVar_hsa_circ_2032,RMVar_hsa_circ_27031,RMVar_hsa_circ_61436,RMVar_hsa_circ_216772,RMVar_hsa_circ_365293,RMVar_hsa_circ_265924,RMVar_hsa_circ_42018,RMVar_hsa_circ_6897,RMVar_hsa_circ_365318,RMVar_hsa_circ_286455,RMVar_hsa_circ_111230,RMVar_hsa_circ_120430,RMVar_hsa_circ_101772,RMVar_hsa_circ_216775,RMVar_hsa_circ_216777,RMVar_hsa_circ_216778,RMVar_hsa_circ_216776,RMVar_hsa_circ_6749,RMVar_hsa_circ_103703,RMVar_hsa_circ_54597,RMVar_hsa_circ_335748,RMVar_hsa_circ_216781,RMVar_hsa_circ_216782,RMVar_hsa_circ_340438,RMVar_hsa_circ_314802,RMVar_hsa_circ_304125,RMVar_hsa_circ_115631,RMVar_hsa_circ_285890,RMVar_hsa_circ_74411,RMVar_hsa_circ_216786,RMVar_hsa_circ_45533,RMVar_hsa_circ_6515,RMVar_hsa_circ_216787,RMVar_hsa_circ_309081,RMVar_hsa_circ_216784,RMVar_hsa_circ_216785,RMVar_hsa_circ_355453,RMVar_hsa_circ_216783,RMVar_hsa_circ_328660,RMVar_hsa_circ_269411,RMVar_hsa_circ_272281,RMVar_hsa_circ_267487,RMVar_hsa_circ_40304,RMVar_hsa_circ_216790,RMVar_hsa_circ_216791,RMVar_hsa_circ_280203,RMVar_hsa_circ_284113,RMVar_hsa_circ_307670,RMVar_hsa_circ_269553,RMVar_hsa_circ_24442,RMVar_hsa_circ_20980,RMVar_hsa_circ_216794,RMVar_hsa_circ_216795,RMVar_hsa_circ_216793,RMVar_hsa_circ_268213,RMVar_hsa_circ_372053,RMVar_hsa_circ_216796 43649 RMVar_ID_43649 Human_SNP_ID_128596102 A-to-I Human chr3 - 33545866 33545866 33545866 TCACTTTGTCTCCCAGGCTGGAGTGCAGTGGCATGATCTCTGCTCACTGCAACTTCTGCCTCCCA TCACTTTGTCTCCCAGGCTGGAGTGCAGTGGCGTGATCTCTGCTCACTGCAACTTCTGCCTCCCA T C CLASP2 Ensembl:ENSG00000163539 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs950436754 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14424,RMVar_hsa_circ_113585,RMVar_hsa_circ_21535,RMVar_hsa_circ_46762,RMVar_hsa_circ_24561,RMVar_hsa_circ_2032,RMVar_hsa_circ_27031,RMVar_hsa_circ_61436,RMVar_hsa_circ_216772,RMVar_hsa_circ_365293,RMVar_hsa_circ_265924,RMVar_hsa_circ_42018,RMVar_hsa_circ_6897,RMVar_hsa_circ_365318,RMVar_hsa_circ_286455,RMVar_hsa_circ_111230,RMVar_hsa_circ_120430,RMVar_hsa_circ_101772,RMVar_hsa_circ_216775,RMVar_hsa_circ_216777,RMVar_hsa_circ_216778,RMVar_hsa_circ_216776,RMVar_hsa_circ_6749,RMVar_hsa_circ_103703,RMVar_hsa_circ_54597,RMVar_hsa_circ_335748,RMVar_hsa_circ_216781,RMVar_hsa_circ_216782,RMVar_hsa_circ_340438,RMVar_hsa_circ_314802,RMVar_hsa_circ_304125,RMVar_hsa_circ_115631,RMVar_hsa_circ_285890,RMVar_hsa_circ_74411,RMVar_hsa_circ_216786,RMVar_hsa_circ_45533,RMVar_hsa_circ_6515,RMVar_hsa_circ_216787,RMVar_hsa_circ_309081,RMVar_hsa_circ_216784,RMVar_hsa_circ_216785,RMVar_hsa_circ_355453,RMVar_hsa_circ_216783,RMVar_hsa_circ_328660,RMVar_hsa_circ_269411,RMVar_hsa_circ_272281,RMVar_hsa_circ_267487,RMVar_hsa_circ_40304,RMVar_hsa_circ_216790,RMVar_hsa_circ_216791,RMVar_hsa_circ_280203,RMVar_hsa_circ_284113,RMVar_hsa_circ_307670,RMVar_hsa_circ_269553,RMVar_hsa_circ_24442,RMVar_hsa_circ_20980,RMVar_hsa_circ_216794,RMVar_hsa_circ_216795,RMVar_hsa_circ_216793,RMVar_hsa_circ_268213,RMVar_hsa_circ_372053,RMVar_hsa_circ_216796 43650 RMVar_ID_43650 Human_SNP_ID_128596560 A-to-I Human chr3 - 33547860 33547860 33547860 CATTTGAGTCTGGGAGGTCGATGCTGCAGTGAACTGTGATTACACCACTGCACTCCAGCCCGAGT CATTTGAGTCTGGGAGGTCGATGCTGCAGTGAGCTGTGATTACACCACTGCACTCCAGCCCGAGT T C CLASP2 Ensembl:ENSG00000163539 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1322913303 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9139644 RMVar_hsa_circ_14424,RMVar_hsa_circ_113585,RMVar_hsa_circ_21535,RMVar_hsa_circ_46762,RMVar_hsa_circ_24561,RMVar_hsa_circ_2032,RMVar_hsa_circ_27031,RMVar_hsa_circ_61436,RMVar_hsa_circ_216772,RMVar_hsa_circ_365293,RMVar_hsa_circ_265924,RMVar_hsa_circ_42018,RMVar_hsa_circ_6897,RMVar_hsa_circ_365318,RMVar_hsa_circ_286455,RMVar_hsa_circ_111230,RMVar_hsa_circ_120430,RMVar_hsa_circ_101772,RMVar_hsa_circ_216775,RMVar_hsa_circ_216777,RMVar_hsa_circ_216778,RMVar_hsa_circ_216776,RMVar_hsa_circ_6749,RMVar_hsa_circ_103703,RMVar_hsa_circ_54597,RMVar_hsa_circ_335748,RMVar_hsa_circ_216781,RMVar_hsa_circ_216782,RMVar_hsa_circ_340438,RMVar_hsa_circ_314802,RMVar_hsa_circ_304125,RMVar_hsa_circ_115631,RMVar_hsa_circ_285890,RMVar_hsa_circ_74411,RMVar_hsa_circ_216786,RMVar_hsa_circ_45533,RMVar_hsa_circ_6515,RMVar_hsa_circ_216787,RMVar_hsa_circ_309081,RMVar_hsa_circ_216784,RMVar_hsa_circ_216785,RMVar_hsa_circ_355453,RMVar_hsa_circ_216783,RMVar_hsa_circ_328660,RMVar_hsa_circ_269411,RMVar_hsa_circ_272281,RMVar_hsa_circ_267487,RMVar_hsa_circ_40304,RMVar_hsa_circ_216790,RMVar_hsa_circ_216791,RMVar_hsa_circ_280203,RMVar_hsa_circ_284113,RMVar_hsa_circ_307670,RMVar_hsa_circ_269553,RMVar_hsa_circ_24442,RMVar_hsa_circ_20980,RMVar_hsa_circ_216794,RMVar_hsa_circ_216795,RMVar_hsa_circ_216793,RMVar_hsa_circ_268213,RMVar_hsa_circ_372053,RMVar_hsa_circ_216796 43651 RMVar_ID_43651 Human_SNP_ID_128596573 A-to-I Human chr3 - 33547913 33547913 33547913 GTGGTGGCATACACCTGTAGTCCCAGCTACTCAGGAGGCTGAGGTAGGAGGATCATTTGAGTCTG GTGGTGGCATACACCTGTAGTCCCAGCTACTCGGGAGGCTGAGGTAGGAGGATCATTTGAGTCTG T C CLASP2 Ensembl:ENSG00000163539 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1489534773 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_212630 RMVar_hsa_circ_14424,RMVar_hsa_circ_113585,RMVar_hsa_circ_21535,RMVar_hsa_circ_46762,RMVar_hsa_circ_24561,RMVar_hsa_circ_2032,RMVar_hsa_circ_27031,RMVar_hsa_circ_61436,RMVar_hsa_circ_216772,RMVar_hsa_circ_365293,RMVar_hsa_circ_265924,RMVar_hsa_circ_42018,RMVar_hsa_circ_6897,RMVar_hsa_circ_365318,RMVar_hsa_circ_286455,RMVar_hsa_circ_111230,RMVar_hsa_circ_120430,RMVar_hsa_circ_101772,RMVar_hsa_circ_216775,RMVar_hsa_circ_216777,RMVar_hsa_circ_216778,RMVar_hsa_circ_216776,RMVar_hsa_circ_6749,RMVar_hsa_circ_103703,RMVar_hsa_circ_54597,RMVar_hsa_circ_335748,RMVar_hsa_circ_216781,RMVar_hsa_circ_216782,RMVar_hsa_circ_340438,RMVar_hsa_circ_314802,RMVar_hsa_circ_304125,RMVar_hsa_circ_115631,RMVar_hsa_circ_285890,RMVar_hsa_circ_74411,RMVar_hsa_circ_216786,RMVar_hsa_circ_45533,RMVar_hsa_circ_6515,RMVar_hsa_circ_216787,RMVar_hsa_circ_309081,RMVar_hsa_circ_216784,RMVar_hsa_circ_216785,RMVar_hsa_circ_355453,RMVar_hsa_circ_216783,RMVar_hsa_circ_328660,RMVar_hsa_circ_269411,RMVar_hsa_circ_272281,RMVar_hsa_circ_267487,RMVar_hsa_circ_40304,RMVar_hsa_circ_216790,RMVar_hsa_circ_216791,RMVar_hsa_circ_280203,RMVar_hsa_circ_284113,RMVar_hsa_circ_307670,RMVar_hsa_circ_269553,RMVar_hsa_circ_24442,RMVar_hsa_circ_20980,RMVar_hsa_circ_216794,RMVar_hsa_circ_216795,RMVar_hsa_circ_216793,RMVar_hsa_circ_268213,RMVar_hsa_circ_372053,RMVar_hsa_circ_216796 43652 RMVar_ID_43652 Human_SNP_ID_128596691 A-to-I Human chr3 - 33548422 33548422 33548422 GTGGTGGCACGCACCTGCAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATGGCTTGAACCTG GTGGTGGCACGCACCTGCAGTCCCAGCTACTCTGGAGGCTGAGGCAGGAGAATGGCTTGAACCTG T A CLASP2 Ensembl:ENSG00000163539 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1190722359 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14424,RMVar_hsa_circ_113585,RMVar_hsa_circ_21535,RMVar_hsa_circ_46762,RMVar_hsa_circ_24561,RMVar_hsa_circ_2032,RMVar_hsa_circ_27031,RMVar_hsa_circ_61436,RMVar_hsa_circ_216772,RMVar_hsa_circ_365293,RMVar_hsa_circ_265924,RMVar_hsa_circ_42018,RMVar_hsa_circ_6897,RMVar_hsa_circ_365318,RMVar_hsa_circ_286455,RMVar_hsa_circ_111230,RMVar_hsa_circ_120430,RMVar_hsa_circ_101772,RMVar_hsa_circ_216775,RMVar_hsa_circ_216777,RMVar_hsa_circ_216778,RMVar_hsa_circ_216776,RMVar_hsa_circ_6749,RMVar_hsa_circ_103703,RMVar_hsa_circ_54597,RMVar_hsa_circ_335748,RMVar_hsa_circ_216781,RMVar_hsa_circ_216782,RMVar_hsa_circ_340438,RMVar_hsa_circ_314802,RMVar_hsa_circ_304125,RMVar_hsa_circ_115631,RMVar_hsa_circ_285890,RMVar_hsa_circ_74411,RMVar_hsa_circ_216786,RMVar_hsa_circ_45533,RMVar_hsa_circ_6515,RMVar_hsa_circ_216787,RMVar_hsa_circ_309081,RMVar_hsa_circ_216784,RMVar_hsa_circ_216785,RMVar_hsa_circ_355453,RMVar_hsa_circ_216783,RMVar_hsa_circ_328660,RMVar_hsa_circ_269411,RMVar_hsa_circ_272281,RMVar_hsa_circ_267487,RMVar_hsa_circ_40304,RMVar_hsa_circ_216790,RMVar_hsa_circ_216791,RMVar_hsa_circ_280203,RMVar_hsa_circ_284113,RMVar_hsa_circ_307670,RMVar_hsa_circ_269553,RMVar_hsa_circ_24442,RMVar_hsa_circ_20980,RMVar_hsa_circ_216794,RMVar_hsa_circ_216795,RMVar_hsa_circ_216793,RMVar_hsa_circ_268213,RMVar_hsa_circ_372053,RMVar_hsa_circ_216796 43653 RMVar_ID_43653 Human_SNP_ID_128596861 A-to-I Human chr3 - 33548924 33548924 33548924 TGCAAAAAAAGAAAATTCAAAATTAGGTGGGTATGGTGGTGCATGCCTGTAGTCCCAGATACTCA TGCAAAAAAAGAAAATTCAAAATTAGGTGGGTGTGGTGGTGCATGCCTGTAGTCCCAGATACTCA T C CLASP2 Ensembl:ENSG00000163539 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs922702031 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14796603 RMVar_hsa_circ_14424,RMVar_hsa_circ_113585,RMVar_hsa_circ_21535,RMVar_hsa_circ_46762,RMVar_hsa_circ_24561,RMVar_hsa_circ_2032,RMVar_hsa_circ_27031,RMVar_hsa_circ_61436,RMVar_hsa_circ_216772,RMVar_hsa_circ_365293,RMVar_hsa_circ_265924,RMVar_hsa_circ_42018,RMVar_hsa_circ_6897,RMVar_hsa_circ_365318,RMVar_hsa_circ_286455,RMVar_hsa_circ_111230,RMVar_hsa_circ_120430,RMVar_hsa_circ_101772,RMVar_hsa_circ_216775,RMVar_hsa_circ_216777,RMVar_hsa_circ_216778,RMVar_hsa_circ_216776,RMVar_hsa_circ_6749,RMVar_hsa_circ_103703,RMVar_hsa_circ_54597,RMVar_hsa_circ_335748,RMVar_hsa_circ_216781,RMVar_hsa_circ_216782,RMVar_hsa_circ_340438,RMVar_hsa_circ_314802,RMVar_hsa_circ_304125,RMVar_hsa_circ_115631,RMVar_hsa_circ_285890,RMVar_hsa_circ_74411,RMVar_hsa_circ_216786,RMVar_hsa_circ_45533,RMVar_hsa_circ_6515,RMVar_hsa_circ_216787,RMVar_hsa_circ_309081,RMVar_hsa_circ_216784,RMVar_hsa_circ_216785,RMVar_hsa_circ_355453,RMVar_hsa_circ_216783,RMVar_hsa_circ_328660,RMVar_hsa_circ_269411,RMVar_hsa_circ_272281,RMVar_hsa_circ_267487,RMVar_hsa_circ_40304,RMVar_hsa_circ_216790,RMVar_hsa_circ_216791,RMVar_hsa_circ_280203,RMVar_hsa_circ_284113,RMVar_hsa_circ_307670,RMVar_hsa_circ_269553,RMVar_hsa_circ_24442,RMVar_hsa_circ_20980,RMVar_hsa_circ_216794,RMVar_hsa_circ_216795,RMVar_hsa_circ_216793,RMVar_hsa_circ_268213,RMVar_hsa_circ_372053,RMVar_hsa_circ_216796 43654 RMVar_ID_43654 Human_SNP_ID_128597208 A-to-I Human chr3 - 33550351 33550351 33550351 TCGCTTTTTCACCCAGGCTGGAGCACAGTGGCATGATACTGGCTCACTGCAACCTCCACCTTCCA TCGCTTTTTCACCCAGGCTGGAGCACAGTGGCGTGATACTGGCTCACTGCAACCTCCACCTTCCA T C CLASP2 Ensembl:ENSG00000163539 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs904009360 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14796625 RMVar_hsa_circ_14424,RMVar_hsa_circ_113585,RMVar_hsa_circ_21535,RMVar_hsa_circ_46762,RMVar_hsa_circ_24561,RMVar_hsa_circ_2032,RMVar_hsa_circ_27031,RMVar_hsa_circ_61436,RMVar_hsa_circ_216772,RMVar_hsa_circ_365293,RMVar_hsa_circ_265924,RMVar_hsa_circ_42018,RMVar_hsa_circ_6897,RMVar_hsa_circ_365318,RMVar_hsa_circ_286455,RMVar_hsa_circ_111230,RMVar_hsa_circ_120430,RMVar_hsa_circ_101772,RMVar_hsa_circ_216775,RMVar_hsa_circ_216777,RMVar_hsa_circ_216778,RMVar_hsa_circ_216776,RMVar_hsa_circ_6749,RMVar_hsa_circ_103703,RMVar_hsa_circ_54597,RMVar_hsa_circ_335748,RMVar_hsa_circ_216781,RMVar_hsa_circ_216782,RMVar_hsa_circ_340438,RMVar_hsa_circ_314802,RMVar_hsa_circ_304125,RMVar_hsa_circ_115631,RMVar_hsa_circ_285890,RMVar_hsa_circ_74411,RMVar_hsa_circ_216786,RMVar_hsa_circ_45533,RMVar_hsa_circ_6515,RMVar_hsa_circ_216787,RMVar_hsa_circ_309081,RMVar_hsa_circ_216784,RMVar_hsa_circ_216785,RMVar_hsa_circ_355453,RMVar_hsa_circ_216783,RMVar_hsa_circ_328660,RMVar_hsa_circ_269411,RMVar_hsa_circ_272281,RMVar_hsa_circ_267487,RMVar_hsa_circ_40304,RMVar_hsa_circ_216790,RMVar_hsa_circ_216791,RMVar_hsa_circ_280203,RMVar_hsa_circ_284113,RMVar_hsa_circ_307670,RMVar_hsa_circ_269553,RMVar_hsa_circ_24442,RMVar_hsa_circ_20980,RMVar_hsa_circ_216794,RMVar_hsa_circ_216795,RMVar_hsa_circ_216793,RMVar_hsa_circ_268213,RMVar_hsa_circ_372053,RMVar_hsa_circ_216796 43655 RMVar_ID_43655 Human_SNP_ID_128613185 A-to-I Human chr3 - 33614882 33614882 33614882 GGTTCAAGCTATTCTTCTGCCTCAGCCTCCCAAGTAGCTGGGCTTTCAGGCACCTGCCACCACGC GGTTCAAGCTATTCTTCTGCCTCAGCCTCCCAGGTAGCTGGGCTTTCAGGCACCTGCCACCACGC T C CLASP2 Ensembl:ENSG00000163539 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs940118029 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120430,RMVar_hsa_circ_216775,RMVar_hsa_circ_54597,RMVar_hsa_circ_45533,RMVar_hsa_circ_309081,RMVar_hsa_circ_17296,RMVar_hsa_circ_45931,RMVar_hsa_circ_11458,RMVar_hsa_circ_887,RMVar_hsa_circ_670,RMVar_hsa_circ_216807,RMVar_hsa_circ_85253,RMVar_hsa_circ_216813,RMVar_hsa_circ_343818,RMVar_hsa_circ_378220,RMVar_hsa_circ_55048,RMVar_hsa_circ_216816,RMVar_hsa_circ_216815,RMVar_hsa_circ_348981,RMVar_hsa_circ_57250,RMVar_hsa_circ_327791,RMVar_hsa_circ_281120,RMVar_hsa_circ_89016,RMVar_hsa_circ_216826,RMVar_hsa_circ_91930,RMVar_hsa_circ_216825,RMVar_hsa_circ_5418,RMVar_hsa_circ_216824,RMVar_hsa_circ_375783,RMVar_hsa_circ_216827,RMVar_hsa_circ_292790,RMVar_hsa_circ_343394,RMVar_hsa_circ_216829,RMVar_hsa_circ_93377,RMVar_hsa_circ_216828,RMVar_hsa_circ_358024,RMVar_hsa_circ_301402,RMVar_hsa_circ_297056,RMVar_hsa_circ_121793,RMVar_hsa_circ_112038,RMVar_hsa_circ_216830,RMVar_hsa_circ_24946,RMVar_hsa_circ_28869,RMVar_hsa_circ_216832,RMVar_hsa_circ_216834,RMVar_hsa_circ_216835,RMVar_hsa_circ_216833,RMVar_hsa_circ_216831,RMVar_hsa_circ_13077,RMVar_hsa_circ_15268,RMVar_hsa_circ_216840,RMVar_hsa_circ_320151,RMVar_hsa_circ_330328,RMVar_hsa_circ_316663,RMVar_hsa_circ_285869,RMVar_hsa_circ_295885,RMVar_hsa_circ_24156,RMVar_hsa_circ_216841,RMVar_hsa_circ_216838,RMVar_hsa_circ_216839,RMVar_hsa_circ_295870,RMVar_hsa_circ_216837,RMVar_hsa_circ_274177,RMVar_hsa_circ_125096,RMVar_hsa_circ_216845,RMVar_hsa_circ_216846,RMVar_hsa_circ_216847,RMVar_hsa_circ_216849,RMVar_hsa_circ_216851,RMVar_hsa_circ_282580,RMVar_hsa_circ_357907,RMVar_hsa_circ_216848,RMVar_hsa_circ_313784,RMVar_hsa_circ_278587,RMVar_hsa_circ_216850 43656 RMVar_ID_43656 Human_SNP_ID_128613689 A-to-I Human chr3 - 33616843 33616842 33616843 ATCCCAGCTACTCTGGAGGCTGAGGCAGGAGTATTGCTTGAACTTGGGAGGGGGAGGTTGCAGTG ATCCCAGCTACTCTGGAGGCTGAGGCAGGAGT_TTGCTTGAACTTGGGAGGGGGAGGTTGCAGTG AT A CLASP2 Ensembl:ENSG00000163539 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1307890356 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_120430,RMVar_hsa_circ_216775,RMVar_hsa_circ_54597,RMVar_hsa_circ_45533,RMVar_hsa_circ_309081,RMVar_hsa_circ_17296,RMVar_hsa_circ_45931,RMVar_hsa_circ_11458,RMVar_hsa_circ_887,RMVar_hsa_circ_670,RMVar_hsa_circ_216807,RMVar_hsa_circ_85253,RMVar_hsa_circ_216813,RMVar_hsa_circ_343818,RMVar_hsa_circ_378220,RMVar_hsa_circ_55048,RMVar_hsa_circ_216816,RMVar_hsa_circ_216815,RMVar_hsa_circ_348981,RMVar_hsa_circ_57250,RMVar_hsa_circ_327791,RMVar_hsa_circ_281120,RMVar_hsa_circ_89016,RMVar_hsa_circ_216826,RMVar_hsa_circ_91930,RMVar_hsa_circ_216825,RMVar_hsa_circ_5418,RMVar_hsa_circ_216824,RMVar_hsa_circ_375783,RMVar_hsa_circ_216827,RMVar_hsa_circ_292790,RMVar_hsa_circ_343394,RMVar_hsa_circ_216829,RMVar_hsa_circ_93377,RMVar_hsa_circ_216828,RMVar_hsa_circ_358024,RMVar_hsa_circ_301402,RMVar_hsa_circ_297056,RMVar_hsa_circ_121793,RMVar_hsa_circ_112038,RMVar_hsa_circ_216830,RMVar_hsa_circ_24946,RMVar_hsa_circ_28869,RMVar_hsa_circ_216832,RMVar_hsa_circ_216834,RMVar_hsa_circ_216835,RMVar_hsa_circ_216833,RMVar_hsa_circ_216831,RMVar_hsa_circ_13077,RMVar_hsa_circ_15268,RMVar_hsa_circ_216840,RMVar_hsa_circ_320151,RMVar_hsa_circ_330328,RMVar_hsa_circ_316663,RMVar_hsa_circ_285869,RMVar_hsa_circ_295885,RMVar_hsa_circ_24156,RMVar_hsa_circ_216841,RMVar_hsa_circ_216838,RMVar_hsa_circ_216839,RMVar_hsa_circ_295870,RMVar_hsa_circ_216837,RMVar_hsa_circ_274177,RMVar_hsa_circ_125096,RMVar_hsa_circ_216845,RMVar_hsa_circ_216846,RMVar_hsa_circ_216847,RMVar_hsa_circ_216849,RMVar_hsa_circ_216851,RMVar_hsa_circ_282580,RMVar_hsa_circ_357907,RMVar_hsa_circ_216848,RMVar_hsa_circ_313784,RMVar_hsa_circ_278587,RMVar_hsa_circ_216850 43657 RMVar_ID_43657 Human_SNP_ID_128613715 A-to-I Human chr3 - 33616959 33616959 33616959 TGGGAGGCTGAGGCAGGTCGATCACAGGAGTCAAGACCAGCCAGGCCAATATGGTGAAACCCCAT TGGGAGGCTGAGGCAGGTCGATCACAGGAGTCGAGACCAGCCAGGCCAATATGGTGAAACCCCAT T C CLASP2 Ensembl:ENSG00000163539 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs898761727 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7189292 RMVar_hsa_circ_120430,RMVar_hsa_circ_216775,RMVar_hsa_circ_54597,RMVar_hsa_circ_45533,RMVar_hsa_circ_309081,RMVar_hsa_circ_17296,RMVar_hsa_circ_45931,RMVar_hsa_circ_11458,RMVar_hsa_circ_887,RMVar_hsa_circ_670,RMVar_hsa_circ_216807,RMVar_hsa_circ_85253,RMVar_hsa_circ_216813,RMVar_hsa_circ_343818,RMVar_hsa_circ_378220,RMVar_hsa_circ_55048,RMVar_hsa_circ_216816,RMVar_hsa_circ_216815,RMVar_hsa_circ_348981,RMVar_hsa_circ_57250,RMVar_hsa_circ_327791,RMVar_hsa_circ_281120,RMVar_hsa_circ_89016,RMVar_hsa_circ_216826,RMVar_hsa_circ_91930,RMVar_hsa_circ_216825,RMVar_hsa_circ_5418,RMVar_hsa_circ_216824,RMVar_hsa_circ_375783,RMVar_hsa_circ_216827,RMVar_hsa_circ_292790,RMVar_hsa_circ_343394,RMVar_hsa_circ_216829,RMVar_hsa_circ_93377,RMVar_hsa_circ_216828,RMVar_hsa_circ_358024,RMVar_hsa_circ_301402,RMVar_hsa_circ_297056,RMVar_hsa_circ_121793,RMVar_hsa_circ_112038,RMVar_hsa_circ_216830,RMVar_hsa_circ_24946,RMVar_hsa_circ_28869,RMVar_hsa_circ_216832,RMVar_hsa_circ_216834,RMVar_hsa_circ_216835,RMVar_hsa_circ_216833,RMVar_hsa_circ_216831,RMVar_hsa_circ_13077,RMVar_hsa_circ_15268,RMVar_hsa_circ_216840,RMVar_hsa_circ_320151,RMVar_hsa_circ_330328,RMVar_hsa_circ_316663,RMVar_hsa_circ_285869,RMVar_hsa_circ_295885,RMVar_hsa_circ_24156,RMVar_hsa_circ_216841,RMVar_hsa_circ_216838,RMVar_hsa_circ_216839,RMVar_hsa_circ_295870,RMVar_hsa_circ_216837,RMVar_hsa_circ_274177,RMVar_hsa_circ_125096,RMVar_hsa_circ_216845,RMVar_hsa_circ_216846,RMVar_hsa_circ_216847,RMVar_hsa_circ_216849,RMVar_hsa_circ_216851,RMVar_hsa_circ_282580,RMVar_hsa_circ_357907,RMVar_hsa_circ_216848,RMVar_hsa_circ_313784,RMVar_hsa_circ_278587,RMVar_hsa_circ_216850 43658 RMVar_ID_43658 Human_SNP_ID_128614026 A-to-I Human chr3 - 33618086 33618086 33618086 AAATTAGCCAGGCATGGTGGCGCATGCCTGTAATCCCAGCCGCTCGGGAAGCTGAGGCAGGAGAA AAATTAGCCAGGCATGGTGGCGCATGCCTGTAGTCCCAGCCGCTCGGGAAGCTGAGGCAGGAGAA T C CLASP2 Ensembl:ENSG00000163539 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1479148300 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120430,RMVar_hsa_circ_216775,RMVar_hsa_circ_54597,RMVar_hsa_circ_45533,RMVar_hsa_circ_309081,RMVar_hsa_circ_17296,RMVar_hsa_circ_45931,RMVar_hsa_circ_11458,RMVar_hsa_circ_887,RMVar_hsa_circ_670,RMVar_hsa_circ_216807,RMVar_hsa_circ_85253,RMVar_hsa_circ_216813,RMVar_hsa_circ_343818,RMVar_hsa_circ_378220,RMVar_hsa_circ_55048,RMVar_hsa_circ_216816,RMVar_hsa_circ_216815,RMVar_hsa_circ_348981,RMVar_hsa_circ_57250,RMVar_hsa_circ_327791,RMVar_hsa_circ_281120,RMVar_hsa_circ_89016,RMVar_hsa_circ_216826,RMVar_hsa_circ_91930,RMVar_hsa_circ_216825,RMVar_hsa_circ_5418,RMVar_hsa_circ_216824,RMVar_hsa_circ_375783,RMVar_hsa_circ_216827,RMVar_hsa_circ_292790,RMVar_hsa_circ_343394,RMVar_hsa_circ_216829,RMVar_hsa_circ_93377,RMVar_hsa_circ_216828,RMVar_hsa_circ_358024,RMVar_hsa_circ_301402,RMVar_hsa_circ_297056,RMVar_hsa_circ_121793,RMVar_hsa_circ_112038,RMVar_hsa_circ_216830,RMVar_hsa_circ_24946,RMVar_hsa_circ_28869,RMVar_hsa_circ_216832,RMVar_hsa_circ_216834,RMVar_hsa_circ_216835,RMVar_hsa_circ_216833,RMVar_hsa_circ_216831,RMVar_hsa_circ_13077,RMVar_hsa_circ_15268,RMVar_hsa_circ_216840,RMVar_hsa_circ_320151,RMVar_hsa_circ_330328,RMVar_hsa_circ_316663,RMVar_hsa_circ_285869,RMVar_hsa_circ_295885,RMVar_hsa_circ_24156,RMVar_hsa_circ_216841,RMVar_hsa_circ_216838,RMVar_hsa_circ_216839,RMVar_hsa_circ_295870,RMVar_hsa_circ_216837,RMVar_hsa_circ_274177,RMVar_hsa_circ_125096,RMVar_hsa_circ_216845,RMVar_hsa_circ_216846,RMVar_hsa_circ_216847,RMVar_hsa_circ_216849,RMVar_hsa_circ_216851,RMVar_hsa_circ_282580,RMVar_hsa_circ_357907,RMVar_hsa_circ_216848,RMVar_hsa_circ_313784,RMVar_hsa_circ_278587,RMVar_hsa_circ_216850 43659 RMVar_ID_43659 Human_SNP_ID_128614116 A-to-I Human chr3 - 33618463 33618463 33618463 TTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCCAGGCTGGTCTCAAACCCCTGGCT TTTTGTATTTTTAGTAGAGACAGGGTTTCACCGTGTTGGCCCAGGCTGGTCTCAAACCCCTGGCT T C CLASP2 Ensembl:ENSG00000163539 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1344764290 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25733569 RMVar_hsa_circ_120430,RMVar_hsa_circ_216775,RMVar_hsa_circ_54597,RMVar_hsa_circ_45533,RMVar_hsa_circ_309081,RMVar_hsa_circ_17296,RMVar_hsa_circ_45931,RMVar_hsa_circ_11458,RMVar_hsa_circ_887,RMVar_hsa_circ_670,RMVar_hsa_circ_216807,RMVar_hsa_circ_85253,RMVar_hsa_circ_216813,RMVar_hsa_circ_343818,RMVar_hsa_circ_378220,RMVar_hsa_circ_55048,RMVar_hsa_circ_216816,RMVar_hsa_circ_216815,RMVar_hsa_circ_348981,RMVar_hsa_circ_57250,RMVar_hsa_circ_327791,RMVar_hsa_circ_281120,RMVar_hsa_circ_89016,RMVar_hsa_circ_216826,RMVar_hsa_circ_91930,RMVar_hsa_circ_216825,RMVar_hsa_circ_5418,RMVar_hsa_circ_216824,RMVar_hsa_circ_375783,RMVar_hsa_circ_216827,RMVar_hsa_circ_292790,RMVar_hsa_circ_343394,RMVar_hsa_circ_216829,RMVar_hsa_circ_93377,RMVar_hsa_circ_216828,RMVar_hsa_circ_358024,RMVar_hsa_circ_301402,RMVar_hsa_circ_297056,RMVar_hsa_circ_121793,RMVar_hsa_circ_112038,RMVar_hsa_circ_216830,RMVar_hsa_circ_24946,RMVar_hsa_circ_28869,RMVar_hsa_circ_216832,RMVar_hsa_circ_216834,RMVar_hsa_circ_216835,RMVar_hsa_circ_216833,RMVar_hsa_circ_216831,RMVar_hsa_circ_13077,RMVar_hsa_circ_15268,RMVar_hsa_circ_216840,RMVar_hsa_circ_320151,RMVar_hsa_circ_330328,RMVar_hsa_circ_316663,RMVar_hsa_circ_285869,RMVar_hsa_circ_295885,RMVar_hsa_circ_24156,RMVar_hsa_circ_216841,RMVar_hsa_circ_216838,RMVar_hsa_circ_216839,RMVar_hsa_circ_295870,RMVar_hsa_circ_216837,RMVar_hsa_circ_274177,RMVar_hsa_circ_125096,RMVar_hsa_circ_216845,RMVar_hsa_circ_216846,RMVar_hsa_circ_216847,RMVar_hsa_circ_216849,RMVar_hsa_circ_216851,RMVar_hsa_circ_282580,RMVar_hsa_circ_357907,RMVar_hsa_circ_216848,RMVar_hsa_circ_313784,RMVar_hsa_circ_278587,RMVar_hsa_circ_216850 43660 RMVar_ID_43660 Human_SNP_ID_128618393 A-to-I Human chr3 - 33637288 33637288 33637288 ACCTCCAGTGATCCGCCTGCCTTGGCCTTCCAAAGTGCTGGGATTACAGACGTGAGCCACCACAC ACCTCCAGTGATCCGCCTGCCTTGGCCTTCCAGAGTGCTGGGATTACAGACGTGAGCCACCACAC T C CLASP2 Ensembl:ENSG00000163539 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1175535582 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120430,RMVar_hsa_circ_216775,RMVar_hsa_circ_54597,RMVar_hsa_circ_17296,RMVar_hsa_circ_887,RMVar_hsa_circ_670,RMVar_hsa_circ_216807,RMVar_hsa_circ_85253,RMVar_hsa_circ_216813,RMVar_hsa_circ_378220,RMVar_hsa_circ_216816,RMVar_hsa_circ_216815,RMVar_hsa_circ_57250,RMVar_hsa_circ_281120,RMVar_hsa_circ_89016,RMVar_hsa_circ_216825,RMVar_hsa_circ_375783,RMVar_hsa_circ_216827,RMVar_hsa_circ_216829,RMVar_hsa_circ_93377,RMVar_hsa_circ_216828,RMVar_hsa_circ_358024,RMVar_hsa_circ_301402,RMVar_hsa_circ_121793,RMVar_hsa_circ_112038,RMVar_hsa_circ_216830,RMVar_hsa_circ_24946,RMVar_hsa_circ_216832,RMVar_hsa_circ_216833,RMVar_hsa_circ_216831,RMVar_hsa_circ_104839,RMVar_hsa_circ_285869,RMVar_hsa_circ_295885,RMVar_hsa_circ_24156,RMVar_hsa_circ_216838,RMVar_hsa_circ_216837,RMVar_hsa_circ_125096,RMVar_hsa_circ_216847,RMVar_hsa_circ_216849,RMVar_hsa_circ_357907,RMVar_hsa_circ_216848,RMVar_hsa_circ_278587,RMVar_hsa_circ_288237,RMVar_hsa_circ_313351,RMVar_hsa_circ_273655,RMVar_hsa_circ_216858,RMVar_hsa_circ_216859,RMVar_hsa_circ_216860,RMVar_hsa_circ_216857,RMVar_hsa_circ_115061,RMVar_hsa_circ_26272,RMVar_hsa_circ_322781,RMVar_hsa_circ_314740,RMVar_hsa_circ_351751,RMVar_hsa_circ_216861,RMVar_hsa_circ_348274,RMVar_hsa_circ_216862 43661 RMVar_ID_43661 Human_SNP_ID_128618416 A-to-I Human chr3 - 33637425 33637425 33637425 GGTTCAAGCGATTCTCCTGCCTCGGCCTTTCAAGTAGCTGGGACTACAGTTGCCTGCCACCACCA GGTTCAAGCGATTCTCCTGCCTCGGCCTTTCAGGTAGCTGGGACTACAGTTGCCTGCCACCACCA T C CLASP2 Ensembl:ENSG00000163539 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs951814062 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120430,RMVar_hsa_circ_216775,RMVar_hsa_circ_54597,RMVar_hsa_circ_17296,RMVar_hsa_circ_887,RMVar_hsa_circ_670,RMVar_hsa_circ_216807,RMVar_hsa_circ_85253,RMVar_hsa_circ_216813,RMVar_hsa_circ_378220,RMVar_hsa_circ_216816,RMVar_hsa_circ_216815,RMVar_hsa_circ_57250,RMVar_hsa_circ_281120,RMVar_hsa_circ_89016,RMVar_hsa_circ_216825,RMVar_hsa_circ_375783,RMVar_hsa_circ_216827,RMVar_hsa_circ_216829,RMVar_hsa_circ_93377,RMVar_hsa_circ_216828,RMVar_hsa_circ_358024,RMVar_hsa_circ_301402,RMVar_hsa_circ_121793,RMVar_hsa_circ_112038,RMVar_hsa_circ_216830,RMVar_hsa_circ_24946,RMVar_hsa_circ_216832,RMVar_hsa_circ_216833,RMVar_hsa_circ_216831,RMVar_hsa_circ_104839,RMVar_hsa_circ_285869,RMVar_hsa_circ_295885,RMVar_hsa_circ_24156,RMVar_hsa_circ_216838,RMVar_hsa_circ_216837,RMVar_hsa_circ_125096,RMVar_hsa_circ_216847,RMVar_hsa_circ_216849,RMVar_hsa_circ_357907,RMVar_hsa_circ_216848,RMVar_hsa_circ_278587,RMVar_hsa_circ_288237,RMVar_hsa_circ_313351,RMVar_hsa_circ_273655,RMVar_hsa_circ_216858,RMVar_hsa_circ_216859,RMVar_hsa_circ_216860,RMVar_hsa_circ_216857,RMVar_hsa_circ_115061,RMVar_hsa_circ_26272,RMVar_hsa_circ_322781,RMVar_hsa_circ_314740,RMVar_hsa_circ_351751,RMVar_hsa_circ_216861,RMVar_hsa_circ_348274,RMVar_hsa_circ_216862 43662 RMVar_ID_43662 Human_SNP_ID_128618445 A-to-I Human chr3 - 33637490 33637490 33637490 TTGCTCTCTTGCTAAGGCTAGAGTGCAGAGGCATGATCTCGGCTCACTGCAACCTGCACCTCCCA TTGCTCTCTTGCTAAGGCTAGAGTGCAGAGGCTTGATCTCGGCTCACTGCAACCTGCACCTCCCA T A CLASP2 Ensembl:ENSG00000163539 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs937294572 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120430,RMVar_hsa_circ_216775,RMVar_hsa_circ_54597,RMVar_hsa_circ_17296,RMVar_hsa_circ_887,RMVar_hsa_circ_670,RMVar_hsa_circ_216807,RMVar_hsa_circ_85253,RMVar_hsa_circ_216813,RMVar_hsa_circ_378220,RMVar_hsa_circ_216816,RMVar_hsa_circ_216815,RMVar_hsa_circ_57250,RMVar_hsa_circ_281120,RMVar_hsa_circ_89016,RMVar_hsa_circ_216825,RMVar_hsa_circ_375783,RMVar_hsa_circ_216827,RMVar_hsa_circ_216829,RMVar_hsa_circ_93377,RMVar_hsa_circ_216828,RMVar_hsa_circ_358024,RMVar_hsa_circ_301402,RMVar_hsa_circ_121793,RMVar_hsa_circ_112038,RMVar_hsa_circ_216830,RMVar_hsa_circ_24946,RMVar_hsa_circ_216832,RMVar_hsa_circ_216833,RMVar_hsa_circ_216831,RMVar_hsa_circ_104839,RMVar_hsa_circ_285869,RMVar_hsa_circ_295885,RMVar_hsa_circ_24156,RMVar_hsa_circ_216838,RMVar_hsa_circ_216837,RMVar_hsa_circ_125096,RMVar_hsa_circ_216847,RMVar_hsa_circ_216849,RMVar_hsa_circ_357907,RMVar_hsa_circ_216848,RMVar_hsa_circ_278587,RMVar_hsa_circ_288237,RMVar_hsa_circ_313351,RMVar_hsa_circ_273655,RMVar_hsa_circ_216858,RMVar_hsa_circ_216859,RMVar_hsa_circ_216860,RMVar_hsa_circ_216857,RMVar_hsa_circ_115061,RMVar_hsa_circ_26272,RMVar_hsa_circ_322781,RMVar_hsa_circ_314740,RMVar_hsa_circ_351751,RMVar_hsa_circ_216861,RMVar_hsa_circ_348274,RMVar_hsa_circ_216862 43663 RMVar_ID_43663 Human_SNP_ID_128621796 A-to-I Human chr3 - 33651940 33651940 33651940 AAAAGTGAAGTGGAGGCCAGGTGTGGTGGCTCATGCCTGTAATCCCTGCACTTTGGGAGGCCAAG AAAAGTGAAGTGGAGGCCAGGTGTGGTGGCTCGTGCCTGTAATCCCTGCACTTTGGGAGGCCAAG T C CLASP2 Ensembl:ENSG00000163539 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1476834570 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120430,RMVar_hsa_circ_216775,RMVar_hsa_circ_85253,RMVar_hsa_circ_216813,RMVar_hsa_circ_57250,RMVar_hsa_circ_89016,RMVar_hsa_circ_216829,RMVar_hsa_circ_93377,RMVar_hsa_circ_358024,RMVar_hsa_circ_121793,RMVar_hsa_circ_216830,RMVar_hsa_circ_24946,RMVar_hsa_circ_216831,RMVar_hsa_circ_104839,RMVar_hsa_circ_295885,RMVar_hsa_circ_24156,RMVar_hsa_circ_216837,RMVar_hsa_circ_125096,RMVar_hsa_circ_357907,RMVar_hsa_circ_216848,RMVar_hsa_circ_288237,RMVar_hsa_circ_313351,RMVar_hsa_circ_39759,RMVar_hsa_circ_216859,RMVar_hsa_circ_216860,RMVar_hsa_circ_115061,RMVar_hsa_circ_26272,RMVar_hsa_circ_314740,RMVar_hsa_circ_351751,RMVar_hsa_circ_216861,RMVar_hsa_circ_348274,RMVar_hsa_circ_216862,RMVar_hsa_circ_326065,RMVar_hsa_circ_335622,RMVar_hsa_circ_216864 43664 RMVar_ID_43664 Human_SNP_ID_128635424 A-to-I Human chr3 - 33706843 33706843 33706843 CTCTTATGTCAGCCTCCCAACTAGCTGGGACTACAGGCGCACACCACCATGCCCAACTAACTTTA CTCTTATGTCAGCCTCCCAACTAGCTGGGACTGCAGGCGCACACCACCATGCCCAACTAACTTTA T C CLASP2 Ensembl:ENSG00000163539 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs944807362 Functional Loss SNV dbSNP153 33..33 33 - - - 43665 RMVar_ID_43665 Human_SNP_ID_128660892 A-to-I Human chr3 + 33805101 33805100 33805101 TTTTCCGGCCGGGTGTGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGTGG TTTTCCGGCCGGGTGTGGTGGCTCATGCCTGT_ATCCCAGCACTTTGGGAGGCTGAGGCGGGTGG TA T PDCD6IP Ensembl:ENSG00000170248 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1287009005 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_88646,RMVar_hsa_circ_216873 43666 RMVar_ID_43666 Human_SNP_ID_128664917 A-to-I Human chr3 + 33821230 33821230 33821230 TGGGGTCTTGCTGTGTTGCTCAGGCTGACCTCAAACTCTTGGCTTCAAGAGATCCTCCTGCCTCA TGGGGTCTTGCTGTGTTGCTCAGGCTGACCTCCAACTCTTGGCTTCAAGAGATCCTCCTGCCTCA A C PDCD6IP Ensembl:ENSG00000170248 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1224960970 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88646,RMVar_hsa_circ_216874,RMVar_hsa_circ_272386,RMVar_hsa_circ_330290,RMVar_hsa_circ_356027,RMVar_hsa_circ_216873,RMVar_hsa_circ_359227,RMVar_hsa_circ_318086,RMVar_hsa_circ_47785,RMVar_hsa_circ_59454,RMVar_hsa_circ_216876,RMVar_hsa_circ_216875,RMVar_hsa_circ_216878,RMVar_hsa_circ_216879,RMVar_hsa_circ_287462 43667 RMVar_ID_43667 Human_SNP_ID_128668707 A-to-I Human chr3 + 33837046 33837046 33837046 GGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCGCCTGCCACCTCG GGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCCAGTAGCTGGGACTACAGGCGCCTGCCACCTCG A C PDCD6IP Ensembl:ENSG00000170248 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs912687689 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88646,RMVar_hsa_circ_216874,RMVar_hsa_circ_330290,RMVar_hsa_circ_356027,RMVar_hsa_circ_216873,RMVar_hsa_circ_359227,RMVar_hsa_circ_47785,RMVar_hsa_circ_335715,RMVar_hsa_circ_112002,RMVar_hsa_circ_81941,RMVar_hsa_circ_216881,RMVar_hsa_circ_13383,RMVar_hsa_circ_60710,RMVar_hsa_circ_216883,RMVar_hsa_circ_216884,RMVar_hsa_circ_216882,RMVar_hsa_circ_65962,RMVar_hsa_circ_13527,RMVar_hsa_circ_68908,RMVar_hsa_circ_103460,RMVar_hsa_circ_50804,RMVar_hsa_circ_216886,RMVar_hsa_circ_124918,RMVar_hsa_circ_216888,RMVar_hsa_circ_91726,RMVar_hsa_circ_302458,RMVar_hsa_circ_365351,RMVar_hsa_circ_216887,RMVar_hsa_circ_325905,RMVar_hsa_circ_296822,RMVar_hsa_circ_216890,RMVar_hsa_circ_216891,RMVar_hsa_circ_216889 43668 RMVar_ID_43668 Human_SNP_ID_128668708 A-to-I Human chr3 + 33837046 33837046 33837046 GGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCGCCTGCCACCTCG GGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCTGCCACCTCG A G PDCD6IP Ensembl:ENSG00000170248 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs912687689 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88646,RMVar_hsa_circ_216874,RMVar_hsa_circ_330290,RMVar_hsa_circ_356027,RMVar_hsa_circ_216873,RMVar_hsa_circ_359227,RMVar_hsa_circ_47785,RMVar_hsa_circ_335715,RMVar_hsa_circ_112002,RMVar_hsa_circ_81941,RMVar_hsa_circ_216881,RMVar_hsa_circ_13383,RMVar_hsa_circ_60710,RMVar_hsa_circ_216883,RMVar_hsa_circ_216884,RMVar_hsa_circ_216882,RMVar_hsa_circ_65962,RMVar_hsa_circ_13527,RMVar_hsa_circ_68908,RMVar_hsa_circ_103460,RMVar_hsa_circ_50804,RMVar_hsa_circ_216886,RMVar_hsa_circ_124918,RMVar_hsa_circ_216888,RMVar_hsa_circ_91726,RMVar_hsa_circ_302458,RMVar_hsa_circ_365351,RMVar_hsa_circ_216887,RMVar_hsa_circ_325905,RMVar_hsa_circ_296822,RMVar_hsa_circ_216890,RMVar_hsa_circ_216891,RMVar_hsa_circ_216889 43669 RMVar_ID_43669 Human_SNP_ID_129157292 A-to-I Human chr3 + 35746852 35746852 35746852 TCTGTCAGTTACTACATCTTTCCTAAGACTTAAAACTCTACACAGTGAATTTTTGTAAAGTGAAC TCTGTCAGTTACTACATCTTTCCTAAGACTTAGAACTCTACACAGTGAATTTTTGTAAAGTGAAC A G ARPP21 Ensembl:ENSG00000172995 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs186225158 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5072 43670 RMVar_ID_43670 Human_SNP_ID_129157301 A-to-I Human chr3 + 35746876 35746876 35746876 AAGACTTAAAACTCTACACAGTGAATTTTTGTAAAGTGAACTGGACACTATACTGTTGATTAAAT AAGACTTAAAACTCTACACAGTGAATTTTTGTGAAGTGAACTGGACACTATACTGTTGATTAAAT A G ARPP21 Ensembl:ENSG00000172995 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1331184716 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5072 43671 RMVar_ID_43671 Human_SNP_ID_129157307 A-to-I Human chr3 + 35746890 35746890 35746890 TACACAGTGAATTTTTGTAAAGTGAACTGGACACTATACTGTTGATTAAATAGGACACCTGAGTT TACACAGTGAATTTTTGTAAAGTGAACTGGACGCTATACTGTTGATTAAATAGGACACCTGAGTT A G ARPP21 Ensembl:ENSG00000172995 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1376716317 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5072 43672 RMVar_ID_43672 Human_SNP_ID_129157308 A-to-I Human chr3 + 35746893 35746893 35746893 ACAGTGAATTTTTGTAAAGTGAACTGGACACTATACTGTTGATTAAATAGGACACCTGAGTTCCC ACAGTGAATTTTTGTAAAGTGAACTGGACACTGTACTGTTGATTAAATAGGACACCTGAGTTCCC A G ARPP21 Ensembl:ENSG00000172995 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs948445079 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5072 43673 RMVar_ID_43673 Human_SNP_ID_129466167 A-to-I Human chr3 + 36999935 36999935 36999935 ACCACCATGCCTATTTTTGTTTTTGTAGAAATAGGGCCTTGCTTTGTTGCCAAGGCTGGTCTTGA ACCACCATGCCTATTTTTGTTTTTGTAGAAATCGGGCCTTGCTTTGTTGCCAAGGCTGGTCTTGA A C MLH1 Ensembl:ENSG00000076242 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1449964910 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_299501,RMVar_hsa_circ_337237,RMVar_hsa_circ_308632,RMVar_hsa_circ_72634,RMVar_hsa_circ_269899,RMVar_hsa_circ_16336,RMVar_hsa_circ_17073,RMVar_hsa_circ_216964,RMVar_hsa_circ_216966,RMVar_hsa_circ_216967,RMVar_hsa_circ_216965,RMVar_hsa_circ_315485,RMVar_hsa_circ_336591,RMVar_hsa_circ_366720,RMVar_hsa_circ_71045,RMVar_hsa_circ_216968 43674 RMVar_ID_43674 Human_SNP_ID_129471085 A-to-I Human chr3 - 37016857 37016857 37016857 GGGGGTGGACCCCAAGTTCCTGAGGAACATGCACTTTGCCAAGAAGCACAACAAGAAGGGCCTAA GGGGGTGGACCCCAAGTTCCTGAGGAACATGCGCTTTGCCAAGAAGCACAACAAGAAGGGCCTAA T C RPL29P11 Ensembl:ENSG00000224858 Pseudogene exon GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs547084555 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1817777,Human_miRNA_ID_1817898,Human_miRNA_ID_1832476,Human_miRNA_ID_1833868,Human_miRNA_ID_1839581,Human_miRNA_ID_1839703,Human_miRNA_ID_1842785,Human_miRNA_ID_1888624,Human_miRNA_ID_1888782,Human_miRNA_ID_1888940,Human_miRNA_ID_1889110,Human_miRNA_ID_1891127,Human_miRNA_ID_1891348,Human_miRNA_ID_1892297,Human_miRNA_ID_1911781 43675 RMVar_ID_43675 Human_SNP_ID_129474870 A-to-I Human chr3 + 37029860 37029844 37029861 TTTTTTTTTTTTTTTTTTTGACACAGGGTCTCACTTTGTCACCCAGCTGGAGTGTGGTGGTGCAA TTTTTTTTTTTTTTTTT_________________TTTGTCACCCAGCTGGAGTGTGGTGGTGCAA TTTGACACAGGGTCTCAC T MLH1 Ensembl:ENSG00000076242 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1380186228 Functional Loss DEL dbSNP153 18..34 33 - - - RMVar_hsa_circ_4486,RMVar_hsa_circ_4958,RMVar_hsa_circ_17073,RMVar_hsa_circ_216967,RMVar_hsa_circ_19777,RMVar_hsa_circ_350633,RMVar_hsa_circ_34122,RMVar_hsa_circ_23418,RMVar_hsa_circ_27452 43676 RMVar_ID_43676 Human_SNP_ID_129474913 A-to-I Human chr3 + 37030026 37030026 37030026 AATTTTTCTTTTCTTAGAGGTGGGGTTTTGCCATGTTTCCCAGGCTGGTCTTGAACTCCTAGGCT AATTTTTCTTTTCTTAGAGGTGGGGTTTTGCCGTGTTTCCCAGGCTGGTCTTGAACTCCTAGGCT A G MLH1 Ensembl:ENSG00000076242 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs750936247 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4486,RMVar_hsa_circ_4958,RMVar_hsa_circ_17073,RMVar_hsa_circ_216967,RMVar_hsa_circ_19777,RMVar_hsa_circ_350633,RMVar_hsa_circ_34122,RMVar_hsa_circ_23418,RMVar_hsa_circ_27452 43677 RMVar_ID_43677 Human_SNP_ID_129474914 A-to-I Human chr3 + 37030026 37030026 37030026 AATTTTTCTTTTCTTAGAGGTGGGGTTTTGCCATGTTTCCCAGGCTGGTCTTGAACTCCTAGGCT AATTTTTCTTTTCTTAGAGGTGGGGTTTTGCCTTGTTTCCCAGGCTGGTCTTGAACTCCTAGGCT A T MLH1 Ensembl:ENSG00000076242 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs750936247 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4486,RMVar_hsa_circ_4958,RMVar_hsa_circ_17073,RMVar_hsa_circ_216967,RMVar_hsa_circ_19777,RMVar_hsa_circ_350633,RMVar_hsa_circ_34122,RMVar_hsa_circ_23418,RMVar_hsa_circ_27452 43678 RMVar_ID_43678 Human_SNP_ID_129477718 A-to-I Human chr3 + 37042605 37042594 37042606 ATACTCGGCCGGGTGCGGTGGCTCATGCCTGTAATCCCACCACTTTGGGAGGCTGAGGCGGGCAG ATACTCGGCCGGGTGCGGTGGC____________TCCCACCACTTTGGGAGGCTGAGGCGGGCAG CTCATGCCTGTAA C MLH1 Ensembl:ENSG00000076242 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1346662662 Functional Loss DEL dbSNP153 23..34 33 - - - RMVar_hsa_circ_17073,RMVar_hsa_circ_19777,RMVar_hsa_circ_350633,RMVar_hsa_circ_34122,RMVar_hsa_circ_21319,RMVar_hsa_circ_338650 43679 RMVar_ID_43679 Human_SNP_ID_129477746 A-to-I Human chr3 + 37042739 37042729 37042739 AATATTAGCAGGGTATGGTGGTGGGCGCCTGTAATCCCAGCTACTCAGGAGGCTAAGGCAGGAGA AATATTAGCAGGGTATGGTGGTG__________ATCCCAGCTACTCAGGAGGCTAAGGCAGGAGA GGGCGCCTGTA G MLH1 Ensembl:ENSG00000076242 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1373051253 Functional Loss DEL dbSNP153 24..33 33 - - - RMVar_hsa_circ_17073,RMVar_hsa_circ_19777,RMVar_hsa_circ_350633,RMVar_hsa_circ_34122,RMVar_hsa_circ_21319,RMVar_hsa_circ_338650 43680 RMVar_ID_43680 Human_SNP_ID_129478083 A-to-I Human chr3 + 37044140 37044140 37044140 TCGGCTTACTGCAACCTCCACCTCCTGGGTTCAGGCAATTCTCCTGCCTCAGCCTCCTGAGTAGC TCGGCTTACTGCAACCTCCACCTCCTGGGTTCGGGCAATTCTCCTGCCTCAGCCTCCTGAGTAGC A G MLH1 Ensembl:ENSG00000076242 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1409074601 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17073,RMVar_hsa_circ_19777,RMVar_hsa_circ_350633,RMVar_hsa_circ_34122,RMVar_hsa_circ_21319,RMVar_hsa_circ_338650 43681 RMVar_ID_43681 Human_SNP_ID_129478732 A-to-I Human chr3 + 37046746 37046746 37046746 CTCCTGCCTCAGCCTCCCGAATAGCTGGGACTACAGGCGCCCACCACCACGCCCAGCTAATTTTT CTCCTGCCTCAGCCTCCCGAATAGCTGGGACTGCAGGCGCCCACCACCACGCCCAGCTAATTTTT A G MLH1 Ensembl:ENSG00000076242 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1249177242 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17073,RMVar_hsa_circ_19777,RMVar_hsa_circ_350633,RMVar_hsa_circ_34122,RMVar_hsa_circ_21319,RMVar_hsa_circ_338650 43682 RMVar_ID_43682 Human_SNP_ID_129478754 A-to-I Human chr3 + 37046813 37046813 37046813 TATTTTTAGTAGAGACAGGGTTTCACCATGTTAGCAAGGATGGTCTCGATCTGACCTCGTGATCC TATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCAAGGATGGTCTCGATCTGACCTCGTGATCC A G MLH1 Ensembl:ENSG00000076242 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1156545425 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17073,RMVar_hsa_circ_19777,RMVar_hsa_circ_350633,RMVar_hsa_circ_34122,RMVar_hsa_circ_21319,RMVar_hsa_circ_338650 43683 RMVar_ID_43683 Human_SNP_ID_129481437 A-to-I Human chr3 - 37055394 37055394 37055394 GCCCAGCTAATTTTTATATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGATGGTCGCCT GCCCAGCTAATTTTTATATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGATGGTCGCCT T C LRRFIP2 Ensembl:ENSG00000093167 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1435969630 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55097,RMVar_hsa_circ_335426 43684 RMVar_ID_43684 Human_SNP_ID_129481439 A-to-I Human chr3 - 37055400 37055400 37055400 CACCACGCCCAGCTAATTTTTATATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGATGG CACCACGCCCAGCTAATTTTTATATTTTTAGTTGAGACAGGGTTTCACCATGTTGGCCAGGATGG T A LRRFIP2 Ensembl:ENSG00000093167 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs983880577 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55097,RMVar_hsa_circ_335426 43685 RMVar_ID_43685 Human_SNP_ID_129481443 A-to-I Human chr3 - 37055411 37055411 37055411 CAGGCCTGTGCCACCACGCCCAGCTAATTTTTATATTTTTAGTAGAGACAGGGTTTCACCATGTT CAGGCCTGTGCCACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTT T C LRRFIP2 Ensembl:ENSG00000093167 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1354197428 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55097,RMVar_hsa_circ_335426 43686 RMVar_ID_43686 Human_SNP_ID_129482014 A-to-I Human chr3 - 37057646 37057646 37057646 AAGACATGTTGGGGCCAGGCGTGGTGGCCCGCACCCATAATCCCAGCATTTGGAGAGGCTGAGGT AAGACATGTTGGGGCCAGGCGTGGTGGCCCGCGCCCATAATCCCAGCATTTGGAGAGGCTGAGGT T C LRRFIP2 Ensembl:ENSG00000093167 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs770499648 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55097,RMVar_hsa_circ_335426 43687 RMVar_ID_43687 Human_SNP_ID_129485231 A-to-I Human chr3 - 37071914 37071914 37071914 TCTTCATTGCTGTTTTGCTAAGCCTTGCAGGTAGATTCCATGTACACCAAAAGCTGGAAAAAATT TCTTCATTGCTGTTTTGCTAAGCCTTGCAGGTGGATTCCATGTACACCAAAAGCTGGAAAAAATT T C LRRFIP2 Ensembl:ENSG00000093167 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs17810211 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28392,RMVar_hsa_circ_216982,RMVar_hsa_circ_307497,RMVar_hsa_circ_366508,RMVar_hsa_circ_368143,RMVar_hsa_circ_321277,RMVar_hsa_circ_72192,RMVar_hsa_circ_319873,RMVar_hsa_circ_70467,RMVar_hsa_circ_38058,RMVar_hsa_circ_115564,RMVar_hsa_circ_216983,RMVar_hsa_circ_216984 43688 RMVar_ID_43688 Human_SNP_ID_129485752 A-to-I Human chr3 - 37074167 37074167 37074167 CTCTCCCTCTTTCTCTCTTTCCCCTCGGACCTACCTCTTAATATGTCTCTCTACAAATGATTTTT CTCTCCCTCTTTCTCTCTTTCCCCTCGGACCTGCCTCTTAATATGTCTCTCTACAAATGATTTTT T C LRRFIP2 Ensembl:ENSG00000093167 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1558527 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5003,GWAS_ID_5004,GWAS_ID_5005,GWAS_ID_5006,GWAS_ID_5007,GWAS_ID_5008,GWAS_ID_5009,GWAS_ID_5010 RMVar_hsa_circ_28717,RMVar_hsa_circ_28392,RMVar_hsa_circ_216982,RMVar_hsa_circ_307497,RMVar_hsa_circ_366508,RMVar_hsa_circ_368143,RMVar_hsa_circ_321277,RMVar_hsa_circ_72192,RMVar_hsa_circ_319873,RMVar_hsa_circ_70467,RMVar_hsa_circ_38058,RMVar_hsa_circ_115564,RMVar_hsa_circ_216983,RMVar_hsa_circ_38934,RMVar_hsa_circ_216984,RMVar_hsa_circ_216985,RMVar_hsa_circ_4496 43689 RMVar_ID_43689 Human_SNP_ID_129491503 A-to-I Human chr3 - 37100216 37100216 37100216 GGCTCAACTGATCTTCCTGCCTCAGTCTCTCAAAGCGCTGGGATTACAGGTGATTTGTGTATTTT GGCTCAACTGATCTTCCTGCCTCAGTCTCTCAGAGCGCTGGGATTACAGGTGATTTGTGTATTTT T C LRRFIP2 Ensembl:ENSG00000093167 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs573808320 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28392,RMVar_hsa_circ_368143,RMVar_hsa_circ_70467,RMVar_hsa_circ_38058,RMVar_hsa_circ_115564,RMVar_hsa_circ_216984,RMVar_hsa_circ_55831,RMVar_hsa_circ_43587,RMVar_hsa_circ_4496,RMVar_hsa_circ_355949,RMVar_hsa_circ_356093,RMVar_hsa_circ_48713,RMVar_hsa_circ_346911,RMVar_hsa_circ_358329,RMVar_hsa_circ_24351,RMVar_hsa_circ_353627,RMVar_hsa_circ_45358,RMVar_hsa_circ_98311,RMVar_hsa_circ_44411,RMVar_hsa_circ_22117,RMVar_hsa_circ_73345,RMVar_hsa_circ_350516,RMVar_hsa_circ_216990,RMVar_hsa_circ_360745,RMVar_hsa_circ_27906 43690 RMVar_ID_43690 Human_SNP_ID_129491831 A-to-I Human chr3 - 37101275 37101275 37101275 TTGGCTTACTGCAACCCCCACCCTCCGAGTTCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGC TTGGCTTACTGCAACCCCCACCCTCCGAGTTCGAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGC T C LRRFIP2 Ensembl:ENSG00000093167 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1390389626 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14801065 RMVar_hsa_circ_28392,RMVar_hsa_circ_368143,RMVar_hsa_circ_70467,RMVar_hsa_circ_38058,RMVar_hsa_circ_115564,RMVar_hsa_circ_216984,RMVar_hsa_circ_55831,RMVar_hsa_circ_43587,RMVar_hsa_circ_4496,RMVar_hsa_circ_355949,RMVar_hsa_circ_356093,RMVar_hsa_circ_48713,RMVar_hsa_circ_346911,RMVar_hsa_circ_358329,RMVar_hsa_circ_24351,RMVar_hsa_circ_353627,RMVar_hsa_circ_45358,RMVar_hsa_circ_98311,RMVar_hsa_circ_44411,RMVar_hsa_circ_22117,RMVar_hsa_circ_73345,RMVar_hsa_circ_350516,RMVar_hsa_circ_216990,RMVar_hsa_circ_360745,RMVar_hsa_circ_27906 43691 RMVar_ID_43691 Human_SNP_ID_129493270 A-to-I Human chr3 - 37107173 37107159 37107174 TTCCTGTCCGGGCATGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGGCACATTA TTCCTGTCCGGGCATGGTGGCTCACGCCTGT_______________GGAGGCCGAGGGCACATTA CCAAAGTGCTGGGATT C LRRFIP2 Ensembl:ENSG00000093167 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs572315024 Functional Loss DEL dbSNP153 32..46 33 - - - RMVar_hsa_circ_5353,RMVar_hsa_circ_28392,RMVar_hsa_circ_368143,RMVar_hsa_circ_70467,RMVar_hsa_circ_38058,RMVar_hsa_circ_115564,RMVar_hsa_circ_216984,RMVar_hsa_circ_55831,RMVar_hsa_circ_43587,RMVar_hsa_circ_355949,RMVar_hsa_circ_356093,RMVar_hsa_circ_48713,RMVar_hsa_circ_346911,RMVar_hsa_circ_358329,RMVar_hsa_circ_24351,RMVar_hsa_circ_353627,RMVar_hsa_circ_45358,RMVar_hsa_circ_98311,RMVar_hsa_circ_44411,RMVar_hsa_circ_22117,RMVar_hsa_circ_73345,RMVar_hsa_circ_350516,RMVar_hsa_circ_216990,RMVar_hsa_circ_360745,RMVar_hsa_circ_27906,RMVar_hsa_circ_33463,RMVar_hsa_circ_339684,RMVar_hsa_circ_42853,RMVar_hsa_circ_323905,RMVar_hsa_circ_341258,RMVar_hsa_circ_47571 43692 RMVar_ID_43692 Human_SNP_ID_129504409 A-to-I Human chr3 - 37155935 37155935 37155935 GGGAGGCCGAGGTTGCAGTGAGCCAAGGTCGCACTATTGCACTCCAGCCTGGGAGACAGAGTGGG GGGAGGCCGAGGTTGCAGTGAGCCAAGGTCGCGCTATTGCACTCCAGCCTGGGAGACAGAGTGGG T C LRRFIP2 Ensembl:ENSG00000093167 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1281268696 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_313473 43693 RMVar_ID_43693 Human_SNP_ID_129505972 A-to-I Human chr3 - 37161938 37161938 37161938 GCTCAAGGGATCCACCTGCCTTGGTCTCCCAAAATGTTGGGATTACAGACATGAACCACCGCACC GCTCAAGGGATCCACCTGCCTTGGTCTCCCAACATGTTGGGATTACAGACATGAACCACCGCACC T G LRRFIP2 Ensembl:ENSG00000093167 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1405668819 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_313473 43694 RMVar_ID_43694 Human_SNP_ID_129508744 A-to-I Human chr3 - 37172751 37172751 37172751 GATCATGTGTTATACTTCTTCATTAGTTCATTATTCATTTATTTTGATGGGGAGGTCAAGAGATA GATCATGTGTTATACTTCTTCATTAGTTCATTGTTCATTTATTTTGATGGGGAGGTCAAGAGATA T C LRRFIP2 Ensembl:ENSG00000093167 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs375753994 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2782409,Human_RBP_ID_3706290 RMVar_hsa_circ_313473 43695 RMVar_ID_43695 Human_SNP_ID_129529152 A-to-I Human chr3 + 37253158 37253158 37253158 GCACCTGTGTGGTCCCAGCTACTCAGGAGGCTAAGGCAGGGGCATTACTTGAGCCTCGGAGGTCG GCACCTGTGTGGTCCCAGCTACTCAGGAGGCTGAGGCAGGGGCATTACTTGAGCCTCGGAGGTCG A G GOLGA4 Ensembl:ENSG00000144674 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs960854524 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1723,RMVar_hsa_circ_61622,RMVar_hsa_circ_80428,RMVar_hsa_circ_77830,RMVar_hsa_circ_216999,RMVar_hsa_circ_301179,RMVar_hsa_circ_353326,RMVar_hsa_circ_217000,RMVar_hsa_circ_301231,RMVar_hsa_circ_62266,RMVar_hsa_circ_38378,RMVar_hsa_circ_52092 43696 RMVar_ID_43696 Human_SNP_ID_129529153 A-to-I Human chr3 + 37253158 37253158 37253158 GCACCTGTGTGGTCCCAGCTACTCAGGAGGCTAAGGCAGGGGCATTACTTGAGCCTCGGAGGTCG GCACCTGTGTGGTCCCAGCTACTCAGGAGGCTTAGGCAGGGGCATTACTTGAGCCTCGGAGGTCG A T GOLGA4 Ensembl:ENSG00000144674 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs960854524 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1723,RMVar_hsa_circ_61622,RMVar_hsa_circ_80428,RMVar_hsa_circ_77830,RMVar_hsa_circ_216999,RMVar_hsa_circ_301179,RMVar_hsa_circ_353326,RMVar_hsa_circ_217000,RMVar_hsa_circ_301231,RMVar_hsa_circ_62266,RMVar_hsa_circ_38378,RMVar_hsa_circ_52092 43697 RMVar_ID_43697 Human_SNP_ID_129530972 A-to-I Human chr3 + 37258575 37258575 37258575 GCCTGGAATGCCTGACCTCAAGTGATCTGCCCACCTTGGACTCCTAAAGTGCTGGGATTACAGGC GCCTGGAATGCCTGACCTCAAGTGATCTGCCCGCCTTGGACTCCTAAAGTGCTGGGATTACAGGC A G GOLGA4 Ensembl:ENSG00000144674 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1189167007 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1723,RMVar_hsa_circ_61622,RMVar_hsa_circ_80428,RMVar_hsa_circ_77830,RMVar_hsa_circ_216999,RMVar_hsa_circ_301179,RMVar_hsa_circ_353326,RMVar_hsa_circ_217000,RMVar_hsa_circ_301231,RMVar_hsa_circ_62266,RMVar_hsa_circ_38378,RMVar_hsa_circ_52092 43698 RMVar_ID_43698 Human_SNP_ID_129530978 A-to-I Human chr3 + 37258602 37258602 37258602 TGCCCACCTTGGACTCCTAAAGTGCTGGGATTACAGGCATGAACCACCACACCTGGCCCCAGTTG TGCCCACCTTGGACTCCTAAAGTGCTGGGATTGCAGGCATGAACCACCACACCTGGCCCCAGTTG A G GOLGA4 Ensembl:ENSG00000144674 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1341405588 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14802681 RMVar_hsa_circ_1723,RMVar_hsa_circ_61622,RMVar_hsa_circ_80428,RMVar_hsa_circ_77830,RMVar_hsa_circ_216999,RMVar_hsa_circ_301179,RMVar_hsa_circ_353326,RMVar_hsa_circ_217000,RMVar_hsa_circ_301231,RMVar_hsa_circ_62266,RMVar_hsa_circ_38378,RMVar_hsa_circ_52092 43699 RMVar_ID_43699 Human_SNP_ID_129532843 A-to-I Human chr3 + 37266341 37266341 37266341 CCTGCCTCAGCCTCCTGAGTGGCTGGGACTACAGGTGCGCACCACTATGCCTGGCTAATTTTTGT CCTGCCTCAGCCTCCTGAGTGGCTGGGACTACGGGTGCGCACCACTATGCCTGGCTAATTTTTGT A G GOLGA4 Ensembl:ENSG00000144674 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1380816472 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14802862 RMVar_hsa_circ_1723,RMVar_hsa_circ_61622,RMVar_hsa_circ_80428,RMVar_hsa_circ_77830,RMVar_hsa_circ_216999,RMVar_hsa_circ_301179,RMVar_hsa_circ_353326,RMVar_hsa_circ_217000,RMVar_hsa_circ_301231,RMVar_hsa_circ_62266,RMVar_hsa_circ_38378,RMVar_hsa_circ_52092 43700 RMVar_ID_43700 Human_SNP_ID_129533377 A-to-I Human chr3 + 37268711 37268711 37268711 CGCCCACTTCAGCCTCCCAAGTAGCTGGGACCACAGATGCGCACCACCATACCTGGCTAACTTTT CGCCCACTTCAGCCTCCCAAGTAGCTGGGACCGCAGATGCGCACCACCATACCTGGCTAACTTTT A G GOLGA4 Ensembl:ENSG00000144674 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs541296344 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1723,RMVar_hsa_circ_61622,RMVar_hsa_circ_80428,RMVar_hsa_circ_77830,RMVar_hsa_circ_216999,RMVar_hsa_circ_301179,RMVar_hsa_circ_353326,RMVar_hsa_circ_217000,RMVar_hsa_circ_301231,RMVar_hsa_circ_62266,RMVar_hsa_circ_38378,RMVar_hsa_circ_52092,RMVar_hsa_circ_217001 43701 RMVar_ID_43701 Human_SNP_ID_129533941 A-to-I Human chr3 + 37270971 37270971 37270971 CTAGATGGTCCCTTCTGAGGGTGATGGGAGACAGTGACAGATCATCAGGCATTACATTCTCATTA CTAGATGGTCCCTTCTGAGGGTGATGGGAGACGGTGACAGATCATCAGGCATTACATTCTCATTA A G GOLGA4 Ensembl:ENSG00000144674 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs962839514 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1723,RMVar_hsa_circ_61622,RMVar_hsa_circ_80428,RMVar_hsa_circ_77830,RMVar_hsa_circ_216999,RMVar_hsa_circ_301179,RMVar_hsa_circ_353326,RMVar_hsa_circ_217000,RMVar_hsa_circ_301231,RMVar_hsa_circ_62266,RMVar_hsa_circ_38378,RMVar_hsa_circ_52092,RMVar_hsa_circ_217001 43702 RMVar_ID_43702 Human_SNP_ID_129534615 A-to-I Human chr3 + 37273993 37273990 37273994 GGAGTGGCGCATGCCTGAAATCCCAGCTACTTAGTTGGCTGAAGCGTGAGAATCGCTTGAACCCA GGAGTGGCGCATGCCTGAAATCCCAGCTAC____TTGGCTGAAGCGTGAGAATCGCTTGAACCCA CTTAG C GOLGA4 Ensembl:ENSG00000144674 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs975175973 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_22605491 RMVar_hsa_circ_1723,RMVar_hsa_circ_61622,RMVar_hsa_circ_77830,RMVar_hsa_circ_216999,RMVar_hsa_circ_353326,RMVar_hsa_circ_301231,RMVar_hsa_circ_62266,RMVar_hsa_circ_38378,RMVar_hsa_circ_52092,RMVar_hsa_circ_12711,RMVar_hsa_circ_265050,RMVar_hsa_circ_278608,RMVar_hsa_circ_306619,RMVar_hsa_circ_352827,RMVar_hsa_circ_217001,RMVar_hsa_circ_321372,RMVar_hsa_circ_283510,RMVar_hsa_circ_269453,RMVar_hsa_circ_63008,RMVar_hsa_circ_75162,RMVar_hsa_circ_50216,RMVar_hsa_circ_217003,RMVar_hsa_circ_217004,RMVar_hsa_circ_217005,RMVar_hsa_circ_217002 43703 RMVar_ID_43703 Human_SNP_ID_129535241 A-to-I Human chr3 + 37276114 37276114 37276114 TCCTCGGGCACCAAGCACTTCTGATTCTGTGCAGTTGAAGTGTAGGGAGATGCTTGCTGCAGCTC TCCTCGGGCACCAAGCACTTCTGATTCTGTGCGGTTGAAGTGTAGGGAGATGCTTGCTGCAGCTC A G TCEA1P2,GOLGA4 Ensembl:ENSG00000230409,Ensembl:ENSG00000144674 Pseudogene,Protein coding exon,intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1380853105 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1205263,Human_RBP_ID_3723325,Human_RBP_ID_17195308,Human_RBP_ID_26346599,Human_RBP_ID_27823074 RMVar_hsa_circ_1723,RMVar_hsa_circ_61622,RMVar_hsa_circ_77830,RMVar_hsa_circ_216999,RMVar_hsa_circ_353326,RMVar_hsa_circ_301231,RMVar_hsa_circ_62266,RMVar_hsa_circ_38378,RMVar_hsa_circ_52092,RMVar_hsa_circ_12711,RMVar_hsa_circ_265050,RMVar_hsa_circ_278608,RMVar_hsa_circ_306619,RMVar_hsa_circ_352827,RMVar_hsa_circ_217001,RMVar_hsa_circ_321372,RMVar_hsa_circ_283510,RMVar_hsa_circ_269453,RMVar_hsa_circ_63008,RMVar_hsa_circ_75162,RMVar_hsa_circ_50216,RMVar_hsa_circ_217003,RMVar_hsa_circ_217004,RMVar_hsa_circ_217005,RMVar_hsa_circ_217002 43704 RMVar_ID_43704 Human_SNP_ID_129535726 A-to-I Human chr3 + 37278255 37278246 37278256 GAGTTTTGCTCTTTTTGCCCAGGCTGGAGCGTAATGGCGTGATCTCAGCTCACTGCAACCTCTGC GAGTTTTGCTCTTTTTGCCCAGGC__________TGGCGTGATCTCAGCTCACTGCAACCTCTGC CTGGAGCGTAA C GOLGA4 Ensembl:ENSG00000144674 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1559373860 Functional Loss DEL dbSNP153 25..34 33 - - - Human_RBP_ID_783426,Human_RBP_ID_14979230 RMVar_hsa_circ_1723,RMVar_hsa_circ_61622,RMVar_hsa_circ_77830,RMVar_hsa_circ_216999,RMVar_hsa_circ_353326,RMVar_hsa_circ_301231,RMVar_hsa_circ_62266,RMVar_hsa_circ_38378,RMVar_hsa_circ_52092,RMVar_hsa_circ_12711,RMVar_hsa_circ_265050,RMVar_hsa_circ_278608,RMVar_hsa_circ_306619,RMVar_hsa_circ_352827,RMVar_hsa_circ_217001,RMVar_hsa_circ_321372,RMVar_hsa_circ_283510,RMVar_hsa_circ_269453,RMVar_hsa_circ_63008,RMVar_hsa_circ_75162,RMVar_hsa_circ_50216,RMVar_hsa_circ_217003,RMVar_hsa_circ_217004,RMVar_hsa_circ_217005,RMVar_hsa_circ_217002 43705 RMVar_ID_43705 Human_SNP_ID_129535739 A-to-I Human chr3 + 37278293 37278293 37278293 GTGATCTCAGCTCACTGCAACCTCTGCCTCCCAGATTCAAACGATTTTCATGCCTCAGCCTCCTG GTGATCTCAGCTCACTGCAACCTCTGCCTCCCGGATTCAAACGATTTTCATGCCTCAGCCTCCTG A G GOLGA4 Ensembl:ENSG00000144674 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1235720333 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25734740 RMVar_hsa_circ_1723,RMVar_hsa_circ_61622,RMVar_hsa_circ_77830,RMVar_hsa_circ_216999,RMVar_hsa_circ_353326,RMVar_hsa_circ_301231,RMVar_hsa_circ_62266,RMVar_hsa_circ_38378,RMVar_hsa_circ_52092,RMVar_hsa_circ_12711,RMVar_hsa_circ_265050,RMVar_hsa_circ_278608,RMVar_hsa_circ_306619,RMVar_hsa_circ_352827,RMVar_hsa_circ_217001,RMVar_hsa_circ_321372,RMVar_hsa_circ_283510,RMVar_hsa_circ_269453,RMVar_hsa_circ_63008,RMVar_hsa_circ_75162,RMVar_hsa_circ_50216,RMVar_hsa_circ_217003,RMVar_hsa_circ_217004,RMVar_hsa_circ_217005,RMVar_hsa_circ_217002 43706 RMVar_ID_43706 Human_SNP_ID_129544355 A-to-I Human chr3 + 37312707 37312707 37312707 CACGGCTCCTGGCTAATTTTTAATTTTTTTGTAGAGATGGGATTTCACTGTGTTGCCTAGGCTGG CACGGCTCCTGGCTAATTTTTAATTTTTTTGTGGAGATGGGATTTCACTGTGTTGCCTAGGCTGG A G GOLGA4 Ensembl:ENSG00000144674 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1275840157 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14803622 RMVar_hsa_circ_62266,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_360894,RMVar_hsa_circ_325550,RMVar_hsa_circ_55293,RMVar_hsa_circ_53532,RMVar_hsa_circ_357716,RMVar_hsa_circ_362324,RMVar_hsa_circ_354130,RMVar_hsa_circ_357008,RMVar_hsa_circ_124805,RMVar_hsa_circ_53653,RMVar_hsa_circ_66262,RMVar_hsa_circ_217008,RMVar_hsa_circ_355264,RMVar_hsa_circ_217011,RMVar_hsa_circ_116224,RMVar_hsa_circ_217012,RMVar_hsa_circ_217014,RMVar_hsa_circ_46013,RMVar_hsa_circ_330625,RMVar_hsa_circ_354853,RMVar_hsa_circ_55758 43707 RMVar_ID_43707 Human_SNP_ID_129544766 A-to-I Human chr3 + 37314431 37314431 37314431 GGGAGGACAAGGTGGGTGGATCACTTGAGGTCAGGAGTTTGAGACCAGCCTGAACAATATGGTGA GGGAGGACAAGGTGGGTGGATCACTTGAGGTCGGGAGTTTGAGACCAGCCTGAACAATATGGTGA A G GOLGA4 Ensembl:ENSG00000144674 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1424727671 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_62266,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_360894,RMVar_hsa_circ_325550,RMVar_hsa_circ_55293,RMVar_hsa_circ_53532,RMVar_hsa_circ_357716,RMVar_hsa_circ_362324,RMVar_hsa_circ_354130,RMVar_hsa_circ_357008,RMVar_hsa_circ_124805,RMVar_hsa_circ_53653,RMVar_hsa_circ_66262,RMVar_hsa_circ_217008,RMVar_hsa_circ_355264,RMVar_hsa_circ_217011,RMVar_hsa_circ_116224,RMVar_hsa_circ_217012,RMVar_hsa_circ_217014,RMVar_hsa_circ_46013,RMVar_hsa_circ_330625,RMVar_hsa_circ_354853,RMVar_hsa_circ_55758 43708 RMVar_ID_43708 Human_SNP_ID_129544790 A-to-I Human chr3 + 37314553 37314553 37314553 GTCCCAGCTACTTGGGAGGCTGAGGCAGGAGTATTGCTTGAACCCGCGAGGCAGAGGTTGCAGTG GTCCCAGCTACTTGGGAGGCTGAGGCAGGAGTGTTGCTTGAACCCGCGAGGCAGAGGTTGCAGTG A G GOLGA4 Ensembl:ENSG00000144674 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs922462394 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_62266,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_360894,RMVar_hsa_circ_325550,RMVar_hsa_circ_55293,RMVar_hsa_circ_53532,RMVar_hsa_circ_357716,RMVar_hsa_circ_362324,RMVar_hsa_circ_354130,RMVar_hsa_circ_357008,RMVar_hsa_circ_124805,RMVar_hsa_circ_53653,RMVar_hsa_circ_66262,RMVar_hsa_circ_217008,RMVar_hsa_circ_355264,RMVar_hsa_circ_217011,RMVar_hsa_circ_116224,RMVar_hsa_circ_217012,RMVar_hsa_circ_217014,RMVar_hsa_circ_46013,RMVar_hsa_circ_330625,RMVar_hsa_circ_354853,RMVar_hsa_circ_55758 43709 RMVar_ID_43709 Human_SNP_ID_129550732 A-to-I Human chr3 + 37336660 37336660 37336660 GGGCATGGTGGCGCATGCCTGTGGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAA GGGCATGGTGGCGCATGCCTGTGGTCCCAGCTGCTTGGGAGGCTGAGGCAGGAGAATCGCTTGAA A G GOLGA4 Ensembl:ENSG00000144674 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1424576598 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38378,RMVar_hsa_circ_52092,RMVar_hsa_circ_265050,RMVar_hsa_circ_75162,RMVar_hsa_circ_55293,RMVar_hsa_circ_53532,RMVar_hsa_circ_362324,RMVar_hsa_circ_124805,RMVar_hsa_circ_66262,RMVar_hsa_circ_217008,RMVar_hsa_circ_217016,RMVar_hsa_circ_367906,RMVar_hsa_circ_67407,RMVar_hsa_circ_311403,RMVar_hsa_circ_57901,RMVar_hsa_circ_73190,RMVar_hsa_circ_367037,RMVar_hsa_circ_31843,RMVar_hsa_circ_366691,RMVar_hsa_circ_278083,RMVar_hsa_circ_281191,RMVar_hsa_circ_217017,RMVar_hsa_circ_217015 43710 RMVar_ID_43710 Human_SNP_ID_129552558 A-to-I Human chr3 + 37343382 37343382 37343382 ACCTCGGGTGATCCGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGACGTGAGCCACCGTGC ACCTCGGGTGATCCGCCTGCCTCGGCCTCCCACAGTGCTGGGATTACAGACGTGAGCCACCGTGC A C GOLGA4 Ensembl:ENSG00000144674 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs369257486 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38378,RMVar_hsa_circ_75162,RMVar_hsa_circ_55293,RMVar_hsa_circ_66262,RMVar_hsa_circ_217016,RMVar_hsa_circ_367906,RMVar_hsa_circ_311403,RMVar_hsa_circ_57901,RMVar_hsa_circ_31843,RMVar_hsa_circ_281191,RMVar_hsa_circ_217017,RMVar_hsa_circ_217018,RMVar_hsa_circ_364489 43711 RMVar_ID_43711 Human_SNP_ID_129552559 A-to-I Human chr3 + 37343382 37343382 37343382 ACCTCGGGTGATCCGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGACGTGAGCCACCGTGC ACCTCGGGTGATCCGCCTGCCTCGGCCTCCCAGAGTGCTGGGATTACAGACGTGAGCCACCGTGC A G GOLGA4 Ensembl:ENSG00000144674 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs369257486 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38378,RMVar_hsa_circ_75162,RMVar_hsa_circ_55293,RMVar_hsa_circ_66262,RMVar_hsa_circ_217016,RMVar_hsa_circ_367906,RMVar_hsa_circ_311403,RMVar_hsa_circ_57901,RMVar_hsa_circ_31843,RMVar_hsa_circ_281191,RMVar_hsa_circ_217017,RMVar_hsa_circ_217018,RMVar_hsa_circ_364489 43712 RMVar_ID_43712 Human_SNP_ID_129559150 A-to-I Human chr3 + 37370188 37370188 37370188 CTTGTAATCCCAGCAATTTGGGAGGCTGAGGCAAGAGGATTGCATGAACTTGGGAGGCGGAGGTT CTTGTAATCCCAGCAATTTGGGAGGCTGAGGCGAGAGGATTGCATGAACTTGGGAGGCGGAGGTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1419055773 Functional Loss SNV dbSNP153 33..33 33 - - - 43713 RMVar_ID_43713 Human_SNP_ID_129559285 A-to-I Human chr3 + 37370635 37370635 37370635 GGGACTGCAGGCGCCTGCCGCCACGCCCGGCTAATTTTTGTATTTTTAGTAGAGACAAGGTTTCA GGGACTGCAGGCGCCTGCCGCCACGCCCGGCTGATTTTTGTATTTTTAGTAGAGACAAGGTTTCA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs902918423 Functional Loss SNV dbSNP153 33..33 33 - - - 43714 RMVar_ID_43714 Human_SNP_ID_129693469 A-to-I Human chr3 + 37952621 37952621 37952621 AGTGCCTGGCAGATTTCTTTTACTTACTGCCAAAATCATTTCTATCTGATGACAGGTATATTCTT AGTGCCTGGCAGATTTCTTTTACTTACTGCCAGAATCATTTCTATCTGATGACAGGTATATTCTT A G CTDSPL Ensembl:ENSG00000144677 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1425992162 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97253,RMVar_hsa_circ_105741,RMVar_hsa_circ_217041,RMVar_hsa_circ_217040,RMVar_hsa_circ_78443,RMVar_hsa_circ_217039,RMVar_hsa_circ_324117,RMVar_hsa_circ_357291,RMVar_hsa_circ_372790,RMVar_hsa_circ_315444,RMVar_hsa_circ_217043,RMVar_hsa_circ_12998,RMVar_hsa_circ_217044,RMVar_hsa_circ_217042 43715 RMVar_ID_43715 Human_SNP_ID_129741454 A-to-I Human chr3 - 38135026 38135026 38135026 TATTGCTGCCAGCATATTTCGCTTCCAGCCACAGGGCGGTTTTCTCCTATCTCAGTAAATAGAAC TATTGCTGCCAGCATATTTCGCTTCCAGCCACGGGGCGGTTTTCTCCTATCTCAGTAAATAGAAC T C ACAA1 Ensembl:ENSG00000060971 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs190580697 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17574271,Human_RBP_ID_22726112 RMVar_hsa_circ_217061,RMVar_hsa_circ_108622 43716 RMVar_ID_43716 Human_SNP_ID_129741480 A-to-I Human chr3 - 38135158 38135158 38135158 AAAACATGTGAGTAAAGGAATCTGCATCATAAATAAGTTCAAGGGAAGGTACTGTGCTGAGATGT AAAACATGTGAGTAAAGGAATCTGCATCATAACTAAGTTCAAGGGAAGGTACTGTGCTGAGATGT T G ACAA1 Ensembl:ENSG00000060971 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs762241663 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_217061,RMVar_hsa_circ_108622 43717 RMVar_ID_43717 Human_SNP_ID_129741542 A-to-I Human chr3 - 38135427 38135425 38135428 ATATAATGCCACATCCCTCTTGCCAAGATAGTAGAGATAGTGATCAATAAATACTGAGGGAACTC ATATAATGCCACATCCCTCTTGCCAAGATAG___AGATAGTGATCAATAAATACTGAGGGAACTC TCTA T ACAA1 Ensembl:ENSG00000060971 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs990719862 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_5133192 RMVar_hsa_circ_217061,RMVar_hsa_circ_108622 43718 RMVar_ID_43718 Human_SNP_ID_129742083 A-to-I Human chr3 - 38137051 38137051 38137051 GCGGTCAGTTCCCGGACTGGTGGCTGGTCTGCAGGGTTGACCTGCGCAATGCAGAGGCTGCAGGT GCGGTCAGTTCCCGGACTGGTGGCTGGTCTGCGGGGTTGACCTGCGCAATGCAGAGGCTGCAGGT T C ACAA1 Ensembl:ENSG00000060971 Protein coding 5'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1187204712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_834622,Human_RBP_ID_4756386,Human_RBP_ID_5391420,Human_RBP_ID_18423942,Human_RBP_ID_22455776,Human_RBP_ID_26762953 RMVar_hsa_circ_89235,RMVar_hsa_circ_217063 43719 RMVar_ID_43719 Human_SNP_ID_129794671 A-to-I Human chr3 + 38351121 38351121 38351121 TTGAACTGTGGAGAGGGAGGTTTCGGTGAGCCAAGATCGCGCCACTGCACTCCAGCCTGGACAAC TTGAACTGTGGAGAGGGAGGTTTCGGTGAGCCGAGATCGCGCCACTGCACTCCAGCCTGGACAAC A G XYLB Ensembl:ENSG00000093217 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1281499979 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59643,RMVar_hsa_circ_72756 43720 RMVar_ID_43720 Human_SNP_ID_129804371 A-to-I Human chr3 + 38391060 38391060 38391060 TGGCCAACATGGTGAAACCCCGTCTCTACTGAAAACACAAAATTAGCCAGGCATGGTGGCGGACG TGGCCAACATGGTGAAACCCCGTCTCTACTGACAACACAAAATTAGCCAGGCATGGTGGCGGACG A C XYLB Ensembl:ENSG00000093217 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1244242052 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72756,RMVar_hsa_circ_89431,RMVar_hsa_circ_49678,RMVar_hsa_circ_52250,RMVar_hsa_circ_217088,RMVar_hsa_circ_289606,RMVar_hsa_circ_11112,RMVar_hsa_circ_49504,RMVar_hsa_circ_377705,RMVar_hsa_circ_357808,RMVar_hsa_circ_332733,RMVar_hsa_circ_42637,RMVar_hsa_circ_312295,RMVar_hsa_circ_301890,RMVar_hsa_circ_360977 43721 RMVar_ID_43721 Human_SNP_ID_129810645 A-to-I Human chr3 + 38415714 38415714 38415714 CTGAGGCACGAGAATTGCTTGAACCCGGGGGCAGAGATTGCAGTGAGCCGAGATTGTGCCACTTC CTGAGGCACGAGAATTGCTTGAACCCGGGGGCGGAGATTGCAGTGAGCCGAGATTGTGCCACTTC A G XYLB Ensembl:ENSG00000093217 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1372499020 Functional Loss SNV dbSNP153 33..33 33 - - - 43722 RMVar_ID_43722 Human_SNP_ID_129810782 A-to-I Human chr3 + 38416161 38416161 38416161 GCCTAATCACATGAAATAGTATCAAACTATATATGCTTTGACAAGACAGAAGTAACAAAACAAAA GCCTAATCACATGAAATAGTATCAAACTATATGTGCTTTGACAAGACAGAAGTAACAAAACAAAA A G XYLB Ensembl:ENSG00000093217 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1016478302 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26507573 43723 RMVar_ID_43723 Human_SNP_ID_129811142 A-to-I Human chr3 + 38417610 38417610 38417610 GTTGCTCAAAAGACAGTTTCTAGCCCAGGCATAGTAGCTCATGCCTGTAATCGCAGCACTTTGAG GTTGCTCAAAAGACAGTTTCTAGCCCAGGCATGGTAGCTCATGCCTGTAATCGCAGCACTTTGAG A G XYLB Ensembl:ENSG00000093217 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1341863624 Functional Loss SNV dbSNP153 33..33 33 - - - 43724 RMVar_ID_43724 Human_SNP_ID_129811862 A-to-I Human chr3 + 38420070 38420070 38420070 TCAATCCCCCAACCTTGTGATCCACCCGCCTCAGCCTCCCAAAGTGCTGGAATTAACAGGCGTGA TCAATCCCCCAACCTTGTGATCCACCCGCCTCTGCCTCCCAAAGTGCTGGAATTAACAGGCGTGA A T XYLB Ensembl:ENSG00000093217 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs936844551 Functional Loss SNV dbSNP153 33..33 33 - - - 43725 RMVar_ID_43725 Human_SNP_ID_129819645 A-to-I Human chr3 - 38452569 38452569 38452569 GCTGGGCATGGTGACACACACCTGTAATTCCAACTACTCGGTAGGAGGCTGAGGCAGGAGAATCG GCTGGGCATGGTGACACACACCTGTAATTCCAGCTACTCGGTAGGAGGCTGAGGCAGGAGAATCG T C ACVR2B-AS1 Ensembl:ENSG00000229589 lincRNA exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs201732812 Functional Loss SNV dbSNP153 33..33 33 - - - 43726 RMVar_ID_43726 Human_SNP_ID_129819650 A-to-I Human chr3 - 38452611 38452611 38452611 AACATGGCAAAAACCTGTCTCTACTAAATAATACAAAAATTAGCTGGGCATGGTGACACACACCT AACATGGCAAAAACCTGTCTCTACTAAATAATGCAAAAATTAGCTGGGCATGGTGACACACACCT T C ACVR2B-AS1 Ensembl:ENSG00000229589 lincRNA exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs999358840 Functional Loss SNV dbSNP153 33..33 33 - - - 43727 RMVar_ID_43727 Human_SNP_ID_129823765 A-to-I Human chr3 + 38467560 38467560 38467560 GATCACTGGAGCCCAGAGTTTGAGACCATCTTAGGCAACGTAGTGAGACCCCATCTCTACAAAAA GATCACTGGAGCCCAGAGTTTGAGACCATCTTGGGCAACGTAGTGAGACCCCATCTCTACAAAAA A G ACVR2B Ensembl:ENSG00000114739 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1438859656 Functional Loss SNV dbSNP153 33..33 33 - - - 43728 RMVar_ID_43728 Human_SNP_ID_129823805 A-to-I Human chr3 + 38467641 38467641 38467641 GTGTGGTGGCATTGCACCTGTAAGTCCGAGCTACTTGGGAGGCTGAAGTGGGAGGATTGTTTGAG GTGTGGTGGCATTGCACCTGTAAGTCCGAGCTTCTTGGGAGGCTGAAGTGGGAGGATTGTTTGAG A T ACVR2B Ensembl:ENSG00000114739 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1241489376 Functional Loss SNV dbSNP153 33..33 33 - - - 43729 RMVar_ID_43729 Human_SNP_ID_129823824 A-to-I Human chr3 + 38467727 38467727 38467727 TGAGCTGTGATTGAGTCACTGTACTCCAGCCTAGGTCACAGAGCAAGACCCTGTGTCCAAAAAAA TGAGCTGTGATTGAGTCACTGTACTCCAGCCTGGGTCACAGAGCAAGACCCTGTGTCCAAAAAAA A G ACVR2B Ensembl:ENSG00000114739 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1004798698 Functional Loss SNV dbSNP153 33..33 33 - - - 43730 RMVar_ID_43730 Human_SNP_ID_129831784 A-to-I Human chr3 + 38498308 38498307 38498308 ATGAGAGGCTGGGCGTGGTGGCTCACACCTGTAATCCCAGTACTTTGGGAGGCTGAGGCGTTTGA ATGAGAGGCTGGGCGTGGTGGCTCACACCTGT_ATCCCAGTACTTTGGGAGGCTGAGGCGTTTGA TA T EXOG Ensembl:ENSG00000157036 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1185984979 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_279011,RMVar_hsa_circ_372713,RMVar_hsa_circ_217101 43731 RMVar_ID_43731 Human_SNP_ID_129832083 A-to-I Human chr3 + 38499750 38499750 38499750 CCTCAGCCTCCTGAGTAGCTGGGATTACAGGTATGTGCCACTATGCCCAACTAAAAGTATATCTT CCTCAGCCTCCTGAGTAGCTGGGATTACAGGTGTGTGCCACTATGCCCAACTAAAAGTATATCTT A G EXOG Ensembl:ENSG00000157036 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1300587899 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19117055 Human_Splice_Rec_411744,Human_Splice_Rec_411792,Human_Splice_Rec_411806 RMVar_hsa_circ_72568,RMVar_hsa_circ_279011,RMVar_hsa_circ_8964 43732 RMVar_ID_43732 Human_SNP_ID_129837659 A-to-I Human chr3 + 38524559 38524559 38524559 CTCACTATAGCCTCAAACTTCTGGGCTTAAGCAATCCTCCTGCCTCTGCCCCCTGAGCAGCTGGG CTCACTATAGCCTCAAACTTCTGGGCTTAAGCGATCCTCCTGCCTCTGCCCCCTGAGCAGCTGGG A G EXOG Ensembl:ENSG00000157036 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049373403 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1303860 43733 RMVar_ID_43733 Human_SNP_ID_129841262 A-to-I Human chr3 + 38540260 38540260 38540260 TTGAGTCTGGGAGTTCAAGGTTACAGTGAGCTATGATTGTGCCACTGCACTCCAGCCTGGGTGAC TTGAGTCTGGGAGTTCAAGGTTACAGTGAGCTGTGATTGTGCCACTGCACTCCAGCCTGGGTGAC A G EXOG Ensembl:ENSG00000157036 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs951403155 Functional Loss SNV dbSNP153 33..33 33 - - - 43734 RMVar_ID_43734 Human_SNP_ID_129841332 A-to-I Human chr3 + 38540615 38540615 38540615 AAAAACATAGCCAGGTGTGGTGGCTTACGCCTATAATCCCAGCATGCCTGGGAGGCTGAGGCAGG AAAAACATAGCCAGGTGTGGTGGCTTACGCCTGTAATCCCAGCATGCCTGGGAGGCTGAGGCAGG A G EXOG Ensembl:ENSG00000157036 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs549806576 Functional Loss SNV dbSNP153 33..33 33 - - - 43735 RMVar_ID_43735 Human_SNP_ID_129841362 A-to-I Human chr3 + 38540764 38540764 38540764 TGGTATGTTGGTACATGTCTGTAGTCCCAGCTACTTGGGAGACTGAGGTGGGAGGATTGCTTGAG TGGTATGTTGGTACATGTCTGTAGTCCCAGCTGCTTGGGAGACTGAGGTGGGAGGATTGCTTGAG A G EXOG Ensembl:ENSG00000157036 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1195414048 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4740800 43736 RMVar_ID_43736 Human_SNP_ID_130036233 A-to-I Human chr3 + 39333590 39333590 39333590 TTGTGCATGCCTGGCACAACATCAAGCCTGTGATTGTGTTTATTGATGATGTTGAACAAGTGGTA TTGTGCATGCCTGGCACAACATCAAGCCTGTGGTTGTGTTTATTGATGATGTTGAACAAGTGGTA A G CCR8 Ensembl:ENSG00000179934 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs574173549 Functional Loss SNV dbSNP153 33..33 33 - - - 43737 RMVar_ID_43737 Human_SNP_ID_130042051 A-to-I Human chr3 - 39358577 39358577 39358577 GTGGACTTGCCCAAATCTACATGTCCAATGACAACAATGTTGATATGAGTCTTTTCCATTCCCAT GTGGACTTGCCCAAATCTACATGTCCAATGACGACAATGTTGATATGAGTCTTTTCCATTCCCAT T C AC104850.2 Ensembl:ENSG00000287780 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355491294 Functional Loss SNV dbSNP153 33..33 33 - - - 43738 RMVar_ID_43738 Human_SNP_ID_130050527 A-to-I Human chr3 + 39393523 39393522 39393524 TAACCTAGATAATTTTTTCTTTTTTTTGAGACAGAGTCTTGCCCTGTCACTCAGGCTGGAGTGCA TAACCTAGATAATTTTTTCTTTTTTTTGAGAC__AGTCTTGCCCTGTCACTCAGGCTGGAGTGCA CAG C SLC25A38 Ensembl:ENSG00000144659 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs752839368 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_34939,RMVar_hsa_circ_296254,RMVar_hsa_circ_217123 43739 RMVar_ID_43739 Human_SNP_ID_130054736 A-to-I Human chr3 + 39409101 39409100 39409101 GCCGAGACTCTGTCTCAAAAAAAAAAAAAAAGAAAATAGAAAACTCAAACTCCACTGTTAAGAGA GCCGAGACTCTGTCTCAAAAAAAAAAAAAAAG_AAATAGAAAACTCAAACTCCACTGTTAAGAGA GA G RPSA Ensembl:ENSG00000168028 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs145906801 Functional Loss DEL dbSNP153 33..33 33 - - - 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 43740 RMVar_ID_43740 Human_SNP_ID_130054737 A-to-I Human chr3 + 39409101 39409101 39409101 GCCGAGACTCTGTCTCAAAAAAAAAAAAAAAGAAAATAGAAAACTCAAACTCCACTGTTAAGAGA GCCGAGACTCTGTCTCAAAAAAAAAAAAAAAGGAAATAGAAAACTCAAACTCCACTGTTAAGAGA A G RPSA Ensembl:ENSG00000168028 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs79217109 Functional Loss SNV dbSNP153 33..33 33 - - - 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 43741 RMVar_ID_43741 Human_SNP_ID_130054858 A-to-I Human chr3 + 39409295 39409295 39409295 GTGATATCGGCTCATTGCAGCCTTTGCCTCCTAAGCTCAAGGGATTCTCCTGCCTCATCCTCCCG GTGATATCGGCTCATTGCAGCCTTTGCCTCCTTAGCTCAAGGGATTCTCCTGCCTCATCCTCCCG A T RPSA Ensembl:ENSG00000168028 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs926352091 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17574050 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 43742 RMVar_ID_43742 Human_SNP_ID_130055065 A-to-I Human chr3 + 39410042 39410042 39410042 GTCTCAGCTGAGGCTAAGGTGGGAAGATTGCTAGAACACAGGAGGTTGAGGCAGCAGGGAGCCAA GTCTCAGCTGAGGCTAAGGTGGGAAGATTGCTGGAACACAGGAGGTTGAGGCAGCAGGGAGCCAA A G RPSA Ensembl:ENSG00000168028 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1026103893 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7193122,Human_RBP_ID_14812413 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 43743 RMVar_ID_43743 Human_SNP_ID_130055066 A-to-I Human chr3 + 39410049 39410042 39410050 CTGAGGCTAAGGTGGGAAGATTGCTAGAACACAGGAGGTTGAGGCAGCAGGGAGCCAAGACTGTC CTGAGGCTAAGGTGGGAAGATTGCTA________GAGGTTGAGGCAGCAGGGAGCCAAGACTGTC AGAACACAG A RPSA Ensembl:ENSG00000168028 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1399931184 Functional Loss DEL dbSNP153 27..34 33 - - - Human_RBP_ID_7193122,Human_RBP_ID_14812413 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 43744 RMVar_ID_43744 Human_SNP_ID_130110850 A-to-I Human chr3 - 39644238 39644238 39644238 TACTCCTTCAATCCTAAATAACTGCCTAGCCAAAGGGGAGCAAAATGCTGCAGCTGGGGTGGGAA TACTCCTTCAATCCTAAATAACTGCCTAGCCAGAGGGGAGCAAAATGCTGCAGCTGGGGTGGGAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs529087039 Functional Loss SNV dbSNP153 33..33 33 - - - 43745 RMVar_ID_43745 Human_SNP_ID_130110857 A-to-I Human chr3 - 39644279 39644279 39644279 TTTGTGGCAGTGATGAAATCTGGCCCAAAGAAAACACTTTTTACTCCTTCAATCCTAAATAACTG TTTGTGGCAGTGATGAAATCTGGCCCAAAGAAGACACTTTTTACTCCTTCAATCCTAAATAACTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1192894733 Functional Loss SNV dbSNP153 33..33 33 - - - 43746 RMVar_ID_43746 Human_SNP_ID_130212960 A-to-I Human chr3 + 40070623 40070623 40070623 TCAGCGATGGCATTAGATTCTCATAGGAGCACAAACCCTATTGTGAATTGTGTGTGCGAGGGATC TCAGCGATGGCATTAGATTCTCATAGGAGCACGAACCCTATTGTGAATTGTGTGTGCGAGGGATC A G MYRIP Ensembl:ENSG00000170011 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1398116479 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63379,RMVar_hsa_circ_62393 43747 RMVar_ID_43747 Human_SNP_ID_130304592 A-to-I Human chr3 + 40459442 40459441 40459442 CTAGCTTACATTTAAGTGAGGCAGTGAATAGCAGTTCTTTTTTGACATGAAAATTAAAACACTTT CTAGCTTACATTTAAGTGAGGCAGTGAATAGTGGTTCTTTTTTGACATGAAAATTAAAACACTTT CA TG RPL14 Ensembl:ENSG00000188846 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs386660393 Functional Loss MNV dbSNP153 32..33 33 - - - Human_RBP_ID_14813160 RMVar_hsa_circ_78228,RMVar_hsa_circ_95151,RMVar_hsa_circ_217145,RMVar_hsa_circ_84138,RMVar_hsa_circ_217146,RMVar_hsa_circ_71933,RMVar_hsa_circ_217149,RMVar_hsa_circ_217151,RMVar_hsa_circ_93463,RMVar_hsa_circ_117953,RMVar_hsa_circ_217152 43748 RMVar_ID_43748 Human_SNP_ID_130304593 A-to-I Human chr3 + 40459442 40459442 40459442 CTAGCTTACATTTAAGTGAGGCAGTGAATAGCAGTTCTTTTTTGACATGAAAATTAAAACACTTT CTAGCTTACATTTAAGTGAGGCAGTGAATAGCGGTTCTTTTTTGACATGAAAATTAAAACACTTT A G RPL14 Ensembl:ENSG00000188846 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6766936 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14813160 RMVar_hsa_circ_78228,RMVar_hsa_circ_95151,RMVar_hsa_circ_217145,RMVar_hsa_circ_84138,RMVar_hsa_circ_217146,RMVar_hsa_circ_71933,RMVar_hsa_circ_217149,RMVar_hsa_circ_217151,RMVar_hsa_circ_93463,RMVar_hsa_circ_117953,RMVar_hsa_circ_217152 43749 RMVar_ID_43749 Human_SNP_ID_130304695 A-to-I Human chr3 + 40459730 40459730 40459730 ACAAAAAAAAAATATTCCGGGCATGGTGGCGGACACCTGTAGTCCCAGCTACTTCAGAGGCTGAG ACAAAAAAAAAATATTCCGGGCATGGTGGCGGGCACCTGTAGTCCCAGCTACTTCAGAGGCTGAG A G RPL14 Ensembl:ENSG00000188846 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4973905 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78228,RMVar_hsa_circ_95151,RMVar_hsa_circ_217145,RMVar_hsa_circ_84138,RMVar_hsa_circ_217146,RMVar_hsa_circ_71933,RMVar_hsa_circ_217149,RMVar_hsa_circ_217151,RMVar_hsa_circ_93463,RMVar_hsa_circ_117953,RMVar_hsa_circ_217152 43750 RMVar_ID_43750 Human_SNP_ID_130305065 A-to-I Human chr3 + 40460662 40460662 40460662 TTGACACGGAGTCTCACTTTGTCACCCAGGCTAGAGTGCAGTGACGCAATCTTGACTCACTGCAA TTGACACGGAGTCTCACTTTGTCACCCAGGCTGGAGTGCAGTGACGCAATCTTGACTCACTGCAA A G RPL14 Ensembl:ENSG00000188846 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs779159718 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78228,RMVar_hsa_circ_95151,RMVar_hsa_circ_217145,RMVar_hsa_circ_84138,RMVar_hsa_circ_217146,RMVar_hsa_circ_71933,RMVar_hsa_circ_217149,RMVar_hsa_circ_217151,RMVar_hsa_circ_93463,RMVar_hsa_circ_117953,RMVar_hsa_circ_217152 43751 RMVar_ID_43751 Human_SNP_ID_130305761 A-to-I Human chr3 + 40462441 40462441 40462441 TTCTGTTGCTCAGGCCGGACTGCAGTGGCGCTATCTCGGCTCACTGTAAGTTCCACCTCCCGGGT TTCTGTTGCTCAGGCCGGACTGCAGTGGCGCTCTCTCGGCTCACTGTAAGTTCCACCTCCCGGGT A C RPL14 Ensembl:ENSG00000188846 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1308008166 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8572023,Human_RBP_ID_14813239 43752 RMVar_ID_43752 Human_SNP_ID_130305762 A-to-I Human chr3 + 40462441 40462441 40462441 TTCTGTTGCTCAGGCCGGACTGCAGTGGCGCTATCTCGGCTCACTGTAAGTTCCACCTCCCGGGT TTCTGTTGCTCAGGCCGGACTGCAGTGGCGCTGTCTCGGCTCACTGTAAGTTCCACCTCCCGGGT A G RPL14 Ensembl:ENSG00000188846 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1308008166 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8572023,Human_RBP_ID_14813239 43753 RMVar_ID_43753 Human_SNP_ID_130305955 A-to-I Human chr3 + 40462950 40462950 40462950 TTTATTTATTTATTTTTTTTTTTTGGAGACAGAGTCTTGCTGTGTTGCCCAGGCTGGAGTGCAGT TTTATTTATTTATTTTTTTTTTTTGGAGACAGTGTCTTGCTGTGTTGCCCAGGCTGGAGTGCAGT A T RPL14 Ensembl:ENSG00000188846 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs975010732 Functional Loss SNV dbSNP153 33..33 33 - - - 43754 RMVar_ID_43754 Human_SNP_ID_130306003 A-to-I Human chr3 + 40463095 40463095 40463095 GCCCACCACCATGCCCAGCTAATTTTTTTTGTAGAGACTGGGTTTCACTATGTTGGCCAGGCTGG GCCCACCACCATGCCCAGCTAATTTTTTTTGTGGAGACTGGGTTTCACTATGTTGGCCAGGCTGG A G RPL14 Ensembl:ENSG00000188846 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1227096774 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2783780,Human_RBP_ID_3707053,Human_RBP_ID_14813268 43755 RMVar_ID_43755 Human_SNP_ID_130306076 A-to-I Human chr3 + 40463335 40463335 40463335 CTCAAGCGGTTCTCCTGCTCAGCCTTCTGAGTAGTTGGGACTATAGGTGTGTGCCACCACGTCTG CTCAAGCGGTTCTCCTGCTCAGCCTTCTGAGTCGTTGGGACTATAGGTGTGTGCCACCACGTCTG A C RPL14 Ensembl:ENSG00000188846 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1488611865 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_601437,Human_RBP_ID_7193434,Human_RBP_ID_14813281 43756 RMVar_ID_43756 Human_SNP_ID_130306106 A-to-I Human chr3 + 40463440 40463440 40463440 GTTGGCCATGCTGGTCTCGAGCTCCTGACCTCAGGTGATACACCCGCCTTGGCCTCCCAAAGTGC GTTGGCCATGCTGGTCTCGAGCTCCTGACCTCGGGTGATACACCCGCCTTGGCCTCCCAAAGTGC A G RPL14 Ensembl:ENSG00000188846 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1311373537 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14813288 43757 RMVar_ID_43757 Human_SNP_ID_130306290 A-to-I Human chr3 + 40464039 40464038 40464039 TTGCCCAGGCTGGAATGTAGTGGCACGATCTCAGCTCACTGCGACCTCCACCTCCCAGGTTCAAG TTGCCCAGGCTGGAATGTAGTGGCACGATCTC_GCTCACTGCGACCTCCACCTCCCAGGTTCAAG CA C RPL14 Ensembl:ENSG00000188846 Protein coding 3'UTR GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,30559470,31158229,31158229 RNA-Seq:(High) rs1163189541 Functional Loss DEL dbSNP153 33..33 33 - - - 43758 RMVar_ID_43758 Human_SNP_ID_130306291 A-to-I Human chr3 + 40464039 40464039 40464039 TTGCCCAGGCTGGAATGTAGTGGCACGATCTCAGCTCACTGCGACCTCCACCTCCCAGGTTCAAG TTGCCCAGGCTGGAATGTAGTGGCACGATCTCCGCTCACTGCGACCTCCACCTCCCAGGTTCAAG A C RPL14 Ensembl:ENSG00000188846 Protein coding 3'UTR GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,30559470,31158229,31158229 RNA-Seq:(High) rs1430567063 Functional Loss SNV dbSNP153 33..33 33 - - - 43759 RMVar_ID_43759 Human_SNP_ID_130306299 A-to-I Human chr3 + 40464063 40464063 40464063 ACGATCTCAGCTCACTGCGACCTCCACCTCCCAGGTTCAAGTTGTTCTGCCTCAGCCTCCCAAGT ACGATCTCAGCTCACTGCGACCTCCACCTCCCCGGTTCAAGTTGTTCTGCCTCAGCCTCCCAAGT A C RPL14 Ensembl:ENSG00000188846 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs1205437955 Functional Loss SNV dbSNP153 33..33 33 - - - 43760 RMVar_ID_43760 Human_SNP_ID_130306311 A-to-I Human chr3 + 40464099 40464099 40464099 TCAAGTTGTTCTGCCTCAGCCTCCCAAGTAGCAGGGGTTAAATGCGTGTACCACCATGCCCCTCT TCAAGTTGTTCTGCCTCAGCCTCCCAAGTAGCTGGGGTTAAATGCGTGTACCACCATGCCCCTCT A T RPL14 Ensembl:ENSG00000188846 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1029015554 Functional Loss SNV dbSNP153 33..33 33 - - - 43761 RMVar_ID_43761 Human_SNP_ID_130306331 A-to-I Human chr3 + 40464143 40464143 40464143 CGTGTACCACCATGCCCCTCTAATATTGTATTAGAGATGGGGTTTTGCCATGTCAGCCAGACTGG CGTGTACCACCATGCCCCTCTAATATTGTATTGGAGATGGGGTTTTGCCATGTCAGCCAGACTGG A G RPL14 Ensembl:ENSG00000188846 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs766184110 Functional Loss SNV dbSNP153 33..33 33 - - - 43762 RMVar_ID_43762 Human_SNP_ID_130306343 A-to-I Human chr3 + 40464194 40464194 40464194 GTCAGCCAGACTGGTCTTGAACTCCTGACCTCAGGTGATCTGTCCGCCTTGGCCTCCCAAAGTGC GTCAGCCAGACTGGTCTTGAACTCCTGACCTCGGGTGATCTGTCCGCCTTGGCCTCCCAAAGTGC A G RPL14 Ensembl:ENSG00000188846 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1405416714 Functional Loss SNV dbSNP153 33..33 33 - - - 43763 RMVar_ID_43763 Human_SNP_ID_130306350 A-to-I Human chr3 + 40464220 40464220 40464220 GACCTCAGGTGATCTGTCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCT GACCTCAGGTGATCTGTCCGCCTTGGCCTCCCGAAGTGCTGGGATTACAGGCGTGAGCCACCGCT A G RPL14 Ensembl:ENSG00000188846 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1268685489 Functional Loss SNV dbSNP153 33..33 33 - - - 43764 RMVar_ID_43764 Human_SNP_ID_130306351 A-to-I Human chr3 + 40464220 40464220 40464220 GACCTCAGGTGATCTGTCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCT GACCTCAGGTGATCTGTCCGCCTTGGCCTCCCTAAGTGCTGGGATTACAGGCGTGAGCCACCGCT A T RPL14 Ensembl:ENSG00000188846 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1268685489 Functional Loss SNV dbSNP153 33..33 33 - - - 43765 RMVar_ID_43765 Human_SNP_ID_130306373 A-to-I Human chr3 + 40464294 40464294 40464294 GAATACATTTTAAATAAATTTGTTTCCTAACCAAAAGCTAGCTTCAGGCGTCACTGGGGTAAAGG GAATACATTTTAAATAAATTTGTTTCCTAACCGAAAGCTAGCTTCAGGCGTCACTGGGGTAAAGG A G RPL14 Ensembl:ENSG00000188846 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1050358233 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9140430 43766 RMVar_ID_43766 Human_SNP_ID_130306850 A-to-I Human chr3 + 40465962 40465962 40465962 CCTGTAATCCCAGCACTATGGGAGGCTGAGGCAGGCGGATCACCTGAGGTCAGGGGTCCGAGACC CCTGTAATCCCAGCACTATGGGAGGCTGAGGCGGGCGGATCACCTGAGGTCAGGGGTCCGAGACC A G RPL14 Ensembl:ENSG00000188846 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1365278457 Functional Loss SNV dbSNP153 33..33 33 - - - 43767 RMVar_ID_43767 Human_SNP_ID_130306858 A-to-I Human chr3 + 40465981 40465980 40465981 GGGAGGCTGAGGCAGGCGGATCACCTGAGGTCAGGGGTCCGAGACCAGCTTGGCCAACATGGTGA GGGAGGCTGAGGCAGGCGGATCACCTGAGGTC_GGGGTCCGAGACCAGCTTGGCCAACATGGTGA CA C RPL14 Ensembl:ENSG00000188846 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1360876610 Functional Loss DEL dbSNP153 33..33 33 - - - 43768 RMVar_ID_43768 Human_SNP_ID_130306877 A-to-I Human chr3 + 40466039 40466039 40466039 ATGGTGAAACCCCGTCTTTACTAAAAATACAAAAATTAGACAGGCATGGTGGAGCATGCCTGTAA ATGGTGAAACCCCGTCTTTACTAAAAATACAACAATTAGACAGGCATGGTGGAGCATGCCTGTAA A C RPL14 Ensembl:ENSG00000188846 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1018413309 Functional Loss SNV dbSNP153 33..33 33 - - - 43769 RMVar_ID_43769 Human_SNP_ID_130308196 A-to-I Human chr3 + 40470639 40470639 40470639 ACAGTCCACCTGCCTTGGCCTCCCAAGGTGCTAGGATTACAGGTGTGAGCTACTGCGCCTGGCTG ACAGTCCACCTGCCTTGGCCTCCCAAGGTGCTGGGATTACAGGTGTGAGCTACTGCGCCTGGCTG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1475292123 Functional Loss SNV dbSNP153 33..33 33 - - - 43770 RMVar_ID_43770 Human_SNP_ID_130323677 A-to-I Human chr3 + 40533189 40533189 40533189 TTGAGAAAGGGTCTTGCTCTGTCACCCAGGCTAGAGTGCGGTGGTGTGATCTTGGCTCACTGCAA TTGAGAAAGGGTCTTGCTCTGTCACCCAGGCTGGAGTGCGGTGGTGTGATCTTGGCTCACTGCAA A G ZNF621 Ensembl:ENSG00000172888 Protein coding 3'UTR GSE38233;GSE107867 cultured B-cells;ASD brains,frontal_cortex - 24183664,30559470 RNA-Seq:(High) rs1376386851 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_601548,Human_RBP_ID_14814559,Human_RBP_ID_27317893 Human_miRNA_ID_113024,Human_miRNA_ID_1968219 RMVar_hsa_circ_217161,RMVar_hsa_circ_126844 43771 RMVar_ID_43771 Human_SNP_ID_130324357 A-to-I Human chr3 + 40536236 40536236 40536236 TTGCCTCAGCCTCCTGAGTAGTGTGTGCCACCACGCCCAGCTAATTTTTTAATTTTTAGTAGAGA TTGCCTCAGCCTCCTGAGTAGTGTGTGCCACCGCGCCCAGCTAATTTTTTAATTTTTAGTAGAGA A G ZNF621 Ensembl:ENSG00000172888 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1408820677 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1808088 RMVar_hsa_circ_217161,RMVar_hsa_circ_126844 43772 RMVar_ID_43772 Human_SNP_ID_130324375 A-to-I Human chr3 + 40536278 40536278 40536278 AATTTTTTAATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGG AATTTTTTAATTTTTAGTAGAGACAGGGTTTCGCCATGTTGGCCAGGCTGGTCTTGAACTCCTGG A G ZNF621 Ensembl:ENSG00000172888 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1213451512 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_217161,RMVar_hsa_circ_126844 43773 RMVar_ID_43773 Human_SNP_ID_130324376 A-to-I Human chr3 + 40536281 40536281 40536281 TTTTTAATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGGCAG TTTTTAATTTTTAGTAGAGACAGGGTTTCACCGTGTTGGCCAGGCTGGTCTTGAACTCCTGGCAG A G ZNF621 Ensembl:ENSG00000172888 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1428664255 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14814706 RMVar_hsa_circ_217161,RMVar_hsa_circ_126844 43774 RMVar_ID_43774 Human_SNP_ID_130324589 A-to-I Human chr3 + 40537324 40537324 40537324 CCAGGGAACACATGAACGATAATAAAGTGGCCAGGTGCAGTGGCTGACACCTAGAATCCCAGCAC CCAGGGAACACATGAACGATAATAAAGTGGCCGGGTGCAGTGGCTGACACCTAGAATCCCAGCAC A G ZNF621 Ensembl:ENSG00000172888 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6775029 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247814,Human_RBP_ID_18005353 RMVar_hsa_circ_217161,RMVar_hsa_circ_126844 43775 RMVar_ID_43775 Human_SNP_ID_130324809 A-to-I Human chr3 + 40538251 40538251 40538251 AAAAAAGAATTCTGTCAGGTGTGGTGGCTCACACTTGTAATCCCAACACTTTGGGAGGCCAAGGC AAAAAAGAATTCTGTCAGGTGTGGTGGCTCACGCTTGTAATCCCAACACTTTGGGAGGCCAAGGC A G ZNF621 Ensembl:ENSG00000172888 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1015676993 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14814794 RMVar_hsa_circ_217161,RMVar_hsa_circ_126844 43776 RMVar_ID_43776 Human_SNP_ID_130482717 A-to-I Human chr3 + 41221483 41221483 41221483 TTTGCCTCAGCCTCCCCAGTGGCTAGGACTACAGGCACATACTACCACACCTGGCTAATTTTTAA TTTGCCTCAGCCTCCCCAGTGGCTAGGACTACTGGCACATACTACCACACCTGGCTAATTTTTAA A T CTNNB1 Ensembl:ENSG00000168036 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1422088943 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122575,RMVar_hsa_circ_265301,RMVar_hsa_circ_217163 43777 RMVar_ID_43777 Human_SNP_ID_130519278 A-to-I Human chr3 - 41369678 41369678 41369678 GGGATTCTCATTCCTCAGCCTCCTGAGTAGCTAGCATTACAGGCGGCCACCACCATCCTGGCTAA GGGATTCTCATTCCTCAGCCTCCTGAGTAGCTGGCATTACAGGCGGCCACCACCATCCTGGCTAA T C ULK4 Ensembl:ENSG00000168038 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs959078979 Functional Loss SNV dbSNP153 33..33 33 - - - 43778 RMVar_ID_43778 Human_SNP_ID_130608516 A-to-I Human chr3 - 41702975 41702975 41702975 GTGGTGTGTGCCTGTAGTCCCAGCTACTCGGGAGGCTGGGGCAGGAGAGTCGCTTGAACCTGGGA GTGGTGTGTGCCTGTAGTCCCAGCTACTCGGGGGGCTGGGGCAGGAGAGTCGCTTGAACCTGGGA T C ULK4 Ensembl:ENSG00000168038 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1016088269 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7218,RMVar_hsa_circ_308464,RMVar_hsa_circ_32034,RMVar_hsa_circ_19926,RMVar_hsa_circ_5453,RMVar_hsa_circ_6400,RMVar_hsa_circ_38853,RMVar_hsa_circ_50293,RMVar_hsa_circ_349737,RMVar_hsa_circ_56894,RMVar_hsa_circ_39074,RMVar_hsa_circ_17183,RMVar_hsa_circ_12423,RMVar_hsa_circ_13976,RMVar_hsa_circ_59781,RMVar_hsa_circ_300712,RMVar_hsa_circ_318905,RMVar_hsa_circ_277757,RMVar_hsa_circ_280897,RMVar_hsa_circ_342010,RMVar_hsa_circ_342119,RMVar_hsa_circ_62003,RMVar_hsa_circ_39200,RMVar_hsa_circ_6545,RMVar_hsa_circ_4959,RMVar_hsa_circ_37364,RMVar_hsa_circ_288666,RMVar_hsa_circ_321378,RMVar_hsa_circ_326987,RMVar_hsa_circ_50970,RMVar_hsa_circ_7362,RMVar_hsa_circ_281460,RMVar_hsa_circ_293871,RMVar_hsa_circ_344033,RMVar_hsa_circ_366451,RMVar_hsa_circ_278196 43779 RMVar_ID_43779 Human_SNP_ID_130652786 A-to-I Human chr3 - 41856902 41856901 41856902 GCTTAGTCTTTTGTTTTGTTTTGTTTTATACAAGGTCTCACTCTGTCACCCAGGCTGTGGTGCAG GCTTAGTCTTTTGTTTTGTTTTGTTTTATACA_GGTCTCACTCTGTCACCCAGGCTGTGGTGCAG CT C ULK4 Ensembl:ENSG00000168038 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs768542443 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_308464,RMVar_hsa_circ_32034,RMVar_hsa_circ_6400,RMVar_hsa_circ_50293,RMVar_hsa_circ_349737,RMVar_hsa_circ_56894,RMVar_hsa_circ_39074,RMVar_hsa_circ_17183,RMVar_hsa_circ_300712,RMVar_hsa_circ_277757,RMVar_hsa_circ_280897,RMVar_hsa_circ_62003,RMVar_hsa_circ_4959,RMVar_hsa_circ_37364,RMVar_hsa_circ_321378,RMVar_hsa_circ_344033,RMVar_hsa_circ_55948,RMVar_hsa_circ_6234,RMVar_hsa_circ_5762,RMVar_hsa_circ_85959,RMVar_hsa_circ_217194,RMVar_hsa_circ_364383,RMVar_hsa_circ_16397,RMVar_hsa_circ_16031,RMVar_hsa_circ_320232,RMVar_hsa_circ_52324,RMVar_hsa_circ_32560,RMVar_hsa_circ_37583,RMVar_hsa_circ_89953,RMVar_hsa_circ_327525,RMVar_hsa_circ_327863,RMVar_hsa_circ_217200,RMVar_hsa_circ_325810,RMVar_hsa_circ_46190,RMVar_hsa_circ_58915,RMVar_hsa_circ_343893,RMVar_hsa_circ_325407,RMVar_hsa_circ_316700,RMVar_hsa_circ_363070,RMVar_hsa_circ_50665,RMVar_hsa_circ_338845,RMVar_hsa_circ_217203,RMVar_hsa_circ_16519,RMVar_hsa_circ_217202 43780 RMVar_ID_43780 Human_SNP_ID_130652787 A-to-I Human chr3 - 41856902 41856902 41856902 GCTTAGTCTTTTGTTTTGTTTTGTTTTATACAAGGTCTCACTCTGTCACCCAGGCTGTGGTGCAG GCTTAGTCTTTTGTTTTGTTTTGTTTTATACAGGGTCTCACTCTGTCACCCAGGCTGTGGTGCAG T C ULK4 Ensembl:ENSG00000168038 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs577184486 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_308464,RMVar_hsa_circ_32034,RMVar_hsa_circ_6400,RMVar_hsa_circ_50293,RMVar_hsa_circ_349737,RMVar_hsa_circ_56894,RMVar_hsa_circ_39074,RMVar_hsa_circ_17183,RMVar_hsa_circ_300712,RMVar_hsa_circ_277757,RMVar_hsa_circ_280897,RMVar_hsa_circ_62003,RMVar_hsa_circ_4959,RMVar_hsa_circ_37364,RMVar_hsa_circ_321378,RMVar_hsa_circ_344033,RMVar_hsa_circ_55948,RMVar_hsa_circ_6234,RMVar_hsa_circ_5762,RMVar_hsa_circ_85959,RMVar_hsa_circ_217194,RMVar_hsa_circ_364383,RMVar_hsa_circ_16397,RMVar_hsa_circ_16031,RMVar_hsa_circ_320232,RMVar_hsa_circ_52324,RMVar_hsa_circ_32560,RMVar_hsa_circ_37583,RMVar_hsa_circ_89953,RMVar_hsa_circ_327525,RMVar_hsa_circ_327863,RMVar_hsa_circ_217200,RMVar_hsa_circ_325810,RMVar_hsa_circ_46190,RMVar_hsa_circ_58915,RMVar_hsa_circ_343893,RMVar_hsa_circ_325407,RMVar_hsa_circ_316700,RMVar_hsa_circ_363070,RMVar_hsa_circ_50665,RMVar_hsa_circ_338845,RMVar_hsa_circ_217203,RMVar_hsa_circ_16519,RMVar_hsa_circ_217202 43781 RMVar_ID_43781 Human_SNP_ID_130695023 A-to-I Human chr3 + 42016996 42016996 42016996 AAATGGACTCTGACCACTGGCTGCGGTGGCTCACACCTGTAATCCTAGCACTTTGGGAGGCCAAG AAATGGACTCTGACCACTGGCTGCGGTGGCTCGCACCTGTAATCCTAGCACTTTGGGAGGCCAAG A G TRAK1 Ensembl:ENSG00000182606 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1462116602 Functional Loss SNV dbSNP153 33..33 33 - - - 43782 RMVar_ID_43782 Human_SNP_ID_130698234 A-to-I Human chr3 + 42029463 42029463 42029463 GGGGTCTCACTATGTTGCCCAGGGTAGTCTTGAACTCCTGAGCTCAAGGCATCCTCCCTCCTTGT GGGGTCTCACTATGTTGCCCAGGGTAGTCTTGCACTCCTGAGCTCAAGGCATCCTCCCTCCTTGT A C TRAK1 Ensembl:ENSG00000182606 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1240040417 Functional Loss SNV dbSNP153 33..33 33 - - - 43783 RMVar_ID_43783 Human_SNP_ID_130698459 A-to-I Human chr3 + 42030306 42030302 42030306 CCCTTTTGAGCTCAGGAGCGCAAGGCAGCAGTAAGCTGTGATCTCGCCACTGTACTCCAGCCTGT CCCTTTTGAGCTCAGGAGCGCAAGGCAGC____AGCTGTGATCTCGCCACTGTACTCCAGCCTGT CAGTA C TRAK1 Ensembl:ENSG00000182606 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1329801487 Functional Loss DEL dbSNP153 30..33 33 - - - 43784 RMVar_ID_43784 Human_SNP_ID_130698799 A-to-I Human chr3 + 42031139 42031139 42031139 CTCACTGCAGCCTCCACCTCCCAGATTCGAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGG CTCACTGCAGCCTCCACCTCCCAGATTCGAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGG A G TRAK1 Ensembl:ENSG00000182606 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs199899706 Functional Loss SNV dbSNP153 33..33 33 - - - 43785 RMVar_ID_43785 Human_SNP_ID_130704785 A-to-I Human chr3 + 42055604 42055604 42055604 CCCATATCAGCTTCCTGAGTAGCTGAGATCACAGGCGTGTGCCACCATGCTCTGCTAATTTTTTA CCCATATCAGCTTCCTGAGTAGCTGAGATCACGGGCGTGTGCCACCATGCTCTGCTAATTTTTTA A G TRAK1 Ensembl:ENSG00000182606 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs921916898 Functional Loss SNV dbSNP153 33..33 33 - - - 43786 RMVar_ID_43786 Human_SNP_ID_130708729 A-to-I Human chr3 + 42071665 42071665 42071665 GGGAAATGGAGGTTGCAGTGAGCTGAGATCGCACTATTGCACTCTAGTCTGGATGACAAGCGAAA GGGAAATGGAGGTTGCAGTGAGCTGAGATCGCGCTATTGCACTCTAGTCTGGATGACAAGCGAAA A G TRAK1 Ensembl:ENSG00000182606 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1488204816 Functional Loss SNV dbSNP153 33..33 33 - - - 43787 RMVar_ID_43787 Human_SNP_ID_130709633 A-to-I Human chr3 + 42075218 42075218 42075218 TGAGGTCTGGCTGGGTGTGGTGGCTCACGCCTATAATCCCAGCTACTCTGGAGGCTGAGGTATGA TGAGGTCTGGCTGGGTGTGGTGGCTCACGCCTGTAATCCCAGCTACTCTGGAGGCTGAGGTATGA A G TRAK1 Ensembl:ENSG00000182606 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs916109216 Functional Loss SNV dbSNP153 33..33 33 - - - 43788 RMVar_ID_43788 Human_SNP_ID_130714112 A-to-I Human chr3 + 42092820 42092820 42092820 ATTGCCCAGGCTGGTTTTGAATTCCTGGGCTCAAGTGATCCCCCTGCCTCGGCCTCCCAAAGTGC ATTGCCCAGGCTGGTTTTGAATTCCTGGGCTCGAGTGATCCCCCTGCCTCGGCCTCCCAAAGTGC A G TRAK1 Ensembl:ENSG00000182606 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1464735100 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56960,RMVar_hsa_circ_289985,RMVar_hsa_circ_69649,RMVar_hsa_circ_77431,RMVar_hsa_circ_217215,RMVar_hsa_circ_217216 43789 RMVar_ID_43789 Human_SNP_ID_130809016 A-to-I Human chr3 + 42469621 42469621 42469621 CATCTTGGCTCCTGTGGAGGCCTGCTGGTAACAGGACTTATAAAAGGAAATATGTCTGGAAGACT CATCTTGGCTCCTGTGGAGGCCTGCTGGTAACCGGACTTATAAAAGGAAATATGTCTGGAAGACT A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1369186888 Functional Loss SNV dbSNP153 33..33 33 - - - 43790 RMVar_ID_43790 Human_SNP_ID_130809017 A-to-I Human chr3 + 42469621 42469621 42469621 CATCTTGGCTCCTGTGGAGGCCTGCTGGTAACAGGACTTATAAAAGGAAATATGTCTGGAAGACT CATCTTGGCTCCTGTGGAGGCCTGCTGGTAACGGGACTTATAAAAGGAAATATGTCTGGAAGACT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1369186888 Functional Loss SNV dbSNP153 33..33 33 - - - 43791 RMVar_ID_43791 Human_SNP_ID_130837812 A-to-I Human chr3 + 42587615 42587611 42587615 AAAATTAGCCGGGCGTGATGGCGAGCGCCTGTAGTCCCAGCTACTGGGGAAGCTGAGGCAGGAGA AAAATTAGCCGGGCGTGATGGCGAGCGCC____GTCCCAGCTACTGGGGAAGCTGAGGCAGGAGA CTGTA C SS18L2 Ensembl:ENSG00000008324 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1398905966 Functional Loss DEL dbSNP153 30..33 33 - - - 43792 RMVar_ID_43792 Human_SNP_ID_130837900 A-to-I Human chr3 + 42587962 42587962 42587962 GGGCGTGGTGGTGCATGCCTGTAATCCTGGCCACTTGGGAGGCTGAGGCAGGAGAATTGCTGGAA GGGCGTGGTGGTGCATGCCTGTAATCCTGGCCTCTTGGGAGGCTGAGGCAGGAGAATTGCTGGAA A T SS18L2 Ensembl:ENSG00000008324 Protein coding intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1197091718 Functional Loss SNV dbSNP153 33..33 33 - - - 43793 RMVar_ID_43793 Human_SNP_ID_130837962 A-to-I Human chr3 + 42588218 42588218 42588218 GAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATAGAGAAACCCCATCTCTACTAAAAATACAAA GAGGTCAGGAGTTCAAGACCAGCCTGGCCAACGTAGAGAAACCCCATCTCTACTAAAAATACAAA A G SS18L2 Ensembl:ENSG00000008324 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1296927536 Functional Loss SNV dbSNP153 33..33 33 - - - 43794 RMVar_ID_43794 Human_SNP_ID_130841927 A-to-I Human chr3 + 42602855 42602855 42602855 CCTGGCCTACATGGCGAAACCCCATCTCTACAAAAAATAAAAAAATTAGCTGGGCATGGTGGCTC CCTGGCCTACATGGCGAAACCCCATCTCTACAGAAAATAAAAAAATTAGCTGGGCATGGTGGCTC A G NKTR Ensembl:ENSG00000114857 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1003256328 Functional Loss SNV dbSNP153 33..33 33 - - - 43795 RMVar_ID_43795 Human_SNP_ID_130849197 A-to-I Human chr3 - 42633172 42633172 42633172 AGCCAAGCATAGTGGTATACGCCCGTAGTCCTAGCTACTCAGGAGGCTGATGCAGAAAGATCTCT AGCCAAGCATAGTGGTATACGCCCGTAGTCCTGGCTACTCAGGAGGCTGATGCAGAAAGATCTCT T C AC006059.1 Ensembl:ENSG00000230084 lincRNA intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1222076036 Functional Loss SNV dbSNP153 33..33 33 - - - 43796 RMVar_ID_43796 Human_SNP_ID_130887248 A-to-I Human chr3 - 42783859 42783859 42783859 GTTGGCCAGGCTGATCTTGAATTCCTGACCTCAGGTTATCCACCTGCCTCGGCCTCCCAAAGTGC GTTGGCCAGGCTGATCTTGAATTCCTGACCTCGGGTTATCCACCTGCCTCGGCCTCCCAAAGTGC T C AC006059.2 Ensembl:ENSG00000280571 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1480265740 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15520 43797 RMVar_ID_43797 Human_SNP_ID_130887249 A-to-I Human chr3 - 42783859 42783859 42783859 GTTGGCCAGGCTGATCTTGAATTCCTGACCTCAGGTTATCCACCTGCCTCGGCCTCCCAAAGTGC GTTGGCCAGGCTGATCTTGAATTCCTGACCTCCGGTTATCCACCTGCCTCGGCCTCCCAAAGTGC T G AC006059.2 Ensembl:ENSG00000280571 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1480265740 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15520 43798 RMVar_ID_43798 Human_SNP_ID_130888580 A-to-I Human chr3 - 42789499 42789498 42789499 ATTTATTTTTTATTAAAATTTTTTTTTTTTGTAGACACAGGTCTCACTCTGTTGCCCATGCTGGT ATTTATTTTTTATTAAAATTTTTTTTTTTTGT_GACACAGGTCTCACTCTGTTGCCCATGCTGGT CT C HIGD1A,AC006059.2,AC099329.1 Ensembl:ENSG00000181061,Ensembl:ENSG00000280571,Ensembl:ENSG00000235288 Protein coding,Protein coding,lincRNA intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1198584088 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_14821958 RMVar_hsa_circ_61268 43799 RMVar_ID_43799 Human_SNP_ID_130918276 A-to-I Human chr3 + 42917905 42917905 42917905 AAGGTGGGCAGATCACCTGAGATTGGGAGTTCAAGACCAGCCTGACCAACATAGAGAGACCCCGT AAGGTGGGCAGATCACCTGAGATTGGGAGTTCGAGACCAGCCTGACCAACATAGAGAGACCCCGT A G KRBOX1,AC092042.3,ZNF662 Ensembl:ENSG00000240747,Ensembl:ENSG00000273291,Ensembl:ENSG00000182983 Protein coding,Protein coding,Protein coding intron,intron,3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1470510282 Functional Loss SNV dbSNP153 33..33 33 - - - 43800 RMVar_ID_43800 Human_SNP_ID_131112595 A-to-I Human chr3 + 43733221 43733221 43733221 ACCAGGAGACTGGGATCCCTGGGGGCTGTCTTAGAGCTTACTCACTACCACACTCATTCATAATA ACCAGGAGACTGGGATCCCTGGGGGCTGTCTTGGAGCTTACTCACTACCACACTCATTCATAATA A G ABHD5 Ensembl:ENSG00000011198 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973290232 Functional Loss SNV dbSNP153 33..33 33 - - - 43801 RMVar_ID_43801 Human_SNP_ID_131255688 A-to-I Human chr3 + 44344101 44344101 44344101 TGGAGTGCAGTGGTGCAATCTCAGCTCACTGCAAACTCCACCTCCCAGGCTCAAGGCCTCAGCCT TGGAGTGCAGTGGTGCAATCTCAGCTCACTGCGAACTCCACCTCCCAGGCTCAAGGCCTCAGCCT A G TCAIM Ensembl:ENSG00000179152 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1303467331 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_217301,RMVar_hsa_circ_88780,RMVar_hsa_circ_217302 43802 RMVar_ID_43802 Human_SNP_ID_131259342 A-to-I Human chr3 + 44359199 44359199 44359199 CTTGAGCCCAGGAATTCAAGCCTGGGCAACATAGTGAGTCCTCATCTCCTAAATTTAAAAAACAA CTTGAGCCCAGGAATTCAAGCCTGGGCAACATGGTGAGTCCTCATCTCCTAAATTTAAAAAACAA A G TCAIM Ensembl:ENSG00000179152 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1250535901 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_602179 RMVar_hsa_circ_94438,RMVar_hsa_circ_27656,RMVar_hsa_circ_217301,RMVar_hsa_circ_88780,RMVar_hsa_circ_285023,RMVar_hsa_circ_296563,RMVar_hsa_circ_362091,RMVar_hsa_circ_217302,RMVar_hsa_circ_303038,RMVar_hsa_circ_294956,RMVar_hsa_circ_280775,RMVar_hsa_circ_217304,RMVar_hsa_circ_217305,RMVar_hsa_circ_313964,RMVar_hsa_circ_217303,RMVar_hsa_circ_285858,RMVar_hsa_circ_217307,RMVar_hsa_circ_217308,RMVar_hsa_circ_217306,RMVar_hsa_circ_217309 43803 RMVar_ID_43803 Human_SNP_ID_131261427 A-to-I Human chr3 + 44368765 44368765 44368765 AAATGAAGAGCCTGGCACTGTGGCTTATGCCGATAATCCCAGCATTTGGGGAGGCCGAGGTGGGA AAATGAAGAGCCTGGCACTGTGGCTTATGCCGGTAATCCCAGCATTTGGGGAGGCCGAGGTGGGA A G TCAIM Ensembl:ENSG00000179152 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs913941606 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27656,RMVar_hsa_circ_296563,RMVar_hsa_circ_362091,RMVar_hsa_circ_303038,RMVar_hsa_circ_217304,RMVar_hsa_circ_217305,RMVar_hsa_circ_313964,RMVar_hsa_circ_217306,RMVar_hsa_circ_217313,RMVar_hsa_circ_285136,RMVar_hsa_circ_340669,RMVar_hsa_circ_363312,RMVar_hsa_circ_217312,RMVar_hsa_circ_273610,RMVar_hsa_circ_217311,RMVar_hsa_circ_217315,RMVar_hsa_circ_294452,RMVar_hsa_circ_341370,RMVar_hsa_circ_292534,RMVar_hsa_circ_217314,RMVar_hsa_circ_217317,RMVar_hsa_circ_282096,RMVar_hsa_circ_298646,RMVar_hsa_circ_64084,RMVar_hsa_circ_217316 43804 RMVar_ID_43804 Human_SNP_ID_131261459 A-to-I Human chr3 + 44368968 44368968 44368968 TCCCTTGAGCACAGGAGTTTGAGGCTGCGGTGAACTATGATTGTGCCACTGCACTCCAGCCTGGG TCCCTTGAGCACAGGAGTTTGAGGCTGCGGTGGACTATGATTGTGCCACTGCACTCCAGCCTGGG A G TCAIM Ensembl:ENSG00000179152 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1445209080 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27656,RMVar_hsa_circ_296563,RMVar_hsa_circ_362091,RMVar_hsa_circ_303038,RMVar_hsa_circ_217304,RMVar_hsa_circ_217305,RMVar_hsa_circ_313964,RMVar_hsa_circ_217306,RMVar_hsa_circ_217313,RMVar_hsa_circ_285136,RMVar_hsa_circ_340669,RMVar_hsa_circ_363312,RMVar_hsa_circ_217312,RMVar_hsa_circ_273610,RMVar_hsa_circ_217311,RMVar_hsa_circ_217315,RMVar_hsa_circ_294452,RMVar_hsa_circ_341370,RMVar_hsa_circ_292534,RMVar_hsa_circ_217314,RMVar_hsa_circ_217317,RMVar_hsa_circ_282096,RMVar_hsa_circ_298646,RMVar_hsa_circ_64084,RMVar_hsa_circ_217316 43805 RMVar_ID_43805 Human_SNP_ID_131261460 A-to-I Human chr3 + 44368972 44368972 44368972 TTGAGCACAGGAGTTTGAGGCTGCGGTGAACTATGATTGTGCCACTGCACTCCAGCCTGGGTGAC TTGAGCACAGGAGTTTGAGGCTGCGGTGAACTGTGATTGTGCCACTGCACTCCAGCCTGGGTGAC A G TCAIM Ensembl:ENSG00000179152 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1261031367 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27656,RMVar_hsa_circ_296563,RMVar_hsa_circ_362091,RMVar_hsa_circ_303038,RMVar_hsa_circ_217304,RMVar_hsa_circ_217305,RMVar_hsa_circ_313964,RMVar_hsa_circ_217306,RMVar_hsa_circ_217313,RMVar_hsa_circ_285136,RMVar_hsa_circ_340669,RMVar_hsa_circ_363312,RMVar_hsa_circ_217312,RMVar_hsa_circ_273610,RMVar_hsa_circ_217311,RMVar_hsa_circ_217315,RMVar_hsa_circ_294452,RMVar_hsa_circ_341370,RMVar_hsa_circ_292534,RMVar_hsa_circ_217314,RMVar_hsa_circ_217317,RMVar_hsa_circ_282096,RMVar_hsa_circ_298646,RMVar_hsa_circ_64084,RMVar_hsa_circ_217316 43806 RMVar_ID_43806 Human_SNP_ID_131262024 A-to-I Human chr3 + 44371272 44371272 44371272 TAGAGACAAGGTCTCACTATGTTGTGCAGGCTAGTCTCAAACTCCTGAGCTCAAGCGATCCCCCT TAGAGACAAGGTCTCACTATGTTGTGCAGGCTGGTCTCAAACTCCTGAGCTCAAGCGATCCCCCT A G TCAIM Ensembl:ENSG00000179152 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs905709372 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27656,RMVar_hsa_circ_296563,RMVar_hsa_circ_362091,RMVar_hsa_circ_303038,RMVar_hsa_circ_217304,RMVar_hsa_circ_217305,RMVar_hsa_circ_313964,RMVar_hsa_circ_217306,RMVar_hsa_circ_217313,RMVar_hsa_circ_285136,RMVar_hsa_circ_340669,RMVar_hsa_circ_363312,RMVar_hsa_circ_217312,RMVar_hsa_circ_273610,RMVar_hsa_circ_217311,RMVar_hsa_circ_217315,RMVar_hsa_circ_294452,RMVar_hsa_circ_341370,RMVar_hsa_circ_292534,RMVar_hsa_circ_217314,RMVar_hsa_circ_217317,RMVar_hsa_circ_282096,RMVar_hsa_circ_298646,RMVar_hsa_circ_64084,RMVar_hsa_circ_217316 43807 RMVar_ID_43807 Human_SNP_ID_131262478 A-to-I Human chr3 + 44372658 44372658 44372658 CTCAGTCGCCCAGGCTGGAGTGCAGTGGTGCTATCTTGGCTCACTGCAAGCTCCGCCTCCCGGGT CTCAGTCGCCCAGGCTGGAGTGCAGTGGTGCTGTCTTGGCTCACTGCAAGCTCCGCCTCCCGGGT A G TCAIM Ensembl:ENSG00000179152 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223130041 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27656,RMVar_hsa_circ_296563,RMVar_hsa_circ_362091,RMVar_hsa_circ_303038,RMVar_hsa_circ_217304,RMVar_hsa_circ_217305,RMVar_hsa_circ_313964,RMVar_hsa_circ_217306,RMVar_hsa_circ_217313,RMVar_hsa_circ_285136,RMVar_hsa_circ_340669,RMVar_hsa_circ_363312,RMVar_hsa_circ_217312,RMVar_hsa_circ_273610,RMVar_hsa_circ_217311,RMVar_hsa_circ_217315,RMVar_hsa_circ_294452,RMVar_hsa_circ_341370,RMVar_hsa_circ_292534,RMVar_hsa_circ_217314,RMVar_hsa_circ_217317,RMVar_hsa_circ_282096,RMVar_hsa_circ_298646,RMVar_hsa_circ_64084,RMVar_hsa_circ_217316 43808 RMVar_ID_43808 Human_SNP_ID_131262539 A-to-I Human chr3 + 44372833 44372833 44372833 AGCCAGGATGGTCTTGATCTCCTGACCTCATGATCCACCCGTCTTGGCCTCCCAAAGCACTGGGA AGCCAGGATGGTCTTGATCTCCTGACCTCATGGTCCACCCGTCTTGGCCTCCCAAAGCACTGGGA A G TCAIM Ensembl:ENSG00000179152 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs965062884 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27656,RMVar_hsa_circ_296563,RMVar_hsa_circ_362091,RMVar_hsa_circ_303038,RMVar_hsa_circ_217304,RMVar_hsa_circ_217305,RMVar_hsa_circ_313964,RMVar_hsa_circ_217306,RMVar_hsa_circ_217313,RMVar_hsa_circ_285136,RMVar_hsa_circ_340669,RMVar_hsa_circ_363312,RMVar_hsa_circ_217312,RMVar_hsa_circ_273610,RMVar_hsa_circ_217311,RMVar_hsa_circ_217315,RMVar_hsa_circ_294452,RMVar_hsa_circ_341370,RMVar_hsa_circ_292534,RMVar_hsa_circ_217314,RMVar_hsa_circ_217317,RMVar_hsa_circ_282096,RMVar_hsa_circ_298646,RMVar_hsa_circ_64084,RMVar_hsa_circ_217316 43809 RMVar_ID_43809 Human_SNP_ID_131262540 A-to-I Human chr3 + 44372833 44372833 44372833 AGCCAGGATGGTCTTGATCTCCTGACCTCATGATCCACCCGTCTTGGCCTCCCAAAGCACTGGGA AGCCAGGATGGTCTTGATCTCCTGACCTCATGTTCCACCCGTCTTGGCCTCCCAAAGCACTGGGA A T TCAIM Ensembl:ENSG00000179152 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs965062884 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27656,RMVar_hsa_circ_296563,RMVar_hsa_circ_362091,RMVar_hsa_circ_303038,RMVar_hsa_circ_217304,RMVar_hsa_circ_217305,RMVar_hsa_circ_313964,RMVar_hsa_circ_217306,RMVar_hsa_circ_217313,RMVar_hsa_circ_285136,RMVar_hsa_circ_340669,RMVar_hsa_circ_363312,RMVar_hsa_circ_217312,RMVar_hsa_circ_273610,RMVar_hsa_circ_217311,RMVar_hsa_circ_217315,RMVar_hsa_circ_294452,RMVar_hsa_circ_341370,RMVar_hsa_circ_292534,RMVar_hsa_circ_217314,RMVar_hsa_circ_217317,RMVar_hsa_circ_282096,RMVar_hsa_circ_298646,RMVar_hsa_circ_64084,RMVar_hsa_circ_217316 43810 RMVar_ID_43810 Human_SNP_ID_131262542 A-to-I Human chr3 + 44372837 44372837 44372837 AGGATGGTCTTGATCTCCTGACCTCATGATCCACCCGTCTTGGCCTCCCAAAGCACTGGGATTAC AGGATGGTCTTGATCTCCTGACCTCATGATCCGCCCGTCTTGGCCTCCCAAAGCACTGGGATTAC A G TCAIM Ensembl:ENSG00000179152 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1163493184 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27656,RMVar_hsa_circ_296563,RMVar_hsa_circ_362091,RMVar_hsa_circ_303038,RMVar_hsa_circ_217304,RMVar_hsa_circ_217305,RMVar_hsa_circ_313964,RMVar_hsa_circ_217306,RMVar_hsa_circ_217313,RMVar_hsa_circ_285136,RMVar_hsa_circ_340669,RMVar_hsa_circ_363312,RMVar_hsa_circ_217312,RMVar_hsa_circ_273610,RMVar_hsa_circ_217311,RMVar_hsa_circ_217315,RMVar_hsa_circ_294452,RMVar_hsa_circ_341370,RMVar_hsa_circ_292534,RMVar_hsa_circ_217314,RMVar_hsa_circ_217317,RMVar_hsa_circ_282096,RMVar_hsa_circ_298646,RMVar_hsa_circ_64084,RMVar_hsa_circ_217316 43811 RMVar_ID_43811 Human_SNP_ID_131262550 A-to-I Human chr3 + 44372859 44372859 44372859 CTCATGATCCACCCGTCTTGGCCTCCCAAAGCACTGGGATTACAGGTGTGAGCCACTGCACCCGG CTCATGATCCACCCGTCTTGGCCTCCCAAAGCGCTGGGATTACAGGTGTGAGCCACTGCACCCGG A G TCAIM Ensembl:ENSG00000179152 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1489883385 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27656,RMVar_hsa_circ_296563,RMVar_hsa_circ_362091,RMVar_hsa_circ_303038,RMVar_hsa_circ_217304,RMVar_hsa_circ_217305,RMVar_hsa_circ_313964,RMVar_hsa_circ_217306,RMVar_hsa_circ_217313,RMVar_hsa_circ_285136,RMVar_hsa_circ_340669,RMVar_hsa_circ_363312,RMVar_hsa_circ_217312,RMVar_hsa_circ_273610,RMVar_hsa_circ_217311,RMVar_hsa_circ_217315,RMVar_hsa_circ_294452,RMVar_hsa_circ_341370,RMVar_hsa_circ_292534,RMVar_hsa_circ_217314,RMVar_hsa_circ_217317,RMVar_hsa_circ_282096,RMVar_hsa_circ_298646,RMVar_hsa_circ_64084,RMVar_hsa_circ_217316 43812 RMVar_ID_43812 Human_SNP_ID_131262672 A-to-I Human chr3 + 44373456 44373456 44373456 GGGAAGCTGAGGTGGGCAGATCACTTGATGTCAAGATGGTGGCCAACATGGTGAAACCCCATCTC GGGAAGCTGAGGTGGGCAGATCACTTGATGTCGAGATGGTGGCCAACATGGTGAAACCCCATCTC A G TCAIM Ensembl:ENSG00000179152 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1057060918 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27656,RMVar_hsa_circ_296563,RMVar_hsa_circ_362091,RMVar_hsa_circ_303038,RMVar_hsa_circ_217304,RMVar_hsa_circ_217305,RMVar_hsa_circ_313964,RMVar_hsa_circ_217306,RMVar_hsa_circ_217313,RMVar_hsa_circ_285136,RMVar_hsa_circ_340669,RMVar_hsa_circ_363312,RMVar_hsa_circ_217312,RMVar_hsa_circ_273610,RMVar_hsa_circ_217311,RMVar_hsa_circ_217315,RMVar_hsa_circ_294452,RMVar_hsa_circ_341370,RMVar_hsa_circ_292534,RMVar_hsa_circ_217314,RMVar_hsa_circ_217317,RMVar_hsa_circ_282096,RMVar_hsa_circ_298646,RMVar_hsa_circ_64084,RMVar_hsa_circ_217316 43813 RMVar_ID_43813 Human_SNP_ID_131262722 A-to-I Human chr3 + 44373614 44373614 44373614 AGGCAGAGATTGCAGTGAACCAAGATCGTGCCACTGCACTCTAGCGTGGGTGACAGAGTGAGACT AGGCAGAGATTGCAGTGAACCAAGATCGTGCCCCTGCACTCTAGCGTGGGTGACAGAGTGAGACT A C TCAIM Ensembl:ENSG00000179152 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs891082730 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25737211 RMVar_hsa_circ_27656,RMVar_hsa_circ_296563,RMVar_hsa_circ_362091,RMVar_hsa_circ_303038,RMVar_hsa_circ_217304,RMVar_hsa_circ_217305,RMVar_hsa_circ_313964,RMVar_hsa_circ_217306,RMVar_hsa_circ_217313,RMVar_hsa_circ_285136,RMVar_hsa_circ_340669,RMVar_hsa_circ_363312,RMVar_hsa_circ_217312,RMVar_hsa_circ_273610,RMVar_hsa_circ_217311,RMVar_hsa_circ_217315,RMVar_hsa_circ_294452,RMVar_hsa_circ_341370,RMVar_hsa_circ_292534,RMVar_hsa_circ_217314,RMVar_hsa_circ_217317,RMVar_hsa_circ_282096,RMVar_hsa_circ_298646,RMVar_hsa_circ_64084,RMVar_hsa_circ_217316 43814 RMVar_ID_43814 Human_SNP_ID_131262729 A-to-I Human chr3 + 44373636 44373636 44373636 AGATCGTGCCACTGCACTCTAGCGTGGGTGACAGAGTGAGACTCTGTCTGAAAAAAAGAGAAAAG AGATCGTGCCACTGCACTCTAGCGTGGGTGACGGAGTGAGACTCTGTCTGAAAAAAAGAGAAAAG A G TCAIM Ensembl:ENSG00000179152 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1036874317 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27656,RMVar_hsa_circ_296563,RMVar_hsa_circ_362091,RMVar_hsa_circ_303038,RMVar_hsa_circ_217304,RMVar_hsa_circ_217305,RMVar_hsa_circ_313964,RMVar_hsa_circ_217306,RMVar_hsa_circ_217313,RMVar_hsa_circ_285136,RMVar_hsa_circ_340669,RMVar_hsa_circ_363312,RMVar_hsa_circ_217312,RMVar_hsa_circ_273610,RMVar_hsa_circ_217311,RMVar_hsa_circ_217315,RMVar_hsa_circ_294452,RMVar_hsa_circ_341370,RMVar_hsa_circ_292534,RMVar_hsa_circ_217314,RMVar_hsa_circ_217317,RMVar_hsa_circ_282096,RMVar_hsa_circ_298646,RMVar_hsa_circ_64084,RMVar_hsa_circ_217316 43815 RMVar_ID_43815 Human_SNP_ID_131262921 A-to-I Human chr3 + 44374498 44374498 44374498 GCTTTTGGTGCCAGGTGCAGTGGCTTCTAACTATAATCCCAGCACTTTGGGAGGCCAAGGCGGGA GCTTTTGGTGCCAGGTGCAGTGGCTTCTAACTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGA A G TCAIM Ensembl:ENSG00000179152 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1559572464 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27656,RMVar_hsa_circ_296563,RMVar_hsa_circ_362091,RMVar_hsa_circ_303038,RMVar_hsa_circ_217304,RMVar_hsa_circ_217305,RMVar_hsa_circ_313964,RMVar_hsa_circ_217306,RMVar_hsa_circ_217313,RMVar_hsa_circ_285136,RMVar_hsa_circ_340669,RMVar_hsa_circ_363312,RMVar_hsa_circ_217312,RMVar_hsa_circ_273610,RMVar_hsa_circ_217311,RMVar_hsa_circ_217315,RMVar_hsa_circ_294452,RMVar_hsa_circ_341370,RMVar_hsa_circ_292534,RMVar_hsa_circ_217314,RMVar_hsa_circ_217317,RMVar_hsa_circ_282096,RMVar_hsa_circ_298646,RMVar_hsa_circ_64084,RMVar_hsa_circ_217316 43816 RMVar_ID_43816 Human_SNP_ID_131276680 A-to-I Human chr3 - 44433266 44433266 44433266 CTACTAAAAATACAAAAGTAGCCAGGCGTGGTAGCGGGCACCTGTAAATCCCAGCTACTGGGGAG CTACTAAAAATACAAAAGTAGCCAGGCGTGGTGGCGGGCACCTGTAAATCCCAGCTACTGGGGAG T C C3orf86,ZNF445 Ensembl:ENSG00000225873,Ensembl:ENSG00000185219 Pseudogene,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1205919785 Functional Loss SNV dbSNP153 33..33 33 - - - 43817 RMVar_ID_43817 Human_SNP_ID_131278033 A-to-I Human chr3 - 44438220 44438220 44438220 AGGAGGTGGAAGTTGCAGTGAGCCGAGATCGCACAACTGCACTCCAGCCTGGGCGACAGAGTGAA AGGAGGTGGAAGTTGCAGTGAGCCGAGATCGCGCAACTGCACTCCAGCCTGGGCGACAGAGTGAA T C C3orf86,ZNF445 Ensembl:ENSG00000225873,Ensembl:ENSG00000185219 Pseudogene,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432425460 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17405696,Human_RBP_ID_18409565,Human_RBP_ID_25737235 43818 RMVar_ID_43818 Human_SNP_ID_131278302 A-to-I Human chr3 - 44439128 44439128 44439128 TTTTTGTATTTTTGTAGAGACAAGGTTTGGCCATGTTGCCCAAGCTGGTCTTGAACTCCTGACCT TTTTTGTATTTTTGTAGAGACAAGGTTTGGCCGTGTTGCCCAAGCTGGTCTTGAACTCCTGACCT T C C3orf86,ZNF445 Ensembl:ENSG00000225873,Ensembl:ENSG00000185219 Pseudogene,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1461645295 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8264780,Human_RBP_ID_14824922 43819 RMVar_ID_43819 Human_SNP_ID_131284932 A-to-I Human chr3 - 44464984 44464984 44464984 TGGCTCACTGCAACCTCCGCCTGCCGGGTTCAAGCAATTCTGCTGCCTCAGCCTACCGAGTAGCT TGGCTCACTGCAACCTCCGCCTGCCGGGTTCAGGCAATTCTGCTGCCTCAGCCTACCGAGTAGCT T C ZNF445 Ensembl:ENSG00000185219 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs911188562 Functional Loss SNV dbSNP153 33..33 33 - - - 43820 RMVar_ID_43820 Human_SNP_ID_131289695 A-to-I Human chr3 + 44483930 44483930 44483930 AATCACACAGCTCACTGCAGCCTTGACCTCCCAGGCTCAAGCGATCCTCCCACCTCAGCCCCTGA AATCACACAGCTCACTGCAGCCTTGACCTCCCTGGCTCAAGCGATCCTCCCACCTCAGCCCCTGA A T lnc-ZKSCAN7-4,lnc-ZKSCAN7-4:2,lnc-ZKSCAN7-4:3 RNACentral:URS0000D5DFB9,RNACentral:URS0000D5BB96,RNACentral:URS0000D57E45 lincRNA,lincRNA,lincRNA exon,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1242617229 Functional Loss SNV dbSNP153 33..33 33 - - - 43821 RMVar_ID_43821 Human_SNP_ID_131289723 A-to-I Human chr3 + 44484026 44484026 44484026 CCCGGCTAATTTTTTTGTATTTTTGTAGACACAAGGTTTTGCTATATTGCCCTGGCTGGTCTCAA CCCGGCTAATTTTTTTGTATTTTTGTAGACACGAGGTTTTGCTATATTGCCCTGGCTGGTCTCAA A G lnc-ZKSCAN7-4,lnc-ZKSCAN7-4:2,lnc-ZKSCAN7-4:3 RNACentral:URS0000D5DFB9,RNACentral:URS0000D5BB96,RNACentral:URS0000D57E45 lincRNA,lincRNA,lincRNA exon,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs915458797 Functional Loss SNV dbSNP153 33..33 33 - - - 43822 RMVar_ID_43822 Human_SNP_ID_131291840 A-to-I Human chr3 - 44493766 44493766 44493766 CTGTAATCCCAGCTACACGGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGAGAGACAGAGGTT CTGTAATCCCAGCTACACGGGGAGGCTGAGGCCGGAGAATCGCTTGAACCCGAGAGACAGAGGTT T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1004966906 Functional Loss SNV dbSNP153 33..33 33 - - - 43823 RMVar_ID_43823 Human_SNP_ID_131291928 A-to-I Human chr3 - 44494207 44494207 44494207 CCAAGTCTTTTAAGGGCGTTAGTGAGAGTGACAGCCCCATTCTCATGACCTACTCCAATCCTAGT CCAAGTCTTTTAAGGGCGTTAGTGAGAGTGACGGCCCCATTCTCATGACCTACTCCAATCCTAGT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs375811956 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14825643 43824 RMVar_ID_43824 Human_SNP_ID_131292335 A-to-I Human chr3 - 44496281 44496281 44496281 CTGTAATCCCAGCTATTCAGGAGTCTGAGGCAAGAGAATCACTTGAACCTGGAGGGCAGAGATTG CTGTAATCCCAGCTATTCAGGAGTCTGAGGCAGGAGAATCACTTGAACCTGGAGGGCAGAGATTG T C ZNF852 Ensembl:ENSG00000178917 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1376220626 Functional Loss SNV dbSNP153 33..33 33 - - - 43825 RMVar_ID_43825 Human_SNP_ID_131292777 A-to-I Human chr3 - 44498229 44498229 44498229 TTTTGTATTTTTAGTAGAGATGGGGTTTCTCTATGTTGGTCAGGCTGGTCTTGAACTCCCAATCT TTTTGTATTTTTAGTAGAGATGGGGTTTCTCTGTGTTGGTCAGGCTGGTCTTGAACTCCCAATCT T C ZNF852 Ensembl:ENSG00000178917 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs901386866 Functional Loss SNV dbSNP153 33..33 33 - - - 43826 RMVar_ID_43826 Human_SNP_ID_131292814 A-to-I Human chr3 - 44498371 44498371 44498371 TCTTGTTGCCCAGGCTAGAGTGCAATGGTGCAATCTTGGCTCACCACAACCTCTGCTTCTCGGGT TCTTGTTGCCCAGGCTAGAGTGCAATGGTGCAGTCTTGGCTCACCACAACCTCTGCTTCTCGGGT T C ZNF852 Ensembl:ENSG00000178917 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs538476353 Functional Loss SNV dbSNP153 33..33 33 - - - 43827 RMVar_ID_43827 Human_SNP_ID_131292816 A-to-I Human chr3 - 44498379 44498379 44498379 AGTCTCCCTCTTGTTGCCCAGGCTAGAGTGCAATGGTGCAATCTTGGCTCACCACAACCTCTGCT AGTCTCCCTCTTGTTGCCCAGGCTAGAGTGCAGTGGTGCAATCTTGGCTCACCACAACCTCTGCT T C ZNF852 Ensembl:ENSG00000178917 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1034805411 Functional Loss SNV dbSNP153 33..33 33 - - - 43828 RMVar_ID_43828 Human_SNP_ID_131294984 A-to-I Human chr3 - 44506815 44506815 44506815 CCAGCTACTTGGAAGGCTGAGGCTGGAGAATCACTTGAATCCAGGAGACGGAGGTTGCAGTGAGC CCAGCTACTTGGAAGGCTGAGGCTGGAGAATCGCTTGAATCCAGGAGACGGAGGTTGCAGTGAGC T C ZNF852 Ensembl:ENSG00000178917 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs777410370 Functional Loss SNV dbSNP153 33..33 33 - - - 43829 RMVar_ID_43829 Human_SNP_ID_131294989 A-to-I Human chr3 - 44506851 44506851 44506851 AAAATTGGCTGGGCATGGTGGTGCATGCCTGTAATCCCAGCTACTTGGAAGGCTGAGGCTGGAGA AAAATTGGCTGGGCATGGTGGTGCATGCCTGTGATCCCAGCTACTTGGAAGGCTGAGGCTGGAGA T C ZNF852 Ensembl:ENSG00000178917 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025429759 Functional Loss SNV dbSNP153 33..33 33 - - - 43830 RMVar_ID_43830 Human_SNP_ID_131295285 A-to-I Human chr3 - 44508024 44508024 44508024 CACCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGACGTGAGCCACCGCGCCTGGCCAGTCTCA CACCCGCCTTGGCCTCCCAAAGTGCTGGGATTGCAGACGTGAGCCACCGCGCCTGGCCAGTCTCA T C ZNF852 Ensembl:ENSG00000178917 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1283854280 Functional Loss SNV dbSNP153 33..33 33 - - - 43831 RMVar_ID_43831 Human_SNP_ID_131312024 A-to-I Human chr3 - 44578248 44578248 44578248 GAGATTAGCTCCCTCAAGGATGAGCTGCAGACAGCACTGTGGGACAAGAAGTACGCAAGTGACAC GAGATTAGCTCCCTCAAGGATGAGCTGCAGACGGCACTGTGGGACAAGAAGTACGCAAGTGACAC T C ZKSCAN7-AS1 Ensembl:ENSG00000236869 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1191983101 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5602442 43832 RMVar_ID_43832 Human_SNP_ID_131312047 A-to-I Human chr3 - 44578309 44578309 44578309 TGCCTATGAACTAGAAGTCTTATTGCGGATATAGGAATCGGAAATACAGTACCTGAAACAGGAGA TGCCTATGAACTAGAAGTCTTATTGCGGATATGGGAATCGGAAATACAGTACCTGAAACAGGAGA T C ZKSCAN7-AS1 Ensembl:ENSG00000236869 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs751292526 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5604385 43833 RMVar_ID_43833 Human_SNP_ID_131312051 A-to-I Human chr3 - 44578313 44578313 44578313 AGGATGCCTATGAACTAGAAGTCTTATTGCGGATATAGGAATCGGAAATACAGTACCTGAAACAG AGGATGCCTATGAACTAGAAGTCTTATTGCGGGTATAGGAATCGGAAATACAGTACCTGAAACAG T C ZKSCAN7-AS1 Ensembl:ENSG00000236869 lincRNA intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1488909418 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5604385 43834 RMVar_ID_43834 Human_SNP_ID_131312058 A-to-I Human chr3 - 44578326 44578326 44578326 CTTGCACAGGGCAAGGATGCCTATGAACTAGAAGTCTTATTGCGGATATAGGAATCGGAAATACA CTTGCACAGGGCAAGGATGCCTATGAACTAGAGGTCTTATTGCGGATATAGGAATCGGAAATACA T C ZKSCAN7-AS1 Ensembl:ENSG00000236869 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1310036647 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5604385 43835 RMVar_ID_43835 Human_SNP_ID_131312226 A-to-I Human chr3 - 44578862 44578862 44578862 CCCGTGAGGGCTACATGCTGCAGGCCACGTGCAAGTGAGGGTTTGCAGCAATGGAAGAAACGCAC CCCGTGAGGGCTACATGCTGCAGGCCACGTGCGAGTGAGGGTTTGCAGCAATGGAAGAAACGCAC T C ZKSCAN7-AS1 Ensembl:ENSG00000236869 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878938276 Functional Loss SNV dbSNP153 33..33 33 - - - 43836 RMVar_ID_43836 Human_SNP_ID_131312230 A-to-I Human chr3 - 44578880 44578880 44578880 TGGGCCGGGAGCAGAGCGCCCGTGAGGGCTACATGCTGCAGGCCACGTGCAAGTGAGGGTTTGCA TGGGCCGGGAGCAGAGCGCCCGTGAGGGCTACGTGCTGCAGGCCACGTGCAAGTGAGGGTTTGCA T C ZKSCAN7-AS1 Ensembl:ENSG00000236869 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs867633620 Functional Loss SNV dbSNP153 33..33 33 - - - 43837 RMVar_ID_43837 Human_SNP_ID_131351726 A-to-I Human chr3 - 44749132 44749132 44749132 CACCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCAGGAGCCACCGCGCCTGGGCCTTTTTT CACCTGCCTCGGCCTCCCAAAGTGCTGGGATTGCAGGCAGGAGCCACCGCGCCTGGGCCTTTTTT T C KIAA1143 Ensembl:ENSG00000163807 Protein coding intron GSE38233;GSE107867 cultured B-cells;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 24183664,30559470 RNA-Seq:(High) rs1424657100 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_602349 RMVar_hsa_circ_82352,RMVar_hsa_circ_109506,RMVar_hsa_circ_106545,RMVar_hsa_circ_217337,RMVar_hsa_circ_217338,RMVar_hsa_circ_217339 43838 RMVar_ID_43838 Human_SNP_ID_131351728 A-to-I Human chr3 - 44749144 44749144 44749144 GACCTCATGATCCACCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCAGGAGCCACCGCGCC GACCTCATGATCCACCTGCCTCGGCCTCCCAAGGTGCTGGGATTACAGGCAGGAGCCACCGCGCC T C KIAA1143 Ensembl:ENSG00000163807 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs11546548 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_602349 RMVar_hsa_circ_82352,RMVar_hsa_circ_109506,RMVar_hsa_circ_106545,RMVar_hsa_circ_217337,RMVar_hsa_circ_217338,RMVar_hsa_circ_217339 43839 RMVar_ID_43839 Human_SNP_ID_131351764 A-to-I Human chr3 - 44749281 44749281 44749281 GGGTTCACACCATTCTCTTGCCTCAGCCTCCCAAGTATCTGGGACTACAGTCGCCCGCCACCACG GGGTTCACACCATTCTCTTGCCTCAGCCTCCCGAGTATCTGGGACTACAGTCGCCCGCCACCACG T C KIAA1143 Ensembl:ENSG00000163807 Protein coding intron GSE47997;GSE38233;GSE112787;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;cultured B-cells;293 Flip-In T-REx cells,empty vector;ASD brains,temporal_cortex;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,24183664,29967493,30559470,31158229,31158229 RNA-Seq:(High) rs1182622866 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82352,RMVar_hsa_circ_109506,RMVar_hsa_circ_106545,RMVar_hsa_circ_217337,RMVar_hsa_circ_217338,RMVar_hsa_circ_217339 43840 RMVar_ID_43840 Human_SNP_ID_131351766 A-to-I Human chr3 - 44749289 44749289 44749289 CGCCTCCTGGGTTCACACCATTCTCTTGCCTCAGCCTCCCAAGTATCTGGGACTACAGTCGCCCG CGCCTCCTGGGTTCACACCATTCTCTTGCCTCGGCCTCCCAAGTATCTGGGACTACAGTCGCCCG T C KIAA1143 Ensembl:ENSG00000163807 Protein coding intron GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831 esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line - 29796672,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs1473820386 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82352,RMVar_hsa_circ_109506,RMVar_hsa_circ_106545,RMVar_hsa_circ_217337,RMVar_hsa_circ_217338,RMVar_hsa_circ_217339 43841 RMVar_ID_43841 Human_SNP_ID_131351786 A-to-I Human chr3 - 44749367 44749367 44749367 TTTGTTTTTTTGAGACAGAGTCTCGCTCTGTCACCCAGGCTGGAGTGCAGTGGCGCGATCTCAGC TTTGTTTTTTTGAGACAGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCGATCTCAGC T C KIAA1143 Ensembl:ENSG00000163807 Protein coding intron GSE38233;GSE112787;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;293 Flip-In T-REx cells,empty vector;Bronchiolar epithelium,BEP2D cell line - 24183664,29967493,31158229 RNA-Seq:(High) rs1165766029 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82352,RMVar_hsa_circ_109506,RMVar_hsa_circ_106545,RMVar_hsa_circ_217337,RMVar_hsa_circ_217338,RMVar_hsa_circ_217339 43842 RMVar_ID_43842 Human_SNP_ID_131351791 A-to-I Human chr3 - 44749387 44749387 44749387 CTTTTTTAAGTTTGTTTTGTTTTGTTTTTTTGAGACAGAGTCTCGCTCTGTCACCCAGGCTGGAG CTTTTTTAAGTTTGTTTTGTTTTGTTTTTTTGGGACAGAGTCTCGCTCTGTCACCCAGGCTGGAG T C KIAA1143 Ensembl:ENSG00000163807 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1141637 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7197778 RMVar_hsa_circ_82352,RMVar_hsa_circ_109506,RMVar_hsa_circ_106545,RMVar_hsa_circ_217337,RMVar_hsa_circ_217338,RMVar_hsa_circ_217339 43843 RMVar_ID_43843 Human_SNP_ID_131351797 A-to-I Human chr3 - 44749411 44749406 44749412 CTTACAAATTTGGTGCCACATTATCTTTTTTAAGTTTGTTTTGTTTTGTTTTTTTGAGACAGAGT CTTACAAATTTGGTGCCACATTATCTTTTTT______GTTTTGTTTTGTTTTTTTGAGACAGAGT CAAACTT C KIAA1143 Ensembl:ENSG00000163807 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223405593 Functional Loss DEL dbSNP153 32..37 33 - - - Human_RBP_ID_7197778,Human_RBP_ID_8209687 RMVar_hsa_circ_82352,RMVar_hsa_circ_109506,RMVar_hsa_circ_106545,RMVar_hsa_circ_217337,RMVar_hsa_circ_217338,RMVar_hsa_circ_217339 43844 RMVar_ID_43844 Human_SNP_ID_131351822 A-to-I Human chr3 - 44749570 44749570 44749570 GGGAGGGGAAGCACTTTAAAGTCTGAGCCTTTAGAGGTGATTCCTCAAGACCCTGCTTAATCCTA GGGAGGGGAAGCACTTTAAAGTCTGAGCCTTTCGAGGTGATTCCTCAAGACCCTGCTTAATCCTA T G KIAA1143 Ensembl:ENSG00000163807 Protein coding intron GSE38233;GSE107867;GSE107867 cultured B-cells;ASD brains,cerebellum;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 24183664,30559470,30559470 RNA-Seq:(High) rs1022171429 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24003688 Human_miRNA_ID_2864853 RMVar_hsa_circ_82352,RMVar_hsa_circ_109506,RMVar_hsa_circ_106545,RMVar_hsa_circ_217337,RMVar_hsa_circ_217338,RMVar_hsa_circ_217339 43845 RMVar_ID_43845 Human_SNP_ID_131351876 A-to-I Human chr3 - 44749826 44749826 44749826 TGATTGCACCACTGCACTCCAGCCTGGGCAACAGAGTAAGAACTGTCTCAAAAAAAATAAAAAAT TGATTGCACCACTGCACTCCAGCCTGGGCAACCGAGTAAGAACTGTCTCAAAAAAAATAAAAAAT T G KIAA1143 Ensembl:ENSG00000163807 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs548642942 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82352,RMVar_hsa_circ_109506,RMVar_hsa_circ_106545,RMVar_hsa_circ_217337,RMVar_hsa_circ_217338,RMVar_hsa_circ_217339 43846 RMVar_ID_43846 Human_SNP_ID_131351882 A-to-I Human chr3 - 44749851 44749851 44749851 AGGAGTTCAACGCTGCAGTGAGCTATGATTGCACCACTGCACTCCAGCCTGGGCAACAGAGTAAG AGGAGTTCAACGCTGCAGTGAGCTATGATTGCGCCACTGCACTCCAGCCTGGGCAACAGAGTAAG T C KIAA1143 Ensembl:ENSG00000163807 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs377016950 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82352,RMVar_hsa_circ_109506,RMVar_hsa_circ_106545,RMVar_hsa_circ_217337,RMVar_hsa_circ_217338,RMVar_hsa_circ_217339 43847 RMVar_ID_43847 Human_SNP_ID_131351883 A-to-I Human chr3 - 44749859 44749859 44749859 TTGGGCCCAGGAGTTCAACGCTGCAGTGAGCTATGATTGCACCACTGCACTCCAGCCTGGGCAAC TTGGGCCCAGGAGTTCAACGCTGCAGTGAGCTGTGATTGCACCACTGCACTCCAGCCTGGGCAAC T C KIAA1143 Ensembl:ENSG00000163807 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229,31158229 RNA-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 43848 RMVar_ID_43848 Human_SNP_ID_131351884 A-to-I Human chr3 - 44749863 44749863 44749863 TGGCTTGGGCCCAGGAGTTCAACGCTGCAGTGAGCTATGATTGCACCACTGCACTCCAGCCTGGG TGGCTTGGGCCCAGGAGTTCAACGCTGCAGTGGGCTATGATTGCACCACTGCACTCCAGCCTGGG T C KIAA1143 Ensembl:ENSG00000163807 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1460536074 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82352,RMVar_hsa_circ_109506,RMVar_hsa_circ_106545,RMVar_hsa_circ_217337,RMVar_hsa_circ_217338,RMVar_hsa_circ_217339 43849 RMVar_ID_43849 Human_SNP_ID_131351896 A-to-I Human chr3 - 44749906 44749906 44749906 ACACACCTGTAGTCCCAGCTGCTCAGGAGGCTAAGCAGGAGGATGGCTTGGGCCCAGGAGTTCAA ACACACCTGTAGTCCCAGCTGCTCAGGAGGCTGAGCAGGAGGATGGCTTGGGCCCAGGAGTTCAA T C KIAA1143 Ensembl:ENSG00000163807 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs3205463 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 43850 RMVar_ID_43850 Human_SNP_ID_131351900 A-to-I Human chr3 - 44749914 44749914 44749914 GTAGCGACACACACCTGTAGTCCCAGCTGCTCAGGAGGCTAAGCAGGAGGATGGCTTGGGCCCAG GTAGCGACACACACCTGTAGTCCCAGCTGCTCGGGAGGCTAAGCAGGAGGATGGCTTGGGCCCAG T C KIAA1143 Ensembl:ENSG00000163807 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-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 43851 RMVar_ID_43851 Human_SNP_ID_131351928 A-to-I Human chr3 - 44750020 44750020 44750020 CTTTGGGAAGCCAAGGTGGGAGAATTGCTTGAAGCCAGGAATCTGAGCCCAGCCTGGGCGACAAA CTTTGGGAAGCCAAGGTGGGAGAATTGCTTGAGGCCAGGAATCTGAGCCCAGCCTGGGCGACAAA T C KIAA1143 Ensembl:ENSG00000163807 Protein coding intron GSE112787;GSE126723:GSM3611830,GSM3611831,GSM3611832 293 Flip-In T-REx cells,empty vector;Bronchiolar epithelium,BERP35T1 cell line - 29967493,31158229 RNA-Seq:(High) rs1250679322 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82352,RMVar_hsa_circ_109506,RMVar_hsa_circ_106545,RMVar_hsa_circ_217337,RMVar_hsa_circ_217338,RMVar_hsa_circ_217339 43852 RMVar_ID_43852 Human_SNP_ID_131351933 A-to-I Human chr3 - 44750044 44750044 44750044 TGGCTCATGCTTGTAATCCCAACACTTTGGGAAGCCAAGGTGGGAGAATTGCTTGAAGCCAGGAA TGGCTCATGCTTGTAATCCCAACACTTTGGGAGGCCAAGGTGGGAGAATTGCTTGAAGCCAGGAA T C KIAA1143 Ensembl:ENSG00000163807 Protein coding intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1257540447 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26512094 RMVar_hsa_circ_82352,RMVar_hsa_circ_109506,RMVar_hsa_circ_106545,RMVar_hsa_circ_217337,RMVar_hsa_circ_217338,RMVar_hsa_circ_217339 43853 RMVar_ID_43853 Human_SNP_ID_131351936 A-to-I Human chr3 - 44750062 44750062 44750062 CACCCAGGCCAGACACAATGGCTCATGCTTGTAATCCCAACACTTTGGGAAGCCAAGGTGGGAGA CACCCAGGCCAGACACAATGGCTCATGCTTGTGATCCCAACACTTTGGGAAGCCAAGGTGGGAGA T C KIAA1143 Ensembl:ENSG00000163807 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-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 43854 RMVar_ID_43854 Human_SNP_ID_131357568 A-to-I Human chr3 + 44775946 44775946 44775946 ACTAAAAATACAAAAAATTAGCTGGTTGTGGTAGTGGGCACCTGTAGTCCTAGCTACTCGGGAGG ACTAAAAATACAAAAAATTAGCTGGTTGTGGTGGTGGGCACCTGTAGTCCTAGCTACTCGGGAGG A G KIF15 Ensembl:ENSG00000163808 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1275313308 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1077,RMVar_hsa_circ_217340,RMVar_hsa_circ_87474,RMVar_hsa_circ_38547,RMVar_hsa_circ_297693,RMVar_hsa_circ_4801,RMVar_hsa_circ_19816,RMVar_hsa_circ_48926,RMVar_hsa_circ_325191,RMVar_hsa_circ_330304,RMVar_hsa_circ_321405,RMVar_hsa_circ_50785,RMVar_hsa_circ_22936,RMVar_hsa_circ_217341,RMVar_hsa_circ_217343,RMVar_hsa_circ_217342 43855 RMVar_ID_43855 Human_SNP_ID_131361342 A-to-I Human chr3 + 44792574 44792573 44792575 TACGAATTTTTTTTTTTTTTTTGTGATGAGACAGAGTCTCTGTTGCCCAGGCTGGAGCGGAATGG TACGAATTTTTTTTTTTTTTTTGTGATGAGAC__AGTCTCTGTTGCCCAGGCTGGAGCGGAATGG CAG C KIF15 Ensembl:ENSG00000163808 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1300632812 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_38547,RMVar_hsa_circ_4801,RMVar_hsa_circ_9699,RMVar_hsa_circ_46351,RMVar_hsa_circ_19816,RMVar_hsa_circ_48926,RMVar_hsa_circ_330304,RMVar_hsa_circ_22936,RMVar_hsa_circ_217341,RMVar_hsa_circ_67901,RMVar_hsa_circ_14090,RMVar_hsa_circ_33670,RMVar_hsa_circ_308504,RMVar_hsa_circ_344619,RMVar_hsa_circ_349538,RMVar_hsa_circ_307769,RMVar_hsa_circ_217345,RMVar_hsa_circ_217346,RMVar_hsa_circ_347351,RMVar_hsa_circ_348869,RMVar_hsa_circ_371038,RMVar_hsa_circ_343781,RMVar_hsa_circ_304991,RMVar_hsa_circ_290463,RMVar_hsa_circ_71015,RMVar_hsa_circ_217348,RMVar_hsa_circ_217349,RMVar_hsa_circ_217350,RMVar_hsa_circ_308071,RMVar_hsa_circ_325461,RMVar_hsa_circ_63874 43856 RMVar_ID_43856 Human_SNP_ID_131371189 A-to-I Human chr3 + 44832226 44832226 44832226 TGTGAACATGTGTGGAGTGTCCCAAGCACAGCAGGCAGTCAGGGTGGCCAATACAAGGTGCTGGC TGTGAACATGTGTGGAGTGTCCCAAGCACAGCGGGCAGTCAGGGTGGCCAATACAAGGTGCTGGC A G KIF15 Ensembl:ENSG00000163808 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1187051004 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5295,RMVar_hsa_circ_46351,RMVar_hsa_circ_71015,RMVar_hsa_circ_265609,RMVar_hsa_circ_217356,RMVar_hsa_circ_12101,RMVar_hsa_circ_107224,RMVar_hsa_circ_264992,RMVar_hsa_circ_44856,RMVar_hsa_circ_10049,RMVar_hsa_circ_217360,RMVar_hsa_circ_334142,RMVar_hsa_circ_117508,RMVar_hsa_circ_217361,RMVar_hsa_circ_16580,RMVar_hsa_circ_377860,RMVar_hsa_circ_36247,RMVar_hsa_circ_45707,RMVar_hsa_circ_281520,RMVar_hsa_circ_299376,RMVar_hsa_circ_284013,RMVar_hsa_circ_314106,RMVar_hsa_circ_217364,RMVar_hsa_circ_217365 43857 RMVar_ID_43857 Human_SNP_ID_131382382 A-to-I Human chr3 + 44879462 44879462 44879462 TCGAGTAGCTGGGATTACAGGCATGTGCCACCAAGCCTGGCTAATTTTTTTTTTTTTTTTTGAGA TCGAGTAGCTGGGATTACAGGCATGTGCCACCGAGCCTGGCTAATTTTTTTTTTTTTTTTTGAGA A G TGM4 Ensembl:ENSG00000163810 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1281896292 Functional Loss SNV dbSNP153 33..33 33 - - - 43858 RMVar_ID_43858 Human_SNP_ID_186470381 A-to-I Human chr4 + 61905626 61905626 61905626 AAGAATTTCTCGAAAGTTGGGCCAGGTGCAGTAGTTCACGCCTATGATCTCAGCACTTTGGGAGG AAGAATTTCTCGAAAGTTGGGCCAGGTGCAGTCGTTCACGCCTATGATCTCAGCACTTTGGGAGG A C ADGRL3 Ensembl:ENSG00000150471 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1360328865 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_752,RMVar_hsa_circ_14813,RMVar_hsa_circ_551,RMVar_hsa_circ_7070,RMVar_hsa_circ_343588,RMVar_hsa_circ_325545,RMVar_hsa_circ_304859,RMVar_hsa_circ_23994,RMVar_hsa_circ_39527,RMVar_hsa_circ_41750,RMVar_hsa_circ_88763,RMVar_hsa_circ_24427,RMVar_hsa_circ_14685,RMVar_hsa_circ_226303,RMVar_hsa_circ_299920,RMVar_hsa_circ_320011,RMVar_hsa_circ_319254,RMVar_hsa_circ_52476,RMVar_hsa_circ_279949,RMVar_hsa_circ_308638,RMVar_hsa_circ_325528,RMVar_hsa_circ_295644,RMVar_hsa_circ_41933,RMVar_hsa_circ_274527,RMVar_hsa_circ_226312,RMVar_hsa_circ_105874,RMVar_hsa_circ_226307,RMVar_hsa_circ_226309,RMVar_hsa_circ_9725,RMVar_hsa_circ_226310,RMVar_hsa_circ_226308,RMVar_hsa_circ_226306,RMVar_hsa_circ_30038,RMVar_hsa_circ_43249,RMVar_hsa_circ_226313,RMVar_hsa_circ_226314 43859 RMVar_ID_43859 Human_SNP_ID_188019134 A-to-I Human chr4 - 67453861 67453861 67453861 GGCAGAAGGTGAAGGGGAAGCAGGCATGTCTTACGTGGCCAGAGCAGGAGGAAGAGAAGGGAGTG GGCAGAAGGTGAAGGGGAAGCAGGCATGTCTTGCGTGGCCAGAGCAGGAGGAAGAGAAGGGAGTG T C AC104806.2 Ensembl:ENSG00000250075 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941437930 Functional Loss SNV dbSNP153 33..33 33 - - - 43860 RMVar_ID_43860 Human_SNP_ID_188024127 A-to-I Human chr4 - 67474515 67474513 67474515 TTTTGTATTTTTAGTAGAGGCGGGATTTTGCTATGTTAGCCGTAACAGATCACCTGACCTCAAGT TTTTGTATTTTTAGTAGAGGCGGGATTTTGCT__GTTAGCCGTAACAGATCACCTGACCTCAAGT CAT C CENPC Ensembl:ENSG00000145241 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1278758081 Functional Loss DEL dbSNP153 33..34 33 - - - 43861 RMVar_ID_43861 Human_SNP_ID_188024129 A-to-I Human chr4 - 67474515 67474515 67474515 TTTTGTATTTTTAGTAGAGGCGGGATTTTGCTATGTTAGCCGTAACAGATCACCTGACCTCAAGT TTTTGTATTTTTAGTAGAGGCGGGATTTTGCTGTGTTAGCCGTAACAGATCACCTGACCTCAAGT T C CENPC Ensembl:ENSG00000145241 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1420102504 Functional Loss SNV dbSNP153 33..33 33 - - - 43862 RMVar_ID_43862 Human_SNP_ID_188034749 A-to-I Human chr4 - 67517204 67517204 67517204 TGAGTCGAGACGGTGCCACTGCACTCTAGCCTAGGTGACAGAGTGAGACTCAGTCTCAAAAATAA TGAGTCGAGACGGTGCCACTGCACTCTAGCCTGGGTGACAGAGTGAGACTCAGTCTCAAAAATAA T C CENPC Ensembl:ENSG00000145241 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs535697534 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67913,RMVar_hsa_circ_309766,RMVar_hsa_circ_267272,RMVar_hsa_circ_360475 43863 RMVar_ID_43863 Human_SNP_ID_188034777 A-to-I Human chr4 - 67517330 67517330 67517330 TGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGTCGGGCTTGGTGGCACATGCCTGTAAT TGGTGAAACCCCATCTCTACTAAAAATACAAATATTAGTCGGGCTTGGTGGCACATGCCTGTAAT T A CENPC Ensembl:ENSG00000145241 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs961519517 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67913,RMVar_hsa_circ_309766,RMVar_hsa_circ_267272,RMVar_hsa_circ_360475 43864 RMVar_ID_43864 Human_SNP_ID_188051607 A-to-I Human chr4 + 67587862 67587849 67587862 CCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAAGCATGTGCCACCACGCCTGGCTAATTTTTTT CCTGCCTCAGCCTCCCGAGT_____________AGCATGTGCCACCACGCCTGGCTAATTTTTTT TAGCTGGGATTACA T STAP1 Ensembl:ENSG00000035720 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1325604203 Functional Loss DEL dbSNP153 21..33 33 - - - RMVar_hsa_circ_368459 43865 RMVar_ID_43865 Human_SNP_ID_188057084 A-to-I Human chr4 - 67610766 67610766 67610766 TGTGCTTCTCCTTTGCCATCTGGCTTGTTTTTAGGTCCTGCAAAGAAAGAGTACTAAGAGACTAG TGTGCTTCTCCTTTGCCATCTGGCTTGTTTTTGGGTCCTGCAAAGAAAGAGTACTAAGAGACTAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1190061938 Functional Loss SNV dbSNP153 33..33 33 - - - 43866 RMVar_ID_43866 Human_SNP_ID_188066140 A-to-I Human chr4 - 67647419 67647419 67647419 AATTATGACTGGGCGCAGTGGCTCATGCCTGTAATACCAGCACTTTGGGAGGCCGAGGTGGGCAG AATTATGACTGGGCGCAGTGGCTCATGCCTGTGATACCAGCACTTTGGGAGGCCGAGGTGGGCAG T C UBA6 Ensembl:ENSG00000033178 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1390077827 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77401,RMVar_hsa_circ_116126,RMVar_hsa_circ_127250,RMVar_hsa_circ_226384,RMVar_hsa_circ_226386,RMVar_hsa_circ_226385,RMVar_hsa_circ_113631,RMVar_hsa_circ_97724,RMVar_hsa_circ_226393,RMVar_hsa_circ_226394,RMVar_hsa_circ_226392,RMVar_hsa_circ_226396,RMVar_hsa_circ_118816,RMVar_hsa_circ_110259,RMVar_hsa_circ_13017,RMVar_hsa_circ_226395,RMVar_hsa_circ_344456,RMVar_hsa_circ_22824,RMVar_hsa_circ_49692,RMVar_hsa_circ_30542,RMVar_hsa_circ_226401,RMVar_hsa_circ_283443,RMVar_hsa_circ_123735,RMVar_hsa_circ_226404,RMVar_hsa_circ_112749,RMVar_hsa_circ_226405,RMVar_hsa_circ_226407,RMVar_hsa_circ_28382,RMVar_hsa_circ_42113,RMVar_hsa_circ_26762,RMVar_hsa_circ_81245,RMVar_hsa_circ_226410,RMVar_hsa_circ_106711,RMVar_hsa_circ_226412,RMVar_hsa_circ_226413,RMVar_hsa_circ_336005,RMVar_hsa_circ_350646,RMVar_hsa_circ_42958 43867 RMVar_ID_43867 Human_SNP_ID_188066387 A-to-I Human chr4 - 67648360 67648360 67648360 GGGTTCACGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGGTTACAGATGCAGACCACCACA GGGTTCACGCGATTCTCCTGCCTCAGCCTCCCTAGTAGCTGGGGTTACAGATGCAGACCACCACA T A UBA6 Ensembl:ENSG00000033178 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs933086050 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77401,RMVar_hsa_circ_116126,RMVar_hsa_circ_127250,RMVar_hsa_circ_226384,RMVar_hsa_circ_226386,RMVar_hsa_circ_226385,RMVar_hsa_circ_113631,RMVar_hsa_circ_97724,RMVar_hsa_circ_226393,RMVar_hsa_circ_226394,RMVar_hsa_circ_226392,RMVar_hsa_circ_226396,RMVar_hsa_circ_118816,RMVar_hsa_circ_110259,RMVar_hsa_circ_13017,RMVar_hsa_circ_226395,RMVar_hsa_circ_344456,RMVar_hsa_circ_22824,RMVar_hsa_circ_49692,RMVar_hsa_circ_30542,RMVar_hsa_circ_226401,RMVar_hsa_circ_283443,RMVar_hsa_circ_123735,RMVar_hsa_circ_226404,RMVar_hsa_circ_112749,RMVar_hsa_circ_226405,RMVar_hsa_circ_226407,RMVar_hsa_circ_28382,RMVar_hsa_circ_42113,RMVar_hsa_circ_26762,RMVar_hsa_circ_81245,RMVar_hsa_circ_226410,RMVar_hsa_circ_106711,RMVar_hsa_circ_226412,RMVar_hsa_circ_226413,RMVar_hsa_circ_336005,RMVar_hsa_circ_350646,RMVar_hsa_circ_42958 43868 RMVar_ID_43868 Human_SNP_ID_188066401 A-to-I Human chr4 - 67648405 67648405 67648405 GGAGTGCAATGGCGCGATGTTAGCTCACTGCAACCTCTGTCTGCCGGGTTCACGCGATTCTCCTG GGAGTGCAATGGCGCGATGTTAGCTCACTGCACCCTCTGTCTGCCGGGTTCACGCGATTCTCCTG T G UBA6 Ensembl:ENSG00000033178 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1411150810 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77401,RMVar_hsa_circ_116126,RMVar_hsa_circ_127250,RMVar_hsa_circ_226384,RMVar_hsa_circ_226386,RMVar_hsa_circ_226385,RMVar_hsa_circ_113631,RMVar_hsa_circ_97724,RMVar_hsa_circ_226393,RMVar_hsa_circ_226394,RMVar_hsa_circ_226392,RMVar_hsa_circ_226396,RMVar_hsa_circ_118816,RMVar_hsa_circ_110259,RMVar_hsa_circ_13017,RMVar_hsa_circ_226395,RMVar_hsa_circ_344456,RMVar_hsa_circ_22824,RMVar_hsa_circ_49692,RMVar_hsa_circ_30542,RMVar_hsa_circ_226401,RMVar_hsa_circ_283443,RMVar_hsa_circ_123735,RMVar_hsa_circ_226404,RMVar_hsa_circ_112749,RMVar_hsa_circ_226405,RMVar_hsa_circ_226407,RMVar_hsa_circ_28382,RMVar_hsa_circ_42113,RMVar_hsa_circ_26762,RMVar_hsa_circ_81245,RMVar_hsa_circ_226410,RMVar_hsa_circ_106711,RMVar_hsa_circ_226412,RMVar_hsa_circ_226413,RMVar_hsa_circ_336005,RMVar_hsa_circ_350646,RMVar_hsa_circ_42958 43869 RMVar_ID_43869 Human_SNP_ID_188070195 A-to-I Human chr4 - 67663207 67663207 67663207 GCCGATTTTTAATGTTCTCAATAGGCACCTTTAGAGATTCACACAGCTATGCTTGCCTTGGACCA GCCGATTTTTAATGTTCTCAATAGGCACCTTTGGAGATTCACACAGCTATGCTTGCCTTGGACCA T C UBA6 Ensembl:ENSG00000033178 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1221800254 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_565592,Human_Splice_Rec_565593,Human_Splice_Rec_565678,Human_Splice_Rec_565679 Human_miRNA_ID_616546,Human_miRNA_ID_2232214 RMVar_hsa_circ_77401,RMVar_hsa_circ_116126,RMVar_hsa_circ_127250,RMVar_hsa_circ_226384,RMVar_hsa_circ_226386,RMVar_hsa_circ_226385,RMVar_hsa_circ_113631,RMVar_hsa_circ_97724,RMVar_hsa_circ_226393,RMVar_hsa_circ_226394,RMVar_hsa_circ_226396,RMVar_hsa_circ_118816,RMVar_hsa_circ_110259,RMVar_hsa_circ_13017,RMVar_hsa_circ_226395,RMVar_hsa_circ_344456,RMVar_hsa_circ_123735,RMVar_hsa_circ_112749,RMVar_hsa_circ_226405,RMVar_hsa_circ_226407,RMVar_hsa_circ_28382,RMVar_hsa_circ_42113,RMVar_hsa_circ_25143,RMVar_hsa_circ_81245,RMVar_hsa_circ_106711,RMVar_hsa_circ_226412,RMVar_hsa_circ_226413,RMVar_hsa_circ_350646,RMVar_hsa_circ_42958,RMVar_hsa_circ_79271,RMVar_hsa_circ_274667,RMVar_hsa_circ_349336,RMVar_hsa_circ_115079,RMVar_hsa_circ_78245,RMVar_hsa_circ_89158,RMVar_hsa_circ_59865,RMVar_hsa_circ_226415,RMVar_hsa_circ_226416,RMVar_hsa_circ_226417,RMVar_hsa_circ_226414,RMVar_hsa_circ_289957,RMVar_hsa_circ_41822,RMVar_hsa_circ_58001,RMVar_hsa_circ_124822,RMVar_hsa_circ_226418,RMVar_hsa_circ_226419,RMVar_hsa_circ_226420,RMVar_hsa_circ_330038 43870 RMVar_ID_43870 Human_SNP_ID_188101300 A-to-I Human chr4 + 67794602 67794602 67794602 CTCGTGCCTCAGCCTCCAGAGTAGTTGAGACTACAGGCACCCGCTACCATGCCCAGATAATTTCT CTCGTGCCTCAGCCTCCAGAGTAGTTGAGACTCCAGGCACCCGCTACCATGCCCAGATAATTTCT A C UBA6-AS1 Ensembl:ENSG00000248049 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1445004522 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_226430,RMVar_hsa_circ_226438,RMVar_hsa_circ_226440,RMVar_hsa_circ_226441,RMVar_hsa_circ_226439 43871 RMVar_ID_43871 Human_SNP_ID_188229183 A-to-I Human chr4 - 68317112 68317112 68317112 ACAAGTGGTCCTGCTGCCTCAGCTTCCTGAGTAGGTGGGACTACAGGCACATGCCACTGTGCCTG ACAAGTGGTCCTGCTGCCTCAGCTTCCTGAGTGGGTGGGACTACAGGCACATGCCACTGTGCCTG T C YTHDC1 Ensembl:ENSG00000083896 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs146572511 Functional Loss SNV dbSNP153 33..33 33 - - - 43872 RMVar_ID_43872 Human_SNP_ID_188231627 A-to-I Human chr4 - 68327205 68327205 68327205 TGAGACGGAGTTTCGCTCTTGTTGCCCAGGCTAGAGTGCAATGGCGCAATCTCGGCTCACCACAA TGAGACGGAGTTTCGCTCTTGTTGCCCAGGCTGGAGTGCAATGGCGCAATCTCGGCTCACCACAA T C YTHDC1 Ensembl:ENSG00000083896 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs562786000 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55246,RMVar_hsa_circ_226445,RMVar_hsa_circ_369553 43873 RMVar_ID_43873 Human_SNP_ID_188233816 A-to-I Human chr4 - 68335930 68335930 68335930 GTATAGGTAGAGCAGATGGCCAGTTATTTTCTAGTGATTGGCAACTGAAGTGCTTTCAACCTTTT GTATAGGTAGAGCAGATGGCCAGTTATTTTCTCGTGATTGGCAACTGAAGTGCTTTCAACCTTTT T G YTHDC1 Ensembl:ENSG00000083896 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs916243718 Functional Loss SNV dbSNP153 33..33 33 - - - 43874 RMVar_ID_43874 Human_SNP_ID_188244115 A-to-I Human chr4 + 68376350 68376350 68376350 TCGCCATGGATCCCAACTGCTCCTGTGCCGCCAGTGACTCCTGCACCTGCGCCGGCTCCTGCAAG TCGCCATGGATCCCAACTGCTCCTGTGCCGCCGGTGACTCCTGCACCTGCGCCGGCTCCTGCAAG A G MT2P1 Ensembl:ENSG00000162840 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs768785878 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8265938 43875 RMVar_ID_43875 Human_SNP_ID_188244116 A-to-I Human chr4 + 68376350 68376350 68376350 TCGCCATGGATCCCAACTGCTCCTGTGCCGCCAGTGACTCCTGCACCTGCGCCGGCTCCTGCAAG TCGCCATGGATCCCAACTGCTCCTGTGCCGCCTGTGACTCCTGCACCTGCGCCGGCTCCTGCAAG A T MT2P1 Ensembl:ENSG00000162840 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs768785878 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8265938 43876 RMVar_ID_43876 Human_SNP_ID_188536766 A-to-I Human chr4 - 69431016 69431016 69431016 AAGAGAAGAAACAGACGGTGGCCATGGAAGTCAGAATCCGCTAAGGAGTGTGTAACAACTCACCT AAGAGAAGAAACAGACGGTGGCCATGGAAGTCGGAATCCGCTAAGGAGTGTGTAACAACTCACCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs9715715 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_270603,Human_RBP_ID_283427,Human_RBP_ID_1037032,Human_RBP_ID_1107740,Human_RBP_ID_2854758,Human_RBP_ID_4789063,Human_RBP_ID_5212543,Human_RBP_ID_5276322,Human_RBP_ID_5426509,Human_RBP_ID_5448873,Human_RBP_ID_5475672,Human_RBP_ID_5508203,Human_RBP_ID_7323110,Human_RBP_ID_8128775,Human_RBP_ID_8594054,Human_RBP_ID_8880712,Human_RBP_ID_9165860,Human_RBP_ID_10153118,Human_RBP_ID_17031515,Human_RBP_ID_17069624,Human_RBP_ID_17154305,Human_RBP_ID_17196038,Human_RBP_ID_17295124,Human_RBP_ID_17524685,Human_RBP_ID_17706081,Human_RBP_ID_18033411,Human_RBP_ID_18182904,Human_RBP_ID_18201941,Human_RBP_ID_18210343,Human_RBP_ID_18348763,Human_RBP_ID_18447665,Human_RBP_ID_20977511,Human_RBP_ID_22401928,Human_RBP_ID_22423644,Human_RBP_ID_22510883,Human_RBP_ID_23136113,Human_RBP_ID_23289673,Human_RBP_ID_23313437,Human_RBP_ID_24062262,Human_RBP_ID_26518943,Human_RBP_ID_26750917,Human_RBP_ID_27160155,Human_RBP_ID_27328228,Human_RBP_ID_27509084,Human_RBP_ID_27566963,Human_RBP_ID_27729451 43877 RMVar_ID_43877 Human_SNP_ID_188627050 A-to-I Human chr4 - 69756853 69756853 69756853 AATGGGACTCACGCAATCAGTTGAAGGCCTGAATAGAACCAAAAGGGTGACTCTCCTGGAAGTAA AATGGGACTCACGCAATCAGTTGAAGGCCTGAGTAGAACCAAAAGGGTGACTCTCCTGGAAGTAA T C SULT1B1 Ensembl:ENSG00000173597 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1207370577 Functional Loss SNV dbSNP153 33..33 33 - - - 43878 RMVar_ID_43878 Human_SNP_ID_188876504 A-to-I Human chr4 + 70707320 70707320 70707320 TCGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCATGACCTCTGCTCACTGCAACCTCCGCCTCCCG TCGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCGTGACCTCTGCTCACTGCAACCTCCGCCTCCCG A G RUFY3 Ensembl:ENSG00000018189 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1222926241 Functional Loss SNV dbSNP153 33..33 33 - - - 43879 RMVar_ID_43879 Human_SNP_ID_188876649 A-to-I Human chr4 + 70708038 70708038 70708038 CCCAGCCCTTTGGGAGACTAAGGTGAAGGATCACTTGAGTCCAGAAGTTCAGGGCTGCAGTAAGC CCCAGCCCTTTGGGAGACTAAGGTGAAGGATCTCTTGAGTCCAGAAGTTCAGGGCTGCAGTAAGC A T RUFY3 Ensembl:ENSG00000018189 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1458627786 Functional Loss SNV dbSNP153 33..33 33 - - - 43880 RMVar_ID_43880 Human_SNP_ID_188898023 A-to-I Human chr4 + 70797106 70797106 70797106 GGGACTGTAGGCACACACCACAAAACTCAGCTAATTTTTGTATTTTTTTGGTAGAGTCAGGGTTT GGGACTGTAGGCACACACCACAAAACTCAGCTGATTTTTGTATTTTTTTGGTAGAGTCAGGGTTT A G RUFY3 Ensembl:ENSG00000018189 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs948281893 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_161893 RMVar_hsa_circ_54708 43881 RMVar_ID_43881 Human_SNP_ID_188898040 A-to-I Human chr4 + 70797195 70797195 70797195 CAACTCCTGGGCTCAAGCGATATGCCTGCCTCAGCCTCCCAAAGTGCTAGGATGACAGGCATGAG CAACTCCTGGGCTCAAGCGATATGCCTGCCTCCGCCTCCCAAAGTGCTAGGATGACAGGCATGAG A C RUFY3 Ensembl:ENSG00000018189 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs950170236 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25818051 RMVar_hsa_circ_54708 43882 RMVar_ID_43882 Human_SNP_ID_188899874 A-to-I Human chr4 + 70804831 70804831 70804831 CCTGTAATCCCAGCTACTCAGGTTGCTGAGGCAGGAGAATCGCTTGAACCCGGGAGGCGGAGGTT CCTGTAATCCCAGCTACTCAGGTTGCTGAGGCGGGAGAATCGCTTGAACCCGGGAGGCGGAGGTT A G RUFY3 Ensembl:ENSG00000018189 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1043567608 Functional Loss SNV dbSNP153 33..33 33 - - - 43883 RMVar_ID_43883 Human_SNP_ID_188900497 A-to-I Human chr4 + 70807689 70807689 70807689 GACTGGCTTTTTTTTTTTTTTTTTGGCCGGGGAGGGGGTCTCATTGGTTGCTCAGCCTGGTCTCA GACTGGCTTTTTTTTTTTTTTTTTGGCCGGGGGGGGGGTCTCATTGGTTGCTCAGCCTGGTCTCA A G RUFY3 Ensembl:ENSG00000018189 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1002611120 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_623507,Human_RBP_ID_7323687,Human_RBP_ID_18028783 43884 RMVar_ID_43884 Human_SNP_ID_188902725 A-to-I Human chr4 - 70816267 70816267 70816267 TGGCTCACTGCAACCTCCACCTCCTGGGTTCAAGGGAGTCTCCTGCCTCAGCCTCCCGAGTAGCT TGGCTCACTGCAACCTCCACCTCCTGGGTTCAGGGGAGTCTCCTGCCTCAGCCTCCCGAGTAGCT T C GRSF1 Ensembl:ENSG00000132463 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1013403750 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85590,RMVar_hsa_circ_226465 43885 RMVar_ID_43885 Human_SNP_ID_188902729 A-to-I Human chr4 - 70816281 70816281 70816281 CAGTGGCCTGGTCTTGGCTCACTGCAACCTCCACCTCCTGGGTTCAAGGGAGTCTCCTGCCTCAG CAGTGGCCTGGTCTTGGCTCACTGCAACCTCCGCCTCCTGGGTTCAAGGGAGTCTCCTGCCTCAG T C GRSF1 Ensembl:ENSG00000132463 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1253626886 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85590,RMVar_hsa_circ_226465 43886 RMVar_ID_43886 Human_SNP_ID_188902732 A-to-I Human chr4 - 70816287 70816287 70816287 AGAGTGCAGTGGCCTGGTCTTGGCTCACTGCAACCTCCACCTCCTGGGTTCAAGGGAGTCTCCTG AGAGTGCAGTGGCCTGGTCTTGGCTCACTGCAGCCTCCACCTCCTGGGTTCAAGGGAGTCTCCTG T C GRSF1 Ensembl:ENSG00000132463 Protein coding 3'UTR GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1184558181 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85590,RMVar_hsa_circ_226465 43887 RMVar_ID_43887 Human_SNP_ID_188902738 A-to-I Human chr4 - 70816319 70816319 70816319 TTTTTGAGATGGAGTCTTGTATCGCCCAGGCTAGAGTGCAGTGGCCTGGTCTTGGCTCACTGCAA TTTTTGAGATGGAGTCTTGTATCGCCCAGGCTGGAGTGCAGTGGCCTGGTCTTGGCTCACTGCAA T C GRSF1 Ensembl:ENSG00000132463 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1247846064 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85590,RMVar_hsa_circ_226465 43888 RMVar_ID_43888 Human_SNP_ID_188902873 A-to-I Human chr4 - 70816715 70816715 70816715 TTGTTTTTGTTTTTGTTTTTTGTGTTTGAGACAGTCGCTCTGTCACCCAGGCTGGAGTTATAGTG TTGTTTTTGTTTTTGTTTTTTGTGTTTGAGACTGTCGCTCTGTCACCCAGGCTGGAGTTATAGTG T A GRSF1 Ensembl:ENSG00000132463 Protein coding 3'UTR GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs575495381 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7323734,Human_RBP_ID_15190566 RMVar_hsa_circ_85590,RMVar_hsa_circ_226465 43889 RMVar_ID_43889 Human_SNP_ID_188902874 A-to-I Human chr4 - 70816715 70816715 70816715 TTGTTTTTGTTTTTGTTTTTTGTGTTTGAGACAGTCGCTCTGTCACCCAGGCTGGAGTTATAGTG TTGTTTTTGTTTTTGTTTTTTGTGTTTGAGACGGTCGCTCTGTCACCCAGGCTGGAGTTATAGTG T C GRSF1 Ensembl:ENSG00000132463 Protein coding 3'UTR GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs575495381 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7323734,Human_RBP_ID_15190566 RMVar_hsa_circ_85590,RMVar_hsa_circ_226465 43890 RMVar_ID_43890 Human_SNP_ID_188903051 A-to-I Human chr4 - 70817286 70817286 70817286 AGGACTGCTTGAGCCTGGGAAGTCAAGCCTGCAGTGAGCCATGACTGTTGCTGCACTCCAGCCTG AGGACTGCTTGAGCCTGGGAAGTCAAGCCTGCGGTGAGCCATGACTGTTGCTGCACTCCAGCCTG T C GRSF1 Ensembl:ENSG00000132463 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank;ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1009445711 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15190578 Human_miRNA_ID_2025825,Human_miRNA_ID_2215468 RMVar_hsa_circ_85590,RMVar_hsa_circ_226465 43891 RMVar_ID_43891 Human_SNP_ID_188903056 A-to-I Human chr4 - 70817318 70817311 70817318 GTAATCCCCGCACTTTGTGAGGCTGAAGTGGGAGGACTGCTTGAGCCTGGGAAGTCAAGCCTGCA GTAATCCCCGCACTTTGTGAGGCTGAAGTGGG_______CTTGAGCCTGGGAAGTCAAGCCTGCA GCAGTCCT G GRSF1 Ensembl:ENSG00000132463 Protein coding 3'UTR GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1201770986 Functional Loss DEL dbSNP153 33..39 33 - - - Human_RBP_ID_15190582 RMVar_hsa_circ_85590,RMVar_hsa_circ_226465 43892 RMVar_ID_43892 Human_SNP_ID_188903304 A-to-I Human chr4 - 70818154 70818154 70818154 CACGCCTGTAATCCCAGTTACTTGGGAGGCCAAGGCAGGAGAATCGCTTGAACCTGGGAGGCAGA CACGCCTGTAATCCCAGTTACTTGGGAGGCCATGGCAGGAGAATCGCTTGAACCTGGGAGGCAGA T A GRSF1 Ensembl:ENSG00000132463 Protein coding 3'UTR GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs895387593 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85590,RMVar_hsa_circ_226465 43893 RMVar_ID_43893 Human_SNP_ID_188903305 A-to-I Human chr4 - 70818154 70818154 70818154 CACGCCTGTAATCCCAGTTACTTGGGAGGCCAAGGCAGGAGAATCGCTTGAACCTGGGAGGCAGA CACGCCTGTAATCCCAGTTACTTGGGAGGCCAGGGCAGGAGAATCGCTTGAACCTGGGAGGCAGA T C GRSF1 Ensembl:ENSG00000132463 Protein coding 3'UTR GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs895387593 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85590,RMVar_hsa_circ_226465 43894 RMVar_ID_43894 Human_SNP_ID_188903317 A-to-I Human chr4 - 70818212 70818212 70818212 GGCCAACTTAGTGAAACTCCGGCTCTACTGAAAATGCAAAAATTAGCCAGGTGTGGCACACGCCT GGCCAACTTAGTGAAACTCCGGCTCTACTGAAGATGCAAAAATTAGCCAGGTGTGGCACACGCCT T C GRSF1 Ensembl:ENSG00000132463 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1431681361 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_981011,Human_miRNA_ID_985733,Human_miRNA_ID_2004490 RMVar_hsa_circ_85590,RMVar_hsa_circ_226465 43895 RMVar_ID_43895 Human_SNP_ID_188903813 A-to-I Human chr4 - 70820099 70820099 70820099 CCTAAGGGTGTTTGTTAGTCTCAAAACTGTGAAGTGACATGTCAGAACAGTCCAGACTGGTAAGA CCTAAGGGTGTTTGTTAGTCTCAAAACTGTGAGGTGACATGTCAGAACAGTCCAGACTGGTAAGA T C GRSF1 Ensembl:ENSG00000132463 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs866159120 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_623560,Human_RBP_ID_1106824,Human_RBP_ID_1980445,Human_RBP_ID_7323776,Human_RBP_ID_8880776,Human_RBP_ID_9162441,Human_RBP_ID_15190674,Human_RBP_ID_18028808,Human_RBP_ID_18826026,Human_RBP_ID_26516504 Human_miRNA_ID_1980228,Human_miRNA_ID_1981954,Human_miRNA_ID_2284859,Human_miRNA_ID_2287858 RMVar_hsa_circ_85590,RMVar_hsa_circ_226465 43896 RMVar_ID_43896 Human_SNP_ID_188904102 A-to-I Human chr4 - 70821210 70821210 70821210 GTTGGCCGGGTTGGTCTCGAACTCCTGACCTCAGCTGATCTGCCCGCCTCAACCTCCCAAAGTGC GTTGGCCGGGTTGGTCTCGAACTCCTGACCTCGGCTGATCTGCCCGCCTCAACCTCCCAAAGTGC T C GRSF1 Ensembl:ENSG00000132463 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1363921268 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85590,RMVar_hsa_circ_226465 43897 RMVar_ID_43897 Human_SNP_ID_188904346 A-to-I Human chr4 - 70821935 70821935 70821935 ATGGTGGGTTACTCCAGTAATCCCATTACTTCAGGAGGCTGAGGCAGGCAGATCACCTGAGGTCA ATGGTGGGTTACTCCAGTAATCCCATTACTTCGGGAGGCTGAGGCAGGCAGATCACCTGAGGTCA T C GRSF1 Ensembl:ENSG00000132463 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1203503608 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25818165 RMVar_hsa_circ_85590,RMVar_hsa_circ_226465 43898 RMVar_ID_43898 Human_SNP_ID_188904651 A-to-I Human chr4 - 70822929 70822929 70822929 CAATGCCTGGCTAATTTTTTTGTATTTTTAGTAGAGATGAGGTTTCACCATGTTGGCCAGGCTCA CAATGCCTGGCTAATTTTTTTGTATTTTTAGTGGAGATGAGGTTTCACCATGTTGGCCAGGCTCA T C GRSF1 Ensembl:ENSG00000132463 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1013643246 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85590,RMVar_hsa_circ_226465 43899 RMVar_ID_43899 Human_SNP_ID_188906563 A-to-I Human chr4 - 70829166 70829166 70829166 GGAAACTGTGCTGGGCGCGGTGGCCCATGCCTATAATCCCAGCACTTTGGGAGGCCGAAGTGGGA GGAAACTGTGCTGGGCGCGGTGGCCCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAAGTGGGA T C GRSF1 Ensembl:ENSG00000132463 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1047742593 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_292100,RMVar_hsa_circ_116011,RMVar_hsa_circ_368019,RMVar_hsa_circ_226469,RMVar_hsa_circ_226467,RMVar_hsa_circ_226468,RMVar_hsa_circ_289580,RMVar_hsa_circ_226470,RMVar_hsa_circ_356214,RMVar_hsa_circ_283224 43900 RMVar_ID_43900 Human_SNP_ID_188906687 A-to-I Human chr4 - 70829567 70829567 70829567 TCACTGCAGTTGTGGCCTCCTGGGCTCAAGCAATCCTCCCACTTCAGCCTCCCAAGTAGCTGGGA TCACTGCAGTTGTGGCCTCCTGGGCTCAAGCAGTCCTCCCACTTCAGCCTCCCAAGTAGCTGGGA T C GRSF1 Ensembl:ENSG00000132463 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs551441474 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_292100,RMVar_hsa_circ_116011,RMVar_hsa_circ_368019,RMVar_hsa_circ_226469,RMVar_hsa_circ_226467,RMVar_hsa_circ_226468,RMVar_hsa_circ_289580,RMVar_hsa_circ_226470,RMVar_hsa_circ_356214,RMVar_hsa_circ_283224 43901 RMVar_ID_43901 Human_SNP_ID_188906837 A-to-I Human chr4 - 70830177 70830177 70830177 AGTGATCGCCCGCTTTGGCTTCCCAAAACGCTAGGATTACAGGTGTGAGCCACTGCACCTGACCA AGTGATCGCCCGCTTTGGCTTCCCAAAACGCTGGGATTACAGGTGTGAGCCACTGCACCTGACCA T C GRSF1 Ensembl:ENSG00000132463 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1448557200 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15190976 RMVar_hsa_circ_292100,RMVar_hsa_circ_116011,RMVar_hsa_circ_368019,RMVar_hsa_circ_226469,RMVar_hsa_circ_226467,RMVar_hsa_circ_226468,RMVar_hsa_circ_289580,RMVar_hsa_circ_226470,RMVar_hsa_circ_356214,RMVar_hsa_circ_283224 43902 RMVar_ID_43902 Human_SNP_ID_188906859 A-to-I Human chr4 - 70830259 70830259 70830259 ATGTGTGTGTGCGTGCGTGCGTGTGTGTTTGTAGGTGGGGTCTTGCTGTGTTGCCCTGGCTGGCC ATGTGTGTGTGCGTGCGTGCGTGTGTGTTTGTCGGTGGGGTCTTGCTGTGTTGCCCTGGCTGGCC T G GRSF1 Ensembl:ENSG00000132463 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs890326781 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_785927,Human_RBP_ID_5655068,Human_RBP_ID_24062813,Human_RBP_ID_25818222 RMVar_hsa_circ_292100,RMVar_hsa_circ_116011,RMVar_hsa_circ_368019,RMVar_hsa_circ_226469,RMVar_hsa_circ_226467,RMVar_hsa_circ_226468,RMVar_hsa_circ_289580,RMVar_hsa_circ_226470,RMVar_hsa_circ_356214,RMVar_hsa_circ_283224 43903 RMVar_ID_43903 Human_SNP_ID_188906900 A-to-I Human chr4 - 70830329 70830329 70830329 GCAATCGTCTCGCCTCATCCTCCCAACTAGCTAGAACAATAGGCATGTGCCGCCACACCTGGCTG GCAATCGTCTCGCCTCATCCTCCCAACTAGCTGGAACAATAGGCATGTGCCGCCACACCTGGCTG T C GRSF1 Ensembl:ENSG00000132463 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1424536886 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8594162,Human_RBP_ID_15190977 RMVar_hsa_circ_292100,RMVar_hsa_circ_116011,RMVar_hsa_circ_368019,RMVar_hsa_circ_226469,RMVar_hsa_circ_226467,RMVar_hsa_circ_226468,RMVar_hsa_circ_289580,RMVar_hsa_circ_226470,RMVar_hsa_circ_356214,RMVar_hsa_circ_283224 43904 RMVar_ID_43904 Human_SNP_ID_188906919 A-to-I Human chr4 - 70830385 70830385 70830385 GCTGGAGTGCAGTGGCATGATGATAGCTCACTACAGCCTTGAATTCCTGGGCTCAAGCAATCGTC GCTGGAGTGCAGTGGCATGATGATAGCTCACTGCAGCCTTGAATTCCTGGGCTCAAGCAATCGTC T C GRSF1 Ensembl:ENSG00000132463 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1301088881 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_292100,RMVar_hsa_circ_116011,RMVar_hsa_circ_368019,RMVar_hsa_circ_226469,RMVar_hsa_circ_226467,RMVar_hsa_circ_226468,RMVar_hsa_circ_289580,RMVar_hsa_circ_226470,RMVar_hsa_circ_356214,RMVar_hsa_circ_283224 43905 RMVar_ID_43905 Human_SNP_ID_188907042 A-to-I Human chr4 - 70830646 70830646 70830646 CCCAGCTAAGTTTTGTATTTTTAGTAGAGACAAGGTTTTACCATGTTGGCCAGGCTGGTCTAGAA CCCAGCTAAGTTTTGTATTTTTAGTAGAGACAGGGTTTTACCATGTTGGCCAGGCTGGTCTAGAA T C GRSF1 Ensembl:ENSG00000132463 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1307933350 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_292100,RMVar_hsa_circ_116011,RMVar_hsa_circ_368019,RMVar_hsa_circ_226469,RMVar_hsa_circ_226467,RMVar_hsa_circ_226468,RMVar_hsa_circ_289580,RMVar_hsa_circ_226470,RMVar_hsa_circ_356214,RMVar_hsa_circ_283224 43906 RMVar_ID_43906 Human_SNP_ID_188907064 A-to-I Human chr4 - 70830743 70830743 70830743 TCTTGGCTCACTGCATCCTCTCTCTGCCTCCCAGTTTCATGTGATCCTCCTGCCTCAGCCTCCTG TCTTGGCTCACTGCATCCTCTCTCTGCCTCCCGGTTTCATGTGATCCTCCTGCCTCAGCCTCCTG T C GRSF1 Ensembl:ENSG00000132463 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs961322495 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15190995 RMVar_hsa_circ_292100,RMVar_hsa_circ_116011,RMVar_hsa_circ_368019,RMVar_hsa_circ_226469,RMVar_hsa_circ_226467,RMVar_hsa_circ_226468,RMVar_hsa_circ_289580,RMVar_hsa_circ_226470,RMVar_hsa_circ_356214,RMVar_hsa_circ_283224 43907 RMVar_ID_43907 Human_SNP_ID_188907198 A-to-I Human chr4 - 70831113 70831113 70831113 GACCTTGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCATC GACCTTGTGATCCGCCCGCCTCGGCCTCCCAAGGTGCTGGGATTACAGGCGTGAGCCACCGCATC T C GRSF1 Ensembl:ENSG00000132463 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1277848132 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_292100,RMVar_hsa_circ_116011,RMVar_hsa_circ_368019,RMVar_hsa_circ_226469,RMVar_hsa_circ_226467,RMVar_hsa_circ_226468,RMVar_hsa_circ_289580,RMVar_hsa_circ_226470,RMVar_hsa_circ_356214,RMVar_hsa_circ_283224 43908 RMVar_ID_43908 Human_SNP_ID_188909038 A-to-I Human chr4 - 70836967 70836967 70836967 CATTGAGCTCCACACTCAAGGCCCTCTGCTCTATGGTACCAACCTCTTTTGCCAGGTCACCTTCT CATTGAGCTCCACACTCAAGGCCCTCTGCTCTGTGGTACCAACCTCTTTTGCCAGGTCACCTTCT T C GRSF1 Ensembl:ENSG00000132463 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs3775729 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5011,GWAS_ID_5012 RMVar_hsa_circ_101090,RMVar_hsa_circ_80140,RMVar_hsa_circ_226472,RMVar_hsa_circ_226474 43909 RMVar_ID_43909 Human_SNP_ID_188909176 A-to-I Human chr4 - 70837442 70837442 70837442 ATCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACGGGCACACGCCACCACACCCGGCTCATTTTT ATCCTGCCTCAGCCTCCCGAGTAGCTGGGATTGCGGGCACACGCCACCACACCCGGCTCATTTTT T C GRSF1 Ensembl:ENSG00000132463 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1404415038 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101090,RMVar_hsa_circ_80140,RMVar_hsa_circ_226472,RMVar_hsa_circ_226474 43910 RMVar_ID_43910 Human_SNP_ID_188938654 A-to-I Human chr4 + 70951742 70951742 70951742 CAACAAAGTGAGACCTCATCTCTAATAAAAATACAAAAAATTAGCTGGGTGTGGTGGCGTAGTCA CAACAAAGTGAGACCTCATCTCTAATAAAAATTCAAAAAATTAGCTGGGTGTGGTGGCGTAGTCA A T MOB1B Ensembl:ENSG00000173542 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1221341160 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_226476,RMVar_hsa_circ_341127,RMVar_hsa_circ_320010,RMVar_hsa_circ_226478,RMVar_hsa_circ_300479,RMVar_hsa_circ_321562,RMVar_hsa_circ_336365,RMVar_hsa_circ_310101,RMVar_hsa_circ_226479,RMVar_hsa_circ_226477 43911 RMVar_ID_43911 Human_SNP_ID_189474209 A-to-I Human chr4 - 73056864 73056864 73056864 TGCCCACCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGTGCCCAGCTGAGATGT TGCCCACCTTGGCCTCCCAAAGTGCTGGGATTGCAGGCGTGAGCCACTGTGCCCAGCTGAGATGT T C COX18 Ensembl:ENSG00000163626 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1132044 Functional Loss SNV dbSNP153 33..33 33 - - - 43912 RMVar_ID_43912 Human_SNP_ID_189474221 A-to-I Human chr4 - 73056903 73056903 73056903 TTGGCTAGGCTGGTCTTGAACTCCTGGCCTCAAGTGATCTGCCCACCTTGGCCTCCCAAAGTGCT TTGGCTAGGCTGGTCTTGAACTCCTGGCCTCAGGTGATCTGCCCACCTTGGCCTCCCAAAGTGCT T C COX18 Ensembl:ENSG00000163626 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1132043 Functional Loss SNV dbSNP153 33..33 33 - - - 43913 RMVar_ID_43913 Human_SNP_ID_189474237 A-to-I Human chr4 - 73056955 73056955 73056955 CACCATGCCCAGCTAAGTTTTGTATTTTTAGTAGAGATGGGATTTCACCATGTTGGCTAGGCTGG CACCATGCCCAGCTAAGTTTTGTATTTTTAGTGGAGATGGGATTTCACCATGTTGGCTAGGCTGG T C COX18 Ensembl:ENSG00000163626 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,31158229,31158229,32596459 RNA-Seq:(High) rs953607674 Functional Loss SNV dbSNP153 33..33 33 - - - 43914 RMVar_ID_43914 Human_SNP_ID_189474254 A-to-I Human chr4 - 73057034 73057034 73057034 TCACTGCAACCTCTGCCTCCCGTGTTCAAGCAATTCTCCTACCTCAGCCTACTGGGTAGCTGGGA TCACTGCAACCTCTGCCTCCCGTGTTCAAGCAGTTCTCCTACCTCAGCCTACTGGGTAGCTGGGA T C COX18 Ensembl:ENSG00000163626 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1331309383 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26516594 Human_miRNA_ID_628348 43915 RMVar_ID_43915 Human_SNP_ID_189474255 A-to-I Human chr4 - 73057034 73057034 73057034 TCACTGCAACCTCTGCCTCCCGTGTTCAAGCAATTCTCCTACCTCAGCCTACTGGGTAGCTGGGA TCACTGCAACCTCTGCCTCCCGTGTTCAAGCACTTCTCCTACCTCAGCCTACTGGGTAGCTGGGA T G COX18 Ensembl:ENSG00000163626 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1331309383 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26516594 Human_miRNA_ID_628348 43916 RMVar_ID_43916 Human_SNP_ID_189474256 A-to-I Human chr4 - 73057039 73057039 73057039 TCGGCTCACTGCAACCTCTGCCTCCCGTGTTCAAGCAATTCTCCTACCTCAGCCTACTGGGTAGC TCGGCTCACTGCAACCTCTGCCTCCCGTGTTCCAGCAATTCTCCTACCTCAGCCTACTGGGTAGC T G COX18 Ensembl:ENSG00000163626 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1259986997 Functional Loss SNV dbSNP153 33..33 33 - - - 43917 RMVar_ID_43917 Human_SNP_ID_189474323 A-to-I Human chr4 - 73057201 73057201 73057201 GCTGGTCTGGAACTGCTGACCTCAACTAATCCACCCTCCTTGGCCTCCCATAGTGCTGGGATTAC GCTGGTCTGGAACTGCTGACCTCAACTAATCCGCCCTCCTTGGCCTCCCATAGTGCTGGGATTAC T C COX18 Ensembl:ENSG00000163626 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1386659120 Functional Loss SNV dbSNP153 33..33 33 - - - 43918 RMVar_ID_43918 Human_SNP_ID_189474339 A-to-I Human chr4 - 73057261 73057261 73057261 CACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGACAGGCTGG CACCACGCCCAGCTAATTTTTGTATTTTTAGTTGAGATGGGGTTTCACCATGTTGGACAGGCTGG T A COX18 Ensembl:ENSG00000163626 Protein coding 3'UTR GSE47997;GSE38233;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;cultured B-cells;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,24183664,29796672,31158229,31158229,31158229 RNA-Seq:(High) rs558042871 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4789666 43919 RMVar_ID_43919 Human_SNP_ID_189474340 A-to-I Human chr4 - 73057261 73057261 73057261 CACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGACAGGCTGG CACCACGCCCAGCTAATTTTTGTATTTTTAGTGGAGATGGGGTTTCACCATGTTGGACAGGCTGG T C COX18 Ensembl:ENSG00000163626 Protein coding 3'UTR GSE47997;GSE38233;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;cultured B-cells;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,24183664,29796672,31158229,31158229,31158229 RNA-Seq:(High) rs558042871 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4789666 43920 RMVar_ID_43920 Human_SNP_ID_189474356 A-to-I Human chr4 - 73057318 73057318 73057318 GGATTCCAGTGATTTTCCTGCCTCAGCCTCCAAGTATCTGGGATTGCAGGTGCACACCACCACGC GGATTCCAGTGATTTTCCTGCCTCAGCCTCCACGTATCTGGGATTGCAGGTGCACACCACCACGC T G COX18 Ensembl:ENSG00000163626 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1414639657 Functional Loss SNV dbSNP153 33..33 33 - - - 43921 RMVar_ID_43921 Human_SNP_ID_189474361 A-to-I Human chr4 - 73057326 73057326 73057326 CATCTCCCGGATTCCAGTGATTTTCCTGCCTCAGCCTCCAAGTATCTGGGATTGCAGGTGCACAC CATCTCCCGGATTCCAGTGATTTTCCTGCCTCTGCCTCCAAGTATCTGGGATTGCAGGTGCACAC T A COX18 Ensembl:ENSG00000163626 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE99789;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;Bronchiolar epithelium,BEP2D cell line - 23474544,24183664,29129909,29796672,30559470,31158229 RNA-Seq:(High) rs1477398836 Functional Loss SNV dbSNP153 33..33 33 - - - 43922 RMVar_ID_43922 Human_SNP_ID_189474472 A-to-I Human chr4 - 73057785 73057785 73057785 GGTGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAACCTGGAATACAGA GGTGCCTGTAATCCCAGCTACTTGGGAGGCTGGGGCAGGAGAATCGCTTGAACCTGGAATACAGA T C COX18 Ensembl:ENSG00000163626 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1220641490 Functional Loss SNV dbSNP153 33..33 33 - - - 43923 RMVar_ID_43923 Human_SNP_ID_189474482 A-to-I Human chr4 - 73057837 73057837 73057837 TGAAACCCTGTCTGTACTAAAATAACAAAAAAATTAGCTGGGCTTAGTGGCAGGTGCCTGTAATC TGAAACCCTGTCTGTACTAAAATAACAAAAAACTTAGCTGGGCTTAGTGGCAGGTGCCTGTAATC T G COX18 Ensembl:ENSG00000163626 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs933209399 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18028958 43924 RMVar_ID_43924 Human_SNP_ID_189474485 A-to-I Human chr4 - 73057849 73057849 73057849 TGGCCAACATGGTGAAACCCTGTCTGTACTAAAATAACAAAAAAATTAGCTGGGCTTAGTGGCAG TGGCCAACATGGTGAAACCCTGTCTGTACTAACATAACAAAAAAATTAGCTGGGCTTAGTGGCAG T G COX18 Ensembl:ENSG00000163626 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs529596293 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18028958 43925 RMVar_ID_43925 Human_SNP_ID_189474489 A-to-I Human chr4 - 73057885 73057881 73057885 GGTGGATCACCTGAGGTCTGGAGTTTGAGACCAGCCTGGCCAACATGGTGAAACCCTGTCTGTAC GGTGGATCACCTGAGGTCTGGAGTTTGAGACC____TGGCCAACATGGTGAAACCCTGTCTGTAC AGGCT A COX18 Ensembl:ENSG00000163626 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1214426240 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_162931 43926 RMVar_ID_43926 Human_SNP_ID_189474493 A-to-I Human chr4 - 73057890 73057890 73057890 AGGTGGGTGGATCACCTGAGGTCTGGAGTTTGAGACCAGCCTGGCCAACATGGTGAAACCCTGTC AGGTGGGTGGATCACCTGAGGTCTGGAGTTTGCGACCAGCCTGGCCAACATGGTGAAACCCTGTC T G COX18 Ensembl:ENSG00000163626 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1342325476 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_162931 43927 RMVar_ID_43927 Human_SNP_ID_189481602 A-to-I Human chr4 - 73085905 73085905 73085905 CTCATTGCAGCCTTAACCTCCTGGGCTCAAGCAATCCTCCCACCTCAGCCTCCCAAGTAACTGGA CTCATTGCAGCCTTAACCTCCTGGGCTCAAGCCATCCTCCCACCTCAGCCTCCCAAGTAACTGGA T G ANKRD17 Ensembl:ENSG00000132466 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1037754475 Functional Loss SNV dbSNP153 33..33 33 - - - 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 43928 RMVar_ID_43928 Human_SNP_ID_189484115 A-to-I Human chr4 - 73094988 73094988 73094988 TGTATTTTTTTCAGTAGAGACAGGATTTCACTATGTTGGCCAGGCTGGTCTCGAACTCCTGACAT TGTATTTTTTTCAGTAGAGACAGGATTTCACTGTGTTGGCCAGGCTGGTCTCGAACTCCTGACAT T C ANKRD17 Ensembl:ENSG00000132466 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs774174968 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28929,RMVar_hsa_circ_123163,RMVar_hsa_circ_102497,RMVar_hsa_circ_226526,RMVar_hsa_circ_226529,RMVar_hsa_circ_69338,RMVar_hsa_circ_78748,RMVar_hsa_circ_226533,RMVar_hsa_circ_226534,RMVar_hsa_circ_8226,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_226537,RMVar_hsa_circ_226535,RMVar_hsa_circ_48962,RMVar_hsa_circ_312455,RMVar_hsa_circ_91835,RMVar_hsa_circ_351377,RMVar_hsa_circ_226542,RMVar_hsa_circ_12774 43929 RMVar_ID_43929 Human_SNP_ID_189484351 A-to-I Human chr4 - 73095909 73095909 73095909 AAGACAAGAGGATCACTTGAGACTATGAGTTCAAGACCAGCCTGGGCAACATAGCAAGACCCCAT AAGACAAGAGGATCACTTGAGACTATGAGTTCTAGACCAGCCTGGGCAACATAGCAAGACCCCAT T A ANKRD17 Ensembl:ENSG00000132466 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs907693168 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28929,RMVar_hsa_circ_123163,RMVar_hsa_circ_102497,RMVar_hsa_circ_226526,RMVar_hsa_circ_226529,RMVar_hsa_circ_69338,RMVar_hsa_circ_78748,RMVar_hsa_circ_226533,RMVar_hsa_circ_226534,RMVar_hsa_circ_8226,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_226537,RMVar_hsa_circ_226535,RMVar_hsa_circ_48962,RMVar_hsa_circ_312455,RMVar_hsa_circ_91835,RMVar_hsa_circ_351377,RMVar_hsa_circ_226542,RMVar_hsa_circ_12774 43930 RMVar_ID_43930 Human_SNP_ID_189484352 A-to-I Human chr4 - 73095909 73095909 73095909 AAGACAAGAGGATCACTTGAGACTATGAGTTCAAGACCAGCCTGGGCAACATAGCAAGACCCCAT AAGACAAGAGGATCACTTGAGACTATGAGTTCGAGACCAGCCTGGGCAACATAGCAAGACCCCAT T C ANKRD17 Ensembl:ENSG00000132466 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs907693168 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28929,RMVar_hsa_circ_123163,RMVar_hsa_circ_102497,RMVar_hsa_circ_226526,RMVar_hsa_circ_226529,RMVar_hsa_circ_69338,RMVar_hsa_circ_78748,RMVar_hsa_circ_226533,RMVar_hsa_circ_226534,RMVar_hsa_circ_8226,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_226537,RMVar_hsa_circ_226535,RMVar_hsa_circ_48962,RMVar_hsa_circ_312455,RMVar_hsa_circ_91835,RMVar_hsa_circ_351377,RMVar_hsa_circ_226542,RMVar_hsa_circ_12774 43931 RMVar_ID_43931 Human_SNP_ID_189484368 A-to-I Human chr4 - 73095965 73095965 73095965 GAATTCGGGCCTGACACCTGTGGCTCATGTCTATAATCCCAGCATTTTGGGAGGCCAAGACAAGA GAATTCGGGCCTGACACCTGTGGCTCATGTCTGTAATCCCAGCATTTTGGGAGGCCAAGACAAGA T C ANKRD17 Ensembl:ENSG00000132466 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs781489944 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28929,RMVar_hsa_circ_123163,RMVar_hsa_circ_102497,RMVar_hsa_circ_226526,RMVar_hsa_circ_226529,RMVar_hsa_circ_69338,RMVar_hsa_circ_78748,RMVar_hsa_circ_226533,RMVar_hsa_circ_226534,RMVar_hsa_circ_8226,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_226537,RMVar_hsa_circ_226535,RMVar_hsa_circ_48962,RMVar_hsa_circ_312455,RMVar_hsa_circ_91835,RMVar_hsa_circ_351377,RMVar_hsa_circ_226542,RMVar_hsa_circ_12774 43932 RMVar_ID_43932 Human_SNP_ID_189486034 A-to-I Human chr4 - 73102102 73102100 73102103 AAAAAAATTTTTTTTAATTATCTGGACACAGTAGCATACTCCTGTAGTCCCAGCTAGCTACTGGG AAAAAAATTTTTTTTAATTATCTGGACACAG___CATACTCCTGTAGTCCCAGCTAGCTACTGGG GCTA G ANKRD17 Ensembl:ENSG00000132466 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277638652 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_10153516,Human_RBP_ID_17574629 RMVar_hsa_circ_28929,RMVar_hsa_circ_123163,RMVar_hsa_circ_102497,RMVar_hsa_circ_226526,RMVar_hsa_circ_226529,RMVar_hsa_circ_78748,RMVar_hsa_circ_226533,RMVar_hsa_circ_226534,RMVar_hsa_circ_8226,RMVar_hsa_circ_309760,RMVar_hsa_circ_365476,RMVar_hsa_circ_375630,RMVar_hsa_circ_53593,RMVar_hsa_circ_226536,RMVar_hsa_circ_226535,RMVar_hsa_circ_48962,RMVar_hsa_circ_91835,RMVar_hsa_circ_351377,RMVar_hsa_circ_26710,RMVar_hsa_circ_72071,RMVar_hsa_circ_226542,RMVar_hsa_circ_12774,RMVar_hsa_circ_330175,RMVar_hsa_circ_226543 43933 RMVar_ID_43933 Human_SNP_ID_189492654 A-to-I Human chr4 - 73130044 73130044 73130044 GAGTAATTAATAGGCAGAGTGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGT GAGTAATTAATAGGCAGAGTGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGT T C ANKRD17 Ensembl:ENSG00000132466 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1358911064 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123163,RMVar_hsa_circ_226526,RMVar_hsa_circ_78748,RMVar_hsa_circ_226533,RMVar_hsa_circ_8226,RMVar_hsa_circ_91835,RMVar_hsa_circ_11946,RMVar_hsa_circ_226542,RMVar_hsa_circ_12774,RMVar_hsa_circ_71851,RMVar_hsa_circ_59145,RMVar_hsa_circ_339787,RMVar_hsa_circ_341602,RMVar_hsa_circ_106505,RMVar_hsa_circ_123838,RMVar_hsa_circ_98806,RMVar_hsa_circ_226545,RMVar_hsa_circ_226544,RMVar_hsa_circ_53224,RMVar_hsa_circ_54510,RMVar_hsa_circ_226551,RMVar_hsa_circ_363535,RMVar_hsa_circ_378655,RMVar_hsa_circ_320863,RMVar_hsa_circ_45419,RMVar_hsa_circ_226555,RMVar_hsa_circ_33782,RMVar_hsa_circ_55413,RMVar_hsa_circ_351972 43934 RMVar_ID_43934 Human_SNP_ID_189500832 A-to-I Human chr4 - 73163720 73163720 73163720 GAAACCTAATTGTTGCTTTTGCAGATATCGCTATAAAGCATGCTTACCCCTAACCTTTTTATTCT GAAACCTAATTGTTGCTTTTGCAGATATCGCTGTAAAGCATGCTTACCCCTAACCTTTTTATTCT T C ANKRD17 Ensembl:ENSG00000132466 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1410844793 Functional Loss SNV dbSNP153 33..33 33 - - - 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 43935 RMVar_ID_43935 Human_SNP_ID_189505967 A-to-I Human chr4 - 73183560 73183560 73183560 CTGAAGGAAGAGAAGGAGGCTGAGGTGGGAGAATCGCTTGAACCCAGGAGGCCAGAGGCTGCAGT CTGAAGGAAGAGAAGGAGGCTGAGGTGGGAGAGTCGCTTGAACCCAGGAGGCCAGAGGCTGCAGT T C ANKRD17 Ensembl:ENSG00000132466 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1163853221 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17574781 RMVar_hsa_circ_91835,RMVar_hsa_circ_226542,RMVar_hsa_circ_115715,RMVar_hsa_circ_226566,RMVar_hsa_circ_226575,RMVar_hsa_circ_226574 43936 RMVar_ID_43936 Human_SNP_ID_189507619 A-to-I Human chr4 - 73190322 73190322 73190322 TCCCATCACCCAGGCTGGGGTGCAGTGGCGCAATCTCAGCTCACTGCAGCCTCTGCCTCCCGGGT TCCCATCACCCAGGCTGGGGTGCAGTGGCGCAGTCTCAGCTCACTGCAGCCTCTGCCTCCCGGGT T C ANKRD17 Ensembl:ENSG00000132466 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs960749546 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91835,RMVar_hsa_circ_226542,RMVar_hsa_circ_115715,RMVar_hsa_circ_226566,RMVar_hsa_circ_226575,RMVar_hsa_circ_226574 43937 RMVar_ID_43937 Human_SNP_ID_189508582 A-to-I Human chr4 - 73193885 73193885 73193885 CTCTGTCACCCAGGCTAGAGTGCAGTGTCGCAATCATGGGTCACTGCAGCCTCAACCTCCTGGGC CTCTGTCACCCAGGCTAGAGTGCAGTGTCGCAGTCATGGGTCACTGCAGCCTCAACCTCCTGGGC T C ANKRD17 Ensembl:ENSG00000132466 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs562489522 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91835,RMVar_hsa_circ_226542,RMVar_hsa_circ_115715,RMVar_hsa_circ_226566,RMVar_hsa_circ_226575 43938 RMVar_ID_43938 Human_SNP_ID_189509119 A-to-I Human chr4 - 73196064 73196064 73196064 GGAGGCAGAGGCTGTAGTGAGCTGAGATTGCCACTGCACTCTAGCCTGGGCTACAGAGTGAGACT GGAGGCAGAGGCTGTAGTGAGCTGAGATTGCCGCTGCACTCTAGCCTGGGCTACAGAGTGAGACT T C ANKRD17 Ensembl:ENSG00000132466 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1431391597 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17574784 RMVar_hsa_circ_91835,RMVar_hsa_circ_226542,RMVar_hsa_circ_115715,RMVar_hsa_circ_226566,RMVar_hsa_circ_226575 43939 RMVar_ID_43939 Human_SNP_ID_189509153 A-to-I Human chr4 - 73196206 73196206 73196206 GTCACGTGAGGTCAGGAGTTTGAGACCAGCCTAACCATCATGGCAAAACCATCTCTACTAAAAAT GTCACGTGAGGTCAGGAGTTTGAGACCAGCCTTACCATCATGGCAAAACCATCTCTACTAAAAAT T A ANKRD17 Ensembl:ENSG00000132466 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1187966435 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91835,RMVar_hsa_circ_226542,RMVar_hsa_circ_115715,RMVar_hsa_circ_226566,RMVar_hsa_circ_226575 43940 RMVar_ID_43940 Human_SNP_ID_189509478 A-to-I Human chr4 - 73197634 73197634 73197634 ATAGAGATGGGTCTTGCTATGTTGCTCAAGCTAGTCTCAAACTTCTGGCCTCAAGTTTATCCTTC ATAGAGATGGGTCTTGCTATGTTGCTCAAGCTGGTCTCAAACTTCTGGCCTCAAGTTTATCCTTC T C ANKRD17 Ensembl:ENSG00000132466 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1220824815 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10153945 RMVar_hsa_circ_91835,RMVar_hsa_circ_226542,RMVar_hsa_circ_115715,RMVar_hsa_circ_226566,RMVar_hsa_circ_226575 43941 RMVar_ID_43941 Human_SNP_ID_189509479 A-to-I Human chr4 - 73197634 73197634 73197634 ATAGAGATGGGTCTTGCTATGTTGCTCAAGCTAGTCTCAAACTTCTGGCCTCAAGTTTATCCTTC ATAGAGATGGGTCTTGCTATGTTGCTCAAGCTCGTCTCAAACTTCTGGCCTCAAGTTTATCCTTC T G ANKRD17 Ensembl:ENSG00000132466 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1220824815 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10153945 RMVar_hsa_circ_91835,RMVar_hsa_circ_226542,RMVar_hsa_circ_115715,RMVar_hsa_circ_226566,RMVar_hsa_circ_226575 43942 RMVar_ID_43942 Human_SNP_ID_189510627 A-to-I Human chr4 - 73202444 73202444 73202444 TAGTTTACAGCTCCTCAATAGTTCTTTTCCCAATTCTCCCTAGTTTTCTGCCCCCACGTTTTAGC TAGTTTACAGCTCCTCAATAGTTCTTTTCCCAGTTCTCCCTAGTTTTCTGCCCCCACGTTTTAGC T C ANKRD17 Ensembl:ENSG00000132466 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1222585417 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7325529,Human_RBP_ID_21899551 RMVar_hsa_circ_91835,RMVar_hsa_circ_226542,RMVar_hsa_circ_115715,RMVar_hsa_circ_226566,RMVar_hsa_circ_226575 43943 RMVar_ID_43943 Human_SNP_ID_189510633 A-to-I Human chr4 - 73202470 73202470 73202470 AATCTTTTGGAGTTTCTATAATTGTTTAGTTTACAGCTCCTCAATAGTTCTTTTCCCAATTCTCC AATCTTTTGGAGTTTCTATAATTGTTTAGTTTCCAGCTCCTCAATAGTTCTTTTCCCAATTCTCC T G ANKRD17 Ensembl:ENSG00000132466 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1268068334 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91835,RMVar_hsa_circ_226542,RMVar_hsa_circ_115715,RMVar_hsa_circ_226566,RMVar_hsa_circ_226575 43944 RMVar_ID_43944 Human_SNP_ID_189513758 A-to-I Human chr4 - 73214745 73214745 73214745 GGAGTCTCAGGCTCCTAAAGCGCTAGCATTACAGGCGTGAGCGACTGCACCTGGCCTAAGATTGA GGAGTCTCAGGCTCCTAAAGCGCTAGCATTACGGGCGTGAGCGACTGCACCTGGCCTAAGATTGA T C ANKRD17 Ensembl:ENSG00000132466 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027942901 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15195364,Human_RBP_ID_17574786,Human_RBP_ID_18029089 RMVar_hsa_circ_91835,RMVar_hsa_circ_226542,RMVar_hsa_circ_115715,RMVar_hsa_circ_226566,RMVar_hsa_circ_226575 43945 RMVar_ID_43945 Human_SNP_ID_189513922 A-to-I Human chr4 - 73215296 73215296 73215296 GAGATAGCACCACTGAACTCAAGCCTGGCGACAGAGCAAGACTCCATCTCAAAAAAAAAAAAATC GAGATAGCACCACTGAACTCAAGCCTGGCGACGGAGCAAGACTCCATCTCAAAAAAAAAAAAATC T C ANKRD17 Ensembl:ENSG00000132466 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs563786200 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15195389,Human_RBP_ID_18032126 RMVar_hsa_circ_91835,RMVar_hsa_circ_226542,RMVar_hsa_circ_115715,RMVar_hsa_circ_226566,RMVar_hsa_circ_226575 43946 RMVar_ID_43946 Human_SNP_ID_189514096 A-to-I Human chr4 - 73215980 73215980 73215980 ATGCACTTTAGCCTTGAACTCCTGGGCTGAGCAGTCATTCTGCCTCAGCCTCCTGAGTAGCTGAG ATGCACTTTAGCCTTGAACTCCTGGGCTGAGCGGTCATTCTGCCTCAGCCTCCTGAGTAGCTGAG T C ANKRD17 Ensembl:ENSG00000132466 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1485015941 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_623917,Human_RBP_ID_7325714 RMVar_hsa_circ_91835,RMVar_hsa_circ_226542,RMVar_hsa_circ_115715,RMVar_hsa_circ_226566,RMVar_hsa_circ_226575 43947 RMVar_ID_43947 Human_SNP_ID_189516082 A-to-I Human chr4 - 73224190 73224190 73224190 GCCCAGGCTAGGGTGCCAGTGGCACAATGGCAACATCCACCTCCCGGGTTCACGTGATTCTCATG GCCCAGGCTAGGGTGCCAGTGGCACAATGGCAGCATCCACCTCCCGGGTTCACGTGATTCTCATG T C ANKRD17 Ensembl:ENSG00000132466 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs933808669 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10165650,Human_RBP_ID_25835534 RMVar_hsa_circ_91835,RMVar_hsa_circ_226542,RMVar_hsa_circ_115715,RMVar_hsa_circ_226566,RMVar_hsa_circ_226575,RMVar_hsa_circ_226577 43948 RMVar_ID_43948 Human_SNP_ID_189516427 A-to-I Human chr4 - 73225754 73225754 73225754 GGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCGCCCACCACTACA GGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCGCCCACCACTACA T C ANKRD17 Ensembl:ENSG00000132466 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs981029647 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91835,RMVar_hsa_circ_226542,RMVar_hsa_circ_115715,RMVar_hsa_circ_226566,RMVar_hsa_circ_226575,RMVar_hsa_circ_226577 43949 RMVar_ID_43949 Human_SNP_ID_189516594 A-to-I Human chr4 - 73226104 73226104 73226104 GGGCGTGGTGGCACGCGCCTGTAGTCCCAGCTACTCGGGAAGCTGAGGCAGGAGAATTGCTTGAA GGGCGTGGTGGCACGCGCCTGTAGTCCCAGCTGCTCGGGAAGCTGAGGCAGGAGAATTGCTTGAA T C ANKRD17 Ensembl:ENSG00000132466 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1180779554 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91835,RMVar_hsa_circ_226542,RMVar_hsa_circ_115715,RMVar_hsa_circ_226566,RMVar_hsa_circ_226575,RMVar_hsa_circ_226577 43950 RMVar_ID_43950 Human_SNP_ID_189519934 A-to-I Human chr4 - 73240431 73240431 73240431 TTTTTGTAGAGATAGTCTTGCTGTGTTGCCCAAGTTATTCTAGAACTCCTGGGCTCAGGTGATCC TTTTTGTAGAGATAGTCTTGCTGTGTTGCCCAGGTTATTCTAGAACTCCTGGGCTCAGGTGATCC T C ANKRD17 Ensembl:ENSG00000132466 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017565462 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15196367 RMVar_hsa_circ_91835,RMVar_hsa_circ_226542,RMVar_hsa_circ_115715,RMVar_hsa_circ_226566 43951 RMVar_ID_43951 Human_SNP_ID_189666507 A-to-I Human chr4 + 73804997 73804985 73804997 AGTCCCAGCTGCTTGGGAGGCTGGGGCGGGAGAATCGCTTGAACCCTGGAGGCAGAGGTTGCAAT AGTCCCAGCTGCTTGGGAGGC____________ATCGCTTGAACCCTGGAGGCAGAGGTTGCAAT CTGGGGCGGGAGA C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1299921013 Functional Loss DEL dbSNP153 22..33 33 - - - 43952 RMVar_ID_43952 Human_SNP_ID_189666514 A-to-I Human chr4 + 73804997 73804996 73804997 AGTCCCAGCTGCTTGGGAGGCTGGGGCGGGAGAATCGCTTGAACCCTGGAGGCAGAGGTTGCAAT AGTCCCAGCTGCTTGGGAGGCTGGGGCGGGAG_ATCGCTTGAACCCTGGAGGCAGAGGTTGCAAT GA G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569118900 Functional Loss DEL dbSNP153 33..33 33 - - - 43953 RMVar_ID_43953 Human_SNP_ID_189740949 A-to-I Human chr4 - 74086292 74086292 74086292 ATTGAATTAGACCAAGTTAAGCAACAACTAATACATGAAACCAGTTGAATCAGAGCAAATAATAA ATTGAATTAGACCAAGTTAAGCAACAACTAATGCATGAAACCAGTTGAATCAGAGCAAATAATAA T C AC093677.1 Ensembl:ENSG00000251017 Pseudogene exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs879110657 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1896716 43954 RMVar_ID_43954 Human_SNP_ID_189798150 A-to-I Human chr4 + 74318770 74318770 74318770 CTTCTGACTCAGCCTCTTGAGTAGCTGGGACTACAGGTGTGTGCCACCACACCCAGCTAATTTTT CTTCTGACTCAGCCTCTTGAGTAGCTGGGACTGCAGGTGTGTGCCACCACACCCAGCTAATTTTT A G lnc-EPGN-1 RNACentral:URS00008B5D0A lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913613001 Functional Loss SNV dbSNP153 33..33 33 - - - 43955 RMVar_ID_43955 Human_SNP_ID_189816132 A-to-I Human chr4 + 74385967 74385967 74385967 GGTGTATTTTTCCAAATGAAAAATCTCAATTGAAAGCTTTTAAAATGTAGAAACTTAAACACACC GGTGTATTTTTCCAAATGAAAAATCTCAATTGGAAGCTTTTAAAATGTAGAAACTTAAACACACC A G EREG Ensembl:ENSG00000124882 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1273785925 Functional Loss SNV dbSNP153 33..33 33 - - - 43956 RMVar_ID_43956 Human_SNP_ID_575627155 A-to-I Human chr15 + 45046274 45046274 45046274 ATAGACATTTTATTTTTTCGAGATGAAGTCTCATTCTGTTGTCCAGGCTGGAGTGTAGTGGTGCC ATAGACATTTTATTTTTTCGAGATGAAGTCTCTTTCTGTTGTCCAGGCTGGAGTGTAGTGGTGCC A T SORD Ensembl:ENSG00000140263 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1364172989 Functional Loss SNV dbSNP153 33..33 33 - - - 43957 RMVar_ID_43957 Human_SNP_ID_575737876 A-to-I Human chr15 - 45482884 45482884 45482884 CTTGTAAGGCTGTGGCAGAAGTGCTTTAGCCCAGGAGGTTGAGGCTGCAGTGAGCCATGTCCACA CTTGTAAGGCTGTGGCAGAAGTGCTTTAGCCCGGGAGGTTGAGGCTGCAGTGAGCCATGTCCACA T C SLC30A4 Ensembl:ENSG00000104154 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1162227374 Functional Loss SNV dbSNP153 33..33 33 - - - 43958 RMVar_ID_43958 Human_SNP_ID_575737897 A-to-I Human chr15 - 45483010 45483010 45483010 GGAGGCAAAGGTGGAAGTATCCCTCGAGGCCAAGAGTTCATGACCAGCCTGGTCTTTTGTAGAGA GGAGGCAAAGGTGGAAGTATCCCTCGAGGCCAGGAGTTCATGACCAGCCTGGTCTTTTGTAGAGA T C SLC30A4 Ensembl:ENSG00000104154 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1419082172 Functional Loss SNV dbSNP153 33..33 33 - - - 43959 RMVar_ID_43959 Human_SNP_ID_575742296 A-to-I Human chr15 - 45502773 45502773 45502773 CCAGGCTGGTCCTGAACTCCTAGCTTCAAGCTATCCTTCCACCTCAGTCTCCCAAAGTGCTGGGA CCAGGCTGGTCCTGAACTCCTAGCTTCAAGCTGTCCTTCCACCTCAGTCTCCCAAAGTGCTGGGA T C SLC30A4 Ensembl:ENSG00000104154 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971630020 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_322871,RMVar_hsa_circ_171718,RMVar_hsa_circ_171719,RMVar_hsa_circ_282878,RMVar_hsa_circ_19096,RMVar_hsa_circ_362382,RMVar_hsa_circ_171721 43960 RMVar_ID_43960 Human_SNP_ID_575745131 A-to-I Human chr15 + 45515771 45515771 45515771 AATTTCTTTTCTTTTTTTTTTTTCTTTGAGATAGAGTCTCACTCTGTCACCCAGGCTGGAGAGCA AATTTCTTTTCTTTTTTTTTTTTCTTTGAGATTGAGTCTCACTCTGTCACCCAGGCTGGAGAGCA A T HMGN2P46 Ensembl:ENSG00000179362 Pseudogene intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1209338353 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1597492 43961 RMVar_ID_43961 Human_SNP_ID_575745185 A-to-I Human chr15 + 45516033 45516033 45516033 TTGTTCCTCCTGCCTCAGCCTCCCAAAGTGCTAGGACTACAGGCATGAGCTACTGCGCCCACCCT TTGTTCCTCCTGCCTCAGCCTCCCAAAGTGCTGGGACTACAGGCATGAGCTACTGCGCCCACCCT A G HMGN2P46 Ensembl:ENSG00000179362 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1176882521 Functional Loss SNV dbSNP153 33..33 33 - - - 43962 RMVar_ID_43962 Human_SNP_ID_575746038 A-to-I Human chr15 + 45519418 45519418 45519418 CCATGACGCCTGGCTAATTTTTTTGTATTTTCAGTAGAGACGGGGTTTCACCATGTTGGCCAGTC CCATGACGCCTGGCTAATTTTTTTGTATTTTCCGTAGAGACGGGGTTTCACCATGTTGGCCAGTC A C HMGN2P46 Ensembl:ENSG00000179362 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs186403282 Functional Loss SNV dbSNP153 33..33 33 - - - 43963 RMVar_ID_43963 Human_SNP_ID_575764660 A-to-I Human chr15 + 45600580 45600580 45600580 CAATTGATAGGACCATGTAATTTTTCTTCTTTAGCCTGTTGATGTGGTAGATTACATTGATTGAA CAATTGATAGGACCATGTAATTTTTCTTCTTTGGCCTGTTGATGTGGTAGATTACATTGATTGAA A G AC090527.3,BLOC1S6 Ensembl:ENSG00000260170,Ensembl:ENSG00000104164 Protein coding,Protein coding intron,intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1306423111 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_458188,Human_RBP_ID_12519176 43964 RMVar_ID_43964 Human_SNP_ID_575777561 A-to-I Human chr15 + 45652148 45652148 45652148 TGCCCACCTTGGCCTCCTGAGGTGCTGGGATTACAGGCGTGAGCCACCACGTCCGGCCGGTAGTT TGCCCACCTTGGCCTCCTGAGGTGCTGGGATTTCAGGCGTGAGCCACCACGTCCGGCCGGTAGTT A T AC090527.3,SQOR Ensembl:ENSG00000260170,Ensembl:ENSG00000137767 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs539955326 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_171723,RMVar_hsa_circ_127194 43965 RMVar_ID_43965 Human_SNP_ID_575783841 A-to-I Human chr15 + 45676289 45676289 45676289 CAAGAGGCTGTATTTGAGAACCTGGACAAACCAGGAGAGACCCAAGTGATTTCAGTGAGTGGTGA CAAGAGGCTGTATTTGAGAACCTGGACAAACCGGGAGAGACCCAAGTGATTTCAGTGAGTGGTGA A G AC090527.3,SQOR Ensembl:ENSG00000260170,Ensembl:ENSG00000137767 Protein coding,Protein coding CDS,CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1220196078 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_19068124 Human_Splice_Rec_1597657,Human_Splice_Rec_1597687 Human_miRNA_ID_2479364 RMVar_hsa_circ_103953,RMVar_hsa_circ_171723,RMVar_hsa_circ_127194,RMVar_hsa_circ_304282,RMVar_hsa_circ_75369,RMVar_hsa_circ_362762,RMVar_hsa_circ_171724,RMVar_hsa_circ_355116,RMVar_hsa_circ_75327,RMVar_hsa_circ_171725,RMVar_hsa_circ_344736,RMVar_hsa_circ_54854 43966 RMVar_ID_43966 Human_SNP_ID_575783842 A-to-I Human chr15 + 45676289 45676289 45676289 CAAGAGGCTGTATTTGAGAACCTGGACAAACCAGGAGAGACCCAAGTGATTTCAGTGAGTGGTGA CAAGAGGCTGTATTTGAGAACCTGGACAAACCCGGAGAGACCCAAGTGATTTCAGTGAGTGGTGA A C AC090527.3,SQOR Ensembl:ENSG00000260170,Ensembl:ENSG00000137767 Protein coding,Protein coding CDS,CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) - Functional Loss SNV HGVD 33..33 33 - - - Human_RBP_ID_19068124 Human_Splice_Rec_1597657,Human_Splice_Rec_1597687 Human_miRNA_ID_2479364 RMVar_hsa_circ_103953,RMVar_hsa_circ_171723,RMVar_hsa_circ_127194,RMVar_hsa_circ_304282,RMVar_hsa_circ_75369,RMVar_hsa_circ_362762,RMVar_hsa_circ_171724,RMVar_hsa_circ_355116,RMVar_hsa_circ_75327,RMVar_hsa_circ_171725,RMVar_hsa_circ_344736,RMVar_hsa_circ_54854 43967 RMVar_ID_43967 Human_SNP_ID_576445230 A-to-I Human chr15 - 48328918 48328913 48328918 CCTGGGCAACGTAGGCAGACCCCATCTCTACAAAACATATACAAAATTAGCCAGGCATGGTGGGT CCTGGGCAACGTAGGCAGACCCCATCTCTACA_____TATACAAAATTAGCCAGGCATGGTGGGT ATGTTT A AC023355.2 Ensembl:ENSG00000259488 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs753363153 Functional Loss DEL dbSNP153 33..37 33 - - - 43968 RMVar_ID_43968 Human_SNP_ID_576608560 A-to-I Human chr15 - 49010662 49010662 49010662 ACAAAAAAATACAAGAATTAACTGGGCATGGTAGCTCATATTTATAGTCCAAGCTACTTGGGGGA ACAAAAAAATACAAGAATTAACTGGGCATGGTGGCTCATATTTATAGTCCAAGCTACTTGGGGGA T C SECISBP2L Ensembl:ENSG00000138593 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1368474597 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43334,RMVar_hsa_circ_171821,RMVar_hsa_circ_307198,RMVar_hsa_circ_268994,RMVar_hsa_circ_369705,RMVar_hsa_circ_73281,RMVar_hsa_circ_62849,RMVar_hsa_circ_13933,RMVar_hsa_circ_345508,RMVar_hsa_circ_171822,RMVar_hsa_circ_342321,RMVar_hsa_circ_171824,RMVar_hsa_circ_61617 43969 RMVar_ID_43969 Human_SNP_ID_576608590 A-to-I Human chr15 - 49010787 49010787 49010787 TACACGTGGGCTGGGCGCAGTGGCTCACGCCTATAATCCCAACACTTTGGTAAGCCAAGATGGGC TACACGTGGGCTGGGCGCAGTGGCTCACGCCTGTAATCCCAACACTTTGGTAAGCCAAGATGGGC T C SECISBP2L Ensembl:ENSG00000138593 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1368983857 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43334,RMVar_hsa_circ_171821,RMVar_hsa_circ_307198,RMVar_hsa_circ_268994,RMVar_hsa_circ_369705,RMVar_hsa_circ_73281,RMVar_hsa_circ_62849,RMVar_hsa_circ_13933,RMVar_hsa_circ_345508,RMVar_hsa_circ_171822,RMVar_hsa_circ_342321,RMVar_hsa_circ_171824,RMVar_hsa_circ_61617 43970 RMVar_ID_43970 Human_SNP_ID_576665684 A-to-I Human chr15 + 49244142 49244142 49244142 ATTATTATTAAAAATAGAGTTGGGGCCTCTCTATGTTGCCCAGGCTGGTCTCAAACTCCTGACCT ATTATTATTAAAAATAGAGTTGGGGCCTCTCTGTGTTGCCCAGGCTGGTCTCAAACTCCTGACCT A G GALK2 Ensembl:ENSG00000156958 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs888420820 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56005,RMVar_hsa_circ_34318,RMVar_hsa_circ_374531,RMVar_hsa_circ_73701,RMVar_hsa_circ_171837,RMVar_hsa_circ_366854,RMVar_hsa_circ_74036,RMVar_hsa_circ_275625,RMVar_hsa_circ_290466,RMVar_hsa_circ_66835,RMVar_hsa_circ_171843,RMVar_hsa_circ_97978,RMVar_hsa_circ_281144,RMVar_hsa_circ_171840,RMVar_hsa_circ_171841,RMVar_hsa_circ_171842,RMVar_hsa_circ_350166,RMVar_hsa_circ_285715,RMVar_hsa_circ_272074,RMVar_hsa_circ_270225,RMVar_hsa_circ_171845,RMVar_hsa_circ_171847,RMVar_hsa_circ_171848,RMVar_hsa_circ_171846,RMVar_hsa_circ_171844,RMVar_hsa_circ_367768 43971 RMVar_ID_43971 Human_SNP_ID_576694320 A-to-I Human chr15 - 49365733 49365733 49365733 CAAAATGAAGACAGGTGGGCTTGGATTTTACAAGATATCTTGGAGATTGCTTTCTGTCTGAATTT CAAAATGAAGACAGGTGGGCTTGGATTTTACAGGATATCTTGGAGATTGCTTTCTGTCTGAATTT T C FAM227B,AC022306.1 Ensembl:ENSG00000166262,Ensembl:ENSG00000259531 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs902368568 Functional Loss SNV dbSNP153 33..33 33 - - - 43972 RMVar_ID_43972 Human_SNP_ID_576762181 A-to-I Human chr15 + 49648482 49648482 49648482 TGCCACCACACCCCGCTAATTTTTGTATTTTTAGTAGAGATGGAGTTTTGTCATGTTTGGCCAGC TGCCACCACACCCCGCTAATTTTTGTATTTTTGGTAGAGATGGAGTTTTGTCATGTTTGGCCAGC A G DTWD1 Ensembl:ENSG00000104047 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1345506887 Functional Loss SNV dbSNP153 33..33 33 - - - 43973 RMVar_ID_43973 Human_SNP_ID_576924731 A-to-I Human chr15 - 50323789 50323789 50323789 TGGCTCACTGAAGCCTCAAACTTCTGGGCTTAAGCGATCCTCCCGCCCCAGCCTCCTGAGTAGCT TGGCTCACTGAAGCCTCAAACTTCTGGGCTTATGCGATCCTCCCGCCCCAGCCTCCTGAGTAGCT T A GABPB1 Ensembl:ENSG00000104064 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1208015379 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29802,RMVar_hsa_circ_81405,RMVar_hsa_circ_171877,RMVar_hsa_circ_122669,RMVar_hsa_circ_171892 43974 RMVar_ID_43974 Human_SNP_ID_576924805 A-to-I Human chr15 - 50324170 50324170 50324170 AGATGAGGTCTTATTCTGTAGTCTAGACTGGAATGCAGTGGTGCAATCACAGCTCACTGCAGCCT AGATGAGGTCTTATTCTGTAGTCTAGACTGGACTGCAGTGGTGCAATCACAGCTCACTGCAGCCT T G GABPB1 Ensembl:ENSG00000104064 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs926059652 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29802,RMVar_hsa_circ_81405,RMVar_hsa_circ_171877,RMVar_hsa_circ_122669,RMVar_hsa_circ_171892 43975 RMVar_ID_43975 Human_SNP_ID_576928460 A-to-I Human chr15 - 50338612 50338612 50338612 AAAATTAGTTGGGCATGGTGGTGTTTGCCTGTAGCCCCAGCTACTCGGGAGGCTGAGGTGGGAGG AAAATTAGTTGGGCATGGTGGTGTTTGCCTGTCGCCCCAGCTACTCGGGAGGCTGAGGTGGGAGG T G GABPB1 Ensembl:ENSG00000104064 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1230497718 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29802,RMVar_hsa_circ_81405,RMVar_hsa_circ_171877,RMVar_hsa_circ_122669,RMVar_hsa_circ_171892 43976 RMVar_ID_43976 Human_SNP_ID_576931857 A-to-I Human chr15 - 50351454 50351454 50351454 CCTCTGCCTCAGCCTCCTGAGTAGTTGGGACTACAGGTACCTGCCAACATGTCTGGCTAATTTTT CCTCTGCCTCAGCCTCCTGAGTAGTTGGGACTGCAGGTACCTGCCAACATGTCTGGCTAATTTTT T C GABPB1-IT1,GABPB1 Ensembl:ENSG00000285410,Ensembl:ENSG00000104064 lincRNA,Protein coding exon,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs749953050 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81405,RMVar_hsa_circ_171877 43977 RMVar_ID_43977 Human_SNP_ID_576933933 A-to-I Human chr15 + 50357484 50357484 50357484 GGGAGGCCGAGGTGGGTGGATCTCCTGAGTTCAGGAGTTAAAGAGCAGCCTGGCCAACATGGCAA GGGAGGCCGAGGTGGGTGGATCTCCTGAGTTCGGGAGTTAAAGAGCAGCCTGGCCAACATGGCAA A G GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA exon GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1411688051 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3489887,Human_RBP_ID_5087779,Human_RBP_ID_9816704,Human_RBP_ID_22929103,Human_RBP_ID_25185722 43978 RMVar_ID_43978 Human_SNP_ID_576933955 A-to-I Human chr15 + 50357568 50357568 50357568 AAAATTAGCTGGGCATGGTGGCACGCTCCTGTAATTCCAGCTACTCCGGAGGCTGAGGCAGGAGA AAAATTAGCTGGGCATGGTGGCACGCTCCTGTCATTCCAGCTACTCCGGAGGCTGAGGCAGGAGA A C GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1321587304 Functional Loss SNV dbSNP153 33..33 33 - - - 43979 RMVar_ID_43979 Human_SNP_ID_576933958 A-to-I Human chr15 + 50357578 50357578 50357578 GGGCATGGTGGCACGCTCCTGTAATTCCAGCTACTCCGGAGGCTGAGGCAGGAGAGTAGCTTGAA GGGCATGGTGGCACGCTCCTGTAATTCCAGCTGCTCCGGAGGCTGAGGCAGGAGAGTAGCTTGAA A G GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1175955562 Functional Loss SNV dbSNP153 33..33 33 - - - 43980 RMVar_ID_43980 Human_SNP_ID_576933975 A-to-I Human chr15 + 50357630 50357630 50357630 AGAGTAGCTTGAACCCAGGACACGGAGGCTGCAGTGAGCCGAGATTGCGCCACTGCACTCCAGCC AGAGTAGCTTGAACCCAGGACACGGAGGCTGCGGTGAGCCGAGATTGCGCCACTGCACTCCAGCC A G GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1190373742 Functional Loss SNV dbSNP153 33..33 33 - - - 43981 RMVar_ID_43981 Human_SNP_ID_576934569 A-to-I Human chr15 + 50359558 50359552 50359558 TTCATTGCCTGACCTTGTGATCCGCCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTAAG TTCATTGCCTGACCTTGTGATCCGCCT______GCCTCCCAAAGTGCTGGGATTACAGGCGTAAG TGCCTCA T GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1392890717 Functional Loss DEL dbSNP153 28..33 33 - - - 43982 RMVar_ID_43982 Human_SNP_ID_576934637 A-to-I Human chr15 + 50359735 50359735 50359735 ACCTCTGCCTCCTGAGTTGAAGCGATACTCCTACCTCAGCCTCCCAAGTAGCTGGGATTACAAGC ACCTCTGCCTCCTGAGTTGAAGCGATACTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAAGC A G GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1227612126 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8251753 43983 RMVar_ID_43983 Human_SNP_ID_576934643 A-to-I Human chr15 + 50359748 50359748 50359748 GAGTTGAAGCGATACTCCTACCTCAGCCTCCCAAGTAGCTGGGATTACAAGCATGCACCACCATA GAGTTGAAGCGATACTCCTACCTCAGCCTCCCGAGTAGCTGGGATTACAAGCATGCACCACCATA A G GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1213300162 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8251753 43984 RMVar_ID_43984 Human_SNP_ID_576934885 A-to-I Human chr15 + 50360646 50360646 50360646 CAGGCTGGAAGGCCGTGATGTGATCTCAGCTCACTGCAGCCTCAACCTGGGCTCAAGCGATCCTC CAGGCTGGAAGGCCGTGATGTGATCTCAGCTCGCTGCAGCCTCAACCTGGGCTCAAGCGATCCTC A G GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs111718108 Functional Loss SNV dbSNP153 33..33 33 - - - 43985 RMVar_ID_43985 Human_SNP_ID_576934894 A-to-I Human chr15 + 50360698 50360698 50360698 TCAAGCGATCCTCCCACCTCAGCCTCCTGAGTAGCTGGGACTACAGGTGCACACCACCACGCCCA TCAAGCGATCCTCCCACCTCAGCCTCCTGAGTGGCTGGGACTACAGGTGCACACCACCACGCCCA A G GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1209792093 Functional Loss SNV dbSNP153 33..33 33 - - - 43986 RMVar_ID_43986 Human_SNP_ID_576934897 A-to-I Human chr15 + 50360708 50360708 50360708 CTCCCACCTCAGCCTCCTGAGTAGCTGGGACTACAGGTGCACACCACCACGCCCAGCTCATTTTT CTCCCACCTCAGCCTCCTGAGTAGCTGGGACTGCAGGTGCACACCACCACGCCCAGCTCATTTTT A G GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs944917287 Functional Loss SNV dbSNP153 33..33 33 - - - 43987 RMVar_ID_43987 Human_SNP_ID_576934911 A-to-I Human chr15 + 50360783 50360783 50360783 TAGAGACTGTGTTTTGCCACGTTGCCCAGGCTATTCTCAAACTCCTGAGCTCAAGTGATCCTCCC TAGAGACTGTGTTTTGCCACGTTGCCCAGGCTTTTCTCAAACTCCTGAGCTCAAGTGATCCTCCC A T GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1421706709 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17563191 43988 RMVar_ID_43988 Human_SNP_ID_576935616 A-to-I Human chr15 + 50363404 50363404 50363404 GCTTGAATGAAGAATAGCTTTTTTTTTCTCTGAGACACGGTCTTACTCTGTTGCCCAAGCTGGCG GCTTGAATGAAGAATAGCTTTTTTTTTCTCTGTGACACGGTCTTACTCTGTTGCCCAAGCTGGCG A T GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1209665766 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2443489,Human_RBP_ID_12523619 43989 RMVar_ID_43989 Human_SNP_ID_576935648 A-to-I Human chr15 + 50363520 50363520 50363520 GATTCTCCCACCTCAGCCTCCTTAGCAGCTAGAACTACAAGCGCAGCCACCATGCCTGGCTAATT GATTCTCCCACCTCAGCCTCCTTAGCAGCTAGGACTACAAGCGCAGCCACCATGCCTGGCTAATT A G GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1360529372 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3490365,Human_RBP_ID_5247046,Human_RBP_ID_17563193 43990 RMVar_ID_43990 Human_SNP_ID_576935650 A-to-I Human chr15 + 50363524 50363524 50363524 CTCCCACCTCAGCCTCCTTAGCAGCTAGAACTACAAGCGCAGCCACCATGCCTGGCTAATTCTGT CTCCCACCTCAGCCTCCTTAGCAGCTAGAACTGCAAGCGCAGCCACCATGCCTGGCTAATTCTGT A G GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1349325904 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3490365,Human_RBP_ID_5247046,Human_RBP_ID_17563193 43991 RMVar_ID_43991 Human_SNP_ID_576935663 A-to-I Human chr15 + 50363585 50363585 50363585 CTGTGTATTTCTGGTAGAGATGGGGTTTTGCCATGTTGCCCAGGCTAGTCTTGAACTCCTGAGCT CTGTGTATTTCTGGTAGAGATGGGGTTTTGCCGTGTTGCCCAGGCTAGTCTTGAACTCCTGAGCT A G GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1245835274 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3490365,Human_RBP_ID_5247046 43992 RMVar_ID_43992 Human_SNP_ID_576935667 A-to-I Human chr15 + 50363599 50363599 50363599 TAGAGATGGGGTTTTGCCATGTTGCCCAGGCTAGTCTTGAACTCCTGAGCTCAAGCGAGACACCC TAGAGATGGGGTTTTGCCATGTTGCCCAGGCTGGTCTTGAACTCCTGAGCTCAAGCGAGACACCC A G GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1313821614 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5247046,Human_RBP_ID_25143603 43993 RMVar_ID_43993 Human_SNP_ID_576935677 A-to-I Human chr15 + 50363632 50363632 50363632 GTCTTGAACTCCTGAGCTCAAGCGAGACACCCACCTTGACCTCCCAAAGTGTTGGGATTACAGAC GTCTTGAACTCCTGAGCTCAAGCGAGACACCCGCCTTGACCTCCCAAAGTGTTGGGATTACAGAC A G GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941997290 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5247046 43994 RMVar_ID_43994 Human_SNP_ID_576935977 A-to-I Human chr15 + 50364710 50364710 50364710 TTGGGTCACTGCAACCTCCGTCTCCCGAGTTCAAGCAATTCTCCTGCCTCAGCCTCCCATGTAGC TTGGGTCACTGCAACCTCCGTCTCCCGAGTTCCAGCAATTCTCCTGCCTCAGCCTCCCATGTAGC A C GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs180979039 Functional Loss SNV dbSNP153 33..33 33 - - - 43995 RMVar_ID_43995 Human_SNP_ID_576935978 A-to-I Human chr15 + 50364714 50364714 50364714 GTCACTGCAACCTCCGTCTCCCGAGTTCAAGCAATTCTCCTGCCTCAGCCTCCCATGTAGCTGGG GTCACTGCAACCTCCGTCTCCCGAGTTCAAGCGATTCTCCTGCCTCAGCCTCCCATGTAGCTGGG A G GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1482501545 Functional Loss SNV dbSNP153 33..33 33 - - - 43996 RMVar_ID_43996 Human_SNP_ID_576936243 A-to-I Human chr15 + 50365754 50365754 50365754 TTTGACCAACCTGGGCAATAGAGCAAAATCCCATCTCTACAAAAAAATACAAAAATTAGTCGGGC TTTGACCAACCTGGGCAATAGAGCAAAATCCCGTCTCTACAAAAAAATACAAAAATTAGTCGGGC A G GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1567572020 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_760022,Human_RBP_ID_3490367 43997 RMVar_ID_43997 Human_SNP_ID_576936245 A-to-I Human chr15 + 50365767 50365758 50365768 GGCAATAGAGCAAAATCCCATCTCTACAAAAAAATACAAAAATTAGTCGGGCATGGTGGTGCTGC GGCAATAGAGCAAAATCCCATCTC__________TACAAAAATTAGTCGGGCATGGTGGTGCTGC CTACAAAAAAA C GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs577535815 Functional Loss DEL dbSNP153 25..34 33 - - - Human_RBP_ID_3490367 43998 RMVar_ID_43998 Human_SNP_ID_576936246 A-to-I Human chr15 + 50365760 50365760 50365760 CAACCTGGGCAATAGAGCAAAATCCCATCTCTACAAAAAAATACAAAAATTAGTCGGGCATGGTG CAACCTGGGCAATAGAGCAAAATCCCATCTCTGCAAAAAAATACAAAAATTAGTCGGGCATGGTG A G GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs886124565 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3490367 43999 RMVar_ID_43999 Human_SNP_ID_576936249 A-to-I Human chr15 + 50365767 50365767 50365767 GGCAATAGAGCAAAATCCCATCTCTACAAAAAAATACAAAAATTAGTCGGGCATGGTGGTGCTGC GGCAATAGAGCAAAATCCCATCTCTACAAAAAGATACAAAAATTAGTCGGGCATGGTGGTGCTGC A G GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1567572023 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3490367 44000 RMVar_ID_44000 Human_SNP_ID_576936250 A-to-I Human chr15 + 50365770 50365770 50365770 AATAGAGCAAAATCCCATCTCTACAAAAAAATACAAAAATTAGTCGGGCATGGTGGTGCTGCCTG AATAGAGCAAAATCCCATCTCTACAAAAAAATTCAAAAATTAGTCGGGCATGGTGGTGCTGCCTG A T GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1257176872 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3490367 44001 RMVar_ID_44001 Human_SNP_ID_576936271 A-to-I Human chr15 + 50365814 50365814 50365814 CGGGCATGGTGGTGCTGCCTGTAGTGACGGCTACTCATCCTGAGGTGGGAAGATTGCTTGAGGCC CGGGCATGGTGGTGCTGCCTGTAGTGACGGCTCCTCATCCTGAGGTGGGAAGATTGCTTGAGGCC A C GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs956056428 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3490367 44002 RMVar_ID_44002 Human_SNP_ID_576936272 A-to-I Human chr15 + 50365814 50365814 50365814 CGGGCATGGTGGTGCTGCCTGTAGTGACGGCTACTCATCCTGAGGTGGGAAGATTGCTTGAGGCC CGGGCATGGTGGTGCTGCCTGTAGTGACGGCTGCTCATCCTGAGGTGGGAAGATTGCTTGAGGCC A G GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs956056428 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3490367 44003 RMVar_ID_44003 Human_SNP_ID_576936283 A-to-I Human chr15 + 50365847 50365847 50365847 CTCATCCTGAGGTGGGAAGATTGCTTGAGGCCAGGAGGTTGAGGCTGCAGTGAGCCAGGATCACA CTCATCCTGAGGTGGGAAGATTGCTTGAGGCCTGGAGGTTGAGGCTGCAGTGAGCCAGGATCACA A T GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs1015668835 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9053137 44004 RMVar_ID_44004 Human_SNP_ID_576936451 A-to-I Human chr15 + 50366427 50366427 50366427 GTGACTATACCCCTTTTTTGAGTCAGAGTCTCACTACGTTACCCAGGCTGGAGTACAGTGGTACG GTGACTATACCCCTTTTTTGAGTCAGAGTCTCGCTACGTTACCCAGGCTGGAGTACAGTGGTACG A G GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs906053806 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_3207443,Human_miRNA_ID_3209352 44005 RMVar_ID_44005 Human_SNP_ID_576936475 A-to-I Human chr15 + 50366535 50366535 50366535 CTCCAGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCGCCTACCACCACACCTGGCTAATTTTT CTCCAGCCTCAGCCTCCCAAGTAGCTGGGATTGCAGGCGCCTACCACCACACCTGGCTAATTTTT A G GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1304328330 Functional Loss SNV dbSNP153 33..33 33 - - - 44006 RMVar_ID_44006 Human_SNP_ID_576936488 A-to-I Human chr15 + 50366596 50366596 50366596 TTTTGTATTTTTAGTAGAGATGGGGTTTTACCATGTTGGCCAGGCTGGCCTCAAACTCTGGACTT TTTTGTATTTTTAGTAGAGATGGGGTTTTACCGTGTTGGCCAGGCTGGCCTCAAACTCTGGACTT A G GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1019955898 Functional Loss SNV dbSNP153 33..33 33 - - - 44007 RMVar_ID_44007 Human_SNP_ID_576936489 A-to-I Human chr15 + 50366596 50366596 50366596 TTTTGTATTTTTAGTAGAGATGGGGTTTTACCATGTTGGCCAGGCTGGCCTCAAACTCTGGACTT TTTTGTATTTTTAGTAGAGATGGGGTTTTACCTTGTTGGCCAGGCTGGCCTCAAACTCTGGACTT A T GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1019955898 Functional Loss SNV dbSNP153 33..33 33 - - - 44008 RMVar_ID_44008 Human_SNP_ID_576936537 A-to-I Human chr15 + 50366812 50366812 50366812 ACCCCAGCTGGAGTACAGTGGCACAGTATCACAGCTTGCTGCAGCATCAAATTCCTAGGCTCAAG ACCCCAGCTGGAGTACAGTGGCACAGTATCACGGCTTGCTGCAGCATCAAATTCCTAGGCTCAAG A G GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs3178999 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5247051 44009 RMVar_ID_44009 Human_SNP_ID_576936542 A-to-I Human chr15 + 50366836 50366836 50366836 AGTATCACAGCTTGCTGCAGCATCAAATTCCTAGGCTCAAGCCATCCTTCCACCGGACATGTTGG AGTATCACAGCTTGCTGCAGCATCAAATTCCTGGGCTCAAGCCATCCTTCCACCGGACATGTTGG A G GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs3179000 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5247051,Human_RBP_ID_8251726,Human_RBP_ID_23161765 44010 RMVar_ID_44010 Human_SNP_ID_576936557 A-to-I Human chr15 + 50366885 50366885 50366885 CCACCGGACATGTTGGCGTGCACCTCCTGAGTAGCTGGGACTACAGTTGTGCTCTACCACACCGG CCACCGGACATGTTGGCGTGCACCTCCTGAGTCGCTGGGACTACAGTTGTGCTCTACCACACCGG A C GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1247972755 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6433274 44011 RMVar_ID_44011 Human_SNP_ID_576936560 A-to-I Human chr15 + 50366895 50366895 50366895 TGTTGGCGTGCACCTCCTGAGTAGCTGGGACTACAGTTGTGCTCTACCACACCGGGCTAATTTTT TGTTGGCGTGCACCTCCTGAGTAGCTGGGACTGCAGTTGTGCTCTACCACACCGGGCTAATTTTT A G GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs773619656 Functional Loss SNV dbSNP153 33..33 33 - - - 44012 RMVar_ID_44012 Human_SNP_ID_576936568 A-to-I Human chr15 + 50366921 50366921 50366921 GGGACTACAGTTGTGCTCTACCACACCGGGCTAATTTTTGTATTTTTTAGTAGAGACAGGGTTTT GGGACTACAGTTGTGCTCTACCACACCGGGCTGATTTTTGTATTTTTTAGTAGAGACAGGGTTTT A G GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1135747 Functional Loss SNV dbSNP153 33..33 33 - - - 44013 RMVar_ID_44013 Human_SNP_ID_576936576 A-to-I Human chr15 + 50366940 50366940 50366940 ACCACACCGGGCTAATTTTTGTATTTTTTAGTAGAGACAGGGTTTTGCCATGTTAGACAGGCTGG ACCACACCGGGCTAATTTTTGTATTTTTTAGTGGAGACAGGGTTTTGCCATGTTAGACAGGCTGG A G GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1135749 Functional Loss SNV dbSNP153 33..33 33 - - - 44014 RMVar_ID_44014 Human_SNP_ID_576936977 A-to-I Human chr15 + 50368094 50368094 50368094 TAGGTGGGAGGATTGCTTGAGTCCGGGAGTTCAGAACCAGCCTGGACAACATAGTGAGACCCCGT TAGGTGGGAGGATTGCTTGAGTCCGGGAGTTCGGAACCAGCCTGGACAACATAGTGAGACCCCGT A G GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1134908 Functional Loss SNV dbSNP153 33..33 33 - - - 44015 RMVar_ID_44015 Human_SNP_ID_576936978 A-to-I Human chr15 + 50368096 50368096 50368096 GGTGGGAGGATTGCTTGAGTCCGGGAGTTCAGAACCAGCCTGGACAACATAGTGAGACCCCGTCT GGTGGGAGGATTGCTTGAGTCCGGGAGTTCAGTACCAGCCTGGACAACATAGTGAGACCCCGTCT A T GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1201121684 Functional Loss SNV dbSNP153 33..33 33 - - - 44016 RMVar_ID_44016 Human_SNP_ID_576937019 A-to-I Human chr15 + 50368217 50368217 50368217 CCCAGCTACTCAGGAGGCTTGCCTGAGCCCAGAAGTTTGAGACTGCAGTGAGCCATGATATTGCC CCCAGCTACTCAGGAGGCTTGCCTGAGCCCAGCAGTTTGAGACTGCAGTGAGCCATGATATTGCC A C GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1385590772 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17563196 44017 RMVar_ID_44017 Human_SNP_ID_576937025 A-to-I Human chr15 + 50368239 50368239 50368239 CTGAGCCCAGAAGTTTGAGACTGCAGTGAGCCATGATATTGCCAGCCTGGGTGACAGAGCAAGAC CTGAGCCCAGAAGTTTGAGACTGCAGTGAGCCGTGATATTGCCAGCCTGGGTGACAGAGCAAGAC A G GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1026574001 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5258908,Human_RBP_ID_17563196 44018 RMVar_ID_44018 Human_SNP_ID_576937070 A-to-I Human chr15 + 50368414 50368414 50368414 CAGCCTGGCCAACGTGGCAAAACCCCGTCTCTACTAAAAATGCAAAAATTACCGGGACGTGTTGG CAGCCTGGCCAACGTGGCAAAACCCCGTCTCTGCTAAAAATGCAAAAATTACCGGGACGTGTTGG A G GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1431816566 Functional Loss SNV dbSNP153 33..33 33 - - - 44019 RMVar_ID_44019 Human_SNP_ID_576937073 A-to-I Human chr15 + 50368432 50368432 50368432 AAAACCCCGTCTCTACTAAAAATGCAAAAATTACCGGGACGTGTTGGTGAGCACCTGTAATCCCT AAAACCCCGTCTCTACTAAAAATGCAAAAATTGCCGGGACGTGTTGGTGAGCACCTGTAATCCCT A G GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1332392572 Functional Loss SNV dbSNP153 33..33 33 - - - 44020 RMVar_ID_44020 Human_SNP_ID_576937104 A-to-I Human chr15 + 50368534 50368534 50368534 CCAGGGGGTGGAGGTTGCACTGAGCCGAGATCATGCCATTGTACTTCACCTGGGCAACAAGAGGG CCAGGGGGTGGAGGTTGCACTGAGCCGAGATCGTGCCATTGTACTTCACCTGGGCAACAAGAGGG A G GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs372795454 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5095902,Human_RBP_ID_17870114 44021 RMVar_ID_44021 Human_SNP_ID_576937131 A-to-I Human chr15 + 50368629 50368629 50368629 GGCTGGGCACGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGTGGATCACAA GGCTGGGCACGGTGGCTCACACCTGTAATCCCGGCACTTTGGGAGGCCAAGGCGGTGGATCACAA A G GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 29129909,30559470 RNA-Seq:(High) rs887925360 Functional Loss SNV dbSNP153 33..33 33 - - - 44022 RMVar_ID_44022 Human_SNP_ID_576937166 A-to-I Human chr15 + 50368782 50368782 50368782 CCTGTAGTCCCAGCTACTGGGGAGGCTGAGGCAGGAGAATTGCTTTGAACCCGGGAGGCAGAGGT CCTGTAGTCCCAGCTACTGGGGAGGCTGAGGCGGGAGAATTGCTTTGAACCCGGGAGGCAGAGGT A G GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE38233;GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1188321940 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5095903,Human_RBP_ID_25143653 Human_miRNA_ID_3175317 44023 RMVar_ID_44023 Human_SNP_ID_576937387 A-to-I Human chr15 + 50369578 50369578 50369578 CCAGGCAGACAGATCACCAGATGTCGGGAGTTAGAAACCAGCCTGGCCAACATGGCAAAACCCCG CCAGGCAGACAGATCACCAGATGTCGGGAGTTGGAAACCAGCCTGGCCAACATGGCAAAACCCCG A G GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs867580520 Functional Loss SNV dbSNP153 33..33 33 - - - 44024 RMVar_ID_44024 Human_SNP_ID_576937418 A-to-I Human chr15 + 50369686 50369684 50369687 GCCTGTAATCCTAGCTGCTTGGGTGCTGAGTTAGGAGAATTGCTTGAATCCGGGAGGTGGAGGTT GCCTGTAATCCTAGCTGCTTGGGTGCTGAGT___GAGAATTGCTTGAATCCGGGAGGTGGAGGTT TTAG T GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277874247 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_5247055 44025 RMVar_ID_44025 Human_SNP_ID_576937420 A-to-I Human chr15 + 50369686 50369686 50369686 GCCTGTAATCCTAGCTGCTTGGGTGCTGAGTTAGGAGAATTGCTTGAATCCGGGAGGTGGAGGTT GCCTGTAATCCTAGCTGCTTGGGTGCTGAGTTTGGAGAATTGCTTGAATCCGGGAGGTGGAGGTT A T GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1011215285 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5247055 44026 RMVar_ID_44026 Human_SNP_ID_576937453 A-to-I Human chr15 + 50369767 50369767 50369767 GTGTCACTGCACTCCAGCCGGGGCAACAGAGCAAGACTCTGCCTCAAAAAAAAGAAAAAAGAAAT GTGTCACTGCACTCCAGCCGGGGCAACAGAGCGAGACTCTGCCTCAAAAAAAAGAAAAAAGAAAT A G GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1303104712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5247055 44027 RMVar_ID_44027 Human_SNP_ID_576937514 A-to-I Human chr15 + 50369966 50369966 50369966 AAGATTAGCTGGACGTGATGGTGTGTGCCTGTAATCCCAGCTACTCAAGAGGCTGAGGCACAAGA AAGATTAGCTGGACGTGATGGTGTGTGCCTGTGATCCCAGCTACTCAAGAGGCTGAGGCACAAGA A G GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE38233;GSE100210;GSE100210;GSE107867;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,29129909,30559470,31158229 RNA-Seq:(High) rs964073249 Functional Loss SNV dbSNP153 33..33 33 - - - 44028 RMVar_ID_44028 Human_SNP_ID_576937515 A-to-I Human chr15 + 50369966 50369966 50369966 AAGATTAGCTGGACGTGATGGTGTGTGCCTGTAATCCCAGCTACTCAAGAGGCTGAGGCACAAGA AAGATTAGCTGGACGTGATGGTGTGTGCCTGTTATCCCAGCTACTCAAGAGGCTGAGGCACAAGA A T GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE38233;GSE100210;GSE100210;GSE107867;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,29129909,30559470,31158229 RNA-Seq:(High) rs964073249 Functional Loss SNV dbSNP153 33..33 33 - - - 44029 RMVar_ID_44029 Human_SNP_ID_576937518 A-to-I Human chr15 + 50369980 50369980 50369980 GTGATGGTGTGTGCCTGTAATCCCAGCTACTCAAGAGGCTGAGGCACAAGAGAATTGCTTGAACA GTGATGGTGTGTGCCTGTAATCCCAGCTACTCGAGAGGCTGAGGCACAAGAGAATTGCTTGAACA A G GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1163654738 Functional Loss SNV dbSNP153 33..33 33 - - - 44030 RMVar_ID_44030 Human_SNP_ID_576937524 A-to-I Human chr15 + 50370014 50370014 50370014 GAGGCTGAGGCACAAGAGAATTGCTTGAACACAGGAGGTGGAGGTTGCAGTGAGCCAAGATCACG GAGGCTGAGGCACAAGAGAATTGCTTGAACACGGGAGGTGGAGGTTGCAGTGAGCCAAGATCACG A G GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1413487532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8251824 44031 RMVar_ID_44031 Human_SNP_ID_576937602 A-to-I Human chr15 + 50370328 50370328 50370328 ATGTTATGATTAAATTTTATTTTTGTCTGGATACAGTGGCTCACACCTGTAATCCCAGTGCTTTG ATGTTATGATTAAATTTTATTTTTGTCTGGATGCAGTGGCTCACACCTGTAATCCCAGTGCTTTG A G GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs906561039 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_884235,Human_RBP_ID_9345415,Human_RBP_ID_18981471,Human_RBP_ID_19067224,Human_RBP_ID_22540557,Human_RBP_ID_22649888,Human_RBP_ID_25184076 44032 RMVar_ID_44032 Human_SNP_ID_576954767 A-to-I Human chr15 + 50434639 50434638 50434640 GTTTTGCTTTGTTTTGTTTTGTTTTAAAAGACAGGGTCTTGCTGTGTCGCCCAGGTTGAAGTTGT GTTTTGCTTTGTTTTGTTTTGTTTTAAAAGAC__GGTCTTGCTGTGTCGCCCAGGTTGAAGTTGT CAG C USP8 Ensembl:ENSG00000138592 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs905357777 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_12523850 RMVar_hsa_circ_171894,RMVar_hsa_circ_95171,RMVar_hsa_circ_339572,RMVar_hsa_circ_352330,RMVar_hsa_circ_305683,RMVar_hsa_circ_171895,RMVar_hsa_circ_171893 44033 RMVar_ID_44033 Human_SNP_ID_576961989 A-to-I Human chr15 + 50461342 50461342 50461342 AAAATTAGCCAGTCATGATAGTGCACACCTGTAGTCCCAGCTACTCAGGAGGCCAAGGTGGGAGG AAAATTAGCCAGTCATGATAGTGCACACCTGTGGTCCCAGCTACTCAGGAGGCCAAGGTGGGAGG A G USP8 Ensembl:ENSG00000138592 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1406722204 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69367,RMVar_hsa_circ_95171,RMVar_hsa_circ_171895,RMVar_hsa_circ_65196,RMVar_hsa_circ_27260,RMVar_hsa_circ_353189,RMVar_hsa_circ_364869,RMVar_hsa_circ_373161,RMVar_hsa_circ_171900,RMVar_hsa_circ_171901,RMVar_hsa_circ_59162,RMVar_hsa_circ_171903,RMVar_hsa_circ_298122,RMVar_hsa_circ_331463,RMVar_hsa_circ_339564,RMVar_hsa_circ_291992,RMVar_hsa_circ_171905,RMVar_hsa_circ_54779,RMVar_hsa_circ_171904,RMVar_hsa_circ_327613,RMVar_hsa_circ_348146,RMVar_hsa_circ_328135,RMVar_hsa_circ_72671,RMVar_hsa_circ_292103,RMVar_hsa_circ_68957,RMVar_hsa_circ_171906,RMVar_hsa_circ_51693 44034 RMVar_ID_44034 Human_SNP_ID_576965328 A-to-I Human chr15 + 50474970 50474970 50474970 ATCTCTACTAAAATTACAAAAATTTGCCGGGCATGATGGCGGGCGCCTGTGATCCCAGGTACTGA ATCTCTACTAAAATTACAAAAATTTGCCGGGCGTGATGGCGGGCGCCTGTGATCCCAGGTACTGA A G USP8 Ensembl:ENSG00000138592 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965474286 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69367,RMVar_hsa_circ_373161,RMVar_hsa_circ_171901,RMVar_hsa_circ_59162,RMVar_hsa_circ_339564,RMVar_hsa_circ_171905,RMVar_hsa_circ_54779,RMVar_hsa_circ_348146,RMVar_hsa_circ_72671,RMVar_hsa_circ_68957,RMVar_hsa_circ_80824,RMVar_hsa_circ_283206,RMVar_hsa_circ_51693,RMVar_hsa_circ_326281,RMVar_hsa_circ_334920,RMVar_hsa_circ_275912,RMVar_hsa_circ_16796,RMVar_hsa_circ_73048,RMVar_hsa_circ_171910,RMVar_hsa_circ_171911 44035 RMVar_ID_44035 Human_SNP_ID_576965497 A-to-I Human chr15 + 50475633 50475633 50475633 ATTTACTTATTTATTTTTCGAGATGAAGTCTCACTCTTATCCCCCAGGCTGGAGTGCAGTGGCGC ATTTACTTATTTATTTTTCGAGATGAAGTCTCCCTCTTATCCCCCAGGCTGGAGTGCAGTGGCGC A C USP8 Ensembl:ENSG00000138592 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs551793653 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69367,RMVar_hsa_circ_373161,RMVar_hsa_circ_171901,RMVar_hsa_circ_59162,RMVar_hsa_circ_339564,RMVar_hsa_circ_171905,RMVar_hsa_circ_54779,RMVar_hsa_circ_348146,RMVar_hsa_circ_72671,RMVar_hsa_circ_68957,RMVar_hsa_circ_80824,RMVar_hsa_circ_283206,RMVar_hsa_circ_51693,RMVar_hsa_circ_326281,RMVar_hsa_circ_334920,RMVar_hsa_circ_275912,RMVar_hsa_circ_16796,RMVar_hsa_circ_73048,RMVar_hsa_circ_171910,RMVar_hsa_circ_171911 44036 RMVar_ID_44036 Human_SNP_ID_576986490 A-to-I Human chr15 - 50554976 50554976 50554976 CAGGCGCAGTGGCTCGTGCCTGTAATCCCAGCACTTTGGGAGGCAGAGGTGGGTGGATCTGAGAC CAGGCGCAGTGGCTCGTGCCTGTAATCCCAGCTCTTTGGGAGGCAGAGGTGGGTGGATCTGAGAC T A TRPM7 Ensembl:ENSG00000092439 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs370653975 Functional Loss SNV dbSNP153 33..33 33 - - - 44037 RMVar_ID_44037 Human_SNP_ID_576986492 A-to-I Human chr15 - 50554985 50554985 50554985 ATAAGAGGCCAGGCGCAGTGGCTCGTGCCTGTAATCCCAGCACTTTGGGAGGCAGAGGTGGGTGG ATAAGAGGCCAGGCGCAGTGGCTCGTGCCTGTGATCCCAGCACTTTGGGAGGCAGAGGTGGGTGG T C TRPM7 Ensembl:ENSG00000092439 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1286229831 Functional Loss SNV dbSNP153 33..33 33 - - - 44038 RMVar_ID_44038 Human_SNP_ID_576987247 A-to-I Human chr15 - 50557675 50557675 50557675 TGCTGCCACTGCACTCCAGCCTGGGTGACAGCAGAACTCTGTCTCAAAAAAAAGATGTGGAATTC TGCTGCCACTGCACTCCAGCCTGGGTGACAGCCGAACTCTGTCTCAAAAAAAAGATGTGGAATTC T G TRPM7 Ensembl:ENSG00000092439 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1357569362 Functional Loss SNV dbSNP153 33..33 33 - - - 44039 RMVar_ID_44039 Human_SNP_ID_576987254 A-to-I Human chr15 - 50557695 50557695 50557695 AGGTTGCAGTGAGCCTAGATTGCTGCCACTGCACTCCAGCCTGGGTGACAGCAGAACTCTGTCTC AGGTTGCAGTGAGCCTAGATTGCTGCCACTGCGCTCCAGCCTGGGTGACAGCAGAACTCTGTCTC T C TRPM7 Ensembl:ENSG00000092439 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1379996482 Functional Loss SNV dbSNP153 33..33 33 - - - 44040 RMVar_ID_44040 Human_SNP_ID_576987258 A-to-I Human chr15 - 50557709 50557709 50557709 AACCCAAGAGGTGGAGGTTGCAGTGAGCCTAGATTGCTGCCACTGCACTCCAGCCTGGGTGACAG AACCCAAGAGGTGGAGGTTGCAGTGAGCCTAGGTTGCTGCCACTGCACTCCAGCCTGGGTGACAG T C TRPM7 Ensembl:ENSG00000092439 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1403880742 Functional Loss SNV dbSNP153 33..33 33 - - - 44041 RMVar_ID_44041 Human_SNP_ID_576987266 A-to-I Human chr15 - 50557772 50557772 50557772 GGGTGTGGTGGCGCGTGCCTGTAGGCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAA GGGTGTGGTGGCGCGTGCCTGTAGGCCCAGCTCCTCAGGAGGCTGAGGCAGGAGAATTGCTTGAA T G TRPM7 Ensembl:ENSG00000092439 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1473474615 Functional Loss SNV dbSNP153 33..33 33 - - - 44042 RMVar_ID_44042 Human_SNP_ID_576987277 A-to-I Human chr15 - 50557820 50557820 50557820 GGCCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTATCTGGGTGTGGTGGCGCGTG GGCCAACATGGTGAAACCCCGTCTCTACTAAATATACAAAAATTATCTGGGTGTGGTGGCGCGTG T A TRPM7 Ensembl:ENSG00000092439 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs925406251 Functional Loss SNV dbSNP153 33..33 33 - - - 44043 RMVar_ID_44043 Human_SNP_ID_576987278 A-to-I Human chr15 - 50557820 50557820 50557820 GGCCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTATCTGGGTGTGGTGGCGCGTG GGCCAACATGGTGAAACCCCGTCTCTACTAAACATACAAAAATTATCTGGGTGTGGTGGCGCGTG T G TRPM7 Ensembl:ENSG00000092439 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs925406251 Functional Loss SNV dbSNP153 33..33 33 - - - 44044 RMVar_ID_44044 Human_SNP_ID_576987279 A-to-I Human chr15 - 50557826 50557826 50557826 CAGCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTATCTGGGTGTGGTGG CAGCCTGGCCAACATGGTGAAACCCCGTCTCTGCTAAAAATACAAAAATTATCTGGGTGTGGTGG T C TRPM7 Ensembl:ENSG00000092439 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs936683505 Functional Loss SNV dbSNP153 33..33 33 - - - 44045 RMVar_ID_44045 Human_SNP_ID_576987297 A-to-I Human chr15 - 50557894 50557894 50557894 CACGCCTGTAATTCCATCACTTTGGGAGGCCAAGGTGGGTGGATCATCTGAGGTCAGGAGTTCAA CACGCCTGTAATTCCATCACTTTGGGAGGCCAGGGTGGGTGGATCATCTGAGGTCAGGAGTTCAA T C TRPM7 Ensembl:ENSG00000092439 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202581775 Functional Loss SNV dbSNP153 33..33 33 - - - 44046 RMVar_ID_44046 Human_SNP_ID_576987393 A-to-I Human chr15 - 50558326 50558326 50558326 TTGCCCACGCTGGTCTCAAATTCCTGGGCTCAAGTGATCCTCTCGCCTGAGCTTCCCAAAGTGGT TTGCCCACGCTGGTCTCAAATTCCTGGGCTCACGTGATCCTCTCGCCTGAGCTTCCCAAAGTGGT T G TRPM7 Ensembl:ENSG00000092439 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1237741188 Functional Loss SNV dbSNP153 33..33 33 - - - 44047 RMVar_ID_44047 Human_SNP_ID_576987427 A-to-I Human chr15 - 50558449 50558449 50558449 ACCTCAAGTGATCCACCTCCCCCGGCTACCCAAAGTACTGGGATTATAGGTGTGAGCCACCATGC ACCTCAAGTGATCCACCTCCCCCGGCTACCCAGAGTACTGGGATTATAGGTGTGAGCCACCATGC T C TRPM7 Ensembl:ENSG00000092439 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs918822689 Functional Loss SNV dbSNP153 33..33 33 - - - 44048 RMVar_ID_44048 Human_SNP_ID_576987637 A-to-I Human chr15 - 50559176 50559176 50559176 ATGGCGGTGAGTGCCTGTAATCCCAGCTACTCAGGAGTCTGAGGCAGGAGAATTGCTTGAACCTG ATGGCGGTGAGTGCCTGTAATCCCAGCTACTCGGGAGTCTGAGGCAGGAGAATTGCTTGAACCTG T C TRPM7 Ensembl:ENSG00000092439 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1328860939 Functional Loss SNV dbSNP153 33..33 33 - - - 44049 RMVar_ID_44049 Human_SNP_ID_576988512 A-to-I Human chr15 - 50562171 50562171 50562171 CCTAATTCAGCCGGGCATGGTGGCTCACACCTATAATCCCAGCACTTTGGGAGGCCGAGGCAGGT CCTAATTCAGCCGGGCATGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGT T C TRPM7 Ensembl:ENSG00000092439 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1235605638 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_171916 44050 RMVar_ID_44050 Human_SNP_ID_576988580 A-to-I Human chr15 - 50562507 50562507 50562507 CCTTGGCCTTTCAAAGTGCTGAGATTACAGGCATGAGCCACTGCACCCTGCCTTCAAGGCACTTT CCTTGGCCTTTCAAAGTGCTGAGATTACAGGCGTGAGCCACTGCACCCTGCCTTCAAGGCACTTT T C TRPM7 Ensembl:ENSG00000092439 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1197030280 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_171916 44051 RMVar_ID_44051 Human_SNP_ID_576988589 A-to-I Human chr15 - 50562552 50562552 50562552 TTGGCCAGGCTGCTCTTGAACTCCTGACCTCAAATGATTCTCTCACCTTGGCCTTTCAAAGTGCT TTGGCCAGGCTGCTCTTGAACTCCTGACCTCAGATGATTCTCTCACCTTGGCCTTTCAAAGTGCT T C TRPM7 Ensembl:ENSG00000092439 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1235947584 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_171916 44052 RMVar_ID_44052 Human_SNP_ID_576988615 A-to-I Human chr15 - 50562650 50562650 50562650 CTCCCACCTCGGCCTTCTGAGTAGCTGGGACTACAGGCGCACATCACCACACCTGGCTAATTTTT CTCCCACCTCGGCCTTCTGAGTAGCTGGGACTGCAGGCGCACATCACCACACCTGGCTAATTTTT T C TRPM7 Ensembl:ENSG00000092439 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs374407000 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_171916 44053 RMVar_ID_44053 Human_SNP_ID_576989690 A-to-I Human chr15 - 50566530 50566530 50566530 CACCACACCCAGCTAATTTTGTTACTTTTAGTAGAGTCAGGGTTTCACCATGTTGGCCAGGATTG CACCACACCCAGCTAATTTTGTTACTTTTAGTGGAGTCAGGGTTTCACCATGTTGGCCAGGATTG T C TRPM7 Ensembl:ENSG00000092439 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903174399 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_171916 44054 RMVar_ID_44054 Human_SNP_ID_576989698 A-to-I Human chr15 - 50566572 50566572 50566572 CCTGCTTCAGCCTCTTGAGTAACTGGCACTACAGGTACGTGCCACCACACCCAGCTAATTTTGTT CCTGCTTCAGCCTCTTGAGTAACTGGCACTACCGGTACGTGCCACCACACCCAGCTAATTTTGTT T G TRPM7 Ensembl:ENSG00000092439 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs948973501 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8250998 RMVar_hsa_circ_171916 44055 RMVar_ID_44055 Human_SNP_ID_576996346 A-to-I Human chr15 - 50590937 50590937 50590937 AAATTGCCACATTAAGGCCAGCCTAGGAAGTTATCTAGGCACTAAACATGTTGATATTACTTCTA AAATTGCCACATTAAGGCCAGCCTAGGAAGTTTTCTAGGCACTAAACATGTTGATATTACTTCTA T A TRPM7 Ensembl:ENSG00000092439 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs996362242 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_171917,RMVar_hsa_circ_289391,RMVar_hsa_circ_373597,RMVar_hsa_circ_29696,RMVar_hsa_circ_61570,RMVar_hsa_circ_48395,RMVar_hsa_circ_118886,RMVar_hsa_circ_50395,RMVar_hsa_circ_171931,RMVar_hsa_circ_25101,RMVar_hsa_circ_23043,RMVar_hsa_circ_171932,RMVar_hsa_circ_108778,RMVar_hsa_circ_377979,RMVar_hsa_circ_171937,RMVar_hsa_circ_299008,RMVar_hsa_circ_116407,RMVar_hsa_circ_171935,RMVar_hsa_circ_171936,RMVar_hsa_circ_61806,RMVar_hsa_circ_284907,RMVar_hsa_circ_378241,RMVar_hsa_circ_62295,RMVar_hsa_circ_41220,RMVar_hsa_circ_39588,RMVar_hsa_circ_74437,RMVar_hsa_circ_171938,RMVar_hsa_circ_370017,RMVar_hsa_circ_44030,RMVar_hsa_circ_171939 44056 RMVar_ID_44056 Human_SNP_ID_576996386 A-to-I Human chr15 - 50591096 50591096 50591096 GAACATTTCAAAAAGGAATGACTTATTCTTATACCTATGATAGCTTAAATAAGATAAGAACAAAA GAACATTTCAAAAAGGAATGACTTATTCTTATGCCTATGATAGCTTAAATAAGATAAGAACAAAA T C TRPM7 Ensembl:ENSG00000092439 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1566967082 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_171917,RMVar_hsa_circ_289391,RMVar_hsa_circ_373597,RMVar_hsa_circ_29696,RMVar_hsa_circ_61570,RMVar_hsa_circ_48395,RMVar_hsa_circ_118886,RMVar_hsa_circ_50395,RMVar_hsa_circ_171931,RMVar_hsa_circ_25101,RMVar_hsa_circ_23043,RMVar_hsa_circ_171932,RMVar_hsa_circ_108778,RMVar_hsa_circ_377979,RMVar_hsa_circ_171937,RMVar_hsa_circ_299008,RMVar_hsa_circ_116407,RMVar_hsa_circ_171935,RMVar_hsa_circ_171936,RMVar_hsa_circ_61806,RMVar_hsa_circ_284907,RMVar_hsa_circ_378241,RMVar_hsa_circ_62295,RMVar_hsa_circ_41220,RMVar_hsa_circ_39588,RMVar_hsa_circ_74437,RMVar_hsa_circ_171938,RMVar_hsa_circ_370017,RMVar_hsa_circ_44030,RMVar_hsa_circ_171939 44057 RMVar_ID_44057 Human_SNP_ID_576999392 A-to-I Human chr15 - 50602378 50602378 50602378 GCTATCCCTCCCCCTGCCCCCTACCCCATGACAGGCCCCGGTGTATGATGTTCCCTACCCTGTGT GCTATCCCTCCCCCTGCCCCCTACCCCATGACGGGCCCCGGTGTATGATGTTCCCTACCCTGTGT T C TRPM7 Ensembl:ENSG00000092439 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1258169422 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2407,RMVar_hsa_circ_171917,RMVar_hsa_circ_373597,RMVar_hsa_circ_61570,RMVar_hsa_circ_48395,RMVar_hsa_circ_118886,RMVar_hsa_circ_50395,RMVar_hsa_circ_171931,RMVar_hsa_circ_23043,RMVar_hsa_circ_171932,RMVar_hsa_circ_108778,RMVar_hsa_circ_171937,RMVar_hsa_circ_116407,RMVar_hsa_circ_378241,RMVar_hsa_circ_62295,RMVar_hsa_circ_41220,RMVar_hsa_circ_39588,RMVar_hsa_circ_361362,RMVar_hsa_circ_83020,RMVar_hsa_circ_70540,RMVar_hsa_circ_38798,RMVar_hsa_circ_171943,RMVar_hsa_circ_41632,RMVar_hsa_circ_18003,RMVar_hsa_circ_38795,RMVar_hsa_circ_18813,RMVar_hsa_circ_40786,RMVar_hsa_circ_48646,RMVar_hsa_circ_75311,RMVar_hsa_circ_37030 44058 RMVar_ID_44058 Human_SNP_ID_576999403 A-to-I Human chr15 - 50602407 50602407 50602407 CATCATTTACATTAGGTATTTATCCTAATGCTATCCCTCCCCCTGCCCCCTACCCCATGACAGGC CATCATTTACATTAGGTATTTATCCTAATGCTGTCCCTCCCCCTGCCCCCTACCCCATGACAGGC T C TRPM7 Ensembl:ENSG00000092439 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1015370183 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2407,RMVar_hsa_circ_171917,RMVar_hsa_circ_373597,RMVar_hsa_circ_61570,RMVar_hsa_circ_48395,RMVar_hsa_circ_118886,RMVar_hsa_circ_50395,RMVar_hsa_circ_171931,RMVar_hsa_circ_23043,RMVar_hsa_circ_171932,RMVar_hsa_circ_108778,RMVar_hsa_circ_171937,RMVar_hsa_circ_116407,RMVar_hsa_circ_378241,RMVar_hsa_circ_62295,RMVar_hsa_circ_41220,RMVar_hsa_circ_39588,RMVar_hsa_circ_361362,RMVar_hsa_circ_83020,RMVar_hsa_circ_70540,RMVar_hsa_circ_38798,RMVar_hsa_circ_171943,RMVar_hsa_circ_41632,RMVar_hsa_circ_18003,RMVar_hsa_circ_38795,RMVar_hsa_circ_18813,RMVar_hsa_circ_40786,RMVar_hsa_circ_48646,RMVar_hsa_circ_75311,RMVar_hsa_circ_37030 44059 RMVar_ID_44059 Human_SNP_ID_576999406 A-to-I Human chr15 - 50602413 50602413 50602413 TTAACTCATCATTTACATTAGGTATTTATCCTAATGCTATCCCTCCCCCTGCCCCCTACCCCATG TTAACTCATCATTTACATTAGGTATTTATCCTGATGCTATCCCTCCCCCTGCCCCCTACCCCATG T C TRPM7 Ensembl:ENSG00000092439 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs760939508 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2407,RMVar_hsa_circ_171917,RMVar_hsa_circ_373597,RMVar_hsa_circ_61570,RMVar_hsa_circ_48395,RMVar_hsa_circ_118886,RMVar_hsa_circ_50395,RMVar_hsa_circ_171931,RMVar_hsa_circ_23043,RMVar_hsa_circ_171932,RMVar_hsa_circ_108778,RMVar_hsa_circ_171937,RMVar_hsa_circ_116407,RMVar_hsa_circ_378241,RMVar_hsa_circ_62295,RMVar_hsa_circ_41220,RMVar_hsa_circ_39588,RMVar_hsa_circ_361362,RMVar_hsa_circ_83020,RMVar_hsa_circ_70540,RMVar_hsa_circ_38798,RMVar_hsa_circ_171943,RMVar_hsa_circ_41632,RMVar_hsa_circ_18003,RMVar_hsa_circ_38795,RMVar_hsa_circ_18813,RMVar_hsa_circ_40786,RMVar_hsa_circ_48646,RMVar_hsa_circ_75311,RMVar_hsa_circ_37030 44060 RMVar_ID_44060 Human_SNP_ID_576999419 A-to-I Human chr15 - 50602482 50602482 50602482 TCAAAGGAGTTTAGAAAATACGTAGGATTTACATAGGTATACATGCACCATGTTGGTTTGCTGCA TCAAAGGAGTTTAGAAAATACGTAGGATTTACCTAGGTATACATGCACCATGTTGGTTTGCTGCA T G TRPM7 Ensembl:ENSG00000092439 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1401771475 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2443703 RMVar_hsa_circ_2407,RMVar_hsa_circ_171917,RMVar_hsa_circ_373597,RMVar_hsa_circ_61570,RMVar_hsa_circ_48395,RMVar_hsa_circ_118886,RMVar_hsa_circ_50395,RMVar_hsa_circ_171931,RMVar_hsa_circ_23043,RMVar_hsa_circ_171932,RMVar_hsa_circ_108778,RMVar_hsa_circ_171937,RMVar_hsa_circ_116407,RMVar_hsa_circ_378241,RMVar_hsa_circ_62295,RMVar_hsa_circ_41220,RMVar_hsa_circ_39588,RMVar_hsa_circ_361362,RMVar_hsa_circ_83020,RMVar_hsa_circ_70540,RMVar_hsa_circ_38798,RMVar_hsa_circ_171943,RMVar_hsa_circ_41632,RMVar_hsa_circ_18003,RMVar_hsa_circ_38795,RMVar_hsa_circ_18813,RMVar_hsa_circ_40786,RMVar_hsa_circ_48646,RMVar_hsa_circ_75311,RMVar_hsa_circ_37030 44061 RMVar_ID_44061 Human_SNP_ID_576999752 A-to-I Human chr15 - 50603728 50603728 50603728 AATCTTAGAAAATCAGTCTTCTCTTGGAACCAACCCAAATGTCCATCAATGATAGACTGGATTAA AATCTTAGAAAATCAGTCTTCTCTTGGAACCAGCCCAAATGTCCATCAATGATAGACTGGATTAA T C TRPM7 Ensembl:ENSG00000092439 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs944520716 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3476078 RMVar_hsa_circ_2407,RMVar_hsa_circ_171917,RMVar_hsa_circ_373597,RMVar_hsa_circ_61570,RMVar_hsa_circ_48395,RMVar_hsa_circ_118886,RMVar_hsa_circ_50395,RMVar_hsa_circ_171931,RMVar_hsa_circ_23043,RMVar_hsa_circ_171932,RMVar_hsa_circ_108778,RMVar_hsa_circ_171937,RMVar_hsa_circ_116407,RMVar_hsa_circ_378241,RMVar_hsa_circ_62295,RMVar_hsa_circ_41220,RMVar_hsa_circ_39588,RMVar_hsa_circ_361362,RMVar_hsa_circ_83020,RMVar_hsa_circ_70540,RMVar_hsa_circ_38798,RMVar_hsa_circ_171943,RMVar_hsa_circ_41632,RMVar_hsa_circ_18003,RMVar_hsa_circ_38795,RMVar_hsa_circ_18813,RMVar_hsa_circ_40786,RMVar_hsa_circ_48646,RMVar_hsa_circ_75311,RMVar_hsa_circ_37030 44062 RMVar_ID_44062 Human_SNP_ID_577008992 A-to-I Human chr15 - 50635863 50635863 50635863 GCGATTCTCATCCCTCAGCCTCCCGAGTAGCTAGGATTACAGGCACTCGCCACCACGCCCCAGCT GCGATTCTCATCCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCACTCGCCACCACGCCCCAGCT T C TRPM7 Ensembl:ENSG00000092439 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1293014516 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23043,RMVar_hsa_circ_62295,RMVar_hsa_circ_83020,RMVar_hsa_circ_70540,RMVar_hsa_circ_171943,RMVar_hsa_circ_41632,RMVar_hsa_circ_27742,RMVar_hsa_circ_265078,RMVar_hsa_circ_6285,RMVar_hsa_circ_68559,RMVar_hsa_circ_171946,RMVar_hsa_circ_111354,RMVar_hsa_circ_171951,RMVar_hsa_circ_120421,RMVar_hsa_circ_27680,RMVar_hsa_circ_23862,RMVar_hsa_circ_62672,RMVar_hsa_circ_30216,RMVar_hsa_circ_373085,RMVar_hsa_circ_171952,RMVar_hsa_circ_321083,RMVar_hsa_circ_124115,RMVar_hsa_circ_171953,RMVar_hsa_circ_171954,RMVar_hsa_circ_369345,RMVar_hsa_circ_92321,RMVar_hsa_circ_171956,RMVar_hsa_circ_171957,RMVar_hsa_circ_171955,RMVar_hsa_circ_298753,RMVar_hsa_circ_171959,RMVar_hsa_circ_20406,RMVar_hsa_circ_113002,RMVar_hsa_circ_171958,RMVar_hsa_circ_316359,RMVar_hsa_circ_267628,RMVar_hsa_circ_72351,RMVar_hsa_circ_171964,RMVar_hsa_circ_171963,RMVar_hsa_circ_326377,RMVar_hsa_circ_59603,RMVar_hsa_circ_270074,RMVar_hsa_circ_328708,RMVar_hsa_circ_344300,RMVar_hsa_circ_281506,RMVar_hsa_circ_171966,RMVar_hsa_circ_171967,RMVar_hsa_circ_171965,RMVar_hsa_circ_171972,RMVar_hsa_circ_171970,RMVar_hsa_circ_369466,RMVar_hsa_circ_378529,RMVar_hsa_circ_171971,RMVar_hsa_circ_292354,RMVar_hsa_circ_361508,RMVar_hsa_circ_171973 44063 RMVar_ID_44063 Human_SNP_ID_577009150 A-to-I Human chr15 - 50636302 50636302 50636302 CTTGTAGTCCCAGCTTCTTGGGAGGCTGAGACAGGAGAATTGTTTGAGCCCAGGAGGCGGAGGCT CTTGTAGTCCCAGCTTCTTGGGAGGCTGAGACGGGAGAATTGTTTGAGCCCAGGAGGCGGAGGCT T C TRPM7 Ensembl:ENSG00000092439 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1305415739 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25144356 RMVar_hsa_circ_23043,RMVar_hsa_circ_62295,RMVar_hsa_circ_83020,RMVar_hsa_circ_70540,RMVar_hsa_circ_171943,RMVar_hsa_circ_41632,RMVar_hsa_circ_27742,RMVar_hsa_circ_265078,RMVar_hsa_circ_6285,RMVar_hsa_circ_68559,RMVar_hsa_circ_171946,RMVar_hsa_circ_111354,RMVar_hsa_circ_171951,RMVar_hsa_circ_120421,RMVar_hsa_circ_27680,RMVar_hsa_circ_23862,RMVar_hsa_circ_62672,RMVar_hsa_circ_30216,RMVar_hsa_circ_373085,RMVar_hsa_circ_171952,RMVar_hsa_circ_321083,RMVar_hsa_circ_124115,RMVar_hsa_circ_171953,RMVar_hsa_circ_171954,RMVar_hsa_circ_369345,RMVar_hsa_circ_92321,RMVar_hsa_circ_171956,RMVar_hsa_circ_171957,RMVar_hsa_circ_171955,RMVar_hsa_circ_298753,RMVar_hsa_circ_171959,RMVar_hsa_circ_20406,RMVar_hsa_circ_113002,RMVar_hsa_circ_171958,RMVar_hsa_circ_316359,RMVar_hsa_circ_267628,RMVar_hsa_circ_72351,RMVar_hsa_circ_171964,RMVar_hsa_circ_171963,RMVar_hsa_circ_326377,RMVar_hsa_circ_59603,RMVar_hsa_circ_270074,RMVar_hsa_circ_328708,RMVar_hsa_circ_344300,RMVar_hsa_circ_281506,RMVar_hsa_circ_171966,RMVar_hsa_circ_171967,RMVar_hsa_circ_171965,RMVar_hsa_circ_171972,RMVar_hsa_circ_171970,RMVar_hsa_circ_369466,RMVar_hsa_circ_378529,RMVar_hsa_circ_171971,RMVar_hsa_circ_292354,RMVar_hsa_circ_361508,RMVar_hsa_circ_171973 44064 RMVar_ID_44064 Human_SNP_ID_577009174 A-to-I Human chr15 - 50636364 50636364 50636364 CAGTATGGTGAAACCCTGTCTCTCCTAAAAATACAAAAATTAGCCGAGCGTGGTGGCGTGTGCTT CAGTATGGTGAAACCCTGTCTCTCCTAAAAATGCAAAAATTAGCCGAGCGTGGTGGCGTGTGCTT T C TRPM7 Ensembl:ENSG00000092439 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs940928079 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23043,RMVar_hsa_circ_62295,RMVar_hsa_circ_83020,RMVar_hsa_circ_70540,RMVar_hsa_circ_171943,RMVar_hsa_circ_41632,RMVar_hsa_circ_27742,RMVar_hsa_circ_265078,RMVar_hsa_circ_6285,RMVar_hsa_circ_68559,RMVar_hsa_circ_171946,RMVar_hsa_circ_111354,RMVar_hsa_circ_171951,RMVar_hsa_circ_120421,RMVar_hsa_circ_27680,RMVar_hsa_circ_23862,RMVar_hsa_circ_62672,RMVar_hsa_circ_30216,RMVar_hsa_circ_373085,RMVar_hsa_circ_171952,RMVar_hsa_circ_321083,RMVar_hsa_circ_124115,RMVar_hsa_circ_171953,RMVar_hsa_circ_171954,RMVar_hsa_circ_369345,RMVar_hsa_circ_92321,RMVar_hsa_circ_171956,RMVar_hsa_circ_171957,RMVar_hsa_circ_171955,RMVar_hsa_circ_298753,RMVar_hsa_circ_171959,RMVar_hsa_circ_20406,RMVar_hsa_circ_113002,RMVar_hsa_circ_171958,RMVar_hsa_circ_316359,RMVar_hsa_circ_267628,RMVar_hsa_circ_72351,RMVar_hsa_circ_171964,RMVar_hsa_circ_171963,RMVar_hsa_circ_326377,RMVar_hsa_circ_59603,RMVar_hsa_circ_270074,RMVar_hsa_circ_328708,RMVar_hsa_circ_344300,RMVar_hsa_circ_281506,RMVar_hsa_circ_171966,RMVar_hsa_circ_171967,RMVar_hsa_circ_171965,RMVar_hsa_circ_171972,RMVar_hsa_circ_171970,RMVar_hsa_circ_369466,RMVar_hsa_circ_378529,RMVar_hsa_circ_171971,RMVar_hsa_circ_292354,RMVar_hsa_circ_361508,RMVar_hsa_circ_171973 44065 RMVar_ID_44065 Human_SNP_ID_577009186 A-to-I Human chr15 - 50636395 50636395 50636395 CCTGAGGTCAGGAATTCTAGACCAGACTGACCAGTATGGTGAAACCCTGTCTCTCCTAAAAATAC CCTGAGGTCAGGAATTCTAGACCAGACTGACCGGTATGGTGAAACCCTGTCTCTCCTAAAAATAC T C TRPM7 Ensembl:ENSG00000092439 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs912895393 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23043,RMVar_hsa_circ_62295,RMVar_hsa_circ_83020,RMVar_hsa_circ_70540,RMVar_hsa_circ_171943,RMVar_hsa_circ_41632,RMVar_hsa_circ_27742,RMVar_hsa_circ_265078,RMVar_hsa_circ_6285,RMVar_hsa_circ_68559,RMVar_hsa_circ_171946,RMVar_hsa_circ_111354,RMVar_hsa_circ_171951,RMVar_hsa_circ_120421,RMVar_hsa_circ_27680,RMVar_hsa_circ_23862,RMVar_hsa_circ_62672,RMVar_hsa_circ_30216,RMVar_hsa_circ_373085,RMVar_hsa_circ_171952,RMVar_hsa_circ_321083,RMVar_hsa_circ_124115,RMVar_hsa_circ_171953,RMVar_hsa_circ_171954,RMVar_hsa_circ_369345,RMVar_hsa_circ_92321,RMVar_hsa_circ_171956,RMVar_hsa_circ_171957,RMVar_hsa_circ_171955,RMVar_hsa_circ_298753,RMVar_hsa_circ_171959,RMVar_hsa_circ_20406,RMVar_hsa_circ_113002,RMVar_hsa_circ_171958,RMVar_hsa_circ_316359,RMVar_hsa_circ_267628,RMVar_hsa_circ_72351,RMVar_hsa_circ_171964,RMVar_hsa_circ_171963,RMVar_hsa_circ_326377,RMVar_hsa_circ_59603,RMVar_hsa_circ_270074,RMVar_hsa_circ_328708,RMVar_hsa_circ_344300,RMVar_hsa_circ_281506,RMVar_hsa_circ_171966,RMVar_hsa_circ_171967,RMVar_hsa_circ_171965,RMVar_hsa_circ_171972,RMVar_hsa_circ_171970,RMVar_hsa_circ_369466,RMVar_hsa_circ_378529,RMVar_hsa_circ_171971,RMVar_hsa_circ_292354,RMVar_hsa_circ_361508,RMVar_hsa_circ_171973 44066 RMVar_ID_44066 Human_SNP_ID_577014906 A-to-I Human chr15 - 50655927 50655927 50655927 GGCATACAGTGGTGCGATCTCAGCTCACAGCAACCTTTGCCTCCCAGGTTCAAGTGATTCTCCTG GGCATACAGTGGTGCGATCTCAGCTCACAGCATCCTTTGCCTCCCAGGTTCAAGTGATTCTCCTG T A TRPM7 Ensembl:ENSG00000092439 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs563856318 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83020,RMVar_hsa_circ_70540,RMVar_hsa_circ_171943,RMVar_hsa_circ_27742,RMVar_hsa_circ_265078,RMVar_hsa_circ_171946,RMVar_hsa_circ_27680,RMVar_hsa_circ_62672,RMVar_hsa_circ_373085,RMVar_hsa_circ_124115,RMVar_hsa_circ_171954,RMVar_hsa_circ_171957,RMVar_hsa_circ_20406,RMVar_hsa_circ_171958,RMVar_hsa_circ_72351,RMVar_hsa_circ_171964,RMVar_hsa_circ_326377,RMVar_hsa_circ_281506,RMVar_hsa_circ_171965,RMVar_hsa_circ_361508,RMVar_hsa_circ_171973,RMVar_hsa_circ_57110,RMVar_hsa_circ_25196,RMVar_hsa_circ_308370,RMVar_hsa_circ_171976,RMVar_hsa_circ_304702,RMVar_hsa_circ_329727,RMVar_hsa_circ_171977,RMVar_hsa_circ_297854,RMVar_hsa_circ_86763,RMVar_hsa_circ_52901,RMVar_hsa_circ_171978,RMVar_hsa_circ_171979,RMVar_hsa_circ_275658,RMVar_hsa_circ_171982,RMVar_hsa_circ_171983 44067 RMVar_ID_44067 Human_SNP_ID_577014907 A-to-I Human chr15 - 50655927 50655927 50655927 GGCATACAGTGGTGCGATCTCAGCTCACAGCAACCTTTGCCTCCCAGGTTCAAGTGATTCTCCTG GGCATACAGTGGTGCGATCTCAGCTCACAGCAGCCTTTGCCTCCCAGGTTCAAGTGATTCTCCTG T C TRPM7 Ensembl:ENSG00000092439 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs563856318 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83020,RMVar_hsa_circ_70540,RMVar_hsa_circ_171943,RMVar_hsa_circ_27742,RMVar_hsa_circ_265078,RMVar_hsa_circ_171946,RMVar_hsa_circ_27680,RMVar_hsa_circ_62672,RMVar_hsa_circ_373085,RMVar_hsa_circ_124115,RMVar_hsa_circ_171954,RMVar_hsa_circ_171957,RMVar_hsa_circ_20406,RMVar_hsa_circ_171958,RMVar_hsa_circ_72351,RMVar_hsa_circ_171964,RMVar_hsa_circ_326377,RMVar_hsa_circ_281506,RMVar_hsa_circ_171965,RMVar_hsa_circ_361508,RMVar_hsa_circ_171973,RMVar_hsa_circ_57110,RMVar_hsa_circ_25196,RMVar_hsa_circ_308370,RMVar_hsa_circ_171976,RMVar_hsa_circ_304702,RMVar_hsa_circ_329727,RMVar_hsa_circ_171977,RMVar_hsa_circ_297854,RMVar_hsa_circ_86763,RMVar_hsa_circ_52901,RMVar_hsa_circ_171978,RMVar_hsa_circ_171979,RMVar_hsa_circ_275658,RMVar_hsa_circ_171982,RMVar_hsa_circ_171983 44068 RMVar_ID_44068 Human_SNP_ID_577015634 A-to-I Human chr15 - 50658454 50658454 50658454 GGAATCCTCCCACCTCAGCCTCCCTAGTAGCTAGGACTATAGGCCTGCACCACTACCCCTAGCTA GGAATCCTCCCACCTCAGCCTCCCTAGTAGCTGGGACTATAGGCCTGCACCACTACCCCTAGCTA T C TRPM7 Ensembl:ENSG00000092439 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1172834593 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83020,RMVar_hsa_circ_70540,RMVar_hsa_circ_171943,RMVar_hsa_circ_27742,RMVar_hsa_circ_265078,RMVar_hsa_circ_171946,RMVar_hsa_circ_27680,RMVar_hsa_circ_62672,RMVar_hsa_circ_373085,RMVar_hsa_circ_171954,RMVar_hsa_circ_20406,RMVar_hsa_circ_171958,RMVar_hsa_circ_171964,RMVar_hsa_circ_326377,RMVar_hsa_circ_281506,RMVar_hsa_circ_171965,RMVar_hsa_circ_361508,RMVar_hsa_circ_171973,RMVar_hsa_circ_308370,RMVar_hsa_circ_171976,RMVar_hsa_circ_304702,RMVar_hsa_circ_171977,RMVar_hsa_circ_297854,RMVar_hsa_circ_86763,RMVar_hsa_circ_171978,RMVar_hsa_circ_171979,RMVar_hsa_circ_275658,RMVar_hsa_circ_171982,RMVar_hsa_circ_171983,RMVar_hsa_circ_306191,RMVar_hsa_circ_171984 44069 RMVar_ID_44069 Human_SNP_ID_577015805 A-to-I Human chr15 - 50658942 50658942 50658942 CTCCCGCCTCAGCCTCCCAAAGTGCTGGCATTACAGGCGTGAGCCACTGCGCCTGGCCACTAGTT CTCCCGCCTCAGCCTCCCAAAGTGCTGGCATTGCAGGCGTGAGCCACTGCGCCTGGCCACTAGTT T C TRPM7 Ensembl:ENSG00000092439 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1211424820 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83020,RMVar_hsa_circ_70540,RMVar_hsa_circ_171943,RMVar_hsa_circ_27742,RMVar_hsa_circ_265078,RMVar_hsa_circ_171946,RMVar_hsa_circ_27680,RMVar_hsa_circ_62672,RMVar_hsa_circ_373085,RMVar_hsa_circ_171954,RMVar_hsa_circ_20406,RMVar_hsa_circ_171958,RMVar_hsa_circ_171964,RMVar_hsa_circ_326377,RMVar_hsa_circ_281506,RMVar_hsa_circ_171965,RMVar_hsa_circ_361508,RMVar_hsa_circ_171973,RMVar_hsa_circ_308370,RMVar_hsa_circ_171976,RMVar_hsa_circ_304702,RMVar_hsa_circ_171977,RMVar_hsa_circ_297854,RMVar_hsa_circ_86763,RMVar_hsa_circ_171978,RMVar_hsa_circ_171979,RMVar_hsa_circ_275658,RMVar_hsa_circ_171982,RMVar_hsa_circ_171983,RMVar_hsa_circ_306191,RMVar_hsa_circ_171984 44070 RMVar_ID_44070 Human_SNP_ID_577015824 A-to-I Human chr15 - 50659009 50659009 50659009 TATTTTTAGTAGAGACGGGGTTTCACTGCGTTAGCCAGGATGGTCTTGATCTCCTGACCTCGTGA TATTTTTAGTAGAGACGGGGTTTCACTGCGTTGGCCAGGATGGTCTTGATCTCCTGACCTCGTGA T C TRPM7 Ensembl:ENSG00000092439 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1048551163 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83020,RMVar_hsa_circ_70540,RMVar_hsa_circ_171943,RMVar_hsa_circ_27742,RMVar_hsa_circ_265078,RMVar_hsa_circ_171946,RMVar_hsa_circ_27680,RMVar_hsa_circ_62672,RMVar_hsa_circ_373085,RMVar_hsa_circ_171954,RMVar_hsa_circ_20406,RMVar_hsa_circ_171958,RMVar_hsa_circ_171964,RMVar_hsa_circ_326377,RMVar_hsa_circ_281506,RMVar_hsa_circ_171965,RMVar_hsa_circ_361508,RMVar_hsa_circ_171973,RMVar_hsa_circ_308370,RMVar_hsa_circ_171976,RMVar_hsa_circ_304702,RMVar_hsa_circ_171977,RMVar_hsa_circ_297854,RMVar_hsa_circ_86763,RMVar_hsa_circ_171978,RMVar_hsa_circ_171979,RMVar_hsa_circ_275658,RMVar_hsa_circ_171982,RMVar_hsa_circ_171983,RMVar_hsa_circ_306191,RMVar_hsa_circ_171984 44071 RMVar_ID_44071 Human_SNP_ID_577016028 A-to-I Human chr15 - 50659806 50659806 50659806 AAAACTAGCTGGGCGTGGTGGTGGGCACTTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGA AAAACTAGCTGGGCGTGGTGGTGGGCACTTGTCATCCCAGCTACTTGGGAGGCTGAGGCAGGAGA T G TRPM7 Ensembl:ENSG00000092439 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1205046100 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83020,RMVar_hsa_circ_70540,RMVar_hsa_circ_171943,RMVar_hsa_circ_27742,RMVar_hsa_circ_265078,RMVar_hsa_circ_171946,RMVar_hsa_circ_27680,RMVar_hsa_circ_62672,RMVar_hsa_circ_373085,RMVar_hsa_circ_171954,RMVar_hsa_circ_20406,RMVar_hsa_circ_171958,RMVar_hsa_circ_171964,RMVar_hsa_circ_326377,RMVar_hsa_circ_281506,RMVar_hsa_circ_171965,RMVar_hsa_circ_361508,RMVar_hsa_circ_171973,RMVar_hsa_circ_308370,RMVar_hsa_circ_171976,RMVar_hsa_circ_304702,RMVar_hsa_circ_171977,RMVar_hsa_circ_297854,RMVar_hsa_circ_86763,RMVar_hsa_circ_171978,RMVar_hsa_circ_171979,RMVar_hsa_circ_275658,RMVar_hsa_circ_171982,RMVar_hsa_circ_171983,RMVar_hsa_circ_306191,RMVar_hsa_circ_171984 44072 RMVar_ID_44072 Human_SNP_ID_577016351 A-to-I Human chr15 - 50661093 50661093 50661093 GGGCACCTGTCATCCCAGCTACTTGGGAGGCTAAGGCAGGAGAATTGCTTGACACTGGAAGGCAG GGGCACCTGTCATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATTGCTTGACACTGGAAGGCAG T C TRPM7 Ensembl:ENSG00000092439 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs574845720 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83020,RMVar_hsa_circ_70540,RMVar_hsa_circ_171943,RMVar_hsa_circ_27742,RMVar_hsa_circ_265078,RMVar_hsa_circ_171946,RMVar_hsa_circ_27680,RMVar_hsa_circ_62672,RMVar_hsa_circ_373085,RMVar_hsa_circ_171954,RMVar_hsa_circ_20406,RMVar_hsa_circ_171958,RMVar_hsa_circ_171964,RMVar_hsa_circ_326377,RMVar_hsa_circ_281506,RMVar_hsa_circ_171965,RMVar_hsa_circ_361508,RMVar_hsa_circ_171973,RMVar_hsa_circ_308370,RMVar_hsa_circ_171976,RMVar_hsa_circ_304702,RMVar_hsa_circ_171977,RMVar_hsa_circ_297854,RMVar_hsa_circ_86763,RMVar_hsa_circ_171978,RMVar_hsa_circ_171979,RMVar_hsa_circ_275658,RMVar_hsa_circ_171982,RMVar_hsa_circ_171983,RMVar_hsa_circ_306191,RMVar_hsa_circ_171984 44073 RMVar_ID_44073 Human_SNP_ID_577016357 A-to-I Human chr15 - 50661128 50661128 50661128 TACTAAAAATACAAAAATTAGCCAGACGTGGTAGTGGGCACCTGTCATCCCAGCTACTTGGGAGG TACTAAAAATACAAAAATTAGCCAGACGTGGTGGTGGGCACCTGTCATCCCAGCTACTTGGGAGG T C TRPM7 Ensembl:ENSG00000092439 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs545438149 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83020,RMVar_hsa_circ_70540,RMVar_hsa_circ_171943,RMVar_hsa_circ_27742,RMVar_hsa_circ_265078,RMVar_hsa_circ_171946,RMVar_hsa_circ_27680,RMVar_hsa_circ_62672,RMVar_hsa_circ_373085,RMVar_hsa_circ_171954,RMVar_hsa_circ_20406,RMVar_hsa_circ_171958,RMVar_hsa_circ_171964,RMVar_hsa_circ_326377,RMVar_hsa_circ_281506,RMVar_hsa_circ_171965,RMVar_hsa_circ_361508,RMVar_hsa_circ_171973,RMVar_hsa_circ_308370,RMVar_hsa_circ_171976,RMVar_hsa_circ_304702,RMVar_hsa_circ_171977,RMVar_hsa_circ_297854,RMVar_hsa_circ_86763,RMVar_hsa_circ_171978,RMVar_hsa_circ_171979,RMVar_hsa_circ_275658,RMVar_hsa_circ_171982,RMVar_hsa_circ_171983,RMVar_hsa_circ_306191,RMVar_hsa_circ_171984 44074 RMVar_ID_44074 Human_SNP_ID_577019221 A-to-I Human chr15 - 50671715 50671715 50671715 ACCTCAAACTCCTGGGCTCAAATGATCCTCCCACCTTAGCTTCCCAGGTAGCTGGGACTATAGGC ACCTCAAACTCCTGGGCTCAAATGATCCTCCCGCCTTAGCTTCCCAGGTAGCTGGGACTATAGGC T C TRPM7 Ensembl:ENSG00000092439 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs890564728 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83020,RMVar_hsa_circ_171943,RMVar_hsa_circ_265078,RMVar_hsa_circ_86763,RMVar_hsa_circ_171978,RMVar_hsa_circ_171983 44075 RMVar_ID_44075 Human_SNP_ID_577019226 A-to-I Human chr15 - 50671726 50671726 50671726 AGCTTACTTTAACCTCAAACTCCTGGGCTCAAATGATCCTCCCACCTTAGCTTCCCAGGTAGCTG AGCTTACTTTAACCTCAAACTCCTGGGCTCAAGTGATCCTCCCACCTTAGCTTCCCAGGTAGCTG T C TRPM7 Ensembl:ENSG00000092439 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1409067552 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12525957 RMVar_hsa_circ_83020,RMVar_hsa_circ_171943,RMVar_hsa_circ_265078,RMVar_hsa_circ_86763,RMVar_hsa_circ_171978,RMVar_hsa_circ_171983 44076 RMVar_ID_44076 Human_SNP_ID_577022147 A-to-I Human chr15 - 50680538 50680538 50680538 TGAGACAAGTGTCTCTCTCTGTCAATTAGGCTAGAGTTCAGTGGTGCGATCTTGGCTCATTGCAG TGAGACAAGTGTCTCTCTCTGTCAATTAGGCTGGAGTTCAGTGGTGCGATCTTGGCTCATTGCAG T C TRPM7 Ensembl:ENSG00000092439 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1351938686 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6434088,Human_RBP_ID_12526160,Human_RBP_ID_18663912 RMVar_hsa_circ_83020,RMVar_hsa_circ_171943,RMVar_hsa_circ_265078,RMVar_hsa_circ_86763,RMVar_hsa_circ_171978 44077 RMVar_ID_44077 Human_SNP_ID_577023286 A-to-I Human chr15 - 50684269 50684269 50684269 CGGGCGTGGTAATCCTAGCTACTCAGGAGGCTAAGGCAGGAGAATCGCTTGAACCTGGGAGGTGG CGGGCGTGGTAATCCTAGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACCTGGGAGGTGG T C TRPM7 Ensembl:ENSG00000092439 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1299295207 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83020,RMVar_hsa_circ_171943,RMVar_hsa_circ_265078,RMVar_hsa_circ_86763,RMVar_hsa_circ_171978 44078 RMVar_ID_44078 Human_SNP_ID_577023288 A-to-I Human chr15 - 50684277 50684277 50684277 TCAGTAATCGGGCGTGGTAATCCTAGCTACTCAGGAGGCTAAGGCAGGAGAATCGCTTGAACCTG TCAGTAATCGGGCGTGGTAATCCTAGCTACTCGGGAGGCTAAGGCAGGAGAATCGCTTGAACCTG T C TRPM7 Ensembl:ENSG00000092439 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs979817273 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83020,RMVar_hsa_circ_171943,RMVar_hsa_circ_265078,RMVar_hsa_circ_86763,RMVar_hsa_circ_171978 44079 RMVar_ID_44079 Human_SNP_ID_577023590 A-to-I Human chr15 - 50685298 50685298 50685298 CACCATGCCCGGCTAATTTTTGCATTTTTAGTAGAGACGGGGTTTCACCATGTTTGGCAGGCTCG CACCATGCCCGGCTAATTTTTGCATTTTTAGTGGAGACGGGGTTTCACCATGTTTGGCAGGCTCG T C TRPM7 Ensembl:ENSG00000092439 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1248643138 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12526271 RMVar_hsa_circ_83020,RMVar_hsa_circ_171943,RMVar_hsa_circ_265078,RMVar_hsa_circ_86763,RMVar_hsa_circ_171978 44080 RMVar_ID_44080 Human_SNP_ID_577028454 A-to-I Human chr15 - 50703097 50703097 50703097 TGTGTCTGTGAATAGTGACTGCACTCCAGCCTAGGTGACATAGCAAGATGCCATCTCAAAGAAAT TGTGTCTGTGAATAGTGACTGCACTCCAGCCTGGGTGACATAGCAAGATGCCATCTCAAAGAAAT T C SPPL2A Ensembl:ENSG00000138600 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1132239 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8183064,Human_RBP_ID_12526304,Human_RBP_ID_21887744,Human_RBP_ID_23654810,Human_RBP_ID_26434396 44081 RMVar_ID_44081 Human_SNP_ID_577028461 A-to-I Human chr15 - 50703158 50703158 50703158 TACTGGCTGAGATGGGAGGGTCCCTTGAGCCCAGGAGTTTGAGGCTGTAGTGAGCTGTGATTGTG TACTGGCTGAGATGGGAGGGTCCCTTGAGCCCGGGAGTTTGAGGCTGTAGTGAGCTGTGATTGTG T C SPPL2A Ensembl:ENSG00000138600 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1132238 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26438591 44082 RMVar_ID_44082 Human_SNP_ID_577028719 A-to-I Human chr15 - 50703628 50703628 50703628 GGCCGGGTGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGTGGATCATG GGCCGGGTGCGGTGGCTCACACCTGTAATCCCGGCACTTTGGGAGGCCAAGGCGGGTGGATCATG T C SPPL2A Ensembl:ENSG00000138600 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs938330782 Functional Loss SNV dbSNP153 33..33 33 - - - 44083 RMVar_ID_44083 Human_SNP_ID_577028723 A-to-I Human chr15 - 50703640 50703640 50703640 TATTTGAACTAAGGCCGGGTGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGC TATTTGAACTAAGGCCGGGTGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGC T C SPPL2A Ensembl:ENSG00000138600 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1183463207 Functional Loss SNV dbSNP153 33..33 33 - - - 44084 RMVar_ID_44084 Human_SNP_ID_577028839 A-to-I Human chr15 - 50704160 50704159 50704160 TATAGTATTTTTAGTAGAGACGGGGTTTCTCCATGTTGATCAGGCTGGTCTCGAACTCCCAACCT TATAGTATTTTTAGTAGAGACGGGGTTTCTCC_TGTTGATCAGGCTGGTCTCGAACTCCCAACCT AT A SPPL2A Ensembl:ENSG00000138600 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1187947862 Functional Loss DEL dbSNP153 33..33 33 - - - 44085 RMVar_ID_44085 Human_SNP_ID_577028840 A-to-I Human chr15 - 50704160 50704160 50704160 TATAGTATTTTTAGTAGAGACGGGGTTTCTCCATGTTGATCAGGCTGGTCTCGAACTCCCAACCT TATAGTATTTTTAGTAGAGACGGGGTTTCTCCTTGTTGATCAGGCTGGTCTCGAACTCCCAACCT T A SPPL2A Ensembl:ENSG00000138600 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs990008951 Functional Loss SNV dbSNP153 33..33 33 - - - 44086 RMVar_ID_44086 Human_SNP_ID_577028846 A-to-I Human chr15 - 50704177 50704177 50704177 CCACCACACCCGGCTAATATAGTATTTTTAGTAGAGACGGGGTTTCTCCATGTTGATCAGGCTGG CCACCACACCCGGCTAATATAGTATTTTTAGTGGAGACGGGGTTTCTCCATGTTGATCAGGCTGG T C SPPL2A Ensembl:ENSG00000138600 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs766575082 Functional Loss SNV dbSNP153 33..33 33 - - - 44087 RMVar_ID_44087 Human_SNP_ID_577028872 A-to-I Human chr15 - 50704298 50704298 50704298 CGCTCTTTTTGCCCAGGCTGGAGTGCAATGGCATGATATCAGCTCACTGCAATCTCCGACTCCCG CGCTCTTTTTGCCCAGGCTGGAGTGCAATGGCGTGATATCAGCTCACTGCAATCTCCGACTCCCG T C SPPL2A Ensembl:ENSG00000138600 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1268048396 Functional Loss SNV dbSNP153 33..33 33 - - - 44088 RMVar_ID_44088 Human_SNP_ID_577029354 A-to-I Human chr15 - 50706133 50706133 50706133 CCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCCCGGCCATATCTCAG CCCGCCTCGGCCTCCCAAAGTGCTGGGATTACTGGCGTGAGCCACCGCGCCCGGCCATATCTCAG T A SPPL2A Ensembl:ENSG00000138600 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs541949875 Functional Loss SNV dbSNP153 33..33 33 - - - 44089 RMVar_ID_44089 Human_SNP_ID_577029717 A-to-I Human chr15 - 50707141 50707141 50707141 GCACTCCAGCCTGGGCGACAGAGTGAGACTCCATCCCAAAAAAAAAGATTTATGCAAATTATATC GCACTCCAGCCTGGGCGACAGAGTGAGACTCCGTCCCAAAAAAAAAGATTTATGCAAATTATATC T C SPPL2A Ensembl:ENSG00000138600 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1156818141 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6434171 44090 RMVar_ID_44090 Human_SNP_ID_577029755 A-to-I Human chr15 - 50707288 50707288 50707288 ACGGTGAAACCCCTCTCTACTAAAAATACCAAAAATTAGCTGGGCGTGGTGGAGGGTGCCTGTAG ACGGTGAAACCCCTCTCTACTAAAAATACCAAGAATTAGCTGGGCGTGGTGGAGGGTGCCTGTAG T C SPPL2A Ensembl:ENSG00000138600 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs567357958 Functional Loss SNV dbSNP153 33..33 33 - - - 44091 RMVar_ID_44091 Human_SNP_ID_577029813 A-to-I Human chr15 - 50707412 50707412 50707412 GGTTTTACTGTAAAGAATTATGCAAATTGGCCAGGCGCGGTGGCTCACGCCTGTAATCCCAACAC GGTTTTACTGTAAAGAATTATGCAAATTGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAACAC T C SPPL2A Ensembl:ENSG00000138600 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs575326894 Functional Loss SNV dbSNP153 33..33 33 - - - 44092 RMVar_ID_44092 Human_SNP_ID_577036178 A-to-I Human chr15 - 50732885 50732885 50732885 ACTTGGGAAGCTGAGACATGAAAATCACTTGAACCCAGGAGGTGAAGGTTGCAGTTAGCCGAGAT ACTTGGGAAGCTGAGACATGAAAATCACTTGAGCCCAGGAGGTGAAGGTTGCAGTTAGCCGAGAT T C SPPL2A Ensembl:ENSG00000138600 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs552231962 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_171987,RMVar_hsa_circ_116964,RMVar_hsa_circ_88720,RMVar_hsa_circ_283723,RMVar_hsa_circ_171986,RMVar_hsa_circ_275729,RMVar_hsa_circ_46645,RMVar_hsa_circ_171988,RMVar_hsa_circ_171989,RMVar_hsa_circ_281109,RMVar_hsa_circ_341976,RMVar_hsa_circ_359575,RMVar_hsa_circ_302891,RMVar_hsa_circ_307956,RMVar_hsa_circ_171992,RMVar_hsa_circ_48267,RMVar_hsa_circ_117907,RMVar_hsa_circ_171995,RMVar_hsa_circ_335611,RMVar_hsa_circ_171998,RMVar_hsa_circ_82176,RMVar_hsa_circ_172000,RMVar_hsa_circ_171999,RMVar_hsa_circ_7295,RMVar_hsa_circ_172002,RMVar_hsa_circ_303910,RMVar_hsa_circ_301943,RMVar_hsa_circ_355409,RMVar_hsa_circ_172003 44093 RMVar_ID_44093 Human_SNP_ID_577037476 A-to-I Human chr15 - 50738140 50738140 50738140 CTGCTCTGTCACCCAGGCTGGAGTGCAGTGGCACAATCTGGGTTCACTGCAACCTCTGCCTCTCG CTGCTCTGTCACCCAGGCTGGAGTGCAGTGGCGCAATCTGGGTTCACTGCAACCTCTGCCTCTCG T C SPPL2A Ensembl:ENSG00000138600 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs986363428 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_171987,RMVar_hsa_circ_116964,RMVar_hsa_circ_88720,RMVar_hsa_circ_283723,RMVar_hsa_circ_171986,RMVar_hsa_circ_275729,RMVar_hsa_circ_171988,RMVar_hsa_circ_171989,RMVar_hsa_circ_281109,RMVar_hsa_circ_341976,RMVar_hsa_circ_307956,RMVar_hsa_circ_171992,RMVar_hsa_circ_48267,RMVar_hsa_circ_171995,RMVar_hsa_circ_335611,RMVar_hsa_circ_171998,RMVar_hsa_circ_82176,RMVar_hsa_circ_171999,RMVar_hsa_circ_172002,RMVar_hsa_circ_303910,RMVar_hsa_circ_301943,RMVar_hsa_circ_355409,RMVar_hsa_circ_336523,RMVar_hsa_circ_172003,RMVar_hsa_circ_359164,RMVar_hsa_circ_285808,RMVar_hsa_circ_76470,RMVar_hsa_circ_172004,RMVar_hsa_circ_172005,RMVar_hsa_circ_172006 44094 RMVar_ID_44094 Human_SNP_ID_577074791 A-to-I Human chr15 - 50888933 50888933 50888933 TTGGCTCATTGCAACTTCTGCCTCCCCGGTTCAGGCGATTCTCCTGCCCCAGCCTCCCCAGCTGG TTGGCTCATTGCAACTTCTGCCTCCCCGGTTCGGGCGATTCTCCTGCCCCAGCCTCCCCAGCTGG T C AC021752.1 Ensembl:ENSG00000273674 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs915639583 Functional Loss SNV dbSNP153 33..33 33 - - - 44095 RMVar_ID_44095 Human_SNP_ID_577079272 A-to-I Human chr15 - 50905637 50905637 50905637 AAAAATTTAGCCGGGCATGGTGGCACACCTGTAGTCCCAACTACTTGGGAAGCTGAGGCAGGAGA AAAAATTTAGCCGGGCATGGTGGCACACCTGTGGTCCCAACTACTTGGGAAGCTGAGGCAGGAGA T C AC021752.1 Ensembl:ENSG00000273674 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1405989688 Functional Loss SNV dbSNP153 33..33 33 - - - 44096 RMVar_ID_44096 Human_SNP_ID_577086573 A-to-I Human chr15 + 50932049 50932049 50932049 TTGCCCAGGCTGGAGTGTAGTGGCGCGATCTCAGCTCACTGCAACCTCCACCTCCCGGATTCAAG TTGCCCAGGCTGGAGTGTAGTGGCGCGATCTCGGCTCACTGCAACCTCCACCTCCCGGATTCAAG A G AP4E1 Ensembl:ENSG00000081014 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1282775987 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_340872,RMVar_hsa_circ_356982,RMVar_hsa_circ_325933,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_60468,RMVar_hsa_circ_43699,RMVar_hsa_circ_74890,RMVar_hsa_circ_48840,RMVar_hsa_circ_85453,RMVar_hsa_circ_360028,RMVar_hsa_circ_172016,RMVar_hsa_circ_329212,RMVar_hsa_circ_35121 44097 RMVar_ID_44097 Human_SNP_ID_577089633 A-to-I Human chr15 - 50945757 50945757 50945757 TTTCTAGTTATAATCCTTAGCTGCTTTTTCTCATGATGTAAGCACACCAAATTTTTCAGAAGCAT TTTCTAGTTATAATCCTTAGCTGCTTTTTCTCGTGATGTAAGCACACCAAATTTTTCAGAAGCAT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878899009 Functional Loss SNV dbSNP153 33..33 33 - - - 44098 RMVar_ID_44098 Human_SNP_ID_577214757 A-to-I Human chr15 - 51464338 51464338 51464338 TGGAGAGCAGTGGTGCAATCTCAGCTCACTGCAGCCTCAACCTCCTGGGCTCAACCCATCTTTTT TGGAGAGCAGTGGTGCAATCTCAGCTCACTGCCGCCTCAACCTCCTGGGCTCAACCCATCTTTTT T G DMXL2 Ensembl:ENSG00000104093 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1467025686 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8918,RMVar_hsa_circ_172035,RMVar_hsa_circ_335202,RMVar_hsa_circ_267697,RMVar_hsa_circ_299197,RMVar_hsa_circ_30040,RMVar_hsa_circ_172037,RMVar_hsa_circ_269742,RMVar_hsa_circ_38935,RMVar_hsa_circ_333811,RMVar_hsa_circ_65854,RMVar_hsa_circ_264873,RMVar_hsa_circ_329864,RMVar_hsa_circ_354722,RMVar_hsa_circ_15811 44099 RMVar_ID_44099 Human_SNP_ID_577240025 A-to-I Human chr15 - 51567982 51567982 51567982 GCCTCAACCTGTCAAATGGTCCTCCCACCTCAACCTCCCAAGTAGTTGCGACTATAGGCATGTAC GCCTCAACCTGTCAAATGGTCCTCCCACCTCAGCCTCCCAAGTAGTTGCGACTATAGGCATGTAC T C DMXL2 Ensembl:ENSG00000104093 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1397106190 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_350777,RMVar_hsa_circ_48583,RMVar_hsa_circ_172052,RMVar_hsa_circ_351435,RMVar_hsa_circ_297648,RMVar_hsa_circ_65072,RMVar_hsa_circ_172061,RMVar_hsa_circ_50086,RMVar_hsa_circ_289532,RMVar_hsa_circ_172068 44100 RMVar_ID_44100 Human_SNP_ID_577301511 A-to-I Human chr15 + 51815287 51815287 51815287 TCCATCTCAAAAAATAAAATAAAATATATACTATCTTGCTCCTCAGAACCAGTGGGGAAGAAGAG TCCATCTCAAAAAATAAAATAAAATATATACTGTCTTGCTCCTCAGAACCAGTGGGGAAGAAGAG A G TMOD2 Ensembl:ENSG00000128872 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs190091010 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269082,RMVar_hsa_circ_265861 44101 RMVar_ID_44101 Human_SNP_ID_577306279 A-to-I Human chr15 + 51835518 51835518 51835518 TTTAGTAGAGATGGAGTTTCATCATGTTTCCCAGGCTGTCCTTGAACTCCTGAGCTCAAGCAAAC TTTAGTAGAGATGGAGTTTCATCATGTTTCCCGGGCTGTCCTTGAACTCCTGAGCTCAAGCAAAC A G TMOD3 Ensembl:ENSG00000138594 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1260901378 Functional Loss SNV dbSNP153 33..33 33 - - - 44102 RMVar_ID_44102 Human_SNP_ID_577310339 A-to-I Human chr15 + 51853421 51853421 51853421 GGGGGTCTCACTATGTTGCCCAGGCTCGTCTCAAACTCCTGGACTTAAGCGATCCTCCCTCCTTG GGGGGTCTCACTATGTTGCCCAGGCTCGTCTCGAACTCCTGGACTTAAGCGATCCTCCCTCCTTG A G TMOD3 Ensembl:ENSG00000138594 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1317891386 Functional Loss SNV dbSNP153 33..33 33 - - - 44103 RMVar_ID_44103 Human_SNP_ID_577313065 A-to-I Human chr15 + 51865061 51865061 51865061 CAGGCAAGAGTGAAGTGGTGCAGTGATAGCTCACTGCAGCCTCGAACTTCTGGGCTCAAGCGATC CAGGCAAGAGTGAAGTGGTGCAGTGATAGCTCGCTGCAGCCTCGAACTTCTGGGCTCAAGCGATC A G TMOD3 Ensembl:ENSG00000138594 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs963463603 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17960,RMVar_hsa_circ_313923,RMVar_hsa_circ_172094,RMVar_hsa_circ_172095 44104 RMVar_ID_44104 Human_SNP_ID_577316050 A-to-I Human chr15 + 51876916 51876916 51876916 GACCGTGCCTCTACTAAAAATGAAAAAAAGTTAGCTGGATGCGGTGGTGTGTGCCTGTAGTTCCA GACCGTGCCTCTACTAAAAATGAAAAAAAGTTTGCTGGATGCGGTGGTGTGTGCCTGTAGTTCCA A T TMOD3 Ensembl:ENSG00000138594 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404762096 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120578,RMVar_hsa_circ_17960,RMVar_hsa_circ_308985,RMVar_hsa_circ_172094,RMVar_hsa_circ_311046,RMVar_hsa_circ_338683,RMVar_hsa_circ_284949,RMVar_hsa_circ_123464,RMVar_hsa_circ_172098,RMVar_hsa_circ_172100,RMVar_hsa_circ_172102,RMVar_hsa_circ_77990,RMVar_hsa_circ_172101,RMVar_hsa_circ_172099,RMVar_hsa_circ_172097 44105 RMVar_ID_44105 Human_SNP_ID_577324951 A-to-I Human chr15 + 51910343 51910343 51910343 ACGCCTGTAATCCCAGCACTTTTGGGAAGCCAAAGTGGGTGGATCACTTAAGGTCAGGAGTTCAA ACGCCTGTAATCCCAGCACTTTTGGGAAGCCAGAGTGGGTGGATCACTTAAGGTCAGGAGTTCAA A G TMOD3 Ensembl:ENSG00000138594 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1278077030 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_458931,Human_RBP_ID_6435022,Human_RBP_ID_12655207,Human_RBP_ID_22388027 RMVar_hsa_circ_172102,RMVar_hsa_circ_77990,RMVar_hsa_circ_49349,RMVar_hsa_circ_3421,RMVar_hsa_circ_172105,RMVar_hsa_circ_98659,RMVar_hsa_circ_33175,RMVar_hsa_circ_28596 44106 RMVar_ID_44106 Human_SNP_ID_577325429 A-to-I Human chr15 + 51912266 51912266 51912266 CCTGACCAACATGGAGAAACCCTGTCTCTACTAAAAATACAAAATTAGCCAGGCGTGGTGGCACA CCTGACCAACATGGAGAAACCCTGTCTCTACTGAAAATACAAAATTAGCCAGGCGTGGTGGCACA A G TMOD3 Ensembl:ENSG00000138594 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1222023086 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172105,RMVar_hsa_circ_98659,RMVar_hsa_circ_172111,RMVar_hsa_circ_28596,RMVar_hsa_circ_172110 44107 RMVar_ID_44107 Human_SNP_ID_577325453 A-to-I Human chr15 + 51912345 51912345 51912345 GCTACTCGGGAGGCTGAGGCAGGAGAATCACTAGAACTCGGGAGGCGGAGGTTGCAGTTAGCTGA GCTACTCGGGAGGCTGAGGCAGGAGAATCACTGGAACTCGGGAGGCGGAGGTTGCAGTTAGCTGA A G TMOD3 Ensembl:ENSG00000138594 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1234847338 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172105,RMVar_hsa_circ_98659,RMVar_hsa_circ_172111,RMVar_hsa_circ_28596,RMVar_hsa_circ_172110 44108 RMVar_ID_44108 Human_SNP_ID_577325653 A-to-I Human chr15 + 51913196 51913196 51913196 GGGGTTTCACCATGTTGGCCGGGCTGTTCTCAAAGTGACCTCAGGTGATCCACTCGCCTCGGCCT GGGGTTTCACCATGTTGGCCGGGCTGTTCTCACAGTGACCTCAGGTGATCCACTCGCCTCGGCCT A C TMOD3 Ensembl:ENSG00000138594 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs987999664 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2506635,Human_miRNA_ID_2515003,Human_miRNA_ID_3043206 RMVar_hsa_circ_172105,RMVar_hsa_circ_98659,RMVar_hsa_circ_172111,RMVar_hsa_circ_28596,RMVar_hsa_circ_172110 44109 RMVar_ID_44109 Human_SNP_ID_577325654 A-to-I Human chr15 + 51913211 51913211 51913211 TGGCCGGGCTGTTCTCAAAGTGACCTCAGGTGATCCACTCGCCTCGGCCTCCCAAAGTGCTGGGA TGGCCGGGCTGTTCTCAAAGTGACCTCAGGTGGTCCACTCGCCTCGGCCTCCCAAAGTGCTGGGA A G TMOD3 Ensembl:ENSG00000138594 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1297416099 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2506635,Human_miRNA_ID_3043206 RMVar_hsa_circ_172105,RMVar_hsa_circ_98659,RMVar_hsa_circ_172111,RMVar_hsa_circ_28596,RMVar_hsa_circ_172110 44110 RMVar_ID_44110 Human_SNP_ID_577325797 A-to-I Human chr15 + 51913817 51913817 51913817 GACGGATCACTTGAGCTCAGGAGTTTGAGACCAACCTGCGTAACATGGTGAAACCCCATATCTAC GACGGATCACTTGAGCTCAGGAGTTTGAGACCGACCTGCGTAACATGGTGAAACCCCATATCTAC A G TMOD3 Ensembl:ENSG00000138594 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs550929192 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27435566 RMVar_hsa_circ_172105,RMVar_hsa_circ_98659,RMVar_hsa_circ_172111,RMVar_hsa_circ_28596,RMVar_hsa_circ_172110 44111 RMVar_ID_44111 Human_SNP_ID_577325845 A-to-I Human chr15 + 51914002 51914002 51914002 GCTGCTGTACTCTAGCCTGGGCAATGAGAGTGAAACTCTTATCTCAAAAAAAAAAAAAAAAAAAG GCTGCTGTACTCTAGCCTGGGCAATGAGAGTGGAACTCTTATCTCAAAAAAAAAAAAAAAAAAAG A G TMOD3 Ensembl:ENSG00000138594 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs111819357 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172105,RMVar_hsa_circ_98659,RMVar_hsa_circ_172111,RMVar_hsa_circ_28596,RMVar_hsa_circ_172110 44112 RMVar_ID_44112 Human_SNP_ID_577325900 A-to-I Human chr15 + 51914178 51914178 51914178 AATTAGCCAGACACCTATAGTACCAGCTACTTAGGAGTCTAAAGTGGGAGAATTGCTTGAGCCTG AATTAGCCAGACACCTATAGTACCAGCTACTTCGGAGTCTAAAGTGGGAGAATTGCTTGAGCCTG A C TMOD3 Ensembl:ENSG00000138594 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs527449717 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172105,RMVar_hsa_circ_98659,RMVar_hsa_circ_172111,RMVar_hsa_circ_28596,RMVar_hsa_circ_172110 44113 RMVar_ID_44113 Human_SNP_ID_577325901 A-to-I Human chr15 + 51914178 51914178 51914178 AATTAGCCAGACACCTATAGTACCAGCTACTTAGGAGTCTAAAGTGGGAGAATTGCTTGAGCCTG AATTAGCCAGACACCTATAGTACCAGCTACTTGGGAGTCTAAAGTGGGAGAATTGCTTGAGCCTG A G TMOD3 Ensembl:ENSG00000138594 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs527449717 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172105,RMVar_hsa_circ_98659,RMVar_hsa_circ_172111,RMVar_hsa_circ_28596,RMVar_hsa_circ_172110 44114 RMVar_ID_44114 Human_SNP_ID_577325909 A-to-I Human chr15 + 51914230 51914230 51914230 TTGCTTGAGCCTGGGAGGTTGAAGCAGCAGTGAGCTTTGATCATGCCACTGCATTCCAGCCTGGG TTGCTTGAGCCTGGGAGGTTGAAGCAGCAGTGTGCTTTGATCATGCCACTGCATTCCAGCCTGGG A T TMOD3 Ensembl:ENSG00000138594 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1245024905 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12527856 RMVar_hsa_circ_172105,RMVar_hsa_circ_98659,RMVar_hsa_circ_172111,RMVar_hsa_circ_28596,RMVar_hsa_circ_172110 44115 RMVar_ID_44115 Human_SNP_ID_577325923 A-to-I Human chr15 + 51914288 51914288 51914288 GCCTGGGTAACAAGAGTGAGACTGTCTCAAAAAACAAAACAAAACAAAAAAATGGGTTTTTTTGT GCCTGGGTAACAAGAGTGAGACTGTCTCAAAAGACAAAACAAAACAAAAAAATGGGTTTTTTTGT A G TMOD3 Ensembl:ENSG00000138594 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs538132626 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172105,RMVar_hsa_circ_98659,RMVar_hsa_circ_172111,RMVar_hsa_circ_28596,RMVar_hsa_circ_172110 44116 RMVar_ID_44116 Human_SNP_ID_577325971 A-to-I Human chr15 + 51914460 51914460 51914460 CTGAGGTGGGCGGATCACTTGAGGTCAGGAGTACGAGACCAGTCTGGCCAACATGGTGAAACCCC CTGAGGTGGGCGGATCACTTGAGGTCAGGAGTTCGAGACCAGTCTGGCCAACATGGTGAAACCCC A T TMOD3 Ensembl:ENSG00000138594 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1316786681 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172105,RMVar_hsa_circ_98659,RMVar_hsa_circ_172111,RMVar_hsa_circ_28596,RMVar_hsa_circ_172110 44117 RMVar_ID_44117 Human_SNP_ID_577325982 A-to-I Human chr15 + 51914502 51914502 51914502 TCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAAATTAGTTGGGCGTGGTGATG TCTGGCCAACATGGTGAAACCCCATCTCTACTGAAAATACAAAAAATTAGTTGGGCGTGGTGATG A G TMOD3 Ensembl:ENSG00000138594 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1419183129 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172105,RMVar_hsa_circ_98659,RMVar_hsa_circ_172111,RMVar_hsa_circ_28596,RMVar_hsa_circ_172110 44118 RMVar_ID_44118 Human_SNP_ID_577325999 A-to-I Human chr15 + 51914566 51914566 51914566 GCGCACCTGTAATTCTAGCTACTTGGGAGCCTAAGGCAGGAGAATCACTTGAACCTGGGAGGCAG GCGCACCTGTAATTCTAGCTACTTGGGAGCCTGAGGCAGGAGAATCACTTGAACCTGGGAGGCAG A G TMOD3 Ensembl:ENSG00000138594 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs753510950 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172105,RMVar_hsa_circ_98659,RMVar_hsa_circ_172111,RMVar_hsa_circ_28596,RMVar_hsa_circ_172110 44119 RMVar_ID_44119 Human_SNP_ID_577326056 A-to-I Human chr15 + 51914806 51914806 51914806 CAGGCTGGAGCGCAATGGTGCGATCTCAGCTCACTGCAACCTCCGCCTCCTGGGTTCAGATGATT CAGGCTGGAGCGCAATGGTGCGATCTCAGCTCTCTGCAACCTCCGCCTCCTGGGTTCAGATGATT A T TMOD3 Ensembl:ENSG00000138594 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1033750561 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172105,RMVar_hsa_circ_98659,RMVar_hsa_circ_172111,RMVar_hsa_circ_28596,RMVar_hsa_circ_172110 44120 RMVar_ID_44120 Human_SNP_ID_577326062 A-to-I Human chr15 + 51914849 51914817 51914849 CGCCTCCTGGGTTCAGATGATTTTCCTGCCTCAGCCTCCTGGGTAGCTGGGACTACAGGTGCCCG C________________________________GCCTCCTGGGTAGCTGGGACTACAGGTGCCCG CGCCTCCTGGGTTCAGATGATTTTCCTGCCTCA C TMOD3 Ensembl:ENSG00000138594 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs995548003 Functional Loss DEL dbSNP153 2..33 33 - - - RMVar_hsa_circ_172105,RMVar_hsa_circ_98659,RMVar_hsa_circ_172111,RMVar_hsa_circ_28596,RMVar_hsa_circ_172110 44121 RMVar_ID_44121 Human_SNP_ID_577326069 A-to-I Human chr15 + 51914871 51914871 51914871 TTCCTGCCTCAGCCTCCTGGGTAGCTGGGACTACAGGTGCCCGCCACCACGCCTGACTAATTTTT TTCCTGCCTCAGCCTCCTGGGTAGCTGGGACTTCAGGTGCCCGCCACCACGCCTGACTAATTTTT A T TMOD3 Ensembl:ENSG00000138594 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs989343103 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172105,RMVar_hsa_circ_98659,RMVar_hsa_circ_172111,RMVar_hsa_circ_28596,RMVar_hsa_circ_172110 44122 RMVar_ID_44122 Human_SNP_ID_577326106 A-to-I Human chr15 + 51914968 51914968 51914968 TGGCCAGGCTGGTCTCGAACTCCTGACCTCGTAATCCACCCGCCTCGGCCTCCCAAAGTGCTGGG TGGCCAGGCTGGTCTCGAACTCCTGACCTCGTGATCCACCCGCCTCGGCCTCCCAAAGTGCTGGG A G TMOD3 Ensembl:ENSG00000138594 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs930253096 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172105,RMVar_hsa_circ_98659,RMVar_hsa_circ_172111,RMVar_hsa_circ_28596,RMVar_hsa_circ_172110 44123 RMVar_ID_44123 Human_SNP_ID_577330462 A-to-I Human chr15 + 51932695 51932695 51932695 CTCCTGCCTCAGCCTCCGTAGCAGCTGGGATTACAGGCACCTGCCACCACACACAGCTAATTTTT CTCCTGCCTCAGCCTCCGTAGCAGCTGGGATTCCAGGCACCTGCCACCACACACAGCTAATTTTT A C TMOD3 Ensembl:ENSG00000138594 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs938193775 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172111,RMVar_hsa_circ_172110,RMVar_hsa_circ_172112 44124 RMVar_ID_44124 Human_SNP_ID_577330887 A-to-I Human chr15 + 51934527 51934527 51934527 TATTAATATGGAGGGGAAAAAAGCATTTGCCCAGGCTGGTCTTGAACTCCTGACCTCAGGTGATC TATTAATATGGAGGGGAAAAAAGCATTTGCCCGGGCTGGTCTTGAACTCCTGACCTCAGGTGATC A G TMOD3 Ensembl:ENSG00000138594 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1451361972 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172111 44125 RMVar_ID_44125 Human_SNP_ID_577341776 A-to-I Human chr15 + 51976823 51976823 51976823 AAATTAGCCGGGCTTGGCGGTCGCACTCCTGTAATCTCAGCTACTCAGGAAGCTGAAGCAGGAGA AAATTAGCCGGGCTTGGCGGTCGCACTCCTGTGATCTCAGCTACTCAGGAAGCTGAAGCAGGAGA A G MAPK6 Ensembl:ENSG00000069956 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1305262750 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172111 44126 RMVar_ID_44126 Human_SNP_ID_577341780 A-to-I Human chr15 + 51976833 51976833 51976833 GGCTTGGCGGTCGCACTCCTGTAATCTCAGCTACTCAGGAAGCTGAAGCAGGAGAATCGCTTCAA GGCTTGGCGGTCGCACTCCTGTAATCTCAGCTGCTCAGGAAGCTGAAGCAGGAGAATCGCTTCAA A G MAPK6 Ensembl:ENSG00000069956 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs953590021 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172111 44127 RMVar_ID_44127 Human_SNP_ID_577341781 A-to-I Human chr15 + 51976833 51976833 51976833 GGCTTGGCGGTCGCACTCCTGTAATCTCAGCTACTCAGGAAGCTGAAGCAGGAGAATCGCTTCAA GGCTTGGCGGTCGCACTCCTGTAATCTCAGCTTCTCAGGAAGCTGAAGCAGGAGAATCGCTTCAA A T MAPK6 Ensembl:ENSG00000069956 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs953590021 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172111 44128 RMVar_ID_44128 Human_SNP_ID_577354422 A-to-I Human chr15 + 52022340 52022340 52022340 TGGAGTGTAGTGGTGCGATCACTGTTCACTGCAACCTCTACTTCCCGGGCTCAGGTGATCTTCCT TGGAGTGTAGTGGTGCGATCACTGTTCACTGCGACCTCTACTTCCCGGGCTCAGGTGATCTTCCT A G MAPK6 Ensembl:ENSG00000069956 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs532885495 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172121,RMVar_hsa_circ_95351,RMVar_hsa_circ_104754,RMVar_hsa_circ_172122 44129 RMVar_ID_44129 Human_SNP_ID_577356297 A-to-I Human chr15 + 52027804 52027804 52027804 TATTTATTTACTGTTTTTTGAGATGGAGTCTCACTCTGTTGGCCAGGTTGGAGTGCAGTGGCACG TATTTATTTACTGTTTTTTGAGATGGAGTCTCCCTCTGTTGGCCAGGTTGGAGTGCAGTGGCACG A C MAPK6 Ensembl:ENSG00000069956 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1248900062 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12651820 Human_Splice_Rec_1602989 RMVar_hsa_circ_172121,RMVar_hsa_circ_95351,RMVar_hsa_circ_104754,RMVar_hsa_circ_172122 44130 RMVar_ID_44130 Human_SNP_ID_577359580 A-to-I Human chr15 + 52038998 52038998 52038998 AGTTTATCTGGTCTATGAATTTTTGAATTTCTAATATGAATGGGTTACAGTAAATCTGTAACTAG AGTTTATCTGGTCTATGAATTTTTGAATTTCTCATATGAATGGGTTACAGTAAATCTGTAACTAG A C MAPK6 Ensembl:ENSG00000069956 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1337889540 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172121,RMVar_hsa_circ_95351,RMVar_hsa_circ_104754,RMVar_hsa_circ_172122 44131 RMVar_ID_44131 Human_SNP_ID_577360699 A-to-I Human chr15 + 52043095 52043095 52043095 CAGAGGTTGCAGTGAGTGGTGATCACGCCACTACACTCTGGCCTGGATGACAGAGCAATACCCTG CAGAGGTTGCAGTGAGTGGTGATCACGCCACTGCACTCTGGCCTGGATGACAGAGCAATACCCTG A G MAPK6 Ensembl:ENSG00000069956 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1363160699 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17563202 RMVar_hsa_circ_172121,RMVar_hsa_circ_95351,RMVar_hsa_circ_104754,RMVar_hsa_circ_172122 44132 RMVar_ID_44132 Human_SNP_ID_577363010 A-to-I Human chr15 + 52051097 52051097 52051097 TTTTTTTTTCTGAGACGGAGTCTTGCTCTGTCACCCAGGCTGGAGTGCAGTGGTGCGATTTCTGC TTTTTTTTTCTGAGACGGAGTCTTGCTCTGTCGCCCAGGCTGGAGTGCAGTGGTGCGATTTCTGC A G MAPK6 Ensembl:ENSG00000069956 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1322095665 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9053315 RMVar_hsa_circ_172121,RMVar_hsa_circ_95351,RMVar_hsa_circ_104754,RMVar_hsa_circ_172122,RMVar_hsa_circ_93977,RMVar_hsa_circ_172124,RMVar_hsa_circ_89730,RMVar_hsa_circ_341010,RMVar_hsa_circ_376238,RMVar_hsa_circ_172125,RMVar_hsa_circ_336183,RMVar_hsa_circ_332923,RMVar_hsa_circ_172127,RMVar_hsa_circ_172126 44133 RMVar_ID_44133 Human_SNP_ID_577363075 A-to-I Human chr15 + 52051233 52051233 52051233 GCGCCCGCCCCGTCGCCCGGCTAATTTTTTGTATTTTTAGTGGAGATAGGGTTTTACCATGTTAG GCGCCCGCCCCGTCGCCCGGCTAATTTTTTGTGTTTTTAGTGGAGATAGGGTTTTACCATGTTAG A G MAPK6 Ensembl:ENSG00000069956 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1288869154 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172121,RMVar_hsa_circ_95351,RMVar_hsa_circ_104754,RMVar_hsa_circ_172122,RMVar_hsa_circ_93977,RMVar_hsa_circ_172124,RMVar_hsa_circ_89730,RMVar_hsa_circ_341010,RMVar_hsa_circ_376238,RMVar_hsa_circ_172125,RMVar_hsa_circ_336183,RMVar_hsa_circ_332923,RMVar_hsa_circ_172127,RMVar_hsa_circ_172126 44134 RMVar_ID_44134 Human_SNP_ID_577363109 A-to-I Human chr15 + 52051317 52051317 52051317 CTGACCTCGTGATCCACCCGCCTCGGCCTCCCAAAGTACTGGGATTACAGGCGTGAGCCACCCCA CTGACCTCGTGATCCACCCGCCTCGGCCTCCCGAAGTACTGGGATTACAGGCGTGAGCCACCCCA A G MAPK6 Ensembl:ENSG00000069956 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1276168762 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172121,RMVar_hsa_circ_95351,RMVar_hsa_circ_104754,RMVar_hsa_circ_172122,RMVar_hsa_circ_93977,RMVar_hsa_circ_172124,RMVar_hsa_circ_89730,RMVar_hsa_circ_341010,RMVar_hsa_circ_376238,RMVar_hsa_circ_172125,RMVar_hsa_circ_336183,RMVar_hsa_circ_332923,RMVar_hsa_circ_172127,RMVar_hsa_circ_172126 44135 RMVar_ID_44135 Human_SNP_ID_577363111 A-to-I Human chr15 + 52051322 52051322 52051322 CTCGTGATCCACCCGCCTCGGCCTCCCAAAGTACTGGGATTACAGGCGTGAGCCACCCCACCAGG CTCGTGATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCCCACCAGG A G MAPK6 Ensembl:ENSG00000069956 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs917553587 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172121,RMVar_hsa_circ_95351,RMVar_hsa_circ_104754,RMVar_hsa_circ_172122,RMVar_hsa_circ_93977,RMVar_hsa_circ_172124,RMVar_hsa_circ_89730,RMVar_hsa_circ_341010,RMVar_hsa_circ_376238,RMVar_hsa_circ_172125,RMVar_hsa_circ_336183,RMVar_hsa_circ_332923,RMVar_hsa_circ_172127,RMVar_hsa_circ_172126 44136 RMVar_ID_44136 Human_SNP_ID_577363677 A-to-I Human chr15 + 52053173 52053173 52053173 TGGCTCACTGCAACCACTGCCACCCAGGTTCAAACAGTTCTCCTGCTCTCAGCCTCCCGAGTAGC TGGCTCACTGCAACCACTGCCACCCAGGTTCACACAGTTCTCCTGCTCTCAGCCTCCCGAGTAGC A C MAPK6 Ensembl:ENSG00000069956 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs545633514 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23655390 RMVar_hsa_circ_172121,RMVar_hsa_circ_95351,RMVar_hsa_circ_104754,RMVar_hsa_circ_172122,RMVar_hsa_circ_93977,RMVar_hsa_circ_172124,RMVar_hsa_circ_89730,RMVar_hsa_circ_341010,RMVar_hsa_circ_376238,RMVar_hsa_circ_172125,RMVar_hsa_circ_336183,RMVar_hsa_circ_332923,RMVar_hsa_circ_172127,RMVar_hsa_circ_172126 44137 RMVar_ID_44137 Human_SNP_ID_577363678 A-to-I Human chr15 + 52053173 52053173 52053173 TGGCTCACTGCAACCACTGCCACCCAGGTTCAAACAGTTCTCCTGCTCTCAGCCTCCCGAGTAGC TGGCTCACTGCAACCACTGCCACCCAGGTTCAGACAGTTCTCCTGCTCTCAGCCTCCCGAGTAGC A G MAPK6 Ensembl:ENSG00000069956 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs545633514 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23655390 RMVar_hsa_circ_172121,RMVar_hsa_circ_95351,RMVar_hsa_circ_104754,RMVar_hsa_circ_172122,RMVar_hsa_circ_93977,RMVar_hsa_circ_172124,RMVar_hsa_circ_89730,RMVar_hsa_circ_341010,RMVar_hsa_circ_376238,RMVar_hsa_circ_172125,RMVar_hsa_circ_336183,RMVar_hsa_circ_332923,RMVar_hsa_circ_172127,RMVar_hsa_circ_172126 44138 RMVar_ID_44138 Human_SNP_ID_577363924 A-to-I Human chr15 + 52053823 52053823 52053823 CACTATGCCCAGCTGATTTTTGTATTTTTAGTAGAGACGGGGTTCACCACGTTGGTCAGGCTGAT CACTATGCCCAGCTGATTTTTGTATTTTTAGTGGAGACGGGGTTCACCACGTTGGTCAGGCTGAT A G MAPK6 Ensembl:ENSG00000069956 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1475520841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12528532 RMVar_hsa_circ_172121,RMVar_hsa_circ_95351,RMVar_hsa_circ_104754,RMVar_hsa_circ_172122,RMVar_hsa_circ_93977,RMVar_hsa_circ_172124,RMVar_hsa_circ_89730,RMVar_hsa_circ_341010,RMVar_hsa_circ_376238,RMVar_hsa_circ_172125,RMVar_hsa_circ_336183,RMVar_hsa_circ_332923,RMVar_hsa_circ_172127,RMVar_hsa_circ_172126 44139 RMVar_ID_44139 Human_SNP_ID_577364672 A-to-I Human chr15 + 52055718 52055718 52055718 TTGAAATTTTAGTAGAGACAGGATTTCACCATATTGGTCAGGTTGGTGTTGAACTCCTGACCTCA TTGAAATTTTAGTAGAGACAGGATTTCACCATGTTGGTCAGGTTGGTGTTGAACTCCTGACCTCA A G MAPK6 Ensembl:ENSG00000069956 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs902036104 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172121,RMVar_hsa_circ_95351,RMVar_hsa_circ_104754,RMVar_hsa_circ_172122,RMVar_hsa_circ_93977,RMVar_hsa_circ_172124,RMVar_hsa_circ_89730,RMVar_hsa_circ_341010,RMVar_hsa_circ_376238,RMVar_hsa_circ_172125,RMVar_hsa_circ_336183,RMVar_hsa_circ_332923,RMVar_hsa_circ_172127,RMVar_hsa_circ_172126 44140 RMVar_ID_44140 Human_SNP_ID_577366605 A-to-I Human chr15 - 52061636 52061633 52061637 GCTAGGACTACAGGCGCCTGCCACCACACCTGACTAATTTTTGTATCTTTACATTACTAAATTTT GCTAGGACTACAGGCGCCTGCCACCACACCT____AATTTTTGTATCTTTACATTACTAAATTTT TAGTC T AC023906.5 Ensembl:ENSG00000259712 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348178796 Functional Loss DEL dbSNP153 32..35 33 - - - 44141 RMVar_ID_44141 Human_SNP_ID_577370632 A-to-I Human chr15 + 52073919 52073919 52073919 CCATGACCTCCCACAGTGCTGAGATTACAGGCATGAGCTATCATGACCGGCCTACTACTTCCCTC CCATGACCTCCCACAGTGCTGAGATTACAGGCGTGAGCTATCATGACCGGCCTACTACTTCCCTC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006051209 Functional Loss SNV dbSNP153 33..33 33 - - - 44142 RMVar_ID_44142 Human_SNP_ID_577370633 A-to-I Human chr15 + 52073919 52073919 52073919 CCATGACCTCCCACAGTGCTGAGATTACAGGCATGAGCTATCATGACCGGCCTACTACTTCCCTC CCATGACCTCCCACAGTGCTGAGATTACAGGCTTGAGCTATCATGACCGGCCTACTACTTCCCTC A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006051209 Functional Loss SNV dbSNP153 33..33 33 - - - 44143 RMVar_ID_44143 Human_SNP_ID_577377155 A-to-I Human chr15 + 52095590 52095590 52095590 CTACCATTTAATTAAGAAAGCAGTTGCTGTTCAAAAGCATCTTGAGAGGAACAGAAAGGATAAGA CTACCATTTAATTAAGAAAGCAGTTGCTGTTCGAAAGCATCTTGAGAGGAACAGAAAGGATAAGA A G AC023906.1 Ensembl:ENSG00000242327 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878937830 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1853133,Human_miRNA_ID_1886516,Human_miRNA_ID_1886953 44144 RMVar_ID_44144 Human_SNP_ID_577377158 A-to-I Human chr15 + 52095596 52095596 52095596 TTTAATTAAGAAAGCAGTTGCTGTTCAAAAGCATCTTGAGAGGAACAGAAAGGATAAGAATGCTA TTTAATTAAGAAAGCAGTTGCTGTTCAAAAGCGTCTTGAGAGGAACAGAAAGGATAAGAATGCTA A G AC023906.1 Ensembl:ENSG00000242327 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs927560002 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1853133,Human_miRNA_ID_1886516,Human_miRNA_ID_1886953 44145 RMVar_ID_44145 Human_SNP_ID_577377168 A-to-I Human chr15 + 52095635 52095635 52095635 GAGGAACAGAAAGGATAAGAATGCTAAATTCCATCTGATTCTGATAGAGAGCTGGATTCACCACT GAGGAACAGAAAGGATAAGAATGCTAAATTCCGTCTGATTCTGATAGAGAGCTGGATTCACCACT A G AC023906.1 Ensembl:ENSG00000242327 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879070529 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1840494,Human_miRNA_ID_1861737 44146 RMVar_ID_44146 Human_SNP_ID_577384025 A-to-I Human chr15 - 52118647 52118647 52118647 TCACACTGGTCTCGAACTCCCAACCTCAGGTGATCCTCCCACCTTGGCCTCCCAAAGTGCTGGGA TCACACTGGTCTCGAACTCCCAACCTCAGGTGTTCCTCCCACCTTGGCCTCCCAAAGTGCTGGGA T A GNB5 Ensembl:ENSG00000069966 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053282715 Functional Loss SNV dbSNP153 33..33 33 - - - 44147 RMVar_ID_44147 Human_SNP_ID_577384039 A-to-I Human chr15 - 52118703 52118703 52118703 CCACCACGCCCGGCTAATTTTGTATTTTTAGTAGAGACCAGGTTTCTCCATGTTGGTCACACTGG CCACCACGCCCGGCTAATTTTGTATTTTTAGTGGAGACCAGGTTTCTCCATGTTGGTCACACTGG T C GNB5 Ensembl:ENSG00000069966 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1280146904 Functional Loss SNV dbSNP153 33..33 33 - - - 44148 RMVar_ID_44148 Human_SNP_ID_577384042 A-to-I Human chr15 - 52118712 52118712 52118712 AGGCATGCACCACCACGCCCGGCTAATTTTGTATTTTTAGTAGAGACCAGGTTTCTCCATGTTGG AGGCATGCACCACCACGCCCGGCTAATTTTGTGTTTTTAGTAGAGACCAGGTTTCTCCATGTTGG T C GNB5 Ensembl:ENSG00000069966 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900522706 Functional Loss SNV dbSNP153 33..33 33 - - - 44149 RMVar_ID_44149 Human_SNP_ID_577391176 A-to-I Human chr15 - 52145558 52145558 52145558 TCTCTGCAACCTCCGCTCCCTGGGTTCAAGCAATTCTTCTGCCTCAGCCTCCCAAGTAGCTGGGA TCTCTGCAACCTCCGCTCCCTGGGTTCAAGCAGTTCTTCTGCCTCAGCCTCCCAAGTAGCTGGGA T C GNB5 Ensembl:ENSG00000069966 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1045852421 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114898,RMVar_hsa_circ_48640,RMVar_hsa_circ_172137,RMVar_hsa_circ_291631,RMVar_hsa_circ_172134,RMVar_hsa_circ_311088,RMVar_hsa_circ_286644,RMVar_hsa_circ_172135,RMVar_hsa_circ_172136 44150 RMVar_ID_44150 Human_SNP_ID_577391177 A-to-I Human chr15 - 52145562 52145562 52145562 CGGCTCTCTGCAACCTCCGCTCCCTGGGTTCAAGCAATTCTTCTGCCTCAGCCTCCCAAGTAGCT CGGCTCTCTGCAACCTCCGCTCCCTGGGTTCAGGCAATTCTTCTGCCTCAGCCTCCCAAGTAGCT T C GNB5 Ensembl:ENSG00000069966 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1310957711 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114898,RMVar_hsa_circ_48640,RMVar_hsa_circ_172137,RMVar_hsa_circ_291631,RMVar_hsa_circ_172134,RMVar_hsa_circ_311088,RMVar_hsa_circ_286644,RMVar_hsa_circ_172135,RMVar_hsa_circ_172136 44151 RMVar_ID_44151 Human_SNP_ID_577392805 A-to-I Human chr15 - 52151858 52151858 52151858 CGAGTGATCCTCCTGCCTCAGCCTCTGAAAGCACTGAGATTATAGATGTGAGCCACCTTGCCCTG CGAGTGATCCTCCTGCCTCAGCCTCTGAAAGCGCTGAGATTATAGATGTGAGCCACCTTGCCCTG T C GNB5 Ensembl:ENSG00000069966 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1039603022 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79,RMVar_hsa_circ_114898,RMVar_hsa_circ_48640,RMVar_hsa_circ_172134,RMVar_hsa_circ_311088,RMVar_hsa_circ_172135 44152 RMVar_ID_44152 Human_SNP_ID_577412237 A-to-I Human chr15 - 52229562 52229562 52229562 TGAAGTGCAGTGGCACGATCTCAGCTCACTGCAGCCTGGACCTCCTGGGCTCAAGCGATTCATCC TGAAGTGCAGTGGCACGATCTCAGCTCACTGCTGCCTGGACCTCCTGGGCTCAAGCGATTCATCC T A MYO5C Ensembl:ENSG00000128833 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886731946 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 44153 RMVar_ID_44153 Human_SNP_ID_577414992 A-to-I Human chr15 - 52239850 52239850 52239850 AAGATGCTGGAGGAACATAAGGCTGTGATCCTACAGAAATACGCACGGGCGTGGCTGGCCAGACG AAGATGCTGGAGGAACATAAGGCTGTGATCCTGCAGAAATACGCACGGGCGTGGCTGGCCAGACG T C MYO5C Ensembl:ENSG00000128833 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1433524221 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9371587,Human_RBP_ID_17862004,Human_RBP_ID_25145325 Human_Splice_Rec_1603190,Human_Splice_Rec_1603266,Human_Splice_Rec_1603356 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_62856,RMVar_hsa_circ_267082,RMVar_hsa_circ_172143,RMVar_hsa_circ_56659,RMVar_hsa_circ_265800 44154 RMVar_ID_44154 Human_SNP_ID_577415578 A-to-I Human chr15 - 52241877 52241877 52241877 TCCAGGTGCTGTGGCTCATGCCTGTAGTCCCAACTACTCAGGGAGCTGAAATGGGAGGGTTCCTT TCCAGGTGCTGTGGCTCATGCCTGTAGTCCCAGCTACTCAGGGAGCTGAAATGGGAGGGTTCCTT T C MYO5C Ensembl:ENSG00000128833 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1023510347 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1548,RMVar_hsa_circ_70197,RMVar_hsa_circ_104965,RMVar_hsa_circ_172142,RMVar_hsa_circ_62856,RMVar_hsa_circ_56659,RMVar_hsa_circ_265800 44155 RMVar_ID_44155 Human_SNP_ID_577449590 A-to-I Human chr15 - 52377725 52377725 52377725 CTCCACTAAAAATACAAAAATTAGCTGGACGTAGTGGTGTTTACCTGTAATCCCAGCTACTCAGG CTCCACTAAAAATACAAAAATTAGCTGGACGTGGTGGTGTTTACCTGTAATCCCAGCTACTCAGG T C MYO5A Ensembl:ENSG00000197535 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs12914548 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97707,RMVar_hsa_circ_172150,RMVar_hsa_circ_119422,RMVar_hsa_circ_96945,RMVar_hsa_circ_64037,RMVar_hsa_circ_172153,RMVar_hsa_circ_172154,RMVar_hsa_circ_27808,RMVar_hsa_circ_27761,RMVar_hsa_circ_88272,RMVar_hsa_circ_36741,RMVar_hsa_circ_37856,RMVar_hsa_circ_172157,RMVar_hsa_circ_104238,RMVar_hsa_circ_51057,RMVar_hsa_circ_72503,RMVar_hsa_circ_26927,RMVar_hsa_circ_172158,RMVar_hsa_circ_309897,RMVar_hsa_circ_339583,RMVar_hsa_circ_375907,RMVar_hsa_circ_172160,RMVar_hsa_circ_348159,RMVar_hsa_circ_289030,RMVar_hsa_circ_172161,RMVar_hsa_circ_172162,RMVar_hsa_circ_172163 44156 RMVar_ID_44156 Human_SNP_ID_577450281 A-to-I Human chr15 - 52380087 52380087 52380087 ATGTTTACAGCTCTTTATTTTTACTGCTTATCATCTCCTCCCCATTCTCTCATAGTTTTCCATTT ATGTTTACAGCTCTTTATTTTTACTGCTTATCGTCTCCTCCCCATTCTCTCATAGTTTTCCATTT T C MYO5A Ensembl:ENSG00000197535 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4238391 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5013 RMVar_hsa_circ_97707,RMVar_hsa_circ_172150,RMVar_hsa_circ_119422,RMVar_hsa_circ_96945,RMVar_hsa_circ_64037,RMVar_hsa_circ_172153,RMVar_hsa_circ_172154,RMVar_hsa_circ_27808,RMVar_hsa_circ_27761,RMVar_hsa_circ_88272,RMVar_hsa_circ_36741,RMVar_hsa_circ_37856,RMVar_hsa_circ_172157,RMVar_hsa_circ_104238,RMVar_hsa_circ_72503,RMVar_hsa_circ_26927,RMVar_hsa_circ_172158,RMVar_hsa_circ_309897,RMVar_hsa_circ_339583,RMVar_hsa_circ_375907,RMVar_hsa_circ_172160,RMVar_hsa_circ_348159,RMVar_hsa_circ_289030,RMVar_hsa_circ_172161,RMVar_hsa_circ_172162,RMVar_hsa_circ_172163 44157 RMVar_ID_44157 Human_SNP_ID_577450819 A-to-I Human chr15 - 52381979 52381979 52381979 AGAATCACTTGAACCTGGGAGGCTGCAGTTGCAGTGAGCCGAGATCACTCCACTGCACTCTAGCC AGAATCACTTGAACCTGGGAGGCTGCAGTTGCCGTGAGCCGAGATCACTCCACTGCACTCTAGCC T G MYO5A Ensembl:ENSG00000197535 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1471498312 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97707,RMVar_hsa_circ_172150,RMVar_hsa_circ_119422,RMVar_hsa_circ_96945,RMVar_hsa_circ_64037,RMVar_hsa_circ_172153,RMVar_hsa_circ_172154,RMVar_hsa_circ_27808,RMVar_hsa_circ_27761,RMVar_hsa_circ_88272,RMVar_hsa_circ_36741,RMVar_hsa_circ_37856,RMVar_hsa_circ_172157,RMVar_hsa_circ_104238,RMVar_hsa_circ_72503,RMVar_hsa_circ_26927,RMVar_hsa_circ_172158,RMVar_hsa_circ_309897,RMVar_hsa_circ_339583,RMVar_hsa_circ_375907,RMVar_hsa_circ_172160,RMVar_hsa_circ_348159,RMVar_hsa_circ_289030,RMVar_hsa_circ_172161,RMVar_hsa_circ_172162,RMVar_hsa_circ_172163 44158 RMVar_ID_44158 Human_SNP_ID_577450982 A-to-I Human chr15 - 52382532 52382532 52382532 AGTTTCACTCTTCTTGCCCTGGCTGGAGTGCAATAACGCGATCTCGGCTTACCGCAACCTCTGCC AGTTTCACTCTTCTTGCCCTGGCTGGAGTGCAGTAACGCGATCTCGGCTTACCGCAACCTCTGCC T C MYO5A Ensembl:ENSG00000197535 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1333953652 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97707,RMVar_hsa_circ_172150,RMVar_hsa_circ_119422,RMVar_hsa_circ_96945,RMVar_hsa_circ_64037,RMVar_hsa_circ_172153,RMVar_hsa_circ_172154,RMVar_hsa_circ_27808,RMVar_hsa_circ_27761,RMVar_hsa_circ_88272,RMVar_hsa_circ_36741,RMVar_hsa_circ_37856,RMVar_hsa_circ_172157,RMVar_hsa_circ_104238,RMVar_hsa_circ_72503,RMVar_hsa_circ_26927,RMVar_hsa_circ_172158,RMVar_hsa_circ_309897,RMVar_hsa_circ_339583,RMVar_hsa_circ_375907,RMVar_hsa_circ_172160,RMVar_hsa_circ_348159,RMVar_hsa_circ_289030,RMVar_hsa_circ_172161,RMVar_hsa_circ_172162,RMVar_hsa_circ_172163 44159 RMVar_ID_44159 Human_SNP_ID_577483340 A-to-I Human chr15 - 52513309 52513309 52513309 CTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTATAGGCACATGGCACCACACCCTGCTAATTTTT CTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTGTAGGCACATGGCACCACACCCTGCTAATTTTT T C MYO5A Ensembl:ENSG00000197535 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1318165867 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114537,RMVar_hsa_circ_172168,RMVar_hsa_circ_172177 44160 RMVar_ID_44160 Human_SNP_ID_577494960 A-to-I Human chr15 - 52558939 52558939 52558939 TGTATGAGAGCTGGATGTGGTGGTGCATGCCTATAATCCCAGCACATTGGGAGGCTGAGGTGAGA TGTATGAGAGCTGGATGTGGTGGTGCATGCCTGTAATCCCAGCACATTGGGAGGCTGAGGTGAGA T C ARPP19 Ensembl:ENSG00000128989 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs751802199 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125363,RMVar_hsa_circ_172185,RMVar_hsa_circ_76522,RMVar_hsa_circ_172184 44161 RMVar_ID_44161 Human_SNP_ID_577496493 A-to-I Human chr15 - 52564406 52564404 52564406 AGGCTGAAGAATGTTTTTGTTATGTTTGAGACAGGGTCTTACTCTGTCGCCCAGGCTGGGGTGCA AGGCTGAAGAATGTTTTTGTTATGTTTGAGAC__GGTCTTACTCTGTCGCCCAGGCTGGGGTGCA CCT C ARPP19 Ensembl:ENSG00000128989 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1489392591 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_125363,RMVar_hsa_circ_172185,RMVar_hsa_circ_76522,RMVar_hsa_circ_172184 44162 RMVar_ID_44162 Human_SNP_ID_577496494 A-to-I Human chr15 - 52564406 52564406 52564406 AGGCTGAAGAATGTTTTTGTTATGTTTGAGACAGGGTCTTACTCTGTCGCCCAGGCTGGGGTGCA AGGCTGAAGAATGTTTTTGTTATGTTTGAGACGGGGTCTTACTCTGTCGCCCAGGCTGGGGTGCA T C ARPP19 Ensembl:ENSG00000128989 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1291787985 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125363,RMVar_hsa_circ_172185,RMVar_hsa_circ_76522,RMVar_hsa_circ_172184 44163 RMVar_ID_44163 Human_SNP_ID_577502923 A-to-I Human chr15 - 52589855 52589855 52589855 TGAACCCAGGAGGCAGAGGTTGCACTGAGCCAAGATCGTGTCACTGCACTCCAGTCTGGATGACA TGAACCCAGGAGGCAGAGGTTGCACTGAGCCAGGATCGTGTCACTGCACTCCAGTCTGGATGACA T C FAM214A Ensembl:ENSG00000047346 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1460771149 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58497,RMVar_hsa_circ_319013,RMVar_hsa_circ_360823,RMVar_hsa_circ_371644,RMVar_hsa_circ_330710,RMVar_hsa_circ_271149,RMVar_hsa_circ_172190,RMVar_hsa_circ_126861,RMVar_hsa_circ_172188,RMVar_hsa_circ_172189,RMVar_hsa_circ_172187,RMVar_hsa_circ_75506 44164 RMVar_ID_44164 Human_SNP_ID_577503670 A-to-I Human chr15 - 52592962 52592962 52592962 TTTTATGTTTTGTAGAGGCAGGGCCTCCCTATATTGCCCAGGCTGGTCTTGAACTCCTGGCCTCA TTTTATGTTTTGTAGAGGCAGGGCCTCCCTATGTTGCCCAGGCTGGTCTTGAACTCCTGGCCTCA T C FAM214A Ensembl:ENSG00000047346 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs183121819 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58497,RMVar_hsa_circ_319013,RMVar_hsa_circ_360823,RMVar_hsa_circ_371644,RMVar_hsa_circ_330710,RMVar_hsa_circ_271149,RMVar_hsa_circ_172190,RMVar_hsa_circ_126861,RMVar_hsa_circ_172188,RMVar_hsa_circ_172189,RMVar_hsa_circ_172187,RMVar_hsa_circ_75506 44165 RMVar_ID_44165 Human_SNP_ID_577514706 A-to-I Human chr15 - 52637148 52637148 52637148 GCCCATAGGACTTTGATGTTTAACAGCAAACAAAAATGATAAATACATGTAGCATTCACGAAGTC GCCCATAGGACTTTGATGTTTAACAGCAAACAGAAATGATAAATACATGTAGCATTCACGAAGTC T C FAM214A Ensembl:ENSG00000047346 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs571159381 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2243530 RMVar_hsa_circ_360823,RMVar_hsa_circ_53566,RMVar_hsa_circ_78068,RMVar_hsa_circ_361408,RMVar_hsa_circ_172191,RMVar_hsa_circ_359572,RMVar_hsa_circ_366463,RMVar_hsa_circ_365035 44166 RMVar_ID_44166 Human_SNP_ID_577516746 A-to-I Human chr15 - 52645234 52645234 52645234 GGGTTTCACCATGTTCGCCAGGCTGGCCTCGAACTCTTGACATCAAGTGATGTGCCTGCCTCGGC GGGTTTCACCATGTTCGCCAGGCTGGCCTCGAGCTCTTGACATCAAGTGATGTGCCTGCCTCGGC T C FAM214A Ensembl:ENSG00000047346 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs927277607 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_360823,RMVar_hsa_circ_53566,RMVar_hsa_circ_78068,RMVar_hsa_circ_361408,RMVar_hsa_circ_172191,RMVar_hsa_circ_359572,RMVar_hsa_circ_366463,RMVar_hsa_circ_365035 44167 RMVar_ID_44167 Human_SNP_ID_577921833 A-to-I Human chr15 + 54161198 54161198 54161198 ATGGCTCACTGCAGCTTCAATTTCTCATGCTCAAGTTATCCTCCGACCTCAGCCTCCCAAATAGC ATGGCTCACTGCAGCTTCAATTTCTCATGCTCTAGTTATCCTCCGACCTCAGCCTCCCAAATAGC A T UNC13C Ensembl:ENSG00000137766 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs904554146 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26641,RMVar_hsa_circ_6464,RMVar_hsa_circ_28280,RMVar_hsa_circ_279758 44168 RMVar_ID_44168 Human_SNP_ID_577982539 A-to-I Human chr15 + 54384409 54384409 54384409 TCAACATAGATTCCAGGAACATACACTGGGGAAAGCACACTCTCTTCATTAAATGATGCTGGGGA TCAACATAGATTCCAGGAACATACACTGGGGAGAGCACACTCTCTTCATTAAATGATGCTGGGGA A G UNC13C Ensembl:ENSG00000137766 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1431179452 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25589,RMVar_hsa_circ_343111,RMVar_hsa_circ_289542,RMVar_hsa_circ_27618,RMVar_hsa_circ_172217,RMVar_hsa_circ_81250,RMVar_hsa_circ_127777,RMVar_hsa_circ_172218,RMVar_hsa_circ_377163,RMVar_hsa_circ_172219,RMVar_hsa_circ_25660,RMVar_hsa_circ_330269,RMVar_hsa_circ_331575,RMVar_hsa_circ_51991,RMVar_hsa_circ_172227,RMVar_hsa_circ_172228 44169 RMVar_ID_44169 Human_SNP_ID_578005732 A-to-I Human chr15 + 54466164 54466163 54466164 AAAAGAATTGATCTCATGGAGGTGGAGAGTAGAATGGTGGTTACCAGAGGTTGCAAAGGTGGGGA AAAAGAATTGATCTCATGGAGGTGGAGAGTAG_ATGGTGGTTACCAGAGGTTGCAAAGGTGGGGA GA G UNC13C Ensembl:ENSG00000137766 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1438833141 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_25589,RMVar_hsa_circ_172217,RMVar_hsa_circ_81250,RMVar_hsa_circ_127777,RMVar_hsa_circ_172218,RMVar_hsa_circ_25660,RMVar_hsa_circ_51991,RMVar_hsa_circ_106024,RMVar_hsa_circ_265705,RMVar_hsa_circ_172230,RMVar_hsa_circ_21399 44170 RMVar_ID_44170 Human_SNP_ID_578005733 A-to-I Human chr15 + 54466164 54466164 54466164 AAAAGAATTGATCTCATGGAGGTGGAGAGTAGAATGGTGGTTACCAGAGGTTGCAAAGGTGGGGA AAAAGAATTGATCTCATGGAGGTGGAGAGTAGCATGGTGGTTACCAGAGGTTGCAAAGGTGGGGA A C UNC13C Ensembl:ENSG00000137766 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs573746542 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25589,RMVar_hsa_circ_172217,RMVar_hsa_circ_81250,RMVar_hsa_circ_127777,RMVar_hsa_circ_172218,RMVar_hsa_circ_25660,RMVar_hsa_circ_51991,RMVar_hsa_circ_106024,RMVar_hsa_circ_265705,RMVar_hsa_circ_172230,RMVar_hsa_circ_21399 44171 RMVar_ID_44171 Human_SNP_ID_578230840 A-to-I Human chr15 - 55287695 55287694 55287696 TTTACCAGGCTGGAGTGCAATGGCACGATCTCAGCTCACTGCAACCTCCGCCTCCCTGGTTCAAG TTTACCAGGCTGGAGTGCAATGGCACGATCT__GCTCACTGCAACCTCCGCCTCCCTGGTTCAAG CTG C RAB27A Ensembl:ENSG00000069974 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1359814755 Functional Loss DEL dbSNP153 32..33 33 - - - 44172 RMVar_ID_44172 Human_SNP_ID_578239868 A-to-I Human chr15 - 55318334 55318334 55318334 CCAGTACTTTGGGAGGCCAAGACGGGCGGATCAGGAGGTCAGAGGATCGAGACCATCCTGGCTAA CCAGTACTTTGGGAGGCCAAGACGGGCGGATCGGGAGGTCAGAGGATCGAGACCATCCTGGCTAA T C PIGBOS1,RAB27A Ensembl:ENSG00000225973,Ensembl:ENSG00000069974 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs954432990 Functional Loss SNV dbSNP153 33..33 33 - - - 44173 RMVar_ID_44173 Human_SNP_ID_578241529 A-to-I Human chr15 + 55324124 55324124 55324124 CCAGGCTGGACTCAAATGATCTGCCTGCCTCTACCTCCCAAAGTGTTGAGATTACAGGGGTGAGC CCAGGCTGGACTCAAATGATCTGCCTGCCTCTGCCTCCCAAAGTGTTGAGATTACAGGGGTGAGC A G PIGB Ensembl:ENSG00000069943 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs763106723 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123546,RMVar_hsa_circ_95535,RMVar_hsa_circ_172240,RMVar_hsa_circ_95236,RMVar_hsa_circ_172241,RMVar_hsa_circ_172242 44174 RMVar_ID_44174 Human_SNP_ID_578241530 A-to-I Human chr15 + 55324131 55324131 55324131 GGACTCAAATGATCTGCCTGCCTCTACCTCCCAAAGTGTTGAGATTACAGGGGTGAGCCACCAAG GGACTCAAATGATCTGCCTGCCTCTACCTCCCGAAGTGTTGAGATTACAGGGGTGAGCCACCAAG A G PIGB Ensembl:ENSG00000069943 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049714647 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123546,RMVar_hsa_circ_95535,RMVar_hsa_circ_172240,RMVar_hsa_circ_95236,RMVar_hsa_circ_172241,RMVar_hsa_circ_172242 44175 RMVar_ID_44175 Human_SNP_ID_578244448 A-to-I Human chr15 + 55336144 55336144 55336144 TATCATAAGTCAGGCAAGGCACAGTGGCTCACACCTGTAATCCCAGTGCCCTGGGAGACCAGGAG TATCATAAGTCAGGCAAGGCACAGTGGCTCACCCCTGTAATCCCAGTGCCCTGGGAGACCAGGAG A C PIGB Ensembl:ENSG00000069943 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs562619948 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_46711,RMVar_hsa_circ_123546,RMVar_hsa_circ_95535,RMVar_hsa_circ_172240,RMVar_hsa_circ_95236,RMVar_hsa_circ_172241,RMVar_hsa_circ_286884,RMVar_hsa_circ_365869,RMVar_hsa_circ_172242,RMVar_hsa_circ_172245,RMVar_hsa_circ_172246,RMVar_hsa_circ_294097,RMVar_hsa_circ_172247 44176 RMVar_ID_44176 Human_SNP_ID_578247211 A-to-I Human chr15 + 55347382 55347382 55347382 CCAGGAGGTGGAGGTTGCAGTGAGCCGGTATCATGCCACTTGCACTCCCGCCTGGGCGAAAGAGC CCAGGAGGTGGAGGTTGCAGTGAGCCGGTATCGTGCCACTTGCACTCCCGCCTGGGCGAAAGAGC A G PIGB Ensembl:ENSG00000069943 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1393527080 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_365869,RMVar_hsa_circ_85885,RMVar_hsa_circ_172248 44177 RMVar_ID_44177 Human_SNP_ID_578248686 A-to-I Human chr15 - 55352705 55352705 55352705 TCGCCCAGGTTGGAGTGCAATGGTATGACCTCAGCTCACTGCAACCTCCGCCTCCCGAGTAGCTA TCGCCCAGGTTGGAGTGCAATGGTATGACCTCTGCTCACTGCAACCTCCGCCTCCCGAGTAGCTA T A CCPG1 Ensembl:ENSG00000260916 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs951862135 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172251,RMVar_hsa_circ_172250 44178 RMVar_ID_44178 Human_SNP_ID_578249418 A-to-I Human chr15 + 55355399 55355398 55355399 GGAAGTCACATATATGTCTATGAACGGAAGTTAAAAGGGAAATTCAACATGAAGATGAAATTCTG GGAAGTCACATATATGTCTATGAACGGAAGTT_AAAGGGAAATTCAACATGAAGATGAAATTCTG TA T PIGB Ensembl:ENSG00000069943 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs746015165 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_459372 Human_miRNA_ID_543745,Human_miRNA_ID_578978 44179 RMVar_ID_44179 Human_SNP_ID_578249451 A-to-I Human chr15 + 55355525 55355525 55355525 GGTAAACACTGGGTAAGATTCATGGAACTTAGAAAAAAGCTGTATGAACTGCTTTACCAAATATC GGTAAACACTGGGTAAGATTCATGGAACTTAGGAAAAAGCTGTATGAACTGCTTTACCAAATATC A G PIGB Ensembl:ENSG00000069943 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs746244095 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1773778 44180 RMVar_ID_44180 Human_SNP_ID_578251538 A-to-I Human chr15 + 55363388 55363387 55363388 AAACAAACAAAACAAAAAAAAAACCCAAACCCAAACCAAACTACAAACTCTCTCTAGAGGTTAAT AAACAAACAAAACAAAAAAAAAACCCAAACCC_AACCAAACTACAAACTCTCTCTAGAGGTTAAT CA C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs796788289 Functional Loss DEL dbSNP153 33..33 33 - - - 44181 RMVar_ID_44181 Human_SNP_ID_578251539 A-to-I Human chr15 + 55363388 55363388 55363388 AAACAAACAAAACAAAAAAAAAACCCAAACCCAAACCAAACTACAAACTCTCTCTAGAGGTTAAT AAACAAACAAAACAAAAAAAAAACCCAAACCCGAACCAAACTACAAACTCTCTCTAGAGGTTAAT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1044329795 Functional Loss SNV dbSNP153 33..33 33 - - - 44182 RMVar_ID_44182 Human_SNP_ID_578253617 A-to-I Human chr15 - 55371001 55371001 55371001 TCTAGCAATTCTCCTACCTCAGCCTCCGGAGTAACTGGGATAACAGGCGCCCGCCACCATGCCTG TCTAGCAATTCTCCTACCTCAGCCTCCGGAGTGACTGGGATAACAGGCGCCCGCCACCATGCCTG T C CCPG1,DNAAF4-CCPG1 Ensembl:ENSG00000260916,Ensembl:ENSG00000261771 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1260581934 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_46712,RMVar_hsa_circ_172250,RMVar_hsa_circ_293636,RMVar_hsa_circ_343625,RMVar_hsa_circ_172253 44183 RMVar_ID_44183 Human_SNP_ID_578255262 A-to-I Human chr15 - 55376982 55376980 55376983 GTTCAGAAGACTTTAACATGGGCTCTTCCTCTAGCAGCCAGTATACTTTCTGTCAGCCAGAAACT GTTCAGAAGACTTTAACATGGGCTCTTCCTC___CAGCCAGTATACTTTCTGTCAGCCAGAAACT GCTA G CCPG1,DNAAF4-CCPG1 Ensembl:ENSG00000260916,Ensembl:ENSG00000261771 Protein coding,lincRNA CDS,exon GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1350097988 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_1511692,Human_RBP_ID_3490733,Human_RBP_ID_5096246,Human_RBP_ID_5569584,Human_RBP_ID_8800724,Human_RBP_ID_27810335 Human_Splice_Rec_1604937,Human_Splice_Rec_1604953,Human_Splice_Rec_1604967,Human_Splice_Rec_1604993,Human_Splice_Rec_1605005,Human_Splice_Rec_1605019,Human_Splice_Rec_1605031,Human_Splice_Rec_1605065 Human_miRNA_ID_2332508,Human_miRNA_ID_2332509,Human_miRNA_ID_2965594,Human_miRNA_ID_2965595,Human_miRNA_ID_3094929,Human_miRNA_ID_3094930,Human_miRNA_ID_3169200,Human_miRNA_ID_3206979,Human_miRNA_ID_3214820 RMVar_hsa_circ_172254,RMVar_hsa_circ_42300,RMVar_hsa_circ_46712,RMVar_hsa_circ_343625,RMVar_hsa_circ_273974,RMVar_hsa_circ_286940,RMVar_hsa_circ_305701,RMVar_hsa_circ_321649,RMVar_hsa_circ_288287,RMVar_hsa_circ_124616,RMVar_hsa_circ_172256,RMVar_hsa_circ_172258,RMVar_hsa_circ_172259,RMVar_hsa_circ_172257,RMVar_hsa_circ_172255 44184 RMVar_ID_44184 Human_SNP_ID_578271280 A-to-I Human chr15 - 55432780 55432780 55432780 ACAGCCAGATAATTTTTGTATTTTTTTTTAGTAGAGACGGGGTTTCGCCATGTTGGCCAGGCTGG ACAGCCAGATAATTTTTGTATTTTTTTTTAGTGGAGACGGGGTTTCGCCATGTTGGCCAGGCTGG T C DNAAF4,DNAAF4-CCPG1 Ensembl:ENSG00000256061,Ensembl:ENSG00000261771 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1233144373 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42300,RMVar_hsa_circ_124616,RMVar_hsa_circ_172259,RMVar_hsa_circ_172262,RMVar_hsa_circ_68501,RMVar_hsa_circ_300121,RMVar_hsa_circ_325680,RMVar_hsa_circ_287013,RMVar_hsa_circ_172263,RMVar_hsa_circ_172261 44185 RMVar_ID_44185 Human_SNP_ID_578271282 A-to-I Human chr15 - 55432783 55432783 55432783 ACCACAGCCAGATAATTTTTGTATTTTTTTTTAGTAGAGACGGGGTTTCGCCATGTTGGCCAGGC ACCACAGCCAGATAATTTTTGTATTTTTTTTTTGTAGAGACGGGGTTTCGCCATGTTGGCCAGGC T A DNAAF4,DNAAF4-CCPG1 Ensembl:ENSG00000256061,Ensembl:ENSG00000261771 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924034511 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42300,RMVar_hsa_circ_124616,RMVar_hsa_circ_172259,RMVar_hsa_circ_172262,RMVar_hsa_circ_68501,RMVar_hsa_circ_300121,RMVar_hsa_circ_325680,RMVar_hsa_circ_287013,RMVar_hsa_circ_172263,RMVar_hsa_circ_172261 44186 RMVar_ID_44186 Human_SNP_ID_578281081 A-to-I Human chr15 - 55463088 55463077 55463088 CTCACTGCAACCTCTGCCTCCCAAATTCAAGCAGTTCTCCTGCCTCAACCTCCCCAGTATCTGGG CTCACTGCAACCTCTGCCTCCCAAATTCAAGC___________CTCAACCTCCCCAGTATCTGGG GGCAGGAGAACT G DNAAF4,DNAAF4-CCPG1 Ensembl:ENSG00000256061,Ensembl:ENSG00000261771 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs766967891 Functional Loss DEL dbSNP153 33..43 33 - - - RMVar_hsa_circ_124616,RMVar_hsa_circ_172259,RMVar_hsa_circ_172262,RMVar_hsa_circ_68501,RMVar_hsa_circ_300121,RMVar_hsa_circ_13200,RMVar_hsa_circ_172261,RMVar_hsa_circ_326956,RMVar_hsa_circ_172266,RMVar_hsa_circ_72114 44187 RMVar_ID_44187 Human_SNP_ID_578383368 A-to-I Human chr15 - 55834726 55834726 55834726 GTTTTTTGTTGTTGTTCTTGTTGTTTTGAGACAGGATCTCACTTTTTGCCGAGGCTGGAATACCT GTTTTTTGTTGTTGTTCTTGTTGTTTTGAGACGGGATCTCACTTTTTGCCGAGGCTGGAATACCT T C NEDD4 Ensembl:ENSG00000069869 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973402756 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3239,RMVar_hsa_circ_79392,RMVar_hsa_circ_172275,RMVar_hsa_circ_67806,RMVar_hsa_circ_51192,RMVar_hsa_circ_55562 44188 RMVar_ID_44188 Human_SNP_ID_578383858 A-to-I Human chr15 - 55836664 55836664 55836664 AAAATTAGCCGGACGTGGTGGCGTGCACGTGCAGTCCCAGCTACTCGGGAGGCTGAGGCAGGGGA AAAATTAGCCGGACGTGGTGGCGTGCACGTGCGGTCCCAGCTACTCGGGAGGCTGAGGCAGGGGA T C NEDD4 Ensembl:ENSG00000069869 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1190049773 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3239,RMVar_hsa_circ_79392,RMVar_hsa_circ_172275,RMVar_hsa_circ_67806,RMVar_hsa_circ_51192,RMVar_hsa_circ_55562 44189 RMVar_ID_44189 Human_SNP_ID_578383943 A-to-I Human chr15 - 55836925 55836925 55836925 GCTGGGCATGGTGGCTGACGCCTAAAATCCCAACACTTGAGGAGGCTGAGGCGGGAGGATTGCTT GCTGGGCATGGTGGCTGACGCCTAAAATCCCAGCACTTGAGGAGGCTGAGGCGGGAGGATTGCTT T C NEDD4 Ensembl:ENSG00000069869 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1383735614 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3239,RMVar_hsa_circ_79392,RMVar_hsa_circ_172275,RMVar_hsa_circ_67806,RMVar_hsa_circ_51192,RMVar_hsa_circ_55562 44190 RMVar_ID_44190 Human_SNP_ID_578389811 A-to-I Human chr15 - 55859585 55859585 55859585 TCAGGCGATTCTCATGCCTCAGCCTCCTGAATAGCTGAGATTACAGGCGCACACCACCACGCCCA TCAGGCGATTCTCATGCCTCAGCCTCCTGAATGGCTGAGATTACAGGCGCACACCACCACGCCCA T C NEDD4 Ensembl:ENSG00000069869 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs529223615 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172282,RMVar_hsa_circ_3239,RMVar_hsa_circ_54003,RMVar_hsa_circ_52006,RMVar_hsa_circ_83413,RMVar_hsa_circ_36043,RMVar_hsa_circ_27292,RMVar_hsa_circ_268063,RMVar_hsa_circ_70143,RMVar_hsa_circ_172278,RMVar_hsa_circ_41261,RMVar_hsa_circ_116185,RMVar_hsa_circ_339908,RMVar_hsa_circ_50179,RMVar_hsa_circ_117735,RMVar_hsa_circ_62520,RMVar_hsa_circ_172283,RMVar_hsa_circ_172281 44191 RMVar_ID_44191 Human_SNP_ID_578400418 A-to-I Human chr15 - 55904499 55904499 55904499 CAGGACTTTGAGACAGGCTTGGCCAGCATGGTAAAACCTCGTCTCTACTGAAAACAGAAAAATTA CAGGACTTTGAGACAGGCTTGGCCAGCATGGTGAAACCTCGTCTCTACTGAAAACAGAAAAATTA T C NEDD4 Ensembl:ENSG00000069869 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1465184685 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268063 44192 RMVar_ID_44192 Human_SNP_ID_578421653 A-to-I Human chr15 - 55983683 55983683 55983683 TTGTTTGAATCGGGAGGTGGGGGTTGCAGTGAACCGAGACTGCGCCACTGCACTCCAGTCTGGGC TTGTTTGAATCGGGAGGTGGGGGTTGCAGTGAGCCGAGACTGCGCCACTGCACTCCAGTCTGGGC T C NEDD4 Ensembl:ENSG00000069869 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1200372815 Functional Loss SNV dbSNP153 33..33 33 - - - 44193 RMVar_ID_44193 Human_SNP_ID_578439450 A-to-I Human chr15 + 56053483 56053483 56053483 GTGGCACAGCATGAGGTGAGCTGCGAGTGAGCATTACCACCTGAGCTCTGTCTCCTGTCAGATCA GTGGCACAGCATGAGGTGAGCTGCGAGTGAGCGTTACCACCTGAGCTCTGTCTCCTGTCAGATCA A G 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 RNACentral:URS0000D5B96D,RNACentral:URS0000D5C656,RNACentral:URS0000D5C4BE,RNACentral:URS0000D5AAA5,RNACentral:URS0000D56E7A,RNACentral:URS0000D57BB3,RNACentral:URS0000D5765A lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1385864925 Functional Loss SNV dbSNP153 33..33 33 - - - 44194 RMVar_ID_44194 Human_SNP_ID_578439451 A-to-I Human chr15 + 56053483 56053483 56053483 GTGGCACAGCATGAGGTGAGCTGCGAGTGAGCATTACCACCTGAGCTCTGTCTCCTGTCAGATCA GTGGCACAGCATGAGGTGAGCTGCGAGTGAGCTTTACCACCTGAGCTCTGTCTCCTGTCAGATCA A T 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 RNACentral:URS0000D5B96D,RNACentral:URS0000D5C656,RNACentral:URS0000D5C4BE,RNACentral:URS0000D5AAA5,RNACentral:URS0000D56E7A,RNACentral:URS0000D57BB3,RNACentral:URS0000D5765A lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1385864925 Functional Loss SNV dbSNP153 33..33 33 - - - 44195 RMVar_ID_44195 Human_SNP_ID_578441423 A-to-I Human chr15 + 56060781 56060781 56060781 GCGATCTCGGATCACTGCAAGCTCCGCCTCCTAGATTCATGCCATTCTCCTGACTAAGCCTCCCT GCGATCTCGGATCACTGCAAGCTCCGCCTCCTGGATTCATGCCATTCTCCTGACTAAGCCTCCCT A G 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 RNACentral:URS0000D5B96D,RNACentral:URS0000D5C656,RNACentral:URS0000D5C4BE,RNACentral:URS0000D5AAA5,RNACentral:URS0000D56E7A,RNACentral:URS0000D57BB3,RNACentral:URS0000D5765A lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1402338531 Functional Loss SNV dbSNP153 33..33 33 - - - 44196 RMVar_ID_44196 Human_SNP_ID_578464483 A-to-I Human chr15 - 56141322 56141322 56141322 AACTCTTGTCACCTAGGCTGGAGTGCAATGGCACGATCACAGCTCACTGCAGCTTTAACTCCCAC AACTCTTGTCACCTAGGCTGGAGTGCAATGGCCCGATCACAGCTCACTGCAGCTTTAACTCCCAC T G RFX7 Ensembl:ENSG00000181827 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1407534941 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22929364 RMVar_hsa_circ_102861,RMVar_hsa_circ_121844,RMVar_hsa_circ_123578,RMVar_hsa_circ_172289,RMVar_hsa_circ_106509,RMVar_hsa_circ_172290,RMVar_hsa_circ_172288,RMVar_hsa_circ_95291,RMVar_hsa_circ_60355,RMVar_hsa_circ_172291,RMVar_hsa_circ_172293,RMVar_hsa_circ_119931,RMVar_hsa_circ_172294 44197 RMVar_ID_44197 Human_SNP_ID_578474491 A-to-I Human chr15 - 56180713 56180713 56180713 TTAGTAGATATGGGGTTTTACCGTGTTGCCCAAGCTGGTCTCGAACTCCTGAGCCAAGGCAATCC TTAGTAGATATGGGGTTTTACCGTGTTGCCCATGCTGGTCTCGAACTCCTGAGCCAAGGCAATCC T A RFX7 Ensembl:ENSG00000181827 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569568277 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12534920 RMVar_hsa_circ_102861,RMVar_hsa_circ_121844,RMVar_hsa_circ_172290,RMVar_hsa_circ_95291,RMVar_hsa_circ_172291,RMVar_hsa_circ_172293,RMVar_hsa_circ_119931,RMVar_hsa_circ_95934,RMVar_hsa_circ_172294,RMVar_hsa_circ_172297,RMVar_hsa_circ_172298,RMVar_hsa_circ_117711 44198 RMVar_ID_44198 Human_SNP_ID_578542741 A-to-I Human chr15 + 56442788 56442788 56442788 GGTGAGGATCAATAAACTACCTATCGAGTACTATGCTCATTACTTGGGTGACAAAATAATGTTAC GGTGAGGATCAATAAACTACCTATCGAGTACTGTGCTCATTACTTGGGTGACAAAATAATGTTAC A G TEX9 Ensembl:ENSG00000151575 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1230137957 Functional Loss SNV dbSNP153 33..33 33 - - - 44199 RMVar_ID_44199 Human_SNP_ID_578595842 A-to-I Human chr15 - 56645826 56645826 56645826 TTTGTATGGATTGGCTGGGCACGGTGGCTCATACCTGTAATCCCAGCACTTTGGAAGGCCGAGGC TTTGTATGGATTGGCTGGGCACGGTGGCTCATGCCTGTAATCCCAGCACTTTGGAAGGCCGAGGC T C ZNF280D Ensembl:ENSG00000137871 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs374370836 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172319,RMVar_hsa_circ_42560,RMVar_hsa_circ_319561,RMVar_hsa_circ_315222,RMVar_hsa_circ_172321 44200 RMVar_ID_44200 Human_SNP_ID_578660478 A-to-I Human chr15 - 56905842 56905842 56905842 TTGAGACAGAGTCTCACTCTTTTGCCCAAATTAGAGTGCAATGACACGATCTCGACTCACTGCAA TTGAGACAGAGTCTCACTCTTTTGCCCAAATTCGAGTGCAATGACACGATCTCGACTCACTGCAA T G AC090517.4,AC090517.5 Ensembl:ENSG00000285253,Ensembl:ENSG00000285331 Protein coding,lincRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968973272 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1606172 RMVar_hsa_circ_172344 44201 RMVar_ID_44201 Human_SNP_ID_578661270 A-to-I Human chr15 - 56909312 56909311 56909312 TCACTCACGCTAGAGTGCAGTGGCCCAATCTCAGCTCACTGCAACCTCCCCTCCTGGGTTCAAGA TCACTCACGCTAGAGTGCAGTGGCCCAATCTC_GCTCACTGCAACCTCCCCTCCTGGGTTCAAGA CT C AC090517.4,AC090517.5 Ensembl:ENSG00000285253,Ensembl:ENSG00000285331 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs200618323 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_172344 44202 RMVar_ID_44202 Human_SNP_ID_578662030 A-to-I Human chr15 - 56912020 56912020 56912020 GCAAGACCCCATCTCTACAAAAAATTTTTAAAATTTAGCTGGATATGGTAGCATGCACCTGTGGT GCAAGACCCCATCTCTACAAAAAATTTTTAAACTTTAGCTGGATATGGTAGCATGCACCTGTGGT T G AC090517.4,AC090517.5 Ensembl:ENSG00000285253,Ensembl:ENSG00000285331 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388013256 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172344 44203 RMVar_ID_44203 Human_SNP_ID_578678527 A-to-I Human chr15 + 56969577 56969577 56969577 TTTTTTTTTTTGAGACGAGATTTCATTCTGTCACCCGGACTGGAGGGCAGTGATGTGATCTTGGC TTTTTTTTTTTGAGACGAGATTTCATTCTGTCGCCCGGACTGGAGGGCAGTGATGTGATCTTGGC A G TCF12 Ensembl:ENSG00000140262 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1047617698 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12536681,Human_RBP_ID_23656953 RMVar_hsa_circ_50292,RMVar_hsa_circ_315004,RMVar_hsa_circ_342551,RMVar_hsa_circ_355202,RMVar_hsa_circ_344342,RMVar_hsa_circ_296460,RMVar_hsa_circ_25427,RMVar_hsa_circ_122225,RMVar_hsa_circ_172355,RMVar_hsa_circ_172356,RMVar_hsa_circ_172357 44204 RMVar_ID_44204 Human_SNP_ID_578680736 A-to-I Human chr15 + 56977569 56977567 56977569 TCGATATTCTGTGTGTGTGTGTGTGTGTATGTATGTGTGGAGAGAGAGAGACACACACACACAGA TCGATATTCTGTGTGTGTGTGTGTGTGTATG__TGTGTGGAGAGAGAGAGACACACACACACAGA GTA G TCF12 Ensembl:ENSG00000140262 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1266764824 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_12536752,Human_RBP_ID_23656970 RMVar_hsa_circ_50292,RMVar_hsa_circ_315004,RMVar_hsa_circ_342551,RMVar_hsa_circ_355202,RMVar_hsa_circ_344342,RMVar_hsa_circ_296460,RMVar_hsa_circ_25427,RMVar_hsa_circ_122225,RMVar_hsa_circ_172355,RMVar_hsa_circ_172356,RMVar_hsa_circ_172357 44205 RMVar_ID_44205 Human_SNP_ID_578680737 A-to-I Human chr15 + 56977569 56977569 56977569 TCGATATTCTGTGTGTGTGTGTGTGTGTATGTATGTGTGGAGAGAGAGAGACACACACACACAGA TCGATATTCTGTGTGTGTGTGTGTGTGTATGTGTGTGTGGAGAGAGAGAGACACACACACACAGA A G TCF12 Ensembl:ENSG00000140262 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs192910646 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12536752,Human_RBP_ID_23656970 RMVar_hsa_circ_50292,RMVar_hsa_circ_315004,RMVar_hsa_circ_342551,RMVar_hsa_circ_355202,RMVar_hsa_circ_344342,RMVar_hsa_circ_296460,RMVar_hsa_circ_25427,RMVar_hsa_circ_122225,RMVar_hsa_circ_172355,RMVar_hsa_circ_172356,RMVar_hsa_circ_172357 44206 RMVar_ID_44206 Human_SNP_ID_578688605 A-to-I Human chr15 + 57006805 57006805 57006805 GAGTGTGGTGGCATGCGTCTGTGGTCCCAGCTACTTGGGAGGCTGAGGTGGGAGGATTGCTTGAG GAGTGTGGTGGCATGCGTCTGTGGTCCCAGCTCCTTGGGAGGCTGAGGTGGGAGGATTGCTTGAG A C TCF12 Ensembl:ENSG00000140262 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1176661453 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50292,RMVar_hsa_circ_315004,RMVar_hsa_circ_342551,RMVar_hsa_circ_355202,RMVar_hsa_circ_344342,RMVar_hsa_circ_296460,RMVar_hsa_circ_25427,RMVar_hsa_circ_122225,RMVar_hsa_circ_172355,RMVar_hsa_circ_172356,RMVar_hsa_circ_172357 44207 RMVar_ID_44207 Human_SNP_ID_578688606 A-to-I Human chr15 + 57006805 57006805 57006805 GAGTGTGGTGGCATGCGTCTGTGGTCCCAGCTACTTGGGAGGCTGAGGTGGGAGGATTGCTTGAG GAGTGTGGTGGCATGCGTCTGTGGTCCCAGCTGCTTGGGAGGCTGAGGTGGGAGGATTGCTTGAG A G TCF12 Ensembl:ENSG00000140262 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1176661453 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50292,RMVar_hsa_circ_315004,RMVar_hsa_circ_342551,RMVar_hsa_circ_355202,RMVar_hsa_circ_344342,RMVar_hsa_circ_296460,RMVar_hsa_circ_25427,RMVar_hsa_circ_122225,RMVar_hsa_circ_172355,RMVar_hsa_circ_172356,RMVar_hsa_circ_172357 44208 RMVar_ID_44208 Human_SNP_ID_578696470 A-to-I Human chr15 + 57035450 57035450 57035450 CATGCCTGGCTAATTTTTTAAAATTTTTTTGTAGAGACGGGATCTCACTATGTTGTGTAGGCTGA CATGCCTGGCTAATTTTTTAAAATTTTTTTGTGGAGACGGGATCTCACTATGTTGTGTAGGCTGA A G TCF12 Ensembl:ENSG00000140262 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs546804283 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50292,RMVar_hsa_circ_315004,RMVar_hsa_circ_342551,RMVar_hsa_circ_355202,RMVar_hsa_circ_344342,RMVar_hsa_circ_296460,RMVar_hsa_circ_25427,RMVar_hsa_circ_122225,RMVar_hsa_circ_172355,RMVar_hsa_circ_172356,RMVar_hsa_circ_172357 44209 RMVar_ID_44209 Human_SNP_ID_578712754 A-to-I Human chr15 + 57094122 57094122 57094122 GTTGACCAGACTGGTTTTGAGCTCCTGGCCTCAAGTGATCCTTCTGCCCCAGCCTCCCAAAATGT GTTGACCAGACTGGTTTTGAGCTCCTGGCCTCGAGTGATCCTTCTGCCCCAGCCTCCCAAAATGT A G TCF12 Ensembl:ENSG00000140262 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1255870696 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1210,RMVar_hsa_circ_50292,RMVar_hsa_circ_315004,RMVar_hsa_circ_342551,RMVar_hsa_circ_355202,RMVar_hsa_circ_344342,RMVar_hsa_circ_25427,RMVar_hsa_circ_122225,RMVar_hsa_circ_172356,RMVar_hsa_circ_172357,RMVar_hsa_circ_346054,RMVar_hsa_circ_363770,RMVar_hsa_circ_172360,RMVar_hsa_circ_16176,RMVar_hsa_circ_60015,RMVar_hsa_circ_92544,RMVar_hsa_circ_322600,RMVar_hsa_circ_172361 44210 RMVar_ID_44210 Human_SNP_ID_578715822 A-to-I Human chr15 + 57105071 57105071 57105071 AATTTTTGTACTTTTAGTAGAGATGGCGTTTCACCATGTTGGCCAGGCTGGCTTTGAACTCCTGA AATTTTTGTACTTTTAGTAGAGATGGCGTTTCGCCATGTTGGCCAGGCTGGCTTTGAACTCCTGA A G TCF12 Ensembl:ENSG00000140262 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs914678175 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1210,RMVar_hsa_circ_50292,RMVar_hsa_circ_315004,RMVar_hsa_circ_342551,RMVar_hsa_circ_355202,RMVar_hsa_circ_344342,RMVar_hsa_circ_25427,RMVar_hsa_circ_122225,RMVar_hsa_circ_172356,RMVar_hsa_circ_172357,RMVar_hsa_circ_346054,RMVar_hsa_circ_363770,RMVar_hsa_circ_16176,RMVar_hsa_circ_60015,RMVar_hsa_circ_322600,RMVar_hsa_circ_172361 44211 RMVar_ID_44211 Human_SNP_ID_578715909 A-to-I Human chr15 + 57105442 57105442 57105442 GGTGGTGGTGGTGTTTTTTTAGACGGAGTCTCATTGTGTCACCTAGGCTAGACTGCAGTGGTGTG GGTGGTGGTGGTGTTTTTTTAGACGGAGTCTCGTTGTGTCACCTAGGCTAGACTGCAGTGGTGTG A G TCF12 Ensembl:ENSG00000140262 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs867709952 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12537523 RMVar_hsa_circ_1210,RMVar_hsa_circ_50292,RMVar_hsa_circ_315004,RMVar_hsa_circ_342551,RMVar_hsa_circ_355202,RMVar_hsa_circ_344342,RMVar_hsa_circ_25427,RMVar_hsa_circ_122225,RMVar_hsa_circ_172356,RMVar_hsa_circ_172357,RMVar_hsa_circ_346054,RMVar_hsa_circ_363770,RMVar_hsa_circ_16176,RMVar_hsa_circ_60015,RMVar_hsa_circ_322600,RMVar_hsa_circ_172361 44212 RMVar_ID_44212 Human_SNP_ID_578742617 A-to-I Human chr15 + 57202682 57202682 57202682 TGGTCTCGATCTCCCGACCTCCTGATCCACCTACCTCAGCCTCCCGAAGTGCTGGGATTACAGGT TGGTCTCGATCTCCCGACCTCCTGATCCACCTGCCTCAGCCTCCCGAAGTGCTGGGATTACAGGT A G TCF12 Ensembl:ENSG00000140262 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1465641813 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1210,RMVar_hsa_circ_50292,RMVar_hsa_circ_342551,RMVar_hsa_circ_355202,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_343935,RMVar_hsa_circ_19302,RMVar_hsa_circ_62833,RMVar_hsa_circ_117263,RMVar_hsa_circ_172365,RMVar_hsa_circ_172364 44213 RMVar_ID_44213 Human_SNP_ID_578745346 A-to-I Human chr15 + 57212332 57212331 57212332 TCTAGAGACGGTCTCTCTCTGTCACCCTCGCTAGAGTACAGTGGCACAATCATAGCTCACTGCAG TCTAGAGACGGTCTCTCTCTGTCACCCTCGCT_GAGTACAGTGGCACAATCATAGCTCACTGCAG TA T TCF12 Ensembl:ENSG00000140262 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1321211292 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_1210,RMVar_hsa_circ_50292,RMVar_hsa_circ_342551,RMVar_hsa_circ_355202,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_343935,RMVar_hsa_circ_19302,RMVar_hsa_circ_62833,RMVar_hsa_circ_117263,RMVar_hsa_circ_172365,RMVar_hsa_circ_172364 44214 RMVar_ID_44214 Human_SNP_ID_578754252 A-to-I Human chr15 + 57244018 57244018 57244018 CTTCCACCTCAGCCTCCTGAGTAACTGGGAATACAGGTGTATGCCACCGTGCCAAGCTAATTTTT CTTCCACCTCAGCCTCCTGAGTAACTGGGAATCCAGGTGTATGCCACCGTGCCAAGCTAATTTTT A C TCF12 Ensembl:ENSG00000140262 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1292192687 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1210,RMVar_hsa_circ_342551,RMVar_hsa_circ_25427,RMVar_hsa_circ_60015,RMVar_hsa_circ_366681,RMVar_hsa_circ_19302,RMVar_hsa_circ_62833,RMVar_hsa_circ_111968,RMVar_hsa_circ_290673,RMVar_hsa_circ_335020,RMVar_hsa_circ_68985,RMVar_hsa_circ_81714,RMVar_hsa_circ_58488,RMVar_hsa_circ_172366,RMVar_hsa_circ_172368,RMVar_hsa_circ_172369,RMVar_hsa_circ_172367,RMVar_hsa_circ_350936,RMVar_hsa_circ_47522,RMVar_hsa_circ_359055,RMVar_hsa_circ_333565,RMVar_hsa_circ_303949,RMVar_hsa_circ_338431,RMVar_hsa_circ_368248,RMVar_hsa_circ_22493 44215 RMVar_ID_44215 Human_SNP_ID_578767372 A-to-I Human chr15 + 57291686 57291686 57291686 AGCTGGGAGCATAAGAGTGCACCCCTATGCCTAGCTAATTTTTTTTATTTTTTGTAGAGTTGGAA AGCTGGGAGCATAAGAGTGCACCCCTATGCCTGGCTAATTTTTTTTATTTTTTGTAGAGTTGGAA A G TCF12 Ensembl:ENSG00000140262 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1381586691 Functional Loss SNV dbSNP153 33..33 33 - - - 44216 RMVar_ID_44216 Human_SNP_ID_578955196 A-to-I Human chr15 - 57954605 57954605 57954605 ACCAGAATGAAAATGCCAGGAGCTGGTACACTACAGATGTAGTAAGAACCTGGGATATTCCTGAC ACCAGAATGAAAATGCCAGGAGCTGGTACACTCCAGATGTAGTAAGAACCTGGGATATTCCTGAC T G ALDH1A2 Ensembl:ENSG00000128918 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1277371024 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8182880,Human_RBP_ID_17250386,Human_RBP_ID_17870132,Human_RBP_ID_18280371 RMVar_hsa_circ_103855,RMVar_hsa_circ_113865,RMVar_hsa_circ_172391,RMVar_hsa_circ_172392 44217 RMVar_ID_44217 Human_SNP_ID_579140584 A-to-I Human chr15 - 58604909 58604905 58604909 CTAGCAAGACCTGTGTGTGCAAATAAATAAATAAATGAATTCGCAGGGTGTGGCGGCATGTACCT CTAGCAAGACCTGTGTGTGCAAATAAATAAAT____GAATTCGCAGGGTGTGGCGGCATGTACCT CATTT C ADAM10 Ensembl:ENSG00000137845 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1490337443 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_31737 44218 RMVar_ID_44218 Human_SNP_ID_579140586 A-to-I Human chr15 - 58604909 58604909 58604909 CTAGCAAGACCTGTGTGTGCAAATAAATAAATAAATGAATTCGCAGGGTGTGGCGGCATGTACCT CTAGCAAGACCTGTGTGTGCAAATAAATAAATGAATGAATTCGCAGGGTGTGGCGGCATGTACCT T C ADAM10 Ensembl:ENSG00000137845 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1196295902 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_31737 44219 RMVar_ID_44219 Human_SNP_ID_579160855 A-to-I Human chr15 - 58679742 58679742 58679742 CACCAGGCCCAGCTAATGTTTTCTGTGTTTTTAGTAGAGACAGGGTTTCGCTATGTTAGCTAGGC CACCAGGCCCAGCTAATGTTTTCTGTGTTTTTCGTAGAGACAGGGTTTCGCTATGTTAGCTAGGC T G ADAM10 Ensembl:ENSG00000137845 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1473995294 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50343,RMVar_hsa_circ_72084,RMVar_hsa_circ_378549,RMVar_hsa_circ_10480,RMVar_hsa_circ_67497,RMVar_hsa_circ_321881,RMVar_hsa_circ_329001,RMVar_hsa_circ_172411,RMVar_hsa_circ_54401,RMVar_hsa_circ_300496,RMVar_hsa_circ_172414,RMVar_hsa_circ_172415,RMVar_hsa_circ_375317,RMVar_hsa_circ_366545,RMVar_hsa_circ_377396,RMVar_hsa_circ_341345,RMVar_hsa_circ_368881 44220 RMVar_ID_44220 Human_SNP_ID_579173117 A-to-I Human chr15 - 58721702 58721702 58721702 TTTTAATTTTTTGTAGAGACAGGGGCCTTTCTATGTTGCCTAGGCTGGTCTTGAACTCCTGGACT TTTTAATTTTTTGTAGAGACAGGGGCCTTTCTGTGTTGCCTAGGCTGGTCTTGAACTCCTGGACT T C ADAM10 Ensembl:ENSG00000137845 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1171033845 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116696,RMVar_hsa_circ_172416 44221 RMVar_ID_44221 Human_SNP_ID_579197674 A-to-I Human chr15 + 58806143 58806143 58806143 TTGTACAGGCTGGAGTGTAGTGGCATGATCTCAGCTCAGTACAACTTCCGCCTTTCAGGTTCAAG TTGTACAGGCTGGAGTGTAGTGGCATGATCTCGGCTCAGTACAACTTCCGCCTTTCAGGTTCAAG A G MINDY2 Ensembl:ENSG00000128923 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1276734984 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122751,RMVar_hsa_circ_172419,RMVar_hsa_circ_92778,RMVar_hsa_circ_172417,RMVar_hsa_circ_300133,RMVar_hsa_circ_172420,RMVar_hsa_circ_339095,RMVar_hsa_circ_369294,RMVar_hsa_circ_172421 44222 RMVar_ID_44222 Human_SNP_ID_579199841 A-to-I Human chr15 + 58814031 58814031 58814031 ACAATCTTTGCTCAGTGCAGCCTCCTGCTCCCAGGTTCAAGTGATGCTCCTGCCTCGACCTCCCG ACAATCTTTGCTCAGTGCAGCCTCCTGCTCCCGGGTTCAAGTGATGCTCCTGCCTCGACCTCCCG A G MINDY2 Ensembl:ENSG00000128923 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1295419324 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172419,RMVar_hsa_circ_300133,RMVar_hsa_circ_20413,RMVar_hsa_circ_330984,RMVar_hsa_circ_339095,RMVar_hsa_circ_310129,RMVar_hsa_circ_172422,RMVar_hsa_circ_172423 44223 RMVar_ID_44223 Human_SNP_ID_579199994 A-to-I Human chr15 + 58814581 58814581 58814581 TTTAATTTTTTGTAGAAATGAGATCTCGCCATATTGCTCAGGCTGGTCTCGAACTCCTGGGCTCA TTTAATTTTTTGTAGAAATGAGATCTCGCCATGTTGCTCAGGCTGGTCTCGAACTCCTGGGCTCA A G MINDY2 Ensembl:ENSG00000128923 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1192843173 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172419,RMVar_hsa_circ_300133,RMVar_hsa_circ_20413,RMVar_hsa_circ_330984,RMVar_hsa_circ_339095,RMVar_hsa_circ_310129,RMVar_hsa_circ_172422,RMVar_hsa_circ_172423 44224 RMVar_ID_44224 Human_SNP_ID_579201282 A-to-I Human chr15 + 58819411 58819411 58819411 TCGAGGCTGCAGTGGGCTGTGATCACGCCACTACATTCCAGCAAGAGTGACACAGTGAGACCCAG TCGAGGCTGCAGTGGGCTGTGATCACGCCACTGCATTCCAGCAAGAGTGACACAGTGAGACCCAG A G MINDY2 Ensembl:ENSG00000128923 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1048737805 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172419,RMVar_hsa_circ_300133,RMVar_hsa_circ_20413,RMVar_hsa_circ_330984,RMVar_hsa_circ_339095,RMVar_hsa_circ_310129,RMVar_hsa_circ_172422,RMVar_hsa_circ_172423 44225 RMVar_ID_44225 Human_SNP_ID_579201283 A-to-I Human chr15 + 58819411 58819411 58819411 TCGAGGCTGCAGTGGGCTGTGATCACGCCACTACATTCCAGCAAGAGTGACACAGTGAGACCCAG TCGAGGCTGCAGTGGGCTGTGATCACGCCACTTCATTCCAGCAAGAGTGACACAGTGAGACCCAG A T MINDY2 Ensembl:ENSG00000128923 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1048737805 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172419,RMVar_hsa_circ_300133,RMVar_hsa_circ_20413,RMVar_hsa_circ_330984,RMVar_hsa_circ_339095,RMVar_hsa_circ_310129,RMVar_hsa_circ_172422,RMVar_hsa_circ_172423 44226 RMVar_ID_44226 Human_SNP_ID_579218699 A-to-I Human chr15 - 58881320 58881306 58881320 AGGTTTCACTTTGTTGGCCAGGCTGGTCTCAAACTCCTGTTCCTCAGGTGATCCTCCAGCTTCAG AGGTTTCACTTTGTTGGCCAGGCTGGTCTCAA______________GGTGATCCTCCAGCTTCAG CTGAGGAACAGGAGT C SLTM Ensembl:ENSG00000137776 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1249107809 Functional Loss DEL dbSNP153 33..46 33 - - - 44227 RMVar_ID_44227 Human_SNP_ID_579218723 A-to-I Human chr15 - 58881403 58881403 58881403 CCTTCCTTGGCCTCCCAAGTAACTGGGACAACAGCGTGTGCCACCATGTTCAGCTGATTTTTTTG CCTTCCTTGGCCTCCCAAGTAACTGGGACAACCGCGTGTGCCACCATGTTCAGCTGATTTTTTTG T G SLTM Ensembl:ENSG00000137776 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1234400652 Functional Loss SNV dbSNP153 33..33 33 - - - 44228 RMVar_ID_44228 Human_SNP_ID_579218823 A-to-I Human chr15 - 58881843 58881843 58881843 CCTGTAATCCCAGTACTTTGGGAGGCCAAGGTAGGTAGATCACTTGAACTGAGGAGTTTGAGACC CCTGTAATCCCAGTACTTTGGGAGGCCAAGGTGGGTAGATCACTTGAACTGAGGAGTTTGAGACC T C SLTM Ensembl:ENSG00000137776 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1313722631 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25147950 44229 RMVar_ID_44229 Human_SNP_ID_579219191 A-to-I Human chr15 - 58883029 58883029 58883029 ATTACAGGCGGGAGCCACTGCACTCAGTCTAGATAATGAATCTTAACCTCACATTGGAACCATCA ATTACAGGCGGGAGCCACTGCACTCAGTCTAGTTAATGAATCTTAACCTCACATTGGAACCATCA T A SLTM Ensembl:ENSG00000137776 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11858989 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5014,GWAS_ID_5015,GWAS_ID_5016,GWAS_ID_5017,GWAS_ID_5018,GWAS_ID_5019,GWAS_ID_5020,GWAS_ID_5021,GWAS_ID_5022,GWAS_ID_5023,GWAS_ID_5024,GWAS_ID_5025 44230 RMVar_ID_44230 Human_SNP_ID_579219192 A-to-I Human chr15 - 58883029 58883029 58883029 ATTACAGGCGGGAGCCACTGCACTCAGTCTAGATAATGAATCTTAACCTCACATTGGAACCATCA ATTACAGGCGGGAGCCACTGCACTCAGTCTAGGTAATGAATCTTAACCTCACATTGGAACCATCA T C SLTM Ensembl:ENSG00000137776 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11858989 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5014,GWAS_ID_5015,GWAS_ID_5016,GWAS_ID_5017,GWAS_ID_5018,GWAS_ID_5019,GWAS_ID_5020,GWAS_ID_5021,GWAS_ID_5022,GWAS_ID_5023,GWAS_ID_5024,GWAS_ID_5025 44231 RMVar_ID_44231 Human_SNP_ID_579219617 A-to-I Human chr15 - 58884395 58884395 58884395 AGAATCGCTTGAATCCGGGGGGCGGAGGTTGCAGTGAGCCGAGATCGCGCCACTGCATTCCAGCC AGAATCGCTTGAATCCGGGGGGCGGAGGTTGCGGTGAGCCGAGATCGCGCCACTGCATTCCAGCC T C SLTM Ensembl:ENSG00000137776 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs958427706 Functional Loss SNV dbSNP153 33..33 33 - - - 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 44232 RMVar_ID_44232 Human_SNP_ID_579219926 A-to-I Human chr15 - 58885684 58885684 58885684 CGCCTCCCAGGTTCAAGCGATTTTCCTTCCTCAGCCTCCCGATTAGCTGGGACTACAGATGTGCG CGCCTCCCAGGTTCAAGCGATTTTCCTTCCTCGGCCTCCCGATTAGCTGGGACTACAGATGTGCG T C SLTM Ensembl:ENSG00000137776 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1211838789 Functional Loss SNV dbSNP153 33..33 33 - - - 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 44233 RMVar_ID_44233 Human_SNP_ID_579220252 A-to-I Human chr15 - 58886509 58886509 58886509 TAATCCCAACACTGTGGGAGGCCGAGGTGGGCAGATCGCCTGAGCTCAGGAATTTCAGACTAGCC TAATCCCAACACTGTGGGAGGCCGAGGTGGGCGGATCGCCTGAGCTCAGGAATTTCAGACTAGCC T C SLTM Ensembl:ENSG00000137776 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1319968343 Functional Loss SNV dbSNP153 33..33 33 - - - 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 44234 RMVar_ID_44234 Human_SNP_ID_579223554 A-to-I Human chr15 - 58899827 58899827 58899827 ACACAGCTCATGAAGAGATGGAAGCTCATACGACTGTGAAAGAAGCTGAGGATGACAACATCTCG ACACAGCTCATGAAGAGATGGAAGCTCATACGTCTGTGAAAGAAGCTGAGGATGACAACATCTCG T A SLTM Ensembl:ENSG00000137776 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1252777144 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9370972,Human_RBP_ID_12539344,Human_RBP_ID_22496434,Human_RBP_ID_22934568,Human_RBP_ID_23113773 Human_Splice_Rec_1608080,Human_Splice_Rec_1608110,Human_Splice_Rec_1608152 Human_miRNA_ID_2286179,Human_miRNA_ID_2289177 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 44235 RMVar_ID_44235 Human_SNP_ID_579226697 A-to-I Human chr15 - 58912385 58912385 58912385 TAAAACTATTGGCAAGGTCGGGCGCGCTAGGTAGCTCACGCCTGTAATCCCAGCACTTTGGGAGG TAAAACTATTGGCAAGGTCGGGCGCGCTAGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGG T C SLTM Ensembl:ENSG00000137776 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1366833950 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_122971,Human_RBP_ID_12539538,Human_RBP_ID_19069682 RMVar_hsa_circ_376047,RMVar_hsa_circ_172430,RMVar_hsa_circ_56300,RMVar_hsa_circ_47364,RMVar_hsa_circ_74124,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_315472 44236 RMVar_ID_44236 Human_SNP_ID_579229604 A-to-I Human chr15 - 58922727 58922720 58922727 GCCTGGGTGACAGAGTGAGACTCCATCTCAAAAAAAAAAGAAAAAAGAAAGATACAATGCTTGAA GCCTGGGTGACAGAGTGAGACTCCATCTCAAA_______GAAAAAAGAAAGATACAATGCTTGAA CTTTTTTT C SLTM Ensembl:ENSG00000137776 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1313428932 Functional Loss DEL dbSNP153 33..39 33 - - - RMVar_hsa_circ_172441 44237 RMVar_ID_44237 Human_SNP_ID_579229604 A-to-I Human chr15 - 58922726 58922720 58922727 CCTGGGTGACAGAGTGAGACTCCATCTCAAAAAAAAAAGAAAAAAGAAAGATACAATGCTTGAAT CCTGGGTGACAGAGTGAGACTCCATCTCAAA_______GAAAAAAGAAAGATACAATGCTTGAAT CTTTTTTT C SLTM Ensembl:ENSG00000137776 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1313428932 Functional Loss DEL dbSNP153 32..38 33 - - - RMVar_hsa_circ_172441 44238 RMVar_ID_44238 Human_SNP_ID_579229608 A-to-I Human chr15 - 58922725 58922725 58922725 CTGGGTGACAGAGTGAGACTCCATCTCAAAAAAAAAAGAAAAAAGAAAGATACAATGCTTGAATA CTGGGTGACAGAGTGAGACTCCATCTCAAAAATAAAAGAAAAAAGAAAGATACAATGCTTGAATA T A SLTM Ensembl:ENSG00000137776 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1044664352 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172441 44239 RMVar_ID_44239 Human_SNP_ID_579230332 A-to-I Human chr15 - 58925423 58925423 58925423 TGAGGCAGGAGAGTCACTTGAACCCAGGATGCAGAGGTTGCACTGAGCTGAGATTGTGCCACTGC TGAGGCAGGAGAGTCACTTGAACCCAGGATGCGGAGGTTGCACTGAGCTGAGATTGTGCCACTGC T C SLTM Ensembl:ENSG00000137776 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1433404499 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25148267 RMVar_hsa_circ_172441 44240 RMVar_ID_44240 Human_SNP_ID_579249461 A-to-I Human chr15 + 58992162 58992162 58992162 CACCTCCCGGGTTCAAGCAATTCTTCTGCGTCAGTCTCCTGAGTAGCTGGGATTACAGGAGCGCG CACCTCCCGGGTTCAAGCAATTCTTCTGCGTCTGTCTCCTGAGTAGCTGGGATTACAGGAGCGCG A T RNF111 Ensembl:ENSG00000157450 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs367940632 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172450 44241 RMVar_ID_44241 Human_SNP_ID_579249633 A-to-I Human chr15 + 58992761 58992761 58992761 AGGATGGCTTGAGCCCGGGAGGCAGAGGTTGCAATGAGCCGAGATTGTGCCACTGCATTCCAGCC AGGATGGCTTGAGCCCGGGAGGCAGAGGTTGCGATGAGCCGAGATTGTGCCACTGCATTCCAGCC A G RNF111 Ensembl:ENSG00000157450 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560470949 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172450 44242 RMVar_ID_44242 Human_SNP_ID_579262785 A-to-I Human chr15 + 59039144 59039144 59039144 GTGCCACCATACCTGGCTAATTTTTTATTTTTAGTAGAGATGAGGTTTTTCCATGTTGGTCATGC GTGCCACCATACCTGGCTAATTTTTTATTTTTGGTAGAGATGAGGTTTTTCCATGTTGGTCATGC A G RNF111 Ensembl:ENSG00000157450 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1165338273 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172455,RMVar_hsa_circ_312690,RMVar_hsa_circ_357039,RMVar_hsa_circ_370561,RMVar_hsa_circ_362161,RMVar_hsa_circ_313105,RMVar_hsa_circ_270557,RMVar_hsa_circ_172453,RMVar_hsa_circ_172454,RMVar_hsa_circ_172452 44243 RMVar_ID_44243 Human_SNP_ID_579286252 A-to-I Human chr15 - 59122345 59122345 59122345 TGGTGTGCGCCTGAGGCAGGAGAATCGCTGGAACCCGGGAGGCAGAGGCTGCAGTGAGCTGAGAT TGGTGTGCGCCTGAGGCAGGAGAATCGCTGGATCCCGGGAGGCAGAGGCTGCAGTGAGCTGAGAT T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277938785 Functional Loss SNV dbSNP153 33..33 33 - - - 44244 RMVar_ID_44244 Human_SNP_ID_579292472 A-to-I Human chr15 - 59141715 59141715 59141715 CGACTCACTGTAACCTCCATCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCT CGACTCACTGTAACCTCCATCTCCCGGGTTCAGGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCT T C MYO1E Ensembl:ENSG00000157483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1395264765 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 44245 RMVar_ID_44245 Human_SNP_ID_579292473 A-to-I Human chr15 - 59141715 59141715 59141715 CGACTCACTGTAACCTCCATCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCT CGACTCACTGTAACCTCCATCTCCCGGGTTCACGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCT T G MYO1E Ensembl:ENSG00000157483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1395264765 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 44246 RMVar_ID_44246 Human_SNP_ID_579300139 A-to-I Human chr15 - 59167744 59167744 59167744 TGAGCCCAGGAGGCGGAGGGTGCAGTGAGCCAAGATCACACCACTGCACTCCAGCCTGGGCAACA TGAGCCCAGGAGGCGGAGGGTGCAGTGAGCCAGGATCACACCACTGCACTCCAGCCTGGGCAACA T C MYO1E Ensembl:ENSG00000157483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs894604674 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4785,RMVar_hsa_circ_172479,RMVar_hsa_circ_123105,RMVar_hsa_circ_127410,RMVar_hsa_circ_127264,RMVar_hsa_circ_122506,RMVar_hsa_circ_172483,RMVar_hsa_circ_105799,RMVar_hsa_circ_92316,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_102320,RMVar_hsa_circ_324924,RMVar_hsa_circ_172488,RMVar_hsa_circ_172489,RMVar_hsa_circ_369909,RMVar_hsa_circ_353320,RMVar_hsa_circ_275935,RMVar_hsa_circ_81330,RMVar_hsa_circ_97205,RMVar_hsa_circ_43360,RMVar_hsa_circ_64845,RMVar_hsa_circ_103072,RMVar_hsa_circ_172491,RMVar_hsa_circ_172493,RMVar_hsa_circ_172494,RMVar_hsa_circ_172492,RMVar_hsa_circ_172490,RMVar_hsa_circ_95167,RMVar_hsa_circ_97210,RMVar_hsa_circ_93592,RMVar_hsa_circ_172498,RMVar_hsa_circ_172500,RMVar_hsa_circ_63849,RMVar_hsa_circ_172499,RMVar_hsa_circ_172497,RMVar_hsa_circ_58138,RMVar_hsa_circ_121884,RMVar_hsa_circ_269227,RMVar_hsa_circ_91359,RMVar_hsa_circ_172501,RMVar_hsa_circ_356200,RMVar_hsa_circ_86231,RMVar_hsa_circ_172502,RMVar_hsa_circ_172503 44247 RMVar_ID_44247 Human_SNP_ID_579300309 A-to-I Human chr15 - 59168398 59168398 59168398 GAGACTACAGGCATGTACCCCCACTTCTGGCTAATTTTTGTATTTTTTGTAGAGACACGGTTTCC GAGACTACAGGCATGTACCCCCACTTCTGGCTGATTTTTGTATTTTTTGTAGAGACACGGTTTCC T C MYO1E Ensembl:ENSG00000157483 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1319707783 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4785,RMVar_hsa_circ_172479,RMVar_hsa_circ_123105,RMVar_hsa_circ_127410,RMVar_hsa_circ_127264,RMVar_hsa_circ_122506,RMVar_hsa_circ_172483,RMVar_hsa_circ_105799,RMVar_hsa_circ_92316,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_102320,RMVar_hsa_circ_324924,RMVar_hsa_circ_172488,RMVar_hsa_circ_172489,RMVar_hsa_circ_369909,RMVar_hsa_circ_353320,RMVar_hsa_circ_275935,RMVar_hsa_circ_81330,RMVar_hsa_circ_97205,RMVar_hsa_circ_43360,RMVar_hsa_circ_64845,RMVar_hsa_circ_103072,RMVar_hsa_circ_172491,RMVar_hsa_circ_172493,RMVar_hsa_circ_172494,RMVar_hsa_circ_172492,RMVar_hsa_circ_172490,RMVar_hsa_circ_95167,RMVar_hsa_circ_97210,RMVar_hsa_circ_93592,RMVar_hsa_circ_172498,RMVar_hsa_circ_172500,RMVar_hsa_circ_63849,RMVar_hsa_circ_172499,RMVar_hsa_circ_172497,RMVar_hsa_circ_58138,RMVar_hsa_circ_121884,RMVar_hsa_circ_269227,RMVar_hsa_circ_91359,RMVar_hsa_circ_172501,RMVar_hsa_circ_356200,RMVar_hsa_circ_86231,RMVar_hsa_circ_172502,RMVar_hsa_circ_172503 44248 RMVar_ID_44248 Human_SNP_ID_579300381 A-to-I Human chr15 - 59168696 59168696 59168696 GGATTGCTTGAGCCCAATAGGTCAAGGCTGCAATGAGTCATGATCATACCACTGCACTCCAGCCT GGATTGCTTGAGCCCAATAGGTCAAGGCTGCAGTGAGTCATGATCATACCACTGCACTCCAGCCT T C MYO1E Ensembl:ENSG00000157483 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs901998304 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4785,RMVar_hsa_circ_172479,RMVar_hsa_circ_123105,RMVar_hsa_circ_127410,RMVar_hsa_circ_127264,RMVar_hsa_circ_122506,RMVar_hsa_circ_172483,RMVar_hsa_circ_105799,RMVar_hsa_circ_92316,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_102320,RMVar_hsa_circ_324924,RMVar_hsa_circ_172488,RMVar_hsa_circ_172489,RMVar_hsa_circ_369909,RMVar_hsa_circ_353320,RMVar_hsa_circ_275935,RMVar_hsa_circ_81330,RMVar_hsa_circ_97205,RMVar_hsa_circ_43360,RMVar_hsa_circ_64845,RMVar_hsa_circ_103072,RMVar_hsa_circ_172491,RMVar_hsa_circ_172493,RMVar_hsa_circ_172494,RMVar_hsa_circ_172492,RMVar_hsa_circ_172490,RMVar_hsa_circ_95167,RMVar_hsa_circ_97210,RMVar_hsa_circ_93592,RMVar_hsa_circ_172498,RMVar_hsa_circ_172500,RMVar_hsa_circ_63849,RMVar_hsa_circ_172499,RMVar_hsa_circ_172497,RMVar_hsa_circ_58138,RMVar_hsa_circ_121884,RMVar_hsa_circ_269227,RMVar_hsa_circ_91359,RMVar_hsa_circ_172501,RMVar_hsa_circ_356200,RMVar_hsa_circ_86231,RMVar_hsa_circ_172502,RMVar_hsa_circ_172503 44249 RMVar_ID_44249 Human_SNP_ID_579300393 A-to-I Human chr15 - 59168745 59168745 59168745 GTGGTGGTACGTGCCCGTGGTCCCAGCTACTCAGGAAGCTGAGGTGGGAGGATTGCTTGAGCCCA GTGGTGGTACGTGCCCGTGGTCCCAGCTACTCGGGAAGCTGAGGTGGGAGGATTGCTTGAGCCCA T C MYO1E Ensembl:ENSG00000157483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1160549114 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4785,RMVar_hsa_circ_172479,RMVar_hsa_circ_123105,RMVar_hsa_circ_127410,RMVar_hsa_circ_127264,RMVar_hsa_circ_122506,RMVar_hsa_circ_172483,RMVar_hsa_circ_105799,RMVar_hsa_circ_92316,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_102320,RMVar_hsa_circ_324924,RMVar_hsa_circ_172488,RMVar_hsa_circ_172489,RMVar_hsa_circ_369909,RMVar_hsa_circ_353320,RMVar_hsa_circ_275935,RMVar_hsa_circ_81330,RMVar_hsa_circ_97205,RMVar_hsa_circ_43360,RMVar_hsa_circ_64845,RMVar_hsa_circ_103072,RMVar_hsa_circ_172491,RMVar_hsa_circ_172493,RMVar_hsa_circ_172494,RMVar_hsa_circ_172492,RMVar_hsa_circ_172490,RMVar_hsa_circ_95167,RMVar_hsa_circ_97210,RMVar_hsa_circ_93592,RMVar_hsa_circ_172498,RMVar_hsa_circ_172500,RMVar_hsa_circ_63849,RMVar_hsa_circ_172499,RMVar_hsa_circ_172497,RMVar_hsa_circ_58138,RMVar_hsa_circ_121884,RMVar_hsa_circ_269227,RMVar_hsa_circ_91359,RMVar_hsa_circ_172501,RMVar_hsa_circ_356200,RMVar_hsa_circ_86231,RMVar_hsa_circ_172502,RMVar_hsa_circ_172503 44250 RMVar_ID_44250 Human_SNP_ID_579300451 A-to-I Human chr15 - 59168954 59168954 59168954 AATTTTAATATAAAGAGACTTTATCTTTTAATAATATGTACTGAAACATTTGAGCATGAAATAAA AATTTTAATATAAAGAGACTTTATCTTTTAATGATATGTACTGAAACATTTGAGCATGAAATAAA T C MYO1E Ensembl:ENSG00000157483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11071410 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4785,RMVar_hsa_circ_172479,RMVar_hsa_circ_123105,RMVar_hsa_circ_127410,RMVar_hsa_circ_127264,RMVar_hsa_circ_122506,RMVar_hsa_circ_172483,RMVar_hsa_circ_105799,RMVar_hsa_circ_92316,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_102320,RMVar_hsa_circ_324924,RMVar_hsa_circ_172488,RMVar_hsa_circ_172489,RMVar_hsa_circ_369909,RMVar_hsa_circ_353320,RMVar_hsa_circ_275935,RMVar_hsa_circ_81330,RMVar_hsa_circ_97205,RMVar_hsa_circ_43360,RMVar_hsa_circ_64845,RMVar_hsa_circ_103072,RMVar_hsa_circ_172491,RMVar_hsa_circ_172493,RMVar_hsa_circ_172494,RMVar_hsa_circ_172492,RMVar_hsa_circ_172490,RMVar_hsa_circ_95167,RMVar_hsa_circ_97210,RMVar_hsa_circ_93592,RMVar_hsa_circ_172498,RMVar_hsa_circ_172500,RMVar_hsa_circ_63849,RMVar_hsa_circ_172499,RMVar_hsa_circ_172497,RMVar_hsa_circ_58138,RMVar_hsa_circ_121884,RMVar_hsa_circ_269227,RMVar_hsa_circ_91359,RMVar_hsa_circ_172501,RMVar_hsa_circ_356200,RMVar_hsa_circ_86231,RMVar_hsa_circ_172502,RMVar_hsa_circ_172503 44251 RMVar_ID_44251 Human_SNP_ID_579300961 A-to-I Human chr15 - 59170731 59170731 59170731 TTCTATCTGTTCCTAATTTCCCTGGATAAAGGACCAGGCAGTGCAGTGCAGTGAAGTATTTAAAA TTCTATCTGTTCCTAATTTCCCTGGATAAAGGGCCAGGCAGTGCAGTGCAGTGAAGTATTTAAAA T C MYO1E Ensembl:ENSG00000157483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10775168 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5026,GWAS_ID_5027,GWAS_ID_5028,GWAS_ID_5029,GWAS_ID_5030 RMVar_hsa_circ_4785,RMVar_hsa_circ_172479,RMVar_hsa_circ_123105,RMVar_hsa_circ_127410,RMVar_hsa_circ_127264,RMVar_hsa_circ_122506,RMVar_hsa_circ_172483,RMVar_hsa_circ_105799,RMVar_hsa_circ_92316,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_102320,RMVar_hsa_circ_324924,RMVar_hsa_circ_172488,RMVar_hsa_circ_172489,RMVar_hsa_circ_369909,RMVar_hsa_circ_353320,RMVar_hsa_circ_275935,RMVar_hsa_circ_81330,RMVar_hsa_circ_97205,RMVar_hsa_circ_43360,RMVar_hsa_circ_64845,RMVar_hsa_circ_103072,RMVar_hsa_circ_172491,RMVar_hsa_circ_172493,RMVar_hsa_circ_172494,RMVar_hsa_circ_172492,RMVar_hsa_circ_172490,RMVar_hsa_circ_95167,RMVar_hsa_circ_97210,RMVar_hsa_circ_93592,RMVar_hsa_circ_172498,RMVar_hsa_circ_172500,RMVar_hsa_circ_63849,RMVar_hsa_circ_172499,RMVar_hsa_circ_172497,RMVar_hsa_circ_58138,RMVar_hsa_circ_121884,RMVar_hsa_circ_269227,RMVar_hsa_circ_91359,RMVar_hsa_circ_172501,RMVar_hsa_circ_356200,RMVar_hsa_circ_86231,RMVar_hsa_circ_172502,RMVar_hsa_circ_172503 44252 RMVar_ID_44252 Human_SNP_ID_579301149 A-to-I Human chr15 - 59171396 59171396 59171396 TGGAGTCATCGTGAGATGCTCTCTTCGCTCCAATTCTCAGGCAGTGGGGAGTGGTGTTTGCTTCC TGGAGTCATCGTGAGATGCTCTCTTCGCTCCAGTTCTCAGGCAGTGGGGAGTGGTGTTTGCTTCC T C MYO1E Ensembl:ENSG00000157483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6494072 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5031,GWAS_ID_5032,GWAS_ID_5033 RMVar_hsa_circ_4785,RMVar_hsa_circ_172479,RMVar_hsa_circ_123105,RMVar_hsa_circ_127410,RMVar_hsa_circ_127264,RMVar_hsa_circ_122506,RMVar_hsa_circ_172483,RMVar_hsa_circ_105799,RMVar_hsa_circ_92316,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_102320,RMVar_hsa_circ_324924,RMVar_hsa_circ_172488,RMVar_hsa_circ_172489,RMVar_hsa_circ_369909,RMVar_hsa_circ_353320,RMVar_hsa_circ_275935,RMVar_hsa_circ_81330,RMVar_hsa_circ_97205,RMVar_hsa_circ_43360,RMVar_hsa_circ_64845,RMVar_hsa_circ_103072,RMVar_hsa_circ_172491,RMVar_hsa_circ_172493,RMVar_hsa_circ_172494,RMVar_hsa_circ_172492,RMVar_hsa_circ_172490,RMVar_hsa_circ_95167,RMVar_hsa_circ_97210,RMVar_hsa_circ_93592,RMVar_hsa_circ_172498,RMVar_hsa_circ_172500,RMVar_hsa_circ_63849,RMVar_hsa_circ_172499,RMVar_hsa_circ_172497,RMVar_hsa_circ_58138,RMVar_hsa_circ_121884,RMVar_hsa_circ_269227,RMVar_hsa_circ_91359,RMVar_hsa_circ_172501,RMVar_hsa_circ_356200,RMVar_hsa_circ_86231,RMVar_hsa_circ_172502,RMVar_hsa_circ_172503 44253 RMVar_ID_44253 Human_SNP_ID_579312455 A-to-I Human chr15 - 59209973 59209973 59209973 AAAATTAGCCAGGCATGGTGGCACGCACCTGTAGTCCCAGCTACTCTGGAGGCTGAGGTGGGAGG AAAATTAGCCAGGCATGGTGGCACGCACCTGTGGTCCCAGCTACTCTGGAGGCTGAGGTGGGAGG T C MYO1E Ensembl:ENSG00000157483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1566979797 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172479,RMVar_hsa_circ_127410,RMVar_hsa_circ_127264,RMVar_hsa_circ_122506,RMVar_hsa_circ_105799,RMVar_hsa_circ_172481,RMVar_hsa_circ_172480,RMVar_hsa_circ_90542,RMVar_hsa_circ_124143,RMVar_hsa_circ_172478,RMVar_hsa_circ_172488,RMVar_hsa_circ_172489,RMVar_hsa_circ_353320,RMVar_hsa_circ_275935,RMVar_hsa_circ_81330,RMVar_hsa_circ_43360,RMVar_hsa_circ_4585,RMVar_hsa_circ_64845,RMVar_hsa_circ_103072,RMVar_hsa_circ_172491,RMVar_hsa_circ_172490,RMVar_hsa_circ_95167,RMVar_hsa_circ_97210,RMVar_hsa_circ_93592,RMVar_hsa_circ_172498,RMVar_hsa_circ_172500,RMVar_hsa_circ_63849,RMVar_hsa_circ_172499,RMVar_hsa_circ_172497,RMVar_hsa_circ_58138,RMVar_hsa_circ_121884,RMVar_hsa_circ_91359,RMVar_hsa_circ_172501,RMVar_hsa_circ_86231,RMVar_hsa_circ_74087,RMVar_hsa_circ_343427,RMVar_hsa_circ_172502,RMVar_hsa_circ_172503,RMVar_hsa_circ_352263,RMVar_hsa_circ_351796,RMVar_hsa_circ_110466,RMVar_hsa_circ_81693,RMVar_hsa_circ_68913,RMVar_hsa_circ_90991,RMVar_hsa_circ_172505,RMVar_hsa_circ_172506,RMVar_hsa_circ_323571,RMVar_hsa_circ_12931,RMVar_hsa_circ_266654,RMVar_hsa_circ_309475,RMVar_hsa_circ_172507,RMVar_hsa_circ_362278,RMVar_hsa_circ_52199,RMVar_hsa_circ_101518,RMVar_hsa_circ_313716,RMVar_hsa_circ_290217,RMVar_hsa_circ_51197,RMVar_hsa_circ_172514,RMVar_hsa_circ_99993,RMVar_hsa_circ_172510,RMVar_hsa_circ_172511,RMVar_hsa_circ_172512,RMVar_hsa_circ_316721,RMVar_hsa_circ_270002,RMVar_hsa_circ_62270,RMVar_hsa_circ_172515,RMVar_hsa_circ_100869,RMVar_hsa_circ_274521,RMVar_hsa_circ_340406,RMVar_hsa_circ_172513,RMVar_hsa_circ_364070,RMVar_hsa_circ_330610,RMVar_hsa_circ_366005,RMVar_hsa_circ_172516,RMVar_hsa_circ_370358,RMVar_hsa_circ_353678,RMVar_hsa_circ_172518,RMVar_hsa_circ_172520,RMVar_hsa_circ_75547,RMVar_hsa_circ_172519,RMVar_hsa_circ_362527,RMVar_hsa_circ_172517 44254 RMVar_ID_44254 Human_SNP_ID_579313539 A-to-I Human chr15 - 59213460 59213460 59213460 CTCTATCTCAAAAATAAATAATAGCCAGGCGCAGTGGCTCATGCCTGTAATCCCTGCACTTTGGG CTCTATCTCAAAAATAAATAATAGCCAGGCGCTGTGGCTCATGCCTGTAATCCCTGCACTTTGGG T A MYO1E Ensembl:ENSG00000157483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1455156825 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172479,RMVar_hsa_circ_127410,RMVar_hsa_circ_127264,RMVar_hsa_circ_122506,RMVar_hsa_circ_105799,RMVar_hsa_circ_172481,RMVar_hsa_circ_172480,RMVar_hsa_circ_90542,RMVar_hsa_circ_124143,RMVar_hsa_circ_172478,RMVar_hsa_circ_172488,RMVar_hsa_circ_172489,RMVar_hsa_circ_353320,RMVar_hsa_circ_275935,RMVar_hsa_circ_81330,RMVar_hsa_circ_43360,RMVar_hsa_circ_4585,RMVar_hsa_circ_64845,RMVar_hsa_circ_103072,RMVar_hsa_circ_172491,RMVar_hsa_circ_172490,RMVar_hsa_circ_95167,RMVar_hsa_circ_97210,RMVar_hsa_circ_93592,RMVar_hsa_circ_172498,RMVar_hsa_circ_172500,RMVar_hsa_circ_63849,RMVar_hsa_circ_172499,RMVar_hsa_circ_172497,RMVar_hsa_circ_58138,RMVar_hsa_circ_121884,RMVar_hsa_circ_91359,RMVar_hsa_circ_172501,RMVar_hsa_circ_86231,RMVar_hsa_circ_74087,RMVar_hsa_circ_343427,RMVar_hsa_circ_172502,RMVar_hsa_circ_172503,RMVar_hsa_circ_352263,RMVar_hsa_circ_351796,RMVar_hsa_circ_110466,RMVar_hsa_circ_81693,RMVar_hsa_circ_68913,RMVar_hsa_circ_90991,RMVar_hsa_circ_172505,RMVar_hsa_circ_172506,RMVar_hsa_circ_323571,RMVar_hsa_circ_12931,RMVar_hsa_circ_266654,RMVar_hsa_circ_309475,RMVar_hsa_circ_172507,RMVar_hsa_circ_52199,RMVar_hsa_circ_101518,RMVar_hsa_circ_313716,RMVar_hsa_circ_290217,RMVar_hsa_circ_55085,RMVar_hsa_circ_172514,RMVar_hsa_circ_99993,RMVar_hsa_circ_172510,RMVar_hsa_circ_172511,RMVar_hsa_circ_172512,RMVar_hsa_circ_316721,RMVar_hsa_circ_270002,RMVar_hsa_circ_172515,RMVar_hsa_circ_100869,RMVar_hsa_circ_274521,RMVar_hsa_circ_340406,RMVar_hsa_circ_172513,RMVar_hsa_circ_364070,RMVar_hsa_circ_172516,RMVar_hsa_circ_370358,RMVar_hsa_circ_353678,RMVar_hsa_circ_172518,RMVar_hsa_circ_172520,RMVar_hsa_circ_75547,RMVar_hsa_circ_172519,RMVar_hsa_circ_362527,RMVar_hsa_circ_172517,RMVar_hsa_circ_368152,RMVar_hsa_circ_172521 44255 RMVar_ID_44255 Human_SNP_ID_579315938 A-to-I Human chr15 - 59220337 59220337 59220337 TCAAGCAGTTCTCCTGTCTCAGCCTCCCAAGTAGCTGGGATTACAGGTGCGCACCACCACGCCTG TCAAGCAGTTCTCCTGTCTCAGCCTCCCAAGTGGCTGGGATTACAGGTGCGCACCACCACGCCTG T C MYO1E Ensembl:ENSG00000157483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs554548842 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_172479,RMVar_hsa_circ_127264,RMVar_hsa_circ_122506,RMVar_hsa_circ_124143,RMVar_hsa_circ_172478,RMVar_hsa_circ_172489,RMVar_hsa_circ_81330,RMVar_hsa_circ_43360,RMVar_hsa_circ_4585,RMVar_hsa_circ_103072,RMVar_hsa_circ_172490,RMVar_hsa_circ_95167,RMVar_hsa_circ_97210,RMVar_hsa_circ_93592,RMVar_hsa_circ_172498,RMVar_hsa_circ_172500,RMVar_hsa_circ_172499,RMVar_hsa_circ_172497,RMVar_hsa_circ_121884,RMVar_hsa_circ_91359,RMVar_hsa_circ_172501,RMVar_hsa_circ_86231,RMVar_hsa_circ_74087,RMVar_hsa_circ_172502,RMVar_hsa_circ_172503,RMVar_hsa_circ_351796,RMVar_hsa_circ_110466,RMVar_hsa_circ_81693,RMVar_hsa_circ_90991,RMVar_hsa_circ_172505,RMVar_hsa_circ_172506,RMVar_hsa_circ_12931,RMVar_hsa_circ_266654,RMVar_hsa_circ_172507,RMVar_hsa_circ_101518,RMVar_hsa_circ_99993,RMVar_hsa_circ_172512,RMVar_hsa_circ_100869,RMVar_hsa_circ_172513,RMVar_hsa_circ_370358,RMVar_hsa_circ_172520,RMVar_hsa_circ_172519,RMVar_hsa_circ_25472,RMVar_hsa_circ_13901,RMVar_hsa_circ_317815,RMVar_hsa_circ_337598,RMVar_hsa_circ_369028,RMVar_hsa_circ_296513,RMVar_hsa_circ_172522,RMVar_hsa_circ_172524,RMVar_hsa_circ_8552,RMVar_hsa_circ_172523 44256 RMVar_ID_44256 Human_SNP_ID_579316251 A-to-I Human chr15 - 59221224 59221224 59221224 AGGTGATCACCTGAGGTCAGGAGTTTGAAACCAGCCTGGCCAACATGGTGAAATCCTGTCTCTAC AGGTGATCACCTGAGGTCAGGAGTTTGAAACCGGCCTGGCCAACATGGTGAAATCCTGTCTCTAC T C MYO1E Ensembl:ENSG00000157483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1006452193 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12541477 RMVar_hsa_circ_172479,RMVar_hsa_circ_127264,RMVar_hsa_circ_122506,RMVar_hsa_circ_124143,RMVar_hsa_circ_172478,RMVar_hsa_circ_172489,RMVar_hsa_circ_81330,RMVar_hsa_circ_43360,RMVar_hsa_circ_4585,RMVar_hsa_circ_103072,RMVar_hsa_circ_172490,RMVar_hsa_circ_95167,RMVar_hsa_circ_97210,RMVar_hsa_circ_93592,RMVar_hsa_circ_172498,RMVar_hsa_circ_172500,RMVar_hsa_circ_172499,RMVar_hsa_circ_172497,RMVar_hsa_circ_121884,RMVar_hsa_circ_91359,RMVar_hsa_circ_172501,RMVar_hsa_circ_86231,RMVar_hsa_circ_74087,RMVar_hsa_circ_172502,RMVar_hsa_circ_172503,RMVar_hsa_circ_351796,RMVar_hsa_circ_110466,RMVar_hsa_circ_81693,RMVar_hsa_circ_90991,RMVar_hsa_circ_172505,RMVar_hsa_circ_172506,RMVar_hsa_circ_12931,RMVar_hsa_circ_266654,RMVar_hsa_circ_172507,RMVar_hsa_circ_101518,RMVar_hsa_circ_99993,RMVar_hsa_circ_172512,RMVar_hsa_circ_100869,RMVar_hsa_circ_172513,RMVar_hsa_circ_370358,RMVar_hsa_circ_172520,RMVar_hsa_circ_172519,RMVar_hsa_circ_25472,RMVar_hsa_circ_13901,RMVar_hsa_circ_317815,RMVar_hsa_circ_337598,RMVar_hsa_circ_369028,RMVar_hsa_circ_296513,RMVar_hsa_circ_172522,RMVar_hsa_circ_172524,RMVar_hsa_circ_8552,RMVar_hsa_circ_172523 44257 RMVar_ID_44257 Human_SNP_ID_579317937 A-to-I Human chr15 - 59226624 59226624 59226624 TTTTGTATTTTTCGTAGAGGTGGGGTTTCACCATGTTACCCAGGTTGGTCTCTAACTCTCGGACT TTTTGTATTTTTCGTAGAGGTGGGGTTTCACCGTGTTACCCAGGTTGGTCTCTAACTCTCGGACT T C MYO1E Ensembl:ENSG00000157483 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs983605721 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122506,RMVar_hsa_circ_124143,RMVar_hsa_circ_172478,RMVar_hsa_circ_172489,RMVar_hsa_circ_81330,RMVar_hsa_circ_43360,RMVar_hsa_circ_103072,RMVar_hsa_circ_172490,RMVar_hsa_circ_97210,RMVar_hsa_circ_93592,RMVar_hsa_circ_172498,RMVar_hsa_circ_172500,RMVar_hsa_circ_172499,RMVar_hsa_circ_91359,RMVar_hsa_circ_172502,RMVar_hsa_circ_351796,RMVar_hsa_circ_110466,RMVar_hsa_circ_81693,RMVar_hsa_circ_172505,RMVar_hsa_circ_172506,RMVar_hsa_circ_12931,RMVar_hsa_circ_266654,RMVar_hsa_circ_99993,RMVar_hsa_circ_100869,RMVar_hsa_circ_172513,RMVar_hsa_circ_370358,RMVar_hsa_circ_172520,RMVar_hsa_circ_172519,RMVar_hsa_circ_41831,RMVar_hsa_circ_25472,RMVar_hsa_circ_337598,RMVar_hsa_circ_369028,RMVar_hsa_circ_296513,RMVar_hsa_circ_172522,RMVar_hsa_circ_8552,RMVar_hsa_circ_172523,RMVar_hsa_circ_172525,RMVar_hsa_circ_374211,RMVar_hsa_circ_378330,RMVar_hsa_circ_359618,RMVar_hsa_circ_70552 44258 RMVar_ID_44258 Human_SNP_ID_579319873 A-to-I Human chr15 - 59233195 59233195 59233195 CACTGTAATTTAAAAAGGGAAAAGATAGAAGAAGATTCTGGCTTTTGTTCTCTTCCTGAGAGAAG CACTGTAATTTAAAAAGGGAAAAGATAGAAGATGATTCTGGCTTTTGTTCTCTTCCTGAGAGAAG T A MYO1E Ensembl:ENSG00000157483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1236050661 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122506,RMVar_hsa_circ_124143,RMVar_hsa_circ_172478,RMVar_hsa_circ_172489,RMVar_hsa_circ_81330,RMVar_hsa_circ_43360,RMVar_hsa_circ_103072,RMVar_hsa_circ_172490,RMVar_hsa_circ_97210,RMVar_hsa_circ_93592,RMVar_hsa_circ_172498,RMVar_hsa_circ_172500,RMVar_hsa_circ_172499,RMVar_hsa_circ_351796,RMVar_hsa_circ_110466,RMVar_hsa_circ_172506,RMVar_hsa_circ_12931,RMVar_hsa_circ_99993,RMVar_hsa_circ_100869,RMVar_hsa_circ_172513,RMVar_hsa_circ_172520,RMVar_hsa_circ_41831,RMVar_hsa_circ_25472,RMVar_hsa_circ_337598,RMVar_hsa_circ_296513,RMVar_hsa_circ_172522,RMVar_hsa_circ_172525,RMVar_hsa_circ_374211,RMVar_hsa_circ_359618,RMVar_hsa_circ_60511,RMVar_hsa_circ_172527,RMVar_hsa_circ_371653 44259 RMVar_ID_44259 Human_SNP_ID_579319913 A-to-I Human chr15 - 59233339 59233339 59233339 TTTTACCTCAGTTTGCTCTTTCTCTTTTCCCTAATATGCCCGCCACATGCCACAAAATTCTGTTG TTTTACCTCAGTTTGCTCTTTCTCTTTTCCCTGATATGCCCGCCACATGCCACAAAATTCTGTTG T C MYO1E Ensembl:ENSG00000157483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1177347901 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122506,RMVar_hsa_circ_124143,RMVar_hsa_circ_172478,RMVar_hsa_circ_172489,RMVar_hsa_circ_81330,RMVar_hsa_circ_43360,RMVar_hsa_circ_103072,RMVar_hsa_circ_172490,RMVar_hsa_circ_97210,RMVar_hsa_circ_93592,RMVar_hsa_circ_172498,RMVar_hsa_circ_172500,RMVar_hsa_circ_172499,RMVar_hsa_circ_351796,RMVar_hsa_circ_110466,RMVar_hsa_circ_172506,RMVar_hsa_circ_12931,RMVar_hsa_circ_99993,RMVar_hsa_circ_100869,RMVar_hsa_circ_172513,RMVar_hsa_circ_172520,RMVar_hsa_circ_41831,RMVar_hsa_circ_25472,RMVar_hsa_circ_337598,RMVar_hsa_circ_296513,RMVar_hsa_circ_172522,RMVar_hsa_circ_172525,RMVar_hsa_circ_374211,RMVar_hsa_circ_359618,RMVar_hsa_circ_60511,RMVar_hsa_circ_172527,RMVar_hsa_circ_371653 44260 RMVar_ID_44260 Human_SNP_ID_579320251 A-to-I Human chr15 - 59234205 59234205 59234205 CCATCCATCCATCCATCCATCCATCAGTGATCAGTGATGTCCAACAGAATTTTGTGGCATGTGGT CCATCCATCCATCCATCCATCCATCAGTGATCGGTGATGTCCAACAGAATTTTGTGGCATGTGGT T C MYO1E Ensembl:ENSG00000157483 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1486636029 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12541534 RMVar_hsa_circ_122506,RMVar_hsa_circ_124143,RMVar_hsa_circ_172478,RMVar_hsa_circ_172489,RMVar_hsa_circ_81330,RMVar_hsa_circ_43360,RMVar_hsa_circ_103072,RMVar_hsa_circ_172490,RMVar_hsa_circ_97210,RMVar_hsa_circ_93592,RMVar_hsa_circ_172498,RMVar_hsa_circ_172500,RMVar_hsa_circ_172499,RMVar_hsa_circ_351796,RMVar_hsa_circ_110466,RMVar_hsa_circ_172506,RMVar_hsa_circ_12931,RMVar_hsa_circ_99993,RMVar_hsa_circ_100869,RMVar_hsa_circ_172513,RMVar_hsa_circ_172520,RMVar_hsa_circ_41831,RMVar_hsa_circ_25472,RMVar_hsa_circ_337598,RMVar_hsa_circ_296513,RMVar_hsa_circ_172522,RMVar_hsa_circ_172525,RMVar_hsa_circ_374211,RMVar_hsa_circ_359618,RMVar_hsa_circ_60511,RMVar_hsa_circ_172527,RMVar_hsa_circ_371653 44261 RMVar_ID_44261 Human_SNP_ID_579329419 A-to-I Human chr15 - 59265771 59265771 59265771 TTTTTTTTTTTAAGGAGATGGGGTCTCAGTATATTGCCCAGGCTGGTCTCGAACTCCTGGACTCA TTTTTTTTTTTAAGGAGATGGGGTCTCAGTATCTTGCCCAGGCTGGTCTCGAACTCCTGGACTCA T G MYO1E Ensembl:ENSG00000157483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1472840279 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81330,RMVar_hsa_circ_103072,RMVar_hsa_circ_172490,RMVar_hsa_circ_93592,RMVar_hsa_circ_172500,RMVar_hsa_circ_172499,RMVar_hsa_circ_110466,RMVar_hsa_circ_172506,RMVar_hsa_circ_100869,RMVar_hsa_circ_172520,RMVar_hsa_circ_337598,RMVar_hsa_circ_172525,RMVar_hsa_circ_374211,RMVar_hsa_circ_172528,RMVar_hsa_circ_298641 44262 RMVar_ID_44262 Human_SNP_ID_579331002 A-to-I Human chr15 - 59270461 59270461 59270461 CCAGCTCACTGCAACCTCCGCCTCCCCGGCTCAGGTGATCTTCCCACCTCAGCCTCCCAAGTAGC CCAGCTCACTGCAACCTCCGCCTCCCCGGCTCGGGTGATCTTCCCACCTCAGCCTCCCAAGTAGC T C AC092756.1,MYO1E Ensembl:ENSG00000259771,Ensembl:ENSG00000157483 lincRNA,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs539282406 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81330,RMVar_hsa_circ_103072,RMVar_hsa_circ_172490,RMVar_hsa_circ_93592,RMVar_hsa_circ_172500,RMVar_hsa_circ_172499,RMVar_hsa_circ_110466,RMVar_hsa_circ_172506,RMVar_hsa_circ_100869,RMVar_hsa_circ_172520,RMVar_hsa_circ_337598,RMVar_hsa_circ_172525,RMVar_hsa_circ_374211,RMVar_hsa_circ_172528,RMVar_hsa_circ_298641 44263 RMVar_ID_44263 Human_SNP_ID_579331003 A-to-I Human chr15 - 59270461 59270461 59270461 CCAGCTCACTGCAACCTCCGCCTCCCCGGCTCAGGTGATCTTCCCACCTCAGCCTCCCAAGTAGC CCAGCTCACTGCAACCTCCGCCTCCCCGGCTCCGGTGATCTTCCCACCTCAGCCTCCCAAGTAGC T G AC092756.1,MYO1E Ensembl:ENSG00000259771,Ensembl:ENSG00000157483 lincRNA,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs539282406 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81330,RMVar_hsa_circ_103072,RMVar_hsa_circ_172490,RMVar_hsa_circ_93592,RMVar_hsa_circ_172500,RMVar_hsa_circ_172499,RMVar_hsa_circ_110466,RMVar_hsa_circ_172506,RMVar_hsa_circ_100869,RMVar_hsa_circ_172520,RMVar_hsa_circ_337598,RMVar_hsa_circ_172525,RMVar_hsa_circ_374211,RMVar_hsa_circ_172528,RMVar_hsa_circ_298641 44264 RMVar_ID_44264 Human_SNP_ID_579331834 A-to-I Human chr15 - 59273455 59273455 59273455 TGTTATTGACGCATGAATCACTTTATTCCATCATTATCTAGGTGTCCTTCAAGGGACTTTGAACT TGTTATTGACGCATGAATCACTTTATTCCATCCTTATCTAGGTGTCCTTCAAGGGACTTTGAACT T G MYO1E Ensembl:ENSG00000157483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs527398903 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2448109,Human_RBP_ID_25148722 RMVar_hsa_circ_81330,RMVar_hsa_circ_172490,RMVar_hsa_circ_93592,RMVar_hsa_circ_172500 44265 RMVar_ID_44265 Human_SNP_ID_579340492 A-to-I Human chr15 - 59303299 59303299 59303299 GTGATTCTCCCATCTCAGGCTCCCAAGTAGCTAGAACTACAGGCACATGCCACCACCACACCCGG GTGATTCTCCCATCTCAGGCTCCCAAGTAGCTGGAACTACAGGCACATGCCACCACCACACCCGG T C MYO1E Ensembl:ENSG00000157483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs550640749 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81330,RMVar_hsa_circ_172490,RMVar_hsa_circ_93592,RMVar_hsa_circ_172500 44266 RMVar_ID_44266 Human_SNP_ID_579340502 A-to-I Human chr15 - 59303345 59303345 59303345 CTATGGCACAATCCCGTCTCACTGCAGCCTCGACCTCCTGGCTCAGGTGATTCTCCCATCTCAGG CTATGGCACAATCCCGTCTCACTGCAGCCTCGGCCTCCTGGCTCAGGTGATTCTCCCATCTCAGG T C MYO1E Ensembl:ENSG00000157483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs981108959 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81330,RMVar_hsa_circ_172490,RMVar_hsa_circ_93592,RMVar_hsa_circ_172500 44267 RMVar_ID_44267 Human_SNP_ID_579341077 A-to-I Human chr15 - 59305326 59305326 59305326 AGCCGGGCATGGTGGTGTGTGCTTGTAGTCCCAACTACTCAGAAGGCCGAGGTGGGAGGATTGCT AGCCGGGCATGGTGGTGTGTGCTTGTAGTCCCTACTACTCAGAAGGCCGAGGTGGGAGGATTGCT T A MYO1E Ensembl:ENSG00000157483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1222239173 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81330,RMVar_hsa_circ_172490,RMVar_hsa_circ_93592,RMVar_hsa_circ_172500 44268 RMVar_ID_44268 Human_SNP_ID_579341091 A-to-I Human chr15 - 59305370 59305370 59305370 GGCAACATGGCAAAACTCCATCTCTACTAAAAATACAAAAAATTAGCCGGGCATGGTGGTGTGTG GGCAACATGGCAAAACTCCATCTCTACTAAAAGTACAAAAAATTAGCCGGGCATGGTGGTGTGTG T C MYO1E Ensembl:ENSG00000157483 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1471788081 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81330,RMVar_hsa_circ_172490,RMVar_hsa_circ_93592,RMVar_hsa_circ_172500 44269 RMVar_ID_44269 Human_SNP_ID_579348144 A-to-I Human chr15 - 59330942 59330942 59330942 AACGTAGGGAGACTCCATCTCCGCAGATTTTTAAAAAGTTAGCTGGGCGTGATGGTGCATGCCTG AACGTAGGGAGACTCCATCTCCGCAGATTTTTTAAAAGTTAGCTGGGCGTGATGGTGCATGCCTG T A MYO1E Ensembl:ENSG00000157483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs563404972 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81330,RMVar_hsa_circ_172490,RMVar_hsa_circ_93592,RMVar_hsa_circ_172500 44270 RMVar_ID_44270 Human_SNP_ID_579350503 A-to-I Human chr15 - 59339770 59339766 59339770 TTGTCTAGGCTGGTCTTTAACTCCTGGGCTCAAGCAGTCTTCAGGCCTTGGCCGCAAAACTGCTG TTGTCTAGGCTGGTCTTTAACTCCTGGGCTCA____GTCTTCAGGCCTTGGCCGCAAAACTGCTG CTGCT C MYO1E Ensembl:ENSG00000157483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1203647425 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_81330,RMVar_hsa_circ_172490,RMVar_hsa_circ_93592,RMVar_hsa_circ_172500 44271 RMVar_ID_44271 Human_SNP_ID_579350514 A-to-I Human chr15 - 59339803 59339803 59339803 TATAAAATTTTGTAGAGAAGGTATCTCGCTATATTGTCTAGGCTGGTCTTTAACTCCTGGGCTCA TATAAAATTTTGTAGAGAAGGTATCTCGCTATGTTGTCTAGGCTGGTCTTTAACTCCTGGGCTCA T C MYO1E Ensembl:ENSG00000157483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs564540657 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2448366,Human_RBP_ID_12542184 RMVar_hsa_circ_81330,RMVar_hsa_circ_172490,RMVar_hsa_circ_93592,RMVar_hsa_circ_172500 44272 RMVar_ID_44272 Human_SNP_ID_579355863 A-to-I Human chr15 - 59359432 59359432 59359432 CAGGCTGAAGTGCAGTGGTGTGATCTTGTCTCACTGTAGCCTCAACCTCCTAGGCTCAAGAGAGC CAGGCTGAAGTGCAGTGGTGTGATCTTGTCTCGCTGTAGCCTCAACCTCCTAGGCTCAAGAGAGC T C MYO1E,AC092868.3 Ensembl:ENSG00000157483,Ensembl:ENSG00000259735 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1233275614 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81330,RMVar_hsa_circ_172490,RMVar_hsa_circ_93592,RMVar_hsa_circ_172500 44273 RMVar_ID_44273 Human_SNP_ID_579356507 A-to-I Human chr15 - 59361974 59361974 59361974 AAATTAGCCTGGCGTGGTGGTAGACGCCCGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAA AAATTAGCCTGGCGTGGTGGTAGACGCCCGTATTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAA T A MYO1E Ensembl:ENSG00000157483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1180424323 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81330,RMVar_hsa_circ_172490,RMVar_hsa_circ_93592,RMVar_hsa_circ_172500 44274 RMVar_ID_44274 Human_SNP_ID_579357035 A-to-I Human chr15 - 59363861 59363861 59363861 CTGAGGCAGGAGAATCGCTTGAAATGGGAGGCAGAGGTTGTGGTGAACCAAGATCTTGCCACTGC CTGAGGCAGGAGAATCGCTTGAAATGGGAGGCGGAGGTTGTGGTGAACCAAGATCTTGCCACTGC T C MYO1E Ensembl:ENSG00000157483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1428498072 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81330,RMVar_hsa_circ_172490,RMVar_hsa_circ_93592,RMVar_hsa_circ_172500 44275 RMVar_ID_44275 Human_SNP_ID_579357270 A-to-I Human chr15 - 59364783 59364783 59364783 CTCCTGCCTCAACCTCCTGAGTAGCTGGGATTATAGGTACACACTACCATGCCCGGCCAACTGTT CTCCTGCCTCAACCTCCTGAGTAGCTGGGATTGTAGGTACACACTACCATGCCCGGCCAACTGTT T C MYO1E Ensembl:ENSG00000157483 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs762626178 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81330,RMVar_hsa_circ_172490,RMVar_hsa_circ_93592,RMVar_hsa_circ_172500 44276 RMVar_ID_44276 Human_SNP_ID_579383715 A-to-I Human chr15 + 59461521 59461521 59461521 TATAGTATTTTTTGTAGAGACATCGTCTCACTATGTTGCCCAGACAGGGCTTGAACTCCTGGGCT TATAGTATTTTTTGTAGAGACATCGTCTCACTGTGTTGCCCAGACAGGGCTTGAACTCCTGGGCT A G FAM81A Ensembl:ENSG00000157470 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1189230581 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9376,RMVar_hsa_circ_172530,RMVar_hsa_circ_313753 44277 RMVar_ID_44277 Human_SNP_ID_579455575 A-to-I Human chr15 - 59673978 59673978 59673978 TTGAATGATTGTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGTGCACACCACCACACCCA TTGAATGATTGTCCTGCCTCAGCCTCCTGAGTGGCTGGGACTACAGGTGCACACCACCACACCCA T C BNIP2 Ensembl:ENSG00000140299 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1351462342 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56148,RMVar_hsa_circ_350192,RMVar_hsa_circ_21463,RMVar_hsa_circ_172537,RMVar_hsa_circ_341015,RMVar_hsa_circ_359580,RMVar_hsa_circ_314119,RMVar_hsa_circ_18319,RMVar_hsa_circ_303312,RMVar_hsa_circ_268444,RMVar_hsa_circ_172539,RMVar_hsa_circ_299270,RMVar_hsa_circ_172540 44278 RMVar_ID_44278 Human_SNP_ID_579458156 A-to-I Human chr15 - 59681554 59681554 59681554 GTCCCAGCTGCTTAGGAGGCAGAGGCACAAGAATCACCTGAACCCAGGAGGCAGGGGTTGCCGTG GTCCCAGCTGCTTAGGAGGCAGAGGCACAAGAGTCACCTGAACCCAGGAGGCAGGGGTTGCCGTG T C BNIP2 Ensembl:ENSG00000140299 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs977165656 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21463,RMVar_hsa_circ_314119,RMVar_hsa_circ_18319,RMVar_hsa_circ_309596,RMVar_hsa_circ_172541 44279 RMVar_ID_44279 Human_SNP_ID_579458160 A-to-I Human chr15 - 59681566 59681566 59681566 CGCTCGCCTGTAGTCCCAGCTGCTTAGGAGGCAGAGGCACAAGAATCACCTGAACCCAGGAGGCA CGCTCGCCTGTAGTCCCAGCTGCTTAGGAGGCGGAGGCACAAGAATCACCTGAACCCAGGAGGCA T C BNIP2 Ensembl:ENSG00000140299 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs539819023 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21463,RMVar_hsa_circ_314119,RMVar_hsa_circ_18319,RMVar_hsa_circ_309596,RMVar_hsa_circ_172541 44280 RMVar_ID_44280 Human_SNP_ID_579458178 A-to-I Human chr15 - 59681610 59681610 59681610 AAACCCCGTCTCTACTAAAAATACAAAAAATTAGCCAGGCTTGGCGCTCGCCTGTAGTCCCAGCT AAACCCCGTCTCTACTAAAAATACAAAAAATTCGCCAGGCTTGGCGCTCGCCTGTAGTCCCAGCT T G BNIP2 Ensembl:ENSG00000140299 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1049129430 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21463,RMVar_hsa_circ_314119,RMVar_hsa_circ_18319,RMVar_hsa_circ_309596,RMVar_hsa_circ_172541 44281 RMVar_ID_44281 Human_SNP_ID_579458194 A-to-I Human chr15 - 59681648 59681648 59681648 GAGGCCAGGAGTTTGAGACCAACGTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAA GAGGCCAGGAGTTTGAGACCAACGTGGCCAACGTGGTGAAACCCCGTCTCTACTAAAAATACAAA T C BNIP2 Ensembl:ENSG00000140299 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1406041649 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21463,RMVar_hsa_circ_314119,RMVar_hsa_circ_18319,RMVar_hsa_circ_309596,RMVar_hsa_circ_172541 44282 RMVar_ID_44282 Human_SNP_ID_579458202 A-to-I Human chr15 - 59681659 59681659 59681659 GCAGATCACTTGAGGCCAGGAGTTTGAGACCAACGTGGCCAACATGGTGAAACCCCGTCTCTACT GCAGATCACTTGAGGCCAGGAGTTTGAGACCAGCGTGGCCAACATGGTGAAACCCCGTCTCTACT T C BNIP2 Ensembl:ENSG00000140299 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs899720607 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21463,RMVar_hsa_circ_314119,RMVar_hsa_circ_18319,RMVar_hsa_circ_309596,RMVar_hsa_circ_172541 44283 RMVar_ID_44283 Human_SNP_ID_579458203 A-to-I Human chr15 - 59681659 59681659 59681659 GCAGATCACTTGAGGCCAGGAGTTTGAGACCAACGTGGCCAACATGGTGAAACCCCGTCTCTACT GCAGATCACTTGAGGCCAGGAGTTTGAGACCACCGTGGCCAACATGGTGAAACCCCGTCTCTACT T G BNIP2 Ensembl:ENSG00000140299 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs899720607 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21463,RMVar_hsa_circ_314119,RMVar_hsa_circ_18319,RMVar_hsa_circ_309596,RMVar_hsa_circ_172541 44284 RMVar_ID_44284 Human_SNP_ID_347533020 A-to-I Human chr8 - 299729 299729 299729 TGAAGCACGGTTTGATTTTCTCTCTCCCCCTCACCATCCCCAGATTTTAGTTGTGACTATCTCCA TGAAGCACGGTTTGATTTTCTCTCTCCCCCTCGCCATCCCCAGATTTTAGTTGTGACTATCTCCA T C HSALNG0062869 RNACentral:URS0000E98AAD lincRNA exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1270756852 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18116105 44285 RMVar_ID_44285 Human_SNP_ID_347662770 A-to-I Human chr8 - 638386 638386 638386 CACCGCACTGTAACGGAAGCTGTATCTCAAGCAGGCCTCCTCTCCGAAGAACATGGCCCGTGCTG CACCGCACTGTAACGGAAGCTGTATCTCAAGCTGGCCTCCTCTCCGAAGAACATGGCCCGTGCTG T A ERICH1 Ensembl:ENSG00000104714 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs543249262 Functional Loss SNV dbSNP153 33..33 33 - - - 44286 RMVar_ID_44286 Human_SNP_ID_347662771 A-to-I Human chr8 - 638386 638386 638386 CACCGCACTGTAACGGAAGCTGTATCTCAAGCAGGCCTCCTCTCCGAAGAACATGGCCCGTGCTG CACCGCACTGTAACGGAAGCTGTATCTCAAGCGGGCCTCCTCTCCGAAGAACATGGCCCGTGCTG T C ERICH1 Ensembl:ENSG00000104714 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs543249262 Functional Loss SNV dbSNP153 33..33 33 - - - 44287 RMVar_ID_44287 Human_SNP_ID_347925451 A-to-I Human chr8 + 1305982 1305982 1305982 GGGAACAACTACTAATTTTTGCATGTAATTTTATATCCAGATATTTTGCTGAATTCCTTTTTCAG GGGAACAACTACTAATTTTTGCATGTAATTTTGTATCCAGATATTTTGCTGAATTCCTTTTTCAG A G DLGAP2 Ensembl:ENSG00000198010 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1303826307 Functional Loss SNV dbSNP153 33..33 33 - - - 44288 RMVar_ID_44288 Human_SNP_ID_347925452 A-to-I Human chr8 + 1305982 1305982 1305982 GGGAACAACTACTAATTTTTGCATGTAATTTTATATCCAGATATTTTGCTGAATTCCTTTTTCAG GGGAACAACTACTAATTTTTGCATGTAATTTTTTATCCAGATATTTTGCTGAATTCCTTTTTCAG A T DLGAP2 Ensembl:ENSG00000198010 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1303826307 Functional Loss SNV dbSNP153 33..33 33 - - - 44289 RMVar_ID_44289 Human_SNP_ID_347926655 A-to-I Human chr8 + 1308777 1308777 1308777 GAACTCCCGACCTCGGATGATCTGCCCGCCTCAGCCTCCCCAAGTGCTGGGATTACAGGCATGAG GAACTCCCGACCTCGGATGATCTGCCCGCCTCGGCCTCCCCAAGTGCTGGGATTACAGGCATGAG A G DLGAP2 Ensembl:ENSG00000198010 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1337062537 Functional Loss SNV dbSNP153 33..33 33 - - - 44290 RMVar_ID_44290 Human_SNP_ID_348118295 A-to-I Human chr8 + 1781093 1781093 1781093 TATGAAATTCTAAGCTGGGTGGGGTGGCTCACACCCGACGTAATCCCAGCACGTTGGGAGGCCGA TATGAAATTCTAAGCTGGGTGGGGTGGCTCACGCCCGACGTAATCCCAGCACGTTGGGAGGCCGA A G CLN8,AC019257.8 Ensembl:ENSG00000182372,Ensembl:ENSG00000283239 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1210556711 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1054866,Human_RBP_ID_18114889 44291 RMVar_ID_44291 Human_SNP_ID_348118351 A-to-I Human chr8 + 1781237 1781237 1781237 AAAATTAGCCGGGTGTCGTGGCACACACCTGTAATCCCAGCTATTTGGGAGGCCAAGGCAGGAGA AAAATTAGCCGGGTGTCGTGGCACACACCTGTGATCCCAGCTATTTGGGAGGCCAAGGCAGGAGA A G CLN8,AC019257.8 Ensembl:ENSG00000182372,Ensembl:ENSG00000283239 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1313432167 Functional Loss SNV dbSNP153 33..33 33 - - - 44292 RMVar_ID_44292 Human_SNP_ID_348118816 A-to-I Human chr8 + 1782406 1782406 1782406 ACTAAAAGTGATCTGCCCACCTCGGCCTCCCAAAGTTCTGGGATTACGGGCGTGAGCCACTTCAC ACTAAAAGTGATCTGCCCACCTCGGCCTCCCAGAGTTCTGGGATTACGGGCGTGAGCCACTTCAC A G CLN8,AC019257.8 Ensembl:ENSG00000182372,Ensembl:ENSG00000283239 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1563115941 Functional Loss SNV dbSNP153 33..33 33 - - - 44293 RMVar_ID_44293 Human_SNP_ID_348193160 A-to-I Human chr8 - 1969956 1969956 1969956 TGGTCCCAGCACTTTGGGAGGCTGAGGCGGGCAGATTGCCTGAGCCTAGGAGTTGGAGACCAGCC TGGTCCCAGCACTTTGGGAGGCTGAGGCGGGCGGATTGCCTGAGCCTAGGAGTTGGAGACCAGCC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs546467314 Functional Loss SNV dbSNP153 33..33 33 - - - 44294 RMVar_ID_44294 Human_SNP_ID_348268710 A-to-I Human chr8 + 2157078 2157078 2157078 CACCATGCCCGGCTAGTTCTTGTATTTTTGGTAAAGATAGGGTTTCACTATGTTTCCCAGGCTGG CACCATGCCCGGCTAGTTCTTGTATTTTTGGTGAAGATAGGGTTTCACTATGTTTCCCAGGCTGG A G MYOM2 Ensembl:ENSG00000036448 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251399622 Functional Loss SNV dbSNP153 33..33 33 - - - 44295 RMVar_ID_44295 Human_SNP_ID_348268711 A-to-I Human chr8 + 2157078 2157078 2157078 CACCATGCCCGGCTAGTTCTTGTATTTTTGGTAAAGATAGGGTTTCACTATGTTTCCCAGGCTGG CACCATGCCCGGCTAGTTCTTGTATTTTTGGTTAAGATAGGGTTTCACTATGTTTCCCAGGCTGG A T MYOM2 Ensembl:ENSG00000036448 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251399622 Functional Loss SNV dbSNP153 33..33 33 - - - 44296 RMVar_ID_44296 Human_SNP_ID_348370563 A-to-I Human chr8 - 2532570 2532570 2532570 GGGCTTGGTGGCGGGCATCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCATGAA GGGCTTGGTGGCGGGCATCTGTAGTCCCAGCTCCTCGGGAGGCTGAGGCAGGAGAATGGCATGAA T G AC245187.2 Ensembl:ENSG00000282142 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs995270858 Functional Loss SNV dbSNP153 33..33 33 - - - 44297 RMVar_ID_44297 Human_SNP_ID_348370565 A-to-I Human chr8 - 2532574 2532574 2532574 AGCCGGGCTTGGTGGCGGGCATCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCA AGCCGGGCTTGGTGGCGGGCATCTGTAGTCCCGGCTACTCGGGAGGCTGAGGCAGGAGAATGGCA T C AC245187.2 Ensembl:ENSG00000282142 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277218222 Functional Loss SNV dbSNP153 33..33 33 - - - 44298 RMVar_ID_44298 Human_SNP_ID_348370566 A-to-I Human chr8 - 2532574 2532574 2532574 AGCCGGGCTTGGTGGCGGGCATCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCA AGCCGGGCTTGGTGGCGGGCATCTGTAGTCCCCGCTACTCGGGAGGCTGAGGCAGGAGAATGGCA T G AC245187.2 Ensembl:ENSG00000282142 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277218222 Functional Loss SNV dbSNP153 33..33 33 - - - 44299 RMVar_ID_44299 Human_SNP_ID_349031530 A-to-I Human chr8 - 3927517 3927517 3927517 GGGATTACAGTGATGCACCACCACGGCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTCTCA GGGATTACAGTGATGCACCACCACGGCTGGCTGATTTTTGTATTTTTAGTAGAGATGGGGTCTCA T C CSMD1 Ensembl:ENSG00000183117 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs943738461 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10505,RMVar_hsa_circ_290399,RMVar_hsa_circ_40762,RMVar_hsa_circ_19283,RMVar_hsa_circ_28760,RMVar_hsa_circ_10847,RMVar_hsa_circ_36488,RMVar_hsa_circ_28032,RMVar_hsa_circ_250069,RMVar_hsa_circ_250071,RMVar_hsa_circ_296883,RMVar_hsa_circ_250070,RMVar_hsa_circ_250072 44300 RMVar_ID_44300 Human_SNP_ID_349295117 A-to-I Human chr8 - 4334015 4334015 4334015 GTTGTGGTGGGTGCCTGTGGTCCCAGGTACTCAGGAGTCTGAGGCGGGAGGATGGCTTGAGGCAG GTTGTGGTGGGTGCCTGTGGTCCCAGGTACTCTGGAGTCTGAGGCGGGAGGATGGCTTGAGGCAG T A CSMD1 Ensembl:ENSG00000183117 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1045580312 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10505,RMVar_hsa_circ_36488 44301 RMVar_ID_44301 Human_SNP_ID_349295213 A-to-I Human chr8 - 4334152 4334152 4334152 CTGTAATCCCAGCACTTTGGGAAGCTGAGGCCAGAGGATATCTTGAGTTCGGGAGTTTGAGACCA CTGTAATCCCAGCACTTTGGGAAGCTGAGGCCGGAGGATATCTTGAGTTCGGGAGTTTGAGACCA T C CSMD1 Ensembl:ENSG00000183117 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1047728863 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10505,RMVar_hsa_circ_36488 44302 RMVar_ID_44302 Human_SNP_ID_349308529 A-to-I Human chr8 - 4356410 4356410 4356410 TGTACATGCATGTTTATAGTAGCACAATTGACAATTGCAAAATCGTAGAACCAACCCAAATGTCC TGTACATGCATGTTTATAGTAGCACAATTGACCATTGCAAAATCGTAGAACCAACCCAAATGTCC T G CSMD1 Ensembl:ENSG00000183117 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1393972606 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10505,RMVar_hsa_circ_36488 44303 RMVar_ID_44303 Human_SNP_ID_349311892 A-to-I Human chr8 - 4361845 4361845 4361845 GTTCAAGCAATTCTTCTGCCTTAGCCTCCCAAATAGCTGGGAGTACAGGCGCCCCGCACCACGCC GTTCAAGCAATTCTTCTGCCTTAGCCTCCCAAGTAGCTGGGAGTACAGGCGCCCCGCACCACGCC T C CSMD1 Ensembl:ENSG00000183117 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1199189186 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10505,RMVar_hsa_circ_36488 44304 RMVar_ID_44304 Human_SNP_ID_349415356 A-to-I Human chr8 - 4541565 4541565 4541565 TTTTGCATTTTTAGTACAGACAGGGTTTTACCATGGTGGCCAGGCTGTTCTTGAACTCCTGACCT TTTTGCATTTTTAGTACAGACAGGGTTTTACCGTGGTGGCCAGGCTGTTCTTGAACTCCTGACCT T C CSMD1 Ensembl:ENSG00000183117 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1022868703 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36488,RMVar_hsa_circ_298345 44305 RMVar_ID_44305 Human_SNP_ID_349433764 A-to-I Human chr8 - 4579577 4579577 4579577 TTGGTGGATCATGAGGTGAGGATCTCGAGACCAGCCTGGCTAACATGCTGAGACCCCATCTCTAC TTGGTGGATCATGAGGTGAGGATCTCGAGACCGGCCTGGCTAACATGCTGAGACCCCATCTCTAC T C CSMD1 Ensembl:ENSG00000183117 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1294039563 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36488,RMVar_hsa_circ_298345,RMVar_hsa_circ_250079 44306 RMVar_ID_44306 Human_SNP_ID_349448711 A-to-I Human chr8 - 4609315 4609315 4609315 CTCACTACAACCTCTGCCTCCCAGGCTCCAGCAATCCTCCCACCTCAGCCTCCTGAGTAGCTGGG CTCACTACAACCTCTGCCTCCCAGGCTCCAGCTATCCTCCCACCTCAGCCTCCTGAGTAGCTGGG T A CSMD1 Ensembl:ENSG00000183117 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs566690720 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36488,RMVar_hsa_circ_298345,RMVar_hsa_circ_250079 44307 RMVar_ID_44307 Human_SNP_ID_349448712 A-to-I Human chr8 - 4609315 4609315 4609315 CTCACTACAACCTCTGCCTCCCAGGCTCCAGCAATCCTCCCACCTCAGCCTCCTGAGTAGCTGGG CTCACTACAACCTCTGCCTCCCAGGCTCCAGCCATCCTCCCACCTCAGCCTCCTGAGTAGCTGGG T G CSMD1 Ensembl:ENSG00000183117 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs566690720 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36488,RMVar_hsa_circ_298345,RMVar_hsa_circ_250079 44308 RMVar_ID_44308 Human_SNP_ID_349553363 A-to-I Human chr8 - 4814426 4814426 4814426 CTTGGCCAACATGGTGAAACCGTGTTTCTACTAAAAATAACAAAAATTAGCCAGGCTTGGCGGTG CTTGGCCAACATGGTGAAACCGTGTTTCTACTGAAAATAACAAAAATTAGCCAGGCTTGGCGGTG T C CSMD1 Ensembl:ENSG00000183117 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs957077851 Functional Loss SNV dbSNP153 33..33 33 - - - 44309 RMVar_ID_44309 Human_SNP_ID_349572440 A-to-I Human chr8 - 4851004 4851004 4851004 ACCAACATGGCACATGTATACATATGTAACTAACCTGCACTTTGTGCACATGTACCCTAAAACTC ACCAACATGGCACATGTATACATATGTAACTAGCCTGCACTTTGTGCACATGTACCCTAAAACTC T C CSMD1 Ensembl:ENSG00000183117 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs933676983 Functional Loss SNV dbSNP153 33..33 33 - - - 44310 RMVar_ID_44310 Human_SNP_ID_349572447 A-to-I Human chr8 - 4851032 4851032 4851032 CTAAATGATGTGTTAATGGGTGCAGCACACCAACATGGCACATGTATACATATGTAACTAACCTG CTAAATGATGTGTTAATGGGTGCAGCACACCAGCATGGCACATGTATACATATGTAACTAACCTG T C CSMD1 Ensembl:ENSG00000183117 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1563585832 Functional Loss SNV dbSNP153 33..33 33 - - - 44311 RMVar_ID_44311 Human_SNP_ID_349584825 A-to-I Human chr8 - 4877467 4877467 4877467 GAGATTTTAGGAGCTACTTTGAAATAGCAAATATGACTTTATAACATCTGGTGTTTATAAGGGAC GAGATTTTAGGAGCTACTTTGAAATAGCAAATGTGACTTTATAACATCTGGTGTTTATAAGGGAC T C CSMD1 Ensembl:ENSG00000183117 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1321248239 Functional Loss SNV dbSNP153 33..33 33 - - - 44312 RMVar_ID_44312 Human_SNP_ID_349600287 A-to-I Human chr8 - 4907766 4907766 4907766 AGCCCAGGGGTTTCGGAGCAGCCTGGGAAACAAAGCAAGACCCCATCTCTACAAAAAATGAAAAA AGCCCAGGGGTTTCGGAGCAGCCTGGGAAACAGAGCAAGACCCCATCTCTACAAAAAATGAAAAA T C CSMD1 Ensembl:ENSG00000183117 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1423793110 Functional Loss SNV dbSNP153 33..33 33 - - - 44313 RMVar_ID_44313 Human_SNP_ID_349618825 A-to-I Human chr8 - 4941727 4941727 4941727 GGGCATAATGGCACATGCCTGTGGTCCCAACTACTCAGGAGGTTGAGGCGAGAGAATTGCTTGAG GGGCATAATGGCACATGCCTGTGGTCCCAACTGCTCAGGAGGTTGAGGCGAGAGAATTGCTTGAG T C CSMD1 Ensembl:ENSG00000183117 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1303725406 Functional Loss SNV dbSNP153 33..33 33 - - - 44314 RMVar_ID_44314 Human_SNP_ID_349618896 A-to-I Human chr8 - 4941826 4941826 4941826 GTAGGCTGAGGTGGGAGGATTGCTTTGAGCTCAGGAGTTCAAGACCATCCTGGGCAACATGGGGA GTAGGCTGAGGTGGGAGGATTGCTTTGAGCTCGGGAGTTCAAGACCATCCTGGGCAACATGGGGA T C CSMD1 Ensembl:ENSG00000183117 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs906507215 Functional Loss SNV dbSNP153 33..33 33 - - - 44315 RMVar_ID_44315 Human_SNP_ID_349630654 A-to-I Human chr8 - 4964347 4964347 4964347 ACCCGGCTTATTTTTTTTCTTGTACTTTTTGTAGAAATGGGATTTTGCCATGCTGCCCTGCTGGT ACCCGGCTTATTTTTTTTCTTGTACTTTTTGTGGAAATGGGATTTTGCCATGCTGCCCTGCTGGT T C CSMD1 Ensembl:ENSG00000183117 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1360377189 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_250081 44316 RMVar_ID_44316 Human_SNP_ID_350298802 A-to-I Human chr8 - 6401137 6401137 6401137 GCTTGCCCTCTGGACTTAAAAAAACTGGGTTTATATTCTGCTCTGAACATTAATCATTGTTTTTA GCTTGCCCTCTGGACTTAAAAAAACTGGGTTTGTATTCTGCTCTGAACATTAATCATTGTTTTTA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs777284191 Functional Loss SNV dbSNP153 33..33 33 - - - 44317 RMVar_ID_44317 Human_SNP_ID_350298803 A-to-I Human chr8 - 6401137 6401137 6401137 GCTTGCCCTCTGGACTTAAAAAAACTGGGTTTATATTCTGCTCTGAACATTAATCATTGTTTTTA GCTTGCCCTCTGGACTTAAAAAAACTGGGTTTCTATTCTGCTCTGAACATTAATCATTGTTTTTA T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs777284191 Functional Loss SNV dbSNP153 33..33 33 - - - 44318 RMVar_ID_44318 Human_SNP_ID_350300026 A-to-I Human chr8 - 6403976 6403976 6403976 TTTTAAATTCTTTGTAGAGGCGGAGTCCCACTATGTTGCCCAGGCTGGTCTTGAACTCCTGGGCT TTTTAAATTCTTTGTAGAGGCGGAGTCCCACTGTGTTGCCCAGGCTGGTCTTGAACTCCTGGGCT T C AC016065.1 Ensembl:ENSG00000246089 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs776510240 Functional Loss SNV dbSNP153 33..33 33 - - - 44319 RMVar_ID_44319 Human_SNP_ID_350322101 A-to-I Human chr8 + 6457498 6457498 6457498 CTGGTGGTGGGCACCTGTAATCCCAGCTGCTCAAGAGACTGAGGTGGGAGAATCACCTGAACCCA CTGGTGGTGGGCACCTGTAATCCCAGCTGCTCCAGAGACTGAGGTGGGAGAATCACCTGAACCCA A C MCPH1 Ensembl:ENSG00000147316 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1165247639 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76828,RMVar_hsa_circ_21793,RMVar_hsa_circ_250086,RMVar_hsa_circ_97797,RMVar_hsa_circ_265021,RMVar_hsa_circ_88472,RMVar_hsa_circ_105556,RMVar_hsa_circ_250088,RMVar_hsa_circ_109222,RMVar_hsa_circ_250089,RMVar_hsa_circ_250091,RMVar_hsa_circ_50580,RMVar_hsa_circ_351252,RMVar_hsa_circ_250090,RMVar_hsa_circ_322873 44320 RMVar_ID_44320 Human_SNP_ID_350326482 A-to-I Human chr8 + 6469081 6469081 6469081 TAGTTGGACATGATGGTGGCCACCTGTGGTCCAAGCTACTAGGGAGGCTTGAGACCAGGAATTCG TAGTTGGACATGATGGTGGCCACCTGTGGTCCCAGCTACTAGGGAGGCTTGAGACCAGGAATTCG A C MCPH1 Ensembl:ENSG00000147316 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs60525187 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76828,RMVar_hsa_circ_21793,RMVar_hsa_circ_250086,RMVar_hsa_circ_97797,RMVar_hsa_circ_265021,RMVar_hsa_circ_88472,RMVar_hsa_circ_105556,RMVar_hsa_circ_250088,RMVar_hsa_circ_109222,RMVar_hsa_circ_250089,RMVar_hsa_circ_250091,RMVar_hsa_circ_50580,RMVar_hsa_circ_351252,RMVar_hsa_circ_250090,RMVar_hsa_circ_322873 44321 RMVar_ID_44321 Human_SNP_ID_350392497 A-to-I Human chr8 + 6643445 6643445 6643445 TGCCACCATGCCTGGCTAATTTTTGTAGTTTTAGTAGAGACAGGGTTTCGCCATGTTGGCCAGGC TGCCACCATGCCTGGCTAATTTTTGTAGTTTTGGTAGAGACAGGGTTTCGCCATGTTGGCCAGGC A G MCPH1 Ensembl:ENSG00000147316 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1019884139 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_179189 RMVar_hsa_circ_88472,RMVar_hsa_circ_105556,RMVar_hsa_circ_250089,RMVar_hsa_circ_250091 44322 RMVar_ID_44322 Human_SNP_ID_350392507 A-to-I Human chr8 + 6643465 6643465 6643465 TTTTGTAGTTTTAGTAGAGACAGGGTTTCGCCATGTTGGCCAGGCTGGTCTCAAACGCCTGAGCT TTTTGTAGTTTTAGTAGAGACAGGGTTTCGCCGTGTTGGCCAGGCTGGTCTCAAACGCCTGAGCT A G MCPH1 Ensembl:ENSG00000147316 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs527964849 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88472,RMVar_hsa_circ_105556,RMVar_hsa_circ_250089,RMVar_hsa_circ_250091 44323 RMVar_ID_44323 Human_SNP_ID_350392761 A-to-I Human chr8 + 6644182 6644182 6644182 TGAGGCAGAAGAATCGCTTGAACCCAAGAGGCAGAGGTTGCAGTGAGCCAAGGTTGCAGTGAATC TGAGGCAGAAGAATCGCTTGAACCCAAGAGGCCGAGGTTGCAGTGAGCCAAGGTTGCAGTGAATC A C MCPH1 Ensembl:ENSG00000147316 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs113613187 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5034,GWAS_ID_5035 44324 RMVar_ID_44324 Human_SNP_ID_350392762 A-to-I Human chr8 + 6644182 6644182 6644182 TGAGGCAGAAGAATCGCTTGAACCCAAGAGGCAGAGGTTGCAGTGAGCCAAGGTTGCAGTGAATC TGAGGCAGAAGAATCGCTTGAACCCAAGAGGCGGAGGTTGCAGTGAGCCAAGGTTGCAGTGAATC A G MCPH1 Ensembl:ENSG00000147316 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs113613187 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5034,GWAS_ID_5035 44325 RMVar_ID_44325 Human_SNP_ID_350412324 A-to-I Human chr8 - 6695613 6695613 6695613 TCGCCCAGGCTGGAGTGCAGTGGCAAGATCTCAGCTCACTGCAAGCTCCGCCTCCCAGGTTCACA TCGCCCAGGCTGGAGTGCAGTGGCAAGATCTCGGCTCACTGCAAGCTCCGCCTCCCAGGTTCACA T C MCPH1-AS1 Ensembl:ENSG00000249898 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1423650492 Functional Loss SNV dbSNP153 33..33 33 - - - 44326 RMVar_ID_44326 Human_SNP_ID_350419969 A-to-I Human chr8 + 6713683 6713683 6713683 TCAAGCGGTCCTCCCACCTCAGCCTCCTGAGTAGCTGGGACTACAGGTACACAGCACCATGCCCA TCAAGCGGTCCTCCCACCTCAGCCTCCTGAGTGGCTGGGACTACAGGTACACAGCACCATGCCCA A G AGPAT5 Ensembl:ENSG00000155189 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1298715989 Functional Loss SNV dbSNP153 33..33 33 - - - 44327 RMVar_ID_44327 Human_SNP_ID_350875106 A-to-I Human chr8 - 8234960 8234960 8234960 TTTTGTATTTTTAGTAGAGACACGGTTTCACCATATTGGCCAGGCTGGTCTCGAACTTCTGACCT TTTTGTATTTTTAGTAGAGACACGGTTTCACCGTATTGGCCAGGCTGGTCTCGAACTTCTGACCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1192384101 Functional Loss SNV dbSNP153 33..33 33 - - - 44328 RMVar_ID_44328 Human_SNP_ID_350875231 A-to-I Human chr8 - 8235297 8235297 8235297 CGACTACAGGCATGCGCCACCATGTCCGGCTAATTTTTGTACTTTTTTTTGAGACAGAGTTTCGT CGACTACAGGCATGCGCCACCATGTCCGGCTAGTTTTTGTACTTTTTTTTGAGACAGAGTTTCGT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1424325237 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16479096 44329 RMVar_ID_44329 Human_SNP_ID_350875262 A-to-I Human chr8 - 8235377 8235377 8235377 CAGTGGCACGATCTTGGCTCACTGCAACCTCCACCTCCTGGGTTCAAGCAATTCTCCTGCCTCAG CAGTGGCACGATCTTGGCTCACTGCAACCTCCGCCTCCTGGGTTCAAGCAATTCTCCTGCCTCAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335812752 Functional Loss SNV dbSNP153 33..33 33 - - - 44330 RMVar_ID_44330 Human_SNP_ID_350875263 A-to-I Human chr8 - 8235377 8235377 8235377 CAGTGGCACGATCTTGGCTCACTGCAACCTCCACCTCCTGGGTTCAAGCAATTCTCCTGCCTCAG CAGTGGCACGATCTTGGCTCACTGCAACCTCCCCCTCCTGGGTTCAAGCAATTCTCCTGCCTCAG T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335812752 Functional Loss SNV dbSNP153 33..33 33 - - - 44331 RMVar_ID_44331 Human_SNP_ID_350921505 A-to-I Human chr8 - 8366451 8366451 8366451 AAATTAGCCAGACATTGTGGCAGACGCATGTAATCTTAGCTACTCAGGAGGCTGAGGCAGAAGAA AAATTAGCCAGACATTGTGGCAGACGCATGTATTCTTAGCTACTCAGGAGGCTGAGGCAGAAGAA T A PRAG1 Ensembl:ENSG00000275342 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1213438564 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_346666 44332 RMVar_ID_44332 Human_SNP_ID_350921613 A-to-I Human chr8 - 8366806 8366806 8366806 GGGCATGGTGGCACATACCTGTAGTTACAGCTACTTGGGAGGCTGATGTGGGAGGATTGCTTGAG GGGCATGGTGGCACATACCTGTAGTTACAGCTGCTTGGGAGGCTGATGTGGGAGGATTGCTTGAG T C PRAG1 Ensembl:ENSG00000275342 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1306294923 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17578538 RMVar_hsa_circ_346666 44333 RMVar_ID_44333 Human_SNP_ID_351150623 A-to-I Human chr8 + 9004544 9004544 9004544 ACAAAAAGCCGGTCGTAGTTGCCCTCTCCCGTAGTCCCAGCTACTGGGGAGGCTCAGTGGGGAGG ACAAAAAGCCGGTCGTAGTTGCCCTCTCCCGTTGTCCCAGCTACTGGGGAGGCTCAGTGGGGAGG A T ERI1 Ensembl:ENSG00000104626 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1382641937 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28865 44334 RMVar_ID_44334 Human_SNP_ID_351425043 A-to-I Human chr8 + 9782012 9782012 9782012 TTTGGCATATATTTACAGTAAAAGCATTCATTATTTGTCTGAAATTCAAATTTAACTGAGCATGC TTTGGCATATATTTACAGTAAAAGCATTCATTGTTTGTCTGAAATTCAAATTTAACTGAGCATGC A G TNKS Ensembl:ENSG00000173273 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs10191 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_706307,Human_RBP_ID_5003025,Human_RBP_ID_26557987 RMVar_hsa_circ_95985,RMVar_hsa_circ_250127,RMVar_hsa_circ_268530 44335 RMVar_ID_44335 Human_SNP_ID_351472252 A-to-I Human chr8 - 9900984 9900984 9900984 CCCTTCTGTGCTCAAATGAGGTGTCCGAGTGAAGGTCAGCCCTTCCCTTCTGTATTTGGGGCCTA CCCTTCTGTGCTCAAATGAGGTGTCCGAGTGAGGGTCAGCCCTTCCCTTCTGTATTTGGGGCCTA T C LINC00599 Ensembl:ENSG00000253230 lincRNA exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs757276711 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_250166,RMVar_hsa_circ_250165,RMVar_hsa_circ_269153 44336 RMVar_ID_44336 Human_SNP_ID_351596640 A-to-I Human chr8 + 10242022 10242022 10242022 AGCCGGATGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCGGAGGGGGGCAGATCACC AGCCGGATGTGGTGGCTCACGCCTGTAATCCCGGCACTTTGGGAGGCGGAGGGGGGCAGATCACC A G MSRA Ensembl:ENSG00000175806 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1373699117 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47459,RMVar_hsa_circ_303465,RMVar_hsa_circ_250178,RMVar_hsa_circ_250177,RMVar_hsa_circ_295214,RMVar_hsa_circ_312430,RMVar_hsa_circ_293489,RMVar_hsa_circ_250175,RMVar_hsa_circ_250176,RMVar_hsa_circ_250174 44337 RMVar_ID_44337 Human_SNP_ID_351635618 A-to-I Human chr8 + 10344427 10344427 10344427 GAAACCCCGTCTCTACTAAAAATACAAAAATTAGACAGGCGTGGTGGTGGGCTCCTGAAGTCCCA GAAACCCCGTCTCTACTAAAAATACAAAAATTTGACAGGCGTGGTGGTGGGCTCCTGAAGTCCCA A T MSRA Ensembl:ENSG00000175806 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1403641169 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_250187 44338 RMVar_ID_44338 Human_SNP_ID_351668755 A-to-I Human chr8 + 10431709 10431709 10431709 CACCCACCTCGGCCTCCCAAAGTTTTAGGATTACTGGTGTGAGCCACTGCACCCGGCAAGGGTGC CACCCACCTCGGCCTCCCAAAGTTTTAGGATTGCTGGTGTGAGCCACTGCACCCGGCAAGGGTGC A G - - Other Unknown GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1479596287 Functional Loss SNV dbSNP153 33..33 33 - - - 44339 RMVar_ID_44339 Human_SNP_ID_351673837 A-to-I Human chr8 + 10444984 10444984 10444984 AGAATTTCACTCTATCACCCAGGCTGCAGTACAGTGGCACAATCTTGGCTCACTGCAACCTCTGC AGAATTTCACTCTATCACCCAGGCTGCAGTACCGTGGCACAATCTTGGCTCACTGCAACCTCTGC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs7459635 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_250193,RMVar_hsa_circ_250192 44340 RMVar_ID_44340 Human_SNP_ID_351673838 A-to-I Human chr8 + 10444984 10444984 10444984 AGAATTTCACTCTATCACCCAGGCTGCAGTACAGTGGCACAATCTTGGCTCACTGCAACCTCTGC AGAATTTCACTCTATCACCCAGGCTGCAGTACGGTGGCACAATCTTGGCTCACTGCAACCTCTGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs7459635 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_250193,RMVar_hsa_circ_250192 44341 RMVar_ID_44341 Human_SNP_ID_351673839 A-to-I Human chr8 + 10444984 10444984 10444984 AGAATTTCACTCTATCACCCAGGCTGCAGTACAGTGGCACAATCTTGGCTCACTGCAACCTCTGC AGAATTTCACTCTATCACCCAGGCTGCAGTACTGTGGCACAATCTTGGCTCACTGCAACCTCTGC A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs7459635 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_250193,RMVar_hsa_circ_250192 44342 RMVar_ID_44342 Human_SNP_ID_351676282 A-to-I Human chr8 + 10451299 10451299 10451299 TCTCTTCCATTGGTCTATATCTCTGTTTCGGTACCAGTACCATGCTGTTTTGGTTACTGTAGCCT TCTCTTCCATTGGTCTATATCTCTGTTTCGGTGCCAGTACCATGCTGTTTTGGTTACTGTAGCCT A G - - Other Unknown GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1039720805 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_250193,RMVar_hsa_circ_250192 44343 RMVar_ID_44343 Human_SNP_ID_351881138 A-to-I Human chr8 - 11009254 11009254 11009254 TGCTCACCTTGGCCTCCCAAATTGCTGGGATTACAGGTGTGAGTCACCATGCCCGGCCAAACCCT TGCTCACCTTGGCCTCCCAAATTGCTGGGATTGCAGGTGTGAGTCACCATGCCCGGCCAAACCCT T C XKR6 Ensembl:ENSG00000171044 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1047211193 Functional Loss SNV dbSNP153 33..33 33 - - - 44344 RMVar_ID_44344 Human_SNP_ID_351881139 A-to-I Human chr8 - 11009254 11009254 11009254 TGCTCACCTTGGCCTCCCAAATTGCTGGGATTACAGGTGTGAGTCACCATGCCCGGCCAAACCCT TGCTCACCTTGGCCTCCCAAATTGCTGGGATTCCAGGTGTGAGTCACCATGCCCGGCCAAACCCT T G XKR6 Ensembl:ENSG00000171044 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1047211193 Functional Loss SNV dbSNP153 33..33 33 - - - 44345 RMVar_ID_44345 Human_SNP_ID_351881142 A-to-I Human chr8 - 11009266 11009266 11009266 GCTCAAGCAATCTGCTCACCTTGGCCTCCCAAATTGCTGGGATTACAGGTGTGAGTCACCATGCC GCTCAAGCAATCTGCTCACCTTGGCCTCCCAAGTTGCTGGGATTACAGGTGTGAGTCACCATGCC T C XKR6 Ensembl:ENSG00000171044 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1313146359 Functional Loss SNV dbSNP153 33..33 33 - - - 44346 RMVar_ID_44346 Human_SNP_ID_351904621 A-to-I Human chr8 - 11081802 11081802 11081802 CCAGGGAAACAGTGGAAATTCCACTGATTCCTAATGAACACTTGCAGAATAAGCCTCTGACTGAC CCAGGGAAACAGTGGAAATTCCACTGATTCCTTATGAACACTTGCAGAATAAGCCTCTGACTGAC T A XKR6 Ensembl:ENSG00000171044 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1332780270 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_250207 44347 RMVar_ID_44347 Human_SNP_ID_351913800 A-to-I Human chr8 - 11106619 11106619 11106619 ATCTTGAACTCCTGACCTCAAGTGATCTGCCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGC ATCTTGAACTCCTGACCTCAAGTGATCTGCCCTCCTCAGCCTCCCAAAGTGCTGGGATTACAGGC T A AF131215.6,XKR6 Ensembl:ENSG00000269918,Ensembl:ENSG00000171044 lincRNA,Protein coding exon,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1302403008 Functional Loss SNV dbSNP153 33..33 33 - - - 44348 RMVar_ID_44348 Human_SNP_ID_351913839 A-to-I Human chr8 - 11106701 11106700 11106701 GGACCACAGGTGCCCACCACCATGCCCAGCTAATTTTTTGTATTTTTAGTAGAGACAGGGTTTCA GGACCACAGGTGCCCACCACCATGCCCAGCTA_TTTTTTGTATTTTTAGTAGAGACAGGGTTTCA AT A AF131215.6,XKR6 Ensembl:ENSG00000269918,Ensembl:ENSG00000171044 lincRNA,Protein coding exon,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1227324599 Functional Loss DEL dbSNP153 33..33 33 - - - 44349 RMVar_ID_44349 Human_SNP_ID_351913847 A-to-I Human chr8 - 11106728 11106728 11106728 CTCCTGCCTCAGCCTCCTGAGTAGCTGGGACCACAGGTGCCCACCACCATGCCCAGCTAATTTTT CTCCTGCCTCAGCCTCCTGAGTAGCTGGGACCGCAGGTGCCCACCACCATGCCCAGCTAATTTTT T C XKR6 Ensembl:ENSG00000171044 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1300853990 Functional Loss SNV dbSNP153 33..33 33 - - - 44350 RMVar_ID_44350 Human_SNP_ID_351914142 A-to-I Human chr8 - 11107338 11107338 11107338 AAAATCAGCTGGGCATGGTGGTGTGCACTTGTAGTCTCAGCTGTTTGAGAGGCTGAGGCAGGAGG AAAATCAGCTGGGCATGGTGGTGTGCACTTGTTGTCTCAGCTGTTTGAGAGGCTGAGGCAGGAGG T A XKR6 Ensembl:ENSG00000171044 Protein coding intron GSE38233;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;ASD brains,frontal_cortex;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,30559470,31158229,31158229 RNA-Seq:(High) rs1005118039 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3870867 44351 RMVar_ID_44351 Human_SNP_ID_351914143 A-to-I Human chr8 - 11107338 11107338 11107338 AAAATCAGCTGGGCATGGTGGTGTGCACTTGTAGTCTCAGCTGTTTGAGAGGCTGAGGCAGGAGG AAAATCAGCTGGGCATGGTGGTGTGCACTTGTGGTCTCAGCTGTTTGAGAGGCTGAGGCAGGAGG T C XKR6 Ensembl:ENSG00000171044 Protein coding intron GSE38233;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;ASD brains,frontal_cortex;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,30559470,31158229,31158229 RNA-Seq:(High) rs1005118039 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3870867 44352 RMVar_ID_44352 Human_SNP_ID_351914180 A-to-I Human chr8 - 11107418 11107418 11107418 CACTCTGGGAGGCCGAGGCAGGAGGACTGCCCAAGGCCAGGAGTTAACATAGCAGGACCCTGTCT CACTCTGGGAGGCCGAGGCAGGAGGACTGCCCGAGGCCAGGAGTTAACATAGCAGGACCCTGTCT T C XKR6 Ensembl:ENSG00000171044 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1354083264 Functional Loss SNV dbSNP153 33..33 33 - - - 44353 RMVar_ID_44353 Human_SNP_ID_351921778 A-to-I Human chr8 - 11127029 11127029 11127029 TAACCCTGTTGTAAAGAATGATACACAAGACAAACTTACCCTGATGTTGTTAAATATATGTTAGA TAACCCTGTTGTAAAGAATGATACACAAGACAGACTTACCCTGATGTTGTTAAATATATGTTAGA T C XKR6 Ensembl:ENSG00000171044 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1291680583 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18520722 44354 RMVar_ID_44354 Human_SNP_ID_351921785 A-to-I Human chr8 - 11127049 11127049 11127049 TACTCTACTGTCCTAGAGTATAACCCTGTTGTAAAGAATGATACACAAGACAAACTTACCCTGAT TACTCTACTGTCCTAGAGTATAACCCTGTTGTGAAGAATGATACACAAGACAAACTTACCCTGAT T C XKR6 Ensembl:ENSG00000171044 Protein coding intron GSE47997;GSE107867 K562 cells&HepG2 cells;ASD brains,cerebellum - 23474544,30559470 RNA-Seq:(High) rs1159189174 Functional Loss SNV dbSNP153 33..33 33 - - - 44355 RMVar_ID_44355 Human_SNP_ID_351921789 A-to-I Human chr8 - 11127062 11127062 11127062 AGAGTACCCTTAGTACTCTACTGTCCTAGAGTATAACCCTGTTGTAAAGAATGATACACAAGACA AGAGTACCCTTAGTACTCTACTGTCCTAGAGTGTAACCCTGTTGTAAAGAATGATACACAAGACA T C XKR6 Ensembl:ENSG00000171044 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs886331428 Functional Loss SNV dbSNP153 33..33 33 - - - 44356 RMVar_ID_44356 Human_SNP_ID_351921796 A-to-I Human chr8 - 11127075 11127075 11127075 CAATGTACCACCTAGAGTACCCTTAGTACTCTACTGTCCTAGAGTATAACCCTGTTGTAAAGAAT CAATGTACCACCTAGAGTACCCTTAGTACTCTTCTGTCCTAGAGTATAACCCTGTTGTAAAGAAT T A XKR6 Ensembl:ENSG00000171044 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs986674559 Functional Loss SNV dbSNP153 33..33 33 - - - 44357 RMVar_ID_44357 Human_SNP_ID_351921797 A-to-I Human chr8 - 11127075 11127075 11127075 CAATGTACCACCTAGAGTACCCTTAGTACTCTACTGTCCTAGAGTATAACCCTGTTGTAAAGAAT CAATGTACCACCTAGAGTACCCTTAGTACTCTGCTGTCCTAGAGTATAACCCTGTTGTAAAGAAT T C XKR6 Ensembl:ENSG00000171044 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs986674559 Functional Loss SNV dbSNP153 33..33 33 - - - 44358 RMVar_ID_44358 Human_SNP_ID_351922331 A-to-I Human chr8 - 11128641 11128641 11128641 TCATCTTGTGTATCATTCTCTACAACAGGGTTATACTCTAGGACAGTAGAGTACTGCGGGTACTC TCATCTTGTGTATCATTCTCTACAACAGGGTTTTACTCTAGGACAGTAGAGTACTGCGGGTACTC T A XKR6 Ensembl:ENSG00000171044 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1160009994 Functional Loss SNV dbSNP153 33..33 33 - - - 44359 RMVar_ID_44359 Human_SNP_ID_351922332 A-to-I Human chr8 - 11128641 11128641 11128641 TCATCTTGTGTATCATTCTCTACAACAGGGTTATACTCTAGGACAGTAGAGTACTGCGGGTACTC TCATCTTGTGTATCATTCTCTACAACAGGGTTGTACTCTAGGACAGTAGAGTACTGCGGGTACTC T C XKR6 Ensembl:ENSG00000171044 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1160009994 Functional Loss SNV dbSNP153 33..33 33 - - - 44360 RMVar_ID_44360 Human_SNP_ID_351922338 A-to-I Human chr8 - 11128659 11128659 11128659 AACAACATCAGGGTAATTTCATCTTGTGTATCATTCTCTACAACAGGGTTATACTCTAGGACAGT AACAACATCAGGGTAATTTCATCTTGTGTATCGTTCTCTACAACAGGGTTATACTCTAGGACAGT T C XKR6 Ensembl:ENSG00000171044 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1483991547 Functional Loss SNV dbSNP153 33..33 33 - - - 44361 RMVar_ID_44361 Human_SNP_ID_351922342 A-to-I Human chr8 - 11128671 11128671 11128671 GAACAGCCATTTAACAACATCAGGGTAATTTCATCTTGTGTATCATTCTCTACAACAGGGTTATA GAACAGCCATTTAACAACATCAGGGTAATTTCTTCTTGTGTATCATTCTCTACAACAGGGTTATA T A XKR6 Ensembl:ENSG00000171044 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs774038984 Functional Loss SNV dbSNP153 33..33 33 - - - 44362 RMVar_ID_44362 Human_SNP_ID_351933374 A-to-I Human chr8 - 11159661 11159661 11159661 ACTGGTCTGCATCAGAATGACTTGGAGGACTTATCAAAACACAGATTGCCAGGCCCCACCTGAAG ACTGGTCTGCATCAGAATGACTTGGAGGACTTGTCAAAACACAGATTGCCAGGCCCCACCTGAAG T C XKR6 Ensembl:ENSG00000171044 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1034239999 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16319353 44363 RMVar_ID_44363 Human_SNP_ID_351940247 A-to-I Human chr8 - 11178971 11178971 11178971 AGGTGTGGTCGTGTATGCCTGTAGTTCTAGCTACTTGGGAGGCTGAGGCGGGAAGATTATTTGAG AGGTGTGGTCGTGTATGCCTGTAGTTCTAGCTGCTTGGGAGGCTGAGGCGGGAAGATTATTTGAG T C XKR6 Ensembl:ENSG00000171044 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs933720036 Functional Loss SNV dbSNP153 33..33 33 - - - 44364 RMVar_ID_44364 Human_SNP_ID_351940692 A-to-I Human chr8 - 11180082 11180082 11180082 ATGCTGGAGTGCAGTGGTGCTTATCATAGCTCACTGCAACCTCAACCTCCCAGGCTCAAACAGTT ATGCTGGAGTGCAGTGGTGCTTATCATAGCTCGCTGCAACCTCAACCTCCCAGGCTCAAACAGTT T C XKR6 Ensembl:ENSG00000171044 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1054990231 Functional Loss SNV dbSNP153 33..33 33 - - - 44365 RMVar_ID_44365 Human_SNP_ID_352028465 A-to-I Human chr8 - 11424494 11424494 11424494 CAACGATGCCACCTACGAGCTGGAGGAGCGGGATGAGCTGGCCGACCTCTTCTGTGACTCCCCTC CAACGATGCCACCTACGAGCTGGAGGAGCGGGGTGAGCTGGCCGACCTCTTCTGTGACTCCCCTC T C FAM167A Ensembl:ENSG00000154319 Protein coding CDS GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs750839979 Functional Loss SNV dbSNP153 33..33 33 - - - 44366 RMVar_ID_44366 Human_SNP_ID_352156668 A-to-I Human chr8 + 11786874 11786874 11786874 ATTTGCCAGGCTGGTTTGAACTCCTACAACTCAAGCATTCCTCCCACCTTGGTCTCCCAAAATGT ATTTGCCAGGCTGGTTTGAACTCCTACAACTCTAGCATTCCTCCCACCTTGGTCTCCCAAAATGT A T NEIL2 Ensembl:ENSG00000154328 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1384477274 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16322462 Human_miRNA_ID_2697164,Human_miRNA_ID_3077487 RMVar_hsa_circ_77367,RMVar_hsa_circ_250232,RMVar_hsa_circ_118361,RMVar_hsa_circ_250233 44367 RMVar_ID_44367 Human_SNP_ID_352175492 A-to-I Human chr8 + 11822623 11822623 11822623 ATCATTTGAGCCCAGGAGTTAGACACAAGCCTAAGCAACATAGCGAGACCCCGTCTTTCAAAAAA ATCATTTGAGCCCAGGAGTTAGACACAAGCCTGAGCAACATAGCGAGACCCCGTCTTTCAAAAAA A G FDFT1 Ensembl:ENSG00000079459 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs964698581 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_250238,RMVar_hsa_circ_94262,RMVar_hsa_circ_288437,RMVar_hsa_circ_250236,RMVar_hsa_circ_294723,RMVar_hsa_circ_22907,RMVar_hsa_circ_266866,RMVar_hsa_circ_250239,RMVar_hsa_circ_331005,RMVar_hsa_circ_346729,RMVar_hsa_circ_250237,RMVar_hsa_circ_344505,RMVar_hsa_circ_364421,RMVar_hsa_circ_250242 44368 RMVar_ID_44368 Human_SNP_ID_352176709 A-to-I Human chr8 + 11824987 11824987 11824987 TTGATCTCCTGATCTCGTGATCCGCCCGTCTCAGCTTCCCAAAGTGCTGGGATTACAGGCATGAG TTGATCTCCTGATCTCGTGATCCGCCCGTCTCGGCTTCCCAAAGTGCTGGGATTACAGGCATGAG A G FDFT1 Ensembl:ENSG00000079459 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs948839661 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_250238,RMVar_hsa_circ_94262,RMVar_hsa_circ_288437,RMVar_hsa_circ_250236,RMVar_hsa_circ_294723,RMVar_hsa_circ_22907,RMVar_hsa_circ_266866,RMVar_hsa_circ_250239,RMVar_hsa_circ_331005,RMVar_hsa_circ_346729,RMVar_hsa_circ_250237,RMVar_hsa_circ_344505,RMVar_hsa_circ_364421,RMVar_hsa_circ_250242 44369 RMVar_ID_44369 Human_SNP_ID_352176876 A-to-I Human chr8 + 11825317 11825317 11825317 TAATCCCAGCACTTTGGGAGGCCAAGGCTGGCAGATCAGTTGAGGTCAGGAGTTCGAGACCAGCG TAATCCCAGCACTTTGGGAGGCCAAGGCTGGCGGATCAGTTGAGGTCAGGAGTTCGAGACCAGCG A G FDFT1 Ensembl:ENSG00000079459 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1352591654 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_250238,RMVar_hsa_circ_94262,RMVar_hsa_circ_288437,RMVar_hsa_circ_250236,RMVar_hsa_circ_294723,RMVar_hsa_circ_22907,RMVar_hsa_circ_266866,RMVar_hsa_circ_250239,RMVar_hsa_circ_331005,RMVar_hsa_circ_346729,RMVar_hsa_circ_250237,RMVar_hsa_circ_344505,RMVar_hsa_circ_364421,RMVar_hsa_circ_250242 44370 RMVar_ID_44370 Human_SNP_ID_352176970 A-to-I Human chr8 + 11825522 11825521 11825522 AGATTGTGCCAGTGCACTCCAGCCCAGGGGACAAAGTGAGACTTGATCTCAAAAAAAAAAAAAAA AGATTGTGCCAGTGCACTCCAGCCCAGGGGAC_AAGTGAGACTTGATCTCAAAAAAAAAAAAAAA CA C FDFT1 Ensembl:ENSG00000079459 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1400885204 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_250238,RMVar_hsa_circ_94262,RMVar_hsa_circ_288437,RMVar_hsa_circ_250236,RMVar_hsa_circ_294723,RMVar_hsa_circ_22907,RMVar_hsa_circ_266866,RMVar_hsa_circ_250239,RMVar_hsa_circ_331005,RMVar_hsa_circ_346729,RMVar_hsa_circ_250237,RMVar_hsa_circ_344505,RMVar_hsa_circ_364421,RMVar_hsa_circ_250242 44371 RMVar_ID_44371 Human_SNP_ID_352177175 A-to-I Human chr8 + 11825836 11825836 11825836 AAACATCAAATTCCCGTCAGCCAGAGACTGCTATGAAATGTTTTGAGCACATCCTTCTTGAATGT AAACATCAAATTCCCGTCAGCCAGAGACTGCTGTGAAATGTTTTGAGCACATCCTTCTTGAATGT A G FDFT1 Ensembl:ENSG00000079459 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs904012 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_250238,RMVar_hsa_circ_94262,RMVar_hsa_circ_288437,RMVar_hsa_circ_250236,RMVar_hsa_circ_294723,RMVar_hsa_circ_22907,RMVar_hsa_circ_266866,RMVar_hsa_circ_250239,RMVar_hsa_circ_331005,RMVar_hsa_circ_346729,RMVar_hsa_circ_250237,RMVar_hsa_circ_344505,RMVar_hsa_circ_364421,RMVar_hsa_circ_250242 44372 RMVar_ID_44372 Human_SNP_ID_352177585 A-to-I Human chr8 + 11826659 11826652 11826660 AACATCGTGAAACCCCGTGTTTACTAAAAAATACAAAAATTAGCCGGGCGTGGTGGCAAGGGCTT AACATCGTGAAACCCCGTGTTTACTA________AAAAATTAGCCGGGCGTGGTGGCAAGGGCTT AAAAAATAC A FDFT1 Ensembl:ENSG00000079459 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs768271780 Functional Loss DEL dbSNP153 27..34 33 - - - RMVar_hsa_circ_250238,RMVar_hsa_circ_94262,RMVar_hsa_circ_288437,RMVar_hsa_circ_250236,RMVar_hsa_circ_22907,RMVar_hsa_circ_266866,RMVar_hsa_circ_52043,RMVar_hsa_circ_346729,RMVar_hsa_circ_250237,RMVar_hsa_circ_344505,RMVar_hsa_circ_364421,RMVar_hsa_circ_250242 44373 RMVar_ID_44373 Human_SNP_ID_352177587 A-to-I Human chr8 + 11826659 11826659 11826659 AACATCGTGAAACCCCGTGTTTACTAAAAAATACAAAAATTAGCCGGGCGTGGTGGCAAGGGCTT AACATCGTGAAACCCCGTGTTTACTAAAAAATCCAAAAATTAGCCGGGCGTGGTGGCAAGGGCTT A C FDFT1 Ensembl:ENSG00000079459 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1280338991 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_250238,RMVar_hsa_circ_94262,RMVar_hsa_circ_288437,RMVar_hsa_circ_250236,RMVar_hsa_circ_22907,RMVar_hsa_circ_266866,RMVar_hsa_circ_52043,RMVar_hsa_circ_346729,RMVar_hsa_circ_250237,RMVar_hsa_circ_344505,RMVar_hsa_circ_364421,RMVar_hsa_circ_250242 44374 RMVar_ID_44374 Human_SNP_ID_352179405 A-to-I Human chr8 + 11829947 11829947 11829947 TTGACTCACTGCAACCTCCGCCCCCTAGGTTCAAGCAATTCTTCTGTCTCACCCTCCTGAGTAGC TTGACTCACTGCAACCTCCGCCCCCTAGGTTCGAGCAATTCTTCTGTCTCACCCTCCTGAGTAGC A G FDFT1 Ensembl:ENSG00000079459 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs754231701 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_250238,RMVar_hsa_circ_94262,RMVar_hsa_circ_288437,RMVar_hsa_circ_250236,RMVar_hsa_circ_22907,RMVar_hsa_circ_266866,RMVar_hsa_circ_52043,RMVar_hsa_circ_346729,RMVar_hsa_circ_250237,RMVar_hsa_circ_344505,RMVar_hsa_circ_364421,RMVar_hsa_circ_250242 44375 RMVar_ID_44375 Human_SNP_ID_352179440 A-to-I Human chr8 + 11830013 11830013 11830013 GGGATTACAGGCGCCTGCCACCGTACCCGGCTAGTTTTTGTATTTTTAGTAGACACAGGGTTTCA GGGATTACAGGCGCCTGCCACCGTACCCGGCTGGTTTTTGTATTTTTAGTAGACACAGGGTTTCA A G FDFT1 Ensembl:ENSG00000079459 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1002631421 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_250238,RMVar_hsa_circ_94262,RMVar_hsa_circ_288437,RMVar_hsa_circ_250236,RMVar_hsa_circ_22907,RMVar_hsa_circ_266866,RMVar_hsa_circ_52043,RMVar_hsa_circ_346729,RMVar_hsa_circ_250237,RMVar_hsa_circ_344505,RMVar_hsa_circ_364421,RMVar_hsa_circ_250242 44376 RMVar_ID_44376 Human_SNP_ID_352183000 A-to-I Human chr8 + 11836860 11836860 11836860 GAGTTTGAGACCAGCCTGACCAACACTGGTAAAACCTTGTCTCTATTAAAAATGCAAAAATTAGC GAGTTTGAGACCAGCCTGACCAACACTGGTAACACCTTGTCTCTATTAAAAATGCAAAAATTAGC A C FDFT1 Ensembl:ENSG00000079459 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1035480707 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266866,RMVar_hsa_circ_250237 44377 RMVar_ID_44377 Human_SNP_ID_352183231 A-to-I Human chr8 + 11837330 11837330 11837330 TCGGATCACTGCAACCTCCACCTCCCAGGCTCAAGTGATCTTCCCACCCCAGTCCCCAAGTAGCT TCGGATCACTGCAACCTCCACCTCCCAGGCTCCAGTGATCTTCCCACCCCAGTCCCCAAGTAGCT A C FDFT1 Ensembl:ENSG00000079459 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1250387314 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266866,RMVar_hsa_circ_250237 44378 RMVar_ID_44378 Human_SNP_ID_352186290 A-to-I Human chr8 - 11842699 11842699 11842699 CTGGGAGGCAGAGGATGCAGTGAGCCGAGATCACGCCATTGCACTCCAGCCTGGGGGACAAGAGT CTGGGAGGCAGAGGATGCAGTGAGCCGAGATCGCGCCATTGCACTCCAGCCTGGGGGACAAGAGT T C CTSB Ensembl:ENSG00000164733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1138591 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24241952,Human_RBP_ID_26557992 Human_miRNA_ID_1073736,Human_miRNA_ID_2019288,Human_miRNA_ID_2024382,Human_miRNA_ID_2311004,Human_miRNA_ID_2313022,Human_miRNA_ID_2499114,Human_miRNA_ID_2606897,Human_miRNA_ID_2654804 RMVar_hsa_circ_108255,RMVar_hsa_circ_250245 44379 RMVar_ID_44379 Human_SNP_ID_352186295 A-to-I Human chr8 - 11842704 11842704 11842704 TGAACCTGGGAGGCAGAGGATGCAGTGAGCCGAGATCACGCCATTGCACTCCAGCCTGGGGGACA TGAACCTGGGAGGCAGAGGATGCAGTGAGCCGTGATCACGCCATTGCACTCCAGCCTGGGGGACA T A CTSB Ensembl:ENSG00000164733 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1071789 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17578543,Human_RBP_ID_26557992 Human_miRNA_ID_210213,Human_miRNA_ID_1073736,Human_miRNA_ID_2019288,Human_miRNA_ID_2024382,Human_miRNA_ID_2311004,Human_miRNA_ID_2313022,Human_miRNA_ID_2499114,Human_miRNA_ID_2654804 RMVar_hsa_circ_108255,RMVar_hsa_circ_250245 44380 RMVar_ID_44380 Human_SNP_ID_352186296 A-to-I Human chr8 - 11842704 11842704 11842704 TGAACCTGGGAGGCAGAGGATGCAGTGAGCCGAGATCACGCCATTGCACTCCAGCCTGGGGGACA TGAACCTGGGAGGCAGAGGATGCAGTGAGCCGGGATCACGCCATTGCACTCCAGCCTGGGGGACA T C CTSB Ensembl:ENSG00000164733 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1071789 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17578543,Human_RBP_ID_26557992 Human_miRNA_ID_210213,Human_miRNA_ID_1073736,Human_miRNA_ID_2019288,Human_miRNA_ID_2024382,Human_miRNA_ID_2311004,Human_miRNA_ID_2313022,Human_miRNA_ID_2499114,Human_miRNA_ID_2654804 RMVar_hsa_circ_108255,RMVar_hsa_circ_250245 44381 RMVar_ID_44381 Human_SNP_ID_352186303 A-to-I Human chr8 - 11842709 11842709 11842709 TCGCTTGAACCTGGGAGGCAGAGGATGCAGTGAGCCGAGATCACGCCATTGCACTCCAGCCTGGG TCGCTTGAACCTGGGAGGCAGAGGATGCAGTGGGCCGAGATCACGCCATTGCACTCCAGCCTGGG T C CTSB Ensembl:ENSG00000164733 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1071788 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17578543,Human_RBP_ID_26557992 Human_miRNA_ID_679226 RMVar_hsa_circ_108255,RMVar_hsa_circ_250245 44382 RMVar_ID_44382 Human_SNP_ID_352186313 A-to-I Human chr8 - 11842722 11842722 11842722 TGAGGTACGAGAATCGCTTGAACCTGGGAGGCAGAGGATGCAGTGAGCCGAGATCACGCCATTGC TGAGGTACGAGAATCGCTTGAACCTGGGAGGCGGAGGATGCAGTGAGCCGAGATCACGCCATTGC T C CTSB Ensembl:ENSG00000164733 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1071787 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17578543,Human_RBP_ID_26557992 Human_miRNA_ID_2234670,Human_miRNA_ID_3028830 RMVar_hsa_circ_108255,RMVar_hsa_circ_250245 44383 RMVar_ID_44383 Human_SNP_ID_352186323 A-to-I Human chr8 - 11842742 11842742 11842742 ATCCCAGCTACTCGGGAGGCTGAGGTACGAGAATCGCTTGAACCTGGGAGGCAGAGGATGCAGTG ATCCCAGCTACTCGGGAGGCTGAGGTACGAGAGTCGCTTGAACCTGGGAGGCAGAGGATGCAGTG T C CTSB Ensembl:ENSG00000164733 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1071784 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17578543,Human_RBP_ID_26557992 RMVar_hsa_circ_108255,RMVar_hsa_circ_250245 44384 RMVar_ID_44384 Human_SNP_ID_352186332 A-to-I Human chr8 - 11842752 11842752 11842752 CATGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGTACGAGAATCGCTTGAACCTGGGAGGCAGA CATGCCTGTAATCCCAGCTACTCGGGAGGCTGGGGTACGAGAATCGCTTGAACCTGGGAGGCAGA T C CTSB Ensembl:ENSG00000164733 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1071783 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17578543,Human_RBP_ID_26553098 RMVar_hsa_circ_108255,RMVar_hsa_circ_250245 44385 RMVar_ID_44385 Human_SNP_ID_352186350 A-to-I Human chr8 - 11842775 11842775 11842775 AAAATTAGCCAAGCATGCTGGCACATGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGTACGAGA AAAATTAGCCAAGCATGCTGGCACATGCCTGTGATCCCAGCTACTCGGGAGGCTGAGGTACGAGA T C CTSB Ensembl:ENSG00000164733 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1138564 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26557992 RMVar_hsa_circ_108255,RMVar_hsa_circ_250245 44386 RMVar_ID_44386 Human_SNP_ID_352186361 A-to-I Human chr8 - 11842796 11842796 11842796 CCCCATCTCTACTAAAAATACAAAATTAGCCAAGCATGCTGGCACATGCCTGTAATCCCAGCTAC CCCCATCTCTACTAAAAATACAAAATTAGCCAGGCATGCTGGCACATGCCTGTAATCCCAGCTAC T C CTSB Ensembl:ENSG00000164733 Protein coding intron GSE38233;GSE112787 cultured B-cells;293 Flip-In T-REx cells,empty vector - 24183664,29967493 RNA-Seq:(High) rs1138558 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26557992 RMVar_hsa_circ_108255,RMVar_hsa_circ_250245 44387 RMVar_ID_44387 Human_SNP_ID_352186368 A-to-I Human chr8 - 11842801 11842801 11842801 TGAAACCCCATCTCTACTAAAAATACAAAATTAGCCAAGCATGCTGGCACATGCCTGTAATCCCA TGAAACCCCATCTCTACTAAAAATACAAAATTTGCCAAGCATGCTGGCACATGCCTGTAATCCCA T A CTSB Ensembl:ENSG00000164733 Protein coding intron GSE38233;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,32596459 RNA-Seq:(High) rs1384424435 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26557992 RMVar_hsa_circ_108255,RMVar_hsa_circ_250245 44388 RMVar_ID_44388 Human_SNP_ID_352186377 A-to-I Human chr8 - 11842812 11842812 11842812 TGGCAACACGGTGAAACCCCATCTCTACTAAAAATACAAAATTAGCCAAGCATGCTGGCACATGC TGGCAACACGGTGAAACCCCATCTCTACTAAAGATACAAAATTAGCCAAGCATGCTGGCACATGC T C CTSB Ensembl:ENSG00000164733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1138553 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108255,RMVar_hsa_circ_250245 44389 RMVar_ID_44389 Human_SNP_ID_352186381 A-to-I Human chr8 - 11842815 11842815 11842815 CCTTGGCAACACGGTGAAACCCCATCTCTACTAAAAATACAAAATTAGCCAAGCATGCTGGCACA CCTTGGCAACACGGTGAAACCCCATCTCTACTGAAAATACAAAATTAGCCAAGCATGCTGGCACA T C CTSB Ensembl:ENSG00000164733 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1138550 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108255,RMVar_hsa_circ_250245 44390 RMVar_ID_44390 Human_SNP_ID_352186405 A-to-I Human chr8 - 11842854 11842854 11842854 GGCGGGCAGATCACCTGAGGTCAGGAGTTTTGAGATCAGCCTTGGCAACACGGTGAAACCCCATC GGCGGGCAGATCACCTGAGGTCAGGAGTTTTGGGATCAGCCTTGGCAACACGGTGAAACCCCATC T C CTSB Ensembl:ENSG00000164733 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1071782 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24391229,Human_RBP_ID_26557993 RMVar_hsa_circ_108255,RMVar_hsa_circ_250245 44391 RMVar_ID_44391 Human_SNP_ID_352186406 A-to-I Human chr8 - 11842854 11842854 11842854 GGCGGGCAGATCACCTGAGGTCAGGAGTTTTGAGATCAGCCTTGGCAACACGGTGAAACCCCATC GGCGGGCAGATCACCTGAGGTCAGGAGTTTTGCGATCAGCCTTGGCAACACGGTGAAACCCCATC T G CTSB Ensembl:ENSG00000164733 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1071782 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24391229,Human_RBP_ID_26557993 RMVar_hsa_circ_108255,RMVar_hsa_circ_250245 44392 RMVar_ID_44392 Human_SNP_ID_352186410 A-to-I Human chr8 - 11842864 11842864 11842864 GGGAGGCTGAGGCGGGCAGATCACCTGAGGTCAGGAGTTTTGAGATCAGCCTTGGCAACACGGTG GGGAGGCTGAGGCGGGCAGATCACCTGAGGTCGGGAGTTTTGAGATCAGCCTTGGCAACACGGTG T C CTSB Ensembl:ENSG00000164733 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1198850034 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24391229 RMVar_hsa_circ_108255,RMVar_hsa_circ_250245 44393 RMVar_ID_44393 Human_SNP_ID_352186423 A-to-I Human chr8 - 11842887 11842887 11842887 CAAGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGCAGATCACCTGAGGTCAGGAGTTTTG CAAGCCTGTAATCCCAGCACTTTGGGAGGCTGCGGCGGGCAGATCACCTGAGGTCAGGAGTTTTG T G CTSB Ensembl:ENSG00000164733 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1009595594 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108255,RMVar_hsa_circ_250245 44394 RMVar_ID_44394 Human_SNP_ID_352186431 A-to-I Human chr8 - 11842909 11842909 11842909 AAAAAGGCCGGGCGCAGTGGCTCAAGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGCAGA AAAAAGGCCGGGCGCAGTGGCTCAAGCCTGTAGTCCCAGCACTTTGGGAGGCTGAGGCGGGCAGA T C CTSB Ensembl:ENSG00000164733 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1056057597 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108255,RMVar_hsa_circ_250245 44395 RMVar_ID_44395 Human_SNP_ID_352186432 A-to-I Human chr8 - 11842910 11842910 11842910 AAAAAAGGCCGGGCGCAGTGGCTCAAGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGCAG AAAAAAGGCCGGGCGCAGTGGCTCAAGCCTGTGATCCCAGCACTTTGGGAGGCTGAGGCGGGCAG T C CTSB Ensembl:ENSG00000164733 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs778278521 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108255,RMVar_hsa_circ_250245 44396 RMVar_ID_44396 Human_SNP_ID_352186433 A-to-I Human chr8 - 11842910 11842910 11842910 AAAAAAGGCCGGGCGCAGTGGCTCAAGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGCAG AAAAAAGGCCGGGCGCAGTGGCTCAAGCCTGTCATCCCAGCACTTTGGGAGGCTGAGGCGGGCAG T G CTSB Ensembl:ENSG00000164733 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs778278521 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108255,RMVar_hsa_circ_250245 44397 RMVar_ID_44397 Human_SNP_ID_352186595 A-to-I Human chr8 - 11843077 11843077 11843077 GGGCATGGTGGCACATGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAA GGGCATGGTGGCACATGCCTGTAATCCCAGCTGCTTGGGAGGCTGAGGCAGGAGAATCGCTTGAA T C CTSB Ensembl:ENSG00000164733 Protein coding intron GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,31158229,31158229 RNA-Seq:(High) rs1071821 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108255,RMVar_hsa_circ_250245 44398 RMVar_ID_44398 Human_SNP_ID_352186601 A-to-I Human chr8 - 11843086 11843086 11843086 AAATTAGCTGGGCATGGTGGCACATGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAA AAATTAGCTGGGCATGGTGGCACATGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAA T C CTSB Ensembl:ENSG00000164733 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1071813 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108255,RMVar_hsa_circ_250245 44399 RMVar_ID_44399 Human_SNP_ID_352186602 A-to-I Human chr8 - 11843087 11843087 11843087 AAAATTAGCTGGGCATGGTGGCACATGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGA AAAATTAGCTGGGCATGGTGGCACATGCCTGTGATCCCAGCTACTTGGGAGGCTGAGGCAGGAGA T C CTSB Ensembl:ENSG00000164733 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs1138540 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108255,RMVar_hsa_circ_250245 44400 RMVar_ID_44400 Human_SNP_ID_352186626 A-to-I Human chr8 - 11843122 11843122 11843122 CAACATGCTGAAACCTCACCTCTACTAAAAATACAAAAATTAGCTGGGCATGGTGGCACATGCCT CAACATGCTGAAACCTCACCTCTACTAAAAATGCAAAAATTAGCTGGGCATGGTGGCACATGCCT T C CTSB Ensembl:ENSG00000164733 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1142991 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108255,RMVar_hsa_circ_250245 44401 RMVar_ID_44401 Human_SNP_ID_352186628 A-to-I Human chr8 - 11843125 11843125 11843125 GGCCAACATGCTGAAACCTCACCTCTACTAAAAATACAAAAATTAGCTGGGCATGGTGGCACATG GGCCAACATGCTGAAACCTCACCTCTACTAAAGATACAAAAATTAGCTGGGCATGGTGGCACATG T C CTSB Ensembl:ENSG00000164733 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1016167452 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108255,RMVar_hsa_circ_250245 44402 RMVar_ID_44402 Human_SNP_ID_352186630 A-to-I Human chr8 - 11843128 11843128 11843128 CCTGGCCAACATGCTGAAACCTCACCTCTACTAAAAATACAAAAATTAGCTGGGCATGGTGGCAC CCTGGCCAACATGCTGAAACCTCACCTCTACTGAAAATACAAAAATTAGCTGGGCATGGTGGCAC T C CTSB Ensembl:ENSG00000164733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1142985 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108255,RMVar_hsa_circ_250245 44403 RMVar_ID_44403 Human_SNP_ID_352186653 A-to-I Human chr8 - 11843167 11843167 11843167 CAAGGTGGGAGGATGACAAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGCTGAAACCTCACC CAAGGTGGGAGGATGACAAGGTCAGGAGTTCAGGACCAGCCTGGCCAACATGCTGAAACCTCACC T C CTSB Ensembl:ENSG00000164733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1142965 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108255,RMVar_hsa_circ_250245 44404 RMVar_ID_44404 Human_SNP_ID_352186656 A-to-I Human chr8 - 11843176 11843176 11843176 TTGGGAGGCCAAGGTGGGAGGATGACAAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGCTGA TTGGGAGGCCAAGGTGGGAGGATGACAAGGTCGGGAGTTCAAGACCAGCCTGGCCAACATGCTGA T C CTSB Ensembl:ENSG00000164733 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1142963 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108255,RMVar_hsa_circ_250245 44405 RMVar_ID_44405 Human_SNP_ID_352186993 A-to-I Human chr8 - 11843774 11843774 11843774 TGCCTGCCTCAGCCTCCCAAAGTGTTGGGATTACAGGCGTGAGCCACTGGGCCCTGCCTGTATTT TGCCTGCCTCAGCCTCCCAAAGTGTTGGGATTGCAGGCGTGAGCCACTGGGCCCTGCCTGTATTT T C CTSB Ensembl:ENSG00000164733 Protein coding intron GSE47997;GSE100210;GSE99789;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,29129909,29796672,30559470,31158229,31158229,31158229 RNA-Seq:(High) rs879175042 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108255,RMVar_hsa_circ_250245 44406 RMVar_ID_44406 Human_SNP_ID_352186998 A-to-I Human chr8 - 11843786 11843786 11843786 CCTCAGGTGGTCTGCCTGCCTCAGCCTCCCAAAGTGTTGGGATTACAGGCGTGAGCCACTGGGCC CCTCAGGTGGTCTGCCTGCCTCAGCCTCCCAAGGTGTTGGGATTACAGGCGTGAGCCACTGGGCC T C CTSB Ensembl:ENSG00000164733 Protein coding intron GSE47997;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829 K562 cells&HepG2 cells;ASD brains,temporal_cortex;Bronchiolar epithelium,BEP2D cell line - 23474544,30559470,31158229 RNA-Seq:(High) rs1295892042 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108255,RMVar_hsa_circ_250245 44407 RMVar_ID_44407 Human_SNP_ID_352186999 A-to-I Human chr8 - 11843786 11843786 11843786 CCTCAGGTGGTCTGCCTGCCTCAGCCTCCCAAAGTGTTGGGATTACAGGCGTGAGCCACTGGGCC CCTCAGGTGGTCTGCCTGCCTCAGCCTCCCAACGTGTTGGGATTACAGGCGTGAGCCACTGGGCC T G CTSB Ensembl:ENSG00000164733 Protein coding intron GSE47997;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829 K562 cells&HepG2 cells;ASD brains,temporal_cortex;Bronchiolar epithelium,BEP2D cell line - 23474544,30559470,31158229 RNA-Seq:(High) rs1295892042 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108255,RMVar_hsa_circ_250245 44408 RMVar_ID_44408 Human_SNP_ID_352187005 A-to-I Human chr8 - 11843796 11843796 11843796 AAACTCCCGGCCTCAGGTGGTCTGCCTGCCTCAGCCTCCCAAAGTGTTGGGATTACAGGCGTGAG AAACTCCCGGCCTCAGGTGGTCTGCCTGCCTCGGCCTCCCAAAGTGTTGGGATTACAGGCGTGAG T C CTSB Ensembl:ENSG00000164733 Protein coding intron GSE47997;GSE126723:GSM3611827,GSM3611828,GSM3611829 K562 cells&HepG2 cells;Bronchiolar epithelium,BEP2D cell line - 23474544,31158229 RNA-Seq:(High) rs1382529043 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108255,RMVar_hsa_circ_250245 44409 RMVar_ID_44409 Human_SNP_ID_352187016 A-to-I Human chr8 - 11843814 11843814 11843814 GTTGGCCAGGCTAGTTTCAAACTCCCGGCCTCAGGTGGTCTGCCTGCCTCAGCCTCCCAAAGTGT GTTGGCCAGGCTAGTTTCAAACTCCCGGCCTCGGGTGGTCTGCCTGCCTCAGCCTCCCAAAGTGT T C CTSB Ensembl:ENSG00000164733 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1338722439 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108255,RMVar_hsa_circ_250245 44410 RMVar_ID_44410 Human_SNP_ID_352187029 A-to-I Human chr8 - 11843828 11843828 11843828 CAGGATTTCACCATGTTGGCCAGGCTAGTTTCAAACTCCCGGCCTCAGGTGGTCTGCCTGCCTCA CAGGATTTCACCATGTTGGCCAGGCTAGTTTCGAACTCCCGGCCTCAGGTGGTCTGCCTGCCTCA T C CTSB Ensembl:ENSG00000164733 Protein coding intron GSE47997;GSE38233;GSE107867;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;ASD brains,Fragile X samples from NIH NeuroBioBank;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,30559470,32596459 RNA-Seq:(High) rs1195033576 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108255,RMVar_hsa_circ_250245 44411 RMVar_ID_44411 Human_SNP_ID_352187033 A-to-I Human chr8 - 11843834 11843834 11843834 TACATACAGGATTTCACCATGTTGGCCAGGCTAGTTTCAAACTCCCGGCCTCAGGTGGTCTGCCT TACATACAGGATTTCACCATGTTGGCCAGGCTGGTTTCAAACTCCCGGCCTCAGGTGGTCTGCCT T C CTSB Ensembl:ENSG00000164733 Protein coding intron GSE47997;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,31158229,31158229,32596459 RNA-Seq:(High) rs1365142633 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108255,RMVar_hsa_circ_250245 44412 RMVar_ID_44412 Human_SNP_ID_352187057 A-to-I Human chr8 - 11843883 11843883 11843883 GGATGACAGGCACTCACCAATATGCCTGGGTAATTTTTGTATTTTTAAGTACATACAGGATTTCA GGATGACAGGCACTCACCAATATGCCTGGGTAGTTTTTGTATTTTTAAGTACATACAGGATTTCA T C CTSB Ensembl:ENSG00000164733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs955100752 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17578545,Human_RBP_ID_26558001 RMVar_hsa_circ_108255,RMVar_hsa_circ_250245 44413 RMVar_ID_44413 Human_SNP_ID_352187082 A-to-I Human chr8 - 11843910 11843910 11843910 CTCCTGCTTCAGCCTTCCGAGTAGCTGGGATGACAGGCACTCACCAATATGCCTGGGTAATTTTT CTCCTGCTTCAGCCTTCCGAGTAGCTGGGATGGCAGGCACTCACCAATATGCCTGGGTAATTTTT T C CTSB Ensembl:ENSG00000164733 Protein coding intron GSE47997;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,31158229,32596459 RNA-Seq:(High) rs1216113311 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17578545,Human_RBP_ID_22372485,Human_RBP_ID_26558001 RMVar_hsa_circ_108255,RMVar_hsa_circ_250245 44414 RMVar_ID_44414 Human_SNP_ID_352187084 A-to-I Human chr8 - 11843920 11843920 11843920 TCAAGCGATTCTCCTGCTTCAGCCTTCCGAGTAGCTGGGATGACAGGCACTCACCAATATGCCTG TCAAGCGATTCTCCTGCTTCAGCCTTCCGAGTGGCTGGGATGACAGGCACTCACCAATATGCCTG T C CTSB Ensembl:ENSG00000164733 Protein coding intron GSE47997;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,29129909,31158229,32596459 RNA-Seq:(High) rs1464077075 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17578545,Human_RBP_ID_22372485,Human_RBP_ID_26558001 RMVar_hsa_circ_108255,RMVar_hsa_circ_250245 44415 RMVar_ID_44415 Human_SNP_ID_352187094 A-to-I Human chr8 - 11843932 11843932 11843932 AGCCTCCTAGATTCAAGCGATTCTCCTGCTTCAGCCTTCCGAGTAGCTGGGATGACAGGCACTCA AGCCTCCTAGATTCAAGCGATTCTCCTGCTTCTGCCTTCCGAGTAGCTGGGATGACAGGCACTCA T A CTSB Ensembl:ENSG00000164733 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs150223418 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17578545,Human_RBP_ID_22372485,Human_RBP_ID_26558417 RMVar_hsa_circ_108255,RMVar_hsa_circ_250245 44416 RMVar_ID_44416 Human_SNP_ID_352187095 A-to-I Human chr8 - 11843932 11843932 11843932 AGCCTCCTAGATTCAAGCGATTCTCCTGCTTCAGCCTTCCGAGTAGCTGGGATGACAGGCACTCA AGCCTCCTAGATTCAAGCGATTCTCCTGCTTCGGCCTTCCGAGTAGCTGGGATGACAGGCACTCA T C CTSB Ensembl:ENSG00000164733 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs150223418 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17578545,Human_RBP_ID_22372485,Human_RBP_ID_26558417 RMVar_hsa_circ_108255,RMVar_hsa_circ_250245 44417 RMVar_ID_44417 Human_SNP_ID_352187106 A-to-I Human chr8 - 11843949 11843949 11843949 AGCTCACTGCAACCTGCAGCCTCCTAGATTCAAGCGATTCTCCTGCTTCAGCCTTCCGAGTAGCT AGCTCACTGCAACCTGCAGCCTCCTAGATTCAGGCGATTCTCCTGCTTCAGCCTTCCGAGTAGCT T C CTSB Ensembl:ENSG00000164733 Protein coding intron GSE47997;GSE38233;GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;cultured B-cells;cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,24183664,24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs879146162 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4968716,Human_RBP_ID_17578545 RMVar_hsa_circ_108255,RMVar_hsa_circ_250245 44418 RMVar_ID_44418 Human_SNP_ID_352187113 A-to-I Human chr8 - 11843970 11843963 11843970 GGAGTGCAGTGGCGCCTTCTCAGCTCACTGCAACCTGCAGCCTCCTAGATTCAAGCGATTCTCCT GGAGTGCAGTGGCGCCTTCTCAGCTCACTGCA_______GCCTCCTAGATTCAAGCGATTCTCCT CTGCAGGT C CTSB Ensembl:ENSG00000164733 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1441615176 Functional Loss DEL dbSNP153 33..39 33 - - - Human_miRNA_ID_1037365 RMVar_hsa_circ_108255,RMVar_hsa_circ_250245 44419 RMVar_ID_44419 Human_SNP_ID_352187114 A-to-I Human chr8 - 11843964 11843964 11843964 CAGTGGCGCCTTCTCAGCTCACTGCAACCTGCAGCCTCCTAGATTCAAGCGATTCTCCTGCTTCA CAGTGGCGCCTTCTCAGCTCACTGCAACCTGCGGCCTCCTAGATTCAAGCGATTCTCCTGCTTCA T C CTSB Ensembl:ENSG00000164733 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1431943168 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1037365 RMVar_hsa_circ_108255,RMVar_hsa_circ_250245 44420 RMVar_ID_44420 Human_SNP_ID_352187118 A-to-I Human chr8 - 11843970 11843970 11843970 GGAGTGCAGTGGCGCCTTCTCAGCTCACTGCAACCTGCAGCCTCCTAGATTCAAGCGATTCTCCT GGAGTGCAGTGGCGCCTTCTCAGCTCACTGCAGCCTGCAGCCTCCTAGATTCAAGCGATTCTCCT T C CTSB Ensembl:ENSG00000164733 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1392190264 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1037365 RMVar_hsa_circ_108255,RMVar_hsa_circ_250245 44421 RMVar_ID_44421 Human_SNP_ID_352187123 A-to-I Human chr8 - 11843981 11843981 11843981 TCTCCCAGGCTGGAGTGCAGTGGCGCCTTCTCAGCTCACTGCAACCTGCAGCCTCCTAGATTCAA TCTCCCAGGCTGGAGTGCAGTGGCGCCTTCTCGGCTCACTGCAACCTGCAGCCTCCTAGATTCAA T C CTSB Ensembl:ENSG00000164733 Protein coding intron GSE100210;GSE99789;GSE112787 HepG2 cell line;esophageal squamous carcinoma cells,EC109;293 Flip-In T-REx cells,empty vector - 29129909,29796672,29967493 RNA-Seq:(High) rs878997016 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22372486,Human_RBP_ID_23315845,Human_RBP_ID_26558002 Human_miRNA_ID_867804,Human_miRNA_ID_1037365,Human_miRNA_ID_1795890 RMVar_hsa_circ_108255,RMVar_hsa_circ_250245 44422 RMVar_ID_44422 Human_SNP_ID_352187124 A-to-I Human chr8 - 11843981 11843981 11843981 TCTCCCAGGCTGGAGTGCAGTGGCGCCTTCTCAGCTCACTGCAACCTGCAGCCTCCTAGATTCAA TCTCCCAGGCTGGAGTGCAGTGGCGCCTTCTCCGCTCACTGCAACCTGCAGCCTCCTAGATTCAA T G CTSB Ensembl:ENSG00000164733 Protein coding intron GSE100210;GSE99789;GSE112787 HepG2 cell line;esophageal squamous carcinoma cells,EC109;293 Flip-In T-REx cells,empty vector - 29129909,29796672,29967493 RNA-Seq:(High) rs878997016 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22372486,Human_RBP_ID_23315845,Human_RBP_ID_26558002 Human_miRNA_ID_867804,Human_miRNA_ID_1037365,Human_miRNA_ID_1795890 RMVar_hsa_circ_108255,RMVar_hsa_circ_250245 44423 RMVar_ID_44423 Human_SNP_ID_352187134 A-to-I Human chr8 - 11843995 11843995 11843995 AGAGTGAGATTCCGTCTCCCAGGCTGGAGTGCAGTGGCGCCTTCTCAGCTCACTGCAACCTGCAG AGAGTGAGATTCCGTCTCCCAGGCTGGAGTGCGGTGGCGCCTTCTCAGCTCACTGCAACCTGCAG T C CTSB Ensembl:ENSG00000164733 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1143592 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22372486,Human_RBP_ID_26558002 Human_miRNA_ID_622443,Human_miRNA_ID_2854437,Human_miRNA_ID_2857116 RMVar_hsa_circ_108255,RMVar_hsa_circ_250245 44424 RMVar_ID_44424 Human_SNP_ID_352187163 A-to-I Human chr8 - 11844027 11844026 11844028 TGCTCTATTTTTTTGTTGTTGTTGTGACTGACAGAGTGAGATTCCGTCTCCCAGGCTGGAGTGCA TGCTCTATTTTTTTGTTGTTGTTGTGACTGA__GAGTGAGATTCCGTCTCCCAGGCTGGAGTGCA CTG C CTSB Ensembl:ENSG00000164733 Protein coding 3'UTR GSE38233;GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,32596459 RNA-Seq:(High) rs1491421723 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_22372486,Human_RBP_ID_24241954,Human_RBP_ID_26558002 Human_Splice_Rec_949449 Human_miRNA_ID_1535364,Human_miRNA_ID_2230685 RMVar_hsa_circ_108255,RMVar_hsa_circ_250245 44425 RMVar_ID_44425 Human_SNP_ID_352187164 A-to-I Human chr8 - 11844027 11844027 11844027 TGCTCTATTTTTTTGTTGTTGTTGTGACTGACAGAGTGAGATTCCGTCTCCCAGGCTGGAGTGCA TGCTCTATTTTTTTGTTGTTGTTGTGACTGACGGAGTGAGATTCCGTCTCCCAGGCTGGAGTGCA T C CTSB Ensembl:ENSG00000164733 Protein coding 3'UTR GSE38233;GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,32596459 RNA-Seq:(High) rs938779605 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22372486,Human_RBP_ID_24241954,Human_RBP_ID_26558002 Human_Splice_Rec_949449 Human_miRNA_ID_1535364,Human_miRNA_ID_2230685 RMVar_hsa_circ_108255,RMVar_hsa_circ_250245 44426 RMVar_ID_44426 Human_SNP_ID_352191372 A-to-I Human chr8 - 11849867 11849867 11849867 TTTGTTAAGAAAAAAACACAGCCAGGTACGGTAGCTCACGCCTGTAATCTCAACACTTTGGGAGG TTTGTTAAGAAAAAAACACAGCCAGGTACGGTGGCTCACGCCTGTAATCTCAACACTTTGGGAGG T C CTSB Ensembl:ENSG00000164733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170544967 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100951,RMVar_hsa_circ_55110,RMVar_hsa_circ_19822,RMVar_hsa_circ_250247,RMVar_hsa_circ_2156,RMVar_hsa_circ_21333 44427 RMVar_ID_44427 Human_SNP_ID_352194700 A-to-I Human chr8 - 11856504 11856504 11856504 GGTTCAAGTGATTCTACTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCATGCGCCACCACGC GGTTCAAGTGATTCTACTGCCTCAGCCTCCCACGTAGCTGGGATTACAGGCATGCGCCACCACGC T G CTSB Ensembl:ENSG00000164733 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs142972874 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5419,RMVar_hsa_circ_38356,RMVar_hsa_circ_19822,RMVar_hsa_circ_341226,RMVar_hsa_circ_342718,RMVar_hsa_circ_314115,RMVar_hsa_circ_54959,RMVar_hsa_circ_250250,RMVar_hsa_circ_303321,RMVar_hsa_circ_250249,RMVar_hsa_circ_356959,RMVar_hsa_circ_250253,RMVar_hsa_circ_9698,RMVar_hsa_circ_250254,RMVar_hsa_circ_82533,RMVar_hsa_circ_250257 44428 RMVar_ID_44428 Human_SNP_ID_352197164 A-to-I Human chr8 - 11862049 11862049 11862049 GCGCCTGCCACCATGCCTGGCTATTTTTTTGTATTTTTAGTAGAAACGGGGTTTCACCGTGTTAT GCGCCTGCCACCATGCCTGGCTATTTTTTTGTTTTTTTAGTAGAAACGGGGTTTCACCGTGTTAT T A CTSB Ensembl:ENSG00000164733 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1207074158 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5419,RMVar_hsa_circ_342718,RMVar_hsa_circ_314115,RMVar_hsa_circ_250249,RMVar_hsa_circ_356959,RMVar_hsa_circ_9698,RMVar_hsa_circ_250254,RMVar_hsa_circ_82533,RMVar_hsa_circ_250257 44429 RMVar_ID_44429 Human_SNP_ID_352198913 A-to-I Human chr8 - 11865819 11865819 11865819 TATTTTTAGTAGAGACGGGCTTTCACCATGTTAGCCAGGCTGGTTTTCGAACTCCTGATCTCAAG TATTTTTAGTAGAGACGGGCTTTCACCATGTTGGCCAGGCTGGTTTTCGAACTCCTGATCTCAAG T C CTSB Ensembl:ENSG00000164733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1199558386 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16324244 RMVar_hsa_circ_5419,RMVar_hsa_circ_342718,RMVar_hsa_circ_82533,RMVar_hsa_circ_250257 44430 RMVar_ID_44430 Human_SNP_ID_352314878 A-to-I Human chr8 + 12199961 12199958 12199961 AAGGATTTTCTGCCTAATGGTCGGTTCAGCAGAAGATTAAACTGAGCACAGCATCCTGTTCCCTC AAGGATTTTCTGCCTAATGGTCGGTTCAGC___AGATTAAACTGAGCACAGCATCCTGTTCCCTC CAGA C FAM85A RNACentral:URS0000BC43AD lincRNA intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1404068138 Functional Loss DEL dbSNP153 31..33 33 - - - 44431 RMVar_ID_44431 Human_SNP_ID_352376257 A-to-I Human chr8 + 12449211 12449208 12449212 ATGTATATGTGTGTGTGTACACACGCATATATACATACACATGTATATGTGTGTGTGTACACACG ATGTATATGTGTGTGTGTACACACGCATAT____ATACACATGTATATGTGTGTGTGTACACACG TATAC T lnc-ZNF705D-5,FAM66A,LOC100506990,LOC100506990:2,lnc-ZNF705D-7,LOC100506990:3,LOC100506990:4 RNACentral:URS00008B295B,RNACentral:URS00009C0E6F,RNACentral:URS00009BC63E,RNACentral:URS00008B2EB1,RNACentral:URS00008BC4CF,RNACentral:URS000075B46F,RNACentral:URS00009B808D lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron,intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1190025185 Functional Loss DEL dbSNP153 31..34 33 - - - RMVar_hsa_circ_115551,RMVar_hsa_circ_120552,RMVar_hsa_circ_250260,RMVar_hsa_circ_122929,RMVar_hsa_circ_93000,RMVar_hsa_circ_250263,RMVar_hsa_circ_250264,RMVar_hsa_circ_250265 44432 RMVar_ID_44432 Human_SNP_ID_352376268 A-to-I Human chr8 + 12449225 12449225 12449225 GTGTACACACGCATATATACATACACATGTATATGTGTGTGTGTACACACGCATATATACATATG GTGTACACACGCATATATACATACACATGTATGTGTGTGTGTGTACACACGCATATATACATATG A G lnc-ZNF705D-5,FAM66A,LOC100506990,LOC100506990:2,lnc-ZNF705D-7,LOC100506990:3,LOC100506990:4 RNACentral:URS00008B295B,RNACentral:URS00009C0E6F,RNACentral:URS00009BC63E,RNACentral:URS00008B2EB1,RNACentral:URS00008BC4CF,RNACentral:URS000075B46F,RNACentral:URS00009B808D lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron,intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1339953942 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115551,RMVar_hsa_circ_120552,RMVar_hsa_circ_250260,RMVar_hsa_circ_122929,RMVar_hsa_circ_93000,RMVar_hsa_circ_250263,RMVar_hsa_circ_250264,RMVar_hsa_circ_250265 44433 RMVar_ID_44433 Human_SNP_ID_352385762 A-to-I Human chr8 + 12479907 12479907 12479907 CTCTTGAACTCCTGACCTCAAGTGATCCACCTACCTCGGCCTCCCAAAGTGCTGGGATTACAGGT CTCTTGAACTCCTGACCTCAAGTGATCCACCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGT A G FAM66A,LOC100506990,LOC100506990:2,LOC100506990:3,LOC100506990:4 RNACentral:URS00009C0E6F,RNACentral:URS00009BC63E,RNACentral:URS00008B2EB1,RNACentral:URS000075B46F,RNACentral:URS00009B808D lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1221922779 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115551,RMVar_hsa_circ_120552,RMVar_hsa_circ_250260,RMVar_hsa_circ_122929,RMVar_hsa_circ_93000,RMVar_hsa_circ_250263,RMVar_hsa_circ_250264,RMVar_hsa_circ_250265 44434 RMVar_ID_44434 Human_SNP_ID_352396701 A-to-I Human chr8 + 12511831 12511831 12511831 AGGCGTGGCGGTACATGTCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCTTGAA AGGCGTGGCGGTACATGTCTGTAATCCCAGCTGCTCGGGAGGCTGAGGCAGGAGAATTGCTTGAA A G FAM66A,LOC100506990,LOC100506990:2,LOC100506990:3,LOC100506990:4,LOC100506990:5 RNACentral:URS00009C0E6F,RNACentral:URS00009BC63E,RNACentral:URS00008B2EB1,RNACentral:URS000075B46F,RNACentral:URS00008BC75F,RNACentral:URS00009B808D lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1198804869 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115551,RMVar_hsa_circ_120552,RMVar_hsa_circ_250260,RMVar_hsa_circ_122929,RMVar_hsa_circ_93000,RMVar_hsa_circ_250263,RMVar_hsa_circ_250264,RMVar_hsa_circ_113221,RMVar_hsa_circ_250265,RMVar_hsa_circ_250267,RMVar_hsa_circ_250269,RMVar_hsa_circ_105727 44435 RMVar_ID_44435 Human_SNP_ID_352406786 A-to-I Human chr8 + 12538705 12538705 12538705 TGTACTTAGTAGAGACAGGATTTCACCCTGTTAGCCAGGTTGGTCTTGAACTCCTGACCTCAAAT TGTACTTAGTAGAGACAGGATTTCACCCTGTTTGCCAGGTTGGTCTTGAACTCCTGACCTCAAAT A T LOC100506990,LOC100506990:2,LOC100506990:3,LOC100506990:4,LOC100506990:5,LOC100506990:6 RNACentral:URS00009BC63E,RNACentral:URS00008B2EB1,RNACentral:URS000075B46F,RNACentral:URS00008BC75F,RNACentral:URS00009BD45A,RNACentral:URS00009B808D lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1288397691 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122929,RMVar_hsa_circ_250263,RMVar_hsa_circ_250269,RMVar_hsa_circ_105727 44436 RMVar_ID_44436 Human_SNP_ID_352409537 A-to-I Human chr8 + 12545787 12545787 12545787 TGGTGAAACCCCGTGTCTACTAAAAATACAAAAAATTAGCCGGGCATGGTGGCACATGCCTGAAA TGGTGAAACCCCGTGTCTACTAAAAATACAAACAATTAGCCGGGCATGGTGGCACATGCCTGAAA A C LOC100506990,LOC100506990:2,LOC100506990:3,LOC100506990:4,LOC100506990:5,LOC100506990:6 RNACentral:URS00009BC63E,RNACentral:URS00008B2EB1,RNACentral:URS000075B46F,RNACentral:URS00008BC75F,RNACentral:URS00009BD45A,RNACentral:URS00009B808D lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs569650474 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122929,RMVar_hsa_circ_250263,RMVar_hsa_circ_250269,RMVar_hsa_circ_105727 44437 RMVar_ID_44437 Human_SNP_ID_352410077 A-to-I Human chr8 + 12547226 12547226 12547226 GAGACTGAGGCAGGAGAATGGCGTGAACGCGGAAGGTGGAGCTTGCAGTGAGCCGAGATCGCGCC GAGACTGAGGCAGGAGAATGGCGTGAACGCGGTAGGTGGAGCTTGCAGTGAGCCGAGATCGCGCC A T LOC100506990,LOC100506990:2,LOC100506990:3,LOC100506990:4,LOC100506990:5,LOC100506990:6 RNACentral:URS00009BC63E,RNACentral:URS00008B2EB1,RNACentral:URS000075B46F,RNACentral:URS00008BC75F,RNACentral:URS00009BD45A,RNACentral:URS00009B808D lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1563332698 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122929,RMVar_hsa_circ_250263,RMVar_hsa_circ_250269,RMVar_hsa_circ_105727 44438 RMVar_ID_44438 Human_SNP_ID_352410965 A-to-I Human chr8 + 12549602 12549602 12549602 CCCTGCCTCAGCCTCCTGAGTAGTGTGGGACTACAGGCGTATTCACCATGCCCGGCTAATTTTTT CCCTGCCTCAGCCTCCTGAGTAGTGTGGGACTGCAGGCGTATTCACCATGCCCGGCTAATTTTTT A G LOC100506990,LOC100506990:2,LOC100506990:3,LOC100506990:4,LOC100506990:5,LOC100506990:6 RNACentral:URS00009BC63E,RNACentral:URS00008B2EB1,RNACentral:URS000075B46F,RNACentral:URS00008BC75F,RNACentral:URS00009BD45A,RNACentral:URS00009B808D lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,exon,intron,intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1220714227 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122929,RMVar_hsa_circ_250263,RMVar_hsa_circ_250269,RMVar_hsa_circ_105727 44439 RMVar_ID_44439 Human_SNP_ID_352410966 A-to-I Human chr8 + 12549602 12549602 12549602 CCCTGCCTCAGCCTCCTGAGTAGTGTGGGACTACAGGCGTATTCACCATGCCCGGCTAATTTTTT CCCTGCCTCAGCCTCCTGAGTAGTGTGGGACTTCAGGCGTATTCACCATGCCCGGCTAATTTTTT A T LOC100506990,LOC100506990:2,LOC100506990:3,LOC100506990:4,LOC100506990:5,LOC100506990:6 RNACentral:URS00009BC63E,RNACentral:URS00008B2EB1,RNACentral:URS000075B46F,RNACentral:URS00008BC75F,RNACentral:URS00009BD45A,RNACentral:URS00009B808D lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,exon,intron,intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1220714227 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122929,RMVar_hsa_circ_250263,RMVar_hsa_circ_250269,RMVar_hsa_circ_105727 44440 RMVar_ID_44440 Human_SNP_ID_352412403 A-to-I Human chr8 + 12552672 12552672 12552672 CAAAATTTAGCTGGGCATGGTTGCACGTGCCTATAGTCCCAGCTACTCAGGAGGCTGAGGCAGGA CAAAATTTAGCTGGGCATGGTTGCACGTGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGA A G 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 GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1187954989 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_250269,RMVar_hsa_circ_105727 44441 RMVar_ID_44441 Human_SNP_ID_352412514 A-to-I Human chr8 - 12552896 12552896 12552896 ATCACACTTTGGCTTTGATTCTGGGTGGGTACAGTAGTATAGTTTGCATATGATTCCTTCAGCTG ATCACACTTTGGCTTTGATTCTGGGTGGGTACTGTAGTATAGTTTGCATATGATTCCTTCAGCTG T A AC068587.4 Ensembl:ENSG00000283674 lincRNA intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1367972173 Functional Loss SNV dbSNP153 33..33 33 - - - 44442 RMVar_ID_44442 Human_SNP_ID_352412515 A-to-I Human chr8 - 12552896 12552896 12552896 ATCACACTTTGGCTTTGATTCTGGGTGGGTACAGTAGTATAGTTTGCATATGATTCCTTCAGCTG ATCACACTTTGGCTTTGATTCTGGGTGGGTACGGTAGTATAGTTTGCATATGATTCCTTCAGCTG T C AC068587.4 Ensembl:ENSG00000283674 lincRNA intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1367972173 Functional Loss SNV dbSNP153 33..33 33 - - - 44443 RMVar_ID_44443 Human_SNP_ID_352417935 A-to-I Human chr8 + 12565650 12565622 12565650 CTGGGGAGAGAGACAGTGTAAAAGAGAGAGAGAGAGAGAGACCGTAAAAGAAGGGAGACAAAGAG CTGGG____________________________GAGAGAGACCGTAAAAGAAGGGAGACAAAGAG GGAGAGAGACAGTGTAAAAGAGAGAGAGA G 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 GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs142771663 Functional Loss DEL dbSNP153 6..33 33 - - - RMVar_hsa_circ_250269,RMVar_hsa_circ_105727 44444 RMVar_ID_44444 Human_SNP_ID_352417956 A-to-I Human chr8 + 12565650 12565650 12565650 CTGGGGAGAGAGACAGTGTAAAAGAGAGAGAGAGAGAGAGACCGTAAAAGAAGGGAGACAAAGAG CTGGGGAGAGAGACAGTGTAAAAGAGAGAGAGGGAGAGAGACCGTAAAAGAAGGGAGACAAAGAG A G 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 GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1472023670 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_250269,RMVar_hsa_circ_105727 44445 RMVar_ID_44445 Human_SNP_ID_352584946 A-to-I Human chr8 + 12962691 12962691 12962691 TTTTATATTTTTTGTAGAGACGGGGTCTCGCTATGTTGTCCAGGCTGGTCTGGAACTCCTGAGCT TTTTATATTTTTTGTAGAGACGGGGTCTCGCTGTGTTGTCCAGGCTGGTCTGGAACTCCTGAGCT A G TRMT9B Ensembl:ENSG00000250305 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs570436037 Functional Loss SNV dbSNP153 33..33 33 - - - 44446 RMVar_ID_44446 Human_SNP_ID_352585694 A-to-I Human chr8 + 12964730 12964730 12964730 CTGAGTAACTTGGACTATAAGCATGCCACCACACCAGGCTAATGTTTTTTGTTTGTTTGTTTGTT CTGAGTAACTTGGACTATAAGCATGCCACCACTCCAGGCTAATGTTTTTTGTTTGTTTGTTTGTT A T TRMT9B Ensembl:ENSG00000250305 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1411564096 Functional Loss SNV dbSNP153 33..33 33 - - - 44447 RMVar_ID_44447 Human_SNP_ID_352601493 A-to-I Human chr8 + 13006732 13006732 13006732 CTCTTGTCAACCAGATTGGAGTGCAGTGGTGCAATCTCAGCTTGCTGCAAACTCCGCCTCCCAGG CTCTTGTCAACCAGATTGGAGTGCAGTGGTGCGATCTCAGCTTGCTGCAAACTCCGCCTCCCAGG A G TRMT9B Ensembl:ENSG00000250305 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs903296710 Functional Loss SNV dbSNP153 33..33 33 - - - 44448 RMVar_ID_44448 Human_SNP_ID_352601501 A-to-I Human chr8 + 13006748 13006748 13006748 TGGAGTGCAGTGGTGCAATCTCAGCTTGCTGCAAACTCCGCCTCCCAGGTTCAACTGATTCTCCT TGGAGTGCAGTGGTGCAATCTCAGCTTGCTGCGAACTCCGCCTCCCAGGTTCAACTGATTCTCCT A G TRMT9B Ensembl:ENSG00000250305 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1001615624 Functional Loss SNV dbSNP153 33..33 33 - - - 44449 RMVar_ID_44449 Human_SNP_ID_352601527 A-to-I Human chr8 + 13006802 13006802 13006802 CTGATTCTCCTGCCTCAGACTCCCAAATAGCTATGATTACAGGCACCCGCCACCACGCCCAGCTA CTGATTCTCCTGCCTCAGACTCCCAAATAGCTGTGATTACAGGCACCCGCCACCACGCCCAGCTA A G TRMT9B Ensembl:ENSG00000250305 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs959735538 Functional Loss SNV dbSNP153 33..33 33 - - - 44450 RMVar_ID_44450 Human_SNP_ID_352601535 A-to-I Human chr8 + 13006814 13006814 13006814 CCTCAGACTCCCAAATAGCTATGATTACAGGCACCCGCCACCACGCCCAGCTAATTTTTGTATTT CCTCAGACTCCCAAATAGCTATGATTACAGGCTCCCGCCACCACGCCCAGCTAATTTTTGTATTT A T TRMT9B Ensembl:ENSG00000250305 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1394219006 Functional Loss SNV dbSNP153 33..33 33 - - - 44451 RMVar_ID_44451 Human_SNP_ID_352601572 A-to-I Human chr8 + 13006912 13006912 13006912 ACTGGTCTCAAACTCCTGACCTCAGATGATCCATCTGTCTCGGCTTCCCAAAGTGCTGGGATTAC ACTGGTCTCAAACTCCTGACCTCAGATGATCCTTCTGTCTCGGCTTCCCAAAGTGCTGGGATTAC A T TRMT9B Ensembl:ENSG00000250305 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1206534216 Functional Loss SNV dbSNP153 33..33 33 - - - 44452 RMVar_ID_44452 Human_SNP_ID_352602754 A-to-I Human chr8 + 13009860 13009860 13009860 ACAAATTACACTACAGATAGGCCAGGCGCGGTATCTCACACGTGTAATCCTAGCACTTTGGGAGG ACAAATTACACTACAGATAGGCCAGGCGCGGTGTCTCACACGTGTAATCCTAGCACTTTGGGAGG A G TRMT9B Ensembl:ENSG00000250305 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs934862431 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26152254 44453 RMVar_ID_44453 Human_SNP_ID_352602820 A-to-I Human chr8 + 13010027 13010027 13010027 TAAGCATGATACACGTGCCTGTAGTCTCAGCTACTTGGGAGGCTGAGGTAGGAGGACAGATTGAG TAAGCATGATACACGTGCCTGTAGTCTCAGCTGCTTGGGAGGCTGAGGTAGGAGGACAGATTGAG A G TRMT9B Ensembl:ENSG00000250305 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs531795746 Functional Loss SNV dbSNP153 33..33 33 - - - 44454 RMVar_ID_44454 Human_SNP_ID_352602846 A-to-I Human chr8 + 13010090 13010090 13010090 AGTCTGGGAGGCAGAGGTTGCAGTGAGCCGAGATGGTGCCACTGCATTCTAGCCTGGGTGGCATA AGTCTGGGAGGCAGAGGTTGCAGTGAGCCGAGGTGGTGCCACTGCATTCTAGCCTGGGTGGCATA A G TRMT9B Ensembl:ENSG00000250305 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1156757277 Functional Loss SNV dbSNP153 33..33 33 - - - 44455 RMVar_ID_44455 Human_SNP_ID_352602847 A-to-I Human chr8 + 13010090 13010090 13010090 AGTCTGGGAGGCAGAGGTTGCAGTGAGCCGAGATGGTGCCACTGCATTCTAGCCTGGGTGGCATA AGTCTGGGAGGCAGAGGTTGCAGTGAGCCGAGTTGGTGCCACTGCATTCTAGCCTGGGTGGCATA A T TRMT9B Ensembl:ENSG00000250305 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1156757277 Functional Loss SNV dbSNP153 33..33 33 - - - 44456 RMVar_ID_44456 Human_SNP_ID_352603204 A-to-I Human chr8 + 13011054 13011054 13011054 TCACCTAGGCTGGAGTGAGGTGATGCTACCCCAGCTCACTGCAACCTCCACCTCCTGAATTTAAG TCACCTAGGCTGGAGTGAGGTGATGCTACCCCGGCTCACTGCAACCTCCACCTCCTGAATTTAAG A G TRMT9B Ensembl:ENSG00000250305 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs913165478 Functional Loss SNV dbSNP153 33..33 33 - - - 44457 RMVar_ID_44457 Human_SNP_ID_352603205 A-to-I Human chr8 + 13011054 13011054 13011054 TCACCTAGGCTGGAGTGAGGTGATGCTACCCCAGCTCACTGCAACCTCCACCTCCTGAATTTAAG TCACCTAGGCTGGAGTGAGGTGATGCTACCCCTGCTCACTGCAACCTCCACCTCCTGAATTTAAG A T TRMT9B Ensembl:ENSG00000250305 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs913165478 Functional Loss SNV dbSNP153 33..33 33 - - - 44458 RMVar_ID_44458 Human_SNP_ID_352603237 A-to-I Human chr8 + 13011139 13011139 13011139 CTCCTGAGTAACTGGGATTACAGGTACCTGCCACCACACCCAGCTAATTTTTGTATTTTTAGTAG CTCCTGAGTAACTGGGATTACAGGTACCTGCCTCCACACCCAGCTAATTTTTGTATTTTTAGTAG A T TRMT9B Ensembl:ENSG00000250305 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs576358063 Functional Loss SNV dbSNP153 33..33 33 - - - 44459 RMVar_ID_44459 Human_SNP_ID_352603774 A-to-I Human chr8 + 13012471 13012471 13012471 GTGGCACGCGCCTATGATCCCACCTACTCGGGAGGCTAAGGCAAGAGAATTGCTTGAACCCGTGA GTGGCACGCGCCTATGATCCCACCTACTCGGGTGGCTAAGGCAAGAGAATTGCTTGAACCCGTGA A T TRMT9B Ensembl:ENSG00000250305 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs952274558 Functional Loss SNV dbSNP153 33..33 33 - - - 44460 RMVar_ID_44460 Human_SNP_ID_352605822 A-to-I Human chr8 + 13017013 13017013 13017013 GGGCATAGTAGTGCATGCCTGTAATCTCAGCTACTCAGGAGGCTGAGGTAGAAGAATTGCTTGAA GGGCATAGTAGTGCATGCCTGTAATCTCAGCTCCTCAGGAGGCTGAGGTAGAAGAATTGCTTGAA A C TRMT9B Ensembl:ENSG00000250305 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs925039815 Functional Loss SNV dbSNP153 33..33 33 - - - 44461 RMVar_ID_44461 Human_SNP_ID_352606159 A-to-I Human chr8 + 13017743 13017743 13017743 TCTAGAGATTCTCTCACATCAGTTTCCTGAGTAACTTGGACCATAGACACACACCACCACGCCCA TCTAGAGATTCTCTCACATCAGTTTCCTGAGTGACTTGGACCATAGACACACACCACCACGCCCA A G TRMT9B Ensembl:ENSG00000250305 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs987086734 Functional Loss SNV dbSNP153 33..33 33 - - - 44462 RMVar_ID_44462 Human_SNP_ID_352606160 A-to-I Human chr8 + 13017743 13017743 13017743 TCTAGAGATTCTCTCACATCAGTTTCCTGAGTAACTTGGACCATAGACACACACCACCACGCCCA TCTAGAGATTCTCTCACATCAGTTTCCTGAGTTACTTGGACCATAGACACACACCACCACGCCCA A T TRMT9B Ensembl:ENSG00000250305 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs987086734 Functional Loss SNV dbSNP153 33..33 33 - - - 44463 RMVar_ID_44463 Human_SNP_ID_352608538 A-to-I Human chr8 + 13022790 13022784 13022790 AAGGCAGAAGGATCACTTGAACCCAGGAGTTCAAGAATAGCCTGGGCAACATAGCAAGACCCCAT AAGGCAGAAGGATCACTTGAACCCAGG______AGAATAGCCTGGGCAACATAGCAAGACCCCAT GAGTTCA G TRMT9B Ensembl:ENSG00000250305 Protein coding intron GSE100210;GSE107867;GSE107867 HepG2 cell line;ASD brains,cerebellum;ASD brains,cerebellum - 29129909,30559470,30559470 RNA-Seq:(High) rs1480320233 Functional Loss DEL dbSNP153 28..33 33 - - - 44464 RMVar_ID_44464 Human_SNP_ID_352608612 A-to-I Human chr8 + 13022962 13022962 13022962 CTATGATTGCATCACTGCACTGCAGCCTGGGCAACATAGCAAGACTCTGTCTCAAAATAATAATA CTATGATTGCATCACTGCACTGCAGCCTGGGCGACATAGCAAGACTCTGTCTCAAAATAATAATA A G TRMT9B Ensembl:ENSG00000250305 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1309808032 Functional Loss SNV dbSNP153 33..33 33 - - - 44465 RMVar_ID_44465 Human_SNP_ID_352609071 A-to-I Human chr8 + 13024094 13024094 13024094 GAGACAGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCACTGGCGCGATCTCGGCTCACTGTAAGC GAGACAGAGTCTCGCTCTGTCGCCCAGGCTGGTGTGCACTGGCGCGATCTCGGCTCACTGTAAGC A T TRMT9B Ensembl:ENSG00000250305 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1370849176 Functional Loss SNV dbSNP153 33..33 33 - - - 44466 RMVar_ID_44466 Human_SNP_ID_352609107 A-to-I Human chr8 + 13024143 13024143 13024143 TCGGCTCACTGTAAGCTCCGCCTCCCGGGTTCACGCCATCCTCCTGCCTCAGCCTCCCAAGTAGC TCGGCTCACTGTAAGCTCCGCCTCCCGGGTTCGCGCCATCCTCCTGCCTCAGCCTCCCAAGTAGC A G TRMT9B Ensembl:ENSG00000250305 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1191901961 Functional Loss SNV dbSNP153 33..33 33 - - - 44467 RMVar_ID_44467 Human_SNP_ID_352636915 A-to-I Human chr8 - 13088346 13088346 13088346 GGCATATGGTGGCTCACACCTGTAATCCCAGCACTCTGGGAGGCCAAGGTGGGAGGATCACTTGA GGCATATGGTGGCTCACACCTGTAATCCCAGCGCTCTGGGAGGCCAAGGTGGGAGGATCACTTGA T C DLC1 Ensembl:ENSG00000164741 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1164733183 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91743,RMVar_hsa_circ_75979,RMVar_hsa_circ_82077,RMVar_hsa_circ_124966,RMVar_hsa_circ_250281,RMVar_hsa_circ_250282,RMVar_hsa_circ_250280,RMVar_hsa_circ_250283 44468 RMVar_ID_44468 Human_SNP_ID_352701961 A-to-I Human chr8 - 13277188 13277188 13277188 TCCCTCTCAGCCTCCCAAGCAGCTGGGACCACAGGTGCATGCCACCACACCCGCCTAATTTCTTG TCCCTCTCAGCCTCCCAAGCAGCTGGGACCACGGGTGCATGCCACCACACCCGCCTAATTTCTTG T C DLC1 Ensembl:ENSG00000164741 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1349648893 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97181,RMVar_hsa_circ_250288,RMVar_hsa_circ_122887,RMVar_hsa_circ_250291 44469 RMVar_ID_44469 Human_SNP_ID_353309088 A-to-I Human chr8 - 14879122 14879122 14879122 GGGGGTCTCACTGTGTTACTCAGGCTGGTCTTAAATTCCTGAGCTCAAGCTATCCTCCCACCTCA GGGGGTCTCACTGTGTTACTCAGGCTGGTCTTCAATTCCTGAGCTCAAGCTATCCTCCCACCTCA T G SGCZ,AC084838.1 Ensembl:ENSG00000185053,Ensembl:ENSG00000255076 Protein coding,lincRNA intron,exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs537503197 Functional Loss SNV dbSNP153 33..33 33 - - - 44470 RMVar_ID_44470 Human_SNP_ID_353309174 A-to-I Human chr8 - 14879314 14879314 14879314 TTTGTTTTGTTTTGTTTTTAACATAGAGTCTCACTCTGTCATCCAGGCTGGAGTGAGGTGGCATA TTTGTTTTGTTTTGTTTTTAACATAGAGTCTCTCTCTGTCATCCAGGCTGGAGTGAGGTGGCATA T A SGCZ,AC084838.1 Ensembl:ENSG00000185053,Ensembl:ENSG00000255076 Protein coding,lincRNA intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1434091547 Functional Loss SNV dbSNP153 33..33 33 - - - 44471 RMVar_ID_44471 Human_SNP_ID_353318507 A-to-I Human chr8 - 14907620 14907620 14907620 CCAGATTGGACTTGAACTTCTGGCCTCAAGCAACACTCCTACCTTGGCTTCCCAAAGTGCTGGGA CCAGATTGGACTTGAACTTCTGGCCTCAAGCAGCACTCCTACCTTGGCTTCCCAAAGTGCTGGGA T C SGCZ Ensembl:ENSG00000185053 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1246359629 Functional Loss SNV dbSNP153 33..33 33 - - - 44472 RMVar_ID_44472 Human_SNP_ID_286837929 A-to-I Human chr6 - 90560364 90560357 90560364 AGTGAGAGTCCGTCTCAAAAAACAAAAAGAAAAAAGAAAGTAAAAAATTAAAAGCAGGACTGATG AGTGAGAGTCCGTCTCAAAAAACAAAAAGAAA_______GTAAAAAATTAAAAGCAGGACTGATG CTTTCTTT C MAP3K7 Ensembl:ENSG00000135341 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1339231211 Functional Loss DEL dbSNP153 33..39 33 - - - Human_RBP_ID_26050635 RMVar_hsa_circ_51701,RMVar_hsa_circ_273126,RMVar_hsa_circ_240355,RMVar_hsa_circ_61431,RMVar_hsa_circ_266987,RMVar_hsa_circ_307079,RMVar_hsa_circ_240360,RMVar_hsa_circ_81136,RMVar_hsa_circ_292213,RMVar_hsa_circ_240358,RMVar_hsa_circ_19394,RMVar_hsa_circ_305091,RMVar_hsa_circ_318007,RMVar_hsa_circ_240361,RMVar_hsa_circ_312906,RMVar_hsa_circ_240362 44473 RMVar_ID_44473 Human_SNP_ID_288216161 A-to-I Human chr6 + 96069761 96069761 96069761 TCAAGCGATTCTCCAACCTCAGCCTCCCTAGTAGCCGAACTACAGGCGCGCGCCACCATGCCCAG TCAAGCGATTCTCCAACCTCAGCCTCCCTAGTGGCCGAACTACAGGCGCGCGCCACCATGCCCAG A G FUT9 Ensembl:ENSG00000172461 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1457841292 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_240379,RMVar_hsa_circ_240378 44474 RMVar_ID_44474 Human_SNP_ID_288493253 A-to-I Human chr6 - 97239656 97239656 97239656 TCCTGCCTCAGCTTCCAATAGTGCTTGGGATTACAGATGGGAGCCACCGCACCCAGCCTGACCAC TCCTGCCTCAGCTTCCAATAGTGCTTGGGATTGCAGATGGGAGCCACCGCACCCAGCCTGACCAC T C MMS22L Ensembl:ENSG00000146263 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1209542204 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15536,RMVar_hsa_circ_35131,RMVar_hsa_circ_100542,RMVar_hsa_circ_240402,RMVar_hsa_circ_104194,RMVar_hsa_circ_74944,RMVar_hsa_circ_111578,RMVar_hsa_circ_240403,RMVar_hsa_circ_240405,RMVar_hsa_circ_340780,RMVar_hsa_circ_375043,RMVar_hsa_circ_326966,RMVar_hsa_circ_49730,RMVar_hsa_circ_72640,RMVar_hsa_circ_49036,RMVar_hsa_circ_240406,RMVar_hsa_circ_46239 44475 RMVar_ID_44475 Human_SNP_ID_288497876 A-to-I Human chr6 - 97258220 97258220 97258220 TTAAGGTCTATAGGCTAAAATAGCTTTATTTTACCTCACTTTTTAAAGATATTAATAGGTAAAGA TTAAGGTCTATAGGCTAAAATAGCTTTATTTTGCCTCACTTTTTAAAGATATTAATAGGTAAAGA T C MMS22L Ensembl:ENSG00000146263 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1433813146 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4797,RMVar_hsa_circ_35131,RMVar_hsa_circ_100542,RMVar_hsa_circ_240402,RMVar_hsa_circ_104194,RMVar_hsa_circ_74944,RMVar_hsa_circ_111578,RMVar_hsa_circ_240403,RMVar_hsa_circ_240405,RMVar_hsa_circ_340780,RMVar_hsa_circ_375043,RMVar_hsa_circ_326966,RMVar_hsa_circ_49730,RMVar_hsa_circ_49036,RMVar_hsa_circ_240406,RMVar_hsa_circ_45944,RMVar_hsa_circ_46239,RMVar_hsa_circ_343631,RMVar_hsa_circ_31394,RMVar_hsa_circ_240409,RMVar_hsa_circ_53271,RMVar_hsa_circ_240408,RMVar_hsa_circ_240407,RMVar_hsa_circ_360522,RMVar_hsa_circ_377148,RMVar_hsa_circ_289971,RMVar_hsa_circ_20828 44476 RMVar_ID_44476 Human_SNP_ID_288497881 A-to-I Human chr6 - 97258231 97258231 97258231 GAGAGTCAGCCTTAAGGTCTATAGGCTAAAATAGCTTTATTTTACCTCACTTTTTAAAGATATTA GAGAGTCAGCCTTAAGGTCTATAGGCTAAAATGGCTTTATTTTACCTCACTTTTTAAAGATATTA T C MMS22L Ensembl:ENSG00000146263 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1016818439 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4797,RMVar_hsa_circ_35131,RMVar_hsa_circ_100542,RMVar_hsa_circ_240402,RMVar_hsa_circ_104194,RMVar_hsa_circ_74944,RMVar_hsa_circ_111578,RMVar_hsa_circ_240403,RMVar_hsa_circ_240405,RMVar_hsa_circ_340780,RMVar_hsa_circ_375043,RMVar_hsa_circ_326966,RMVar_hsa_circ_49730,RMVar_hsa_circ_49036,RMVar_hsa_circ_240406,RMVar_hsa_circ_45944,RMVar_hsa_circ_46239,RMVar_hsa_circ_343631,RMVar_hsa_circ_31394,RMVar_hsa_circ_240409,RMVar_hsa_circ_53271,RMVar_hsa_circ_240408,RMVar_hsa_circ_240407,RMVar_hsa_circ_360522,RMVar_hsa_circ_377148,RMVar_hsa_circ_289971,RMVar_hsa_circ_20828 44477 RMVar_ID_44477 Human_SNP_ID_288882570 A-to-I Human chr6 - 98869469 98869469 98869469 ACCACCACACCTGGCTAATTTTTTTATTTTTTATAGAGACACAGTCTTTCCATGTTGCCTATGTT ACCACCACACCTGGCTAATTTTTTTATTTTTTGTAGAGACACAGTCTTTCCATGTTGCCTATGTT T C FBXL4 Ensembl:ENSG00000112234 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs999444337 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15918104 44478 RMVar_ID_44478 Human_SNP_ID_288883553 A-to-I Human chr6 - 98873724 98873724 98873724 TTTTCTAGCCAGGTGTGGTGGCACACACTTGTAGTCCTAGCGACACAGGAGGTGGAGGCAGGAGG TTTTCTAGCCAGGTGTGGTGGCACACACTTGTGGTCCTAGCGACACAGGAGGTGGAGGCAGGAGG T C FBXL4 Ensembl:ENSG00000112234 Protein coding 3'UTR GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1186064849 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24178173 44479 RMVar_ID_44479 Human_SNP_ID_288895638 A-to-I Human chr6 - 98924435 98924435 98924435 CTCCTGCCTCAGCCACCTGAGCGGCTGGGATTACAGGTGCGTGCCACCATGCCTGGCTAATTTTT CTCCTGCCTCAGCCACCTGAGCGGCTGGGATTGCAGGTGCGTGCCACCATGCCTGGCTAATTTTT T C FBXL4 Ensembl:ENSG00000112234 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1341041989 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_278789,RMVar_hsa_circ_302317,RMVar_hsa_circ_265307,RMVar_hsa_circ_278739,RMVar_hsa_circ_240463,RMVar_hsa_circ_240464,RMVar_hsa_circ_312518,RMVar_hsa_circ_240468,RMVar_hsa_circ_240467,RMVar_hsa_circ_240469,RMVar_hsa_circ_273240,RMVar_hsa_circ_377839,RMVar_hsa_circ_288383,RMVar_hsa_circ_240470,RMVar_hsa_circ_240473,RMVar_hsa_circ_113577,RMVar_hsa_circ_315787,RMVar_hsa_circ_337110,RMVar_hsa_circ_14869,RMVar_hsa_circ_7521,RMVar_hsa_circ_240475,RMVar_hsa_circ_49962 44480 RMVar_ID_44480 Human_SNP_ID_288898445 A-to-I Human chr6 - 98936729 98936729 98936729 AACTACCACTGAATAGCCTATGGTTGACTGGAAGCCTTACTGATAACATATACAGTTGGTTAATA AACTACCACTGAATAGCCTATGGTTGACTGGACGCCTTACTGATAACATATACAGTTGGTTAATA T G FBXL4 Ensembl:ENSG00000112234 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs959510336 Functional Loss SNV dbSNP153 33..33 33 - - - 44481 RMVar_ID_44481 Human_SNP_ID_289010771 A-to-I Human chr6 - 99405302 99405302 99405302 CCACCATGCCTGGCTAATTTTTGTATTTTTTCAGTAGAGACAAGGTTTCGCCATGTTGTTCAGGC CCACCATGCCTGGCTAATTTTTGTATTTTTTCGGTAGAGACAAGGTTTCGCCATGTTGTTCAGGC T C PNISR Ensembl:ENSG00000132424 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1029923030 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10742,RMVar_hsa_circ_240487,RMVar_hsa_circ_58475,RMVar_hsa_circ_355164,RMVar_hsa_circ_364170,RMVar_hsa_circ_364336,RMVar_hsa_circ_363143,RMVar_hsa_circ_126115,RMVar_hsa_circ_240488,RMVar_hsa_circ_240489 44482 RMVar_ID_44482 Human_SNP_ID_289012625 A-to-I Human chr6 - 99412500 99412500 99412500 CACAATTTTAAGACTTTTAAAAAACAGAATGAAGATTATTATTAAATTTTTTAATTTGCTTAGTT CACAATTTTAAGACTTTTAAAAAACAGAATGAGGATTATTATTAAATTTTTTAATTTGCTTAGTT T C PNISR Ensembl:ENSG00000132424 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1168642479 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2031480,Human_RBP_ID_7651392,Human_RBP_ID_10308565,Human_RBP_ID_23067187,Human_RBP_ID_24513708,Human_RBP_ID_26037194,Human_RBP_ID_26719657 RMVar_hsa_circ_8401,RMVar_hsa_circ_355164,RMVar_hsa_circ_363143,RMVar_hsa_circ_126115,RMVar_hsa_circ_240488,RMVar_hsa_circ_240489,RMVar_hsa_circ_68467,RMVar_hsa_circ_365877,RMVar_hsa_circ_278278,RMVar_hsa_circ_240490 44483 RMVar_ID_44483 Human_SNP_ID_289014173 A-to-I Human chr6 - 99418411 99418411 99418411 AAAGCTTCAGCTGGGTGCGGTGGTTCACACCTATAATCCCAGCACTTTGGGAGGCTGAGGTGGGT AAAGCTTCAGCTGGGTGCGGTGGTTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGT T C PNISR Ensembl:ENSG00000132424 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1209577008 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15919890,Human_RBP_ID_26037291 44484 RMVar_ID_44484 Human_SNP_ID_289014326 A-to-I Human chr6 - 99419064 99419064 99419064 CTCACTGCGACTTCCACCTCCCGGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCGGAGTAGCTGGG CTCACTGCGACTTCCACCTCCCGGGTTCAAGCCGTTCTCCTGCCTCAGCCTCCGGAGTAGCTGGG T G PNISR Ensembl:ENSG00000132424 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1310019743 Functional Loss SNV dbSNP153 33..33 33 - - - 44485 RMVar_ID_44485 Human_SNP_ID_289014657 A-to-I Human chr6 - 99420149 99420149 99420149 GGCCGGGAGCGATAGCTCACGTCTGTAATCCCAGCACTTTGGGGACTGAGGCGGGAGGATCACGA GGCCGGGAGCGATAGCTCACGTCTGTAATCCCCGCACTTTGGGGACTGAGGCGGGAGGATCACGA T G PNISR Ensembl:ENSG00000132424 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs564512444 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7651512 44486 RMVar_ID_44486 Human_SNP_ID_289014665 A-to-I Human chr6 - 99420168 99420168 99420168 TTTTAAGAATGCAGTTATGGGCCGGGAGCGATAGCTCACGTCTGTAATCCCAGCACTTTGGGGAC TTTTAAGAATGCAGTTATGGGCCGGGAGCGATGGCTCACGTCTGTAATCCCAGCACTTTGGGGAC T C PNISR Ensembl:ENSG00000132424 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1334733803 Functional Loss SNV dbSNP153 33..33 33 - - - 44487 RMVar_ID_44487 Human_SNP_ID_289015039 A-to-I Human chr6 - 99421732 99421732 99421732 GTTTTCTAGGGATATTGTAGCAAATTACCACAAACTGGCTGATTTCAAACAACAGAAATTTATTC GTTTTCTAGGGATATTGTAGCAAATTACCACATACTGGCTGATTTCAAACAACAGAAATTTATTC T A PNISR Ensembl:ENSG00000132424 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs936858917 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15920005 44488 RMVar_ID_44488 Human_SNP_ID_289016741 A-to-I Human chr6 + 99428034 99428034 99428034 GGCCACCATGGGGAAACTGCCTACAAAAAAATACAAAAATTAGCTGGGTGTGGTGGCCCAGCTAC GGCCACCATGGGGAAACTGCCTACAAAAAAATTCAAAAATTAGCTGGGTGTGGTGGCCCAGCTAC A T AL513550.1 Ensembl:ENSG00000228506 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1182993646 Functional Loss SNV dbSNP153 33..33 33 - - - 44489 RMVar_ID_44489 Human_SNP_ID_289017025 A-to-I Human chr6 + 99429112 99429112 99429112 TGACCTCATGATCTGCCCACTTCAGCCTCTCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCAC TGACCTCATGATCTGCCCACTTCAGCCTCTCAGAGTGCTGGGATTACAGGTGTGAGCCACCGCAC A G AL513550.1 Ensembl:ENSG00000228506 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1346782204 Functional Loss SNV dbSNP153 33..33 33 - - - 44490 RMVar_ID_44490 Human_SNP_ID_289020498 A-to-I Human chr6 - 99444214 99444214 99444214 AGCCAGGAGTTCAAGACCAGTCTGAGGAACATAGTGAGATCCCATGTCTACAAAAAACGTTTTAA AGCCAGGAGTTCAAGACCAGTCTGAGGAACATGGTGAGATCCCATGTCTACAAAAAACGTTTTAA T C USP45 Ensembl:ENSG00000123552 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1236919065 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39989,RMVar_hsa_circ_240494,RMVar_hsa_circ_269289,RMVar_hsa_circ_65370,RMVar_hsa_circ_344511,RMVar_hsa_circ_348845,RMVar_hsa_circ_67908,RMVar_hsa_circ_48004,RMVar_hsa_circ_63828,RMVar_hsa_circ_50747,RMVar_hsa_circ_70942,RMVar_hsa_circ_272726,RMVar_hsa_circ_314943,RMVar_hsa_circ_374021,RMVar_hsa_circ_52163,RMVar_hsa_circ_240496,RMVar_hsa_circ_240497,RMVar_hsa_circ_355747,RMVar_hsa_circ_240495,RMVar_hsa_circ_337654,RMVar_hsa_circ_61302 44491 RMVar_ID_44491 Human_SNP_ID_289020513 A-to-I Human chr6 - 99444304 99444304 99444304 ATCTTAGGAATTTAGAAATTGGGGCTGGGCACAGTGGCTTACACCTGTAATCCCAACACTTTGGG ATCTTAGGAATTTAGAAATTGGGGCTGGGCACCGTGGCTTACACCTGTAATCCCAACACTTTGGG T G USP45 Ensembl:ENSG00000123552 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1562303630 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39989,RMVar_hsa_circ_240494,RMVar_hsa_circ_269289,RMVar_hsa_circ_65370,RMVar_hsa_circ_344511,RMVar_hsa_circ_348845,RMVar_hsa_circ_67908,RMVar_hsa_circ_48004,RMVar_hsa_circ_63828,RMVar_hsa_circ_50747,RMVar_hsa_circ_70942,RMVar_hsa_circ_272726,RMVar_hsa_circ_314943,RMVar_hsa_circ_374021,RMVar_hsa_circ_52163,RMVar_hsa_circ_240496,RMVar_hsa_circ_240497,RMVar_hsa_circ_355747,RMVar_hsa_circ_240495,RMVar_hsa_circ_337654,RMVar_hsa_circ_61302 44492 RMVar_ID_44492 Human_SNP_ID_289023607 A-to-I Human chr6 + 99456012 99456012 99456012 AAAATTAACCGGGCTTGATGGCGGGCACCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA AAAATTAACCGGGCTTGATGGCGGGCACCTGTGGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1445391455 Functional Loss SNV dbSNP153 33..33 33 - - - 44493 RMVar_ID_44493 Human_SNP_ID_289030555 A-to-I Human chr6 - 99484700 99484700 99484700 TGCAGCCTGGGCTTAAGGGATCCTCCCACTTCAGCCTCCTGAGTAGCTCGGACTGCAGGCACGTG TGCAGCCTGGGCTTAAGGGATCCTCCCACTTCGGCCTCCTGAGTAGCTCGGACTGCAGGCACGTG T C USP45 Ensembl:ENSG00000123552 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1031432837 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_240494,RMVar_hsa_circ_269289,RMVar_hsa_circ_348845,RMVar_hsa_circ_6653,RMVar_hsa_circ_63828,RMVar_hsa_circ_314943,RMVar_hsa_circ_240495,RMVar_hsa_circ_240500,RMVar_hsa_circ_360859,RMVar_hsa_circ_348248,RMVar_hsa_circ_287540,RMVar_hsa_circ_268630,RMVar_hsa_circ_240501,RMVar_hsa_circ_267188,RMVar_hsa_circ_370719,RMVar_hsa_circ_298264,RMVar_hsa_circ_364460,RMVar_hsa_circ_240504,RMVar_hsa_circ_240505,RMVar_hsa_circ_319495,RMVar_hsa_circ_366575 44494 RMVar_ID_44494 Human_SNP_ID_289039513 A-to-I Human chr6 + 99521991 99521991 99521991 GGCTCAAGCGATCCTCCCCTCAGTCTGCACGTAGCTAGGACTACAGGCGGAGGCCATCAGGCCCA GGCTCAAGCGATCCTCCCCTCAGTCTGCACGTGGCTAGGACTACAGGCGGAGGCCATCAGGCCCA A G TSTD3 Ensembl:ENSG00000279170 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs773985143 Functional Loss SNV dbSNP153 33..33 33 - - - 44495 RMVar_ID_44495 Human_SNP_ID_289039515 A-to-I Human chr6 + 99521995 99521993 99521995 CAAGCGATCCTCCCCTCAGTCTGCACGTAGCTAGGACTACAGGCGGAGGCCATCAGGCCCAGCTG CAAGCGATCCTCCCCTCAGTCTGCACGTAGC__GGACTACAGGCGGAGGCCATCAGGCCCAGCTG CTA C TSTD3 Ensembl:ENSG00000279170 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1426970928 Functional Loss DEL dbSNP153 32..33 33 - - - 44496 RMVar_ID_44496 Human_SNP_ID_289041784 A-to-I Human chr6 + 99532035 99532035 99532035 CCGAGGCAGGTGGATCACGAGGTCAGGAGATCAAGACCACCCTGGCCAACATGGTGAAACCCTGT CCGAGGCAGGTGGATCACGAGGTCAGGAGATCGAGACCACCCTGGCCAACATGGTGAAACCCTGT A G TSTD3 Ensembl:ENSG00000279170 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs765310941 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82600,RMVar_hsa_circ_104653,RMVar_hsa_circ_240510,RMVar_hsa_circ_240512,RMVar_hsa_circ_101074,RMVar_hsa_circ_240511 44497 RMVar_ID_44497 Human_SNP_ID_289041804 A-to-I Human chr6 + 99532138 99532138 99532138 ACACTCCTGTAGTCCCAGCTACTTGGAAGGCTAAGGCAGGAGAATCGCTTGAACCTGGGAAGCGG ACACTCCTGTAGTCCCAGCTACTTGGAAGGCTGAGGCAGGAGAATCGCTTGAACCTGGGAAGCGG A G TSTD3 Ensembl:ENSG00000279170 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs144589152 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82600,RMVar_hsa_circ_104653,RMVar_hsa_circ_240510,RMVar_hsa_circ_240512,RMVar_hsa_circ_101074,RMVar_hsa_circ_240511 44498 RMVar_ID_44498 Human_SNP_ID_289041964 A-to-I Human chr6 + 99532999 99532999 99532999 CCAACATGGTGAAACCACCCCCCGTCTCTACTAAAATACAAAAAATCAGCCAGGCATGGTGGCGG CCAACATGGTGAAACCACCCCCCGTCTCTACTGAAATACAAAAAATCAGCCAGGCATGGTGGCGG A G TSTD3 Ensembl:ENSG00000279170 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1199371328 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82600,RMVar_hsa_circ_104653,RMVar_hsa_circ_240510,RMVar_hsa_circ_240512,RMVar_hsa_circ_101074,RMVar_hsa_circ_240511 44499 RMVar_ID_44499 Human_SNP_ID_289042080 A-to-I Human chr6 + 99533326 99533326 99533326 TAATCCCAGAACTTTGGGATGCCTAGGCAGGCAGATCGCTTGAGCTCAGGAGTTCAAGACCAACC TAATCCCAGAACTTTGGGATGCCTAGGCAGGCTGATCGCTTGAGCTCAGGAGTTCAAGACCAACC A T TSTD3 Ensembl:ENSG00000279170 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs551498657 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104653,RMVar_hsa_circ_240512 44500 RMVar_ID_44500 Human_SNP_ID_289042482 A-to-I Human chr6 + 99535261 99535261 99535261 ACAGCTCATTGCAACCTATACCTCCTGGGCTGAAGCAATCCTCCCACCTCAGCCTCCAGAATAGC ACAGCTCATTGCAACCTATACCTCCTGGGCTGGAGCAATCCTCCCACCTCAGCCTCCAGAATAGC A G TSTD3 Ensembl:ENSG00000279170 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005969247 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104653,RMVar_hsa_circ_240512 44501 RMVar_ID_44501 Human_SNP_ID_289042910 A-to-I Human chr6 + 99536441 99536441 99536441 TCTTTTTTTTTTTTTTTTTAAGACAGGGTCTCACTCTGTCTCCTGGCTGGAGTGCAGTGGCATGA TCTTTTTTTTTTTTTTTTTAAGACAGGGTCTCTCTCTGTCTCCTGGCTGGAGTGCAGTGGCATGA A T TSTD3 Ensembl:ENSG00000279170 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1468022383 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15944908 RMVar_hsa_circ_104653,RMVar_hsa_circ_240512 44502 RMVar_ID_44502 Human_SNP_ID_289042948 A-to-I Human chr6 + 99536598 99536598 99536598 TTTTGTAGAAGTGGGGTTTCACCATGTTTCCCAGGCTGGTCTCAAACTCCTGGGTTCAAGTAATC TTTTGTAGAAGTGGGGTTTCACCATGTTTCCCCGGCTGGTCTCAAACTCCTGGGTTCAAGTAATC A C TSTD3 Ensembl:ENSG00000279170 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1382160893 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104653,RMVar_hsa_circ_240512 44503 RMVar_ID_44503 Human_SNP_ID_289042951 A-to-I Human chr6 + 99536627 99536627 99536627 CCCAGGCTGGTCTCAAACTCCTGGGTTCAAGTAATCACCCTGCCTTGGCCTCCCAAAGTGTTGGG CCCAGGCTGGTCTCAAACTCCTGGGTTCAAGTGATCACCCTGCCTTGGCCTCCCAAAGTGTTGGG A G TSTD3 Ensembl:ENSG00000279170 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1306626633 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104653,RMVar_hsa_circ_240512 44504 RMVar_ID_44504 Human_SNP_ID_289043523 A-to-I Human chr6 + 99539163 99539163 99539163 GAGACCAGCCTGGAAAACACAGTGAGACCTCTATTTCCACAAAAAATTTAAAAATTAGCTGTGCA GAGACCAGCCTGGAAAACACAGTGAGACCTCTTTTTCCACAAAAAATTTAAAAATTAGCTGTGCA A T TSTD3 Ensembl:ENSG00000279170 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1174717384 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104653,RMVar_hsa_circ_240512 44505 RMVar_ID_44505 Human_SNP_ID_289043791 A-to-I Human chr6 + 99540440 99540440 99540440 AGTCTCATTCCATTATCCAGGCTGCCCAGGCTAGAGTGCAGTGGCATGATCTCAGCTCACCACAG AGTCTCATTCCATTATCCAGGCTGCCCAGGCTGGAGTGCAGTGGCATGATCTCAGCTCACCACAG A G TSTD3 Ensembl:ENSG00000279170 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1012463059 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104653,RMVar_hsa_circ_240512 44506 RMVar_ID_44506 Human_SNP_ID_289044010 A-to-I Human chr6 + 99541458 99541458 99541458 CAGCCTGGCTAACATGGCGAAGCCCTGTCTCTAATAAAAATACAAAAAATTAGCCAGGCGTGGTG CAGCCTGGCTAACATGGCGAAGCCCTGTCTCTGATAAAAATACAAAAAATTAGCCAGGCGTGGTG A G TSTD3 Ensembl:ENSG00000279170 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1190226902 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104653,RMVar_hsa_circ_240512 44507 RMVar_ID_44507 Human_SNP_ID_289047048 A-to-I Human chr6 - 99555530 99555530 99555530 ACTAGGCTGAAGTGGGAGGGTTGCCTAAGCCCAGGAGTTCAAGGCTGCAGTAAACTGTGATTATG ACTAGGCTGAAGTGGGAGGGTTGCCTAAGCCCGGGAGTTCAAGGCTGCAGTAAACTGTGATTATG T C CCNC Ensembl:ENSG00000112237 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1472742109 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34058,RMVar_hsa_circ_83890,RMVar_hsa_circ_240513,RMVar_hsa_circ_357178,RMVar_hsa_circ_330093,RMVar_hsa_circ_309821,RMVar_hsa_circ_11549,RMVar_hsa_circ_304739,RMVar_hsa_circ_240516,RMVar_hsa_circ_240517,RMVar_hsa_circ_18805,RMVar_hsa_circ_334908,RMVar_hsa_circ_240518,RMVar_hsa_circ_321563,RMVar_hsa_circ_102422,RMVar_hsa_circ_240519,RMVar_hsa_circ_240520 44508 RMVar_ID_44508 Human_SNP_ID_289047052 A-to-I Human chr6 - 99555535 99555535 99555535 ACTCAACTAGGCTGAAGTGGGAGGGTTGCCTAAGCCCAGGAGTTCAAGGCTGCAGTAAACTGTGA ACTCAACTAGGCTGAAGTGGGAGGGTTGCCTACGCCCAGGAGTTCAAGGCTGCAGTAAACTGTGA T G CCNC Ensembl:ENSG00000112237 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs745994479 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34058,RMVar_hsa_circ_83890,RMVar_hsa_circ_240513,RMVar_hsa_circ_357178,RMVar_hsa_circ_330093,RMVar_hsa_circ_309821,RMVar_hsa_circ_11549,RMVar_hsa_circ_304739,RMVar_hsa_circ_240516,RMVar_hsa_circ_240517,RMVar_hsa_circ_18805,RMVar_hsa_circ_334908,RMVar_hsa_circ_240518,RMVar_hsa_circ_321563,RMVar_hsa_circ_102422,RMVar_hsa_circ_240519,RMVar_hsa_circ_240520 44509 RMVar_ID_44509 Human_SNP_ID_289047061 A-to-I Human chr6 + 99555572 99555572 99555572 CAACCCTCCCACTTCAGCCTAGTTGAGTAGCTAGGACTACAGGTGTGTGCCACCATGCCCAGTTA CAACCCTCCCACTTCAGCCTAGTTGAGTAGCTTGGACTACAGGTGTGTGCCACCATGCCCAGTTA A T TSTD3 Ensembl:ENSG00000279170 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs945844487 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104653,RMVar_hsa_circ_240512 44510 RMVar_ID_44510 Human_SNP_ID_289047065 A-to-I Human chr6 - 99555595 99555595 99555595 TCTGCAAAAAATTAAAGAAAAACTAACTGGGCATGGTGGCACACACCTGTAGTCCTAGCTACTCA TCTGCAAAAAATTAAAGAAAAACTAACTGGGCTTGGTGGCACACACCTGTAGTCCTAGCTACTCA T A CCNC Ensembl:ENSG00000112237 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432868677 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34058,RMVar_hsa_circ_83890,RMVar_hsa_circ_240513,RMVar_hsa_circ_357178,RMVar_hsa_circ_330093,RMVar_hsa_circ_309821,RMVar_hsa_circ_11549,RMVar_hsa_circ_304739,RMVar_hsa_circ_240516,RMVar_hsa_circ_240517,RMVar_hsa_circ_18805,RMVar_hsa_circ_334908,RMVar_hsa_circ_240518,RMVar_hsa_circ_321563,RMVar_hsa_circ_102422,RMVar_hsa_circ_240519,RMVar_hsa_circ_240520 44511 RMVar_ID_44511 Human_SNP_ID_289052050 A-to-I Human chr6 + 99576423 99576423 99576423 ATCTCAGAAGAGAAGGGTAGGAAGCCAGAGCCACCTGCCATGTCCCAGCCAGTCCCCACAGCATA ATCTCAGAAGAGAAGGGTAGGAAGCCAGAGCCCCCTGCCATGTCCCAGCCAGTCCCCACAGCATA A C TSTD3,AL137784.1 Ensembl:ENSG00000279170,Ensembl:ENSG00000219755 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025178804 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1851133,Human_miRNA_ID_1900341,Human_miRNA_ID_1908336,Human_miRNA_ID_2331024,Human_miRNA_ID_2964106,Human_miRNA_ID_3068506 RMVar_hsa_circ_104653,RMVar_hsa_circ_240512 44512 RMVar_ID_44512 Human_SNP_ID_289355926 A-to-I Human chr6 - 100821157 100821157 100821157 ATAATTAGCTGAGTGTGTTCGTTTGCACCTATAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGC ATAATTAGCTGAGTGTGTTCGTTTGCACCTATGGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGC T C ASCC3 Ensembl:ENSG00000112249 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1366207964 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117155,RMVar_hsa_circ_240529,RMVar_hsa_circ_114243,RMVar_hsa_circ_91287,RMVar_hsa_circ_240542,RMVar_hsa_circ_240543,RMVar_hsa_circ_117329,RMVar_hsa_circ_240553,RMVar_hsa_circ_102512,RMVar_hsa_circ_240562,RMVar_hsa_circ_13275,RMVar_hsa_circ_240581,RMVar_hsa_circ_288814,RMVar_hsa_circ_307280,RMVar_hsa_circ_240580,RMVar_hsa_circ_357001,RMVar_hsa_circ_9025,RMVar_hsa_circ_363990,RMVar_hsa_circ_276119,RMVar_hsa_circ_240595,RMVar_hsa_circ_318511,RMVar_hsa_circ_287159,RMVar_hsa_circ_240596,RMVar_hsa_circ_73556,RMVar_hsa_circ_303993,RMVar_hsa_circ_26493 44513 RMVar_ID_44513 Human_SNP_ID_289355927 A-to-I Human chr6 - 100821159 100821159 100821159 AAATAATTAGCTGAGTGTGTTCGTTTGCACCTATAGTCCCAGCTACTTGGGAGGCTGAGGCAGGA AAATAATTAGCTGAGTGTGTTCGTTTGCACCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGA T C ASCC3 Ensembl:ENSG00000112249 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs566141963 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117155,RMVar_hsa_circ_240529,RMVar_hsa_circ_114243,RMVar_hsa_circ_91287,RMVar_hsa_circ_240542,RMVar_hsa_circ_240543,RMVar_hsa_circ_117329,RMVar_hsa_circ_240553,RMVar_hsa_circ_102512,RMVar_hsa_circ_240562,RMVar_hsa_circ_13275,RMVar_hsa_circ_240581,RMVar_hsa_circ_288814,RMVar_hsa_circ_307280,RMVar_hsa_circ_240580,RMVar_hsa_circ_357001,RMVar_hsa_circ_9025,RMVar_hsa_circ_363990,RMVar_hsa_circ_276119,RMVar_hsa_circ_240595,RMVar_hsa_circ_318511,RMVar_hsa_circ_287159,RMVar_hsa_circ_240596,RMVar_hsa_circ_73556,RMVar_hsa_circ_303993,RMVar_hsa_circ_26493 44514 RMVar_ID_44514 Human_SNP_ID_289361167 A-to-I Human chr6 - 100842915 100842915 100842915 GCTGGAGTGTAGTGGCATGATCATAGTTTACTATAACCTGTAACTCCTGGGCTCAAGCAATCCTC GCTGGAGTGTAGTGGCATGATCATAGTTTACTGTAACCTGTAACTCCTGGGCTCAAGCAATCCTC T C ASCC3 Ensembl:ENSG00000112249 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1002815387 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15578588 RMVar_hsa_circ_117155,RMVar_hsa_circ_240529,RMVar_hsa_circ_114243,RMVar_hsa_circ_91287,RMVar_hsa_circ_240542,RMVar_hsa_circ_240543,RMVar_hsa_circ_117329,RMVar_hsa_circ_240553,RMVar_hsa_circ_102512,RMVar_hsa_circ_240562,RMVar_hsa_circ_13275,RMVar_hsa_circ_240581,RMVar_hsa_circ_288814,RMVar_hsa_circ_307280,RMVar_hsa_circ_240580,RMVar_hsa_circ_357001,RMVar_hsa_circ_9025,RMVar_hsa_circ_363990,RMVar_hsa_circ_276119,RMVar_hsa_circ_240595,RMVar_hsa_circ_318511,RMVar_hsa_circ_287159,RMVar_hsa_circ_240596,RMVar_hsa_circ_73556,RMVar_hsa_circ_303993,RMVar_hsa_circ_26493 44515 RMVar_ID_44515 Human_SNP_ID_289519146 A-to-I Human chr6 + 101496887 101496887 101496887 TGATCAAATAAACCTTTGGAATAGTTTTTATCATGGTTTGAGAAATAACGTTGTTGCTTGATGAC TGATCAAATAAACCTTTGGAATAGTTTTTATCGTGGTTTGAGAAATAACGTTGTTGCTTGATGAC A G GRIK2 Ensembl:ENSG00000164418 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1165297891 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18887 44516 RMVar_ID_44516 Human_SNP_ID_289644976 A-to-I Human chr6 + 101990929 101990929 101990929 GTTGCTTCATTTCAATAGTAAAGGTGCATACTAAATGCCTTATTACAAGTAAATAATAAATTACA GTTGCTTCATTTCAATAGTAAAGGTGCATACTGAATGCCTTATTACAAGTAAATAATAAATTACA A G GRIK2 Ensembl:ENSG00000164418 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1208772433 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_345642,RMVar_hsa_circ_14193,RMVar_hsa_circ_290771,RMVar_hsa_circ_268476,RMVar_hsa_circ_240621,RMVar_hsa_circ_329434,RMVar_hsa_circ_377526 44517 RMVar_ID_44517 Human_SNP_ID_289645048 A-to-I Human chr6 + 101991183 101991183 101991183 TAATGCTAGTGAGTCTCAATCACACAATGATTATTAATTTCACTCTTTATTGAGACTTTATCGTA TAATGCTAGTGAGTCTCAATCACACAATGATTTTTAATTTCACTCTTTATTGAGACTTTATCGTA A T GRIK2 Ensembl:ENSG00000164418 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1046242726 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_345642,RMVar_hsa_circ_14193,RMVar_hsa_circ_290771,RMVar_hsa_circ_268476,RMVar_hsa_circ_240621,RMVar_hsa_circ_329434,RMVar_hsa_circ_377526 44518 RMVar_ID_44518 Human_SNP_ID_290161812 A-to-I Human chr6 - 104018049 104018042 104018049 CCTCCCTTGCTGCATGACCAGTCAACTTACACAGTACACCAGGGACAGAGTGGACTGAAGCATGA CCTCCCTTGCTGCATGACCAGTCAACTTACAC_______CAGGGACAGAGTGGACTGAAGCATGA GGTGTACT G R3HDM2P2 Ensembl:ENSG00000216817 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs534702391 Functional Loss DEL dbSNP153 33..39 33 - - - 44519 RMVar_ID_44519 Human_SNP_ID_290161817 A-to-I Human chr6 - 104018065 104018064 104018065 TAATCTGTCCATCTGCCCTCCCTTGCTGCATGACCAGTCAACTTACACAGTACACCAGGGACAGA TAATCTGTCCATCTGCCCTCCCTTGCTGCATG_CCAGTCAACTTACACAGTACACCAGGGACAGA GT G R3HDM2P2 Ensembl:ENSG00000216817 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444088836 Functional Loss DEL dbSNP153 33..33 33 - - - 44520 RMVar_ID_44520 Human_SNP_ID_290346107 A-to-I Human chr6 - 104777892 104777891 104777892 AGCCAGGCGTGGTGGTGCGTGCCTGCAATCCCAGCTACTTGAGAGGCTGAGGCAGGAGAATCACT AGCCAGGCGTGGTGGTGCGTGCCTGCAATCCC_GCTACTTGAGAGGCTGAGGCAGGAGAATCACT CT C HACE1 Ensembl:ENSG00000085382 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1343386898 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_43002,RMVar_hsa_circ_329088,RMVar_hsa_circ_333979,RMVar_hsa_circ_367081,RMVar_hsa_circ_344341,RMVar_hsa_circ_317543,RMVar_hsa_circ_240629,RMVar_hsa_circ_240630,RMVar_hsa_circ_90005,RMVar_hsa_circ_240628,RMVar_hsa_circ_80432,RMVar_hsa_circ_330480,RMVar_hsa_circ_240635,RMVar_hsa_circ_240636,RMVar_hsa_circ_346705,RMVar_hsa_circ_350240,RMVar_hsa_circ_339392,RMVar_hsa_circ_325269,RMVar_hsa_circ_327388,RMVar_hsa_circ_19623,RMVar_hsa_circ_240639,RMVar_hsa_circ_240640,RMVar_hsa_circ_240638,RMVar_hsa_circ_367122 44521 RMVar_ID_44521 Human_SNP_ID_290361695 A-to-I Human chr6 - 104842949 104842949 104842949 CGCCACCATGTCCAGATAATTTTTATGTTTTTAGTAGAGGTGGGGTTTCACCATGTTGGCCAGGC CGCCACCATGTCCAGATAATTTTTATGTTTTTGGTAGAGGTGGGGTTTCACCATGTTGGCCAGGC T C AL357315.1,HACE1 Ensembl:ENSG00000227535,Ensembl:ENSG00000085382 lincRNA,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1226760109 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_344341,RMVar_hsa_circ_90005,RMVar_hsa_circ_36352,RMVar_hsa_circ_240636,RMVar_hsa_circ_346705,RMVar_hsa_circ_339392,RMVar_hsa_circ_240643,RMVar_hsa_circ_30032,RMVar_hsa_circ_11478,RMVar_hsa_circ_74556,RMVar_hsa_circ_300943,RMVar_hsa_circ_240649,RMVar_hsa_circ_320726,RMVar_hsa_circ_326988,RMVar_hsa_circ_3721,RMVar_hsa_circ_240655,RMVar_hsa_circ_112520,RMVar_hsa_circ_240650,RMVar_hsa_circ_240651,RMVar_hsa_circ_101656,RMVar_hsa_circ_240653,RMVar_hsa_circ_281042,RMVar_hsa_circ_301068,RMVar_hsa_circ_337044,RMVar_hsa_circ_240657,RMVar_hsa_circ_240656,RMVar_hsa_circ_240661,RMVar_hsa_circ_285049,RMVar_hsa_circ_299202,RMVar_hsa_circ_240654,RMVar_hsa_circ_290970,RMVar_hsa_circ_276105,RMVar_hsa_circ_240663,RMVar_hsa_circ_80374,RMVar_hsa_circ_240664,RMVar_hsa_circ_240662,RMVar_hsa_circ_240660,RMVar_hsa_circ_240665 44522 RMVar_ID_44522 Human_SNP_ID_467600256 A-to-I Human chr11 - 56205375 56205375 56205375 CATCATGACACTTGGATATCTGGCACCTTACCAAAGGCTAGGAATAGGAACTACAATGTTAATTC CATCATGACACTTGGATATCTGGCACCTTACCGAAGGCTAGGAATAGGAACTACAATGTTAATTC T C AC022882.1 Ensembl:ENSG00000213604 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1338494521 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1869692,Human_miRNA_ID_1911428 44523 RMVar_ID_44523 Human_SNP_ID_467600257 A-to-I Human chr11 - 56205375 56205375 56205375 CATCATGACACTTGGATATCTGGCACCTTACCAAAGGCTAGGAATAGGAACTACAATGTTAATTC CATCATGACACTTGGATATCTGGCACCTTACCCAAGGCTAGGAATAGGAACTACAATGTTAATTC T G AC022882.1 Ensembl:ENSG00000213604 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1338494521 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1869692,Human_miRNA_ID_1911428 44524 RMVar_ID_44524 Human_SNP_ID_467949081 A-to-I Human chr11 - 57494046 57494046 57494046 CCAGAAGGCCCCCAGCCTGGAGGACGGTTCGGATGCCTTCATGTCACCCCAGGATGTTCGGGGCA CCAGAAGGCCCCCAGCCTGGAGGACGGTTCGGGTGCCTTCATGTCACCCCAGGATGTTCGGGGCA T C SLC43A1 Ensembl:ENSG00000149150 Protein coding CDS GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs960901999 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1240013,Human_Splice_Rec_1240041,Human_Splice_Rec_1240065,Human_Splice_Rec_1240077,Human_Splice_Rec_1240093 Human_miRNA_ID_2932107 RMVar_hsa_circ_120358,RMVar_hsa_circ_70359,RMVar_hsa_circ_303725,RMVar_hsa_circ_373537,RMVar_hsa_circ_149767,RMVar_hsa_circ_149768,RMVar_hsa_circ_94502,RMVar_hsa_circ_103721,RMVar_hsa_circ_149771,RMVar_hsa_circ_149773,RMVar_hsa_circ_149772,RMVar_hsa_circ_77455,RMVar_hsa_circ_86727,RMVar_hsa_circ_52394,RMVar_hsa_circ_114013,RMVar_hsa_circ_149777,RMVar_hsa_circ_149778,RMVar_hsa_circ_149780,RMVar_hsa_circ_45251,RMVar_hsa_circ_55147,RMVar_hsa_circ_327059,RMVar_hsa_circ_149782 44525 RMVar_ID_44525 Human_SNP_ID_467949317 A-to-I Human chr11 - 57495051 57495051 57495051 CTGAGGTCGGGAGTTCTAGACCAGCCTGACCAACATGGAGAAACACCGTCTCTACTAAAAATACA CTGAGGTCGGGAGTTCTAGACCAGCCTGACCATCATGGAGAAACACCGTCTCTACTAAAAATACA T A SLC43A1 Ensembl:ENSG00000149150 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1404512708 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120358,RMVar_hsa_circ_70359,RMVar_hsa_circ_373537,RMVar_hsa_circ_149768,RMVar_hsa_circ_94502,RMVar_hsa_circ_103721,RMVar_hsa_circ_149771,RMVar_hsa_circ_149773,RMVar_hsa_circ_149772,RMVar_hsa_circ_77455,RMVar_hsa_circ_86727,RMVar_hsa_circ_114013,RMVar_hsa_circ_149777,RMVar_hsa_circ_149778,RMVar_hsa_circ_149780,RMVar_hsa_circ_45251,RMVar_hsa_circ_55147,RMVar_hsa_circ_327059,RMVar_hsa_circ_149782 44526 RMVar_ID_44526 Human_SNP_ID_467951584 A-to-I Human chr11 - 57503612 57503612 57503612 AATGCAGATAAACCTGTAGAGAGGCCGGGCACAGTTGCTCATGTCTGTAATCTCAGCACTTTGGG AATGCAGATAAACCTGTAGAGAGGCCGGGCACTGTTGCTCATGTCTGTAATCTCAGCACTTTGGG T A SLC43A1 Ensembl:ENSG00000149150 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1001733974 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70359,RMVar_hsa_circ_94502,RMVar_hsa_circ_149771,RMVar_hsa_circ_86727,RMVar_hsa_circ_31946,RMVar_hsa_circ_149778,RMVar_hsa_circ_45251 44527 RMVar_ID_44527 Human_SNP_ID_467951585 A-to-I Human chr11 - 57503612 57503612 57503612 AATGCAGATAAACCTGTAGAGAGGCCGGGCACAGTTGCTCATGTCTGTAATCTCAGCACTTTGGG AATGCAGATAAACCTGTAGAGAGGCCGGGCACGGTTGCTCATGTCTGTAATCTCAGCACTTTGGG T C SLC43A1 Ensembl:ENSG00000149150 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1001733974 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70359,RMVar_hsa_circ_94502,RMVar_hsa_circ_149771,RMVar_hsa_circ_86727,RMVar_hsa_circ_31946,RMVar_hsa_circ_149778,RMVar_hsa_circ_45251 44528 RMVar_ID_44528 Human_SNP_ID_467951586 A-to-I Human chr11 - 57503612 57503612 57503612 AATGCAGATAAACCTGTAGAGAGGCCGGGCACAGTTGCTCATGTCTGTAATCTCAGCACTTTGGG AATGCAGATAAACCTGTAGAGAGGCCGGGCACCGTTGCTCATGTCTGTAATCTCAGCACTTTGGG T G SLC43A1 Ensembl:ENSG00000149150 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1001733974 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70359,RMVar_hsa_circ_94502,RMVar_hsa_circ_149771,RMVar_hsa_circ_86727,RMVar_hsa_circ_31946,RMVar_hsa_circ_149778,RMVar_hsa_circ_45251 44529 RMVar_ID_44529 Human_SNP_ID_467959390 A-to-I Human chr11 - 57536710 57536710 57536710 AAATTGGCCGGGCTTGGTGGCGCATGCCTGTAATCTCAGCTACTTGGGAGGCTGAGGCACGAGAA AAATTGGCCGGGCTTGGTGGCGCATGCCTGTATTCTCAGCTACTTGGGAGGCTGAGGCACGAGAA T A lnc-TIMM10-1 RNACentral:URS00008BFDFD lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1178057229 Functional Loss SNV dbSNP153 33..33 33 - - - 44530 RMVar_ID_44530 Human_SNP_ID_467969717 A-to-I Human chr11 - 57576704 57576704 57576704 GAGGCCAAGTACAAGTGGTGCAAAGTGAGAAAAATCTTTGTGGACACCAAAGGAATCCCTCATCT GAGGCCAAGTACAAGTGGTGCAAAGTGAGAAAGATCTTTGTGGACACCAAAGGAATCCCTCATCT T C RPS4XP13 Ensembl:ENSG00000240371 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879098042 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1911429 44531 RMVar_ID_44531 Human_SNP_ID_467986091 A-to-I Human chr11 + 57642365 57642365 57642365 AAAATTAGCCAGGCGTGGTAATGCACGCCTGTAGTCTCAGCTACTTGGGTGGCTGAGGCAGGAGA AAAATTAGCCAGGCGTGGTAATGCACGCCTGTCGTCTCAGCTACTTGGGTGGCTGAGGCAGGAGA A C AP000662.1 Ensembl:ENSG00000254602 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1177337314 Functional Loss SNV dbSNP153 33..33 33 - - - 44532 RMVar_ID_44532 Human_SNP_ID_467986092 A-to-I Human chr11 + 57642365 57642365 57642365 AAAATTAGCCAGGCGTGGTAATGCACGCCTGTAGTCTCAGCTACTTGGGTGGCTGAGGCAGGAGA AAAATTAGCCAGGCGTGGTAATGCACGCCTGTTGTCTCAGCTACTTGGGTGGCTGAGGCAGGAGA A T AP000662.1 Ensembl:ENSG00000254602 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1177337314 Functional Loss SNV dbSNP153 33..33 33 - - - 44533 RMVar_ID_44533 Human_SNP_ID_467989139 A-to-I Human chr11 + 57653779 57653779 57653779 TTGTTTGTTTGTTTGTTTGTTCTTTGAAATGGAATCTCGCTCTGTTTCCCAGGCTGGAGTGCAAT TTGTTTGTTTGTTTGTTTGTTCTTTGAAATGGCATCTCGCTCTGTTTCCCAGGCTGGAGTGCAAT A C CLP1 Ensembl:ENSG00000172409 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs567764885 Functional Loss SNV dbSNP153 33..33 33 - - - 44534 RMVar_ID_44534 Human_SNP_ID_467993482 A-to-I Human chr11 + 57670301 57670301 57670301 CGAGACCAGCCTGGGCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAATTAGCTGGGTGT CGAGACCAGCCTGGGCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAATTAGCTGGGTGT A G ZDHHC5 Ensembl:ENSG00000156599 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1056656182 Functional Loss SNV dbSNP153 33..33 33 - - - 44535 RMVar_ID_44535 Human_SNP_ID_467993483 A-to-I Human chr11 + 57670301 57670301 57670301 CGAGACCAGCCTGGGCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAATTAGCTGGGTGT CGAGACCAGCCTGGGCAACATGGTGAAACCCCTTCTCTACTAAAAATACAAAATTAGCTGGGTGT A T ZDHHC5 Ensembl:ENSG00000156599 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1056656182 Functional Loss SNV dbSNP153 33..33 33 - - - 44536 RMVar_ID_44536 Human_SNP_ID_467993513 A-to-I Human chr11 + 57670391 57670391 57670391 TGCTCGGGAGGCTGAGACAGGAGAATTGCTTGAATCCGGGACTCGGAGGTTGCAGTGAGCTGAGA TGCTCGGGAGGCTGAGACAGGAGAATTGCTTGCATCCGGGACTCGGAGGTTGCAGTGAGCTGAGA A C ZDHHC5 Ensembl:ENSG00000156599 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215359076 Functional Loss SNV dbSNP153 33..33 33 - - - 44537 RMVar_ID_44537 Human_SNP_ID_467996775 A-to-I Human chr11 + 57684112 57684112 57684112 CTCCCACCTCAGCCTCCAGAATTGCTGGGACTACAGGCGCGGGCCACCACACACAGCTAATTTTT CTCCCACCTCAGCCTCCAGAATTGCTGGGACTGCAGGCGCGGGCCACCACACACAGCTAATTTTT A G ZDHHC5 Ensembl:ENSG00000156599 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1415808017 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2806,RMVar_hsa_circ_269514,RMVar_hsa_circ_73667,RMVar_hsa_circ_288914,RMVar_hsa_circ_312707,RMVar_hsa_circ_107222,RMVar_hsa_circ_149792,RMVar_hsa_circ_149793,RMVar_hsa_circ_149791 44538 RMVar_ID_44538 Human_SNP_ID_467996784 A-to-I Human chr11 + 57684134 57684134 57684134 TGCTGGGACTACAGGCGCGGGCCACCACACACAGCTAATTTTTCTATACCTATTCTTGGTAGAGA TGCTGGGACTACAGGCGCGGGCCACCACACACTGCTAATTTTTCTATACCTATTCTTGGTAGAGA A T ZDHHC5 Ensembl:ENSG00000156599 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1278939409 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2806,RMVar_hsa_circ_269514,RMVar_hsa_circ_73667,RMVar_hsa_circ_288914,RMVar_hsa_circ_312707,RMVar_hsa_circ_107222,RMVar_hsa_circ_149792,RMVar_hsa_circ_149793,RMVar_hsa_circ_149791 44539 RMVar_ID_44539 Human_SNP_ID_467996960 A-to-I Human chr11 + 57684891 57684890 57684891 CACTGTAGGCTTGGCGTGGTGGCTCACATCTTAATCCCAGCACTTTGGGAGGCCAAGGTGGGCAG CACTGTAGGCTTGGCGTGGTGGCTCACATCTT_ATCCCAGCACTTTGGGAGGCCAAGGTGGGCAG TA T ZDHHC5 Ensembl:ENSG00000156599 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs762038239 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_2806,RMVar_hsa_circ_269514,RMVar_hsa_circ_73667,RMVar_hsa_circ_288914,RMVar_hsa_circ_312707,RMVar_hsa_circ_107222,RMVar_hsa_circ_149792,RMVar_hsa_circ_149793,RMVar_hsa_circ_149791 44540 RMVar_ID_44540 Human_SNP_ID_467996962 A-to-I Human chr11 + 57684891 57684891 57684891 CACTGTAGGCTTGGCGTGGTGGCTCACATCTTAATCCCAGCACTTTGGGAGGCCAAGGTGGGCAG CACTGTAGGCTTGGCGTGGTGGCTCACATCTTTATCCCAGCACTTTGGGAGGCCAAGGTGGGCAG A T ZDHHC5 Ensembl:ENSG00000156599 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1380169779 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2806,RMVar_hsa_circ_269514,RMVar_hsa_circ_73667,RMVar_hsa_circ_288914,RMVar_hsa_circ_312707,RMVar_hsa_circ_107222,RMVar_hsa_circ_149792,RMVar_hsa_circ_149793,RMVar_hsa_circ_149791 44541 RMVar_ID_44541 Human_SNP_ID_467996994 A-to-I Human chr11 + 57685037 57685037 57685037 CGACATGGTGGTGGGTGCCTGTGATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAG CGACATGGTGGTGGGTGCCTGTGATCCCAGCTGCTTGGGAGGCTGAGGCAGGAGAATCGCTTGAG A G ZDHHC5 Ensembl:ENSG00000156599 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs933353872 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2806,RMVar_hsa_circ_269514,RMVar_hsa_circ_73667,RMVar_hsa_circ_288914,RMVar_hsa_circ_312707,RMVar_hsa_circ_107222,RMVar_hsa_circ_149792,RMVar_hsa_circ_149793,RMVar_hsa_circ_149791 44542 RMVar_ID_44542 Human_SNP_ID_467997106 A-to-I Human chr11 + 57685482 57685482 57685482 CAGCCTGGCCAACATGGCGAAACCCCGTCTCTACTAAAAATATAAAAATTAGCCAGGCATGGTAG CAGCCTGGCCAACATGGCGAAACCCCGTCTCTGCTAAAAATATAAAAATTAGCCAGGCATGGTAG A G ZDHHC5 Ensembl:ENSG00000156599 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs950234065 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2806,RMVar_hsa_circ_269514,RMVar_hsa_circ_73667,RMVar_hsa_circ_288914,RMVar_hsa_circ_312707,RMVar_hsa_circ_107222,RMVar_hsa_circ_149792,RMVar_hsa_circ_149793,RMVar_hsa_circ_149791 44543 RMVar_ID_44543 Human_SNP_ID_467997367 A-to-I Human chr11 + 57686525 57686525 57686525 TTTAGTAGAGATGGGGTCTCACCATGTTGGCCAAGCTACTCTGGAACTCCTGACCTCAAATGATC TTTAGTAGAGATGGGGTCTCACCATGTTGGCCGAGCTACTCTGGAACTCCTGACCTCAAATGATC A G ZDHHC5 Ensembl:ENSG00000156599 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404713677 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2806,RMVar_hsa_circ_269514,RMVar_hsa_circ_73667,RMVar_hsa_circ_288914,RMVar_hsa_circ_312707,RMVar_hsa_circ_107222,RMVar_hsa_circ_149792,RMVar_hsa_circ_149793,RMVar_hsa_circ_149791 44544 RMVar_ID_44544 Human_SNP_ID_467997496 A-to-I Human chr11 + 57687105 57687105 57687105 TGCCCTCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGTACCCAGCTGTACAGT TGCCCTCCTTGGCCTCCCAAAGTGCTGGGATTTCAGGCATGAGCCACCGTACCCAGCTGTACAGT A T ZDHHC5 Ensembl:ENSG00000156599 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1565194682 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2806,RMVar_hsa_circ_269514,RMVar_hsa_circ_73667,RMVar_hsa_circ_288914,RMVar_hsa_circ_312707,RMVar_hsa_circ_107222,RMVar_hsa_circ_149792,RMVar_hsa_circ_149793,RMVar_hsa_circ_149791 44545 RMVar_ID_44545 Human_SNP_ID_467997583 A-to-I Human chr11 + 57687450 57687450 57687450 AAAAATTAGCTGCCGAAGTGGCGTGCGCCTGTAATCCCAGCTGTTTGGGAGGCTGAGACAGAAGT AAAAATTAGCTGCCGAAGTGGCGTGCGCCTGTGATCCCAGCTGTTTGGGAGGCTGAGACAGAAGT A G ZDHHC5 Ensembl:ENSG00000156599 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1052294110 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2806,RMVar_hsa_circ_269514,RMVar_hsa_circ_73667,RMVar_hsa_circ_288914,RMVar_hsa_circ_312707,RMVar_hsa_circ_107222,RMVar_hsa_circ_149792,RMVar_hsa_circ_149793,RMVar_hsa_circ_149791 44546 RMVar_ID_44546 Human_SNP_ID_468007175 A-to-I Human chr11 + 57719724 57719724 57719724 TTTTTTGTAGAGATGGGGTTTCGCCATGTTGCACAGGCTGATCTTGAACTCCTGGGCTCAAGTGG TTTTTTGTAGAGATGGGGTTTCGCCATGTTGCGCAGGCTGATCTTGAACTCCTGGGCTCAAGTGG A G AP001931.2,TMX2 Ensembl:ENSG00000288534,Ensembl:ENSG00000213593 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928072290 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123482,RMVar_hsa_circ_149806,RMVar_hsa_circ_83957,RMVar_hsa_circ_149805 44547 RMVar_ID_44547 Human_SNP_ID_468007191 A-to-I Human chr11 + 57719792 57719792 57719792 ATTTTCCCTCAGCCTCCCAAAGTGCTGGGACTATAGGCATGAACTACTGCACCCTGCCTTGAAAA ATTTTCCCTCAGCCTCCCAAAGTGCTGGGACTGTAGGCATGAACTACTGCACCCTGCCTTGAAAA A G AP001931.2,TMX2 Ensembl:ENSG00000288534,Ensembl:ENSG00000213593 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1460629177 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11643523,Human_RBP_ID_17559965 RMVar_hsa_circ_123482,RMVar_hsa_circ_149806,RMVar_hsa_circ_83957,RMVar_hsa_circ_149805 44548 RMVar_ID_44548 Human_SNP_ID_468007426 A-to-I Human chr11 + 57720603 57720599 57720603 TTGTATTTTAGTGGAGACAGTTTCACCACGTTAGTTAGGCTGATCTCGAACTTCTGGCCTCAAGC TTGTATTTTAGTGGAGACAGTTTCACCAC____GTTAGGCTGATCTCGAACTTCTGGCCTCAAGC CGTTA C AP001931.2,TMX2 Ensembl:ENSG00000288534,Ensembl:ENSG00000213593 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1177811797 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_11643536 RMVar_hsa_circ_123482,RMVar_hsa_circ_149806,RMVar_hsa_circ_83957,RMVar_hsa_circ_149805 44549 RMVar_ID_44549 Human_SNP_ID_468013131 A-to-I Human chr11 + 57740885 57740885 57740885 ACTTTCCTTTGTGTGGTAGGACTTGGAGGAGAAATCCCCTGGACTTTCACTAACCCTCTGACATA ACTTTCCTTTGTGTGGTAGGACTTGGAGGAGAGATCCCCTGGACTTTCACTAACCCTCTGACATA A G AP001931.2,TMX2 Ensembl:ENSG00000288534,Ensembl:ENSG00000213593 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1466782434 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_397720,Human_RBP_ID_8352932,Human_RBP_ID_26408464,Human_RBP_ID_26803470,Human_RBP_ID_27412282 Human_miRNA_ID_2378139,Human_miRNA_ID_3093212 RMVar_hsa_circ_95247,RMVar_hsa_circ_123482,RMVar_hsa_circ_149806,RMVar_hsa_circ_83957,RMVar_hsa_circ_149805,RMVar_hsa_circ_149808,RMVar_hsa_circ_116598,RMVar_hsa_circ_149810,RMVar_hsa_circ_125252,RMVar_hsa_circ_149811 44550 RMVar_ID_44550 Human_SNP_ID_468013140 A-to-I Human chr11 + 57740917 57740917 57740917 AATCCCCTGGACTTTCACTAACCCTCTGACATACTCCCCACACCCAGTTGATGGCTTTCCGTAAT AATCCCCTGGACTTTCACTAACCCTCTGACATCCTCCCCACACCCAGTTGATGGCTTTCCGTAAT A C AP001931.2,TMX2 Ensembl:ENSG00000288534,Ensembl:ENSG00000213593 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910292698 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_32003,Human_RBP_ID_397720,Human_RBP_ID_8352932,Human_RBP_ID_11643940,Human_RBP_ID_17232315,Human_RBP_ID_17348702,Human_RBP_ID_17465034,Human_RBP_ID_23508947,Human_RBP_ID_24403300,Human_RBP_ID_26408464,Human_RBP_ID_26803470,Human_RBP_ID_27202375,Human_RBP_ID_27412282,Human_RBP_ID_27556846 Human_miRNA_ID_1450762,Human_miRNA_ID_2367226,Human_miRNA_ID_2725784,Human_miRNA_ID_3015024 RMVar_hsa_circ_95247,RMVar_hsa_circ_123482,RMVar_hsa_circ_149806,RMVar_hsa_circ_83957,RMVar_hsa_circ_149805,RMVar_hsa_circ_149808,RMVar_hsa_circ_116598,RMVar_hsa_circ_149810,RMVar_hsa_circ_125252,RMVar_hsa_circ_149811 44551 RMVar_ID_44551 Human_SNP_ID_468020174 A-to-I Human chr11 + 57767111 57767111 57767111 CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGTGCGCGCCACCACGCCCTGCTAATTTTT CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTGCAGGTGCGCGCCACCACGCCCTGCTAATTTTT A G AP001931.2,CTNND1,AP001931.1 Ensembl:ENSG00000288534,Ensembl:ENSG00000198561,Ensembl:ENSG00000254732 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs950869266 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_149806,RMVar_hsa_circ_83957,RMVar_hsa_circ_149812 44552 RMVar_ID_44552 Human_SNP_ID_468020175 A-to-I Human chr11 + 57767113 57767113 57767113 CCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGTGCGCGCCACCACGCCCTGCTAATTTTTTG CCTGCCTCAGCCTCCCAAGTAGCTGGGACTACCGGTGCGCGCCACCACGCCCTGCTAATTTTTTG A C AP001931.2,CTNND1,AP001931.1 Ensembl:ENSG00000288534,Ensembl:ENSG00000198561,Ensembl:ENSG00000254732 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1457553647 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_149806,RMVar_hsa_circ_83957,RMVar_hsa_circ_149812 44553 RMVar_ID_44553 Human_SNP_ID_468020800 A-to-I Human chr11 + 57769424 57769424 57769424 CTCCTACTTCAGCCCCTGGAGTAGCTGGGACTACAGGCACACACCACCTTGCCTGGCTATTTAAG CTCCTACTTCAGCCCCTGGAGTAGCTGGGACTGCAGGCACACACCACCTTGCCTGGCTATTTAAG A G AP001931.2,CTNND1,AP001931.1 Ensembl:ENSG00000288534,Ensembl:ENSG00000198561,Ensembl:ENSG00000254732 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs975357136 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17559973 RMVar_hsa_circ_149806,RMVar_hsa_circ_83957,RMVar_hsa_circ_149812 44554 RMVar_ID_44554 Human_SNP_ID_468023874 A-to-I Human chr11 + 57783396 57783396 57783396 CACTGATAAGAAGCCATAGAAAGGCCGGGCTCACGCCTGTAATCCCAGCACTTTGGAAGGCCGCG CACTGATAAGAAGCCATAGAAAGGCCGGGCTCCCGCCTGTAATCCCAGCACTTTGGAAGGCCGCG A C AP001931.2,CTNND1,AP001931.1 Ensembl:ENSG00000288534,Ensembl:ENSG00000198561,Ensembl:ENSG00000254732 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1387988720 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_149806,RMVar_hsa_circ_83957,RMVar_hsa_circ_149812 44555 RMVar_ID_44555 Human_SNP_ID_468023926 A-to-I Human chr11 + 57783544 57783544 57783544 AGCCGGGCGTGTTGGCGGGCGCCTGTGGTCCCAGCTACTGGGGAGGCTGAGGCAGGAGAATGCTG AGCCGGGCGTGTTGGCGGGCGCCTGTGGTCCCCGCTACTGGGGAGGCTGAGGCAGGAGAATGCTG A C AP001931.2,CTNND1,AP001931.1 Ensembl:ENSG00000288534,Ensembl:ENSG00000198561,Ensembl:ENSG00000254732 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1411913115 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_149806,RMVar_hsa_circ_83957,RMVar_hsa_circ_149812 44556 RMVar_ID_44556 Human_SNP_ID_468023928 A-to-I Human chr11 + 57783548 57783548 57783548 GGGCGTGTTGGCGGGCGCCTGTGGTCCCAGCTACTGGGGAGGCTGAGGCAGGAGAATGCTGTGAA GGGCGTGTTGGCGGGCGCCTGTGGTCCCAGCTGCTGGGGAGGCTGAGGCAGGAGAATGCTGTGAA A G AP001931.2,CTNND1,AP001931.1 Ensembl:ENSG00000288534,Ensembl:ENSG00000198561,Ensembl:ENSG00000254732 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs899380727 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_149806,RMVar_hsa_circ_83957,RMVar_hsa_circ_149812 44557 RMVar_ID_44557 Human_SNP_ID_468024205 A-to-I Human chr11 + 57784706 57784706 57784706 TTTTGTATTTTAAGTAGAGATGGGGTTTCACCATGTTGACCAGGCTGGTTTCGAACTCCTGAACT TTTTGTATTTTAAGTAGAGATGGGGTTTCACCGTGTTGACCAGGCTGGTTTCGAACTCCTGAACT A G AP001931.2,CTNND1,AP001931.1 Ensembl:ENSG00000288534,Ensembl:ENSG00000198561,Ensembl:ENSG00000254732 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1008543759 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_149806,RMVar_hsa_circ_83957,RMVar_hsa_circ_149812 44558 RMVar_ID_44558 Human_SNP_ID_468027363 A-to-I Human chr11 + 57797360 57797360 57797360 TCAAGTGATTCTCATGCCTCAGCCTCCCTAGTAGTTGGGACTACAGGCAAGCACCATCACGCCTG TCAAGTGATTCTCATGCCTCAGCCTCCCTAGTGGTTGGGACTACAGGCAAGCACCATCACGCCTG A G AP001931.2,CTNND1,AP001931.1 Ensembl:ENSG00000288534,Ensembl:ENSG00000198561,Ensembl:ENSG00000254732 Protein coding,Protein coding,Protein coding intron,intron,intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs987911965 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3136,RMVar_hsa_circ_329850,RMVar_hsa_circ_101129,RMVar_hsa_circ_91947,RMVar_hsa_circ_149813,RMVar_hsa_circ_149817,RMVar_hsa_circ_279803,RMVar_hsa_circ_63458,RMVar_hsa_circ_121759,RMVar_hsa_circ_349348,RMVar_hsa_circ_360399,RMVar_hsa_circ_376434,RMVar_hsa_circ_327733,RMVar_hsa_circ_287006,RMVar_hsa_circ_37665,RMVar_hsa_circ_40750,RMVar_hsa_circ_149819,RMVar_hsa_circ_149820,RMVar_hsa_circ_149822,RMVar_hsa_circ_291974,RMVar_hsa_circ_328842,RMVar_hsa_circ_358006,RMVar_hsa_circ_55428 44559 RMVar_ID_44559 Human_SNP_ID_468027495 A-to-I Human chr11 + 57797791 57797791 57797791 ATGAACCCGGGAGGCAGAGGTTGTGGTGAGCCAAGATCATGCCATTGCACTCCAGCCTGGGCAAC ATGAACCCGGGAGGCAGAGGTTGTGGTGAGCCGAGATCATGCCATTGCACTCCAGCCTGGGCAAC A G AP001931.2,CTNND1,AP001931.1 Ensembl:ENSG00000288534,Ensembl:ENSG00000198561,Ensembl:ENSG00000254732 Protein coding,Protein coding,Protein coding intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1248764657 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3136,RMVar_hsa_circ_329850,RMVar_hsa_circ_101129,RMVar_hsa_circ_91947,RMVar_hsa_circ_149813,RMVar_hsa_circ_149817,RMVar_hsa_circ_279803,RMVar_hsa_circ_63458,RMVar_hsa_circ_121759,RMVar_hsa_circ_349348,RMVar_hsa_circ_360399,RMVar_hsa_circ_376434,RMVar_hsa_circ_327733,RMVar_hsa_circ_287006,RMVar_hsa_circ_37665,RMVar_hsa_circ_40750,RMVar_hsa_circ_149819,RMVar_hsa_circ_149820,RMVar_hsa_circ_149822,RMVar_hsa_circ_291974,RMVar_hsa_circ_328842,RMVar_hsa_circ_358006,RMVar_hsa_circ_55428 44560 RMVar_ID_44560 Human_SNP_ID_468027721 A-to-I Human chr11 + 57798511 57798511 57798511 AAACTTTGACCTCACAAGGGCCTTGACATTCTATGCTTAGGGTCTTATTATTTGATTGTAAAGTG AAACTTTGACCTCACAAGGGCCTTGACATTCTGTGCTTAGGGTCTTATTATTTGATTGTAAAGTG A G AP001931.2,CTNND1,AP001931.1 Ensembl:ENSG00000288534,Ensembl:ENSG00000198561,Ensembl:ENSG00000254732 Protein coding,Protein coding,Protein coding intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10736687 Functional Loss SNV dbSNP153,EGP 33..33 33 - - - RMVar_hsa_circ_3136,RMVar_hsa_circ_329850,RMVar_hsa_circ_101129,RMVar_hsa_circ_91947,RMVar_hsa_circ_149813,RMVar_hsa_circ_149817,RMVar_hsa_circ_279803,RMVar_hsa_circ_63458,RMVar_hsa_circ_121759,RMVar_hsa_circ_349348,RMVar_hsa_circ_360399,RMVar_hsa_circ_376434,RMVar_hsa_circ_327733,RMVar_hsa_circ_287006,RMVar_hsa_circ_37665,RMVar_hsa_circ_40750,RMVar_hsa_circ_149819,RMVar_hsa_circ_149820,RMVar_hsa_circ_149822,RMVar_hsa_circ_291974,RMVar_hsa_circ_328842,RMVar_hsa_circ_358006,RMVar_hsa_circ_55428 44561 RMVar_ID_44561 Human_SNP_ID_468028190 A-to-I Human chr11 + 57800468 57800468 57800468 TTTTGTATTTTTAGTAGAGATGGTGTTTTTCCATGTTGGCCATGCTGGTCTCGAACTTCTGACCT TTTTGTATTTTTAGTAGAGATGGTGTTTTTCCGTGTTGGCCATGCTGGTCTCGAACTTCTGACCT A G AP001931.2,CTNND1,AP001931.1 Ensembl:ENSG00000288534,Ensembl:ENSG00000198561,Ensembl:ENSG00000254732 Protein coding,Protein coding,Protein coding intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1472391916 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11645580 RMVar_hsa_circ_3136,RMVar_hsa_circ_329850,RMVar_hsa_circ_101129,RMVar_hsa_circ_91947,RMVar_hsa_circ_149813,RMVar_hsa_circ_149817,RMVar_hsa_circ_279803,RMVar_hsa_circ_63458,RMVar_hsa_circ_121759,RMVar_hsa_circ_349348,RMVar_hsa_circ_360399,RMVar_hsa_circ_376434,RMVar_hsa_circ_327733,RMVar_hsa_circ_287006,RMVar_hsa_circ_37665,RMVar_hsa_circ_40750,RMVar_hsa_circ_149819,RMVar_hsa_circ_149820,RMVar_hsa_circ_149822,RMVar_hsa_circ_291974,RMVar_hsa_circ_328842,RMVar_hsa_circ_358006,RMVar_hsa_circ_55428 44562 RMVar_ID_44562 Human_SNP_ID_468028199 A-to-I Human chr11 + 57800520 57800520 57800520 GAACTTCTGACCTCAGGTAATCCGCCCACTGCAGCCTCCCAAAGTGCTGGGATTACAGATGTGAG GAACTTCTGACCTCAGGTAATCCGCCCACTGCGGCCTCCCAAAGTGCTGGGATTACAGATGTGAG A G AP001931.2,CTNND1,AP001931.1 Ensembl:ENSG00000288534,Ensembl:ENSG00000198561,Ensembl:ENSG00000254732 Protein coding,Protein coding,Protein coding intron,intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1024787622 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11760019 RMVar_hsa_circ_3136,RMVar_hsa_circ_329850,RMVar_hsa_circ_101129,RMVar_hsa_circ_91947,RMVar_hsa_circ_149813,RMVar_hsa_circ_149817,RMVar_hsa_circ_279803,RMVar_hsa_circ_63458,RMVar_hsa_circ_121759,RMVar_hsa_circ_349348,RMVar_hsa_circ_360399,RMVar_hsa_circ_376434,RMVar_hsa_circ_327733,RMVar_hsa_circ_287006,RMVar_hsa_circ_37665,RMVar_hsa_circ_40750,RMVar_hsa_circ_149819,RMVar_hsa_circ_149820,RMVar_hsa_circ_149822,RMVar_hsa_circ_291974,RMVar_hsa_circ_328842,RMVar_hsa_circ_358006,RMVar_hsa_circ_55428 44563 RMVar_ID_44563 Human_SNP_ID_468035819 A-to-I Human chr11 + 57834320 57834320 57834320 AAAATTAGCCGGGTGTGGGATCACGTGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGGAGAAGG AAAATTAGCCGGGTGTGGGATCACGTGCCTGTGGTCCCAGCTACTCAGGAGGCTGAGGGAGAAGG A G HSALNG0084319 RNACentral:URS0000EA7C67 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1219895200 Functional Loss SNV dbSNP153 33..33 33 - - - 44564 RMVar_ID_44564 Human_SNP_ID_468035821 A-to-I Human chr11 + 57834334 57834334 57834334 GTGGGATCACGTGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGGAGAAGGATCATTTGAACATG GTGGGATCACGTGCCTGTAGTCCCAGCTACTCTGGAGGCTGAGGGAGAAGGATCATTTGAACATG A T HSALNG0084319 RNACentral:URS0000EA7C67 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs769742457 Functional Loss SNV dbSNP153 33..33 33 - - - 44565 RMVar_ID_44565 Human_SNP_ID_468081122 A-to-I Human chr11 + 58025459 58025459 58025459 CTTGACCTTGTGATCCGCCCGCTCAGCCTCCCAAGGTGTTGGGATTGCAGGCGTGAGCCACTGCG CTTGACCTTGTGATCCGCCCGCTCAGCCTCCCGAGGTGTTGGGATTGCAGGCGTGAGCCACTGCG A G OR9Q1 Ensembl:ENSG00000186509 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs912020245 Functional Loss SNV dbSNP153 33..33 33 - - - 44566 RMVar_ID_44566 Human_SNP_ID_468210192 A-to-I Human chr11 - 58540868 58540868 58540868 ATAGTTGAAAAGTATTTATTTTGCGGCTATTCATTGATTTGTGAGGTGCACTTGTTTTAAAAGGT ATAGTTGAAAAGTATTTATTTTGCGGCTATTCGTTGATTTGTGAGGTGCACTTGTTTTAAAAGGT T C LPXN Ensembl:ENSG00000110031 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2510549 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5036,GWAS_ID_5037,GWAS_ID_5038,GWAS_ID_5039,GWAS_ID_5040,GWAS_ID_5041,GWAS_ID_5042,GWAS_ID_5043,GWAS_ID_5044,GWAS_ID_5045,GWAS_ID_5046,GWAS_ID_5047,GWAS_ID_5048,GWAS_ID_5049,GWAS_ID_5050,GWAS_ID_5051,GWAS_ID_5052,GWAS_ID_5053,GWAS_ID_5054,GWAS_ID_5055,GWAS_ID_5056,GWAS_ID_5057,GWAS_ID_5058,GWAS_ID_5059,GWAS_ID_5060,GWAS_ID_5061,GWAS_ID_5062,GWAS_ID_5063,GWAS_ID_5064,GWAS_ID_5065,GWAS_ID_5066,GWAS_ID_5067,GWAS_ID_5068 44567 RMVar_ID_44567 Human_SNP_ID_468361057 A-to-I Human chr11 - 59130416 59130416 59130416 GTAAAAGTCTGGAAAATTTGCAGCCTGACCATATGGTAGAAAAGAAAAACCCATTTTCTGGGAAG GTAAAAGTCTGGAAAATTTGCAGCCTGACCATGTGGTAGAAAAGAAAAACCCATTTTCTGGGAAG T C FAM111A-DT Ensembl:ENSG00000245571 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs375193032 Functional Loss SNV dbSNP153 33..33 33 - - - 44568 RMVar_ID_44568 Human_SNP_ID_468361125 A-to-I Human chr11 - 59130670 59130670 59130670 AAGAGGGAGCATGTGTAGGGGAACTCTCCTATATAACTATCAGATCTTGTGAGACTTATTCACTA AAGAGGGAGCATGTGTAGGGGAACTCTCCTATGTAACTATCAGATCTTGTGAGACTTATTCACTA T C FAM111A-DT Ensembl:ENSG00000245571 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1438303011 Functional Loss SNV dbSNP153 33..33 33 - - - 44569 RMVar_ID_44569 Human_SNP_ID_468361193 A-to-I Human chr11 - 59130954 59130954 59130954 CTGTCTTCTTCTGAGCCCCCTAACCTTTTCCAACCTCTGCCTGTTACCCAGTTCCAAAGTTGCTT CTGTCTTCTTCTGAGCCCCCTAACCTTTTCCAGCCTCTGCCTGTTACCCAGTTCCAAAGTTGCTT T C FAM111A-DT Ensembl:ENSG00000245571 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1012663313 Functional Loss SNV dbSNP153 33..33 33 - - - 44570 RMVar_ID_44570 Human_SNP_ID_468361194 A-to-I Human chr11 - 59130954 59130954 59130954 CTGTCTTCTTCTGAGCCCCCTAACCTTTTCCAACCTCTGCCTGTTACCCAGTTCCAAAGTTGCTT CTGTCTTCTTCTGAGCCCCCTAACCTTTTCCACCCTCTGCCTGTTACCCAGTTCCAAAGTTGCTT T G FAM111A-DT Ensembl:ENSG00000245571 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1012663313 Functional Loss SNV dbSNP153 33..33 33 - - - 44571 RMVar_ID_44571 Human_SNP_ID_468361205 A-to-I Human chr11 - 59131021 59131021 59131021 CACTATCACATTTTGGGCAAAGGCATTCGACAAGTCTCTATGAAGTTCCAAACTTTCCCACATTT CACTATCACATTTTGGGCAAAGGCATTCGACAGGTCTCTATGAAGTTCCAAACTTTCCCACATTT T C FAM111A-DT Ensembl:ENSG00000245571 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971176131 Functional Loss SNV dbSNP153 33..33 33 - - - 44572 RMVar_ID_44572 Human_SNP_ID_468361282 A-to-I Human chr11 - 59131386 59131386 59131386 ATTTACCCTCAGAAAATGAGGTTTTATCTTCTATCACATCGACGGGCTGCAAATTTTCTGAACTT ATTTACCCTCAGAAAATGAGGTTTTATCTTCTGTCACATCGACGGGCTGCAAATTTTCTGAACTT T C FAM111A-DT Ensembl:ENSG00000245571 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs571884956 Functional Loss SNV dbSNP153 33..33 33 - - - 44573 RMVar_ID_44573 Human_SNP_ID_468364906 A-to-I Human chr11 + 59146712 59146712 59146712 GTGGAATGGTTACGAGAGTAAACATAGCCTTTAGATAACTTCCATTTGACAAGAAATACAGGGGC GTGGAATGGTTACGAGAGTAAACATAGCCTTTGGATAACTTCCATTTGACAAGAAATACAGGGGC A G FAM111A Ensembl:ENSG00000166801 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,31158229,31158229,31158229 RNA-Seq:(High) rs1422095386 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102994,RMVar_hsa_circ_93537,RMVar_hsa_circ_149845,RMVar_hsa_circ_149846 44574 RMVar_ID_44574 Human_SNP_ID_468471655 A-to-I Human chr11 + 59554110 59554110 59554110 AGGAGGCCGAGGAAGGAGAATAGCTTGACCTCAGGAGGCGGAGGTTGCAGTGAGCTGAGATTGCG AGGAGGCCGAGGAAGGAGAATAGCTTGACCTCGGGAGGCGGAGGTTGCAGTGAGCTGAGATTGCG A G AP003778.1 Ensembl:ENSG00000287264 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1184060994 Functional Loss SNV dbSNP153 33..33 33 - - - 44575 RMVar_ID_44575 Human_SNP_ID_468478104 A-to-I Human chr11 - 59576041 59576041 59576041 CATCAAGTGTGTTCACACGCGGGGTCGGTTTAATGGAGTGTCCACGCGGAGATAACTGCGATATT CATCAAGTGTGTTCACACGCGGGGTCGGTTTAGTGGAGTGTCCACGCGGAGATAACTGCGATATT T C OSBP Ensembl:ENSG00000110048 Protein coding 3'UTR GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1375860817 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8353159,Human_RBP_ID_9004419,Human_RBP_ID_17804565,Human_RBP_ID_19647473 Human_miRNA_ID_264252 44576 RMVar_ID_44576 Human_SNP_ID_468481600 A-to-I Human chr11 - 59589554 59589554 59589554 CTGTGTTGCCCAGGCTGGAGGGCAGTGGTGCAATCTCTGCTTATTGCAACCTCCGCCTCCCAGGC CTGTGTTGCCCAGGCTGGAGGGCAGTGGTGCAGTCTCTGCTTATTGCAACCTCCGCCTCCCAGGC T C OSBP Ensembl:ENSG00000110048 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1010527733 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11648282,Human_RBP_ID_23267068 RMVar_hsa_circ_62772,RMVar_hsa_circ_149853,RMVar_hsa_circ_353202,RMVar_hsa_circ_371383 44577 RMVar_ID_44577 Human_SNP_ID_468482379 A-to-I Human chr11 - 59593002 59593002 59593002 TCTGAGCTCTGGAGTTCAAGACCAGCCTGGGCAACATGGTGAAACCCTGTCTTTACTAAGAATAC TCTGAGCTCTGGAGTTCAAGACCAGCCTGGGCGACATGGTGAAACCCTGTCTTTACTAAGAATAC T C OSBP Ensembl:ENSG00000110048 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1244552716 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_62772,RMVar_hsa_circ_149853,RMVar_hsa_circ_353202,RMVar_hsa_circ_371383 44578 RMVar_ID_44578 Human_SNP_ID_468482383 A-to-I Human chr11 - 59593016 59593016 59593016 GGGCAGGCAGATTGTCTGAGCTCTGGAGTTCAAGACCAGCCTGGGCAACATGGTGAAACCCTGTC GGGCAGGCAGATTGTCTGAGCTCTGGAGTTCAGGACCAGCCTGGGCAACATGGTGAAACCCTGTC T C OSBP Ensembl:ENSG00000110048 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1018754948 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_62772,RMVar_hsa_circ_149853,RMVar_hsa_circ_353202,RMVar_hsa_circ_371383 44579 RMVar_ID_44579 Human_SNP_ID_468482989 A-to-I Human chr11 - 59595718 59595718 59595718 CCAGGCTGGTCTCAAACTGCTGAGCACAAGCAATCCGCTTGCCTCAGCCTCTCAAAGTGCTAGGA CCAGGCTGGTCTCAAACTGCTGAGCACAAGCAGTCCGCTTGCCTCAGCCTCTCAAAGTGCTAGGA T C OSBP Ensembl:ENSG00000110048 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs978667810 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_53365,RMVar_hsa_circ_62772,RMVar_hsa_circ_353202,RMVar_hsa_circ_65801,RMVar_hsa_circ_352228 44580 RMVar_ID_44580 Human_SNP_ID_468482992 A-to-I Human chr11 - 59595736 59595736 59595736 GGTGTTTTGCCATGTTTCCCAGGCTGGTCTCAAACTGCTGAGCACAAGCAATCCGCTTGCCTCAG GGTGTTTTGCCATGTTTCCCAGGCTGGTCTCATACTGCTGAGCACAAGCAATCCGCTTGCCTCAG T A OSBP Ensembl:ENSG00000110048 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1282483053 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_53365,RMVar_hsa_circ_62772,RMVar_hsa_circ_353202,RMVar_hsa_circ_65801,RMVar_hsa_circ_352228 44581 RMVar_ID_44581 Human_SNP_ID_468521517 A-to-I Human chr11 - 59753839 59753839 59753839 CCGGCTAATTTTTGTGTTTTTTTCGTAGAGATAGGGTTTCGCCATGTTGCCCAGGCTGGTCTGGA CCGGCTAATTTTTGTGTTTTTTTCGTAGAGATGGGGTTTCGCCATGTTGCCCAGGCTGGTCTGGA T C AP000640.1 Ensembl:ENSG00000254477 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs561443928 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1242878 44582 RMVar_ID_44582 Human_SNP_ID_78150077 A-to-I Human chr2 + 75532013 75532013 75532013 AACCCCGTCTCTACTAAAAATACAAAAAAATTAGCCGGGTGTGGTGGCGGGTGCCTGTGGTCCCA AACCCCGTCTCTACTAAAAATACAAAAAAATTTGCCGGGTGTGGTGGCGGGTGCCTGTGGTCCCA A T AC007099.1 Ensembl:ENSG00000231172 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1221882533 Functional Loss SNV dbSNP153 33..33 33 - - - 44583 RMVar_ID_44583 Human_SNP_ID_78180266 A-to-I Human chr2 + 75656856 75656856 75656856 TGATGATTTATTCTCTGCTGCTTTGTTCTCCCAACTATTATTTGGATGTTGGATATCCAGCACTG TGATGATTTATTCTCTGCTGCTTTGTTCTCCCGACTATTATTTGGATGTTGGATATCCAGCACTG A G MRPL19 Ensembl:ENSG00000115364 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1212156041 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3634864,Human_RBP_ID_17508805,Human_RBP_ID_18766136,Human_RBP_ID_20604786,Human_RBP_ID_23886128,Human_RBP_ID_27698632 RMVar_hsa_circ_90220,RMVar_hsa_circ_201409 44584 RMVar_ID_44584 Human_SNP_ID_78181848 A-to-I Human chr2 + 75663649 75663648 75663650 GGGAGGTCAAGGTGGGTAGACTGCTTGAGCTCAAGAGTTCGAGACCAGCCTGGGCAATGTCACGA GGGAGGTCAAGGTGGGTAGACTGCTTGAGCTC__GAGTTCGAGACCAGCCTGGGCAATGTCACGA CAA C MRPL19 Ensembl:ENSG00000115364 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1316289507 Functional Loss DEL dbSNP153 33..34 33 - - - 44585 RMVar_ID_44585 Human_SNP_ID_78181849 A-to-I Human chr2 + 75663649 75663649 75663649 GGGAGGTCAAGGTGGGTAGACTGCTTGAGCTCAAGAGTTCGAGACCAGCCTGGGCAATGTCACGA GGGAGGTCAAGGTGGGTAGACTGCTTGAGCTCGAGAGTTCGAGACCAGCCTGGGCAATGTCACGA A G MRPL19 Ensembl:ENSG00000115364 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs988540605 Functional Loss SNV dbSNP153 33..33 33 - - - 44586 RMVar_ID_44586 Human_SNP_ID_78181855 A-to-I Human chr2 + 75663688 75663688 75663688 CGAGACCAGCCTGGGCAATGTCACGAAACCCCATCTCTACAAAAAATTACAAAAATCAGCTGGGC CGAGACCAGCCTGGGCAATGTCACGAAACCCCGTCTCTACAAAAAATTACAAAAATCAGCTGGGC A G MRPL19 Ensembl:ENSG00000115364 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992197318 Functional Loss SNV dbSNP153 33..33 33 - - - 44587 RMVar_ID_44587 Human_SNP_ID_78181870 A-to-I Human chr2 + 75663739 75663739 75663739 AAAATCAGCTGGGCATGGTGGCGCATGCCTATAGTCCCAGCTACTTGGGAGGTTGAAGTGGGAGG AAAATCAGCTGGGCATGGTGGCGCATGCCTATGGTCCCAGCTACTTGGGAGGTTGAAGTGGGAGG A G MRPL19 Ensembl:ENSG00000115364 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935902229 Functional Loss SNV dbSNP153 33..33 33 - - - 44588 RMVar_ID_44588 Human_SNP_ID_78182703 A-to-I Human chr2 - 75667171 75667171 75667171 AAAAACTGGAGAAACTGGTGCCTGAGTACAAAACTGGAATGCAAAAACCAACCCATTAAGAACCT AAAAACTGGAGAAACTGGTGCCTGAGTACAAAGCTGGAATGCAAAAACCAACCCATTAAGAACCT T C GCFC2 Ensembl:ENSG00000005436 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1176088110 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123888,RMVar_hsa_circ_74280,RMVar_hsa_circ_201410,RMVar_hsa_circ_288381,RMVar_hsa_circ_351461,RMVar_hsa_circ_201412 44589 RMVar_ID_44589 Human_SNP_ID_78182902 A-to-I Human chr2 + 75667980 75667980 75667980 TATATAGTTTTATGGCAGACTAGGTTTCCATTAGCAACCAGATGAATCAATTTCCACTAACCCTT TATATAGTTTTATGGCAGACTAGGTTTCCATTGGCAACCAGATGAATCAATTTCCACTAACCCTT A G MRPL19 Ensembl:ENSG00000115364 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs928315610 Functional Loss SNV dbSNP153 33..33 33 - - - 44590 RMVar_ID_44590 Human_SNP_ID_78182909 A-to-I Human chr2 + 75667996 75667996 75667996 AGACTAGGTTTCCATTAGCAACCAGATGAATCAATTTCCACTAACCCTTTTCTATAATTTTGATG AGACTAGGTTTCCATTAGCAACCAGATGAATCTATTTCCACTAACCCTTTTCTATAATTTTGATG A T MRPL19 Ensembl:ENSG00000115364 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs777369709 Functional Loss SNV dbSNP153 33..33 33 - - - 44591 RMVar_ID_44591 Human_SNP_ID_78182912 A-to-I Human chr2 + 75668019 75668019 75668019 AGATGAATCAATTTCCACTAACCCTTTTCTATAATTTTGATGAATGTGTAAGTTAAACATTAAAG AGATGAATCAATTTCCACTAACCCTTTTCTATGATTTTGATGAATGTGTAAGTTAAACATTAAAG A G MRPL19 Ensembl:ENSG00000115364 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs916109665 Functional Loss SNV dbSNP153 33..33 33 - - - 44592 RMVar_ID_44592 Human_SNP_ID_78182924 A-to-I Human chr2 + 75668048 75668048 75668048 TATAATTTTGATGAATGTGTAAGTTAAACATTAAAGAGCTAGAGAAACTGGTGCCTGAGTACAAG TATAATTTTGATGAATGTGTAAGTTAAACATTCAAGAGCTAGAGAAACTGGTGCCTGAGTACAAG A C MRPL19 Ensembl:ENSG00000115364 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1261810736 Functional Loss SNV dbSNP153 33..33 33 - - - 44593 RMVar_ID_44593 Human_SNP_ID_78182966 A-to-I Human chr2 + 75668225 75668225 75668225 TTAAGATTAAAAAACTTTCCAAGACTTTAGAGAAAGCTTTACAGACCCCAGACGGTAGTTAGATT TTAAGATTAAAAAACTTTCCAAGACTTTAGAGCAAGCTTTACAGACCCCAGACGGTAGTTAGATT A C MRPL19 Ensembl:ENSG00000115364 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs961890342 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22478311 44594 RMVar_ID_44594 Human_SNP_ID_78182990 A-to-I Human chr2 + 75668318 75668318 75668318 GTAGATGCACTCTCCCATGTAGCATGGAGCTTAGAATGCATATAAGTGCTAAAGAAAACAAAACA GTAGATGCACTCTCCCATGTAGCATGGAGCTTTGAATGCATATAAGTGCTAAAGAAAACAAAACA A T MRPL19 Ensembl:ENSG00000115364 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1414090921 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22478311,Human_RBP_ID_23886234 44595 RMVar_ID_44595 Human_SNP_ID_78187252 A-to-I Human chr2 - 75685607 75685607 75685607 GAGAAGGTAAGTGACCTGAATCCTGAGATACTATAGCACTGGGAAGTCAAAGAGATGACAAGCAG GAGAAGGTAAGTGACCTGAATCCTGAGATACTGTAGCACTGGGAAGTCAAAGAGATGACAAGCAG T C GCFC2 Ensembl:ENSG00000005436 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1370172293 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60219,RMVar_hsa_circ_74280,RMVar_hsa_circ_366376,RMVar_hsa_circ_371987,RMVar_hsa_circ_201416,RMVar_hsa_circ_1714,RMVar_hsa_circ_201415,RMVar_hsa_circ_364874,RMVar_hsa_circ_357111,RMVar_hsa_circ_324405,RMVar_hsa_circ_357532,RMVar_hsa_circ_54146,RMVar_hsa_circ_201417,RMVar_hsa_circ_362115,RMVar_hsa_circ_367302,RMVar_hsa_circ_67312 44596 RMVar_ID_44596 Human_SNP_ID_78187500 A-to-I Human chr2 - 75686662 75686662 75686662 ATTGCTCAAGTCAGTCTTGAATTCCTGGGGTCAAGTGATCCTACTGCCTCAGCCTCCCAATTAGC ATTGCTCAAGTCAGTCTTGAATTCCTGGGGTCGAGTGATCCTACTGCCTCAGCCTCCCAATTAGC T C GCFC2 Ensembl:ENSG00000005436 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs916380495 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60219,RMVar_hsa_circ_74280,RMVar_hsa_circ_366376,RMVar_hsa_circ_371987,RMVar_hsa_circ_201416,RMVar_hsa_circ_1714,RMVar_hsa_circ_201415,RMVar_hsa_circ_364874,RMVar_hsa_circ_357111,RMVar_hsa_circ_324405,RMVar_hsa_circ_357532,RMVar_hsa_circ_54146,RMVar_hsa_circ_201417,RMVar_hsa_circ_362115,RMVar_hsa_circ_367302,RMVar_hsa_circ_67312 44597 RMVar_ID_44597 Human_SNP_ID_78187519 A-to-I Human chr2 - 75686738 75686738 75686738 TATTTAATTTTTTGTGTGTTTGTTTTTGAGACAGGGTCTTCCTCTGTCACCCAGACTGGAGTACA TATTTAATTTTTTGTGTGTTTGTTTTTGAGACTGGGTCTTCCTCTGTCACCCAGACTGGAGTACA T A GCFC2 Ensembl:ENSG00000005436 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs538385961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569768 RMVar_hsa_circ_60219,RMVar_hsa_circ_74280,RMVar_hsa_circ_366376,RMVar_hsa_circ_371987,RMVar_hsa_circ_201416,RMVar_hsa_circ_1714,RMVar_hsa_circ_201415,RMVar_hsa_circ_364874,RMVar_hsa_circ_357111,RMVar_hsa_circ_324405,RMVar_hsa_circ_357532,RMVar_hsa_circ_54146,RMVar_hsa_circ_201417,RMVar_hsa_circ_362115,RMVar_hsa_circ_367302,RMVar_hsa_circ_67312 44598 RMVar_ID_44598 Human_SNP_ID_78187659 A-to-I Human chr2 - 75687195 75687195 75687195 GTGGTGGTTCATGCCTGTAATCCTGGAACTTTAGGAGGCCAAGGCAGGTAGATCACCTGAGGTCA GTGGTGGTTCATGCCTGTAATCCTGGAACTTTGGGAGGCCAAGGCAGGTAGATCACCTGAGGTCA T C GCFC2 Ensembl:ENSG00000005436 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1212669199 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20605128,Human_RBP_ID_21934803 RMVar_hsa_circ_60219,RMVar_hsa_circ_74280,RMVar_hsa_circ_366376,RMVar_hsa_circ_371987,RMVar_hsa_circ_201416,RMVar_hsa_circ_1714,RMVar_hsa_circ_201415,RMVar_hsa_circ_364874,RMVar_hsa_circ_357111,RMVar_hsa_circ_324405,RMVar_hsa_circ_357532,RMVar_hsa_circ_54146,RMVar_hsa_circ_201417,RMVar_hsa_circ_362115,RMVar_hsa_circ_367302,RMVar_hsa_circ_67312 44599 RMVar_ID_44599 Human_SNP_ID_78187702 A-to-I Human chr2 - 75687391 75687391 75687391 TACCTTCTCTGTTCTATTTACTTCAGTCACTTAGTATTTAAAGTCAGTTTAGTGTTTGTGGCATT TACCTTCTCTGTTCTATTTACTTCAGTCACTTCGTATTTAAAGTCAGTTTAGTGTTTGTGGCATT T G GCFC2 Ensembl:ENSG00000005436 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs565177174 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60219,RMVar_hsa_circ_74280,RMVar_hsa_circ_366376,RMVar_hsa_circ_371987,RMVar_hsa_circ_201416,RMVar_hsa_circ_1714,RMVar_hsa_circ_201415,RMVar_hsa_circ_364874,RMVar_hsa_circ_357111,RMVar_hsa_circ_324405,RMVar_hsa_circ_357532,RMVar_hsa_circ_54146,RMVar_hsa_circ_201417,RMVar_hsa_circ_362115,RMVar_hsa_circ_367302,RMVar_hsa_circ_67312 44600 RMVar_ID_44600 Human_SNP_ID_78187707 A-to-I Human chr2 + 75687418 75687418 75687418 AATACTAAGTGACTGAAGTAAATAGAACAGAGAAGGTAAGTGACCTGAATCCAGAGATACTGTAG AATACTAAGTGACTGAAGTAAATAGAACAGAGGAGGTAAGTGACCTGAATCCAGAGATACTGTAG A G MRPL19 Ensembl:ENSG00000115364 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1022959653 Functional Loss SNV dbSNP153 33..33 33 - - - 44601 RMVar_ID_44601 Human_SNP_ID_78187708 A-to-I Human chr2 + 75687418 75687418 75687418 AATACTAAGTGACTGAAGTAAATAGAACAGAGAAGGTAAGTGACCTGAATCCAGAGATACTGTAG AATACTAAGTGACTGAAGTAAATAGAACAGAGTAGGTAAGTGACCTGAATCCAGAGATACTGTAG A T MRPL19 Ensembl:ENSG00000115364 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1022959653 Functional Loss SNV dbSNP153 33..33 33 - - - 44602 RMVar_ID_44602 Human_SNP_ID_78187718 A-to-I Human chr2 - 75687454 75687454 75687454 TTGCTGTCTGCTTGTCACCTCTTTGACTTCCAAGTGCTACAGTATCTCTGGATTCAGGTCACTTA TTGCTGTCTGCTTGTCACCTCTTTGACTTCCAGGTGCTACAGTATCTCTGGATTCAGGTCACTTA T C GCFC2 Ensembl:ENSG00000005436 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1275652675 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20623536 RMVar_hsa_circ_60219,RMVar_hsa_circ_74280,RMVar_hsa_circ_366376,RMVar_hsa_circ_371987,RMVar_hsa_circ_201416,RMVar_hsa_circ_1714,RMVar_hsa_circ_201415,RMVar_hsa_circ_364874,RMVar_hsa_circ_357111,RMVar_hsa_circ_324405,RMVar_hsa_circ_357532,RMVar_hsa_circ_54146,RMVar_hsa_circ_201417,RMVar_hsa_circ_362115,RMVar_hsa_circ_367302,RMVar_hsa_circ_67312 44603 RMVar_ID_44603 Human_SNP_ID_78190880 A-to-I Human chr2 - 75699756 75699756 75699756 CCTGAACAACACAGTGAGACCTGAACTCTACTAAAAACAAATAAAACTAGCCAGGCATGGTGGCG CCTGAACAACACAGTGAGACCTGAACTCTACTCAAAACAAATAAAACTAGCCAGGCATGGTGGCG T G GCFC2 Ensembl:ENSG00000005436 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886288405 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_142135,Human_RBP_ID_23282399 RMVar_hsa_circ_366376,RMVar_hsa_circ_371987,RMVar_hsa_circ_1714,RMVar_hsa_circ_201415,RMVar_hsa_circ_357111,RMVar_hsa_circ_357532,RMVar_hsa_circ_54146,RMVar_hsa_circ_201417,RMVar_hsa_circ_362115,RMVar_hsa_circ_67312,RMVar_hsa_circ_334387,RMVar_hsa_circ_283926,RMVar_hsa_circ_54248,RMVar_hsa_circ_67630,RMVar_hsa_circ_201419,RMVar_hsa_circ_201418,RMVar_hsa_circ_57061,RMVar_hsa_circ_356526,RMVar_hsa_circ_351402,RMVar_hsa_circ_72714 44604 RMVar_ID_44604 Human_SNP_ID_78190882 A-to-I Human chr2 - 75699759 75699759 75699759 CAGCCTGAACAACACAGTGAGACCTGAACTCTACTAAAAACAAATAAAACTAGCCAGGCATGGTG CAGCCTGAACAACACAGTGAGACCTGAACTCTTCTAAAAACAAATAAAACTAGCCAGGCATGGTG T A GCFC2 Ensembl:ENSG00000005436 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1004946748 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23282399 RMVar_hsa_circ_366376,RMVar_hsa_circ_371987,RMVar_hsa_circ_1714,RMVar_hsa_circ_201415,RMVar_hsa_circ_357111,RMVar_hsa_circ_357532,RMVar_hsa_circ_54146,RMVar_hsa_circ_201417,RMVar_hsa_circ_362115,RMVar_hsa_circ_67312,RMVar_hsa_circ_334387,RMVar_hsa_circ_283926,RMVar_hsa_circ_54248,RMVar_hsa_circ_67630,RMVar_hsa_circ_201419,RMVar_hsa_circ_201418,RMVar_hsa_circ_57061,RMVar_hsa_circ_356526,RMVar_hsa_circ_351402,RMVar_hsa_circ_72714 44605 RMVar_ID_44605 Human_SNP_ID_78190883 A-to-I Human chr2 - 75699759 75699759 75699759 CAGCCTGAACAACACAGTGAGACCTGAACTCTACTAAAAACAAATAAAACTAGCCAGGCATGGTG CAGCCTGAACAACACAGTGAGACCTGAACTCTCCTAAAAACAAATAAAACTAGCCAGGCATGGTG T G GCFC2 Ensembl:ENSG00000005436 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1004946748 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23282399 RMVar_hsa_circ_366376,RMVar_hsa_circ_371987,RMVar_hsa_circ_1714,RMVar_hsa_circ_201415,RMVar_hsa_circ_357111,RMVar_hsa_circ_357532,RMVar_hsa_circ_54146,RMVar_hsa_circ_201417,RMVar_hsa_circ_362115,RMVar_hsa_circ_67312,RMVar_hsa_circ_334387,RMVar_hsa_circ_283926,RMVar_hsa_circ_54248,RMVar_hsa_circ_67630,RMVar_hsa_circ_201419,RMVar_hsa_circ_201418,RMVar_hsa_circ_57061,RMVar_hsa_circ_356526,RMVar_hsa_circ_351402,RMVar_hsa_circ_72714 44606 RMVar_ID_44606 Human_SNP_ID_78543146 A-to-I Human chr2 - 76947972 76947972 76947972 TAAAAGCCCAGCTCAGAGCATGCAATTAAGAAAGATGCTTCAGTCCAGAGTAGAAGGGAGGAAAA TAAAAGCCCAGCTCAGAGCATGCAATTAAGAAGGATGCTTCAGTCCAGAGTAGAAGGGAGGAAAA T C LRRTM4 Ensembl:ENSG00000176204 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1558756416 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_201425 44607 RMVar_ID_44607 Human_SNP_ID_78544550 A-to-I Human chr2 - 76952790 76952790 76952790 CCACACCCAGTCCCCCACACTGGCGGACATCGAGATTGGTACCATGTTTTTGCTATTGTGAATAA CCACACCCAGTCCCCCACACTGGCGGACATCGGGATTGGTACCATGTTTTTGCTATTGTGAATAA T C LRRTM4 Ensembl:ENSG00000176204 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs897888150 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_201425 44608 RMVar_ID_44608 Human_SNP_ID_78559190 A-to-I Human chr2 - 76998474 76998474 76998474 TGTGTGTTGGGGAGGGGTGGTGTGTGTGCATCATGGATCTGTTTGTTTAAGCAGCACTCAAATTG TGTGTGTTGGGGAGGGGTGGTGTGTGTGCATCTTGGATCTGTTTGTTTAAGCAGCACTCAAATTG T A LRRTM4 Ensembl:ENSG00000176204 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1422466938 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_201425 44609 RMVar_ID_44609 Human_SNP_ID_78559462 A-to-I Human chr2 - 76999133 76999130 76999134 TATTATAATCAATTTCAGTGCTGCTTAAACAAACAGATCCATGATGCACACACACTACCCCTCCC TATTATAATCAATTTCAGTGCTGCTTAAACA____GATCCATGATGCACACACACTACCCCTCCC CTGTT C LRRTM4 Ensembl:ENSG00000176204 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs201198509 Functional Loss DEL dbSNP153 32..35 33 - - - RMVar_hsa_circ_201425 44610 RMVar_ID_44610 Human_SNP_ID_78567444 A-to-I Human chr2 - 77023454 77023454 77023454 AGTTGAGAAAATTTGCAGCCTGACAATGTGGTAGAAAAGAAAATTCCATTTTCTGAGGAAATATT AGTTGAGAAAATTTGCAGCCTGACAATGTGGTGGAAAAGAAAATTCCATTTTCTGAGGAAATATT T C LRRTM4 Ensembl:ENSG00000176204 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1248637921 Functional Loss SNV dbSNP153 33..33 33 - - - 44611 RMVar_ID_44611 Human_SNP_ID_78574671 A-to-I Human chr2 - 77045721 77045721 77045721 TAATTGGACTTACAGTTCCATGTGGCTGGAGAAGCCTCACAATCATGGTGGAAGGCAAGGAGGAG TAATTGGACTTACAGTTCCATGTGGCTGGAGAGGCCTCACAATCATGGTGGAAGGCAAGGAGGAG T C LRRTM4 Ensembl:ENSG00000176204 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1324888902 Functional Loss SNV dbSNP153 33..33 33 - - - 44612 RMVar_ID_44612 Human_SNP_ID_78620488 A-to-I Human chr2 - 77196559 77196559 77196559 TTGTATTTTTAGTAAAGGTGAGGTTTCGCCATATTGGCCAGGAGGATCTTGAACTCCTGACCTTA TTGTATTTTTAGTAAAGGTGAGGTTTCGCCATGTTGGCCAGGAGGATCTTGAACTCCTGACCTTA T C LRRTM4 Ensembl:ENSG00000176204 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs532491972 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25566517 44613 RMVar_ID_44613 Human_SNP_ID_78633230 A-to-I Human chr2 - 77242875 77242875 77242875 TTTCAAGACCACTCTAACAGTTACTTGTAGGTATATACCTAGAAGTGGAATTCTTGGATTATAGG TTTCAAGACCACTCTAACAGTTACTTGTAGGTGTATACCTAGAAGTGGAATTCTTGGATTATAGG T C LRRTM4,AC013716.1 Ensembl:ENSG00000176204,Ensembl:ENSG00000286932 Protein coding,lincRNA intron,intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs576695176 Functional Loss SNV dbSNP153 33..33 33 - - - 44614 RMVar_ID_44614 Human_SNP_ID_78633254 A-to-I Human chr2 - 77242939 77242939 77242939 GGGTTGTTTCCACCTTTTGGCTATTCTGAATAATGCTGCTATGAACACGGGTGTATAGATACTTT GGGTTGTTTCCACCTTTTGGCTATTCTGAATACTGCTGCTATGAACACGGGTGTATAGATACTTT T G LRRTM4,AC013716.1 Ensembl:ENSG00000176204,Ensembl:ENSG00000286932 Protein coding,lincRNA intron,intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1558649576 Functional Loss SNV dbSNP153 33..33 33 - - - 44615 RMVar_ID_44615 Human_SNP_ID_78639418 A-to-I Human chr2 - 77265358 77265358 77265358 CAGAATACTAGCATTAATTTGTTTATGAGGGCAGAGACCTCATGACTGAATTATCTCTTCAAGTT CAGAATACTAGCATTAATTTGTTTATGAGGGCGGAGACCTCATGACTGAATTATCTCTTCAAGTT T C LRRTM4,AC013716.1 Ensembl:ENSG00000176204,Ensembl:ENSG00000286932 Protein coding,lincRNA intron,intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs767153188 Functional Loss SNV dbSNP153 33..33 33 - - - 44616 RMVar_ID_44616 Human_SNP_ID_78639461 A-to-I Human chr2 - 77265564 77265564 77265564 ATGCCACAGATGGATAATTTATAATAAACAGAAATTTATTTGGCTCATGGTTCTGGAGGCTGGGA ATGCCACAGATGGATAATTTATAATAAACAGAGATTTATTTGGCTCATGGTTCTGGAGGCTGGGA T C LRRTM4,AC013716.1 Ensembl:ENSG00000176204,Ensembl:ENSG00000286932 Protein coding,lincRNA intron,intron GSE107867 ASD brains,frontal_cortex;ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1437525305 Functional Loss SNV dbSNP153 33..33 33 - - - 44617 RMVar_ID_44617 Human_SNP_ID_78639855 A-to-I Human chr2 - 77267321 77267321 77267321 GTGCCTTGATCTTATACTAGAGGGCCTCCGGAACCATGAGAAAGAAAGCTCTATTGTTATAAATT GTGCCTTGATCTTATACTAGAGGGCCTCCGGAGCCATGAGAAAGAAAGCTCTATTGTTATAAATT T C LRRTM4,AC013716.1 Ensembl:ENSG00000176204,Ensembl:ENSG00000286932 Protein coding,lincRNA intron,intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1325873611 Functional Loss SNV dbSNP153 33..33 33 - - - 44618 RMVar_ID_44618 Human_SNP_ID_78656386 A-to-I Human chr2 - 77329373 77329373 77329373 GGATAAATTGCCATCCAAAACCATATTTACAAAGAATTTTAATGATGTAAGGAAATTCCCAGAAG GGATAAATTGCCATCCAAAACCATATTTACAAGGAATTTTAATGATGTAAGGAAATTCCCAGAAG T C LRRTM4 Ensembl:ENSG00000176204 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs992423025 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9111649 44619 RMVar_ID_44619 Human_SNP_ID_78680115 A-to-I Human chr2 - 77421002 77421001 77421002 TCTTTCAAGCTAATTTTTTATATTTTCTGCCCAGGCCTGTGGCCCACTATTTCTCCAAGGAGCCT TCTTTCAAGCTAATTTTTTATATTTTCTGCCC_GGCCTGTGGCCCACTATTTCTCCAAGGAGCCT CT C LRRTM4 Ensembl:ENSG00000176204 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1207212120 Functional Loss DEL dbSNP153 33..33 33 - - - 44620 RMVar_ID_44620 Human_SNP_ID_78684183 A-to-I Human chr2 - 77435812 77435812 77435812 ATATTGATGAATGAATATATAACTGAAGCTATATGAAGGTTTTGTGTCCACCTCCTACCTTAGAG ATATTGATGAATGAATATATAACTGAAGCTATGTGAAGGTTTTGTGTCCACCTCCTACCTTAGAG T C LRRTM4 Ensembl:ENSG00000176204 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs565269087 Functional Loss SNV dbSNP153 33..33 33 - - - 44621 RMVar_ID_44621 Human_SNP_ID_78688836 A-to-I Human chr2 - 77453346 77453346 77453346 GAACCCCGTCTCTACTAAAAATACAAAAAATTAGCCAGGCGTGGTGGTGGGCGCCTGTGGTCCCA GAACCCCGTCTCTACTAAAAATACAAAAAATTTGCCAGGCGTGGTGGTGGGCGCCTGTGGTCCCA T A LRRTM4 Ensembl:ENSG00000176204 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1459554792 Functional Loss SNV dbSNP153 33..33 33 - - - 44622 RMVar_ID_44622 Human_SNP_ID_78697146 A-to-I Human chr2 - 77482878 77482878 77482878 GACCTTGTGATCTGCCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCACGCC GACCTTGTGATCTGCCTGCCTCAGCCTCCCAACGTGCTGGGATTACAGGTGTGAGCCACCACGCC T G LRRTM4 Ensembl:ENSG00000176204 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1394170302 Functional Loss SNV dbSNP153 33..33 33 - - - 44623 RMVar_ID_44623 Human_SNP_ID_78697344 A-to-I Human chr2 - 77483401 77483401 77483401 GGGAGGCAGAGGTTGCAGTGAGCAGAGATCATACCATTGCACTCCAGCATGGGCTACAGAGAGAG GGGAGGCAGAGGTTGCAGTGAGCAGAGATCATGCCATTGCACTCCAGCATGGGCTACAGAGAGAG T C LRRTM4 Ensembl:ENSG00000176204 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank;ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1222440335 Functional Loss SNV dbSNP153 33..33 33 - - - 44624 RMVar_ID_44624 Human_SNP_ID_78704819 A-to-I Human chr2 - 77513792 77513792 77513792 GGAGGCCAAAGTGGGTGGATTACTTGAGGTCAAGAGTTTTAGACCAGTCTGACCAACATGGTGAA GGAGGCCAAAGTGGGTGGATTACTTGAGGTCAGGAGTTTTAGACCAGTCTGACCAACATGGTGAA T C LRRTM4 Ensembl:ENSG00000176204 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1245518604 Functional Loss SNV dbSNP153 33..33 33 - - - 44625 RMVar_ID_44625 Human_SNP_ID_78780708 A-to-I Human chr2 - 77792794 77792794 77792794 AGGCATGGCGACGAGGCGAACTGGGAGCTGGCACGGACCGGGACAGCGAGCAGCAACCGGGAAAA AGGCATGGCGACGAGGCGAACTGGGAGCTGGCGCGGACCGGGACAGCGAGCAGCAACCGGGAAAA T C AC012494.1 Ensembl:ENSG00000227088 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs967084086 Functional Loss SNV dbSNP153 33..33 33 - - - 44626 RMVar_ID_44626 Human_SNP_ID_78780714 A-to-I Human chr2 - 77792807 77792807 77792807 CCTCAATTTTCCGAGGCATGGCGACGAGGCGAACTGGGAGCTGGCACGGACCGGGACAGCGAGCA CCTCAATTTTCCGAGGCATGGCGACGAGGCGAGCTGGGAGCTGGCACGGACCGGGACAGCGAGCA T C AC012494.1 Ensembl:ENSG00000227088 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs916380676 Functional Loss SNV dbSNP153 33..33 33 - - - 44627 RMVar_ID_44627 Human_SNP_ID_78780728 A-to-I Human chr2 - 77792850 77792850 77792850 TTGGCATCCTTTCATCGGACTGTGAGCAGAAAATCCTTGATTTCCTCAATTTTCCGAGGCATGGC TTGGCATCCTTTCATCGGACTGTGAGCAGAAAGTCCTTGATTTCCTCAATTTTCCGAGGCATGGC T C AC012494.1 Ensembl:ENSG00000227088 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs901412672 Functional Loss SNV dbSNP153 33..33 33 - - - 44628 RMVar_ID_44628 Human_SNP_ID_78780729 A-to-I Human chr2 - 77792853 77792853 77792853 GATTTGGCATCCTTTCATCGGACTGTGAGCAGAAAATCCTTGATTTCCTCAATTTTCCGAGGCAT GATTTGGCATCCTTTCATCGGACTGTGAGCAGGAAATCCTTGATTTCCTCAATTTTCCGAGGCAT T C AC012494.1 Ensembl:ENSG00000227088 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs998402540 Functional Loss SNV dbSNP153 33..33 33 - - - 44629 RMVar_ID_44629 Human_SNP_ID_78780734 A-to-I Human chr2 - 77792864 77792864 77792864 TGATCTTGACGGATTTGGCATCCTTTCATCGGACTGTGAGCAGAAAATCCTTGATTTCCTCAATT TGATCTTGACGGATTTGGCATCCTTTCATCGGGCTGTGAGCAGAAAATCCTTGATTTCCTCAATT T C AC012494.1 Ensembl:ENSG00000227088 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1011091111 Functional Loss SNV dbSNP153 33..33 33 - - - 44630 RMVar_ID_44630 Human_SNP_ID_78780738 A-to-I Human chr2 - 77792869 77792869 77792869 TTTCTTGATCTTGACGGATTTGGCATCCTTTCATCGGACTGTGAGCAGAAAATCCTTGATTTCCT TTTCTTGATCTTGACGGATTTGGCATCCTTTCGTCGGACTGTGAGCAGAAAATCCTTGATTTCCT T C AC012494.1 Ensembl:ENSG00000227088 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978494620 Functional Loss SNV dbSNP153 33..33 33 - - - 44631 RMVar_ID_44631 Human_SNP_ID_78780748 A-to-I Human chr2 - 77792913 77792913 77792913 AGGTATTTGCTGTGTCAAACTTTAAACTTCACATTGTCCTTATTTTTCTTGATCTTGACGGATTT AGGTATTTGCTGTGTCAAACTTTAAACTTCACGTTGTCCTTATTTTTCTTGATCTTGACGGATTT T C AC012494.1 Ensembl:ENSG00000227088 lincRNA intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs990659705 Functional Loss SNV dbSNP153 33..33 33 - - - 44632 RMVar_ID_44632 Human_SNP_ID_79337132 A-to-I Human chr2 + 79916891 79916891 79916891 GTGATCCGCCCAACTTGGCCTCTCAAAGTGCTAGGATTACAGGCTTGAGCCGCTGTGCCCAGCTT GTGATCCGCCCAACTTGGCCTCTCAAAGTGCTGGGATTACAGGCTTGAGCCGCTGTGCCCAGCTT A G CTNNA2 Ensembl:ENSG00000066032 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1001758599 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40505,RMVar_hsa_circ_35302,RMVar_hsa_circ_201455,RMVar_hsa_circ_201454 44633 RMVar_ID_44633 Human_SNP_ID_79355870 A-to-I Human chr2 + 79989422 79989422 79989422 TAGTGGGTGGATCACTTGAGCCTAGAAGTTCAAAACCAGCCTGAGCAACATGGTGAAAATCCCGT TAGTGGGTGGATCACTTGAGCCTAGAAGTTCACAACCAGCCTGAGCAACATGGTGAAAATCCCGT A C CTNNA2 Ensembl:ENSG00000066032 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1365024209 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40505,RMVar_hsa_circ_35302,RMVar_hsa_circ_201455,RMVar_hsa_circ_201454 44634 RMVar_ID_44634 Human_SNP_ID_79364197 A-to-I Human chr2 + 80022582 80022582 80022582 GGGGCAGGAGTTTAGACCAGCTTGGGCAACATAGTGAGACCTTATCTTTACAAAAATAAAGTTAA GGGGCAGGAGTTTAGACCAGCTTGGGCAACATGGTGAGACCTTATCTTTACAAAAATAAAGTTAA A G CTNNA2 Ensembl:ENSG00000066032 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs544990053 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40505,RMVar_hsa_circ_35302 44635 RMVar_ID_44635 Human_SNP_ID_79366812 A-to-I Human chr2 + 80033012 80033012 80033012 ATCTCTACCAAAAATACAAAAATTAACTGGGCATGGTGGTGGGCGCCTGTAGTCCCAGATACTCA ATCTCTACCAAAAATACAAAAATTAACTGGGCTTGGTGGTGGGCGCCTGTAGTCCCAGATACTCA A T CTNNA2 Ensembl:ENSG00000066032 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs575638563 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40505,RMVar_hsa_circ_35302 44636 RMVar_ID_44636 Human_SNP_ID_80016575 A-to-I Human chr2 + 82609948 82609947 82609949 TCAGAACACCACAGGTATGTCCATTGGACAACAAAGAGTGAGAATTCCAAAAGTATGGGCACTAG TCAGAACACCACAGGTATGTCCATTGGACAAC__AGAGTGAGAATTCCAAAAGTATGGGCACTAG CAA C AC109638.1 Ensembl:ENSG00000226860 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1001988805 Functional Loss DEL dbSNP153 33..34 33 - - - 44637 RMVar_ID_44637 Human_SNP_ID_80467996 A-to-I Human chr2 - 84443360 84443360 84443360 TCACAGCCAGCAGGCATTGGAATATGGCACCAAACTCGTTGGAGGAACCACTCCAGGGAAAGGAG TCACAGCCAGCAGGCATTGGAATATGGCACCAGACTCGTTGGAGGAACCACTCCAGGGAAAGGAG T C SUCLG1 Ensembl:ENSG00000163541 Protein coding CDS GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831 HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line - 29129909,32596459 RNA-Seq:(High) rs564792232 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_5379569,Human_RBP_ID_8234403,Human_RBP_ID_13970044,Human_RBP_ID_17392729,Human_RBP_ID_18999756,Human_RBP_ID_22451434,Human_RBP_ID_22996992 Human_Splice_Rec_267504,Human_Splice_Rec_267505,Human_Splice_Rec_267522,Human_Splice_Rec_267523,Human_Splice_Rec_267554,Human_Splice_Rec_267555,Human_Splice_Rec_267564,Human_Splice_Rec_267565,Human_Splice_Rec_267572,Human_Splice_Rec_267573,Human_Splice_Rec_267578 Human_miRNA_ID_2057192 Clinvar_Rec_125 RMVar_hsa_circ_4713,RMVar_hsa_circ_346539,RMVar_hsa_circ_91999,RMVar_hsa_circ_113654,RMVar_hsa_circ_201484,RMVar_hsa_circ_281322,RMVar_hsa_circ_339375,RMVar_hsa_circ_201485,RMVar_hsa_circ_333200,RMVar_hsa_circ_201487,RMVar_hsa_circ_60972,RMVar_hsa_circ_201486 44638 RMVar_ID_44638 Human_SNP_ID_80467997 A-to-I Human chr2 - 84443360 84443360 84443360 TCACAGCCAGCAGGCATTGGAATATGGCACCAAACTCGTTGGAGGAACCACTCCAGGGAAAGGAG TCACAGCCAGCAGGCATTGGAATATGGCACCACACTCGTTGGAGGAACCACTCCAGGGAAAGGAG T G SUCLG1 Ensembl:ENSG00000163541 Protein coding CDS GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831 HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line - 29129909,32596459 RNA-Seq:(High) rs564792232 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5379569,Human_RBP_ID_8234403,Human_RBP_ID_13970044,Human_RBP_ID_17392729,Human_RBP_ID_18999756,Human_RBP_ID_22451434,Human_RBP_ID_22996992 Human_Splice_Rec_267504,Human_Splice_Rec_267505,Human_Splice_Rec_267522,Human_Splice_Rec_267523,Human_Splice_Rec_267554,Human_Splice_Rec_267555,Human_Splice_Rec_267564,Human_Splice_Rec_267565,Human_Splice_Rec_267572,Human_Splice_Rec_267573,Human_Splice_Rec_267578 Human_miRNA_ID_2057192 Clinvar_Rec_125 RMVar_hsa_circ_4713,RMVar_hsa_circ_346539,RMVar_hsa_circ_91999,RMVar_hsa_circ_113654,RMVar_hsa_circ_201484,RMVar_hsa_circ_281322,RMVar_hsa_circ_339375,RMVar_hsa_circ_201485,RMVar_hsa_circ_333200,RMVar_hsa_circ_201487,RMVar_hsa_circ_60972,RMVar_hsa_circ_201486 44639 RMVar_ID_44639 Human_SNP_ID_80574223 A-to-I Human chr2 - 84898209 84898209 84898209 GTGATGGTCATCCAAGAATGTGAATTCACTTAATGCCGCTGAACTGTACACTTAAAAATATAAAT GTGATGGTCATCCAAGAATGTGAATTCACTTATTGCCGCTGAACTGTACACTTAAAAATATAAAT T A TRABD2A Ensembl:ENSG00000186854 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1267829214 Functional Loss SNV dbSNP153 33..33 33 - - - 44640 RMVar_ID_44640 Human_SNP_ID_80587294 A-to-I Human chr2 - 84950066 84950066 84950066 TCATTGCAGCCTTGAACTGCTGGACTCAAGCAATCCTCCTGCCTCAGCTTCCCGAGTAGCCGGGA TCATTGCAGCCTTGAACTGCTGGACTCAAGCAGTCCTCCTGCCTCAGCTTCCCGAGTAGCCGGGA T C lnc-TRABD2A-5,lnc-TRABD2A-5:2 RNACentral:URS0000D57E27,RNACentral:URS0000D5D482 lincRNA,lincRNA exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404246494 Functional Loss SNV dbSNP153 33..33 33 - - - 44641 RMVar_ID_44641 Human_SNP_ID_80591145 A-to-I Human chr2 - 84965653 84965653 84965653 GTGGTGGCACACACCTGTAATCCCCGCTACTCAGGAGACAGGAGAATTGCTTGAACCTGGAAGGC GTGGTGGCACACACCTGTAATCCCCGCTACTCCGGAGACAGGAGAATTGCTTGAACCTGGAAGGC T G lnc-TRABD2A-5,lnc-TRABD2A-5:2,lnc-TRABD2A-5:3,lnc-TRABD2A-5:4,lnc-TRABD2A-5:5 RNACentral:URS0000D57E27,RNACentral:URS0000D58088,RNACentral:URS0000D591F9,RNACentral:URS0000D58ECF,RNACentral:URS0000D5D482 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,exon,exon,intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs988422579 Functional Loss SNV dbSNP153 33..33 33 - - - 44642 RMVar_ID_44642 Human_SNP_ID_80591236 A-to-I Human chr2 - 84965977 84965977 84965977 TGGGGTTTTGCTGTGTTAGCCAGGCTGATCTCAAACTCCTGACCCGCCTTTGCTTCCCAGAGTGC TGGGGTTTTGCTGTGTTAGCCAGGCTGATCTCGAACTCCTGACCCGCCTTTGCTTCCCAGAGTGC 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 RNACentral:URS0000D57E27,RNACentral:URS0000D58088,RNACentral:URS00008C398E,RNACentral:URS0000D591F9,RNACentral:URS0000D58ECF,RNACentral:URS0000D5D482 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,exon,exon,exon,intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs970182434 Functional Loss SNV dbSNP153 33..33 33 - - - 44643 RMVar_ID_44643 Human_SNP_ID_80591360 A-to-I Human chr2 - 84966527 84966527 84966527 CCTCAGGTGATCCACCCACCTCAGCCTCCCAAAGTCCTGGGATTACAGCCATGAGCCACCAGGCC CCTCAGGTGATCCACCCACCTCAGCCTCCCAACGTCCTGGGATTACAGCCATGAGCCACCAGGCC T G lnc-TRABD2A-5,lnc-TRABD2A-5:2,lnc-TRABD2A-5:3,lnc-TRABD2A-5:4,lnc-TRABD2A-5:5,lnc-TRABD2A-5:6 RNACentral:URS0000D57E27,RNACentral:URS0000D58088,RNACentral:URS00008C398E,RNACentral:URS0000D591F9,RNACentral:URS0000D58ECF,RNACentral:URS0000D5D482 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,exon,exon,exon,intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251315386 Functional Loss SNV dbSNP153 33..33 33 - - - 44644 RMVar_ID_44644 Human_SNP_ID_80591383 A-to-I Human chr2 - 84966623 84966623 84966623 GGACTACAGGAGGGTGCCATGACGCCTGGCTAATTTTTGTATATTTAGTAGAGACGGGGTTTCAC GGACTACAGGAGGGTGCCATGACGCCTGGCTACTTTTTGTATATTTAGTAGAGACGGGGTTTCAC T G lnc-TRABD2A-5,lnc-TRABD2A-5:2,lnc-TRABD2A-5:3,lnc-TRABD2A-5:4,lnc-TRABD2A-5:5,lnc-TRABD2A-5:6 RNACentral:URS0000D57E27,RNACentral:URS0000D58088,RNACentral:URS00008C398E,RNACentral:URS0000D591F9,RNACentral:URS0000D58ECF,RNACentral:URS0000D5D482 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,exon,exon,exon,intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs975996351 Functional Loss SNV dbSNP153 33..33 33 - - - 44645 RMVar_ID_44645 Human_SNP_ID_80591384 A-to-I Human chr2 - 84966624 84966624 84966624 GGGACTACAGGAGGGTGCCATGACGCCTGGCTAATTTTTGTATATTTAGTAGAGACGGGGTTTCA GGGACTACAGGAGGGTGCCATGACGCCTGGCTTATTTTTGTATATTTAGTAGAGACGGGGTTTCA T A lnc-TRABD2A-5,lnc-TRABD2A-5:2,lnc-TRABD2A-5:3,lnc-TRABD2A-5:4,lnc-TRABD2A-5:5,lnc-TRABD2A-5:6 RNACentral:URS0000D57E27,RNACentral:URS0000D58088,RNACentral:URS00008C398E,RNACentral:URS0000D591F9,RNACentral:URS0000D58ECF,RNACentral:URS0000D5D482 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,exon,exon,exon,intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1247151368 Functional Loss SNV dbSNP153 33..33 33 - - - 44646 RMVar_ID_44646 Human_SNP_ID_80591392 A-to-I Human chr2 - 84966650 84966650 84966650 CTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGAGGGTGCCATGACGCCTGGCTAATTTTT CTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTGCAGGAGGGTGCCATGACGCCTGGCTAATTTTT 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 RNACentral:URS0000D57E27,RNACentral:URS0000D58088,RNACentral:URS00008C398E,RNACentral:URS0000D591F9,RNACentral:URS0000D58ECF,RNACentral:URS0000D5D482 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,exon,exon,exon,intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005876077 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6953418 44647 RMVar_ID_44647 Human_SNP_ID_80591432 A-to-I Human chr2 - 84966766 84966766 84966766 ATTTATTTATTTATTTATTTATTTTTTGAGACAGAGCCTCTCTCTGTCGCACAGGCAGGAGTGCA ATTTATTTATTTATTTATTTATTTTTTGAGACGGAGCCTCTCTCTGTCGCACAGGCAGGAGTGCA 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 RNACentral:URS0000D57E27,RNACentral:URS0000D58088,RNACentral:URS00008C398E,RNACentral:URS0000D591F9,RNACentral:URS0000D58ECF,RNACentral:URS0000D5D482 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,exon,exon,exon,intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1259451708 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6976709,Human_RBP_ID_13970468 44648 RMVar_ID_44648 Human_SNP_ID_80591900 A-to-I Human chr2 - 84968478 84968478 84968478 TGATTGTACCACCACATCCTAGTCTGAGTGACAGTGTGACACTCTGTCTCAAAAAAGAAAAGAAG TGATTGTACCACCACATCCTAGTCTGAGTGACCGTGTGACACTCTGTCTCAAAAAAGAAAAGAAG T G 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:URS0000D58088,RNACentral:URS00008C398E,RNACentral:URS0000D591F9,RNACentral:URS00009B79DF,RNACentral:URS0000D5D245,RNACentral:URS0000D58ECF,RNACentral:URS0000D5D482 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,exon,exon,intron,intron,exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1482171096 Functional Loss SNV dbSNP153 33..33 33 - - - 44649 RMVar_ID_44649 Human_SNP_ID_80591958 A-to-I Human chr2 - 84968710 84968710 84968710 AAATTAGCCTGATGTGGTGGCACGCGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGAGAAC AAATTAGCCTGATGTGGTGGCACGCGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGAGAAC 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:URS0000D58088,RNACentral:URS00008C398E,RNACentral:URS0000D591F9,RNACentral:URS00009B79DF,RNACentral:URS0000D5D245,RNACentral:URS0000D58ECF,RNACentral:URS0000D5D482 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,exon,exon,exon,intron,exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs781061004 Functional Loss SNV dbSNP153 33..33 33 - - - 44650 RMVar_ID_44650 Human_SNP_ID_80601369 A-to-I Human chr2 + 85004326 85004326 85004326 GATGTCAGGAGATTGAGACTATCCTGGCTAACATGGTGAAAACCTGCCTCTACTAAAAGTACAAA GATGTCAGGAGATTGAGACTATCCTGGCTAACGTGGTGAAAACCTGCCTCTACTAAAAGTACAAA A G KCMF1 Ensembl:ENSG00000176407 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1410886851 Functional Loss SNV dbSNP153 33..33 33 - - - 44651 RMVar_ID_44651 Human_SNP_ID_80601438 A-to-I Human chr2 + 85004499 85004499 85004499 GCGCCACTGCACTCCAGCCTGGGCGACAGAGCAAGACTCCATCTCAAAAAAAAATAATAATAAAA GCGCCACTGCACTCCAGCCTGGGCGACAGAGCGAGACTCCATCTCAAAAAAAAATAATAATAAAA A G KCMF1 Ensembl:ENSG00000176407 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459536907 Functional Loss SNV dbSNP153 33..33 33 - - - 44652 RMVar_ID_44652 Human_SNP_ID_80602182 A-to-I Human chr2 + 85007058 85007058 85007058 GGGAGCCAGAGGTTGCAGTGAGTCGAGATCGCACCACTGCACTCCAGCCTGGGCAACAAGAGCAA GGGAGCCAGAGGTTGCAGTGAGTCGAGATCGCGCCACTGCACTCCAGCCTGGGCAACAAGAGCAA A G KCMF1 Ensembl:ENSG00000176407 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1190739697 Functional Loss SNV dbSNP153 33..33 33 - - - 44653 RMVar_ID_44653 Human_SNP_ID_80603063 A-to-I Human chr2 + 85008930 85008930 85008930 TGGCAGTTTTTTTGTAGATAGGAGGTCTTACTATATCGCCCTGGTTGGTCTCAAACTCTTGGGCT TGGCAGTTTTTTTGTAGATAGGAGGTCTTACTGTATCGCCCTGGTTGGTCTCAAACTCTTGGGCT A G KCMF1 Ensembl:ENSG00000176407 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1382280733 Functional Loss SNV dbSNP153 33..33 33 - - - 44654 RMVar_ID_44654 Human_SNP_ID_80607139 A-to-I Human chr2 + 85024350 85024350 85024350 CAAAAATTAGCTGGGCATGGTGCCAGGCGCCTATGATCCCAACTCCTTGGGAGGCTGAGGCAGGA CAAAAATTAGCTGGGCATGGTGCCAGGCGCCTGTGATCCCAACTCCTTGGGAGGCTGAGGCAGGA A G KCMF1 Ensembl:ENSG00000176407 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1001314824 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_293872 44655 RMVar_ID_44655 Human_SNP_ID_80611956 A-to-I Human chr2 + 85044428 85044428 85044428 TCGGAGTCTTGCTCTGTCAGCCAGGCTGGAGTACAATGGTGCTATCTTCAGCTTATTGCAACCTC TCGGAGTCTTGCTCTGTCAGCCAGGCTGGAGTGCAATGGTGCTATCTTCAGCTTATTGCAACCTC A G KCMF1 Ensembl:ENSG00000176407 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1453529587 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_201510,RMVar_hsa_circ_278040,RMVar_hsa_circ_292048,RMVar_hsa_circ_267616,RMVar_hsa_circ_201509,RMVar_hsa_circ_326616,RMVar_hsa_circ_329943,RMVar_hsa_circ_268601,RMVar_hsa_circ_201515,RMVar_hsa_circ_201511,RMVar_hsa_circ_201512,RMVar_hsa_circ_273267,RMVar_hsa_circ_282337,RMVar_hsa_circ_201516 44656 RMVar_ID_44656 Human_SNP_ID_80612638 A-to-I Human chr2 + 85047303 85047303 85047303 CATAAAAAAATGTCCAAAGCACATTTGAAATTAAGGTTTTATAAGGTATAGCTAACATTTTTAAG CATAAAAAAATGTCCAAAGCACATTTGAAATTTAGGTTTTATAAGGTATAGCTAACATTTTTAAG A T KCMF1 Ensembl:ENSG00000176407 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900987258 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_201510,RMVar_hsa_circ_278040,RMVar_hsa_circ_267616,RMVar_hsa_circ_326616,RMVar_hsa_circ_268601,RMVar_hsa_circ_201511,RMVar_hsa_circ_273267,RMVar_hsa_circ_201516,RMVar_hsa_circ_91309,RMVar_hsa_circ_201517 44657 RMVar_ID_44657 Human_SNP_ID_80626120 A-to-I Human chr2 + 85102456 85102456 85102456 ATCTCCCTGGACAAAAAGCATTGGAATATTCCATTTCATTGGTTTATATATCTCTTCATATGTTT ATCTCCCTGGACAAAAAGCATTGGAATATTCCGTTTCATTGGTTTATATATCTCTTCATATGTTT A G L13705-001 RNACentral:URS00005A0C9B misc_RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879091485 Functional Loss SNV dbSNP153 33..33 33 - - - 44658 RMVar_ID_44658 Human_SNP_ID_80626123 A-to-I Human chr2 + 85102461 85102461 85102461 CCTGGACAAAAAGCATTGGAATATTCCATTTCATTGGTTTATATATCTCTTCATATGTTTCTTCA CCTGGACAAAAAGCATTGGAATATTCCATTTCGTTGGTTTATATATCTCTTCATATGTTTCTTCA A G L13705-001 RNACentral:URS00005A0C9B misc_RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878965496 Functional Loss SNV dbSNP153 33..33 33 - - - 44659 RMVar_ID_44659 Human_SNP_ID_80636966 A-to-I Human chr2 + 85144974 85144974 85144974 GGGTGTGGTAGCACACACCTATAATCCCAGCTACTCGGGAGGCTGAGGCGGGAGAATTGCTTGGA GGGTGTGGTAGCACACACCTATAATCCCAGCTGCTCGGGAGGCTGAGGCGGGAGAATTGCTTGGA A G TCF7L1 Ensembl:ENSG00000152284 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1451829566 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23887127 44660 RMVar_ID_44660 Human_SNP_ID_80679064 A-to-I Human chr2 - 85319230 85319230 85319230 GAGGTTGCAGTGAGCCGAGATCGTGCCACTGAACTCCAACCTGCCAATAGAGCGAGACTCCGTCT GAGGTTGCAGTGAGCCGAGATCGTGCCACTGAGCTCCAACCTGCCAATAGAGCGAGACTCCGTCT T C TGOLN2 Ensembl:ENSG00000152291 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1132880 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8852634,Human_RBP_ID_13972184,Human_RBP_ID_17965411,Human_RBP_ID_26770262,Human_RBP_ID_27482070 44661 RMVar_ID_44661 Human_SNP_ID_80679091 A-to-I Human chr2 - 85319334 85319334 85319334 GTCTCTAATAAAAATACAAAAATTAGCCGGGCATGGTGACGTGCACCTGTAGTCCCAGCTACTAG GTCTCTAATAAAAATACAAAAATTAGCCGGGCGTGGTGACGTGCACCTGTAGTCCCAGCTACTAG T C TGOLN2 Ensembl:ENSG00000152291 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs11541449 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1097524 44662 RMVar_ID_44662 Human_SNP_ID_80679092 A-to-I Human chr2 - 85319334 85319334 85319334 GTCTCTAATAAAAATACAAAAATTAGCCGGGCATGGTGACGTGCACCTGTAGTCCCAGCTACTAG GTCTCTAATAAAAATACAAAAATTAGCCGGGCCTGGTGACGTGCACCTGTAGTCCCAGCTACTAG T G TGOLN2 Ensembl:ENSG00000152291 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs11541449 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1097524 44663 RMVar_ID_44663 Human_SNP_ID_80679100 A-to-I Human chr2 - 85319351 85319351 85319351 CAACATGGTGAAACCCCGTCTCTAATAAAAATACAAAAATTAGCCGGGCATGGTGACGTGCACCT CAACATGGTGAAACCCCGTCTCTAATAAAAATGCAAAAATTAGCCGGGCATGGTGACGTGCACCT T C TGOLN2 Ensembl:ENSG00000152291 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1138829 Functional Loss SNV dbSNP153 33..33 33 - - - 44664 RMVar_ID_44664 Human_SNP_ID_80679190 A-to-I Human chr2 - 85319761 85319761 85319761 TAGGACTTCCAGAGTTCAGTTCCTTCTGGCAGAGAGGTTTTCTTTCTCCATGCCATATGGATGTG TAGGACTTCCAGAGTTCAGTTCCTTCTGGCAGGGAGGTTTTCTTTCTCCATGCCATATGGATGTG T C TGOLN2 Ensembl:ENSG00000152291 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1470466103 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1590885,Human_RBP_ID_3635356,Human_RBP_ID_8850157,Human_RBP_ID_20606996,Human_RBP_ID_23232919 44665 RMVar_ID_44665 Human_SNP_ID_80679956 A-to-I Human chr2 - 85323132 85323132 85323132 GAAATACCATCTCTACTAAAAATACAAAAATTAGCTGGGCATGGTAATCCCAGCTACTACTGAGG GAAATACCATCTCTACTAAAAATACAAAAATTGGCTGGGCATGGTAATCCCAGCTACTACTGAGG T C TGOLN2 Ensembl:ENSG00000152291 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs936762725 Functional Loss SNV dbSNP153 33..33 33 - - - 44666 RMVar_ID_44666 Human_SNP_ID_80679959 A-to-I Human chr2 - 85323150 85323150 85323150 CAGTCTGGCCAACATGGTGAAATACCATCTCTACTAAAAATACAAAAATTAGCTGGGCATGGTAA CAGTCTGGCCAACATGGTGAAATACCATCTCTGCTAAAAATACAAAAATTAGCTGGGCATGGTAA T C TGOLN2 Ensembl:ENSG00000152291 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs907773657 Functional Loss SNV dbSNP153 33..33 33 - - - 44667 RMVar_ID_44667 Human_SNP_ID_80680020 A-to-I Human chr2 - 85323400 85323400 85323400 CACCACGCCCAGCTAATTTTTAGATTTTTAGTAGAGATGGGGTTTCACCCTTTTGGCCAGGCTGG CACCACGCCCAGCTAATTTTTAGATTTTTAGTGGAGATGGGGTTTCACCCTTTTGGCCAGGCTGG T C TGOLN2 Ensembl:ENSG00000152291 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1205770661 Functional Loss SNV dbSNP153 33..33 33 - - - 44668 RMVar_ID_44668 Human_SNP_ID_80680045 A-to-I Human chr2 - 85323483 85323483 85323483 TGGCTCACTGCAACCTCCACCACCCGGGTTCAAGCAGTTCTCCCTCTTCAGCCTCCCGAGTAGGT TGGCTCACTGCAACCTCCACCACCCGGGTTCAGGCAGTTCTCCCTCTTCAGCCTCCCGAGTAGGT T C TGOLN2 Ensembl:ENSG00000152291 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1220509711 Functional Loss SNV dbSNP153 33..33 33 - - - 44669 RMVar_ID_44669 Human_SNP_ID_80680046 A-to-I Human chr2 - 85323484 85323484 85323484 TTGGCTCACTGCAACCTCCACCACCCGGGTTCAAGCAGTTCTCCCTCTTCAGCCTCCCGAGTAGG TTGGCTCACTGCAACCTCCACCACCCGGGTTCGAGCAGTTCTCCCTCTTCAGCCTCCCGAGTAGG T C TGOLN2 Ensembl:ENSG00000152291 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs944277835 Functional Loss SNV dbSNP153 33..33 33 - - - 44670 RMVar_ID_44670 Human_SNP_ID_80680057 A-to-I Human chr2 - 85323519 85323519 85323519 CTGTGTCGTCCAGGCTGGAGTGCAGTGGCACAATCTTGGCTCACTGCAACCTCCACCACCCGGGT CTGTGTCGTCCAGGCTGGAGTGCAGTGGCACAGTCTTGGCTCACTGCAACCTCCACCACCCGGGT T C TGOLN2 Ensembl:ENSG00000152291 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs940961335 Functional Loss SNV dbSNP153 33..33 33 - - - 44671 RMVar_ID_44671 Human_SNP_ID_80680058 A-to-I Human chr2 - 85323520 85323520 85323520 GCTGTGTCGTCCAGGCTGGAGTGCAGTGGCACAATCTTGGCTCACTGCAACCTCCACCACCCGGG GCTGTGTCGTCCAGGCTGGAGTGCAGTGGCACGATCTTGGCTCACTGCAACCTCCACCACCCGGG T C TGOLN2 Ensembl:ENSG00000152291 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs758952309 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_147058 44672 RMVar_ID_44672 Human_SNP_ID_80680911 A-to-I Human chr2 - 85326828 85326828 85326828 CTCATGCTTTCAAAACCGAATCTGGGGAGGAAACTGACCTCATTTCTCCCCCGCAGGAGGAAGTT CTCATGCTTTCAAAACCGAATCTGGGGAGGAATCTGACCTCATTTCTCCCCCGCAGGAGGAAGTT T A TGOLN2 Ensembl:ENSG00000152291 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1185851051 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17962425,Human_RBP_ID_18766412,Human_RBP_ID_22669156,Human_RBP_ID_22765870,Human_RBP_ID_27482103 RMVar_hsa_circ_53992 44673 RMVar_ID_44673 Human_SNP_ID_80686743 A-to-I Human chr2 - 85346561 85346561 85346561 TAGAGACAGGGTCTCACTATGTTGCCCAGGCTAGTCTTGAACTCCTGTACACAAGCAATCAGTCC TAGAGACAGGGTCTCACTATGTTGCCCAGGCTGGTCTTGAACTCCTGTACACAAGCAATCAGTCC T C RETSAT Ensembl:ENSG00000042445 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1000923527 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_201523,RMVar_hsa_circ_76081,RMVar_hsa_circ_337375,RMVar_hsa_circ_201524 44674 RMVar_ID_44674 Human_SNP_ID_80686745 A-to-I Human chr2 - 85346575 85346575 85346575 ATTTTTTTGTTCTATAGAGACAGGGTCTCACTATGTTGCCCAGGCTAGTCTTGAACTCCTGTACA ATTTTTTTGTTCTATAGAGACAGGGTCTCACTGTGTTGCCCAGGCTAGTCTTGAACTCCTGTACA T C RETSAT Ensembl:ENSG00000042445 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1042711937 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_201523,RMVar_hsa_circ_76081,RMVar_hsa_circ_337375,RMVar_hsa_circ_201524 44675 RMVar_ID_44675 Human_SNP_ID_80687154 A-to-I Human chr2 - 85348441 85348441 85348441 TTTTTAGTAGAGATGGGGTTTCACCATGTGTTAGCCAGGATGGTCTCAATCTCCTGATCTTGTGA TTTTTAGTAGAGATGGGGTTTCACCATGTGTTGGCCAGGATGGTCTCAATCTCCTGATCTTGTGA T C RETSAT Ensembl:ENSG00000042445 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs568990554 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_201523,RMVar_hsa_circ_76081,RMVar_hsa_circ_337375,RMVar_hsa_circ_201524 44676 RMVar_ID_44676 Human_SNP_ID_80688457 A-to-I Human chr2 - 85353226 85353226 85353226 CTCTCGAACTCCTGGCCTCAAGCGATCCGCCCACCTCGGCCTCCCAAAGTGTTGGGATTACAGGC CTCTCGAACTCCTGGCCTCAAGCGATCCGCCCGCCTCGGCCTCCCAAAGTGTTGGGATTACAGGC T C RETSAT Ensembl:ENSG00000042445 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs972293237 Functional Loss SNV dbSNP153 33..33 33 - - - 44677 RMVar_ID_44677 Human_SNP_ID_80688500 A-to-I Human chr2 - 85353415 85353415 85353415 TTTATTTATTTATTGAAACAGAGTCTCGCTCTATTGTCCATGCTAGAGTGCAGTGGCGCGATCTC TTTATTTATTTATTGAAACAGAGTCTCGCTCTGTTGTCCATGCTAGAGTGCAGTGGCGCGATCTC T C RETSAT Ensembl:ENSG00000042445 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1434675804 Functional Loss SNV dbSNP153 33..33 33 - - - 44678 RMVar_ID_44678 Human_SNP_ID_80695034 A-to-I Human chr2 + 85380545 85380545 85380545 AGATGATGATTATTATTTATTTATTTATTTTTAGACTACTCTTGCTCTGTCGCGCAGGGTGAAGT AGATGATGATTATTATTTATTTATTTATTTTTGGACTACTCTTGCTCTGTCGCGCAGGGTGAAGT A G ELMOD3 Ensembl:ENSG00000115459 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388959544 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6953944 RMVar_hsa_circ_87682,RMVar_hsa_circ_353948,RMVar_hsa_circ_201526,RMVar_hsa_circ_112462,RMVar_hsa_circ_318213,RMVar_hsa_circ_374560,RMVar_hsa_circ_11087,RMVar_hsa_circ_24036,RMVar_hsa_circ_201531,RMVar_hsa_circ_201530,RMVar_hsa_circ_123409,RMVar_hsa_circ_67596,RMVar_hsa_circ_267501,RMVar_hsa_circ_201540 44679 RMVar_ID_44679 Human_SNP_ID_80695516 A-to-I Human chr2 + 85382546 85382544 85382547 ACAAGGACTTTTTTTTTTTGAGACAGAGTCTCACTTTTGTCACACAGGCTGGAGTGCAGTGGCGC ACAAGGACTTTTTTTTTTTGAGACAGAGTCT___TTTTGTCACACAGGCTGGAGTGCAGTGGCGC TCAC T ELMOD3 Ensembl:ENSG00000115459 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1405535925 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_87682,RMVar_hsa_circ_353948,RMVar_hsa_circ_201526,RMVar_hsa_circ_112462,RMVar_hsa_circ_318213,RMVar_hsa_circ_374560,RMVar_hsa_circ_11087,RMVar_hsa_circ_24036,RMVar_hsa_circ_201531,RMVar_hsa_circ_201530,RMVar_hsa_circ_123409,RMVar_hsa_circ_67596,RMVar_hsa_circ_267501,RMVar_hsa_circ_201540 44680 RMVar_ID_44680 Human_SNP_ID_80696358 A-to-I Human chr2 + 85386464 85386464 85386464 CTAGAATGCATGGCACAATCTCAACTCACTGCAACCTCTGCCTCCTGAGTTCAAGCGATTCTTCT CTAGAATGCATGGCACAATCTCAACTCACTGCGACCTCTGCCTCCTGAGTTCAAGCGATTCTTCT A G ELMOD3 Ensembl:ENSG00000115459 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1276682370 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87682,RMVar_hsa_circ_353948,RMVar_hsa_circ_201526,RMVar_hsa_circ_112462,RMVar_hsa_circ_318213,RMVar_hsa_circ_374560,RMVar_hsa_circ_11087,RMVar_hsa_circ_24036,RMVar_hsa_circ_201531,RMVar_hsa_circ_201530,RMVar_hsa_circ_123409,RMVar_hsa_circ_67596,RMVar_hsa_circ_267501,RMVar_hsa_circ_201540 44681 RMVar_ID_44681 Human_SNP_ID_80696368 A-to-I Human chr2 - 85386493 85386493 85386493 GTAATCCCAGCTACTTGGGAGGCTCAGGCAGAAGAATCGCTTGAACTCAGGAGGCAGAGGTTGCA GTAATCCCAGCTACTTGGGAGGCTCAGGCAGAGGAATCGCTTGAACTCAGGAGGCAGAGGTTGCA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs898605178 Functional Loss SNV dbSNP153 33..33 33 - - - 44682 RMVar_ID_44682 Human_SNP_ID_80735336 A-to-I Human chr2 + 85539201 85539201 85539201 TTCGCTCCGCGCCGCCCGCCTGCTACGAGTAGAACGCTGTCCGCAGCTTGCGCATTTCGCAGCCG TTCGCTCCGCGCCGCCCGCCTGCTACGAGTAGGACGCTGTCCGCAGCTTGCGCATTTCGCAGCCG A G MAT2A Ensembl:ENSG00000168906 Protein coding exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs989401149 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_243153,Human_RBP_ID_776449,Human_RBP_ID_829804,Human_RBP_ID_1590932,Human_RBP_ID_1924048,Human_RBP_ID_2666982,Human_RBP_ID_3635416,Human_RBP_ID_4634866,Human_RBP_ID_5445178,Human_RBP_ID_5589626,Human_RBP_ID_13972934,Human_RBP_ID_18766450 RMVar_hsa_circ_91716,RMVar_hsa_circ_201547 44683 RMVar_ID_44683 Human_SNP_ID_80737447 A-to-I Human chr2 - 85545396 85545396 85545396 GCTGGAGTGCAGTGGCTTGATAATGGTTCGCTACAGCCTCCAACTTCTATGTTAAAGTGATCCTC GCTGGAGTGCAGTGGCTTGATAATGGTTCGCTGCAGCCTCCAACTTCTATGTTAAAGTGATCCTC T C GGCX Ensembl:ENSG00000115486 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs575528704 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1024422 Clinvar_Rec_126 44684 RMVar_ID_44684 Human_SNP_ID_80737780 A-to-I Human chr2 - 85546267 85546266 85546268 AGGTGCCTGGCTAACTTTTTTATATTTTTAGTAGAGACAGGGTTTCACTGTGTTAGCCAGGATGG AGGTGCCTGGCTAACTTTTTTATATTTTTAG__GAGACAGGGTTTCACTGTGTTAGCCAGGATGG CTA C GGCX Ensembl:ENSG00000115486 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1193253596 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_146005 44685 RMVar_ID_44685 Human_SNP_ID_80737781 A-to-I Human chr2 - 85546267 85546267 85546267 AGGTGCCTGGCTAACTTTTTTATATTTTTAGTAGAGACAGGGTTTCACTGTGTTAGCCAGGATGG AGGTGCCTGGCTAACTTTTTTATATTTTTAGTGGAGACAGGGTTTCACTGTGTTAGCCAGGATGG T C GGCX Ensembl:ENSG00000115486 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1229491835 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_146005 44686 RMVar_ID_44686 Human_SNP_ID_80737786 A-to-I Human chr2 - 85546278 85546277 85546278 GCTGGGACTACAGGTGCCTGGCTAACTTTTTTATATTTTTAGTAGAGACAGGGTTTCACTGTGTT GCTGGGACTACAGGTGCCTGGCTAACTTTTTT_TATTTTTAGTAGAGACAGGGTTTCACTGTGTT AT A GGCX Ensembl:ENSG00000115486 Protein coding 3'UTR GSE47997;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 23474544,31158229,31158229 RNA-Seq:(High) rs1489272392 Functional Loss DEL dbSNP153 33..33 33 - - - 44687 RMVar_ID_44687 Human_SNP_ID_80737787 A-to-I Human chr2 - 85546278 85546278 85546278 GCTGGGACTACAGGTGCCTGGCTAACTTTTTTATATTTTTAGTAGAGACAGGGTTTCACTGTGTT GCTGGGACTACAGGTGCCTGGCTAACTTTTTTGTATTTTTAGTAGAGACAGGGTTTCACTGTGTT T C GGCX Ensembl:ENSG00000115486 Protein coding 3'UTR GSE47997;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 23474544,31158229,31158229 RNA-Seq:(High) rs1011429519 Functional Loss SNV dbSNP153 33..33 33 - - - 44688 RMVar_ID_44688 Human_SNP_ID_80737788 A-to-I Human chr2 - 85546278 85546278 85546278 GCTGGGACTACAGGTGCCTGGCTAACTTTTTTATATTTTTAGTAGAGACAGGGTTTCACTGTGTT GCTGGGACTACAGGTGCCTGGCTAACTTTTTTCTATTTTTAGTAGAGACAGGGTTTCACTGTGTT T G GGCX Ensembl:ENSG00000115486 Protein coding 3'UTR GSE47997;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 23474544,31158229,31158229 RNA-Seq:(High) rs1011429519 Functional Loss SNV dbSNP153 33..33 33 - - - 44689 RMVar_ID_44689 Human_SNP_ID_80737828 A-to-I Human chr2 - 85546354 85546354 85546354 TGGTGGCACGATTTCAGCTCACTGCAAGCTCCACCTCCCGGGTTCACGCCATTCTCCTGCCTCGG TGGTGGCACGATTTCAGCTCACTGCAAGCTCCGCCTCCCGGGTTCACGCCATTCTCCTGCCTCGG T C GGCX Ensembl:ENSG00000115486 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982221009 Functional Loss SNV dbSNP153 33..33 33 - - - 44690 RMVar_ID_44690 Human_SNP_ID_80737837 A-to-I Human chr2 - 85546371 85546371 85546371 TTACCCTGGCCGGAGTGTGGTGGCACGATTTCAGCTCACTGCAAGCTCCACCTCCCGGGTTCACG TTACCCTGGCCGGAGTGTGGTGGCACGATTTCGGCTCACTGCAAGCTCCACCTCCCGGGTTCACG T C GGCX Ensembl:ENSG00000115486 Protein coding 3'UTR GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 ASD brains,cerebellum;ASD brains,frontal_cortex;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 30559470,31158229,31158229 RNA-Seq:(High) rs1290744662 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_556641 44691 RMVar_ID_44691 Human_SNP_ID_80737962 A-to-I Human chr2 - 85546641 85546641 85546641 GGAGTGCAATGGCGCCATCTCGGCTCACTGCAACCTCTGCCTCCTGGGTTCAAGTGATTCTCCAG GGAGTGCAATGGCGCCATCTCGGCTCACTGCAGCCTCTGCCTCCTGGGTTCAAGTGATTCTCCAG T C GGCX Ensembl:ENSG00000115486 Protein coding 3'UTR GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1284844517 Functional Loss SNV dbSNP153 33..33 33 - - - 44692 RMVar_ID_44692 Human_SNP_ID_80737976 A-to-I Human chr2 - 85546665 85546665 85546665 AGGAACCTTGCTCTGGCCCAGGCTGGAGTGCAATGGCGCCATCTCGGCTCACTGCAACCTCTGCC AGGAACCTTGCTCTGGCCCAGGCTGGAGTGCAGTGGCGCCATCTCGGCTCACTGCAACCTCTGCC T C GGCX Ensembl:ENSG00000115486 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs563109158 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23887366 44693 RMVar_ID_44693 Human_SNP_ID_80738408 A-to-I Human chr2 - 85548075 85548075 85548075 CTTCCACTTCAGCCTCCCATGTAGCTGGGACTACAGGTGCCCACCACCACGCCCAACTAATTTTT CTTCCACTTCAGCCTCCCATGTAGCTGGGACTTCAGGTGCCCACCACCACGCCCAACTAATTTTT T A GGCX Ensembl:ENSG00000115486 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line - 31158229,32596459 RNA-Seq:(High) rs965551488 Functional Loss SNV dbSNP153 33..33 33 - - - 44694 RMVar_ID_44694 Human_SNP_ID_80748803 A-to-I Human chr2 + 85589114 85589114 85589114 CAAGACCATCCTGGGCAACATAGCAAGACCCCATCTTTAAAAATATAGGCACCATTTATTCAGGA CAAGACCATCCTGGGCAACATAGCAAGACCCCGTCTTTAAAAATATAGGCACCATTTATTCAGGA A G VAMP5 Ensembl:ENSG00000168899 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1558824683 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99210,RMVar_hsa_circ_201567 44695 RMVar_ID_44695 Human_SNP_ID_80754269 A-to-I Human chr2 - 85609849 85609849 85609849 TGGTAAAACCCCATCTCTACTAAAAATATGAAAATTAGCTGGATGTGGTGGCACTTGCCTGTAAT TGGTAAAACCCCATCTCTACTAAAAATATGAAGATTAGCTGGATGTGGTGGCACTTGCCTGTAAT T C C2orf68 Ensembl:ENSG00000168887 Protein coding intron GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459,32596459 RNA-Seq:(High) rs1358708060 Functional Loss SNV dbSNP153 33..33 33 - - - 44696 RMVar_ID_44696 Human_SNP_ID_80754368 A-to-I Human chr2 - 85610163 85610163 85610163 TAAAAATACAAAAATTAGCCAGGCATGATGGCAGGCGGCTGTAATCCCAGCTACTTGGGAGGCTG TAAAAATACAAAAATTAGCCAGGCATGATGGCGGGCGGCTGTAATCCCAGCTACTTGGGAGGCTG T C C2orf68 Ensembl:ENSG00000168887 Protein coding intron GSE38233;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;esophageal squamous carcinoma cells,EC109 cell line - 24183664,32596459 RNA-Seq:(High) rs1182802704 Functional Loss SNV dbSNP153 33..33 33 - - - 44697 RMVar_ID_44697 Human_SNP_ID_80754379 A-to-I Human chr2 - 85610216 85610216 85610216 GAGGCCAGGAGTTCGAAATTAACCTGGACAACATGGTGAAACCCCATCTCTACTAAAAATACAAA GAGGCCAGGAGTTCGAAATTAACCTGGACAACTTGGTGAAACCCCATCTCTACTAAAAATACAAA T A C2orf68 Ensembl:ENSG00000168887 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs979047373 Functional Loss SNV dbSNP153 33..33 33 - - - 44698 RMVar_ID_44698 Human_SNP_ID_80754676 A-to-I Human chr2 - 85611169 85611169 85611169 GACTAGGTCTCTGTCGCCCAGGCTGGAGTGCAATGGTGCGATCTGGGCTTACTGCAGCCTTAGCC GACTAGGTCTCTGTCGCCCAGGCTGGAGTGCAGTGGTGCGATCTGGGCTTACTGCAGCCTTAGCC T C C2orf68 Ensembl:ENSG00000168887 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1200053062 Functional Loss SNV dbSNP153 33..33 33 - - - 44699 RMVar_ID_44699 Human_SNP_ID_80759605 A-to-I Human chr2 + 85627280 85627280 85627280 CACCACACCCGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGG CACCACACCCGGCTAATTTTTGTATTTTTAGTGGAGATGGGGTTTCACCATGTTGGCCAGGCTGG A G USP39 Ensembl:ENSG00000168883 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1468372890 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_310,RMVar_hsa_circ_334819,RMVar_hsa_circ_347953,RMVar_hsa_circ_332846,RMVar_hsa_circ_283571,RMVar_hsa_circ_101891,RMVar_hsa_circ_27724,RMVar_hsa_circ_201580,RMVar_hsa_circ_39036,RMVar_hsa_circ_31899,RMVar_hsa_circ_201583,RMVar_hsa_circ_343914 44700 RMVar_ID_44700 Human_SNP_ID_80760965 A-to-I Human chr2 + 85632333 85632333 85632333 GTCTGAGCTACTTGGGAGGCTGAGGCAGGAGTATTGCTTGAGCCCAGGAGTTCAAGGCTACAGTG GTCTGAGCTACTTGGGAGGCTGAGGCAGGAGTGTTGCTTGAGCCCAGGAGTTCAAGGCTACAGTG A G USP39 Ensembl:ENSG00000168883 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1441265349 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_310,RMVar_hsa_circ_334819,RMVar_hsa_circ_347953,RMVar_hsa_circ_332846,RMVar_hsa_circ_101891,RMVar_hsa_circ_201580,RMVar_hsa_circ_61594,RMVar_hsa_circ_305879,RMVar_hsa_circ_365253 44701 RMVar_ID_44701 Human_SNP_ID_80764058 A-to-I Human chr2 + 85643747 85643747 85643747 TCGGCTCACTGCAACCTTCGCCTCCTGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCGGAATAGG TCGGCTCACTGCAACCTTCGCCTCCTGGGTTCGAGCAATTCTCCTGCCTCAGCCTCCGGAATAGG A G USP39 Ensembl:ENSG00000168883 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1480750977 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_347953,RMVar_hsa_circ_101891,RMVar_hsa_circ_15778,RMVar_hsa_circ_201580,RMVar_hsa_circ_365253,RMVar_hsa_circ_201585,RMVar_hsa_circ_355012,RMVar_hsa_circ_314808,RMVar_hsa_circ_60504 44702 RMVar_ID_44702 Human_SNP_ID_80764068 A-to-I Human chr2 + 85643789 85643789 85643789 CCTGCCTCAGCCTCCGGAATAGGTGGGACTACAGGTGCACGCCGCCACGCCCAGCTAATTTTTTT CCTGCCTCAGCCTCCGGAATAGGTGGGACTACGGGTGCACGCCGCCACGCCCAGCTAATTTTTTT A G USP39 Ensembl:ENSG00000168883 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs983667362 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_347953,RMVar_hsa_circ_101891,RMVar_hsa_circ_15778,RMVar_hsa_circ_201580,RMVar_hsa_circ_365253,RMVar_hsa_circ_201585,RMVar_hsa_circ_355012,RMVar_hsa_circ_314808,RMVar_hsa_circ_60504 44703 RMVar_ID_44703 Human_SNP_ID_80855637 A-to-I Human chr2 - 86022681 86022681 86022681 AAGAGGCTGAGGTGAGAGGAGCAAGTGAGCCCAGGAGTTCAAGGCTGCAATGAGCTGTGATCGCA AAGAGGCTGAGGTGAGAGGAGCAAGTGAGCCCGGGAGTTCAAGGCTGCAATGAGCTGTGATCGCA T C POLR1A Ensembl:ENSG00000068654 Protein coding 3'UTR GSE100210;GSE107867 HepG2 cell line;ASD brains,temporal_cortex - 29129909,30559470 RNA-Seq:(High) rs1324175971 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_777848,Human_RBP_ID_13975059 Human_miRNA_ID_254550,Human_miRNA_ID_1158430 44704 RMVar_ID_44704 Human_SNP_ID_80855645 A-to-I Human chr2 - 86022713 86022711 86022713 GTTGTGACATGTGCCTGTGGTCCCAGCTACTCAAGAGGCTGAGGTGAGAGGAGCAAGTGAGCCCA GTTGTGACATGTGCCTGTGGTCCCAGCTACTC__GAGGCTGAGGTGAGAGGAGCAAGTGAGCCCA CTT C POLR1A Ensembl:ENSG00000068654 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1180924739 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_4618595,Human_RBP_ID_13975059 44705 RMVar_ID_44705 Human_SNP_ID_80855679 A-to-I Human chr2 - 86022869 86022869 86022869 GAAAAAAAAAAAGATTGATTCTGGCCGGGCACAGTGGCTCACGCTTACAGTCCCAGCACTTTAAG GAAAAAAAAAAAGATTGATTCTGGCCGGGCACGGTGGCTCACGCTTACAGTCCCAGCACTTTAAG T C POLR1A Ensembl:ENSG00000068654 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs565823388 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6954494,Human_RBP_ID_13975066 Human_miRNA_ID_1358686 44706 RMVar_ID_44706 Human_SNP_ID_80855716 A-to-I Human chr2 - 86023005 86023005 86023005 TTTAGTAGAGATGGGGTTTCACCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCGG TTTAGTAGAGATGGGGTTTCACCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCGG T C POLR1A Ensembl:ENSG00000068654 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1285545413 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6954496,Human_RBP_ID_13975075 44707 RMVar_ID_44707 Human_SNP_ID_80855979 A-to-I Human chr2 - 86023981 86023981 86023981 ACGTTGGGAGGCCGAGGCGGGCAGATCATCTGAGGTCAGGATTCGAGACCACCCTGGCCAACATG ACGTTGGGAGGCCGAGGCGGGCAGATCATCTGGGGTCAGGATTCGAGACCACCCTGGCCAACATG T C POLR1A Ensembl:ENSG00000068654 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1264204990 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18319669 44708 RMVar_ID_44708 Human_SNP_ID_80855982 A-to-I Human chr2 - 86023986 86023986 86023986 CCAATACGTTGGGAGGCCGAGGCGGGCAGATCATCTGAGGTCAGGATTCGAGACCACCCTGGCCA CCAATACGTTGGGAGGCCGAGGCGGGCAGATCGTCTGAGGTCAGGATTCGAGACCACCCTGGCCA T C POLR1A Ensembl:ENSG00000068654 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs897643536 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18319669 44709 RMVar_ID_44709 Human_SNP_ID_80855984 A-to-I Human chr2 - 86023991 86023991 86023991 TAATCCCAATACGTTGGGAGGCCGAGGCGGGCAGATCATCTGAGGTCAGGATTCGAGACCACCCT TAATCCCAATACGTTGGGAGGCCGAGGCGGGCGGATCATCTGAGGTCAGGATTCGAGACCACCCT T C POLR1A Ensembl:ENSG00000068654 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs747332210 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18319669 Human_miRNA_ID_461849,Human_miRNA_ID_928180 44710 RMVar_ID_44710 Human_SNP_ID_80855995 A-to-I Human chr2 - 86024028 86024028 86024028 TACAGATATCTGAGGCCAGGCCAGGCGTTCACACCTGTAATCCCAATACGTTGGGAGGCCGAGGC TACAGATATCTGAGGCCAGGCCAGGCGTTCACGCCTGTAATCCCAATACGTTGGGAGGCCGAGGC T C POLR1A Ensembl:ENSG00000068654 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1299871141 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1738785 44711 RMVar_ID_44711 Human_SNP_ID_80856209 A-to-I Human chr2 - 86024920 86024920 86024920 GTTGGCCAGGCTAGTCTCGAACTCCTAATCTCAGGTGATCCGCCTGCCTCAGCCTCCCAAAGTGC GTTGGCCAGGCTAGTCTCGAACTCCTAATCTCTGGTGATCCGCCTGCCTCAGCCTCCCAAAGTGC T A POLR1A Ensembl:ENSG00000068654 Protein coding 3'UTR GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs1257715897 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13975162 44712 RMVar_ID_44712 Human_SNP_ID_80856210 A-to-I Human chr2 - 86024926 86024926 86024926 CACCATGTTGGCCAGGCTAGTCTCGAACTCCTAATCTCAGGTGATCCGCCTGCCTCAGCCTCCCA CACCATGTTGGCCAGGCTAGTCTCGAACTCCTCATCTCAGGTGATCCGCCTGCCTCAGCCTCCCA T G POLR1A Ensembl:ENSG00000068654 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs184310590 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13975162 44713 RMVar_ID_44713 Human_SNP_ID_80856255 A-to-I Human chr2 - 86025074 86025074 86025074 GAGTGCAATGGCGCAATCTCGGCTCCACTGCAACCTCCATCTCCCGAGTTCAAGCGATTCTCCTG GAGTGCAATGGCGCAATCTCGGCTCCACTGCACCCTCCATCTCCCGAGTTCAAGCGATTCTCCTG T G POLR1A Ensembl:ENSG00000068654 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs901994952 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13975163 44714 RMVar_ID_44714 Human_SNP_ID_80856261 A-to-I Human chr2 - 86025091 86025091 86025091 CACTTGTTACCCAGGCTGAGTGCAATGGCGCAATCTCGGCTCCACTGCAACCTCCATCTCCCGAG CACTTGTTACCCAGGCTGAGTGCAATGGCGCAGTCTCGGCTCCACTGCAACCTCCATCTCCCGAG T C POLR1A Ensembl:ENSG00000068654 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1488998771 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13975163 44715 RMVar_ID_44715 Human_SNP_ID_80856264 A-to-I Human chr2 - 86025099 86025099 86025099 CACTTTTGCACTTGTTACCCAGGCTGAGTGCAATGGCGCAATCTCGGCTCCACTGCAACCTCCAT CACTTTTGCACTTGTTACCCAGGCTGAGTGCAGTGGCGCAATCTCGGCTCCACTGCAACCTCCAT T C POLR1A Ensembl:ENSG00000068654 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1380280336 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13975164 44716 RMVar_ID_44716 Human_SNP_ID_80866270 A-to-I Human chr2 - 86064208 86064208 86064208 GAAACCAGACTAACCCACAAACAAATTCTTGCATAGTGTAGTCACTCTTGCCCTTTTCACCTGTT GAAACCAGACTAACCCACAAACAAATTCTTGCGTAGTGTAGTCACTCTTGCCCTTTTCACCTGTT T C POLR1A Ensembl:ENSG00000068654 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1386040055 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 44717 RMVar_ID_44717 Human_SNP_ID_80871531 A-to-I Human chr2 - 86084357 86084357 86084357 GCTGGAGTGCAGCGATACGATCTCGGCTCCCTACAGCCTCTGCCTCTCAGGTTCAAGCGATTCTC GCTGGAGTGCAGCGATACGATCTCGGCTCCCTGCAGCCTCTGCCTCTCAGGTTCAAGCGATTCTC T C POLR1A Ensembl:ENSG00000068654 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs895751523 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13975855,Human_RBP_ID_25568696 RMVar_hsa_circ_104072,RMVar_hsa_circ_201610,RMVar_hsa_circ_116842,RMVar_hsa_circ_201616,RMVar_hsa_circ_90865,RMVar_hsa_circ_26914,RMVar_hsa_circ_201620,RMVar_hsa_circ_41764,RMVar_hsa_circ_201623,RMVar_hsa_circ_308838,RMVar_hsa_circ_95664,RMVar_hsa_circ_48160 44718 RMVar_ID_44718 Human_SNP_ID_80871544 A-to-I Human chr2 - 86084403 86084403 86084403 GTTTTGTGTTTTTTTTTTTGAGACAGGGTCTCACTTTGTCATCCAGGCTGGAGTGCAGCGATACG GTTTTGTGTTTTTTTTTTTGAGACAGGGTCTCTCTTTGTCATCCAGGCTGGAGTGCAGCGATACG T A POLR1A Ensembl:ENSG00000068654 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs576493926 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13975858,Human_RBP_ID_25568697 RMVar_hsa_circ_104072,RMVar_hsa_circ_201610,RMVar_hsa_circ_116842,RMVar_hsa_circ_201616,RMVar_hsa_circ_90865,RMVar_hsa_circ_26914,RMVar_hsa_circ_201620,RMVar_hsa_circ_41764,RMVar_hsa_circ_201623,RMVar_hsa_circ_308838,RMVar_hsa_circ_95664,RMVar_hsa_circ_48160 44719 RMVar_ID_44719 Human_SNP_ID_80871545 A-to-I Human chr2 - 86084403 86084403 86084403 GTTTTGTGTTTTTTTTTTTGAGACAGGGTCTCACTTTGTCATCCAGGCTGGAGTGCAGCGATACG GTTTTGTGTTTTTTTTTTTGAGACAGGGTCTCGCTTTGTCATCCAGGCTGGAGTGCAGCGATACG T C POLR1A Ensembl:ENSG00000068654 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs576493926 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13975858,Human_RBP_ID_25568697 RMVar_hsa_circ_104072,RMVar_hsa_circ_201610,RMVar_hsa_circ_116842,RMVar_hsa_circ_201616,RMVar_hsa_circ_90865,RMVar_hsa_circ_26914,RMVar_hsa_circ_201620,RMVar_hsa_circ_41764,RMVar_hsa_circ_201623,RMVar_hsa_circ_308838,RMVar_hsa_circ_95664,RMVar_hsa_circ_48160 44720 RMVar_ID_44720 Human_SNP_ID_80871548 A-to-I Human chr2 - 86084411 86084411 86084411 TTTGTTTTGTTTTGTGTTTTTTTTTTTGAGACAGGGTCTCACTTTGTCATCCAGGCTGGAGTGCA TTTGTTTTGTTTTGTGTTTTTTTTTTTGAGACGGGGTCTCACTTTGTCATCCAGGCTGGAGTGCA T C POLR1A Ensembl:ENSG00000068654 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1345536349 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104072,RMVar_hsa_circ_201610,RMVar_hsa_circ_116842,RMVar_hsa_circ_201616,RMVar_hsa_circ_90865,RMVar_hsa_circ_26914,RMVar_hsa_circ_201620,RMVar_hsa_circ_41764,RMVar_hsa_circ_201623,RMVar_hsa_circ_308838,RMVar_hsa_circ_95664,RMVar_hsa_circ_48160 44721 RMVar_ID_44721 Human_SNP_ID_80871691 A-to-I Human chr2 - 86084979 86084979 86084979 CCAGCCTGGTCGACAGAGCAAGTCTCTGTCTCAGAAAAAAAGAAAATACTGGACATGACTTAAAT CCAGCCTGGTCGACAGAGCAAGTCTCTGTCTCCGAAAAAAAGAAAATACTGGACATGACTTAAAT T G POLR1A Ensembl:ENSG00000068654 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs963780619 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13975872 RMVar_hsa_circ_104072,RMVar_hsa_circ_201610,RMVar_hsa_circ_116842,RMVar_hsa_circ_201616,RMVar_hsa_circ_90865,RMVar_hsa_circ_26914,RMVar_hsa_circ_201620,RMVar_hsa_circ_41764,RMVar_hsa_circ_201623,RMVar_hsa_circ_308838,RMVar_hsa_circ_95664,RMVar_hsa_circ_48160 44722 RMVar_ID_44722 Human_SNP_ID_80871696 A-to-I Human chr2 - 86084997 86084997 86084997 AGATCGTGCCACTGCACTCCAGCCTGGTCGACAGAGCAAGTCTCTGTCTCAGAAAAAAAGAAAAT AGATCGTGCCACTGCACTCCAGCCTGGTCGACGGAGCAAGTCTCTGTCTCAGAAAAAAAGAAAAT T C POLR1A Ensembl:ENSG00000068654 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1394225460 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104072,RMVar_hsa_circ_201610,RMVar_hsa_circ_116842,RMVar_hsa_circ_201616,RMVar_hsa_circ_90865,RMVar_hsa_circ_26914,RMVar_hsa_circ_201620,RMVar_hsa_circ_41764,RMVar_hsa_circ_201623,RMVar_hsa_circ_308838,RMVar_hsa_circ_95664,RMVar_hsa_circ_48160 44723 RMVar_ID_44723 Human_SNP_ID_80879299 A-to-I Human chr2 + 86114464 86114464 86114464 CGCCCCCACCCCCACGCCCGGCTAATTTTTGTATTTTTAGTAGAGACGGAGTTTCACTGTGTTAG CGCCCCCACCCCCACGCCCGGCTAATTTTTGTGTTTTTAGTAGAGACGGAGTTTCACTGTGTTAG A G PTCD3 Ensembl:ENSG00000132300 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1558794159 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22030,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_106553,RMVar_hsa_circ_201629,RMVar_hsa_circ_201630,RMVar_hsa_circ_201631,RMVar_hsa_circ_201628,RMVar_hsa_circ_348381,RMVar_hsa_circ_201633,RMVar_hsa_circ_89711,RMVar_hsa_circ_374567,RMVar_hsa_circ_201632,RMVar_hsa_circ_370249,RMVar_hsa_circ_101338,RMVar_hsa_circ_335511,RMVar_hsa_circ_90994,RMVar_hsa_circ_201634,RMVar_hsa_circ_201636,RMVar_hsa_circ_201637,RMVar_hsa_circ_201638,RMVar_hsa_circ_201635 44724 RMVar_ID_44724 Human_SNP_ID_80881309 A-to-I Human chr2 + 86122443 86122443 86122443 ATTTCTTGTTTCCCCCTCAGAGACAGGGTCTCACTCTGTCACCTAGGGTGGAGTGCAGTGATGCT ATTTCTTGTTTCCCCCTCAGAGACAGGGTCTCTCTCTGTCACCTAGGGTGGAGTGCAGTGATGCT A T PTCD3 Ensembl:ENSG00000132300 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1265252729 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125766,RMVar_hsa_circ_346100,RMVar_hsa_circ_71301,RMVar_hsa_circ_95968,RMVar_hsa_circ_64529,RMVar_hsa_circ_106553,RMVar_hsa_circ_201630,RMVar_hsa_circ_201631,RMVar_hsa_circ_201633,RMVar_hsa_circ_370249,RMVar_hsa_circ_101338,RMVar_hsa_circ_90994,RMVar_hsa_circ_77199,RMVar_hsa_circ_201644,RMVar_hsa_circ_92309,RMVar_hsa_circ_201634,RMVar_hsa_circ_201636,RMVar_hsa_circ_201635,RMVar_hsa_circ_96089,RMVar_hsa_circ_201641,RMVar_hsa_circ_201642,RMVar_hsa_circ_346989,RMVar_hsa_circ_79213,RMVar_hsa_circ_121328,RMVar_hsa_circ_291562,RMVar_hsa_circ_201645,RMVar_hsa_circ_369933,RMVar_hsa_circ_348699,RMVar_hsa_circ_362199,RMVar_hsa_circ_279144,RMVar_hsa_circ_290968,RMVar_hsa_circ_278682,RMVar_hsa_circ_104680,RMVar_hsa_circ_105971,RMVar_hsa_circ_101162,RMVar_hsa_circ_201647,RMVar_hsa_circ_201651,RMVar_hsa_circ_35222,RMVar_hsa_circ_76575,RMVar_hsa_circ_201652,RMVar_hsa_circ_201653,RMVar_hsa_circ_201649,RMVar_hsa_circ_201650,RMVar_hsa_circ_201648,RMVar_hsa_circ_201646 44725 RMVar_ID_44725 Human_SNP_ID_80885887 A-to-I Human chr2 + 86139666 86139666 86139666 CCTACAAAAGATTTTAATAATTAGTTGGGCGTAGTGGTGCATGCCTGTAATCCCAGCTACTCTGG CCTACAAAAGATTTTAATAATTAGTTGGGCGTGGTGGTGCATGCCTGTAATCCCAGCTACTCTGG A G PTCD3 Ensembl:ENSG00000132300 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs554085658 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6955011,Human_RBP_ID_8526525,Human_RBP_ID_13977486 RMVar_hsa_circ_121328,RMVar_hsa_circ_201646,RMVar_hsa_circ_85803,RMVar_hsa_circ_201669 44726 RMVar_ID_44726 Human_SNP_ID_80886677 A-to-I Human chr2 - 86142427 86142427 86142427 GTTTATTTATTATTATTATTCTTTTTTGAGACAGAGTCTCGCACTGTCGCCTGGGCTGGAGTGCA GTTTATTTATTATTATTATTCTTTTTTGAGACCGAGTCTCGCACTGTCGCCTGGGCTGGAGTGCA T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934236485 Functional Loss SNV dbSNP153 33..33 33 - - - 44727 RMVar_ID_44727 Human_SNP_ID_80890359 A-to-I Human chr2 - 86155136 86155136 86155136 AGGACTGGCCAGGTGCAGTGGCTTATGCCTATAATCCTAGCACTTTGGGAGGCTGAGGTGGGTGG AGGACTGGCCAGGTGCAGTGGCTTATGCCTATGATCCTAGCACTTTGGGAGGCTGAGGTGGGTGG T C IMMT Ensembl:ENSG00000132305 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1353810354 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87806,RMVar_hsa_circ_90910,RMVar_hsa_circ_201671,RMVar_hsa_circ_201672,RMVar_hsa_circ_201675,RMVar_hsa_circ_292476,RMVar_hsa_circ_28864,RMVar_hsa_circ_367216,RMVar_hsa_circ_320727,RMVar_hsa_circ_331550,RMVar_hsa_circ_346577,RMVar_hsa_circ_52358,RMVar_hsa_circ_284655,RMVar_hsa_circ_201676 44728 RMVar_ID_44728 Human_SNP_ID_80890360 A-to-I Human chr2 - 86155138 86155138 86155138 TCAGGACTGGCCAGGTGCAGTGGCTTATGCCTATAATCCTAGCACTTTGGGAGGCTGAGGTGGGT TCAGGACTGGCCAGGTGCAGTGGCTTATGCCTGTAATCCTAGCACTTTGGGAGGCTGAGGTGGGT T C IMMT Ensembl:ENSG00000132305 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs892027000 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25569218 RMVar_hsa_circ_87806,RMVar_hsa_circ_90910,RMVar_hsa_circ_201671,RMVar_hsa_circ_201672,RMVar_hsa_circ_201675,RMVar_hsa_circ_292476,RMVar_hsa_circ_28864,RMVar_hsa_circ_367216,RMVar_hsa_circ_320727,RMVar_hsa_circ_331550,RMVar_hsa_circ_346577,RMVar_hsa_circ_52358,RMVar_hsa_circ_284655,RMVar_hsa_circ_201676 44729 RMVar_ID_44729 Human_SNP_ID_80890907 A-to-I Human chr2 - 86157541 86157541 86157541 CCTCAAGTGATTCGCCCACCTTGGCCTCCCAAAATGCTGGGATTACAGGTGTGAGCCACCACACC CCTCAAGTGATTCGCCCACCTTGGCCTCCCAAGATGCTGGGATTACAGGTGTGAGCCACCACACC T C IMMT Ensembl:ENSG00000132305 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1454831775 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87806,RMVar_hsa_circ_90910,RMVar_hsa_circ_201671,RMVar_hsa_circ_201672,RMVar_hsa_circ_201675,RMVar_hsa_circ_292476,RMVar_hsa_circ_28864,RMVar_hsa_circ_367216,RMVar_hsa_circ_320727,RMVar_hsa_circ_331550,RMVar_hsa_circ_346577,RMVar_hsa_circ_52358,RMVar_hsa_circ_284655,RMVar_hsa_circ_201676 44730 RMVar_ID_44730 Human_SNP_ID_80890910 A-to-I Human chr2 - 86157556 86157556 86157556 GTTTTGAACTCCTGACCTCAAGTGATTCGCCCACCTTGGCCTCCCAAAATGCTGGGATTACAGGT GTTTTGAACTCCTGACCTCAAGTGATTCGCCCTCCTTGGCCTCCCAAAATGCTGGGATTACAGGT T A IMMT Ensembl:ENSG00000132305 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1022299750 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87806,RMVar_hsa_circ_90910,RMVar_hsa_circ_201671,RMVar_hsa_circ_201672,RMVar_hsa_circ_201675,RMVar_hsa_circ_292476,RMVar_hsa_circ_28864,RMVar_hsa_circ_367216,RMVar_hsa_circ_320727,RMVar_hsa_circ_331550,RMVar_hsa_circ_346577,RMVar_hsa_circ_52358,RMVar_hsa_circ_284655,RMVar_hsa_circ_201676 44731 RMVar_ID_44731 Human_SNP_ID_80890915 A-to-I Human chr2 - 86157568 86157568 86157568 TTGGCCAGGCTGGTTTTGAACTCCTGACCTCAAGTGATTCGCCCACCTTGGCCTCCCAAAATGCT TTGGCCAGGCTGGTTTTGAACTCCTGACCTCACGTGATTCGCCCACCTTGGCCTCCCAAAATGCT T G IMMT Ensembl:ENSG00000132305 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs985957350 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25569233 RMVar_hsa_circ_87806,RMVar_hsa_circ_90910,RMVar_hsa_circ_201671,RMVar_hsa_circ_201672,RMVar_hsa_circ_201675,RMVar_hsa_circ_292476,RMVar_hsa_circ_28864,RMVar_hsa_circ_367216,RMVar_hsa_circ_320727,RMVar_hsa_circ_331550,RMVar_hsa_circ_346577,RMVar_hsa_circ_52358,RMVar_hsa_circ_284655,RMVar_hsa_circ_201676 44732 RMVar_ID_44732 Human_SNP_ID_80890924 A-to-I Human chr2 - 86157603 86157603 86157603 TTTTGTACTTTTAGTAGAGACAGGGTTTCGCCATTTTGGCCAGGCTGGTTTTGAACTCCTGACCT TTTTGTACTTTTAGTAGAGACAGGGTTTCGCCGTTTTGGCCAGGCTGGTTTTGAACTCCTGACCT T C IMMT Ensembl:ENSG00000132305 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1319564964 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87806,RMVar_hsa_circ_90910,RMVar_hsa_circ_201671,RMVar_hsa_circ_201672,RMVar_hsa_circ_201675,RMVar_hsa_circ_292476,RMVar_hsa_circ_28864,RMVar_hsa_circ_367216,RMVar_hsa_circ_320727,RMVar_hsa_circ_331550,RMVar_hsa_circ_346577,RMVar_hsa_circ_52358,RMVar_hsa_circ_284655,RMVar_hsa_circ_201676 44733 RMVar_ID_44733 Human_SNP_ID_80892584 A-to-I Human chr2 - 86163788 86163788 86163788 CACCCATCTTAGTAGAGACAGGGTTTCACCATATTGGCCATGCTGGTCTTGAACTCCTGACCTCA CACCCATCTTAGTAGAGACAGGGTTTCACCATGTTGGCCATGCTGGTCTTGAACTCCTGACCTCA T C IMMT Ensembl:ENSG00000132305 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs911614680 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87806,RMVar_hsa_circ_201672,RMVar_hsa_circ_201675,RMVar_hsa_circ_292476,RMVar_hsa_circ_28864,RMVar_hsa_circ_331550,RMVar_hsa_circ_52358,RMVar_hsa_circ_284655,RMVar_hsa_circ_201676,RMVar_hsa_circ_119818,RMVar_hsa_circ_319222,RMVar_hsa_circ_201677,RMVar_hsa_circ_56513,RMVar_hsa_circ_303538,RMVar_hsa_circ_315563,RMVar_hsa_circ_314529,RMVar_hsa_circ_30117,RMVar_hsa_circ_201680,RMVar_hsa_circ_330407,RMVar_hsa_circ_320954,RMVar_hsa_circ_201681,RMVar_hsa_circ_296940 44734 RMVar_ID_44734 Human_SNP_ID_80892600 A-to-I Human chr2 - 86163864 86163864 86163864 ACCTCTGCTTCCCAGGTTCCAGCGATTCTCCTACCTCAGCCTCCAGAGTAGCTGGGATTACAGGC ACCTCTGCTTCCCAGGTTCCAGCGATTCTCCTGCCTCAGCCTCCAGAGTAGCTGGGATTACAGGC T C IMMT Ensembl:ENSG00000132305 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1419758268 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87806,RMVar_hsa_circ_201672,RMVar_hsa_circ_201675,RMVar_hsa_circ_292476,RMVar_hsa_circ_28864,RMVar_hsa_circ_331550,RMVar_hsa_circ_52358,RMVar_hsa_circ_284655,RMVar_hsa_circ_201676,RMVar_hsa_circ_119818,RMVar_hsa_circ_319222,RMVar_hsa_circ_201677,RMVar_hsa_circ_56513,RMVar_hsa_circ_303538,RMVar_hsa_circ_315563,RMVar_hsa_circ_314529,RMVar_hsa_circ_30117,RMVar_hsa_circ_201680,RMVar_hsa_circ_330407,RMVar_hsa_circ_320954,RMVar_hsa_circ_201681,RMVar_hsa_circ_296940 44735 RMVar_ID_44735 Human_SNP_ID_80892616 A-to-I Human chr2 - 86163918 86163918 86163918 GTCTTGCTTTGTTGCCCAGGCTGGAGTGCAATAGCGTGATCTCGGCTCACTGCAACCTCTGCTTC GTCTTGCTTTGTTGCCCAGGCTGGAGTGCAATGGCGTGATCTCGGCTCACTGCAACCTCTGCTTC T C IMMT Ensembl:ENSG00000132305 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1391522699 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87806,RMVar_hsa_circ_201672,RMVar_hsa_circ_201675,RMVar_hsa_circ_292476,RMVar_hsa_circ_28864,RMVar_hsa_circ_331550,RMVar_hsa_circ_52358,RMVar_hsa_circ_284655,RMVar_hsa_circ_201676,RMVar_hsa_circ_119818,RMVar_hsa_circ_319222,RMVar_hsa_circ_201677,RMVar_hsa_circ_56513,RMVar_hsa_circ_303538,RMVar_hsa_circ_315563,RMVar_hsa_circ_314529,RMVar_hsa_circ_30117,RMVar_hsa_circ_201680,RMVar_hsa_circ_330407,RMVar_hsa_circ_320954,RMVar_hsa_circ_201681,RMVar_hsa_circ_296940 44736 RMVar_ID_44736 Human_SNP_ID_80892762 A-to-I Human chr2 - 86164329 86164329 86164329 AAGCGGTCCAGGCGTGGTGGCTCATACCTGTAATCCCAGCACTGTGGGAGGCTGAGGCTGGTGGA AAGCGGTCCAGGCGTGGTGGCTCATACCTGTAGTCCCAGCACTGTGGGAGGCTGAGGCTGGTGGA T C IMMT Ensembl:ENSG00000132305 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1023705989 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87806,RMVar_hsa_circ_201672,RMVar_hsa_circ_201675,RMVar_hsa_circ_292476,RMVar_hsa_circ_28864,RMVar_hsa_circ_331550,RMVar_hsa_circ_52358,RMVar_hsa_circ_284655,RMVar_hsa_circ_201676,RMVar_hsa_circ_119818,RMVar_hsa_circ_319222,RMVar_hsa_circ_201677,RMVar_hsa_circ_56513,RMVar_hsa_circ_303538,RMVar_hsa_circ_315563,RMVar_hsa_circ_314529,RMVar_hsa_circ_30117,RMVar_hsa_circ_201680,RMVar_hsa_circ_330407,RMVar_hsa_circ_320954,RMVar_hsa_circ_201681,RMVar_hsa_circ_296940 44737 RMVar_ID_44737 Human_SNP_ID_80893818 A-to-I Human chr2 - 86168150 86168150 86168150 ACATTGGTGTCTGCTATTTCTTGAGTCCTTTTATGGAAGAACACTGTCCATTTCAAGTTGCCTTT ACATTGGTGTCTGCTATTTCTTGAGTCCTTTTGTGGAAGAACACTGTCCATTTCAAGTTGCCTTT T C IMMT Ensembl:ENSG00000132305 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1424516 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1099082 GWAS_ID_5069,GWAS_ID_5070,GWAS_ID_5071,GWAS_ID_5072,GWAS_ID_5073,GWAS_ID_5074,GWAS_ID_5075,GWAS_ID_5076,GWAS_ID_5077,GWAS_ID_5078,GWAS_ID_5079,GWAS_ID_5080,GWAS_ID_5081,GWAS_ID_5082,GWAS_ID_5083,GWAS_ID_5084,GWAS_ID_5085,GWAS_ID_5086,GWAS_ID_5087,GWAS_ID_5088,GWAS_ID_5089,GWAS_ID_5090,GWAS_ID_5091,GWAS_ID_5092,GWAS_ID_5093,GWAS_ID_5094,GWAS_ID_5095,GWAS_ID_5096,GWAS_ID_5097,GWAS_ID_5098,GWAS_ID_5099,GWAS_ID_5100,GWAS_ID_5101,GWAS_ID_5102,GWAS_ID_5103,GWAS_ID_5104,GWAS_ID_5105,GWAS_ID_5106,GWAS_ID_5107,GWAS_ID_5108,GWAS_ID_5109,GWAS_ID_5110,GWAS_ID_5111,GWAS_ID_5112 RMVar_hsa_circ_25525,RMVar_hsa_circ_28864,RMVar_hsa_circ_331550,RMVar_hsa_circ_52358,RMVar_hsa_circ_284655,RMVar_hsa_circ_201676,RMVar_hsa_circ_119818,RMVar_hsa_circ_319222,RMVar_hsa_circ_201677,RMVar_hsa_circ_56513,RMVar_hsa_circ_303538,RMVar_hsa_circ_314529,RMVar_hsa_circ_30117,RMVar_hsa_circ_201680,RMVar_hsa_circ_296940,RMVar_hsa_circ_289635,RMVar_hsa_circ_201682 44738 RMVar_ID_44738 Human_SNP_ID_80897346 A-to-I Human chr2 - 86182736 86182736 86182736 AGCTCAAGTGATTCTCATGCCTCAGCCTCCCAAGTATCTGGGACTATAGGCACATGCCACCAAAC AGCTCAAGTGATTCTCATGCCTCAGCCTCCCAGGTATCTGGGACTATAGGCACATGCCACCAAAC T C IMMT Ensembl:ENSG00000132305 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs977498500 Functional Loss SNV dbSNP153 33..33 33 - - - 44739 RMVar_ID_44739 Human_SNP_ID_80897366 A-to-I Human chr2 - 86182788 86182788 86182788 GGAGTGGAGTGACACAGTCTTGGCTCATTGCAACCTCCACCTCCGGGGCTCAAGCTCAAGTGATT GGAGTGGAGTGACACAGTCTTGGCTCATTGCAGCCTCCACCTCCGGGGCTCAAGCTCAAGTGATT T C IMMT Ensembl:ENSG00000132305 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1348478221 Functional Loss SNV dbSNP153 33..33 33 - - - 44740 RMVar_ID_44740 Human_SNP_ID_80903810 A-to-I Human chr2 + 86207784 86207784 86207784 ACACTTGAGGTCAGGCGTTGTGGCAGGTGCCTATAATCCCAGCTGCTTGGGAAGCTGAGGCAGGA ACACTTGAGGTCAGGCGTTGTGGCAGGTGCCTGTAATCCCAGCTGCTTGGGAAGCTGAGGCAGGA A G MRPL35 Ensembl:ENSG00000132313 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1451289128 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122945,RMVar_hsa_circ_201683,RMVar_hsa_circ_364110 44741 RMVar_ID_44741 Human_SNP_ID_80905951 A-to-I Human chr2 - 86217101 86217101 86217101 CACCTTTCTGTTTTCTCTACCAGGCACCGCCTAGAATCCTTCGATCTCGCTTCAGGAAGAAAAGT CACCTTTCTGTTTTCTCTACCAGGCACCGCCTGGAATCCTTCGATCTCGCTTCAGGAAGAAAAGT T C REEP1 Ensembl:ENSG00000068615 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs587781248 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_270950,Human_Splice_Rec_270962,Human_Splice_Rec_270966,Human_Splice_Rec_270982,Human_Splice_Rec_270994,Human_Splice_Rec_271008,Human_Splice_Rec_271018,Human_Splice_Rec_271026,Human_Splice_Rec_271038 Clinvar_Rec_127 RMVar_hsa_circ_201685 44742 RMVar_ID_44742 Human_SNP_ID_80965900 A-to-I Human chr2 + 86473651 86473651 86473651 ACATGCCTGCCTTCCCAGCCACTTGAGAGGCTAAGGTGGGAGGATTGCTGAAGTCTGGGAGTGGG ACATGCCTGCCTTCCCAGCCACTTGAGAGGCTGAGGTGGGAGGATTGCTGAAGTCTGGGAGTGGG A G KDM3A Ensembl:ENSG00000115548 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs986931746 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569791 RMVar_hsa_circ_5719,RMVar_hsa_circ_10475,RMVar_hsa_circ_12270,RMVar_hsa_circ_125429,RMVar_hsa_circ_201694,RMVar_hsa_circ_89502,RMVar_hsa_circ_83455,RMVar_hsa_circ_339241,RMVar_hsa_circ_201695,RMVar_hsa_circ_14972,RMVar_hsa_circ_201696,RMVar_hsa_circ_296003,RMVar_hsa_circ_345156,RMVar_hsa_circ_373399,RMVar_hsa_circ_121643,RMVar_hsa_circ_18794,RMVar_hsa_circ_201700,RMVar_hsa_circ_201701,RMVar_hsa_circ_201699 44743 RMVar_ID_44743 Human_SNP_ID_80987956 A-to-I Human chr2 - 86561570 86561570 86561570 TGTTTTTCCCCCCATTATGGACAAGTCTGGGTATTGTAGAGCAGTGCTTCTCAAGCATTAGTGTG TGTTTTTCCCCCCATTATGGACAAGTCTGGGTGTTGTAGAGCAGTGCTTCTCAAGCATTAGTGTG T C CHMP3,RNF103-CHMP3 Ensembl:ENSG00000115561,Ensembl:ENSG00000249884 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs939066879 Functional Loss SNV dbSNP153 33..33 33 - - - 44744 RMVar_ID_44744 Human_SNP_ID_80988130 A-to-I Human chr2 - 86562307 86562307 86562307 CATCAGTGCTTTGAGAAGCACTGCTCTGCAACACCTAGGCTTGTCCATAATGGAAAAAAAAAATC CATCAGTGCTTTGAGAAGCACTGCTCTGCAACTCCTAGGCTTGTCCATAATGGAAAAAAAAAATC T A CHMP3,RNF103-CHMP3 Ensembl:ENSG00000115561,Ensembl:ENSG00000249884 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223022172 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25569636 44745 RMVar_ID_44745 Human_SNP_ID_80988145 A-to-I Human chr2 - 86562353 86562352 86562353 GAGTCAGATTTTGAATTCTGACAAGCTCCCTAATGATTAGTGTGCACATCAGTGCTTTGAGAAGC GAGTCAGATTTTGAATTCTGACAAGCTCCCTA_TGATTAGTGTGCACATCAGTGCTTTGAGAAGC AT A CHMP3,RNF103-CHMP3 Ensembl:ENSG00000115561,Ensembl:ENSG00000249884 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1357237382 Functional Loss DEL dbSNP153 33..33 33 - - - 44746 RMVar_ID_44746 Human_SNP_ID_80988146 A-to-I Human chr2 - 86562353 86562353 86562353 GAGTCAGATTTTGAATTCTGACAAGCTCCCTAATGATTAGTGTGCACATCAGTGCTTTGAGAAGC GAGTCAGATTTTGAATTCTGACAAGCTCCCTAGTGATTAGTGTGCACATCAGTGCTTTGAGAAGC T C CHMP3,RNF103-CHMP3 Ensembl:ENSG00000115561,Ensembl:ENSG00000249884 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1045660474 Functional Loss SNV dbSNP153 33..33 33 - - - 44747 RMVar_ID_44747 Human_SNP_ID_81030541 A-to-I Human chr2 + 86755258 86755258 86755258 CTCCTGCCCCGGCCTCCTGAGTAGCTAAGACTACAGGTGCACACCACCACACCTGGCTAATTTTT CTCCTGCCCCGGCCTCCTGAGTAGCTAAGACTGCAGGTGCACACCACCACACCTGGCTAATTTTT A G RMND5A Ensembl:ENSG00000153561 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs992518416 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47773,RMVar_hsa_circ_321651,RMVar_hsa_circ_352683,RMVar_hsa_circ_76733,RMVar_hsa_circ_201708 44748 RMVar_ID_44748 Human_SNP_ID_81090668 A-to-I Human chr2 - 87050274 87050274 87050274 TTTGTTTGTTTGTTTGTTTGAGACAGAATCTCACTCTGTCACCCAGGCTGGAGTACAGTGGCACG TTTGTTTGTTTGTTTGTTTGAGACAGAATCTCGCTCTGTCACCCAGGCTGGAGTACAGTGGCACG T C AC125232.1,ANAPC1P2 Ensembl:ENSG00000285793,Ensembl:ENSG00000231259 lincRNA,Pseudogene intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs568039250 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10001313,Human_RBP_ID_17393226,Human_RBP_ID_17510388 RMVar_hsa_circ_201724,RMVar_hsa_circ_103919,RMVar_hsa_circ_201723,RMVar_hsa_circ_349991,RMVar_hsa_circ_201725,RMVar_hsa_circ_114907,RMVar_hsa_circ_309970 44749 RMVar_ID_44749 Human_SNP_ID_81090671 A-to-I Human chr2 - 87050279 87050279 87050279 TTTGTTTTGTTTGTTTGTTTGTTTGAGACAGAATCTCACTCTGTCACCCAGGCTGGAGTACAGTG TTTGTTTTGTTTGTTTGTTTGTTTGAGACAGAGTCTCACTCTGTCACCCAGGCTGGAGTACAGTG T C AC125232.1,ANAPC1P2 Ensembl:ENSG00000285793,Ensembl:ENSG00000231259 lincRNA,Pseudogene intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1287715643 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10001313,Human_RBP_ID_17393226,Human_RBP_ID_17510388 RMVar_hsa_circ_201724,RMVar_hsa_circ_103919,RMVar_hsa_circ_201723,RMVar_hsa_circ_349991,RMVar_hsa_circ_201725,RMVar_hsa_circ_114907,RMVar_hsa_circ_309970 44750 RMVar_ID_44750 Human_SNP_ID_81090821 A-to-I Human chr2 - 87050756 87050756 87050756 GGGAGGCTAAGGTTGAAAGATCGCTTGAGTCCAAGAGGTGGAGGTTGCAGGGAGCCATGATCACA GGGAGGCTAAGGTTGAAAGATCGCTTGAGTCCGAGAGGTGGAGGTTGCAGGGAGCCATGATCACA T C AC125232.1,ANAPC1P2 Ensembl:ENSG00000285793,Ensembl:ENSG00000231259 lincRNA,Pseudogene intron,intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs555400006 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_201724,RMVar_hsa_circ_103919,RMVar_hsa_circ_201723,RMVar_hsa_circ_349991,RMVar_hsa_circ_201725,RMVar_hsa_circ_114907,RMVar_hsa_circ_309970 44751 RMVar_ID_44751 Human_SNP_ID_81205820 A-to-I Human chr2 + 87461771 87461771 87461771 AGATATAGGCTGAAAGGTTAGCTAGGGATTCTAGAAAAGCTCTCTAAAGGAGACTGACATGTAAT AGATATAGGCTGAAAGGTTAGCTAGGGATTCTGGAAAAGCTCTCTAAAGGAGACTGACATGTAAT A G AC133644.2,CYTOR Ensembl:ENSG00000284879,Ensembl:ENSG00000222041 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1485020032 Functional Loss SNV dbSNP153 33..33 33 - - - 44752 RMVar_ID_44752 Human_SNP_ID_81210517 A-to-I Human chr2 + 87480866 87480866 87480866 GAGAGGATCGCTGAGCCTGGGAGGCAGAGGTTACAGTGAGCCAAGATGGCGCCGTTGTACTCCAA GAGAGGATCGCTGAGCCTGGGAGGCAGAGGTTGCAGTGAGCCAAGATGGCGCCGTTGTACTCCAA A G AC133644.2,CYTOR Ensembl:ENSG00000284879,Ensembl:ENSG00000222041 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1172991437 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23311211 44753 RMVar_ID_44753 Human_SNP_ID_81275672 A-to-I Human chr2 + 87762369 87762369 87762369 TGAGACCAGTTTTGCCAACATGGCGAAACCCCATCTCTGCTAAAAATACAAAAAATTAGCCAGGC TGAGACCAGTTTTGCCAACATGGCGAAACCCCGTCTCTGCTAAAAATACAAAAAATTAGCCAGGC A G AC133644.2 Ensembl:ENSG00000284879 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs984573255 Functional Loss SNV dbSNP153 33..33 33 - - - 44754 RMVar_ID_44754 Human_SNP_ID_81330541 A-to-I Human chr2 - 88029972 88029972 88029972 GTGGTGGTGTGCACCTGTAGTCTTAACTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCCT GTGGTGGTGTGCACCTGTAGTCTTAACTACTCCGGAGGCTGAGGCAGGAGAATCACTTGAACCCT T G KRCC1 Ensembl:ENSG00000172086 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs992419720 Functional Loss SNV dbSNP153 33..33 33 - - - 44755 RMVar_ID_44755 Human_SNP_ID_81330555 A-to-I Human chr2 - 88030030 88030030 88030030 CAGCCTGGCCAACATGGTGAAACCGCATCTCTACTAAAAATACAAAAATTAGCCAGGCGTGGTGG CAGCCTGGCCAACATGGTGAAACCGCATCTCTCCTAAAAATACAAAAATTAGCCAGGCGTGGTGG T G KRCC1 Ensembl:ENSG00000172086 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs941238718 Functional Loss SNV dbSNP153 33..33 33 - - - 44756 RMVar_ID_44756 Human_SNP_ID_81334170 A-to-I Human chr2 - 88046782 88046782 88046782 CCTGTAGTCCCAGCTACTGGGGAGGCTGAGGCAGGAGGATCAATTGAGCCTGGGAGGTTGAGGCT CCTGTAGTCCCAGCTACTGGGGAGGCTGAGGCGGGAGGATCAATTGAGCCTGGGAGGTTGAGGCT T C KRCC1 Ensembl:ENSG00000172086 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs568336375 Functional Loss SNV dbSNP153 33..33 33 - - - 44757 RMVar_ID_44757 Human_SNP_ID_81334171 A-to-I Human chr2 - 88046782 88046782 88046782 CCTGTAGTCCCAGCTACTGGGGAGGCTGAGGCAGGAGGATCAATTGAGCCTGGGAGGTTGAGGCT CCTGTAGTCCCAGCTACTGGGGAGGCTGAGGCCGGAGGATCAATTGAGCCTGGGAGGTTGAGGCT T G KRCC1 Ensembl:ENSG00000172086 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs568336375 Functional Loss SNV dbSNP153 33..33 33 - - - 44758 RMVar_ID_44758 Human_SNP_ID_81334880 A-to-I Human chr2 - 88049566 88049566 88049566 CAGCTCACTGCAGCCTCGACTTCCCCAGGCTCAGGTGATTCTCCCACCTCAGCCTCCTAAGTAGG CAGCTCACTGCAGCCTCGACTTCCCCAGGCTCGGGTGATTCTCCCACCTCAGCCTCCTAAGTAGG T C KRCC1 Ensembl:ENSG00000172086 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs996460437 Functional Loss SNV dbSNP153 33..33 33 - - - 44759 RMVar_ID_44759 Human_SNP_ID_81335098 A-to-I Human chr2 - 88050449 88050449 88050449 CCAGCTAATTTTTGTGTTTTATTAGTAGAGACAGGATTTCACCGTGTTGGCTGGGCTGGTTTTGG CCAGCTAATTTTTGTGTTTTATTAGTAGAGACGGGATTTCACCGTGTTGGCTGGGCTGGTTTTGG T C KRCC1 Ensembl:ENSG00000172086 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs993929222 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6956242,Human_RBP_ID_17569793 44760 RMVar_ID_44760 Human_SNP_ID_81335279 A-to-I Human chr2 - 88051002 88051002 88051002 GGAGGACTGCTTGAATCCAGGAGGTCGAGGCTACGGTGAGCTGTGATCACACCACTACACTTCAG GGAGGACTGCTTGAATCCAGGAGGTCGAGGCTGCGGTGAGCTGTGATCACACCACTACACTTCAG T C KRCC1 Ensembl:ENSG00000172086 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1343082900 Functional Loss SNV dbSNP153 33..33 33 - - - 44761 RMVar_ID_44761 Human_SNP_ID_81464554 A-to-I Human chr2 - 88561158 88561158 88561158 CTTGAGGCCAGAGTTCAACACCAGCCTGGGCAACATAGTAAGACCCCATCTCTACAAAAAATTTA CTTGAGGCCAGAGTTCAACACCAGCCTGGGCAGCATAGTAAGACCCCATCTCTACAAAAAATTTA T C EIF2AK3 Ensembl:ENSG00000172071 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1363635780 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_201737,RMVar_hsa_circ_94785,RMVar_hsa_circ_269708 44762 RMVar_ID_44762 Human_SNP_ID_81465873 A-to-I Human chr2 - 88566938 88566938 88566938 GCTGGCTGGAAATTTTATTATTTTTTTGAGACAGGGTCTTTGTCACTCAGGCTGGAGTATAGTCA GCTGGCTGGAAATTTTATTATTTTTTTGAGACCGGGTCTTTGTCACTCAGGCTGGAGTATAGTCA T G EIF2AK3 Ensembl:ENSG00000172071 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs778180672 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8526815 RMVar_hsa_circ_63451,RMVar_hsa_circ_201737,RMVar_hsa_circ_94785,RMVar_hsa_circ_269708 44763 RMVar_ID_44763 Human_SNP_ID_81754470 A-to-I Human chr2 + 89807883 89807883 89807883 ATCATCGAATGCAACCGAATGGAATCATCATCAAATGGAAACGAAAGGAGTCATCATCGAATGGA ATCATCGAATGCAACCGAATGGAATCATCATCGAATGGAAACGAAAGGAGTCATCATCGAATGGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs796958700 Functional Loss SNV dbSNP153 33..33 33 - - - 44764 RMVar_ID_44764 Human_SNP_ID_48266987 A-to-I Human chr1 + 210569215 210569215 210569215 GGCCAACATGGCGAAACCCCATCTCTACTAAAAATACAAAAATTAGCCGGGTGCAGTGGCGGGCA GGCCAACATGGCGAAACCCCATCTCTACTAAAGATACAAAAATTAGCCGGGTGCAGTGGCGGGCA A G HHAT Ensembl:ENSG00000054392 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs542401038 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6784,RMVar_hsa_circ_139367,RMVar_hsa_circ_89588,RMVar_hsa_circ_338440,RMVar_hsa_circ_139370 44765 RMVar_ID_44765 Human_SNP_ID_48266988 A-to-I Human chr1 + 210569218 210569218 210569218 CAACATGGCGAAACCCCATCTCTACTAAAAATACAAAAATTAGCCGGGTGCAGTGGCGGGCACCT CAACATGGCGAAACCCCATCTCTACTAAAAATGCAAAAATTAGCCGGGTGCAGTGGCGGGCACCT A G HHAT Ensembl:ENSG00000054392 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1326415998 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6784,RMVar_hsa_circ_139367,RMVar_hsa_circ_89588,RMVar_hsa_circ_338440,RMVar_hsa_circ_139370 44766 RMVar_ID_44766 Human_SNP_ID_48276009 A-to-I Human chr1 + 210604758 210604758 210604758 AAATTGAAAGTTGGATGTAGTGGCTCATACCTATAATCCCAACACTTTGAGGGGCCAAGGTGGGA AAATTGAAAGTTGGATGTAGTGGCTCATACCTGTAATCCCAACACTTTGAGGGGCCAAGGTGGGA A G HHAT Ensembl:ENSG00000054392 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1211533018 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139367,RMVar_hsa_circ_89588,RMVar_hsa_circ_338440,RMVar_hsa_circ_139370 44767 RMVar_ID_44767 Human_SNP_ID_48338662 A-to-I Human chr1 - 210867700 210867700 210867700 AAAACTTACTTAAAATGACATAAAGTAGATCAATTGTTGCCTAGGGTTGGGCATTTTGAGACAGA AAAACTTACTTAAAATGACATAAAGTAGATCAGTTGTTGCCTAGGGTTGGGCATTTTGAGACAGA T C AL590132.1,KCNH1 Ensembl:ENSG00000284299,Ensembl:ENSG00000143473 Protein coding,Protein coding intron,intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs561044763 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82775,RMVar_hsa_circ_107793,RMVar_hsa_circ_139372,RMVar_hsa_circ_77283,RMVar_hsa_circ_139373,RMVar_hsa_circ_139374 44768 RMVar_ID_44768 Human_SNP_ID_48435100 A-to-I Human chr1 + 211262295 211262295 211262295 CCTGACCTCGTGATCTGCTGCCTCGACCTCCCAAAGTGTTGGGATTACAGGTATGAGCCATCGCG CCTGACCTCGTGATCTGCTGCCTCGACCTCCCGAAGTGTTGGGATTACAGGTATGAGCCATCGCG A G RCOR3 Ensembl:ENSG00000117625 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1449919462 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22708033 RMVar_hsa_circ_43365,RMVar_hsa_circ_356794,RMVar_hsa_circ_368956,RMVar_hsa_circ_304306,RMVar_hsa_circ_346715,RMVar_hsa_circ_46735 44769 RMVar_ID_44769 Human_SNP_ID_48435566 A-to-I Human chr1 + 211263920 211263920 211263920 TTGGCTCACTGCAACCTCCACCTCCTGGGTTCAAGCAATTCTGCCTCAGCCTCCCAAGTAGCTGG TTGGCTCACTGCAACCTCCACCTCCTGGGTTCGAGCAATTCTGCCTCAGCCTCCCAAGTAGCTGG A G RCOR3 Ensembl:ENSG00000117625 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1243934974 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43365,RMVar_hsa_circ_356794,RMVar_hsa_circ_368956,RMVar_hsa_circ_304306,RMVar_hsa_circ_346715,RMVar_hsa_circ_46735 44770 RMVar_ID_44770 Human_SNP_ID_48435592 A-to-I Human chr1 + 211264006 211264006 211264006 TACCCGGCTAATTTTGTTTTTTGTATTTTTGTAGAGAAAAGGTTTCACCATGTTGGCCGGGCTAG TACCCGGCTAATTTTGTTTTTTGTATTTTTGTGGAGAAAAGGTTTCACCATGTTGGCCGGGCTAG A G RCOR3 Ensembl:ENSG00000117625 Protein coding intron GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs1558039473 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10750211,Human_RBP_ID_17557416 RMVar_hsa_circ_43365,RMVar_hsa_circ_356794,RMVar_hsa_circ_368956,RMVar_hsa_circ_304306,RMVar_hsa_circ_346715,RMVar_hsa_circ_46735 44771 RMVar_ID_44771 Human_SNP_ID_48435594 A-to-I Human chr1 + 211264012 211264012 211264012 GCTAATTTTGTTTTTTGTATTTTTGTAGAGAAAAGGTTTCACCATGTTGGCCGGGCTAGTCTTGA GCTAATTTTGTTTTTTGTATTTTTGTAGAGAAGAGGTTTCACCATGTTGGCCGGGCTAGTCTTGA A G RCOR3 Ensembl:ENSG00000117625 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1343261163 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17557416 RMVar_hsa_circ_43365,RMVar_hsa_circ_356794,RMVar_hsa_circ_368956,RMVar_hsa_circ_304306,RMVar_hsa_circ_346715,RMVar_hsa_circ_46735 44772 RMVar_ID_44772 Human_SNP_ID_48435695 A-to-I Human chr1 + 211264424 211264424 211264424 AATGAATTGGCCAGGGGTCATAGCTCATGAGTATAATCCCAGCTCTTTGGGAGGCTGAGGTGAGA AATGAATTGGCCAGGGGTCATAGCTCATGAGTGTAATCCCAGCTCTTTGGGAGGCTGAGGTGAGA A G RCOR3 Ensembl:ENSG00000117625 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs964731206 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43365,RMVar_hsa_circ_356794,RMVar_hsa_circ_368956,RMVar_hsa_circ_304306,RMVar_hsa_circ_346715,RMVar_hsa_circ_46735 44773 RMVar_ID_44773 Human_SNP_ID_48435709 A-to-I Human chr1 + 211264498 211264498 211264498 GAGCCCAGGAGTTTGAGACCAGCCTGGGCAACATAGTGGGACCCTGTCTCCACAAAAAATTCAAA GAGCCCAGGAGTTTGAGACCAGCCTGGGCAACGTAGTGGGACCCTGTCTCCACAAAAAATTCAAA A G RCOR3 Ensembl:ENSG00000117625 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1047624577 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43365,RMVar_hsa_circ_356794,RMVar_hsa_circ_368956,RMVar_hsa_circ_304306,RMVar_hsa_circ_346715,RMVar_hsa_circ_46735 44774 RMVar_ID_44774 Human_SNP_ID_48435734 A-to-I Human chr1 + 211264628 211264628 211264628 ATCACTTGAGTCCAGGAAGTTGAGGCTGCAGTAAGCTATGATGGCGCCACTGTACTATACCCTGG ATCACTTGAGTCCAGGAAGTTGAGGCTGCAGTGAGCTATGATGGCGCCACTGTACTATACCCTGG A G RCOR3 Ensembl:ENSG00000117625 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs999756444 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43365,RMVar_hsa_circ_356794,RMVar_hsa_circ_368956,RMVar_hsa_circ_304306,RMVar_hsa_circ_346715,RMVar_hsa_circ_46735 44775 RMVar_ID_44775 Human_SNP_ID_48436010 A-to-I Human chr1 + 211265598 211265598 211265598 AAAATCAGCTGGGCGTGGTAGTGGGCACCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGA AAAATCAGCTGGGCGTGGTAGTGGGCACCTGTCATCCCAGCTACTTGGGAGGCTGAGGCAGGAGA A C RCOR3 Ensembl:ENSG00000117625 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs781437215 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43365,RMVar_hsa_circ_356794,RMVar_hsa_circ_368956,RMVar_hsa_circ_304306,RMVar_hsa_circ_346715,RMVar_hsa_circ_46735 44776 RMVar_ID_44776 Human_SNP_ID_48436525 A-to-I Human chr1 + 211267757 211267757 211267757 GGGACTACAGGTGCACACGATCACATCCAGCTAATTTTTTGTGTTTTTAGTAGAGACAAGGTCTT GGGACTACAGGTGCACACGATCACATCCAGCTGATTTTTTGTGTTTTTAGTAGAGACAAGGTCTT A G RCOR3 Ensembl:ENSG00000117625 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs948540526 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43365,RMVar_hsa_circ_356794,RMVar_hsa_circ_368956,RMVar_hsa_circ_304306,RMVar_hsa_circ_346715,RMVar_hsa_circ_46735 44777 RMVar_ID_44777 Human_SNP_ID_48439185 A-to-I Human chr1 + 211278224 211278214 211278224 ATGGATCGCCAGGCTCGTAAACTAGCTAATAGACATAATCAGGGTGACAGGTAGGTTGGTTACCT ATGGATCGCCAGGCTCGTAAACT__________CATAATCAGGGTGACAGGTAGGTTGGTTACCT TAGCTAATAGA T RCOR3 Ensembl:ENSG00000117625 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1387864438 Functional Loss DEL dbSNP153 24..33 33 - - - Human_RBP_ID_855775 Human_Splice_Rec_184825,Human_Splice_Rec_184845,Human_Splice_Rec_184867,Human_Splice_Rec_184889,Human_Splice_Rec_184919,Human_Splice_Rec_184929 RMVar_hsa_circ_43365,RMVar_hsa_circ_356794,RMVar_hsa_circ_368956,RMVar_hsa_circ_304306,RMVar_hsa_circ_346715,RMVar_hsa_circ_36183,RMVar_hsa_circ_354289,RMVar_hsa_circ_377609,RMVar_hsa_circ_305804,RMVar_hsa_circ_315606,RMVar_hsa_circ_283153,RMVar_hsa_circ_139387,RMVar_hsa_circ_139389,RMVar_hsa_circ_139388,RMVar_hsa_circ_68355,RMVar_hsa_circ_71063,RMVar_hsa_circ_362987,RMVar_hsa_circ_35922,RMVar_hsa_circ_310111,RMVar_hsa_circ_69664,RMVar_hsa_circ_139391 44778 RMVar_ID_44778 Human_SNP_ID_48445785 A-to-I Human chr1 + 211307350 211307350 211307350 TCTTCACTGAAAATACAAAAAATTAGCCAGGTATGGTGGTGCACACGTGTAGTCCCAGCTGCTTG TCTTCACTGAAAATACAAAAAATTAGCCAGGTGTGGTGGTGCACACGTGTAGTCCCAGCTGCTTG A G RCOR3 Ensembl:ENSG00000117625 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1484697733 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_68355,RMVar_hsa_circ_71063,RMVar_hsa_circ_64390,RMVar_hsa_circ_47454 44779 RMVar_ID_44779 Human_SNP_ID_48466509 A-to-I Human chr1 + 211398144 211398144 211398144 GCAATTCTCCTGCCACAGCCTCCTAAGTAGCTAGGACTACACGCATGCACCACCACACCTGGCTA GCAATTCTCCTGCCACAGCCTCCTAAGTAGCTGGGACTACACGCATGCACCACCACACCTGGCTA A G LINC00467 Ensembl:ENSG00000153363 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1014043189 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126246,RMVar_hsa_circ_139400 44780 RMVar_ID_44780 Human_SNP_ID_48471524 A-to-I Human chr1 + 211417639 211417639 211417639 TTGAAGCAACTAAGGTCTGTTGAAGGAACGGTAGAGAAGAGTGGTAGAAGATGTGTGCTGGTCGT TTGAAGCAACTAAGGTCTGTTGAAGGAACGGTGGAGAAGAGTGGTAGAAGATGTGTGCTGGTCGT A G LINC00467,SNX25P1 Ensembl:ENSG00000153363,Ensembl:ENSG00000236809 lincRNA,Pseudogene intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1321100800 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126246,RMVar_hsa_circ_139400 44781 RMVar_ID_44781 Human_SNP_ID_48475094 A-to-I Human chr1 + 211433322 211433322 211433322 CACCATGTTGGCCAGGCTGGTCTCGAACTCCTAACCTCAGGTGATCTACCCACTTCAGTCTCCCA CACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCTACCCACTTCAGTCTCCCA A G LINC00467 Ensembl:ENSG00000153363 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1443567982 Functional Loss SNV dbSNP153 33..33 33 - - - 44782 RMVar_ID_44782 Human_SNP_ID_48475197 A-to-I Human chr1 + 211433752 211433752 211433752 GTGGTGACTGAGGCTTGTAATCCCAGCACTTTAGGAGGCCAAGGCAGGCGGATTGCTTTAGCTCA GTGGTGACTGAGGCTTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGCGGATTGCTTTAGCTCA A G LINC00467 Ensembl:ENSG00000153363 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1021774334 Functional Loss SNV dbSNP153 33..33 33 - - - 44783 RMVar_ID_44783 Human_SNP_ID_48475303 A-to-I Human chr1 + 211433934 211433934 211433934 AAATTTAGCCAGGCATGGTGGCACATGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGTGGGAGG AAATTTAGCCAGGCATGGTGGCACATGCCTGTGGTCCCAGCTACTCGGGAGGCTGAGGTGGGAGG A G LINC00467 Ensembl:ENSG00000153363 lincRNA exon GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1244834431 Functional Loss SNV dbSNP153 33..33 33 - - - 44784 RMVar_ID_44784 Human_SNP_ID_48475317 A-to-I Human chr1 + 211433987 211433987 211433987 TGAGGTGGGAGGATTGCTTGAGCTTGGGAGGCAGAGGCTGCGGTGAGCGAAGATCACACCACTGC TGAGGTGGGAGGATTGCTTGAGCTTGGGAGGCGGAGGCTGCGGTGAGCGAAGATCACACCACTGC A G LINC00467 Ensembl:ENSG00000153363 lincRNA exon GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs929135041 Functional Loss SNV dbSNP153 33..33 33 - - - 44785 RMVar_ID_44785 Human_SNP_ID_48475336 A-to-I Human chr1 + 211434042 211434042 211434042 ACACCACTGCACTCCAGCCTGGGCGCCAGAGCAAGACTCTGTCTACAAAAAACAACAAACAGAAA ACACCACTGCACTCCAGCCTGGGCGCCAGAGCGAGACTCTGTCTACAAAAAACAACAAACAGAAA A G LINC00467 Ensembl:ENSG00000153363 lincRNA exon GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs952542951 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_185345 44786 RMVar_ID_44786 Human_SNP_ID_48475490 A-to-I Human chr1 + 211434697 211434697 211434697 ATTTAATATGCTGTTCGTAGGCCAGGCTCAGTAGCTCACGCCTGTAATCTCAGCACTTTGGGACG ATTTAATATGCTGTTCGTAGGCCAGGCTCAGTGGCTCACGCCTGTAATCTCAGCACTTTGGGACG A G LINC00467 Ensembl:ENSG00000153363 lincRNA exon GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs906057455 Functional Loss SNV dbSNP153 33..33 33 - - - 44787 RMVar_ID_44787 Human_SNP_ID_48475511 A-to-I Human chr1 + 211434772 211434772 211434772 GAGGATCTCTTGAGCCCCCAGGAGTTTGAGACAAGCCTGGGCAGCATAAAGAGACCCCCATCTCT GAGGATCTCTTGAGCCCCCAGGAGTTTGAGACGAGCCTGGGCAGCATAAAGAGACCCCCATCTCT A G LINC00467 Ensembl:ENSG00000153363 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1478177792 Functional Loss SNV dbSNP153 33..33 33 - - - 44788 RMVar_ID_44788 Human_SNP_ID_48475515 A-to-I Human chr1 + 211434787 211434787 211434787 CCCCAGGAGTTTGAGACAAGCCTGGGCAGCATAAAGAGACCCCCATCTCTAAAAAAAAAAAAATA CCCCAGGAGTTTGAGACAAGCCTGGGCAGCATGAAGAGACCCCCATCTCTAAAAAAAAAAAAATA A G LINC00467 Ensembl:ENSG00000153363 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs944882269 Functional Loss SNV dbSNP153 33..33 33 - - - 44789 RMVar_ID_44789 Human_SNP_ID_48475537 A-to-I Human chr1 + 211434854 211434854 211434854 AAAATTAGCCAGACATGATGATGCCAACCTGTAGTCCTGGCTACTTGGGAAGCTGAGGTAGGAGG AAAATTAGCCAGACATGATGATGCCAACCTGTGGTCCTGGCTACTTGGGAAGCTGAGGTAGGAGG A G LINC00467 Ensembl:ENSG00000153363 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1302216787 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26375152 44790 RMVar_ID_44790 Human_SNP_ID_48475544 A-to-I Human chr1 + 211434881 211434881 211434881 CCTGTAGTCCTGGCTACTTGGGAAGCTGAGGTAGGAGGATCGCTTGAGCCCAGGAATTTGAGGCT CCTGTAGTCCTGGCTACTTGGGAAGCTGAGGTGGGAGGATCGCTTGAGCCCAGGAATTTGAGGCT A G LINC00467 Ensembl:ENSG00000153363 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285687905 Functional Loss SNV dbSNP153 33..33 33 - - - 44791 RMVar_ID_44791 Human_SNP_ID_48526820 A-to-I Human chr1 + 211640997 211640997 211640997 AAAATTAGCTTGGCGTGGTGGCGCGTGCCTGTAGTCCTAGCTACTCGGAAGGCTGAGCCAGGAGA AAAATTAGCTTGGCGTGGTGGCGCGTGCCTGTCGTCCTAGCTACTCGGAAGGCTGAGCCAGGAGA A C LINC01693 Ensembl:ENSG00000227764 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1466115998 Functional Loss SNV dbSNP153 33..33 33 - - - 44792 RMVar_ID_44792 Human_SNP_ID_48527869 A-to-I Human chr1 + 211645176 211645176 211645176 ACAATTAGCCCAGCATAGTGGCATGTGCCTGTAGTCCCAGCTACTTGAGAGGCTGAGGTGGGAGG ACAATTAGCCCAGCATAGTGGCATGTGCCTGTCGTCCCAGCTACTTGAGAGGCTGAGGTGGGAGG A C LINC01693 Ensembl:ENSG00000227764 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1228122260 Functional Loss SNV dbSNP153 33..33 33 - - - 44793 RMVar_ID_44793 Human_SNP_ID_48531653 A-to-I Human chr1 + 211660783 211660783 211660783 TCAGTCTGATAGGAACTCTGCAGGAAGAGCTCAATCAGGTTCAGGTAATAGGGCTGCTCCCAACA TCAGTCTGATAGGAACTCTGCAGGAAGAGCTCCATCAGGTTCAGGTAATAGGGCTGCTCCCAACA A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1261201448 Functional Loss SNV dbSNP153 33..33 33 - - - 44794 RMVar_ID_44794 Human_SNP_ID_48561739 A-to-I Human chr1 - 211791585 211791585 211791585 GGGTACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCGCCATGTTGGCCAGGC GGGTACCATGCCTGGCTAATTTTTGTATTTTTGGTAGAGACGGGGTTTCGCCATGTTGGCCAGGC T C LPGAT1 Ensembl:ENSG00000123684 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1436449237 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139410,RMVar_hsa_circ_139405,RMVar_hsa_circ_330485,RMVar_hsa_circ_335137,RMVar_hsa_circ_272874,RMVar_hsa_circ_139408,RMVar_hsa_circ_139409,RMVar_hsa_circ_139412,RMVar_hsa_circ_271587,RMVar_hsa_circ_70454,RMVar_hsa_circ_139411,RMVar_hsa_circ_277659 44795 RMVar_ID_44795 Human_SNP_ID_48562093 A-to-I Human chr1 - 211792900 211792900 211792900 CGAGGCCATCCAGGACAACAGGGTGAAACCCCATCTCTACTAAAAATACAGAAATTAGCTGGGCG CGAGGCCATCCAGGACAACAGGGTGAAACCCCGTCTCTACTAAAAATACAGAAATTAGCTGGGCG T C LPGAT1 Ensembl:ENSG00000123684 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1346310899 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139410,RMVar_hsa_circ_139405,RMVar_hsa_circ_330485,RMVar_hsa_circ_335137,RMVar_hsa_circ_272874,RMVar_hsa_circ_139408,RMVar_hsa_circ_139409,RMVar_hsa_circ_139412,RMVar_hsa_circ_271587,RMVar_hsa_circ_70454,RMVar_hsa_circ_139411,RMVar_hsa_circ_277659 44796 RMVar_ID_44796 Human_SNP_ID_48562492 A-to-I Human chr1 - 211794572 211794572 211794572 GCCGAGTGCAGTGGCTCATGTCTGTAATGTCAATACTTTGAGAGGCTGAAGCCGGTGGATTGCTT GCCGAGTGCAGTGGCTCATGTCTGTAATGTCAGTACTTTGAGAGGCTGAAGCCGGTGGATTGCTT T C LPGAT1 Ensembl:ENSG00000123684 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006832745 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139410,RMVar_hsa_circ_330485,RMVar_hsa_circ_70454 44797 RMVar_ID_44797 Human_SNP_ID_48564004 A-to-I Human chr1 - 211801545 211801545 211801545 CCCAGTTAAGTTCTTTTAAAAATTTTTTTTGTAGAGATGAGGTCTTGCTTTGTCGCCCATGCTGA CCCAGTTAAGTTCTTTTAAAAATTTTTTTTGTGGAGATGAGGTCTTGCTTTGTCGCCCATGCTGA T C LPGAT1 Ensembl:ENSG00000123684 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs368627530 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10751822 RMVar_hsa_circ_139410,RMVar_hsa_circ_330485,RMVar_hsa_circ_70454 44798 RMVar_ID_44798 Human_SNP_ID_48564134 A-to-I Human chr1 - 211802074 211802074 211802074 TCTCTTTTTTTTTTTTTTTGAGACAGAGTCTCACTCTGTTACCCAGGCTGTAATACAGTGGTGCA TCTCTTTTTTTTTTTTTTTGAGACAGAGTCTCTCTCTGTTACCCAGGCTGTAATACAGTGGTGCA T A LPGAT1 Ensembl:ENSG00000123684 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404175245 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139410,RMVar_hsa_circ_330485,RMVar_hsa_circ_70454 44799 RMVar_ID_44799 Human_SNP_ID_48567511 A-to-I Human chr1 - 211817389 211817389 211817389 TTTTGTATTTTCAGTAGAGACGAGGTTTTGCCATGTTGGCCAGGCTGGTCTCGAACTCCGGACCT TTTTGTATTTTCAGTAGAGACGAGGTTTTGCCGTGTTGGCCAGGCTGGTCTCGAACTCCGGACCT T C LPGAT1 Ensembl:ENSG00000123684 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1242718412 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139410,RMVar_hsa_circ_330485,RMVar_hsa_circ_70454 44800 RMVar_ID_44800 Human_SNP_ID_48567512 A-to-I Human chr1 - 211817389 211817389 211817389 TTTTGTATTTTCAGTAGAGACGAGGTTTTGCCATGTTGGCCAGGCTGGTCTCGAACTCCGGACCT TTTTGTATTTTCAGTAGAGACGAGGTTTTGCCCTGTTGGCCAGGCTGGTCTCGAACTCCGGACCT T G LPGAT1 Ensembl:ENSG00000123684 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1242718412 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139410,RMVar_hsa_circ_330485,RMVar_hsa_circ_70454 44801 RMVar_ID_44801 Human_SNP_ID_48568401 A-to-I Human chr1 - 211821242 211821238 211821242 ATACGTTTTTTGTTTTTTTGAGATGGAGTCTCACTCTGTTTCCCAGGCTGGAGTGCAGTGGTGCG ATACGTTTTTTGTTTTTTTGAGATGGAGTCTC____TGTTTCCCAGGCTGGAGTGCAGTGGTGCG AGAGT A LPGAT1 Ensembl:ENSG00000123684 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1243820853 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_139410,RMVar_hsa_circ_330485,RMVar_hsa_circ_70454 44802 RMVar_ID_44802 Human_SNP_ID_48604059 A-to-I Human chr1 - 211969659 211969659 211969659 CCCGGCTACTTGGGAAACTCAGGTGGGGGGATAATTTGAGCCCAGGAAGTTGAGGCTGCAGTGAG CCCGGCTACTTGGGAAACTCAGGTGGGGGGATTATTTGAGCCCAGGAAGTTGAGGCTGCAGTGAG T A INTS7 Ensembl:ENSG00000143493 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1347831482 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10753118 RMVar_hsa_circ_14223,RMVar_hsa_circ_103246,RMVar_hsa_circ_139414,RMVar_hsa_circ_121830,RMVar_hsa_circ_69988,RMVar_hsa_circ_139416,RMVar_hsa_circ_325813,RMVar_hsa_circ_284011,RMVar_hsa_circ_48501,RMVar_hsa_circ_139419,RMVar_hsa_circ_372723 44803 RMVar_ID_44803 Human_SNP_ID_48604513 A-to-I Human chr1 - 211971833 211971833 211971833 TGGCTCACTGCAACCTCCACCTCCCAGGTTCAAGTGATTCTCCTGCCTCACCCTTCCAAGTAGCT TGGCTCACTGCAACCTCCACCTCCCAGGTTCAGGTGATTCTCCTGCCTCACCCTTCCAAGTAGCT T C INTS7 Ensembl:ENSG00000143493 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1031789586 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14223,RMVar_hsa_circ_103246,RMVar_hsa_circ_139414,RMVar_hsa_circ_121830,RMVar_hsa_circ_69988,RMVar_hsa_circ_139416,RMVar_hsa_circ_325813,RMVar_hsa_circ_284011,RMVar_hsa_circ_48501,RMVar_hsa_circ_139419,RMVar_hsa_circ_372723 44804 RMVar_ID_44804 Human_SNP_ID_48614270 A-to-I Human chr1 - 212014273 212014273 212014273 TTTAGTAAAGATGGGGTTTCAGCACGTTGGCCAGGCTCGTCTTGAACTCCTGACCTCAGGTGATC TTTAGTAAAGATGGGGTTTCAGCACGTTGGCCGGGCTCGTCTTGAACTCCTGACCTCAGGTGATC T C INTS7 Ensembl:ENSG00000143493 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1337464729 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139423,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_139426,RMVar_hsa_circ_20687,RMVar_hsa_circ_354209,RMVar_hsa_circ_331665,RMVar_hsa_circ_314151,RMVar_hsa_circ_139428,RMVar_hsa_circ_276427,RMVar_hsa_circ_139427,RMVar_hsa_circ_70193 44805 RMVar_ID_44805 Human_SNP_ID_48622828 A-to-I Human chr1 + 212048942 212048942 212048942 GTTTGTTTGTTTGTTTGTTTGTTTGTTTTTTGAGACAAAGTCTCACTCTGTTGCCCAGGCTGGAA GTTTGTTTGTTTGTTTGTTTGTTTGTTTTTTGCGACAAAGTCTCACTCTGTTGCCCAGGCTGGAA A C DTL Ensembl:ENSG00000143476 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1236655421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5749632 RMVar_hsa_circ_1003,RMVar_hsa_circ_106846,RMVar_hsa_circ_139431,RMVar_hsa_circ_347045,RMVar_hsa_circ_7205,RMVar_hsa_circ_81612,RMVar_hsa_circ_351124,RMVar_hsa_circ_110421,RMVar_hsa_circ_139436,RMVar_hsa_circ_139437,RMVar_hsa_circ_139435,RMVar_hsa_circ_23790,RMVar_hsa_circ_95311,RMVar_hsa_circ_139439 44806 RMVar_ID_44806 Human_SNP_ID_48691986 A-to-I Human chr1 + 212338577 212338577 212338577 GTGGATCATGAGGTCAGAAGGATCATGAGGTCAGGAGTTCGAGACCAGCCTGAACAACATGGTGA GTGGATCATGAGGTCAGAAGGATCATGAGGTCCGGAGTTCGAGACCAGCCTGAACAACATGGTGA A C PPP2R5A Ensembl:ENSG00000066027 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs561947521 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2120270 RMVar_hsa_circ_139451,RMVar_hsa_circ_302751,RMVar_hsa_circ_363027,RMVar_hsa_circ_365584,RMVar_hsa_circ_329665,RMVar_hsa_circ_336681,RMVar_hsa_circ_313199,RMVar_hsa_circ_282903,RMVar_hsa_circ_290689,RMVar_hsa_circ_139453,RMVar_hsa_circ_139454,RMVar_hsa_circ_139452,RMVar_hsa_circ_139457,RMVar_hsa_circ_299723,RMVar_hsa_circ_340957,RMVar_hsa_circ_356924,RMVar_hsa_circ_315620,RMVar_hsa_circ_43967,RMVar_hsa_circ_139456 44807 RMVar_ID_44807 Human_SNP_ID_48691999 A-to-I Human chr1 + 212338625 212338625 212338625 CCTGAACAACATGGTGAAACCCCGTCTCTACTAAGAATACAAAAATTAGCCAGGCATGGTGGCAC CCTGAACAACATGGTGAAACCCCGTCTCTACTGAGAATACAAAAATTAGCCAGGCATGGTGGCAC A G PPP2R5A Ensembl:ENSG00000066027 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs988690174 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139451,RMVar_hsa_circ_302751,RMVar_hsa_circ_363027,RMVar_hsa_circ_365584,RMVar_hsa_circ_329665,RMVar_hsa_circ_336681,RMVar_hsa_circ_313199,RMVar_hsa_circ_282903,RMVar_hsa_circ_290689,RMVar_hsa_circ_139453,RMVar_hsa_circ_139454,RMVar_hsa_circ_139452,RMVar_hsa_circ_139457,RMVar_hsa_circ_299723,RMVar_hsa_circ_340957,RMVar_hsa_circ_356924,RMVar_hsa_circ_315620,RMVar_hsa_circ_43967,RMVar_hsa_circ_139456 44808 RMVar_ID_44808 Human_SNP_ID_48695180 A-to-I Human chr1 + 212352297 212352297 212352297 GCAGTGTGCCTTCCTTGGCCTTCCAAAGTGCTAGGATTACAGTTGTAAGCCACTGCACCTGGCCC GCAGTGTGCCTTCCTTGGCCTTCCAAAGTGCTGGGATTACAGTTGTAAGCCACTGCACCTGGCCC A G PPP2R5A Ensembl:ENSG00000066027 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1201008996 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139451,RMVar_hsa_circ_363027,RMVar_hsa_circ_336681,RMVar_hsa_circ_290689,RMVar_hsa_circ_43967,RMVar_hsa_circ_345981,RMVar_hsa_circ_139461,RMVar_hsa_circ_112716,RMVar_hsa_circ_139463,RMVar_hsa_circ_63025 44809 RMVar_ID_44809 Human_SNP_ID_48757324 A-to-I Human chr1 + 212615759 212615759 212615759 CCAGGAGGTTGAGGCTGCAATGAGCCGTGATCACCTCACTGCACTCCAGCCTGGGTGATGGAGCA CCAGGAGGTTGAGGCTGCAATGAGCCGTGATCGCCTCACTGCACTCCAGCCTGGGTGATGGAGCA A G ATF3 Ensembl:ENSG00000162772 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs372572909 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49934,RMVar_hsa_circ_362277 44810 RMVar_ID_44810 Human_SNP_ID_48790159 A-to-I Human chr1 - 212756222 212756222 212756222 CCAGCTACTCGGGAAGCTGCAGAGGGAGGATCATTTGAACCCAGGAGGTCAAGGCTGCAGTGAGC CCAGCTACTCGGGAAGCTGCAGAGGGAGGATCGTTTGAACCCAGGAGGTCAAGGCTGCAGTGAGC T C NSL1 Ensembl:ENSG00000117697 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1354876168 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3992,RMVar_hsa_circ_343811,RMVar_hsa_circ_343931,RMVar_hsa_circ_139468 44811 RMVar_ID_44811 Human_SNP_ID_48804697 A-to-I Human chr1 + 212811917 212811917 212811917 TAGAGATGGGGTTTCACCATGTTGGCCAGGCTAGTCTTGAACTCCTGACCTTATGTTCTGTCTGC TAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGACCTTATGTTCTGTCTGC A G TATDN3 Ensembl:ENSG00000203705 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350920972 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_65570,RMVar_hsa_circ_332214,RMVar_hsa_circ_333800,RMVar_hsa_circ_139478,RMVar_hsa_circ_350040 44812 RMVar_ID_44812 Human_SNP_ID_48819239 A-to-I Human chr1 + 212870910 212870910 212870910 CCTCAGCCTCCTAAGTAGCTGTAACTACAGGCATGTGCCACCATTAATGCCTGGCTAATTTTTGT CCTCAGCCTCCTAAGTAGCTGTAACTACAGGCGTGTGCCACCATTAATGCCTGGCTAATTTTTGT A G FLVCR1 Ensembl:ENSG00000162769 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs993902551 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_274806,RMVar_hsa_circ_279318,RMVar_hsa_circ_369325,RMVar_hsa_circ_279100,RMVar_hsa_circ_274626,RMVar_hsa_circ_139483,RMVar_hsa_circ_139485,RMVar_hsa_circ_139487,RMVar_hsa_circ_139488,RMVar_hsa_circ_139486,RMVar_hsa_circ_139484,RMVar_hsa_circ_139489,RMVar_hsa_circ_139490 44813 RMVar_ID_44813 Human_SNP_ID_48822982 A-to-I Human chr1 + 212885625 212885625 212885625 CAGGCTAGAGTGCAGTGGCGCAATCTCGGCTCACTGCAACCTCTGTCTCCCGGCTTCACGCCATT CAGGCTAGAGTGCAGTGGCGCAATCTCGGCTCGCTGCAACCTCTGTCTCCCGGCTTCACGCCATT A G FLVCR1 Ensembl:ENSG00000162769 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1320163432 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103574,RMVar_hsa_circ_274806,RMVar_hsa_circ_279100,RMVar_hsa_circ_139487,RMVar_hsa_circ_139488,RMVar_hsa_circ_139486,RMVar_hsa_circ_139490,RMVar_hsa_circ_268358,RMVar_hsa_circ_285510,RMVar_hsa_circ_367728,RMVar_hsa_circ_125264,RMVar_hsa_circ_139491,RMVar_hsa_circ_139493,RMVar_hsa_circ_139495,RMVar_hsa_circ_139494,RMVar_hsa_circ_139492,RMVar_hsa_circ_350273,RMVar_hsa_circ_365136,RMVar_hsa_circ_265318 44814 RMVar_ID_44814 Human_SNP_ID_48823168 A-to-I Human chr1 + 212886226 212886226 212886226 ACCACACCCGGCTAATTTTTTGACTTTTTGATAGAGACAGTGTTTCACCATGTTGCCCAGGCTGA ACCACACCCGGCTAATTTTTTGACTTTTTGATGGAGACAGTGTTTCACCATGTTGCCCAGGCTGA A G FLVCR1 Ensembl:ENSG00000162769 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1360977407 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10761926 RMVar_hsa_circ_103574,RMVar_hsa_circ_274806,RMVar_hsa_circ_279100,RMVar_hsa_circ_139487,RMVar_hsa_circ_139488,RMVar_hsa_circ_139486,RMVar_hsa_circ_139490,RMVar_hsa_circ_268358,RMVar_hsa_circ_285510,RMVar_hsa_circ_367728,RMVar_hsa_circ_125264,RMVar_hsa_circ_139491,RMVar_hsa_circ_139493,RMVar_hsa_circ_139495,RMVar_hsa_circ_139494,RMVar_hsa_circ_139492,RMVar_hsa_circ_350273,RMVar_hsa_circ_365136,RMVar_hsa_circ_265318 44815 RMVar_ID_44815 Human_SNP_ID_48823177 A-to-I Human chr1 + 212886290 212886290 212886290 ATTTTGAACTCCTGAGGTCAGGCAATCTGCCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGC ATTTTGAACTCCTGAGGTCAGGCAATCTGCCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGC A G FLVCR1 Ensembl:ENSG00000162769 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1044520238 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103574,RMVar_hsa_circ_274806,RMVar_hsa_circ_279100,RMVar_hsa_circ_139487,RMVar_hsa_circ_139488,RMVar_hsa_circ_139486,RMVar_hsa_circ_139490,RMVar_hsa_circ_268358,RMVar_hsa_circ_285510,RMVar_hsa_circ_367728,RMVar_hsa_circ_125264,RMVar_hsa_circ_139491,RMVar_hsa_circ_139493,RMVar_hsa_circ_139495,RMVar_hsa_circ_139494,RMVar_hsa_circ_139492,RMVar_hsa_circ_350273,RMVar_hsa_circ_365136,RMVar_hsa_circ_265318 44816 RMVar_ID_44816 Human_SNP_ID_48823282 A-to-I Human chr1 + 212886725 212886725 212886725 AGGAGGCTAAGGAAGGAGAATTGCTTGAACCCAGGAGGCAGAGGTTGCAGCGAGCTGAGATAGCG AGGAGGCTAAGGAAGGAGAATTGCTTGAACCCGGGAGGCAGAGGTTGCAGCGAGCTGAGATAGCG A G FLVCR1 Ensembl:ENSG00000162769 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs897262838 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103574,RMVar_hsa_circ_274806,RMVar_hsa_circ_279100,RMVar_hsa_circ_139487,RMVar_hsa_circ_139488,RMVar_hsa_circ_139486,RMVar_hsa_circ_139490,RMVar_hsa_circ_268358,RMVar_hsa_circ_285510,RMVar_hsa_circ_367728,RMVar_hsa_circ_125264,RMVar_hsa_circ_139491,RMVar_hsa_circ_139493,RMVar_hsa_circ_139495,RMVar_hsa_circ_139494,RMVar_hsa_circ_139492,RMVar_hsa_circ_350273,RMVar_hsa_circ_365136,RMVar_hsa_circ_265318 44817 RMVar_ID_44817 Human_SNP_ID_48843666 A-to-I Human chr1 + 212966797 212966797 212966797 AAATGTCTTTGAAAATTCAGTGATATGATCTCAGCTCGCTGCAACTTCCGCCTCCCAGGCTCAAG AAATGTCTTTGAAAATTCAGTGATATGATCTCCGCTCGCTGCAACTTCCGCCTCCCAGGCTCAAG A C VASH2 Ensembl:ENSG00000143494 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs923147453 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84574,RMVar_hsa_circ_139501,RMVar_hsa_circ_298162,RMVar_hsa_circ_139503 44818 RMVar_ID_44818 Human_SNP_ID_48843705 A-to-I Human chr1 + 212967006 212967006 212967006 AGCTCAAGTGATCCGCCCACCTCAGCCTCCCAAAGTGTTGAGATTAGAGGCAGGAGCCATCGCGC AGCTCAAGTGATCCGCCCACCTCAGCCTCCCAGAGTGTTGAGATTAGAGGCAGGAGCCATCGCGC A G VASH2 Ensembl:ENSG00000143494 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1002647115 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_186535 RMVar_hsa_circ_84574,RMVar_hsa_circ_139501,RMVar_hsa_circ_298162,RMVar_hsa_circ_139503 44819 RMVar_ID_44819 Human_SNP_ID_48850183 A-to-I Human chr1 - 212994242 212994242 212994242 GTTTCACTCTTGTTGCCCAGGCTGGGGGTGCAATGGCGCAATCTTTGCTCACTGCAACCCCTGCC GTTTCACTCTTGTTGCCCAGGCTGGGGGTGCAGTGGCGCAATCTTTGCTCACTGCAACCCCTGCC T C ANGEL2 Ensembl:ENSG00000174606 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1433373685 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5751790,Human_RBP_ID_10762339,Human_RBP_ID_17738052 44820 RMVar_ID_44820 Human_SNP_ID_48853899 A-to-I Human chr1 - 213008254 213008254 213008254 ATTGCCGGCGGCCAGTATTACACTGGAGTTTTAGGTTTCCCAATATTCTGAAAGAAATTAAACAT ATTGCCGGCGGCCAGTATTACACTGGAGTTTTCGGTTTCCCAATATTCTGAAAGAAATTAAACAT T G ANGEL2 Ensembl:ENSG00000174606 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1479865520 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1735319,Human_RBP_ID_8742562,Human_RBP_ID_27175091,Human_RBP_ID_27393719 Human_Splice_Rec_186541,Human_Splice_Rec_186557,Human_Splice_Rec_186571,Human_Splice_Rec_186593,Human_Splice_Rec_186599 RMVar_hsa_circ_302708,RMVar_hsa_circ_315270,RMVar_hsa_circ_139506,RMVar_hsa_circ_376465,RMVar_hsa_circ_269787 44821 RMVar_ID_44821 Human_SNP_ID_49159662 A-to-I Human chr1 + 214299732 214299732 214299732 GAGTTCAAGTAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGAGACTACAGGCGCCCGCCACCACG GAGTTCAAGTAATTCTCCTGCCTCAGCCTCCCCAGTAGCTGAGACTACAGGCGCCCGCCACCACG A C SMYD2 Ensembl:ENSG00000143499 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1487345033 Functional Loss SNV dbSNP153 33..33 33 - - - 44822 RMVar_ID_44822 Human_SNP_ID_49171575 A-to-I Human chr1 - 214350689 214350689 214350689 AAAAAAAAAAAAAATTAGCCAGGCATGGTGGCACATGCCTGTAATCCCAGCTACTCAGGAGGCTG AAAAAAAAAAAAAATTAGCCAGGCATGGTGGCGCATGCCTGTAATCCCAGCTACTCAGGAGGCTG T C AL929236.1,PTPN14 Ensembl:ENSG00000228470,Ensembl:ENSG00000152104 lincRNA,Protein coding intron,3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1177785194 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_95276 Human_miRNA_ID_1355089 RMVar_hsa_circ_139556,RMVar_hsa_circ_115192 44823 RMVar_ID_44823 Human_SNP_ID_49171579 A-to-I Human chr1 - 214350701 214350701 214350701 TACAAAAAAAAAAAAAAAAAAAAAAATTAGCCAGGCATGGTGGCACATGCCTGTAATCCCAGCTA TACAAAAAAAAAAAAAAAAAAAAAAATTAGCCGGGCATGGTGGCACATGCCTGTAATCCCAGCTA T C AL929236.1,PTPN14 Ensembl:ENSG00000228470,Ensembl:ENSG00000152104 lincRNA,Protein coding intron,3'UTR GSE47997;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,31158229,31158229 RNA-Seq:(High) rs1461577719 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_95276 RMVar_hsa_circ_139556,RMVar_hsa_circ_115192 44824 RMVar_ID_44824 Human_SNP_ID_49171624 A-to-I Human chr1 - 214350724 214350724 214350724 TGAAATCCCGTCTCTACTAAAAATACAAAAAAAAAAAAAAAAAAAAAAATTAGCCAGGCATGGTG TGAAATCCCGTCTCTACTAAAAATACAAAAAATAAAAAAAAAAAAAAAATTAGCCAGGCATGGTG T A AL929236.1,PTPN14 Ensembl:ENSG00000228470,Ensembl:ENSG00000152104 lincRNA,Protein coding intron,3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1165478516 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139556,RMVar_hsa_circ_115192 44825 RMVar_ID_44825 Human_SNP_ID_49171642 A-to-I Human chr1 - 214350762 214350762 214350762 CTGAGGTCAGGCGTTCAAGACCAGCCTGGCCAACATGGTGAAATCCCGTCTCTACTAAAAATACA CTGAGGTCAGGCGTTCAAGACCAGCCTGGCCATCATGGTGAAATCCCGTCTCTACTAAAAATACA T A AL929236.1,PTPN14 Ensembl:ENSG00000228470,Ensembl:ENSG00000152104 lincRNA,Protein coding intron,3'UTR GSE100210;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229 RNA-Seq:(High) rs1328541250 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139556,RMVar_hsa_circ_115192 44826 RMVar_ID_44826 Human_SNP_ID_49171644 A-to-I Human chr1 - 214350777 214350777 214350777 AGGCAGGCAGATCACCTGAGGTCAGGCGTTCAAGACCAGCCTGGCCAACATGGTGAAATCCCGTC AGGCAGGCAGATCACCTGAGGTCAGGCGTTCAGGACCAGCCTGGCCAACATGGTGAAATCCCGTC T C AL929236.1,PTPN14 Ensembl:ENSG00000228470,Ensembl:ENSG00000152104 lincRNA,Protein coding intron,3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,31158229,32596459 RNA-Seq:(High) rs1399787166 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139556,RMVar_hsa_circ_115192 44827 RMVar_ID_44827 Human_SNP_ID_49171706 A-to-I Human chr1 - 214351091 214351091 214351091 GACCCCCCTCGGCCTCCCAAAGTGCTGGGATTACACCCAGCCTCTGCTGCCTTTTCATATTTCCC GACCCCCCTCGGCCTCCCAAAGTGCTGGGATTGCACCCAGCCTCTGCTGCCTTTTCATATTTCCC T C AL929236.1,PTPN14 Ensembl:ENSG00000228470,Ensembl:ENSG00000152104 lincRNA,Protein coding intron,3'UTR GSE38233;GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;ASD brains,frontal_cortex;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,30559470,31158229,32596459 RNA-Seq:(High) rs1176266843 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2271196,Human_miRNA_ID_2712410,Human_miRNA_ID_3048393 RMVar_hsa_circ_139556,RMVar_hsa_circ_115192 44828 RMVar_ID_44828 Human_SNP_ID_49171722 A-to-I Human chr1 - 214351153 214351153 214351153 TTTAGTAGAGACGGGGTTTTGCCATGTTGGCCAGACTGGTCTCAAACCTCTGACCTCGTGATGAC TTTAGTAGAGACGGGGTTTTGCCATGTTGGCCGGACTGGTCTCAAACCTCTGACCTCGTGATGAC T C AL929236.1,PTPN14 Ensembl:ENSG00000228470,Ensembl:ENSG00000152104 lincRNA,Protein coding intron,3'UTR GSE100210;GSE99789;GSE107867 HepG2 cell line;esophageal squamous carcinoma cells,EC109;ASD brains,frontal_cortex - 29129909,29796672,30559470 RNA-Seq:(High) rs1357255885 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139556,RMVar_hsa_circ_115192 44829 RMVar_ID_44829 Human_SNP_ID_49171725 A-to-I Human chr1 - 214351162 214351162 214351162 TTTTATATTTTTAGTAGAGACGGGGTTTTGCCATGTTGGCCAGACTGGTCTCAAACCTCTGACCT TTTTATATTTTTAGTAGAGACGGGGTTTTGCCGTGTTGGCCAGACTGGTCTCAAACCTCTGACCT T C AL929236.1,PTPN14 Ensembl:ENSG00000228470,Ensembl:ENSG00000152104 lincRNA,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1320184387 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139556,RMVar_hsa_circ_115192 44830 RMVar_ID_44830 Human_SNP_ID_49171732 A-to-I Human chr1 - 214351179 214351179 214351179 CACCACACCCGGCTAATTTTTATATTTTTAGTAGAGACGGGGTTTTGCCATGTTGGCCAGACTGG CACCACACCCGGCTAATTTTTATATTTTTAGTGGAGACGGGGTTTTGCCATGTTGGCCAGACTGG T C AL929236.1,PTPN14 Ensembl:ENSG00000228470,Ensembl:ENSG00000152104 lincRNA,Protein coding intron,3'UTR GSE47997;GSE99789;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;esophageal squamous carcinoma cells,EC109;ASD brains,Fragile X samples from NIH NeuroBioBank;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,29796672,30559470,31158229,31158229,31158229 RNA-Seq:(High) rs1180988577 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139556,RMVar_hsa_circ_115192 44831 RMVar_ID_44831 Human_SNP_ID_49171734 A-to-I Human chr1 - 214351182 214351182 214351182 CACCACCACACCCGGCTAATTTTTATATTTTTAGTAGAGACGGGGTTTTGCCATGTTGGCCAGAC CACCACCACACCCGGCTAATTTTTATATTTTTGGTAGAGACGGGGTTTTGCCATGTTGGCCAGAC T C AL929236.1,PTPN14 Ensembl:ENSG00000228470,Ensembl:ENSG00000152104 lincRNA,Protein coding intron,3'UTR GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs1472654473 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139556,RMVar_hsa_circ_115192 44832 RMVar_ID_44832 Human_SNP_ID_49171736 A-to-I Human chr1 - 214351190 214351190 214351190 TAGGCGTGCACCACCACACCCGGCTAATTTTTATATTTTTAGTAGAGACGGGGTTTTGCCATGTT TAGGCGTGCACCACCACACCCGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTTGCCATGTT T C AL929236.1,PTPN14 Ensembl:ENSG00000228470,Ensembl:ENSG00000152104 lincRNA,Protein coding intron,3'UTR GSE47997;GSE99789;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829 K562 cells&HepG2 cells;esophageal squamous carcinoma cells,EC109;ASD brains,Fragile X samples from NIH NeuroBioBank;Bronchiolar epithelium,BEP2D cell line - 23474544,29796672,30559470,31158229 RNA-Seq:(High) rs1195807148 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139556,RMVar_hsa_circ_115192 44833 RMVar_ID_44833 Human_SNP_ID_49171744 A-to-I Human chr1 - 214351213 214351213 214351213 AGCCTCCAAAGTAGCTGGGATTATAGGCGTGCACCACCACACCCGGCTAATTTTTATATTTTTAG AGCCTCCAAAGTAGCTGGGATTATAGGCGTGCGCCACCACACCCGGCTAATTTTTATATTTTTAG T C AL929236.1,PTPN14 Ensembl:ENSG00000228470,Ensembl:ENSG00000152104 lincRNA,Protein coding intron,3'UTR GSE47997;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 23474544,29129909,29796672,31158229,31158229 RNA-Seq:(High) rs1377276766 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139556,RMVar_hsa_circ_115192 44834 RMVar_ID_44834 Human_SNP_ID_49171752 A-to-I Human chr1 - 214351223 214351223 214351223 GCTGGAGTGCAGCCTCCAAAGTAGCTGGGATTATAGGCGTGCACCACCACACCCGGCTAATTTTT GCTGGAGTGCAGCCTCCAAAGTAGCTGGGATTGTAGGCGTGCACCACCACACCCGGCTAATTTTT T C AL929236.1,PTPN14 Ensembl:ENSG00000228470,Ensembl:ENSG00000152104 lincRNA,Protein coding intron,3'UTR GSE47997;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,29129909,29796672,31158229,31158229,31158229 RNA-Seq:(High) rs1406237275 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139556,RMVar_hsa_circ_115192 44835 RMVar_ID_44835 Human_SNP_ID_49171756 A-to-I Human chr1 - 214351233 214351233 214351233 TGTTGCGCAGGCTGGAGTGCAGCCTCCAAAGTAGCTGGGATTATAGGCGTGCACCACCACACCCG TGTTGCGCAGGCTGGAGTGCAGCCTCCAAAGTGGCTGGGATTATAGGCGTGCACCACCACACCCG T C AL929236.1,PTPN14 Ensembl:ENSG00000228470,Ensembl:ENSG00000152104 lincRNA,Protein coding intron,3'UTR GSE47997;GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829 K562 cells&HepG2 cells;HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank;Bronchiolar epithelium,BEP2D cell line - 23474544,29129909,30559470,31158229 RNA-Seq:(High) rs1403191934 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139556,RMVar_hsa_circ_115192 44836 RMVar_ID_44836 Human_SNP_ID_49172728 A-to-I Human chr1 - 214355827 214355822 214355828 TTCTTCATTGCTGCTTTTGTCCCCCGTGAGCTAAAAAGATGGAGTGACATCAAATCAACCAGAAA TTCTTCATTGCTGCTTTTGTCCCCCGTGAGC______GATGGAGTGACATCAAATCAACCAGAAA CTTTTTA C AL929236.1,PTPN14 Ensembl:ENSG00000228470,Ensembl:ENSG00000152104 lincRNA,Protein coding intron,3'UTR GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459,32596459 RNA-Seq:(High) rs1353778864 Functional Loss DEL dbSNP153 32..37 33 - - - Human_RBP_ID_5245724,Human_RBP_ID_17449620 RMVar_hsa_circ_139556,RMVar_hsa_circ_115192 44837 RMVar_ID_44837 Human_SNP_ID_49172729 A-to-I Human chr1 - 214355827 214355827 214355827 TTCTTCATTGCTGCTTTTGTCCCCCGTGAGCTAAAAAGATGGAGTGACATCAAATCAACCAGAAA TTCTTCATTGCTGCTTTTGTCCCCCGTGAGCTGAAAAGATGGAGTGACATCAAATCAACCAGAAA T C AL929236.1,PTPN14 Ensembl:ENSG00000228470,Ensembl:ENSG00000152104 lincRNA,Protein coding intron,3'UTR GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459,32596459 RNA-Seq:(High) rs1037481193 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5245724,Human_RBP_ID_17449620 RMVar_hsa_circ_139556,RMVar_hsa_circ_115192 44838 RMVar_ID_44838 Human_SNP_ID_49172872 A-to-I Human chr1 - 214356348 214356348 214356348 TTAATTTGATGCCACATCTTCCTTGTCTTTTCAGCTTGGGAAAAAGGCGGCAGTGGAGGAAGGCA TTAATTTGATGCCACATCTTCCTTGTCTTTTCGGCTTGGGAAAAAGGCGGCAGTGGAGGAAGGCA T C AL929236.1,PTPN14 Ensembl:ENSG00000228470,Ensembl:ENSG00000152104 lincRNA,Protein coding intron,3'UTR GSE100210;GSE107867;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;ASD brains,frontal_cortex;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,30559470,32596459 RNA-Seq:(High) rs931744234 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139556,RMVar_hsa_circ_115192 44839 RMVar_ID_44839 Human_SNP_ID_49181244 A-to-I Human chr1 - 214390997 214390997 214390997 CCCCCCATCAGACGCCAGCCCACCTGGAGCCGATCCTCTCTGGTATGTATAGAAGCTGCAGTGAT CCCCCCATCAGACGCCAGCCCACCTGGAGCCGTTCCTCTCTGGTATGTATAGAAGCTGCAGTGAT T A PTPN14 Ensembl:ENSG00000152104 Protein coding CDS GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) 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 44840 RMVar_ID_44840 Human_SNP_ID_49181245 A-to-I Human chr1 - 214390997 214390997 214390997 CCCCCCATCAGACGCCAGCCCACCTGGAGCCGATCCTCTCTGGTATGTATAGAAGCTGCAGTGAT CCCCCCATCAGACGCCAGCCCACCTGGAGCCGGTCCTCTCTGGTATGTATAGAAGCTGCAGTGAT T C PTPN14 Ensembl:ENSG00000152104 Protein coding CDS GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) 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 44841 RMVar_ID_44841 Human_SNP_ID_49189381 A-to-I Human chr1 - 214423967 214423963 214423967 GTTGTTACTGTTTTGTTTTGAAACTGAGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGCGCG GTTGTTACTGTTTTGTTTTGAAACTGAGTCTC____TGTCACCCAGGCTGGAGTGCAGTGGCGCG AGAGT A PTPN14 Ensembl:ENSG00000152104 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs746304873 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_24634523 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 44842 RMVar_ID_44842 Human_SNP_ID_49215006 A-to-I Human chr1 - 214528774 214528774 214528774 GGCATATACCACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGATGGAGTTTCACCATATTGG GGCATATACCACCATGCCTGGCTAATTTTTGTGTTTTTAGTAGAGATGGAGTTTCACCATATTGG T C PTPN14 Ensembl:ENSG00000152104 Protein coding intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs921275688 Functional Loss SNV dbSNP153 33..33 33 - - - 44843 RMVar_ID_44843 Human_SNP_ID_49215444 A-to-I Human chr1 - 214530520 214530520 214530520 CTGGGCAACATGGTGAAACCCCGTCTCTACAAAAAATACAAAAAGTAGCCAGGCATGGTGGTGCA CTGGGCAACATGGTGAAACCCCGTCTCTACAAGAAATACAAAAAGTAGCCAGGCATGGTGGTGCA T C PTPN14 Ensembl:ENSG00000152104 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1370889057 Functional Loss SNV dbSNP153 33..33 33 - - - 44844 RMVar_ID_44844 Human_SNP_ID_49939961 A-to-I Human chr1 - 217454419 217454419 217454419 ACGCCCGGCTAATTTTTTGTATTTTTAGTAGAAACGGGGTTTCACCGTGTTAGCCAGGATGGTCT ACGCCCGGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGGTCT T C GPATCH2 Ensembl:ENSG00000092978 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1015309831 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_100341 RMVar_hsa_circ_289885,RMVar_hsa_circ_366693 44845 RMVar_ID_44845 Human_SNP_ID_49939962 A-to-I Human chr1 - 217454420 217454420 217454420 CACGCCCGGCTAATTTTTTGTATTTTTAGTAGAAACGGGGTTTCACCGTGTTAGCCAGGATGGTC CACGCCCGGCTAATTTTTTGTATTTTTAGTAGGAACGGGGTTTCACCGTGTTAGCCAGGATGGTC T C GPATCH2 Ensembl:ENSG00000092978 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1266431773 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_100341 RMVar_hsa_circ_289885,RMVar_hsa_circ_366693 44846 RMVar_ID_44846 Human_SNP_ID_49940170 A-to-I Human chr1 - 217454829 217454829 217454829 AGGAGTTTGAGACCAGCCTGGCCAATAAGGTGAAACCCCCGTCTCTAGTAAAAATATGAAAATTA AGGAGTTTGAGACCAGCCTGGCCAATAAGGTGGAACCCCCGTCTCTAGTAAAAATATGAAAATTA T C GPATCH2 Ensembl:ENSG00000092978 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1323546738 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_289885,RMVar_hsa_circ_366693 44847 RMVar_ID_44847 Human_SNP_ID_49974852 A-to-I Human chr1 - 217603779 217603779 217603779 GTCTCTACTAAAAATACAAAAATTAGCAGGGCATGGTGATATGTGCCTGTAATCCCAGCTACTAG GTCTCTACTAAAAATACAAAAATTAGCAGGGCTTGGTGATATGTGCCTGTAATCCCAGCTACTAG T A GPATCH2 Ensembl:ENSG00000092978 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs907616256 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 44848 RMVar_ID_44848 Human_SNP_ID_49974853 A-to-I Human chr1 - 217603779 217603779 217603779 GTCTCTACTAAAAATACAAAAATTAGCAGGGCATGGTGATATGTGCCTGTAATCCCAGCTACTAG GTCTCTACTAAAAATACAAAAATTAGCAGGGCGTGGTGATATGTGCCTGTAATCCCAGCTACTAG T C GPATCH2 Ensembl:ENSG00000092978 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs907616256 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 44849 RMVar_ID_44849 Human_SNP_ID_49974881 A-to-I Human chr1 - 217603898 217603898 217603898 CTATTTTGGGCCAGGCACGGTGGCTCACACCTATAATCACAGCACTTTGGGAGGCCAAGGCAGAT CTATTTTGGGCCAGGCACGGTGGCTCACACCTGTAATCACAGCACTTTGGGAGGCCAAGGCAGAT T C GPATCH2 Ensembl:ENSG00000092978 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs556459443 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10774139,Human_RBP_ID_24636778 RMVar_hsa_circ_110936,RMVar_hsa_circ_76851,RMVar_hsa_circ_139613,RMVar_hsa_circ_119353,RMVar_hsa_circ_139614,RMVar_hsa_circ_139615 44850 RMVar_ID_44850 Human_SNP_ID_49974919 A-to-I Human chr1 - 217604092 217604092 217604092 TCCACCTCGCCCTCCCAAAGTACTAGGATTACAGTCGTGAGCCACTGTGCCCGGCCAGAAACTGA TCCACCTCGCCCTCCCAAAGTACTAGGATTACGGTCGTGAGCCACTGTGCCCGGCCAGAAACTGA T C GPATCH2 Ensembl:ENSG00000092978 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215244129 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 44851 RMVar_ID_44851 Human_SNP_ID_49974937 A-to-I Human chr1 - 217604187 217604187 217604187 GCCACTGTGCACTGCTAATTTTTGTATTTTTAATAGAGATGGAGTTTCACCATGTTGGCCAGGCT GCCACTGTGCACTGCTAATTTTTGTATTTTTAGTAGAGATGGAGTTTCACCATGTTGGCCAGGCT T C GPATCH2 Ensembl:ENSG00000092978 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1395476890 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 44852 RMVar_ID_44852 Human_SNP_ID_50149748 A-to-I Human chr1 + 218314737 218314737 218314737 TTTTTTGGCGGGACATGGTGGCTCACATCTGTAATCTCAGCACTTTGGGAGGCCGAGGCAGGCTG TTTTTTGGCGGGACATGGTGGCTCACATCTGTCATCTCAGCACTTTGGGAGGCCGAGGCAGGCTG A C RRP15 Ensembl:ENSG00000067533 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1243614134 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86346,RMVar_hsa_circ_139620,RMVar_hsa_circ_139621,RMVar_hsa_circ_76568 44853 RMVar_ID_44853 Human_SNP_ID_50366050 A-to-I Human chr1 + 219202697 219202697 219202697 AGTGAGGAATGAAGTTAGGTAATTTTTTTTTGAAACAGGGTCTTGCTGTGTTGCCCAGGCTGAAG AGTGAGGAATGAAGTTAGGTAATTTTTTTTTGGAACAGGGTCTTGCTGTGTTGCCCAGGCTGAAG A G LYPLAL1 Ensembl:ENSG00000143353 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1179294807 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9558881,Human_RBP_ID_24637476 Human_miRNA_ID_1949995,Human_miRNA_ID_1951279 RMVar_hsa_circ_40753,RMVar_hsa_circ_266318,RMVar_hsa_circ_139633,RMVar_hsa_circ_105555,RMVar_hsa_circ_139625,RMVar_hsa_circ_139626,RMVar_hsa_circ_139627,RMVar_hsa_circ_127891,RMVar_hsa_circ_139628,RMVar_hsa_circ_139630,RMVar_hsa_circ_139631,RMVar_hsa_circ_139629,RMVar_hsa_circ_98607,RMVar_hsa_circ_139632 44854 RMVar_ID_44854 Human_SNP_ID_50554647 A-to-I Human chr1 - 219970015 219970015 219970015 GAGTTTGAGACCAGCCTGGCCAACATGGCGAAACCCCGTCTCTACTAAAATTACACAAATTAGCT GAGTTTGAGACCAGCCTGGCCAACATGGCGAAGCCCCGTCTCTACTAAAATTACACAAATTAGCT T C EPRS1 Ensembl:ENSG00000136628 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1558267681 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139641,RMVar_hsa_circ_78102,RMVar_hsa_circ_83605,RMVar_hsa_circ_126425,RMVar_hsa_circ_139642,RMVar_hsa_circ_139643,RMVar_hsa_circ_139644,RMVar_hsa_circ_105348 44855 RMVar_ID_44855 Human_SNP_ID_50554783 A-to-I Human chr1 - 219970630 219970630 219970630 GGGATTACAGGCGCCTGCCATGACACGCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTTG GGGATTACAGGCGCCTGCCATGACACGCAGCTGATTTTTGTATTTTTAGTAGAGATGGGGTTTTG T C EPRS1 Ensembl:ENSG00000136628 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs961629337 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139641,RMVar_hsa_circ_78102,RMVar_hsa_circ_83605,RMVar_hsa_circ_126425,RMVar_hsa_circ_139642,RMVar_hsa_circ_139643,RMVar_hsa_circ_139644,RMVar_hsa_circ_105348 44856 RMVar_ID_44856 Human_SNP_ID_50558327 A-to-I Human chr1 - 219984622 219984622 219984622 GGCCAGGAGTTCAAGACTGGCCTGGGCAACATAGCGAGACCCTGCCTCTACCAAAAAATAAAAAT GGCCAGGAGTTCAAGACTGGCCTGGGCAACATGGCGAGACCCTGCCTCTACCAAAAAATAAAAAT T C EPRS1 Ensembl:ENSG00000136628 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1010196164 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72176,RMVar_hsa_circ_83605,RMVar_hsa_circ_139643,RMVar_hsa_circ_115619,RMVar_hsa_circ_20395,RMVar_hsa_circ_57254,RMVar_hsa_circ_52389,RMVar_hsa_circ_57142,RMVar_hsa_circ_139648,RMVar_hsa_circ_362524,RMVar_hsa_circ_139646,RMVar_hsa_circ_314833,RMVar_hsa_circ_139649,RMVar_hsa_circ_5724,RMVar_hsa_circ_34170 44857 RMVar_ID_44857 Human_SNP_ID_50571006 A-to-I Human chr1 - 220035681 220035681 220035681 GGGAGCACAGGTGCATGCCACTATGCCTAGCTAATTTTTGTGTTTTTAGTAGAGACGGGGTTTTA GGGAGCACAGGTGCATGCCACTATGCCTAGCTCATTTTTGTGTTTTTAGTAGAGACGGGGTTTTA T G EPRS1 Ensembl:ENSG00000136628 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1203199736 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266431,RMVar_hsa_circ_70358,RMVar_hsa_circ_139662,RMVar_hsa_circ_336341,RMVar_hsa_circ_35053 44858 RMVar_ID_44858 Human_SNP_ID_50576732 A-to-I Human chr1 - 220057912 220057912 220057912 CGGACTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCACCTGGCCTAAACCAGATTTCTTT CGGACTCCCAAAGTGCTGGGATTACAGGTGTGGGCCACCGCACCTGGCCTAAACCAGATTTCTTT T C BPNT1 Ensembl:ENSG00000162813 Protein coding 3'UTR GSE47997;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829 K562 cells&HepG2 cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line - 23474544,29129909,29796672,31158229 RNA-Seq:(High) rs1251489498 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_341873 Human_Splice_Rec_188910 Human_miRNA_ID_675569,Human_miRNA_ID_999329,Human_miRNA_ID_1143016 44859 RMVar_ID_44859 Human_SNP_ID_50576736 A-to-I Human chr1 - 220057921 220057921 220057921 TGTCTGCCTCGGACTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCACCTGGCCTAAACCA TGTCTGCCTCGGACTCCCAAAGTGCTGGGATTGCAGGTGTGAGCCACCGCACCTGGCCTAAACCA T C BPNT1 Ensembl:ENSG00000162813 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,29129909,31158229,31158229,32596459,32596459 RNA-Seq:(High) rs879012845 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_341873 Human_miRNA_ID_1398426 44860 RMVar_ID_44860 Human_SNP_ID_50576741 A-to-I Human chr1 - 220057933 220057933 220057933 GACATCGTGATCTGTCTGCCTCGGACTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCACC GACATCGTGATCTGTCTGCCTCGGACTCCCAAGGTGCTGGGATTACAGGTGTGAGCCACCGCACC T C BPNT1 Ensembl:ENSG00000162813 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 23474544,24183664,29129909,31158229,31158229 RNA-Seq:(High) rs878938199 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_341873 44861 RMVar_ID_44861 Human_SNP_ID_50576758 A-to-I Human chr1 - 220057956 220057956 220057956 AGCCAGGATGGTCTTGATCTCCTGACATCGTGATCTGTCTGCCTCGGACTCCCAAAGTGCTGGGA AGCCAGGATGGTCTTGATCTCCTGACATCGTGGTCTGTCTGCCTCGGACTCCCAAAGTGCTGGGA T C BPNT1 Ensembl:ENSG00000162813 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1194244965 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_341873,Human_RBP_ID_10779094,Human_RBP_ID_21880960 44862 RMVar_ID_44862 Human_SNP_ID_50576764 A-to-I Human chr1 - 220057984 220057984 220057984 TTTAGTAGAGAAGGTGTTTCACCGTGTTAGCCAGGATGGTCTTGATCTCCTGACATCGTGATCTG TTTAGTAGAGAAGGTGTTTCACCGTGTTAGCCGGGATGGTCTTGATCTCCTGACATCGTGATCTG T C BPNT1 Ensembl:ENSG00000162813 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs528327352 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_341874,Human_RBP_ID_21880960 Human_miRNA_ID_334139 44863 RMVar_ID_44863 Human_SNP_ID_50576768 A-to-I Human chr1 - 220057996 220057996 220057996 ATTTTTTGTATTTTTAGTAGAGAAGGTGTTTCACCGTGTTAGCCAGGATGGTCTTGATCTCCTGA ATTTTTTGTATTTTTAGTAGAGAAGGTGTTTCCCCGTGTTAGCCAGGATGGTCTTGATCTCCTGA T G BPNT1 Ensembl:ENSG00000162813 Protein coding 3'UTR GSE47997;GSE100210;GSE99789;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,29129909,29796672,32596459 RNA-Seq:(High) rs1372728935 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21880960 44864 RMVar_ID_44864 Human_SNP_ID_50576770 A-to-I Human chr1 - 220058010 220058010 220058010 ACCACGCCTGGCTAATTTTTTGTATTTTTAGTAGAGAAGGTGTTTCACCGTGTTAGCCAGGATGG ACCACGCCTGGCTAATTTTTTGTATTTTTAGTGGAGAAGGTGTTTCACCGTGTTAGCCAGGATGG T C BPNT1 Ensembl:ENSG00000162813 Protein coding 3'UTR GSE47997;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 K562 cells&HepG2 cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 23474544,29129909,31158229 RNA-Seq:(High) rs1424536382 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21880960 44865 RMVar_ID_44865 Human_SNP_ID_50576797 A-to-I Human chr1 - 220058113 220058113 220058113 AGAATGTAGTGGCGTGATCTCGGCTCACTGCAAGCTCCGCCTCCCGGGTTCATGCCATTCTCCTG AGAATGTAGTGGCGTGATCTCGGCTCACTGCAGGCTCCGCCTCCCGGGTTCATGCCATTCTCCTG T C BPNT1 Ensembl:ENSG00000162813 Protein coding 3'UTR GSE38233;GSE100210;GSE112787;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;293 Flip-In T-REx cells,empty vector;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,29967493,32596459,32596459 RNA-Seq:(High) rs967028299 Functional Loss SNV dbSNP153 33..33 33 - - - 44866 RMVar_ID_44866 Human_SNP_ID_50576808 A-to-I Human chr1 - 220058142 220058142 220058142 AGACGGAGTCTCGCTCTGTAGCCTAGGCTAGAATGTAGTGGCGTGATCTCGGCTCACTGCAAGCT AGACGGAGTCTCGCTCTGTAGCCTAGGCTAGAGTGTAGTGGCGTGATCTCGGCTCACTGCAAGCT T C BPNT1 Ensembl:ENSG00000162813 Protein coding 3'UTR GSE38233;GSE100210;GSE112787;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;293 Flip-In T-REx cells,empty vector;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,29967493,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs746776724 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_341875,Human_RBP_ID_17739209 44867 RMVar_ID_44867 Human_SNP_ID_50576811 A-to-I Human chr1 - 220058145 220058145 220058145 CTGAGACGGAGTCTCGCTCTGTAGCCTAGGCTAGAATGTAGTGGCGTGATCTCGGCTCACTGCAA CTGAGACGGAGTCTCGCTCTGTAGCCTAGGCTGGAATGTAGTGGCGTGATCTCGGCTCACTGCAA T C BPNT1 Ensembl:ENSG00000162813 Protein coding 3'UTR GSE38233;GSE100210;GSE99789;GSE112787;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;293 Flip-In T-REx cells,empty vector;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,29796672,29967493,31158229,31158229,31158229 RNA-Seq:(High) rs879211031 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_341875,Human_RBP_ID_17739209 44868 RMVar_ID_44868 Human_SNP_ID_50576920 A-to-I Human chr1 - 220058617 220058617 220058617 TGAAGCAGAAGAATCTCTTGAGCCCGGAAGGCAGAGGTTGCAGTGAGCTGAGATCGTGCCACTGC TGAAGCAGAAGAATCTCTTGAGCCCGGAAGGCGGAGGTTGCAGTGAGCTGAGATCGTGCCACTGC T C BPNT1 Ensembl:ENSG00000162813 Protein coding 3'UTR GSE38233;GSE100210;GSE112787 cultured B-cells;HepG2 cell line;293 Flip-In T-REx cells,empty vector - 24183664,29129909,29967493 RNA-Seq:(High) rs3201549 Functional Loss SNV dbSNP153 33..33 33 - - - 44869 RMVar_ID_44869 Human_SNP_ID_50576930 A-to-I Human chr1 - 220058669 220058669 220058669 AAATTAACTGGGCATCCTGTCATGCGCCTGTCATCCCAGCTACTTGAGAGGCTGAAGCAGAAGAA AAATTAACTGGGCATCCTGTCATGCGCCTGTCGTCCCAGCTACTTGAGAGGCTGAAGCAGAAGAA T C BPNT1 Ensembl:ENSG00000162813 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,31158229,32596459,32596459 RNA-Seq:(High) rs1268640885 Functional Loss SNV dbSNP153 33..33 33 - - - 44870 RMVar_ID_44870 Human_SNP_ID_50576946 A-to-I Human chr1 - 220058724 220058724 220058724 AGGAGTTTGAGACCAGCCTGGGCAATATCGTGAGACCCCATCTCTACAAAAATACAAATTAACTG AGGAGTTTGAGACCAGCCTGGGCAATATCGTGTGACCCCATCTCTACAAAAATACAAATTAACTG T A BPNT1 Ensembl:ENSG00000162813 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1045159805 Functional Loss SNV dbSNP153 33..33 33 - - - 44871 RMVar_ID_44871 Human_SNP_ID_50576968 A-to-I Human chr1 - 220058801 220058801 220058801 CATTTGGCCGGGCGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGTGGA CATTTGGCCGGGCGCGGTGGCTCATGCCTGTAGTCCCAGCACTTTGGGAGGCCGAGGCAGGTGGA T C BPNT1 Ensembl:ENSG00000162813 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1137752 Functional Loss SNV dbSNP153 33..33 33 - - - 44872 RMVar_ID_44872 Human_SNP_ID_50576969 A-to-I Human chr1 - 220058802 220058802 220058802 TCATTTGGCCGGGCGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGTGG TCATTTGGCCGGGCGCGGTGGCTCATGCCTGTGATCCCAGCACTTTGGGAGGCCGAGGCAGGTGG T C BPNT1 Ensembl:ENSG00000162813 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs3201546 Functional Loss SNV dbSNP153 33..33 33 - - - 44873 RMVar_ID_44873 Human_SNP_ID_50578701 A-to-I Human chr1 - 220066106 220066106 220066106 AATTGTATTCATTTTCCACAGAACAATGAAAAACAGCAGTTAAGGGAACACAGGAATGAAGCAAA AATTGTATTCATTTTCCACAGAACAATGAAAAGCAGCAGTTAAGGGAACACAGGAATGAAGCAAA T C BPNT1 Ensembl:ENSG00000162813 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1146773 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_188902,Human_Splice_Rec_188903 GWAS_ID_5114,GWAS_ID_5115,GWAS_ID_5116,GWAS_ID_5117 RMVar_hsa_circ_71222 44874 RMVar_ID_44874 Human_SNP_ID_50593087 A-to-I Human chr1 + 220121719 220121719 220121719 CTCCTGCCTTGGCCTCCCAAAGTGCTAGGATTATAGTCATGAGCCACCGTGCCAGGCCAAGAATA CTCCTGCCTTGGCCTCCCAAAGTGCTAGGATTGTAGTCATGAGCCACCGTGCCAGGCCAAGAATA A G IARS2 Ensembl:ENSG00000067704 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs988901793 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24638337 RMVar_hsa_circ_10,RMVar_hsa_circ_121447,RMVar_hsa_circ_89771,RMVar_hsa_circ_139673,RMVar_hsa_circ_12197,RMVar_hsa_circ_121927,RMVar_hsa_circ_139674,RMVar_hsa_circ_139676,RMVar_hsa_circ_126886,RMVar_hsa_circ_312606,RMVar_hsa_circ_139677,RMVar_hsa_circ_45758,RMVar_hsa_circ_18074,RMVar_hsa_circ_139679,RMVar_hsa_circ_281003,RMVar_hsa_circ_312339,RMVar_hsa_circ_62281,RMVar_hsa_circ_330954,RMVar_hsa_circ_300087,RMVar_hsa_circ_272153,RMVar_hsa_circ_139681,RMVar_hsa_circ_139682,RMVar_hsa_circ_139680,RMVar_hsa_circ_139678 44875 RMVar_ID_44875 Human_SNP_ID_50613017 A-to-I Human chr1 - 220205065 220205065 220205065 AATTTTCAGATCTCAATTTCAGAGTTGTGAAAATATGGAAGAGTCTTAAAATCAGTGAAAATACA AATTTTCAGATCTCAATTTCAGAGTTGTGAAACTATGGAAGAGTCTTAAAATCAGTGAAAATACA T G RAB3GAP2 Ensembl:ENSG00000118873 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041302265 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_364943,RMVar_hsa_circ_10596,RMVar_hsa_circ_10755,RMVar_hsa_circ_15336,RMVar_hsa_circ_65479,RMVar_hsa_circ_332723,RMVar_hsa_circ_343238,RMVar_hsa_circ_29330,RMVar_hsa_circ_25197,RMVar_hsa_circ_139702,RMVar_hsa_circ_139701,RMVar_hsa_circ_324618,RMVar_hsa_circ_43696,RMVar_hsa_circ_367062,RMVar_hsa_circ_367519,RMVar_hsa_circ_125804,RMVar_hsa_circ_139703,RMVar_hsa_circ_72965,RMVar_hsa_circ_361930,RMVar_hsa_circ_266004,RMVar_hsa_circ_56231,RMVar_hsa_circ_46948,RMVar_hsa_circ_60134,RMVar_hsa_circ_139708,RMVar_hsa_circ_301148,RMVar_hsa_circ_139712,RMVar_hsa_circ_61615,RMVar_hsa_circ_93132,RMVar_hsa_circ_71518,RMVar_hsa_circ_59354,RMVar_hsa_circ_36655,RMVar_hsa_circ_328394,RMVar_hsa_circ_36238,RMVar_hsa_circ_315940,RMVar_hsa_circ_354470,RMVar_hsa_circ_139713,RMVar_hsa_circ_318547,RMVar_hsa_circ_139714,RMVar_hsa_circ_139715 44876 RMVar_ID_44876 Human_SNP_ID_50626304 A-to-I Human chr1 - 220263683 220263683 220263683 TTTCTGATTTCAAAGCATATTGCAAAGCTGTAATAACCCAAACTGTATGATACTGGCATAAAGAC TTTCTGATTTCAAAGCATATTGCAAAGCTGTAGTAACCCAAACTGTATGATACTGGCATAAAGAC T C RAB3GAP2 Ensembl:ENSG00000118873 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1379512914 Functional Loss SNV dbSNP153 33..33 33 - - - 44877 RMVar_ID_44877 Human_SNP_ID_50626311 A-to-I Human chr1 - 220263719 220263719 220263719 TTTTGGAAAAGAAGAAACAAGTTAGAAGATTCACACTTTCTGATTTCAAAGCATATTGCAAAGCT TTTTGGAAAAGAAGAAACAAGTTAGAAGATTCCCACTTTCTGATTTCAAAGCATATTGCAAAGCT T G RAB3GAP2 Ensembl:ENSG00000118873 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs191219095 Functional Loss SNV dbSNP153 33..33 33 - - - 44878 RMVar_ID_44878 Human_SNP_ID_50675023 A-to-I Human chr1 + 220467992 220467992 220467992 ATCTGGACTTCGGAGCACGTCTTTGACCACCCATAGGAAACTGTTACAACAGCTGCAATGCAGAA ATCTGGACTTCGGAGCACGTCTTTGACCACCCGTAGGAAACTGTTACAACAGCTGCAATGCAGAA A G PRELID3BP1 Ensembl:ENSG00000226226 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs757389142 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17339372,Human_RBP_ID_26375665 Human_miRNA_ID_1835879,Human_miRNA_ID_1838730 44879 RMVar_ID_44879 Human_SNP_ID_50675024 A-to-I Human chr1 + 220467994 220467994 220467994 CTGGACTTCGGAGCACGTCTTTGACCACCCATAGGAAACTGTTACAACAGCTGCAATGCAGAAAT CTGGACTTCGGAGCACGTCTTTGACCACCCATGGGAAACTGTTACAACAGCTGCAATGCAGAAAT A G PRELID3BP1 Ensembl:ENSG00000226226 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1188483438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26375665 Human_miRNA_ID_1823548,Human_miRNA_ID_1835879,Human_miRNA_ID_1838730 44880 RMVar_ID_44880 Human_SNP_ID_50744694 A-to-I Human chr1 + 220764302 220764302 220764302 TTTAGTAGAGATGGGATTTCTCCATGTTGGCCAGGCCAGTCTTGAACTCCTGACCTCAGGTGATC TTTAGTAGAGATGGGATTTCTCCATGTTGGCCGGGCCAGTCTTGAACTCCTGACCTCAGGTGATC A G MTARC2 Ensembl:ENSG00000117791 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1262787869 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139749,RMVar_hsa_circ_338300,RMVar_hsa_circ_139751 44881 RMVar_ID_44881 Human_SNP_ID_50879750 A-to-I Human chr1 - 221330311 221330311 221330311 CACCATCATGCCCAGCTAATTTTTGATTTTTAATAGAGGCAGGGTTTTGCTATATTACCCAGGCT CACCATCATGCCCAGCTAATTTTTGATTTTTAGTAGAGGCAGGGTTTTGCTATATTACCCAGGCT T C LINC02817 Ensembl:ENSG00000234754 lincRNA exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1358099145 Functional Loss SNV dbSNP153 33..33 33 - - - 44882 RMVar_ID_44882 Human_SNP_ID_50880345 A-to-I Human chr1 - 221332941 221332941 221332941 CGTAAACATCACACCTGATCCAACCAATCTGCAGGCCCTACATAAATCAGACACCGCCTCCTCCA CGTAAACATCACACCTGATCCAACCAATCTGCGGGCCCTACATAAATCAGACACCGCCTCCTCCA T C LINC02817 Ensembl:ENSG00000234754 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs4347216 Functional Loss SNV dbSNP153 33..33 33 - - - 44883 RMVar_ID_44883 Human_SNP_ID_50880367 A-to-I Human chr1 - 221333013 221333012 221333013 GGCACTGGCCAAGTGGAAAGGCTGTTTGCATAATAAGATTACGATGGGGTGGCCTGCCTTCCCTG GGCACTGGCCAAGTGGAAAGGCTGTTTGCATA_TAAGATTACGATGGGGTGGCCTGCCTTCCCTG AT A LINC02817 Ensembl:ENSG00000234754 lincRNA exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1377673344 Functional Loss DEL dbSNP153 33..33 33 - - - Human_Splice_Rec_189424,Human_Splice_Rec_189426,Human_Splice_Rec_189430,Human_Splice_Rec_189434,Human_Splice_Rec_189438,Human_Splice_Rec_189442,Human_Splice_Rec_189448,Human_Splice_Rec_189452,Human_Splice_Rec_189456,Human_Splice_Rec_189458 44884 RMVar_ID_44884 Human_SNP_ID_51193122 A-to-I Human chr1 - 222641792 222641792 222641792 TAGAAATGCTCAAGAACCAGCTGGACCAGGAAATGGAGTTCTTGTCCACCTCCATTGCCCAGCTC TAGAAATGCTCAAGAACCAGCTGGACCAGGAAGTGGAGTTCTTGTCCACCTCCATTGCCCAGCTC T C AL592148.1 Ensembl:ENSG00000229399 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878994747 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1421337,Human_RBP_ID_5155920,Human_RBP_ID_8299065,Human_RBP_ID_17340199,Human_RBP_ID_18563480,Human_RBP_ID_26375707 Human_miRNA_ID_1826677,Human_miRNA_ID_2046488 44885 RMVar_ID_44885 Human_SNP_ID_51199409 A-to-I Human chr1 - 222667198 222667198 222667198 TCTTTTCCTGAAGAATTTTTATATTCCTTATGAACTTTGACAGAGTTGTCTTCTTTCAAAGGTCC TCTTTTCCTGAAGAATTTTTATATTCCTTATGGACTTTGACAGAGTTGTCTTCTTTCAAAGGTCC T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs747316172 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8743492 44886 RMVar_ID_44886 Human_SNP_ID_51211185 A-to-I Human chr1 + 222715512 222715512 222715512 GGTGGATCACTTGAGGTCAAGAGTTTGAGACCAGCCTGGCCAACATGGTGAAACCCCGTCTCTAC GGTGGATCACTTGAGGTCAAGAGTTTGAGACCTGCCTGGCCAACATGGTGAAACCCCGTCTCTAC A T BROX Ensembl:ENSG00000162819 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1012377844 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_65968,RMVar_hsa_circ_330924,RMVar_hsa_circ_286453 44887 RMVar_ID_44887 Human_SNP_ID_51257297 A-to-I Human chr1 + 222913660 222913660 222913660 TGGGCATGGTGTCCCACGCTTGTAATACCAGTACTTTGGGAGGCCAAGATGGGAGGATCTCTTGA TGGGCATGGTGTCCCACGCTTGTAATACCAGTGCTTTGGGAGGCCAAGATGGGAGGATCTCTTGA A G DISP1,AC093152.1 Ensembl:ENSG00000154309,Ensembl:ENSG00000278610 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1262911678 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139789,RMVar_hsa_circ_95000,RMVar_hsa_circ_302496 44888 RMVar_ID_44888 Human_SNP_ID_51448832 A-to-I Human chr1 + 223735357 223735357 223735357 CAAGACCAGCTTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCTGGGCA CAAGACCAGCTTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCTGGGCA A G CAPN2 Ensembl:ENSG00000162909 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1350454709 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96606,RMVar_hsa_circ_139806 44889 RMVar_ID_44889 Human_SNP_ID_51448852 A-to-I Human chr1 + 223735421 223735421 223735421 ATGGTGGTGGGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAACCCA ATGGTGGTGGGCGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCTTGAACCCA A G CAPN2 Ensembl:ENSG00000162909 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs137978652 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96606,RMVar_hsa_circ_139806 44890 RMVar_ID_44890 Human_SNP_ID_51451443 A-to-I Human chr1 + 223745433 223745433 223745433 CGAGTTCTGGAGCGCCCTGCTGGAGAAGGCATACGCCAAGTAAGTTGCCATCCTCCCCTGGCCCC CGAGTTCTGGAGCGCCCTGCTGGAGAAGGCATGCGCCAAGTAAGTTGCCATCCTCCCCTGGCCCC A G CAPN2 Ensembl:ENSG00000162909 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749973513 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_743943,Human_RBP_ID_802863,Human_RBP_ID_3934540,Human_RBP_ID_8754371,Human_RBP_ID_26312745 Human_Splice_Rec_190585,Human_Splice_Rec_190625,Human_Splice_Rec_190633 Human_miRNA_ID_2869209 RMVar_hsa_circ_9367,RMVar_hsa_circ_96606,RMVar_hsa_circ_37710,RMVar_hsa_circ_291572,RMVar_hsa_circ_139806,RMVar_hsa_circ_369303,RMVar_hsa_circ_108230,RMVar_hsa_circ_20071,RMVar_hsa_circ_101229,RMVar_hsa_circ_139808,RMVar_hsa_circ_139809,RMVar_hsa_circ_139807,RMVar_hsa_circ_139810 44891 RMVar_ID_44891 Human_SNP_ID_51456925 A-to-I Human chr1 + 223766701 223766701 223766701 CAGGCCCATGGCGGGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGAAGGCCAAGGTGGGCCT CAGGCCCATGGCGGGCGGTGGCTCATGCCTGTGATCCCAGCACTTTGGAAGGCCAAGGTGGGCCT A G CAPN2 Ensembl:ENSG00000162909 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1272129406 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37710,RMVar_hsa_circ_95825,RMVar_hsa_circ_101229,RMVar_hsa_circ_139810,RMVar_hsa_circ_139815,RMVar_hsa_circ_139812,RMVar_hsa_circ_116476,RMVar_hsa_circ_93884,RMVar_hsa_circ_139816,RMVar_hsa_circ_272118,RMVar_hsa_circ_139818,RMVar_hsa_circ_11485,RMVar_hsa_circ_139819,RMVar_hsa_circ_72856,RMVar_hsa_circ_342901 44892 RMVar_ID_44892 Human_SNP_ID_51459103 A-to-I Human chr1 + 223774920 223774920 223774920 ATGATGGAAAATCAGCCAAGGACTAAGCTTCCATAGAAATACACTTTGTATCTGGACCTCAAAAT ATGATGGAAAATCAGCCAAGGACTAAGCTTCCGTAGAAATACACTTTGTATCTGGACCTCAAAAT A G CAPN2 Ensembl:ENSG00000162909 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1157157308 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22716,Human_RBP_ID_342651,Human_RBP_ID_1421472,Human_RBP_ID_1737307,Human_RBP_ID_8743579,Human_RBP_ID_17222028,Human_RBP_ID_17449942,Human_RBP_ID_23366129 Human_Splice_Rec_190618,Human_Splice_Rec_190666,Human_Splice_Rec_190690,Human_Splice_Rec_190708,Human_Splice_Rec_190736 Human_miRNA_ID_2837073,Human_miRNA_ID_2844501,Human_miRNA_ID_2847523,Human_miRNA_ID_2854949 RMVar_hsa_circ_101229,RMVar_hsa_circ_139810 44893 RMVar_ID_44893 Human_SNP_ID_51462886 A-to-I Human chr1 - 223790732 223790732 223790732 AGGTGCGCTGGTGTGTGCCTGTAGTCCCAGCTACCGGGGAGGCTGAGGTGGGAGGATTGCTGGAG AGGTGCGCTGGTGTGTGCCTGTAGTCCCAGCTGCCGGGGAGGCTGAGGTGGGAGGATTGCTGGAG T C TP53BP2 Ensembl:ENSG00000143514 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1311833918 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_368969,RMVar_hsa_circ_271873,RMVar_hsa_circ_139821 44894 RMVar_ID_44894 Human_SNP_ID_51469734 A-to-I Human chr1 - 223818854 223818854 223818854 AAATTTTTGGCCGGACACGGTGGCTGACGCCTATAATCCCAGCACTTTGGGAGGCCAAGGAGGGT AAATTTTTGGCCGGACACGGTGGCTGACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGAGGGT T C TP53BP2 Ensembl:ENSG00000143514 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs541753213 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_276,RMVar_hsa_circ_14697,RMVar_hsa_circ_54914,RMVar_hsa_circ_335186,RMVar_hsa_circ_139835,RMVar_hsa_circ_375660 44895 RMVar_ID_44895 Human_SNP_ID_51475114 A-to-I Human chr1 - 223841079 223841079 223841079 CTCTGCTAATTTTTGTATTTTTTAGTAGAGACAGGGTTTCCCTGTATTGGCCAGGCTGATCTTGA CTCTGCTAATTTTTGTATTTTTTAGTAGAGACGGGGTTTCCCTGTATTGGCCAGGCTGATCTTGA T C TP53BP2 Ensembl:ENSG00000143514 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1308562708 Functional Loss SNV dbSNP153 33..33 33 - - - 44896 RMVar_ID_44896 Human_SNP_ID_51475119 A-to-I Human chr1 - 223841088 223841088 223841088 CAGGCCACGCTCTGCTAATTTTTGTATTTTTTAGTAGAGACAGGGTTTCCCTGTATTGGCCAGGC CAGGCCACGCTCTGCTAATTTTTGTATTTTTTGGTAGAGACAGGGTTTCCCTGTATTGGCCAGGC T C TP53BP2 Ensembl:ENSG00000143514 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041576054 Functional Loss SNV dbSNP153 33..33 33 - - - 44897 RMVar_ID_44897 Human_SNP_ID_51502939 A-to-I Human chr1 - 223959587 223959587 223959587 GGGACTGGGGAGGCTTAGGTTACAGTAAGCTGAGGTTGTGCCACTGCACTCCAGCTTGGACAAAA GGGACTGGGGAGGCTTAGGTTACAGTAAGCTGTGGTTGTGCCACTGCACTCCAGCTTGGACAAAA T A GTF2IP20 Ensembl:ENSG00000272645 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs912783573 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139836,RMVar_hsa_circ_277946 44898 RMVar_ID_44898 Human_SNP_ID_51505505 A-to-I Human chr1 - 223970511 223970511 223970511 CTTCCTCTTTGGCCTCCCAAAATGTTGAGATTACAGATGGGAGCCCCCATACCCACCAATCACAA CTTCCTCTTTGGCCTCCCAAAATGTTGAGATTGCAGATGGGAGCCCCCATACCCACCAATCACAA T C GTF2IP20 Ensembl:ENSG00000272645 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1258449788 Functional Loss SNV dbSNP153 33..33 33 - - - 44899 RMVar_ID_44899 Human_SNP_ID_51513524 A-to-I Human chr1 + 224003518 224003518 224003518 CAACTTAATTGTTTTGTTTATTTGCATTCTATAGCTGGCAGCCTGCTATCAATTACATTGATAGT CAACTTAATTGTTTTGTTTATTTGCATTCTATGGCTGGCAGCCTGCTATCAATTACATTGATAGT A G AC138393.1 Ensembl:ENSG00000185495 Pseudogene intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1284555329 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22561399,Human_RBP_ID_24556128,Human_RBP_ID_24746363 RMVar_hsa_circ_73344 44900 RMVar_ID_44900 Human_SNP_ID_51513823 A-to-I Human chr1 + 224004943 224004943 224004943 ACTGGTCATTTACATTAGGTATTTCTCCTAATACTATCCCTCCCCCATCCTCCATGCCACGACAG ACTGGTCATTTACATTAGGTATTTCTCCTAATCCTATCCCTCCCCCATCCTCCATGCCACGACAG A C AC138393.1 Ensembl:ENSG00000185495 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1290270096 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3334995,Human_RBP_ID_17739902,Human_RBP_ID_18509475,Human_RBP_ID_18930604,Human_RBP_ID_24758263 44901 RMVar_ID_44901 Human_SNP_ID_51545068 A-to-I Human chr1 + 224123987 224123987 224123987 AAAAAATTAGCCGGGCGTGGTGGGAGGTGCCTATAATGCCAACTACTTGGGAGATTGAGGCAGGA AAAAAATTAGCCGGGCGTGGTGGGAGGTGCCTCTAATGCCAACTACTTGGGAGATTGAGGCAGGA A C FBXO28 Ensembl:ENSG00000143756 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs915868490 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24641441 RMVar_hsa_circ_90093,RMVar_hsa_circ_139838 44902 RMVar_ID_44902 Human_SNP_ID_51548041 A-to-I Human chr1 + 224135627 224135627 224135627 GAGCAAGACTCTGTCTCAAAAAAAAAAAAAAAAAAAAAAAAGAAAAAGAAAAAGAAAAATTTAGT GAGCAAGACTCTGTCTCAAAAAAAAAAAAAAAGAAAAAAAAGAAAAAGAAAAAGAAAAATTTAGT A G FBXO28 Ensembl:ENSG00000143756 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1290655574 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90093,RMVar_hsa_circ_69384,RMVar_hsa_circ_139838,RMVar_hsa_circ_122343,RMVar_hsa_circ_139839 44903 RMVar_ID_44903 Human_SNP_ID_51548311 A-to-I Human chr1 + 224136455 224136455 224136455 GGATGTACTTAAAAGTTTAGGCCGGGCGCGGTAGCTCACACCTGTAATCCCAGCACTTTAGGAGG GGATGTACTTAAAAGTTTAGGCCGGGCGCGGTGGCTCACACCTGTAATCCCAGCACTTTAGGAGG A G FBXO28 Ensembl:ENSG00000143756 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs919562737 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_803226 RMVar_hsa_circ_90093,RMVar_hsa_circ_69384,RMVar_hsa_circ_139838,RMVar_hsa_circ_122343,RMVar_hsa_circ_139839 44904 RMVar_ID_44904 Human_SNP_ID_51561238 A-to-I Human chr1 + 224184695 224184692 224184696 CACTACGCCTGGCTAATGTTTGTATCTTTTTTAGTTAGAGACGGGGTTTCACCATGTTGGCCAGG CACTACGCCTGGCTAATGTTTGTATCTTTT____TTAGAGACGGGGTTTCACCATGTTGGCCAGG TTTAG T DEGS1 Ensembl:ENSG00000143753 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1222979152 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_10792506 44905 RMVar_ID_44905 Human_SNP_ID_51561662 A-to-I Human chr1 + 224186119 224186119 224186119 GAACTCAGGAGTTCGAGGCCAACCTGGGCAACATGGCAAAACCCCATCTCTACCAAAAAAAAAAA GAACTCAGGAGTTCGAGGCCAACCTGGGCAACGTGGCAAAACCCCATCTCTACCAAAAAAAAAAA A G DEGS1 Ensembl:ENSG00000143753 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1429088109 Functional Loss SNV dbSNP153 33..33 33 - - - 44906 RMVar_ID_44906 Human_SNP_ID_51561833 A-to-I Human chr1 + 224186606 224186606 224186606 GTGGCGGCAGCCACCTGTAGTCCCAACTACTCAGGAGGCCGAGGCAGGAGAATGGCGTGAACCCG GTGGCGGCAGCCACCTGTAGTCCCAACTACTCGGGAGGCCGAGGCAGGAGAATGGCGTGAACCCG A G DEGS1 Ensembl:ENSG00000143753 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1293243673 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_101649 44907 RMVar_ID_44907 Human_SNP_ID_51561991 A-to-I Human chr1 + 224187161 224187161 224187161 GAAACCCCGTCTCTACTAAAAATACAAAAATTAGCTGGGTGTGGTGGTGGGCGCCTGTAATCCCA GAAACCCCGTCTCTACTAAAAATACAAAAATTGGCTGGGTGTGGTGGTGGGCGCCTGTAATCCCA A G DEGS1 Ensembl:ENSG00000143753 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1377574855 Functional Loss SNV dbSNP153 33..33 33 - - - 44908 RMVar_ID_44908 Human_SNP_ID_51562060 A-to-I Human chr1 + 224187398 224187398 224187398 ATACAGCTTTTTAATGTTTTATTTTTTGAGAGAGAGTCTCACTGTGTTGCCCAGGCTGGAGTGCA ATACAGCTTTTTAATGTTTTATTTTTTGAGAGTGAGTCTCACTGTGTTGCCCAGGCTGGAGTGCA A T DEGS1 Ensembl:ENSG00000143753 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs749246814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9489758,Human_RBP_ID_24758328 44909 RMVar_ID_44909 Human_SNP_ID_51562802 A-to-I Human chr1 + 224190389 224190385 224190389 TTTCATTTGTTTGTTTTTTGAGACGGTGTCTCACTCAGTCGCCCAGGCTGGCGGGCAGTGGCACG TTTCATTTGTTTGTTTTTTGAGACGGTGT____CTCAGTCGCCCAGGCTGGCGGGCAGTGGCACG TCTCA T DEGS1 Ensembl:ENSG00000143753 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1469312471 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_139842,RMVar_hsa_circ_139843 44910 RMVar_ID_44910 Human_SNP_ID_51563464 A-to-I Human chr1 + 224192796 224192796 224192796 AGCTATTTCGCCAGGCACGGTGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCCAAGGTGGGT AGCTATTTCGCCAGGCACGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGT A G DEGS1 Ensembl:ENSG00000143753 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1394127357 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_342906 RMVar_hsa_circ_139843 44911 RMVar_ID_44911 Human_SNP_ID_51563683 A-to-I Human chr1 + 224193693 224193693 224193693 ATCAGCAGCTGGGTGTGGTGGTTCACACCTGTAATTCCATGCTTCGGAAAGCTGAGGCAGGAGGA ATCAGCAGCTGGGTGTGGTGGTTCACACCTGTGATTCCATGCTTCGGAAAGCTGAGGCAGGAGGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1029869486 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5763052 RMVar_hsa_circ_139843 44912 RMVar_ID_44912 Human_SNP_ID_51573271 A-to-I Human chr1 - 224229970 224229970 224229970 AAACTTAGCCAGGCATGGTGTCATGCACCTGTAGTCCCAGCTACTTAGGAGACCGAGGCAGAAGG AAACTTAGCCAGGCATGGTGTCATGCACCTGTGGTCCCAGCTACTTAGGAGACCGAGGCAGAAGG T C NVL Ensembl:ENSG00000143748 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1199547609 Functional Loss SNV dbSNP153 33..33 33 - - - 44913 RMVar_ID_44913 Human_SNP_ID_51579013 A-to-I Human chr1 - 224253131 224253131 224253131 CTGATGCAGAGAACTGCTTGAACCCAGGAGGCAGAGGTTGCAATGAGCCGAGATCGCCCCACTGC CTGATGCAGAGAACTGCTTGAACCCAGGAGGCGGAGGTTGCAATGAGCCGAGATCGCCCCACTGC T C NVL Ensembl:ENSG00000143748 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1349453239 Functional Loss SNV dbSNP153 33..33 33 - - - 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 44914 RMVar_ID_44914 Human_SNP_ID_51579014 A-to-I Human chr1 - 224253138 224253138 224253138 TGGGAGGCTGATGCAGAGAACTGCTTGAACCCAGGAGGCAGAGGTTGCAATGAGCCGAGATCGCC TGGGAGGCTGATGCAGAGAACTGCTTGAACCCGGGAGGCAGAGGTTGCAATGAGCCGAGATCGCC T C NVL Ensembl:ENSG00000143748 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1430793054 Functional Loss SNV dbSNP153 33..33 33 - - - 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 44915 RMVar_ID_44915 Human_SNP_ID_51580994 A-to-I Human chr1 - 224260423 224260423 224260423 TGAAACCCGTCTCTACTGAAAATACAAAAATTAGCTGGCCATGGTGGCGCGTGCCTGTAGTCCCA TGAAACCCGTCTCTACTGAAAATACAAAAATTGGCTGGCCATGGTGGCGCGTGCCTGTAGTCCCA T C NVL Ensembl:ENSG00000143748 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1279769493 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9489880,Human_RBP_ID_22873773,Human_RBP_ID_24642077 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 44916 RMVar_ID_44916 Human_SNP_ID_51581163 A-to-I Human chr1 - 224261016 224261016 224261016 AAAAAATCAGCTGGGCGTGGTAGCACGTGCCCATAGTCCCAGCTACTCGGGAGGCTGAGGCAGAA AAAAAATCAGCTGGGCGTGGTAGCACGTGCCCGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGAA T C NVL Ensembl:ENSG00000143748 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs761026194 Functional Loss SNV dbSNP153 33..33 33 - - - 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 44917 RMVar_ID_44917 Human_SNP_ID_51581325 A-to-I Human chr1 - 224261786 224261786 224261786 CAGCTAATTAAAAAAAAAAAAAACTTTTTTGTAGAGATGACGTCTCACTATGTTGCCCAGGCTGG CAGCTAATTAAAAAAAAAAAAAACTTTTTTGTGGAGATGACGTCTCACTATGTTGCCCAGGCTGG T C NVL Ensembl:ENSG00000143748 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1029880282 Functional Loss SNV dbSNP153 33..33 33 - - - 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 44918 RMVar_ID_44918 Human_SNP_ID_51582136 A-to-I Human chr1 - 224265452 224265452 224265452 CTGCCCAGGCTGGAGTGCAGTGGTGTGATCTCAGCTCCTTGCAACCTCTGCCTCCTGGGTTCAAA CTGCCCAGGCTGGAGTGCAGTGGTGTGATCTCGGCTCCTTGCAACCTCTGCCTCCTGGGTTCAAA T C NVL Ensembl:ENSG00000143748 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1320493106 Functional Loss SNV dbSNP153 33..33 33 - - - 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 44919 RMVar_ID_44919 Human_SNP_ID_51582246 A-to-I Human chr1 - 224265924 224265924 224265924 ATTAAAAAAGAAAGAAAGTGGCCAAGCTGGGCATGGTGGCTTATGCCTGTAATCCTAGCACTTTA ATTAAAAAAGAAAGAAAGTGGCCAAGCTGGGCGTGGTGGCTTATGCCTGTAATCCTAGCACTTTA T C NVL Ensembl:ENSG00000143748 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904020395 Functional Loss SNV dbSNP153 33..33 33 - - - 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 44920 RMVar_ID_44920 Human_SNP_ID_51582794 A-to-I Human chr1 - 224268611 224268611 224268611 TTAGTCTTGGTGGGGTGCAGCGGCTCACACCTATAATCCCAGCACTTTGGGAGGCTGAGGCAAGA TTAGTCTTGGTGGGGTGCAGCGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAAGA T C NVL Ensembl:ENSG00000143748 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1040058507 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3109,RMVar_hsa_circ_127551,RMVar_hsa_circ_342510,RMVar_hsa_circ_117757,RMVar_hsa_circ_58648,RMVar_hsa_circ_139849,RMVar_hsa_circ_139850,RMVar_hsa_circ_139851,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_64648,RMVar_hsa_circ_354419,RMVar_hsa_circ_139852,RMVar_hsa_circ_332590,RMVar_hsa_circ_51516,RMVar_hsa_circ_139856 44921 RMVar_ID_44921 Human_SNP_ID_51582796 A-to-I Human chr1 - 224268615 224268615 224268615 AAGCTTAGTCTTGGTGGGGTGCAGCGGCTCACACCTATAATCCCAGCACTTTGGGAGGCTGAGGC AAGCTTAGTCTTGGTGGGGTGCAGCGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCTGAGGC T C NVL Ensembl:ENSG00000143748 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs929450349 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3109,RMVar_hsa_circ_127551,RMVar_hsa_circ_342510,RMVar_hsa_circ_117757,RMVar_hsa_circ_58648,RMVar_hsa_circ_139849,RMVar_hsa_circ_139850,RMVar_hsa_circ_139851,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_64648,RMVar_hsa_circ_354419,RMVar_hsa_circ_139852,RMVar_hsa_circ_332590,RMVar_hsa_circ_51516,RMVar_hsa_circ_139856 44922 RMVar_ID_44922 Human_SNP_ID_51583415 A-to-I Human chr1 - 224271327 224271327 224271327 GCACCACCACACCCAGCTAAGTTTTTGTTTTTAGAGGTGGGATCTTGCTGTGTTGCCCAGGCTTG GCACCACCACACCCAGCTAAGTTTTTGTTTTTGGAGGTGGGATCTTGCTGTGTTGCCCAGGCTTG T C NVL Ensembl:ENSG00000143748 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1208208477 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5763309,Human_RBP_ID_11198243 RMVar_hsa_circ_3109,RMVar_hsa_circ_127551,RMVar_hsa_circ_342510,RMVar_hsa_circ_117757,RMVar_hsa_circ_58648,RMVar_hsa_circ_139849,RMVar_hsa_circ_139850,RMVar_hsa_circ_139851,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_64648,RMVar_hsa_circ_354419,RMVar_hsa_circ_139852,RMVar_hsa_circ_332590,RMVar_hsa_circ_51516,RMVar_hsa_circ_139856 44923 RMVar_ID_44923 Human_SNP_ID_51585991 A-to-I Human chr1 - 224281787 224281787 224281787 CACCATGCCCGACTAATTTTTGTGTTTTTAGTAGAGATGGGGTTTCACCATATTGGTCAGGCTGG CACCATGCCCGACTAATTTTTGTGTTTTTAGTGGAGATGGGGTTTCACCATATTGGTCAGGCTGG T C NVL Ensembl:ENSG00000143748 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1184564211 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127551,RMVar_hsa_circ_342510,RMVar_hsa_circ_117757,RMVar_hsa_circ_58648,RMVar_hsa_circ_139849,RMVar_hsa_circ_139850,RMVar_hsa_circ_139851,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_64648,RMVar_hsa_circ_139852,RMVar_hsa_circ_332590,RMVar_hsa_circ_51516,RMVar_hsa_circ_33900,RMVar_hsa_circ_8359,RMVar_hsa_circ_139856,RMVar_hsa_circ_328152,RMVar_hsa_circ_325224,RMVar_hsa_circ_139859,RMVar_hsa_circ_139860,RMVar_hsa_circ_302032,RMVar_hsa_circ_342537,RMVar_hsa_circ_349154,RMVar_hsa_circ_98839,RMVar_hsa_circ_139861,RMVar_hsa_circ_1963,RMVar_hsa_circ_17076,RMVar_hsa_circ_139862 44924 RMVar_ID_44924 Human_SNP_ID_51586228 A-to-I Human chr1 - 224282741 224282741 224282741 TTTGGAAGAATAAGAATTGGGAGTCCAGTTTTAGAAGTGGTAGATTTGAAATGCTTGTGCAATCC TTTGGAAGAATAAGAATTGGGAGTCCAGTTTTGGAAGTGGTAGATTTGAAATGCTTGTGCAATCC T C NVL Ensembl:ENSG00000143748 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10799558 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127551,RMVar_hsa_circ_342510,RMVar_hsa_circ_117757,RMVar_hsa_circ_58648,RMVar_hsa_circ_139849,RMVar_hsa_circ_139850,RMVar_hsa_circ_139851,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_64648,RMVar_hsa_circ_139852,RMVar_hsa_circ_332590,RMVar_hsa_circ_51516,RMVar_hsa_circ_33900,RMVar_hsa_circ_8359,RMVar_hsa_circ_139856,RMVar_hsa_circ_328152,RMVar_hsa_circ_325224,RMVar_hsa_circ_139859,RMVar_hsa_circ_139860,RMVar_hsa_circ_302032,RMVar_hsa_circ_342537,RMVar_hsa_circ_349154,RMVar_hsa_circ_98839,RMVar_hsa_circ_139861,RMVar_hsa_circ_1963,RMVar_hsa_circ_17076,RMVar_hsa_circ_139862 44925 RMVar_ID_44925 Human_SNP_ID_51593321 A-to-I Human chr1 - 224312885 224312880 224312885 ATTCATATAAAGCTTTCTACCTAAAAAAAAAAAAAAATTATTTAAATAAGAAAAGGGCTTTTTTT ATTCATATAAAGCTTTCTACCTAAAAAAAAAA_____TTATTTAAATAAGAAAAGGGCTTTTTTT ATTTTT A NVL Ensembl:ENSG00000143748 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1159514298 Functional Loss DEL dbSNP153 33..37 33 - - - RMVar_hsa_circ_58648,RMVar_hsa_circ_73989,RMVar_hsa_circ_4043,RMVar_hsa_circ_98839,RMVar_hsa_circ_139862,RMVar_hsa_circ_50721,RMVar_hsa_circ_71691,RMVar_hsa_circ_60869,RMVar_hsa_circ_88659,RMVar_hsa_circ_139868,RMVar_hsa_circ_74461,RMVar_hsa_circ_69288,RMVar_hsa_circ_337789,RMVar_hsa_circ_378893,RMVar_hsa_circ_139871,RMVar_hsa_circ_60607 44926 RMVar_ID_44926 Human_SNP_ID_51593322 A-to-I Human chr1 - 224312885 224312880 224312885 ATTCATATAAAGCTTTCTACCTAAAAAAAAAAAAAAATTATTTAAATAAGAAAAGGGCTTTTTTT ATTCATATAAAGCTTTCTACCTAAAAAAAAAA____ATTATTTAAATAAGAAAAGGGCTTTTTTT ATTTTT AT NVL Ensembl:ENSG00000143748 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1159514298 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_58648,RMVar_hsa_circ_73989,RMVar_hsa_circ_4043,RMVar_hsa_circ_98839,RMVar_hsa_circ_139862,RMVar_hsa_circ_50721,RMVar_hsa_circ_71691,RMVar_hsa_circ_60869,RMVar_hsa_circ_88659,RMVar_hsa_circ_139868,RMVar_hsa_circ_74461,RMVar_hsa_circ_69288,RMVar_hsa_circ_337789,RMVar_hsa_circ_378893,RMVar_hsa_circ_139871,RMVar_hsa_circ_60607 44927 RMVar_ID_44927 Human_SNP_ID_51593323 A-to-I Human chr1 - 224312885 224312880 224312885 ATTCATATAAAGCTTTCTACCTAAAAAAAAAAAAAAATTATTTAAATAAGAAAAGGGCTTTTTTT ATTCATATAAAGCTTTCTACCTAAAAAAAAAA__AAATTATTTAAATAAGAAAAGGGCTTTTTTT ATTTTT ATTT NVL Ensembl:ENSG00000143748 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1159514298 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_58648,RMVar_hsa_circ_73989,RMVar_hsa_circ_4043,RMVar_hsa_circ_98839,RMVar_hsa_circ_139862,RMVar_hsa_circ_50721,RMVar_hsa_circ_71691,RMVar_hsa_circ_60869,RMVar_hsa_circ_88659,RMVar_hsa_circ_139868,RMVar_hsa_circ_74461,RMVar_hsa_circ_69288,RMVar_hsa_circ_337789,RMVar_hsa_circ_378893,RMVar_hsa_circ_139871,RMVar_hsa_circ_60607 44928 RMVar_ID_44928 Human_SNP_ID_51593324 A-to-I Human chr1 - 224312885 224312880 224312885 ATTCATATAAAGCTTTCTACCTAAAAAAAAAAAAAAATTATTTAAATAAGAAAAGGGCTTTTTTT ATTCATATAAAGCTTTCTACCTAAAAAAAAAA_AAAATTATTTAAATAAGAAAAGGGCTTTTTTT ATTTTT ATTTT NVL Ensembl:ENSG00000143748 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1159514298 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_58648,RMVar_hsa_circ_73989,RMVar_hsa_circ_4043,RMVar_hsa_circ_98839,RMVar_hsa_circ_139862,RMVar_hsa_circ_50721,RMVar_hsa_circ_71691,RMVar_hsa_circ_60869,RMVar_hsa_circ_88659,RMVar_hsa_circ_139868,RMVar_hsa_circ_74461,RMVar_hsa_circ_69288,RMVar_hsa_circ_337789,RMVar_hsa_circ_378893,RMVar_hsa_circ_139871,RMVar_hsa_circ_60607 44929 RMVar_ID_44929 Human_SNP_ID_51593329 A-to-I Human chr1 - 224312890 224312890 224312890 ATTGCATTCATATAAAGCTTTCTACCTAAAAAAAAAAAAAAATTATTTAAATAAGAAAAGGGCTT ATTGCATTCATATAAAGCTTTCTACCTAAAAAGAAAAAAAAATTATTTAAATAAGAAAAGGGCTT T C NVL Ensembl:ENSG00000143748 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs200958142 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58648,RMVar_hsa_circ_73989,RMVar_hsa_circ_4043,RMVar_hsa_circ_98839,RMVar_hsa_circ_139862,RMVar_hsa_circ_50721,RMVar_hsa_circ_71691,RMVar_hsa_circ_60869,RMVar_hsa_circ_88659,RMVar_hsa_circ_139868,RMVar_hsa_circ_74461,RMVar_hsa_circ_69288,RMVar_hsa_circ_337789,RMVar_hsa_circ_378893,RMVar_hsa_circ_139871,RMVar_hsa_circ_60607 44930 RMVar_ID_44930 Human_SNP_ID_51596097 A-to-I Human chr1 - 224324633 224324633 224324633 GCCATAGAGTTCAAGACCAACTTGGGGAACATAGTGAGACCCCATCTCTACAAAATGAAAATAGA GCCATAGAGTTCAAGACCAACTTGGGGAACATTGTGAGACCCCATCTCTACAAAATGAAAATAGA T A NVL Ensembl:ENSG00000143748 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs898542685 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73989,RMVar_hsa_circ_4043,RMVar_hsa_circ_50721,RMVar_hsa_circ_60869,RMVar_hsa_circ_88659,RMVar_hsa_circ_139868,RMVar_hsa_circ_74461,RMVar_hsa_circ_69288,RMVar_hsa_circ_139873,RMVar_hsa_circ_313730 44931 RMVar_ID_44931 Human_SNP_ID_51596108 A-to-I Human chr1 - 224324689 224324689 224324689 CAGATGCAAGGACTCACACCTATAATCCCAGCATTTTGAGGGGCCATTGGCTTAAGGCCATAGAG CAGATGCAAGGACTCACACCTATAATCCCAGCGTTTTGAGGGGCCATTGGCTTAAGGCCATAGAG T C NVL Ensembl:ENSG00000143748 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2404860 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73989,RMVar_hsa_circ_4043,RMVar_hsa_circ_50721,RMVar_hsa_circ_60869,RMVar_hsa_circ_88659,RMVar_hsa_circ_139868,RMVar_hsa_circ_74461,RMVar_hsa_circ_69288,RMVar_hsa_circ_139873,RMVar_hsa_circ_313730 44932 RMVar_ID_44932 Human_SNP_ID_51607697 A-to-I Human chr1 + 224369496 224369496 224369496 TACTCCGCAGCCTGAGGCAGGAGAATTGCTTGAATCCAGGAGGAGGAGGTTGCGCTGAGCCGAGA TACTCCGCAGCCTGAGGCAGGAGAATTGCTTGCATCCAGGAGGAGGAGGTTGCGCTGAGCCGAGA A C CNIH4 Ensembl:ENSG00000143771 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1434925459 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139876,RMVar_hsa_circ_124045,RMVar_hsa_circ_290411,RMVar_hsa_circ_139877,RMVar_hsa_circ_139874,RMVar_hsa_circ_139875 44933 RMVar_ID_44933 Human_SNP_ID_51608739 A-to-I Human chr1 + 224373783 224373783 224373783 CCGGGAGGTGGAGGTTGCGGTGAGCCGATATCATGCCACTGCACTGCAGCCTGGGTGACAGAGTA CCGGGAGGTGGAGGTTGCGGTGAGCCGATATCGTGCCACTGCACTGCAGCCTGGGTGACAGAGTA A G CNIH4 Ensembl:ENSG00000143771 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1331313755 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_97754,Human_RBP_ID_9490208,Human_RBP_ID_22855283,Human_RBP_ID_24758498 RMVar_hsa_circ_139876,RMVar_hsa_circ_124045,RMVar_hsa_circ_139874,RMVar_hsa_circ_139875 44934 RMVar_ID_44934 Human_SNP_ID_51614087 A-to-I Human chr1 - 224396881 224396881 224396881 TTCTTTTCTTTTCTTTTCTTTTTTTGAGTGCAATGGCACGATCTTGATGCAACCTCCACCTCCTG TTCTTTTCTTTTCTTTTCTTTTTTTGAGTGCAGTGGCACGATCTTGATGCAACCTCCACCTCCTG T C WDR26 Ensembl:ENSG00000162923 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1299664208 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10796648,Human_RBP_ID_19282055 RMVar_hsa_circ_119423,RMVar_hsa_circ_340235,RMVar_hsa_circ_354059,RMVar_hsa_circ_360989,RMVar_hsa_circ_376039,RMVar_hsa_circ_345405,RMVar_hsa_circ_315235,RMVar_hsa_circ_335252,RMVar_hsa_circ_308502,RMVar_hsa_circ_139882,RMVar_hsa_circ_4093,RMVar_hsa_circ_57943,RMVar_hsa_circ_139884,RMVar_hsa_circ_139885,RMVar_hsa_circ_139883,RMVar_hsa_circ_139880,RMVar_hsa_circ_139881 44935 RMVar_ID_44935 Human_SNP_ID_51614769 A-to-I Human chr1 - 224399941 224399941 224399941 GAGACAGGGTCTTGCTCTCTGCCACCCATGCTAGAGTACATTGGTGTGATCATGGCTCACTGCAG GAGACAGGGTCTTGCTCTCTGCCACCCATGCTTGAGTACATTGGTGTGATCATGGCTCACTGCAG T A WDR26 Ensembl:ENSG00000162923 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1176186408 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44224,RMVar_hsa_circ_119423,RMVar_hsa_circ_340235,RMVar_hsa_circ_354059,RMVar_hsa_circ_360989,RMVar_hsa_circ_315235,RMVar_hsa_circ_335252,RMVar_hsa_circ_308502,RMVar_hsa_circ_139882,RMVar_hsa_circ_4093,RMVar_hsa_circ_57943,RMVar_hsa_circ_139884,RMVar_hsa_circ_139883,RMVar_hsa_circ_309199,RMVar_hsa_circ_139880,RMVar_hsa_circ_139881,RMVar_hsa_circ_326315,RMVar_hsa_circ_310033,RMVar_hsa_circ_300897,RMVar_hsa_circ_61902,RMVar_hsa_circ_27780,RMVar_hsa_circ_73690,RMVar_hsa_circ_105633,RMVar_hsa_circ_139887,RMVar_hsa_circ_364774,RMVar_hsa_circ_91491,RMVar_hsa_circ_139888,RMVar_hsa_circ_139889,RMVar_hsa_circ_373536,RMVar_hsa_circ_373930,RMVar_hsa_circ_59861,RMVar_hsa_circ_139890,RMVar_hsa_circ_11254,RMVar_hsa_circ_26004,RMVar_hsa_circ_139891 44936 RMVar_ID_44936 Human_SNP_ID_51615812 A-to-I Human chr1 - 224403911 224403911 224403911 TGTTTTTGAGACAGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCGGTGGCGCAATCTCGGCTCAC TGTTTTTGAGACAGAGTCTCGCTCTGTCGCCCGGGCTGGAGTGCGGTGGCGCAATCTCGGCTCAC T C WDR26 Ensembl:ENSG00000162923 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1254074257 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6805,RMVar_hsa_circ_44224,RMVar_hsa_circ_119423,RMVar_hsa_circ_340235,RMVar_hsa_circ_354059,RMVar_hsa_circ_360989,RMVar_hsa_circ_315235,RMVar_hsa_circ_308502,RMVar_hsa_circ_139882,RMVar_hsa_circ_4093,RMVar_hsa_circ_57943,RMVar_hsa_circ_139883,RMVar_hsa_circ_309199,RMVar_hsa_circ_139880,RMVar_hsa_circ_139881,RMVar_hsa_circ_326315,RMVar_hsa_circ_300897,RMVar_hsa_circ_61902,RMVar_hsa_circ_27780,RMVar_hsa_circ_105633,RMVar_hsa_circ_364774,RMVar_hsa_circ_91491,RMVar_hsa_circ_139888,RMVar_hsa_circ_139889,RMVar_hsa_circ_373536,RMVar_hsa_circ_373930,RMVar_hsa_circ_139890,RMVar_hsa_circ_11254,RMVar_hsa_circ_26004,RMVar_hsa_circ_139891,RMVar_hsa_circ_64892,RMVar_hsa_circ_339388,RMVar_hsa_circ_346669,RMVar_hsa_circ_357811,RMVar_hsa_circ_301018,RMVar_hsa_circ_58199,RMVar_hsa_circ_139892,RMVar_hsa_circ_33677 44937 RMVar_ID_44937 Human_SNP_ID_51618007 A-to-I Human chr1 - 224411784 224411784 224411784 GGAGAGTCTCTTGACCCCAGGCGGTCAGGGCTACAGTGATCTATGATTGTGCTACTGTACAACAG GGAGAGTCTCTTGACCCCAGGCGGTCAGGGCTGCAGTGATCTATGATTGTGCTACTGTACAACAG T C WDR26 Ensembl:ENSG00000162923 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-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 44938 RMVar_ID_44938 Human_SNP_ID_51628375 A-to-I Human chr1 + 224453449 224453449 224453449 GGCTCAAGTGATCCTCCCACTTTGGCCTCCCAAAGTGTTGGGGTTACAGACGTGAGCCACTCTAC GGCTCAAGTGATCCTCCCACTTTGGCCTCCCAGAGTGTTGGGGTTACAGACGTGAGCCACTCTAC A G CNIH3 Ensembl:ENSG00000143786 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs755045237 Functional Loss SNV dbSNP153 33..33 33 - - - 44939 RMVar_ID_44939 Human_SNP_ID_51638819 A-to-I Human chr1 + 224500198 224500198 224500198 ACTAATTAAAACAATTTTTTTTTTTTATAGAGATAGTGTCTCCTTATGTTGCTCAGACTGGTCTC ACTAATTAAAACAATTTTTTTTTTTTATAGAGGTAGTGTCTCCTTATGTTGCTCAGACTGGTCTC A G CNIH3 Ensembl:ENSG00000143786 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1391666033 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_139908,RMVar_hsa_circ_328296 44940 RMVar_ID_44940 Human_SNP_ID_51655730 A-to-I Human chr1 + 224575128 224575128 224575128 CTGGGCCAAGCCTGAGGACCCTTCCCTCCTGGAAGATCCCAGGATCAAGGCGATCACAGCCAAAC CTGGGCCAAGCCTGAGGACCCTTCCCTCCTGGGAGATCCCAGGATCAAGGCGATCACAGCCAAAC A G CNIH3,AKR1B1P1 Ensembl:ENSG00000143786,Ensembl:ENSG00000229991 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1180198646 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21902,RMVar_hsa_circ_8842 44941 RMVar_ID_44941 Human_SNP_ID_51739245 A-to-I Human chr1 + 224938847 224938847 224938847 GAAAATGTGGTATATATACAAAATGGAATACTATTCAGCTGTAAAAAAGAACCCTGTCGTTTACG GAAAATGTGGTATATATACAAAATGGAATACTGTTCAGCTGTAAAAAAGAACCCTGTCGTTTACG A G DNAH14 Ensembl:ENSG00000185842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1426374935 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1737895,Human_RBP_ID_2125747,Human_RBP_ID_8228113 44942 RMVar_ID_44942 Human_SNP_ID_301464249 A-to-I Human chr6 + 150797022 150797018 150797022 TGTTTTGTTTTGTTTTTTTGAGACAGAGTCTCACTCCGCCACCCAGGCTGGAGTGCAGTGGCGCG TGTTTTGTTTTGTTTTTTTGAGACAGAGT____CTCCGCCACCCAGGCTGGAGTGCAGTGGCGCG TCTCA T PLEKHG1 Ensembl:ENSG00000120278 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1056814131 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_7559479 RMVar_hsa_circ_68102,RMVar_hsa_circ_67832,RMVar_hsa_circ_57320,RMVar_hsa_circ_291894,RMVar_hsa_circ_354036,RMVar_hsa_circ_242287,RMVar_hsa_circ_59429,RMVar_hsa_circ_283489,RMVar_hsa_circ_323803,RMVar_hsa_circ_268939,RMVar_hsa_circ_242288,RMVar_hsa_circ_242286 44943 RMVar_ID_44943 Human_SNP_ID_301482305 A-to-I Human chr6 + 150867316 150867316 150867316 TGGGCTCAAGCGATTCTCCCGCCTTAGCCTCCAGTGTAACTGGGACCACAGGTGTGCGCTACCAT TGGGCTCAAGCGATTCTCCCGCCTTAGCCTCCGGTGTAACTGGGACCACAGGTGTGCGCTACCAT A G MTHFD1L Ensembl:ENSG00000120254 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1241282283 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_242293,RMVar_hsa_circ_75615 44944 RMVar_ID_44944 Human_SNP_ID_301484423 A-to-I Human chr6 + 150875155 150875155 150875155 ATAGCTTACTACAGCCTCAAACTCATGGGCTCAAGCGGTCCTCCAGCTTCAGCCTCCCAAGTATC ATAGCTTACTACAGCCTCAAACTCATGGGCTCGAGCGGTCCTCCAGCTTCAGCCTCCCAAGTATC A G MTHFD1L Ensembl:ENSG00000120254 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs974487237 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_242293,RMVar_hsa_circ_75615 44945 RMVar_ID_44945 Human_SNP_ID_301490155 A-to-I Human chr6 + 150898931 150898931 150898931 GTGATCTAGGCTCACTGCAAGCTCTGCCTCCCAGGTTGAAGTGATTCTCCTGTGAAAGGGAATTA GTGATCTAGGCTCACTGCAAGCTCTGCCTCCCGGGTTGAAGTGATTCTCCTGTGAAAGGGAATTA A G MTHFD1L Ensembl:ENSG00000120254 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1268809256 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9189718 Human_Splice_Rec_822846 RMVar_hsa_circ_27359,RMVar_hsa_circ_335989,RMVar_hsa_circ_242293,RMVar_hsa_circ_75615,RMVar_hsa_circ_339453,RMVar_hsa_circ_307661,RMVar_hsa_circ_309835,RMVar_hsa_circ_47344,RMVar_hsa_circ_294609,RMVar_hsa_circ_36630,RMVar_hsa_circ_46957,RMVar_hsa_circ_82814,RMVar_hsa_circ_57238,RMVar_hsa_circ_118919,RMVar_hsa_circ_64453,RMVar_hsa_circ_242295,RMVar_hsa_circ_85300,RMVar_hsa_circ_242298,RMVar_hsa_circ_6300,RMVar_hsa_circ_242299,RMVar_hsa_circ_242301,RMVar_hsa_circ_17387,RMVar_hsa_circ_291513,RMVar_hsa_circ_343761,RMVar_hsa_circ_242302,RMVar_hsa_circ_242304,RMVar_hsa_circ_99529,RMVar_hsa_circ_99854,RMVar_hsa_circ_242305 44946 RMVar_ID_44946 Human_SNP_ID_301502045 A-to-I Human chr6 + 150946370 150946370 150946370 TGGGATTTCACCATGTTGGCCAGGCTGGTCTCAAACGCCTGACCTCAAGTGATCCATCCACCTTG TGGGATTTCACCATGTTGGCCAGGCTGGTCTCGAACGCCTGACCTCAAGTGATCCATCCACCTTG A G MTHFD1L Ensembl:ENSG00000120254 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs200337423 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_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_84744,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_280794,RMVar_hsa_circ_242315,RMVar_hsa_circ_242316,RMVar_hsa_circ_306737,RMVar_hsa_circ_311801,RMVar_hsa_circ_348341,RMVar_hsa_circ_288971,RMVar_hsa_circ_127783,RMVar_hsa_circ_86612,RMVar_hsa_circ_242317,RMVar_hsa_circ_242319,RMVar_hsa_circ_242321,RMVar_hsa_circ_21076,RMVar_hsa_circ_242322,RMVar_hsa_circ_242320,RMVar_hsa_circ_242318,RMVar_hsa_circ_242324,RMVar_hsa_circ_90387 44947 RMVar_ID_44947 Human_SNP_ID_301511402 A-to-I Human chr6 + 150984023 150984023 150984023 TAAACTCCTGAGCTCAAGTGATCGCCTGCCTCAGCCTCCCAAAATGCTGGGATTACAGGCATGAA TAAACTCCTGAGCTCAAGTGATCGCCTGCCTCGGCCTCCCAAAATGCTGGGATTACAGGCATGAA A G MTHFD1L Ensembl:ENSG00000120254 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1324688060 Functional Loss SNV dbSNP153 33..33 33 - - - 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_61258,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_6210,RMVar_hsa_circ_265387,RMVar_hsa_circ_348341,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 44948 RMVar_ID_44948 Human_SNP_ID_301529491 A-to-I Human chr6 + 151057979 151057979 151057979 TTTTGTATTTTTAGAAGAGACAGTTTCACCATATTGGCCAGACTGGTCTCAAACTCCTGACCGCA TTTTGTATTTTTAGAAGAGACAGTTTCACCATGTTGGCCAGACTGGTCTCAAACTCCTGACCGCA A G MTHFD1L Ensembl:ENSG00000120254 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs911479658 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111201,RMVar_hsa_circ_242306,RMVar_hsa_circ_242330,RMVar_hsa_circ_242324,RMVar_hsa_circ_90387,RMVar_hsa_circ_373401,RMVar_hsa_circ_67375,RMVar_hsa_circ_242335,RMVar_hsa_circ_377399,RMVar_hsa_circ_33387 44949 RMVar_ID_44949 Human_SNP_ID_301610066 A-to-I Human chr6 - 151368935 151368934 151368935 AACACAGTGAAATCCTGTCTCTACTAAAAAAAATACAAAAATTAGCTGGGCCTGGTGGCGGGCAC AACACAGTGAAATCCTGTCTCTACTAAAAAAA_TACAAAAATTAGCTGGGCCTGGTGGCGGGCAC AT A ZBTB2 Ensembl:ENSG00000181472 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs906635475 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_78269,RMVar_hsa_circ_242344 44950 RMVar_ID_44950 Human_SNP_ID_301610398 A-to-I Human chr6 - 151370292 151370292 151370292 ATCTCTACTAAAAATAGAAAAATTAGCCGGGCATCGTGGCGTGCACCTGTAATCCCAGCTACTCG ATCTCTACTAAAAATAGAAAAATTAGCCGGGCGTCGTGGCGTGCACCTGTAATCCCAGCTACTCG T C ZBTB2 Ensembl:ENSG00000181472 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs563656633 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78269,RMVar_hsa_circ_242344 44951 RMVar_ID_44951 Human_SNP_ID_301615163 A-to-I Human chr6 - 151388642 151388642 151388642 GTGTTCATGGCCAGGGAAAGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCCAAGGCTGGA GTGTTCATGGCCAGGGAAAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCTGGA T C ZBTB2 Ensembl:ENSG00000181472 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs986465762 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78269,RMVar_hsa_circ_242344 44952 RMVar_ID_44952 Human_SNP_ID_301617357 A-to-I Human chr6 + 151394028 151394028 151394028 AAAGAATTAGCCAGGCGTGATGGTGTGGGTCTATAGTCTCAGCTTGGGAGGCTGAGGTGGCAGGA AAAGAATTAGCCAGGCGTGATGGTGTGGGTCTCTAGTCTCAGCTTGGGAGGCTGAGGTGGCAGGA A C lnc-AKAP12-1,lnc-AKAP12-1:2 RNACentral:URS00008C063A,RNACentral:URS00008C2BAE lincRNA,lincRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1135310 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15690472,Human_RBP_ID_25975806 44953 RMVar_ID_44953 Human_SNP_ID_301617358 A-to-I Human chr6 + 151394028 151394028 151394028 AAAGAATTAGCCAGGCGTGATGGTGTGGGTCTATAGTCTCAGCTTGGGAGGCTGAGGTGGCAGGA AAAGAATTAGCCAGGCGTGATGGTGTGGGTCTGTAGTCTCAGCTTGGGAGGCTGAGGTGGCAGGA A G lnc-AKAP12-1,lnc-AKAP12-1:2 RNACentral:URS00008C063A,RNACentral:URS00008C2BAE lincRNA,lincRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1135310 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15690472,Human_RBP_ID_25975806 44954 RMVar_ID_44954 Human_SNP_ID_301619201 A-to-I Human chr6 + 151400434 151400434 151400434 ATGCCAGCGCACCTGGCTAATTTAGTATTTTTAGTAGAGACGGGGTTTCTCCATGTTGGTCAGGC ATGCCAGCGCACCTGGCTAATTTAGTATTTTTGGTAGAGACGGGGTTTCTCCATGTTGGTCAGGC A G lnc-AKAP12-1 RNACentral:URS00008C2BAE lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1016543370 Functional Loss SNV dbSNP153 33..33 33 - - - 44955 RMVar_ID_44955 Human_SNP_ID_301619206 A-to-I Human chr6 + 151400454 151400454 151400454 TTTAGTATTTTTAGTAGAGACGGGGTTTCTCCATGTTGGTCAGGCTGGTCTCAATTTCCGGACCT TTTAGTATTTTTAGTAGAGACGGGGTTTCTCCGTGTTGGTCAGGCTGGTCTCAATTTCCGGACCT A G lnc-AKAP12-1 RNACentral:URS00008C2BAE lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1278855265 Functional Loss SNV dbSNP153 33..33 33 - - - 44956 RMVar_ID_44956 Human_SNP_ID_301620634 A-to-I Human chr6 - 151404997 151404992 151404997 AGGTGTGTTGGCACACGCCCGTCATCTCAGCTACTCAGGAGGCTGAGGCAGGAGAATCTCTTGAA AGGTGTGTTGGCACACGCCCGTCATCTCAGCT_____GGAGGCTGAGGCAGGAGAATCTCTTGAA CTGAGT C RMND1 Ensembl:ENSG00000155906 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1166490253 Functional Loss DEL dbSNP153 33..37 33 - - - RMVar_hsa_circ_242346 44957 RMVar_ID_44957 Human_SNP_ID_301621592 A-to-I Human chr6 - 151407768 151407768 151407768 TGACTGGCTGGGACAACAGGGGCCGCCACAACACCCGGATAATTTTTTTGTATTTTTAGTAGAGA TGACTGGCTGGGACAACAGGGGCCGCCACAACCCCCGGATAATTTTTTTGTATTTTTAGTAGAGA T G RMND1 Ensembl:ENSG00000155906 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs894191046 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63798,RMVar_hsa_circ_242346,RMVar_hsa_circ_311981,RMVar_hsa_circ_67318,RMVar_hsa_circ_242347,RMVar_hsa_circ_242348 44958 RMVar_ID_44958 Human_SNP_ID_301621612 A-to-I Human chr6 - 151407823 151407823 151407823 CACTGCAAGCTCCACCTCCCGGCTGGGTTCACACTATTCTCCTGCCTCAGCCTCCTGACTGGCTG CACTGCAAGCTCCACCTCCCGGCTGGGTTCACGCTATTCTCCTGCCTCAGCCTCCTGACTGGCTG T C RMND1 Ensembl:ENSG00000155906 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1197694498 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63798,RMVar_hsa_circ_242346,RMVar_hsa_circ_311981,RMVar_hsa_circ_67318,RMVar_hsa_circ_242347,RMVar_hsa_circ_242348 44959 RMVar_ID_44959 Human_SNP_ID_301623981 A-to-I Human chr6 - 151416175 151416175 151416175 CAAGAGTTCGAGACCTGCCTGGCCAATATGGTAAAACGCTGTCTCTACTAAAAATACAAAAATTA CAAGAGTTCGAGACCTGCCTGGCCAATATGGTGAAACGCTGTCTCTACTAAAAATACAAAAATTA T C RMND1 Ensembl:ENSG00000155906 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1246316088 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63798,RMVar_hsa_circ_242346,RMVar_hsa_circ_311981,RMVar_hsa_circ_67318,RMVar_hsa_circ_242347,RMVar_hsa_circ_242348 44960 RMVar_ID_44960 Human_SNP_ID_301624537 A-to-I Human chr6 - 151418242 151418242 151418242 ACCTGGCTAGTTCTTGTATTTTTTGTAGAGATAGGGTTTCGCTGTGCTGTCCAGGTTGGTCTTGA ACCTGGCTAGTTCTTGTATTTTTTGTAGAGATGGGGTTTCGCTGTGCTGTCCAGGTTGGTCTTGA T C RMND1 Ensembl:ENSG00000155906 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1048914764 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17576512 RMVar_hsa_circ_63798,RMVar_hsa_circ_242346,RMVar_hsa_circ_311981,RMVar_hsa_circ_67318,RMVar_hsa_circ_242352,RMVar_hsa_circ_320868,RMVar_hsa_circ_242347,RMVar_hsa_circ_242348,RMVar_hsa_circ_321765,RMVar_hsa_circ_361421,RMVar_hsa_circ_282114,RMVar_hsa_circ_307528,RMVar_hsa_circ_106003,RMVar_hsa_circ_242350,RMVar_hsa_circ_242351,RMVar_hsa_circ_242349 44961 RMVar_ID_44961 Human_SNP_ID_301628803 A-to-I Human chr6 - 151435254 151435254 151435254 GTAGTCCCAGCTACTTGGGAGACTGAGACACAAGAATTGCTTGAACCTGGAGGGTGGAGGTTGCA GTAGTCCCAGCTACTTGGGAGACTGAGACACACGAATTGCTTGAACCTGGAGGGTGGAGGTTGCA T G RMND1 Ensembl:ENSG00000155906 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs535988262 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42460,RMVar_hsa_circ_111862,RMVar_hsa_circ_242352,RMVar_hsa_circ_361421,RMVar_hsa_circ_307528,RMVar_hsa_circ_37235,RMVar_hsa_circ_242354,RMVar_hsa_circ_62098,RMVar_hsa_circ_52559,RMVar_hsa_circ_361573,RMVar_hsa_circ_343837,RMVar_hsa_circ_242357 44962 RMVar_ID_44962 Human_SNP_ID_301693650 A-to-I Human chr6 + 151694610 151694610 151694610 AAGAGTTCGTGACCAGCCTGGCCAACACGGTGAAACCCGTCTCCACTAAAAATACAAAAATTAGC AAGAGTTCGTGACCAGCCTGGCCAACACGGTGGAACCCGTCTCCACTAAAAATACAAAAATTAGC A G ESR1 Ensembl:ENSG00000091831 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs888714334 Functional Loss SNV dbSNP153 33..33 33 - - - 44963 RMVar_ID_44963 Human_SNP_ID_301825625 A-to-I Human chr6 - 152252077 152252077 152252077 AGTAGAGATGGGCTTTCACTGTATGTTGGCCAAGCTGGTCTCGAACTCCCGACCTCAGGTCATCT AGTAGAGATGGGCTTTCACTGTATGTTGGCCAGGCTGGTCTCGAACTCCCGACCTCAGGTCATCT T C SYNE1 Ensembl:ENSG00000131018 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs968093494 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81907,RMVar_hsa_circ_242364,RMVar_hsa_circ_242365,RMVar_hsa_circ_83733,RMVar_hsa_circ_10051,RMVar_hsa_circ_85706,RMVar_hsa_circ_242368,RMVar_hsa_circ_49492,RMVar_hsa_circ_44672,RMVar_hsa_circ_33861,RMVar_hsa_circ_93742,RMVar_hsa_circ_269308,RMVar_hsa_circ_242371,RMVar_hsa_circ_71908,RMVar_hsa_circ_242372,RMVar_hsa_circ_42865,RMVar_hsa_circ_127654,RMVar_hsa_circ_242374,RMVar_hsa_circ_23872,RMVar_hsa_circ_11624,RMVar_hsa_circ_334000,RMVar_hsa_circ_267727,RMVar_hsa_circ_242380,RMVar_hsa_circ_301954,RMVar_hsa_circ_118186,RMVar_hsa_circ_57458,RMVar_hsa_circ_365365,RMVar_hsa_circ_242384,RMVar_hsa_circ_351360,RMVar_hsa_circ_365574,RMVar_hsa_circ_300778,RMVar_hsa_circ_242386,RMVar_hsa_circ_309163,RMVar_hsa_circ_242389,RMVar_hsa_circ_12514,RMVar_hsa_circ_22749,RMVar_hsa_circ_242387,RMVar_hsa_circ_276283,RMVar_hsa_circ_342995,RMVar_hsa_circ_56364,RMVar_hsa_circ_242388 44964 RMVar_ID_44964 Human_SNP_ID_301831233 A-to-I Human chr6 - 152274804 152274804 152274804 ATCACCTGAGGTCAGGAGTTCGAGACCAGCCTAGCCAACATAGTGAAACTCCGTCTATACTAAAA ATCACCTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATAGTGAAACTCCGTCTATACTAAAA T C SYNE1 Ensembl:ENSG00000131018 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1562696245 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_242365,RMVar_hsa_circ_83733,RMVar_hsa_circ_85706,RMVar_hsa_circ_242368,RMVar_hsa_circ_49492,RMVar_hsa_circ_44672,RMVar_hsa_circ_93742,RMVar_hsa_circ_242372,RMVar_hsa_circ_8507,RMVar_hsa_circ_267727,RMVar_hsa_circ_57458,RMVar_hsa_circ_242389,RMVar_hsa_circ_22749,RMVar_hsa_circ_342995,RMVar_hsa_circ_322937,RMVar_hsa_circ_369859,RMVar_hsa_circ_242391,RMVar_hsa_circ_9239 44965 RMVar_ID_44965 Human_SNP_ID_301831420 A-to-I Human chr6 - 152275658 152275658 152275658 CCAGGCTGGTCTTCAACTCCTGAGCACAGGCAATCCACCCACCTCAGCCTCCCAAAGTGCTGAGA CCAGGCTGGTCTTCAACTCCTGAGCACAGGCAGTCCACCCACCTCAGCCTCCCAAAGTGCTGAGA T C SYNE1 Ensembl:ENSG00000131018 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs771728765 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_242365,RMVar_hsa_circ_83733,RMVar_hsa_circ_85706,RMVar_hsa_circ_242368,RMVar_hsa_circ_49492,RMVar_hsa_circ_44672,RMVar_hsa_circ_93742,RMVar_hsa_circ_242372,RMVar_hsa_circ_8507,RMVar_hsa_circ_267727,RMVar_hsa_circ_57458,RMVar_hsa_circ_242389,RMVar_hsa_circ_22749,RMVar_hsa_circ_342995,RMVar_hsa_circ_322937,RMVar_hsa_circ_369859,RMVar_hsa_circ_242391,RMVar_hsa_circ_9239 44966 RMVar_ID_44966 Human_SNP_ID_301841438 A-to-I Human chr6 - 152315415 152315415 152315415 TGGGTGGATCACAAGGTCAGGAGTTCAAGACCAGCTTGGCCAATATGGTGAAACCCCATCTCTAC TGGGTGGATCACAAGGTCAGGAGTTCAAGACCCGCTTGGCCAATATGGTGAAACCCCATCTCTAC T G SYNE1 Ensembl:ENSG00000131018 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1376224118 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85706,RMVar_hsa_circ_242368,RMVar_hsa_circ_93742,RMVar_hsa_circ_242372,RMVar_hsa_circ_94707,RMVar_hsa_circ_291845,RMVar_hsa_circ_113734,RMVar_hsa_circ_124484,RMVar_hsa_circ_242394,RMVar_hsa_circ_242395,RMVar_hsa_circ_352953,RMVar_hsa_circ_242393,RMVar_hsa_circ_340289,RMVar_hsa_circ_242399,RMVar_hsa_circ_47333,RMVar_hsa_circ_242398,RMVar_hsa_circ_323873,RMVar_hsa_circ_242402,RMVar_hsa_circ_2622 44967 RMVar_ID_44967 Human_SNP_ID_301857749 A-to-I Human chr6 - 152374691 152374691 152374691 TGGTTCACTGCAACCTCTGCCTCCCACGTTCAAGCAATCCTCCTGCCTCAGCCTCCTGAGTATCT TGGTTCACTGCAACCTCTGCCTCCCACGTTCAGGCAATCCTCCTGCCTCAGCCTCCTGAGTATCT T C SYNE1 Ensembl:ENSG00000131018 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1245327173 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94707,RMVar_hsa_circ_113734,RMVar_hsa_circ_124484,RMVar_hsa_circ_242394,RMVar_hsa_circ_242393,RMVar_hsa_circ_242399,RMVar_hsa_circ_102691,RMVar_hsa_circ_269288,RMVar_hsa_circ_242410,RMVar_hsa_circ_79057,RMVar_hsa_circ_242409,RMVar_hsa_circ_8980,RMVar_hsa_circ_58196 44968 RMVar_ID_44968 Human_SNP_ID_301897465 A-to-I Human chr6 - 152533902 152533902 152533902 CACCAACCTCAGCCTCCCAAAATGCTGGGATTACAGCTGTAAGCCACCGTGCCCAACCAGAAATA CACCAACCTCAGCCTCCCAAAATGCTGGGATTGCAGCTGTAAGCCACCGTGCCCAACCAGAAATA T C SYNE1 Ensembl:ENSG00000131018 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1383298900 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_242410,RMVar_hsa_circ_79057,RMVar_hsa_circ_116490,RMVar_hsa_circ_242424,RMVar_hsa_circ_242423,RMVar_hsa_circ_279604 44969 RMVar_ID_44969 Human_SNP_ID_302009202 A-to-I Human chr6 - 152986256 152986256 152986256 GTCGCCAGGCTGGAGTGCAGTGATGCGATCTCAGCTCACTGCAACCTCTGCCTCTGGGCTCAAGC GTCGCCAGGCTGGAGTGCAGTGATGCGATCTCTGCTCACTGCAACCTCTGCCTCTGGGCTCAAGC T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs899808271 Functional Loss SNV dbSNP153 33..33 33 - - - 44970 RMVar_ID_44970 Human_SNP_ID_302009332 A-to-I Human chr6 + 152986734 152986734 152986734 CACTTGGAAGGCCTAGGTGGGCAGATCACCTGAGGTCAGAAGTTCAAGACCAGCCTGGCCAACAT CACTTGGAAGGCCTAGGTGGGCAGATCACCTGTGGTCAGAAGTTCAAGACCAGCCTGGCCAACAT A T AL080276.2 Ensembl:ENSG00000227627 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs951495363 Functional Loss SNV dbSNP153 33..33 33 - - - 44971 RMVar_ID_44971 Human_SNP_ID_302377513 A-to-I Human chr6 - 154489334 154489334 154489334 TCGAGATGTGGTTTCACCGTGTTACCAAGACTAGTCTTGAACTCCTGACCTCAAGTGATCTGCCC TCGAGATGTGGTTTCACCGTGTTACCAAGACTGGTCTTGAACTCCTGACCTCAAGTGATCTGCCC T C AL357075.4,CNKSR3 Ensembl:ENSG00000288520,Ensembl:ENSG00000153721 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1397239250 Functional Loss SNV dbSNP153 33..33 33 - - - 44972 RMVar_ID_44972 Human_SNP_ID_302440485 A-to-I Human chr6 + 154735613 154735613 154735613 TCAGCTCACTGTAGCCTCCACCTCCCGGTTTCAAGCGATTCTTCTGCCTCAGTGTCCCGAGTAGC TCAGCTCACTGTAGCCTCCACCTCCCGGTTTCTAGCGATTCTTCTGCCTCAGTGTCCCGAGTAGC A T SCAF8 Ensembl:ENSG00000213079 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1306985378 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15695277 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_242465 44973 RMVar_ID_44973 Human_SNP_ID_302452264 A-to-I Human chr6 + 154778684 154778684 154778684 TACTTGGGAGGCTGAGGCACAAGAATTGCTTGAACCCAGGGGGCGGAGGTTGTAGTGAGCTGAGA TACTTGGGAGGCTGAGGCACAAGAATTGCTTGTACCCAGGGGGCGGAGGTTGTAGTGAGCTGAGA A T SCAF8 Ensembl:ENSG00000213079 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1463822784 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25977279 RMVar_hsa_circ_31352,RMVar_hsa_circ_314911,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_242465,RMVar_hsa_circ_108288,RMVar_hsa_circ_345398,RMVar_hsa_circ_242467,RMVar_hsa_circ_98611,RMVar_hsa_circ_242468,RMVar_hsa_circ_373198,RMVar_hsa_circ_376513,RMVar_hsa_circ_242466,RMVar_hsa_circ_375447,RMVar_hsa_circ_325434,RMVar_hsa_circ_341708,RMVar_hsa_circ_322232,RMVar_hsa_circ_288812,RMVar_hsa_circ_294605,RMVar_hsa_circ_285348,RMVar_hsa_circ_80325,RMVar_hsa_circ_270915,RMVar_hsa_circ_55800,RMVar_hsa_circ_242476,RMVar_hsa_circ_242480,RMVar_hsa_circ_242484,RMVar_hsa_circ_242486,RMVar_hsa_circ_242485,RMVar_hsa_circ_242482,RMVar_hsa_circ_242483,RMVar_hsa_circ_242481,RMVar_hsa_circ_242478,RMVar_hsa_circ_242479,RMVar_hsa_circ_242477,RMVar_hsa_circ_242472,RMVar_hsa_circ_242474,RMVar_hsa_circ_242475,RMVar_hsa_circ_242473,RMVar_hsa_circ_242489,RMVar_hsa_circ_354354,RMVar_hsa_circ_242470,RMVar_hsa_circ_242471,RMVar_hsa_circ_360990,RMVar_hsa_circ_369853,RMVar_hsa_circ_242491,RMVar_hsa_circ_280415,RMVar_hsa_circ_242490 44974 RMVar_ID_44974 Human_SNP_ID_302456642 A-to-I Human chr6 + 154793668 154793668 154793668 GAAACCCTGTCTACATTAAAAATAAAAAAATCAGCTGGGTGTGGTAGTGGGTGCCTGTAATCCCA GAAACCCTGTCTACATTAAAAATAAAAAAATCGGCTGGGTGTGGTAGTGGGTGCCTGTAATCCCA A G SCAF8 Ensembl:ENSG00000213079 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1191942374 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_31352,RMVar_hsa_circ_314911,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_242465,RMVar_hsa_circ_108288,RMVar_hsa_circ_345398,RMVar_hsa_circ_242467,RMVar_hsa_circ_98611,RMVar_hsa_circ_242468,RMVar_hsa_circ_373198,RMVar_hsa_circ_376513,RMVar_hsa_circ_242466,RMVar_hsa_circ_375447,RMVar_hsa_circ_325434,RMVar_hsa_circ_341708,RMVar_hsa_circ_322232,RMVar_hsa_circ_294605,RMVar_hsa_circ_80325,RMVar_hsa_circ_270915,RMVar_hsa_circ_55800,RMVar_hsa_circ_70538,RMVar_hsa_circ_242476,RMVar_hsa_circ_242480,RMVar_hsa_circ_242484,RMVar_hsa_circ_242482,RMVar_hsa_circ_242483,RMVar_hsa_circ_242481,RMVar_hsa_circ_242478,RMVar_hsa_circ_242479,RMVar_hsa_circ_242477,RMVar_hsa_circ_242472,RMVar_hsa_circ_242474,RMVar_hsa_circ_242475,RMVar_hsa_circ_242473,RMVar_hsa_circ_242489,RMVar_hsa_circ_354354,RMVar_hsa_circ_242470,RMVar_hsa_circ_242471,RMVar_hsa_circ_369853,RMVar_hsa_circ_242490,RMVar_hsa_circ_303630,RMVar_hsa_circ_373953,RMVar_hsa_circ_322469,RMVar_hsa_circ_293441,RMVar_hsa_circ_268484,RMVar_hsa_circ_274588,RMVar_hsa_circ_126668,RMVar_hsa_circ_242494,RMVar_hsa_circ_242496,RMVar_hsa_circ_242498,RMVar_hsa_circ_242499,RMVar_hsa_circ_242497,RMVar_hsa_circ_242495,RMVar_hsa_circ_54255,RMVar_hsa_circ_75463,RMVar_hsa_circ_333646 44975 RMVar_ID_44975 Human_SNP_ID_302500689 A-to-I Human chr6 + 154962618 154962618 154962618 TTGGGAGGTGGAGGTTGCAGTGAGCCGAGATGAAGCCATTGCACTCCAGCTTGGGCAACACAGCA TTGGGAGGTGGAGGTTGCAGTGAGCCGAGATGGAGCCATTGCACTCCAGCTTGGGCAACACAGCA A G TIAM2 Ensembl:ENSG00000146426 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1449271632 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125833,RMVar_hsa_circ_242513 44976 RMVar_ID_44976 Human_SNP_ID_302500918 A-to-I Human chr6 + 154963779 154963779 154963779 GCCACCACACCCAGATAATTTTTTGTATTTTTAGTAGAGAGAGAGTTTCACTGTGTTAGCCAGTA GCCACCACACCCAGATAATTTTTTGTATTTTTCGTAGAGAGAGAGTTTCACTGTGTTAGCCAGTA A C TIAM2 Ensembl:ENSG00000146426 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1304289917 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125833,RMVar_hsa_circ_242513 44977 RMVar_ID_44977 Human_SNP_ID_302968898 A-to-I Human chr6 + 156835842 156835842 156835842 TGGCTCACTGCGGCCTTGACCTCCTGGGCTCAAACAATCCTCCCACCTCAGCCTCCCAAGCAGTT TGGCTCACTGCGGCCTTGACCTCCTGGGCTCACACAATCCTCCCACCTCAGCCTCCCAAGCAGTT A C ARID1B Ensembl:ENSG00000049618 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1302820966 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_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_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 44978 RMVar_ID_44978 Human_SNP_ID_302968899 A-to-I Human chr6 + 156835842 156835842 156835842 TGGCTCACTGCGGCCTTGACCTCCTGGGCTCAAACAATCCTCCCACCTCAGCCTCCCAAGCAGTT TGGCTCACTGCGGCCTTGACCTCCTGGGCTCAGACAATCCTCCCACCTCAGCCTCCCAAGCAGTT A G ARID1B Ensembl:ENSG00000049618 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1302820966 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_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_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 44979 RMVar_ID_44979 Human_SNP_ID_302968901 A-to-I Human chr6 + 156835854 156835854 156835854 GCCTTGACCTCCTGGGCTCAAACAATCCTCCCACCTCAGCCTCCCAAGCAGTTGGGACTACAGAC GCCTTGACCTCCTGGGCTCAAACAATCCTCCCTCCTCAGCCTCCCAAGCAGTTGGGACTACAGAC A T ARID1B Ensembl:ENSG00000049618 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs948409832 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_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_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 44980 RMVar_ID_44980 Human_SNP_ID_302974449 A-to-I Human chr6 + 156858675 156858675 156858675 CCTGTAGTTCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGGACCCAGAAGGTGGTGGCT CCTGTAGTTCCAGCTACTCAGGAGGCTGAGGCGGGAGAATCGCTTGGACCCAGAAGGTGGTGGCT A G ARID1B Ensembl:ENSG00000049618 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1014567595 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_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 44981 RMVar_ID_44981 Human_SNP_ID_302997503 A-to-I Human chr6 + 156948342 156948342 156948342 TAGACTCAGCCTCCCACCTCAGCCTCTCGAGTAGCTGGAACTATAGGCGTGTGCCACCACGCCTG TAGACTCAGCCTCCCACCTCAGCCTCTCGAGTGGCTGGAACTATAGGCGTGTGCCACCACGCCTG A G ARID1B Ensembl:ENSG00000049618 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559956784 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_366641,RMVar_hsa_circ_360725,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_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_242567,RMVar_hsa_circ_341282,RMVar_hsa_circ_125504,RMVar_hsa_circ_242570,RMVar_hsa_circ_100236,RMVar_hsa_circ_102259,RMVar_hsa_circ_96438,RMVar_hsa_circ_242572,RMVar_hsa_circ_242573,RMVar_hsa_circ_242571,RMVar_hsa_circ_242568,RMVar_hsa_circ_242569 44982 RMVar_ID_44982 Human_SNP_ID_303006372 A-to-I Human chr6 + 156984800 156984800 156984800 CCTCAACCTCCCTGGGCTCAGGTGATCCTCCCACCTCAGCCTCATGAGTAGTTGGGACTACGGGC CCTCAACCTCCCTGGGCTCAGGTGATCCTCCCGCCTCAGCCTCATGAGTAGTTGGGACTACGGGC A G ARID1B Ensembl:ENSG00000049618 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs912280575 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_827198 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_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_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_242567,RMVar_hsa_circ_341282,RMVar_hsa_circ_125504,RMVar_hsa_circ_242570,RMVar_hsa_circ_100236,RMVar_hsa_circ_102259,RMVar_hsa_circ_96438,RMVar_hsa_circ_242572,RMVar_hsa_circ_242573,RMVar_hsa_circ_242571,RMVar_hsa_circ_242577,RMVar_hsa_circ_242568,RMVar_hsa_circ_242569 44983 RMVar_ID_44983 Human_SNP_ID_303007810 A-to-I Human chr6 + 156990381 156990381 156990381 ACAGCTTTTGTAGGCCGGGCGCTGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGC ACAGCTTTTGTAGGCCGGGCGCTGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGC A G ARID1B Ensembl:ENSG00000049618 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs987182076 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21948376 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_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_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_242567,RMVar_hsa_circ_341282,RMVar_hsa_circ_125504,RMVar_hsa_circ_242570,RMVar_hsa_circ_100236,RMVar_hsa_circ_102259,RMVar_hsa_circ_96438,RMVar_hsa_circ_242572,RMVar_hsa_circ_242573,RMVar_hsa_circ_242571,RMVar_hsa_circ_242577,RMVar_hsa_circ_242568,RMVar_hsa_circ_242569 44984 RMVar_ID_44984 Human_SNP_ID_303014567 A-to-I Human chr6 + 157018011 157018011 157018011 AAAATTAGCTGGGCATGGTGTCATGTGCTTGTAGTCCCAGTTACTCAAGGGGCTAAGGTGGGAGG AAAATTAGCTGGGCATGGTGTCATGTGCTTGTGGTCCCAGTTACTCAAGGGGCTAAGGTGGGAGG A G ARID1B Ensembl:ENSG00000049618 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1211279953 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_366641,RMVar_hsa_circ_360725,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_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_242567,RMVar_hsa_circ_341282,RMVar_hsa_circ_125504,RMVar_hsa_circ_242570,RMVar_hsa_circ_100236,RMVar_hsa_circ_102259,RMVar_hsa_circ_96438,RMVar_hsa_circ_242572,RMVar_hsa_circ_242573,RMVar_hsa_circ_242571,RMVar_hsa_circ_242577,RMVar_hsa_circ_242568,RMVar_hsa_circ_242569 44985 RMVar_ID_44985 Human_SNP_ID_303016657 A-to-I Human chr6 + 157024678 157024678 157024678 CCTGTAATCCCAGCTACTCAGGTGGCTGAGGCAGGGAAATCACTTGAACCTGGAGGCAGAGGTTA CCTGTAATCCCAGCTACTCAGGTGGCTGAGGCGGGGAAATCACTTGAACCTGGAGGCAGAGGTTA A G ARID1B Ensembl:ENSG00000049618 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs931711412 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_366641,RMVar_hsa_circ_360725,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_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_242567,RMVar_hsa_circ_341282,RMVar_hsa_circ_125504,RMVar_hsa_circ_242570,RMVar_hsa_circ_100236,RMVar_hsa_circ_102259,RMVar_hsa_circ_96438,RMVar_hsa_circ_242572,RMVar_hsa_circ_242573,RMVar_hsa_circ_242571,RMVar_hsa_circ_242577,RMVar_hsa_circ_242568,RMVar_hsa_circ_242569 44986 RMVar_ID_44986 Human_SNP_ID_303045165 A-to-I Human chr6 + 157139924 157139924 157139924 TTTCATATTTTTAGTAGAGGCAGGTTTTCACCATGTTGGCCAAGCTGGCCTCAAATTCCTGACCT TTTCATATTTTTAGTAGAGGCAGGTTTTCACCGTGTTGGCCAAGCTGGCCTCAAATTCCTGACCT A G ARID1B Ensembl:ENSG00000049618 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1190080384 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_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_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_305696,RMVar_hsa_circ_103831,RMVar_hsa_circ_124768,RMVar_hsa_circ_299017,RMVar_hsa_circ_242582,RMVar_hsa_circ_277083,RMVar_hsa_circ_242585,RMVar_hsa_circ_105739,RMVar_hsa_circ_124135,RMVar_hsa_circ_242587,RMVar_hsa_circ_242586,RMVar_hsa_circ_242583,RMVar_hsa_circ_242584,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_89886,RMVar_hsa_circ_352333,RMVar_hsa_circ_242597,RMVar_hsa_circ_242598 44987 RMVar_ID_44987 Human_SNP_ID_303104444 A-to-I Human chr6 - 157366464 157366464 157366464 AATACTTTTTGGACATTCCTGACTTGGACAATATGATCAAGAAAATGATAAATATTAATATTCTC AATACTTTTTGGACATTCCTGACTTGGACAATGTGATCAAGAAAATGATAAATATTAATATTCTC T C AL390955.1 Ensembl:ENSG00000213078 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1336214832 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22404929 44988 RMVar_ID_44988 Human_SNP_ID_303104457 A-to-I Human chr6 - 157366510 157366510 157366510 ATCGGCGTCTTAGTGAACAACGTGGGAATGTCATATGAGTATCCCAAATACTTTTTGGACATTCC ATCGGCGTCTTAGTGAACAACGTGGGAATGTCGTATGAGTATCCCAAATACTTTTTGGACATTCC T C AL390955.1 Ensembl:ENSG00000213078 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1436673537 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26533288 44989 RMVar_ID_44989 Human_SNP_ID_303177970 A-to-I Human chr6 + 157670394 157670394 157670394 CAGCTCACTGGAACCTCTGCCTTCTGGGCTCAAATGATTCTCCTACCTCAGCCTCCTGAGAAGCT CAGCTCACTGGAACCTCTGCCTTCTGGGCTCAGATGATTCTCCTACCTCAGCCTCCTGAGAAGCT A G ZDHHC14 Ensembl:ENSG00000175048 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs762102593 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8635315 RMVar_hsa_circ_118931,RMVar_hsa_circ_242613,RMVar_hsa_circ_105864,RMVar_hsa_circ_242616,RMVar_hsa_circ_107660,RMVar_hsa_circ_86761,RMVar_hsa_circ_242617,RMVar_hsa_circ_242618 44990 RMVar_ID_44990 Human_SNP_ID_303288543 A-to-I Human chr6 - 158113545 158113545 158113545 AAACACTACAAGATGACTTTCTGGAGTTTGCTAAAGACAAAAACTTCCAGGTGCTGAATTTTGTG AAACACTACAAGATGACTTTCTGGAGTTTGCTGAAGACAAAAACTTCCAGGTGCTGAATTTTGTG T C SERAC1 Ensembl:ENSG00000122335 Protein coding CDS GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1268234019 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_827910,Human_Splice_Rec_827911,Human_Splice_Rec_827946,Human_Splice_Rec_827947,Human_Splice_Rec_827972,Human_Splice_Rec_827973,Human_Splice_Rec_828000,Human_Splice_Rec_828001,Human_Splice_Rec_828028,Human_Splice_Rec_828029,Human_Splice_Rec_828056,Human_Splice_Rec_828082,Human_Splice_Rec_828083,Human_Splice_Rec_828112,Human_Splice_Rec_828113,Human_Splice_Rec_828146,Human_Splice_Rec_828147,Human_Splice_Rec_828174,Human_Splice_Rec_828175,Human_Splice_Rec_828206 RMVar_hsa_circ_13580,RMVar_hsa_circ_49373,RMVar_hsa_circ_242649,RMVar_hsa_circ_266090,RMVar_hsa_circ_340353,RMVar_hsa_circ_48839,RMVar_hsa_circ_242650,RMVar_hsa_circ_242651 44991 RMVar_ID_44991 Human_SNP_ID_303310122 A-to-I Human chr6 + 158198488 158198488 158198488 AAGATCTCGCTCTGTTGCTCAGGCTGAAGTGCAATAGCGCAAACTCGGCTCACTGCAACCTCCCA AAGATCTCGCTCTGTTGCTCAGGCTGAAGTGCGATAGCGCAAACTCGGCTCACTGCAACCTCCCA A G GTF2H5 Ensembl:ENSG00000272047 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1288634889 Functional Loss SNV dbSNP153 33..33 33 - - - 44992 RMVar_ID_44992 Human_SNP_ID_303310132 A-to-I Human chr6 + 158198520 158198520 158198520 AATAGCGCAAACTCGGCTCACTGCAACCTCCCAGGTTCAAGCAATTCTCGTGCCTCAGCCATCCC AATAGCGCAAACTCGGCTCACTGCAACCTCCCGGGTTCAAGCAATTCTCGTGCCTCAGCCATCCC A G GTF2H5 Ensembl:ENSG00000272047 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1304899544 Functional Loss SNV dbSNP153 33..33 33 - - - 44993 RMVar_ID_44993 Human_SNP_ID_303320674 A-to-I Human chr6 + 158235537 158235537 158235537 ATCCTTTTGTTCTTGCTGTTGTTTCTAGAGACAAGGTCTCACTATGTTGCCCAGGCTGGTCTTGA ATCCTTTTGTTCTTGCTGTTGTTTCTAGAGACGAGGTCTCACTATGTTGCCCAGGCTGGTCTTGA A G TULP4 Ensembl:ENSG00000130338 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1009357857 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18857493 44994 RMVar_ID_44994 Human_SNP_ID_303323223 A-to-I Human chr6 - 158242179 158242179 158242179 TTGCCACCATTCATTATCAGAAGACACTGATGAGACTGAGGAAGACCCACAGGCAGGACTGGCCA TTGCCACCATTCATTATCAGAAGACACTGATGGGACTGAGGAAGACCCACAGGCAGGACTGGCCA T C SRP72P2 Ensembl:ENSG00000188451 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1477497660 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17422759 44995 RMVar_ID_44995 Human_SNP_ID_303323232 A-to-I Human chr6 - 158242203 158242203 158242203 CATCCTACAAAAAGCTGAAGGTCTTTGCCACCATTCATTATCAGAAGACACTGATGAGACTGAGG CATCCTACAAAAAGCTGAAGGTCTTTGCCACCGTTCATTATCAGAAGACACTGATGAGACTGAGG T C SRP72P2 Ensembl:ENSG00000188451 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1458866291 Functional Loss SNV dbSNP153 33..33 33 - - - 44996 RMVar_ID_44996 Human_SNP_ID_303323235 A-to-I Human chr6 - 158242206 158242206 158242206 GAACATCCTACAAAAAGCTGAAGGTCTTTGCCACCATTCATTATCAGAAGACACTGATGAGACTG GAACATCCTACAAAAAGCTGAAGGTCTTTGCCGCCATTCATTATCAGAAGACACTGATGAGACTG T C SRP72P2 Ensembl:ENSG00000188451 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1336829763 Functional Loss SNV dbSNP153 33..33 33 - - - 44997 RMVar_ID_44997 Human_SNP_ID_303330559 A-to-I Human chr6 + 158271029 158271029 158271029 AAAATTACCCAGGCATGGTGGCAGGTGCCTATAATCCCAGATACATGGGAGGCTGAGGCAGGAGA AAAATTACCCAGGCATGGTGGCAGGTGCCTATGATCCCAGATACATGGGAGGCTGAGGCAGGAGA A G TULP4 Ensembl:ENSG00000130338 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1267959389 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_242667,RMVar_hsa_circ_242666,RMVar_hsa_circ_242665 44998 RMVar_ID_44998 Human_SNP_ID_303339544 A-to-I Human chr6 + 158306824 158306824 158306824 GGTGGATCACTTGAGCCTCGGAGTTCGAGACCAGCCTGGCTAACGTGGCGAAACCCTGTCTCTAC GGTGGATCACTTGAGCCTCGGAGTTCGAGACCCGCCTGGCTAACGTGGCGAAACCCTGTCTCTAC A C AL360169.2,TULP4 Ensembl:ENSG00000274023,Ensembl:ENSG00000130338 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1554278628 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_242667,RMVar_hsa_circ_242666,RMVar_hsa_circ_242669,RMVar_hsa_circ_242670,RMVar_hsa_circ_242673,RMVar_hsa_circ_242672 44999 RMVar_ID_44999 Human_SNP_ID_303353083 A-to-I Human chr6 + 158355139 158355139 158355139 TGTCACCTAGACTGGAGTACAGTGGCACAGTTATAGCTCACTGTAACCTAGAACTCCTGGGCCCA TGTCACCTAGACTGGAGTACAGTGGCACAGTTGTAGCTCACTGTAACCTAGAACTCCTGGGCCCA A G AL360169.2,TULP4 Ensembl:ENSG00000274023,Ensembl:ENSG00000130338 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1282807414 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101982,RMVar_hsa_circ_242676 45000 RMVar_ID_45000 Human_SNP_ID_303387338 A-to-I Human chr6 + 158490186 158490185 158490187 TTGGGCGGCCGAGGCGGGTGGATCACGAAGTCAAGAGATCTGGACCATCCTGGTCAACATGGTGA TTGGGCGGCCGAGGCGGGTGGATCACGAAGTC__GAGATCTGGACCATCCTGGTCAACATGGTGA CAA C TULP4 Ensembl:ENSG00000130338 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170963184 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_87397,RMVar_hsa_circ_104039,RMVar_hsa_circ_242681,RMVar_hsa_circ_27346,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_87043,RMVar_hsa_circ_122696,RMVar_hsa_circ_242695,RMVar_hsa_circ_242696,RMVar_hsa_circ_105107,RMVar_hsa_circ_242699,RMVar_hsa_circ_79528,RMVar_hsa_circ_242701,RMVar_hsa_circ_242702,RMVar_hsa_circ_298928 45001 RMVar_ID_45001 Human_SNP_ID_303388785 A-to-I Human chr6 + 158495273 158495273 158495273 CAGGGTTTCACCACATTGTCCATGCTGGTCTCAAACTCCTGAGCTCAAGCAATTTGCCCACCTCA CAGGGTTTCACCACATTGTCCATGCTGGTCTCCAACTCCTGAGCTCAAGCAATTTGCCCACCTCA A C TULP4 Ensembl:ENSG00000130338 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1554296896 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104039,RMVar_hsa_circ_27346,RMVar_hsa_circ_12683,RMVar_hsa_circ_94481,RMVar_hsa_circ_242693,RMVar_hsa_circ_242694,RMVar_hsa_circ_122696,RMVar_hsa_circ_242695,RMVar_hsa_circ_105107,RMVar_hsa_circ_242699,RMVar_hsa_circ_79528,RMVar_hsa_circ_102728,RMVar_hsa_circ_242701,RMVar_hsa_circ_307405,RMVar_hsa_circ_104031,RMVar_hsa_circ_242704,RMVar_hsa_circ_242705,RMVar_hsa_circ_242706 45002 RMVar_ID_45002 Human_SNP_ID_303409996 A-to-I Human chr6 + 158570601 158570601 158570601 GGGAAACAGGTCTGGAGTCAGTATACGTGCCCAAGATGCTGCAGCCCTGCCCTCTGCACCCACAC GGGAAACAGGTCTGGAGTCAGTATACGTGCCCGAGATGCTGCAGCCCTGCCCTCTGCACCCACAC A G TMEM181 Ensembl:ENSG00000146433 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1252871650 Functional Loss SNV dbSNP153 33..33 33 - - - 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,RMVar_hsa_circ_90381,RMVar_hsa_circ_242716 45003 RMVar_ID_45003 Human_SNP_ID_303410006 A-to-I Human chr6 + 158570645 158570645 158570645 CCCTGCCCTCTGCACCCACACTCTGCAGAGGTAGCTCTGAGACAGCGCTGCAGGCTCCAACCTAC CCCTGCCCTCTGCACCCACACTCTGCAGAGGTGGCTCTGAGACAGCGCTGCAGGCTCCAACCTAC A G TMEM181 Ensembl:ENSG00000146433 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1368569776 Functional Loss SNV dbSNP153 33..33 33 - - - 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,RMVar_hsa_circ_90381,RMVar_hsa_circ_242716 45004 RMVar_ID_45004 Human_SNP_ID_303410533 A-to-I Human chr6 + 158571745 158571745 158571745 ACTTTGCAGGGCTTGCCCAGAGGAGTTGGTGTAGGTTGGAGCCTGCAGCGCCGTCCCAGAGCAAC ACTTTGCAGGGCTTGCCCAGAGGAGTTGGTGTGGGTTGGAGCCTGCAGCGCCGTCCCAGAGCAAC A G TMEM181 Ensembl:ENSG00000146433 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1268843183 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26793364 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,RMVar_hsa_circ_90381,RMVar_hsa_circ_242716 45005 RMVar_ID_45005 Human_SNP_ID_303410545 A-to-I Human chr6 + 158571791 158571791 158571791 AGCGCCGTCCCAGAGCAACCTCTGTGCAGTGCAGGTGCAGAGGGCAGGGCTGCAGCATCTTGGGC AGCGCCGTCCCAGAGCAACCTCTGTGCAGTGCCGGTGCAGAGGGCAGGGCTGCAGCATCTTGGGC A C TMEM181 Ensembl:ENSG00000146433 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054626546 Functional Loss SNV dbSNP153 33..33 33 - - - 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,RMVar_hsa_circ_90381,RMVar_hsa_circ_242716 45006 RMVar_ID_45006 Human_SNP_ID_303410556 A-to-I Human chr6 + 158571826 158571826 158571826 TGCAGAGGGCAGGGCTGCAGCATCTTGGGCACATGCACTCTCTCCAGACCTCACTTTCCCCACCT TGCAGAGGGCAGGGCTGCAGCATCTTGGGCACGTGCACTCTCTCCAGACCTCACTTTCCCCACCT A G TMEM181 Ensembl:ENSG00000146433 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs531164202 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22728422 Human_miRNA_ID_2006678,Human_miRNA_ID_2792282 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,RMVar_hsa_circ_90381,RMVar_hsa_circ_242716 45007 RMVar_ID_45007 Human_SNP_ID_303445692 A-to-I Human chr6 + 158696385 158696384 158696386 CCACGCCTAATTTTTTTTTTTTTTTGTATTTTAGTAGAGATGGGGTTTCACTGTGTTGGCCAGTA CCACGCCTAATTTTTTTTTTTTTTTGTATTTT__TAGAGATGGGGTTTCACTGTGTTGGCCAGTA TAG T SYTL3 Ensembl:ENSG00000164674 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1380925191 Functional Loss DEL dbSNP153 33..34 33 - - - 45008 RMVar_ID_45008 Human_SNP_ID_303445693 A-to-I Human chr6 + 158696385 158696385 158696385 CCACGCCTAATTTTTTTTTTTTTTTGTATTTTAGTAGAGATGGGGTTTCACTGTGTTGGCCAGTA CCACGCCTAATTTTTTTTTTTTTTTGTATTTTTGTAGAGATGGGGTTTCACTGTGTTGGCCAGTA A T SYTL3 Ensembl:ENSG00000164674 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1414151681 Functional Loss SNV dbSNP153 33..33 33 - - - 45009 RMVar_ID_45009 Human_SNP_ID_303446549 A-to-I Human chr6 + 158699728 158699728 158699728 CCGGCACTTTGGGAGGCTGAGGTGGGAGGATCACTTGAGTTCAGGAGTTCGAGACCACCTTGGCC CCGGCACTTTGGGAGGCTGAGGTGGGAGGATCGCTTGAGTTCAGGAGTTCGAGACCACCTTGGCC A G SYTL3 Ensembl:ENSG00000164674 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1485383568 Functional Loss SNV dbSNP153 33..33 33 - - - 45010 RMVar_ID_45010 Human_SNP_ID_303469719 A-to-I Human chr6 - 158777674 158777674 158777674 TTGATGTGATCATAACGAAACCTGTATTGCTCATCAGTATTGAAGCTGTTGGTAGGCCATAGATT TTGATGTGATCATAACGAAACCTGTATTGCTCTTCAGTATTGAAGCTGTTGGTAGGCCATAGATT T A EZR Ensembl:ENSG00000092820 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs3127205 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_242772,RMVar_hsa_circ_86438,RMVar_hsa_circ_107253,RMVar_hsa_circ_125699,RMVar_hsa_circ_117290,RMVar_hsa_circ_91261,RMVar_hsa_circ_242776,RMVar_hsa_circ_83509,RMVar_hsa_circ_242774,RMVar_hsa_circ_242775,RMVar_hsa_circ_242773,RMVar_hsa_circ_124652,RMVar_hsa_circ_242771,RMVar_hsa_circ_295008,RMVar_hsa_circ_242783,RMVar_hsa_circ_364284,RMVar_hsa_circ_267771,RMVar_hsa_circ_323222,RMVar_hsa_circ_242785,RMVar_hsa_circ_242786 45011 RMVar_ID_45011 Human_SNP_ID_303469720 A-to-I Human chr6 - 158777674 158777674 158777674 TTGATGTGATCATAACGAAACCTGTATTGCTCATCAGTATTGAAGCTGTTGGTAGGCCATAGATT TTGATGTGATCATAACGAAACCTGTATTGCTCGTCAGTATTGAAGCTGTTGGTAGGCCATAGATT T C EZR Ensembl:ENSG00000092820 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs3127205 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_242772,RMVar_hsa_circ_86438,RMVar_hsa_circ_107253,RMVar_hsa_circ_125699,RMVar_hsa_circ_117290,RMVar_hsa_circ_91261,RMVar_hsa_circ_242776,RMVar_hsa_circ_83509,RMVar_hsa_circ_242774,RMVar_hsa_circ_242775,RMVar_hsa_circ_242773,RMVar_hsa_circ_124652,RMVar_hsa_circ_242771,RMVar_hsa_circ_295008,RMVar_hsa_circ_242783,RMVar_hsa_circ_364284,RMVar_hsa_circ_267771,RMVar_hsa_circ_323222,RMVar_hsa_circ_242785,RMVar_hsa_circ_242786 45012 RMVar_ID_45012 Human_SNP_ID_303469726 A-to-I Human chr6 - 158777698 158777696 158777699 GTCCACCCCACTGCCTTGATCTAGTTGATGTGATCATAACGAAACCTGTATTGCTCATCAGTATT GTCCACCCCACTGCCTTGATCTAGTTGATGT___CATAACGAAACCTGTATTGCTCATCAGTATT GATC G EZR Ensembl:ENSG00000092820 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1286745384 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_242772,RMVar_hsa_circ_86438,RMVar_hsa_circ_107253,RMVar_hsa_circ_125699,RMVar_hsa_circ_117290,RMVar_hsa_circ_91261,RMVar_hsa_circ_242776,RMVar_hsa_circ_83509,RMVar_hsa_circ_242774,RMVar_hsa_circ_242775,RMVar_hsa_circ_242773,RMVar_hsa_circ_124652,RMVar_hsa_circ_242771,RMVar_hsa_circ_295008,RMVar_hsa_circ_242783,RMVar_hsa_circ_364284,RMVar_hsa_circ_267771,RMVar_hsa_circ_323222,RMVar_hsa_circ_242785,RMVar_hsa_circ_242786 45013 RMVar_ID_45013 Human_SNP_ID_303469727 A-to-I Human chr6 - 158777698 158777698 158777698 GTCCACCCCACTGCCTTGATCTAGTTGATGTGATCATAACGAAACCTGTATTGCTCATCAGTATT GTCCACCCCACTGCCTTGATCTAGTTGATGTGGTCATAACGAAACCTGTATTGCTCATCAGTATT T C EZR Ensembl:ENSG00000092820 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs3102971 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5118,GWAS_ID_5119,GWAS_ID_5120 RMVar_hsa_circ_242772,RMVar_hsa_circ_86438,RMVar_hsa_circ_107253,RMVar_hsa_circ_125699,RMVar_hsa_circ_117290,RMVar_hsa_circ_91261,RMVar_hsa_circ_242776,RMVar_hsa_circ_83509,RMVar_hsa_circ_242774,RMVar_hsa_circ_242775,RMVar_hsa_circ_242773,RMVar_hsa_circ_124652,RMVar_hsa_circ_242771,RMVar_hsa_circ_295008,RMVar_hsa_circ_242783,RMVar_hsa_circ_364284,RMVar_hsa_circ_267771,RMVar_hsa_circ_323222,RMVar_hsa_circ_242785,RMVar_hsa_circ_242786 45014 RMVar_ID_45014 Human_SNP_ID_303507446 A-to-I Human chr6 - 158921844 158921844 158921844 AGAAAGTACTAGATGAATTCTCCAAGCAAGTCAACAGGATAGACTGGCCAGAAGGATCCCCTGCT AGAAAGTACTAGATGAATTCTCCAAGCAAGTCGACAGGATAGACTGGCCAGAAGGATCCCCTGCT T C AL627422.1 Ensembl:ENSG00000213076 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049509131 Functional Loss SNV dbSNP153 33..33 33 - - - 45015 RMVar_ID_45015 Human_SNP_ID_303519828 A-to-I Human chr6 - 158973480 158973480 158973480 TATGAAAGGGTGGGTAACTTGCAGAAGAAAGTATTTGGAGCCTATAATTCCATTAAAAGTTATAA TATGAAAGGGTGGGTAACTTGCAGAAGAAAGTGTTTGGAGCCTATAATTCCATTAAAAGTTATAA T C RSPH3 Ensembl:ENSG00000130363 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs566786837 Functional Loss SNV dbSNP153 33..33 33 - - - 45016 RMVar_ID_45016 Human_SNP_ID_303519834 A-to-I Human chr6 - 158973506 158973506 158973506 CAGTCTAGTGTTTCATTTTAAAAACATATGAAAGGGTGGGTAACTTGCAGAAGAAAGTATTTGGA CAGTCTAGTGTTTCATTTTAAAAACATATGAAGGGGTGGGTAACTTGCAGAAGAAAGTATTTGGA T C RSPH3 Ensembl:ENSG00000130363 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs557421417 Functional Loss SNV dbSNP153 33..33 33 - - - 45017 RMVar_ID_45017 Human_SNP_ID_303520027 A-to-I Human chr6 - 158974276 158974276 158974276 TGACCCTCAGTATGACTTTTAAAGGAATTATAAGCTCCAAATACTTTTTGGAGTATAAACAGTAC TGACCCTCAGTATGACTTTTAAAGGAATTATAGGCTCCAAATACTTTTTGGAGTATAAACAGTAC T C RSPH3 Ensembl:ENSG00000130363 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054759 Functional Loss SNV dbSNP153 33..33 33 - - - 45018 RMVar_ID_45018 Human_SNP_ID_303520028 A-to-I Human chr6 - 158974279 158974279 158974279 CTATGACCCTCAGTATGACTTTTAAAGGAATTATAAGCTCCAAATACTTTTTGGAGTATAAACAG CTATGACCCTCAGTATGACTTTTAAAGGAATTGTAAGCTCCAAATACTTTTTGGAGTATAAACAG T C RSPH3 Ensembl:ENSG00000130363 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054758 Functional Loss SNV dbSNP153 33..33 33 - - - 45019 RMVar_ID_45019 Human_SNP_ID_303520042 A-to-I Human chr6 - 158974321 158974321 158974321 TCATAACAGTTTGATGTGATATGCAAAATGCTACATCCCCAACTATGACCCTCAGTATGACTTTT TCATAACAGTTTGATGTGATATGCAAAATGCTGCATCCCCAACTATGACCCTCAGTATGACTTTT T C RSPH3 Ensembl:ENSG00000130363 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs768162242 Functional Loss SNV dbSNP153 33..33 33 - - - 45020 RMVar_ID_45020 Human_SNP_ID_303520052 A-to-I Human chr6 - 158974402 158974402 158974402 TTGCAAATGGTTTGGGAACATAAAACTCTTCCAGCATAGAAGAAAATGGGTACTATTAACATTCA TTGCAAATGGTTTGGGAACATAAAACTCTTCCGGCATAGAAGAAAATGGGTACTATTAACATTCA T C RSPH3 Ensembl:ENSG00000130363 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs983349828 Functional Loss SNV dbSNP153 33..33 33 - - - 45021 RMVar_ID_45021 Human_SNP_ID_303696690 A-to-I Human chr6 - 159669610 159669610 159669610 GTAGAGATGGGGTTATGCTATGTTGCCTGGCTAGTCTCAAACTCTGGGTCTCAAAGCAGTCCTCC GTAGAGATGGGGTTATGCTATGTTGCCTGGCTGGTCTCAAACTCTGGGTCTCAAAGCAGTCCTCC T C SOD2 Ensembl:ENSG00000112096 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1449889409 Functional Loss SNV dbSNP153 33..33 33 - - - 45022 RMVar_ID_45022 Human_SNP_ID_303696693 A-to-I Human chr6 - 159669623 159669623 159669623 AGAAAATTTTTTTGTAGAGATGGGGTTATGCTATGTTGCCTGGCTAGTCTCAAACTCTGGGTCTC AGAAAATTTTTTTGTAGAGATGGGGTTATGCTGTGTTGCCTGGCTAGTCTCAAACTCTGGGTCTC T C SOD2 Ensembl:ENSG00000112096 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs981305324 Functional Loss SNV dbSNP153 33..33 33 - - - 45023 RMVar_ID_45023 Human_SNP_ID_303699257 A-to-I Human chr6 - 159679899 159679899 159679899 TTTAGGGCTGGGCGGGGTGACTCACATCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGCAGA TTTAGGGCTGGGCGGGGTGACTCACATCTGTATTCCCAGCACTTTGGGAGGCCAAGGCAGGCAGA T A SOD2,SOD2:2 Ensembl:ENSG00000112096,Ensembl:ENSG00000285441 Protein coding,Protein coding 3'UTR,intron GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs1311942691 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_656382,Human_RBP_ID_7567425,Human_RBP_ID_8215815,Human_RBP_ID_26539663 Human_miRNA_ID_343419,Human_miRNA_ID_587228,Human_miRNA_ID_1360324,Human_miRNA_ID_1591139,Human_miRNA_ID_1695717 45024 RMVar_ID_45024 Human_SNP_ID_303699272 A-to-I Human chr6 - 159679938 159679938 159679938 GATTTTAGTCATCTGGTGGAAAAGGAGACTTTAAGATTGTTTAGGGCTGGGCGGGGTGACTCACA GATTTTAGTCATCTGGTGGAAAAGGAGACTTTGAGATTGTTTAGGGCTGGGCGGGGTGACTCACA T C SOD2,SOD2:2 Ensembl:ENSG00000112096,Ensembl:ENSG00000285441 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1312914047 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_656382,Human_RBP_ID_2987405,Human_RBP_ID_4871382,Human_RBP_ID_7567425,Human_RBP_ID_8635709,Human_RBP_ID_8898042,Human_RBP_ID_10268889,Human_RBP_ID_15714104,Human_RBP_ID_18085611,Human_RBP_ID_18367943,Human_RBP_ID_24144593,Human_RBP_ID_26539663 45025 RMVar_ID_45025 Human_SNP_ID_303699416 A-to-I Human chr6 - 159680692 159680692 159680692 ACCTCAAGTGATCCGTCTGGCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACTGCAC ACCTCAAGTGATCCGTCTGGCTCAGCCTCCCACAGTGCTGGGATTACAGGTGTGAGCCACTGCAC T G SOD2,SOD2:2 Ensembl:ENSG00000112096,Ensembl:ENSG00000285441 Protein coding,Protein coding 3'UTR,intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs980827212 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_656416,Human_RBP_ID_15714156 Human_miRNA_ID_973236 45026 RMVar_ID_45026 Human_SNP_ID_303699417 A-to-I Human chr6 - 159680693 159680693 159680693 GACCTCAAGTGATCCGTCTGGCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACTGCA GACCTCAAGTGATCCGTCTGGCTCAGCCTCCCGAAGTGCTGGGATTACAGGTGTGAGCCACTGCA T C SOD2,SOD2:2 Ensembl:ENSG00000112096,Ensembl:ENSG00000285441 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1475281261 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_656416,Human_RBP_ID_15714156 Human_miRNA_ID_973236 45027 RMVar_ID_45027 Human_SNP_ID_303699434 A-to-I Human chr6 - 159680756 159680756 159680756 ACTTTTTGTATTTTTAGCAGAGACAGGGTTTCACCATGTTGGCCAGGGTGGTCTCGAACTCCTGA ACTTTTTGTATTTTTAGCAGAGACAGGGTTTCTCCATGTTGGCCAGGGTGGTCTCGAACTCCTGA T A SOD2,SOD2:2 Ensembl:ENSG00000112096,Ensembl:ENSG00000285441 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1323326534 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15922477,Human_RBP_ID_26540347 45028 RMVar_ID_45028 Human_SNP_ID_303709721 A-to-I Human chr6 - 159715608 159715608 159715608 GGCGTGAGCCACCATGCCTGGCCTATATTCAGAACTTTTCAAAATACTATTCTGTTTGCCTCTGT GGCGTGAGCCACCATGCCTGGCCTATATTCAGGACTTTTCAAAATACTATTCTGTTTGCCTCTGT T C SOD2,SOD2:2 Ensembl:ENSG00000112096,Ensembl:ENSG00000285441 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs73599364 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15714646 45029 RMVar_ID_45029 Human_SNP_ID_303711500 A-to-I Human chr6 - 159722327 159722327 159722327 CAGGCTGGAGTGCAGTGGCACAAACATGGCTCACTGCAGTCTTGACCTCCTGGGCTCAAGTGATC CAGGCTGGAGTGCAGTGGCACAAACATGGCTCGCTGCAGTCTTGACCTCCTGGGCTCAAGTGATC T C SOD2,SOD2:2 Ensembl:ENSG00000112096,Ensembl:ENSG00000285441 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1273769139 Functional Loss SNV dbSNP153 33..33 33 - - - 45030 RMVar_ID_45030 Human_SNP_ID_303715253 A-to-I Human chr6 + 159734242 159734242 159734242 TACCACATTGCCCGGGCTCGGTTCAAACTCCTAGGCTCAAGCAGCTCTCCTGCCTCAGCCTCCCA TACCACATTGCCCGGGCTCGGTTCAAACTCCTGGGCTCAAGCAGCTCTCCTGCCTCAGCCTCCCA A G WTAP Ensembl:ENSG00000146457 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1349234246 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24144739 RMVar_hsa_circ_113323,RMVar_hsa_circ_78999,RMVar_hsa_circ_242804,RMVar_hsa_circ_95697,RMVar_hsa_circ_242805,RMVar_hsa_circ_242806 45031 RMVar_ID_45031 Human_SNP_ID_303715546 A-to-I Human chr6 + 159735240 159735240 159735240 TCGGCTCACTGCAACCTCCGCCTCCCAGGTTCAGGCGATTCCTGCCTCAGTCTCCCTAGTAGCTG TCGGCTCACTGCAACCTCCGCCTCCCAGGTTCGGGCGATTCCTGCCTCAGTCTCCCTAGTAGCTG A G WTAP Ensembl:ENSG00000146457 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1042707032 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113323,RMVar_hsa_circ_78999,RMVar_hsa_circ_242804,RMVar_hsa_circ_95697,RMVar_hsa_circ_242805,RMVar_hsa_circ_242806 45032 RMVar_ID_45032 Human_SNP_ID_303715573 A-to-I Human chr6 + 159735324 159735324 159735324 CTACGCCGGGCTAATTTTTTTAATTTTTTGGTAGAGACCGAGTTTCACCATGTTGGCCAGACTTG CTACGCCGGGCTAATTTTTTTAATTTTTTGGTGGAGACCGAGTTTCACCATGTTGGCCAGACTTG A G WTAP Ensembl:ENSG00000146457 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs928235384 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113323,RMVar_hsa_circ_78999,RMVar_hsa_circ_242804,RMVar_hsa_circ_95697,RMVar_hsa_circ_242805,RMVar_hsa_circ_242806 45033 RMVar_ID_45033 Human_SNP_ID_303715615 A-to-I Human chr6 + 159735495 159735495 159735495 GTAATAGGATGGGCGTGGTGGTTCATTCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGACGG GTAATAGGATGGGCGTGGTGGTTCATTCCTGTGATCCCAGCACTTTGGGAGGCCAAGGCGGACGG A G WTAP Ensembl:ENSG00000146457 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1490289884 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113323,RMVar_hsa_circ_78999,RMVar_hsa_circ_242804,RMVar_hsa_circ_95697,RMVar_hsa_circ_242805,RMVar_hsa_circ_242806 45034 RMVar_ID_45034 Human_SNP_ID_303725271 A-to-I Human chr6 + 159770801 159770796 159770802 AGAATAAATGAACAGGCCAGGCACGGTAGCTCACGCTTGTAATCCCAGCACTTTGGGAGGCCAAG AGAATAAATGAACAGGCCAGGCACGGTA______GCTTGTAATCCCAGCACTTTGGGAGGCCAAG AGCTCAC A ACAT2 Ensembl:ENSG00000120437 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1283702826 Functional Loss DEL dbSNP153 29..34 33 - - - Human_RBP_ID_17663500 RMVar_hsa_circ_15253,RMVar_hsa_circ_322230,RMVar_hsa_circ_75802,RMVar_hsa_circ_242813,RMVar_hsa_circ_242814 45035 RMVar_ID_45035 Human_SNP_ID_303727491 A-to-I Human chr6 + 159778829 159778829 159778829 ATGGGAATAGCAATGTGTGTTCAGAGAGAATGAATTGCTTAAACTTTGAACAACCTCAATTTCTT ATGGGAATAGCAATGTGTGTTCAGAGAGAATGGATTGCTTAAACTTTGAACAACCTCAATTTCTT A G ACAT2 Ensembl:ENSG00000120437 Protein coding stop codon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031275056 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2013232,Human_RBP_ID_5152255,Human_RBP_ID_9309449,Human_RBP_ID_17663842,Human_RBP_ID_18068801,Human_RBP_ID_24144848 45036 RMVar_ID_45036 Human_SNP_ID_303733553 A-to-I Human chr6 + 159797434 159797434 159797434 ACCAGAAATGTGGTGGCTTGTGAGAGTATAGGACGAGTGCTGGCACAGAGATGCTTAGAGGCGGG ACCAGAAATGTGGTGGCTTGTGAGAGTATAGGGCGAGTGCTGGCACAGAGATGCTTAGAGGCGGG A G MRPL18 Ensembl:ENSG00000112110 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1266516236 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_656628,Human_RBP_ID_1325671,Human_RBP_ID_2013301,Human_RBP_ID_4871851,Human_RBP_ID_7568229,Human_RBP_ID_15716231,Human_RBP_ID_17663844,Human_RBP_ID_24144911,Human_RBP_ID_26533548,Human_RBP_ID_27342588 Human_Splice_Rec_829571,Human_Splice_Rec_829583,Human_Splice_Rec_829589 Human_miRNA_ID_2439546 RMVar_hsa_circ_242830,RMVar_hsa_circ_76188,RMVar_hsa_circ_118656,RMVar_hsa_circ_242831 45037 RMVar_ID_45037 Human_SNP_ID_303800047 A-to-I Human chr6 + 160053811 160053811 160053811 CTGAATCACTGCAGCCTCGACTTCCTGGGCTCAAGTGACCCTGTCACCTCAGCCTCCTGAGTAGC CTGAATCACTGCAGCCTCGACTTCCTGGGCTCGAGTGACCCTGTCACCTCAGCCTCCTGAGTAGC A G IGF2R Ensembl:ENSG00000197081 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1161544551 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121692,RMVar_hsa_circ_242836,RMVar_hsa_circ_119716,RMVar_hsa_circ_242837,RMVar_hsa_circ_94363,RMVar_hsa_circ_111491,RMVar_hsa_circ_242839,RMVar_hsa_circ_242840,RMVar_hsa_circ_75765,RMVar_hsa_circ_92773,RMVar_hsa_circ_242842,RMVar_hsa_circ_242843,RMVar_hsa_circ_111896,RMVar_hsa_circ_11274,RMVar_hsa_circ_242845,RMVar_hsa_circ_112156,RMVar_hsa_circ_242848,RMVar_hsa_circ_110511,RMVar_hsa_circ_86895,RMVar_hsa_circ_77685,RMVar_hsa_circ_107801,RMVar_hsa_circ_110393,RMVar_hsa_circ_242849,RMVar_hsa_circ_242850,RMVar_hsa_circ_100975,RMVar_hsa_circ_242852,RMVar_hsa_circ_242853,RMVar_hsa_circ_242854,RMVar_hsa_circ_80830,RMVar_hsa_circ_107945,RMVar_hsa_circ_112124,RMVar_hsa_circ_242856,RMVar_hsa_circ_242857,RMVar_hsa_circ_242855,RMVar_hsa_circ_9432,RMVar_hsa_circ_242858 45038 RMVar_ID_45038 Human_SNP_ID_303882870 A-to-I Human chr6 + 160376080 160376079 160376081 TGTGAAGTCTCAAAAAAAGTGAATTTTACAATAGCAAAGACATGGAACCAACCCAAATGCCCATC TGTGAAGTCTCAAAAAAAGTGAATTTTACAAT__CAAAGACATGGAACCAACCCAAATGCCCATC TAG T SLC22A3 Ensembl:ENSG00000146477 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1190849866 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_242871,RMVar_hsa_circ_102909 45039 RMVar_ID_45039 Human_SNP_ID_304477011 A-to-I Human chr6 - 162694203 162694203 162694203 TCTCACTGTTGCCCAGGCTGGAGTGCAGTGGCACGATCTCGGCTCACTGCAAGCTCCGCCTCCCA TCTCACTGTTGCCCAGGCTGGAGTGCAGTGGCGCGATCTCGGCTCACTGCAAGCTCCGCCTCCCA T C PRKN Ensembl:ENSG00000185345 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984857136 Functional Loss SNV dbSNP153 33..33 33 - - - 45040 RMVar_ID_45040 Human_SNP_ID_304657908 A-to-I Human chr6 + 163424811 163424811 163424811 GCACCTCCACACCCGGCTAATTGCTGTATTTTAGTAGAGACAGGGTTTCACCATGTTAGCCAGGC GCACCTCCACACCCGGCTAATTGCTGTATTTTGGTAGAGACAGGGTTTCACCATGTTAGCCAGGC A G QKI Ensembl:ENSG00000112531 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1340266364 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90197,RMVar_hsa_circ_242916 45041 RMVar_ID_45041 Human_SNP_ID_304657909 A-to-I Human chr6 + 163424811 163424811 163424811 GCACCTCCACACCCGGCTAATTGCTGTATTTTAGTAGAGACAGGGTTTCACCATGTTAGCCAGGC GCACCTCCACACCCGGCTAATTGCTGTATTTTTGTAGAGACAGGGTTTCACCATGTTAGCCAGGC A T QKI Ensembl:ENSG00000112531 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1340266364 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90197,RMVar_hsa_circ_242916 45042 RMVar_ID_45042 Human_SNP_ID_304659967 A-to-I Human chr6 + 163432603 163432603 163432603 TTTTTTTTTGGTAAGAGACAGGGTCTCACGATATTGCCCAGCCTGGTCTTAAACTTAAGGCCTCA TTTTTTTTTGGTAAGAGACAGGGTCTCACGATGTTGCCCAGCCTGGTCTTAAACTTAAGGCCTCA A G QKI Ensembl:ENSG00000112531 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs955475892 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_842003 RMVar_hsa_circ_90197,RMVar_hsa_circ_242916 45043 RMVar_ID_45043 Human_SNP_ID_304662785 A-to-I Human chr6 + 163443382 163443382 163443382 TACGAGGTCAGGAGTTCAAAACCAGCCTGGCCAAGATGGTGAAATGCTGTCTCTGCTAAAAATAC TACGAGGTCAGGAGTTCAAAACCAGCCTGGCCGAGATGGTGAAATGCTGTCTCTGCTAAAAATAC A G QKI Ensembl:ENSG00000112531 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs916187920 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90197,RMVar_hsa_circ_242916 45044 RMVar_ID_45044 Human_SNP_ID_304715752 A-to-I Human chr6 + 163643211 163643208 163643211 AGGTTCACGCCATTCTCCTGCCTCAGCCTCCCAAGCAGCCGGGACCATAGGCGCCCGCCACCACG AGGTTCACGCCATTCTCCTGCCTCAGCCTC___AGCAGCCGGGACCATAGGCGCCCGCCACCACG CCCA C lnc-QKI-7,lnc-QKI-7:2 RNACentral:URS00008B64F8,RNACentral:URS00008B8DB0 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1310474751 Functional Loss DEL dbSNP153 31..33 33 - - - 45045 RMVar_ID_45045 Human_SNP_ID_304715754 A-to-I Human chr6 + 163643211 163643211 163643211 AGGTTCACGCCATTCTCCTGCCTCAGCCTCCCAAGCAGCCGGGACCATAGGCGCCCGCCACCACG AGGTTCACGCCATTCTCCTGCCTCAGCCTCCCGAGCAGCCGGGACCATAGGCGCCCGCCACCACG A G lnc-QKI-7,lnc-QKI-7:2 RNACentral:URS00008B64F8,RNACentral:URS00008B8DB0 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1194828994 Functional Loss SNV dbSNP153 33..33 33 - - - 45046 RMVar_ID_45046 Human_SNP_ID_438100507 A-to-I Human chr10 + 75116909 75116909 75116909 TCAGTTCATAGCAACCTTCGCCTCCCGGGTTCAAGCAATTCTCCCACCTCAGCCTCCCCAGTAGC TCAGTTCATAGCAACCTTCGCCTCCCGGGTTCGAGCAATTCTCCCACCTCAGCCTCCCCAGTAGC A G SAMD8 Ensembl:ENSG00000156671 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs923331085 Functional Loss SNV dbSNP153 33..33 33 - - - 45047 RMVar_ID_45047 Human_SNP_ID_438100508 A-to-I Human chr10 + 75116913 75116913 75116913 TTCATAGCAACCTTCGCCTCCCGGGTTCAAGCAATTCTCCCACCTCAGCCTCCCCAGTAGCTGGG TTCATAGCAACCTTCGCCTCCCGGGTTCAAGCTATTCTCCCACCTCAGCCTCCCCAGTAGCTGGG A T SAMD8 Ensembl:ENSG00000156671 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1396344081 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24836387 45048 RMVar_ID_45048 Human_SNP_ID_438100517 A-to-I Human chr10 + 75116949 75116949 75116949 CTCCCACCTCAGCCTCCCCAGTAGCTGGGATTACAGGCGCGTGCCACCATGCTCGGCTAATTTTT CTCCCACCTCAGCCTCCCCAGTAGCTGGGATTCCAGGCGCGTGCCACCATGCTCGGCTAATTTTT A C SAMD8 Ensembl:ENSG00000156671 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1204640277 Functional Loss SNV dbSNP153 33..33 33 - - - 45049 RMVar_ID_45049 Human_SNP_ID_438100526 A-to-I Human chr10 + 75116975 75116975 75116975 GGGATTACAGGCGCGTGCCACCATGCTCGGCTAATTTTTTGTGTTTTTAGTAGAGACGAGGTCTC GGGATTACAGGCGCGTGCCACCATGCTCGGCTGATTTTTTGTGTTTTTAGTAGAGACGAGGTCTC A G SAMD8 Ensembl:ENSG00000156671 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7908748 Functional Loss SNV dbSNP153 33..33 33 - - - 45050 RMVar_ID_45050 Human_SNP_ID_438100609 A-to-I Human chr10 + 75117366 75117366 75117366 ATCACCTGAGCCCAGGAGGTCAAAGCTGCAGTAAGCTGTGATTGCGCCACTGCACTCCAGCCTGG ATCACCTGAGCCCAGGAGGTCAAAGCTGCAGTGAGCTGTGATTGCGCCACTGCACTCCAGCCTGG A G SAMD8 Ensembl:ENSG00000156671 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1342359598 Functional Loss SNV dbSNP153 33..33 33 - - - 45051 RMVar_ID_45051 Human_SNP_ID_438101857 A-to-I Human chr10 + 75122458 75122458 75122458 ACATGGCAAAACCCTGTCTCCAGAAAAAAAATAGAAAAATTAGCTGAGCGTGGTGGGGGCACCAG ACATGGCAAAACCCTGTCTCCAGAAAAAAAATGGAAAAATTAGCTGAGCGTGGTGGGGGCACCAG A G SAMD8 Ensembl:ENSG00000156671 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs148456747 Functional Loss SNV dbSNP153 33..33 33 - - - 45052 RMVar_ID_45052 Human_SNP_ID_438109390 A-to-I Human chr10 + 75153507 75153507 75153507 GTGGCGGACACCTGTAATTATCTCAGCTACTCAGGAGACTGAGGCAGGAGAATTGCTTGAACCTG GTGGCGGACACCTGTAATTATCTCAGCTACTCTGGAGACTGAGGCAGGAGAATTGCTTGAACCTG A T SAMD8 Ensembl:ENSG00000156671 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027493200 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_144462,RMVar_hsa_circ_277154,RMVar_hsa_circ_296678,RMVar_hsa_circ_270065,RMVar_hsa_circ_144460,RMVar_hsa_circ_144461 45053 RMVar_ID_45053 Human_SNP_ID_438112903 A-to-I Human chr10 + 75167827 75167827 75167827 GTTGCCCAAGCTGTTGTCAAACTTTTGGACTCAAGCAATCCTCCCACCTTGGCCTCCCAAAGGGC GTTGCCCAAGCTGTTGTCAAACTTTTGGACTCTAGCAATCCTCCCACCTTGGCCTCCCAAAGGGC A T SAMD8 Ensembl:ENSG00000156671 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917318924 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_144463,RMVar_hsa_circ_144462,RMVar_hsa_circ_277154,RMVar_hsa_circ_296678,RMVar_hsa_circ_144461,RMVar_hsa_circ_284269 45054 RMVar_ID_45054 Human_SNP_ID_438116116 A-to-I Human chr10 + 75181640 75181640 75181640 GCATAAGGAAAGTTTGTGCCTGATATGGCAGGAGAAAGAACACTATGGTAATTTCATTGTTACTT GCATAAGGAAAGTTTGTGCCTGATATGGCAGGGGAAAGAACACTATGGTAATTTCATTGTTACTT A G SAMD8 Ensembl:ENSG00000156671 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs201863816 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_382932,Human_RBP_ID_6003050,Human_RBP_ID_11433439,Human_RBP_ID_18244198,Human_RBP_ID_27611110 RMVar_hsa_circ_144468,RMVar_hsa_circ_144464 45055 RMVar_ID_45055 Human_SNP_ID_438124873 A-to-I Human chr10 + 75215534 75215534 75215534 CCACCACGCCCAGCTAATTTTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTAGCCAGGA CCACCACGCCCAGCTAATTTTTTTGTATTTTTGGTAGAGATGGGGTTTCACCATGTTAGCCAGGA A G VDAC2 Ensembl:ENSG00000165637 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1034053586 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83688,RMVar_hsa_circ_144471,RMVar_hsa_circ_144470,RMVar_hsa_circ_373376,RMVar_hsa_circ_37063,RMVar_hsa_circ_375079,RMVar_hsa_circ_144472 45056 RMVar_ID_45056 Human_SNP_ID_438125001 A-to-I Human chr10 + 75215887 75215887 75215887 GGGATTACAGGTGCTTGCCACCATGCCCCGCTAATTTTTGTATTTTTAGTAGAAACAGGGTTTTG GGGATTACAGGTGCTTGCCACCATGCCCCGCTTATTTTTGTATTTTTAGTAGAAACAGGGTTTTG A T VDAC2 Ensembl:ENSG00000165637 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1333031736 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83688,RMVar_hsa_circ_144471,RMVar_hsa_circ_144470,RMVar_hsa_circ_373376,RMVar_hsa_circ_37063,RMVar_hsa_circ_375079,RMVar_hsa_circ_144472 45057 RMVar_ID_45057 Human_SNP_ID_438264506 A-to-I Human chr10 + 75808579 75808579 75808579 GTTGCCAGGCTGGAGTGCAGTGGCGTGATCTCAGTTCACTGTAACTTCCGACTCCTTGGTTCAAG GTTGCCAGGCTGGAGTGCAGTGGCGTGATCTCTGTTCACTGTAACTTCCGACTCCTTGGTTCAAG A T LRMDA Ensembl:ENSG00000148655 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1402136729 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_144480 45058 RMVar_ID_45058 Human_SNP_ID_438264717 A-to-I Human chr10 + 75809482 75809482 75809482 CTGATCAACATAGTGAAACCCTGTCTCTACTAAAAGTACAAAAATTAGCCAGGCGTGGTGGTGTG CTGATCAACATAGTGAAACCCTGTCTCTACTACAAGTACAAAAATTAGCCAGGCGTGGTGGTGTG A C LRMDA Ensembl:ENSG00000148655 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1180778649 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_144480 45059 RMVar_ID_45059 Human_SNP_ID_438732954 A-to-I Human chr10 - 77786721 77786721 77786721 TTCTTTTCTTTTTTTTTTTTTTTTGAGACAGAATCTTATTCTGTCACCCAGGCTGGAGTGCAGAG TTCTTTTCTTTTTTTTTTTTTTTTGAGACAGAGTCTTATTCTGTCACCCAGGCTGGAGTGCAGAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1433505588 Functional Loss SNV dbSNP153 33..33 33 - - - 45060 RMVar_ID_45060 Human_SNP_ID_438735993 A-to-I Human chr10 - 77798189 77798189 77798189 TAATGATCAGTTTTATTATTTTATTTATTTTTATTGAGATCTAGTCTTGCTCTGTTGCCCAGGCT TAATGATCAGTTTTATTATTTTATTTATTTTTGTTGAGATCTAGTCTTGCTCTGTTGCCCAGGCT T C DLG5 Ensembl:ENSG00000151208 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs951125290 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11437736 RMVar_hsa_circ_37984,RMVar_hsa_circ_1280,RMVar_hsa_circ_96205,RMVar_hsa_circ_144521 45061 RMVar_ID_45061 Human_SNP_ID_438738465 A-to-I Human chr10 - 77808352 77808352 77808352 TGAGGTGGGAGGATCACTTGAGCCTAAGAGGTATAGGCTACTGTGAGCTGTGATTGCACCACTGC TGAGGTGGGAGGATCACTTGAGCCTAAGAGGTTTAGGCTACTGTGAGCTGTGATTGCACCACTGC T A DLG5 Ensembl:ENSG00000151208 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs890483177 Functional Loss SNV dbSNP153 33..33 33 - - - 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_144522,RMVar_hsa_circ_144523 45062 RMVar_ID_45062 Human_SNP_ID_438738466 A-to-I Human chr10 - 77808352 77808352 77808352 TGAGGTGGGAGGATCACTTGAGCCTAAGAGGTATAGGCTACTGTGAGCTGTGATTGCACCACTGC TGAGGTGGGAGGATCACTTGAGCCTAAGAGGTGTAGGCTACTGTGAGCTGTGATTGCACCACTGC T C DLG5 Ensembl:ENSG00000151208 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs890483177 Functional Loss SNV dbSNP153 33..33 33 - - - 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_144522,RMVar_hsa_circ_144523 45063 RMVar_ID_45063 Human_SNP_ID_438740526 A-to-I Human chr10 - 77815614 77815614 77815614 TCTTTTCGCCCAGGCTGGAGTACAGTGGTGCAATCTTGGCTCACTGCAATCTCTGCCTCCCAAGT TCTTTTCGCCCAGGCTGGAGTACAGTGGTGCAGTCTTGGCTCACTGCAATCTCTGCCTCCCAAGT T C DLG5 Ensembl:ENSG00000151208 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559406510 Functional Loss SNV dbSNP153 33..33 33 - - - 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 45064 RMVar_ID_45064 Human_SNP_ID_438749137 A-to-I Human chr10 - 77847879 77847879 77847879 AACATAGTGAGACCCCCATCTCTACAAAAAATAAAAAATCAGCCAGGTGTGGTGGGGCGTGTCTG AACATAGTGAGACCCCCATCTCTACAAAAAATGAAAAATCAGCCAGGTGTGGTGGGGCGTGTCTG T C DLG5 Ensembl:ENSG00000151208 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1359242329 Functional Loss SNV dbSNP153 33..33 33 - - - 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_144531 45065 RMVar_ID_45065 Human_SNP_ID_438767510 A-to-I Human chr10 - 77923630 77923630 77923630 CCTCAGCCCCGCAAGTAGCTGGGACCACAGGCACATGCCACCACACCAGCTAATTTTTGTATATT CCTCAGCCCCGCAAGTAGCTGGGACCACAGGCGCATGCCACCACACCAGCTAATTTTTGTATATT T C DLG5 Ensembl:ENSG00000151208 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1276182434 Functional Loss SNV dbSNP153 33..33 33 - - - 45066 RMVar_ID_45066 Human_SNP_ID_438768995 A-to-I Human chr10 + 77929244 77929244 77929244 TTAAATATTTTGTAGACACAGGGTCTTGCCACATTGCCCAGGCTGGTCTTGAACTCCTGGGCTCA TTAAATATTTTGTAGACACAGGGTCTTGCCACGTTGCCCAGGCTGGTCTTGAACTCCTGGGCTCA A G DLG5-AS1 Ensembl:ENSG00000233871 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232743547 Functional Loss SNV dbSNP153 33..33 33 - - - 45067 RMVar_ID_45067 Human_SNP_ID_438778539 A-to-I Human chr10 - 77970552 77970552 77970552 TAATTTTAAATCTAGTATTGGCCAGGTATGGTAGCTCACGTCTGTAATCCCAGCACTTTGGGAGG TAATTTTAAATCTAGTATTGGCCAGGTATGGTGGCTCACGTCTGTAATCCCAGCACTTTGGGAGG T C POLR3A Ensembl:ENSG00000148606 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1323878201 Functional Loss SNV dbSNP153 33..33 33 - - - 45068 RMVar_ID_45068 Human_SNP_ID_438791706 A-to-I Human chr10 - 78021227 78021227 78021227 CATGGTGGCTAATGCCTGTAATCCCAATACTTAGGGAGGCCAAGGCAGGTGGATCATCCGAGCCC CATGGTGGCTAATGCCTGTAATCCCAATACTTGGGGAGGCCAAGGCAGGTGGATCATCCGAGCCC T C POLR3A Ensembl:ENSG00000148606 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1321034913 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11439292 RMVar_hsa_circ_127006,RMVar_hsa_circ_91692,RMVar_hsa_circ_78814,RMVar_hsa_circ_144547,RMVar_hsa_circ_144548,RMVar_hsa_circ_144546,RMVar_hsa_circ_196,RMVar_hsa_circ_9230,RMVar_hsa_circ_63641,RMVar_hsa_circ_92875,RMVar_hsa_circ_144554,RMVar_hsa_circ_366900,RMVar_hsa_circ_103563,RMVar_hsa_circ_5973,RMVar_hsa_circ_144564,RMVar_hsa_circ_268858,RMVar_hsa_circ_100799,RMVar_hsa_circ_38369,RMVar_hsa_circ_144566 45069 RMVar_ID_45069 Human_SNP_ID_438791709 A-to-I Human chr10 - 78021239 78021239 78021239 ATCTTGACCGAGCATGGTGGCTAATGCCTGTAATCCCAATACTTAGGGAGGCCAAGGCAGGTGGA ATCTTGACCGAGCATGGTGGCTAATGCCTGTAGTCCCAATACTTAGGGAGGCCAAGGCAGGTGGA T C POLR3A Ensembl:ENSG00000148606 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1220087293 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11439292 RMVar_hsa_circ_127006,RMVar_hsa_circ_91692,RMVar_hsa_circ_78814,RMVar_hsa_circ_144547,RMVar_hsa_circ_144548,RMVar_hsa_circ_144546,RMVar_hsa_circ_196,RMVar_hsa_circ_9230,RMVar_hsa_circ_63641,RMVar_hsa_circ_92875,RMVar_hsa_circ_144554,RMVar_hsa_circ_366900,RMVar_hsa_circ_103563,RMVar_hsa_circ_5973,RMVar_hsa_circ_144564,RMVar_hsa_circ_268858,RMVar_hsa_circ_100799,RMVar_hsa_circ_38369,RMVar_hsa_circ_144566 45070 RMVar_ID_45070 Human_SNP_ID_438797524 A-to-I Human chr10 - 78040200 78040200 78040200 ATTATACCTGTGATCCAATCTCCAGCTCACTGAATCAGTGGCGGGGAAGGGAAAAAGAGAAAGGA ATTATACCTGTGATCCAATCTCCAGCTCACTGCATCAGTGGCGGGGAAGGGAAAAAGAGAAAGGA T G - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs747183790 Functional Loss SNV dbSNP153 33..33 33 - - - 45071 RMVar_ID_45071 Human_SNP_ID_439110364 A-to-I Human chr10 + 79280172 79280172 79280172 ACCACCCATGGCTAATTTTTTGTATTTTTAGTAGAGATGGCATTGCCCAGGCTGGTCTCGAACTC ACCACCCATGGCTAATTTTTTGTATTTTTAGTGGAGATGGCATTGCCCAGGCTGGTCTCGAACTC A G ZMIZ1 Ensembl:ENSG00000108175 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1009279756 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_144582 45072 RMVar_ID_45072 Human_SNP_ID_439116827 A-to-I Human chr10 + 79303003 79303003 79303003 CCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCCACCACCGCACCTGGCTAATTTTTTG CCTGCCTCAGCCTCCCGAGTAGCTGGGACTACGGGCGCCCACCACCGCACCTGGCTAATTTTTTG A G ZMIZ1 Ensembl:ENSG00000108175 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1474829285 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_53288,RMVar_hsa_circ_19866 45073 RMVar_ID_45073 Human_SNP_ID_439116843 A-to-I Human chr10 + 79303045 79303045 79303045 CACCGCACCTGGCTAATTTTTTGTGTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGG CACCGCACCTGGCTAATTTTTTGTGTTTTAGTGGAGACGGGGTTTCACCGTGTTAGCCAGGATGG A G ZMIZ1 Ensembl:ENSG00000108175 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1450231497 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_53288,RMVar_hsa_circ_19866 45074 RMVar_ID_45074 Human_SNP_ID_439116914 A-to-I Human chr10 + 79303289 79303289 79303289 CTAGCCTGGCCGCATAGTGAGAGCCTGTCTCTACAGAAAAATAAAAAATTAGCCAGGTGTGGTGG CTAGCCTGGCCGCATAGTGAGAGCCTGTCTCTGCAGAAAAATAAAAAATTAGCCAGGTGTGGTGG A G ZMIZ1 Ensembl:ENSG00000108175 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1216350595 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17559089 RMVar_hsa_circ_53288,RMVar_hsa_circ_19866 45075 RMVar_ID_45075 Human_SNP_ID_439225724 A-to-I Human chr10 - 79732963 79732963 79732963 AAATGGCTGGGCTTACTTTGGGAGGCCGAGGCAGGTGGATCACTTGAGCCCAGGAGTTCAAGATC AAATGGCTGGGCTTACTTTGGGAGGCCGAGGCTGGTGGATCACTTGAGCCCAGGAGTTCAAGATC T A NUTM2B-AS1 Ensembl:ENSG00000225484 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1004525394 Functional Loss SNV dbSNP153 33..33 33 - - - 45076 RMVar_ID_45076 Human_SNP_ID_439231121 A-to-I Human chr10 - 79761195 79761195 79761195 TGGAGTGCAGTGATATGATCATAGCTCACTGCAGCCTTGAACTCCTGGGCTCCAGCAATCCTCCC TGGAGTGCAGTGATATGATCATAGCTCACTGCGGCCTTGAACTCCTGGGCTCCAGCAATCCTCCC T C NUTM2B-AS1 Ensembl:ENSG00000225484 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs919072452 Functional Loss SNV dbSNP153 33..33 33 - - - 45077 RMVar_ID_45077 Human_SNP_ID_439236437 A-to-I Human chr10 - 79785883 79785883 79785883 TCTCCCTGTCACCCAGACTGGAATGCAGTGGCATGATCTTGGTTCACTGAAACCTCTGCCTTTCT TCTCCCTGTCACCCAGACTGGAATGCAGTGGCGTGATCTTGGTTCACTGAAACCTCTGCCTTTCT T C NUTM2B-AS1 Ensembl:ENSG00000225484 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1235480662 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1155243 RMVar_hsa_circ_290828,RMVar_hsa_circ_297825,RMVar_hsa_circ_319060 45078 RMVar_ID_45078 Human_SNP_ID_439241640 A-to-I Human chr10 - 79804529 79804529 79804529 TCCTTTGTAATATAGTCCCTTTCTTCCCTTACAGGCTCATATGACATTAACAGACAAGACACTTT TCCTTTGTAATATAGTCCCTTTCTTCCCTTACGGGCTCATATGACATTAACAGACAAGACACTTT T C NUTM2B-AS1 Ensembl:ENSG00000225484 lincRNA intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1348502324 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1155157,Human_Splice_Rec_1155177,Human_Splice_Rec_1155189,Human_Splice_Rec_1155201,Human_Splice_Rec_1155209,Human_Splice_Rec_1155225,Human_Splice_Rec_1155239,Human_Splice_Rec_1155253,Human_Splice_Rec_1155261,Human_Splice_Rec_1155271,Human_Splice_Rec_1155279,Human_Splice_Rec_1155287,Human_Splice_Rec_1155297,Human_Splice_Rec_1155309,Human_Splice_Rec_1155319 RMVar_hsa_circ_46479,RMVar_hsa_circ_290828,RMVar_hsa_circ_297825,RMVar_hsa_circ_319060,RMVar_hsa_circ_313380,RMVar_hsa_circ_335238 45079 RMVar_ID_45079 Human_SNP_ID_439309692 A-to-I Human chr10 + 80079862 80079862 80079862 TACCTGTAGCTGGGATTACACTATGCCCAGCTATTTTTTTGTGTTTTTAGTAGACATGGGTATTG TACCTGTAGCTGGGATTACACTATGCCCAGCTTTTTTTTTGTGTTTTTAGTAGACATGGGTATTG A T TMEM254 Ensembl:ENSG00000133678 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1363437487 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17783605 RMVar_hsa_circ_144597,RMVar_hsa_circ_108528 45080 RMVar_ID_45080 Human_SNP_ID_439309699 A-to-I Human chr10 + 80079878 80079878 80079878 TACACTATGCCCAGCTATTTTTTTGTGTTTTTAGTAGACATGGGTATTGGTGAGGCTGGCCTCGA TACACTATGCCCAGCTATTTTTTTGTGTTTTTGGTAGACATGGGTATTGGTGAGGCTGGCCTCGA A G TMEM254 Ensembl:ENSG00000133678 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1440304120 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_144597,RMVar_hsa_circ_108528 45081 RMVar_ID_45081 Human_SNP_ID_439309700 A-to-I Human chr10 + 80079878 80079878 80079878 TACACTATGCCCAGCTATTTTTTTGTGTTTTTAGTAGACATGGGTATTGGTGAGGCTGGCCTCGA TACACTATGCCCAGCTATTTTTTTGTGTTTTTTGTAGACATGGGTATTGGTGAGGCTGGCCTCGA A T TMEM254 Ensembl:ENSG00000133678 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1440304120 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_144597,RMVar_hsa_circ_108528 45082 RMVar_ID_45082 Human_SNP_ID_439396617 A-to-I Human chr10 + 80430997 80430997 80430997 CTGCAACCTCCGCCTCCCAGCCTCCCAGGTTCAAGGGATTATCCTGTTTCAGCCTCCTGAATAGC CTGCAACCTCCGCCTCCCAGCCTCCCAGGTTCGAGGGATTATCCTGTTTCAGCCTCCTGAATAGC A G PRXL2A Ensembl:ENSG00000122378 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1467879168 Functional Loss SNV dbSNP153 33..33 33 - - - 45083 RMVar_ID_45083 Human_SNP_ID_439396942 A-to-I Human chr10 + 80432379 80432379 80432379 AATTGACTGCCAGGCTGGGTGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGT AATTGACTGCCAGGCTGGGTGCAGTGGCTCACTCCTGTAATCCCAGCACTTTGGGAGGCCAAGGT A T PRXL2A Ensembl:ENSG00000122378 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270524973 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_383613,Human_RBP_ID_8172990,Human_RBP_ID_27407525 Human_miRNA_ID_1737369 45084 RMVar_ID_45084 Human_SNP_ID_439396960 A-to-I Human chr10 + 80432457 80432457 80432457 GAGGTCGGGAGTTCGAGACCAGCCTGAGCAACATGGCGAAACCCCGTCTCTACTAAAAATACAAA GAGGTCGGGAGTTCGAGACCAGCCTGAGCAACGTGGCGAAACCCCGTCTCTACTAAAAATACAAA A G PRXL2A Ensembl:ENSG00000122378 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1230795136 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_383614 45085 RMVar_ID_45085 Human_SNP_ID_439396967 A-to-I Human chr10 + 80432476 80432476 80432476 CAGCCTGAGCAACATGGCGAAACCCCGTCTCTACTAAAAATACAAAAATCACCCGGGTGTGGTGG CAGCCTGAGCAACATGGCGAAACCCCGTCTCTGCTAAAAATACAAAAATCACCCGGGTGTGGTGG A G PRXL2A Ensembl:ENSG00000122378 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1004983140 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_383614 Human_miRNA_ID_1219640 45086 RMVar_ID_45086 Human_SNP_ID_439396977 A-to-I Human chr10 + 80432510 80432510 80432510 TAAAAATACAAAAATCACCCGGGTGTGGTGGCAGGCACCTGTAGTCCCAGCTACCCGGGAGGCTG TAAAAATACAAAAATCACCCGGGTGTGGTGGCCGGCACCTGTAGTCCCAGCTACCCGGGAGGCTG A C PRXL2A Ensembl:ENSG00000122378 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1055854720 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_383615 45087 RMVar_ID_45087 Human_SNP_ID_439396995 A-to-I Human chr10 + 80432591 80432591 80432591 TGAACCTGGGAGGTGGAGGTTGCGGTGAGCTGAGATCACACCACTGTATTCCAGCCTGGGTGACT TGAACCTGGGAGGTGGAGGTTGCGGTGAGCTGCGATCACACCACTGTATTCCAGCCTGGGTGACT A C PRXL2A Ensembl:ENSG00000122378 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1007083088 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23473013 45088 RMVar_ID_45088 Human_SNP_ID_439396996 A-to-I Human chr10 + 80432591 80432591 80432591 TGAACCTGGGAGGTGGAGGTTGCGGTGAGCTGAGATCACACCACTGTATTCCAGCCTGGGTGACT TGAACCTGGGAGGTGGAGGTTGCGGTGAGCTGGGATCACACCACTGTATTCCAGCCTGGGTGACT A G PRXL2A Ensembl:ENSG00000122378 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1007083088 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23473013 45089 RMVar_ID_45089 Human_SNP_ID_439397004 A-to-I Human chr10 + 80432632 80432630 80432633 CACTGTATTCCAGCCTGGGTGACTGAGACTCTAACTAAAAAAAAAAAAAAAAAAAAATTGATTGC CACTGTATTCCAGCCTGGGTGACTGAGACTC___CTAAAAAAAAAAAAAAAAAAAAATTGATTGC CTAA C PRXL2A Ensembl:ENSG00000122378 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs772449573 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_23473013 45090 RMVar_ID_45090 Human_SNP_ID_439397007 A-to-I Human chr10 + 80432632 80432632 80432632 CACTGTATTCCAGCCTGGGTGACTGAGACTCTAACTAAAAAAAAAAAAAAAAAAAAATTGATTGC CACTGTATTCCAGCCTGGGTGACTGAGACTCTTACTAAAAAAAAAAAAAAAAAAAAATTGATTGC A T PRXL2A Ensembl:ENSG00000122378 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1430936019 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23473013 45091 RMVar_ID_45091 Human_SNP_ID_439397525 A-to-I Human chr10 + 80435093 80435092 80435093 AAAGTTAGCCTGTTGTGGTGGCGCGCACCTGTAATCCCAGCTACTCGGGTGGCTGAGGCAGGAGA AAAGTTAGCCTGTTGTGGTGGCGCGCACCTGT_ATCCCAGCTACTCGGGTGGCTGAGGCAGGAGA TA T PRXL2A Ensembl:ENSG00000122378 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs959673155 Functional Loss DEL dbSNP153 33..33 33 - - - 45092 RMVar_ID_45092 Human_SNP_ID_439397683 A-to-I Human chr10 + 80435711 80435711 80435711 GCCCAGGCTGGTCTCAAACTCCTGGCCTCCCAAAGTGTTTAGATTACAGGTGTAAGCCACCACAC GCCCAGGCTGGTCTCAAACTCCTGGCCTCCCAGAGTGTTTAGATTACAGGTGTAAGCCACCACAC A G PRXL2A Ensembl:ENSG00000122378 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs922262094 Functional Loss SNV dbSNP153 33..33 33 - - - 45093 RMVar_ID_45093 Human_SNP_ID_439397840 A-to-I Human chr10 + 80436326 80436326 80436326 TTGTAGAGGCAAGCTCTTATACTATCTTGCACAGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTC TTGTAGAGGCAAGCTCTTATACTATCTTGCACGGGCTGGTCTCGAACTCCTGGGCTCAAGCAGTC A G PRXL2A Ensembl:ENSG00000122378 Protein coding 3'UTR GSE38233;GSE100210;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 24183664,29129909,30559470 RNA-Seq:(High) rs957466225 Functional Loss SNV dbSNP153 33..33 33 - - - 45094 RMVar_ID_45094 Human_SNP_ID_439407258 A-to-I Human chr10 + 80475384 80475384 80475384 AGCCAGGGGTTTGAGATTAGCCTGGGCAACATAGTGAAACCCTATTTCTACAAAAAATTAAAAAA AGCCAGGGGTTTGAGATTAGCCTGGGCAACATGGTGAAACCCTATTTCTACAAAAAATTAAAAAA A G TSPAN14 Ensembl:ENSG00000108219 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1357499370 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24213,RMVar_hsa_circ_105595,RMVar_hsa_circ_144606,RMVar_hsa_circ_304498,RMVar_hsa_circ_274345,RMVar_hsa_circ_321874,RMVar_hsa_circ_144607,RMVar_hsa_circ_336459,RMVar_hsa_circ_272415,RMVar_hsa_circ_144608,RMVar_hsa_circ_144609,RMVar_hsa_circ_144610 45095 RMVar_ID_45095 Human_SNP_ID_439409008 A-to-I Human chr10 + 80481893 80481893 80481893 CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCACCTGCCACCATGCCCGGCTAATTGTT CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTGCAGGCACCTGCCACCATGCCCGGCTAATTGTT A G TSPAN14 Ensembl:ENSG00000108219 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1265617150 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24213,RMVar_hsa_circ_105595,RMVar_hsa_circ_144606,RMVar_hsa_circ_304498,RMVar_hsa_circ_274345,RMVar_hsa_circ_321874,RMVar_hsa_circ_144607,RMVar_hsa_circ_336459,RMVar_hsa_circ_272415,RMVar_hsa_circ_144608,RMVar_hsa_circ_144609,RMVar_hsa_circ_144610 45096 RMVar_ID_45096 Human_SNP_ID_439770727 A-to-I Human chr10 + 81912321 81912321 81912321 ATAGCTCACCGTAGCCTGAAACTGCTGGGCTGAAGTGATCCTCCTGCCTCAGCCTCCTGAGTAGC ATAGCTCACCGTAGCCTGAAACTGCTGGGCTGGAGTGATCCTCCTGCCTCAGCCTCCTGAGTAGC A G NRG3 Ensembl:ENSG00000185737 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank;ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1226634184 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27653,RMVar_hsa_circ_144621 45097 RMVar_ID_45097 Human_SNP_ID_439781758 A-to-I Human chr10 + 81958629 81958629 81958629 ATATAACACATAAACAGATATACAGGCTGGGCATGGTGGCTCATGCCTGTAATCCCGCCGAGGTG ATATAACACATAAACAGATATACAGGCTGGGCCTGGTGGCTCATGCCTGTAATCCCGCCGAGGTG A C NRG3 Ensembl:ENSG00000185737 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1288058809 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27653 45098 RMVar_ID_45098 Human_SNP_ID_439792312 A-to-I Human chr10 + 82001380 82001380 82001380 TAAAAATTAGCTGGGTTTTGTGGTGGGCATCCATAATCCCCGCTACTTGGGAGGCTGAGGCAGGA TAAAAATTAGCTGGGTTTTGTGGTGGGCATCCGTAATCCCCGCTACTTGGGAGGCTGAGGCAGGA A G NRG3 Ensembl:ENSG00000185737 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1473413283 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27653 45099 RMVar_ID_45099 Human_SNP_ID_439795979 A-to-I Human chr10 + 82015691 82015691 82015691 ACATGTGAGTCAATTAAACCTCTTTCCTTTATAAATTACCGCATCTCGGGCAGTTCTTTATAGCA ACATGTGAGTCAATTAAACCTCTTTCCTTTATGAATTACCGCATCTCGGGCAGTTCTTTATAGCA A G NRG3 Ensembl:ENSG00000185737 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1040299973 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27653 45100 RMVar_ID_45100 Human_SNP_ID_439813032 A-to-I Human chr10 + 82083026 82083025 82083027 CAGTGGTACAATCATAGCTCACACTGTCTCTCAAATTCCTGGACTCAAGCGATCCTCCCTCCATA CAGTGGTACAATCATAGCTCACACTGTCTCTC__ATTCCTGGACTCAAGCGATCCTCCCTCCATA CAA C NRG3 Ensembl:ENSG00000185737 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1375369489 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_27653 45101 RMVar_ID_45101 Human_SNP_ID_439816294 A-to-I Human chr10 + 82096441 82096441 82096441 GAGGTTGCAGTGAGCCGAGATTGCACTCCTGCACTCCAGCCTGGTGACAGAGCGAGAGTCTCAAA GAGGTTGCAGTGAGCCGAGATTGCACTCCTGCCCTCCAGCCTGGTGACAGAGCGAGAGTCTCAAA A C NRG3 Ensembl:ENSG00000185737 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1403676213 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27653 45102 RMVar_ID_45102 Human_SNP_ID_439824429 A-to-I Human chr10 + 82129042 82129042 82129042 TCAAGCGATTCTCCTGTCTCAGCCTCGCAAGTAGCTGTGATTACAGATGCCTGCCACCATGCCCA TCAAGCGATTCTCCTGTCTCAGCCTCGCAAGTGGCTGTGATTACAGATGCCTGCCACCATGCCCA A G NRG3 Ensembl:ENSG00000185737 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1415800083 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27653 45103 RMVar_ID_45103 Human_SNP_ID_439885559 A-to-I Human chr10 + 82372733 82372733 82372733 CTCCTGCCTCAGCCTCCCACCTAGCTGAGATTACAGGCATGCACCACCATGCTCAGCTAATTGTA CTCCTGCCTCAGCCTCCCACCTAGCTGAGATTGCAGGCATGCACCACCATGCTCAGCTAATTGTA A G NRG3 Ensembl:ENSG00000185737 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs957460891 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_344791 45104 RMVar_ID_45104 Human_SNP_ID_439916748 A-to-I Human chr10 + 82497838 82497838 82497838 AGGAGCACTCATACTGCTTTTTCATAATGGCTATACCAGTTCTCCCCACCAACGATAGACAAGGG AGGAGCACTCATACTGCTTTTTCATAATGGCTGTACCAGTTCTCCCCACCAACGATAGACAAGGG A G NRG3 Ensembl:ENSG00000185737 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs554759031 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_344791 45105 RMVar_ID_45105 Human_SNP_ID_440034686 A-to-I Human chr10 + 82977438 82977438 82977438 TGAGACCAGCCTGGCCAACATGGTGAAACCTCATCTCTACTAAAAATACAAAAATTAGCCTGCCA TGAGACCAGCCTGGCCAACATGGTGAAACCTCGTCTCTACTAAAAATACAAAAATTAGCCTGCCA A G NRG3 Ensembl:ENSG00000185737 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs368694060 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5793,RMVar_hsa_circ_267768,RMVar_hsa_circ_345711,RMVar_hsa_circ_144643,RMVar_hsa_circ_144642,RMVar_hsa_circ_52312,RMVar_hsa_circ_144646,RMVar_hsa_circ_144647 45106 RMVar_ID_45106 Human_SNP_ID_440034688 A-to-I Human chr10 + 82977444 82977441 82977444 CAGCCTGGCCAACATGGTGAAACCTCATCTCTACTAAAAATACAAAAATTAGCCTGCCATTGTGG CAGCCTGGCCAACATGGTGAAACCTCATCT___CTAAAAATACAAAAATTAGCCTGCCATTGTGG TCTA T NRG3 Ensembl:ENSG00000185737 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1000311583 Functional Loss DEL dbSNP153 31..33 33 - - - RMVar_hsa_circ_5793,RMVar_hsa_circ_267768,RMVar_hsa_circ_345711,RMVar_hsa_circ_144643,RMVar_hsa_circ_144642,RMVar_hsa_circ_52312,RMVar_hsa_circ_144646,RMVar_hsa_circ_144647 45107 RMVar_ID_45107 Human_SNP_ID_440034724 A-to-I Human chr10 + 82977541 82977541 82977541 TGGGGCAGGCGAATCACTTGAACCTGGGAGGTAGAGGTTGCAGTGAGCCAAGATCGTGCCACTGC TGGGGCAGGCGAATCACTTGAACCTGGGAGGTCGAGGTTGCAGTGAGCCAAGATCGTGCCACTGC A C NRG3 Ensembl:ENSG00000185737 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1486751444 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5793,RMVar_hsa_circ_267768,RMVar_hsa_circ_345711,RMVar_hsa_circ_144643,RMVar_hsa_circ_144642,RMVar_hsa_circ_52312,RMVar_hsa_circ_144646,RMVar_hsa_circ_144647 45108 RMVar_ID_45108 Human_SNP_ID_440333665 A-to-I Human chr10 + 84162902 84162902 84162902 AGGTCTGACAAGAGCTCCGAAGCCAGCTACCTAGAGACTTCATCTGCATAATAAGAACCTTGGTC AGGTCTGACAAGAGCTCCGAAGCCAGCTACCTGGAGACTTCATCTGCATAATAAGAACCTTGGTC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1262178296 Functional Loss SNV dbSNP153 33..33 33 - - - 45109 RMVar_ID_45109 Human_SNP_ID_440392064 A-to-I Human chr10 + 84381807 84381807 84381807 AAAATAAGCCGAGTGTGGTGGCACGTGCCTGTAGTCCCAGCTACTCGGGAGGCTAGGAGAATTGC AAAATAAGCCGAGTGTGGTGGCACGTGCCTGTTGTCCCAGCTACTCGGGAGGCTAGGAGAATTGC A T CCSER2 Ensembl:ENSG00000107771 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs555974837 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_144656,RMVar_hsa_circ_4535,RMVar_hsa_circ_286212,RMVar_hsa_circ_361919,RMVar_hsa_circ_93302,RMVar_hsa_circ_144654,RMVar_hsa_circ_144658,RMVar_hsa_circ_144655,RMVar_hsa_circ_144657 45110 RMVar_ID_45110 Human_SNP_ID_440394490 A-to-I Human chr10 - 84391854 84391854 84391854 GCATCACAAAAAAATATAAAATCTTGGATTACACTACTGGGATTCACAATGATCATGGTACAAAT GCATCACAAAAAAATATAAAATCTTGGATTACGCTACTGGGATTCACAATGATCATGGTACAAAT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs905770838 Functional Loss SNV dbSNP153 33..33 33 - - - 45111 RMVar_ID_45111 Human_SNP_ID_440405697 A-to-I Human chr10 + 84437453 84437453 84437453 GGAGAATCGCTTGAACTCCGGAGGCAGAGGTTACAATGAGCCAAGATCGTACCATTGCGCTCCAG GGAGAATCGCTTGAACTCCGGAGGCAGAGGTTGCAATGAGCCAAGATCGTACCATTGCGCTCCAG A G CCSER2 Ensembl:ENSG00000107771 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1226425162 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_144656,RMVar_hsa_circ_361919,RMVar_hsa_circ_93302,RMVar_hsa_circ_144655,RMVar_hsa_circ_5225,RMVar_hsa_circ_272301,RMVar_hsa_circ_314219,RMVar_hsa_circ_275434,RMVar_hsa_circ_23828,RMVar_hsa_circ_144664,RMVar_hsa_circ_144665,RMVar_hsa_circ_144663,RMVar_hsa_circ_282960,RMVar_hsa_circ_57924,RMVar_hsa_circ_144667,RMVar_hsa_circ_144668 45112 RMVar_ID_45112 Human_SNP_ID_440405818 A-to-I Human chr10 + 84437852 84437852 84437852 CTCCTGCATTAGCCTCCTAAGTAACTAGGATTACAGGCACGTGCCACCATGCTGGGGTAATTTTT CTCCTGCATTAGCCTCCTAAGTAACTAGGATTGCAGGCACGTGCCACCATGCTGGGGTAATTTTT A G CCSER2 Ensembl:ENSG00000107771 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1043161184 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17559097 RMVar_hsa_circ_144656,RMVar_hsa_circ_361919,RMVar_hsa_circ_93302,RMVar_hsa_circ_144655,RMVar_hsa_circ_5225,RMVar_hsa_circ_272301,RMVar_hsa_circ_314219,RMVar_hsa_circ_275434,RMVar_hsa_circ_23828,RMVar_hsa_circ_144664,RMVar_hsa_circ_144665,RMVar_hsa_circ_144663,RMVar_hsa_circ_282960,RMVar_hsa_circ_57924,RMVar_hsa_circ_144667,RMVar_hsa_circ_144668 45113 RMVar_ID_45113 Human_SNP_ID_440422808 A-to-I Human chr10 + 84502631 84502631 84502631 CTGACCTTGTGATCTACCTGGCTGGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCACG CTGACCTTGTGATCTACCTGGCTGGGCCTCCCGAAGTGCTGGGATTACAGGCGTGAGCCACCACG A G CCSER2 Ensembl:ENSG00000107771 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1209336732 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93302,RMVar_hsa_circ_144655 45114 RMVar_ID_45114 Human_SNP_ID_440792669 A-to-I Human chr10 - 85961403 85961403 85961403 TGGCGGGAGGCCTCCTCACTGGTCTGGGCTTCACTGTGCTTATGATACCAGGGTCCCTGGTGGGC TGGCGGGAGGCCTCCTCACTGGTCTGGGCTTCCCTGTGCTTATGATACCAGGGTCCCTGGTGGGC T G GRID1 Ensembl:ENSG00000182771 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs978146786 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2250,RMVar_hsa_circ_332771,RMVar_hsa_circ_144680,RMVar_hsa_circ_107919 45115 RMVar_ID_45115 Human_SNP_ID_440905983 A-to-I Human chr10 - 86437121 86437121 86437121 GTGCAAAGGCAGCTTAGCTACTGAGGTAGCGAATGTTCTGAGGACATTCTAGACAACAGCTTAGT GTGCAAAGGCAGCTTAGCTACTGAGGTAGCGAGTGTTCTGAGGACATTCTAGACAACAGCTTAGT T C WAPL Ensembl:ENSG00000062650 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1166186396 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11444355,Human_RBP_ID_23474065 Human_miRNA_ID_390826,Human_miRNA_ID_396824,Human_miRNA_ID_402901,Human_miRNA_ID_408873,Human_miRNA_ID_1712960,Human_miRNA_ID_2879622 RMVar_hsa_circ_85531,RMVar_hsa_circ_144685 45116 RMVar_ID_45116 Human_SNP_ID_440907226 A-to-I Human chr10 - 86442094 86442094 86442094 TGAATCCTGGAGGCGGAGTTTGCAGTGAGCCAAGATCGTGCCACTGCACTTCAGCCTGGGCTTCA TGAATCCTGGAGGCGGAGTTTGCAGTGAGCCATGATCGTGCCACTGCACTTCAGCCTGGGCTTCA T A WAPL Ensembl:ENSG00000062650 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251788801 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85531,RMVar_hsa_circ_55062,RMVar_hsa_circ_64301,RMVar_hsa_circ_144685 45117 RMVar_ID_45117 Human_SNP_ID_440907249 A-to-I Human chr10 - 86442169 86442169 86442169 AAATTTGCTGGGCGTGGCGGTGCACACCTCTAATCTCAGCTACTCGGGAGGCTGAGACGCAAGAA AAATTTGCTGGGCGTGGCGGTGCACACCTCTAGTCTCAGCTACTCGGGAGGCTGAGACGCAAGAA T C WAPL Ensembl:ENSG00000062650 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903929707 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85531,RMVar_hsa_circ_55062,RMVar_hsa_circ_64301,RMVar_hsa_circ_144685 45118 RMVar_ID_45118 Human_SNP_ID_440907250 A-to-I Human chr10 - 86442169 86442169 86442169 AAATTTGCTGGGCGTGGCGGTGCACACCTCTAATCTCAGCTACTCGGGAGGCTGAGACGCAAGAA AAATTTGCTGGGCGTGGCGGTGCACACCTCTACTCTCAGCTACTCGGGAGGCTGAGACGCAAGAA T G WAPL Ensembl:ENSG00000062650 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903929707 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85531,RMVar_hsa_circ_55062,RMVar_hsa_circ_64301,RMVar_hsa_circ_144685 45119 RMVar_ID_45119 Human_SNP_ID_440908663 A-to-I Human chr10 - 86447885 86447885 86447885 CGCCACCACGCCTGGCTAATTTTTGTATTTTTAGTAGAGGTGGTTTCACTGTGTTTGCCGGGCTA CGCCACCACGCCTGGCTAATTTTTGTATTTTTGGTAGAGGTGGTTTCACTGTGTTTGCCGGGCTA T C WAPL Ensembl:ENSG00000062650 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs764223434 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11444496 RMVar_hsa_circ_60122,RMVar_hsa_circ_85531,RMVar_hsa_circ_267851,RMVar_hsa_circ_55062,RMVar_hsa_circ_144685,RMVar_hsa_circ_302127,RMVar_hsa_circ_322056,RMVar_hsa_circ_144687,RMVar_hsa_circ_69793,RMVar_hsa_circ_102173,RMVar_hsa_circ_65852,RMVar_hsa_circ_329408,RMVar_hsa_circ_357918,RMVar_hsa_circ_144686,RMVar_hsa_circ_305977,RMVar_hsa_circ_144688,RMVar_hsa_circ_144689 45120 RMVar_ID_45120 Human_SNP_ID_440908664 A-to-I Human chr10 - 86447885 86447885 86447885 CGCCACCACGCCTGGCTAATTTTTGTATTTTTAGTAGAGGTGGTTTCACTGTGTTTGCCGGGCTA CGCCACCACGCCTGGCTAATTTTTGTATTTTTCGTAGAGGTGGTTTCACTGTGTTTGCCGGGCTA T G WAPL Ensembl:ENSG00000062650 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs764223434 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11444496 RMVar_hsa_circ_60122,RMVar_hsa_circ_85531,RMVar_hsa_circ_267851,RMVar_hsa_circ_55062,RMVar_hsa_circ_144685,RMVar_hsa_circ_302127,RMVar_hsa_circ_322056,RMVar_hsa_circ_144687,RMVar_hsa_circ_69793,RMVar_hsa_circ_102173,RMVar_hsa_circ_65852,RMVar_hsa_circ_329408,RMVar_hsa_circ_357918,RMVar_hsa_circ_144686,RMVar_hsa_circ_305977,RMVar_hsa_circ_144688,RMVar_hsa_circ_144689 45121 RMVar_ID_45121 Human_SNP_ID_440908786 A-to-I Human chr10 - 86448391 86448391 86448391 GCTGAAGTACAGTGGTCCAGTCACAGCTCACTACAGCCTTTACCTCCCAGGCTCAGGTGATCCTT GCTGAAGTACAGTGGTCCAGTCACAGCTCACTGCAGCCTTTACCTCCCAGGCTCAGGTGATCCTT T C WAPL Ensembl:ENSG00000062650 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1233298629 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60122,RMVar_hsa_circ_85531,RMVar_hsa_circ_267851,RMVar_hsa_circ_55062,RMVar_hsa_circ_144685,RMVar_hsa_circ_302127,RMVar_hsa_circ_322056,RMVar_hsa_circ_144687,RMVar_hsa_circ_69793,RMVar_hsa_circ_102173,RMVar_hsa_circ_65852,RMVar_hsa_circ_329408,RMVar_hsa_circ_357918,RMVar_hsa_circ_144686,RMVar_hsa_circ_305977,RMVar_hsa_circ_144688,RMVar_hsa_circ_144689 45122 RMVar_ID_45122 Human_SNP_ID_440913078 A-to-I Human chr10 - 86464585 86464585 86464585 TGATCTGTCCTCCTCGGCCTTCCTGGGATTACAGACATGAGCCACTACGCCTGTCCAAAACATGT TGATCTGTCCTCCTCGGCCTTCCTGGGATTACGGACATGAGCCACTACGCCTGTCCAAAACATGT T C WAPL Ensembl:ENSG00000062650 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs751173889 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37954,RMVar_hsa_circ_267851,RMVar_hsa_circ_55062,RMVar_hsa_circ_302127,RMVar_hsa_circ_144687,RMVar_hsa_circ_69793,RMVar_hsa_circ_102173,RMVar_hsa_circ_329408,RMVar_hsa_circ_144686,RMVar_hsa_circ_109267,RMVar_hsa_circ_144689,RMVar_hsa_circ_352490,RMVar_hsa_circ_274487,RMVar_hsa_circ_70741,RMVar_hsa_circ_324331,RMVar_hsa_circ_144690,RMVar_hsa_circ_72754,RMVar_hsa_circ_144696,RMVar_hsa_circ_144697,RMVar_hsa_circ_110961,RMVar_hsa_circ_25717,RMVar_hsa_circ_51925,RMVar_hsa_circ_144698,RMVar_hsa_circ_292823,RMVar_hsa_circ_282473,RMVar_hsa_circ_349417,RMVar_hsa_circ_144699,RMVar_hsa_circ_321301,RMVar_hsa_circ_2221,RMVar_hsa_circ_144702 45123 RMVar_ID_45123 Human_SNP_ID_440913251 A-to-I Human chr10 - 86465303 86465303 86465303 TACTTGGGAGTCTGAGACATGAGAATCGCCTGAACCTGGAACCTAGGAGGCGAGGCGGAGGTTTC TACTTGGGAGTCTGAGACATGAGAATCGCCTGTACCTGGAACCTAGGAGGCGAGGCGGAGGTTTC T A WAPL Ensembl:ENSG00000062650 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs999535822 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11444804 RMVar_hsa_circ_37954,RMVar_hsa_circ_267851,RMVar_hsa_circ_55062,RMVar_hsa_circ_302127,RMVar_hsa_circ_144687,RMVar_hsa_circ_69793,RMVar_hsa_circ_102173,RMVar_hsa_circ_329408,RMVar_hsa_circ_144686,RMVar_hsa_circ_109267,RMVar_hsa_circ_144689,RMVar_hsa_circ_352490,RMVar_hsa_circ_274487,RMVar_hsa_circ_70741,RMVar_hsa_circ_324331,RMVar_hsa_circ_144690,RMVar_hsa_circ_72754,RMVar_hsa_circ_144696,RMVar_hsa_circ_144697,RMVar_hsa_circ_110961,RMVar_hsa_circ_25717,RMVar_hsa_circ_51925,RMVar_hsa_circ_144698,RMVar_hsa_circ_292823,RMVar_hsa_circ_282473,RMVar_hsa_circ_349417,RMVar_hsa_circ_144699,RMVar_hsa_circ_321301,RMVar_hsa_circ_2221,RMVar_hsa_circ_144702 45124 RMVar_ID_45124 Human_SNP_ID_440913276 A-to-I Human chr10 - 86465385 86465385 86465385 TCTGGCCAATATGGTGAAACCCCATCTCCACTAAAAATACAAAAATTAGCTGTGCGTGGTGGTGG TCTGGCCAATATGGTGAAACCCCATCTCCACTGAAAATACAAAAATTAGCTGTGCGTGGTGGTGG T C WAPL Ensembl:ENSG00000062650 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1002913395 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37954,RMVar_hsa_circ_267851,RMVar_hsa_circ_55062,RMVar_hsa_circ_302127,RMVar_hsa_circ_144687,RMVar_hsa_circ_69793,RMVar_hsa_circ_102173,RMVar_hsa_circ_329408,RMVar_hsa_circ_144686,RMVar_hsa_circ_109267,RMVar_hsa_circ_144689,RMVar_hsa_circ_352490,RMVar_hsa_circ_274487,RMVar_hsa_circ_70741,RMVar_hsa_circ_324331,RMVar_hsa_circ_144690,RMVar_hsa_circ_72754,RMVar_hsa_circ_144696,RMVar_hsa_circ_144697,RMVar_hsa_circ_110961,RMVar_hsa_circ_25717,RMVar_hsa_circ_51925,RMVar_hsa_circ_144698,RMVar_hsa_circ_292823,RMVar_hsa_circ_282473,RMVar_hsa_circ_349417,RMVar_hsa_circ_144699,RMVar_hsa_circ_321301,RMVar_hsa_circ_2221,RMVar_hsa_circ_144702 45125 RMVar_ID_45125 Human_SNP_ID_440914327 A-to-I Human chr10 - 86469390 86469390 86469390 AAATTACTCGGGCGTGGTGGTGCTTGCCTGTAATCCCAGCCACTCAGGAGGCTGAGGCACAAGAA AAATTACTCGGGCGTGGTGGTGCTTGCCTGTAGTCCCAGCCACTCAGGAGGCTGAGGCACAAGAA T C WAPL Ensembl:ENSG00000062650 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs150593975 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37954,RMVar_hsa_circ_267851,RMVar_hsa_circ_55062,RMVar_hsa_circ_302127,RMVar_hsa_circ_144687,RMVar_hsa_circ_102173,RMVar_hsa_circ_329408,RMVar_hsa_circ_144686,RMVar_hsa_circ_109267,RMVar_hsa_circ_144689,RMVar_hsa_circ_352490,RMVar_hsa_circ_274487,RMVar_hsa_circ_70741,RMVar_hsa_circ_144690,RMVar_hsa_circ_72754,RMVar_hsa_circ_144697,RMVar_hsa_circ_110961,RMVar_hsa_circ_8670,RMVar_hsa_circ_25717,RMVar_hsa_circ_51925,RMVar_hsa_circ_144698,RMVar_hsa_circ_292823,RMVar_hsa_circ_282473,RMVar_hsa_circ_144699,RMVar_hsa_circ_295584,RMVar_hsa_circ_321301,RMVar_hsa_circ_2221,RMVar_hsa_circ_144702,RMVar_hsa_circ_349945,RMVar_hsa_circ_356921,RMVar_hsa_circ_358268,RMVar_hsa_circ_62216,RMVar_hsa_circ_266605,RMVar_hsa_circ_43209,RMVar_hsa_circ_144703 45126 RMVar_ID_45126 Human_SNP_ID_440914336 A-to-I Human chr10 - 86469433 86469433 86469433 CCTGGGCAACATGGTGAAACCCCATCTCTACTAAAAATGCAAAAAATTACTCGGGCGTGGTGGTG CCTGGGCAACATGGTGAAACCCCATCTCTACTGAAAATGCAAAAAATTACTCGGGCGTGGTGGTG T C WAPL Ensembl:ENSG00000062650 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1423450064 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37954,RMVar_hsa_circ_267851,RMVar_hsa_circ_55062,RMVar_hsa_circ_302127,RMVar_hsa_circ_144687,RMVar_hsa_circ_102173,RMVar_hsa_circ_329408,RMVar_hsa_circ_144686,RMVar_hsa_circ_109267,RMVar_hsa_circ_144689,RMVar_hsa_circ_352490,RMVar_hsa_circ_274487,RMVar_hsa_circ_70741,RMVar_hsa_circ_144690,RMVar_hsa_circ_72754,RMVar_hsa_circ_144697,RMVar_hsa_circ_110961,RMVar_hsa_circ_8670,RMVar_hsa_circ_25717,RMVar_hsa_circ_51925,RMVar_hsa_circ_144698,RMVar_hsa_circ_292823,RMVar_hsa_circ_282473,RMVar_hsa_circ_144699,RMVar_hsa_circ_295584,RMVar_hsa_circ_321301,RMVar_hsa_circ_2221,RMVar_hsa_circ_144702,RMVar_hsa_circ_349945,RMVar_hsa_circ_356921,RMVar_hsa_circ_358268,RMVar_hsa_circ_62216,RMVar_hsa_circ_266605,RMVar_hsa_circ_43209,RMVar_hsa_circ_144703 45127 RMVar_ID_45127 Human_SNP_ID_440916558 A-to-I Human chr10 - 86478892 86478892 86478892 TGGGGTTTCACTATGTTGGACAGCCTGGTCTCAAACTCCTGACCTCAAGTGGTCTGCCCACCTCG TGGGGTTTCACTATGTTGGACAGCCTGGTCTCGAACTCCTGACCTCAAGTGGTCTGCCCACCTCG T C WAPL Ensembl:ENSG00000062650 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1012924691 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24839217 RMVar_hsa_circ_37954,RMVar_hsa_circ_267851,RMVar_hsa_circ_55062,RMVar_hsa_circ_352490,RMVar_hsa_circ_70741,RMVar_hsa_circ_72754,RMVar_hsa_circ_51925,RMVar_hsa_circ_356921,RMVar_hsa_circ_358268,RMVar_hsa_circ_62216,RMVar_hsa_circ_43209,RMVar_hsa_circ_92276,RMVar_hsa_circ_352846,RMVar_hsa_circ_52597,RMVar_hsa_circ_332986,RMVar_hsa_circ_144706,RMVar_hsa_circ_61157,RMVar_hsa_circ_144707,RMVar_hsa_circ_367231 45128 RMVar_ID_45128 Human_SNP_ID_440916566 A-to-I Human chr10 - 86478929 86478929 86478929 CCACACCCGGCTAATTTTTTTGTATTTTTAGTAGAGATGGGGTTTCACTATGTTGGACAGCCTGG CCACACCCGGCTAATTTTTTTGTATTTTTAGTGGAGATGGGGTTTCACTATGTTGGACAGCCTGG T C WAPL Ensembl:ENSG00000062650 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1276711168 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37954,RMVar_hsa_circ_267851,RMVar_hsa_circ_55062,RMVar_hsa_circ_352490,RMVar_hsa_circ_70741,RMVar_hsa_circ_72754,RMVar_hsa_circ_51925,RMVar_hsa_circ_356921,RMVar_hsa_circ_358268,RMVar_hsa_circ_62216,RMVar_hsa_circ_43209,RMVar_hsa_circ_92276,RMVar_hsa_circ_352846,RMVar_hsa_circ_52597,RMVar_hsa_circ_332986,RMVar_hsa_circ_144706,RMVar_hsa_circ_61157,RMVar_hsa_circ_144707,RMVar_hsa_circ_367231 45129 RMVar_ID_45129 Human_SNP_ID_440916572 A-to-I Human chr10 - 86478949 86478949 86478949 GGAATTACAGATGTGTGCCACCACACCCGGCTAATTTTTTTGTATTTTTAGTAGAGATGGGGTTT GGAATTACAGATGTGTGCCACCACACCCGGCTGATTTTTTTGTATTTTTAGTAGAGATGGGGTTT T C WAPL Ensembl:ENSG00000062650 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1305969138 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37954,RMVar_hsa_circ_267851,RMVar_hsa_circ_55062,RMVar_hsa_circ_352490,RMVar_hsa_circ_70741,RMVar_hsa_circ_72754,RMVar_hsa_circ_51925,RMVar_hsa_circ_356921,RMVar_hsa_circ_358268,RMVar_hsa_circ_62216,RMVar_hsa_circ_43209,RMVar_hsa_circ_92276,RMVar_hsa_circ_352846,RMVar_hsa_circ_52597,RMVar_hsa_circ_332986,RMVar_hsa_circ_144706,RMVar_hsa_circ_61157,RMVar_hsa_circ_144707,RMVar_hsa_circ_367231 45130 RMVar_ID_45130 Human_SNP_ID_440917957 A-to-I Human chr10 - 86484339 86484339 86484339 AGGTGGACATCACCACACCCTGGTGATCTTGTATTTTTTGTAGAGGTGGGGTTTCACCATGTTGT AGGTGGACATCACCACACCCTGGTGATCTTGTTTTTTTTGTAGAGGTGGGGTTTCACCATGTTGT T A WAPL Ensembl:ENSG00000062650 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1439272928 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37954,RMVar_hsa_circ_267851,RMVar_hsa_circ_55062,RMVar_hsa_circ_352490,RMVar_hsa_circ_70741,RMVar_hsa_circ_72754,RMVar_hsa_circ_51925,RMVar_hsa_circ_356921,RMVar_hsa_circ_358268,RMVar_hsa_circ_62216,RMVar_hsa_circ_43209,RMVar_hsa_circ_92276,RMVar_hsa_circ_352846,RMVar_hsa_circ_52597,RMVar_hsa_circ_332986,RMVar_hsa_circ_144706,RMVar_hsa_circ_61157,RMVar_hsa_circ_144707,RMVar_hsa_circ_367231 45131 RMVar_ID_45131 Human_SNP_ID_440919368 A-to-I Human chr10 - 86490057 86490057 86490057 GACGTGCACCACCATGCCCGGCTAATTTTTGTATTTCTAGTAGATATGGGGTTTCACCTGTTTGC GACGTGCACCACCATGCCCGGCTAATTTTTGTGTTTCTAGTAGATATGGGGTTTCACCTGTTTGC T C WAPL Ensembl:ENSG00000062650 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1190044768 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2234587,Human_RBP_ID_11445468 RMVar_hsa_circ_37954,RMVar_hsa_circ_267851,RMVar_hsa_circ_55062,RMVar_hsa_circ_352490,RMVar_hsa_circ_70741,RMVar_hsa_circ_72754,RMVar_hsa_circ_51925,RMVar_hsa_circ_356921,RMVar_hsa_circ_358268,RMVar_hsa_circ_62216,RMVar_hsa_circ_43209,RMVar_hsa_circ_92276,RMVar_hsa_circ_352846,RMVar_hsa_circ_52597,RMVar_hsa_circ_332986,RMVar_hsa_circ_144706,RMVar_hsa_circ_61157,RMVar_hsa_circ_144707,RMVar_hsa_circ_367231 45132 RMVar_ID_45132 Human_SNP_ID_440919557 A-to-I Human chr10 - 86490806 86490806 86490806 CACCTGCCTCGGCCTCCCAAAGTGCTGGAATTACAGGTGTGAGCCACCGCGCCCGGCCTTCAAAT CACCTGCCTCGGCCTCCCAAAGTGCTGGAATTGCAGGTGTGAGCCACCGCGCCCGGCCTTCAAAT T C WAPL Ensembl:ENSG00000062650 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1283668239 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37954,RMVar_hsa_circ_267851,RMVar_hsa_circ_55062,RMVar_hsa_circ_352490,RMVar_hsa_circ_70741,RMVar_hsa_circ_72754,RMVar_hsa_circ_51925,RMVar_hsa_circ_356921,RMVar_hsa_circ_358268,RMVar_hsa_circ_62216,RMVar_hsa_circ_43209,RMVar_hsa_circ_92276,RMVar_hsa_circ_352846,RMVar_hsa_circ_52597,RMVar_hsa_circ_332986,RMVar_hsa_circ_144706,RMVar_hsa_circ_61157,RMVar_hsa_circ_144707,RMVar_hsa_circ_367231 45133 RMVar_ID_45133 Human_SNP_ID_440919728 A-to-I Human chr10 - 86491304 86491304 86491304 AAATCCCGTTTCTACTAAAAACACAAAAAATTAGCCATGTGTGGTGGCGGGCGCCTGTGGTCCCA AAATCCCGTTTCTACTAAAAACACAAAAAATTGGCCATGTGTGGTGGCGGGCGCCTGTGGTCCCA T C WAPL Ensembl:ENSG00000062650 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs868443872 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37954,RMVar_hsa_circ_267851,RMVar_hsa_circ_55062,RMVar_hsa_circ_352490,RMVar_hsa_circ_70741,RMVar_hsa_circ_72754,RMVar_hsa_circ_51925,RMVar_hsa_circ_356921,RMVar_hsa_circ_358268,RMVar_hsa_circ_62216,RMVar_hsa_circ_43209,RMVar_hsa_circ_92276,RMVar_hsa_circ_352846,RMVar_hsa_circ_52597,RMVar_hsa_circ_332986,RMVar_hsa_circ_144706,RMVar_hsa_circ_61157,RMVar_hsa_circ_144707,RMVar_hsa_circ_367231 45134 RMVar_ID_45134 Human_SNP_ID_440920131 A-to-I Human chr10 - 86492868 86492868 86492868 TATTTTTGGTAGAGACGGGGTTTCACAGTGTTAGCCAGGATGGTCTCTATCTCCTGACCCTCGTG TATTTTTGGTAGAGACGGGGTTTCACAGTGTTGGCCAGGATGGTCTCTATCTCCTGACCCTCGTG T C WAPL Ensembl:ENSG00000062650 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs971923378 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24839355 RMVar_hsa_circ_37954,RMVar_hsa_circ_267851,RMVar_hsa_circ_55062,RMVar_hsa_circ_352490,RMVar_hsa_circ_70741,RMVar_hsa_circ_72754,RMVar_hsa_circ_51925,RMVar_hsa_circ_356921,RMVar_hsa_circ_358268,RMVar_hsa_circ_62216,RMVar_hsa_circ_43209,RMVar_hsa_circ_92276,RMVar_hsa_circ_352846,RMVar_hsa_circ_52597,RMVar_hsa_circ_332986,RMVar_hsa_circ_144706,RMVar_hsa_circ_61157,RMVar_hsa_circ_144707,RMVar_hsa_circ_367231 45135 RMVar_ID_45135 Human_SNP_ID_440923439 A-to-I Human chr10 - 86506036 86506033 86506036 AGAGACAAGGTCTTGAACTCCTGAGCTCAAGTAGTCCTCACACCTTGGCCTCCCAAAGTGTTGGT AGAGACAAGGTCTTGAACTCCTGAGCTCAAGT___CCTCACACCTTGGCCTCCCAAAGTGTTGGT GACT G WAPL Ensembl:ENSG00000062650 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1290229868 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_11445935 RMVar_hsa_circ_70741,RMVar_hsa_circ_356921,RMVar_hsa_circ_352846,RMVar_hsa_circ_332986,RMVar_hsa_circ_144707,RMVar_hsa_circ_61056,RMVar_hsa_circ_366037 45136 RMVar_ID_45136 Human_SNP_ID_440923616 A-to-I Human chr10 - 86506668 86506668 86506668 CTCCTACCCCCACTTCCTGAGTAGCTAGGACTATAGGAACGTGCCACCACTCCTGGCTGATTTTC CTCCTACCCCCACTTCCTGAGTAGCTAGGACTGTAGGAACGTGCCACCACTCCTGGCTGATTTTC T C WAPL Ensembl:ENSG00000062650 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1047948459 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70741,RMVar_hsa_circ_356921,RMVar_hsa_circ_352846,RMVar_hsa_circ_332986,RMVar_hsa_circ_144707,RMVar_hsa_circ_61056,RMVar_hsa_circ_366037 45137 RMVar_ID_45137 Human_SNP_ID_440990685 A-to-I Human chr10 + 86766126 86766125 86766127 CTCCCATCTCAGCCTCCTGAATAGCTGGGACCAGAGGTGCATGCTACCATGCCCAGCTAATTAAA CTCCCATCTCAGCCTCCTGAATAGCTGGGACC__AGGTGCATGCTACCATGCCCAGCTAATTAAA CAG C BMPR1A Ensembl:ENSG00000107779 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs951691147 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_110474,RMVar_hsa_circ_127063,RMVar_hsa_circ_144708,RMVar_hsa_circ_144709 45138 RMVar_ID_45138 Human_SNP_ID_440993626 A-to-I Human chr10 + 86777351 86777351 86777351 CTGTAATCCCAGCACTTTGGGAAGGCCCAGACAGGAGGATTACTTGAACCCAGGAGTTTGAGATC CTGTAATCCCAGCACTTTGGGAAGGCCCAGACGGGAGGATTACTTGAACCCAGGAGTTTGAGATC A G BMPR1A Ensembl:ENSG00000107779 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1370192196 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17559102 RMVar_hsa_circ_110474,RMVar_hsa_circ_127063,RMVar_hsa_circ_144708,RMVar_hsa_circ_144709 45139 RMVar_ID_45139 Human_SNP_ID_441009892 A-to-I Human chr10 + 86839787 86839783 86839788 TCAAGCGATCCTTCTGCCTCAGTCTCCCACATAGCTGGGACTACAGGCACACATCACCATGCCCA TCAAGCGATCCTTCTGCCTCAGTCTCCCA_____CTGGGACTACAGGCACACATCACCATGCCCA ACATAG A BMPR1A Ensembl:ENSG00000107779 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1385841692 Functional Loss DEL dbSNP153 30..34 33 - - - Human_RBP_ID_17559104 RMVar_hsa_circ_110474,RMVar_hsa_circ_127063,RMVar_hsa_circ_3442,RMVar_hsa_circ_360456,RMVar_hsa_circ_144708,RMVar_hsa_circ_144709,RMVar_hsa_circ_369548,RMVar_hsa_circ_276412,RMVar_hsa_circ_314400,RMVar_hsa_circ_46647,RMVar_hsa_circ_144712,RMVar_hsa_circ_2459,RMVar_hsa_circ_144711 45140 RMVar_ID_45140 Human_SNP_ID_441014459 A-to-I Human chr10 + 86859389 86859389 86859389 TGGGGTCTCACTACATTGCCCAGGCTGGTCTCAAACTCCTGGGCTCAAGTGATCCTCCTGCCTTG TGGGGTCTCACTACATTGCCCAGGCTGGTCTCCAACTCCTGGGCTCAAGTGATCCTCCTGCCTTG A C BMPR1A Ensembl:ENSG00000107779 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1038550987 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110474,RMVar_hsa_circ_127063,RMVar_hsa_circ_3442,RMVar_hsa_circ_360456,RMVar_hsa_circ_144708,RMVar_hsa_circ_144709,RMVar_hsa_circ_369548,RMVar_hsa_circ_276412,RMVar_hsa_circ_314400,RMVar_hsa_circ_46647,RMVar_hsa_circ_144712,RMVar_hsa_circ_2459,RMVar_hsa_circ_144711 45141 RMVar_ID_45141 Human_SNP_ID_441014520 A-to-I Human chr10 + 86859600 86859600 86859600 CCAGCACTTTGGAAGGCTGAGGCAGGTGGATCACCTGAGGTCAGGAGTTCGAGACCAGCCTGGCC CCAGCACTTTGGAAGGCTGAGGCAGGTGGATCCCCTGAGGTCAGGAGTTCGAGACCAGCCTGGCC A C BMPR1A Ensembl:ENSG00000107779 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs962880531 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110474,RMVar_hsa_circ_127063,RMVar_hsa_circ_3442,RMVar_hsa_circ_360456,RMVar_hsa_circ_144708,RMVar_hsa_circ_144709,RMVar_hsa_circ_369548,RMVar_hsa_circ_276412,RMVar_hsa_circ_314400,RMVar_hsa_circ_46647,RMVar_hsa_circ_144712,RMVar_hsa_circ_2459,RMVar_hsa_circ_144711 45142 RMVar_ID_45142 Human_SNP_ID_441036006 A-to-I Human chr10 - 86941764 86941764 86941764 GATGGGTCTCACTTTGTCGTCCAGGCTTGAGTACAGTGGTGGGATCATGGCTCACTGCAGCCTAG GATGGGTCTCACTTTGTCGTCCAGGCTTGAGTGCAGTGGTGGGATCATGGCTCACTGCAGCCTAG T C MMRN2 Ensembl:ENSG00000173269 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1427713136 Functional Loss SNV dbSNP153 33..33 33 - - - 45143 RMVar_ID_45143 Human_SNP_ID_441061981 A-to-I Human chr10 - 87041935 87041935 87041935 CCGAGATCACACCACTGCACTCCACCTTGAGCAACAGACTGAGACTCTGTCTCAAAAAAAAAAAA CCGAGATCACACCACTGCACTCCACCTTGAGCGACAGACTGAGACTCTGTCTCAAAAAAAAAAAA T C lnc-GLUD1-1 RNACentral:URS00008B32C3 lincRNA intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1262841042 Functional Loss SNV dbSNP153 33..33 33 - - - 45144 RMVar_ID_45144 Human_SNP_ID_441075831 A-to-I Human chr10 + 87096519 87096519 87096519 GCCTGTAATCCCAGCACTTTGGGGGCCAAAGCAGGCTGATCGCTTGAGGCCAGGAGTTCAAGACC GCCTGTAATCCCAGCACTTTGGGGGCCAAAGCTGGCTGATCGCTTGAGGCCAGGAGTTCAAGACC A T SHLD2 Ensembl:ENSG00000122376 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs937381412 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107189,RMVar_hsa_circ_144742 45145 RMVar_ID_45145 Human_SNP_ID_441076074 A-to-I Human chr10 + 87097552 87097552 87097552 GGAGAGAGGTTGCAGTGAGCCGAGATCGTGCCATTGCACTCCAGCCTGGGCAACAGAGCGAGTCT GGAGAGAGGTTGCAGTGAGCCGAGATCGTGCCGTTGCACTCCAGCCTGGGCAACAGAGCGAGTCT A G SHLD2 Ensembl:ENSG00000122376 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1358819773 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17559109,Human_RBP_ID_22708583,Human_RBP_ID_26775334 RMVar_hsa_circ_7600,RMVar_hsa_circ_107189,RMVar_hsa_circ_376242,RMVar_hsa_circ_144742,RMVar_hsa_circ_348612,RMVar_hsa_circ_144743 45146 RMVar_ID_45146 Human_SNP_ID_441076422 A-to-I Human chr10 + 87098875 87098875 87098875 ACAGTTTACCACAGCCTGGACTTCCTGGGCTCAGGCAATCCTCCCACCTCAGCCTCCTGAGTAGC ACAGTTTACCACAGCCTGGACTTCCTGGGCTCGGGCAATCCTCCCACCTCAGCCTCCTGAGTAGC A G SHLD2 Ensembl:ENSG00000122376 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1430562034 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7600,RMVar_hsa_circ_107189,RMVar_hsa_circ_376242,RMVar_hsa_circ_144742,RMVar_hsa_circ_348612,RMVar_hsa_circ_144743 45147 RMVar_ID_45147 Human_SNP_ID_441076423 A-to-I Human chr10 + 87098879 87098879 87098879 TTTACCACAGCCTGGACTTCCTGGGCTCAGGCAATCCTCCCACCTCAGCCTCCTGAGTAGCTAGG TTTACCACAGCCTGGACTTCCTGGGCTCAGGCGATCCTCCCACCTCAGCCTCCTGAGTAGCTAGG A G SHLD2 Ensembl:ENSG00000122376 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs955705468 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7600,RMVar_hsa_circ_107189,RMVar_hsa_circ_376242,RMVar_hsa_circ_144742,RMVar_hsa_circ_348612,RMVar_hsa_circ_144743 45148 RMVar_ID_45148 Human_SNP_ID_441076457 A-to-I Human chr10 + 87099010 87099010 87099010 GTTGCCCAGGCTGGTCTCGAACTCCTGGGCTCAAGCGATATGCCCGCCTCTGCCTCCCACAGTGC GTTGCCCAGGCTGGTCTCGAACTCCTGGGCTCGAGCGATATGCCCGCCTCTGCCTCCCACAGTGC A G SHLD2 Ensembl:ENSG00000122376 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs969103798 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7600,RMVar_hsa_circ_107189,RMVar_hsa_circ_376242,RMVar_hsa_circ_144742,RMVar_hsa_circ_348612,RMVar_hsa_circ_144743 45149 RMVar_ID_45149 Human_SNP_ID_441076847 A-to-I Human chr10 + 87100683 87100683 87100683 TATTTTCAGTAGAGATGGGGTTTTATCATGTTAGTCAGGCTGATCTCGAACTCCTTGACCCAGGT TATTTTCAGTAGAGATGGGGTTTTATCATGTTCGTCAGGCTGATCTCGAACTCCTTGACCCAGGT A C SHLD2 Ensembl:ENSG00000122376 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs540061534 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11449121,Human_RBP_ID_24840409 RMVar_hsa_circ_7600,RMVar_hsa_circ_107189,RMVar_hsa_circ_376242,RMVar_hsa_circ_144742,RMVar_hsa_circ_348612,RMVar_hsa_circ_144743 45150 RMVar_ID_45150 Human_SNP_ID_441077770 A-to-I Human chr10 + 87104680 87104680 87104680 GTACTAAGGTAGGATTCTTTTTTTTTTTCTTGAGACGGAGTCTTGCTCTGTCGCCCAGGCTGGAG GTACTAAGGTAGGATTCTTTTTTTTTTTCTTGTGACGGAGTCTTGCTCTGTCGCCCAGGCTGGAG A T SHLD2 Ensembl:ENSG00000122376 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1279203961 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7600,RMVar_hsa_circ_107189,RMVar_hsa_circ_376242,RMVar_hsa_circ_144742,RMVar_hsa_circ_348612,RMVar_hsa_circ_144743 45151 RMVar_ID_45151 Human_SNP_ID_441077822 A-to-I Human chr10 + 87104841 87104841 87104841 TGCCACCACGCCCGCCTAATTTTTGTACTTTCAGTAGAGATGAGGTTTCACCATGTTGGCCAGGC TGCCACCACGCCCGCCTAATTTTTGTACTTTCCGTAGAGATGAGGTTTCACCATGTTGGCCAGGC A C SHLD2 Ensembl:ENSG00000122376 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs367641534 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7600,RMVar_hsa_circ_107189,RMVar_hsa_circ_376242,RMVar_hsa_circ_144742,RMVar_hsa_circ_348612,RMVar_hsa_circ_144743 45152 RMVar_ID_45152 Human_SNP_ID_441077828 A-to-I Human chr10 + 87104870 87104870 87104870 TTCAGTAGAGATGAGGTTTCACCATGTTGGCCAGGCTGCTCTTGAACTCCTGACCTTGTGATCCG TTCAGTAGAGATGAGGTTTCACCATGTTGGCCGGGCTGCTCTTGAACTCCTGACCTTGTGATCCG A G SHLD2 Ensembl:ENSG00000122376 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1440616496 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7600,RMVar_hsa_circ_107189,RMVar_hsa_circ_376242,RMVar_hsa_circ_144742,RMVar_hsa_circ_348612,RMVar_hsa_circ_144743 45153 RMVar_ID_45153 Human_SNP_ID_441085784 A-to-I Human chr10 + 87141404 87141404 87141404 TCTTGTTGCCCATTGCTGGAGTGCAATGGCATAGTCTCGGCTCACTGCAACCTCCACCTCCTGGA TCTTGTTGCCCATTGCTGGAGTGCAATGGCATGGTCTCGGCTCACTGCAACCTCCACCTCCTGGA A G SHLD2 Ensembl:ENSG00000122376 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1003082896 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7600,RMVar_hsa_circ_107189,RMVar_hsa_circ_376242,RMVar_hsa_circ_144742,RMVar_hsa_circ_348612,RMVar_hsa_circ_144743 45154 RMVar_ID_45154 Human_SNP_ID_441087916 A-to-I Human chr10 + 87149959 87149959 87149959 TTTGTAGAGATGGTGGTCTTACTATGTTGTCCAAGCTGGCCTCGAACTCCTGGTCTCAAGTGATC TTTGTAGAGATGGTGGTCTTACTATGTTGTCCCAGCTGGCCTCGAACTCCTGGTCTCAAGTGATC A C SHLD2 Ensembl:ENSG00000122376 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1454000435 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7600,RMVar_hsa_circ_107189,RMVar_hsa_circ_376242,RMVar_hsa_circ_144742,RMVar_hsa_circ_348612,RMVar_hsa_circ_144743 45155 RMVar_ID_45155 Human_SNP_ID_441100552 A-to-I Human chr10 - 87208466 87208466 87208466 TGTGCCTGGGCCGGGTGCGGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCCAAGGCCAGT TGTGCCTGGGCCGGGTGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCCAGT T C NUTM2A-AS1 Ensembl:ENSG00000223482 lincRNA intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1422401268 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1157714,Human_Splice_Rec_1157724,Human_Splice_Rec_1157736 45156 RMVar_ID_45156 Human_SNP_ID_441101474 A-to-I Human chr10 - 87212516 87212516 87212516 GTCGCCCAGGCTGGAGTGCGGTGGCGCGATCTAGGCTTACTGCAAGCTCCACCTCCCGGGTTTAC GTCGCCCAGGCTGGAGTGCGGTGGCGCGATCTCGGCTTACTGCAAGCTCCACCTCCCGGGTTTAC T G NUTM2A-AS1 Ensembl:ENSG00000223482 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1328789690 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8245481 45157 RMVar_ID_45157 Human_SNP_ID_441102239 A-to-I Human chr10 - 87215190 87215190 87215190 AAGAGGTTGGCTGGGTGCAGTGGCTCACGCCTATAATCCTAGCACTTTGGGAGACCGAGAGGGGT AAGAGGTTGGCTGGGTGCAGTGGCTCACGCCTGTAATCCTAGCACTTTGGGAGACCGAGAGGGGT T C NUTM2A-AS1,AL157893.1 Ensembl:ENSG00000223482,Ensembl:ENSG00000285257 lincRNA,Pseudogene intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1438098846 Functional Loss SNV dbSNP153 33..33 33 - - - 45158 RMVar_ID_45158 Human_SNP_ID_441108588 A-to-I Human chr10 - 87241209 87241209 87241209 TGAGGCCCTCAACAGAAGCAGATGCTGGTGCCATGCTTCTCGTACAGCCTGCAGAATTGTGTGAG TGAGGCCCTCAACAGAAGCAGATGCTGGTGCCTTGCTTCTCGTACAGCCTGCAGAATTGTGTGAG T A NUTM2A-AS1 Ensembl:ENSG00000223482 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1370882045 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1157735 45159 RMVar_ID_45159 Human_SNP_ID_441109851 A-to-I Human chr10 - 87246153 87246153 87246153 TCACTGTAGCCTCGAAATTCTGGGCCGAAATGATCCGCCTGCCTCAGCCTCCAAAGTAGCTGAGA TCACTGTAGCCTCGAAATTCTGGGCCGAAATGGTCCGCCTGCCTCAGCCTCCAAAGTAGCTGAGA T C NUTM2A-AS1 Ensembl:ENSG00000223482 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs974664203 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1077302 Human_Splice_Rec_1157692,Human_Splice_Rec_1157693,Human_Splice_Rec_1157702,Human_Splice_Rec_1157703,Human_Splice_Rec_1157732,Human_Splice_Rec_1157733,Human_Splice_Rec_1157740,Human_Splice_Rec_1157741,Human_Splice_Rec_1157750,Human_Splice_Rec_1157751,Human_Splice_Rec_1157760,Human_Splice_Rec_1157761,Human_Splice_Rec_1157770,Human_Splice_Rec_1157771,Human_Splice_Rec_1157788,Human_Splice_Rec_1157789,Human_Splice_Rec_1157800,Human_Splice_Rec_1157801 Human_miRNA_ID_3191889,Human_miRNA_ID_3212075 45160 RMVar_ID_45160 Human_SNP_ID_441110430 A-to-I Human chr10 - 87248456 87248456 87248456 GGAGTGCAGTGGCATGATCTTGGCTCACTGCAACCTCCGCCTCCCAAGTTCAAGCAGTTCTCATG GGAGTGCAGTGGCATGATCTTGGCTCACTGCAGCCTCCGCCTCCCAAGTTCAAGCAGTTCTCATG T C NUTM2A-AS1 Ensembl:ENSG00000223482 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1471462635 Functional Loss SNV dbSNP153 33..33 33 - - - 45161 RMVar_ID_45161 Human_SNP_ID_441114082 A-to-I Human chr10 - 87261885 87261885 87261885 CCAGGCTGGCCTTGAACTCCTGGATTGAAGCGATCCTCCCGCCTTGGCCTCCCAAAGTGTCAATT CCAGGCTGGCCTTGAACTCCTGGATTGAAGCGGTCCTCCCGCCTTGGCCTCCCAAAGTGTCAATT T C NUTM2A-AS1 Ensembl:ENSG00000223482 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs960256808 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8246097,Human_RBP_ID_11449671 45162 RMVar_ID_45162 Human_SNP_ID_441218796 A-to-I Human chr10 + 87741245 87741245 87741245 ATCATAACAATGTTCTTTCTAGATGGTGATGGAAAGTGGGGACTGGCTGGTTGGTGGAGACCTTC ATCATAACAATGTTCTTTCTAGATGGTGATGGCAAGTGGGGACTGGCTGGTTGGTGGAGACCTTC A C PAPSS2 Ensembl:ENSG00000198682 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1307569722 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1158100,Human_Splice_Rec_1158124 RMVar_hsa_circ_54580,RMVar_hsa_circ_360680,RMVar_hsa_circ_72048,RMVar_hsa_circ_144757,RMVar_hsa_circ_320380,RMVar_hsa_circ_345498,RMVar_hsa_circ_144758 45163 RMVar_ID_45163 Human_SNP_ID_441223414 A-to-I Human chr10 - 87760646 87760646 87760646 TAGCTCACTGCAGCCTTGAACTCCTTGGCTCAAGTGATCCTCCTGCCTCAACCTCCTGAGTAGCT TAGCTCACTGCAGCCTTGAACTCCTTGGCTCAGGTGATCCTCCTGCCTCAACCTCCTGAGTAGCT T C ATAD1 Ensembl:ENSG00000138138 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1274492778 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4618,RMVar_hsa_circ_301808,RMVar_hsa_circ_41529,RMVar_hsa_circ_298709,RMVar_hsa_circ_144761,RMVar_hsa_circ_144760 45164 RMVar_ID_45164 Human_SNP_ID_441223592 A-to-I Human chr10 - 87761460 87761460 87761460 ATGGGGTTTCGCCATGTTGCCCAGGCTGGTCTAGAACTCCTGAGCTCAAGAGATCCACCCATCTC ATGGGGTTTCGCCATGTTGCCCAGGCTGGTCTGGAACTCCTGAGCTCAAGAGATCCACCCATCTC T C ATAD1 Ensembl:ENSG00000138138 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1269601666 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24841180 RMVar_hsa_circ_4618,RMVar_hsa_circ_301808,RMVar_hsa_circ_41529,RMVar_hsa_circ_298709,RMVar_hsa_circ_144761,RMVar_hsa_circ_144760 45165 RMVar_ID_45165 Human_SNP_ID_441223593 A-to-I Human chr10 - 87761460 87761460 87761460 ATGGGGTTTCGCCATGTTGCCCAGGCTGGTCTAGAACTCCTGAGCTCAAGAGATCCACCCATCTC ATGGGGTTTCGCCATGTTGCCCAGGCTGGTCTCGAACTCCTGAGCTCAAGAGATCCACCCATCTC T G ATAD1 Ensembl:ENSG00000138138 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1269601666 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24841180 RMVar_hsa_circ_4618,RMVar_hsa_circ_301808,RMVar_hsa_circ_41529,RMVar_hsa_circ_298709,RMVar_hsa_circ_144761,RMVar_hsa_circ_144760 45166 RMVar_ID_45166 Human_SNP_ID_441223631 A-to-I Human chr10 - 87761654 87761648 87761654 TATTTTTCATGGCTACAGGGAATTTTTTTTTTAGACAATCTCTGCTTTGTCACCCAGGCTAGAGT TATTTTTCATGGCTACAGGGAATTTTTTTTTT______TCTCTGCTTTGTCACCCAGGCTAGAGT ATTGTCT A ATAD1 Ensembl:ENSG00000138138 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1293779384 Functional Loss DEL dbSNP153 33..38 33 - - - Human_RBP_ID_11450804 RMVar_hsa_circ_4618,RMVar_hsa_circ_301808,RMVar_hsa_circ_41529,RMVar_hsa_circ_298709,RMVar_hsa_circ_144761,RMVar_hsa_circ_144760 45167 RMVar_ID_45167 Human_SNP_ID_441223674 A-to-I Human chr10 - 87761803 87761803 87761803 TGGATGCACCACTGCATTCTAGCCTGGGTGACAGAGCAAGATCCTGTCTCTAAAAAAGAAATAAG TGGATGCACCACTGCATTCTAGCCTGGGTGACTGAGCAAGATCCTGTCTCTAAAAAAGAAATAAG T A ATAD1 Ensembl:ENSG00000138138 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs766154218 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24841184 RMVar_hsa_circ_4618,RMVar_hsa_circ_301808,RMVar_hsa_circ_41529,RMVar_hsa_circ_298709,RMVar_hsa_circ_144761,RMVar_hsa_circ_144760 45168 RMVar_ID_45168 Human_SNP_ID_441223684 A-to-I Human chr10 - 87761863 87761863 87761863 CTAGTTACTCGGGAGGCTGAGGCAGGAGGATCACTTGAGCTTAGAAGTTCAAGGCTGCAGTGGAT CTAGTTACTCGGGAGGCTGAGGCAGGAGGATCGCTTGAGCTTAGAAGTTCAAGGCTGCAGTGGAT T C ATAD1 Ensembl:ENSG00000138138 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs977029177 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4618,RMVar_hsa_circ_301808,RMVar_hsa_circ_41529,RMVar_hsa_circ_298709,RMVar_hsa_circ_144761,RMVar_hsa_circ_144760 45169 RMVar_ID_45169 Human_SNP_ID_441223849 A-to-I Human chr10 - 87762602 87762602 87762602 AAATTAGCTGGACATGGTGGCTGGCAACCGTAATCCTGGCTACTTGGGAGGCTGAGGCAGGAAAA AAATTAGCTGGACATGGTGGCTGGCAACCGTAGTCCTGGCTACTTGGGAGGCTGAGGCAGGAAAA T C ATAD1 Ensembl:ENSG00000138138 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1422614763 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4618,RMVar_hsa_circ_301808,RMVar_hsa_circ_41529,RMVar_hsa_circ_298709,RMVar_hsa_circ_144761,RMVar_hsa_circ_144760 45170 RMVar_ID_45170 Human_SNP_ID_441223850 A-to-I Human chr10 - 87762603 87762603 87762603 AAAATTAGCTGGACATGGTGGCTGGCAACCGTAATCCTGGCTACTTGGGAGGCTGAGGCAGGAAA AAAATTAGCTGGACATGGTGGCTGGCAACCGTGATCCTGGCTACTTGGGAGGCTGAGGCAGGAAA T C ATAD1 Ensembl:ENSG00000138138 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1364766971 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4618,RMVar_hsa_circ_301808,RMVar_hsa_circ_41529,RMVar_hsa_circ_298709,RMVar_hsa_circ_144761,RMVar_hsa_circ_144760 45171 RMVar_ID_45171 Human_SNP_ID_441223873 A-to-I Human chr10 - 87762671 87762671 87762671 CTGAGGTCAGGAGTTCGAAACCAGCCTGGCCAACATGGTGAAACCCTGTCTCTACTAAAAATACA CTGAGGTCAGGAGTTCGAAACCAGCCTGGCCAGCATGGTGAAACCCTGTCTCTACTAAAAATACA T C ATAD1 Ensembl:ENSG00000138138 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs972731092 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4618,RMVar_hsa_circ_301808,RMVar_hsa_circ_41529,RMVar_hsa_circ_298709,RMVar_hsa_circ_144761,RMVar_hsa_circ_144760 45172 RMVar_ID_45172 Human_SNP_ID_441223892 A-to-I Human chr10 - 87762740 87762740 87762740 TTTGATAACTGCTTTCAAAAAAACATTGTGTAATCCTGGCACTTTGGGAGGCCAAGGCAGGCAGA TTTGATAACTGCTTTCAAAAAAACATTGTGTAGTCCTGGCACTTTGGGAGGCCAAGGCAGGCAGA T C ATAD1 Ensembl:ENSG00000138138 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1204217674 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11450815 RMVar_hsa_circ_4618,RMVar_hsa_circ_301808,RMVar_hsa_circ_41529,RMVar_hsa_circ_298709,RMVar_hsa_circ_144761,RMVar_hsa_circ_144760 45173 RMVar_ID_45173 Human_SNP_ID_441224171 A-to-I Human chr10 - 87763659 87763659 87763659 CCCAGGCTGACGTGTTGTTTTTTTAGGGTCTCACTGTATTACCCAGGCTAAAGTGCTGTGATATG CCCAGGCTGACGTGTTGTTTTTTTAGGGTCTCGCTGTATTACCCAGGCTAAAGTGCTGTGATATG T C ATAD1 Ensembl:ENSG00000138138 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs533730948 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2235587,Human_RBP_ID_3359764,Human_RBP_ID_11450838 RMVar_hsa_circ_4618,RMVar_hsa_circ_301808,RMVar_hsa_circ_41529,RMVar_hsa_circ_298709,RMVar_hsa_circ_144761,RMVar_hsa_circ_144760 45174 RMVar_ID_45174 Human_SNP_ID_441236840 A-to-I Human chr10 - 87817937 87817937 87817937 TCGCCTTGGCGTCCGGCCCGGCCTGGGCCCTTAGGGTCTGCTTAGCTCTTCCCCAAGACTCGTGC TCGCCTTGGCGTCCGGCCCGGCCTGGGCCCTTTGGGTCTGCTTAGCTCTTCCCCAAGACTCGTGC T A ATAD1 Ensembl:ENSG00000138138 Protein coding 5'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs755889235 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4136909 45175 RMVar_ID_45175 Human_SNP_ID_441249917 A-to-I Human chr10 + 87871680 87871680 87871680 CCACGCCCGGCTAATTTTATATTTTTTTTTTCAGTAGAGATGGGGGGTTTCTCCATGTTGGTCAG CCACGCCCGGCTAATTTTATATTTTTTTTTTCGGTAGAGATGGGGGGTTTCTCCATGTTGGTCAG A G PTEN Ensembl:ENSG00000171862 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs887540848 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6010706 RMVar_hsa_circ_144775,RMVar_hsa_circ_377437 45176 RMVar_ID_45176 Human_SNP_ID_441250310 A-to-I Human chr10 + 87873124 87873124 87873124 CATAGGCAGACCCTGTCTCTACAAAAAAAAATACAAAAATTAGTCGGGTGTTATAGTGCGCATTG CATAGGCAGACCCTGTCTCTACAAAAAAAAATGCAAAAATTAGTCGGGTGTTATAGTGCGCATTG A G PTEN Ensembl:ENSG00000171862 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs922526429 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2235771 RMVar_hsa_circ_144775,RMVar_hsa_circ_377437 45177 RMVar_ID_45177 Human_SNP_ID_441250334 A-to-I Human chr10 + 87873197 87873197 87873197 AGCTACTGAGGAGGCTGAGGTGGGATCACCTGAGACTGGGACTTTGAGGCTGCATTGAGCTGTGA AGCTACTGAGGAGGCTGAGGTGGGATCACCTGCGACTGGGACTTTGAGGCTGCATTGAGCTGTGA A C PTEN Ensembl:ENSG00000171862 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1419230370 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6010751,Human_RBP_ID_11452308,Human_RBP_ID_17559116 RMVar_hsa_circ_144775,RMVar_hsa_circ_377437 45178 RMVar_ID_45178 Human_SNP_ID_441250336 A-to-I Human chr10 + 87873199 87873199 87873199 CTACTGAGGAGGCTGAGGTGGGATCACCTGAGACTGGGACTTTGAGGCTGCATTGAGCTGTGATT CTACTGAGGAGGCTGAGGTGGGATCACCTGAGGCTGGGACTTTGAGGCTGCATTGAGCTGTGATT A G PTEN Ensembl:ENSG00000171862 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1462937696 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6010751,Human_RBP_ID_11452308,Human_RBP_ID_17559116 RMVar_hsa_circ_144775,RMVar_hsa_circ_377437 45179 RMVar_ID_45179 Human_SNP_ID_441259172 A-to-I Human chr10 + 87908531 87908531 87908531 CAAGACCAGACTGGCTGGTATAGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCTGGTGT CAAGACCAGACTGGCTGGTATAGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCTGGTGT A G PTEN Ensembl:ENSG00000171862 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1472704222 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_144775,RMVar_hsa_circ_377437,RMVar_hsa_circ_340652,RMVar_hsa_circ_341380 45180 RMVar_ID_45180 Human_SNP_ID_441259175 A-to-I Human chr10 + 87908537 87908537 87908537 CAGACTGGCTGGTATAGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCTGGTGTGGTCGG CAGACTGGCTGGTATAGTGAAACCCCATCTCTGCTAAAAATACAAAAATTAGCTGGTGTGGTCGG A G PTEN Ensembl:ENSG00000171862 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1456780957 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_144775,RMVar_hsa_circ_377437,RMVar_hsa_circ_340652,RMVar_hsa_circ_341380 45181 RMVar_ID_45181 Human_SNP_ID_441259679 A-to-I Human chr10 + 87910627 87910627 87910627 TTTCGTATTTTTAGTAGAAACATGGTTTCACCATGTTGGCCAAGCTGGTCTCGAACTCTTGGCCT TTTCGTATTTTTAGTAGAAACATGGTTTCACCGTGTTGGCCAAGCTGGTCTCGAACTCTTGGCCT A G PTEN Ensembl:ENSG00000171862 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs950135578 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_144775,RMVar_hsa_circ_377437,RMVar_hsa_circ_340652,RMVar_hsa_circ_341380 45182 RMVar_ID_45182 Human_SNP_ID_441266862 A-to-I Human chr10 + 87940186 87940186 87940186 ATTTGCAGGGTTGGGCACGGTGGCTCATACCTATATTCCCAGCACTTTGGGAGACTCAAGCGGGA ATTTGCAGGGTTGGGCACGGTGGCTCATACCTGTATTCCCAGCACTTTGGGAGACTCAAGCGGGA A G PTEN Ensembl:ENSG00000171862 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs748325353 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_225474 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 45183 RMVar_ID_45183 Human_SNP_ID_441266891 A-to-I Human chr10 + 87940308 87940308 87940308 TCTACAAAAAAATATTTAAAAAATAGCCGGGCATGGTGTCACGTGCCTGTAGTTCCAGCTGCTTG TCTACAAAAAAATATTTAAAAAATAGCCGGGCGTGGTGTCACGTGCCTGTAGTTCCAGCTGCTTG A G PTEN Ensembl:ENSG00000171862 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1355116525 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1078099,Human_RBP_ID_11453506 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 45184 RMVar_ID_45184 Human_SNP_ID_441268212 A-to-I Human chr10 - 87946037 87946037 87946037 AAAACTTTTTATTACCCTTTTGGGTAGAAATGAGAATTTATTTGCCAGGAAGGATGATCCCATCA AAAACTTTTTATTACCCTTTTGGGTAGAAATGGGAATTTATTTGCCAGGAAGGATGATCCCATCA T C lnc-KLLN-1 RNACentral:URS00008BF54B lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs929885257 Functional Loss SNV dbSNP153 33..33 33 - - - 45185 RMVar_ID_45185 Human_SNP_ID_441268218 A-to-I Human chr10 - 87946056 87946056 87946056 TTTTTTAAACATTTCACTGAAAACTTTTTATTACCCTTTTGGGTAGAAATGAGAATTTATTTGCC TTTTTTAAACATTTCACTGAAAACTTTTTATTGCCCTTTTGGGTAGAAATGAGAATTTATTTGCC T C lnc-KLLN-1 RNACentral:URS00008BF54B lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1428170967 Functional Loss SNV dbSNP153 33..33 33 - - - 45186 RMVar_ID_45186 Human_SNP_ID_441274118 A-to-I Human chr10 + 87967922 87967922 87967922 ACTCTCCTTACTTTATTTCAGTTACCATCCCCATAGAATTTGACAAGAATTGCTATGACTGAAAG ACTCTCCTTACTTTATTTCAGTTACCATCCCCGTAGAATTTGACAAGAATTGCTATGACTGAAAG A G PTEN Ensembl:ENSG00000171862 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs998649990 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8763936,Human_RBP_ID_24457823 Human_miRNA_ID_841535,Human_miRNA_ID_1375228 45187 RMVar_ID_45187 Human_SNP_ID_441483709 A-to-I Human chr10 + 88886147 88886147 88886147 ATTGGAACACTTCTTAATAAAGAACTTAATAAAAAGCATTACTTACAAAATACCAAAACGTCAAG ATTGGAACACTTCTTAATAAAGAACTTAATAAGAAGCATTACTTACAAAATACCAAAACGTCAAG A G STAMBPL1 Ensembl:ENSG00000138134 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1258581916 Functional Loss SNV dbSNP153 33..33 33 - - - 45188 RMVar_ID_45188 Human_SNP_ID_441493116 A-to-I Human chr10 + 88927465 88927465 88927465 ATCAAAAGGCAGGCCTTCATTTGGACTGCTACAACAAAAATACCATAAACTGGGTGACGTAAACA ATCAAAAGGCAGGCCTTCATTTGGACTGCTACGACAAAAATACCATAAACTGGGTGACGTAAACA A G STAMBPL1 Ensembl:ENSG00000138134 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934216209 Functional Loss SNV dbSNP153 33..33 33 - - - 45189 RMVar_ID_45189 Human_SNP_ID_441497157 A-to-I Human chr10 + 88944233 88944233 88944233 CCAGCTCGGACACTTCTTAGTTGTGTGAGCTTAGGCAAGTTTTTAACCCTTCTCAGCTTCAGTCT CCAGCTCGGACACTTCTTAGTTGTGTGAGCTTGGGCAAGTTTTTAACCCTTCTCAGCTTCAGTCT A G STAMBPL1 Ensembl:ENSG00000138134 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1409119849 Functional Loss SNV dbSNP153 33..33 33 - - - 45190 RMVar_ID_45190 Human_SNP_ID_441588621 A-to-I Human chr10 - 89331615 89331614 89331616 AGCTCAAGCATCTGCCCTCCTCGGCCTCCCAAAGTGTTGGGCTTATGGGTGTGAGCCACTGCGGC AGCTCAAGCATCTGCCCTCCTCGGCCTCCCA__GTGTTGGGCTTATGGGTGTGAGCCACTGCGGC CTT C LIPA Ensembl:ENSG00000107798 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1183226600 Functional Loss DEL dbSNP153 32..33 33 - - - 45191 RMVar_ID_45191 Human_SNP_ID_441680320 A-to-I Human chr10 + 89720729 89720729 89720729 TATTTATTTATTTATTTATTTATTTTTGAGAGAGGGTCTTGCCCTGTTGCCCAGGCTAGAGTGCA TATTTATTTATTTATTTATTTATTTTTGAGAGCGGGTCTTGCCCTGTTGCCCAGGCTAGAGTGCA A C KIF20B Ensembl:ENSG00000138182 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1416755191 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11454860 RMVar_hsa_circ_23393,RMVar_hsa_circ_3562,RMVar_hsa_circ_144816,RMVar_hsa_circ_81412,RMVar_hsa_circ_355111,RMVar_hsa_circ_60465,RMVar_hsa_circ_360231,RMVar_hsa_circ_309707,RMVar_hsa_circ_44813,RMVar_hsa_circ_144817,RMVar_hsa_circ_144818,RMVar_hsa_circ_35626,RMVar_hsa_circ_343648,RMVar_hsa_circ_347467,RMVar_hsa_circ_317366,RMVar_hsa_circ_98388,RMVar_hsa_circ_144820,RMVar_hsa_circ_144819,RMVar_hsa_circ_282796,RMVar_hsa_circ_342668,RMVar_hsa_circ_144822,RMVar_hsa_circ_144823 45192 RMVar_ID_45192 Human_SNP_ID_441680520 A-to-I Human chr10 + 89721471 89721471 89721471 AGGTAGGAGGATTGCTTGAGCTCAGGAGTTCAAAACTAGCCTGGGCAACATAGTGAGACCCCATC AGGTAGGAGGATTGCTTGAGCTCAGGAGTTCACAACTAGCCTGGGCAACATAGTGAGACCCCATC A C KIF20B Ensembl:ENSG00000138182 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1183892468 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23393,RMVar_hsa_circ_3562,RMVar_hsa_circ_144816,RMVar_hsa_circ_81412,RMVar_hsa_circ_355111,RMVar_hsa_circ_60465,RMVar_hsa_circ_360231,RMVar_hsa_circ_309707,RMVar_hsa_circ_44813,RMVar_hsa_circ_144817,RMVar_hsa_circ_144818,RMVar_hsa_circ_35626,RMVar_hsa_circ_343648,RMVar_hsa_circ_347467,RMVar_hsa_circ_317366,RMVar_hsa_circ_98388,RMVar_hsa_circ_144820,RMVar_hsa_circ_144819,RMVar_hsa_circ_282796,RMVar_hsa_circ_342668,RMVar_hsa_circ_144822,RMVar_hsa_circ_144823 45193 RMVar_ID_45193 Human_SNP_ID_441680679 A-to-I Human chr10 + 89722116 89722116 89722116 AAAAATGTTTTGTAGACATGAGGCCTTGCTCTATTGCCCAGGCTGATCTTGAACCCTTGGGCTCA AAAAATGTTTTGTAGACATGAGGCCTTGCTCTGTTGCCCAGGCTGATCTTGAACCCTTGGGCTCA A G KIF20B Ensembl:ENSG00000138182 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1052214560 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6012310,Human_RBP_ID_11499565 RMVar_hsa_circ_23393,RMVar_hsa_circ_3562,RMVar_hsa_circ_144816,RMVar_hsa_circ_81412,RMVar_hsa_circ_355111,RMVar_hsa_circ_60465,RMVar_hsa_circ_360231,RMVar_hsa_circ_309707,RMVar_hsa_circ_44813,RMVar_hsa_circ_144817,RMVar_hsa_circ_144818,RMVar_hsa_circ_35626,RMVar_hsa_circ_343648,RMVar_hsa_circ_347467,RMVar_hsa_circ_317366,RMVar_hsa_circ_98388,RMVar_hsa_circ_144820,RMVar_hsa_circ_144819,RMVar_hsa_circ_282796,RMVar_hsa_circ_342668,RMVar_hsa_circ_144822,RMVar_hsa_circ_144823 45194 RMVar_ID_45194 Human_SNP_ID_441680764 A-to-I Human chr10 + 89722436 89722436 89722436 TCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGTGGATCATGAGGTTGAGAGATTAAG TCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGTGGATCATGAGGTTGAGAGATTAAG A G KIF20B Ensembl:ENSG00000138182 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1564661292 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23393,RMVar_hsa_circ_3562,RMVar_hsa_circ_144816,RMVar_hsa_circ_81412,RMVar_hsa_circ_355111,RMVar_hsa_circ_60465,RMVar_hsa_circ_360231,RMVar_hsa_circ_309707,RMVar_hsa_circ_44813,RMVar_hsa_circ_144817,RMVar_hsa_circ_144818,RMVar_hsa_circ_35626,RMVar_hsa_circ_343648,RMVar_hsa_circ_347467,RMVar_hsa_circ_317366,RMVar_hsa_circ_98388,RMVar_hsa_circ_144820,RMVar_hsa_circ_144819,RMVar_hsa_circ_282796,RMVar_hsa_circ_342668,RMVar_hsa_circ_144822,RMVar_hsa_circ_144823 45195 RMVar_ID_45195 Human_SNP_ID_441680915 A-to-I Human chr10 + 89723010 89723010 89723010 TGGTAGTACCATAATTAAACCAATCCTTTAACATTGGTTGAGTTGGGTTCACTTTTTCATTATTT TGGTAGTACCATAATTAAACCAATCCTTTAACGTTGGTTGAGTTGGGTTCACTTTTTCATTATTT A G KIF20B Ensembl:ENSG00000138182 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4934495 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5121,GWAS_ID_5122,GWAS_ID_5123,GWAS_ID_5124,GWAS_ID_5125,GWAS_ID_5126,GWAS_ID_5127,GWAS_ID_5128,GWAS_ID_5129,GWAS_ID_5130,GWAS_ID_5131,GWAS_ID_5132,GWAS_ID_5133,GWAS_ID_5134,GWAS_ID_5135,GWAS_ID_5136,GWAS_ID_5137,GWAS_ID_5138,GWAS_ID_5139,GWAS_ID_5140,GWAS_ID_5141,GWAS_ID_5142,GWAS_ID_5143,GWAS_ID_5144,GWAS_ID_5145,GWAS_ID_5146,GWAS_ID_5147,GWAS_ID_5148,GWAS_ID_5149,GWAS_ID_5150,GWAS_ID_5151,GWAS_ID_5152,GWAS_ID_5153,GWAS_ID_5154,GWAS_ID_5155,GWAS_ID_5156,GWAS_ID_5157,GWAS_ID_5158,GWAS_ID_5159,GWAS_ID_5160,GWAS_ID_5161,GWAS_ID_5162,GWAS_ID_5163,GWAS_ID_5164,GWAS_ID_5165,GWAS_ID_5166,GWAS_ID_5167,GWAS_ID_5168,GWAS_ID_5169,GWAS_ID_5170,GWAS_ID_5171,GWAS_ID_5172,GWAS_ID_5173,GWAS_ID_5174,GWAS_ID_5175,GWAS_ID_5176,GWAS_ID_5177,GWAS_ID_5178,GWAS_ID_5179,GWAS_ID_5180,GWAS_ID_5181,GWAS_ID_5182,GWAS_ID_5183,GWAS_ID_5184,GWAS_ID_5185,GWAS_ID_5186,GWAS_ID_5187,GWAS_ID_5188,GWAS_ID_5189,GWAS_ID_5190,GWAS_ID_5191,GWAS_ID_5192,GWAS_ID_5193,GWAS_ID_5194,GWAS_ID_5195,GWAS_ID_5196,GWAS_ID_5197,GWAS_ID_5198,GWAS_ID_5199,GWAS_ID_5200,GWAS_ID_5201,GWAS_ID_5202,GWAS_ID_5203,GWAS_ID_5204,GWAS_ID_5205,GWAS_ID_5206,GWAS_ID_5207,GWAS_ID_5208,GWAS_ID_5209,GWAS_ID_5210,GWAS_ID_5211,GWAS_ID_5212,GWAS_ID_5213,GWAS_ID_5214,GWAS_ID_5215,GWAS_ID_5216,GWAS_ID_5217,GWAS_ID_5218,GWAS_ID_5219,GWAS_ID_5220,GWAS_ID_5221,GWAS_ID_5222,GWAS_ID_5223,GWAS_ID_5224,GWAS_ID_5225,GWAS_ID_5226,GWAS_ID_5227,GWAS_ID_5228,GWAS_ID_5229,GWAS_ID_5230,GWAS_ID_5231,GWAS_ID_5232,GWAS_ID_5233,GWAS_ID_5234,GWAS_ID_5235,GWAS_ID_5236,GWAS_ID_5237,GWAS_ID_5238,GWAS_ID_5239,GWAS_ID_5240,GWAS_ID_5241,GWAS_ID_5242,GWAS_ID_5243,GWAS_ID_5244,GWAS_ID_5245,GWAS_ID_5246,GWAS_ID_5247,GWAS_ID_5248,GWAS_ID_5249,GWAS_ID_5250,GWAS_ID_5251,GWAS_ID_5252,GWAS_ID_5253,GWAS_ID_5254,GWAS_ID_5255,GWAS_ID_5256 RMVar_hsa_circ_23393,RMVar_hsa_circ_3562,RMVar_hsa_circ_144816,RMVar_hsa_circ_81412,RMVar_hsa_circ_355111,RMVar_hsa_circ_60465,RMVar_hsa_circ_360231,RMVar_hsa_circ_309707,RMVar_hsa_circ_44813,RMVar_hsa_circ_144817,RMVar_hsa_circ_144818,RMVar_hsa_circ_35626,RMVar_hsa_circ_343648,RMVar_hsa_circ_347467,RMVar_hsa_circ_317366,RMVar_hsa_circ_98388,RMVar_hsa_circ_144820,RMVar_hsa_circ_144819,RMVar_hsa_circ_282796,RMVar_hsa_circ_342668,RMVar_hsa_circ_144822,RMVar_hsa_circ_144823 45196 RMVar_ID_45196 Human_SNP_ID_441680916 A-to-I Human chr10 + 89723010 89723010 89723010 TGGTAGTACCATAATTAAACCAATCCTTTAACATTGGTTGAGTTGGGTTCACTTTTTCATTATTT TGGTAGTACCATAATTAAACCAATCCTTTAACTTTGGTTGAGTTGGGTTCACTTTTTCATTATTT A T KIF20B Ensembl:ENSG00000138182 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4934495 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5121,GWAS_ID_5122,GWAS_ID_5123,GWAS_ID_5124,GWAS_ID_5125,GWAS_ID_5126,GWAS_ID_5127,GWAS_ID_5128,GWAS_ID_5129,GWAS_ID_5130,GWAS_ID_5131,GWAS_ID_5132,GWAS_ID_5133,GWAS_ID_5134,GWAS_ID_5135,GWAS_ID_5136,GWAS_ID_5137,GWAS_ID_5138,GWAS_ID_5139,GWAS_ID_5140,GWAS_ID_5141,GWAS_ID_5142,GWAS_ID_5143,GWAS_ID_5144,GWAS_ID_5145,GWAS_ID_5146,GWAS_ID_5147,GWAS_ID_5148,GWAS_ID_5149,GWAS_ID_5150,GWAS_ID_5151,GWAS_ID_5152,GWAS_ID_5153,GWAS_ID_5154,GWAS_ID_5155,GWAS_ID_5156,GWAS_ID_5157,GWAS_ID_5158,GWAS_ID_5159,GWAS_ID_5160,GWAS_ID_5161,GWAS_ID_5162,GWAS_ID_5163,GWAS_ID_5164,GWAS_ID_5165,GWAS_ID_5166,GWAS_ID_5167,GWAS_ID_5168,GWAS_ID_5169,GWAS_ID_5170,GWAS_ID_5171,GWAS_ID_5172,GWAS_ID_5173,GWAS_ID_5174,GWAS_ID_5175,GWAS_ID_5176,GWAS_ID_5177,GWAS_ID_5178,GWAS_ID_5179,GWAS_ID_5180,GWAS_ID_5181,GWAS_ID_5182,GWAS_ID_5183,GWAS_ID_5184,GWAS_ID_5185,GWAS_ID_5186,GWAS_ID_5187,GWAS_ID_5188,GWAS_ID_5189,GWAS_ID_5190,GWAS_ID_5191,GWAS_ID_5192,GWAS_ID_5193,GWAS_ID_5194,GWAS_ID_5195,GWAS_ID_5196,GWAS_ID_5197,GWAS_ID_5198,GWAS_ID_5199,GWAS_ID_5200,GWAS_ID_5201,GWAS_ID_5202,GWAS_ID_5203,GWAS_ID_5204,GWAS_ID_5205,GWAS_ID_5206,GWAS_ID_5207,GWAS_ID_5208,GWAS_ID_5209,GWAS_ID_5210,GWAS_ID_5211,GWAS_ID_5212,GWAS_ID_5213,GWAS_ID_5214,GWAS_ID_5215,GWAS_ID_5216,GWAS_ID_5217,GWAS_ID_5218,GWAS_ID_5219,GWAS_ID_5220,GWAS_ID_5221,GWAS_ID_5222,GWAS_ID_5223,GWAS_ID_5224,GWAS_ID_5225,GWAS_ID_5226,GWAS_ID_5227,GWAS_ID_5228,GWAS_ID_5229,GWAS_ID_5230,GWAS_ID_5231,GWAS_ID_5232,GWAS_ID_5233,GWAS_ID_5234,GWAS_ID_5235,GWAS_ID_5236,GWAS_ID_5237,GWAS_ID_5238,GWAS_ID_5239,GWAS_ID_5240,GWAS_ID_5241,GWAS_ID_5242,GWAS_ID_5243,GWAS_ID_5244,GWAS_ID_5245,GWAS_ID_5246,GWAS_ID_5247,GWAS_ID_5248,GWAS_ID_5249,GWAS_ID_5250,GWAS_ID_5251,GWAS_ID_5252,GWAS_ID_5253,GWAS_ID_5254,GWAS_ID_5255,GWAS_ID_5256 RMVar_hsa_circ_23393,RMVar_hsa_circ_3562,RMVar_hsa_circ_144816,RMVar_hsa_circ_81412,RMVar_hsa_circ_355111,RMVar_hsa_circ_60465,RMVar_hsa_circ_360231,RMVar_hsa_circ_309707,RMVar_hsa_circ_44813,RMVar_hsa_circ_144817,RMVar_hsa_circ_144818,RMVar_hsa_circ_35626,RMVar_hsa_circ_343648,RMVar_hsa_circ_347467,RMVar_hsa_circ_317366,RMVar_hsa_circ_98388,RMVar_hsa_circ_144820,RMVar_hsa_circ_144819,RMVar_hsa_circ_282796,RMVar_hsa_circ_342668,RMVar_hsa_circ_144822,RMVar_hsa_circ_144823 45197 RMVar_ID_45197 Human_SNP_ID_441681397 A-to-I Human chr10 + 89724782 89724782 89724782 GGGATTACAGGCACACACCACCACGCCCAGCTAATTTTTGTGTTTTTAGTAGAGACGGTGTTGCT GGGATTACAGGCACACACCACCACGCCCAGCTGATTTTTGTGTTTTTAGTAGAGACGGTGTTGCT A G KIF20B Ensembl:ENSG00000138182 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs555881456 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23393,RMVar_hsa_circ_3562,RMVar_hsa_circ_144816,RMVar_hsa_circ_81412,RMVar_hsa_circ_355111,RMVar_hsa_circ_60465,RMVar_hsa_circ_309707,RMVar_hsa_circ_44813,RMVar_hsa_circ_144817,RMVar_hsa_circ_144818,RMVar_hsa_circ_35626,RMVar_hsa_circ_343648,RMVar_hsa_circ_347467,RMVar_hsa_circ_317366,RMVar_hsa_circ_98388,RMVar_hsa_circ_144820,RMVar_hsa_circ_144819,RMVar_hsa_circ_282796,RMVar_hsa_circ_342668,RMVar_hsa_circ_144822,RMVar_hsa_circ_144823,RMVar_hsa_circ_9399,RMVar_hsa_circ_368250 45198 RMVar_ID_45198 Human_SNP_ID_74395299 A-to-I Human chr2 - 60735361 60735361 60735361 TTTCTAAAACCATATACTTTAGAAGAACAGAAAAACCTCACAGTCTGTCCTGATGGAGCACTTTT TTTCTAAAACCATATACTTTAGAAGAACAGAAGAACCTCACAGTCTGTCCTGATGGAGCACTTTT T C ATP1B3P1 Ensembl:ENSG00000271707 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879188828 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5590686,Human_RBP_ID_8258007,Human_RBP_ID_18533676 Human_miRNA_ID_1823096,Human_miRNA_ID_1874344,Human_miRNA_ID_1878007,Human_miRNA_ID_1883580 45199 RMVar_ID_45199 Human_SNP_ID_74407442 A-to-I Human chr2 + 60778981 60778981 60778981 ATGGTGGTGCACCCCTGTAATCATAGCTACGCAAGAGGCTGAGGTGGAGGATCAGTTGAGCCCAG ATGGTGGTGCACCCCTGTAATCATAGCTACGCGAGAGGCTGAGGTGGAGGATCAGTTGAGCCCAG A G PAPOLG Ensembl:ENSG00000115421 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs78555650 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6934511 RMVar_hsa_circ_1177,RMVar_hsa_circ_14081,RMVar_hsa_circ_343081,RMVar_hsa_circ_27599,RMVar_hsa_circ_18764,RMVar_hsa_circ_32109,RMVar_hsa_circ_9722,RMVar_hsa_circ_10342,RMVar_hsa_circ_106326,RMVar_hsa_circ_316938,RMVar_hsa_circ_200187,RMVar_hsa_circ_330999,RMVar_hsa_circ_326244,RMVar_hsa_circ_41235,RMVar_hsa_circ_57949,RMVar_hsa_circ_200188 45200 RMVar_ID_45200 Human_SNP_ID_74410351 A-to-I Human chr2 + 60789473 60789473 60789473 CCCAGGCTGATCTCGAACTCCTGGGCTCAAGCAATTTGCCCACCTTGGCCTCTTTAAAGTGCTGG CCCAGGCTGATCTCGAACTCCTGGGCTCAAGCGATTTGCCCACCTTGGCCTCTTTAAAGTGCTGG A G PAPOLG Ensembl:ENSG00000115421 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1260031483 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1177,RMVar_hsa_circ_18764,RMVar_hsa_circ_32109,RMVar_hsa_circ_9722,RMVar_hsa_circ_106326,RMVar_hsa_circ_200187,RMVar_hsa_circ_91733,RMVar_hsa_circ_62717,RMVar_hsa_circ_41235,RMVar_hsa_circ_38777,RMVar_hsa_circ_200195,RMVar_hsa_circ_288607,RMVar_hsa_circ_300948,RMVar_hsa_circ_73763,RMVar_hsa_circ_200197,RMVar_hsa_circ_200198 45201 RMVar_ID_45201 Human_SNP_ID_74440492 A-to-I Human chr2 + 60903736 60903736 60903736 TATTTTTATTAGACACAGGGTTTCACCATGTCAGCCAGCCTGGTGTTGAACTCCCAACCTCAAGT TATTTTTATTAGACACAGGGTTTCACCATGTCGGCCAGCCTGGTGTTGAACTCCCAACCTCAAGT A G REL Ensembl:ENSG00000162924 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1313434215 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_200201,RMVar_hsa_circ_265062,RMVar_hsa_circ_66548,RMVar_hsa_circ_72942,RMVar_hsa_circ_79042,RMVar_hsa_circ_98550,RMVar_hsa_circ_200200,RMVar_hsa_circ_352784,RMVar_hsa_circ_200204,RMVar_hsa_circ_348953,RMVar_hsa_circ_200205 45202 RMVar_ID_45202 Human_SNP_ID_74441607 A-to-I Human chr2 + 60907369 60907369 60907369 AAGAAGCTTAATTAAAATGTGTTAAAAGGGCCAGGCACGGTGGCTCATGCCTGTAATCCCAGCCC AAGAAGCTTAATTAAAATGTGTTAAAAGGGCCGGGCACGGTGGCTCATGCCTGTAATCCCAGCCC A G REL Ensembl:ENSG00000162924 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs988755721 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_200201,RMVar_hsa_circ_265062,RMVar_hsa_circ_66548,RMVar_hsa_circ_72942,RMVar_hsa_circ_79042,RMVar_hsa_circ_98550,RMVar_hsa_circ_200200,RMVar_hsa_circ_352784,RMVar_hsa_circ_200204,RMVar_hsa_circ_348953,RMVar_hsa_circ_200205 45203 RMVar_ID_45203 Human_SNP_ID_74441633 A-to-I Human chr2 + 60907473 60907473 60907473 CGAGACCAGCCTGGGCAATGTGGTGAAACCCCATCTCTACAAAAAATTGGCTGGGCATGGGTGCG CGAGACCAGCCTGGGCAATGTGGTGAAACCCCGTCTCTACAAAAAATTGGCTGGGCATGGGTGCG A G REL Ensembl:ENSG00000162924 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs559969158 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22595390 RMVar_hsa_circ_200201,RMVar_hsa_circ_265062,RMVar_hsa_circ_66548,RMVar_hsa_circ_72942,RMVar_hsa_circ_79042,RMVar_hsa_circ_98550,RMVar_hsa_circ_200200,RMVar_hsa_circ_352784,RMVar_hsa_circ_200204,RMVar_hsa_circ_348953,RMVar_hsa_circ_200205 45204 RMVar_ID_45204 Human_SNP_ID_74447897 A-to-I Human chr2 - 60932215 60932215 60932215 GGAGGCCAAGGCGGGTGAATCACTTGAGCCCAAGAGTTTGAGACCAGCCTGGGTAACATGATGAA GGAGGCCAAGGCGGGTGAATCACTTGAGCCCAGGAGTTTGAGACCAGCCTGGGTAACATGATGAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1185305577 Functional Loss SNV dbSNP153 33..33 33 - - - 45205 RMVar_ID_45205 Human_SNP_ID_74448269 A-to-I Human chr2 + 60933800 60933800 60933800 TTTTATGCCAGTACAAAAATGTTTTGATTACTATGGCTTTGTAGTAATTTTGAAATCAGGTATTG TTTTATGCCAGTACAAAAATGTTTTGATTACTGTGGCTTTGTAGTAATTTTGAAATCAGGTATTG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569198112 Functional Loss SNV dbSNP153 33..33 33 - - - 45206 RMVar_ID_45206 Human_SNP_ID_74470615 A-to-I Human chr2 + 61022756 61022756 61022756 AGGTGTAGTGGTGTGTGCCTGTAGTCCTAGCCACTAGGGAGGCTGAGGTGGGAGGATCCCTTTGA AGGTGTAGTGGTGTGTGCCTGTAGTCCTAGCCTCTAGGGAGGCTGAGGTGGGAGGATCCCTTTGA A T PEX13 Ensembl:ENSG00000162928 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1230086109 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13925727,Human_RBP_ID_25553415 RMVar_hsa_circ_200215,RMVar_hsa_circ_108845 45207 RMVar_ID_45207 Human_SNP_ID_74470941 A-to-I Human chr2 + 61023859 61023859 61023859 CACTCTGTCACCAGGCTGGAGTGTGGTGACGCAATCACACCTCACTGCAGCTTCCATCTCCCAGG CACTCTGTCACCAGGCTGGAGTGTGGTGACGCCATCACACCTCACTGCAGCTTCCATCTCCCAGG A C PEX13 Ensembl:ENSG00000162928 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1255469166 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_200215,RMVar_hsa_circ_108845 45208 RMVar_ID_45208 Human_SNP_ID_74470948 A-to-I Human chr2 + 61023875 61023875 61023875 TGGAGTGTGGTGACGCAATCACACCTCACTGCAGCTTCCATCTCCCAGGGCTCAAGCAGTCCTCC TGGAGTGTGGTGACGCAATCACACCTCACTGCGGCTTCCATCTCCCAGGGCTCAAGCAGTCCTCC A G PEX13 Ensembl:ENSG00000162928 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs889488057 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_200215,RMVar_hsa_circ_108845 45209 RMVar_ID_45209 Human_SNP_ID_74472383 A-to-I Human chr2 + 61028615 61028615 61028615 CACCATGTTGGCCAGGCTGGTCTCGAACTCCTAACCTGAGGGGACCCGCCTGCCTCAGCCTCCCA CACCATGTTGGCCAGGCTGGTCTCGAACTCCTTACCTGAGGGGACCCGCCTGCCTCAGCCTCCCA A T PEX13 Ensembl:ENSG00000162928 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355234069 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_200215,RMVar_hsa_circ_108845 45210 RMVar_ID_45210 Human_SNP_ID_74475893 A-to-I Human chr2 + 61041206 61041206 61041206 CAAAAAGTATCCGGGTGTGGTGGTGCATGCCTATAGTCCCAGTTACTTGGGAGGCTGAGATGGGA CAAAAAGTATCCGGGTGTGGTGGTGCATGCCTCTAGTCCCAGTTACTTGGGAGGCTGAGATGGGA A C PEX13 Ensembl:ENSG00000162928 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1488185585 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_200217,RMVar_hsa_circ_376111,RMVar_hsa_circ_200218 45211 RMVar_ID_45211 Human_SNP_ID_74475894 A-to-I Human chr2 + 61041206 61041206 61041206 CAAAAAGTATCCGGGTGTGGTGGTGCATGCCTATAGTCCCAGTTACTTGGGAGGCTGAGATGGGA CAAAAAGTATCCGGGTGTGGTGGTGCATGCCTGTAGTCCCAGTTACTTGGGAGGCTGAGATGGGA A G PEX13 Ensembl:ENSG00000162928 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1488185585 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_200217,RMVar_hsa_circ_376111,RMVar_hsa_circ_200218 45212 RMVar_ID_45212 Human_SNP_ID_74478071 A-to-I Human chr2 + 61049652 61049652 61049652 AAAATTAGCTAGGTGTGGTGGCACATGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTAGCTAGGTGTGGTGGCACATGCCTGTGATCCCAGCTACTCGGGAGGCTGAGGCAGGAGA A G PEX13 Ensembl:ENSG00000162928 Protein coding 3'UTR GSE38233;GSE100210;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,29129909,31158229,31158229,31158229,31158229,31158229,31158229,32596459,32596459 RNA-Seq:(High) rs960725016 Functional Loss SNV dbSNP153 33..33 33 - - - 45213 RMVar_ID_45213 Human_SNP_ID_74478073 A-to-I Human chr2 + 61049658 61049658 61049658 AGCTAGGTGTGGTGGCACATGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCT AGCTAGGTGTGGTGGCACATGCCTGTAATCCCTGCTACTCGGGAGGCTGAGGCAGGAGAATTGCT A T PEX13 Ensembl:ENSG00000162928 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1009506628 Functional Loss SNV dbSNP153 33..33 33 - - - 45214 RMVar_ID_45214 Human_SNP_ID_74478078 A-to-I Human chr2 + 61049679 61049679 61049679 CCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCTTGAACCCCAGGAGGCGGAGGT CCTGTAATCCCAGCTACTCGGGAGGCTGAGGCGGGAGAATTGCTTGAACCCCAGGAGGCGGAGGT A G PEX13 Ensembl:ENSG00000162928 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,31158229,32596459 RNA-Seq:(High) rs540470939 Functional Loss SNV dbSNP153 33..33 33 - - - 45215 RMVar_ID_45215 Human_SNP_ID_74478218 A-to-I Human chr2 + 61050269 61050269 61050269 GCAGTGGCGTGCACCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCCG GCAGTGGCGTGCACCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCCG A G PEX13 Ensembl:ENSG00000162928 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1559048419 Functional Loss SNV dbSNP153 33..33 33 - - - 45216 RMVar_ID_45216 Human_SNP_ID_74478227 A-to-I Human chr2 + 61050308 61050308 61050308 TGAGGCAGGAGAATCACTTGAACCCGGGAGGCAGAGGTTGCAGGGAGCTGAGATCATGCCACTGC TGAGGCAGGAGAATCACTTGAACCCGGGAGGCGGAGGTTGCAGGGAGCTGAGATCATGCCACTGC A G PEX13 Ensembl:ENSG00000162928 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1353263772 Functional Loss SNV dbSNP153 33..33 33 - - - 45217 RMVar_ID_45217 Human_SNP_ID_74478242 A-to-I Human chr2 + 61050351 61050351 61050351 GGAGCTGAGATCATGCCACTGCACTCCAGCCTAGGGGACAGAGCAAGACTCTGTCTCAAAACAAA GGAGCTGAGATCATGCCACTGCACTCCAGCCTGGGGGACAGAGCAAGACTCTGTCTCAAAACAAA A G PEX13 Ensembl:ENSG00000162928 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1200105237 Functional Loss SNV dbSNP153 33..33 33 - - - 45218 RMVar_ID_45218 Human_SNP_ID_74478316 A-to-I Human chr2 + 61050651 61050651 61050651 TTTTCTTTTGTCTTTTTTTGAAACGGAGTCTCACTCTGTCGCCCAGGCTGGAGTCCAGTGGCGCG TTTTCTTTTGTCTTTTTTTGAAACGGAGTCTCTCTCTGTCGCCCAGGCTGGAGTCCAGTGGCGCG A T PEX13 Ensembl:ENSG00000162928 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560282307 Functional Loss SNV dbSNP153 33..33 33 - - - 45219 RMVar_ID_45219 Human_SNP_ID_74488936 A-to-I Human chr2 + 61088551 61088551 61088551 AGTTGTTGTTGTTGTTTTGGAGACGGAGTCTTACTCTGTCACCCAGGCTGGCGTGCAGTGGTGTG AGTTGTTGTTGTTGTTTTGGAGACGGAGTCTTTCTCTGTCACCCAGGCTGGCGTGCAGTGGTGTG A T KIAA1841 Ensembl:ENSG00000162929 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1194303780 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82780,RMVar_hsa_circ_373148,RMVar_hsa_circ_361179,RMVar_hsa_circ_89136,RMVar_hsa_circ_200221,RMVar_hsa_circ_43283,RMVar_hsa_circ_200222,RMVar_hsa_circ_200220,RMVar_hsa_circ_269068,RMVar_hsa_circ_200229,RMVar_hsa_circ_49002,RMVar_hsa_circ_297108,RMVar_hsa_circ_336290,RMVar_hsa_circ_20953,RMVar_hsa_circ_289432,RMVar_hsa_circ_200227,RMVar_hsa_circ_370100,RMVar_hsa_circ_317519,RMVar_hsa_circ_295773,RMVar_hsa_circ_278191,RMVar_hsa_circ_200231,RMVar_hsa_circ_200232,RMVar_hsa_circ_200230,RMVar_hsa_circ_13061,RMVar_hsa_circ_11935,RMVar_hsa_circ_330698,RMVar_hsa_circ_200228,RMVar_hsa_circ_200238,RMVar_hsa_circ_325825,RMVar_hsa_circ_21068,RMVar_hsa_circ_36356,RMVar_hsa_circ_200240,RMVar_hsa_circ_310911,RMVar_hsa_circ_42345,RMVar_hsa_circ_26046,RMVar_hsa_circ_200242 45220 RMVar_ID_45220 Human_SNP_ID_74489103 A-to-I Human chr2 + 61089282 61089282 61089282 CCTATAATCCCAGCACTTTGGGAGGCCAAGTCAGGTGGATCACCTGAGGTGAGGAGTTTGAGACC CCTATAATCCCAGCACTTTGGGAGGCCAAGTCGGGTGGATCACCTGAGGTGAGGAGTTTGAGACC A G KIAA1841 Ensembl:ENSG00000162929 Protein coding exon GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,31158229,32596459 RNA-Seq:(High) rs1019518149 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82780,RMVar_hsa_circ_373148,RMVar_hsa_circ_361179,RMVar_hsa_circ_89136,RMVar_hsa_circ_200221,RMVar_hsa_circ_43283,RMVar_hsa_circ_200222,RMVar_hsa_circ_200220,RMVar_hsa_circ_269068,RMVar_hsa_circ_200229,RMVar_hsa_circ_49002,RMVar_hsa_circ_297108,RMVar_hsa_circ_336290,RMVar_hsa_circ_20953,RMVar_hsa_circ_289432,RMVar_hsa_circ_200227,RMVar_hsa_circ_370100,RMVar_hsa_circ_317519,RMVar_hsa_circ_295773,RMVar_hsa_circ_278191,RMVar_hsa_circ_200231,RMVar_hsa_circ_200232,RMVar_hsa_circ_200230,RMVar_hsa_circ_13061,RMVar_hsa_circ_11935,RMVar_hsa_circ_330698,RMVar_hsa_circ_200228,RMVar_hsa_circ_200238,RMVar_hsa_circ_325825,RMVar_hsa_circ_21068,RMVar_hsa_circ_36356,RMVar_hsa_circ_200240,RMVar_hsa_circ_310911,RMVar_hsa_circ_42345,RMVar_hsa_circ_26046,RMVar_hsa_circ_200242 45221 RMVar_ID_45221 Human_SNP_ID_74489307 A-to-I Human chr2 + 61090075 61090075 61090075 AGGAGTCTGAGGCAGGAGGATCATTTGATCCCAGGAGTTTGAGGTTGCAGTGAGCTAGGAGCATG AGGAGTCTGAGGCAGGAGGATCATTTGATCCCGGGAGTTTGAGGTTGCAGTGAGCTAGGAGCATG A G KIAA1841 Ensembl:ENSG00000162929 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1468921574 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82780,RMVar_hsa_circ_373148,RMVar_hsa_circ_361179,RMVar_hsa_circ_89136,RMVar_hsa_circ_200221,RMVar_hsa_circ_43283,RMVar_hsa_circ_200222,RMVar_hsa_circ_200220,RMVar_hsa_circ_269068,RMVar_hsa_circ_200229,RMVar_hsa_circ_49002,RMVar_hsa_circ_297108,RMVar_hsa_circ_336290,RMVar_hsa_circ_20953,RMVar_hsa_circ_289432,RMVar_hsa_circ_200227,RMVar_hsa_circ_370100,RMVar_hsa_circ_317519,RMVar_hsa_circ_295773,RMVar_hsa_circ_278191,RMVar_hsa_circ_200231,RMVar_hsa_circ_200232,RMVar_hsa_circ_200230,RMVar_hsa_circ_13061,RMVar_hsa_circ_11935,RMVar_hsa_circ_330698,RMVar_hsa_circ_200228,RMVar_hsa_circ_200238,RMVar_hsa_circ_325825,RMVar_hsa_circ_21068,RMVar_hsa_circ_36356,RMVar_hsa_circ_200240,RMVar_hsa_circ_310911,RMVar_hsa_circ_42345,RMVar_hsa_circ_26046,RMVar_hsa_circ_200242 45222 RMVar_ID_45222 Human_SNP_ID_74489308 A-to-I Human chr2 + 61090075 61090075 61090075 AGGAGTCTGAGGCAGGAGGATCATTTGATCCCAGGAGTTTGAGGTTGCAGTGAGCTAGGAGCATG AGGAGTCTGAGGCAGGAGGATCATTTGATCCCTGGAGTTTGAGGTTGCAGTGAGCTAGGAGCATG A T KIAA1841 Ensembl:ENSG00000162929 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1468921574 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82780,RMVar_hsa_circ_373148,RMVar_hsa_circ_361179,RMVar_hsa_circ_89136,RMVar_hsa_circ_200221,RMVar_hsa_circ_43283,RMVar_hsa_circ_200222,RMVar_hsa_circ_200220,RMVar_hsa_circ_269068,RMVar_hsa_circ_200229,RMVar_hsa_circ_49002,RMVar_hsa_circ_297108,RMVar_hsa_circ_336290,RMVar_hsa_circ_20953,RMVar_hsa_circ_289432,RMVar_hsa_circ_200227,RMVar_hsa_circ_370100,RMVar_hsa_circ_317519,RMVar_hsa_circ_295773,RMVar_hsa_circ_278191,RMVar_hsa_circ_200231,RMVar_hsa_circ_200232,RMVar_hsa_circ_200230,RMVar_hsa_circ_13061,RMVar_hsa_circ_11935,RMVar_hsa_circ_330698,RMVar_hsa_circ_200228,RMVar_hsa_circ_200238,RMVar_hsa_circ_325825,RMVar_hsa_circ_21068,RMVar_hsa_circ_36356,RMVar_hsa_circ_200240,RMVar_hsa_circ_310911,RMVar_hsa_circ_42345,RMVar_hsa_circ_26046,RMVar_hsa_circ_200242 45223 RMVar_ID_45223 Human_SNP_ID_74489447 A-to-I Human chr2 + 61090619 61090619 61090619 AGCTCACTGCAGCCTTGAACTCCTGGACTTTCAAGCAGTCCTCCCACATCAGCCTCCTGAGCTAG AGCTCACTGCAGCCTTGAACTCCTGGACTTTCGAGCAGTCCTCCCACATCAGCCTCCTGAGCTAG A G KIAA1841 Ensembl:ENSG00000162929 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs918649841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_250817 RMVar_hsa_circ_82780,RMVar_hsa_circ_373148,RMVar_hsa_circ_361179,RMVar_hsa_circ_89136,RMVar_hsa_circ_200221,RMVar_hsa_circ_43283,RMVar_hsa_circ_200222,RMVar_hsa_circ_200220,RMVar_hsa_circ_269068,RMVar_hsa_circ_200229,RMVar_hsa_circ_49002,RMVar_hsa_circ_297108,RMVar_hsa_circ_336290,RMVar_hsa_circ_20953,RMVar_hsa_circ_289432,RMVar_hsa_circ_200227,RMVar_hsa_circ_370100,RMVar_hsa_circ_317519,RMVar_hsa_circ_295773,RMVar_hsa_circ_278191,RMVar_hsa_circ_200231,RMVar_hsa_circ_200232,RMVar_hsa_circ_200230,RMVar_hsa_circ_13061,RMVar_hsa_circ_11935,RMVar_hsa_circ_330698,RMVar_hsa_circ_200228,RMVar_hsa_circ_200238,RMVar_hsa_circ_325825,RMVar_hsa_circ_21068,RMVar_hsa_circ_36356,RMVar_hsa_circ_200240,RMVar_hsa_circ_310911,RMVar_hsa_circ_42345,RMVar_hsa_circ_26046,RMVar_hsa_circ_200242 45224 RMVar_ID_45224 Human_SNP_ID_74489453 A-to-I Human chr2 + 61090650 61090650 61090650 CAAGCAGTCCTCCCACATCAGCCTCCTGAGCTAGGACCATGGGTGTGCATCACCATGCCTGGCAA CAAGCAGTCCTCCCACATCAGCCTCCTGAGCTGGGACCATGGGTGTGCATCACCATGCCTGGCAA A G KIAA1841 Ensembl:ENSG00000162929 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs984092746 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23878230 Human_Splice_Rec_250817 RMVar_hsa_circ_82780,RMVar_hsa_circ_373148,RMVar_hsa_circ_361179,RMVar_hsa_circ_89136,RMVar_hsa_circ_200221,RMVar_hsa_circ_43283,RMVar_hsa_circ_200222,RMVar_hsa_circ_200220,RMVar_hsa_circ_269068,RMVar_hsa_circ_200229,RMVar_hsa_circ_49002,RMVar_hsa_circ_297108,RMVar_hsa_circ_336290,RMVar_hsa_circ_20953,RMVar_hsa_circ_289432,RMVar_hsa_circ_200227,RMVar_hsa_circ_370100,RMVar_hsa_circ_317519,RMVar_hsa_circ_295773,RMVar_hsa_circ_278191,RMVar_hsa_circ_200231,RMVar_hsa_circ_200232,RMVar_hsa_circ_200230,RMVar_hsa_circ_13061,RMVar_hsa_circ_11935,RMVar_hsa_circ_330698,RMVar_hsa_circ_200228,RMVar_hsa_circ_200238,RMVar_hsa_circ_325825,RMVar_hsa_circ_21068,RMVar_hsa_circ_36356,RMVar_hsa_circ_200240,RMVar_hsa_circ_310911,RMVar_hsa_circ_42345,RMVar_hsa_circ_26046,RMVar_hsa_circ_200242 45225 RMVar_ID_45225 Human_SNP_ID_74489617 A-to-I Human chr2 + 61091012 61091012 61091012 ATCACTGCAGCCTCCACCTCCCAGGTTCAAGCAGTTCTTCTGCCTCAGACTCAGCCTCCCGAGTA ATCACTGCAGCCTCCACCTCCCAGGTTCAAGCGGTTCTTCTGCCTCAGACTCAGCCTCCCGAGTA A G KIAA1841 Ensembl:ENSG00000162929 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs937317414 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82780,RMVar_hsa_circ_373148,RMVar_hsa_circ_361179,RMVar_hsa_circ_89136,RMVar_hsa_circ_200221,RMVar_hsa_circ_43283,RMVar_hsa_circ_200222,RMVar_hsa_circ_200220,RMVar_hsa_circ_269068,RMVar_hsa_circ_200229,RMVar_hsa_circ_49002,RMVar_hsa_circ_297108,RMVar_hsa_circ_336290,RMVar_hsa_circ_20953,RMVar_hsa_circ_289432,RMVar_hsa_circ_200227,RMVar_hsa_circ_370100,RMVar_hsa_circ_317519,RMVar_hsa_circ_295773,RMVar_hsa_circ_278191,RMVar_hsa_circ_200231,RMVar_hsa_circ_200232,RMVar_hsa_circ_200230,RMVar_hsa_circ_13061,RMVar_hsa_circ_11935,RMVar_hsa_circ_330698,RMVar_hsa_circ_200228,RMVar_hsa_circ_200238,RMVar_hsa_circ_325825,RMVar_hsa_circ_21068,RMVar_hsa_circ_36356,RMVar_hsa_circ_200240,RMVar_hsa_circ_310911,RMVar_hsa_circ_42345,RMVar_hsa_circ_26046,RMVar_hsa_circ_200242 45226 RMVar_ID_45226 Human_SNP_ID_74491229 A-to-I Human chr2 + 61097047 61097047 61097047 GTGGTTGTGCGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAATCTG GTGGTTGTGCGCGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCTTGAATCTG A G KIAA1841 Ensembl:ENSG00000162929 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1462876171 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2011,RMVar_hsa_circ_82780,RMVar_hsa_circ_373148,RMVar_hsa_circ_89136,RMVar_hsa_circ_200221,RMVar_hsa_circ_43283,RMVar_hsa_circ_200222,RMVar_hsa_circ_200220,RMVar_hsa_circ_269068,RMVar_hsa_circ_200229,RMVar_hsa_circ_49002,RMVar_hsa_circ_336290,RMVar_hsa_circ_20953,RMVar_hsa_circ_370100,RMVar_hsa_circ_317519,RMVar_hsa_circ_295773,RMVar_hsa_circ_278191,RMVar_hsa_circ_200231,RMVar_hsa_circ_200230,RMVar_hsa_circ_13061,RMVar_hsa_circ_11935,RMVar_hsa_circ_330698,RMVar_hsa_circ_200228,RMVar_hsa_circ_200238,RMVar_hsa_circ_325825,RMVar_hsa_circ_21068,RMVar_hsa_circ_36356,RMVar_hsa_circ_200240,RMVar_hsa_circ_310911,RMVar_hsa_circ_26046,RMVar_hsa_circ_200242,RMVar_hsa_circ_29283,RMVar_hsa_circ_294470,RMVar_hsa_circ_305395,RMVar_hsa_circ_51216,RMVar_hsa_circ_3107,RMVar_hsa_circ_200243,RMVar_hsa_circ_200244 45227 RMVar_ID_45227 Human_SNP_ID_74496071 A-to-I Human chr2 + 61114635 61114635 61114635 GGACTTGCATATATATATGTGTGTATCTATGTATATATACATGCATGTGTATATACACATACATA GGACTTGCATATATATATGTGTGTATCTATGTGTATATACATGCATGTGTATATACACATACATA A G KIAA1841 Ensembl:ENSG00000162929 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223486017 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82780,RMVar_hsa_circ_373148,RMVar_hsa_circ_200221,RMVar_hsa_circ_200220,RMVar_hsa_circ_269068,RMVar_hsa_circ_49002,RMVar_hsa_circ_317519,RMVar_hsa_circ_29283,RMVar_hsa_circ_305395,RMVar_hsa_circ_51216,RMVar_hsa_circ_19245,RMVar_hsa_circ_200246,RMVar_hsa_circ_200245,RMVar_hsa_circ_200244,RMVar_hsa_circ_288440,RMVar_hsa_circ_327305,RMVar_hsa_circ_277772,RMVar_hsa_circ_200248,RMVar_hsa_circ_200247,RMVar_hsa_circ_32612,RMVar_hsa_circ_307529,RMVar_hsa_circ_344932,RMVar_hsa_circ_355320,RMVar_hsa_circ_118836,RMVar_hsa_circ_200251,RMVar_hsa_circ_200252,RMVar_hsa_circ_308853,RMVar_hsa_circ_127122,RMVar_hsa_circ_30899,RMVar_hsa_circ_200254,RMVar_hsa_circ_62739,RMVar_hsa_circ_200255,RMVar_hsa_circ_200256,RMVar_hsa_circ_90793,RMVar_hsa_circ_200257,RMVar_hsa_circ_200258 45228 RMVar_ID_45228 Human_SNP_ID_74496095 A-to-I Human chr2 + 61114724 61114724 61114724 TTGCCCAGGCTTCAATGCCGTGTCGTGATCACAGCTCACTGCAGCCTCGACCTCCCAAGGCTCAA TTGCCCAGGCTTCAATGCCGTGTCGTGATCACGGCTCACTGCAGCCTCGACCTCCCAAGGCTCAA A G KIAA1841 Ensembl:ENSG00000162929 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1460426208 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24376437 RMVar_hsa_circ_82780,RMVar_hsa_circ_373148,RMVar_hsa_circ_200221,RMVar_hsa_circ_200220,RMVar_hsa_circ_269068,RMVar_hsa_circ_49002,RMVar_hsa_circ_317519,RMVar_hsa_circ_29283,RMVar_hsa_circ_305395,RMVar_hsa_circ_51216,RMVar_hsa_circ_19245,RMVar_hsa_circ_200246,RMVar_hsa_circ_200245,RMVar_hsa_circ_200244,RMVar_hsa_circ_288440,RMVar_hsa_circ_327305,RMVar_hsa_circ_277772,RMVar_hsa_circ_200248,RMVar_hsa_circ_200247,RMVar_hsa_circ_32612,RMVar_hsa_circ_307529,RMVar_hsa_circ_344932,RMVar_hsa_circ_355320,RMVar_hsa_circ_118836,RMVar_hsa_circ_200251,RMVar_hsa_circ_200252,RMVar_hsa_circ_308853,RMVar_hsa_circ_127122,RMVar_hsa_circ_30899,RMVar_hsa_circ_200254,RMVar_hsa_circ_62739,RMVar_hsa_circ_200255,RMVar_hsa_circ_200256,RMVar_hsa_circ_90793,RMVar_hsa_circ_200257,RMVar_hsa_circ_200258 45229 RMVar_ID_45229 Human_SNP_ID_74497492 A-to-I Human chr2 + 61119894 61119894 61119894 TGAAGTAGGAGGATCGCTTGAGCCTGGGAGGCAGAAGTTGCAATGAGCCAAGAGCACGCCACTAC TGAAGTAGGAGGATCGCTTGAGCCTGGGAGGCGGAAGTTGCAATGAGCCAAGAGCACGCCACTAC A G KIAA1841,AC016747.4 Ensembl:ENSG00000162929,Ensembl:ENSG00000274769 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1449414179 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82780,RMVar_hsa_circ_200220,RMVar_hsa_circ_269068,RMVar_hsa_circ_29283,RMVar_hsa_circ_41771,RMVar_hsa_circ_19245,RMVar_hsa_circ_200246,RMVar_hsa_circ_32612,RMVar_hsa_circ_355320,RMVar_hsa_circ_118836,RMVar_hsa_circ_200252,RMVar_hsa_circ_62739,RMVar_hsa_circ_200255,RMVar_hsa_circ_200263,RMVar_hsa_circ_342461,RMVar_hsa_circ_200259,RMVar_hsa_circ_308656,RMVar_hsa_circ_200264 45230 RMVar_ID_45230 Human_SNP_ID_74497493 A-to-I Human chr2 + 61119896 61119896 61119896 AAGTAGGAGGATCGCTTGAGCCTGGGAGGCAGAAGTTGCAATGAGCCAAGAGCACGCCACTACAC AAGTAGGAGGATCGCTTGAGCCTGGGAGGCAGGAGTTGCAATGAGCCAAGAGCACGCCACTACAC A G KIAA1841,AC016747.4 Ensembl:ENSG00000162929,Ensembl:ENSG00000274769 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1377213080 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82780,RMVar_hsa_circ_200220,RMVar_hsa_circ_269068,RMVar_hsa_circ_29283,RMVar_hsa_circ_41771,RMVar_hsa_circ_19245,RMVar_hsa_circ_200246,RMVar_hsa_circ_32612,RMVar_hsa_circ_355320,RMVar_hsa_circ_118836,RMVar_hsa_circ_200252,RMVar_hsa_circ_62739,RMVar_hsa_circ_200255,RMVar_hsa_circ_200263,RMVar_hsa_circ_342461,RMVar_hsa_circ_200259,RMVar_hsa_circ_308656,RMVar_hsa_circ_200264 45231 RMVar_ID_45231 Human_SNP_ID_74497579 A-to-I Human chr2 + 61120241 61120241 61120241 AAAAGAACATTGGACCGGGTGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGC AAAAGAACATTGGACCGGGTGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGC A G KIAA1841,AC016747.4 Ensembl:ENSG00000162929,Ensembl:ENSG00000274769 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs990427690 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82780,RMVar_hsa_circ_200220,RMVar_hsa_circ_269068,RMVar_hsa_circ_29283,RMVar_hsa_circ_41771,RMVar_hsa_circ_19245,RMVar_hsa_circ_200246,RMVar_hsa_circ_32612,RMVar_hsa_circ_355320,RMVar_hsa_circ_118836,RMVar_hsa_circ_200252,RMVar_hsa_circ_62739,RMVar_hsa_circ_200255,RMVar_hsa_circ_200263,RMVar_hsa_circ_342461,RMVar_hsa_circ_200259,RMVar_hsa_circ_308656,RMVar_hsa_circ_200264 45232 RMVar_ID_45232 Human_SNP_ID_74497643 A-to-I Human chr2 + 61120393 61120393 61120393 GTGGTGGTGCAGGCCTGTAATCCCATCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCCG GTGGTGGTGCAGGCCTGTAATCCCATCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCCG A G KIAA1841,AC016747.4 Ensembl:ENSG00000162929,Ensembl:ENSG00000274769 Protein coding,lincRNA intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1262391457 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82780,RMVar_hsa_circ_200220,RMVar_hsa_circ_269068,RMVar_hsa_circ_29283,RMVar_hsa_circ_41771,RMVar_hsa_circ_19245,RMVar_hsa_circ_200246,RMVar_hsa_circ_32612,RMVar_hsa_circ_355320,RMVar_hsa_circ_118836,RMVar_hsa_circ_200252,RMVar_hsa_circ_62739,RMVar_hsa_circ_200255,RMVar_hsa_circ_200263,RMVar_hsa_circ_342461,RMVar_hsa_circ_200259,RMVar_hsa_circ_308656,RMVar_hsa_circ_200264 45233 RMVar_ID_45233 Human_SNP_ID_74497648 A-to-I Human chr2 + 61120406 61120406 61120406 CCTGTAATCCCATCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCCGGAAGGTTGAGGTT CCTGTAATCCCATCTACTCAGGAGGCTGAGGCGGGAGAATCACTTGAACCCGGAAGGTTGAGGTT A G KIAA1841,AC016747.4 Ensembl:ENSG00000162929,Ensembl:ENSG00000274769 Protein coding,lincRNA intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1017877927 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82780,RMVar_hsa_circ_200220,RMVar_hsa_circ_269068,RMVar_hsa_circ_29283,RMVar_hsa_circ_41771,RMVar_hsa_circ_19245,RMVar_hsa_circ_200246,RMVar_hsa_circ_32612,RMVar_hsa_circ_355320,RMVar_hsa_circ_118836,RMVar_hsa_circ_200252,RMVar_hsa_circ_62739,RMVar_hsa_circ_200255,RMVar_hsa_circ_200263,RMVar_hsa_circ_342461,RMVar_hsa_circ_200259,RMVar_hsa_circ_308656,RMVar_hsa_circ_200264 45234 RMVar_ID_45234 Human_SNP_ID_74497653 A-to-I Human chr2 + 61120415 61120415 61120415 CCATCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCCGGAAGGTTGAGGTTGCAGTGAGC CCATCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGGAAGGTTGAGGTTGCAGTGAGC A G KIAA1841,AC016747.4 Ensembl:ENSG00000162929,Ensembl:ENSG00000274769 Protein coding,lincRNA intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs997667475 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82780,RMVar_hsa_circ_200220,RMVar_hsa_circ_269068,RMVar_hsa_circ_29283,RMVar_hsa_circ_41771,RMVar_hsa_circ_19245,RMVar_hsa_circ_200246,RMVar_hsa_circ_32612,RMVar_hsa_circ_355320,RMVar_hsa_circ_118836,RMVar_hsa_circ_200252,RMVar_hsa_circ_62739,RMVar_hsa_circ_200255,RMVar_hsa_circ_200263,RMVar_hsa_circ_342461,RMVar_hsa_circ_200259,RMVar_hsa_circ_308656,RMVar_hsa_circ_200264 45235 RMVar_ID_45235 Human_SNP_ID_74502732 A-to-I Human chr2 - 61140279 61140277 61140279 GTCCTTGCTCTGTTTTTTTTTTTTTTTTTTTGAGGGTCTTGTTCTGTCACCCAGGTTGAGTGGCA GTCCTTGCTCTGTTTTTTTTTTTTTTTTTTTG__GGTCTTGTTCTGTCACCCAGGTTGAGTGGCA CCT C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1212966316 Functional Loss DEL dbSNP153 33..34 33 - - - 45236 RMVar_ID_45236 Human_SNP_ID_74502733 A-to-I Human chr2 - 61140279 61140278 61140279 GTCCTTGCTCTGTTTTTTTTTTTTTTTTTTTGAGGGTCTTGTTCTGTCACCCAGGTTGAGTGGCA GTCCTTGCTCTGTTTTTTTTTTTTTTTTTTTG_GGGTCTTGTTCTGTCACCCAGGTTGAGTGGCA CT C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348549459 Functional Loss DEL dbSNP153 33..33 33 - - - 45237 RMVar_ID_45237 Human_SNP_ID_74502868 A-to-I Human chr2 - 61140750 61140750 61140750 GCAGTCTCACTCTGTCGCCTGGGCTGGAGTGCAGTGGAGCAATCTCAGCTTACTGCAACCTCCGC GCAGTCTCACTCTGTCGCCTGGGCTGGAGTGCGGTGGAGCAATCTCAGCTTACTGCAACCTCCGC T C LOC339803 RNACentral:URS0000D5A0DA lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs995779328 Functional Loss SNV dbSNP153 33..33 33 - - - 45238 RMVar_ID_45238 Human_SNP_ID_74502947 A-to-I Human chr2 - 61141030 61141030 61141030 GTTGCCTAGGCTGGTCTTGAACTCCTGAGTTAAGCTATCTGCCCACCTCGGCCTCCCAAGGTGCT GTTGCCTAGGCTGGTCTTGAACTCCTGAGTTATGCTATCTGCCCACCTCGGCCTCCCAAGGTGCT T A LOC339803,LOC339803:2 RNACentral:URS00008B23CB,RNACentral:URS0000D5A0DA lincRNA,lincRNA exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs570747136 Functional Loss SNV dbSNP153 33..33 33 - - - 45239 RMVar_ID_45239 Human_SNP_ID_74503327 A-to-I Human chr2 - 61142672 61142672 61142672 GTCCCAGCTACTTGGGAAGCTGAGGAAGGAGAATTGCTTGAACCCGGCGGGCAGAGGTTGCAGTA GTCCCAGCTACTTGGGAAGCTGAGGAAGGAGACTTGCTTGAACCCGGCGGGCAGAGGTTGCAGTA T G AC016747.1 Ensembl:ENSG00000212978 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs545821717 Functional Loss SNV dbSNP153 33..33 33 - - - 45240 RMVar_ID_45240 Human_SNP_ID_74503378 A-to-I Human chr2 - 61142856 61142855 61142857 TCAATTAGAAAATGTTTAAATTGGCTGGGCACAGTGTCTCATGCCTCTAATCCCAGCACTTTGGA TCAATTAGAAAATGTTTAAATTGGCTGGGCA__GTGTCTCATGCCTCTAATCCCAGCACTTTGGA CTG C AC016747.1 Ensembl:ENSG00000212978 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs200968648 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_8203332 45241 RMVar_ID_45241 Human_SNP_ID_74504927 A-to-I Human chr2 + 61148165 61148163 61148165 TTATATATAATATATAAAAATGTATATGTATTATATATATAATATATAAAAATATATATGTATAT TTATATATAATATATAAAAATGTATATGTAT__TATATATAATATATAAAAATATATATGTATAT TTA T AC016747.4,C2orf74 Ensembl:ENSG00000274769,Ensembl:ENSG00000237651 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs939059370 Functional Loss DEL dbSNP153 32..33 33 - - - 45242 RMVar_ID_45242 Human_SNP_ID_74505102 A-to-I Human chr2 + 61148778 61148778 61148778 TCGCCTTGTCACCCAGGCTGGAGTGCAATGGCACAATCTCGGCTCACTGCAACCTCCGTCTTCCA TCGCCTTGTCACCCAGGCTGGAGTGCAATGGCCCAATCTCGGCTCACTGCAACCTCCGTCTTCCA A C AC016747.4,C2orf74 Ensembl:ENSG00000274769,Ensembl:ENSG00000237651 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053769054 Functional Loss SNV dbSNP153 33..33 33 - - - 45243 RMVar_ID_45243 Human_SNP_ID_74519568 A-to-I Human chr2 - 61194866 61194866 61194866 TCACCGCAACCTCCGCCTGCCGCGTTCAAGCAATTCTCCTGCGTCAGCCTCCCAAGTAGCTGGGA TCACCGCAACCTCCGCCTGCCGCGTTCAAGCAGTTCTCCTGCGTCAGCCTCCCAAGTAGCTGGGA T C USP34 Ensembl:ENSG00000115464 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1343363488 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4375,RMVar_hsa_circ_102784,RMVar_hsa_circ_121659,RMVar_hsa_circ_200273,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_299364,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_266767,RMVar_hsa_circ_267606,RMVar_hsa_circ_29974,RMVar_hsa_circ_52114,RMVar_hsa_circ_275759,RMVar_hsa_circ_200282,RMVar_hsa_circ_268313,RMVar_hsa_circ_96988,RMVar_hsa_circ_112927,RMVar_hsa_circ_70432,RMVar_hsa_circ_200284,RMVar_hsa_circ_200285,RMVar_hsa_circ_200283 45244 RMVar_ID_45244 Human_SNP_ID_74520608 A-to-I Human chr2 - 61197736 61197736 61197736 AATAGAAGGCGGGCTTGGTGACATGCACATGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGG AATAGAAGGCGGGCTTGGTGACATGCACATGTTGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGG T A USP34 Ensembl:ENSG00000115464 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1328081325 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4375,RMVar_hsa_circ_102784,RMVar_hsa_circ_121659,RMVar_hsa_circ_200273,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_299364,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_266767,RMVar_hsa_circ_267606,RMVar_hsa_circ_29974,RMVar_hsa_circ_52114,RMVar_hsa_circ_275759,RMVar_hsa_circ_200282,RMVar_hsa_circ_268313,RMVar_hsa_circ_96988,RMVar_hsa_circ_112927,RMVar_hsa_circ_70432,RMVar_hsa_circ_200284,RMVar_hsa_circ_200285,RMVar_hsa_circ_200283 45245 RMVar_ID_45245 Human_SNP_ID_74521359 A-to-I Human chr2 - 61200192 61200192 61200192 TTTTAATTAGCCACATGTGGTGTCACACACCTATGGTCCCAGCTACTCAGGAGGCTGAGGTGGAA TTTTAATTAGCCACATGTGGTGTCACACACCTGTGGTCCCAGCTACTCAGGAGGCTGAGGTGGAA T C USP34 Ensembl:ENSG00000115464 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1267054654 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13926348 RMVar_hsa_circ_4375,RMVar_hsa_circ_102784,RMVar_hsa_circ_121659,RMVar_hsa_circ_200273,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_299364,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_266767,RMVar_hsa_circ_267606,RMVar_hsa_circ_29974,RMVar_hsa_circ_52114,RMVar_hsa_circ_275759,RMVar_hsa_circ_200282,RMVar_hsa_circ_268313,RMVar_hsa_circ_96988,RMVar_hsa_circ_112927,RMVar_hsa_circ_70432,RMVar_hsa_circ_200284,RMVar_hsa_circ_200285,RMVar_hsa_circ_200283 45246 RMVar_ID_45246 Human_SNP_ID_74525316 A-to-I Human chr2 - 61214533 61214533 61214533 AGGTCTACAACGTGCTCCTTGGTTTGCTCTCAAGAGCCAAACTTTATGTTGATGCTGCTGTTCAT AGGTCTACAACGTGCTCCTTGGTTTGCTCTCAGGAGCCAAACTTTATGTTGATGCTGCTGTTCAT T C USP34 Ensembl:ENSG00000115464 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs773279213 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9251,Human_RBP_ID_4612698 Human_miRNA_ID_2062176,Human_miRNA_ID_2864652,Human_miRNA_ID_2899846 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_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 45247 RMVar_ID_45247 Human_SNP_ID_74542975 A-to-I Human chr2 - 61269301 61269301 61269301 AAAAAAAAAATTAGCCAAGGTGGTGAGCATCTATAGTCCAAGCTACGCAGGAGGCTGAGCTGGGA AAAAAAAAAATTAGCCAAGGTGGTGAGCATCTGTAGTCCAAGCTACGCAGGAGGCTGAGCTGGGA T C USP34 Ensembl:ENSG00000115464 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1166638126 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_200292,RMVar_hsa_circ_102784,RMVar_hsa_circ_99836,RMVar_hsa_circ_200276,RMVar_hsa_circ_200277,RMVar_hsa_circ_117308,RMVar_hsa_circ_114329,RMVar_hsa_circ_200281,RMVar_hsa_circ_29974,RMVar_hsa_circ_200282,RMVar_hsa_circ_96988,RMVar_hsa_circ_112927,RMVar_hsa_circ_116467,RMVar_hsa_circ_200284,RMVar_hsa_circ_200283,RMVar_hsa_circ_56536,RMVar_hsa_circ_76655,RMVar_hsa_circ_200290,RMVar_hsa_circ_124258,RMVar_hsa_circ_87961,RMVar_hsa_circ_109206,RMVar_hsa_circ_200294,RMVar_hsa_circ_200293,RMVar_hsa_circ_108164,RMVar_hsa_circ_200291,RMVar_hsa_circ_113788,RMVar_hsa_circ_109227,RMVar_hsa_circ_77073,RMVar_hsa_circ_200304,RMVar_hsa_circ_200306,RMVar_hsa_circ_200305,RMVar_hsa_circ_200303,RMVar_hsa_circ_52447,RMVar_hsa_circ_89816,RMVar_hsa_circ_77201,RMVar_hsa_circ_200309,RMVar_hsa_circ_89316,RMVar_hsa_circ_200313,RMVar_hsa_circ_358319,RMVar_hsa_circ_269487,RMVar_hsa_circ_109103,RMVar_hsa_circ_200314,RMVar_hsa_circ_200316,RMVar_hsa_circ_200315,RMVar_hsa_circ_48894,RMVar_hsa_circ_106278,RMVar_hsa_circ_200322,RMVar_hsa_circ_360525,RMVar_hsa_circ_277112,RMVar_hsa_circ_118352,RMVar_hsa_circ_51249,RMVar_hsa_circ_200325,RMVar_hsa_circ_14359,RMVar_hsa_circ_45871,RMVar_hsa_circ_200326,RMVar_hsa_circ_200327,RMVar_hsa_circ_84816,RMVar_hsa_circ_200328,RMVar_hsa_circ_36506,RMVar_hsa_circ_38689,RMVar_hsa_circ_104673,RMVar_hsa_circ_87037,RMVar_hsa_circ_349106,RMVar_hsa_circ_119244,RMVar_hsa_circ_115630,RMVar_hsa_circ_200333,RMVar_hsa_circ_100922,RMVar_hsa_circ_96734,RMVar_hsa_circ_200337,RMVar_hsa_circ_59928,RMVar_hsa_circ_83980,RMVar_hsa_circ_200339,RMVar_hsa_circ_200338,RMVar_hsa_circ_200335,RMVar_hsa_circ_200336,RMVar_hsa_circ_331011,RMVar_hsa_circ_200334,RMVar_hsa_circ_98682,RMVar_hsa_circ_100601,RMVar_hsa_circ_77963,RMVar_hsa_circ_92775,RMVar_hsa_circ_200350,RMVar_hsa_circ_200345,RMVar_hsa_circ_200347,RMVar_hsa_circ_200348,RMVar_hsa_circ_200346,RMVar_hsa_circ_315459,RMVar_hsa_circ_122046,RMVar_hsa_circ_125037,RMVar_hsa_circ_200349,RMVar_hsa_circ_200357,RMVar_hsa_circ_3762,RMVar_hsa_circ_372626,RMVar_hsa_circ_377938,RMVar_hsa_circ_200359,RMVar_hsa_circ_374058,RMVar_hsa_circ_320013,RMVar_hsa_circ_292380,RMVar_hsa_circ_272203,RMVar_hsa_circ_48211,RMVar_hsa_circ_127517,RMVar_hsa_circ_200363,RMVar_hsa_circ_200365,RMVar_hsa_circ_200367,RMVar_hsa_circ_200366,RMVar_hsa_circ_200364,RMVar_hsa_circ_200361,RMVar_hsa_circ_200362,RMVar_hsa_circ_200360,RMVar_hsa_circ_200370,RMVar_hsa_circ_107865,RMVar_hsa_circ_200371,RMVar_hsa_circ_320057,RMVar_hsa_circ_348197,RMVar_hsa_circ_309548,RMVar_hsa_circ_273724,RMVar_hsa_circ_106935,RMVar_hsa_circ_7177,RMVar_hsa_circ_200373,RMVar_hsa_circ_200375,RMVar_hsa_circ_101723,RMVar_hsa_circ_200376,RMVar_hsa_circ_200374,RMVar_hsa_circ_96761,RMVar_hsa_circ_200372,RMVar_hsa_circ_112999,RMVar_hsa_circ_340947,RMVar_hsa_circ_200380,RMVar_hsa_circ_76320,RMVar_hsa_circ_49393,RMVar_hsa_circ_24811,RMVar_hsa_circ_77703,RMVar_hsa_circ_34688,RMVar_hsa_circ_200382,RMVar_hsa_circ_200383,RMVar_hsa_circ_98696,RMVar_hsa_circ_104328,RMVar_hsa_circ_200386,RMVar_hsa_circ_200388,RMVar_hsa_circ_94263,RMVar_hsa_circ_40704,RMVar_hsa_circ_200389,RMVar_hsa_circ_200390,RMVar_hsa_circ_41656,RMVar_hsa_circ_19925,RMVar_hsa_circ_47977,RMVar_hsa_circ_36478,RMVar_hsa_circ_78570,RMVar_hsa_circ_317685,RMVar_hsa_circ_44528,RMVar_hsa_circ_21783,RMVar_hsa_circ_25474,RMVar_hsa_circ_200395,RMVar_hsa_circ_19177,RMVar_hsa_circ_200394,RMVar_hsa_circ_284941,RMVar_hsa_circ_310707,RMVar_hsa_circ_318427,RMVar_hsa_circ_323271,RMVar_hsa_circ_67378,RMVar_hsa_circ_200399,RMVar_hsa_circ_96551,RMVar_hsa_circ_200397,RMVar_hsa_circ_200398,RMVar_hsa_circ_120605,RMVar_hsa_circ_77721,RMVar_hsa_circ_89197,RMVar_hsa_circ_200401,RMVar_hsa_circ_200402,RMVar_hsa_circ_200400 45248 RMVar_ID_45248 Human_SNP_ID_74543016 A-to-I Human chr2 - 61269369 61269366 61269370 TTGAGCCCAGGAGTTGGAGACCAGCCTGGGTAACCTGGTGAAACCCTGTCTCTATTAAAAAAAAA TTGAGCCCAGGAGTTGGAGACCAGCCTGGGT____TGGTGAAACCCTGTCTCTATTAAAAAAAAA AGGTT A USP34 Ensembl:ENSG00000115464 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1400975842 Functional Loss DEL dbSNP153 32..35 33 - - - RMVar_hsa_circ_200292,RMVar_hsa_circ_102784,RMVar_hsa_circ_99836,RMVar_hsa_circ_200276,RMVar_hsa_circ_200277,RMVar_hsa_circ_117308,RMVar_hsa_circ_114329,RMVar_hsa_circ_200281,RMVar_hsa_circ_29974,RMVar_hsa_circ_200282,RMVar_hsa_circ_96988,RMVar_hsa_circ_112927,RMVar_hsa_circ_116467,RMVar_hsa_circ_200284,RMVar_hsa_circ_200283,RMVar_hsa_circ_56536,RMVar_hsa_circ_76655,RMVar_hsa_circ_200290,RMVar_hsa_circ_124258,RMVar_hsa_circ_87961,RMVar_hsa_circ_109206,RMVar_hsa_circ_200294,RMVar_hsa_circ_200293,RMVar_hsa_circ_108164,RMVar_hsa_circ_200291,RMVar_hsa_circ_113788,RMVar_hsa_circ_109227,RMVar_hsa_circ_77073,RMVar_hsa_circ_200304,RMVar_hsa_circ_200306,RMVar_hsa_circ_200305,RMVar_hsa_circ_200303,RMVar_hsa_circ_52447,RMVar_hsa_circ_89816,RMVar_hsa_circ_77201,RMVar_hsa_circ_200309,RMVar_hsa_circ_89316,RMVar_hsa_circ_200313,RMVar_hsa_circ_358319,RMVar_hsa_circ_269487,RMVar_hsa_circ_109103,RMVar_hsa_circ_200314,RMVar_hsa_circ_200316,RMVar_hsa_circ_200315,RMVar_hsa_circ_48894,RMVar_hsa_circ_106278,RMVar_hsa_circ_200322,RMVar_hsa_circ_360525,RMVar_hsa_circ_277112,RMVar_hsa_circ_118352,RMVar_hsa_circ_51249,RMVar_hsa_circ_200325,RMVar_hsa_circ_14359,RMVar_hsa_circ_45871,RMVar_hsa_circ_200326,RMVar_hsa_circ_200327,RMVar_hsa_circ_84816,RMVar_hsa_circ_200328,RMVar_hsa_circ_36506,RMVar_hsa_circ_38689,RMVar_hsa_circ_104673,RMVar_hsa_circ_87037,RMVar_hsa_circ_349106,RMVar_hsa_circ_119244,RMVar_hsa_circ_115630,RMVar_hsa_circ_200333,RMVar_hsa_circ_100922,RMVar_hsa_circ_96734,RMVar_hsa_circ_200337,RMVar_hsa_circ_59928,RMVar_hsa_circ_83980,RMVar_hsa_circ_200339,RMVar_hsa_circ_200338,RMVar_hsa_circ_200335,RMVar_hsa_circ_200336,RMVar_hsa_circ_331011,RMVar_hsa_circ_200334,RMVar_hsa_circ_98682,RMVar_hsa_circ_100601,RMVar_hsa_circ_77963,RMVar_hsa_circ_92775,RMVar_hsa_circ_200350,RMVar_hsa_circ_200345,RMVar_hsa_circ_200347,RMVar_hsa_circ_200348,RMVar_hsa_circ_200346,RMVar_hsa_circ_315459,RMVar_hsa_circ_122046,RMVar_hsa_circ_125037,RMVar_hsa_circ_200349,RMVar_hsa_circ_200357,RMVar_hsa_circ_3762,RMVar_hsa_circ_372626,RMVar_hsa_circ_377938,RMVar_hsa_circ_200359,RMVar_hsa_circ_374058,RMVar_hsa_circ_320013,RMVar_hsa_circ_292380,RMVar_hsa_circ_272203,RMVar_hsa_circ_48211,RMVar_hsa_circ_127517,RMVar_hsa_circ_200363,RMVar_hsa_circ_200365,RMVar_hsa_circ_200367,RMVar_hsa_circ_200366,RMVar_hsa_circ_200364,RMVar_hsa_circ_200361,RMVar_hsa_circ_200362,RMVar_hsa_circ_200360,RMVar_hsa_circ_200370,RMVar_hsa_circ_107865,RMVar_hsa_circ_200371,RMVar_hsa_circ_320057,RMVar_hsa_circ_348197,RMVar_hsa_circ_309548,RMVar_hsa_circ_273724,RMVar_hsa_circ_106935,RMVar_hsa_circ_7177,RMVar_hsa_circ_200373,RMVar_hsa_circ_200375,RMVar_hsa_circ_101723,RMVar_hsa_circ_200376,RMVar_hsa_circ_200374,RMVar_hsa_circ_96761,RMVar_hsa_circ_200372,RMVar_hsa_circ_112999,RMVar_hsa_circ_340947,RMVar_hsa_circ_200380,RMVar_hsa_circ_76320,RMVar_hsa_circ_49393,RMVar_hsa_circ_24811,RMVar_hsa_circ_77703,RMVar_hsa_circ_34688,RMVar_hsa_circ_200382,RMVar_hsa_circ_200383,RMVar_hsa_circ_98696,RMVar_hsa_circ_104328,RMVar_hsa_circ_200386,RMVar_hsa_circ_200388,RMVar_hsa_circ_94263,RMVar_hsa_circ_40704,RMVar_hsa_circ_200389,RMVar_hsa_circ_200390,RMVar_hsa_circ_41656,RMVar_hsa_circ_19925,RMVar_hsa_circ_47977,RMVar_hsa_circ_36478,RMVar_hsa_circ_78570,RMVar_hsa_circ_317685,RMVar_hsa_circ_44528,RMVar_hsa_circ_21783,RMVar_hsa_circ_25474,RMVar_hsa_circ_200395,RMVar_hsa_circ_19177,RMVar_hsa_circ_200394,RMVar_hsa_circ_284941,RMVar_hsa_circ_310707,RMVar_hsa_circ_318427,RMVar_hsa_circ_323271,RMVar_hsa_circ_67378,RMVar_hsa_circ_200399,RMVar_hsa_circ_96551,RMVar_hsa_circ_200397,RMVar_hsa_circ_200398,RMVar_hsa_circ_120605,RMVar_hsa_circ_77721,RMVar_hsa_circ_89197,RMVar_hsa_circ_200401,RMVar_hsa_circ_200402,RMVar_hsa_circ_200400 45249 RMVar_ID_45249 Human_SNP_ID_74543018 A-to-I Human chr2 - 61269369 61269369 61269369 TTGAGCCCAGGAGTTGGAGACCAGCCTGGGTAACCTGGTGAAACCCTGTCTCTATTAAAAAAAAA TTGAGCCCAGGAGTTGGAGACCAGCCTGGGTATCCTGGTGAAACCCTGTCTCTATTAAAAAAAAA T A USP34 Ensembl:ENSG00000115464 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350036780 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_200292,RMVar_hsa_circ_102784,RMVar_hsa_circ_99836,RMVar_hsa_circ_200276,RMVar_hsa_circ_200277,RMVar_hsa_circ_117308,RMVar_hsa_circ_114329,RMVar_hsa_circ_200281,RMVar_hsa_circ_29974,RMVar_hsa_circ_200282,RMVar_hsa_circ_96988,RMVar_hsa_circ_112927,RMVar_hsa_circ_116467,RMVar_hsa_circ_200284,RMVar_hsa_circ_200283,RMVar_hsa_circ_56536,RMVar_hsa_circ_76655,RMVar_hsa_circ_200290,RMVar_hsa_circ_124258,RMVar_hsa_circ_87961,RMVar_hsa_circ_109206,RMVar_hsa_circ_200294,RMVar_hsa_circ_200293,RMVar_hsa_circ_108164,RMVar_hsa_circ_200291,RMVar_hsa_circ_113788,RMVar_hsa_circ_109227,RMVar_hsa_circ_77073,RMVar_hsa_circ_200304,RMVar_hsa_circ_200306,RMVar_hsa_circ_200305,RMVar_hsa_circ_200303,RMVar_hsa_circ_52447,RMVar_hsa_circ_89816,RMVar_hsa_circ_77201,RMVar_hsa_circ_200309,RMVar_hsa_circ_89316,RMVar_hsa_circ_200313,RMVar_hsa_circ_358319,RMVar_hsa_circ_269487,RMVar_hsa_circ_109103,RMVar_hsa_circ_200314,RMVar_hsa_circ_200316,RMVar_hsa_circ_200315,RMVar_hsa_circ_48894,RMVar_hsa_circ_106278,RMVar_hsa_circ_200322,RMVar_hsa_circ_360525,RMVar_hsa_circ_277112,RMVar_hsa_circ_118352,RMVar_hsa_circ_51249,RMVar_hsa_circ_200325,RMVar_hsa_circ_14359,RMVar_hsa_circ_45871,RMVar_hsa_circ_200326,RMVar_hsa_circ_200327,RMVar_hsa_circ_84816,RMVar_hsa_circ_200328,RMVar_hsa_circ_36506,RMVar_hsa_circ_38689,RMVar_hsa_circ_104673,RMVar_hsa_circ_87037,RMVar_hsa_circ_349106,RMVar_hsa_circ_119244,RMVar_hsa_circ_115630,RMVar_hsa_circ_200333,RMVar_hsa_circ_100922,RMVar_hsa_circ_96734,RMVar_hsa_circ_200337,RMVar_hsa_circ_59928,RMVar_hsa_circ_83980,RMVar_hsa_circ_200339,RMVar_hsa_circ_200338,RMVar_hsa_circ_200335,RMVar_hsa_circ_200336,RMVar_hsa_circ_331011,RMVar_hsa_circ_200334,RMVar_hsa_circ_98682,RMVar_hsa_circ_100601,RMVar_hsa_circ_77963,RMVar_hsa_circ_92775,RMVar_hsa_circ_200350,RMVar_hsa_circ_200345,RMVar_hsa_circ_200347,RMVar_hsa_circ_200348,RMVar_hsa_circ_200346,RMVar_hsa_circ_315459,RMVar_hsa_circ_122046,RMVar_hsa_circ_125037,RMVar_hsa_circ_200349,RMVar_hsa_circ_200357,RMVar_hsa_circ_3762,RMVar_hsa_circ_372626,RMVar_hsa_circ_377938,RMVar_hsa_circ_200359,RMVar_hsa_circ_374058,RMVar_hsa_circ_320013,RMVar_hsa_circ_292380,RMVar_hsa_circ_272203,RMVar_hsa_circ_48211,RMVar_hsa_circ_127517,RMVar_hsa_circ_200363,RMVar_hsa_circ_200365,RMVar_hsa_circ_200367,RMVar_hsa_circ_200366,RMVar_hsa_circ_200364,RMVar_hsa_circ_200361,RMVar_hsa_circ_200362,RMVar_hsa_circ_200360,RMVar_hsa_circ_200370,RMVar_hsa_circ_107865,RMVar_hsa_circ_200371,RMVar_hsa_circ_320057,RMVar_hsa_circ_348197,RMVar_hsa_circ_309548,RMVar_hsa_circ_273724,RMVar_hsa_circ_106935,RMVar_hsa_circ_7177,RMVar_hsa_circ_200373,RMVar_hsa_circ_200375,RMVar_hsa_circ_101723,RMVar_hsa_circ_200376,RMVar_hsa_circ_200374,RMVar_hsa_circ_96761,RMVar_hsa_circ_200372,RMVar_hsa_circ_112999,RMVar_hsa_circ_340947,RMVar_hsa_circ_200380,RMVar_hsa_circ_76320,RMVar_hsa_circ_49393,RMVar_hsa_circ_24811,RMVar_hsa_circ_77703,RMVar_hsa_circ_34688,RMVar_hsa_circ_200382,RMVar_hsa_circ_200383,RMVar_hsa_circ_98696,RMVar_hsa_circ_104328,RMVar_hsa_circ_200386,RMVar_hsa_circ_200388,RMVar_hsa_circ_94263,RMVar_hsa_circ_40704,RMVar_hsa_circ_200389,RMVar_hsa_circ_200390,RMVar_hsa_circ_41656,RMVar_hsa_circ_19925,RMVar_hsa_circ_47977,RMVar_hsa_circ_36478,RMVar_hsa_circ_78570,RMVar_hsa_circ_317685,RMVar_hsa_circ_44528,RMVar_hsa_circ_21783,RMVar_hsa_circ_25474,RMVar_hsa_circ_200395,RMVar_hsa_circ_19177,RMVar_hsa_circ_200394,RMVar_hsa_circ_284941,RMVar_hsa_circ_310707,RMVar_hsa_circ_318427,RMVar_hsa_circ_323271,RMVar_hsa_circ_67378,RMVar_hsa_circ_200399,RMVar_hsa_circ_96551,RMVar_hsa_circ_200397,RMVar_hsa_circ_200398,RMVar_hsa_circ_120605,RMVar_hsa_circ_77721,RMVar_hsa_circ_89197,RMVar_hsa_circ_200401,RMVar_hsa_circ_200402,RMVar_hsa_circ_200400 45250 RMVar_ID_45250 Human_SNP_ID_74547316 A-to-I Human chr2 - 61282678 61282678 61282678 ACAAGCGATCCTCTGGCTTCAGCCTCCCAAGTAGCTGGGACCATAGGTGCACATCACCATGCCCA ACAAGCGATCCTCTGGCTTCAGCCTCCCAAGTGGCTGGGACCATAGGTGCACATCACCATGCCCA T C USP34 Ensembl:ENSG00000115464 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1462776347 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_200292,RMVar_hsa_circ_102784,RMVar_hsa_circ_99836,RMVar_hsa_circ_200276,RMVar_hsa_circ_200277,RMVar_hsa_circ_114329,RMVar_hsa_circ_29974,RMVar_hsa_circ_200282,RMVar_hsa_circ_96988,RMVar_hsa_circ_116467,RMVar_hsa_circ_200283,RMVar_hsa_circ_56536,RMVar_hsa_circ_76655,RMVar_hsa_circ_200290,RMVar_hsa_circ_124258,RMVar_hsa_circ_87961,RMVar_hsa_circ_109206,RMVar_hsa_circ_200294,RMVar_hsa_circ_200293,RMVar_hsa_circ_108164,RMVar_hsa_circ_200291,RMVar_hsa_circ_113788,RMVar_hsa_circ_109227,RMVar_hsa_circ_77073,RMVar_hsa_circ_200304,RMVar_hsa_circ_200306,RMVar_hsa_circ_200305,RMVar_hsa_circ_200303,RMVar_hsa_circ_52447,RMVar_hsa_circ_89816,RMVar_hsa_circ_200309,RMVar_hsa_circ_269487,RMVar_hsa_circ_109103,RMVar_hsa_circ_48894,RMVar_hsa_circ_360525,RMVar_hsa_circ_118352,RMVar_hsa_circ_14359,RMVar_hsa_circ_45871,RMVar_hsa_circ_200326,RMVar_hsa_circ_200327,RMVar_hsa_circ_38689,RMVar_hsa_circ_104673,RMVar_hsa_circ_87037,RMVar_hsa_circ_349106,RMVar_hsa_circ_119244,RMVar_hsa_circ_115630,RMVar_hsa_circ_200333,RMVar_hsa_circ_100922,RMVar_hsa_circ_96734,RMVar_hsa_circ_200337,RMVar_hsa_circ_59928,RMVar_hsa_circ_83980,RMVar_hsa_circ_200339,RMVar_hsa_circ_200338,RMVar_hsa_circ_200335,RMVar_hsa_circ_200336,RMVar_hsa_circ_331011,RMVar_hsa_circ_200334,RMVar_hsa_circ_98682,RMVar_hsa_circ_100601,RMVar_hsa_circ_92775,RMVar_hsa_circ_200347,RMVar_hsa_circ_200348,RMVar_hsa_circ_200346,RMVar_hsa_circ_122046,RMVar_hsa_circ_125037,RMVar_hsa_circ_200349,RMVar_hsa_circ_200357,RMVar_hsa_circ_3762,RMVar_hsa_circ_372626,RMVar_hsa_circ_377938,RMVar_hsa_circ_200359,RMVar_hsa_circ_374058,RMVar_hsa_circ_320013,RMVar_hsa_circ_292380,RMVar_hsa_circ_48211,RMVar_hsa_circ_127517,RMVar_hsa_circ_200363,RMVar_hsa_circ_200365,RMVar_hsa_circ_200364,RMVar_hsa_circ_200361,RMVar_hsa_circ_200362,RMVar_hsa_circ_200360,RMVar_hsa_circ_200371,RMVar_hsa_circ_348197,RMVar_hsa_circ_106935,RMVar_hsa_circ_8316,RMVar_hsa_circ_7177,RMVar_hsa_circ_200373,RMVar_hsa_circ_101723,RMVar_hsa_circ_200374,RMVar_hsa_circ_200372,RMVar_hsa_circ_112999,RMVar_hsa_circ_76320,RMVar_hsa_circ_49393,RMVar_hsa_circ_24811,RMVar_hsa_circ_77703,RMVar_hsa_circ_200382,RMVar_hsa_circ_200383,RMVar_hsa_circ_104328,RMVar_hsa_circ_200388,RMVar_hsa_circ_40704,RMVar_hsa_circ_200389,RMVar_hsa_circ_47977,RMVar_hsa_circ_36478,RMVar_hsa_circ_78570,RMVar_hsa_circ_44528,RMVar_hsa_circ_21783,RMVar_hsa_circ_25474,RMVar_hsa_circ_200395,RMVar_hsa_circ_19177,RMVar_hsa_circ_310707,RMVar_hsa_circ_323271,RMVar_hsa_circ_67378,RMVar_hsa_circ_26145,RMVar_hsa_circ_200399,RMVar_hsa_circ_96551,RMVar_hsa_circ_120605,RMVar_hsa_circ_77721,RMVar_hsa_circ_89197,RMVar_hsa_circ_200401,RMVar_hsa_circ_200402,RMVar_hsa_circ_200400,RMVar_hsa_circ_285496,RMVar_hsa_circ_311084,RMVar_hsa_circ_334793,RMVar_hsa_circ_336136,RMVar_hsa_circ_318938,RMVar_hsa_circ_296828,RMVar_hsa_circ_274352,RMVar_hsa_circ_60030,RMVar_hsa_circ_113678,RMVar_hsa_circ_200405,RMVar_hsa_circ_200407,RMVar_hsa_circ_200408,RMVar_hsa_circ_200406,RMVar_hsa_circ_200404,RMVar_hsa_circ_114391,RMVar_hsa_circ_292329,RMVar_hsa_circ_200410,RMVar_hsa_circ_79531,RMVar_hsa_circ_200411,RMVar_hsa_circ_323520,RMVar_hsa_circ_328207,RMVar_hsa_circ_200409,RMVar_hsa_circ_324303,RMVar_hsa_circ_303388,RMVar_hsa_circ_50654,RMVar_hsa_circ_46710,RMVar_hsa_circ_80860,RMVar_hsa_circ_200412,RMVar_hsa_circ_200414,RMVar_hsa_circ_200415,RMVar_hsa_circ_200413,RMVar_hsa_circ_102056,RMVar_hsa_circ_125202,RMVar_hsa_circ_86820,RMVar_hsa_circ_200417,RMVar_hsa_circ_200419,RMVar_hsa_circ_200420,RMVar_hsa_circ_200418 45251 RMVar_ID_45251 Human_SNP_ID_74550801 A-to-I Human chr2 - 61293812 61293812 61293812 TGAGGTCTTCCTATGTTGTCTAGGCTGGTCTCAAAGTCCTAACCTCAAGCCATCGTCTGGCTTTG TGAGGTCTTCCTATGTTGTCTAGGCTGGTCTCGAAGTCCTAACCTCAAGCCATCGTCTGGCTTTG T C USP34 Ensembl:ENSG00000115464 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs944631290 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_200292,RMVar_hsa_circ_102784,RMVar_hsa_circ_99836,RMVar_hsa_circ_200276,RMVar_hsa_circ_200277,RMVar_hsa_circ_114329,RMVar_hsa_circ_200282,RMVar_hsa_circ_96988,RMVar_hsa_circ_116467,RMVar_hsa_circ_200283,RMVar_hsa_circ_56536,RMVar_hsa_circ_76655,RMVar_hsa_circ_200290,RMVar_hsa_circ_124258,RMVar_hsa_circ_87961,RMVar_hsa_circ_109206,RMVar_hsa_circ_200294,RMVar_hsa_circ_200293,RMVar_hsa_circ_108164,RMVar_hsa_circ_200291,RMVar_hsa_circ_113788,RMVar_hsa_circ_109227,RMVar_hsa_circ_200304,RMVar_hsa_circ_200305,RMVar_hsa_circ_200303,RMVar_hsa_circ_89816,RMVar_hsa_circ_200309,RMVar_hsa_circ_109103,RMVar_hsa_circ_118352,RMVar_hsa_circ_14359,RMVar_hsa_circ_45871,RMVar_hsa_circ_200326,RMVar_hsa_circ_200327,RMVar_hsa_circ_38689,RMVar_hsa_circ_104673,RMVar_hsa_circ_87037,RMVar_hsa_circ_119244,RMVar_hsa_circ_200333,RMVar_hsa_circ_96734,RMVar_hsa_circ_200335,RMVar_hsa_circ_200334,RMVar_hsa_circ_98682,RMVar_hsa_circ_100601,RMVar_hsa_circ_92775,RMVar_hsa_circ_200347,RMVar_hsa_circ_200348,RMVar_hsa_circ_122046,RMVar_hsa_circ_125037,RMVar_hsa_circ_200349,RMVar_hsa_circ_200357,RMVar_hsa_circ_3762,RMVar_hsa_circ_372626,RMVar_hsa_circ_377938,RMVar_hsa_circ_200359,RMVar_hsa_circ_374058,RMVar_hsa_circ_292380,RMVar_hsa_circ_127517,RMVar_hsa_circ_200363,RMVar_hsa_circ_200361,RMVar_hsa_circ_200362,RMVar_hsa_circ_200360,RMVar_hsa_circ_200371,RMVar_hsa_circ_348197,RMVar_hsa_circ_106935,RMVar_hsa_circ_7177,RMVar_hsa_circ_200373,RMVar_hsa_circ_200372,RMVar_hsa_circ_112999,RMVar_hsa_circ_76320,RMVar_hsa_circ_49393,RMVar_hsa_circ_24811,RMVar_hsa_circ_77703,RMVar_hsa_circ_200382,RMVar_hsa_circ_200383,RMVar_hsa_circ_104328,RMVar_hsa_circ_200388,RMVar_hsa_circ_40704,RMVar_hsa_circ_200389,RMVar_hsa_circ_47977,RMVar_hsa_circ_36478,RMVar_hsa_circ_78570,RMVar_hsa_circ_200395,RMVar_hsa_circ_19177,RMVar_hsa_circ_67378,RMVar_hsa_circ_26145,RMVar_hsa_circ_200399,RMVar_hsa_circ_96551,RMVar_hsa_circ_120605,RMVar_hsa_circ_77721,RMVar_hsa_circ_89197,RMVar_hsa_circ_200401,RMVar_hsa_circ_200402,RMVar_hsa_circ_200400,RMVar_hsa_circ_311084,RMVar_hsa_circ_336136,RMVar_hsa_circ_318938,RMVar_hsa_circ_296828,RMVar_hsa_circ_60030,RMVar_hsa_circ_113678,RMVar_hsa_circ_200407,RMVar_hsa_circ_200408,RMVar_hsa_circ_200406,RMVar_hsa_circ_114391,RMVar_hsa_circ_292329,RMVar_hsa_circ_200410,RMVar_hsa_circ_79531,RMVar_hsa_circ_200411,RMVar_hsa_circ_323520,RMVar_hsa_circ_328207,RMVar_hsa_circ_200409,RMVar_hsa_circ_50654,RMVar_hsa_circ_46710,RMVar_hsa_circ_24659,RMVar_hsa_circ_80860,RMVar_hsa_circ_200412,RMVar_hsa_circ_200413,RMVar_hsa_circ_102056,RMVar_hsa_circ_125202,RMVar_hsa_circ_86820,RMVar_hsa_circ_200417,RMVar_hsa_circ_200419,RMVar_hsa_circ_200420,RMVar_hsa_circ_200418,RMVar_hsa_circ_106370,RMVar_hsa_circ_270455,RMVar_hsa_circ_324588,RMVar_hsa_circ_200422,RMVar_hsa_circ_328280,RMVar_hsa_circ_351952,RMVar_hsa_circ_302551,RMVar_hsa_circ_317971,RMVar_hsa_circ_73252,RMVar_hsa_circ_117262,RMVar_hsa_circ_51386,RMVar_hsa_circ_6136,RMVar_hsa_circ_200426,RMVar_hsa_circ_200428,RMVar_hsa_circ_11160,RMVar_hsa_circ_200427,RMVar_hsa_circ_200424,RMVar_hsa_circ_200425,RMVar_hsa_circ_200431,RMVar_hsa_circ_370826,RMVar_hsa_circ_200423,RMVar_hsa_circ_287543,RMVar_hsa_circ_352751,RMVar_hsa_circ_200430,RMVar_hsa_circ_319338,RMVar_hsa_circ_5525 45252 RMVar_ID_45252 Human_SNP_ID_74550967 A-to-I Human chr2 - 61294270 61294270 61294270 GCGATCTCTGCTTGCTGCAAGCTCCGCCTCCCAGGTTCACGCGATTCTCCTGCCTCAGCCTCTGG GCGATCTCTGCTTGCTGCAAGCTCCGCCTCCCGGGTTCACGCGATTCTCCTGCCTCAGCCTCTGG T C USP34 Ensembl:ENSG00000115464 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1224942436 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_200292,RMVar_hsa_circ_102784,RMVar_hsa_circ_99836,RMVar_hsa_circ_200276,RMVar_hsa_circ_200277,RMVar_hsa_circ_114329,RMVar_hsa_circ_200282,RMVar_hsa_circ_96988,RMVar_hsa_circ_116467,RMVar_hsa_circ_200283,RMVar_hsa_circ_56536,RMVar_hsa_circ_76655,RMVar_hsa_circ_200290,RMVar_hsa_circ_124258,RMVar_hsa_circ_87961,RMVar_hsa_circ_109206,RMVar_hsa_circ_200294,RMVar_hsa_circ_200293,RMVar_hsa_circ_108164,RMVar_hsa_circ_200291,RMVar_hsa_circ_113788,RMVar_hsa_circ_109227,RMVar_hsa_circ_200304,RMVar_hsa_circ_200305,RMVar_hsa_circ_200303,RMVar_hsa_circ_89816,RMVar_hsa_circ_200309,RMVar_hsa_circ_109103,RMVar_hsa_circ_118352,RMVar_hsa_circ_14359,RMVar_hsa_circ_45871,RMVar_hsa_circ_200326,RMVar_hsa_circ_200327,RMVar_hsa_circ_38689,RMVar_hsa_circ_104673,RMVar_hsa_circ_87037,RMVar_hsa_circ_119244,RMVar_hsa_circ_200333,RMVar_hsa_circ_96734,RMVar_hsa_circ_200335,RMVar_hsa_circ_200334,RMVar_hsa_circ_98682,RMVar_hsa_circ_100601,RMVar_hsa_circ_92775,RMVar_hsa_circ_200347,RMVar_hsa_circ_200348,RMVar_hsa_circ_122046,RMVar_hsa_circ_125037,RMVar_hsa_circ_200349,RMVar_hsa_circ_200357,RMVar_hsa_circ_3762,RMVar_hsa_circ_372626,RMVar_hsa_circ_377938,RMVar_hsa_circ_200359,RMVar_hsa_circ_374058,RMVar_hsa_circ_292380,RMVar_hsa_circ_127517,RMVar_hsa_circ_200363,RMVar_hsa_circ_200361,RMVar_hsa_circ_200362,RMVar_hsa_circ_200360,RMVar_hsa_circ_200371,RMVar_hsa_circ_348197,RMVar_hsa_circ_106935,RMVar_hsa_circ_7177,RMVar_hsa_circ_200373,RMVar_hsa_circ_200372,RMVar_hsa_circ_112999,RMVar_hsa_circ_76320,RMVar_hsa_circ_49393,RMVar_hsa_circ_24811,RMVar_hsa_circ_77703,RMVar_hsa_circ_200382,RMVar_hsa_circ_200383,RMVar_hsa_circ_104328,RMVar_hsa_circ_200388,RMVar_hsa_circ_40704,RMVar_hsa_circ_200389,RMVar_hsa_circ_47977,RMVar_hsa_circ_36478,RMVar_hsa_circ_78570,RMVar_hsa_circ_200395,RMVar_hsa_circ_19177,RMVar_hsa_circ_67378,RMVar_hsa_circ_26145,RMVar_hsa_circ_200399,RMVar_hsa_circ_96551,RMVar_hsa_circ_120605,RMVar_hsa_circ_77721,RMVar_hsa_circ_89197,RMVar_hsa_circ_200401,RMVar_hsa_circ_200402,RMVar_hsa_circ_200400,RMVar_hsa_circ_311084,RMVar_hsa_circ_336136,RMVar_hsa_circ_318938,RMVar_hsa_circ_296828,RMVar_hsa_circ_60030,RMVar_hsa_circ_113678,RMVar_hsa_circ_200407,RMVar_hsa_circ_200408,RMVar_hsa_circ_200406,RMVar_hsa_circ_114391,RMVar_hsa_circ_292329,RMVar_hsa_circ_200410,RMVar_hsa_circ_79531,RMVar_hsa_circ_200411,RMVar_hsa_circ_323520,RMVar_hsa_circ_328207,RMVar_hsa_circ_200409,RMVar_hsa_circ_50654,RMVar_hsa_circ_46710,RMVar_hsa_circ_24659,RMVar_hsa_circ_80860,RMVar_hsa_circ_200412,RMVar_hsa_circ_200413,RMVar_hsa_circ_102056,RMVar_hsa_circ_125202,RMVar_hsa_circ_86820,RMVar_hsa_circ_200417,RMVar_hsa_circ_200419,RMVar_hsa_circ_200420,RMVar_hsa_circ_200418,RMVar_hsa_circ_106370,RMVar_hsa_circ_270455,RMVar_hsa_circ_324588,RMVar_hsa_circ_200422,RMVar_hsa_circ_328280,RMVar_hsa_circ_351952,RMVar_hsa_circ_302551,RMVar_hsa_circ_317971,RMVar_hsa_circ_73252,RMVar_hsa_circ_117262,RMVar_hsa_circ_51386,RMVar_hsa_circ_6136,RMVar_hsa_circ_200426,RMVar_hsa_circ_200428,RMVar_hsa_circ_11160,RMVar_hsa_circ_200427,RMVar_hsa_circ_200424,RMVar_hsa_circ_200425,RMVar_hsa_circ_200431,RMVar_hsa_circ_370826,RMVar_hsa_circ_200423,RMVar_hsa_circ_287543,RMVar_hsa_circ_352751,RMVar_hsa_circ_200430,RMVar_hsa_circ_319338,RMVar_hsa_circ_5525 45253 RMVar_ID_45253 Human_SNP_ID_74551060 A-to-I Human chr2 - 61294479 61294479 61294479 AGGAGGTGGAGGTTGCAGTGAGCTGAGATCGCACCACAGCACTCCAGCCTGGGCAGCAAAAAAAA AGGAGGTGGAGGTTGCAGTGAGCTGAGATCGCGCCACAGCACTCCAGCCTGGGCAGCAAAAAAAA T C USP34 Ensembl:ENSG00000115464 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs765257333 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_200292,RMVar_hsa_circ_102784,RMVar_hsa_circ_99836,RMVar_hsa_circ_200276,RMVar_hsa_circ_200277,RMVar_hsa_circ_114329,RMVar_hsa_circ_200282,RMVar_hsa_circ_96988,RMVar_hsa_circ_116467,RMVar_hsa_circ_200283,RMVar_hsa_circ_56536,RMVar_hsa_circ_76655,RMVar_hsa_circ_200290,RMVar_hsa_circ_124258,RMVar_hsa_circ_87961,RMVar_hsa_circ_109206,RMVar_hsa_circ_200294,RMVar_hsa_circ_200293,RMVar_hsa_circ_108164,RMVar_hsa_circ_200291,RMVar_hsa_circ_113788,RMVar_hsa_circ_109227,RMVar_hsa_circ_200304,RMVar_hsa_circ_200305,RMVar_hsa_circ_200303,RMVar_hsa_circ_89816,RMVar_hsa_circ_200309,RMVar_hsa_circ_109103,RMVar_hsa_circ_118352,RMVar_hsa_circ_14359,RMVar_hsa_circ_45871,RMVar_hsa_circ_200326,RMVar_hsa_circ_200327,RMVar_hsa_circ_38689,RMVar_hsa_circ_104673,RMVar_hsa_circ_87037,RMVar_hsa_circ_119244,RMVar_hsa_circ_200333,RMVar_hsa_circ_96734,RMVar_hsa_circ_200335,RMVar_hsa_circ_200334,RMVar_hsa_circ_98682,RMVar_hsa_circ_100601,RMVar_hsa_circ_92775,RMVar_hsa_circ_200347,RMVar_hsa_circ_200348,RMVar_hsa_circ_122046,RMVar_hsa_circ_125037,RMVar_hsa_circ_200349,RMVar_hsa_circ_200357,RMVar_hsa_circ_3762,RMVar_hsa_circ_372626,RMVar_hsa_circ_377938,RMVar_hsa_circ_200359,RMVar_hsa_circ_374058,RMVar_hsa_circ_292380,RMVar_hsa_circ_127517,RMVar_hsa_circ_200363,RMVar_hsa_circ_200361,RMVar_hsa_circ_200362,RMVar_hsa_circ_200360,RMVar_hsa_circ_200371,RMVar_hsa_circ_348197,RMVar_hsa_circ_106935,RMVar_hsa_circ_7177,RMVar_hsa_circ_200373,RMVar_hsa_circ_200372,RMVar_hsa_circ_112999,RMVar_hsa_circ_76320,RMVar_hsa_circ_49393,RMVar_hsa_circ_24811,RMVar_hsa_circ_77703,RMVar_hsa_circ_200382,RMVar_hsa_circ_200383,RMVar_hsa_circ_104328,RMVar_hsa_circ_200388,RMVar_hsa_circ_40704,RMVar_hsa_circ_200389,RMVar_hsa_circ_47977,RMVar_hsa_circ_36478,RMVar_hsa_circ_78570,RMVar_hsa_circ_200395,RMVar_hsa_circ_19177,RMVar_hsa_circ_67378,RMVar_hsa_circ_26145,RMVar_hsa_circ_200399,RMVar_hsa_circ_96551,RMVar_hsa_circ_120605,RMVar_hsa_circ_77721,RMVar_hsa_circ_89197,RMVar_hsa_circ_200401,RMVar_hsa_circ_200402,RMVar_hsa_circ_200400,RMVar_hsa_circ_311084,RMVar_hsa_circ_336136,RMVar_hsa_circ_318938,RMVar_hsa_circ_296828,RMVar_hsa_circ_60030,RMVar_hsa_circ_113678,RMVar_hsa_circ_200407,RMVar_hsa_circ_200408,RMVar_hsa_circ_200406,RMVar_hsa_circ_114391,RMVar_hsa_circ_292329,RMVar_hsa_circ_200410,RMVar_hsa_circ_79531,RMVar_hsa_circ_200411,RMVar_hsa_circ_323520,RMVar_hsa_circ_328207,RMVar_hsa_circ_200409,RMVar_hsa_circ_50654,RMVar_hsa_circ_46710,RMVar_hsa_circ_24659,RMVar_hsa_circ_80860,RMVar_hsa_circ_200412,RMVar_hsa_circ_200413,RMVar_hsa_circ_102056,RMVar_hsa_circ_125202,RMVar_hsa_circ_86820,RMVar_hsa_circ_200417,RMVar_hsa_circ_200419,RMVar_hsa_circ_200420,RMVar_hsa_circ_200418,RMVar_hsa_circ_106370,RMVar_hsa_circ_270455,RMVar_hsa_circ_324588,RMVar_hsa_circ_200422,RMVar_hsa_circ_328280,RMVar_hsa_circ_351952,RMVar_hsa_circ_302551,RMVar_hsa_circ_317971,RMVar_hsa_circ_73252,RMVar_hsa_circ_117262,RMVar_hsa_circ_51386,RMVar_hsa_circ_6136,RMVar_hsa_circ_200426,RMVar_hsa_circ_200428,RMVar_hsa_circ_11160,RMVar_hsa_circ_200427,RMVar_hsa_circ_200424,RMVar_hsa_circ_200425,RMVar_hsa_circ_200431,RMVar_hsa_circ_370826,RMVar_hsa_circ_200423,RMVar_hsa_circ_287543,RMVar_hsa_circ_352751,RMVar_hsa_circ_200430,RMVar_hsa_circ_319338,RMVar_hsa_circ_5525 45254 RMVar_ID_45254 Human_SNP_ID_74551061 A-to-I Human chr2 - 61294479 61294479 61294479 AGGAGGTGGAGGTTGCAGTGAGCTGAGATCGCACCACAGCACTCCAGCCTGGGCAGCAAAAAAAA AGGAGGTGGAGGTTGCAGTGAGCTGAGATCGCCCCACAGCACTCCAGCCTGGGCAGCAAAAAAAA T G USP34 Ensembl:ENSG00000115464 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs765257333 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_200292,RMVar_hsa_circ_102784,RMVar_hsa_circ_99836,RMVar_hsa_circ_200276,RMVar_hsa_circ_200277,RMVar_hsa_circ_114329,RMVar_hsa_circ_200282,RMVar_hsa_circ_96988,RMVar_hsa_circ_116467,RMVar_hsa_circ_200283,RMVar_hsa_circ_56536,RMVar_hsa_circ_76655,RMVar_hsa_circ_200290,RMVar_hsa_circ_124258,RMVar_hsa_circ_87961,RMVar_hsa_circ_109206,RMVar_hsa_circ_200294,RMVar_hsa_circ_200293,RMVar_hsa_circ_108164,RMVar_hsa_circ_200291,RMVar_hsa_circ_113788,RMVar_hsa_circ_109227,RMVar_hsa_circ_200304,RMVar_hsa_circ_200305,RMVar_hsa_circ_200303,RMVar_hsa_circ_89816,RMVar_hsa_circ_200309,RMVar_hsa_circ_109103,RMVar_hsa_circ_118352,RMVar_hsa_circ_14359,RMVar_hsa_circ_45871,RMVar_hsa_circ_200326,RMVar_hsa_circ_200327,RMVar_hsa_circ_38689,RMVar_hsa_circ_104673,RMVar_hsa_circ_87037,RMVar_hsa_circ_119244,RMVar_hsa_circ_200333,RMVar_hsa_circ_96734,RMVar_hsa_circ_200335,RMVar_hsa_circ_200334,RMVar_hsa_circ_98682,RMVar_hsa_circ_100601,RMVar_hsa_circ_92775,RMVar_hsa_circ_200347,RMVar_hsa_circ_200348,RMVar_hsa_circ_122046,RMVar_hsa_circ_125037,RMVar_hsa_circ_200349,RMVar_hsa_circ_200357,RMVar_hsa_circ_3762,RMVar_hsa_circ_372626,RMVar_hsa_circ_377938,RMVar_hsa_circ_200359,RMVar_hsa_circ_374058,RMVar_hsa_circ_292380,RMVar_hsa_circ_127517,RMVar_hsa_circ_200363,RMVar_hsa_circ_200361,RMVar_hsa_circ_200362,RMVar_hsa_circ_200360,RMVar_hsa_circ_200371,RMVar_hsa_circ_348197,RMVar_hsa_circ_106935,RMVar_hsa_circ_7177,RMVar_hsa_circ_200373,RMVar_hsa_circ_200372,RMVar_hsa_circ_112999,RMVar_hsa_circ_76320,RMVar_hsa_circ_49393,RMVar_hsa_circ_24811,RMVar_hsa_circ_77703,RMVar_hsa_circ_200382,RMVar_hsa_circ_200383,RMVar_hsa_circ_104328,RMVar_hsa_circ_200388,RMVar_hsa_circ_40704,RMVar_hsa_circ_200389,RMVar_hsa_circ_47977,RMVar_hsa_circ_36478,RMVar_hsa_circ_78570,RMVar_hsa_circ_200395,RMVar_hsa_circ_19177,RMVar_hsa_circ_67378,RMVar_hsa_circ_26145,RMVar_hsa_circ_200399,RMVar_hsa_circ_96551,RMVar_hsa_circ_120605,RMVar_hsa_circ_77721,RMVar_hsa_circ_89197,RMVar_hsa_circ_200401,RMVar_hsa_circ_200402,RMVar_hsa_circ_200400,RMVar_hsa_circ_311084,RMVar_hsa_circ_336136,RMVar_hsa_circ_318938,RMVar_hsa_circ_296828,RMVar_hsa_circ_60030,RMVar_hsa_circ_113678,RMVar_hsa_circ_200407,RMVar_hsa_circ_200408,RMVar_hsa_circ_200406,RMVar_hsa_circ_114391,RMVar_hsa_circ_292329,RMVar_hsa_circ_200410,RMVar_hsa_circ_79531,RMVar_hsa_circ_200411,RMVar_hsa_circ_323520,RMVar_hsa_circ_328207,RMVar_hsa_circ_200409,RMVar_hsa_circ_50654,RMVar_hsa_circ_46710,RMVar_hsa_circ_24659,RMVar_hsa_circ_80860,RMVar_hsa_circ_200412,RMVar_hsa_circ_200413,RMVar_hsa_circ_102056,RMVar_hsa_circ_125202,RMVar_hsa_circ_86820,RMVar_hsa_circ_200417,RMVar_hsa_circ_200419,RMVar_hsa_circ_200420,RMVar_hsa_circ_200418,RMVar_hsa_circ_106370,RMVar_hsa_circ_270455,RMVar_hsa_circ_324588,RMVar_hsa_circ_200422,RMVar_hsa_circ_328280,RMVar_hsa_circ_351952,RMVar_hsa_circ_302551,RMVar_hsa_circ_317971,RMVar_hsa_circ_73252,RMVar_hsa_circ_117262,RMVar_hsa_circ_51386,RMVar_hsa_circ_6136,RMVar_hsa_circ_200426,RMVar_hsa_circ_200428,RMVar_hsa_circ_11160,RMVar_hsa_circ_200427,RMVar_hsa_circ_200424,RMVar_hsa_circ_200425,RMVar_hsa_circ_200431,RMVar_hsa_circ_370826,RMVar_hsa_circ_200423,RMVar_hsa_circ_287543,RMVar_hsa_circ_352751,RMVar_hsa_circ_200430,RMVar_hsa_circ_319338,RMVar_hsa_circ_5525 45255 RMVar_ID_45255 Human_SNP_ID_74558260 A-to-I Human chr2 - 61316159 61316159 61316159 CACTCTGATAACTGCTGGAGTGCAGTGGCACAATCTTGGCTCACTGCAACCTCCGCCTCCCAGGT CACTCTGATAACTGCTGGAGTGCAGTGGCACAGTCTTGGCTCACTGCAACCTCCGCCTCCCAGGT T C USP34 Ensembl:ENSG00000115464 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs921711299 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_200292,RMVar_hsa_circ_102784,RMVar_hsa_circ_99836,RMVar_hsa_circ_200276,RMVar_hsa_circ_200277,RMVar_hsa_circ_114329,RMVar_hsa_circ_200282,RMVar_hsa_circ_96988,RMVar_hsa_circ_200283,RMVar_hsa_circ_124258,RMVar_hsa_circ_87961,RMVar_hsa_circ_109206,RMVar_hsa_circ_200293,RMVar_hsa_circ_200291,RMVar_hsa_circ_113788,RMVar_hsa_circ_109227,RMVar_hsa_circ_200304,RMVar_hsa_circ_200303,RMVar_hsa_circ_89816,RMVar_hsa_circ_200309,RMVar_hsa_circ_109103,RMVar_hsa_circ_118352,RMVar_hsa_circ_14359,RMVar_hsa_circ_200326,RMVar_hsa_circ_200327,RMVar_hsa_circ_38689,RMVar_hsa_circ_119244,RMVar_hsa_circ_200333,RMVar_hsa_circ_96734,RMVar_hsa_circ_200334,RMVar_hsa_circ_98682,RMVar_hsa_circ_100601,RMVar_hsa_circ_92775,RMVar_hsa_circ_200347,RMVar_hsa_circ_200348,RMVar_hsa_circ_122046,RMVar_hsa_circ_200349,RMVar_hsa_circ_3762,RMVar_hsa_circ_377938,RMVar_hsa_circ_200359,RMVar_hsa_circ_374058,RMVar_hsa_circ_127517,RMVar_hsa_circ_200360,RMVar_hsa_circ_200371,RMVar_hsa_circ_106935,RMVar_hsa_circ_34337,RMVar_hsa_circ_7177,RMVar_hsa_circ_200372,RMVar_hsa_circ_112999,RMVar_hsa_circ_76320,RMVar_hsa_circ_77703,RMVar_hsa_circ_200382,RMVar_hsa_circ_200383,RMVar_hsa_circ_104328,RMVar_hsa_circ_200388,RMVar_hsa_circ_40704,RMVar_hsa_circ_200389,RMVar_hsa_circ_78570,RMVar_hsa_circ_200395,RMVar_hsa_circ_19177,RMVar_hsa_circ_67378,RMVar_hsa_circ_200399,RMVar_hsa_circ_96551,RMVar_hsa_circ_120605,RMVar_hsa_circ_77721,RMVar_hsa_circ_200401,RMVar_hsa_circ_200400,RMVar_hsa_circ_336136,RMVar_hsa_circ_296828,RMVar_hsa_circ_60030,RMVar_hsa_circ_113678,RMVar_hsa_circ_200407,RMVar_hsa_circ_200408,RMVar_hsa_circ_114391,RMVar_hsa_circ_200410,RMVar_hsa_circ_79531,RMVar_hsa_circ_200411,RMVar_hsa_circ_323520,RMVar_hsa_circ_328207,RMVar_hsa_circ_200409,RMVar_hsa_circ_24659,RMVar_hsa_circ_200412,RMVar_hsa_circ_102056,RMVar_hsa_circ_125202,RMVar_hsa_circ_86820,RMVar_hsa_circ_200419,RMVar_hsa_circ_200420,RMVar_hsa_circ_200418,RMVar_hsa_circ_106370,RMVar_hsa_circ_200422,RMVar_hsa_circ_328280,RMVar_hsa_circ_351952,RMVar_hsa_circ_317971,RMVar_hsa_circ_73252,RMVar_hsa_circ_117262,RMVar_hsa_circ_51386,RMVar_hsa_circ_6136,RMVar_hsa_circ_200424,RMVar_hsa_circ_200425,RMVar_hsa_circ_200431,RMVar_hsa_circ_370826,RMVar_hsa_circ_200423,RMVar_hsa_circ_319338,RMVar_hsa_circ_98377,RMVar_hsa_circ_30797,RMVar_hsa_circ_62411,RMVar_hsa_circ_200434,RMVar_hsa_circ_200432,RMVar_hsa_circ_200433,RMVar_hsa_circ_114277,RMVar_hsa_circ_116290,RMVar_hsa_circ_346875,RMVar_hsa_circ_329354,RMVar_hsa_circ_67986,RMVar_hsa_circ_266880,RMVar_hsa_circ_330411,RMVar_hsa_circ_200435,RMVar_hsa_circ_365268,RMVar_hsa_circ_313314,RMVar_hsa_circ_97100,RMVar_hsa_circ_106675,RMVar_hsa_circ_568,RMVar_hsa_circ_200437,RMVar_hsa_circ_200439,RMVar_hsa_circ_200440,RMVar_hsa_circ_200438,RMVar_hsa_circ_341466,RMVar_hsa_circ_367162,RMVar_hsa_circ_200436,RMVar_hsa_circ_352601,RMVar_hsa_circ_292017,RMVar_hsa_circ_294944,RMVar_hsa_circ_267515,RMVar_hsa_circ_31336,RMVar_hsa_circ_8707,RMVar_hsa_circ_3761,RMVar_hsa_circ_117913,RMVar_hsa_circ_200445,RMVar_hsa_circ_200446,RMVar_hsa_circ_108413,RMVar_hsa_circ_268696,RMVar_hsa_circ_350272,RMVar_hsa_circ_200447,RMVar_hsa_circ_269731,RMVar_hsa_circ_200448,RMVar_hsa_circ_77627,RMVar_hsa_circ_200452 45256 RMVar_ID_45256 Human_SNP_ID_74558347 A-to-I Human chr2 - 61316388 61316388 61316388 TAGAGTTGGGTTTTCACCACGTTGACCAGACTAGTCTCGAACTCCTGACCTCAAGTTTTCCACCC TAGAGTTGGGTTTTCACCACGTTGACCAGACTGGTCTCGAACTCCTGACCTCAAGTTTTCCACCC T C USP34 Ensembl:ENSG00000115464 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1241341550 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13927953 RMVar_hsa_circ_200292,RMVar_hsa_circ_102784,RMVar_hsa_circ_99836,RMVar_hsa_circ_200276,RMVar_hsa_circ_200277,RMVar_hsa_circ_114329,RMVar_hsa_circ_200282,RMVar_hsa_circ_96988,RMVar_hsa_circ_200283,RMVar_hsa_circ_124258,RMVar_hsa_circ_87961,RMVar_hsa_circ_109206,RMVar_hsa_circ_200293,RMVar_hsa_circ_200291,RMVar_hsa_circ_113788,RMVar_hsa_circ_109227,RMVar_hsa_circ_200304,RMVar_hsa_circ_200303,RMVar_hsa_circ_89816,RMVar_hsa_circ_200309,RMVar_hsa_circ_109103,RMVar_hsa_circ_118352,RMVar_hsa_circ_14359,RMVar_hsa_circ_200326,RMVar_hsa_circ_200327,RMVar_hsa_circ_38689,RMVar_hsa_circ_119244,RMVar_hsa_circ_200333,RMVar_hsa_circ_96734,RMVar_hsa_circ_200334,RMVar_hsa_circ_98682,RMVar_hsa_circ_100601,RMVar_hsa_circ_92775,RMVar_hsa_circ_200347,RMVar_hsa_circ_200348,RMVar_hsa_circ_122046,RMVar_hsa_circ_200349,RMVar_hsa_circ_3762,RMVar_hsa_circ_377938,RMVar_hsa_circ_200359,RMVar_hsa_circ_374058,RMVar_hsa_circ_127517,RMVar_hsa_circ_200360,RMVar_hsa_circ_200371,RMVar_hsa_circ_106935,RMVar_hsa_circ_34337,RMVar_hsa_circ_7177,RMVar_hsa_circ_200372,RMVar_hsa_circ_112999,RMVar_hsa_circ_76320,RMVar_hsa_circ_77703,RMVar_hsa_circ_200382,RMVar_hsa_circ_200383,RMVar_hsa_circ_104328,RMVar_hsa_circ_200388,RMVar_hsa_circ_40704,RMVar_hsa_circ_200389,RMVar_hsa_circ_78570,RMVar_hsa_circ_200395,RMVar_hsa_circ_19177,RMVar_hsa_circ_67378,RMVar_hsa_circ_200399,RMVar_hsa_circ_96551,RMVar_hsa_circ_120605,RMVar_hsa_circ_77721,RMVar_hsa_circ_200401,RMVar_hsa_circ_200400,RMVar_hsa_circ_336136,RMVar_hsa_circ_296828,RMVar_hsa_circ_60030,RMVar_hsa_circ_113678,RMVar_hsa_circ_200407,RMVar_hsa_circ_200408,RMVar_hsa_circ_114391,RMVar_hsa_circ_200410,RMVar_hsa_circ_79531,RMVar_hsa_circ_200411,RMVar_hsa_circ_323520,RMVar_hsa_circ_328207,RMVar_hsa_circ_200409,RMVar_hsa_circ_24659,RMVar_hsa_circ_200412,RMVar_hsa_circ_102056,RMVar_hsa_circ_125202,RMVar_hsa_circ_86820,RMVar_hsa_circ_200419,RMVar_hsa_circ_200420,RMVar_hsa_circ_200418,RMVar_hsa_circ_106370,RMVar_hsa_circ_200422,RMVar_hsa_circ_328280,RMVar_hsa_circ_351952,RMVar_hsa_circ_317971,RMVar_hsa_circ_73252,RMVar_hsa_circ_117262,RMVar_hsa_circ_51386,RMVar_hsa_circ_6136,RMVar_hsa_circ_200424,RMVar_hsa_circ_200425,RMVar_hsa_circ_200431,RMVar_hsa_circ_370826,RMVar_hsa_circ_200423,RMVar_hsa_circ_319338,RMVar_hsa_circ_98377,RMVar_hsa_circ_30797,RMVar_hsa_circ_62411,RMVar_hsa_circ_200434,RMVar_hsa_circ_200432,RMVar_hsa_circ_200433,RMVar_hsa_circ_114277,RMVar_hsa_circ_116290,RMVar_hsa_circ_346875,RMVar_hsa_circ_329354,RMVar_hsa_circ_67986,RMVar_hsa_circ_266880,RMVar_hsa_circ_330411,RMVar_hsa_circ_200435,RMVar_hsa_circ_365268,RMVar_hsa_circ_313314,RMVar_hsa_circ_97100,RMVar_hsa_circ_106675,RMVar_hsa_circ_568,RMVar_hsa_circ_200437,RMVar_hsa_circ_200439,RMVar_hsa_circ_200440,RMVar_hsa_circ_200438,RMVar_hsa_circ_341466,RMVar_hsa_circ_367162,RMVar_hsa_circ_200436,RMVar_hsa_circ_352601,RMVar_hsa_circ_292017,RMVar_hsa_circ_294944,RMVar_hsa_circ_267515,RMVar_hsa_circ_31336,RMVar_hsa_circ_8707,RMVar_hsa_circ_3761,RMVar_hsa_circ_117913,RMVar_hsa_circ_200445,RMVar_hsa_circ_200446,RMVar_hsa_circ_108413,RMVar_hsa_circ_268696,RMVar_hsa_circ_350272,RMVar_hsa_circ_200447,RMVar_hsa_circ_269731,RMVar_hsa_circ_200448,RMVar_hsa_circ_77627,RMVar_hsa_circ_200452 45257 RMVar_ID_45257 Human_SNP_ID_74564522 A-to-I Human chr2 - 61336212 61336212 61336212 CTGAGGTGGGAAGTCAAGGCTGCAGTGAGCCAAGATCGCACCACTGCACTCCAGCCTGAGCAACA CTGAGGTGGGAAGTCAAGGCTGCAGTGAGCCAGGATCGCACCACTGCACTCCAGCCTGAGCAACA T C USP34 Ensembl:ENSG00000115464 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1022734491 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_200292,RMVar_hsa_circ_102784,RMVar_hsa_circ_99836,RMVar_hsa_circ_200276,RMVar_hsa_circ_200277,RMVar_hsa_circ_114329,RMVar_hsa_circ_200282,RMVar_hsa_circ_96988,RMVar_hsa_circ_200283,RMVar_hsa_circ_124258,RMVar_hsa_circ_109206,RMVar_hsa_circ_200291,RMVar_hsa_circ_113788,RMVar_hsa_circ_109227,RMVar_hsa_circ_200304,RMVar_hsa_circ_200303,RMVar_hsa_circ_89816,RMVar_hsa_circ_200309,RMVar_hsa_circ_118352,RMVar_hsa_circ_14359,RMVar_hsa_circ_200327,RMVar_hsa_circ_119244,RMVar_hsa_circ_200333,RMVar_hsa_circ_96734,RMVar_hsa_circ_200334,RMVar_hsa_circ_98682,RMVar_hsa_circ_100601,RMVar_hsa_circ_92775,RMVar_hsa_circ_200347,RMVar_hsa_circ_200348,RMVar_hsa_circ_122046,RMVar_hsa_circ_200349,RMVar_hsa_circ_3762,RMVar_hsa_circ_200359,RMVar_hsa_circ_374058,RMVar_hsa_circ_127517,RMVar_hsa_circ_200360,RMVar_hsa_circ_200371,RMVar_hsa_circ_106935,RMVar_hsa_circ_34337,RMVar_hsa_circ_200372,RMVar_hsa_circ_112999,RMVar_hsa_circ_76320,RMVar_hsa_circ_77703,RMVar_hsa_circ_200382,RMVar_hsa_circ_200383,RMVar_hsa_circ_104328,RMVar_hsa_circ_200388,RMVar_hsa_circ_40704,RMVar_hsa_circ_200389,RMVar_hsa_circ_78570,RMVar_hsa_circ_200395,RMVar_hsa_circ_67378,RMVar_hsa_circ_200399,RMVar_hsa_circ_120605,RMVar_hsa_circ_77721,RMVar_hsa_circ_200400,RMVar_hsa_circ_296828,RMVar_hsa_circ_60030,RMVar_hsa_circ_113678,RMVar_hsa_circ_200408,RMVar_hsa_circ_114391,RMVar_hsa_circ_200410,RMVar_hsa_circ_79531,RMVar_hsa_circ_200411,RMVar_hsa_circ_323520,RMVar_hsa_circ_200409,RMVar_hsa_circ_24659,RMVar_hsa_circ_200412,RMVar_hsa_circ_102056,RMVar_hsa_circ_125202,RMVar_hsa_circ_200419,RMVar_hsa_circ_200420,RMVar_hsa_circ_106370,RMVar_hsa_circ_200422,RMVar_hsa_circ_328280,RMVar_hsa_circ_351952,RMVar_hsa_circ_117262,RMVar_hsa_circ_200424,RMVar_hsa_circ_200431,RMVar_hsa_circ_370826,RMVar_hsa_circ_200423,RMVar_hsa_circ_319338,RMVar_hsa_circ_98377,RMVar_hsa_circ_62411,RMVar_hsa_circ_200434,RMVar_hsa_circ_200433,RMVar_hsa_circ_114277,RMVar_hsa_circ_116290,RMVar_hsa_circ_67986,RMVar_hsa_circ_200435,RMVar_hsa_circ_313314,RMVar_hsa_circ_97100,RMVar_hsa_circ_106675,RMVar_hsa_circ_2773,RMVar_hsa_circ_200437,RMVar_hsa_circ_200438,RMVar_hsa_circ_200436,RMVar_hsa_circ_352601,RMVar_hsa_circ_292017,RMVar_hsa_circ_267515,RMVar_hsa_circ_31336,RMVar_hsa_circ_8707,RMVar_hsa_circ_117913,RMVar_hsa_circ_200446,RMVar_hsa_circ_108413,RMVar_hsa_circ_268696,RMVar_hsa_circ_350272,RMVar_hsa_circ_200447,RMVar_hsa_circ_269731,RMVar_hsa_circ_200448,RMVar_hsa_circ_77627,RMVar_hsa_circ_2653,RMVar_hsa_circ_69736,RMVar_hsa_circ_200452,RMVar_hsa_circ_200454,RMVar_hsa_circ_8913,RMVar_hsa_circ_200462,RMVar_hsa_circ_32279,RMVar_hsa_circ_200457,RMVar_hsa_circ_283666,RMVar_hsa_circ_200456,RMVar_hsa_circ_291020,RMVar_hsa_circ_289548,RMVar_hsa_circ_24521,RMVar_hsa_circ_44631,RMVar_hsa_circ_200459,RMVar_hsa_circ_200458,RMVar_hsa_circ_74040,RMVar_hsa_circ_270121,RMVar_hsa_circ_358472,RMVar_hsa_circ_367224,RMVar_hsa_circ_102290,RMVar_hsa_circ_73133,RMVar_hsa_circ_7884,RMVar_hsa_circ_11256,RMVar_hsa_circ_200463,RMVar_hsa_circ_200464,RMVar_hsa_circ_200461,RMVar_hsa_circ_377081 45258 RMVar_ID_45258 Human_SNP_ID_74564550 A-to-I Human chr2 - 61336326 61336325 61336327 GCCCAGTAGTTTGAGACCAGCCTTGGAAACATAGGAAGACCCCATCTCTACAGAAAAACTTTAAA GCCCAGTAGTTTGAGACCAGCCTTGGAAACA__GGAAGACCCCATCTCTACAGAAAAACTTTAAA CTA C USP34 Ensembl:ENSG00000115464 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs962435016 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_25554779 RMVar_hsa_circ_200292,RMVar_hsa_circ_102784,RMVar_hsa_circ_99836,RMVar_hsa_circ_200276,RMVar_hsa_circ_200277,RMVar_hsa_circ_114329,RMVar_hsa_circ_200282,RMVar_hsa_circ_96988,RMVar_hsa_circ_200283,RMVar_hsa_circ_124258,RMVar_hsa_circ_109206,RMVar_hsa_circ_200291,RMVar_hsa_circ_113788,RMVar_hsa_circ_109227,RMVar_hsa_circ_200304,RMVar_hsa_circ_200303,RMVar_hsa_circ_89816,RMVar_hsa_circ_200309,RMVar_hsa_circ_118352,RMVar_hsa_circ_14359,RMVar_hsa_circ_200327,RMVar_hsa_circ_119244,RMVar_hsa_circ_200333,RMVar_hsa_circ_96734,RMVar_hsa_circ_200334,RMVar_hsa_circ_98682,RMVar_hsa_circ_100601,RMVar_hsa_circ_92775,RMVar_hsa_circ_200347,RMVar_hsa_circ_200348,RMVar_hsa_circ_122046,RMVar_hsa_circ_200349,RMVar_hsa_circ_3762,RMVar_hsa_circ_200359,RMVar_hsa_circ_374058,RMVar_hsa_circ_127517,RMVar_hsa_circ_200360,RMVar_hsa_circ_200371,RMVar_hsa_circ_106935,RMVar_hsa_circ_34337,RMVar_hsa_circ_200372,RMVar_hsa_circ_112999,RMVar_hsa_circ_76320,RMVar_hsa_circ_77703,RMVar_hsa_circ_200382,RMVar_hsa_circ_200383,RMVar_hsa_circ_104328,RMVar_hsa_circ_200388,RMVar_hsa_circ_40704,RMVar_hsa_circ_200389,RMVar_hsa_circ_78570,RMVar_hsa_circ_200395,RMVar_hsa_circ_67378,RMVar_hsa_circ_200399,RMVar_hsa_circ_120605,RMVar_hsa_circ_77721,RMVar_hsa_circ_200400,RMVar_hsa_circ_296828,RMVar_hsa_circ_60030,RMVar_hsa_circ_113678,RMVar_hsa_circ_200408,RMVar_hsa_circ_114391,RMVar_hsa_circ_200410,RMVar_hsa_circ_79531,RMVar_hsa_circ_200411,RMVar_hsa_circ_323520,RMVar_hsa_circ_200409,RMVar_hsa_circ_24659,RMVar_hsa_circ_200412,RMVar_hsa_circ_102056,RMVar_hsa_circ_125202,RMVar_hsa_circ_200419,RMVar_hsa_circ_200420,RMVar_hsa_circ_106370,RMVar_hsa_circ_200422,RMVar_hsa_circ_328280,RMVar_hsa_circ_351952,RMVar_hsa_circ_117262,RMVar_hsa_circ_200424,RMVar_hsa_circ_200431,RMVar_hsa_circ_370826,RMVar_hsa_circ_200423,RMVar_hsa_circ_319338,RMVar_hsa_circ_98377,RMVar_hsa_circ_62411,RMVar_hsa_circ_200434,RMVar_hsa_circ_200433,RMVar_hsa_circ_114277,RMVar_hsa_circ_116290,RMVar_hsa_circ_67986,RMVar_hsa_circ_200435,RMVar_hsa_circ_313314,RMVar_hsa_circ_97100,RMVar_hsa_circ_106675,RMVar_hsa_circ_2773,RMVar_hsa_circ_200437,RMVar_hsa_circ_200438,RMVar_hsa_circ_200436,RMVar_hsa_circ_352601,RMVar_hsa_circ_292017,RMVar_hsa_circ_267515,RMVar_hsa_circ_31336,RMVar_hsa_circ_8707,RMVar_hsa_circ_117913,RMVar_hsa_circ_200446,RMVar_hsa_circ_108413,RMVar_hsa_circ_268696,RMVar_hsa_circ_350272,RMVar_hsa_circ_200447,RMVar_hsa_circ_269731,RMVar_hsa_circ_200448,RMVar_hsa_circ_77627,RMVar_hsa_circ_2653,RMVar_hsa_circ_69736,RMVar_hsa_circ_200452,RMVar_hsa_circ_200454,RMVar_hsa_circ_8913,RMVar_hsa_circ_200462,RMVar_hsa_circ_32279,RMVar_hsa_circ_200457,RMVar_hsa_circ_283666,RMVar_hsa_circ_200456,RMVar_hsa_circ_291020,RMVar_hsa_circ_289548,RMVar_hsa_circ_24521,RMVar_hsa_circ_44631,RMVar_hsa_circ_200459,RMVar_hsa_circ_200458,RMVar_hsa_circ_74040,RMVar_hsa_circ_270121,RMVar_hsa_circ_358472,RMVar_hsa_circ_367224,RMVar_hsa_circ_102290,RMVar_hsa_circ_73133,RMVar_hsa_circ_7884,RMVar_hsa_circ_11256,RMVar_hsa_circ_200463,RMVar_hsa_circ_200464,RMVar_hsa_circ_200461,RMVar_hsa_circ_377081 45259 RMVar_ID_45259 Human_SNP_ID_74564551 A-to-I Human chr2 - 61336326 61336326 61336326 GCCCAGTAGTTTGAGACCAGCCTTGGAAACATAGGAAGACCCCATCTCTACAGAAAAACTTTAAA GCCCAGTAGTTTGAGACCAGCCTTGGAAACATCGGAAGACCCCATCTCTACAGAAAAACTTTAAA T G USP34 Ensembl:ENSG00000115464 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs755551236 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25554779 RMVar_hsa_circ_200292,RMVar_hsa_circ_102784,RMVar_hsa_circ_99836,RMVar_hsa_circ_200276,RMVar_hsa_circ_200277,RMVar_hsa_circ_114329,RMVar_hsa_circ_200282,RMVar_hsa_circ_96988,RMVar_hsa_circ_200283,RMVar_hsa_circ_124258,RMVar_hsa_circ_109206,RMVar_hsa_circ_200291,RMVar_hsa_circ_113788,RMVar_hsa_circ_109227,RMVar_hsa_circ_200304,RMVar_hsa_circ_200303,RMVar_hsa_circ_89816,RMVar_hsa_circ_200309,RMVar_hsa_circ_118352,RMVar_hsa_circ_14359,RMVar_hsa_circ_200327,RMVar_hsa_circ_119244,RMVar_hsa_circ_200333,RMVar_hsa_circ_96734,RMVar_hsa_circ_200334,RMVar_hsa_circ_98682,RMVar_hsa_circ_100601,RMVar_hsa_circ_92775,RMVar_hsa_circ_200347,RMVar_hsa_circ_200348,RMVar_hsa_circ_122046,RMVar_hsa_circ_200349,RMVar_hsa_circ_3762,RMVar_hsa_circ_200359,RMVar_hsa_circ_374058,RMVar_hsa_circ_127517,RMVar_hsa_circ_200360,RMVar_hsa_circ_200371,RMVar_hsa_circ_106935,RMVar_hsa_circ_34337,RMVar_hsa_circ_200372,RMVar_hsa_circ_112999,RMVar_hsa_circ_76320,RMVar_hsa_circ_77703,RMVar_hsa_circ_200382,RMVar_hsa_circ_200383,RMVar_hsa_circ_104328,RMVar_hsa_circ_200388,RMVar_hsa_circ_40704,RMVar_hsa_circ_200389,RMVar_hsa_circ_78570,RMVar_hsa_circ_200395,RMVar_hsa_circ_67378,RMVar_hsa_circ_200399,RMVar_hsa_circ_120605,RMVar_hsa_circ_77721,RMVar_hsa_circ_200400,RMVar_hsa_circ_296828,RMVar_hsa_circ_60030,RMVar_hsa_circ_113678,RMVar_hsa_circ_200408,RMVar_hsa_circ_114391,RMVar_hsa_circ_200410,RMVar_hsa_circ_79531,RMVar_hsa_circ_200411,RMVar_hsa_circ_323520,RMVar_hsa_circ_200409,RMVar_hsa_circ_24659,RMVar_hsa_circ_200412,RMVar_hsa_circ_102056,RMVar_hsa_circ_125202,RMVar_hsa_circ_200419,RMVar_hsa_circ_200420,RMVar_hsa_circ_106370,RMVar_hsa_circ_200422,RMVar_hsa_circ_328280,RMVar_hsa_circ_351952,RMVar_hsa_circ_117262,RMVar_hsa_circ_200424,RMVar_hsa_circ_200431,RMVar_hsa_circ_370826,RMVar_hsa_circ_200423,RMVar_hsa_circ_319338,RMVar_hsa_circ_98377,RMVar_hsa_circ_62411,RMVar_hsa_circ_200434,RMVar_hsa_circ_200433,RMVar_hsa_circ_114277,RMVar_hsa_circ_116290,RMVar_hsa_circ_67986,RMVar_hsa_circ_200435,RMVar_hsa_circ_313314,RMVar_hsa_circ_97100,RMVar_hsa_circ_106675,RMVar_hsa_circ_2773,RMVar_hsa_circ_200437,RMVar_hsa_circ_200438,RMVar_hsa_circ_200436,RMVar_hsa_circ_352601,RMVar_hsa_circ_292017,RMVar_hsa_circ_267515,RMVar_hsa_circ_31336,RMVar_hsa_circ_8707,RMVar_hsa_circ_117913,RMVar_hsa_circ_200446,RMVar_hsa_circ_108413,RMVar_hsa_circ_268696,RMVar_hsa_circ_350272,RMVar_hsa_circ_200447,RMVar_hsa_circ_269731,RMVar_hsa_circ_200448,RMVar_hsa_circ_77627,RMVar_hsa_circ_2653,RMVar_hsa_circ_69736,RMVar_hsa_circ_200452,RMVar_hsa_circ_200454,RMVar_hsa_circ_8913,RMVar_hsa_circ_200462,RMVar_hsa_circ_32279,RMVar_hsa_circ_200457,RMVar_hsa_circ_283666,RMVar_hsa_circ_200456,RMVar_hsa_circ_291020,RMVar_hsa_circ_289548,RMVar_hsa_circ_24521,RMVar_hsa_circ_44631,RMVar_hsa_circ_200459,RMVar_hsa_circ_200458,RMVar_hsa_circ_74040,RMVar_hsa_circ_270121,RMVar_hsa_circ_358472,RMVar_hsa_circ_367224,RMVar_hsa_circ_102290,RMVar_hsa_circ_73133,RMVar_hsa_circ_7884,RMVar_hsa_circ_11256,RMVar_hsa_circ_200463,RMVar_hsa_circ_200464,RMVar_hsa_circ_200461,RMVar_hsa_circ_377081 45260 RMVar_ID_45260 Human_SNP_ID_74565005 A-to-I Human chr2 - 61337583 61337583 61337583 AGATGTGGTGGTGTGTGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGTAGGAGGATTGCTTGTG AGATGTGGTGGTGTGTGCCTGTAGTCCCAGCTCCTTGGGAGGCTGAGGTAGGAGGATTGCTTGTG T G USP34 Ensembl:ENSG00000115464 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs964073495 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_200292,RMVar_hsa_circ_102784,RMVar_hsa_circ_99836,RMVar_hsa_circ_200276,RMVar_hsa_circ_200277,RMVar_hsa_circ_114329,RMVar_hsa_circ_200282,RMVar_hsa_circ_96988,RMVar_hsa_circ_200283,RMVar_hsa_circ_124258,RMVar_hsa_circ_109206,RMVar_hsa_circ_200291,RMVar_hsa_circ_113788,RMVar_hsa_circ_109227,RMVar_hsa_circ_200304,RMVar_hsa_circ_200303,RMVar_hsa_circ_89816,RMVar_hsa_circ_200309,RMVar_hsa_circ_118352,RMVar_hsa_circ_14359,RMVar_hsa_circ_200327,RMVar_hsa_circ_119244,RMVar_hsa_circ_200333,RMVar_hsa_circ_96734,RMVar_hsa_circ_200334,RMVar_hsa_circ_98682,RMVar_hsa_circ_100601,RMVar_hsa_circ_92775,RMVar_hsa_circ_200347,RMVar_hsa_circ_200348,RMVar_hsa_circ_122046,RMVar_hsa_circ_200349,RMVar_hsa_circ_3762,RMVar_hsa_circ_200359,RMVar_hsa_circ_374058,RMVar_hsa_circ_127517,RMVar_hsa_circ_200360,RMVar_hsa_circ_200371,RMVar_hsa_circ_106935,RMVar_hsa_circ_34337,RMVar_hsa_circ_200372,RMVar_hsa_circ_112999,RMVar_hsa_circ_76320,RMVar_hsa_circ_77703,RMVar_hsa_circ_200382,RMVar_hsa_circ_200383,RMVar_hsa_circ_104328,RMVar_hsa_circ_200388,RMVar_hsa_circ_40704,RMVar_hsa_circ_200389,RMVar_hsa_circ_78570,RMVar_hsa_circ_200395,RMVar_hsa_circ_67378,RMVar_hsa_circ_200399,RMVar_hsa_circ_120605,RMVar_hsa_circ_77721,RMVar_hsa_circ_200400,RMVar_hsa_circ_296828,RMVar_hsa_circ_60030,RMVar_hsa_circ_113678,RMVar_hsa_circ_200408,RMVar_hsa_circ_114391,RMVar_hsa_circ_200410,RMVar_hsa_circ_79531,RMVar_hsa_circ_200411,RMVar_hsa_circ_323520,RMVar_hsa_circ_200409,RMVar_hsa_circ_24659,RMVar_hsa_circ_200412,RMVar_hsa_circ_102056,RMVar_hsa_circ_125202,RMVar_hsa_circ_200419,RMVar_hsa_circ_200420,RMVar_hsa_circ_106370,RMVar_hsa_circ_200422,RMVar_hsa_circ_328280,RMVar_hsa_circ_351952,RMVar_hsa_circ_117262,RMVar_hsa_circ_200424,RMVar_hsa_circ_200431,RMVar_hsa_circ_370826,RMVar_hsa_circ_200423,RMVar_hsa_circ_319338,RMVar_hsa_circ_98377,RMVar_hsa_circ_62411,RMVar_hsa_circ_200434,RMVar_hsa_circ_200433,RMVar_hsa_circ_114277,RMVar_hsa_circ_116290,RMVar_hsa_circ_67986,RMVar_hsa_circ_200435,RMVar_hsa_circ_313314,RMVar_hsa_circ_97100,RMVar_hsa_circ_106675,RMVar_hsa_circ_2773,RMVar_hsa_circ_200437,RMVar_hsa_circ_200438,RMVar_hsa_circ_200436,RMVar_hsa_circ_352601,RMVar_hsa_circ_292017,RMVar_hsa_circ_267515,RMVar_hsa_circ_31336,RMVar_hsa_circ_8707,RMVar_hsa_circ_117913,RMVar_hsa_circ_200446,RMVar_hsa_circ_108413,RMVar_hsa_circ_268696,RMVar_hsa_circ_350272,RMVar_hsa_circ_200447,RMVar_hsa_circ_269731,RMVar_hsa_circ_200448,RMVar_hsa_circ_77627,RMVar_hsa_circ_2653,RMVar_hsa_circ_69736,RMVar_hsa_circ_200452,RMVar_hsa_circ_200454,RMVar_hsa_circ_8913,RMVar_hsa_circ_200462,RMVar_hsa_circ_32279,RMVar_hsa_circ_200457,RMVar_hsa_circ_283666,RMVar_hsa_circ_200456,RMVar_hsa_circ_291020,RMVar_hsa_circ_289548,RMVar_hsa_circ_24521,RMVar_hsa_circ_44631,RMVar_hsa_circ_200459,RMVar_hsa_circ_200458,RMVar_hsa_circ_74040,RMVar_hsa_circ_270121,RMVar_hsa_circ_358472,RMVar_hsa_circ_367224,RMVar_hsa_circ_102290,RMVar_hsa_circ_73133,RMVar_hsa_circ_7884,RMVar_hsa_circ_11256,RMVar_hsa_circ_200463,RMVar_hsa_circ_200464,RMVar_hsa_circ_200461,RMVar_hsa_circ_377081 45261 RMVar_ID_45261 Human_SNP_ID_74565025 A-to-I Human chr2 - 61337654 61337654 61337654 TCCAGGACTGAGACCAGCATGGGCAATGTGGTAAAACCTCGCCTCTACAAAAAATACAAATAAAA TCCAGGACTGAGACCAGCATGGGCAATGTGGTGAAACCTCGCCTCTACAAAAAATACAAATAAAA T C USP34 Ensembl:ENSG00000115464 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs949637176 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_200292,RMVar_hsa_circ_102784,RMVar_hsa_circ_99836,RMVar_hsa_circ_200276,RMVar_hsa_circ_200277,RMVar_hsa_circ_114329,RMVar_hsa_circ_200282,RMVar_hsa_circ_96988,RMVar_hsa_circ_200283,RMVar_hsa_circ_124258,RMVar_hsa_circ_109206,RMVar_hsa_circ_200291,RMVar_hsa_circ_113788,RMVar_hsa_circ_109227,RMVar_hsa_circ_200304,RMVar_hsa_circ_200303,RMVar_hsa_circ_89816,RMVar_hsa_circ_200309,RMVar_hsa_circ_118352,RMVar_hsa_circ_14359,RMVar_hsa_circ_200327,RMVar_hsa_circ_119244,RMVar_hsa_circ_200333,RMVar_hsa_circ_96734,RMVar_hsa_circ_200334,RMVar_hsa_circ_98682,RMVar_hsa_circ_100601,RMVar_hsa_circ_92775,RMVar_hsa_circ_200347,RMVar_hsa_circ_200348,RMVar_hsa_circ_122046,RMVar_hsa_circ_200349,RMVar_hsa_circ_3762,RMVar_hsa_circ_200359,RMVar_hsa_circ_374058,RMVar_hsa_circ_127517,RMVar_hsa_circ_200360,RMVar_hsa_circ_200371,RMVar_hsa_circ_106935,RMVar_hsa_circ_34337,RMVar_hsa_circ_200372,RMVar_hsa_circ_112999,RMVar_hsa_circ_76320,RMVar_hsa_circ_77703,RMVar_hsa_circ_200382,RMVar_hsa_circ_200383,RMVar_hsa_circ_104328,RMVar_hsa_circ_200388,RMVar_hsa_circ_40704,RMVar_hsa_circ_200389,RMVar_hsa_circ_78570,RMVar_hsa_circ_200395,RMVar_hsa_circ_67378,RMVar_hsa_circ_200399,RMVar_hsa_circ_120605,RMVar_hsa_circ_77721,RMVar_hsa_circ_200400,RMVar_hsa_circ_296828,RMVar_hsa_circ_60030,RMVar_hsa_circ_113678,RMVar_hsa_circ_200408,RMVar_hsa_circ_114391,RMVar_hsa_circ_200410,RMVar_hsa_circ_79531,RMVar_hsa_circ_200411,RMVar_hsa_circ_323520,RMVar_hsa_circ_200409,RMVar_hsa_circ_24659,RMVar_hsa_circ_200412,RMVar_hsa_circ_102056,RMVar_hsa_circ_125202,RMVar_hsa_circ_200419,RMVar_hsa_circ_200420,RMVar_hsa_circ_106370,RMVar_hsa_circ_200422,RMVar_hsa_circ_328280,RMVar_hsa_circ_351952,RMVar_hsa_circ_117262,RMVar_hsa_circ_200424,RMVar_hsa_circ_200431,RMVar_hsa_circ_370826,RMVar_hsa_circ_200423,RMVar_hsa_circ_319338,RMVar_hsa_circ_98377,RMVar_hsa_circ_62411,RMVar_hsa_circ_200434,RMVar_hsa_circ_200433,RMVar_hsa_circ_114277,RMVar_hsa_circ_116290,RMVar_hsa_circ_67986,RMVar_hsa_circ_200435,RMVar_hsa_circ_313314,RMVar_hsa_circ_97100,RMVar_hsa_circ_106675,RMVar_hsa_circ_2773,RMVar_hsa_circ_200437,RMVar_hsa_circ_200438,RMVar_hsa_circ_200436,RMVar_hsa_circ_352601,RMVar_hsa_circ_292017,RMVar_hsa_circ_267515,RMVar_hsa_circ_31336,RMVar_hsa_circ_8707,RMVar_hsa_circ_117913,RMVar_hsa_circ_200446,RMVar_hsa_circ_108413,RMVar_hsa_circ_268696,RMVar_hsa_circ_350272,RMVar_hsa_circ_200447,RMVar_hsa_circ_269731,RMVar_hsa_circ_200448,RMVar_hsa_circ_77627,RMVar_hsa_circ_2653,RMVar_hsa_circ_69736,RMVar_hsa_circ_200452,RMVar_hsa_circ_200454,RMVar_hsa_circ_8913,RMVar_hsa_circ_200462,RMVar_hsa_circ_32279,RMVar_hsa_circ_200457,RMVar_hsa_circ_283666,RMVar_hsa_circ_200456,RMVar_hsa_circ_291020,RMVar_hsa_circ_289548,RMVar_hsa_circ_24521,RMVar_hsa_circ_44631,RMVar_hsa_circ_200459,RMVar_hsa_circ_200458,RMVar_hsa_circ_74040,RMVar_hsa_circ_270121,RMVar_hsa_circ_358472,RMVar_hsa_circ_367224,RMVar_hsa_circ_102290,RMVar_hsa_circ_73133,RMVar_hsa_circ_7884,RMVar_hsa_circ_11256,RMVar_hsa_circ_200463,RMVar_hsa_circ_200464,RMVar_hsa_circ_200461,RMVar_hsa_circ_377081 45262 RMVar_ID_45262 Human_SNP_ID_74565186 A-to-I Human chr2 - 61338199 61338199 61338199 CTCCCACCTCAGCCTCCTGAGTAGCTGGGATTACAGGCACCTGCCATCATGGCTGGCTAATTTTT CTCCCACCTCAGCCTCCTGAGTAGCTGGGATTGCAGGCACCTGCCATCATGGCTGGCTAATTTTT T C USP34 Ensembl:ENSG00000115464 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs895972493 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_200292,RMVar_hsa_circ_102784,RMVar_hsa_circ_99836,RMVar_hsa_circ_200276,RMVar_hsa_circ_200277,RMVar_hsa_circ_114329,RMVar_hsa_circ_200282,RMVar_hsa_circ_96988,RMVar_hsa_circ_200283,RMVar_hsa_circ_124258,RMVar_hsa_circ_109206,RMVar_hsa_circ_200291,RMVar_hsa_circ_113788,RMVar_hsa_circ_109227,RMVar_hsa_circ_200304,RMVar_hsa_circ_200303,RMVar_hsa_circ_89816,RMVar_hsa_circ_200309,RMVar_hsa_circ_118352,RMVar_hsa_circ_14359,RMVar_hsa_circ_200327,RMVar_hsa_circ_119244,RMVar_hsa_circ_200333,RMVar_hsa_circ_96734,RMVar_hsa_circ_200334,RMVar_hsa_circ_98682,RMVar_hsa_circ_100601,RMVar_hsa_circ_92775,RMVar_hsa_circ_200347,RMVar_hsa_circ_200348,RMVar_hsa_circ_122046,RMVar_hsa_circ_200349,RMVar_hsa_circ_3762,RMVar_hsa_circ_200359,RMVar_hsa_circ_374058,RMVar_hsa_circ_127517,RMVar_hsa_circ_200360,RMVar_hsa_circ_200371,RMVar_hsa_circ_106935,RMVar_hsa_circ_34337,RMVar_hsa_circ_200372,RMVar_hsa_circ_112999,RMVar_hsa_circ_76320,RMVar_hsa_circ_77703,RMVar_hsa_circ_200382,RMVar_hsa_circ_200383,RMVar_hsa_circ_104328,RMVar_hsa_circ_200388,RMVar_hsa_circ_40704,RMVar_hsa_circ_200389,RMVar_hsa_circ_78570,RMVar_hsa_circ_200395,RMVar_hsa_circ_67378,RMVar_hsa_circ_200399,RMVar_hsa_circ_120605,RMVar_hsa_circ_77721,RMVar_hsa_circ_200400,RMVar_hsa_circ_296828,RMVar_hsa_circ_60030,RMVar_hsa_circ_113678,RMVar_hsa_circ_200408,RMVar_hsa_circ_114391,RMVar_hsa_circ_200410,RMVar_hsa_circ_79531,RMVar_hsa_circ_200411,RMVar_hsa_circ_323520,RMVar_hsa_circ_200409,RMVar_hsa_circ_24659,RMVar_hsa_circ_200412,RMVar_hsa_circ_102056,RMVar_hsa_circ_125202,RMVar_hsa_circ_200419,RMVar_hsa_circ_200420,RMVar_hsa_circ_106370,RMVar_hsa_circ_200422,RMVar_hsa_circ_328280,RMVar_hsa_circ_351952,RMVar_hsa_circ_117262,RMVar_hsa_circ_200424,RMVar_hsa_circ_200431,RMVar_hsa_circ_370826,RMVar_hsa_circ_200423,RMVar_hsa_circ_319338,RMVar_hsa_circ_98377,RMVar_hsa_circ_62411,RMVar_hsa_circ_200434,RMVar_hsa_circ_200433,RMVar_hsa_circ_114277,RMVar_hsa_circ_116290,RMVar_hsa_circ_67986,RMVar_hsa_circ_200435,RMVar_hsa_circ_313314,RMVar_hsa_circ_97100,RMVar_hsa_circ_106675,RMVar_hsa_circ_2773,RMVar_hsa_circ_200437,RMVar_hsa_circ_200438,RMVar_hsa_circ_200436,RMVar_hsa_circ_352601,RMVar_hsa_circ_292017,RMVar_hsa_circ_267515,RMVar_hsa_circ_31336,RMVar_hsa_circ_8707,RMVar_hsa_circ_117913,RMVar_hsa_circ_200446,RMVar_hsa_circ_108413,RMVar_hsa_circ_268696,RMVar_hsa_circ_350272,RMVar_hsa_circ_200447,RMVar_hsa_circ_269731,RMVar_hsa_circ_200448,RMVar_hsa_circ_77627,RMVar_hsa_circ_2653,RMVar_hsa_circ_69736,RMVar_hsa_circ_200452,RMVar_hsa_circ_200454,RMVar_hsa_circ_8913,RMVar_hsa_circ_200462,RMVar_hsa_circ_32279,RMVar_hsa_circ_200457,RMVar_hsa_circ_283666,RMVar_hsa_circ_200456,RMVar_hsa_circ_291020,RMVar_hsa_circ_289548,RMVar_hsa_circ_24521,RMVar_hsa_circ_44631,RMVar_hsa_circ_200459,RMVar_hsa_circ_200458,RMVar_hsa_circ_74040,RMVar_hsa_circ_270121,RMVar_hsa_circ_358472,RMVar_hsa_circ_367224,RMVar_hsa_circ_102290,RMVar_hsa_circ_73133,RMVar_hsa_circ_7884,RMVar_hsa_circ_11256,RMVar_hsa_circ_200463,RMVar_hsa_circ_200464,RMVar_hsa_circ_200461,RMVar_hsa_circ_377081 45263 RMVar_ID_45263 Human_SNP_ID_74567732 A-to-I Human chr2 - 61345689 61345689 61345689 TCAAGACTGCAGTGAGTGGTGATTGCACCACTACACTTCAGCCTGGGCAATAGAATGAGACTCTG TCAAGACTGCAGTGAGTGGTGATTGCACCACTGCACTTCAGCCTGGGCAATAGAATGAGACTCTG T C USP34 Ensembl:ENSG00000115464 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs191544638 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13928397 RMVar_hsa_circ_200292,RMVar_hsa_circ_102784,RMVar_hsa_circ_99836,RMVar_hsa_circ_200276,RMVar_hsa_circ_200277,RMVar_hsa_circ_114329,RMVar_hsa_circ_200282,RMVar_hsa_circ_96988,RMVar_hsa_circ_200283,RMVar_hsa_circ_124258,RMVar_hsa_circ_109206,RMVar_hsa_circ_200291,RMVar_hsa_circ_113788,RMVar_hsa_circ_109227,RMVar_hsa_circ_200304,RMVar_hsa_circ_200303,RMVar_hsa_circ_89816,RMVar_hsa_circ_200309,RMVar_hsa_circ_118352,RMVar_hsa_circ_14359,RMVar_hsa_circ_200327,RMVar_hsa_circ_119244,RMVar_hsa_circ_200333,RMVar_hsa_circ_96734,RMVar_hsa_circ_200334,RMVar_hsa_circ_98682,RMVar_hsa_circ_100601,RMVar_hsa_circ_92775,RMVar_hsa_circ_200347,RMVar_hsa_circ_200348,RMVar_hsa_circ_122046,RMVar_hsa_circ_200349,RMVar_hsa_circ_3762,RMVar_hsa_circ_200359,RMVar_hsa_circ_374058,RMVar_hsa_circ_127517,RMVar_hsa_circ_200360,RMVar_hsa_circ_200371,RMVar_hsa_circ_112999,RMVar_hsa_circ_76320,RMVar_hsa_circ_77703,RMVar_hsa_circ_200382,RMVar_hsa_circ_200383,RMVar_hsa_circ_104328,RMVar_hsa_circ_200388,RMVar_hsa_circ_40704,RMVar_hsa_circ_200389,RMVar_hsa_circ_78570,RMVar_hsa_circ_200395,RMVar_hsa_circ_67378,RMVar_hsa_circ_200399,RMVar_hsa_circ_120605,RMVar_hsa_circ_77721,RMVar_hsa_circ_200400,RMVar_hsa_circ_296828,RMVar_hsa_circ_113678,RMVar_hsa_circ_200408,RMVar_hsa_circ_114391,RMVar_hsa_circ_200410,RMVar_hsa_circ_79531,RMVar_hsa_circ_200411,RMVar_hsa_circ_323520,RMVar_hsa_circ_200409,RMVar_hsa_circ_24659,RMVar_hsa_circ_200412,RMVar_hsa_circ_102056,RMVar_hsa_circ_125202,RMVar_hsa_circ_200419,RMVar_hsa_circ_200420,RMVar_hsa_circ_106370,RMVar_hsa_circ_200422,RMVar_hsa_circ_328280,RMVar_hsa_circ_351952,RMVar_hsa_circ_200431,RMVar_hsa_circ_370826,RMVar_hsa_circ_200423,RMVar_hsa_circ_319338,RMVar_hsa_circ_98377,RMVar_hsa_circ_200434,RMVar_hsa_circ_200433,RMVar_hsa_circ_114277,RMVar_hsa_circ_116290,RMVar_hsa_circ_67986,RMVar_hsa_circ_200435,RMVar_hsa_circ_97100,RMVar_hsa_circ_106675,RMVar_hsa_circ_200437,RMVar_hsa_circ_200436,RMVar_hsa_circ_352601,RMVar_hsa_circ_292017,RMVar_hsa_circ_267515,RMVar_hsa_circ_31336,RMVar_hsa_circ_8707,RMVar_hsa_circ_117913,RMVar_hsa_circ_200446,RMVar_hsa_circ_108413,RMVar_hsa_circ_268696,RMVar_hsa_circ_350272,RMVar_hsa_circ_200447,RMVar_hsa_circ_269731,RMVar_hsa_circ_200448,RMVar_hsa_circ_77627,RMVar_hsa_circ_200452,RMVar_hsa_circ_200454,RMVar_hsa_circ_8913,RMVar_hsa_circ_200462,RMVar_hsa_circ_32279,RMVar_hsa_circ_200457,RMVar_hsa_circ_283666,RMVar_hsa_circ_200456,RMVar_hsa_circ_24521,RMVar_hsa_circ_44631,RMVar_hsa_circ_74040,RMVar_hsa_circ_270121,RMVar_hsa_circ_358472,RMVar_hsa_circ_73133,RMVar_hsa_circ_11256,RMVar_hsa_circ_200463,RMVar_hsa_circ_200466,RMVar_hsa_circ_200464,RMVar_hsa_circ_377081,RMVar_hsa_circ_277555,RMVar_hsa_circ_371996,RMVar_hsa_circ_200467,RMVar_hsa_circ_85712,RMVar_hsa_circ_277047,RMVar_hsa_circ_371606,RMVar_hsa_circ_200468,RMVar_hsa_circ_296479,RMVar_hsa_circ_78659,RMVar_hsa_circ_200469,RMVar_hsa_circ_200471,RMVar_hsa_circ_200470 45264 RMVar_ID_45264 Human_SNP_ID_74574751 A-to-I Human chr2 - 61366927 61366927 61366927 GTCCCACCTCAGCCTCCTAAGTAGCTGGGACTACAGATGCACACCACCATGCTTGGCTAATTTTT GTCCCACCTCAGCCTCCTAAGTAGCTGGGACTGCAGATGCACACCACCATGCTTGGCTAATTTTT T C USP34 Ensembl:ENSG00000115464 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs914439504 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99836,RMVar_hsa_circ_200277,RMVar_hsa_circ_124258,RMVar_hsa_circ_200291,RMVar_hsa_circ_113788,RMVar_hsa_circ_200303,RMVar_hsa_circ_118352,RMVar_hsa_circ_200327,RMVar_hsa_circ_100601,RMVar_hsa_circ_92775,RMVar_hsa_circ_200348,RMVar_hsa_circ_3762,RMVar_hsa_circ_200359,RMVar_hsa_circ_76320,RMVar_hsa_circ_77703,RMVar_hsa_circ_200383,RMVar_hsa_circ_40704,RMVar_hsa_circ_200389,RMVar_hsa_circ_67378,RMVar_hsa_circ_114391,RMVar_hsa_circ_200410,RMVar_hsa_circ_79531,RMVar_hsa_circ_200411,RMVar_hsa_circ_24659,RMVar_hsa_circ_106370,RMVar_hsa_circ_200422,RMVar_hsa_circ_351952,RMVar_hsa_circ_200434,RMVar_hsa_circ_114277,RMVar_hsa_circ_116290,RMVar_hsa_circ_67986,RMVar_hsa_circ_200435,RMVar_hsa_circ_352601,RMVar_hsa_circ_267515,RMVar_hsa_circ_31336,RMVar_hsa_circ_8707,RMVar_hsa_circ_117913,RMVar_hsa_circ_108413,RMVar_hsa_circ_268696,RMVar_hsa_circ_200447,RMVar_hsa_circ_200448,RMVar_hsa_circ_32279,RMVar_hsa_circ_200456,RMVar_hsa_circ_24521,RMVar_hsa_circ_44631,RMVar_hsa_circ_74040,RMVar_hsa_circ_358472,RMVar_hsa_circ_11256,RMVar_hsa_circ_200463,RMVar_hsa_circ_79510,RMVar_hsa_circ_371996,RMVar_hsa_circ_200467,RMVar_hsa_circ_296479,RMVar_hsa_circ_78659,RMVar_hsa_circ_200469,RMVar_hsa_circ_200476,RMVar_hsa_circ_120002,RMVar_hsa_circ_200478,RMVar_hsa_circ_113108,RMVar_hsa_circ_200479,RMVar_hsa_circ_200481,RMVar_hsa_circ_36581,RMVar_hsa_circ_72054,RMVar_hsa_circ_265331,RMVar_hsa_circ_37198 45265 RMVar_ID_45265 Human_SNP_ID_74576635 A-to-I Human chr2 - 61372648 61372648 61372648 GGAGTGCAGCAACAGCACGATTATGCCTTACTACAGCTCTGACCTGGACTCAAATGATCCTCCCA GGAGTGCAGCAACAGCACGATTATGCCTTACTGCAGCTCTGACCTGGACTCAAATGATCCTCCCA T C USP34 Ensembl:ENSG00000115464 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs972241303 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13928952,Human_RBP_ID_18763232,Human_RBP_ID_23878640 RMVar_hsa_circ_124258,RMVar_hsa_circ_200291,RMVar_hsa_circ_113788,RMVar_hsa_circ_200303,RMVar_hsa_circ_100601,RMVar_hsa_circ_200348,RMVar_hsa_circ_3762,RMVar_hsa_circ_40704,RMVar_hsa_circ_67378,RMVar_hsa_circ_114391,RMVar_hsa_circ_200410,RMVar_hsa_circ_79531,RMVar_hsa_circ_200411,RMVar_hsa_circ_24659,RMVar_hsa_circ_106370,RMVar_hsa_circ_200422,RMVar_hsa_circ_351952,RMVar_hsa_circ_116290,RMVar_hsa_circ_200435,RMVar_hsa_circ_31336,RMVar_hsa_circ_8707,RMVar_hsa_circ_108413,RMVar_hsa_circ_200447,RMVar_hsa_circ_32279,RMVar_hsa_circ_24521,RMVar_hsa_circ_74040,RMVar_hsa_circ_358472,RMVar_hsa_circ_200463,RMVar_hsa_circ_79510,RMVar_hsa_circ_371996,RMVar_hsa_circ_200467,RMVar_hsa_circ_296479,RMVar_hsa_circ_78659,RMVar_hsa_circ_200469,RMVar_hsa_circ_200476,RMVar_hsa_circ_120002,RMVar_hsa_circ_200478,RMVar_hsa_circ_113108,RMVar_hsa_circ_200479,RMVar_hsa_circ_200486,RMVar_hsa_circ_111072,RMVar_hsa_circ_200481,RMVar_hsa_circ_36581,RMVar_hsa_circ_72054,RMVar_hsa_circ_37198,RMVar_hsa_circ_296043,RMVar_hsa_circ_322757,RMVar_hsa_circ_303740,RMVar_hsa_circ_279638,RMVar_hsa_circ_290347,RMVar_hsa_circ_200488,RMVar_hsa_circ_43597,RMVar_hsa_circ_200489,RMVar_hsa_circ_200487,RMVar_hsa_circ_200484,RMVar_hsa_circ_200485 45266 RMVar_ID_45266 Human_SNP_ID_74577362 A-to-I Human chr2 - 61374712 61374712 61374712 ATACAAAAATTAGCTGGGCCTGGTGGTGAATCACTTGAACCTGAGAGGTGGAGTTTGCAGTGAGC ATACAAAAATTAGCTGGGCCTGGTGGTGAATCGCTTGAACCTGAGAGGTGGAGTTTGCAGTGAGC T C USP34 Ensembl:ENSG00000115464 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1267326547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25555170 RMVar_hsa_circ_124258,RMVar_hsa_circ_200291,RMVar_hsa_circ_113788,RMVar_hsa_circ_200303,RMVar_hsa_circ_100601,RMVar_hsa_circ_200348,RMVar_hsa_circ_3762,RMVar_hsa_circ_40704,RMVar_hsa_circ_67378,RMVar_hsa_circ_114391,RMVar_hsa_circ_200410,RMVar_hsa_circ_79531,RMVar_hsa_circ_200411,RMVar_hsa_circ_24659,RMVar_hsa_circ_106370,RMVar_hsa_circ_200422,RMVar_hsa_circ_351952,RMVar_hsa_circ_116290,RMVar_hsa_circ_200435,RMVar_hsa_circ_31336,RMVar_hsa_circ_8707,RMVar_hsa_circ_108413,RMVar_hsa_circ_200447,RMVar_hsa_circ_32279,RMVar_hsa_circ_24521,RMVar_hsa_circ_74040,RMVar_hsa_circ_358472,RMVar_hsa_circ_200463,RMVar_hsa_circ_79510,RMVar_hsa_circ_371996,RMVar_hsa_circ_200467,RMVar_hsa_circ_296479,RMVar_hsa_circ_78659,RMVar_hsa_circ_200469,RMVar_hsa_circ_200476,RMVar_hsa_circ_120002,RMVar_hsa_circ_200478,RMVar_hsa_circ_113108,RMVar_hsa_circ_200479,RMVar_hsa_circ_200486,RMVar_hsa_circ_111072,RMVar_hsa_circ_200481,RMVar_hsa_circ_36581,RMVar_hsa_circ_72054,RMVar_hsa_circ_37198,RMVar_hsa_circ_296043,RMVar_hsa_circ_322757,RMVar_hsa_circ_303740,RMVar_hsa_circ_279638,RMVar_hsa_circ_290347,RMVar_hsa_circ_200488,RMVar_hsa_circ_43597,RMVar_hsa_circ_200489,RMVar_hsa_circ_200487,RMVar_hsa_circ_200484,RMVar_hsa_circ_200485 45267 RMVar_ID_45267 Human_SNP_ID_74578412 A-to-I Human chr2 - 61377922 61377922 61377922 CACTTGCCTCAGTCTCCCAAAGTGTTGGGATTACAGGCGTGAGCCACTGTGTCTGGCCACATTTC CACTTGCCTCAGTCTCCCAAAGTGTTGGGATTGCAGGCGTGAGCCACTGTGTCTGGCCACATTTC T C USP34 Ensembl:ENSG00000115464 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1312715118 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25590487 RMVar_hsa_circ_124258,RMVar_hsa_circ_200291,RMVar_hsa_circ_113788,RMVar_hsa_circ_200303,RMVar_hsa_circ_100601,RMVar_hsa_circ_200348,RMVar_hsa_circ_3762,RMVar_hsa_circ_40704,RMVar_hsa_circ_67378,RMVar_hsa_circ_114391,RMVar_hsa_circ_200410,RMVar_hsa_circ_79531,RMVar_hsa_circ_200411,RMVar_hsa_circ_24659,RMVar_hsa_circ_106370,RMVar_hsa_circ_200422,RMVar_hsa_circ_351952,RMVar_hsa_circ_116290,RMVar_hsa_circ_200435,RMVar_hsa_circ_31336,RMVar_hsa_circ_8707,RMVar_hsa_circ_108413,RMVar_hsa_circ_200447,RMVar_hsa_circ_32279,RMVar_hsa_circ_24521,RMVar_hsa_circ_74040,RMVar_hsa_circ_358472,RMVar_hsa_circ_200463,RMVar_hsa_circ_79510,RMVar_hsa_circ_371996,RMVar_hsa_circ_200467,RMVar_hsa_circ_296479,RMVar_hsa_circ_78659,RMVar_hsa_circ_200469,RMVar_hsa_circ_200476,RMVar_hsa_circ_120002,RMVar_hsa_circ_200478,RMVar_hsa_circ_113108,RMVar_hsa_circ_200479,RMVar_hsa_circ_200486,RMVar_hsa_circ_111072,RMVar_hsa_circ_200481,RMVar_hsa_circ_36581,RMVar_hsa_circ_72054,RMVar_hsa_circ_37198,RMVar_hsa_circ_296043,RMVar_hsa_circ_322757,RMVar_hsa_circ_303740,RMVar_hsa_circ_279638,RMVar_hsa_circ_290347,RMVar_hsa_circ_200488,RMVar_hsa_circ_43597,RMVar_hsa_circ_200489,RMVar_hsa_circ_200487,RMVar_hsa_circ_200484,RMVar_hsa_circ_200485 45268 RMVar_ID_45268 Human_SNP_ID_74585056 A-to-I Human chr2 - 61396551 61396551 61396551 CCAGGAGGCAGAGCTTGCAGTGATCCGAGATCATGCTCCTGCACTCCAGCCTGAGCGACAGTGCG CCAGGAGGCAGAGCTTGCAGTGATCCGAGATCGTGCTCCTGCACTCCAGCCTGAGCGACAGTGCG T C USP34 Ensembl:ENSG00000115464 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432351464 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9992025,Human_RBP_ID_25590498 RMVar_hsa_circ_3762,RMVar_hsa_circ_40704,RMVar_hsa_circ_24659,RMVar_hsa_circ_31336,RMVar_hsa_circ_108413,RMVar_hsa_circ_200447,RMVar_hsa_circ_74040,RMVar_hsa_circ_371996,RMVar_hsa_circ_200467,RMVar_hsa_circ_78659,RMVar_hsa_circ_200469,RMVar_hsa_circ_113108,RMVar_hsa_circ_200479,RMVar_hsa_circ_322757,RMVar_hsa_circ_279638,RMVar_hsa_circ_200488,RMVar_hsa_circ_200489,RMVar_hsa_circ_326945,RMVar_hsa_circ_200491,RMVar_hsa_circ_200490,RMVar_hsa_circ_313215,RMVar_hsa_circ_358852 45269 RMVar_ID_45269 Human_SNP_ID_74585337 A-to-I Human chr2 - 61397360 61397360 61397360 TGACTCACTGCGACCTCCACCTCCTGGGTTCAAGCAGTTCTCCTGCATCAGCCTCCCAAGTAGCT TGACTCACTGCGACCTCCACCTCCTGGGTTCAGGCAGTTCTCCTGCATCAGCCTCCCAAGTAGCT T C USP34 Ensembl:ENSG00000115464 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1449135215 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3762,RMVar_hsa_circ_40704,RMVar_hsa_circ_24659,RMVar_hsa_circ_31336,RMVar_hsa_circ_108413,RMVar_hsa_circ_200447,RMVar_hsa_circ_74040,RMVar_hsa_circ_371996,RMVar_hsa_circ_200467,RMVar_hsa_circ_78659,RMVar_hsa_circ_200469,RMVar_hsa_circ_113108,RMVar_hsa_circ_200479,RMVar_hsa_circ_322757,RMVar_hsa_circ_279638,RMVar_hsa_circ_200488,RMVar_hsa_circ_200489,RMVar_hsa_circ_326945,RMVar_hsa_circ_200491,RMVar_hsa_circ_200490,RMVar_hsa_circ_313215,RMVar_hsa_circ_358852 45270 RMVar_ID_45270 Human_SNP_ID_74585531 A-to-I Human chr2 - 61397945 61397945 61397945 CTTGTGCCTTAGTCTGCTGAGCAGCTGGGATTACAGGCGTGTGCCATCACCCCTGGTTAATTTCT CTTGTGCCTTAGTCTGCTGAGCAGCTGGGATTCCAGGCGTGTGCCATCACCCCTGGTTAATTTCT T G USP34 Ensembl:ENSG00000115464 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1448190345 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3762,RMVar_hsa_circ_40704,RMVar_hsa_circ_24659,RMVar_hsa_circ_31336,RMVar_hsa_circ_108413,RMVar_hsa_circ_200447,RMVar_hsa_circ_74040,RMVar_hsa_circ_371996,RMVar_hsa_circ_200467,RMVar_hsa_circ_78659,RMVar_hsa_circ_200469,RMVar_hsa_circ_113108,RMVar_hsa_circ_200479,RMVar_hsa_circ_322757,RMVar_hsa_circ_279638,RMVar_hsa_circ_200488,RMVar_hsa_circ_200489,RMVar_hsa_circ_326945,RMVar_hsa_circ_200491,RMVar_hsa_circ_200490,RMVar_hsa_circ_313215,RMVar_hsa_circ_358852 45271 RMVar_ID_45271 Human_SNP_ID_74585573 A-to-I Human chr2 - 61398040 61398040 61398040 TGGAGGCGGAGTCTCGCTCTGTTGCCCAAGCTAGAGTGCATTGGTACAATCTTGACTCACTGCAA TGGAGGCGGAGTCTCGCTCTGTTGCCCAAGCTTGAGTGCATTGGTACAATCTTGACTCACTGCAA T A USP34 Ensembl:ENSG00000115464 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs975270579 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_242491,Human_RBP_ID_775214,Human_RBP_ID_3640812,Human_RBP_ID_13929551,Human_RBP_ID_17570736,Human_RBP_ID_18949197 RMVar_hsa_circ_3762,RMVar_hsa_circ_40704,RMVar_hsa_circ_24659,RMVar_hsa_circ_31336,RMVar_hsa_circ_108413,RMVar_hsa_circ_200447,RMVar_hsa_circ_74040,RMVar_hsa_circ_371996,RMVar_hsa_circ_200467,RMVar_hsa_circ_78659,RMVar_hsa_circ_200469,RMVar_hsa_circ_113108,RMVar_hsa_circ_200479,RMVar_hsa_circ_322757,RMVar_hsa_circ_279638,RMVar_hsa_circ_200488,RMVar_hsa_circ_200489,RMVar_hsa_circ_326945,RMVar_hsa_circ_200491,RMVar_hsa_circ_200490,RMVar_hsa_circ_313215,RMVar_hsa_circ_358852 45272 RMVar_ID_45272 Human_SNP_ID_74585657 A-to-I Human chr2 - 61398245 61398245 61398245 CTCCCGCCTCAGCCTCCTGAGTATCTGGGACAACAGACACGCACCACCATGCCTGGCTAATTTTT CTCCCGCCTCAGCCTCCTGAGTATCTGGGACAGCAGACACGCACCACCATGCCTGGCTAATTTTT T C USP34 Ensembl:ENSG00000115464 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1398451622 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13929558 RMVar_hsa_circ_3762,RMVar_hsa_circ_40704,RMVar_hsa_circ_24659,RMVar_hsa_circ_31336,RMVar_hsa_circ_108413,RMVar_hsa_circ_200447,RMVar_hsa_circ_74040,RMVar_hsa_circ_371996,RMVar_hsa_circ_200467,RMVar_hsa_circ_78659,RMVar_hsa_circ_200469,RMVar_hsa_circ_113108,RMVar_hsa_circ_200479,RMVar_hsa_circ_322757,RMVar_hsa_circ_279638,RMVar_hsa_circ_200488,RMVar_hsa_circ_200489,RMVar_hsa_circ_326945,RMVar_hsa_circ_200491,RMVar_hsa_circ_200490,RMVar_hsa_circ_313215,RMVar_hsa_circ_358852 45273 RMVar_ID_45273 Human_SNP_ID_74585669 A-to-I Human chr2 - 61398280 61398280 61398280 TCATTGCAGCCTAGACCTCCCAAGTTCATGCAATCCTCCCGCCTCAGCCTCCTGAGTATCTGGGA TCATTGCAGCCTAGACCTCCCAAGTTCATGCAGTCCTCCCGCCTCAGCCTCCTGAGTATCTGGGA T C USP34 Ensembl:ENSG00000115464 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs573904342 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3762,RMVar_hsa_circ_40704,RMVar_hsa_circ_24659,RMVar_hsa_circ_31336,RMVar_hsa_circ_108413,RMVar_hsa_circ_200447,RMVar_hsa_circ_74040,RMVar_hsa_circ_371996,RMVar_hsa_circ_200467,RMVar_hsa_circ_78659,RMVar_hsa_circ_200469,RMVar_hsa_circ_113108,RMVar_hsa_circ_200479,RMVar_hsa_circ_322757,RMVar_hsa_circ_279638,RMVar_hsa_circ_200488,RMVar_hsa_circ_200489,RMVar_hsa_circ_326945,RMVar_hsa_circ_200491,RMVar_hsa_circ_200490,RMVar_hsa_circ_313215,RMVar_hsa_circ_358852 45274 RMVar_ID_45274 Human_SNP_ID_74586498 A-to-I Human chr2 - 61400388 61400388 61400388 TGCCTTTCCTCTGGCCGGGCGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGC TGCCTTTCCTCTGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGC T C USP34 Ensembl:ENSG00000115464 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs940178933 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3762,RMVar_hsa_circ_40704,RMVar_hsa_circ_24659,RMVar_hsa_circ_31336,RMVar_hsa_circ_108413,RMVar_hsa_circ_200447,RMVar_hsa_circ_74040,RMVar_hsa_circ_371996,RMVar_hsa_circ_200467,RMVar_hsa_circ_78659,RMVar_hsa_circ_200469,RMVar_hsa_circ_113108,RMVar_hsa_circ_200479,RMVar_hsa_circ_322757,RMVar_hsa_circ_279638,RMVar_hsa_circ_200488,RMVar_hsa_circ_200489,RMVar_hsa_circ_326945,RMVar_hsa_circ_200490,RMVar_hsa_circ_313215,RMVar_hsa_circ_358852 45275 RMVar_ID_45275 Human_SNP_ID_74586687 A-to-I Human chr2 - 61400967 61400967 61400967 TTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGATGGTCTCAATCACTTGATCT TTTTGTATTTTTAGTAGAGACAGGGTTTCACCGTGTTGGCCAGGATGGTCTCAATCACTTGATCT T C USP34 Ensembl:ENSG00000115464 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1558572868 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3762,RMVar_hsa_circ_40704,RMVar_hsa_circ_24659,RMVar_hsa_circ_31336,RMVar_hsa_circ_108413,RMVar_hsa_circ_200447,RMVar_hsa_circ_74040,RMVar_hsa_circ_371996,RMVar_hsa_circ_200467,RMVar_hsa_circ_78659,RMVar_hsa_circ_200469,RMVar_hsa_circ_113108,RMVar_hsa_circ_200479,RMVar_hsa_circ_322757,RMVar_hsa_circ_279638,RMVar_hsa_circ_200488,RMVar_hsa_circ_200489,RMVar_hsa_circ_326945,RMVar_hsa_circ_200490,RMVar_hsa_circ_313215,RMVar_hsa_circ_358852 45276 RMVar_ID_45276 Human_SNP_ID_74586709 A-to-I Human chr2 - 61401064 61401064 61401064 TCACTGCAACCTCTGCCTCCTGGGTTCAGGCGATTCTCCTGCCTTAGCCTCCCAAGTAGCTGGGA TCACTGCAACCTCTGCCTCCTGGGTTCAGGCGCTTCTCCTGCCTTAGCCTCCCAAGTAGCTGGGA T G USP34 Ensembl:ENSG00000115464 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs760332770 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3762,RMVar_hsa_circ_40704,RMVar_hsa_circ_24659,RMVar_hsa_circ_31336,RMVar_hsa_circ_108413,RMVar_hsa_circ_200447,RMVar_hsa_circ_74040,RMVar_hsa_circ_371996,RMVar_hsa_circ_200467,RMVar_hsa_circ_78659,RMVar_hsa_circ_200469,RMVar_hsa_circ_113108,RMVar_hsa_circ_200479,RMVar_hsa_circ_322757,RMVar_hsa_circ_279638,RMVar_hsa_circ_200488,RMVar_hsa_circ_200489,RMVar_hsa_circ_326945,RMVar_hsa_circ_200490,RMVar_hsa_circ_313215,RMVar_hsa_circ_358852 45277 RMVar_ID_45277 Human_SNP_ID_74586872 A-to-I Human chr2 - 61401437 61401437 61401437 GGCCAGGAGTTTAAGTCTAGGCTGGGCAACATAGCAAGAGCTCATCTTTACAAAAGAAAAAAAAA GGCCAGGAGTTTAAGTCTAGGCTGGGCAACATGGCAAGAGCTCATCTTTACAAAAGAAAAAAAAA T C USP34 Ensembl:ENSG00000115464 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1186583076 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13929658 RMVar_hsa_circ_3762,RMVar_hsa_circ_40704,RMVar_hsa_circ_24659,RMVar_hsa_circ_31336,RMVar_hsa_circ_108413,RMVar_hsa_circ_200447,RMVar_hsa_circ_74040,RMVar_hsa_circ_371996,RMVar_hsa_circ_200467,RMVar_hsa_circ_78659,RMVar_hsa_circ_200469,RMVar_hsa_circ_113108,RMVar_hsa_circ_200479,RMVar_hsa_circ_322757,RMVar_hsa_circ_279638,RMVar_hsa_circ_200488,RMVar_hsa_circ_200489,RMVar_hsa_circ_326945,RMVar_hsa_circ_200490,RMVar_hsa_circ_313215,RMVar_hsa_circ_358852 45278 RMVar_ID_45278 Human_SNP_ID_74587026 A-to-I Human chr2 - 61401793 61401793 61401793 AGCACTTTTGGAGGCTGAGGCAGGTGGATCACAAGGTCAGGATATCGAGACCATCCTGGCTAACA AGCACTTTTGGAGGCTGAGGCAGGTGGATCACGAGGTCAGGATATCGAGACCATCCTGGCTAACA T C USP34 Ensembl:ENSG00000115464 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1418810756 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3762,RMVar_hsa_circ_40704,RMVar_hsa_circ_24659,RMVar_hsa_circ_31336,RMVar_hsa_circ_108413,RMVar_hsa_circ_200447,RMVar_hsa_circ_74040,RMVar_hsa_circ_371996,RMVar_hsa_circ_200467,RMVar_hsa_circ_78659,RMVar_hsa_circ_200469,RMVar_hsa_circ_113108,RMVar_hsa_circ_200479,RMVar_hsa_circ_322757,RMVar_hsa_circ_279638,RMVar_hsa_circ_200488,RMVar_hsa_circ_200489,RMVar_hsa_circ_326945,RMVar_hsa_circ_200490,RMVar_hsa_circ_313215,RMVar_hsa_circ_358852 45279 RMVar_ID_45279 Human_SNP_ID_74604860 A-to-I Human chr2 - 61454405 61454405 61454405 ACAAACAAAAAACTGGCTGGGCGCAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAG ACAAACAAAAAACTGGCTGGGCGCAGTGGCTCGTGCCTGTAATCCCAGCACTTTGGGAGGCCAAG T C USP34 Ensembl:ENSG00000115464 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1236711355 Functional Loss SNV dbSNP153 33..33 33 - - - 45280 RMVar_ID_45280 Human_SNP_ID_74604947 A-to-I Human chr2 - 61454652 61454652 61454652 TTGGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACTTGGGAGGCGGAGGTTGAAGTGAGT TTGGCTACTCGGGAGGCTGAGGCAGGAGAATCCCTTGAACTTGGGAGGCGGAGGTTGAAGTGAGT T G USP34 Ensembl:ENSG00000115464 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1280688966 Functional Loss SNV dbSNP153 33..33 33 - - - 45281 RMVar_ID_45281 Human_SNP_ID_74609217 A-to-I Human chr2 - 61467055 61467055 61467055 GTGATCTACCCGCTTCCGTCTCCCAAAATGCTAGGATTACAGGCGTGAGCCACCGCGCCTGGCCA GTGATCTACCCGCTTCCGTCTCCCAAAATGCTGGGATTACAGGCGTGAGCCACCGCGCCTGGCCA T C USP34 Ensembl:ENSG00000115464 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs574623879 Functional Loss SNV dbSNP153 33..33 33 - - - 45282 RMVar_ID_45282 Human_SNP_ID_74609293 A-to-I Human chr2 - 61467243 61467243 61467243 GCTGGAGTGCAGTGGCACGGTTTCGGCTCACTACAACCTCTGCCTCCCTGGGTTCAGCAATTCTC GCTGGAGTGCAGTGGCACGGTTTCGGCTCACTGCAACCTCTGCCTCCCTGGGTTCAGCAATTCTC T C USP34 Ensembl:ENSG00000115464 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs964209870 Functional Loss SNV dbSNP153 33..33 33 - - - 45283 RMVar_ID_45283 Human_SNP_ID_74609578 A-to-I Human chr2 - 61467887 61467887 61467887 AACTCTGAATACAGCTCACGCCTGTATTCCCAACACTTTGGGAGGCCGAGGTGGGCGGATCACAA AACTCTGAATACAGCTCACGCCTGTATTCCCAGCACTTTGGGAGGCCGAGGTGGGCGGATCACAA T C USP34 Ensembl:ENSG00000115464 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1159934203 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13930990 45284 RMVar_ID_45284 Human_SNP_ID_74612654 A-to-I Human chr2 + 61475708 61475708 61475708 ATTGGGCTAATATTTATATTTTTAGTAGAGACAGGGATCTTACTATGTTGCCCAGGCTGTTCTTG ATTGGGCTAATATTTATATTTTTAGTAGAGACGGGGATCTTACTATGTTGCCCAGGCTGTTCTTG A G AC016727.1 Ensembl:ENSG00000270820 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1245231843 Functional Loss SNV dbSNP153 33..33 33 - - - 45285 RMVar_ID_45285 Human_SNP_ID_74612669 A-to-I Human chr2 + 61475752 61475752 61475752 ATGTTGCCCAGGCTGTTCTTGAACTCGGTCTCAAGTGATCCACCCACCTCAGCCTCCCAAAGTGA ATGTTGCCCAGGCTGTTCTTGAACTCGGTCTCCAGTGATCCACCCACCTCAGCCTCCCAAAGTGA A C AC016727.1 Ensembl:ENSG00000270820 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1203977465 Functional Loss SNV dbSNP153 33..33 33 - - - 45286 RMVar_ID_45286 Human_SNP_ID_74613872 A-to-I Human chr2 - 61479292 61479292 61479292 GCCTGTGCCACCATGCATGGCTAATTTTAGTAATGACAGGGTTTCACCATGTTGGCCAGGGTGGT GCCTGTGCCACCATGCATGGCTAATTTTAGTAGTGACAGGGTTTCACCATGTTGGCCAGGGTGGT T C XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1173703819 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81300,RMVar_hsa_circ_108881,RMVar_hsa_circ_99434,RMVar_hsa_circ_200498,RMVar_hsa_circ_200499,RMVar_hsa_circ_200500 45287 RMVar_ID_45287 Human_SNP_ID_74614270 A-to-I Human chr2 - 61480418 61480418 61480418 AAAATTAGCCAGGCGTGGTGGCGCACAGCTGTATTCGCAGCTACTTGAGAGGCTGAGGCAAGAGA AAAATTAGCCAGGCGTGGTGGCGCACAGCTGTCTTCGCAGCTACTTGAGAGGCTGAGGCAAGAGA T G XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1389654212 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81300,RMVar_hsa_circ_108881,RMVar_hsa_circ_99434,RMVar_hsa_circ_200498,RMVar_hsa_circ_200499,RMVar_hsa_circ_200500 45288 RMVar_ID_45288 Human_SNP_ID_74617135 A-to-I Human chr2 - 61488980 61488980 61488980 CTCCTGCCTCAACCTCCCGAGTAGGTGGGACTACAGGCGGCTGCCACCACGCCTGGCTATTTTTT CTCCTGCCTCAACCTCCCGAGTAGGTGGGACTTCAGGCGGCTGCCACCACGCCTGGCTATTTTTT T A XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1199892044 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1574,RMVar_hsa_circ_99434,RMVar_hsa_circ_265025,RMVar_hsa_circ_289503,RMVar_hsa_circ_200500,RMVar_hsa_circ_315608,RMVar_hsa_circ_355611,RMVar_hsa_circ_352064,RMVar_hsa_circ_61674,RMVar_hsa_circ_23408,RMVar_hsa_circ_200509,RMVar_hsa_circ_272166,RMVar_hsa_circ_200502,RMVar_hsa_circ_200504,RMVar_hsa_circ_200503,RMVar_hsa_circ_309105,RMVar_hsa_circ_316006,RMVar_hsa_circ_331444,RMVar_hsa_circ_302279,RMVar_hsa_circ_283246,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_200522,RMVar_hsa_circ_306485,RMVar_hsa_circ_200508,RMVar_hsa_circ_332879,RMVar_hsa_circ_311196,RMVar_hsa_circ_296615,RMVar_hsa_circ_298225,RMVar_hsa_circ_292172,RMVar_hsa_circ_112531,RMVar_hsa_circ_270043,RMVar_hsa_circ_200520,RMVar_hsa_circ_200521,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_78147,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_75681,RMVar_hsa_circ_287634,RMVar_hsa_circ_311324,RMVar_hsa_circ_200524,RMVar_hsa_circ_200525,RMVar_hsa_circ_327523,RMVar_hsa_circ_328911,RMVar_hsa_circ_297843,RMVar_hsa_circ_302621,RMVar_hsa_circ_110587,RMVar_hsa_circ_269964,RMVar_hsa_circ_106519,RMVar_hsa_circ_200530,RMVar_hsa_circ_200532,RMVar_hsa_circ_200534,RMVar_hsa_circ_200535,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_282625,RMVar_hsa_circ_316390,RMVar_hsa_circ_323336,RMVar_hsa_circ_331867,RMVar_hsa_circ_321705,RMVar_hsa_circ_311584,RMVar_hsa_circ_72981,RMVar_hsa_circ_53456,RMVar_hsa_circ_200540,RMVar_hsa_circ_200542,RMVar_hsa_circ_1921,RMVar_hsa_circ_200541,RMVar_hsa_circ_200539,RMVar_hsa_circ_74394,RMVar_hsa_circ_200537,RMVar_hsa_circ_264812 45289 RMVar_ID_45289 Human_SNP_ID_74617138 A-to-I Human chr2 - 61488990 61488990 61488990 TCACGCCGTTCTCCTGCCTCAACCTCCCGAGTAGGTGGGACTACAGGCGGCTGCCACCACGCCTG TCACGCCGTTCTCCTGCCTCAACCTCCCGAGTGGGTGGGACTACAGGCGGCTGCCACCACGCCTG T C XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1159716797 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1574,RMVar_hsa_circ_99434,RMVar_hsa_circ_265025,RMVar_hsa_circ_289503,RMVar_hsa_circ_200500,RMVar_hsa_circ_315608,RMVar_hsa_circ_355611,RMVar_hsa_circ_352064,RMVar_hsa_circ_61674,RMVar_hsa_circ_23408,RMVar_hsa_circ_200509,RMVar_hsa_circ_272166,RMVar_hsa_circ_200502,RMVar_hsa_circ_200504,RMVar_hsa_circ_200503,RMVar_hsa_circ_309105,RMVar_hsa_circ_316006,RMVar_hsa_circ_331444,RMVar_hsa_circ_302279,RMVar_hsa_circ_283246,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_200522,RMVar_hsa_circ_306485,RMVar_hsa_circ_200508,RMVar_hsa_circ_332879,RMVar_hsa_circ_311196,RMVar_hsa_circ_296615,RMVar_hsa_circ_298225,RMVar_hsa_circ_292172,RMVar_hsa_circ_112531,RMVar_hsa_circ_270043,RMVar_hsa_circ_200520,RMVar_hsa_circ_200521,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_78147,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_75681,RMVar_hsa_circ_287634,RMVar_hsa_circ_311324,RMVar_hsa_circ_200524,RMVar_hsa_circ_200525,RMVar_hsa_circ_327523,RMVar_hsa_circ_328911,RMVar_hsa_circ_297843,RMVar_hsa_circ_302621,RMVar_hsa_circ_110587,RMVar_hsa_circ_269964,RMVar_hsa_circ_106519,RMVar_hsa_circ_200530,RMVar_hsa_circ_200532,RMVar_hsa_circ_200534,RMVar_hsa_circ_200535,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_282625,RMVar_hsa_circ_316390,RMVar_hsa_circ_323336,RMVar_hsa_circ_331867,RMVar_hsa_circ_321705,RMVar_hsa_circ_311584,RMVar_hsa_circ_72981,RMVar_hsa_circ_53456,RMVar_hsa_circ_200540,RMVar_hsa_circ_200542,RMVar_hsa_circ_1921,RMVar_hsa_circ_200541,RMVar_hsa_circ_200539,RMVar_hsa_circ_74394,RMVar_hsa_circ_200537,RMVar_hsa_circ_264812 45290 RMVar_ID_45290 Human_SNP_ID_74617372 A-to-I Human chr2 - 61489617 61489617 61489617 CTGGGAGGCAGAGCTTGCAGTGAGCCGAGATCACGCCGCTGCACTCTAGCCTGGGCAACAGAACG CTGGGAGGCAGAGCTTGCAGTGAGCCGAGATCGCGCCGCTGCACTCTAGCCTGGGCAACAGAACG T C XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1056568512 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25590566 RMVar_hsa_circ_1574,RMVar_hsa_circ_99434,RMVar_hsa_circ_265025,RMVar_hsa_circ_289503,RMVar_hsa_circ_200500,RMVar_hsa_circ_315608,RMVar_hsa_circ_355611,RMVar_hsa_circ_352064,RMVar_hsa_circ_61674,RMVar_hsa_circ_23408,RMVar_hsa_circ_200509,RMVar_hsa_circ_272166,RMVar_hsa_circ_200502,RMVar_hsa_circ_200504,RMVar_hsa_circ_200503,RMVar_hsa_circ_309105,RMVar_hsa_circ_316006,RMVar_hsa_circ_331444,RMVar_hsa_circ_302279,RMVar_hsa_circ_283246,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_200522,RMVar_hsa_circ_306485,RMVar_hsa_circ_200508,RMVar_hsa_circ_332879,RMVar_hsa_circ_311196,RMVar_hsa_circ_296615,RMVar_hsa_circ_298225,RMVar_hsa_circ_292172,RMVar_hsa_circ_112531,RMVar_hsa_circ_270043,RMVar_hsa_circ_200520,RMVar_hsa_circ_200521,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_78147,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_75681,RMVar_hsa_circ_287634,RMVar_hsa_circ_311324,RMVar_hsa_circ_200524,RMVar_hsa_circ_200525,RMVar_hsa_circ_327523,RMVar_hsa_circ_328911,RMVar_hsa_circ_297843,RMVar_hsa_circ_302621,RMVar_hsa_circ_110587,RMVar_hsa_circ_269964,RMVar_hsa_circ_106519,RMVar_hsa_circ_200530,RMVar_hsa_circ_200532,RMVar_hsa_circ_200534,RMVar_hsa_circ_200535,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_282625,RMVar_hsa_circ_316390,RMVar_hsa_circ_323336,RMVar_hsa_circ_331867,RMVar_hsa_circ_321705,RMVar_hsa_circ_311584,RMVar_hsa_circ_72981,RMVar_hsa_circ_53456,RMVar_hsa_circ_200540,RMVar_hsa_circ_200542,RMVar_hsa_circ_1921,RMVar_hsa_circ_200541,RMVar_hsa_circ_200539,RMVar_hsa_circ_74394,RMVar_hsa_circ_200537,RMVar_hsa_circ_264812 45291 RMVar_ID_45291 Human_SNP_ID_74617420 A-to-I Human chr2 - 61489759 61489759 61489759 ACCAGGTCAGGGGATCGAGACCATCATGGCTAACGCAGTGAAACCCTGTCTCTACTAAAAATACA ACCAGGTCAGGGGATCGAGACCATCATGGCTACCGCAGTGAAACCCTGTCTCTACTAAAAATACA T G XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs924791052 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1574,RMVar_hsa_circ_99434,RMVar_hsa_circ_265025,RMVar_hsa_circ_289503,RMVar_hsa_circ_200500,RMVar_hsa_circ_315608,RMVar_hsa_circ_355611,RMVar_hsa_circ_352064,RMVar_hsa_circ_61674,RMVar_hsa_circ_23408,RMVar_hsa_circ_200509,RMVar_hsa_circ_272166,RMVar_hsa_circ_200502,RMVar_hsa_circ_200504,RMVar_hsa_circ_200503,RMVar_hsa_circ_309105,RMVar_hsa_circ_316006,RMVar_hsa_circ_331444,RMVar_hsa_circ_302279,RMVar_hsa_circ_283246,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_200522,RMVar_hsa_circ_306485,RMVar_hsa_circ_200508,RMVar_hsa_circ_332879,RMVar_hsa_circ_311196,RMVar_hsa_circ_296615,RMVar_hsa_circ_298225,RMVar_hsa_circ_292172,RMVar_hsa_circ_112531,RMVar_hsa_circ_270043,RMVar_hsa_circ_200520,RMVar_hsa_circ_200521,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_78147,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_75681,RMVar_hsa_circ_287634,RMVar_hsa_circ_311324,RMVar_hsa_circ_200524,RMVar_hsa_circ_200525,RMVar_hsa_circ_327523,RMVar_hsa_circ_328911,RMVar_hsa_circ_297843,RMVar_hsa_circ_302621,RMVar_hsa_circ_110587,RMVar_hsa_circ_269964,RMVar_hsa_circ_106519,RMVar_hsa_circ_200530,RMVar_hsa_circ_200532,RMVar_hsa_circ_200534,RMVar_hsa_circ_200535,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_282625,RMVar_hsa_circ_316390,RMVar_hsa_circ_323336,RMVar_hsa_circ_331867,RMVar_hsa_circ_321705,RMVar_hsa_circ_311584,RMVar_hsa_circ_72981,RMVar_hsa_circ_53456,RMVar_hsa_circ_200540,RMVar_hsa_circ_200542,RMVar_hsa_circ_1921,RMVar_hsa_circ_200541,RMVar_hsa_circ_200539,RMVar_hsa_circ_74394,RMVar_hsa_circ_200537,RMVar_hsa_circ_264812 45292 RMVar_ID_45292 Human_SNP_ID_74621597 A-to-I Human chr2 - 61503176 61503176 61503176 GAGGAGGGCGGATCACTTGAGGTCAGGAGTTCAAGATCAGCCTGGCCAACATGGTGAAACCTTGT GAGGAGGGCGGATCACTTGAGGTCAGGAGTTCTAGATCAGCCTGGCCAACATGGTGAAACCTTGT T A XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1280042610 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23182922 RMVar_hsa_circ_315608,RMVar_hsa_circ_3630,RMVar_hsa_circ_200502,RMVar_hsa_circ_331444,RMVar_hsa_circ_302279,RMVar_hsa_circ_200513,RMVar_hsa_circ_200514,RMVar_hsa_circ_311196,RMVar_hsa_circ_296615,RMVar_hsa_circ_200516,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_328911,RMVar_hsa_circ_302621,RMVar_hsa_circ_110587,RMVar_hsa_circ_200528,RMVar_hsa_circ_200527,RMVar_hsa_circ_200538,RMVar_hsa_circ_316390,RMVar_hsa_circ_311584,RMVar_hsa_circ_72981,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_295297,RMVar_hsa_circ_125221,RMVar_hsa_circ_116463,RMVar_hsa_circ_200543,RMVar_hsa_circ_200545,RMVar_hsa_circ_200544,RMVar_hsa_circ_308693,RMVar_hsa_circ_30436,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_101773,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_200561,RMVar_hsa_circ_333365,RMVar_hsa_circ_365112,RMVar_hsa_circ_200568,RMVar_hsa_circ_300366,RMVar_hsa_circ_310234,RMVar_hsa_circ_304877,RMVar_hsa_circ_200571,RMVar_hsa_circ_200569,RMVar_hsa_circ_200570,RMVar_hsa_circ_313513,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_200579,RMVar_hsa_circ_292485,RMVar_hsa_circ_311055,RMVar_hsa_circ_289892,RMVar_hsa_circ_20300,RMVar_hsa_circ_200586,RMVar_hsa_circ_200581,RMVar_hsa_circ_200582,RMVar_hsa_circ_326823,RMVar_hsa_circ_29379,RMVar_hsa_circ_281688,RMVar_hsa_circ_301783,RMVar_hsa_circ_200589,RMVar_hsa_circ_96676,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590 45293 RMVar_ID_45293 Human_SNP_ID_74621801 A-to-I Human chr2 - 61503842 61503842 61503842 GAAGTTTGGGCCAGGCCTGGTGGCTCATGCCTATAATCCCAGCAGTCTGGGAGGCCAAGGCAGGT GAAGTTTGGGCCAGGCCTGGTGGCTCATGCCTGTAATCCCAGCAGTCTGGGAGGCCAAGGCAGGT T C XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1002212131 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13931747,Human_RBP_ID_22477701 RMVar_hsa_circ_315608,RMVar_hsa_circ_3630,RMVar_hsa_circ_200502,RMVar_hsa_circ_331444,RMVar_hsa_circ_302279,RMVar_hsa_circ_200513,RMVar_hsa_circ_200514,RMVar_hsa_circ_311196,RMVar_hsa_circ_296615,RMVar_hsa_circ_200516,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_328911,RMVar_hsa_circ_302621,RMVar_hsa_circ_110587,RMVar_hsa_circ_200528,RMVar_hsa_circ_200527,RMVar_hsa_circ_200538,RMVar_hsa_circ_316390,RMVar_hsa_circ_311584,RMVar_hsa_circ_72981,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_295297,RMVar_hsa_circ_125221,RMVar_hsa_circ_116463,RMVar_hsa_circ_200543,RMVar_hsa_circ_200545,RMVar_hsa_circ_200544,RMVar_hsa_circ_308693,RMVar_hsa_circ_30436,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_101773,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_200561,RMVar_hsa_circ_333365,RMVar_hsa_circ_365112,RMVar_hsa_circ_200568,RMVar_hsa_circ_300366,RMVar_hsa_circ_310234,RMVar_hsa_circ_304877,RMVar_hsa_circ_200571,RMVar_hsa_circ_200569,RMVar_hsa_circ_200570,RMVar_hsa_circ_313513,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_200579,RMVar_hsa_circ_292485,RMVar_hsa_circ_311055,RMVar_hsa_circ_289892,RMVar_hsa_circ_20300,RMVar_hsa_circ_200586,RMVar_hsa_circ_200581,RMVar_hsa_circ_200582,RMVar_hsa_circ_326823,RMVar_hsa_circ_29379,RMVar_hsa_circ_281688,RMVar_hsa_circ_301783,RMVar_hsa_circ_200589,RMVar_hsa_circ_96676,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590 45294 RMVar_ID_45294 Human_SNP_ID_74621824 A-to-I Human chr2 - 61503936 61503936 61503936 GCCTCAAGCGATCCACCGGCTTCATCCTTCCAAAGTGCTGGGATTACAGGAGTAAGCCACTGTGC GCCTCAAGCGATCCACCGGCTTCATCCTTCCACAGTGCTGGGATTACAGGAGTAAGCCACTGTGC T G XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs987124810 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17570398,Human_RBP_ID_25556021 RMVar_hsa_circ_315608,RMVar_hsa_circ_3630,RMVar_hsa_circ_200502,RMVar_hsa_circ_331444,RMVar_hsa_circ_302279,RMVar_hsa_circ_200513,RMVar_hsa_circ_200514,RMVar_hsa_circ_311196,RMVar_hsa_circ_296615,RMVar_hsa_circ_200516,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_328911,RMVar_hsa_circ_302621,RMVar_hsa_circ_110587,RMVar_hsa_circ_200528,RMVar_hsa_circ_200527,RMVar_hsa_circ_200538,RMVar_hsa_circ_316390,RMVar_hsa_circ_311584,RMVar_hsa_circ_72981,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_295297,RMVar_hsa_circ_125221,RMVar_hsa_circ_116463,RMVar_hsa_circ_200543,RMVar_hsa_circ_200545,RMVar_hsa_circ_200544,RMVar_hsa_circ_308693,RMVar_hsa_circ_30436,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_101773,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_200561,RMVar_hsa_circ_333365,RMVar_hsa_circ_365112,RMVar_hsa_circ_200568,RMVar_hsa_circ_300366,RMVar_hsa_circ_310234,RMVar_hsa_circ_304877,RMVar_hsa_circ_200571,RMVar_hsa_circ_200569,RMVar_hsa_circ_200570,RMVar_hsa_circ_313513,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_200579,RMVar_hsa_circ_292485,RMVar_hsa_circ_311055,RMVar_hsa_circ_289892,RMVar_hsa_circ_20300,RMVar_hsa_circ_200586,RMVar_hsa_circ_200581,RMVar_hsa_circ_200582,RMVar_hsa_circ_326823,RMVar_hsa_circ_29379,RMVar_hsa_circ_281688,RMVar_hsa_circ_301783,RMVar_hsa_circ_200589,RMVar_hsa_circ_96676,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590 45295 RMVar_ID_45295 Human_SNP_ID_74622327 A-to-I Human chr2 - 61505719 61505719 61505719 CCCCATCTCTAGTGAAAATACAAAAAAAAGCCAGGTGCGGTGGCTCACGTCTGTAATCTCAGCAC CCCCATCTCTAGTGAAAATACAAAAAAAAGCCGGGTGCGGTGGCTCACGTCTGTAATCTCAGCAC T C XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs994075045 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13931850 RMVar_hsa_circ_315608,RMVar_hsa_circ_3630,RMVar_hsa_circ_200502,RMVar_hsa_circ_331444,RMVar_hsa_circ_302279,RMVar_hsa_circ_200513,RMVar_hsa_circ_200514,RMVar_hsa_circ_311196,RMVar_hsa_circ_296615,RMVar_hsa_circ_200516,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_328911,RMVar_hsa_circ_302621,RMVar_hsa_circ_110587,RMVar_hsa_circ_200528,RMVar_hsa_circ_200527,RMVar_hsa_circ_200538,RMVar_hsa_circ_316390,RMVar_hsa_circ_311584,RMVar_hsa_circ_72981,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_295297,RMVar_hsa_circ_125221,RMVar_hsa_circ_116463,RMVar_hsa_circ_200543,RMVar_hsa_circ_200545,RMVar_hsa_circ_200544,RMVar_hsa_circ_308693,RMVar_hsa_circ_30436,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_101773,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_200561,RMVar_hsa_circ_333365,RMVar_hsa_circ_365112,RMVar_hsa_circ_200568,RMVar_hsa_circ_300366,RMVar_hsa_circ_310234,RMVar_hsa_circ_304877,RMVar_hsa_circ_200571,RMVar_hsa_circ_200569,RMVar_hsa_circ_200570,RMVar_hsa_circ_313513,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_200579,RMVar_hsa_circ_292485,RMVar_hsa_circ_311055,RMVar_hsa_circ_289892,RMVar_hsa_circ_20300,RMVar_hsa_circ_200586,RMVar_hsa_circ_200581,RMVar_hsa_circ_200582,RMVar_hsa_circ_326823,RMVar_hsa_circ_29379,RMVar_hsa_circ_281688,RMVar_hsa_circ_301783,RMVar_hsa_circ_200589,RMVar_hsa_circ_96676,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590 45296 RMVar_ID_45296 Human_SNP_ID_74623097 A-to-I Human chr2 - 61508190 61508190 61508190 TTTTTTGAGATGGAGCCTCCCGCAGTAGAGATAGAGTTTCACTATGTTGGCCAGGCTGGTCTTGA TTTTTTGAGATGGAGCCTCCCGCAGTAGAGATGGAGTTTCACTATGTTGGCCAGGCTGGTCTTGA T C XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1196025157 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6936694,Human_RBP_ID_10008111,Human_RBP_ID_13931992,Human_RBP_ID_22999205,Human_RBP_ID_25590682 RMVar_hsa_circ_315608,RMVar_hsa_circ_3630,RMVar_hsa_circ_200502,RMVar_hsa_circ_331444,RMVar_hsa_circ_302279,RMVar_hsa_circ_200513,RMVar_hsa_circ_200514,RMVar_hsa_circ_311196,RMVar_hsa_circ_296615,RMVar_hsa_circ_200516,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_328911,RMVar_hsa_circ_302621,RMVar_hsa_circ_110587,RMVar_hsa_circ_200528,RMVar_hsa_circ_200527,RMVar_hsa_circ_200538,RMVar_hsa_circ_316390,RMVar_hsa_circ_311584,RMVar_hsa_circ_72981,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_295297,RMVar_hsa_circ_125221,RMVar_hsa_circ_116463,RMVar_hsa_circ_200543,RMVar_hsa_circ_200545,RMVar_hsa_circ_200544,RMVar_hsa_circ_308693,RMVar_hsa_circ_30436,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_101773,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_200561,RMVar_hsa_circ_333365,RMVar_hsa_circ_365112,RMVar_hsa_circ_200568,RMVar_hsa_circ_300366,RMVar_hsa_circ_310234,RMVar_hsa_circ_304877,RMVar_hsa_circ_200571,RMVar_hsa_circ_200569,RMVar_hsa_circ_200570,RMVar_hsa_circ_313513,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_200579,RMVar_hsa_circ_292485,RMVar_hsa_circ_311055,RMVar_hsa_circ_289892,RMVar_hsa_circ_20300,RMVar_hsa_circ_200586,RMVar_hsa_circ_200581,RMVar_hsa_circ_200582,RMVar_hsa_circ_326823,RMVar_hsa_circ_29379,RMVar_hsa_circ_281688,RMVar_hsa_circ_301783,RMVar_hsa_circ_200589,RMVar_hsa_circ_96676,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590 45297 RMVar_ID_45297 Human_SNP_ID_74623332 A-to-I Human chr2 - 61509130 61509130 61509130 GGGCGTGGTGACGGGCACCTGTAATCCCAGCTACTCTGGGAGGCTGAGGCAGGAGAATCGCTTGA GGGCGTGGTGACGGGCACCTGTAATCCCAGCTCCTCTGGGAGGCTGAGGCAGGAGAATCGCTTGA T G XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1470416264 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25556121 RMVar_hsa_circ_315608,RMVar_hsa_circ_3630,RMVar_hsa_circ_200502,RMVar_hsa_circ_331444,RMVar_hsa_circ_302279,RMVar_hsa_circ_200513,RMVar_hsa_circ_200514,RMVar_hsa_circ_311196,RMVar_hsa_circ_296615,RMVar_hsa_circ_200516,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_328911,RMVar_hsa_circ_302621,RMVar_hsa_circ_110587,RMVar_hsa_circ_200528,RMVar_hsa_circ_200527,RMVar_hsa_circ_200538,RMVar_hsa_circ_316390,RMVar_hsa_circ_311584,RMVar_hsa_circ_72981,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_295297,RMVar_hsa_circ_125221,RMVar_hsa_circ_116463,RMVar_hsa_circ_200543,RMVar_hsa_circ_200545,RMVar_hsa_circ_200544,RMVar_hsa_circ_308693,RMVar_hsa_circ_30436,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_101773,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_200561,RMVar_hsa_circ_333365,RMVar_hsa_circ_365112,RMVar_hsa_circ_200568,RMVar_hsa_circ_300366,RMVar_hsa_circ_310234,RMVar_hsa_circ_304877,RMVar_hsa_circ_200571,RMVar_hsa_circ_200569,RMVar_hsa_circ_200570,RMVar_hsa_circ_313513,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_200579,RMVar_hsa_circ_292485,RMVar_hsa_circ_311055,RMVar_hsa_circ_289892,RMVar_hsa_circ_20300,RMVar_hsa_circ_200586,RMVar_hsa_circ_200581,RMVar_hsa_circ_200582,RMVar_hsa_circ_326823,RMVar_hsa_circ_29379,RMVar_hsa_circ_281688,RMVar_hsa_circ_301783,RMVar_hsa_circ_200589,RMVar_hsa_circ_96676,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590 45298 RMVar_ID_45298 Human_SNP_ID_74623372 A-to-I Human chr2 - 61509251 61509251 61509251 CCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGTGGGTTGCCTGAGGTCAGGAGTTGGAGAAC CCTGTAATCCCAGCACTTTGGGAGGCTGAGGCCGGTGGGTTGCCTGAGGTCAGGAGTTGGAGAAC T G XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1290893053 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569268 RMVar_hsa_circ_315608,RMVar_hsa_circ_3630,RMVar_hsa_circ_200502,RMVar_hsa_circ_331444,RMVar_hsa_circ_302279,RMVar_hsa_circ_200513,RMVar_hsa_circ_200514,RMVar_hsa_circ_311196,RMVar_hsa_circ_296615,RMVar_hsa_circ_200516,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_328911,RMVar_hsa_circ_302621,RMVar_hsa_circ_110587,RMVar_hsa_circ_200528,RMVar_hsa_circ_200527,RMVar_hsa_circ_200538,RMVar_hsa_circ_316390,RMVar_hsa_circ_311584,RMVar_hsa_circ_72981,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_295297,RMVar_hsa_circ_125221,RMVar_hsa_circ_116463,RMVar_hsa_circ_200543,RMVar_hsa_circ_200545,RMVar_hsa_circ_200544,RMVar_hsa_circ_308693,RMVar_hsa_circ_30436,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_101773,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_200561,RMVar_hsa_circ_333365,RMVar_hsa_circ_365112,RMVar_hsa_circ_200568,RMVar_hsa_circ_300366,RMVar_hsa_circ_310234,RMVar_hsa_circ_304877,RMVar_hsa_circ_200571,RMVar_hsa_circ_200569,RMVar_hsa_circ_200570,RMVar_hsa_circ_313513,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_200579,RMVar_hsa_circ_292485,RMVar_hsa_circ_311055,RMVar_hsa_circ_289892,RMVar_hsa_circ_20300,RMVar_hsa_circ_200586,RMVar_hsa_circ_200581,RMVar_hsa_circ_200582,RMVar_hsa_circ_326823,RMVar_hsa_circ_29379,RMVar_hsa_circ_281688,RMVar_hsa_circ_301783,RMVar_hsa_circ_200589,RMVar_hsa_circ_96676,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590 45299 RMVar_ID_45299 Human_SNP_ID_74623426 A-to-I Human chr2 - 61509478 61509478 61509478 GGGATTACAGTCATGCGGCACCATGCCTGGCTAATTTTGTAGTTTTAGTAGAGACAGGGTTTCTT GGGATTACAGTCATGCGGCACCATGCCTGGCTCATTTTGTAGTTTTAGTAGAGACAGGGTTTCTT T G XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1204516123 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6936714,Human_RBP_ID_9992348,Human_RBP_ID_25556129 RMVar_hsa_circ_315608,RMVar_hsa_circ_3630,RMVar_hsa_circ_200502,RMVar_hsa_circ_331444,RMVar_hsa_circ_302279,RMVar_hsa_circ_200513,RMVar_hsa_circ_200514,RMVar_hsa_circ_311196,RMVar_hsa_circ_296615,RMVar_hsa_circ_200516,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_328911,RMVar_hsa_circ_302621,RMVar_hsa_circ_110587,RMVar_hsa_circ_200528,RMVar_hsa_circ_200527,RMVar_hsa_circ_200538,RMVar_hsa_circ_316390,RMVar_hsa_circ_311584,RMVar_hsa_circ_72981,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_295297,RMVar_hsa_circ_125221,RMVar_hsa_circ_116463,RMVar_hsa_circ_200543,RMVar_hsa_circ_200545,RMVar_hsa_circ_200544,RMVar_hsa_circ_308693,RMVar_hsa_circ_30436,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_101773,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_200561,RMVar_hsa_circ_333365,RMVar_hsa_circ_365112,RMVar_hsa_circ_200568,RMVar_hsa_circ_300366,RMVar_hsa_circ_310234,RMVar_hsa_circ_304877,RMVar_hsa_circ_200571,RMVar_hsa_circ_200569,RMVar_hsa_circ_200570,RMVar_hsa_circ_313513,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_200579,RMVar_hsa_circ_292485,RMVar_hsa_circ_311055,RMVar_hsa_circ_289892,RMVar_hsa_circ_20300,RMVar_hsa_circ_200586,RMVar_hsa_circ_200581,RMVar_hsa_circ_200582,RMVar_hsa_circ_326823,RMVar_hsa_circ_29379,RMVar_hsa_circ_281688,RMVar_hsa_circ_301783,RMVar_hsa_circ_200589,RMVar_hsa_circ_96676,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590 45300 RMVar_ID_45300 Human_SNP_ID_74623435 A-to-I Human chr2 - 61509504 61509504 61509504 CTCCTGCCTCATCCTCCTGTGTAGTTGGGATTACAGTCATGCGGCACCATGCCTGGCTAATTTTG CTCCTGCCTCATCCTCCTGTGTAGTTGGGATTGCAGTCATGCGGCACCATGCCTGGCTAATTTTG T C XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs554412904 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_315608,RMVar_hsa_circ_3630,RMVar_hsa_circ_200502,RMVar_hsa_circ_331444,RMVar_hsa_circ_302279,RMVar_hsa_circ_200513,RMVar_hsa_circ_200514,RMVar_hsa_circ_311196,RMVar_hsa_circ_296615,RMVar_hsa_circ_200516,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_328911,RMVar_hsa_circ_302621,RMVar_hsa_circ_110587,RMVar_hsa_circ_200528,RMVar_hsa_circ_200527,RMVar_hsa_circ_200538,RMVar_hsa_circ_316390,RMVar_hsa_circ_311584,RMVar_hsa_circ_72981,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_295297,RMVar_hsa_circ_125221,RMVar_hsa_circ_116463,RMVar_hsa_circ_200543,RMVar_hsa_circ_200545,RMVar_hsa_circ_200544,RMVar_hsa_circ_308693,RMVar_hsa_circ_30436,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_101773,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_200561,RMVar_hsa_circ_333365,RMVar_hsa_circ_365112,RMVar_hsa_circ_200568,RMVar_hsa_circ_300366,RMVar_hsa_circ_310234,RMVar_hsa_circ_304877,RMVar_hsa_circ_200571,RMVar_hsa_circ_200569,RMVar_hsa_circ_200570,RMVar_hsa_circ_313513,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_200579,RMVar_hsa_circ_292485,RMVar_hsa_circ_311055,RMVar_hsa_circ_289892,RMVar_hsa_circ_20300,RMVar_hsa_circ_200586,RMVar_hsa_circ_200581,RMVar_hsa_circ_200582,RMVar_hsa_circ_326823,RMVar_hsa_circ_29379,RMVar_hsa_circ_281688,RMVar_hsa_circ_301783,RMVar_hsa_circ_200589,RMVar_hsa_circ_96676,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590 45301 RMVar_ID_45301 Human_SNP_ID_74623604 A-to-I Human chr2 - 61510155 61510155 61510155 CTTGTGCCTCAGCCTCCAGAGTAGCTGGTACTACAGGTGTGCACCACCATGCCTGGCTATTTTTT CTTGTGCCTCAGCCTCCAGAGTAGCTGGTACTGCAGGTGTGCACCACCATGCCTGGCTATTTTTT T C XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs138550040 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_315608,RMVar_hsa_circ_3630,RMVar_hsa_circ_200502,RMVar_hsa_circ_331444,RMVar_hsa_circ_302279,RMVar_hsa_circ_200513,RMVar_hsa_circ_200514,RMVar_hsa_circ_311196,RMVar_hsa_circ_296615,RMVar_hsa_circ_200516,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_328911,RMVar_hsa_circ_302621,RMVar_hsa_circ_110587,RMVar_hsa_circ_200528,RMVar_hsa_circ_200527,RMVar_hsa_circ_200538,RMVar_hsa_circ_316390,RMVar_hsa_circ_311584,RMVar_hsa_circ_72981,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_295297,RMVar_hsa_circ_125221,RMVar_hsa_circ_116463,RMVar_hsa_circ_200543,RMVar_hsa_circ_200545,RMVar_hsa_circ_200544,RMVar_hsa_circ_308693,RMVar_hsa_circ_30436,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_101773,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_200561,RMVar_hsa_circ_333365,RMVar_hsa_circ_365112,RMVar_hsa_circ_200568,RMVar_hsa_circ_300366,RMVar_hsa_circ_310234,RMVar_hsa_circ_304877,RMVar_hsa_circ_200571,RMVar_hsa_circ_200569,RMVar_hsa_circ_200570,RMVar_hsa_circ_313513,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_200579,RMVar_hsa_circ_292485,RMVar_hsa_circ_311055,RMVar_hsa_circ_289892,RMVar_hsa_circ_20300,RMVar_hsa_circ_200586,RMVar_hsa_circ_200581,RMVar_hsa_circ_200582,RMVar_hsa_circ_326823,RMVar_hsa_circ_29379,RMVar_hsa_circ_281688,RMVar_hsa_circ_301783,RMVar_hsa_circ_200589,RMVar_hsa_circ_96676,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590 45302 RMVar_ID_45302 Human_SNP_ID_74624150 A-to-I Human chr2 - 61511923 61511923 61511923 TCTACTAAAAATACAAAAAAAATTAGCCGGGCATGGTGGCGTGTGCCTGTAATCCCAGAATCCCA TCTACTAAAAATACAAAAAAAATTAGCCGGGCGTGGTGGCGTGTGCCTGTAATCCCAGAATCCCA T C XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1359160526 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13932200 RMVar_hsa_circ_315608,RMVar_hsa_circ_3630,RMVar_hsa_circ_200502,RMVar_hsa_circ_331444,RMVar_hsa_circ_302279,RMVar_hsa_circ_200513,RMVar_hsa_circ_200514,RMVar_hsa_circ_311196,RMVar_hsa_circ_296615,RMVar_hsa_circ_200516,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_328911,RMVar_hsa_circ_302621,RMVar_hsa_circ_110587,RMVar_hsa_circ_200528,RMVar_hsa_circ_200527,RMVar_hsa_circ_200538,RMVar_hsa_circ_316390,RMVar_hsa_circ_311584,RMVar_hsa_circ_72981,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_295297,RMVar_hsa_circ_125221,RMVar_hsa_circ_116463,RMVar_hsa_circ_200543,RMVar_hsa_circ_200545,RMVar_hsa_circ_200544,RMVar_hsa_circ_308693,RMVar_hsa_circ_30436,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_101773,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_200561,RMVar_hsa_circ_333365,RMVar_hsa_circ_365112,RMVar_hsa_circ_200568,RMVar_hsa_circ_300366,RMVar_hsa_circ_310234,RMVar_hsa_circ_304877,RMVar_hsa_circ_200571,RMVar_hsa_circ_200569,RMVar_hsa_circ_200570,RMVar_hsa_circ_313513,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_200579,RMVar_hsa_circ_292485,RMVar_hsa_circ_311055,RMVar_hsa_circ_289892,RMVar_hsa_circ_20300,RMVar_hsa_circ_200586,RMVar_hsa_circ_200581,RMVar_hsa_circ_200582,RMVar_hsa_circ_326823,RMVar_hsa_circ_29379,RMVar_hsa_circ_281688,RMVar_hsa_circ_301783,RMVar_hsa_circ_200589,RMVar_hsa_circ_96676,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590 45303 RMVar_ID_45303 Human_SNP_ID_74624188 A-to-I Human chr2 - 61512050 61512050 61512050 AGAAATATACTTAATGCCTGGTGCGATGTCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCTAG AGAAATATACTTAATGCCTGGTGCGATGTCTCTCGCCTGTAATCCCAGCACTTTGGGAGGCCTAG T A XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1052753998 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13932202 RMVar_hsa_circ_315608,RMVar_hsa_circ_3630,RMVar_hsa_circ_200502,RMVar_hsa_circ_331444,RMVar_hsa_circ_302279,RMVar_hsa_circ_200513,RMVar_hsa_circ_200514,RMVar_hsa_circ_311196,RMVar_hsa_circ_296615,RMVar_hsa_circ_200516,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_328911,RMVar_hsa_circ_302621,RMVar_hsa_circ_110587,RMVar_hsa_circ_200528,RMVar_hsa_circ_200527,RMVar_hsa_circ_200538,RMVar_hsa_circ_316390,RMVar_hsa_circ_311584,RMVar_hsa_circ_72981,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_295297,RMVar_hsa_circ_125221,RMVar_hsa_circ_116463,RMVar_hsa_circ_200543,RMVar_hsa_circ_200545,RMVar_hsa_circ_200544,RMVar_hsa_circ_308693,RMVar_hsa_circ_30436,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_101773,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_200561,RMVar_hsa_circ_333365,RMVar_hsa_circ_365112,RMVar_hsa_circ_200568,RMVar_hsa_circ_300366,RMVar_hsa_circ_310234,RMVar_hsa_circ_304877,RMVar_hsa_circ_200571,RMVar_hsa_circ_200569,RMVar_hsa_circ_200570,RMVar_hsa_circ_313513,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_200579,RMVar_hsa_circ_292485,RMVar_hsa_circ_311055,RMVar_hsa_circ_289892,RMVar_hsa_circ_20300,RMVar_hsa_circ_200586,RMVar_hsa_circ_200581,RMVar_hsa_circ_200582,RMVar_hsa_circ_326823,RMVar_hsa_circ_29379,RMVar_hsa_circ_281688,RMVar_hsa_circ_301783,RMVar_hsa_circ_200589,RMVar_hsa_circ_96676,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590 45304 RMVar_ID_45304 Human_SNP_ID_74624362 A-to-I Human chr2 - 61512806 61512806 61512806 GAACTCCAGACCTCAAGTGATCCGCCAGTCTCAGCCTCCCAAAGTGCTGGGATTATGTGTGAGCT GAACTCCAGACCTCAAGTGATCCGCCAGTCTCGGCCTCCCAAAGTGCTGGGATTATGTGTGAGCT T C XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs879334326 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13932251,Human_RBP_ID_17569657 RMVar_hsa_circ_315608,RMVar_hsa_circ_3630,RMVar_hsa_circ_200502,RMVar_hsa_circ_331444,RMVar_hsa_circ_302279,RMVar_hsa_circ_200513,RMVar_hsa_circ_200514,RMVar_hsa_circ_311196,RMVar_hsa_circ_296615,RMVar_hsa_circ_200516,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_328911,RMVar_hsa_circ_302621,RMVar_hsa_circ_110587,RMVar_hsa_circ_200528,RMVar_hsa_circ_200527,RMVar_hsa_circ_200538,RMVar_hsa_circ_316390,RMVar_hsa_circ_311584,RMVar_hsa_circ_72981,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_295297,RMVar_hsa_circ_125221,RMVar_hsa_circ_116463,RMVar_hsa_circ_200543,RMVar_hsa_circ_200545,RMVar_hsa_circ_200544,RMVar_hsa_circ_308693,RMVar_hsa_circ_30436,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_101773,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_200561,RMVar_hsa_circ_333365,RMVar_hsa_circ_365112,RMVar_hsa_circ_200568,RMVar_hsa_circ_300366,RMVar_hsa_circ_310234,RMVar_hsa_circ_304877,RMVar_hsa_circ_200571,RMVar_hsa_circ_200569,RMVar_hsa_circ_200570,RMVar_hsa_circ_313513,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_200579,RMVar_hsa_circ_292485,RMVar_hsa_circ_311055,RMVar_hsa_circ_289892,RMVar_hsa_circ_20300,RMVar_hsa_circ_200586,RMVar_hsa_circ_200581,RMVar_hsa_circ_200582,RMVar_hsa_circ_326823,RMVar_hsa_circ_29379,RMVar_hsa_circ_281688,RMVar_hsa_circ_301783,RMVar_hsa_circ_200589,RMVar_hsa_circ_96676,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590 45305 RMVar_ID_45305 Human_SNP_ID_74624487 A-to-I Human chr2 - 61513219 61513219 61513219 AGGCAGGCGGAAACAATACAAACAAATTAGCCAGGCGTGGTGGCATGCACCTGTAATCCCGACTG AGGCAGGCGGAAACAATACAAACAAATTAGCCGGGCGTGGTGGCATGCACCTGTAATCCCGACTG T C XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1253156829 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_315608,RMVar_hsa_circ_3630,RMVar_hsa_circ_200502,RMVar_hsa_circ_331444,RMVar_hsa_circ_302279,RMVar_hsa_circ_200513,RMVar_hsa_circ_200514,RMVar_hsa_circ_311196,RMVar_hsa_circ_296615,RMVar_hsa_circ_200516,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_328911,RMVar_hsa_circ_302621,RMVar_hsa_circ_110587,RMVar_hsa_circ_200528,RMVar_hsa_circ_200527,RMVar_hsa_circ_200538,RMVar_hsa_circ_316390,RMVar_hsa_circ_311584,RMVar_hsa_circ_72981,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_295297,RMVar_hsa_circ_125221,RMVar_hsa_circ_116463,RMVar_hsa_circ_200543,RMVar_hsa_circ_200545,RMVar_hsa_circ_200544,RMVar_hsa_circ_308693,RMVar_hsa_circ_30436,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_101773,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_200561,RMVar_hsa_circ_333365,RMVar_hsa_circ_365112,RMVar_hsa_circ_200568,RMVar_hsa_circ_300366,RMVar_hsa_circ_310234,RMVar_hsa_circ_304877,RMVar_hsa_circ_200571,RMVar_hsa_circ_200569,RMVar_hsa_circ_200570,RMVar_hsa_circ_313513,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_200579,RMVar_hsa_circ_292485,RMVar_hsa_circ_311055,RMVar_hsa_circ_289892,RMVar_hsa_circ_20300,RMVar_hsa_circ_200586,RMVar_hsa_circ_200581,RMVar_hsa_circ_200582,RMVar_hsa_circ_326823,RMVar_hsa_circ_29379,RMVar_hsa_circ_281688,RMVar_hsa_circ_301783,RMVar_hsa_circ_200589,RMVar_hsa_circ_96676,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590 45306 RMVar_ID_45306 Human_SNP_ID_74624503 A-to-I Human chr2 - 61513288 61513288 61513288 TTTGCATTAAGATCTGTGATTTGGCTGGGCACAGTAGCTCACAATTGTAATCCCAGCACTGGGAG TTTGCATTAAGATCTGTGATTTGGCTGGGCACGGTAGCTCACAATTGTAATCCCAGCACTGGGAG T C XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs373683346 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_774718,Human_RBP_ID_6936755,Human_RBP_ID_13932265,Human_RBP_ID_17016890,Human_RBP_ID_25556198 RMVar_hsa_circ_315608,RMVar_hsa_circ_3630,RMVar_hsa_circ_200502,RMVar_hsa_circ_331444,RMVar_hsa_circ_302279,RMVar_hsa_circ_200513,RMVar_hsa_circ_200514,RMVar_hsa_circ_311196,RMVar_hsa_circ_296615,RMVar_hsa_circ_200516,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_328911,RMVar_hsa_circ_302621,RMVar_hsa_circ_110587,RMVar_hsa_circ_200528,RMVar_hsa_circ_200527,RMVar_hsa_circ_200538,RMVar_hsa_circ_316390,RMVar_hsa_circ_311584,RMVar_hsa_circ_72981,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_295297,RMVar_hsa_circ_125221,RMVar_hsa_circ_116463,RMVar_hsa_circ_200543,RMVar_hsa_circ_200545,RMVar_hsa_circ_200544,RMVar_hsa_circ_308693,RMVar_hsa_circ_30436,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_101773,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_200561,RMVar_hsa_circ_333365,RMVar_hsa_circ_365112,RMVar_hsa_circ_200568,RMVar_hsa_circ_300366,RMVar_hsa_circ_310234,RMVar_hsa_circ_304877,RMVar_hsa_circ_200571,RMVar_hsa_circ_200569,RMVar_hsa_circ_200570,RMVar_hsa_circ_313513,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_200579,RMVar_hsa_circ_292485,RMVar_hsa_circ_311055,RMVar_hsa_circ_289892,RMVar_hsa_circ_20300,RMVar_hsa_circ_200586,RMVar_hsa_circ_200581,RMVar_hsa_circ_200582,RMVar_hsa_circ_326823,RMVar_hsa_circ_29379,RMVar_hsa_circ_281688,RMVar_hsa_circ_301783,RMVar_hsa_circ_200589,RMVar_hsa_circ_96676,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590 45307 RMVar_ID_45307 Human_SNP_ID_74624594 A-to-I Human chr2 - 61513507 61513507 61513507 GAGCCTGGTCAACAGGGTGAAACCGCATGTCTACTAAAGATACAAAAATTAGCTGGGTGTGTTGG GAGCCTGGTCAACAGGGTGAAACCGCATGTCTGCTAAAGATACAAAAATTAGCTGGGTGTGTTGG T C XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs769645764 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_315608,RMVar_hsa_circ_3630,RMVar_hsa_circ_200502,RMVar_hsa_circ_331444,RMVar_hsa_circ_302279,RMVar_hsa_circ_200513,RMVar_hsa_circ_200514,RMVar_hsa_circ_311196,RMVar_hsa_circ_296615,RMVar_hsa_circ_200516,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_328911,RMVar_hsa_circ_302621,RMVar_hsa_circ_110587,RMVar_hsa_circ_200528,RMVar_hsa_circ_200527,RMVar_hsa_circ_200538,RMVar_hsa_circ_316390,RMVar_hsa_circ_311584,RMVar_hsa_circ_72981,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_295297,RMVar_hsa_circ_125221,RMVar_hsa_circ_116463,RMVar_hsa_circ_200543,RMVar_hsa_circ_200545,RMVar_hsa_circ_200544,RMVar_hsa_circ_308693,RMVar_hsa_circ_30436,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_101773,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_200561,RMVar_hsa_circ_333365,RMVar_hsa_circ_365112,RMVar_hsa_circ_200568,RMVar_hsa_circ_300366,RMVar_hsa_circ_310234,RMVar_hsa_circ_304877,RMVar_hsa_circ_200571,RMVar_hsa_circ_200569,RMVar_hsa_circ_200570,RMVar_hsa_circ_313513,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_200579,RMVar_hsa_circ_292485,RMVar_hsa_circ_311055,RMVar_hsa_circ_289892,RMVar_hsa_circ_20300,RMVar_hsa_circ_200586,RMVar_hsa_circ_200581,RMVar_hsa_circ_200582,RMVar_hsa_circ_326823,RMVar_hsa_circ_29379,RMVar_hsa_circ_281688,RMVar_hsa_circ_301783,RMVar_hsa_circ_200589,RMVar_hsa_circ_96676,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590 45308 RMVar_ID_45308 Human_SNP_ID_74624595 A-to-I Human chr2 - 61513507 61513507 61513507 GAGCCTGGTCAACAGGGTGAAACCGCATGTCTACTAAAGATACAAAAATTAGCTGGGTGTGTTGG GAGCCTGGTCAACAGGGTGAAACCGCATGTCTCCTAAAGATACAAAAATTAGCTGGGTGTGTTGG T G XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs769645764 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_315608,RMVar_hsa_circ_3630,RMVar_hsa_circ_200502,RMVar_hsa_circ_331444,RMVar_hsa_circ_302279,RMVar_hsa_circ_200513,RMVar_hsa_circ_200514,RMVar_hsa_circ_311196,RMVar_hsa_circ_296615,RMVar_hsa_circ_200516,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_328911,RMVar_hsa_circ_302621,RMVar_hsa_circ_110587,RMVar_hsa_circ_200528,RMVar_hsa_circ_200527,RMVar_hsa_circ_200538,RMVar_hsa_circ_316390,RMVar_hsa_circ_311584,RMVar_hsa_circ_72981,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_295297,RMVar_hsa_circ_125221,RMVar_hsa_circ_116463,RMVar_hsa_circ_200543,RMVar_hsa_circ_200545,RMVar_hsa_circ_200544,RMVar_hsa_circ_308693,RMVar_hsa_circ_30436,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_101773,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_200561,RMVar_hsa_circ_333365,RMVar_hsa_circ_365112,RMVar_hsa_circ_200568,RMVar_hsa_circ_300366,RMVar_hsa_circ_310234,RMVar_hsa_circ_304877,RMVar_hsa_circ_200571,RMVar_hsa_circ_200569,RMVar_hsa_circ_200570,RMVar_hsa_circ_313513,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_200579,RMVar_hsa_circ_292485,RMVar_hsa_circ_311055,RMVar_hsa_circ_289892,RMVar_hsa_circ_20300,RMVar_hsa_circ_200586,RMVar_hsa_circ_200581,RMVar_hsa_circ_200582,RMVar_hsa_circ_326823,RMVar_hsa_circ_29379,RMVar_hsa_circ_281688,RMVar_hsa_circ_301783,RMVar_hsa_circ_200589,RMVar_hsa_circ_96676,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590 45309 RMVar_ID_45309 Human_SNP_ID_74624734 A-to-I Human chr2 - 61513950 61513950 61513950 TCTATCTCCTGACCTCGTGATCCACCTGCCTCAGCCTCCCAAAGCGCTAGGATTACAGGCGTGTA TCTATCTCCTGACCTCGTGATCCACCTGCCTCCGCCTCCCAAAGCGCTAGGATTACAGGCGTGTA T G XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs778517022 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_315608,RMVar_hsa_circ_3630,RMVar_hsa_circ_200502,RMVar_hsa_circ_331444,RMVar_hsa_circ_302279,RMVar_hsa_circ_200513,RMVar_hsa_circ_200514,RMVar_hsa_circ_311196,RMVar_hsa_circ_296615,RMVar_hsa_circ_200516,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_328911,RMVar_hsa_circ_302621,RMVar_hsa_circ_110587,RMVar_hsa_circ_200528,RMVar_hsa_circ_200527,RMVar_hsa_circ_200538,RMVar_hsa_circ_316390,RMVar_hsa_circ_311584,RMVar_hsa_circ_72981,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_295297,RMVar_hsa_circ_125221,RMVar_hsa_circ_116463,RMVar_hsa_circ_200543,RMVar_hsa_circ_200545,RMVar_hsa_circ_200544,RMVar_hsa_circ_308693,RMVar_hsa_circ_30436,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_101773,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_200561,RMVar_hsa_circ_333365,RMVar_hsa_circ_365112,RMVar_hsa_circ_200568,RMVar_hsa_circ_300366,RMVar_hsa_circ_310234,RMVar_hsa_circ_304877,RMVar_hsa_circ_200571,RMVar_hsa_circ_200569,RMVar_hsa_circ_200570,RMVar_hsa_circ_313513,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_200579,RMVar_hsa_circ_292485,RMVar_hsa_circ_311055,RMVar_hsa_circ_289892,RMVar_hsa_circ_20300,RMVar_hsa_circ_200586,RMVar_hsa_circ_200581,RMVar_hsa_circ_200582,RMVar_hsa_circ_326823,RMVar_hsa_circ_29379,RMVar_hsa_circ_281688,RMVar_hsa_circ_301783,RMVar_hsa_circ_200589,RMVar_hsa_circ_96676,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590 45310 RMVar_ID_45310 Human_SNP_ID_74624803 A-to-I Human chr2 - 61514168 61514166 61514168 TTTTTTTTTTTTTTGAGACGGAGCCTGGCTCTATTGCCCCAGCTGGAGTGTGGTGGCACAATCTC TTTTTTTTTTTTTTGAGACGGAGCCTGGCTCT__TGCCCCAGCTGGAGTGTGGTGGCACAATCTC AAT A XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1236240540 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_242288,Human_RBP_ID_774719,Human_RBP_ID_13932308,Human_RBP_ID_20587235,Human_RBP_ID_25556219 RMVar_hsa_circ_315608,RMVar_hsa_circ_3630,RMVar_hsa_circ_200502,RMVar_hsa_circ_331444,RMVar_hsa_circ_302279,RMVar_hsa_circ_200513,RMVar_hsa_circ_200514,RMVar_hsa_circ_311196,RMVar_hsa_circ_296615,RMVar_hsa_circ_200516,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_328911,RMVar_hsa_circ_302621,RMVar_hsa_circ_110587,RMVar_hsa_circ_200528,RMVar_hsa_circ_200527,RMVar_hsa_circ_200538,RMVar_hsa_circ_316390,RMVar_hsa_circ_311584,RMVar_hsa_circ_72981,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_295297,RMVar_hsa_circ_125221,RMVar_hsa_circ_116463,RMVar_hsa_circ_200543,RMVar_hsa_circ_200545,RMVar_hsa_circ_200544,RMVar_hsa_circ_308693,RMVar_hsa_circ_30436,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_101773,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_200561,RMVar_hsa_circ_333365,RMVar_hsa_circ_365112,RMVar_hsa_circ_200568,RMVar_hsa_circ_300366,RMVar_hsa_circ_310234,RMVar_hsa_circ_304877,RMVar_hsa_circ_200571,RMVar_hsa_circ_200569,RMVar_hsa_circ_200570,RMVar_hsa_circ_313513,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_200579,RMVar_hsa_circ_292485,RMVar_hsa_circ_311055,RMVar_hsa_circ_289892,RMVar_hsa_circ_20300,RMVar_hsa_circ_200586,RMVar_hsa_circ_200581,RMVar_hsa_circ_200582,RMVar_hsa_circ_326823,RMVar_hsa_circ_29379,RMVar_hsa_circ_281688,RMVar_hsa_circ_301783,RMVar_hsa_circ_200589,RMVar_hsa_circ_96676,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590 45311 RMVar_ID_45311 Human_SNP_ID_74624804 A-to-I Human chr2 - 61514168 61514168 61514168 TTTTTTTTTTTTTTGAGACGGAGCCTGGCTCTATTGCCCCAGCTGGAGTGTGGTGGCACAATCTC TTTTTTTTTTTTTTGAGACGGAGCCTGGCTCTGTTGCCCCAGCTGGAGTGTGGTGGCACAATCTC T C XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1375607849 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_242288,Human_RBP_ID_774719,Human_RBP_ID_13932308,Human_RBP_ID_20587235,Human_RBP_ID_25556219 RMVar_hsa_circ_315608,RMVar_hsa_circ_3630,RMVar_hsa_circ_200502,RMVar_hsa_circ_331444,RMVar_hsa_circ_302279,RMVar_hsa_circ_200513,RMVar_hsa_circ_200514,RMVar_hsa_circ_311196,RMVar_hsa_circ_296615,RMVar_hsa_circ_200516,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_328911,RMVar_hsa_circ_302621,RMVar_hsa_circ_110587,RMVar_hsa_circ_200528,RMVar_hsa_circ_200527,RMVar_hsa_circ_200538,RMVar_hsa_circ_316390,RMVar_hsa_circ_311584,RMVar_hsa_circ_72981,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_295297,RMVar_hsa_circ_125221,RMVar_hsa_circ_116463,RMVar_hsa_circ_200543,RMVar_hsa_circ_200545,RMVar_hsa_circ_200544,RMVar_hsa_circ_308693,RMVar_hsa_circ_30436,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_101773,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_200561,RMVar_hsa_circ_333365,RMVar_hsa_circ_365112,RMVar_hsa_circ_200568,RMVar_hsa_circ_300366,RMVar_hsa_circ_310234,RMVar_hsa_circ_304877,RMVar_hsa_circ_200571,RMVar_hsa_circ_200569,RMVar_hsa_circ_200570,RMVar_hsa_circ_313513,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_200579,RMVar_hsa_circ_292485,RMVar_hsa_circ_311055,RMVar_hsa_circ_289892,RMVar_hsa_circ_20300,RMVar_hsa_circ_200586,RMVar_hsa_circ_200581,RMVar_hsa_circ_200582,RMVar_hsa_circ_326823,RMVar_hsa_circ_29379,RMVar_hsa_circ_281688,RMVar_hsa_circ_301783,RMVar_hsa_circ_200589,RMVar_hsa_circ_96676,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590 45312 RMVar_ID_45312 Human_SNP_ID_74624935 A-to-I Human chr2 - 61514536 61514532 61514536 CAGGCTGGAGTGCAGTGGCCTGATCTCGGCTGACTGCAACCTCTGTTTCCCGGGTTCAAGCGATT CAGGCTGGAGTGCAGTGGCCTGATCTCGGCTG____CAACCTCTGTTTCCCGGGTTCAAGCGATT GCAGT G XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1386560780 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_13932330 RMVar_hsa_circ_315608,RMVar_hsa_circ_3630,RMVar_hsa_circ_200502,RMVar_hsa_circ_331444,RMVar_hsa_circ_302279,RMVar_hsa_circ_200513,RMVar_hsa_circ_200514,RMVar_hsa_circ_311196,RMVar_hsa_circ_296615,RMVar_hsa_circ_200516,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_328911,RMVar_hsa_circ_302621,RMVar_hsa_circ_110587,RMVar_hsa_circ_200528,RMVar_hsa_circ_200527,RMVar_hsa_circ_200538,RMVar_hsa_circ_316390,RMVar_hsa_circ_311584,RMVar_hsa_circ_72981,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_295297,RMVar_hsa_circ_125221,RMVar_hsa_circ_116463,RMVar_hsa_circ_200543,RMVar_hsa_circ_200545,RMVar_hsa_circ_200544,RMVar_hsa_circ_308693,RMVar_hsa_circ_30436,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_101773,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_200561,RMVar_hsa_circ_333365,RMVar_hsa_circ_365112,RMVar_hsa_circ_200568,RMVar_hsa_circ_300366,RMVar_hsa_circ_310234,RMVar_hsa_circ_304877,RMVar_hsa_circ_200571,RMVar_hsa_circ_200569,RMVar_hsa_circ_200570,RMVar_hsa_circ_313513,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_200579,RMVar_hsa_circ_292485,RMVar_hsa_circ_311055,RMVar_hsa_circ_289892,RMVar_hsa_circ_20300,RMVar_hsa_circ_200586,RMVar_hsa_circ_200581,RMVar_hsa_circ_200582,RMVar_hsa_circ_326823,RMVar_hsa_circ_29379,RMVar_hsa_circ_281688,RMVar_hsa_circ_301783,RMVar_hsa_circ_200589,RMVar_hsa_circ_96676,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590 45313 RMVar_ID_45313 Human_SNP_ID_74624936 A-to-I Human chr2 - 61514536 61514536 61514536 CAGGCTGGAGTGCAGTGGCCTGATCTCGGCTGACTGCAACCTCTGTTTCCCGGGTTCAAGCGATT CAGGCTGGAGTGCAGTGGCCTGATCTCGGCTGCCTGCAACCTCTGTTTCCCGGGTTCAAGCGATT T G XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1464528873 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13932330 RMVar_hsa_circ_315608,RMVar_hsa_circ_3630,RMVar_hsa_circ_200502,RMVar_hsa_circ_331444,RMVar_hsa_circ_302279,RMVar_hsa_circ_200513,RMVar_hsa_circ_200514,RMVar_hsa_circ_311196,RMVar_hsa_circ_296615,RMVar_hsa_circ_200516,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_328911,RMVar_hsa_circ_302621,RMVar_hsa_circ_110587,RMVar_hsa_circ_200528,RMVar_hsa_circ_200527,RMVar_hsa_circ_200538,RMVar_hsa_circ_316390,RMVar_hsa_circ_311584,RMVar_hsa_circ_72981,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_295297,RMVar_hsa_circ_125221,RMVar_hsa_circ_116463,RMVar_hsa_circ_200543,RMVar_hsa_circ_200545,RMVar_hsa_circ_200544,RMVar_hsa_circ_308693,RMVar_hsa_circ_30436,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_101773,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_200561,RMVar_hsa_circ_333365,RMVar_hsa_circ_365112,RMVar_hsa_circ_200568,RMVar_hsa_circ_300366,RMVar_hsa_circ_310234,RMVar_hsa_circ_304877,RMVar_hsa_circ_200571,RMVar_hsa_circ_200569,RMVar_hsa_circ_200570,RMVar_hsa_circ_313513,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_200579,RMVar_hsa_circ_292485,RMVar_hsa_circ_311055,RMVar_hsa_circ_289892,RMVar_hsa_circ_20300,RMVar_hsa_circ_200586,RMVar_hsa_circ_200581,RMVar_hsa_circ_200582,RMVar_hsa_circ_326823,RMVar_hsa_circ_29379,RMVar_hsa_circ_281688,RMVar_hsa_circ_301783,RMVar_hsa_circ_200589,RMVar_hsa_circ_96676,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590 45314 RMVar_ID_45314 Human_SNP_ID_74625070 A-to-I Human chr2 - 61514890 61514890 61514890 TAATTTTTGTTTTTGTAATAGAGTTTCGCCATATTGGCCTGGCTGGTCTCAAACTCCCGACCTCA TAATTTTTGTTTTTGTAATAGAGTTTCGCCATGTTGGCCTGGCTGGTCTCAAACTCCCGACCTCA T C XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1028772988 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13932360,Human_RBP_ID_25556228 RMVar_hsa_circ_315608,RMVar_hsa_circ_3630,RMVar_hsa_circ_200502,RMVar_hsa_circ_331444,RMVar_hsa_circ_302279,RMVar_hsa_circ_200513,RMVar_hsa_circ_200514,RMVar_hsa_circ_311196,RMVar_hsa_circ_296615,RMVar_hsa_circ_200516,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_328911,RMVar_hsa_circ_302621,RMVar_hsa_circ_110587,RMVar_hsa_circ_200528,RMVar_hsa_circ_200527,RMVar_hsa_circ_200538,RMVar_hsa_circ_316390,RMVar_hsa_circ_311584,RMVar_hsa_circ_72981,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_295297,RMVar_hsa_circ_125221,RMVar_hsa_circ_116463,RMVar_hsa_circ_200543,RMVar_hsa_circ_200545,RMVar_hsa_circ_200544,RMVar_hsa_circ_308693,RMVar_hsa_circ_30436,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_101773,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_200561,RMVar_hsa_circ_333365,RMVar_hsa_circ_365112,RMVar_hsa_circ_200568,RMVar_hsa_circ_300366,RMVar_hsa_circ_310234,RMVar_hsa_circ_304877,RMVar_hsa_circ_200571,RMVar_hsa_circ_200569,RMVar_hsa_circ_200570,RMVar_hsa_circ_313513,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_200579,RMVar_hsa_circ_292485,RMVar_hsa_circ_311055,RMVar_hsa_circ_289892,RMVar_hsa_circ_20300,RMVar_hsa_circ_200586,RMVar_hsa_circ_200581,RMVar_hsa_circ_200582,RMVar_hsa_circ_326823,RMVar_hsa_circ_29379,RMVar_hsa_circ_281688,RMVar_hsa_circ_301783,RMVar_hsa_circ_200589,RMVar_hsa_circ_96676,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590 45315 RMVar_ID_45315 Human_SNP_ID_74625110 A-to-I Human chr2 - 61515006 61515006 61515006 GGAGTGCAGTGTCATGATCTTGGCTCATTGCAACCTCTGGCTCTCGGGTTCAAGCGATTCTTGTG GGAGTGCAGTGTCATGATCTTGGCTCATTGCACCCTCTGGCTCTCGGGTTCAAGCGATTCTTGTG T G XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,cerebellum - 29129909,30559470 RNA-Seq:(High) rs1236830529 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6936767,Human_RBP_ID_13932369 RMVar_hsa_circ_315608,RMVar_hsa_circ_3630,RMVar_hsa_circ_200502,RMVar_hsa_circ_331444,RMVar_hsa_circ_302279,RMVar_hsa_circ_200513,RMVar_hsa_circ_200514,RMVar_hsa_circ_311196,RMVar_hsa_circ_296615,RMVar_hsa_circ_200516,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_328911,RMVar_hsa_circ_302621,RMVar_hsa_circ_110587,RMVar_hsa_circ_200528,RMVar_hsa_circ_200527,RMVar_hsa_circ_200538,RMVar_hsa_circ_316390,RMVar_hsa_circ_311584,RMVar_hsa_circ_72981,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_295297,RMVar_hsa_circ_125221,RMVar_hsa_circ_116463,RMVar_hsa_circ_200543,RMVar_hsa_circ_200545,RMVar_hsa_circ_200544,RMVar_hsa_circ_308693,RMVar_hsa_circ_30436,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_101773,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_200561,RMVar_hsa_circ_333365,RMVar_hsa_circ_365112,RMVar_hsa_circ_200568,RMVar_hsa_circ_300366,RMVar_hsa_circ_310234,RMVar_hsa_circ_304877,RMVar_hsa_circ_200571,RMVar_hsa_circ_200569,RMVar_hsa_circ_200570,RMVar_hsa_circ_313513,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_200579,RMVar_hsa_circ_292485,RMVar_hsa_circ_311055,RMVar_hsa_circ_289892,RMVar_hsa_circ_20300,RMVar_hsa_circ_200586,RMVar_hsa_circ_200581,RMVar_hsa_circ_200582,RMVar_hsa_circ_326823,RMVar_hsa_circ_29379,RMVar_hsa_circ_281688,RMVar_hsa_circ_301783,RMVar_hsa_circ_200589,RMVar_hsa_circ_96676,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590 45316 RMVar_ID_45316 Human_SNP_ID_74625869 A-to-I Human chr2 - 61517014 61517014 61517014 CTTTAATCCCAGCTAATTGAGAGGCTGAGGCAAGAGAATCGGTTGAACCTGGGAGGTGGAGCTTA CTTTAATCCCAGCTAATTGAGAGGCTGAGGCAGGAGAATCGGTTGAACCTGGGAGGTGGAGCTTA T C XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1304224839 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13932485 RMVar_hsa_circ_315608,RMVar_hsa_circ_3630,RMVar_hsa_circ_200502,RMVar_hsa_circ_331444,RMVar_hsa_circ_302279,RMVar_hsa_circ_200513,RMVar_hsa_circ_200514,RMVar_hsa_circ_311196,RMVar_hsa_circ_296615,RMVar_hsa_circ_200516,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_328911,RMVar_hsa_circ_302621,RMVar_hsa_circ_110587,RMVar_hsa_circ_200528,RMVar_hsa_circ_200527,RMVar_hsa_circ_200538,RMVar_hsa_circ_316390,RMVar_hsa_circ_311584,RMVar_hsa_circ_72981,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_295297,RMVar_hsa_circ_125221,RMVar_hsa_circ_116463,RMVar_hsa_circ_200543,RMVar_hsa_circ_200545,RMVar_hsa_circ_200544,RMVar_hsa_circ_308693,RMVar_hsa_circ_30436,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_101773,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_200561,RMVar_hsa_circ_333365,RMVar_hsa_circ_365112,RMVar_hsa_circ_200568,RMVar_hsa_circ_300366,RMVar_hsa_circ_310234,RMVar_hsa_circ_304877,RMVar_hsa_circ_200571,RMVar_hsa_circ_200569,RMVar_hsa_circ_200570,RMVar_hsa_circ_313513,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_200579,RMVar_hsa_circ_292485,RMVar_hsa_circ_311055,RMVar_hsa_circ_289892,RMVar_hsa_circ_20300,RMVar_hsa_circ_200586,RMVar_hsa_circ_200581,RMVar_hsa_circ_200582,RMVar_hsa_circ_326823,RMVar_hsa_circ_29379,RMVar_hsa_circ_281688,RMVar_hsa_circ_301783,RMVar_hsa_circ_200589,RMVar_hsa_circ_96676,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590,RMVar_hsa_circ_200591,RMVar_hsa_circ_200592 45317 RMVar_ID_45317 Human_SNP_ID_74625885 A-to-I Human chr2 - 61517068 61517068 61517068 GAAACCCGGTCTCTACTAAAAATACCAAAATTAGCTGAGTGTGGTGGCAGATGCCTTTAATCCCA GAAACCCGGTCTCTACTAAAAATACCAAAATTCGCTGAGTGTGGTGGCAGATGCCTTTAATCCCA T G XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1031450679 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9992425,Human_RBP_ID_25556263 RMVar_hsa_circ_315608,RMVar_hsa_circ_3630,RMVar_hsa_circ_200502,RMVar_hsa_circ_331444,RMVar_hsa_circ_302279,RMVar_hsa_circ_200513,RMVar_hsa_circ_200514,RMVar_hsa_circ_311196,RMVar_hsa_circ_296615,RMVar_hsa_circ_200516,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_328911,RMVar_hsa_circ_302621,RMVar_hsa_circ_110587,RMVar_hsa_circ_200528,RMVar_hsa_circ_200527,RMVar_hsa_circ_200538,RMVar_hsa_circ_316390,RMVar_hsa_circ_311584,RMVar_hsa_circ_72981,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_295297,RMVar_hsa_circ_125221,RMVar_hsa_circ_116463,RMVar_hsa_circ_200543,RMVar_hsa_circ_200545,RMVar_hsa_circ_200544,RMVar_hsa_circ_308693,RMVar_hsa_circ_30436,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_101773,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_200561,RMVar_hsa_circ_333365,RMVar_hsa_circ_365112,RMVar_hsa_circ_200568,RMVar_hsa_circ_300366,RMVar_hsa_circ_310234,RMVar_hsa_circ_304877,RMVar_hsa_circ_200571,RMVar_hsa_circ_200569,RMVar_hsa_circ_200570,RMVar_hsa_circ_313513,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_200579,RMVar_hsa_circ_292485,RMVar_hsa_circ_311055,RMVar_hsa_circ_289892,RMVar_hsa_circ_20300,RMVar_hsa_circ_200586,RMVar_hsa_circ_200581,RMVar_hsa_circ_200582,RMVar_hsa_circ_326823,RMVar_hsa_circ_29379,RMVar_hsa_circ_281688,RMVar_hsa_circ_301783,RMVar_hsa_circ_200589,RMVar_hsa_circ_96676,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590,RMVar_hsa_circ_200591,RMVar_hsa_circ_200592 45318 RMVar_ID_45318 Human_SNP_ID_74625886 A-to-I Human chr2 - 61517071 61517071 61517071 GGTGAAACCCGGTCTCTACTAAAAATACCAAAATTAGCTGAGTGTGGTGGCAGATGCCTTTAATC GGTGAAACCCGGTCTCTACTAAAAATACCAAAGTTAGCTGAGTGTGGTGGCAGATGCCTTTAATC T C XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs576400433 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9992425,Human_RBP_ID_25556263 RMVar_hsa_circ_315608,RMVar_hsa_circ_3630,RMVar_hsa_circ_200502,RMVar_hsa_circ_331444,RMVar_hsa_circ_302279,RMVar_hsa_circ_200513,RMVar_hsa_circ_200514,RMVar_hsa_circ_311196,RMVar_hsa_circ_296615,RMVar_hsa_circ_200516,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_328911,RMVar_hsa_circ_302621,RMVar_hsa_circ_110587,RMVar_hsa_circ_200528,RMVar_hsa_circ_200527,RMVar_hsa_circ_200538,RMVar_hsa_circ_316390,RMVar_hsa_circ_311584,RMVar_hsa_circ_72981,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_295297,RMVar_hsa_circ_125221,RMVar_hsa_circ_116463,RMVar_hsa_circ_200543,RMVar_hsa_circ_200545,RMVar_hsa_circ_200544,RMVar_hsa_circ_308693,RMVar_hsa_circ_30436,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_101773,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_200561,RMVar_hsa_circ_333365,RMVar_hsa_circ_365112,RMVar_hsa_circ_200568,RMVar_hsa_circ_300366,RMVar_hsa_circ_310234,RMVar_hsa_circ_304877,RMVar_hsa_circ_200571,RMVar_hsa_circ_200569,RMVar_hsa_circ_200570,RMVar_hsa_circ_313513,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_200579,RMVar_hsa_circ_292485,RMVar_hsa_circ_311055,RMVar_hsa_circ_289892,RMVar_hsa_circ_20300,RMVar_hsa_circ_200586,RMVar_hsa_circ_200581,RMVar_hsa_circ_200582,RMVar_hsa_circ_326823,RMVar_hsa_circ_29379,RMVar_hsa_circ_281688,RMVar_hsa_circ_301783,RMVar_hsa_circ_200589,RMVar_hsa_circ_96676,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590,RMVar_hsa_circ_200591,RMVar_hsa_circ_200592 45319 RMVar_ID_45319 Human_SNP_ID_74625892 A-to-I Human chr2 - 61517083 61517083 61517083 CCTGGCCAGTGTGGTGAAACCCGGTCTCTACTAAAAATACCAAAATTAGCTGAGTGTGGTGGCAG CCTGGCCAGTGTGGTGAAACCCGGTCTCTACTGAAAATACCAAAATTAGCTGAGTGTGGTGGCAG T C XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1024160078 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9992425,Human_RBP_ID_25556263 RMVar_hsa_circ_315608,RMVar_hsa_circ_3630,RMVar_hsa_circ_200502,RMVar_hsa_circ_331444,RMVar_hsa_circ_302279,RMVar_hsa_circ_200513,RMVar_hsa_circ_200514,RMVar_hsa_circ_311196,RMVar_hsa_circ_296615,RMVar_hsa_circ_200516,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_328911,RMVar_hsa_circ_302621,RMVar_hsa_circ_110587,RMVar_hsa_circ_200528,RMVar_hsa_circ_200527,RMVar_hsa_circ_200538,RMVar_hsa_circ_316390,RMVar_hsa_circ_311584,RMVar_hsa_circ_72981,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_295297,RMVar_hsa_circ_125221,RMVar_hsa_circ_116463,RMVar_hsa_circ_200543,RMVar_hsa_circ_200545,RMVar_hsa_circ_200544,RMVar_hsa_circ_308693,RMVar_hsa_circ_30436,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_101773,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_200561,RMVar_hsa_circ_333365,RMVar_hsa_circ_365112,RMVar_hsa_circ_200568,RMVar_hsa_circ_300366,RMVar_hsa_circ_310234,RMVar_hsa_circ_304877,RMVar_hsa_circ_200571,RMVar_hsa_circ_200569,RMVar_hsa_circ_200570,RMVar_hsa_circ_313513,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_200579,RMVar_hsa_circ_292485,RMVar_hsa_circ_311055,RMVar_hsa_circ_289892,RMVar_hsa_circ_20300,RMVar_hsa_circ_200586,RMVar_hsa_circ_200581,RMVar_hsa_circ_200582,RMVar_hsa_circ_326823,RMVar_hsa_circ_29379,RMVar_hsa_circ_281688,RMVar_hsa_circ_301783,RMVar_hsa_circ_200589,RMVar_hsa_circ_96676,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590,RMVar_hsa_circ_200591,RMVar_hsa_circ_200592 45320 RMVar_ID_45320 Human_SNP_ID_74626007 A-to-I Human chr2 - 61517469 61517469 61517469 CAGTTACCACGCCTTAGCCTGCCAAAATAGCTAGGACTACAGGCATGTGCCACCACACCCAGCTA CAGTTACCACGCCTTAGCCTGCCAAAATAGCTGGGACTACAGGCATGTGCCACCACACCCAGCTA T C XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1361055707 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_315608,RMVar_hsa_circ_3630,RMVar_hsa_circ_200502,RMVar_hsa_circ_331444,RMVar_hsa_circ_302279,RMVar_hsa_circ_200513,RMVar_hsa_circ_200514,RMVar_hsa_circ_311196,RMVar_hsa_circ_296615,RMVar_hsa_circ_200516,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_328911,RMVar_hsa_circ_302621,RMVar_hsa_circ_110587,RMVar_hsa_circ_200528,RMVar_hsa_circ_200527,RMVar_hsa_circ_200538,RMVar_hsa_circ_316390,RMVar_hsa_circ_311584,RMVar_hsa_circ_72981,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_295297,RMVar_hsa_circ_125221,RMVar_hsa_circ_116463,RMVar_hsa_circ_200543,RMVar_hsa_circ_200545,RMVar_hsa_circ_200544,RMVar_hsa_circ_308693,RMVar_hsa_circ_30436,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_101773,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_200561,RMVar_hsa_circ_333365,RMVar_hsa_circ_365112,RMVar_hsa_circ_200568,RMVar_hsa_circ_300366,RMVar_hsa_circ_310234,RMVar_hsa_circ_304877,RMVar_hsa_circ_200571,RMVar_hsa_circ_200569,RMVar_hsa_circ_200570,RMVar_hsa_circ_313513,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_200579,RMVar_hsa_circ_292485,RMVar_hsa_circ_311055,RMVar_hsa_circ_289892,RMVar_hsa_circ_20300,RMVar_hsa_circ_200586,RMVar_hsa_circ_200581,RMVar_hsa_circ_200582,RMVar_hsa_circ_326823,RMVar_hsa_circ_29379,RMVar_hsa_circ_281688,RMVar_hsa_circ_301783,RMVar_hsa_circ_200589,RMVar_hsa_circ_96676,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590,RMVar_hsa_circ_200591,RMVar_hsa_circ_200592 45321 RMVar_ID_45321 Human_SNP_ID_74626105 A-to-I Human chr2 - 61517825 61517813 61517825 CCTGCCCTCTTGCCTCAGCCTTGAGAGTAGCTAGCACTGTAGGTCCGCACCACCATGCCCAGCTA CCTGCCCTCTTGCCTCAGCCTTGAGAGTAGCT____________CCGCACCACCATGCCCAGCTA GACCTACAGTGCT G XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1214171733 Functional Loss DEL dbSNP153 33..44 33 - - - Human_RBP_ID_6936806,Human_RBP_ID_9109420,Human_RBP_ID_13932542 RMVar_hsa_circ_315608,RMVar_hsa_circ_3630,RMVar_hsa_circ_200502,RMVar_hsa_circ_331444,RMVar_hsa_circ_302279,RMVar_hsa_circ_200513,RMVar_hsa_circ_200514,RMVar_hsa_circ_311196,RMVar_hsa_circ_296615,RMVar_hsa_circ_200516,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_328911,RMVar_hsa_circ_302621,RMVar_hsa_circ_110587,RMVar_hsa_circ_200528,RMVar_hsa_circ_200527,RMVar_hsa_circ_200538,RMVar_hsa_circ_316390,RMVar_hsa_circ_311584,RMVar_hsa_circ_72981,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_295297,RMVar_hsa_circ_125221,RMVar_hsa_circ_116463,RMVar_hsa_circ_200543,RMVar_hsa_circ_200545,RMVar_hsa_circ_200544,RMVar_hsa_circ_308693,RMVar_hsa_circ_30436,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_101773,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_200561,RMVar_hsa_circ_333365,RMVar_hsa_circ_365112,RMVar_hsa_circ_200568,RMVar_hsa_circ_300366,RMVar_hsa_circ_310234,RMVar_hsa_circ_304877,RMVar_hsa_circ_200571,RMVar_hsa_circ_200569,RMVar_hsa_circ_200570,RMVar_hsa_circ_313513,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_200579,RMVar_hsa_circ_292485,RMVar_hsa_circ_311055,RMVar_hsa_circ_289892,RMVar_hsa_circ_20300,RMVar_hsa_circ_200586,RMVar_hsa_circ_200581,RMVar_hsa_circ_200582,RMVar_hsa_circ_326823,RMVar_hsa_circ_29379,RMVar_hsa_circ_281688,RMVar_hsa_circ_301783,RMVar_hsa_circ_200589,RMVar_hsa_circ_96676,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590,RMVar_hsa_circ_200591,RMVar_hsa_circ_200592 45322 RMVar_ID_45322 Human_SNP_ID_74626107 A-to-I Human chr2 - 61517825 61517825 61517825 CCTGCCCTCTTGCCTCAGCCTTGAGAGTAGCTAGCACTGTAGGTCCGCACCACCATGCCCAGCTA CCTGCCCTCTTGCCTCAGCCTTGAGAGTAGCTGGCACTGTAGGTCCGCACCACCATGCCCAGCTA T C XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1217380023 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6936806,Human_RBP_ID_9109420,Human_RBP_ID_13932542 RMVar_hsa_circ_315608,RMVar_hsa_circ_3630,RMVar_hsa_circ_200502,RMVar_hsa_circ_331444,RMVar_hsa_circ_302279,RMVar_hsa_circ_200513,RMVar_hsa_circ_200514,RMVar_hsa_circ_311196,RMVar_hsa_circ_296615,RMVar_hsa_circ_200516,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_328911,RMVar_hsa_circ_302621,RMVar_hsa_circ_110587,RMVar_hsa_circ_200528,RMVar_hsa_circ_200527,RMVar_hsa_circ_200538,RMVar_hsa_circ_316390,RMVar_hsa_circ_311584,RMVar_hsa_circ_72981,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_295297,RMVar_hsa_circ_125221,RMVar_hsa_circ_116463,RMVar_hsa_circ_200543,RMVar_hsa_circ_200545,RMVar_hsa_circ_200544,RMVar_hsa_circ_308693,RMVar_hsa_circ_30436,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_101773,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_200561,RMVar_hsa_circ_333365,RMVar_hsa_circ_365112,RMVar_hsa_circ_200568,RMVar_hsa_circ_300366,RMVar_hsa_circ_310234,RMVar_hsa_circ_304877,RMVar_hsa_circ_200571,RMVar_hsa_circ_200569,RMVar_hsa_circ_200570,RMVar_hsa_circ_313513,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_200579,RMVar_hsa_circ_292485,RMVar_hsa_circ_311055,RMVar_hsa_circ_289892,RMVar_hsa_circ_20300,RMVar_hsa_circ_200586,RMVar_hsa_circ_200581,RMVar_hsa_circ_200582,RMVar_hsa_circ_326823,RMVar_hsa_circ_29379,RMVar_hsa_circ_281688,RMVar_hsa_circ_301783,RMVar_hsa_circ_200589,RMVar_hsa_circ_96676,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590,RMVar_hsa_circ_200591,RMVar_hsa_circ_200592 45323 RMVar_ID_45323 Human_SNP_ID_74626226 A-to-I Human chr2 - 61518217 61518217 61518217 GTAGGGTTTCACTCTGTTGCTCAGGCTGGAGTACAGTGGTGCAATCATGGTTCACTGCAGCCTGG GTAGGGTTTCACTCTGTTGCTCAGGCTGGAGTGCAGTGGTGCAATCATGGTTCACTGCAGCCTGG T C XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1050350297 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2655800,Human_RBP_ID_13932565,Human_RBP_ID_23878988,Human_RBP_ID_25556286 RMVar_hsa_circ_315608,RMVar_hsa_circ_3630,RMVar_hsa_circ_200502,RMVar_hsa_circ_331444,RMVar_hsa_circ_302279,RMVar_hsa_circ_200513,RMVar_hsa_circ_200514,RMVar_hsa_circ_311196,RMVar_hsa_circ_296615,RMVar_hsa_circ_200516,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_328911,RMVar_hsa_circ_302621,RMVar_hsa_circ_110587,RMVar_hsa_circ_200528,RMVar_hsa_circ_200527,RMVar_hsa_circ_200538,RMVar_hsa_circ_316390,RMVar_hsa_circ_311584,RMVar_hsa_circ_72981,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_295297,RMVar_hsa_circ_125221,RMVar_hsa_circ_116463,RMVar_hsa_circ_200543,RMVar_hsa_circ_200545,RMVar_hsa_circ_200544,RMVar_hsa_circ_308693,RMVar_hsa_circ_30436,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_101773,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_200561,RMVar_hsa_circ_333365,RMVar_hsa_circ_365112,RMVar_hsa_circ_200568,RMVar_hsa_circ_300366,RMVar_hsa_circ_310234,RMVar_hsa_circ_304877,RMVar_hsa_circ_200571,RMVar_hsa_circ_200569,RMVar_hsa_circ_200570,RMVar_hsa_circ_313513,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_200579,RMVar_hsa_circ_292485,RMVar_hsa_circ_311055,RMVar_hsa_circ_289892,RMVar_hsa_circ_20300,RMVar_hsa_circ_200586,RMVar_hsa_circ_200581,RMVar_hsa_circ_200582,RMVar_hsa_circ_326823,RMVar_hsa_circ_29379,RMVar_hsa_circ_281688,RMVar_hsa_circ_301783,RMVar_hsa_circ_200589,RMVar_hsa_circ_96676,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590,RMVar_hsa_circ_200591,RMVar_hsa_circ_200592 45324 RMVar_ID_45324 Human_SNP_ID_74626614 A-to-I Human chr2 - 61519154 61519154 61519154 ACGAGGTCAGGAGTTTGAGACCAGTCTTACCAACATGGAGAAACCCTATCTCTACTAAAAATACA ACGAGGTCAGGAGTTTGAGACCAGTCTTACCAGCATGGAGAAACCCTATCTCTACTAAAAATACA T C XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs958704493 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_315608,RMVar_hsa_circ_3630,RMVar_hsa_circ_200502,RMVar_hsa_circ_331444,RMVar_hsa_circ_302279,RMVar_hsa_circ_200513,RMVar_hsa_circ_200514,RMVar_hsa_circ_311196,RMVar_hsa_circ_296615,RMVar_hsa_circ_200516,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_328911,RMVar_hsa_circ_302621,RMVar_hsa_circ_110587,RMVar_hsa_circ_200528,RMVar_hsa_circ_200527,RMVar_hsa_circ_200538,RMVar_hsa_circ_316390,RMVar_hsa_circ_311584,RMVar_hsa_circ_72981,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_295297,RMVar_hsa_circ_125221,RMVar_hsa_circ_116463,RMVar_hsa_circ_200543,RMVar_hsa_circ_200545,RMVar_hsa_circ_200544,RMVar_hsa_circ_308693,RMVar_hsa_circ_30436,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_101773,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_200561,RMVar_hsa_circ_333365,RMVar_hsa_circ_365112,RMVar_hsa_circ_200568,RMVar_hsa_circ_300366,RMVar_hsa_circ_310234,RMVar_hsa_circ_304877,RMVar_hsa_circ_200571,RMVar_hsa_circ_200569,RMVar_hsa_circ_200570,RMVar_hsa_circ_313513,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_200579,RMVar_hsa_circ_292485,RMVar_hsa_circ_311055,RMVar_hsa_circ_289892,RMVar_hsa_circ_20300,RMVar_hsa_circ_200586,RMVar_hsa_circ_200581,RMVar_hsa_circ_200582,RMVar_hsa_circ_326823,RMVar_hsa_circ_29379,RMVar_hsa_circ_281688,RMVar_hsa_circ_301783,RMVar_hsa_circ_200589,RMVar_hsa_circ_96676,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590,RMVar_hsa_circ_200591,RMVar_hsa_circ_200592 45325 RMVar_ID_45325 Human_SNP_ID_74626710 A-to-I Human chr2 - 61519504 61519504 61519504 TTTTTAGTAGAGATGGTTTCACTATGTTAGCCAGGAAGGTCTCGATTTCCTGACCTTTTGGTCCT TTTTTAGTAGAGATGGTTTCACTATGTTAGCCGGGAAGGTCTCGATTTCCTGACCTTTTGGTCCT T C XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs941561906 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6936826,Human_RBP_ID_13932633,Human_RBP_ID_22252681 RMVar_hsa_circ_315608,RMVar_hsa_circ_3630,RMVar_hsa_circ_200502,RMVar_hsa_circ_331444,RMVar_hsa_circ_302279,RMVar_hsa_circ_200513,RMVar_hsa_circ_200514,RMVar_hsa_circ_311196,RMVar_hsa_circ_296615,RMVar_hsa_circ_200516,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_328911,RMVar_hsa_circ_302621,RMVar_hsa_circ_110587,RMVar_hsa_circ_200528,RMVar_hsa_circ_200527,RMVar_hsa_circ_200538,RMVar_hsa_circ_316390,RMVar_hsa_circ_311584,RMVar_hsa_circ_72981,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_295297,RMVar_hsa_circ_125221,RMVar_hsa_circ_116463,RMVar_hsa_circ_200543,RMVar_hsa_circ_200545,RMVar_hsa_circ_200544,RMVar_hsa_circ_308693,RMVar_hsa_circ_30436,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_101773,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_200561,RMVar_hsa_circ_333365,RMVar_hsa_circ_365112,RMVar_hsa_circ_200568,RMVar_hsa_circ_300366,RMVar_hsa_circ_310234,RMVar_hsa_circ_304877,RMVar_hsa_circ_200571,RMVar_hsa_circ_200569,RMVar_hsa_circ_200570,RMVar_hsa_circ_313513,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_200579,RMVar_hsa_circ_292485,RMVar_hsa_circ_311055,RMVar_hsa_circ_289892,RMVar_hsa_circ_20300,RMVar_hsa_circ_200586,RMVar_hsa_circ_200581,RMVar_hsa_circ_200582,RMVar_hsa_circ_326823,RMVar_hsa_circ_29379,RMVar_hsa_circ_281688,RMVar_hsa_circ_301783,RMVar_hsa_circ_200589,RMVar_hsa_circ_96676,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590,RMVar_hsa_circ_200591,RMVar_hsa_circ_200592 45326 RMVar_ID_45326 Human_SNP_ID_74626753 A-to-I Human chr2 - 61519642 61519642 61519642 CAGGCTGGAGTGCAGTGGCGCAGTCTTGGCTCACTGCAAGCTCCACCTCCTGGGTTCATGCCATT CAGGCTGGAGTGCAGTGGCGCAGTCTTGGCTCCCTGCAAGCTCCACCTCCTGGGTTCATGCCATT T G XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1406720595 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_315608,RMVar_hsa_circ_3630,RMVar_hsa_circ_200502,RMVar_hsa_circ_331444,RMVar_hsa_circ_302279,RMVar_hsa_circ_200513,RMVar_hsa_circ_200514,RMVar_hsa_circ_311196,RMVar_hsa_circ_296615,RMVar_hsa_circ_200516,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_328911,RMVar_hsa_circ_302621,RMVar_hsa_circ_110587,RMVar_hsa_circ_200528,RMVar_hsa_circ_200527,RMVar_hsa_circ_200538,RMVar_hsa_circ_316390,RMVar_hsa_circ_311584,RMVar_hsa_circ_72981,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_295297,RMVar_hsa_circ_125221,RMVar_hsa_circ_116463,RMVar_hsa_circ_200543,RMVar_hsa_circ_200545,RMVar_hsa_circ_200544,RMVar_hsa_circ_308693,RMVar_hsa_circ_30436,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_101773,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_200561,RMVar_hsa_circ_333365,RMVar_hsa_circ_365112,RMVar_hsa_circ_200568,RMVar_hsa_circ_300366,RMVar_hsa_circ_310234,RMVar_hsa_circ_304877,RMVar_hsa_circ_200571,RMVar_hsa_circ_200569,RMVar_hsa_circ_200570,RMVar_hsa_circ_313513,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_200579,RMVar_hsa_circ_292485,RMVar_hsa_circ_311055,RMVar_hsa_circ_289892,RMVar_hsa_circ_20300,RMVar_hsa_circ_200586,RMVar_hsa_circ_200581,RMVar_hsa_circ_200582,RMVar_hsa_circ_326823,RMVar_hsa_circ_29379,RMVar_hsa_circ_281688,RMVar_hsa_circ_301783,RMVar_hsa_circ_200589,RMVar_hsa_circ_96676,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590,RMVar_hsa_circ_200591,RMVar_hsa_circ_200592 45327 RMVar_ID_45327 Human_SNP_ID_74627518 A-to-I Human chr2 - 61521957 61521957 61521957 GGCCAGAAGTTTGAGACCATCCTGGGTAACATAGCGAGACCCTGTGTTTACAAAAAATTTAAAAA GGCCAGAAGTTTGAGACCATCCTGGGTAACATGGCGAGACCCTGTGTTTACAAAAAATTTAAAAA T C XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1411348963 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_315608,RMVar_hsa_circ_3630,RMVar_hsa_circ_200502,RMVar_hsa_circ_331444,RMVar_hsa_circ_302279,RMVar_hsa_circ_200513,RMVar_hsa_circ_200514,RMVar_hsa_circ_311196,RMVar_hsa_circ_296615,RMVar_hsa_circ_200516,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_328911,RMVar_hsa_circ_302621,RMVar_hsa_circ_110587,RMVar_hsa_circ_200528,RMVar_hsa_circ_200527,RMVar_hsa_circ_200538,RMVar_hsa_circ_316390,RMVar_hsa_circ_311584,RMVar_hsa_circ_72981,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_295297,RMVar_hsa_circ_125221,RMVar_hsa_circ_116463,RMVar_hsa_circ_200543,RMVar_hsa_circ_200545,RMVar_hsa_circ_200544,RMVar_hsa_circ_308693,RMVar_hsa_circ_30436,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_101773,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_200561,RMVar_hsa_circ_333365,RMVar_hsa_circ_365112,RMVar_hsa_circ_200568,RMVar_hsa_circ_300366,RMVar_hsa_circ_310234,RMVar_hsa_circ_304877,RMVar_hsa_circ_200571,RMVar_hsa_circ_200569,RMVar_hsa_circ_200570,RMVar_hsa_circ_313513,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_200579,RMVar_hsa_circ_292485,RMVar_hsa_circ_311055,RMVar_hsa_circ_289892,RMVar_hsa_circ_20300,RMVar_hsa_circ_200586,RMVar_hsa_circ_200581,RMVar_hsa_circ_200582,RMVar_hsa_circ_326823,RMVar_hsa_circ_29379,RMVar_hsa_circ_281688,RMVar_hsa_circ_301783,RMVar_hsa_circ_200589,RMVar_hsa_circ_96676,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590,RMVar_hsa_circ_200591,RMVar_hsa_circ_200592 45328 RMVar_ID_45328 Human_SNP_ID_74628799 A-to-I Human chr2 - 61526983 61526983 61526983 TAGGAGTTGGCTGGGCATGGTGGCTCACTCCTATAATCTCAGCACTTTGGGAGGCCAAGGCAGGC TAGGAGTTGGCTGGGCATGGTGGCTCACTCCTGTAATCTCAGCACTTTGGGAGGCCAAGGCAGGC T C XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs978321047 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_315608,RMVar_hsa_circ_200502,RMVar_hsa_circ_302279,RMVar_hsa_circ_200514,RMVar_hsa_circ_296615,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_302621,RMVar_hsa_circ_316390,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_200543,RMVar_hsa_circ_308693,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_333365,RMVar_hsa_circ_200568,RMVar_hsa_circ_304877,RMVar_hsa_circ_200569,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_289892,RMVar_hsa_circ_98453,RMVar_hsa_circ_200581,RMVar_hsa_circ_326823,RMVar_hsa_circ_301783,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590,RMVar_hsa_circ_278039,RMVar_hsa_circ_200594,RMVar_hsa_circ_200595,RMVar_hsa_circ_18859,RMVar_hsa_circ_200593,RMVar_hsa_circ_200600,RMVar_hsa_circ_297031 45329 RMVar_ID_45329 Human_SNP_ID_74628942 A-to-I Human chr2 - 61527393 61527393 61527393 ACCTTGATTTCCAGGGCTCAAGTGATCCTCCCATCTCGGTCTCCTGAGTAGTTAGGACTATAGGT ACCTTGATTTCCAGGGCTCAAGTGATCCTCCCGTCTCGGTCTCCTGAGTAGTTAGGACTATAGGT T C XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs576538232 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13933105 RMVar_hsa_circ_315608,RMVar_hsa_circ_200502,RMVar_hsa_circ_302279,RMVar_hsa_circ_200514,RMVar_hsa_circ_296615,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_302621,RMVar_hsa_circ_316390,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_200543,RMVar_hsa_circ_308693,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_333365,RMVar_hsa_circ_200568,RMVar_hsa_circ_304877,RMVar_hsa_circ_200569,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_289892,RMVar_hsa_circ_98453,RMVar_hsa_circ_200581,RMVar_hsa_circ_326823,RMVar_hsa_circ_301783,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590,RMVar_hsa_circ_278039,RMVar_hsa_circ_200594,RMVar_hsa_circ_200595,RMVar_hsa_circ_18859,RMVar_hsa_circ_200593,RMVar_hsa_circ_200600,RMVar_hsa_circ_297031 45330 RMVar_ID_45330 Human_SNP_ID_74628983 A-to-I Human chr2 - 61527483 61527481 61527483 GTAGGTGTGCTTTTTTTTGTTTTTCTAGAGACAGGGTCTCTGCTCTTTCACCCAGGCTGAAGTGT GTAGGTGTGCTTTTTTTTGTTTTTCTAGAGAC__GGTCTCTGCTCTTTCACCCAGGCTGAAGTGT CCT C XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE38233;GSE100210;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,temporal_cortex - 24183664,29129909,30559470 RNA-Seq:(High) rs1006922621 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_774728,Human_RBP_ID_3630495,Human_RBP_ID_6937013,Human_RBP_ID_13933115 RMVar_hsa_circ_315608,RMVar_hsa_circ_200502,RMVar_hsa_circ_302279,RMVar_hsa_circ_200514,RMVar_hsa_circ_296615,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_302621,RMVar_hsa_circ_316390,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_200543,RMVar_hsa_circ_308693,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_333365,RMVar_hsa_circ_200568,RMVar_hsa_circ_304877,RMVar_hsa_circ_200569,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_289892,RMVar_hsa_circ_98453,RMVar_hsa_circ_200581,RMVar_hsa_circ_326823,RMVar_hsa_circ_301783,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590,RMVar_hsa_circ_278039,RMVar_hsa_circ_200594,RMVar_hsa_circ_200595,RMVar_hsa_circ_18859,RMVar_hsa_circ_200593,RMVar_hsa_circ_200600,RMVar_hsa_circ_297031 45331 RMVar_ID_45331 Human_SNP_ID_74629174 A-to-I Human chr2 - 61528100 61528100 61528100 CAATACAGTGAAACCCTGTCTCTACTGAAAATACAAAAATTAGCCAGGCGTGGTGGCAGGTGCCT CAATACAGTGAAACCCTGTCTCTACTGAAAATTCAAAAATTAGCCAGGCGTGGTGGCAGGTGCCT T A XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs13411269 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_315608,RMVar_hsa_circ_200502,RMVar_hsa_circ_302279,RMVar_hsa_circ_200514,RMVar_hsa_circ_296615,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_302621,RMVar_hsa_circ_316390,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_200543,RMVar_hsa_circ_308693,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_333365,RMVar_hsa_circ_200568,RMVar_hsa_circ_304877,RMVar_hsa_circ_200569,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_289892,RMVar_hsa_circ_98453,RMVar_hsa_circ_200581,RMVar_hsa_circ_326823,RMVar_hsa_circ_301783,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590,RMVar_hsa_circ_278039,RMVar_hsa_circ_200594,RMVar_hsa_circ_200595,RMVar_hsa_circ_18859,RMVar_hsa_circ_200593,RMVar_hsa_circ_200600,RMVar_hsa_circ_297031 45332 RMVar_ID_45332 Human_SNP_ID_74629186 A-to-I Human chr2 - 61528126 61528126 61528126 GGTCAGGAGTTCAAGACCAGCCTGGCCAATACAGTGAAACCCTGTCTCTACTGAAAATACAAAAA GGTCAGGAGTTCAAGACCAGCCTGGCCAATACGGTGAAACCCTGTCTCTACTGAAAATACAAAAA T C XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1028360445 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_315608,RMVar_hsa_circ_200502,RMVar_hsa_circ_302279,RMVar_hsa_circ_200514,RMVar_hsa_circ_296615,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_302621,RMVar_hsa_circ_316390,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_200543,RMVar_hsa_circ_308693,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_333365,RMVar_hsa_circ_200568,RMVar_hsa_circ_304877,RMVar_hsa_circ_200569,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_289892,RMVar_hsa_circ_98453,RMVar_hsa_circ_200581,RMVar_hsa_circ_326823,RMVar_hsa_circ_301783,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590,RMVar_hsa_circ_278039,RMVar_hsa_circ_200594,RMVar_hsa_circ_200595,RMVar_hsa_circ_18859,RMVar_hsa_circ_200593,RMVar_hsa_circ_200600,RMVar_hsa_circ_297031 45333 RMVar_ID_45333 Human_SNP_ID_74629299 A-to-I Human chr2 - 61528450 61528442 61528450 TTTTGTATTTTTAGTAGAGATGGGGTTTCGCCATATTGGTCAGGATGGTCTTGAACTCCTGACCT TTTTGTATTTTTAGTAGAGATGGGGTTTCGCC________CAGGATGGTCTTGAACTCCTGACCT GACCAATAT G XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1478289850 Functional Loss DEL dbSNP153 33..40 33 - - - Human_RBP_ID_13933168 RMVar_hsa_circ_315608,RMVar_hsa_circ_200502,RMVar_hsa_circ_302279,RMVar_hsa_circ_200514,RMVar_hsa_circ_296615,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_302621,RMVar_hsa_circ_316390,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_200543,RMVar_hsa_circ_308693,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_333365,RMVar_hsa_circ_200568,RMVar_hsa_circ_304877,RMVar_hsa_circ_200569,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_289892,RMVar_hsa_circ_98453,RMVar_hsa_circ_200581,RMVar_hsa_circ_326823,RMVar_hsa_circ_301783,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590,RMVar_hsa_circ_278039,RMVar_hsa_circ_200594,RMVar_hsa_circ_200595,RMVar_hsa_circ_18859,RMVar_hsa_circ_200593,RMVar_hsa_circ_200600,RMVar_hsa_circ_297031 45334 RMVar_ID_45334 Human_SNP_ID_74629302 A-to-I Human chr2 - 61528448 61528448 61528448 TTGTATTTTTAGTAGAGATGGGGTTTCGCCATATTGGTCAGGATGGTCTTGAACTCCTGACCTTG TTGTATTTTTAGTAGAGATGGGGTTTCGCCATGTTGGTCAGGATGGTCTTGAACTCCTGACCTTG T C XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1248243176 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13933168,Human_RBP_ID_25556448 RMVar_hsa_circ_315608,RMVar_hsa_circ_200502,RMVar_hsa_circ_302279,RMVar_hsa_circ_200514,RMVar_hsa_circ_296615,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_302621,RMVar_hsa_circ_316390,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_200543,RMVar_hsa_circ_308693,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_333365,RMVar_hsa_circ_200568,RMVar_hsa_circ_304877,RMVar_hsa_circ_200569,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_289892,RMVar_hsa_circ_98453,RMVar_hsa_circ_200581,RMVar_hsa_circ_326823,RMVar_hsa_circ_301783,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590,RMVar_hsa_circ_278039,RMVar_hsa_circ_200594,RMVar_hsa_circ_200595,RMVar_hsa_circ_18859,RMVar_hsa_circ_200593,RMVar_hsa_circ_200600,RMVar_hsa_circ_297031 45335 RMVar_ID_45335 Human_SNP_ID_74629309 A-to-I Human chr2 - 61528467 61528467 61528467 CACCATTCCCGGCTAGTTTTTGTATTTTTAGTAGAGATGGGGTTTCGCCATATTGGTCAGGATGG CACCATTCCCGGCTAGTTTTTGTATTTTTAGTGGAGATGGGGTTTCGCCATATTGGTCAGGATGG T C XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1262537968 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13933168 RMVar_hsa_circ_315608,RMVar_hsa_circ_200502,RMVar_hsa_circ_302279,RMVar_hsa_circ_200514,RMVar_hsa_circ_296615,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_302621,RMVar_hsa_circ_316390,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_200543,RMVar_hsa_circ_308693,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_333365,RMVar_hsa_circ_200568,RMVar_hsa_circ_304877,RMVar_hsa_circ_200569,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_289892,RMVar_hsa_circ_98453,RMVar_hsa_circ_200581,RMVar_hsa_circ_326823,RMVar_hsa_circ_301783,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590,RMVar_hsa_circ_278039,RMVar_hsa_circ_200594,RMVar_hsa_circ_200595,RMVar_hsa_circ_18859,RMVar_hsa_circ_200593,RMVar_hsa_circ_200600,RMVar_hsa_circ_297031 45336 RMVar_ID_45336 Human_SNP_ID_74629335 A-to-I Human chr2 - 61528550 61528550 61528550 TTGGCTCACTGCAACCTCCGCTCCTGGATTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCT TTGGCTCACTGCAACCTCCGCTCCTGGATTCAGGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCT T C XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1052031632 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6937023 RMVar_hsa_circ_315608,RMVar_hsa_circ_200502,RMVar_hsa_circ_302279,RMVar_hsa_circ_200514,RMVar_hsa_circ_296615,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_302621,RMVar_hsa_circ_316390,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_200543,RMVar_hsa_circ_308693,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_333365,RMVar_hsa_circ_200568,RMVar_hsa_circ_304877,RMVar_hsa_circ_200569,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_289892,RMVar_hsa_circ_98453,RMVar_hsa_circ_200581,RMVar_hsa_circ_326823,RMVar_hsa_circ_301783,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590,RMVar_hsa_circ_278039,RMVar_hsa_circ_200594,RMVar_hsa_circ_200595,RMVar_hsa_circ_18859,RMVar_hsa_circ_200593,RMVar_hsa_circ_200600,RMVar_hsa_circ_297031 45337 RMVar_ID_45337 Human_SNP_ID_74629344 A-to-I Human chr2 - 61528569 61528569 61528569 TCCTGATTCTTGGGGAATCTTGGCTCACTGCAACCTCCGCTCCTGGATTCAAGCGATTCTCCTGC TCCTGATTCTTGGGGAATCTTGGCTCACTGCAGCCTCCGCTCCTGGATTCAAGCGATTCTCCTGC T C XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs376664602 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6937023,Human_RBP_ID_13933171 RMVar_hsa_circ_315608,RMVar_hsa_circ_200502,RMVar_hsa_circ_302279,RMVar_hsa_circ_200514,RMVar_hsa_circ_296615,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_302621,RMVar_hsa_circ_316390,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_200543,RMVar_hsa_circ_308693,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_333365,RMVar_hsa_circ_200568,RMVar_hsa_circ_304877,RMVar_hsa_circ_200569,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_289892,RMVar_hsa_circ_98453,RMVar_hsa_circ_200581,RMVar_hsa_circ_326823,RMVar_hsa_circ_301783,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590,RMVar_hsa_circ_278039,RMVar_hsa_circ_200594,RMVar_hsa_circ_200595,RMVar_hsa_circ_18859,RMVar_hsa_circ_200593,RMVar_hsa_circ_200600,RMVar_hsa_circ_297031 45338 RMVar_ID_45338 Human_SNP_ID_74629733 A-to-I Human chr2 - 61529508 61529508 61529508 GGGATTACAAGTACGCCCCACCATGCCCAGCTAATTTTTGAATTTTTAGTAGAGACGGGGTTTCA GGGATTACAAGTACGCCCCACCATGCCCAGCTTATTTTTGAATTTTTAGTAGAGACGGGGTTTCA T A XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1036514112 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_315608,RMVar_hsa_circ_200502,RMVar_hsa_circ_302279,RMVar_hsa_circ_200514,RMVar_hsa_circ_296615,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_302621,RMVar_hsa_circ_316390,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_200543,RMVar_hsa_circ_308693,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_333365,RMVar_hsa_circ_200568,RMVar_hsa_circ_304877,RMVar_hsa_circ_200569,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_289892,RMVar_hsa_circ_98453,RMVar_hsa_circ_200581,RMVar_hsa_circ_326823,RMVar_hsa_circ_301783,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590,RMVar_hsa_circ_278039,RMVar_hsa_circ_200594,RMVar_hsa_circ_200595,RMVar_hsa_circ_18859,RMVar_hsa_circ_200593,RMVar_hsa_circ_200600,RMVar_hsa_circ_297031 45339 RMVar_ID_45339 Human_SNP_ID_74629734 A-to-I Human chr2 - 61529508 61529508 61529508 GGGATTACAAGTACGCCCCACCATGCCCAGCTAATTTTTGAATTTTTAGTAGAGACGGGGTTTCA GGGATTACAAGTACGCCCCACCATGCCCAGCTGATTTTTGAATTTTTAGTAGAGACGGGGTTTCA T C XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1036514112 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_315608,RMVar_hsa_circ_200502,RMVar_hsa_circ_302279,RMVar_hsa_circ_200514,RMVar_hsa_circ_296615,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_302621,RMVar_hsa_circ_316390,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_200543,RMVar_hsa_circ_308693,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_333365,RMVar_hsa_circ_200568,RMVar_hsa_circ_304877,RMVar_hsa_circ_200569,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_289892,RMVar_hsa_circ_98453,RMVar_hsa_circ_200581,RMVar_hsa_circ_326823,RMVar_hsa_circ_301783,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590,RMVar_hsa_circ_278039,RMVar_hsa_circ_200594,RMVar_hsa_circ_200595,RMVar_hsa_circ_18859,RMVar_hsa_circ_200593,RMVar_hsa_circ_200600,RMVar_hsa_circ_297031 45340 RMVar_ID_45340 Human_SNP_ID_74629742 A-to-I Human chr2 - 61529543 61529543 61529543 CAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAACTGGGATTACAAGTACGCCCCACCATGCCCAG CAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAAGTACGCCCCACCATGCCCAG T C XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167054823 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_315608,RMVar_hsa_circ_200502,RMVar_hsa_circ_302279,RMVar_hsa_circ_200514,RMVar_hsa_circ_296615,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_302621,RMVar_hsa_circ_316390,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_200543,RMVar_hsa_circ_308693,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_333365,RMVar_hsa_circ_200568,RMVar_hsa_circ_304877,RMVar_hsa_circ_200569,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_289892,RMVar_hsa_circ_98453,RMVar_hsa_circ_200581,RMVar_hsa_circ_326823,RMVar_hsa_circ_301783,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590,RMVar_hsa_circ_278039,RMVar_hsa_circ_200594,RMVar_hsa_circ_200595,RMVar_hsa_circ_18859,RMVar_hsa_circ_200593,RMVar_hsa_circ_200600,RMVar_hsa_circ_297031 45341 RMVar_ID_45341 Human_SNP_ID_74630761 A-to-I Human chr2 - 61532711 61532711 61532711 CACCTGCCTTAGCCTCCCGAGTAGCTGGGACTACAGACGCGCCACCATGCCCAGCTAATTTTTTG CACCTGCCTTAGCCTCCCGAGTAGCTGGGACTCCAGACGCGCCACCATGCCCAGCTAATTTTTTG T G XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1000329001 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_315608,RMVar_hsa_circ_200502,RMVar_hsa_circ_302279,RMVar_hsa_circ_200514,RMVar_hsa_circ_296615,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_302621,RMVar_hsa_circ_316390,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_200543,RMVar_hsa_circ_308693,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_333365,RMVar_hsa_circ_200568,RMVar_hsa_circ_304877,RMVar_hsa_circ_200569,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_289892,RMVar_hsa_circ_98453,RMVar_hsa_circ_200581,RMVar_hsa_circ_326823,RMVar_hsa_circ_301783,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590,RMVar_hsa_circ_278039,RMVar_hsa_circ_200594,RMVar_hsa_circ_200595,RMVar_hsa_circ_18859,RMVar_hsa_circ_200593,RMVar_hsa_circ_200600,RMVar_hsa_circ_297031 45342 RMVar_ID_45342 Human_SNP_ID_74631061 A-to-I Human chr2 - 61533778 61533778 61533778 AATGTGGTGAATTGCTTATACCATGGAGAAGGAGCCCAGGTAAAGTAGCCAACCAAAACTTTATA AATGTGGTGAATTGCTTATACCATGGAGAAGGTGCCCAGGTAAAGTAGCCAACCAAAACTTTATA T A XPO1 Ensembl:ENSG00000082898 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs746740414 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_242293,Human_RBP_ID_922143,Human_RBP_ID_1023721,Human_RBP_ID_1588610,Human_RBP_ID_1921251,Human_RBP_ID_2655928,Human_RBP_ID_3630517,Human_RBP_ID_6937128,Human_RBP_ID_8522634,Human_RBP_ID_8849288,Human_RBP_ID_9109434,Human_RBP_ID_9383887,Human_RBP_ID_13933448,Human_RBP_ID_17191973,Human_RBP_ID_17959247,Human_RBP_ID_18763484,Human_RBP_ID_19100414,Human_RBP_ID_26786946 Human_Splice_Rec_251461,Human_Splice_Rec_251507,Human_Splice_Rec_251577,Human_Splice_Rec_251625,Human_Splice_Rec_251703,Human_Splice_Rec_251717,Human_Splice_Rec_251733,Human_Splice_Rec_251739,Human_Splice_Rec_251747,Human_Splice_Rec_251753,Human_Splice_Rec_251755,Human_Splice_Rec_251759,Human_Splice_Rec_251763 Human_miRNA_ID_2552580,Human_miRNA_ID_2552581 RMVar_hsa_circ_315608,RMVar_hsa_circ_200502,RMVar_hsa_circ_302279,RMVar_hsa_circ_200514,RMVar_hsa_circ_296615,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_302621,RMVar_hsa_circ_316390,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_200543,RMVar_hsa_circ_308693,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_333365,RMVar_hsa_circ_200568,RMVar_hsa_circ_304877,RMVar_hsa_circ_200569,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_289892,RMVar_hsa_circ_98453,RMVar_hsa_circ_200581,RMVar_hsa_circ_326823,RMVar_hsa_circ_301783,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590,RMVar_hsa_circ_278039,RMVar_hsa_circ_200594,RMVar_hsa_circ_200595,RMVar_hsa_circ_18859,RMVar_hsa_circ_200593,RMVar_hsa_circ_200601,RMVar_hsa_circ_200600,RMVar_hsa_circ_297031,RMVar_hsa_circ_370468 45343 RMVar_ID_45343 Human_SNP_ID_74711666 A-to-I Human chr2 - 61833812 61833812 61833812 TGGCCCAGGCTGGTCGTGAACTCCTGGCCTCAAGTGATCCTCCCACCTCCACCTCCCAAGTTGAT TGGCCCAGGCTGGTCGTGAACTCCTGGCCTCAGGTGATCCTCCCACCTCCACCTCCCAAGTTGAT T C FAM161A Ensembl:ENSG00000170264 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934206907 Functional Loss SNV dbSNP153 33..33 33 - - - 45344 RMVar_ID_45344 Human_SNP_ID_74711864 A-to-I Human chr2 - 61834591 61834591 61834591 GGGCATGGTTTTGCGTGCCTGTAGTCCCAACTACTTGGGAGGCTGAGGCAGGAGAATTGCTTGAA GGGCATGGTTTTGCGTGCCTGTAGTCCCAACTGCTTGGGAGGCTGAGGCAGGAGAATTGCTTGAA T C FAM161A Ensembl:ENSG00000170264 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs949043399 Functional Loss SNV dbSNP153 33..33 33 - - - 45345 RMVar_ID_45345 Human_SNP_ID_74711865 A-to-I Human chr2 - 61834591 61834591 61834591 GGGCATGGTTTTGCGTGCCTGTAGTCCCAACTACTTGGGAGGCTGAGGCAGGAGAATTGCTTGAA GGGCATGGTTTTGCGTGCCTGTAGTCCCAACTCCTTGGGAGGCTGAGGCAGGAGAATTGCTTGAA T G FAM161A Ensembl:ENSG00000170264 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs949043399 Functional Loss SNV dbSNP153 33..33 33 - - - 45346 RMVar_ID_45346 Human_SNP_ID_74711869 A-to-I Human chr2 - 61834601 61834601 61834601 AAAATTAGCCGGGCATGGTTTTGCGTGCCTGTAGTCCCAACTACTTGGGAGGCTGAGGCAGGAGA AAAATTAGCCGGGCATGGTTTTGCGTGCCTGTGGTCCCAACTACTTGGGAGGCTGAGGCAGGAGA T C FAM161A Ensembl:ENSG00000170264 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1206368487 Functional Loss SNV dbSNP153 33..33 33 - - - 45347 RMVar_ID_45347 Human_SNP_ID_74712405 A-to-I Human chr2 - 61836728 61836728 61836728 TCTCTACTAAAAATACAGAAAATTAGCCAGGCATGGTGGTGCACACCTGTAATCTCAGCTATTCG TCTCTACTAAAAATACAGAAAATTAGCCAGGCTTGGTGGTGCACACCTGTAATCTCAGCTATTCG T A FAM161A Ensembl:ENSG00000170264 Protein coding intron GSE47997;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 23474544,31158229,31158229 RNA-Seq:(High) rs1481646649 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49202,RMVar_hsa_circ_327138 45348 RMVar_ID_45348 Human_SNP_ID_74712408 A-to-I Human chr2 - 61836732 61836732 61836732 CTCATCTCTACTAAAAATACAGAAAATTAGCCAGGCATGGTGGTGCACACCTGTAATCTCAGCTA CTCATCTCTACTAAAAATACAGAAAATTAGCCGGGCATGGTGGTGCACACCTGTAATCTCAGCTA T C FAM161A Ensembl:ENSG00000170264 Protein coding intron GSE47997;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1229740918 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49202,RMVar_hsa_circ_327138 45349 RMVar_ID_45349 Human_SNP_ID_74712412 A-to-I Human chr2 - 61836739 61836738 61836739 TGAAACCCTCATCTCTACTAAAAATACAGAAAATTAGCCAGGCATGGTGGTGCACACCTGTAATC TGAAACCCTCATCTCTACTAAAAATACAGAAA_TTAGCCAGGCATGGTGGTGCACACCTGTAATC AT A FAM161A Ensembl:ENSG00000170264 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1310596735 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_49202,RMVar_hsa_circ_327138 45350 RMVar_ID_45350 Human_SNP_ID_74712431 A-to-I Human chr2 - 61836793 61836793 61836793 AAGACAGGCAGATCACCTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCCTCA AAGACAGGCAGATCACCTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCTCA T C FAM161A Ensembl:ENSG00000170264 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1226840554 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25556645 Human_Splice_Rec_251796 RMVar_hsa_circ_49202,RMVar_hsa_circ_327138 45351 RMVar_ID_45351 Human_SNP_ID_74712439 A-to-I Human chr2 - 61836820 61836820 61836820 CCTGTAATCCCAGCACTTTGAGAGGCCAAGACAGGCAGATCACCTGAGGTCAGGAGTTCAAGACC CCTGTAATCCCAGCACTTTGAGAGGCCAAGACCGGCAGATCACCTGAGGTCAGGAGTTCAAGACC T G FAM161A Ensembl:ENSG00000170264 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1440325727 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_147523 Human_Splice_Rec_251796 RMVar_hsa_circ_49202,RMVar_hsa_circ_327138 45352 RMVar_ID_45352 Human_SNP_ID_74712442 A-to-I Human chr2 - 61836825 61836825 61836825 TCATGCCTGTAATCCCAGCACTTTGAGAGGCCAAGACAGGCAGATCACCTGAGGTCAGGAGTTCA TCATGCCTGTAATCCCAGCACTTTGAGAGGCCGAGACAGGCAGATCACCTGAGGTCAGGAGTTCA T C FAM161A Ensembl:ENSG00000170264 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1462458075 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_251796 RMVar_hsa_circ_49202,RMVar_hsa_circ_327138 45353 RMVar_ID_45353 Human_SNP_ID_74712489 A-to-I Human chr2 - 61836982 61836982 61836982 CATGCCCCTGTAGTTCCACCTACTCGAGAGCTAAGGTGGGAGGATCATTTGAGCCCAGGAAGTCA CATGCCCCTGTAGTTCCACCTACTCGAGAGCTGAGGTGGGAGGATCATTTGAGCCCAGGAAGTCA T C FAM161A Ensembl:ENSG00000170264 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1042565704 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49202,RMVar_hsa_circ_327138 45354 RMVar_ID_45354 Human_SNP_ID_74712511 A-to-I Human chr2 - 61837049 61837048 61837049 AGCCTGGTAAACATAATGAGACCCCCATCTCTACAAAAAATTTAAAAAAATTAGCCAGGTGTGGT AGCCTGGTAAACATAATGAGACCCCCATCTCT_CAAAAAATTTAAAAAAATTAGCCAGGTGTGGT GT G FAM161A Ensembl:ENSG00000170264 Protein coding intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1014788675 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_49202,RMVar_hsa_circ_327138 45355 RMVar_ID_45355 Human_SNP_ID_74712532 A-to-I Human chr2 - 61837134 61837134 61837134 GCTGGATGCCATGGCTCACATCTGTAATCCCAACACCTCAGGAGTACAAGGCAGGAAGATTGCTT GCTGGATGCCATGGCTCACATCTGTAATCCCAGCACCTCAGGAGTACAAGGCAGGAAGATTGCTT T C FAM161A Ensembl:ENSG00000170264 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1446923587 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49202,RMVar_hsa_circ_327138 45356 RMVar_ID_45356 Human_SNP_ID_74722363 A-to-I Human chr2 - 61870261 61870257 61870261 TGTTTTGTTTTGTTTTTTTGAGACAGAGTCTCACTCTGTTACCCAGGCTGGAGTGCAGTGGCACA TGTTTTGTTTTGTTTTTTTGAGACAGAGTCTC____TGTTACCCAGGCTGGAGTGCAGTGGCACA AGAGT A CCT4 Ensembl:ENSG00000115484 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1389839678 Functional Loss DEL dbSNP153 33..36 33 - - - 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 45357 RMVar_ID_45357 Human_SNP_ID_74722492 A-to-I Human chr2 - 61870668 61870668 61870668 GCAATTCACCTGCCTCAGCCTTCCAAAGTGCTAGGATTATAGGCGTGAGCCACGGTGCGGGGCCT GCAATTCACCTGCCTCAGCCTTCCAAAGTGCTTGGATTATAGGCGTGAGCCACGGTGCGGGGCCT T A CCT4 Ensembl:ENSG00000115484 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1360312238 Functional Loss SNV dbSNP153 33..33 33 - - - 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 45358 RMVar_ID_45358 Human_SNP_ID_74722518 A-to-I Human chr2 - 61870753 61870753 61870753 CAGGCCGGGCTAATTTTTTTGTATTTTTTAGTAGATATGGTGTTTCACTGTGTTGCTGAGGCTGG CAGGCCGGGCTAATTTTTTTGTATTTTTTAGTTGATATGGTGTTTCACTGTGTTGCTGAGGCTGG T A CCT4 Ensembl:ENSG00000115484 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1490802959 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13934248 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 45359 RMVar_ID_45359 Human_SNP_ID_74722532 A-to-I Human chr2 - 61870800 61870800 61870800 ATTCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCGCCCACCACCAGGCCGGGCTAATTTTT ATTCTGCCTCAGCCTCCTGAGTAGCTGGGACTGCAGGCGCCCACCACCAGGCCGGGCTAATTTTT T C CCT4 Ensembl:ENSG00000115484 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs983399101 Functional Loss SNV dbSNP153 33..33 33 - - - 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 45360 RMVar_ID_45360 Human_SNP_ID_74722553 A-to-I Human chr2 - 61870857 61870857 61870857 GCTGCAGTGCAGTAGCACTGTCAGCTCACTGCAACCTCCTCCTCCCAAGTTCAAGCAATTCTGCC GCTGCAGTGCAGTAGCACTGTCAGCTCACTGCGACCTCCTCCTCCCAAGTTCAAGCAATTCTGCC T C CCT4 Ensembl:ENSG00000115484 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1382128737 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13934249 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 45361 RMVar_ID_45361 Human_SNP_ID_74722569 A-to-I Human chr2 - 61870908 61870908 61870908 GTTTGTTTGTTTGTTTTTTCTTTGGAGACGGAATCTTGCTCTGTTGCCCAGGCTGCAGTGCAGTA GTTTGTTTGTTTGTTTTTTCTTTGGAGACGGACTCTTGCTCTGTTGCCCAGGCTGCAGTGCAGTA T G CCT4 Ensembl:ENSG00000115484 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs896759478 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13934251,Human_RBP_ID_23879263 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 45362 RMVar_ID_45362 Human_SNP_ID_74726136 A-to-I Human chr2 - 61882071 61882071 61882071 AAAATCAGCTGGGCGTGGTGGTGCATGCCTTTAATTTCAGCTACTCGGAGGCAGAGACAGGAGAA AAAATCAGCTGGGCGTGGTGGTGCATGCCTTTGATTTCAGCTACTCGGAGGCAGAGACAGGAGAA T C CCT4 Ensembl:ENSG00000115484 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1305899301 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13934546 RMVar_hsa_circ_200616,RMVar_hsa_circ_333000,RMVar_hsa_circ_72743,RMVar_hsa_circ_200607,RMVar_hsa_circ_73668,RMVar_hsa_circ_332577,RMVar_hsa_circ_288297,RMVar_hsa_circ_200608,RMVar_hsa_circ_279828,RMVar_hsa_circ_273915,RMVar_hsa_circ_200617,RMVar_hsa_circ_200620,RMVar_hsa_circ_274755,RMVar_hsa_circ_323082,RMVar_hsa_circ_365896,RMVar_hsa_circ_200621,RMVar_hsa_circ_369607,RMVar_hsa_circ_200623,RMVar_hsa_circ_332282,RMVar_hsa_circ_346463 45363 RMVar_ID_45363 Human_SNP_ID_74726327 A-to-I Human chr2 - 61882637 61882637 61882637 TGGGTGTGTGGTGCGCACCTGTGGTCTCAGCTACTCAGGAGGCTGAGGTGGGAGAATTGTTTGAG TGGGTGTGTGGTGCGCACCTGTGGTCTCAGCTGCTCAGGAGGCTGAGGTGGGAGAATTGTTTGAG T C CCT4 Ensembl:ENSG00000115484 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1416435992 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_200616,RMVar_hsa_circ_333000,RMVar_hsa_circ_72743,RMVar_hsa_circ_200607,RMVar_hsa_circ_73668,RMVar_hsa_circ_332577,RMVar_hsa_circ_288297,RMVar_hsa_circ_200608,RMVar_hsa_circ_279828,RMVar_hsa_circ_273915,RMVar_hsa_circ_200617,RMVar_hsa_circ_200620,RMVar_hsa_circ_274755,RMVar_hsa_circ_323082,RMVar_hsa_circ_365896,RMVar_hsa_circ_200621,RMVar_hsa_circ_369607,RMVar_hsa_circ_200623,RMVar_hsa_circ_332282,RMVar_hsa_circ_346463 45364 RMVar_ID_45364 Human_SNP_ID_74726545 A-to-I Human chr2 - 61883365 61883365 61883365 TCATCCAGGCTAGAGTGCCGTGGCACAATCTCAGCTCACTGCAACCTCTGCCTCCCAGATTCATT TCATCCAGGCTAGAGTGCCGTGGCACAATCTCGGCTCACTGCAACCTCTGCCTCCCAGATTCATT T C CCT4 Ensembl:ENSG00000115484 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1185020720 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5381045 RMVar_hsa_circ_200616,RMVar_hsa_circ_333000,RMVar_hsa_circ_72743,RMVar_hsa_circ_200607,RMVar_hsa_circ_73668,RMVar_hsa_circ_332577,RMVar_hsa_circ_288297,RMVar_hsa_circ_200608,RMVar_hsa_circ_279828,RMVar_hsa_circ_273915,RMVar_hsa_circ_200617,RMVar_hsa_circ_200620,RMVar_hsa_circ_274755,RMVar_hsa_circ_323082,RMVar_hsa_circ_365896,RMVar_hsa_circ_200621,RMVar_hsa_circ_369607,RMVar_hsa_circ_200623,RMVar_hsa_circ_332282,RMVar_hsa_circ_346463 45365 RMVar_ID_45365 Human_SNP_ID_74726546 A-to-I Human chr2 - 61883370 61883370 61883370 CTCTGTCATCCAGGCTAGAGTGCCGTGGCACAATCTCAGCTCACTGCAACCTCTGCCTCCCAGAT CTCTGTCATCCAGGCTAGAGTGCCGTGGCACAGTCTCAGCTCACTGCAACCTCTGCCTCCCAGAT T C CCT4 Ensembl:ENSG00000115484 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs544767936 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5381045 RMVar_hsa_circ_200616,RMVar_hsa_circ_333000,RMVar_hsa_circ_72743,RMVar_hsa_circ_200607,RMVar_hsa_circ_73668,RMVar_hsa_circ_332577,RMVar_hsa_circ_288297,RMVar_hsa_circ_200608,RMVar_hsa_circ_279828,RMVar_hsa_circ_273915,RMVar_hsa_circ_200617,RMVar_hsa_circ_200620,RMVar_hsa_circ_274755,RMVar_hsa_circ_323082,RMVar_hsa_circ_365896,RMVar_hsa_circ_200621,RMVar_hsa_circ_369607,RMVar_hsa_circ_200623,RMVar_hsa_circ_332282,RMVar_hsa_circ_346463 45366 RMVar_ID_45366 Human_SNP_ID_74727585 A-to-I Human chr2 - 61886245 61886245 61886245 CACCGCCACACCCGGCTCATTTTTGTATTAGTAGAGGCAGGGTTTCGCCATGTTGTCCAGGCTGG CACCGCCACACCCGGCTCATTTTTGTATTAGTGGAGGCAGGGTTTCGCCATGTTGTCCAGGCTGG T C CCT4 Ensembl:ENSG00000115484 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1349472492 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13934637,Human_RBP_ID_25556916 RMVar_hsa_circ_200625 45367 RMVar_ID_45367 Human_SNP_ID_74727605 A-to-I Human chr2 - 61886286 61886286 61886286 TGCCTCAGCCTCCCGAGTAGCTAGCTGGGACTACAGATGCGCACCGCCACACCCGGCTCATTTTT TGCCTCAGCCTCCCGAGTAGCTAGCTGGGACTTCAGATGCGCACCGCCACACCCGGCTCATTTTT T A CCT4 Ensembl:ENSG00000115484 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1558509292 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_200625 45368 RMVar_ID_45368 Human_SNP_ID_74733689 A-to-I Human chr2 + 61907768 61907768 61907768 GCTGGAGTGCAATGGTGTGATCTCCGCTCTCTACAACCTCCGCCTCCCGGGTTCAGGTGATTCTC GCTGGAGTGCAATGGTGTGATCTCCGCTCTCTGCAACCTCCGCCTCCCGGGTTCAGGTGATTCTC A G COMMD1 Ensembl:ENSG00000173163 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559816459 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120995,RMVar_hsa_circ_200626 45369 RMVar_ID_45369 Human_SNP_ID_74735453 A-to-I Human chr2 + 61914357 61914357 61914357 AAATTAAAAATGACCTCTAGCCTGGCCAGCATAGTGAAACCTTGTCTCTACTAAAAATACAAAAA AAATTAAAAATGACCTCTAGCCTGGCCAGCATGGTGAAACCTTGTCTCTACTAAAAATACAAAAA A G COMMD1 Ensembl:ENSG00000173163 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1188842475 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120995,RMVar_hsa_circ_200626 45370 RMVar_ID_45370 Human_SNP_ID_74739335 A-to-I Human chr2 + 61929777 61929776 61929777 AACATAATGAGACCTGGTCTTTACAAAAAATTAGTTGGGTATGGTGGTGCATGTCTGTAGTCCCA AACATAATGAGACCTGGTCTTTACAAAAAATT_GTTGGGTATGGTGGTGCATGTCTGTAGTCCCA TA T COMMD1 Ensembl:ENSG00000173163 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1207763826 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_120995,RMVar_hsa_circ_200626 45371 RMVar_ID_45371 Human_SNP_ID_74739336 A-to-I Human chr2 + 61929777 61929777 61929777 AACATAATGAGACCTGGTCTTTACAAAAAATTAGTTGGGTATGGTGGTGCATGTCTGTAGTCCCA AACATAATGAGACCTGGTCTTTACAAAAAATTGGTTGGGTATGGTGGTGCATGTCTGTAGTCCCA A G COMMD1 Ensembl:ENSG00000173163 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1440850522 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120995,RMVar_hsa_circ_200626 45372 RMVar_ID_45372 Human_SNP_ID_74749445 A-to-I Human chr2 + 61970023 61970023 61970023 TCACACCTGTAATCCCAGCACTCTGGGAGGCCAAGGTAGGTGGATCACCTGAGGTCAGGAGTTCG TCACACCTGTAATCCCAGCACTCTGGGAGGCCCAGGTAGGTGGATCACCTGAGGTCAGGAGTTCG A C COMMD1 Ensembl:ENSG00000173163 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs551422397 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120995,RMVar_hsa_circ_200626 45373 RMVar_ID_45373 Human_SNP_ID_74749450 A-to-I Human chr2 + 61970047 61970047 61970047 GGGAGGCCAAGGTAGGTGGATCACCTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAATATGATGA GGGAGGCCAAGGTAGGTGGATCACCTGAGGTCGGGAGTTCGAGACCAGCCTGGCCAATATGATGA A G COMMD1 Ensembl:ENSG00000173163 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs745654715 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120995,RMVar_hsa_circ_200626 45374 RMVar_ID_45374 Human_SNP_ID_74749714 A-to-I Human chr2 + 61971026 61971026 61971026 TGTCTCCTGGGCTCAAGCAATCCTTCCACCTCAGCCTCCGGAGTAGCTGGGACTACAAGCATGTG TGTCTCCTGGGCTCAAGCAATCCTTCCACCTCTGCCTCCGGAGTAGCTGGGACTACAAGCATGTG A T COMMD1 Ensembl:ENSG00000173163 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968554672 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120995,RMVar_hsa_circ_200626 45375 RMVar_ID_45375 Human_SNP_ID_74749875 A-to-I Human chr2 + 61971638 61971638 61971638 AAGCCTCATGATATCCCACAGTTGTCCAGGCTAGTCTTGAACTCCTGGGCTCAAGTGATCCTTTT AAGCCTCATGATATCCCACAGTTGTCCAGGCTGGTCTTGAACTCCTGGGCTCAAGTGATCCTTTT A G COMMD1 Ensembl:ENSG00000173163 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1438944259 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120995,RMVar_hsa_circ_200626 45376 RMVar_ID_45376 Human_SNP_ID_74763234 A-to-I Human chr2 + 62023501 62023501 62023501 TGCAAATATTTACTGTGGATTTTTTTTTTTTTAATACAGAATTTCTCTCTTGTCACCCAGGCTGG TGCAAATATTTACTGTGGATTTTTTTTTTTTTGATACAGAATTTCTCTCTTGTCACCCAGGCTGG A G COMMD1 Ensembl:ENSG00000173163 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1156343775 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113286,RMVar_hsa_circ_120995,RMVar_hsa_circ_200626,RMVar_hsa_circ_200628 45377 RMVar_ID_45377 Human_SNP_ID_74763791 A-to-I Human chr2 + 62025894 62025894 62025894 TTTTATAGTTTTGATAGAGGTGGGGTTTCGCCATGTTGGCCAGCCTGGTCTCAAACTCCTGGCCT TTTTATAGTTTTGATAGAGGTGGGGTTTCGCCGTGTTGGCCAGCCTGGTCTCAAACTCCTGGCCT A G COMMD1 Ensembl:ENSG00000173163 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1420236748 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113286,RMVar_hsa_circ_120995,RMVar_hsa_circ_200626,RMVar_hsa_circ_200628 45378 RMVar_ID_45378 Human_SNP_ID_74765381 A-to-I Human chr2 + 62032870 62032870 62032870 TTGGCTCACTGCATCCTCCACCCTCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGC TTGGCTCACTGCATCCTCCACCCTCCAGGTTCGAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGC A G COMMD1 Ensembl:ENSG00000173163 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs762105342 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113286,RMVar_hsa_circ_120995,RMVar_hsa_circ_200626,RMVar_hsa_circ_200628 45379 RMVar_ID_45379 Human_SNP_ID_74794696 A-to-I Human chr2 + 62153909 62153909 62153909 TCCCAGCTGAGGCAGGAGAATCACTTGAACTCAGGAGGCGGATGTTGTGGTGAGCTGAGATTGCG TCCCAGCTGAGGCAGGAGAATCACTTGAACTCGGGAGGCGGATGTTGTGGTGAGCTGAGATTGCG A G lnc-COMMD1-3 RNACentral:URS00008B6D74 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs888287936 Functional Loss SNV dbSNP153 33..33 33 - - - 45380 RMVar_ID_45380 Human_SNP_ID_74984919 A-to-I Human chr2 + 62912312 62912312 62912312 TGTGGCTCACACCTGTAATCCCAGCACTTTGGAAGGCTGAGGCGGGCAGATCACTTGAGGTAAGG TGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGCAGATCACTTGAGGTAAGG A G EHBP1 Ensembl:ENSG00000115504 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1442808599 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1002,RMVar_hsa_circ_200631,RMVar_hsa_circ_102104,RMVar_hsa_circ_62128,RMVar_hsa_circ_5814,RMVar_hsa_circ_64389,RMVar_hsa_circ_52547,RMVar_hsa_circ_17344,RMVar_hsa_circ_52857,RMVar_hsa_circ_57648,RMVar_hsa_circ_200640,RMVar_hsa_circ_100068,RMVar_hsa_circ_200639,RMVar_hsa_circ_200641,RMVar_hsa_circ_19190 45381 RMVar_ID_45381 Human_SNP_ID_74984925 A-to-I Human chr2 + 62912332 62912332 62912332 CCAGCACTTTGGAAGGCTGAGGCGGGCAGATCACTTGAGGTAAGGAGTTTGAGACCAGCATGACC CCAGCACTTTGGAAGGCTGAGGCGGGCAGATCTCTTGAGGTAAGGAGTTTGAGACCAGCATGACC A T EHBP1 Ensembl:ENSG00000115504 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1174999123 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1002,RMVar_hsa_circ_200631,RMVar_hsa_circ_102104,RMVar_hsa_circ_62128,RMVar_hsa_circ_5814,RMVar_hsa_circ_64389,RMVar_hsa_circ_52547,RMVar_hsa_circ_17344,RMVar_hsa_circ_52857,RMVar_hsa_circ_57648,RMVar_hsa_circ_200640,RMVar_hsa_circ_100068,RMVar_hsa_circ_200639,RMVar_hsa_circ_200641,RMVar_hsa_circ_19190 45382 RMVar_ID_45382 Human_SNP_ID_75040620 A-to-I Human chr2 - 63149857 63149857 63149857 AGCTAGAATTATAGGTGCATGCCACCATGCCTAGCTAATTTTGGGCTTTTTGTAGAGACAGGGTC AGCTAGAATTATAGGTGCATGCCACCATGCCTGGCTAATTTTGGGCTTTTTGTAGAGACAGGGTC T C WDPCP Ensembl:ENSG00000143951 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560907118 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_200658 45383 RMVar_ID_45383 Human_SNP_ID_75062096 A-to-I Human chr2 - 63243378 63243377 63243378 TGTGAGAAAATTAAATAAATCACAAGAAAAAAATAACCCAATTAAAAGTGGGCAAAGGACATGAA TGTGAGAAAATTAAATAAATCACAAGAAAAAA_TAACCCAATTAAAAGTGGGCAAAGGACATGAA AT A WDPCP Ensembl:ENSG00000143951 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1373855893 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_4757,RMVar_hsa_circ_113626,RMVar_hsa_circ_362750,RMVar_hsa_circ_306096,RMVar_hsa_circ_112479,RMVar_hsa_circ_200661,RMVar_hsa_circ_200662,RMVar_hsa_circ_200663 45384 RMVar_ID_45384 Human_SNP_ID_75108110 A-to-I Human chr2 - 63442445 63442445 63442445 GGCAAGAGCATGCATACATTGGTTAGATAACTAATCTATGCCTGGAGGCAGGAGCAGTGATTTGG GGCAAGAGCATGCATACATTGGTTAGATAACTCATCTATGCCTGGAGGCAGGAGCAGTGATTTGG T G WDPCP Ensembl:ENSG00000143951 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1356265638 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_362750,RMVar_hsa_circ_306096,RMVar_hsa_circ_76365,RMVar_hsa_circ_337203,RMVar_hsa_circ_42139,RMVar_hsa_circ_326095,RMVar_hsa_circ_296656,RMVar_hsa_circ_52297,RMVar_hsa_circ_48735,RMVar_hsa_circ_339099,RMVar_hsa_circ_55610,RMVar_hsa_circ_269900,RMVar_hsa_circ_48631,RMVar_hsa_circ_310169,RMVar_hsa_circ_334268,RMVar_hsa_circ_276193,RMVar_hsa_circ_317728,RMVar_hsa_circ_273191,RMVar_hsa_circ_9207,RMVar_hsa_circ_200669,RMVar_hsa_circ_200671,RMVar_hsa_circ_200670,RMVar_hsa_circ_200667,RMVar_hsa_circ_200668,RMVar_hsa_circ_200666,RMVar_hsa_circ_325884 45385 RMVar_ID_45385 Human_SNP_ID_75108256 A-to-I Human chr2 - 63442990 63442990 63442990 CAAATCACTGCTCCTGCCTCCATGCATAGATCAGTTATCTAACCAGTGTATGCATGCTTTTGGCT CAAATCACTGCTCCTGCCTCCATGCATAGATCGGTTATCTAACCAGTGTATGCATGCTTTTGGCT T C WDPCP Ensembl:ENSG00000143951 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1330172213 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_362750,RMVar_hsa_circ_306096,RMVar_hsa_circ_76365,RMVar_hsa_circ_337203,RMVar_hsa_circ_42139,RMVar_hsa_circ_326095,RMVar_hsa_circ_296656,RMVar_hsa_circ_52297,RMVar_hsa_circ_48735,RMVar_hsa_circ_339099,RMVar_hsa_circ_55610,RMVar_hsa_circ_269900,RMVar_hsa_circ_48631,RMVar_hsa_circ_310169,RMVar_hsa_circ_334268,RMVar_hsa_circ_276193,RMVar_hsa_circ_317728,RMVar_hsa_circ_273191,RMVar_hsa_circ_9207,RMVar_hsa_circ_200669,RMVar_hsa_circ_200671,RMVar_hsa_circ_200670,RMVar_hsa_circ_200667,RMVar_hsa_circ_200668,RMVar_hsa_circ_200666,RMVar_hsa_circ_325884 45386 RMVar_ID_45386 Human_SNP_ID_75121519 A-to-I Human chr2 - 63501372 63501372 63501372 TTTTGTAGAGACAGGGTCTGACTATGTTGCCCAGGCTGATCTTGAACTCCTGACTTAGAGCAATC TTTTGTAGAGACAGGGTCTGACTATGTTGCCCGGGCTGATCTTGAACTCCTGACTTAGAGCAATC T C WDPCP Ensembl:ENSG00000143951 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs557125987 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42139,RMVar_hsa_circ_296656,RMVar_hsa_circ_269900,RMVar_hsa_circ_48631,RMVar_hsa_circ_334268,RMVar_hsa_circ_273191,RMVar_hsa_circ_200666,RMVar_hsa_circ_325884,RMVar_hsa_circ_200680,RMVar_hsa_circ_279788,RMVar_hsa_circ_111548,RMVar_hsa_circ_200682 45387 RMVar_ID_45387 Human_SNP_ID_75165341 A-to-I Human chr2 - 63684675 63684675 63684675 GCAGCTTCTGGAAGAACCACTTGTTCTTGCCTATCTTGTATCTCTCTTCAAACTTGACCTTGACC GCAGCTTCTGGAAGAACCACTTGTTCTTGCCTGTCTTGTATCTCTCTTCAAACTTGACCTTGACC T C WDPCP Ensembl:ENSG00000143951 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs556462778 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_305664 45388 RMVar_ID_45388 Human_SNP_ID_75205520 A-to-I Human chr2 + 63857190 63857190 63857190 AGGCATGGTGGTATGCGCCTGTGGTCCCAGCTACTGGGGAGGCTGAGGTGGGAGGGTAGTTTAAG AGGCATGGTGGTATGCGCCTGTGGTCCCAGCTGCTGGGGAGGCTGAGGTGGGAGGGTAGTTTAAG A G UGP2 Ensembl:ENSG00000169764 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1558939116 Functional Loss SNV dbSNP153 33..33 33 - - - 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_324287,RMVar_hsa_circ_272648,RMVar_hsa_circ_270110,RMVar_hsa_circ_200702,RMVar_hsa_circ_200703,RMVar_hsa_circ_200699,RMVar_hsa_circ_200700 45389 RMVar_ID_45389 Human_SNP_ID_75205652 A-to-I Human chr2 + 63857567 63857567 63857567 GTATTTTTTTTGTAGACACCGGGTTTTGCCATATTGCCGAGGCTGGTCTCAAACTCCTGAGCTCA GTATTTTTTTTGTAGACACCGGGTTTTGCCATGTTGCCGAGGCTGGTCTCAAACTCCTGAGCTCA A G UGP2 Ensembl:ENSG00000169764 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1420087366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_253106,Human_Splice_Rec_253182,Human_Splice_Rec_253200,Human_Splice_Rec_253240,Human_Splice_Rec_253262,Human_Splice_Rec_253304,Human_Splice_Rec_253322 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_324287,RMVar_hsa_circ_272648,RMVar_hsa_circ_270110,RMVar_hsa_circ_200702,RMVar_hsa_circ_200703,RMVar_hsa_circ_200699,RMVar_hsa_circ_200700,RMVar_hsa_circ_361501 45390 RMVar_ID_45390 Human_SNP_ID_75228096 A-to-I Human chr2 - 63939282 63939282 63939282 CTTCAATCTCTGCCTCCCAGGATCAAGTGATTATCTTGCCTCAGCCACCTGAGTAGCTGGGATTA CTTCAATCTCTGCCTCCCAGGATCAAGTGATTTTCTTGCCTCAGCCACCTGAGTAGCTGGGATTA T A VPS54 Ensembl:ENSG00000143952 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965567882 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15010,RMVar_hsa_circ_61507,RMVar_hsa_circ_56271,RMVar_hsa_circ_281024,RMVar_hsa_circ_337932,RMVar_hsa_circ_112409,RMVar_hsa_circ_200710,RMVar_hsa_circ_303516,RMVar_hsa_circ_23223,RMVar_hsa_circ_274835,RMVar_hsa_circ_58832,RMVar_hsa_circ_200714,RMVar_hsa_circ_200715,RMVar_hsa_circ_200716,RMVar_hsa_circ_51984,RMVar_hsa_circ_20861,RMVar_hsa_circ_63241,RMVar_hsa_circ_200719,RMVar_hsa_circ_97648,RMVar_hsa_circ_120104,RMVar_hsa_circ_200721,RMVar_hsa_circ_90343,RMVar_hsa_circ_200720,RMVar_hsa_circ_94668,RMVar_hsa_circ_200718,RMVar_hsa_circ_200724,RMVar_hsa_circ_29661,RMVar_hsa_circ_61046,RMVar_hsa_circ_327953,RMVar_hsa_circ_200722,RMVar_hsa_circ_288216,RMVar_hsa_circ_46092,RMVar_hsa_circ_200725,RMVar_hsa_circ_200726,RMVar_hsa_circ_200723 45391 RMVar_ID_45391 Human_SNP_ID_75228117 A-to-I Human chr2 - 63939357 63939357 63939357 TGTTTTTTTGTTTTTTTTTGAGGTAGAGTTTCACTCTGTCGCCAGGCTGGAGTGCAGTGGCACAA TGTTTTTTTGTTTTTTTTTGAGGTAGAGTTTCGCTCTGTCGCCAGGCTGGAGTGCAGTGGCACAA T C VPS54 Ensembl:ENSG00000143952 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs191396019 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15010,RMVar_hsa_circ_61507,RMVar_hsa_circ_56271,RMVar_hsa_circ_281024,RMVar_hsa_circ_337932,RMVar_hsa_circ_112409,RMVar_hsa_circ_200710,RMVar_hsa_circ_303516,RMVar_hsa_circ_23223,RMVar_hsa_circ_274835,RMVar_hsa_circ_58832,RMVar_hsa_circ_200714,RMVar_hsa_circ_200715,RMVar_hsa_circ_200716,RMVar_hsa_circ_51984,RMVar_hsa_circ_20861,RMVar_hsa_circ_63241,RMVar_hsa_circ_200719,RMVar_hsa_circ_97648,RMVar_hsa_circ_120104,RMVar_hsa_circ_200721,RMVar_hsa_circ_90343,RMVar_hsa_circ_200720,RMVar_hsa_circ_94668,RMVar_hsa_circ_200718,RMVar_hsa_circ_200724,RMVar_hsa_circ_29661,RMVar_hsa_circ_61046,RMVar_hsa_circ_327953,RMVar_hsa_circ_200722,RMVar_hsa_circ_288216,RMVar_hsa_circ_46092,RMVar_hsa_circ_200725,RMVar_hsa_circ_200726,RMVar_hsa_circ_200723 45392 RMVar_ID_45392 Human_SNP_ID_75228267 A-to-I Human chr2 - 63939872 63939872 63939872 ATGTTTGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCACTTGAACCCGGGAGGTGGAGGTT ATGTTTGTCCCAGCTACTTGGGAGGCTGAGGCGGGAGAATCACTTGAACCCGGGAGGTGGAGGTT T C VPS54 Ensembl:ENSG00000143952 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1265501607 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15010,RMVar_hsa_circ_61507,RMVar_hsa_circ_56271,RMVar_hsa_circ_281024,RMVar_hsa_circ_337932,RMVar_hsa_circ_112409,RMVar_hsa_circ_200710,RMVar_hsa_circ_303516,RMVar_hsa_circ_23223,RMVar_hsa_circ_274835,RMVar_hsa_circ_58832,RMVar_hsa_circ_200714,RMVar_hsa_circ_200715,RMVar_hsa_circ_200716,RMVar_hsa_circ_51984,RMVar_hsa_circ_20861,RMVar_hsa_circ_63241,RMVar_hsa_circ_200719,RMVar_hsa_circ_97648,RMVar_hsa_circ_120104,RMVar_hsa_circ_200721,RMVar_hsa_circ_90343,RMVar_hsa_circ_200720,RMVar_hsa_circ_94668,RMVar_hsa_circ_200718,RMVar_hsa_circ_200724,RMVar_hsa_circ_29661,RMVar_hsa_circ_61046,RMVar_hsa_circ_327953,RMVar_hsa_circ_200722,RMVar_hsa_circ_288216,RMVar_hsa_circ_46092,RMVar_hsa_circ_200725,RMVar_hsa_circ_200726,RMVar_hsa_circ_200723 45393 RMVar_ID_45393 Human_SNP_ID_75228268 A-to-I Human chr2 - 63939876 63939876 63939876 GTGCATGTTTGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCACTTGAACCCGGGAGGTGGA GTGCATGTTTGTCCCAGCTACTTGGGAGGCTGCGGCAGGAGAATCACTTGAACCCGGGAGGTGGA T G VPS54 Ensembl:ENSG00000143952 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs368688769 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15010,RMVar_hsa_circ_61507,RMVar_hsa_circ_56271,RMVar_hsa_circ_281024,RMVar_hsa_circ_337932,RMVar_hsa_circ_112409,RMVar_hsa_circ_200710,RMVar_hsa_circ_303516,RMVar_hsa_circ_23223,RMVar_hsa_circ_274835,RMVar_hsa_circ_58832,RMVar_hsa_circ_200714,RMVar_hsa_circ_200715,RMVar_hsa_circ_200716,RMVar_hsa_circ_51984,RMVar_hsa_circ_20861,RMVar_hsa_circ_63241,RMVar_hsa_circ_200719,RMVar_hsa_circ_97648,RMVar_hsa_circ_120104,RMVar_hsa_circ_200721,RMVar_hsa_circ_90343,RMVar_hsa_circ_200720,RMVar_hsa_circ_94668,RMVar_hsa_circ_200718,RMVar_hsa_circ_200724,RMVar_hsa_circ_29661,RMVar_hsa_circ_61046,RMVar_hsa_circ_327953,RMVar_hsa_circ_200722,RMVar_hsa_circ_288216,RMVar_hsa_circ_46092,RMVar_hsa_circ_200725,RMVar_hsa_circ_200726,RMVar_hsa_circ_200723 45394 RMVar_ID_45394 Human_SNP_ID_75228302 A-to-I Human chr2 - 63939984 63939984 63939984 TGGGAGGCCGAGGCAGGCAGATCACAAGGTCAAGAGATCGAGACCATCCTGGCCAATATGGTGAA TGGGAGGCCGAGGCAGGCAGATCACAAGGTCAGGAGATCGAGACCATCCTGGCCAATATGGTGAA T C VPS54 Ensembl:ENSG00000143952 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1180218614 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15010,RMVar_hsa_circ_61507,RMVar_hsa_circ_56271,RMVar_hsa_circ_281024,RMVar_hsa_circ_337932,RMVar_hsa_circ_112409,RMVar_hsa_circ_200710,RMVar_hsa_circ_303516,RMVar_hsa_circ_23223,RMVar_hsa_circ_274835,RMVar_hsa_circ_58832,RMVar_hsa_circ_200714,RMVar_hsa_circ_200715,RMVar_hsa_circ_200716,RMVar_hsa_circ_51984,RMVar_hsa_circ_20861,RMVar_hsa_circ_63241,RMVar_hsa_circ_200719,RMVar_hsa_circ_97648,RMVar_hsa_circ_120104,RMVar_hsa_circ_200721,RMVar_hsa_circ_90343,RMVar_hsa_circ_200720,RMVar_hsa_circ_94668,RMVar_hsa_circ_200718,RMVar_hsa_circ_200724,RMVar_hsa_circ_29661,RMVar_hsa_circ_61046,RMVar_hsa_circ_327953,RMVar_hsa_circ_200722,RMVar_hsa_circ_288216,RMVar_hsa_circ_46092,RMVar_hsa_circ_200725,RMVar_hsa_circ_200726,RMVar_hsa_circ_200723 45395 RMVar_ID_45395 Human_SNP_ID_75376928 A-to-I Human chr2 + 64548043 64548043 64548043 GAACTCCTGGGCTCAAGTAATTCACCCTCCTCAGCCCCCCAAAGTGCTGGGATTACAGGTGTGAG GAACTCCTGGGCTCAAGTAATTCACCCTCCTCCGCCCCCCAAAGTGCTGGGATTACAGGTGTGAG A C AFTPH Ensembl:ENSG00000119844 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs943062315 Functional Loss SNV dbSNP153 33..33 33 - - - 45396 RMVar_ID_45396 Human_SNP_ID_75381226 A-to-I Human chr2 + 64564491 64564491 64564491 CAGAAACTGGGCAGAAATGGTGGTAGACGCCTATAATCCCAGTTACTTGGGAGGCTAAGGCAGCA CAGAAACTGGGCAGAAATGGTGGTAGACGCCTGTAATCCCAGTTACTTGGGAGGCTAAGGCAGCA A G AFTPH Ensembl:ENSG00000119844 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1481312615 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40532,RMVar_hsa_circ_339066,RMVar_hsa_circ_364556,RMVar_hsa_circ_317773,RMVar_hsa_circ_277839,RMVar_hsa_circ_200748 45397 RMVar_ID_45397 Human_SNP_ID_75464730 A-to-I Human chr2 - 64902275 64902275 64902275 GGGAGGCAGAGGTTGCGGTGAGCCGAGATTGCACCACTGCACTCCAGCCTGGGTAACAAGAGCGA GGGAGGCAGAGGTTGCGGTGAGCCGAGATTGCTCCACTGCACTCCAGCCTGGGTAACAAGAGCGA T A LINC02245 Ensembl:ENSG00000237638 lincRNA exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4671624 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5257,GWAS_ID_5258,GWAS_ID_5259,GWAS_ID_5260,GWAS_ID_5261,GWAS_ID_5262,GWAS_ID_5263,GWAS_ID_5264,GWAS_ID_5265,GWAS_ID_5266,GWAS_ID_5267 45398 RMVar_ID_45398 Human_SNP_ID_75464731 A-to-I Human chr2 - 64902275 64902275 64902275 GGGAGGCAGAGGTTGCGGTGAGCCGAGATTGCACCACTGCACTCCAGCCTGGGTAACAAGAGCGA GGGAGGCAGAGGTTGCGGTGAGCCGAGATTGCGCCACTGCACTCCAGCCTGGGTAACAAGAGCGA T C LINC02245 Ensembl:ENSG00000237638 lincRNA exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4671624 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5257,GWAS_ID_5258,GWAS_ID_5259,GWAS_ID_5260,GWAS_ID_5261,GWAS_ID_5262,GWAS_ID_5263,GWAS_ID_5264,GWAS_ID_5265,GWAS_ID_5266,GWAS_ID_5267 45399 RMVar_ID_45399 Human_SNP_ID_75464732 A-to-I Human chr2 - 64902275 64902275 64902275 GGGAGGCAGAGGTTGCGGTGAGCCGAGATTGCACCACTGCACTCCAGCCTGGGTAACAAGAGCGA GGGAGGCAGAGGTTGCGGTGAGCCGAGATTGCCCCACTGCACTCCAGCCTGGGTAACAAGAGCGA T G LINC02245 Ensembl:ENSG00000237638 lincRNA exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4671624 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5257,GWAS_ID_5258,GWAS_ID_5259,GWAS_ID_5260,GWAS_ID_5261,GWAS_ID_5262,GWAS_ID_5263,GWAS_ID_5264,GWAS_ID_5265,GWAS_ID_5266,GWAS_ID_5267 45400 RMVar_ID_45400 Human_SNP_ID_75488923 A-to-I Human chr2 + 65004496 65004473 65004496 TTTTGTAGAGACAAGAGTTTCACCATGTTGTCAAGGCTAGCCTTGAACTCCTGGCTTCACATAAT TTTTGTAGAG_______________________AGGCTAGCCTTGAACTCCTGGCTTCACATAAT GACAAGAGTTTCACCATGTTGTCA G SLC1A4 Ensembl:ENSG00000115902 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1192725572 Functional Loss DEL dbSNP153 11..33 33 - - - RMVar_hsa_circ_8768,RMVar_hsa_circ_80531,RMVar_hsa_circ_99455,RMVar_hsa_circ_102248,RMVar_hsa_circ_200757,RMVar_hsa_circ_106034,RMVar_hsa_circ_200758,RMVar_hsa_circ_291278,RMVar_hsa_circ_200760,RMVar_hsa_circ_82593,RMVar_hsa_circ_200761,RMVar_hsa_circ_368641,RMVar_hsa_circ_200759,RMVar_hsa_circ_375681,RMVar_hsa_circ_200763,RMVar_hsa_circ_200764,RMVar_hsa_circ_375243,RMVar_hsa_circ_315199,RMVar_hsa_circ_200766,RMVar_hsa_circ_200767,RMVar_hsa_circ_200765 45401 RMVar_ID_45401 Human_SNP_ID_75489913 A-to-I Human chr2 + 65008534 65008534 65008534 ATGGTGGCACATGCTTGTAGTCCCAGCTACTCAGGAGGCTGAGGTAAGAGGATTGCTTAGACCCT ATGGTGGCACATGCTTGTAGTCCCAGCTACTCTGGAGGCTGAGGTAAGAGGATTGCTTAGACCCT A T SLC1A4 Ensembl:ENSG00000115902 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs546290294 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8768,RMVar_hsa_circ_80531,RMVar_hsa_circ_99455,RMVar_hsa_circ_102248,RMVar_hsa_circ_200757,RMVar_hsa_circ_106034,RMVar_hsa_circ_200758,RMVar_hsa_circ_291278,RMVar_hsa_circ_200760,RMVar_hsa_circ_82593,RMVar_hsa_circ_200761,RMVar_hsa_circ_368641,RMVar_hsa_circ_200759,RMVar_hsa_circ_375681,RMVar_hsa_circ_200763,RMVar_hsa_circ_200764,RMVar_hsa_circ_375243,RMVar_hsa_circ_315199,RMVar_hsa_circ_200766,RMVar_hsa_circ_200767,RMVar_hsa_circ_200765 45402 RMVar_ID_45402 Human_SNP_ID_75489919 A-to-I Human chr2 + 65008560 65008560 65008560 CTACTCAGGAGGCTGAGGTAAGAGGATTGCTTAGACCCTGGAGATCAAGGCTGCAGTGAGCCGTG CTACTCAGGAGGCTGAGGTAAGAGGATTGCTTTGACCCTGGAGATCAAGGCTGCAGTGAGCCGTG A T SLC1A4 Ensembl:ENSG00000115902 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1436267790 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8768,RMVar_hsa_circ_80531,RMVar_hsa_circ_99455,RMVar_hsa_circ_102248,RMVar_hsa_circ_200757,RMVar_hsa_circ_106034,RMVar_hsa_circ_200758,RMVar_hsa_circ_291278,RMVar_hsa_circ_200760,RMVar_hsa_circ_82593,RMVar_hsa_circ_200761,RMVar_hsa_circ_368641,RMVar_hsa_circ_200759,RMVar_hsa_circ_375681,RMVar_hsa_circ_200763,RMVar_hsa_circ_200764,RMVar_hsa_circ_375243,RMVar_hsa_circ_315199,RMVar_hsa_circ_200766,RMVar_hsa_circ_200767,RMVar_hsa_circ_200765 45403 RMVar_ID_45403 Human_SNP_ID_75490961 A-to-I Human chr2 + 65012767 65012767 65012767 TTAGACTAAAAAAAAGAAATTGGGGCAGGCGCAGTGGCTCATGCCTGTAATCCCGGCACTTTGGG TTAGACTAAAAAAAAGAAATTGGGGCAGGCGCGGTGGCTCATGCCTGTAATCCCGGCACTTTGGG A G SLC1A4 Ensembl:ENSG00000115902 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947722242 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8768,RMVar_hsa_circ_80531,RMVar_hsa_circ_102248,RMVar_hsa_circ_200757,RMVar_hsa_circ_106034,RMVar_hsa_circ_200758,RMVar_hsa_circ_200760,RMVar_hsa_circ_82593,RMVar_hsa_circ_200761,RMVar_hsa_circ_368641,RMVar_hsa_circ_375681,RMVar_hsa_circ_200764,RMVar_hsa_circ_375243,RMVar_hsa_circ_200769,RMVar_hsa_circ_200766,RMVar_hsa_circ_200767,RMVar_hsa_circ_374395,RMVar_hsa_circ_354679,RMVar_hsa_circ_200768 45404 RMVar_ID_45404 Human_SNP_ID_75503216 A-to-I Human chr2 - 65060527 65060527 65060527 CGAGGCCTCGCTATGTTGCCCGGACTGGTCTCAAACTCCTGAACTCAAGCAATCCTCCCTCCTTG CGAGGCCTCGCTATGTTGCCCGGACTGGTCTCCAACTCCTGAACTCAAGCAATCCTCCCTCCTTG T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs902605521 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2658236,Human_RBP_ID_13939651 45405 RMVar_ID_45405 Human_SNP_ID_75511877 A-to-I Human chr2 - 65091664 65091664 65091664 AAAATTAGCCGGGTGTGGTGGCATGTGCCTGTAGTCCCAGCTACTCAGGAGGCTCAGGTGGAAGG AAAATTAGCCGGGTGTGGTGGCATGTGCCTGTGGTCCCAGCTACTCAGGAGGCTCAGGTGGAAGG T C RAB1A Ensembl:ENSG00000138069 Protein coding intron GSE47997;GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 23474544,29129909,31158229 RNA-Seq:(High) rs550326023 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_200775,RMVar_hsa_circ_200774,RMVar_hsa_circ_361917,RMVar_hsa_circ_20271,RMVar_hsa_circ_200776,RMVar_hsa_circ_275997,RMVar_hsa_circ_278716,RMVar_hsa_circ_200777 45406 RMVar_ID_45406 Human_SNP_ID_75511890 A-to-I Human chr2 - 65091690 65091690 65091690 CGAGACTCTGTCTCTACAAAAAAGAAAAAATTAGCCGGGTGTGGTGGCATGTGCCTGTAGTCCCA CGAGACTCTGTCTCTACAAAAAAGAAAAAATTCGCCGGGTGTGGTGGCATGTGCCTGTAGTCCCA T G RAB1A Ensembl:ENSG00000138069 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs991305903 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_200775,RMVar_hsa_circ_200774,RMVar_hsa_circ_361917,RMVar_hsa_circ_20271,RMVar_hsa_circ_200776,RMVar_hsa_circ_275997,RMVar_hsa_circ_278716,RMVar_hsa_circ_200777 45407 RMVar_ID_45407 Human_SNP_ID_75511891 A-to-I Human chr2 - 65091693 65091692 65091694 TAGCGAGACTCTGTCTCTACAAAAAAGAAAAAATTAGCCGGGTGTGGTGGCATGTGCCTGTAGTC TAGCGAGACTCTGTCTCTACAAAAAAGAAAA__TTAGCCGGGTGTGGTGGCATGTGCCTGTAGTC ATT A RAB1A Ensembl:ENSG00000138069 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1182475629 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_200775,RMVar_hsa_circ_200774,RMVar_hsa_circ_361917,RMVar_hsa_circ_20271,RMVar_hsa_circ_200776,RMVar_hsa_circ_275997,RMVar_hsa_circ_278716,RMVar_hsa_circ_200777 45408 RMVar_ID_45408 Human_SNP_ID_75511891 A-to-I Human chr2 - 65091694 65091692 65091694 GTAGCGAGACTCTGTCTCTACAAAAAAGAAAAAATTAGCCGGGTGTGGTGGCATGTGCCTGTAGT GTAGCGAGACTCTGTCTCTACAAAAAAGAAAA__TTAGCCGGGTGTGGTGGCATGTGCCTGTAGT ATT A RAB1A Ensembl:ENSG00000138069 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1182475629 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_200775,RMVar_hsa_circ_200774,RMVar_hsa_circ_361917,RMVar_hsa_circ_20271,RMVar_hsa_circ_200776,RMVar_hsa_circ_275997,RMVar_hsa_circ_278716,RMVar_hsa_circ_200777 45409 RMVar_ID_45409 Human_SNP_ID_75511902 A-to-I Human chr2 - 65091724 65091724 65091724 GTCCAGGAATTTGAGACCAGCCTGGGCAATGTAGCGAGACTCTGTCTCTACAAAAAAGAAAAAAT GTCCAGGAATTTGAGACCAGCCTGGGCAATGTGGCGAGACTCTGTCTCTACAAAAAAGAAAAAAT T C RAB1A Ensembl:ENSG00000138069 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1226125271 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_200775,RMVar_hsa_circ_200774,RMVar_hsa_circ_361917,RMVar_hsa_circ_20271,RMVar_hsa_circ_200776,RMVar_hsa_circ_275997,RMVar_hsa_circ_278716,RMVar_hsa_circ_200777 45410 RMVar_ID_45410 Human_SNP_ID_75512008 A-to-I Human chr2 - 65092125 65092125 65092125 GGGACCACAGGCGCACGCCAGCATACTTGGCTAATTTTTGGATTTTTAGTAGAGACAGGGTTTCA GGGACCACAGGCGCACGCCAGCATACTTGGCTGATTTTTGGATTTTTAGTAGAGACAGGGTTTCA T C RAB1A Ensembl:ENSG00000138069 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1158894044 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_200775,RMVar_hsa_circ_200774,RMVar_hsa_circ_361917,RMVar_hsa_circ_20271,RMVar_hsa_circ_200776,RMVar_hsa_circ_275997,RMVar_hsa_circ_278716,RMVar_hsa_circ_200777 45411 RMVar_ID_45411 Human_SNP_ID_75512613 A-to-I Human chr2 - 65094428 65094428 65094428 AGGCATGTGCCACCACGCCGGGCTAATTTTGTATTTTTAGTAGAGATGGGGTTTCTCCATGTTGG AGGCATGTGCCACCACGCCGGGCTAATTTTGTGTTTTTAGTAGAGATGGGGTTTCTCCATGTTGG T C RAB1A Ensembl:ENSG00000138069 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs200484812 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_200775,RMVar_hsa_circ_200774,RMVar_hsa_circ_361917,RMVar_hsa_circ_20271,RMVar_hsa_circ_200776,RMVar_hsa_circ_275997,RMVar_hsa_circ_278716,RMVar_hsa_circ_200777 45412 RMVar_ID_45412 Human_SNP_ID_75512954 A-to-I Human chr2 - 65095655 65095655 65095655 TAGTTCCATTTTACACATAACTTCAGCTAGGCATGTTGCCTCATGCCTGTAATCCCAGCACTTTG TAGTTCCATTTTACACATAACTTCAGCTAGGCGTGTTGCCTCATGCCTGTAATCCCAGCACTTTG T C RAB1A Ensembl:ENSG00000138069 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1157867156 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_200775,RMVar_hsa_circ_200774,RMVar_hsa_circ_361917,RMVar_hsa_circ_20271,RMVar_hsa_circ_200776,RMVar_hsa_circ_275997,RMVar_hsa_circ_278716,RMVar_hsa_circ_200777 45413 RMVar_ID_45413 Human_SNP_ID_75512999 A-to-I Human chr2 - 65095846 65095846 65095846 CCCAGCCTTCCGATAATTTTTGTATTTTTCGTAGAGATGGGATTTCGCCATGTTGGCCAGGCTGG CCCAGCCTTCCGATAATTTTTGTATTTTTCGTGGAGATGGGATTTCGCCATGTTGGCCAGGCTGG T C RAB1A Ensembl:ENSG00000138069 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs950092954 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_200775,RMVar_hsa_circ_200774,RMVar_hsa_circ_361917,RMVar_hsa_circ_20271,RMVar_hsa_circ_200776,RMVar_hsa_circ_275997,RMVar_hsa_circ_278716,RMVar_hsa_circ_200777 45414 RMVar_ID_45414 Human_SNP_ID_75513075 A-to-I Human chr2 - 65096044 65096044 65096044 GGTTCAAGCAGTTCTCTTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCGTGCGCCACCACAC GGTTCAAGCAGTTCTCTTGCCTCAGCCTCCTGGGTAGCTGGGATTACAGGCGTGCGCCACCACAC T C RAB1A Ensembl:ENSG00000138069 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1000095435 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_200775,RMVar_hsa_circ_200774,RMVar_hsa_circ_361917,RMVar_hsa_circ_20271,RMVar_hsa_circ_200776,RMVar_hsa_circ_275997,RMVar_hsa_circ_278716,RMVar_hsa_circ_200777 45415 RMVar_ID_45415 Human_SNP_ID_75513463 A-to-I Human chr2 - 65097768 65097768 65097768 TTCAAGATTACTTAAGCCTCATTGAATTTTCTATTCATGAAGCAGAGAAACTCATGTTTTAAGTC TTCAAGATTACTTAAGCCTCATTGAATTTTCTTTTCATGAAGCAGAGAAACTCATGTTTTAAGTC T A RAB1A Ensembl:ENSG00000138069 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6729273 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5268,GWAS_ID_5269,GWAS_ID_5270,GWAS_ID_5271,GWAS_ID_5272,GWAS_ID_5273,GWAS_ID_5274,GWAS_ID_5275,GWAS_ID_5276,GWAS_ID_5277,GWAS_ID_5278,GWAS_ID_5279,GWAS_ID_5280,GWAS_ID_5281,GWAS_ID_5282,GWAS_ID_5283,GWAS_ID_5284,GWAS_ID_5285,GWAS_ID_5286,GWAS_ID_5287,GWAS_ID_5288,GWAS_ID_5289,GWAS_ID_5290,GWAS_ID_5291,GWAS_ID_5292,GWAS_ID_5293,GWAS_ID_5294,GWAS_ID_5295,GWAS_ID_5296,GWAS_ID_5297,GWAS_ID_5298,GWAS_ID_5299,GWAS_ID_5300,GWAS_ID_5301,GWAS_ID_5302,GWAS_ID_5303,GWAS_ID_5304,GWAS_ID_5305 RMVar_hsa_circ_200775,RMVar_hsa_circ_200774,RMVar_hsa_circ_361917,RMVar_hsa_circ_20271,RMVar_hsa_circ_200776,RMVar_hsa_circ_275997,RMVar_hsa_circ_278716,RMVar_hsa_circ_200777 45416 RMVar_ID_45416 Human_SNP_ID_75513464 A-to-I Human chr2 - 65097768 65097768 65097768 TTCAAGATTACTTAAGCCTCATTGAATTTTCTATTCATGAAGCAGAGAAACTCATGTTTTAAGTC TTCAAGATTACTTAAGCCTCATTGAATTTTCTGTTCATGAAGCAGAGAAACTCATGTTTTAAGTC T C RAB1A Ensembl:ENSG00000138069 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6729273 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5268,GWAS_ID_5269,GWAS_ID_5270,GWAS_ID_5271,GWAS_ID_5272,GWAS_ID_5273,GWAS_ID_5274,GWAS_ID_5275,GWAS_ID_5276,GWAS_ID_5277,GWAS_ID_5278,GWAS_ID_5279,GWAS_ID_5280,GWAS_ID_5281,GWAS_ID_5282,GWAS_ID_5283,GWAS_ID_5284,GWAS_ID_5285,GWAS_ID_5286,GWAS_ID_5287,GWAS_ID_5288,GWAS_ID_5289,GWAS_ID_5290,GWAS_ID_5291,GWAS_ID_5292,GWAS_ID_5293,GWAS_ID_5294,GWAS_ID_5295,GWAS_ID_5296,GWAS_ID_5297,GWAS_ID_5298,GWAS_ID_5299,GWAS_ID_5300,GWAS_ID_5301,GWAS_ID_5302,GWAS_ID_5303,GWAS_ID_5304,GWAS_ID_5305 RMVar_hsa_circ_200775,RMVar_hsa_circ_200774,RMVar_hsa_circ_361917,RMVar_hsa_circ_20271,RMVar_hsa_circ_200776,RMVar_hsa_circ_275997,RMVar_hsa_circ_278716,RMVar_hsa_circ_200777 45417 RMVar_ID_45417 Human_SNP_ID_75513836 A-to-I Human chr2 - 65099338 65099338 65099338 ATTCTGAATAAAATTTCATGGCAGGTACTTGCAAGAAGCAGTTATAATTTTAAAAGTTTAACATT ATTCTGAATAAAATTTCATGGCAGGTACTTGCGAGAAGCAGTTATAATTTTAAAAGTTTAACATT T C RAB1A Ensembl:ENSG00000138069 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs9784118 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5306,GWAS_ID_5307,GWAS_ID_5308,GWAS_ID_5309,GWAS_ID_5310,GWAS_ID_5311,GWAS_ID_5312,GWAS_ID_5313,GWAS_ID_5314,GWAS_ID_5315,GWAS_ID_5316,GWAS_ID_5317,GWAS_ID_5318,GWAS_ID_5319,GWAS_ID_5320,GWAS_ID_5321,GWAS_ID_5322,GWAS_ID_5323,GWAS_ID_5324,GWAS_ID_5325,GWAS_ID_5326,GWAS_ID_5327,GWAS_ID_5328,GWAS_ID_5329,GWAS_ID_5330,GWAS_ID_5331,GWAS_ID_5332,GWAS_ID_5333,GWAS_ID_5334,GWAS_ID_5335,GWAS_ID_5336,GWAS_ID_5337,GWAS_ID_5338,GWAS_ID_5339,GWAS_ID_5340,GWAS_ID_5341,GWAS_ID_5342,GWAS_ID_5343,GWAS_ID_5344,GWAS_ID_5345,GWAS_ID_5346 RMVar_hsa_circ_200774,RMVar_hsa_circ_20271,RMVar_hsa_circ_200778,RMVar_hsa_circ_275997,RMVar_hsa_circ_200777,RMVar_hsa_circ_278839 45418 RMVar_ID_45418 Human_SNP_ID_75514160 A-to-I Human chr2 - 65100577 65100577 65100577 TTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGATCT TTTTGTATTTTTAGTAGAGACAGGGTTTCACCGTGTTGGCCAGGCTGGTCTTGAACTCCTGATCT T C RAB1A Ensembl:ENSG00000138069 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs149597821 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_200774,RMVar_hsa_circ_20271,RMVar_hsa_circ_200778,RMVar_hsa_circ_275997,RMVar_hsa_circ_200777,RMVar_hsa_circ_278839 45419 RMVar_ID_45419 Human_SNP_ID_75516152 A-to-I Human chr2 - 65107245 65107245 65107245 GCCTCCAACATGATGAAACTCCCGTCTTTACTAGAAATACAAAAATTAGCTGGGTGTGTTAGCAC GCCTCCAACATGATGAAACTCCCGTCTTTACTGGAAATACAAAAATTAGCTGGGTGTGTTAGCAC T C RAB1A Ensembl:ENSG00000138069 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs544805662 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_200774 45420 RMVar_ID_45420 Human_SNP_ID_75516245 A-to-I Human chr2 - 65107590 65107590 65107590 CCAGCTACTCAGGAGGCTGAGGCCTGAGAATCACTTGAACACCTGGAGGCAGAGGTTGCAGTGAA CCAGCTACTCAGGAGGCTGAGGCCTGAGAATCGCTTGAACACCTGGAGGCAGAGGTTGCAGTGAA T C RAB1A Ensembl:ENSG00000138069 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1297005004 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569694 RMVar_hsa_circ_200774 45421 RMVar_ID_45421 Human_SNP_ID_75518267 A-to-I Human chr2 - 65115037 65115037 65115037 TTATCATATGGTGGAAGGTGGAAAGGCAAGTGAGTATGTCAAGACAGAGAGCAAGAAGGGGCTTG TTATCATATGGTGGAAGGTGGAAAGGCAAGTGTGTATGTCAAGACAGAGAGCAAGAAGGGGCTTG T A RAB1A Ensembl:ENSG00000138069 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1019303 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5347,GWAS_ID_5348,GWAS_ID_5349,GWAS_ID_5350,GWAS_ID_5351,GWAS_ID_5352,GWAS_ID_5353,GWAS_ID_5354,GWAS_ID_5355,GWAS_ID_5356,GWAS_ID_5357,GWAS_ID_5358,GWAS_ID_5359,GWAS_ID_5360,GWAS_ID_5361,GWAS_ID_5362,GWAS_ID_5363,GWAS_ID_5364,GWAS_ID_5365,GWAS_ID_5366,GWAS_ID_5367,GWAS_ID_5368,GWAS_ID_5369,GWAS_ID_5370,GWAS_ID_5371,GWAS_ID_5372,GWAS_ID_5373,GWAS_ID_5374,GWAS_ID_5375,GWAS_ID_5376,GWAS_ID_5377,GWAS_ID_5378,GWAS_ID_5379,GWAS_ID_5380,GWAS_ID_5381,GWAS_ID_5382,GWAS_ID_5383,GWAS_ID_5384,GWAS_ID_5385,GWAS_ID_5386,GWAS_ID_5387 RMVar_hsa_circ_200774 45422 RMVar_ID_45422 Human_SNP_ID_75518268 A-to-I Human chr2 - 65115037 65115037 65115037 TTATCATATGGTGGAAGGTGGAAAGGCAAGTGAGTATGTCAAGACAGAGAGCAAGAAGGGGCTTG TTATCATATGGTGGAAGGTGGAAAGGCAAGTGGGTATGTCAAGACAGAGAGCAAGAAGGGGCTTG T C RAB1A Ensembl:ENSG00000138069 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1019303 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5347,GWAS_ID_5348,GWAS_ID_5349,GWAS_ID_5350,GWAS_ID_5351,GWAS_ID_5352,GWAS_ID_5353,GWAS_ID_5354,GWAS_ID_5355,GWAS_ID_5356,GWAS_ID_5357,GWAS_ID_5358,GWAS_ID_5359,GWAS_ID_5360,GWAS_ID_5361,GWAS_ID_5362,GWAS_ID_5363,GWAS_ID_5364,GWAS_ID_5365,GWAS_ID_5366,GWAS_ID_5367,GWAS_ID_5368,GWAS_ID_5369,GWAS_ID_5370,GWAS_ID_5371,GWAS_ID_5372,GWAS_ID_5373,GWAS_ID_5374,GWAS_ID_5375,GWAS_ID_5376,GWAS_ID_5377,GWAS_ID_5378,GWAS_ID_5379,GWAS_ID_5380,GWAS_ID_5381,GWAS_ID_5382,GWAS_ID_5383,GWAS_ID_5384,GWAS_ID_5385,GWAS_ID_5386,GWAS_ID_5387 RMVar_hsa_circ_200774 45423 RMVar_ID_45423 Human_SNP_ID_75518347 A-to-I Human chr2 - 65115436 65115436 65115436 GAAGGTTGGTTTTGAATTGTGTTCTGTGGAGCATACTTAAAGTGAGTGAAGAAGAAAAATTTATG GAAGGTTGGTTTTGAATTGTGTTCTGTGGAGCGTACTTAAAGTGAGTGAAGAAGAAAAATTTATG T C RAB1A Ensembl:ENSG00000138069 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1019305 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5388,GWAS_ID_5389,GWAS_ID_5390,GWAS_ID_5391,GWAS_ID_5392,GWAS_ID_5393,GWAS_ID_5394,GWAS_ID_5395,GWAS_ID_5396,GWAS_ID_5397,GWAS_ID_5398,GWAS_ID_5399,GWAS_ID_5400,GWAS_ID_5401,GWAS_ID_5402,GWAS_ID_5403,GWAS_ID_5404,GWAS_ID_5405,GWAS_ID_5406,GWAS_ID_5407,GWAS_ID_5408,GWAS_ID_5409,GWAS_ID_5410,GWAS_ID_5411,GWAS_ID_5412,GWAS_ID_5413,GWAS_ID_5414,GWAS_ID_5415,GWAS_ID_5416,GWAS_ID_5417,GWAS_ID_5418,GWAS_ID_5419,GWAS_ID_5420,GWAS_ID_5421,GWAS_ID_5422,GWAS_ID_5423,GWAS_ID_5424,GWAS_ID_5425,GWAS_ID_5426,GWAS_ID_5427,GWAS_ID_5428 RMVar_hsa_circ_200774 45424 RMVar_ID_45424 Human_SNP_ID_75518797 A-to-I Human chr2 - 65117158 65117158 65117158 AAGAGGCTGAGGCAAGAGGGTTGCTTGAGCCCAGAAGTTGGAGGCTGCCGTGAACTGTGATTGCA AAGAGGCTGAGGCAAGAGGGTTGCTTGAGCCCGGAAGTTGGAGGCTGCCGTGAACTGTGATTGCA T C RAB1A Ensembl:ENSG00000138069 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs996548041 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_200774 45425 RMVar_ID_45425 Human_SNP_ID_75518802 A-to-I Human chr2 - 65117189 65117189 65117189 GTGGTTGGTGTGCTTGTGGTCCCAGCTACTCAAGAGGCTGAGGCAAGAGGGTTGCTTGAGCCCAG GTGGTTGGTGTGCTTGTGGTCCCAGCTACTCAGGAGGCTGAGGCAAGAGGGTTGCTTGAGCCCAG T C RAB1A Ensembl:ENSG00000138069 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1176019633 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_200774 45426 RMVar_ID_45426 Human_SNP_ID_75519154 A-to-I Human chr2 - 65118554 65118554 65118554 AGAACTGCTTGAACCCGGGAGGCAGAGGTTGCAGTGAGCCGAGATTGTGCTACTGCACTTCAGCC AGAACTGCTTGAACCCGGGAGGCAGAGGTTGCCGTGAGCCGAGATTGTGCTACTGCACTTCAGCC T G RAB1A Ensembl:ENSG00000138069 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1162957241 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_200774 45427 RMVar_ID_45427 Human_SNP_ID_75519175 A-to-I Human chr2 - 65118657 65118657 65118657 CCTGGGCAACACAGTGAAACCCTGTCTCTACTAAAATACAAAAAATCAGCTGGGTGTGGCAGCAT CCTGGGCAACACAGTGAAACCCTGTCTCTACTCAAATACAAAAAATCAGCTGGGTGTGGCAGCAT T G RAB1A Ensembl:ENSG00000138069 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs556651166 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_200774 45428 RMVar_ID_45428 Human_SNP_ID_75519198 A-to-I Human chr2 - 65118751 65118751 65118751 CCTTTGGGCCGGGTGCGGGGGCTGACGCCTGTAGTCCTAGCACTTTGGGAGGCTGAGGTGGGCGG CCTTTGGGCCGGGTGCGGGGGCTGACGCCTGTGGTCCTAGCACTTTGGGAGGCTGAGGTGGGCGG T C RAB1A Ensembl:ENSG00000138069 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1019446875 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13941057 RMVar_hsa_circ_200774 45429 RMVar_ID_45429 Human_SNP_ID_75519261 A-to-I Human chr2 - 65118971 65118971 65118971 TGTATCAGGCTGGTTTTGAACTCCTGAGCTCAAGCAATCCTCACTCTTTGACCTCCCAACGTGCT TGTATCAGGCTGGTTTTGAACTCCTGAGCTCAGGCAATCCTCACTCTTTGACCTCCCAACGTGCT T C RAB1A Ensembl:ENSG00000138069 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs77546827 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1378807,Human_RBP_ID_6940478 RMVar_hsa_circ_200774 45430 RMVar_ID_45430 Human_SNP_ID_75519717 A-to-I Human chr2 - 65120309 65120306 65120309 TGGGATTACAGGCTGCGCCACCACGCCCAGCTAATTTTTTGTATTTATAGTAAAGACGGAGTTTC TGGGATTACAGGCTGCGCCACCACGCCCAGCT___TTTTTGTATTTATAGTAAAGACGGAGTTTC AATT A RAB1A Ensembl:ENSG00000138069 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1297544194 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_200774 45431 RMVar_ID_45431 Human_SNP_ID_75519719 A-to-I Human chr2 - 65120309 65120309 65120309 TGGGATTACAGGCTGCGCCACCACGCCCAGCTAATTTTTTGTATTTATAGTAAAGACGGAGTTTC TGGGATTACAGGCTGCGCCACCACGCCCAGCTGATTTTTTGTATTTATAGTAAAGACGGAGTTTC T C RAB1A Ensembl:ENSG00000138069 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1362237292 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_200774 45432 RMVar_ID_45432 Human_SNP_ID_75520395 A-to-I Human chr2 - 65122548 65122548 65122548 TTGAGTGTCTGTTTTTTGAGATATAGGGTCTTACTCTGTCACGCAGGCTACAGTGCAGTGATGCA TTGAGTGTCTGTTTTTTGAGATATAGGGTCTTGCTCTGTCACGCAGGCTACAGTGCAGTGATGCA T C RAB1A Ensembl:ENSG00000138069 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1464675355 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13941171,Human_RBP_ID_27697605 RMVar_hsa_circ_200774 45433 RMVar_ID_45433 Human_SNP_ID_75520552 A-to-I Human chr2 - 65123047 65123043 65123047 AGTTTTGACTATACCTATGTGATGGTTTCACTATTTGTAGTTTGAATAGTTCAGTTTTATTTTGG AGTTTTGACTATACCTATGTGATGGTTTCACT____GTAGTTTGAATAGTTCAGTTTTATTTTGG CAAAT C RAB1A Ensembl:ENSG00000138069 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1228143895 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_23880364 RMVar_hsa_circ_200774 45434 RMVar_ID_45434 Human_SNP_ID_75520554 A-to-I Human chr2 - 65123047 65123047 65123047 AGTTTTGACTATACCTATGTGATGGTTTCACTATTTGTAGTTTGAATAGTTCAGTTTTATTTTGG AGTTTTGACTATACCTATGTGATGGTTTCACTTTTTGTAGTTTGAATAGTTCAGTTTTATTTTGG T A RAB1A Ensembl:ENSG00000138069 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7583197 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23880364 RMVar_hsa_circ_200774 45435 RMVar_ID_45435 Human_SNP_ID_75520555 A-to-I Human chr2 - 65123047 65123047 65123047 AGTTTTGACTATACCTATGTGATGGTTTCACTATTTGTAGTTTGAATAGTTCAGTTTTATTTTGG AGTTTTGACTATACCTATGTGATGGTTTCACTGTTTGTAGTTTGAATAGTTCAGTTTTATTTTGG T C RAB1A Ensembl:ENSG00000138069 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7583197 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23880364 RMVar_hsa_circ_200774 45436 RMVar_ID_45436 Human_SNP_ID_75520754 A-to-I Human chr2 - 65123660 65123660 65123660 CACCACACCCGGCTAATTTTTGTAGTTTTAGTAGAGACAGGGTTTCACTATGTTGGCCAGGCTGG CACCACACCCGGCTAATTTTTGTAGTTTTAGTGGAGACAGGGTTTCACTATGTTGGCCAGGCTGG T C RAB1A Ensembl:ENSG00000138069 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1306114827 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_200774 45437 RMVar_ID_45437 Human_SNP_ID_75520765 A-to-I Human chr2 - 65123714 65123713 65123714 TTAAGTGATTCTTCCACCTCAGCCTCTCAAGTAGCTGGGAGTACAGGTGTGTGCCACCACACCCG TTAAGTGATTCTTCCACCTCAGCCTCTCAAGT_GCTGGGAGTACAGGTGTGTGCCACCACACCCG CT C RAB1A Ensembl:ENSG00000138069 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1206173668 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_200774 45438 RMVar_ID_45438 Human_SNP_ID_75521009 A-to-I Human chr2 - 65124630 65124630 65124630 CAGCCTGGCCAACATGGCAAAACCCTGTCTCTACTAAGCATAGAAAAATTAATTGGGTGTGGTCG CAGCCTGGCCAACATGGCAAAACCCTGTCTCTGCTAAGCATAGAAAAATTAATTGGGTGTGGTCG T C RAB1A Ensembl:ENSG00000138069 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1011376066 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_200774 45439 RMVar_ID_45439 Human_SNP_ID_75521017 A-to-I Human chr2 - 65124690 65124690 65124690 ATAATCACAGCACTTTGGGAGGCCCAGGCGGTAGATCACCTGAGGTCAGGAGTTTGAGACCAGCC ATAATCACAGCACTTTGGGAGGCCCAGGCGGTGGATCACCTGAGGTCAGGAGTTTGAGACCAGCC T C RAB1A Ensembl:ENSG00000138069 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1317146730 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_200774 45440 RMVar_ID_45440 Human_SNP_ID_75521491 A-to-I Human chr2 - 65126202 65126202 65126202 TCAAGCGATTTTCCTGCCTTGGTCTCCTGAGTAGCTGGGATTACAGGCATTTGCCACCATAACCA TCAAGCGATTTTCCTGCCTTGGTCTCCTGAGTGGCTGGGATTACAGGCATTTGCCACCATAACCA T C RAB1A Ensembl:ENSG00000138069 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1013064418 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_200774 45441 RMVar_ID_45441 Human_SNP_ID_75521503 A-to-I Human chr2 - 65126251 65126251 65126251 GGAGTGCAGTGGCGCGATCTTGGCTCACTGCAATCTCTGCCTCCTGGGTTCAAGCGATTTTCCTG GGAGTGCAGTGGCGCGATCTTGGCTCACTGCAGTCTCTGCCTCCTGGGTTCAAGCGATTTTCCTG T C RAB1A Ensembl:ENSG00000138069 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285753866 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_200774 45442 RMVar_ID_45442 Human_SNP_ID_75521518 A-to-I Human chr2 - 65126300 65126296 65126300 TTTTCTTTTTCTTTTTTTCGAGATGGAGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGCGCG TTTTCTTTTTCTTTTTTTCGAGATGGAGTCTC____TGTCACCCAGGCTGGAGTGCAGTGGCGCG AGAGT A RAB1A Ensembl:ENSG00000138069 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1028202879 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_200774 45443 RMVar_ID_45443 Human_SNP_ID_75521833 A-to-I Human chr2 - 65127602 65127602 65127602 CCTGCCTCAGATTCCCGAGAAGTTGGGATTACAGGCATGTGCCACCACTCCCGGCTAATTTTGTA CCTGCCTCAGATTCCCGAGAAGTTGGGATTACCGGCATGTGCCACCACTCCCGGCTAATTTTGTA T G RAB1A Ensembl:ENSG00000138069 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs186971495 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569699 RMVar_hsa_circ_200774 45444 RMVar_ID_45444 Human_SNP_ID_75521840 A-to-I Human chr2 - 65127643 65127643 65127643 CCTCTCACCGCCACCTCCGCCTCCTGGGTTCAAGTGATTCTCCTGCCTCAGATTCCCGAGAAGTT CCTCTCACCGCCACCTCCGCCTCCTGGGTTCAGGTGATTCTCCTGCCTCAGATTCCCGAGAAGTT T C RAB1A Ensembl:ENSG00000138069 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1161040878 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569699 RMVar_hsa_circ_200774 45445 RMVar_ID_45445 Human_SNP_ID_75521865 A-to-I Human chr2 - 65127735 65127732 65127736 AGCAAGACTCCGTCTCAAAAAAAAAATTATTTATTGTTTTGAGACGGAGTTTCAATCTTGTTGCC AGCAAGACTCCGTCTCAAAAAAAAAATTATT____GTTTTGAGACGGAGTTTCAATCTTGTTGCC CAATA C RAB1A Ensembl:ENSG00000138069 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs985578158 Functional Loss DEL dbSNP153 32..35 33 - - - RMVar_hsa_circ_200774 45446 RMVar_ID_45446 Human_SNP_ID_75546544 A-to-I Human chr2 - 65221006 65221006 65221006 CAGCCTCCTGAATACTAGGACTACCGGCATGTACCACCATACCCAGCTAATCTTTAAAAATTATT CAGCCTCCTGAATACTAGGACTACCGGCATGTGCCACCATACCCAGCTAATCTTTAAAAATTATT T C AC007318.3 Ensembl:ENSG00000273763 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956533273 Functional Loss SNV dbSNP153 33..33 33 - - - 45447 RMVar_ID_45447 Human_SNP_ID_75549302 A-to-I Human chr2 + 65230986 65230986 65230986 TGAGGCAGGAGAATTACTTGTACCTGGGAGGCAGAGGTTGCAGTGAGCCAAGATCACGCCACTGC TGAGGCAGGAGAATTACTTGTACCTGGGAGGCGGAGGTTGCAGTGAGCCAAGATCACGCCACTGC A G ACTR2 Ensembl:ENSG00000138071 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1164762925 Functional Loss SNV dbSNP153 33..33 33 - - - 45448 RMVar_ID_45448 Human_SNP_ID_75550597 A-to-I Human chr2 + 65236136 65236136 65236136 CCAGGCTGGTGGATTACATGAGGTCAGGAGTTAGAGACCAGCCTGGCCAACATGGTGAAACCCCG CCAGGCTGGTGGATTACATGAGGTCAGGAGTTGGAGACCAGCCTGGCCAACATGGTGAAACCCCG A G ACTR2 Ensembl:ENSG00000138071 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs894015713 Functional Loss SNV dbSNP153 33..33 33 - - - 45449 RMVar_ID_45449 Human_SNP_ID_75550634 A-to-I Human chr2 + 65236261 65236261 65236261 CTTGGGAGGCTGAGGCAGAATTGCTGGAACCTAGGAGGCAGAGGTTGCAGTGAGCTGCGATGACG CTTGGGAGGCTGAGGCAGAATTGCTGGAACCTGGGAGGCAGAGGTTGCAGTGAGCTGCGATGACG A G ACTR2 Ensembl:ENSG00000138071 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1380572699 Functional Loss SNV dbSNP153 33..33 33 - - - 45450 RMVar_ID_45450 Human_SNP_ID_75550760 A-to-I Human chr2 + 65236693 65236693 65236693 ACCTCCGCCTCCCAGGTTCAAGTGATTCTCATACCTCAGCCTCCCAAGTAACTGGGATTACAGGC ACCTCCGCCTCCCAGGTTCAAGTGATTCTCATTCCTCAGCCTCCCAAGTAACTGGGATTACAGGC A T ACTR2 Ensembl:ENSG00000138071 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs751330979 Functional Loss SNV dbSNP153 33..33 33 - - - 45451 RMVar_ID_45451 Human_SNP_ID_75550906 A-to-I Human chr2 + 65237351 65237351 65237351 AACCTCCCAGGCTCAAGTGATCCTCCCACCTCAGTCTCTGGAATAGCTGGGACTATAGCACATGC AACCTCCCAGGCTCAAGTGATCCTCCCACCTCCGTCTCTGGAATAGCTGGGACTATAGCACATGC A C ACTR2 Ensembl:ENSG00000138071 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1314835168 Functional Loss SNV dbSNP153 33..33 33 - - - 45452 RMVar_ID_45452 Human_SNP_ID_75551032 A-to-I Human chr2 + 65237698 65237698 65237698 CATAGTGAGACCCCATCTCTACAAAAAATTTTAAAACTTACGCTAGGCGTGGTGGCTCACTCCTG CATAGTGAGACCCCATCTCTACAAAAAATTTTGAAACTTACGCTAGGCGTGGTGGCTCACTCCTG A G ACTR2 Ensembl:ENSG00000138071 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs557567335 Functional Loss SNV dbSNP153 33..33 33 - - - 45453 RMVar_ID_45453 Human_SNP_ID_75554604 A-to-I Human chr2 + 65251439 65251439 65251439 GCCGGAGTGCAATAGTGCAATCTTGGCTTACCACAACCTCCACCTCCTGGGTTCAAGTGATTTTC GCCGGAGTGCAATAGTGCAATCTTGGCTTACCGCAACCTCCACCTCCTGGGTTCAAGTGATTTTC A G ACTR2 Ensembl:ENSG00000138071 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1242873330 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_287124,RMVar_hsa_circ_359306,RMVar_hsa_circ_292043,RMVar_hsa_circ_99199,RMVar_hsa_circ_200784,RMVar_hsa_circ_109381,RMVar_hsa_circ_200779,RMVar_hsa_circ_200780,RMVar_hsa_circ_292163,RMVar_hsa_circ_363293,RMVar_hsa_circ_200781,RMVar_hsa_circ_272590,RMVar_hsa_circ_200783,RMVar_hsa_circ_200785,RMVar_hsa_circ_373901 45454 RMVar_ID_45454 Human_SNP_ID_75554618 A-to-I Human chr2 + 65251491 65251491 65251491 TCAAGTGATTTTCCTGCCTCAGCCTCCCAAGTATTTGGGATTACAGGCATGTGCCACCACACCTG TCAAGTGATTTTCCTGCCTCAGCCTCCCAAGTGTTTGGGATTACAGGCATGTGCCACCACACCTG A G ACTR2 Ensembl:ENSG00000138071 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs978739255 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_287124,RMVar_hsa_circ_359306,RMVar_hsa_circ_292043,RMVar_hsa_circ_99199,RMVar_hsa_circ_200784,RMVar_hsa_circ_109381,RMVar_hsa_circ_200779,RMVar_hsa_circ_200780,RMVar_hsa_circ_292163,RMVar_hsa_circ_363293,RMVar_hsa_circ_200781,RMVar_hsa_circ_272590,RMVar_hsa_circ_200783,RMVar_hsa_circ_200785,RMVar_hsa_circ_373901 45455 RMVar_ID_45455 Human_SNP_ID_75555003 A-to-I Human chr2 + 65252844 65252844 65252844 GTAAAATTAGCTGGGTGTGGTTGCACATGCCTATAATCCCAGCCACTTGAGAGGCTGAGGTGAGA GTAAAATTAGCTGGGTGTGGTTGCACATGCCTGTAATCCCAGCCACTTGAGAGGCTGAGGTGAGA A G ACTR2 Ensembl:ENSG00000138071 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs963279964 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_287124,RMVar_hsa_circ_359306,RMVar_hsa_circ_292043,RMVar_hsa_circ_99199,RMVar_hsa_circ_200784,RMVar_hsa_circ_109381,RMVar_hsa_circ_200779,RMVar_hsa_circ_200780,RMVar_hsa_circ_292163,RMVar_hsa_circ_363293,RMVar_hsa_circ_200781,RMVar_hsa_circ_272590,RMVar_hsa_circ_200783,RMVar_hsa_circ_200785,RMVar_hsa_circ_373901 45456 RMVar_ID_45456 Human_SNP_ID_75556402 A-to-I Human chr2 + 65258441 65258441 65258441 CTACAAAAAAAATACAAAAATTTGCCAGGCGTAGTGGCACGTGCCTGTAGTCCTAGCTAGTTGAG CTACAAAAAAAATACAAAAATTTGCCAGGCGTCGTGGCACGTGCCTGTAGTCCTAGCTAGTTGAG A C ACTR2 Ensembl:ENSG00000138071 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1222270673 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_292043,RMVar_hsa_circ_99199,RMVar_hsa_circ_200784,RMVar_hsa_circ_109381,RMVar_hsa_circ_200779,RMVar_hsa_circ_200780,RMVar_hsa_circ_292163,RMVar_hsa_circ_200781,RMVar_hsa_circ_272590,RMVar_hsa_circ_59492,RMVar_hsa_circ_200785,RMVar_hsa_circ_373901,RMVar_hsa_circ_315653 45457 RMVar_ID_45457 Human_SNP_ID_75556525 A-to-I Human chr2 + 65258993 65258993 65258993 GTAACCTTTTTTTTTTCTTTCTGTTTTGAGACAGGGTTTCCTCACTCTGTTGCTCAGGCTGCAGT GTAACCTTTTTTTTTTCTTTCTGTTTTGAGACGGGGTTTCCTCACTCTGTTGCTCAGGCTGCAGT A G ACTR2 Ensembl:ENSG00000138071 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs919332978 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_292043,RMVar_hsa_circ_99199,RMVar_hsa_circ_200784,RMVar_hsa_circ_109381,RMVar_hsa_circ_200779,RMVar_hsa_circ_200780,RMVar_hsa_circ_292163,RMVar_hsa_circ_200781,RMVar_hsa_circ_272590,RMVar_hsa_circ_59492,RMVar_hsa_circ_200785,RMVar_hsa_circ_373901,RMVar_hsa_circ_315653 45458 RMVar_ID_45458 Human_SNP_ID_75556678 A-to-I Human chr2 + 65259608 65259608 65259608 AAAATTAGCCAGGCGTGGTGGCACATGCCTGTAATCTCAGCTACTTGGGGGGCTGAGGTATGAGA AAAATTAGCCAGGCGTGGTGGCACATGCCTGTGATCTCAGCTACTTGGGGGGCTGAGGTATGAGA A G ACTR2 Ensembl:ENSG00000138071 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1448729100 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_292043,RMVar_hsa_circ_99199,RMVar_hsa_circ_200784,RMVar_hsa_circ_109381,RMVar_hsa_circ_200779,RMVar_hsa_circ_200780,RMVar_hsa_circ_292163,RMVar_hsa_circ_200781,RMVar_hsa_circ_272590,RMVar_hsa_circ_59492,RMVar_hsa_circ_200785,RMVar_hsa_circ_373901,RMVar_hsa_circ_315653 45459 RMVar_ID_45459 Human_SNP_ID_75557049 A-to-I Human chr2 + 65261004 65261004 65261004 CGCCCAGCTCAGCCTCCCAAAGTGCTGGGATTACAGACGTGAGCCACCACGCCCAGCCTGGCATA CGCCCAGCTCAGCCTCCCAAAGTGCTGGGATTTCAGACGTGAGCCACCACGCCCAGCCTGGCATA A T ACTR2 Ensembl:ENSG00000138071 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs974447845 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_292043,RMVar_hsa_circ_99199,RMVar_hsa_circ_200784,RMVar_hsa_circ_109381,RMVar_hsa_circ_200779,RMVar_hsa_circ_200780,RMVar_hsa_circ_292163,RMVar_hsa_circ_200781,RMVar_hsa_circ_272590,RMVar_hsa_circ_59492,RMVar_hsa_circ_200785,RMVar_hsa_circ_373901,RMVar_hsa_circ_315653 45460 RMVar_ID_45460 Human_SNP_ID_75557058 A-to-I Human chr2 + 65261026 65261026 65261026 TGCTGGGATTACAGACGTGAGCCACCACGCCCAGCCTGGCATAACATTTTTAAAAGCAAAACAGA TGCTGGGATTACAGACGTGAGCCACCACGCCCGGCCTGGCATAACATTTTTAAAAGCAAAACAGA A G ACTR2 Ensembl:ENSG00000138071 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs268861 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5429,GWAS_ID_5430,GWAS_ID_5431,GWAS_ID_5432,GWAS_ID_5433,GWAS_ID_5434,GWAS_ID_5435,GWAS_ID_5436,GWAS_ID_5437,GWAS_ID_5438,GWAS_ID_5439,GWAS_ID_5440,GWAS_ID_5441,GWAS_ID_5442,GWAS_ID_5443,GWAS_ID_5444,GWAS_ID_5445,GWAS_ID_5446,GWAS_ID_5447,GWAS_ID_5448,GWAS_ID_5449,GWAS_ID_5450,GWAS_ID_5451,GWAS_ID_5452,GWAS_ID_5453,GWAS_ID_5454,GWAS_ID_5455,GWAS_ID_5456,GWAS_ID_5457,GWAS_ID_5458,GWAS_ID_5459,GWAS_ID_5460,GWAS_ID_5461,GWAS_ID_5462,GWAS_ID_5463,GWAS_ID_5464,GWAS_ID_5465,GWAS_ID_5466,GWAS_ID_5467,GWAS_ID_5468,GWAS_ID_5469,GWAS_ID_5470,GWAS_ID_5471,GWAS_ID_5472,GWAS_ID_5473,GWAS_ID_5474,GWAS_ID_5475,GWAS_ID_5476,GWAS_ID_5477,GWAS_ID_5478,GWAS_ID_5479,GWAS_ID_5480,GWAS_ID_5481,GWAS_ID_5482,GWAS_ID_5483,GWAS_ID_5484 RMVar_hsa_circ_292043,RMVar_hsa_circ_99199,RMVar_hsa_circ_200784,RMVar_hsa_circ_109381,RMVar_hsa_circ_200779,RMVar_hsa_circ_200780,RMVar_hsa_circ_292163,RMVar_hsa_circ_200781,RMVar_hsa_circ_272590,RMVar_hsa_circ_59492,RMVar_hsa_circ_200785,RMVar_hsa_circ_373901,RMVar_hsa_circ_315653 45461 RMVar_ID_45461 Human_SNP_ID_75570641 A-to-I Human chr2 - 65313805 65313805 65313805 GCGGTGCGTGTACTGCAGGGACATGTTCAACCACGAGGAGAACCGCCGGGGCCACTGCCAGGACG GCGGTGCGTGTACTGCAGGGACATGTTCAACCGCGAGGAGAACCGCCGGGGCCACTGCCAGGACG T C SPRED2 Ensembl:ENSG00000198369 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1462562322 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104607,RMVar_hsa_circ_200787 45462 RMVar_ID_45462 Human_SNP_ID_75594852 A-to-I Human chr2 - 65408686 65408686 65408686 GTCCCAGCTACTCAGGAGGCTGAGGCAGAAGAATTGCTTGATCCCAGAAGGCAGAGGTTGCAGAT GTCCCAGCTACTCAGGAGGCTGAGGCAGAAGACTTGCTTGATCCCAGAAGGCAGAGGTTGCAGAT T G SPRED2 Ensembl:ENSG00000198369 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1463641442 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122122,RMVar_hsa_circ_200791,RMVar_hsa_circ_321419 45463 RMVar_ID_45463 Human_SNP_ID_75594867 A-to-I Human chr2 - 65408751 65408751 65408751 TATAGTGGAACCCCATCTCTACTAAAAATACAAAAATTAGCTGGGTGTGGTGGCACGTGACTATT TATAGTGGAACCCCATCTCTACTAAAAATACAGAAATTAGCTGGGTGTGGTGGCACGTGACTATT T C SPRED2 Ensembl:ENSG00000198369 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1211923658 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122122,RMVar_hsa_circ_200791,RMVar_hsa_circ_321419 45464 RMVar_ID_45464 Human_SNP_ID_76274439 A-to-I Human chr2 - 68056273 68056273 68056273 TGGTGAAACCCCGTCTCTCCTAAAAAAATACAAAAATTAGCTGGGCATGGTGGCACGCACCTGTA TGGTGAAACCCCGTCTCTCCTAAAAAAATACAGAAATTAGCTGGGCATGGTGGCACGCACCTGTA T C C1D Ensembl:ENSG00000197223 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1276306633 Functional Loss SNV dbSNP153 33..33 33 - - - 45465 RMVar_ID_45465 Human_SNP_ID_76293107 A-to-I Human chr2 - 68133677 68133677 68133677 CATGATCTCGTCTCACCGCAGACTCCACCTCCAGGTTCAAGGGGTTCTCCTGCCTCAGCCTCCCG CATGATCTCGTCTCACCGCAGACTCCACCTCCTGGTTCAAGGGGTTCTCCTGCCTCAGCCTCCCG T A AC017083.3,WDR92 Ensembl:ENSG00000273398,Ensembl:ENSG00000243667 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs370940043 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9785,RMVar_hsa_circ_278880,RMVar_hsa_circ_283619,RMVar_hsa_circ_346441,RMVar_hsa_circ_277015,RMVar_hsa_circ_200824,RMVar_hsa_circ_200826,RMVar_hsa_circ_200827,RMVar_hsa_circ_200825 45466 RMVar_ID_45466 Human_SNP_ID_76293108 A-to-I Human chr2 - 68133677 68133677 68133677 CATGATCTCGTCTCACCGCAGACTCCACCTCCAGGTTCAAGGGGTTCTCCTGCCTCAGCCTCCCG CATGATCTCGTCTCACCGCAGACTCCACCTCCGGGTTCAAGGGGTTCTCCTGCCTCAGCCTCCCG T C AC017083.3,WDR92 Ensembl:ENSG00000273398,Ensembl:ENSG00000243667 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs370940043 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9785,RMVar_hsa_circ_278880,RMVar_hsa_circ_283619,RMVar_hsa_circ_346441,RMVar_hsa_circ_277015,RMVar_hsa_circ_200824,RMVar_hsa_circ_200826,RMVar_hsa_circ_200827,RMVar_hsa_circ_200825 45467 RMVar_ID_45467 Human_SNP_ID_76305361 A-to-I Human chr2 - 68180117 68180117 68180117 ATGTCCCTCAGTAACGTTAAGTGCTAGTTGTGATTTTATACATAAAGGCCAGAAGCTGTCTGAGG ATGTCCCTCAGTAACGTTAAGTGCTAGTTGTGGTTTTATACATAAAGGCCAGAAGCTGTCTGAGG T C AC017083.3,PPP3R1 Ensembl:ENSG00000273398,Ensembl:ENSG00000221823 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs532369961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_554103,Human_RBP_ID_1922065,Human_RBP_ID_3632114,Human_RBP_ID_6942378,Human_RBP_ID_8201515,Human_RBP_ID_17960092,Human_RBP_ID_18180570,Human_RBP_ID_18318511,Human_RBP_ID_23881229,Human_RBP_ID_24490013,Human_RBP_ID_26484447,Human_RBP_ID_27697791 Human_miRNA_ID_854214,Human_miRNA_ID_1523848 45468 RMVar_ID_45468 Human_SNP_ID_76305463 A-to-I Human chr2 - 68180548 68180548 68180548 ATATACTTGATTCAGAAACAAAACAATAGAGTACAAAAGTGCCAAGCAGAACATAAAACATCCTT ATATACTTGATTCAGAAACAAAACAATAGAGTGCAAAAGTGCCAAGCAGAACATAAAACATCCTT T C AC017083.3,PPP3R1 Ensembl:ENSG00000273398,Ensembl:ENSG00000221823 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947740832 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_554125,Human_RBP_ID_4614274,Human_RBP_ID_6942401,Human_RBP_ID_17276635,Human_RBP_ID_17960103,Human_RBP_ID_23881240,Human_RBP_ID_26486412,Human_RBP_ID_27697802 45469 RMVar_ID_45469 Human_SNP_ID_76311741 A-to-I Human chr2 - 68202671 68202671 68202671 CCTGTAATCCCAGCACTTTGGGAGACCGAGGCAAGTGGATCACCTGAGGTCGGGAGTTCGTGACC CCTGTAATCCCAGCACTTTGGGAGACCGAGGCGAGTGGATCACCTGAGGTCGGGAGTTCGTGACC T C AC017083.3,PPP3R1 Ensembl:ENSG00000273398,Ensembl:ENSG00000221823 Protein coding,Protein coding intron,intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs984281498 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_363919 45470 RMVar_ID_45470 Human_SNP_ID_76323408 A-to-I Human chr2 - 68245188 68245188 68245188 CCAGCTAATTTTTGTGGAGACAGGGTCTTGCCATGTTGCGCAGGCTGGTCTCAAACTCCTGAGCT CCAGCTAATTTTTGTGGAGACAGGGTCTTGCCGTGTTGCGCAGGCTGGTCTCAAACTCCTGAGCT T C AC017083.3,PPP3R1 Ensembl:ENSG00000273398,Ensembl:ENSG00000221823 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1478730237 Functional Loss SNV dbSNP153 33..33 33 - - - 45471 RMVar_ID_45471 Human_SNP_ID_76323432 A-to-I Human chr2 - 68245286 68245286 68245286 GCGATCTCAGCTTATTGCAGCCTCCACCTCCCAGGCTCAAGCCATCCTCCCTCCTCAGCCTCCCA GCGATCTCAGCTTATTGCAGCCTCCACCTCCCGGGCTCAAGCCATCCTCCCTCCTCAGCCTCCCA T C AC017083.3,PPP3R1 Ensembl:ENSG00000273398,Ensembl:ENSG00000221823 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1370034615 Functional Loss SNV dbSNP153 33..33 33 - - - 45472 RMVar_ID_45472 Human_SNP_ID_76323451 A-to-I Human chr2 - 68245336 68245336 68245336 CTTTTTGGAGACAGGATCTTGCTATTTTGCCCAGGTTGGAGTGCGGTGGTGCGATCTCAGCTTAT CTTTTTGGAGACAGGATCTTGCTATTTTGCCCGGGTTGGAGTGCGGTGGTGCGATCTCAGCTTAT T C AC017083.3,PPP3R1 Ensembl:ENSG00000273398,Ensembl:ENSG00000221823 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1181248690 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22994741 45473 RMVar_ID_45473 Human_SNP_ID_76336259 A-to-I Human chr2 - 68296859 68296859 68296859 CGAGGTGGGTGGATCACGAGGTCAGGAGTTCAAGACCAGACTGGCCAACATGGTGAAACCCCGTC CGAGGTGGGTGGATCACGAGGTCAGGAGTTCAGGACCAGACTGGCCAACATGGTGAAACCCCGTC T C CNRIP1 Ensembl:ENSG00000119865 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1160383398 Functional Loss SNV dbSNP153 33..33 33 - - - 45474 RMVar_ID_45474 Human_SNP_ID_76353855 A-to-I Human chr2 - 68365395 68365395 68365395 CACTGACACCCTGGTAAGTGGCACCTTCGCTCACCTTCTTCACAAGGTAGCCCTCTCTGATCCGC CACTGACACCCTGGTAAGTGGCACCTTCGCTCCCCTTCTTCACAAGGTAGCCCTCTCTGATCCGC T G AC015969.1 Ensembl:ENSG00000203395 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs891553764 Functional Loss SNV dbSNP153 33..33 33 - - - 45475 RMVar_ID_45475 Human_SNP_ID_76586512 A-to-I Human chr2 - 69319095 69319095 69319095 AAAATTAGCCGGGCGTGGTGGCAGGCCCCTGTAGCCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTAGCCGGGCGTGGTGGCAGGCCCCTGTTGCCCCAGCTACTCGGGAGGCTGAGGCAGGAGA T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1368105340 Functional Loss SNV dbSNP153 33..33 33 - - - 45476 RMVar_ID_45476 Human_SNP_ID_76586825 A-to-I Human chr2 - 69320525 69320525 69320525 CCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGTCACCGTGTCCTGCCCAGACATATCAAA CCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGTCACCGTGTCCTGCCCAGACATATCAAA T C GFPT1 Ensembl:ENSG00000198380 Protein coding 3'UTR GSE38233;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;esophageal squamous carcinoma cells,EC109 cell line - 24183664,32596459 RNA-Seq:(High) rs1470515105 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266238 45477 RMVar_ID_45477 Human_SNP_ID_76586865 A-to-I Human chr2 - 69320741 69320741 69320741 CTCTGTTGCCCAGGCTGGCATGCAGTGCTGCAATCTTGGCTGACTGCAACTTCCACCTCCCGTGT CTCTGTTGCCCAGGCTGGCATGCAGTGCTGCAGTCTTGGCTGACTGCAACTTCCACCTCCCGTGT T C GFPT1 Ensembl:ENSG00000198380 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1051676273 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_554220,Human_RBP_ID_13946207 RMVar_hsa_circ_266238 45478 RMVar_ID_45478 Human_SNP_ID_76588269 A-to-I Human chr2 - 69326995 69326995 69326995 AACACAAAAAGAACGATCAAGGTGCCCCACTCAGTGGACTGCTTGCAGGGCATTCTCAGCGTGAT AACACAAAAAGAACGATCAAGGTGCCCCACTCGGTGGACTGCTTGCAGGGCATTCTCAGCGTGAT T C GFPT1 Ensembl:ENSG00000198380 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs17854372 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6943160,Human_RBP_ID_8851904,Human_RBP_ID_9296568,Human_RBP_ID_22076331,Human_RBP_ID_22449832,Human_RBP_ID_26819810 Human_Splice_Rec_255722,Human_Splice_Rec_255723,Human_Splice_Rec_255758,Human_Splice_Rec_255759,Human_Splice_Rec_255792,Human_Splice_Rec_255793,Human_Splice_Rec_255824,Human_Splice_Rec_255825 Human_miRNA_ID_1793789 RMVar_hsa_circ_15973,RMVar_hsa_circ_200878,RMVar_hsa_circ_266238,RMVar_hsa_circ_72018,RMVar_hsa_circ_200877,RMVar_hsa_circ_267372,RMVar_hsa_circ_23588 45479 RMVar_ID_45479 Human_SNP_ID_76595173 A-to-I Human chr2 - 69354799 69354799 69354799 TTTCCCAGAGTGGTCTTGAACTCGTGGGCTCAAGTGATCTGCCTGCCTAGGCCTCCTGAAGTGCT TTTCCCAGAGTGGTCTTGAACTCGTGGGCTCAGGTGATCTGCCTGCCTAGGCCTCCTGAAGTGCT T C GFPT1 Ensembl:ENSG00000198380 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs536740783 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_641,RMVar_hsa_circ_15973,RMVar_hsa_circ_200878,RMVar_hsa_circ_266238,RMVar_hsa_circ_72018,RMVar_hsa_circ_8086,RMVar_hsa_circ_65994,RMVar_hsa_circ_362385,RMVar_hsa_circ_316554,RMVar_hsa_circ_65068,RMVar_hsa_circ_200879,RMVar_hsa_circ_332326,RMVar_hsa_circ_281270,RMVar_hsa_circ_78392,RMVar_hsa_circ_24919,RMVar_hsa_circ_62487,RMVar_hsa_circ_200888,RMVar_hsa_circ_200889,RMVar_hsa_circ_200886,RMVar_hsa_circ_200887,RMVar_hsa_circ_374577,RMVar_hsa_circ_270171,RMVar_hsa_circ_200902,RMVar_hsa_circ_200897,RMVar_hsa_circ_200898,RMVar_hsa_circ_289718,RMVar_hsa_circ_347335,RMVar_hsa_circ_285752,RMVar_hsa_circ_277098,RMVar_hsa_circ_200903,RMVar_hsa_circ_88414,RMVar_hsa_circ_200901,RMVar_hsa_circ_329214,RMVar_hsa_circ_287894,RMVar_hsa_circ_200904,RMVar_hsa_circ_200906,RMVar_hsa_circ_200905,RMVar_hsa_circ_265310,RMVar_hsa_circ_348993,RMVar_hsa_circ_200909,RMVar_hsa_circ_101249,RMVar_hsa_circ_290906,RMVar_hsa_circ_341559,RMVar_hsa_circ_282433,RMVar_hsa_circ_200911,RMVar_hsa_circ_200912,RMVar_hsa_circ_200910 45480 RMVar_ID_45480 Human_SNP_ID_76595639 A-to-I Human chr2 - 69356555 69356555 69356555 TAGTGCTAATGGATTTTTTTCCCTCCCTAGGAAGGTGCTTTTGCACTTGTGTTTAAAAGTGTTCA TAGTGCTAATGGATTTTTTTCCCTCCCTAGGAGGGTGCTTTTGCACTTGTGTTTAAAAGTGTTCA T C GFPT1 Ensembl:ENSG00000198380 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs780082221 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_554295,Human_RBP_ID_921518,Human_RBP_ID_8523881,Human_RBP_ID_22595569,Human_RBP_ID_22667386,Human_RBP_ID_24560352,Human_RBP_ID_25559820 Human_Splice_Rec_255698,Human_Splice_Rec_255699,Human_Splice_Rec_255736,Human_Splice_Rec_255737,Human_Splice_Rec_255772,Human_Splice_Rec_255773,Human_Splice_Rec_255802,Human_Splice_Rec_255803 Human_miRNA_ID_2018598,Human_miRNA_ID_2023692,Human_miRNA_ID_2179973,Human_miRNA_ID_2182081,Human_miRNA_ID_2310313,Human_miRNA_ID_2312333,Human_miRNA_ID_2498423,Human_miRNA_ID_2606206,Human_miRNA_ID_2654107,Human_miRNA_ID_2804944,Human_miRNA_ID_2808089,Human_miRNA_ID_2811233,Human_miRNA_ID_3034591 RMVar_hsa_circ_641,RMVar_hsa_circ_15973,RMVar_hsa_circ_200878,RMVar_hsa_circ_266238,RMVar_hsa_circ_72018,RMVar_hsa_circ_8086,RMVar_hsa_circ_65994,RMVar_hsa_circ_362385,RMVar_hsa_circ_316554,RMVar_hsa_circ_65068,RMVar_hsa_circ_200879,RMVar_hsa_circ_332326,RMVar_hsa_circ_281270,RMVar_hsa_circ_78392,RMVar_hsa_circ_24919,RMVar_hsa_circ_62487,RMVar_hsa_circ_200888,RMVar_hsa_circ_200889,RMVar_hsa_circ_200886,RMVar_hsa_circ_200887,RMVar_hsa_circ_374577,RMVar_hsa_circ_270171,RMVar_hsa_circ_200902,RMVar_hsa_circ_200897,RMVar_hsa_circ_200898,RMVar_hsa_circ_289718,RMVar_hsa_circ_347335,RMVar_hsa_circ_285752,RMVar_hsa_circ_277098,RMVar_hsa_circ_200903,RMVar_hsa_circ_88414,RMVar_hsa_circ_200901,RMVar_hsa_circ_329214,RMVar_hsa_circ_287894,RMVar_hsa_circ_200904,RMVar_hsa_circ_200906,RMVar_hsa_circ_200905,RMVar_hsa_circ_265310,RMVar_hsa_circ_348993,RMVar_hsa_circ_200909,RMVar_hsa_circ_101249,RMVar_hsa_circ_290906,RMVar_hsa_circ_341559,RMVar_hsa_circ_282433,RMVar_hsa_circ_200911,RMVar_hsa_circ_200912,RMVar_hsa_circ_200910,RMVar_hsa_circ_200913,RMVar_hsa_circ_274222,RMVar_hsa_circ_321099 45481 RMVar_ID_45481 Human_SNP_ID_76596525 A-to-I Human chr2 - 69360171 69360171 69360171 GCACGTGCCACCACGCCTGGCTAATGTTTTGTATTTTTAGTAGAGACAGGGTTTCGCCATGTTGA GCACGTGCCACCACGCCTGGCTAATGTTTTGTGTTTTTAGTAGAGACAGGGTTTCGCCATGTTGA T C GFPT1 Ensembl:ENSG00000198380 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs751569442 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_641,RMVar_hsa_circ_15973,RMVar_hsa_circ_200878,RMVar_hsa_circ_266238,RMVar_hsa_circ_72018,RMVar_hsa_circ_8086,RMVar_hsa_circ_65994,RMVar_hsa_circ_362385,RMVar_hsa_circ_281270,RMVar_hsa_circ_24919,RMVar_hsa_circ_62487,RMVar_hsa_circ_200886,RMVar_hsa_circ_200887,RMVar_hsa_circ_374577,RMVar_hsa_circ_270171,RMVar_hsa_circ_200902,RMVar_hsa_circ_200897,RMVar_hsa_circ_200898,RMVar_hsa_circ_347335,RMVar_hsa_circ_285752,RMVar_hsa_circ_277098,RMVar_hsa_circ_200903,RMVar_hsa_circ_88414,RMVar_hsa_circ_329214,RMVar_hsa_circ_287894,RMVar_hsa_circ_200904,RMVar_hsa_circ_200906,RMVar_hsa_circ_200905,RMVar_hsa_circ_348993,RMVar_hsa_circ_105635,RMVar_hsa_circ_101249,RMVar_hsa_circ_290906,RMVar_hsa_circ_282433,RMVar_hsa_circ_200911,RMVar_hsa_circ_200912,RMVar_hsa_circ_200910,RMVar_hsa_circ_122374,RMVar_hsa_circ_200913,RMVar_hsa_circ_274222,RMVar_hsa_circ_321099,RMVar_hsa_circ_313810,RMVar_hsa_circ_344239,RMVar_hsa_circ_288191,RMVar_hsa_circ_200915,RMVar_hsa_circ_200916,RMVar_hsa_circ_200917,RMVar_hsa_circ_200914,RMVar_hsa_circ_200918 45482 RMVar_ID_45482 Human_SNP_ID_76596956 A-to-I Human chr2 - 69361864 69361864 69361864 GTGATCTTCCTGCCTCAGCCTCCTGAGTAGCTAGGATCACAGGCTTGCACCACCACACCCAGCTA GTGATCTTCCTGCCTCAGCCTCCTGAGTAGCTGGGATCACAGGCTTGCACCACCACACCCAGCTA T C GFPT1 Ensembl:ENSG00000198380 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459911277 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_641,RMVar_hsa_circ_15973,RMVar_hsa_circ_200878,RMVar_hsa_circ_266238,RMVar_hsa_circ_72018,RMVar_hsa_circ_8086,RMVar_hsa_circ_65994,RMVar_hsa_circ_362385,RMVar_hsa_circ_281270,RMVar_hsa_circ_24919,RMVar_hsa_circ_62487,RMVar_hsa_circ_200886,RMVar_hsa_circ_200887,RMVar_hsa_circ_374577,RMVar_hsa_circ_270171,RMVar_hsa_circ_200902,RMVar_hsa_circ_200897,RMVar_hsa_circ_200898,RMVar_hsa_circ_347335,RMVar_hsa_circ_285752,RMVar_hsa_circ_277098,RMVar_hsa_circ_200903,RMVar_hsa_circ_88414,RMVar_hsa_circ_329214,RMVar_hsa_circ_287894,RMVar_hsa_circ_200904,RMVar_hsa_circ_200906,RMVar_hsa_circ_200905,RMVar_hsa_circ_348993,RMVar_hsa_circ_105635,RMVar_hsa_circ_101249,RMVar_hsa_circ_290906,RMVar_hsa_circ_282433,RMVar_hsa_circ_200911,RMVar_hsa_circ_200912,RMVar_hsa_circ_200910,RMVar_hsa_circ_122374,RMVar_hsa_circ_200913,RMVar_hsa_circ_274222,RMVar_hsa_circ_321099,RMVar_hsa_circ_313810,RMVar_hsa_circ_344239,RMVar_hsa_circ_288191,RMVar_hsa_circ_200915,RMVar_hsa_circ_200916,RMVar_hsa_circ_200917,RMVar_hsa_circ_200914,RMVar_hsa_circ_200918 45483 RMVar_ID_45483 Human_SNP_ID_76597307 A-to-I Human chr2 - 69363242 69363239 69363242 AAAATAAGTTAGGCATTGTGGTGCATGCTTGTAGTCTCAGCTACTCGGGAGACTGAGGTGGGAGG AAAATAAGTTAGGCATTGTGGTGCATGCTTGT___CTCAGCTACTCGGGAGACTGAGGTGGGAGG GACT G GFPT1 Ensembl:ENSG00000198380 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1240055868 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_25559848 RMVar_hsa_circ_641,RMVar_hsa_circ_15973,RMVar_hsa_circ_200878,RMVar_hsa_circ_266238,RMVar_hsa_circ_72018,RMVar_hsa_circ_8086,RMVar_hsa_circ_65994,RMVar_hsa_circ_362385,RMVar_hsa_circ_281270,RMVar_hsa_circ_24919,RMVar_hsa_circ_62487,RMVar_hsa_circ_200886,RMVar_hsa_circ_200887,RMVar_hsa_circ_374577,RMVar_hsa_circ_270171,RMVar_hsa_circ_200902,RMVar_hsa_circ_200897,RMVar_hsa_circ_200898,RMVar_hsa_circ_347335,RMVar_hsa_circ_285752,RMVar_hsa_circ_277098,RMVar_hsa_circ_200903,RMVar_hsa_circ_88414,RMVar_hsa_circ_329214,RMVar_hsa_circ_287894,RMVar_hsa_circ_200904,RMVar_hsa_circ_200906,RMVar_hsa_circ_200905,RMVar_hsa_circ_348993,RMVar_hsa_circ_105635,RMVar_hsa_circ_101249,RMVar_hsa_circ_290906,RMVar_hsa_circ_282433,RMVar_hsa_circ_200911,RMVar_hsa_circ_200912,RMVar_hsa_circ_200910,RMVar_hsa_circ_122374,RMVar_hsa_circ_200913,RMVar_hsa_circ_274222,RMVar_hsa_circ_321099,RMVar_hsa_circ_313810,RMVar_hsa_circ_344239,RMVar_hsa_circ_288191,RMVar_hsa_circ_200915,RMVar_hsa_circ_200916,RMVar_hsa_circ_200917,RMVar_hsa_circ_200914,RMVar_hsa_circ_200918 45484 RMVar_ID_45484 Human_SNP_ID_76597319 A-to-I Human chr2 - 69363303 69363303 69363303 GTCCAGGAGTTCACGATCAGCCGTGGCAACATAGTGAGACCCTGTCTCTACAAAAAATAAAAAAA GTCCAGGAGTTCACGATCAGCCGTGGCAACATGGTGAGACCCTGTCTCTACAAAAAATAAAAAAA T C GFPT1 Ensembl:ENSG00000198380 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs56712132 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_641,RMVar_hsa_circ_15973,RMVar_hsa_circ_200878,RMVar_hsa_circ_266238,RMVar_hsa_circ_72018,RMVar_hsa_circ_8086,RMVar_hsa_circ_65994,RMVar_hsa_circ_362385,RMVar_hsa_circ_281270,RMVar_hsa_circ_24919,RMVar_hsa_circ_62487,RMVar_hsa_circ_200886,RMVar_hsa_circ_200887,RMVar_hsa_circ_374577,RMVar_hsa_circ_270171,RMVar_hsa_circ_200902,RMVar_hsa_circ_200897,RMVar_hsa_circ_200898,RMVar_hsa_circ_347335,RMVar_hsa_circ_285752,RMVar_hsa_circ_277098,RMVar_hsa_circ_200903,RMVar_hsa_circ_88414,RMVar_hsa_circ_329214,RMVar_hsa_circ_287894,RMVar_hsa_circ_200904,RMVar_hsa_circ_200906,RMVar_hsa_circ_200905,RMVar_hsa_circ_348993,RMVar_hsa_circ_105635,RMVar_hsa_circ_101249,RMVar_hsa_circ_290906,RMVar_hsa_circ_282433,RMVar_hsa_circ_200911,RMVar_hsa_circ_200912,RMVar_hsa_circ_200910,RMVar_hsa_circ_122374,RMVar_hsa_circ_200913,RMVar_hsa_circ_274222,RMVar_hsa_circ_321099,RMVar_hsa_circ_313810,RMVar_hsa_circ_344239,RMVar_hsa_circ_288191,RMVar_hsa_circ_200915,RMVar_hsa_circ_200916,RMVar_hsa_circ_200917,RMVar_hsa_circ_200914,RMVar_hsa_circ_200918 45485 RMVar_ID_45485 Human_SNP_ID_76597742 A-to-I Human chr2 - 69364812 69364812 69364812 TTTTGTAGTTTTAGTAGAGACAGGGTTTCACCATGTTGGTAAGGCTGGTCTTGGACTCCTGACCT TTTTGTAGTTTTAGTAGAGACAGGGTTTCACCGTGTTGGTAAGGCTGGTCTTGGACTCCTGACCT T C GFPT1 Ensembl:ENSG00000198380 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs553832007 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_641,RMVar_hsa_circ_15973,RMVar_hsa_circ_200878,RMVar_hsa_circ_266238,RMVar_hsa_circ_65994,RMVar_hsa_circ_24919,RMVar_hsa_circ_62487,RMVar_hsa_circ_200886,RMVar_hsa_circ_374577,RMVar_hsa_circ_200898,RMVar_hsa_circ_347335,RMVar_hsa_circ_277098,RMVar_hsa_circ_200903,RMVar_hsa_circ_88414,RMVar_hsa_circ_329214,RMVar_hsa_circ_200904,RMVar_hsa_circ_200905,RMVar_hsa_circ_101249,RMVar_hsa_circ_282433,RMVar_hsa_circ_200911,RMVar_hsa_circ_200912,RMVar_hsa_circ_122374,RMVar_hsa_circ_321099,RMVar_hsa_circ_313810,RMVar_hsa_circ_344239,RMVar_hsa_circ_200915,RMVar_hsa_circ_200916,RMVar_hsa_circ_200917,RMVar_hsa_circ_200921,RMVar_hsa_circ_307456,RMVar_hsa_circ_53580 45486 RMVar_ID_45486 Human_SNP_ID_76598623 A-to-I Human chr2 - 69368193 69368193 69368193 TATTTTTAGTAGAGATGGGGTTTCACCATGTTAGCCAGGATAGTCTCGATCTCCTGACCTCGTGA TATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGATAGTCTCGATCTCCTGACCTCGTGA T C GFPT1 Ensembl:ENSG00000198380 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1372059643 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_641,RMVar_hsa_circ_15973,RMVar_hsa_circ_200878,RMVar_hsa_circ_266238,RMVar_hsa_circ_65994,RMVar_hsa_circ_24919,RMVar_hsa_circ_62487,RMVar_hsa_circ_200886,RMVar_hsa_circ_374577,RMVar_hsa_circ_200898,RMVar_hsa_circ_347335,RMVar_hsa_circ_277098,RMVar_hsa_circ_200903,RMVar_hsa_circ_88414,RMVar_hsa_circ_329214,RMVar_hsa_circ_200904,RMVar_hsa_circ_200905,RMVar_hsa_circ_101249,RMVar_hsa_circ_282433,RMVar_hsa_circ_200911,RMVar_hsa_circ_200912,RMVar_hsa_circ_122374,RMVar_hsa_circ_321099,RMVar_hsa_circ_313810,RMVar_hsa_circ_344239,RMVar_hsa_circ_200915,RMVar_hsa_circ_200916,RMVar_hsa_circ_200917,RMVar_hsa_circ_200921,RMVar_hsa_circ_307456,RMVar_hsa_circ_53580 45487 RMVar_ID_45487 Human_SNP_ID_76598635 A-to-I Human chr2 - 69368231 69368231 69368231 CCACAGGCGCCCGCCACAACGCCTGGCTAATTATTTCGTATTTTTAGTAGAGATGGGGTTTCACC CCACAGGCGCCCGCCACAACGCCTGGCTAATTGTTTCGTATTTTTAGTAGAGATGGGGTTTCACC T C GFPT1 Ensembl:ENSG00000198380 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1192645791 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_641,RMVar_hsa_circ_15973,RMVar_hsa_circ_200878,RMVar_hsa_circ_266238,RMVar_hsa_circ_65994,RMVar_hsa_circ_24919,RMVar_hsa_circ_62487,RMVar_hsa_circ_200886,RMVar_hsa_circ_374577,RMVar_hsa_circ_200898,RMVar_hsa_circ_347335,RMVar_hsa_circ_277098,RMVar_hsa_circ_200903,RMVar_hsa_circ_88414,RMVar_hsa_circ_329214,RMVar_hsa_circ_200904,RMVar_hsa_circ_200905,RMVar_hsa_circ_101249,RMVar_hsa_circ_282433,RMVar_hsa_circ_200911,RMVar_hsa_circ_200912,RMVar_hsa_circ_122374,RMVar_hsa_circ_321099,RMVar_hsa_circ_313810,RMVar_hsa_circ_344239,RMVar_hsa_circ_200915,RMVar_hsa_circ_200916,RMVar_hsa_circ_200917,RMVar_hsa_circ_200921,RMVar_hsa_circ_307456,RMVar_hsa_circ_53580 45488 RMVar_ID_45488 Human_SNP_ID_76601257 A-to-I Human chr2 - 69378134 69378134 69378134 CGGGCATGGCGGCGGCCACTGTAATTCCAGCTACTTGGGAGGCTGAGGCAGGAGAATTGCTGGAA CGGGCATGGCGGCGGCCACTGTAATTCCAGCTGCTTGGGAGGCTGAGGCAGGAGAATTGCTGGAA T C GFPT1 Ensembl:ENSG00000198380 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1156342389 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1135039 RMVar_hsa_circ_122374,RMVar_hsa_circ_200917 45489 RMVar_ID_45489 Human_SNP_ID_76601777 A-to-I Human chr2 - 69380349 69380349 69380349 GTGATTTATTTTATTTTACTTTTACATTTTTTATTTTTTTGAGACAGAGTCTCACTGTGTCGCCC GTGATTTATTTTATTTTACTTTTACATTTTTTTTTTTTTTGAGACAGAGTCTCACTGTGTCGCCC T A GFPT1 Ensembl:ENSG00000198380 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs929591959 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6943299,Human_RBP_ID_13946772 RMVar_hsa_circ_122374,RMVar_hsa_circ_200917 45490 RMVar_ID_45490 Human_SNP_ID_76602714 A-to-I Human chr2 - 69384488 69384488 69384488 AGACTGGTCTGCTGACCTCAGGTAATCCACCTACCACAGCCTCCCAAAGTGCTGGGATTACAGGA AGACTGGTCTGCTGACCTCAGGTAATCCACCTGCCACAGCCTCCCAAAGTGCTGGGATTACAGGA T C GFPT1 Ensembl:ENSG00000198380 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs894984727 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122374,RMVar_hsa_circ_200917 45491 RMVar_ID_45491 Human_SNP_ID_76602718 A-to-I Human chr2 - 69384497 69384497 69384497 ATGTTGACCAGACTGGTCTGCTGACCTCAGGTAATCCACCTACCACAGCCTCCCAAAGTGCTGGG ATGTTGACCAGACTGGTCTGCTGACCTCAGGTGATCCACCTACCACAGCCTCCCAAAGTGCTGGG T C GFPT1 Ensembl:ENSG00000198380 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1233962244 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122374,RMVar_hsa_circ_200917 45492 RMVar_ID_45492 Human_SNP_ID_76608049 A-to-I Human chr2 - 69405237 69405237 69405237 AAAAGTAAGCCTATAGTTTTTGGTTTTTTTTTAAGACGGAGTCTTGCTCTGTCACCCAGGCTGGC AAAAGTAAGCCTATAGTTTTTGGTTTTTTTTTGAGACGGAGTCTTGCTCTGTCACCCAGGCTGGC T C NFU1 Ensembl:ENSG00000169599 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs747566471 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17495,RMVar_hsa_circ_281938,RMVar_hsa_circ_352226,RMVar_hsa_circ_71625,RMVar_hsa_circ_200923 45493 RMVar_ID_45493 Human_SNP_ID_76609719 A-to-I Human chr2 - 69412093 69412093 69412093 TGAGCTGACATCATGCCATTGCACTCCAGCCTAGTGACAGAGCGAGACTCCGTCCCCCCGCCAAA TGAGCTGACATCATGCCATTGCACTCCAGCCTGGTGACAGAGCGAGACTCCGTCCCCCCGCCAAA T C NFU1 Ensembl:ENSG00000169599 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1290769723 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17495,RMVar_hsa_circ_281938,RMVar_hsa_circ_71625,RMVar_hsa_circ_200924,RMVar_hsa_circ_332834,RMVar_hsa_circ_200923,RMVar_hsa_circ_300361 45494 RMVar_ID_45494 Human_SNP_ID_76614664 A-to-I Human chr2 - 69429453 69429453 69429453 GGGCTCAAGCAGTCCTCTTGCCTTAGCCTCCTATGTAGCTGGAATTATAGGCACATGCCACCACA GGGCTCAAGCAGTCCTCTTGCCTTAGCCTCCTTTGTAGCTGGAATTATAGGCACATGCCACCACA T A NFU1 Ensembl:ENSG00000169599 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1484233026 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_281938,RMVar_hsa_circ_200924,RMVar_hsa_circ_200923,RMVar_hsa_circ_300361,RMVar_hsa_circ_200925,RMVar_hsa_circ_302649,RMVar_hsa_circ_354344,RMVar_hsa_circ_200927,RMVar_hsa_circ_321850 45495 RMVar_ID_45495 Human_SNP_ID_76622952 A-to-I Human chr2 - 69461647 69461647 69461647 GACTTTGCAGTGAGCCAAGATTGTGTCATTGCACTCCAGCCTGGGCGAGAAGAGCAAAACTCCGC GACTTTGCAGTGAGCCAAGATTGTGTCATTGCCCTCCAGCCTGGGCGAGAAGAGCAAAACTCCGC T G AAK1 Ensembl:ENSG00000115977 Protein coding 3'UTR GSE100210;GSE107867 HepG2 cell line;ASD brains,temporal_cortex - 29129909,30559470 RNA-Seq:(High) rs756641894 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93707,RMVar_hsa_circ_109768,RMVar_hsa_circ_122881,RMVar_hsa_circ_268607,RMVar_hsa_circ_100894,RMVar_hsa_circ_200929,RMVar_hsa_circ_200931,RMVar_hsa_circ_200932,RMVar_hsa_circ_200930 45496 RMVar_ID_45496 Human_SNP_ID_76622971 A-to-I Human chr2 - 69461717 69461717 69461717 CGTGATGGCACGCACCTGTAGTCCCAGTTACTAGGGAGGCTGAGGCAGAATTGCTTGACCCAGGG CGTGATGGCACGCACCTGTAGTCCCAGTTACTCGGGAGGCTGAGGCAGAATTGCTTGACCCAGGG T G AAK1 Ensembl:ENSG00000115977 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs1443815248 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93707,RMVar_hsa_circ_109768,RMVar_hsa_circ_122881,RMVar_hsa_circ_268607,RMVar_hsa_circ_100894,RMVar_hsa_circ_200929,RMVar_hsa_circ_200931,RMVar_hsa_circ_200932,RMVar_hsa_circ_200930 45497 RMVar_ID_45497 Human_SNP_ID_76623005 A-to-I Human chr2 - 69461856 69461856 69461856 CAGGCGCGGTGGCTCACGCTTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGTGGATCACTTGA CAGGCGCGGTGGCTCACGCTTGTAATCCCAGCCCTTTGGGAGGCCGAGGTGGGTGGATCACTTGA T G AAK1 Ensembl:ENSG00000115977 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs548383557 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93707,RMVar_hsa_circ_109768,RMVar_hsa_circ_122881,RMVar_hsa_circ_268607,RMVar_hsa_circ_100894,RMVar_hsa_circ_200929,RMVar_hsa_circ_200931,RMVar_hsa_circ_200932,RMVar_hsa_circ_200930 45498 RMVar_ID_45498 Human_SNP_ID_76623188 A-to-I Human chr2 - 69462619 69462619 69462619 CAGGCGGGAGTGCAGTGGTGTGATCTCGGCTCACTGCAACCTCCATTTTCCGAGTTCAAGCGATT CAGGCGGGAGTGCAGTGGTGTGATCTCGGCTCGCTGCAACCTCCATTTTCCGAGTTCAAGCGATT T C AAK1 Ensembl:ENSG00000115977 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs777610060 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93707,RMVar_hsa_circ_109768,RMVar_hsa_circ_122881,RMVar_hsa_circ_268607,RMVar_hsa_circ_100894,RMVar_hsa_circ_200929,RMVar_hsa_circ_200931,RMVar_hsa_circ_200932,RMVar_hsa_circ_200930 45499 RMVar_ID_45499 Human_SNP_ID_76623195 A-to-I Human chr2 - 69462638 69462638 69462638 GGCGTCTTGCTCTGTCGCTCAGGCGGGAGTGCAGTGGTGTGATCTCGGCTCACTGCAACCTCCAT GGCGTCTTGCTCTGTCGCTCAGGCGGGAGTGCTGTGGTGTGATCTCGGCTCACTGCAACCTCCAT T A AAK1 Ensembl:ENSG00000115977 Protein coding 3'UTR GSE100210;GSE107867 HepG2 cell line;ASD brains,frontal_cortex - 29129909,30559470 RNA-Seq:(High) rs1218198177 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23881748 RMVar_hsa_circ_93707,RMVar_hsa_circ_109768,RMVar_hsa_circ_122881,RMVar_hsa_circ_268607,RMVar_hsa_circ_100894,RMVar_hsa_circ_200929,RMVar_hsa_circ_200931,RMVar_hsa_circ_200932,RMVar_hsa_circ_200930 45500 RMVar_ID_45500 Human_SNP_ID_76623491 A-to-I Human chr2 - 69463790 69463790 69463790 AATAAAAAAATAGGCTGGGCATGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGT AATAAAAAAATAGGCTGGGCATGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGT T C AAK1 Ensembl:ENSG00000115977 Protein coding 3'UTR GSE47997;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 23474544,31158229,31158229 RNA-Seq:(High) rs1005968675 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93707,RMVar_hsa_circ_109768,RMVar_hsa_circ_122881,RMVar_hsa_circ_268607,RMVar_hsa_circ_100894,RMVar_hsa_circ_200929,RMVar_hsa_circ_200931,RMVar_hsa_circ_200932,RMVar_hsa_circ_200930 45501 RMVar_ID_45501 Human_SNP_ID_76627745 A-to-I Human chr2 - 69482313 69482313 69482313 AGTTTCACTCTTGTTGCCTAGGCTGGAGTGCAATGGCAAGATCTCAGCTCACTGCAACCTCCATC AGTTTCACTCTTGTTGCCTAGGCTGGAGTGCAGTGGCAAGATCTCAGCTCACTGCAACCTCCATC T C AAK1 Ensembl:ENSG00000115977 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1416744172 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_26984,RMVar_hsa_circ_294699,RMVar_hsa_circ_200929,RMVar_hsa_circ_200931,RMVar_hsa_circ_200930,RMVar_hsa_circ_332877,RMVar_hsa_circ_371234,RMVar_hsa_circ_200933,RMVar_hsa_circ_38137 45502 RMVar_ID_45502 Human_SNP_ID_76633243 A-to-I Human chr2 - 69504200 69504200 69504200 TAGAGATGGAGTTTCACCATGTTGGCCATGCTAGTCTCGAACTCCTGAGCTCAAGTGATCTGCCT TAGAGATGGAGTTTCACCATGTTGGCCATGCTGGTCTCGAACTCCTGAGCTCAAGTGATCTGCCT T C AAK1 Ensembl:ENSG00000115977 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251259914 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 45503 RMVar_ID_45503 Human_SNP_ID_76635129 A-to-I Human chr2 - 69511720 69511720 69511720 CATCAACCTCGAGACAAAACAACTTCGGATGTAAAATGCCCTGGAGATTTCACCATCCCTTCCCT CATCAACCTCGAGACAAAACAACTTCGGATGTGAAATGCCCTGGAGATTTCACCATCCCTTCCCT T C AAK1 Ensembl:ENSG00000115977 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1489798324 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93707,RMVar_hsa_circ_109768,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_15045,RMVar_hsa_circ_200940,RMVar_hsa_circ_360735,RMVar_hsa_circ_65166,RMVar_hsa_circ_87009,RMVar_hsa_circ_200941,RMVar_hsa_circ_1258,RMVar_hsa_circ_117922,RMVar_hsa_circ_320132,RMVar_hsa_circ_200944,RMVar_hsa_circ_200945 45504 RMVar_ID_45504 Human_SNP_ID_76635133 A-to-I Human chr2 - 69511731 69511731 69511731 TTCCTTTATGCCATCAACCTCGAGACAAAACAACTTCGGATGTAAAATGCCCTGGAGATTTCACC TTCCTTTATGCCATCAACCTCGAGACAAAACAGCTTCGGATGTAAAATGCCCTGGAGATTTCACC T C AAK1 Ensembl:ENSG00000115977 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1246915872 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93707,RMVar_hsa_circ_109768,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_15045,RMVar_hsa_circ_200940,RMVar_hsa_circ_360735,RMVar_hsa_circ_65166,RMVar_hsa_circ_87009,RMVar_hsa_circ_200941,RMVar_hsa_circ_1258,RMVar_hsa_circ_117922,RMVar_hsa_circ_320132,RMVar_hsa_circ_200944,RMVar_hsa_circ_200945 45505 RMVar_ID_45505 Human_SNP_ID_76635141 A-to-I Human chr2 - 69511769 69511769 69511769 AAATGTTCTCCAAGTGGTAAGAAAACTATCCAACTCCTTTCCTTTATGCCATCAACCTCGAGACA AAATGTTCTCCAAGTGGTAAGAAAACTATCCAGCTCCTTTCCTTTATGCCATCAACCTCGAGACA T C AAK1 Ensembl:ENSG00000115977 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1365277361 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93707,RMVar_hsa_circ_109768,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_15045,RMVar_hsa_circ_200940,RMVar_hsa_circ_360735,RMVar_hsa_circ_65166,RMVar_hsa_circ_87009,RMVar_hsa_circ_200941,RMVar_hsa_circ_1258,RMVar_hsa_circ_117922,RMVar_hsa_circ_320132,RMVar_hsa_circ_200944,RMVar_hsa_circ_200945 45506 RMVar_ID_45506 Human_SNP_ID_76635144 A-to-I Human chr2 - 69511777 69511777 69511777 GAAGAGAAAAATGTTCTCCAAGTGGTAAGAAAACTATCCAACTCCTTTCCTTTATGCCATCAACC GAAGAGAAAAATGTTCTCCAAGTGGTAAGAAAGCTATCCAACTCCTTTCCTTTATGCCATCAACC T C AAK1 Ensembl:ENSG00000115977 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1415472691 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93707,RMVar_hsa_circ_109768,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_15045,RMVar_hsa_circ_200940,RMVar_hsa_circ_360735,RMVar_hsa_circ_65166,RMVar_hsa_circ_87009,RMVar_hsa_circ_200941,RMVar_hsa_circ_1258,RMVar_hsa_circ_117922,RMVar_hsa_circ_320132,RMVar_hsa_circ_200944,RMVar_hsa_circ_200945 45507 RMVar_ID_45507 Human_SNP_ID_76661893 A-to-I Human chr2 - 69626640 69626640 69626640 AAAAAAAAAGCCAGGCATGGTGGAATGCACCTATAGTCCCACCTACTTAGGAGGCTGAGGTGGGA AAAAAAAAAGCCAGGCATGGTGGAATGCACCTGTAGTCCCACCTACTTAGGAGGCTGAGGTGGGA T C AAK1 Ensembl:ENSG00000115977 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965997194 Functional Loss SNV dbSNP153 33..33 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 45508 RMVar_ID_45508 Human_SNP_ID_76667163 A-to-I Human chr2 + 69647809 69647809 69647809 AAACTCCTGGACTCAGGTGATCCTCCCACCTCAGCCTCCCAAAGTGCTGAGATTACAGATGTGAG AAACTCCTGGACTCAGGTGATCCTCCCACCTCCGCCTCCCAAAGTGCTGAGATTACAGATGTGAG A C ANXA4 Ensembl:ENSG00000196975 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1220825968 Functional Loss SNV dbSNP153 33..33 33 - - - 45509 RMVar_ID_45509 Human_SNP_ID_76671575 A-to-I Human chr2 + 69663561 69663561 69663561 ACAAGACTGTAGTCCCTGCTTCTCCACAGGCTAAGGTAGGAGGATTGCTTGAGCCCAGTTTGAGG ACAAGACTGTAGTCCCTGCTTCTCCACAGGCTGAGGTAGGAGGATTGCTTGAGCCCAGTTTGAGG A G ANXA4 Ensembl:ENSG00000196975 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1383379995 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39892 45510 RMVar_ID_45510 Human_SNP_ID_76689642 A-to-I Human chr2 + 69743169 69743169 69743169 CTGAGACTACAGGTGCATGCCACCACGTGCCTATAGTCTCAGCTATTCAGGAGGTAACTGGTAAC CTGAGACTACAGGTGCATGCCACCACGTGCCTGTAGTCTCAGCTATTCAGGAGGTAACTGGTAAC A G ANXA4 Ensembl:ENSG00000196975 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs867602845 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_200954,RMVar_hsa_circ_82261 45511 RMVar_ID_45511 Human_SNP_ID_76693347 A-to-I Human chr2 + 69759042 69759042 69759042 CCTGTAATCCCAGCTACTCAGGAGGCTGGGGCAAGAGAATCCCTTGAACACGGGAGGCGGAGGTT CCTGTAATCCCAGCTACTCAGGAGGCTGGGGCCAGAGAATCCCTTGAACACGGGAGGCGGAGGTT A C ANXA4 Ensembl:ENSG00000196975 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1184727711 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_200954,RMVar_hsa_circ_82261 45512 RMVar_ID_45512 Human_SNP_ID_76710361 A-to-I Human chr2 + 69831458 69831458 69831458 TTTTTGGAGCTTTTTTCTAAAGGAGTCTCACTATATTGCCCAGGCTGGTCTCAAACGCCTGGGTT TTTTTGGAGCTTTTTTCTAAAGGAGTCTCACTCTATTGCCCAGGCTGGTCTCAAACGCCTGGGTT A C GMCL1 Ensembl:ENSG00000087338 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs368758930 Functional Loss SNV dbSNP153 33..33 33 - - - 45513 RMVar_ID_45513 Human_SNP_ID_76710362 A-to-I Human chr2 + 69831458 69831458 69831458 TTTTTGGAGCTTTTTTCTAAAGGAGTCTCACTATATTGCCCAGGCTGGTCTCAAACGCCTGGGTT TTTTTGGAGCTTTTTTCTAAAGGAGTCTCACTGTATTGCCCAGGCTGGTCTCAAACGCCTGGGTT A G GMCL1 Ensembl:ENSG00000087338 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs368758930 Functional Loss SNV dbSNP153 33..33 33 - - - 45514 RMVar_ID_45514 Human_SNP_ID_76710450 A-to-I Human chr2 + 69831793 69831793 69831793 CACACCCAGCTAATTTTTTTATTTGTAGAAACAAGGTCTCACTCTGTTGCCCACCCAGGCTGGCC CACACCCAGCTAATTTTTTTATTTGTAGAAACGAGGTCTCACTCTGTTGCCCACCCAGGCTGGCC A G GMCL1 Ensembl:ENSG00000087338 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs564672842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13947492 45515 RMVar_ID_45515 Human_SNP_ID_76710487 A-to-I Human chr2 + 69831963 69831963 69831963 GAGTTCTTGGCCAGGTGCAGTGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCTGAAGCAGAC GAGTTCTTGGCCAGGTGCAGTGGCTCATGCCTCTAATCCCAGCACTTTGGGAGGCTGAAGCAGAC A C GMCL1 Ensembl:ENSG00000087338 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs528846158 Functional Loss SNV dbSNP153 33..33 33 - - - 45516 RMVar_ID_45516 Human_SNP_ID_76710488 A-to-I Human chr2 + 69831963 69831963 69831963 GAGTTCTTGGCCAGGTGCAGTGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCTGAAGCAGAC GAGTTCTTGGCCAGGTGCAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAAGCAGAC A G GMCL1 Ensembl:ENSG00000087338 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs528846158 Functional Loss SNV dbSNP153 33..33 33 - - - 45517 RMVar_ID_45517 Human_SNP_ID_76729155 A-to-I Human chr2 + 69909891 69909891 69909891 ATTGCTTGAACCCAGGAGGCGGAGGTTGCAGTAAGCAGAGATTGCACCATTGCACTCCAGCCTGG ATTGCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCAGAGATTGCACCATTGCACTCCAGCCTGG A G MXD1 Ensembl:ENSG00000059728 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1558564653 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25560704 45518 RMVar_ID_45518 Human_SNP_ID_76755728 A-to-I Human chr2 - 70014550 70014550 70014550 GTGATTTGTCTGCCTCAGCCTCCCAAAGTGTTAGGATTACAGGTGTGAGCCACTGCACCCGGCTG GTGATTTGTCTGCCTCAGCCTCCCAAAGTGTTGGGATTACAGGTGTGAGCCACTGCACCCGGCTG T C PCBP1-AS1 Ensembl:ENSG00000179818 lincRNA intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1246474453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_256756 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_200985,RMVar_hsa_circ_200986 45519 RMVar_ID_45519 Human_SNP_ID_76756272 A-to-I Human chr2 - 70016651 70016651 70016651 TCAGTAGAGATGGGTCTTCACCATGTTGGCCAAGCTGCTCTCAAACTCCTGACCTCAAGTCTGCC TCAGTAGAGATGGGTCTTCACCATGTTGGCCAGGCTGCTCTCAAACTCCTGACCTCAAGTCTGCC T C PCBP1-AS1 Ensembl:ENSG00000179818 lincRNA intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1419296734 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3412,RMVar_hsa_circ_4517,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_200985,RMVar_hsa_circ_200986 45520 RMVar_ID_45520 Human_SNP_ID_76758810 A-to-I Human chr2 - 70026139 70026139 70026139 AATTTTTGTATTTTTAGTAGAGACAAGGTTTCACCATGTTAGGCTGGTCTTGAACTCCTGACCTC AATTTTTGTATTTTTAGTAGAGACAAGGTTTCGCCATGTTAGGCTGGTCTTGAACTCCTGACCTC T C PCBP1-AS1 Ensembl:ENSG00000179818 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1347246617 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3412,RMVar_hsa_circ_4517,RMVar_hsa_circ_307543,RMVar_hsa_circ_15393,RMVar_hsa_circ_200980,RMVar_hsa_circ_350095,RMVar_hsa_circ_200983,RMVar_hsa_circ_273703,RMVar_hsa_circ_295559,RMVar_hsa_circ_313424,RMVar_hsa_circ_353157,RMVar_hsa_circ_200985,RMVar_hsa_circ_200986 45521 RMVar_ID_45521 Human_SNP_ID_76760309 A-to-I Human chr2 - 70031656 70031656 70031656 GTCTTGCTCTGTCGCCCAGGCTGGAGTGCAGTAGCTCAATCTCGGCTCACTGCAAGCTCCACCTC GTCTTGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCTCAATCTCGGCTCACTGCAAGCTCCACCTC T C PCBP1-AS1 Ensembl:ENSG00000179818 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1201133942 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25560835 RMVar_hsa_circ_3412,RMVar_hsa_circ_4517,RMVar_hsa_circ_307543,RMVar_hsa_circ_15393,RMVar_hsa_circ_200980,RMVar_hsa_circ_350095,RMVar_hsa_circ_200983,RMVar_hsa_circ_273703,RMVar_hsa_circ_295559,RMVar_hsa_circ_313424,RMVar_hsa_circ_353157,RMVar_hsa_circ_200985,RMVar_hsa_circ_200986,RMVar_hsa_circ_200987,RMVar_hsa_circ_114923 45522 RMVar_ID_45522 Human_SNP_ID_76761674 A-to-I Human chr2 - 70036546 70036546 70036546 CTTCCAATTTTGGTGTAGACAAACACCTTGGCATTATCAGTGACTTGTTACTCTGTTCTCCTCTT CTTCCAATTTTGGTGTAGACAAACACCTTGGCGTTATCAGTGACTTGTTACTCTGTTCTCCTCTT T C PCBP1-AS1 Ensembl:ENSG00000179818 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1307360183 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3412,RMVar_hsa_circ_4517,RMVar_hsa_circ_307543,RMVar_hsa_circ_15393,RMVar_hsa_circ_200980,RMVar_hsa_circ_350095,RMVar_hsa_circ_200983,RMVar_hsa_circ_295559,RMVar_hsa_circ_313424,RMVar_hsa_circ_353157,RMVar_hsa_circ_200986,RMVar_hsa_circ_200988,RMVar_hsa_circ_313048,RMVar_hsa_circ_349854 45523 RMVar_ID_45523 Human_SNP_ID_76761874 A-to-I Human chr2 - 70037273 70037273 70037273 TTGCTTGAGCTCAGGAGTTTGAGAACAGACTAACAAGTCACTGATTATGCCAAGGTGTTTATCTA TTGCTTGAGCTCAGGAGTTTGAGAACAGACTAGCAAGTCACTGATTATGCCAAGGTGTTTATCTA T C PCBP1-AS1 Ensembl:ENSG00000179818 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs915504728 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6944276 RMVar_hsa_circ_3412,RMVar_hsa_circ_4517,RMVar_hsa_circ_307543,RMVar_hsa_circ_15393,RMVar_hsa_circ_200980,RMVar_hsa_circ_350095,RMVar_hsa_circ_200983,RMVar_hsa_circ_295559,RMVar_hsa_circ_313424,RMVar_hsa_circ_353157,RMVar_hsa_circ_200986,RMVar_hsa_circ_200988,RMVar_hsa_circ_313048,RMVar_hsa_circ_349854 45524 RMVar_ID_45524 Human_SNP_ID_76762737 A-to-I Human chr2 - 70040292 70040292 70040292 ACAGTTCACTGCAGCTTCAAACTTCTGAGCTCAAGCAATCTTCCTGTCTCAGCCTCCCTGAGTAG ACAGTTCACTGCAGCTTCAAACTTCTGAGCTCTAGCAATCTTCCTGTCTCAGCCTCCCTGAGTAG T A PCBP1-AS1 Ensembl:ENSG00000179818 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1484333917 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3412,RMVar_hsa_circ_4517,RMVar_hsa_circ_307543,RMVar_hsa_circ_15393,RMVar_hsa_circ_200980,RMVar_hsa_circ_350095,RMVar_hsa_circ_200983,RMVar_hsa_circ_295559,RMVar_hsa_circ_313424,RMVar_hsa_circ_353157,RMVar_hsa_circ_200986,RMVar_hsa_circ_200988,RMVar_hsa_circ_313048,RMVar_hsa_circ_349854 45525 RMVar_ID_45525 Human_SNP_ID_76763944 A-to-I Human chr2 - 70044571 70044571 70044571 CCTGTGATCCCAGCCACTTGGGAGGCTGTGGCAGGAGAATCGCCTGAATCCGCGAGGCGGTGGTT CCTGTGATCCCAGCCACTTGGGAGGCTGTGGCGGGAGAATCGCCTGAATCCGCGAGGCGGTGGTT T C PCBP1-AS1 Ensembl:ENSG00000179818 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1425824509 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3412,RMVar_hsa_circ_4517,RMVar_hsa_circ_307543,RMVar_hsa_circ_15393,RMVar_hsa_circ_200980,RMVar_hsa_circ_350095,RMVar_hsa_circ_200983,RMVar_hsa_circ_295559,RMVar_hsa_circ_313424,RMVar_hsa_circ_353157,RMVar_hsa_circ_200986,RMVar_hsa_circ_200988,RMVar_hsa_circ_313048,RMVar_hsa_circ_349854 45526 RMVar_ID_45526 Human_SNP_ID_76767585 A-to-I Human chr2 - 70056872 70056872 70056872 AAATTAGCTGGGTGAGGTGGCGCACGCCTGTAATCCCAGCTACTCGCGAGGCTGAGACGGGAGAA AAATTAGCTGGGTGAGGTGGCGCACGCCTGTAGTCCCAGCTACTCGCGAGGCTGAGACGGGAGAA T C PCBP1-AS1 Ensembl:ENSG00000179818 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1207000766 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21594,RMVar_hsa_circ_15393,RMVar_hsa_circ_200980,RMVar_hsa_circ_350095,RMVar_hsa_circ_313424,RMVar_hsa_circ_282110,RMVar_hsa_circ_200988,RMVar_hsa_circ_313048,RMVar_hsa_circ_275476,RMVar_hsa_circ_200990,RMVar_hsa_circ_71384,RMVar_hsa_circ_307122 45527 RMVar_ID_45527 Human_SNP_ID_76767846 A-to-I Human chr2 - 70057754 70057754 70057754 GTTTTACTGGCTGGGCGCAGTGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCCGAGGCGGGT GTTTTACTGGCTGGGCGCAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGT T C PCBP1-AS1 Ensembl:ENSG00000179818 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049589564 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21594,RMVar_hsa_circ_15393,RMVar_hsa_circ_200980,RMVar_hsa_circ_350095,RMVar_hsa_circ_313424,RMVar_hsa_circ_282110,RMVar_hsa_circ_200988,RMVar_hsa_circ_313048,RMVar_hsa_circ_275476,RMVar_hsa_circ_200990,RMVar_hsa_circ_71384,RMVar_hsa_circ_307122 45528 RMVar_ID_45528 Human_SNP_ID_76772136 A-to-I Human chr2 - 70071685 70071685 70071685 CAGGCTGGAGTGCAGTGGCACGATATCGGCTCACTGCAACCTCCACCTCCTGGGTTCAAGTGATT CAGGCTGGAGTGCAGTGGCACGATATCGGCTCCCTGCAACCTCCACCTCCTGGGTTCAAGTGATT T G PCBP1-AS1 Ensembl:ENSG00000179818 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569893428 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_256519 RMVar_hsa_circ_21594,RMVar_hsa_circ_15393,RMVar_hsa_circ_200980,RMVar_hsa_circ_350095,RMVar_hsa_circ_313424,RMVar_hsa_circ_282110,RMVar_hsa_circ_200988,RMVar_hsa_circ_313048,RMVar_hsa_circ_275476,RMVar_hsa_circ_200990,RMVar_hsa_circ_71384,RMVar_hsa_circ_307122,RMVar_hsa_circ_200991,RMVar_hsa_circ_109530 45529 RMVar_ID_45529 Human_SNP_ID_76772295 A-to-I Human chr2 - 70072231 70072231 70072231 ATTTTCTGTAGAGGCTGGGTGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGT ATTTTCTGTAGAGGCTGGGTGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGT T C PCBP1-AS1 Ensembl:ENSG00000179818 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1036458305 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21594,RMVar_hsa_circ_15393,RMVar_hsa_circ_200980,RMVar_hsa_circ_350095,RMVar_hsa_circ_313424,RMVar_hsa_circ_282110,RMVar_hsa_circ_200988,RMVar_hsa_circ_313048,RMVar_hsa_circ_275476,RMVar_hsa_circ_200990,RMVar_hsa_circ_71384,RMVar_hsa_circ_307122,RMVar_hsa_circ_200991,RMVar_hsa_circ_109530 45530 RMVar_ID_45530 Human_SNP_ID_76772296 A-to-I Human chr2 - 70072231 70072231 70072231 ATTTTCTGTAGAGGCTGGGTGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGT ATTTTCTGTAGAGGCTGGGTGCAGTGGCTCACCCCTGTAATCCCAGCACTTTGGGAGGCCGAGGT T G PCBP1-AS1 Ensembl:ENSG00000179818 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1036458305 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21594,RMVar_hsa_circ_15393,RMVar_hsa_circ_200980,RMVar_hsa_circ_350095,RMVar_hsa_circ_313424,RMVar_hsa_circ_282110,RMVar_hsa_circ_200988,RMVar_hsa_circ_313048,RMVar_hsa_circ_275476,RMVar_hsa_circ_200990,RMVar_hsa_circ_71384,RMVar_hsa_circ_307122,RMVar_hsa_circ_200991,RMVar_hsa_circ_109530 45531 RMVar_ID_45531 Human_SNP_ID_76774519 A-to-I Human chr2 - 70079421 70079421 70079421 TTGTCCAGGCCGGACTGCAGTGGCATGATAATAGTTGACTGTAGCCTTGAATTCCTGGTCTCAAG TTGTCCAGGCCGGACTGCAGTGGCATGATAATTGTTGACTGTAGCCTTGAATTCCTGGTCTCAAG T A PCBP1-AS1 Ensembl:ENSG00000179818 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1273794787 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13949181 RMVar_hsa_circ_21594,RMVar_hsa_circ_15393,RMVar_hsa_circ_200980,RMVar_hsa_circ_350095,RMVar_hsa_circ_313424,RMVar_hsa_circ_282110,RMVar_hsa_circ_200988,RMVar_hsa_circ_313048,RMVar_hsa_circ_275476,RMVar_hsa_circ_200990,RMVar_hsa_circ_307122,RMVar_hsa_circ_200991,RMVar_hsa_circ_109530,RMVar_hsa_circ_284407 45532 RMVar_ID_45532 Human_SNP_ID_76777897 A-to-I Human chr2 + 70088559 70088559 70088559 TCCAGCTCTCCAGAGGTGAAAGGCTATTGGGCAAGTTTGGATGCATCTACTCAAACCACCCATGA TCCAGCTCTCCAGAGGTGAAAGGCTATTGGGCGAGTTTGGATGCATCTACTCAAACCACCCATGA A G PCBP1 Ensembl:ENSG00000169564 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs777725053 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_554587,Human_RBP_ID_1589450,Human_RBP_ID_1922360,Human_RBP_ID_6944400,Human_RBP_ID_8524107,Human_RBP_ID_13949309,Human_RBP_ID_18318659,Human_RBP_ID_22394061,Human_RBP_ID_23882233 45533 RMVar_ID_45533 Human_SNP_ID_76804560 A-to-I Human chr2 - 70189241 70189241 70189241 TCACCACGCCCGGCTAATTTTGTATTTTTAGTAGAGATAGGGTTTCTCCATGTTGTTCAGGCTGG TCACCACGCCCGGCTAATTTTGTATTTTTAGTTGAGATAGGGTTTCTCCATGTTGTTCAGGCTGG T A C2orf42 Ensembl:ENSG00000115998 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1224569765 Functional Loss SNV dbSNP153 33..33 33 - - - 45534 RMVar_ID_45534 Human_SNP_ID_76806176 A-to-I Human chr2 - 70194329 70194329 70194329 GGAGTGCAGTGGTGCGATCTTGGCTCACTGCAACCTCTGCCTCCCGGGTTCAGGCGATTCTTCTG GGAGTGCAGTGGTGCGATCTTGGCTCACTGCAGCCTCTGCCTCCCGGGTTCAGGCGATTCTTCTG T C C2orf42 Ensembl:ENSG00000115998 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs542722724 Functional Loss SNV dbSNP153 33..33 33 - - - 45535 RMVar_ID_45535 Human_SNP_ID_76808960 A-to-I Human chr2 - 70204998 70204998 70204998 GATTCTCAAGCCAGGCGCAGTGGCTCAGGCCTATAACTCCCACACTTTAGGAGGCCAAGGCAGAA GATTCTCAAGCCAGGCGCAGTGGCTCAGGCCTGTAACTCCCACACTTTAGGAGGCCAAGGCAGAA T C C2orf42 Ensembl:ENSG00000115998 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs115940067 Functional Loss SNV dbSNP153 33..33 33 - - - 45536 RMVar_ID_45536 Human_SNP_ID_76809922 A-to-I Human chr2 - 70207708 70207708 70207708 TCTACTAAAAATACAAAAAATCCCAGCTGCTCAGGCGGCTGAGGTGGGAGAATTGCTTGAACCTG TCTACTAAAAATACAAAAAATCCCAGCTGCTCCGGCGGCTGAGGTGGGAGAATTGCTTGAACCTG T G C2orf42 Ensembl:ENSG00000115998 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1385080975 Functional Loss SNV dbSNP153 33..33 33 - - - 45537 RMVar_ID_45537 Human_SNP_ID_76813150 A-to-I Human chr2 - 70219549 70219549 70219549 GAGTATCACTTGAGCCCAAGGAGTTCAAGGCTACAGTAAGCTGTGATCATGCCTGGATGACAGAA GAGTATCACTTGAGCCCAAGGAGTTCAAGGCTGCAGTAAGCTGTGATCATGCCTGGATGACAGAA T C TIA1,C2orf42 Ensembl:ENSG00000116001,Ensembl:ENSG00000115998 Protein coding,Protein coding intron,intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1167578159 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6547,RMVar_hsa_circ_343601,RMVar_hsa_circ_299907,RMVar_hsa_circ_300794,RMVar_hsa_circ_201007,RMVar_hsa_circ_201008,RMVar_hsa_circ_201009,RMVar_hsa_circ_201010,RMVar_hsa_circ_360251,RMVar_hsa_circ_361415,RMVar_hsa_circ_48873,RMVar_hsa_circ_288024,RMVar_hsa_circ_305978,RMVar_hsa_circ_65868,RMVar_hsa_circ_37948,RMVar_hsa_circ_201012,RMVar_hsa_circ_201011,RMVar_hsa_circ_291604,RMVar_hsa_circ_55380 45538 RMVar_ID_45538 Human_SNP_ID_76813168 A-to-I Human chr2 - 70219599 70219599 70219599 AACCTTGTTGGTGCATGCTTATAGTCCTAGCTACTAGGAGGCTGAGGTGGGAGTATCACTTGAGC AACCTTGTTGGTGCATGCTTATAGTCCTAGCTGCTAGGAGGCTGAGGTGGGAGTATCACTTGAGC T C TIA1,C2orf42 Ensembl:ENSG00000116001,Ensembl:ENSG00000115998 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1401285125 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13949797,Human_RBP_ID_22598294 RMVar_hsa_circ_6547,RMVar_hsa_circ_343601,RMVar_hsa_circ_299907,RMVar_hsa_circ_300794,RMVar_hsa_circ_201007,RMVar_hsa_circ_201008,RMVar_hsa_circ_201009,RMVar_hsa_circ_201010,RMVar_hsa_circ_360251,RMVar_hsa_circ_361415,RMVar_hsa_circ_48873,RMVar_hsa_circ_288024,RMVar_hsa_circ_305978,RMVar_hsa_circ_65868,RMVar_hsa_circ_37948,RMVar_hsa_circ_201012,RMVar_hsa_circ_201011,RMVar_hsa_circ_291604,RMVar_hsa_circ_55380 45539 RMVar_ID_45539 Human_SNP_ID_76813259 A-to-I Human chr2 - 70219852 70219852 70219852 TTTCCTGCCAGGCACAGTGGCTCATTCCTGTAATAACAGAACTTTGGGAGGCCAAGGCAGGAGGA TTTCCTGCCAGGCACAGTGGCTCATTCCTGTAGTAACAGAACTTTGGGAGGCCAAGGCAGGAGGA T C TIA1,C2orf42 Ensembl:ENSG00000116001,Ensembl:ENSG00000115998 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1134459 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13949806,Human_RBP_ID_20594266 RMVar_hsa_circ_6547,RMVar_hsa_circ_343601,RMVar_hsa_circ_299907,RMVar_hsa_circ_300794,RMVar_hsa_circ_201007,RMVar_hsa_circ_201008,RMVar_hsa_circ_201009,RMVar_hsa_circ_201010,RMVar_hsa_circ_360251,RMVar_hsa_circ_361415,RMVar_hsa_circ_48873,RMVar_hsa_circ_288024,RMVar_hsa_circ_305978,RMVar_hsa_circ_65868,RMVar_hsa_circ_37948,RMVar_hsa_circ_201012,RMVar_hsa_circ_201011,RMVar_hsa_circ_291604,RMVar_hsa_circ_55380 45540 RMVar_ID_45540 Human_SNP_ID_76813266 A-to-I Human chr2 - 70219869 70219869 70219869 CTTTTTAAGAATGTGCATTTCCTGCCAGGCACAGTGGCTCATTCCTGTAATAACAGAACTTTGGG CTTTTTAAGAATGTGCATTTCCTGCCAGGCACGGTGGCTCATTCCTGTAATAACAGAACTTTGGG T C TIA1,C2orf42 Ensembl:ENSG00000116001,Ensembl:ENSG00000115998 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1033717941 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6547,RMVar_hsa_circ_343601,RMVar_hsa_circ_299907,RMVar_hsa_circ_300794,RMVar_hsa_circ_201007,RMVar_hsa_circ_201008,RMVar_hsa_circ_201009,RMVar_hsa_circ_201010,RMVar_hsa_circ_360251,RMVar_hsa_circ_361415,RMVar_hsa_circ_48873,RMVar_hsa_circ_288024,RMVar_hsa_circ_305978,RMVar_hsa_circ_65868,RMVar_hsa_circ_37948,RMVar_hsa_circ_201012,RMVar_hsa_circ_201011,RMVar_hsa_circ_291604,RMVar_hsa_circ_55380 45541 RMVar_ID_45541 Human_SNP_ID_76813394 A-to-I Human chr2 - 70220357 70220357 70220357 TCACCCAGGCTGGAGTGTGGTGGCACAATCACAACTCACTGCAGCCTTGACCTCCCAGGCTTAGG TCACCCAGGCTGGAGTGTGGTGGCACAATCACCACTCACTGCAGCCTTGACCTCCCAGGCTTAGG T G TIA1,C2orf42 Ensembl:ENSG00000116001,Ensembl:ENSG00000115998 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs995607020 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13949825,Human_RBP_ID_25591267 RMVar_hsa_circ_6547,RMVar_hsa_circ_343601,RMVar_hsa_circ_299907,RMVar_hsa_circ_300794,RMVar_hsa_circ_201007,RMVar_hsa_circ_201008,RMVar_hsa_circ_201009,RMVar_hsa_circ_201010,RMVar_hsa_circ_360251,RMVar_hsa_circ_361415,RMVar_hsa_circ_48873,RMVar_hsa_circ_288024,RMVar_hsa_circ_305978,RMVar_hsa_circ_65868,RMVar_hsa_circ_37948,RMVar_hsa_circ_201012,RMVar_hsa_circ_201011,RMVar_hsa_circ_291604,RMVar_hsa_circ_55380 45542 RMVar_ID_45542 Human_SNP_ID_76813396 A-to-I Human chr2 - 70220365 70220365 70220365 TCACTCTGTCACCCAGGCTGGAGTGTGGTGGCACAATCACAACTCACTGCAGCCTTGACCTCCCA TCACTCTGTCACCCAGGCTGGAGTGTGGTGGCGCAATCACAACTCACTGCAGCCTTGACCTCCCA T C TIA1,C2orf42 Ensembl:ENSG00000116001,Ensembl:ENSG00000115998 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048668954 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_242626,Human_RBP_ID_25591267 RMVar_hsa_circ_6547,RMVar_hsa_circ_343601,RMVar_hsa_circ_299907,RMVar_hsa_circ_300794,RMVar_hsa_circ_201007,RMVar_hsa_circ_201008,RMVar_hsa_circ_201009,RMVar_hsa_circ_201010,RMVar_hsa_circ_360251,RMVar_hsa_circ_361415,RMVar_hsa_circ_48873,RMVar_hsa_circ_288024,RMVar_hsa_circ_305978,RMVar_hsa_circ_65868,RMVar_hsa_circ_37948,RMVar_hsa_circ_201012,RMVar_hsa_circ_201011,RMVar_hsa_circ_291604,RMVar_hsa_circ_55380 45543 RMVar_ID_45543 Human_SNP_ID_76813599 A-to-I Human chr2 - 70221118 70221118 70221118 CCTGTAATCACGGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACCTGGGAGGCAAAGGTT CCTGTAATCACGGCTACTCAGGAGGCTGAGGCCGGAGAATCGCTTGAACCTGGGAGGCAAAGGTT T G TIA1,C2orf42 Ensembl:ENSG00000116001,Ensembl:ENSG00000115998 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1276919299 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6547,RMVar_hsa_circ_343601,RMVar_hsa_circ_299907,RMVar_hsa_circ_300794,RMVar_hsa_circ_201007,RMVar_hsa_circ_201008,RMVar_hsa_circ_201009,RMVar_hsa_circ_201010,RMVar_hsa_circ_360251,RMVar_hsa_circ_361415,RMVar_hsa_circ_48873,RMVar_hsa_circ_288024,RMVar_hsa_circ_305978,RMVar_hsa_circ_65868,RMVar_hsa_circ_37948,RMVar_hsa_circ_201012,RMVar_hsa_circ_201011,RMVar_hsa_circ_291604,RMVar_hsa_circ_55380 45544 RMVar_ID_45544 Human_SNP_ID_76813645 A-to-I Human chr2 - 70221278 70221278 70221278 AAAAAAGGCCAGGCATGGTGGCTCACACTTGTAATCCCAGCACTTTGGGTGGCCGAGGCAAGCAG AAAAAAGGCCAGGCATGGTGGCTCACACTTGTGATCCCAGCACTTTGGGTGGCCGAGGCAAGCAG T C TIA1,C2orf42 Ensembl:ENSG00000116001,Ensembl:ENSG00000115998 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1355777678 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569731 RMVar_hsa_circ_6547,RMVar_hsa_circ_343601,RMVar_hsa_circ_299907,RMVar_hsa_circ_300794,RMVar_hsa_circ_201007,RMVar_hsa_circ_201008,RMVar_hsa_circ_201009,RMVar_hsa_circ_201010,RMVar_hsa_circ_360251,RMVar_hsa_circ_361415,RMVar_hsa_circ_48873,RMVar_hsa_circ_288024,RMVar_hsa_circ_305978,RMVar_hsa_circ_65868,RMVar_hsa_circ_37948,RMVar_hsa_circ_201012,RMVar_hsa_circ_201011,RMVar_hsa_circ_291604,RMVar_hsa_circ_55380 45545 RMVar_ID_45545 Human_SNP_ID_76814356 A-to-I Human chr2 - 70223851 70223851 70223851 TAAATATTACCCGGGCACAGTGGTTTATGCCTATAACCTCAGCACTTTGGGAGGCTGAGAAGTTT TAAATATTACCCGGGCACAGTGGTTTATGCCTGTAACCTCAGCACTTTGGGAGGCTGAGAAGTTT T C TIA1,C2orf42 Ensembl:ENSG00000116001,Ensembl:ENSG00000115998 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs967909297 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25561322 RMVar_hsa_circ_6547,RMVar_hsa_circ_343601,RMVar_hsa_circ_299907,RMVar_hsa_circ_300794,RMVar_hsa_circ_201007,RMVar_hsa_circ_201008,RMVar_hsa_circ_201009,RMVar_hsa_circ_201010,RMVar_hsa_circ_360251,RMVar_hsa_circ_361415,RMVar_hsa_circ_48873,RMVar_hsa_circ_288024,RMVar_hsa_circ_305978,RMVar_hsa_circ_65868,RMVar_hsa_circ_37948,RMVar_hsa_circ_201012,RMVar_hsa_circ_201011,RMVar_hsa_circ_291604,RMVar_hsa_circ_55380 45546 RMVar_ID_45546 Human_SNP_ID_76814430 A-to-I Human chr2 - 70224091 70224091 70224091 CAACCTGGTGAAACCCTGTTTCTACTAAAAATACAAAAATTATCCGGGCGTGGTGGCAGGCGCCT CAACCTGGTGAAACCCTGTTTCTACTAAAAATGCAAAAATTATCCGGGCGTGGTGGCAGGCGCCT T C TIA1,C2orf42 Ensembl:ENSG00000116001,Ensembl:ENSG00000115998 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1280376194 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25591283 RMVar_hsa_circ_6547,RMVar_hsa_circ_343601,RMVar_hsa_circ_299907,RMVar_hsa_circ_300794,RMVar_hsa_circ_201007,RMVar_hsa_circ_201008,RMVar_hsa_circ_201009,RMVar_hsa_circ_201010,RMVar_hsa_circ_360251,RMVar_hsa_circ_361415,RMVar_hsa_circ_48873,RMVar_hsa_circ_288024,RMVar_hsa_circ_305978,RMVar_hsa_circ_65868,RMVar_hsa_circ_37948,RMVar_hsa_circ_201012,RMVar_hsa_circ_201011,RMVar_hsa_circ_291604,RMVar_hsa_circ_55380 45547 RMVar_ID_45547 Human_SNP_ID_76814435 A-to-I Human chr2 - 70224121 70224121 70224121 CTGAGGTCAGGACTTTGAGAACAGCCAGGTCAACCTGGTGAAACCCTGTTTCTACTAAAAATACA CTGAGGTCAGGACTTTGAGAACAGCCAGGTCAGCCTGGTGAAACCCTGTTTCTACTAAAAATACA T C TIA1,C2orf42 Ensembl:ENSG00000116001,Ensembl:ENSG00000115998 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs961391024 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6944623,Human_RBP_ID_13949958 RMVar_hsa_circ_6547,RMVar_hsa_circ_343601,RMVar_hsa_circ_299907,RMVar_hsa_circ_300794,RMVar_hsa_circ_201007,RMVar_hsa_circ_201008,RMVar_hsa_circ_201009,RMVar_hsa_circ_201010,RMVar_hsa_circ_360251,RMVar_hsa_circ_361415,RMVar_hsa_circ_48873,RMVar_hsa_circ_288024,RMVar_hsa_circ_305978,RMVar_hsa_circ_65868,RMVar_hsa_circ_37948,RMVar_hsa_circ_201012,RMVar_hsa_circ_201011,RMVar_hsa_circ_291604,RMVar_hsa_circ_55380 45548 RMVar_ID_45548 Human_SNP_ID_76814436 A-to-I Human chr2 - 70224121 70224121 70224121 CTGAGGTCAGGACTTTGAGAACAGCCAGGTCAACCTGGTGAAACCCTGTTTCTACTAAAAATACA CTGAGGTCAGGACTTTGAGAACAGCCAGGTCACCCTGGTGAAACCCTGTTTCTACTAAAAATACA T G TIA1,C2orf42 Ensembl:ENSG00000116001,Ensembl:ENSG00000115998 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs961391024 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6944623,Human_RBP_ID_13949958 RMVar_hsa_circ_6547,RMVar_hsa_circ_343601,RMVar_hsa_circ_299907,RMVar_hsa_circ_300794,RMVar_hsa_circ_201007,RMVar_hsa_circ_201008,RMVar_hsa_circ_201009,RMVar_hsa_circ_201010,RMVar_hsa_circ_360251,RMVar_hsa_circ_361415,RMVar_hsa_circ_48873,RMVar_hsa_circ_288024,RMVar_hsa_circ_305978,RMVar_hsa_circ_65868,RMVar_hsa_circ_37948,RMVar_hsa_circ_201012,RMVar_hsa_circ_201011,RMVar_hsa_circ_291604,RMVar_hsa_circ_55380 45549 RMVar_ID_45549 Human_SNP_ID_76814451 A-to-I Human chr2 - 70224184 70224184 70224184 GCCGGACGCAGTGGCTCACACCTGTAATCCCAACACTTTGGGAGGCTGAGGCGGGTGGATCACCT GCCGGACGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGTGGATCACCT T C TIA1,C2orf42 Ensembl:ENSG00000116001,Ensembl:ENSG00000115998 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1181203444 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6547,RMVar_hsa_circ_343601,RMVar_hsa_circ_299907,RMVar_hsa_circ_300794,RMVar_hsa_circ_201007,RMVar_hsa_circ_201008,RMVar_hsa_circ_201009,RMVar_hsa_circ_201010,RMVar_hsa_circ_360251,RMVar_hsa_circ_361415,RMVar_hsa_circ_48873,RMVar_hsa_circ_288024,RMVar_hsa_circ_305978,RMVar_hsa_circ_65868,RMVar_hsa_circ_37948,RMVar_hsa_circ_201012,RMVar_hsa_circ_201011,RMVar_hsa_circ_291604,RMVar_hsa_circ_55380 45550 RMVar_ID_45550 Human_SNP_ID_76817272 A-to-I Human chr2 - 70234833 70234833 70234833 TTATTTAGCCGGGCACAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGCAG TTATTTAGCCGGGCACAGTGGCTCACACCTGTCATCCCAGCACTTTGGGAGGCCGAGGCAGGCAG T G TIA1,C2orf42 Ensembl:ENSG00000116001,Ensembl:ENSG00000115998 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs940600084 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_299907,RMVar_hsa_circ_201009,RMVar_hsa_circ_361415,RMVar_hsa_circ_305978,RMVar_hsa_circ_201011,RMVar_hsa_circ_55380,RMVar_hsa_circ_292455,RMVar_hsa_circ_201017,RMVar_hsa_circ_201018,RMVar_hsa_circ_336223,RMVar_hsa_circ_201021,RMVar_hsa_circ_340294,RMVar_hsa_circ_201024,RMVar_hsa_circ_302203,RMVar_hsa_circ_201025,RMVar_hsa_circ_316765 45551 RMVar_ID_45551 Human_SNP_ID_76817389 A-to-I Human chr2 - 70235224 70235224 70235224 CTTAGTAGAGATGGGGTTTCTCCATGTTGGTCAGGCTGGTTTAGAACTCCCGACCTCAGGTGATC CTTAGTAGAGATGGGGTTTCTCCATGTTGGTCTGGCTGGTTTAGAACTCCCGACCTCAGGTGATC T A TIA1,C2orf42 Ensembl:ENSG00000116001,Ensembl:ENSG00000115998 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1196742285 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_299907,RMVar_hsa_circ_201009,RMVar_hsa_circ_361415,RMVar_hsa_circ_305978,RMVar_hsa_circ_201011,RMVar_hsa_circ_55380,RMVar_hsa_circ_292455,RMVar_hsa_circ_201017,RMVar_hsa_circ_201018,RMVar_hsa_circ_336223,RMVar_hsa_circ_201021,RMVar_hsa_circ_340294,RMVar_hsa_circ_201024,RMVar_hsa_circ_302203,RMVar_hsa_circ_201025,RMVar_hsa_circ_316765 45552 RMVar_ID_45552 Human_SNP_ID_76817786 A-to-I Human chr2 - 70236364 70236364 70236364 AGAAACCCCGTCTCTACTAAAAATACAAAATTAGCTGGGTGTGGTCACGCATGCCTGTAATCCCA AGAAACCCCGTCTCTACTAAAAATACAAAATTGGCTGGGTGTGGTCACGCATGCCTGTAATCCCA T C TIA1,C2orf42 Ensembl:ENSG00000116001,Ensembl:ENSG00000115998 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1036660920 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_201018,RMVar_hsa_circ_201027 45553 RMVar_ID_45553 Human_SNP_ID_76818043 A-to-I Human chr2 - 70237375 70237375 70237375 CTTTTTTGAGACATAGTCTCACTCTGTTGCCCAGGCTGGAGTGCAGTGGTGCAACCTCAGCTAAC CTTTTTTGAGACATAGTCTCACTCTGTTGCCCGGGCTGGAGTGCAGTGGTGCAACCTCAGCTAAC T C TIA1,C2orf42 Ensembl:ENSG00000116001,Ensembl:ENSG00000115998 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1423328493 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_201018,RMVar_hsa_circ_201027 45554 RMVar_ID_45554 Human_SNP_ID_76818496 A-to-I Human chr2 - 70238794 70238794 70238794 TTTCCACCTTGGCCTCCAAAAGTGCTGGGATTACAGATGTGAGCCACTGCCCCTAATCTAAACCC TTTCCACCTTGGCCTCCAAAAGTGCTGGGATTGCAGATGTGAGCCACTGCCCCTAATCTAAACCC T C TIA1,C2orf42 Ensembl:ENSG00000116001,Ensembl:ENSG00000115998 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs766092988 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569741 RMVar_hsa_circ_201018,RMVar_hsa_circ_201027 45555 RMVar_ID_45555 Human_SNP_ID_76818499 A-to-I Human chr2 - 70238806 70238806 70238806 GCTAAAGTGATCTTTCCACCTTGGCCTCCAAAAGTGCTGGGATTACAGATGTGAGCCACTGCCCC GCTAAAGTGATCTTTCCACCTTGGCCTCCAAATGTGCTGGGATTACAGATGTGAGCCACTGCCCC T A TIA1,C2orf42 Ensembl:ENSG00000116001,Ensembl:ENSG00000115998 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1438136665 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569741 RMVar_hsa_circ_201018,RMVar_hsa_circ_201027 45556 RMVar_ID_45556 Human_SNP_ID_76818500 A-to-I Human chr2 - 70238808 70238808 70238808 TGGCTAAAGTGATCTTTCCACCTTGGCCTCCAAAAGTGCTGGGATTACAGATGTGAGCCACTGCC TGGCTAAAGTGATCTTTCCACCTTGGCCTCCAGAAGTGCTGGGATTACAGATGTGAGCCACTGCC T C TIA1,C2orf42 Ensembl:ENSG00000116001,Ensembl:ENSG00000115998 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs367625304 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569741 RMVar_hsa_circ_201018,RMVar_hsa_circ_201027 45557 RMVar_ID_45557 Human_SNP_ID_76819445 A-to-I Human chr2 - 70242347 70242347 70242347 TTTGTGTTTTTAGTAGAGGCAAGTTTCAACATATTGGCCAGGCTGATCTCGAACTCCTGAGCTCA TTTGTGTTTTTAGTAGAGGCAAGTTTCAACATGTTGGCCAGGCTGATCTCGAACTCCTGAGCTCA T C TIA1,C2orf42 Ensembl:ENSG00000116001,Ensembl:ENSG00000115998 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs560910984 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25561634 RMVar_hsa_circ_201027 45558 RMVar_ID_45558 Human_SNP_ID_76819689 A-to-I Human chr2 - 70243172 70243172 70243172 ATCTTCCCACCTTAGCCTCCCAAAGTGGGATTATAGGTGTGAGCCACCGTGCCTGGTGTTTACAC ATCTTCCCACCTTAGCCTCCCAAAGTGGGATTGTAGGTGTGAGCCACCGTGCCTGGTGTTTACAC T C TIA1,C2orf42 Ensembl:ENSG00000116001,Ensembl:ENSG00000115998 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1402680840 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_201027 45559 RMVar_ID_45559 Human_SNP_ID_76820526 A-to-I Human chr2 - 70246199 70246199 70246199 GTATAATTGGCTGGGCACAGTGGCTCACGCCTATAATCCTAACACTTTGGGGGGCTGAGGAGGGT GTATAATTGGCTGGGCACAGTGGCTCACGCCTTTAATCCTAACACTTTGGGGGGCTGAGGAGGGT T A TIA1,C2orf42 Ensembl:ENSG00000116001,Ensembl:ENSG00000115998 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs933112579 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_201027 45560 RMVar_ID_45560 Human_SNP_ID_76820527 A-to-I Human chr2 - 70246199 70246199 70246199 GTATAATTGGCTGGGCACAGTGGCTCACGCCTATAATCCTAACACTTTGGGGGGCTGAGGAGGGT GTATAATTGGCTGGGCACAGTGGCTCACGCCTGTAATCCTAACACTTTGGGGGGCTGAGGAGGGT T C TIA1,C2orf42 Ensembl:ENSG00000116001,Ensembl:ENSG00000115998 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs933112579 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_201027 45561 RMVar_ID_45561 Human_SNP_ID_76826978 A-to-I Human chr2 + 70267950 70267950 70267950 TCTCTGCCTCAGCCTCCCGAGTAGTTGGGATCACAGGCGCCCACCACCATGCCCGGCTAATTTTT TCTCTGCCTCAGCCTCCCGAGTAGTTGGGATCTCAGGCGCCCACCACCATGCCCGGCTAATTTTT A T PCYOX1 Ensembl:ENSG00000116005 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232303979 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79857,RMVar_hsa_circ_201030,RMVar_hsa_circ_266223,RMVar_hsa_circ_201031,RMVar_hsa_circ_201032 45562 RMVar_ID_45562 Human_SNP_ID_76831543 A-to-I Human chr2 - 70284498 70284498 70284498 ATGCCTCTGGTCCCAGCTACTTGAGAGGCTGAAGTGGGAGGATCACTTGAGCCCAGGAGGTCAAG ATGCCTCTGGTCCCAGCTACTTGAGAGGCTGAGGTGGGAGGATCACTTGAGCCCAGGAGGTCAAG T C SNRPG Ensembl:ENSG00000143977 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1049012800 Functional Loss SNV dbSNP153 33..33 33 - - - 45563 RMVar_ID_45563 Human_SNP_ID_76831760 A-to-I Human chr2 - 70285389 70285389 70285389 TTTTGTATTTTTAGTAGAGACAGGGTTTCACTATGTTGGCCAGGCTGGTCTCAAACTCCTGACCG TTTTGTATTTTTAGTAGAGACAGGGTTTCACTGTGTTGGCCAGGCTGGTCTCAAACTCCTGACCG T C SNRPG Ensembl:ENSG00000143977 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs372306840 Functional Loss SNV dbSNP153 33..33 33 - - - 45564 RMVar_ID_45564 Human_SNP_ID_76831807 A-to-I Human chr2 - 70285533 70285533 70285533 GAGTCTCACTGTGTCACCGAGGCTGGAGTGCAATGGTGTGGTCTCGGGTCACTGCAACCTCCGCC GAGTCTCACTGTGTCACCGAGGCTGGAGTGCAGTGGTGTGGTCTCGGGTCACTGCAACCTCCGCC T C SNRPG Ensembl:ENSG00000143977 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs375860107 Functional Loss SNV dbSNP153 33..33 33 - - - 45565 RMVar_ID_45565 Human_SNP_ID_76831950 A-to-I Human chr2 - 70286018 70286018 70286018 GGAGGCTGAGGCAGGAAGTCAAAGCTGCAGTGAGCTGAGATCACACTACTGCACTCCAATCTTTG GGAGGCTGAGGCAGGAAGTCAAAGCTGCAGTGGGCTGAGATCACACTACTGCACTCCAATCTTTG T C SNRPG Ensembl:ENSG00000143977 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1253889466 Functional Loss SNV dbSNP153 33..33 33 - - - 45566 RMVar_ID_45566 Human_SNP_ID_76833026 A-to-I Human chr2 - 70290064 70290064 70290064 GCTGAGGGGGAGTATATTTTTCGAGGCCAGGAATTCAGGACCAGCCTGGGCAACATAATGAGACT GCTGAGGGGGAGTATATTTTTCGAGGCCAGGAGTTCAGGACCAGCCTGGGCAACATAATGAGACT T C SNRPG Ensembl:ENSG00000143977 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1323679640 Functional Loss SNV dbSNP153 33..33 33 - - - 45567 RMVar_ID_45567 Human_SNP_ID_76922437 A-to-I Human chr2 - 70659119 70659119 70659119 TTTTTTAGACGGAGCTTTGCTCTTTGTTGCCCAGGCTGGAGTGCAGTGGTGCAATCTTAGCTCAC TTTTTTAGACGGAGCTTTGCTCTTTGTTGCCCGGGCTGGAGTGCAGTGGTGCAATCTTAGCTCAC T C ADD2 Ensembl:ENSG00000075340 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1417458049 Functional Loss SNV dbSNP153 33..33 33 - - - 45568 RMVar_ID_45568 Human_SNP_ID_76958707 A-to-I Human chr2 + 70810966 70810966 70810966 TATTCATCAAATATCTGCCAATGATGAAAATAAACATGTGAAAATATTCTGTAAATTCTACGGCA TATTCATCAAATATCTGCCAATGATGAAAATACACATGTGAAAATATTCTGTAAATTCTACGGCA A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1558609344 Functional Loss SNV dbSNP153 33..33 33 - - - 45569 RMVar_ID_45569 Human_SNP_ID_76958816 A-to-I Human chr2 - 70811440 70811440 70811440 GGTCATGGCAGAGGGGATGGCAGTGCTGAGGCAGAACAGGCAGGGCACCAAGGCACAGGATATCT GGTCATGGCAGAGGGGATGGCAGTGCTGAGGCGGAACAGGCAGGGCACCAAGGCACAGGATATCT T C CLEC4F,AC007395.1 Ensembl:ENSG00000152672,Ensembl:ENSG00000231386 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs782532623 Functional Loss SNV dbSNP153 33..33 33 - - - 45570 RMVar_ID_45570 Human_SNP_ID_77004662 A-to-I Human chr2 - 70987472 70987470 70987472 AACAGTACATATTGGAATGAAGTCCCTATGAGAGCCATTTCTGGCCATGTTCTATACCTCAAAGT AACAGTACATATTGGAATGAAGTCCCTATGAG__CCATTTCTGGCCATGTTCTATACCTCAAAGT GCT G AC007040.2,TEX261 Ensembl:ENSG00000258881,Ensembl:ENSG00000144043 Protein coding,Protein coding intron,3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1441636773 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_1922536,Human_RBP_ID_8524309,Human_RBP_ID_13951487,Human_RBP_ID_17276743,Human_RBP_ID_23882738,Human_RBP_ID_26487215 Human_miRNA_ID_258103,Human_miRNA_ID_261897,Human_miRNA_ID_1658470 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 45571 RMVar_ID_45571 Human_SNP_ID_77046827 A-to-I Human chr2 + 71141848 71141848 71141848 GGTCAGGAGTTTTAGACCTGCCTGGCCAACATAGTGAAACCCCATCTCTACTAAAAATACGAAAA GGTCAGGAGTTTTAGACCTGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACGAAAA A G MPHOSPH10 Ensembl:ENSG00000124383 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1178066613 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17683,RMVar_hsa_circ_329629,RMVar_hsa_circ_93531,RMVar_hsa_circ_201060,RMVar_hsa_circ_201061 45572 RMVar_ID_45572 Human_SNP_ID_77047157 A-to-I Human chr2 + 71143313 71143313 71143313 TGCCACCAAGCCCGTCTAATTTTTTGTATTTTAGTAGAGACAGGGTTTCATTATGTTAGCCAGGA TGCCACCAAGCCCGTCTAATTTTTTGTATTTTGGTAGAGACAGGGTTTCATTATGTTAGCCAGGA A G MPHOSPH10 Ensembl:ENSG00000124383 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1419920998 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17683,RMVar_hsa_circ_329629,RMVar_hsa_circ_93531,RMVar_hsa_circ_201060,RMVar_hsa_circ_201061 45573 RMVar_ID_45573 Human_SNP_ID_77094864 A-to-I Human chr2 + 71337578 71337578 71337578 CAGGCGCGCACCACCATGCCTGGCTACGTTTTATATTTTTTGTAGAGATGGGATTTTGCCATGTT CAGGCGCGCACCACCATGCCTGGCTACGTTTTGTATTTTTTGTAGAGATGGGATTTTGCCATGTT A G ZNF638 Ensembl:ENSG00000075292 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs906115721 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13952963 RMVar_hsa_circ_88409,RMVar_hsa_circ_201064,RMVar_hsa_circ_201063 45574 RMVar_ID_45574 Human_SNP_ID_77095313 A-to-I Human chr2 + 71339221 71339221 71339221 GCACCCAGGCTGGAGTGCAGTGGCACCATCTCAGTGCACTGCAGCCTCCACCTCCCAGGTGCAAG GCACCCAGGCTGGAGTGCAGTGGCACCATCTCCGTGCACTGCAGCCTCCACCTCCCAGGTGCAAG A C ZNF638 Ensembl:ENSG00000075292 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965403016 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2661125,Human_RBP_ID_9110299 RMVar_hsa_circ_88409,RMVar_hsa_circ_201064,RMVar_hsa_circ_201063 45575 RMVar_ID_45575 Human_SNP_ID_77099596 A-to-I Human chr2 + 71354485 71354485 71354485 GGCTGGGCATGGTGGCTCACGCCTGTAATCCTAACACTTTTGGGAGGCCGAGGCAGGTGGATCAC GGCTGGGCATGGTGGCTCACGCCTGTAATCCTCACACTTTTGGGAGGCCGAGGCAGGTGGATCAC A C ZNF638 Ensembl:ENSG00000075292 Protein coding intron GSE107867 ASD brains,cerebellum;ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1401748952 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25562584 RMVar_hsa_circ_6755,RMVar_hsa_circ_88409,RMVar_hsa_circ_201063,RMVar_hsa_circ_345658,RMVar_hsa_circ_34103,RMVar_hsa_circ_32719,RMVar_hsa_circ_324133,RMVar_hsa_circ_328047,RMVar_hsa_circ_327584,RMVar_hsa_circ_281586,RMVar_hsa_circ_54993,RMVar_hsa_circ_73000,RMVar_hsa_circ_44254,RMVar_hsa_circ_4682,RMVar_hsa_circ_201067 45576 RMVar_ID_45576 Human_SNP_ID_77099760 A-to-I Human chr2 + 71355032 71355032 71355032 GCTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCAATCTCGGCTCACTGCAAGCTCCGCCTCCCGGG GCTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCCATCTCGGCTCACTGCAAGCTCCGCCTCCCGGG A C ZNF638 Ensembl:ENSG00000075292 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs965770318 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6755,RMVar_hsa_circ_88409,RMVar_hsa_circ_201063,RMVar_hsa_circ_345658,RMVar_hsa_circ_34103,RMVar_hsa_circ_32719,RMVar_hsa_circ_324133,RMVar_hsa_circ_328047,RMVar_hsa_circ_327584,RMVar_hsa_circ_281586,RMVar_hsa_circ_54993,RMVar_hsa_circ_73000,RMVar_hsa_circ_44254,RMVar_hsa_circ_4682,RMVar_hsa_circ_201067 45577 RMVar_ID_45577 Human_SNP_ID_77099761 A-to-I Human chr2 + 71355032 71355032 71355032 GCTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCAATCTCGGCTCACTGCAAGCTCCGCCTCCCGGG GCTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCGATCTCGGCTCACTGCAAGCTCCGCCTCCCGGG A G ZNF638 Ensembl:ENSG00000075292 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs965770318 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6755,RMVar_hsa_circ_88409,RMVar_hsa_circ_201063,RMVar_hsa_circ_345658,RMVar_hsa_circ_34103,RMVar_hsa_circ_32719,RMVar_hsa_circ_324133,RMVar_hsa_circ_328047,RMVar_hsa_circ_327584,RMVar_hsa_circ_281586,RMVar_hsa_circ_54993,RMVar_hsa_circ_73000,RMVar_hsa_circ_44254,RMVar_hsa_circ_4682,RMVar_hsa_circ_201067 45578 RMVar_ID_45578 Human_SNP_ID_77099800 A-to-I Human chr2 + 71355144 71355136 71355144 GTGCCCGCCACAACGCCTGGCTAATTTTTTGTATTTTTAGTAGAGACAGGGTTTCACAGTAGTGT GTGCCCGCCACAACGCCTGGCTAAT________TTTTTAGTAGAGACAGGGTTTCACAGTAGTGT TTTTTTGTA T ZNF638 Ensembl:ENSG00000075292 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1342645062 Functional Loss DEL dbSNP153 26..33 33 - - - RMVar_hsa_circ_6755,RMVar_hsa_circ_88409,RMVar_hsa_circ_201063,RMVar_hsa_circ_345658,RMVar_hsa_circ_34103,RMVar_hsa_circ_32719,RMVar_hsa_circ_324133,RMVar_hsa_circ_328047,RMVar_hsa_circ_327584,RMVar_hsa_circ_281586,RMVar_hsa_circ_54993,RMVar_hsa_circ_73000,RMVar_hsa_circ_44254,RMVar_hsa_circ_4682,RMVar_hsa_circ_201067 45579 RMVar_ID_45579 Human_SNP_ID_77100188 A-to-I Human chr2 + 71356534 71356534 71356534 AAGTTGCAGATTAGTTGCTGGCTCATGACTGTAATCTGAGCACTTTGGAAGGCTGAGACAGGTAG AAGTTGCAGATTAGTTGCTGGCTCATGACTGTGATCTGAGCACTTTGGAAGGCTGAGACAGGTAG A G ZNF638 Ensembl:ENSG00000075292 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1055674 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13953683 RMVar_hsa_circ_6755,RMVar_hsa_circ_88409,RMVar_hsa_circ_201063,RMVar_hsa_circ_345658,RMVar_hsa_circ_201071,RMVar_hsa_circ_32719,RMVar_hsa_circ_324133,RMVar_hsa_circ_328047,RMVar_hsa_circ_327584,RMVar_hsa_circ_54993,RMVar_hsa_circ_73000,RMVar_hsa_circ_44254,RMVar_hsa_circ_284278,RMVar_hsa_circ_338612,RMVar_hsa_circ_4682,RMVar_hsa_circ_201067,RMVar_hsa_circ_353857,RMVar_hsa_circ_361750,RMVar_hsa_circ_323094,RMVar_hsa_circ_338274,RMVar_hsa_circ_295867,RMVar_hsa_circ_69432,RMVar_hsa_circ_275508,RMVar_hsa_circ_201072,RMVar_hsa_circ_201069,RMVar_hsa_circ_201070,RMVar_hsa_circ_201068 45580 RMVar_ID_45580 Human_SNP_ID_77102828 A-to-I Human chr2 + 71365819 71365819 71365819 ATGGCTCACTGCAGCCTCGATCTCCTGGGCTCAAGTGATCCTCCTGCCTCATCTTCCCAAGTAGC ATGGCTCACTGCAGCCTCGATCTCCTGGGCTCGAGTGATCCTCCTGCCTCATCTTCCCAAGTAGC A G ZNF638 Ensembl:ENSG00000075292 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,cerebellum - 29129909,30559470 RNA-Seq:(High) rs1052661174 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8524499 RMVar_hsa_circ_6755,RMVar_hsa_circ_88409,RMVar_hsa_circ_201063,RMVar_hsa_circ_345658,RMVar_hsa_circ_31128,RMVar_hsa_circ_201071,RMVar_hsa_circ_32719,RMVar_hsa_circ_324133,RMVar_hsa_circ_327584,RMVar_hsa_circ_54993,RMVar_hsa_circ_73000,RMVar_hsa_circ_44254,RMVar_hsa_circ_284278,RMVar_hsa_circ_338612,RMVar_hsa_circ_4682,RMVar_hsa_circ_201067,RMVar_hsa_circ_353857,RMVar_hsa_circ_361750,RMVar_hsa_circ_323094,RMVar_hsa_circ_295867,RMVar_hsa_circ_69432,RMVar_hsa_circ_275508,RMVar_hsa_circ_201072,RMVar_hsa_circ_3533,RMVar_hsa_circ_201069,RMVar_hsa_circ_201070,RMVar_hsa_circ_201068,RMVar_hsa_circ_300440,RMVar_hsa_circ_345801,RMVar_hsa_circ_268182,RMVar_hsa_circ_45527,RMVar_hsa_circ_60785,RMVar_hsa_circ_201074,RMVar_hsa_circ_201075,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_334397,RMVar_hsa_circ_354362,RMVar_hsa_circ_362011,RMVar_hsa_circ_352639,RMVar_hsa_circ_343412,RMVar_hsa_circ_350918,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_55720,RMVar_hsa_circ_201077,RMVar_hsa_circ_201079,RMVar_hsa_circ_201080,RMVar_hsa_circ_201078 45581 RMVar_ID_45581 Human_SNP_ID_77102856 A-to-I Human chr2 + 71365947 71365947 71365947 TGCCATGTTGCTCAGGCTGGTCTCGAACTACTAGGTTCAGGCAGTCCTTCCACGTCAGCTTCCCT TGCCATGTTGCTCAGGCTGGTCTCGAACTACTGGGTTCAGGCAGTCCTTCCACGTCAGCTTCCCT A G ZNF638 Ensembl:ENSG00000075292 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1288949795 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6755,RMVar_hsa_circ_88409,RMVar_hsa_circ_201063,RMVar_hsa_circ_345658,RMVar_hsa_circ_31128,RMVar_hsa_circ_201071,RMVar_hsa_circ_32719,RMVar_hsa_circ_324133,RMVar_hsa_circ_327584,RMVar_hsa_circ_54993,RMVar_hsa_circ_73000,RMVar_hsa_circ_44254,RMVar_hsa_circ_284278,RMVar_hsa_circ_338612,RMVar_hsa_circ_4682,RMVar_hsa_circ_201067,RMVar_hsa_circ_353857,RMVar_hsa_circ_361750,RMVar_hsa_circ_323094,RMVar_hsa_circ_295867,RMVar_hsa_circ_69432,RMVar_hsa_circ_275508,RMVar_hsa_circ_201072,RMVar_hsa_circ_3533,RMVar_hsa_circ_201069,RMVar_hsa_circ_201070,RMVar_hsa_circ_201068,RMVar_hsa_circ_300440,RMVar_hsa_circ_345801,RMVar_hsa_circ_268182,RMVar_hsa_circ_45527,RMVar_hsa_circ_60785,RMVar_hsa_circ_201074,RMVar_hsa_circ_201075,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_334397,RMVar_hsa_circ_354362,RMVar_hsa_circ_362011,RMVar_hsa_circ_352639,RMVar_hsa_circ_343412,RMVar_hsa_circ_350918,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_55720,RMVar_hsa_circ_201077,RMVar_hsa_circ_201079,RMVar_hsa_circ_201080,RMVar_hsa_circ_201078 45582 RMVar_ID_45582 Human_SNP_ID_77105484 A-to-I Human chr2 + 71374878 71374878 71374878 CACACGATGGAGAGGTAGCACTGAGCTGAGATAGCACCATGGCACCCCAGCCTGGGCAACAGAGC CACACGATGGAGAGGTAGCACTGAGCTGAGATGGCACCATGGCACCCCAGCCTGGGCAACAGAGC A G AC007878.1,ZNF638 Ensembl:ENSG00000281195,Ensembl:ENSG00000075292 lincRNA,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992915068 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6946094,Human_RBP_ID_13954517,Human_RBP_ID_21932201,Human_RBP_ID_23883141 Human_Splice_Rec_260212 Human_miRNA_ID_3189954 RMVar_hsa_circ_6755,RMVar_hsa_circ_88409,RMVar_hsa_circ_201063,RMVar_hsa_circ_5314,RMVar_hsa_circ_31128,RMVar_hsa_circ_32719,RMVar_hsa_circ_327584,RMVar_hsa_circ_54993,RMVar_hsa_circ_44254,RMVar_hsa_circ_284278,RMVar_hsa_circ_338612,RMVar_hsa_circ_4682,RMVar_hsa_circ_353857,RMVar_hsa_circ_361750,RMVar_hsa_circ_295867,RMVar_hsa_circ_69432,RMVar_hsa_circ_3533,RMVar_hsa_circ_201069,RMVar_hsa_circ_201070,RMVar_hsa_circ_201068,RMVar_hsa_circ_268182,RMVar_hsa_circ_45527,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_334397,RMVar_hsa_circ_354362,RMVar_hsa_circ_362011,RMVar_hsa_circ_352639,RMVar_hsa_circ_343412,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_201077,RMVar_hsa_circ_201079,RMVar_hsa_circ_201080,RMVar_hsa_circ_201078,RMVar_hsa_circ_345650,RMVar_hsa_circ_44659,RMVar_hsa_circ_52069,RMVar_hsa_circ_25874,RMVar_hsa_circ_201081,RMVar_hsa_circ_201083,RMVar_hsa_circ_201082 45583 RMVar_ID_45583 Human_SNP_ID_77105485 A-to-I Human chr2 + 71374878 71374878 71374878 CACACGATGGAGAGGTAGCACTGAGCTGAGATAGCACCATGGCACCCCAGCCTGGGCAACAGAGC CACACGATGGAGAGGTAGCACTGAGCTGAGATTGCACCATGGCACCCCAGCCTGGGCAACAGAGC A T AC007878.1,ZNF638 Ensembl:ENSG00000281195,Ensembl:ENSG00000075292 lincRNA,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992915068 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6946094,Human_RBP_ID_13954517,Human_RBP_ID_21932201,Human_RBP_ID_23883141 Human_Splice_Rec_260212 Human_miRNA_ID_3189954 RMVar_hsa_circ_6755,RMVar_hsa_circ_88409,RMVar_hsa_circ_201063,RMVar_hsa_circ_5314,RMVar_hsa_circ_31128,RMVar_hsa_circ_32719,RMVar_hsa_circ_327584,RMVar_hsa_circ_54993,RMVar_hsa_circ_44254,RMVar_hsa_circ_284278,RMVar_hsa_circ_338612,RMVar_hsa_circ_4682,RMVar_hsa_circ_353857,RMVar_hsa_circ_361750,RMVar_hsa_circ_295867,RMVar_hsa_circ_69432,RMVar_hsa_circ_3533,RMVar_hsa_circ_201069,RMVar_hsa_circ_201070,RMVar_hsa_circ_201068,RMVar_hsa_circ_268182,RMVar_hsa_circ_45527,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_334397,RMVar_hsa_circ_354362,RMVar_hsa_circ_362011,RMVar_hsa_circ_352639,RMVar_hsa_circ_343412,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_201077,RMVar_hsa_circ_201079,RMVar_hsa_circ_201080,RMVar_hsa_circ_201078,RMVar_hsa_circ_345650,RMVar_hsa_circ_44659,RMVar_hsa_circ_52069,RMVar_hsa_circ_25874,RMVar_hsa_circ_201081,RMVar_hsa_circ_201083,RMVar_hsa_circ_201082 45584 RMVar_ID_45584 Human_SNP_ID_77106832 A-to-I Human chr2 + 71379833 71379833 71379833 GGCCATGCTAATTACCGTATCATTCCAATTTTAGTATATGTGCTGCTGAAGGGAGCGTTTTTCTA GGCCATGCTAATTACCGTATCATTCCAATTTTGGTATATGTGCTGCTGAAGGGAGCGTTTTTCTA A G ZNF638 Ensembl:ENSG00000075292 Protein coding intron GSE107867 ASD brains,cerebellum;ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1319974079 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6946230,Human_RBP_ID_13954809,Human_RBP_ID_17208032 RMVar_hsa_circ_6755,RMVar_hsa_circ_88409,RMVar_hsa_circ_201063,RMVar_hsa_circ_5314,RMVar_hsa_circ_31128,RMVar_hsa_circ_32719,RMVar_hsa_circ_327584,RMVar_hsa_circ_54993,RMVar_hsa_circ_44254,RMVar_hsa_circ_284278,RMVar_hsa_circ_338612,RMVar_hsa_circ_4682,RMVar_hsa_circ_353857,RMVar_hsa_circ_361750,RMVar_hsa_circ_295867,RMVar_hsa_circ_69432,RMVar_hsa_circ_3533,RMVar_hsa_circ_201069,RMVar_hsa_circ_201070,RMVar_hsa_circ_201068,RMVar_hsa_circ_268182,RMVar_hsa_circ_45527,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_334397,RMVar_hsa_circ_354362,RMVar_hsa_circ_362011,RMVar_hsa_circ_352639,RMVar_hsa_circ_343412,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_201077,RMVar_hsa_circ_201079,RMVar_hsa_circ_201080,RMVar_hsa_circ_201078,RMVar_hsa_circ_345650,RMVar_hsa_circ_44659,RMVar_hsa_circ_52069,RMVar_hsa_circ_25874,RMVar_hsa_circ_201081,RMVar_hsa_circ_201083,RMVar_hsa_circ_201082 45585 RMVar_ID_45585 Human_SNP_ID_77108570 A-to-I Human chr2 + 71386219 71386219 71386219 GCAAGGCTGATCTGGGAGGATTGCTTGAGCCCAGGAGGTCGACGCTTCAGTGAACTGTGATCGTG GCAAGGCTGATCTGGGAGGATTGCTTGAGCCCGGGAGGTCGACGCTTCAGTGAACTGTGATCGTG A G ZNF638 Ensembl:ENSG00000075292 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1134109 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1589848,Human_RBP_ID_6946339,Human_RBP_ID_13955088 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 45586 RMVar_ID_45586 Human_SNP_ID_77109001 A-to-I Human chr2 + 71387591 71387591 71387591 TACTCAGGAGGCTGAGGCAGGAGAATTGCCTGAACCTGGGAGGTGGAGGTTGTAATGAGCTGAGA TACTCAGGAGGCTGAGGCAGGAGAATTGCCTGGACCTGGGAGGTGGAGGTTGTAATGAGCTGAGA A G ZNF638 Ensembl:ENSG00000075292 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs544556889 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13955142 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_201088,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 45587 RMVar_ID_45587 Human_SNP_ID_77122231 A-to-I Human chr2 + 71432304 71432304 71432304 CTAACTGCAACCCTTTCCTCCCAGGCTCAAGCAATCCTCTCACCTCAGCCTCATGAGTAGCTGGG CTAACTGCAACCCTTTCCTCCCAGGCTCAAGCGATCCTCTCACCTCAGCCTCATGAGTAGCTGGG A G ZNF638 Ensembl:ENSG00000075292 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1173620701 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3533,RMVar_hsa_circ_40482,RMVar_hsa_circ_11732,RMVar_hsa_circ_201092,RMVar_hsa_circ_201100,RMVar_hsa_circ_299668,RMVar_hsa_circ_353766,RMVar_hsa_circ_201102,RMVar_hsa_circ_66063,RMVar_hsa_circ_358799 45588 RMVar_ID_45588 Human_SNP_ID_77328163 A-to-I Human chr2 - 72232816 72232816 72232816 CCACCCGCCTCAGCCTGCCAAAGGCTAGGATTATAGGCATGAGCCACTGCGCCTGGCCCGGGTTT CCACCCGCCTCAGCCTGCCAAAGGCTAGGATTGTAGGCATGAGCCACTGCGCCTGGCCCGGGTTT T C EXOC6B Ensembl:ENSG00000144036 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1366129904 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101273,RMVar_hsa_circ_108496,RMVar_hsa_circ_127475,RMVar_hsa_circ_127360,RMVar_hsa_circ_201122,RMVar_hsa_circ_84883,RMVar_hsa_circ_89363,RMVar_hsa_circ_201124,RMVar_hsa_circ_201125,RMVar_hsa_circ_201123,RMVar_hsa_circ_125703,RMVar_hsa_circ_201121,RMVar_hsa_circ_101965,RMVar_hsa_circ_201128,RMVar_hsa_circ_85103,RMVar_hsa_circ_94265,RMVar_hsa_circ_201130,RMVar_hsa_circ_83695,RMVar_hsa_circ_201131,RMVar_hsa_circ_201129,RMVar_hsa_circ_201126,RMVar_hsa_circ_201127 45589 RMVar_ID_45589 Human_SNP_ID_77343991 A-to-I Human chr2 - 72305698 72305698 72305698 TACATTAGAGTGAAACTTTATATAACTATTTAATCATTACAAGTCCATGAGGTAGCTATTATTAT TACATTAGAGTGAAACTTTATATAACTATTTAGTCATTACAAGTCCATGAGGTAGCTATTATTAT T C EXOC6B Ensembl:ENSG00000144036 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042806288 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101273,RMVar_hsa_circ_108496,RMVar_hsa_circ_127475,RMVar_hsa_circ_127360,RMVar_hsa_circ_201122,RMVar_hsa_circ_84883,RMVar_hsa_circ_89363,RMVar_hsa_circ_201124,RMVar_hsa_circ_201125,RMVar_hsa_circ_201123,RMVar_hsa_circ_125703,RMVar_hsa_circ_201121,RMVar_hsa_circ_101965,RMVar_hsa_circ_201128,RMVar_hsa_circ_85103,RMVar_hsa_circ_94265,RMVar_hsa_circ_201130,RMVar_hsa_circ_83695,RMVar_hsa_circ_201131,RMVar_hsa_circ_201129,RMVar_hsa_circ_201126,RMVar_hsa_circ_201127 45590 RMVar_ID_45590 Human_SNP_ID_77379515 A-to-I Human chr2 - 72462667 72462667 72462667 GTTTCTCACAGTTCTGGAGGCTGCAAAGTCCAATATTAAGATGTCAGCAGATTCAGTGTCTGATA GTTTCTCACAGTTCTGGAGGCTGCAAAGTCCAGTATTAAGATGTCAGCAGATTCAGTGTCTGATA T C EXOC6B Ensembl:ENSG00000144036 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1158569268 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569751 RMVar_hsa_circ_51412,RMVar_hsa_circ_101273,RMVar_hsa_circ_108496,RMVar_hsa_circ_127475,RMVar_hsa_circ_201122,RMVar_hsa_circ_84883,RMVar_hsa_circ_89363,RMVar_hsa_circ_201124,RMVar_hsa_circ_201125,RMVar_hsa_circ_201123,RMVar_hsa_circ_125703,RMVar_hsa_circ_101965,RMVar_hsa_circ_40617,RMVar_hsa_circ_201128,RMVar_hsa_circ_85103,RMVar_hsa_circ_201130,RMVar_hsa_circ_83695,RMVar_hsa_circ_201129,RMVar_hsa_circ_201126,RMVar_hsa_circ_201127,RMVar_hsa_circ_293421,RMVar_hsa_circ_318810,RMVar_hsa_circ_339303,RMVar_hsa_circ_21183,RMVar_hsa_circ_40616,RMVar_hsa_circ_18810,RMVar_hsa_circ_104195,RMVar_hsa_circ_347551,RMVar_hsa_circ_201135 45591 RMVar_ID_45591 Human_SNP_ID_77379531 A-to-I Human chr2 - 72462739 72462739 72462739 GCATGTCTTAGTCCATTCCTGCTCCCATAACAAGATACTGTAGACTGAGAAATTTATAAACAACA GCATGTCTTAGTCCATTCCTGCTCCCATAACAGGATACTGTAGACTGAGAAATTTATAAACAACA T C EXOC6B Ensembl:ENSG00000144036 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1558691855 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51412,RMVar_hsa_circ_101273,RMVar_hsa_circ_108496,RMVar_hsa_circ_127475,RMVar_hsa_circ_201122,RMVar_hsa_circ_84883,RMVar_hsa_circ_89363,RMVar_hsa_circ_201124,RMVar_hsa_circ_201125,RMVar_hsa_circ_201123,RMVar_hsa_circ_125703,RMVar_hsa_circ_101965,RMVar_hsa_circ_40617,RMVar_hsa_circ_201128,RMVar_hsa_circ_85103,RMVar_hsa_circ_201130,RMVar_hsa_circ_83695,RMVar_hsa_circ_201129,RMVar_hsa_circ_201126,RMVar_hsa_circ_201127,RMVar_hsa_circ_293421,RMVar_hsa_circ_318810,RMVar_hsa_circ_339303,RMVar_hsa_circ_21183,RMVar_hsa_circ_40616,RMVar_hsa_circ_18810,RMVar_hsa_circ_104195,RMVar_hsa_circ_347551,RMVar_hsa_circ_201135 45592 RMVar_ID_45592 Human_SNP_ID_77379755 A-to-I Human chr2 - 72463825 72463825 72463825 CCTCCAGAACTGTGAGAATTCTTTTGTTTATAAGCTACCAGTCTATGGGATTTTGTTACATTATT CCTCCAGAACTGTGAGAATTCTTTTGTTTATATGCTACCAGTCTATGGGATTTTGTTACATTATT T A EXOC6B Ensembl:ENSG00000144036 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs927288012 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26668472 RMVar_hsa_circ_51412,RMVar_hsa_circ_101273,RMVar_hsa_circ_108496,RMVar_hsa_circ_127475,RMVar_hsa_circ_201122,RMVar_hsa_circ_84883,RMVar_hsa_circ_89363,RMVar_hsa_circ_201124,RMVar_hsa_circ_201125,RMVar_hsa_circ_201123,RMVar_hsa_circ_125703,RMVar_hsa_circ_101965,RMVar_hsa_circ_40617,RMVar_hsa_circ_201128,RMVar_hsa_circ_85103,RMVar_hsa_circ_201130,RMVar_hsa_circ_83695,RMVar_hsa_circ_201129,RMVar_hsa_circ_201126,RMVar_hsa_circ_201127,RMVar_hsa_circ_293421,RMVar_hsa_circ_318810,RMVar_hsa_circ_339303,RMVar_hsa_circ_21183,RMVar_hsa_circ_40616,RMVar_hsa_circ_18810,RMVar_hsa_circ_104195,RMVar_hsa_circ_347551,RMVar_hsa_circ_201135 45593 RMVar_ID_45593 Human_SNP_ID_77429433 A-to-I Human chr2 - 72678477 72678477 72678477 GCCTCCAACTCCTGGCCTCAAGTGATCCGCTCACCTTGGCTTCCTAAAGTGTTGGGATTGTAAAC GCCTCCAACTCCTGGCCTCAAGTGATCCGCTCTCCTTGGCTTCCTAAAGTGTTGGGATTGTAAAC T A EXOC6B Ensembl:ENSG00000144036 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215580096 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127475,RMVar_hsa_circ_201125,RMVar_hsa_circ_21183,RMVar_hsa_circ_40616,RMVar_hsa_circ_28549,RMVar_hsa_circ_16352,RMVar_hsa_circ_370398,RMVar_hsa_circ_43418,RMVar_hsa_circ_62921,RMVar_hsa_circ_201136,RMVar_hsa_circ_71748,RMVar_hsa_circ_48135,RMVar_hsa_circ_41880,RMVar_hsa_circ_117570,RMVar_hsa_circ_356870,RMVar_hsa_circ_201153,RMVar_hsa_circ_327966,RMVar_hsa_circ_81764,RMVar_hsa_circ_201157,RMVar_hsa_circ_315773,RMVar_hsa_circ_80506,RMVar_hsa_circ_201158,RMVar_hsa_circ_340840,RMVar_hsa_circ_289922,RMVar_hsa_circ_28901,RMVar_hsa_circ_310955,RMVar_hsa_circ_315619 45594 RMVar_ID_45594 Human_SNP_ID_77432527 A-to-I Human chr2 - 72692519 72692518 72692519 GTGAAACCCCGTCTCTTCTAAAAATACAAAAAATTAGCCGGGCATGGTGGTGGGCGCCTGTAGTC GTGAAACCCCGTCTCTTCTAAAAATACAAAAA_TTAGCCGGGCATGGTGGTGGGCGCCTGTAGTC AT A EXOC6B Ensembl:ENSG00000144036 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1314330330 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_127475,RMVar_hsa_circ_201125,RMVar_hsa_circ_21183,RMVar_hsa_circ_40616,RMVar_hsa_circ_28549,RMVar_hsa_circ_16352,RMVar_hsa_circ_370398,RMVar_hsa_circ_43418,RMVar_hsa_circ_62921,RMVar_hsa_circ_201136,RMVar_hsa_circ_71748,RMVar_hsa_circ_48135,RMVar_hsa_circ_41880,RMVar_hsa_circ_117570,RMVar_hsa_circ_356870,RMVar_hsa_circ_201153,RMVar_hsa_circ_327966,RMVar_hsa_circ_81764,RMVar_hsa_circ_201157,RMVar_hsa_circ_315773,RMVar_hsa_circ_80506,RMVar_hsa_circ_201158,RMVar_hsa_circ_340840,RMVar_hsa_circ_289922,RMVar_hsa_circ_28901,RMVar_hsa_circ_310955,RMVar_hsa_circ_315619 45595 RMVar_ID_45595 Human_SNP_ID_77447962 A-to-I Human chr2 - 72763596 72763596 72763596 AACATGGTGAAAACCCATCTCTACCAAAAAATACAAAAATTACCCGGGTGTGGTGGCACGCACCT AACATGGTGAAAACCCATCTCTACCAAAAAATGCAAAAATTACCCGGGTGTGGTGGCACGCACCT T C EXOC6B Ensembl:ENSG00000144036 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1345061428 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116271,RMVar_hsa_circ_201170,RMVar_hsa_circ_201171,RMVar_hsa_circ_85215,RMVar_hsa_circ_201173 45596 RMVar_ID_45596 Human_SNP_ID_77506906 A-to-I Human chr2 - 73015571 73015571 73015571 TCATGCCTCTTATCCCAGCACTTTGAGAGGCCAAGGCAGGGGAATCGCTTGAGCCCAGGAGTTTG TCATGCCTCTTATCCCAGCACTTTGAGAGGCCGAGGCAGGGGAATCGCTTGAGCCCAGGAGTTTG T C SFXN5 Ensembl:ENSG00000144040 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs560960156 Functional Loss SNV dbSNP153 33..33 33 - - - 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_357697,RMVar_hsa_circ_115265,RMVar_hsa_circ_201189,RMVar_hsa_circ_201190,RMVar_hsa_circ_57708,RMVar_hsa_circ_280041,RMVar_hsa_circ_304412,RMVar_hsa_circ_33590,RMVar_hsa_circ_201191 45597 RMVar_ID_45597 Human_SNP_ID_77568450 A-to-I Human chr2 - 73261255 73261255 73261255 CAGGAGTTTGAGACCAGCCTGGCCAACATGGTAAAATCCTGTCTCTACTAAAAGTACAAAAAAAT CAGGAGTTTGAGACCAGCCTGGCCAACATGGTGAAATCCTGTCTCTACTAAAAGTACAAAAAAAT T C FBXO41 Ensembl:ENSG00000163013 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs917558608 Functional Loss SNV dbSNP153 33..33 33 - - - 45598 RMVar_ID_45598 Human_SNP_ID_77573882 A-to-I Human chr2 - 73282595 73282595 73282595 GGGCCCAAGCAATCCTCCCACCTCAGTCTCCCAAGCAGCTGGGACCACAGGCATATGCCACCACA GGGCCCAAGCAATCCTCCCACCTCAGTCTCCCGAGCAGCTGGGACCACAGGCATATGCCACCACA T C FBXO41 Ensembl:ENSG00000163013 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs899053601 Functional Loss SNV dbSNP153 33..33 33 - - - 45599 RMVar_ID_45599 Human_SNP_ID_77617317 A-to-I Human chr2 + 73457922 73457922 73457922 GGGTGTCATGGTGCATGCCTGTAATCCTAGCTACTCGGGAAGCTGAGGCAGGAGAATTGCTTGAA GGGTGTCATGGTGCATGCCTGTAATCCTAGCTCCTCGGGAAGCTGAGGCAGGAGAATTGCTTGAA A C ALMS1-IT1,ALMS1 Ensembl:ENSG00000230002,Ensembl:ENSG00000116127 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459205557 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2627,RMVar_hsa_circ_56813,RMVar_hsa_circ_363390,RMVar_hsa_circ_65798,RMVar_hsa_circ_291925,RMVar_hsa_circ_364347,RMVar_hsa_circ_348169,RMVar_hsa_circ_271027,RMVar_hsa_circ_59297,RMVar_hsa_circ_346721,RMVar_hsa_circ_356886 45600 RMVar_ID_45600 Human_SNP_ID_77636523 A-to-I Human chr2 + 73521629 73521629 73521629 AAAAATAGCCGGACACTGTGGCGGGTGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGG AAAAATAGCCGGACACTGTGGCGGGTGCCTGTTGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGG A T ALMS1 Ensembl:ENSG00000116127 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1178416446 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2627,RMVar_hsa_circ_363390,RMVar_hsa_circ_65798,RMVar_hsa_circ_364347,RMVar_hsa_circ_348169,RMVar_hsa_circ_59297,RMVar_hsa_circ_24066,RMVar_hsa_circ_64287,RMVar_hsa_circ_376441,RMVar_hsa_circ_69522,RMVar_hsa_circ_80133,RMVar_hsa_circ_311178,RMVar_hsa_circ_361113,RMVar_hsa_circ_201231,RMVar_hsa_circ_201232 45601 RMVar_ID_45601 Human_SNP_ID_77637291 A-to-I Human chr2 + 73524509 73524509 73524509 ATGGAGTCTTGCTCTGTCACCCAGGCTGGAGTACAGTGGCATGATCTCAGCTCACTGCAACCTCT ATGGAGTCTTGCTCTGTCACCCAGGCTGGAGTGCAGTGGCATGATCTCAGCTCACTGCAACCTCT A G ALMS1 Ensembl:ENSG00000116127 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1235517683 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2627,RMVar_hsa_circ_363390,RMVar_hsa_circ_65798,RMVar_hsa_circ_364347,RMVar_hsa_circ_348169,RMVar_hsa_circ_59297,RMVar_hsa_circ_24066,RMVar_hsa_circ_64287,RMVar_hsa_circ_376441,RMVar_hsa_circ_69522,RMVar_hsa_circ_80133,RMVar_hsa_circ_311178,RMVar_hsa_circ_361113,RMVar_hsa_circ_201231,RMVar_hsa_circ_201232 45602 RMVar_ID_45602 Human_SNP_ID_77637293 A-to-I Human chr2 + 73524520 73524520 73524520 CTCTGTCACCCAGGCTGGAGTACAGTGGCATGATCTCAGCTCACTGCAACCTCTGCCTCCTTGGT CTCTGTCACCCAGGCTGGAGTACAGTGGCATGGTCTCAGCTCACTGCAACCTCTGCCTCCTTGGT A G ALMS1 Ensembl:ENSG00000116127 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs994992250 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2627,RMVar_hsa_circ_363390,RMVar_hsa_circ_65798,RMVar_hsa_circ_364347,RMVar_hsa_circ_348169,RMVar_hsa_circ_59297,RMVar_hsa_circ_24066,RMVar_hsa_circ_64287,RMVar_hsa_circ_376441,RMVar_hsa_circ_69522,RMVar_hsa_circ_80133,RMVar_hsa_circ_311178,RMVar_hsa_circ_361113,RMVar_hsa_circ_201231,RMVar_hsa_circ_201232 45603 RMVar_ID_45603 Human_SNP_ID_77637310 A-to-I Human chr2 + 73524582 73524582 73524582 GGTTCAAGCAATTCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCACCCGCCACCACGCCTG GGTTCAAGCAATTCTGCCTCAGCCTCCTGAGTGGCTGGGATTACAGGCACCCGCCACCACGCCTG A G ALMS1 Ensembl:ENSG00000116127 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1399279875 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2627,RMVar_hsa_circ_363390,RMVar_hsa_circ_65798,RMVar_hsa_circ_364347,RMVar_hsa_circ_348169,RMVar_hsa_circ_59297,RMVar_hsa_circ_24066,RMVar_hsa_circ_64287,RMVar_hsa_circ_376441,RMVar_hsa_circ_69522,RMVar_hsa_circ_80133,RMVar_hsa_circ_311178,RMVar_hsa_circ_361113,RMVar_hsa_circ_201231,RMVar_hsa_circ_201232 45604 RMVar_ID_45604 Human_SNP_ID_77637335 A-to-I Human chr2 + 73524653 73524653 73524653 TTTTGTATTTTTAGTAGAGAAAGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGATCT TTTTGTATTTTTAGTAGAGAAAGGGTTTCACCTTGTTGGCCAGGCTGGTCTCGAACTCCTGATCT A T ALMS1 Ensembl:ENSG00000116127 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs568587752 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2627,RMVar_hsa_circ_363390,RMVar_hsa_circ_65798,RMVar_hsa_circ_364347,RMVar_hsa_circ_348169,RMVar_hsa_circ_59297,RMVar_hsa_circ_24066,RMVar_hsa_circ_64287,RMVar_hsa_circ_376441,RMVar_hsa_circ_69522,RMVar_hsa_circ_80133,RMVar_hsa_circ_311178,RMVar_hsa_circ_361113,RMVar_hsa_circ_201231,RMVar_hsa_circ_201232 45605 RMVar_ID_45605 Human_SNP_ID_77637339 A-to-I Human chr2 + 73524662 73524662 73524662 TTTAGTAGAGAAAGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGATCTCAAGTGATC TTTAGTAGAGAAAGGGTTTCACCATGTTGGCCGGGCTGGTCTCGAACTCCTGATCTCAAGTGATC A G ALMS1 Ensembl:ENSG00000116127 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs999489531 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2627,RMVar_hsa_circ_363390,RMVar_hsa_circ_65798,RMVar_hsa_circ_364347,RMVar_hsa_circ_348169,RMVar_hsa_circ_59297,RMVar_hsa_circ_24066,RMVar_hsa_circ_64287,RMVar_hsa_circ_376441,RMVar_hsa_circ_69522,RMVar_hsa_circ_80133,RMVar_hsa_circ_311178,RMVar_hsa_circ_361113,RMVar_hsa_circ_201231,RMVar_hsa_circ_201232 45606 RMVar_ID_45606 Human_SNP_ID_77637340 A-to-I Human chr2 + 73524662 73524662 73524662 TTTAGTAGAGAAAGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGATCTCAAGTGATC TTTAGTAGAGAAAGGGTTTCACCATGTTGGCCTGGCTGGTCTCGAACTCCTGATCTCAAGTGATC A T ALMS1 Ensembl:ENSG00000116127 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs999489531 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2627,RMVar_hsa_circ_363390,RMVar_hsa_circ_65798,RMVar_hsa_circ_364347,RMVar_hsa_circ_348169,RMVar_hsa_circ_59297,RMVar_hsa_circ_24066,RMVar_hsa_circ_64287,RMVar_hsa_circ_376441,RMVar_hsa_circ_69522,RMVar_hsa_circ_80133,RMVar_hsa_circ_311178,RMVar_hsa_circ_361113,RMVar_hsa_circ_201231,RMVar_hsa_circ_201232 45607 RMVar_ID_45607 Human_SNP_ID_77695073 A-to-I Human chr2 - 73733397 73733349 73733398 AAAAGTAGCTGGGTGTGGTGGTGTGTGCTGGTAGTCCCAGCTACTCGGGAGGCTGAGGCACAAGA AAAAGTAGCTGGGTGTGGTGGTGTGTGCTGG__________________________________ CCCAGGTTCAAATGATTCTTGTGCCTCAGCCTCCCGAGTAGCTGGGACTA C TPRKB Ensembl:ENSG00000144034 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1204483536 Functional Loss DEL dbSNP153 32..65 33 - - - 45608 RMVar_ID_45608 Human_SNP_ID_77697923 A-to-I Human chr2 - 73743866 73743866 73743866 CTGGCTCACTGCAACCTCTGCCTGCTGGTTTCAAGCGATTCTCCTGCCTTAGCCTCCCGAGTAGC CTGGCTCACTGCAACCTCTGCCTGCTGGTTTCCAGCGATTCTCCTGCCTTAGCCTCCCGAGTAGC T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs964556110 Functional Loss SNV dbSNP153 33..33 33 - - - 45609 RMVar_ID_45609 Human_SNP_ID_77702979 A-to-I Human chr2 - 73764411 73764411 73764411 CATTGCCATTTTTAGGCCAGGTGCATTGGCTCACACCTGTAATCCCAGCACTTAGGGAGGCCAAG CATTGCCATTTTTAGGCCAGGTGCATTGGCTCGCACCTGTAATCCCAGCACTTAGGGAGGCCAAG T C DUSP11 Ensembl:ENSG00000144048 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1050438320 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87785,RMVar_hsa_circ_93127,RMVar_hsa_circ_201251,RMVar_hsa_circ_201252 45610 RMVar_ID_45610 Human_SNP_ID_77720385 A-to-I Human chr2 + 73845731 73845731 73845731 TCAGCTCACTGCAACCTCTGCCTCCCCGACTCAAGTGATTCTCCTACCTCAGCCTCCCGAGTGAC TCAGCTCACTGCAACCTCTGCCTCCCCGACTCCAGTGATTCTCCTACCTCAGCCTCCCGAGTGAC A C STAMBP Ensembl:ENSG00000124356 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1369058901 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69213,RMVar_hsa_circ_42440,RMVar_hsa_circ_316202,RMVar_hsa_circ_201254,RMVar_hsa_circ_331813,RMVar_hsa_circ_320298,RMVar_hsa_circ_73807,RMVar_hsa_circ_201255,RMVar_hsa_circ_313998,RMVar_hsa_circ_70321,RMVar_hsa_circ_201258 45611 RMVar_ID_45611 Human_SNP_ID_77720609 A-to-I Human chr2 + 73846589 73846589 73846589 ATTGAGGCTGCAGTGAGCCATGATTGACCACTACAGTCCAGCCTAGGTGACAGAGTGAGACTCTC ATTGAGGCTGCAGTGAGCCATGATTGACCACTGCAGTCCAGCCTAGGTGACAGAGTGAGACTCTC A G STAMBP Ensembl:ENSG00000124356 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1463309647 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9997103,Human_RBP_ID_25565051 RMVar_hsa_circ_69213,RMVar_hsa_circ_42440,RMVar_hsa_circ_316202,RMVar_hsa_circ_201254,RMVar_hsa_circ_331813,RMVar_hsa_circ_320298,RMVar_hsa_circ_73807,RMVar_hsa_circ_201255,RMVar_hsa_circ_313998,RMVar_hsa_circ_70321,RMVar_hsa_circ_201258 45612 RMVar_ID_45612 Human_SNP_ID_77764854 A-to-I Human chr2 + 74018071 74018071 74018071 CTCACTGCAACCTCCTCCTCCCGGATTCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGG CTCACTGCAACCTCCTCCTCCCGGATTCAAGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGG A C TET3 Ensembl:ENSG00000187605 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1483013313 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_315910 45613 RMVar_ID_45613 Human_SNP_ID_77783149 A-to-I Human chr2 + 74086875 74086875 74086875 AACCATTTTTCAGTGTACAGGTTGGTGGCATTAAGTACATTCACGTTGTTGTACAAGCATCAACC AACCATTTTTCAGTGTACAGGTTGGTGGCATTCAGTACATTCACGTTGTTGTACAAGCATCAACC A C TET3 Ensembl:ENSG00000187605 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1407381762 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_46049,RMVar_hsa_circ_269178,RMVar_hsa_circ_52572,RMVar_hsa_circ_348126,RMVar_hsa_circ_89843,RMVar_hsa_circ_11625,RMVar_hsa_circ_14242,RMVar_hsa_circ_201281 45614 RMVar_ID_45614 Human_SNP_ID_77783158 A-to-I Human chr2 + 74086895 74086895 74086895 GTTGGTGGCATTAAGTACATTCACGTTGTTGTACAAGCATCAACCTAGTCTATTTCCAGAACTTT GTTGGTGGCATTAAGTACATTCACGTTGTTGTTCAAGCATCAACCTAGTCTATTTCCAGAACTTT A T TET3 Ensembl:ENSG00000187605 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1201874734 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_46049,RMVar_hsa_circ_269178,RMVar_hsa_circ_52572,RMVar_hsa_circ_348126,RMVar_hsa_circ_89843,RMVar_hsa_circ_11625,RMVar_hsa_circ_14242,RMVar_hsa_circ_201281 45615 RMVar_ID_45615 Human_SNP_ID_77783205 A-to-I Human chr2 + 74087072 74087070 74087072 CTGGGTGTCTCATGTCAGTGGAATCATGTACTATGTGTCCTTTTGTGTCTGGCTTATTTCACATA CTGGGTGTCTCATGTCAGTGGAATCATGTAC__TGTGTCCTTTTGTGTCTGGCTTATTTCACATA CTA C TET3 Ensembl:ENSG00000187605 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1319236843 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_3634364 RMVar_hsa_circ_46049,RMVar_hsa_circ_269178,RMVar_hsa_circ_52572,RMVar_hsa_circ_348126,RMVar_hsa_circ_89843,RMVar_hsa_circ_11625,RMVar_hsa_circ_14242,RMVar_hsa_circ_201281 45616 RMVar_ID_45616 Human_SNP_ID_77793344 A-to-I Human chr2 + 74122659 74122658 74122660 CCTCAGCCTCCCAAGTAGCTGGGACTAAAGGCATGTGCCACTACACCTAGCTTTTTTTTTTTTTT CCTCAGCCTCCCAAGTAGCTGGGACTAAAGGC__GTGCCACTACACCTAGCTTTTTTTTTTTTTT CAT C FNBP1P1 Ensembl:ENSG00000257800 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1487553623 Functional Loss DEL dbSNP153 33..34 33 - - - 45617 RMVar_ID_45617 Human_SNP_ID_77793345 A-to-I Human chr2 + 74122659 74122659 74122659 CCTCAGCCTCCCAAGTAGCTGGGACTAAAGGCATGTGCCACTACACCTAGCTTTTTTTTTTTTTT CCTCAGCCTCCCAAGTAGCTGGGACTAAAGGCGTGTGCCACTACACCTAGCTTTTTTTTTTTTTT A G FNBP1P1 Ensembl:ENSG00000257800 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1456520999 Functional Loss SNV dbSNP153 33..33 33 - - - 45618 RMVar_ID_45618 Human_SNP_ID_77803507 A-to-I Human chr2 - 74161586 74161586 74161586 GGAGTGCAGTGGCATGATCTCAGCACACTGCAAGCTCCGCCTCCCGGGTTCACGCCATTCTGCCA GGAGTGCAGTGGCATGATCTCAGCACACTGCAGGCTCCGCCTCCCGGGTTCACGCCATTCTGCCA T C MOB1A Ensembl:ENSG00000114978 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1214485250 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78127,RMVar_hsa_circ_201284,RMVar_hsa_circ_201286,RMVar_hsa_circ_201287,RMVar_hsa_circ_310993,RMVar_hsa_circ_201289,RMVar_hsa_circ_292873,RMVar_hsa_circ_201288 45619 RMVar_ID_45619 Human_SNP_ID_77805333 A-to-I Human chr2 - 74169257 74169257 74169257 CCTCAAGTGATCCGCCTGCCTCATCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCACC CCTCAAGTGATCCGCCTGCCTCATCCTCCCAAGGTGCTGGGATTACAGGCGTGAGCCACTGCACC T C MOB1A Ensembl:ENSG00000114978 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs577490363 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78127,RMVar_hsa_circ_201284,RMVar_hsa_circ_110470,RMVar_hsa_circ_201286,RMVar_hsa_circ_201287,RMVar_hsa_circ_292873,RMVar_hsa_circ_201288,RMVar_hsa_circ_328232,RMVar_hsa_circ_277501,RMVar_hsa_circ_201291,RMVar_hsa_circ_201292,RMVar_hsa_circ_107261,RMVar_hsa_circ_287920,RMVar_hsa_circ_201294,RMVar_hsa_circ_201295 45620 RMVar_ID_45620 Human_SNP_ID_77805369 A-to-I Human chr2 - 74169402 74169396 74169402 TGCCTCCTGGCTTCAAGCAGTTCTCCCACCTCAGTCTCCAGAGTAGCTGGGATTACAGGCATGTG TGCCTCCTGGCTTCAAGCAGTTCTCCCACCTC______CAGAGTAGCTGGGATTACAGGCATGTG GGAGACT G MOB1A Ensembl:ENSG00000114978 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1353933040 Functional Loss DEL dbSNP153 33..38 33 - - - RMVar_hsa_circ_78127,RMVar_hsa_circ_201284,RMVar_hsa_circ_110470,RMVar_hsa_circ_201286,RMVar_hsa_circ_201287,RMVar_hsa_circ_292873,RMVar_hsa_circ_201288,RMVar_hsa_circ_328232,RMVar_hsa_circ_277501,RMVar_hsa_circ_201291,RMVar_hsa_circ_201292,RMVar_hsa_circ_107261,RMVar_hsa_circ_287920,RMVar_hsa_circ_201294,RMVar_hsa_circ_201295 45621 RMVar_ID_45621 Human_SNP_ID_77805371 A-to-I Human chr2 - 74169402 74169402 74169402 TGCCTCCTGGCTTCAAGCAGTTCTCCCACCTCAGTCTCCAGAGTAGCTGGGATTACAGGCATGTG TGCCTCCTGGCTTCAAGCAGTTCTCCCACCTCCGTCTCCAGAGTAGCTGGGATTACAGGCATGTG T G MOB1A Ensembl:ENSG00000114978 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1338516909 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78127,RMVar_hsa_circ_201284,RMVar_hsa_circ_110470,RMVar_hsa_circ_201286,RMVar_hsa_circ_201287,RMVar_hsa_circ_292873,RMVar_hsa_circ_201288,RMVar_hsa_circ_328232,RMVar_hsa_circ_277501,RMVar_hsa_circ_201291,RMVar_hsa_circ_201292,RMVar_hsa_circ_107261,RMVar_hsa_circ_287920,RMVar_hsa_circ_201294,RMVar_hsa_circ_201295 45622 RMVar_ID_45622 Human_SNP_ID_77805478 A-to-I Human chr2 - 74169837 74169837 74169837 ATCACTTGAGGTCAGGAGTTCGAGACCAGCCTAGGCAACATGGTGAAACACCAGCTCTACTAAAA ATCACTTGAGGTCAGGAGTTCGAGACCAGCCTCGGCAACATGGTGAAACACCAGCTCTACTAAAA T G MOB1A Ensembl:ENSG00000114978 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1461256651 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78127,RMVar_hsa_circ_201284,RMVar_hsa_circ_110470,RMVar_hsa_circ_201286,RMVar_hsa_circ_201287,RMVar_hsa_circ_292873,RMVar_hsa_circ_201288,RMVar_hsa_circ_328232,RMVar_hsa_circ_277501,RMVar_hsa_circ_201291,RMVar_hsa_circ_201292,RMVar_hsa_circ_107261,RMVar_hsa_circ_287920,RMVar_hsa_circ_201294,RMVar_hsa_circ_201295 45623 RMVar_ID_45623 Human_SNP_ID_77805612 A-to-I Human chr2 - 74170343 74170343 74170343 CACGAGGTCAGGAGATTGAGACCATCCTGGCCAACATGGTAAAACCCCATCTCTACTAAAAATAC CACGAGGTCAGGAGATTGAGACCATCCTGGCCGACATGGTAAAACCCCATCTCTACTAAAAATAC T C MOB1A Ensembl:ENSG00000114978 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs536493892 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78127,RMVar_hsa_circ_201284,RMVar_hsa_circ_110470,RMVar_hsa_circ_201286,RMVar_hsa_circ_201287,RMVar_hsa_circ_292873,RMVar_hsa_circ_201288,RMVar_hsa_circ_328232,RMVar_hsa_circ_277501,RMVar_hsa_circ_201291,RMVar_hsa_circ_201292,RMVar_hsa_circ_107261,RMVar_hsa_circ_287920,RMVar_hsa_circ_201294,RMVar_hsa_circ_201295 45624 RMVar_ID_45624 Human_SNP_ID_77805690 A-to-I Human chr2 - 74170569 74170569 74170569 CACCACACCTGGCTAATTTTTCTATTTTTAGTAGAGACGAGGTTTTGCCATGTTAGCCAGGCTGG CACCACACCTGGCTAATTTTTCTATTTTTAGTGGAGACGAGGTTTTGCCATGTTAGCCAGGCTGG T C MOB1A Ensembl:ENSG00000114978 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1249763181 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78127,RMVar_hsa_circ_201284,RMVar_hsa_circ_110470,RMVar_hsa_circ_201286,RMVar_hsa_circ_201287,RMVar_hsa_circ_292873,RMVar_hsa_circ_201288,RMVar_hsa_circ_328232,RMVar_hsa_circ_277501,RMVar_hsa_circ_201291,RMVar_hsa_circ_201292,RMVar_hsa_circ_107261,RMVar_hsa_circ_287920,RMVar_hsa_circ_201294,RMVar_hsa_circ_201295 45625 RMVar_ID_45625 Human_SNP_ID_77815976 A-to-I Human chr2 + 74207702 74207702 74207702 AAAATTTTTTTAACCTCAAAATTTCTTATAATAGGAATCAACAGTGAGACAATTATGAAACCAGC AAAATTTTTTTAACCTCAAAATTTCTTATAATGGGAATCAACAGTGAGACAATTATGAAACCAGC A G MTHFD2 Ensembl:ENSG00000065911 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1303895971 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13965663 RMVar_hsa_circ_24236,RMVar_hsa_circ_39818,RMVar_hsa_circ_84324,RMVar_hsa_circ_201296,RMVar_hsa_circ_29826,RMVar_hsa_circ_11859,RMVar_hsa_circ_323806,RMVar_hsa_circ_337956,RMVar_hsa_circ_24330,RMVar_hsa_circ_47509,RMVar_hsa_circ_349359 45626 RMVar_ID_45626 Human_SNP_ID_77869772 A-to-I Human chr2 + 74418300 74418300 74418300 CCCGAGGTCTCTTAGGTGTTGGCACTTCGCTGAGCTCCTTCTGACTCCCTACCAGCGCTGTCCTG CCCGAGGTCTCTTAGGTGTTGGCACTTCGCTGGGCTCCTTCTGACTCCCTACCAGCGCTGTCCTG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956708866 Functional Loss SNV dbSNP153 33..33 33 - - - 45627 RMVar_ID_45627 Human_SNP_ID_77884372 A-to-I Human chr2 - 74468245 74468245 74468245 GCCAGGCTGGTCAGGAACTCCTGACCTCAAGTAATCCACCCTCCTTGGCCTCCCGAAGTGCTAGG GCCAGGCTGGTCAGGAACTCCTGACCTCAAGTGATCCACCCTCCTTGGCCTCCCGAAGTGCTAGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1236534314 Functional Loss SNV dbSNP153 33..33 33 - - - 45628 RMVar_ID_45628 Human_SNP_ID_77887899 A-to-I Human chr2 - 74479705 74479705 74479705 CCTGTACTCCCAGCTACTTGGGAGGCTGAGGCAAGAGGATCGTTTGAGCCCAGGAGGTCAAGGCT CCTGTACTCCCAGCTACTTGGGAGGCTGAGGCGAGAGGATCGTTTGAGCCCAGGAGGTCAAGGCT T C CCDC142 Ensembl:ENSG00000135637 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1056752677 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569760,Human_RBP_ID_25565896 RMVar_hsa_circ_123872,RMVar_hsa_circ_201358,RMVar_hsa_circ_39360,RMVar_hsa_circ_81450,RMVar_hsa_circ_201359,RMVar_hsa_circ_54840 45629 RMVar_ID_45629 Human_SNP_ID_77890452 A-to-I Human chr2 + 74488075 74488075 74488075 TAGTTCACTGCAGCCTTGAACTCCTGGGCTCAAACAGTCCTTCGATTTCAGCCTCCCGAGTAGCT TAGTTCACTGCAGCCTTGAACTCCTGGGCTCAGACAGTCCTTCGATTTCAGCCTCCCGAGTAGCT A G TTC31 Ensembl:ENSG00000115282 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs983157747 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108901,RMVar_hsa_circ_201362 45630 RMVar_ID_45630 Human_SNP_ID_77896587 A-to-I Human chr2 - 74510213 74510213 74510213 TTTTGTACTTTTTGTAGTGACGGAGTCCCACCATGTTGCCCAGGCTGGTCTCCAACTCCTGGGCT TTTTGTACTTTTTGTAGTGACGGAGTCCCACCCTGTTGCCCAGGCTGGTCTCCAACTCCTGGGCT T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1386371919 Functional Loss SNV dbSNP153 33..33 33 - - - 45631 RMVar_ID_45631 Human_SNP_ID_77944901 A-to-I Human chr2 + 74709043 74709043 74709043 CAAAAAGAGCTGGTGTGGTGGTGCGTGCCTATAGTCCCAGCTAACTCAGGAGGATGAGGTGGGAG CAAAAAGAGCTGGTGTGGTGGTGCGTGCCTATGGTCCCAGCTAACTCAGGAGGATGAGGTGGGAG A G HSALNG0016087 RNACentral:URS0000EAE73D lincRNA exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs929925543 Functional Loss SNV dbSNP153 33..33 33 - - - 45632 RMVar_ID_45632 Human_SNP_ID_77945224 A-to-I Human chr2 + 74710599 74710599 74710599 CATATCGGCCAGGCATGGTGGCTCACGCCTGTAATCCCAGCACTCTGGGAGGCTGAGGCAGGCAG CATATCGGCCAGGCATGGTGGCTCACGCCTGTCATCCCAGCACTCTGGGAGGCTGAGGCAGGCAG A C HSALNG0016087 RNACentral:URS0000EAE73D lincRNA exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1378537278 Functional Loss SNV dbSNP153 33..33 33 - - - 45633 RMVar_ID_45633 Human_SNP_ID_77945526 A-to-I Human chr2 + 74711788 74711788 74711788 GGGACTACAGGCGCACACTGCCGTGCCTGGCTAATTTTTTGTGTTTTAGTAGAGATGGGGTTTCA GGGACTACAGGCGCACACTGCCGTGCCTGGCTGATTTTTTGTGTTTTAGTAGAGATGGGGTTTCA A G HSALNG0016087 RNACentral:URS0000EAE73D lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs757457892 Functional Loss SNV dbSNP153 33..33 33 - - - 45634 RMVar_ID_45634 Human_SNP_ID_77999360 A-to-I Human chr2 - 74923929 74923929 74923929 AAAAAGCAAGGGGTGATCGGGCATGGTGGCTCACGCCTCTAATCCCAGCACTTTGGGAGGCTGAG AAAAAGCAAGGGGTGATCGGGCATGGTGGCTCTCGCCTCTAATCCCAGCACTTTGGGAGGCTGAG T A AC104135.1 Ensembl:ENSG00000236209 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1415951891 Functional Loss SNV dbSNP153 33..33 33 - - - 45635 RMVar_ID_45635 Human_SNP_ID_614398837 A-to-I Human chr17 - 441466 441466 441466 GTTACCGAGCACTGTAAGCTCAGCTCGGCTGTAGCTCCGGGTTTCTGCCGATGGCCTCCATCTGC GTTACCGAGCACTGTAAGCTCAGCTCGGCTGTCGCTCCGGGTTTCTGCCGATGGCCTCCATCTGC T G RFLNB Ensembl:ENSG00000183688 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1555542808 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_486630,Human_RBP_ID_4417298,Human_RBP_ID_6579246,Human_RBP_ID_12956960,Human_RBP_ID_22499120,Human_RBP_ID_26456956 RMVar_hsa_circ_83328,RMVar_hsa_circ_180889,RMVar_hsa_circ_79618,RMVar_hsa_circ_180890 45636 RMVar_ID_45636 Human_SNP_ID_614408370 A-to-I Human chr17 - 516429 516429 516429 CCGGGAGGCAAAGATTGCAGTGAGCCGAGATCACGCCACTGCACTCCAGCCTGGCGACAGAGTGA CCGGGAGGCAAAGATTGCAGTGAGCCGAGATCGCGCCACTGCACTCCAGCCTGGCGACAGAGTGA T C VPS53 Ensembl:ENSG00000141252 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1326272959 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25286981 RMVar_hsa_circ_267135 45637 RMVar_ID_45637 Human_SNP_ID_614408696 A-to-I Human chr17 - 517618 517618 517618 CTACTGGGGAGGCTGAGGCAGGAGAATCACTTAAACCCGGGAGGTGGAGGCTGCAGTGAGCCAAG CTACTGGGGAGGCTGAGGCAGGAGAATCACTTGAACCCGGGAGGTGGAGGCTGCAGTGAGCCAAG T C VPS53 Ensembl:ENSG00000141252 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1139888 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267135 45638 RMVar_ID_45638 Human_SNP_ID_614408706 A-to-I Human chr17 - 517658 517658 517658 AAAATTAGCCGGGTGTCATGGCGAGTGCCTGTAATCCCAGCTACTGGGGAGGCTGAGGCAGGAGA AAAATTAGCCGGGTGTCATGGCGAGTGCCTGTGATCCCAGCTACTGGGGAGGCTGAGGCAGGAGA T C VPS53 Ensembl:ENSG00000141252 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs977946573 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267135 45639 RMVar_ID_45639 Human_SNP_ID_614408973 A-to-I Human chr17 - 518647 518647 518647 TTCTCCTGCCTCAGCCTCCTGAGTATCGGATTACAGGCGTGAGCCACCGAGCCCAGCCCCTTCCT TTCTCCTGCCTCAGCCTCCTGAGTATCGGATTGCAGGCGTGAGCCACCGAGCCCAGCCCCTTCCT T C VPS53 Ensembl:ENSG00000141252 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1425011040 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20219013,Human_RBP_ID_26456960,Human_RBP_ID_27452874 RMVar_hsa_circ_267135 45640 RMVar_ID_45640 Human_SNP_ID_614427807 A-to-I Human chr17 - 584772 584772 584772 CCTGTAATCCCAGCACTTTGGGAGGCCAAGGTAGGAGGAGCTCTTGAGCCCAGGATTCAAGACCA CCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGAGGAGCTCTTGAGCCCAGGATTCAAGACCA T C VPS53 Ensembl:ENSG00000141252 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968948341 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 45641 RMVar_ID_45641 Human_SNP_ID_614448808 A-to-I Human chr17 - 657201 657201 657201 GAGACCAAGTACAAGTTGTGCAAAGTGAGAAAAATCTTTGTGGGCACAAAAGGAATCCCTCATCT GAGACCAAGTACAAGTTGTGCAAAGTGAGAAAGATCTTTGTGGGCACAAAAGGAATCCCTCATCT T C RPS4XP17,VPS53 Ensembl:ENSG00000244097,Ensembl:ENSG00000141252 Pseudogene,Protein coding exon,intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs879060493 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_180923,RMVar_hsa_circ_180922,RMVar_hsa_circ_180920 45642 RMVar_ID_45642 Human_SNP_ID_614455168 A-to-I Human chr17 - 677999 677999 677999 CTCCCACCTCAGCCTCCTGAGTAGCTGGGACTACAGGCACTCGCCACCACGCCTGGCTAATTTTT CTCCCACCTCAGCCTCCTGAGTAGCTGGGACTGCAGGCACTCGCCACCACGCCTGGCTAATTTTT T C VPS53 Ensembl:ENSG00000141252 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1173452751 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25064,RMVar_hsa_circ_297553,RMVar_hsa_circ_378804,RMVar_hsa_circ_337370,RMVar_hsa_circ_180914,RMVar_hsa_circ_180913,RMVar_hsa_circ_180921,RMVar_hsa_circ_267512,RMVar_hsa_circ_307035,RMVar_hsa_circ_318465,RMVar_hsa_circ_180920 45643 RMVar_ID_45643 Human_SNP_ID_614465486 A-to-I Human chr17 + 717003 717003 717003 TAGCTGGCCGTGGTGGTGCACAGAATCACTTGAACCCGAGAGGTGGAGGTTGCAGTGAGCCAAGA TAGCTGGCCGTGGTGGTGCACAGAATCACTTGGACCCGAGAGGTGGAGGTTGCAGTGAGCCAAGA A G RF00017-1784,lnc-FAM57A-5 RNACentral:URS0000904F64,RNACentral:URS00008B707C SRP RNA,lincRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1302365094 Functional Loss SNV dbSNP153 33..33 33 - - - 45644 RMVar_ID_45644 Human_SNP_ID_614468001 A-to-I Human chr17 - 725164 725164 725164 ACAAAAACATTTAAAAATTATCCAGGTGCGGTAGCATGTGCCTGCAGTCCTGGCTACATGGGAAG ACAAAAACATTTAAAAATTATCCAGGTGCGGTGGCATGTGCCTGCAGTCCTGGCTACATGGGAAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1254561804 Functional Loss SNV dbSNP153 33..33 33 - - - 45645 RMVar_ID_45645 Human_SNP_ID_614472197 A-to-I Human chr17 + 738279 738279 738279 CACCACGCCCGGCTAATGTTTGTATTTTTAGTAGAGATGGGGTTTTGCCATGTTGGCCAGGCTGA CACCACGCCCGGCTAATGTTTGTATTTTTAGTGGAGATGGGGTTTTGCCATGTTGGCCAGGCTGA A G TLCD3A Ensembl:ENSG00000167695 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs990172258 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99093,RMVar_hsa_circ_180929 45646 RMVar_ID_45646 Human_SNP_ID_614485436 A-to-I Human chr17 - 780631 780631 780631 TCACACCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACCACAGGCGCGTACCACAACACCCG TCACACCATTCTCCTGCCTCAGCCTCCCGAGTGGCTGGGACCACAGGCGCGTACCACAACACCCG T C GLOD4 Ensembl:ENSG00000167699 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490832,GSM3490833,GSM3490834 Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 31158229,32596459 RNA-Seq:(High) rs1432604753 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82792,RMVar_hsa_circ_180935,RMVar_hsa_circ_180937 45647 RMVar_ID_45647 Human_SNP_ID_614527067 A-to-I Human chr17 - 907615 907615 907615 TATTTCAGACCAGGCACAGTGTTTTCACGCCTATAATGTCAGGACTTTGGGAGGCCAAGGCGGGA TATTTCAGACCAGGCACAGTGTTTTCACGCCTGTAATGTCAGGACTTTGGGAGGCCAAGGCGGGA T C NXN Ensembl:ENSG00000167693 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444351339 Functional Loss SNV dbSNP153 33..33 33 - - - 45648 RMVar_ID_45648 Human_SNP_ID_614531436 A-to-I Human chr17 - 920887 920887 920887 AAAACCCCGTCTTTACTAAAATTACAAAAATTAGCCGGACATGGTGGCGGGCGCCTGTAATCCCA AAAACCCCGTCTTTACTAAAATTACAAAAATTGGCCGGACATGGTGGCGGGCGCCTGTAATCCCA T C NXN Ensembl:ENSG00000167693 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs550840495 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13214190 45649 RMVar_ID_45649 Human_SNP_ID_614546697 A-to-I Human chr17 - 968885 968885 968885 TCTCCCAGGCTGGAGTGCAGTGGTACGATCTCAGCTCACTGTGACCTCTGCCTCTTAGGTTCAAG TCTCCCAGGCTGGAGTGCAGTGGTACGATCTCCGCTCACTGTGACCTCTGCCTCTTAGGTTCAAG T G NXN Ensembl:ENSG00000167693 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1387824698 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13218115 45650 RMVar_ID_45650 Human_SNP_ID_614584719 A-to-I Human chr17 - 1084931 1084931 1084931 AGGCGTGGTGGCGGGCGCCTGTAACGCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCCCTTGAA AGGCGTGGTGGCGGGCGCCTGTAACGCCAGCTGCTCGGGAGGCTGAGGCAGGAGAATCCCTTGAA T C ABR Ensembl:ENSG00000159842 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1365440272 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50633,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_31588,RMVar_hsa_circ_180966,RMVar_hsa_circ_327226,RMVar_hsa_circ_114450,RMVar_hsa_circ_180969,RMVar_hsa_circ_180970,RMVar_hsa_circ_41752,RMVar_hsa_circ_362855,RMVar_hsa_circ_291936,RMVar_hsa_circ_180971,RMVar_hsa_circ_180972 45651 RMVar_ID_45651 Human_SNP_ID_614585914 A-to-I Human chr17 - 1088771 1088771 1088771 CAGCTTGGCCAACATGGTGAAACCCCGTTTCTACTAAAAATACAAAAATTAGCCGGGCATGATAA CAGCTTGGCCAACATGGTGAAACCCCGTTTCTGCTAAAAATACAAAAATTAGCCGGGCATGATAA T C ABR Ensembl:ENSG00000159842 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs746487999 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50633,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_31588,RMVar_hsa_circ_180966,RMVar_hsa_circ_327226,RMVar_hsa_circ_114450,RMVar_hsa_circ_180969,RMVar_hsa_circ_180970,RMVar_hsa_circ_41752,RMVar_hsa_circ_362855,RMVar_hsa_circ_291936,RMVar_hsa_circ_180971,RMVar_hsa_circ_180972 45652 RMVar_ID_45652 Human_SNP_ID_614605655 A-to-I Human chr17 - 1152970 1152970 1152970 ATTCTCCTGCCTCAGCCCAAGTAGCTGGGACTACAGGCGTGCACCACCATGCCTGGCTAATTTTG ATTCTCCTGCCTCAGCCCAAGTAGCTGGGACTTCAGGCGTGCACCACCATGCCTGGCTAATTTTG T A ABR Ensembl:ENSG00000159842 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs900004885 Functional Loss SNV dbSNP153 33..33 33 - - - 45653 RMVar_ID_45653 Human_SNP_ID_614622200 A-to-I Human chr17 - 1205183 1205183 1205183 AATAATGGGGATAAAACCGGGTATGGTGGCTCAGGCCTGCAATCCCAGCACTTTGGGAGGCTGAG AATAATGGGGATAAAACCGGGTATGGTGGCTCTGGCCTGCAATCCCAGCACTTTGGGAGGCTGAG T A ABR Ensembl:ENSG00000159842 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1344880051 Functional Loss SNV dbSNP153 33..33 33 - - - 45654 RMVar_ID_45654 Human_SNP_ID_614636723 A-to-I Human chr17 - 1251061 1251061 1251061 AAAATTAGCCCGGCGTGGTGGCGGACGCCTGTAGTCCCAGCTACTCGGGAGGCGGAGGCAGGAGA AAAATTAGCCCGGCGTGGTGGCGGACGCCTGTGGTCCCAGCTACTCGGGAGGCGGAGGCAGGAGA T C AC144836.1 Ensembl:ENSG00000262213 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1306469386 Functional Loss SNV dbSNP153 33..33 33 - - - 45655 RMVar_ID_45655 Human_SNP_ID_614636724 A-to-I Human chr17 - 1251061 1251061 1251061 AAAATTAGCCCGGCGTGGTGGCGGACGCCTGTAGTCCCAGCTACTCGGGAGGCGGAGGCAGGAGA AAAATTAGCCCGGCGTGGTGGCGGACGCCTGTCGTCCCAGCTACTCGGGAGGCGGAGGCAGGAGA T G AC144836.1 Ensembl:ENSG00000262213 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1306469386 Functional Loss SNV dbSNP153 33..33 33 - - - 45656 RMVar_ID_45656 Human_SNP_ID_614669416 A-to-I Human chr17 - 1348811 1348811 1348811 CCCCGTGTTAACCCGGATGGTCTCAATCTCCTAACCTCGTGATCCGCCTGCCTCGGCCTCCCAAA CCCCGTGTTAACCCGGATGGTCTCAATCTCCTGACCTCGTGATCCGCCTGCCTCGGCCTCCCAAA T C YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1218329674 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12885880 RMVar_hsa_circ_93985,RMVar_hsa_circ_180978 45657 RMVar_ID_45657 Human_SNP_ID_614669549 A-to-I Human chr17 - 1349108 1349108 1349108 TCAATCTCCTAACCTCGTGATCCACCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCCCGAG TCAATCTCCTAACCTCGTGATCCACCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCCCGAG T C YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1368322930 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93985,RMVar_hsa_circ_180978 45658 RMVar_ID_45658 Human_SNP_ID_614669592 A-to-I Human chr17 - 1349219 1349219 1349219 TTCTGCCTCGTCCTCTCTGAGTTGCTGGGACTACAGGTGCCCACCACCACGCCTGGCAATAATTC TTCTGCCTCGTCCTCTCTGAGTTGCTGGGACTGCAGGTGCCCACCACCACGCCTGGCAATAATTC T C YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1236454450 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93985,RMVar_hsa_circ_180978 45659 RMVar_ID_45659 Human_SNP_ID_614669632 A-to-I Human chr17 - 1349331 1349331 1349331 TTTGTCAAAAATTAGAGTTTTTGAGATGGAGTATCACTCTGTTGCCCAGGGTGGAGTATAGTGGC TTTGTCAAAAATTAGAGTTTTTGAGATGGAGTGTCACTCTGTTGCCCAGGGTGGAGTATAGTGGC T C YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs898287749 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12885886 RMVar_hsa_circ_93985,RMVar_hsa_circ_180978 45660 RMVar_ID_45660 Human_SNP_ID_614669975 A-to-I Human chr17 - 1350227 1350226 1350227 GGTAATACGGCCTGGTGCAGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCCGAAGCGGGT GGTAATACGGCCTGGTGCAGTGGCTCACGCCT_TAATCCCAGCACTTTGGGAGGCCGAAGCGGGT AT A YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1227689068 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_93985,RMVar_hsa_circ_180978 45661 RMVar_ID_45661 Human_SNP_ID_614669976 A-to-I Human chr17 - 1350227 1350227 1350227 GGTAATACGGCCTGGTGCAGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCCGAAGCGGGT GGTAATACGGCCTGGTGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAAGCGGGT T C YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1277615968 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93985,RMVar_hsa_circ_180978 45662 RMVar_ID_45662 Human_SNP_ID_614670072 A-to-I Human chr17 - 1350570 1350570 1350570 AGGTGTGGTGGCGGGCACCTGTAATCCCTGCTACTCAGGAGGCTGAGACAGGAGAATCACTTGAA AGGTGTGGTGGCGGGCACCTGTAATCCCTGCTGCTCAGGAGGCTGAGACAGGAGAATCACTTGAA T C YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs901799111 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5186867,Human_RBP_ID_22717321 RMVar_hsa_circ_93985,RMVar_hsa_circ_180978 45663 RMVar_ID_45663 Human_SNP_ID_614670312 A-to-I Human chr17 - 1351195 1351195 1351195 CCACCACTCCTAGCTAATTTTTTGTATTTTTAATAGAGACGGGGTTCCACTATGTTGGCCAGGCT CCACCACTCCTAGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTCCACTATGTTGGCCAGGCT T C YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1244571618 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12885942 RMVar_hsa_circ_93985,RMVar_hsa_circ_180978 45664 RMVar_ID_45664 Human_SNP_ID_614670319 A-to-I Human chr17 - 1351216 1351216 1351216 TGGGACTACAGGTGTCTGCCACCACCACTCCTAGCTAATTTTTTGTATTTTTAATAGAGACGGGG TGGGACTACAGGTGTCTGCCACCACCACTCCTGGCTAATTTTTTGTATTTTTAATAGAGACGGGG T C YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1469570235 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93985,RMVar_hsa_circ_180978 45665 RMVar_ID_45665 Human_SNP_ID_614670380 A-to-I Human chr17 - 1351391 1351387 1351391 TGACTTGAAAGTTTTTTCTGTGTGTGTGTTTTATTTTTTTTTTTTGAGATGGAGTTTTGCTCTTG TGACTTGAAAGTTTTTTCTGTGTGTGTGTTTT____TTTTTTTTTGAGATGGAGTTTTGCTCTTG AAAAT A YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1399454650 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_2493346,Human_RBP_ID_3512013,Human_RBP_ID_23710864 RMVar_hsa_circ_93985,RMVar_hsa_circ_180978 45666 RMVar_ID_45666 Human_SNP_ID_614670385 A-to-I Human chr17 - 1351391 1351389 1351391 TGACTTGAAAGTTTTTTCTGTGTGTGTGTTTTATTTTTTTTTTTTGAGATGGAGTTTTGCTCTTG TGACTTGAAAGTTTTTTCTGTGTGTGTGTTTT__TTTTTTTTTTTGAGATGGAGTTTTGCTCTTG AAT A YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1480381906 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_2493346,Human_RBP_ID_3512013,Human_RBP_ID_23710864 RMVar_hsa_circ_93985,RMVar_hsa_circ_180978 45667 RMVar_ID_45667 Human_SNP_ID_614670387 A-to-I Human chr17 - 1351391 1351391 1351391 TGACTTGAAAGTTTTTTCTGTGTGTGTGTTTTATTTTTTTTTTTTGAGATGGAGTTTTGCTCTTG TGACTTGAAAGTTTTTTCTGTGTGTGTGTTTTTTTTTTTTTTTTTGAGATGGAGTTTTGCTCTTG T A YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1174792428 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2493346,Human_RBP_ID_3512013,Human_RBP_ID_23710864 RMVar_hsa_circ_93985,RMVar_hsa_circ_180978 45668 RMVar_ID_45668 Human_SNP_ID_614670388 A-to-I Human chr17 - 1351391 1351391 1351391 TGACTTGAAAGTTTTTTCTGTGTGTGTGTTTTATTTTTTTTTTTTGAGATGGAGTTTTGCTCTTG TGACTTGAAAGTTTTTTCTGTGTGTGTGTTTTGTTTTTTTTTTTTGAGATGGAGTTTTGCTCTTG T C YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1174792428 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2493346,Human_RBP_ID_3512013,Human_RBP_ID_23710864 RMVar_hsa_circ_93985,RMVar_hsa_circ_180978 45669 RMVar_ID_45669 Human_SNP_ID_614670797 A-to-I Human chr17 - 1352624 1352624 1352624 CTACTCAGGAGGCTGAGGCCGGAGAATTGCTTAAACCCAGGAGGCGGAGGTTGCAGTGAGCTGAG CTACTCAGGAGGCTGAGGCCGGAGAATTGCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCTGAG T C YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1250557416 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93985,RMVar_hsa_circ_180978 45670 RMVar_ID_45670 Human_SNP_ID_614670808 A-to-I Human chr17 - 1352650 1352650 1352650 GTGGTGGCGGGCTCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCCGGAGAATTGCTTAAACCCA GTGGTGGCGGGCTCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCCGGAGAATTGCTTAAACCCA T C YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1021497692 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93985,RMVar_hsa_circ_180978 45671 RMVar_ID_45671 Human_SNP_ID_614670811 A-to-I Human chr17 - 1352664 1352657 1352665 AAAATTGGCTGGGCGTGGTGGCGGGCTCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCCGGAGA AAAATTGGCTGGGCGTGGTGGCGGGCTCCTG________GCTACTCAGGAGGCTGAGGCCGGAGA CTGGGACTA C YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1412134172 Functional Loss DEL dbSNP153 32..39 33 - - - RMVar_hsa_circ_93985,RMVar_hsa_circ_180978 45672 RMVar_ID_45672 Human_SNP_ID_614670812 A-to-I Human chr17 - 1352658 1352658 1352658 GGCTGGGCGTGGTGGCGGGCTCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCCGGAGAATTGCT GGCTGGGCGTGGTGGCGGGCTCCTGTAGTCCCCGCTACTCAGGAGGCTGAGGCCGGAGAATTGCT T G YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs979625761 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93985,RMVar_hsa_circ_180978 45673 RMVar_ID_45673 Human_SNP_ID_614670850 A-to-I Human chr17 - 1352754 1352754 1352754 TTGGGACGCCATGGCGGGTGGATCACGCGGTCAGGAGATCGAGACCATCCTGGCTAACACGGGGA TTGGGACGCCATGGCGGGTGGATCACGCGGTCGGGAGATCGAGACCATCCTGGCTAACACGGGGA T C YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs950313210 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25248507 RMVar_hsa_circ_93985,RMVar_hsa_circ_180978 45674 RMVar_ID_45674 Human_SNP_ID_614670871 A-to-I Human chr17 - 1352800 1352800 1352800 TAAGGCTGTGCCGGGCGCGGTGGCTCATGCCTATAATCCCAGCACTTTGGGACGCCATGGCGGGT TAAGGCTGTGCCGGGCGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGACGCCATGGCGGGT T C YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1239896342 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93985,RMVar_hsa_circ_180978 45675 RMVar_ID_45675 Human_SNP_ID_614670996 A-to-I Human chr17 - 1353182 1353182 1353182 CACCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGCAAGCCACCGTGCCCGGCCTGTTTTT CACCCGCCTCGGCCTCCCAAAGTGCTGGGATTGCAGGCGCAAGCCACCGTGCCCGGCCTGTTTTT T C YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444085102 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93985,RMVar_hsa_circ_180978 45676 RMVar_ID_45676 Human_SNP_ID_614671920 A-to-I Human chr17 - 1355262 1355262 1355262 GTCCCGGCTACTCGGGAGGCTGAGGCAGGATAATGGTGTGAACCCAGGAGGCGGAGCTTGCATTT GTCCCGGCTACTCGGGAGGCTGAGGCAGGATAGTGGTGTGAACCCAGGAGGCGGAGCTTGCATTT T C YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1289707772 Functional Loss SNV dbSNP153 33..33 33 - - - 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 45677 RMVar_ID_45677 Human_SNP_ID_614671938 A-to-I Human chr17 - 1355295 1355295 1355295 CAAATCAGCCGGGTGTGGTGGCGGGCGCCTGTAGTCCCGGCTACTCGGGAGGCTGAGGCAGGATA CAAATCAGCCGGGTGTGGTGGCGGGCGCCTGTCGTCCCGGCTACTCGGGAGGCTGAGGCAGGATA T G YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs369773376 Functional Loss SNV dbSNP153 33..33 33 - - - 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 45678 RMVar_ID_45678 Human_SNP_ID_614671979 A-to-I Human chr17 - 1355380 1355380 1355380 CTGAGGCGGGCACATCACGAGGTCAGAAGATCAAGACCATCCTGGCTAACACGGTGAAACCCTGC CTGAGGCGGGCACATCACGAGGTCAGAAGATCGAGACCATCCTGGCTAACACGGTGAAACCCTGC T C YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1023258946 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9844688,Human_RBP_ID_25248544 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 45679 RMVar_ID_45679 Human_SNP_ID_614671997 A-to-I Human chr17 - 1355431 1355431 1355431 CATTAATACTTTGTTAAATATCTCAACCTTGTAATCCAGCACTTTGGGAGGCTGAGGCGGGCACA CATTAATACTTTGTTAAATATCTCAACCTTGTGATCCAGCACTTTGGGAGGCTGAGGCGGGCACA T C YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928239104 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1848645,Human_RBP_ID_3512022,Human_RBP_ID_12886106,Human_RBP_ID_23166680,Human_RBP_ID_23710888 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 45680 RMVar_ID_45680 Human_SNP_ID_614672186 A-to-I Human chr17 - 1355956 1355956 1355956 CACTGTGTTAGCCAGGATGGTCTCGATCTCCTAACCACGTGATCCGCCCGCTTCTGCCTCCCAAA CACTGTGTTAGCCAGGATGGTCTCGATCTCCTGACCACGTGATCCGCCCGCTTCTGCCTCCCAAA T C YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1248037452 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12886127 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 45681 RMVar_ID_45681 Human_SNP_ID_614673456 A-to-I Human chr17 - 1358682 1358682 1358682 GGGATTACAGGCATGTGCCACCATGCTTGGCTAATTTTTGGGGGCATTTTTAGTAGAGACGAGGT GGGATTACAGGCATGTGCCACCATGCTTGGCTGATTTTTGGGGGCATTTTTAGTAGAGACGAGGT T C YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs906584027 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6558660,Human_RBP_ID_12886208 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 45682 RMVar_ID_45682 Human_SNP_ID_614673577 A-to-I Human chr17 - 1358972 1358972 1358972 GCCACCATGCCTGGCTAATTTTTTGTATTTTTAGTAGGGATGGGGTTTCACAGTGTTGGCCAGGC GCCACCATGCCTGGCTAATTTTTTGTATTTTTGGTAGGGATGGGGTTTCACAGTGTTGGCCAGGC T C YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1428651749 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12886223 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 45683 RMVar_ID_45683 Human_SNP_ID_614674075 A-to-I Human chr17 - 1360100 1360098 1360100 AAATTAGCCGGGTGTGGTGGTGCATGCCTGCAATCCCAGTTACTCGGGAGGCTGAGACAGGAGAA AAATTAGCCGGGTGTGGTGGTGCATGCCTGCA__CCCAGTTACTCGGGAGGCTGAGACAGGAGAA GAT G YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs951795973 Functional Loss DEL dbSNP153 33..34 33 - - - 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 45684 RMVar_ID_45684 Human_SNP_ID_614674076 A-to-I Human chr17 - 1360100 1360100 1360100 AAATTAGCCGGGTGTGGTGGTGCATGCCTGCAATCCCAGTTACTCGGGAGGCTGAGACAGGAGAA AAATTAGCCGGGTGTGGTGGTGCATGCCTGCACTCCCAGTTACTCGGGAGGCTGAGACAGGAGAA T G YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs747507689 Functional Loss SNV dbSNP153 33..33 33 - - - 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 45685 RMVar_ID_45685 Human_SNP_ID_614674091 A-to-I Human chr17 - 1360141 1360141 1360141 CCTGACCAACATGGTGAAACTCTGTCTCTATTAAAAATACAAAATTAGCCGGGTGTGGTGGTGCA CCTGACCAACATGGTGAAACTCTGTCTCTATTTAAAATACAAAATTAGCCGGGTGTGGTGGTGCA T A YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1160069528 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9844709 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 45686 RMVar_ID_45686 Human_SNP_ID_614674105 A-to-I Human chr17 - 1360174 1360174 1360174 GTGGGTCACCTGAGATCAGGAGTTCGATACCAACCTGACCAACATGGTGAAACTCTGTCTCTATT GTGGGTCACCTGAGATCAGGAGTTCGATACCAGCCTGACCAACATGGTGAAACTCTGTCTCTATT T C YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs146736985 Functional Loss SNV dbSNP153 33..33 33 - - - 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 45687 RMVar_ID_45687 Human_SNP_ID_614674215 A-to-I Human chr17 - 1360544 1360544 1360544 TTGGCTAGGCTGGTCTGGAACTCCTGACCTCAAGTGATCCGCCCGCCTTCGCCTCCCAAAGTGCT TTGGCTAGGCTGGTCTGGAACTCCTGACCTCACGTGATCCGCCCGCCTTCGCCTCCCAAAGTGCT T G YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1213162378 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12886284 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 45688 RMVar_ID_45688 Human_SNP_ID_614674221 A-to-I Human chr17 - 1360579 1360579 1360579 TTTGTATTTTTAGTAGAGACGGTGTTTTCACCATTTTGGCTAGGCTGGTCTGGAACTCCTGACCT TTTGTATTTTTAGTAGAGACGGTGTTTTCACCGTTTTGGCTAGGCTGGTCTGGAACTCCTGACCT T C YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs968562377 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6558682,Human_RBP_ID_12886285,Human_RBP_ID_22946734,Human_RBP_ID_25248620 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 45689 RMVar_ID_45689 Human_SNP_ID_614674267 A-to-I Human chr17 - 1360752 1360752 1360752 TCAGTCTTTTTTTAAATTTGAGACCATGTCTCACTCTGTCTCCCAGGCTAGAGTGCAGTGGCGCC TCAGTCTTTTTTTAAATTTGAGACCATGTCTCTCTCTGTCTCCCAGGCTAGAGTGCAGTGGCGCC T A YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs796574129 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6558685,Human_RBP_ID_12886289 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 45690 RMVar_ID_45690 Human_SNP_ID_614674268 A-to-I Human chr17 - 1360752 1360752 1360752 TCAGTCTTTTTTTAAATTTGAGACCATGTCTCACTCTGTCTCCCAGGCTAGAGTGCAGTGGCGCC TCAGTCTTTTTTTAAATTTGAGACCATGTCTCGCTCTGTCTCCCAGGCTAGAGTGCAGTGGCGCC T C YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs796574129 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6558685,Human_RBP_ID_12886289 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 45691 RMVar_ID_45691 Human_SNP_ID_614677653 A-to-I Human chr17 - 1370516 1370516 1370516 TGAGGCAGGAGAATTGCTTGAACCCTGGAGGCAGAGGCTGCAGTGAGCCGAGATTGTGCCACTGC TGAGGCAGGAGAATTGCTTGAACCCTGGAGGCGGAGGCTGCAGTGAGCCGAGATTGTGCCACTGC T C YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1226963841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25248737 RMVar_hsa_circ_93985,RMVar_hsa_circ_180978,RMVar_hsa_circ_96697,RMVar_hsa_circ_180983 45692 RMVar_ID_45692 Human_SNP_ID_614677654 A-to-I Human chr17 - 1370516 1370516 1370516 TGAGGCAGGAGAATTGCTTGAACCCTGGAGGCAGAGGCTGCAGTGAGCCGAGATTGTGCCACTGC TGAGGCAGGAGAATTGCTTGAACCCTGGAGGCCGAGGCTGCAGTGAGCCGAGATTGTGCCACTGC T G YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1226963841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25248737 RMVar_hsa_circ_93985,RMVar_hsa_circ_180978,RMVar_hsa_circ_96697,RMVar_hsa_circ_180983 45693 RMVar_ID_45693 Human_SNP_ID_614677919 A-to-I Human chr17 - 1371221 1371221 1371221 AAAATTAGCTGGGCGTAATGGCGTACACCTGTAGTCCCAGCTACTCAGGAGGCTGAGGTTGGAGG AAAATTAGCTGGGCGTAATGGCGTACACCTGTCGTCCCAGCTACTCAGGAGGCTGAGGTTGGAGG T G YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs995689989 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93985,RMVar_hsa_circ_180978,RMVar_hsa_circ_96697,RMVar_hsa_circ_180983 45694 RMVar_ID_45694 Human_SNP_ID_614680135 A-to-I Human chr17 - 1378046 1378046 1378046 CCATAAAAACAATTTGAGACTTTTATTTTGAGACGGAGTCTCACCTCTGTTGCCCAGGCTGGAGT CCATAAAAACAATTTGAGACTTTTATTTTGAGGCGGAGTCTCACCTCTGTTGCCCAGGCTGGAGT T C YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1273103393 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12887055,Human_RBP_ID_23711038 RMVar_hsa_circ_93985,RMVar_hsa_circ_180978,RMVar_hsa_circ_96697,RMVar_hsa_circ_180983 45695 RMVar_ID_45695 Human_SNP_ID_614680365 A-to-I Human chr17 - 1378871 1378871 1378871 ACCTTTGCTCATTGCAACTTCCTTCGCCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCG ACCTTTGCTCATTGCAACTTCCTTCGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCG T C YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1200559844 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93985,RMVar_hsa_circ_180978,RMVar_hsa_circ_96697,RMVar_hsa_circ_180983 45696 RMVar_ID_45696 Human_SNP_ID_614681293 A-to-I Human chr17 - 1381733 1381733 1381733 TTTGTATTTTTTTGTAGAGACAGGGTTTCGCCATGTCTCCTAGGCTGGTCTTGAACTCCTGAGTT TTTGTATTTTTTTGTAGAGACAGGGTTTCGCCGTGTCTCCTAGGCTGGTCTTGAACTCCTGAGTT T C YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs933397494 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12887285,Human_RBP_ID_17566712,Human_RBP_ID_25248893 RMVar_hsa_circ_93985,RMVar_hsa_circ_180978,RMVar_hsa_circ_96697,RMVar_hsa_circ_180983 45697 RMVar_ID_45697 Human_SNP_ID_614681294 A-to-I Human chr17 - 1381733 1381733 1381733 TTTGTATTTTTTTGTAGAGACAGGGTTTCGCCATGTCTCCTAGGCTGGTCTTGAACTCCTGAGTT TTTGTATTTTTTTGTAGAGACAGGGTTTCGCCCTGTCTCCTAGGCTGGTCTTGAACTCCTGAGTT T G YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs933397494 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12887285,Human_RBP_ID_17566712,Human_RBP_ID_25248893 RMVar_hsa_circ_93985,RMVar_hsa_circ_180978,RMVar_hsa_circ_96697,RMVar_hsa_circ_180983 45698 RMVar_ID_45698 Human_SNP_ID_614681335 A-to-I Human chr17 - 1381877 1381877 1381877 ACATAGTGTCGCTCTCTCGTGCAGGCTGGAGTACAGTGGGCCAGTCTGGGCTCACTGCAGCCTTG ACATAGTGTCGCTCTCTCGTGCAGGCTGGAGTGCAGTGGGCCAGTCTGGGCTCACTGCAGCCTTG T C YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1443555152 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6558992,Human_RBP_ID_12887296,Human_RBP_ID_17566713 RMVar_hsa_circ_93985,RMVar_hsa_circ_180978,RMVar_hsa_circ_96697,RMVar_hsa_circ_180983 45699 RMVar_ID_45699 Human_SNP_ID_614681678 A-to-I Human chr17 - 1382561 1382561 1382561 GGTCAGGAGATTGAGATCATCCTGGCTAACATAGTGAAACCCCGTCTCTACTAAAGATACAAAAA GGTCAGGAGATTGAGATCATCCTGGCTAACATGGTGAAACCCCGTCTCTACTAAAGATACAAAAA T C YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1471630803 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93985,RMVar_hsa_circ_180978,RMVar_hsa_circ_96697,RMVar_hsa_circ_180983 45700 RMVar_ID_45700 Human_SNP_ID_614681940 A-to-I Human chr17 - 1383268 1383268 1383268 TCAGCTCGCGGAAACCTCGTCCTCCCAGGATCAAGCAATTCTCCTGCCTCAGCCCCCAGAGTAGC TCAGCTCGCGGAAACCTCGTCCTCCCAGGATCGAGCAATTCTCCTGCCTCAGCCCCCAGAGTAGC T C YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs951631811 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93985,RMVar_hsa_circ_180978,RMVar_hsa_circ_96697,RMVar_hsa_circ_180983 45701 RMVar_ID_45701 Human_SNP_ID_614681943 A-to-I Human chr17 - 1383274 1383274 1383274 GCGATCTCAGCTCGCGGAAACCTCGTCCTCCCAGGATCAAGCAATTCTCCTGCCTCAGCCCCCAG GCGATCTCAGCTCGCGGAAACCTCGTCCTCCCGGGATCAAGCAATTCTCCTGCCTCAGCCCCCAG T C YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1422363726 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93985,RMVar_hsa_circ_180978,RMVar_hsa_circ_96697,RMVar_hsa_circ_180983 45702 RMVar_ID_45702 Human_SNP_ID_614682035 A-to-I Human chr17 - 1383511 1383511 1383511 GGTGGCACGTGCCTGTAATCCCATCTTCTGGTAGGGGCTGAGACAGGAGAATTGCTTGAACCCGG GGTGGCACGTGCCTGTAATCCCATCTTCTGGTGGGGGCTGAGACAGGAGAATTGCTTGAACCCGG T C YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1032494307 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6559017,Human_RBP_ID_8253176,Human_RBP_ID_18513458 RMVar_hsa_circ_93985,RMVar_hsa_circ_180978,RMVar_hsa_circ_96697,RMVar_hsa_circ_180983 45703 RMVar_ID_45703 Human_SNP_ID_614682175 A-to-I Human chr17 - 1383876 1383876 1383876 TTTAAATGTGTGAAGAGATGGGGTCTTGCCATATTGCCCAGGCCGGTCTTGAACTCTTGGGCTCA TTTAAATGTGTGAAGAGATGGGGTCTTGCCATTTTGCCCAGGCCGGTCTTGAACTCTTGGGCTCA T A YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1463632830 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22475495,Human_RBP_ID_23166791,Human_RBP_ID_25248943 RMVar_hsa_circ_93985,RMVar_hsa_circ_180978,RMVar_hsa_circ_96697,RMVar_hsa_circ_180983 45704 RMVar_ID_45704 Human_SNP_ID_614682236 A-to-I Human chr17 - 1384024 1384015 1384024 TTGTTTTGTATTTTTAGTAGAAATGGGGTTTCACCATGTTGGCCAGGTTGGTCTTGAACTCTTGA TTGTTTTGTATTTTTAGTAGAAATGGGGTTTC_________GCCAGGTTGGTCTTGAACTCTTGA CCAACATGGT C YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1018751789 Functional Loss DEL dbSNP153 33..41 33 - - - RMVar_hsa_circ_93985,RMVar_hsa_circ_180978,RMVar_hsa_circ_96697,RMVar_hsa_circ_180983 45705 RMVar_ID_45705 Human_SNP_ID_614682888 A-to-I Human chr17 + 1385837 1385837 1385837 GAGCCAAAAGACTGCTATAATCCCAGCACTTTAGGAGGCCAAGGCAGGAGGACTTCTTGAGCCCA GAGCCAAAAGACTGCTATAATCCCAGCACTTTGGGAGGCCAAGGCAGGAGGACTTCTTGAGCCCA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1428170985 Functional Loss SNV dbSNP153 33..33 33 - - - 45706 RMVar_ID_45706 Human_SNP_ID_614683166 A-to-I Human chr17 - 1386830 1386830 1386830 CCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCACCTGCCACCATGCCTGGCTAATTTTTGT CCTGCCTCAGCCTCCTGAGTAGCTGGGATTACGGGCACCTGCCACCATGCCTGGCTAATTTTTGT T C YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1159435508 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93985,RMVar_hsa_circ_180978,RMVar_hsa_circ_96697,RMVar_hsa_circ_180983 45707 RMVar_ID_45707 Human_SNP_ID_614683432 A-to-I Human chr17 - 1387708 1387708 1387708 TGAGGCAGCAGAATCGCTTGAACTCGGGAGGTAGAAAGCTGCAGAATGCCGAGATTGTGGCACTG TGAGGCAGCAGAATCGCTTGAACTCGGGAGGTTGAAAGCTGCAGAATGCCGAGATTGTGGCACTG T A YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1016939291 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12887883,Human_RBP_ID_17566318,Human_RBP_ID_25249095 RMVar_hsa_circ_93985,RMVar_hsa_circ_180978,RMVar_hsa_circ_96697,RMVar_hsa_circ_180983 45708 RMVar_ID_45708 Human_SNP_ID_614683433 A-to-I Human chr17 - 1387708 1387708 1387708 TGAGGCAGCAGAATCGCTTGAACTCGGGAGGTAGAAAGCTGCAGAATGCCGAGATTGTGGCACTG TGAGGCAGCAGAATCGCTTGAACTCGGGAGGTGGAAAGCTGCAGAATGCCGAGATTGTGGCACTG T C YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1016939291 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12887883,Human_RBP_ID_17566318,Human_RBP_ID_25249095 RMVar_hsa_circ_93985,RMVar_hsa_circ_180978,RMVar_hsa_circ_96697,RMVar_hsa_circ_180983 45709 RMVar_ID_45709 Human_SNP_ID_614683466 A-to-I Human chr17 - 1387791 1387791 1387791 TGAGACCCCCCGTCTCTACTAAATATACAAAAAATTAGACGGGCGTGGTGGCGTGCGCTTGTAAT TGAGACCCCCCGTCTCTACTAAATATACAAAACATTAGACGGGCGTGGTGGCGTGCGCTTGTAAT T G YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs547882672 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12887950,Human_RBP_ID_23166826,Human_RBP_ID_25337743 RMVar_hsa_circ_93985,RMVar_hsa_circ_180978,RMVar_hsa_circ_96697,RMVar_hsa_circ_180983 45710 RMVar_ID_45710 Human_SNP_ID_614683472 A-to-I Human chr17 - 1387801 1387801 1387801 GTGAACATGGTGAGACCCCCCGTCTCTACTAAATATACAAAAAATTAGACGGGCGTGGTGGCGTG GTGAACATGGTGAGACCCCCCGTCTCTACTAAGTATACAAAAAATTAGACGGGCGTGGTGGCGTG T C YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1449709297 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12887956,Human_RBP_ID_25337743 RMVar_hsa_circ_93985,RMVar_hsa_circ_180978,RMVar_hsa_circ_96697,RMVar_hsa_circ_180983 45711 RMVar_ID_45711 Human_SNP_ID_614683484 A-to-I Human chr17 - 1387827 1387827 1387827 GAGGTCAGGAGTTCAGGATCAGGCTGGTGAACATGGTGAGACCCCCCGTCTCTACTAAATATACA GAGGTCAGGAGTTCAGGATCAGGCTGGTGAACGTGGTGAGACCCCCCGTCTCTACTAAATATACA T C YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1293680330 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12887965,Human_RBP_ID_17566319 RMVar_hsa_circ_93985,RMVar_hsa_circ_180978,RMVar_hsa_circ_96697,RMVar_hsa_circ_180983 45712 RMVar_ID_45712 Human_SNP_ID_614683777 A-to-I Human chr17 - 1388203 1388203 1388203 CAATCCTAGCACTTTGGGAGGCCGAGGAGGGCAGATCACGAGGTCAGGAGTTCGAGACAAGCCTG CAATCCTAGCACTTTGGGAGGCCGAGGAGGGCCGATCACGAGGTCAGGAGTTCGAGACAAGCCTG T G YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1318206152 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93985,RMVar_hsa_circ_180978,RMVar_hsa_circ_96697,RMVar_hsa_circ_180983 45713 RMVar_ID_45713 Human_SNP_ID_614685561 A-to-I Human chr17 - 1393632 1393632 1393632 GAGGTCAGGAGTTTGAGACCATCCTGACCAACATGGTGAAAACCAGTCTCTACTAAAAATACAAA GAGGTCAGGAGTTTGAGACCATCCTGACCAACGTGGTGAAAACCAGTCTCTACTAAAAATACAAA T C YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs894231083 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93985,RMVar_hsa_circ_180978,RMVar_hsa_circ_96697,RMVar_hsa_circ_180983 45714 RMVar_ID_45714 Human_SNP_ID_614686276 A-to-I Human chr17 - 1395446 1395446 1395446 TGGCTCACTGCAACCTCCGCCTCCCAGGTTCAAGCGGTTCTCCTGGCTCAGCCTCCCAAGTAGCT TGGCTCACTGCAACCTCCGCCTCCCAGGTTCAGGCGGTTCTCCTGGCTCAGCCTCCCAAGTAGCT T C YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs952208226 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93985,RMVar_hsa_circ_180978,RMVar_hsa_circ_96697,RMVar_hsa_circ_180983 45715 RMVar_ID_45715 Human_SNP_ID_614686277 A-to-I Human chr17 - 1395446 1395446 1395446 TGGCTCACTGCAACCTCCGCCTCCCAGGTTCAAGCGGTTCTCCTGGCTCAGCCTCCCAAGTAGCT TGGCTCACTGCAACCTCCGCCTCCCAGGTTCACGCGGTTCTCCTGGCTCAGCCTCCCAAGTAGCT T G YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs952208226 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93985,RMVar_hsa_circ_180978,RMVar_hsa_circ_96697,RMVar_hsa_circ_180983 45716 RMVar_ID_45716 Human_SNP_ID_614686733 A-to-I Human chr17 - 1396790 1396790 1396790 TGGAGAAACCCCGTCTGTAGTAAAAATACAAAATTAGCCGGGGGTGGTGGGTGCCTGTAATCCCA TGGAGAAACCCCGTCTGTAGTAAAAATACAAACTTAGCCGGGGGTGGTGGGTGCCTGTAATCCCA T G YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs538907156 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9845124,Human_RBP_ID_12888718 RMVar_hsa_circ_93985,RMVar_hsa_circ_180978,RMVar_hsa_circ_96697,RMVar_hsa_circ_180983 45717 RMVar_ID_45717 Human_SNP_ID_614695096 A-to-I Human chr17 - 1419773 1419773 1419773 CAAAAATTAGCCAGGCGTTGTGGCGTGCACCTATAGTCCCAGCTACTCGGGAGGCTGAGGCAGAT CAAAAATTAGCCAGGCGTTGTGGCGTGCACCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGAT T C lnc-CRK-1,RF00017-2012 RNACentral:URS00008B2DB2,RNACentral:URS000097430A lincRNA,SRP RNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251922711 Functional Loss SNV dbSNP153 33..33 33 - - - 45718 RMVar_ID_45718 Human_SNP_ID_614696042 A-to-I Human chr17 - 1422864 1422859 1422864 CCCCCAAACCTGTAAGTAGGTGAATTCCTAAGATAAGTGTGTATTTTCATTCCAGGTGAAAAGCA CCCCCAAACCTGTAAGTAGGTGAATTCCTAAG_____TGTGTATTTTCATTCCAGGTGAAAAGCA ACTTAT A CRK Ensembl:ENSG00000167193 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1284011715 Functional Loss DEL dbSNP153 33..37 33 - - - Human_RBP_ID_483095,Human_RBP_ID_1848860,Human_RBP_ID_3512276,Human_RBP_ID_17257893,Human_RBP_ID_17488958,Human_RBP_ID_23711231,Human_RBP_ID_26456963 RMVar_hsa_circ_180986,RMVar_hsa_circ_76030 45719 RMVar_ID_45719 Human_SNP_ID_614696044 A-to-I Human chr17 - 1422864 1422864 1422864 CCCCCAAACCTGTAAGTAGGTGAATTCCTAAGATAAGTGTGTATTTTCATTCCAGGTGAAAAGCA CCCCCAAACCTGTAAGTAGGTGAATTCCTAAGTTAAGTGTGTATTTTCATTCCAGGTGAAAAGCA T A CRK Ensembl:ENSG00000167193 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs552774877 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_483095,Human_RBP_ID_1848860,Human_RBP_ID_3512276,Human_RBP_ID_17257893,Human_RBP_ID_17488958,Human_RBP_ID_23711231,Human_RBP_ID_26456963 RMVar_hsa_circ_180986,RMVar_hsa_circ_76030 45720 RMVar_ID_45720 Human_SNP_ID_614696045 A-to-I Human chr17 - 1422864 1422864 1422864 CCCCCAAACCTGTAAGTAGGTGAATTCCTAAGATAAGTGTGTATTTTCATTCCAGGTGAAAAGCA CCCCCAAACCTGTAAGTAGGTGAATTCCTAAGGTAAGTGTGTATTTTCATTCCAGGTGAAAAGCA T C CRK Ensembl:ENSG00000167193 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs552774877 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_483095,Human_RBP_ID_1848860,Human_RBP_ID_3512276,Human_RBP_ID_17257893,Human_RBP_ID_17488958,Human_RBP_ID_23711231,Human_RBP_ID_26456963 RMVar_hsa_circ_180986,RMVar_hsa_circ_76030 45721 RMVar_ID_45721 Human_SNP_ID_614696671 A-to-I Human chr17 - 1424919 1424919 1424920 ACCTCTGCCTCCTGGGCTCAAGCAGTCCACCCACCTCAGCCTCCCGAGTAGCTGGTTCTATGAGC ACCTCTGCCTCCTGGGCTCAAGCAGTCCACCTGCCTCAGCCTCCCGAGTAGCTGGTTCTATGAGC TG CA CRK Ensembl:ENSG00000167193 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs71373935 Functional Loss MNV dbSNP153 32..33 33 - - - 45722 RMVar_ID_45722 Human_SNP_ID_614696795 A-to-I Human chr17 - 1425201 1425201 1425201 GCTGTAGTCCCAGCTACTAGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCGGGAGGCAGAGCTT GCTGTAGTCCCAGCTACTAGGGAGGCTGAGGCCGGAGAATGGCGTGAACCCGGGAGGCAGAGCTT T G CRK Ensembl:ENSG00000167193 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1446985004 Functional Loss SNV dbSNP153 33..33 33 - - - 45723 RMVar_ID_45723 Human_SNP_ID_614696877 A-to-I Human chr17 - 1425387 1425387 1425387 CTGTCTCAAAAACAAAAGATAAAAAGATGGCCAGGCGTGGTGGCTCACACCTGTAATCATAGCAC CTGTCTCAAAAACAAAAGATAAAAAGATGGCCGGGCGTGGTGGCTCACACCTGTAATCATAGCAC T C CRK Ensembl:ENSG00000167193 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs948370039 Functional Loss SNV dbSNP153 33..33 33 - - - 45724 RMVar_ID_45724 Human_SNP_ID_614697058 A-to-I Human chr17 - 1426017 1426017 1426017 CACTTGGCTTTTTAAATTTTTTTGTAGAGACAAGATCTCACTCTTTTGCCAGGGCTGCTCTCAAA CACTTGGCTTTTTAAATTTTTTTGTAGAGACAGGATCTCACTCTTTTGCCAGGGCTGCTCTCAAA T C CRK Ensembl:ENSG00000167193 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1285812683 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6559520,Human_RBP_ID_12889229 45725 RMVar_ID_45725 Human_SNP_ID_614697212 A-to-I Human chr17 - 1426501 1426501 1426501 GTCTTGAACTCCTGAGCTCAAGTGATCCTCCTACCTCGCCTCCCAAAGTGCTGGGATTAAAGACG GTCTTGAACTCCTGAGCTCAAGTGATCCTCCTGCCTCGCCTCCCAAAGTGCTGGGATTAAAGACG T C CRK Ensembl:ENSG00000167193 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs888099492 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12889253 45726 RMVar_ID_45726 Human_SNP_ID_614697257 A-to-I Human chr17 - 1426621 1426621 1426621 GACGTCGTGATTCACTCACCTCGACCTCCCAAAGTGCTGAGATTATAGGCGTGCGCCACCACGCC GACGTCGTGATTCACTCACCTCGACCTCCCAACGTGCTGAGATTATAGGCGTGCGCCACCACGCC T G CRK Ensembl:ENSG00000167193 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1194180273 Functional Loss SNV dbSNP153 33..33 33 - - - 45727 RMVar_ID_45727 Human_SNP_ID_614697706 A-to-I Human chr17 - 1427596 1427592 1427596 AGACAATATAACATTGAGGTATTTATTTATTTATTTGAGACTGAGTCTCGCTCTGTTACCCAGGC AGACAATATAACATTGAGGTATTTATTTATTT____GAGACTGAGTCTCGCTCTGTTACCCAGGC CAAAT C CRK Ensembl:ENSG00000167193 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1482143605 Functional Loss DEL dbSNP153 33..36 33 - - - 45728 RMVar_ID_45728 Human_SNP_ID_614698005 A-to-I Human chr17 - 1428396 1428394 1428396 AGTCTGAAAGAAGGGCTGGCACGGTGGCTCACACCTGTAATCCCAGCACATTGGGAGGCCGAGGT AGTCTGAAAGAAGGGCTGGCACGGTGGCTCAC__CTGTAATCCCAGCACATTGGGAGGCCGAGGT GGT G CRK Ensembl:ENSG00000167193 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1568008877 Functional Loss DEL dbSNP153 33..34 33 - - - 45729 RMVar_ID_45729 Human_SNP_ID_614698420 A-to-I Human chr17 - 1429549 1429549 1429549 CTGGGCTCAGCTGGGCAAGGTGGCCCATGCCTATAATCCCAGCACTTTGGGAGGCCGAGTTGGGC CTGGGCTCAGCTGGGCAAGGTGGCCCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGTTGGGC T C CRK Ensembl:ENSG00000167193 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1329665759 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17566717 45730 RMVar_ID_45730 Human_SNP_ID_614698513 A-to-I Human chr17 - 1429846 1429846 1429846 GCTCACTGCAGCCCCAAACTCCTGGGCTTGTGATCCCCCTACCTCAGCCTCCCAAGTAGCTGGGA GCTCACTGCAGCCCCAAACTCCTGGGCTTGTGGTCCCCCTACCTCAGCCTCCCAAGTAGCTGGGA T C CRK Ensembl:ENSG00000167193 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs967600292 Functional Loss SNV dbSNP153 33..33 33 - - - 45731 RMVar_ID_45731 Human_SNP_ID_614698654 A-to-I Human chr17 - 1430177 1430177 1430177 AGCCAGGCGTGGGGGCACACGCCTGTAATCCCAACTACGTGGGAGGCTGAGGCAGGAGAATCACT AGCCAGGCGTGGGGGCACACGCCTGTAATCCCGACTACGTGGGAGGCTGAGGCAGGAGAATCACT T C CRK Ensembl:ENSG00000167193 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs935762685 Functional Loss SNV dbSNP153 33..33 33 - - - 45732 RMVar_ID_45732 Human_SNP_ID_614698656 A-to-I Human chr17 - 1430182 1430182 1430182 AAATTAGCCAGGCGTGGGGGCACACGCCTGTAATCCCAACTACGTGGGAGGCTGAGGCAGGAGAA AAATTAGCCAGGCGTGGGGGCACACGCCTGTATTCCCAACTACGTGGGAGGCTGAGGCAGGAGAA T A CRK Ensembl:ENSG00000167193 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1054649302 Functional Loss SNV dbSNP153 33..33 33 - - - 45733 RMVar_ID_45733 Human_SNP_ID_614698657 A-to-I Human chr17 - 1430182 1430182 1430182 AAATTAGCCAGGCGTGGGGGCACACGCCTGTAATCCCAACTACGTGGGAGGCTGAGGCAGGAGAA AAATTAGCCAGGCGTGGGGGCACACGCCTGTAGTCCCAACTACGTGGGAGGCTGAGGCAGGAGAA T C CRK Ensembl:ENSG00000167193 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1054649302 Functional Loss SNV dbSNP153 33..33 33 - - - 45734 RMVar_ID_45734 Human_SNP_ID_614698666 A-to-I Human chr17 - 1430205 1430205 1430205 ACTCCATTTCTATGAAAAAGACAAAATTAGCCAGGCGTGGGGGCACACGCCTGTAATCCCAACTA ACTCCATTTCTATGAAAAAGACAAAATTAGCCGGGCGTGGGGGCACACGCCTGTAATCCCAACTA T C CRK Ensembl:ENSG00000167193 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1422916863 Functional Loss SNV dbSNP153 33..33 33 - - - 45735 RMVar_ID_45735 Human_SNP_ID_614698676 A-to-I Human chr17 - 1430251 1430248 1430252 TCACCTGAGGTCAGGAATTCGAGACCAGCCTGACTAACATTTTGAAACTCCATTTCTATGAAAAA TCACCTGAGGTCAGGAATTCGAGACCAGCCT____AACATTTTGAAACTCCATTTCTATGAAAAA TAGTC T CRK Ensembl:ENSG00000167193 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs575865432 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_12889314 45736 RMVar_ID_45736 Human_SNP_ID_614698678 A-to-I Human chr17 - 1430251 1430251 1430251 TCACCTGAGGTCAGGAATTCGAGACCAGCCTGACTAACATTTTGAAACTCCATTTCTATGAAAAA TCACCTGAGGTCAGGAATTCGAGACCAGCCTGGCTAACATTTTGAAACTCCATTTCTATGAAAAA T C CRK Ensembl:ENSG00000167193 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1377350716 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12889314 45737 RMVar_ID_45737 Human_SNP_ID_614698861 A-to-I Human chr17 - 1430521 1430521 1430521 CTCTACTAAAAAAAAAAAAAATACAAAAAATTAGCCGGACGTGGTGGCGGGCATCTGTAGTCCCA CTCTACTAAAAAAAAAAAAAATACAAAAAATTGGCCGGACGTGGTGGCGGGCATCTGTAGTCCCA T C CRK Ensembl:ENSG00000167193 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1458334409 Functional Loss SNV dbSNP153 33..33 33 - - - 45738 RMVar_ID_45738 Human_SNP_ID_614699556 A-to-I Human chr17 - 1432254 1432254 1432254 AAACTCCTGGCCTCAAGCGATCCGCCTGCCTCAGCCTCCCAAAGTGCTGGGATTATAGGCATGAG AAACTCCTGGCCTCAAGCGATCCGCCTGCCTCCGCCTCCCAAAGTGCTGGGATTATAGGCATGAG T G CRK Ensembl:ENSG00000167193 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1204420983 Functional Loss SNV dbSNP153 33..33 33 - - - 45739 RMVar_ID_45739 Human_SNP_ID_614699616 A-to-I Human chr17 - 1432388 1432388 1432388 GCCTCCTGGGTTCAAGTGATTCTCGTGCCTCAACCTCCCGGGTAGCTGGGATTACAGGCATCCAC GCCTCCTGGGTTCAAGTGATTCTCGTGCCTCAGCCTCCCGGGTAGCTGGGATTACAGGCATCCAC T C CRK Ensembl:ENSG00000167193 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1375418898 Functional Loss SNV dbSNP153 33..33 33 - - - 45740 RMVar_ID_45740 Human_SNP_ID_614699617 A-to-I Human chr17 - 1432388 1432388 1432388 GCCTCCTGGGTTCAAGTGATTCTCGTGCCTCAACCTCCCGGGTAGCTGGGATTACAGGCATCCAC GCCTCCTGGGTTCAAGTGATTCTCGTGCCTCACCCTCCCGGGTAGCTGGGATTACAGGCATCCAC T G CRK Ensembl:ENSG00000167193 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1375418898 Functional Loss SNV dbSNP153 33..33 33 - - - 45741 RMVar_ID_45741 Human_SNP_ID_614700055 A-to-I Human chr17 - 1433604 1433604 1433604 TAAGACAGGAGAATCACTTGAACCCGGGAGGCAGAGATTTCAGTGAGCTGAGATCGTGCCATAGC TAAGACAGGAGAATCACTTGAACCCGGGAGGCGGAGATTTCAGTGAGCTGAGATCGTGCCATAGC T C CRK Ensembl:ENSG00000167193 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1198843293 Functional Loss SNV dbSNP153 33..33 33 - - - 45742 RMVar_ID_45742 Human_SNP_ID_614700420 A-to-I Human chr17 - 1434700 1434692 1434701 CGGCTCACTGCAACCTCCGCCTCCCAGGTTCAAGTGATTCCCCTGCCTCAGTCTCCTGAGTAGTT CGGCTCACTGCAACCTCCGCCTCCCAGGTTC_________CCCTGCCTCAGTCTCCTGAGTAGTT GGAATCACTT G CRK Ensembl:ENSG00000167193 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1479372694 Functional Loss DEL dbSNP153 32..40 33 - - - 45743 RMVar_ID_45743 Human_SNP_ID_614700740 A-to-I Human chr17 - 1435802 1435802 1435802 AAAGCTAGTACAGACTGGGCACAGTGGCTCACACTTGTAATCCTAGTGCTCTGGGAGGCTAAGGC AAAGCTAGTACAGACTGGGCACAGTGGCTCACGCTTGTAATCCTAGTGCTCTGGGAGGCTAAGGC T C CRK Ensembl:ENSG00000167193 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1060460 Functional Loss SNV dbSNP153 33..33 33 - - - 45744 RMVar_ID_45744 Human_SNP_ID_614702287 A-to-I Human chr17 - 1440897 1440897 1440897 AAACTCATTTGGATTTTAGGTTTTTTGAGACAAGGTCTCTCTCTTTTGCCCAGGCTGGAATGCAG AAACTCATTTGGATTTTAGGTTTTTTGAGACAGGGTCTCTCTCTTTTGCCCAGGCTGGAATGCAG T C CRK Ensembl:ENSG00000167193 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1359332475 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12889804 45745 RMVar_ID_45745 Human_SNP_ID_614702288 A-to-I Human chr17 - 1440897 1440897 1440897 AAACTCATTTGGATTTTAGGTTTTTTGAGACAAGGTCTCTCTCTTTTGCCCAGGCTGGAATGCAG AAACTCATTTGGATTTTAGGTTTTTTGAGACACGGTCTCTCTCTTTTGCCCAGGCTGGAATGCAG T G CRK Ensembl:ENSG00000167193 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1359332475 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12889804 45746 RMVar_ID_45746 Human_SNP_ID_614702338 A-to-I Human chr17 - 1441064 1441064 1441064 GGGCGTGGTGATGCGTGCCTGTAGGCCCAGCTACTCAGGAGGCTGAGGTAAGAGGATGGCTTCAG GGGCGTGGTGATGCGTGCCTGTAGGCCCAGCTGCTCAGGAGGCTGAGGTAAGAGGATGGCTTCAG T C CRK Ensembl:ENSG00000167193 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs552725455 Functional Loss SNV dbSNP153 33..33 33 - - - 45747 RMVar_ID_45747 Human_SNP_ID_614703507 A-to-I Human chr17 - 1444274 1444274 1444274 AGGTCTTTAGCTGGGCGTGGTGGTGCACACCTATGGTCCCAGCTACCCAGGAGTCTGAGGCAGGA AGGTCTTTAGCTGGGCGTGGTGGTGCACACCTGTGGTCCCAGCTACCCAGGAGTCTGAGGCAGGA T C CRK Ensembl:ENSG00000167193 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs768395793 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17566323 45748 RMVar_ID_45748 Human_SNP_ID_614704960 A-to-I Human chr17 - 1448560 1448560 1448560 GGAGTGCAATGGCATATTCTCGGCTCACTGCAAGCTCTGCCTCCCAGGTTCAGGCAGTTCTCCTG GGAGTGCAATGGCATATTCTCGGCTCACTGCATGCTCTGCCTCCCAGGTTCAGGCAGTTCTCCTG T A CRK Ensembl:ENSG00000167193 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1291557370 Functional Loss SNV dbSNP153 33..33 33 - - - 45749 RMVar_ID_45749 Human_SNP_ID_614705413 A-to-I Human chr17 - 1449948 1449948 1449948 GTAATCCACCTGCCTTGACCTCCCAAAGTGTTAGGATTACAGGCGTGAGCCACCGTGCGCAGCTG GTAATCCACCTGCCTTGACCTCCCAAAGTGTTGGGATTACAGGCGTGAGCCACCGTGCGCAGCTG T C CRK Ensembl:ENSG00000167193 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417511319 Functional Loss SNV dbSNP153 33..33 33 - - - 45750 RMVar_ID_45750 Human_SNP_ID_614705422 A-to-I Human chr17 - 1449982 1449982 1449982 GTTGGCCAGGCTGGTCTCGATCTCCTGACCTCAAGTAATCCACCTGCCTTGACCTCCCAAAGTGT GTTGGCCAGGCTGGTCTCGATCTCCTGACCTCTAGTAATCCACCTGCCTTGACCTCCCAAAGTGT T A CRK Ensembl:ENSG00000167193 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs953804875 Functional Loss SNV dbSNP153 33..33 33 - - - 45751 RMVar_ID_45751 Human_SNP_ID_614705548 A-to-I Human chr17 - 1450319 1450319 1450319 GTATTTTTAGTAGAGAGGTGTTTCACCGTGTTAGCCAGGATGGTCTTGAGCTCCTGACCTCGTGA GTATTTTTAGTAGAGAGGTGTTTCACCGTGTTGGCCAGGATGGTCTTGAGCTCCTGACCTCGTGA T C CRK Ensembl:ENSG00000167193 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs966473096 Functional Loss SNV dbSNP153 33..33 33 - - - 45752 RMVar_ID_45752 Human_SNP_ID_614706047 A-to-I Human chr17 - 1451521 1451521 1451521 GAATTAAAGAATGGCAAGAAGAGGCCGGGCGCAGTGGCTCATGCCTGTAATTCCAGCACTTTGAG GAATTAAAGAATGGCAAGAAGAGGCCGGGCGCCGTGGCTCATGCCTGTAATTCCAGCACTTTGAG T G CRK Ensembl:ENSG00000167193 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1363097346 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1180118 45753 RMVar_ID_45753 Human_SNP_ID_614706077 A-to-I Human chr17 - 1451597 1451597 1451597 CCTTCTGACTCAGGCTGTGAGTAGCTGGGACTACAGGCACATACAGCCGCATCCAGCCCAGGTTT CCTTCTGACTCAGGCTGTGAGTAGCTGGGACTGCAGGCACATACAGCCGCATCCAGCCCAGGTTT T C CRK Ensembl:ENSG00000167193 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs991489046 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6560056,Human_RBP_ID_12891153 45754 RMVar_ID_45754 Human_SNP_ID_614706392 A-to-I Human chr17 - 1452703 1452703 1452703 CCACTGCAACCTCTGCCTTCTAGGTTTAATCAATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGAA CCACTGCAACCTCTGCCTTCTAGGTTTAATCAGTTCTCCTGCCTCAGCCTCCTGAGTAGCTGGAA T C CRK Ensembl:ENSG00000167193 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs539876228 Functional Loss SNV dbSNP153 33..33 33 - - - 45755 RMVar_ID_45755 Human_SNP_ID_614706405 A-to-I Human chr17 - 1452741 1452741 1452741 TTGTCTCCCACGCTGGAGCGCAATGGCGCGATATTGGCCCACTGCAACCTCTGCCTTCTAGGTTT TTGTCTCCCACGCTGGAGCGCAATGGCGCGATGTTGGCCCACTGCAACCTCTGCCTTCTAGGTTT T C CRK Ensembl:ENSG00000167193 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs979999704 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12891220,Human_RBP_ID_25249888 45756 RMVar_ID_45756 Human_SNP_ID_614706413 A-to-I Human chr17 - 1452751 1452751 1452751 GTTTTTACTCTTGTCTCCCACGCTGGAGCGCAATGGCGCGATATTGGCCCACTGCAACCTCTGCC GTTTTTACTCTTGTCTCCCACGCTGGAGCGCAGTGGCGCGATATTGGCCCACTGCAACCTCTGCC T C CRK Ensembl:ENSG00000167193 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs555571953 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12891222 45757 RMVar_ID_45757 Human_SNP_ID_614710402 A-to-I Human chr17 - 1464924 1464924 1464924 CCTCTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCCGGGAAGTGGAGGTT CCTCTAATCCCAGCTACTCGGGAGGCTGAGGCGGGAGAATCACTTGAACCCGGGAAGTGGAGGTT T C MYO1C Ensembl:ENSG00000197879 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1138626 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25249955 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 45758 RMVar_ID_45758 Human_SNP_ID_614710421 A-to-I Human chr17 - 1464985 1464985 1464985 CTACATGGAGAAACTCCGCCTCTAGTAAAAATACAAAATTAGCCGGGCATGGTGGTGCACGCCTC CTACATGGAGAAACTCCGCCTCTAGTAAAAATGCAAAATTAGCCGGGCATGGTGGTGCACGCCTC T C MYO1C Ensembl:ENSG00000197879 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1138607 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 45759 RMVar_ID_45759 Human_SNP_ID_614710423 A-to-I Human chr17 - 1464987 1464986 1464987 ACCTACATGGAGAAACTCCGCCTCTAGTAAAAATACAAAATTAGCCGGGCATGGTGGTGCACGCC ACCTACATGGAGAAACTCCGCCTCTAGTAAAA_TACAAAATTAGCCGGGCATGGTGGTGCACGCC AT A MYO1C Ensembl:ENSG00000197879 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1555518444 Functional Loss DEL 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 45760 RMVar_ID_45760 Human_SNP_ID_614710424 A-to-I Human chr17 - 1464988 1464988 1464988 GACCTACATGGAGAAACTCCGCCTCTAGTAAAAATACAAAATTAGCCGGGCATGGTGGTGCACGC GACCTACATGGAGAAACTCCGCCTCTAGTAAAGATACAAAATTAGCCGGGCATGGTGGTGCACGC T C MYO1C Ensembl:ENSG00000197879 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1138606 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 45761 RMVar_ID_45761 Human_SNP_ID_614710425 A-to-I Human chr17 - 1464989 1464989 1464989 TGACCTACATGGAGAAACTCCGCCTCTAGTAAAAATACAAAATTAGCCGGGCATGGTGGTGCACG TGACCTACATGGAGAAACTCCGCCTCTAGTAAGAATACAAAATTAGCCGGGCATGGTGGTGCACG T C MYO1C Ensembl:ENSG00000197879 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1138605 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 45762 RMVar_ID_45762 Human_SNP_ID_614710426 A-to-I Human chr17 - 1464990 1464990 1464990 CTGACCTACATGGAGAAACTCCGCCTCTAGTAAAAATACAAAATTAGCCGGGCATGGTGGTGCAC CTGACCTACATGGAGAAACTCCGCCTCTAGTAGAAATACAAAATTAGCCGGGCATGGTGGTGCAC T C MYO1C Ensembl:ENSG00000197879 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-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 45763 RMVar_ID_45763 Human_SNP_ID_614710427 A-to-I Human chr17 - 1464991 1464991 1464991 CCTGACCTACATGGAGAAACTCCGCCTCTAGTAAAAATACAAAATTAGCCGGGCATGGTGGTGCA CCTGACCTACATGGAGAAACTCCGCCTCTAGTGAAAATACAAAATTAGCCGGGCATGGTGGTGCA T C MYO1C Ensembl:ENSG00000197879 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1567509847 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 45764 RMVar_ID_45764 Human_SNP_ID_614710428 A-to-I Human chr17 - 1464994 1464994 1464994 CAACCTGACCTACATGGAGAAACTCCGCCTCTAGTAAAAATACAAAATTAGCCGGGCATGGTGGT CAACCTGACCTACATGGAGAAACTCCGCCTCTGGTAAAAATACAAAATTAGCCGGGCATGGTGGT T C MYO1C Ensembl:ENSG00000197879 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-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 45765 RMVar_ID_45765 Human_SNP_ID_614710443 A-to-I Human chr17 - 1465024 1465024 1465024 GCAGATAACCTGAGGTCAGGATTTCGAGACCAACCTGACCTACATGGAGAAACTCCGCCTCTAGT GCAGATAACCTGAGGTCAGGATTTCGAGACCAGCCTGACCTACATGGAGAAACTCCGCCTCTAGT T C MYO1C Ensembl:ENSG00000197879 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1138599 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12891406 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 45766 RMVar_ID_45766 Human_SNP_ID_614714578 A-to-I Human chr17 - 1475234 1475234 1475234 TTGTATTTTTGGTAGAGATGGGGTTTCACCATATTGACCAAGCTGGTCTCGAAGTACTGACTTTG TTGTATTTTTGGTAGAGATGGGGTTTCACCATGTTGACCAAGCTGGTCTCGAAGTACTGACTTTG T C MYO1C Ensembl:ENSG00000197879 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs536606781 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_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_108346,RMVar_hsa_circ_181020,RMVar_hsa_circ_53411,RMVar_hsa_circ_181019,RMVar_hsa_circ_181021,RMVar_hsa_circ_101152,RMVar_hsa_circ_181022,RMVar_hsa_circ_93895 45767 RMVar_ID_45767 Human_SNP_ID_614714596 A-to-I Human chr17 - 1475297 1475297 1475297 CTCCTTTGTCAGCCTCCTGAGTAGCTGGGACTACAGGCGCCCACCACCACGCCTGGCTAATTTTT CTCCTTTGTCAGCCTCCTGAGTAGCTGGGACTGCAGGCGCCCACCACCACGCCTGGCTAATTTTT T C MYO1C Ensembl:ENSG00000197879 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs796066403 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_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_108346,RMVar_hsa_circ_181020,RMVar_hsa_circ_53411,RMVar_hsa_circ_181019,RMVar_hsa_circ_181021,RMVar_hsa_circ_101152,RMVar_hsa_circ_181022,RMVar_hsa_circ_93895 45768 RMVar_ID_45768 Human_SNP_ID_614714914 A-to-I Human chr17 - 1476374 1476374 1476374 GAGGTCAGGAATTCAAGACCAGCCTGGCCAACATGGTGAAACCCTATCTCTATTAAAACTACAAA GAGGTCAGGAATTCAAGACCAGCCTGGCCAACGTGGTGAAACCCTATCTCTATTAAAACTACAAA T C MYO1C Ensembl:ENSG00000197879 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1361800664 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_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_108346,RMVar_hsa_circ_181020,RMVar_hsa_circ_53411,RMVar_hsa_circ_181019,RMVar_hsa_circ_181021,RMVar_hsa_circ_101152,RMVar_hsa_circ_181022,RMVar_hsa_circ_93895 45769 RMVar_ID_45769 Human_SNP_ID_614715096 A-to-I Human chr17 - 1476987 1476987 1476987 TAAAAATGCAAAAATTCGCTGGGTGTGGTGGCAGGTGCCTATAATCCCAGCTACTCGGGAGGCTG TAAAAATGCAAAAATTCGCTGGGTGTGGTGGCGGGTGCCTATAATCCCAGCTACTCGGGAGGCTG T C MYO1C Ensembl:ENSG00000197879 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs527930422 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_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_108346,RMVar_hsa_circ_181020,RMVar_hsa_circ_53411,RMVar_hsa_circ_181019,RMVar_hsa_circ_181021,RMVar_hsa_circ_101152,RMVar_hsa_circ_181022,RMVar_hsa_circ_93895 45770 RMVar_ID_45770 Human_SNP_ID_614729888 A-to-I Human chr17 - 1522446 1522446 1522446 ATCGCTTGAATCCAGGAGGCAGAGGTTGCAGTAAGCCAACTTTGCGCCACTGCACTCCAGCCTGG ATCGCTTGAATCCAGGAGGCAGAGGTTGCAGTGAGCCAACTTTGCGCCACTGCACTCCAGCCTGG T C PITPNA Ensembl:ENSG00000174238 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1420289814 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2197,RMVar_hsa_circ_346005,RMVar_hsa_circ_377615,RMVar_hsa_circ_122612,RMVar_hsa_circ_181041,RMVar_hsa_circ_181042 45771 RMVar_ID_45771 Human_SNP_ID_614731484 A-to-I Human chr17 - 1528010 1528010 1528010 ATTTTTAAAATTTTTTTAATTTTTGTAGAGACAGGATCTTGCTATGTTGTCCAGGCTGGTCTCAA ATTTTTAAAATTTTTTTAATTTTTGTAGAGACGGGATCTTGCTATGTTGTCCAGGCTGGTCTCAA T C PITPNA Ensembl:ENSG00000174238 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1363678622 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2197,RMVar_hsa_circ_346005,RMVar_hsa_circ_377615,RMVar_hsa_circ_122612,RMVar_hsa_circ_181041,RMVar_hsa_circ_181042 45772 RMVar_ID_45772 Human_SNP_ID_614731538 A-to-I Human chr17 - 1528203 1528203 1528203 CCAGGAGGCAGAAATGGTAGTGAGCCGAGATCATGCTGCTGCACTGTCCAGCCTTGGCGACAGAA CCAGGAGGCAGAAATGGTAGTGAGCCGAGATCGTGCTGCTGCACTGTCCAGCCTTGGCGACAGAA T C PITPNA Ensembl:ENSG00000174238 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1189288711 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2197,RMVar_hsa_circ_346005,RMVar_hsa_circ_377615,RMVar_hsa_circ_122612,RMVar_hsa_circ_181041,RMVar_hsa_circ_181042 45773 RMVar_ID_45773 Human_SNP_ID_614731565 A-to-I Human chr17 - 1528278 1528278 1528278 AAATCAGCCAGGTGTGGTGGTGTGTGCCTGTAATCCCAGCTACTTGGGAGGCTGAGACAGGAGAA AAATCAGCCAGGTGTGGTGGTGTGTGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGACAGGAGAA T C PITPNA Ensembl:ENSG00000174238 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs55982736 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2197,RMVar_hsa_circ_346005,RMVar_hsa_circ_377615,RMVar_hsa_circ_122612,RMVar_hsa_circ_181041,RMVar_hsa_circ_181042 45774 RMVar_ID_45774 Human_SNP_ID_614731594 A-to-I Human chr17 - 1528393 1528393 1528393 AAAAGCCTGTAATCCTAGCACTTTGGGAGGCTAAAGTTGGGCTGATCACCTGAGGTCAGAAGTTC AAAAGCCTGTAATCCTAGCACTTTGGGAGGCTGAAGTTGGGCTGATCACCTGAGGTCAGAAGTTC T C PITPNA Ensembl:ENSG00000174238 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1158957004 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2197,RMVar_hsa_circ_346005,RMVar_hsa_circ_377615,RMVar_hsa_circ_122612,RMVar_hsa_circ_181041,RMVar_hsa_circ_181042 45775 RMVar_ID_45775 Human_SNP_ID_614732455 A-to-I Human chr17 - 1531503 1531503 1531503 TTTTCTGAGACAGGCTCTCACTCTGTTGCCCAAGCTGGAGTGCAGTGGCACGATCTCGGCTCACT TTTTCTGAGACAGGCTCTCACTCTGTTGCCCAGGCTGGAGTGCAGTGGCACGATCTCGGCTCACT T C PITPNA Ensembl:ENSG00000174238 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1195394576 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12893616 RMVar_hsa_circ_2197,RMVar_hsa_circ_346005,RMVar_hsa_circ_377615,RMVar_hsa_circ_122612,RMVar_hsa_circ_181041,RMVar_hsa_circ_181042 45776 RMVar_ID_45776 Human_SNP_ID_614744872 A-to-I Human chr17 - 1573757 1573757 1573757 ACATTAATCGGGCGTGGTGGCGTGCGCCTGTAATCCCAACTACTCGGGAGCCTGAGGCAGGAGAA ACATTAATCGGGCGTGGTGGCGTGCGCCTGTAGTCCCAACTACTCGGGAGCCTGAGGCAGGAGAA T C SLC43A2 Ensembl:ENSG00000167703 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs566718413 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106858,RMVar_hsa_circ_181059 45777 RMVar_ID_45777 Human_SNP_ID_614748485 A-to-I Human chr17 - 1584551 1584551 1584551 CCTCGGCCTCCCAGAGTGCTGGGATTACAGGCATAAGCCACCACGCCCAGCCAAACGCTGTTTTC CCTCGGCCTCCCAGAGTGCTGGGATTACAGGCGTAAGCCACCACGCCCAGCCAAACGCTGTTTTC T C SLC43A2 Ensembl:ENSG00000167703 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1212176219 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82102,RMVar_hsa_circ_106858,RMVar_hsa_circ_181059,RMVar_hsa_circ_181060 45778 RMVar_ID_45778 Human_SNP_ID_614780800 A-to-I Human chr17 - 1684584 1684584 1684584 GGTTAGTGAATTTTTCTATCCCGCCGCTCCCCAGATTCTCCGGATATGGCCGGAGTGTTTCCTTA GGTTAGTGAATTTTTCTATCCCGCCGCTCCCCGGATTCTCCGGATATGGCCGGAGTGTTTCCTTA T C PRPF8 Ensembl:ENSG00000174231 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1325573309 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4465041,Human_RBP_ID_17885714,Human_RBP_ID_18689664,Human_RBP_ID_19080893,Human_RBP_ID_27249868 RMVar_hsa_circ_113651,RMVar_hsa_circ_181126 45779 RMVar_ID_45779 Human_SNP_ID_614787331 A-to-I Human chr17 + 1701873 1701873 1701873 TGCCGCTGCACTCTAGCCTGGGTGACAGAGCGAGACTCCATCTCAAAAAAAACAAAAAAAAAGAA TGCCGCTGCACTCTAGCCTGGGTGACAGAGCGTGACTCCATCTCAAAAAAAACAAAAAAAAAGAA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913951365 Functional Loss SNV dbSNP153 33..33 33 - - - 45780 RMVar_ID_45780 Human_SNP_ID_614787922 A-to-I Human chr17 - 1703977 1703977 1703977 CAGGTGATCCGCCCACCTTGGGCTCCCAAACTACTGGGATTATATGCGTGAGCCAACACACCCGG CAGGTGATCCGCCCACCTTGGGCTCCCAAACTGCTGGGATTATATGCGTGAGCCAACACACCCGG T C TLCD2 Ensembl:ENSG00000185561 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs984284481 Functional Loss SNV dbSNP153 33..33 33 - - - 45781 RMVar_ID_45781 Human_SNP_ID_614788047 A-to-I Human chr17 - 1704370 1704370 1704370 TTGCTGGCTGGGCATGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGTAGGAGGA TTGCTGGCTGGGCATGGTGGCTCACGCCTGTACTCCCAGCACTTTGGGAGGCCGAGGTAGGAGGA T G TLCD2 Ensembl:ENSG00000185561 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1431679449 Functional Loss SNV dbSNP153 33..33 33 - - - 45782 RMVar_ID_45782 Human_SNP_ID_614788051 A-to-I Human chr17 - 1704389 1704389 1704389 GTACTTCTAGAAGTCATGTTTGCTGGCTGGGCATGGTGGCTCACGCCTGTAATCCCAGCACTTTG GTACTTCTAGAAGTCATGTTTGCTGGCTGGGCCTGGTGGCTCACGCCTGTAATCCCAGCACTTTG T G TLCD2 Ensembl:ENSG00000185561 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs954483334 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_483688 45783 RMVar_ID_45783 Human_SNP_ID_614788140 A-to-I Human chr17 - 1704770 1704770 1704770 ACCTGGGAGGCCGAGGTTGTTATAATGAGCCGAGATAGTGCCACTGCAGTCCAGCAGGGGTGACA ACCTGGGAGGCCGAGGTTGTTATAATGAGCCGGGATAGTGCCACTGCAGTCCAGCAGGGGTGACA T C TLCD2 Ensembl:ENSG00000185561 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1412010021 Functional Loss SNV dbSNP153 33..33 33 - - - 45784 RMVar_ID_45784 Human_SNP_ID_614788165 A-to-I Human chr17 - 1704843 1704843 1704843 AAATTGGCCGGGCGTGGTGGCAGGCGCCCGTAATCCCGGCTACTGAGGAGGCTGAGGCAGGAGAA AAATTGGCCGGGCGTGGTGGCAGGCGCCCGTAGTCCCGGCTACTGAGGAGGCTGAGGCAGGAGAA T C TLCD2 Ensembl:ENSG00000185561 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs1567704157 Functional Loss SNV dbSNP153 33..33 33 - - - 45785 RMVar_ID_45785 Human_SNP_ID_614788690 A-to-I Human chr17 - 1706691 1706691 1706691 TGGCTCACTGCAATCTCTGCCTCCCAGGCTCAAGCAATTCTCCTGCCTCCCACCTCAGCCTCCCA TGGCTCACTGCAATCTCTGCCTCCCAGGCTCAGGCAATTCTCCTGCCTCCCACCTCAGCCTCCCA T C TLCD2 Ensembl:ENSG00000185561 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1439434836 Functional Loss SNV dbSNP153 33..33 33 - - - 45786 RMVar_ID_45786 Human_SNP_ID_614788805 A-to-I Human chr17 - 1707058 1707058 1707058 GGTTCAAGTGATTGTCCTGCCTTAGCCTCCCGAGTAGCTGTGACTTCAGGCATGCACCACCAAGC GGTTCAAGTGATTGTCCTGCCTTAGCCTCCCGGGTAGCTGTGACTTCAGGCATGCACCACCAAGC T C TLCD2 Ensembl:ENSG00000185561 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1472228892 Functional Loss SNV dbSNP153 33..33 33 - - - 45787 RMVar_ID_45787 Human_SNP_ID_614811099 A-to-I Human chr17 - 1774748 1774748 1774748 GCAGGAAAAGTAAAGTGGTAGCCGGGCATGGTAACTCACACCTGGAATCCCAGCATATTGGGAGG GCAGGAAAAGTAAAGTGGTAGCCGGGCATGGTGACTCACACCTGGAATCCCAGCATATTGGGAGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1261447268 Functional Loss SNV dbSNP153 33..33 33 - - - 45788 RMVar_ID_45788 Human_SNP_ID_614811125 A-to-I Human chr17 + 1774809 1774803 1774810 CTGCAGGCTATCACAGAACGTGTACAATCTAGACTCTAATCAACCAAATCAACGTCTTGCCATCG CTGCAGGCTATCACAGAACGTGTACAA_______TCTAATCAACCAAATCAACGTCTTGCCATCG ATCTAGAC A SERPINF1 Ensembl:ENSG00000132386 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388240547 Functional Loss DEL dbSNP153 28..34 33 - - - RMVar_hsa_circ_64660,RMVar_hsa_circ_98676,RMVar_hsa_circ_181146 45789 RMVar_ID_45789 Human_SNP_ID_614811743 A-to-I Human chr17 + 1776511 1776510 1776511 CCCCGGCTTTTGGGCTCTGAAGGACTAACCACATGCTTTCTCACTTGTCTCAGATTGCCCAGCTG CCCCGGCTTTTGGGCTCTGAAGGACTAACCATGTGCTTTCTCACTTGTCTCAGATTGCCCAGCTG CA TG SERPINF1 Ensembl:ENSG00000132386 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs386794462 Functional Loss MNV dbSNP153 32..33 33 - - - Human_RBP_ID_22657237 RMVar_hsa_circ_98676,RMVar_hsa_circ_181146 45790 RMVar_ID_45790 Human_SNP_ID_614811746 A-to-I Human chr17 + 1776511 1776511 1776511 CCCCGGCTTTTGGGCTCTGAAGGACTAACCACATGCTTTCTCACTTGTCTCAGATTGCCCAGCTG CCCCGGCTTTTGGGCTCTGAAGGACTAACCACGTGCTTTCTCACTTGTCTCAGATTGCCCAGCTG A G SERPINF1 Ensembl:ENSG00000132386 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2071022 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22657237 Clinvar_Rec_128 GWAS_ID_5485,GWAS_ID_5486,GWAS_ID_5487,GWAS_ID_5488,GWAS_ID_5489,GWAS_ID_5490,GWAS_ID_5491,GWAS_ID_5492,GWAS_ID_5493,GWAS_ID_5494,GWAS_ID_5495,GWAS_ID_5496,GWAS_ID_5497,GWAS_ID_5498,GWAS_ID_5499,GWAS_ID_5500,GWAS_ID_5501,GWAS_ID_5502,GWAS_ID_5503,GWAS_ID_5504,GWAS_ID_5505,GWAS_ID_5506,GWAS_ID_5507 RMVar_hsa_circ_98676,RMVar_hsa_circ_181146 45791 RMVar_ID_45791 Human_SNP_ID_614812350 A-to-I Human chr17 - 1778009 1778009 1778009 GTTGGTCAGGCTGGTCTCAAACTCCTGATCTCAGGTGATCCGCCCGCCTCGGCCTCCCAAAGTGC GTTGGTCAGGCTGGTCTCAAACTCCTGATCTCGGGTGATCCGCCCGCCTCGGCCTCCCAAAGTGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978728378 Functional Loss SNV dbSNP153 33..33 33 - - - 45792 RMVar_ID_45792 Human_SNP_ID_614813024 A-to-I Human chr17 - 1780278 1780278 1780278 GGTAGGCTGAGGCTGCAGTGAGCCAAGATCGCACTACTGCACTCCAGCCTGGGTGACAGAGTAAG GGTAGGCTGAGGCTGCAGTGAGCCAAGATCGCGCTACTGCACTCCAGCCTGGGTGACAGAGTAAG T C SMYD4 Ensembl:ENSG00000186532 Protein coding 3'UTR GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 29129909,30559470 RNA-Seq:(High) rs1238066101 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25338221 Human_miRNA_ID_291793,Human_miRNA_ID_501536,Human_miRNA_ID_508756,Human_miRNA_ID_2173884,Human_miRNA_ID_2177328,Human_miRNA_ID_2355824 RMVar_hsa_circ_96490,RMVar_hsa_circ_98361,RMVar_hsa_circ_181148,RMVar_hsa_circ_80652,RMVar_hsa_circ_181149,RMVar_hsa_circ_181147 45793 RMVar_ID_45793 Human_SNP_ID_614813159 A-to-I Human chr17 - 1780707 1780707 1780707 TGAGGCAGGAGAATGGGGTGAACCCGGGAGGAAGAGCTTGCAGTGAGCCGAGATCGCGCCACTGC TGAGGCAGGAGAATGGGGTGAACCCGGGAGGAGGAGCTTGCAGTGAGCCGAGATCGCGCCACTGC T C SMYD4 Ensembl:ENSG00000186532 Protein coding 3'UTR GSE38233;GSE100210;GSE99789 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 24183664,29129909,29796672 RNA-Seq:(High) rs1288512252 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96490,RMVar_hsa_circ_98361,RMVar_hsa_circ_181148,RMVar_hsa_circ_80652,RMVar_hsa_circ_181149,RMVar_hsa_circ_181147 45794 RMVar_ID_45794 Human_SNP_ID_614813181 A-to-I Human chr17 - 1780760 1780760 1780760 AAAATTAGTCGGGCGTGGTGGCGGACGCCTGTATTCACAGCTACTCGGGAGGTTGAGGCAGGAGA AAAATTAGTCGGGCGTGGTGGCGGACGCCTGTGTTCACAGCTACTCGGGAGGTTGAGGCAGGAGA T C SMYD4 Ensembl:ENSG00000186532 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs1037871986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25252989 RMVar_hsa_circ_96490,RMVar_hsa_circ_98361,RMVar_hsa_circ_181148,RMVar_hsa_circ_80652,RMVar_hsa_circ_181149,RMVar_hsa_circ_181147 45795 RMVar_ID_45795 Human_SNP_ID_614813316 A-to-I Human chr17 - 1781216 1781216 1781216 ATGGAACACAAGTTAAAGAGGTTTTGCTGGCCAGGTATGGTGGCTCACGCCTGTAATCCCAGCAC ATGGAACACAAGTTAAAGAGGTTTTGCTGGCCGGGTATGGTGGCTCACGCCTGTAATCCCAGCAC T C SMYD4 Ensembl:ENSG00000186532 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs958807063 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1810220 RMVar_hsa_circ_96490,RMVar_hsa_circ_98361,RMVar_hsa_circ_181148,RMVar_hsa_circ_80652,RMVar_hsa_circ_181149,RMVar_hsa_circ_181147 45796 RMVar_ID_45796 Human_SNP_ID_614816411 A-to-I Human chr17 - 1790721 1790721 1790721 CACGAGGTCAGAAGTTCGAGACTAGCCTGACTAACATGCTGAAACCTGTCTTCTACTAAAAATAC CACGAGGTCAGAAGTTCGAGACTAGCCTGACTGACATGCTGAAACCTGTCTTCTACTAAAAATAC T C SMYD4 Ensembl:ENSG00000186532 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1372827520 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96490,RMVar_hsa_circ_181149,RMVar_hsa_circ_367902,RMVar_hsa_circ_181150,RMVar_hsa_circ_65631,RMVar_hsa_circ_375622,RMVar_hsa_circ_291576,RMVar_hsa_circ_181152,RMVar_hsa_circ_181151 45797 RMVar_ID_45797 Human_SNP_ID_614818856 A-to-I Human chr17 - 1798191 1798191 1798191 AGGAGGCAGAGGTTGCAGTGAGCCATGATCGCACCGATGCACTCCAGCCTGGGTGAAACCCTGTC AGGAGGCAGAGGTTGCAGTGAGCCATGATCGCGCCGATGCACTCCAGCCTGGGTGAAACCCTGTC T C SMYD4 Ensembl:ENSG00000186532 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1012286548 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9847030,Human_RBP_ID_25253095 RMVar_hsa_circ_96490,RMVar_hsa_circ_181149,RMVar_hsa_circ_367902,RMVar_hsa_circ_181150,RMVar_hsa_circ_65631,RMVar_hsa_circ_375622,RMVar_hsa_circ_291576,RMVar_hsa_circ_181152,RMVar_hsa_circ_181151 45798 RMVar_ID_45798 Human_SNP_ID_614818992 A-to-I Human chr17 - 1798735 1798735 1798735 CCACCATGCCTGGCTAATTTTTTTGTGTTGTTAGTAGAGACGGGGTTTTGCCATGTTGGCCAGGT CCACCATGCCTGGCTAATTTTTTTGTGTTGTTCGTAGAGACGGGGTTTTGCCATGTTGGCCAGGT T G SMYD4 Ensembl:ENSG00000186532 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1003126583 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96490,RMVar_hsa_circ_181149,RMVar_hsa_circ_367902,RMVar_hsa_circ_181150,RMVar_hsa_circ_65631,RMVar_hsa_circ_375622,RMVar_hsa_circ_291576,RMVar_hsa_circ_181152,RMVar_hsa_circ_181151 45799 RMVar_ID_45799 Human_SNP_ID_614819255 A-to-I Human chr17 - 1799508 1799508 1799508 AAAATTAGCTGGGCATGGTGGTACATGCCTGTAGTCCCAGCTACTCGGGAGGCTAAGACAGGAGA AAAATTAGCTGGGCATGGTGGTACATGCCTGTGGTCCCAGCTACTCGGGAGGCTAAGACAGGAGA T C SMYD4 Ensembl:ENSG00000186532 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs936847049 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96490,RMVar_hsa_circ_181149,RMVar_hsa_circ_367902,RMVar_hsa_circ_181150,RMVar_hsa_circ_65631,RMVar_hsa_circ_375622,RMVar_hsa_circ_291576,RMVar_hsa_circ_181152,RMVar_hsa_circ_181151 45800 RMVar_ID_45800 Human_SNP_ID_614821187 A-to-I Human chr17 - 1805760 1805760 1805760 CTGCCCAGACTGGAGTGCAGTGGTATGATCTCAGCTCCCTGCAACCTCTGCTTCCTGAGTCCAAG CTGCCCAGACTGGAGTGCAGTGGTATGATCTCGGCTCCCTGCAACCTCTGCTTCCTGAGTCCAAG T C SMYD4 Ensembl:ENSG00000186532 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1224127838 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17565722 RMVar_hsa_circ_65631,RMVar_hsa_circ_181158,RMVar_hsa_circ_370629,RMVar_hsa_circ_102530,RMVar_hsa_circ_181157,RMVar_hsa_circ_341066 45801 RMVar_ID_45801 Human_SNP_ID_614829532 A-to-I Human chr17 + 1833798 1833798 1833798 ATCTCTTGAACCCGGGAGATAGAGGTTCCGGTAAGCCAAGATCGCACCATTGCACTCCAGCAACA ATCTCTTGAACCCGGGAGATAGAGGTTCCGGTTAGCCAAGATCGCACCATTGCACTCCAGCAACA A T RPA1 Ensembl:ENSG00000132383 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1476795261 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79735,RMVar_hsa_circ_85244,RMVar_hsa_circ_181159,RMVar_hsa_circ_181160 45802 RMVar_ID_45802 Human_SNP_ID_614832552 A-to-I Human chr17 + 1845041 1845041 1845041 GAACTCCTGAGATCAGGCAATCTGCCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGCGAG GAACTCCTGAGATCAGGCAATCTGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGCGAG A G RPA1 Ensembl:ENSG00000132383 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs910979421 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15338,RMVar_hsa_circ_85244,RMVar_hsa_circ_181166,RMVar_hsa_circ_105617,RMVar_hsa_circ_272593,RMVar_hsa_circ_340745,RMVar_hsa_circ_181160,RMVar_hsa_circ_359370,RMVar_hsa_circ_371333,RMVar_hsa_circ_288639,RMVar_hsa_circ_275913,RMVar_hsa_circ_121011,RMVar_hsa_circ_270346,RMVar_hsa_circ_113758,RMVar_hsa_circ_181170,RMVar_hsa_circ_79085,RMVar_hsa_circ_101836,RMVar_hsa_circ_181172,RMVar_hsa_circ_181171,RMVar_hsa_circ_181168,RMVar_hsa_circ_181169,RMVar_hsa_circ_181167,RMVar_hsa_circ_181162,RMVar_hsa_circ_181164,RMVar_hsa_circ_181165,RMVar_hsa_circ_181163,RMVar_hsa_circ_181161,RMVar_hsa_circ_90013,RMVar_hsa_circ_38016,RMVar_hsa_circ_120986,RMVar_hsa_circ_181175,RMVar_hsa_circ_268483,RMVar_hsa_circ_346349,RMVar_hsa_circ_123619,RMVar_hsa_circ_84814,RMVar_hsa_circ_181177,RMVar_hsa_circ_181178,RMVar_hsa_circ_181179,RMVar_hsa_circ_181176 45803 RMVar_ID_45803 Human_SNP_ID_614834358 A-to-I Human chr17 + 1851293 1851293 1851293 GTATGTGCGTGTGCGTGTGTGTGTGTGTGCCCACACAATCTATATGAATCAGAATCCAAAATAAG GTATGTGCGTGTGCGTGTGTGTGTGTGTGCCCGCACAATCTATATGAATCAGAATCCAAAATAAG A G RPA1 Ensembl:ENSG00000132383 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4790831 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1091675,Human_RBP_ID_23713592 RMVar_hsa_circ_15338,RMVar_hsa_circ_85244,RMVar_hsa_circ_181166,RMVar_hsa_circ_105617,RMVar_hsa_circ_272593,RMVar_hsa_circ_340745,RMVar_hsa_circ_181160,RMVar_hsa_circ_359370,RMVar_hsa_circ_371333,RMVar_hsa_circ_288639,RMVar_hsa_circ_275913,RMVar_hsa_circ_121011,RMVar_hsa_circ_270346,RMVar_hsa_circ_113758,RMVar_hsa_circ_181170,RMVar_hsa_circ_79085,RMVar_hsa_circ_101836,RMVar_hsa_circ_181172,RMVar_hsa_circ_181171,RMVar_hsa_circ_181168,RMVar_hsa_circ_181169,RMVar_hsa_circ_181167,RMVar_hsa_circ_181162,RMVar_hsa_circ_181164,RMVar_hsa_circ_181165,RMVar_hsa_circ_181163,RMVar_hsa_circ_181161,RMVar_hsa_circ_90013,RMVar_hsa_circ_38016,RMVar_hsa_circ_120986,RMVar_hsa_circ_181175,RMVar_hsa_circ_268483,RMVar_hsa_circ_346349,RMVar_hsa_circ_123619,RMVar_hsa_circ_84814,RMVar_hsa_circ_181177,RMVar_hsa_circ_181178,RMVar_hsa_circ_181179,RMVar_hsa_circ_181176 45804 RMVar_ID_45804 Human_SNP_ID_614838301 A-to-I Human chr17 + 1866121 1866121 1866121 AAAATTAGCCAGGCGTGGTGGTGTACACCTGCAGTCCTAGCCACCCGGGAGGCTGAGGTGAGAGG AAAATTAGCCAGGCGTGGTGGTGTACACCTGCTGTCCTAGCCACCCGGGAGGCTGAGGTGAGAGG A T RPA1 Ensembl:ENSG00000132383 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270856671 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15338,RMVar_hsa_circ_85244,RMVar_hsa_circ_181166,RMVar_hsa_circ_105617,RMVar_hsa_circ_272593,RMVar_hsa_circ_340745,RMVar_hsa_circ_181160,RMVar_hsa_circ_359370,RMVar_hsa_circ_371333,RMVar_hsa_circ_288639,RMVar_hsa_circ_275913,RMVar_hsa_circ_121011,RMVar_hsa_circ_113758,RMVar_hsa_circ_181170,RMVar_hsa_circ_79085,RMVar_hsa_circ_101836,RMVar_hsa_circ_181171,RMVar_hsa_circ_181168,RMVar_hsa_circ_181169,RMVar_hsa_circ_181167,RMVar_hsa_circ_181162,RMVar_hsa_circ_181164,RMVar_hsa_circ_181165,RMVar_hsa_circ_181163,RMVar_hsa_circ_181161,RMVar_hsa_circ_16814,RMVar_hsa_circ_38016,RMVar_hsa_circ_120986,RMVar_hsa_circ_268483,RMVar_hsa_circ_346349,RMVar_hsa_circ_123619,RMVar_hsa_circ_84814,RMVar_hsa_circ_316304,RMVar_hsa_circ_181177,RMVar_hsa_circ_181178,RMVar_hsa_circ_181179,RMVar_hsa_circ_181176,RMVar_hsa_circ_346821,RMVar_hsa_circ_311803,RMVar_hsa_circ_43256,RMVar_hsa_circ_181181,RMVar_hsa_circ_181182 45805 RMVar_ID_45805 Human_SNP_ID_614838396 A-to-I Human chr17 + 1866418 1866418 1866418 CTCAGTGCAACCTCTGCCTCTTGGGTTCAAGCAGTTCTCCTGTCTCAGCTTGCCTAGTAGCTGGG CTCAGTGCAACCTCTGCCTCTTGGGTTCAAGCTGTTCTCCTGTCTCAGCTTGCCTAGTAGCTGGG A T RPA1 Ensembl:ENSG00000132383 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017711087 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15338,RMVar_hsa_circ_85244,RMVar_hsa_circ_181166,RMVar_hsa_circ_105617,RMVar_hsa_circ_272593,RMVar_hsa_circ_340745,RMVar_hsa_circ_181160,RMVar_hsa_circ_359370,RMVar_hsa_circ_371333,RMVar_hsa_circ_288639,RMVar_hsa_circ_275913,RMVar_hsa_circ_121011,RMVar_hsa_circ_113758,RMVar_hsa_circ_181170,RMVar_hsa_circ_79085,RMVar_hsa_circ_101836,RMVar_hsa_circ_181171,RMVar_hsa_circ_181168,RMVar_hsa_circ_181169,RMVar_hsa_circ_181167,RMVar_hsa_circ_181162,RMVar_hsa_circ_181164,RMVar_hsa_circ_181165,RMVar_hsa_circ_181163,RMVar_hsa_circ_181161,RMVar_hsa_circ_16814,RMVar_hsa_circ_38016,RMVar_hsa_circ_120986,RMVar_hsa_circ_268483,RMVar_hsa_circ_346349,RMVar_hsa_circ_123619,RMVar_hsa_circ_84814,RMVar_hsa_circ_316304,RMVar_hsa_circ_181177,RMVar_hsa_circ_181178,RMVar_hsa_circ_181179,RMVar_hsa_circ_181176,RMVar_hsa_circ_346821,RMVar_hsa_circ_311803,RMVar_hsa_circ_43256,RMVar_hsa_circ_181181,RMVar_hsa_circ_181182 45806 RMVar_ID_45806 Human_SNP_ID_614844625 A-to-I Human chr17 + 1889617 1889617 1889617 CCCACCTCAGCCTTCCAAAGTGCTGGCATTACAAGCCTGAGCCACTGCACCCGGCCTTAAGATTT CCCACCTCAGCCTTCCAAAGTGCTGGCATTACGAGCCTGAGCCACTGCACCCGGCCTTAAGATTT A G RPA1 Ensembl:ENSG00000132383 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1567827982 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113758,RMVar_hsa_circ_79085,RMVar_hsa_circ_181162,RMVar_hsa_circ_181161,RMVar_hsa_circ_120986,RMVar_hsa_circ_268483,RMVar_hsa_circ_84814,RMVar_hsa_circ_181178,RMVar_hsa_circ_181179,RMVar_hsa_circ_48575,RMVar_hsa_circ_90489,RMVar_hsa_circ_46805,RMVar_hsa_circ_181188 45807 RMVar_ID_45807 Human_SNP_ID_614844780 A-to-I Human chr17 + 1890141 1890141 1890141 CCTGTAACCCCAGCACTTTGGAAGGCTGAGGCAGGATGATTGCTTGAGGCTGGGAGTTCGATATC CCTGTAACCCCAGCACTTTGGAAGGCTGAGGCGGGATGATTGCTTGAGGCTGGGAGTTCGATATC A G RPA1 Ensembl:ENSG00000132383 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs930958082 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23714176 RMVar_hsa_circ_113758,RMVar_hsa_circ_79085,RMVar_hsa_circ_181162,RMVar_hsa_circ_181161,RMVar_hsa_circ_120986,RMVar_hsa_circ_268483,RMVar_hsa_circ_84814,RMVar_hsa_circ_181178,RMVar_hsa_circ_181179,RMVar_hsa_circ_48575,RMVar_hsa_circ_90489,RMVar_hsa_circ_46805,RMVar_hsa_circ_181188 45808 RMVar_ID_45808 Human_SNP_ID_614889443 A-to-I Human chr17 + 2039085 2039084 2039086 CAGTCCTCTGGACTTTTTTTTTTTTTTGAGACAGAGTCTTGTTCTGTCGCCCAGGCTGGAGTGCA CAGTCCTCTGGACTTTTTTTTTTTTTTGAGAC__AGTCTTGTTCTGTCGCCCAGGCTGGAGTGCA CAG C DPH1 Ensembl:ENSG00000108963 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1180698985 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_40429 45809 RMVar_ID_45809 Human_SNP_ID_614889444 A-to-I Human chr17 + 2039085 2039085 2039085 CAGTCCTCTGGACTTTTTTTTTTTTTTGAGACAGAGTCTTGTTCTGTCGCCCAGGCTGGAGTGCA CAGTCCTCTGGACTTTTTTTTTTTTTTGAGACCGAGTCTTGTTCTGTCGCCCAGGCTGGAGTGCA A C DPH1 Ensembl:ENSG00000108963 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1267778805 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40429 45810 RMVar_ID_45810 Human_SNP_ID_614889445 A-to-I Human chr17 + 2039085 2039085 2039085 CAGTCCTCTGGACTTTTTTTTTTTTTTGAGACAGAGTCTTGTTCTGTCGCCCAGGCTGGAGTGCA CAGTCCTCTGGACTTTTTTTTTTTTTTGAGACGGAGTCTTGTTCTGTCGCCCAGGCTGGAGTGCA A G DPH1 Ensembl:ENSG00000108963 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1267778805 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40429 45811 RMVar_ID_45811 Human_SNP_ID_614889463 A-to-I Human chr17 + 2039136 2039136 2039136 CAGGCTGGAGTGCAGAGGTGCGATCTCGGCTCACTGCAGCCTCTGCCTCCCGGGTTCAAGTGATT CAGGCTGGAGTGCAGAGGTGCGATCTCGGCTCGCTGCAGCCTCTGCCTCCCGGGTTCAAGTGATT A G DPH1 Ensembl:ENSG00000108963 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1462562060 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40429 45812 RMVar_ID_45812 Human_SNP_ID_614889536 A-to-I Human chr17 + 2039322 2039322 2039322 TGACCTCGTGATCCACCCGCCTCGGCCTCCCAAAGTGTTGGGATTACAGGCATGAGCCACTGCAC TGACCTCGTGATCCACCCGCCTCGGCCTCCCACAGTGTTGGGATTACAGGCATGAGCCACTGCAC A C DPH1 Ensembl:ENSG00000108963 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1346397398 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40429 45813 RMVar_ID_45813 Human_SNP_ID_614889541 A-to-I Human chr17 + 2039341 2039341 2039341 CCTCGGCCTCCCAAAGTGTTGGGATTACAGGCATGAGCCACTGCACCTGGCAGCCCTGTGGACTT CCTCGGCCTCCCAAAGTGTTGGGATTACAGGCCTGAGCCACTGCACCTGGCAGCCCTGTGGACTT A C DPH1 Ensembl:ENSG00000108963 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1183059079 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6567542,Human_RBP_ID_12919287 RMVar_hsa_circ_40429 45814 RMVar_ID_45814 Human_SNP_ID_614889542 A-to-I Human chr17 + 2039341 2039341 2039341 CCTCGGCCTCCCAAAGTGTTGGGATTACAGGCATGAGCCACTGCACCTGGCAGCCCTGTGGACTT CCTCGGCCTCCCAAAGTGTTGGGATTACAGGCGTGAGCCACTGCACCTGGCAGCCCTGTGGACTT A G DPH1 Ensembl:ENSG00000108963 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1183059079 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6567542,Human_RBP_ID_12919287 RMVar_hsa_circ_40429 45815 RMVar_ID_45815 Human_SNP_ID_614891486 A-to-I Human chr17 - 2043585 2043585 2043585 TCCCTTCAGTTTGGGACTTAAAACTTCCACCAATAACGTGAGTATGTGCACCCATGCAGCAGCCT TCCCTTCAGTTTGGGACTTAAAACTTCCACCAGTAACGTGAGTATGTGCACCCATGCAGCAGCCT T C AC090617.5 Ensembl:ENSG00000263050 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs545774212 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1759420 45816 RMVar_ID_45816 Human_SNP_ID_614912680 A-to-I Human chr17 - 2116479 2116479 2116479 AACTCCTGACCCCACCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCATGCC AACTCCTGACCCCACCCACCTCAGCCTCCCAAGGTGCTGGGATTACAGGCGTGAGCCACCATGCC T C SMG6 Ensembl:ENSG00000070366 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1007172907 Functional Loss SNV dbSNP153 33..33 33 - - - 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_181201,RMVar_hsa_circ_119218,RMVar_hsa_circ_181203,RMVar_hsa_circ_76780,RMVar_hsa_circ_181204 45817 RMVar_ID_45817 Human_SNP_ID_614912681 A-to-I Human chr17 - 2116479 2116479 2116479 AACTCCTGACCCCACCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCATGCC AACTCCTGACCCCACCCACCTCAGCCTCCCAACGTGCTGGGATTACAGGCGTGAGCCACCATGCC T G SMG6 Ensembl:ENSG00000070366 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1007172907 Functional Loss SNV dbSNP153 33..33 33 - - - 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_181201,RMVar_hsa_circ_119218,RMVar_hsa_circ_181203,RMVar_hsa_circ_76780,RMVar_hsa_circ_181204 45818 RMVar_ID_45818 Human_SNP_ID_614913779 A-to-I Human chr17 - 2120537 2120537 2120537 ATTACAATTTTTTGTAGAGACAAGGTATTGCTATGTTGTCTATGCTGGTCTCCAGCTTCTGGGCT ATTACAATTTTTTGTAGAGACAAGGTATTGCTGTGTTGTCTATGCTGGTCTCCAGCTTCTGGGCT T C SMG6 Ensembl:ENSG00000070366 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1439288006 Functional Loss SNV dbSNP153 33..33 33 - - - 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_181201,RMVar_hsa_circ_119218,RMVar_hsa_circ_181203,RMVar_hsa_circ_76780,RMVar_hsa_circ_181204 45819 RMVar_ID_45819 Human_SNP_ID_614915667 A-to-I Human chr17 - 2127063 2127063 2127063 ACCATTACGGCTCACTGCAGCCTCGAACTCCCAAGCCCAAGGGATCCTCCCACCTCAGCTTCCTA ACCATTACGGCTCACTGCAGCCTCGAACTCCCTAGCCCAAGGGATCCTCCCACCTCAGCTTCCTA T A SMG6 Ensembl:ENSG00000070366 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1395786489 Functional Loss SNV dbSNP153 33..33 33 - - - 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_181201,RMVar_hsa_circ_119218,RMVar_hsa_circ_181203,RMVar_hsa_circ_76780,RMVar_hsa_circ_181204 45820 RMVar_ID_45820 Human_SNP_ID_614915668 A-to-I Human chr17 - 2127063 2127063 2127063 ACCATTACGGCTCACTGCAGCCTCGAACTCCCAAGCCCAAGGGATCCTCCCACCTCAGCTTCCTA ACCATTACGGCTCACTGCAGCCTCGAACTCCCGAGCCCAAGGGATCCTCCCACCTCAGCTTCCTA T C SMG6 Ensembl:ENSG00000070366 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1395786489 Functional Loss SNV dbSNP153 33..33 33 - - - 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_181201,RMVar_hsa_circ_119218,RMVar_hsa_circ_181203,RMVar_hsa_circ_76780,RMVar_hsa_circ_181204 45821 RMVar_ID_45821 Human_SNP_ID_614915827 A-to-I Human chr17 + 2127511 2127511 2127511 CCCTGCTAAATATTTAATATTATCAAGCTTGTATGACTCAAGCATGGTTTTGGGGCCAGCATCCT CCCTGCTAAATATTTAATATTATCAAGCTTGTGTGACTCAAGCATGGTTTTGGGGCCAGCATCCT A G RF00017-156 RNACentral:URS000091874B SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879109171 Functional Loss SNV dbSNP153 33..33 33 - - - 45822 RMVar_ID_45822 Human_SNP_ID_614915854 A-to-I Human chr17 - 2127601 2127601 2127601 GGAAGCTGCTGGAATTGAGAACAGAAATAGTGACATTGCATGCCCAGCAAGATTGGGCCGTCACC GGAAGCTGCTGGAATTGAGAACAGAAATAGTGGCATTGCATGCCCAGCAAGATTGGGCCGTCACC T C SMG6,MCUR1P1 Ensembl:ENSG00000070366,Ensembl:ENSG00000262402 Protein coding,Pseudogene intron,exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs879059900 Functional Loss SNV dbSNP153 33..33 33 - - - 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_181201,RMVar_hsa_circ_119218,RMVar_hsa_circ_181203,RMVar_hsa_circ_76780,RMVar_hsa_circ_181204 45823 RMVar_ID_45823 Human_SNP_ID_614915861 A-to-I Human chr17 + 2127638 2127638 2127638 ATTTCTGTTCTCAATTCCAGCAGCTTCCTTTCATTCAACGAATACAATTCTTTTACTCTGCTCTT ATTTCTGTTCTCAATTCCAGCAGCTTCCTTTCGTTCAACGAATACAATTCTTTTACTCTGCTCTT A G RF00017-156 RNACentral:URS000091874B SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1396758457 Functional Loss SNV dbSNP153 33..33 33 - - - 45824 RMVar_ID_45824 Human_SNP_ID_614915877 A-to-I Human chr17 + 2127692 2127692 2127692 ACTCTGCTCTTTTCTAGGTTGAAGTCTAATTTAGTATCTGTTCGGACTTTAATCACTTCATCCAT ACTCTGCTCTTTTCTAGGTTGAAGTCTAATTTGGTATCTGTTCGGACTTTAATCACTTCATCCAT A G RF00017-156 RNACentral:URS000091874B SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1274834098 Functional Loss SNV dbSNP153 33..33 33 - - - 45825 RMVar_ID_45825 Human_SNP_ID_614915888 A-to-I Human chr17 + 2127710 2127710 2127710 TTGAAGTCTAATTTAGTATCTGTTCGGACTTTAATCACTTCATCCATTACTTGTTTTAACTGATG TTGAAGTCTAATTTAGTATCTGTTCGGACTTTGATCACTTCATCCATTACTTGTTTTAACTGATG A G RF00017-156 RNACentral:URS000091874B SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs533694208 Functional Loss SNV dbSNP153 33..33 33 - - - 45826 RMVar_ID_45826 Human_SNP_ID_614917590 A-to-I Human chr17 - 2133689 2133689 2133689 AGAAATGTATCCAGCTATTAGCCACATGTGTTAGCACGTACCTGTAATCCTAGCTACTCTAGAGG AGAAATGTATCCAGCTATTAGCCACATGTGTTGGCACGTACCTGTAATCCTAGCTACTCTAGAGG T C SMG6 Ensembl:ENSG00000070366 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1234959409 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8446525 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_181201,RMVar_hsa_circ_119218,RMVar_hsa_circ_181203,RMVar_hsa_circ_76780,RMVar_hsa_circ_181204 45827 RMVar_ID_45827 Human_SNP_ID_614919193 A-to-I Human chr17 - 2139542 2139542 2139542 TGGCGCACGCCTGTGATCCCAGCTCCTTGGGAAGTTGAGGCTGGAGAATCGCTTGATGCCGGGAG TGGCGCACGCCTGTGATCCCAGCTCCTTGGGAGGTTGAGGCTGGAGAATCGCTTGATGCCGGGAG T C SMG6 Ensembl:ENSG00000070366 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1418524891 Functional Loss SNV dbSNP153 33..33 33 - - - 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_181201,RMVar_hsa_circ_119218,RMVar_hsa_circ_181203,RMVar_hsa_circ_76780,RMVar_hsa_circ_181204 45828 RMVar_ID_45828 Human_SNP_ID_614924798 A-to-I Human chr17 - 2160682 2160682 2160682 GGGACTATAGGCGCACGCCATCACACCTGGCTAATTTTTAAATTTTTTGTGGAAACGGGGTCCCA GGGACTATAGGCGCACGCCATCACACCTGGCTTATTTTTAAATTTTTTGTGGAAACGGGGTCCCA T A SMG6 Ensembl:ENSG00000070366 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1473574074 Functional Loss SNV dbSNP153 33..33 33 - - - 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_181201,RMVar_hsa_circ_119218,RMVar_hsa_circ_181203,RMVar_hsa_circ_76780,RMVar_hsa_circ_181204 45829 RMVar_ID_45829 Human_SNP_ID_614926143 A-to-I Human chr17 - 2165699 2165699 2165699 CAAGGCCTCCCTGTGTTGCCCAGGATGGTCTCAAACTCCTGAGCTCAAGTGATCCTCCCGCCTTG CAAGGCCTCCCTGTGTTGCCCAGGATGGTCTCGAACTCCTGAGCTCAAGTGATCCTCCCGCCTTG T C SMG6 Ensembl:ENSG00000070366 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs930125995 Functional Loss SNV dbSNP153 33..33 33 - - - 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_181201,RMVar_hsa_circ_119218,RMVar_hsa_circ_181203,RMVar_hsa_circ_76780,RMVar_hsa_circ_96845,RMVar_hsa_circ_181204,RMVar_hsa_circ_181205 45830 RMVar_ID_45830 Human_SNP_ID_614939507 A-to-I Human chr17 - 2217846 2217846 2217846 GCCACCACACCCGGCTGATTTTTTTTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGA GCCACCACACCCGGCTGATTTTTTTTATTTTTGGTAGAGACGGGGTTTCACCATGTTGGCCAGGA T C SMG6 Ensembl:ENSG00000070366 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285717883 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90111,RMVar_hsa_circ_119061,RMVar_hsa_circ_181197,RMVar_hsa_circ_181198,RMVar_hsa_circ_98730,RMVar_hsa_circ_181201,RMVar_hsa_circ_316320,RMVar_hsa_circ_324625,RMVar_hsa_circ_99574,RMVar_hsa_circ_181208,RMVar_hsa_circ_268169,RMVar_hsa_circ_319900,RMVar_hsa_circ_14269 45831 RMVar_ID_45831 Human_SNP_ID_614946184 A-to-I Human chr17 - 2242323 2242323 2242323 TATCTTCAGTAGAGATGGGGTTTTACTACGTTAGCCAGGATGGTCTCGATCTCCTGACCTCGTGG TATCTTCAGTAGAGATGGGGTTTTACTACGTTTGCCAGGATGGTCTCGATCTCCTGACCTCGTGG T A SMG6 Ensembl:ENSG00000070366 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1449729115 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90111,RMVar_hsa_circ_119061,RMVar_hsa_circ_181197,RMVar_hsa_circ_181198,RMVar_hsa_circ_98730,RMVar_hsa_circ_181201,RMVar_hsa_circ_324625,RMVar_hsa_circ_99574,RMVar_hsa_circ_181208,RMVar_hsa_circ_181211,RMVar_hsa_circ_14921,RMVar_hsa_circ_14269,RMVar_hsa_circ_344709,RMVar_hsa_circ_285372,RMVar_hsa_circ_181213,RMVar_hsa_circ_181212 45832 RMVar_ID_45832 Human_SNP_ID_614946185 A-to-I Human chr17 - 2242323 2242323 2242323 TATCTTCAGTAGAGATGGGGTTTTACTACGTTAGCCAGGATGGTCTCGATCTCCTGACCTCGTGG TATCTTCAGTAGAGATGGGGTTTTACTACGTTGGCCAGGATGGTCTCGATCTCCTGACCTCGTGG T C SMG6 Ensembl:ENSG00000070366 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1449729115 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90111,RMVar_hsa_circ_119061,RMVar_hsa_circ_181197,RMVar_hsa_circ_181198,RMVar_hsa_circ_98730,RMVar_hsa_circ_181201,RMVar_hsa_circ_324625,RMVar_hsa_circ_99574,RMVar_hsa_circ_181208,RMVar_hsa_circ_181211,RMVar_hsa_circ_14921,RMVar_hsa_circ_14269,RMVar_hsa_circ_344709,RMVar_hsa_circ_285372,RMVar_hsa_circ_181213,RMVar_hsa_circ_181212 45833 RMVar_ID_45833 Human_SNP_ID_614955329 A-to-I Human chr17 - 2275256 2275256 2275256 CACCATGCCCAGCTGATTTTTGTATTGTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGG CACCATGCCCAGCTGATTTTTGTATTGTTAGTGGAGATGGGGTTTCACCATGTTGGCCAGGCTGG T C SMG6 Ensembl:ENSG00000070366 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs771231882 Functional Loss SNV dbSNP153 33..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 45834 RMVar_ID_45834 Human_SNP_ID_614956204 A-to-I Human chr17 - 2277923 2277923 2277923 CTGCCTTAGTCTTCTGAGTAGCTGGGACTGCAAGCATGCGCCACCATGCCTGGCTAATTTTTTAA CTGCCTTAGTCTTCTGAGTAGCTGGGACTGCATGCATGCGCCACCATGCCTGGCTAATTTTTTAA T A SMG6 Ensembl:ENSG00000070366 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs764626106 Functional Loss SNV dbSNP153 33..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 45835 RMVar_ID_45835 Human_SNP_ID_614962801 A-to-I Human chr17 - 2300054 2300054 2300054 GGGGAGGGGGTGAGGGAAACCCACGACGACCCAGCCCGCGGGAGGCCGGGCTCCGCAAAGCGCTA GGGGAGGGGGTGAGGGAAACCCACGACGACCCGGCCCGCGGGAGGCCGGGCTCCGCAAAGCGCTA T C SMG6 Ensembl:ENSG00000070366 Protein coding CDS GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs216194 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - Human_RBP_ID_235684,Human_RBP_ID_764414,Human_RBP_ID_819412,Human_RBP_ID_903101,Human_RBP_ID_5525197,Human_RBP_ID_9422164,Human_RBP_ID_25257790 GWAS_ID_5508 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 45836 RMVar_ID_45836 Human_SNP_ID_614964492 A-to-I Human chr17 + 2304657 2304657 2304657 GGGACCTGTAATCCCGGCGACTCGGAACGCTGAGACGGGCGGATCGCTTGAACCCGGGAGGCGGA GGGACCTGTAATCCCGGCGACTCGGAACGCTGGGACGGGCGGATCGCTTGAACCCGGGAGGCGGA A G SRR Ensembl:ENSG00000167720 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1431641382 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12929248 45837 RMVar_ID_45837 Human_SNP_ID_614964959 A-to-I Human chr17 + 2306632 2306632 2306632 CCAGCTACTTGGGAGACTGAGGCAGGAGAATCACTTGAACCAAGGAGGTAGAGGCTGCAGTGAGC CCAGCTACTTGGGAGACTGAGGCAGGAGAATCTCTTGAACCAAGGAGGTAGAGGCTGCAGTGAGC A T SRR Ensembl:ENSG00000167720 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1216742367 Functional Loss SNV dbSNP153 33..33 33 - - - 45838 RMVar_ID_45838 Human_SNP_ID_614965648 A-to-I Human chr17 + 2309152 2309152 2309152 AAATAATAATAATAATAATAATTTGTAGAGGCAGGGTTTCCCTGTGTTGCCCAGGCTGGTCTCAA AAATAATAATAATAATAATAATTTGTAGAGGCTGGGTTTCCCTGTGTTGCCCAGGCTGGTCTCAA A T SRR Ensembl:ENSG00000167720 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs993770572 Functional Loss SNV dbSNP153 33..33 33 - - - 45839 RMVar_ID_45839 Human_SNP_ID_614966120 A-to-I Human chr17 - 2311080 2311080 2311080 GTTCAGGAGTTTGAGACCAGACTGACTAACATAGTAAAATCCCGTCTCCATTAAAAAAACAAAAA GTTCAGGAGTTTGAGACCAGACTGACTAACATCGTAAAATCCCGTCTCCATTAAAAAAACAAAAA T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1463692635 Functional Loss SNV dbSNP153 33..33 33 - - - 45840 RMVar_ID_45840 Human_SNP_ID_614967895 A-to-I Human chr17 - 2317664 2317664 2317664 AGTCTCCGTTATCCCGGCTGGAGTGCAGTGCCACGATCTCGGCTTACTGCAACGTCCGCCTCCCC AGTCTCCGTTATCCCGGCTGGAGTGCAGTGCCGCGATCTCGGCTTACTGCAACGTCCGCCTCCCC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1430968428 Functional Loss SNV dbSNP153 33..33 33 - - - 45841 RMVar_ID_45841 Human_SNP_ID_614967912 A-to-I Human chr17 - 2317711 2317704 2317711 TCTTAAATATCTCATGTGCATCTTTATTTTTTATTTTTTTGAGATGGAGTCTCCGTTATCCCGGC TCTTAAATATCTCATGTGCATCTTTATTTTTT_______TGAGATGGAGTCTCCGTTATCCCGGC AAAAAAAT A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1309380200 Functional Loss DEL dbSNP153 33..39 33 - - - Human_RBP_ID_6570298 45842 RMVar_ID_45842 Human_SNP_ID_614968597 A-to-I Human chr17 - 2319929 2319929 2319929 CTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAAGAGAATCGCTGGAACCCAGGAGGCGGGGCTTG CTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTGGAACCCAGGAGGCGGGGCTTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs911278728 Functional Loss SNV dbSNP153 33..33 33 - - - 45843 RMVar_ID_45843 Human_SNP_ID_614968675 A-to-I Human chr17 - 2320113 2320113 2320113 GATTTAGACTTGAAAAGAGACAAGTTCTGGCCAGGCGTGGTGGCTCACGCCTGTAATCCCAGCAC GATTTAGACTTGAAAAGAGACAAGTTCTGGCCGGGCGTGGTGGCTCACGCCTGTAATCCCAGCAC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs371372028 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13224400 45844 RMVar_ID_45844 Human_SNP_ID_614969200 A-to-I Human chr17 - 2321854 2321854 2321854 AGAATCGCTTGAACCCGGGAGGTGGAGGCTGCAGTGGGCCAGGATCGTGCCACTGCACTCCAGCC AGAATCGCTTGAACCCGGGAGGTGGAGGCTGCGGTGGGCCAGGATCGTGCCACTGCACTCCAGCC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs575941289 Functional Loss SNV dbSNP153 33..33 33 - - - 45845 RMVar_ID_45845 Human_SNP_ID_614969293 A-to-I Human chr17 - 2322208 2322206 2322208 AAGAAGAGAGTTGGCTGGGTGCGGTGGCTCACACCTGTAATCCTAGCACTTTGGGAGGCCAAAGT AAGAAGAGAGTTGGCTGGGTGCGGTGGCTCAC__CTGTAATCCTAGCACTTTGGGAGGCCAAAGT GGT G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1391940505 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_12929506 45846 RMVar_ID_45846 Human_SNP_ID_614970743 A-to-I Human chr17 + 2327158 2327158 2327158 TTCGTAGAGGCCGGGCATGTTGGCTCATCCCTATAAATCCCAGCACTTTGGGAGGCCAAGGCACG TTCGTAGAGGCCGGGCATGTTGGCTCATCCCTGTAAATCCCAGCACTTTGGGAGGCCAAGGCACG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs561189304 Functional Loss SNV dbSNP153 33..33 33 - - - 45847 RMVar_ID_45847 Human_SNP_ID_614970788 A-to-I Human chr17 + 2327358 2327358 2327358 AGAATCACTTGAACCTGGGACGGGGAGGCTGCAATGAGCTGAGATCATGTTACTGCACTCCAGCC AGAATCACTTGAACCTGGGACGGGGAGGCTGCGATGAGCTGAGATCATGTTACTGCACTCCAGCC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1447429733 Functional Loss SNV dbSNP153 33..33 33 - - - 45848 RMVar_ID_45848 Human_SNP_ID_614971088 A-to-I Human chr17 - 2328502 2328502 2328502 TCACTGCAACCTCCGCCTCCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGAGTAGT TCACTGCAACCTCCGCCTCCCGGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCCGAGTAGAGTAGT T C TSR1 Ensembl:ENSG00000167721 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1168926710 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25862 45849 RMVar_ID_45849 Human_SNP_ID_614987650 A-to-I Human chr17 - 2380139 2380139 2380139 TCAGGTGGCCAAAGGCAGTGGCAGTGCTGCTGAAGTGGGCTGCTCCCACCCAGGGCCCACATCTT TCAGGTGGCCAAAGGCAGTGGCAGTGCTGCTGGAGTGGGCTGCTCCCACCCAGGGCCCACATCTT T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs889969685 Functional Loss SNV dbSNP153 33..33 33 - - - 45850 RMVar_ID_45850 Human_SNP_ID_614998442 A-to-I Human chr17 - 2409520 2409520 2409520 GAAATACCATCTCTACAAAAAATAAAAAAATTAGTCGGGTGTGGTGGTGCACGCCTGTAGTCCCA GAAATACCATCTCTACAAAAAATAAAAAAATTTGTCGGGTGTGGTGGTGCACGCCTGTAGTCCCA T A METTL16 Ensembl:ENSG00000127804 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs574107476 Functional Loss SNV dbSNP153 33..33 33 - - - 45851 RMVar_ID_45851 Human_SNP_ID_614999185 A-to-I Human chr17 - 2411697 2411697 2411697 TGTAAACCAGCTGGGCATGGTGGCGCAAGCCTATAATCCTAGCACCTTTGGGAGGCTGAGGTTGG TGTAAACCAGCTGGGCATGGTGGCGCAAGCCTGTAATCCTAGCACCTTTGGGAGGCTGAGGTTGG T C METTL16 Ensembl:ENSG00000127804 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941357891 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25258048 45852 RMVar_ID_45852 Human_SNP_ID_615000774 A-to-I Human chr17 - 2417160 2417160 2417160 ACTCGGGAGGCTGAGGCAGGAGACTCGCTTGAACCTGGGAGGTGGAGGTTGCAGTGAGCCGAGAA ACTCGGGAGGCTGAGGCAGGAGACTCGCTTGATCCTGGGAGGTGGAGGTTGCAGTGAGCCGAGAA T A METTL16 Ensembl:ENSG00000127804 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1190598377 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80864,RMVar_hsa_circ_181248,RMVar_hsa_circ_79299,RMVar_hsa_circ_181247 45853 RMVar_ID_45853 Human_SNP_ID_615000799 A-to-I Human chr17 - 2417220 2417220 2417220 GTCTCTACTCAAAATACAAAAATTAGCCGGGCATGATAGCACGTGCCTGTAATCCCAGCTACTCG GTCTCTACTCAAAATACAAAAATTAGCCGGGCGTGATAGCACGTGCCTGTAATCCCAGCTACTCG T C METTL16 Ensembl:ENSG00000127804 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs547543528 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80864,RMVar_hsa_circ_181248,RMVar_hsa_circ_79299,RMVar_hsa_circ_181247 45854 RMVar_ID_45854 Human_SNP_ID_615000803 A-to-I Human chr17 - 2417228 2417228 2417228 GAAACCCCGTCTCTACTCAAAATACAAAAATTAGCCGGGCATGATAGCACGTGCCTGTAATCCCA GAAACCCCGTCTCTACTCAAAATACAAAAATTCGCCGGGCATGATAGCACGTGCCTGTAATCCCA T G METTL16 Ensembl:ENSG00000127804 Protein coding intron GSE47997;GSE38233;GSE38233 K562 cells&HepG2 cells;cultured B-cells;cultured B-cells - 23474544,24183664,24183664 RNA-Seq:(High) rs1435341531 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80864,RMVar_hsa_circ_181248,RMVar_hsa_circ_79299,RMVar_hsa_circ_181247 45855 RMVar_ID_45855 Human_SNP_ID_615001102 A-to-I Human chr17 - 2418318 2418318 2418318 CCAAAGTGCTGGGATTACAGCCGTGAGCCACTACTCCCAGCCTCTGACCAGTGTTCTTAACCTGG CCAAAGTGCTGGGATTACAGCCGTGAGCCACTTCTCCCAGCCTCTGACCAGTGTTCTTAACCTGG T A METTL16 Ensembl:ENSG00000127804 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,31158229,31158229,32596459 RNA-Seq:(High) rs576940492 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80864,RMVar_hsa_circ_181248,RMVar_hsa_circ_79299,RMVar_hsa_circ_181247 45856 RMVar_ID_45856 Human_SNP_ID_615001103 A-to-I Human chr17 - 2418318 2418318 2418318 CCAAAGTGCTGGGATTACAGCCGTGAGCCACTACTCCCAGCCTCTGACCAGTGTTCTTAACCTGG CCAAAGTGCTGGGATTACAGCCGTGAGCCACTCCTCCCAGCCTCTGACCAGTGTTCTTAACCTGG T G METTL16 Ensembl:ENSG00000127804 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,31158229,31158229,32596459 RNA-Seq:(High) rs576940492 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80864,RMVar_hsa_circ_181248,RMVar_hsa_circ_79299,RMVar_hsa_circ_181247 45857 RMVar_ID_45857 Human_SNP_ID_615001124 A-to-I Human chr17 - 2418393 2418393 2418393 AGAGATGGGATTTCACCATGTTGGCCAGGCTAATCTCGAACTCATGATCTCGGGTGATCCGCCCA AGAGATGGGATTTCACCATGTTGGCCAGGCTAGTCTCGAACTCATGATCTCGGGTGATCCGCCCA T C METTL16 Ensembl:ENSG00000127804 Protein coding intron GSE38233;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,32596459 RNA-Seq:(High) rs1008610764 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80864,RMVar_hsa_circ_181248,RMVar_hsa_circ_79299,RMVar_hsa_circ_181247 45858 RMVar_ID_45858 Human_SNP_ID_615001125 A-to-I Human chr17 - 2418394 2418394 2418394 TAGAGATGGGATTTCACCATGTTGGCCAGGCTAATCTCGAACTCATGATCTCGGGTGATCCGCCC TAGAGATGGGATTTCACCATGTTGGCCAGGCTGATCTCGAACTCATGATCTCGGGTGATCCGCCC T C METTL16 Ensembl:ENSG00000127804 Protein coding intron GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,29796672,31158229,31158229,32596459,32596459 RNA-Seq:(High) rs1019628567 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80864,RMVar_hsa_circ_181248,RMVar_hsa_circ_79299,RMVar_hsa_circ_181247 45859 RMVar_ID_45859 Human_SNP_ID_615001174 A-to-I Human chr17 - 2418538 2418538 2418538 TTGTCTAGGCTGGAGTGCCGTGGTGCGATCTTAGCTCACTGCAACCCCCGCCTCCCGGGTTCAAG TTGTCTAGGCTGGAGTGCCGTGGTGCGATCTTGGCTCACTGCAACCCCCGCCTCCCGGGTTCAAG T C METTL16 Ensembl:ENSG00000127804 Protein coding intron GSE38233;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,32596459 RNA-Seq:(High) rs1382317160 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23308074,Human_RBP_ID_26957119 RMVar_hsa_circ_80864,RMVar_hsa_circ_181248,RMVar_hsa_circ_79299,RMVar_hsa_circ_181247 45860 RMVar_ID_45860 Human_SNP_ID_615003538 A-to-I Human chr17 - 2426642 2426642 2426642 TCACTGCAACCTCCGACTCCCTGGTTCGAGCAATTCTCCTGCCTCAGCCTGCCGAGTAGCTGGGA TCACTGCAACCTCCGACTCCCTGGTTCGAGCAGTTCTCCTGCCTCAGCCTGCCGAGTAGCTGGGA T C METTL16 Ensembl:ENSG00000127804 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs544149766 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80864,RMVar_hsa_circ_181248,RMVar_hsa_circ_79299,RMVar_hsa_circ_181247 45861 RMVar_ID_45861 Human_SNP_ID_615005372 A-to-I Human chr17 - 2432342 2432342 2432342 GTTGGTCTTGAACTCCTGGGCTCAAGTGATCCACCTTCCTCGGCCTCCCACAGTGCTGGGATTAC GTTGGTCTTGAACTCCTGGGCTCAAGTGATCCGCCTTCCTCGGCCTCCCACAGTGCTGGGATTAC T C METTL16 Ensembl:ENSG00000127804 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1019073093 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80864,RMVar_hsa_circ_181248,RMVar_hsa_circ_79299,RMVar_hsa_circ_181247 45862 RMVar_ID_45862 Human_SNP_ID_615013772 A-to-I Human chr17 - 2463727 2463727 2463727 GGCTGGGCGTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGCAGATCAGA GGCTGGGCGTGGTGGCTCACACCTGTAATCCCGGCACTTTGGGAGGCCGAGGTGGGCAGATCAGA T C METTL16 Ensembl:ENSG00000127804 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285460389 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63994,RMVar_hsa_circ_74724,RMVar_hsa_circ_80864,RMVar_hsa_circ_181248,RMVar_hsa_circ_79299,RMVar_hsa_circ_181247,RMVar_hsa_circ_181250,RMVar_hsa_circ_47384,RMVar_hsa_circ_286255,RMVar_hsa_circ_316302,RMVar_hsa_circ_280298,RMVar_hsa_circ_181251,RMVar_hsa_circ_346020,RMVar_hsa_circ_181249,RMVar_hsa_circ_265760,RMVar_hsa_circ_181252 45863 RMVar_ID_45863 Human_SNP_ID_615015295 A-to-I Human chr17 - 2469161 2469161 2469161 CAATCTGCTGCTCACTGCAACCTCTGTCTCCCAGGTTCAAGTGATTCTCCTGCCTCAGCCTCCTG CAATCTGCTGCTCACTGCAACCTCTGTCTCCCGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCTG T C METTL16 Ensembl:ENSG00000127804 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1252930652 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80864,RMVar_hsa_circ_181248,RMVar_hsa_circ_79299,RMVar_hsa_circ_181247,RMVar_hsa_circ_47384,RMVar_hsa_circ_280298,RMVar_hsa_circ_181251,RMVar_hsa_circ_346020,RMVar_hsa_circ_181255,RMVar_hsa_circ_277762,RMVar_hsa_circ_341741,RMVar_hsa_circ_287833,RMVar_hsa_circ_181256,RMVar_hsa_circ_181257,RMVar_hsa_circ_290901,RMVar_hsa_circ_354809 45864 RMVar_ID_45864 Human_SNP_ID_615015917 A-to-I Human chr17 - 2471741 2471741 2471741 GCTCTGTCGCCAGGCTGGAGTGCAGTGGCGCAATCTCGGCTCATTGCAAGCTCCGCCTGCTGGGT GCTCTGTCGCCAGGCTGGAGTGCAGTGGCGCAGTCTCGGCTCATTGCAAGCTCCGCCTGCTGGGT T C METTL16 Ensembl:ENSG00000127804 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1283540826 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80864,RMVar_hsa_circ_181248,RMVar_hsa_circ_79299,RMVar_hsa_circ_181247,RMVar_hsa_circ_47384,RMVar_hsa_circ_280298,RMVar_hsa_circ_181251,RMVar_hsa_circ_346020,RMVar_hsa_circ_181255,RMVar_hsa_circ_277762,RMVar_hsa_circ_341741,RMVar_hsa_circ_287833,RMVar_hsa_circ_181256,RMVar_hsa_circ_181257,RMVar_hsa_circ_290901,RMVar_hsa_circ_354809 45865 RMVar_ID_45865 Human_SNP_ID_615017020 A-to-I Human chr17 - 2476262 2476262 2476262 CCTCCAACTCAGATTACTTTCCTTGACCTCCAATCTCATATATATGAGAAACTTGGATTTCTGAA CCTCCAACTCAGATTACTTTCCTTGACCTCCAGTCTCATATATATGAGAAACTTGGATTTCTGAA T C METTL16 Ensembl:ENSG00000127804 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1029006185 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181248,RMVar_hsa_circ_79299,RMVar_hsa_circ_47384,RMVar_hsa_circ_277762,RMVar_hsa_circ_341741,RMVar_hsa_circ_181256,RMVar_hsa_circ_354809,RMVar_hsa_circ_319667 45866 RMVar_ID_45866 Human_SNP_ID_615019558 A-to-I Human chr17 - 2486790 2486790 2486790 TTTTGTATATTTTATAGAAATAGGGTTTCACCATGCTACCCAGGTTGGTCTCAAACTCCTGGACT TTTTGTATATTTTATAGAAATAGGGTTTCACCGTGCTACCCAGGTTGGTCTCAAACTCCTGGACT T C METTL16 Ensembl:ENSG00000127804 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1174917701 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_341741,RMVar_hsa_circ_354809,RMVar_hsa_circ_319667 45867 RMVar_ID_45867 Human_SNP_ID_615023621 A-to-I Human chr17 - 2499927 2499927 2499927 CAACAAAGCAAAACCCTGTCTCTATTAAAAATACAAAAAATTAGCTGGGTGTGGTGATGCACACT CAACAAAGCAAAACCCTGTCTCTATTAAAAATGCAAAAAATTAGCTGGGTGTGGTGATGCACACT T C METTL16 Ensembl:ENSG00000127804 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs980866908 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_341741,RMVar_hsa_circ_354809,RMVar_hsa_circ_319667 45868 RMVar_ID_45868 Human_SNP_ID_615052412 A-to-I Human chr17 + 2598190 2598190 2598190 AGAATTGCTTGAACCCGGGAGGTGGAGGTTGCAATGAGCCGAGATCGCACCATTACGCTCCAGCC AGAATTGCTTGAACCCGGGAGGTGGAGGTTGCGATGAGCCGAGATCGCACCATTACGCTCCAGCC A G PAFAH1B1 Ensembl:ENSG00000007168 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1197172743 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181259,RMVar_hsa_circ_81867 45869 RMVar_ID_45869 Human_SNP_ID_615055523 A-to-I Human chr17 + 2610025 2610025 2610025 TTTTGTATTTTTAGTAGAGGCAGGGTTTCGCCATGTTGGCCATCTGGTCTTGAACTCCTGGCCTC TTTTGTATTTTTAGTAGAGGCAGGGTTTCGCCGTGTTGGCCATCTGGTCTTGAACTCCTGGCCTC A G PAFAH1B1 Ensembl:ENSG00000007168 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1467815128 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12932643 RMVar_hsa_circ_181259,RMVar_hsa_circ_81867 45870 RMVar_ID_45870 Human_SNP_ID_615058011 A-to-I Human chr17 + 2619227 2619227 2619227 GCTTTCGTGTAGCGGCGTAATCACCGCAGCTCACTGTAGACTCCAACTCCTGGGCTTAGGTGATC GCTTTCGTGTAGCGGCGTAATCACCGCAGCTCGCTGTAGACTCCAACTCCTGGGCTTAGGTGATC A G PAFAH1B1 Ensembl:ENSG00000007168 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs974890982 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12933003 RMVar_hsa_circ_181259,RMVar_hsa_circ_81867,RMVar_hsa_circ_323378 45871 RMVar_ID_45871 Human_SNP_ID_615058041 A-to-I Human chr17 + 2619370 2619370 2619370 TGTAGAGATGGGGTTTCACTAGCTGGGACTACAAGCATGTGCCACCATGCCTGGCTAATTAAAAA TGTAGAGATGGGGTTTCACTAGCTGGGACTACGAGCATGTGCCACCATGCCTGGCTAATTAAAAA A G PAFAH1B1 Ensembl:ENSG00000007168 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903715877 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6571067 RMVar_hsa_circ_181259,RMVar_hsa_circ_81867,RMVar_hsa_circ_323378 45872 RMVar_ID_45872 Human_SNP_ID_615059558 A-to-I Human chr17 + 2624757 2624757 2624757 ATATCACCTGGTTTCTCTGTGTTGCCCAGGCTAGTCTTGAACTCCTGGGCTCAAGCGATCTGCAT ATATCACCTGGTTTCTCTGTGTTGCCCAGGCTGGTCTTGAACTCCTGGGCTCAAGCGATCTGCAT A G PAFAH1B1 Ensembl:ENSG00000007168 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1194761711 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181259,RMVar_hsa_circ_81867,RMVar_hsa_circ_323378 45873 RMVar_ID_45873 Human_SNP_ID_615060192 A-to-I Human chr17 + 2626658 2626658 2626658 CTCACTGCAACCTCTGACTCCCTGGTTCAAGCAATTCAACTGCCTCAGCCTCCCAAGTAGCTGGG CTCACTGCAACCTCTGACTCCCTGGTTCAAGCGATTCAACTGCCTCAGCCTCCCAAGTAGCTGGG A G PAFAH1B1 Ensembl:ENSG00000007168 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1157641596 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181259,RMVar_hsa_circ_81867,RMVar_hsa_circ_323378 45874 RMVar_ID_45874 Human_SNP_ID_615062773 A-to-I Human chr17 + 2636771 2636771 2636771 TTCCTTTAAAAGAAATTGGGTCTCGCTTTGTCACCTAGGCTGGAGTGCAATGGCATGATCGTAGC TTCCTTTAAAAGAAATTGGGTCTCGCTTTGTCGCCTAGGCTGGAGTGCAATGGCATGATCGTAGC A G PAFAH1B1 Ensembl:ENSG00000007168 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1346813344 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12933335 RMVar_hsa_circ_181260,RMVar_hsa_circ_181259,RMVar_hsa_circ_81867,RMVar_hsa_circ_301224,RMVar_hsa_circ_323378 45875 RMVar_ID_45875 Human_SNP_ID_615064518 A-to-I Human chr17 + 2643449 2643449 2643449 CCACACTCAGCTAATTTTTCTTTAGTTTTTGTAGAGATGGTCTCACTATGTTGCCCAGGCTGCCT CCACACTCAGCTAATTTTTCTTTAGTTTTTGTGGAGATGGTCTCACTATGTTGCCCAGGCTGCCT A G PAFAH1B1 Ensembl:ENSG00000007168 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1366228529 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6571198,Human_RBP_ID_12933604,Human_RBP_ID_17566748,Human_RBP_ID_24372090 RMVar_hsa_circ_181259,RMVar_hsa_circ_81867,RMVar_hsa_circ_1407,RMVar_hsa_circ_333941,RMVar_hsa_circ_361371,RMVar_hsa_circ_372504,RMVar_hsa_circ_340063,RMVar_hsa_circ_181262,RMVar_hsa_circ_181263 45876 RMVar_ID_45876 Human_SNP_ID_615064754 A-to-I Human chr17 + 2644270 2644270 2644270 TTTTCTTTTTAAAACAGTTGTAGGCTGGGCACAGTGACTCATGCCTGTAATCCCAGCACTTTGGG TTTTCTTTTTAAAACAGTTGTAGGCTGGGCACGGTGACTCATGCCTGTAATCCCAGCACTTTGGG A G PAFAH1B1 Ensembl:ENSG00000007168 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1304806976 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12933635 RMVar_hsa_circ_181259,RMVar_hsa_circ_81867,RMVar_hsa_circ_1407,RMVar_hsa_circ_333941,RMVar_hsa_circ_361371,RMVar_hsa_circ_372504,RMVar_hsa_circ_340063,RMVar_hsa_circ_181262,RMVar_hsa_circ_181263 45877 RMVar_ID_45877 Human_SNP_ID_615064771 A-to-I Human chr17 + 2644371 2644371 2644371 CAAGACCAGCCTGGCTAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAAATGAGCCGGGC CAAGACCAGCCTGGCTAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAAATGAGCCGGGC A G PAFAH1B1 Ensembl:ENSG00000007168 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1026557878 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181259,RMVar_hsa_circ_81867,RMVar_hsa_circ_1407,RMVar_hsa_circ_333941,RMVar_hsa_circ_361371,RMVar_hsa_circ_372504,RMVar_hsa_circ_340063,RMVar_hsa_circ_181262,RMVar_hsa_circ_181263 45878 RMVar_ID_45878 Human_SNP_ID_615064981 A-to-I Human chr17 + 2645126 2645126 2645126 AAAATTAGCCGGTTGTGGTGGCAGGCACCTGTAATCCCGGCTACTCAGCTGGCTGAGGCAAGAGG AAAATTAGCCGGTTGTGGTGGCAGGCACCTGTCATCCCGGCTACTCAGCTGGCTGAGGCAAGAGG A C PAFAH1B1 Ensembl:ENSG00000007168 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1280945151 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181259,RMVar_hsa_circ_81867,RMVar_hsa_circ_1407,RMVar_hsa_circ_333941,RMVar_hsa_circ_361371,RMVar_hsa_circ_372504,RMVar_hsa_circ_340063,RMVar_hsa_circ_181262,RMVar_hsa_circ_181263 45879 RMVar_ID_45879 Human_SNP_ID_615065612 A-to-I Human chr17 + 2647469 2647469 2647469 TGAGGCGTGAGAATCACTTGAACCTGAGAGGCAGAGATTGCAGTGAGCTGAGATCATGCCACTGT TGAGGCGTGAGAATCACTTGAACCTGAGAGGCGGAGATTGCAGTGAGCTGAGATCATGCCACTGT A G PAFAH1B1 Ensembl:ENSG00000007168 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs966675049 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8447115,Human_RBP_ID_12933696 RMVar_hsa_circ_181259,RMVar_hsa_circ_81867,RMVar_hsa_circ_1407,RMVar_hsa_circ_333941,RMVar_hsa_circ_361371,RMVar_hsa_circ_372504,RMVar_hsa_circ_340063,RMVar_hsa_circ_181262,RMVar_hsa_circ_181263 45880 RMVar_ID_45880 Human_SNP_ID_615066289 A-to-I Human chr17 + 2649858 2649858 2649858 ATATACAAATATTATTGTAAAATGTGGAATAGACAAATAGGTTAGGGGAACAAAGTTCAAAGACA ATATACAAATATTATTGTAAAATGTGGAATAGGCAAATAGGTTAGGGGAACAAAGTTCAAAGACA A G PAFAH1B1 Ensembl:ENSG00000007168 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11078288 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2497839 RMVar_hsa_circ_181259,RMVar_hsa_circ_81867,RMVar_hsa_circ_1407,RMVar_hsa_circ_333941,RMVar_hsa_circ_361371,RMVar_hsa_circ_372504,RMVar_hsa_circ_340063,RMVar_hsa_circ_181262,RMVar_hsa_circ_181263 45881 RMVar_ID_45881 Human_SNP_ID_615067674 A-to-I Human chr17 + 2653872 2653872 2653872 ACTCTGTTGCCCAGGCTGGAGTACAGTGGCGCAATCTCGGCTTACTGCAACCTCCACCTCCTGGG ACTCTGTTGCCCAGGCTGGAGTACAGTGGCGCCATCTCGGCTTACTGCAACCTCCACCTCCTGGG A C PAFAH1B1 Ensembl:ENSG00000007168 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs969472352 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181259,RMVar_hsa_circ_81867,RMVar_hsa_circ_1407,RMVar_hsa_circ_333941,RMVar_hsa_circ_361371,RMVar_hsa_circ_372504,RMVar_hsa_circ_340063,RMVar_hsa_circ_181262,RMVar_hsa_circ_181263 45882 RMVar_ID_45882 Human_SNP_ID_615067846 A-to-I Human chr17 + 2654436 2654436 2654436 GACCTCAGGTGATCGCCCGCCTCAGCCTCTCAAAGTGTTGGGATTACAGGCATGAGCCACTCCAC GACCTCAGGTGATCGCCCGCCTCAGCCTCTCAGAGTGTTGGGATTACAGGCATGAGCCACTCCAC A G PAFAH1B1 Ensembl:ENSG00000007168 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs555593324 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181259,RMVar_hsa_circ_81867,RMVar_hsa_circ_1407,RMVar_hsa_circ_333941,RMVar_hsa_circ_361371,RMVar_hsa_circ_372504,RMVar_hsa_circ_340063,RMVar_hsa_circ_181262,RMVar_hsa_circ_181263 45883 RMVar_ID_45883 Human_SNP_ID_615067923 A-to-I Human chr17 + 2654711 2654711 2654711 TTACCGAGGCTGGAGTGCAGTGGCTCAATCTCAGTTCACTGCAGCCTCCGCCTCCCGGGCTCAAA TTACCGAGGCTGGAGTGCAGTGGCTCAATCTCGGTTCACTGCAGCCTCCGCCTCCCGGGCTCAAA A G PAFAH1B1 Ensembl:ENSG00000007168 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs947125617 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12933873 RMVar_hsa_circ_181259,RMVar_hsa_circ_81867,RMVar_hsa_circ_1407,RMVar_hsa_circ_333941,RMVar_hsa_circ_361371,RMVar_hsa_circ_372504,RMVar_hsa_circ_340063,RMVar_hsa_circ_181262,RMVar_hsa_circ_181263 45884 RMVar_ID_45884 Human_SNP_ID_615069202 A-to-I Human chr17 + 2659327 2659326 2659328 TTGGGAGGCCAAGGCGGGCGGATCACAAGGTCAAGAGATCGAGACCATCCTTGCCAATATGGTGA TTGGGAGGCCAAGGCGGGCGGATCACAAGGTC__GAGATCGAGACCATCCTTGCCAATATGGTGA CAA C PAFAH1B1 Ensembl:ENSG00000007168 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs756497755 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_181259,RMVar_hsa_circ_81867,RMVar_hsa_circ_1407,RMVar_hsa_circ_333941,RMVar_hsa_circ_361371,RMVar_hsa_circ_372504,RMVar_hsa_circ_340063,RMVar_hsa_circ_181262,RMVar_hsa_circ_181263 45885 RMVar_ID_45885 Human_SNP_ID_615069341 A-to-I Human chr17 + 2659716 2659716 2659716 AAAATTAGCTGGGCATGGTGGTGCTCACCTGTAATCCCAGCTACTCAGGAGGCTGAGGCATGAGA AAAATTAGCTGGGCATGGTGGTGCTCACCTGTGATCCCAGCTACTCAGGAGGCTGAGGCATGAGA A G PAFAH1B1 Ensembl:ENSG00000007168 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs960121631 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181259,RMVar_hsa_circ_81867,RMVar_hsa_circ_1407,RMVar_hsa_circ_333941,RMVar_hsa_circ_361371,RMVar_hsa_circ_372504,RMVar_hsa_circ_340063,RMVar_hsa_circ_181262,RMVar_hsa_circ_181263 45886 RMVar_ID_45886 Human_SNP_ID_615070097 A-to-I Human chr17 + 2662503 2662503 2662503 TTGGCTCACCGAAACCTTTGCCTCCCAGATTCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGC TTGGCTCACCGAAACCTTTGCCTCCCAGATTCGAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGC A G PAFAH1B1 Ensembl:ENSG00000007168 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1032964608 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181259,RMVar_hsa_circ_81867,RMVar_hsa_circ_1407,RMVar_hsa_circ_333941,RMVar_hsa_circ_361371,RMVar_hsa_circ_372504,RMVar_hsa_circ_340063,RMVar_hsa_circ_181262,RMVar_hsa_circ_181263 45887 RMVar_ID_45887 Human_SNP_ID_615070105 A-to-I Human chr17 + 2662529 2662529 2662529 AGATTCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCTCCTGCCACCATA AGATTCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCTCCTGCCACCATA A G PAFAH1B1 Ensembl:ENSG00000007168 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1254606432 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181259,RMVar_hsa_circ_81867,RMVar_hsa_circ_1407,RMVar_hsa_circ_333941,RMVar_hsa_circ_361371,RMVar_hsa_circ_372504,RMVar_hsa_circ_340063,RMVar_hsa_circ_181262,RMVar_hsa_circ_181263 45888 RMVar_ID_45888 Human_SNP_ID_615070171 A-to-I Human chr17 + 2662861 2662861 2662861 GGCCAGGTACAGTGGCTAACGCCTGTAATCCCAACACTTTGGGAGGCCAAGGTGGGCGGATCACC GGCCAGGTACAGTGGCTAACGCCTGTAATCCCCACACTTTGGGAGGCCAAGGTGGGCGGATCACC A C PAFAH1B1 Ensembl:ENSG00000007168 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1308231117 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181259,RMVar_hsa_circ_81867,RMVar_hsa_circ_1407,RMVar_hsa_circ_333941,RMVar_hsa_circ_361371,RMVar_hsa_circ_372504,RMVar_hsa_circ_340063,RMVar_hsa_circ_181262,RMVar_hsa_circ_181263 45889 RMVar_ID_45889 Human_SNP_ID_615070195 A-to-I Human chr17 + 2662966 2662966 2662966 AGAAACCCCGTCTCTACTAAAAATACAAAATTAGCTGGGCATCGTGGCACCTGCCTGTAATCCCA AGAAACCCCGTCTCTACTAAAAATACAAAATTGGCTGGGCATCGTGGCACCTGCCTGTAATCCCA A G PAFAH1B1 Ensembl:ENSG00000007168 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs985775057 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181259,RMVar_hsa_circ_81867,RMVar_hsa_circ_1407,RMVar_hsa_circ_333941,RMVar_hsa_circ_361371,RMVar_hsa_circ_372504,RMVar_hsa_circ_340063,RMVar_hsa_circ_181262,RMVar_hsa_circ_181263 45890 RMVar_ID_45890 Human_SNP_ID_615070213 A-to-I Human chr17 + 2663045 2663044 2663046 TGATGCAGGAGAATCGCTTGAACCTGGGAGACAGAGGTTGTGGTGAGCCAAGATCACGCCATTGC TGATGCAGGAGAATCGCTTGAACCTGGGAGAC__AGGTTGTGGTGAGCCAAGATCACGCCATTGC CAG C PAFAH1B1 Ensembl:ENSG00000007168 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1304116805 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_181259,RMVar_hsa_circ_81867,RMVar_hsa_circ_1407,RMVar_hsa_circ_333941,RMVar_hsa_circ_361371,RMVar_hsa_circ_372504,RMVar_hsa_circ_340063,RMVar_hsa_circ_181262,RMVar_hsa_circ_181263 45891 RMVar_ID_45891 Human_SNP_ID_615072281 A-to-I Human chr17 + 2669879 2669879 2669879 TGTCATTCCTGCTCTGAGACAGGGAGCGGACTATGTCTTGTGACTTTATATACCTTATCACTATT TGTCATTCCTGCTCTGAGACAGGGAGCGGACTGTGTCTTGTGACTTTATATACCTTATCACTATT A G PAFAH1B1 Ensembl:ENSG00000007168 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11078302 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5509 RMVar_hsa_circ_20390,RMVar_hsa_circ_181259,RMVar_hsa_circ_81867,RMVar_hsa_circ_1407,RMVar_hsa_circ_333941,RMVar_hsa_circ_361371,RMVar_hsa_circ_340063,RMVar_hsa_circ_181263,RMVar_hsa_circ_289550,RMVar_hsa_circ_312208,RMVar_hsa_circ_334522,RMVar_hsa_circ_320053,RMVar_hsa_circ_298448,RMVar_hsa_circ_181265,RMVar_hsa_circ_301340,RMVar_hsa_circ_375234,RMVar_hsa_circ_181267,RMVar_hsa_circ_181268,RMVar_hsa_circ_371404,RMVar_hsa_circ_181269 45892 RMVar_ID_45892 Human_SNP_ID_615072282 A-to-I Human chr17 + 2669879 2669879 2669879 TGTCATTCCTGCTCTGAGACAGGGAGCGGACTATGTCTTGTGACTTTATATACCTTATCACTATT TGTCATTCCTGCTCTGAGACAGGGAGCGGACTTTGTCTTGTGACTTTATATACCTTATCACTATT A T PAFAH1B1 Ensembl:ENSG00000007168 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11078302 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5509 RMVar_hsa_circ_20390,RMVar_hsa_circ_181259,RMVar_hsa_circ_81867,RMVar_hsa_circ_1407,RMVar_hsa_circ_333941,RMVar_hsa_circ_361371,RMVar_hsa_circ_340063,RMVar_hsa_circ_181263,RMVar_hsa_circ_289550,RMVar_hsa_circ_312208,RMVar_hsa_circ_334522,RMVar_hsa_circ_320053,RMVar_hsa_circ_298448,RMVar_hsa_circ_181265,RMVar_hsa_circ_301340,RMVar_hsa_circ_375234,RMVar_hsa_circ_181267,RMVar_hsa_circ_181268,RMVar_hsa_circ_371404,RMVar_hsa_circ_181269 45893 RMVar_ID_45893 Human_SNP_ID_615072767 A-to-I Human chr17 + 2671646 2671646 2671646 TTTTCTGGAGATGGCCTCTTGCTTTGTCACCCAAGCTGGAGTACAGTGGCACAATCTTTGCTCAC TTTTCTGGAGATGGCCTCTTGCTTTGTCACCCCAGCTGGAGTACAGTGGCACAATCTTTGCTCAC A C PAFAH1B1 Ensembl:ENSG00000007168 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1238757981 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12934689 RMVar_hsa_circ_181259,RMVar_hsa_circ_81867,RMVar_hsa_circ_1407,RMVar_hsa_circ_361371,RMVar_hsa_circ_340063,RMVar_hsa_circ_289550,RMVar_hsa_circ_312208,RMVar_hsa_circ_334522,RMVar_hsa_circ_298448,RMVar_hsa_circ_181265,RMVar_hsa_circ_301340,RMVar_hsa_circ_375234,RMVar_hsa_circ_181267,RMVar_hsa_circ_181268,RMVar_hsa_circ_371404,RMVar_hsa_circ_181269,RMVar_hsa_circ_87407,RMVar_hsa_circ_96249,RMVar_hsa_circ_181271,RMVar_hsa_circ_181272 45894 RMVar_ID_45894 Human_SNP_ID_615072772 A-to-I Human chr17 + 2671656 2671656 2671656 ATGGCCTCTTGCTTTGTCACCCAAGCTGGAGTACAGTGGCACAATCTTTGCTCACTGCAACCTCC ATGGCCTCTTGCTTTGTCACCCAAGCTGGAGTGCAGTGGCACAATCTTTGCTCACTGCAACCTCC A G PAFAH1B1 Ensembl:ENSG00000007168 Protein coding intron GSE38233;GSE107867;GSE107867 cultured B-cells;ASD brains,cerebellum;ASD brains,temporal_cortex - 24183664,30559470,30559470 RNA-Seq:(High) rs996964573 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181259,RMVar_hsa_circ_81867,RMVar_hsa_circ_1407,RMVar_hsa_circ_361371,RMVar_hsa_circ_340063,RMVar_hsa_circ_289550,RMVar_hsa_circ_312208,RMVar_hsa_circ_334522,RMVar_hsa_circ_298448,RMVar_hsa_circ_181265,RMVar_hsa_circ_301340,RMVar_hsa_circ_375234,RMVar_hsa_circ_181267,RMVar_hsa_circ_181268,RMVar_hsa_circ_371404,RMVar_hsa_circ_181269,RMVar_hsa_circ_87407,RMVar_hsa_circ_96249,RMVar_hsa_circ_181271,RMVar_hsa_circ_181272 45895 RMVar_ID_45895 Human_SNP_ID_615072775 A-to-I Human chr17 + 2671666 2671666 2671666 GCTTTGTCACCCAAGCTGGAGTACAGTGGCACAATCTTTGCTCACTGCAACCTCCACCTCCCAGG GCTTTGTCACCCAAGCTGGAGTACAGTGGCACGATCTTTGCTCACTGCAACCTCCACCTCCCAGG A G PAFAH1B1 Ensembl:ENSG00000007168 Protein coding intron GSE38233;GSE107867;GSE107867 cultured B-cells;ASD brains,cerebellum;ASD brains,frontal_cortex - 24183664,30559470,30559470 RNA-Seq:(High) rs1354322197 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181259,RMVar_hsa_circ_81867,RMVar_hsa_circ_1407,RMVar_hsa_circ_361371,RMVar_hsa_circ_340063,RMVar_hsa_circ_289550,RMVar_hsa_circ_312208,RMVar_hsa_circ_334522,RMVar_hsa_circ_298448,RMVar_hsa_circ_181265,RMVar_hsa_circ_301340,RMVar_hsa_circ_375234,RMVar_hsa_circ_181267,RMVar_hsa_circ_181268,RMVar_hsa_circ_371404,RMVar_hsa_circ_181269,RMVar_hsa_circ_87407,RMVar_hsa_circ_96249,RMVar_hsa_circ_181271,RMVar_hsa_circ_181272 45896 RMVar_ID_45896 Human_SNP_ID_615072785 A-to-I Human chr17 + 2671715 2671715 2671715 ACCTCCACCTCCCAGGTTCAAATGATTCTCCCACCTCAGCCTCCAAAGTAGCTGGCAATACAGGC ACCTCCACCTCCCAGGTTCAAATGATTCTCCCGCCTCAGCCTCCAAAGTAGCTGGCAATACAGGC A G PAFAH1B1 Ensembl:ENSG00000007168 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1403310633 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181259,RMVar_hsa_circ_81867,RMVar_hsa_circ_1407,RMVar_hsa_circ_361371,RMVar_hsa_circ_340063,RMVar_hsa_circ_289550,RMVar_hsa_circ_312208,RMVar_hsa_circ_334522,RMVar_hsa_circ_298448,RMVar_hsa_circ_181265,RMVar_hsa_circ_301340,RMVar_hsa_circ_375234,RMVar_hsa_circ_181267,RMVar_hsa_circ_181268,RMVar_hsa_circ_371404,RMVar_hsa_circ_181269,RMVar_hsa_circ_87407,RMVar_hsa_circ_96249,RMVar_hsa_circ_181271,RMVar_hsa_circ_181272 45897 RMVar_ID_45897 Human_SNP_ID_615072804 A-to-I Human chr17 + 2671768 2671765 2671769 GGCAATACAGGCAAGCACCACCACACCCGGCTAACTTTTTTATTTTTAGTAGAAACAGGGTTTAA GGCAATACAGGCAAGCACCACCACACCCGG____CTTTTTTATTTTTAGTAGAAACAGGGTTTAA GCTAA G PAFAH1B1 Ensembl:ENSG00000007168 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1373778058 Functional Loss DEL dbSNP153 31..34 33 - - - RMVar_hsa_circ_181259,RMVar_hsa_circ_81867,RMVar_hsa_circ_1407,RMVar_hsa_circ_361371,RMVar_hsa_circ_340063,RMVar_hsa_circ_289550,RMVar_hsa_circ_312208,RMVar_hsa_circ_334522,RMVar_hsa_circ_298448,RMVar_hsa_circ_181265,RMVar_hsa_circ_301340,RMVar_hsa_circ_375234,RMVar_hsa_circ_181267,RMVar_hsa_circ_181268,RMVar_hsa_circ_371404,RMVar_hsa_circ_181269,RMVar_hsa_circ_87407,RMVar_hsa_circ_96249,RMVar_hsa_circ_181271,RMVar_hsa_circ_181272 45898 RMVar_ID_45898 Human_SNP_ID_615072808 A-to-I Human chr17 + 2671777 2671777 2671777 GGCAAGCACCACCACACCCGGCTAACTTTTTTATTTTTAGTAGAAACAGGGTTTAACCATATTGG GGCAAGCACCACCACACCCGGCTAACTTTTTTCTTTTTAGTAGAAACAGGGTTTAACCATATTGG A C PAFAH1B1 Ensembl:ENSG00000007168 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1323599999 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12934690 RMVar_hsa_circ_181259,RMVar_hsa_circ_81867,RMVar_hsa_circ_1407,RMVar_hsa_circ_361371,RMVar_hsa_circ_340063,RMVar_hsa_circ_289550,RMVar_hsa_circ_312208,RMVar_hsa_circ_334522,RMVar_hsa_circ_298448,RMVar_hsa_circ_181265,RMVar_hsa_circ_301340,RMVar_hsa_circ_375234,RMVar_hsa_circ_181267,RMVar_hsa_circ_181268,RMVar_hsa_circ_371404,RMVar_hsa_circ_181269,RMVar_hsa_circ_87407,RMVar_hsa_circ_96249,RMVar_hsa_circ_181271,RMVar_hsa_circ_181272 45899 RMVar_ID_45899 Human_SNP_ID_615072809 A-to-I Human chr17 + 2671783 2671783 2671783 CACCACCACACCCGGCTAACTTTTTTATTTTTAGTAGAAACAGGGTTTAACCATATTGGCCAGGC CACCACCACACCCGGCTAACTTTTTTATTTTTGGTAGAAACAGGGTTTAACCATATTGGCCAGGC A G PAFAH1B1 Ensembl:ENSG00000007168 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1162421451 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12934690 RMVar_hsa_circ_181259,RMVar_hsa_circ_81867,RMVar_hsa_circ_1407,RMVar_hsa_circ_361371,RMVar_hsa_circ_340063,RMVar_hsa_circ_289550,RMVar_hsa_circ_312208,RMVar_hsa_circ_334522,RMVar_hsa_circ_298448,RMVar_hsa_circ_181265,RMVar_hsa_circ_301340,RMVar_hsa_circ_375234,RMVar_hsa_circ_181267,RMVar_hsa_circ_181268,RMVar_hsa_circ_371404,RMVar_hsa_circ_181269,RMVar_hsa_circ_87407,RMVar_hsa_circ_96249,RMVar_hsa_circ_181271,RMVar_hsa_circ_181272 45900 RMVar_ID_45900 Human_SNP_ID_615072840 A-to-I Human chr17 + 2671883 2671883 2671883 CCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAACCACTGCGCCTGGCCCACCATTTTAAAC CCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAACCACTGCGCCTGGCCCACCATTTTAAAC A G PAFAH1B1 Ensembl:ENSG00000007168 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1047241215 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12934692,Human_RBP_ID_27450011 RMVar_hsa_circ_181259,RMVar_hsa_circ_81867,RMVar_hsa_circ_1407,RMVar_hsa_circ_361371,RMVar_hsa_circ_340063,RMVar_hsa_circ_289550,RMVar_hsa_circ_312208,RMVar_hsa_circ_334522,RMVar_hsa_circ_298448,RMVar_hsa_circ_181265,RMVar_hsa_circ_301340,RMVar_hsa_circ_375234,RMVar_hsa_circ_181267,RMVar_hsa_circ_181268,RMVar_hsa_circ_371404,RMVar_hsa_circ_181269,RMVar_hsa_circ_87407,RMVar_hsa_circ_96249,RMVar_hsa_circ_181271,RMVar_hsa_circ_181272 45901 RMVar_ID_45901 Human_SNP_ID_615072870 A-to-I Human chr17 + 2672006 2672006 2672006 TATCAACCTAGAAGCTAGGCACAGTGGCTCACACCTATAATCTCAGCACTTTTGGAGGCCAAGGC TATCAACCTAGAAGCTAGGCACAGTGGCTCACGCCTATAATCTCAGCACTTTTGGAGGCCAAGGC A G PAFAH1B1 Ensembl:ENSG00000007168 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1197805523 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12934701 RMVar_hsa_circ_181259,RMVar_hsa_circ_81867,RMVar_hsa_circ_1407,RMVar_hsa_circ_361371,RMVar_hsa_circ_340063,RMVar_hsa_circ_289550,RMVar_hsa_circ_312208,RMVar_hsa_circ_334522,RMVar_hsa_circ_298448,RMVar_hsa_circ_181265,RMVar_hsa_circ_301340,RMVar_hsa_circ_375234,RMVar_hsa_circ_181267,RMVar_hsa_circ_181268,RMVar_hsa_circ_371404,RMVar_hsa_circ_181269,RMVar_hsa_circ_87407,RMVar_hsa_circ_96249,RMVar_hsa_circ_181271,RMVar_hsa_circ_181272 45902 RMVar_ID_45902 Human_SNP_ID_615072871 A-to-I Human chr17 + 2672010 2672010 2672010 AACCTAGAAGCTAGGCACAGTGGCTCACACCTATAATCTCAGCACTTTTGGAGGCCAAGGCAGGA AACCTAGAAGCTAGGCACAGTGGCTCACACCTGTAATCTCAGCACTTTTGGAGGCCAAGGCAGGA A G PAFAH1B1 Ensembl:ENSG00000007168 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1360431839 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181259,RMVar_hsa_circ_81867,RMVar_hsa_circ_1407,RMVar_hsa_circ_361371,RMVar_hsa_circ_340063,RMVar_hsa_circ_289550,RMVar_hsa_circ_312208,RMVar_hsa_circ_334522,RMVar_hsa_circ_298448,RMVar_hsa_circ_181265,RMVar_hsa_circ_301340,RMVar_hsa_circ_375234,RMVar_hsa_circ_181267,RMVar_hsa_circ_181268,RMVar_hsa_circ_371404,RMVar_hsa_circ_181269,RMVar_hsa_circ_87407,RMVar_hsa_circ_96249,RMVar_hsa_circ_181271,RMVar_hsa_circ_181272 45903 RMVar_ID_45903 Human_SNP_ID_615072875 A-to-I Human chr17 + 2672039 2672039 2672039 CCTATAATCTCAGCACTTTTGGAGGCCAAGGCAGGAAGGATTGCTTGAGGACAGGAGTTCGAGAC CCTATAATCTCAGCACTTTTGGAGGCCAAGGCGGGAAGGATTGCTTGAGGACAGGAGTTCGAGAC A G PAFAH1B1 Ensembl:ENSG00000007168 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1010137673 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181259,RMVar_hsa_circ_81867,RMVar_hsa_circ_1407,RMVar_hsa_circ_361371,RMVar_hsa_circ_340063,RMVar_hsa_circ_289550,RMVar_hsa_circ_312208,RMVar_hsa_circ_334522,RMVar_hsa_circ_298448,RMVar_hsa_circ_181265,RMVar_hsa_circ_301340,RMVar_hsa_circ_375234,RMVar_hsa_circ_181267,RMVar_hsa_circ_181268,RMVar_hsa_circ_371404,RMVar_hsa_circ_181269,RMVar_hsa_circ_87407,RMVar_hsa_circ_96249,RMVar_hsa_circ_181271,RMVar_hsa_circ_181272 45904 RMVar_ID_45904 Human_SNP_ID_615073840 A-to-I Human chr17 + 2675538 2675532 2675538 ATGTCATAAATTTGATTCTGGTGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAAGTCAAG ATGTCATAAATTTGATTCTGGTGTGGT______CGCCTGTAATCCCAGCACTTTGGGAAGTCAAG TGGCTCA T PAFAH1B1 Ensembl:ENSG00000007168 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs972241421 Functional Loss DEL dbSNP153 28..33 33 - - - RMVar_hsa_circ_7468,RMVar_hsa_circ_181259,RMVar_hsa_circ_81867,RMVar_hsa_circ_361371,RMVar_hsa_circ_340063,RMVar_hsa_circ_289550,RMVar_hsa_circ_334522,RMVar_hsa_circ_375234,RMVar_hsa_circ_181268,RMVar_hsa_circ_371404,RMVar_hsa_circ_181269,RMVar_hsa_circ_87407,RMVar_hsa_circ_96249,RMVar_hsa_circ_181271,RMVar_hsa_circ_181272,RMVar_hsa_circ_312843,RMVar_hsa_circ_319507,RMVar_hsa_circ_181274 45905 RMVar_ID_45905 Human_SNP_ID_615073848 A-to-I Human chr17 + 2675568 2675568 2675568 TCACGCCTGTAATCCCAGCACTTTGGGAAGTCAAGGCAGGAGGATCACTTGAGCCCAGGAGTTTG TCACGCCTGTAATCCCAGCACTTTGGGAAGTCGAGGCAGGAGGATCACTTGAGCCCAGGAGTTTG A G PAFAH1B1 Ensembl:ENSG00000007168 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1321057614 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12934813 RMVar_hsa_circ_7468,RMVar_hsa_circ_181259,RMVar_hsa_circ_81867,RMVar_hsa_circ_361371,RMVar_hsa_circ_340063,RMVar_hsa_circ_289550,RMVar_hsa_circ_334522,RMVar_hsa_circ_375234,RMVar_hsa_circ_181268,RMVar_hsa_circ_371404,RMVar_hsa_circ_181269,RMVar_hsa_circ_87407,RMVar_hsa_circ_96249,RMVar_hsa_circ_181271,RMVar_hsa_circ_181272,RMVar_hsa_circ_312843,RMVar_hsa_circ_319507,RMVar_hsa_circ_181274 45906 RMVar_ID_45906 Human_SNP_ID_615087403 A-to-I Human chr17 - 2711679 2711679 2711679 GGCGCGGCGGGCGGCGCGGACAGCCGAGGCGGACGCCCGCTCCCGCCACCATGGTTATCAAGACG GGCGCGGCGGGCGGCGCGGACAGCCGAGGCGGTCGCCCGCTCCCGCCACCATGGTTATCAAGACG T A CLUH Ensembl:ENSG00000132361 Protein coding 5'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) 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 45907 RMVar_ID_45907 Human_SNP_ID_615104410 A-to-I Human chr17 + 2769233 2769233 2769233 TAGCCTGGATGAGAAAGTGAAACCATTTCTCTAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA TAGCCTGGATGAGAAAGTGAAACCATTTCTCTCAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA A C RAP1GAP2 Ensembl:ENSG00000132359 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1371551665 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181292 45908 RMVar_ID_45908 Human_SNP_ID_615314959 A-to-I Human chr17 - 3539647 3539647 3539647 ACTTTATTTTATTTTATTATTGTTTTTGAGACAGGTTCTCACTCTGTTGGGCAGGCTGGAGTGCA ACTTTATTTTATTTTATTATTGTTTTTGAGACGGGTTCTCACTCTGTTGGGCAGGCTGGAGTGCA T C TRPV3 Ensembl:ENSG00000167723 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs571414330 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1761143 45909 RMVar_ID_45909 Human_SNP_ID_615324611 A-to-I Human chr17 - 3570768 3570768 3570768 CGGAGGTTGCAGTGAGCCGAGATCGCACCACTACACTCCAGCCGGGGCAACAGAACGAGACTCTG CGGAGGTTGCAGTGAGCCGAGATCGCACCACTGCACTCCAGCCGGGGCAACAGAACGAGACTCTG T C TRPV1 Ensembl:ENSG00000196689 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1438185065 Functional Loss SNV dbSNP153 33..33 33 - - - 45910 RMVar_ID_45910 Human_SNP_ID_615334334 A-to-I Human chr17 - 3598842 3598842 3598842 GTCTAAGCGGCCAGGCGCGGTGGCTCACGCCTATGATCCCAGCACTTTGGGAGGCCGAGGCAGGT GTCTAAGCGGCCAGGCGCGGTGGCTCACGCCTGTGATCCCAGCACTTTGGGAGGCCGAGGCAGGT T C AC027796.3,TRPV1 Ensembl:ENSG00000262304,Ensembl:ENSG00000196689 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1435499483 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26216,RMVar_hsa_circ_73873,RMVar_hsa_circ_73056,RMVar_hsa_circ_364415,RMVar_hsa_circ_27875,RMVar_hsa_circ_24198 45911 RMVar_ID_45911 Human_SNP_ID_615335215 A-to-I Human chr17 - 3601832 3601832 3601832 CCCAGCATATTGGGAGACTGAGGTGGGGGATCACGTGAACTCAGGAGTTTGAGACCAGTCTGGCA CCCAGCATATTGGGAGACTGAGGTGGGGGATCCCGTGAACTCAGGAGTTTGAGACCAGTCTGGCA T G AC027796.3,TRPV1,AC027796.1 Ensembl:ENSG00000262304,Ensembl:ENSG00000196689,Ensembl:ENSG00000261916 Protein coding,Protein coding,lincRNA intron,intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886977737 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12978944,Human_RBP_ID_23722560 RMVar_hsa_circ_26216,RMVar_hsa_circ_73873,RMVar_hsa_circ_73056,RMVar_hsa_circ_364415,RMVar_hsa_circ_27875,RMVar_hsa_circ_24198 45912 RMVar_ID_45912 Human_SNP_ID_615339706 A-to-I Human chr17 - 3618172 3618172 3618172 AATCCAGGAGGCAGAAGTTGCTGTGAGCTGAGATCGCGCCAGTGCACTCCAGCCTGGGCAACAGA AATCCAGGAGGCAGAAGTTGCTGTGAGCTGAGGTCGCGCCAGTGCACTCCAGCCTGGGCAACAGA T C AC027796.3,SHPK Ensembl:ENSG00000262304,Ensembl:ENSG00000197417 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs980260975 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18911 45913 RMVar_ID_45913 Human_SNP_ID_615342841 A-to-I Human chr17 - 3628826 3628826 3628826 TGGGCAACATAGTGGGACCCCATCTCTACAAAAGATGCAAAAATAAGTTGGGTGTGGTGCGACAT TGGGCAACATAGTGGGACCCCATCTCTACAAACGATGCAAAAATAAGTTGGGTGTGGTGCGACAT T G AC027796.3,SHPK Ensembl:ENSG00000262304,Ensembl:ENSG00000197417 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs568815220 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82198,RMVar_hsa_circ_181317,RMVar_hsa_circ_181319,RMVar_hsa_circ_109633,RMVar_hsa_circ_314618,RMVar_hsa_circ_181318 45914 RMVar_ID_45914 Human_SNP_ID_615344498 A-to-I Human chr17 - 3634367 3634367 3634367 TGGGGTTTCACCATGTTGGCAAGGCTGGTCTCAAACTCCTGACCTCAACTGATCTGCCTGCCTCG TGGGGTTTCACCATGTTGGCAAGGCTGGTCTCGAACTCCTGACCTCAACTGATCTGCCTGCCTCG T C AC027796.3,SHPK Ensembl:ENSG00000262304,Ensembl:ENSG00000197417 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1170551690 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25275603 RMVar_hsa_circ_109633,RMVar_hsa_circ_181318 45915 RMVar_ID_45915 Human_SNP_ID_615344659 A-to-I Human chr17 - 3634921 3634921 3634921 GTGATCTGCCCACTTCAGCCTCCCAAAGTGCTAGGATTACAGTTGTGAGTCACTGCGCCTGGCCC GTGATCTGCCCACTTCAGCCTCCCAAAGTGCTGGGATTACAGTTGTGAGTCACTGCGCCTGGCCC T C AC027796.3,SHPK Ensembl:ENSG00000262304,Ensembl:ENSG00000197417 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs996551973 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109633,RMVar_hsa_circ_181318 45916 RMVar_ID_45916 Human_SNP_ID_615344725 A-to-I Human chr17 - 3635136 3635136 3635136 ACCAAGTCTCGCTCTGTTGCCCAGGCTGGAGTACAGTGGCGTGATCTGGGCTCACTGCAACCTCC ACCAAGTCTCGCTCTGTTGCCCAGGCTGGAGTGCAGTGGCGTGATCTGGGCTCACTGCAACCTCC T C AC027796.3,SHPK Ensembl:ENSG00000262304,Ensembl:ENSG00000197417 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs112786736 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109633,RMVar_hsa_circ_181318 45917 RMVar_ID_45917 Human_SNP_ID_615353755 A-to-I Human chr17 - 3663263 3663263 3663263 GGGGACTGGACACACATCCTGCCAGAGGCGCTACGAAGCTTTGCCCAGATGAAGCCAGGTGGGCT GGGGACTGGACACACATCCTGCCAGAGGCGCTGCGAAGCTTTGCCCAGATGAAGCCAGGTGGGCT T C TAX1BP3,P2RX5-TAX1BP3 Ensembl:ENSG00000213977,Ensembl:ENSG00000257950 Protein coding,Protein coding 3'UTR,3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1006387024 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_487757,Human_RBP_ID_26458636 RMVar_hsa_circ_101574,RMVar_hsa_circ_181325 45918 RMVar_ID_45918 Human_SNP_ID_615356988 A-to-I Human chr17 - 3674165 3674165 3674165 CTGGGACTACAGGCGCTCGCCTCGCCCGGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCA CTGGGACTACAGGCGCTCGCCTCGCCCGGCTATTTTTTTGTATTTTTAGTAGAGACGGGGTTTCA T A P2RX5,P2RX5-TAX1BP3 Ensembl:ENSG00000083454,Ensembl:ENSG00000257950 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs941620677 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 45919 RMVar_ID_45919 Human_SNP_ID_615356989 A-to-I Human chr17 - 3674165 3674165 3674165 CTGGGACTACAGGCGCTCGCCTCGCCCGGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCA CTGGGACTACAGGCGCTCGCCTCGCCCGGCTACTTTTTTGTATTTTTAGTAGAGACGGGGTTTCA T G P2RX5,P2RX5-TAX1BP3 Ensembl:ENSG00000083454,Ensembl:ENSG00000257950 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs941620677 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 45920 RMVar_ID_45920 Human_SNP_ID_615357276 A-to-I Human chr17 - 3675108 3675108 3675108 TTGAACCCGGGAGACGGAGGTTGCAGTGATCCAAGATCGTGCCACTGCACTCCAGCCTGGGCGAC TTGAACCCGGGAGACGGAGGTTGCAGTGATCCGAGATCGTGCCACTGCACTCCAGCCTGGGCGAC T C P2RX5,P2RX5-TAX1BP3 Ensembl:ENSG00000083454,Ensembl:ENSG00000257950 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1251764305 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 45921 RMVar_ID_45921 Human_SNP_ID_615357427 A-to-I Human chr17 - 3675680 3675680 3675680 GGCATGGTGTCCACATGCCTGTAGTCCCAGCTACTCGGGAGGCGGAGGCAGGAGAATCGCTTGAA GGCATGGTGTCCACATGCCTGTAGTCCCAGCTGCTCGGGAGGCGGAGGCAGGAGAATCGCTTGAA T C P2RX5,P2RX5-TAX1BP3 Ensembl:ENSG00000083454,Ensembl:ENSG00000257950 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1277459501 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 45922 RMVar_ID_45922 Human_SNP_ID_615357433 A-to-I Human chr17 - 3675720 3675720 3675720 GGCAAAACCCCATCTCTACTAAAAATACAAAAATTAGCCGGGCATGGTGTCCACATGCCTGTAGT GGCAAAACCCCATCTCTACTAAAAATACAAAACTTAGCCGGGCATGGTGTCCACATGCCTGTAGT T G P2RX5,P2RX5-TAX1BP3 Ensembl:ENSG00000083454,Ensembl:ENSG00000257950 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs555402890 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 45923 RMVar_ID_45923 Human_SNP_ID_615357434 A-to-I Human chr17 - 3675722 3675722 3675722 ATGGCAAAACCCCATCTCTACTAAAAATACAAAAATTAGCCGGGCATGGTGTCCACATGCCTGTA ATGGCAAAACCCCATCTCTACTAAAAATACAAGAATTAGCCGGGCATGGTGTCCACATGCCTGTA T C P2RX5,P2RX5-TAX1BP3 Ensembl:ENSG00000083454,Ensembl:ENSG00000257950 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1217003598 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 45924 RMVar_ID_45924 Human_SNP_ID_615357442 A-to-I Human chr17 - 3675749 3675749 3675749 CAGGAGTTCGAGACCAGCCTGGCCAATATGGCAAAACCCCATCTCTACTAAAAATACAAAAATTA CAGGAGTTCGAGACCAGCCTGGCCAATATGGCGAAACCCCATCTCTACTAAAAATACAAAAATTA T C P2RX5,P2RX5-TAX1BP3 Ensembl:ENSG00000083454,Ensembl:ENSG00000257950 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1257606543 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 45925 RMVar_ID_45925 Human_SNP_ID_615357477 A-to-I Human chr17 - 3675840 3675840 3675840 CTGATTAGAAAGTAAAGATCCAGGCTGGGCGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGG CTGATTAGAAAGTAAAGATCCAGGCTGGGCGCCGTGGCTCACACCTGTAATCCCAGCACTTTGGG T G P2RX5,P2RX5-TAX1BP3 Ensembl:ENSG00000083454,Ensembl:ENSG00000257950 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs143298172 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 45926 RMVar_ID_45926 Human_SNP_ID_615357484 A-to-I Human chr17 - 3675866 3675866 3675866 AACCTGCAACAAGCCTATACTGCTCTCTGATTAGAAAGTAAAGATCCAGGCTGGGCGCAGTGGCT AACCTGCAACAAGCCTATACTGCTCTCTGATTGGAAAGTAAAGATCCAGGCTGGGCGCAGTGGCT T C P2RX5,P2RX5-TAX1BP3 Ensembl:ENSG00000083454,Ensembl:ENSG00000257950 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1005019421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12985332 RMVar_hsa_circ_97144,RMVar_hsa_circ_101574,RMVar_hsa_circ_181325,RMVar_hsa_circ_41114,RMVar_hsa_circ_181326 45927 RMVar_ID_45927 Human_SNP_ID_615357764 A-to-I Human chr17 - 3676870 3676870 3676870 TTTAGCAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTCCAACTCCTGACTTCAGGTGATC TTTAGCAGAGATGGGGTTTCACCATGTTGGCCCGGCTGGTCTCCAACTCCTGACTTCAGGTGATC T G P2RX5,P2RX5-TAX1BP3 Ensembl:ENSG00000083454,Ensembl:ENSG00000257950 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs906211077 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 45928 RMVar_ID_45928 Human_SNP_ID_615357771 A-to-I Human chr17 - 3676905 3676905 3676905 GGTGCCCACCACCATGCCCGGCTAATTTTTGTAGTTTTAGCAGAGATGGGGTTTCACCATGTTGG GGTGCCCACCACCATGCCCGGCTAATTTTTGTTGTTTTAGCAGAGATGGGGTTTCACCATGTTGG T A P2RX5,P2RX5-TAX1BP3 Ensembl:ENSG00000083454,Ensembl:ENSG00000257950 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1211646808 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 45929 RMVar_ID_45929 Human_SNP_ID_615371092 A-to-I Human chr17 - 3720694 3720694 3720694 CCCATAATTCCAGCTACTCGGGAGGCTAAGGCAGGAGAATCGCTTGAACCTGACGGGGTGGAGGT CCCATAATTCCAGCTACTCGGGAGGCTAAGGCGGGAGAATCGCTTGAACCTGACGGGGTGGAGGT T C ITGAE Ensembl:ENSG00000083457 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1375413851 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12988321 RMVar_hsa_circ_86199,RMVar_hsa_circ_181332 45930 RMVar_ID_45930 Human_SNP_ID_615371173 A-to-I Human chr17 - 3721031 3721031 3721031 TCAGCTACTCAGGAGACTGAGGTGGGAGGATCACTTGAGCCTGGAAGGTTGAGGCTATAGTGACC TCAGCTACTCAGGAGACTGAGGTGGGAGGATCCCTTGAGCCTGGAAGGTTGAGGCTATAGTGACC T G ITGAE Ensembl:ENSG00000083457 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1165371859 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86199,RMVar_hsa_circ_181332 45931 RMVar_ID_45931 Human_SNP_ID_615371322 A-to-I Human chr17 - 3721491 3721491 3721491 GGAGGATTGCTTGAGGCCAGGAGTTCAAGATCAGCCTGGGCAGCATAGTGAAACCCCATTTCTTA GGAGGATTGCTTGAGGCCAGGAGTTCAAGATCGGCCTGGGCAGCATAGTGAAACCCCATTTCTTA T C ITGAE Ensembl:ENSG00000083457 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1451866590 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86199,RMVar_hsa_circ_181332 45932 RMVar_ID_45932 Human_SNP_ID_615371324 A-to-I Human chr17 - 3721496 3721496 3721496 AGGCGGGAGGATTGCTTGAGGCCAGGAGTTCAAGATCAGCCTGGGCAGCATAGTGAAACCCCATT AGGCGGGAGGATTGCTTGAGGCCAGGAGTTCAGGATCAGCCTGGGCAGCATAGTGAAACCCCATT T C ITGAE Ensembl:ENSG00000083457 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1014782456 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86199,RMVar_hsa_circ_181332 45933 RMVar_ID_45933 Human_SNP_ID_615371423 A-to-I Human chr17 - 3721854 3721845 3721854 TTTAGTAGAGATGGGGTTTCATCGTGTTGGTCAGGCTGGTCTTGAACTCCTGACCTCAGATGATC TTTAGTAGAGATGGGGTTTCATCGTGTTGGTC_________TTGAACTCCTGACCTCAGATGATC AGACCAGCCT A ITGAE Ensembl:ENSG00000083457 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs994674361 Functional Loss DEL dbSNP153 33..41 33 - - - RMVar_hsa_circ_86199,RMVar_hsa_circ_181332 45934 RMVar_ID_45934 Human_SNP_ID_615371499 A-to-I Human chr17 - 3722116 3722116 3722116 GTTGTGCAATGGCACGATCTCGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGCGATTCTCCTG GTTGTGCAATGGCACGATCTCGGCTCACTGCAGCCTCCGCCTCCCGGGTTCAAGCGATTCTCCTG T C ITGAE Ensembl:ENSG00000083457 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1172118849 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86199,RMVar_hsa_circ_181332 45935 RMVar_ID_45935 Human_SNP_ID_615398216 A-to-I Human chr17 - 3809667 3809667 3809667 AGTTTCGCTCTTGTTGTGCAGGCTGGAGTGCAATGGCACGATCTCGGCCCACTGCAACCTCCACC AGTTTCGCTCTTGTTGTGCAGGCTGGAGTGCAGTGGCACGATCTCGGCCCACTGCAACCTCCACC T C NCBP3 Ensembl:ENSG00000074356 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs990848019 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20209152 45936 RMVar_ID_45936 Human_SNP_ID_615401072 A-to-I Human chr17 - 3820229 3820229 3820229 ATAATACACATAGGATGGGAACAGTGGCTCACACCTATAATCCCAGCACTTTGGGAGGCCAAGGC ATAATACACATAGGATGGGAACAGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCCAAGGC T C NCBP3 Ensembl:ENSG00000074356 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs748579052 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78681,RMVar_hsa_circ_328692,RMVar_hsa_circ_269867,RMVar_hsa_circ_361062,RMVar_hsa_circ_181334 45937 RMVar_ID_45937 Human_SNP_ID_615407303 A-to-I Human chr17 - 3842784 3842784 3842784 AAAATTAGTCGGGTGTGGTAGCACAGGTCTGTAGTCCCAACTACTCAAGAGGCTGAGGTGGGAGG AAAATTAGTCGGGTGTGGTAGCACAGGTCTGTGGTCCCAACTACTCAAGAGGCTGAGGTGGGAGG T C NCBP3 Ensembl:ENSG00000074356 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs74760055 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_46812,RMVar_hsa_circ_361021,RMVar_hsa_circ_181337 45938 RMVar_ID_45938 Human_SNP_ID_615413032 A-to-I Human chr17 - 3860485 3860485 3860485 TGATCGGACCCACCCTTGGAAAGCTCAGGGGTAGGCCCAGGTGGGATGCTCACCCTGTCACTGAG TGATCGGACCCACCCTTGGAAAGCTCAGGGGTGGGCCCAGGTGGGATGCTCACCCTGTCACTGAG T C CAMKK1 Ensembl:ENSG00000004660 Protein coding 3'UTR GSE100210;GSE112787 HepG2 cell line;293 Flip-In T-REx cells,empty vector - 29129909,29967493 RNA-Seq:(High) rs1044118 Functional Loss SNV dbSNP153 33..33 33 - - - 45939 RMVar_ID_45939 Human_SNP_ID_615414038 A-to-I Human chr17 - 3864371 3864371 3864371 GTGGTGGCGGGCACCTGGAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATGGCGTGAACCCG GTGGTGGCGGGCACCTGGAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCG T C CAMKK1 Ensembl:ENSG00000004660 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1365101588 Functional Loss SNV dbSNP153 33..33 33 - - - 45940 RMVar_ID_45940 Human_SNP_ID_615434836 A-to-I Human chr17 - 3931040 3931040 3931040 TGACCCCCGGGTTCAAGTGATTGTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCACGCA TGACCCCCGGGTTCAAGTGATTGTCCTGCCTCGGCCTCCCGAGTAGCTGGGATTACAGGCACGCA T C ATP2A3 Ensembl:ENSG00000074370 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1454327295 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33486,RMVar_hsa_circ_99094,RMVar_hsa_circ_181350 45941 RMVar_ID_45941 Human_SNP_ID_615435972 A-to-I Human chr17 - 3934662 3934662 3934662 AACATTAGCTGGGCGTGGTGGTGCACGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGTTGA AACATTAGCTGGGCGTGGTGGTGCACGCCTGTGATCCCAGCTACTCAGGAGGCTGAGGCAGTTGA T C ATP2A3 Ensembl:ENSG00000074370 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs928763555 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33486,RMVar_hsa_circ_99094,RMVar_hsa_circ_181350 45942 RMVar_ID_45942 Human_SNP_ID_615435973 A-to-I Human chr17 - 3934662 3934662 3934662 AACATTAGCTGGGCGTGGTGGTGCACGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGTTGA AACATTAGCTGGGCGTGGTGGTGCACGCCTGTCATCCCAGCTACTCAGGAGGCTGAGGCAGTTGA T G ATP2A3 Ensembl:ENSG00000074370 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs928763555 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33486,RMVar_hsa_circ_99094,RMVar_hsa_circ_181350 45943 RMVar_ID_45943 Human_SNP_ID_615436011 A-to-I Human chr17 - 3934795 3934795 3934795 GGGAGGGCTGGGCACGGTGGTTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGTGGA GGGAGGGCTGGGCACGGTGGTTCACGCCTGTATTCCCAGCACTTTGGGAGGCCGAGGTGGGTGGA T A ATP2A3 Ensembl:ENSG00000074370 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1416572685 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33486,RMVar_hsa_circ_99094,RMVar_hsa_circ_181350 45944 RMVar_ID_45944 Human_SNP_ID_615461769 A-to-I Human chr17 - 4023648 4023648 4023648 AATTTTTTTTTTTTTTTTTTTTTTGGAGAGACAGGGTCTTGCTAAGTTTCCCAGGCTGCTCTTGA AATTTTTTTTTTTTTTTTTTTTTTGGAGAGACGGGGTCTTGCTAAGTTTCCCAGGCTGCTCTTGA T C ZZEF1 Ensembl:ENSG00000074755 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1490668284 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_296804,RMVar_hsa_circ_23399,RMVar_hsa_circ_113203,RMVar_hsa_circ_181358,RMVar_hsa_circ_275520,RMVar_hsa_circ_56879,RMVar_hsa_circ_181361,RMVar_hsa_circ_320850,RMVar_hsa_circ_81220,RMVar_hsa_circ_116000,RMVar_hsa_circ_75454,RMVar_hsa_circ_41031,RMVar_hsa_circ_181363,RMVar_hsa_circ_181365,RMVar_hsa_circ_181364,RMVar_hsa_circ_110437,RMVar_hsa_circ_181367 45945 RMVar_ID_45945 Human_SNP_ID_615502498 A-to-I Human chr17 - 4168650 4168634 4168650 AATTAGCTGGGGGTCGTCAAAACCCTGTCTTTACTAAAAATACAAAAATTAGCTGGGGGTCGTGG AATTAGCTGGGGGTCGTCAAAACCCTGTCTTT________________TTAGCTGGGGGTCGTGG ATTTTTGTATTTTTAGT A ANKFY1 Ensembl:ENSG00000185722 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs943837759 Functional Loss DEL dbSNP153 33..48 33 - - - Human_RBP_ID_23169390 45946 RMVar_ID_45946 Human_SNP_ID_615504467 A-to-I Human chr17 - 4175692 4175692 4175692 GACGTCCCGTATGGAGAGTCCCATATCCACTCATATGTCTTATCGATCAGTGATTAGACTGGGCG GACGTCCCGTATGGAGAGTCCCATATCCACTCGTATGTCTTATCGATCAGTGATTAGACTGGGCG T C ANKFY1 Ensembl:ENSG00000185722 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4790179 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1913,RMVar_hsa_circ_20658,RMVar_hsa_circ_13957,RMVar_hsa_circ_315607,RMVar_hsa_circ_10250,RMVar_hsa_circ_358709,RMVar_hsa_circ_340909,RMVar_hsa_circ_104292,RMVar_hsa_circ_181419,RMVar_hsa_circ_65785,RMVar_hsa_circ_181417,RMVar_hsa_circ_181418,RMVar_hsa_circ_301196,RMVar_hsa_circ_374259,RMVar_hsa_circ_181420 45947 RMVar_ID_45947 Human_SNP_ID_615508407 A-to-I Human chr17 - 4190238 4190238 4190238 CAGGTTTTCACCATGTCGGCCGGGCTGATCTCAAACTGCTGGCATCAAGTAATCCGCCTGCCTCG CAGGTTTTCACCATGTCGGCCGGGCTGATCTCCAACTGCTGGCATCAAGTAATCCGCCTGCCTCG T G ANKFY1 Ensembl:ENSG00000185722 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1012220172 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13011111 RMVar_hsa_circ_6605,RMVar_hsa_circ_20658,RMVar_hsa_circ_39351,RMVar_hsa_circ_15401,RMVar_hsa_circ_80119,RMVar_hsa_circ_100380,RMVar_hsa_circ_84401,RMVar_hsa_circ_181422,RMVar_hsa_circ_181424,RMVar_hsa_circ_181423,RMVar_hsa_circ_98367,RMVar_hsa_circ_181429,RMVar_hsa_circ_181432,RMVar_hsa_circ_285559,RMVar_hsa_circ_307371,RMVar_hsa_circ_343093,RMVar_hsa_circ_181433,RMVar_hsa_circ_181431 45948 RMVar_ID_45948 Human_SNP_ID_615510686 A-to-I Human chr17 - 4198512 4198512 4198512 AAAAAATTAGCCAGGTGTGGTGGCACATGCCTATAGTCCCAGCTGCTTGGGAGGCTGAGACATGA AAAAAATTAGCCAGGTGTGGTGGCACATGCCTGTAGTCCCAGCTGCTTGGGAGGCTGAGACATGA T C ANKFY1 Ensembl:ENSG00000185722 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1262114168 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6605,RMVar_hsa_circ_20658,RMVar_hsa_circ_15401,RMVar_hsa_circ_80119,RMVar_hsa_circ_100380,RMVar_hsa_circ_84401,RMVar_hsa_circ_181422,RMVar_hsa_circ_181424,RMVar_hsa_circ_181423,RMVar_hsa_circ_98367,RMVar_hsa_circ_181429,RMVar_hsa_circ_72948,RMVar_hsa_circ_343093,RMVar_hsa_circ_181431,RMVar_hsa_circ_340149,RMVar_hsa_circ_353870,RMVar_hsa_circ_286057,RMVar_hsa_circ_181436,RMVar_hsa_circ_46461,RMVar_hsa_circ_268096,RMVar_hsa_circ_373739,RMVar_hsa_circ_264971,RMVar_hsa_circ_181438,RMVar_hsa_circ_274465,RMVar_hsa_circ_310736,RMVar_hsa_circ_311461,RMVar_hsa_circ_181439,RMVar_hsa_circ_181437 45949 RMVar_ID_45949 Human_SNP_ID_615511482 A-to-I Human chr17 - 4201811 4201811 4201811 ATAAATGGATAGCAAAAGCCTGACCTAGCCTAACCCCCTATATGCATGTTACCTGCTGCCTGCAG ATAAATGGATAGCAAAAGCCTGACCTAGCCTAGCCCCCTATATGCATGTTACCTGCTGCCTGCAG T C ANKFY1 Ensembl:ENSG00000185722 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6502775 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6605,RMVar_hsa_circ_20658,RMVar_hsa_circ_15401,RMVar_hsa_circ_80119,RMVar_hsa_circ_100380,RMVar_hsa_circ_84401,RMVar_hsa_circ_181422,RMVar_hsa_circ_181424,RMVar_hsa_circ_181423,RMVar_hsa_circ_98367,RMVar_hsa_circ_181429,RMVar_hsa_circ_72948,RMVar_hsa_circ_343093,RMVar_hsa_circ_181431,RMVar_hsa_circ_340149,RMVar_hsa_circ_353870,RMVar_hsa_circ_286057,RMVar_hsa_circ_181436,RMVar_hsa_circ_46461,RMVar_hsa_circ_268096,RMVar_hsa_circ_373739,RMVar_hsa_circ_264971,RMVar_hsa_circ_181438,RMVar_hsa_circ_274465,RMVar_hsa_circ_310736,RMVar_hsa_circ_311461,RMVar_hsa_circ_181439,RMVar_hsa_circ_181437 45950 RMVar_ID_45950 Human_SNP_ID_615513334 A-to-I Human chr17 - 4208810 4208810 4208810 AGGTGATCGATCCGCCCACCTCGGCCTCCCAAAGTGCTGGGAGTACAGGCGTGAGCCACTGCGCC AGGTGATCGATCCGCCCACCTCGGCCTCCCAATGTGCTGGGAGTACAGGCGTGAGCCACTGCGCC T A ANKFY1 Ensembl:ENSG00000185722 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1326291917 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20658,RMVar_hsa_circ_15401,RMVar_hsa_circ_80119,RMVar_hsa_circ_84401,RMVar_hsa_circ_181424,RMVar_hsa_circ_181423,RMVar_hsa_circ_48709,RMVar_hsa_circ_98367,RMVar_hsa_circ_181429,RMVar_hsa_circ_343093,RMVar_hsa_circ_181431,RMVar_hsa_circ_340149,RMVar_hsa_circ_353870,RMVar_hsa_circ_286057,RMVar_hsa_circ_181436,RMVar_hsa_circ_46461,RMVar_hsa_circ_268096,RMVar_hsa_circ_373739,RMVar_hsa_circ_181438,RMVar_hsa_circ_274465,RMVar_hsa_circ_310736,RMVar_hsa_circ_311461,RMVar_hsa_circ_181439,RMVar_hsa_circ_289640,RMVar_hsa_circ_181437,RMVar_hsa_circ_316022,RMVar_hsa_circ_282999,RMVar_hsa_circ_115372,RMVar_hsa_circ_181441,RMVar_hsa_circ_181442,RMVar_hsa_circ_181440,RMVar_hsa_circ_181444 45951 RMVar_ID_45951 Human_SNP_ID_615513504 A-to-I Human chr17 - 4209425 4209425 4209425 TCAGTGGTGCGTGCCTGTAGTCCCAGCTACTCAGGAGACTGTGGCAGGAGAATCACGTAAACCCG TCAGTGGTGCGTGCCTGTAGTCCCAGCTACTCCGGAGACTGTGGCAGGAGAATCACGTAAACCCG T G ANKFY1 Ensembl:ENSG00000185722 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1238561294 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20658,RMVar_hsa_circ_15401,RMVar_hsa_circ_80119,RMVar_hsa_circ_84401,RMVar_hsa_circ_181424,RMVar_hsa_circ_181423,RMVar_hsa_circ_48709,RMVar_hsa_circ_98367,RMVar_hsa_circ_181429,RMVar_hsa_circ_343093,RMVar_hsa_circ_181431,RMVar_hsa_circ_340149,RMVar_hsa_circ_353870,RMVar_hsa_circ_286057,RMVar_hsa_circ_181436,RMVar_hsa_circ_46461,RMVar_hsa_circ_268096,RMVar_hsa_circ_373739,RMVar_hsa_circ_181438,RMVar_hsa_circ_274465,RMVar_hsa_circ_310736,RMVar_hsa_circ_311461,RMVar_hsa_circ_181439,RMVar_hsa_circ_289640,RMVar_hsa_circ_181437,RMVar_hsa_circ_316022,RMVar_hsa_circ_282999,RMVar_hsa_circ_115372,RMVar_hsa_circ_181441,RMVar_hsa_circ_181442,RMVar_hsa_circ_181440,RMVar_hsa_circ_181444 45952 RMVar_ID_45952 Human_SNP_ID_615517914 A-to-I Human chr17 - 4226402 4226402 4226402 GTCCTGTGAATTTTTTAGTAGCTGGGACTATAAGCGCATGCCACCACACTTGACTAATTAAAAAA GTCCTGTGAATTTTTTAGTAGCTGGGACTATAGGCGCATGCCACCACACTTGACTAATTAAAAAA T C ANKFY1 Ensembl:ENSG00000185722 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs912675205 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6597028 RMVar_hsa_circ_80119,RMVar_hsa_circ_181424,RMVar_hsa_circ_48709,RMVar_hsa_circ_353870,RMVar_hsa_circ_46461,RMVar_hsa_circ_310736,RMVar_hsa_circ_181439,RMVar_hsa_circ_316022,RMVar_hsa_circ_181446,RMVar_hsa_circ_181442,RMVar_hsa_circ_316641,RMVar_hsa_circ_284066,RMVar_hsa_circ_310898,RMVar_hsa_circ_314592,RMVar_hsa_circ_181447 45953 RMVar_ID_45953 Human_SNP_ID_615521562 A-to-I Human chr17 - 4242006 4242006 4242006 CGGCTCATTGCAGCCTCTGCTTCCCAGGTTCAAGTGATTCTCTTGCCTCAGCCTCCCGAGTGGCT CGGCTCATTGCAGCCTCTGCTTCCCAGGTTCAGGTGATTCTCTTGCCTCAGCCTCCCGAGTGGCT T C ANKFY1 Ensembl:ENSG00000185722 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs976246505 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80119,RMVar_hsa_circ_181424,RMVar_hsa_circ_48709,RMVar_hsa_circ_353870,RMVar_hsa_circ_181446,RMVar_hsa_circ_316641,RMVar_hsa_circ_314592,RMVar_hsa_circ_181448,RMVar_hsa_circ_296021 45954 RMVar_ID_45954 Human_SNP_ID_615526622 A-to-I Human chr17 - 4262154 4262154 4262154 AGTAAGATCCTGTCTTAAAAAAGAGAGAGACTAGGTCACACTATGTCACCCAGGCTGGTCTCCCA AGTAAGATCCTGTCTTAAAAAAGAGAGAGACTTGGTCACACTATGTCACCCAGGCTGGTCTCCCA T A ANKFY1 Ensembl:ENSG00000185722 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs961379645 Functional Loss SNV dbSNP153 33..33 33 - - - 45955 RMVar_ID_45955 Human_SNP_ID_615526680 A-to-I Human chr17 - 4262399 4262399 4262399 AAGTTAGCCAGGTGTGGTGGCACGTGTCTGTAATTCCAGGTACTCGGGAGGATGAGGCACAAGAA AAGTTAGCCAGGTGTGGTGGCACGTGTCTGTAGTTCCAGGTACTCGGGAGGATGAGGCACAAGAA T C ANKFY1 Ensembl:ENSG00000185722 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1337928313 Functional Loss SNV dbSNP153 33..33 33 - - - 45956 RMVar_ID_45956 Human_SNP_ID_615531380 A-to-I Human chr17 - 4279728 4279728 4279728 CTGTGTCGCTCGGGCTGGATTGCAGTGGTGCAATCTCGGCTCACTGCAATCTCCGTCTCCTGGGT CTGTGTCGCTCGGGCTGGATTGCAGTGGTGCATTCTCGGCTCACTGCAATCTCCGTCTCCTGGGT T A UBE2G1 Ensembl:ENSG00000132388 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs535828126 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181450,RMVar_hsa_circ_95830,RMVar_hsa_circ_112621,RMVar_hsa_circ_181451 45957 RMVar_ID_45957 Human_SNP_ID_615531381 A-to-I Human chr17 - 4279728 4279728 4279728 CTGTGTCGCTCGGGCTGGATTGCAGTGGTGCAATCTCGGCTCACTGCAATCTCCGTCTCCTGGGT CTGTGTCGCTCGGGCTGGATTGCAGTGGTGCAGTCTCGGCTCACTGCAATCTCCGTCTCCTGGGT T C UBE2G1 Ensembl:ENSG00000132388 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs535828126 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181450,RMVar_hsa_circ_95830,RMVar_hsa_circ_112621,RMVar_hsa_circ_181451 45958 RMVar_ID_45958 Human_SNP_ID_615531600 A-to-I Human chr17 - 4280173 4280173 4280173 AAATTAGCCATGTGCAGTGGTGCACACCTGTAATCCTAGCTACTCTGGAAGCTGAGGCAGGAGAA AAATTAGCCATGTGCAGTGGTGCACACCTGTAGTCCTAGCTACTCTGGAAGCTGAGGCAGGAGAA T C UBE2G1 Ensembl:ENSG00000132388 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1421718896 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181450,RMVar_hsa_circ_95830,RMVar_hsa_circ_112621,RMVar_hsa_circ_181451 45959 RMVar_ID_45959 Human_SNP_ID_615532587 A-to-I Human chr17 - 4284062 4284062 4284062 ACGTCTGCCTCTCAGGTTCAAGCGATTCTCCCACCTCAGCTTCCCAAGTAGCTGGGACTACAGGC ACGTCTGCCTCTCAGGTTCAAGCGATTCTCCCGCCTCAGCTTCCCAAGTAGCTGGGACTACAGGC T C UBE2G1 Ensembl:ENSG00000132388 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1230832290 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181454,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_376971,RMVar_hsa_circ_285135,RMVar_hsa_circ_271444,RMVar_hsa_circ_181456,RMVar_hsa_circ_181457,RMVar_hsa_circ_181455,RMVar_hsa_circ_181453 45960 RMVar_ID_45960 Human_SNP_ID_615533271 A-to-I Human chr17 - 4286222 4286222 4286222 TTTTGTAGTTTTAGTAGAGACAGGGTTTTGCCATGTTGGCCAGGCTGGTCTCAAACTCCTGACCT TTTTGTAGTTTTAGTAGAGACAGGGTTTTGCCGTGTTGGCCAGGCTGGTCTCAAACTCCTGACCT T C UBE2G1 Ensembl:ENSG00000132388 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs773244009 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25286887 RMVar_hsa_circ_181454,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_376971,RMVar_hsa_circ_285135,RMVar_hsa_circ_271444,RMVar_hsa_circ_181456,RMVar_hsa_circ_181457,RMVar_hsa_circ_181455,RMVar_hsa_circ_181453 45961 RMVar_ID_45961 Human_SNP_ID_615533591 A-to-I Human chr17 - 4287336 4287336 4287336 GCCGTTTGGGAGGCCGAGGTGGGCAGATCACAAGGTCAGGAGTTCGAGACCAGCCTGGCCAAAGT GCCGTTTGGGAGGCCGAGGTGGGCAGATCACAGGGTCAGGAGTTCGAGACCAGCCTGGCCAAAGT T C UBE2G1 Ensembl:ENSG00000132388 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1342150377 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181454,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_376971,RMVar_hsa_circ_285135,RMVar_hsa_circ_271444,RMVar_hsa_circ_181456,RMVar_hsa_circ_181457,RMVar_hsa_circ_181455,RMVar_hsa_circ_181453 45962 RMVar_ID_45962 Human_SNP_ID_615533842 A-to-I Human chr17 - 4288367 4288367 4288367 GAAAAATTAGCCGGGCGTGGTGGCGGGCGCCTATAGTCCCAGCTACTCGGGAGGCTGAGGCAGGA GAAAAATTAGCCGGGCGTGGTGGCGGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGA T C UBE2G1 Ensembl:ENSG00000132388 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs564137627 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181454,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_376971,RMVar_hsa_circ_285135,RMVar_hsa_circ_271444,RMVar_hsa_circ_181456,RMVar_hsa_circ_181457,RMVar_hsa_circ_181455,RMVar_hsa_circ_181453 45963 RMVar_ID_45963 Human_SNP_ID_615533868 A-to-I Human chr17 - 4288455 4288455 4288455 TTGGGAGGCCGAGGCGGGTGGATCACGAGGTCAGGAGATTGAGACCATCCTGGCTAACACGGTGA TTGGGAGGCCGAGGCGGGTGGATCACGAGGTCGGGAGATTGAGACCATCCTGGCTAACACGGTGA T C UBE2G1 Ensembl:ENSG00000132388 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1383886018 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181454,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_376971,RMVar_hsa_circ_285135,RMVar_hsa_circ_271444,RMVar_hsa_circ_181456,RMVar_hsa_circ_181457,RMVar_hsa_circ_181455,RMVar_hsa_circ_181453 45964 RMVar_ID_45964 Human_SNP_ID_615533903 A-to-I Human chr17 - 4288576 4288576 4288576 TGAAATTTTTTTGTAAGCCTCATTTTAACCACAGAGCAAAGTCCTACAGTAGTTAACACAAAAGA TGAAATTTTTTTGTAAGCCTCATTTTAACCACTGAGCAAAGTCCTACAGTAGTTAACACAAAAGA T A UBE2G1 Ensembl:ENSG00000132388 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11078494 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13018620,Human_RBP_ID_22389622 RMVar_hsa_circ_181454,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_376971,RMVar_hsa_circ_285135,RMVar_hsa_circ_271444,RMVar_hsa_circ_181456,RMVar_hsa_circ_181457,RMVar_hsa_circ_181455,RMVar_hsa_circ_181453 45965 RMVar_ID_45965 Human_SNP_ID_615533904 A-to-I Human chr17 - 4288576 4288576 4288576 TGAAATTTTTTTGTAAGCCTCATTTTAACCACAGAGCAAAGTCCTACAGTAGTTAACACAAAAGA TGAAATTTTTTTGTAAGCCTCATTTTAACCACGGAGCAAAGTCCTACAGTAGTTAACACAAAAGA T C UBE2G1 Ensembl:ENSG00000132388 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11078494 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13018620,Human_RBP_ID_22389622 RMVar_hsa_circ_181454,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_376971,RMVar_hsa_circ_285135,RMVar_hsa_circ_271444,RMVar_hsa_circ_181456,RMVar_hsa_circ_181457,RMVar_hsa_circ_181455,RMVar_hsa_circ_181453 45966 RMVar_ID_45966 Human_SNP_ID_615535332 A-to-I Human chr17 - 4294069 4294069 4294069 CTTGAACTTCATTCTTTAGGCTGTGAGGACTCATTTAATTCATGACATTTAAAGCTGTACATATT CTTGAACTTCATTCTTTAGGCTGTGAGGACTCGTTTAATTCATGACATTTAAAGCTGTACATATT T C UBE2G1 Ensembl:ENSG00000132388 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs934785 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181454,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_376971,RMVar_hsa_circ_271444,RMVar_hsa_circ_181456,RMVar_hsa_circ_181457,RMVar_hsa_circ_181455,RMVar_hsa_circ_181462,RMVar_hsa_circ_333304,RMVar_hsa_circ_287872,RMVar_hsa_circ_33765,RMVar_hsa_circ_181460,RMVar_hsa_circ_181461,RMVar_hsa_circ_181459 45967 RMVar_ID_45967 Human_SNP_ID_615535668 A-to-I Human chr17 - 4294889 4294885 4294889 CATTCCGTCCTTTTTTTCTAAGACAGGGTCTCACTCTGCCACCCAGGCTGCAGTGCAATGGCATG CATTCCGTCCTTTTTTTCTAAGACAGGGTCTC____TGCCACCCAGGCTGCAGTGCAATGGCATG AGAGT A UBE2G1 Ensembl:ENSG00000132388 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1313931985 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_18942668 RMVar_hsa_circ_181454,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_376971,RMVar_hsa_circ_271444,RMVar_hsa_circ_181456,RMVar_hsa_circ_181457,RMVar_hsa_circ_181455,RMVar_hsa_circ_181462,RMVar_hsa_circ_333304,RMVar_hsa_circ_287872,RMVar_hsa_circ_33765,RMVar_hsa_circ_181460,RMVar_hsa_circ_181461,RMVar_hsa_circ_181459 45968 RMVar_ID_45968 Human_SNP_ID_615536075 A-to-I Human chr17 - 4296445 4296445 4296445 CAGCCTGGCAAACATGGTGAAACCCCATCTCTACTCAAAATACAAAAATTAGTTAGGCATGGTGG CAGCCTGGCAAACATGGTGAAACCCCATCTCTGCTCAAAATACAAAAATTAGTTAGGCATGGTGG T C UBE2G1 Ensembl:ENSG00000132388 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs942652452 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181454,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_376971,RMVar_hsa_circ_271444,RMVar_hsa_circ_181456,RMVar_hsa_circ_181457,RMVar_hsa_circ_181455,RMVar_hsa_circ_181462,RMVar_hsa_circ_333304,RMVar_hsa_circ_287872,RMVar_hsa_circ_33765,RMVar_hsa_circ_181460,RMVar_hsa_circ_181461,RMVar_hsa_circ_181459 45969 RMVar_ID_45969 Human_SNP_ID_615537663 A-to-I Human chr17 + 4302631 4302631 4302631 TTTATCTGTGGTCTTACTCTATTTTGTGAATCATGCCCAGGGTGAGAACCTAAATTATTCCACAA TTTATCTGTGGTCTTACTCTATTTTGTGAATCGTGCCCAGGGTGAGAACCTAAATTATTCCACAA A G MFSD1P1 Ensembl:ENSG00000261868 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1211534620 Functional Loss SNV dbSNP153 33..33 33 - - - 45970 RMVar_ID_45970 Human_SNP_ID_615541241 A-to-I Human chr17 - 4316084 4316084 4316084 GGTCTTGGCAAAGTACACTTAGGCGGTGGCTCACGCTTGTAATCCCAGCACTTTGAGAGGCCGAG GGTCTTGGCAAAGTACACTTAGGCGGTGGCTCGCGCTTGTAATCCCAGCACTTTGAGAGGCCGAG T C UBE2G1 Ensembl:ENSG00000132388 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs973232195 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95830,RMVar_hsa_circ_181451,RMVar_hsa_circ_181458,RMVar_hsa_circ_305510,RMVar_hsa_circ_181457,RMVar_hsa_circ_33765,RMVar_hsa_circ_338088,RMVar_hsa_circ_181459,RMVar_hsa_circ_181468,RMVar_hsa_circ_377756,RMVar_hsa_circ_344151,RMVar_hsa_circ_306396,RMVar_hsa_circ_181467 45971 RMVar_ID_45971 Human_SNP_ID_615547239 A-to-I Human chr17 - 4339433 4339433 4339433 GATCGTGGTCGTGGGTGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATTGCTTGAA GATCGTGGTCGTGGGTGCCTGTAATCCCAGCTGCTTGGGAGGCTGAGGCAGGAGAATTGCTTGAA T C UBE2G1 Ensembl:ENSG00000132388 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1383078996 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95830,RMVar_hsa_circ_181451,RMVar_hsa_circ_181468,RMVar_hsa_circ_377756 45972 RMVar_ID_45972 Human_SNP_ID_615547253 A-to-I Human chr17 - 4339479 4339479 4339479 GTCAACATGCTGAAACCCCGTCTCTACTAAATACAAAAAATTAGCCGATCGTGGTCGTGGGTGCC GTCAACATGCTGAAACCCCGTCTCTACTAAATGCAAAAAATTAGCCGATCGTGGTCGTGGGTGCC T C UBE2G1 Ensembl:ENSG00000132388 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054481704 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95830,RMVar_hsa_circ_181451,RMVar_hsa_circ_181468,RMVar_hsa_circ_377756 45973 RMVar_ID_45973 Human_SNP_ID_615547317 A-to-I Human chr17 - 4339727 4339727 4339727 CTGTGGCCTCAGCCTCCCGAGTAGCTGGCATTACAGGCATGTGCCACCACCTGCCTAATTTTGTA CTGTGGCCTCAGCCTCCCGAGTAGCTGGCATTCCAGGCATGTGCCACCACCTGCCTAATTTTGTA T G UBE2G1 Ensembl:ENSG00000132388 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs914748156 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95830,RMVar_hsa_circ_181451,RMVar_hsa_circ_181468,RMVar_hsa_circ_377756 45974 RMVar_ID_45974 Human_SNP_ID_615548637 A-to-I Human chr17 - 4344608 4344608 4344608 CTCTGGCCTCAGCCTCCCAAAGTGCTAGGATTACAGGTGTGAGTCACCGCACCTGGCTGAGAGCT CTCTGGCCTCAGCCTCCCAAAGTGCTAGGATTGCAGGTGTGAGTCACCGCACCTGGCTGAGAGCT T C UBE2G1 Ensembl:ENSG00000132388 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1055360970 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25287697 RMVar_hsa_circ_95830,RMVar_hsa_circ_181451,RMVar_hsa_circ_181468,RMVar_hsa_circ_377756 45975 RMVar_ID_45975 Human_SNP_ID_615549996 A-to-I Human chr17 - 4349273 4349273 4349273 ATGGTAGTCCTAGGCTGGAGTGCAGTGGTGCAAATTTGGCTCACTGCAACCTCTGCCTCCCGGGT ATGGTAGTCCTAGGCTGGAGTGCAGTGGTGCATATTTGGCTCACTGCAACCTCTGCCTCCCGGGT T A UBE2G1 Ensembl:ENSG00000132388 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs528622241 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13023970 RMVar_hsa_circ_95830,RMVar_hsa_circ_181451,RMVar_hsa_circ_181468,RMVar_hsa_circ_377756 45976 RMVar_ID_45976 Human_SNP_ID_615549997 A-to-I Human chr17 - 4349273 4349273 4349273 ATGGTAGTCCTAGGCTGGAGTGCAGTGGTGCAAATTTGGCTCACTGCAACCTCTGCCTCCCGGGT ATGGTAGTCCTAGGCTGGAGTGCAGTGGTGCACATTTGGCTCACTGCAACCTCTGCCTCCCGGGT T G UBE2G1 Ensembl:ENSG00000132388 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs528622241 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13023970 RMVar_hsa_circ_95830,RMVar_hsa_circ_181451,RMVar_hsa_circ_181468,RMVar_hsa_circ_377756 45977 RMVar_ID_45977 Human_SNP_ID_615550222 A-to-I Human chr17 - 4350054 4350054 4350054 CTGGGTGCAGTGACTTAACTTCTGTAATCCCAACATTTTGGGAGGCCGAGGCAGGAGGATTGCTT CTGGGTGCAGTGACTTAACTTCTGTAATCCCACCATTTTGGGAGGCCGAGGCAGGAGGATTGCTT T G UBE2G1 Ensembl:ENSG00000132388 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1461006041 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8453873,Human_RBP_ID_13024171 RMVar_hsa_circ_95830,RMVar_hsa_circ_181451,RMVar_hsa_circ_181468,RMVar_hsa_circ_377756 45978 RMVar_ID_45978 Human_SNP_ID_615551654 A-to-I Human chr17 - 4355175 4355175 4355175 CAACATGGTGAAACCCCATTTCTACTAAGAATACAAAAATTAGCTGGTCGTGGTTGCACATGCCT CAACATGGTGAAACCCCATTTCTACTAAGAATGCAAAAATTAGCTGGTCGTGGTTGCACATGCCT T C UBE2G1 Ensembl:ENSG00000132388 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1406079003 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95830,RMVar_hsa_circ_181451,RMVar_hsa_circ_181468,RMVar_hsa_circ_377756 45979 RMVar_ID_45979 Human_SNP_ID_615551668 A-to-I Human chr17 - 4355240 4355240 4355240 CCAGAACTTTGGGAGGCCGAGGCAGGTGGATCACCTGAGGTCAGGAGTTTGAGATAAGCCATGGC CCAGAACTTTGGGAGGCCGAGGCAGGTGGATCCCCTGAGGTCAGGAGTTTGAGATAAGCCATGGC T G UBE2G1 Ensembl:ENSG00000132388 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1479038350 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95830,RMVar_hsa_circ_181451,RMVar_hsa_circ_181468,RMVar_hsa_circ_377756 45980 RMVar_ID_45980 Human_SNP_ID_615554563 A-to-I Human chr17 - 4364493 4364493 4364493 ACGAGGTCAGGAGATCGAGACCATCCTGGCTAACACGGGGAAACCCTTTCTCTACTAAAAATCCA ACGAGGTCAGGAGATCGAGACCATCCTGGCTACCACGGGGAAACCCTTTCTCTACTAAAAATCCA T G UBE2G1 Ensembl:ENSG00000132388 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1473634714 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95830,RMVar_hsa_circ_181451,RMVar_hsa_circ_181468,RMVar_hsa_circ_377756 45981 RMVar_ID_45981 Human_SNP_ID_615554642 A-to-I Human chr17 - 4364704 4364704 4364704 GTGGCGGAGGGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCGGGAGAATTGCTTGAACGCG GTGGCGGAGGGCGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCGGGAGAATTGCTTGAACGCG T C UBE2G1 Ensembl:ENSG00000132388 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1276694112 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95830,RMVar_hsa_circ_181451,RMVar_hsa_circ_181468,RMVar_hsa_circ_377756 45982 RMVar_ID_45982 Human_SNP_ID_615554643 A-to-I Human chr17 - 4364704 4364704 4364704 GTGGCGGAGGGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCGGGAGAATTGCTTGAACGCG GTGGCGGAGGGCGCCTGTAATCCCAGCTACTCCGGAGGCTGAGGCGGGAGAATTGCTTGAACGCG T G UBE2G1 Ensembl:ENSG00000132388 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1276694112 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95830,RMVar_hsa_circ_181451,RMVar_hsa_circ_181468,RMVar_hsa_circ_377756 45983 RMVar_ID_45983 Human_SNP_ID_615585344 A-to-I Human chr17 + 4463242 4463242 4463242 CAACATGGTGAAACCCTGTCTCTACTGGAAATACAGAAATTAGCCAGGCATGGTGGTGGCACCTG CAACATGGTGAAACCCTGTCTCTACTGGAAATGCAGAAATTAGCCAGGCATGGTGGTGGCACCTG A G SPNS3 Ensembl:ENSG00000182557 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1319567839 Functional Loss SNV dbSNP153 33..33 33 - - - 45984 RMVar_ID_45984 Human_SNP_ID_615585345 A-to-I Human chr17 + 4463247 4463247 4463247 TGGTGAAACCCTGTCTCTACTGGAAATACAGAAATTAGCCAGGCATGGTGGTGGCACCTGTAATC TGGTGAAACCCTGTCTCTACTGGAAATACAGACATTAGCCAGGCATGGTGGTGGCACCTGTAATC A C SPNS3 Ensembl:ENSG00000182557 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs907554816 Functional Loss SNV dbSNP153 33..33 33 - - - 45985 RMVar_ID_45985 Human_SNP_ID_615611138 A-to-I Human chr17 - 4543076 4543076 4543076 CCTGCACGCCCAGGTGGAGCGGTTGGTGCAGCAGGCTGGCCGCCAGCCCGACTCCCCCACCGCCC CCTGCACGCCCAGGTGGAGCGGTTGGTGCAGCGGGCTGGCCGCCAGCCCGACTCCCCCACCGCCC T C MYBBP1A Ensembl:ENSG00000132382 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1337222061 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_236179,Human_RBP_ID_22585122 Human_Splice_Rec_1763352,Human_Splice_Rec_1763414,Human_Splice_Rec_1763466,Human_Splice_Rec_1763494 Human_miRNA_ID_2398270,Human_miRNA_ID_2512856,Human_miRNA_ID_3055679 RMVar_hsa_circ_43361,RMVar_hsa_circ_108950,RMVar_hsa_circ_181470 45986 RMVar_ID_45986 Human_SNP_ID_615611768 A-to-I Human chr17 - 4544538 4544535 4544538 TGAGCATCATCCGGCGCAGCCTGCGCAGCAGCAGCTCCAAACAGGAGCAGGACCTTCTGCACAAG TGAGCATCATCCGGCGCAGCCTGCGCAGCAGC___TCCAAACAGGAGCAGGACCTTCTGCACAAG AGCT A MYBBP1A Ensembl:ENSG00000132382 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs771197815 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_47991,Human_RBP_ID_6603580 Human_Splice_Rec_1763351,Human_Splice_Rec_1763413,Human_Splice_Rec_1763465,Human_Splice_Rec_1763493 RMVar_hsa_circ_43361,RMVar_hsa_circ_108950,RMVar_hsa_circ_181470 45987 RMVar_ID_45987 Human_SNP_ID_615639419 A-to-I Human chr17 - 4634435 4634435 4634435 GGCCAGGCACGGTGGTTCACGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCG GGCCAGGCACGGTGGTTCACGCCTGTAATCCCGGCTACTCGGGAGGCTGAGGCAGGAGAATCGCG T C ALOX15 Ensembl:ENSG00000161905 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs993318318 Functional Loss SNV dbSNP153 33..33 33 - - - 45988 RMVar_ID_45988 Human_SNP_ID_615639421 A-to-I Human chr17 - 4634440 4634436 4634440 AAGGAGGCCAGGCACGGTGGTTCACGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAA AAGGAGGCCAGGCACGGTGGTTCACGCCTGTA____CAGCTACTCGGGAGGCTGAGGCAGGAGAA GGGAT G ALOX15 Ensembl:ENSG00000161905 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1263275836 Functional Loss DEL dbSNP153 33..36 33 - - - 45989 RMVar_ID_45989 Human_SNP_ID_615639422 A-to-I Human chr17 - 4634441 4634439 4634441 AAAGGAGGCCAGGCACGGTGGTTCACGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAGGAGGCCAGGCACGGTGGTTCACGCCTGT__TCCCAGCTACTCGGGAGGCTGAGGCAGGAGA ATT A ALOX15 Ensembl:ENSG00000161905 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1418537026 Functional Loss DEL dbSNP153 33..34 33 - - - 45990 RMVar_ID_45990 Human_SNP_ID_615639422 A-to-I Human chr17 - 4634440 4634439 4634441 AAGGAGGCCAGGCACGGTGGTTCACGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAA AAGGAGGCCAGGCACGGTGGTTCACGCCTGT__TCCCAGCTACTCGGGAGGCTGAGGCAGGAGAA ATT A ALOX15 Ensembl:ENSG00000161905 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1418537026 Functional Loss DEL dbSNP153 32..33 33 - - - 45991 RMVar_ID_45991 Human_SNP_ID_615639423 A-to-I Human chr17 - 4634441 4634441 4634441 AAAGGAGGCCAGGCACGGTGGTTCACGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAGGAGGCCAGGCACGGTGGTTCACGCCTGTTATCCCAGCTACTCGGGAGGCTGAGGCAGGAGA T A ALOX15 Ensembl:ENSG00000161905 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs955226346 Functional Loss SNV dbSNP153 33..33 33 - - - 45992 RMVar_ID_45992 Human_SNP_ID_615656288 A-to-I Human chr17 - 4685605 4685605 4685605 CATTTTTTTTTGTACAGATGGGTTCTTGCTATATTGTCCAGGCTGGTCTCGAACTTCTGGGCTCA CATTTTTTTTTGTACAGATGGGTTCTTGCTATGTTGTCCAGGCTGGTCTCGAACTTCTGGGCTCA T C PELP1 Ensembl:ENSG00000141456 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037934217 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102442,RMVar_hsa_circ_2725,RMVar_hsa_circ_181482,RMVar_hsa_circ_77829,RMVar_hsa_circ_120228,RMVar_hsa_circ_181494,RMVar_hsa_circ_181496,RMVar_hsa_circ_304205,RMVar_hsa_circ_181501 45993 RMVar_ID_45993 Human_SNP_ID_615659629 A-to-I Human chr17 - 4698149 4698149 4698149 CAGCAAGAATACTGCAGAAGTCGTCCAGGTGCAGTGGCTCATGCCTGTTATCCCAGCATGAGATT CAGCAAGAATACTGCAGAAGTCGTCCAGGTGCGGTGGCTCATGCCTGTTATCCCAGCATGAGATT T C PELP1 Ensembl:ENSG00000141456 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1203727951 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13050848 45994 RMVar_ID_45994 Human_SNP_ID_615660391 A-to-I Human chr17 - 4700813 4700813 4700813 TCAAGTAATCCTTCCACCTCAGCCTCCCGAGTAGCTGGGACTACAGGTGTGCCACCACCCCTGGC TCAAGTAATCCTTCCACCTCAGCCTCCCGAGTCGCTGGGACTACAGGTGTGCCACCACCCCTGGC T G PELP1 Ensembl:ENSG00000141456 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs533409918 Functional Loss SNV dbSNP153 33..33 33 - - - 45995 RMVar_ID_45995 Human_SNP_ID_615673346 A-to-I Human chr17 - 4739737 4739737 4739737 GTGCAGCCGCCTCACAGGTCGGCGGACGGGCCAGGCGGGCGGCCTCCTGAACCGAACCGAATCGG GTGCAGCCGCCTCACAGGTCGGCGGACGGGCCGGGCGGGCGGCCTCCTGAACCGAACCGAATCGG T C CXCL16 Ensembl:ENSG00000161921 Protein coding 5'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1049760734 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_822062,Human_RBP_ID_4464244,Human_RBP_ID_5238058 RMVar_hsa_circ_124118,RMVar_hsa_circ_181507 45996 RMVar_ID_45996 Human_SNP_ID_615687246 A-to-I Human chr17 - 4787583 4787583 4787583 GCAGTGAGCCGAGATGGCGTCACTGCACTCCAACCTGGGCAACAGAGTGAGACTTCGTCTCAAAA GCAGTGAGCCGAGATGGCGTCACTGCACTCCAGCCTGGGCAACAGAGTGAGACTTCGTCTCAAAA T C lnc-VMO1-1,lnc-VMO1-1:2 RNACentral:URS00009BB8E4,RNACentral:URS00009B26D6 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1336400977 Functional Loss SNV dbSNP153 33..33 33 - - - 45997 RMVar_ID_45997 Human_SNP_ID_615696015 A-to-I Human chr17 - 4815772 4815772 4815772 TGATGGGCCCACAACGTCACTTGGTCTGGGTGACGCATCACCTGGAGCAGGCATGGAGGGTTCAT TGATGGGCCCACAACGTCACTTGGTCTGGGTGCCGCATCACCTGGAGCAGGCATGGAGGGTTCAT T G - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs752110673 Functional Loss SNV dbSNP153 33..33 33 - - - 45998 RMVar_ID_45998 Human_SNP_ID_615730681 A-to-I Human chr17 - 4927251 4927251 4927251 CCTGACCAACGTGGTGAAACCCCATCTCCACTAAAGATACAAAAATTAGCCGGGTGTGGTGGCTC CCTGACCAACGTGGTGAAACCCCATCTCCACTGAAGATACAAAAATTAGCCGGGTGTGGTGGCTC T C CHRNE Ensembl:ENSG00000108556 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs907676307 Functional Loss SNV dbSNP153 33..33 33 - - - 45999 RMVar_ID_45999 Human_SNP_ID_615730825 A-to-I Human chr17 - 4928012 4928012 4928012 GCCATCATGGCTCACTGCAGCCTCAACCTCCCAGGCTCAAGCGATCTTCCCACCTCAGTCTCCTG GCCATCATGGCTCACTGCAGCCTCAACCTCCCGGGCTCAAGCGATCTTCCCACCTCAGTCTCCTG T C CHRNE Ensembl:ENSG00000108556 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1281744587 Functional Loss SNV dbSNP153 33..33 33 - - - 46000 RMVar_ID_46000 Human_SNP_ID_615730834 A-to-I Human chr17 - 4928065 4928065 4928065 TGGTGTGATTTGAGACAGGGTCTCACTTTGTCACCCAGGTGGAATACAGTGGTGCCATCATGGCT TGGTGTGATTTGAGACAGGGTCTCACTTTGTCTCCCAGGTGGAATACAGTGGTGCCATCATGGCT T A CHRNE Ensembl:ENSG00000108556 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1023442416 Functional Loss SNV dbSNP153 33..33 33 - - - 46001 RMVar_ID_46001 Human_SNP_ID_615731087 A-to-I Human chr17 - 4928985 4928985 4928985 TTTCGTATTTTTAGTAGAGAGGGCATTTCACCATGTTGGCCAGGATGGTCTTGATCTCTTTTTTC TTTCGTATTTTTAGTAGAGAGGGCATTTCACCTTGTTGGCCAGGATGGTCTTGATCTCTTTTTTC T A CHRNE Ensembl:ENSG00000108556 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1387546235 Functional Loss SNV dbSNP153 33..33 33 - - - 46002 RMVar_ID_46002 Human_SNP_ID_615731088 A-to-I Human chr17 - 4928985 4928985 4928985 TTTCGTATTTTTAGTAGAGAGGGCATTTCACCATGTTGGCCAGGATGGTCTTGATCTCTTTTTTC TTTCGTATTTTTAGTAGAGAGGGCATTTCACCCTGTTGGCCAGGATGGTCTTGATCTCTTTTTTC T G CHRNE Ensembl:ENSG00000108556 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1387546235 Functional Loss SNV dbSNP153 33..33 33 - - - 46003 RMVar_ID_46003 Human_SNP_ID_615731089 A-to-I Human chr17 - 4929002 4929002 4929002 CACCACGCCGGGCTAATTTTCGTATTTTTAGTAGAGAGGGCATTTCACCATGTTGGCCAGGATGG CACCACGCCGGGCTAATTTTCGTATTTTTAGTGGAGAGGGCATTTCACCATGTTGGCCAGGATGG T C CHRNE Ensembl:ENSG00000108556 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1015789957 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13064662 46004 RMVar_ID_46004 Human_SNP_ID_615731668 A-to-I Human chr17 - 4931283 4931283 4931283 TTGGTCAGCCTGGTCTCGAACTCCTCATCTCAAGTGATCCACCCACATTGGCTTCCCGAAGTGCT TTGGTCAGCCTGGTCTCGAACTCCTCATCTCAGGTGATCCACCCACATTGGCTTCCCGAAGTGCT T C CHRNE Ensembl:ENSG00000108556 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417655404 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13064710,Human_RBP_ID_20233435 46005 RMVar_ID_46005 Human_SNP_ID_615741937 A-to-I Human chr17 + 4959347 4959347 4959347 CCACCTGTGCATTCACACTCTCACACACACACACACATGCCACGCACATATCCAAGCTCCAACGG CCACCTGTGCATTCACACTCTCACACACACACGCACATGCCACGCACATATCCAAGCTCCAACGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs554511561 Functional Loss SNV dbSNP153 33..33 33 - - - 46006 RMVar_ID_46006 Human_SNP_ID_615748574 A-to-I Human chr17 - 4980242 4980242 4980242 CCTAGGCCTTCCATGAGTTTGGCAGTGGTTGTAGGCACTGAGCCTTCTGCCCCACCAGCTCCTCC CCTAGGCCTTCCATGAGTTTGGCAGTGGTTGTGGGCACTGAGCCTTCTGCCCCACCAGCTCCTCC T C CAMTA2 Ensembl:ENSG00000108509 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs574932958 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5129422,Human_RBP_ID_13068801,Human_RBP_ID_23734561 RMVar_hsa_circ_120129,RMVar_hsa_circ_181571,RMVar_hsa_circ_87430,RMVar_hsa_circ_181572 46007 RMVar_ID_46007 Human_SNP_ID_615749592 A-to-I Human chr17 - 4983646 4983646 4983646 CTGGGGGGCGGAGGTTGCAGTGAGCTGAGATCATGCCATTGCACTCCAGCCTGGGTGACAGAGTA CTGGGGGGCGGAGGTTGCAGTGAGCTGAGATCGTGCCATTGCACTCCAGCCTGGGTGACAGAGTA T C CAMTA2 Ensembl:ENSG00000108509 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1284602189 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9867429,Human_RBP_ID_23170498,Human_RBP_ID_25299803 RMVar_hsa_circ_63268,RMVar_hsa_circ_181573 46008 RMVar_ID_46008 Human_SNP_ID_615749617 A-to-I Human chr17 - 4983748 4983748 4983748 GAAACCCCGTTTCTACTAAAAATACAAAAATTAGCTGGGCACGGTGGCAAGTGCCTGTAATCGCA GAAACCCCGTTTCTACTAAAAATACAAAAATTGGCTGGGCACGGTGGCAAGTGCCTGTAATCGCA T C CAMTA2 Ensembl:ENSG00000108509 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs967479410 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1765977 RMVar_hsa_circ_63268,RMVar_hsa_circ_181573 46009 RMVar_ID_46009 Human_SNP_ID_615750111 A-to-I Human chr17 - 4985561 4985561 4985561 AAAGCAGCCAGGCGTGGTGATGTACGCCTGTAATCCCAGCTACTCGAGAGGCTGAGGCGGGAGAA AAAGCAGCCAGGCGTGGTGATGTACGCCTGTAGTCCCAGCTACTCGAGAGGCTGAGGCGGGAGAA T C CAMTA2 Ensembl:ENSG00000108509 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1359095666 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63268,RMVar_hsa_circ_181573 46010 RMVar_ID_46010 Human_SNP_ID_615750112 A-to-I Human chr17 - 4985562 4985562 4985562 AAAAGCAGCCAGGCGTGGTGATGTACGCCTGTAATCCCAGCTACTCGAGAGGCTGAGGCGGGAGA AAAAGCAGCCAGGCGTGGTGATGTACGCCTGTGATCCCAGCTACTCGAGAGGCTGAGGCGGGAGA T C CAMTA2 Ensembl:ENSG00000108509 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1018833226 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63268,RMVar_hsa_circ_181573 46011 RMVar_ID_46011 Human_SNP_ID_615751512 A-to-I Human chr17 + 4989935 4989935 4989935 ATGTGCTGCTCCTCCAGCCAAGTGGGGCTGTGAAGAACAAAAAGGGGGCTATAAGTGCAGAGGGG ATGTGCTGCTCCTCCAGCCAAGTGGGGCTGTGCAGAACAAAAAGGGGGCTATAAGTGCAGAGGGG A C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1193478333 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17895853 46012 RMVar_ID_46012 Human_SNP_ID_615751861 A-to-I Human chr17 + 4991064 4991064 4991064 CCTCAGCCTCCCGAGTAGCTGGGATTACAGGCACCCACTACCACGCCCGGCCAATTTTGTATTTT CCTCAGCCTCCCGAGTAGCTGGGATTACAGGCGCCCACTACCACGCCCGGCCAATTTTGTATTTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs764746834 Functional Loss SNV dbSNP153 33..33 33 - - - 46013 RMVar_ID_46013 Human_SNP_ID_615751924 A-to-I Human chr17 + 4991293 4991293 4991293 GCTTCAAAGCCATCCTAGGCCGCAGGTTGGACAAGCTTGCTTTATACCTCATAGTTAGAGAAGGT GCTTCAAAGCCATCCTAGGCCGCAGGTTGGACGAGCTTGCTTTATACCTCATAGTTAGAGAAGGT A G lnc-KIF1C-1 RNACentral:URS0000D59F3D lincRNA intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs538263160 Functional Loss SNV dbSNP153 33..33 33 - - - 46014 RMVar_ID_46014 Human_SNP_ID_615757805 A-to-I Human chr17 + 5009380 5009380 5009380 ATTTTGTATTTTTAGTAGAGATGGGGTTCACTATGTTGGCCGGAGTGGTCTTGAACTTCTGACCT ATTTTGTATTTTTAGTAGAGATGGGGTTCACTGTGTTGGCCGGAGTGGTCTTGAACTTCTGACCT A G KIF1C Ensembl:ENSG00000129250 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs571750347 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17565745 Clinvar_Rec_129 RMVar_hsa_circ_3667,RMVar_hsa_circ_113010,RMVar_hsa_circ_181578,RMVar_hsa_circ_89684,RMVar_hsa_circ_181581,RMVar_hsa_circ_84192,RMVar_hsa_circ_52813,RMVar_hsa_circ_181583,RMVar_hsa_circ_305052 46015 RMVar_ID_46015 Human_SNP_ID_615762588 A-to-I Human chr17 + 5025073 5025073 5025073 CTGTTTTTTTTGTAGTGACGAGGTTTCACCATATTGGCCAGGCTGGTCTCGAACTCCTGATGACC CTGTTTTTTTTGTAGTGACGAGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGATGACC A G KIF1C Ensembl:ENSG00000129250 Protein coding 3'UTR GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,29796672,31158229,31158229,31158229 RNA-Seq:(High) rs763555652 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1806424 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 46016 RMVar_ID_46016 Human_SNP_ID_615762616 A-to-I Human chr17 + 5025148 5025148 5025148 CGCCCACCTTGGCCTCCCAAAGTGGTGGGATTACAGGTGTGAGCCACCGCGCCCGGCCTCCCCTG CGCCCACCTTGGCCTCCCAAAGTGGTGGGATTGCAGGTGTGAGCCACCGCGCCCGGCCTCCCCTG A G KIF1C Ensembl:ENSG00000129250 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs147286771 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2450917 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 46017 RMVar_ID_46017 Human_SNP_ID_615762719 A-to-I Human chr17 + 5025546 5025546 5025546 ATTTGTGTTAAGACTGTTTGTTGGCCAGGCGCAGTGGTTCACGCCTGTAATGCCAGCACTGGGAG ATTTGTGTTAAGACTGTTTGTTGGCCAGGCGCGGTGGTTCACGCCTGTAATGCCAGCACTGGGAG A G KIF1C Ensembl:ENSG00000129250 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1321949762 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13072911 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 46018 RMVar_ID_46018 Human_SNP_ID_615762727 A-to-I Human chr17 + 5025562 5025562 5025562 TTTGTTGGCCAGGCGCAGTGGTTCACGCCTGTAATGCCAGCACTGGGAGGCCGAGGCAGGTGGAT TTTGTTGGCCAGGCGCAGTGGTTCACGCCTGTGATGCCAGCACTGGGAGGCCGAGGCAGGTGGAT A G KIF1C Ensembl:ENSG00000129250 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs536388287 Functional Loss SNV dbSNP153 33..33 33 - - - 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 46019 RMVar_ID_46019 Human_SNP_ID_615762965 A-to-I Human chr17 + 5026478 5026478 5026478 ATAATTTTAAAAATCCACTTATGGCTGGGCACAGAAGCTCACACCTGTAATCCCAGCACTTTGGG ATAATTTTAAAAATCCACTTATGGCTGGGCACCGAAGCTCACACCTGTAATCCCAGCACTTTGGG A C KIF1C Ensembl:ENSG00000129250 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1296281792 Functional Loss SNV dbSNP153 33..33 33 - - - 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 46020 RMVar_ID_46020 Human_SNP_ID_615762987 A-to-I Human chr17 + 5026563 5026563 5026563 GTTGAGTCCAGGAGTTCGAGACCAGCCTGGGCAACATAGTGAAACCCTGTATCTACAAAACATAG GTTGAGTCCAGGAGTTCGAGACCAGCCTGGGCTACATAGTGAAACCCTGTATCTACAAAACATAG A T KIF1C Ensembl:ENSG00000129250 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1035812979 Functional Loss SNV dbSNP153 33..33 33 - - - 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 46021 RMVar_ID_46021 Human_SNP_ID_615763077 A-to-I Human chr17 + 5026814 5026814 5026814 AGTCAGTCTTTAATAATGTGCACGGGCCAGGCACAGTGGCTCACACCCGTAATCCCAACACTTTG AGTCAGTCTTTAATAATGTGCACGGGCCAGGCTCAGTGGCTCACACCCGTAATCCCAACACTTTG A T KIF1C Ensembl:ENSG00000129250 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1327270017 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8456967 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 46022 RMVar_ID_46022 Human_SNP_ID_615763079 A-to-I Human chr17 + 5026816 5026816 5026816 TCAGTCTTTAATAATGTGCACGGGCCAGGCACAGTGGCTCACACCCGTAATCCCAACACTTTGGA TCAGTCTTTAATAATGTGCACGGGCCAGGCACGGTGGCTCACACCCGTAATCCCAACACTTTGGA A G KIF1C Ensembl:ENSG00000129250 Protein coding 3'UTR GSE38233;GSE100210;GSE99789;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,29796672,31158229 RNA-Seq:(High) rs912442335 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8456967 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 46023 RMVar_ID_46023 Human_SNP_ID_615763094 A-to-I Human chr17 + 5026878 5026878 5026878 GGAATATTAGGGTGGGAGCATCACTTGAGGCCAGGAATTTGAGACCAGCCTGGGCAACATAGTGA GGAATATTAGGGTGGGAGCATCACTTGAGGCCGGGAATTTGAGACCAGCCTGGGCAACATAGTGA A G KIF1C Ensembl:ENSG00000129250 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1035823788 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_493850 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 46024 RMVar_ID_46024 Human_SNP_ID_615763169 A-to-I Human chr17 + 5027126 5027126 5027126 TTCAGATGGGAAGACTGAGGTTTTGTTTATTTATTTTTATTTATTTATTTTTTGAGACGGAGTCT TTCAGATGGGAAGACTGAGGTTTTGTTTATTTTTTTTTATTTATTTATTTTTTGAGACGGAGTCT A T KIF1C Ensembl:ENSG00000129250 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1339584638 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6613508,Human_RBP_ID_23735088 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 46025 RMVar_ID_46025 Human_SNP_ID_615763213 A-to-I Human chr17 + 5027262 5027262 5027262 GCGATTCTCCTGCCTCAGCCTCCTGAGTAGCTAGGATTACAGGCGCCCACAACCGCACCCGGCTA GCGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCGCCCACAACCGCACCCGGCTA A G KIF1C Ensembl:ENSG00000129250 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs917027554 Functional Loss SNV dbSNP153 33..33 33 - - - 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 46026 RMVar_ID_46026 Human_SNP_ID_615763258 A-to-I Human chr17 + 5027392 5027392 5027392 CCTCAGGTGATCCACCCGCCTCTGCCTCCCAAAATGTTGGGATTACAGGCGTGAGCCACCACGCC CCTCAGGTGATCCACCCGCCTCTGCCTCCCAAGATGTTGGGATTACAGGCGTGAGCCACCACGCC A G KIF1C Ensembl:ENSG00000129250 Protein coding 3'UTR GSE47997;GSE38233;GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;cultured B-cells;cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,24183664,24183664,31158229,31158229,31158229 RNA-Seq:(High) rs1173673561 Functional Loss SNV dbSNP153 33..33 33 - - - 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 46027 RMVar_ID_46027 Human_SNP_ID_615763276 A-to-I Human chr17 + 5027456 5027456 5027456 CCAGCCTATTTATTTATTTTTTTAGAATCAAGATCTTGCTATGTTGCCCAGGCTGAACTCGAACT CCAGCCTATTTATTTATTTTTTTAGAATCAAGGTCTTGCTATGTTGCCCAGGCTGAACTCGAACT A G KIF1C Ensembl:ENSG00000129250 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1434863950 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4438992,Human_RBP_ID_23170606 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 46028 RMVar_ID_46028 Human_SNP_ID_615785815 A-to-I Human chr17 - 5107266 5107266 5107266 CTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCGCCCGCCATCATGCTCGGCTAATTTTC CTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTGCAGGCGCCCGCCATCATGCTCGGCTAATTTTC T C ZNF232 Ensembl:ENSG00000167840 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1408193151 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_133959 46029 RMVar_ID_46029 Human_SNP_ID_615785968 A-to-I Human chr17 - 5107810 5107810 5107810 ATGATCTTGGCTGGGCACGGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCTAAGGCAGGT ATGATCTTGGCTGGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTAAGGCAGGT T C ZNF232 Ensembl:ENSG00000167840 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1168999245 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13075203 46030 RMVar_ID_46030 Human_SNP_ID_615808024 A-to-I Human chr17 - 5190197 5190197 5190197 CGCCCAGCTAATTTTGTATTTTTAGTAGACACAGGATTTCTCTCCATGTTGGTCAGGCTGGTCTC CGCCCAGCTAATTTTGTATTTTTAGTAGACACGGGATTTCTCTCCATGTTGGTCAGGCTGGTCTC T C ZNF594 Ensembl:ENSG00000180626 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs914684960 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6614159 46031 RMVar_ID_46031 Human_SNP_ID_615812528 A-to-I Human chr17 - 5207687 5207687 5207687 CCTAGCCAAGATGGTGAAACCCCGTCTCTACTAAAAATACAAAACGCAGCCGGGTGTGGTGGCAC CCTAGCCAAGATGGTGAAACCCCGTCTCTACTTAAAATACAAAACGCAGCCGGGTGTGGTGGCAC T A - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1449800644 Functional Loss SNV dbSNP153 33..33 33 - - - 46032 RMVar_ID_46032 Human_SNP_ID_615812686 A-to-I Human chr17 - 5208436 5208436 5208436 TTGCCTCAGCCTCCCAAAGTGCTGGGATTACAAGTGTGAGCCACCACGCCCAGCTGCCCCCTCTA TTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCACGCCCAGCTGCCCCCTCTA T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs907281782 Functional Loss SNV dbSNP153 33..33 33 - - - 46033 RMVar_ID_46033 Human_SNP_ID_615813995 A-to-I Human chr17 - 5213387 5213386 5213387 ACAAAAATTAGCCAGCGTGATGGTGCACACTTATAGTCCCAGCTACTTGGAAGGCTGAGGTGGGG ACAAAAATTAGCCAGCGTGATGGTGCACACTT_TAGTCCCAGCTACTTGGAAGGCTGAGGTGGGG AT A SCIMP Ensembl:ENSG00000161929 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1567837376 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_181596,RMVar_hsa_circ_104947 46034 RMVar_ID_46034 Human_SNP_ID_615814037 A-to-I Human chr17 - 5213590 5213590 5213590 CACCCGCCTCGACCTCCCAAGGTGCTGGGATTACAGGCATGAGCCACCACACACAGCCAGCATCC CACCCGCCTCGACCTCCCAAGGTGCTGGGATTGCAGGCATGAGCCACCACACACAGCCAGCATCC T C SCIMP Ensembl:ENSG00000161929 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1264580563 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181596,RMVar_hsa_circ_104947 46035 RMVar_ID_46035 Human_SNP_ID_615814058 A-to-I Human chr17 - 5213662 5213662 5213662 TTGTATGTTTAGTAGAGACGGGGTTTCACCATATTGACCAGGCTCGTCTTGAACTCCTGACCTCA TTGTATGTTTAGTAGAGACGGGGTTTCACCATGTTGACCAGGCTCGTCTTGAACTCCTGACCTCA T C SCIMP Ensembl:ENSG00000161929 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1244466026 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181596,RMVar_hsa_circ_104947 46036 RMVar_ID_46036 Human_SNP_ID_615817745 A-to-I Human chr17 + 5227194 5227194 5227194 CGAGTGCAGTAGCTCATGCTTGTAATCCTAGCACTTCAGGAGGCCAAGGCAGGCGGATCACTTGA CGAGTGCAGTAGCTCATGCTTGTAATCCTAGCGCTTCAGGAGGCCAAGGCAGGCGGATCACTTGA A G AC087500.1 Ensembl:ENSG00000261879 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs925385076 Functional Loss SNV dbSNP153 33..33 33 - - - 46037 RMVar_ID_46037 Human_SNP_ID_615818484 A-to-I Human chr17 + 5229598 5229598 5229598 ATATTTTTAGTAGAGATGGCGTTTCACACCATATTGGTCAGGCTGGTCTTGAACTCCTGACTTCA ATATTTTTAGTAGAGATGGCGTTTCACACCATGTTGGTCAGGCTGGTCTTGAACTCCTGACTTCA A G AC087500.1 Ensembl:ENSG00000261879 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1455067806 Functional Loss SNV dbSNP153 33..33 33 - - - 46038 RMVar_ID_46038 Human_SNP_ID_615818623 A-to-I Human chr17 + 5230079 5230079 5230079 CAAACTCTGGGCCCCAAGTGATCCTCCGCCCCAGCCTCCCAAAGTACCAGGATTACAGGCATGAG CAAACTCTGGGCCCCAAGTGATCCTCCGCCCCGGCCTCCCAAAGTACCAGGATTACAGGCATGAG A G AC087500.1 Ensembl:ENSG00000261879 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs577545806 Functional Loss SNV dbSNP153 33..33 33 - - - 46039 RMVar_ID_46039 Human_SNP_ID_615818624 A-to-I Human chr17 + 5230079 5230079 5230079 CAAACTCTGGGCCCCAAGTGATCCTCCGCCCCAGCCTCCCAAAGTACCAGGATTACAGGCATGAG CAAACTCTGGGCCCCAAGTGATCCTCCGCCCCTGCCTCCCAAAGTACCAGGATTACAGGCATGAG A T AC087500.1 Ensembl:ENSG00000261879 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs577545806 Functional Loss SNV dbSNP153 33..33 33 - - - 46040 RMVar_ID_46040 Human_SNP_ID_615818763 A-to-I Human chr17 + 5230659 5230659 5230659 AACCTATATAGCTACTGGGGGCAGTGGCTCACACTTGTAATCCCAGCACTTTGGGAGGCCGAGGC AACCTATATAGCTACTGGGGGCAGTGGCTCACGCTTGTAATCCCAGCACTTTGGGAGGCCGAGGC A G AC087500.1 Ensembl:ENSG00000261879 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1209114758 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5248092 46041 RMVar_ID_46041 Human_SNP_ID_615834999 A-to-I Human chr17 + 5288803 5288803 5288803 TCTGCTCACTGTAACCTCTGCCTCCCAGGTTCAGGCGATTCTCGTGCCTCAGCCCCTCAAGTAGC TCTGCTCACTGTAACCTCTGCCTCCCAGGTTCCGGCGATTCTCGTGCCTCAGCCCCTCAAGTAGC A C RABEP1 Ensembl:ENSG00000029725 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1459608996 Functional Loss SNV dbSNP153 33..33 33 - - - 46042 RMVar_ID_46042 Human_SNP_ID_615836175 A-to-I Human chr17 + 5293140 5293140 5293140 GAAACCCCGTCTCTACTAAACATACAAAAATTAGCTGGGTGTGGTGGTGCGTGCCTGTAATCCCA GAAACCCCGTCTCTACTAAACATACAAAAATTCGCTGGGTGTGGTGGTGCGTGCCTGTAATCCCA A C RABEP1 Ensembl:ENSG00000029725 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1234468934 Functional Loss SNV dbSNP153 33..33 33 - - - 46043 RMVar_ID_46043 Human_SNP_ID_615838982 A-to-I Human chr17 + 5303241 5303241 5303241 GATATACCTACCATACTTAATAGTTTTATTTTATTTTATTTTATTTTTTTTGAGATAGGATCTCA GATATACCTACCATACTTAATAGTTTTATTTTGTTTTATTTTATTTTTTTTGAGATAGGATCTCA A G RABEP1 Ensembl:ENSG00000029725 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1235923744 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181603,RMVar_hsa_circ_181601,RMVar_hsa_circ_181602 46044 RMVar_ID_46044 Human_SNP_ID_615839032 A-to-I Human chr17 + 5303431 5303431 5303431 GTCCGTCTAATTTTTGTATTTTTGGTAGAGACAGGGTTTCGCCACATTGACCAGGTTGGTCTTGA GTCCGTCTAATTTTTGTATTTTTGGTAGAGACGGGGTTTCGCCACATTGACCAGGTTGGTCTTGA A G RABEP1 Ensembl:ENSG00000029725 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1356544409 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181603,RMVar_hsa_circ_181601,RMVar_hsa_circ_181602 46045 RMVar_ID_46045 Human_SNP_ID_615841135 A-to-I Human chr17 + 5311441 5311441 5311441 AAATAAGGCCAGGCACGGTGGCTGACACCTGTAATCCCAGCATTTTGGGAGGCCGAGGCAGGCGG AAATAAGGCCAGGCACGGTGGCTGACACCTGTGATCCCAGCATTTTGGGAGGCCGAGGCAGGCGG A G RABEP1 Ensembl:ENSG00000029725 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs147378939 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181603,RMVar_hsa_circ_181601,RMVar_hsa_circ_181605,RMVar_hsa_circ_292747,RMVar_hsa_circ_181602,RMVar_hsa_circ_348667,RMVar_hsa_circ_308780,RMVar_hsa_circ_181607,RMVar_hsa_circ_271255,RMVar_hsa_circ_181606 46046 RMVar_ID_46046 Human_SNP_ID_615841472 A-to-I Human chr17 + 5312425 5312425 5312425 TGCCCGCCTCAGCCTCCCAAACTGCTGGGATTACAGGCATGAGCCACCGTGCCTGGCCTCATAGA TGCCCGCCTCAGCCTCCCAAACTGCTGGGATTCCAGGCATGAGCCACCGTGCCTGGCCTCATAGA A C RABEP1 Ensembl:ENSG00000029725 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1161580972 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181603,RMVar_hsa_circ_181601,RMVar_hsa_circ_181605,RMVar_hsa_circ_292747,RMVar_hsa_circ_181602,RMVar_hsa_circ_348667,RMVar_hsa_circ_308780,RMVar_hsa_circ_181607,RMVar_hsa_circ_271255,RMVar_hsa_circ_181606 46047 RMVar_ID_46047 Human_SNP_ID_615842591 A-to-I Human chr17 + 5316744 5316741 5316744 AATCCCACCTACTCGGGAGGCTGAGGTAGGAGAATTGCCTGAACCCAAGAGACAGAGTTTGCAGT AATCCCACCTACTCGGGAGGCTGAGGTAGG___ATTGCCTGAACCCAAGAGACAGAGTTTGCAGT GAGA G RABEP1 Ensembl:ENSG00000029725 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1474199001 Functional Loss DEL dbSNP153 31..33 33 - - - RMVar_hsa_circ_181603,RMVar_hsa_circ_181601,RMVar_hsa_circ_181605,RMVar_hsa_circ_292747,RMVar_hsa_circ_181602,RMVar_hsa_circ_348667,RMVar_hsa_circ_308780,RMVar_hsa_circ_181607,RMVar_hsa_circ_271255,RMVar_hsa_circ_181606 46048 RMVar_ID_46048 Human_SNP_ID_615849988 A-to-I Human chr17 + 5343699 5343699 5343699 TCTCTTTTTTTTTTTTTTTTTTTTTTTGAGTCAGGGTCTTGCTGTGTTGCCTAGGCTGGAGTGTA TCTCTTTTTTTTTTTTTTTTTTTTTTTGAGTCCGGGTCTTGCTGTGTTGCCTAGGCTGGAGTGTA A C RABEP1 Ensembl:ENSG00000029725 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1312212063 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1326,RMVar_hsa_circ_3063,RMVar_hsa_circ_181603,RMVar_hsa_circ_292747,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_126806,RMVar_hsa_circ_306081,RMVar_hsa_circ_6632,RMVar_hsa_circ_72658,RMVar_hsa_circ_302419,RMVar_hsa_circ_345775,RMVar_hsa_circ_361589,RMVar_hsa_circ_294488,RMVar_hsa_circ_30225 46049 RMVar_ID_46049 Human_SNP_ID_615849989 A-to-I Human chr17 + 5343699 5343699 5343699 TCTCTTTTTTTTTTTTTTTTTTTTTTTGAGTCAGGGTCTTGCTGTGTTGCCTAGGCTGGAGTGTA TCTCTTTTTTTTTTTTTTTTTTTTTTTGAGTCGGGGTCTTGCTGTGTTGCCTAGGCTGGAGTGTA A G RABEP1 Ensembl:ENSG00000029725 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1312212063 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1326,RMVar_hsa_circ_3063,RMVar_hsa_circ_181603,RMVar_hsa_circ_292747,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_126806,RMVar_hsa_circ_306081,RMVar_hsa_circ_6632,RMVar_hsa_circ_72658,RMVar_hsa_circ_302419,RMVar_hsa_circ_345775,RMVar_hsa_circ_361589,RMVar_hsa_circ_294488,RMVar_hsa_circ_30225 46050 RMVar_ID_46050 Human_SNP_ID_615850063 A-to-I Human chr17 + 5343950 5343950 5343950 CACTCACCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGTCACTGTGCCTGGCCCAAGGTT CACTCACCTTGGCCTCCCAAAGTGCTGGGATTTCAGGCATGAGTCACTGTGCCTGGCCCAAGGTT A T RABEP1 Ensembl:ENSG00000029725 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1045432005 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1326,RMVar_hsa_circ_3063,RMVar_hsa_circ_181603,RMVar_hsa_circ_292747,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_126806,RMVar_hsa_circ_306081,RMVar_hsa_circ_6632,RMVar_hsa_circ_72658,RMVar_hsa_circ_302419,RMVar_hsa_circ_345775,RMVar_hsa_circ_361589,RMVar_hsa_circ_294488,RMVar_hsa_circ_30225 46051 RMVar_ID_46051 Human_SNP_ID_615850157 A-to-I Human chr17 + 5344353 5344353 5344353 CCAGCTACTTGGGAGGCTGAGGCACAAGAATTACTTGAACCCGGGAGATGGAGGCTGCAGTGAGC CCAGCTACTTGGGAGGCTGAGGCACAAGAATTTCTTGAACCCGGGAGATGGAGGCTGCAGTGAGC A T RABEP1 Ensembl:ENSG00000029725 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1460987026 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1326,RMVar_hsa_circ_3063,RMVar_hsa_circ_181603,RMVar_hsa_circ_292747,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_126806,RMVar_hsa_circ_306081,RMVar_hsa_circ_6632,RMVar_hsa_circ_72658,RMVar_hsa_circ_302419,RMVar_hsa_circ_345775,RMVar_hsa_circ_361589,RMVar_hsa_circ_294488,RMVar_hsa_circ_30225 46052 RMVar_ID_46052 Human_SNP_ID_615850905 A-to-I Human chr17 + 5347152 5347152 5347152 CACAAGGTGGCTGGGTACAGTGGCTCACTCCTATAATCCCAGCACTTTGGGAGGCCAAGGTGGGC CACAAGGTGGCTGGGTACAGTGGCTCACTCCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGC A G RABEP1 Ensembl:ENSG00000029725 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1339778971 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1326,RMVar_hsa_circ_3063,RMVar_hsa_circ_181603,RMVar_hsa_circ_348667,RMVar_hsa_circ_308780,RMVar_hsa_circ_181607,RMVar_hsa_circ_78581,RMVar_hsa_circ_369048,RMVar_hsa_circ_74920,RMVar_hsa_circ_181611,RMVar_hsa_circ_181608,RMVar_hsa_circ_126806,RMVar_hsa_circ_306081,RMVar_hsa_circ_6632,RMVar_hsa_circ_72658,RMVar_hsa_circ_345775,RMVar_hsa_circ_361589,RMVar_hsa_circ_294488,RMVar_hsa_circ_30225,RMVar_hsa_circ_181614,RMVar_hsa_circ_73314,RMVar_hsa_circ_276094,RMVar_hsa_circ_307981,RMVar_hsa_circ_341427,RMVar_hsa_circ_333756,RMVar_hsa_circ_294663,RMVar_hsa_circ_276069,RMVar_hsa_circ_10897,RMVar_hsa_circ_53460,RMVar_hsa_circ_181616,RMVar_hsa_circ_181617,RMVar_hsa_circ_181615,RMVar_hsa_circ_181618,RMVar_hsa_circ_181613 46053 RMVar_ID_46053 Human_SNP_ID_615853657 A-to-I Human chr17 + 5358531 5358531 5358531 ATCCCTACTAAAAATACAAAAATTAGTCGTGCATGGTGTCTGGCGCCTGTCGTCCCAGCTACTCA ATCCCTACTAAAAATACAAAAATTAGTCGTGCGTGGTGTCTGGCGCCTGTCGTCCCAGCTACTCA A G RABEP1 Ensembl:ENSG00000029725 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1307941453 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1326,RMVar_hsa_circ_3063,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_361589,RMVar_hsa_circ_294488,RMVar_hsa_circ_73314,RMVar_hsa_circ_276094,RMVar_hsa_circ_307981,RMVar_hsa_circ_341427,RMVar_hsa_circ_294663,RMVar_hsa_circ_10897,RMVar_hsa_circ_53460,RMVar_hsa_circ_181616,RMVar_hsa_circ_181617,RMVar_hsa_circ_181615,RMVar_hsa_circ_72700,RMVar_hsa_circ_105668,RMVar_hsa_circ_331716,RMVar_hsa_circ_335011,RMVar_hsa_circ_311396,RMVar_hsa_circ_87178,RMVar_hsa_circ_181620,RMVar_hsa_circ_181621,RMVar_hsa_circ_181622,RMVar_hsa_circ_181619,RMVar_hsa_circ_181624,RMVar_hsa_circ_286348,RMVar_hsa_circ_310211,RMVar_hsa_circ_355715,RMVar_hsa_circ_328520,RMVar_hsa_circ_301614,RMVar_hsa_circ_181626,RMVar_hsa_circ_181627,RMVar_hsa_circ_181625 46054 RMVar_ID_46054 Human_SNP_ID_615860903 A-to-I Human chr17 + 5382342 5382332 5382343 GACCTCAGGTGATCCACCTGCCTCAGCCTCCCAAATTGCTGGGATTACAGGCGTGAGCCACCGTG GACCTCAGGTGATCCACCTGCCT___________ATTGCTGGGATTACAGGCGTGAGCCACCGTG TCAGCCTCCCAA T RABEP1 Ensembl:ENSG00000029725 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs991462377 Functional Loss DEL dbSNP153 24..34 33 - - - 46055 RMVar_ID_46055 Human_SNP_ID_615860949 A-to-I Human chr17 + 5382491 5382491 5382491 CTAGTCTGGGCCAGGCATGGTGGCTCACGCCTATAATCCCAGCAGTATGGGAGGCTGACATGGAT CTAGTCTGGGCCAGGCATGGTGGCTCACGCCTGTAATCCCAGCAGTATGGGAGGCTGACATGGAT A G RABEP1 Ensembl:ENSG00000029725 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1012534801 Functional Loss SNV dbSNP153 33..33 33 - - - 46056 RMVar_ID_46056 Human_SNP_ID_615860978 A-to-I Human chr17 + 5382596 5382596 5382596 CAATATGGTGAAACCCCGTCTCTACTTAAAATACAAAAATTAGCCGGGCATGGTGGCGTGTGCTT CAATATGGTGAAACCCCGTCTCTACTTAAAATGCAAAAATTAGCCGGGCATGGTGGCGTGTGCTT A G RABEP1 Ensembl:ENSG00000029725 Protein coding intron GSE47997;GSE38233;GSE38233 K562 cells&HepG2 cells;cultured B-cells;cultured B-cells - 23474544,24183664,24183664 RNA-Seq:(High) rs1019087509 Functional Loss SNV dbSNP153 33..33 33 - - - 46057 RMVar_ID_46057 Human_SNP_ID_615860992 A-to-I Human chr17 + 5382629 5382629 5382629 CAAAAATTAGCCGGGCATGGTGGCGTGTGCTTATAATCCCAGCTACTTGGGAGGCTGAGACAGGA CAAAAATTAGCCGGGCATGGTGGCGTGTGCTTTTAATCCCAGCTACTTGGGAGGCTGAGACAGGA A T RABEP1 Ensembl:ENSG00000029725 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1228223307 Functional Loss SNV dbSNP153 33..33 33 - - - 46058 RMVar_ID_46058 Human_SNP_ID_615861054 A-to-I Human chr17 + 5382859 5382858 5382860 GGAGAATCACTTGAACCCGGGAGGTGGAGACTACAGTGAGCCGAGATCACACCATTGCACTCTGG GGAGAATCACTTGAACCCGGGAGGTGGAGACT__AGTGAGCCGAGATCACACCATTGCACTCTGG TAC T RABEP1 Ensembl:ENSG00000029725 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1346424439 Functional Loss DEL dbSNP153 33..34 33 - - - 46059 RMVar_ID_46059 Human_SNP_ID_615861062 A-to-I Human chr17 + 5382875 5382875 5382875 CCGGGAGGTGGAGACTACAGTGAGCCGAGATCACACCATTGCACTCTGGCCTGGGCTGGCCTGGA CCGGGAGGTGGAGACTACAGTGAGCCGAGATCTCACCATTGCACTCTGGCCTGGGCTGGCCTGGA A T RABEP1 Ensembl:ENSG00000029725 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1164530890 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13077506 46060 RMVar_ID_46060 Human_SNP_ID_615861064 A-to-I Human chr17 - 5382881 5382881 5382881 TCATCATCCAGGCCAGCCCAGGCCAGAGTGCAATGGTGTGATCTCGGCTCACTGTAGTCTCCACC TCATCATCCAGGCCAGCCCAGGCCAGAGTGCATTGGTGTGATCTCGGCTCACTGTAGTCTCCACC T A NUP88 Ensembl:ENSG00000108559 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1056166532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13077505,Human_RBP_ID_22475531 46061 RMVar_ID_46061 Human_SNP_ID_615861065 A-to-I Human chr17 - 5382881 5382881 5382881 TCATCATCCAGGCCAGCCCAGGCCAGAGTGCAATGGTGTGATCTCGGCTCACTGTAGTCTCCACC TCATCATCCAGGCCAGCCCAGGCCAGAGTGCAGTGGTGTGATCTCGGCTCACTGTAGTCTCCACC T C NUP88 Ensembl:ENSG00000108559 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1056166532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13077505,Human_RBP_ID_22475531 46062 RMVar_ID_46062 Human_SNP_ID_615862933 A-to-I Human chr17 - 5388567 5388567 5388567 GAAGTTAGGCTAGGCCGGGCGTGGTGGCTCACACCTGTAATCTCAGCACTTTGGGAGACCAAGAC GAAGTTAGGCTAGGCCGGGCGTGGTGGCTCACGCCTGTAATCTCAGCACTTTGGGAGACCAAGAC T C NUP88 Ensembl:ENSG00000108559 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1196765764 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81020,RMVar_hsa_circ_85277,RMVar_hsa_circ_8958,RMVar_hsa_circ_181643,RMVar_hsa_circ_181644,RMVar_hsa_circ_103669,RMVar_hsa_circ_89124,RMVar_hsa_circ_181645,RMVar_hsa_circ_181646 46063 RMVar_ID_46063 Human_SNP_ID_615863598 A-to-I Human chr17 - 5390855 5390855 5390855 CCCCATCTCTACAAAAAACAAAAAAATTAGCCAGGCATGGTGGTACACATCTGTAGTCCTAGCTG CCCCATCTCTACAAAAAACAAAAAAATTAGCCGGGCATGGTGGTACACATCTGTAGTCCTAGCTG T C NUP88 Ensembl:ENSG00000108559 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs890115361 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_573,RMVar_hsa_circ_81020,RMVar_hsa_circ_85277,RMVar_hsa_circ_8958,RMVar_hsa_circ_181643,RMVar_hsa_circ_181644,RMVar_hsa_circ_103669,RMVar_hsa_circ_89124,RMVar_hsa_circ_181645,RMVar_hsa_circ_302681,RMVar_hsa_circ_312650,RMVar_hsa_circ_181646,RMVar_hsa_circ_311252,RMVar_hsa_circ_125011,RMVar_hsa_circ_181648,RMVar_hsa_circ_181649,RMVar_hsa_circ_181647 46064 RMVar_ID_46064 Human_SNP_ID_615865008 A-to-I Human chr17 - 5396028 5396028 5396028 TTTTGTGTTTTTAGTAGAGACGGCGTCTCGCTATGTTGGCCAGGCTGGTCTTGAACTCCTGACCT TTTTGTGTTTTTAGTAGAGACGGCGTCTCGCTGTGTTGGCCAGGCTGGTCTTGAACTCCTGACCT T C NUP88 Ensembl:ENSG00000108559 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs376650958 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_573,RMVar_hsa_circ_81020,RMVar_hsa_circ_8958,RMVar_hsa_circ_181644,RMVar_hsa_circ_103669,RMVar_hsa_circ_89124,RMVar_hsa_circ_181645,RMVar_hsa_circ_302681,RMVar_hsa_circ_312650,RMVar_hsa_circ_181646,RMVar_hsa_circ_311252,RMVar_hsa_circ_181651,RMVar_hsa_circ_181648,RMVar_hsa_circ_294637,RMVar_hsa_circ_181647,RMVar_hsa_circ_269682,RMVar_hsa_circ_70125,RMVar_hsa_circ_181652,RMVar_hsa_circ_181654,RMVar_hsa_circ_336277,RMVar_hsa_circ_292639,RMVar_hsa_circ_181653 46065 RMVar_ID_46065 Human_SNP_ID_615870122 A-to-I Human chr17 - 5415136 5415136 5415136 ACACGCCTGTAGTCCCAGCTACTCAGGAGGTTAAGGCACAAGTATTGATTAAATCCAGGAGGCGG ACACGCCTGTAGTCCCAGCTACTCAGGAGGTTGAGGCACAAGTATTGATTAAATCCAGGAGGCGG T C NUP88 Ensembl:ENSG00000108559 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs974534391 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_311252,RMVar_hsa_circ_70125,RMVar_hsa_circ_181652,RMVar_hsa_circ_282297,RMVar_hsa_circ_181657,RMVar_hsa_circ_181658,RMVar_hsa_circ_293496,RMVar_hsa_circ_290398,RMVar_hsa_circ_181660,RMVar_hsa_circ_181663,RMVar_hsa_circ_295406,RMVar_hsa_circ_110625,RMVar_hsa_circ_181665 46066 RMVar_ID_46066 Human_SNP_ID_615871158 A-to-I Human chr17 - 5418284 5418284 5418284 ACGCCCCTGCACTACAGCCTGGGCAACAGAGCAAGACTGTGTCTCAAAAAATAATAATAATTACC ACGCCCCTGCACTACAGCCTGGGCAACAGAGCGAGACTGTGTCTCAAAAAATAATAATAATTACC T C NUP88 Ensembl:ENSG00000108559 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1359756422 Functional Loss SNV dbSNP153 33..33 33 - - - 46067 RMVar_ID_46067 Human_SNP_ID_615872833 A-to-I Human chr17 + 5423783 5423783 5423783 TGTTTGGTTTTTGTTTTTGTTTTTTTTGAGACAGGGTCTCTGCCCAGGCTGGAATGCAGTGGCGT TGTTTGGTTTTTGTTTTTGTTTTTTTTGAGACGGGGTCTCTGCCCAGGCTGGAATGCAGTGGCGT A G RPAIN Ensembl:ENSG00000129197 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1275253139 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_237772,Human_RBP_ID_768428,Human_RBP_ID_6615804,Human_RBP_ID_13080545 RMVar_hsa_circ_52332,RMVar_hsa_circ_181666 46068 RMVar_ID_46068 Human_SNP_ID_615873005 A-to-I Human chr17 + 5424331 5424331 5424331 TTTAAATTTTTTTGTAGAGGCAGGGTCTCACTATGTTGCCTAGGCTGGTCTCAAACAGCTGGACT TTTAAATTTTTTTGTAGAGGCAGGGTCTCACTTTGTTGCCTAGGCTGGTCTCAAACAGCTGGACT A T RPAIN Ensembl:ENSG00000129197 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1020791349 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13080565 RMVar_hsa_circ_52332,RMVar_hsa_circ_181666 46069 RMVar_ID_46069 Human_SNP_ID_615873014 A-to-I Human chr17 + 5424370 5424370 5424370 CTAGGCTGGTCTCAAACAGCTGGACTCAAACCATCCTCCTACTTCAGCCTCCCAAAGTGTTGGGA CTAGGCTGGTCTCAAACAGCTGGACTCAAACCGTCCTCCTACTTCAGCCTCCCAAAGTGTTGGGA A G RPAIN Ensembl:ENSG00000129197 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs962210787 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13080565 RMVar_hsa_circ_52332,RMVar_hsa_circ_181666 46070 RMVar_ID_46070 Human_SNP_ID_615873635 A-to-I Human chr17 + 5426740 5426738 5426741 TAGGCTCACTGCAACCTCTGCCTTGCGGGTTCAAGTCATTCTCCTGCCTCAGCCTCCCAAGTAGC TAGGCTCACTGCAACCTCTGCCTTGCGGGTT___GTCATTCTCCTGCCTCAGCCTCCCAAGTAGC TCAA T RPAIN Ensembl:ENSG00000129197 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1555531762 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_8457345,Human_RBP_ID_13080701 RMVar_hsa_circ_6190 46071 RMVar_ID_46071 Human_SNP_ID_615873636 A-to-I Human chr17 + 5426740 5426739 5426741 TAGGCTCACTGCAACCTCTGCCTTGCGGGTTCAAGTCATTCTCCTGCCTCAGCCTCCCAAGTAGC TAGGCTCACTGCAACCTCTGCCTTGCGGGTTC__GTCATTCTCCTGCCTCAGCCTCCCAAGTAGC CAA C RPAIN Ensembl:ENSG00000129197 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs80354551 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_8457345,Human_RBP_ID_13080701 RMVar_hsa_circ_6190 46072 RMVar_ID_46072 Human_SNP_ID_615873771 A-to-I Human chr17 + 5427275 5427275 5427275 CTCCTGCCTCAGCCTCTTGAGTAGCTGGGATTACAGGCACGTGCCACCATGCCTGGCTAATTTTT CTCCTGCCTCAGCCTCTTGAGTAGCTGGGATTTCAGGCACGTGCCACCATGCCTGGCTAATTTTT A T RPAIN Ensembl:ENSG00000129197 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1354584074 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6190 46073 RMVar_ID_46073 Human_SNP_ID_615875355 A-to-I Human chr17 + 5432793 5432793 5432793 AAAAAGACAAACTGCCTTGGAGGAGATAAACCAATTTTATGTCTATCATGTTATACAAAAATCTA AAAAAGACAAACTGCCTTGGAGGAGATAAACCGATTTTATGTCTATCATGTTATACAAAAATCTA A G RPAIN Ensembl:ENSG00000129197 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs533876489 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_494226,Human_RBP_ID_1009297,Human_RBP_ID_1537587,Human_RBP_ID_1863348,Human_RBP_ID_3529106,Human_RBP_ID_6616003,Human_RBP_ID_17896445,Human_RBP_ID_26643789,Human_RBP_ID_27667006 46074 RMVar_ID_46074 Human_SNP_ID_615875362 A-to-I Human chr17 - 5432830 5432830 5432830 TTTATTATCATTTTTTTCTGTACAAATCTATTATTTCTAGATTTTTGTATAACATGATAGACATA TTTATTATCATTTTTTTCTGTACAAATCTATTGTTTCTAGATTTTTGTATAACATGATAGACATA T C AC004148.1,C1QBP Ensembl:ENSG00000263272,Ensembl:ENSG00000108561 lincRNA,Protein coding exon,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978643404 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_494228,Human_RBP_ID_1537589,Human_RBP_ID_1863349,Human_RBP_ID_2513336,Human_RBP_ID_3529107,Human_RBP_ID_6616004,Human_RBP_ID_8947919,Human_RBP_ID_17492443,Human_RBP_ID_17654036,Human_RBP_ID_18702963,Human_RBP_ID_21889717,Human_RBP_ID_22805659,Human_RBP_ID_23209792,Human_RBP_ID_24371635,Human_RBP_ID_24415551,Human_RBP_ID_24479822,Human_RBP_ID_26460749,Human_RBP_ID_26643790,Human_RBP_ID_26811859,Human_RBP_ID_26966650,Human_RBP_ID_27257008 Human_miRNA_ID_1086210 RMVar_hsa_circ_120727,RMVar_hsa_circ_181667,RMVar_hsa_circ_181668 46075 RMVar_ID_46075 Human_SNP_ID_615876721 A-to-I Human chr17 - 5436855 5436855 5436855 CAGGCGTGCGTCCGGTTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCGTGTTGGCCAGGC CAGGCGTGCGTCCGGTTAATTTTTGTATTTTTCGTAGAGACAGGGTTTCACCGTGTTGGCCAGGC T G C1QBP Ensembl:ENSG00000108561 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs565164324 Functional Loss SNV dbSNP153 33..33 33 - - - 46076 RMVar_ID_46076 Human_SNP_ID_615876745 A-to-I Human chr17 - 5436920 5436920 5436920 TCACTGCAACCTCTGCCTCCCAGGTTCTGACAATTCTCCTGCCTCAGCCTCCTTAGCTGGGATTA TCACTGCAACCTCTGCCTCCCAGGTTCTGACAGTTCTCCTGCCTCAGCCTCCTTAGCTGGGATTA T C C1QBP Ensembl:ENSG00000108561 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1340922997 Functional Loss SNV dbSNP153 33..33 33 - - - 46077 RMVar_ID_46077 Human_SNP_ID_615883186 A-to-I Human chr17 - 5461455 5461455 5461455 ACCACCGCACCTGGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGA ACCACCGCACCTGGCTAATTTTTTGTATTTTTGGTAGAGACGGGGTTTCACCGTGTTAGCCAGGA T C DHX33 Ensembl:ENSG00000005100 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs891486337 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181670,RMVar_hsa_circ_79744,RMVar_hsa_circ_315139,RMVar_hsa_circ_35728,RMVar_hsa_circ_181673,RMVar_hsa_circ_288679,RMVar_hsa_circ_338691,RMVar_hsa_circ_181676,RMVar_hsa_circ_181677,RMVar_hsa_circ_356130,RMVar_hsa_circ_311143,RMVar_hsa_circ_109375,RMVar_hsa_circ_181685,RMVar_hsa_circ_181683,RMVar_hsa_circ_181682,RMVar_hsa_circ_373904,RMVar_hsa_circ_272600,RMVar_hsa_circ_286397,RMVar_hsa_circ_181686 46078 RMVar_ID_46078 Human_SNP_ID_615883188 A-to-I Human chr17 - 5461470 5461470 5461470 GGACTACAGGCGCCCACCACCGCACCTGGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCA GGACTACAGGCGCCCACCACCGCACCTGGCTACTTTTTTGTATTTTTAGTAGAGACGGGGTTTCA T G DHX33 Ensembl:ENSG00000005100 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1490726078 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181670,RMVar_hsa_circ_79744,RMVar_hsa_circ_315139,RMVar_hsa_circ_35728,RMVar_hsa_circ_181673,RMVar_hsa_circ_288679,RMVar_hsa_circ_338691,RMVar_hsa_circ_181676,RMVar_hsa_circ_181677,RMVar_hsa_circ_356130,RMVar_hsa_circ_311143,RMVar_hsa_circ_109375,RMVar_hsa_circ_181685,RMVar_hsa_circ_181683,RMVar_hsa_circ_181682,RMVar_hsa_circ_373904,RMVar_hsa_circ_272600,RMVar_hsa_circ_286397,RMVar_hsa_circ_181686 46079 RMVar_ID_46079 Human_SNP_ID_615883189 A-to-I Human chr17 - 5461471 5461471 5461471 GGGACTACAGGCGCCCACCACCGCACCTGGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTC GGGACTACAGGCGCCCACCACCGCACCTGGCTGATTTTTTGTATTTTTAGTAGAGACGGGGTTTC T C DHX33 Ensembl:ENSG00000005100 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs754985768 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181670,RMVar_hsa_circ_79744,RMVar_hsa_circ_315139,RMVar_hsa_circ_35728,RMVar_hsa_circ_181673,RMVar_hsa_circ_288679,RMVar_hsa_circ_338691,RMVar_hsa_circ_181676,RMVar_hsa_circ_181677,RMVar_hsa_circ_356130,RMVar_hsa_circ_311143,RMVar_hsa_circ_109375,RMVar_hsa_circ_181685,RMVar_hsa_circ_181683,RMVar_hsa_circ_181682,RMVar_hsa_circ_373904,RMVar_hsa_circ_272600,RMVar_hsa_circ_286397,RMVar_hsa_circ_181686 46080 RMVar_ID_46080 Human_SNP_ID_615883224 A-to-I Human chr17 - 5461566 5461566 5461566 TTACCCAGGCTGCAGCGTGGTGACGCGATCTCAGCTCACTGCAAGCTCCGCCTCCCAGGTTCACG TTACCCAGGCTGCAGCGTGGTGACGCGATCTCGGCTCACTGCAAGCTCCGCCTCCCAGGTTCACG T C DHX33 Ensembl:ENSG00000005100 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs370878061 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5129433,Human_RBP_ID_13081516,Human_RBP_ID_22475532,Human_RBP_ID_26966707 RMVar_hsa_circ_181670,RMVar_hsa_circ_79744,RMVar_hsa_circ_315139,RMVar_hsa_circ_35728,RMVar_hsa_circ_181673,RMVar_hsa_circ_288679,RMVar_hsa_circ_338691,RMVar_hsa_circ_181676,RMVar_hsa_circ_181677,RMVar_hsa_circ_356130,RMVar_hsa_circ_311143,RMVar_hsa_circ_109375,RMVar_hsa_circ_181685,RMVar_hsa_circ_181683,RMVar_hsa_circ_181682,RMVar_hsa_circ_373904,RMVar_hsa_circ_272600,RMVar_hsa_circ_286397,RMVar_hsa_circ_181686 46081 RMVar_ID_46081 Human_SNP_ID_615883288 A-to-I Human chr17 - 5461753 5461753 5461753 CCTGAGGTCAGGAGATCGAGACCAGCCTGGCCAACGTGGTGAAACCCCGTCTCTACTAAAAATAC CCTGAGGTCAGGAGATCGAGACCAGCCTGGCCCACGTGGTGAAACCCCGTCTCTACTAAAAATAC T G DHX33 Ensembl:ENSG00000005100 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1013887630 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181670,RMVar_hsa_circ_79744,RMVar_hsa_circ_315139,RMVar_hsa_circ_35728,RMVar_hsa_circ_181673,RMVar_hsa_circ_288679,RMVar_hsa_circ_338691,RMVar_hsa_circ_181676,RMVar_hsa_circ_181677,RMVar_hsa_circ_356130,RMVar_hsa_circ_311143,RMVar_hsa_circ_109375,RMVar_hsa_circ_181685,RMVar_hsa_circ_181683,RMVar_hsa_circ_181682,RMVar_hsa_circ_373904,RMVar_hsa_circ_272600,RMVar_hsa_circ_286397,RMVar_hsa_circ_181686 46082 RMVar_ID_46082 Human_SNP_ID_615883313 A-to-I Human chr17 - 5461840 5461840 5461840 TGATCTGAAAGTATCCAGATAATTGGCCCGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTG TGATCTGAAAGTATCCAGATAATTGGCCCGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTG T C DHX33 Ensembl:ENSG00000005100 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1296243825 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13081525 RMVar_hsa_circ_181670,RMVar_hsa_circ_79744,RMVar_hsa_circ_315139,RMVar_hsa_circ_35728,RMVar_hsa_circ_181673,RMVar_hsa_circ_288679,RMVar_hsa_circ_338691,RMVar_hsa_circ_181676,RMVar_hsa_circ_181677,RMVar_hsa_circ_356130,RMVar_hsa_circ_311143,RMVar_hsa_circ_109375,RMVar_hsa_circ_181685,RMVar_hsa_circ_181683,RMVar_hsa_circ_181682,RMVar_hsa_circ_373904,RMVar_hsa_circ_272600,RMVar_hsa_circ_286397,RMVar_hsa_circ_181686 46083 RMVar_ID_46083 Human_SNP_ID_615883384 A-to-I Human chr17 - 5462077 5462077 5462077 AAATTAGCTGGGTGTGGTGGCACACATCTGTAATCCCAGCTACTTGGGTGGCTGAGGCATGAGAA AAATTAGCTGGGTGTGGTGGCACACATCTGTAGTCCCAGCTACTTGGGTGGCTGAGGCATGAGAA T C DHX33 Ensembl:ENSG00000005100 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs757225433 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_130272 RMVar_hsa_circ_181670,RMVar_hsa_circ_79744,RMVar_hsa_circ_315139,RMVar_hsa_circ_35728,RMVar_hsa_circ_181673,RMVar_hsa_circ_288679,RMVar_hsa_circ_338691,RMVar_hsa_circ_181676,RMVar_hsa_circ_181677,RMVar_hsa_circ_356130,RMVar_hsa_circ_311143,RMVar_hsa_circ_109375,RMVar_hsa_circ_181685,RMVar_hsa_circ_181683,RMVar_hsa_circ_181682,RMVar_hsa_circ_373904,RMVar_hsa_circ_272600,RMVar_hsa_circ_286397,RMVar_hsa_circ_181686 46084 RMVar_ID_46084 Human_SNP_ID_615886904 A-to-I Human chr17 - 5475710 5475710 5475710 CAGTCTTGCTCTGTCGCCCAGGCTGGAGTGCAATGGAGCAGTCTCAGCTCACTGTAACCTGTGCC CAGTCTTGCTCTGTCGCCCAGGCTGGAGTGCAGTGGAGCAGTCTCAGCTCACTGTAACCTGTGCC T C DERL2 Ensembl:ENSG00000072849 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1041270738 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181689,RMVar_hsa_circ_104295,RMVar_hsa_circ_181688 46085 RMVar_ID_46085 Human_SNP_ID_615889940 A-to-I Human chr17 + 5487219 5487219 5487219 TTAGGAGGCAGAGGTTGTAGCGAGCCGAGATCATACCACTGTACTCCAGCCTGGGCGAAAGAGTG TTAGGAGGCAGAGGTTGTAGCGAGCCGAGATCGTACCACTGTACTCCAGCCTGGGCGAAAGAGTG A G MIS12 Ensembl:ENSG00000167842 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs182855813 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25303115 46086 RMVar_ID_46086 Human_SNP_ID_615889971 A-to-I Human chr17 + 5487325 5487325 5487325 AGGCATGGTGGCCTGCACCTGTTGTCCCGGCTACTTGGGAGACTGAGGTGGGAGGATTGCTTGGG AGGCATGGTGGCCTGCACCTGTTGTCCCGGCTGCTTGGGAGACTGAGGTGGGAGGATTGCTTGGG A G MIS12 Ensembl:ENSG00000167842 Protein coding intron GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459,32596459 RNA-Seq:(High) rs1049337523 Functional Loss SNV dbSNP153 33..33 33 - - - 46087 RMVar_ID_46087 Human_SNP_ID_616186172 A-to-I Human chr17 - 6625895 6625895 6625895 GAGTTTGAGACCAGCCTGGCCAACAGGCCAAAACCTTGTCTCTACTAAAGATACAAAAATTAGTT GAGTTTGAGACCAGCCTGGCCAACAGGCCAAACCCTTGTCTCTACTAAAGATACAAAAATTAGTT T G KIAA0753 Ensembl:ENSG00000198920 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1188281113 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2930,RMVar_hsa_circ_344296,RMVar_hsa_circ_321286,RMVar_hsa_circ_11941,RMVar_hsa_circ_118110,RMVar_hsa_circ_100477,RMVar_hsa_circ_181726,RMVar_hsa_circ_181727,RMVar_hsa_circ_11830,RMVar_hsa_circ_314775,RMVar_hsa_circ_181728 46088 RMVar_ID_46088 Human_SNP_ID_616204323 A-to-I Human chr17 - 6695557 6695557 6695557 GTGAAACCCTGTCTCTACTAAAAATACAGAAAATTAGCGAGGCATGGTGGCACATGCCTGTAGTC GTGAAACCCTGTCTCTACTAAAAATACAGAAAGTTAGCGAGGCATGGTGGCACATGCCTGTAGTC T C SLC13A5 Ensembl:ENSG00000141485 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1416264105 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76797,RMVar_hsa_circ_97771,RMVar_hsa_circ_181732,RMVar_hsa_circ_181733,RMVar_hsa_circ_110237,RMVar_hsa_circ_181735,RMVar_hsa_circ_80841,RMVar_hsa_circ_181736 46089 RMVar_ID_46089 Human_SNP_ID_616204324 A-to-I Human chr17 - 6695557 6695557 6695557 GTGAAACCCTGTCTCTACTAAAAATACAGAAAATTAGCGAGGCATGGTGGCACATGCCTGTAGTC GTGAAACCCTGTCTCTACTAAAAATACAGAAACTTAGCGAGGCATGGTGGCACATGCCTGTAGTC T G SLC13A5 Ensembl:ENSG00000141485 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1416264105 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76797,RMVar_hsa_circ_97771,RMVar_hsa_circ_181732,RMVar_hsa_circ_181733,RMVar_hsa_circ_110237,RMVar_hsa_circ_181735,RMVar_hsa_circ_80841,RMVar_hsa_circ_181736 46090 RMVar_ID_46090 Human_SNP_ID_616204325 A-to-I Human chr17 - 6695564 6695564 6695564 CAACATGGTGAAACCCTGTCTCTACTAAAAATACAGAAAATTAGCGAGGCATGGTGGCACATGCC CAACATGGTGAAACCCTGTCTCTACTAAAAATGCAGAAAATTAGCGAGGCATGGTGGCACATGCC T C SLC13A5 Ensembl:ENSG00000141485 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1461018694 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76797,RMVar_hsa_circ_97771,RMVar_hsa_circ_181732,RMVar_hsa_circ_181733,RMVar_hsa_circ_110237,RMVar_hsa_circ_181735,RMVar_hsa_circ_80841,RMVar_hsa_circ_181736 46091 RMVar_ID_46091 Human_SNP_ID_616204327 A-to-I Human chr17 - 6695573 6695573 6695573 CATCCTGGCCAACATGGTGAAACCCTGTCTCTACTAAAAATACAGAAAATTAGCGAGGCATGGTG CATCCTGGCCAACATGGTGAAACCCTGTCTCTTCTAAAAATACAGAAAATTAGCGAGGCATGGTG T A SLC13A5 Ensembl:ENSG00000141485 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1224101707 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76797,RMVar_hsa_circ_97771,RMVar_hsa_circ_181732,RMVar_hsa_circ_181733,RMVar_hsa_circ_110237,RMVar_hsa_circ_181735,RMVar_hsa_circ_80841,RMVar_hsa_circ_181736 46092 RMVar_ID_46092 Human_SNP_ID_616271421 A-to-I Human chr17 - 6968062 6968062 6968062 CAATGGTGTGATCTCAGCTCACTGCAACCTCCACCTCCTGGGTTCAAGCAACTCTCCCGCCTCAG CAATGGTGTGATCTCAGCTCACTGCAACCTCCCCCTCCTGGGTTCAAGCAACTCTCCCGCCTCAG T G AC027763.2,ALOX12-AS1 Ensembl:ENSG00000263316,Ensembl:ENSG00000215067 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs963998064 Functional Loss SNV dbSNP153 33..33 33 - - - 46093 RMVar_ID_46093 Human_SNP_ID_616282746 A-to-I Human chr17 - 7011556 7011556 7011556 CACTCGGGATGGTGAGGCGGGATAATCCCTTGAACCCGGGAGGCGAAGGTTGCAGTGAGCTGAGA CACTCGGGATGGTGAGGCGGGATAATCCCTTGGACCCGGGAGGCGAAGGTTGCAGTGAGCTGAGA T C AC040977.2,ALOX12-AS1 Ensembl:ENSG00000267047,Ensembl:ENSG00000215067 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1463855813 Functional Loss SNV dbSNP153 33..33 33 - - - 46094 RMVar_ID_46094 Human_SNP_ID_616291595 A-to-I Human chr17 + 7040900 7040900 7040900 CTGTGGCTTAGAAAAGAAATTGAGGGCTGGGCATGGTGGCTCACGTCTGTAATCCCAACACTTTG CTGTGGCTTAGAAAAGAAATTGAGGGCTGGGCGTGGTGGCTCACGTCTGTAATCCCAACACTTTG A G - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs921902759 Functional Loss SNV dbSNP153 33..33 33 - - - 46095 RMVar_ID_46095 Human_SNP_ID_616291600 A-to-I Human chr17 + 7040910 7040910 7040910 GAAAAGAAATTGAGGGCTGGGCATGGTGGCTCACGTCTGTAATCCCAACACTTTGGGAGGCCGAG GAAAAGAAATTGAGGGCTGGGCATGGTGGCTCCCGTCTGTAATCCCAACACTTTGGGAGGCCGAG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917258401 Functional Loss SNV dbSNP153 33..33 33 - - - 46096 RMVar_ID_46096 Human_SNP_ID_616344221 A-to-I Human chr17 + 7224226 7224226 7224226 TTTGGGAATGCTGGCCTCCTGCTAGGAGAGGCAGGCAAACAGCTGAGGCGGTAGGCTTAGGGCCA TTTGGGAATGCTGGCCTCCTGCTAGGAGAGGCCGGCAAACAGCTGAGGCGGTAGGCTTAGGGCCA A C ACADVL Ensembl:ENSG00000072778 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) 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 46097 RMVar_ID_46097 Human_SNP_ID_616347743 A-to-I Human chr17 - 7233621 7233620 7233622 ACACGGTGAAACCCCATCTCTACTAACTAAAAATACAAAAAATTAGCCGGGCGTGGGGGCACGCG ACACGGTGAAACCCCATCTCTACTAACTAAA__TACAAAAAATTAGCCGGGCGTGGGGGCACGCG ATT A DVL2 Ensembl:ENSG00000004975 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs369035614 Functional Loss DEL dbSNP153 32..33 33 - - - 46098 RMVar_ID_46098 Human_SNP_ID_616352034 A-to-I Human chr17 - 7245192 7245192 7245192 CGACTTCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATCACAGGCACCTG CGACTTCCAGGTTCAAGCAATTCTCCTGCCTCGGCCTCCCAAGTAGCTGGGATCACAGGCACCTG T C CTDNEP1 Ensembl:ENSG00000175826 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1031383270 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16538,RMVar_hsa_circ_181774,RMVar_hsa_circ_112880,RMVar_hsa_circ_367724,RMVar_hsa_circ_181776 46099 RMVar_ID_46099 Human_SNP_ID_616352077 A-to-I Human chr17 - 7245333 7245333 7245333 CAGCCTCTCAGTAGTTGGGACTACAGGCGTGCACCACCATGCCCAGCTAATTTTTTTATTTTTTA CAGCCTCTCAGTAGTTGGGACTACAGGCGTGCGCCACCATGCCCAGCTAATTTTTTTATTTTTTA T C CTDNEP1 Ensembl:ENSG00000175826 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1048465932 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16538,RMVar_hsa_circ_181774,RMVar_hsa_circ_112880,RMVar_hsa_circ_367724,RMVar_hsa_circ_181776 46100 RMVar_ID_46100 Human_SNP_ID_616352865 A-to-I Human chr17 - 7248006 7248006 7248006 CGCCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGCGCCTGGCTGATTCTA CGCCTGCCTTGGCCTCCCAAAGTGCTGGGATTGCAGGCATGAGCCACTGCGCCTGGCTGATTCTA T C AC003688.2,CTDNEP1 Ensembl:ENSG00000262302,Ensembl:ENSG00000175826 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1057469763 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16538 46101 RMVar_ID_46101 Human_SNP_ID_616376244 A-to-I Human chr17 - 7320317 7320317 7320317 CAGCCTAGGCAATATAGTGAAACTCTGTCTCTACAAAAAAAATACAAAAATTCTCCAGGCATGGT CAGCCTAGGCAATATAGTGAAACTCTGTCTCTGCAAAAAAAATACAAAAATTCTCCAGGCATGGT T C NEURL4 Ensembl:ENSG00000215041 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1291640907 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91827,RMVar_hsa_circ_181803,RMVar_hsa_circ_100727,RMVar_hsa_circ_124773,RMVar_hsa_circ_181805,RMVar_hsa_circ_125462,RMVar_hsa_circ_181806,RMVar_hsa_circ_181807 46102 RMVar_ID_46102 Human_SNP_ID_616381567 A-to-I Human chr17 + 7338472 7338472 7338472 TTTAGTAAAGACAGGGTCTCACCATGTTGGCTAAGCTGGTCTTGAACTCCTGACCTCAAATGATC TTTAGTAAAGACAGGGTCTCACCATGTTGGCTTAGCTGGTCTTGAACTCCTGACCTCAAATGATC A T ACAP1 Ensembl:ENSG00000072818 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs995964715 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181825,RMVar_hsa_circ_87945 46103 RMVar_ID_46103 Human_SNP_ID_616381664 A-to-I Human chr17 + 7338821 7338821 7338821 CTCCCACCTCAGCCTCCCAAAGTGCTGGAATTACAGGTGTGAGCCACCACACCTGGCCTGAATTT CTCCCACCTCAGCCTCCCAAAGTGCTGGAATTGCAGGTGTGAGCCACCACACCTGGCCTGAATTT A G ACAP1 Ensembl:ENSG00000072818 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1443530225 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181825,RMVar_hsa_circ_87945 46104 RMVar_ID_46104 Human_SNP_ID_616381752 A-to-I Human chr17 + 7339102 7339102 7339102 CACGAGGTCAGGAGATCGAAACCATCCTGGCTAACACTGTGAAACCCCGTCTCTACTAAAAATAC CACGAGGTCAGGAGATCGAAACCATCCTGGCTGACACTGTGAAACCCCGTCTCTACTAAAAATAC A G ACAP1 Ensembl:ENSG00000072818 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs949269789 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181825,RMVar_hsa_circ_87945 46105 RMVar_ID_46105 Human_SNP_ID_616382154 A-to-I Human chr17 + 7340680 7340680 7340680 CAGCCTGGTCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTAGCTGGGCGTGGTG CAGCCTGGTCAACATGGTGAAACCCCGTCTCTGCTAAAAATACAAAAAATTAGCTGGGCGTGGTG A G ACAP1 Ensembl:ENSG00000072818 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1050863056 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181825,RMVar_hsa_circ_87945 46106 RMVar_ID_46106 Human_SNP_ID_616382155 A-to-I Human chr17 + 7340683 7340683 7340683 CCTGGTCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTAGCTGGGCGTGGTGGCG CCTGGTCAACATGGTGAAACCCCGTCTCTACTGAAAATACAAAAAATTAGCTGGGCGTGGTGGCG A G ACAP1 Ensembl:ENSG00000072818 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs548227429 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181825,RMVar_hsa_circ_87945 46107 RMVar_ID_46107 Human_SNP_ID_616382216 A-to-I Human chr17 + 7340933 7340933 7340933 CAACTCCTGACCTCAGGTGATCCACCCACCTCAGCCTCCCAAAGTGTTGAGATTACAGGTCTGAG CAACTCCTGACCTCAGGTGATCCACCCACCTCCGCCTCCCAAAGTGTTGAGATTACAGGTCTGAG A C ACAP1 Ensembl:ENSG00000072818 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1231990202 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181825,RMVar_hsa_circ_87945 46108 RMVar_ID_46108 Human_SNP_ID_616382291 A-to-I Human chr17 + 7341174 7341173 7341175 TAGATTTTATTTATTTATTTATTTTTCGAGACAGAGTCTCGGTCTGTCACCCAGGCTGGAGTGCA TAGATTTTATTTATTTATTTATTTTTCGAGAC__AGTCTCGGTCTGTCACCCAGGCTGGAGTGCA CAG C ACAP1 Ensembl:ENSG00000072818 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1196370308 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_181825,RMVar_hsa_circ_87945 46109 RMVar_ID_46109 Human_SNP_ID_616382311 A-to-I Human chr17 + 7341311 7341220 7341311 TAACTGGGATTATAGGCACTTGGTGCCATCTCAGCTCACTACAGCCTCAGCCTCCCGGGTTCAAG _________________________________GCTCACTACAGCCTCAGCCTCCCGGGTTCAAG GGCTCACTGCAGCCTTGACCTCCCGGATTCAGGCAGTCCTCCTGCCTTAGCCCCCCAGGTAACTGGGATTATAGGCACTTGGTGCCATCTCA G ACAP1 Ensembl:ENSG00000072818 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1567628421 Functional Loss DEL dbSNP153 1..33 33 - - - RMVar_hsa_circ_181825,RMVar_hsa_circ_87945 46110 RMVar_ID_46110 Human_SNP_ID_616382348 A-to-I Human chr17 + 7341311 7341311 7341311 TAACTGGGATTATAGGCACTTGGTGCCATCTCAGCTCACTACAGCCTCAGCCTCCCGGGTTCAAG TAACTGGGATTATAGGCACTTGGTGCCATCTCGGCTCACTACAGCCTCAGCCTCCCGGGTTCAAG A G ACAP1 Ensembl:ENSG00000072818 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1233757249 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181825,RMVar_hsa_circ_87945 46111 RMVar_ID_46111 Human_SNP_ID_616382350 A-to-I Human chr17 + 7341319 7341319 7341319 ATTATAGGCACTTGGTGCCATCTCAGCTCACTACAGCCTCAGCCTCCCGGGTTCAAGCAGTCCTC ATTATAGGCACTTGGTGCCATCTCAGCTCACTGCAGCCTCAGCCTCCCGGGTTCAAGCAGTCCTC A G ACAP1 Ensembl:ENSG00000072818 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs554824937 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181825,RMVar_hsa_circ_87945 46112 RMVar_ID_46112 Human_SNP_ID_616382383 A-to-I Human chr17 + 7341422 7341422 7341422 TGCCACCATGCCTGGCTAATTTTTGAATTTTTAGTAGAGATGAGGTTTCACCATGTTGCCCAGGC TGCCACCATGCCTGGCTAATTTTTGAATTTTTTGTAGAGATGAGGTTTCACCATGTTGCCCAGGC A T ACAP1 Ensembl:ENSG00000072818 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs938593136 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_181825,RMVar_hsa_circ_87945 46113 RMVar_ID_46113 Human_SNP_ID_616420526 A-to-I Human chr17 - 7469190 7469190 7469190 TGCATTCCAGTCTGGGCGCAGAGCGAGACTCCATCTCAAAACAAATAAATAAAATTTAAAAGGAG TGCATTCCAGTCTGGGCGCAGAGCGAGACTCCGTCTCAAAACAAATAAATAAAATTTAAAAGGAG T C ZBTB4 Ensembl:ENSG00000174282 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1243167203 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13164196,Human_RBP_ID_18513865 RMVar_hsa_circ_108235,RMVar_hsa_circ_181844 46114 RMVar_ID_46114 Human_SNP_ID_616420593 A-to-I Human chr17 - 7469441 7469441 7469441 GGGAAAGTGGCCAGGCATGGAGGCTCACGCCCATAATCCCAGCACTTTGGGAGGCCTAGGTAGGC GGGAAAGTGGCCAGGCATGGAGGCTCACGCCCGTAATCCCAGCACTTTGGGAGGCCTAGGTAGGC T C ZBTB4 Ensembl:ENSG00000174282 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1345227816 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108235,RMVar_hsa_circ_181844 46115 RMVar_ID_46115 Human_SNP_ID_616420637 A-to-I Human chr17 - 7469590 7469590 7469590 TGGCTAATTTTTTTTTTATTATTATTTTTAGTAGAGATCGCCACATTGGCCAGGCTGGTCTAGAA TGGCTAATTTTTTTTTTATTATTATTTTTAGTGGAGATCGCCACATTGGCCAGGCTGGTCTAGAA T C ZBTB4 Ensembl:ENSG00000174282 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs554324516 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13164199 RMVar_hsa_circ_108235,RMVar_hsa_circ_181844 46116 RMVar_ID_46116 Human_SNP_ID_616420678 A-to-I Human chr17 - 7469765 7469765 7469765 TTTTATTTATTTTTATTTTTATTTTTTGAGACAGAGTCTCACTCTGTCACCCAGCCTGGATTGAT TTTTATTTATTTTTATTTTTATTTTTTGAGACGGAGTCTCACTCTGTCACCCAGCCTGGATTGAT T C ZBTB4 Ensembl:ENSG00000174282 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1022297363 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13241000 RMVar_hsa_circ_108235,RMVar_hsa_circ_181844 46117 RMVar_ID_46117 Human_SNP_ID_616420727 A-to-I Human chr17 - 7469960 7469960 7469960 CTCCTGCCCCAGCCTACCGAGTAGCTGGGACTACAGGTGCCTGCCACCACGTCCGGCTAATTTTT CTCCTGCCCCAGCCTACCGAGTAGCTGGGACTGCAGGTGCCTGCCACCACGTCCGGCTAATTTTT T C ZBTB4 Ensembl:ENSG00000174282 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1013409711 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108235,RMVar_hsa_circ_181844 46118 RMVar_ID_46118 Human_SNP_ID_616420892 A-to-I Human chr17 - 7470709 7470709 7470709 CCTAGCATTGATAAGCCATAATCTGACATTTTATTTATTTATTTTGAGACGAAGTTTCATTCTTG CCTAGCATTGATAAGCCATAATCTGACATTTTTTTTATTTATTTTGAGACGAAGTTTCATTCTTG T A ZBTB4 Ensembl:ENSG00000174282 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs548413666 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108235,RMVar_hsa_circ_181844 46119 RMVar_ID_46119 Human_SNP_ID_616421036 A-to-I Human chr17 - 7471276 7471276 7471276 CGGAGGCTGAGGCAGGAGGATCATTTGATTCCAGGAGGTCCAGGCTGCAGTGAGCAATGTTCACA CGGAGGCTGAGGCAGGAGGATCATTTGATTCCTGGAGGTCCAGGCTGCAGTGAGCAATGTTCACA T A ZBTB4 Ensembl:ENSG00000174282 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1289457852 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6644018,Human_RBP_ID_13164238 RMVar_hsa_circ_108235,RMVar_hsa_circ_181844 46120 RMVar_ID_46120 Human_SNP_ID_616421038 A-to-I Human chr17 - 7471295 7471295 7471295 CCTATGGTCCCAGATACTCCGGAGGCTGAGGCAGGAGGATCATTTGATTCCAGGAGGTCCAGGCT CCTATGGTCCCAGATACTCCGGAGGCTGAGGCCGGAGGATCATTTGATTCCAGGAGGTCCAGGCT T G ZBTB4 Ensembl:ENSG00000174282 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1353294982 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108235,RMVar_hsa_circ_181844 46121 RMVar_ID_46121 Human_SNP_ID_616421413 A-to-I Human chr17 - 7472766 7472766 7472766 CATTGTGGTGTGCACCTGTGGTGCCAGCTACTAGGGACGCTGAGGTGGGAGGTCATGAGAGCCTG CATTGTGGTGTGCACCTGTGGTGCCAGCTACTGGGGACGCTGAGGTGGGAGGTCATGAGAGCCTG T C ZBTB4 Ensembl:ENSG00000174282 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1323207688 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108235,RMVar_hsa_circ_181844 46122 RMVar_ID_46122 Human_SNP_ID_616421414 A-to-I Human chr17 - 7472769 7472769 7472769 GGGCATTGTGGTGTGCACCTGTGGTGCCAGCTACTAGGGACGCTGAGGTGGGAGGTCATGAGAGC GGGCATTGTGGTGTGCACCTGTGGTGCCAGCTTCTAGGGACGCTGAGGTGGGAGGTCATGAGAGC T A ZBTB4 Ensembl:ENSG00000174282 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs887759016 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108235,RMVar_hsa_circ_181844 46123 RMVar_ID_46123 Human_SNP_ID_616421415 A-to-I Human chr17 - 7472769 7472769 7472769 GGGCATTGTGGTGTGCACCTGTGGTGCCAGCTACTAGGGACGCTGAGGTGGGAGGTCATGAGAGC GGGCATTGTGGTGTGCACCTGTGGTGCCAGCTGCTAGGGACGCTGAGGTGGGAGGTCATGAGAGC T C ZBTB4 Ensembl:ENSG00000174282 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs887759016 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108235,RMVar_hsa_circ_181844 46124 RMVar_ID_46124 Human_SNP_ID_616421432 A-to-I Human chr17 - 7472843 7472843 7472843 GCCCAGGAGTTCGAGACCAGCCTGGCCAACATAGAGAGATCCAATCTCTACTAAAAATAAAAAAT GCCCAGGAGTTCGAGACCAGCCTGGCCAACATGGAGAGATCCAATCTCTACTAAAAATAAAAAAT T C ZBTB4 Ensembl:ENSG00000174282 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1001788816 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108235,RMVar_hsa_circ_181844 46125 RMVar_ID_46125 Human_SNP_ID_616421995 A-to-I Human chr17 - 7474929 7474929 7474929 CTGCTCGCTGCAACCGCCACCTCCCCGGTTCAAGCAATTCTCCTGCCTCAGCCACCTGAGTAGCT CTGCTCGCTGCAACCGCCACCTCCCCGGTTCAGGCAATTCTCCTGCCTCAGCCACCTGAGTAGCT T C ZBTB4 Ensembl:ENSG00000174282 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1186451605 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108235,RMVar_hsa_circ_181844 46126 RMVar_ID_46126 Human_SNP_ID_616422396 A-to-I Human chr17 - 7476430 7476430 7476430 TTGCCCAGGCTGGACTCAAACTCCTGGGCTCAAGCAATCCTCTAGCTGCAGCCTCCTGAGTAGCT TTGCCCAGGCTGGACTCAAACTCCTGGGCTCAGGCAATCCTCTAGCTGCAGCCTCCTGAGTAGCT T C ZBTB4 Ensembl:ENSG00000174282 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1427543687 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108235,RMVar_hsa_circ_181844 46127 RMVar_ID_46127 Human_SNP_ID_616426110 A-to-I Human chr17 + 7487193 7487193 7487193 TGTGCCACGATGCCTGGCTATTTTTGTATTTTAGTAGAGATGGGGTTTTGCCGTGTTGCCCAGGC TGTGCCACGATGCCTGGCTATTTTTGTATTTTGGTAGAGATGGGGTTTTGCCGTGTTGCCCAGGC A G POLR2A Ensembl:ENSG00000181222 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1473382237 Functional Loss SNV dbSNP153 33..33 33 - - - 46128 RMVar_ID_46128 Human_SNP_ID_616427117 A-to-I Human chr17 + 7490497 7490497 7490497 GGTCAAGAGTTCAAGACCATCCTGTCCAGCCTAGTGAAACCCCGTCTGTACTAAAAATATAAAAA GGTCAAGAGTTCAAGACCATCCTGTCCAGCCTGGTGAAACCCCGTCTGTACTAAAAATATAAAAA A G POLR2A Ensembl:ENSG00000181222 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs114325883 Functional Loss SNV dbSNP153 33..33 33 - - - 46129 RMVar_ID_46129 Human_SNP_ID_616427333 A-to-I Human chr17 + 7491289 7491289 7491289 TCAAGCGATTCTTCTGCCTCAGCCTCCCGAGTAGCAGGAACTACAGGAGCACGCCACCACACCCA TCAAGCGATTCTTCTGCCTCAGCCTCCCGAGTGGCAGGAACTACAGGAGCACGCCACCACACCCA A G POLR2A Ensembl:ENSG00000181222 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs560072586 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5510 46130 RMVar_ID_46130 Human_SNP_ID_616427349 A-to-I Human chr17 + 7491345 7491345 7491345 CCACACCCAGCTAATTTCTTTTTTGTATTTTTAGTAGAGACGGGATTTTACTGTGTTGTCCAGAC CCACACCCAGCTAATTTCTTTTTTGTATTTTTGGTAGAGACGGGATTTTACTGTGTTGTCCAGAC A G POLR2A Ensembl:ENSG00000181222 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968518474 Functional Loss SNV dbSNP153 33..33 33 - - - 46131 RMVar_ID_46131 Human_SNP_ID_616427908 A-to-I Human chr17 + 7493298 7493298 7493298 GGTGCTTATAGTTATAGGGAAGACAGACCCCCATAGGTCATTTTATTGCATTGTTGTATGTGCAG GGTGCTTATAGTTATAGGGAAGACAGACCCCCGTAGGTCATTTTATTGCATTGTTGTATGTGCAG A G POLR2A Ensembl:ENSG00000181222 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4450459 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5511,GWAS_ID_5512,GWAS_ID_5513,GWAS_ID_5514,GWAS_ID_5515,GWAS_ID_5516,GWAS_ID_5517,GWAS_ID_5518,GWAS_ID_5519,GWAS_ID_5520,GWAS_ID_5521,GWAS_ID_5522,GWAS_ID_5523,GWAS_ID_5524,GWAS_ID_5525,GWAS_ID_5526,GWAS_ID_5527,GWAS_ID_5528,GWAS_ID_5529,GWAS_ID_5530 46132 RMVar_ID_46132 Human_SNP_ID_616427909 A-to-I Human chr17 + 7493298 7493298 7493298 GGTGCTTATAGTTATAGGGAAGACAGACCCCCATAGGTCATTTTATTGCATTGTTGTATGTGCAG GGTGCTTATAGTTATAGGGAAGACAGACCCCCTTAGGTCATTTTATTGCATTGTTGTATGTGCAG A T POLR2A Ensembl:ENSG00000181222 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4450459 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5511,GWAS_ID_5512,GWAS_ID_5513,GWAS_ID_5514,GWAS_ID_5515,GWAS_ID_5516,GWAS_ID_5517,GWAS_ID_5518,GWAS_ID_5519,GWAS_ID_5520,GWAS_ID_5521,GWAS_ID_5522,GWAS_ID_5523,GWAS_ID_5524,GWAS_ID_5525,GWAS_ID_5526,GWAS_ID_5527,GWAS_ID_5528,GWAS_ID_5529,GWAS_ID_5530 46133 RMVar_ID_46133 Human_SNP_ID_616458747 A-to-I Human chr17 + 7587270 7587270 7587270 GGGCTCCCTGGCCCGAATCTTCACTTCCATTCAGGTGAGTGCAACATCTTCCTTCTAGAAGGCAC GGGCTCCCTGGCCCGAATCTTCACTTCCATTCCGGTGAGTGCAACATCTTCCTTCTAGAAGGCAC A C MPDU1 Ensembl:ENSG00000129255 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1018365142 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19081437,Human_RBP_ID_22761357 Human_Splice_Rec_1773145,Human_Splice_Rec_1773157,Human_Splice_Rec_1773167,Human_Splice_Rec_1773193,Human_Splice_Rec_1773209,Human_Splice_Rec_1773219,Human_Splice_Rec_1773227,Human_Splice_Rec_1773239,Human_Splice_Rec_1773247,Human_Splice_Rec_1773257,Human_Splice_Rec_1773285,Human_Splice_Rec_1773305,Human_Splice_Rec_1773319,Human_Splice_Rec_1773339,Human_Splice_Rec_1773355,Human_Splice_Rec_1773357 RMVar_hsa_circ_74499,RMVar_hsa_circ_88059,RMVar_hsa_circ_181912 46134 RMVar_ID_46134 Human_SNP_ID_616458748 A-to-I Human chr17 + 7587270 7587270 7587270 GGGCTCCCTGGCCCGAATCTTCACTTCCATTCAGGTGAGTGCAACATCTTCCTTCTAGAAGGCAC GGGCTCCCTGGCCCGAATCTTCACTTCCATTCGGGTGAGTGCAACATCTTCCTTCTAGAAGGCAC A G MPDU1 Ensembl:ENSG00000129255 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1018365142 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19081437,Human_RBP_ID_22761357 Human_Splice_Rec_1773145,Human_Splice_Rec_1773157,Human_Splice_Rec_1773167,Human_Splice_Rec_1773193,Human_Splice_Rec_1773209,Human_Splice_Rec_1773219,Human_Splice_Rec_1773227,Human_Splice_Rec_1773239,Human_Splice_Rec_1773247,Human_Splice_Rec_1773257,Human_Splice_Rec_1773285,Human_Splice_Rec_1773305,Human_Splice_Rec_1773319,Human_Splice_Rec_1773339,Human_Splice_Rec_1773355,Human_Splice_Rec_1773357 RMVar_hsa_circ_74499,RMVar_hsa_circ_88059,RMVar_hsa_circ_181912 46135 RMVar_ID_46135 Human_SNP_ID_616458749 A-to-I Human chr17 + 7587270 7587270 7587270 GGGCTCCCTGGCCCGAATCTTCACTTCCATTCAGGTGAGTGCAACATCTTCCTTCTAGAAGGCAC GGGCTCCCTGGCCCGAATCTTCACTTCCATTCTGGTGAGTGCAACATCTTCCTTCTAGAAGGCAC A T MPDU1 Ensembl:ENSG00000129255 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1018365142 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19081437,Human_RBP_ID_22761357 Human_Splice_Rec_1773145,Human_Splice_Rec_1773157,Human_Splice_Rec_1773167,Human_Splice_Rec_1773193,Human_Splice_Rec_1773209,Human_Splice_Rec_1773219,Human_Splice_Rec_1773227,Human_Splice_Rec_1773239,Human_Splice_Rec_1773247,Human_Splice_Rec_1773257,Human_Splice_Rec_1773285,Human_Splice_Rec_1773305,Human_Splice_Rec_1773319,Human_Splice_Rec_1773339,Human_Splice_Rec_1773355,Human_Splice_Rec_1773357 RMVar_hsa_circ_74499,RMVar_hsa_circ_88059,RMVar_hsa_circ_181912 46136 RMVar_ID_46136 Human_SNP_ID_616461931 A-to-I Human chr17 - 7597664 7597664 7597664 CGGCTCACGCCTGCAATCCCAGCACTTTGGGAAGCCGAGGCAGGTGGATTGCCTGAGGTTAGGAG CGGCTCACGCCTGCAATCCCAGCACTTTGGGAGGCCGAGGCAGGTGGATTGCCTGAGGTTAGGAG T C FXR2 Ensembl:ENSG00000129245 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1157548573 Functional Loss SNV dbSNP153 33..33 33 - - - 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 46137 RMVar_ID_46137 Human_SNP_ID_616464744 A-to-I Human chr17 - 7608395 7608395 7608395 TAGCAATGGGATTTTGCCATATTGGCCAGACTAGTCTCGAACTCATGGCCTCAGCTGATCTGCCA TAGCAATGGGATTTTGCCATATTGGCCAGACTTGTCTCGAACTCATGGCCTCAGCTGATCTGCCA T A FXR2 Ensembl:ENSG00000129245 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170114729 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13177195,Human_RBP_ID_17566764 RMVar_hsa_circ_113183,RMVar_hsa_circ_181918,RMVar_hsa_circ_94560,RMVar_hsa_circ_181923 46138 RMVar_ID_46138 Human_SNP_ID_616464749 A-to-I Human chr17 - 7608407 7608407 7608407 TTTTTTTTTTAGTAGCAATGGGATTTTGCCATATTGGCCAGACTAGTCTCGAACTCATGGCCTCA TTTTTTTTTTAGTAGCAATGGGATTTTGCCATTTTGGCCAGACTAGTCTCGAACTCATGGCCTCA T A FXR2 Ensembl:ENSG00000129245 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947845693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13177195,Human_RBP_ID_17566764 RMVar_hsa_circ_113183,RMVar_hsa_circ_181918,RMVar_hsa_circ_94560,RMVar_hsa_circ_181923 46139 RMVar_ID_46139 Human_SNP_ID_616464810 A-to-I Human chr17 - 7608535 7608535 7608535 TGACTGACTGCAGTCTCTAACTCCTGGCTTCAAGTGATTTTCATGCCTCAGCCACCCTGAATAAC TGACTGACTGCAGTCTCTAACTCCTGGCTTCAGGTGATTTTCATGCCTCAGCCACCCTGAATAAC T C FXR2 Ensembl:ENSG00000129245 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1189987947 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6647205 RMVar_hsa_circ_113183,RMVar_hsa_circ_181918,RMVar_hsa_circ_94560,RMVar_hsa_circ_181923 46140 RMVar_ID_46140 Human_SNP_ID_616481359 A-to-I Human chr17 - 7664221 7664221 7664221 AAACCCCGTCTCTACTAAAAATACAAAAAATTAGGCGGGTGTGGTGGCACGCGCCTGTAGTCCTA AAACCCCGTCTCTACTAAAAATACAAAAAATTGGGCGGGTGTGGTGGCACGCGCCTGTAGTCCTA T C TP53 Ensembl:ENSG00000141510 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1200893627 Functional Loss SNV dbSNP153 33..33 33 - - - 46141 RMVar_ID_46141 Human_SNP_ID_616482636 A-to-I Human chr17 - 7668613 7668613 7668613 GTTGCCCAGGCTGGTCTCAAACTCCTGGGCTCAGGCGATCCACCTGTCTCAGCCTCCCAGAGTGC GTTGCCCAGGCTGGTCTCAAACTCCTGGGCTCTGGCGATCCACCTGTCTCAGCCTCCCAGAGTGC T A TP53 Ensembl:ENSG00000141510 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs373069673 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_501181,Human_RBP_ID_23171957 46142 RMVar_ID_46142 Human_SNP_ID_616483366 A-to-I Human chr17 - 7670940 7670940 7670940 TTGAACCCCAGAGGCGGAGATTGCAATCAGCCAAGATTGCACCATTGCACTCCCGCCTGGGCAAC TTGAACCCCAGAGGCGGAGATTGCAATCAGCCGAGATTGCACCATTGCACTCCCGCCTGGGCAAC T C TP53 Ensembl:ENSG00000141510 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs896682837 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20059,RMVar_hsa_circ_327628,RMVar_hsa_circ_348580,RMVar_hsa_circ_181926,RMVar_hsa_circ_181927 46143 RMVar_ID_46143 Human_SNP_ID_616483367 A-to-I Human chr17 - 7670947 7670947 7670947 GAATCACTTGAACCCCAGAGGCGGAGATTGCAATCAGCCAAGATTGCACCATTGCACTCCCGCCT GAATCACTTGAACCCCAGAGGCGGAGATTGCAGTCAGCCAAGATTGCACCATTGCACTCCCGCCT T C TP53 Ensembl:ENSG00000141510 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1426991081 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20059,RMVar_hsa_circ_327628,RMVar_hsa_circ_348580,RMVar_hsa_circ_181926,RMVar_hsa_circ_181927 46144 RMVar_ID_46144 Human_SNP_ID_616483634 A-to-I Human chr17 - 7672059 7672059 7672059 TAAAGACAGAGTCTCACTCTGTCACTCAGGCTAGAGTGCAGTGGCACCATCTCAGCTCACTGCAG TAAAGACAGAGTCTCACTCTGTCACTCAGGCTGGAGTGCAGTGGCACCATCTCAGCTCACTGCAG T C TP53 Ensembl:ENSG00000141510 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1208611830 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20059,RMVar_hsa_circ_327628,RMVar_hsa_circ_348580,RMVar_hsa_circ_181926,RMVar_hsa_circ_181927 46145 RMVar_ID_46145 Human_SNP_ID_616541703 A-to-I Human chr17 - 7867552 7867552 7867552 CCACACGGGTGGATTGTCAGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCCCGTCTCTAC CCACACGGGTGGATTGTCAGGAGTTCAAGACCCGCCTGGCCAACATGGTGAAACCCCGTCTCTAC T G NAA38 Ensembl:ENSG00000183011 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1393359147 Functional Loss SNV dbSNP153 33..33 33 - - - 46146 RMVar_ID_46146 Human_SNP_ID_616541717 A-to-I Human chr17 - 7867611 7867611 7867611 CCCTTAACTCTGGGCCAGGTACAGTGGCTCACACCTGTAATCCCAGCACTGTGGGAGGCCCACAC CCCTTAACTCTGGGCCAGGTACAGTGGCTCACTCCTGTAATCCCAGCACTGTGGGAGGCCCACAC T A NAA38 Ensembl:ENSG00000183011 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs534272247 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20295428 46147 RMVar_ID_46147 Human_SNP_ID_616541718 A-to-I Human chr17 - 7867611 7867611 7867611 CCCTTAACTCTGGGCCAGGTACAGTGGCTCACACCTGTAATCCCAGCACTGTGGGAGGCCCACAC CCCTTAACTCTGGGCCAGGTACAGTGGCTCACGCCTGTAATCCCAGCACTGTGGGAGGCCCACAC T C NAA38 Ensembl:ENSG00000183011 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs534272247 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20295428 46148 RMVar_ID_46148 Human_SNP_ID_616541724 A-to-I Human chr17 - 7867623 7867623 7867623 CTCTCTATAAAACCCTTAACTCTGGGCCAGGTACAGTGGCTCACACCTGTAATCCCAGCACTGTG CTCTCTATAAAACCCTTAACTCTGGGCCAGGTTCAGTGGCTCACACCTGTAATCCCAGCACTGTG T A NAA38 Ensembl:ENSG00000183011 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1331749249 Functional Loss SNV dbSNP153 33..33 33 - - - 46149 RMVar_ID_46149 Human_SNP_ID_616542602 A-to-I Human chr17 - 7871730 7871730 7871730 GAATTGCTTGAACTCGGGAGGCGGAGGTTGCAATGAGCCAAGATTGCACCACTGCACTCCAGCCT GAATTGCTTGAACTCGGGAGGCGGAGGTTGCAGTGAGCCAAGATTGCACCACTGCACTCCAGCCT T C NAA38 Ensembl:ENSG00000183011 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs556010688 Functional Loss SNV dbSNP153 33..33 33 - - - 46150 RMVar_ID_46150 Human_SNP_ID_616543329 A-to-I Human chr17 - 7875003 7875003 7875003 TTTGTAGAGATGGGATCTCGCTGTGTCGTTCAAATTGGTCTTAAACTCTTGGCCTCAAGCGATCC TTTGTAGAGATGGGATCTCGCTGTGTCGTTCACATTGGTCTTAAACTCTTGGCCTCAAGCGATCC T G NAA38 Ensembl:ENSG00000183011 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs182813299 Functional Loss SNV dbSNP153 33..33 33 - - - 46151 RMVar_ID_46151 Human_SNP_ID_616543341 A-to-I Human chr17 + 7875043 7875043 7875043 CACAGCGAGATCCCATCTCTACAAAAAATTTTAAAACTATCCGGTTGTGGTGGTGTGTGCCTGTA CACAGCGAGATCCCATCTCTACAAAAAATTTTGAAACTATCCGGTTGTGGTGGTGTGTGCCTGTA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264714780 Functional Loss SNV dbSNP153 33..33 33 - - - 46152 RMVar_ID_46152 Human_SNP_ID_616543351 A-to-I Human chr17 - 7875086 7875086 7875086 GGCTCAAGCTTTCCTCCTCCCTCATCCTCCCAAGTAGCTGGACTACAGGCACACACCACCACAAC GGCTCAAGCTTTCCTCCTCCCTCATCCTCCCAGGTAGCTGGACTACAGGCACACACCACCACAAC T C NAA38 Ensembl:ENSG00000183011 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270171943 Functional Loss SNV dbSNP153 33..33 33 - - - 46153 RMVar_ID_46153 Human_SNP_ID_616550589 A-to-I Human chr17 + 7902366 7902366 7902366 ATCACTTGAACCCAGGAGTGGAGGTTGCAGTGAGCAGAGATGGCACCACTGCACTCCAGCTAGGG ATCACTTGAACCCAGGAGTGGAGGTTGCAGTGGGCAGAGATGGCACCACTGCACTCCAGCTAGGG A G CHD3 Ensembl:ENSG00000170004 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1309258581 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23308678 RMVar_hsa_circ_181956,RMVar_hsa_circ_103898,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_181957,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_24146,RMVar_hsa_circ_14270 46154 RMVar_ID_46154 Human_SNP_ID_616550878 A-to-I Human chr17 - 7903505 7903505 7903505 CCTGCTTTCACAGAGCTGCAGAAAAGGTTCTCACCCTCGTTTTCATCCTTGAATAGCTCTTCAGT CCTGCTTTCACAGAGCTGCAGAAAAGGTTCTCCCCCTCGTTTTCATCCTTGAATAGCTCTTCAGT T G - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1329252017 Functional Loss SNV dbSNP153 33..33 33 - - - 46155 RMVar_ID_46155 Human_SNP_ID_616553394 A-to-I Human chr17 + 7911910 7911910 7911910 CACAACTTCCCAGTAAATGGTTGTGGGGAGGAAAGAGGTGGAGCCTCCCCAGCCGTTTCCCTGCA CACAACTTCCCAGTAAATGGTTGTGGGGAGGACAGAGGTGGAGCCTCCCCAGCCGTTTCCCTGCA A C CHD3 Ensembl:ENSG00000170004 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs997778313 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27458319 RMVar_hsa_circ_119752,RMVar_hsa_circ_181965,RMVar_hsa_circ_181978 46156 RMVar_ID_46156 Human_SNP_ID_616558918 A-to-I Human chr17 - 7931124 7931124 7931124 TCTGCAGGAAGGATGGCTTCCTGGCCTTCCAAACTAGCCGTTACAAACTCCATTACTACGAGACG TCTGCAGGAAGGATGGCTTCCTGGCCTTCCAATCTAGCCGTTACAAACTCCATTACTACGAGACG T A TRAPPC1 Ensembl:ENSG00000170043 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs753606156 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_502122,Human_RBP_ID_1184778,Human_RBP_ID_1289352,Human_RBP_ID_1544077,Human_RBP_ID_8465280,Human_RBP_ID_9076852,Human_RBP_ID_17262291,Human_RBP_ID_18710774,Human_RBP_ID_26811930 Human_Splice_Rec_1775426,Human_Splice_Rec_1775432,Human_Splice_Rec_1775438,Human_Splice_Rec_1775442,Human_Splice_Rec_1775450,Human_Splice_Rec_1775456 RMVar_hsa_circ_181981,RMVar_hsa_circ_78714 46157 RMVar_ID_46157 Human_SNP_ID_616561688 A-to-I Human chr17 + 7941350 7941350 7941350 GGCCCGGTATGGTGGCTCATGCCTGTAATCCCAGCACTGTGGGAGGCCAAGGCGGGTGGATCACT GGCCCGGTATGGTGGCTCATGCCTGTAATCCCGGCACTGTGGGAGGCCAAGGCGGGTGGATCACT A G CNTROB Ensembl:ENSG00000170037 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1475646085 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_65332,RMVar_hsa_circ_20441,RMVar_hsa_circ_18274,RMVar_hsa_circ_54922,RMVar_hsa_circ_19764,RMVar_hsa_circ_356758 46158 RMVar_ID_46158 Human_SNP_ID_616561854 A-to-I Human chr17 + 7941891 7941891 7941891 AGGCTGAGGTGGGAGGATCAACTGAACCCTGGAAGTAGAGGCTGCAGTGACCCGTGATCACACCA AGGCTGAGGTGGGAGGATCAACTGAACCCTGGCAGTAGAGGCTGCAGTGACCCGTGATCACACCA A C CNTROB Ensembl:ENSG00000170037 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs980418997 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_65332,RMVar_hsa_circ_20441,RMVar_hsa_circ_18274,RMVar_hsa_circ_54922,RMVar_hsa_circ_19764,RMVar_hsa_circ_356758 46159 RMVar_ID_46159 Human_SNP_ID_616628793 A-to-I Human chr17 - 8172775 8172775 8172775 GGGATCATGGCTCACTGCAGCCTCAAACTCCCAGGCTCAGATGATCCTCCTGCATCAGCCTCCCA GGGATCATGGCTCACTGCAGCCTCAAACTCCCGGGCTCAGATGATCCTCCTGCATCAGCCTCCCA T C TMEM107 Ensembl:ENSG00000179029 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs997663491 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6654320 46160 RMVar_ID_46160 Human_SNP_ID_616630690 A-to-I Human chr17 - 8176028 8176028 8176028 CTTTTTCACTTCTCTTCCTGTGCCCTGCTCCCAGGACAGCAACATACAGGCCTGCCTGCCTCTCA CTTTTTCACTTCTCTTCCTGTGCCCTGCTCCCGGGACAGCAACATACAGGCCTGCCTGCCTCTCA T C TMEM107 Ensembl:ENSG00000179029 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1381990873 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1776323,Human_Splice_Rec_1776333,Human_Splice_Rec_1776337,Human_Splice_Rec_1776345,Human_Splice_Rec_1776353 46161 RMVar_ID_46161 Human_SNP_ID_616630735 A-to-I Human chr17 + 8176140 8176140 8176140 CAAGAGGGTAAGACACTGGGAGGGGGCAGGGTAGGACTAGGACCACTCAGAGATGGGAATGGGGA CAAGAGGGTAAGACACTGGGAGGGGGCAGGGTGGGACTAGGACCACTCAGAGATGGGAATGGGGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs528521526 Functional Loss SNV dbSNP153 33..33 33 - - - 46162 RMVar_ID_46162 Human_SNP_ID_616634887 A-to-I Human chr17 + 8187627 8187625 8187628 CCGGTTAGCTCAGTTGGTTAGAGCGTGGTGCTAATAACGCCAAGGTCGCGGGTTCGATCCCCGTA CCGGTTAGCTCAGTTGGTTAGAGCGTGGTGC___TAACGCCAAGGTCGCGGGTTCGATCCCCGTA CTAA C tRNA-Ile-AAT-5-4 RNACentral:URS0000610FFE tRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1362506595 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_4462820,Human_RBP_ID_18713085,Human_RBP_ID_22807754,Human_RBP_ID_22958846 46163 RMVar_ID_46163 Human_SNP_ID_616646462 A-to-I Human chr17 + 8224937 8224937 8224937 GCTGACAACACCTCCTCCCCCCTCCAAGGTTGAAGCGATTCTCTTGCCTCAGCCTCCCAAGTAGC GCTGACAACACCTCCTCCCCCCTCCAAGGTTGGAGCGATTCTCTTGCCTCAGCCTCCCAAGTAGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1183074647 Functional Loss SNV dbSNP153 33..33 33 - - - 46164 RMVar_ID_46164 Human_SNP_ID_616655103 A-to-I Human chr17 + 8252044 8252044 8252044 GGGTCGGAATGGTGGCGCACGCCTGTAATCCCAACGCTTTGGGAGTCCGAGGCGGGCAGATCACT GGGTCGGAATGGTGGCGCACGCCTGTAATCCCGACGCTTTGGGAGTCCGAGGCGGGCAGATCACT A G PFAS Ensembl:ENSG00000178921 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs960110303 Functional Loss SNV dbSNP153 33..33 33 - - - 46165 RMVar_ID_46165 Human_SNP_ID_616660966 A-to-I Human chr17 + 8269899 8269899 8269899 AATTAGCAGCTCTCTTTTTTTTTTTTTTTTTGAGGCAGTCTCACTCTGTCACCCAGGCTGGAGTA AATTAGCAGCTCTCTTTTTTTTTTTTTTTTTGTGGCAGTCTCACTCTGTCACCCAGGCTGGAGTA A T PFAS Ensembl:ENSG00000178921 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1169834726 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6654753,Human_RBP_ID_13213805 RMVar_hsa_circ_84505,RMVar_hsa_circ_182029 46166 RMVar_ID_46166 Human_SNP_ID_616660992 A-to-I Human chr17 + 8269977 8269977 8269977 TCGGCCCACTGCAACCTCTGCCTCCTGGGTTCAAGCAATTTTCCTGCCTCAGCCTCCCGAGTAGC TCGGCCCACTGCAACCTCTGCCTCCTGGGTTCCAGCAATTTTCCTGCCTCAGCCTCCCGAGTAGC A C PFAS Ensembl:ENSG00000178921 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1003738529 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84505,RMVar_hsa_circ_182029 46167 RMVar_ID_46167 Human_SNP_ID_616660993 A-to-I Human chr17 + 8269981 8269981 8269981 CCCACTGCAACCTCTGCCTCCTGGGTTCAAGCAATTTTCCTGCCTCAGCCTCCCGAGTAGCTGGG CCCACTGCAACCTCTGCCTCCTGGGTTCAAGCGATTTTCCTGCCTCAGCCTCCCGAGTAGCTGGG A G PFAS Ensembl:ENSG00000178921 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE99789;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,24183664,29129909,29796672,29796672,31158229,31158229,31158229 RNA-Seq:(High) rs1156905743 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25333794 RMVar_hsa_circ_84505,RMVar_hsa_circ_182029 46168 RMVar_ID_46168 Human_SNP_ID_616661006 A-to-I Human chr17 + 8270043 8270043 8270043 GGGAGTACAGGCACACACCACCACACCCAGCTAATTTTTGTATTTTTAGTAGAGATAGGGTTTCA GGGAGTACAGGCACACACCACCACACCCAGCTGATTTTTGTATTTTTAGTAGAGATAGGGTTTCA A G PFAS Ensembl:ENSG00000178921 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs765849761 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84505,RMVar_hsa_circ_182029 46169 RMVar_ID_46169 Human_SNP_ID_616661009 A-to-I Human chr17 + 8270052 8270052 8270052 GGCACACACCACCACACCCAGCTAATTTTTGTATTTTTAGTAGAGATAGGGTTTCACCATGTCTC GGCACACACCACCACACCCAGCTAATTTTTGTGTTTTTAGTAGAGATAGGGTTTCACCATGTCTC A G PFAS Ensembl:ENSG00000178921 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs911262619 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13244155 Human_miRNA_ID_753357,Human_miRNA_ID_1175877,Human_miRNA_ID_1628560,Human_miRNA_ID_1669058 RMVar_hsa_circ_84505,RMVar_hsa_circ_182029 46170 RMVar_ID_46170 Human_SNP_ID_616661019 A-to-I Human chr17 + 8270075 8270075 8270075 AATTTTTGTATTTTTAGTAGAGATAGGGTTTCACCATGTCTCCCAGGCTGGTCTCAAACTCCTAA AATTTTTGTATTTTTAGTAGAGATAGGGTTTCGCCATGTCTCCCAGGCTGGTCTCAAACTCCTAA A G PFAS Ensembl:ENSG00000178921 Protein coding 3'UTR GSE47997;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 K562 cells&HepG2 cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 23474544,29129909,31158229 RNA-Seq:(High) rs1264225476 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13213809,Human_RBP_ID_17378086,Human_RBP_ID_17494791,Human_RBP_ID_26456862 RMVar_hsa_circ_84505,RMVar_hsa_circ_182029 46171 RMVar_ID_46171 Human_SNP_ID_616661020 A-to-I Human chr17 + 8270078 8270078 8270078 TTTTGTATTTTTAGTAGAGATAGGGTTTCACCATGTCTCCCAGGCTGGTCTCAAACTCCTAACCT TTTTGTATTTTTAGTAGAGATAGGGTTTCACCGTGTCTCCCAGGCTGGTCTCAAACTCCTAACCT A G PFAS Ensembl:ENSG00000178921 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1132556 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13213809,Human_RBP_ID_17378086,Human_RBP_ID_17494791,Human_RBP_ID_26456862 RMVar_hsa_circ_84505,RMVar_hsa_circ_182029 46172 RMVar_ID_46172 Human_SNP_ID_616661414 A-to-I Human chr17 + 8271820 8271820 8271820 AAAATTAGCTGGGTGTGGTGGTGTGTGCCAATAATCCCAGCTTCTCGGGAGGCTGAGGCAGAAGA AAAATTAGCTGGGTGTGGTGGTGTGTGCCAATTATCCCAGCTTCTCGGGAGGCTGAGGCAGAAGA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs908839183 Functional Loss SNV dbSNP153 33..33 33 - - - 46173 RMVar_ID_46173 Human_SNP_ID_616661421 A-to-I Human chr17 + 8271849 8271849 8271849 AATAATCCCAGCTTCTCGGGAGGCTGAGGCAGAAGAATCGCTTGAACCCAGGAGGCGGAGGTTGC AATAATCCCAGCTTCTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCAGGAGGCGGAGGTTGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1468612842 Functional Loss SNV dbSNP153 33..33 33 - - - 46174 RMVar_ID_46174 Human_SNP_ID_616662872 A-to-I Human chr17 + 8277776 8277775 8277776 CCTGACCAACATGGAGAAACCTCGTCTCTACTAAAAACACAAAATTATCCGGGCATGGTGGCACA CCTGACCAACATGGAGAAACCTCGTCTCTACT_AAAACACAAAATTATCCGGGCATGGTGGCACA TA T AC135178.6 Ensembl:ENSG00000269947 lincRNA exon GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1205643027 Functional Loss DEL dbSNP153 33..33 33 - - - 46175 RMVar_ID_46175 Human_SNP_ID_616662873 A-to-I Human chr17 + 8277776 8277776 8277776 CCTGACCAACATGGAGAAACCTCGTCTCTACTAAAAACACAAAATTATCCGGGCATGGTGGCACA CCTGACCAACATGGAGAAACCTCGTCTCTACTGAAAACACAAAATTATCCGGGCATGGTGGCACA A G AC135178.6 Ensembl:ENSG00000269947 lincRNA exon GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs979720014 Functional Loss SNV dbSNP153 33..33 33 - - - 46176 RMVar_ID_46176 Human_SNP_ID_616662874 A-to-I Human chr17 + 8277776 8277776 8277776 CCTGACCAACATGGAGAAACCTCGTCTCTACTAAAAACACAAAATTATCCGGGCATGGTGGCACA CCTGACCAACATGGAGAAACCTCGTCTCTACTTAAAACACAAAATTATCCGGGCATGGTGGCACA A T AC135178.6 Ensembl:ENSG00000269947 lincRNA exon GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs979720014 Functional Loss SNV dbSNP153 33..33 33 - - - 46177 RMVar_ID_46177 Human_SNP_ID_616684312 A-to-I Human chr17 - 8357802 8357801 8357802 AATTAGGCCAGGTGTGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGAGTGGA AATTAGGCCAGGTGTGGTGGCTCATGCCTGTA_TCCCAGCACTTTGGGAGGCCGAGGCGAGTGGA AT A KRBA2 Ensembl:ENSG00000184619 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1242243098 Functional Loss DEL dbSNP153 33..33 33 - - - 46178 RMVar_ID_46178 Human_SNP_ID_616684534 A-to-I Human chr17 - 8358600 8358600 8358600 GATCATGAGGTCAGAAGTTCGAGACCAGCCTAACCAACATGGTGAAACCCCGTCTCTACAAAAAT GATCATGAGGTCAGAAGTTCGAGACCAGCCTAGCCAACATGGTGAAACCCCGTCTCTACAAAAAT T C KRBA2 Ensembl:ENSG00000184619 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs960092945 Functional Loss SNV dbSNP153 33..33 33 - - - 46179 RMVar_ID_46179 Human_SNP_ID_616685289 A-to-I Human chr17 - 8361828 8361828 8361828 CATCTTCCCTGCTCAAGAATCTCCATTGGGCCAGGTGCAGTGGCTCGTGCCTGTAATCCAAGCAC CATCTTCCCTGCTCAAGAATCTCCATTGGGCCGGGTGCAGTGGCTCGTGCCTGTAATCCAAGCAC T C KRBA2 Ensembl:ENSG00000184619 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879943994 Functional Loss SNV dbSNP153 33..33 33 - - - 46180 RMVar_ID_46180 Human_SNP_ID_616685656 A-to-I Human chr17 - 8363642 8363642 8363642 AATAATGCCATTTAAAAAGTAGAAAATAGGCTAGGTGCAGTGGCTCATGCCTGTAATCCCAGCAC AATAATGCCATTTAAAAAGTAGAAAATAGGCTGGGTGCAGTGGCTCATGCCTGTAATCCCAGCAC T C KRBA2 Ensembl:ENSG00000184619 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs912870646 Functional Loss SNV dbSNP153 33..33 33 - - - 46181 RMVar_ID_46181 Human_SNP_ID_616686788 A-to-I Human chr17 - 8367423 8367423 8367423 ATGATCTGGGCTCACTGCAGCCTCCGCCTCCCAGGTTTAAGCGATTCTCCTGCCTCAGCCTCCTG ATGATCTGGGCTCACTGCAGCCTCCGCCTCCCCGGTTTAAGCGATTCTCCTGCCTCAGCCTCCTG T G KRBA2 Ensembl:ENSG00000184619 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1468711977 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_504161 46182 RMVar_ID_46182 Human_SNP_ID_616687013 A-to-I Human chr17 - 8368050 8368050 8368050 TAGGGTCTCCTTATATTGCCCAGGCTGGTCTCAAACTCCTGGGCCCAAGGGATTGGCCTCCCAAA TAGGGTCTCCTTATATTGCCCAGGCTGGTCTCGAACTCCTGGGCCCAAGGGATTGGCCTCCCAAA T C KRBA2 Ensembl:ENSG00000184619 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1397772500 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13214626 46183 RMVar_ID_46183 Human_SNP_ID_616687081 A-to-I Human chr17 - 8368374 8368374 8368374 AGGCCATAATTTTTTATGGCAGCCCTAAGAATAAATACACAGACCCGAACTTTTCCCTTATTAAG AGGCCATAATTTTTTATGGCAGCCCTAAGAATGAATACACAGACCCGAACTTTTCCCTTATTAAG T C KRBA2 Ensembl:ENSG00000184619 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903742221 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13214638 46184 RMVar_ID_46184 Human_SNP_ID_616687082 A-to-I Human chr17 - 8368379 8368379 8368379 TGAGAAGGCCATAATTTTTTATGGCAGCCCTAAGAATAAATACACAGACCCGAACTTTTCCCTTA TGAGAAGGCCATAATTTTTTATGGCAGCCCTAGGAATAAATACACAGACCCGAACTTTTCCCTTA T C KRBA2 Ensembl:ENSG00000184619 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs926764115 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13214641 46185 RMVar_ID_46185 Human_SNP_ID_616687192 A-to-I Human chr17 - 8368838 8368838 8368838 GAGATCAGGAGTTCAAGACTAGCCTGGCCAACATGATGAAACCCTGTCTCTACTGAAAATATAGA GAGATCAGGAGTTCAAGACTAGCCTGGCCAACGTGATGAAACCCTGTCTCTACTGAAAATATAGA T C KRBA2,AC135178.3 Ensembl:ENSG00000184619,Ensembl:ENSG00000263809 Protein coding,Protein coding intron,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1415276136 Functional Loss SNV dbSNP153 33..33 33 - - - 46186 RMVar_ID_46186 Human_SNP_ID_616687198 A-to-I Human chr17 - 8368856 8368856 8368856 AAGGTGGGCGGGTCACTTGAGATCAGGAGTTCAAGACTAGCCTGGCCAACATGATGAAACCCTGT AAGGTGGGCGGGTCACTTGAGATCAGGAGTTCGAGACTAGCCTGGCCAACATGATGAAACCCTGT T C KRBA2,AC135178.3 Ensembl:ENSG00000184619,Ensembl:ENSG00000263809 Protein coding,Protein coding intron,3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1418098181 Functional Loss SNV dbSNP153 33..33 33 - - - 46187 RMVar_ID_46187 Human_SNP_ID_616687240 A-to-I Human chr17 - 8369030 8369030 8369030 CCCCAGAGGAAAAGATTGAAGGCTGCACTCTCAGGTCAAGTTGTACATGGCAGTCCTTGCTCAAA CCCCAGAGGAAAAGATTGAAGGCTGCACTCTCTGGTCAAGTTGTACATGGCAGTCCTTGCTCAAA T A KRBA2,AC135178.3 Ensembl:ENSG00000184619,Ensembl:ENSG00000263809 Protein coding,Protein coding intron,3'UTR GSE100210;GSE107867 HepG2 cell line;ASD brains,cerebellum - 29129909,30559470 RNA-Seq:(High) rs1040702929 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6654949,Human_RBP_ID_13214667,Human_RBP_ID_17903852 46188 RMVar_ID_46188 Human_SNP_ID_616691977 A-to-I Human chr17 + 8384304 8384304 8384304 TTTTGTAGTTTTAGTAGAGACGAGGGTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCCGACCT TTTTGTAGTTTTAGTAGAGACGAGGGTTCACCGTGTTGGCCAGGCTGGTCTCGAACTCCCGACCT A G lnc-NDEL1-5 RNACentral:URS0000D5E17E lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1045715523 Functional Loss SNV dbSNP153 33..33 33 - - - 46189 RMVar_ID_46189 Human_SNP_ID_616726592 A-to-I Human chr17 + 8518334 8518334 8518334 TTTTGTATTTTTAGTAGAGATGGGGTTTTGCCATGAAGCCCTGGCTGGTCTCGAACTCCTGAGCT TTTTGTATTTTTAGTAGAGATGGGGTTTTGCCGTGAAGCCCTGGCTGGTCTCGAACTCCTGAGCT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1320281771 Functional Loss SNV dbSNP153 33..33 33 - - - 46190 RMVar_ID_46190 Human_SNP_ID_616805899 A-to-I Human chr17 - 8833786 8833786 8833786 CCTGTAATCCCAACACTTTGGGAGGCCAAGGCAGGCAGATCATGAGGTCAGGAGATCGAGACCGT CCTGTAATCCCAACACTTTGGGAGGCCAAGGCGGGCAGATCATGAGGTCAGGAGATCGAGACCGT T C PIK3R6 Ensembl:ENSG00000276231 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1027072845 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_182085,RMVar_hsa_circ_113388 46191 RMVar_ID_46191 Human_SNP_ID_616809378 A-to-I Human chr17 - 8847702 8847702 8847702 ACCTCCCAGGTTCAAGCGATTCTCCAGCCTCAACCTCCCAAGTAGCTGGGATTACAGGCATGCAC ACCTCCCAGGTTCAAGCGATTCTCCAGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCATGCAC T C PIK3R6 Ensembl:ENSG00000276231 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs903060307 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_182085,RMVar_hsa_circ_113388 46192 RMVar_ID_46192 Human_SNP_ID_616810806 A-to-I Human chr17 - 8853296 8853296 8853296 TATTTTTAGTAGAGACGGGGTTTCACCATGTTAGCCAGGATGGTCTCCATCTGCTGATCCTGTGA TATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGATGGTCTCCATCTGCTGATCCTGTGA T C PIK3R6 Ensembl:ENSG00000276231 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1340380402 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_182085,RMVar_hsa_circ_113388 46193 RMVar_ID_46193 Human_SNP_ID_616811967 A-to-I Human chr17 - 8857742 8857739 8857742 GCACCTGCCGCCACACCCAGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTAG GCACCTGCCGCCACACCCAGCTAATTTTTTGT___TTTAGTAGAGACGGGGTTTCACCATGTTAG AAAT A PIK3R6 Ensembl:ENSG00000276231 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs79848717 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_182085,RMVar_hsa_circ_113388 46194 RMVar_ID_46194 Human_SNP_ID_616827357 A-to-I Human chr17 - 8919872 8919872 8919872 AAAAAAAAAAAAAAAAGAAGGAAAAAGAAAAAAAGAGAAAGAAAGAAAGAGAGAGAGAGAGAAGG AAAAAAAAAAAAAAAAGAAGGAAAAAGAAAAAGAGAGAAAGAAAGAAAGAGAGAGAGAGAGAAGG T C PIK3R5 Ensembl:ENSG00000141506 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs886580830 Functional Loss SNV dbSNP153 33..33 33 - - - 46195 RMVar_ID_46195 Human_SNP_ID_616928537 A-to-I Human chr17 - 9308414 9308414 9308414 GGCTGTAATTCCTTTTCACCAAGGTGAGTCATAGGAACTAGAACCTTTCTCCCTCAAAACGTAGA GGCTGTAATTCCTTTTCACCAAGGTGAGTCATGGGAACTAGAACCTTTCTCCCTCAAAACGTAGA T C STX8 Ensembl:ENSG00000170310 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs527583151 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118911,RMVar_hsa_circ_124943,RMVar_hsa_circ_97691,RMVar_hsa_circ_182092,RMVar_hsa_circ_182093,RMVar_hsa_circ_182091 46196 RMVar_ID_46196 Human_SNP_ID_616939465 A-to-I Human chr17 - 9349238 9349238 9349238 TCTGTAATCTAAGCACTTTAGCAGGCCGAGGTAGGCAGATCACCCAAGGTCAGGAGTTTGAGACC TCTGTAATCTAAGCACTTTAGCAGGCCGAGGTGGGCAGATCACCCAAGGTCAGGAGTTTGAGACC T C STX8 Ensembl:ENSG00000170310 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1007578789 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118911,RMVar_hsa_circ_124943,RMVar_hsa_circ_97691,RMVar_hsa_circ_182092,RMVar_hsa_circ_182093,RMVar_hsa_circ_182091 46197 RMVar_ID_46197 Human_SNP_ID_616940165 A-to-I Human chr17 - 9351898 9351898 9351898 GTGATCCTCCCAAGTCGGCCTCCCAAAGCGCTAGGATTACAGGACACAGTACACTGCTCCAAATT GTGATCCTCCCAAGTCGGCCTCCCAAAGCGCTGGGATTACAGGACACAGTACACTGCTCCAAATT T C STX8 Ensembl:ENSG00000170310 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1028050640 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118911,RMVar_hsa_circ_124943,RMVar_hsa_circ_97691,RMVar_hsa_circ_182092,RMVar_hsa_circ_182093,RMVar_hsa_circ_182091 46198 RMVar_ID_46198 Human_SNP_ID_616940211 A-to-I Human chr17 - 9352075 9352075 9352075 CAATCGTAGCTCACCGAAGCCCTCCATCTTCCAGGCTCAAACAATCCTCCTGCCTCAGCCTCCCA CAATCGTAGCTCACCGAAGCCCTCCATCTTCCGGGCTCAAACAATCCTCCTGCCTCAGCCTCCCA T C STX8 Ensembl:ENSG00000170310 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1240981833 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118911,RMVar_hsa_circ_124943,RMVar_hsa_circ_97691,RMVar_hsa_circ_182092,RMVar_hsa_circ_182093,RMVar_hsa_circ_182091 46199 RMVar_ID_46199 Human_SNP_ID_616973123 A-to-I Human chr17 - 9474511 9474511 9474511 GAATTGTTGGCTACCCAGTTAGTGGCACCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA GAATTGTTGGCTACCCAGTTAGTGGCACCTGTGGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA T C STX8 Ensembl:ENSG00000170310 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285288286 Functional Loss SNV dbSNP153 33..33 33 - - - 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 46200 RMVar_ID_46200 Human_SNP_ID_616974947 A-to-I Human chr17 - 9482177 9482177 9482177 TTGCTGTAAGACGATTAAAAAAAAATAGGGACAGGGTCTTGCTGTGTTGCTCAGGCTGGAATGCA TTGCTGTAAGACGATTAAAAAAAAATAGGGACGGGGTCTTGCTGTGTTGCTCAGGCTGGAATGCA T C STX8 Ensembl:ENSG00000170310 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs766953720 Functional Loss SNV dbSNP153 33..33 33 - - - 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 46201 RMVar_ID_46201 Human_SNP_ID_616994043 A-to-I Human chr17 - 9555844 9555844 9555844 TTGCCCAGGCTGGAGTGCAGCGGTGCGATCTCAGCTCACTGCAAGCTCTGCCTCCCGGGTTCATG TTGCCCAGGCTGGAGTGCAGCGGTGCGATCTCGGCTCACTGCAAGCTCTGCCTCCCGGGTTCATG T C STX8 Ensembl:ENSG00000170310 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1424690016 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118911,RMVar_hsa_circ_124943,RMVar_hsa_circ_182092,RMVar_hsa_circ_182093,RMVar_hsa_circ_284103,RMVar_hsa_circ_345052 46202 RMVar_ID_46202 Human_SNP_ID_616994209 A-to-I Human chr17 - 9556630 9556630 9556630 CGAGACCAGCCTGGTCAACATGGTGAAACCCCATCTCTACTGAAAATATAAAAATTAGCTGGGCG CGAGACCAGCCTGGTCAACATGGTGAAACCCCGTCTCTACTGAAAATATAAAAATTAGCTGGGCG T C STX8 Ensembl:ENSG00000170310 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1344288978 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118911,RMVar_hsa_circ_124943,RMVar_hsa_circ_182092,RMVar_hsa_circ_182093,RMVar_hsa_circ_284103,RMVar_hsa_circ_345052 46203 RMVar_ID_46203 Human_SNP_ID_616994218 A-to-I Human chr17 - 9556645 9556645 9556645 TTGAGGCCAGGAGTTCGAGACCAGCCTGGTCAACATGGTGAAACCCCATCTCTACTGAAAATATA TTGAGGCCAGGAGTTCGAGACCAGCCTGGTCAGCATGGTGAAACCCCATCTCTACTGAAAATATA T C STX8 Ensembl:ENSG00000170310 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1026400270 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118911,RMVar_hsa_circ_124943,RMVar_hsa_circ_182092,RMVar_hsa_circ_182093,RMVar_hsa_circ_284103,RMVar_hsa_circ_345052 46204 RMVar_ID_46204 Human_SNP_ID_617026326 A-to-I Human chr17 + 9682497 9682497 9682497 GAGGCTGAGACAGGAGAATCATTTGAACCTGGAAGGTAGAGTTTGCAGTGAGCCAAGATTGTGCC GAGGCTGAGACAGGAGAATCATTTGAACCTGGGAGGTAGAGTTTGCAGTGAGCCAAGATTGTGCC A G USP43 Ensembl:ENSG00000154914 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1436791768 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43049,RMVar_hsa_circ_335138,RMVar_hsa_circ_368545,RMVar_hsa_circ_9495,RMVar_hsa_circ_182097,RMVar_hsa_circ_182098,RMVar_hsa_circ_5957,RMVar_hsa_circ_3897,RMVar_hsa_circ_298840,RMVar_hsa_circ_335161,RMVar_hsa_circ_125790,RMVar_hsa_circ_182100,RMVar_hsa_circ_346832,RMVar_hsa_circ_328632,RMVar_hsa_circ_182101,RMVar_hsa_circ_27760 46205 RMVar_ID_46205 Human_SNP_ID_617077055 A-to-I Human chr17 + 9873780 9873780 9873780 ATTGAAAGAACACATGCTAATGAATAAGCATTAGTTAATCAACTCTATTGCACTCTGCAGAAAGA ATTGAAAGAACACATGCTAATGAATAAGCATTCGTTAATCAACTCTATTGCACTCTGCAGAAAGA A C GLP2R Ensembl:ENSG00000065325 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs577204199 Functional Loss SNV dbSNP153 33..33 33 - - - 46206 RMVar_ID_46206 Human_SNP_ID_617077063 A-to-I Human chr17 + 9873819 9873819 9873819 CAACTCTATTGCACTCTGCAGAAAGAACTAGTAAACAGAAAGGTGGCCAACGAAAATGGCAGGGA CAACTCTATTGCACTCTGCAGAAAGAACTAGTGAACAGAAAGGTGGCCAACGAAAATGGCAGGGA A G GLP2R Ensembl:ENSG00000065325 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1344480380 Functional Loss SNV dbSNP153 33..33 33 - - - 46207 RMVar_ID_46207 Human_SNP_ID_617081567 A-to-I Human chr17 + 9891545 9891545 9891545 ATGAGGGACTTTTAATGTGAATTTTTATTTTTAGACAATTGCATTAAAATGTTATTTATATTGAC ATGAGGGACTTTTAATGTGAATTTTTATTTTTGGACAATTGCATTAAAATGTTATTTATATTGAC A G GLP2R Ensembl:ENSG00000065325 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs950291296 Functional Loss SNV dbSNP153 33..33 33 - - - 46208 RMVar_ID_46208 Human_SNP_ID_617152636 A-to-I Human chr17 - 10159924 10159924 10159924 AAAATTAGCTAGGTGTGGTGGCATGCACCTGTAGTCCCAGCTACTCAGGAGACTGAGGTGGGAGG AAAATTAGCTAGGTGTGGTGGCATGCACCTGTTGTCCCAGCTACTCAGGAGACTGAGGTGGGAGG T A GAS7 Ensembl:ENSG00000007237 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs207476283 Functional Loss SNV dbSNP153 33..33 33 - - - 46209 RMVar_ID_46209 Human_SNP_ID_617285338 A-to-I Human chr17 - 10673197 10673197 10673197 GAGATCGAGATCATCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAATTACAAAAATCAGCT GAGATCGAGATCATCCTGGCCAACATGGTGAATCCCCATCTCTACTAAAATTACAAAAATCAGCT T A SCO1 Ensembl:ENSG00000133028 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1011472164 Functional Loss SNV dbSNP153 33..33 33 - - - 46210 RMVar_ID_46210 Human_SNP_ID_617285339 A-to-I Human chr17 - 10673197 10673197 10673197 GAGATCGAGATCATCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAATTACAAAAATCAGCT GAGATCGAGATCATCCTGGCCAACATGGTGAAGCCCCATCTCTACTAAAATTACAAAAATCAGCT T C SCO1 Ensembl:ENSG00000133028 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1011472164 Functional Loss SNV dbSNP153 33..33 33 - - - 46211 RMVar_ID_46211 Human_SNP_ID_617285636 A-to-I Human chr17 - 10674246 10674242 10674246 GCGTGCATGGTAATTTTTGTATTTTTAGTAGAAACAGGATCTCGCCATGTTGGCCAGGCTGGTCT GCGTGCATGGTAATTTTTGTATTTTTAGTAGA____GGATCTCGCCATGTTGGCCAGGCTGGTCT CTGTT C SCO1 Ensembl:ENSG00000133028 Protein coding 3'UTR GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs199777858 Functional Loss DEL dbSNP153 33..36 33 - - - 46212 RMVar_ID_46212 Human_SNP_ID_617285637 A-to-I Human chr17 - 10674252 10674252 10674252 CCGGTGGCGTGCATGGTAATTTTTGTATTTTTAGTAGAAACAGGATCTCGCCATGTTGGCCAGGC CCGGTGGCGTGCATGGTAATTTTTGTATTTTTGGTAGAAACAGGATCTCGCCATGTTGGCCAGGC T C SCO1 Ensembl:ENSG00000133028 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031022686 Functional Loss SNV dbSNP153 33..33 33 - - - 46213 RMVar_ID_46213 Human_SNP_ID_617286140 A-to-I Human chr17 - 10676189 10676189 10676189 TACTCGGGAGGCTGAGGTAGGAGAATCGTGTGAATCTGGGAGGCGGAGGTTGCAGTGAGCCGAGA TACTCGGGAGGCTGAGGTAGGAGAATCGTGTGGATCTGGGAGGCGGAGGTTGCAGTGAGCCGAGA T C SCO1 Ensembl:ENSG00000133028 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1567571052 Functional Loss SNV dbSNP153 33..33 33 - - - 46214 RMVar_ID_46214 Human_SNP_ID_617286195 A-to-I Human chr17 - 10676346 10676346 10676346 TGGCTCATGCCTGTAATCCCAGTACTTTGGGAAGCAAAGGCGGGTGGATCACCTGAGGTTGAGAG TGGCTCATGCCTGTAATCCCAGTACTTTGGGAGGCAAAGGCGGGTGGATCACCTGAGGTTGAGAG T C SCO1 Ensembl:ENSG00000133028 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs541600963 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12882876 46215 RMVar_ID_46215 Human_SNP_ID_617286918 A-to-I Human chr17 - 10679038 10679038 10679038 CGGAGGCTGAGGCAGGAGAATCGCTTGAACCCAGGAGGCAGAGGTGGCAGTGAGGCAAGATTGCG CGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGGGAGGCAGAGGTGGCAGTGAGGCAAGATTGCG T C SCO1 Ensembl:ENSG00000133028 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs963202096 Functional Loss SNV dbSNP153 33..33 33 - - - 46216 RMVar_ID_46216 Human_SNP_ID_617286936 A-to-I Human chr17 - 10679102 10679102 10679102 CTCTCTCCTAAAAATACAAAAATTAGCCGGGCATGGTAGCGGGTGCCTGTAATCTCAGTTACTCC CTCTCTCCTAAAAATACAAAAATTAGCCGGGCGTGGTAGCGGGTGCCTGTAATCTCAGTTACTCC T C SCO1 Ensembl:ENSG00000133028 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs541403971 Functional Loss SNV dbSNP153 33..33 33 - - - 46217 RMVar_ID_46217 Human_SNP_ID_617286978 A-to-I Human chr17 - 10679221 10679221 10679221 TAGATTAGCTGGGCACAGTGGCTTATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGTGCAG TAGATTAGCTGGGCACAGTGGCTTATGCCTGTGATCCCAGCACTTTGGGAGGCCGAGGCGTGCAG T C SCO1 Ensembl:ENSG00000133028 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1301051282 Functional Loss SNV dbSNP153 33..33 33 - - - 46218 RMVar_ID_46218 Human_SNP_ID_617287134 A-to-I Human chr17 - 10679878 10679878 10679878 CCTGGCTACTCAGGAGACTGAAATGGAGTATCACTTGAGCCCAGGAATTCAAGGCTTCAGTGAGC CCTGGCTACTCAGGAGACTGAAATGGAGTATCGCTTGAGCCCAGGAATTCAAGGCTTCAGTGAGC T C SCO1 Ensembl:ENSG00000133028 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1033710893 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8812980,Human_RBP_ID_23710284 46219 RMVar_ID_46219 Human_SNP_ID_617287198 A-to-I Human chr17 - 10680000 10680000 10680000 AGGGCCTGAGGATTGCTAGAGGTTAGGTATTCAAGACAAGCCTGGGCAACATAGTGAGACCCCCC AGGGCCTGAGGATTGCTAGAGGTTAGGTATTCGAGACAAGCCTGGGCAACATAGTGAGACCCCCC T C SCO1 Ensembl:ENSG00000133028 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1304455678 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12882943 46220 RMVar_ID_46220 Human_SNP_ID_617287213 A-to-I Human chr17 - 10680056 10680056 10680056 AAATAACTTGCCTGGCACAATGGCTAATGCCTATAATCCCAAAACTTTGGGAGGCCAGGGCCTGA AAATAACTTGCCTGGCACAATGGCTAATGCCTGTAATCCCAAAACTTTGGGAGGCCAGGGCCTGA T C SCO1 Ensembl:ENSG00000133028 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs536325803 Functional Loss SNV dbSNP153 33..33 33 - - - 46221 RMVar_ID_46221 Human_SNP_ID_617782181 A-to-I Human chr17 + 12634163 12634163 12634163 AAAATTGGCTGGGCATGGTGGTGTGTGCCTGTAGTTCCAGCTACTCAGGAGGCCAAAGTTGGAGC AAAATTGGCTGGGCATGGTGGTGTGTGCCTGTCGTTCCAGCTACTCAGGAGGCCAAAGTTGGAGC A C LINC00670 Ensembl:ENSG00000179136 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs564876905 Functional Loss SNV dbSNP153 33..33 33 - - - 46222 RMVar_ID_46222 Human_SNP_ID_617782182 A-to-I Human chr17 + 12634163 12634163 12634163 AAAATTGGCTGGGCATGGTGGTGTGTGCCTGTAGTTCCAGCTACTCAGGAGGCCAAAGTTGGAGC AAAATTGGCTGGGCATGGTGGTGTGTGCCTGTTGTTCCAGCTACTCAGGAGGCCAAAGTTGGAGC A T LINC00670 Ensembl:ENSG00000179136 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs564876905 Functional Loss SNV dbSNP153 33..33 33 - - - 46223 RMVar_ID_46223 Human_SNP_ID_617826900 A-to-I Human chr17 + 12813662 12813662 12813662 CAAAAAACCAGCTTGAGAGATGGATGCTCAGTAACAGGAATGGATGTGTGACTTGGCACGTCCCC CAAAAAACCAGCTTGAGAGATGGATGCTCAGTTACAGGAATGGATGTGTGACTTGGCACGTCCCC A T ARHGAP44 Ensembl:ENSG00000006740 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs919847418 Functional Loss SNV dbSNP153 33..33 33 - - - 46224 RMVar_ID_46224 Human_SNP_ID_617860001 A-to-I Human chr17 + 12946637 12946637 12946637 CCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCTGGGCATAGTGGCAC CCTGGCCAACATGGTGAAACCCCGTCTCTACTTAAAATACAAAAATTAGCTGGGCATAGTGGCAC A T ARHGAP44 Ensembl:ENSG00000006740 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs987690769 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_182176,RMVar_hsa_circ_46221,RMVar_hsa_circ_336808,RMVar_hsa_circ_41723,RMVar_hsa_circ_315550,RMVar_hsa_circ_289348 46225 RMVar_ID_46225 Human_SNP_ID_617860005 A-to-I Human chr17 + 12946646 12946646 12946646 CATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCTGGGCATAGTGGCACACGCATCTG CATGGTGAAACCCCGTCTCTACTAAAAATACAGAAATTAGCTGGGCATAGTGGCACACGCATCTG A G ARHGAP44 Ensembl:ENSG00000006740 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1005956273 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_182176,RMVar_hsa_circ_46221,RMVar_hsa_circ_336808,RMVar_hsa_circ_41723,RMVar_hsa_circ_315550,RMVar_hsa_circ_289348 46226 RMVar_ID_46226 Human_SNP_ID_617869511 A-to-I Human chr17 + 12981956 12981956 12981956 TTGCTTGAACCTGGGAGGTGGAGGTTGCACTGAGCCAAGATCGTGCCACTGCCTTCCAGCTTGGG TTGCTTGAACCTGGGAGGTGGAGGTTGCACTGTGCCAAGATCGTGCCACTGCCTTCCAGCTTGGG A T ARHGAP44 Ensembl:ENSG00000006740 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs527249392 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_30002 46227 RMVar_ID_46227 Human_SNP_ID_617872487 A-to-I Human chr17 - 12991284 12991284 12991284 GGTATATTATATCATCTATTTGAAAAGGATAAAATTTTAAACTTTGACTTTGCATGCATGGCCCA GGTATATTATATCATCTATTTGAAAAGGATAAGATTTTAAACTTTGACTTTGCATGCATGGCCCA T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs746523447 Functional Loss SNV dbSNP153 33..33 33 - - - 46228 RMVar_ID_46228 Human_SNP_ID_617872488 A-to-I Human chr17 - 12991284 12991284 12991284 GGTATATTATATCATCTATTTGAAAAGGATAAAATTTTAAACTTTGACTTTGCATGCATGGCCCA GGTATATTATATCATCTATTTGAAAAGGATAACATTTTAAACTTTGACTTTGCATGCATGGCCCA T G - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs746523447 Functional Loss SNV dbSNP153 33..33 33 - - - 46229 RMVar_ID_46229 Human_SNP_ID_617878559 A-to-I Human chr17 - 13009873 13009873 13009873 GTGATTCTCCTGCCTCAGCCTCCCAAGTAGCTAGGATTATAGGTGCGCGCCACCACACCCAGTTA GTGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTATAGGTGCGCGCCACCACACCCAGTTA T C ELAC2 Ensembl:ENSG00000006744 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1567765704 Functional Loss SNV dbSNP153 33..33 33 - - - 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_182181,RMVar_hsa_circ_23609 46230 RMVar_ID_46230 Human_SNP_ID_617878662 A-to-I Human chr17 - 13010118 13010118 13010118 GCCTGCAACAAGTATTACTACTGACCTTTCATAATTGTCATCACTTGTAGGTTTCAGAGTTTAGA GCCTGCAACAAGTATTACTACTGACCTTTCATGATTGTCATCACTTGTAGGTTTCAGAGTTTAGA T C ELAC2 Ensembl:ENSG00000006744 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1203874658 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12888065 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_182181,RMVar_hsa_circ_23609 46231 RMVar_ID_46231 Human_SNP_ID_617878738 A-to-I Human chr17 - 13010350 13010350 13010350 CCTGACCAACGTGGTGAAACCCTGTCTGTACTAAAAATACAAAAATTAGCTGGGTGTGGTGGCGC CCTGACCAACGTGGTGAAACCCTGTCTGTACTGAAAATACAAAAATTAGCTGGGTGTGGTGGCGC T C ELAC2 Ensembl:ENSG00000006744 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1199725215 Functional Loss SNV dbSNP153 33..33 33 - - - 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_182181,RMVar_hsa_circ_23609 46232 RMVar_ID_46232 Human_SNP_ID_618187900 A-to-I Human chr17 + 14202324 14202324 14202324 ATAGTTCAATGCAGCCTAGAACTCCCAGGCTCAAGCGATCCTCCCTCCTCAGACTCCCAAGTAGG ATAGTTCAATGCAGCCTAGAACTCCCAGGCTCGAGCGATCCTCCCTCCTCAGACTCCCAAGTAGG A G COX10 Ensembl:ENSG00000006695 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1217782330 Functional Loss SNV dbSNP153 33..33 33 - - - 46233 RMVar_ID_46233 Human_SNP_ID_460782697 A-to-I Human chr11 + 30328394 30328394 30328394 GCATCAAGTGATCAACCCACATTGGCCTCCCAAAGTGCTGGGATTACAGGCAGGAGCCACAATGC GCATCAAGTGATCAACCCACATTGGCCTCCCAGAGTGCTGGGATTACAGGCAGGAGCCACAATGC A G ARL14EP Ensembl:ENSG00000152219 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs909415396 Functional Loss SNV dbSNP153 33..33 33 - - - 46234 RMVar_ID_46234 Human_SNP_ID_460966469 A-to-I Human chr11 - 31081510 31081510 31081510 CGCCTCCTGGGTTCAAGCGATTCTCCTGTCTCAGCCTCCCGAGTAGCTGGGATTGCGGGCATGTG CGCCTCCTGGGTTCAAGCGATTCTCCTGTCTCCGCCTCCCGAGTAGCTGGGATTGCGGGCATGTG T G DCDC1 Ensembl:ENSG00000170959 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1188751042 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_328762,RMVar_hsa_circ_344911,RMVar_hsa_circ_332125,RMVar_hsa_circ_66958,RMVar_hsa_circ_311298,RMVar_hsa_circ_37687,RMVar_hsa_circ_148841,RMVar_hsa_circ_148842,RMVar_hsa_circ_148843,RMVar_hsa_circ_32451,RMVar_hsa_circ_148844,RMVar_hsa_circ_345943,RMVar_hsa_circ_148845 46235 RMVar_ID_46235 Human_SNP_ID_461048028 A-to-I Human chr11 + 31431051 31431047 31431051 ATTTTAATTTCTTTTTTCTAAGACAGAGTCTCACTCTGTCGCGCCAGCTGGAGTGCAGTGCCATG ATTTTAATTTCTTTTTTCTAAGACAGAGT____CTCTGTCGCGCCAGCTGGAGTGCAGTGCCATG TCTCA T DNAJC24 Ensembl:ENSG00000170946 Protein coding 3'UTR GSE47997;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1564960630 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_24459536,Human_RBP_ID_26403238 46236 RMVar_ID_46236 Human_SNP_ID_461048056 A-to-I Human chr11 + 31431131 31431131 31431131 AACCTCCGTCTCCTGGGTTCAAGTGATTCTCCAGCCTCAGCCTCCCGAATAGCTGGGATTACACG AACCTCCGTCTCCTGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCGAATAGCTGGGATTACACG A T DNAJC24 Ensembl:ENSG00000170946 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs372884362 Functional Loss SNV dbSNP153 33..33 33 - - - 46237 RMVar_ID_46237 Human_SNP_ID_461048086 A-to-I Human chr11 + 31431288 31431288 31431288 GTGATCCACCTGCCTCGACCTCCCAAAGTGCTAGGATTACAGGTTTGAGCCACCGTGCCTGGCCT GTGATCCACCTGCCTCGACCTCCCAAAGTGCTGGGATTACAGGTTTGAGCCACCGTGCCTGGCCT A G DNAJC24 Ensembl:ENSG00000170946 Protein coding 3'UTR GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line - 29129909,29796672,31158229 RNA-Seq:(High) rs1247178758 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26409290 46238 RMVar_ID_46238 Human_SNP_ID_461048098 A-to-I Human chr11 + 31431360 31431360 31431360 GTTAATAGAGATGGGATTTCATCATGTTGGCTAGGCTGGTCTTGAACTCCTGGCCTCAAATGATC GTTAATAGAGATGGGATTTCATCATGTTGGCTGGGCTGGTCTTGAACTCCTGGCCTCAAATGATC A G DNAJC24 Ensembl:ENSG00000170946 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984436825 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26408304 46239 RMVar_ID_46239 Human_SNP_ID_461048148 A-to-I Human chr11 + 31431538 31431538 31431538 TTTGGAGTGTTGATATAATATTGGGGCCAGGCATGGTGGCTCACATCTGTAATCCCAGCACTTTG TTTGGAGTGTTGATATAATATTGGGGCCAGGCGTGGTGGCTCACATCTGTAATCCCAGCACTTTG A G DNAJC24 Ensembl:ENSG00000170946 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1195525270 Functional Loss SNV dbSNP153 33..33 33 - - - 46240 RMVar_ID_46240 Human_SNP_ID_461048151 A-to-I Human chr11 + 31431550 31431550 31431550 ATATAATATTGGGGCCAGGCATGGTGGCTCACATCTGTAATCCCAGCACTTTGGGAGACTAAGGC ATATAATATTGGGGCCAGGCATGGTGGCTCACTTCTGTAATCCCAGCACTTTGGGAGACTAAGGC A T DNAJC24 Ensembl:ENSG00000170946 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1037856041 Functional Loss SNV dbSNP153 33..33 33 - - - 46241 RMVar_ID_46241 Human_SNP_ID_461048167 A-to-I Human chr11 + 31431641 31431640 31431641 CAAGACCACCCTGGCCAACATGGTGAAACCCCATATCTACTAAAAATAATTTTTTTAAAAATTAG CAAGACCACCCTGGCCAACATGGTGAAACCCC_TATCTACTAAAAATAATTTTTTTAAAAATTAG CA C DNAJC24 Ensembl:ENSG00000170946 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs959257019 Functional Loss DEL dbSNP153 33..33 33 - - - Human_miRNA_ID_455386,Human_miRNA_ID_457347 46242 RMVar_ID_46242 Human_SNP_ID_461048168 A-to-I Human chr11 + 31431641 31431641 31431641 CAAGACCACCCTGGCCAACATGGTGAAACCCCATATCTACTAAAAATAATTTTTTTAAAAATTAG CAAGACCACCCTGGCCAACATGGTGAAACCCCGTATCTACTAAAAATAATTTTTTTAAAAATTAG A G DNAJC24 Ensembl:ENSG00000170946 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1012202357 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_455386,Human_miRNA_ID_457347 46243 RMVar_ID_46243 Human_SNP_ID_461054686 A-to-I Human chr11 + 31460639 31460639 31460639 ATCCATGACAGAAATTTACCTTTGGATACCATAAAAATGTCGACTAAGATTTTCTGCAAAGACAA ATCCATGACAGAAATTTACCTTTGGATACCATGAAAATGTCGACTAAGATTTTCTGCAAAGACAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs374734567 Functional Loss SNV dbSNP153 33..33 33 - - - 46244 RMVar_ID_46244 Human_SNP_ID_461054687 A-to-I Human chr11 + 31460639 31460639 31460639 ATCCATGACAGAAATTTACCTTTGGATACCATAAAAATGTCGACTAAGATTTTCTGCAAAGACAA ATCCATGACAGAAATTTACCTTTGGATACCATTAAAATGTCGACTAAGATTTTCTGCAAAGACAA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs374734567 Functional Loss SNV dbSNP153 33..33 33 - - - 46245 RMVar_ID_46245 Human_SNP_ID_461061010 A-to-I Human chr11 - 31488722 31488722 31488722 GGTCACAAGGTTTTTTTTACAGTATCACACACATTCCTTATATTCAGTACATATCTAATTTAGTC GGTCACAAGGTTTTTTTTACAGTATCACACACGTTCCTTATATTCAGTACATATCTAATTTAGTC T C IMMP1L Ensembl:ENSG00000148950 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs377020751 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3373636,Human_RBP_ID_9637307 46246 RMVar_ID_46246 Human_SNP_ID_461068026 A-to-I Human chr11 + 31516692 31516692 31516692 TTTTGTATTTTTTGTAGAGATGGAGTTTTGCCATTTTGTCCAGGCTTGTCTCAAACTCTTGAGCT TTTTGTATTTTTTGTAGAGATGGAGTTTTGCCGTTTTGTCCAGGCTTGTCTCAAACTCTTGAGCT A G ELP4 Ensembl:ENSG00000109911 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1479371259 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107838,RMVar_hsa_circ_148849 46247 RMVar_ID_46247 Human_SNP_ID_461108602 A-to-I Human chr11 + 31681844 31681844 31681844 GCTCACGGCAACCTCGCCTCCTGGGTTCAAGCAATTCTCCCGCCTCAGCCTCCCTAGTAGCTGGG GCTCACGGCAACCTCGCCTCCTGGGTTCAAGCGATTCTCCCGCCTCAGCCTCCCTAGTAGCTGGG A G ELP4 Ensembl:ENSG00000109911 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1413350718 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1223912 46248 RMVar_ID_46248 Human_SNP_ID_461117337 A-to-I Human chr11 + 31717997 31717997 31717997 CACCCTTTCTTTAATGGACCCGGGGTCTCACTATGTTGCACAGGCTGGTCTCAAACTCCTCAACT CACCCTTTCTTTAATGGACCCGGGGTCTCACTGTGTTGCACAGGCTGGTCTCAAACTCCTCAACT A G ELP4 Ensembl:ENSG00000109911 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1468720980 Functional Loss SNV dbSNP153 33..33 33 - - - 46249 RMVar_ID_46249 Human_SNP_ID_461212964 A-to-I Human chr11 + 32091369 32091369 32091369 GCGGCCCCCTGAGGACAACCAGAGCTTCCAGTACGACCACGAGGCCTTCCTGGGCAAGGAGGACT GCGGCCCCCTGAGGACAACCAGAGCTTCCAGTGCGACCACGAGGCCTTCCTGGGCAAGGAGGACT A G RCN1,AL035078.4 Ensembl:ENSG00000049449,Ensembl:ENSG00000285283 Protein coding,Protein coding CDS,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1317206785 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4157765,Human_RBP_ID_22754626 Human_Splice_Rec_1225489 46250 RMVar_ID_46250 Human_SNP_ID_461212968 A-to-I Human chr11 + 32091375 32091375 32091375 CCCTGAGGACAACCAGAGCTTCCAGTACGACCACGAGGCCTTCCTGGGCAAGGAGGACTCCAAGA CCCTGAGGACAACCAGAGCTTCCAGTACGACCCCGAGGCCTTCCTGGGCAAGGAGGACTCCAAGA A C RCN1,AL035078.4 Ensembl:ENSG00000049449,Ensembl:ENSG00000285283 Protein coding,Protein coding CDS,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350733824 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4189876,Human_RBP_ID_22754626 Human_Splice_Rec_1225489 46251 RMVar_ID_46251 Human_SNP_ID_461398578 A-to-I Human chr11 + 32856997 32856997 32856997 GGGACCACAGGTGCACCTCGGTACACCTGGCTAATTTTTGTGTTTTTTGTAGAGACAGGGTTTCA GGGACCACAGGTGCACCTCGGTACACCTGGCTTATTTTTGTGTTTTTTGTAGAGACAGGGTTTCA A T PRRG4 Ensembl:ENSG00000135378 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs556932866 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1626032,Human_miRNA_ID_1666531 RMVar_hsa_circ_117764,RMVar_hsa_circ_115469,RMVar_hsa_circ_148870,RMVar_hsa_circ_86171,RMVar_hsa_circ_148871,RMVar_hsa_circ_148872 46252 RMVar_ID_46252 Human_SNP_ID_461398581 A-to-I Human chr11 + 32857021 32857021 32857021 ACCTGGCTAATTTTTGTGTTTTTTGTAGAGACAGGGTTTCACCATGTTGCCCATGCTGGTCTCTA ACCTGGCTAATTTTTGTGTTTTTTGTAGAGACGGGGTTTCACCATGTTGCCCATGCTGGTCTCTA A G PRRG4 Ensembl:ENSG00000135378 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs544272100 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_975258,Human_miRNA_ID_1950642,Human_miRNA_ID_1951929,Human_miRNA_ID_2444084 RMVar_hsa_circ_117764,RMVar_hsa_circ_115469,RMVar_hsa_circ_148870,RMVar_hsa_circ_86171,RMVar_hsa_circ_148871,RMVar_hsa_circ_148872 46253 RMVar_ID_46253 Human_SNP_ID_461409044 A-to-I Human chr11 + 32898812 32898812 32898812 ACCAGGCTGGTCGGGAACTCTTGGCCTCAAGCAGTCTTCCTGCCTTGGCCTCTCAGGCGTGAGCC ACCAGGCTGGTCGGGAACTCTTGGCCTCAAGCTGTCTTCCTGCCTTGGCCTCTCAGGCGTGAGCC A T QSER1 Ensembl:ENSG00000060749 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1341172148 Functional Loss SNV dbSNP153 33..33 33 - - - 46254 RMVar_ID_46254 Human_SNP_ID_461409673 A-to-I Human chr11 + 32901828 32901828 32901828 GGGAATGGCCAGGCGTGGTGGCTTGTGCCCATAATCCCAGCACTTTGGGATGCTGAGATGGGCTG GGGAATGGCCAGGCGTGGTGGCTTGTGCCCATCATCCCAGCACTTTGGGATGCTGAGATGGGCTG A C QSER1 Ensembl:ENSG00000060749 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs949461981 Functional Loss SNV dbSNP153 33..33 33 - - - 46255 RMVar_ID_46255 Human_SNP_ID_461410757 A-to-I Human chr11 + 32906412 32906412 32906412 GCCACTGCACTCCAGCCAGGGCAACAAGAGCAAAACTCCGTTTTTTAAGAGACAGGGTCTTACTC GCCACTGCACTCCAGCCAGGGCAACAAGAGCAGAACTCCGTTTTTTAAGAGACAGGGTCTTACTC A G QSER1 Ensembl:ENSG00000060749 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1192992568 Functional Loss SNV dbSNP153 33..33 33 - - - 46256 RMVar_ID_46256 Human_SNP_ID_461410808 A-to-I Human chr11 + 32906614 32906614 32906614 GTTTTTGTTCATTGTAGAGATGGGGTCTTGCTATTTTCTCAGGGTGGTCTCAAACTTCTGGGCTC GTTTTTGTTCATTGTAGAGATGGGGTCTTGCTGTTTTCTCAGGGTGGTCTCAAACTTCTGGGCTC A G QSER1 Ensembl:ENSG00000060749 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs961450158 Functional Loss SNV dbSNP153 33..33 33 - - - 46257 RMVar_ID_46257 Human_SNP_ID_461412126 A-to-I Human chr11 + 32912758 32912758 32912758 TAGGGAGACCTTGTCTCTATAAAAAGATATTTAAAAAACTGGCCAGACATGGTGTCGCACGTCTT TAGGGAGACCTTGTCTCTATAAAAAGATATTTTAAAAACTGGCCAGACATGGTGTCGCACGTCTT A T QSER1 Ensembl:ENSG00000060749 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1206056418 Functional Loss SNV dbSNP153 33..33 33 - - - 46258 RMVar_ID_46258 Human_SNP_ID_461412324 A-to-I Human chr11 + 32913400 32913400 32913400 TTATTTTAGTAGAGACGAGGTTTCATCGTGTTAGCCAGGATGGTCTCGATCTCTTGACCTCATGA TTATTTTAGTAGAGACGAGGTTTCATCGTGTTGGCCAGGATGGTCTCGATCTCTTGACCTCATGA A G QSER1 Ensembl:ENSG00000060749 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1471024004 Functional Loss SNV dbSNP153 33..33 33 - - - 46259 RMVar_ID_46259 Human_SNP_ID_461414334 A-to-I Human chr11 + 32922650 32922650 32922650 AGAATTACAGACCTGTGCCACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTTG AGAATTACAGACCTGTGCCACCATGCCTGGCTGATTTTTGTATTTTTAGTAGAGATGGGGTTTTG A G QSER1 Ensembl:ENSG00000060749 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1262486136 Functional Loss SNV dbSNP153 33..33 33 - - - 46260 RMVar_ID_46260 Human_SNP_ID_461414720 A-to-I Human chr11 + 32924331 32924331 32924331 CACACCTGTAATCCTAGCACTTTGGGAGTCCAAAGTGGGTAGATTGCTTGTTTGAGTCCAGGAGT CACACCTGTAATCCTAGCACTTTGGGAGTCCACAGTGGGTAGATTGCTTGTTTGAGTCCAGGAGT A C QSER1 Ensembl:ENSG00000060749 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1370739427 Functional Loss SNV dbSNP153 33..33 33 - - - 46261 RMVar_ID_46261 Human_SNP_ID_461414736 A-to-I Human chr11 + 32924437 32924437 32924437 AAAAAGTTAGCTGGTGGTGGTGGTGCACGCCTATGGTCCCAGCTACTCGAGAGACTGAGGTGAGA AAAAAGTTAGCTGGTGGTGGTGGTGCACGCCTGTGGTCCCAGCTACTCGAGAGACTGAGGTGAGA A G QSER1 Ensembl:ENSG00000060749 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs894793460 Functional Loss SNV dbSNP153 33..33 33 - - - 46262 RMVar_ID_46262 Human_SNP_ID_461414741 A-to-I Human chr11 + 32924449 32924449 32924449 GGTGGTGGTGGTGCACGCCTATGGTCCCAGCTACTCGAGAGACTGAGGTGAGAGAATCACCTGAG GGTGGTGGTGGTGCACGCCTATGGTCCCAGCTGCTCGAGAGACTGAGGTGAGAGAATCACCTGAG A G QSER1 Ensembl:ENSG00000060749 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1226353488 Functional Loss SNV dbSNP153 33..33 33 - - - 46263 RMVar_ID_46263 Human_SNP_ID_461422754 A-to-I Human chr11 + 32958457 32958457 32958457 TCGCCCAGGCTGAAGTGCAATGGCATGATCCTAGCTCACTGCAGCCTCGAACACCTGGGCTCGTA TCGCCCAGGCTGAAGTGCAATGGCATGATCCTGGCTCACTGCAGCCTCGAACACCTGGGCTCGTA A G QSER1 Ensembl:ENSG00000060749 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1472001843 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11600377 RMVar_hsa_circ_73669,RMVar_hsa_circ_348166,RMVar_hsa_circ_358501,RMVar_hsa_circ_19227,RMVar_hsa_circ_80078,RMVar_hsa_circ_83804,RMVar_hsa_circ_22148,RMVar_hsa_circ_355741,RMVar_hsa_circ_148881,RMVar_hsa_circ_148882,RMVar_hsa_circ_284132,RMVar_hsa_circ_24035,RMVar_hsa_circ_148885,RMVar_hsa_circ_66338,RMVar_hsa_circ_148884,RMVar_hsa_circ_109426,RMVar_hsa_circ_148886 46264 RMVar_ID_46264 Human_SNP_ID_461438531 A-to-I Human chr11 + 33029242 33029242 33029242 CAATAAGGCCGGGTGCGGTGGCCCATGCCTGTAATCCTAGCACTTTGGGAGGCTGAGGTGGGTGG CAATAAGGCCGGGTGCGGTGGCCCATGCCTGTCATCCTAGCACTTTGGGAGGCTGAGGTGGGTGG A C DEPDC7 Ensembl:ENSG00000121690 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1226691900 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_148889,RMVar_hsa_circ_81878 46265 RMVar_ID_46265 Human_SNP_ID_461438887 A-to-I Human chr11 + 33030683 33030682 33030683 TTGGCTCACTGCAGCCTCTGCCTCCTGGGTTCAAGCAATTCTCCCACCTCAGCCTCCCAAGTATC TTGGCTCACTGCAGCCTCTGCCTCCTGGGTTC_AGCAATTCTCCCACCTCAGCCTCCCAAGTATC CA C DEPDC7 Ensembl:ENSG00000121690 Protein coding intron GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs573030797 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_148889,RMVar_hsa_circ_81878 46266 RMVar_ID_46266 Human_SNP_ID_461441826 A-to-I Human chr11 + 33040796 33040796 33040796 ACCTCCTCTCCCCCTCCTCTCCCCCTCCAGACATGTTTTAACTAGGTGAAATCCTACTCCTTTTA ACCTCCTCTCCCCCTCCTCTCCCCCTCCAGACCTGTTTTAACTAGGTGAAATCCTACTCCTTTTA A C TCP11L1 Ensembl:ENSG00000176148 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11032112 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5531,GWAS_ID_5532,GWAS_ID_5533,GWAS_ID_5534,GWAS_ID_5535,GWAS_ID_5536,GWAS_ID_5537,GWAS_ID_5538,GWAS_ID_5539,GWAS_ID_5540,GWAS_ID_5541,GWAS_ID_5542,GWAS_ID_5543,GWAS_ID_5544,GWAS_ID_5545,GWAS_ID_5546,GWAS_ID_5547 46267 RMVar_ID_46267 Human_SNP_ID_461441827 A-to-I Human chr11 + 33040796 33040796 33040796 ACCTCCTCTCCCCCTCCTCTCCCCCTCCAGACATGTTTTAACTAGGTGAAATCCTACTCCTTTTA ACCTCCTCTCCCCCTCCTCTCCCCCTCCAGACGTGTTTTAACTAGGTGAAATCCTACTCCTTTTA A G TCP11L1 Ensembl:ENSG00000176148 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11032112 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5531,GWAS_ID_5532,GWAS_ID_5533,GWAS_ID_5534,GWAS_ID_5535,GWAS_ID_5536,GWAS_ID_5537,GWAS_ID_5538,GWAS_ID_5539,GWAS_ID_5540,GWAS_ID_5541,GWAS_ID_5542,GWAS_ID_5543,GWAS_ID_5544,GWAS_ID_5545,GWAS_ID_5546,GWAS_ID_5547 46268 RMVar_ID_46268 Human_SNP_ID_461442031 A-to-I Human chr11 + 33041628 33041628 33041628 CGAAAATTAGCGAGGCGTGGTGGTGGGCGCCTATAATCCCAGCTACTGGGGAGGCTGAGGCAGAA CGAAAATTAGCGAGGCGTGGTGGTGGGCGCCTGTAATCCCAGCTACTGGGGAGGCTGAGGCAGAA A G TCP11L1 Ensembl:ENSG00000176148 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4460781 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5548,GWAS_ID_5549,GWAS_ID_5550,GWAS_ID_5551,GWAS_ID_5552,GWAS_ID_5553,GWAS_ID_5554,GWAS_ID_5555,GWAS_ID_5556,GWAS_ID_5557,GWAS_ID_5558,GWAS_ID_5559,GWAS_ID_5560,GWAS_ID_5561,GWAS_ID_5562,GWAS_ID_5563,GWAS_ID_5564,GWAS_ID_5565,GWAS_ID_5566,GWAS_ID_5567,GWAS_ID_5568,GWAS_ID_5569,GWAS_ID_5570,GWAS_ID_5571,GWAS_ID_5572,GWAS_ID_5573,GWAS_ID_5574,GWAS_ID_5575,GWAS_ID_5576,GWAS_ID_5577,GWAS_ID_5578,GWAS_ID_5579,GWAS_ID_5580,GWAS_ID_5581,GWAS_ID_5582,GWAS_ID_5583,GWAS_ID_5584,GWAS_ID_5585,GWAS_ID_5586,GWAS_ID_5587,GWAS_ID_5588,GWAS_ID_5589,GWAS_ID_5590,GWAS_ID_5591,GWAS_ID_5592,GWAS_ID_5593,GWAS_ID_5594,GWAS_ID_5595,GWAS_ID_5596,GWAS_ID_5597,GWAS_ID_5598,GWAS_ID_5599,GWAS_ID_5600,GWAS_ID_5601,GWAS_ID_5602,GWAS_ID_5603,GWAS_ID_5604,GWAS_ID_5605,GWAS_ID_5606,GWAS_ID_5607,GWAS_ID_5608,GWAS_ID_5609,GWAS_ID_5610,GWAS_ID_5611,GWAS_ID_5612,GWAS_ID_5613,GWAS_ID_5614,GWAS_ID_5615,GWAS_ID_5616,GWAS_ID_5617,GWAS_ID_5618,GWAS_ID_5619,GWAS_ID_5620,GWAS_ID_5621,GWAS_ID_5622,GWAS_ID_5623,GWAS_ID_5624,GWAS_ID_5625,GWAS_ID_5626,GWAS_ID_5627,GWAS_ID_5628,GWAS_ID_5629,GWAS_ID_5630,GWAS_ID_5631,GWAS_ID_5632,GWAS_ID_5633,GWAS_ID_5634,GWAS_ID_5635,GWAS_ID_5636,GWAS_ID_5637,GWAS_ID_5638,GWAS_ID_5639,GWAS_ID_5640,GWAS_ID_5641,GWAS_ID_5642,GWAS_ID_5643,GWAS_ID_5644,GWAS_ID_5645,GWAS_ID_5646,GWAS_ID_5647,GWAS_ID_5648,GWAS_ID_5649,GWAS_ID_5650,GWAS_ID_5651,GWAS_ID_5652,GWAS_ID_5653,GWAS_ID_5654,GWAS_ID_5655,GWAS_ID_5656,GWAS_ID_5657,GWAS_ID_5658,GWAS_ID_5659,GWAS_ID_5660,GWAS_ID_5661,GWAS_ID_5662,GWAS_ID_5663 46269 RMVar_ID_46269 Human_SNP_ID_461442426 A-to-I Human chr11 + 33043000 33043000 33043000 AGGCAGGAGAATCACTTGAAACCGGAAGGTGGAAGTTGCAGTAAACTGAGATCGCACCACTGCAT AGGCAGGAGAATCACTTGAAACCGGAAGGTGGTAGTTGCAGTAAACTGAGATCGCACCACTGCAT A T TCP11L1 Ensembl:ENSG00000176148 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1564972478 Functional Loss SNV dbSNP153 33..33 33 - - - 46270 RMVar_ID_46270 Human_SNP_ID_461442613 A-to-I Human chr11 + 33043871 33043871 33043871 GGAAGGCCTCGAAGATGCTGTGGAAGGTGCTGATGAAGCCTTACAAAAAGCAATAAAGTCAGACT GGAAGGCCTCGAAGATGCTGTGGAAGGTGCTGGTGAAGCCTTACAAAAAGCAATAAAGTCAGACT A G TCP11L1 Ensembl:ENSG00000176148 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs752285623 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8768976 Human_Splice_Rec_1226167,Human_Splice_Rec_1226175,Human_Splice_Rec_1226193,Human_Splice_Rec_1226217,Human_Splice_Rec_1226221,Human_Splice_Rec_1226241,Human_Splice_Rec_1226247,Human_Splice_Rec_1226265 RMVar_hsa_circ_51131,RMVar_hsa_circ_296161,RMVar_hsa_circ_304976,RMVar_hsa_circ_305994,RMVar_hsa_circ_296889,RMVar_hsa_circ_74062,RMVar_hsa_circ_148890,RMVar_hsa_circ_148891,RMVar_hsa_circ_148892 46271 RMVar_ID_46271 Human_SNP_ID_461447408 A-to-I Human chr11 + 33063085 33063085 33063085 AGGGGTCTCGCTATGTTACTCAGGCTGATCTTAAACTCCTGGCCTCAAGTGGTCCTCCCTCCTTG AGGGGTCTCGCTATGTTACTCAGGCTGATCTTGAACTCCTGGCCTCAAGTGGTCCTCCCTCCTTG A G TCP11L1 Ensembl:ENSG00000176148 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1007781749 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9298,RMVar_hsa_circ_51131,RMVar_hsa_circ_74062,RMVar_hsa_circ_22396,RMVar_hsa_circ_300671,RMVar_hsa_circ_329530,RMVar_hsa_circ_148897 46272 RMVar_ID_46272 Human_SNP_ID_461449439 A-to-I Human chr11 + 33071184 33071184 33071184 TAATAATACAAAAATTAGCTGGGCATGGTGGCATGCGCCTGTAATCCCAGCTACTCGGGAGGCAG TAATAATACAAAAATTAGCTGGGCATGGTGGCGTGCGCCTGTAATCCCAGCTACTCGGGAGGCAG A G TCP11L1 Ensembl:ENSG00000176148 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1205027131 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9298,RMVar_hsa_circ_51131,RMVar_hsa_circ_74062,RMVar_hsa_circ_22396,RMVar_hsa_circ_329530 46273 RMVar_ID_46273 Human_SNP_ID_461450148 A-to-I Human chr11 + 33073953 33073953 33073953 GAAACTTACAAGTTAGCCGGGCGTGGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCCGAG GAAACTTACAAGTTAGCCGGGCGTGGTGGCTCCCGCCTATAATCCCAGCACTTTGGGAGGCCGAG A C TCP11L1 Ensembl:ENSG00000176148 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1421559011 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9298,RMVar_hsa_circ_51131 46274 RMVar_ID_46274 Human_SNP_ID_461450152 A-to-I Human chr11 + 33073961 33073961 33073961 CAAGTTAGCCGGGCGTGGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCCGAGGCAGGCAG CAAGTTAGCCGGGCGTGGTGGCTCACGCCTATGATCCCAGCACTTTGGGAGGCCGAGGCAGGCAG A G TCP11L1 Ensembl:ENSG00000176148 Protein coding intron GSE38233;GSE100210;GSE107867;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 24183664,29129909,30559470,30559470 RNA-Seq:(High) rs1368334287 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9298,RMVar_hsa_circ_51131 46275 RMVar_ID_46275 Human_SNP_ID_461450292 A-to-I Human chr11 + 33074657 33074657 33074657 TTAAAAAAACAAAACAAAAAACAGGGCTGGGCATGGTGGCTTACACTATAATCCCAGTACTTTGG TTAAAAAAACAAAACAAAAAACAGGGCTGGGCTTGGTGGCTTACACTATAATCCCAGTACTTTGG A T TCP11L1 Ensembl:ENSG00000176148 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1373721685 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9298,RMVar_hsa_circ_51131 46276 RMVar_ID_46276 Human_SNP_ID_461450296 A-to-I Human chr11 + 33074672 33074672 33074672 AAAAAACAGGGCTGGGCATGGTGGCTTACACTATAATCCCAGTACTTTGGAATGCCAAGGCAGGA AAAAAACAGGGCTGGGCATGGTGGCTTACACTGTAATCCCAGTACTTTGGAATGCCAAGGCAGGA A G TCP11L1 Ensembl:ENSG00000176148 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1398164637 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9298,RMVar_hsa_circ_51131 46277 RMVar_ID_46277 Human_SNP_ID_461450395 A-to-I Human chr11 + 33075229 33075229 33075229 ACCCAAGCCTTTGGTTCATTTTTTATTTTTTCAAGACGGAGTCTTGCTCTGTCACCCAGGCTGGA ACCCAAGCCTTTGGTTCATTTTTTATTTTTTCCAGACGGAGTCTTGCTCTGTCACCCAGGCTGGA A C TCP11L1 Ensembl:ENSG00000176148 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1206961654 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4189955,Human_RBP_ID_6068842,Human_RBP_ID_11600992,Human_RBP_ID_26889804 RMVar_hsa_circ_9298,RMVar_hsa_circ_51131 46278 RMVar_ID_46278 Human_SNP_ID_461450407 A-to-I Human chr11 + 33075280 33075280 33075280 TCACCCAGGCTGGAGTGTGGTGGCGCGATCTCAGCTTACTGCAACCTCCATCTCCCGGTTTCAAG TCACCCAGGCTGGAGTGTGGTGGCGCGATCTCGGCTTACTGCAACCTCCATCTCCCGGTTTCAAG A G TCP11L1 Ensembl:ENSG00000176148 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1195925833 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9298,RMVar_hsa_circ_51131 46279 RMVar_ID_46279 Human_SNP_ID_461450435 A-to-I Human chr11 + 33075350 33075350 33075350 CTCCTGCCTCAGCCTCCTGAATAGCTGGGATTACAGGCACGCGCCACCATGCCCGGCTAATTTTT CTCCTGCCTCAGCCTCCTGAATAGCTGGGATTGCAGGCACGCGCCACCATGCCCGGCTAATTTTT A G TCP11L1 Ensembl:ENSG00000176148 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs763420813 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9298,RMVar_hsa_circ_51131 46280 RMVar_ID_46280 Human_SNP_ID_461450449 A-to-I Human chr11 + 33075394 33075394 33075394 CACCATGCCCGGCTAATTTTTGGATTCTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGG CACCATGCCCGGCTAATTTTTGGATTCTTAGTGGAGACGGGGTTTCACCATGTTGGCCAGGCTGG A G TCP11L1 Ensembl:ENSG00000176148 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs888675092 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9298,RMVar_hsa_circ_51131 46281 RMVar_ID_46281 Human_SNP_ID_461450455 A-to-I Human chr11 + 33075411 33075411 33075411 TTTTGGATTCTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCTTGACCT TTTTGGATTCTTAGTAGAGACGGGGTTTCACCGTGTTGGCCAGGCTGGTCTCGAACTCTTGACCT A G TCP11L1 Ensembl:ENSG00000176148 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs941515789 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9298,RMVar_hsa_circ_51131 46282 RMVar_ID_46282 Human_SNP_ID_461450862 A-to-I Human chr11 + 33076985 33076985 33076985 TGACCTCGTGATCCACCCGCCTTGGCCTCCCAAAGTGCTGGGATTGTAGGCGTGAGCCACTGCGC TGACCTCGTGATCCACCCGCCTTGGCCTCCCAGAGTGCTGGGATTGTAGGCGTGAGCCACTGCGC A G TCP11L1,LINC00294 Ensembl:ENSG00000176148,Ensembl:ENSG00000280798 Protein coding,lincRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1002878050 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9298,RMVar_hsa_circ_51131 46283 RMVar_ID_46283 Human_SNP_ID_461451600 A-to-I Human chr11 + 33080232 33080232 33080232 CAGGCTGGACAACACAGGTAGATCCTGTTTCTACATAAAATTTAAAAAATTAGCTGGGTATGGTG CAGGCTGGACAACACAGGTAGATCCTGTTTCTTCATAAAATTTAAAAAATTAGCTGGGTATGGTG A T TCP11L1 Ensembl:ENSG00000176148 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1449385676 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9298,RMVar_hsa_circ_51131 46284 RMVar_ID_46284 Human_SNP_ID_461462192 A-to-I Human chr11 - 33129012 33129012 33129012 AATTGCTTCTAAAATTTATTAACTTTTCCAGTATCTGTTGTGTAAATGCATGCCAGACACTGCAT AATTGCTTCTAAAATTTATTAACTTTTCCAGTGTCTGTTGTGTAAATGCATGCCAGACACTGCAT T C CSTF3 Ensembl:ENSG00000176102 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,cerebellum - 29129909,30559470 RNA-Seq:(High) rs572465889 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8350112 RMVar_hsa_circ_6480,RMVar_hsa_circ_39886 46285 RMVar_ID_46285 Human_SNP_ID_461462231 A-to-I Human chr11 - 33129212 33129212 33129212 TGGTGTGCACCTGTAACCCCAACTGCTTGGGAAGCTGAGGCAGGAGAATTACTTGAGCCCTGGAG TGGTGTGCACCTGTAACCCCAACTGCTTGGGATGCTGAGGCAGGAGAATTACTTGAGCCCTGGAG T A CSTF3 Ensembl:ENSG00000176102 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs563881976 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24916099 RMVar_hsa_circ_6480,RMVar_hsa_circ_39886 46286 RMVar_ID_46286 Human_SNP_ID_461463010 A-to-I Human chr11 - 33132470 33132470 33132470 GTAGTCCTAGCATTTGGGAGGCCAAGGTGGGCAGATTGCCTGAGCCCCACGAGTTTGAGACCAGC GTAGTCCTAGCATTTGGGAGGCCAAGGTGGGCGGATTGCCTGAGCCCCACGAGTTTGAGACCAGC T C CSTF3 Ensembl:ENSG00000176102 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs572955156 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6480,RMVar_hsa_circ_39886 46287 RMVar_ID_46287 Human_SNP_ID_461467720 A-to-I Human chr11 - 33152213 33152213 33152213 CTCTGTCGCCCAGGCTGGAGTGCAGCGGCACAATCTTGGCTCAGTGGAACCTCTGCCCCTCCCCG CTCTGTCGCCCAGGCTGGAGTGCAGCGGCACAGTCTTGGCTCAGTGGAACCTCTGCCCCTCCCCG T C CSTF3 Ensembl:ENSG00000176102 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1046585697 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11602348 RMVar_hsa_circ_99096,RMVar_hsa_circ_148913,RMVar_hsa_circ_148915 46288 RMVar_ID_46288 Human_SNP_ID_461467763 A-to-I Human chr11 - 33152402 33152402 33152402 AAACCCAGCCAGGTGCGGTGGTGCACGCCTGTAGTCCCAGCTATTTGGGAGGCTGAGGCAGGAGG AAACCCAGCCAGGTGCGGTGGTGCACGCCTGTGGTCCCAGCTATTTGGGAGGCTGAGGCAGGAGG T C CSTF3 Ensembl:ENSG00000176102 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1245683778 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99096,RMVar_hsa_circ_148913,RMVar_hsa_circ_148915 46289 RMVar_ID_46289 Human_SNP_ID_461469170 A-to-I Human chr11 - 33157714 33157714 33157714 TTGTAGAATAAACCTGATACTATCTTAAATTTATTACTAAAATATATGGATAGTCATTTTTCTCT TTGTAGAATAAACCTGATACTATCTTAAATTTGTTACTAAAATATATGGATAGTCATTTTTCTCT T C CSTF3 Ensembl:ENSG00000176102 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1454533554 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6069271,Human_RBP_ID_9638180,Human_RBP_ID_17795009 RMVar_hsa_circ_99096,RMVar_hsa_circ_148913,RMVar_hsa_circ_148915 46290 RMVar_ID_46290 Human_SNP_ID_461469171 A-to-I Human chr11 - 33157725 33157725 33157725 GAAGTTCAAGTTTGTAGAATAAACCTGATACTATCTTAAATTTATTACTAAAATATATGGATAGT GAAGTTCAAGTTTGTAGAATAAACCTGATACTGTCTTAAATTTATTACTAAAATATATGGATAGT T C CSTF3 Ensembl:ENSG00000176102 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs564998098 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2266832,Human_RBP_ID_6069271,Human_RBP_ID_9638180,Human_RBP_ID_17795009 RMVar_hsa_circ_99096,RMVar_hsa_circ_148913,RMVar_hsa_circ_148915 46291 RMVar_ID_46291 Human_SNP_ID_461469933 A-to-I Human chr11 + 33160895 33160895 33160895 TTAGCTTTGTCTCAAATATTTCTCAAACTAGTAACCTATTTCTGGGTACAGTATATTTGGCGGGG TTAGCTTTGTCTCAAATATTTCTCAAACTAGTTACCTATTTCTGGGTACAGTATATTTGGCGGGG A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256942511 Functional Loss SNV dbSNP153 33..33 33 - - - 46292 RMVar_ID_46292 Human_SNP_ID_461469949 A-to-I Human chr11 + 33160944 33160943 33160945 AGTATATTTGGCGGGGTAAAAGAAACACTGTCAAGTTTTTCTAAAACGTCGGGTGCACGTTAAAA AGTATATTTGGCGGGGTAAAAGAAACACTGTC__GTTTTTCTAAAACGTCGGGTGCACGTTAAAA CAA C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1043676633 Functional Loss DEL dbSNP153 33..34 33 - - - 46293 RMVar_ID_46293 Human_SNP_ID_461469957 A-to-I Human chr11 - 33161007 33161007 33161007 GGACTACTCCAGATGGGATGCTTTCCTTTGATATCGTTTTGGTATTAGAGTGGATAGGAATTATT GGACTACTCCAGATGGGATGCTTTCCTTTGATGTCGTTTTGGTATTAGAGTGGATAGGAATTATT T C CSTF3 Ensembl:ENSG00000176102 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs776030003 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6069304 RMVar_hsa_circ_99096,RMVar_hsa_circ_148913,RMVar_hsa_circ_148915 46294 RMVar_ID_46294 Human_SNP_ID_461469963 A-to-I Human chr11 - 33161034 33161034 33161034 GGCTGCTTCGTCCTATTTAGATTCATGGGACTACTCCAGATGGGATGCTTTCCTTTGATATCGTT GGCTGCTTCGTCCTATTTAGATTCATGGGACTGCTCCAGATGGGATGCTTTCCTTTGATATCGTT T C CSTF3 Ensembl:ENSG00000176102 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1450911690 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6069304,Human_RBP_ID_11602748 RMVar_hsa_circ_99096,RMVar_hsa_circ_148913,RMVar_hsa_circ_148915 46295 RMVar_ID_46295 Human_SNP_ID_461469967 A-to-I Human chr11 - 33161048 33161048 33161048 AGACAATAGCGGTAGGCTGCTTCGTCCTATTTAGATTCATGGGACTACTCCAGATGGGATGCTTT AGACAATAGCGGTAGGCTGCTTCGTCCTATTTTGATTCATGGGACTACTCCAGATGGGATGCTTT T A CSTF3 Ensembl:ENSG00000176102 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs923461241 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6069304 RMVar_hsa_circ_99096,RMVar_hsa_circ_148913,RMVar_hsa_circ_148915 46296 RMVar_ID_46296 Human_SNP_ID_461469974 A-to-I Human chr11 - 33161073 33161073 33161073 ATGAATACGAGTAAATACTTGATTTAGACAATAGCGGTAGGCTGCTTCGTCCTATTTAGATTCAT ATGAATACGAGTAAATACTTGATTTAGACAATGGCGGTAGGCTGCTTCGTCCTATTTAGATTCAT T C CSTF3 Ensembl:ENSG00000176102 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1327948256 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11602750 RMVar_hsa_circ_99096,RMVar_hsa_circ_148913,RMVar_hsa_circ_148915 46297 RMVar_ID_46297 Human_SNP_ID_461469976 A-to-I Human chr11 - 33161075 33161075 33161075 GCATGAATACGAGTAAATACTTGATTTAGACAATAGCGGTAGGCTGCTTCGTCCTATTTAGATTC GCATGAATACGAGTAAATACTTGATTTAGACAGTAGCGGTAGGCTGCTTCGTCCTATTTAGATTC T C CSTF3 Ensembl:ENSG00000176102 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910653628 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11602750 RMVar_hsa_circ_99096,RMVar_hsa_circ_148913,RMVar_hsa_circ_148915 46298 RMVar_ID_46298 Human_SNP_ID_461470015 A-to-I Human chr11 + 33161176 33161176 33161176 TAGATCTTGCTCCCCATTCCCACCACTCTTCTATATACCCTGTCCCCCGGGTTCACTAGACCCAA TAGATCTTGCTCCCCATTCCCACCACTCTTCTGTATACCCTGTCCCCCGGGTTCACTAGACCCAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1418645633 Functional Loss SNV dbSNP153 33..33 33 - - - 46299 RMVar_ID_46299 Human_SNP_ID_461470017 A-to-I Human chr11 + 33161180 33161180 33161180 TCTTGCTCCCCATTCCCACCACTCTTCTATATACCCTGTCCCCCGGGTTCACTAGACCCAATTCC TCTTGCTCCCCATTCCCACCACTCTTCTATATCCCCTGTCCCCCGGGTTCACTAGACCCAATTCC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs966739606 Functional Loss SNV dbSNP153 33..33 33 - - - 46300 RMVar_ID_46300 Human_SNP_ID_461470090 A-to-I Human chr11 + 33161376 33161376 33161376 CGTGCGCACTGACCGTCGATGGGAAGCTAGAAAAGAAAAATTAAACTAAAAACCACCCCCAAATC CGTGCGCACTGACCGTCGATGGGAAGCTAGAAGAGAAAAATTAAACTAAAAACCACCCCCAAATC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs192133921 Functional Loss SNV dbSNP153 33..33 33 - - - 46301 RMVar_ID_46301 Human_SNP_ID_461470094 A-to-I Human chr11 + 33161391 33161391 33161391 TCGATGGGAAGCTAGAAAAGAAAAATTAAACTAAAAACCACCCCCAAATCAGTAAAGTTACCCCC TCGATGGGAAGCTAGAAAAGAAAAATTAAACTGAAAACCACCCCCAAATCAGTAAAGTTACCCCC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs549893325 Functional Loss SNV dbSNP153 33..33 33 - - - 46302 RMVar_ID_46302 Human_SNP_ID_461470098 A-to-I Human chr11 + 33161412 33161411 33161413 AAAATTAAACTAAAAACCACCCCCAAATCAGTAAAGTTACCCCCTGCCCAGCTGAGCCAGACCGC AAAATTAAACTAAAAACCACCCCCAAATCAGT__AGTTACCCCCTGCCCAGCTGAGCCAGACCGC TAA T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1408775438 Functional Loss DEL dbSNP153 33..34 33 - - - 46303 RMVar_ID_46303 Human_SNP_ID_461470098 A-to-I Human chr11 + 33161413 33161411 33161413 AAATTAAACTAAAAACCACCCCCAAATCAGTAAAGTTACCCCCTGCCCAGCTGAGCCAGACCGCC AAATTAAACTAAAAACCACCCCCAAATCAGT__AGTTACCCCCTGCCCAGCTGAGCCAGACCGCC TAA T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1408775438 Functional Loss DEL dbSNP153 32..33 33 - - - 46304 RMVar_ID_46304 Human_SNP_ID_461497220 A-to-I Human chr11 + 33270021 33270021 33270021 ATTTTTTTAAGACAGTTTCGCTTTCGTTGCCCAAGCTGGAGTACAGTGGCGTGACCTTGGCTCAC ATTTTTTTAAGACAGTTTCGCTTTCGTTGCCCGAGCTGGAGTACAGTGGCGTGACCTTGGCTCAC A G HIPK3 Ensembl:ENSG00000110422 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1000732151 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78528,RMVar_hsa_circ_120780,RMVar_hsa_circ_148917,RMVar_hsa_circ_148918 46305 RMVar_ID_46305 Human_SNP_ID_461505264 A-to-I Human chr11 + 33300766 33300762 33300766 GTATTTTTTTGTTTTGTTTTTTTGAGAGTCTCACTCAGTCACCCAGACTGGAGTACAGTGACATG GTATTTTTTTGTTTTGTTTTTTTGAGAGT____CTCAGTCACCCAGACTGGAGTACAGTGACATG TCTCA T HIPK3 Ensembl:ENSG00000110422 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1480169538 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_148926,RMVar_hsa_circ_277593,RMVar_hsa_circ_120780,RMVar_hsa_circ_148918,RMVar_hsa_circ_369387,RMVar_hsa_circ_375959,RMVar_hsa_circ_106888,RMVar_hsa_circ_122026,RMVar_hsa_circ_273588,RMVar_hsa_circ_120485,RMVar_hsa_circ_93673,RMVar_hsa_circ_100607,RMVar_hsa_circ_148928,RMVar_hsa_circ_84492,RMVar_hsa_circ_148927,RMVar_hsa_circ_148922,RMVar_hsa_circ_148924,RMVar_hsa_circ_148925,RMVar_hsa_circ_148923,RMVar_hsa_circ_148920,RMVar_hsa_circ_148921,RMVar_hsa_circ_148919 46306 RMVar_ID_46306 Human_SNP_ID_461506132 A-to-I Human chr11 + 33304080 33304078 33304080 CCTCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCGTGCACCAGCACGTCCAGCTAATTTTT CCTCTGCCTCAGCCTCCCAAGTAGCTGGGAC__CAGGCGTGCACCAGCACGTCCAGCTAATTTTT CTA C HIPK3 Ensembl:ENSG00000110422 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1294030942 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_148926,RMVar_hsa_circ_277593,RMVar_hsa_circ_120780,RMVar_hsa_circ_148918,RMVar_hsa_circ_369387,RMVar_hsa_circ_375959,RMVar_hsa_circ_106888,RMVar_hsa_circ_122026,RMVar_hsa_circ_273588,RMVar_hsa_circ_120485,RMVar_hsa_circ_93673,RMVar_hsa_circ_100607,RMVar_hsa_circ_148928,RMVar_hsa_circ_84492,RMVar_hsa_circ_148927,RMVar_hsa_circ_148922,RMVar_hsa_circ_148924,RMVar_hsa_circ_148925,RMVar_hsa_circ_148923,RMVar_hsa_circ_148920,RMVar_hsa_circ_148921,RMVar_hsa_circ_148919 46307 RMVar_ID_46307 Human_SNP_ID_461506227 A-to-I Human chr11 + 33304374 33304374 33304374 GAATTCGGGACTTCGAGACCAACCTGACGAACATGGAGAAACCCCGTCTCTACTAAAAATACAAA GAATTCGGGACTTCGAGACCAACCTGACGAACGTGGAGAAACCCCGTCTCTACTAAAAATACAAA A G HIPK3 Ensembl:ENSG00000110422 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs995727332 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_148926,RMVar_hsa_circ_277593,RMVar_hsa_circ_120780,RMVar_hsa_circ_148918,RMVar_hsa_circ_369387,RMVar_hsa_circ_375959,RMVar_hsa_circ_106888,RMVar_hsa_circ_122026,RMVar_hsa_circ_273588,RMVar_hsa_circ_120485,RMVar_hsa_circ_93673,RMVar_hsa_circ_100607,RMVar_hsa_circ_148928,RMVar_hsa_circ_84492,RMVar_hsa_circ_148927,RMVar_hsa_circ_148922,RMVar_hsa_circ_148924,RMVar_hsa_circ_148925,RMVar_hsa_circ_148923,RMVar_hsa_circ_148920,RMVar_hsa_circ_148921,RMVar_hsa_circ_148919 46308 RMVar_ID_46308 Human_SNP_ID_461518827 A-to-I Human chr11 + 33353902 33353902 33353902 TACATTTGGGAAGCCATTCTGTGTACAGACTTAGAGCAACAGATGCACATATGTCAGAATTACAG TACATTTGGGAAGCCATTCTGTGTACAGACTTTGAGCAACAGATGCACATATGTCAGAATTACAG A T HIPK3 Ensembl:ENSG00000110422 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs560235851 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_395142,Human_RBP_ID_1778603,Human_RBP_ID_8769085,Human_RBP_ID_11603210,Human_RBP_ID_17233963,Human_RBP_ID_21883412 Human_miRNA_ID_1767417 46309 RMVar_ID_46309 Human_SNP_ID_461613605 A-to-I Human chr11 - 33741442 33741442 33741442 TAATTAGGCTAATCCATTTAGTGATTCCTAATATTTTGTACTCACAGAGAACTAATTGACTAAAC TAATTAGGCTAATCCATTTAGTGATTCCTAATGTTTTGTACTCACAGAGAACTAATTGACTAAAC T C FBXO3 Ensembl:ENSG00000110429 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1272198128 Functional Loss SNV dbSNP153 33..33 33 - - - 46310 RMVar_ID_46310 Human_SNP_ID_461690081 A-to-I Human chr11 + 34060049 34060049 34060049 AAACCCCGCCTCTATTAAAAATATGAAAAATTAGCTGGGCATGGTGGCATGCAGCTGTAGTTCCA AAACCCCGCCTCTATTAAAAATATGAAAAATTGGCTGGGCATGGTGGCATGCAGCTGTAGTTCCA A G CAPRIN1 Ensembl:ENSG00000135387 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432207648 Functional Loss SNV dbSNP153 33..33 33 - - - 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 46311 RMVar_ID_46311 Human_SNP_ID_461690084 A-to-I Human chr11 + 34060075 34060062 34060075 AAAATTAGCTGGGCATGGTGGCATGCAGCTGTAGTTCCAGCTACTTGGGAGGCCGAGACAGGAGA AAAATTAGCTGGGCATGGTG_____________GTTCCAGCTACTTGGGAGGCCGAGACAGGAGA GGCATGCAGCTGTA G CAPRIN1 Ensembl:ENSG00000135387 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1046185346 Functional Loss DEL dbSNP153 21..33 33 - - - Human_RBP_ID_11605379 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 46312 RMVar_ID_46312 Human_SNP_ID_461690088 A-to-I Human chr11 + 34060075 34060075 34060075 AAAATTAGCTGGGCATGGTGGCATGCAGCTGTAGTTCCAGCTACTTGGGAGGCCGAGACAGGAGA AAAATTAGCTGGGCATGGTGGCATGCAGCTGTGGTTCCAGCTACTTGGGAGGCCGAGACAGGAGA A G CAPRIN1 Ensembl:ENSG00000135387 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1000856916 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11605379 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 46313 RMVar_ID_46313 Human_SNP_ID_461690279 A-to-I Human chr11 + 34060629 34060625 34060629 CTTCTTTTTACATTGTGGACAGGAAAGATAGTAAGCAAAAGTTTCCTCAATTTTTAAAAGGACGA CTTCTTTTTACATTGTGGACAGGAAAGAT____AGCAAAAGTTTCCTCAATTTTTAAAAGGACGA TAGTA T CAPRIN1 Ensembl:ENSG00000135387 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1412550435 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_11766507 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 46314 RMVar_ID_46314 Human_SNP_ID_461690507 A-to-I Human chr11 + 34061323 34061323 34061323 CTGCCTCCCAGGTTCAAGTGATTCTCCTGCCTAAGCCTCCCAAGTAGCTGGTATTATAGGCAACC CTGCCTCCCAGGTTCAAGTGATTCTCCTGCCTGAGCCTCCCAAGTAGCTGGTATTATAGGCAACC A G CAPRIN1 Ensembl:ENSG00000135387 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1464781116 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11605429 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 46315 RMVar_ID_46315 Human_SNP_ID_461690508 A-to-I Human chr11 + 34061323 34061323 34061323 CTGCCTCCCAGGTTCAAGTGATTCTCCTGCCTAAGCCTCCCAAGTAGCTGGTATTATAGGCAACC CTGCCTCCCAGGTTCAAGTGATTCTCCTGCCTTAGCCTCCCAAGTAGCTGGTATTATAGGCAACC A T CAPRIN1 Ensembl:ENSG00000135387 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1464781116 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11605429 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 46316 RMVar_ID_46316 Human_SNP_ID_461690646 A-to-I Human chr11 + 34061882 34061882 34061882 AATCCCAGTTACCTGGGAGTCTGAGGCAGGAGAATCGCTGGAACCTGGGAGGCAGAGGCTGCATG AATCCCAGTTACCTGGGAGTCTGAGGCAGGAGGATCGCTGGAACCTGGGAGGCAGAGGCTGCATG A G CAPRIN1 Ensembl:ENSG00000135387 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs967501517 Functional Loss SNV dbSNP153 33..33 33 - - - 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 46317 RMVar_ID_46317 Human_SNP_ID_461690730 A-to-I Human chr11 + 34062073 34062071 34062074 CTCCCGCTACATGAGCATGCTTTCAACATTTGAAGAAAGCTGCCATGGATCAGCTATGGATTGTA CTCCCGCTACATGAGCATGCTTTCAACATTT___GAAAGCTGCCATGGATCAGCTATGGATTGTA TGAA T CAPRIN1 Ensembl:ENSG00000135387 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1382601090 Functional Loss DEL dbSNP153 32..34 33 - - - 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 46318 RMVar_ID_46318 Human_SNP_ID_461691155 A-to-I Human chr11 + 34063580 34063580 34063580 TTATTTCCCAGTACCACATGACTCTGACATCTACTGGGTGTGGTCACACCTCTCCCATGATTCCC TTATTTCCCAGTACCACATGACTCTGACATCTGCTGGGTGTGGTCACACCTCTCCCATGATTCCC A G CAPRIN1 Ensembl:ENSG00000135387 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6484694 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5664,GWAS_ID_5665,GWAS_ID_5666,GWAS_ID_5667,GWAS_ID_5668,GWAS_ID_5669,GWAS_ID_5670,GWAS_ID_5671,GWAS_ID_5672,GWAS_ID_5673,GWAS_ID_5674,GWAS_ID_5675,GWAS_ID_5676,GWAS_ID_5677,GWAS_ID_5678,GWAS_ID_5679,GWAS_ID_5680,GWAS_ID_5681,GWAS_ID_5682,GWAS_ID_5683,GWAS_ID_5684,GWAS_ID_5685,GWAS_ID_5686,GWAS_ID_5687,GWAS_ID_5688,GWAS_ID_5689,GWAS_ID_5690,GWAS_ID_5691,GWAS_ID_5692,GWAS_ID_5693,GWAS_ID_5694 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 46319 RMVar_ID_46319 Human_SNP_ID_461693375 A-to-I Human chr11 + 34071471 34071471 34071471 CCTGTAATCCCAGCTACTTTAGGGGCTGATGCAGTAGAATAGCTTGAACGTGGGAGGCAGAGGTT CCTGTAATCCCAGCTACTTTAGGGGCTGATGCGGTAGAATAGCTTGAACGTGGGAGGCAGAGGTT A G CAPRIN1 Ensembl:ENSG00000135387 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1435263421 Functional Loss SNV dbSNP153 33..33 33 - - - 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 46320 RMVar_ID_46320 Human_SNP_ID_461694937 A-to-I Human chr11 + 34076792 34076792 34076792 AGTCTACTCTGTTGCCCAGGTTGGAGTGTAGTAGTGTGATCTCAGCTCACAGCAACCTCCGCCTC AGTCTACTCTGTTGCCCAGGTTGGAGTGTAGTCGTGTGATCTCAGCTCACAGCAACCTCCGCCTC A C CAPRIN1 Ensembl:ENSG00000135387 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs897862219 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8350407,Human_RBP_ID_11605944 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_6176,RMVar_hsa_circ_315538,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_148994,RMVar_hsa_circ_102755,RMVar_hsa_circ_332163,RMVar_hsa_circ_353773,RMVar_hsa_circ_357235,RMVar_hsa_circ_366718,RMVar_hsa_circ_343294,RMVar_hsa_circ_54105,RMVar_hsa_circ_273531,RMVar_hsa_circ_64739,RMVar_hsa_circ_148996,RMVar_hsa_circ_18872,RMVar_hsa_circ_10494,RMVar_hsa_circ_19666,RMVar_hsa_circ_349096,RMVar_hsa_circ_352122,RMVar_hsa_circ_113513,RMVar_hsa_circ_149000,RMVar_hsa_circ_86955,RMVar_hsa_circ_336186,RMVar_hsa_circ_343747,RMVar_hsa_circ_84223,RMVar_hsa_circ_149001,RMVar_hsa_circ_149002 46321 RMVar_ID_46321 Human_SNP_ID_461695517 A-to-I Human chr11 + 34079248 34079248 34079248 ATGGTAAAACCTTGCCTCTACTGAAAATACAAAAATTGGCTGGACGTGGTGGTACACGCCTGTAA ATGGTAAAACCTTGCCTCTACTGAAAATACAAGAATTGGCTGGACGTGGTGGTACACGCCTGTAA A G CAPRIN1 Ensembl:ENSG00000135387 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935167329 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11606062,Human_RBP_ID_23305445,Human_RBP_ID_24883168 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_6176,RMVar_hsa_circ_315538,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_148994,RMVar_hsa_circ_102755,RMVar_hsa_circ_332163,RMVar_hsa_circ_353773,RMVar_hsa_circ_357235,RMVar_hsa_circ_366718,RMVar_hsa_circ_343294,RMVar_hsa_circ_54105,RMVar_hsa_circ_273531,RMVar_hsa_circ_64739,RMVar_hsa_circ_148996,RMVar_hsa_circ_18872,RMVar_hsa_circ_10494,RMVar_hsa_circ_19666,RMVar_hsa_circ_349096,RMVar_hsa_circ_352122,RMVar_hsa_circ_113513,RMVar_hsa_circ_149000,RMVar_hsa_circ_86955,RMVar_hsa_circ_336186,RMVar_hsa_circ_343747,RMVar_hsa_circ_84223,RMVar_hsa_circ_149001,RMVar_hsa_circ_149002 46322 RMVar_ID_46322 Human_SNP_ID_461695527 A-to-I Human chr11 + 34079279 34079279 34079279 AAAATTGGCTGGACGTGGTGGTACACGCCTGTAATCTCAGCTACTTGGGTGGCTGAGGAACAAGA AAAATTGGCTGGACGTGGTGGTACACGCCTGTGATCTCAGCTACTTGGGTGGCTGAGGAACAAGA A G CAPRIN1 Ensembl:ENSG00000135387 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006866345 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22790271 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_6176,RMVar_hsa_circ_315538,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_148994,RMVar_hsa_circ_102755,RMVar_hsa_circ_332163,RMVar_hsa_circ_353773,RMVar_hsa_circ_357235,RMVar_hsa_circ_366718,RMVar_hsa_circ_343294,RMVar_hsa_circ_54105,RMVar_hsa_circ_273531,RMVar_hsa_circ_64739,RMVar_hsa_circ_148996,RMVar_hsa_circ_18872,RMVar_hsa_circ_10494,RMVar_hsa_circ_19666,RMVar_hsa_circ_349096,RMVar_hsa_circ_352122,RMVar_hsa_circ_113513,RMVar_hsa_circ_149000,RMVar_hsa_circ_86955,RMVar_hsa_circ_336186,RMVar_hsa_circ_343747,RMVar_hsa_circ_84223,RMVar_hsa_circ_149001,RMVar_hsa_circ_149002 46323 RMVar_ID_46323 Human_SNP_ID_461698195 A-to-I Human chr11 + 34088035 34088035 34088035 TATTTGTTTATTTAGAGACGCAGTCTCGCTCTATCGCCAGGCTGGAGTGCAGTGGCGCATTCTTG TATTTGTTTATTTAGAGACGCAGTCTCGCTCTGTCGCCAGGCTGGAGTGCAGTGGCGCATTCTTG A G CAPRIN1 Ensembl:ENSG00000135387 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs758023034 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1867,RMVar_hsa_circ_91371,RMVar_hsa_circ_100857,RMVar_hsa_circ_126497,RMVar_hsa_circ_148986,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_148994,RMVar_hsa_circ_102755,RMVar_hsa_circ_353773,RMVar_hsa_circ_357235,RMVar_hsa_circ_366718,RMVar_hsa_circ_343294,RMVar_hsa_circ_149008,RMVar_hsa_circ_19666,RMVar_hsa_circ_86955,RMVar_hsa_circ_84223,RMVar_hsa_circ_271765,RMVar_hsa_circ_149001,RMVar_hsa_circ_149002,RMVar_hsa_circ_316383,RMVar_hsa_circ_306085,RMVar_hsa_circ_274498,RMVar_hsa_circ_74569,RMVar_hsa_circ_149009,RMVar_hsa_circ_149007,RMVar_hsa_circ_41926,RMVar_hsa_circ_281248,RMVar_hsa_circ_87599,RMVar_hsa_circ_149010,RMVar_hsa_circ_84718,RMVar_hsa_circ_33542,RMVar_hsa_circ_95791,RMVar_hsa_circ_298047,RMVar_hsa_circ_149013,RMVar_hsa_circ_149014,RMVar_hsa_circ_373330,RMVar_hsa_circ_106228,RMVar_hsa_circ_295814,RMVar_hsa_circ_149018,RMVar_hsa_circ_149020,RMVar_hsa_circ_149022,RMVar_hsa_circ_82654,RMVar_hsa_circ_149021,RMVar_hsa_circ_149019,RMVar_hsa_circ_346373,RMVar_hsa_circ_149017,RMVar_hsa_circ_362806,RMVar_hsa_circ_305542,RMVar_hsa_circ_335867,RMVar_hsa_circ_149023,RMVar_hsa_circ_149025 46324 RMVar_ID_46324 Human_SNP_ID_461698246 A-to-I Human chr11 + 34088184 34088184 34088184 ACCACACTACACCCAGCTAATTTTTGTATTTTAAGTAGAGATGGGGTTTCACCATGTTGGCCAGG ACCACACTACACCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGG A T CAPRIN1 Ensembl:ENSG00000135387 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1002728287 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1867,RMVar_hsa_circ_91371,RMVar_hsa_circ_100857,RMVar_hsa_circ_126497,RMVar_hsa_circ_148986,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_148994,RMVar_hsa_circ_102755,RMVar_hsa_circ_353773,RMVar_hsa_circ_357235,RMVar_hsa_circ_366718,RMVar_hsa_circ_343294,RMVar_hsa_circ_149008,RMVar_hsa_circ_19666,RMVar_hsa_circ_86955,RMVar_hsa_circ_84223,RMVar_hsa_circ_271765,RMVar_hsa_circ_149001,RMVar_hsa_circ_149002,RMVar_hsa_circ_316383,RMVar_hsa_circ_306085,RMVar_hsa_circ_274498,RMVar_hsa_circ_74569,RMVar_hsa_circ_149009,RMVar_hsa_circ_149007,RMVar_hsa_circ_41926,RMVar_hsa_circ_281248,RMVar_hsa_circ_87599,RMVar_hsa_circ_149010,RMVar_hsa_circ_84718,RMVar_hsa_circ_33542,RMVar_hsa_circ_95791,RMVar_hsa_circ_298047,RMVar_hsa_circ_149013,RMVar_hsa_circ_149014,RMVar_hsa_circ_373330,RMVar_hsa_circ_106228,RMVar_hsa_circ_295814,RMVar_hsa_circ_149018,RMVar_hsa_circ_149020,RMVar_hsa_circ_149022,RMVar_hsa_circ_82654,RMVar_hsa_circ_149021,RMVar_hsa_circ_149019,RMVar_hsa_circ_346373,RMVar_hsa_circ_149017,RMVar_hsa_circ_362806,RMVar_hsa_circ_305542,RMVar_hsa_circ_335867,RMVar_hsa_circ_149023,RMVar_hsa_circ_149025 46325 RMVar_ID_46325 Human_SNP_ID_461698314 A-to-I Human chr11 + 34088392 34088392 34088392 GTTATGTTAACATATATTGAGCCGGGTATGGTAGCTCATGCCTGTAATCTCAGTGCTTTGGGAGG GTTATGTTAACATATATTGAGCCGGGTATGGTGGCTCATGCCTGTAATCTCAGTGCTTTGGGAGG A G CAPRIN1 Ensembl:ENSG00000135387 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1565095560 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17559895 RMVar_hsa_circ_1867,RMVar_hsa_circ_91371,RMVar_hsa_circ_100857,RMVar_hsa_circ_126497,RMVar_hsa_circ_148986,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_148994,RMVar_hsa_circ_102755,RMVar_hsa_circ_353773,RMVar_hsa_circ_357235,RMVar_hsa_circ_366718,RMVar_hsa_circ_343294,RMVar_hsa_circ_149008,RMVar_hsa_circ_19666,RMVar_hsa_circ_86955,RMVar_hsa_circ_84223,RMVar_hsa_circ_271765,RMVar_hsa_circ_149001,RMVar_hsa_circ_149002,RMVar_hsa_circ_316383,RMVar_hsa_circ_306085,RMVar_hsa_circ_274498,RMVar_hsa_circ_74569,RMVar_hsa_circ_149009,RMVar_hsa_circ_149007,RMVar_hsa_circ_41926,RMVar_hsa_circ_281248,RMVar_hsa_circ_87599,RMVar_hsa_circ_149010,RMVar_hsa_circ_84718,RMVar_hsa_circ_33542,RMVar_hsa_circ_95791,RMVar_hsa_circ_298047,RMVar_hsa_circ_149013,RMVar_hsa_circ_149014,RMVar_hsa_circ_373330,RMVar_hsa_circ_106228,RMVar_hsa_circ_295814,RMVar_hsa_circ_149018,RMVar_hsa_circ_149020,RMVar_hsa_circ_149022,RMVar_hsa_circ_82654,RMVar_hsa_circ_149021,RMVar_hsa_circ_149019,RMVar_hsa_circ_346373,RMVar_hsa_circ_149017,RMVar_hsa_circ_362806,RMVar_hsa_circ_305542,RMVar_hsa_circ_335867,RMVar_hsa_circ_149023,RMVar_hsa_circ_149025 46326 RMVar_ID_46326 Human_SNP_ID_461698493 A-to-I Human chr11 + 34089011 34089011 34089011 CCTTTAATTGCTGGGCATGGTGGTTCATTCCTATAATCCCAGCACTTTGGGAGGCTGAGGTGGGC CCTTTAATTGCTGGGCATGGTGGTTCATTCCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGC A G CAPRIN1 Ensembl:ENSG00000135387 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs538469126 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1867,RMVar_hsa_circ_91371,RMVar_hsa_circ_100857,RMVar_hsa_circ_126497,RMVar_hsa_circ_148986,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_148994,RMVar_hsa_circ_102755,RMVar_hsa_circ_353773,RMVar_hsa_circ_357235,RMVar_hsa_circ_366718,RMVar_hsa_circ_343294,RMVar_hsa_circ_149008,RMVar_hsa_circ_19666,RMVar_hsa_circ_86955,RMVar_hsa_circ_84223,RMVar_hsa_circ_271765,RMVar_hsa_circ_149001,RMVar_hsa_circ_149002,RMVar_hsa_circ_316383,RMVar_hsa_circ_306085,RMVar_hsa_circ_274498,RMVar_hsa_circ_74569,RMVar_hsa_circ_149009,RMVar_hsa_circ_149007,RMVar_hsa_circ_41926,RMVar_hsa_circ_281248,RMVar_hsa_circ_87599,RMVar_hsa_circ_149010,RMVar_hsa_circ_84718,RMVar_hsa_circ_33542,RMVar_hsa_circ_95791,RMVar_hsa_circ_298047,RMVar_hsa_circ_149013,RMVar_hsa_circ_149014,RMVar_hsa_circ_373330,RMVar_hsa_circ_106228,RMVar_hsa_circ_295814,RMVar_hsa_circ_149018,RMVar_hsa_circ_149020,RMVar_hsa_circ_149022,RMVar_hsa_circ_82654,RMVar_hsa_circ_149021,RMVar_hsa_circ_149019,RMVar_hsa_circ_346373,RMVar_hsa_circ_149017,RMVar_hsa_circ_362806,RMVar_hsa_circ_305542,RMVar_hsa_circ_335867,RMVar_hsa_circ_149023,RMVar_hsa_circ_149025 46327 RMVar_ID_46327 Human_SNP_ID_461723000 A-to-I Human chr11 - 34177770 34177770 34177770 TGAGCTTAGGAGTCGAGACCAGCCTGGGCAACATGGTGAAACCCCATCTCTGCTAAAAATATAAA TGAGCTTAGGAGTCGAGACCAGCCTGGGCAACTTGGTGAAACCCCATCTCTGCTAAAAATATAAA T A ABTB2 Ensembl:ENSG00000166016 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1337020901 Functional Loss SNV dbSNP153 33..33 33 - - - 46328 RMVar_ID_46328 Human_SNP_ID_461750562 A-to-I Human chr11 - 34294177 34294177 34294177 TATGGCCCTCCACCACTCCTGGCTAACTTTTTAAATTTTTTGTAGAGATGAGGTTTTGCCATATT TATGGCCCTCCACCACTCCTGGCTAACTTTTTTAATTTTTTGTAGAGATGAGGTTTTGCCATATT T A ABTB2 Ensembl:ENSG00000166016 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1386761994 Functional Loss SNV dbSNP153 33..33 33 - - - 46329 RMVar_ID_46329 Human_SNP_ID_461756155 A-to-I Human chr11 - 34317667 34317667 34317667 ACCTCCGCCTCCCAGGCTCAAGTGATCCTCCCACCTCATCCTCTCAAGTAGCTGGGACTACAGGC ACCTCCGCCTCCCAGGCTCAAGTGATCCTCCCTCCTCATCCTCTCAAGTAGCTGGGACTACAGGC T A ABTB2 Ensembl:ENSG00000166016 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569986842 Functional Loss SNV dbSNP153 33..33 33 - - - 46330 RMVar_ID_46330 Human_SNP_ID_461757836 A-to-I Human chr11 - 34325096 34325096 34325096 TTTGAATCTGAAGTTAAAACTGGGAAGTGTCCAGGTATGGTGGCTCATACCTGTAATCCCAGCAC TTTGAATCTGAAGTTAAAACTGGGAAGTGTCCTGGTATGGTGGCTCATACCTGTAATCCCAGCAC T A ABTB2 Ensembl:ENSG00000166016 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1387194977 Functional Loss SNV dbSNP153 33..33 33 - - - 46331 RMVar_ID_46331 Human_SNP_ID_461758212 A-to-I Human chr11 - 34326589 34326589 34326589 GTCTCCCTCTGACACCCAGGCTGGAATGCAGTAGCATGATCTCGGCTCACTGCAACCTCTGCCTC GTCTCCCTCTGACACCCAGGCTGGAATGCAGTGGCATGATCTCGGCTCACTGCAACCTCTGCCTC T C ABTB2 Ensembl:ENSG00000166016 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1564933128 Functional Loss SNV dbSNP153 33..33 33 - - - 46332 RMVar_ID_46332 Human_SNP_ID_461758316 A-to-I Human chr11 - 34327012 34327012 34327012 ATAGTGTAGTGGCGCAATCTTGGCTCACTGCAACCTCCACCTCCCGGGTTTAAGCGATTCTCCTG ATAGTGTAGTGGCGCAATCTTGGCTCACTGCAGCCTCCACCTCCCGGGTTTAAGCGATTCTCCTG T C ABTB2 Ensembl:ENSG00000166016 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1564933232 Functional Loss SNV dbSNP153 33..33 33 - - - 46333 RMVar_ID_46333 Human_SNP_ID_461915378 A-to-I Human chr11 + 34968138 34968138 34968138 ACAAAAAAATTTTAAAATCAGCTGGATGTGGTAGTGTGTGCCTGTAGTCCAACTACTCAGGCGGT ACAAAAAAATTTTAAAATCAGCTGGATGTGGTCGTGTGTGCCTGTAGTCCAACTACTCAGGCGGT A C PDHX Ensembl:ENSG00000110435 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs563803693 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_46641,RMVar_hsa_circ_149097,RMVar_hsa_circ_293194,RMVar_hsa_circ_308750,RMVar_hsa_circ_351659,RMVar_hsa_circ_368092,RMVar_hsa_circ_149099,RMVar_hsa_circ_149098,RMVar_hsa_circ_342942,RMVar_hsa_circ_306454,RMVar_hsa_circ_305246,RMVar_hsa_circ_291524,RMVar_hsa_circ_149100,RMVar_hsa_circ_149102,RMVar_hsa_circ_149103,RMVar_hsa_circ_149101,RMVar_hsa_circ_303558,RMVar_hsa_circ_272750,RMVar_hsa_circ_273925,RMVar_hsa_circ_149104,RMVar_hsa_circ_149106,RMVar_hsa_circ_149107,RMVar_hsa_circ_149105,RMVar_hsa_circ_297217,RMVar_hsa_circ_363424,RMVar_hsa_circ_42245,RMVar_hsa_circ_60807,RMVar_hsa_circ_351612,RMVar_hsa_circ_308560,RMVar_hsa_circ_149110 46334 RMVar_ID_46334 Human_SNP_ID_461987944 A-to-I Human chr11 - 35263382 35263382 35263382 CTCACCACAACCTCCGCCTCCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCTCGAGTAGCTGGG CTCACCACAACCTCCGCCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCTCGAGTAGCTGGG T C SLC1A2 Ensembl:ENSG00000110436 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1052577149 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267698 46335 RMVar_ID_46335 Human_SNP_ID_462010163 A-to-I Human chr11 - 35357052 35357052 35357052 TAGTTTTAACAGAGACGGGGTTTTACCATGTTAGATAGGATGGTCTCGATCTCCTGACCTCATGA TAGTTTTAACAGAGACGGGGTTTTACCATGTTGGATAGGATGGTCTCGATCTCCTGACCTCATGA T C SLC1A2 Ensembl:ENSG00000110436 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1171564616 Functional Loss SNV dbSNP153 33..33 33 - - - 46336 RMVar_ID_46336 Human_SNP_ID_462089476 A-to-I Human chr11 + 35691738 35691738 35691738 ATGATCTCGAGTTACTGTAAGCTCCACCTCCCAGGTTCACACCATTCTCCTGCCTCAGCCTCCCA ATGATCTCGAGTTACTGTAAGCTCCACCTCCCGGGTTCACACCATTCTCCTGCCTCAGCCTCCCA A G TRIM44 Ensembl:ENSG00000166326 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1244827842 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_149165,RMVar_hsa_circ_127668,RMVar_hsa_circ_268949,RMVar_hsa_circ_149164,RMVar_hsa_circ_378092 46337 RMVar_ID_46337 Human_SNP_ID_462163205 A-to-I Human chr11 - 35997372 35997372 35997372 GGAAAGAAACAGAAAAACATTAAACACAATGGAAATATCACTTTTGATGAGATTGTCAACATTGC GGAAAGAAACAGAAAAACATTAAACACAATGGGAATATCACTTTTGATGAGATTGTCAACATTGC T C RPL12P31 Ensembl:ENSG00000241228 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1274786447 Functional Loss SNV dbSNP153 33..33 33 - - - 46338 RMVar_ID_46338 Human_SNP_ID_462195702 A-to-I Human chr11 + 36133811 36133811 36133811 CGCCTGCCTCAGCCTCCCAAAGTGTTGGTATTACAGGCATGAGCCACCGCGCCCGGCCCATTTTC CGCCTGCCTCAGCCTCCCAAAGTGTTGGTATTGCAGGCATGAGCCACCGCGCCCGGCCCATTTTC A G LDLRAD3 Ensembl:ENSG00000179241 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs192466748 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111093,RMVar_hsa_circ_149169,RMVar_hsa_circ_149172,RMVar_hsa_circ_94278,RMVar_hsa_circ_149173 46339 RMVar_ID_46339 Human_SNP_ID_462200072 A-to-I Human chr11 + 36150256 36150256 36150256 CTCTTTAAAGATTCCCTGTTGAAGGCAGGCACAGTGGCTCACACGTGTAATCTCAACACTTTGGG CTCTTTAAAGATTCCCTGTTGAAGGCAGGCACCGTGGCTCACACGTGTAATCTCAACACTTTGGG A C LDLRAD3 Ensembl:ENSG00000179241 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1475522368 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111093,RMVar_hsa_circ_149169,RMVar_hsa_circ_149172,RMVar_hsa_circ_94278,RMVar_hsa_circ_149173 46340 RMVar_ID_46340 Human_SNP_ID_462276531 A-to-I Human chr11 - 36471595 36471595 36471595 TTACTTCATAAAATTGCTCAGAGGACTACACAAAACAAAAGAATATGAAATACTTAGGATGGTGC TTACTTCATAAAATTGCTCAGAGGACTACACAGAACAAAAGAATATGAAATACTTAGGATGGTGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1433894925 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11612391 46341 RMVar_ID_46341 Human_SNP_ID_462277493 A-to-I Human chr11 + 36475384 36475384 36475384 GTCTACACAAAAACTTGCATGACAGTATTCATAGTAGCATTATGTATGATAGCCAAAACTGTAAA GTCTACACAAAAACTTGCATGACAGTATTCATCGTAGCATTATGTATGATAGCCAAAACTGTAAA A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1180232272 Functional Loss SNV dbSNP153 33..33 33 - - - 46342 RMVar_ID_46342 Human_SNP_ID_462277499 A-to-I Human chr11 + 36475414 36475413 36475414 ATAGTAGCATTATGTATGATAGCCAAAACTGTAAACAATCTAAATGCCCATCAGTTGAGACATGC ATAGTAGCATTATGTATGATAGCCAAAACTGT_AACAATCTAAATGCCCATCAGTTGAGACATGC TA T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1283193705 Functional Loss DEL dbSNP153 33..33 33 - - - 46343 RMVar_ID_46343 Human_SNP_ID_462280278 A-to-I Human chr11 - 36487008 36487008 36487008 CGGCTCACTGCAACCTCCACCTCCCGGGCTCAAGCCATTCTCCTGCCTCAGCCTCCCAAGCAGCT CGGCTCACTGCAACCTCCACCTCCCGGGCTCAGGCCATTCTCCTGCCTCAGCCTCCCAAGCAGCT T C TRAF6 Ensembl:ENSG00000175104 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1382146456 Functional Loss SNV dbSNP153 33..33 33 - - - 46344 RMVar_ID_46344 Human_SNP_ID_462682255 A-to-I Human chr11 - 38077548 38077548 38077548 TCACTTTGCTGTACAATAGATCTCTCAAATTTATTCCTCCAATCTAACTGTAATTATATATCCTT TCACTTTGCTGTACAATAGATCTCTCAAATTTTTTCCTCCAATCTAACTGTAATTATATATCCTT T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1208274220 Functional Loss SNV dbSNP153 33..33 33 - - - 46345 RMVar_ID_46345 Human_SNP_ID_370057278 A-to-I Human chr8 - 79664946 79664946 79664946 TTTTTAAACCATGTCATACATTCCCCATCCTGATATCGCATGATCCATTATAATATAGGCAGGGG TTTTTAAACCATGTCATACATTCCCCATCCTGTTATCGCATGATCCATTATAATATAGGCAGGGG T A - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1356532017 Functional Loss SNV dbSNP153 33..33 33 - - - 46346 RMVar_ID_46346 Human_SNP_ID_370115253 A-to-I Human chr8 - 79919090 79919090 79919090 GGTTGCGGCTATTAGATCTTGAACTTACGTCTAGGTTCCTGGGAGCAACAACAGATACAACTGTA GGTTGCGGCTATTAGATCTTGAACTTACGTCTGGGTTCCTGGGAGCAACAACAGATACAACTGTA T C AC036214.3,MRPS28 Ensembl:ENSG00000276418,Ensembl:ENSG00000147586 Protein coding,Protein coding 3'UTR,CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs747839229 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1699201,Human_RBP_ID_9405569,Human_RBP_ID_16477711,Human_RBP_ID_22775715,Human_RBP_ID_26189481,Human_RBP_ID_27570035,Human_RBP_ID_27831964 Human_Splice_Rec_987760,Human_Splice_Rec_987764,Human_Splice_Rec_987770,Human_Splice_Rec_987772,Human_Splice_Rec_987776,Human_Splice_Rec_987782,Human_Splice_Rec_987788,Human_Splice_Rec_987806 RMVar_hsa_circ_252812,RMVar_hsa_circ_252813,RMVar_hsa_circ_252814 46347 RMVar_ID_46347 Human_SNP_ID_370143411 A-to-I Human chr8 - 80036833 80036833 80036833 TTTGTTATTTATTAAATTGTGATTGTTTTATTATTGTTTATGCCAAATGTTAACTGCCAAGCTTG TTTGTTATTTATTAAATTGTGATTGTTTTATTTTTGTTTATGCCAAATGTTAACTGCCAAGCTTG T A AC036214.3,TPD52 Ensembl:ENSG00000276418,Ensembl:ENSG00000076554 Protein coding,Protein coding intron,3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs914205028 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1699227,Human_RBP_ID_2057570,Human_RBP_ID_3171956,Human_RBP_ID_3882864,Human_RBP_ID_7859157,Human_RBP_ID_8952043,Human_RBP_ID_16479374,Human_RBP_ID_18392582,Human_RBP_ID_24269040,Human_RBP_ID_24521103,Human_RBP_ID_26557341,Human_RBP_ID_26734223 Human_miRNA_ID_1089479 RMVar_hsa_circ_58911,RMVar_hsa_circ_57255 46348 RMVar_ID_46348 Human_SNP_ID_370152725 A-to-I Human chr8 - 80076865 80076865 80076865 CTCATGAGTTTGTGACCAGCCATCATGGTGAAACCCCATCTCTACCAAAAGTAAAAGAATTAATC CTCATGAGTTTGTGACCAGCCATCATGGTGAAGCCCCATCTCTACCAAAAGTAAAAGAATTAATC T C AC036214.3,TPD52 Ensembl:ENSG00000276418,Ensembl:ENSG00000076554 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1344863511 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55323,RMVar_hsa_circ_69300,RMVar_hsa_circ_252817 46349 RMVar_ID_46349 Human_SNP_ID_370154947 A-to-I Human chr8 - 80086180 80086180 80086180 CGGGGAGGCGGAGGTTGTGGTGAGTCAAGATCACGACACTGCACTCCAGCCTGGCAACAGAGTGA CGGGGAGGCGGAGGTTGTGGTGAGTCAAGATCCCGACACTGCACTCCAGCCTGGCAACAGAGTGA T G TPD52 Ensembl:ENSG00000076554 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1284926734 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16479710,Human_RBP_ID_26183033 RMVar_hsa_circ_55323,RMVar_hsa_circ_69300 46350 RMVar_ID_46350 Human_SNP_ID_370159740 A-to-I Human chr8 - 80105872 80105872 80105872 CAAAAGTTAGCTGGGCGTGGTGGTGAGCACCTATAATCCCAGCTACTTGGGAGGCTGAAGCTGGG CAAAAGTTAGCTGGGCGTGGTGGTGAGCACCTGTAATCCCAGCTACTTGGGAGGCTGAAGCTGGG T C TPD52 Ensembl:ENSG00000076554 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1185146241 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55323,RMVar_hsa_circ_69300 46351 RMVar_ID_46351 Human_SNP_ID_370174308 A-to-I Human chr8 - 80166435 80166435 80166435 CTGAGGTCGGGAGTTGGAGACCCGCCTGACCAACATGGAGAAACCCTGTCTCTACTAAAAATACA CTGAGGTCGGGAGTTGGAGACCCGCCTGACCAGCATGGAGAAACCCTGTCTCTACTAAAAATACA T C TPD52 Ensembl:ENSG00000076554 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017097431 Functional Loss SNV dbSNP153 33..33 33 - - - 46352 RMVar_ID_46352 Human_SNP_ID_370174309 A-to-I Human chr8 - 80166435 80166435 80166435 CTGAGGTCGGGAGTTGGAGACCCGCCTGACCAACATGGAGAAACCCTGTCTCTACTAAAAATACA CTGAGGTCGGGAGTTGGAGACCCGCCTGACCACCATGGAGAAACCCTGTCTCTACTAAAAATACA T G TPD52 Ensembl:ENSG00000076554 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017097431 Functional Loss SNV dbSNP153 33..33 33 - - - 46353 RMVar_ID_46353 Human_SNP_ID_370174959 A-to-I Human chr8 - 80169227 80169227 80169227 CCTGTAATCCCAGCACTTTGGGAAGCTGAGGCAGGCAGATCACTTGAGGCCAGGAGTTTGACCCC CCTGTAATCCCAGCACTTTGGGAAGCTGAGGCTGGCAGATCACTTGAGGCCAGGAGTTTGACCCC T A TPD52 Ensembl:ENSG00000076554 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1395896349 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26183190 46354 RMVar_ID_46354 Human_SNP_ID_370528202 A-to-I Human chr8 - 81653105 81653105 81653105 TGCCCAGGCTGAATCTCAAATTCCTGGGCTCAAGGATCCTCCCCCCTTGGCCTCTCAAGTGCTGG TGCCCAGGCTGAATCTCAAATTCCTGGGCTCAGGGATCCTCCCCCCTTGGCCTCTCAAGTGCTGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs536053310 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_252854 46355 RMVar_ID_46355 Human_SNP_ID_370529279 A-to-I Human chr8 - 81657369 81657364 81657369 CTATGTTGCTTAGGCTGGTCTCATTGGGCTCAAGTGATCCTCCTGCCTCAGCCTTCTAAAGTGCT CTATGTTGCTTAGGCTGGTCTCATTGGGCTCA_____TCCTCCTGCCTCAGCCTTCTAAAGTGCT ATCACT A IMPA1 Ensembl:ENSG00000133731 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1211344043 Functional Loss DEL dbSNP153 33..37 33 - - - Human_RBP_ID_16482217 RMVar_hsa_circ_116905,RMVar_hsa_circ_252854,RMVar_hsa_circ_252855 46356 RMVar_ID_46356 Human_SNP_ID_370529443 A-to-I Human chr8 - 81658167 81658167 81658167 GTAGGTTCGTTTGAGCTTTGTGTTGTAAAATTAAAAATGCTTCTGTAAAGTTTTCAAGGTAGGGA GTAGGTTCGTTTGAGCTTTGTGTTGTAAAATTTAAAATGCTTCTGTAAAGTTTTCAAGGTAGGGA T A IMPA1 Ensembl:ENSG00000133731 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs949562431 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_704763,Human_RBP_ID_8952047,Human_RBP_ID_18185268,Human_RBP_ID_18392869,Human_RBP_ID_24269583 RMVar_hsa_circ_116905,RMVar_hsa_circ_252854,RMVar_hsa_circ_252855 46357 RMVar_ID_46357 Human_SNP_ID_370533923 A-to-I Human chr8 - 81676912 81676912 81676912 ATGGCTCACTGCAGCCTTGACCTTCTGGGCTCAAGGGATCCTTCTGCCTCAGCCTACCGGGGAAG ATGGCTCACTGCAGCCTTGACCTTCTGGGCTCGAGGGATCCTTCTGCCTCAGCCTACCGGGGAAG T C IMPA1 Ensembl:ENSG00000133731 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1485826113 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_42485,RMVar_hsa_circ_252854,RMVar_hsa_circ_303565,RMVar_hsa_circ_56531,RMVar_hsa_circ_55750,RMVar_hsa_circ_357113 46358 RMVar_ID_46358 Human_SNP_ID_370540071 A-to-I Human chr8 - 81697578 81697578 81697578 ACTAAAAATACAAAAATTTGCTGGGCATGATGACAAACACCTGTAATCCCTGCTACTCACAAGGC ACTAAAAATACAAAAATTTGCTGGGCATGATGGCAAACACCTGTAATCCCTGCTACTCACAAGGC T C lnc-SLC10A5-1 RNACentral:URS00008BFD6D lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs6415648 Functional Loss SNV dbSNP153 33..33 33 - - - 46359 RMVar_ID_46359 Human_SNP_ID_370540848 A-to-I Human chr8 - 81700723 81700723 81700723 GTTGGTCAGGCTGGTCTGAAACTCCCGACCTCAGGTGATCTGCCTACCTCAGCCTCACAAAGTGC GTTGGTCAGGCTGGTCTGAAACTCCCGACCTCGGGTGATCTGCCTACCTCAGCCTCACAAAGTGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1262041523 Functional Loss SNV dbSNP153 33..33 33 - - - 46360 RMVar_ID_46360 Human_SNP_ID_370541241 A-to-I Human chr8 - 81702437 81702437 81702437 TTCATTAGTTTATGCTGTAGTGACAACAACAAAGATGTATTTCCTGGTGGGGGATGTCAGCTGTT TTCATTAGTTTATGCTGTAGTGACAACAACAAGGATGTATTTCCTGGTGGGGGATGTCAGCTGTT T C ZFAND1 Ensembl:ENSG00000104231 Protein coding exon GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1036362518 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_704833,Human_RBP_ID_7860735,Human_RBP_ID_9228416,Human_RBP_ID_16482802,Human_RBP_ID_18392889,Human_RBP_ID_22410467,Human_RBP_ID_22837261,Human_RBP_ID_27779771 46361 RMVar_ID_46361 Human_SNP_ID_370541747 A-to-I Human chr8 - 81704286 81704286 81704286 ACAATTTGCCTGCCTTAACCTCCCGAAGTGCTAGGATTATAGGCATGAGCCATCATGCTCAGCCA ACAATTTGCCTGCCTTAACCTCCCGAAGTGCTGGGATTATAGGCATGAGCCATCATGCTCAGCCA T C ZFAND1 Ensembl:ENSG00000104231 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1295788166 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_956,RMVar_hsa_circ_28826 46362 RMVar_ID_46362 Human_SNP_ID_371180026 A-to-I Human chr8 + 84195329 84195329 84195329 GGGTGTGGTGGCATGCGCCTGTAGTCCCAGCTACTCAGGAGGCTAAGGAAGGAGAATTGTTTGAA GGGTGTGGTGGCATGCGCCTGTAGTCCCAGCTGCTCAGGAGGCTAAGGAAGGAGAATTGTTTGAA A G RALYL Ensembl:ENSG00000184672 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1195315400 Functional Loss SNV dbSNP153 33..33 33 - - - 46363 RMVar_ID_46363 Human_SNP_ID_371188250 A-to-I Human chr8 + 84228670 84228670 84228670 CACACTCTGTATTGGTCTGGTCTCATAATGCTATGAAGAAATACCTGAGTCTGGGTAATTCATAA CACACTCTGTATTGGTCTGGTCTCATAATGCTGTGAAGAAATACCTGAGTCTGGGTAATTCATAA A G RALYL Ensembl:ENSG00000184672 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1482866746 Functional Loss SNV dbSNP153 33..33 33 - - - 46364 RMVar_ID_46364 Human_SNP_ID_371188260 A-to-I Human chr8 + 84228720 84228720 84228720 CTGGGTAATTCATAAAGAAAAGAGGTTTAATTAACTCACAGATCTGCATGGCTTGGGAGGCCTCA CTGGGTAATTCATAAAGAAAAGAGGTTTAATTGACTCACAGATCTGCATGGCTTGGGAGGCCTCA A G RALYL Ensembl:ENSG00000184672 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1298146777 Functional Loss SNV dbSNP153 33..33 33 - - - 46365 RMVar_ID_46365 Human_SNP_ID_371194594 A-to-I Human chr8 + 84254975 84254975 84254975 ACACGAACAGCATGGGGGAAACTGCTTCCATGATCCAATTATCTCCACCTCGTCTCTCCCTTGAC ACACGAACAGCATGGGGGAAACTGCTTCCATGTTCCAATTATCTCCACCTCGTCTCTCCCTTGAC A T RALYL Ensembl:ENSG00000184672 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs750381214 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28132 46366 RMVar_ID_46366 Human_SNP_ID_371195991 A-to-I Human chr8 + 84261300 84261300 84261300 TTTGGCTGTGTCGCCACAAAAATCTCATCTTTAATTGTAGTTCCCATAATCCCCACGTGTGGTGG TTTGGCTGTGTCGCCACAAAAATCTCATCTTTTATTGTAGTTCCCATAATCCCCACGTGTGGTGG A T RALYL Ensembl:ENSG00000184672 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs909626786 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28132 46367 RMVar_ID_46367 Human_SNP_ID_371196048 A-to-I Human chr8 + 84261510 84261508 84261510 AGGACATGTTTGCTTCCCCTTCTGCCATGATTATATGTTTCCTAAGGCCTCCCCAGCCCTGCAAA AGGACATGTTTGCTTCCCCTTCTGCCATGAT__TATGTTTCCTAAGGCCTCCCCAGCCCTGCAAA TTA T RALYL Ensembl:ENSG00000184672 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1253422823 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_28132 46368 RMVar_ID_46368 Human_SNP_ID_371196050 A-to-I Human chr8 + 84261510 84261510 84261510 AGGACATGTTTGCTTCCCCTTCTGCCATGATTATATGTTTCCTAAGGCCTCCCCAGCCCTGCAAA AGGACATGTTTGCTTCCCCTTCTGCCATGATTGTATGTTTCCTAAGGCCTCCCCAGCCCTGCAAA A G RALYL Ensembl:ENSG00000184672 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1490096067 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28132 46369 RMVar_ID_46369 Human_SNP_ID_371207709 A-to-I Human chr8 + 84310182 84310182 84310182 ATTCTGCCTCAGCCTCCCAAGTACCTGGGGTTACAGGCACATACCACTACTCCTGGCTAATTTTT ATTCTGCCTCAGCCTCCCAAGTACCTGGGGTTGCAGGCACATACCACTACTCCTGGCTAATTTTT A G RALYL Ensembl:ENSG00000184672 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1287906927 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28132 46370 RMVar_ID_46370 Human_SNP_ID_371209005 A-to-I Human chr8 + 84314619 84314619 84314619 ATTGTGGCACATGCCTATAGTCCCAGCTATTCAGGAAGCTGAGGCAGGAGGATCACCTGAGCCCT ATTGTGGCACATGCCTATAGTCCCAGCTATTCCGGAAGCTGAGGCAGGAGGATCACCTGAGCCCT A C RALYL Ensembl:ENSG00000184672 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs540751791 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28132 46371 RMVar_ID_46371 Human_SNP_ID_371231999 A-to-I Human chr8 + 84408341 84408341 84408341 GTTCTGAGGTTACTTAGAAAAAAACCTAGCATACTCTAATGAGATTTTCAGTAAATAGAAAAACT GTTCTGAGGTTACTTAGAAAAAAACCTAGCATCCTCTAATGAGATTTTCAGTAAATAGAAAAACT A C RALYL Ensembl:ENSG00000184672 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1037749522 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28132,RMVar_hsa_circ_252863,RMVar_hsa_circ_315711 46372 RMVar_ID_46372 Human_SNP_ID_371232000 A-to-I Human chr8 + 84408341 84408341 84408341 GTTCTGAGGTTACTTAGAAAAAAACCTAGCATACTCTAATGAGATTTTCAGTAAATAGAAAAACT GTTCTGAGGTTACTTAGAAAAAAACCTAGCATTCTCTAATGAGATTTTCAGTAAATAGAAAAACT A T RALYL Ensembl:ENSG00000184672 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1037749522 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28132,RMVar_hsa_circ_252863,RMVar_hsa_circ_315711 46373 RMVar_ID_46373 Human_SNP_ID_371232008 A-to-I Human chr8 + 84408383 84408383 84408383 GATTTTCAGTAAATAGAAAAACTCTGTCATATATGCCATACAAAGACAAATAAGGTTCAAAGTAA GATTTTCAGTAAATAGAAAAACTCTGTCATATGTGCCATACAAAGACAAATAAGGTTCAAAGTAA A G RALYL Ensembl:ENSG00000184672 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1051742725 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28132,RMVar_hsa_circ_252863,RMVar_hsa_circ_315711 46374 RMVar_ID_46374 Human_SNP_ID_371239324 A-to-I Human chr8 + 84432222 84432222 84432222 TATTATTCAGCCTTTAAGGAAAATCCTGTCATATGCAACAACATGGATGAATCTGGAAGCCATTA TATTATTCAGCCTTTAAGGAAAATCCTGTCATGTGCAACAACATGGATGAATCTGGAAGCCATTA A G RALYL Ensembl:ENSG00000184672 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs553025931 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28132,RMVar_hsa_circ_315711 46375 RMVar_ID_46375 Human_SNP_ID_371239890 A-to-I Human chr8 + 84434295 84434294 84434296 TAACTTACCCCTTTTATAATCCATCTCCAAACAGAGTCATATTTTGAGATATCGGGGGTTAGGAC TAACTTACCCCTTTTATAATCCATCTCCAAAC__AGTCATATTTTGAGATATCGGGGGTTAGGAC CAG C RALYL Ensembl:ENSG00000184672 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1339813897 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_28132,RMVar_hsa_circ_315711 46376 RMVar_ID_46376 Human_SNP_ID_371311869 A-to-I Human chr8 + 84712908 84712908 84712908 TCATGTGGTTTGCAAACATTTTCTTCCATTCCATGGTTGTCTCTTCACTCTGTTGATTATTTTTC TCATGTGGTTTGCAAACATTTTCTTCCATTCCTTGGTTGTCTCTTCACTCTGTTGATTATTTTTC A T RALYL Ensembl:ENSG00000184672 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1049402018 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_290183,RMVar_hsa_circ_330848,RMVar_hsa_circ_335783,RMVar_hsa_circ_297597,RMVar_hsa_circ_295401,RMVar_hsa_circ_277989,RMVar_hsa_circ_252871 46377 RMVar_ID_46377 Human_SNP_ID_371357013 A-to-I Human chr8 + 84898139 84898139 84898139 TTTAGTTTGGCTAAAGCAGTGGAACTCAGAGGATGGCCCAGAACCAGCAGCATCATATCATGTGG TTTAGTTTGGCTAAAGCAGTGGAACTCAGAGGCTGGCCCAGAACCAGCAGCATCATATCATGTGG A C RALYL Ensembl:ENSG00000184672 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs538634240 Functional Loss SNV dbSNP153 33..33 33 - - - 46378 RMVar_ID_46378 Human_SNP_ID_371362378 A-to-I Human chr8 + 84921204 84921204 84921204 AAATGTGAAAGGCATTTATGAATGGTAAGGGAAACACTATATACAAATGTATATTTGTAAAAGCT AAATGTGAAAGGCATTTATGAATGGTAAGGGAGACACTATATACAAATGTATATTTGTAAAAGCT A G RALYL Ensembl:ENSG00000184672 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs10094238 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5695,GWAS_ID_5696,GWAS_ID_5697,GWAS_ID_5698,GWAS_ID_5699,GWAS_ID_5700,GWAS_ID_5701,GWAS_ID_5702,GWAS_ID_5703,GWAS_ID_5704,GWAS_ID_5705,GWAS_ID_5706,GWAS_ID_5707,GWAS_ID_5708,GWAS_ID_5709,GWAS_ID_5710,GWAS_ID_5711,GWAS_ID_5712,GWAS_ID_5713,GWAS_ID_5714,GWAS_ID_5715,GWAS_ID_5716,GWAS_ID_5717,GWAS_ID_5718,GWAS_ID_5719,GWAS_ID_5720,GWAS_ID_5721,GWAS_ID_5722,GWAS_ID_5723,GWAS_ID_5724,GWAS_ID_5725,GWAS_ID_5726,GWAS_ID_5727,GWAS_ID_5728,GWAS_ID_5729,GWAS_ID_5730,GWAS_ID_5731,GWAS_ID_5732,GWAS_ID_5733,GWAS_ID_5734 46379 RMVar_ID_46379 Human_SNP_ID_371362379 A-to-I Human chr8 + 84921204 84921204 84921204 AAATGTGAAAGGCATTTATGAATGGTAAGGGAAACACTATATACAAATGTATATTTGTAAAAGCT AAATGTGAAAGGCATTTATGAATGGTAAGGGATACACTATATACAAATGTATATTTGTAAAAGCT A T RALYL Ensembl:ENSG00000184672 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs10094238 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5695,GWAS_ID_5696,GWAS_ID_5697,GWAS_ID_5698,GWAS_ID_5699,GWAS_ID_5700,GWAS_ID_5701,GWAS_ID_5702,GWAS_ID_5703,GWAS_ID_5704,GWAS_ID_5705,GWAS_ID_5706,GWAS_ID_5707,GWAS_ID_5708,GWAS_ID_5709,GWAS_ID_5710,GWAS_ID_5711,GWAS_ID_5712,GWAS_ID_5713,GWAS_ID_5714,GWAS_ID_5715,GWAS_ID_5716,GWAS_ID_5717,GWAS_ID_5718,GWAS_ID_5719,GWAS_ID_5720,GWAS_ID_5721,GWAS_ID_5722,GWAS_ID_5723,GWAS_ID_5724,GWAS_ID_5725,GWAS_ID_5726,GWAS_ID_5727,GWAS_ID_5728,GWAS_ID_5729,GWAS_ID_5730,GWAS_ID_5731,GWAS_ID_5732,GWAS_ID_5733,GWAS_ID_5734 46380 RMVar_ID_46380 Human_SNP_ID_371427402 A-to-I Human chr8 + 85179821 85179821 85179821 AGCTCGGACTACAGGCGCCCGCCAGCGCACCCAGCTAATTTTTTTGTAATTTTAGTAGAGACAGG AGCTCGGACTACAGGCGCCCGCCAGCGCACCCGGCTAATTTTTTTGTAATTTTAGTAGAGACAGG A G E2F5 Ensembl:ENSG00000133740 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1358550522 Functional Loss SNV dbSNP153 33..33 33 - - - 46381 RMVar_ID_46381 Human_SNP_ID_371427878 A-to-I Human chr8 + 85180939 85180939 85180939 TTATTCTGTCGCCCAGGCTGGAGTGCAGTGGTACAATCTCAGCTCATTGTAACCTCCACTTCCCG TTATTCTGTCGCCCAGGCTGGAGTGCAGTGGTGCAATCTCAGCTCATTGTAACCTCCACTTCCCG A G E2F5 Ensembl:ENSG00000133740 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1454317709 Functional Loss SNV dbSNP153 33..33 33 - - - 46382 RMVar_ID_46382 Human_SNP_ID_371435120 A-to-I Human chr8 + 85211840 85211838 85211840 TTTTTGTATTTTTTGTAAAGACGGATTTCACTATGTTGCCCAGGCTGGTCTGAACTCCTGAGCTC TTTTTGTATTTTTTGTAAAGACGGATTTCAC__TGTTGCCCAGGCTGGTCTGAACTCCTGAGCTC CTA C E2F5 Ensembl:ENSG00000133740 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1318638913 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_252889,RMVar_hsa_circ_323077,RMVar_hsa_circ_319443 46383 RMVar_ID_46383 Human_SNP_ID_371435121 A-to-I Human chr8 + 85211840 85211840 85211840 TTTTTGTATTTTTTGTAAAGACGGATTTCACTATGTTGCCCAGGCTGGTCTGAACTCCTGAGCTC TTTTTGTATTTTTTGTAAAGACGGATTTCACTGTGTTGCCCAGGCTGGTCTGAACTCCTGAGCTC A G E2F5 Ensembl:ENSG00000133740 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs986307937 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_252889,RMVar_hsa_circ_323077,RMVar_hsa_circ_319443 46384 RMVar_ID_46384 Human_SNP_ID_371435509 A-to-I Human chr8 + 85213385 85213385 85213385 AACATGGTGAAACCCCATCTCTATAAAAAAATAAAAAAAATGAGCCGGTCGTGGTGGCAGGCACC AACATGGTGAAACCCCATCTCTATAAAAAAATTAAAAAAATGAGCCGGTCGTGGTGGCAGGCACC A T E2F5 Ensembl:ENSG00000133740 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985855977 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_180780 46385 RMVar_ID_46385 Human_SNP_ID_371452101 A-to-I Human chr8 + 85281530 85281530 85281530 AGATCTCTCTCTCTTTTTTTTTTATTTTTTTTAGTGATAGAGTCTCACTCTGTCACCCAGGCTGG AGATCTCTCTCTCTTTTTTTTTTATTTTTTTTTGTGATAGAGTCTCACTCTGTCACCCAGGCTGG A T CA13 Ensembl:ENSG00000185015 Protein coding 3'UTR GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1453370534 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7879369 RMVar_hsa_circ_252891,RMVar_hsa_circ_265657 46386 RMVar_ID_46386 Human_SNP_ID_371700915 A-to-I Human chr8 + 86394583 86394583 86394583 ATGAGCAAAGCAGTGGTAAGGAGGTCTCCTTTAGGCTAGTCAAGGTTTGTCCTGCTTCTTCCCCA ATGAGCAAAGCAGTGGTAAGGAGGTCTCCTTTGGGCTAGTCAAGGTTTGTCCTGCTTCTTCCCCA A G WWP1 Ensembl:ENSG00000123124 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1464330397 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1855,RMVar_hsa_circ_127896,RMVar_hsa_circ_93488,RMVar_hsa_circ_298904,RMVar_hsa_circ_252892,RMVar_hsa_circ_309466,RMVar_hsa_circ_94832,RMVar_hsa_circ_252894,RMVar_hsa_circ_64317,RMVar_hsa_circ_252895,RMVar_hsa_circ_252896,RMVar_hsa_circ_102999,RMVar_hsa_circ_314218,RMVar_hsa_circ_320172,RMVar_hsa_circ_69564,RMVar_hsa_circ_252902,RMVar_hsa_circ_112416,RMVar_hsa_circ_252899,RMVar_hsa_circ_252900,RMVar_hsa_circ_252898,RMVar_hsa_circ_322942,RMVar_hsa_circ_362041,RMVar_hsa_circ_377546,RMVar_hsa_circ_295388,RMVar_hsa_circ_252904,RMVar_hsa_circ_252903,RMVar_hsa_circ_64318,RMVar_hsa_circ_368095,RMVar_hsa_circ_252901,RMVar_hsa_circ_305489,RMVar_hsa_circ_74623,RMVar_hsa_circ_39655,RMVar_hsa_circ_45171,RMVar_hsa_circ_252907 46387 RMVar_ID_46387 Human_SNP_ID_371704482 A-to-I Human chr8 + 86409392 86409392 86409392 AGTAGCTGGGATTACAGGCACACAACCACCACACCCAGCTAATTTTCCTATTTTTTGGTAGAGAC AGTAGCTGGGATTACAGGCACACAACCACCACTCCCAGCTAATTTTCCTATTTTTTGGTAGAGAC A T WWP1 Ensembl:ENSG00000123124 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1290788028 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1855,RMVar_hsa_circ_93488,RMVar_hsa_circ_309466,RMVar_hsa_circ_94832,RMVar_hsa_circ_64317,RMVar_hsa_circ_252895,RMVar_hsa_circ_252896,RMVar_hsa_circ_102999,RMVar_hsa_circ_314218,RMVar_hsa_circ_3736,RMVar_hsa_circ_252902,RMVar_hsa_circ_112416,RMVar_hsa_circ_252899,RMVar_hsa_circ_252900,RMVar_hsa_circ_362041,RMVar_hsa_circ_377546,RMVar_hsa_circ_64318,RMVar_hsa_circ_368095,RMVar_hsa_circ_252901,RMVar_hsa_circ_74623,RMVar_hsa_circ_39655,RMVar_hsa_circ_45171,RMVar_hsa_circ_69935,RMVar_hsa_circ_307488,RMVar_hsa_circ_58558,RMVar_hsa_circ_102694,RMVar_hsa_circ_338682,RMVar_hsa_circ_45988,RMVar_hsa_circ_53875,RMVar_hsa_circ_27554,RMVar_hsa_circ_252911 46388 RMVar_ID_46388 Human_SNP_ID_371717540 A-to-I Human chr8 + 86463486 86463486 86463486 GCACCACCACGCCCAGCTAATTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGTCAGGC GCACCACCACGCCCAGCTAATTTTGTATTTTTGGTAGAGATGGGGTTTCACCATGTTGGTCAGGC A G WWP1 Ensembl:ENSG00000123124 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1230519111 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86757,RMVar_hsa_circ_252917 46389 RMVar_ID_46389 Human_SNP_ID_371717563 A-to-I Human chr8 + 86463566 86463566 86463566 CTCACCTTGTGATCTGCCCGCCTTGGCCTCGCAAAGTGCTGGGATTACAGGCGTGAGCCACCATG CTCACCTTGTGATCTGCCCGCCTTGGCCTCGCCAAGTGCTGGGATTACAGGCGTGAGCCACCATG A C WWP1 Ensembl:ENSG00000123124 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs960498740 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86757,RMVar_hsa_circ_252917 46390 RMVar_ID_46390 Human_SNP_ID_371717564 A-to-I Human chr8 + 86463566 86463566 86463566 CTCACCTTGTGATCTGCCCGCCTTGGCCTCGCAAAGTGCTGGGATTACAGGCGTGAGCCACCATG CTCACCTTGTGATCTGCCCGCCTTGGCCTCGCGAAGTGCTGGGATTACAGGCGTGAGCCACCATG A G WWP1 Ensembl:ENSG00000123124 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs960498740 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86757,RMVar_hsa_circ_252917 46391 RMVar_ID_46391 Human_SNP_ID_371718035 A-to-I Human chr8 + 86465495 86465495 86465495 AAAAAATACAAAAGTTAGCTGGCCATGGTGGCATGCGCCTGTACTCCCAGCCACTCCAGGGACTG AAAAAATACAAAAGTTAGCTGGCCATGGTGGCGTGCGCCTGTACTCCCAGCCACTCCAGGGACTG A G WWP1 Ensembl:ENSG00000123124 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1176132192 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86757,RMVar_hsa_circ_252917 46392 RMVar_ID_46392 Human_SNP_ID_371722367 A-to-I Human chr8 - 86482026 86482026 86482026 CAGGAGGACCAGTGATTAGCATTTACGATGCAAAGACAGAACAACTTCGTATAGGACTGTACTCC CAGGAGGACCAGTGATTAGCATTTACGATGCAGAGACAGAACAACTTCGTATAGGACTGTACTCC T C NTAN1P2,RMDN1 Ensembl:ENSG00000250569,Ensembl:ENSG00000176623 Pseudogene,Protein coding exon,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1204764110 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8155977,Human_RBP_ID_16485249 RMVar_hsa_circ_252930,RMVar_hsa_circ_322719,RMVar_hsa_circ_326423,RMVar_hsa_circ_252931,RMVar_hsa_circ_252933,RMVar_hsa_circ_338284,RMVar_hsa_circ_252932,RMVar_hsa_circ_337516 46393 RMVar_ID_46393 Human_SNP_ID_371722505 A-to-I Human chr8 + 86482577 86482577 86482577 ATCTTCTTGCCTGTCAAATTCACTAAGAAGTTAATGAGTGAGTTTTTGTGACAACTGCCTCCCAC ATCTTCTTGCCTGTCAAATTCACTAAGAAGTTCATGAGTGAGTTTTTGTGACAACTGCCTCCCAC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs961504680 Functional Loss SNV dbSNP153 33..33 33 - - - 46394 RMVar_ID_46394 Human_SNP_ID_371722506 A-to-I Human chr8 + 86482577 86482577 86482577 ATCTTCTTGCCTGTCAAATTCACTAAGAAGTTAATGAGTGAGTTTTTGTGACAACTGCCTCCCAC ATCTTCTTGCCTGTCAAATTCACTAAGAAGTTGATGAGTGAGTTTTTGTGACAACTGCCTCCCAC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs961504680 Functional Loss SNV dbSNP153 33..33 33 - - - 46395 RMVar_ID_46395 Human_SNP_ID_371722507 A-to-I Human chr8 + 86482577 86482577 86482577 ATCTTCTTGCCTGTCAAATTCACTAAGAAGTTAATGAGTGAGTTTTTGTGACAACTGCCTCCCAC ATCTTCTTGCCTGTCAAATTCACTAAGAAGTTTATGAGTGAGTTTTTGTGACAACTGCCTCCCAC A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs961504680 Functional Loss SNV dbSNP153 33..33 33 - - - 46396 RMVar_ID_46396 Human_SNP_ID_371727910 A-to-I Human chr8 + 86504070 86504070 86504070 TTGGCACTCTCAACCAGCTGGGCATCATTGTCAGAATTCTGGTGGCCCAGATCTTTGGTCTGGAA TTGGCACTCTCAACCAGCTGGGCATCATTGTCGGAATTCTGGTGGCCCAGATCTTTGGTCTGGAA A G SLC2A3P4 Ensembl:ENSG00000254088 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1258624474 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8274225 46397 RMVar_ID_46397 Human_SNP_ID_371727955 A-to-I Human chr8 + 86504266 86504266 86504266 AGAAGAGGAGAATGCTAAGTAGATCCTCCAGCAGTTGTGGGGCACCCAGGATGTATCCCAAGACA AGAAGAGGAGAATGCTAAGTAGATCCTCCAGCGGTTGTGGGGCACCCAGGATGTATCCCAAGACA A G SLC2A3P4 Ensembl:ENSG00000254088 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs990686357 Functional Loss SNV dbSNP153 33..33 33 - - - 46398 RMVar_ID_46398 Human_SNP_ID_371742060 A-to-I Human chr8 + 86561204 86561204 86561204 TTTTGTAAACTTCCTGGAAAGCTGTCTTCACTAAGTATCCCCTAGTCTCTATATATGTGGTTAGT TTTTGTAAACTTCCTGGAAAGCTGTCTTCACTGAGTATCCCCTAGTCTCTATATATGTGGTTAGT A G CPNE3 Ensembl:ENSG00000085719 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1563706186 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_705241,Human_RBP_ID_7862466,Human_RBP_ID_8221966,Human_RBP_ID_8922166,Human_RBP_ID_17319782,Human_RBP_ID_17433543,Human_RBP_ID_17546844,Human_RBP_ID_18393074,Human_RBP_ID_24270537,Human_RBP_ID_24441775,Human_RBP_ID_27779954 RMVar_hsa_circ_252945,RMVar_hsa_circ_104749,RMVar_hsa_circ_95304,RMVar_hsa_circ_107357,RMVar_hsa_circ_252946,RMVar_hsa_circ_252950,RMVar_hsa_circ_75933,RMVar_hsa_circ_252953 46399 RMVar_ID_46399 Human_SNP_ID_371765900 A-to-I Human chr8 - 86658051 86658051 86658051 CCTGCAGGGGGCCATGGAGAAGCTGCAGAGCCACTTTATGGAGCTCATGCAGGAGAAGGTGGACC CCTGCAGGGGGCCATGGAGAAGCTGCAGAGCCGCTTTATGGAGCTCATGCAGGAGAAGGTGGACC T C GOLGA2P1,CNGB3 Ensembl:ENSG00000205333,Ensembl:ENSG00000170289 Pseudogene,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1033736329 Functional Loss SNV dbSNP153 33..33 33 - - - 46400 RMVar_ID_46400 Human_SNP_ID_371766855 A-to-I Human chr8 - 86661830 86661830 86661830 GACATCAGTTCTGGAACGTCCAGAAGATACTGAGAACAACAATTACCTTCGTCAGCAATTGAAGT GACATCAGTTCTGGAACGTCCAGAAGATACTGTGAACAACAATTACCTTCGTCAGCAATTGAAGT T A UBE2Q2P10,CNGB3 Ensembl:ENSG00000233915,Ensembl:ENSG00000170289 Pseudogene,Protein coding exon,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1273974019 Functional Loss SNV dbSNP153 33..33 33 - - - 46401 RMVar_ID_46401 Human_SNP_ID_372577574 A-to-I Human chr8 - 89749733 89749733 89749733 AAGAGAATGCTTTCATATTTTCCTCATTCAGTATGATACTGGCTGTTGGTTTGGCATACATGGCT AAGAGAATGCTTTCATATTTTCCTCATTCAGTGTGATACTGGCTGTTGGTTTGGCATACATGGCT T C AF117829.1 Ensembl:ENSG00000251136 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1204286910 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5270862,Human_RBP_ID_8274455,Human_RBP_ID_16486786 46402 RMVar_ID_46402 Human_SNP_ID_546794335 A-to-I Human chr14 - 19099141 19099141 19099141 CTGCTAGGGAATGAATCCCCATCCCAGGAGGAAGGCGTGGCGGGGACGGAAGAAACAACCACACG CTGCTAGGGAATGAATCCCCATCCCAGGAGGAGGGCGTGGCGGGGACGGAAGAAACAACCACACG T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs75585527 Functional Loss SNV dbSNP153 33..33 33 - - - 46403 RMVar_ID_46403 Human_SNP_ID_547119907 A-to-I Human chr14 - 20270705 20270705 20270705 CCTCTGCTGAGTTTCAGACTTGTTTGGGAACTATTACCCCTTTCTTTTGGCCAATTTCTCCCTTT CCTCTGCTGAGTTTCAGACTTGTTTGGGAACTGTTACCCCTTTCTTTTGGCCAATTTCTCCCTTT T C TTC5 Ensembl:ENSG00000136319 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs916700781 Functional Loss SNV dbSNP153 33..33 33 - - - 46404 RMVar_ID_46404 Human_SNP_ID_547119934 A-to-I Human chr14 - 20270830 20270830 20270830 ACCTTGCAAAGCCACAGGGGCAGAGCTGCCCAAGACCTTGGGAGCCAATCTTTTGCATCAGTATG ACCTTGCAAAGCCACAGGGGCAGAGCTGCCCAGGACCTTGGGAGCCAATCTTTTGCATCAGTATG T C TTC5 Ensembl:ENSG00000136319 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971869306 Functional Loss SNV dbSNP153 33..33 33 - - - 46405 RMVar_ID_46405 Human_SNP_ID_547120033 A-to-I Human chr14 - 20271167 20271165 20271167 GCCATAAGCCTTGGTGGCCTCCATGTTTTGTTAAGTCTGTGAGCATATGGATTGCAAGAGTGAAG GCCATAAGCCTTGGTGGCCTCCATGTTTTGTT__GTCTGTGAGCATATGGATTGCAAGAGTGAAG CTT C TTC5 Ensembl:ENSG00000136319 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs915105102 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_3443471 46406 RMVar_ID_46406 Human_SNP_ID_547120081 A-to-I Human chr14 - 20271321 20271321 20271321 AGGAAGAAAGAATGGTTTCGTGGGCCAGTCCCAGAGTACTGCTGCCCTGTGCAGCTTTGTGACAG AGGAAGAAAGAATGGTTTCGTGGGCCAGTCCCGGAGTACTGCTGCCCTGTGCAGCTTTGTGACAG T C TTC5 Ensembl:ENSG00000136319 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs958077633 Functional Loss SNV dbSNP153 33..33 33 - - - 46407 RMVar_ID_46407 Human_SNP_ID_547120587 A-to-I Human chr14 - 20273304 20273304 20273304 GGCTGCTTTCATGGGCTGGCATTGAGTGTGCAAGCTGCTGGTGGATCTGCCATTCTGGGATCTGG GGCTGCTTTCATGGGCTGGCATTGAGTGTGCATGCTGCTGGTGGATCTGCCATTCTGGGATCTGG T A TTC5 Ensembl:ENSG00000136319 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs955403175 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19919596 46408 RMVar_ID_46408 Human_SNP_ID_547120588 A-to-I Human chr14 - 20273304 20273304 20273304 GGCTGCTTTCATGGGCTGGCATTGAGTGTGCAAGCTGCTGGTGGATCTGCCATTCTGGGATCTGG GGCTGCTTTCATGGGCTGGCATTGAGTGTGCACGCTGCTGGTGGATCTGCCATTCTGGGATCTGG T G TTC5 Ensembl:ENSG00000136319 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs955403175 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_19919596 46409 RMVar_ID_46409 Human_SNP_ID_547120613 A-to-I Human chr14 - 20273377 20273377 20273377 GATGCAAGAGGTGGGCTCCCACAGCCTTGGGAAGGTCTGCCCCTGTGGTTTTGCAGGGTAAAGCC GATGCAAGAGGTGGGCTCCCACAGCCTTGGGAGGGTCTGCCCCTGTGGTTTTGCAGGGTAAAGCC T C TTC5 Ensembl:ENSG00000136319 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs919926255 Functional Loss SNV dbSNP153 33..33 33 - - - 46410 RMVar_ID_46410 Human_SNP_ID_547120679 A-to-I Human chr14 - 20273584 20273584 20273584 CTGTAAAATCAAAAGGAAGTTAGTTACTTCCTAGATAGAATGTGGGTACAGGCATTGAGTAAATA CTGTAAAATCAAAAGGAAGTTAGTTACTTCCTGGATAGAATGTGGGTACAGGCATTGAGTAAATA T C TTC5 Ensembl:ENSG00000136319 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs769856146 Functional Loss SNV dbSNP153 33..33 33 - - - 46411 RMVar_ID_46411 Human_SNP_ID_547120712 A-to-I Human chr14 - 20273704 20273704 20273704 AACCGAATCATGCCCTTCCAATAGTCCCCCAAAGTCTTAACCCATTTCAGAGTTAACTCAAAAGT AACCGAATCATGCCCTTCCAATAGTCCCCCAAGGTCTTAACCCATTTCAGAGTTAACTCAAAAGT T C TTC5 Ensembl:ENSG00000136319 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1308991586 Functional Loss SNV dbSNP153 33..33 33 - - - 46412 RMVar_ID_46412 Human_SNP_ID_547133157 A-to-I Human chr14 - 20316997 20316997 20316997 TCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTAGAGGCTTGAATCACCACGCCTG TCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTGGCTGGGATTAGAGGCTTGAATCACCACGCCTG T C CCNB1IP1 Ensembl:ENSG00000100814 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs776762351 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6330066,Human_RBP_ID_25086705 RMVar_hsa_circ_98449,RMVar_hsa_circ_62517,RMVar_hsa_circ_297007,RMVar_hsa_circ_330001,RMVar_hsa_circ_165046,RMVar_hsa_circ_165048 46413 RMVar_ID_46413 Human_SNP_ID_547133236 A-to-I Human chr14 - 20317242 20317242 20317242 GCCACCACACCCAGCTAATTTTTTGTATTTTTAGTAGAGATGGGATTTCACCATGTTAGGCTGGT GCCACCACACCCAGCTAATTTTTTGTATTTTTTGTAGAGATGGGATTTCACCATGTTAGGCTGGT T A CCNB1IP1 Ensembl:ENSG00000100814 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167148352 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98449,RMVar_hsa_circ_62517,RMVar_hsa_circ_297007,RMVar_hsa_circ_330001,RMVar_hsa_circ_165046,RMVar_hsa_circ_165048 46414 RMVar_ID_46414 Human_SNP_ID_547133571 A-to-I Human chr14 - 20318217 20318217 20318217 TGCCCGCCTCAGCCTCCCAAAGTGTTGGGATTACAGGCGTGAGCCACCGCGCCCGGCCCACTATC TGCCCGCCTCAGCCTCCCAAAGTGTTGGGATTGCAGGCGTGAGCCACCGCGCCCGGCCCACTATC T C CCNB1IP1 Ensembl:ENSG00000100814 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1164597625 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98449,RMVar_hsa_circ_62517,RMVar_hsa_circ_297007,RMVar_hsa_circ_330001,RMVar_hsa_circ_165046,RMVar_hsa_circ_165048 46415 RMVar_ID_46415 Human_SNP_ID_547133772 A-to-I Human chr14 - 20318989 20318989 20318989 GGAGGCCGAGGTGGGTGGATCACTGGAGGTCAATAGTTTGAAACCAGCTTGGCCAACATGGCGAG GGAGGCCGAGGTGGGTGGATCACTGGAGGTCAGTAGTTTGAAACCAGCTTGGCCAACATGGCGAG T C CCNB1IP1 Ensembl:ENSG00000100814 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs942759604 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98449,RMVar_hsa_circ_62517,RMVar_hsa_circ_297007,RMVar_hsa_circ_330001,RMVar_hsa_circ_165046,RMVar_hsa_circ_165048 46416 RMVar_ID_46416 Human_SNP_ID_547133785 A-to-I Human chr14 - 20319035 20319035 20319035 TATAAGGCTGGGCATGGTGGCGCACGCCTGTAATCCCGGCACGTTGGGAGGCCGAGGTGGGTGGA TATAAGGCTGGGCATGGTGGCGCACGCCTGTACTCCCGGCACGTTGGGAGGCCGAGGTGGGTGGA T G CCNB1IP1 Ensembl:ENSG00000100814 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1168891218 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1487562 RMVar_hsa_circ_98449,RMVar_hsa_circ_62517,RMVar_hsa_circ_297007,RMVar_hsa_circ_330001,RMVar_hsa_circ_165046,RMVar_hsa_circ_165048 46417 RMVar_ID_46417 Human_SNP_ID_547134162 A-to-I Human chr14 - 20320718 20320718 20320718 TCACTGCAACCTCCGCCTCCCGGGTTCAGGCTATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGA TCACTGCAACCTCCGCCTCCCGGGTTCAGGCTGTTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGA T C CCNB1IP1 Ensembl:ENSG00000100814 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs573005840 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98449,RMVar_hsa_circ_62517,RMVar_hsa_circ_297007,RMVar_hsa_circ_330001,RMVar_hsa_circ_165046,RMVar_hsa_circ_165048 46418 RMVar_ID_46418 Human_SNP_ID_547134652 A-to-I Human chr14 - 20322696 20322696 20322696 ATCGCTTGAACCCGGGAGGTGGAGATTGTAGTAAGCCGCGATTGTGCCACTGCACTCCAGCCTGG ATCGCTTGAACCCGGGAGGTGGAGATTGTAGTGAGCCGCGATTGTGCCACTGCACTCCAGCCTGG T C CCNB1IP1 Ensembl:ENSG00000100814 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1423943097 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12290301 RMVar_hsa_circ_98449,RMVar_hsa_circ_62517,RMVar_hsa_circ_297007,RMVar_hsa_circ_330001,RMVar_hsa_circ_165046,RMVar_hsa_circ_165048 46419 RMVar_ID_46419 Human_SNP_ID_547134846 A-to-I Human chr14 - 20323557 20323557 20323557 ATTTTTTTTTTTTTGAGACAGGGACTCATTCCATTGCCCAGGCTGGAGTGCAGTGGCATAATCAG ATTTTTTTTTTTTTGAGACAGGGACTCATTCCGTTGCCCAGGCTGGAGTGCAGTGGCATAATCAG T C CCNB1IP1 Ensembl:ENSG00000100814 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1229067240 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6330116,Human_RBP_ID_12290331 RMVar_hsa_circ_98449,RMVar_hsa_circ_62517,RMVar_hsa_circ_297007,RMVar_hsa_circ_330001,RMVar_hsa_circ_165046,RMVar_hsa_circ_165048 46420 RMVar_ID_46420 Human_SNP_ID_547135067 A-to-I Human chr14 - 20324220 20324218 20324220 ATCGCACCACTGCACTCCAGCTTGGGTGACAGAGCTAGACTTCGTCTCAGAAAAAAAGAGGAAAT ATCGCACCACTGCACTCCAGCTTGGGTGACAG__CTAGACTTCGTCTCAGAAAAAAAGAGGAAAT GCT G CCNB1IP1 Ensembl:ENSG00000100814 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs778811997 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_98449,RMVar_hsa_circ_62517,RMVar_hsa_circ_297007,RMVar_hsa_circ_330001,RMVar_hsa_circ_165046,RMVar_hsa_circ_165048 46421 RMVar_ID_46421 Human_SNP_ID_547135084 A-to-I Human chr14 - 20324292 20324292 20324292 ATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAATCTGGGAGGCAGAGGTTGTGGTG ATCCCAGCTACTTGGGAGGCTGAGGCAGGAGATTCGCTTGAATCTGGGAGGCAGAGGTTGTGGTG T A CCNB1IP1 Ensembl:ENSG00000100814 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1394754520 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98449,RMVar_hsa_circ_62517,RMVar_hsa_circ_297007,RMVar_hsa_circ_330001,RMVar_hsa_circ_165046,RMVar_hsa_circ_165048 46422 RMVar_ID_46422 Human_SNP_ID_547135085 A-to-I Human chr14 - 20324315 20324315 20324315 GGGTGTGGTGGCGTGCACCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAA GGGTGTGGTGGCGTGCACCTGTAATCCCAGCTGCTTGGGAGGCTGAGGCAGGAGAATCGCTTGAA T C CCNB1IP1 Ensembl:ENSG00000100814 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1388923845 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98449,RMVar_hsa_circ_62517,RMVar_hsa_circ_297007,RMVar_hsa_circ_330001,RMVar_hsa_circ_165046,RMVar_hsa_circ_165048 46423 RMVar_ID_46423 Human_SNP_ID_547135095 A-to-I Human chr14 - 20324351 20324351 20324351 GAAACCTCGTTTCTACCAAAAATACAAAAATTAGCTGGGTGTGGTGGCGTGCACCTGTAATCCCA GAAACCTCGTTTCTACCAAAAATACAAAAATTGGCTGGGTGTGGTGGCGTGCACCTGTAATCCCA T C CCNB1IP1 Ensembl:ENSG00000100814 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1343380953 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98449,RMVar_hsa_circ_62517,RMVar_hsa_circ_297007,RMVar_hsa_circ_330001,RMVar_hsa_circ_165046,RMVar_hsa_circ_165048 46424 RMVar_ID_46424 Human_SNP_ID_547135113 A-to-I Human chr14 - 20324429 20324429 20324429 GTAAACCCAGCACTTTGGGAGGCGAGGTGGGCAGATCACCTAAGGTCAGGAGTTCAAGACCAGCC GTAAACCCAGCACTTTGGGAGGCGAGGTGGGCGGATCACCTAAGGTCAGGAGTTCAAGACCAGCC T C CCNB1IP1 Ensembl:ENSG00000100814 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1458682802 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98449,RMVar_hsa_circ_62517,RMVar_hsa_circ_297007,RMVar_hsa_circ_330001,RMVar_hsa_circ_165046,RMVar_hsa_circ_165048 46425 RMVar_ID_46425 Human_SNP_ID_547135265 A-to-I Human chr14 - 20324984 20324984 20324984 ACATGGCAAAACCCCATCTCTACTAAAAAAATACAAAAAATTATCTGGGCCTGGTGGTGTGCGCC ACATGGCAAAACCCCATCTCTACTAAAAAAATTCAAAAAATTATCTGGGCCTGGTGGTGTGCGCC T A CCNB1IP1 Ensembl:ENSG00000100814 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs896664975 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98449,RMVar_hsa_circ_62517,RMVar_hsa_circ_297007,RMVar_hsa_circ_330001,RMVar_hsa_circ_165046,RMVar_hsa_circ_165048 46426 RMVar_ID_46426 Human_SNP_ID_547135266 A-to-I Human chr14 - 20324984 20324984 20324984 ACATGGCAAAACCCCATCTCTACTAAAAAAATACAAAAAATTATCTGGGCCTGGTGGTGTGCGCC ACATGGCAAAACCCCATCTCTACTAAAAAAATCCAAAAAATTATCTGGGCCTGGTGGTGTGCGCC T G CCNB1IP1 Ensembl:ENSG00000100814 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs896664975 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98449,RMVar_hsa_circ_62517,RMVar_hsa_circ_297007,RMVar_hsa_circ_330001,RMVar_hsa_circ_165046,RMVar_hsa_circ_165048 46427 RMVar_ID_46427 Human_SNP_ID_547135289 A-to-I Human chr14 - 20325092 20325092 20325092 AAAGTCAGTTGAGGCCAGGCGTGGTGGCTCACACCTGTAATCCTAGCACTTTGGGAGGCCGAGGT AAAGTCAGTTGAGGCCAGGCGTGGTGGCTCACGCCTGTAATCCTAGCACTTTGGGAGGCCGAGGT T C CCNB1IP1 Ensembl:ENSG00000100814 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs954479208 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98449,RMVar_hsa_circ_62517,RMVar_hsa_circ_297007,RMVar_hsa_circ_330001,RMVar_hsa_circ_165046,RMVar_hsa_circ_165048 46428 RMVar_ID_46428 Human_SNP_ID_547141605 A-to-I Human chr14 + 20347977 20347977 20347977 CCCACTGCAACCTTGAACTTCTGGGCTCCAGCAATCCTCCCACCTAAGCTTCCTGAGTAGCTCGG CCCACTGCAACCTTGAACTTCTGGGCTCCAGCGATCCTCCCACCTAAGCTTCCTGAGTAGCTCGG A G PARP2 Ensembl:ENSG00000129484 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs942530961 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41350,RMVar_hsa_circ_165083,RMVar_hsa_circ_301610,RMVar_hsa_circ_165080,RMVar_hsa_circ_356654,RMVar_hsa_circ_319875,RMVar_hsa_circ_165082,RMVar_hsa_circ_341571,RMVar_hsa_circ_109053,RMVar_hsa_circ_165085,RMVar_hsa_circ_165084,RMVar_hsa_circ_321416,RMVar_hsa_circ_165087 46429 RMVar_ID_46429 Human_SNP_ID_547146356 A-to-I Human chr14 - 20366218 20366218 20366218 CTGGAGTGAAGGGGTTGGGGAAAGTTAAGCAAAGGCTAACTTGACCAATAGGCTCAATAGATTCA CTGGAGTGAAGGGGTTGGGGAAAGTTAAGCAACGGCTAACTTGACCAATAGGCTCAATAGATTCA T G TEP1 Ensembl:ENSG00000129566 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1447627490 Functional Loss SNV dbSNP153 33..33 33 - - - 46430 RMVar_ID_46430 Human_SNP_ID_547146357 A-to-I Human chr14 - 20366229 20366229 20366229 CCCAGCTAAGGCTGGAGTGAAGGGGTTGGGGAAAGTTAAGCAAAGGCTAACTTGACCAATAGGCT CCCAGCTAAGGCTGGAGTGAAGGGGTTGGGGAGAGTTAAGCAAAGGCTAACTTGACCAATAGGCT T C TEP1 Ensembl:ENSG00000129566 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs11555905 Functional Loss SNV dbSNP153 33..33 33 - - - 46431 RMVar_ID_46431 Human_SNP_ID_547146365 A-to-I Human chr14 - 20366268 20366268 20366268 TTGTCTCTCTTCCATGCTCTGAAAATTATATAAAAGCATCCCAGCTAAGGCTGGAGTGAAGGGGT TTGTCTCTCTTCCATGCTCTGAAAATTATATACAAGCATCCCAGCTAAGGCTGGAGTGAAGGGGT T G TEP1 Ensembl:ENSG00000129566 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1343613411 Functional Loss SNV dbSNP153 33..33 33 - - - 46432 RMVar_ID_46432 Human_SNP_ID_547146368 A-to-I Human chr14 - 20366273 20366272 20366273 TCTATTTGTCTCTCTTCCATGCTCTGAAAATTATATAAAAGCATCCCAGCTAAGGCTGGAGTGAA TCTATTTGTCTCTCTTCCATGCTCTGAAAATT_TATAAAAGCATCCCAGCTAAGGCTGGAGTGAA AT A TEP1 Ensembl:ENSG00000129566 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1322246666 Functional Loss DEL dbSNP153 33..33 33 - - - 46433 RMVar_ID_46433 Human_SNP_ID_547146369 A-to-I Human chr14 - 20366277 20366277 20366277 AAGCTCTATTTGTCTCTCTTCCATGCTCTGAAAATTATATAAAAGCATCCCAGCTAAGGCTGGAG AAGCTCTATTTGTCTCTCTTCCATGCTCTGAAGATTATATAAAAGCATCCCAGCTAAGGCTGGAG T C TEP1 Ensembl:ENSG00000129566 Protein coding 3'UTR GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs1403124858 Functional Loss SNV dbSNP153 33..33 33 - - - 46434 RMVar_ID_46434 Human_SNP_ID_547146372 A-to-I Human chr14 - 20366302 20366302 20366302 AAAATCTTGGGCCAATTGCAGGAGGAAGCTCTATTTGTCTCTCTTCCATGCTCTGAAAATTATAT AAAATCTTGGGCCAATTGCAGGAGGAAGCTCTGTTTGTCTCTCTTCCATGCTCTGAAAATTATAT T C TEP1 Ensembl:ENSG00000129566 Protein coding 3'UTR GSE47997;GSE38233;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;cultured B-cells;HepG2 cell line - 23474544,24183664,24183664,29129909 RNA-Seq:(High) rs1164201559 Functional Loss SNV dbSNP153 33..33 33 - - - 46435 RMVar_ID_46435 Human_SNP_ID_547146374 A-to-I Human chr14 - 20366308 20366308 20366308 TCCCCTAAAATCTTGGGCCAATTGCAGGAGGAAGCTCTATTTGTCTCTCTTCCATGCTCTGAAAA TCCCCTAAAATCTTGGGCCAATTGCAGGAGGAGGCTCTATTTGTCTCTCTTCCATGCTCTGAAAA T C TEP1 Ensembl:ENSG00000129566 Protein coding 3'UTR GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs1388138074 Functional Loss SNV dbSNP153 33..33 33 - - - 46436 RMVar_ID_46436 Human_SNP_ID_547146384 A-to-I Human chr14 - 20366333 20366330 20366333 TTGATTTCAATCTTTTGCCTTTTGCTCCCCTAAAATCTTGGGCCAATTGCAGGAGGAAGCTCTAT TTGATTTCAATCTTTTGCCTTTTGCTCCCCTA___TCTTGGGCCAATTGCAGGAGGAAGCTCTAT ATTT A TEP1 Ensembl:ENSG00000129566 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1453417664 Functional Loss DEL dbSNP153 33..35 33 - - - 46437 RMVar_ID_46437 Human_SNP_ID_547146390 A-to-I Human chr14 - 20366356 20366356 20366356 ATGGCATGGCATCATCCTAGTCATTGATTTCAATCTTTTGCCTTTTGCTCCCCTAAAATCTTGGG ATGGCATGGCATCATCCTAGTCATTGATTTCATTCTTTTGCCTTTTGCTCCCCTAAAATCTTGGG T A TEP1 Ensembl:ENSG00000129566 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1247823702 Functional Loss SNV dbSNP153 33..33 33 - - - 46438 RMVar_ID_46438 Human_SNP_ID_547146391 A-to-I Human chr14 - 20366356 20366356 20366356 ATGGCATGGCATCATCCTAGTCATTGATTTCAATCTTTTGCCTTTTGCTCCCCTAAAATCTTGGG ATGGCATGGCATCATCCTAGTCATTGATTTCAGTCTTTTGCCTTTTGCTCCCCTAAAATCTTGGG T C TEP1 Ensembl:ENSG00000129566 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1247823702 Functional Loss SNV dbSNP153 33..33 33 - - - 46439 RMVar_ID_46439 Human_SNP_ID_547146458 A-to-I Human chr14 - 20366658 20366658 20366658 AAGACTTGGGGAGTTAAAGGGCACTGAGTTTTACTCTCACTGTACCCTGATTCCAGGTTTTACAT AAGACTTGGGGAGTTAAAGGGCACTGAGTTTTGCTCTCACTGTACCCTGATTCCAGGTTTTACAT T C TEP1 Ensembl:ENSG00000129566 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1760910 Functional Loss SNV dbSNP153 33..33 33 - - - 46440 RMVar_ID_46440 Human_SNP_ID_547146507 A-to-I Human chr14 - 20366936 20366936 20366936 TTGTAGAATTTTCAGAGCATGGGAGACAGACAACTAGAGCTTCCTCCTGCCCTTGGCCCATGCTT TTGTAGAATTTTCAGAGCATGGGAGACAGACAGCTAGAGCTTCCTCCTGCCCTTGGCCCATGCTT T C TEP1 Ensembl:ENSG00000129566 Protein coding 3'UTR GSE47997;GSE38233;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;cultured B-cells;HepG2 cell line - 23474544,24183664,24183664,29129909 RNA-Seq:(High) rs1289484659 Functional Loss SNV dbSNP153 33..33 33 - - - 46441 RMVar_ID_46441 Human_SNP_ID_547146508 A-to-I Human chr14 - 20366937 20366937 20366937 TTTGTAGAATTTTCAGAGCATGGGAGACAGACAACTAGAGCTTCCTCCTGCCCTTGGCCCATGCT TTTGTAGAATTTTCAGAGCATGGGAGACAGACGACTAGAGCTTCCTCCTGCCCTTGGCCCATGCT T C TEP1 Ensembl:ENSG00000129566 Protein coding 3'UTR GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs1224711399 Functional Loss SNV dbSNP153 33..33 33 - - - 46442 RMVar_ID_46442 Human_SNP_ID_547146511 A-to-I Human chr14 - 20366950 20366950 20366950 TTAGCTGGGGTGTTTTGTAGAATTTTCAGAGCATGGGAGACAGACAACTAGAGCTTCCTCCTGCC TTAGCTGGGGTGTTTTGTAGAATTTTCAGAGCGTGGGAGACAGACAACTAGAGCTTCCTCCTGCC T C TEP1 Ensembl:ENSG00000129566 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs576416008 Functional Loss SNV dbSNP153 33..33 33 - - - 46443 RMVar_ID_46443 Human_SNP_ID_547146517 A-to-I Human chr14 - 20366980 20366980 20366980 GCTTAACTTTCCTCCTCTGTTACTCCAGCCTTAGCTGGGGTGTTTTGTAGAATTTTCAGAGCATG GCTTAACTTTCCTCCTCTGTTACTCCAGCCTTGGCTGGGGTGTTTTGTAGAATTTTCAGAGCATG T C TEP1 Ensembl:ENSG00000129566 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1386271914 Functional Loss SNV dbSNP153 33..33 33 - - - 46444 RMVar_ID_46444 Human_SNP_ID_547146527 A-to-I Human chr14 - 20367031 20367031 20367031 TATTTCTAAAATTCAATCATATGGAAGAATCTATTGAGCAGGTTAGCCTTTGCTTAACTTTCCTC TATTTCTAAAATTCAATCATATGGAAGAATCTGTTGAGCAGGTTAGCCTTTGCTTAACTTTCCTC T C TEP1 Ensembl:ENSG00000129566 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1403881819 Functional Loss SNV dbSNP153 33..33 33 - - - 46445 RMVar_ID_46445 Human_SNP_ID_547146567 A-to-I Human chr14 - 20367181 20367181 20367181 TTTTTGTATTTCAGTAGAGACGAAGTTTCACCATGTTGGCCAGGTGGGTCTCAAACTCCTGACCT TTTTTGTATTTCAGTAGAGACGAAGTTTCACCCTGTTGGCCAGGTGGGTCTCAAACTCCTGACCT T G TEP1 Ensembl:ENSG00000129566 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs1242786303 Functional Loss SNV dbSNP153 33..33 33 - - - 46446 RMVar_ID_46446 Human_SNP_ID_547146602 A-to-I Human chr14 - 20367311 20367311 20367311 TCACCTAGGCTGGAGTGCAATGGTGCAATCTCAGCTCAGTGCAACCTCTGCTTCCTGGGTTCAAG TCACCTAGGCTGGAGTGCAATGGTGCAATCTCGGCTCAGTGCAACCTCTGCTTCCTGGGTTCAAG T C TEP1 Ensembl:ENSG00000129566 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs56327775 Functional Loss SNV dbSNP153 33..33 33 - - - 46447 RMVar_ID_46447 Human_SNP_ID_547146715 A-to-I Human chr14 - 20367650 20367650 20367650 GAGCCGAGACACCACTGCACTCCAGCCTGGGCAACAGAGCGAGACTCTGTCTAAAAAAAAAAAAA GAGCCGAGACACCACTGCACTCCAGCCTGGGCGACAGAGCGAGACTCTGTCTAAAAAAAAAAAAA T C TEP1 Ensembl:ENSG00000129566 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs140444610 Functional Loss SNV dbSNP153 33..33 33 - - - 46448 RMVar_ID_46448 Human_SNP_ID_547146716 A-to-I Human chr14 - 20367650 20367650 20367650 GAGCCGAGACACCACTGCACTCCAGCCTGGGCAACAGAGCGAGACTCTGTCTAAAAAAAAAAAAA GAGCCGAGACACCACTGCACTCCAGCCTGGGCCACAGAGCGAGACTCTGTCTAAAAAAAAAAAAA T G TEP1 Ensembl:ENSG00000129566 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs140444610 Functional Loss SNV dbSNP153 33..33 33 - - - 46449 RMVar_ID_46449 Human_SNP_ID_547146737 A-to-I Human chr14 - 20367737 20367737 20367737 AGGTGTGGCGGCGGGCACCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATGGCGTGAA AGGTGTGGCGGCGGGCACCTGTAGTCCCAGCTGCTTGGGAGGCTGAGGCAGGAGAATGGCGTGAA T C TEP1 Ensembl:ENSG00000129566 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs542208396 Functional Loss SNV dbSNP153 33..33 33 - - - 46450 RMVar_ID_46450 Human_SNP_ID_547146738 A-to-I Human chr14 - 20367737 20367737 20367737 AGGTGTGGCGGCGGGCACCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATGGCGTGAA AGGTGTGGCGGCGGGCACCTGTAGTCCCAGCTCCTTGGGAGGCTGAGGCAGGAGAATGGCGTGAA T G TEP1 Ensembl:ENSG00000129566 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs542208396 Functional Loss SNV dbSNP153 33..33 33 - - - 46451 RMVar_ID_46451 Human_SNP_ID_547146759 A-to-I Human chr14 - 20367810 20367810 20367810 GGTCAGGAGATCAAGACCATCCTGGCTAACATAGTGAAACCCTGTCTCTACTAAAAAATACAAAA GGTCAGGAGATCAAGACCATCCTGGCTAACATGGTGAAACCCTGTCTCTACTAAAAAATACAAAA T C TEP1 Ensembl:ENSG00000129566 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1387701725 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_121488 46452 RMVar_ID_46452 Human_SNP_ID_547154724 A-to-I Human chr14 - 20393668 20393668 20393668 CGTGCCTCAGACTCCCAAGTAGCTGGGATTACAGGTGCATACCACCACACCCCGCTAATTTTTGT CGTGCCTCAGACTCCCAAGTAGCTGGGATTACGGGTGCATACCACCACACCCCGCTAATTTTTGT T C TEP1 Ensembl:ENSG00000129566 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1289613208 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10328,RMVar_hsa_circ_113574,RMVar_hsa_circ_165090,RMVar_hsa_circ_111958,RMVar_hsa_circ_165093,RMVar_hsa_circ_121872,RMVar_hsa_circ_79556,RMVar_hsa_circ_165094,RMVar_hsa_circ_165095,RMVar_hsa_circ_26320,RMVar_hsa_circ_29601,RMVar_hsa_circ_65983 46453 RMVar_ID_46453 Human_SNP_ID_547154726 A-to-I Human chr14 - 20393670 20393670 20393670 CTCGTGCCTCAGACTCCCAAGTAGCTGGGATTACAGGTGCATACCACCACACCCCGCTAATTTTT CTCGTGCCTCAGACTCCCAAGTAGCTGGGATTGCAGGTGCATACCACCACACCCCGCTAATTTTT T C TEP1 Ensembl:ENSG00000129566 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs976285848 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10328,RMVar_hsa_circ_113574,RMVar_hsa_circ_165090,RMVar_hsa_circ_111958,RMVar_hsa_circ_165093,RMVar_hsa_circ_121872,RMVar_hsa_circ_79556,RMVar_hsa_circ_165094,RMVar_hsa_circ_165095,RMVar_hsa_circ_26320,RMVar_hsa_circ_29601,RMVar_hsa_circ_65983 46454 RMVar_ID_46454 Human_SNP_ID_547154759 A-to-I Human chr14 - 20393775 20393775 20393775 CCCTGGCTCTTTTTTTTTTTTTAATTGAGACAAAGTCCCACTTCGTCACCCAGGCTGGTGTGATC CCCTGGCTCTTTTTTTTTTTTTAATTGAGACAGAGTCCCACTTCGTCACCCAGGCTGGTGTGATC T C TEP1 Ensembl:ENSG00000129566 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs189583632 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10328,RMVar_hsa_circ_113574,RMVar_hsa_circ_165090,RMVar_hsa_circ_111958,RMVar_hsa_circ_165093,RMVar_hsa_circ_121872,RMVar_hsa_circ_79556,RMVar_hsa_circ_165094,RMVar_hsa_circ_165095,RMVar_hsa_circ_26320,RMVar_hsa_circ_29601,RMVar_hsa_circ_65983 46455 RMVar_ID_46455 Human_SNP_ID_547154825 A-to-I Human chr14 - 20394030 20394030 20394030 CAGGCTGGAGTGCAATGGCACAATCCCAGCTCACTGCAACCTCTACCTCTCAGGCTCAAGTGATT CAGGCTGGAGTGCAATGGCACAATCCCAGCTCCCTGCAACCTCTACCTCTCAGGCTCAAGTGATT T G TEP1 Ensembl:ENSG00000129566 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1383431044 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10328,RMVar_hsa_circ_113574,RMVar_hsa_circ_165090,RMVar_hsa_circ_111958,RMVar_hsa_circ_165093,RMVar_hsa_circ_121872,RMVar_hsa_circ_79556,RMVar_hsa_circ_165094,RMVar_hsa_circ_165095,RMVar_hsa_circ_26320,RMVar_hsa_circ_29601,RMVar_hsa_circ_65983 46456 RMVar_ID_46456 Human_SNP_ID_547154828 A-to-I Human chr14 - 20394048 20394048 20394048 GATTTTATTCCCATCACCCAGGCTGGAGTGCAATGGCACAATCCCAGCTCACTGCAACCTCTACC GATTTTATTCCCATCACCCAGGCTGGAGTGCAGTGGCACAATCCCAGCTCACTGCAACCTCTACC T C TEP1 Ensembl:ENSG00000129566 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs922661604 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10328,RMVar_hsa_circ_113574,RMVar_hsa_circ_165090,RMVar_hsa_circ_111958,RMVar_hsa_circ_165093,RMVar_hsa_circ_121872,RMVar_hsa_circ_79556,RMVar_hsa_circ_165094,RMVar_hsa_circ_165095,RMVar_hsa_circ_26320,RMVar_hsa_circ_29601,RMVar_hsa_circ_65983 46457 RMVar_ID_46457 Human_SNP_ID_547155737 A-to-I Human chr14 - 20397361 20397361 20397361 GGGATTAGAGGCACCAGACACCACGCCTGGCTAATTTTTGTATTTTTGTAGAGACGGGGTTTCAT GGGATTAGAGGCACCAGACACCACGCCTGGCTCATTTTTGTATTTTTGTAGAGACGGGGTTTCAT T G TEP1 Ensembl:ENSG00000129566 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1402059338 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113574,RMVar_hsa_circ_165090,RMVar_hsa_circ_60393,RMVar_hsa_circ_343573,RMVar_hsa_circ_29601,RMVar_hsa_circ_65983,RMVar_hsa_circ_104265,RMVar_hsa_circ_165098,RMVar_hsa_circ_165099,RMVar_hsa_circ_365169 46458 RMVar_ID_46458 Human_SNP_ID_547156538 A-to-I Human chr14 - 20400394 20400394 20400394 ATTTTAGAGACAAGGTCTTTGTAATGTTGCCCAGGCTGGTCTCAAACTCATGGCCTCAAGCATTT ATTTTAGAGACAAGGTCTTTGTAATGTTGCCCGGGCTGGTCTCAAACTCATGGCCTCAAGCATTT T C TEP1 Ensembl:ENSG00000129566 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1566477412 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113574,RMVar_hsa_circ_165090,RMVar_hsa_circ_60393,RMVar_hsa_circ_343573,RMVar_hsa_circ_29601,RMVar_hsa_circ_65983,RMVar_hsa_circ_104265,RMVar_hsa_circ_165098,RMVar_hsa_circ_165099,RMVar_hsa_circ_365169 46459 RMVar_ID_46459 Human_SNP_ID_547170536 A-to-I Human chr14 - 20450120 20450118 20450121 AGAATTGCTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCTGAGATCACGCCATTGCACTCCAGCC AGAATTGCTTGAACCTGGGAGGCAGAGGTTG___TGAGCTGAGATCACGCCATTGCACTCCAGCC ACTG A OSGEP Ensembl:ENSG00000092094 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1354956150 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_84879,RMVar_hsa_circ_128085,RMVar_hsa_circ_165106,RMVar_hsa_circ_165107,RMVar_hsa_circ_80529,RMVar_hsa_circ_165108,RMVar_hsa_circ_89325,RMVar_hsa_circ_119334,RMVar_hsa_circ_165109,RMVar_hsa_circ_165110 46460 RMVar_ID_46460 Human_SNP_ID_547170850 A-to-I Human chr14 - 20451389 20451389 20451389 GGCAGGAGAATCACTTGAACCCAGGAGGCGGAAGTTGCGGTGAACCGAGATCGCACCATTGCATT GGCAGGAGAATCACTTGAACCCAGGAGGCGGATGTTGCGGTGAACCGAGATCGCACCATTGCATT T A OSGEP Ensembl:ENSG00000092094 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs1395488597 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23306714 Human_Splice_Rec_1488322 RMVar_hsa_circ_84879,RMVar_hsa_circ_128085,RMVar_hsa_circ_165106,RMVar_hsa_circ_165107,RMVar_hsa_circ_80529,RMVar_hsa_circ_165108,RMVar_hsa_circ_89325,RMVar_hsa_circ_119334,RMVar_hsa_circ_165109,RMVar_hsa_circ_165110 46461 RMVar_ID_46461 Human_SNP_ID_547170855 A-to-I Human chr14 - 20451399 20451399 20451399 CCGGAGGCTGGGCAGGAGAATCACTTGAACCCAGGAGGCGGAAGTTGCGGTGAACCGAGATCGCA CCGGAGGCTGGGCAGGAGAATCACTTGAACCCGGGAGGCGGAAGTTGCGGTGAACCGAGATCGCA T C OSGEP Ensembl:ENSG00000092094 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs1278926492 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23306714 Human_Splice_Rec_1488322 RMVar_hsa_circ_84879,RMVar_hsa_circ_128085,RMVar_hsa_circ_165106,RMVar_hsa_circ_165107,RMVar_hsa_circ_80529,RMVar_hsa_circ_165108,RMVar_hsa_circ_89325,RMVar_hsa_circ_119334,RMVar_hsa_circ_165109,RMVar_hsa_circ_165110 46462 RMVar_ID_46462 Human_SNP_ID_547170879 A-to-I Human chr14 - 20451454 20451454 20451454 AAAAATAACAAAAATTAATTTGATGTGGTGGCAGGTGCCTGTAATCCTAGCAACTCCGGAGGCTG AAAAATAACAAAAATTAATTTGATGTGGTGGCGGGTGCCTGTAATCCTAGCAACTCCGGAGGCTG T C OSGEP Ensembl:ENSG00000092094 Protein coding intron GSE100210;GSE105773;GSE105773;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Glioblastoma cells,U87MG;Glioblastoma cells,U87MG;Bronchiolar epithelium,BEP2D cell line - 29129909,29724793,29724793,31158229 RNA-Seq:(High) rs1017290562 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25086920 RMVar_hsa_circ_84879,RMVar_hsa_circ_128085,RMVar_hsa_circ_165106,RMVar_hsa_circ_165107,RMVar_hsa_circ_80529,RMVar_hsa_circ_165108,RMVar_hsa_circ_89325,RMVar_hsa_circ_119334,RMVar_hsa_circ_165109,RMVar_hsa_circ_165110 46463 RMVar_ID_46463 Human_SNP_ID_547170898 A-to-I Human chr14 - 20451510 20451510 20451510 CTGAGGTCAGGAGTTTGAGCCCAGCCTGGCCAACGTGGCAAAACCCCATCTGTACTAAAAATAAC CTGAGGTCAGGAGTTTGAGCCCAGCCTGGCCAGCGTGGCAAAACCCCATCTGTACTAAAAATAAC T C OSGEP Ensembl:ENSG00000092094 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs927914081 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84879,RMVar_hsa_circ_128085,RMVar_hsa_circ_165106,RMVar_hsa_circ_165107,RMVar_hsa_circ_80529,RMVar_hsa_circ_165108,RMVar_hsa_circ_89325,RMVar_hsa_circ_119334,RMVar_hsa_circ_165109,RMVar_hsa_circ_165110 46464 RMVar_ID_46464 Human_SNP_ID_547170919 A-to-I Human chr14 - 20451580 20451580 20451580 AACAGTTGCTGGGTATGGCAACTCATGCCTGTAATTCCAGCACTTTGGGAGGTCGAGGCGGGTGG AACAGTTGCTGGGTATGGCAACTCATGCCTGTCATTCCAGCACTTTGGGAGGTCGAGGCGGGTGG T G OSGEP Ensembl:ENSG00000092094 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1395451920 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84879,RMVar_hsa_circ_128085,RMVar_hsa_circ_165106,RMVar_hsa_circ_165107,RMVar_hsa_circ_80529,RMVar_hsa_circ_165108,RMVar_hsa_circ_89325,RMVar_hsa_circ_119334,RMVar_hsa_circ_165109,RMVar_hsa_circ_165110 46465 RMVar_ID_46465 Human_SNP_ID_547170921 A-to-I Human chr14 - 20451592 20451592 20451592 GCAATTGAAACTAACAGTTGCTGGGTATGGCAACTCATGCCTGTAATTCCAGCACTTTGGGAGGT GCAATTGAAACTAACAGTTGCTGGGTATGGCAGCTCATGCCTGTAATTCCAGCACTTTGGGAGGT T C OSGEP Ensembl:ENSG00000092094 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1455671436 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84879,RMVar_hsa_circ_128085,RMVar_hsa_circ_165106,RMVar_hsa_circ_165107,RMVar_hsa_circ_80529,RMVar_hsa_circ_165108,RMVar_hsa_circ_89325,RMVar_hsa_circ_119334,RMVar_hsa_circ_165109,RMVar_hsa_circ_165110 46466 RMVar_ID_46466 Human_SNP_ID_547171455 A-to-I Human chr14 - 20453530 20453526 20453531 ACCATGTTTCCACTAAAAAATACAAAAAATTAACTGGGCGTGGTGGCGCATGCCTGTAAACCCAG ACCATGTTTCCACTAAAAAATACAAAAAATT_____GGCGTGGTGGCGCATGCCTGTAAACCCAG CCAGTT C OSGEP Ensembl:ENSG00000092094 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1004618509 Functional Loss DEL dbSNP153 32..36 33 - - - RMVar_hsa_circ_77874,RMVar_hsa_circ_165112 46467 RMVar_ID_46467 Human_SNP_ID_547171530 A-to-I Human chr14 - 20453829 20453829 20453829 TTTTTAGTAGAGTCGGGGTTTCCACCAGGCCAAGCTGGTCTCGAACTCCTGACCTCAGATGATCC TTTTTAGTAGAGTCGGGGTTTCCACCAGGCCAGGCTGGTCTCGAACTCCTGACCTCAGATGATCC T C OSGEP Ensembl:ENSG00000092094 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs992448925 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77874,RMVar_hsa_circ_165112 46468 RMVar_ID_46468 Human_SNP_ID_547171531 A-to-I Human chr14 - 20453829 20453829 20453829 TTTTTAGTAGAGTCGGGGTTTCCACCAGGCCAAGCTGGTCTCGAACTCCTGACCTCAGATGATCC TTTTTAGTAGAGTCGGGGTTTCCACCAGGCCACGCTGGTCTCGAACTCCTGACCTCAGATGATCC T G OSGEP Ensembl:ENSG00000092094 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs992448925 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77874,RMVar_hsa_circ_165112 46469 RMVar_ID_46469 Human_SNP_ID_547171536 A-to-I Human chr14 - 20453856 20453856 20453856 CGCCACCACATCCAGCTAAATTTTGTATTTTTAGTAGAGTCGGGGTTTCCACCAGGCCAAGCTGG CGCCACCACATCCAGCTAAATTTTGTATTTTTCGTAGAGTCGGGGTTTCCACCAGGCCAAGCTGG T G OSGEP Ensembl:ENSG00000092094 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1395625852 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6330294 RMVar_hsa_circ_77874,RMVar_hsa_circ_165112 46470 RMVar_ID_46470 Human_SNP_ID_547171547 A-to-I Human chr14 - 20453897 20453897 20453897 CTTCTACCCCAGCCTCCCAAGTAGCTAGGACTATAGGTGTGCGCCACCACATCCAGCTAAATTTT CTTCTACCCCAGCCTCCCAAGTAGCTAGGACTGTAGGTGTGCGCCACCACATCCAGCTAAATTTT T C OSGEP Ensembl:ENSG00000092094 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1019372472 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77874,RMVar_hsa_circ_165112 46471 RMVar_ID_46471 Human_SNP_ID_547171565 A-to-I Human chr14 - 20453972 20453972 20453972 CTCTGTCGCCCAGGCTGGAATGCAGTGGCACGATCTCGGCTCACTGCAATCTCTGCCTTCCAGGT CTCTGTCGCCCAGGCTGGAATGCAGTGGCACGGTCTCGGCTCACTGCAATCTCTGCCTTCCAGGT T C OSGEP Ensembl:ENSG00000092094 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1179696286 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77874,RMVar_hsa_circ_165112 46472 RMVar_ID_46472 Human_SNP_ID_547179053 A-to-I Human chr14 + 20480502 20480502 20480502 TACTTGGGAGGCTGAGGTGGGAGGATTGCTTGAGTCGGGGAGGCTGAGCCTTCAGTGAGCCATGA TACTTGGGAGGCTGAGGTGGGAGGATTGCTTGCGTCGGGGAGGCTGAGCCTTCAGTGAGCCATGA A C lnc-BBS5-6 RNACentral:URS0000E2127A lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1329192167 Functional Loss SNV dbSNP153 33..33 33 - - - 46473 RMVar_ID_46473 Human_SNP_ID_547179169 A-to-I Human chr14 + 20480981 20480981 20480981 GAGACCTTGTTTCTACAAAAAATTTAAAAATTAGCTGGGCATGGTGGTGCACACCTGTAGTCCCA GAGACCTTGTTTCTACAAAAAATTTAAAAATTTGCTGGGCATGGTGGTGCACACCTGTAGTCCCA A T lnc-BBS5-6 RNACentral:URS0000E2127A lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1193644610 Functional Loss SNV dbSNP153 33..33 33 - - - 46474 RMVar_ID_46474 Human_SNP_ID_547361237 A-to-I Human chr14 - 21162684 21162684 21162684 GCTTATCTGATGGTTTTGGTGGTTTTGGAATCATAATACCAGAGGATGCCATGACCCGGCTGTTG GCTTATCTGATGGTTTTGGTGGTTTTGGAATCGTAATACCAGAGGATGCCATGACCCGGCTGTTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1248868050 Functional Loss SNV dbSNP153 33..33 33 - - - 46475 RMVar_ID_46475 Human_SNP_ID_547370390 A-to-I Human chr14 - 21196950 21196950 21196950 ACTGTTTCTTCTACCACTCTTTTTACTGGAGTACAGTGGCATGATCTCGGCTCACTGCAATCTTC ACTGTTTCTTCTACCACTCTTTTTACTGGAGTGCAGTGGCATGATCTCGGCTCACTGCAATCTTC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1296231054 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16996304 46476 RMVar_ID_46476 Human_SNP_ID_547376587 A-to-I Human chr14 - 21218166 21218166 21218166 TGAGGTCCAGGAGCTCATGACCAGCCTGGCTAACATGGTGAAATCCCATCTCTACTAAAATTACA TGAGGTCCAGGAGCTCATGACCAGCCTGGCTAGCATGGTGAAATCCCATCTCTACTAAAATTACA T C HNRNPC Ensembl:ENSG00000092199 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1420774450 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17562307 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_51171,RMVar_hsa_circ_357744,RMVar_hsa_circ_346398,RMVar_hsa_circ_165141,RMVar_hsa_circ_67730 46477 RMVar_ID_46477 Human_SNP_ID_547376685 A-to-I Human chr14 - 21218464 21218464 21218464 CAGGCTAGTCTCTTAACTCATGATCTCAGGCAATCCACCTGCCTCGGCCTCCGGAAGTGCTGGGA CAGGCTAGTCTCTTAACTCATGATCTCAGGCAGTCCACCTGCCTCGGCCTCCGGAAGTGCTGGGA T C HNRNPC Ensembl:ENSG00000092199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1268204802 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12292301,Human_RBP_ID_17562311 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_51171,RMVar_hsa_circ_357744,RMVar_hsa_circ_346398,RMVar_hsa_circ_165141,RMVar_hsa_circ_67730 46478 RMVar_ID_46478 Human_SNP_ID_547376887 A-to-I Human chr14 - 21218925 21218925 21218925 TTGTATTTTTAGTAGAGATGGGGTTTCATCATATTAGCCAGGCTATTCTTGAACTCCTGATCTCA TTGTATTTTTAGTAGAGATGGGGTTTCATCATGTTAGCCAGGCTATTCTTGAACTCCTGATCTCA T C HNRNPC Ensembl:ENSG00000092199 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1202898526 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12292329 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_51171,RMVar_hsa_circ_357744,RMVar_hsa_circ_346398,RMVar_hsa_circ_165141,RMVar_hsa_circ_67730 46479 RMVar_ID_46479 Human_SNP_ID_547376898 A-to-I Human chr14 - 21218962 21218962 21218962 GGGACTACAAGCATGTGCCACCATGCCCAGCTAATATTTGTATTTTTAGTAGAGATGGGGTTTCA GGGACTACAAGCATGTGCCACCATGCCCAGCTCATATTTGTATTTTTAGTAGAGATGGGGTTTCA T G HNRNPC Ensembl:ENSG00000092199 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1316272448 Functional Loss SNV dbSNP153 33..33 33 - - - 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_51171,RMVar_hsa_circ_357744,RMVar_hsa_circ_346398,RMVar_hsa_circ_165141,RMVar_hsa_circ_67730 46480 RMVar_ID_46480 Human_SNP_ID_547377401 A-to-I Human chr14 - 21220392 21220392 21220392 AAATCCCATTTCTACCAAAAATACAAAAAATTAGCTGGGCGTGGTGGTGGGCGCCTGTAGTACAA AAATCCCATTTCTACCAAAAATACAAAAAATTTGCTGGGCGTGGTGGTGGGCGCCTGTAGTACAA T A HNRNPC Ensembl:ENSG00000092199 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs575226986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12292429 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_51171,RMVar_hsa_circ_357744,RMVar_hsa_circ_346398,RMVar_hsa_circ_165141,RMVar_hsa_circ_67730 46481 RMVar_ID_46481 Human_SNP_ID_547377408 A-to-I Human chr14 - 21220402 21220402 21220402 TAACATGGTGAAATCCCATTTCTACCAAAAATACAAAAAATTAGCTGGGCGTGGTGGTGGGCGCC TAACATGGTGAAATCCCATTTCTACCAAAAATGCAAAAAATTAGCTGGGCGTGGTGGTGGGCGCC T C HNRNPC Ensembl:ENSG00000092199 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1330878013 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12292429,Human_RBP_ID_25087321 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_51171,RMVar_hsa_circ_357744,RMVar_hsa_circ_346398,RMVar_hsa_circ_165141,RMVar_hsa_circ_67730 46482 RMVar_ID_46482 Human_SNP_ID_547380110 A-to-I Human chr14 - 21228902 21228902 21228902 TTTTGTATTTTTAGTAGAGGCTGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGAACT TTTTGTATTTTTAGTAGAGGCTGGGTTTCACCGTGTTGGCCAGGCTGGTCTCGAACTCCTGAACT T C HNRNPC Ensembl:ENSG00000092199 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs190959566 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_130 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_51171,RMVar_hsa_circ_357744,RMVar_hsa_circ_346398,RMVar_hsa_circ_165141,RMVar_hsa_circ_67730 46483 RMVar_ID_46483 Human_SNP_ID_547380111 A-to-I Human chr14 - 21228902 21228902 21228902 TTTTGTATTTTTAGTAGAGGCTGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCCTGAACT TTTTGTATTTTTAGTAGAGGCTGGGTTTCACCCTGTTGGCCAGGCTGGTCTCGAACTCCTGAACT T G HNRNPC Ensembl:ENSG00000092199 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs190959566 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_130 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_51171,RMVar_hsa_circ_357744,RMVar_hsa_circ_346398,RMVar_hsa_circ_165141,RMVar_hsa_circ_67730 46484 RMVar_ID_46484 Human_SNP_ID_547380134 A-to-I Human chr14 - 21228998 21228998 21228998 TCACTGCAACATACGCCTCTTTGGTTGAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGG TCACTGCAACATACGCCTCTTTGGTTGAAGCAGTTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGG T C HNRNPC Ensembl:ENSG00000092199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1457159160 Functional Loss SNV dbSNP153 33..33 33 - - - 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_51171,RMVar_hsa_circ_357744,RMVar_hsa_circ_346398,RMVar_hsa_circ_165141,RMVar_hsa_circ_67730 46485 RMVar_ID_46485 Human_SNP_ID_547381321 A-to-I Human chr14 - 21232888 21232888 21232888 GTACTACAGGCATGTGCCACCACACCTGGCTAATTTTTGTATTTTTTAGTAGAGGTGAGGTTTCA GTACTACAGGCATGTGCCACCACACCTGGCTATTTTTTGTATTTTTTAGTAGAGGTGAGGTTTCA T A HNRNPC Ensembl:ENSG00000092199 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1366497754 Functional Loss SNV dbSNP153 33..33 33 - - - 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 46486 RMVar_ID_46486 Human_SNP_ID_547381354 A-to-I Human chr14 - 21232975 21232975 21232975 TTGTGTGCAGTAGTGCAGTCTTGGCTAATTGTAACCTCAGCCTCCCGGGTTCAAGCGATTGTCCT TTGTGTGCAGTAGTGCAGTCTTGGCTAATTGTCACCTCAGCCTCCCGGGTTCAAGCGATTGTCCT T G HNRNPC Ensembl:ENSG00000092199 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1429318630 Functional Loss SNV dbSNP153 33..33 33 - - - 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 46487 RMVar_ID_46487 Human_SNP_ID_547381363 A-to-I Human chr14 - 21233035 21233029 21233036 AGACAATATATTCAGTCCTTTTTTTTTTTTTGAGACAGAGTCTAGCTCTGTTGTCCAGGATTGTG AGACAATATATTCAGTCCTTTTTTTTTTTTT_______AGTCTAGCTCTGTTGTCCAGGATTGTG TCTGTCTC T HNRNPC Ensembl:ENSG00000092199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1430206050 Functional Loss DEL dbSNP153 32..38 33 - - - Human_RBP_ID_6331151,Human_RBP_ID_12293158 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 46488 RMVar_ID_46488 Human_SNP_ID_547381365 A-to-I Human chr14 - 21233035 21233035 21233035 AGACAATATATTCAGTCCTTTTTTTTTTTTTGAGACAGAGTCTAGCTCTGTTGTCCAGGATTGTG AGACAATATATTCAGTCCTTTTTTTTTTTTTGTGACAGAGTCTAGCTCTGTTGTCCAGGATTGTG T A HNRNPC Ensembl:ENSG00000092199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1190838713 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6331151,Human_RBP_ID_12293158 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 46489 RMVar_ID_46489 Human_SNP_ID_547383281 A-to-I Human chr14 - 21239639 21239639 21239639 GAACTCCTGTCCTCAGGTGATTTGCTCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG GAACTCCTGTCCTCAGGTGATTTGCTCGCCTCCGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG T G HNRNPC Ensembl:ENSG00000092199 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs971700353 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12293541 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 46490 RMVar_ID_46490 Human_SNP_ID_547383664 A-to-I Human chr14 - 21241097 21241097 21241097 TGCCACCACCAATTTTTGTCTTTAGTAGAGACAGGGTTTCACCACGTTGGCCAGGCTGGTTTTGA TGCCACCACCAATTTTTGTCTTTAGTAGAGACTGGGTTTCACCACGTTGGCCAGGCTGGTTTTGA T A HNRNPC Ensembl:ENSG00000092199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388793793 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12293637 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 46491 RMVar_ID_46491 Human_SNP_ID_547383669 A-to-I Human chr14 - 21241106 21241106 21241106 ACAGACGCCTGCCACCACCAATTTTTGTCTTTAGTAGAGACAGGGTTTCACCACGTTGGCCAGGC ACAGACGCCTGCCACCACCAATTTTTGTCTTTTGTAGAGACAGGGTTTCACCACGTTGGCCAGGC T A HNRNPC Ensembl:ENSG00000092199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1221085167 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12293637 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 46492 RMVar_ID_46492 Human_SNP_ID_547384046 A-to-I Human chr14 - 21242317 21242317 21242317 ATCACGCCCAGCTAATTTTTAGTATTTTTTGTAGAGATGGGGTTTCACTATGTTGACCAGTTTGG ATCACGCCCAGCTAATTTTTAGTATTTTTTGTGGAGATGGGGTTTCACTATGTTGACCAGTTTGG T C HNRNPC Ensembl:ENSG00000092199 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1021016071 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12293738 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 46493 RMVar_ID_46493 Human_SNP_ID_547384050 A-to-I Human chr14 - 21242329 21242329 21242329 TAGGCGCTTGACATCACGCCCAGCTAATTTTTAGTATTTTTTGTAGAGATGGGGTTTCACTATGT TAGGCGCTTGACATCACGCCCAGCTAATTTTTGGTATTTTTTGTAGAGATGGGGTTTCACTATGT T C HNRNPC Ensembl:ENSG00000092199 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs181982085 Functional Loss SNV dbSNP153 33..33 33 - - - 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 46494 RMVar_ID_46494 Human_SNP_ID_547384247 A-to-I Human chr14 - 21242959 21242957 21242960 CACCACACCCAGCTTATCTTTGTATTGTTAGTAGAGATGGGGTTTCACCACATTGGCCATGCCGG CACCACACCCAGCTTATCTTTGTATTGTTAG___AGATGGGGTTTCACCACATTGGCCATGCCGG TCTA T HNRNPC Ensembl:ENSG00000092199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1292675713 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_12293786 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 46495 RMVar_ID_46495 Human_SNP_ID_547384666 A-to-I Human chr14 - 21244201 21244201 21244201 TGAGGTCAGGAGTTGGAGACCAGCTATGGTCAACATGGTGAAACCCCATCTCTACTAAAAGTACA TGAGGTCAGGAGTTGGAGACCAGCTATGGTCATCATGGTGAAACCCCATCTCTACTAAAAGTACA T A HNRNPC Ensembl:ENSG00000092199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1018803197 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9759468,Human_RBP_ID_12293891 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 46496 RMVar_ID_46496 Human_SNP_ID_547384926 A-to-I Human chr14 - 21244900 21244900 21244900 TTGTTATTTTAGTAGAGACTGGGTTTCACCATATTGGTCTGGTTGGTCTCAAACTCCGTGTTGGG TTGTTATTTTAGTAGAGACTGGGTTTCACCATGTTGGTCTGGTTGGTCTCAAACTCCGTGTTGGG T C HNRNPC Ensembl:ENSG00000092199 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs931301094 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1171438,Human_RBP_ID_4286753,Human_RBP_ID_5493344,Human_RBP_ID_12293930,Human_RBP_ID_23160597 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 46497 RMVar_ID_46497 Human_SNP_ID_547385320 A-to-I Human chr14 - 21245942 21245942 21245942 ACTCAGGAGGCTGAGGTGGCAAAATCGCTTGAACCTGGGAGGTGGAGGTTGTAGTGAACTGAGAC ACTCAGGAGGCTGAGGTGGCAAAATCGCTTGACCCTGGGAGGTGGAGGTTGTAGTGAACTGAGAC T G HNRNPC Ensembl:ENSG00000092199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1029077187 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12293993,Human_RBP_ID_25087693 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 46498 RMVar_ID_46498 Human_SNP_ID_547385325 A-to-I Human chr14 - 21245970 21245970 21245970 GTGGTGGTGCACATCTGTGTTCCCAGCTACTCAGGAGGCTGAGGTGGCAAAATCGCTTGAACCTG GTGGTGGTGCACATCTGTGTTCCCAGCTACTCGGGAGGCTGAGGTGGCAAAATCGCTTGAACCTG T C HNRNPC Ensembl:ENSG00000092199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984794955 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4286756,Human_RBP_ID_12293994 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 46499 RMVar_ID_46499 Human_SNP_ID_547385329 A-to-I Human chr14 - 21245990 21245990 21245990 GTCAAACCCCGTAGTCAGGCGTGGTGGTGCACATCTGTGTTCCCAGCTACTCAGGAGGCTGAGGT GTCAAACCCCGTAGTCAGGCGTGGTGGTGCACGTCTGTGTTCCCAGCTACTCAGGAGGCTGAGGT T C HNRNPC Ensembl:ENSG00000092199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1342716133 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12460481 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 46500 RMVar_ID_46500 Human_SNP_ID_547385350 A-to-I Human chr14 - 21246047 21246047 21246047 GGCCGAGGCAAGCAGATCCCCTCAGGTCAGGAATTTGAGAGCAGCCTGGCCAACATGGTCAAACC GGCCGAGGCAAGCAGATCCCCTCAGGTCAGGAGTTTGAGAGCAGCCTGGCCAACATGGTCAAACC T C HNRNPC Ensembl:ENSG00000092199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1272586785 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12293995 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 46501 RMVar_ID_46501 Human_SNP_ID_547385501 A-to-I Human chr14 - 21246509 21246509 21246509 AGGCTGGAGTGCAGTGGCGCAATCTCCAGCTCACTGCAAGCTCTGCCTCCCGGGTTCACGCCATT AGGCTGGAGTGCAGTGGCGCAATCTCCAGCTCGCTGCAAGCTCTGCCTCCCGGGTTCACGCCATT T C HNRNPC Ensembl:ENSG00000092199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs549722821 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12294020,Human_RBP_ID_25087712 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 46502 RMVar_ID_46502 Human_SNP_ID_547385505 A-to-I Human chr14 - 21246520 21246520 21246520 CTCTGTCTCCCAGGCTGGAGTGCAGTGGCGCAATCTCCAGCTCACTGCAAGCTCTGCCTCCCGGG CTCTGTCTCCCAGGCTGGAGTGCAGTGGCGCAGTCTCCAGCTCACTGCAAGCTCTGCCTCCCGGG T C HNRNPC Ensembl:ENSG00000092199 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1052393670 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12294020 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 46503 RMVar_ID_46503 Human_SNP_ID_547385897 A-to-I Human chr14 - 21247757 21247757 21247757 TTAGTAGAGATGGGGTTTCACCATGTTAGTCAAGCTGGTCTTGAACTCCTGTCCTCAAGTGTTCC TTAGTAGAGATGGGGTTTCACCATGTTAGTCAGGCTGGTCTTGAACTCCTGTCCTCAAGTGTTCC T C HNRNPC Ensembl:ENSG00000092199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1361825597 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6331431,Human_RBP_ID_12294101 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 46504 RMVar_ID_46504 Human_SNP_ID_547386040 A-to-I Human chr14 - 21248121 21248121 21248121 TTGGCCAGTCTGGTCTCTTAACTCCTGGGCTCAAGCAATCTCCCACCTCAGCCTCCAAAAGTTTT TTGGCCAGTCTGGTCTCTTAACTCCTGGGCTCGAGCAATCTCCCACCTCAGCCTCCAAAAGTTTT T C HNRNPC Ensembl:ENSG00000092199 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,frontal_cortex - 29129909,30559470 RNA-Seq:(High) rs955468215 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8250096,Human_RBP_ID_12294128,Human_RBP_ID_22922061 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 46505 RMVar_ID_46505 Human_SNP_ID_547387494 A-to-I Human chr14 - 21252422 21252422 21252422 TGTGTAATCCCAGCTACTTGGAAGTCTGAGGCAGAAGGATCCCTTGAACTCAGGAGGCAGAGGTT TGTGTAATCCCAGCTACTTGGAAGTCTGAGGCCGAAGGATCCCTTGAACTCAGGAGGCAGAGGTT T G HNRNPC Ensembl:ENSG00000092199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1390574422 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12294425,Human_RBP_ID_17562321 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 46506 RMVar_ID_46506 Human_SNP_ID_547387990 A-to-I Human chr14 - 21253876 21253876 21253876 TTTTTTTGGTAGAGACGGGGATTCACCGTGTTAGCCAGGATGGTGTCGATTTGCTGACCTCGTGA TTTTTTTGGTAGAGACGGGGATTCACCGTGTTGGCCAGGATGGTGTCGATTTGCTGACCTCGTGA T C HNRNPC Ensembl:ENSG00000092199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559628723 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6331596,Human_RBP_ID_12294498,Human_RBP_ID_23160635 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 46507 RMVar_ID_46507 Human_SNP_ID_547388362 A-to-I Human chr14 - 21254883 21254883 21254883 GAGTCTCGCTCTGTTGCCCAGGCTGGAGTGCAATGGCACGATCTTGGCTCACCGCAACCTCCGCC GAGTCTCGCTCTGTTGCCCAGGCTGGAGTGCAGTGGCACGATCTTGGCTCACCGCAACCTCCGCC T C HNRNPC Ensembl:ENSG00000092199 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1455098238 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2432299,Human_RBP_ID_12294582,Human_RBP_ID_25087906 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 46508 RMVar_ID_46508 Human_SNP_ID_547388800 A-to-I Human chr14 - 21256203 21256203 21256203 GACCTTGTGATCTGCCCGTCTCTGCCTCCCCAAAGTGCTGGGATTACAGGCGTGATCCACCACGC GACCTTGTGATCTGCCCGTCTCTGCCTCCCCAGAGTGCTGGGATTACAGGCGTGATCCACCACGC T C HNRNPC Ensembl:ENSG00000092199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006827674 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8401462,Human_RBP_ID_12294692 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 46509 RMVar_ID_46509 Human_SNP_ID_547388887 A-to-I Human chr14 - 21256448 21256448 21256448 GTATTGTTTGAAGGATTTTTTTTTTGGGGGGGAGATGGAGTTTTGCTCTCTTTGCCCAGGCTGTA GTATTGTTTGAAGGATTTTTTTTTTGGGGGGGGGATGGAGTTTTGCTCTCTTTGCCCAGGCTGTA T C HNRNPC Ensembl:ENSG00000092199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1321400731 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6331671,Human_RBP_ID_12294707 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 46510 RMVar_ID_46510 Human_SNP_ID_547389284 A-to-I Human chr14 - 21257691 21257691 21257691 AGTGTAGCTCCCTGGGAGGCTGAGGCGGTAGAATTAATTGAGTTCAGGAGTTTGAGGTCAGTGTG AGTGTAGCTCCCTGGGAGGCTGAGGCGGTAGATTTAATTGAGTTCAGGAGTTTGAGGTCAGTGTG T A HNRNPC Ensembl:ENSG00000092199 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs907962546 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6331711,Human_RBP_ID_9783493,Human_RBP_ID_12294829,Human_RBP_ID_22926795,Human_RBP_ID_25087972 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 46511 RMVar_ID_46511 Human_SNP_ID_547389302 A-to-I Human chr14 - 21257770 21257769 21257771 GATAGCTTAAGGCCAGGAAAGTCTGGCAACATAGCAAGAGCCTGTCTACAAAAAGCTGGGCACGG GATAGCTTAAGGCCAGGAAAGTCTGGCAACA__GCAAGAGCCTGTCTACAAAAAGCTGGGCACGG CTA C HNRNPC Ensembl:ENSG00000092199 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1261775670 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_9759698,Human_RBP_ID_12294839 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 46512 RMVar_ID_46512 Human_SNP_ID_547390420 A-to-I Human chr14 - 21261091 21261091 21261091 TGGTACCTGCCTGTAAGCCTGTAGTCACAACTAATTGGAAGGCTGAGGCAGGAGGGTCCCTTGGC TGGTACCTGCCTGTAAGCCTGTAGTCACAACTTATTGGAAGGCTGAGGCAGGAGGGTCCCTTGGC T A HNRNPC Ensembl:ENSG00000092199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1306077898 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12295030 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 46513 RMVar_ID_46513 Human_SNP_ID_547391779 A-to-I Human chr14 - 21266208 21266208 21266208 GTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCTGGGAGGTGGAGGTTGCAGTG GTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAGTCGCTTGAACCTGGGAGGTGGAGGTTGCAGTG T C HNRNPC Ensembl:ENSG00000092199 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs984644810 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_29581 46514 RMVar_ID_46514 Human_SNP_ID_547391829 A-to-I Human chr14 - 21266372 21266372 21266372 TTCTAAGGCCGGGTGTGGCTGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGTGG TTCTAAGGCCGGGTGTGGCTGCTCATGCCTGTGATCCCAGCACTTTGGGAGGCTGAGGCGGGTGG T C HNRNPC Ensembl:ENSG00000092199 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1387152567 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12295459 RMVar_hsa_circ_29581 46515 RMVar_ID_46515 Human_SNP_ID_547392540 A-to-I Human chr14 - 21268464 21268464 21268464 TAGTTAATGGAATACCTAGTTAATATAGTTCTAAAACTACTGTATTGCAATCTTTGCCAAGAACC TAGTTAATGGAATACCTAGTTAATATAGTTCTGAAACTACTGTATTGCAATCTTTGCCAAGAACC T C HNRNPC Ensembl:ENSG00000092199 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs756606514 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1816409,Human_RBP_ID_2408901,Human_RBP_ID_6332092,Human_RBP_ID_9759921,Human_RBP_ID_12295617,Human_RBP_ID_22922204,Human_RBP_ID_25088316 RMVar_hsa_circ_29581 46516 RMVar_ID_46516 Human_SNP_ID_547416516 A-to-I Human chr14 - 21354684 21354684 21354684 GGGAGGCTGAGGCAGGAGAATCACTTGAACCTAGGAGGCAGAGGTTGCAGTGAGCGAAGATTGTG GGGAGGCTGAGGCAGGAGAATCACTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCGAAGATTGTG T C SUPT16H Ensembl:ENSG00000092201 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1299873488 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81663,RMVar_hsa_circ_165152,RMVar_hsa_circ_80881,RMVar_hsa_circ_165153,RMVar_hsa_circ_165154,RMVar_hsa_circ_16434,RMVar_hsa_circ_100814,RMVar_hsa_circ_111065,RMVar_hsa_circ_165155 46517 RMVar_ID_46517 Human_SNP_ID_547422469 A-to-I Human chr14 - 21377057 21377057 21377057 TTTTTTTTTTTTTCTTTTTCTTTCTTTGAGACAGTCTCACTGTCGCCCAGGCTGGAGTGCAGTGA TTTTTTTTTTTTTCTTTTTCTTTCTTTGAGACGGTCTCACTGTCGCCCAGGCTGGAGTGCAGTGA T C SUPT16H Ensembl:ENSG00000092201 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1400071709 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12296010 RMVar_hsa_circ_88784,RMVar_hsa_circ_165160 46518 RMVar_ID_46518 Human_SNP_ID_547432347 A-to-I Human chr14 - 21411909 21411909 21411909 CAAGCGTGTGCCATCATGCCCGGCTAGTTTTTAAATTTCTAGTACAGACAGGGTTTCACCATGTT CAAGCGTGTGCCATCATGCCCGGCTAGTTTTTCAATTTCTAGTACAGACAGGGTTTCACCATGTT T G CHD8 Ensembl:ENSG00000100888 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1175290620 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114514,RMVar_hsa_circ_120022,RMVar_hsa_circ_112099,RMVar_hsa_circ_165173,RMVar_hsa_circ_84264,RMVar_hsa_circ_165174,RMVar_hsa_circ_165171,RMVar_hsa_circ_165172,RMVar_hsa_circ_165189,RMVar_hsa_circ_357510,RMVar_hsa_circ_369851,RMVar_hsa_circ_55742,RMVar_hsa_circ_165191,RMVar_hsa_circ_327295,RMVar_hsa_circ_38491,RMVar_hsa_circ_165198,RMVar_hsa_circ_63534,RMVar_hsa_circ_268654,RMVar_hsa_circ_320559,RMVar_hsa_circ_339663,RMVar_hsa_circ_72968,RMVar_hsa_circ_165197,RMVar_hsa_circ_165199,RMVar_hsa_circ_358635,RMVar_hsa_circ_58078,RMVar_hsa_circ_106429,RMVar_hsa_circ_165200 46519 RMVar_ID_46519 Human_SNP_ID_547432365 A-to-I Human chr14 - 21411988 21411988 21411988 GTGATCTTGGCTCATTGCAACCTCCGCCTCCCAGATTCAAGTAATTCTCATGCCTCAGCCTCCTG GTGATCTTGGCTCATTGCAACCTCCGCCTCCCGGATTCAAGTAATTCTCATGCCTCAGCCTCCTG T C CHD8 Ensembl:ENSG00000100888 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs532207165 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114514,RMVar_hsa_circ_120022,RMVar_hsa_circ_112099,RMVar_hsa_circ_165173,RMVar_hsa_circ_84264,RMVar_hsa_circ_165174,RMVar_hsa_circ_165171,RMVar_hsa_circ_165172,RMVar_hsa_circ_165189,RMVar_hsa_circ_357510,RMVar_hsa_circ_369851,RMVar_hsa_circ_55742,RMVar_hsa_circ_165191,RMVar_hsa_circ_327295,RMVar_hsa_circ_38491,RMVar_hsa_circ_165198,RMVar_hsa_circ_63534,RMVar_hsa_circ_268654,RMVar_hsa_circ_320559,RMVar_hsa_circ_339663,RMVar_hsa_circ_72968,RMVar_hsa_circ_165197,RMVar_hsa_circ_165199,RMVar_hsa_circ_358635,RMVar_hsa_circ_58078,RMVar_hsa_circ_106429,RMVar_hsa_circ_165200 46520 RMVar_ID_46520 Human_SNP_ID_547432443 A-to-I Human chr14 - 21412286 21412286 21412286 CAAAAATTAGCCAGGTGTGGTGGCACGTGCCTATAGTCCCAGCTACTCGGGAGGCTGAGGCAGGA CAAAAATTAGCCAGGTGTGGTGGCACGTGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGA T C CHD8 Ensembl:ENSG00000100888 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1037975809 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114514,RMVar_hsa_circ_120022,RMVar_hsa_circ_112099,RMVar_hsa_circ_165173,RMVar_hsa_circ_84264,RMVar_hsa_circ_165174,RMVar_hsa_circ_165171,RMVar_hsa_circ_165172,RMVar_hsa_circ_165189,RMVar_hsa_circ_357510,RMVar_hsa_circ_369851,RMVar_hsa_circ_55742,RMVar_hsa_circ_165191,RMVar_hsa_circ_327295,RMVar_hsa_circ_38491,RMVar_hsa_circ_165198,RMVar_hsa_circ_63534,RMVar_hsa_circ_268654,RMVar_hsa_circ_320559,RMVar_hsa_circ_339663,RMVar_hsa_circ_72968,RMVar_hsa_circ_165197,RMVar_hsa_circ_165199,RMVar_hsa_circ_358635,RMVar_hsa_circ_58078,RMVar_hsa_circ_106429,RMVar_hsa_circ_165200 46521 RMVar_ID_46521 Human_SNP_ID_547432460 A-to-I Human chr14 - 21412345 21412345 21412345 GGTTGGGAGTTTGAGACCAGCTTGGCCAACATAGTGAAACCCCGTCTCTACTAAAAATACAAAAA GGTTGGGAGTTTGAGACCAGCTTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAA T C CHD8 Ensembl:ENSG00000100888 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1235152385 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114514,RMVar_hsa_circ_120022,RMVar_hsa_circ_112099,RMVar_hsa_circ_165173,RMVar_hsa_circ_84264,RMVar_hsa_circ_165174,RMVar_hsa_circ_165171,RMVar_hsa_circ_165172,RMVar_hsa_circ_165189,RMVar_hsa_circ_357510,RMVar_hsa_circ_369851,RMVar_hsa_circ_55742,RMVar_hsa_circ_165191,RMVar_hsa_circ_327295,RMVar_hsa_circ_38491,RMVar_hsa_circ_165198,RMVar_hsa_circ_63534,RMVar_hsa_circ_268654,RMVar_hsa_circ_320559,RMVar_hsa_circ_339663,RMVar_hsa_circ_72968,RMVar_hsa_circ_165197,RMVar_hsa_circ_165199,RMVar_hsa_circ_358635,RMVar_hsa_circ_58078,RMVar_hsa_circ_106429,RMVar_hsa_circ_165200 46522 RMVar_ID_46522 Human_SNP_ID_547435250 A-to-I Human chr14 - 21423179 21423179 21423179 AGAGTCTGCTCTGTTGCCCAAGCTGGAGTGCAATGGCGCAATCTTGGCTCACTGCAACCTCTGCC AGAGTCTGCTCTGTTGCCCAAGCTGGAGTGCAGTGGCGCAATCTTGGCTCACTGCAACCTCTGCC T C CHD8 Ensembl:ENSG00000100888 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs918316747 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114514,RMVar_hsa_circ_112099,RMVar_hsa_circ_165171,RMVar_hsa_circ_165172,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_165202 46523 RMVar_ID_46523 Human_SNP_ID_547441305 A-to-I Human chr14 - 21445606 21445606 21445606 TGCCTCACTGCAGCCTCTGCCTACTGGATTCAAGCAATTCTCCTGCCTCAGCCTCCCAGGTAGCT TGCCTCACTGCAGCCTCTGCCTACTGGATTCAGGCAATTCTCCTGCCTCAGCCTCCCAGGTAGCT T C CHD8 Ensembl:ENSG00000100888 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1190020467 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12297081 46524 RMVar_ID_46524 Human_SNP_ID_547442946 A-to-I Human chr14 - 21452152 21452152 21452152 CCTGTAGGCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCAGGGAGGCGGAGATG CCTGTAGGCCCAGCTACTCGGGAGGCTGAGGCGGGAGAATCACTTGAACCAGGGAGGCGGAGATG T C CHD8 Ensembl:ENSG00000100888 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054190754 Functional Loss SNV dbSNP153 33..33 33 - - - 46525 RMVar_ID_46525 Human_SNP_ID_547443650 A-to-I Human chr14 - 21454446 21454446 21454446 GGGCATGGTGACGCGTGCCTGTAGTCCCAGCTACATGGGAGGCCAAGGCATGAAAATCGCTTGAA GGGCATGGTGACGCGTGCCTGTAGTCCCAGCTGCATGGGAGGCCAAGGCATGAAAATCGCTTGAA T C CHD8 Ensembl:ENSG00000100888 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1468561641 Functional Loss SNV dbSNP153 33..33 33 - - - 46526 RMVar_ID_46526 Human_SNP_ID_547443651 A-to-I Human chr14 - 21454446 21454446 21454446 GGGCATGGTGACGCGTGCCTGTAGTCCCAGCTACATGGGAGGCCAAGGCATGAAAATCGCTTGAA GGGCATGGTGACGCGTGCCTGTAGTCCCAGCTCCATGGGAGGCCAAGGCATGAAAATCGCTTGAA T G CHD8 Ensembl:ENSG00000100888 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1468561641 Functional Loss SNV dbSNP153 33..33 33 - - - 46527 RMVar_ID_46527 Human_SNP_ID_547445453 A-to-I Human chr14 - 21460463 21460463 21460463 CTCCTGCCTCAACCTCCCGAGTAGCTGGGACTACAGGCATGTGCCACCACACCTGGCTCATTTTT CTCCTGCCTCAACCTCCCGAGTAGCTGGGACTTCAGGCATGTGCCACCACACCTGGCTCATTTTT T A RAB2B Ensembl:ENSG00000129472 Protein coding 3'UTR GSE38233;GSE100210;GSE99789;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,29796672,32596459 RNA-Seq:(High) rs1022909668 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 46528 RMVar_ID_46528 Human_SNP_ID_547445454 A-to-I Human chr14 - 21460473 21460473 21460473 TCAAGCAGTTCTCCTGCCTCAACCTCCCGAGTAGCTGGGACTACAGGCATGTGCCACCACACCTG TCAAGCAGTTCTCCTGCCTCAACCTCCCGAGTGGCTGGGACTACAGGCATGTGCCACCACACCTG T C RAB2B Ensembl:ENSG00000129472 Protein coding 3'UTR GSE38233;GSE100210;GSE99789;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,29796672,32596459 RNA-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 46529 RMVar_ID_46529 Human_SNP_ID_547445466 A-to-I Human chr14 - 21460502 21460502 21460502 TGGCTCACTGCAACCTCCACTTTCCAGGTTCAAGCAGTTCTCCTGCCTCAACCTCCCGAGTAGCT TGGCTCACTGCAACCTCCACTTTCCAGGTTCACGCAGTTCTCCTGCCTCAACCTCCCGAGTAGCT T G RAB2B Ensembl:ENSG00000129472 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388408916 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 46530 RMVar_ID_46530 Human_SNP_ID_547445468 A-to-I Human chr14 - 21460509 21460509 21460509 ATGATCTTGGCTCACTGCAACCTCCACTTTCCAGGTTCAAGCAGTTCTCCTGCCTCAACCTCCCG ATGATCTTGGCTCACTGCAACCTCCACTTTCCGGGTTCAAGCAGTTCTCCTGCCTCAACCTCCCG T C RAB2B Ensembl:ENSG00000129472 Protein coding 3'UTR GSE107867;GSE123020:GSM3490832,GSM3490833,GSM3490834 ASD brains,Fragile X samples from UC Davis FXTAS brain repository;esophageal squamous carcinoma cells,KYSE180 cell line - 30559470,32596459 RNA-Seq:(High) rs564541203 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 46531 RMVar_ID_46531 Human_SNP_ID_547445472 A-to-I Human chr14 - 21460522 21460522 21460522 GGAGTGCAGTGGCATGATCTTGGCTCACTGCAACCTCCACTTTCCAGGTTCAAGCAGTTCTCCTG GGAGTGCAGTGGCATGATCTTGGCTCACTGCAGCCTCCACTTTCCAGGTTCAAGCAGTTCTCCTG T C RAB2B Ensembl:ENSG00000129472 Protein coding 3'UTR GSE38233;GSE100210;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,temporal_cortex - 24183664,29129909,30559470 RNA-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 46532 RMVar_ID_46532 Human_SNP_ID_547445565 A-to-I Human chr14 - 21460681 21460681 21460681 TGAACCCAGGAGGTGAAGGTTACGCTAAGCCAAGATCACGCCATTGCACTGCAGCCTGGGCAACA TGAACCCAGGAGGTGAAGGTTACGCTAAGCCAGGATCACGCCATTGCACTGCAGCCTGGGCAACA T C RAB2B Ensembl:ENSG00000129472 Protein coding 3'UTR GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs532455287 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6406591,Human_RBP_ID_22472903 RMVar_hsa_circ_105125,RMVar_hsa_circ_120911,RMVar_hsa_circ_165206,RMVar_hsa_circ_82966,RMVar_hsa_circ_165207,RMVar_hsa_circ_165205 46533 RMVar_ID_46533 Human_SNP_ID_547445591 A-to-I Human chr14 - 21460751 21460743 21460751 AAATTAGCTGGGTGTGGTGGTGCATGCCTGTAATCCCAGGTACTCGGGAGGCCAAGGCAGGAGAA AAATTAGCTGGGTGTGGTGGTGCATGCCTGTA________TACTCGGGAGGCCAAGGCAGGAGAA ACCTGGGAT A RAB2B Ensembl:ENSG00000129472 Protein coding 3'UTR GSE99789;GSE123020:GSM3490829,GSM3490830,GSM3490831 esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109 cell line - 29796672,32596459 RNA-Seq:(High) rs1281180612 Functional Loss DEL dbSNP153 33..40 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 46534 RMVar_ID_46534 Human_SNP_ID_547445602 A-to-I Human chr14 - 21460786 21460786 21460786 CAACTTGGAGAAATGCCATCTCAACTGAAAATACAAAATTAGCTGGGTGTGGTGGTGCATGCCTG CAACTTGGAGAAATGCCATCTCAACTGAAAATGCAAAATTAGCTGGGTGTGGTGGTGCATGCCTG T C RAB2B Ensembl:ENSG00000129472 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs928709910 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18647782 RMVar_hsa_circ_105125,RMVar_hsa_circ_120911,RMVar_hsa_circ_165206,RMVar_hsa_circ_82966,RMVar_hsa_circ_165207,RMVar_hsa_circ_165205 46535 RMVar_ID_46535 Human_SNP_ID_547445603 A-to-I Human chr14 - 21460789 21460789 21460789 GACCAACTTGGAGAAATGCCATCTCAACTGAAAATACAAAATTAGCTGGGTGTGGTGGTGCATGC GACCAACTTGGAGAAATGCCATCTCAACTGAAGATACAAAATTAGCTGGGTGTGGTGGTGCATGC T C RAB2B Ensembl:ENSG00000129472 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs775681203 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18647782 RMVar_hsa_circ_105125,RMVar_hsa_circ_120911,RMVar_hsa_circ_165206,RMVar_hsa_circ_82966,RMVar_hsa_circ_165207,RMVar_hsa_circ_165205 46536 RMVar_ID_46536 Human_SNP_ID_547445605 A-to-I Human chr14 - 21460801 21460801 21460801 CGAGACCAGCCTGACCAACTTGGAGAAATGCCATCTCAACTGAAAATACAAAATTAGCTGGGTGT CGAGACCAGCCTGACCAACTTGGAGAAATGCCGTCTCAACTGAAAATACAAAATTAGCTGGGTGT T C RAB2B Ensembl:ENSG00000129472 Protein coding 3'UTR GSE38233;GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,32596459 RNA-Seq:(High) rs566161348 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18647782 RMVar_hsa_circ_105125,RMVar_hsa_circ_120911,RMVar_hsa_circ_165206,RMVar_hsa_circ_82966,RMVar_hsa_circ_165207,RMVar_hsa_circ_165205 46537 RMVar_ID_46537 Human_SNP_ID_547445606 A-to-I Human chr14 - 21460801 21460801 21460801 CGAGACCAGCCTGACCAACTTGGAGAAATGCCATCTCAACTGAAAATACAAAATTAGCTGGGTGT CGAGACCAGCCTGACCAACTTGGAGAAATGCCCTCTCAACTGAAAATACAAAATTAGCTGGGTGT T G RAB2B Ensembl:ENSG00000129472 Protein coding 3'UTR GSE38233;GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,32596459 RNA-Seq:(High) rs566161348 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18647782 RMVar_hsa_circ_105125,RMVar_hsa_circ_120911,RMVar_hsa_circ_165206,RMVar_hsa_circ_82966,RMVar_hsa_circ_165207,RMVar_hsa_circ_165205 46538 RMVar_ID_46538 Human_SNP_ID_547445628 A-to-I Human chr14 - 21460901 21460901 21460901 GTAGTTAAAAAATAATTTCATGGCGGGGCGCCATGGCTCATGCCTGTAATCCTAGCACTTTGGGA GTAGTTAAAAAATAATTTCATGGCGGGGCGCCGTGGCTCATGCCTGTAATCCTAGCACTTTGGGA T C RAB2B Ensembl:ENSG00000129472 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1429126708 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 46539 RMVar_ID_46539 Human_SNP_ID_547448324 A-to-I Human chr14 - 21471496 21471496 21471496 CTCCCACCTCAGCCCCTCAAGTAGCTGGGACTACAGATGTGTGCCATCACACCTGGCTAATTTTT CTCCCACCTCAGCCCCTCAAGTAGCTGGGACTGCAGATGTGTGCCATCACACCTGGCTAATTTTT T C RAB2B Ensembl:ENSG00000129472 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1274210146 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105125,RMVar_hsa_circ_165205 46540 RMVar_ID_46540 Human_SNP_ID_547455488 A-to-I Human chr14 + 21497661 21497661 21497661 GCGATTCTCCTGCATCAGCCTCCCGAGTAGCTAGGATTACAGGCGCCCGCCACTACGCCCAGCTA GCGATTCTCCTGCATCAGCCTCCCGAGTAGCTGGGATTACAGGCGCCCGCCACTACGCCCAGCTA A G TOX4 Ensembl:ENSG00000092203 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs921618076 Functional Loss SNV dbSNP153 33..33 33 - - - 46541 RMVar_ID_46541 Human_SNP_ID_547455576 A-to-I Human chr14 + 21497897 21497897 21497897 TAGAGATGGGGTCTCACTATGTTGCCCAGTCTAGTCTTGAACTCCTGGGCTACAGTTACCCTCCT TAGAGATGGGGTCTCACTATGTTGCCCAGTCTGGTCTTGAACTCCTGGGCTACAGTTACCCTCCT A G TOX4 Ensembl:ENSG00000092203 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054372911 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4287456,Human_RBP_ID_6406606,Human_RBP_ID_12297726 46542 RMVar_ID_46542 Human_SNP_ID_547741314 A-to-I Human chr14 - 22569308 22569308 22569308 CTGCCTCAGCCTCTTGAGTAGCTGGGACTACAAGTGTGTGCTCCCACGCCTGGCTAATTTTTGTA CTGCCTCAGCCTCTTGAGTAGCTGGGACTACAGGTGTGTGCTCCCACGCCTGGCTAATTTTTGTA T C DAD1 Ensembl:ENSG00000129562 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs774878394 Functional Loss SNV dbSNP153 33..33 33 - - - 46543 RMVar_ID_46543 Human_SNP_ID_547741317 A-to-I Human chr14 - 22569333 22569333 22569333 CGCCTCCTGGGTTTAAGCAGTTCTCCTGCCTCAGCCTCTTGAGTAGCTGGGACTACAAGTGTGTG CGCCTCCTGGGTTTAAGCAGTTCTCCTGCCTCGGCCTCTTGAGTAGCTGGGACTACAAGTGTGTG T C DAD1 Ensembl:ENSG00000129562 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11628014 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23615960 GWAS_ID_5735,GWAS_ID_5736 46544 RMVar_ID_46544 Human_SNP_ID_547741330 A-to-I Human chr14 - 22569407 22569407 22569407 TTTTTTTGAGACGGAGTCTCGCTTTGTTGTCCAGGCTGTAGTGCAGTGGCATGATCTTGGCTCAC TTTTTTTGAGACGGAGTCTCGCTTTGTTGTCCGGGCTGTAGTGCAGTGGCATGATCTTGGCTCAC T C DAD1 Ensembl:ENSG00000129562 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1291432663 Functional Loss SNV dbSNP153 33..33 33 - - - 46545 RMVar_ID_46545 Human_SNP_ID_547741783 A-to-I Human chr14 - 22571156 22571156 22571156 GCACTTGCCCGGCTAGTTTTTGTATTTTTAGTAGAGATGGGGTTTCACTCTGTTGGCTAGGCTGG GCACTTGCCCGGCTAGTTTTTGTATTTTTAGTGGAGATGGGGTTTCACTCTGTTGGCTAGGCTGG T C DAD1 Ensembl:ENSG00000129562 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1272642279 Functional Loss SNV dbSNP153 33..33 33 - - - 46546 RMVar_ID_46546 Human_SNP_ID_547742052 A-to-I Human chr14 - 22571812 22571810 22571812 CAGCCTGGCCAACATGGTGAAACCTCGTCTCTACTAAAAAGACAAAAATTAGCTGGGCGTGGTGG CAGCCTGGCCAACATGGTGAAACCTCGTCTCT__TAAAAAGACAAAAATTAGCTGGGCGTGGTGG AGT A DAD1 Ensembl:ENSG00000129562 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1292404692 Functional Loss DEL dbSNP153 33..34 33 - - - 46547 RMVar_ID_46547 Human_SNP_ID_547742409 A-to-I Human chr14 - 22573287 22573287 22573287 ATATTGTTGGCTGGGCGTGGTGGTTCATGCCTATAATCCCAGCACTTTCGGAAGGCGAGGTGGGC ATATTGTTGGCTGGGCGTGGTGGTTCATGCCTGTAATCCCAGCACTTTCGGAAGGCGAGGTGGGC T C DAD1 Ensembl:ENSG00000129562 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs773044903 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17562334 RMVar_hsa_circ_165218 46548 RMVar_ID_46548 Human_SNP_ID_547742923 A-to-I Human chr14 - 22575173 22575173 22575173 GAACAAAGCGGATTTCCAAGGCATCTCCCCAGAGCGAGCCTTTGCTGATTTTCTCTTTGCCAGCA GAACAAAGCGGATTTCCAAGGCATCTCCCCAGGGCGAGCCTTTGCTGATTTTCTCTTTGCCAGCA T C DAD1 Ensembl:ENSG00000129562 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs961142234 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22438634,Human_RBP_ID_22757820,Human_RBP_ID_22797509 Human_Splice_Rec_1492704,Human_Splice_Rec_1492708,Human_Splice_Rec_1492714 Human_miRNA_ID_934773,Human_miRNA_ID_2424782,Human_miRNA_ID_2434444,Human_miRNA_ID_2882798 RMVar_hsa_circ_311225,RMVar_hsa_circ_165218,RMVar_hsa_circ_165219 46549 RMVar_ID_46549 Human_SNP_ID_547811463 A-to-I Human chr14 + 22831926 22831926 22831926 ATACTCGGGAGGCTGAGGCAGGAGAATCGCTTAAGCCCAGGAGGCAGAGGTTGTAATAATCTGAG ATACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAGCCCAGGAGGCAGAGGTTGTAATAATCTGAG A G MRPL52 Ensembl:ENSG00000172590 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1423749801 Functional Loss SNV dbSNP153 33..33 33 - - - 46550 RMVar_ID_46550 Human_SNP_ID_547811578 A-to-I Human chr14 + 22832470 22832470 22832470 TCAGGCCATTCTCATGCCTCAGCCTCCCTAGTAGTTGAGACTACAGGCGCCCACCACCACGCCCG TCAGGCCATTCTCATGCCTCAGCCTCCCTAGTGGTTGAGACTACAGGCGCCCACCACCACGCCCG A G MRPL52 Ensembl:ENSG00000172590 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1233575273 Functional Loss SNV dbSNP153 33..33 33 - - - 46551 RMVar_ID_46551 Human_SNP_ID_547811650 A-to-I Human chr14 + 22832758 22832758 22832758 TAAATTAGCCGGGTGTGGTGGTGCGCACCTGTAATCCCAGTTACTCGGGAGGCTGAGGCAGGAGA TAAATTAGCCGGGTGTGGTGGTGCGCACCTGTGATCCCAGTTACTCGGGAGGCTGAGGCAGGAGA A G MRPL52 Ensembl:ENSG00000172590 Protein coding intron GSE38233;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,32596459 RNA-Seq:(High) rs1480890698 Functional Loss SNV dbSNP153 33..33 33 - - - 46552 RMVar_ID_46552 Human_SNP_ID_547811711 A-to-I Human chr14 + 22833013 22833013 22833013 TATCCTGGCCAACTTGGTGAAATCCCGTCTCTACTAAAAATACAAAAATTAGCCAGGGATGGTGG TATCCTGGCCAACTTGGTGAAATCCCGTCTCTCCTAAAAATACAAAAATTAGCCAGGGATGGTGG A C MRPL52 Ensembl:ENSG00000172590 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1368813404 Functional Loss SNV dbSNP153 33..33 33 - - - 46553 RMVar_ID_46553 Human_SNP_ID_547811712 A-to-I Human chr14 + 22833013 22833013 22833013 TATCCTGGCCAACTTGGTGAAATCCCGTCTCTACTAAAAATACAAAAATTAGCCAGGGATGGTGG TATCCTGGCCAACTTGGTGAAATCCCGTCTCTGCTAAAAATACAAAAATTAGCCAGGGATGGTGG A G MRPL52 Ensembl:ENSG00000172590 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1368813404 Functional Loss SNV dbSNP153 33..33 33 - - - 46554 RMVar_ID_46554 Human_SNP_ID_547811727 A-to-I Human chr14 + 22833063 22833063 22833063 AGCCAGGGATGGTGGCACGTGTTTGTAGTCCCAGCTACTCGGGAGTCTGAGGCAGGATAATCTCT AGCCAGGGATGGTGGCACGTGTTTGTAGTCCCCGCTACTCGGGAGTCTGAGGCAGGATAATCTCT A C MRPL52 Ensembl:ENSG00000172590 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs138731228 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22711633 46555 RMVar_ID_46555 Human_SNP_ID_547811936 A-to-I Human chr14 + 22833810 22833810 22833810 CACCCAGCTAACTTTGTATTTTTAGTAGAGACAGGGTTTTTCTATGTTGGTCAGACTGGTCTTGA CACCCAGCTAACTTTGTATTTTTAGTAGAGACTGGGTTTTTCTATGTTGGTCAGACTGGTCTTGA A T MRPL52 Ensembl:ENSG00000172590 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs542749684 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12299088 46556 RMVar_ID_46556 Human_SNP_ID_547812171 A-to-I Human chr14 + 22834727 22834727 22834727 ACAATTAGCCGGGCGTGGTGGGGTGCGCTTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA ACAATTAGCCGGGCGTGGTGGGGTGCGCTTGTGATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA A G MRPL52 Ensembl:ENSG00000172590 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1399687193 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12299117 46557 RMVar_ID_46557 Human_SNP_ID_547824565 A-to-I Human chr14 + 22880500 22880500 22880500 GAGGGGCCAAGGCAGGCGGATCGCTTGAGGCCAAGAGTTCAAGAACAGCCTGGGCAACATGATGA GAGGGGCCAAGGCAGGCGGATCGCTTGAGGCCCAGAGTTCAAGAACAGCCTGGGCAACATGATGA A C LRP10 Ensembl:ENSG00000197324 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs981023737 Functional Loss SNV dbSNP153 33..33 33 - - - 46558 RMVar_ID_46558 Human_SNP_ID_547824566 A-to-I Human chr14 + 22880500 22880500 22880500 GAGGGGCCAAGGCAGGCGGATCGCTTGAGGCCAAGAGTTCAAGAACAGCCTGGGCAACATGATGA GAGGGGCCAAGGCAGGCGGATCGCTTGAGGCCGAGAGTTCAAGAACAGCCTGGGCAACATGATGA A G LRP10 Ensembl:ENSG00000197324 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs981023737 Functional Loss SNV dbSNP153 33..33 33 - - - 46559 RMVar_ID_46559 Human_SNP_ID_547832251 A-to-I Human chr14 - 22908137 22908137 22908137 ACATGTTTGTACTCCCAGCTACTTGGGAGGCTAAGGCTGGAGGATTGCTTGGGCCCAGGAGTTCG ACATGTTTGTACTCCCAGCTACTTGGGAGGCTGAGGCTGGAGGATTGCTTGGGCCCAGGAGTTCG T C RBM23 Ensembl:ENSG00000100461 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1395227903 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12299299 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 46560 RMVar_ID_46560 Human_SNP_ID_547832408 A-to-I Human chr14 - 22908570 22908570 22908570 GGCCAACATAGCGAAACCTTGTCTCTACTAAAAATATAAAAAATTAGCTGGGCATGATGGTACAT GGCCAACATAGCGAAACCTTGTCTCTACTAAACATATAAAAAATTAGCTGGGCATGATGGTACAT T G RBM23 Ensembl:ENSG00000100461 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1413389215 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_292108,RMVar_hsa_circ_165250,RMVar_hsa_circ_272527,RMVar_hsa_circ_165253,RMVar_hsa_circ_165251,RMVar_hsa_circ_325563 46561 RMVar_ID_46561 Human_SNP_ID_547833768 A-to-I Human chr14 - 22912917 22912917 22912917 TGGCTAACTGCAACCTCCGCCTCCTGGGTTCAAGTGATACTCCTGCCTCAGCCTCCCGAGTAGCT TGGCTAACTGCAACCTCCGCCTCCTGGGTTCAGGTGATACTCCTGCCTCAGCCTCCCGAGTAGCT T C RBM23 Ensembl:ENSG00000100461 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs187125660 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86214,RMVar_hsa_circ_165242,RMVar_hsa_circ_165251,RMVar_hsa_circ_165257 46562 RMVar_ID_46562 Human_SNP_ID_547833893 A-to-I Human chr14 - 22913158 22913158 22913158 CGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAAGCATGAGCCACCGCGCCCGGCCTTCTTGT CGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTGCAAGCATGAGCCACCGCGCCCGGCCTTCTTGT T C RBM23 Ensembl:ENSG00000100461 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1021898185 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86214,RMVar_hsa_circ_165242,RMVar_hsa_circ_165251,RMVar_hsa_circ_165257 46563 RMVar_ID_46563 Human_SNP_ID_547834069 A-to-I Human chr14 - 22913663 22913663 22913663 TTGTATTTTTAGTAGAGATGAGGTTTCACCATATTGGCCAGGCTGGTCTCAAACTCCTGACCTCA TTGTATTTTTAGTAGAGATGAGGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTCCTGACCTCA T C RBM23 Ensembl:ENSG00000100461 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1157699566 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25089369 RMVar_hsa_circ_86214,RMVar_hsa_circ_165242,RMVar_hsa_circ_165251,RMVar_hsa_circ_165257 46564 RMVar_ID_46564 Human_SNP_ID_547834192 A-to-I Human chr14 - 22914083 22914083 22914083 TGACCTTATGATCAAACTGCCTCGGCCTTCCAAAGTGCTGGGATTACAGGTGTGAGCCACCATGC TGACCTTATGATCAAACTGCCTCGGCCTTCCAGAGTGCTGGGATTACAGGTGTGAGCCACCATGC T C RBM23 Ensembl:ENSG00000100461 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1434905857 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86214,RMVar_hsa_circ_165242 46565 RMVar_ID_46565 Human_SNP_ID_547834193 A-to-I Human chr14 - 22914083 22914083 22914083 TGACCTTATGATCAAACTGCCTCGGCCTTCCAAAGTGCTGGGATTACAGGTGTGAGCCACCATGC TGACCTTATGATCAAACTGCCTCGGCCTTCCACAGTGCTGGGATTACAGGTGTGAGCCACCATGC T G RBM23 Ensembl:ENSG00000100461 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1434905857 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86214,RMVar_hsa_circ_165242 46566 RMVar_ID_46566 Human_SNP_ID_547834423 A-to-I Human chr14 - 22914783 22914783 22914783 GGATGAGGTTTCACCATATCCGTCAGGCTGGTATTGAACTCCTGACCTCAGGTGATCCACCCACC GGATGAGGTTTCACCATATCCGTCAGGCTGGTGTTGAACTCCTGACCTCAGGTGATCCACCCACC T C RBM23 Ensembl:ENSG00000100461 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1286131833 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86214,RMVar_hsa_circ_165242 46567 RMVar_ID_46567 Human_SNP_ID_547834426 A-to-I Human chr14 - 22914798 22914798 22914798 TTGTGTCTTTAATGGGGATGAGGTTTCACCATATCCGTCAGGCTGGTATTGAACTCCTGACCTCA TTGTGTCTTTAATGGGGATGAGGTTTCACCATGTCCGTCAGGCTGGTATTGAACTCCTGACCTCA T C RBM23 Ensembl:ENSG00000100461 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1222144304 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23160704 RMVar_hsa_circ_86214,RMVar_hsa_circ_165242 46568 RMVar_ID_46568 Human_SNP_ID_547834431 A-to-I Human chr14 - 22914820 22914820 22914820 CACCACCATGCCCGGCTAATTTTTGTGTCTTTAATGGGGATGAGGTTTCACCATATCCGTCAGGC CACCACCATGCCCGGCTAATTTTTGTGTCTTTGATGGGGATGAGGTTTCACCATATCCGTCAGGC T C RBM23 Ensembl:ENSG00000100461 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1283164624 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86214,RMVar_hsa_circ_165242 46569 RMVar_ID_46569 Human_SNP_ID_547834450 A-to-I Human chr14 - 22914883 22914883 22914883 TGCCTCCCAGGTTCAAGCGATTCTCCTGTCTTAGCCTCTTGAGTAGCTGGGACTACAGGCGCCCA TGCCTCCCAGGTTCAAGCGATTCTCCTGTCTTTGCCTCTTGAGTAGCTGGGACTACAGGCGCCCA T A RBM23 Ensembl:ENSG00000100461 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1198531552 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86214,RMVar_hsa_circ_165242 46570 RMVar_ID_46570 Human_SNP_ID_547834805 A-to-I Human chr14 - 22916001 22916001 22916001 GTATTGCCCAGGCTGATTTTGACTTGGCCTCAAGCCATTCTCCAGCCTTAGCTTCCCAAAGTGCT GTATTGCCCAGGCTGATTTTGACTTGGCCTCAGGCCATTCTCCAGCCTTAGCTTCCCAAAGTGCT T C RBM23 Ensembl:ENSG00000100461 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs757627875 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86214,RMVar_hsa_circ_165242 46571 RMVar_ID_46571 Human_SNP_ID_547834856 A-to-I Human chr14 - 22916164 22916164 22916164 CTGCACAGACTGGATTGCAGCGGCATGATCACAGTTCACTGCAGCCTCAACTTCCTGGGTTCAAG CTGCACAGACTGGATTGCAGCGGCATGATCACGGTTCACTGCAGCCTCAACTTCCTGGGTTCAAG T C RBM23 Ensembl:ENSG00000100461 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1247783444 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86214,RMVar_hsa_circ_165242 46572 RMVar_ID_46572 Human_SNP_ID_547834999 A-to-I Human chr14 - 22916540 22916540 22916540 AATTAGCTCCTCTGGCCAGATGTAATCCTAGTACTTTGGGAGGCTAAGGTGGGTGGATCTGTTGA AATTAGCTCCTCTGGCCAGATGTAATCCTAGTGCTTTGGGAGGCTAAGGTGGGTGGATCTGTTGA T C RBM23 Ensembl:ENSG00000100461 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1024140235 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86214,RMVar_hsa_circ_165242 46573 RMVar_ID_46573 Human_SNP_ID_547835003 A-to-I Human chr14 - 22916548 22916548 22916548 TGATCAAGAATTAGCTCCTCTGGCCAGATGTAATCCTAGTACTTTGGGAGGCTAAGGTGGGTGGA TGATCAAGAATTAGCTCCTCTGGCCAGATGTACTCCTAGTACTTTGGGAGGCTAAGGTGGGTGGA T G RBM23 Ensembl:ENSG00000100461 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025765389 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12299476 RMVar_hsa_circ_86214,RMVar_hsa_circ_165242 46574 RMVar_ID_46574 Human_SNP_ID_547835149 A-to-I Human chr14 - 22916997 22916997 22916997 AGGTGTGGTGGTGCCTGCCTGTAATCCCAGCTACTTGGGAGACTGAGACAGGAGAATTGCTTGAA AGGTGTGGTGGTGCCTGCCTGTAATCCCAGCTGCTTGGGAGACTGAGACAGGAGAATTGCTTGAA T C RBM23 Ensembl:ENSG00000100461 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs183539565 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86214,RMVar_hsa_circ_165242 46575 RMVar_ID_46575 Human_SNP_ID_547837518 A-to-I Human chr14 - 22924903 22924902 22924903 AATGCCTATGAACTCTTTGCCAAGGGCTATGAAGACTATCTGCAGTCCCCGCTTCAGGTGGGTCT AATGCCTATGAACTCTTTGCCAAGGGCTATGA_GACTATCTGCAGTCCCCGCTTCAGGTGGGTCT CT C PRMT5 Ensembl:ENSG00000100462 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1283632472 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_881201,Human_RBP_ID_1491493,Human_RBP_ID_1816815,Human_RBP_ID_3444567,Human_RBP_ID_3944809,Human_RBP_ID_8401916,Human_RBP_ID_8793880,Human_RBP_ID_17478666,Human_RBP_ID_22438468,Human_RBP_ID_24367379 Human_Splice_Rec_1493775,Human_Splice_Rec_1493811,Human_Splice_Rec_1493843,Human_Splice_Rec_1493873,Human_Splice_Rec_1493921,Human_Splice_Rec_1493951,Human_Splice_Rec_1493971,Human_Splice_Rec_1493989,Human_Splice_Rec_1493997,Human_Splice_Rec_1494007,Human_Splice_Rec_1494015 RMVar_hsa_circ_91236,RMVar_hsa_circ_165260,RMVar_hsa_circ_89103,RMVar_hsa_circ_372379,RMVar_hsa_circ_9143,RMVar_hsa_circ_92953,RMVar_hsa_circ_165261,RMVar_hsa_circ_165262,RMVar_hsa_circ_109845,RMVar_hsa_circ_165263,RMVar_hsa_circ_371167,RMVar_hsa_circ_165264,RMVar_hsa_circ_165265 46576 RMVar_ID_46576 Human_SNP_ID_547841819 A-to-I Human chr14 - 22940383 22940383 22940383 TTATCTAAAGAGTAAGGTTGGCTGGGCGCTGTAGCTTATGCCTGTAATCCCAGCACTTTGGGAGG TTATCTAAAGAGTAAGGTTGGCTGGGCGCTGTGGCTTATGCCTGTAATCCCAGCACTTTGGGAGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270790075 Functional Loss SNV dbSNP153 33..33 33 - - - 46577 RMVar_ID_46577 Human_SNP_ID_547843604 A-to-I Human chr14 - 22946957 22946957 22946957 AATATGGTGAAACCCTGTCTCTACTAAAAAATACAAAAATTAGCTGGGCATGGTGGCATGTGCCT AATATGGTGAAACCCTGTCTCTACTAAAAAATGCAAAAATTAGCTGGGCATGGTGGCATGTGCCT T C AL132780.3,HAUS4 Ensembl:ENSG00000259132,Ensembl:ENSG00000092036 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1326379683 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107309,RMVar_hsa_circ_165271 46578 RMVar_ID_46578 Human_SNP_ID_547843605 A-to-I Human chr14 - 22946959 22946958 22946959 CCAATATGGTGAAACCCTGTCTCTACTAAAAAATACAAAAATTAGCTGGGCATGGTGGCATGTGC CCAATATGGTGAAACCCTGTCTCTACTAAAAA_TACAAAAATTAGCTGGGCATGGTGGCATGTGC AT A AL132780.3,HAUS4 Ensembl:ENSG00000259132,Ensembl:ENSG00000092036 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1316897216 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_107309,RMVar_hsa_circ_165271 46579 RMVar_ID_46579 Human_SNP_ID_547844184 A-to-I Human chr14 - 22948781 22948781 22948781 CCTGTAATACCATCACTTTGGGAGGCCGAGGCAGGTGGATCATGAGGTCAGGCGTTCGAGACCAA CCTGTAATACCATCACTTTGGGAGGCCGAGGCGGGTGGATCATGAGGTCAGGCGTTCGAGACCAA T C AL132780.3,HAUS4 Ensembl:ENSG00000259132,Ensembl:ENSG00000092036 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs925841316 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_165273,RMVar_hsa_circ_290636,RMVar_hsa_circ_334123,RMVar_hsa_circ_372284,RMVar_hsa_circ_346267,RMVar_hsa_circ_303918,RMVar_hsa_circ_165275,RMVar_hsa_circ_165274,RMVar_hsa_circ_61500,RMVar_hsa_circ_320450,RMVar_hsa_circ_165272,RMVar_hsa_circ_345922,RMVar_hsa_circ_267892,RMVar_hsa_circ_165277 46580 RMVar_ID_46580 Human_SNP_ID_547844458 A-to-I Human chr14 + 22949654 22949654 22949654 AATATGAATACTACGTCTAGAAACACATTATTATAAACAGCTTGACATAAATGGTATTATACCCT AATATGAATACTACGTCTAGAAACACATTATTGTAAACAGCTTGACATAAATGGTATTATACCCT A G AL132780.1 Ensembl:ENSG00000257285 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1357271914 Functional Loss SNV dbSNP153 33..33 33 - - - 46581 RMVar_ID_46581 Human_SNP_ID_547845170 A-to-I Human chr14 - 22952371 22952371 22952371 CAGAGTCATTCAAGAGTTGCTTGTGGACTACTATGTGAAGATACAAGACACAAATGTAACTTCTG CAGAGTCATTCAAGAGTTGCTTGTGGACTACTGTGTGAAGATACAAGACACAAATGTAACTTCTG T C AL132780.3,HAUS4 Ensembl:ENSG00000259132,Ensembl:ENSG00000092036 Protein coding,Protein coding intron,5'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs978427406 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_443571,Human_RBP_ID_1816827,Human_RBP_ID_9368418,Human_RBP_ID_17856574,Human_RBP_ID_18979208,Human_RBP_ID_23208491,Human_RBP_ID_23616186,Human_RBP_ID_26324564 Human_Splice_Rec_1494118,Human_Splice_Rec_1494119,Human_Splice_Rec_1494136,Human_Splice_Rec_1494137,Human_Splice_Rec_1494152,Human_Splice_Rec_1494153,Human_Splice_Rec_1494166,Human_Splice_Rec_1494167,Human_Splice_Rec_1494184,Human_Splice_Rec_1494185,Human_Splice_Rec_1494200,Human_Splice_Rec_1494201,Human_Splice_Rec_1494212,Human_Splice_Rec_1494213,Human_Splice_Rec_1494228,Human_Splice_Rec_1494229,Human_Splice_Rec_1494243,Human_Splice_Rec_1494260,Human_Splice_Rec_1494261,Human_Splice_Rec_1494274,Human_Splice_Rec_1494275,Human_Splice_Rec_1494284,Human_Splice_Rec_1494285,Human_Splice_Rec_1494298,Human_Splice_Rec_1494299,Human_Splice_Rec_1494310,Human_Splice_Rec_1494311,Human_Splice_Rec_1494322,Human_Splice_Rec_1494323,Human_Splice_Rec_1494334,Human_Splice_Rec_1494335,Human_Splice_Rec_1494340,Human_Splice_Rec_1494341,Human_Splice_Rec_1494346,Human_Splice_Rec_1494347 RMVar_hsa_circ_6608,RMVar_hsa_circ_165273,RMVar_hsa_circ_290636,RMVar_hsa_circ_334123,RMVar_hsa_circ_372284,RMVar_hsa_circ_165274,RMVar_hsa_circ_290879,RMVar_hsa_circ_320450,RMVar_hsa_circ_165272,RMVar_hsa_circ_345922,RMVar_hsa_circ_165277,RMVar_hsa_circ_324093,RMVar_hsa_circ_165278,RMVar_hsa_circ_286838,RMVar_hsa_circ_29595,RMVar_hsa_circ_65828,RMVar_hsa_circ_353459 46582 RMVar_ID_46582 Human_SNP_ID_547847668 A-to-I Human chr14 + 22962453 22962453 22962453 GGTGTCTCTCTGTCTCGCAGAGGTATGATCACAGCTCACTGCAGCCTTGACCTCCCAGGCTCGGG GGTGTCTCTCTGTCTCGCAGAGGTATGATCACGGCTCACTGCAGCCTTGACCTCCCAGGCTCGGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs981908610 Functional Loss SNV dbSNP153 33..33 33 - - - 46583 RMVar_ID_46583 Human_SNP_ID_547849486 A-to-I Human chr14 - 22969684 22969684 22969684 TTGCCCAGGCTGGTCTTGAATTTCTGGCCTCAAGTGATCTCCCACTTTGGCCTCCTAAGTCACTG TTGCCCAGGCTGGTCTTGAATTTCTGGCCTCAGGTGATCTCCCACTTTGGCCTCCTAAGTCACTG T C AL132780.3 Ensembl:ENSG00000259132 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs927643880 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17562783 46584 RMVar_ID_46584 Human_SNP_ID_547850111 A-to-I Human chr14 - 22972167 22972167 22972167 CTGATTTGATACTAGTCAGTTTGCTTGAAACTAGTTCACCTAAAGCTAGATCTCTTAAAACCAAT CTGATTTGATACTAGTCAGTTTGCTTGAAACTGGTTCACCTAAAGCTAGATCTCTTAAAACCAAT T C AL132780.3,AJUBA Ensembl:ENSG00000259132,Ensembl:ENSG00000129474 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048655 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27430513 46585 RMVar_ID_46585 Human_SNP_ID_547850112 A-to-I Human chr14 - 22972170 22972170 22972170 ACACTGATTTGATACTAGTCAGTTTGCTTGAAACTAGTTCACCTAAAGCTAGATCTCTTAAAACC ACACTGATTTGATACTAGTCAGTTTGCTTGAAGCTAGTTCACCTAAAGCTAGATCTCTTAAAACC T C AL132780.3,AJUBA Ensembl:ENSG00000259132,Ensembl:ENSG00000129474 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048654 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27430513 46586 RMVar_ID_46586 Human_SNP_ID_547850115 A-to-I Human chr14 - 22972186 22972186 22972186 AACTGGAGGGAGCAAAACACTGATTTGATACTAGTCAGTTTGCTTGAAACTAGTTCACCTAAAGC AACTGGAGGGAGCAAAACACTGATTTGATACTGGTCAGTTTGCTTGAAACTAGTTCACCTAAAGC T C AL132780.3,AJUBA Ensembl:ENSG00000259132,Ensembl:ENSG00000129474 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048652 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27430513 Human_miRNA_ID_932392,Human_miRNA_ID_1006039 46587 RMVar_ID_46587 Human_SNP_ID_547850116 A-to-I Human chr14 - 22972189 22972189 22972189 GGGAACTGGAGGGAGCAAAACACTGATTTGATACTAGTCAGTTTGCTTGAAACTAGTTCACCTAA GGGAACTGGAGGGAGCAAAACACTGATTTGATGCTAGTCAGTTTGCTTGAAACTAGTTCACCTAA T C AL132780.3,AJUBA Ensembl:ENSG00000259132,Ensembl:ENSG00000129474 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1465185316 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27430513 Human_miRNA_ID_932392 46588 RMVar_ID_46588 Human_SNP_ID_547850127 A-to-I Human chr14 - 22972233 22972233 22972233 GGGTCCCGGATTGCATCCATCACAATCCCAAAACTAGAGTTGGGGGGAACTGGAGGGAGCAAAAC GGGTCCCGGATTGCATCCATCACAATCCCAAAGCTAGAGTTGGGGGGAACTGGAGGGAGCAAAAC T C AL132780.3,AJUBA Ensembl:ENSG00000259132,Ensembl:ENSG00000129474 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348551178 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17846455,Human_RBP_ID_26431577 46589 RMVar_ID_46589 Human_SNP_ID_547850128 A-to-I Human chr14 - 22972234 22972234 22972234 GGGGTCCCGGATTGCATCCATCACAATCCCAAAACTAGAGTTGGGGGGAACTGGAGGGAGCAAAA GGGGTCCCGGATTGCATCCATCACAATCCCAAGACTAGAGTTGGGGGGAACTGGAGGGAGCAAAA T C AL132780.3,AJUBA Ensembl:ENSG00000259132,Ensembl:ENSG00000129474 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1291321064 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17846455,Human_RBP_ID_26431577 46590 RMVar_ID_46590 Human_SNP_ID_547850138 A-to-I Human chr14 - 22972267 22972265 22972267 TTCCTAGTAGAAGCTCACTTGCCACCTCTCAGAGGGGTCCCGGATTGCATCCATCACAATCCCAA TTCCTAGTAGAAGCTCACTTGCCACCTCTCAG__GGGTCCCGGATTGCATCCATCACAATCCCAA CCT C AL132780.3,AJUBA Ensembl:ENSG00000259132,Ensembl:ENSG00000129474 Protein coding,Protein coding intron,3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1334070925 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_231712,Human_RBP_ID_18207104,Human_RBP_ID_26428008,Human_RBP_ID_27430514 46591 RMVar_ID_46591 Human_SNP_ID_547850140 A-to-I Human chr14 - 22972267 22972267 22972267 TTCCTAGTAGAAGCTCACTTGCCACCTCTCAGAGGGGTCCCGGATTGCATCCATCACAATCCCAA TTCCTAGTAGAAGCTCACTTGCCACCTCTCAGGGGGGTCCCGGATTGCATCCATCACAATCCCAA T C AL132780.3,AJUBA Ensembl:ENSG00000259132,Ensembl:ENSG00000129474 Protein coding,Protein coding intron,3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1325593359 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_231712,Human_RBP_ID_18207104,Human_RBP_ID_26428008,Human_RBP_ID_27430514 46592 RMVar_ID_46592 Human_SNP_ID_547850259 A-to-I Human chr14 - 22972819 22972819 22972819 GGTTGATGCAGTGTGGGATGTCCCTGAGAGGTAGCAAGTCTAGGGTGGTGAGTTCCTGCTAGGCA GGTTGATGCAGTGTGGGATGTCCCTGAGAGGTGGCAAGTCTAGGGTGGTGAGTTCCTGCTAGGCA T C AL132780.3,AJUBA Ensembl:ENSG00000259132,Ensembl:ENSG00000129474 Protein coding,Protein coding intron,3'UTR GSE38233;GSE100210;GSE112787;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;293 Flip-In T-REx cells,empty vector;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,29967493,32596459 RNA-Seq:(High) rs551777758 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17687020,Human_RBP_ID_17846460,Human_RBP_ID_26431578,Human_RBP_ID_27430516 46593 RMVar_ID_46593 Human_SNP_ID_547850267 A-to-I Human chr14 - 22972842 22972842 22972842 AAACCCCAGAGTTTTGGGGTTGTGGTTGATGCAGTGTGGGATGTCCCTGAGAGGTAGCAAGTCTA AAACCCCAGAGTTTTGGGGTTGTGGTTGATGCGGTGTGGGATGTCCCTGAGAGGTAGCAAGTCTA T C AL132780.3,AJUBA Ensembl:ENSG00000259132,Ensembl:ENSG00000129474 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs11551973 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26431938,Human_RBP_ID_27430516 Human_miRNA_ID_619060 46594 RMVar_ID_46594 Human_SNP_ID_547850276 A-to-I Human chr14 - 22972901 22972901 22972901 TAGTTTCAGCTAAACTGACTAGAACCAAATCAAAGTGTAATTCTCCCTCCAGCTCCCCCAAACCC TAGTTTCAGCTAAACTGACTAGAACCAAATCACAGTGTAATTCTCCCTCCAGCTCCCCCAAACCC T G AL132780.3,AJUBA Ensembl:ENSG00000259132,Ensembl:ENSG00000129474 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1220435836 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23306743 Human_miRNA_ID_1364533 46595 RMVar_ID_46595 Human_SNP_ID_547850277 A-to-I Human chr14 - 22972905 22972905 22972905 CAATTAGTTTCAGCTAAACTGACTAGAACCAAATCAAAGTGTAATTCTCCCTCCAGCTCCCCCAA CAATTAGTTTCAGCTAAACTGACTAGAACCAATTCAAAGTGTAATTCTCCCTCCAGCTCCCCCAA T A AL132780.3,AJUBA Ensembl:ENSG00000259132,Ensembl:ENSG00000129474 Protein coding,Protein coding intron,3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs113406822 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23306743 Human_miRNA_ID_1364533 46596 RMVar_ID_46596 Human_SNP_ID_547850278 A-to-I Human chr14 - 22972905 22972905 22972905 CAATTAGTTTCAGCTAAACTGACTAGAACCAAATCAAAGTGTAATTCTCCCTCCAGCTCCCCCAA CAATTAGTTTCAGCTAAACTGACTAGAACCAAGTCAAAGTGTAATTCTCCCTCCAGCTCCCCCAA T C AL132780.3,AJUBA Ensembl:ENSG00000259132,Ensembl:ENSG00000129474 Protein coding,Protein coding intron,3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs113406822 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23306743 Human_miRNA_ID_1364533 46597 RMVar_ID_46597 Human_SNP_ID_547850279 A-to-I Human chr14 - 22972905 22972905 22972905 CAATTAGTTTCAGCTAAACTGACTAGAACCAAATCAAAGTGTAATTCTCCCTCCAGCTCCCCCAA CAATTAGTTTCAGCTAAACTGACTAGAACCAACTCAAAGTGTAATTCTCCCTCCAGCTCCCCCAA T G AL132780.3,AJUBA Ensembl:ENSG00000259132,Ensembl:ENSG00000129474 Protein coding,Protein coding intron,3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs113406822 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23306743 Human_miRNA_ID_1364533 46598 RMVar_ID_46598 Human_SNP_ID_547850280 A-to-I Human chr14 - 22972906 22972906 22972906 TCAATTAGTTTCAGCTAAACTGACTAGAACCAAATCAAAGTGTAATTCTCCCTCCAGCTCCCCCA TCAATTAGTTTCAGCTAAACTGACTAGAACCATATCAAAGTGTAATTCTCCCTCCAGCTCCCCCA T A AL132780.3,AJUBA Ensembl:ENSG00000259132,Ensembl:ENSG00000129474 Protein coding,Protein coding intron,3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs113656933 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23306743 Human_miRNA_ID_1364533 46599 RMVar_ID_46599 Human_SNP_ID_547850281 A-to-I Human chr14 - 22972906 22972906 22972906 TCAATTAGTTTCAGCTAAACTGACTAGAACCAAATCAAAGTGTAATTCTCCCTCCAGCTCCCCCA TCAATTAGTTTCAGCTAAACTGACTAGAACCAGATCAAAGTGTAATTCTCCCTCCAGCTCCCCCA T C AL132780.3,AJUBA Ensembl:ENSG00000259132,Ensembl:ENSG00000129474 Protein coding,Protein coding intron,3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs113656933 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23306743 Human_miRNA_ID_1364533 46600 RMVar_ID_46600 Human_SNP_ID_547850288 A-to-I Human chr14 - 22972939 22972939 22972939 CTGGATTCCAGGAGTAGAGGACCTAGCTTTAAATCAATTAGTTTCAGCTAAACTGACTAGAACCA CTGGATTCCAGGAGTAGAGGACCTAGCTTTAAGTCAATTAGTTTCAGCTAAACTGACTAGAACCA T C AL132780.3,AJUBA Ensembl:ENSG00000259132,Ensembl:ENSG00000129474 Protein coding,Protein coding intron,3'UTR GSE47997;GSE100210;GSE99789;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,29129909,29796672,32596459 RNA-Seq:(High) rs924315483 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17562789,Human_RBP_ID_27430517 46601 RMVar_ID_46601 Human_SNP_ID_547850289 A-to-I Human chr14 - 22972940 22972940 22972940 CCTGGATTCCAGGAGTAGAGGACCTAGCTTTAAATCAATTAGTTTCAGCTAAACTGACTAGAACC CCTGGATTCCAGGAGTAGAGGACCTAGCTTTAGATCAATTAGTTTCAGCTAAACTGACTAGAACC T C AL132780.3,AJUBA Ensembl:ENSG00000259132,Ensembl:ENSG00000129474 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs3210229 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17562789,Human_RBP_ID_27430517 46602 RMVar_ID_46602 Human_SNP_ID_547850311 A-to-I Human chr14 - 22973036 22973036 22973036 CTCCCACCTTGGCCTCCCAAAGTGCTGGGATTATAGGCGTAAGCCACTGTGTCTGGCCTAGTGTA CTCCCACCTTGGCCTCCCAAAGTGCTGGGATTGTAGGCGTAAGCCACTGTGTCTGGCCTAGTGTA T C AL132780.3,AJUBA Ensembl:ENSG00000259132,Ensembl:ENSG00000129474 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947901682 Functional Loss SNV dbSNP153 33..33 33 - - - 46603 RMVar_ID_46603 Human_SNP_ID_547850331 A-to-I Human chr14 - 22973110 22973110 22973110 TATTTTGTTTGTTTTAGAGATGGGATCTCACCATGTTGCCCAGGCTAGTCTTGAACTCCTGGGCT TATTTTGTTTGTTTTAGAGATGGGATCTCACCTTGTTGCCCAGGCTAGTCTTGAACTCCTGGGCT T A AL132780.3,AJUBA Ensembl:ENSG00000259132,Ensembl:ENSG00000129474 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1326221829 Functional Loss SNV dbSNP153 33..33 33 - - - 46604 RMVar_ID_46604 Human_SNP_ID_547864026 A-to-I Human chr14 - 23026578 23026578 23026578 GGGCGTGGTTACGAGCGCTTGTAATCCTAGCTACCTGGGAAACTGAGGCAGGAGAATCACTTTAA GGGCGTGGTTACGAGCGCTTGTAATCCTAGCTGCCTGGGAAACTGAGGCAGGAGAATCACTTTAA T C PSMB5 Ensembl:ENSG00000100804 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1240363893 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76086,RMVar_hsa_circ_92067,RMVar_hsa_circ_165286,RMVar_hsa_circ_165287 46605 RMVar_ID_46605 Human_SNP_ID_547864120 A-to-I Human chr14 - 23026880 23026880 23026880 TGGGGTTTCTTCATGTTGGTCAGGCTGGTCTCAAACGCCTGACCTCAGGTGATCTGCCCACCTCA TGGGGTTTCTTCATGTTGGTCAGGCTGGTCTCGAACGCCTGACCTCAGGTGATCTGCCCACCTCA T C PSMB5 Ensembl:ENSG00000100804 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1234197483 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76086,RMVar_hsa_circ_92067,RMVar_hsa_circ_165286,RMVar_hsa_circ_165287 46606 RMVar_ID_46606 Human_SNP_ID_547864799 A-to-I Human chr14 - 23029581 23029580 23029582 GATTGTGCCATTGCACTCCAGCTTGGGAAACAAGAAAGAAACTTTGTCTCAAAAATCAGTCAGTC GATTGTGCCATTGCACTCCAGCTTGGGAAAC__GAAAGAAACTTTGTCTCAAAAATCAGTCAGTC CTT C PSMB5 Ensembl:ENSG00000100804 Protein coding intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs909118162 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_76086,RMVar_hsa_circ_92067,RMVar_hsa_circ_165286,RMVar_hsa_circ_165287,RMVar_hsa_circ_165288,RMVar_hsa_circ_123321 46607 RMVar_ID_46607 Human_SNP_ID_547864805 A-to-I Human chr14 - 23029623 23029623 23029623 TCAATCACTTGAACCTGGGAGGCAGAGGTTGCAGTAAGCTGAGATTGTGCCATTGCACTCCAGCT TCAATCACTTGAACCTGGGAGGCAGAGGTTGCGGTAAGCTGAGATTGTGCCATTGCACTCCAGCT T C PSMB5 Ensembl:ENSG00000100804 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs952342913 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76086,RMVar_hsa_circ_92067,RMVar_hsa_circ_165286,RMVar_hsa_circ_165287,RMVar_hsa_circ_165288,RMVar_hsa_circ_123321 46608 RMVar_ID_46608 Human_SNP_ID_547864817 A-to-I Human chr14 - 23029679 23029679 23029679 AACCCTGGAGGTGCATGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCAATCACT AACCCTGGAGGTGCATGCCTGTAATCCCAGCTGCTCAGGAGGCTGAGGCAGGAGAATCAATCACT T C PSMB5 Ensembl:ENSG00000100804 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1449236863 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76086,RMVar_hsa_circ_92067,RMVar_hsa_circ_165286,RMVar_hsa_circ_165287,RMVar_hsa_circ_165288,RMVar_hsa_circ_123321 46609 RMVar_ID_46609 Human_SNP_ID_547864818 A-to-I Human chr14 - 23029689 23029689 23029689 GAATCTCTTGAACCCTGGAGGTGCATGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA GAATCTCTTGAACCCTGGAGGTGCATGCCTGTTATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA T A PSMB5 Ensembl:ENSG00000100804 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs549476700 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17562792 RMVar_hsa_circ_76086,RMVar_hsa_circ_92067,RMVar_hsa_circ_165286,RMVar_hsa_circ_165287,RMVar_hsa_circ_165288,RMVar_hsa_circ_123321 46610 RMVar_ID_46610 Human_SNP_ID_547864819 A-to-I Human chr14 - 23029689 23029689 23029689 GAATCTCTTGAACCCTGGAGGTGCATGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA GAATCTCTTGAACCCTGGAGGTGCATGCCTGTGATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA T C PSMB5 Ensembl:ENSG00000100804 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs549476700 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17562792 RMVar_hsa_circ_76086,RMVar_hsa_circ_92067,RMVar_hsa_circ_165286,RMVar_hsa_circ_165287,RMVar_hsa_circ_165288,RMVar_hsa_circ_123321 46611 RMVar_ID_46611 Human_SNP_ID_547864826 A-to-I Human chr14 - 23029732 23029732 23029732 GCACATGCCTGTAATCCCAGCTACTCAGGGAGATGAGGCAGGAGAATCTCTTGAACCCTGGAGGT GCACATGCCTGTAATCCCAGCTACTCAGGGAGCTGAGGCAGGAGAATCTCTTGAACCCTGGAGGT T G PSMB5 Ensembl:ENSG00000100804 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1289030075 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17562339 RMVar_hsa_circ_76086,RMVar_hsa_circ_92067,RMVar_hsa_circ_165286,RMVar_hsa_circ_165287,RMVar_hsa_circ_165288,RMVar_hsa_circ_123321 46612 RMVar_ID_46612 Human_SNP_ID_547865133 A-to-I Human chr14 - 23030842 23030842 23030842 CAGTTCATTGCAACCTCCACCTCCTGGGTTCAAGTGATCTCCTGCCTCAGCCTCCCGAGTAGCTG CAGTTCATTGCAACCTCCACCTCCTGGGTTCAGGTGATCTCCTGCCTCAGCCTCCCGAGTAGCTG T C PSMB5 Ensembl:ENSG00000100804 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1481300806 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76086,RMVar_hsa_circ_92067,RMVar_hsa_circ_165286,RMVar_hsa_circ_165287,RMVar_hsa_circ_165288,RMVar_hsa_circ_123321 46613 RMVar_ID_46613 Human_SNP_ID_547865384 A-to-I Human chr14 - 23031988 23031988 23031988 GCCTCCCAGGTTCAAGTGATTCTCCTGCCTCAACCTTCCATGTAGCTGAGACTACAGGCATATGC GCCTCCCAGGTTCAAGTGATTCTCCTGCCTCAGCCTTCCATGTAGCTGAGACTACAGGCATATGC T C PSMB5 Ensembl:ENSG00000100804 Protein coding intron GSE38233;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,32596459 RNA-Seq:(High) rs1351283845 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76086,RMVar_hsa_circ_92067,RMVar_hsa_circ_165286,RMVar_hsa_circ_165287,RMVar_hsa_circ_165288,RMVar_hsa_circ_123321 46614 RMVar_ID_46614 Human_SNP_ID_547865479 A-to-I Human chr14 - 23032290 23032290 23032290 ACAAGCGCCCACCAGCATGCCCAGCTAATTTTATATTTTTAGTAGAGATGGGGTTTCACCATGTT ACAAGCGCCCACCAGCATGCCCAGCTAATTTTTTATTTTTAGTAGAGATGGGGTTTCACCATGTT T A PSMB5 Ensembl:ENSG00000100804 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2331829 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76086,RMVar_hsa_circ_92067,RMVar_hsa_circ_165286,RMVar_hsa_circ_165287,RMVar_hsa_circ_165288,RMVar_hsa_circ_123321 46615 RMVar_ID_46615 Human_SNP_ID_547865480 A-to-I Human chr14 - 23032290 23032290 23032290 ACAAGCGCCCACCAGCATGCCCAGCTAATTTTATATTTTTAGTAGAGATGGGGTTTCACCATGTT ACAAGCGCCCACCAGCATGCCCAGCTAATTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTT T C PSMB5 Ensembl:ENSG00000100804 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2331829 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76086,RMVar_hsa_circ_92067,RMVar_hsa_circ_165286,RMVar_hsa_circ_165287,RMVar_hsa_circ_165288,RMVar_hsa_circ_123321 46616 RMVar_ID_46616 Human_SNP_ID_547865481 A-to-I Human chr14 - 23032290 23032290 23032290 ACAAGCGCCCACCAGCATGCCCAGCTAATTTTATATTTTTAGTAGAGATGGGGTTTCACCATGTT ACAAGCGCCCACCAGCATGCCCAGCTAATTTTCTATTTTTAGTAGAGATGGGGTTTCACCATGTT T G PSMB5 Ensembl:ENSG00000100804 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2331829 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76086,RMVar_hsa_circ_92067,RMVar_hsa_circ_165286,RMVar_hsa_circ_165287,RMVar_hsa_circ_165288,RMVar_hsa_circ_123321 46617 RMVar_ID_46617 Human_SNP_ID_547865506 A-to-I Human chr14 - 23032392 23032392 23032392 TCGTCCAGTCTGGCGTGTAATGGCATTGTTTCAGCTCACTACAACCTCTGCCTCCTGGGTTCAAG TCGTCCAGTCTGGCGTGTAATGGCATTGTTTCCGCTCACTACAACCTCTGCCTCCTGGGTTCAAG T G PSMB5 Ensembl:ENSG00000100804 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs988972355 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76086,RMVar_hsa_circ_92067,RMVar_hsa_circ_165286,RMVar_hsa_circ_165287,RMVar_hsa_circ_165288,RMVar_hsa_circ_123321 46618 RMVar_ID_46618 Human_SNP_ID_547865518 A-to-I Human chr14 - 23032431 23032431 23032431 TCTTTTTTTCTTTTTTTGAGATGCAAAGTTTCACTCCGATCGTCCAGTCTGGCGTGTAATGGCAT TCTTTTTTTCTTTTTTTGAGATGCAAAGTTTCCCTCCGATCGTCCAGTCTGGCGTGTAATGGCAT T G PSMB5 Ensembl:ENSG00000100804 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1279961365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12300016,Human_RBP_ID_19923011,Human_RBP_ID_23160716 RMVar_hsa_circ_76086,RMVar_hsa_circ_92067,RMVar_hsa_circ_165286,RMVar_hsa_circ_165287,RMVar_hsa_circ_165288,RMVar_hsa_circ_123321 46619 RMVar_ID_46619 Human_SNP_ID_547877999 A-to-I Human chr14 - 23074478 23074478 23074478 TCACTGCAACCTCCGCCTCCTGGGTTCAAGCAATTATCATGCCTCAGCCTCCTGAGTATCTGGGA TCACTGCAACCTCCGCCTCCTGGGTTCAAGCAGTTATCATGCCTCAGCCTCCTGAGTATCTGGGA T C ACIN1 Ensembl:ENSG00000100813 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1026916561 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109025,RMVar_hsa_circ_165293,RMVar_hsa_circ_165294,RMVar_hsa_circ_80287,RMVar_hsa_circ_165296,RMVar_hsa_circ_1989,RMVar_hsa_circ_374686,RMVar_hsa_circ_377234 46620 RMVar_ID_46620 Human_SNP_ID_547878002 A-to-I Human chr14 - 23074482 23074482 23074482 CTGCTCACTGCAACCTCCGCCTCCTGGGTTCAAGCAATTATCATGCCTCAGCCTCCTGAGTATCT CTGCTCACTGCAACCTCCGCCTCCTGGGTTCAGGCAATTATCATGCCTCAGCCTCCTGAGTATCT T C ACIN1 Ensembl:ENSG00000100813 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1191967152 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109025,RMVar_hsa_circ_165293,RMVar_hsa_circ_165294,RMVar_hsa_circ_80287,RMVar_hsa_circ_165296,RMVar_hsa_circ_1989,RMVar_hsa_circ_374686,RMVar_hsa_circ_377234 46621 RMVar_ID_46621 Human_SNP_ID_547880270 A-to-I Human chr14 - 23082712 23082712 23082712 AGAAAAACATGTGAGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGCAGATCACT AGAAAAACATGTGAGCTCATGCCTGTAATCCCGGCACTTTGGGAGGCCAAGGCGGGCAGATCACT T C ACIN1 Ensembl:ENSG00000100813 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1478525441 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12300850 RMVar_hsa_circ_165294,RMVar_hsa_circ_80287,RMVar_hsa_circ_57929,RMVar_hsa_circ_377234,RMVar_hsa_circ_99923,RMVar_hsa_circ_165300,RMVar_hsa_circ_115775,RMVar_hsa_circ_165301,RMVar_hsa_circ_165302,RMVar_hsa_circ_299719 46622 RMVar_ID_46622 Human_SNP_ID_547882606 A-to-I Human chr14 - 23091513 23091513 23091513 TAACCCAGGCTGGAGTGCAGTGGCACGATCTCAGTTCACTGCACCCACCACCTCCTGAGTAGCCA TAACCCAGGCTGGAGTGCAGTGGCACGATCTCGGTTCACTGCACCCACCACCTCCTGAGTAGCCA T C ACIN1 Ensembl:ENSG00000100813 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs937376037 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17562347 RMVar_hsa_circ_165294,RMVar_hsa_circ_80287,RMVar_hsa_circ_57929,RMVar_hsa_circ_377234 46623 RMVar_ID_46623 Human_SNP_ID_547884279 A-to-I Human chr14 + 23096689 23096689 23096689 GCCTCAACCTCCCGGGCTCAGGTGATGCTCCTACCTCAGTCTCCTACGTAGCTAGGACTACAGGT GCCTCAACCTCCCGGGCTCAGGTGATGCTCCTGCCTCAGTCTCCTACGTAGCTAGGACTACAGGT A G C14orf119 Ensembl:ENSG00000179933 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1336490732 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124089,RMVar_hsa_circ_165303 46624 RMVar_ID_46624 Human_SNP_ID_547884296 A-to-I Human chr14 + 23096742 23096742 23096742 AGGACTACAGGTAGGCACCTCTACGCTCAACTAATTTTTTTATTTTTTGTAGGGATGAGGTTTTG AGGACTACAGGTAGGCACCTCTACGCTCAACTCATTTTTTTATTTTTTGTAGGGATGAGGTTTTG A C C14orf119 Ensembl:ENSG00000179933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569023190 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124089,RMVar_hsa_circ_165303 46625 RMVar_ID_46625 Human_SNP_ID_547884297 A-to-I Human chr14 + 23096742 23096742 23096742 AGGACTACAGGTAGGCACCTCTACGCTCAACTAATTTTTTTATTTTTTGTAGGGATGAGGTTTTG AGGACTACAGGTAGGCACCTCTACGCTCAACTGATTTTTTTATTTTTTGTAGGGATGAGGTTTTG A G C14orf119 Ensembl:ENSG00000179933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569023190 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124089,RMVar_hsa_circ_165303 46626 RMVar_ID_46626 Human_SNP_ID_547893814 A-to-I Human chr14 - 23132466 23132466 23132466 GCAATCTTCCTGCTTCAGCCTCCCAAGTAGCTAGAAATATAGGTGTGTGCCACTGTGCCTGGCTT GCAATCTTCCTGCTTCAGCCTCCCAAGTAGCTGGAAATATAGGTGTGTGCCACTGTGCCTGGCTT T C SLC7A8 Ensembl:ENSG00000092068 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs957999612 Functional Loss SNV dbSNP153 33..33 33 - - - 46627 RMVar_ID_46627 Human_SNP_ID_547930248 A-to-I Human chr14 - 23277740 23277740 23277740 ACTTCTAAAGACAGATTTTTTTTTTTTTTGATAGGGTCTCACTCTATCACCCAGGCTGGAGTGCA ACTTCTAAAGACAGATTTTTTTTTTTTTTGATTGGGTCTCACTCTATCACCCAGGCTGGAGTGCA T A HOMEZ Ensembl:ENSG00000215271 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1328113003 Functional Loss SNV dbSNP153 33..33 33 - - - 46628 RMVar_ID_46628 Human_SNP_ID_547935928 A-to-I Human chr14 - 23297470 23297470 23297470 CTGAGATTTTCCCAACCCCCTGGCTTTTCCTCACCTTGGGTTGAGTTGATCCGGCACTACCACAA CTGAGATTTTCCCAACCCCCTGGCTTTTCCTCGCCTTGGGTTGAGTTGATCCGGCACTACCACAA T C PPP1R3E,HOMEZ Ensembl:ENSG00000235194,Ensembl:ENSG00000215271 Protein coding,Protein coding 3'UTR,intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs750082813 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_443743,Human_RBP_ID_757921,Human_RBP_ID_12301325,Human_RBP_ID_17076464 Human_miRNA_ID_98665,Human_miRNA_ID_189167 46629 RMVar_ID_46629 Human_SNP_ID_547940230 A-to-I Human chr14 + 23314177 23314177 23314177 CACAAGGTCAGGAGATCGTGACGGTCCTGGCTAACACAGTGAAACCCCGTCTCTACTAAAAATAC CACAAGGTCAGGAGATCGTGACGGTCCTGGCTCACACAGTGAAACCCCGTCTCTACTAAAAATAC A C BCL2L2-PABPN1 Ensembl:ENSG00000258643 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1425154554 Functional Loss SNV dbSNP153 33..33 33 - - - 46630 RMVar_ID_46630 Human_SNP_ID_547940233 A-to-I Human chr14 + 23314182 23314182 23314182 GGTCAGGAGATCGTGACGGTCCTGGCTAACACAGTGAAACCCCGTCTCTACTAAAAATACAAAAA GGTCAGGAGATCGTGACGGTCCTGGCTAACACGGTGAAACCCCGTCTCTACTAAAAATACAAAAA A G BCL2L2-PABPN1 Ensembl:ENSG00000258643 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1566464124 Functional Loss SNV dbSNP153 33..33 33 - - - 46631 RMVar_ID_46631 Human_SNP_ID_547941132 A-to-I Human chr14 + 23318252 23318252 23318252 TGGAATATAGTGTCGCGATCTTGGCTCACTGCAACCTCCACCTCCCAGGTTCAAGCCTTTCTCCT TGGAATATAGTGTCGCGATCTTGGCTCACTGCCACCTCCACCTCCCAGGTTCAAGCCTTTCTCCT A C BCL2L2-PABPN1 Ensembl:ENSG00000258643 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1401492164 Functional Loss SNV dbSNP153 33..33 33 - - - 46632 RMVar_ID_46632 Human_SNP_ID_547998306 A-to-I Human chr14 - 23523945 23523945 23523945 ACCCCAACACCAGAGCCACCTCTACCTCTCCTACCTCCCCCTCCACCCAGTGAGGAAGAGGGCCC ACCCCAACACCAGAGCCACCTCTACCTCTCCTGCCTCCCCCTCCACCCAGTGAGGAAGAGGGCCC T C ZFHX2 Ensembl:ENSG00000136367 Protein coding CDS GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs764323774 Functional Loss SNV dbSNP153 33..33 33 - - - 46633 RMVar_ID_46633 Human_SNP_ID_548119412 A-to-I Human chr14 + 23984608 23984608 23984608 CACTAGGTCAAGAGATGGAAACCATCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATAC CACTAGGTCAAGAGATGGAAACCATCCTGGCCTACATGGTGAAACCCCATCTCTACTAAAAATAC A T DHRS4L2,AL136419.1 Ensembl:ENSG00000187630,Ensembl:ENSG00000285467 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1425155932 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97330,RMVar_hsa_circ_165341 46634 RMVar_ID_46634 Human_SNP_ID_548119420 A-to-I Human chr14 + 23984633 23984633 23984633 CCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCTGAGCGAGGTGTTGT CCTGGCCAACATGGTGAAACCCCATCTCTACTGAAAATACAAAAATTAGCTGAGCGAGGTGTTGT A G DHRS4L2,AL136419.1 Ensembl:ENSG00000187630,Ensembl:ENSG00000285467 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1222591837 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5246950 RMVar_hsa_circ_97330,RMVar_hsa_circ_165341 46635 RMVar_ID_46635 Human_SNP_ID_548119439 A-to-I Human chr14 + 23984713 23984713 23984713 ACTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGGGAGGCAGAGGTT ACTGTAGTCCCAGCTACTCGGGAGGCTGAGGCTGGAGAATCGCTTGAACCCGGGAGGCAGAGGTT A T DHRS4L2,AL136419.1 Ensembl:ENSG00000187630,Ensembl:ENSG00000285467 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1410767656 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97330,RMVar_hsa_circ_165341 46636 RMVar_ID_46636 Human_SNP_ID_548119795 A-to-I Human chr14 + 23985808 23985808 23985808 ATGATCTCAGCTCACTGCAACCTCTGCCTCCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTG ATGATCTCAGCTCACTGCAACCTCTGCCTCCCTGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTG A T DHRS4L2,AL136419.1 Ensembl:ENSG00000187630,Ensembl:ENSG00000285467 Protein coding,lincRNA intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs967013177 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97330,RMVar_hsa_circ_165341 46637 RMVar_ID_46637 Human_SNP_ID_548119871 A-to-I Human chr14 + 23986077 23986077 23986077 ACGAGGTTTCATCATCTCAGCCAGCTGGTCTCAAACTCCTGACCTCAAGTGATCTGCCCACCTCA ACGAGGTTTCATCATCTCAGCCAGCTGGTCTCCAACTCCTGACCTCAAGTGATCTGCCCACCTCA A C DHRS4L2,AL136419.1 Ensembl:ENSG00000187630,Ensembl:ENSG00000285467 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1321310663 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8182483 RMVar_hsa_circ_97330,RMVar_hsa_circ_165341 46638 RMVar_ID_46638 Human_SNP_ID_548122869 A-to-I Human chr14 + 23994535 23994535 23994535 CATGGCAAGACCCTGTCTCTACAAAAAATACAAAAATTGCCCGGGTGTGGTGGCACGCACTTCTA CATGGCAAGACCCTGTCTCTACAAAAAATACAGAAATTGCCCGGGTGTGGTGGCACGCACTTCTA A G DHRS4L2,AL136419.1 Ensembl:ENSG00000187630,Ensembl:ENSG00000285467 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs567317704 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97330,RMVar_hsa_circ_165341 46639 RMVar_ID_46639 Human_SNP_ID_548154921 A-to-I Human chr14 - 24107740 24107740 24107740 AAATATGGCTGTTTTGCAATCCCTAGTGAGTTAATGCATTTAGACACTGAACATCTGAGTCTGGA AAATATGGCTGTTTTGCAATCCCTAGTGAGTTGATGCATTTAGACACTGAACATCTGAGTCTGGA T C NRL Ensembl:ENSG00000129535 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223060825 Functional Loss SNV dbSNP153 33..33 33 - - - 46640 RMVar_ID_46640 Human_SNP_ID_548155070 A-to-I Human chr14 + 24108438 24108438 24108438 CAGCTCACTGCAGCCTTGAATTCCTGGGCTCAAATGATCCTCTTGCCTCAGCCTCCCGAGTAGCT CAGCTCACTGCAGCCTTGAATTCCTGGGCTCATATGATCCTCTTGCCTCAGCCTCCCGAGTAGCT A T PCK2 Ensembl:ENSG00000100889 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1433776878 Functional Loss SNV dbSNP153 33..33 33 - - - 46641 RMVar_ID_46641 Human_SNP_ID_548159899 A-to-I Human chr14 + 24126496 24126496 24126496 TCTGCCTCCCCCTGGACTCAAGCGATCCTCCCACTTCAGCCTCCCAAGTAGCTGGGACTACCAGC TCTGCCTCCCCCTGGACTCAAGCGATCCTCCCGCTTCAGCCTCCCAAGTAGCTGGGACTACCAGC A G AL136295.3 Ensembl:ENSG00000259371 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1271186263 Functional Loss SNV dbSNP153 33..33 33 - - - 46642 RMVar_ID_46642 Human_SNP_ID_548168185 A-to-I Human chr14 + 24153836 24153836 24153836 TGAGGCAGGAAAATCTCTTGAACCTGGGAGACAGAGGTTGCAGTGAGCCAGGATTGCGCCACAGC TGAGGCAGGAAAATCTCTTGAACCTGGGAGACGGAGGTTGCAGTGAGCCAGGATTGCGCCACAGC A G RNF31,AL136295.5 Ensembl:ENSG00000092098,Ensembl:ENSG00000259529 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs924744185 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22473141 RMVar_hsa_circ_89140,RMVar_hsa_circ_79635,RMVar_hsa_circ_165371,RMVar_hsa_circ_165372 46643 RMVar_ID_46643 Human_SNP_ID_548168284 A-to-I Human chr14 + 24154124 24154124 24154124 TCAAGCGATTCTCCTGTCCCAGCCTCCCAAGTAGCTGTGATTACAGGCATCTGCAATCATGCCCG TCAAGCGATTCTCCTGTCCCAGCCTCCCAAGTGGCTGTGATTACAGGCATCTGCAATCATGCCCG A G RNF31,AL136295.5 Ensembl:ENSG00000092098,Ensembl:ENSG00000259529 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs904797331 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89140,RMVar_hsa_circ_79635,RMVar_hsa_circ_165371,RMVar_hsa_circ_165372 46644 RMVar_ID_46644 Human_SNP_ID_548168386 A-to-I Human chr14 + 24154506 24154506 24154506 CACAATGTTGGCCAGGCTGGTCTCGAACTCCTAGCCTCAAGTGATGCGCCCGCCTTGGCTTCCCA CACAATGTTGGCCAGGCTGGTCTCGAACTCCTGGCCTCAAGTGATGCGCCCGCCTTGGCTTCCCA A G RNF31,AL136295.5 Ensembl:ENSG00000092098,Ensembl:ENSG00000259529 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1395699889 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17562359,Human_RBP_ID_22711646 RMVar_hsa_circ_89140,RMVar_hsa_circ_79635,RMVar_hsa_circ_165371,RMVar_hsa_circ_165372 46645 RMVar_ID_46645 Human_SNP_ID_548173134 A-to-I Human chr14 + 24170668 24170668 24170668 TTCTTCAGCTGGGGGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGCGG TTCTTCAGCTGGGGGCAGTGGCTCACGCCTGTGATCCCAGCACTTTGGGAGGCCAAGGCGGGCGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924172685 Functional Loss SNV dbSNP153 33..33 33 - - - 46646 RMVar_ID_46646 Human_SNP_ID_548176418 A-to-I Human chr14 - 24180443 24180443 24180443 TCAGGAGCTCCAGGCTGTACTGGGCCTCTCCTAGACTGCAGGCTGCAGCCAGTCCAGAGAGAATA TCAGGAGCTCCAGGCTGTACTGGGCCTCTCCTGGACTGCAGGCTGCAGCCAGTCCAGAGAGAATA T C IPO4,AL136295.4 Ensembl:ENSG00000196497,Ensembl:ENSG00000259522 Protein coding,Protein coding stop codon,3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1471263219 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17651334 Human_miRNA_ID_2332349,Human_miRNA_ID_2545857,Human_miRNA_ID_2965435 RMVar_hsa_circ_120192,RMVar_hsa_circ_165378 46647 RMVar_ID_46647 Human_SNP_ID_548182908 A-to-I Human chr14 + 24199436 24199436 24199436 TCCCTGCTTCCCCTTCACCTTCCGTTTTGATTATAAGCTTCCTGAGGCCTCCCCAGAAGCTGAGC TCCCTGCTTCCCCTTCACCTTCCGTTTTGATTGTAAGCTTCCTGAGGCCTCCCCAGAAGCTGAGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1212498676 Functional Loss SNV dbSNP153 33..33 33 - - - 46648 RMVar_ID_46648 Human_SNP_ID_548183662 A-to-I Human chr14 + 24201670 24201670 24201670 GGCTGTGGTTCTGCAGGCTGTACAGGAAGCATAATGCTGGCATCTGCTTCTGGGGAGGCCTCAGG GGCTGTGGTTCTGCAGGCTGTACAGGAAGCATGATGCTGGCATCTGCTTCTGGGGAGGCCTCAGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1246404222 Functional Loss SNV dbSNP153 33..33 33 - - - 46649 RMVar_ID_46649 Human_SNP_ID_548185744 A-to-I Human chr14 - 24208770 24208770 24208770 CGGCTCACTGCAACCCCTGCATCCCGGGTTCAAGTGATTCTCCTGCCTCAGCCAGGTGCCACTAT CGGCTCACTGCAACCCCTGCATCCCGGGTTCAGGTGATTCTCCTGCCTCAGCCAGGTGCCACTAT T C AL136295.1 Ensembl:ENSG00000254692 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs986266718 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6335541,Human_RBP_ID_12304890 RMVar_hsa_circ_125406,RMVar_hsa_circ_165388 46650 RMVar_ID_46650 Human_SNP_ID_548188761 A-to-I Human chr14 - 24219251 24219251 24219251 CGCTGTGTTGTCCAGGCTGGTCTGGAACTCCTAGGCTCAAGTGATCCTCCCGCCTCAGTCTCCCA CGCTGTGTTGTCCAGGCTGGTCTGGAACTCCTGGGCTCAAGTGATCCTCCCGCCTCAGTCTCCCA T C NEDD8-MDP1,NEDD8 Ensembl:ENSG00000255526,Ensembl:ENSG00000129559 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1258126886 Functional Loss SNV dbSNP153 33..33 33 - - - 46651 RMVar_ID_46651 Human_SNP_ID_548188808 A-to-I Human chr14 - 24219400 24219400 24219400 CTTACTGCTGCTGCCTCTAATTTCTGGACTCAAGTGATCCTCCCACCTCAGCCTCCCAAATAGCT CTTACTGCTGCTGCCTCTAATTTCTGGACTCAGGTGATCCTCCCACCTCAGCCTCCCAAATAGCT T C NEDD8-MDP1,NEDD8 Ensembl:ENSG00000255526,Ensembl:ENSG00000129559 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1442583462 Functional Loss SNV dbSNP153 33..33 33 - - - 46652 RMVar_ID_46652 Human_SNP_ID_548189008 A-to-I Human chr14 - 24219973 24219973 24219973 CACCACGCCTGGCTAATTTTGTATTTTTTAATAGAGAAGGCTTTCTCCATGTTGGCCAGGCTGGT CACCACGCCTGGCTAATTTTGTATTTTTTAATGGAGAAGGCTTTCTCCATGTTGGCCAGGCTGGT T C NEDD8-MDP1,NEDD8 Ensembl:ENSG00000255526,Ensembl:ENSG00000129559 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1162497090 Functional Loss SNV dbSNP153 33..33 33 - - - 46653 RMVar_ID_46653 Human_SNP_ID_548189009 A-to-I Human chr14 - 24219976 24219976 24219976 CGCCACCACGCCTGGCTAATTTTGTATTTTTTAATAGAGAAGGCTTTCTCCATGTTGGCCAGGCT CGCCACCACGCCTGGCTAATTTTGTATTTTTTGATAGAGAAGGCTTTCTCCATGTTGGCCAGGCT T C NEDD8-MDP1,NEDD8 Ensembl:ENSG00000255526,Ensembl:ENSG00000129559 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1476086236 Functional Loss SNV dbSNP153 33..33 33 - - - 46654 RMVar_ID_46654 Human_SNP_ID_548189011 A-to-I Human chr14 - 24219991 24219991 24219991 GGGATTACAGGCATGCGCCACCACGCCTGGCTAATTTTGTATTTTTTAATAGAGAAGGCTTTCTC GGGATTACAGGCATGCGCCACCACGCCTGGCTGATTTTGTATTTTTTAATAGAGAAGGCTTTCTC T C NEDD8-MDP1,NEDD8 Ensembl:ENSG00000255526,Ensembl:ENSG00000129559 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs755260887 Functional Loss SNV dbSNP153 33..33 33 - - - 46655 RMVar_ID_46655 Human_SNP_ID_548189127 A-to-I Human chr14 - 24220568 24220568 24220568 CCTGTAATCCCAGCTCTTTGGGAGGCCGAGGCAGGAGGATCACTTGAGCCCATGAGTTTGAAACC CCTGTAATCCCAGCTCTTTGGGAGGCCGAGGCGGGAGGATCACTTGAGCCCATGAGTTTGAAACC T C NEDD8-MDP1,NEDD8 Ensembl:ENSG00000255526,Ensembl:ENSG00000129559 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982586532 Functional Loss SNV dbSNP153 33..33 33 - - - 46656 RMVar_ID_46656 Human_SNP_ID_548189692 A-to-I Human chr14 - 24223004 24223004 24223004 TCAGCTCACCGTAACCTCCGCCTCCTGGGTTCAGGCGATTCTCCTGCCTCAGCCTCCCCAGTAGC TCAGCTCACCGTAACCTCCGCCTCCTGGGTTCTGGCGATTCTCCTGCCTCAGCCTCCCCAGTAGC T A NEDD8-MDP1,NEDD8 Ensembl:ENSG00000255526,Ensembl:ENSG00000129559 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs997660964 Functional Loss SNV dbSNP153 33..33 33 - - - 46657 RMVar_ID_46657 Human_SNP_ID_548189767 A-to-I Human chr14 - 24223220 24223218 24223220 GCTAATTTTATTGTAGAGATGGGGATCTCACTATGTTGCCCAGGCTGGTCTCAAAACTCCAAGCC GCTAATTTTATTGTAGAGATGGGGATCTCACT__GTTGCCCAGGCTGGTCTCAAAACTCCAAGCC CAT C NEDD8-MDP1,NEDD8 Ensembl:ENSG00000255526,Ensembl:ENSG00000129559 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1291952621 Functional Loss DEL dbSNP153 33..34 33 - - - 46658 RMVar_ID_46658 Human_SNP_ID_548189768 A-to-I Human chr14 - 24223220 24223220 24223220 GCTAATTTTATTGTAGAGATGGGGATCTCACTATGTTGCCCAGGCTGGTCTCAAAACTCCAAGCC GCTAATTTTATTGTAGAGATGGGGATCTCACTGTGTTGCCCAGGCTGGTCTCAAAACTCCAAGCC T C NEDD8-MDP1,NEDD8 Ensembl:ENSG00000255526,Ensembl:ENSG00000129559 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs564925672 Functional Loss SNV dbSNP153 33..33 33 - - - 46659 RMVar_ID_46659 Human_SNP_ID_548189787 A-to-I Human chr14 - 24223341 24223328 24223341 AAGCTGGAGTGCAGTGGCACAATCAGCCCACTACGGCATTGAACTCCTGGGCTTGGGCAGTCTTG AAGCTGGAGTGCAGTGGCACAATCAGCCCACT_____________CCTGGGCTTGGGCAGTCTTG GAGTTCAATGCCGT G NEDD8-MDP1,NEDD8 Ensembl:ENSG00000255526,Ensembl:ENSG00000129559 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs962943211 Functional Loss DEL dbSNP153 33..45 33 - - - Human_RBP_ID_6335609,Human_RBP_ID_12305135 46660 RMVar_ID_46660 Human_SNP_ID_548189794 A-to-I Human chr14 - 24223352 24223352 24223352 CTCTGTCACCCAAGCTGGAGTGCAGTGGCACAATCAGCCCACTACGGCATTGAACTCCTGGGCTT CTCTGTCACCCAAGCTGGAGTGCAGTGGCACAGTCAGCCCACTACGGCATTGAACTCCTGGGCTT T C NEDD8-MDP1,NEDD8 Ensembl:ENSG00000255526,Ensembl:ENSG00000129559 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs535523627 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6335609,Human_RBP_ID_12460536,Human_RBP_ID_17562811 46661 RMVar_ID_46661 Human_SNP_ID_548191508 A-to-I Human chr14 - 24229905 24229905 24229905 CACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAAACGGGGTTTCACCAGGTTGGCCAGGATGG CACCACGCCCAGCTAATTTTTGTATTTTTAGTCGAAACGGGGTTTCACCAGGTTGGCCAGGATGG T G NEDD8-MDP1,NEDD8 Ensembl:ENSG00000255526,Ensembl:ENSG00000129559 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1200451746 Functional Loss SNV dbSNP153 33..33 33 - - - 46662 RMVar_ID_46662 Human_SNP_ID_548195791 A-to-I Human chr14 + 24243606 24243606 24243606 GCGTAGTGGCACGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGTTGGGAGGATTGTTTGAGCCAG GCGTAGTGGCACGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGTTGGGAGGATTGTTTGAGCCAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1487135462 Functional Loss SNV dbSNP153 33..33 33 - - - 46663 RMVar_ID_46663 Human_SNP_ID_548250578 A-to-I Human chr14 + 24439794 24439794 24439794 AAGGTTAGTGAGACAATTTATTTTTATTGCCTAAACTGCAGAGCATTCTCTACACAGCGTAAAGG AAGGTTAGTGAGACAATTTATTTTTATTGCCTGAACTGCAGAGCATTCTCTACACAGCGTAAAGG A G KHNYN Ensembl:ENSG00000100441 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1001776218 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6335927,Human_RBP_ID_8181415,Human_RBP_ID_8794043,Human_RBP_ID_17846924,Human_RBP_ID_18272602,Human_RBP_ID_26431618 46664 RMVar_ID_46664 Human_SNP_ID_548356758 A-to-I Human chr14 - 24838139 24838139 24838139 AGGAGTAGTGGCATGCACCTATAATCCCAGCTACTTGGGAGGCTGAGGTGGGAGGATCATTGCTA AGGAGTAGTGGCATGCACCTATAATCCCAGCTCCTTGGGAGGCTGAGGTGGGAGGATCATTGCTA T G STXBP6 Ensembl:ENSG00000168952 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1566397146 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_165445,RMVar_hsa_circ_349828 46665 RMVar_ID_46665 Human_SNP_ID_548760830 A-to-I Human chr14 - 26458596 26458596 26458596 CCATGTTTACTCAGTGTTTAGTTCCCTCTCATAAGGGAGAACAAGCAGTATTTGGCTTTCTGTTT CCATGTTTACTCAGTGTTTAGTTCCCTCTCATTAGGGAGAACAAGCAGTATTTGGCTTTCTGTTT T A NOVA1 Ensembl:ENSG00000139910 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1028972159 Functional Loss SNV dbSNP153 33..33 33 - - - 46666 RMVar_ID_46666 Human_SNP_ID_548787106 A-to-I Human chr14 - 26570284 26570284 26570284 GGAGTGCAGTGGCGCGATCATGGCTCACTGCAACCTCTGCCTCCCAGGTTCAAGCTGTTTTCCTG GGAGTGCAGTGGCGCGATCATGGCTCACTGCAGCCTCTGCCTCCCAGGTTCAAGCTGTTTTCCTG T C NOVA1 Ensembl:ENSG00000139910 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1414566242 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5984 46667 RMVar_ID_46667 Human_SNP_ID_549206306 A-to-I Human chr14 - 28264614 28264614 28264614 ACTGCCCCCTTTCCCATTATTGCTAAAGTGCAATTCTACCCAGGAGCCCTGCAGGCTCTCCTCCT ACTGCCCCCTTTCCCATTATTGCTAAAGTGCAGTTCTACCCAGGAGCCCTGCAGGCTCTCCTCCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1198088670 Functional Loss SNV dbSNP153 33..33 33 - - - 46668 RMVar_ID_46668 Human_SNP_ID_549206308 A-to-I Human chr14 - 28264622 28264622 28264622 GCTGGAACACTGCCCCCTTTCCCATTATTGCTAAAGTGCAATTCTACCCAGGAGCCCTGCAGGCT GCTGGAACACTGCCCCCTTTCCCATTATTGCTGAAGTGCAATTCTACCCAGGAGCCCTGCAGGCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270768105 Functional Loss SNV dbSNP153 33..33 33 - - - 46669 RMVar_ID_46669 Human_SNP_ID_549206345 A-to-I Human chr14 + 28264763 28264763 28264763 AAGAGTTCTCACTGTGACAGCCCACCTCGCTCACAGACACCACAAGATACCAACAGAGCTTCTGA AAGAGTTCTCACTGTGACAGCCCACCTCGCTCGCAGACACCACAAGATACCAACAGAGCTTCTGA A G BNIP3P1 Ensembl:ENSG00000197358 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1339450406 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1084923,Human_RBP_ID_8250610 Human_miRNA_ID_1878128 46670 RMVar_ID_46670 Human_SNP_ID_549545653 A-to-I Human chr14 - 29614905 29614905 29614905 TAGTTCAAGACCAGCCTGGGCAACATGGCGAAACCCTGTCTCTACTAAAAATACAAAAAAAAAAA TAGTTCAAGACCAGCCTGGGCAACATGGCGAAGCCCTGTCTCTACTAAAAATACAAAAAAAAAAA T C PRKD1 Ensembl:ENSG00000184304 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1031480764 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_120570 RMVar_hsa_circ_102867,RMVar_hsa_circ_345793,RMVar_hsa_circ_349812,RMVar_hsa_circ_315262,RMVar_hsa_circ_165483,RMVar_hsa_circ_165482,RMVar_hsa_circ_316825,RMVar_hsa_circ_8204 46671 RMVar_ID_46671 Human_SNP_ID_549545657 A-to-I Human chr14 - 29614915 29614915 29614915 CTGAGCTCAGTAGTTCAAGACCAGCCTGGGCAACATGGCGAAACCCTGTCTCTACTAAAAATACA CTGAGCTCAGTAGTTCAAGACCAGCCTGGGCAGCATGGCGAAACCCTGTCTCTACTAAAAATACA T C PRKD1 Ensembl:ENSG00000184304 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs958087427 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_120570 RMVar_hsa_circ_102867,RMVar_hsa_circ_345793,RMVar_hsa_circ_349812,RMVar_hsa_circ_315262,RMVar_hsa_circ_165483,RMVar_hsa_circ_165482,RMVar_hsa_circ_316825,RMVar_hsa_circ_8204 46672 RMVar_ID_46672 Human_SNP_ID_144158548 A-to-I Human chr3 + 93981758 93981758 93981758 TAAACGGGCACGGTGACGCACGCCTGTAGTCCAAGCTACTTCGGAGGCTGAATCAGTAGGATCAC TAAACGGGCACGGTGACGCACGCCTGTAGTCCGAGCTACTTCGGAGGCTGAATCAGTAGGATCAC A G ARL13B Ensembl:ENSG00000169379 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041914775 Functional Loss SNV dbSNP153 33..33 33 - - - 46673 RMVar_ID_46673 Human_SNP_ID_144178499 A-to-I Human chr3 - 94059360 94059360 94059360 AAGATACAAAAATTGGCTGGGCATTGTGGCACACACCTGTAGTCTCGTCTACTCACGGGGCTGAG AAGATACAAAAATTGGCTGGGCATTGTGGCACGCACCTGTAGTCTCGTCTACTCACGGGGCTGAG T C DHFR2 Ensembl:ENSG00000178700 Protein coding intron GSE47997;GSE99789;GSE123020:GSM3490829,GSM3490830,GSM3490831 K562 cells&HepG2 cells;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109 cell line - 23474544,29796672,32596459 RNA-Seq:(High) rs1380396674 Functional Loss SNV dbSNP153 33..33 33 - - - 46674 RMVar_ID_46674 Human_SNP_ID_144178522 A-to-I Human chr3 - 94059495 94059495 94059495 GAAAGAAGTAGAGAGAGAATTAAAAACTGGCCAGGAGTGGTGGCTCACGCCTGTGGTCCCAGCAC GAAAGAAGTAGAGAGAGAATTAAAAACTGGCCGGGAGTGGTGGCTCACGCCTGTGGTCCCAGCAC T C DHFR2 Ensembl:ENSG00000178700 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs11545822 Functional Loss SNV dbSNP153 33..33 33 - - - 46675 RMVar_ID_46675 Human_SNP_ID_144182439 A-to-I Human chr3 - 94076151 94076151 94076151 TTCCAGTGGTACTGATCGCAGACTGAATGTCTAGGATTTAAGTAAAATTGGAGAGGAACAATCCC TTCCAGTGGTACTGATCGCAGACTGAATGTCTGGGATTTAAGTAAAATTGGAGAGGAACAATCCC T C RBBP4P2 Ensembl:ENSG00000242457 Pseudogene exon GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1443813115 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1887024 46676 RMVar_ID_46676 Human_SNP_ID_144194536 A-to-I Human chr3 + 94127965 94127965 94127965 GCTAAAGTCCAGGCACGGTGGCTTATGCCTGTAATCCCAGCACTTTGTCAGGCCGAGGCAGGGGG GCTAAAGTCCAGGCACGGTGGCTTATGCCTGTGATCCCAGCACTTTGTCAGGCCGAGGCAGGGGG A G NSUN3 Ensembl:ENSG00000178694 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,31158229,31158229,31158229,31158229,31158229,31158229 RNA-Seq:(High) rs972603590 Functional Loss SNV dbSNP153 33..33 33 - - - 46677 RMVar_ID_46677 Human_SNP_ID_144808491 A-to-I Human chr3 - 96350548 96350548 96350548 ATCAGCACTGAAACCAACCATGCCATGGTAACAGTCTCCAGGTCTCCCTCTTCTGTCATAGGCCA ATCAGCACTGAAACCAACCATGCCATGGTAACGGTCTCCAGGTCTCCCTCTTCTGTCATAGGCCA T C lnc-MTRNR2L12-9 RNACentral:URS00009BA044 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878860346 Functional Loss SNV dbSNP153 33..33 33 - - - 46678 RMVar_ID_46678 Human_SNP_ID_144808493 A-to-I Human chr3 - 96350556 96350556 96350556 CAAGTTTCATCAGCACTGAAACCAACCATGCCATGGTAACAGTCTCCAGGTCTCCCTCTTCTGTC CAAGTTTCATCAGCACTGAAACCAACCATGCCGTGGTAACAGTCTCCAGGTCTCCCTCTTCTGTC T C lnc-MTRNR2L12-9 RNACentral:URS00009BA044 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879110177 Functional Loss SNV dbSNP153 33..33 33 - - - 46679 RMVar_ID_46679 Human_SNP_ID_145215353 A-to-I Human chr3 + 97944882 97944882 97944882 TAAAGAAGTTGTTTCTTCCAAAGAACAAAGCCAGGTTAATGACATTCAATTCTAAATGATACATT TAAAGAAGTTGTTTCTTCCAAAGAACAAAGCCTGGTTAATGACATTCAATTCTAAATGATACATT A T CRYBG3 Ensembl:ENSG00000080200 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1559753690 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_457598 46680 RMVar_ID_46680 Human_SNP_ID_145375254 A-to-I Human chr3 + 98525182 98525182 98525182 AGATATCTGCTGCATCGAACTTTAAACTTCACATTGTCCTTATTTTTCTTGATCTTGACAGATTC AGATATCTGCTGCATCGAACTTTAAACTTCACGTTGTCCTTATTTTTCTTGATCTTGACAGATTC A G AC021660.2 Ensembl:ENSG00000248839 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355407241 Functional Loss SNV dbSNP153 33..33 33 - - - 46681 RMVar_ID_46681 Human_SNP_ID_145375273 A-to-I Human chr3 + 98525242 98525242 98525242 GATTCAGCATCCTTTCATTGGGCTGTGAACAGAAAGTCCTTGATTTCCTCAATTTTCGGAGGCAT GATTCAGCATCCTTTCATTGGGCTGTGAACAGGAAGTCCTTGATTTCCTCAATTTTCGGAGGCAT A G AC021660.2 Ensembl:ENSG00000248839 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1044870147 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_458014 46682 RMVar_ID_46682 Human_SNP_ID_145433092 A-to-I Human chr3 - 98748590 98748590 98748590 CATGGTGGCAGGCGCCTGTAATTCCAGCTACTAGGGAGGCTGAGGCAAGAGAAACGCTTAAACCC CATGGTGGCAGGCGCCTGTAATTCCAGCTACTGGGGAGGCTGAGGCAAGAGAAACGCTTAAACCC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1293211713 Functional Loss SNV dbSNP153 33..33 33 - - - 46683 RMVar_ID_46683 Human_SNP_ID_145487427 A-to-I Human chr3 + 98969827 98969827 98969827 TCACACCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTGCAGGCGCCCGCCACCATGCCCG TCACACCATTCTCCTGCCTCAGCCTCCCGAGTGGCTGGGACTGCAGGCGCCCGCCACCATGCCCG A G AC091212.1 Ensembl:ENSG00000239462 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs570312359 Functional Loss SNV dbSNP153 33..33 33 - - - 46684 RMVar_ID_46684 Human_SNP_ID_145618648 A-to-I Human chr3 - 99450153 99450153 99450153 AAACAGTGTAGTACTGGCCTAAAAACAGACACAAAGACCAATGGAACAGAACAGAGAACCCAGAA AAACAGTGTAGTACTGGCCTAAAAACAGACACGAAGACCAATGGAACAGAACAGAGAACCCAGAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs562814377 Functional Loss SNV dbSNP153 33..33 33 - - - 46685 RMVar_ID_46685 Human_SNP_ID_145694780 A-to-I Human chr3 + 99751333 99751333 99751333 TAATCCCAGCAATATAGGAGGCCAAAGCGGGCAGATCACCTGAGGTCAGGAGTTTGAGACCAGCC TAATCCCAGCAATATAGGAGGCCAAAGCGGGCGGATCACCTGAGGTCAGGAGTTTGAGACCAGCC A G COL8A1 Ensembl:ENSG00000144810 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1376794839 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100127,RMVar_hsa_circ_219966 46686 RMVar_ID_46686 Human_SNP_ID_145712185 A-to-I Human chr3 + 99825983 99825983 99825983 GTATTTTTAGTAGAGGGGGGTTTCACCACGTTAGGCAGGATGGTCTTGATCTCCTGTCCTCATGA GTATTTTTAGTAGAGGGGGGTTTCACCACGTTGGGCAGGATGGTCTTGATCTCCTGTCCTCATGA A G CMSS1 Ensembl:ENSG00000184220 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs989623738 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8580868 RMVar_hsa_circ_92133,RMVar_hsa_circ_219968 46687 RMVar_ID_46687 Human_SNP_ID_145726017 A-to-I Human chr3 + 99887758 99887758 99887758 TATAGATATGGATATGATGTAGATATTGAGATAGGGCCTCATTCTGTCACCCAGGCTGGAGTGCA TATAGATATGGATATGATGTAGATATTGAGATGGGGCCTCATTCTGTCACCCAGGCTGGAGTGCA A G CMSS1 Ensembl:ENSG00000184220 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs575801983 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8580964 RMVar_hsa_circ_92133,RMVar_hsa_circ_219968 46688 RMVar_ID_46688 Human_SNP_ID_145802667 A-to-I Human chr3 - 100225548 100225548 100225548 TGCATAACGTAGCTCCTCCTCCATCTCTGCCAACGTTTCATTTGCTTCCTGTTGCTTTTCATCAA TGCATAACGTAGCTCCTCCTCCATCTCTGCCAGCGTTTCATTTGCTTCCTGTTGCTTTTCATCAA T C AC129803.1 Ensembl:ENSG00000287378 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs566185983 Functional Loss SNV dbSNP153 33..33 33 - - - 46689 RMVar_ID_46689 Human_SNP_ID_145818074 A-to-I Human chr3 + 100291417 100291415 100291417 CAAGCCTGGCCAACATGGCGAAACTTGTCTCTACTAAAAATACAAAAATTAGTCGGGTGTGGTGG CAAGCCTGGCCAACATGGCGAAACTTGTCTC__CTAAAAATACAAAAATTAGTCGGGTGTGGTGG CTA C TBC1D23 Ensembl:ENSG00000036054 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1280087700 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_9941,RMVar_hsa_circ_49130,RMVar_hsa_circ_64093,RMVar_hsa_circ_337129,RMVar_hsa_circ_87777,RMVar_hsa_circ_219975,RMVar_hsa_circ_219976,RMVar_hsa_circ_325067,RMVar_hsa_circ_328463,RMVar_hsa_circ_328231,RMVar_hsa_circ_298000,RMVar_hsa_circ_219978,RMVar_hsa_circ_219977,RMVar_hsa_circ_10667,RMVar_hsa_circ_265143,RMVar_hsa_circ_284657,RMVar_hsa_circ_19954,RMVar_hsa_circ_219982 46690 RMVar_ID_46690 Human_SNP_ID_145822648 A-to-I Human chr3 + 100309673 100309673 100309673 TCGCTCTGTCGCGCAGACTGGAGTGCAGTGGTACAATCTCAGCACACTGCAACCTCCACCTCACA TCGCTCTGTCGCGCAGACTGGAGTGCAGTGGTGCAATCTCAGCACACTGCAACCTCCACCTCACA A G TBC1D23 Ensembl:ENSG00000036054 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1367287691 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3149,RMVar_hsa_circ_87777,RMVar_hsa_circ_219975,RMVar_hsa_circ_219976,RMVar_hsa_circ_325067,RMVar_hsa_circ_328231,RMVar_hsa_circ_10667,RMVar_hsa_circ_265143,RMVar_hsa_circ_353633,RMVar_hsa_circ_3990,RMVar_hsa_circ_269238,RMVar_hsa_circ_36514,RMVar_hsa_circ_55953,RMVar_hsa_circ_62375 46691 RMVar_ID_46691 Human_SNP_ID_145823878 A-to-I Human chr3 + 100314613 100314613 100314613 CATAGCAAGATCCTGTCTCTGAAAAAATAAAAAAATTAGGCAGGCGTAGTGGCACACCCCCGTGG CATAGCAAGATCCTGTCTCTGAAAAAATAAAAGAATTAGGCAGGCGTAGTGGCACACCCCCGTGG A G TBC1D23 Ensembl:ENSG00000036054 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs887859103 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14542972 RMVar_hsa_circ_3149,RMVar_hsa_circ_87777,RMVar_hsa_circ_219975,RMVar_hsa_circ_219976,RMVar_hsa_circ_325067,RMVar_hsa_circ_328231,RMVar_hsa_circ_10667,RMVar_hsa_circ_353633,RMVar_hsa_circ_3990,RMVar_hsa_circ_269238,RMVar_hsa_circ_15606,RMVar_hsa_circ_55953,RMVar_hsa_circ_71838,RMVar_hsa_circ_62375,RMVar_hsa_circ_65284,RMVar_hsa_circ_219991,RMVar_hsa_circ_121560 46692 RMVar_ID_46692 Human_SNP_ID_145824503 A-to-I Human chr3 + 100317057 100317057 100317057 TGAGCCAAGATCATGCTACTACATTCCAGCCTAGGTGACACAGCAAGACTCTGTCTCAAAAAAAA TGAGCCAAGATCATGCTACTACATTCCAGCCTGGGTGACACAGCAAGACTCTGTCTCAAAAAAAA A G TBC1D23 Ensembl:ENSG00000036054 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs899713611 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7096604 RMVar_hsa_circ_3149,RMVar_hsa_circ_87777,RMVar_hsa_circ_219975,RMVar_hsa_circ_219976,RMVar_hsa_circ_325067,RMVar_hsa_circ_328231,RMVar_hsa_circ_10667,RMVar_hsa_circ_353633,RMVar_hsa_circ_3990,RMVar_hsa_circ_219992,RMVar_hsa_circ_15606,RMVar_hsa_circ_55953,RMVar_hsa_circ_62375,RMVar_hsa_circ_65284,RMVar_hsa_circ_219994,RMVar_hsa_circ_273866,RMVar_hsa_circ_295321,RMVar_hsa_circ_219993 46693 RMVar_ID_46693 Human_SNP_ID_145836946 A-to-I Human chr3 + 100368810 100368810 100368810 GTTGGTCAGGAGGGTTTCGAACTCCCAACCTCAGATGATCTGCCTGCCTCGGCCTCCCAAAGTAC GTTGGTCAGGAGGGTTTCGAACTCCCAACCTCTGATGATCTGCCTGCCTCGGCCTCCCAAAGTAC A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs761877988 Functional Loss SNV dbSNP153 33..33 33 - - - 46694 RMVar_ID_46694 Human_SNP_ID_145837156 A-to-I Human chr3 + 100369600 100369600 100369600 TCTGTTTTCTGCAACCTCCGCCTCTTGGGTTCAAGTGATCCCCCTGCCTCAGCCTCCTGAGTAGC TCTGTTTTCTGCAACCTCCGCCTCTTGGGTTCCAGTGATCCCCCTGCCTCAGCCTCCTGAGTAGC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1411442466 Functional Loss SNV dbSNP153 33..33 33 - - - 46695 RMVar_ID_46695 Human_SNP_ID_145839662 A-to-I Human chr3 - 100379919 100379919 100379919 TAACTTTTTAAATTTTTTTAAGAGACAGGGTCAGGTCAGACATGGTGGCTCATGCCTGTAATCCC TAACTTTTTAAATTTTTTTAAGAGACAGGGTCGGGTCAGACATGGTGGCTCATGCCTGTAATCCC T C TOMM70 Ensembl:ENSG00000154174 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1559832323 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113778,RMVar_hsa_circ_96874,RMVar_hsa_circ_220007,RMVar_hsa_circ_220008,RMVar_hsa_circ_220009,RMVar_hsa_circ_317698,RMVar_hsa_circ_220010,RMVar_hsa_circ_293332,RMVar_hsa_circ_46953,RMVar_hsa_circ_286806,RMVar_hsa_circ_220013,RMVar_hsa_circ_119266,RMVar_hsa_circ_45012,RMVar_hsa_circ_38417,RMVar_hsa_circ_220014,RMVar_hsa_circ_220015,RMVar_hsa_circ_68038,RMVar_hsa_circ_283251,RMVar_hsa_circ_220016 46696 RMVar_ID_46696 Human_SNP_ID_146076640 A-to-I Human chr3 - 101365552 101365552 101365552 TGGCTCACTGCAACCTCCCCCTCCTGGGCTCAAGTAATCTCCTTAATCAGCCTCCCAAGTAGCTG TGGCTCACTGCAACCTCCCCCTCCTGGGCTCACGTAATCTCCTTAATCAGCCTCCCAAGTAGCTG T G SENP7 Ensembl:ENSG00000138468 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1308299324 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_258,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_14556,RMVar_hsa_circ_5955,RMVar_hsa_circ_11536,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_31533,RMVar_hsa_circ_220053,RMVar_hsa_circ_220054,RMVar_hsa_circ_220055,RMVar_hsa_circ_334177,RMVar_hsa_circ_375424,RMVar_hsa_circ_72077,RMVar_hsa_circ_220056,RMVar_hsa_circ_220057 46697 RMVar_ID_46697 Human_SNP_ID_146087442 A-to-I Human chr3 + 101414325 101414325 101414325 GGAAGATGCAGGGTCTCATGTTCCGGTGCAGCACCAGCTGCTGTGAGGACAGCCAGGCCTCCCTG GGAAGATGCAGGGTCTCATGTTCCGGTGCAGCGCCAGCTGCTGTGAGGACAGCCAGGCCTCCCTG A G AC110994.2 Ensembl:ENSG00000232830 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1477780869 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1827017 46698 RMVar_ID_46698 Human_SNP_ID_146098628 A-to-I Human chr3 + 101457649 101457649 101457649 GTGGCTGTTCTATGAACCACCTTCTTCCTTCTACGAGCAGTTCCTTTCCCACCAATGCACACTTG GTGGCTGTTCTATGAACCACCTTCTTCCTTCTGCGAGCAGTTCCTTTCCCACCAATGCACACTTG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878991512 Functional Loss SNV dbSNP153 33..33 33 - - - 46699 RMVar_ID_46699 Human_SNP_ID_146127544 A-to-I Human chr3 - 101576880 101576880 101576880 TTTGCGAGTACTCAACACCAACATCGATGGGCAGCGGAAAATAGCCTTTGCCATCACTGCCATTA TTTGCGAGTACTCAACACCAACATCGATGGGCGGCGGAAAATAGCCTTTGCCATCACTGCCATTA T C AC073861.1 Ensembl:ENSG00000242299 Pseudogene exon GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs879170249 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_584090 46700 RMVar_ID_46700 Human_SNP_ID_146128787 A-to-I Human chr3 + 101581796 101581796 101581796 GAGTTTAACTCCTGTTGCCCAGGCTGCAGTGCAATGGTGCGATCTTGGCTCACTGCAACCTCTGA GAGTTTAACTCCTGTTGCCCAGGCTGCAGTGCGATGGTGCGATCTTGGCTCACTGCAACCTCTGA A G PCNP Ensembl:ENSG00000081154 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1487167625 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48579,RMVar_hsa_circ_22748,RMVar_hsa_circ_95215,RMVar_hsa_circ_220064,RMVar_hsa_circ_96179,RMVar_hsa_circ_310017,RMVar_hsa_circ_114287,RMVar_hsa_circ_220066,RMVar_hsa_circ_108674,RMVar_hsa_circ_220067,RMVar_hsa_circ_220068,RMVar_hsa_circ_220069 46701 RMVar_ID_46701 Human_SNP_ID_146129085 A-to-I Human chr3 + 101583070 101583070 101583070 AGTGGTGAGGCCAGGTGCAGTGGCTCATGCCTATAATTCCAGCACTTTGGGAGGCTGAGGCAGGA AGTGGTGAGGCCAGGTGCAGTGGCTCATGCCTGTAATTCCAGCACTTTGGGAGGCTGAGGCAGGA A G PCNP Ensembl:ENSG00000081154 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs976577621 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25685207 RMVar_hsa_circ_48579,RMVar_hsa_circ_22748,RMVar_hsa_circ_95215,RMVar_hsa_circ_220064,RMVar_hsa_circ_96179,RMVar_hsa_circ_310017,RMVar_hsa_circ_114287,RMVar_hsa_circ_220066,RMVar_hsa_circ_108674,RMVar_hsa_circ_220067,RMVar_hsa_circ_220068 46702 RMVar_ID_46702 Human_SNP_ID_146129146 A-to-I Human chr3 + 101583274 101583274 101583274 AGCCAGGAGTTCGAGACCAGCCTGGCCAACATAGCAAAACTCCATCTCTACTGAAAAATACAAAA AGCCAGGAGTTCGAGACCAGCCTGGCCAACATTGCAAAACTCCATCTCTACTGAAAAATACAAAA A T PCNP Ensembl:ENSG00000081154 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs961089365 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48579,RMVar_hsa_circ_22748,RMVar_hsa_circ_95215,RMVar_hsa_circ_220064,RMVar_hsa_circ_96179,RMVar_hsa_circ_310017,RMVar_hsa_circ_114287,RMVar_hsa_circ_220066,RMVar_hsa_circ_108674,RMVar_hsa_circ_220067,RMVar_hsa_circ_220068 46703 RMVar_ID_46703 Human_SNP_ID_146129160 A-to-I Human chr3 + 101583333 101583333 101583333 ACAAAAAATTAGCCATGGTGGCACACACCTGCAATCCCAGTTACTTGGGAGGCTGAGGCAGGAGA ACAAAAAATTAGCCATGGTGGCACACACCTGCCATCCCAGTTACTTGGGAGGCTGAGGCAGGAGA A C PCNP Ensembl:ENSG00000081154 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946626441 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48579,RMVar_hsa_circ_22748,RMVar_hsa_circ_95215,RMVar_hsa_circ_220064,RMVar_hsa_circ_96179,RMVar_hsa_circ_310017,RMVar_hsa_circ_114287,RMVar_hsa_circ_220066,RMVar_hsa_circ_108674,RMVar_hsa_circ_220067,RMVar_hsa_circ_220068 46704 RMVar_ID_46704 Human_SNP_ID_146129195 A-to-I Human chr3 + 101583493 101583493 101583493 AACAAATGAGCCGGGCATGGCAGGGTGTGCCTATAGTCCCACCTACTTGAGAGGCTGAGGTGGGA AACAAATGAGCCGGGCATGGCAGGGTGTGCCTGTAGTCCCACCTACTTGAGAGGCTGAGGTGGGA A G PCNP Ensembl:ENSG00000081154 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs895453316 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14550546 RMVar_hsa_circ_48579,RMVar_hsa_circ_22748,RMVar_hsa_circ_95215,RMVar_hsa_circ_220064,RMVar_hsa_circ_96179,RMVar_hsa_circ_310017,RMVar_hsa_circ_114287,RMVar_hsa_circ_220066,RMVar_hsa_circ_108674,RMVar_hsa_circ_220067,RMVar_hsa_circ_220068 46705 RMVar_ID_46705 Human_SNP_ID_146129263 A-to-I Human chr3 + 101583701 101583701 101583701 ACAGAGACTCACTCTGTCACCCAGGCTGGAGTACAAAGGTGTGATCTTGGCTCACTGCAACCTCT ACAGAGACTCACTCTGTCACCCAGGCTGGAGTCCAAAGGTGTGATCTTGGCTCACTGCAACCTCT A C PCNP Ensembl:ENSG00000081154 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs13087565 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7098451 RMVar_hsa_circ_48579,RMVar_hsa_circ_22748,RMVar_hsa_circ_95215,RMVar_hsa_circ_220064,RMVar_hsa_circ_96179,RMVar_hsa_circ_310017,RMVar_hsa_circ_114287,RMVar_hsa_circ_220066,RMVar_hsa_circ_108674,RMVar_hsa_circ_220067,RMVar_hsa_circ_220068 46706 RMVar_ID_46706 Human_SNP_ID_146129264 A-to-I Human chr3 + 101583701 101583701 101583701 ACAGAGACTCACTCTGTCACCCAGGCTGGAGTACAAAGGTGTGATCTTGGCTCACTGCAACCTCT ACAGAGACTCACTCTGTCACCCAGGCTGGAGTGCAAAGGTGTGATCTTGGCTCACTGCAACCTCT A G PCNP Ensembl:ENSG00000081154 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs13087565 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7098451 RMVar_hsa_circ_48579,RMVar_hsa_circ_22748,RMVar_hsa_circ_95215,RMVar_hsa_circ_220064,RMVar_hsa_circ_96179,RMVar_hsa_circ_310017,RMVar_hsa_circ_114287,RMVar_hsa_circ_220066,RMVar_hsa_circ_108674,RMVar_hsa_circ_220067,RMVar_hsa_circ_220068 46707 RMVar_ID_46707 Human_SNP_ID_146129283 A-to-I Human chr3 + 101583777 101583777 101583777 TCAACCAATTCTCCTGCCTCAGCCTCCTGAGTAGCTGAGATTACAGGTGTGCATCACCACCATAT TCAACCAATTCTCCTGCCTCAGCCTCCTGAGTTGCTGAGATTACAGGTGTGCATCACCACCATAT A T PCNP Ensembl:ENSG00000081154 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1242495878 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48579,RMVar_hsa_circ_22748,RMVar_hsa_circ_95215,RMVar_hsa_circ_220064,RMVar_hsa_circ_96179,RMVar_hsa_circ_310017,RMVar_hsa_circ_114287,RMVar_hsa_circ_220066,RMVar_hsa_circ_108674,RMVar_hsa_circ_220067,RMVar_hsa_circ_220068 46708 RMVar_ID_46708 Human_SNP_ID_146129287 A-to-I Human chr3 + 101583787 101583787 101583787 CTCCTGCCTCAGCCTCCTGAGTAGCTGAGATTACAGGTGTGCATCACCACCATATCCAGCTAATT CTCCTGCCTCAGCCTCCTGAGTAGCTGAGATTGCAGGTGTGCATCACCACCATATCCAGCTAATT A G PCNP Ensembl:ENSG00000081154 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1430607404 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48579,RMVar_hsa_circ_22748,RMVar_hsa_circ_95215,RMVar_hsa_circ_220064,RMVar_hsa_circ_96179,RMVar_hsa_circ_310017,RMVar_hsa_circ_114287,RMVar_hsa_circ_220066,RMVar_hsa_circ_108674,RMVar_hsa_circ_220067,RMVar_hsa_circ_220068 46709 RMVar_ID_46709 Human_SNP_ID_146129333 A-to-I Human chr3 + 101583916 101583916 101583916 GAACTCCTGACCTCAAGTGATCCACTTGCCTTAGCCTCCCAAAGTGCTGGGATTACAAGCATGAG GAACTCCTGACCTCAAGTGATCCACTTGCCTTGGCCTCCCAAAGTGCTGGGATTACAAGCATGAG A G PCNP Ensembl:ENSG00000081154 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs935837570 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48579,RMVar_hsa_circ_22748,RMVar_hsa_circ_95215,RMVar_hsa_circ_220064,RMVar_hsa_circ_96179,RMVar_hsa_circ_310017,RMVar_hsa_circ_114287,RMVar_hsa_circ_220066,RMVar_hsa_circ_108674,RMVar_hsa_circ_220067,RMVar_hsa_circ_220068 46710 RMVar_ID_46710 Human_SNP_ID_146129468 A-to-I Human chr3 + 101584596 101584592 101584596 TTTTTTTTATTTTTATTTTTTGAGACAGTCTCACTCTGTTACCCAGGCTGGAATGCAGTGGCGTG TTTTTTTTATTTTTATTTTTTGAGACAGT____CTCTGTTACCCAGGCTGGAATGCAGTGGCGTG TCTCA T PCNP Ensembl:ENSG00000081154 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1190230721 Functional Loss DEL dbSNP153 30..33 33 - - - RMVar_hsa_circ_48579,RMVar_hsa_circ_22748,RMVar_hsa_circ_95215,RMVar_hsa_circ_220064,RMVar_hsa_circ_96179,RMVar_hsa_circ_310017,RMVar_hsa_circ_114287,RMVar_hsa_circ_220066,RMVar_hsa_circ_108674,RMVar_hsa_circ_220067,RMVar_hsa_circ_220068 46711 RMVar_ID_46711 Human_SNP_ID_146129469 A-to-I Human chr3 + 101584596 101584596 101584596 TTTTTTTTATTTTTATTTTTTGAGACAGTCTCACTCTGTTACCCAGGCTGGAATGCAGTGGCGTG TTTTTTTTATTTTTATTTTTTGAGACAGTCTCGCTCTGTTACCCAGGCTGGAATGCAGTGGCGTG A G PCNP Ensembl:ENSG00000081154 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs912954126 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48579,RMVar_hsa_circ_22748,RMVar_hsa_circ_95215,RMVar_hsa_circ_220064,RMVar_hsa_circ_96179,RMVar_hsa_circ_310017,RMVar_hsa_circ_114287,RMVar_hsa_circ_220066,RMVar_hsa_circ_108674,RMVar_hsa_circ_220067,RMVar_hsa_circ_220068 46712 RMVar_ID_46712 Human_SNP_ID_146129492 A-to-I Human chr3 + 101584698 101584698 101584698 GCGATTCTCCTGCCTCAGCCTCCCAAGTAACTAGGATTACAGGCACTCACCACCACACCTGGCTG GCGATTCTCCTGCCTCAGCCTCCCAAGTAACTGGGATTACAGGCACTCACCACCACACCTGGCTG A G PCNP Ensembl:ENSG00000081154 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs564396956 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48579,RMVar_hsa_circ_22748,RMVar_hsa_circ_95215,RMVar_hsa_circ_220064,RMVar_hsa_circ_96179,RMVar_hsa_circ_310017,RMVar_hsa_circ_114287,RMVar_hsa_circ_220066,RMVar_hsa_circ_108674,RMVar_hsa_circ_220067,RMVar_hsa_circ_220068 46713 RMVar_ID_46713 Human_SNP_ID_146129564 A-to-I Human chr3 + 101584919 101584919 101584919 CCAGCTATTCAGGACGCCAAGTCATGAGAATCATTTGAACCCAGGAGGCATAGGCTGCAATGAGC CCAGCTATTCAGGACGCCAAGTCATGAGAATCTTTTGAACCCAGGAGGCATAGGCTGCAATGAGC A T PCNP Ensembl:ENSG00000081154 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1335377213 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14550609 RMVar_hsa_circ_48579,RMVar_hsa_circ_22748,RMVar_hsa_circ_95215,RMVar_hsa_circ_220064,RMVar_hsa_circ_96179,RMVar_hsa_circ_310017,RMVar_hsa_circ_114287,RMVar_hsa_circ_220066,RMVar_hsa_circ_108674,RMVar_hsa_circ_220067,RMVar_hsa_circ_220068 46714 RMVar_ID_46714 Human_SNP_ID_146129570 A-to-I Human chr3 + 101584959 101584959 101584959 CCAGGAGGCATAGGCTGCAATGAGCCAAGATTATGCCGCTGCACTCCAGCCTGGGCGACAGAGCA CCAGGAGGCATAGGCTGCAATGAGCCAAGATTGTGCCGCTGCACTCCAGCCTGGGCGACAGAGCA A G PCNP Ensembl:ENSG00000081154 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1389683031 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14550615,Human_RBP_ID_25765410 RMVar_hsa_circ_48579,RMVar_hsa_circ_22748,RMVar_hsa_circ_95215,RMVar_hsa_circ_220064,RMVar_hsa_circ_96179,RMVar_hsa_circ_310017,RMVar_hsa_circ_114287,RMVar_hsa_circ_220066,RMVar_hsa_circ_108674,RMVar_hsa_circ_220067,RMVar_hsa_circ_220068 46715 RMVar_ID_46715 Human_SNP_ID_146129583 A-to-I Human chr3 + 101584991 101584991 101584991 ATGCCGCTGCACTCCAGCCTGGGCGACAGAGCAAGACTCTGTTCTCAAAAAGAAAAACAAAAAAC ATGCCGCTGCACTCCAGCCTGGGCGACAGAGCGAGACTCTGTTCTCAAAAAGAAAAACAAAAAAC A G PCNP Ensembl:ENSG00000081154 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs775815649 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48579,RMVar_hsa_circ_22748,RMVar_hsa_circ_95215,RMVar_hsa_circ_220064,RMVar_hsa_circ_96179,RMVar_hsa_circ_310017,RMVar_hsa_circ_114287,RMVar_hsa_circ_220066,RMVar_hsa_circ_108674,RMVar_hsa_circ_220067,RMVar_hsa_circ_220068 46716 RMVar_ID_46716 Human_SNP_ID_146130257 A-to-I Human chr3 + 101587113 101587113 101587113 TCTCTACTAAAAATACAATATTAGCCGGGCGTAGTGGTGCATGCGTGTAATCCCAGCTACTCAGG TCTCTACTAAAAATACAATATTAGCCGGGCGTGGTGGTGCATGCGTGTAATCCCAGCTACTCAGG A G PCNP Ensembl:ENSG00000081154 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1138747 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95215,RMVar_hsa_circ_220064,RMVar_hsa_circ_96179,RMVar_hsa_circ_114287,RMVar_hsa_circ_220066,RMVar_hsa_circ_108674,RMVar_hsa_circ_220067,RMVar_hsa_circ_220068,RMVar_hsa_circ_288409,RMVar_hsa_circ_220071 46717 RMVar_ID_46717 Human_SNP_ID_146130893 A-to-I Human chr3 + 101589584 101589584 101589584 AGGCACGCGCCACCACACCTGGCCAATTTTTTATACTTTTGGTAGAGACGGGGTTTCACCATGTT AGGCACGCGCCACCACACCTGGCCAATTTTTTGTACTTTTGGTAGAGACGGGGTTTCACCATGTT A G PCNP Ensembl:ENSG00000081154 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1436729232 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95215,RMVar_hsa_circ_220064,RMVar_hsa_circ_96179,RMVar_hsa_circ_114287,RMVar_hsa_circ_220066,RMVar_hsa_circ_108674,RMVar_hsa_circ_220067,RMVar_hsa_circ_220068,RMVar_hsa_circ_288409,RMVar_hsa_circ_220071 46718 RMVar_ID_46718 Human_SNP_ID_146147593 A-to-I Human chr3 - 101656899 101656899 101656899 GAACTCCTGACCTCAAATGATCCGCCCGTCTCAGCCTCCCAAAGTGCTGGGATTACCAGCATGAA GAACTCCTGACCTCAAATGATCCGCCCGTCTCGGCCTCCCAAAGTGCTGGGATTACCAGCATGAA T C ZBTB11 Ensembl:ENSG00000066422 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1194487515 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_675,RMVar_hsa_circ_118737,RMVar_hsa_circ_127750,RMVar_hsa_circ_109060,RMVar_hsa_circ_64233,RMVar_hsa_circ_220073,RMVar_hsa_circ_220075,RMVar_hsa_circ_220074,RMVar_hsa_circ_316577,RMVar_hsa_circ_378713,RMVar_hsa_circ_73654,RMVar_hsa_circ_82119,RMVar_hsa_circ_220078,RMVar_hsa_circ_220079,RMVar_hsa_circ_273741,RMVar_hsa_circ_373472,RMVar_hsa_circ_107565,RMVar_hsa_circ_220080,RMVar_hsa_circ_220082,RMVar_hsa_circ_220083,RMVar_hsa_circ_220081,RMVar_hsa_circ_272651,RMVar_hsa_circ_313942,RMVar_hsa_circ_75123,RMVar_hsa_circ_220085,RMVar_hsa_circ_220086 46719 RMVar_ID_46719 Human_SNP_ID_146150420 A-to-I Human chr3 - 101666862 101666862 101666862 CCTGTAGTCGCACCTACTCCGGAGGCTGAGACAGGAGAATTGCTTGAACCTGGGAGTTGGGAGGT CCTGTAGTCGCACCTACTCCGGAGGCTGAGACGGGAGAATTGCTTGAACCTGGGAGTTGGGAGGT T C ZBTB11 Ensembl:ENSG00000066422 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs758316566 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_247053,Human_RBP_ID_7098818,Human_RBP_ID_14552089 RMVar_hsa_circ_675,RMVar_hsa_circ_127750,RMVar_hsa_circ_64233,RMVar_hsa_circ_220073,RMVar_hsa_circ_316577,RMVar_hsa_circ_82119,RMVar_hsa_circ_220079,RMVar_hsa_circ_273741,RMVar_hsa_circ_107565,RMVar_hsa_circ_220080,RMVar_hsa_circ_220082,RMVar_hsa_circ_220081,RMVar_hsa_circ_272651,RMVar_hsa_circ_220086,RMVar_hsa_circ_312741,RMVar_hsa_circ_220088,RMVar_hsa_circ_57986,RMVar_hsa_circ_314383,RMVar_hsa_circ_15856,RMVar_hsa_circ_220089 46720 RMVar_ID_46720 Human_SNP_ID_146150867 A-to-I Human chr3 - 101668497 101668497 101668497 GGCCTCCCGTGTAGGTGGGACCACAGGTGCACACCACCTTGTCCAACTAATTTTTTCATTTGTTT GGCCTCCCGTGTAGGTGGGACCACAGGTGCACGCCACCTTGTCCAACTAATTTTTTCATTTGTTT T C ZBTB11 Ensembl:ENSG00000066422 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs779845290 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_675,RMVar_hsa_circ_127750,RMVar_hsa_circ_64233,RMVar_hsa_circ_220073,RMVar_hsa_circ_316577,RMVar_hsa_circ_82119,RMVar_hsa_circ_220079,RMVar_hsa_circ_273741,RMVar_hsa_circ_107565,RMVar_hsa_circ_220080,RMVar_hsa_circ_220082,RMVar_hsa_circ_220081,RMVar_hsa_circ_272651,RMVar_hsa_circ_220086,RMVar_hsa_circ_312741,RMVar_hsa_circ_220088,RMVar_hsa_circ_57986,RMVar_hsa_circ_314383,RMVar_hsa_circ_15856,RMVar_hsa_circ_220089 46721 RMVar_ID_46721 Human_SNP_ID_146150873 A-to-I Human chr3 - 101668517 101668517 101668517 TCAAGCAATTTTCCTGCTTTGGCCTCCCGTGTAGGTGGGACCACAGGTGCACACCACCTTGTCCA TCAAGCAATTTTCCTGCTTTGGCCTCCCGTGTGGGTGGGACCACAGGTGCACACCACCTTGTCCA T C ZBTB11 Ensembl:ENSG00000066422 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335649105 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_675,RMVar_hsa_circ_127750,RMVar_hsa_circ_64233,RMVar_hsa_circ_220073,RMVar_hsa_circ_316577,RMVar_hsa_circ_82119,RMVar_hsa_circ_220079,RMVar_hsa_circ_273741,RMVar_hsa_circ_107565,RMVar_hsa_circ_220080,RMVar_hsa_circ_220082,RMVar_hsa_circ_220081,RMVar_hsa_circ_272651,RMVar_hsa_circ_220086,RMVar_hsa_circ_312741,RMVar_hsa_circ_220088,RMVar_hsa_circ_57986,RMVar_hsa_circ_314383,RMVar_hsa_circ_15856,RMVar_hsa_circ_220089 46722 RMVar_ID_46722 Human_SNP_ID_146150880 A-to-I Human chr3 - 101668542 101668542 101668542 TCATAGGCTCAAGCAACTTTTGGGCTCAAGCAATTTTCCTGCTTTGGCCTCCCGTGTAGGTGGGA TCATAGGCTCAAGCAACTTTTGGGCTCAAGCAGTTTTCCTGCTTTGGCCTCCCGTGTAGGTGGGA T C ZBTB11 Ensembl:ENSG00000066422 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs890650483 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14552140 RMVar_hsa_circ_675,RMVar_hsa_circ_127750,RMVar_hsa_circ_64233,RMVar_hsa_circ_220073,RMVar_hsa_circ_316577,RMVar_hsa_circ_82119,RMVar_hsa_circ_220079,RMVar_hsa_circ_273741,RMVar_hsa_circ_107565,RMVar_hsa_circ_220080,RMVar_hsa_circ_220082,RMVar_hsa_circ_220081,RMVar_hsa_circ_272651,RMVar_hsa_circ_220086,RMVar_hsa_circ_312741,RMVar_hsa_circ_220088,RMVar_hsa_circ_57986,RMVar_hsa_circ_314383,RMVar_hsa_circ_15856,RMVar_hsa_circ_220089 46723 RMVar_ID_46723 Human_SNP_ID_146157615 A-to-I Human chr3 + 101690534 101690534 101690534 TTTTGTATTTTTGGTGGAGATGGGGTTTCACCATGTTGCCTTGGCAGGTCTTGAACTGGACTCAA TTTTGTATTTTTGGTGGAGATGGGGTTTCACCTTGTTGCCTTGGCAGGTCTTGAACTGGACTCAA A T AC084198.4 Ensembl:ENSG00000286699 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1169404321 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14552673 46724 RMVar_ID_46724 Human_SNP_ID_146157676 A-to-I Human chr3 + 101690848 101690848 101690848 GCATATGTTATAGGCCCAACTAAACCTCAGTCAGGCCGTGTGTGGTGGCTTATGCCTGTAATGCC GCATATGTTATAGGCCCAACTAAACCTCAGTCGGGCCGTGTGTGGTGGCTTATGCCTGTAATGCC A G AC084198.4 Ensembl:ENSG00000286699 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1263779715 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7098953 46725 RMVar_ID_46725 Human_SNP_ID_146157771 A-to-I Human chr3 + 101691309 101691309 101691309 TCATCACAAAAAGAATCAGGATAGCTTGGTGTAGTGGCAGGTGCCTATAATCCCAGCTACTCAGG TCATCACAAAAAGAATCAGGATAGCTTGGTGTGGTGGCAGGTGCCTATAATCCCAGCTACTCAGG A G AC084198.4 Ensembl:ENSG00000286699 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1136898 Functional Loss SNV dbSNP153 33..33 33 - - - 46726 RMVar_ID_46726 Human_SNP_ID_146157773 A-to-I Human chr3 + 101691315 101691315 101691315 CAAAAAGAATCAGGATAGCTTGGTGTAGTGGCAGGTGCCTATAATCCCAGCTACTCAGGAGACTG CAAAAAGAATCAGGATAGCTTGGTGTAGTGGCGGGTGCCTATAATCCCAGCTACTCAGGAGACTG A G AC084198.4 Ensembl:ENSG00000286699 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1330400169 Functional Loss SNV dbSNP153 33..33 33 - - - 46727 RMVar_ID_46727 Human_SNP_ID_146157787 A-to-I Human chr3 + 101691365 101691365 101691365 CTACTCAGGAGACTGTGGCAGGAGAATGACTTAAACCAGGGAGTTGGAGGTTGCAGTGAGGTGAG CTACTCAGGAGACTGTGGCAGGAGAATGACTTGAACCAGGGAGTTGGAGGTTGCAGTGAGGTGAG A G AC084198.4 Ensembl:ENSG00000286699 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs3205699 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10058891 46728 RMVar_ID_46728 Human_SNP_ID_146157789 A-to-I Human chr3 + 101691387 101691387 101691387 AGAATGACTTAAACCAGGGAGTTGGAGGTTGCAGTGAGGTGAGGTCACACAACTGCACTCCAGAC AGAATGACTTAAACCAGGGAGTTGGAGGTTGCTGTGAGGTGAGGTCACACAACTGCACTCCAGAC A T AC084198.4 Ensembl:ENSG00000286699 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1002750458 Functional Loss SNV dbSNP153 33..33 33 - - - 46729 RMVar_ID_46729 Human_SNP_ID_146167887 A-to-I Human chr3 + 101729198 101729189 101729198 AAGCCCCATCTCTACTAAAAATACCAAAAATTAGTGGGGCATAGTGGTGCGAGCCTGTAGTCCCA AAGCCCCATCTCTACTAAAAATAC_________GTGGGGCATAGTGGTGCGAGCCTGTAGTCCCA CCAAAAATTA C CEP97 Ensembl:ENSG00000182504 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1286518378 Functional Loss DEL dbSNP153 25..33 33 - - - RMVar_hsa_circ_107810,RMVar_hsa_circ_22728,RMVar_hsa_circ_310826,RMVar_hsa_circ_220101,RMVar_hsa_circ_9528,RMVar_hsa_circ_220102,RMVar_hsa_circ_296697,RMVar_hsa_circ_220103 46730 RMVar_ID_46730 Human_SNP_ID_146167888 A-to-I Human chr3 + 101729198 101729198 101729198 AAGCCCCATCTCTACTAAAAATACCAAAAATTAGTGGGGCATAGTGGTGCGAGCCTGTAGTCCCA AAGCCCCATCTCTACTAAAAATACCAAAAATTGGTGGGGCATAGTGGTGCGAGCCTGTAGTCCCA A G CEP97 Ensembl:ENSG00000182504 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs902542619 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107810,RMVar_hsa_circ_22728,RMVar_hsa_circ_310826,RMVar_hsa_circ_220101,RMVar_hsa_circ_9528,RMVar_hsa_circ_220102,RMVar_hsa_circ_296697,RMVar_hsa_circ_220103 46731 RMVar_ID_46731 Human_SNP_ID_146171361 A-to-I Human chr3 + 101743419 101743418 101743420 CTAGAAAAAATATATATATATTTTTTGAAGACAGAGTGTTGCTCTGTTTCCCAGGCTAGAGTGCA CTAGAAAAAATATATATATATTTTTTGAAGAC__AGTGTTGCTCTGTTTCCCAGGCTAGAGTGCA CAG C CEP97 Ensembl:ENSG00000182504 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202626515 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_1343,RMVar_hsa_circ_22728,RMVar_hsa_circ_9528,RMVar_hsa_circ_293018,RMVar_hsa_circ_220105 46732 RMVar_ID_46732 Human_SNP_ID_146177516 A-to-I Human chr3 + 101766954 101766954 101766954 ATGGTACGTGGCATTTGTTGTTATTGTTTTTTAAAGAGATGGAGGCTGGCTCTGTTGGTGCGGTG ATGGTACGTGGCATTTGTTGTTATTGTTTTTTGAAGAGATGGAGGCTGGCTCTGTTGGTGCGGTG A G CEP97 Ensembl:ENSG00000182504 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1255717341 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_584348,Human_RBP_ID_1030157,Human_RBP_ID_3680275,Human_RBP_ID_4715459,Human_RBP_ID_7099084,Human_RBP_ID_8866436,Human_RBP_ID_14553325,Human_RBP_ID_18330825,Human_RBP_ID_22396406,Human_RBP_ID_27709684 46733 RMVar_ID_46733 Human_SNP_ID_146177819 A-to-I Human chr3 + 101768574 101768574 101768574 TTTTAGAAAAGAGACCTGGCGTGGTGGTTGACAACTGTAATCCCAGTGCTTTGGGAGGCTGAGGC TTTTAGAAAAGAGACCTGGCGTGGTGGTTGACTACTGTAATCCCAGTGCTTTGGGAGGCTGAGGC A T CEP97 Ensembl:ENSG00000182504 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,31158229,31158229,32596459 RNA-Seq:(High) rs1443916310 Functional Loss SNV dbSNP153 33..33 33 - - - 46734 RMVar_ID_46734 Human_SNP_ID_146177828 A-to-I Human chr3 + 101768634 101768634 101768634 GAGGCCAGAGGATCACTTGAGGCCAGGAGTTCAAGACCAGCCTGGACAACATAGCAAGACCCCCC GAGGCCAGAGGATCACTTGAGGCCAGGAGTTCCAGACCAGCCTGGACAACATAGCAAGACCCCCC A C CEP97 Ensembl:ENSG00000182504 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs760746114 Functional Loss SNV dbSNP153 33..33 33 - - - 46735 RMVar_ID_46735 Human_SNP_ID_146191064 A-to-I Human chr3 + 101823506 101823506 101823506 TGCAGAATTAAAGAGTCATGGCAGGGTGTGGTAGCTCAAGCCTGTAATCCCAGCACTTTGGGAGG TGCAGAATTAAAGAGTCATGGCAGGGTGTGGTGGCTCAAGCCTGTAATCCCAGCACTTTGGGAGG A G NXPE3 Ensembl:ENSG00000144815 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11548331 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_220115,RMVar_hsa_circ_266658 46736 RMVar_ID_46736 Human_SNP_ID_146191097 A-to-I Human chr3 + 101823666 101823666 101823666 GTGGGCCGACAGTCCCAGCTACTAGGGAGGCTAAGGCAGGGTGATTGATTGAGCCCAGTAGTTTG GTGGGCCGACAGTCCCAGCTACTAGGGAGGCTGAGGCAGGGTGATTGATTGAGCCCAGTAGTTTG A G NXPE3 Ensembl:ENSG00000144815 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,31158229,31158229 RNA-Seq:(High) rs1426696328 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_220115,RMVar_hsa_circ_266658 46737 RMVar_ID_46737 Human_SNP_ID_146191317 A-to-I Human chr3 + 101824608 101824608 101824608 GGGACTACAGGTATGTACCACCATGCCCAGCTAATTTTTGTATCTTTTTGTAGAGACTACATTTT GGGACTACAGGTATGTACCACCATGCCCAGCTGATTTTTGTATCTTTTTGTAGAGACTACATTTT A G NXPE3 Ensembl:ENSG00000144815 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs932926203 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_220115,RMVar_hsa_circ_266658 46738 RMVar_ID_46738 Human_SNP_ID_146798187 A-to-I Human chr3 - 104160706 104160704 104160707 TGTGGTTAGGATTCGGCGCTCTCACCGCCACGACCCGGGTTCAATTCCCGGTCAGGGAACCAAGA TGTGGTTAGGATTCGGCGCTCTCACCGCCAC___CCGGGTTCAATTCCCGGTCAGGGAACCAAGA GGTC G tRNA-Glu-CTC-12-1 RNACentral:URS000074CBFD tRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1252549594 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_270484,Human_RBP_ID_5209795,Human_RBP_ID_8265582,Human_RBP_ID_17667889,Human_RBP_ID_23134623,Human_RBP_ID_23312192 46739 RMVar_ID_46739 Human_SNP_ID_249138527 A-to-I Human chr5 + 122027184 122027184 122027184 CCATCTAAAAAAAAAAATGTTTTTTTTAAGACAGGATCTCATTCTGTTGCCCAGACTAGAGTACA CCATCTAAAAAAAAAAATGTTTTTTTTAAGACGGGATCTCATTCTGTTGCCCAGACTAGAGTACA A G SRFBP1 Ensembl:ENSG00000151304 Protein coding 3'UTR GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs1342975541 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1985153,Human_RBP_ID_22404137,Human_RBP_ID_27330507 RMVar_hsa_circ_233992 46740 RMVar_ID_46740 Human_SNP_ID_249138535 A-to-I Human chr5 + 122027214 122027214 122027214 ACAGGATCTCATTCTGTTGCCCAGACTAGAGTACAATATTGCAATCACAGCTCACTGCAGCCTCA ACAGGATCTCATTCTGTTGCCCAGACTAGAGTCCAATATTGCAATCACAGCTCACTGCAGCCTCA A C SRFBP1 Ensembl:ENSG00000151304 Protein coding 3'UTR GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1182839726 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_629651,Human_RBP_ID_1985153 RMVar_hsa_circ_233992 46741 RMVar_ID_46741 Human_SNP_ID_249138543 A-to-I Human chr5 + 122027246 122027246 122027246 ACAATATTGCAATCACAGCTCACTGCAGCCTCAAACTCCTGGGCTCAAGTGATCCTCCCACCTCT ACAATATTGCAATCACAGCTCACTGCAGCCTCGAACTCCTGGGCTCAAGTGATCCTCCCACCTCT A G SRFBP1 Ensembl:ENSG00000151304 Protein coding 3'UTR GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1028780383 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_233992 46742 RMVar_ID_46742 Human_SNP_ID_249138822 A-to-I Human chr5 + 122028348 122028348 122028348 GATAACTCAGCCGGGCGTGGTGACTCATGCCTATAATCCCAGCACTTTGGGAGGCTGAGGCGGGT GATAACTCAGCCGGGCGTGGTGACTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGT A G SRFBP1 Ensembl:ENSG00000151304 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs375856994 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15275314,Human_RBP_ID_25847661 RMVar_hsa_circ_233992 46743 RMVar_ID_46743 Human_SNP_ID_249138831 A-to-I Human chr5 + 122028395 122028394 122028395 TGGGAGGCTGAGGCGGGTAGATCGCTAGAGGCAAGGAGTTCAAAACCAGCCTGGGCAACATGGTG TGGGAGGCTGAGGCGGGTAGATCGCTAGAGGC_AGGAGTTCAAAACCAGCCTGGGCAACATGGTG CA C SRFBP1 Ensembl:ENSG00000151304 Protein coding 3'UTR GSE100210;GSE107867 HepG2 cell line;ASD brains,frontal_cortex - 29129909,30559470 RNA-Seq:(High) rs948924704 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_233992 46744 RMVar_ID_46744 Human_SNP_ID_249138851 A-to-I Human chr5 + 122028452 122028452 122028452 ACATGGTGAAACCCTGTCTCTACTAAAAATACAGAAAATTATCCAGGCGTGGTGGCCGGCATCTG ACATGGTGAAACCCTGTCTCTACTAAAAATACGGAAAATTATCCAGGCGTGGTGGCCGGCATCTG A G SRFBP1 Ensembl:ENSG00000151304 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs550175882 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_233992 46745 RMVar_ID_46745 Human_SNP_ID_249138860 A-to-I Human chr5 + 122028496 122028496 122028496 AGGCGTGGTGGCCGGCATCTGTAATTCCAGCTACTCAGAAGGCTGAGGCATAAGAATTGCTTGAA AGGCGTGGTGGCCGGCATCTGTAATTCCAGCTGCTCAGAAGGCTGAGGCATAAGAATTGCTTGAA A G SRFBP1 Ensembl:ENSG00000151304 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1046444064 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_233992 46746 RMVar_ID_46746 Human_SNP_ID_249139618 A-to-I Human chr5 + 122031401 122031401 122031401 AGAATGGTCCATGCACTGATGGGGAAAAAAGCAATAGAAATTCCCTGAGGAAGCCCAGACTTCAC AGAATGGTCCATGCACTGATGGGGAAAAAAGCGATAGAAATTCCCTGAGGAAGCCCAGACTTCAC A G SRFBP1 Ensembl:ENSG00000151304 Protein coding intron GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line - 24183664,31158229 RNA-Seq:(High) rs903216443 Functional Loss SNV dbSNP153 33..33 33 - - - 46747 RMVar_ID_46747 Human_SNP_ID_249141306 A-to-I Human chr5 + 122037100 122037100 122037100 TTGTATTTTTGGTAGAAACAGGGTTTCTCTATATTGATCAGGCTGGTCTCCAACTCCCGACCTCA TTGTATTTTTGGTAGAAACAGGGTTTCTCTATGTTGATCAGGCTGGTCTCCAACTCCCGACCTCA A G SRFBP1 Ensembl:ENSG00000151304 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984307357 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15275557 46748 RMVar_ID_46748 Human_SNP_ID_249338555 A-to-I Human chr5 + 122792486 122792486 122792486 GGGTGTGGTGGCGGGTGCCTGTGGTCCCGGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAA GGGTGTGGTGGCGGGTGCCTGTGGTCCCGGCTGCTTGGGAGGCTGAGGCAGGAGAATCGCTTGAA A G SNX2 Ensembl:ENSG00000205302 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs988004441 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_168263 46749 RMVar_ID_46749 Human_SNP_ID_249341530 A-to-I Human chr5 + 122803955 122803955 122803955 GAGGTTAGGAGTTCAAGACCAGCCTAGCCAACATGGTGAAACCCCTGTCTCTAGTAAAATACAAA GAGGTTAGGAGTTCAAGACCAGCCTAGCCAACGTGGTGAAACCCCTGTCTCTAGTAAAATACAAA A G SNX2 Ensembl:ENSG00000205302 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs769527271 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_169,RMVar_hsa_circ_300931,RMVar_hsa_circ_338125,RMVar_hsa_circ_283304,RMVar_hsa_circ_234007,RMVar_hsa_circ_47807,RMVar_hsa_circ_324859,RMVar_hsa_circ_234006,RMVar_hsa_circ_351169,RMVar_hsa_circ_42462,RMVar_hsa_circ_234014,RMVar_hsa_circ_313571,RMVar_hsa_circ_359959,RMVar_hsa_circ_345749,RMVar_hsa_circ_234013,RMVar_hsa_circ_15751 46750 RMVar_ID_46750 Human_SNP_ID_249360517 A-to-I Human chr5 + 122878885 122878885 122878885 GTAATCCCCACTACTCAAGAGGCTGAGGAAGGAAGATCGTTTGAGCCCAGGAGGTCAAGGCTGCA GTAATCCCCACTACTCAAGAGGCTGAGGAAGGGAGATCGTTTGAGCCCAGGAGGTCAAGGCTGCA A G SNX24 Ensembl:ENSG00000064652 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs923494242 Functional Loss SNV dbSNP153 33..33 33 - - - 46751 RMVar_ID_46751 Human_SNP_ID_249361275 A-to-I Human chr5 + 122882090 122882090 122882090 CTCTCACCTTGACCTCTGGAGTAGCTAGGAATATAGGTGCTTGCCACCATGCCCAACTAATTTTT CTCTCACCTTGACCTCTGGAGTAGCTAGGAATGTAGGTGCTTGCCACCATGCCCAACTAATTTTT A G SNX24 Ensembl:ENSG00000064652 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs558818323 Functional Loss SNV dbSNP153 33..33 33 - - - 46752 RMVar_ID_46752 Human_SNP_ID_249493127 A-to-I Human chr5 - 123406633 123406633 123406633 GAGTTTTTATTTCTCCTTCACTTTTGAAGGATAATTTTACTGGGCACAGAATTCTAGGGTGGTGG GAGTTTTTATTTCTCCTTCACTTTTGAAGGATGATTTTACTGGGCACAGAATTCTAGGGTGGTGG T C CEP120 Ensembl:ENSG00000168944 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs912474851 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15278274,Human_RBP_ID_25848203 RMVar_hsa_circ_19223,RMVar_hsa_circ_36351,RMVar_hsa_circ_62847,RMVar_hsa_circ_234027,RMVar_hsa_circ_234030,RMVar_hsa_circ_75701,RMVar_hsa_circ_26979,RMVar_hsa_circ_71069 46753 RMVar_ID_46753 Human_SNP_ID_249493129 A-to-I Human chr5 - 123406638 123406638 123406638 TCTGAGAGTTTTTATTTCTCCTTCACTTTTGAAGGATAATTTTACTGGGCACAGAATTCTAGGGT TCTGAGAGTTTTTATTTCTCCTTCACTTTTGAGGGATAATTTTACTGGGCACAGAATTCTAGGGT T C CEP120 Ensembl:ENSG00000168944 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1184474710 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15278274 RMVar_hsa_circ_19223,RMVar_hsa_circ_36351,RMVar_hsa_circ_62847,RMVar_hsa_circ_234027,RMVar_hsa_circ_234030,RMVar_hsa_circ_75701,RMVar_hsa_circ_26979,RMVar_hsa_circ_71069 46754 RMVar_ID_46754 Human_SNP_ID_249493135 A-to-I Human chr5 - 123406657 123406656 123406657 TGCCCTCAATTTTTATTTGTCTGAGAGTTTTTATTTCTCCTTCACTTTTGAAGGATAATTTTACT TGCCCTCAATTTTTATTTGTCTGAGAGTTTTT_TTTCTCCTTCACTTTTGAAGGATAATTTTACT AT A CEP120 Ensembl:ENSG00000168944 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1244351546 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_19223,RMVar_hsa_circ_36351,RMVar_hsa_circ_62847,RMVar_hsa_circ_234027,RMVar_hsa_circ_234030,RMVar_hsa_circ_75701,RMVar_hsa_circ_26979,RMVar_hsa_circ_71069 46755 RMVar_ID_46755 Human_SNP_ID_250285496 A-to-I Human chr5 + 126447438 126447438 126447438 TAATCCCAGCACTTTGGGAGGCCAAGGCGGGCAGATCATGAGGTCAGAAGATTGAGACCATCCTC TAATCCCAGCACTTTGGGAGGCCAAGGCGGGCGGATCATGAGGTCAGAAGATTGAGACCATCCTC A G GRAMD2B Ensembl:ENSG00000155324 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs953663159 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18558 46756 RMVar_ID_46756 Human_SNP_ID_250304212 A-to-I Human chr5 + 126526302 126526302 126526302 TATAACATGAGAGGCTTCATAGAAAAAAATGAAAATCCAAAGGACCGTTAGACCTAGGGGCTCAC TATAACATGAGAGGCTTCATAGAAAAAAATGAGAATCCAAAGGACCGTTAGACCTAGGGGCTCAC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs988523713 Functional Loss SNV dbSNP153 33..33 33 - - - 46757 RMVar_ID_46757 Human_SNP_ID_250308523 A-to-I Human chr5 - 126543698 126543698 126543698 TTCTCTGCTCCCCTTCTGCATGGCACCCCTCTACTCCTGCCAGGTTAGAATGGAGCAGAGGCCTT TTCTCTGCTCCCCTTCTGCATGGCACCCCTCTCCTCCTGCCAGGTTAGAATGGAGCAGAGGCCTT T G ALDH7A1 Ensembl:ENSG00000164904 Protein coding intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1410102010 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25849041 RMVar_hsa_circ_265700 46758 RMVar_ID_46758 Human_SNP_ID_250313312 A-to-I Human chr5 - 126561826 126561826 126561826 ATCATGCCCAGCTAGTTTGTTTTAATTTTTGTAGAGACAGGGTCTTGCCATGTTGCCCAGGCTCT ATCATGCCCAGCTAGTTTGTTTTAATTTTTGTGGAGACAGGGTCTTGCCATGTTGCCCAGGCTCT T C ALDH7A1 Ensembl:ENSG00000164904 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1174740271 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23037887 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 46759 RMVar_ID_46759 Human_SNP_ID_250313416 A-to-I Human chr5 - 126562276 126562276 126562276 ATTGCTTGAGCCCAGGAGGTTGAGGCTGCAGTAAGCCATGATCATGCTAGTACACCCCAGCCTGG ATTGCTTGAGCCCAGGAGGTTGAGGCTGCAGTGAGCCATGATCATGCTAGTACACCCCAGCCTGG T C ALDH7A1 Ensembl:ENSG00000164904 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1006155794 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17575452 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 46760 RMVar_ID_46760 Human_SNP_ID_250313734 A-to-I Human chr5 - 126563629 126563629 126563629 AAAAAGAGCTGGGCGTGATGGTGCATGCCTGTAGTCCCAGCTACTTGGGAAGCTGAGACAGGAGA AAAAAGAGCTGGGCGTGATGGTGCATGCCTGTTGTCCCAGCTACTTGGGAAGCTGAGACAGGAGA T A ALDH7A1 Ensembl:ENSG00000164904 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041972630 Functional Loss SNV dbSNP153 33..33 33 - - - 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 46761 RMVar_ID_46761 Human_SNP_ID_250313911 A-to-I Human chr5 - 126564306 126564306 126564306 CCCATCCCTACTAAAATACAAAAAAATTAGCTAGGTGTGGCGGCATGCCCAGCTACTTGGGAGGC CCCATCCCTACTAAAATACAAAAAAATTAGCTGGGTGTGGCGGCATGCCCAGCTACTTGGGAGGC T C ALDH7A1 Ensembl:ENSG00000164904 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs546406731 Functional Loss SNV dbSNP153 33..33 33 - - - 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 46762 RMVar_ID_46762 Human_SNP_ID_250314746 A-to-I Human chr5 - 126567643 126567643 126567643 ATGGTGAAACCCCGTCTCTGCTAAAAATACAAAAAGTAGCCGGGCGTGGTGGCATGTGCCTGTAA ATGGTGAAACCCCGTCTCTGCTAAAAATACAAGAAGTAGCCGGGCGTGGTGGCATGTGCCTGTAA T C ALDH7A1 Ensembl:ENSG00000164904 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1365198014 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25849241 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 46763 RMVar_ID_46763 Human_SNP_ID_250314753 A-to-I Human chr5 - 126567668 126567668 126567668 GGAGCTCAAGACCAGCCTGGGCAAGATGGTGAAACCCCGTCTCTGCTAAAAATACAAAAAGTAGC GGAGCTCAAGACCAGCCTGGGCAAGATGGTGACACCCCGTCTCTGCTAAAAATACAAAAAGTAGC T G ALDH7A1 Ensembl:ENSG00000164904 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1025917712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10177843,Human_RBP_ID_23037906,Human_RBP_ID_25935931 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 46764 RMVar_ID_46764 Human_SNP_ID_250317913 A-to-I Human chr5 - 126579785 126579785 126579785 CAGCTAATTTAAAAATTTTTCTTGTAGAGACGAGGTTGCACTATGTGGCCTAGGCTGGTCTAGAA CAGCTAATTTAAAAATTTTTCTTGTAGAGACGGGGTTGCACTATGTGGCCTAGGCTGGTCTAGAA T C ALDH7A1 Ensembl:ENSG00000164904 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1162979432 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 46765 RMVar_ID_46765 Human_SNP_ID_250318347 A-to-I Human chr5 - 126581539 126581532 126581539 CAGTTCACTGCAGCCTCAACATCCCCGGGATCAGGTGATCCTCCTACCTCAGCTAGGACTGTAGG CAGTTCACTGCAGCCTCAACATCCCCGGGATC_______CCTCCTACCTCAGCTAGGACTGTAGG GATCACCT G ALDH7A1 Ensembl:ENSG00000164904 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432591395 Functional Loss DEL dbSNP153 33..39 33 - - - Human_RBP_ID_15279547 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 46766 RMVar_ID_46766 Human_SNP_ID_250318349 A-to-I Human chr5 - 126581539 126581539 126581539 CAGTTCACTGCAGCCTCAACATCCCCGGGATCAGGTGATCCTCCTACCTCAGCTAGGACTGTAGG CAGTTCACTGCAGCCTCAACATCCCCGGGATCTGGTGATCCTCCTACCTCAGCTAGGACTGTAGG T A ALDH7A1 Ensembl:ENSG00000164904 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs949113689 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15279547 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 46767 RMVar_ID_46767 Human_SNP_ID_250327356 A-to-I Human chr5 + 126613505 126613505 126613505 TGAGACCAGCCTGGGTGACATGGTGAAACCTTATCTCTACCAAAAAAATACAAAAATTAGCTGTA TGAGACCAGCCTGGGTGACATGGTGAAACCTTGTCTCTACCAAAAAAATACAAAAATTAGCTGTA A G PHAX Ensembl:ENSG00000164902 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1315643224 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80867,RMVar_hsa_circ_234089,RMVar_hsa_circ_234086,RMVar_hsa_circ_358394,RMVar_hsa_circ_113766,RMVar_hsa_circ_234090 46768 RMVar_ID_46768 Human_SNP_ID_250328936 A-to-I Human chr5 + 126619201 126619201 126619201 CTCCCACCTTGGCCTCCGAAAGTGCTGGAATTACAGGTGTTAGCCACCTTGCCTGGCCCTCCTTT CTCCCACCTTGGCCTCCGAAAGTGCTGGAATTGCAGGTGTTAGCCACCTTGCCTGGCCCTCCTTT A G PHAX Ensembl:ENSG00000164902 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1431373488 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80867,RMVar_hsa_circ_234086,RMVar_hsa_circ_113766,RMVar_hsa_circ_234090 46769 RMVar_ID_46769 Human_SNP_ID_250330458 A-to-I Human chr5 + 126625341 126625341 126625341 AACATTGGCCAGGCACGGTGGCTCACGCCTGTAATCCCAACACTTTAGGAGACCAAGGCGGGCAG AACATTGGCCAGGCACGGTGGCTCACGCCTGTGATCCCAACACTTTAGGAGACCAAGGCGGGCAG A G PHAX Ensembl:ENSG00000164902 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1138215 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80867,RMVar_hsa_circ_234086,RMVar_hsa_circ_113766,RMVar_hsa_circ_234090 46770 RMVar_ID_46770 Human_SNP_ID_250330462 A-to-I Human chr5 + 126625355 126625355 126625355 ACGGTGGCTCACGCCTGTAATCCCAACACTTTAGGAGACCAAGGCGGGCAGATCACTTGAGGTCA ACGGTGGCTCACGCCTGTAATCCCAACACTTTCGGAGACCAAGGCGGGCAGATCACTTGAGGTCA A C PHAX Ensembl:ENSG00000164902 Protein coding 3'UTR GSE38233;GSE99789 cultured B-cells;esophageal squamous carcinoma cells,EC109 - 24183664,29796672 RNA-Seq:(High) rs879038407 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80867,RMVar_hsa_circ_234086,RMVar_hsa_circ_113766,RMVar_hsa_circ_234090 46771 RMVar_ID_46771 Human_SNP_ID_250330469 A-to-I Human chr5 + 126625387 126625387 126625387 AGGAGACCAAGGCGGGCAGATCACTTGAGGTCAGAAGTTTGAGACCAGCCAGGCCAACATGGTGA AGGAGACCAAGGCGGGCAGATCACTTGAGGTCGGAAGTTTGAGACCAGCCAGGCCAACATGGTGA A G PHAX Ensembl:ENSG00000164902 Protein coding 3'UTR GSE47997;GSE38233;GSE99789;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;cultured B-cells;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BERP35T1 cell line - 23474544,24183664,29796672,31158229 RNA-Seq:(High) rs898481838 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_469242,Human_miRNA_ID_607383,Human_miRNA_ID_2330816,Human_miRNA_ID_2516593,Human_miRNA_ID_2963899 RMVar_hsa_circ_80867,RMVar_hsa_circ_234086,RMVar_hsa_circ_113766,RMVar_hsa_circ_234090 46772 RMVar_ID_46772 Human_SNP_ID_250330486 A-to-I Human chr5 + 126625474 126625474 126625474 CAAAAACTAGCCAGGTGTGGTTCTCCATGCCTATAATCCCGGCTACTCGGGAGGCTGAGGCAGGA CAAAAACTAGCCAGGTGTGGTTCTCCATGCCTGTAATCCCGGCTACTCGGGAGGCTGAGGCAGGA A G PHAX Ensembl:ENSG00000164902 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;ASD brains,cerebellum;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,29129909,30559470,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs1021096243 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_165724,Human_RBP_ID_4848579,Human_RBP_ID_9304655,Human_RBP_ID_18352340 RMVar_hsa_circ_80867,RMVar_hsa_circ_234086,RMVar_hsa_circ_113766,RMVar_hsa_circ_234090 46773 RMVar_ID_46773 Human_SNP_ID_250330570 A-to-I Human chr5 + 126625721 126625718 126625722 CAAGTAACTATTTGTTTTTTGGGGGGTTTTTTAGTTAGAGTCTTGATCTGTCACCCAGGCTGGAG CAAGTAACTATTTGTTTTTTGGGGGGTTTT____TTAGAGTCTTGATCTGTCACCCAGGCTGGAG TTTAG T PHAX Ensembl:ENSG00000164902 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1446561335 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_629985,Human_RBP_ID_7375429,Human_RBP_ID_26520461 RMVar_hsa_circ_80867,RMVar_hsa_circ_234086,RMVar_hsa_circ_113766,RMVar_hsa_circ_234090 46774 RMVar_ID_46774 Human_SNP_ID_250330579 A-to-I Human chr5 + 126625766 126625766 126625766 ATCTGTCACCCAGGCTGGAGTACAGTGGCAGGATCTCAGCTTACTGCAGCTTCCATCTCCCAGGT ATCTGTCACCCAGGCTGGAGTACAGTGGCAGGGTCTCAGCTTACTGCAGCTTCCATCTCCCAGGT A G PHAX Ensembl:ENSG00000164902 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1196124298 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80867,RMVar_hsa_circ_234086,RMVar_hsa_circ_113766,RMVar_hsa_circ_234090 46775 RMVar_ID_46775 Human_SNP_ID_250330580 A-to-I Human chr5 + 126625776 126625776 126625776 CAGGCTGGAGTACAGTGGCAGGATCTCAGCTTACTGCAGCTTCCATCTCCCAGGTTCAAGCGATC CAGGCTGGAGTACAGTGGCAGGATCTCAGCTTGCTGCAGCTTCCATCTCCCAGGTTCAAGCGATC A G PHAX Ensembl:ENSG00000164902 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1138235 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80867,RMVar_hsa_circ_234086,RMVar_hsa_circ_113766,RMVar_hsa_circ_234090 46776 RMVar_ID_46776 Human_SNP_ID_250330610 A-to-I Human chr5 + 126625862 126625862 126625862 AGCTGGGATCACAGGTGTGTACCACCACGCCCAGCTGATTTTTGTATTTTTAGTAAAGACTTTCG AGCTGGGATCACAGGTGTGTACCACCACGCCCCGCTGATTTTTGTATTTTTAGTAAAGACTTTCG A C PHAX Ensembl:ENSG00000164902 Protein coding 3'UTR GSE38233;GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,32596459 RNA-Seq:(High) rs1210484560 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80867,RMVar_hsa_circ_234086,RMVar_hsa_circ_113766,RMVar_hsa_circ_234090 46777 RMVar_ID_46777 Human_SNP_ID_250330626 A-to-I Human chr5 + 126625897 126625897 126625897 TGATTTTTGTATTTTTAGTAAAGACTTTCGCCATGTTGTCCAGGCTGGTCTCGAACTCCTGGCCT TGATTTTTGTATTTTTAGTAAAGACTTTCGCCGTGTTGTCCAGGCTGGTCTCGAACTCCTGGCCT A G PHAX Ensembl:ENSG00000164902 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs963932629 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26520464 RMVar_hsa_circ_80867,RMVar_hsa_circ_234086,RMVar_hsa_circ_113766,RMVar_hsa_circ_234090 46778 RMVar_ID_46778 Human_SNP_ID_250330633 A-to-I Human chr5 + 126625930 126625930 126625930 TGTTGTCCAGGCTGGTCTCGAACTCCTGGCCTAATGATCTGCCCACCTCTGCCTCCCAAAGTGCT TGTTGTCCAGGCTGGTCTCGAACTCCTGGCCTGATGATCTGCCCACCTCTGCCTCCCAAAGTGCT A G PHAX Ensembl:ENSG00000164902 Protein coding 3'UTR GSE38233;GSE100210;GSE107867;GSE107867;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,30559470,30559470,32596459 RNA-Seq:(High) rs1488722098 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4806249,Human_RBP_ID_18037127,Human_RBP_ID_18352343,Human_RBP_ID_25849474 RMVar_hsa_circ_80867,RMVar_hsa_circ_234086,RMVar_hsa_circ_113766,RMVar_hsa_circ_234090 46779 RMVar_ID_46779 Human_SNP_ID_250330638 A-to-I Human chr5 + 126625942 126625942 126625942 TGGTCTCGAACTCCTGGCCTAATGATCTGCCCACCTCTGCCTCCCAAAGTGCTGGGATCACAGGC TGGTCTCGAACTCCTGGCCTAATGATCTGCCCGCCTCTGCCTCCCAAAGTGCTGGGATCACAGGC A G PHAX Ensembl:ENSG00000164902 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1138245 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18037127 RMVar_hsa_circ_80867,RMVar_hsa_circ_234086,RMVar_hsa_circ_113766,RMVar_hsa_circ_234090 46780 RMVar_ID_46780 Human_SNP_ID_250330641 A-to-I Human chr5 + 126625955 126625955 126625955 CTGGCCTAATGATCTGCCCACCTCTGCCTCCCAAAGTGCTGGGATCACAGGCATGAGCCACCGAA CTGGCCTAATGATCTGCCCACCTCTGCCTCCCTAAGTGCTGGGATCACAGGCATGAGCCACCGAA A T PHAX Ensembl:ENSG00000164902 Protein coding 3'UTR GSE38233;GSE107867;GSE107867 cultured B-cells;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;ASD brains,temporal_cortex - 24183664,30559470,30559470 RNA-Seq:(High) rs191804124 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80867,RMVar_hsa_circ_234086,RMVar_hsa_circ_113766,RMVar_hsa_circ_234090 46781 RMVar_ID_46781 Human_SNP_ID_250330642 A-to-I Human chr5 + 126625956 126625956 126625956 TGGCCTAATGATCTGCCCACCTCTGCCTCCCAAAGTGCTGGGATCACAGGCATGAGCCACCGAAC TGGCCTAATGATCTGCCCACCTCTGCCTCCCATAGTGCTGGGATCACAGGCATGAGCCACCGAAC A T PHAX Ensembl:ENSG00000164902 Protein coding 3'UTR GSE107867;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 ASD brains,temporal_cortex;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 30559470,32596459,32596459 RNA-Seq:(High) rs1339120880 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80867,RMVar_hsa_circ_234086,RMVar_hsa_circ_113766,RMVar_hsa_circ_234090 46782 RMVar_ID_46782 Human_SNP_ID_250330685 A-to-I Human chr5 + 126626124 126626124 126626124 TTTTCAAGCTGGGCCTAGTGGCGCACACCTGCAATCCCAACACTTTGGGAGGCCAAGAGAGGAAG TTTTCAAGCTGGGCCTAGTGGCGCACACCTGCGATCCCAACACTTTGGGAGGCCAAGAGAGGAAG A G PHAX Ensembl:ENSG00000164902 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1138207 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80867,RMVar_hsa_circ_234086,RMVar_hsa_circ_113766,RMVar_hsa_circ_234090 46783 RMVar_ID_46783 Human_SNP_ID_250330761 A-to-I Human chr5 + 126626392 126626392 126626392 GAGACAGGTAGATCATTTGAGGTCAGGAGTTCAAAACCAACCTGGTCTACATGGTGAAACCCCAT GAGACAGGTAGATCATTTGAGGTCAGGAGTTCGAAACCAACCTGGTCTACATGGTGAAACCCCAT A G PHAX Ensembl:ENSG00000164902 Protein coding 3'UTR GSE38233;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,32596459 RNA-Seq:(High) rs1038780306 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80867,RMVar_hsa_circ_234086,RMVar_hsa_circ_113766,RMVar_hsa_circ_234090 46784 RMVar_ID_46784 Human_SNP_ID_250330793 A-to-I Human chr5 + 126626477 126626477 126626477 ATACAAAAAATTAGCCGGGCGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGTGGAGGC ATACAAAAAATTAGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGTGGAGGC A G PHAX Ensembl:ENSG00000164902 Protein coding 3'UTR GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs999019059 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80867,RMVar_hsa_circ_234086,RMVar_hsa_circ_113766,RMVar_hsa_circ_234090 46785 RMVar_ID_46785 Human_SNP_ID_250330812 A-to-I Human chr5 + 126626527 126626526 126626528 TTGGGAGGTGGAGGCGGGTGGATCACAAGGTCAAGAGATCGAGACCATCCTGGCCAACATGGTGA TTGGGAGGTGGAGGCGGGTGGATCACAAGGTC__GAGATCGAGACCATCCTGGCCAACATGGTGA CAA C PHAX Ensembl:ENSG00000164902 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs201868659 Functional Loss DEL dbSNP153 33..34 33 - - - Human_miRNA_ID_469243,Human_miRNA_ID_607384,Human_miRNA_ID_1690745,Human_miRNA_ID_1956533 RMVar_hsa_circ_80867,RMVar_hsa_circ_234086,RMVar_hsa_circ_113766,RMVar_hsa_circ_234090 46786 RMVar_ID_46786 Human_SNP_ID_250331405 A-to-I Human chr5 + 126628499 126628499 126628499 TAAAAATTTATCGGCCCGGCATGGTGGCTCATACCTGTAATTCTAACACTGGGAGGCCGAGGCAG TAAAAATTTATCGGCCCGGCATGGTGGCTCATTCCTGTAATTCTAACACTGGGAGGCCGAGGCAG A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1236355335 Functional Loss SNV dbSNP153 33..33 33 - - - 46787 RMVar_ID_46787 Human_SNP_ID_250375701 A-to-I Human chr5 + 126781566 126781566 126781566 TCAAGCGATGCTCTTGACCCAGCCTCCCAAGTAGCTGGGATTACAGGTGTGCACCACCACACCCG TCAAGCGATGCTCTTGACCCAGCCTCCCAAGTCGCTGGGATTACAGGTGTGCACCACCACACCCG A C LMNB1 Ensembl:ENSG00000113368 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs993908464 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77912,RMVar_hsa_circ_111166,RMVar_hsa_circ_234091,RMVar_hsa_circ_234092 46788 RMVar_ID_46788 Human_SNP_ID_250377818 A-to-I Human chr5 + 126788494 126788494 126788494 CCCCGTTTCTACTAAAAATGCAAAAATTAGCCAGGCGTGGTTGCACATGCCTTTAATCTCAACTA CCCCGTTTCTACTAAAAATGCAAAAATTAGCCGGGCGTGGTTGCACATGCCTTTAATCTCAACTA A G LMNB1 Ensembl:ENSG00000113368 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1242432212 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77912,RMVar_hsa_circ_111166,RMVar_hsa_circ_234091,RMVar_hsa_circ_234092 46789 RMVar_ID_46789 Human_SNP_ID_250377829 A-to-I Human chr5 + 126788543 126788543 126788543 CCTTTAATCTCAACTACTGTGGAGGCTGAGGCAGGAGAATCACTTGAACCTGGGAGGCGGAGGTT CCTTTAATCTCAACTACTGTGGAGGCTGAGGCGGGAGAATCACTTGAACCTGGGAGGCGGAGGTT A G LMNB1 Ensembl:ENSG00000113368 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs897817640 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77912,RMVar_hsa_circ_111166,RMVar_hsa_circ_234091,RMVar_hsa_circ_234092 46790 RMVar_ID_46790 Human_SNP_ID_250386198 A-to-I Human chr5 + 126819916 126819916 126819916 CCTGTAATCCCGGCACTTTGGGAGGCCAAGGCAGGCGGATCACATGAGGTCAGGAGTTCAAGACC CCTGTAATCCCGGCACTTTGGGAGGCCAAGGCGGGCGGATCACATGAGGTCAGGAGTTCAAGACC A G LMNB1 Ensembl:ENSG00000113368 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1236504703 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77912,RMVar_hsa_circ_111166,RMVar_hsa_circ_234091,RMVar_hsa_circ_331702,RMVar_hsa_circ_234092,RMVar_hsa_circ_317009,RMVar_hsa_circ_278490,RMVar_hsa_circ_269995,RMVar_hsa_circ_234098,RMVar_hsa_circ_234099,RMVar_hsa_circ_234100,RMVar_hsa_circ_234097,RMVar_hsa_circ_12255,RMVar_hsa_circ_15576,RMVar_hsa_circ_347816,RMVar_hsa_circ_355681,RMVar_hsa_circ_336793,RMVar_hsa_circ_297079,RMVar_hsa_circ_234102,RMVar_hsa_circ_335165,RMVar_hsa_circ_301602,RMVar_hsa_circ_308541,RMVar_hsa_circ_33759 46791 RMVar_ID_46791 Human_SNP_ID_250386261 A-to-I Human chr5 + 126820124 126820123 126820125 AGATTGTGCCATTGCACTCCAGCCTGGGTGACAAGAGTGAAACTCTGTCTCACAAAAAAAAGAAA AGATTGTGCCATTGCACTCCAGCCTGGGTGAC__GAGTGAAACTCTGTCTCACAAAAAAAAGAAA CAA C LMNB1 Ensembl:ENSG00000113368 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1052191742 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_77912,RMVar_hsa_circ_111166,RMVar_hsa_circ_234091,RMVar_hsa_circ_331702,RMVar_hsa_circ_234092,RMVar_hsa_circ_317009,RMVar_hsa_circ_278490,RMVar_hsa_circ_269995,RMVar_hsa_circ_234098,RMVar_hsa_circ_234099,RMVar_hsa_circ_234100,RMVar_hsa_circ_234097,RMVar_hsa_circ_12255,RMVar_hsa_circ_15576,RMVar_hsa_circ_347816,RMVar_hsa_circ_355681,RMVar_hsa_circ_336793,RMVar_hsa_circ_297079,RMVar_hsa_circ_234102,RMVar_hsa_circ_335165,RMVar_hsa_circ_301602,RMVar_hsa_circ_308541,RMVar_hsa_circ_33759 46792 RMVar_ID_46792 Human_SNP_ID_250387994 A-to-I Human chr5 + 126827477 126827477 126827477 GAGGTCAGGAGTTAGAGACCAGCGTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAACACAAG GAGGTCAGGAGTTAGAGACCAGCGTGGCCAACGTGGTGAAACCCCGTCTCTACTAAAAACACAAG A G LMNB1 Ensembl:ENSG00000113368 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs955199511 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269995,RMVar_hsa_circ_234100,RMVar_hsa_circ_347816,RMVar_hsa_circ_301602 46793 RMVar_ID_46793 Human_SNP_ID_250388308 A-to-I Human chr5 + 126828735 126828735 126828735 CAGGTGCGTGCCAACACACCTGGCTAATTTTTATATTTTTAGTAGAGATGGGGTTTTACCATATT CAGGTGCGTGCCAACACACCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTTACCATATT A G LMNB1 Ensembl:ENSG00000113368 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs772420490 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269995,RMVar_hsa_circ_234100,RMVar_hsa_circ_347816,RMVar_hsa_circ_301602 46794 RMVar_ID_46794 Human_SNP_ID_250388309 A-to-I Human chr5 + 126828735 126828735 126828735 CAGGTGCGTGCCAACACACCTGGCTAATTTTTATATTTTTAGTAGAGATGGGGTTTTACCATATT CAGGTGCGTGCCAACACACCTGGCTAATTTTTTTATTTTTAGTAGAGATGGGGTTTTACCATATT A T LMNB1 Ensembl:ENSG00000113368 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs772420490 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269995,RMVar_hsa_circ_234100,RMVar_hsa_circ_347816,RMVar_hsa_circ_301602 46795 RMVar_ID_46795 Human_SNP_ID_250388398 A-to-I Human chr5 + 126829047 126829047 126829047 AAGACCATATTTGTCAGTAGGGACCAGACCACATTAGGAACAATCTATAAACAATCCCCGCCATA AAGACCATATTTGTCAGTAGGGACCAGACCACGTTAGGAACAATCTATAAACAATCCCCGCCATA A G LMNB1 Ensembl:ENSG00000113368 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs967347348 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7375835,Human_RBP_ID_15281432 RMVar_hsa_circ_269995,RMVar_hsa_circ_234100,RMVar_hsa_circ_347816,RMVar_hsa_circ_301602 46796 RMVar_ID_46796 Human_SNP_ID_250389612 A-to-I Human chr5 + 126834345 126834345 126834345 CCCCTGCCTCAGTCTCCCAAGTAGCTGGGATTACAGGCATGCGCCACCACGCCTGGCTAATTTTT CCCCTGCCTCAGTCTCCCAAGTAGCTGGGATTCCAGGCATGCGCCACCACGCCTGGCTAATTTTT A C LMNB1 Ensembl:ENSG00000113368 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1311438734 Functional Loss SNV dbSNP153 33..33 33 - - - 46797 RMVar_ID_46797 Human_SNP_ID_250664193 A-to-I Human chr5 - 127956868 127956868 127956868 CAGACTGGAGTGCAGTGGCATGACCTTGGCTCACTGCAACCTCACCTCTCGGGTTCAAGCGATTC CAGACTGGAGTGCAGTGGCATGACCTTGGCTCGCTGCAACCTCACCTCTCGGGTTCAAGCGATTC T C LINC01184 Ensembl:ENSG00000245937 lincRNA exon GSE38233;GSE107867 cultured B-cells;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 24183664,30559470 RNA-Seq:(High) rs987421249 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_687138,Human_Splice_Rec_687139,Human_Splice_Rec_687144,Human_Splice_Rec_687145,Human_Splice_Rec_687150,Human_Splice_Rec_687151 RMVar_hsa_circ_126759,RMVar_hsa_circ_234120 46798 RMVar_ID_46798 Human_SNP_ID_250664194 A-to-I Human chr5 - 127956868 127956868 127956868 CAGACTGGAGTGCAGTGGCATGACCTTGGCTCACTGCAACCTCACCTCTCGGGTTCAAGCGATTC CAGACTGGAGTGCAGTGGCATGACCTTGGCTCCCTGCAACCTCACCTCTCGGGTTCAAGCGATTC T G LINC01184 Ensembl:ENSG00000245937 lincRNA exon GSE38233;GSE107867 cultured B-cells;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 24183664,30559470 RNA-Seq:(High) rs987421249 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_687138,Human_Splice_Rec_687139,Human_Splice_Rec_687144,Human_Splice_Rec_687145,Human_Splice_Rec_687150,Human_Splice_Rec_687151 RMVar_hsa_circ_126759,RMVar_hsa_circ_234120 46799 RMVar_ID_46799 Human_SNP_ID_250737403 A-to-I Human chr5 - 128258267 128258267 128258267 TTTGTACAATGAATTGATGTTTAGTTTGCTTTAGTCATTTAAAAAGATATTGTACCAGGATGTGC TTTGTACAATGAATTGATGTTTAGTTTGCTTTCGTCATTTAAAAAGATATTGTACCAGGATGTGC T G FBN2 Ensembl:ENSG00000138829 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1419214782 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_630252,Human_RBP_ID_18352519,Human_RBP_ID_24080615,Human_RBP_ID_24503066 RMVar_hsa_circ_106285,RMVar_hsa_circ_234163,RMVar_hsa_circ_90055,RMVar_hsa_circ_234162 46800 RMVar_ID_46800 Human_SNP_ID_250737744 A-to-I Human chr5 - 128259552 128259550 128259553 GGAAATCACTAGCATCCCTCTCTACAAGAAGAAGGAGCTTAAGAAACTGGAAGAGAGCAATGAGG GGAAATCACTAGCATCCCTCTCTACAAGAAG___GAGCTTAAGAAACTGGAAGAGAGCAATGAGG CCTT C FBN2 Ensembl:ENSG00000138829 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1372300289 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_1985712 Human_miRNA_ID_2069889,Human_miRNA_ID_2802789 RMVar_hsa_circ_106285,RMVar_hsa_circ_234163,RMVar_hsa_circ_90055,RMVar_hsa_circ_234162 46801 RMVar_ID_46801 Human_SNP_ID_251411202 A-to-I Human chr5 + 130989931 130989931 130989931 GGCGGATCAAGGTGAAAAGGAGAACCCCATGCAGAAACTTCACATCTGCAAGCTCTGCCTCAACA GGCGGATCAAGGTGAAAAGGAGAACCCCATGCGGAAACTTCACATCTGCAAGCTCTGCCTCAACA A G AC113367.1 Ensembl:ENSG00000244192 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs113083209 Functional Loss SNV dbSNP153 33..33 33 - - - 46802 RMVar_ID_46802 Human_SNP_ID_251411203 A-to-I Human chr5 + 130989931 130989931 130989931 GGCGGATCAAGGTGAAAAGGAGAACCCCATGCAGAAACTTCACATCTGCAAGCTCTGCCTCAACA GGCGGATCAAGGTGAAAAGGAGAACCCCATGCTGAAACTTCACATCTGCAAGCTCTGCCTCAACA A T AC113367.1 Ensembl:ENSG00000244192 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs113083209 Functional Loss SNV dbSNP153 33..33 33 - - - 46803 RMVar_ID_46803 Human_SNP_ID_251411251 A-to-I Human chr5 + 130990115 130990115 130990115 AAATGAAAAGATTGCTGTCCACTGCACAGTTCAAGGATCCAAGGCAGAAGAAATCCTGGAGAAGG AAATGAAAAGATTGCTGTCCACTGCACAGTTCGAGGATCCAAGGCAGAAGAAATCCTGGAGAAGG A G AC113367.1 Ensembl:ENSG00000244192 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879168866 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18058029 46804 RMVar_ID_46804 Human_SNP_ID_251411260 A-to-I Human chr5 + 130990160 130990160 130990160 AGAAGAAATCCTGGAGAAGGATCTAAAGGTGCAGAAGTATGAGTTAAGAAAAAATAACTTCTCAG AGAAGAAATCCTGGAGAAGGATCTAAAGGTGCGGAAGTATGAGTTAAGAAAAAATAACTTCTCAG A G AC113367.1 Ensembl:ENSG00000244192 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879004280 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7492089 46805 RMVar_ID_46805 Human_SNP_ID_251411270 A-to-I Human chr5 + 130990198 130990198 130990198 ATGAGTTAAGAAAAAATAACTTCTCAGATACTAGAAACTTTGGTTTTGGGATCCAGGAACACATC ATGAGTTAAGAAAAAATAACTTCTCAGATACTGGAAACTTTGGTTTTGGGATCCAGGAACACATC A G AC113367.1 Ensembl:ENSG00000244192 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879107353 Functional Loss SNV dbSNP153 33..33 33 - - - 46806 RMVar_ID_46806 Human_SNP_ID_251453589 A-to-I Human chr5 - 131160027 131160027 131160027 CAACATTGGAGAAGCCCCATCTCAACAAAAAAATACAAAAATTAGCCGGGTGTGGTGGCATGTGC CAACATTGGAGAAGCCCCATCTCAACAAAAAATTACAAAAATTAGCCGGGTGTGGTGGCATGTGC T A HINT1 Ensembl:ENSG00000169567 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1022297950 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25936090 46807 RMVar_ID_46807 Human_SNP_ID_251453593 A-to-I Human chr5 - 131160047 131160047 131160047 GAGTTCGAGACCAGCCTGGACAACATTGGAGAAGCCCCATCTCAACAAAAAAATACAAAAATTAG GAGTTCGAGACCAGCCTGGACAACATTGGAGAGGCCCCATCTCAACAAAAAAATACAAAAATTAG T C HINT1 Ensembl:ENSG00000169567 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1029934722 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15286141,Human_RBP_ID_25936090 46808 RMVar_ID_46808 Human_SNP_ID_251453621 A-to-I Human chr5 - 131160144 131160144 131160144 GGAATATAATTAAGTTTTTTTTTTGGTTGGGCATAGTGCCTTGTGCCTGTAATCCCAGCACTTTG GGAATATAATTAAGTTTTTTTTTTGGTTGGGCGTAGTGCCTTGTGCCTGTAATCCCAGCACTTTG T C HINT1 Ensembl:ENSG00000169567 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1561536220 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7378807,Human_RBP_ID_15286143 46809 RMVar_ID_46809 Human_SNP_ID_251453864 A-to-I Human chr5 - 131161378 131161378 131161378 GTTAGTCTCGAACTCCCAACCTCACGTGATCCACCCGCCTCAGCCTTCCAAAGTGCTGGGATTAC GTTAGTCTCGAACTCCCAACCTCACGTGATCCCCCCGCCTCAGCCTTCCAAAGTGCTGGGATTAC T G HINT1 Ensembl:ENSG00000169567 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs974292286 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26252 46810 RMVar_ID_46810 Human_SNP_ID_251453913 A-to-I Human chr5 - 131161551 131161551 131161551 CGTTCTTGTTGCCCAGGCTGGAGTGCAATGGCACGATCTCGGCTCACCGCAACCTCTGCCTCCTG CGTTCTTGTTGCCCAGGCTGGAGTGCAATGGCGCGATCTCGGCTCACCGCAACCTCTGCCTCCTG T C HINT1 Ensembl:ENSG00000169567 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs756076639 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26252 46811 RMVar_ID_46811 Human_SNP_ID_251454084 A-to-I Human chr5 - 131162127 131162126 131162128 GTAGAGACGGCTTTCACCATGTTAGTCAGGATAGTTTCGATTTCCTGACCTCGTGATCCGCCCGC GTAGAGACGGCTTTCACCATGTTAGTCAGGA__GTTTCGATTTCCTGACCTCGTGATCCGCCCGC CTA C HINT1 Ensembl:ENSG00000169567 Protein coding intron GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831 HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line - 29129909,32596459 RNA-Seq:(High) rs199790704 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_15286223 RMVar_hsa_circ_26252,RMVar_hsa_circ_64356 46812 RMVar_ID_46812 Human_SNP_ID_251458501 A-to-I Human chr5 + 131179581 131179581 131179581 GCCTCAACTTCCTAGACTCAAGCAATCCTCCCACTTCAGCCGCCCAAGTAGCTAGGACCACAGGT GCCTCAACTTCCTAGACTCAAGCAATCCTCCCGCTTCAGCCGCCCAAGTAGCTAGGACCACAGGT A G LYRM7 Ensembl:ENSG00000186687 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1172111600 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_234222,RMVar_hsa_circ_123787 46813 RMVar_ID_46813 Human_SNP_ID_251463869 A-to-I Human chr5 + 131201053 131201053 131201053 ATATATTGATATAGGCCCGGGCGCTGTGGCTCACACCTGTAATCCCGCACTTTGGGAGGCTGAGG ATATATTGATATAGGCCCGGGCGCTGTGGCTCGCACCTGTAATCCCGCACTTTGGGAGGCTGAGG A G LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1472843422 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_630458,Human_RBP_ID_788480,Human_RBP_ID_8213554 Human_miRNA_ID_1941757,Human_miRNA_ID_2115948,Human_miRNA_ID_2199522,Human_miRNA_ID_2202589,Human_miRNA_ID_2815052,Human_miRNA_ID_2845144,Human_miRNA_ID_2862315,Human_miRNA_ID_2889797,Human_miRNA_ID_3112041 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 46814 RMVar_ID_46814 Human_SNP_ID_251463870 A-to-I Human chr5 + 131201055 131201055 131201055 ATATTGATATAGGCCCGGGCGCTGTGGCTCACACCTGTAATCCCGCACTTTGGGAGGCTGAGGCG ATATTGATATAGGCCCGGGCGCTGTGGCTCACGCCTGTAATCCCGCACTTTGGGAGGCTGAGGCG A G LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,31158229,31158229 RNA-Seq:(High) rs1164429056 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_788480,Human_RBP_ID_8213554 Human_miRNA_ID_1739752,Human_miRNA_ID_1941757,Human_miRNA_ID_1944804,Human_miRNA_ID_2115948,Human_miRNA_ID_2199522,Human_miRNA_ID_2202589,Human_miRNA_ID_2815052,Human_miRNA_ID_2845144,Human_miRNA_ID_2848166,Human_miRNA_ID_2862315,Human_miRNA_ID_2889797,Human_miRNA_ID_3112041 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 46815 RMVar_ID_46815 Human_SNP_ID_251463871 A-to-I Human chr5 + 131201061 131201061 131201061 ATATAGGCCCGGGCGCTGTGGCTCACACCTGTAATCCCGCACTTTGGGAGGCTGAGGCGGGCAGA ATATAGGCCCGGGCGCTGTGGCTCACACCTGTGATCCCGCACTTTGGGAGGCTGAGGCGGGCAGA A G LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSE38233;GSE100210;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,29129909,31158229,31158229,31158229,31158229 RNA-Seq:(High) rs1383026006 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8213554 Human_miRNA_ID_1941757,Human_miRNA_ID_1944804,Human_miRNA_ID_2085507,Human_miRNA_ID_2115948,Human_miRNA_ID_2199522,Human_miRNA_ID_2202589,Human_miRNA_ID_2815052,Human_miRNA_ID_2845144,Human_miRNA_ID_2848166,Human_miRNA_ID_2862315,Human_miRNA_ID_2889797,Human_miRNA_ID_3112041 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 46816 RMVar_ID_46816 Human_SNP_ID_251463883 A-to-I Human chr5 + 131201104 131201104 131201104 TTGGGAGGCTGAGGCGGGCAGATCACAAGGTCAGGAGTTCGAGACCAGCCTGGCCAATGTGGTGA TTGGGAGGCTGAGGCGGGCAGATCACAAGGTCGGGAGTTCGAGACCAGCCTGGCCAATGTGGTGA A G LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,31158229,31158229 RNA-Seq:(High) rs1326301263 Functional Loss SNV dbSNP153 33..33 33 - - - 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 46817 RMVar_ID_46817 Human_SNP_ID_251463898 A-to-I Human chr5 + 131201152 131201152 131201152 CCTGGCCAATGTGGTGAAACCCCATCTCTACTAAAAACACAAAAATTAGCCAGGTATGGTGGCGG CCTGGCCAATGTGGTGAAACCCCATCTCTACTGAAAACACAAAAATTAGCCAGGTATGGTGGCGG A G LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,31158229,31158229 RNA-Seq:(High) rs1203087450 Functional Loss SNV dbSNP153 33..33 33 - - - 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 46818 RMVar_ID_46818 Human_SNP_ID_251463899 A-to-I Human chr5 + 131201153 131201153 131201153 CTGGCCAATGTGGTGAAACCCCATCTCTACTAAAAACACAAAAATTAGCCAGGTATGGTGGCGGG CTGGCCAATGTGGTGAAACCCCATCTCTACTAGAAACACAAAAATTAGCCAGGTATGGTGGCGGG A G LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSE47997;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;Bronchiolar epithelium,BERP35T1 cell line - 23474544,31158229 RNA-Seq:(High) rs1283492377 Functional Loss SNV dbSNP153 33..33 33 - - - 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 46819 RMVar_ID_46819 Human_SNP_ID_251463994 A-to-I Human chr5 + 131201445 131201445 131201445 AATAAAGTTCCTGAAAGTTCCTGGCTGGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGG AATAAAGTTCCTGAAAGTTCCTGGCTGGGCGCTGTGGCTCACGCCTGTAATCCCAGCACTTTGGG A T LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1404453929 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_630462 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 46820 RMVar_ID_46820 Human_SNP_ID_251463996 A-to-I Human chr5 + 131201453 131201453 131201453 TCCTGAAAGTTCCTGGCTGGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAG TCCTGAAAGTTCCTGGCTGGGCGCAGTGGCTCGCGCCTGTAATCCCAGCACTTTGGGAGGCCGAG A G LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSE38233;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line - 24183664,29796672,31158229 RNA-Seq:(High) rs1469366847 Functional Loss SNV dbSNP153 33..33 33 - - - 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 46821 RMVar_ID_46821 Human_SNP_ID_251464007 A-to-I Human chr5 + 131201488 131201488 131201488 CCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGCAGATCACCTGAGGTCAGGAGTTCTAGACC CCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCAGATCACCTGAGGTCAGGAGTTCTAGACC A G LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line - 24183664,31158229 RNA-Seq:(High) rs887973693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_165984 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 46822 RMVar_ID_46822 Human_SNP_ID_251464013 A-to-I Human chr5 + 131201516 131201516 131201516 AGGCAGGCAGATCACCTGAGGTCAGGAGTTCTAGACCAGCCTGACCAACATGGGGAAACCCTGTC AGGCAGGCAGATCACCTGAGGTCAGGAGTTCTGGACCAGCCTGACCAACATGGGGAAACCCTGTC A G LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1252525674 Functional Loss SNV dbSNP153 33..33 33 - - - 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 46823 RMVar_ID_46823 Human_SNP_ID_251464052 A-to-I Human chr5 + 131201664 131201664 131201664 TTGCTTGAACCCAGGAGACGGAGGTTGCAGTGAGCCGAGATCGCACCATTGCACTCCAGCCTAGG TTGCTTGAACCCAGGAGACGGAGGTTGCAGTGGGCCGAGATCGCACCATTGCACTCCAGCCTAGG A G LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSE38233;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29796672,31158229,31158229,31158229 RNA-Seq:(High) rs1225971161 Functional Loss SNV dbSNP153 33..33 33 - - - 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 46824 RMVar_ID_46824 Human_SNP_ID_251464062 A-to-I Human chr5 + 131201694 131201694 131201694 TGAGCCGAGATCGCACCATTGCACTCCAGCCTAGGCAACAAGAGTGAAACTCCGTCTCAAAAATA TGAGCCGAGATCGCACCATTGCACTCCAGCCTGGGCAACAAGAGTGAAACTCCGTCTCAAAAATA A G LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 29796672,31158229,31158229 RNA-Seq:(High) rs1195030929 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_165985 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 46825 RMVar_ID_46825 Human_SNP_ID_251464099 A-to-I Human chr5 + 131201846 131201846 131201846 TTCTTATATAGCATATGCTAATTTATTTATTTATTTTTTGAGATTGAGTTCTGCTGTGTCACCCA TTCTTATATAGCATATGCTAATTTATTTATTTTTTTTTTGAGATTGAGTTCTGCTGTGTCACCCA A T LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909342257 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7378931,Human_RBP_ID_17575455 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 46826 RMVar_ID_46826 Human_SNP_ID_251464111 A-to-I Human chr5 + 131201909 131201909 131201909 CAGGTTGGAGTGCAGTGGCATGGTCATGGTCCACTAAAGCCTTGACCCCTGGGGCTCAGCAGTTA CAGGTTGGAGTGCAGTGGCATGGTCATGGTCCGCTAAAGCCTTGACCCCTGGGGCTCAGCAGTTA A G LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1186049231 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_630463,Human_RBP_ID_17575289,Human_RBP_ID_26529210 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 46827 RMVar_ID_46827 Human_SNP_ID_251464125 A-to-I Human chr5 + 131201959 131201959 131201959 GGGGCTCAGCAGTTATGCCAACTAAGCCTCCCAAATAGCTGAGACTAGAGGTATGCGCCACCACA GGGGCTCAGCAGTTATGCCAACTAAGCCTCCCGAATAGCTGAGACTAGAGGTATGCGCCACCACA A G LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1384764827 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26520639 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 46828 RMVar_ID_46828 Human_SNP_ID_251464126 A-to-I Human chr5 + 131201960 131201960 131201960 GGGCTCAGCAGTTATGCCAACTAAGCCTCCCAAATAGCTGAGACTAGAGGTATGCGCCACCACAC GGGCTCAGCAGTTATGCCAACTAAGCCTCCCAGATAGCTGAGACTAGAGGTATGCGCCACCACAC A G LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs1420090544 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26520639 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 46829 RMVar_ID_46829 Human_SNP_ID_251464129 A-to-I Human chr5 + 131201968 131201968 131201968 CAGTTATGCCAACTAAGCCTCCCAAATAGCTGAGACTAGAGGTATGCGCCACCACACCTAGCTAT CAGTTATGCCAACTAAGCCTCCCAAATAGCTGGGACTAGAGGTATGCGCCACCACACCTAGCTAT A G LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSE100210;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229 RNA-Seq:(High) rs1343395585 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26520639 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 46830 RMVar_ID_46830 Human_SNP_ID_251464130 A-to-I Human chr5 + 131201973 131201973 131201973 ATGCCAACTAAGCCTCCCAAATAGCTGAGACTAGAGGTATGCGCCACCACACCTAGCTATTTTTT ATGCCAACTAAGCCTCCCAAATAGCTGAGACTGGAGGTATGCGCCACCACACCTAGCTATTTTTT A G LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSE100210;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229 RNA-Seq:(High) rs1452930735 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26520639 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 46831 RMVar_ID_46831 Human_SNP_ID_251464138 A-to-I Human chr5 + 131201995 131201995 131201995 AGCTGAGACTAGAGGTATGCGCCACCACACCTAGCTATTTTTTTTATTTTTAGTAAGGACAAGGT AGCTGAGACTAGAGGTATGCGCCACCACACCTGGCTATTTTTTTTATTTTTAGTAAGGACAAGGT A G LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs1313943640 Functional Loss SNV dbSNP153 33..33 33 - - - 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 46832 RMVar_ID_46832 Human_SNP_ID_251464144 A-to-I Human chr5 + 131202017 131202017 131202017 CACCACACCTAGCTATTTTTTTTATTTTTAGTAAGGACAAGGTCTCATTATGTTGGCCAGGCTGG CACCACACCTAGCTATTTTTTTTATTTTTAGTGAGGACAAGGTCTCATTATGTTGGCCAGGCTGG A G LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSE38233;GSE100210;GSE100210;GSE107867;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;HepG2 cell line;ASD brains,frontal_cortex;Bronchiolar epithelium,BERP35T4 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,29129909,30559470,31158229,31158229 RNA-Seq:(High) rs1309569328 Functional Loss SNV dbSNP153 33..33 33 - - - 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 46833 RMVar_ID_46833 Human_SNP_ID_251464146 A-to-I Human chr5 + 131202023 131202023 131202023 ACCTAGCTATTTTTTTTATTTTTAGTAAGGACAAGGTCTCATTATGTTGGCCAGGCTGGTCTCAA ACCTAGCTATTTTTTTTATTTTTAGTAAGGACGAGGTCTCATTATGTTGGCCAGGCTGGTCTCAA A G LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs560954054 Functional Loss SNV dbSNP153 33..33 33 - - - 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 46834 RMVar_ID_46834 Human_SNP_ID_251464152 A-to-I Human chr5 + 131202043 131202043 131202043 TTTAGTAAGGACAAGGTCTCATTATGTTGGCCAGGCTGGTCTCAAATTCCTGAGCTCAGTTGATC TTTAGTAAGGACAAGGTCTCATTATGTTGGCCGGGCTGGTCTCAAATTCCTGAGCTCAGTTGATC A G LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSE100210;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229 RNA-Seq:(High) rs967262509 Functional Loss SNV dbSNP153 33..33 33 - - - 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 46835 RMVar_ID_46835 Human_SNP_ID_251464153 A-to-I Human chr5 + 131202043 131202043 131202043 TTTAGTAAGGACAAGGTCTCATTATGTTGGCCAGGCTGGTCTCAAATTCCTGAGCTCAGTTGATC TTTAGTAAGGACAAGGTCTCATTATGTTGGCCTGGCTGGTCTCAAATTCCTGAGCTCAGTTGATC A T LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSE100210;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229 RNA-Seq:(High) rs967262509 Functional Loss SNV dbSNP153 33..33 33 - - - 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 46836 RMVar_ID_46836 Human_SNP_ID_251464155 A-to-I Human chr5 + 131202081 131202054 131202091 GTCTCAAATTCCTGAGCTCAGTTGATCCTCCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGT GTCTCGAACTTCCGACCTCAGGTAATCCACCTGCCTCAGCCTGCCAAAGTGCTGGGATTACAGGT AAATTCCTGAGCTCAGTTGATCCTCCCACCTCAGCCTC GAACTTCCGACCTCAGGTAATCCACCTGCCTCAGCCTG LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSE100210;GSE99789 HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 29129909,29796672 RNA-Seq:(High) rs71591222 Functional Loss MNV dbSNP153 6..43 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 46837 RMVar_ID_46837 Human_SNP_ID_251464155 A-to-I Human chr5 + 131202054 131202054 131202091 CAAGGTCTCATTATGTTGGCCAGGCTGGTCTCAAATTCCTGAGCTCAGTTGATCCTCCCACCTCA CAAGGTCTCATTATGTTGGCCAGGCTGGTCTCGAACTTCCGACCTCAGGTAATCCACCTGCCTCA AAATTCCTGAGCTCAGTTGATCCTCCCACCTCAGCCTC GAACTTCCGACCTCAGGTAATCCACCTGCCTCAGCCTG LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSE100210;GSE99789 HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 29129909,29796672 RNA-Seq:(High) rs71591222 Functional Loss MNV dbSNP153 33..65 33 - - - 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 46838 RMVar_ID_46838 Human_SNP_ID_251464155 A-to-I Human chr5 + 131202086 131202054 131202091 AAATTCCTGAGCTCAGTTGATCCTCCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTAAG GAACTTCCGACCTCAGGTAATCCACCTGCCTCAGCCTGCCAAAGTGCTGGGATTACAGGTGTAAG AAATTCCTGAGCTCAGTTGATCCTCCCACCTCAGCCTC GAACTTCCGACCTCAGGTAATCCACCTGCCTCAGCCTG LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSE100210;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229 RNA-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 46839 RMVar_ID_46839 Human_SNP_ID_251464156 A-to-I Human chr5 + 131202054 131202054 131202054 CAAGGTCTCATTATGTTGGCCAGGCTGGTCTCAAATTCCTGAGCTCAGTTGATCCTCCCACCTCA CAAGGTCTCATTATGTTGGCCAGGCTGGTCTCGAATTCCTGAGCTCAGTTGATCCTCCCACCTCA A G LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSE100210;GSE99789 HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 29129909,29796672 RNA-Seq:(High) rs1462712322 Functional Loss SNV dbSNP153 33..33 33 - - - 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 46840 RMVar_ID_46840 Human_SNP_ID_251464169 A-to-I Human chr5 + 131202108 131202108 131202108 CTCCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTAAGCCACTGCACCCTGCCTATTCTT CTCCCACCTCAGCCTCCCAAAGTGCTGGGATTGCAGGTGTAAGCCACTGCACCCTGCCTATTCTT A G LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs566157473 Functional Loss SNV dbSNP153 33..33 33 - - - 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 46841 RMVar_ID_46841 Human_SNP_ID_251464194 A-to-I Human chr5 + 131202231 131202231 131202231 ATAAAGTAATTCATGGCTGGGTGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGCAGGCTGAG ATAAAGTAATTCATGGCTGGGTGTGGTGGCTCGCGCCTGTAATCCCAGCACTTTGGCAGGCTGAG A G LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1170698793 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17575721,Human_RBP_ID_26529808 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 46842 RMVar_ID_46842 Human_SNP_ID_251464197 A-to-I Human chr5 + 131202239 131202239 131202239 ATTCATGGCTGGGTGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGCAGGCTGAGGCAGGTGG ATTCATGGCTGGGTGTGGTGGCTCACGCCTGTGATCCCAGCACTTTGGCAGGCTGAGGCAGGTGG A G LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSE38233;GSE100210;GSE99789 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 24183664,29129909,29796672 RNA-Seq:(High) rs1221794088 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17575721,Human_RBP_ID_26529808 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 46843 RMVar_ID_46843 Human_SNP_ID_251464215 A-to-I Human chr5 + 131202304 131202304 131202304 ATTACCTGAGGTCGGAAGTTCGAGACCAGCCCAACCAACGTGGAGAAACCCCATCTCTATTAAAA ATTACCTGAGGTCGGAAGTTCGAGACCAGCCCGACCAACGTGGAGAAACCCCATCTCTATTAAAA A G LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSE38233;GSE100210;GSE100210;GSE99789;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;HepG2 cell line;esophageal squamous carcinoma cells,EC109;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,29129909,29796672,30559470,31158229,31158229,32596459 RNA-Seq:(High) rs1411376254 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17706876 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 46844 RMVar_ID_46844 Human_SNP_ID_251464224 A-to-I Human chr5 + 131202347 131202347 131202347 AGAAACCCCATCTCTATTAAAAATGCAAAATTAGCAGGACATGGTGATACACACCTGTAATCCCA AGAAACCCCATCTCTATTAAAAATGCAAAATTGGCAGGACATGGTGATACACACCTGTAATCCCA A G LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1353499711 Functional Loss SNV dbSNP153 33..33 33 - - - 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 46845 RMVar_ID_46845 Human_SNP_ID_251464236 A-to-I Human chr5 + 131202379 131202379 131202379 AGCAGGACATGGTGATACACACCTGTAATCCCAGCTAGTCAGGAGGCTGAGGCAGGAGAATTACT AGCAGGACATGGTGATACACACCTGTAATCCCGGCTAGTCAGGAGGCTGAGGCAGGAGAATTACT A G LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSE38233;GSE100210;GSE99789;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,29796672,31158229,31158229 RNA-Seq:(High) rs1216334956 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26520641 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 46846 RMVar_ID_46846 Human_SNP_ID_251464237 A-to-I Human chr5 + 131202383 131202383 131202383 GGACATGGTGATACACACCTGTAATCCCAGCTAGTCAGGAGGCTGAGGCAGGAGAATTACTTGAG GGACATGGTGATACACACCTGTAATCCCAGCTGGTCAGGAGGCTGAGGCAGGAGAATTACTTGAG A G LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSE38233;GSE100210;GSE99789;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,29796672,31158229,32596459 RNA-Seq:(High) rs1271175284 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26520641 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 46847 RMVar_ID_46847 Human_SNP_ID_251464239 A-to-I Human chr5 + 131202387 131202387 131202387 ATGGTGATACACACCTGTAATCCCAGCTAGTCAGGAGGCTGAGGCAGGAGAATTACTTGAGCCAG ATGGTGATACACACCTGTAATCCCAGCTAGTCGGGAGGCTGAGGCAGGAGAATTACTTGAGCCAG A G LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSE38233;GSE100210;GSE99789;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,29796672,31158229,32596459 RNA-Seq:(High) rs1307095994 Functional Loss SNV dbSNP153 33..33 33 - - - 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 46848 RMVar_ID_46848 Human_SNP_ID_251464253 A-to-I Human chr5 + 131202443 131202443 131202443 TTGAGCCAGGGAAGCAGAGGTTGTGGTGAGCTAAGATTGTGCCACTGCACTCCAGCCTGAGAGAA TTGAGCCAGGGAAGCAGAGGTTGTGGTGAGCTGAGATTGTGCCACTGCACTCCAGCCTGAGAGAA A G LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSE38233;GSE100210;GSE99789;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,29796672,29796672,31158229,31158229,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs1223003654 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26529213 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 46849 RMVar_ID_46849 Human_SNP_ID_251464282 A-to-I Human chr5 + 131202544 131202544 131202544 TTTTTACACATGGGTATCTCACCATGTTGCCCAGGCTGGAGTGCAGTAGCTATTCATAGGCACAG TTTTTACACATGGGTATCTCACCATGTTGCCCTGGCTGGAGTGCAGTAGCTATTCATAGGCACAG A T LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1412922655 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17575722 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 46850 RMVar_ID_46850 Human_SNP_ID_251464307 A-to-I Human chr5 + 131202611 131202611 131202611 ATAGCACACTGCAGCCTAGAATTTCTGACCTCAAGCAATCATCCTGCCTCAGCCTCCTAAGTAGC ATAGCACACTGCAGCCTAGAATTTCTGACCTCCAGCAATCATCCTGCCTCAGCCTCCTAAGTAGC A C LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSE100210;GSE99789;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831 HepG2 cell line;esophageal squamous carcinoma cells,EC109;ASD brains,frontal_cortex;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line - 29129909,29796672,30559470,31158229,31158229,31158229,32596459 RNA-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 46851 RMVar_ID_46851 Human_SNP_ID_251464308 A-to-I Human chr5 + 131202611 131202611 131202611 ATAGCACACTGCAGCCTAGAATTTCTGACCTCAAGCAATCATCCTGCCTCAGCCTCCTAAGTAGC ATAGCACACTGCAGCCTAGAATTTCTGACCTCGAGCAATCATCCTGCCTCAGCCTCCTAAGTAGC A G LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSE100210;GSE99789;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831 HepG2 cell line;esophageal squamous carcinoma cells,EC109;ASD brains,frontal_cortex;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line - 29129909,29796672,30559470,31158229,31158229,31158229,32596459 RNA-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 46852 RMVar_ID_46852 Human_SNP_ID_251464315 A-to-I Human chr5 + 131202637 131202637 131202637 GACCTCAAGCAATCATCCTGCCTCAGCCTCCTAAGTAGCTAGGACTACAGGTGCATACCACCATA GACCTCAAGCAATCATCCTGCCTCAGCCTCCTGAGTAGCTAGGACTACAGGTGCATACCACCATA A G LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSE47997;GSE38233;GSE38233;GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490829,GSM3490830,GSM3490831 K562 cells&HepG2 cells;cultured B-cells;cultured B-cells;HepG2 cell line;ASD brains,frontal_cortex;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,EC109 cell line - 23474544,24183664,24183664,29129909,30559470,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs1213080343 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 46853 RMVar_ID_46853 Human_SNP_ID_251464317 A-to-I Human chr5 + 131202645 131202645 131202645 GCAATCATCCTGCCTCAGCCTCCTAAGTAGCTAGGACTACAGGTGCATACCACCATAACCAGCTT GCAATCATCCTGCCTCAGCCTCCTAAGTAGCTGGGACTACAGGTGCATACCACCATAACCAGCTT A G LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,31158229,31158229,31158229,32596459 RNA-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 46854 RMVar_ID_46854 Human_SNP_ID_251464318 A-to-I Human chr5 + 131202651 131202651 131202651 ATCCTGCCTCAGCCTCCTAAGTAGCTAGGACTACAGGTGCATACCACCATAACCAGCTTTAATTA ATCCTGCCTCAGCCTCCTAAGTAGCTAGGACTCCAGGTGCATACCACCATAACCAGCTTTAATTA A C LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSE38233;GSE99789 cultured B-cells;esophageal squamous carcinoma cells,EC109 - 24183664,29796672 RNA-Seq:(High) rs889030112 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 46855 RMVar_ID_46855 Human_SNP_ID_251464319 A-to-I Human chr5 + 131202651 131202651 131202651 ATCCTGCCTCAGCCTCCTAAGTAGCTAGGACTACAGGTGCATACCACCATAACCAGCTTTAATTA ATCCTGCCTCAGCCTCCTAAGTAGCTAGGACTGCAGGTGCATACCACCATAACCAGCTTTAATTA A G LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSE38233;GSE99789 cultured B-cells;esophageal squamous carcinoma cells,EC109 - 24183664,29796672 RNA-Seq:(High) rs889030112 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 46856 RMVar_ID_46856 Human_SNP_ID_251464492 A-to-I Human chr5 + 131203422 131203422 131203422 CAGTTTTTCAAAAATCTATTGAGGCCAGGTGCAGTGGCCCATGCCTGTAGTTCCAGTACTTTGGG CAGTTTTTCAAAAATCTATTGAGGCCAGGTGCGGTGGCCCATGCCTGTAGTTCCAGTACTTTGGG A G LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1022494330 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18037827,Human_RBP_ID_26529812 Human_miRNA_ID_621812,Human_miRNA_ID_1473283,Human_miRNA_ID_2492661,Human_miRNA_ID_2750285 RMVar_hsa_circ_75865,RMVar_hsa_circ_234222,RMVar_hsa_circ_123787,RMVar_hsa_circ_83267,RMVar_hsa_circ_234227,RMVar_hsa_circ_80415,RMVar_hsa_circ_234229,RMVar_hsa_circ_234230 46857 RMVar_ID_46857 Human_SNP_ID_251464654 A-to-I Human chr5 + 131204122 131204122 131204122 TTTGTTTCTTTGGGTTTTTTTTTTTTAGAGACAAGATCTCTCCGTGTTGTCTAGGCTGGACTCAA TTTGTTTCTTTGGGTTTTTTTTTTTTAGAGACGAGATCTCTCCGTGTTGTCTAGGCTGGACTCAA A G LYRM7 Ensembl:ENSG00000186687 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs187499835 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7378953,Human_RBP_ID_26530437 RMVar_hsa_circ_75865,RMVar_hsa_circ_234222,RMVar_hsa_circ_123787,RMVar_hsa_circ_83267,RMVar_hsa_circ_234227,RMVar_hsa_circ_80415,RMVar_hsa_circ_234229,RMVar_hsa_circ_234230 46858 RMVar_ID_46858 Human_SNP_ID_251481565 A-to-I Human chr5 + 131276191 131276191 131276191 AATCTTGGCCAGGTGCGATAGGCTAAGTCTGTAGTCCCAGCACTTTGGGAGGCTGAGGTGAGTGG AATCTTGGCCAGGTGCGATAGGCTAAGTCTGTGGTCCCAGCACTTTGGGAGGCTGAGGTGAGTGG A G CDC42SE2 Ensembl:ENSG00000158985 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs796151284 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3782810,Human_RBP_ID_9436711,Human_RBP_ID_17575291 RMVar_hsa_circ_329116 46859 RMVar_ID_46859 Human_SNP_ID_251484802 A-to-I Human chr5 + 131287602 131287602 131287602 CTCCCACCTCAGCCTCCCAAGTCGGTGGGACTATAGGTGTGTGCCACCATGCCCAGCTTTTTTTT CTCCCACCTCAGCCTCCCAAGTCGGTGGGACTGTAGGTGTGTGCCACCATGCCCAGCTTTTTTTT A G CDC42SE2 Ensembl:ENSG00000158985 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs534979400 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7379086 RMVar_hsa_circ_329116 46860 RMVar_ID_46860 Human_SNP_ID_251485049 A-to-I Human chr5 + 131288531 131288531 131288531 GATTCCTTTTTTTTTAGAGAGAGCCTCACTCTATGGTCCAGGCTGAAGTGCAGTGGTGCAGTCAT GATTCCTTTTTTTTTAGAGAGAGCCTCACTCTGTGGTCCAGGCTGAAGTGCAGTGGTGCAGTCAT A G CDC42SE2 Ensembl:ENSG00000158985 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1004578319 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_329116 46861 RMVar_ID_46861 Human_SNP_ID_251494299 A-to-I Human chr5 + 131321430 131321430 131321430 TGCTGATAGTCCTAGTTATTTGGGAGGCTGATAGGGAAGGATTGTTTGAACTCAGGAGTTCAAAT TGCTGATAGTCCTAGTTATTTGGGAGGCTGATGGGGAAGGATTGTTTGAACTCAGGAGTTCAAAT A G CDC42SE2 Ensembl:ENSG00000158985 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs558497182 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54820,RMVar_hsa_circ_73356,RMVar_hsa_circ_20939 46862 RMVar_ID_46862 Human_SNP_ID_251506434 A-to-I Human chr5 + 131363432 131363432 131363432 GAGTTTTGCTCTTGTCGCCTAGGCTGGAGTGCAATGGTGCGATCTTGGCTCACTGCAACCTCTGC GAGTTTTGCTCTTGTCGCCTAGGCTGGAGTGCCATGGTGCGATCTTGGCTCACTGCAACCTCTGC A C CDC42SE2 Ensembl:ENSG00000158985 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1290944478 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1442,RMVar_hsa_circ_54820,RMVar_hsa_circ_20939,RMVar_hsa_circ_124691,RMVar_hsa_circ_234233 46863 RMVar_ID_46863 Human_SNP_ID_251506469 A-to-I Human chr5 + 131363557 131363557 131363557 CTCCACCATGCCCAGCTAATTTTTGTAGTTTCAGTAGAGATGGGGTTTCTCCATGTTAGCCAGGC CTCCACCATGCCCAGCTAATTTTTGTAGTTTCGGTAGAGATGGGGTTTCTCCATGTTAGCCAGGC A G CDC42SE2 Ensembl:ENSG00000158985 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs966492461 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1442,RMVar_hsa_circ_54820,RMVar_hsa_circ_20939,RMVar_hsa_circ_124691,RMVar_hsa_circ_234233 46864 RMVar_ID_46864 Human_SNP_ID_251507284 A-to-I Human chr5 + 131366917 131366917 131366917 GTGTGTGGTAGTGTGTGCCTGTAGGCCCAGCTACTCGGGAGGCTGAGGTAGGAGGATTGCTTGAG GTGTGTGGTAGTGTGTGCCTGTAGGCCCAGCTGCTCGGGAGGCTGAGGTAGGAGGATTGCTTGAG A G CDC42SE2 Ensembl:ENSG00000158985 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs907695131 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1442,RMVar_hsa_circ_54820,RMVar_hsa_circ_20939,RMVar_hsa_circ_124691,RMVar_hsa_circ_234233 46865 RMVar_ID_46865 Human_SNP_ID_251521405 A-to-I Human chr5 - 131424177 131424177 131424177 CTAATCAGCAAAAGACAGAAACAAAACTGCACATCTGTAATAATCAGATAGCAATTCTACTGCAC CTAATCAGCAAAAGACAGAAACAAAACTGCACGTCTGTAATAATCAGATAGCAATTCTACTGCAC T C RAPGEF6 Ensembl:ENSG00000158987 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs547668242 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1643933,Human_RBP_ID_1985910,Human_RBP_ID_18831609,Human_RBP_ID_27733995 Human_miRNA_ID_128372,Human_miRNA_ID_628449 46866 RMVar_ID_46866 Human_SNP_ID_251522335 A-to-I Human chr5 - 131428291 131428291 131428291 CTCCCAACTCAGCCTCCCAAGTAGCTGGGACTACAGGTGCACACCAGCATGCCTGGCTCATTGTT CTCCCAACTCAGCCTCCCAAGTAGCTGGGACTGCAGGTGCACACCAGCATGCCTGGCTCATTGTT T C AC008695.1,RAPGEF6 Ensembl:ENSG00000273217,Ensembl:ENSG00000158987 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1381541882 Functional Loss SNV dbSNP153 33..33 33 - - - 46867 RMVar_ID_46867 Human_SNP_ID_251522339 A-to-I Human chr5 - 131428305 131428305 131428305 GGGCTCAAGCAGTCCTCCCAACTCAGCCTCCCAAGTAGCTGGGACTACAGGTGCACACCAGCATG GGGCTCAAGCAGTCCTCCCAACTCAGCCTCCCGAGTAGCTGGGACTACAGGTGCACACCAGCATG T C AC008695.1,RAPGEF6 Ensembl:ENSG00000273217,Ensembl:ENSG00000158987 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs946510079 Functional Loss SNV dbSNP153 33..33 33 - - - 46868 RMVar_ID_46868 Human_SNP_ID_251522437 A-to-I Human chr5 - 131428663 131428663 131428663 GAGGTCGGGAGTTCCTGACCAGCCTGTCCAACATGGAGAAACCCCGTCTCTACTAAAAAAATACA GAGGTCGGGAGTTCCTGACCAGCCTGTCCAACGTGGAGAAACCCCGTCTCTACTAAAAAAATACA T C AC008695.1,RAPGEF6 Ensembl:ENSG00000273217,Ensembl:ENSG00000158987 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs958974538 Functional Loss SNV dbSNP153 33..33 33 - - - 46869 RMVar_ID_46869 Human_SNP_ID_251522457 A-to-I Human chr5 - 131428734 131428734 131428734 CTGCCGGCAGGGTGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGCGAA CTGCCGGCAGGGTGCAGTGGCTCACACCTGTAGTCCCAGCACTTTGGGAGGCTGAGGCGGGCGAA T C AC008695.1,RAPGEF6 Ensembl:ENSG00000273217,Ensembl:ENSG00000158987 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1384246652 Functional Loss SNV dbSNP153 33..33 33 - - - 46870 RMVar_ID_46870 Human_SNP_ID_251533928 A-to-I Human chr5 - 131476351 131476351 131476351 GAACTCCTGACCTCAGGTGATCCACGCGCCTCAGCCTCACAGAGTGCTGGGATTACAGGTTTGAG GAACTCCTGACCTCAGGTGATCCACGCGCCTCGGCCTCACAGAGTGCTGGGATTACAGGTTTGAG T C AC008695.1,RAPGEF6 Ensembl:ENSG00000273217,Ensembl:ENSG00000158987 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1290837957 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39160,RMVar_hsa_circ_63553,RMVar_hsa_circ_15942,RMVar_hsa_circ_28670,RMVar_hsa_circ_79001,RMVar_hsa_circ_234245,RMVar_hsa_circ_275868,RMVar_hsa_circ_265261,RMVar_hsa_circ_321118,RMVar_hsa_circ_48286,RMVar_hsa_circ_306129,RMVar_hsa_circ_326977,RMVar_hsa_circ_339122,RMVar_hsa_circ_234250,RMVar_hsa_circ_344897,RMVar_hsa_circ_112852,RMVar_hsa_circ_54615,RMVar_hsa_circ_234254,RMVar_hsa_circ_234256,RMVar_hsa_circ_234255,RMVar_hsa_circ_234253,RMVar_hsa_circ_16748,RMVar_hsa_circ_317427,RMVar_hsa_circ_61075,RMVar_hsa_circ_318869,RMVar_hsa_circ_234257,RMVar_hsa_circ_281455,RMVar_hsa_circ_18582,RMVar_hsa_circ_31171,RMVar_hsa_circ_22725,RMVar_hsa_circ_234260,RMVar_hsa_circ_296646,RMVar_hsa_circ_372094,RMVar_hsa_circ_234261,RMVar_hsa_circ_234262 46871 RMVar_ID_46871 Human_SNP_ID_251539697 A-to-I Human chr5 - 131500027 131500027 131500027 GGGCATAGTGGTGCATGCCTGTAATTGCAGCTACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAA GGGCATAGTGGTGCATGCCTGTAATTGCAGCTGCTCAGGAGGCTGAGGCAGGAGAATTGCTTGAA T C AC008695.1,RAPGEF6 Ensembl:ENSG00000273217,Ensembl:ENSG00000158987 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs540456391 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7005,RMVar_hsa_circ_39160,RMVar_hsa_circ_15942,RMVar_hsa_circ_28670,RMVar_hsa_circ_275868,RMVar_hsa_circ_321118,RMVar_hsa_circ_306129,RMVar_hsa_circ_326977,RMVar_hsa_circ_339122,RMVar_hsa_circ_234250,RMVar_hsa_circ_112852,RMVar_hsa_circ_234254,RMVar_hsa_circ_234256,RMVar_hsa_circ_234255,RMVar_hsa_circ_317427,RMVar_hsa_circ_318869,RMVar_hsa_circ_234257,RMVar_hsa_circ_281455,RMVar_hsa_circ_62651,RMVar_hsa_circ_31171,RMVar_hsa_circ_234260,RMVar_hsa_circ_296646,RMVar_hsa_circ_372094,RMVar_hsa_circ_234261,RMVar_hsa_circ_234262,RMVar_hsa_circ_287820,RMVar_hsa_circ_234263,RMVar_hsa_circ_115166,RMVar_hsa_circ_13835,RMVar_hsa_circ_10499,RMVar_hsa_circ_304639,RMVar_hsa_circ_331381,RMVar_hsa_circ_234264,RMVar_hsa_circ_316668,RMVar_hsa_circ_234265,RMVar_hsa_circ_234266,RMVar_hsa_circ_41943,RMVar_hsa_circ_66086,RMVar_hsa_circ_703,RMVar_hsa_circ_315122,RMVar_hsa_circ_349975,RMVar_hsa_circ_41454,RMVar_hsa_circ_46375,RMVar_hsa_circ_292646,RMVar_hsa_circ_234268,RMVar_hsa_circ_363947,RMVar_hsa_circ_57018,RMVar_hsa_circ_234269 46872 RMVar_ID_46872 Human_SNP_ID_251547332 A-to-I Human chr5 - 131529738 131529738 131529738 CTGGCCAATTTTCTAATTTTTTTGTAGAGACAAGGTCTCTCCATCTTGCCCAAGCTGGTCTCAAA CTGGCCAATTTTCTAATTTTTTTGTAGAGACAGGGTCTCTCCATCTTGCCCAAGCTGGTCTCAAA T C AC008695.1,RAPGEF6 Ensembl:ENSG00000273217,Ensembl:ENSG00000158987 Protein coding,Protein coding intron,intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1355998356 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39160,RMVar_hsa_circ_275868,RMVar_hsa_circ_321118,RMVar_hsa_circ_306129,RMVar_hsa_circ_234250,RMVar_hsa_circ_317427,RMVar_hsa_circ_234257,RMVar_hsa_circ_281455,RMVar_hsa_circ_234260,RMVar_hsa_circ_296646,RMVar_hsa_circ_372094,RMVar_hsa_circ_234261,RMVar_hsa_circ_234262,RMVar_hsa_circ_287820,RMVar_hsa_circ_234263,RMVar_hsa_circ_115166,RMVar_hsa_circ_13835,RMVar_hsa_circ_24368,RMVar_hsa_circ_304639,RMVar_hsa_circ_331381,RMVar_hsa_circ_234264,RMVar_hsa_circ_234266,RMVar_hsa_circ_41943,RMVar_hsa_circ_703,RMVar_hsa_circ_315122,RMVar_hsa_circ_234268,RMVar_hsa_circ_363947,RMVar_hsa_circ_284298,RMVar_hsa_circ_321810,RMVar_hsa_circ_72930,RMVar_hsa_circ_234274,RMVar_hsa_circ_338374,RMVar_hsa_circ_234275,RMVar_hsa_circ_353571,RMVar_hsa_circ_234276,RMVar_hsa_circ_234278,RMVar_hsa_circ_124422,RMVar_hsa_circ_334001,RMVar_hsa_circ_338175,RMVar_hsa_circ_278869,RMVar_hsa_circ_234279,RMVar_hsa_circ_234277 46873 RMVar_ID_46873 Human_SNP_ID_251547444 A-to-I Human chr5 - 131530072 131530072 131530072 GAAACCCCGTGTCTATTAAAAATATAAAAATTAGCCAGGTGTGGTGCCACATATCTGTAGTCCCA GAAACCCCGTGTCTATTAAAAATATAAAAATTGGCCAGGTGTGGTGCCACATATCTGTAGTCCCA T C AC008695.1,RAPGEF6 Ensembl:ENSG00000273217,Ensembl:ENSG00000158987 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1141093 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39160,RMVar_hsa_circ_275868,RMVar_hsa_circ_321118,RMVar_hsa_circ_306129,RMVar_hsa_circ_234250,RMVar_hsa_circ_317427,RMVar_hsa_circ_234257,RMVar_hsa_circ_281455,RMVar_hsa_circ_234260,RMVar_hsa_circ_296646,RMVar_hsa_circ_372094,RMVar_hsa_circ_234261,RMVar_hsa_circ_234262,RMVar_hsa_circ_287820,RMVar_hsa_circ_234263,RMVar_hsa_circ_115166,RMVar_hsa_circ_13835,RMVar_hsa_circ_24368,RMVar_hsa_circ_304639,RMVar_hsa_circ_331381,RMVar_hsa_circ_234264,RMVar_hsa_circ_234266,RMVar_hsa_circ_41943,RMVar_hsa_circ_703,RMVar_hsa_circ_315122,RMVar_hsa_circ_234268,RMVar_hsa_circ_363947,RMVar_hsa_circ_284298,RMVar_hsa_circ_321810,RMVar_hsa_circ_72930,RMVar_hsa_circ_234274,RMVar_hsa_circ_338374,RMVar_hsa_circ_234275,RMVar_hsa_circ_353571,RMVar_hsa_circ_234276,RMVar_hsa_circ_234278,RMVar_hsa_circ_124422,RMVar_hsa_circ_334001,RMVar_hsa_circ_338175,RMVar_hsa_circ_278869,RMVar_hsa_circ_234279,RMVar_hsa_circ_234277 46874 RMVar_ID_46874 Human_SNP_ID_251575984 A-to-I Human chr5 - 131648113 131648113 131648113 GTTGCCCAGGCTGATCTCGAACTCCTGGCCTCAGATGATCCTCCTGCCTCCACCTCCCAGAATGT GTTGCCCAGGCTGATCTCGAACTCCTGGCCTCCGATGATCCTCCTGCCTCCACCTCCCAGAATGT T G FNIP1,AC008695.1 Ensembl:ENSG00000217128,Ensembl:ENSG00000273217 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223439391 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95431,RMVar_hsa_circ_123864,RMVar_hsa_circ_114349,RMVar_hsa_circ_119082,RMVar_hsa_circ_98414,RMVar_hsa_circ_234292,RMVar_hsa_circ_83654,RMVar_hsa_circ_93710,RMVar_hsa_circ_93850,RMVar_hsa_circ_91175,RMVar_hsa_circ_234296,RMVar_hsa_circ_76695,RMVar_hsa_circ_79178,RMVar_hsa_circ_234297,RMVar_hsa_circ_234294,RMVar_hsa_circ_234295,RMVar_hsa_circ_234293,RMVar_hsa_circ_234288,RMVar_hsa_circ_234290,RMVar_hsa_circ_234291,RMVar_hsa_circ_234289,RMVar_hsa_circ_127680,RMVar_hsa_circ_312259,RMVar_hsa_circ_234287,RMVar_hsa_circ_341545,RMVar_hsa_circ_295361,RMVar_hsa_circ_234300,RMVar_hsa_circ_64913,RMVar_hsa_circ_234301,RMVar_hsa_circ_234299 46875 RMVar_ID_46875 Human_SNP_ID_251577042 A-to-I Human chr5 - 131652950 131652950 131652950 TGTTGTTTGTGTTTTTTTTAAGACAGGGTCTTACTCTTTGACCCACACTGGAGGGCTGTGGCACA TGTTGTTTGTGTTTTTTTTAAGACAGGGTCTTGCTCTTTGACCCACACTGGAGGGCTGTGGCACA T C FNIP1,AC008695.1 Ensembl:ENSG00000217128,Ensembl:ENSG00000273217 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs778387385 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3756795,Human_RBP_ID_7380278 RMVar_hsa_circ_60608,RMVar_hsa_circ_95431,RMVar_hsa_circ_123864,RMVar_hsa_circ_114349,RMVar_hsa_circ_119082,RMVar_hsa_circ_98414,RMVar_hsa_circ_234292,RMVar_hsa_circ_83654,RMVar_hsa_circ_93710,RMVar_hsa_circ_93850,RMVar_hsa_circ_91175,RMVar_hsa_circ_234296,RMVar_hsa_circ_76695,RMVar_hsa_circ_79178,RMVar_hsa_circ_234297,RMVar_hsa_circ_234294,RMVar_hsa_circ_234295,RMVar_hsa_circ_234293,RMVar_hsa_circ_234288,RMVar_hsa_circ_234290,RMVar_hsa_circ_234291,RMVar_hsa_circ_234289,RMVar_hsa_circ_127680,RMVar_hsa_circ_312259,RMVar_hsa_circ_234287,RMVar_hsa_circ_341545,RMVar_hsa_circ_234300,RMVar_hsa_circ_64913,RMVar_hsa_circ_234301,RMVar_hsa_circ_367832,RMVar_hsa_circ_290384,RMVar_hsa_circ_43505,RMVar_hsa_circ_55927,RMVar_hsa_circ_234303,RMVar_hsa_circ_234304 46876 RMVar_ID_46876 Human_SNP_ID_251579507 A-to-I Human chr5 - 131662807 131662807 131662807 TGAACCTGGGAAGCCAAGGTTGTGGTGAGCCAAGATCGTGCCACTGTACTCCAGCCTGGGTGACA TGAACCTGGGAAGCCAAGGTTGTGGTGAGCCAGGATCGTGCCACTGTACTCCAGCCTGGGTGACA T C FNIP1,AC008695.1 Ensembl:ENSG00000217128,Ensembl:ENSG00000273217 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1397310383 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60608,RMVar_hsa_circ_95431,RMVar_hsa_circ_123864,RMVar_hsa_circ_114349,RMVar_hsa_circ_119082,RMVar_hsa_circ_98414,RMVar_hsa_circ_234292,RMVar_hsa_circ_83654,RMVar_hsa_circ_93710,RMVar_hsa_circ_93850,RMVar_hsa_circ_91175,RMVar_hsa_circ_234296,RMVar_hsa_circ_76695,RMVar_hsa_circ_79178,RMVar_hsa_circ_234297,RMVar_hsa_circ_234294,RMVar_hsa_circ_234295,RMVar_hsa_circ_234293,RMVar_hsa_circ_234288,RMVar_hsa_circ_234290,RMVar_hsa_circ_234291,RMVar_hsa_circ_234289,RMVar_hsa_circ_127680,RMVar_hsa_circ_312259,RMVar_hsa_circ_234287,RMVar_hsa_circ_341545,RMVar_hsa_circ_234300,RMVar_hsa_circ_64913,RMVar_hsa_circ_234301,RMVar_hsa_circ_367832,RMVar_hsa_circ_290384,RMVar_hsa_circ_43505,RMVar_hsa_circ_55927,RMVar_hsa_circ_234303,RMVar_hsa_circ_234304 46877 RMVar_ID_46877 Human_SNP_ID_251579826 A-to-I Human chr5 - 131664417 131664417 131664417 TATCCAGGCTGGTCTCGAACTCTGGAGCCTCAAGTGATCCTCCCACCTCGGCCTCCCAAAAATCT TATCCAGGCTGGTCTCGAACTCTGGAGCCTCAGGTGATCCTCCCACCTCGGCCTCCCAAAAATCT T C FNIP1,AC008695.1 Ensembl:ENSG00000217128,Ensembl:ENSG00000273217 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1448180653 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60608,RMVar_hsa_circ_95431,RMVar_hsa_circ_123864,RMVar_hsa_circ_114349,RMVar_hsa_circ_119082,RMVar_hsa_circ_98414,RMVar_hsa_circ_234292,RMVar_hsa_circ_83654,RMVar_hsa_circ_93710,RMVar_hsa_circ_93850,RMVar_hsa_circ_91175,RMVar_hsa_circ_234296,RMVar_hsa_circ_76695,RMVar_hsa_circ_79178,RMVar_hsa_circ_234297,RMVar_hsa_circ_234294,RMVar_hsa_circ_234295,RMVar_hsa_circ_234293,RMVar_hsa_circ_234288,RMVar_hsa_circ_234290,RMVar_hsa_circ_234291,RMVar_hsa_circ_234289,RMVar_hsa_circ_127680,RMVar_hsa_circ_312259,RMVar_hsa_circ_234287,RMVar_hsa_circ_341545,RMVar_hsa_circ_234300,RMVar_hsa_circ_64913,RMVar_hsa_circ_234301,RMVar_hsa_circ_367832,RMVar_hsa_circ_290384,RMVar_hsa_circ_43505,RMVar_hsa_circ_55927,RMVar_hsa_circ_234303,RMVar_hsa_circ_234304 46878 RMVar_ID_46878 Human_SNP_ID_251580780 A-to-I Human chr5 - 131668451 131668451 131668451 GGAACTCCGACCTCAGGTGATCCACCCACCTCAGCCTCCCAAAGTGCTGGGATTATAGGCGTGAG GGAACTCCGACCTCAGGTGATCCACCCACCTCCGCCTCCCAAAGTGCTGGGATTATAGGCGTGAG T G FNIP1,AC008695.1 Ensembl:ENSG00000217128,Ensembl:ENSG00000273217 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355286494 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7380321 RMVar_hsa_circ_60608,RMVar_hsa_circ_95431,RMVar_hsa_circ_123864,RMVar_hsa_circ_114349,RMVar_hsa_circ_119082,RMVar_hsa_circ_98414,RMVar_hsa_circ_234292,RMVar_hsa_circ_83654,RMVar_hsa_circ_93710,RMVar_hsa_circ_93850,RMVar_hsa_circ_91175,RMVar_hsa_circ_234296,RMVar_hsa_circ_76695,RMVar_hsa_circ_79178,RMVar_hsa_circ_234297,RMVar_hsa_circ_234294,RMVar_hsa_circ_234295,RMVar_hsa_circ_234293,RMVar_hsa_circ_234288,RMVar_hsa_circ_234290,RMVar_hsa_circ_234291,RMVar_hsa_circ_234289,RMVar_hsa_circ_127680,RMVar_hsa_circ_312259,RMVar_hsa_circ_234287,RMVar_hsa_circ_341545,RMVar_hsa_circ_234300,RMVar_hsa_circ_64913,RMVar_hsa_circ_234301,RMVar_hsa_circ_367832,RMVar_hsa_circ_290384,RMVar_hsa_circ_43505,RMVar_hsa_circ_55927,RMVar_hsa_circ_234303,RMVar_hsa_circ_234304 46879 RMVar_ID_46879 Human_SNP_ID_251585110 A-to-I Human chr5 - 131687184 131687184 131687184 GGAGGATCAGTTGAACCTGGGATTCAGAGGTTACAGTGAGCCGAGATTGTGCCATTGCACTCTAG GGAGGATCAGTTGAACCTGGGATTCAGAGGTTGCAGTGAGCCGAGATTGTGCCATTGCACTCTAG T C FNIP1,AC008695.1 Ensembl:ENSG00000217128,Ensembl:ENSG00000273217 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs912560095 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15290588 RMVar_hsa_circ_60608,RMVar_hsa_circ_123864,RMVar_hsa_circ_114349,RMVar_hsa_circ_119082,RMVar_hsa_circ_98414,RMVar_hsa_circ_234292,RMVar_hsa_circ_83654,RMVar_hsa_circ_93850,RMVar_hsa_circ_76695,RMVar_hsa_circ_79178,RMVar_hsa_circ_234294,RMVar_hsa_circ_234293,RMVar_hsa_circ_234288,RMVar_hsa_circ_234290,RMVar_hsa_circ_234291,RMVar_hsa_circ_234289,RMVar_hsa_circ_127680,RMVar_hsa_circ_234287,RMVar_hsa_circ_341545,RMVar_hsa_circ_64913,RMVar_hsa_circ_234301,RMVar_hsa_circ_367832,RMVar_hsa_circ_64165,RMVar_hsa_circ_55927,RMVar_hsa_circ_234304,RMVar_hsa_circ_275435,RMVar_hsa_circ_331004,RMVar_hsa_circ_369168,RMVar_hsa_circ_358487,RMVar_hsa_circ_301999,RMVar_hsa_circ_304693,RMVar_hsa_circ_274954,RMVar_hsa_circ_99767,RMVar_hsa_circ_234308,RMVar_hsa_circ_234306,RMVar_hsa_circ_234307,RMVar_hsa_circ_234305,RMVar_hsa_circ_34829,RMVar_hsa_circ_234315,RMVar_hsa_circ_266743,RMVar_hsa_circ_289138,RMVar_hsa_circ_356711,RMVar_hsa_circ_301863,RMVar_hsa_circ_285745,RMVar_hsa_circ_60199,RMVar_hsa_circ_121732,RMVar_hsa_circ_234316,RMVar_hsa_circ_234317,RMVar_hsa_circ_234314,RMVar_hsa_circ_70043,RMVar_hsa_circ_234318 46880 RMVar_ID_46880 Human_SNP_ID_251587551 A-to-I Human chr5 - 131697375 131697375 131697375 TGTGCCTGTAATCCCAGTACTTTGGGAGGCCAAGGTGGTTAGATTGCTTGAGCTCAGGAGTTCGA TGTGCCTGTAATCCCAGTACTTTGGGAGGCCAGGGTGGTTAGATTGCTTGAGCTCAGGAGTTCGA T C FNIP1,AC008695.1 Ensembl:ENSG00000217128,Ensembl:ENSG00000273217 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs529446788 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60608,RMVar_hsa_circ_123864,RMVar_hsa_circ_114349,RMVar_hsa_circ_119082,RMVar_hsa_circ_98414,RMVar_hsa_circ_234292,RMVar_hsa_circ_83654,RMVar_hsa_circ_93850,RMVar_hsa_circ_76695,RMVar_hsa_circ_79178,RMVar_hsa_circ_234294,RMVar_hsa_circ_234293,RMVar_hsa_circ_234288,RMVar_hsa_circ_234290,RMVar_hsa_circ_234291,RMVar_hsa_circ_234289,RMVar_hsa_circ_127680,RMVar_hsa_circ_234287,RMVar_hsa_circ_341545,RMVar_hsa_circ_64913,RMVar_hsa_circ_234301,RMVar_hsa_circ_367832,RMVar_hsa_circ_64165,RMVar_hsa_circ_55927,RMVar_hsa_circ_234304,RMVar_hsa_circ_275435,RMVar_hsa_circ_331004,RMVar_hsa_circ_369168,RMVar_hsa_circ_358487,RMVar_hsa_circ_301999,RMVar_hsa_circ_304693,RMVar_hsa_circ_274954,RMVar_hsa_circ_99767,RMVar_hsa_circ_234308,RMVar_hsa_circ_234306,RMVar_hsa_circ_234307,RMVar_hsa_circ_234305,RMVar_hsa_circ_34829,RMVar_hsa_circ_234315,RMVar_hsa_circ_266743,RMVar_hsa_circ_289138,RMVar_hsa_circ_356711,RMVar_hsa_circ_301863,RMVar_hsa_circ_285745,RMVar_hsa_circ_60199,RMVar_hsa_circ_121732,RMVar_hsa_circ_234316,RMVar_hsa_circ_234317,RMVar_hsa_circ_234314,RMVar_hsa_circ_70043,RMVar_hsa_circ_234319,RMVar_hsa_circ_234321,RMVar_hsa_circ_234318,RMVar_hsa_circ_234320 46881 RMVar_ID_46881 Human_SNP_ID_251588164 A-to-I Human chr5 - 131699914 131699914 131699914 TATATTCCCTTTTTTTTTTTTTTTTTTTTTGAAACAGTCTTACTCCATCACCCAGGCTGGAGTGC TATATTCCCTTTTTTTTTTTTTTTTTTTTTGATACAGTCTTACTCCATCACCCAGGCTGGAGTGC T A FNIP1,AC008695.1 Ensembl:ENSG00000217128,Ensembl:ENSG00000273217 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1451706590 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60608,RMVar_hsa_circ_114349,RMVar_hsa_circ_119082,RMVar_hsa_circ_98414,RMVar_hsa_circ_234292,RMVar_hsa_circ_83654,RMVar_hsa_circ_93850,RMVar_hsa_circ_76695,RMVar_hsa_circ_79178,RMVar_hsa_circ_234293,RMVar_hsa_circ_234288,RMVar_hsa_circ_234290,RMVar_hsa_circ_234291,RMVar_hsa_circ_234289,RMVar_hsa_circ_127680,RMVar_hsa_circ_234287,RMVar_hsa_circ_341545,RMVar_hsa_circ_234301,RMVar_hsa_circ_64165,RMVar_hsa_circ_55927,RMVar_hsa_circ_275435,RMVar_hsa_circ_331004,RMVar_hsa_circ_369168,RMVar_hsa_circ_301999,RMVar_hsa_circ_304693,RMVar_hsa_circ_274954,RMVar_hsa_circ_99767,RMVar_hsa_circ_234306,RMVar_hsa_circ_234307,RMVar_hsa_circ_234305,RMVar_hsa_circ_34829,RMVar_hsa_circ_234315,RMVar_hsa_circ_266743,RMVar_hsa_circ_356711,RMVar_hsa_circ_301863,RMVar_hsa_circ_285745,RMVar_hsa_circ_60199,RMVar_hsa_circ_121732,RMVar_hsa_circ_234316,RMVar_hsa_circ_234317,RMVar_hsa_circ_70043,RMVar_hsa_circ_24051,RMVar_hsa_circ_234321,RMVar_hsa_circ_234320,RMVar_hsa_circ_285192,RMVar_hsa_circ_312642,RMVar_hsa_circ_333373,RMVar_hsa_circ_290371,RMVar_hsa_circ_51071,RMVar_hsa_circ_234323,RMVar_hsa_circ_7689,RMVar_hsa_circ_234324,RMVar_hsa_circ_234322 46882 RMVar_ID_46882 Human_SNP_ID_251588165 A-to-I Human chr5 - 131699914 131699914 131699914 TATATTCCCTTTTTTTTTTTTTTTTTTTTTGAAACAGTCTTACTCCATCACCCAGGCTGGAGTGC TATATTCCCTTTTTTTTTTTTTTTTTTTTTGAGACAGTCTTACTCCATCACCCAGGCTGGAGTGC T C FNIP1,AC008695.1 Ensembl:ENSG00000217128,Ensembl:ENSG00000273217 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1451706590 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60608,RMVar_hsa_circ_114349,RMVar_hsa_circ_119082,RMVar_hsa_circ_98414,RMVar_hsa_circ_234292,RMVar_hsa_circ_83654,RMVar_hsa_circ_93850,RMVar_hsa_circ_76695,RMVar_hsa_circ_79178,RMVar_hsa_circ_234293,RMVar_hsa_circ_234288,RMVar_hsa_circ_234290,RMVar_hsa_circ_234291,RMVar_hsa_circ_234289,RMVar_hsa_circ_127680,RMVar_hsa_circ_234287,RMVar_hsa_circ_341545,RMVar_hsa_circ_234301,RMVar_hsa_circ_64165,RMVar_hsa_circ_55927,RMVar_hsa_circ_275435,RMVar_hsa_circ_331004,RMVar_hsa_circ_369168,RMVar_hsa_circ_301999,RMVar_hsa_circ_304693,RMVar_hsa_circ_274954,RMVar_hsa_circ_99767,RMVar_hsa_circ_234306,RMVar_hsa_circ_234307,RMVar_hsa_circ_234305,RMVar_hsa_circ_34829,RMVar_hsa_circ_234315,RMVar_hsa_circ_266743,RMVar_hsa_circ_356711,RMVar_hsa_circ_301863,RMVar_hsa_circ_285745,RMVar_hsa_circ_60199,RMVar_hsa_circ_121732,RMVar_hsa_circ_234316,RMVar_hsa_circ_234317,RMVar_hsa_circ_70043,RMVar_hsa_circ_24051,RMVar_hsa_circ_234321,RMVar_hsa_circ_234320,RMVar_hsa_circ_285192,RMVar_hsa_circ_312642,RMVar_hsa_circ_333373,RMVar_hsa_circ_290371,RMVar_hsa_circ_51071,RMVar_hsa_circ_234323,RMVar_hsa_circ_7689,RMVar_hsa_circ_234324,RMVar_hsa_circ_234322 46883 RMVar_ID_46883 Human_SNP_ID_251590807 A-to-I Human chr5 - 131711639 131711639 131711639 GTTCTCAAAATTAGCTGGGCCTGGTGGCATGCACCTGTAGTCCTGGCTCATGGGGAGGGTTGAGG GTTCTCAAAATTAGCTGGGCCTGGTGGCATGCGCCTGTAGTCCTGGCTCATGGGGAGGGTTGAGG T C FNIP1,AC008695.1 Ensembl:ENSG00000217128,Ensembl:ENSG00000273217 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1449892859 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17575462 RMVar_hsa_circ_122,RMVar_hsa_circ_60608,RMVar_hsa_circ_114349,RMVar_hsa_circ_119082,RMVar_hsa_circ_83654,RMVar_hsa_circ_79178,RMVar_hsa_circ_234288,RMVar_hsa_circ_234290,RMVar_hsa_circ_234289,RMVar_hsa_circ_127680,RMVar_hsa_circ_234287,RMVar_hsa_circ_234301,RMVar_hsa_circ_64165,RMVar_hsa_circ_331004,RMVar_hsa_circ_369168,RMVar_hsa_circ_301999,RMVar_hsa_circ_304693,RMVar_hsa_circ_234306,RMVar_hsa_circ_234305,RMVar_hsa_circ_34829,RMVar_hsa_circ_266743,RMVar_hsa_circ_356711,RMVar_hsa_circ_60199,RMVar_hsa_circ_121732,RMVar_hsa_circ_234317,RMVar_hsa_circ_24051,RMVar_hsa_circ_234321,RMVar_hsa_circ_333373,RMVar_hsa_circ_290371,RMVar_hsa_circ_7689,RMVar_hsa_circ_234324,RMVar_hsa_circ_339038,RMVar_hsa_circ_370601,RMVar_hsa_circ_234325,RMVar_hsa_circ_318070,RMVar_hsa_circ_234326 46884 RMVar_ID_46884 Human_SNP_ID_251591675 A-to-I Human chr5 - 131715294 131715294 131715294 TTTAATAGAGACAGGGTTTTGATGTGTTGGCCAGGCTGTTCTCGAACTCCTGACCGCAGGTGATC TTTAATAGAGACAGGGTTTTGATGTGTTGGCCGGGCTGTTCTCGAACTCCTGACCGCAGGTGATC T C FNIP1,AC008695.1 Ensembl:ENSG00000217128,Ensembl:ENSG00000273217 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs552190656 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_630596 RMVar_hsa_circ_122,RMVar_hsa_circ_60608,RMVar_hsa_circ_114349,RMVar_hsa_circ_119082,RMVar_hsa_circ_83654,RMVar_hsa_circ_79178,RMVar_hsa_circ_234288,RMVar_hsa_circ_234290,RMVar_hsa_circ_234289,RMVar_hsa_circ_127680,RMVar_hsa_circ_234287,RMVar_hsa_circ_234301,RMVar_hsa_circ_64165,RMVar_hsa_circ_331004,RMVar_hsa_circ_369168,RMVar_hsa_circ_301999,RMVar_hsa_circ_304693,RMVar_hsa_circ_234306,RMVar_hsa_circ_234305,RMVar_hsa_circ_34829,RMVar_hsa_circ_266743,RMVar_hsa_circ_356711,RMVar_hsa_circ_60199,RMVar_hsa_circ_121732,RMVar_hsa_circ_234317,RMVar_hsa_circ_24051,RMVar_hsa_circ_234321,RMVar_hsa_circ_333373,RMVar_hsa_circ_290371,RMVar_hsa_circ_7689,RMVar_hsa_circ_234324,RMVar_hsa_circ_339038,RMVar_hsa_circ_370601,RMVar_hsa_circ_234325,RMVar_hsa_circ_318070,RMVar_hsa_circ_234326 46885 RMVar_ID_46885 Human_SNP_ID_251600077 A-to-I Human chr5 - 131749529 131749529 131749529 AAATTAGCCAGGCATGATGGCACACGCCTGTAAACCCAGCAACTGGGGAGGCTGAGGCAGGAGAA AAATTAGCCAGGCATGATGGCACACGCCTGTAGACCCAGCAACTGGGGAGGCTGAGGCAGGAGAA T C FNIP1,AC008695.1 Ensembl:ENSG00000217128,Ensembl:ENSG00000273217 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049145186 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79178,RMVar_hsa_circ_234287,RMVar_hsa_circ_121732,RMVar_hsa_circ_234317 46886 RMVar_ID_46886 Human_SNP_ID_251650086 A-to-I Human chr5 - 131951621 131951621 131951621 AGATCCCGCCACTGTACTCCAGCCTGGGCAACAGAACGAGACTCCGTCTCAAAAAGAAAGAAAAA AGATCCCGCCACTGTACTCCAGCCTGGGCAACCGAACGAGACTCCGTCTCAAAAAGAAAGAAAAA T G AC034228.3,ACSL6 Ensembl:ENSG00000281938,Ensembl:ENSG00000164398 Protein coding,Protein coding intron,3'UTR GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1174364439 Functional Loss SNV dbSNP153 33..33 33 - - - 46887 RMVar_ID_46887 Human_SNP_ID_251650087 A-to-I Human chr5 - 131951624 131951624 131951624 CCGAGATCCCGCCACTGTACTCCAGCCTGGGCAACAGAACGAGACTCCGTCTCAAAAAGAAAGAA CCGAGATCCCGCCACTGTACTCCAGCCTGGGCGACAGAACGAGACTCCGTCTCAAAAAGAAAGAA T C AC034228.3,ACSL6 Ensembl:ENSG00000281938,Ensembl:ENSG00000164398 Protein coding,Protein coding intron,3'UTR GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs568818106 Functional Loss SNV dbSNP153 33..33 33 - - - 46888 RMVar_ID_46888 Human_SNP_ID_251650432 A-to-I Human chr5 - 131953357 131953357 131953357 CTCCCGCCTTGGCCTCCCTAAGTGCTAGGATTACAGGCATGAGCCATTGTTCCCAGCCAAATTCA CTCCCGCCTTGGCCTCCCTAAGTGCTAGGATTTCAGGCATGAGCCATTGTTCCCAGCCAAATTCA T A AC034228.3,ACSL6 Ensembl:ENSG00000281938,Ensembl:ENSG00000164398 Protein coding,Protein coding intron,3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1015468109 Functional Loss SNV dbSNP153 33..33 33 - - - 46889 RMVar_ID_46889 Human_SNP_ID_251650463 A-to-I Human chr5 - 131953497 131953497 131953497 GGGCTCGAGTGATCCTCCTGTCTCACCTCCCAAGTAGCTGAGACTACAGTACAGGCACATGCCAC GGGCTCGAGTGATCCTCCTGTCTCACCTCCCAGGTAGCTGAGACTACAGTACAGGCACATGCCAC T C AC034228.3,ACSL6 Ensembl:ENSG00000281938,Ensembl:ENSG00000164398 Protein coding,Protein coding intron,3'UTR GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1416205004 Functional Loss SNV dbSNP153 33..33 33 - - - 46890 RMVar_ID_46890 Human_SNP_ID_251650467 A-to-I Human chr5 - 131953505 131953505 131953505 CATCTCCTGGGCTCGAGTGATCCTCCTGTCTCACCTCCCAAGTAGCTGAGACTACAGTACAGGCA CATCTCCTGGGCTCGAGTGATCCTCCTGTCTCTCCTCCCAAGTAGCTGAGACTACAGTACAGGCA T A AC034228.3,ACSL6 Ensembl:ENSG00000281938,Ensembl:ENSG00000164398 Protein coding,Protein coding intron,3'UTR GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1302572617 Functional Loss SNV dbSNP153 33..33 33 - - - 46891 RMVar_ID_46891 Human_SNP_ID_251739626 A-to-I Human chr5 - 132331150 132331150 132331150 TTTTGCATTTTTTGTAGAGACTGGGTTTCACCATGTTGGCCAGGTTGGTCTCAAACTCCTGGCCT TTTTGCATTTTTTGTAGAGACTGGGTTTCACCGTGTTGGCCAGGTTGGTCTCAAACTCCTGGCCT T C MIR3936HG Ensembl:ENSG00000233006 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs959028720 Functional Loss SNV dbSNP153 33..33 33 - - - 46892 RMVar_ID_46892 Human_SNP_ID_251739627 A-to-I Human chr5 - 132331150 132331150 132331150 TTTTGCATTTTTTGTAGAGACTGGGTTTCACCATGTTGGCCAGGTTGGTCTCAAACTCCTGGCCT TTTTGCATTTTTTGTAGAGACTGGGTTTCACCCTGTTGGCCAGGTTGGTCTCAAACTCCTGGCCT T G MIR3936HG Ensembl:ENSG00000233006 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs959028720 Functional Loss SNV dbSNP153 33..33 33 - - - 46893 RMVar_ID_46893 Human_SNP_ID_251739872 A-to-I Human chr5 - 132332273 132332272 132332273 GTCTTGCTCTGCTGCCCAGGCTGGAGTACAGTAGTGCGATCAAGGCTCACTGGAACCTCCACCTC GTCTTGCTCTGCTGCCCAGGCTGGAGTACAGT_GTGCGATCAAGGCTCACTGGAACCTCCACCTC CT C MIR3936HG Ensembl:ENSG00000233006 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1165799221 Functional Loss DEL dbSNP153 33..33 33 - - - Human_Splice_Rec_690420,Human_Splice_Rec_690421,Human_Splice_Rec_690426,Human_Splice_Rec_690427,Human_Splice_Rec_690436 46894 RMVar_ID_46894 Human_SNP_ID_251744274 A-to-I Human chr5 - 132351543 132351543 132351543 ATATAAGGCTGGGGCCGGGCACAGTGGCTCACACCTATAATCCCAGCACTTTGGGAGGCTGAGGC ATATAAGGCTGGGGCCGGGCACAGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCTGAGGC T C MIR3936HG Ensembl:ENSG00000233006 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1457100051 Functional Loss SNV dbSNP153 33..33 33 - - - 46895 RMVar_ID_46895 Human_SNP_ID_251744275 A-to-I Human chr5 - 132351543 132351543 132351543 ATATAAGGCTGGGGCCGGGCACAGTGGCTCACACCTATAATCCCAGCACTTTGGGAGGCTGAGGC ATATAAGGCTGGGGCCGGGCACAGTGGCTCACCCCTATAATCCCAGCACTTTGGGAGGCTGAGGC T G MIR3936HG Ensembl:ENSG00000233006 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1457100051 Functional Loss SNV dbSNP153 33..33 33 - - - 46896 RMVar_ID_46896 Human_SNP_ID_251744340 A-to-I Human chr5 + 132351750 132351750 132351750 GCTAACAGAATACAGGCAAGAAACTGGATTCTACATATGTTGAAATTATGGCAAAAGACTTTATT GCTAACAGAATACAGGCAAGAAACTGGATTCTGCATATGTTGAAATTATGGCAAAAGACTTTATT A G lnc-SLC22A5-1 RNACentral:URS00008B5099 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs201881418 Functional Loss SNV dbSNP153 33..33 33 - - - 46897 RMVar_ID_46897 Human_SNP_ID_251744363 A-to-I Human chr5 - 132351873 132351873 132351873 TAGAGCAACATGTGCTCCTAATTTCATCCCAAATCTGCTCTTCCTGAAGTCCTCCCCAACTCAGT TAGAGCAACATGTGCTCCTAATTTCATCCCAAGTCTGCTCTTCCTGAAGTCCTCCCCAACTCAGT T C MIR3936HG Ensembl:ENSG00000233006 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1035022220 Functional Loss SNV dbSNP153 33..33 33 - - - 46898 RMVar_ID_46898 Human_SNP_ID_251744364 A-to-I Human chr5 - 132351874 132351874 132351874 CTAGAGCAACATGTGCTCCTAATTTCATCCCAAATCTGCTCTTCCTGAAGTCCTCCCCAACTCAG CTAGAGCAACATGTGCTCCTAATTTCATCCCAGATCTGCTCTTCCTGAAGTCCTCCCCAACTCAG T C MIR3936HG Ensembl:ENSG00000233006 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1402182986 Functional Loss SNV dbSNP153 33..33 33 - - - 46899 RMVar_ID_46899 Human_SNP_ID_251744445 A-to-I Human chr5 - 132352386 132352386 132352386 GCTGGAGTGCAATGACACAATCTCGGCTCACTATAACCTCTGCCTTCTGGGTCCAAGTGTTTTTC GCTGGAGTGCAATGACACAATCTCGGCTCACTTTAACCTCTGCCTTCTGGGTCCAAGTGTTTTTC T A MIR3936HG Ensembl:ENSG00000233006 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs987215249 Functional Loss SNV dbSNP153 33..33 33 - - - 46900 RMVar_ID_46900 Human_SNP_ID_251744446 A-to-I Human chr5 - 132352386 132352386 132352386 GCTGGAGTGCAATGACACAATCTCGGCTCACTATAACCTCTGCCTTCTGGGTCCAAGTGTTTTTC GCTGGAGTGCAATGACACAATCTCGGCTCACTGTAACCTCTGCCTTCTGGGTCCAAGTGTTTTTC T C MIR3936HG Ensembl:ENSG00000233006 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs987215249 Functional Loss SNV dbSNP153 33..33 33 - - - 46901 RMVar_ID_46901 Human_SNP_ID_251744544 A-to-I Human chr5 - 132352879 132352879 132352879 GGAAGAAACTGGATTCTGCATATGTTGAAATTATGGCAAAAGATTTTATTGACAGATTGGATGTG GGAAGAAACTGGATTCTGCATATGTTGAAATTGTGGCAAAAGATTTTATTGACAGATTGGATGTG T C MIR3936HG Ensembl:ENSG00000233006 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs539637191 Functional Loss SNV dbSNP153 33..33 33 - - - 46902 RMVar_ID_46902 Human_SNP_ID_251744555 A-to-I Human chr5 - 132352909 132352909 132352909 AAGGATTGGCTGGGGGCTAACAGAATGCAGGGAAGAAACTGGATTCTGCATATGTTGAAATTATG AAGGATTGGCTGGGGGCTAACAGAATGCAGGGGAGAAACTGGATTCTGCATATGTTGAAATTATG T C MIR3936HG Ensembl:ENSG00000233006 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031866055 Functional Loss SNV dbSNP153 33..33 33 - - - 46903 RMVar_ID_46903 Human_SNP_ID_251744562 A-to-I Human chr5 - 132352922 132352922 132352922 AGCCTTAATGAAGAAGGATTGGCTGGGGGCTAACAGAATGCAGGGAAGAAACTGGATTCTGCATA AGCCTTAATGAAGAAGGATTGGCTGGGGGCTAGCAGAATGCAGGGAAGAAACTGGATTCTGCATA T C MIR3936HG Ensembl:ENSG00000233006 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1237273336 Functional Loss SNV dbSNP153 33..33 33 - - - 46904 RMVar_ID_46904 Human_SNP_ID_251744563 A-to-I Human chr5 - 132352923 132352923 132352923 CAGCCTTAATGAAGAAGGATTGGCTGGGGGCTAACAGAATGCAGGGAAGAAACTGGATTCTGCAT CAGCCTTAATGAAGAAGGATTGGCTGGGGGCTGACAGAATGCAGGGAAGAAACTGGATTCTGCAT T C MIR3936HG Ensembl:ENSG00000233006 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1314323291 Functional Loss SNV dbSNP153 33..33 33 - - - 46905 RMVar_ID_46905 Human_SNP_ID_251744573 A-to-I Human chr5 - 132352975 132352975 132352975 ATTGAGATATCCCTGACTACTATGCTGAGAGTAGATTGAAGGGGCGTAGGAGCAGCCTTAATGAA ATTGAGATATCCCTGACTACTATGCTGAGAGTGGATTGAAGGGGCGTAGGAGCAGCCTTAATGAA T C MIR3936HG Ensembl:ENSG00000233006 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1009189453 Functional Loss SNV dbSNP153 33..33 33 - - - 46906 RMVar_ID_46906 Human_SNP_ID_251744574 A-to-I Human chr5 - 132352980 132352980 132352980 ATGTGATTGAGATATCCCTGACTACTATGCTGAGAGTAGATTGAAGGGGCGTAGGAGCAGCCTTA ATGTGATTGAGATATCCCTGACTACTATGCTGGGAGTAGATTGAAGGGGCGTAGGAGCAGCCTTA T C MIR3936HG Ensembl:ENSG00000233006 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs995974596 Functional Loss SNV dbSNP153 33..33 33 - - - 46907 RMVar_ID_46907 Human_SNP_ID_251744576 A-to-I Human chr5 - 132352989 132352989 132352989 AGTAACATGATGTGATTGAGATATCCCTGACTACTATGCTGAGAGTAGATTGAAGGGGCGTAGGA AGTAACATGATGTGATTGAGATATCCCTGACTGCTATGCTGAGAGTAGATTGAAGGGGCGTAGGA T C MIR3936HG Ensembl:ENSG00000233006 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs555439657 Functional Loss SNV dbSNP153 33..33 33 - - - 46908 RMVar_ID_46908 Human_SNP_ID_251746356 A-to-I Human chr5 - 132360672 132360672 132360672 GAGATCGAGACCATCCTGGCTAACATGGTGAAACCCCGTCTCTACCAAAAATACAAAAAATTAGC GAGATCGAGACCATCCTGGCTAACATGGTGAACCCCCGTCTCTACCAAAAATACAAAAAATTAGC T G MIR3936HG Ensembl:ENSG00000233006 lincRNA intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1025069925 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_168693 46909 RMVar_ID_46909 Human_SNP_ID_251746379 A-to-I Human chr5 - 132360744 132360744 132360744 GGCTGGGTGCAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGCGGATCATG GGCTGGGTGCAGTGGCTCATGCCTGTAATCCCTGCACTTTGGGAGGCCGAGGCAGGCGGATCATG T A MIR3936HG Ensembl:ENSG00000233006 lincRNA intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1275750905 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_168693 46910 RMVar_ID_46910 Human_SNP_ID_251746913 A-to-I Human chr5 - 132363229 132363229 132363229 CCACACCTGGCTAATTTTTGTATTTTTTGTAGAGATGGGATTTTGCCATGTTGCCCAGGCTGGTC CCACACCTGGCTAATTTTTGTATTTTTTGTAGCGATGGGATTTTGCCATGTTGCCCAGGCTGGTC T G MIR3936HG Ensembl:ENSG00000233006 lincRNA intron GSE100210;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229 RNA-Seq:(High) rs1333991537 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15292514 46911 RMVar_ID_46911 Human_SNP_ID_251746926 A-to-I Human chr5 - 132363268 132363268 132363268 CTCACACCTCATCTTCCCCAGAAGCTAGGACTACACGCACCACACCTGGCTAATTTTTGTATTTT CTCACACCTCATCTTCCCCAGAAGCTAGGACTGCACGCACCACACCTGGCTAATTTTTGTATTTT T C MIR3936HG Ensembl:ENSG00000233006 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs530962079 Functional Loss SNV dbSNP153 33..33 33 - - - 46912 RMVar_ID_46912 Human_SNP_ID_251746929 A-to-I Human chr5 - 132363274 132363274 132363274 GTGATCCTCACACCTCATCTTCCCCAGAAGCTAGGACTACACGCACCACACCTGGCTAATTTTTG GTGATCCTCACACCTCATCTTCCCCAGAAGCTGGGACTACACGCACCACACCTGGCTAATTTTTG T C MIR3936HG Ensembl:ENSG00000233006 lincRNA intron GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 29129909,30559470 RNA-Seq:(High) rs1304848771 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5250576 46913 RMVar_ID_46913 Human_SNP_ID_251746940 A-to-I Human chr5 - 132363307 132363307 132363307 TGACTCTCTGCAACTTCTGCCTCCTGGGCTTAAGTGATCCTCACACCTCATCTTCCCCAGAAGCT TGACTCTCTGCAACTTCTGCCTCCTGGGCTTAGGTGATCCTCACACCTCATCTTCCCCAGAAGCT T C MIR3936HG Ensembl:ENSG00000233006 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042626188 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5250576 46914 RMVar_ID_46914 Human_SNP_ID_251746946 A-to-I Human chr5 - 132363346 132363346 132363346 TCTCACTGTCACCCAGGCTGGAGTGCAGTGGCATGATCTTGACTCTCTGCAACTTCTGCCTCCTG TCTCACTGTCACCCAGGCTGGAGTGCAGTGGCGTGATCTTGACTCTCTGCAACTTCTGCCTCCTG T C MIR3936HG Ensembl:ENSG00000233006 lincRNA intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs748306230 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5250576 46915 RMVar_ID_46915 Human_SNP_ID_251747272 A-to-I Human chr5 - 132365032 132365032 132365032 CCACCACCAGGCCCGGCTAATTTTTTGTATTTAGTAGAGTCAGGGTTTCCCCATGTTGGTCAGCC CCACCACCAGGCCCGGCTAATTTTTTGTATTTGGTAGAGTCAGGGTTTCCCCATGTTGGTCAGCC T C MIR3936HG Ensembl:ENSG00000233006 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1358637221 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2893663,Human_RBP_ID_15292537 Human_Splice_Rec_690413,Human_Splice_Rec_690445 46916 RMVar_ID_46916 Human_SNP_ID_251747327 A-to-I Human chr5 - 132365263 132365263 132365263 GGTTAAATGAAGGTTGCCTGGTGGAGGTTGCTAGGGGAAAGGTGTTAAGTAAAAATGTTATATAA GGTTAAATGAAGGTTGCCTGGTGGAGGTTGCTGGGGGAAAGGTGTTAAGTAAAAATGTTATATAA T C MIR3936HG Ensembl:ENSG00000233006 lincRNA intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1434421622 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9169173,Human_RBP_ID_17196224 46917 RMVar_ID_46917 Human_SNP_ID_251770749 A-to-I Human chr5 + 132470578 132470578 132470578 CAGGATGAGGCTTTCCTGACTTTCTCCCCTAGAGGACTGATGTTCTCTACTGGTACAGACCTTGT CAGGATGAGGCTTTCCTGACTTTCTCCCCTAGGGGACTGATGTTCTCTACTGGTACAGACCTTGT A G AC116366.3,IRF1-AS1 Ensembl:ENSG00000283782,Ensembl:ENSG00000197536 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs2706380 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122625,RMVar_hsa_circ_234347 46918 RMVar_ID_46918 Human_SNP_ID_251771156 A-to-I Human chr5 + 132472589 132472589 132472589 GAAATCCTGTCTCTACAAAAAATTAGCTGGGCATGGTGGTATGTACCTGTAGTCCCAGCTTCTCC GAAATCCTGTCTCTACAAAAAATTAGCTGGGCGTGGTGGTATGTACCTGTAGTCCCAGCTTCTCC A G AC116366.3,IRF1-AS1 Ensembl:ENSG00000283782,Ensembl:ENSG00000197536 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs911821359 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122625,RMVar_hsa_circ_234347 46919 RMVar_ID_46919 Human_SNP_ID_251807343 A-to-I Human chr5 + 132623335 132623335 132623335 ACCCCGTCTGTACTAAAAAAAATACAAAAATTAGCTGGCTGTAGTGGTGCACACCTGTAATGCCA ACCCCGTCTGTACTAAAAAAAATACAAAAATTGGCTGGCTGTAGTGGTGCACACCTGTAATGCCA A G AC116366.3,RAD50 Ensembl:ENSG00000283782,Ensembl:ENSG00000113522 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1389864982 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44403,RMVar_hsa_circ_42435,RMVar_hsa_circ_50223 46920 RMVar_ID_46920 Human_SNP_ID_251812798 A-to-I Human chr5 + 132645941 132645941 132645941 ATCCCATCTTTACATAAAATTTTTAAAAAATTAGCAAGGCATGGTGGTGCACACCTGTAGTCTCA ATCCCATCTTTACATAAAATTTTTAAAAAATTGGCAAGGCATGGTGGTGCACACCTGTAGTCTCA A G AC116366.3,RAD50 Ensembl:ENSG00000283782,Ensembl:ENSG00000113522 Protein coding,Protein coding 3'UTR,3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1133994 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18038161 46921 RMVar_ID_46921 Human_SNP_ID_251812803 A-to-I Human chr5 + 132645967 132645967 132645967 AAAATTAGCAAGGCATGGTGGTGCACACCTGTAGTCTCAGCTACTTGGCTGAGATAGGATCCCTG AAAATTAGCAAGGCATGGTGGTGCACACCTGTGGTCTCAGCTACTTGGCTGAGATAGGATCCCTG A G AC116366.3,RAD50 Ensembl:ENSG00000283782,Ensembl:ENSG00000113522 Protein coding,Protein coding 3'UTR,3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1133998 Functional Loss SNV dbSNP153 33..33 33 - - - 46922 RMVar_ID_46922 Human_SNP_ID_251825044 A-to-I Human chr5 - 132693737 132693737 132693737 GACTTTGTGATCCGCCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCACGCC GACTTTGTGATCCGCCCGCCTCAGCCTCCCAAGGTGCTGGGATTACAGGTGTGAGCCACCACGCC T C KIF3A Ensembl:ENSG00000131437 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1306551047 Functional Loss SNV dbSNP153 33..33 33 - - - 46923 RMVar_ID_46923 Human_SNP_ID_251825045 A-to-I Human chr5 - 132693738 132693738 132693738 TGACTTTGTGATCCGCCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCACGC TGACTTTGTGATCCGCCCGCCTCAGCCTCCCAGAGTGCTGGGATTACAGGTGTGAGCCACCACGC T C KIF3A Ensembl:ENSG00000131437 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs539442602 Functional Loss SNV dbSNP153 33..33 33 - - - 46924 RMVar_ID_46924 Human_SNP_ID_251825046 A-to-I Human chr5 - 132693739 132693739 132693739 CTGACTTTGTGATCCGCCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCACG CTGACTTTGTGATCCGCCCGCCTCAGCCTCCCGAAGTGCTGGGATTACAGGTGTGAGCCACCACG T C KIF3A Ensembl:ENSG00000131437 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs556161740 Functional Loss SNV dbSNP153 33..33 33 - - - 46925 RMVar_ID_46925 Human_SNP_ID_251825092 A-to-I Human chr5 - 132693859 132693859 132693859 CTCCTGCCTCAGCCTCTTGAGTAGCTGGGATTACAGGTTTGCGCCACCACACCCAGCTAATTTTT CTCCTGCCTCAGCCTCTTGAGTAGCTGGGATTGCAGGTTTGCGCCACCACACCCAGCTAATTTTT T C KIF3A Ensembl:ENSG00000131437 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1159583382 Functional Loss SNV dbSNP153 33..33 33 - - - 46926 RMVar_ID_46926 Human_SNP_ID_251825212 A-to-I Human chr5 - 132694283 132694283 132694283 CTGTCTCTTCAGCCTCCTGAGTTGCTGGAACTACAGCTGTATGCCATCATGCTCGGCTAATTTTT CTGTCTCTTCAGCCTCCTGAGTTGCTGGAACTGCAGCTGTATGCCATCATGCTCGGCTAATTTTT T C KIF3A Ensembl:ENSG00000131437 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs893267221 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15293964,Human_RBP_ID_18352780 46927 RMVar_ID_46927 Human_SNP_ID_251857445 A-to-I Human chr5 - 132823623 132823623 132823623 CCTGCACCAAACAACAGCATCCAGGGCAAGAAAGTGAGTGGAGAAGGGCTGGTGGAGGCTGGGGG CCTGCACCAAACAACAGCATCCAGGGCAAGAATGTGAGTGGAGAAGGGCTGGTGGAGGCTGGGGG T A SHROOM1 Ensembl:ENSG00000164403 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs745681976 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_691769,Human_Splice_Rec_691783,Human_Splice_Rec_691795,Human_Splice_Rec_691805,Human_Splice_Rec_691809 RMVar_hsa_circ_51031 46928 RMVar_ID_46928 Human_SNP_ID_251876474 A-to-I Human chr5 - 132900497 132900497 132900497 GGAGTGCAGTGATGGGATGTCGGCTCACTGCAACCTCCAGCTCCCGGGTTCAAGCAATTCTCCTC GGAGTGCAGTGATGGGATGTCGGCTCACTGCACCCTCCAGCTCCCGGGTTCAAGCAATTCTCCTC T G AFF4 Ensembl:ENSG00000072364 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1299120139 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99039,RMVar_hsa_circ_234392,RMVar_hsa_circ_60074,RMVar_hsa_circ_376944,RMVar_hsa_circ_80330,RMVar_hsa_circ_234399,RMVar_hsa_circ_364342,RMVar_hsa_circ_268115,RMVar_hsa_circ_70765,RMVar_hsa_circ_12042,RMVar_hsa_circ_268451,RMVar_hsa_circ_29131,RMVar_hsa_circ_56594,RMVar_hsa_circ_333686,RMVar_hsa_circ_14319,RMVar_hsa_circ_100344,RMVar_hsa_circ_69535,RMVar_hsa_circ_234406 46929 RMVar_ID_46929 Human_SNP_ID_251879388 A-to-I Human chr5 - 132912334 132912334 132912334 CAGTTTGTTATCTTTACTTTTTTTTGAGACAGAGTATTGCTCTGTCACCCAGGCTGGAGTGCAGT CAGTTTGTTATCTTTACTTTTTTTTGAGACAGGGTATTGCTCTGTCACCCAGGCTGGAGTGCAGT T C AFF4 Ensembl:ENSG00000072364 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355893207 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99039,RMVar_hsa_circ_234392,RMVar_hsa_circ_60074,RMVar_hsa_circ_80330,RMVar_hsa_circ_234399,RMVar_hsa_circ_268115,RMVar_hsa_circ_70765,RMVar_hsa_circ_268451,RMVar_hsa_circ_29131,RMVar_hsa_circ_69535,RMVar_hsa_circ_70682 46930 RMVar_ID_46930 Human_SNP_ID_251879408 A-to-I Human chr5 - 132912423 132912423 132912423 CCCGGAGGTCTTGGCTGCAGTGAGCCATCATCACTCCACTGCACTCCAGTCTGGGTGGTAGTGAG CCCGGAGGTCTTGGCTGCAGTGAGCCATCATCGCTCCACTGCACTCCAGTCTGGGTGGTAGTGAG T C AFF4 Ensembl:ENSG00000072364 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956292868 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10180797,Human_RBP_ID_15295491 RMVar_hsa_circ_99039,RMVar_hsa_circ_234392,RMVar_hsa_circ_60074,RMVar_hsa_circ_80330,RMVar_hsa_circ_234399,RMVar_hsa_circ_268115,RMVar_hsa_circ_70765,RMVar_hsa_circ_268451,RMVar_hsa_circ_29131,RMVar_hsa_circ_69535,RMVar_hsa_circ_70682 46931 RMVar_ID_46931 Human_SNP_ID_251879711 A-to-I Human chr5 - 132913582 132913582 132913582 AAAATCAGCCGGGCACGGTGGTGGGCACCTGCAGTTGCAACTACTCAGGAGGCTGAAACAAGAGG AAAATCAGCCGGGCACGGTGGTGGGCACCTGCGGTTGCAACTACTCAGGAGGCTGAAACAAGAGG T C AFF4 Ensembl:ENSG00000072364 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs888030672 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99039,RMVar_hsa_circ_234392,RMVar_hsa_circ_60074,RMVar_hsa_circ_80330,RMVar_hsa_circ_234399,RMVar_hsa_circ_268115,RMVar_hsa_circ_70765,RMVar_hsa_circ_268451,RMVar_hsa_circ_29131,RMVar_hsa_circ_69535,RMVar_hsa_circ_70682 46932 RMVar_ID_46932 Human_SNP_ID_251879742 A-to-I Human chr5 - 132913708 132913708 132913708 AGCCAGTGTGGTGGCACACGCTTGTAATCCCAACACTTTAGAAGGCTGAGGTGGGAGGATCCCTG AGCCAGTGTGGTGGCACACGCTTGTAATCCCAGCACTTTAGAAGGCTGAGGTGGGAGGATCCCTG T C AFF4 Ensembl:ENSG00000072364 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1278520019 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99039,RMVar_hsa_circ_234392,RMVar_hsa_circ_60074,RMVar_hsa_circ_80330,RMVar_hsa_circ_234399,RMVar_hsa_circ_268115,RMVar_hsa_circ_70765,RMVar_hsa_circ_268451,RMVar_hsa_circ_29131,RMVar_hsa_circ_69535,RMVar_hsa_circ_70682 46933 RMVar_ID_46933 Human_SNP_ID_251880392 A-to-I Human chr5 - 132916190 132916190 132916190 CTGTCACCCAGGCTAGAGTGCAGTGGCATGATATCAGCTCATTGCAACCTCCGCTTCCCAAGCTC CTGTCACCCAGGCTAGAGTGCAGTGGCATGATGTCAGCTCATTGCAACCTCCGCTTCCCAAGCTC T C AFF4 Ensembl:ENSG00000072364 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1173410298 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99039,RMVar_hsa_circ_234392,RMVar_hsa_circ_60074,RMVar_hsa_circ_80330,RMVar_hsa_circ_234399,RMVar_hsa_circ_268115,RMVar_hsa_circ_70765,RMVar_hsa_circ_268451,RMVar_hsa_circ_29131,RMVar_hsa_circ_69535,RMVar_hsa_circ_70682 46934 RMVar_ID_46934 Human_SNP_ID_251881007 A-to-I Human chr5 - 132918196 132918196 132918196 TAAAGATGGCTTTTCACCATGTTGGCCAGGATAGTCTCGAACTCCTGGCCTCAAGTGGTCTGCCC TAAAGATGGCTTTTCACCATGTTGGCCAGGATGGTCTCGAACTCCTGGCCTCAAGTGGTCTGCCC T C AFF4 Ensembl:ENSG00000072364 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1323360310 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99039,RMVar_hsa_circ_234392,RMVar_hsa_circ_60074,RMVar_hsa_circ_80330,RMVar_hsa_circ_234399,RMVar_hsa_circ_268115,RMVar_hsa_circ_70765,RMVar_hsa_circ_268451,RMVar_hsa_circ_29131,RMVar_hsa_circ_69535,RMVar_hsa_circ_70682 46935 RMVar_ID_46935 Human_SNP_ID_251881220 A-to-I Human chr5 - 132919005 132919005 132919005 ATGGTGGTGCACACCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGTCTCTGGGAGGCAGA ATGGTGGTGCACACCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGTCTCTGGGAGGCAGA T C AFF4 Ensembl:ENSG00000072364 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs187926348 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99039,RMVar_hsa_circ_234392,RMVar_hsa_circ_60074,RMVar_hsa_circ_80330,RMVar_hsa_circ_234399,RMVar_hsa_circ_268115,RMVar_hsa_circ_70765,RMVar_hsa_circ_268451,RMVar_hsa_circ_29131,RMVar_hsa_circ_69535,RMVar_hsa_circ_70682 46936 RMVar_ID_46936 Human_SNP_ID_251881239 A-to-I Human chr5 - 132919061 132919061 132919061 CAACATGGTGAAACCCCGTCTCTACTAAAAACACAAAAATTAGTTGGGCACGGGGCATGGTGGTG CAACATGGTGAAACCCCGTCTCTACTAAAAACGCAAAAATTAGTTGGGCACGGGGCATGGTGGTG T C AFF4 Ensembl:ENSG00000072364 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1404513058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25853952 RMVar_hsa_circ_99039,RMVar_hsa_circ_234392,RMVar_hsa_circ_60074,RMVar_hsa_circ_80330,RMVar_hsa_circ_234399,RMVar_hsa_circ_268115,RMVar_hsa_circ_70765,RMVar_hsa_circ_268451,RMVar_hsa_circ_29131,RMVar_hsa_circ_69535,RMVar_hsa_circ_70682 46937 RMVar_ID_46937 Human_SNP_ID_251881392 A-to-I Human chr5 - 132919728 132919728 132919728 CTCATGCCTTGGTCTCCCGAATAGCTGGAATTACAAGTGCATGCCACCACACCCGGCTAATTTTT CTCATGCCTTGGTCTCCCGAATAGCTGGAATTGCAAGTGCATGCCACCACACCCGGCTAATTTTT T C AFF4 Ensembl:ENSG00000072364 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1389156603 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99039,RMVar_hsa_circ_234392,RMVar_hsa_circ_60074,RMVar_hsa_circ_80330,RMVar_hsa_circ_234399,RMVar_hsa_circ_268115,RMVar_hsa_circ_70765,RMVar_hsa_circ_268451,RMVar_hsa_circ_29131,RMVar_hsa_circ_69535,RMVar_hsa_circ_70682 46938 RMVar_ID_46938 Human_SNP_ID_251881528 A-to-I Human chr5 - 132920329 132920329 132920329 AAAAATGTTTGCCCGCTGGGCTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGT AAAAATGTTTGCCCGCTGGGCTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGT T C AFF4 Ensembl:ENSG00000072364 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170907446 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99039,RMVar_hsa_circ_234392,RMVar_hsa_circ_60074,RMVar_hsa_circ_80330,RMVar_hsa_circ_234399,RMVar_hsa_circ_268115,RMVar_hsa_circ_70765,RMVar_hsa_circ_268451,RMVar_hsa_circ_29131,RMVar_hsa_circ_69535,RMVar_hsa_circ_70682 46939 RMVar_ID_46939 Human_SNP_ID_251882122 A-to-I Human chr5 - 132922387 132922387 132922387 CTTTTTAAGACAAGGTCTCTGTTGTCCAGGCTAGAGTGCAGTGGCATGATCATGGCTCATTGCAC CTTTTTAAGACAAGGTCTCTGTTGTCCAGGCTGGAGTGCAGTGGCATGATCATGGCTCATTGCAC T C AFF4 Ensembl:ENSG00000072364 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404868862 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15558524,Human_RBP_ID_17575306 RMVar_hsa_circ_99039,RMVar_hsa_circ_234392,RMVar_hsa_circ_60074,RMVar_hsa_circ_80330,RMVar_hsa_circ_234399,RMVar_hsa_circ_268115,RMVar_hsa_circ_70765,RMVar_hsa_circ_268451,RMVar_hsa_circ_29131,RMVar_hsa_circ_69535,RMVar_hsa_circ_70682 46940 RMVar_ID_46940 Human_SNP_ID_251883409 A-to-I Human chr5 - 132927064 132927064 132927064 ATAATGTAAGAAAACTCTAAATGGCTTGACTAAAATCATATGGATTAAAAATTGTCTTGCCATTC ATAATGTAAGAAAACTCTAAATGGCTTGACTAGAATCATATGGATTAAAAATTGTCTTGCCATTC T C AFF4 Ensembl:ENSG00000072364 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1453806373 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99039,RMVar_hsa_circ_234392,RMVar_hsa_circ_60074,RMVar_hsa_circ_80330,RMVar_hsa_circ_234399,RMVar_hsa_circ_268115,RMVar_hsa_circ_70765,RMVar_hsa_circ_268451,RMVar_hsa_circ_29131,RMVar_hsa_circ_69535,RMVar_hsa_circ_70682 46941 RMVar_ID_46941 Human_SNP_ID_251887166 A-to-I Human chr5 - 132940870 132940870 132940870 GGCACCTGCCACCATGCCTGGCTAATTTTTGTATTTTTGGTGGAGATGGGGTTTCACCGTGTTGG GGCACCTGCCACCATGCCTGGCTAATTTTTGTGTTTTTGGTGGAGATGGGGTTTCACCGTGTTGG T C AFF4 Ensembl:ENSG00000072364 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1045096440 Functional Loss SNV dbSNP153 33..33 33 - - - 46942 RMVar_ID_46942 Human_SNP_ID_251887167 A-to-I Human chr5 - 132940879 132940879 132940879 GGGATTACAGGCACCTGCCACCATGCCTGGCTAATTTTTGTATTTTTGGTGGAGATGGGGTTTCA GGGATTACAGGCACCTGCCACCATGCCTGGCTGATTTTTGTATTTTTGGTGGAGATGGGGTTTCA T C AFF4 Ensembl:ENSG00000072364 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1262002308 Functional Loss SNV dbSNP153 33..33 33 - - - 46943 RMVar_ID_46943 Human_SNP_ID_251887366 A-to-I Human chr5 - 132941627 132941627 132941627 ATTGTGTGAGAAACTGAGTTTGTTGGCTGGGCACTGTGGCTCACACCTGTAATCCCAGCACATTT ATTGTGTGAGAAACTGAGTTTGTTGGCTGGGCGCTGTGGCTCACACCTGTAATCCCAGCACATTT T C AFF4 Ensembl:ENSG00000072364 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1254887555 Functional Loss SNV dbSNP153 33..33 33 - - - 46944 RMVar_ID_46944 Human_SNP_ID_251890089 A-to-I Human chr5 - 132951109 132951109 132951109 GCGATTCTCCTGCTTCAGCTTCCTGAGTAGCTAGGACTACAGGTTTGCACCACCACGCCTGGCTA GCGATTCTCCTGCTTCAGCTTCCTGAGTAGCTGGGACTACAGGTTTGCACCACCACGCCTGGCTA T C AFF4 Ensembl:ENSG00000072364 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1415660289 Functional Loss SNV dbSNP153 33..33 33 - - - 46945 RMVar_ID_46945 Human_SNP_ID_251892308 A-to-I Human chr5 - 132959222 132959222 132959222 ACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAACCTGGGAGGCGGAGGTTGCAGTGAGCTGAGAT ACTTGGGAGGCTGAGGCAGGAGAATCGCTTGATCCTGGGAGGCGGAGGTTGCAGTGAGCTGAGAT T A AFF4 Ensembl:ENSG00000072364 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1048973979 Functional Loss SNV dbSNP153 33..33 33 - - - 46946 RMVar_ID_46946 Human_SNP_ID_251892540 A-to-I Human chr5 - 132959857 132959857 132959857 GGGAGGCTGAGGCAGCAGAATGGCGTGAACCCAGGAGGCGGAGCTTGCAGTGAGTCGAGATCGCA GGGAGGCTGAGGCAGCAGAATGGCGTGAACCCGGGAGGCGGAGCTTGCAGTGAGTCGAGATCGCA T C AFF4 Ensembl:ENSG00000072364 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs894392466 Functional Loss SNV dbSNP153 33..33 33 - - - 46947 RMVar_ID_46947 Human_SNP_ID_251892568 A-to-I Human chr5 - 132959947 132959947 132959947 ATCGAGACCATCCTGGCTAACACGTCTCTACTAAAAGAATACAAAAAATTAGCTGGGTGTGGTGG ATCGAGACCATCCTGGCTAACACGTCTCTACTGAAAGAATACAAAAAATTAGCTGGGTGTGGTGG T C AFF4 Ensembl:ENSG00000072364 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1211744020 Functional Loss SNV dbSNP153 33..33 33 - - - 46948 RMVar_ID_46948 Human_SNP_ID_251892593 A-to-I Human chr5 - 132960036 132960036 132960036 AAAGCGCTCCTACTGGCCAGGCGCAGTGGCTTATGCCTGTAATCCCAGCACTTTGGGAGGCTGAG AAAGCGCTCCTACTGGCCAGGCGCAGTGGCTTGTGCCTGTAATCCCAGCACTTTGGGAGGCTGAG T C AFF4 Ensembl:ENSG00000072364 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1249576790 Functional Loss SNV dbSNP153 33..33 33 - - - 46949 RMVar_ID_46949 Human_SNP_ID_251892855 A-to-I Human chr5 - 132961010 132961010 132961010 AGCAGGTTGGTCAGACTGGTCTCGAACTCCTGACCTCGTGATCCACACGCCTCGGCCTCCCCAAA AGCAGGTTGGTCAGACTGGTCTCGAACTCCTGGCCTCGTGATCCACACGCCTCGGCCTCCCCAAA T C AFF4 Ensembl:ENSG00000072364 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956166443 Functional Loss SNV dbSNP153 33..33 33 - - - 46950 RMVar_ID_46950 Human_SNP_ID_251892932 A-to-I Human chr5 - 132961273 132961273 132961273 TGGTGGTACATGCCTGTAGTCCCAGCTACTCCAGAGGCTGAGGCACGAGAATCGCTTGAGAATCG TGGTGGTACATGCCTGTAGTCCCAGCTACTCCGGAGGCTGAGGCACGAGAATCGCTTGAGAATCG T C AFF4 Ensembl:ENSG00000072364 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs747271110 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17575473 46951 RMVar_ID_46951 Human_SNP_ID_251892934 A-to-I Human chr5 - 132961278 132961278 132961278 AGACATGGTGGTACATGCCTGTAGTCCCAGCTACTCCAGAGGCTGAGGCACGAGAATCGCTTGAG AGACATGGTGGTACATGCCTGTAGTCCCAGCTGCTCCAGAGGCTGAGGCACGAGAATCGCTTGAG T C AFF4 Ensembl:ENSG00000072364 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1225123932 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17575473 46952 RMVar_ID_46952 Human_SNP_ID_251892935 A-to-I Human chr5 - 132961278 132961278 132961278 AGACATGGTGGTACATGCCTGTAGTCCCAGCTACTCCAGAGGCTGAGGCACGAGAATCGCTTGAG AGACATGGTGGTACATGCCTGTAGTCCCAGCTCCTCCAGAGGCTGAGGCACGAGAATCGCTTGAG T G AFF4 Ensembl:ENSG00000072364 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1225123932 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17575473 46953 RMVar_ID_46953 Human_SNP_ID_251903188 A-to-I Human chr5 - 133000787 133000785 133000787 AATGTAAAAATTAGCCGGGCTTGGTGACACACACCTGTAGTCCCAGCTACTCAGGAGGCTGAGGC AATGTAAAAATTAGCCGGGCTTGGTGACACAC__CTGTAGTCCCAGCTACTCAGGAGGCTGAGGC GGT G ZCCHC10 Ensembl:ENSG00000155329 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1206294371 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_346860 46954 RMVar_ID_46954 Human_SNP_ID_251905303 A-to-I Human chr5 - 133008986 133008986 133008986 AAAAAAAAAAGAGAATCTCCCTCTGTCACCCAAGTTGAAGTGCAGTGGTGCAATCATAGCTTACT AAAAAAAAAAGAGAATCTCCCTCTGTCACCCATGTTGAAGTGCAGTGGTGCAATCATAGCTTACT T A ZCCHC10 Ensembl:ENSG00000155329 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388804795 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_234415,RMVar_hsa_circ_275936 46955 RMVar_ID_46955 Human_SNP_ID_251905304 A-to-I Human chr5 - 133008986 133008986 133008986 AAAAAAAAAAGAGAATCTCCCTCTGTCACCCAAGTTGAAGTGCAGTGGTGCAATCATAGCTTACT AAAAAAAAAAGAGAATCTCCCTCTGTCACCCAGGTTGAAGTGCAGTGGTGCAATCATAGCTTACT T C ZCCHC10 Ensembl:ENSG00000155329 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388804795 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_234415,RMVar_hsa_circ_275936 46956 RMVar_ID_46956 Human_SNP_ID_251906079 A-to-I Human chr5 - 133011911 133011911 133011911 TGCCCACACTGGTCTCGAACTTCTGACCTCAAATGATCTGCCTACCTTGGCCTCCCAGAGCGCTG TGCCCACACTGGTCTCGAACTTCTGACCTCAAGTGATCTGCCTACCTTGGCCTCCCAGAGCGCTG T C ZCCHC10 Ensembl:ENSG00000155329 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1451385165 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_234415,RMVar_hsa_circ_275936 46957 RMVar_ID_46957 Human_SNP_ID_251917954 A-to-I Human chr5 + 133053928 133053928 133053928 GTGATCCTCCCGCCTCGGCCTCCCAAAGTGCTAGGATTACAGGCGTGAGTCACGGTGCCCGGCCC GTGATCCTCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGTCACGGTGCCCGGCCC A G HSPA4 Ensembl:ENSG00000170606 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1262814591 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_234416,RMVar_hsa_circ_88039,RMVar_hsa_circ_124578,RMVar_hsa_circ_234417 46958 RMVar_ID_46958 Human_SNP_ID_251923992 A-to-I Human chr5 + 133075573 133075573 133075573 CAAAAGTTAGCTGGGTGTGGCGGTGTGCTTGTAGTCCTAGCTACTCTGGAGGCTGAGGTGGGGGG CAAAAGTTAGCTGGGTGTGGCGGTGTGCTTGTGGTCCTAGCTACTCTGGAGGCTGAGGTGGGGGG A G HSPA4 Ensembl:ENSG00000170606 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1440084474 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_838975,Human_RBP_ID_17159093 RMVar_hsa_circ_70160,RMVar_hsa_circ_234416,RMVar_hsa_circ_88039,RMVar_hsa_circ_124578,RMVar_hsa_circ_234417,RMVar_hsa_circ_288872,RMVar_hsa_circ_375351,RMVar_hsa_circ_374320,RMVar_hsa_circ_121056,RMVar_hsa_circ_96684,RMVar_hsa_circ_33747,RMVar_hsa_circ_234419,RMVar_hsa_circ_42618,RMVar_hsa_circ_51087,RMVar_hsa_circ_32623,RMVar_hsa_circ_234421,RMVar_hsa_circ_234422,RMVar_hsa_circ_234420,RMVar_hsa_circ_90522,RMVar_hsa_circ_234418,RMVar_hsa_circ_338073,RMVar_hsa_circ_65305,RMVar_hsa_circ_71595,RMVar_hsa_circ_234428,RMVar_hsa_circ_234429,RMVar_hsa_circ_269349,RMVar_hsa_circ_126922,RMVar_hsa_circ_62153,RMVar_hsa_circ_76295,RMVar_hsa_circ_123040,RMVar_hsa_circ_234430,RMVar_hsa_circ_234431,RMVar_hsa_circ_286846,RMVar_hsa_circ_234433,RMVar_hsa_circ_106211,RMVar_hsa_circ_234434,RMVar_hsa_circ_234435 46959 RMVar_ID_46959 Human_SNP_ID_251924429 A-to-I Human chr5 + 133077302 133077302 133077302 GCTGTTTTGCCCAGGCTGGAGTAAAGTGGCACAATCTCAACTCACTGCAACCTCCACCCCCAGGT GCTGTTTTGCCCAGGCTGGAGTAAAGTGGCACCATCTCAACTCACTGCAACCTCCACCCCCAGGT A C HSPA4 Ensembl:ENSG00000170606 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1253321818 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15296876 RMVar_hsa_circ_70160,RMVar_hsa_circ_234416,RMVar_hsa_circ_88039,RMVar_hsa_circ_124578,RMVar_hsa_circ_234417,RMVar_hsa_circ_375351,RMVar_hsa_circ_374320,RMVar_hsa_circ_121056,RMVar_hsa_circ_96684,RMVar_hsa_circ_33747,RMVar_hsa_circ_234419,RMVar_hsa_circ_42618,RMVar_hsa_circ_51087,RMVar_hsa_circ_32623,RMVar_hsa_circ_234421,RMVar_hsa_circ_234420,RMVar_hsa_circ_90522,RMVar_hsa_circ_234418,RMVar_hsa_circ_65305,RMVar_hsa_circ_71595,RMVar_hsa_circ_234429,RMVar_hsa_circ_269349,RMVar_hsa_circ_126922,RMVar_hsa_circ_76295,RMVar_hsa_circ_123040,RMVar_hsa_circ_234430,RMVar_hsa_circ_234431,RMVar_hsa_circ_234433,RMVar_hsa_circ_106211,RMVar_hsa_circ_36844,RMVar_hsa_circ_234434,RMVar_hsa_circ_234435,RMVar_hsa_circ_337012 46960 RMVar_ID_46960 Human_SNP_ID_251924656 A-to-I Human chr5 + 133078193 133078193 133078193 TCTCTACTAAAAATACAAGAAATTAGCCGGGTATGGTGGCGGGTGCCTGTAGTCCCAGCTGCTGG TCTCTACTAAAAATACAAGAAATTAGCCGGGTGTGGTGGCGGGTGCCTGTAGTCCCAGCTGCTGG A G HSPA4 Ensembl:ENSG00000170606 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1033055646 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70160,RMVar_hsa_circ_234416,RMVar_hsa_circ_88039,RMVar_hsa_circ_124578,RMVar_hsa_circ_234417,RMVar_hsa_circ_375351,RMVar_hsa_circ_374320,RMVar_hsa_circ_121056,RMVar_hsa_circ_96684,RMVar_hsa_circ_33747,RMVar_hsa_circ_234419,RMVar_hsa_circ_42618,RMVar_hsa_circ_51087,RMVar_hsa_circ_32623,RMVar_hsa_circ_234421,RMVar_hsa_circ_234420,RMVar_hsa_circ_90522,RMVar_hsa_circ_234418,RMVar_hsa_circ_65305,RMVar_hsa_circ_71595,RMVar_hsa_circ_234429,RMVar_hsa_circ_269349,RMVar_hsa_circ_126922,RMVar_hsa_circ_76295,RMVar_hsa_circ_123040,RMVar_hsa_circ_234430,RMVar_hsa_circ_234431,RMVar_hsa_circ_234433,RMVar_hsa_circ_106211,RMVar_hsa_circ_36844,RMVar_hsa_circ_234434,RMVar_hsa_circ_234435,RMVar_hsa_circ_337012 46961 RMVar_ID_46961 Human_SNP_ID_251924884 A-to-I Human chr5 + 133078873 133078873 133078873 CTCCTGCCTCAGTCTCCTGAGTAGCTGGGACTACAGGCACGTGCCACCACGCCTGGCTAATTTTT CTCCTGCCTCAGTCTCCTGAGTAGCTGGGACTGCAGGCACGTGCCACCACGCCTGGCTAATTTTT A G HSPA4 Ensembl:ENSG00000170606 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1187974048 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70160,RMVar_hsa_circ_234416,RMVar_hsa_circ_88039,RMVar_hsa_circ_124578,RMVar_hsa_circ_234417,RMVar_hsa_circ_375351,RMVar_hsa_circ_374320,RMVar_hsa_circ_121056,RMVar_hsa_circ_96684,RMVar_hsa_circ_33747,RMVar_hsa_circ_234419,RMVar_hsa_circ_42618,RMVar_hsa_circ_51087,RMVar_hsa_circ_32623,RMVar_hsa_circ_234421,RMVar_hsa_circ_234420,RMVar_hsa_circ_90522,RMVar_hsa_circ_234418,RMVar_hsa_circ_65305,RMVar_hsa_circ_71595,RMVar_hsa_circ_234429,RMVar_hsa_circ_269349,RMVar_hsa_circ_126922,RMVar_hsa_circ_76295,RMVar_hsa_circ_123040,RMVar_hsa_circ_234430,RMVar_hsa_circ_234431,RMVar_hsa_circ_234433,RMVar_hsa_circ_106211,RMVar_hsa_circ_36844,RMVar_hsa_circ_234434,RMVar_hsa_circ_234435,RMVar_hsa_circ_337012 46962 RMVar_ID_46962 Human_SNP_ID_251924887 A-to-I Human chr5 + 133078879 133078879 133078879 CCTCAGTCTCCTGAGTAGCTGGGACTACAGGCACGTGCCACCACGCCTGGCTAATTTTTGTATTT CCTCAGTCTCCTGAGTAGCTGGGACTACAGGCGCGTGCCACCACGCCTGGCTAATTTTTGTATTT A G HSPA4 Ensembl:ENSG00000170606 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1056135454 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70160,RMVar_hsa_circ_234416,RMVar_hsa_circ_88039,RMVar_hsa_circ_124578,RMVar_hsa_circ_234417,RMVar_hsa_circ_375351,RMVar_hsa_circ_374320,RMVar_hsa_circ_121056,RMVar_hsa_circ_96684,RMVar_hsa_circ_33747,RMVar_hsa_circ_234419,RMVar_hsa_circ_42618,RMVar_hsa_circ_51087,RMVar_hsa_circ_32623,RMVar_hsa_circ_234421,RMVar_hsa_circ_234420,RMVar_hsa_circ_90522,RMVar_hsa_circ_234418,RMVar_hsa_circ_65305,RMVar_hsa_circ_71595,RMVar_hsa_circ_234429,RMVar_hsa_circ_269349,RMVar_hsa_circ_126922,RMVar_hsa_circ_76295,RMVar_hsa_circ_123040,RMVar_hsa_circ_234430,RMVar_hsa_circ_234431,RMVar_hsa_circ_234433,RMVar_hsa_circ_106211,RMVar_hsa_circ_36844,RMVar_hsa_circ_234434,RMVar_hsa_circ_234435,RMVar_hsa_circ_337012 46963 RMVar_ID_46963 Human_SNP_ID_251924904 A-to-I Human chr5 + 133078917 133078917 133078917 CACCACGCCTGGCTAATTTTTGTATTTTTTGTAGAGACTGGGTGTCACCATGTTGCCCAGGCTGG CACCACGCCTGGCTAATTTTTGTATTTTTTGTGGAGACTGGGTGTCACCATGTTGCCCAGGCTGG A G HSPA4 Ensembl:ENSG00000170606 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1295340268 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70160,RMVar_hsa_circ_234416,RMVar_hsa_circ_88039,RMVar_hsa_circ_124578,RMVar_hsa_circ_234417,RMVar_hsa_circ_375351,RMVar_hsa_circ_374320,RMVar_hsa_circ_121056,RMVar_hsa_circ_96684,RMVar_hsa_circ_33747,RMVar_hsa_circ_234419,RMVar_hsa_circ_42618,RMVar_hsa_circ_51087,RMVar_hsa_circ_32623,RMVar_hsa_circ_234421,RMVar_hsa_circ_234420,RMVar_hsa_circ_90522,RMVar_hsa_circ_234418,RMVar_hsa_circ_65305,RMVar_hsa_circ_71595,RMVar_hsa_circ_234429,RMVar_hsa_circ_269349,RMVar_hsa_circ_126922,RMVar_hsa_circ_76295,RMVar_hsa_circ_123040,RMVar_hsa_circ_234430,RMVar_hsa_circ_234431,RMVar_hsa_circ_234433,RMVar_hsa_circ_106211,RMVar_hsa_circ_36844,RMVar_hsa_circ_234434,RMVar_hsa_circ_234435,RMVar_hsa_circ_337012 46964 RMVar_ID_46964 Human_SNP_ID_251925847 A-to-I Human chr5 + 133082666 133082666 133082666 TTTTGTATTTTTTGTAGAGACAGGATTTTGCCATATTGCTCAGGCTGGTCTCAGATTCCTGAGCT TTTTGTATTTTTTGTAGAGACAGGATTTTGCCCTATTGCTCAGGCTGGTCTCAGATTCCTGAGCT A C HSPA4 Ensembl:ENSG00000170606 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1470100509 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70160,RMVar_hsa_circ_234416,RMVar_hsa_circ_88039,RMVar_hsa_circ_124578,RMVar_hsa_circ_234417,RMVar_hsa_circ_375351,RMVar_hsa_circ_374320,RMVar_hsa_circ_121056,RMVar_hsa_circ_96684,RMVar_hsa_circ_33747,RMVar_hsa_circ_234419,RMVar_hsa_circ_42618,RMVar_hsa_circ_51087,RMVar_hsa_circ_32623,RMVar_hsa_circ_234421,RMVar_hsa_circ_234420,RMVar_hsa_circ_90522,RMVar_hsa_circ_234418,RMVar_hsa_circ_65305,RMVar_hsa_circ_71595,RMVar_hsa_circ_234429,RMVar_hsa_circ_269349,RMVar_hsa_circ_126922,RMVar_hsa_circ_76295,RMVar_hsa_circ_123040,RMVar_hsa_circ_234430,RMVar_hsa_circ_234431,RMVar_hsa_circ_234433,RMVar_hsa_circ_106211,RMVar_hsa_circ_36844,RMVar_hsa_circ_234434,RMVar_hsa_circ_234435,RMVar_hsa_circ_337012 46965 RMVar_ID_46965 Human_SNP_ID_251925848 A-to-I Human chr5 + 133082666 133082666 133082666 TTTTGTATTTTTTGTAGAGACAGGATTTTGCCATATTGCTCAGGCTGGTCTCAGATTCCTGAGCT TTTTGTATTTTTTGTAGAGACAGGATTTTGCCGTATTGCTCAGGCTGGTCTCAGATTCCTGAGCT A G HSPA4 Ensembl:ENSG00000170606 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1470100509 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70160,RMVar_hsa_circ_234416,RMVar_hsa_circ_88039,RMVar_hsa_circ_124578,RMVar_hsa_circ_234417,RMVar_hsa_circ_375351,RMVar_hsa_circ_374320,RMVar_hsa_circ_121056,RMVar_hsa_circ_96684,RMVar_hsa_circ_33747,RMVar_hsa_circ_234419,RMVar_hsa_circ_42618,RMVar_hsa_circ_51087,RMVar_hsa_circ_32623,RMVar_hsa_circ_234421,RMVar_hsa_circ_234420,RMVar_hsa_circ_90522,RMVar_hsa_circ_234418,RMVar_hsa_circ_65305,RMVar_hsa_circ_71595,RMVar_hsa_circ_234429,RMVar_hsa_circ_269349,RMVar_hsa_circ_126922,RMVar_hsa_circ_76295,RMVar_hsa_circ_123040,RMVar_hsa_circ_234430,RMVar_hsa_circ_234431,RMVar_hsa_circ_234433,RMVar_hsa_circ_106211,RMVar_hsa_circ_36844,RMVar_hsa_circ_234434,RMVar_hsa_circ_234435,RMVar_hsa_circ_337012 46966 RMVar_ID_46966 Human_SNP_ID_251925929 A-to-I Human chr5 + 133082970 133082970 133082970 CCAGCTGGCCAATATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCCGGGTGTAGTGG CCAGCTGGCCAATATGGTGAAACCCCATCTCTGCTAAAAATACAAAAATTAGCCGGGTGTAGTGG A G HSPA4 Ensembl:ENSG00000170606 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs764231202 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70160,RMVar_hsa_circ_234416,RMVar_hsa_circ_88039,RMVar_hsa_circ_124578,RMVar_hsa_circ_234417,RMVar_hsa_circ_375351,RMVar_hsa_circ_374320,RMVar_hsa_circ_121056,RMVar_hsa_circ_96684,RMVar_hsa_circ_33747,RMVar_hsa_circ_234419,RMVar_hsa_circ_42618,RMVar_hsa_circ_51087,RMVar_hsa_circ_32623,RMVar_hsa_circ_234421,RMVar_hsa_circ_234420,RMVar_hsa_circ_90522,RMVar_hsa_circ_234418,RMVar_hsa_circ_65305,RMVar_hsa_circ_71595,RMVar_hsa_circ_234429,RMVar_hsa_circ_269349,RMVar_hsa_circ_126922,RMVar_hsa_circ_76295,RMVar_hsa_circ_123040,RMVar_hsa_circ_234430,RMVar_hsa_circ_234431,RMVar_hsa_circ_234433,RMVar_hsa_circ_106211,RMVar_hsa_circ_36844,RMVar_hsa_circ_234434,RMVar_hsa_circ_234435,RMVar_hsa_circ_337012 46967 RMVar_ID_46967 Human_SNP_ID_251926138 A-to-I Human chr5 + 133083663 133083663 133083663 GGGTTCAAGTGATTCTCCTGCCTCAGCTTCCCAAGTAGCTGGGGTTACAGGCATGCACCACCACA GGGTTCAAGTGATTCTCCTGCCTCAGCTTCCCGAGTAGCTGGGGTTACAGGCATGCACCACCACA A G HSPA4 Ensembl:ENSG00000170606 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1434965941 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70160,RMVar_hsa_circ_234416,RMVar_hsa_circ_88039,RMVar_hsa_circ_124578,RMVar_hsa_circ_234417,RMVar_hsa_circ_375351,RMVar_hsa_circ_374320,RMVar_hsa_circ_121056,RMVar_hsa_circ_96684,RMVar_hsa_circ_33747,RMVar_hsa_circ_234419,RMVar_hsa_circ_42618,RMVar_hsa_circ_51087,RMVar_hsa_circ_32623,RMVar_hsa_circ_234421,RMVar_hsa_circ_234420,RMVar_hsa_circ_90522,RMVar_hsa_circ_234418,RMVar_hsa_circ_65305,RMVar_hsa_circ_71595,RMVar_hsa_circ_234429,RMVar_hsa_circ_269349,RMVar_hsa_circ_126922,RMVar_hsa_circ_76295,RMVar_hsa_circ_123040,RMVar_hsa_circ_234430,RMVar_hsa_circ_234431,RMVar_hsa_circ_234433,RMVar_hsa_circ_106211,RMVar_hsa_circ_36844,RMVar_hsa_circ_234434,RMVar_hsa_circ_234435,RMVar_hsa_circ_337012 46968 RMVar_ID_46968 Human_SNP_ID_251928913 A-to-I Human chr5 + 133093608 133093608 133093608 CGCCTTCCAGGTTCAAGCGATTCTTATGCCTCAGCCTCCTGGGTAGCTGGGACTACAGGCGTGCA CGCCTTCCAGGTTCAAGCGATTCTTATGCCTCTGCCTCCTGGGTAGCTGGGACTACAGGCGTGCA A T HSPA4 Ensembl:ENSG00000170606 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1030724401 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14806,RMVar_hsa_circ_70160,RMVar_hsa_circ_124578,RMVar_hsa_circ_234417,RMVar_hsa_circ_121056,RMVar_hsa_circ_96684,RMVar_hsa_circ_234419,RMVar_hsa_circ_42618,RMVar_hsa_circ_90522,RMVar_hsa_circ_234418,RMVar_hsa_circ_71595,RMVar_hsa_circ_234429,RMVar_hsa_circ_123040,RMVar_hsa_circ_234431,RMVar_hsa_circ_234433,RMVar_hsa_circ_337012,RMVar_hsa_circ_363890,RMVar_hsa_circ_234439,RMVar_hsa_circ_30996,RMVar_hsa_circ_268513,RMVar_hsa_circ_341278,RMVar_hsa_circ_281171,RMVar_hsa_circ_234441,RMVar_hsa_circ_324463,RMVar_hsa_circ_357962,RMVar_hsa_circ_284219,RMVar_hsa_circ_234442 46969 RMVar_ID_46969 Human_SNP_ID_251928988 A-to-I Human chr5 + 133093946 133093946 133093946 GAAACCCCGTCTCTACTAAAAATACAAAATTTATCCCAGTGGGGTGGTACACGCTGGTAGCTCCA GAAACCCCGTCTCTACTAAAAATACAAAATTTGTCCCAGTGGGGTGGTACACGCTGGTAGCTCCA A G HSPA4 Ensembl:ENSG00000170606 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1441162883 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14806,RMVar_hsa_circ_70160,RMVar_hsa_circ_124578,RMVar_hsa_circ_234417,RMVar_hsa_circ_121056,RMVar_hsa_circ_96684,RMVar_hsa_circ_234419,RMVar_hsa_circ_42618,RMVar_hsa_circ_90522,RMVar_hsa_circ_234418,RMVar_hsa_circ_71595,RMVar_hsa_circ_234429,RMVar_hsa_circ_123040,RMVar_hsa_circ_234431,RMVar_hsa_circ_234433,RMVar_hsa_circ_337012,RMVar_hsa_circ_363890,RMVar_hsa_circ_234439,RMVar_hsa_circ_30996,RMVar_hsa_circ_268513,RMVar_hsa_circ_341278,RMVar_hsa_circ_281171,RMVar_hsa_circ_234441,RMVar_hsa_circ_324463,RMVar_hsa_circ_357962,RMVar_hsa_circ_284219,RMVar_hsa_circ_234442 46970 RMVar_ID_46970 Human_SNP_ID_252133862 A-to-I Human chr5 - 133961720 133961720 133961720 ATATATGAAAAATAAAAAAAGCCAGGCAGGGTAGCATGTGCCTGTGGTCCCAGCTACATGGGGGG ATATATGAAAAATAAAAAAAGCCAGGCAGGGTGGCATGTGCCTGTGGTCCCAGCTACATGGGGGG T C C5orf15 Ensembl:ENSG00000113583 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs959191970 Functional Loss SNV dbSNP153 33..33 33 - - - 46971 RMVar_ID_46971 Human_SNP_ID_252136847 A-to-I Human chr5 - 133974736 133974736 133974736 GTTGGTCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCTGCCTGCCTCGGCCTCCCAAAATGC GTTGGTCAGGCTGGTCTCGAACTCCTGACCTCTGGTGATCTGCCTGCCTCGGCCTCCCAAAATGC T A VDAC1 Ensembl:ENSG00000213585 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1348866350 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110571,RMVar_hsa_circ_234449,RMVar_hsa_circ_370165,RMVar_hsa_circ_234448,RMVar_hsa_circ_371521,RMVar_hsa_circ_234450 46972 RMVar_ID_46972 Human_SNP_ID_252136848 A-to-I Human chr5 - 133974736 133974736 133974736 GTTGGTCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCTGCCTGCCTCGGCCTCCCAAAATGC GTTGGTCAGGCTGGTCTCGAACTCCTGACCTCCGGTGATCTGCCTGCCTCGGCCTCCCAAAATGC T G VDAC1 Ensembl:ENSG00000213585 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1348866350 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110571,RMVar_hsa_circ_234449,RMVar_hsa_circ_370165,RMVar_hsa_circ_234448,RMVar_hsa_circ_371521,RMVar_hsa_circ_234450 46973 RMVar_ID_46973 Human_SNP_ID_252136968 A-to-I Human chr5 - 133975211 133975211 133975211 CCAGGTTGGATGCAGTGGTGTAATTGCAGCTCACTGCAGCCTCATCCTCCTGTGCTCAAGTAATC CCAGGTTGGATGCAGTGGTGTAATTGCAGCTCGCTGCAGCCTCATCCTCCTGTGCTCAAGTAATC T C VDAC1 Ensembl:ENSG00000213585 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1233690637 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15298365 RMVar_hsa_circ_110571,RMVar_hsa_circ_234449,RMVar_hsa_circ_370165,RMVar_hsa_circ_234448,RMVar_hsa_circ_371521,RMVar_hsa_circ_234450 46974 RMVar_ID_46974 Human_SNP_ID_252137418 A-to-I Human chr5 - 133976992 133976992 133976992 TCACCCAGACTGGAGTGCAGTGGTGAGATCTCAGCTCACTGCAACCTCTGCCTCCTGGGTTCAGA TCACCCAGACTGGAGTGCAGTGGTGAGATCTCGGCTCACTGCAACCTCTGCCTCCTGGGTTCAGA T C VDAC1 Ensembl:ENSG00000213585 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1007594124 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56787,RMVar_hsa_circ_110571,RMVar_hsa_circ_234449,RMVar_hsa_circ_370165,RMVar_hsa_circ_234448,RMVar_hsa_circ_371521,RMVar_hsa_circ_234450,RMVar_hsa_circ_374292,RMVar_hsa_circ_234452 46975 RMVar_ID_46975 Human_SNP_ID_252137953 A-to-I Human chr5 - 133979601 133979601 133979601 AGAAGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCTGGGCGTGGTGGCGGGTGCCTGT AGAAGGTGAAACCCCATCTCTACTAAAAATACGAAAATTAGCTGGGCGTGGTGGCGGGTGCCTGT T C VDAC1 Ensembl:ENSG00000213585 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1220856668 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56787,RMVar_hsa_circ_110571,RMVar_hsa_circ_234449,RMVar_hsa_circ_370165,RMVar_hsa_circ_234448,RMVar_hsa_circ_371521,RMVar_hsa_circ_234450,RMVar_hsa_circ_374292,RMVar_hsa_circ_234452 46976 RMVar_ID_46976 Human_SNP_ID_252139114 A-to-I Human chr5 - 133984158 133984158 133984158 CTAGCTACCTGGGAGGCTGAGGTGGGAGGATCACCTGAGCTCAGGAGGTAGGGGCTGTAGTGAGC CTAGCTACCTGGGAGGCTGAGGTGGGAGGATCTCCTGAGCTCAGGAGGTAGGGGCTGTAGTGAGC T A VDAC1 Ensembl:ENSG00000213585 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1479476337 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15298567 RMVar_hsa_circ_110571,RMVar_hsa_circ_234448,RMVar_hsa_circ_371521,RMVar_hsa_circ_234450,RMVar_hsa_circ_374292,RMVar_hsa_circ_234454,RMVar_hsa_circ_97455,RMVar_hsa_circ_234452,RMVar_hsa_circ_325223,RMVar_hsa_circ_107736,RMVar_hsa_circ_234455 46977 RMVar_ID_46977 Human_SNP_ID_252139491 A-to-I Human chr5 - 133985554 133985554 133985554 CACCTCCCAGGTTCAAGCAATTCTCGTGCCTCAGCCTCCTGAATAGCTGGGATTACAGGCACATG CACCTCCCAGGTTCAAGCAATTCTCGTGCCTCGGCCTCCTGAATAGCTGGGATTACAGGCACATG T C VDAC1 Ensembl:ENSG00000213585 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs367670101 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25854763 RMVar_hsa_circ_110571,RMVar_hsa_circ_234448,RMVar_hsa_circ_371521,RMVar_hsa_circ_234450,RMVar_hsa_circ_374292,RMVar_hsa_circ_234454,RMVar_hsa_circ_97455,RMVar_hsa_circ_234452,RMVar_hsa_circ_325223,RMVar_hsa_circ_107736,RMVar_hsa_circ_234455 46978 RMVar_ID_46978 Human_SNP_ID_252140129 A-to-I Human chr5 - 133988430 133988430 133988430 AGGAATGCACCACCACACCCAGCTAATTTTGTATTTTTAATAGAGACAGGGTCTCTCCATGTTGG AGGAATGCACCACCACACCCAGCTAATTTTGTGTTTTTAATAGAGACAGGGTCTCTCCATGTTGG T C VDAC1 Ensembl:ENSG00000213585 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs547036811 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15298719 RMVar_hsa_circ_110571,RMVar_hsa_circ_234448,RMVar_hsa_circ_371521,RMVar_hsa_circ_234450,RMVar_hsa_circ_374292,RMVar_hsa_circ_234454,RMVar_hsa_circ_97455,RMVar_hsa_circ_234452,RMVar_hsa_circ_325223,RMVar_hsa_circ_107736,RMVar_hsa_circ_234455 46979 RMVar_ID_46979 Human_SNP_ID_252167829 A-to-I Human chr5 - 134101382 134101382 134101382 TTTCACCATGTTGGCCGGGCTGGTCTCGAACTACTGACCTCGGGTGATCTGCCTGCCTCGGCCTC TTTCACCATGTTGGCCGGGCTGGTCTCGAACTGCTGACCTCGGGTGATCTGCCTGCCTCGGCCTC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1412294536 Functional Loss SNV dbSNP153 33..33 33 - - - 46980 RMVar_ID_46980 Human_SNP_ID_252181769 A-to-I Human chr5 - 134153419 134153419 134153419 TGGAGTGCAGTGATGTGATCACAGCTCATTGCAGCCTCGAACTCTTGGGCTCCAACAGTCCTCCT TGGAGTGCAGTGATGTGATCACAGCTCATTGCGGCCTCGAACTCTTGGGCTCCAACAGTCCTCCT T C SKP1 Ensembl:ENSG00000113558 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1458382952 Functional Loss SNV dbSNP153 33..33 33 - - - 46981 RMVar_ID_46981 Human_SNP_ID_252183329 A-to-I Human chr5 - 134159491 134159491 134159491 CTGTAATCCCAGCTACTTGGGAGACTGAAGCAAGAGAATTGGCTGAACCTAGGAGGTAGAGATTG CTGTAATCCCAGCTACTTGGGAGACTGAAGCAGGAGAATTGGCTGAACCTAGGAGGTAGAGATTG T C SKP1 Ensembl:ENSG00000113558 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1469196292 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_378921,RMVar_hsa_circ_55852,RMVar_hsa_circ_234462,RMVar_hsa_circ_80457,RMVar_hsa_circ_234465,RMVar_hsa_circ_378031,RMVar_hsa_circ_234461,RMVar_hsa_circ_377328,RMVar_hsa_circ_234464,RMVar_hsa_circ_300155,RMVar_hsa_circ_234466,RMVar_hsa_circ_25318 46982 RMVar_ID_46982 Human_SNP_ID_252195656 A-to-I Human chr5 - 134207322 134207322 134207322 TGGCTCACGGCAACCTCCACCTCCCAAGTTTAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGCT TGGCTCACGGCAACCTCCACCTCCCAAGTTTAGGCAATTCTCCTGCCTCAGCCTCCCAAGTAGCT T C PPP2CA,AC104109.4,AC104109.3 Ensembl:ENSG00000113575,Ensembl:ENSG00000273345,Ensembl:ENSG00000272772 Protein coding,lincRNA,Protein coding intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1189078549 Functional Loss SNV dbSNP153 33..33 33 - - - 46983 RMVar_ID_46983 Human_SNP_ID_252195753 A-to-I Human chr5 - 134207709 134207709 134207709 CCTCACCTCTACAAAAAGTGCAAAATAGGCATAGTGGTGCACACCTGTGGTCGCAATTGTTCATG CCTCACCTCTACAAAAAGTGCAAAATAGGCATGGTGGTGCACACCTGTGGTCGCAATTGTTCATG T C PPP2CA,AC104109.4,AC104109.3 Ensembl:ENSG00000113575,Ensembl:ENSG00000273345,Ensembl:ENSG00000272772 Protein coding,lincRNA,Protein coding intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs189737525 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7384281 46984 RMVar_ID_46984 Human_SNP_ID_252196629 A-to-I Human chr5 - 134211207 134211207 134211207 GCATGCCTGCAGTCCCAGCTACTCGGGAGACTAAGGTGGGAGGATTACTTGAGCTTGGGAGATCA GCATGCCTGCAGTCCCAGCTACTCGGGAGACTGAGGTGGGAGGATTACTTGAGCTTGGGAGATCA T C PPP2CA,AC104109.4,AC104109.3 Ensembl:ENSG00000113575,Ensembl:ENSG00000273345,Ensembl:ENSG00000272772 Protein coding,lincRNA,Protein coding intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1372782865 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25855188 46985 RMVar_ID_46985 Human_SNP_ID_252196814 A-to-I Human chr5 - 134211900 134211900 134211900 TTGGCCAGGCTGGTTTCGAACTCCCGACCTCAAGTGATTCATCCGCCTTGGCATCCCATAGTGCT TTGGCCAGGCTGGTTTCGAACTCCCGACCTCAGGTGATTCATCCGCCTTGGCATCCCATAGTGCT T C PPP2CA,AC104109.4,AC104109.3 Ensembl:ENSG00000113575,Ensembl:ENSG00000273345,Ensembl:ENSG00000272772 Protein coding,lincRNA,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs933527725 Functional Loss SNV dbSNP153 33..33 33 - - - 46986 RMVar_ID_46986 Human_SNP_ID_252199042 A-to-I Human chr5 - 134220208 134220208 134220208 GTGATCCACCCATCTCAGCCTCCCAAAGTGCTAGGATTACAGGCATGAGCCACTGGCACCAGACC GTGATCCACCCATCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGGCACCAGACC T C PPP2CA,AC104109.4,AC104109.3 Ensembl:ENSG00000113575,Ensembl:ENSG00000273345,Ensembl:ENSG00000272772 Protein coding,lincRNA,Protein coding intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs536744236 Functional Loss SNV dbSNP153 33..33 33 - - - 46987 RMVar_ID_46987 Human_SNP_ID_252199688 A-to-I Human chr5 - 134222363 134222363 134222363 GCTGAAAAATATTTGACCAAGATGACATTCTTATATGAATTGGGTAATATGTTGCTGTGAGTATG GCTGAAAAATATTTGACCAAGATGACATTCTTTTATGAATTGGGTAATATGTTGCTGTGAGTATG T A PPP2CA,AC104109.4,AC104109.3 Ensembl:ENSG00000113575,Ensembl:ENSG00000273345,Ensembl:ENSG00000272772 Protein coding,lincRNA,Protein coding intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs254050 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24083216 GWAS_ID_5737,GWAS_ID_5738,GWAS_ID_5739,GWAS_ID_5740,GWAS_ID_5741,GWAS_ID_5742 46988 RMVar_ID_46988 Human_SNP_ID_252199689 A-to-I Human chr5 - 134222363 134222363 134222363 GCTGAAAAATATTTGACCAAGATGACATTCTTATATGAATTGGGTAATATGTTGCTGTGAGTATG GCTGAAAAATATTTGACCAAGATGACATTCTTGTATGAATTGGGTAATATGTTGCTGTGAGTATG T C PPP2CA,AC104109.4,AC104109.3 Ensembl:ENSG00000113575,Ensembl:ENSG00000273345,Ensembl:ENSG00000272772 Protein coding,lincRNA,Protein coding intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs254050 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24083216 GWAS_ID_5737,GWAS_ID_5738,GWAS_ID_5739,GWAS_ID_5740,GWAS_ID_5741,GWAS_ID_5742 46989 RMVar_ID_46989 Human_SNP_ID_252200124 A-to-I Human chr5 - 134224066 134224066 134224066 TCTTTTGAAGAAAACGTGGAAAGGAGGGAGGTAATGACGTAACTGGAAGACTGGACTGCGAGTTA TCTTTTGAAGAAAACGTGGAAAGGAGGGAGGTGATGACGTAACTGGAAGACTGGACTGCGAGTTA T C PPP2CA,AC104109.4,AC104109.3 Ensembl:ENSG00000113575,Ensembl:ENSG00000273345,Ensembl:ENSG00000272772 Protein coding,lincRNA,Protein coding intron,intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2284317 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1108222,Human_RBP_ID_25855277 GWAS_ID_5743,GWAS_ID_5744,GWAS_ID_5745,GWAS_ID_5746,GWAS_ID_5747,GWAS_ID_5748,GWAS_ID_5749,GWAS_ID_5750,GWAS_ID_5751,GWAS_ID_5752,GWAS_ID_5753,GWAS_ID_5754,GWAS_ID_5755,GWAS_ID_5756,GWAS_ID_5757,GWAS_ID_5758,GWAS_ID_5759,GWAS_ID_5760,GWAS_ID_5761,GWAS_ID_5762,GWAS_ID_5763,GWAS_ID_5764,GWAS_ID_5765,GWAS_ID_5766,GWAS_ID_5767,GWAS_ID_5768,GWAS_ID_5769,GWAS_ID_5770,GWAS_ID_5771,GWAS_ID_5772,GWAS_ID_5773,GWAS_ID_5774,GWAS_ID_5775,GWAS_ID_5776,GWAS_ID_5777,GWAS_ID_5778,GWAS_ID_5779 46990 RMVar_ID_46990 Human_SNP_ID_252221407 A-to-I Human chr5 - 134316054 134316054 134316054 CCTGCTACTTTGGAGGCTGAGGTGGCAGGATCACTTGAGCCTGGGAGGTTGAGGCTGCAGTGAGT CCTGCTACTTTGGAGGCTGAGGTGGCAGGATCGCTTGAGCCTGGGAGGTTGAGGCTGCAGTGAGT T C CDKL3,AC104109.4 Ensembl:ENSG00000006837,Ensembl:ENSG00000273345 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1254611084 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_300218,RMVar_hsa_circ_36778,RMVar_hsa_circ_234480,RMVar_hsa_circ_234481,RMVar_hsa_circ_314997,RMVar_hsa_circ_328096,RMVar_hsa_circ_329786,RMVar_hsa_circ_234485,RMVar_hsa_circ_234486,RMVar_hsa_circ_234487,RMVar_hsa_circ_234484,RMVar_hsa_circ_234488,RMVar_hsa_circ_30151,RMVar_hsa_circ_342434,RMVar_hsa_circ_234489,RMVar_hsa_circ_234490,RMVar_hsa_circ_321964,RMVar_hsa_circ_299024,RMVar_hsa_circ_341369,RMVar_hsa_circ_234492,RMVar_hsa_circ_234496,RMVar_hsa_circ_288491,RMVar_hsa_circ_344187,RMVar_hsa_circ_234491,RMVar_hsa_circ_297291,RMVar_hsa_circ_270207,RMVar_hsa_circ_234494,RMVar_hsa_circ_234495,RMVar_hsa_circ_234493 46991 RMVar_ID_46991 Human_SNP_ID_252221413 A-to-I Human chr5 - 134316093 134316093 134316093 AAAAAACTAGCCAGGCACAGTGGCATGCGCCTATAGTCCCCTGCTACTTTGGAGGCTGAGGTGGC AAAAAACTAGCCAGGCACAGTGGCATGCGCCTGTAGTCCCCTGCTACTTTGGAGGCTGAGGTGGC T C CDKL3,AC104109.4 Ensembl:ENSG00000006837,Ensembl:ENSG00000273345 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs933455309 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_300218,RMVar_hsa_circ_36778,RMVar_hsa_circ_234480,RMVar_hsa_circ_234481,RMVar_hsa_circ_314997,RMVar_hsa_circ_328096,RMVar_hsa_circ_329786,RMVar_hsa_circ_234485,RMVar_hsa_circ_234486,RMVar_hsa_circ_234487,RMVar_hsa_circ_234484,RMVar_hsa_circ_234488,RMVar_hsa_circ_30151,RMVar_hsa_circ_342434,RMVar_hsa_circ_234489,RMVar_hsa_circ_234490,RMVar_hsa_circ_321964,RMVar_hsa_circ_299024,RMVar_hsa_circ_341369,RMVar_hsa_circ_234492,RMVar_hsa_circ_234496,RMVar_hsa_circ_288491,RMVar_hsa_circ_344187,RMVar_hsa_circ_234491,RMVar_hsa_circ_297291,RMVar_hsa_circ_270207,RMVar_hsa_circ_234494,RMVar_hsa_circ_234495,RMVar_hsa_circ_234493 46992 RMVar_ID_46992 Human_SNP_ID_252221879 A-to-I Human chr5 - 134318132 134318132 134318132 TCACCACAACCTCCGCCTCCTGGGTTGAAGCAATTTTCCTGCCTCAGCCTCCCAAGTAGCTGGGA TCACCACAACCTCCGCCTCCTGGGTTGAAGCAGTTTTCCTGCCTCAGCCTCCCAAGTAGCTGGGA T C CDKL3,AC104109.4 Ensembl:ENSG00000006837,Ensembl:ENSG00000273345 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1356969199 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_300218,RMVar_hsa_circ_36778,RMVar_hsa_circ_234480,RMVar_hsa_circ_234481,RMVar_hsa_circ_314997,RMVar_hsa_circ_328096,RMVar_hsa_circ_329786,RMVar_hsa_circ_234485,RMVar_hsa_circ_234486,RMVar_hsa_circ_234487,RMVar_hsa_circ_234484,RMVar_hsa_circ_234488,RMVar_hsa_circ_30151,RMVar_hsa_circ_342434,RMVar_hsa_circ_234489,RMVar_hsa_circ_234490,RMVar_hsa_circ_321964,RMVar_hsa_circ_299024,RMVar_hsa_circ_341369,RMVar_hsa_circ_234492,RMVar_hsa_circ_234496,RMVar_hsa_circ_288491,RMVar_hsa_circ_344187,RMVar_hsa_circ_234491,RMVar_hsa_circ_297291,RMVar_hsa_circ_270207,RMVar_hsa_circ_234494,RMVar_hsa_circ_234495,RMVar_hsa_circ_234493 46993 RMVar_ID_46993 Human_SNP_ID_252221999 A-to-I Human chr5 - 134318666 134318666 134318666 CCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAAGTTAGCTGGGCATGGTGGCA CCTGGCCAACATGGTGAAACCCCGTCTCTACTGAAAATACAAAAAGTTAGCTGGGCATGGTGGCA T C CDKL3,AC104109.4 Ensembl:ENSG00000006837,Ensembl:ENSG00000273345 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1002267280 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_300218,RMVar_hsa_circ_36778,RMVar_hsa_circ_234480,RMVar_hsa_circ_234481,RMVar_hsa_circ_314997,RMVar_hsa_circ_328096,RMVar_hsa_circ_329786,RMVar_hsa_circ_234485,RMVar_hsa_circ_234486,RMVar_hsa_circ_234487,RMVar_hsa_circ_234484,RMVar_hsa_circ_234488,RMVar_hsa_circ_30151,RMVar_hsa_circ_342434,RMVar_hsa_circ_234489,RMVar_hsa_circ_234490,RMVar_hsa_circ_321964,RMVar_hsa_circ_299024,RMVar_hsa_circ_341369,RMVar_hsa_circ_234492,RMVar_hsa_circ_234496,RMVar_hsa_circ_288491,RMVar_hsa_circ_344187,RMVar_hsa_circ_234491,RMVar_hsa_circ_297291,RMVar_hsa_circ_270207,RMVar_hsa_circ_234494,RMVar_hsa_circ_234495,RMVar_hsa_circ_234493 46994 RMVar_ID_46994 Human_SNP_ID_252222013 A-to-I Human chr5 - 134318714 134318714 134318714 TTGGGACGCCGAGACGGGCTGATCACGAGGTCAGGAGATCAAGACCATCCTGGCCAACATGGTGA TTGGGACGCCGAGACGGGCTGATCACGAGGTCGGGAGATCAAGACCATCCTGGCCAACATGGTGA T C CDKL3,AC104109.4 Ensembl:ENSG00000006837,Ensembl:ENSG00000273345 Protein coding,lincRNA intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs965609984 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_300218,RMVar_hsa_circ_36778,RMVar_hsa_circ_234480,RMVar_hsa_circ_234481,RMVar_hsa_circ_314997,RMVar_hsa_circ_328096,RMVar_hsa_circ_329786,RMVar_hsa_circ_234485,RMVar_hsa_circ_234486,RMVar_hsa_circ_234487,RMVar_hsa_circ_234484,RMVar_hsa_circ_234488,RMVar_hsa_circ_30151,RMVar_hsa_circ_342434,RMVar_hsa_circ_234489,RMVar_hsa_circ_234490,RMVar_hsa_circ_321964,RMVar_hsa_circ_299024,RMVar_hsa_circ_341369,RMVar_hsa_circ_234492,RMVar_hsa_circ_234496,RMVar_hsa_circ_288491,RMVar_hsa_circ_344187,RMVar_hsa_circ_234491,RMVar_hsa_circ_297291,RMVar_hsa_circ_270207,RMVar_hsa_circ_234494,RMVar_hsa_circ_234495,RMVar_hsa_circ_234493 46995 RMVar_ID_46995 Human_SNP_ID_252222028 A-to-I Human chr5 - 134318758 134318758 134318758 GAAATGGGCCAGGCAGGGTGGCTTATGTGTGTAATCCCAGCACTTTGGGACGCCGAGACGGGCTG GAAATGGGCCAGGCAGGGTGGCTTATGTGTGTTATCCCAGCACTTTGGGACGCCGAGACGGGCTG T A CDKL3,AC104109.4 Ensembl:ENSG00000006837,Ensembl:ENSG00000273345 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1381179054 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_300218,RMVar_hsa_circ_36778,RMVar_hsa_circ_234480,RMVar_hsa_circ_234481,RMVar_hsa_circ_314997,RMVar_hsa_circ_328096,RMVar_hsa_circ_329786,RMVar_hsa_circ_234485,RMVar_hsa_circ_234486,RMVar_hsa_circ_234487,RMVar_hsa_circ_234484,RMVar_hsa_circ_234488,RMVar_hsa_circ_30151,RMVar_hsa_circ_342434,RMVar_hsa_circ_234489,RMVar_hsa_circ_234490,RMVar_hsa_circ_321964,RMVar_hsa_circ_299024,RMVar_hsa_circ_341369,RMVar_hsa_circ_234492,RMVar_hsa_circ_234496,RMVar_hsa_circ_288491,RMVar_hsa_circ_344187,RMVar_hsa_circ_234491,RMVar_hsa_circ_297291,RMVar_hsa_circ_270207,RMVar_hsa_circ_234494,RMVar_hsa_circ_234495,RMVar_hsa_circ_234493 46996 RMVar_ID_46996 Human_SNP_ID_252222142 A-to-I Human chr5 - 134319207 134319207 134319207 CCTGCCTCAGCCTTCCGAGTAGTTGGGATTACAGGCACCTGCCACCATGCCCGGCTAATTTTTGT CCTGCCTCAGCCTTCCGAGTAGTTGGGATTACGGGCACCTGCCACCATGCCCGGCTAATTTTTGT T C CDKL3,AC104109.4 Ensembl:ENSG00000006837,Ensembl:ENSG00000273345 Protein coding,lincRNA intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs981937191 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_300218,RMVar_hsa_circ_36778,RMVar_hsa_circ_234480,RMVar_hsa_circ_234481,RMVar_hsa_circ_314997,RMVar_hsa_circ_328096,RMVar_hsa_circ_329786,RMVar_hsa_circ_234485,RMVar_hsa_circ_234486,RMVar_hsa_circ_234487,RMVar_hsa_circ_234484,RMVar_hsa_circ_234488,RMVar_hsa_circ_30151,RMVar_hsa_circ_342434,RMVar_hsa_circ_234489,RMVar_hsa_circ_234490,RMVar_hsa_circ_321964,RMVar_hsa_circ_299024,RMVar_hsa_circ_341369,RMVar_hsa_circ_234492,RMVar_hsa_circ_234496,RMVar_hsa_circ_288491,RMVar_hsa_circ_344187,RMVar_hsa_circ_234491,RMVar_hsa_circ_297291,RMVar_hsa_circ_270207,RMVar_hsa_circ_234494,RMVar_hsa_circ_234495,RMVar_hsa_circ_234493 46997 RMVar_ID_46997 Human_SNP_ID_252222168 A-to-I Human chr5 - 134319324 134319324 134319324 TATGTTTTTTTTTTTTTTCCTCCCCCGGAGACAGAGTCTTGCTCTGTCGCCCAGGCTGTAGTGCA TATGTTTTTTTTTTTTTTCCTCCCCCGGAGACGGAGTCTTGCTCTGTCGCCCAGGCTGTAGTGCA T C CDKL3,AC104109.4 Ensembl:ENSG00000006837,Ensembl:ENSG00000273345 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1433722213 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_300218,RMVar_hsa_circ_36778,RMVar_hsa_circ_234480,RMVar_hsa_circ_234481,RMVar_hsa_circ_314997,RMVar_hsa_circ_328096,RMVar_hsa_circ_329786,RMVar_hsa_circ_234485,RMVar_hsa_circ_234486,RMVar_hsa_circ_234487,RMVar_hsa_circ_234484,RMVar_hsa_circ_234488,RMVar_hsa_circ_30151,RMVar_hsa_circ_342434,RMVar_hsa_circ_234489,RMVar_hsa_circ_234490,RMVar_hsa_circ_321964,RMVar_hsa_circ_299024,RMVar_hsa_circ_341369,RMVar_hsa_circ_234492,RMVar_hsa_circ_234496,RMVar_hsa_circ_288491,RMVar_hsa_circ_344187,RMVar_hsa_circ_234491,RMVar_hsa_circ_297291,RMVar_hsa_circ_270207,RMVar_hsa_circ_234494,RMVar_hsa_circ_234495,RMVar_hsa_circ_234493 46998 RMVar_ID_46998 Human_SNP_ID_252234407 A-to-I Human chr5 - 134370122 134370122 134370122 AGCCTTGCCCCTGATTCCATGGAAGCAGAGTTAACTTTTCTGACTTTCCTTGTACCTCTTTCTTC AGCCTTGCCCCTGATTCCATGGAAGCAGAGTTCACTTTTCTGACTTTCCTTGTACCTCTTTCTTC T G CDKL3,AC104109.4 Ensembl:ENSG00000006837,Ensembl:ENSG00000273345 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256865526 Functional Loss SNV dbSNP153 33..33 33 - - - 46999 RMVar_ID_46999 Human_SNP_ID_252236770 A-to-I Human chr5 + 134378062 134378062 134378062 AAAATTAGCCAGGCATGGTGGTACATGCCTTTAGTCCCAGCTACTTGGGAGGATTACCTGAGCCC AAAATTAGCCAGGCATGGTGGTACATGCCTTTTGTCCCAGCTACTTGGGAGGATTACCTGAGCCC A T UBE2B Ensembl:ENSG00000119048 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs113978617 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34838,RMVar_hsa_circ_354403 47000 RMVar_ID_47000 Human_SNP_ID_252237676 A-to-I Human chr5 + 134381500 134381500 134381500 TGTGTGTTGCCCAGGCTGGTCCTTGAACTCCTAGCCTCAAGCAGTCCTCCCACTTTGACCTCCCA TGTGTGTTGCCCAGGCTGGTCCTTGAACTCCTGGCCTCAAGCAGTCCTCCCACTTTGACCTCCCA A G UBE2B Ensembl:ENSG00000119048 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1183626583 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7384681,Human_RBP_ID_15301423,Human_RBP_ID_17575308 RMVar_hsa_circ_34838,RMVar_hsa_circ_234504,RMVar_hsa_circ_234505,RMVar_hsa_circ_354403 47001 RMVar_ID_47001 Human_SNP_ID_252237718 A-to-I Human chr5 + 134381686 134381686 134381686 TAATACATGGTCGGGCATGGTGGCTCATACCTATAAACTCAGCACTTTGGGAGGCCAAGGTGGGC TAATACATGGTCGGGCATGGTGGCTCATACCTGTAAACTCAGCACTTTGGGAGGCCAAGGTGGGC A G UBE2B Ensembl:ENSG00000119048 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1161872005 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25936558 RMVar_hsa_circ_34838,RMVar_hsa_circ_234504,RMVar_hsa_circ_234505,RMVar_hsa_circ_354403 47002 RMVar_ID_47002 Human_SNP_ID_252237772 A-to-I Human chr5 + 134381899 134381899 134381899 CTGGGAGACGGAGGTTGCAGTGAGCTGAGCTCACAACACTGCACTTCAGCCTGGGTGACAAACCA CTGGGAGACGGAGGTTGCAGTGAGCTGAGCTCGCAACACTGCACTTCAGCCTGGGTGACAAACCA A G UBE2B Ensembl:ENSG00000119048 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1454156849 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8602696,Human_RBP_ID_15301434,Human_RBP_ID_25936559 RMVar_hsa_circ_34838,RMVar_hsa_circ_234504,RMVar_hsa_circ_234505,RMVar_hsa_circ_354403 47003 RMVar_ID_47003 Human_SNP_ID_252237831 A-to-I Human chr5 + 134382250 134382249 134382251 CAAGGTGGGAAGGTTGCTTGAGACCAGGAGTCAGAGACCAGCCTGGGCAACATAGCGAGGTCCCA CAAGGTGGGAAGGTTGCTTGAGACCAGGAGTC__AGACCAGCCTGGGCAACATAGCGAGGTCCCA CAG C UBE2B Ensembl:ENSG00000119048 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1304665804 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_34838,RMVar_hsa_circ_234504,RMVar_hsa_circ_234505,RMVar_hsa_circ_354403 47004 RMVar_ID_47004 Human_SNP_ID_252237833 A-to-I Human chr5 + 134382250 134382250 134382250 CAAGGTGGGAAGGTTGCTTGAGACCAGGAGTCAGAGACCAGCCTGGGCAACATAGCGAGGTCCCA CAAGGTGGGAAGGTTGCTTGAGACCAGGAGTCGGAGACCAGCCTGGGCAACATAGCGAGGTCCCA A G UBE2B Ensembl:ENSG00000119048 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs932321996 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34838,RMVar_hsa_circ_234504,RMVar_hsa_circ_234505,RMVar_hsa_circ_354403 47005 RMVar_ID_47005 Human_SNP_ID_252238024 A-to-I Human chr5 + 134383054 134383054 134383054 GGGCATGGTGGCGCATGCCTGTGGTCCCAGCTACTCGGGAGGCTGAGGCGGGAGAATTGCTTGAA GGGCATGGTGGCGCATGCCTGTGGTCCCAGCTGCTCGGGAGGCTGAGGCGGGAGAATTGCTTGAA A G UBE2B Ensembl:ENSG00000119048 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1312208005 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_166951 RMVar_hsa_circ_34838,RMVar_hsa_circ_234504,RMVar_hsa_circ_234505,RMVar_hsa_circ_354403 47006 RMVar_ID_47006 Human_SNP_ID_252238210 A-to-I Human chr5 + 134383600 134383600 134383600 TGCCTGTTGGGTTCAAGTGATTCTCTTGCCTCAGCCTCCCAAAGCTGTATATCCAGCTAATTTTT TGCCTGTTGGGTTCAAGTGATTCTCTTGCCTCTGCCTCCCAAAGCTGTATATCCAGCTAATTTTT A T UBE2B Ensembl:ENSG00000119048 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1415923085 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34838,RMVar_hsa_circ_234504,RMVar_hsa_circ_234505,RMVar_hsa_circ_354403 47007 RMVar_ID_47007 Human_SNP_ID_252239068 A-to-I Human chr5 + 134387125 134387125 134387125 GGGACTACACGCATGCACTACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCA GGGACTACACGCATGCACTACCATGCCTGGCTCATTTTTGTATTTTTAGTAGAGACAGGGTTTCA A C UBE2B Ensembl:ENSG00000119048 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1342897849 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34838,RMVar_hsa_circ_234504,RMVar_hsa_circ_234505,RMVar_hsa_circ_354403 47008 RMVar_ID_47008 Human_SNP_ID_252239251 A-to-I Human chr5 + 134388065 134388065 134388065 CCTCAAGCAATCCTGCCTGCCTCGGCCTCCCAAAGTGTTCAGGACTGGCGTGAGCCACCGTGCCC CCTCAAGCAATCCTGCCTGCCTCGGCCTCCCACAGTGTTCAGGACTGGCGTGAGCCACCGTGCCC A C UBE2B Ensembl:ENSG00000119048 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs550055301 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34838,RMVar_hsa_circ_234504,RMVar_hsa_circ_234505,RMVar_hsa_circ_354403 47009 RMVar_ID_47009 Human_SNP_ID_252239252 A-to-I Human chr5 + 134388065 134388065 134388065 CCTCAAGCAATCCTGCCTGCCTCGGCCTCCCAAAGTGTTCAGGACTGGCGTGAGCCACCGTGCCC CCTCAAGCAATCCTGCCTGCCTCGGCCTCCCAGAGTGTTCAGGACTGGCGTGAGCCACCGTGCCC A G UBE2B Ensembl:ENSG00000119048 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs550055301 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34838,RMVar_hsa_circ_234504,RMVar_hsa_circ_234505,RMVar_hsa_circ_354403 47010 RMVar_ID_47010 Human_SNP_ID_252240092 A-to-I Human chr5 + 134391845 134391845 134391845 AAAATTAGTTGGGCATAGTGGCACTTGCCTGTAGTCTCAGCTACTTAGGAGGCTGAGGTGGCAGA AAAATTAGTTGGGCATAGTGGCACTTGCCTGTCGTCTCAGCTACTTAGGAGGCTGAGGTGGCAGA A C UBE2B Ensembl:ENSG00000119048 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1308128491 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_234504 47011 RMVar_ID_47011 Human_SNP_ID_252240101 A-to-I Human chr5 + 134391891 134391891 134391891 AGGAGGCTGAGGTGGCAGAATAGCTTATGCCTAGGAGGTTGAGGCTGCAGTGAGCTGTGATTATG AGGAGGCTGAGGTGGCAGAATAGCTTATGCCTGGGAGGTTGAGGCTGCAGTGAGCTGTGATTATG A G UBE2B Ensembl:ENSG00000119048 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1423868740 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_631570 RMVar_hsa_circ_234504 47012 RMVar_ID_47012 Human_SNP_ID_252241072 A-to-I Human chr5 + 134396485 134396485 134396485 CAGTCTGGAATGCAGTCACATGATCACAGCTCACTACAGCCTGGAACCCTTGGACTCAAGCAGTT CAGTCTGGAATGCAGTCACATGATCACAGCTCCCTACAGCCTGGAACCCTTGGACTCAAGCAGTT A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886486189 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2895185 47013 RMVar_ID_47013 Human_SNP_ID_252241073 A-to-I Human chr5 + 134396485 134396485 134396485 CAGTCTGGAATGCAGTCACATGATCACAGCTCACTACAGCCTGGAACCCTTGGACTCAAGCAGTT CAGTCTGGAATGCAGTCACATGATCACAGCTCGCTACAGCCTGGAACCCTTGGACTCAAGCAGTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886486189 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2895185 47014 RMVar_ID_47014 Human_SNP_ID_252241887 A-to-I Human chr5 - 134399992 134399992 134399992 CTCTGTCGCACGGGCTGAAGTGCAGTGGCGCTATTTCGGCTCACTGCAACCTCTGCCTCCCAGGT CTCTGTCGCACGGGCTGAAGTGCAGTGGCGCTGTTTCGGCTCACTGCAACCTCTGCCTCCCAGGT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs537663907 Functional Loss SNV dbSNP153 33..33 33 - - - 47015 RMVar_ID_47015 Human_SNP_ID_252242528 A-to-I Human chr5 - 134402494 134402491 134402495 GTTTTTTGTTTTTTGTTTTGTTTTTTTGAGACAGAGTCTTGCTCTGTTGCCCAGGCAGTAGTGCA GTTTTTTGTTTTTTGTTTTGTTTTTTTGAGA____GTCTTGCTCTGTTGCCCAGGCAGTAGTGCA CTCTG C CDKN2AIPNL Ensembl:ENSG00000237190 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1179078835 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_7384861,Human_RBP_ID_26529249 47016 RMVar_ID_47016 Human_SNP_ID_252267925 A-to-I Human chr5 + 134508641 134508641 134508641 TTGAGCCCAGAAGGTCGAAGCTGCAGTAAGCCATGGTCATGCCAGCGGAGTTGAGCCTGGACCAC TTGAGCCCAGAAGGTCGAAGCTGCAGTAAGCCGTGGTCATGCCAGCGGAGTTGAGCCTGGACCAC A G LINC01843 Ensembl:ENSG00000251169 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs927766308 Functional Loss SNV dbSNP153 33..33 33 - - - 47017 RMVar_ID_47017 Human_SNP_ID_252294169 A-to-I Human chr5 - 134610955 134610955 134610955 GGAGGCTGAGATGGGACTATGACTTGAGCTCAAGAGTCTGAGGTTGCAGTGAACTAGCCTGGATG GGAGGCTGAGATGGGACTATGACTTGAGCTCAGGAGTCTGAGGTTGCAGTGAACTAGCCTGGATG T C SAR1B Ensembl:ENSG00000152700 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs976755140 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7385131,Human_RBP_ID_15302110 RMVar_hsa_circ_53723,RMVar_hsa_circ_311019 47018 RMVar_ID_47018 Human_SNP_ID_252295794 A-to-I Human chr5 - 134617193 134617193 134617193 GTGTCTCACTCTGTGGCCCAGGCTGGAGTGCAATGGCACAATCGCGGCTCACTGCAGCCTCAACC GTGTCTCACTCTGTGGCCCAGGCTGGAGTGCAGTGGCACAATCGCGGCTCACTGCAGCCTCAACC T C SAR1B Ensembl:ENSG00000152700 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1487979682 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_53723,RMVar_hsa_circ_311019,RMVar_hsa_circ_351434 47019 RMVar_ID_47019 Human_SNP_ID_252298108 A-to-I Human chr5 - 134627130 134627130 134627130 GGAGAATGGCGTGAACCTGGGAGGTGGAGCTTACAGTGAGAGGAGATCGCGCCAGTGCACTCCAT GGAGAATGGCGTGAACCTGGGAGGTGGAGCTTGCAGTGAGAGGAGATCGCGCCAGTGCACTCCAT T C SAR1B Ensembl:ENSG00000152700 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1356378504 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25855663 47020 RMVar_ID_47020 Human_SNP_ID_252302408 A-to-I Human chr5 - 134644164 134644164 134644164 TGGCAGGTGCCTGTAATCCCAGTTACTCGGGAAGCTGAGGCAGAAGAATCATTTGAACCCAGGAG TGGCAGGTGCCTGTAATCCCAGTTACTCGGGAGGCTGAGGCAGAAGAATCATTTGAACCCAGGAG T C SAR1B Ensembl:ENSG00000152700 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1320290469 Functional Loss SNV dbSNP153 33..33 33 - - - 47021 RMVar_ID_47021 Human_SNP_ID_252302665 A-to-I Human chr5 - 134645343 134645343 134645343 TTGAGGAGAGCTGGGCATGGTGGCTCACGCCTATAATCCCAGGACTTTGGGAGGCCAAGGCAAGT TTGAGGAGAGCTGGGCATGGTGGCTCACGCCTGTAATCCCAGGACTTTGGGAGGCCAAGGCAAGT T C SAR1B Ensembl:ENSG00000152700 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs543776223 Functional Loss SNV dbSNP153 33..33 33 - - - 47022 RMVar_ID_47022 Human_SNP_ID_252304849 A-to-I Human chr5 + 134654092 134654091 134654092 GAGGTAGGAGGATCACCTGTGTCCAGGAGGTTAAGGCTGCAATGAGCCATGATCATGCCACTACC GAGGTAGGAGGATCACCTGTGTCCAGGAGGTT_AGGCTGCAATGAGCCATGATCATGCCACTACC TA T SEC24A Ensembl:ENSG00000113615 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs540448554 Functional Loss DEL dbSNP153 33..33 33 - - - 47023 RMVar_ID_47023 Human_SNP_ID_252305087 A-to-I Human chr5 + 134655005 134655005 134655005 CCAAAGTGCTGGGATTACAGGTGTGAACCACTACGCCTGGCCCAGGCTTTCCTAAAGAAACGTAC CCAAAGTGCTGGGATTACAGGTGTGAACCACTCCGCCTGGCCCAGGCTTTCCTAAAGAAACGTAC A C SEC24A Ensembl:ENSG00000113615 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4958257 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5780,GWAS_ID_5781,GWAS_ID_5782 47024 RMVar_ID_47024 Human_SNP_ID_252305088 A-to-I Human chr5 + 134655005 134655005 134655005 CCAAAGTGCTGGGATTACAGGTGTGAACCACTACGCCTGGCCCAGGCTTTCCTAAAGAAACGTAC CCAAAGTGCTGGGATTACAGGTGTGAACCACTGCGCCTGGCCCAGGCTTTCCTAAAGAAACGTAC A G SEC24A Ensembl:ENSG00000113615 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4958257 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5780,GWAS_ID_5781,GWAS_ID_5782 47025 RMVar_ID_47025 Human_SNP_ID_252305501 A-to-I Human chr5 + 134656610 134656610 134656610 TTCAAGCAATTCTCCTGCCTCAGCCTCTGAGTAGCTGGGACTATAGGCGTGTGCCACCATGCCCG TTCAAGCAATTCTCCTGCCTCAGCCTCTGAGTGGCTGGGACTATAGGCGTGTGCCACCATGCCCG A G SEC24A Ensembl:ENSG00000113615 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1161246005 Functional Loss SNV dbSNP153 33..33 33 - - - 47026 RMVar_ID_47026 Human_SNP_ID_252305905 A-to-I Human chr5 + 134658177 134658177 134658177 TAATCCTAGCTACTCGAGAGGCTGAATGAGGCAGGAGAATCGCCTGAACCCAGGAGGCGGAGGTT TAATCCTAGCTACTCGAGAGGCTGAATGAGGCGGGAGAATCGCCTGAACCCAGGAGGCGGAGGTT A G SEC24A Ensembl:ENSG00000113615 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1035466786 Functional Loss SNV dbSNP153 33..33 33 - - - 47027 RMVar_ID_47027 Human_SNP_ID_252305992 A-to-I Human chr5 + 134658544 134658544 134658544 CCTCAGCCTCCTGAGAAGCTAGATCTACAGGCATGTGCCACAACTCCTGGCTAATTTTTTAATTT CCTCAGCCTCCTGAGAAGCTAGATCTACAGGCGTGTGCCACAACTCCTGGCTAATTTTTTAATTT A G SEC24A Ensembl:ENSG00000113615 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs150029790 Functional Loss SNV dbSNP153 33..33 33 - - - 47028 RMVar_ID_47028 Human_SNP_ID_252306755 A-to-I Human chr5 + 134661342 134661342 134661342 ACACCTTCGCTTCATAGTGGTCCTGCTCCCCGAATGCCATTACCTGCTTCTCAGAACCCAGCTAC ACACCTTCGCTTCATAGTGGTCCTGCTCCCCGCATGCCATTACCTGCTTCTCAGAACCCAGCTAC A C SEC24A Ensembl:ENSG00000113615 Protein coding CDS GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs138041593 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_74687,Human_RBP_ID_840103,Human_RBP_ID_17302319,Human_RBP_ID_17415343,Human_RBP_ID_22100172 RMVar_hsa_circ_63156,RMVar_hsa_circ_274213,RMVar_hsa_circ_352721,RMVar_hsa_circ_367561,RMVar_hsa_circ_378425,RMVar_hsa_circ_366335,RMVar_hsa_circ_350306,RMVar_hsa_circ_119701,RMVar_hsa_circ_123001,RMVar_hsa_circ_100845,RMVar_hsa_circ_234524,RMVar_hsa_circ_234526,RMVar_hsa_circ_234527,RMVar_hsa_circ_234528,RMVar_hsa_circ_234525,RMVar_hsa_circ_234523 47029 RMVar_ID_47029 Human_SNP_ID_252308011 A-to-I Human chr5 + 134666434 134666434 134666434 AAAAAATTCACCGGGCATGGTTTCACATGCCTATAGTCCCTCCTACTCAGGAGGCTGAGGCAGGG AAAAAATTCACCGGGCATGGTTTCACATGCCTGTAGTCCCTCCTACTCAGGAGGCTGAGGCAGGG A G SEC24A Ensembl:ENSG00000113615 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1235723293 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63156,RMVar_hsa_circ_352721,RMVar_hsa_circ_367561,RMVar_hsa_circ_378425,RMVar_hsa_circ_366335,RMVar_hsa_circ_350306,RMVar_hsa_circ_119701,RMVar_hsa_circ_123001,RMVar_hsa_circ_100845,RMVar_hsa_circ_234524,RMVar_hsa_circ_234526,RMVar_hsa_circ_234527,RMVar_hsa_circ_234528,RMVar_hsa_circ_234525 47030 RMVar_ID_47030 Human_SNP_ID_252309231 A-to-I Human chr5 + 134671476 134671476 134671476 CTGCTGAAATCTTTCAGATGGTATATAATTTTATAAACTTCATAAAGAACCATCTTTTGCTAGAA CTGCTGAAATCTTTCAGATGGTATATAATTTTGTAAACTTCATAAAGAACCATCTTTTGCTAGAA A G SEC24A Ensembl:ENSG00000113615 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4958263 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5783,GWAS_ID_5784,GWAS_ID_5785,GWAS_ID_5786,GWAS_ID_5787,GWAS_ID_5788 RMVar_hsa_circ_63156,RMVar_hsa_circ_352721,RMVar_hsa_circ_367561,RMVar_hsa_circ_378425,RMVar_hsa_circ_366335,RMVar_hsa_circ_119701,RMVar_hsa_circ_123001,RMVar_hsa_circ_100845,RMVar_hsa_circ_234533,RMVar_hsa_circ_90206,RMVar_hsa_circ_234524,RMVar_hsa_circ_234526,RMVar_hsa_circ_234527,RMVar_hsa_circ_234528,RMVar_hsa_circ_234525,RMVar_hsa_circ_316928,RMVar_hsa_circ_346380,RMVar_hsa_circ_374082,RMVar_hsa_circ_372661,RMVar_hsa_circ_324268,RMVar_hsa_circ_115390,RMVar_hsa_circ_278363,RMVar_hsa_circ_110619,RMVar_hsa_circ_86291,RMVar_hsa_circ_234535,RMVar_hsa_circ_234537,RMVar_hsa_circ_234538,RMVar_hsa_circ_234536,RMVar_hsa_circ_234534,RMVar_hsa_circ_234529,RMVar_hsa_circ_234531,RMVar_hsa_circ_234532,RMVar_hsa_circ_234530 47031 RMVar_ID_47031 Human_SNP_ID_252309669 A-to-I Human chr5 + 134673185 134673185 134673185 TCAAGCGATTCTCCTGCCTCAGCTTCCCGAGTAGCTGGGATTACAGGCACGTGCCACCACGCCCA TCAAGCGATTCTCCTGCCTCAGCTTCCCGAGTTGCTGGGATTACAGGCACGTGCCACCACGCCCA A T SEC24A Ensembl:ENSG00000113615 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1246110270 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23153,RMVar_hsa_circ_63156,RMVar_hsa_circ_367561,RMVar_hsa_circ_378425,RMVar_hsa_circ_366335,RMVar_hsa_circ_119701,RMVar_hsa_circ_123001,RMVar_hsa_circ_100845,RMVar_hsa_circ_234533,RMVar_hsa_circ_90206,RMVar_hsa_circ_234524,RMVar_hsa_circ_234526,RMVar_hsa_circ_234527,RMVar_hsa_circ_234528,RMVar_hsa_circ_234525,RMVar_hsa_circ_316928,RMVar_hsa_circ_346380,RMVar_hsa_circ_374082,RMVar_hsa_circ_372661,RMVar_hsa_circ_324268,RMVar_hsa_circ_115390,RMVar_hsa_circ_110619,RMVar_hsa_circ_86291,RMVar_hsa_circ_234535,RMVar_hsa_circ_234537,RMVar_hsa_circ_234536,RMVar_hsa_circ_234534,RMVar_hsa_circ_234529,RMVar_hsa_circ_234531,RMVar_hsa_circ_234532,RMVar_hsa_circ_234530,RMVar_hsa_circ_303626,RMVar_hsa_circ_337937,RMVar_hsa_circ_366850,RMVar_hsa_circ_378363,RMVar_hsa_circ_340580,RMVar_hsa_circ_336004,RMVar_hsa_circ_105485,RMVar_hsa_circ_25480,RMVar_hsa_circ_234541,RMVar_hsa_circ_234542,RMVar_hsa_circ_234543,RMVar_hsa_circ_234540 47032 RMVar_ID_47032 Human_SNP_ID_252309767 A-to-I Human chr5 + 134673575 134673575 134673575 CACCTCCTGGATTCAAGCAGTTCTACCACCTCAGCCTCTCAAGTAGCTGGAACTACAGGCACATG CACCTCCTGGATTCAAGCAGTTCTACCACCTCGGCCTCTCAAGTAGCTGGAACTACAGGCACATG A G SEC24A Ensembl:ENSG00000113615 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1428160662 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23153,RMVar_hsa_circ_63156,RMVar_hsa_circ_367561,RMVar_hsa_circ_378425,RMVar_hsa_circ_366335,RMVar_hsa_circ_119701,RMVar_hsa_circ_123001,RMVar_hsa_circ_100845,RMVar_hsa_circ_234533,RMVar_hsa_circ_90206,RMVar_hsa_circ_234524,RMVar_hsa_circ_234526,RMVar_hsa_circ_234527,RMVar_hsa_circ_234528,RMVar_hsa_circ_234525,RMVar_hsa_circ_316928,RMVar_hsa_circ_346380,RMVar_hsa_circ_374082,RMVar_hsa_circ_372661,RMVar_hsa_circ_324268,RMVar_hsa_circ_115390,RMVar_hsa_circ_110619,RMVar_hsa_circ_86291,RMVar_hsa_circ_234535,RMVar_hsa_circ_234537,RMVar_hsa_circ_234536,RMVar_hsa_circ_234534,RMVar_hsa_circ_234529,RMVar_hsa_circ_234531,RMVar_hsa_circ_234532,RMVar_hsa_circ_234530,RMVar_hsa_circ_303626,RMVar_hsa_circ_337937,RMVar_hsa_circ_366850,RMVar_hsa_circ_378363,RMVar_hsa_circ_340580,RMVar_hsa_circ_336004,RMVar_hsa_circ_105485,RMVar_hsa_circ_25480,RMVar_hsa_circ_234541,RMVar_hsa_circ_234542,RMVar_hsa_circ_234543,RMVar_hsa_circ_234540 47033 RMVar_ID_47033 Human_SNP_ID_252309774 A-to-I Human chr5 + 134673597 134673597 134673597 CTACCACCTCAGCCTCTCAAGTAGCTGGAACTACAGGCACATGCCACCACATCTGGGTAATTTTT CTACCACCTCAGCCTCTCAAGTAGCTGGAACTGCAGGCACATGCCACCACATCTGGGTAATTTTT A G SEC24A Ensembl:ENSG00000113615 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1422745162 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23153,RMVar_hsa_circ_63156,RMVar_hsa_circ_367561,RMVar_hsa_circ_378425,RMVar_hsa_circ_366335,RMVar_hsa_circ_119701,RMVar_hsa_circ_123001,RMVar_hsa_circ_100845,RMVar_hsa_circ_234533,RMVar_hsa_circ_90206,RMVar_hsa_circ_234524,RMVar_hsa_circ_234526,RMVar_hsa_circ_234527,RMVar_hsa_circ_234528,RMVar_hsa_circ_234525,RMVar_hsa_circ_316928,RMVar_hsa_circ_346380,RMVar_hsa_circ_374082,RMVar_hsa_circ_372661,RMVar_hsa_circ_324268,RMVar_hsa_circ_115390,RMVar_hsa_circ_110619,RMVar_hsa_circ_86291,RMVar_hsa_circ_234535,RMVar_hsa_circ_234537,RMVar_hsa_circ_234536,RMVar_hsa_circ_234534,RMVar_hsa_circ_234529,RMVar_hsa_circ_234531,RMVar_hsa_circ_234532,RMVar_hsa_circ_234530,RMVar_hsa_circ_303626,RMVar_hsa_circ_337937,RMVar_hsa_circ_366850,RMVar_hsa_circ_378363,RMVar_hsa_circ_340580,RMVar_hsa_circ_336004,RMVar_hsa_circ_105485,RMVar_hsa_circ_25480,RMVar_hsa_circ_234541,RMVar_hsa_circ_234542,RMVar_hsa_circ_234543,RMVar_hsa_circ_234540 47034 RMVar_ID_47034 Human_SNP_ID_252309795 A-to-I Human chr5 + 134673668 134673668 134673668 TTTAGTAGTGATGGGATTTCACTGTGTTGGCCAGGCTGGTCTCCAACTCCTGACCTCAAAGTGAT TTTAGTAGTGATGGGATTTCACTGTGTTGGCCGGGCTGGTCTCCAACTCCTGACCTCAAAGTGAT A G SEC24A Ensembl:ENSG00000113615 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1289549526 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23153,RMVar_hsa_circ_63156,RMVar_hsa_circ_367561,RMVar_hsa_circ_378425,RMVar_hsa_circ_366335,RMVar_hsa_circ_119701,RMVar_hsa_circ_123001,RMVar_hsa_circ_100845,RMVar_hsa_circ_234533,RMVar_hsa_circ_90206,RMVar_hsa_circ_234524,RMVar_hsa_circ_234526,RMVar_hsa_circ_234527,RMVar_hsa_circ_234528,RMVar_hsa_circ_234525,RMVar_hsa_circ_316928,RMVar_hsa_circ_346380,RMVar_hsa_circ_374082,RMVar_hsa_circ_372661,RMVar_hsa_circ_324268,RMVar_hsa_circ_115390,RMVar_hsa_circ_110619,RMVar_hsa_circ_86291,RMVar_hsa_circ_234535,RMVar_hsa_circ_234537,RMVar_hsa_circ_234536,RMVar_hsa_circ_234534,RMVar_hsa_circ_234529,RMVar_hsa_circ_234531,RMVar_hsa_circ_234532,RMVar_hsa_circ_234530,RMVar_hsa_circ_303626,RMVar_hsa_circ_337937,RMVar_hsa_circ_366850,RMVar_hsa_circ_378363,RMVar_hsa_circ_340580,RMVar_hsa_circ_336004,RMVar_hsa_circ_105485,RMVar_hsa_circ_25480,RMVar_hsa_circ_234541,RMVar_hsa_circ_234542,RMVar_hsa_circ_234543,RMVar_hsa_circ_234540 47035 RMVar_ID_47035 Human_SNP_ID_252310713 A-to-I Human chr5 + 134677211 134677211 134677211 AGACCAGCTTAGTCCTGGCTACTCGGGAGGCTAAGGTGGGAGGATCACTTGAGCCCAGGAGGTTG AGACCAGCTTAGTCCTGGCTACTCGGGAGGCTGAGGTGGGAGGATCACTTGAGCCCAGGAGGTTG A G SEC24A Ensembl:ENSG00000113615 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1346929804 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63156,RMVar_hsa_circ_367561,RMVar_hsa_circ_378425,RMVar_hsa_circ_366335,RMVar_hsa_circ_119701,RMVar_hsa_circ_123001,RMVar_hsa_circ_100845,RMVar_hsa_circ_234533,RMVar_hsa_circ_90206,RMVar_hsa_circ_234524,RMVar_hsa_circ_234526,RMVar_hsa_circ_234527,RMVar_hsa_circ_234528,RMVar_hsa_circ_234525,RMVar_hsa_circ_316928,RMVar_hsa_circ_374082,RMVar_hsa_circ_372661,RMVar_hsa_circ_324268,RMVar_hsa_circ_115390,RMVar_hsa_circ_110619,RMVar_hsa_circ_86291,RMVar_hsa_circ_234535,RMVar_hsa_circ_234536,RMVar_hsa_circ_234534,RMVar_hsa_circ_234529,RMVar_hsa_circ_234531,RMVar_hsa_circ_234532,RMVar_hsa_circ_234530,RMVar_hsa_circ_337937,RMVar_hsa_circ_366850,RMVar_hsa_circ_378363,RMVar_hsa_circ_340580,RMVar_hsa_circ_336004,RMVar_hsa_circ_105485,RMVar_hsa_circ_25480,RMVar_hsa_circ_83820,RMVar_hsa_circ_24133,RMVar_hsa_circ_234541,RMVar_hsa_circ_234542,RMVar_hsa_circ_234543,RMVar_hsa_circ_294529,RMVar_hsa_circ_320918,RMVar_hsa_circ_347453,RMVar_hsa_circ_362704,RMVar_hsa_circ_322834,RMVar_hsa_circ_304369,RMVar_hsa_circ_280706,RMVar_hsa_circ_28989,RMVar_hsa_circ_234546,RMVar_hsa_circ_234548,RMVar_hsa_circ_13208,RMVar_hsa_circ_234547,RMVar_hsa_circ_234544,RMVar_hsa_circ_234545,RMVar_hsa_circ_86864,RMVar_hsa_circ_49527,RMVar_hsa_circ_103204,RMVar_hsa_circ_234550,RMVar_hsa_circ_234551,RMVar_hsa_circ_234552,RMVar_hsa_circ_369767,RMVar_hsa_circ_55900,RMVar_hsa_circ_234553 47036 RMVar_ID_47036 Human_SNP_ID_252310849 A-to-I Human chr5 + 134677672 134677672 134677672 CCAGCCTGGCCAACGTGGTGAAACTCGTCTCTACCAGAAATAGAAAATTTAGCCAAGCATGGTGA CCAGCCTGGCCAACGTGGTGAAACTCGTCTCTTCCAGAAATAGAAAATTTAGCCAAGCATGGTGA A T SEC24A Ensembl:ENSG00000113615 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1226759753 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63156,RMVar_hsa_circ_367561,RMVar_hsa_circ_378425,RMVar_hsa_circ_366335,RMVar_hsa_circ_119701,RMVar_hsa_circ_123001,RMVar_hsa_circ_100845,RMVar_hsa_circ_234533,RMVar_hsa_circ_90206,RMVar_hsa_circ_234524,RMVar_hsa_circ_234526,RMVar_hsa_circ_234527,RMVar_hsa_circ_234528,RMVar_hsa_circ_234525,RMVar_hsa_circ_316928,RMVar_hsa_circ_374082,RMVar_hsa_circ_372661,RMVar_hsa_circ_324268,RMVar_hsa_circ_115390,RMVar_hsa_circ_110619,RMVar_hsa_circ_86291,RMVar_hsa_circ_234535,RMVar_hsa_circ_234536,RMVar_hsa_circ_234534,RMVar_hsa_circ_234529,RMVar_hsa_circ_234531,RMVar_hsa_circ_234532,RMVar_hsa_circ_234530,RMVar_hsa_circ_337937,RMVar_hsa_circ_366850,RMVar_hsa_circ_378363,RMVar_hsa_circ_340580,RMVar_hsa_circ_336004,RMVar_hsa_circ_105485,RMVar_hsa_circ_25480,RMVar_hsa_circ_83820,RMVar_hsa_circ_24133,RMVar_hsa_circ_234541,RMVar_hsa_circ_234542,RMVar_hsa_circ_234543,RMVar_hsa_circ_294529,RMVar_hsa_circ_320918,RMVar_hsa_circ_347453,RMVar_hsa_circ_362704,RMVar_hsa_circ_322834,RMVar_hsa_circ_304369,RMVar_hsa_circ_280706,RMVar_hsa_circ_28989,RMVar_hsa_circ_234546,RMVar_hsa_circ_234548,RMVar_hsa_circ_13208,RMVar_hsa_circ_234547,RMVar_hsa_circ_234544,RMVar_hsa_circ_234545,RMVar_hsa_circ_86864,RMVar_hsa_circ_49527,RMVar_hsa_circ_103204,RMVar_hsa_circ_234550,RMVar_hsa_circ_234551,RMVar_hsa_circ_234552,RMVar_hsa_circ_369767,RMVar_hsa_circ_55900,RMVar_hsa_circ_234553 47037 RMVar_ID_47037 Human_SNP_ID_252310950 A-to-I Human chr5 + 134678070 134678070 134678070 TAGAGACCGGGTCTCTCGTTGTCACCCAGGTTAGAGTGCAGTTCCATGATCATAGCTCACTGCAG TAGAGACCGGGTCTCTCGTTGTCACCCAGGTTGGAGTGCAGTTCCATGATCATAGCTCACTGCAG A G SEC24A Ensembl:ENSG00000113615 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053062329 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18832532 RMVar_hsa_circ_63156,RMVar_hsa_circ_367561,RMVar_hsa_circ_378425,RMVar_hsa_circ_366335,RMVar_hsa_circ_119701,RMVar_hsa_circ_123001,RMVar_hsa_circ_100845,RMVar_hsa_circ_234533,RMVar_hsa_circ_90206,RMVar_hsa_circ_234524,RMVar_hsa_circ_234526,RMVar_hsa_circ_234527,RMVar_hsa_circ_234528,RMVar_hsa_circ_234525,RMVar_hsa_circ_316928,RMVar_hsa_circ_374082,RMVar_hsa_circ_372661,RMVar_hsa_circ_324268,RMVar_hsa_circ_115390,RMVar_hsa_circ_110619,RMVar_hsa_circ_86291,RMVar_hsa_circ_234535,RMVar_hsa_circ_234536,RMVar_hsa_circ_234534,RMVar_hsa_circ_234529,RMVar_hsa_circ_234531,RMVar_hsa_circ_234532,RMVar_hsa_circ_234530,RMVar_hsa_circ_337937,RMVar_hsa_circ_366850,RMVar_hsa_circ_378363,RMVar_hsa_circ_340580,RMVar_hsa_circ_336004,RMVar_hsa_circ_105485,RMVar_hsa_circ_25480,RMVar_hsa_circ_83820,RMVar_hsa_circ_24133,RMVar_hsa_circ_234541,RMVar_hsa_circ_234542,RMVar_hsa_circ_234543,RMVar_hsa_circ_294529,RMVar_hsa_circ_320918,RMVar_hsa_circ_347453,RMVar_hsa_circ_362704,RMVar_hsa_circ_322834,RMVar_hsa_circ_304369,RMVar_hsa_circ_280706,RMVar_hsa_circ_28989,RMVar_hsa_circ_234546,RMVar_hsa_circ_234548,RMVar_hsa_circ_13208,RMVar_hsa_circ_234547,RMVar_hsa_circ_234544,RMVar_hsa_circ_234545,RMVar_hsa_circ_86864,RMVar_hsa_circ_49527,RMVar_hsa_circ_103204,RMVar_hsa_circ_234550,RMVar_hsa_circ_234551,RMVar_hsa_circ_234552,RMVar_hsa_circ_369767,RMVar_hsa_circ_55900,RMVar_hsa_circ_234553 47038 RMVar_ID_47038 Human_SNP_ID_252311643 A-to-I Human chr5 + 134680976 134680976 134680976 CAATAATTAGCCGGGTGTGGTGGCGGGCACCTATAATCCCAGCTACTCGGGAGGCTGAGGCAGGA CAATAATTAGCCGGGTGTGGTGGCGGGCACCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGA A G SEC24A Ensembl:ENSG00000113615 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1342111286 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63156,RMVar_hsa_circ_367561,RMVar_hsa_circ_366335,RMVar_hsa_circ_119701,RMVar_hsa_circ_123001,RMVar_hsa_circ_100845,RMVar_hsa_circ_234533,RMVar_hsa_circ_90206,RMVar_hsa_circ_234524,RMVar_hsa_circ_234526,RMVar_hsa_circ_234527,RMVar_hsa_circ_234528,RMVar_hsa_circ_234525,RMVar_hsa_circ_316928,RMVar_hsa_circ_374082,RMVar_hsa_circ_372661,RMVar_hsa_circ_115390,RMVar_hsa_circ_110619,RMVar_hsa_circ_86291,RMVar_hsa_circ_234535,RMVar_hsa_circ_234534,RMVar_hsa_circ_234529,RMVar_hsa_circ_234531,RMVar_hsa_circ_234532,RMVar_hsa_circ_234530,RMVar_hsa_circ_337937,RMVar_hsa_circ_366850,RMVar_hsa_circ_378363,RMVar_hsa_circ_340580,RMVar_hsa_circ_105485,RMVar_hsa_circ_25480,RMVar_hsa_circ_83820,RMVar_hsa_circ_24133,RMVar_hsa_circ_234542,RMVar_hsa_circ_234543,RMVar_hsa_circ_294529,RMVar_hsa_circ_347453,RMVar_hsa_circ_362704,RMVar_hsa_circ_322834,RMVar_hsa_circ_304369,RMVar_hsa_circ_280706,RMVar_hsa_circ_28989,RMVar_hsa_circ_234546,RMVar_hsa_circ_13208,RMVar_hsa_circ_234547,RMVar_hsa_circ_234544,RMVar_hsa_circ_234545,RMVar_hsa_circ_86864,RMVar_hsa_circ_49527,RMVar_hsa_circ_103204,RMVar_hsa_circ_234550,RMVar_hsa_circ_234551,RMVar_hsa_circ_234552,RMVar_hsa_circ_369767,RMVar_hsa_circ_55900,RMVar_hsa_circ_44677,RMVar_hsa_circ_115121,RMVar_hsa_circ_338506,RMVar_hsa_circ_234553,RMVar_hsa_circ_355590,RMVar_hsa_circ_287636,RMVar_hsa_circ_68346,RMVar_hsa_circ_234554,RMVar_hsa_circ_234556,RMVar_hsa_circ_234557,RMVar_hsa_circ_234555 47039 RMVar_ID_47039 Human_SNP_ID_252312143 A-to-I Human chr5 + 134682756 134682755 134682757 ACCACCACACCTGGCTTATTTTTATTAGAGACAGAGTTTTGCTATGTTGCCCAGGCTGGTCTCGA ACCACCACACCTGGCTTATTTTTATTAGAGAC__AGTTTTGCTATGTTGCCCAGGCTGGTCTCGA CAG C SEC24A Ensembl:ENSG00000113615 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1396880077 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_63156,RMVar_hsa_circ_367561,RMVar_hsa_circ_119701,RMVar_hsa_circ_123001,RMVar_hsa_circ_100845,RMVar_hsa_circ_234533,RMVar_hsa_circ_90206,RMVar_hsa_circ_234524,RMVar_hsa_circ_234526,RMVar_hsa_circ_234527,RMVar_hsa_circ_234528,RMVar_hsa_circ_234525,RMVar_hsa_circ_374082,RMVar_hsa_circ_372661,RMVar_hsa_circ_115390,RMVar_hsa_circ_110619,RMVar_hsa_circ_86291,RMVar_hsa_circ_234534,RMVar_hsa_circ_234529,RMVar_hsa_circ_234531,RMVar_hsa_circ_234532,RMVar_hsa_circ_234530,RMVar_hsa_circ_366850,RMVar_hsa_circ_378363,RMVar_hsa_circ_340580,RMVar_hsa_circ_105485,RMVar_hsa_circ_25480,RMVar_hsa_circ_33135,RMVar_hsa_circ_83820,RMVar_hsa_circ_24133,RMVar_hsa_circ_234543,RMVar_hsa_circ_347453,RMVar_hsa_circ_362704,RMVar_hsa_circ_322834,RMVar_hsa_circ_304369,RMVar_hsa_circ_280706,RMVar_hsa_circ_28989,RMVar_hsa_circ_234546,RMVar_hsa_circ_13208,RMVar_hsa_circ_234544,RMVar_hsa_circ_234545,RMVar_hsa_circ_86864,RMVar_hsa_circ_103204,RMVar_hsa_circ_234550,RMVar_hsa_circ_234551,RMVar_hsa_circ_234552,RMVar_hsa_circ_369767,RMVar_hsa_circ_55900,RMVar_hsa_circ_44677,RMVar_hsa_circ_115121,RMVar_hsa_circ_338506,RMVar_hsa_circ_234553,RMVar_hsa_circ_355590,RMVar_hsa_circ_68346,RMVar_hsa_circ_234554,RMVar_hsa_circ_234556,RMVar_hsa_circ_234557,RMVar_hsa_circ_234555,RMVar_hsa_circ_300242,RMVar_hsa_circ_341964,RMVar_hsa_circ_370025,RMVar_hsa_circ_312683,RMVar_hsa_circ_58221,RMVar_hsa_circ_234558,RMVar_hsa_circ_234559,RMVar_hsa_circ_234560 47040 RMVar_ID_47040 Human_SNP_ID_252312315 A-to-I Human chr5 + 134683545 134683545 134683545 TAACGTTTATTTCTTTTAGAGAGGAGGGTCTTACTTTGTTGCTGAAGCTAAAGTGCAGTGGCACT TAACGTTTATTTCTTTTAGAGAGGAGGGTCTTGCTTTGTTGCTGAAGCTAAAGTGCAGTGGCACT A G SEC24A Ensembl:ENSG00000113615 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1028888119 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15302564 RMVar_hsa_circ_63156,RMVar_hsa_circ_367561,RMVar_hsa_circ_119701,RMVar_hsa_circ_123001,RMVar_hsa_circ_100845,RMVar_hsa_circ_234533,RMVar_hsa_circ_90206,RMVar_hsa_circ_234524,RMVar_hsa_circ_234526,RMVar_hsa_circ_234527,RMVar_hsa_circ_234528,RMVar_hsa_circ_234525,RMVar_hsa_circ_374082,RMVar_hsa_circ_372661,RMVar_hsa_circ_115390,RMVar_hsa_circ_110619,RMVar_hsa_circ_86291,RMVar_hsa_circ_234534,RMVar_hsa_circ_234529,RMVar_hsa_circ_234531,RMVar_hsa_circ_234532,RMVar_hsa_circ_234530,RMVar_hsa_circ_366850,RMVar_hsa_circ_378363,RMVar_hsa_circ_340580,RMVar_hsa_circ_105485,RMVar_hsa_circ_25480,RMVar_hsa_circ_33135,RMVar_hsa_circ_83820,RMVar_hsa_circ_24133,RMVar_hsa_circ_234543,RMVar_hsa_circ_347453,RMVar_hsa_circ_362704,RMVar_hsa_circ_322834,RMVar_hsa_circ_304369,RMVar_hsa_circ_280706,RMVar_hsa_circ_28989,RMVar_hsa_circ_234546,RMVar_hsa_circ_13208,RMVar_hsa_circ_234544,RMVar_hsa_circ_234545,RMVar_hsa_circ_86864,RMVar_hsa_circ_103204,RMVar_hsa_circ_234550,RMVar_hsa_circ_234551,RMVar_hsa_circ_234552,RMVar_hsa_circ_369767,RMVar_hsa_circ_55900,RMVar_hsa_circ_44677,RMVar_hsa_circ_115121,RMVar_hsa_circ_338506,RMVar_hsa_circ_234553,RMVar_hsa_circ_355590,RMVar_hsa_circ_68346,RMVar_hsa_circ_234554,RMVar_hsa_circ_234556,RMVar_hsa_circ_234557,RMVar_hsa_circ_234555,RMVar_hsa_circ_300242,RMVar_hsa_circ_341964,RMVar_hsa_circ_370025,RMVar_hsa_circ_312683,RMVar_hsa_circ_58221,RMVar_hsa_circ_234558,RMVar_hsa_circ_234559,RMVar_hsa_circ_234560 47041 RMVar_ID_47041 Human_SNP_ID_252312332 A-to-I Human chr5 + 134683653 134683653 134683653 CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGACATGCACCACCATGCCCTGCTAATTTTT CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTGCAGACATGCACCACCATGCCCTGCTAATTTTT A G SEC24A Ensembl:ENSG00000113615 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1561815774 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63156,RMVar_hsa_circ_367561,RMVar_hsa_circ_119701,RMVar_hsa_circ_123001,RMVar_hsa_circ_100845,RMVar_hsa_circ_234533,RMVar_hsa_circ_90206,RMVar_hsa_circ_234524,RMVar_hsa_circ_234526,RMVar_hsa_circ_234527,RMVar_hsa_circ_234528,RMVar_hsa_circ_234525,RMVar_hsa_circ_374082,RMVar_hsa_circ_372661,RMVar_hsa_circ_115390,RMVar_hsa_circ_110619,RMVar_hsa_circ_86291,RMVar_hsa_circ_234534,RMVar_hsa_circ_234529,RMVar_hsa_circ_234531,RMVar_hsa_circ_234532,RMVar_hsa_circ_234530,RMVar_hsa_circ_366850,RMVar_hsa_circ_378363,RMVar_hsa_circ_340580,RMVar_hsa_circ_105485,RMVar_hsa_circ_25480,RMVar_hsa_circ_33135,RMVar_hsa_circ_83820,RMVar_hsa_circ_24133,RMVar_hsa_circ_234543,RMVar_hsa_circ_347453,RMVar_hsa_circ_362704,RMVar_hsa_circ_322834,RMVar_hsa_circ_304369,RMVar_hsa_circ_280706,RMVar_hsa_circ_28989,RMVar_hsa_circ_234546,RMVar_hsa_circ_13208,RMVar_hsa_circ_234544,RMVar_hsa_circ_234545,RMVar_hsa_circ_86864,RMVar_hsa_circ_103204,RMVar_hsa_circ_234550,RMVar_hsa_circ_234551,RMVar_hsa_circ_234552,RMVar_hsa_circ_369767,RMVar_hsa_circ_55900,RMVar_hsa_circ_44677,RMVar_hsa_circ_115121,RMVar_hsa_circ_338506,RMVar_hsa_circ_234553,RMVar_hsa_circ_355590,RMVar_hsa_circ_68346,RMVar_hsa_circ_234554,RMVar_hsa_circ_234556,RMVar_hsa_circ_234557,RMVar_hsa_circ_234555,RMVar_hsa_circ_300242,RMVar_hsa_circ_341964,RMVar_hsa_circ_370025,RMVar_hsa_circ_312683,RMVar_hsa_circ_58221,RMVar_hsa_circ_234558,RMVar_hsa_circ_234559,RMVar_hsa_circ_234560 47042 RMVar_ID_47042 Human_SNP_ID_252312707 A-to-I Human chr5 + 134685240 134685240 134685240 AAAAAATTTCAGGAATTGTGGTGTGTGCTTATAGTCCCAGGTACTTGGGAGGCTGAGGTGGAAGG AAAAAATTTCAGGAATTGTGGTGTGTGCTTATGGTCCCAGGTACTTGGGAGGCTGAGGTGGAAGG A G SEC24A Ensembl:ENSG00000113615 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs944839948 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63156,RMVar_hsa_circ_367561,RMVar_hsa_circ_119701,RMVar_hsa_circ_123001,RMVar_hsa_circ_100845,RMVar_hsa_circ_234533,RMVar_hsa_circ_90206,RMVar_hsa_circ_234524,RMVar_hsa_circ_234526,RMVar_hsa_circ_234527,RMVar_hsa_circ_234528,RMVar_hsa_circ_234525,RMVar_hsa_circ_374082,RMVar_hsa_circ_372661,RMVar_hsa_circ_115390,RMVar_hsa_circ_110619,RMVar_hsa_circ_86291,RMVar_hsa_circ_234534,RMVar_hsa_circ_234529,RMVar_hsa_circ_234531,RMVar_hsa_circ_234532,RMVar_hsa_circ_234530,RMVar_hsa_circ_366850,RMVar_hsa_circ_378363,RMVar_hsa_circ_340580,RMVar_hsa_circ_105485,RMVar_hsa_circ_25480,RMVar_hsa_circ_33135,RMVar_hsa_circ_83820,RMVar_hsa_circ_24133,RMVar_hsa_circ_234543,RMVar_hsa_circ_347453,RMVar_hsa_circ_362704,RMVar_hsa_circ_322834,RMVar_hsa_circ_304369,RMVar_hsa_circ_280706,RMVar_hsa_circ_28989,RMVar_hsa_circ_234546,RMVar_hsa_circ_13208,RMVar_hsa_circ_234544,RMVar_hsa_circ_234545,RMVar_hsa_circ_86864,RMVar_hsa_circ_103204,RMVar_hsa_circ_234550,RMVar_hsa_circ_234551,RMVar_hsa_circ_234552,RMVar_hsa_circ_369767,RMVar_hsa_circ_55900,RMVar_hsa_circ_44677,RMVar_hsa_circ_115121,RMVar_hsa_circ_338506,RMVar_hsa_circ_234553,RMVar_hsa_circ_355590,RMVar_hsa_circ_68346,RMVar_hsa_circ_234554,RMVar_hsa_circ_234556,RMVar_hsa_circ_234557,RMVar_hsa_circ_234555,RMVar_hsa_circ_300242,RMVar_hsa_circ_341964,RMVar_hsa_circ_370025,RMVar_hsa_circ_312683,RMVar_hsa_circ_58221,RMVar_hsa_circ_234558,RMVar_hsa_circ_234559,RMVar_hsa_circ_234560 47043 RMVar_ID_47043 Human_SNP_ID_252312825 A-to-I Human chr5 + 134685722 134685722 134685722 AAATACAGTCTTGGCCAGGTGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCAGCGAA AAATACAGTCTTGGCCAGGTGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCAGCGAA A G SEC24A Ensembl:ENSG00000113615 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs909650713 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63156,RMVar_hsa_circ_367561,RMVar_hsa_circ_119701,RMVar_hsa_circ_123001,RMVar_hsa_circ_100845,RMVar_hsa_circ_234533,RMVar_hsa_circ_90206,RMVar_hsa_circ_234524,RMVar_hsa_circ_234526,RMVar_hsa_circ_234527,RMVar_hsa_circ_234528,RMVar_hsa_circ_234525,RMVar_hsa_circ_374082,RMVar_hsa_circ_372661,RMVar_hsa_circ_115390,RMVar_hsa_circ_110619,RMVar_hsa_circ_86291,RMVar_hsa_circ_234534,RMVar_hsa_circ_234529,RMVar_hsa_circ_234531,RMVar_hsa_circ_234532,RMVar_hsa_circ_234530,RMVar_hsa_circ_366850,RMVar_hsa_circ_378363,RMVar_hsa_circ_340580,RMVar_hsa_circ_105485,RMVar_hsa_circ_25480,RMVar_hsa_circ_33135,RMVar_hsa_circ_83820,RMVar_hsa_circ_24133,RMVar_hsa_circ_234543,RMVar_hsa_circ_347453,RMVar_hsa_circ_362704,RMVar_hsa_circ_322834,RMVar_hsa_circ_304369,RMVar_hsa_circ_280706,RMVar_hsa_circ_28989,RMVar_hsa_circ_234546,RMVar_hsa_circ_13208,RMVar_hsa_circ_234544,RMVar_hsa_circ_234545,RMVar_hsa_circ_86864,RMVar_hsa_circ_103204,RMVar_hsa_circ_234550,RMVar_hsa_circ_234551,RMVar_hsa_circ_234552,RMVar_hsa_circ_369767,RMVar_hsa_circ_55900,RMVar_hsa_circ_44677,RMVar_hsa_circ_115121,RMVar_hsa_circ_338506,RMVar_hsa_circ_234553,RMVar_hsa_circ_355590,RMVar_hsa_circ_68346,RMVar_hsa_circ_234554,RMVar_hsa_circ_234556,RMVar_hsa_circ_234557,RMVar_hsa_circ_234555,RMVar_hsa_circ_300242,RMVar_hsa_circ_341964,RMVar_hsa_circ_370025,RMVar_hsa_circ_312683,RMVar_hsa_circ_58221,RMVar_hsa_circ_234558,RMVar_hsa_circ_234559,RMVar_hsa_circ_234560 47044 RMVar_ID_47044 Human_SNP_ID_252312863 A-to-I Human chr5 + 134685868 134685868 134685868 AAAATTAGCCGGGCGTGGTGGCGCGTGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA AAAATTAGCCGGGCGTGGTGGCGCGTGCCTGTGATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA A G SEC24A Ensembl:ENSG00000113615 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs994093893 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63156,RMVar_hsa_circ_367561,RMVar_hsa_circ_119701,RMVar_hsa_circ_123001,RMVar_hsa_circ_100845,RMVar_hsa_circ_234533,RMVar_hsa_circ_90206,RMVar_hsa_circ_234524,RMVar_hsa_circ_234526,RMVar_hsa_circ_234527,RMVar_hsa_circ_234528,RMVar_hsa_circ_234525,RMVar_hsa_circ_374082,RMVar_hsa_circ_372661,RMVar_hsa_circ_115390,RMVar_hsa_circ_110619,RMVar_hsa_circ_86291,RMVar_hsa_circ_234534,RMVar_hsa_circ_234529,RMVar_hsa_circ_234531,RMVar_hsa_circ_234532,RMVar_hsa_circ_234530,RMVar_hsa_circ_366850,RMVar_hsa_circ_378363,RMVar_hsa_circ_340580,RMVar_hsa_circ_105485,RMVar_hsa_circ_25480,RMVar_hsa_circ_33135,RMVar_hsa_circ_83820,RMVar_hsa_circ_24133,RMVar_hsa_circ_234543,RMVar_hsa_circ_347453,RMVar_hsa_circ_362704,RMVar_hsa_circ_322834,RMVar_hsa_circ_304369,RMVar_hsa_circ_280706,RMVar_hsa_circ_28989,RMVar_hsa_circ_234546,RMVar_hsa_circ_13208,RMVar_hsa_circ_234544,RMVar_hsa_circ_234545,RMVar_hsa_circ_86864,RMVar_hsa_circ_103204,RMVar_hsa_circ_234550,RMVar_hsa_circ_234551,RMVar_hsa_circ_234552,RMVar_hsa_circ_369767,RMVar_hsa_circ_55900,RMVar_hsa_circ_44677,RMVar_hsa_circ_115121,RMVar_hsa_circ_338506,RMVar_hsa_circ_234553,RMVar_hsa_circ_355590,RMVar_hsa_circ_68346,RMVar_hsa_circ_234554,RMVar_hsa_circ_234556,RMVar_hsa_circ_234557,RMVar_hsa_circ_234555,RMVar_hsa_circ_300242,RMVar_hsa_circ_341964,RMVar_hsa_circ_370025,RMVar_hsa_circ_312683,RMVar_hsa_circ_58221,RMVar_hsa_circ_234558,RMVar_hsa_circ_234559,RMVar_hsa_circ_234560 47045 RMVar_ID_47045 Human_SNP_ID_252312966 A-to-I Human chr5 + 134686328 134686328 134686328 ATAATCTCGGCTCACTGCAACCTCCATCTCTCAGGTTCAAGTGATCCTCCTGCCTCAGCCTCCCG ATAATCTCGGCTCACTGCAACCTCCATCTCTCTGGTTCAAGTGATCCTCCTGCCTCAGCCTCCCG A T SEC24A Ensembl:ENSG00000113615 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1308068265 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63156,RMVar_hsa_circ_367561,RMVar_hsa_circ_119701,RMVar_hsa_circ_123001,RMVar_hsa_circ_100845,RMVar_hsa_circ_234533,RMVar_hsa_circ_90206,RMVar_hsa_circ_234524,RMVar_hsa_circ_234526,RMVar_hsa_circ_234527,RMVar_hsa_circ_234528,RMVar_hsa_circ_234525,RMVar_hsa_circ_374082,RMVar_hsa_circ_372661,RMVar_hsa_circ_115390,RMVar_hsa_circ_110619,RMVar_hsa_circ_86291,RMVar_hsa_circ_234534,RMVar_hsa_circ_234529,RMVar_hsa_circ_234531,RMVar_hsa_circ_234532,RMVar_hsa_circ_234530,RMVar_hsa_circ_366850,RMVar_hsa_circ_378363,RMVar_hsa_circ_340580,RMVar_hsa_circ_105485,RMVar_hsa_circ_25480,RMVar_hsa_circ_33135,RMVar_hsa_circ_83820,RMVar_hsa_circ_24133,RMVar_hsa_circ_234543,RMVar_hsa_circ_347453,RMVar_hsa_circ_362704,RMVar_hsa_circ_322834,RMVar_hsa_circ_304369,RMVar_hsa_circ_280706,RMVar_hsa_circ_28989,RMVar_hsa_circ_234546,RMVar_hsa_circ_13208,RMVar_hsa_circ_234544,RMVar_hsa_circ_234545,RMVar_hsa_circ_86864,RMVar_hsa_circ_103204,RMVar_hsa_circ_234550,RMVar_hsa_circ_234551,RMVar_hsa_circ_234552,RMVar_hsa_circ_369767,RMVar_hsa_circ_55900,RMVar_hsa_circ_44677,RMVar_hsa_circ_115121,RMVar_hsa_circ_338506,RMVar_hsa_circ_234553,RMVar_hsa_circ_355590,RMVar_hsa_circ_68346,RMVar_hsa_circ_234554,RMVar_hsa_circ_234556,RMVar_hsa_circ_234557,RMVar_hsa_circ_234555,RMVar_hsa_circ_300242,RMVar_hsa_circ_341964,RMVar_hsa_circ_370025,RMVar_hsa_circ_312683,RMVar_hsa_circ_58221,RMVar_hsa_circ_234558,RMVar_hsa_circ_234559,RMVar_hsa_circ_234560 47046 RMVar_ID_47046 Human_SNP_ID_252312967 A-to-I Human chr5 + 134686334 134686334 134686334 TCGGCTCACTGCAACCTCCATCTCTCAGGTTCAAGTGATCCTCCTGCCTCAGCCTCCCGAGAGTA TCGGCTCACTGCAACCTCCATCTCTCAGGTTCGAGTGATCCTCCTGCCTCAGCCTCCCGAGAGTA A G SEC24A Ensembl:ENSG00000113615 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1221752920 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63156,RMVar_hsa_circ_367561,RMVar_hsa_circ_119701,RMVar_hsa_circ_123001,RMVar_hsa_circ_100845,RMVar_hsa_circ_234533,RMVar_hsa_circ_90206,RMVar_hsa_circ_234524,RMVar_hsa_circ_234526,RMVar_hsa_circ_234527,RMVar_hsa_circ_234528,RMVar_hsa_circ_234525,RMVar_hsa_circ_374082,RMVar_hsa_circ_372661,RMVar_hsa_circ_115390,RMVar_hsa_circ_110619,RMVar_hsa_circ_86291,RMVar_hsa_circ_234534,RMVar_hsa_circ_234529,RMVar_hsa_circ_234531,RMVar_hsa_circ_234532,RMVar_hsa_circ_234530,RMVar_hsa_circ_366850,RMVar_hsa_circ_378363,RMVar_hsa_circ_340580,RMVar_hsa_circ_105485,RMVar_hsa_circ_25480,RMVar_hsa_circ_33135,RMVar_hsa_circ_83820,RMVar_hsa_circ_24133,RMVar_hsa_circ_234543,RMVar_hsa_circ_347453,RMVar_hsa_circ_362704,RMVar_hsa_circ_322834,RMVar_hsa_circ_304369,RMVar_hsa_circ_280706,RMVar_hsa_circ_28989,RMVar_hsa_circ_234546,RMVar_hsa_circ_13208,RMVar_hsa_circ_234544,RMVar_hsa_circ_234545,RMVar_hsa_circ_86864,RMVar_hsa_circ_103204,RMVar_hsa_circ_234550,RMVar_hsa_circ_234551,RMVar_hsa_circ_234552,RMVar_hsa_circ_369767,RMVar_hsa_circ_55900,RMVar_hsa_circ_44677,RMVar_hsa_circ_115121,RMVar_hsa_circ_338506,RMVar_hsa_circ_234553,RMVar_hsa_circ_355590,RMVar_hsa_circ_68346,RMVar_hsa_circ_234554,RMVar_hsa_circ_234556,RMVar_hsa_circ_234557,RMVar_hsa_circ_234555,RMVar_hsa_circ_300242,RMVar_hsa_circ_341964,RMVar_hsa_circ_370025,RMVar_hsa_circ_312683,RMVar_hsa_circ_58221,RMVar_hsa_circ_234558,RMVar_hsa_circ_234559,RMVar_hsa_circ_234560 47047 RMVar_ID_47047 Human_SNP_ID_252313747 A-to-I Human chr5 + 134689708 134689708 134689708 GCGTGAACTCGGGAGGAGGCGGAGCTTGCAGCAAGCCGAGATCGTGCCACCGCACTCCAGCCTGG GCGTGAACTCGGGAGGAGGCGGAGCTTGCAGCGAGCCGAGATCGTGCCACCGCACTCCAGCCTGG A G SEC24A Ensembl:ENSG00000113615 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1249278041 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_63156,RMVar_hsa_circ_119701,RMVar_hsa_circ_123001,RMVar_hsa_circ_100845,RMVar_hsa_circ_234533,RMVar_hsa_circ_90206,RMVar_hsa_circ_234526,RMVar_hsa_circ_234527,RMVar_hsa_circ_234528,RMVar_hsa_circ_234525,RMVar_hsa_circ_372661,RMVar_hsa_circ_115390,RMVar_hsa_circ_110619,RMVar_hsa_circ_86291,RMVar_hsa_circ_234529,RMVar_hsa_circ_234531,RMVar_hsa_circ_234532,RMVar_hsa_circ_234530,RMVar_hsa_circ_366850,RMVar_hsa_circ_378363,RMVar_hsa_circ_105485,RMVar_hsa_circ_25480,RMVar_hsa_circ_33135,RMVar_hsa_circ_83820,RMVar_hsa_circ_24133,RMVar_hsa_circ_234543,RMVar_hsa_circ_347453,RMVar_hsa_circ_362704,RMVar_hsa_circ_322834,RMVar_hsa_circ_280706,RMVar_hsa_circ_28989,RMVar_hsa_circ_13208,RMVar_hsa_circ_234544,RMVar_hsa_circ_234545,RMVar_hsa_circ_86864,RMVar_hsa_circ_103204,RMVar_hsa_circ_234550,RMVar_hsa_circ_234551,RMVar_hsa_circ_234552,RMVar_hsa_circ_369767,RMVar_hsa_circ_44677,RMVar_hsa_circ_115121,RMVar_hsa_circ_338506,RMVar_hsa_circ_234553,RMVar_hsa_circ_68346,RMVar_hsa_circ_234554,RMVar_hsa_circ_234556,RMVar_hsa_circ_234555,RMVar_hsa_circ_341964,RMVar_hsa_circ_370025,RMVar_hsa_circ_312683,RMVar_hsa_circ_58221,RMVar_hsa_circ_41891,RMVar_hsa_circ_309365,RMVar_hsa_circ_234559,RMVar_hsa_circ_234560,RMVar_hsa_circ_327195,RMVar_hsa_circ_327597,RMVar_hsa_circ_341588,RMVar_hsa_circ_309928,RMVar_hsa_circ_301648,RMVar_hsa_circ_46528,RMVar_hsa_circ_72169,RMVar_hsa_circ_234562,RMVar_hsa_circ_234564,RMVar_hsa_circ_234565,RMVar_hsa_circ_234563,RMVar_hsa_circ_234561,RMVar_hsa_circ_360386,RMVar_hsa_circ_56887,RMVar_hsa_circ_62637,RMVar_hsa_circ_39779 47048 RMVar_ID_47048 Human_SNP_ID_252318952 A-to-I Human chr5 + 134709193 134709192 134709194 ATATCGTGCCACTGTACTCCAGCTTGGGTGACAGAGCCAGACTCTGTCTCAAAATAAACAAAAAG ATATCGTGCCACTGTACTCCAGCTTGGGTGAC__AGCCAGACTCTGTCTCAAAATAAACAAAAAG CAG C SEC24A Ensembl:ENSG00000113615 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs754085037 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_123001,RMVar_hsa_circ_100845,RMVar_hsa_circ_234527,RMVar_hsa_circ_234528,RMVar_hsa_circ_115390,RMVar_hsa_circ_234529,RMVar_hsa_circ_105485,RMVar_hsa_circ_25480,RMVar_hsa_circ_79000,RMVar_hsa_circ_83820,RMVar_hsa_circ_24133,RMVar_hsa_circ_234543,RMVar_hsa_circ_234551,RMVar_hsa_circ_28635,RMVar_hsa_circ_41891,RMVar_hsa_circ_46528,RMVar_hsa_circ_39779,RMVar_hsa_circ_331870,RMVar_hsa_circ_286218,RMVar_hsa_circ_117210,RMVar_hsa_circ_234572,RMVar_hsa_circ_234573,RMVar_hsa_circ_360451,RMVar_hsa_circ_234575,RMVar_hsa_circ_353034,RMVar_hsa_circ_234574,RMVar_hsa_circ_342716,RMVar_hsa_circ_234587,RMVar_hsa_circ_120211,RMVar_hsa_circ_234581,RMVar_hsa_circ_355607,RMVar_hsa_circ_234585,RMVar_hsa_circ_51343,RMVar_hsa_circ_356437,RMVar_hsa_circ_284432,RMVar_hsa_circ_299082,RMVar_hsa_circ_234588,RMVar_hsa_circ_234592,RMVar_hsa_circ_295962,RMVar_hsa_circ_332607,RMVar_hsa_circ_272859,RMVar_hsa_circ_324230,RMVar_hsa_circ_234589,RMVar_hsa_circ_338905,RMVar_hsa_circ_276121,RMVar_hsa_circ_234591 47049 RMVar_ID_47049 Human_SNP_ID_252318953 A-to-I Human chr5 + 134709193 134709193 134709193 ATATCGTGCCACTGTACTCCAGCTTGGGTGACAGAGCCAGACTCTGTCTCAAAATAAACAAAAAG ATATCGTGCCACTGTACTCCAGCTTGGGTGACGGAGCCAGACTCTGTCTCAAAATAAACAAAAAG A G SEC24A Ensembl:ENSG00000113615 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1292256808 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123001,RMVar_hsa_circ_100845,RMVar_hsa_circ_234527,RMVar_hsa_circ_234528,RMVar_hsa_circ_115390,RMVar_hsa_circ_234529,RMVar_hsa_circ_105485,RMVar_hsa_circ_25480,RMVar_hsa_circ_79000,RMVar_hsa_circ_83820,RMVar_hsa_circ_24133,RMVar_hsa_circ_234543,RMVar_hsa_circ_234551,RMVar_hsa_circ_28635,RMVar_hsa_circ_41891,RMVar_hsa_circ_46528,RMVar_hsa_circ_39779,RMVar_hsa_circ_331870,RMVar_hsa_circ_286218,RMVar_hsa_circ_117210,RMVar_hsa_circ_234572,RMVar_hsa_circ_234573,RMVar_hsa_circ_360451,RMVar_hsa_circ_234575,RMVar_hsa_circ_353034,RMVar_hsa_circ_234574,RMVar_hsa_circ_342716,RMVar_hsa_circ_234587,RMVar_hsa_circ_120211,RMVar_hsa_circ_234581,RMVar_hsa_circ_355607,RMVar_hsa_circ_234585,RMVar_hsa_circ_51343,RMVar_hsa_circ_356437,RMVar_hsa_circ_284432,RMVar_hsa_circ_299082,RMVar_hsa_circ_234588,RMVar_hsa_circ_234592,RMVar_hsa_circ_295962,RMVar_hsa_circ_332607,RMVar_hsa_circ_272859,RMVar_hsa_circ_324230,RMVar_hsa_circ_234589,RMVar_hsa_circ_338905,RMVar_hsa_circ_276121,RMVar_hsa_circ_234591 47050 RMVar_ID_47050 Human_SNP_ID_252319247 A-to-I Human chr5 + 134710398 134710398 134710398 CGATTATAGGCATGCACCACCACACCCCAGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCA CGATTATAGGCATGCACCACCACACCCCAGCTGATTTTTGTATTTTTAGTAGAGACAGGGTTTCA A G SEC24A Ensembl:ENSG00000113615 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs561983677 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123001,RMVar_hsa_circ_100845,RMVar_hsa_circ_234527,RMVar_hsa_circ_234528,RMVar_hsa_circ_115390,RMVar_hsa_circ_234529,RMVar_hsa_circ_105485,RMVar_hsa_circ_25480,RMVar_hsa_circ_79000,RMVar_hsa_circ_83820,RMVar_hsa_circ_24133,RMVar_hsa_circ_234543,RMVar_hsa_circ_234551,RMVar_hsa_circ_28635,RMVar_hsa_circ_41891,RMVar_hsa_circ_46528,RMVar_hsa_circ_39779,RMVar_hsa_circ_331870,RMVar_hsa_circ_286218,RMVar_hsa_circ_117210,RMVar_hsa_circ_234572,RMVar_hsa_circ_234573,RMVar_hsa_circ_360451,RMVar_hsa_circ_234575,RMVar_hsa_circ_353034,RMVar_hsa_circ_234574,RMVar_hsa_circ_342716,RMVar_hsa_circ_234587,RMVar_hsa_circ_120211,RMVar_hsa_circ_234581,RMVar_hsa_circ_355607,RMVar_hsa_circ_234585,RMVar_hsa_circ_51343,RMVar_hsa_circ_356437,RMVar_hsa_circ_284432,RMVar_hsa_circ_299082,RMVar_hsa_circ_234588,RMVar_hsa_circ_234592,RMVar_hsa_circ_295962,RMVar_hsa_circ_332607,RMVar_hsa_circ_272859,RMVar_hsa_circ_324230,RMVar_hsa_circ_234589,RMVar_hsa_circ_338905,RMVar_hsa_circ_276121,RMVar_hsa_circ_234591 47051 RMVar_ID_47051 Human_SNP_ID_252319521 A-to-I Human chr5 + 134711714 134711714 134711714 CACCACGCCTGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGG CACCACGCCTGGCTAATTTTTGTATTTTTAGTGGAGACGGGGTTTCACCATGTTGGCCAGGCTGG A G SEC24A Ensembl:ENSG00000113615 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs572952628 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123001,RMVar_hsa_circ_100845,RMVar_hsa_circ_234527,RMVar_hsa_circ_234528,RMVar_hsa_circ_115390,RMVar_hsa_circ_234529,RMVar_hsa_circ_105485,RMVar_hsa_circ_25480,RMVar_hsa_circ_79000,RMVar_hsa_circ_83820,RMVar_hsa_circ_24133,RMVar_hsa_circ_234543,RMVar_hsa_circ_234551,RMVar_hsa_circ_28635,RMVar_hsa_circ_41891,RMVar_hsa_circ_46528,RMVar_hsa_circ_39779,RMVar_hsa_circ_331870,RMVar_hsa_circ_286218,RMVar_hsa_circ_117210,RMVar_hsa_circ_234572,RMVar_hsa_circ_234573,RMVar_hsa_circ_360451,RMVar_hsa_circ_234575,RMVar_hsa_circ_353034,RMVar_hsa_circ_234574,RMVar_hsa_circ_342716,RMVar_hsa_circ_234587,RMVar_hsa_circ_120211,RMVar_hsa_circ_234581,RMVar_hsa_circ_355607,RMVar_hsa_circ_234585,RMVar_hsa_circ_51343,RMVar_hsa_circ_356437,RMVar_hsa_circ_284432,RMVar_hsa_circ_299082,RMVar_hsa_circ_234588,RMVar_hsa_circ_234592,RMVar_hsa_circ_295962,RMVar_hsa_circ_332607,RMVar_hsa_circ_272859,RMVar_hsa_circ_324230,RMVar_hsa_circ_234589,RMVar_hsa_circ_338905,RMVar_hsa_circ_276121,RMVar_hsa_circ_234591 47052 RMVar_ID_47052 Human_SNP_ID_252327213 A-to-I Human chr5 + 134742904 134742904 134742904 GGGACTACAGGCATGTGCCAACACGCACGGCTAATTTTTTGTATTTTTAGTAGAGATGGGGTTTC GGGACTACAGGCATGTGCCAACACGCACGGCTGATTTTTTGTATTTTTAGTAGAGATGGGGTTTC A G CAMLG Ensembl:ENSG00000164615 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1161634591 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_234596,RMVar_hsa_circ_270189 47053 RMVar_ID_47053 Human_SNP_ID_252327394 A-to-I Human chr5 + 134743704 134743704 134743704 ACTGGCCAACATGGTGAAACCCTGTCTCTACTAAAAATACAAAAATTAGCCAGGTGTGGTGGCGG ACTGGCCAACATGGTGAAACCCTGTCTCTACTGAAAATACAAAAATTAGCCAGGTGTGGTGGCGG A G CAMLG Ensembl:ENSG00000164615 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs756179860 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_234596,RMVar_hsa_circ_270189 47054 RMVar_ID_47054 Human_SNP_ID_252327596 A-to-I Human chr5 + 134744456 134744456 134744456 TGAGGCAGGAGAGTTGCTCCAACCCAGGAGGCAGAGGTTGCAGTGAGCCAAGATTGCGCCACTGC TGAGGCAGGAGAGTTGCTCCAACCCAGGAGGCGGAGGTTGCAGTGAGCCAAGATTGCGCCACTGC A G CAMLG Ensembl:ENSG00000164615 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1238977739 Functional Loss SNV dbSNP153 33..33 33 - - - 47055 RMVar_ID_47055 Human_SNP_ID_252328286 A-to-I Human chr5 + 134747035 134747035 134747035 GCTGACCCGGTGGCAGAGGTTTACAGTGAGCCAAGACAGCGCCACTGCACTCCAGCCTGGGCGAC GCTGACCCGGTGGCAGAGGTTTACAGTGAGCCGAGACAGCGCCACTGCACTCCAGCCTGGGCGAC A G CAMLG Ensembl:ENSG00000164615 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1260199975 Functional Loss SNV dbSNP153 33..33 33 - - - 47056 RMVar_ID_47056 Human_SNP_ID_252329052 A-to-I Human chr5 + 134750354 134750354 134750354 GAGATCAGGAGTTTGAGACCAGCCTGACCAACATGGTGAAATCCTGTCTCTACTAAAAATACAAA GAGATCAGGAGTTTGAGACCAGCCTGACCAACCTGGTGAAATCCTGTCTCTACTAAAAATACAAA A C CAMLG Ensembl:ENSG00000164615 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1196021317 Functional Loss SNV dbSNP153 33..33 33 - - - 47057 RMVar_ID_47057 Human_SNP_ID_252335120 A-to-I Human chr5 + 134772680 134772680 134772680 TGCATGCCACCACGCCCAGCTAATTTTTTGGTATTTTTCGTAGAAATGGGGTTTCCCCCTGTTGG TGCATGCCACCACGCCCAGCTAATTTTTTGGTGTTTTTCGTAGAAATGGGGTTTCCCCCTGTTGG A G DDX46 Ensembl:ENSG00000145833 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1419021782 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_367645 47058 RMVar_ID_47058 Human_SNP_ID_252336001 A-to-I Human chr5 + 134776269 134776269 134776269 AAAATTAGCTTGGTGTGGTGGCGCACACCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGAAGA AAAATTAGCTTGGTGTGGTGGCGCACACCTGTGGTCCCAGCTACTCGGGAGGCTGAGGCAGAAGA A G DDX46 Ensembl:ENSG00000145833 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs776704063 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55145,RMVar_hsa_circ_70760,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 47059 RMVar_ID_47059 Human_SNP_ID_252336558 A-to-I Human chr5 + 134778144 134778144 134778144 AGGCCTATGCAGTCTACCTACCTCAGCCTCCCAAGTAGCTGGAACTACATGTGTGCACCACCATG AGGCCTATGCAGTCTACCTACCTCAGCCTCCCGAGTAGCTGGAACTACATGTGTGCACCACCATG A G DDX46 Ensembl:ENSG00000145833 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1288560675 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8602916 RMVar_hsa_circ_55145,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_67576,RMVar_hsa_circ_309182,RMVar_hsa_circ_348128,RMVar_hsa_circ_351802,RMVar_hsa_circ_234598,RMVar_hsa_circ_361622,RMVar_hsa_circ_350703,RMVar_hsa_circ_334557,RMVar_hsa_circ_339485,RMVar_hsa_circ_317403,RMVar_hsa_circ_71038,RMVar_hsa_circ_75281,RMVar_hsa_circ_69003,RMVar_hsa_circ_234599,RMVar_hsa_circ_234600 47060 RMVar_ID_47060 Human_SNP_ID_252336563 A-to-I Human chr5 + 134778168 134778168 134778168 AGCCTCCCAAGTAGCTGGAACTACATGTGTGCACCACCATGCCTGGCTAATTTTTGTATTTTGGT AGCCTCCCAAGTAGCTGGAACTACATGTGTGCGCCACCATGCCTGGCTAATTTTTGTATTTTGGT A G DDX46 Ensembl:ENSG00000145833 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs375084854 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55145,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_67576,RMVar_hsa_circ_309182,RMVar_hsa_circ_348128,RMVar_hsa_circ_351802,RMVar_hsa_circ_234598,RMVar_hsa_circ_361622,RMVar_hsa_circ_350703,RMVar_hsa_circ_334557,RMVar_hsa_circ_339485,RMVar_hsa_circ_317403,RMVar_hsa_circ_71038,RMVar_hsa_circ_75281,RMVar_hsa_circ_69003,RMVar_hsa_circ_234599,RMVar_hsa_circ_234600 47061 RMVar_ID_47061 Human_SNP_ID_252336572 A-to-I Human chr5 + 134778215 134778215 134778215 TAATTTTTGTATTTTGGTAGAGATGAGGTTTTACCATGTTGCTCACGCTGGTCTCGAATTCCTGG TAATTTTTGTATTTTGGTAGAGATGAGGTTTTGCCATGTTGCTCACGCTGGTCTCGAATTCCTGG A G DDX46 Ensembl:ENSG00000145833 Protein coding intron GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line - 24183664,31158229 RNA-Seq:(High) rs1030440870 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15303339,Human_RBP_ID_24083555,Human_RBP_ID_25856099 RMVar_hsa_circ_55145,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_67576,RMVar_hsa_circ_309182,RMVar_hsa_circ_348128,RMVar_hsa_circ_351802,RMVar_hsa_circ_234598,RMVar_hsa_circ_361622,RMVar_hsa_circ_350703,RMVar_hsa_circ_334557,RMVar_hsa_circ_339485,RMVar_hsa_circ_317403,RMVar_hsa_circ_71038,RMVar_hsa_circ_75281,RMVar_hsa_circ_69003,RMVar_hsa_circ_234599,RMVar_hsa_circ_234600 47062 RMVar_ID_47062 Human_SNP_ID_252336585 A-to-I Human chr5 + 134778252 134778252 134778252 GTTGCTCACGCTGGTCTCGAATTCCTGGCCTCAAGTGAACCACCTGCCTCGGCCTCCCAAAATAC GTTGCTCACGCTGGTCTCGAATTCCTGGCCTCGAGTGAACCACCTGCCTCGGCCTCCCAAAATAC A G DDX46 Ensembl:ENSG00000145833 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1040369009 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15303344 RMVar_hsa_circ_55145,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_67576,RMVar_hsa_circ_309182,RMVar_hsa_circ_348128,RMVar_hsa_circ_351802,RMVar_hsa_circ_234598,RMVar_hsa_circ_361622,RMVar_hsa_circ_350703,RMVar_hsa_circ_334557,RMVar_hsa_circ_339485,RMVar_hsa_circ_317403,RMVar_hsa_circ_71038,RMVar_hsa_circ_75281,RMVar_hsa_circ_69003,RMVar_hsa_circ_234599,RMVar_hsa_circ_234600 47063 RMVar_ID_47063 Human_SNP_ID_252336591 A-to-I Human chr5 + 134778279 134778279 134778279 GCCTCAAGTGAACCACCTGCCTCGGCCTCCCAAAATACTTGGATTACAGGCATGAGCCACCATGC GCCTCAAGTGAACCACCTGCCTCGGCCTCCCAGAATACTTGGATTACAGGCATGAGCCACCATGC A G DDX46 Ensembl:ENSG00000145833 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs376545964 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23038713 RMVar_hsa_circ_55145,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_67576,RMVar_hsa_circ_309182,RMVar_hsa_circ_348128,RMVar_hsa_circ_351802,RMVar_hsa_circ_234598,RMVar_hsa_circ_361622,RMVar_hsa_circ_350703,RMVar_hsa_circ_334557,RMVar_hsa_circ_339485,RMVar_hsa_circ_317403,RMVar_hsa_circ_71038,RMVar_hsa_circ_75281,RMVar_hsa_circ_69003,RMVar_hsa_circ_234599,RMVar_hsa_circ_234600 47064 RMVar_ID_47064 Human_SNP_ID_252336592 A-to-I Human chr5 + 134778279 134778279 134778279 GCCTCAAGTGAACCACCTGCCTCGGCCTCCCAAAATACTTGGATTACAGGCATGAGCCACCATGC GCCTCAAGTGAACCACCTGCCTCGGCCTCCCATAATACTTGGATTACAGGCATGAGCCACCATGC A T DDX46 Ensembl:ENSG00000145833 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs376545964 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23038713 RMVar_hsa_circ_55145,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_67576,RMVar_hsa_circ_309182,RMVar_hsa_circ_348128,RMVar_hsa_circ_351802,RMVar_hsa_circ_234598,RMVar_hsa_circ_361622,RMVar_hsa_circ_350703,RMVar_hsa_circ_334557,RMVar_hsa_circ_339485,RMVar_hsa_circ_317403,RMVar_hsa_circ_71038,RMVar_hsa_circ_75281,RMVar_hsa_circ_69003,RMVar_hsa_circ_234599,RMVar_hsa_circ_234600 47065 RMVar_ID_47065 Human_SNP_ID_252336877 A-to-I Human chr5 + 134779306 134779306 134779306 CCCTGTGCCTCCCAGGCTCAAGTGATTCTCCTACCTCAGCCTCCCGAGTAGCTGGGATTACAGGC CCCTGTGCCTCCCAGGCTCAAGTGATTCTCCTTCCTCAGCCTCCCGAGTAGCTGGGATTACAGGC A T DDX46 Ensembl:ENSG00000145833 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1268578300 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55145,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_67576,RMVar_hsa_circ_309182,RMVar_hsa_circ_348128,RMVar_hsa_circ_351802,RMVar_hsa_circ_234598,RMVar_hsa_circ_361622,RMVar_hsa_circ_350703,RMVar_hsa_circ_334557,RMVar_hsa_circ_339485,RMVar_hsa_circ_317403,RMVar_hsa_circ_71038,RMVar_hsa_circ_75281,RMVar_hsa_circ_69003,RMVar_hsa_circ_234599,RMVar_hsa_circ_234600 47066 RMVar_ID_47066 Human_SNP_ID_252336922 A-to-I Human chr5 + 134779468 134779468 134779468 TGTCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAAGCGTGAGCCACCACACTCGGCCTTATTTT TGTCTGCCTTGGCCTCCCAAAGTGCTGGGATTTCAAGCGTGAGCCACCACACTCGGCCTTATTTT A T DDX46 Ensembl:ENSG00000145833 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968401690 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55145,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_67576,RMVar_hsa_circ_309182,RMVar_hsa_circ_348128,RMVar_hsa_circ_351802,RMVar_hsa_circ_234598,RMVar_hsa_circ_361622,RMVar_hsa_circ_350703,RMVar_hsa_circ_334557,RMVar_hsa_circ_339485,RMVar_hsa_circ_317403,RMVar_hsa_circ_71038,RMVar_hsa_circ_75281,RMVar_hsa_circ_69003,RMVar_hsa_circ_234599,RMVar_hsa_circ_234600 47067 RMVar_ID_47067 Human_SNP_ID_252337039 A-to-I Human chr5 + 134779889 134779889 134779889 GGGAGGCCGAGGCAGACGGATCACCTGAGGTCAGGAGTTAGAGATCAGCCTGGCCAACATGGCAA GGGAGGCCGAGGCAGACGGATCACCTGAGGTCTGGAGTTAGAGATCAGCCTGGCCAACATGGCAA A T DDX46 Ensembl:ENSG00000145833 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1459647488 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55145,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_67576,RMVar_hsa_circ_309182,RMVar_hsa_circ_348128,RMVar_hsa_circ_351802,RMVar_hsa_circ_234598,RMVar_hsa_circ_361622,RMVar_hsa_circ_350703,RMVar_hsa_circ_334557,RMVar_hsa_circ_339485,RMVar_hsa_circ_317403,RMVar_hsa_circ_71038,RMVar_hsa_circ_75281,RMVar_hsa_circ_69003,RMVar_hsa_circ_234599,RMVar_hsa_circ_234600 47068 RMVar_ID_47068 Human_SNP_ID_252337403 A-to-I Human chr5 + 134780828 134780828 134780828 GAGGCTGGTGGATCACTGGAGCCAAGTAGTTCAAGACCAGCCTGGGCAACATAGCATGACTCTTT GAGGCTGGTGGATCACTGGAGCCAAGTAGTTCGAGACCAGCCTGGGCAACATAGCATGACTCTTT A G DDX46 Ensembl:ENSG00000145833 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs1192574439 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15303431,Human_RBP_ID_25936645 RMVar_hsa_circ_55145,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_67576,RMVar_hsa_circ_309182,RMVar_hsa_circ_348128,RMVar_hsa_circ_351802,RMVar_hsa_circ_234598,RMVar_hsa_circ_361622,RMVar_hsa_circ_350703,RMVar_hsa_circ_334557,RMVar_hsa_circ_339485,RMVar_hsa_circ_317403,RMVar_hsa_circ_71038,RMVar_hsa_circ_75281,RMVar_hsa_circ_69003,RMVar_hsa_circ_234599,RMVar_hsa_circ_234600 47069 RMVar_ID_47069 Human_SNP_ID_252337409 A-to-I Human chr5 + 134780848 134780848 134780848 GCCAAGTAGTTCAAGACCAGCCTGGGCAACATAGCATGACTCTTTCTACTAAAAAACAAAAAAAA GCCAAGTAGTTCAAGACCAGCCTGGGCAACATGGCATGACTCTTTCTACTAAAAAACAAAAAAAA A G DDX46 Ensembl:ENSG00000145833 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs1242261863 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15303435 RMVar_hsa_circ_55145,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_67576,RMVar_hsa_circ_309182,RMVar_hsa_circ_348128,RMVar_hsa_circ_351802,RMVar_hsa_circ_234598,RMVar_hsa_circ_361622,RMVar_hsa_circ_350703,RMVar_hsa_circ_334557,RMVar_hsa_circ_339485,RMVar_hsa_circ_317403,RMVar_hsa_circ_71038,RMVar_hsa_circ_75281,RMVar_hsa_circ_69003,RMVar_hsa_circ_234599,RMVar_hsa_circ_234600 47070 RMVar_ID_47070 Human_SNP_ID_252349945 A-to-I Human chr5 + 134829698 134829698 134829698 TTGTGTTTTTGAGGCTGGGCGCAGTGACTCACACCTGTATCCCAGCAATTTGGGAGGCCGAGGTG TTGTGTTTTTGAGGCTGGGCGCAGTGACTCACGCCTGTATCCCAGCAATTTGGGAGGCCGAGGTG A G DDX46 Ensembl:ENSG00000145833 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1364137670 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_788012,Human_RBP_ID_7385806 RMVar_hsa_circ_234601,RMVar_hsa_circ_266438,RMVar_hsa_circ_117773,RMVar_hsa_circ_234622 47071 RMVar_ID_47071 Human_SNP_ID_252354648 A-to-I Human chr5 + 134847754 134847754 134847754 CCTGAGATGGAGTCTGTTTCCTAGGCTGGAGTACAGTGGCACGAACTCGGCTCACTGCAACCTCC CCTGAGATGGAGTCTGTTTCCTAGGCTGGAGTGCAGTGGCACGAACTCGGCTCACTGCAACCTCC A G DDX46,C5orf24 Ensembl:ENSG00000145833,Ensembl:ENSG00000181904 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1486490398 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15305026,Human_RBP_ID_17575899,Human_RBP_ID_22482025 RMVar_hsa_circ_107835,RMVar_hsa_circ_110532,RMVar_hsa_circ_234623,RMVar_hsa_circ_234624 47072 RMVar_ID_47072 Human_SNP_ID_252354680 A-to-I Human chr5 + 134847865 134847865 134847865 GGAGTTACAGGCACCCGCCACCATGCCTGACTAATTTTTTGGATTTTTAGAGAGAGGGTTTCGCT GGAGTTACAGGCACCCGCCACCATGCCTGACTGATTTTTTGGATTTTTAGAGAGAGGGTTTCGCT A G DDX46,C5orf24 Ensembl:ENSG00000145833,Ensembl:ENSG00000181904 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs116564931 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17575486 RMVar_hsa_circ_107835,RMVar_hsa_circ_110532,RMVar_hsa_circ_234623,RMVar_hsa_circ_234624 47073 RMVar_ID_47073 Human_SNP_ID_252355120 A-to-I Human chr5 + 134849174 134849174 134849174 CTACTTCGGAGGCTGAGGCAGGAGAATCGCTTAAACCGGGGTTCCAGAGGTTGCAGTGAGCCAAG CTACTTCGGAGGCTGAGGCAGGAGAATCGCTTCAACCGGGGTTCCAGAGGTTGCAGTGAGCCAAG A C DDX46,C5orf24 Ensembl:ENSG00000145833,Ensembl:ENSG00000181904 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs958749963 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7385946 RMVar_hsa_circ_107835,RMVar_hsa_circ_110532,RMVar_hsa_circ_234623,RMVar_hsa_circ_234624 47074 RMVar_ID_47074 Human_SNP_ID_252355127 A-to-I Human chr5 + 134849204 134849204 134849204 TTAAACCGGGGTTCCAGAGGTTGCAGTGAGCCAAGATCAAGTCACTGCACTCCAGCCTGGGCAAC TTAAACCGGGGTTCCAGAGGTTGCAGTGAGCCGAGATCAAGTCACTGCACTCCAGCCTGGGCAAC A G DDX46,C5orf24 Ensembl:ENSG00000145833,Ensembl:ENSG00000181904 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs977619259 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15305058,Human_RBP_ID_25856970 RMVar_hsa_circ_107835,RMVar_hsa_circ_110532,RMVar_hsa_circ_234623,RMVar_hsa_circ_234624 47075 RMVar_ID_47075 Human_SNP_ID_252355345 A-to-I Human chr5 + 134849832 134849824 134849833 AGTGCATGCCTCCATGCCCAGCTAATTTTTGTATTTTTTGTAGTGACGGGGTTTCTCCCTGTTGG AGTGCATGCCTCCATGCCCAGCTAA_________TTTTTGTAGTGACGGGGTTTCTCCCTGTTGG ATTTTTGTAT A DDX46,C5orf24 Ensembl:ENSG00000145833,Ensembl:ENSG00000181904 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1217829493 Functional Loss DEL dbSNP153 26..34 33 - - - RMVar_hsa_circ_107835,RMVar_hsa_circ_110532,RMVar_hsa_circ_234623,RMVar_hsa_circ_234624 47076 RMVar_ID_47076 Human_SNP_ID_252355565 A-to-I Human chr5 + 134850612 134850612 134850612 CTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCGTGCACCACTACACCAGGCTAATTTTT CTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTGCAGGCGTGCACCACTACACCAGGCTAATTTTT A G DDX46,C5orf24 Ensembl:ENSG00000145833,Ensembl:ENSG00000181904 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1401885539 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107835,RMVar_hsa_circ_110532,RMVar_hsa_circ_234623,RMVar_hsa_circ_234624 47077 RMVar_ID_47077 Human_SNP_ID_252355795 A-to-I Human chr5 + 134851128 134851128 134851128 TTTTGTATTTTTAGTAGAAACAGGGTTTTGCCATTTTGGCCAAGCTGGTCTTGAACTCCTGACCT TTTTGTATTTTTAGTAGAAACAGGGTTTTGCCGTTTTGGCCAAGCTGGTCTTGAACTCCTGACCT A G DDX46,C5orf24 Ensembl:ENSG00000145833,Ensembl:ENSG00000181904 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs995839955 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107835,RMVar_hsa_circ_110532,RMVar_hsa_circ_234623,RMVar_hsa_circ_234624 47078 RMVar_ID_47078 Human_SNP_ID_252356575 A-to-I Human chr5 + 134854005 134854005 134854005 AGGAGGCTGAGGCAGGAGAATCACTTGAACCCAGGAGGCGGAAGTTGCAGTGAGCTGAGATCGAG AGGAGGCTGAGGCAGGAGAATCACTTGAACCCTGGAGGCGGAAGTTGCAGTGAGCTGAGATCGAG A T DDX46,C5orf24 Ensembl:ENSG00000145833,Ensembl:ENSG00000181904 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1426993258 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107835,RMVar_hsa_circ_110532,RMVar_hsa_circ_234623,RMVar_hsa_circ_234624 47079 RMVar_ID_47079 Human_SNP_ID_252368272 A-to-I Human chr5 + 134900401 134900401 134900401 GAACCTTAAAATGTTCCCAGCAGGCTGGGCGCAGTGGCTCATGCCTGTAATCCCAGCACTTTGGG GAACCTTAAAATGTTCCCAGCAGGCTGGGCGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGG A G TXNDC15 Ensembl:ENSG00000113621 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1014341279 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8214090 Human_miRNA_ID_1360135 47080 RMVar_ID_47080 Human_SNP_ID_252368282 A-to-I Human chr5 + 134900439 134900439 134900439 TCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGAGGATCACTTGAGGTTAGGACTTTT TCATGCCTGTAATCCCAGCACTTTGGGAGGCCTAGGCGGGAGGATCACTTGAGGTTAGGACTTTT A T TXNDC15 Ensembl:ENSG00000113621 Protein coding 3'UTR GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 29129909,30559470 RNA-Seq:(High) rs1291611822 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15306069 47081 RMVar_ID_47081 Human_SNP_ID_252368304 A-to-I Human chr5 + 134900509 134900509 134900509 CAGCCTGGCCAACTTGGTGAAACCCTCTCTCTACTAAAAATACAAAAAATTAGCTGGGCGTGGTG CAGCCTGGCCAACTTGGTGAAACCCTCTCTCTGCTAAAAATACAAAAAATTAGCTGGGCGTGGTG A G TXNDC15 Ensembl:ENSG00000113621 Protein coding 3'UTR GSE47997;GSE38233;GSE99789 K562 cells&HepG2 cells;cultured B-cells;esophageal squamous carcinoma cells,EC109 - 23474544,24183664,29796672 RNA-Seq:(High) rs959243835 Functional Loss SNV dbSNP153 33..33 33 - - - 47082 RMVar_ID_47082 Human_SNP_ID_252368305 A-to-I Human chr5 + 134900512 134900512 134900512 CCTGGCCAACTTGGTGAAACCCTCTCTCTACTAAAAATACAAAAAATTAGCTGGGCGTGGTGGCG CCTGGCCAACTTGGTGAAACCCTCTCTCTACTGAAAATACAAAAAATTAGCTGGGCGTGGTGGCG A G TXNDC15 Ensembl:ENSG00000113621 Protein coding 3'UTR GSE47997;GSE38233;GSE99789 K562 cells&HepG2 cells;cultured B-cells;esophageal squamous carcinoma cells,EC109 - 23474544,24183664,29796672 RNA-Seq:(High) rs145434259 Functional Loss SNV dbSNP153 33..33 33 - - - 47083 RMVar_ID_47083 Human_SNP_ID_252368327 A-to-I Human chr5 + 134900591 134900591 134900591 CAGCTACTTGGGAAAGCTGAGGCATGAGAATCACTTGAACCCGGGAGGCAGAGGTTGCAGTGAGC CAGCTACTTGGGAAAGCTGAGGCATGAGAATCGCTTGAACCCGGGAGGCAGAGGTTGCAGTGAGC A G TXNDC15 Ensembl:ENSG00000113621 Protein coding 3'UTR GSE100210;GSE99789;GSE107867;GSE107867 HepG2 cell line;esophageal squamous carcinoma cells,EC109;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;ASD brains,temporal_cortex - 29129909,29796672,30559470,30559470 RNA-Seq:(High) rs909640297 Functional Loss SNV dbSNP153 33..33 33 - - - 47084 RMVar_ID_47084 Human_SNP_ID_252368369 A-to-I Human chr5 + 134900807 134900807 134900807 ATGTAATTTAAACAAACTTTTTTTTTTTTTTTAGACAAAGTCTCACTCTGTCACCTAGGCTGGAG ATGTAATTTAAACAAACTTTTTTTTTTTTTTTTGACAAAGTCTCACTCTGTCACCTAGGCTGGAG A T TXNDC15 Ensembl:ENSG00000113621 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1273200595 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7386279 47085 RMVar_ID_47085 Human_SNP_ID_252368376 A-to-I Human chr5 + 134900819 134900815 134900819 CAAACTTTTTTTTTTTTTTTAGACAAAGTCTCACTCTGTCACCTAGGCTGGAGTGCAATGGTGCA CAAACTTTTTTTTTTTTTTTAGACAAAGT____CTCTGTCACCTAGGCTGGAGTGCAATGGTGCA TCTCA T TXNDC15 Ensembl:ENSG00000113621 Protein coding 3'UTR GSE38233;GSE100210;GSE107867;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,cerebellum;ASD brains,temporal_cortex - 24183664,29129909,30559470,30559470 RNA-Seq:(High) rs568722829 Functional Loss DEL dbSNP153 30..33 33 - - - 47086 RMVar_ID_47086 Human_SNP_ID_252368379 A-to-I Human chr5 + 134900843 134900843 134900843 AAAGTCTCACTCTGTCACCTAGGCTGGAGTGCAATGGTGCAATCTTGGCTCACTGCAACCTCTGC AAAGTCTCACTCTGTCACCTAGGCTGGAGTGCCATGGTGCAATCTTGGCTCACTGCAACCTCTGC A C TXNDC15 Ensembl:ENSG00000113621 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1031786351 Functional Loss SNV dbSNP153 33..33 33 - - - 47087 RMVar_ID_47087 Human_SNP_ID_252368396 A-to-I Human chr5 + 134900917 134900917 134900917 TCAAGCGATTCTCCAGCCTCAGCCTCCTGAGTAGCTGGGACTATGGGCCTGTGCCATCACACCCA TCAAGCGATTCTCCAGCCTCAGCCTCCTGAGTGGCTGGGACTATGGGCCTGTGCCATCACACCCA A G TXNDC15 Ensembl:ENSG00000113621 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1401254586 Functional Loss SNV dbSNP153 33..33 33 - - - 47088 RMVar_ID_47088 Human_SNP_ID_252368403 A-to-I Human chr5 + 134900953 134900953 134900953 GGGACTATGGGCCTGTGCCATCACACCCAGCTAATTTTTCTATTTTTAGTAGAGATGGGGTTTTG GGGACTATGGGCCTGTGCCATCACACCCAGCTTATTTTTCTATTTTTAGTAGAGATGGGGTTTTG A T TXNDC15 Ensembl:ENSG00000113621 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1029607184 Functional Loss SNV dbSNP153 33..33 33 - - - 47089 RMVar_ID_47089 Human_SNP_ID_252368408 A-to-I Human chr5 + 134900971 134900967 134900972 CATCACACCCAGCTAATTTTTCTATTTTTAGTAGAGATGGGGTTTTGCCATGTTGGCCAGGCTGG CATCACACCCAGCTAATTTTTCTATTTTT_____AGATGGGGTTTTGCCATGTTGGCCAGGCTGG TAGTAG T TXNDC15 Ensembl:ENSG00000113621 Protein coding 3'UTR GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 29129909,30559470 RNA-Seq:(High) rs983033859 Functional Loss DEL dbSNP153 30..34 33 - - - 47090 RMVar_ID_47090 Human_SNP_ID_252368409 A-to-I Human chr5 + 134900968 134900968 134900968 TGCCATCACACCCAGCTAATTTTTCTATTTTTAGTAGAGATGGGGTTTTGCCATGTTGGCCAGGC TGCCATCACACCCAGCTAATTTTTCTATTTTTGGTAGAGATGGGGTTTTGCCATGTTGGCCAGGC A G TXNDC15 Ensembl:ENSG00000113621 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1410751974 Functional Loss SNV dbSNP153 33..33 33 - - - 47091 RMVar_ID_47091 Human_SNP_ID_252368422 A-to-I Human chr5 + 134901040 134901040 134901040 AAACTGCTGACTTCAGGTGATCCACCCGCCTCAGCCTCCCAAAGTGTTGGGATTACAGGTGTGAG AAACTGCTGACTTCAGGTGATCCACCCGCCTCCGCCTCCCAAAGTGTTGGGATTACAGGTGTGAG A C TXNDC15 Ensembl:ENSG00000113621 Protein coding 3'UTR GSE47997;GSE126723:GSM3611827,GSM3611828,GSM3611829 K562 cells&HepG2 cells;Bronchiolar epithelium,BEP2D cell line - 23474544,31158229 RNA-Seq:(High) rs908358564 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_289699 47092 RMVar_ID_47092 Human_SNP_ID_252368425 A-to-I Human chr5 + 134901049 134901049 134901049 ACTTCAGGTGATCCACCCGCCTCAGCCTCCCAAAGTGTTGGGATTACAGGTGTGAGCCACTGCGC ACTTCAGGTGATCCACCCGCCTCAGCCTCCCAGAGTGTTGGGATTACAGGTGTGAGCCACTGCGC A G TXNDC15 Ensembl:ENSG00000113621 Protein coding 3'UTR GSE47997;GSE126723:GSM3611827,GSM3611828,GSM3611829 K562 cells&HepG2 cells;Bronchiolar epithelium,BEP2D cell line - 23474544,31158229 RNA-Seq:(High) rs909596961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_289699 47093 RMVar_ID_47093 Human_SNP_ID_252368597 A-to-I Human chr5 + 134901743 134901742 134901743 GCTGGTTAACATGGCGAAACCCTGTCTTTACTAAAAGTACAAAAAATTAGCTGGGTGTGGTGGTG GCTGGTTAACATGGCGAAACCCTGTCTTTACT_AAAGTACAAAAAATTAGCTGGGTGTGGTGGTG TA T RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1462416877 Functional Loss DEL dbSNP153 33..33 33 - - - 47094 RMVar_ID_47094 Human_SNP_ID_252370283 A-to-I Human chr5 + 134907324 134907324 134907324 TGGAGTGCAGTGGTGCGGTCTTGGCGCACTGCAACTTTGCCTCCTGGGTTCAAGCGATTCTCCTG TGGAGTGCAGTGGTGCGGTCTTGGCGCACTGCGACTTTGCCTCCTGGGTTCAAGCGATTCTCCTG A G PCBD2 Ensembl:ENSG00000132570 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1003907660 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_234628,RMVar_hsa_circ_76520 47095 RMVar_ID_47095 Human_SNP_ID_252370499 A-to-I Human chr5 + 134908049 134908049 134908049 TCAAGTGATCCTCCCACCTCAGCCTCCCAAGTAGCTGAGACTATGGACATGGTCCACCACACCCG TCAAGTGATCCTCCCACCTCAGCCTCCCAAGTCGCTGAGACTATGGACATGGTCCACCACACCCG A C PCBD2 Ensembl:ENSG00000132570 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251628510 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15306163 RMVar_hsa_circ_234628,RMVar_hsa_circ_76520 47096 RMVar_ID_47096 Human_SNP_ID_252370538 A-to-I Human chr5 + 134908190 134908190 134908190 ATGATCCTCCCACCTCAGCTTCCCAAAGTGCCAGGATTACAGATGTGAGCCACTGTGCCCAGCCC ATGATCCTCCCACCTCAGCTTCCCAAAGTGCCGGGATTACAGATGTGAGCCACTGTGCCCAGCCC A G PCBD2 Ensembl:ENSG00000132570 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs549583677 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_234628,RMVar_hsa_circ_76520 47097 RMVar_ID_47097 Human_SNP_ID_252371000 A-to-I Human chr5 + 134910125 134910125 134910125 AGAAGCTGAATTGTGAAGTTTGAGGCAGCAGTAAGGGAGCCAGAGGTGACATGCCATGGAGGCAG AGAAGCTGAATTGTGAAGTTTGAGGCAGCAGTGAGGGAGCCAGAGGTGACATGCCATGGAGGCAG A G PCBD2 Ensembl:ENSG00000132570 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904445405 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_234628,RMVar_hsa_circ_76520 47098 RMVar_ID_47098 Human_SNP_ID_252372412 A-to-I Human chr5 + 134916143 134916143 134916143 AGACTCCATCTCTACAAAAATAAAAATTAGCCAAGAGTGGTGGCATGCACCTGTGGTCTCAGTTA AGACTCCATCTCTACAAAAATAAAAATTAGCCGAGAGTGGTGGCATGCACCTGTGGTCTCAGTTA A G PCBD2 Ensembl:ENSG00000132570 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1265826640 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 47099 RMVar_ID_47099 Human_SNP_ID_252375655 A-to-I Human chr5 - 134927780 134927779 134927780 CACAATCATGGCAAGCCAACGCCACTTATCCAATGAACCACTATCACGAAAAAAACTCTACCTCT CACAATCATGGCAAGCCAACGCCACTTATCCA_TGAACCACTATCACGAAAAAAACTCTACCTCT AT A MTND4P12 Ensembl:ENSG00000247627 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1554165834 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_3784706,Human_RBP_ID_4847332,Human_RBP_ID_5214838,Human_RBP_ID_5641143,Human_RBP_ID_8894364,Human_RBP_ID_9341537,Human_RBP_ID_9437212,Human_RBP_ID_10232000,Human_RBP_ID_17090681,Human_RBP_ID_17196269,Human_RBP_ID_17209363,Human_RBP_ID_17416415,Human_RBP_ID_17584740,Human_RBP_ID_18170750,Human_RBP_ID_18538373,Human_RBP_ID_18544890,Human_RBP_ID_18927262,Human_RBP_ID_18956906,Human_RBP_ID_21120179,Human_RBP_ID_21945207,Human_RBP_ID_21990527,Human_RBP_ID_26521472 Human_miRNA_ID_1827577 47100 RMVar_ID_47100 Human_SNP_ID_252375656 A-to-I Human chr5 - 134927780 134927780 134927780 CACAATCATGGCAAGCCAACGCCACTTATCCAATGAACCACTATCACGAAAAAAACTCTACCTCT CACAATCATGGCAAGCCAACGCCACTTATCCAGTGAACCACTATCACGAAAAAAACTCTACCTCT T C MTND4P12 Ensembl:ENSG00000247627 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs12332606 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3784706,Human_RBP_ID_4847332,Human_RBP_ID_5214838,Human_RBP_ID_5641143,Human_RBP_ID_8894364,Human_RBP_ID_9341537,Human_RBP_ID_9437212,Human_RBP_ID_10232000,Human_RBP_ID_17090681,Human_RBP_ID_17196269,Human_RBP_ID_17209363,Human_RBP_ID_17416415,Human_RBP_ID_17584740,Human_RBP_ID_18170750,Human_RBP_ID_18538373,Human_RBP_ID_18544890,Human_RBP_ID_18927262,Human_RBP_ID_18956906,Human_RBP_ID_21120179,Human_RBP_ID_21945207,Human_RBP_ID_21990527,Human_RBP_ID_26521472 Human_miRNA_ID_1827577 47101 RMVar_ID_47101 Human_SNP_ID_252375660 A-to-I Human chr5 - 134927794 134927794 134927794 TGACTCCTGCCCCTCACAATCATGGCAAGCCAACGCCACTTATCCAATGAACCACTATCACGAAA TGACTCCTGCCCCTCACAATCATGGCAAGCCAGCGCCACTTATCCAATGAACCACTATCACGAAA T C MTND4P12 Ensembl:ENSG00000247627 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs748113131 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8894364,Human_RBP_ID_17090681,Human_RBP_ID_17196271,Human_RBP_ID_18538373,Human_RBP_ID_18927262,Human_RBP_ID_18956906,Human_RBP_ID_21945207 47102 RMVar_ID_47102 Human_SNP_ID_252375958 A-to-I Human chr5 + 134928779 134928779 134928779 ATGGTGTAAACCCGGGAGGCAGAGCTTGCAGTAAGCCAAGATCGTGCCACTCCAGCCTAGGCAAC ATGGTGTAAACCCGGGAGGCAGAGCTTGCAGTGAGCCAAGATCGTGCCACTCCAGCCTAGGCAAC A G PCBD2 Ensembl:ENSG00000132570 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1028963995 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 47103 RMVar_ID_47103 Human_SNP_ID_252382986 A-to-I Human chr5 + 134960828 134960828 134960828 TTGCTCTGTCGCCCAGGCCAGAGTGCAGTGGTATGATCTCGGCTCACTGTAACCTCCGCCTCCCA TTGCTCTGTCGCCCAGGCCAGAGTGCAGTGGTGTGATCTCGGCTCACTGTAACCTCCGCCTCCCA A G PCBD2 Ensembl:ENSG00000132570 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs367972464 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_31994,RMVar_hsa_circ_234628,RMVar_hsa_circ_76520,RMVar_hsa_circ_119817,RMVar_hsa_circ_324049,RMVar_hsa_circ_234629,RMVar_hsa_circ_55150 47104 RMVar_ID_47104 Human_SNP_ID_252383229 A-to-I Human chr5 + 134961861 134961861 134961861 ACGGTTTATTGCAGCCTTAACCTCCTGGGCTCAAGCAGTTCTCCCTCCTCAGCCTCCAGAGTAGC ACGGTTTATTGCAGCCTTAACCTCCTGGGCTCTAGCAGTTCTCCCTCCTCAGCCTCCAGAGTAGC A T PCBD2 Ensembl:ENSG00000132570 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs561734762 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_31994,RMVar_hsa_circ_234628,RMVar_hsa_circ_76520,RMVar_hsa_circ_119817,RMVar_hsa_circ_324049,RMVar_hsa_circ_234629,RMVar_hsa_circ_55150 47105 RMVar_ID_47105 Human_SNP_ID_252384365 A-to-I Human chr5 + 134966743 134966743 134966743 TTTTTTTTTTTTAAGAGATGGGGTCTCATTCTATCATGCAGACTGGAGTGCAGTGGTGTGATCAC TTTTTTTTTTTTAAGAGATGGGGTCTCATTCTGTCATGCAGACTGGAGTGCAGTGGTGTGATCAC A G PCBD2 Ensembl:ENSG00000132570 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs546378245 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_31994,RMVar_hsa_circ_324049,RMVar_hsa_circ_55150 47106 RMVar_ID_47106 Human_SNP_ID_252384366 A-to-I Human chr5 + 134966743 134966743 134966743 TTTTTTTTTTTTAAGAGATGGGGTCTCATTCTATCATGCAGACTGGAGTGCAGTGGTGTGATCAC TTTTTTTTTTTTAAGAGATGGGGTCTCATTCTTTCATGCAGACTGGAGTGCAGTGGTGTGATCAC A T PCBD2 Ensembl:ENSG00000132570 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs546378245 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_31994,RMVar_hsa_circ_324049,RMVar_hsa_circ_55150 47107 RMVar_ID_47107 Human_SNP_ID_252384831 A-to-I Human chr5 + 134968580 134968580 134968580 CGGAGTGATGGTGTGCACCTGTTGTCCCAGCTACTCAGGATGCTGAGGCAGGAGAATCCCTTTAA CGGAGTGATGGTGTGCACCTGTTGTCCCAGCTGCTCAGGATGCTGAGGCAGGAGAATCCCTTTAA A G CATSPER3,PCBD2 Ensembl:ENSG00000152705,Ensembl:ENSG00000132570 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991027464 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_31994,RMVar_hsa_circ_324049,RMVar_hsa_circ_55150 47108 RMVar_ID_47108 Human_SNP_ID_406707632 A-to-I Human chr9 - 91292416 91292416 91292416 GAATTAGCCAGTCATGGTGGTGCGTGCTTGTAATCACAGCTACCTGGGAGGCTGAGGCAGGAGAA GAATTAGCCAGTCATGGTGGTGCGTGCTTGTAGTCACAGCTACCTGGGAGGCTGAGGCAGGAGAA T C AUH Ensembl:ENSG00000148090 Protein coding intron GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs1245745721 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_257732,RMVar_hsa_circ_257733,RMVar_hsa_circ_257734 47109 RMVar_ID_47109 Human_SNP_ID_406707633 A-to-I Human chr9 - 91292417 91292417 91292417 AGAATTAGCCAGTCATGGTGGTGCGTGCTTGTAATCACAGCTACCTGGGAGGCTGAGGCAGGAGA AGAATTAGCCAGTCATGGTGGTGCGTGCTTGTTATCACAGCTACCTGGGAGGCTGAGGCAGGAGA T A AUH Ensembl:ENSG00000148090 Protein coding intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1446076932 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_257732,RMVar_hsa_circ_257733,RMVar_hsa_circ_257734 47110 RMVar_ID_47110 Human_SNP_ID_406707640 A-to-I Human chr9 - 91292439 91292439 91292439 CCCCGTCTCTACTAAAAATAGAAGAATTAGCCAGTCATGGTGGTGCGTGCTTGTAATCACAGCTA CCCCGTCTCTACTAAAAATAGAAGAATTAGCCGGTCATGGTGGTGCGTGCTTGTAATCACAGCTA T C AUH Ensembl:ENSG00000148090 Protein coding intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1372738962 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_257732,RMVar_hsa_circ_257733,RMVar_hsa_circ_257734 47111 RMVar_ID_47111 Human_SNP_ID_406708078 A-to-I Human chr9 - 91294315 91294315 91294315 TTGATCTCTTGACCTCATGATCTGCCTGCCTCAAGCTCCCAAAGTGCTGGGATTACAGGCGTGAG TTGATCTCTTGACCTCATGATCTGCCTGCCTCCAGCTCCCAAAGTGCTGGGATTACAGGCGTGAG T G AUH Ensembl:ENSG00000148090 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1372194569 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_257732,RMVar_hsa_circ_257733,RMVar_hsa_circ_257734 47112 RMVar_ID_47112 Human_SNP_ID_406708096 A-to-I Human chr9 - 91294382 91294374 91294383 CACCGTGCCCAGCTAATTTTTGTATTTTTTGTAGAGACGGAGTTTCACCATGTTGGCCAGGATGG CACCGTGCCCAGCTAATTTTTGTATTTTTTG_________AGTTTCACCATGTTGGCCAGGATGG TCCGTCTCTA T AUH Ensembl:ENSG00000148090 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947356960 Functional Loss DEL dbSNP153 32..40 33 - - - RMVar_hsa_circ_257735,RMVar_hsa_circ_257732,RMVar_hsa_circ_257733,RMVar_hsa_circ_257734,RMVar_hsa_circ_122155 47113 RMVar_ID_47113 Human_SNP_ID_406720225 A-to-I Human chr9 - 91346298 91346298 91346298 GGCCTCTTTACATAATGATTGATTACATCATTAGCCATTGGCGACTGAGCTCAATCTCCAGCTCC GGCCTCTTTACATAATGATTGATTACATCATTTGCCATTGGCGACTGAGCTCAATCTCCAGCTCC T A AUH Ensembl:ENSG00000148090 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1436827211 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104144,RMVar_hsa_circ_257735,RMVar_hsa_circ_257734,RMVar_hsa_circ_122155,RMVar_hsa_circ_307522,RMVar_hsa_circ_363939,RMVar_hsa_circ_257736,RMVar_hsa_circ_257737,RMVar_hsa_circ_257744,RMVar_hsa_circ_65323,RMVar_hsa_circ_338422,RMVar_hsa_circ_282570,RMVar_hsa_circ_31985,RMVar_hsa_circ_257743 47114 RMVar_ID_47114 Human_SNP_ID_406722437 A-to-I Human chr9 - 91355435 91355435 91355435 CTCCCGCCTCAGCCCCCCGAGTAGCTGGGATTACAGGCGCCTGCCACCTCGCCTAGCTAATTTTT CTCCCGCCTCAGCCCCCCGAGTAGCTGGGATTGCAGGCGCCTGCCACCTCGCCTAGCTAATTTTT T C AUH Ensembl:ENSG00000148090 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs577825700 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104144,RMVar_hsa_circ_257735,RMVar_hsa_circ_257734,RMVar_hsa_circ_122155,RMVar_hsa_circ_307522,RMVar_hsa_circ_363939,RMVar_hsa_circ_257736,RMVar_hsa_circ_257737,RMVar_hsa_circ_257744,RMVar_hsa_circ_65323,RMVar_hsa_circ_338422,RMVar_hsa_circ_282570,RMVar_hsa_circ_31985,RMVar_hsa_circ_257743 47115 RMVar_ID_47115 Human_SNP_ID_406854466 A-to-I Human chr9 - 91896524 91896524 91896524 TGATGTGAGCAGGCACTTTTGAGGTATAAGAAACTGTCAAGTGATTATTCACACTTCTGTTGGCT TGATGTGAGCAGGCACTTTTGAGGTATAAGAAGCTGTCAAGTGATTATTCACACTTCTGTTGGCT T C ROR2 Ensembl:ENSG00000169071 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1266620163 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_322347 47116 RMVar_ID_47116 Human_SNP_ID_406854467 A-to-I Human chr9 - 91896529 91896529 91896529 CATGCTGATGTGAGCAGGCACTTTTGAGGTATAAGAAACTGTCAAGTGATTATTCACACTTCTGT CATGCTGATGTGAGCAGGCACTTTTGAGGTATGAGAAACTGTCAAGTGATTATTCACACTTCTGT T C ROR2 Ensembl:ENSG00000169071 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965985339 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26244465 RMVar_hsa_circ_322347 47117 RMVar_ID_47117 Human_SNP_ID_406854477 A-to-I Human chr9 - 91896600 91896600 91896600 AAGTCTCTTATTTCTTGGTGTCCAGTGAGGCAATTTCTCTAATGGGAACCAGAAGCAGAGAGAGT AAGTCTCTTATTTCTTGGTGTCCAGTGAGGCAGTTTCTCTAATGGGAACCAGAAGCAGAGAGAGT T C ROR2 Ensembl:ENSG00000169071 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913532613 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_322347 47118 RMVar_ID_47118 Human_SNP_ID_406865172 A-to-I Human chr9 - 91938276 91938276 91938276 AAAAAAATTTTTGTAAGAGAAAGAGTCTCACTATGTTGTTCAGACTGGTCTCCAACTCCCGGACT AAAAAAATTTTTGTAAGAGAAAGAGTCTCACTGTGTTGTTCAGACTGGTCTCCAACTCCCGGACT T C ROR2 Ensembl:ENSG00000169071 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs964119923 Functional Loss SNV dbSNP153 33..33 33 - - - 47119 RMVar_ID_47119 Human_SNP_ID_406865176 A-to-I Human chr9 - 91938287 91938287 91938287 GGCTAACTAAAAAAAAAATTTTTGTAAGAGAAAGAGTCTCACTATGTTGTTCAGACTGGTCTCCA GGCTAACTAAAAAAAAAATTTTTGTAAGAGAAGGAGTCTCACTATGTTGTTCAGACTGGTCTCCA T C ROR2 Ensembl:ENSG00000169071 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1247598016 Functional Loss SNV dbSNP153 33..33 33 - - - 47120 RMVar_ID_47120 Human_SNP_ID_406865178 A-to-I Human chr9 - 91938294 91938294 91938294 AACATCTGGCTAACTAAAAAAAAAATTTTTGTAAGAGAAAGAGTCTCACTATGTTGTTCAGACTG AACATCTGGCTAACTAAAAAAAAAATTTTTGTGAGAGAAAGAGTCTCACTATGTTGTTCAGACTG T C ROR2 Ensembl:ENSG00000169071 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs996622765 Functional Loss SNV dbSNP153 33..33 33 - - - 47121 RMVar_ID_47121 Human_SNP_ID_406865229 A-to-I Human chr9 - 91938500 91938500 91938500 CTCCTGCCTCACTCTCCCACATAGCTAAGATTACAGGTGTGCACATCACATCTGGCTCACATTTG CTCCTGCCTCACTCTCCCACATAGCTAAGATTGCAGGTGTGCACATCACATCTGGCTCACATTTG T C ROR2 Ensembl:ENSG00000169071 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs957543904 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16731686 47122 RMVar_ID_47122 Human_SNP_ID_406892539 A-to-I Human chr9 - 92052733 92052733 92052733 GAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTAAAACCCCGTCTCTACTAAAAATACAAA GAGGTCAGGAGTTCGAGACCAGCCTGGCCAACGTGGTAAAACCCCGTCTCTACTAAAAATACAAA T C SPTLC1 Ensembl:ENSG00000090054 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1177172901 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_347546,RMVar_hsa_circ_287555,RMVar_hsa_circ_34675,RMVar_hsa_circ_257754,RMVar_hsa_circ_257755,RMVar_hsa_circ_257756,RMVar_hsa_circ_96134,RMVar_hsa_circ_266244 47123 RMVar_ID_47123 Human_SNP_ID_406892556 A-to-I Human chr9 - 92052805 92052805 92052805 TAATCTGGCCGGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGTGA TAATCTGGCCGGGCACGGTGGCTCACGCCTGTGATCCCAGCACTTTGGGAGGCCGAGGCAGGTGA T C SPTLC1 Ensembl:ENSG00000090054 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs999072385 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5228575 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_347546,RMVar_hsa_circ_287555,RMVar_hsa_circ_34675,RMVar_hsa_circ_257754,RMVar_hsa_circ_257755,RMVar_hsa_circ_257756,RMVar_hsa_circ_96134,RMVar_hsa_circ_266244 47124 RMVar_ID_47124 Human_SNP_ID_406892557 A-to-I Human chr9 - 92052805 92052805 92052805 TAATCTGGCCGGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGTGA TAATCTGGCCGGGCACGGTGGCTCACGCCTGTCATCCCAGCACTTTGGGAGGCCGAGGCAGGTGA T G SPTLC1 Ensembl:ENSG00000090054 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs999072385 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5228575 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_347546,RMVar_hsa_circ_287555,RMVar_hsa_circ_34675,RMVar_hsa_circ_257754,RMVar_hsa_circ_257755,RMVar_hsa_circ_257756,RMVar_hsa_circ_96134,RMVar_hsa_circ_266244 47125 RMVar_ID_47125 Human_SNP_ID_406892858 A-to-I Human chr9 - 92054156 92054156 92054156 CTGCCTCAGCCTCCCAGGTAGCTGGGATTACAAGCATGTGCCACCATGCCCGGCTAATTTTGTAT CTGCCTCAGCCTCCCAGGTAGCTGGGATTACAGGCATGTGCCACCATGCCCGGCTAATTTTGTAT T C SPTLC1 Ensembl:ENSG00000090054 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1564090102 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_347546,RMVar_hsa_circ_287555,RMVar_hsa_circ_34675,RMVar_hsa_circ_257754,RMVar_hsa_circ_257755,RMVar_hsa_circ_257756,RMVar_hsa_circ_96134,RMVar_hsa_circ_266244 47126 RMVar_ID_47126 Human_SNP_ID_406892980 A-to-I Human chr9 - 92054669 92054669 92054669 ACCTCATGATCTGCCCGCCTGGGCCTCCCAAAATGCTGGGATTACAGGCATGAGCCACTGAGTCG ACCTCATGATCTGCCCGCCTGGGCCTCCCAAATTGCTGGGATTACAGGCATGAGCCACTGAGTCG T A SPTLC1 Ensembl:ENSG00000090054 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1564090399 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_347546,RMVar_hsa_circ_287555,RMVar_hsa_circ_34675,RMVar_hsa_circ_257754,RMVar_hsa_circ_257755,RMVar_hsa_circ_257756,RMVar_hsa_circ_96134,RMVar_hsa_circ_266244 47127 RMVar_ID_47127 Human_SNP_ID_406898657 A-to-I Human chr9 - 92079214 92079214 92079214 AAAATTAGCTGGGCGTGGTGGTGGATACCTGTAATCCCAGCTACGTGGGAGGCTGAGGTGGGAGA AAAATTAGCTGGGCGTGGTGGTGGATACCTGTGATCCCAGCTACGTGGGAGGCTGAGGTGGGAGA T C SPTLC1 Ensembl:ENSG00000090054 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1135525 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 47128 RMVar_ID_47128 Human_SNP_ID_406898660 A-to-I Human chr9 - 92079220 92079220 92079220 AATACAAAAATTAGCTGGGCGTGGTGGTGGATACCTGTAATCCCAGCTACGTGGGAGGCTGAGGT AATACAAAAATTAGCTGGGCGTGGTGGTGGATGCCTGTAATCCCAGCTACGTGGGAGGCTGAGGT T C SPTLC1 Ensembl:ENSG00000090054 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1135524 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 47129 RMVar_ID_47129 Human_SNP_ID_406898680 A-to-I Human chr9 - 92079269 92079269 92079269 GAGTTCAAAACCAGCCTGGCCAACATGCTGAAACCTCGTCTCTACTAAAAATACAAAAATTAGCT GAGTTCAAAACCAGCCTGGCCAACATGCTGAATCCTCGTCTCTACTAAAAATACAAAAATTAGCT T A SPTLC1 Ensembl:ENSG00000090054 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1265673674 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_182537 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 47130 RMVar_ID_47130 Human_SNP_ID_406898697 A-to-I Human chr9 - 92079348 92079348 92079348 GTTTAGGCCGGGCATGGTGGCTCATGCCTGTAATCCCAGCACTTTCAAAGGCTGAGGCAGGCAGA GTTTAGGCCGGGCATGGTGGCTCATGCCTGTAGTCCCAGCACTTTCAAAGGCTGAGGCAGGCAGA T C SPTLC1 Ensembl:ENSG00000090054 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170025124 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 47131 RMVar_ID_47131 Human_SNP_ID_406930461 A-to-I Human chr9 - 92210542 92210542 92210542 TACAATGTTACTTCAGCCCACAGTTTATTTCTATACTTGAGTTCTTAAGTACAGAAGATAGAAGT TACAATGTTACTTCAGCCCACAGTTTATTTCTGTACTTGAGTTCTTAAGTACAGAAGATAGAAGT T C IARS1 Ensembl:ENSG00000196305 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs937527137 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5535376,Human_RBP_ID_10438144,Human_RBP_ID_17322673,Human_RBP_ID_17437100,Human_RBP_ID_17550458,Human_RBP_ID_18400142,Human_RBP_ID_18911442,Human_RBP_ID_23216493 47132 RMVar_ID_47132 Human_SNP_ID_406937275 A-to-I Human chr9 - 92235623 92235623 92235623 ACTCAGGAGAGTAGGATTATTGAGGCAGGAGAATTGCTTGAACCTGGGAGGCAGAGGTTGCAGTG ACTCAGGAGAGTAGGATTATTGAGGCAGGAGACTTGCTTGAACCTGGGAGGCAGAGGTTGCAGTG T G IARS1 Ensembl:ENSG00000196305 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1389864412 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16733664 RMVar_hsa_circ_1206,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_88744,RMVar_hsa_circ_46434,RMVar_hsa_circ_38353,RMVar_hsa_circ_95691,RMVar_hsa_circ_257760,RMVar_hsa_circ_257762,RMVar_hsa_circ_257763,RMVar_hsa_circ_257764,RMVar_hsa_circ_257761,RMVar_hsa_circ_71967,RMVar_hsa_circ_372740,RMVar_hsa_circ_41770,RMVar_hsa_circ_77221,RMVar_hsa_circ_29001,RMVar_hsa_circ_257766,RMVar_hsa_circ_257768,RMVar_hsa_circ_257769,RMVar_hsa_circ_257767 47133 RMVar_ID_47133 Human_SNP_ID_406937418 A-to-I Human chr9 - 92236111 92236111 92236111 AGCCTGGTGGCGGGCGCCTGTAATCTCAGCCTACTCGGGAGGCTGAGGCAGGAGAATTGCTGTAA AGCCTGGTGGCGGGCGCCTGTAATCTCAGCCTGCTCGGGAGGCTGAGGCAGGAGAATTGCTGTAA T C IARS1 Ensembl:ENSG00000196305 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1473466640 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1206,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_88744,RMVar_hsa_circ_46434,RMVar_hsa_circ_38353,RMVar_hsa_circ_95691,RMVar_hsa_circ_257760,RMVar_hsa_circ_257762,RMVar_hsa_circ_257763,RMVar_hsa_circ_257764,RMVar_hsa_circ_257761,RMVar_hsa_circ_71967,RMVar_hsa_circ_372740,RMVar_hsa_circ_41770,RMVar_hsa_circ_77221,RMVar_hsa_circ_29001,RMVar_hsa_circ_257766,RMVar_hsa_circ_257768,RMVar_hsa_circ_257769,RMVar_hsa_circ_257767 47134 RMVar_ID_47134 Human_SNP_ID_406938446 A-to-I Human chr9 - 92240439 92240439 92240439 ATAAACATGGTGAAACCCTGTCTCTACTAAAAATACCAAAATTAGCCAGGCATGGTGGCAGGTAC ATAAACATGGTGAAACCCTGTCTCTACTAAAAGTACCAAAATTAGCCAGGCATGGTGGCAGGTAC T C IARS1 Ensembl:ENSG00000196305 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559125265 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1206,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_88744,RMVar_hsa_circ_46434,RMVar_hsa_circ_38353,RMVar_hsa_circ_95691,RMVar_hsa_circ_257760,RMVar_hsa_circ_257762,RMVar_hsa_circ_257763,RMVar_hsa_circ_257764,RMVar_hsa_circ_257761,RMVar_hsa_circ_71967,RMVar_hsa_circ_372740,RMVar_hsa_circ_41770,RMVar_hsa_circ_77221,RMVar_hsa_circ_29001,RMVar_hsa_circ_257766,RMVar_hsa_circ_257768,RMVar_hsa_circ_257769,RMVar_hsa_circ_257767 47135 RMVar_ID_47135 Human_SNP_ID_406938946 A-to-I Human chr9 - 92242218 92242218 92242218 AAGCCACACAGAGTTCATATTTACCACCATAAAGGCTCCCTTGAAACCATATCCAGTTTCTCCAT AAGCCACACAGAGTTCATATTTACCACCATAAGGGCTCCCTTGAAACCATATCCAGTTTCTCCAT T C IARS1 Ensembl:ENSG00000196305 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs773078041 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_287309,Human_RBP_ID_8929494,Human_RBP_ID_9239107,Human_RBP_ID_17322932,Human_RBP_ID_18139439,Human_RBP_ID_18400151,Human_RBP_ID_18911512,Human_RBP_ID_22838974,Human_RBP_ID_27787682 Human_Splice_Rec_1060835,Human_Splice_Rec_1060901,Human_Splice_Rec_1060969,Human_Splice_Rec_1061033,Human_Splice_Rec_1061047,Human_Splice_Rec_1061053,Human_Splice_Rec_1061057 Human_miRNA_ID_1465248,Human_miRNA_ID_2923639 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_88744,RMVar_hsa_circ_46434,RMVar_hsa_circ_95691,RMVar_hsa_circ_257760,RMVar_hsa_circ_257762,RMVar_hsa_circ_257763,RMVar_hsa_circ_257764,RMVar_hsa_circ_257761,RMVar_hsa_circ_71967,RMVar_hsa_circ_372740,RMVar_hsa_circ_41770,RMVar_hsa_circ_77221,RMVar_hsa_circ_29001,RMVar_hsa_circ_41218,RMVar_hsa_circ_70678,RMVar_hsa_circ_52048,RMVar_hsa_circ_257766,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_46188,RMVar_hsa_circ_50727,RMVar_hsa_circ_40256,RMVar_hsa_circ_257772,RMVar_hsa_circ_345438,RMVar_hsa_circ_372127,RMVar_hsa_circ_257770,RMVar_hsa_circ_365044,RMVar_hsa_circ_314649,RMVar_hsa_circ_257774,RMVar_hsa_circ_30506,RMVar_hsa_circ_36929,RMVar_hsa_circ_21654,RMVar_hsa_circ_257775,RMVar_hsa_circ_257773 47136 RMVar_ID_47136 Human_SNP_ID_406941845 A-to-I Human chr9 - 92253441 92253441 92253441 TTGACTTGTCTTACTTTTAGCTTATAGGCTTTATACTGTGGTGCCTCGCCTGGTCAAGTTTGTAG TTGACTTGTCTTACTTTTAGCTTATAGGCTTTGTACTGTGGTGCCTCGCCTGGTCAAGTTTGTAG T C IARS1 Ensembl:ENSG00000196305 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1347905402 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_91916,Human_RBP_ID_1707213,Human_RBP_ID_2066636,Human_RBP_ID_3225500,Human_RBP_ID_5033998,Human_RBP_ID_7946050,Human_RBP_ID_8708159,Human_RBP_ID_8929510,Human_RBP_ID_9314881,Human_RBP_ID_16734099,Human_RBP_ID_17716918,Human_RBP_ID_18139453,Human_RBP_ID_18911558,Human_RBP_ID_23093880,Human_RBP_ID_24312985,Human_RBP_ID_24563546,Human_RBP_ID_26235492,Human_RBP_ID_27787690 Human_Splice_Rec_1060818,Human_Splice_Rec_1060819,Human_Splice_Rec_1060884,Human_Splice_Rec_1060885,Human_Splice_Rec_1060952,Human_Splice_Rec_1060953,Human_Splice_Rec_1061016,Human_Splice_Rec_1061017 Human_miRNA_ID_2055603,Human_miRNA_ID_2067252,Human_miRNA_ID_2448511 RMVar_hsa_circ_32472,RMVar_hsa_circ_92786,RMVar_hsa_circ_280674,RMVar_hsa_circ_345342,RMVar_hsa_circ_110631,RMVar_hsa_circ_95691,RMVar_hsa_circ_257760,RMVar_hsa_circ_257762,RMVar_hsa_circ_257761,RMVar_hsa_circ_372740,RMVar_hsa_circ_77221,RMVar_hsa_circ_26951,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_40256,RMVar_hsa_circ_257772,RMVar_hsa_circ_345438,RMVar_hsa_circ_365044,RMVar_hsa_circ_46513,RMVar_hsa_circ_30506,RMVar_hsa_circ_257773,RMVar_hsa_circ_103565,RMVar_hsa_circ_70139,RMVar_hsa_circ_257777,RMVar_hsa_circ_109384,RMVar_hsa_circ_56996,RMVar_hsa_circ_257779,RMVar_hsa_circ_87454,RMVar_hsa_circ_257781,RMVar_hsa_circ_52301,RMVar_hsa_circ_47473,RMVar_hsa_circ_114960,RMVar_hsa_circ_81681,RMVar_hsa_circ_257783,RMVar_hsa_circ_112800,RMVar_hsa_circ_257784,RMVar_hsa_circ_257785,RMVar_hsa_circ_257788,RMVar_hsa_circ_109403,RMVar_hsa_circ_369373,RMVar_hsa_circ_257787 47137 RMVar_ID_47137 Human_SNP_ID_406943825 A-to-I Human chr9 - 92261181 92261181 92261181 TCTCAGCCTCCCGAGTAGCTGGGACCACAGGCATGAACCACCACACCCAGCTAATATTTTGTATT TCTCAGCCTCCCGAGTAGCTGGGACCACAGGCGTGAACCACCACACCCAGCTAATATTTTGTATT T C IARS1 Ensembl:ENSG00000196305 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs975562727 Functional Loss SNV dbSNP153 33..33 33 - - - 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_26951,RMVar_hsa_circ_257768,RMVar_hsa_circ_257769,RMVar_hsa_circ_67519,RMVar_hsa_circ_86655,RMVar_hsa_circ_126942,RMVar_hsa_circ_257771,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_114960,RMVar_hsa_circ_112800,RMVar_hsa_circ_257784,RMVar_hsa_circ_257785,RMVar_hsa_circ_257788,RMVar_hsa_circ_109403,RMVar_hsa_circ_369373,RMVar_hsa_circ_257787,RMVar_hsa_circ_34925,RMVar_hsa_circ_273589,RMVar_hsa_circ_290506,RMVar_hsa_circ_359241,RMVar_hsa_circ_376013,RMVar_hsa_circ_306852,RMVar_hsa_circ_45103,RMVar_hsa_circ_257792,RMVar_hsa_circ_257794,RMVar_hsa_circ_14667,RMVar_hsa_circ_257793,RMVar_hsa_circ_257791,RMVar_hsa_circ_12793,RMVar_hsa_circ_100982,RMVar_hsa_circ_364638,RMVar_hsa_circ_257795,RMVar_hsa_circ_257796,RMVar_hsa_circ_63220 47138 RMVar_ID_47138 Human_SNP_ID_406944011 A-to-I Human chr9 - 92261889 92261889 92261889 CAAAATTAGTGGGTGCAGTGGCACACACCTGTAACCCCAGCTACCTGGGAGGCTGAGGCACAAGA CAAAATTAGTGGGTGCAGTGGCACACACCTGTGACCCCAGCTACCTGGGAGGCTGAGGCACAAGA T C IARS1 Ensembl:ENSG00000196305 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs948285939 Functional Loss SNV dbSNP153 33..33 33 - - - 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_26951,RMVar_hsa_circ_257768,RMVar_hsa_circ_257769,RMVar_hsa_circ_67519,RMVar_hsa_circ_86655,RMVar_hsa_circ_126942,RMVar_hsa_circ_257771,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_114960,RMVar_hsa_circ_112800,RMVar_hsa_circ_257784,RMVar_hsa_circ_257785,RMVar_hsa_circ_257788,RMVar_hsa_circ_109403,RMVar_hsa_circ_369373,RMVar_hsa_circ_257787,RMVar_hsa_circ_34925,RMVar_hsa_circ_273589,RMVar_hsa_circ_290506,RMVar_hsa_circ_359241,RMVar_hsa_circ_376013,RMVar_hsa_circ_306852,RMVar_hsa_circ_45103,RMVar_hsa_circ_257792,RMVar_hsa_circ_257794,RMVar_hsa_circ_14667,RMVar_hsa_circ_257793,RMVar_hsa_circ_257791,RMVar_hsa_circ_12793,RMVar_hsa_circ_100982,RMVar_hsa_circ_364638,RMVar_hsa_circ_257795,RMVar_hsa_circ_257796,RMVar_hsa_circ_63220 47139 RMVar_ID_47139 Human_SNP_ID_406944015 A-to-I Human chr9 - 92261905 92261905 92261905 GTCTCTACTAAAAATACAAAATTAGTGGGTGCAGTGGCACACACCTGTAACCCCAGCTACCTGGG GTCTCTACTAAAAATACAAAATTAGTGGGTGCGGTGGCACACACCTGTAACCCCAGCTACCTGGG T C IARS1 Ensembl:ENSG00000196305 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs113164392 Functional Loss SNV dbSNP153 33..33 33 - - - 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_26951,RMVar_hsa_circ_257768,RMVar_hsa_circ_257769,RMVar_hsa_circ_67519,RMVar_hsa_circ_86655,RMVar_hsa_circ_126942,RMVar_hsa_circ_257771,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_114960,RMVar_hsa_circ_112800,RMVar_hsa_circ_257784,RMVar_hsa_circ_257785,RMVar_hsa_circ_257788,RMVar_hsa_circ_109403,RMVar_hsa_circ_369373,RMVar_hsa_circ_257787,RMVar_hsa_circ_34925,RMVar_hsa_circ_273589,RMVar_hsa_circ_290506,RMVar_hsa_circ_359241,RMVar_hsa_circ_376013,RMVar_hsa_circ_306852,RMVar_hsa_circ_45103,RMVar_hsa_circ_257792,RMVar_hsa_circ_257794,RMVar_hsa_circ_14667,RMVar_hsa_circ_257793,RMVar_hsa_circ_257791,RMVar_hsa_circ_12793,RMVar_hsa_circ_100982,RMVar_hsa_circ_364638,RMVar_hsa_circ_257795,RMVar_hsa_circ_257796,RMVar_hsa_circ_63220 47140 RMVar_ID_47140 Human_SNP_ID_406944017 A-to-I Human chr9 - 92261914 92261914 92261914 AAAACCCCCGTCTCTACTAAAAATACAAAATTAGTGGGTGCAGTGGCACACACCTGTAACCCCAG AAAACCCCCGTCTCTACTAAAAATACAAAATTTGTGGGTGCAGTGGCACACACCTGTAACCCCAG T A IARS1 Ensembl:ENSG00000196305 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs952174626 Functional Loss SNV dbSNP153 33..33 33 - - - 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_26951,RMVar_hsa_circ_257768,RMVar_hsa_circ_257769,RMVar_hsa_circ_67519,RMVar_hsa_circ_86655,RMVar_hsa_circ_126942,RMVar_hsa_circ_257771,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_114960,RMVar_hsa_circ_112800,RMVar_hsa_circ_257784,RMVar_hsa_circ_257785,RMVar_hsa_circ_257788,RMVar_hsa_circ_109403,RMVar_hsa_circ_369373,RMVar_hsa_circ_257787,RMVar_hsa_circ_34925,RMVar_hsa_circ_273589,RMVar_hsa_circ_290506,RMVar_hsa_circ_359241,RMVar_hsa_circ_376013,RMVar_hsa_circ_306852,RMVar_hsa_circ_45103,RMVar_hsa_circ_257792,RMVar_hsa_circ_257794,RMVar_hsa_circ_14667,RMVar_hsa_circ_257793,RMVar_hsa_circ_257791,RMVar_hsa_circ_12793,RMVar_hsa_circ_100982,RMVar_hsa_circ_364638,RMVar_hsa_circ_257795,RMVar_hsa_circ_257796,RMVar_hsa_circ_63220 47141 RMVar_ID_47141 Human_SNP_ID_406944896 A-to-I Human chr9 - 92265504 92265504 92265504 AGTGGCGGAACTTGAAGAACTGTCAGGAGCAAAGATCTCAGATCTCCACAGAGAGAGGTCAGTTT AGTGGCGGAACTTGAAGAACTGTCAGGAGCAAGGATCTCAGATCTCCACAGAGAGAGGTCAGTTT T C IARS1 Ensembl:ENSG00000196305 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1241262845 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_287310,Human_RBP_ID_1707350,Human_RBP_ID_2066680,Human_RBP_ID_3904701,Human_RBP_ID_3974582,Human_RBP_ID_5034038,Human_RBP_ID_5634267,Human_RBP_ID_8708211,Human_RBP_ID_8929528,Human_RBP_ID_16734690,Human_RBP_ID_18414497,Human_RBP_ID_18911633,Human_RBP_ID_19023946,Human_RBP_ID_22467341,Human_RBP_ID_22839029,Human_RBP_ID_24313039,Human_RBP_ID_24555381,Human_RBP_ID_26360808,Human_RBP_ID_26833297 Human_Splice_Rec_1060806,Human_Splice_Rec_1060807,Human_Splice_Rec_1060872,Human_Splice_Rec_1060873,Human_Splice_Rec_1060940,Human_Splice_Rec_1060941,Human_Splice_Rec_1061004,Human_Splice_Rec_1061005 Human_miRNA_ID_1984622,Human_miRNA_ID_2403771,Human_miRNA_ID_2940255 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_126942,RMVar_hsa_circ_257771,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_114960,RMVar_hsa_circ_112800,RMVar_hsa_circ_257784,RMVar_hsa_circ_257785,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_376013,RMVar_hsa_circ_306852,RMVar_hsa_circ_45103,RMVar_hsa_circ_257792,RMVar_hsa_circ_257794,RMVar_hsa_circ_257793,RMVar_hsa_circ_257791,RMVar_hsa_circ_12793,RMVar_hsa_circ_100982,RMVar_hsa_circ_364638,RMVar_hsa_circ_257795,RMVar_hsa_circ_257796,RMVar_hsa_circ_63220,RMVar_hsa_circ_30110,RMVar_hsa_circ_257798,RMVar_hsa_circ_283495,RMVar_hsa_circ_289656,RMVar_hsa_circ_362691,RMVar_hsa_circ_8235,RMVar_hsa_circ_280923,RMVar_hsa_circ_305132,RMVar_hsa_circ_84443,RMVar_hsa_circ_257799,RMVar_hsa_circ_257800,RMVar_hsa_circ_257801,RMVar_hsa_circ_48920,RMVar_hsa_circ_3342 47142 RMVar_ID_47142 Human_SNP_ID_406949526 A-to-I Human chr9 - 92283557 92283557 92283557 GGCTCATTGCACCCTCCTCCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGA GGCTCATTGCACCCTCCTCCCAGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGA T C IARS1 Ensembl:ENSG00000196305 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs919488229 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_280674,RMVar_hsa_circ_77221,RMVar_hsa_circ_3835,RMVar_hsa_circ_26951,RMVar_hsa_circ_257769,RMVar_hsa_circ_86655,RMVar_hsa_circ_40256,RMVar_hsa_circ_257772,RMVar_hsa_circ_345438,RMVar_hsa_circ_30506,RMVar_hsa_circ_257773,RMVar_hsa_circ_56996,RMVar_hsa_circ_52301,RMVar_hsa_circ_47473,RMVar_hsa_circ_257788,RMVar_hsa_circ_109403,RMVar_hsa_circ_290506,RMVar_hsa_circ_306852,RMVar_hsa_circ_257794,RMVar_hsa_circ_257793,RMVar_hsa_circ_100982,RMVar_hsa_circ_257795,RMVar_hsa_circ_30110,RMVar_hsa_circ_362691,RMVar_hsa_circ_24922,RMVar_hsa_circ_14352,RMVar_hsa_circ_313364,RMVar_hsa_circ_339542,RMVar_hsa_circ_3342,RMVar_hsa_circ_257803,RMVar_hsa_circ_257804,RMVar_hsa_circ_375951,RMVar_hsa_circ_257807,RMVar_hsa_circ_257808,RMVar_hsa_circ_372403,RMVar_hsa_circ_339618,RMVar_hsa_circ_362760,RMVar_hsa_circ_257809,RMVar_hsa_circ_257811,RMVar_hsa_circ_303056 47143 RMVar_ID_47143 Human_SNP_ID_406974538 A-to-I Human chr9 + 92387296 92387296 92387296 AGGGAGCCTGAGTGAGGCAGGAGAATTGCTTGAACCCAGGGGGTGGAGGTTGCAGTGAGCCGAGA AGGGAGCCTGAGTGAGGCAGGAGAATTGCTTGGACCCAGGGGGTGGAGGTTGCAGTGAGCCGAGA A G CENPP Ensembl:ENSG00000188312 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1465392130 Functional Loss SNV dbSNP153 33..33 33 - - - 47144 RMVar_ID_47144 Human_SNP_ID_406974540 A-to-I Human chr9 + 92387301 92387301 92387301 GCCTGAGTGAGGCAGGAGAATTGCTTGAACCCAGGGGGTGGAGGTTGCAGTGAGCCGAGATTGTG GCCTGAGTGAGGCAGGAGAATTGCTTGAACCCCGGGGGTGGAGGTTGCAGTGAGCCGAGATTGTG A C CENPP Ensembl:ENSG00000188312 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1201973654 Functional Loss SNV dbSNP153 33..33 33 - - - 47145 RMVar_ID_47145 Human_SNP_ID_406974694 A-to-I Human chr9 + 92387893 92387893 92387893 TAAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGACGACAGGTGCCCACCACCACGCCCA TAAAGCAATTCTCCTGCCTCAGCCTCCTGAGTGGCTGGGACGACAGGTGCCCACCACCACGCCCA A G CENPP Ensembl:ENSG00000188312 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1246946582 Functional Loss SNV dbSNP153 33..33 33 - - - 47146 RMVar_ID_47146 Human_SNP_ID_406974869 A-to-I Human chr9 + 92388670 92388669 92388670 CAAGACCAGCCTGGCCAACACCCATCTCTACTAAAAGTGTAGAAATTAGCCGGGCGTGGTGGTGT CAAGACCAGCCTGGCCAACACCCATCTCTACT_AAAGTGTAGAAATTAGCCGGGCGTGGTGGTGT TA T CENPP Ensembl:ENSG00000188312 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1395635234 Functional Loss DEL dbSNP153 33..33 33 - - - 47147 RMVar_ID_47147 Human_SNP_ID_406976949 A-to-I Human chr9 + 92397156 92397156 92397156 CCATGATCATGCCACTATACTCCAGCATGGGTAATAGAGCGAGACCCTGTCTAAAAAAACAAACA CCATGATCATGCCACTATACTCCAGCATGGGTTATAGAGCGAGACCCTGTCTAAAAAAACAAACA A T CENPP Ensembl:ENSG00000188312 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1257988048 Functional Loss SNV dbSNP153 33..33 33 - - - 47148 RMVar_ID_47148 Human_SNP_ID_406980141 A-to-I Human chr9 + 92412270 92412270 92412270 CACCATGCCTGGCTAATTTTTAATTTTTTTGTAGAGACAGGGTTTCACTGTGTTGCCTAGGCCAG CACCATGCCTGGCTAATTTTTAATTTTTTTGTCGAGACAGGGTTTCACTGTGTTGCCTAGGCCAG A C CENPP Ensembl:ENSG00000188312 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1408624732 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16737100 47149 RMVar_ID_47149 Human_SNP_ID_406981214 A-to-I Human chr9 + 92416309 92416309 92416309 TTTGGTAGAGATGGGACTTCACTATATTGACCAGGCTGATCTCGAACTCCTGGCCTCAAGTGATC TTTGGTAGAGATGGGACTTCACTATATTGACCGGGCTGATCTCGAACTCCTGGCCTCAAGTGATC A G CENPP Ensembl:ENSG00000188312 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs901233074 Functional Loss SNV dbSNP153 33..33 33 - - - 47150 RMVar_ID_47150 Human_SNP_ID_406984234 A-to-I Human chr9 + 92429772 92429772 92429772 TTGCACCATTGCACTCTGACCTGGGTGACAAGAACGAAACTCCGTCTCAAAATCATCATCATCAT TTGCACCATTGCACTCTGACCTGGGTGACAAGTACGAAACTCCGTCTCAAAATCATCATCATCAT A T CENPP Ensembl:ENSG00000188312 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1406216313 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16737422 47151 RMVar_ID_47151 Human_SNP_ID_406984425 A-to-I Human chr9 + 92430522 92430522 92430522 GGGATTACAGGCACCCACAACTACACCTGGCTAATTTTTGTATTGTAGTAGAGACAGGGTTTCAT GGGATTACAGGCACCCACAACTACACCTGGCTCATTTTTGTATTGTAGTAGAGACAGGGTTTCAT A C CENPP Ensembl:ENSG00000188312 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1280084470 Functional Loss SNV dbSNP153 33..33 33 - - - 47152 RMVar_ID_47152 Human_SNP_ID_406984445 A-to-I Human chr9 + 92430617 92430617 92430617 AACTCGGGTGATCTGCCCTCTTCGGCCTCCCAAAGTTCTGGGATTACAGGTGTGAGCCACCACGC AACTCGGGTGATCTGCCCTCTTCGGCCTCCCAGAGTTCTGGGATTACAGGTGTGAGCCACCACGC A G CENPP Ensembl:ENSG00000188312 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs906813969 Functional Loss SNV dbSNP153 33..33 33 - - - 47153 RMVar_ID_47153 Human_SNP_ID_406985081 A-to-I Human chr9 + 92433463 92433463 92433463 ATTACATTTGAGTTTTTGTAAGGCAGCCTGATACCTTTTTTTCTTCTCTAATGTGGGGAAAAGGT ATTACATTTGAGTTTTTGTAAGGCAGCCTGATGCCTTTTTTTCTTCTCTAATGTGGGGAAAAGGT A G CENPP Ensembl:ENSG00000188312 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1166475870 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3232736,Human_RBP_ID_7947081,Human_RBP_ID_10438659,Human_RBP_ID_16737474 47154 RMVar_ID_47154 Human_SNP_ID_406985144 A-to-I Human chr9 + 92433761 92433761 92433761 CGAGACCAGCGTGACCAACATGGCAAAACCCCATCTCTACTAGAACTACAAAAAGTAGCTGGGTA CGAGACCAGCGTGACCAACATGGCAAAACCCCGTCTCTACTAGAACTACAAAAAGTAGCTGGGTA A G CENPP Ensembl:ENSG00000188312 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1229092884 Functional Loss SNV dbSNP153 33..33 33 - - - 47155 RMVar_ID_47155 Human_SNP_ID_406985165 A-to-I Human chr9 + 92433833 92433833 92433833 GCTTGCCTGTAATCCCAGCTACTTGGGAGGCTAAGGCAGGAGAATCGCTTGAACCCGGGAGGCAG GCTTGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGGGAGGCAG A G CENPP Ensembl:ENSG00000188312 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs920633798 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16737479 47156 RMVar_ID_47156 Human_SNP_ID_406987378 A-to-I Human chr9 + 92443723 92443723 92443723 GCTCTGTCCCCCAGGCTGGAGTGCAGTGGCGCAATCTCGGCTCACTGCGACCTCCACCTCCCTGG GCTCTGTCCCCCAGGCTGGAGTGCAGTGGCGCCATCTCGGCTCACTGCGACCTCCACCTCCCTGG A C CENPP Ensembl:ENSG00000188312 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs752043475 Functional Loss SNV dbSNP153 33..33 33 - - - 47157 RMVar_ID_47157 Human_SNP_ID_407008184 A-to-I Human chr9 + 92537389 92537389 92537389 CTATTTTTAAAAATGTAAAACTAGCTGAGTGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGG CTATTTTTAAAAATGTAAAACTAGCTGAGTGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGG A G CENPP Ensembl:ENSG00000188312 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1468878196 Functional Loss SNV dbSNP153 33..33 33 - - - 47158 RMVar_ID_47158 Human_SNP_ID_407009352 A-to-I Human chr9 + 92542584 92542584 92542584 ATAGCTCCAGGCTATAGTGCAGTGGCACGATCATGGCTCACTGCAATCTCTGCCTCCCGGGTTCA ATAGCTCCAGGCTATAGTGCAGTGGCACGATCGTGGCTCACTGCAATCTCTGCCTCCCGGGTTCA A G CENPP Ensembl:ENSG00000188312 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1369588992 Functional Loss SNV dbSNP153 33..33 33 - - - 47159 RMVar_ID_47159 Human_SNP_ID_407011840 A-to-I Human chr9 + 92551431 92551431 92551431 ACAACCATGGCTTACTGTAGCTTCAACCTCCCAGGCTCAAACAATCCTCCCACCTTAGCCTGTCA ACAACCATGGCTTACTGTAGCTTCAACCTCCCGGGCTCAAACAATCCTCCCACCTTAGCCTGTCA A G CENPP Ensembl:ENSG00000188312 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1490318319 Functional Loss SNV dbSNP153 33..33 33 - - - 47160 RMVar_ID_47160 Human_SNP_ID_407018018 A-to-I Human chr9 + 92574818 92574818 92574818 GCTGGAGGACTCATTTCTTAATTTCAAAACTTACTACAAAGCTACAATAATCAAAACAATGTAGG GCTGGAGGACTCATTTCTTAATTTCAAAACTTGCTACAAAGCTACAATAATCAAAACAATGTAGG A G CENPP Ensembl:ENSG00000188312 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991414201 Functional Loss SNV dbSNP153 33..33 33 - - - 47161 RMVar_ID_47161 Human_SNP_ID_407018062 A-to-I Human chr9 + 92575050 92575050 92575050 GTATGAAGTTGGAACCTTAGCTAACACCATATACAAAAATTAACTCAAAATGGATCAAAGACCTA GTATGAAGTTGGAACCTTAGCTAACACCATATGCAAAAATTAACTCAAAATGGATCAAAGACCTA A G CENPP Ensembl:ENSG00000188312 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1029367718 Functional Loss SNV dbSNP153 33..33 33 - - - 47162 RMVar_ID_47162 Human_SNP_ID_407021301 A-to-I Human chr9 + 92588729 92588729 92588729 GAGAATCACTTCACACCCATTAAAATAGCTGTAATCAACAAAACGCAGACAATATCAAGTGCAGG GAGAATCACTTCACACCCATTAAAATAGCTGTGATCAACAAAACGCAGACAATATCAAGTGCAGG A G CENPP Ensembl:ENSG00000188312 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1419539120 Functional Loss SNV dbSNP153 33..33 33 - - - 47163 RMVar_ID_47163 Human_SNP_ID_407032573 A-to-I Human chr9 - 92635787 92635787 92635787 GGATCTTAGAAATTCCTTGCCTTGCAGTTGCAATGAGTCGAGATCACGCCACTGCACTCCAGGCT GGATCTTAGAAATTCCTTGCCTTGCAGTTGCAGTGAGTCGAGATCACGCCACTGCACTCCAGGCT T C IPPK Ensembl:ENSG00000127080 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs537906194 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16739551 RMVar_hsa_circ_9102,RMVar_hsa_circ_327803,RMVar_hsa_circ_339880,RMVar_hsa_circ_331570,RMVar_hsa_circ_299652 47164 RMVar_ID_47164 Human_SNP_ID_407036400 A-to-I Human chr9 - 92651757 92651757 92651757 TAGCTGAGATCACGCCACTGTACTCCAACCCCAGGTGACAGAGTGAGACTCCGTCTCAAACAAAC TAGCTGAGATCACGCCACTGTACTCCAACCCCGGGTGACAGAGTGAGACTCCGTCTCAAACAAAC T C IPPK Ensembl:ENSG00000127080 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941254130 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9102,RMVar_hsa_circ_339880,RMVar_hsa_circ_333407,RMVar_hsa_circ_339336,RMVar_hsa_circ_28733 47165 RMVar_ID_47165 Human_SNP_ID_407082540 A-to-I Human chr9 - 92840503 92840503 92840503 GGGACTACAGGCACACGCCACCACACCTGCTAATTTTTTTAGTTTTTTAGAGACAGGGTCTTGCT GGGACTACAGGCACACGCCACCACACCTGCTATTTTTTTTAGTTTTTTAGAGACAGGGTCTTGCT T A lnc-ZNF484-1 RNACentral:URS00008B8093 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1398025456 Functional Loss SNV dbSNP153 33..33 33 - - - 47166 RMVar_ID_47166 Human_SNP_ID_407148840 A-to-I Human chr9 + 93111459 93111459 93111459 GACCAGAGGGACTGGGCGGCTTGTCCCAGGCTACTGGGCTGTGGTCTCTGACCCCCTGGAGGCCT GACCAGAGGGACTGGGCGGCTTGTCCCAGGCTGCTGGGCTGTGGTCTCTGACCCCCTGGAGGCCT A G CARD19 Ensembl:ENSG00000165233 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs758304185 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27335 47167 RMVar_ID_47167 Human_SNP_ID_407157536 A-to-I Human chr9 + 93141709 93141709 93141709 TTGAACCTGGGAGGCAGAGGTTGCAGTGGGCCAAGAACTCACCATTGCACTCCAGCCTGGATGAC TTGAACCTGGGAGGCAGAGGTTGCAGTGGGCCGAGAACTCACCATTGCACTCCAGCCTGGATGAC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1341837439 Functional Loss SNV dbSNP153 33..33 33 - - - 47168 RMVar_ID_47168 Human_SNP_ID_407193767 A-to-I Human chr9 + 93280714 93280714 93280714 GATCCTTTCCCCAGGATTTGAGGCTGGGGCTTATTTTCTTCAGCACTGTGAGGACAGCACTATTC GATCCTTTCCCCAGGATTTGAGGCTGGGGCTTGTTTTCTTCAGCACTGTGAGGACAGCACTATTC A G WNK2 Ensembl:ENSG00000165238 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1281727139 Functional Loss SNV dbSNP153 33..33 33 - - - 47169 RMVar_ID_47169 Human_SNP_ID_407193768 A-to-I Human chr9 + 93280723 93280723 93280723 CCCAGGATTTGAGGCTGGGGCTTATTTTCTTCAGCACTGTGAGGACAGCACTATTCCTTGTCTAC CCCAGGATTTGAGGCTGGGGCTTATTTTCTTCGGCACTGTGAGGACAGCACTATTCCTTGTCTAC A G WNK2 Ensembl:ENSG00000165238 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs553226561 Functional Loss SNV dbSNP153 33..33 33 - - - 47170 RMVar_ID_47170 Human_SNP_ID_407194059 A-to-I Human chr9 + 93281932 93281932 93281932 ATCTGACTTCCATGAAGATGAAATGAAGAGAAAAGCAGTCATCACCTTCACAGCTCAATTAAAGA ATCTGACTTCCATGAAGATGAAATGAAGAGAAGAGCAGTCATCACCTTCACAGCTCAATTAAAGA A G WNK2 Ensembl:ENSG00000165238 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs890880776 Functional Loss SNV dbSNP153 33..33 33 - - - 47171 RMVar_ID_47171 Human_SNP_ID_407205298 A-to-I Human chr9 + 93323227 93323227 93323227 CCTGTAATCCCGGTGCTTTGGGAGGCTGAGGCAGGAGGATCACTTGAGGCCAAGAGGTCAAGGCT CCTGTAATCCCGGTGCTTTGGGAGGCTGAGGCGGGAGGATCACTTGAGGCCAAGAGGTCAAGGCT A G lnc-WNK2-1 RNACentral:URS00008BB2F8 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1312143041 Functional Loss SNV dbSNP153 33..33 33 - - - 47172 RMVar_ID_47172 Human_SNP_ID_407234473 A-to-I Human chr9 - 93448410 93448410 93448410 CAGCTCACTGCAACCTCCCTCTCCCAGGTTCAAGTGATCTCCTGCCTCAGCCTCTGGAGTAGCTG CAGCTCACTGCAACCTCCCTCTCCCAGGTTCAGGTGATCTCCTGCCTCAGCCTCTGGAGTAGCTG T C FAM120AOS Ensembl:ENSG00000188938 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1361861379 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1062621,Human_Splice_Rec_1062625,Human_Splice_Rec_1062629,Human_Splice_Rec_1062633 RMVar_hsa_circ_257859 47173 RMVar_ID_47173 Human_SNP_ID_407234484 A-to-I Human chr9 - 93448441 93448441 93448441 TTGCCCAGGCTGGAGTACAATGATGTGTTCTCAGCTCACTGCAACCTCCCTCTCCCAGGTTCAAG TTGCCCAGGCTGGAGTACAATGATGTGTTCTCGGCTCACTGCAACCTCCCTCTCCCAGGTTCAAG T C FAM120AOS Ensembl:ENSG00000188938 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1315202880 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1062621,Human_Splice_Rec_1062625,Human_Splice_Rec_1062629,Human_Splice_Rec_1062633 RMVar_hsa_circ_257859 47174 RMVar_ID_47174 Human_SNP_ID_407234490 A-to-I Human chr9 - 93448451 93448451 93448451 TCTTGCTCTGTTGCCCAGGCTGGAGTACAATGATGTGTTCTCAGCTCACTGCAACCTCCCTCTCC TCTTGCTCTGTTGCCCAGGCTGGAGTACAATGGTGTGTTCTCAGCTCACTGCAACCTCCCTCTCC T C FAM120AOS Ensembl:ENSG00000188938 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1244664195 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1062621,Human_Splice_Rec_1062625,Human_Splice_Rec_1062629,Human_Splice_Rec_1062633 RMVar_hsa_circ_257859 47175 RMVar_ID_47175 Human_SNP_ID_407234491 A-to-I Human chr9 - 93448454 93448454 93448454 GAGTCTTGCTCTGTTGCCCAGGCTGGAGTACAATGATGTGTTCTCAGCTCACTGCAACCTCCCTC GAGTCTTGCTCTGTTGCCCAGGCTGGAGTACAGTGATGTGTTCTCAGCTCACTGCAACCTCCCTC T C FAM120AOS Ensembl:ENSG00000188938 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs767541287 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1062621,Human_Splice_Rec_1062625,Human_Splice_Rec_1062629,Human_Splice_Rec_1062633 RMVar_hsa_circ_257859 47176 RMVar_ID_47176 Human_SNP_ID_407240634 A-to-I Human chr9 + 93473156 93473156 93473156 TCTCATGCCTCAGCCTCCTGAAAGCTGGGATTACAGGCGCCCACCACCACGCCCGGTTAATTTTT TCTCATGCCTCAGCCTCCTGAAAGCTGGGATTGCAGGCGCCCACCACCACGCCCGGTTAATTTTT A G FAM120A Ensembl:ENSG00000048828 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1358003995 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7948047 RMVar_hsa_circ_257864,RMVar_hsa_circ_115488,RMVar_hsa_circ_275590,RMVar_hsa_circ_302669,RMVar_hsa_circ_257861,RMVar_hsa_circ_257862,RMVar_hsa_circ_341422,RMVar_hsa_circ_357743,RMVar_hsa_circ_283821,RMVar_hsa_circ_293842,RMVar_hsa_circ_280773,RMVar_hsa_circ_273726,RMVar_hsa_circ_119641,RMVar_hsa_circ_257868,RMVar_hsa_circ_257872,RMVar_hsa_circ_85635,RMVar_hsa_circ_111731,RMVar_hsa_circ_257874,RMVar_hsa_circ_257873,RMVar_hsa_circ_257870,RMVar_hsa_circ_257871,RMVar_hsa_circ_257869,RMVar_hsa_circ_257866,RMVar_hsa_circ_257867,RMVar_hsa_circ_257865,RMVar_hsa_circ_257876,RMVar_hsa_circ_257863 47177 RMVar_ID_47177 Human_SNP_ID_407240700 A-to-I Human chr9 + 93473423 93473422 93473423 CACCTCCCAGGCTCAAGTGATCCTCCCATCTCAACTTCCCAAGTAGTTGGGACTACAGGTGCATG CACCTCCCAGGCTCAAGTGATCCTCCCATCTC_ACTTCCCAAGTAGTTGGGACTACAGGTGCATG CA C FAM120A Ensembl:ENSG00000048828 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs930068586 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_257864,RMVar_hsa_circ_115488,RMVar_hsa_circ_275590,RMVar_hsa_circ_302669,RMVar_hsa_circ_257861,RMVar_hsa_circ_257862,RMVar_hsa_circ_341422,RMVar_hsa_circ_357743,RMVar_hsa_circ_283821,RMVar_hsa_circ_293842,RMVar_hsa_circ_280773,RMVar_hsa_circ_273726,RMVar_hsa_circ_119641,RMVar_hsa_circ_257868,RMVar_hsa_circ_257872,RMVar_hsa_circ_85635,RMVar_hsa_circ_111731,RMVar_hsa_circ_257874,RMVar_hsa_circ_257873,RMVar_hsa_circ_257870,RMVar_hsa_circ_257871,RMVar_hsa_circ_257869,RMVar_hsa_circ_257866,RMVar_hsa_circ_257867,RMVar_hsa_circ_257865,RMVar_hsa_circ_257876,RMVar_hsa_circ_257863 47178 RMVar_ID_47178 Human_SNP_ID_407240701 A-to-I Human chr9 + 93473423 93473423 93473423 CACCTCCCAGGCTCAAGTGATCCTCCCATCTCAACTTCCCAAGTAGTTGGGACTACAGGTGCATG CACCTCCCAGGCTCAAGTGATCCTCCCATCTCTACTTCCCAAGTAGTTGGGACTACAGGTGCATG A T FAM120A Ensembl:ENSG00000048828 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs995108285 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_257864,RMVar_hsa_circ_115488,RMVar_hsa_circ_275590,RMVar_hsa_circ_302669,RMVar_hsa_circ_257861,RMVar_hsa_circ_257862,RMVar_hsa_circ_341422,RMVar_hsa_circ_357743,RMVar_hsa_circ_283821,RMVar_hsa_circ_293842,RMVar_hsa_circ_280773,RMVar_hsa_circ_273726,RMVar_hsa_circ_119641,RMVar_hsa_circ_257868,RMVar_hsa_circ_257872,RMVar_hsa_circ_85635,RMVar_hsa_circ_111731,RMVar_hsa_circ_257874,RMVar_hsa_circ_257873,RMVar_hsa_circ_257870,RMVar_hsa_circ_257871,RMVar_hsa_circ_257869,RMVar_hsa_circ_257866,RMVar_hsa_circ_257867,RMVar_hsa_circ_257865,RMVar_hsa_circ_257876,RMVar_hsa_circ_257863 47179 RMVar_ID_47179 Human_SNP_ID_407290457 A-to-I Human chr9 - 93676716 93676701 93676716 GTGGAGGCCGGGGTGGTGGAGGCCGGGGTGGTAGAGGCTGGCGTGGTGGAGGTGGAGGTGGTGCC GTGGAGGCCGGGGTGGTGGAGGCCGGGGTGGT_______________GGAGGTGGAGGTGGTGCC CACCACGCCAGCCTCT C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs768632985 Functional Loss DEL dbSNP153 33..47 33 - - - 47180 RMVar_ID_47180 Human_SNP_ID_407290473 A-to-I Human chr9 - 93676716 93676716 93676716 GTGGAGGCCGGGGTGGTGGAGGCCGGGGTGGTAGAGGCTGGCGTGGTGGAGGTGGAGGTGGTGCC GTGGAGGCCGGGGTGGTGGAGGCCGGGGTGGTGGAGGCTGGCGTGGTGGAGGTGGAGGTGGTGCC T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10821201 Functional Loss SNV dbSNP153 33..33 33 - - - 47181 RMVar_ID_47181 Human_SNP_ID_407411699 A-to-I Human chr9 + 94173173 94173173 94173173 CCCAGGAGGCGGAGGTTTCAGGAGCCAAGATCACACGGTTGCACTCCAGCCTGGGTGACAGAGCA CCCAGGAGGCGGAGGTTTCAGGAGCCAAGATCGCACGGTTGCACTCCAGCCTGGGTGACAGAGCA A G MIRLET7A1HG Ensembl:ENSG00000269929 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1262229959 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10439446,Human_RBP_ID_26244686 47182 RMVar_ID_47182 Human_SNP_ID_407411872 A-to-I Human chr9 + 94173775 94173775 94173775 CTTACTGCAACCTTTAACTCCTAGGCTCAAGCAATCTTCCTGCCTCAACCTCCTGAGTAACTCAG CTTACTGCAACCTTTAACTCCTAGGCTCAAGCCATCTTCCTGCCTCAACCTCCTGAGTAACTCAG A C MIRLET7A1HG Ensembl:ENSG00000269929 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1293114771 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5251855 47183 RMVar_ID_47183 Human_SNP_ID_407480263 A-to-I Human chr9 + 94453275 94453275 94453275 GGGTTCAAGTGATTCTACTGCCTCAGCCTCCCAAATAGCTGGGACTACAAGTGTGCACCACTATG GGGTTCAAGTGATTCTACTGCCTCAGCCTCCCGAATAGCTGGGACTACAAGTGTGCACCACTATG A G MFSD14B Ensembl:ENSG00000148110 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs888700050 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97542,RMVar_hsa_circ_120700,RMVar_hsa_circ_257924,RMVar_hsa_circ_257925,RMVar_hsa_circ_101750,RMVar_hsa_circ_106156,RMVar_hsa_circ_99098,RMVar_hsa_circ_16479,RMVar_hsa_circ_257933,RMVar_hsa_circ_257934,RMVar_hsa_circ_257932,RMVar_hsa_circ_38027,RMVar_hsa_circ_94358,RMVar_hsa_circ_336951,RMVar_hsa_circ_57859,RMVar_hsa_circ_257939,RMVar_hsa_circ_257935,RMVar_hsa_circ_257936,RMVar_hsa_circ_280988,RMVar_hsa_circ_345861 47184 RMVar_ID_47184 Human_SNP_ID_407500415 A-to-I Human chr9 - 94524349 94524346 94524350 AAAATTGAGATTAAGAGAGACATAGGCCAGGCACAGTGGCTCACGCCTGTAATCCCAGCACTTTG AAAATTGAGATTAAGAGAGACATAGGCCAGG____GTGGCTCACGCCTGTAATCCCAGCACTTTG CTGTG C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1281249765 Functional Loss DEL dbSNP153 32..35 33 - - - 47185 RMVar_ID_47185 Human_SNP_ID_407500416 A-to-I Human chr9 - 94524347 94524347 94524347 AATTGAGATTAAGAGAGACATAGGCCAGGCACAGTGGCTCACGCCTGTAATCCCAGCACTTTGGG AATTGAGATTAAGAGAGACATAGGCCAGGCACCGTGGCTCACGCCTGTAATCCCAGCACTTTGGG T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1231996228 Functional Loss SNV dbSNP153 33..33 33 - - - 47186 RMVar_ID_47186 Human_SNP_ID_407564638 A-to-I Human chr9 + 94776582 94776582 94776582 CCTCGGCCTCCCAAAGTGCTAAGATTACAGGCATGAGCCACTGCGCCCGACCTTTCCTCATTATG CCTCGGCCTCCCAAAGTGCTAAGATTACAGGCGTGAGCCACTGCGCCCGACCTTTCCTCATTATG A G AOPEP Ensembl:ENSG00000148120 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs578222012 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_257943,RMVar_hsa_circ_113784,RMVar_hsa_circ_344993,RMVar_hsa_circ_257941,RMVar_hsa_circ_111269,RMVar_hsa_circ_7660,RMVar_hsa_circ_83560,RMVar_hsa_circ_257942,RMVar_hsa_circ_273650,RMVar_hsa_circ_74210,RMVar_hsa_circ_257944,RMVar_hsa_circ_257945 47187 RMVar_ID_47187 Human_SNP_ID_407590344 A-to-I Human chr9 + 94888536 94888535 94888536 CAGCAGTTATGTTGTAGTCTTGTCAATGTATCAAGATGTACTAGTCTGTCGTTGTCTGAGATGGT CAGCAGTTATGTTGTAGTCTTGTCAATGTATC_AGATGTACTAGTCTGTCGTTGTCTGAGATGGT CA C AOPEP Ensembl:ENSG00000148120 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1245838604 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_113784,RMVar_hsa_circ_257941,RMVar_hsa_circ_111269,RMVar_hsa_circ_7660,RMVar_hsa_circ_83560,RMVar_hsa_circ_257942,RMVar_hsa_circ_257945 47188 RMVar_ID_47188 Human_SNP_ID_407590345 A-to-I Human chr9 + 94888536 94888536 94888536 CAGCAGTTATGTTGTAGTCTTGTCAATGTATCAAGATGTACTAGTCTGTCGTTGTCTGAGATGGT CAGCAGTTATGTTGTAGTCTTGTCAATGTATCCAGATGTACTAGTCTGTCGTTGTCTGAGATGGT A C AOPEP Ensembl:ENSG00000148120 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs75265315 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113784,RMVar_hsa_circ_257941,RMVar_hsa_circ_111269,RMVar_hsa_circ_7660,RMVar_hsa_circ_83560,RMVar_hsa_circ_257942,RMVar_hsa_circ_257945 47189 RMVar_ID_47189 Human_SNP_ID_407618740 A-to-I Human chr9 + 95011463 95011463 95011463 TGACCTCGTGATCCGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGACATGAGCCACCGCGC TGACCTCGTGATCCGCCCACCTCGGCCTCCCACAGTGCTGGGATTACAGACATGAGCCACCGCGC A C AOPEP Ensembl:ENSG00000148120 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs561962424 Functional Loss SNV dbSNP153 33..33 33 - - - 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_73834 47190 RMVar_ID_47190 Human_SNP_ID_407621384 A-to-I Human chr9 + 95021752 95021752 95021752 CCATCTTAGATTGAAGCTACATCGCTGTGTGCATCTAACTCTTGATTCACGGTCTGACCGACGCC CCATCTTAGATTGAAGCTACATCGCTGTGTGCGTCTAACTCTTGATTCACGGTCTGACCGACGCC A G AOPEP Ensembl:ENSG00000148120 Protein coding intron GSE100210;GSE99789 HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 29129909,29796672 RNA-Seq:(High) rs566777869 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18912159,Human_RBP_ID_24392950 Human_Splice_Rec_1063394,Human_Splice_Rec_1063406 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 47191 RMVar_ID_47191 Human_SNP_ID_407647534 A-to-I Human chr9 - 95123208 95123208 95123208 CCTTTGGCTTCGTGGGCTCAAGCGATCCCCCCACCTCAGCCTCCCAAGTAGTTGGGACCACAGGT CCTTTGGCTTCGTGGGCTCAAGCGATCCCCCCCCCTCAGCCTCCCAAGTAGTTGGGACCACAGGT T G FANCC Ensembl:ENSG00000158169 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1310127394 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_345453,RMVar_hsa_circ_11708,RMVar_hsa_circ_18640,RMVar_hsa_circ_257965 47192 RMVar_ID_47192 Human_SNP_ID_407647616 A-to-I Human chr9 - 95123457 95123457 95123457 TTTTGTATTTTTATTAGAGATGGGGTTTCACCATGTTGCCCGGGCTGGTCTCAACCTCTGAGGCT TTTTGTATTTTTATTAGAGATGGGGTTTCACCCTGTTGCCCGGGCTGGTCTCAACCTCTGAGGCT T G FANCC Ensembl:ENSG00000158169 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1040481410 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_345453,RMVar_hsa_circ_11708,RMVar_hsa_circ_18640,RMVar_hsa_circ_257965 47193 RMVar_ID_47193 Human_SNP_ID_407664537 A-to-I Human chr9 - 95191478 95191478 95191478 CCTATAGAAGTAGGATGCTGGCCAGGTGTGGTAGCCCATGCCTGTAATTCCAGCACTTTGGGAGG CCTATAGAAGTAGGATGCTGGCCAGGTGTGGTGGCCCATGCCTGTAATTCCAGCACTTTGGGAGG T C FANCC Ensembl:ENSG00000158169 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1367999082 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18640,RMVar_hsa_circ_20309,RMVar_hsa_circ_298529,RMVar_hsa_circ_340873,RMVar_hsa_circ_299596,RMVar_hsa_circ_257972,RMVar_hsa_circ_257970,RMVar_hsa_circ_257971,RMVar_hsa_circ_320201,RMVar_hsa_circ_305743 47194 RMVar_ID_47194 Human_SNP_ID_407666248 A-to-I Human chr9 - 95198803 95198803 95198803 AGCCCAGGAGGTGGAGGCTGTAATAAGCTGTAATGGCGCCACTGCACTCCAGTCTGGACCTGTTT AGCCCAGGAGGTGGAGGCTGTAATAAGCTGTAGTGGCGCCACTGCACTCCAGTCTGGACCTGTTT T C FANCC Ensembl:ENSG00000158169 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs905759772 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1146644 RMVar_hsa_circ_18640,RMVar_hsa_circ_20309,RMVar_hsa_circ_298529,RMVar_hsa_circ_340873,RMVar_hsa_circ_299596,RMVar_hsa_circ_257972,RMVar_hsa_circ_257970,RMVar_hsa_circ_257971,RMVar_hsa_circ_320201,RMVar_hsa_circ_305743 47195 RMVar_ID_47195 Human_SNP_ID_407712687 A-to-I Human chr9 - 95394209 95394209 95394209 GTTGGAGTGCAATGGCACGATCTCGACTCACCACAACCTCCACCTCCTGGTTTCAAGCGATTCTC GTTGGAGTGCAATGGCACGATCTCGACTCACCGCAACCTCCACCTCCTGGTTTCAAGCGATTCTC T C FANCC Ensembl:ENSG00000158169 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs899344876 Functional Loss SNV dbSNP153 33..33 33 - - - 47196 RMVar_ID_47196 Human_SNP_ID_407818176 A-to-I Human chr9 - 95812809 95812809 95812809 CAGGCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCCTGGCTCGTACACTGTTTTATA CAGGCTCCCAAAGTGCTGGGATTACAGGCGTGGGCCACCGCGCCTGGCTCGTACACTGTTTTATA T C LINC00476 Ensembl:ENSG00000175611 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1409816650 Functional Loss SNV dbSNP153 33..33 33 - - - 47197 RMVar_ID_47197 Human_SNP_ID_407818355 A-to-I Human chr9 - 95813509 95813509 95813509 AAGGCGGATGGATCACCTGAGGTCACGAGTTCAAGACCAGCCTGACCAACATGGAGAAATCCCAT AAGGCGGATGGATCACCTGAGGTCACGAGTTCCAGACCAGCCTGACCAACATGGAGAAATCCCAT T G LINC00476 Ensembl:ENSG00000175611 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1251862599 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_185651 47198 RMVar_ID_47198 Human_SNP_ID_407818371 A-to-I Human chr9 - 95813562 95813562 95813562 CTAGGGGCTGGGCGCGGTGGCTCTCGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGATGGA CTAGGGGCTGGGCGCGGTGGCTCTCGCCTGTATTCCCAGCACTTTGGGAGGCCAAGGCGGATGGA T A LINC00476 Ensembl:ENSG00000175611 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1383773854 Functional Loss SNV dbSNP153 33..33 33 - - - 47199 RMVar_ID_47199 Human_SNP_ID_407824910 A-to-I Human chr9 - 95842672 95842672 95842672 CGGCTCACTGCAAACTCTGCCTCCCGGGTTCAAGCGATTCTCCTCCCTCAGCCTCCTGAGTAGCT CGGCTCACTGCAAACTCTGCCTCCCGGGTTCAGGCGATTCTCCTCCCTCAGCCTCCTGAGTAGCT T C LINC00476 Ensembl:ENSG00000175611 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs929179002 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1064218,Human_Splice_Rec_1064224 47200 RMVar_ID_47200 Human_SNP_ID_407829642 A-to-I Human chr9 - 95864164 95864164 95864164 GCGCAATCGGCTCACTGCAACCTCTGCCTCCCAGTGTCAAGCGATTCTCCTGCCTCAGCCTCCCA GCGCAATCGGCTCACTGCAACCTCTGCCTCCCGGTGTCAAGCGATTCTCCTGCCTCAGCCTCCCA T C LINC00476 Ensembl:ENSG00000175611 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs996913591 Functional Loss SNV dbSNP153 33..33 33 - - - 47201 RMVar_ID_47201 Human_SNP_ID_407832512 A-to-I Human chr9 - 95875697 95875697 95875697 GGAGGCCGGCAAGGCGACCCCCAAATCTTCCTAGGCTCTGACTTCCGTCTCCTAACCCCCGCAAA GGAGGCCGGCAAGGCGACCCCCAAATCTTCCTGGGCTCTGACTTCCGTCTCCTAACCCCCGCAAA T C LINC00476 Ensembl:ENSG00000175611 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1262360422 Functional Loss SNV dbSNP153 33..33 33 - - - 47202 RMVar_ID_47202 Human_SNP_ID_407832520 A-to-I Human chr9 - 95875706 95875706 95875706 AGGAGGACAGGAGGCCGGCAAGGCGACCCCCAAATCTTCCTAGGCTCTGACTTCCGTCTCCTAAC AGGAGGACAGGAGGCCGGCAAGGCGACCCCCAGATCTTCCTAGGCTCTGACTTCCGTCTCCTAAC T C LINC00476 Ensembl:ENSG00000175611 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1466043689 Functional Loss SNV dbSNP153 33..33 33 - - - 47203 RMVar_ID_47203 Human_SNP_ID_407835215 A-to-I Human chr9 + 95886074 95886074 95886074 GTCTCACTCTGGCATTCAGGGTGGAGTGCAGTAGCGAGATCTCGGCTCACTGCAAAGTCCACCTC GTCTCACTCTGGCATTCAGGGTGGAGTGCAGTGGCGAGATCTCGGCTCACTGCAAAGTCCACCTC A G ERCC6L2 Ensembl:ENSG00000182150 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1326233995 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25440,RMVar_hsa_circ_348806,RMVar_hsa_circ_359122,RMVar_hsa_circ_341558,RMVar_hsa_circ_53922,RMVar_hsa_circ_64842,RMVar_hsa_circ_41913,RMVar_hsa_circ_257982,RMVar_hsa_circ_257983,RMVar_hsa_circ_257981 47204 RMVar_ID_47204 Human_SNP_ID_407866029 A-to-I Human chr9 + 96015388 96015388 96015388 TTTTGTGTTTTTAGTAGGGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTCAATCTCCTGGCTG TTTTGTGTTTTTAGTAGGGATGGGGTTTCACCCTGTTGGCCAGGCTGGTCTCAATCTCCTGGCTG A C ERCC6L2 Ensembl:ENSG00000182150 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs898133582 Functional Loss SNV dbSNP153 33..33 33 - - - 47205 RMVar_ID_47205 Human_SNP_ID_407949976 A-to-I Human chr9 - 96354692 96354692 96354692 TGCGATCTTGGCTACTGCAACCTCTGCTTCCTAGGTTCAAGCAATTGTCCTGCCTTAGTCTCCCA TGCGATCTTGGCTACTGCAACCTCTGCTTCCTGGGTTCAAGCAATTGTCCTGCCTTAGTCTCCCA T C SLC35D2 Ensembl:ENSG00000130958 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs571537850 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_334684,RMVar_hsa_circ_355797,RMVar_hsa_circ_336817,RMVar_hsa_circ_353497,RMVar_hsa_circ_360136,RMVar_hsa_circ_258022,RMVar_hsa_circ_102187,RMVar_hsa_circ_258024,RMVar_hsa_circ_347447,RMVar_hsa_circ_355642,RMVar_hsa_circ_317082,RMVar_hsa_circ_258025,RMVar_hsa_circ_18065 47206 RMVar_ID_47206 Human_SNP_ID_407976896 A-to-I Human chr9 + 96457211 96457211 96457211 CAGGTTAGAGAAACGTCGTCTCTACTGAAAATACAACATTAGCCAGGCGTGGTGGCGCAGGCCTG CAGGTTAGAGAAACGTCGTCTCTACTGAAAATGCAACATTAGCCAGGCGTGGTGGCGCAGGCCTG A G HABP4 Ensembl:ENSG00000130956 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs922444398 Functional Loss SNV dbSNP153 33..33 33 - - - 47207 RMVar_ID_47207 Human_SNP_ID_407978277 A-to-I Human chr9 + 96462831 96462831 96462831 GTAGTCTCAGCTGCTTGGGGGACTGACATGGGAAGATTGTTTGAGCCTGGGAGATCAAGGCTGCA GTAGTCTCAGCTGCTTGGGGGACTGACATGGGCAGATTGTTTGAGCCTGGGAGATCAAGGCTGCA A C HABP4 Ensembl:ENSG00000130956 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs775572536 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22484668 RMVar_hsa_circ_287102,RMVar_hsa_circ_301979,RMVar_hsa_circ_351305,RMVar_hsa_circ_32195,RMVar_hsa_circ_284344,RMVar_hsa_circ_258037,RMVar_hsa_circ_258038,RMVar_hsa_circ_258036 47208 RMVar_ID_47208 Human_SNP_ID_407982862 A-to-I Human chr9 + 96482206 96482206 96482206 ATGATCCGCCTGCCTCAGCCTCCCAAAGTGCTAGGATTACAGGCTTGAGCCACTGTGCCTGGCCT ATGATCCGCCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCTTGAGCCACTGTGCCTGGCCT A G HABP4 Ensembl:ENSG00000130956 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs546774941 Functional Loss SNV dbSNP153 33..33 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 47209 RMVar_ID_47209 Human_SNP_ID_407990340 A-to-I Human chr9 - 96512524 96512524 96512524 GGCCAGAATTTTGAGAATAGCCTGGGCAACATAGCGAGACCCCATCTCTATAAAATAAAAAATGA GGCCAGAATTTTGAGAATAGCCTGGGCAACATGGCGAGACCCCATCTCTATAAAATAAAAAATGA T C CDC14B Ensembl:ENSG00000081377 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1367365140 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10179,RMVar_hsa_circ_77065,RMVar_hsa_circ_328914,RMVar_hsa_circ_291825,RMVar_hsa_circ_32964,RMVar_hsa_circ_258044,RMVar_hsa_circ_258045 47210 RMVar_ID_47210 Human_SNP_ID_407990344 A-to-I Human chr9 - 96512561 96512561 96512561 CCAACACTTTGGAAGGTCGAGGAAAGAGAATCACTGAGGCCAGAATTTTGAGAATAGCCTGGGCA CCAACACTTTGGAAGGTCGAGGAAAGAGAATCGCTGAGGCCAGAATTTTGAGAATAGCCTGGGCA T C CDC14B Ensembl:ENSG00000081377 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs545474601 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10179,RMVar_hsa_circ_77065,RMVar_hsa_circ_328914,RMVar_hsa_circ_291825,RMVar_hsa_circ_32964,RMVar_hsa_circ_258044,RMVar_hsa_circ_258045 47211 RMVar_ID_47211 Human_SNP_ID_407990360 A-to-I Human chr9 - 96512600 96512600 96512600 ATTTTTAGGGATGGGCAGACTGGCTCATGCCTATAAATCCCAACACTTTGGAAGGTCGAGGAAAG ATTTTTAGGGATGGGCAGACTGGCTCATGCCTTTAAATCCCAACACTTTGGAAGGTCGAGGAAAG T A CDC14B Ensembl:ENSG00000081377 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,frontal_cortex - 29129909,30559470 RNA-Seq:(High) rs893105801 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10179,RMVar_hsa_circ_77065,RMVar_hsa_circ_328914,RMVar_hsa_circ_291825,RMVar_hsa_circ_32964,RMVar_hsa_circ_258044,RMVar_hsa_circ_258045 47212 RMVar_ID_47212 Human_SNP_ID_407990361 A-to-I Human chr9 - 96512600 96512600 96512600 ATTTTTAGGGATGGGCAGACTGGCTCATGCCTATAAATCCCAACACTTTGGAAGGTCGAGGAAAG ATTTTTAGGGATGGGCAGACTGGCTCATGCCTGTAAATCCCAACACTTTGGAAGGTCGAGGAAAG T C CDC14B Ensembl:ENSG00000081377 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,frontal_cortex - 29129909,30559470 RNA-Seq:(High) rs893105801 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10179,RMVar_hsa_circ_77065,RMVar_hsa_circ_328914,RMVar_hsa_circ_291825,RMVar_hsa_circ_32964,RMVar_hsa_circ_258044,RMVar_hsa_circ_258045 47213 RMVar_ID_47213 Human_SNP_ID_407991208 A-to-I Human chr9 - 96516604 96516604 96516604 GTGGTGATGTGCGCCTCTAATCCCAACTACTCAGGAGGCTGCAGTGGGAGAATTGTTTGAACCTG GTGGTGATGTGCGCCTCTAATCCCAACTACTCCGGAGGCTGCAGTGGGAGAATTGTTTGAACCTG T G CDC14B Ensembl:ENSG00000081377 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1175791417 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10179,RMVar_hsa_circ_77065,RMVar_hsa_circ_328914,RMVar_hsa_circ_291825,RMVar_hsa_circ_258047,RMVar_hsa_circ_39713,RMVar_hsa_circ_126917,RMVar_hsa_circ_258044,RMVar_hsa_circ_258045,RMVar_hsa_circ_336097,RMVar_hsa_circ_371329,RMVar_hsa_circ_270203,RMVar_hsa_circ_113107,RMVar_hsa_circ_22829,RMVar_hsa_circ_31498,RMVar_hsa_circ_258049,RMVar_hsa_circ_258048,RMVar_hsa_circ_258046 47214 RMVar_ID_47214 Human_SNP_ID_408008328 A-to-I Human chr9 - 96587001 96586999 96587001 GCCCGGTTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCGCGGTGTTGGCCAGGCTAGTCTCGA GCCCGGTTAATTTTTGTATTTTTAGTAGAGAC__GGTTTCGCGGTGTTGGCCAGGCTAGTCTCGA CCT C CDC14B Ensembl:ENSG00000081377 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1021404627 Functional Loss DEL dbSNP153 33..34 33 - - - 47215 RMVar_ID_47215 Human_SNP_ID_408008329 A-to-I Human chr9 - 96587001 96587001 96587001 GCCCGGTTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCGCGGTGTTGGCCAGGCTAGTCTCGA GCCCGGTTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCGCGGTGTTGGCCAGGCTAGTCTCGA T C CDC14B Ensembl:ENSG00000081377 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968430891 Functional Loss SNV dbSNP153 33..33 33 - - - 47216 RMVar_ID_47216 Human_SNP_ID_408008330 A-to-I Human chr9 - 96587001 96587001 96587001 GCCCGGTTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCGCGGTGTTGGCCAGGCTAGTCTCGA GCCCGGTTAATTTTTGTATTTTTAGTAGAGACCGGGTTTCGCGGTGTTGGCCAGGCTAGTCTCGA T G CDC14B Ensembl:ENSG00000081377 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968430891 Functional Loss SNV dbSNP153 33..33 33 - - - 47217 RMVar_ID_47217 Human_SNP_ID_408013147 A-to-I Human chr9 - 96606211 96606211 96606211 CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCACACATCACCACACCCGCTTATTTTTG CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTGCAGGCACACATCACCACACCCGCTTATTTTTG T C CDC14B Ensembl:ENSG00000081377 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1179482960 Functional Loss SNV dbSNP153 33..33 33 - - - 47218 RMVar_ID_47218 Human_SNP_ID_408013583 A-to-I Human chr9 - 96607532 96607532 96607532 CCTGTAGTCCCAGCTACTCAGGCGGCTGAGGCAGGAGAATGGCGTGAACCCTGGAAGCGGAGCTT CCTGTAGTCCCAGCTACTCAGGCGGCTGAGGCGGGAGAATGGCGTGAACCCTGGAAGCGGAGCTT T C CDC14B Ensembl:ENSG00000081377 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1466956114 Functional Loss SNV dbSNP153 33..33 33 - - - 47219 RMVar_ID_47219 Human_SNP_ID_408022980 A-to-I Human chr9 - 96644669 96644669 96644669 TCCAGACCAGCCCTTGGTGAAACCCCATCTCTACTAAAAGTACAAAAAATTAGCCGGGCGTGGTG TCCAGACCAGCCCTTGGTGAAACCCCATCTCTTCTAAAAGTACAAAAAATTAGCCGGGCGTGGTG T A PRXL2C Ensembl:ENSG00000158122 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1331682050 Functional Loss SNV dbSNP153 33..33 33 - - - 47220 RMVar_ID_47220 Human_SNP_ID_408043110 A-to-I Human chr9 + 96726641 96726641 96726641 ACTTGCTGTGCAGCGCAGCAAGGACGTGGTGTATGGGATCTGCATGGAGGTGGTCTATGAGAAAG ACTTGCTGTGCAGCGCAGCAAGGACGTGGTGTGTGGGATCTGCATGGAGGTGGTCTATGAGAAAG A G AL589843.2,AL589843.1 Ensembl:ENSG00000233820,Ensembl:ENSG00000224848 Pseudogene,lincRNA exon,intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs910409680 Functional Loss SNV dbSNP153 33..33 33 - - - 47221 RMVar_ID_47221 Human_SNP_ID_408051581 A-to-I Human chr9 - 96763215 96763213 96763215 CTGGTCTAAGTCCTCGATTGTGTTTTATTAACAGGGTACTGCTGTTTCAAACCAGAGGTGATCTT CTGGTCTAAGTCCTCGATTGTGTTTTATTAAC__GGTACTGCTGTTTCAAACCAGAGGTGATCTT CCT C ZNF510 Ensembl:ENSG00000081386 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs774797810 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_22690061 Human_Splice_Rec_1065313,Human_Splice_Rec_1065323 RMVar_hsa_circ_74377,RMVar_hsa_circ_288094,RMVar_hsa_circ_308050,RMVar_hsa_circ_258063,RMVar_hsa_circ_258064 47222 RMVar_ID_47222 Human_SNP_ID_408056497 A-to-I Human chr9 - 96782895 96782895 96782895 TTTTCCTGTGCTCTTCTCTCTCCTGCCGCCATATGAATAAGGTCCTTGCTTCCCCCTCACCTTCC TTTTCCTGTGCTCTTCTCTCTCCTGCCGCCATGTGAATAAGGTCCTTGCTTCCCCCTCACCTTCC T C lnc-MFSD14C-4 RNACentral:URS00009B48EC lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs756538984 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_258067 47223 RMVar_ID_47223 Human_SNP_ID_408078561 A-to-I Human chr9 - 96879381 96879381 96879381 CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCCGCCACCAGGCACGGCTAATTTTT CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTGCAGGCGCCCGCCACCAGGCACGGCTAATTTTT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1484936334 Functional Loss SNV dbSNP153 33..33 33 - - - 47224 RMVar_ID_47224 Human_SNP_ID_408083609 A-to-I Human chr9 - 96899108 96899108 96899108 AAGTTAAATAACTCAGTCATAAAAGGAAAAATACTATATGATTCGACTTATAGGAGGTACCTAGA AAGTTAAATAACTCAGTCATAAAAGGAAAAATGCTATATGATTCGACTTATAGGAGGTACCTAGA T C MFSD14C Ensembl:ENSG00000196312 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909254684 Functional Loss SNV dbSNP153 33..33 33 - - - 47225 RMVar_ID_47225 Human_SNP_ID_408083820 A-to-I Human chr9 - 96900032 96900032 96900032 CACTTTGGGAGGTCAAGGTCAGAGGATTGCTTAAGCCCAGGAGTTTGAGACCAGCCTGGGCAACG CACTTTGGGAGGTCAAGGTCAGAGGATTGCTTGAGCCCAGGAGTTTGAGACCAGCCTGGGCAACG T C MFSD14C Ensembl:ENSG00000196312 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs113556248 Functional Loss SNV dbSNP153 33..33 33 - - - 47226 RMVar_ID_47226 Human_SNP_ID_408087073 A-to-I Human chr9 - 96912480 96912478 96912480 CTCTGGCCTTTTTGTTTTTGAGATGGAAACTCACTCTGTCGCCCGGGCTGGAGTGCAGTGGCACG CTCTGGCCTTTTTGTTTTTGAGATGGAAACTC__TCTGTCGCCCGGGCTGGAGTGCAGTGGCACG AGT A MFSD14C Ensembl:ENSG00000196312 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1338787647 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_8709327 47227 RMVar_ID_47227 Human_SNP_ID_408091671 A-to-I Human chr9 - 96931032 96931032 96931032 ATACAAAAATTAGCTGATGATGCGTGCCTGTAATCGCAGCTACTCAGGAGGCTGAGACAGGAGAA ATACAAAAATTAGCTGATGATGCGTGCCTGTAGTCGCAGCTACTCAGGAGGCTGAGACAGGAGAA T C MFSD14C Ensembl:ENSG00000196312 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1367747666 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_272755 47228 RMVar_ID_47228 Human_SNP_ID_408095812 A-to-I Human chr9 - 96943596 96943596 96943596 CACCATGCCCAGCTGATTTTTGTATTTTTAGTAGAGGCGGGGTTTCACCATGTTGGCCAGGCTGG CACCATGCCCAGCTGATTTTTGTATTTTTAGTGGAGGCGGGGTTTCACCATGTTGGCCAGGCTGG T C MFSD14C Ensembl:ENSG00000196312 Pseudogene intron GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line - 24183664,31158229 RNA-Seq:(High) rs1489294684 Functional Loss SNV dbSNP153 33..33 33 - - - 47229 RMVar_ID_47229 Human_SNP_ID_408096545 A-to-I Human chr9 - 96946262 96946262 96946262 TTGAGGTCAGAAGTTTGAGACCAGCCTGGCCAACATGGTGAAACCTCATCTCTTCTAAAAATCCA TTGAGGTCAGAAGTTTGAGACCAGCCTGGCCATCATGGTGAAACCTCATCTCTTCTAAAAATCCA T A MFSD14C Ensembl:ENSG00000196312 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs555482955 Functional Loss SNV dbSNP153 33..33 33 - - - 47230 RMVar_ID_47230 Human_SNP_ID_408096546 A-to-I Human chr9 - 96946262 96946262 96946262 TTGAGGTCAGAAGTTTGAGACCAGCCTGGCCAACATGGTGAAACCTCATCTCTTCTAAAAATCCA TTGAGGTCAGAAGTTTGAGACCAGCCTGGCCAGCATGGTGAAACCTCATCTCTTCTAAAAATCCA T C MFSD14C Ensembl:ENSG00000196312 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs555482955 Functional Loss SNV dbSNP153 33..33 33 - - - 47231 RMVar_ID_47231 Human_SNP_ID_408096547 A-to-I Human chr9 - 96946263 96946263 96946263 CTTGAGGTCAGAAGTTTGAGACCAGCCTGGCCAACATGGTGAAACCTCATCTCTTCTAAAAATCC CTTGAGGTCAGAAGTTTGAGACCAGCCTGGCCGACATGGTGAAACCTCATCTCTTCTAAAAATCC T C MFSD14C Ensembl:ENSG00000196312 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1232347041 Functional Loss SNV dbSNP153 33..33 33 - - - 47232 RMVar_ID_47232 Human_SNP_ID_408096568 A-to-I Human chr9 - 96946332 96946332 96946332 ATTTTAAGCCAGATGCGGTAGCTCAAGCCTGTAATCCCAGCACTCTGGGAGGCCAAAGCAGGTGG ATTTTAAGCCAGATGCGGTAGCTCAAGCCTGTCATCCCAGCACTCTGGGAGGCCAAAGCAGGTGG T G MFSD14C Ensembl:ENSG00000196312 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1358706308 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17579321,Human_RBP_ID_23316852 47233 RMVar_ID_47233 Human_SNP_ID_408096571 A-to-I Human chr9 - 96946339 96946339 96946339 AAAAACAATTTTAAGCCAGATGCGGTAGCTCAAGCCTGTAATCCCAGCACTCTGGGAGGCCAAAG AAAAACAATTTTAAGCCAGATGCGGTAGCTCAGGCCTGTAATCCCAGCACTCTGGGAGGCCAAAG T C MFSD14C Ensembl:ENSG00000196312 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs146858874 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17579321 47234 RMVar_ID_47234 Human_SNP_ID_408096637 A-to-I Human chr9 - 96946558 96946558 96946558 TACCACGTCCGGCTAATTTTTTTTGTATTTCTAGTAGAAACGGGGTTTCACCATGTCAGCCAGGA TACCACGTCCGGCTAATTTTTTTTGTATTTCTGGTAGAAACGGGGTTTCACCATGTCAGCCAGGA T C MFSD14C Ensembl:ENSG00000196312 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1341509135 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26244812 47235 RMVar_ID_47235 Human_SNP_ID_408096649 A-to-I Human chr9 - 96946602 96946602 96946602 CTCTGGCCTCAGCCTCCCGAGTAGCTGGGACTATAGGAGCCCACTACCACGTCCGGCTAATTTTT CTCTGGCCTCAGCCTCCCGAGTAGCTGGGACTGTAGGAGCCCACTACCACGTCCGGCTAATTTTT T C MFSD14C Ensembl:ENSG00000196312 Pseudogene intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1396490858 Functional Loss SNV dbSNP153 33..33 33 - - - 47236 RMVar_ID_47236 Human_SNP_ID_408096662 A-to-I Human chr9 - 96946661 96946661 96946661 GGAGTGCAGTGGCGCGATCTCTGCTCACTGCAAGCTCAGCGTCCTGGGTTCATACCATTCTCTGG GGAGTGCAGTGGCGCGATCTCTGCTCACTGCAGGCTCAGCGTCCTGGGTTCATACCATTCTCTGG T C MFSD14C Ensembl:ENSG00000196312 Pseudogene intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs575920343 Functional Loss SNV dbSNP153 33..33 33 - - - 47237 RMVar_ID_47237 Human_SNP_ID_408096663 A-to-I Human chr9 - 96946661 96946661 96946661 GGAGTGCAGTGGCGCGATCTCTGCTCACTGCAAGCTCAGCGTCCTGGGTTCATACCATTCTCTGG GGAGTGCAGTGGCGCGATCTCTGCTCACTGCACGCTCAGCGTCCTGGGTTCATACCATTCTCTGG T G MFSD14C Ensembl:ENSG00000196312 Pseudogene intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs575920343 Functional Loss SNV dbSNP153 33..33 33 - - - 47238 RMVar_ID_47238 Human_SNP_ID_408096815 A-to-I Human chr9 - 96947106 96947106 96947106 TAGTCATAGTCTGGCTGGAGTGCAATGGCGCAATCTCAGCTCACTGCAACCTCCGCCTCCTGGGT TAGTCATAGTCTGGCTGGAGTGCAATGGCGCAGTCTCAGCTCACTGCAACCTCCGCCTCCTGGGT T C MFSD14C Ensembl:ENSG00000196312 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1383009284 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1228202 47239 RMVar_ID_47239 Human_SNP_ID_408096820 A-to-I Human chr9 - 96947114 96947114 96947114 TAGGACTATAGTCATAGTCTGGCTGGAGTGCAATGGCGCAATCTCAGCTCACTGCAACCTCCGCC TAGGACTATAGTCATAGTCTGGCTGGAGTGCAGTGGCGCAATCTCAGCTCACTGCAACCTCCGCC T C MFSD14C Ensembl:ENSG00000196312 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs534018533 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1228202,Human_RBP_ID_16754637 47240 RMVar_ID_47240 Human_SNP_ID_408141224 A-to-I Human chr9 - 97132052 97132052 97132052 TGGGACGGTGCTGCCCAGGGTGGGTGGCCGGGACCTGACAGCAGTACCCCAGGCAGTGACCACAT TGGGACGGTGCTGCCCAGGGTGGGTGGCCGGGGCCTGACAGCAGTACCCCAGGCAGTGACCACAT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1156781600 Functional Loss SNV dbSNP153 33..33 33 - - - 47241 RMVar_ID_47241 Human_SNP_ID_408142119 A-to-I Human chr9 - 97135750 97135750 97135750 CCAACAGCTTGTACCATCAGTTGTGAAAAGCTACATGCACTCAACACCAGCGCTGCCCATGGGGG CCAACAGCTTGTACCATCAGTTGTGAAAAGCTGCATGCACTCAACACCAGCGCTGCCCATGGGGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984985859 Functional Loss SNV dbSNP153 33..33 33 - - - 47242 RMVar_ID_47242 Human_SNP_ID_408142254 A-to-I Human chr9 - 97136313 97136313 97136313 AAATGGTCAAAAAGAAAAGCTGATTTTCTGGGAGAAAATTTAGGAAGGCTTCAGAAATTTGCATA AAATGGTCAAAAAGAAAAGCTGATTTTCTGGGGGAAAATTTAGGAAGGCTTCAGAAATTTGCATA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1288084396 Functional Loss SNV dbSNP153 33..33 33 - - - 47243 RMVar_ID_47243 Human_SNP_ID_408142790 A-to-I Human chr9 - 97138847 97138847 97138847 ACCAACAGCTTGCACCCTCAGTGTGGAAAGCTACAGGTGCTCAACACTAGCCCAGCCCATGAGGG ACCAACAGCTTGCACCCTCAGTGTGGAAAGCTGCAGGTGCTCAACACTAGCCCAGCCCATGAGGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1487916260 Functional Loss SNV dbSNP153 33..33 33 - - - 47244 RMVar_ID_47244 Human_SNP_ID_408142821 A-to-I Human chr9 - 97138928 97138928 97138928 AGGGTAGTACAGAAGGAACATATGGAGTTGGAATCCCCACACATGGAGGCACCATTCTGCAAACC AGGGTAGTACAGAAGGAACATATGGAGTTGGAGTCCCCACACATGGAGGCACCATTCTGCAAACC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1453379380 Functional Loss SNV dbSNP153 33..33 33 - - - 47245 RMVar_ID_47245 Human_SNP_ID_408143584 A-to-I Human chr9 - 97142514 97142514 97142514 GGAAAATTCAAGACAGCTTCAGAAACTTGCATAAAATGGAGCCCAGTGCTAATAGCCAAGACAAT GGAAAATTCAAGACAGCTTCAGAAACTTGCATGAAATGGAGCCCAGTGCTAATAGCCAAGACAAT T C lnc-CTSV-6,lnc-CTSV-6:2 RNACentral:URS00009B4993,RNACentral:URS00008BD6B7 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs756800039 Functional Loss SNV dbSNP153 33..33 33 - - - 47246 RMVar_ID_47246 Human_SNP_ID_408145135 A-to-I Human chr9 - 97149333 97149333 97149333 CACAAAATTAGTGCTGTGAAGTGGAGCTATGAAATGCCTTCAGAGCCTTTTCCACATTATCTTGG CACAAAATTAGTGCTGTGAAGTGGAGCTATGAGATGCCTTCAGAGCCTTTTCCACATTATCTTGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1362420151 Functional Loss SNV dbSNP153 33..33 33 - - - 47247 RMVar_ID_47247 Human_SNP_ID_408163045 A-to-I Human chr9 - 97227665 97227665 97227665 TTGTATTTTTAGTAGAGACAGGGTTTCACCATATTGGCCAGGCTGGTCTTGAACTTTGGGACTCA TTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTTTGGGACTCA T C AL590705.1 Ensembl:ENSG00000203279 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs201028756 Functional Loss SNV dbSNP153 33..33 33 - - - 47248 RMVar_ID_47248 Human_SNP_ID_408168603 A-to-I Human chr9 + 97252063 97252063 97252063 AGTAACTTTTAATTTTATTTTTTTTAAAAGACAGTGTCTTGCTCTGTTACACAGGCTGGAGTGCA AGTAACTTTTAATTTTATTTTTTTTAAAAGACGGTGTCTTGCTCTGTTACACAGGCTGGAGTGCA A G SUGT1P4-STRA6LP,STRA6LP Ensembl:ENSG00000254876,Ensembl:ENSG00000255036 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1406121529 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75650,RMVar_hsa_circ_258084 47249 RMVar_ID_47249 Human_SNP_ID_408215791 A-to-I Human chr9 + 97451050 97451050 97451050 CCCAACCAACCTCTGGGGAAGGTAGAGGGCCTAAAGATTAGGTTGATCGCCAGTGGCCAATGACT CCCAACCAACCTCTGGGGAAGGTAGAGGGCCTGAAGATTAGGTTGATCGCCAGTGGCCAATGACT A G TDRD7 Ensembl:ENSG00000196116 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1046759373 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9019,RMVar_hsa_circ_11355,RMVar_hsa_circ_33232,RMVar_hsa_circ_21895 47250 RMVar_ID_47250 Human_SNP_ID_408251451 A-to-I Human chr9 + 97600982 97600982 97600982 TTTCAGCAAATCTCATGATAAAGGACAAGGTCAAGAACTCCAGAGCACTGAGCAGAGAGGCTGGT TTTCAGCAAATCTCATGATAAAGGACAAGGTCTAGAACTCCAGAGCACTGAGCAGAGAGGCTGGT A T TMOD1 Ensembl:ENSG00000136842 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs896987033 Functional Loss SNV dbSNP153 33..33 33 - - - 47251 RMVar_ID_47251 Human_SNP_ID_408251848 A-to-I Human chr9 + 97602542 97602542 97602542 GCTCTGGGCTCACAGGCTGTCGCACATGCTGCAAGAGTTCCCTAGGTATGCGTGGCCGTCGGGCT GCTCTGGGCTCACAGGCTGTCGCACATGCTGCGAGAGTTCCCTAGGTATGCGTGGCCGTCGGGCT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749218582 Functional Loss SNV dbSNP153 33..33 33 - - - 47252 RMVar_ID_47252 Human_SNP_ID_408258590 A-to-I Human chr9 - 97631762 97631762 97631762 TTGGCTCGTTGTAACCTCTGCCTTTTAGGTTCAGGCAATTCTTGTGCCTTAGCCACCCAAGTAGC TTGGCTCGTTGTAACCTCTGCCTTTTAGGTTCGGGCAATTCTTGTGCCTTAGCCACCCAAGTAGC T C TSTD2 Ensembl:ENSG00000136925 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs570305373 Functional Loss SNV dbSNP153 33..33 33 - - - 47253 RMVar_ID_47253 Human_SNP_ID_408264782 A-to-I Human chr9 + 97656394 97656394 97656394 ACATGATGTGAGGAGTTCAGGCTAGCATGGCCAACATGGGGAAACCCCCTCTCTACTAAAAATAA ACATGATGTGAGGAGTTCAGGCTAGCATGGCCGACATGGGGAAACCCCCTCTCTACTAAAAATAA A G NCBP1 Ensembl:ENSG00000136937 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1260534220 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_258117,RMVar_hsa_circ_89529,RMVar_hsa_circ_82341,RMVar_hsa_circ_79551,RMVar_hsa_circ_122817,RMVar_hsa_circ_125370,RMVar_hsa_circ_82408,RMVar_hsa_circ_258123,RMVar_hsa_circ_258124,RMVar_hsa_circ_258121,RMVar_hsa_circ_258122,RMVar_hsa_circ_343169,RMVar_hsa_circ_266279,RMVar_hsa_circ_369854,RMVar_hsa_circ_121221,RMVar_hsa_circ_119800,RMVar_hsa_circ_258131,RMVar_hsa_circ_258132,RMVar_hsa_circ_258130,RMVar_hsa_circ_258140,RMVar_hsa_circ_78224,RMVar_hsa_circ_95143,RMVar_hsa_circ_322992,RMVar_hsa_circ_373909,RMVar_hsa_circ_22473,RMVar_hsa_circ_258143,RMVar_hsa_circ_258144,RMVar_hsa_circ_18696,RMVar_hsa_circ_71213,RMVar_hsa_circ_258145 47254 RMVar_ID_47254 Human_SNP_ID_408264801 A-to-I Human chr9 + 97656458 97656458 97656458 AAAATTTGCGAGGCGTGTTGGCGAACGTCTATAATCCCAGCTACTTGGGAGGTTGAGGGAGAGTC AAAATTTGCGAGGCGTGTTGGCGAACGTCTATGATCCCAGCTACTTGGGAGGTTGAGGGAGAGTC A G NCBP1 Ensembl:ENSG00000136937 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1422210646 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_258117,RMVar_hsa_circ_89529,RMVar_hsa_circ_82341,RMVar_hsa_circ_79551,RMVar_hsa_circ_122817,RMVar_hsa_circ_125370,RMVar_hsa_circ_82408,RMVar_hsa_circ_258123,RMVar_hsa_circ_258124,RMVar_hsa_circ_258121,RMVar_hsa_circ_258122,RMVar_hsa_circ_343169,RMVar_hsa_circ_266279,RMVar_hsa_circ_369854,RMVar_hsa_circ_121221,RMVar_hsa_circ_119800,RMVar_hsa_circ_258131,RMVar_hsa_circ_258132,RMVar_hsa_circ_258130,RMVar_hsa_circ_258140,RMVar_hsa_circ_78224,RMVar_hsa_circ_95143,RMVar_hsa_circ_322992,RMVar_hsa_circ_373909,RMVar_hsa_circ_22473,RMVar_hsa_circ_258143,RMVar_hsa_circ_258144,RMVar_hsa_circ_18696,RMVar_hsa_circ_71213,RMVar_hsa_circ_258145 47255 RMVar_ID_47255 Human_SNP_ID_408264809 A-to-I Human chr9 + 97656500 97656500 97656500 ACTTGGGAGGTTGAGGGAGAGTCCTTTGAGCCAAGATGGCGCCACTGCACTCCAATCTGGCCGAC ACTTGGGAGGTTGAGGGAGAGTCCTTTGAGCCGAGATGGCGCCACTGCACTCCAATCTGGCCGAC A G NCBP1 Ensembl:ENSG00000136937 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs975811602 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16518479 RMVar_hsa_circ_258117,RMVar_hsa_circ_89529,RMVar_hsa_circ_82341,RMVar_hsa_circ_79551,RMVar_hsa_circ_122817,RMVar_hsa_circ_125370,RMVar_hsa_circ_82408,RMVar_hsa_circ_258123,RMVar_hsa_circ_258124,RMVar_hsa_circ_258121,RMVar_hsa_circ_258122,RMVar_hsa_circ_343169,RMVar_hsa_circ_266279,RMVar_hsa_circ_369854,RMVar_hsa_circ_121221,RMVar_hsa_circ_119800,RMVar_hsa_circ_258131,RMVar_hsa_circ_258132,RMVar_hsa_circ_258130,RMVar_hsa_circ_258140,RMVar_hsa_circ_78224,RMVar_hsa_circ_95143,RMVar_hsa_circ_322992,RMVar_hsa_circ_373909,RMVar_hsa_circ_22473,RMVar_hsa_circ_258143,RMVar_hsa_circ_258144,RMVar_hsa_circ_18696,RMVar_hsa_circ_71213,RMVar_hsa_circ_258145 47256 RMVar_ID_47256 Human_SNP_ID_408266931 A-to-I Human chr9 + 97665042 97665042 97665042 TATTTATGAAGTTCACGGACTTTACAGCTGATAGGACCAGGGCAGCAGGAGTTGACACAAAGCAG TATTTATGAAGTTCACGGACTTTACAGCTGATGGGACCAGGGCAGCAGGAGTTGACACAAAGCAG A G NCBP1 Ensembl:ENSG00000136937 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs765440617 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16518732 RMVar_hsa_circ_258117,RMVar_hsa_circ_89529,RMVar_hsa_circ_79551,RMVar_hsa_circ_125370,RMVar_hsa_circ_82408,RMVar_hsa_circ_258123,RMVar_hsa_circ_258121,RMVar_hsa_circ_258122,RMVar_hsa_circ_266279,RMVar_hsa_circ_369854,RMVar_hsa_circ_7254,RMVar_hsa_circ_119800,RMVar_hsa_circ_258130,RMVar_hsa_circ_258140,RMVar_hsa_circ_78224,RMVar_hsa_circ_95143,RMVar_hsa_circ_258144,RMVar_hsa_circ_258145,RMVar_hsa_circ_1744,RMVar_hsa_circ_258147 47257 RMVar_ID_47257 Human_SNP_ID_408268246 A-to-I Human chr9 - 97670193 97670193 97670193 AATTAGGAGACTGGGCACCGTGGCTCACGCCTATAATCCCAGCAGCACTTTGGGAGGCGGAGGCC AATTAGGAGACTGGGCACCGTGGCTCACGCCTGTAATCCCAGCAGCACTTTGGGAGGCGGAGGCC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs757381147 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16518770 47258 RMVar_ID_47258 Human_SNP_ID_408268247 A-to-I Human chr9 - 97670193 97670193 97670193 AATTAGGAGACTGGGCACCGTGGCTCACGCCTATAATCCCAGCAGCACTTTGGGAGGCGGAGGCC AATTAGGAGACTGGGCACCGTGGCTCACGCCTCTAATCCCAGCAGCACTTTGGGAGGCGGAGGCC T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs757381147 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16518770 47259 RMVar_ID_47259 Human_SNP_ID_408268901 A-to-I Human chr9 + 97672945 97672945 97672945 GGTCAGGAGATTGAGACCATCCTGGCTAACACAGTGAAACCCTGTCTCTACTAAAAACACAAAAA GGTCAGGAGATTGAGACCATCCTGGCTAACACGGTGAAACCCTGTCTCTACTAAAAACACAAAAA A G NCBP1 Ensembl:ENSG00000136937 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs977836923 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82408,RMVar_hsa_circ_258121,RMVar_hsa_circ_266279 47260 RMVar_ID_47260 Human_SNP_ID_408270251 A-to-I Human chr9 - 97677649 97677649 97677649 CTCTGTCACCTAGGCTGGAGTGCAGTGGTGCAATCATGGCTCACTGCAGGCTCAAACTCCTCGGC CTCTGTCACCTAGGCTGGAGTGCAGTGGTGCACTCATGGCTCACTGCAGGCTCAAACTCCTCGGC T G XPA Ensembl:ENSG00000136936 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs887145808 Functional Loss SNV dbSNP153 33..33 33 - - - 47261 RMVar_ID_47261 Human_SNP_ID_408270414 A-to-I Human chr9 + 97678236 97678236 97678236 CAGCTTGGCCAATATGGTGAAACCCCATCTCTACTGAAAACACAAAAATTAGCTGGACATGGTGG CAGCTTGGCCAATATGGTGAAACCCCATCTCTCCTGAAAACACAAAAATTAGCTGGACATGGTGG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs949129586 Functional Loss SNV dbSNP153 33..33 33 - - - 47262 RMVar_ID_47262 Human_SNP_ID_408270885 A-to-I Human chr9 + 97680278 97680278 97680278 TTGCCCAGGCTGGAGTGCAATGGGGGGATCTCAGCTCACTGCAACCTCCACTTCCCAGGTTCAAG TTGCCCAGGCTGGAGTGCAATGGGGGGATCTCGGCTCACTGCAACCTCCACTTCCCAGGTTCAAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs999592306 Functional Loss SNV dbSNP153 33..33 33 - - - 47263 RMVar_ID_47263 Human_SNP_ID_408273329 A-to-I Human chr9 - 97690276 97690276 97690276 AACCCGAGAGGTGGAGGTTACACTGAGCTGAGATCGTGCCACTGCACTCCAGCCTGGGTGGCAGA AACCCGAGAGGTGGAGGTTACACTGAGCTGAGGTCGTGCCACTGCACTCCAGCCTGGGTGGCAGA T C XPA Ensembl:ENSG00000136936 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1160607306 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_258151,RMVar_hsa_circ_350887,RMVar_hsa_circ_327705,RMVar_hsa_circ_258152 47264 RMVar_ID_47264 Human_SNP_ID_408273622 A-to-I Human chr9 - 97691536 97691536 97691536 TGACACCTGGCTAATTTTTGGATTTTTTTTGTAGAGACAGGGCTTTGCCATGTTGACCAGGCTGG TGACACCTGGCTAATTTTTGGATTTTTTTTGTGGAGACAGGGCTTTGCCATGTTGACCAGGCTGG T C XPA Ensembl:ENSG00000136936 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1047074213 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16519144 RMVar_hsa_circ_258151,RMVar_hsa_circ_350887,RMVar_hsa_circ_327705,RMVar_hsa_circ_258152 47265 RMVar_ID_47265 Human_SNP_ID_408273670 A-to-I Human chr9 - 97691761 97691761 97691761 CTCTTACCTCAGCCTCCCAAGTAGCTGGGACTACAGGCACACACTACCATGCCTGGCTAATTTTT CTCTTACCTCAGCCTCCCAAGTAGCTGGGACTGCAGGCACACACTACCATGCCTGGCTAATTTTT T C XPA Ensembl:ENSG00000136936 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs920083042 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_258151,RMVar_hsa_circ_350887,RMVar_hsa_circ_327705,RMVar_hsa_circ_258152 47266 RMVar_ID_47266 Human_SNP_ID_408308414 A-to-I Human chr9 - 97844098 97844098 97844098 CCTCCACCCTCAAGTAGGCTCCAGTTTCTGTTATTTCCTTCTTTGTGTCCATGAATTCTCATAAT CCTCCACCCTCAAGTAGGCTCCAGTTTCTGTTGTTTCCTTCTTTGTGTCCATGAATTCTCATAAT T C PTCSC2 Ensembl:ENSG00000236130 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1020817001 Functional Loss SNV dbSNP153 33..33 33 - - - 47267 RMVar_ID_47267 Human_SNP_ID_408318284 A-to-I Human chr9 - 97884329 97884329 97884329 CACACTGACTAATGTTTAAAAATTGTAGAGACAGGATCTCACTATGTTGCTCAGGCTAGTCTTGA CACACTGACTAATGTTTAAAAATTGTAGAGACGGGATCTCACTATGTTGCTCAGGCTAGTCTTGA T C lnc-TRMO-2 RNACentral:URS00008BF48E lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1228008057 Functional Loss SNV dbSNP153 33..33 33 - - - 47268 RMVar_ID_47268 Human_SNP_ID_408322133 A-to-I Human chr9 - 97899562 97899562 97899562 AATTATAGAAATATTTTTTTAGGCTGGGCTCAAGAGGCTGAGGTGGGAGGATCATTTGACCTTGG AATTATAGAAATATTTTTTTAGGCTGGGCTCAGGAGGCTGAGGTGGGAGGATCATTTGACCTTGG T C lnc-TRMO-1 RNACentral:URS00008BFA22 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1231500702 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7880499,Human_RBP_ID_16519555,Human_RBP_ID_27780927 47269 RMVar_ID_47269 Human_SNP_ID_408322258 A-to-I Human chr9 - 97900038 97900038 97900038 TTTTGTTTTGTTTTTTGAGGCAGTCTTGCTCTATTGCCCAGGCTGGAGTGTAGTGGTGCAATCAC TTTTGTTTTGTTTTTTGAGGCAGTCTTGCTCTGTTGCCCAGGCTGGAGTGTAGTGGTGCAATCAC T C lnc-TRMO-1 RNACentral:URS00008BFA22 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1312107710 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7880501 47270 RMVar_ID_47270 Human_SNP_ID_408324313 A-to-I Human chr9 - 97908223 97908223 97908223 TATTTTTAGTAGAGACTGAGTTTCACCGTGTTAGGCAGGATGGTCTCGATCTCCTGACCTTGTGA TATTTTTAGTAGAGACTGAGTTTCACCGTGTTGGGCAGGATGGTCTCGATCTCCTGACCTTGTGA T C TRMO Ensembl:ENSG00000136932 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1395710758 Functional Loss SNV dbSNP153 33..33 33 - - - 47271 RMVar_ID_47271 Human_SNP_ID_408344717 A-to-I Human chr9 + 97988670 97988670 97988670 TTGCTTGAACCCCGGGGACAGAGTTTGCAGTGAGCCAAGATAACACCACTTCACTCCAGCATAGG TTGCTTGAACCCCGGGGACAGAGTTTGCAGTGCGCCAAGATAACACCACTTCACTCCAGCATAGG A C ANP32B Ensembl:ENSG00000136938 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1456485371 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16519957 47272 RMVar_ID_47272 Human_SNP_ID_408350860 A-to-I Human chr9 + 98013223 98013223 98013223 TTTTGTATTTTTAGTAGAGACAGGGTTTTGCCATGTTGGCCAGCCTGGTCTTGAATTCCTGGCTG TTTTGTATTTTTAGTAGAGACAGGGTTTTGCCGTGTTGGCCAGCCTGGTCTTGAATTCCTGGCTG A G ANP32B Ensembl:ENSG00000136938 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1215298552 Functional Loss SNV dbSNP153 33..33 33 - - - 47273 RMVar_ID_47273 Human_SNP_ID_408351020 A-to-I Human chr9 + 98013897 98013897 98013897 AAAAAGTTAGCTGCACATGGTGGTGCACACCTATAGTCCCAGCTACTTGGGAAGCTGAGGTGGGA AAAAAGTTAGCTGCACATGGTGGTGCACACCTGTAGTCCCAGCTACTTGGGAAGCTGAGGTGGGA A G ANP32B Ensembl:ENSG00000136938 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs978483992 Functional Loss SNV dbSNP153 33..33 33 - - - 47274 RMVar_ID_47274 Human_SNP_ID_408351277 A-to-I Human chr9 + 98014953 98014953 98014953 TTTTGTATTTTTAGTAGAGACGGAGTTTCACCATGTTGGCCAGGGTGGTCTGGAACTCCTGACCT TTTTGTATTTTTAGTAGAGACGGAGTTTCACCGTGTTGGCCAGGGTGGTCTGGAACTCCTGACCT A G ANP32B Ensembl:ENSG00000136938 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs569049168 Functional Loss SNV dbSNP153 33..33 33 - - - 47275 RMVar_ID_47275 Human_SNP_ID_408352359 A-to-I Human chr9 + 98018859 98018859 98018859 AGACGGTCTGACTCTGTCACCCAAGCTGGAATACACTGGCACAATCATGGTTCACTGCATGCTCG AGACGGTCTGACTCTGTCACCCAAGCTGGAATTCACTGGCACAATCATGGTTCACTGCATGCTCG A T L13712-001,lnc-ANP32B-1,RF00017-4531,lnc-ANP32B-1:2 RNACentral:URS0000334622,RNACentral:URS00009B29AC,RNACentral:URS000098F531,RNACentral:URS00008BF6B6 misc_RNA,lincRNA,SRP RNA,lincRNA intron,exon,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913050420 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_258161,RMVar_hsa_circ_86284 47276 RMVar_ID_47276 Human_SNP_ID_408354141 A-to-I Human chr9 + 98026450 98026450 98026450 CTGGCTCACAAGCAGCCTTTACCTCCAGGGTTAGGTGAGTCTCCCATCTCAGCCTCCCAAGCAGC CTGGCTCACAAGCAGCCTTTACCTCCAGGGTTTGGTGAGTCTCCCATCTCAGCCTCCCAAGCAGC A T L13712-001,RF00017-4531,lnc-ANP32B-1 RNACentral:URS0000334622,RNACentral:URS000098F531,RNACentral:URS00008BF6B6 misc_RNA,SRP RNA,lincRNA intron,intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs987597797 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_258161,RMVar_hsa_circ_86284 47277 RMVar_ID_47277 Human_SNP_ID_408354154 A-to-I Human chr9 + 98026490 98026490 98026490 CTCCCATCTCAGCCTCCCAAGCAGCTGAGACCACAAGCATGAGCTACCATGCCCAGCTCATTTTT CTCCCATCTCAGCCTCCCAAGCAGCTGAGACCGCAAGCATGAGCTACCATGCCCAGCTCATTTTT A G L13712-001,RF00017-4531,lnc-ANP32B-1 RNACentral:URS0000334622,RNACentral:URS000098F531,RNACentral:URS00008BF6B6 misc_RNA,SRP RNA,lincRNA intron,intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs551520927 Functional Loss SNV dbSNP153 33..33 33 - - - 47278 RMVar_ID_47278 Human_SNP_ID_408354155 A-to-I Human chr9 + 98026490 98026490 98026490 CTCCCATCTCAGCCTCCCAAGCAGCTGAGACCACAAGCATGAGCTACCATGCCCAGCTCATTTTT CTCCCATCTCAGCCTCCCAAGCAGCTGAGACCTCAAGCATGAGCTACCATGCCCAGCTCATTTTT A T L13712-001,RF00017-4531,lnc-ANP32B-1 RNACentral:URS0000334622,RNACentral:URS000098F531,RNACentral:URS00008BF6B6 misc_RNA,SRP RNA,lincRNA intron,intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs551520927 Functional Loss SNV dbSNP153 33..33 33 - - - 47279 RMVar_ID_47279 Human_SNP_ID_408354187 A-to-I Human chr9 + 98026626 98026626 98026626 CTCCCACCTCTGCCTCCCAAAGTGTTGCGATTAAAGGCGTGAGCCACCGTACCCAGACTCATCCA CTCCCACCTCTGCCTCCCAAAGTGTTGCGATTGAAGGCGTGAGCCACCGTACCCAGACTCATCCA A G L13712-001,RF00017-4531,lnc-ANP32B-1 RNACentral:URS0000334622,RNACentral:URS000098F531,RNACentral:URS00008BF6B6 misc_RNA,SRP RNA,lincRNA intron,intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs372196060 Functional Loss SNV dbSNP153 33..33 33 - - - 47280 RMVar_ID_47280 Human_SNP_ID_408354584 A-to-I Human chr9 + 98027752 98027751 98027753 ATTTTGTTTGTCTGTTTGTTTGTTTTTGAGACAGAGTCTCACTCTGTCATCCAGGCTGGAGTGCA ATTTTGTTTGTCTGTTTGTTTGTTTTTGAGAC__AGTCTCACTCTGTCATCCAGGCTGGAGTGCA CAG C L13712-001,RF00017-4531 RNACentral:URS0000334622,RNACentral:URS000098F531 misc_RNA,SRP RNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417153488 Functional Loss DEL dbSNP153 33..34 33 - - - 47281 RMVar_ID_47281 Human_SNP_ID_408354944 A-to-I Human chr9 + 98029468 98029468 98029468 AGCCTGGGCCACAAAGTAAGATCCCCATCTCTACAAAAAAAATTTAAAAATTAGCTGGGCATGGT AGCCTGGGCCACAAAGTAAGATCCCCATCTCTCCAAAAAAAATTTAAAAATTAGCTGGGCATGGT A C L13712-001,RF00017-4531 RNACentral:URS0000334622,RNACentral:URS000098F531 misc_RNA,SRP RNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1003001203 Functional Loss SNV dbSNP153 33..33 33 - - - 47282 RMVar_ID_47282 Human_SNP_ID_408368862 A-to-I Human chr9 - 98087414 98087414 98087414 TCCAGGTACGCCGCAGCTGCCCAGTCTCGCCTAATCTACCTAGATCAGCGTGGCTGGTCCCCTTA TCCAGGTACGCCGCAGCTGCCCAGTCTCGCCTTATCTACCTAGATCAGCGTGGCTGGTCCCCTTA T A TRIM14 Ensembl:ENSG00000106785 Protein coding intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1318717225 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1023573 RMVar_hsa_circ_85685,RMVar_hsa_circ_258168 47283 RMVar_ID_47283 Human_SNP_ID_408375075 A-to-I Human chr9 - 98112633 98112633 98112633 CACCACACCTGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCTCCATGTTGGTCAGGCTGG CACCACACCTGGCTAATTTTTGTATTTTTAGTGGAGACGGGGTTTCTCCATGTTGGTCAGGCTGG T C TRIM14 Ensembl:ENSG00000106785 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs951995630 Functional Loss SNV dbSNP153 33..33 33 - - - 47284 RMVar_ID_47284 Human_SNP_ID_408375087 A-to-I Human chr9 - 98112687 98112687 98112687 TTCAAGTGATCTCCTGCCTCAGCCTCCTGAGTAGCTGTGATTACAGGCGTGCACCACCACACCTG TTCAAGTGATCTCCTGCCTCAGCCTCCTGAGTGGCTGTGATTACAGGCGTGCACCACCACACCTG T C TRIM14 Ensembl:ENSG00000106785 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs751529807 Functional Loss SNV dbSNP153 33..33 33 - - - 47285 RMVar_ID_47285 Human_SNP_ID_408375193 A-to-I Human chr9 - 98113069 98113069 98113069 CGCTCTTGTTGCCCAGGCTGGAGTGCAGTGGCATGAACTGCCTCACTGCAACCTCCACCTCCCAG CGCTCTTGTTGCCCAGGCTGGAGTGCAGTGGCGTGAACTGCCTCACTGCAACCTCCACCTCCCAG T C TRIM14 Ensembl:ENSG00000106785 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs979557983 Functional Loss SNV dbSNP153 33..33 33 - - - 47286 RMVar_ID_47286 Human_SNP_ID_408375742 A-to-I Human chr9 - 98115415 98115415 98115415 TGAAACCTATCTCTACTAAGAATGCAAAAATTAGCTGGGCATGGTGGTGGGCACCTGTAATCCCA TGAAACCTATCTCTACTAAGAATGCAAAAATTTGCTGGGCATGGTGGTGGGCACCTGTAATCCCA T A TRIM14 Ensembl:ENSG00000106785 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1435227650 Functional Loss SNV dbSNP153 33..33 33 - - - 47287 RMVar_ID_47287 Human_SNP_ID_408375891 A-to-I Human chr9 - 98116065 98116065 98116065 AAAACTCCGACCTCAAGTGAACTGCCCACCTCAGTGTCCCAAAGTGCTGGGCCCCCTTTTATTGT AAAACTCCGACCTCAAGTGAACTGCCCACCTCCGTGTCCCAAAGTGCTGGGCCCCCTTTTATTGT T G TRIM14 Ensembl:ENSG00000106785 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs996840392 Functional Loss SNV dbSNP153 33..33 33 - - - 47288 RMVar_ID_47288 Human_SNP_ID_408376026 A-to-I Human chr9 - 98116671 98116671 98116671 CCTGGCTAATTTTTTTTTTGTATTTTTTTTGTAGAGACGGGGTTTCACCATGTTGTCCAGGCTGG CCTGGCTAATTTTTTTTTTGTATTTTTTTTGTGGAGACGGGGTTTCACCATGTTGTCCAGGCTGG T C TRIM14 Ensembl:ENSG00000106785 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs915805694 Functional Loss SNV dbSNP153 33..33 33 - - - 47289 RMVar_ID_47289 Human_SNP_ID_408376040 A-to-I Human chr9 - 98116722 98116722 98116722 CTCCTACCTTGGCCTCCCAAGTAGCTGGGACTATAGGTATGCACCACCACACCTGGCTAATTTTT CTCCTACCTTGGCCTCCCAAGTAGCTGGGACTGTAGGTATGCACCACCACACCTGGCTAATTTTT T C TRIM14 Ensembl:ENSG00000106785 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs190316726 Functional Loss SNV dbSNP153 33..33 33 - - - 47290 RMVar_ID_47290 Human_SNP_ID_408376306 A-to-I Human chr9 - 98117973 98117973 98117973 ATGGGGGACAATCCAGTGGAGTCGTGGGCTCAAGACCTGTCCCTGCCACCAGACCCTTCCTTTTT ATGGGGGACAATCCAGTGGAGTCGTGGGCTCAGGACCTGTCCCTGCCACCAGACCCTTCCTTTTT T C TRIM14 Ensembl:ENSG00000106785 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs956011110 Functional Loss SNV dbSNP153 33..33 33 - - - 47291 RMVar_ID_47291 Human_SNP_ID_408376386 A-to-I Human chr9 - 98118371 98118370 98118371 TTATTACAGCCATTTTATAGGCCACAAGAGGAAGGCTCTGGAGGCAGGGGCAGGCCTTGAACCCA TTATTACAGCCATTTTATAGGCCACAAGAGGA_GGCTCTGGAGGCAGGGGCAGGCCTTGAACCCA CT C TRIM14 Ensembl:ENSG00000106785 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1380931431 Functional Loss DEL dbSNP153 33..33 33 - - - 47292 RMVar_ID_47292 Human_SNP_ID_408396180 A-to-I Human chr9 - 98197608 98197608 98197608 CGGCTCACAACAACCTCTGACTCCCTGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCT CGGCTCACAACAACCTCTGACTCCCTGGTTCAGGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs999155114 Functional Loss SNV dbSNP153 33..33 33 - - - 47293 RMVar_ID_47293 Human_SNP_ID_408407230 A-to-I Human chr9 - 98243052 98243052 98243052 GTATGGACCAGGCGTCGTGGTTCATGCCTGTAATTGCAACACTTTGGGAGGCCAAGACAGGAGGA GTATGGACCAGGCGTCGTGGTTCATGCCTGTAGTTGCAACACTTTGGGAGGCCAAGACAGGAGGA T C TBC1D2 Ensembl:ENSG00000095383 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs889160970 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7861,RMVar_hsa_circ_50695 47294 RMVar_ID_47294 Human_SNP_ID_408494172 A-to-I Human chr9 + 98607941 98607941 98607941 ATGAAGGTCAAAGAAAAAGTTCAAAACTGAAGAACTCTGAAGCTGAGCTCCAGCGGCACCATGAG ATGAAGGTCAAAGAAAAAGTTCAAAACTGAAGGACTCTGAAGCTGAGCTCCAGCGGCACCATGAG A G SEPTIN7P7 Ensembl:ENSG00000229897 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1397022118 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18542156,Human_RBP_ID_26559423 47295 RMVar_ID_47295 Human_SNP_ID_408578410 A-to-I Human chr9 + 98959071 98959071 98959071 CATGGAATGGCTGAGAAATTTTTCATACCTGGAAAGAGTATTGTAGCTTTGTTTTAAAGAAATTA CATGGAATGGCTGAGAAATTTTTCATACCTGGGAAGAGTATTGTAGCTTTGTTTTAAAGAAATTA A G COL15A1 Ensembl:ENSG00000204291 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs767111310 Functional Loss SNV dbSNP153 33..33 33 - - - 47296 RMVar_ID_47296 Human_SNP_ID_408603694 A-to-I Human chr9 + 99060704 99060704 99060704 GTCTAGGAGTTCAAGACTAGCCTGGGCAACATAGTGAGATCCTGCCTCTACAGAAAAATGTAAAA GTCTAGGAGTTCAAGACTAGCCTGGGCAACATGGTGAGATCCTGCCTCTACAGAAAAATGTAAAA A G COL15A1 Ensembl:ENSG00000204291 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1564094048 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15054,RMVar_hsa_circ_70821,RMVar_hsa_circ_258215 47297 RMVar_ID_47297 Human_SNP_ID_408799243 A-to-I Human chr9 + 99911642 99911642 99911642 ATCTCACTGTGTTGCCTAGGCTGTAGTGTAGTAGTAAGAACACTGTTTCTTGCAGGCTCACACTT ATCTCACTGTGTTGCCTAGGCTGTAGTGTAGTGGTAAGAACACTGTTTCTTGCAGGCTCACACTT A G STX17 Ensembl:ENSG00000136874 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1291736560 Functional Loss SNV dbSNP153 33..33 33 - - - 47298 RMVar_ID_47298 Human_SNP_ID_408809869 A-to-I Human chr9 + 99959314 99959314 99959314 CCTGTAATTCTAGCATTTTGGGAAGCTGAGGCAGGAGGATCAGTTGAGGCCGGGAGTTCAAGACC CCTGTAATTCTAGCATTTTGGGAAGCTGAGGCTGGAGGATCAGTTGAGGCCGGGAGTTCAAGACC A T STX17 Ensembl:ENSG00000136874 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1554702559 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4956,RMVar_hsa_circ_62704 47299 RMVar_ID_47299 Human_SNP_ID_408809870 A-to-I Human chr9 + 99959317 99959317 99959317 GTAATTCTAGCATTTTGGGAAGCTGAGGCAGGAGGATCAGTTGAGGCCGGGAGTTCAAGACCAGC GTAATTCTAGCATTTTGGGAAGCTGAGGCAGGGGGATCAGTTGAGGCCGGGAGTTCAAGACCAGC A G STX17 Ensembl:ENSG00000136874 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs142014177 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4956,RMVar_hsa_circ_62704 47300 RMVar_ID_47300 Human_SNP_ID_408817954 A-to-I Human chr9 - 99995802 99995802 99995802 TATGTTCATTGCAGCATTATTCACAATAGGCAAGATACGGAATCAATCCAAGTGTCTGTCTACAG TATGTTCATTGCAGCATTATTCACAATAGGCAGGATACGGAATCAATCCAAGTGTCTGTCTACAG T C ERP44 Ensembl:ENSG00000023318 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1009054756 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120989,RMVar_hsa_circ_45564,RMVar_hsa_circ_258248,RMVar_hsa_circ_349424,RMVar_hsa_circ_50537 47301 RMVar_ID_47301 Human_SNP_ID_408817955 A-to-I Human chr9 - 99995807 99995807 99995807 ACTCCTATGTTCATTGCAGCATTATTCACAATAGGCAAGATACGGAATCAATCCAAGTGTCTGTC ACTCCTATGTTCATTGCAGCATTATTCACAATCGGCAAGATACGGAATCAATCCAAGTGTCTGTC T G ERP44 Ensembl:ENSG00000023318 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs891722417 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120989,RMVar_hsa_circ_45564,RMVar_hsa_circ_258248,RMVar_hsa_circ_349424,RMVar_hsa_circ_50537 47302 RMVar_ID_47302 Human_SNP_ID_408830285 A-to-I Human chr9 - 100052522 100052522 100052522 TGGCATCCTTCTCTGTGTATAGGTGTCGTTTCAGTCAGATGTTGCATCCAATTTTTGAGGAAGCT TGGCATCCTTCTCTGTGTATAGGTGTCGTTTCGGTCAGATGTTGCATCCAATTTTTGAGGAAGCT T C ERP44 Ensembl:ENSG00000023318 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1184949450 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9338993,Human_RBP_ID_17322973,Human_RBP_ID_17666324,Human_RBP_ID_22467361,Human_RBP_ID_22776510 Human_Splice_Rec_1067746 RMVar_hsa_circ_33320,RMVar_hsa_circ_45564,RMVar_hsa_circ_74445,RMVar_hsa_circ_327441,RMVar_hsa_circ_52639,RMVar_hsa_circ_258254,RMVar_hsa_circ_258256,RMVar_hsa_circ_86285,RMVar_hsa_circ_258257,RMVar_hsa_circ_275152 47303 RMVar_ID_47303 Human_SNP_ID_408831466 A-to-I Human chr9 - 100058214 100058214 100058214 AAAATTAGCCAGGTGTGGTGGTGTTTGCCTGTAGTCCTAGCTACTTGGGAGGGTGAAGTGGGAGG AAAATTAGCCAGGTGTGGTGGTGTTTGCCTGTGGTCCTAGCTACTTGGGAGGGTGAAGTGGGAGG T C ERP44 Ensembl:ENSG00000023318 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1477316187 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74445,RMVar_hsa_circ_258256,RMVar_hsa_circ_86285,RMVar_hsa_circ_258257,RMVar_hsa_circ_275152 47304 RMVar_ID_47304 Human_SNP_ID_408831734 A-to-I Human chr9 - 100059503 100059503 100059503 TTAAATTTTTCTTGTAGAGACATGGTCTTGCTATGTTGCCCAGGCTGGTCTTGAATTCCTGACCT TTAAATTTTTCTTGTAGAGACATGGTCTTGCTGTGTTGCCCAGGCTGGTCTTGAATTCCTGACCT T C ERP44 Ensembl:ENSG00000023318 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs745505325 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74445,RMVar_hsa_circ_258256,RMVar_hsa_circ_86285,RMVar_hsa_circ_258257,RMVar_hsa_circ_275152 47305 RMVar_ID_47305 Human_SNP_ID_408831735 A-to-I Human chr9 - 100059503 100059503 100059503 TTAAATTTTTCTTGTAGAGACATGGTCTTGCTATGTTGCCCAGGCTGGTCTTGAATTCCTGACCT TTAAATTTTTCTTGTAGAGACATGGTCTTGCTCTGTTGCCCAGGCTGGTCTTGAATTCCTGACCT T G ERP44 Ensembl:ENSG00000023318 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs745505325 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74445,RMVar_hsa_circ_258256,RMVar_hsa_circ_86285,RMVar_hsa_circ_258257,RMVar_hsa_circ_275152 47306 RMVar_ID_47306 Human_SNP_ID_408835132 A-to-I Human chr9 - 100071869 100071869 100071869 TTGCCCAGGCTAGAGTGCAATGGCGTGATCTCAGCTCACAGCAACTTCCACCTCCCGGGTTAAAG TTGCCCAGGCTAGAGTGCAATGGCGTGATCTCGGCTCACAGCAACTTCCACCTCCCGGGTTAAAG T C ERP44 Ensembl:ENSG00000023318 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs925683686 Functional Loss SNV dbSNP153 33..33 33 - - - 47307 RMVar_ID_47307 Human_SNP_ID_408842785 A-to-I Human chr9 + 100102201 100102201 100102201 CTGCAACCTCCATCCACCTCCCAAATTCAAGCAATTCTCCCACCTCAGCCTCCTGAGTAGCTAGG CTGCAACCTCCATCCACCTCCCAAATTCAAGCGATTCTCCCACCTCAGCCTCCTGAGTAGCTAGG A G INVS Ensembl:ENSG00000119509 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1447367168 Functional Loss SNV dbSNP153 33..33 33 - - - 47308 RMVar_ID_47308 Human_SNP_ID_408842786 A-to-I Human chr9 + 100102210 100102210 100102210 CCATCCACCTCCCAAATTCAAGCAATTCTCCCACCTCAGCCTCCTGAGTAGCTAGGATTACAGGT CCATCCACCTCCCAAATTCAAGCAATTCTCCCCCCTCAGCCTCCTGAGTAGCTAGGATTACAGGT A C INVS Ensembl:ENSG00000119509 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1048813745 Functional Loss SNV dbSNP153 33..33 33 - - - 47309 RMVar_ID_47309 Human_SNP_ID_408843096 A-to-I Human chr9 + 100103407 100103406 100103407 CCAGCACTTTGGGATGCCAAGGTGGGCAGATCACTTGAGATCAGGAGTTCGAGACCAGCCTGGCC CCAGCACTTTGGGATGCCAAGGTGGGCAGATC_CTTGAGATCAGGAGTTCGAGACCAGCCTGGCC CA C INVS Ensembl:ENSG00000119509 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1297976336 Functional Loss DEL dbSNP153 33..33 33 - - - 47310 RMVar_ID_47310 Human_SNP_ID_408843101 A-to-I Human chr9 + 100103417 100103417 100103417 GGGATGCCAAGGTGGGCAGATCACTTGAGATCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGA GGGATGCCAAGGTGGGCAGATCACTTGAGATCTGGAGTTCGAGACCAGCCTGGCCAACATGGTGA A T INVS Ensembl:ENSG00000119509 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1461110724 Functional Loss SNV dbSNP153 33..33 33 - - - 47311 RMVar_ID_47311 Human_SNP_ID_408843136 A-to-I Human chr9 + 100103505 100103505 100103505 CAAAACTTAGCCGGTCGTGATGGCAGGTGCCTATAATCCCAGCTACTGAGGAGGCTGAGGCAGGA CAAAACTTAGCCGGTCGTGATGGCAGGTGCCTGTAATCCCAGCTACTGAGGAGGCTGAGGCAGGA A G INVS Ensembl:ENSG00000119509 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1262619424 Functional Loss SNV dbSNP153 33..33 33 - - - 47312 RMVar_ID_47312 Human_SNP_ID_408843138 A-to-I Human chr9 + 100103513 100103513 100103513 AGCCGGTCGTGATGGCAGGTGCCTATAATCCCAGCTACTGAGGAGGCTGAGGCAGGAGACTTGCT AGCCGGTCGTGATGGCAGGTGCCTATAATCCCTGCTACTGAGGAGGCTGAGGCAGGAGACTTGCT A T INVS Ensembl:ENSG00000119509 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1453434042 Functional Loss SNV dbSNP153 33..33 33 - - - 47313 RMVar_ID_47313 Human_SNP_ID_408843148 A-to-I Human chr9 + 100103569 100103569 100103569 AGACTTGCTTGAGCCCTGGAGGCAGAGGCTGCAATGAGCTGACATCGCACCACTGCACTCTAGCC AGACTTGCTTGAGCCCTGGAGGCAGAGGCTGCGATGAGCTGACATCGCACCACTGCACTCTAGCC A G INVS Ensembl:ENSG00000119509 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1185729094 Functional Loss SNV dbSNP153 33..33 33 - - - 47314 RMVar_ID_47314 Human_SNP_ID_408865862 A-to-I Human chr9 + 100203703 100203703 100203703 TTTTGTATTTTTAGTAGAGACAGGTTTTTACCATGTTGGCCAGATTGGTCTCGAACTCCTGACCT TTTTGTATTTTTAGTAGAGACAGGTTTTTACCGTGTTGGCCAGATTGGTCTCGAACTCCTGACCT A G INVS Ensembl:ENSG00000119509 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1050281485 Functional Loss SNV dbSNP153 33..33 33 - - - 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 47315 RMVar_ID_47315 Human_SNP_ID_408893902 A-to-I Human chr9 - 100325515 100325515 100325515 AAAAAAAGAAAGTTTTAATATTTCAAGAGACAAGTTCTCACTCTGTTGCCCAGATTAGAGTGCAA AAAAAAAGAAAGTTTTAATATTTCAAGAGACAGGTTCTCACTCTGTTGCCCAGATTAGAGTGCAA T C TEX10 Ensembl:ENSG00000136891 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1469167063 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17579325 RMVar_hsa_circ_337719,RMVar_hsa_circ_338094,RMVar_hsa_circ_279197,RMVar_hsa_circ_258283,RMVar_hsa_circ_258284,RMVar_hsa_circ_258285,RMVar_hsa_circ_334852,RMVar_hsa_circ_338764,RMVar_hsa_circ_345717,RMVar_hsa_circ_111832,RMVar_hsa_circ_74721,RMVar_hsa_circ_9322,RMVar_hsa_circ_258286,RMVar_hsa_circ_258287,RMVar_hsa_circ_327595,RMVar_hsa_circ_33813,RMVar_hsa_circ_330937,RMVar_hsa_circ_264969,RMVar_hsa_circ_365810,RMVar_hsa_circ_369759,RMVar_hsa_circ_279003,RMVar_hsa_circ_279623,RMVar_hsa_circ_258293,RMVar_hsa_circ_258295,RMVar_hsa_circ_258296,RMVar_hsa_circ_258294,RMVar_hsa_circ_258292,RMVar_hsa_circ_5280,RMVar_hsa_circ_91722,RMVar_hsa_circ_351476,RMVar_hsa_circ_258297,RMVar_hsa_circ_258298 47316 RMVar_ID_47316 Human_SNP_ID_408895634 A-to-I Human chr9 - 100332721 100332721 100332721 CACCTCCCGGGTTCACGCTATTCTCCTGGCTCAGCCTCCTGAGTAGCTGGGACTACAGGTGCCTG CACCTCCCGGGTTCACGCTATTCTCCTGGCTCGGCCTCCTGAGTAGCTGGGACTACAGGTGCCTG T C TEX10 Ensembl:ENSG00000136891 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1415312270 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_338094,RMVar_hsa_circ_279197,RMVar_hsa_circ_258284,RMVar_hsa_circ_258285,RMVar_hsa_circ_334852,RMVar_hsa_circ_345717,RMVar_hsa_circ_74721,RMVar_hsa_circ_44334,RMVar_hsa_circ_327595,RMVar_hsa_circ_330937,RMVar_hsa_circ_264969,RMVar_hsa_circ_365810,RMVar_hsa_circ_279623,RMVar_hsa_circ_258295,RMVar_hsa_circ_258296,RMVar_hsa_circ_5280,RMVar_hsa_circ_20446,RMVar_hsa_circ_56013,RMVar_hsa_circ_30804,RMVar_hsa_circ_69616,RMVar_hsa_circ_68883 47317 RMVar_ID_47317 Human_SNP_ID_408911784 A-to-I Human chr9 + 100398628 100398628 100398628 TCCCCTAGGCTGGAGTGCAGTGGTGTAATCTCAGCTCACTGCAGCCTCCACCTCCCAGGCTCAAG TCCCCTAGGCTGGAGTGCAGTGGTGTAATCTCGGCTCACTGCAGCCTCCACCTCCCAGGCTCAAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1489219158 Functional Loss SNV dbSNP153 33..33 33 - - - 47318 RMVar_ID_47318 Human_SNP_ID_408924650 A-to-I Human chr9 + 100452663 100452663 100452663 GCCTCGGCCTCCCAAAGTGCTGGATTACAGGCATGAGCCACCGCGCCCGGCTGGTCTGTATAGCC GCCTCGGCCTCCCAAAGTGCTGGATTACAGGCGTGAGCCACCGCGCCCGGCTGGTCTGTATAGCC A G MSANTD3-TMEFF1 Ensembl:ENSG00000251349 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs981943019 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_258305,RMVar_hsa_circ_258304 47319 RMVar_ID_47319 Human_SNP_ID_408925116 A-to-I Human chr9 + 100454728 100454723 100454729 ATGGTGAAACCCCGTCTATACTAAAAATACAAAAAGATAGCCAGACGTGGTGGCAGGCGCCTGTA ATGGTGAAACCCCGTCTATACTAAAAAT______AGATAGCCAGACGTGGTGGCAGGCGCCTGTA TACAAAA T MSANTD3-TMEFF1 Ensembl:ENSG00000251349 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232705786 Functional Loss DEL dbSNP153 29..34 33 - - - RMVar_hsa_circ_258305,RMVar_hsa_circ_258304 47320 RMVar_ID_47320 Human_SNP_ID_408925120 A-to-I Human chr9 + 100454728 100454728 100454728 ATGGTGAAACCCCGTCTATACTAAAAATACAAAAAGATAGCCAGACGTGGTGGCAGGCGCCTGTA ATGGTGAAACCCCGTCTATACTAAAAATACAACAAGATAGCCAGACGTGGTGGCAGGCGCCTGTA A C MSANTD3-TMEFF1 Ensembl:ENSG00000251349 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1272646011 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_258305,RMVar_hsa_circ_258304 47321 RMVar_ID_47321 Human_SNP_ID_408939223 A-to-I Human chr9 + 100515711 100515711 100515711 AGGAGGCTGAGGCAGGAGAATCACTTGAACCCAGGAGGCAGAGGTTCAAGTGATTCTCCAGGCTG AGGAGGCTGAGGCAGGAGAATCACTTGAACCCGGGAGGCAGAGGTTCAAGTGATTCTCCAGGCTG A G TMEFF1,MSANTD3-TMEFF1 Ensembl:ENSG00000241697,Ensembl:ENSG00000251349 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1162993604 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_258312,RMVar_hsa_circ_258305,RMVar_hsa_circ_271890,RMVar_hsa_circ_278274,RMVar_hsa_circ_324048,RMVar_hsa_circ_273805,RMVar_hsa_circ_258314,RMVar_hsa_circ_258315,RMVar_hsa_circ_258313,RMVar_hsa_circ_258308,RMVar_hsa_circ_258310,RMVar_hsa_circ_258311,RMVar_hsa_circ_258309,RMVar_hsa_circ_45440,RMVar_hsa_circ_20768,RMVar_hsa_circ_310606,RMVar_hsa_circ_258307,RMVar_hsa_circ_291153,RMVar_hsa_circ_258318,RMVar_hsa_circ_258319 47322 RMVar_ID_47322 Human_SNP_ID_409151072 A-to-I Human chr9 - 101390418 101390418 101390418 AACACATTGAAATCACTGTCTTTCCCTGAGCAAGGGGGCTGCTCATTAGATCTTTTGATACTTTA AACACATTGAAATCACTGTCTTTCCCTGAGCATGGGGGCTGCTCATTAGATCTTTTGATACTTTA T A MRPL50 Ensembl:ENSG00000136897 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1000373237 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_707851,Human_RBP_ID_797458,Human_RBP_ID_5154821,Human_RBP_ID_7882847,Human_RBP_ID_16527935,Human_RBP_ID_17323580,Human_RBP_ID_17547561,Human_RBP_ID_18394237,Human_RBP_ID_22119854 RMVar_hsa_circ_92991,RMVar_hsa_circ_101206,RMVar_hsa_circ_258334,RMVar_hsa_circ_258335 47323 RMVar_ID_47323 Human_SNP_ID_409195400 A-to-I Human chr9 + 101565047 101565047 101565047 CAGCCCAGGCAACATAGGGAGACCCCGTCTCTACAAAAAATTTCGAAAATTAGCTGGCTGTGGTG CAGCCCAGGCAACATAGGGAGACCCCGTCTCTGCAAAAAATTTCGAAAATTAGCTGGCTGTGGTG A G - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1156620554 Functional Loss SNV dbSNP153 33..33 33 - - - 47324 RMVar_ID_47324 Human_SNP_ID_409195442 A-to-I Human chr9 + 101565168 101565168 101565168 ACCGGAGGTTAAGGCTGCTGTGAGCTGTGATTATGCCATGGACTCCAGCCTGGGTGACACAGTGA ACCGGAGGTTAAGGCTGCTGTGAGCTGTGATTGTGCCATGGACTCCAGCCTGGGTGACACAGTGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1280177401 Functional Loss SNV dbSNP153 33..33 33 - - - 47325 RMVar_ID_47325 Human_SNP_ID_409423354 A-to-I Human chr9 - 102441549 102441549 102441549 ATTCTCTAGCTTTGACTTTTTGGACTGTTATTACTTTCTTTCACTATTTACAAAGCCCCTCTCCA ATTCTCTAGCTTTGACTTTTTGGACTGTTATTTCTTTCTTTCACTATTTACAAAGCCCCTCTCCA T A lnc-GRIN3A-6,lnc-GRIN3A-4 RNACentral:URS0000D5D8A5,RNACentral:URS00008B3A8A lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1271386104 Functional Loss SNV dbSNP153 33..33 33 - - - 47326 RMVar_ID_47326 Human_SNP_ID_409866496 A-to-I Human chr9 - 104140063 104140063 104140063 ATATTAACAAACTTCAGATAAATTTGCAGCAGATAGTACCACGCAACACACCTCCTAAGCTTTGA ATATTAACAAACTTCAGATAAATTTGCAGCAGCTAGTACCACGCAACACACCTCCTAAGCTTTGA T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1265041774 Functional Loss SNV dbSNP153 33..33 33 - - - 47327 RMVar_ID_47327 Human_SNP_ID_410017416 A-to-I Human chr9 + 104756903 104756903 104756903 TCAGCTCCCTGCAACCTCCGCCTCCTTGGTTCAGGCGGTTCTCCTGCCTCAGCCTCCCAAGTAGC TCAGCTCCCTGCAACCTCCGCCTCCTTGGTTCGGGCGGTTCTCCTGCCTCAGCCTCCCAAGTAGC A G NIPSNAP3A Ensembl:ENSG00000136783 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1024161826 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127568,RMVar_hsa_circ_299051,RMVar_hsa_circ_378492,RMVar_hsa_circ_258360,RMVar_hsa_circ_258362,RMVar_hsa_circ_258363,RMVar_hsa_circ_258361,RMVar_hsa_circ_104452,RMVar_hsa_circ_258365,RMVar_hsa_circ_258364 47328 RMVar_ID_47328 Human_SNP_ID_410017424 A-to-I Human chr9 + 104756921 104756921 104756921 CGCCTCCTTGGTTCAGGCGGTTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGCTGTGTG CGCCTCCTTGGTTCAGGCGGTTCTCCTGCCTCGGCCTCCCAAGTAGCTGGGATTACAGCTGTGTG A G NIPSNAP3A Ensembl:ENSG00000136783 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1268726183 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127568,RMVar_hsa_circ_299051,RMVar_hsa_circ_378492,RMVar_hsa_circ_258360,RMVar_hsa_circ_258362,RMVar_hsa_circ_258363,RMVar_hsa_circ_258361,RMVar_hsa_circ_104452,RMVar_hsa_circ_258365,RMVar_hsa_circ_258364 47329 RMVar_ID_47329 Human_SNP_ID_529060930 A-to-I Human chr13 + 45030433 45030433 45030433 ATGGAGTCTTGCTCTGTCACCCAGGCTGGAGTAGAGTGGCGTGATCTCAGCTTACTGCAACCTCC ATGGAGTCTTGCTCTGTCACCCAGGCTGGAGTGGAGTGGCGTGATCTCAGCTTACTGCAACCTCC A G GPALPP1 Ensembl:ENSG00000133114 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1418821327 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_163159,RMVar_hsa_circ_102261,RMVar_hsa_circ_163164,RMVar_hsa_circ_99909,RMVar_hsa_circ_163166,RMVar_hsa_circ_80478,RMVar_hsa_circ_163167 47330 RMVar_ID_47330 Human_SNP_ID_529060986 A-to-I Human chr13 + 45030645 45030645 45030645 ACCTCAGGTGATCTACCTGCCTCGGCCTCCCAAAATGCTGGGATTACAGGCATCAGCCACCATGC ACCTCAGGTGATCTACCTGCCTCGGCCTCCCAGAATGCTGGGATTACAGGCATCAGCCACCATGC A G GPALPP1 Ensembl:ENSG00000133114 Protein coding 3'UTR GSE38233;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;esophageal squamous carcinoma cells,EC109 cell line - 24183664,32596459 RNA-Seq:(High) rs1280581942 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26425537 RMVar_hsa_circ_163159 47331 RMVar_ID_47331 Human_SNP_ID_529061022 A-to-I Human chr13 + 45030894 45030894 45030894 AAAAGATGAATTAGCTGGGCGCAGTGGCTCATACCTATAATCCCAGCACTTTGGGAGGCCGAGGT AAAAGATGAATTAGCTGGGCGCAGTGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCCGAGGT A G GPALPP1 Ensembl:ENSG00000133114 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs997971608 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_163159 47332 RMVar_ID_47332 Human_SNP_ID_529061023 A-to-I Human chr13 + 45030898 45030898 45030898 GATGAATTAGCTGGGCGCAGTGGCTCATACCTATAATCCCAGCACTTTGGGAGGCCGAGGTGGGT GATGAATTAGCTGGGCGCAGTGGCTCATACCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGT A G GPALPP1 Ensembl:ENSG00000133114 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs910697220 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_163159 47333 RMVar_ID_47333 Human_SNP_ID_529061053 A-to-I Human chr13 + 45031049 45031049 45031049 CTGGTGGCGGGTGCCTGTAATCCCAGCTACTCAGGAGGCTGAAGCAGGATAATTGCTTGAACCTA CTGGTGGCGGGTGCCTGTAATCCCAGCTACTCGGGAGGCTGAAGCAGGATAATTGCTTGAACCTA A G GPALPP1 Ensembl:ENSG00000133114 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1042385243 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_163159 47334 RMVar_ID_47334 Human_SNP_ID_529061070 A-to-I Human chr13 + 45031105 45031105 45031105 TTGAACCTAGGAGGCGGAGGTTGCAGTGAGCCAAGATCACACCATTGCATTCCAGCCTGGGCAAC TTGAACCTAGGAGGCGGAGGTTGCAGTGAGCCGAGATCACACCATTGCATTCCAGCCTGGGCAAC A G GPALPP1 Ensembl:ENSG00000133114 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs904320532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26425538 RMVar_hsa_circ_163159 47335 RMVar_ID_47335 Human_SNP_ID_529061409 A-to-I Human chr13 + 45032780 45032780 45032780 GAGATTGGCCAGGTGCGGTGGCTCACGCCTGTAATTCTAGCACTTTGGGAGGCCAAGGCAGGCGG GAGATTGGCCAGGTGCGGTGGCTCACGCCTGTGATTCTAGCACTTTGGGAGGCCAAGGCAGGCGG A G GPALPP1 Ensembl:ENSG00000133114 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1226946418 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_163159 47336 RMVar_ID_47336 Human_SNP_ID_529092725 A-to-I Human chr13 + 45164461 45164460 45164462 AAGTAAAGAAGTAGCAGCCCTAGTGGCCAGGTAGTGGCTCATGCCTGTAACCCCAGCACTTTGGG AAGTAAAGAAGTAGCAGCCCTAGTGGCCAGGT__TGGCTCATGCCTGTAACCCCAGCACTTTGGG TAG T GTF2F2 Ensembl:ENSG00000188342 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1243656623 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_33298,RMVar_hsa_circ_312442,RMVar_hsa_circ_277418,RMVar_hsa_circ_163171,RMVar_hsa_circ_163172 47337 RMVar_ID_47337 Human_SNP_ID_529134990 A-to-I Human chr13 - 45331993 45331993 45331993 GTCAGAGCACTTGAGCTCAGGAGTTTGAGACCAGTCTGGACAACATGGTGAAAGCCCATCTCTAT GTCAGAGCACTTGAGCTCAGGAGTTTGAGACCGGTCTGGACAACATGGTGAAAGCCCATCTCTAT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041714740 Functional Loss SNV dbSNP153 33..33 33 - - - 47338 RMVar_ID_47338 Human_SNP_ID_529134991 A-to-I Human chr13 - 45331993 45331993 45331993 GTCAGAGCACTTGAGCTCAGGAGTTTGAGACCAGTCTGGACAACATGGTGAAAGCCCATCTCTAT GTCAGAGCACTTGAGCTCAGGAGTTTGAGACCCGTCTGGACAACATGGTGAAAGCCCATCTCTAT T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041714740 Functional Loss SNV dbSNP153 33..33 33 - - - 47339 RMVar_ID_47339 Human_SNP_ID_529135043 A-to-I Human chr13 - 45332183 45332183 45332183 GGAAGTCAGGGTCTTGCTATGTTGCTGGAACTAATCTCAAACTCCTGGCCTCAAGTGATCCTCCT GGAAGTCAGGGTCTTGCTATGTTGCTGGAACTGATCTCAAACTCCTGGCCTCAAGTGATCCTCCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1012069128 Functional Loss SNV dbSNP153 33..33 33 - - - 47340 RMVar_ID_47340 Human_SNP_ID_529135590 A-to-I Human chr13 - 45334095 45334095 45334095 CCAGCCTGGGCAACATAGGGAGACCTAAAAAAATTAATTGGGCATCTGTAGTCCCAGCTACTCAG CCAGCCTGGGCAACATAGGGAGACCTAAAAAACTTAATTGGGCATCTGTAGTCCCAGCTACTCAG T G TPT1 Ensembl:ENSG00000133112 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1218521830 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9754275,Human_RBP_ID_12166323,Human_RBP_ID_17562003,Human_RBP_ID_22920428,Human_RBP_ID_25052417 47341 RMVar_ID_47341 Human_SNP_ID_529136240 A-to-I Human chr13 - 45336149 45336149 45336149 GGACTGCAGGCATGCACCCCTATGCCCAGCTAATTTTTGTAGAGACCGAGTATCGCTTAGTTGCC GGACTGCAGGCATGCACCCCTATGCCCAGCTAGTTTTTGTAGAGACCGAGTATCGCTTAGTTGCC T C TPT1 Ensembl:ENSG00000133112 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs937697322 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12166415 47342 RMVar_ID_47342 Human_SNP_ID_529136256 A-to-I Human chr13 - 45336198 45336198 45336198 TGCATCCTGTGCTCAAGCCATTTTCCCACCTCAGTCTCACTAGTTGCTGGGACTGCAGGCATGCA TGCATCCTGTGCTCAAGCCATTTTCCCACCTCGGTCTCACTAGTTGCTGGGACTGCAGGCATGCA T C TPT1 Ensembl:ENSG00000133112 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs766142151 Functional Loss SNV dbSNP153 33..33 33 - - - 47343 RMVar_ID_47343 Human_SNP_ID_529136265 A-to-I Human chr13 - 45336216 45336216 45336216 GCAACTCACTGCATTCTCTGCATCCTGTGCTCAAGCCATTTTCCCACCTCAGTCTCACTAGTTGC GCAACTCACTGCATTCTCTGCATCCTGTGCTCGAGCCATTTTCCCACCTCAGTCTCACTAGTTGC T C TPT1 Ensembl:ENSG00000133112 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs914894941 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6286150 47344 RMVar_ID_47344 Human_SNP_ID_529136266 A-to-I Human chr13 - 45336216 45336216 45336216 GCAACTCACTGCATTCTCTGCATCCTGTGCTCAAGCCATTTTCCCACCTCAGTCTCACTAGTTGC GCAACTCACTGCATTCTCTGCATCCTGTGCTCCAGCCATTTTCCCACCTCAGTCTCACTAGTTGC T G TPT1 Ensembl:ENSG00000133112 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs914894941 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6286150 47345 RMVar_ID_47345 Human_SNP_ID_529136275 A-to-I Human chr13 - 45336245 45336245 45336245 TCACCCAGGCTTGTAGTGCAGTGGCACAAGCAACTCACTGCATTCTCTGCATCCTGTGCTCAAGC TCACCCAGGCTTGTAGTGCAGTGGCACAAGCAGCTCACTGCATTCTCTGCATCCTGTGCTCAAGC T C TPT1 Ensembl:ENSG00000133112 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs796112444 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1272500,Human_RBP_ID_1809602,Human_RBP_ID_6286151,Human_RBP_ID_9754294,Human_RBP_ID_12166421,Human_RBP_ID_18268814,Human_RBP_ID_22920435 47346 RMVar_ID_47346 Human_SNP_ID_529137597 A-to-I Human chr13 - 45340037 45340037 45340037 TCATGAACCATCACCTGCAGGAAACAAGTTTCACAAAAGAAGCCTACAAGAAGTACATCAAAGAT TCATGAACCATCACCTGCAGGAAACAAGTTTCCCAAAAGAAGCCTACAAGAAGTACATCAAAGAT T G TPT1 Ensembl:ENSG00000133112 Protein coding CDS GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs373889573 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_880133,Human_RBP_ID_1809626,Human_RBP_ID_2384182,Human_RBP_ID_8392600,Human_RBP_ID_9032130,Human_RBP_ID_17245733,Human_RBP_ID_17476763,Human_RBP_ID_18527742,Human_RBP_ID_21886200,Human_RBP_ID_26807738,Human_RBP_ID_26916331 Human_Splice_Rec_1461199,Human_Splice_Rec_1461209,Human_Splice_Rec_1461217,Human_Splice_Rec_1461231,Human_Splice_Rec_1461241,Human_Splice_Rec_1461257,Human_Splice_Rec_1461265,Human_Splice_Rec_1461275,Human_Splice_Rec_1461283 RMVar_hsa_circ_103801,RMVar_hsa_circ_121231,RMVar_hsa_circ_163176,RMVar_hsa_circ_163175,RMVar_hsa_circ_365519,RMVar_hsa_circ_60043,RMVar_hsa_circ_61703,RMVar_hsa_circ_371705,RMVar_hsa_circ_163182 47347 RMVar_ID_47347 Human_SNP_ID_529139238 A-to-I Human chr13 + 45343772 45343772 45343772 GCCTTTGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGTGG GCCTTTGGCCGGGCGCGGTGGCTCACGCCTGTCATCCCAGCACTTTGGGAGGCCGAGGCAGGTGG A C TPT1-AS1 Ensembl:ENSG00000170919 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1299933873 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126449,RMVar_hsa_circ_163183 47348 RMVar_ID_47348 Human_SNP_ID_529139421 A-to-I Human chr13 + 45344345 45344345 45344345 TCGCTGTGTTGTCCAGGCTGGAGTGCAGTGGCACCATCTCGGCTCACTGCAACCTCTGGCTCCCA TCGCTGTGTTGTCCAGGCTGGAGTGCAGTGGCGCCATCTCGGCTCACTGCAACCTCTGGCTCCCA A G TPT1-AS1 Ensembl:ENSG00000170919 lincRNA intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1041751267 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4277031 Human_Splice_Rec_1461416,Human_Splice_Rec_1461444,Human_Splice_Rec_1461452,Human_Splice_Rec_1461488,Human_Splice_Rec_1461598,Human_Splice_Rec_1461616,Human_Splice_Rec_1461620,Human_Splice_Rec_1461638,Human_Splice_Rec_1461656,Human_Splice_Rec_1461670,Human_Splice_Rec_1461682,Human_Splice_Rec_1461700,Human_Splice_Rec_1461704 RMVar_hsa_circ_78306,RMVar_hsa_circ_126449,RMVar_hsa_circ_163183,RMVar_hsa_circ_163184 47349 RMVar_ID_47349 Human_SNP_ID_529139433 A-to-I Human chr13 + 45344383 45344383 45344383 TCGGCTCACTGCAACCTCTGGCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCCCCTGAGTAGC TCGGCTCACTGCAACCTCTGGCTCCCAGGTTCGAGCGATTCTCCTGCCTCAGCCCCCTGAGTAGC A G TPT1-AS1 Ensembl:ENSG00000170919 lincRNA exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs727799 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1461293,Human_Splice_Rec_1461416,Human_Splice_Rec_1461417,Human_Splice_Rec_1461444,Human_Splice_Rec_1461445,Human_Splice_Rec_1461452,Human_Splice_Rec_1461453,Human_Splice_Rec_1461488,Human_Splice_Rec_1461489,Human_Splice_Rec_1461598,Human_Splice_Rec_1461599,Human_Splice_Rec_1461616,Human_Splice_Rec_1461617,Human_Splice_Rec_1461620,Human_Splice_Rec_1461621,Human_Splice_Rec_1461638,Human_Splice_Rec_1461639,Human_Splice_Rec_1461656,Human_Splice_Rec_1461657,Human_Splice_Rec_1461670,Human_Splice_Rec_1461671,Human_Splice_Rec_1461682,Human_Splice_Rec_1461683,Human_Splice_Rec_1461700,Human_Splice_Rec_1461701,Human_Splice_Rec_1461704,Human_Splice_Rec_1461705,Human_Splice_Rec_1461707,Human_Splice_Rec_1461715,Human_Splice_Rec_1461727,Human_Splice_Rec_1461745,Human_Splice_Rec_1461763,Human_Splice_Rec_1461781,Human_Splice_Rec_1461797,Human_Splice_Rec_1461815 RMVar_hsa_circ_78306,RMVar_hsa_circ_126449,RMVar_hsa_circ_163183,RMVar_hsa_circ_122316,RMVar_hsa_circ_163184,RMVar_hsa_circ_163185 47350 RMVar_ID_47350 Human_SNP_ID_529139441 A-to-I Human chr13 + 45344401 45344401 45344401 TGGCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCCCCTGAGTAGCTGGGATTACAGGCACGCG TGGCTCCCAGGTTCAAGCGATTCTCCTGCCTCGGCCCCCTGAGTAGCTGGGATTACAGGCACGCG A G TPT1-AS1 Ensembl:ENSG00000170919 lincRNA exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1342376222 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1461293,Human_Splice_Rec_1461416,Human_Splice_Rec_1461417,Human_Splice_Rec_1461444,Human_Splice_Rec_1461445,Human_Splice_Rec_1461452,Human_Splice_Rec_1461453,Human_Splice_Rec_1461488,Human_Splice_Rec_1461489,Human_Splice_Rec_1461598,Human_Splice_Rec_1461599,Human_Splice_Rec_1461616,Human_Splice_Rec_1461617,Human_Splice_Rec_1461620,Human_Splice_Rec_1461621,Human_Splice_Rec_1461638,Human_Splice_Rec_1461639,Human_Splice_Rec_1461656,Human_Splice_Rec_1461657,Human_Splice_Rec_1461670,Human_Splice_Rec_1461671,Human_Splice_Rec_1461682,Human_Splice_Rec_1461683,Human_Splice_Rec_1461700,Human_Splice_Rec_1461701,Human_Splice_Rec_1461704,Human_Splice_Rec_1461705,Human_Splice_Rec_1461707,Human_Splice_Rec_1461715,Human_Splice_Rec_1461727,Human_Splice_Rec_1461745,Human_Splice_Rec_1461763,Human_Splice_Rec_1461781,Human_Splice_Rec_1461797,Human_Splice_Rec_1461815 RMVar_hsa_circ_78306,RMVar_hsa_circ_126449,RMVar_hsa_circ_163183,RMVar_hsa_circ_122316,RMVar_hsa_circ_163184,RMVar_hsa_circ_163185 47351 RMVar_ID_47351 Human_SNP_ID_529139964 A-to-I Human chr13 + 45346076 45346076 45346076 CTCATTCTGTTGCCCAGGCTGTGAAGCGGCACAATCACAGCTCACTGCAGCCTCCACCTCCCTCC CTCATTCTGTTGCCCAGGCTGTGAAGCGGCACGATCACAGCTCACTGCAGCCTCCACCTCCCTCC A G TPT1-AS1 Ensembl:ENSG00000170919 lincRNA intron GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-Seq:(High) rs535213545 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8249183,Human_RBP_ID_22711120 RMVar_hsa_circ_126449,RMVar_hsa_circ_163183,RMVar_hsa_circ_122316,RMVar_hsa_circ_163185 47352 RMVar_ID_47352 Human_SNP_ID_529140225 A-to-I Human chr13 + 45346924 45346924 45346924 ACCTCAGGTGATCTGCCCACCTCGGCCTCCCAAAGTGCTGACATTACAGGTGTGAGCCACCATGC ACCTCAGGTGATCTGCCCACCTCGGCCTCCCAGAGTGCTGACATTACAGGTGTGAGCCACCATGC A G TPT1-AS1 Ensembl:ENSG00000170919 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs747895167 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126449,RMVar_hsa_circ_163183,RMVar_hsa_circ_122316,RMVar_hsa_circ_163185 47353 RMVar_ID_47353 Human_SNP_ID_529140271 A-to-I Human chr13 + 45347114 45347103 45347115 GCCTATGGCTGGGTGCAGTGGCTCATACCTGTAATCACAGCACTTTGGGAGGCCAGGGTGGGCAA GCCTATGGCTGGGTGCAGTGGC____________TCACAGCACTTTGGGAGGCCAGGGTGGGCAA CTCATACCTGTAA C TPT1-AS1 Ensembl:ENSG00000170919 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1311103313 Functional Loss DEL dbSNP153 23..34 33 - - - RMVar_hsa_circ_126449,RMVar_hsa_circ_163183,RMVar_hsa_circ_122316,RMVar_hsa_circ_163185 47354 RMVar_ID_47354 Human_SNP_ID_529140305 A-to-I Human chr13 + 45347236 45347236 45347236 AAACCCTATCTCTACTAAAAATACAAAAAATTAGCTGAGCCTGGTGGCATGGGTCTGTAATCCCA AAACCCTATCTCTACTAAAAATACAAAAAATTGGCTGAGCCTGGTGGCATGGGTCTGTAATCCCA A G TPT1-AS1 Ensembl:ENSG00000170919 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs753030663 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126449,RMVar_hsa_circ_163183,RMVar_hsa_circ_122316,RMVar_hsa_circ_163185 47355 RMVar_ID_47355 Human_SNP_ID_529141617 A-to-I Human chr13 + 45351239 45351239 45351239 GAACTCCTGAGCTGAGGCAATCCTCCCGCCTCAGCCTCCGCAGTAGTTGGGATTACAGGTGTGAG GAACTCCTGAGCTGAGGCAATCCTCCCGCCTCGGCCTCCGCAGTAGTTGGGATTACAGGTGTGAG A G AL138963.1,TPT1-AS1 Ensembl:ENSG00000228886,Ensembl:ENSG00000170919 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs912289371 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5175354 RMVar_hsa_circ_126449,RMVar_hsa_circ_163183,RMVar_hsa_circ_122316,RMVar_hsa_circ_163185 47356 RMVar_ID_47356 Human_SNP_ID_529141786 A-to-I Human chr13 + 45351895 45351895 45351895 CCCGGTTTTTGTTCTGTTTTCGTTTTTGGGACAGGGTCTTACTCTGTGACCCACGCTGGAGTGCA CCCGGTTTTTGTTCTGTTTTCGTTTTTGGGACCGGGTCTTACTCTGTGACCCACGCTGGAGTGCA A C TPT1-AS1 Ensembl:ENSG00000170919 lincRNA intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1566182140 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_756194,Human_RBP_ID_811986,Human_RBP_ID_5246705,Human_RBP_ID_12253740 RMVar_hsa_circ_126449,RMVar_hsa_circ_163183,RMVar_hsa_circ_122316,RMVar_hsa_circ_163185 47357 RMVar_ID_47357 Human_SNP_ID_529141808 A-to-I Human chr13 + 45351971 45351971 45351971 ACGACTTACTGAAGCCTCCACTTCCCGGGCTCAAGTGATTCTCACACCTCAGCCTCCTGAGTAGC ACGACTTACTGAAGCCTCCACTTCCCGGGCTCCAGTGATTCTCACACCTCAGCCTCCTGAGTAGC A C TPT1-AS1 Ensembl:ENSG00000170919 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1443522673 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1461420,Human_Splice_Rec_1461421,Human_Splice_Rec_1461424,Human_Splice_Rec_1461425,Human_Splice_Rec_1461718,Human_Splice_Rec_1461719,Human_Splice_Rec_1461831 RMVar_hsa_circ_126449,RMVar_hsa_circ_163183,RMVar_hsa_circ_122316,RMVar_hsa_circ_163185 47358 RMVar_ID_47358 Human_SNP_ID_529142318 A-to-I Human chr13 + 45353409 45353404 45353409 TTTTTTTTTTTAAATAGAGACATGGTCTTAGTATATTGTCTGGGCTGGTCTCAAACTCCTGGGCT TTTTTTTTTTTAAATAGAGACATGGTCT_____TATTGTCTGGGCTGGTCTCAAACTCCTGGGCT TTAGTA T TPT1-AS1 Ensembl:ENSG00000170919 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1385771045 Functional Loss DEL dbSNP153 29..33 33 - - - Human_RBP_ID_118430,Human_RBP_ID_12166720 RMVar_hsa_circ_126449,RMVar_hsa_circ_163183,RMVar_hsa_circ_122316,RMVar_hsa_circ_163185 47359 RMVar_ID_47359 Human_SNP_ID_529142319 A-to-I Human chr13 + 45353409 45353409 45353409 TTTTTTTTTTTAAATAGAGACATGGTCTTAGTATATTGTCTGGGCTGGTCTCAAACTCCTGGGCT TTTTTTTTTTTAAATAGAGACATGGTCTTAGTGTATTGTCTGGGCTGGTCTCAAACTCCTGGGCT A G TPT1-AS1 Ensembl:ENSG00000170919 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474694907 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_118430,Human_RBP_ID_12166720 RMVar_hsa_circ_126449,RMVar_hsa_circ_163183,RMVar_hsa_circ_122316,RMVar_hsa_circ_163185 47360 RMVar_ID_47360 Human_SNP_ID_529142355 A-to-I Human chr13 + 45353575 45353575 45353575 CACTTTGGGAGGCTGAGGAGGGAGGATCACTTAAGGCCAGGAGTTTGAGAACAAGACCAGCCTGG CACTTTGGGAGGCTGAGGAGGGAGGATCACTTGAGGCCAGGAGTTTGAGAACAAGACCAGCCTGG A G TPT1-AS1 Ensembl:ENSG00000170919 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs560437057 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126449,RMVar_hsa_circ_163183,RMVar_hsa_circ_122316,RMVar_hsa_circ_163185 47361 RMVar_ID_47361 Human_SNP_ID_529142408 A-to-I Human chr13 + 45353755 45353755 45353755 CTGGGAGGTTGAGGTTGCAGTGAGCCGTGTTCATGCTACTGTACTCCAGCCTGGGTGATAGAGTG CTGGGAGGTTGAGGTTGCAGTGAGCCGTGTTCGTGCTACTGTACTCCAGCCTGGGTGATAGAGTG A G TPT1-AS1 Ensembl:ENSG00000170919 lincRNA intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs538096485 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25078807 RMVar_hsa_circ_126449,RMVar_hsa_circ_163183,RMVar_hsa_circ_122316,RMVar_hsa_circ_163185 47362 RMVar_ID_47362 Human_SNP_ID_529142668 A-to-I Human chr13 + 45354626 45354626 45354626 TCGGCTCACTGCCACCTTTGCCTCCTGGGTTCAAGTGATTCTCCTGCCTCAGCCTTCCAGATAGC TCGGCTCACTGCCACCTTTGCCTCCTGGGTTCCAGTGATTCTCCTGCCTCAGCCTTCCAGATAGC A C TPT1-AS1 Ensembl:ENSG00000170919 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1272897887 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126449,RMVar_hsa_circ_163183,RMVar_hsa_circ_122316,RMVar_hsa_circ_163185 47363 RMVar_ID_47363 Human_SNP_ID_529142790 A-to-I Human chr13 + 45355112 45355098 45355112 CTAGTACCTCAGCCTCCCGAGTAGCCAGGATTACAGGCACATGCCAGCACGCCTGGGTAATTTTT CTAGTACCTCAGCCTCCCG______________CAGGCACATGCCAGCACGCCTGGGTAATTTTT GAGTAGCCAGGATTA G TPT1-AS1 Ensembl:ENSG00000170919 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1249782623 Functional Loss DEL dbSNP153 20..33 33 - - - RMVar_hsa_circ_126449,RMVar_hsa_circ_163183,RMVar_hsa_circ_122316,RMVar_hsa_circ_163185 47364 RMVar_ID_47364 Human_SNP_ID_529142793 A-to-I Human chr13 + 45355112 45355112 45355112 CTAGTACCTCAGCCTCCCGAGTAGCCAGGATTACAGGCACATGCCAGCACGCCTGGGTAATTTTT CTAGTACCTCAGCCTCCCGAGTAGCCAGGATTGCAGGCACATGCCAGCACGCCTGGGTAATTTTT A G TPT1-AS1 Ensembl:ENSG00000170919 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1423119414 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126449,RMVar_hsa_circ_163183,RMVar_hsa_circ_122316,RMVar_hsa_circ_163185 47365 RMVar_ID_47365 Human_SNP_ID_529143598 A-to-I Human chr13 + 45358218 45358218 45358218 TCGGCTCACTGCAACCTCTGCCTCCCAGGTTCAAGCAGTTCTCCTGCCCCAGCCTCCTGAGTAGC TCGGCTCACTGCAACCTCTGCCTCCCAGGTTCGAGCAGTTCTCCTGCCCCAGCCTCCTGAGTAGC A G TPT1-AS1 Ensembl:ENSG00000170919 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1331672517 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126449,RMVar_hsa_circ_163183,RMVar_hsa_circ_122316,RMVar_hsa_circ_163185 47366 RMVar_ID_47366 Human_SNP_ID_529143619 A-to-I Human chr13 + 45358298 45358298 45358298 ACTTTTCGCTGGGTGCGGCGGCTCACGCCTGTAATCTCAGCACTTTGGGTGGCTGAGGTGGATGG ACTTTTCGCTGGGTGCGGCGGCTCACGCCTGTCATCTCAGCACTTTGGGTGGCTGAGGTGGATGG A C TPT1-AS1 Ensembl:ENSG00000170919 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1236741507 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17562004,Human_RBP_ID_25052613 RMVar_hsa_circ_126449,RMVar_hsa_circ_163183,RMVar_hsa_circ_122316,RMVar_hsa_circ_163185 47367 RMVar_ID_47367 Human_SNP_ID_529143992 A-to-I Human chr13 + 45359240 45359240 45359240 GCTGGAGTACAGTGGCACGATCTCGGCTCACTACAAGCTCCGCCTCCTGGGTTCACGCCACTTTC GCTGGAGTACAGTGGCACGATCTCGGCTCACTGCAAGCTCCGCCTCCTGGGTTCACGCCACTTTC A G TPT1-AS1 Ensembl:ENSG00000170919 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900272851 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126449,RMVar_hsa_circ_163183,RMVar_hsa_circ_122316,RMVar_hsa_circ_163185 47368 RMVar_ID_47368 Human_SNP_ID_529144280 A-to-I Human chr13 + 45360198 45360198 45360198 GCTGGAGTGCAATGGCAAGATCTCAGCTCACCACAACCTCTGCCTTCTTTTTTCTTCTGTTTTTA GCTGGAGTGCAATGGCAAGATCTCAGCTCACCGCAACCTCTGCCTTCTTTTTTCTTCTGTTTTTA A G TPT1-AS1 Ensembl:ENSG00000170919 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs967770939 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1461446,Human_Splice_Rec_1461447,Human_Splice_Rec_1461706 RMVar_hsa_circ_126449,RMVar_hsa_circ_163183,RMVar_hsa_circ_122316,RMVar_hsa_circ_163185 47369 RMVar_ID_47369 Human_SNP_ID_529144489 A-to-I Human chr13 + 45360849 45360849 45360849 GCCACTGCGCTGGAATGCAATGACACGATCTCAGCTCACTGCAACCTCTGCCTCTCGGGTTCAAG GCCACTGCGCTGGAATGCAATGACACGATCTCGGCTCACTGCAACCTCTGCCTCTCGGGTTCAAG A G TPT1-AS1 Ensembl:ENSG00000170919 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1392380863 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126449,RMVar_hsa_circ_163183,RMVar_hsa_circ_122316,RMVar_hsa_circ_163185 47370 RMVar_ID_47370 Human_SNP_ID_529146961 A-to-I Human chr13 + 45369716 45369716 45369716 ATGGCTCACTCTAGCCTCTGCCTCCCAGTCTCAAGCAATCCTCCCACCTCAGCCTCCCAAGTAGG ATGGCTCACTCTAGCCTCTGCCTCCCAGTCTCTAGCAATCCTCCCACCTCAGCCTCCCAAGTAGG A T TPT1-AS1 Ensembl:ENSG00000170919 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1181396093 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126449,RMVar_hsa_circ_163183,RMVar_hsa_circ_122316,RMVar_hsa_circ_163185 47371 RMVar_ID_47371 Human_SNP_ID_529148159 A-to-I Human chr13 + 45374178 45374178 45374178 GTTGGCCAGGCTGGTCTCGAACTCATGACCTCAGGAGGTCTGCCTGCCTCGGCCTCCCAAAGTGC GTTGGCCAGGCTGGTCTCGAACTCATGACCTCGGGAGGTCTGCCTGCCTCGGCCTCCCAAAGTGC A G TPT1-AS1 Ensembl:ENSG00000170919 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1458126975 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126449,RMVar_hsa_circ_163183,RMVar_hsa_circ_122316,RMVar_hsa_circ_163185 47372 RMVar_ID_47372 Human_SNP_ID_529148523 A-to-I Human chr13 + 45375819 45375818 45375819 CAGGAATTCTAGACCAGCCTGGCCAACATGACAAAACCCCTTCTCTACTAAAAATACAAAAAATT CAGGAATTCTAGACCAGCCTGGCCAACATGAC_AAACCCCTTCTCTACTAAAAATACAAAAAATT CA C TPT1-AS1 Ensembl:ENSG00000170919 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1566188661 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_8249884 RMVar_hsa_circ_126449,RMVar_hsa_circ_163183,RMVar_hsa_circ_122316,RMVar_hsa_circ_163185 47373 RMVar_ID_47373 Human_SNP_ID_529148525 A-to-I Human chr13 + 45375819 45375819 45375819 CAGGAATTCTAGACCAGCCTGGCCAACATGACAAAACCCCTTCTCTACTAAAAATACAAAAAATT CAGGAATTCTAGACCAGCCTGGCCAACATGACGAAACCCCTTCTCTACTAAAAATACAAAAAATT A G TPT1-AS1 Ensembl:ENSG00000170919 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1383461887 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8249884 RMVar_hsa_circ_126449,RMVar_hsa_circ_163183,RMVar_hsa_circ_122316,RMVar_hsa_circ_163185 47374 RMVar_ID_47374 Human_SNP_ID_529148533 A-to-I Human chr13 + 45375860 45375860 45375860 TCTCTACTAAAAATACAAAAAATTAGCCAGGCATGGTGGCAGATGCCTGTAATCCCAGCTATTTG TCTCTACTAAAAATACAAAAAATTAGCCAGGCGTGGTGGCAGATGCCTGTAATCCCAGCTATTTG A G TPT1-AS1 Ensembl:ENSG00000170919 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1444650568 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126449,RMVar_hsa_circ_163183,RMVar_hsa_circ_122316,RMVar_hsa_circ_163185 47375 RMVar_ID_47375 Human_SNP_ID_529148535 A-to-I Human chr13 + 45375868 45375868 45375868 AAAAATACAAAAAATTAGCCAGGCATGGTGGCAGATGCCTGTAATCCCAGCTATTTGGGAGGCTG AAAAATACAAAAAATTAGCCAGGCATGGTGGCGGATGCCTGTAATCCCAGCTATTTGGGAGGCTG A G TPT1-AS1 Ensembl:ENSG00000170919 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs945977981 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126449,RMVar_hsa_circ_163183,RMVar_hsa_circ_122316,RMVar_hsa_circ_163185 47376 RMVar_ID_47376 Human_SNP_ID_529148623 A-to-I Human chr13 + 45376216 45376216 45376216 CACGAGGTCAGGAGATCGAGACCATCCTGGCTAACATGGTGAAACCCCATCTCTACTAAAAACAC CACGAGGTCAGGAGATCGAGACCATCCTGGCTTACATGGTGAAACCCCATCTCTACTAAAAACAC A T TPT1-AS1 Ensembl:ENSG00000170919 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs887552281 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126449,RMVar_hsa_circ_163183,RMVar_hsa_circ_122316,RMVar_hsa_circ_163185 47377 RMVar_ID_47377 Human_SNP_ID_529148657 A-to-I Human chr13 + 45376316 45376316 45376316 TCTGTAGTCCCAGCTACTAGGGAAGCTGAGGCAGGAGAATGGTGTAAGCTTGCAGTGAGCAGAGA TCTGTAGTCCCAGCTACTAGGGAAGCTGAGGCCGGAGAATGGTGTAAGCTTGCAGTGAGCAGAGA A C TPT1-AS1 Ensembl:ENSG00000170919 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs967216903 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126449,RMVar_hsa_circ_163183,RMVar_hsa_circ_122316,RMVar_hsa_circ_163185 47378 RMVar_ID_47378 Human_SNP_ID_529153372 A-to-I Human chr13 + 45385224 45385224 45385224 CAGGCGTGGTGGCTCACGCCTGCAATCCCAACACTTTGGGAGGCCAAGGCGGGAGGATCACTTGA CAGGCGTGGTGGCTCACGCCTGCAATCCCAACGCTTTGGGAGGCCAAGGCGGGAGGATCACTTGA A G TPT1-AS1 Ensembl:ENSG00000170919 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs928942556 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126449,RMVar_hsa_circ_163183,RMVar_hsa_circ_163186 47379 RMVar_ID_47379 Human_SNP_ID_529153606 A-to-I Human chr13 + 45386261 45386261 45386261 TGGGGTCTCCCTACATTGCCCAGGCTGGTCTCAAACTCTTAGGCTCAAGTGATACTCTCGCCTTG TGGGGTCTCCCTACATTGCCCAGGCTGGTCTCGAACTCTTAGGCTCAAGTGATACTCTCGCCTTG A G TPT1-AS1 Ensembl:ENSG00000170919 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1410336786 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126449,RMVar_hsa_circ_163183,RMVar_hsa_circ_163186 47380 RMVar_ID_47380 Human_SNP_ID_529153608 A-to-I Human chr13 + 45386269 45386269 45386269 CCCTACATTGCCCAGGCTGGTCTCAAACTCTTAGGCTCAAGTGATACTCTCGCCTTGGCCTCCCA CCCTACATTGCCCAGGCTGGTCTCAAACTCTTTGGCTCAAGTGATACTCTCGCCTTGGCCTCCCA A T TPT1-AS1 Ensembl:ENSG00000170919 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs942718736 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126449,RMVar_hsa_circ_163183,RMVar_hsa_circ_163186 47381 RMVar_ID_47381 Human_SNP_ID_529157189 A-to-I Human chr13 - 45400743 45400736 45400743 CCTGTAATCTTAGGACTTTGGAAGGCCGAGGCAGGAGGATCACTTGAGCCTAGGAATTCAAGACC CCTGTAATCTTAGGACTTTGGAAGGCCGAGGC_______TCACTTGAGCCTAGGAATTCAAGACC ATCCTCCT A SLC25A30 Ensembl:ENSG00000174032 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1160880116 Functional Loss DEL dbSNP153 33..39 33 - - - RMVar_hsa_circ_60502,RMVar_hsa_circ_338087,RMVar_hsa_circ_267666,RMVar_hsa_circ_267870,RMVar_hsa_circ_348619,RMVar_hsa_circ_8126,RMVar_hsa_circ_51952 47382 RMVar_ID_47382 Human_SNP_ID_529160851 A-to-I Human chr13 - 45417106 45417106 45417106 GGGAGGTTGAGACAGGAGAATCGCTTGAATCCAGGAGACGGAGGTTGCAGTGAGCCGAGATCATG GGGAGGTTGAGACAGGAGAATCGCTTGAATCCGGGAGACGGAGGTTGCAGTGAGCCGAGATCATG T C SLC25A30 Ensembl:ENSG00000174032 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1359259457 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95598,RMVar_hsa_circ_163196 47383 RMVar_ID_47383 Human_SNP_ID_529178868 A-to-I Human chr13 + 45475845 45475845 45475845 AAAATTAGCTGGGCGTGGTGTTGCGTGCCTGTAATCTCAGCTACTTGGAGATTGAGGTGGGAGGA AAAATTAGCTGGGCGTGGTGTTGCGTGCCTGTCATCTCAGCTACTTGGAGATTGAGGTGGGAGGA A C COG3 Ensembl:ENSG00000136152 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1371443985 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_163201,RMVar_hsa_circ_102914 47384 RMVar_ID_47384 Human_SNP_ID_529184439 A-to-I Human chr13 + 45497741 45497741 45497741 CCGGGAGGTGGAGGTTTCAGGGAGCCGAGATCACGCCATTGCACTCCAGCCTGGGTGACAGAGCC CCGGGAGGTGGAGGTTTCAGGGAGCCGAGATCGCGCCATTGCACTCCAGCCTGGGTGACAGAGCC A G COG3 Ensembl:ENSG00000136152 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1566255702 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_163201,RMVar_hsa_circ_102914,RMVar_hsa_circ_355674,RMVar_hsa_circ_19911,RMVar_hsa_circ_64321,RMVar_hsa_circ_88620,RMVar_hsa_circ_84243,RMVar_hsa_circ_163205,RMVar_hsa_circ_163206,RMVar_hsa_circ_361642,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_54143,RMVar_hsa_circ_268577,RMVar_hsa_circ_357547,RMVar_hsa_circ_372022,RMVar_hsa_circ_64536,RMVar_hsa_circ_34821,RMVar_hsa_circ_54049,RMVar_hsa_circ_344529,RMVar_hsa_circ_163211,RMVar_hsa_circ_59967,RMVar_hsa_circ_35785 47385 RMVar_ID_47385 Human_SNP_ID_529189566 A-to-I Human chr13 + 45518300 45518300 45518300 TGAGACCTCAGCTAATACTTCACATAGATTCTAGTTAGTCTGGAGGTTAAGGGGTAAATACGTCC TGAGACCTCAGCTAATACTTCACATAGATTCTCGTTAGTCTGGAGGTTAAGGGGTAAATACGTCC A C COG3 Ensembl:ENSG00000136152 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs772748344 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6286422,Human_RBP_ID_9733502,Human_RBP_ID_17838618,Human_RBP_ID_21920992 RMVar_hsa_circ_34300,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_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_35785,RMVar_hsa_circ_343034,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 47386 RMVar_ID_47386 Human_SNP_ID_529190009 A-to-I Human chr13 + 45520168 45520168 45520168 AAAATTAGCCATGTGTAGTGGCGTGTGCCTATAGTCCCAGGTACTTGGGAGGCTGAGGTGGGAAG AAAATTAGCCATGTGTAGTGGCGTGTGCCTATGGTCCCAGGTACTTGGGAGGCTGAGGTGGGAAG A G COG3 Ensembl:ENSG00000136152 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1229676692 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34300,RMVar_hsa_circ_64321,RMVar_hsa_circ_57372,RMVar_hsa_circ_93417,RMVar_hsa_circ_163210,RMVar_hsa_circ_31649,RMVar_hsa_circ_268577,RMVar_hsa_circ_372022,RMVar_hsa_circ_64536,RMVar_hsa_circ_163211,RMVar_hsa_circ_35785,RMVar_hsa_circ_163220,RMVar_hsa_circ_282217,RMVar_hsa_circ_283326,RMVar_hsa_circ_276408,RMVar_hsa_circ_163218,RMVar_hsa_circ_163219,RMVar_hsa_circ_163217,RMVar_hsa_circ_163221,RMVar_hsa_circ_55743,RMVar_hsa_circ_371892 47387 RMVar_ID_47387 Human_SNP_ID_529311589 A-to-I Human chr13 - 46025443 46025443 46025443 TTAATTAGCTGGGCGTAGTGGTATGTACCAGTAGTTCCAGCTGTGGGAGGCTGAGGCAGGAGGAT TTAATTAGCTGGGCGTAGTGGTATGTACCAGTCGTTCCAGCTGTGGGAGGCTGAGGCAGGAGGAT T G ZC3H13 Ensembl:ENSG00000123200 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1359679968 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6286917,Human_RBP_ID_12168589,Human_RBP_ID_25053133 RMVar_hsa_circ_57629,RMVar_hsa_circ_368433,RMVar_hsa_circ_163224,RMVar_hsa_circ_115941,RMVar_hsa_circ_364174,RMVar_hsa_circ_327924,RMVar_hsa_circ_163226,RMVar_hsa_circ_80669,RMVar_hsa_circ_351858,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_348215,RMVar_hsa_circ_163234,RMVar_hsa_circ_163239,RMVar_hsa_circ_356868,RMVar_hsa_circ_350526,RMVar_hsa_circ_163237,RMVar_hsa_circ_285208,RMVar_hsa_circ_346984,RMVar_hsa_circ_288200,RMVar_hsa_circ_346327,RMVar_hsa_circ_163238,RMVar_hsa_circ_356040,RMVar_hsa_circ_163242,RMVar_hsa_circ_36649,RMVar_hsa_circ_163243,RMVar_hsa_circ_271564,RMVar_hsa_circ_359845,RMVar_hsa_circ_299504,RMVar_hsa_circ_163244 47388 RMVar_ID_47388 Human_SNP_ID_529314223 A-to-I Human chr13 - 46036898 46036898 46036898 ACTGGCCAACATAGCAAAACCCCGTCTCTACTAAAAATGCAAAAATTAGCCAGGTGTGGTGGCTC ACTGGCCAACATAGCAAAACCCCGTCTCTACTGAAAATGCAAAAATTAGCCAGGTGTGGTGGCTC T C ZC3H13 Ensembl:ENSG00000123200 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1273943262 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57629,RMVar_hsa_circ_368433,RMVar_hsa_circ_163224,RMVar_hsa_circ_115941,RMVar_hsa_circ_364174,RMVar_hsa_circ_327924,RMVar_hsa_circ_163226,RMVar_hsa_circ_80669,RMVar_hsa_circ_351858,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_348215,RMVar_hsa_circ_163234,RMVar_hsa_circ_163239,RMVar_hsa_circ_356868,RMVar_hsa_circ_350526,RMVar_hsa_circ_163237,RMVar_hsa_circ_285208,RMVar_hsa_circ_346984,RMVar_hsa_circ_288200,RMVar_hsa_circ_346327,RMVar_hsa_circ_163238,RMVar_hsa_circ_356040,RMVar_hsa_circ_163242,RMVar_hsa_circ_36649,RMVar_hsa_circ_163243,RMVar_hsa_circ_271564,RMVar_hsa_circ_359845,RMVar_hsa_circ_299504,RMVar_hsa_circ_163244 47389 RMVar_ID_47389 Human_SNP_ID_529337736 A-to-I Human chr13 - 46138723 46138723 46138723 AGAATCTCTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCCAAGATCATGCCACTGCACTCCAGCC AGAATCTCTTGAACCTGGGAGGCAGAGGTTGCGGTGAGCCAAGATCATGCCACTGCACTCCAGCC T C LCP1 Ensembl:ENSG00000136167 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs780116233 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33212,RMVar_hsa_circ_61002,RMVar_hsa_circ_57429,RMVar_hsa_circ_52949,RMVar_hsa_circ_60033 47390 RMVar_ID_47390 Human_SNP_ID_529476076 A-to-I Human chr13 + 46724257 46724257 46724257 ATTTTTAAGAGACTCTCTCTGTTGCCCAGACTAGAGTGCAATGGTATGATCATAGCTGACTGCAG ATTTTTAAGAGACTCTCTCTGTTGCCCAGACTTGAGTGCAATGGTATGATCATAGCTGACTGCAG A T LRCH1 Ensembl:ENSG00000136141 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1302537536 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74667,RMVar_hsa_circ_122895,RMVar_hsa_circ_163259,RMVar_hsa_circ_163270,RMVar_hsa_circ_616,RMVar_hsa_circ_163260,RMVar_hsa_circ_98121,RMVar_hsa_circ_82099,RMVar_hsa_circ_319930,RMVar_hsa_circ_163266,RMVar_hsa_circ_28199,RMVar_hsa_circ_163271,RMVar_hsa_circ_163272,RMVar_hsa_circ_313776,RMVar_hsa_circ_100874,RMVar_hsa_circ_163273,RMVar_hsa_circ_61827,RMVar_hsa_circ_163282,RMVar_hsa_circ_98738,RMVar_hsa_circ_339757,RMVar_hsa_circ_163278,RMVar_hsa_circ_163279,RMVar_hsa_circ_348362,RMVar_hsa_circ_56192,RMVar_hsa_circ_163281,RMVar_hsa_circ_163280,RMVar_hsa_circ_108361,RMVar_hsa_circ_271604,RMVar_hsa_circ_100373,RMVar_hsa_circ_276258,RMVar_hsa_circ_284682,RMVar_hsa_circ_163283,RMVar_hsa_circ_163284 47391 RMVar_ID_47391 Human_SNP_ID_529722942 A-to-I Human chr13 + 47763633 47763633 47763633 CTTGCAGCCCTTCAAGAAAGACTTGATGGTCTAATAGAAACACCAACAGGATACATTGAAAGCCT CTTGCAGCCCTTCAAGAAAGACTTGATGGTCTGATAGAAACACCAACAGGATACATTGAAAGCCT A G NAP1L4P3 Ensembl:ENSG00000234145 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1032451635 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6314927 47392 RMVar_ID_47392 Human_SNP_ID_529722962 A-to-I Human chr13 + 47763686 47763686 47763686 CATTGAAAGCCTGCCTAGGGTAGTTAAAAAACAAGTGAATGCTCTCAAACACCTGTAAGTTAAAT CATTGAAAGCCTGCCTAGGGTAGTTAAAAAACGAGTGAATGCTCTCAAACACCTGTAAGTTAAAT A G NAP1L4P3 Ensembl:ENSG00000234145 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1379231542 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1818678 47393 RMVar_ID_47393 Human_SNP_ID_529764202 A-to-I Human chr13 - 47941930 47941930 47941930 TTGCCCAGGCTGGAGTGCTGTTGCACGATCTCAGCTCACTGCAAGCTCCGCCTCTGGGGTTCACA TTGCCCAGGCTGGAGTGCTGTTGCACGATCTCGGCTCACTGCAAGCTCCGCCTCTGGGGTTCACA T C SUCLA2 Ensembl:ENSG00000136143 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1382523918 Functional Loss SNV dbSNP153 33..33 33 - - - 47394 RMVar_ID_47394 Human_SNP_ID_529764265 A-to-I Human chr13 - 47942235 47942235 47942235 GCTTTGCCTCCCAAAATGTTGAGATTACATGTATGAACTACTGCACCCAGCCAACCATACATATT GCTTTGCCTCCCAAAATGTTGAGATTACATGTGTGAACTACTGCACCCAGCCAACCATACATATT T C SUCLA2 Ensembl:ENSG00000136143 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006251052 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8392870,Human_RBP_ID_12171527 47395 RMVar_ID_47395 Human_SNP_ID_529769612 A-to-I Human chr13 - 47963582 47963582 47963582 GGAGTGCAGTGGCGTGATCTCAGCTCACTGCAACCTCCGCCTCCCGGGTTCAGGCGATTCTCCTG GGAGTGCAGTGGCGTGATCTCAGCTCACTGCAGCCTCCGCCTCCCGGGTTCAGGCGATTCTCCTG T C SUCLA2 Ensembl:ENSG00000136143 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs932552332 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18817,RMVar_hsa_circ_273015,RMVar_hsa_circ_326513,RMVar_hsa_circ_163293,RMVar_hsa_circ_73993 47396 RMVar_ID_47396 Human_SNP_ID_529771871 A-to-I Human chr13 - 47972133 47972133 47972133 CTCCTGCCTCAGCCTACCGACTAGCTGGGACTACAGGCGCACGTCACCATGCCCGGCTAATTTTT CTCCTGCCTCAGCCTACCGACTAGCTGGGACTGCAGGCGCACGTCACCATGCCCGGCTAATTTTT T C SUCLA2 Ensembl:ENSG00000136143 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs370343750 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18817,RMVar_hsa_circ_326513,RMVar_hsa_circ_43623,RMVar_hsa_circ_339121,RMVar_hsa_circ_73993,RMVar_hsa_circ_280686,RMVar_hsa_circ_163294,RMVar_hsa_circ_163295 47397 RMVar_ID_47397 Human_SNP_ID_529792187 A-to-I Human chr13 - 48050297 48050297 48050297 TCACTGTAGCCTCGATATCCTGGGCTCAAGCAATCCTCCCACCTCAGCCTCCCAAGGAGCTGGGA TCACTGTAGCCTCGATATCCTGGGCTCAAGCAGTCCTCCCACCTCAGCCTCCCAAGGAGCTGGGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs551414326 Functional Loss SNV dbSNP153 33..33 33 - - - 47398 RMVar_ID_47398 Human_SNP_ID_529792188 A-to-I Human chr13 - 48050297 48050297 48050297 TCACTGTAGCCTCGATATCCTGGGCTCAAGCAATCCTCCCACCTCAGCCTCCCAAGGAGCTGGGA TCACTGTAGCCTCGATATCCTGGGCTCAAGCACTCCTCCCACCTCAGCCTCCCAAGGAGCTGGGA T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs551414326 Functional Loss SNV dbSNP153 33..33 33 - - - 47399 RMVar_ID_47399 Human_SNP_ID_529795508 A-to-I Human chr13 - 48063208 48063208 48063208 TGTAATTATTTTATTTTTTGAGACAGTGTCTCACTCCATCACCCGGGCTGGAGTGCAGTGGCATG TGTAATTATTTTATTTTTTGAGACAGTGTCTCGCTCCATCACCCGGGCTGGAGTGCAGTGGCATG T C MED4 Ensembl:ENSG00000136146 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1225788592 Functional Loss SNV dbSNP153 33..33 33 - - - 47400 RMVar_ID_47400 Human_SNP_ID_529795699 A-to-I Human chr13 - 48064107 48064107 48064107 AGTTGGGTGTGGTGGCGTGCACCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATTGCT AGTTGGGTGTGGTGGCGTGCACCTGTAGTCCCGGCTACTTGGGAGGCTGAGGCAGGAGAATTGCT T C MED4 Ensembl:ENSG00000136146 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270539872 Functional Loss SNV dbSNP153 33..33 33 - - - 47401 RMVar_ID_47401 Human_SNP_ID_529872711 A-to-I Human chr13 + 48391477 48391477 48391477 TTTTCCTTCTGACTGTAAAACTTTTTTTGGCCAGGGGCAGTGGCTCATACCCGTAATCCCAACAC TTTTCCTTCTGACTGTAAAACTTTTTTTGGCCGGGGGCAGTGGCTCATACCCGTAATCCCAACAC A G RB1 Ensembl:ENSG00000139687 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1373687267 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12174089 RMVar_hsa_circ_40359,RMVar_hsa_circ_39893,RMVar_hsa_circ_105953,RMVar_hsa_circ_163317,RMVar_hsa_circ_75365,RMVar_hsa_circ_18923,RMVar_hsa_circ_56206,RMVar_hsa_circ_266621 47402 RMVar_ID_47402 Human_SNP_ID_530014185 A-to-I Human chr13 + 48991431 48991431 48991431 GAACTGGCCTGGGGGCAGTGGCTCATGTTTGTAATCCCAGCTCTTTGGGAGGCTGAGGGGGTTGA GAACTGGCCTGGGGGCAGTGGCTCATGTTTGTGATCCCAGCTCTTTGGGAGGCTGAGGGGGTTGA A G FNDC3A Ensembl:ENSG00000102531 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1333548337 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112505,RMVar_hsa_circ_163332 47403 RMVar_ID_47403 Human_SNP_ID_530023571 A-to-I Human chr13 + 49028296 49028296 49028296 TCTTTATTTTTTAAGAGACAGGGTCTTGCTCTATCACCAGGCTGAAGTGCAGTGGTGCCATTGTA TCTTTATTTTTTAAGAGACAGGGTCTTGCTCTGTCACCAGGCTGAAGTGCAGTGGTGCCATTGTA A G FNDC3A Ensembl:ENSG00000102531 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1308151262 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112505,RMVar_hsa_circ_334012,RMVar_hsa_circ_163332,RMVar_hsa_circ_367408,RMVar_hsa_circ_285133,RMVar_hsa_circ_322167,RMVar_hsa_circ_80469,RMVar_hsa_circ_163334,RMVar_hsa_circ_163335,RMVar_hsa_circ_163333 47404 RMVar_ID_47404 Human_SNP_ID_530023583 A-to-I Human chr13 + 49028353 49028353 49028353 CCATTGTAGCCCTGAGCTCAAGTGATTCTCCTACCTCAGCCTCCTAAGTAGCTGGGACTCCAGGT CCATTGTAGCCCTGAGCTCAAGTGATTCTCCTGCCTCAGCCTCCTAAGTAGCTGGGACTCCAGGT A G FNDC3A Ensembl:ENSG00000102531 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1023952452 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112505,RMVar_hsa_circ_334012,RMVar_hsa_circ_163332,RMVar_hsa_circ_367408,RMVar_hsa_circ_285133,RMVar_hsa_circ_322167,RMVar_hsa_circ_80469,RMVar_hsa_circ_163334,RMVar_hsa_circ_163335,RMVar_hsa_circ_163333 47405 RMVar_ID_47405 Human_SNP_ID_530026586 A-to-I Human chr13 + 49041712 49041712 49041712 GGGCACCTGTAATCCCAGCTACTCGGGAGGGTAAGGCAGGAGATTTGCTTGAACCCAGGATGCGG GGGCACCTGTAATCCCAGCTACTCGGGAGGGTGAGGCAGGAGATTTGCTTGAACCCAGGATGCGG A G FNDC3A Ensembl:ENSG00000102531 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs577389072 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112505,RMVar_hsa_circ_334012,RMVar_hsa_circ_163332,RMVar_hsa_circ_367408,RMVar_hsa_circ_285133,RMVar_hsa_circ_322167,RMVar_hsa_circ_80469,RMVar_hsa_circ_163334,RMVar_hsa_circ_163335,RMVar_hsa_circ_163333 47406 RMVar_ID_47406 Human_SNP_ID_530026895 A-to-I Human chr13 + 49043019 49043019 49043019 ATTCTGTCACCAAGACTGGAATGCAGTGGTACAATCAAGGCTCACTTCAGCCTTGACCTCCTGGG ATTCTGTCACCAAGACTGGAATGCAGTGGTACCATCAAGGCTCACTTCAGCCTTGACCTCCTGGG A C FNDC3A Ensembl:ENSG00000102531 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs550881085 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112505,RMVar_hsa_circ_334012,RMVar_hsa_circ_163332,RMVar_hsa_circ_367408,RMVar_hsa_circ_285133,RMVar_hsa_circ_322167,RMVar_hsa_circ_80469,RMVar_hsa_circ_163334,RMVar_hsa_circ_163335,RMVar_hsa_circ_163333 47407 RMVar_ID_47407 Human_SNP_ID_530027545 A-to-I Human chr13 + 49045405 49045405 49045405 CAAACTCCTGACCTCAAGGATACTCCTGCCTCAGCCTCCCAAAGTGCTGGGATTGCAGGTGTGAG CAAACTCCTGACCTCAAGGATACTCCTGCCTCGGCCTCCCAAAGTGCTGGGATTGCAGGTGTGAG A G FNDC3A Ensembl:ENSG00000102531 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1009277590 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112505,RMVar_hsa_circ_334012,RMVar_hsa_circ_163332,RMVar_hsa_circ_367408,RMVar_hsa_circ_285133,RMVar_hsa_circ_322167,RMVar_hsa_circ_80469,RMVar_hsa_circ_163334,RMVar_hsa_circ_163335,RMVar_hsa_circ_163333 47408 RMVar_ID_47408 Human_SNP_ID_530063526 A-to-I Human chr13 + 49193335 49193335 49193335 CAGGCTGGAGAGCAGGGGTATGATCATGGCTCACTGCAACCTCAACCTCCCAGGCTTAAGCGATC CAGGCTGGAGAGCAGGGGTATGATCATGGCTCGCTGCAACCTCAACCTCCCAGGCTTAAGCGATC A G FNDC3A Ensembl:ENSG00000102531 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1412324602 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_163347,RMVar_hsa_circ_80469,RMVar_hsa_circ_163333,RMVar_hsa_circ_79714,RMVar_hsa_circ_163342,RMVar_hsa_circ_347548,RMVar_hsa_circ_163358,RMVar_hsa_circ_24456,RMVar_hsa_circ_19744,RMVar_hsa_circ_294365,RMVar_hsa_circ_163356,RMVar_hsa_circ_285811 47409 RMVar_ID_47409 Human_SNP_ID_530063547 A-to-I Human chr13 + 49193418 49193418 49193418 GAGTAGCAGGGACTATAGGTGCACACCACCATACCAGGCTGATTTTTTACTTTTTTATAGAGATG GAGTAGCAGGGACTATAGGTGCACACCACCATGCCAGGCTGATTTTTTACTTTTTTATAGAGATG A G FNDC3A Ensembl:ENSG00000102531 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs141925413 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_163347,RMVar_hsa_circ_80469,RMVar_hsa_circ_163333,RMVar_hsa_circ_79714,RMVar_hsa_circ_163342,RMVar_hsa_circ_347548,RMVar_hsa_circ_163358,RMVar_hsa_circ_24456,RMVar_hsa_circ_19744,RMVar_hsa_circ_294365,RMVar_hsa_circ_163356,RMVar_hsa_circ_285811 47410 RMVar_ID_47410 Human_SNP_ID_530063553 A-to-I Human chr13 + 49193442 49193442 49193442 ACCACCATACCAGGCTGATTTTTTACTTTTTTATAGAGATGGGGGTCCCCTTATGTTTCCCAGGT ACCACCATACCAGGCTGATTTTTTACTTTTTTGTAGAGATGGGGGTCCCCTTATGTTTCCCAGGT A G FNDC3A Ensembl:ENSG00000102531 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4942805 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_163347,RMVar_hsa_circ_80469,RMVar_hsa_circ_163333,RMVar_hsa_circ_79714,RMVar_hsa_circ_163342,RMVar_hsa_circ_347548,RMVar_hsa_circ_163358,RMVar_hsa_circ_24456,RMVar_hsa_circ_19744,RMVar_hsa_circ_294365,RMVar_hsa_circ_163356,RMVar_hsa_circ_285811 47411 RMVar_ID_47411 Human_SNP_ID_530063554 A-to-I Human chr13 + 49193442 49193442 49193442 ACCACCATACCAGGCTGATTTTTTACTTTTTTATAGAGATGGGGGTCCCCTTATGTTTCCCAGGT ACCACCATACCAGGCTGATTTTTTACTTTTTTTTAGAGATGGGGGTCCCCTTATGTTTCCCAGGT A T FNDC3A Ensembl:ENSG00000102531 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4942805 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_163347,RMVar_hsa_circ_80469,RMVar_hsa_circ_163333,RMVar_hsa_circ_79714,RMVar_hsa_circ_163342,RMVar_hsa_circ_347548,RMVar_hsa_circ_163358,RMVar_hsa_circ_24456,RMVar_hsa_circ_19744,RMVar_hsa_circ_294365,RMVar_hsa_circ_163356,RMVar_hsa_circ_285811 47412 RMVar_ID_47412 Human_SNP_ID_530064777 A-to-I Human chr13 + 49198654 49198654 49198654 ATATACATTTCTGTAACTATTAGAAGTAGGCCAGGTGTGGTGGCTGACACCTGTAATCTCAGCAC ATATACATTTCTGTAACTATTAGAAGTAGGCCCGGTGTGGTGGCTGACACCTGTAATCTCAGCAC A C FNDC3A Ensembl:ENSG00000102531 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1418181231 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_163356,RMVar_hsa_circ_285811,RMVar_hsa_circ_23746,RMVar_hsa_circ_359029 47413 RMVar_ID_47413 Human_SNP_ID_530066920 A-to-I Human chr13 + 49208383 49208383 49208383 CTGCTGCTTCTCCCATAACTGCTGCCACCACCATCAGAATTCATAATCAAACCTAACCTTTTTGT CTGCTGCTTCTCCCATAACTGCTGCCACCACCGTCAGAATTCATAATCAAACCTAACCTTTTTGT A G FNDC3A Ensembl:ENSG00000102531 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs568650781 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17360001 47414 RMVar_ID_47414 Human_SNP_ID_530080339 A-to-I Human chr13 + 49268419 49268413 49268420 GCAGTGGTTCATGCCTGTAATTGCAACACTTTAGAAGGCTGAGACAGGAGGATCGCTTGAGCTCA GCAGTGGTTCATGCCTGTAATTGCAAC_______AAGGCTGAGACAGGAGGATCGCTTGAGCTCA CACTTTAG C CDADC1 Ensembl:ENSG00000102543 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1241930858 Functional Loss DEL dbSNP153 28..34 33 - - - RMVar_hsa_circ_163360,RMVar_hsa_circ_287804,RMVar_hsa_circ_163361,RMVar_hsa_circ_73294,RMVar_hsa_circ_267336 47415 RMVar_ID_47415 Human_SNP_ID_530080355 A-to-I Human chr13 + 49268459 49268459 49268459 GAGACAGGAGGATCGCTTGAGCTCAGGAGTTCAAGACCAGCGTGGGCAACATAGCAAGACCTCGA GAGACAGGAGGATCGCTTGAGCTCAGGAGTTCGAGACCAGCGTGGGCAACATAGCAAGACCTCGA A G CDADC1 Ensembl:ENSG00000102543 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1299872464 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_163360,RMVar_hsa_circ_287804,RMVar_hsa_circ_163361,RMVar_hsa_circ_73294,RMVar_hsa_circ_267336 47416 RMVar_ID_47416 Human_SNP_ID_530116417 A-to-I Human chr13 - 49427523 49427523 49427523 CACCACGCCCAGCTAATTCTTTTATTTCTTGTAGAGATATGGTCTTACTGTGTTGCCCAGGGTGG CACCACGCCCAGCTAATTCTTTTATTTCTTGTGGAGATATGGTCTTACTGTGTTGCCCAGGGTGG T C CAB39L Ensembl:ENSG00000102547 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs970470996 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35938,RMVar_hsa_circ_67723,RMVar_hsa_circ_21747,RMVar_hsa_circ_345364 47417 RMVar_ID_47417 Human_SNP_ID_530116435 A-to-I Human chr13 - 49427627 49427627 49427627 TGGAGTGCAGTGATGCTATCACAGCTCACTGCAGACTTGACCTCCTGGGCTAAAGCAGTCTTCCC TGGAGTGCAGTGATGCTATCACAGCTCACTGCGGACTTGACCTCCTGGGCTAAAGCAGTCTTCCC T C CAB39L Ensembl:ENSG00000102547 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1471468437 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35938,RMVar_hsa_circ_67723,RMVar_hsa_circ_21747,RMVar_hsa_circ_345364 47418 RMVar_ID_47418 Human_SNP_ID_530125351 A-to-I Human chr13 + 49464959 49464959 49464959 GTGGTGGTGTGTGCCTGTGATTCCAGGTACTCAAGAGGCTGCAGTGGGAGGATCGCTCGAGCCCA GTGGTGGTGTGTGCCTGTGATTCCAGGTACTCCAGAGGCTGCAGTGGGAGGATCGCTCGAGCCCA A C SETDB2 Ensembl:ENSG00000136169 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1052896841 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2756,RMVar_hsa_circ_102111,RMVar_hsa_circ_163370,RMVar_hsa_circ_266810,RMVar_hsa_circ_302348,RMVar_hsa_circ_362472,RMVar_hsa_circ_264905,RMVar_hsa_circ_319922,RMVar_hsa_circ_293406,RMVar_hsa_circ_65228,RMVar_hsa_circ_58655,RMVar_hsa_circ_75447,RMVar_hsa_circ_163374,RMVar_hsa_circ_163376,RMVar_hsa_circ_163377,RMVar_hsa_circ_163375,RMVar_hsa_circ_163373,RMVar_hsa_circ_330573,RMVar_hsa_circ_163380 47419 RMVar_ID_47419 Human_SNP_ID_530125359 A-to-I Human chr13 + 49465007 49465007 49465007 AGGATCGCTCGAGCCCAGGAAATCAAGTCTGCAGTGAGCTGGGATCACACTACTGTACTCCAACC AGGATCGCTCGAGCCCAGGAAATCAAGTCTGCGGTGAGCTGGGATCACACTACTGTACTCCAACC A G SETDB2 Ensembl:ENSG00000136169 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1397952750 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6290378 RMVar_hsa_circ_2756,RMVar_hsa_circ_102111,RMVar_hsa_circ_163370,RMVar_hsa_circ_266810,RMVar_hsa_circ_302348,RMVar_hsa_circ_362472,RMVar_hsa_circ_264905,RMVar_hsa_circ_319922,RMVar_hsa_circ_293406,RMVar_hsa_circ_65228,RMVar_hsa_circ_58655,RMVar_hsa_circ_75447,RMVar_hsa_circ_163374,RMVar_hsa_circ_163376,RMVar_hsa_circ_163377,RMVar_hsa_circ_163375,RMVar_hsa_circ_163373,RMVar_hsa_circ_330573,RMVar_hsa_circ_163380 47420 RMVar_ID_47420 Human_SNP_ID_530146679 A-to-I Human chr13 - 49550839 49550839 49550839 CCTCGGCCTCCCAAAGTGCTGGGATTATAGGCATGAGCCCCACCGTGCCTGGCCTATGCAAAAGT CCTCGGCCTCCCAAAGTGCTGGGATTATAGGCCTGAGCCCCACCGTGCCTGGCCTATGCAAAAGT T G RCBTB1 Ensembl:ENSG00000136144 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1458168038 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36743,RMVar_hsa_circ_368491,RMVar_hsa_circ_90451,RMVar_hsa_circ_39865,RMVar_hsa_circ_125005,RMVar_hsa_circ_163393,RMVar_hsa_circ_82730,RMVar_hsa_circ_163394,RMVar_hsa_circ_163396,RMVar_hsa_circ_163395 47421 RMVar_ID_47421 Human_SNP_ID_530175426 A-to-I Human chr13 - 49665339 49665339 49665339 TGAACACGGGAGGCGGAGGTTGCAGCGAGCCAAGATCTGGCCATTGCACTCCAGCCTGGGTGACA TGAACACGGGAGGCGGAGGTTGCAGCGAGCCACGATCTGGCCATTGCACTCCAGCCTGGGTGACA T G EBPL Ensembl:ENSG00000123179 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1374821525 Functional Loss SNV dbSNP153 33..33 33 - - - 47422 RMVar_ID_47422 Human_SNP_ID_530176214 A-to-I Human chr13 - 49668389 49668389 49668389 TTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTAGCCAGGATGGTCTCGATCTCCTGACCT TTTTGTATTTTTAGTAGAGACGGGGTTTCACCTTGTTAGCCAGGATGGTCTCGATCTCCTGACCT T A EBPL Ensembl:ENSG00000123179 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs180838292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_118729 47423 RMVar_ID_47423 Human_SNP_ID_530176215 A-to-I Human chr13 - 49668389 49668389 49668389 TTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTAGCCAGGATGGTCTCGATCTCCTGACCT TTTTGTATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGGTCTCGATCTCCTGACCT T C EBPL Ensembl:ENSG00000123179 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs180838292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_118729 47424 RMVar_ID_47424 Human_SNP_ID_530176217 A-to-I Human chr13 - 49668392 49668392 49668392 TTTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTAGCCAGGATGGTCTCGATCTCCTGA TTTTTTTGTATTTTTAGTAGAGACGGGGTTTCGCCATGTTAGCCAGGATGGTCTCGATCTCCTGA T C EBPL Ensembl:ENSG00000123179 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs184666784 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_118729 47425 RMVar_ID_47425 Human_SNP_ID_530177490 A-to-I Human chr13 - 49673574 49673574 49673574 AAATTAGGTGGGCGTGGTGGTGCATTCCTGTAATCCCAGCTACTTGGGAGGCTAAGGCAAGAGAA AAATTAGGTGGGCGTGGTGGTGCATTCCTGTAGTCCCAGCTACTTGGGAGGCTAAGGCAAGAGAA T C EBPL Ensembl:ENSG00000123179 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs568954394 Functional Loss SNV dbSNP153 33..33 33 - - - 47426 RMVar_ID_47426 Human_SNP_ID_530180827 A-to-I Human chr13 - 49686769 49686769 49686769 GAGAGAATGGCCAGAAGGCAATTGAAAAATGTAAATTGAGTTGGAGAGACAGAGTCAGGGCAGAA GAGAGAATGGCCAGAAGGCAATTGAAAAATGTTAATTGAGTTGGAGAGACAGAGTCAGGGCAGAA T A EBPL Ensembl:ENSG00000123179 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6561552 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5789,GWAS_ID_5790,GWAS_ID_5791,GWAS_ID_5792,GWAS_ID_5793,GWAS_ID_5794 47427 RMVar_ID_47427 Human_SNP_ID_530180828 A-to-I Human chr13 - 49686769 49686769 49686769 GAGAGAATGGCCAGAAGGCAATTGAAAAATGTAAATTGAGTTGGAGAGACAGAGTCAGGGCAGAA GAGAGAATGGCCAGAAGGCAATTGAAAAATGTGAATTGAGTTGGAGAGACAGAGTCAGGGCAGAA T C EBPL Ensembl:ENSG00000123179 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6561552 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5789,GWAS_ID_5790,GWAS_ID_5791,GWAS_ID_5792,GWAS_ID_5793,GWAS_ID_5794 47428 RMVar_ID_47428 Human_SNP_ID_530181244 A-to-I Human chr13 - 49688533 49688533 49688533 TTGTATTTTTTGTAGAGACGGGGTTTCACCATATTAGCCAGGATGGTCTCGATCTCCTGACCTCG TTGTATTTTTTGTAGAGACGGGGTTTCACCATGTTAGCCAGGATGGTCTCGATCTCCTGACCTCG T C EBPL Ensembl:ENSG00000123179 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1303707018 Functional Loss SNV dbSNP153 33..33 33 - - - 47429 RMVar_ID_47429 Human_SNP_ID_530181627 A-to-I Human chr13 - 49690002 49690002 49690002 GGGATTACGGGCGCCCGTCACCACGCCCAGCTAATTTTTGTGTTTTTAGTAGAGATGAGGTTTCA GGGATTACGGGCGCCCGTCACCACGCCCAGCTGATTTTTGTGTTTTTAGTAGAGATGAGGTTTCA T C EBPL Ensembl:ENSG00000123179 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1193445040 Functional Loss SNV dbSNP153 33..33 33 - - - 47430 RMVar_ID_47430 Human_SNP_ID_530181638 A-to-I Human chr13 - 49690038 49690038 49690038 TAAAGCTATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACGGGCGCCCGTCACCACGCCCA TAAAGCTATTCTCCTGCCTCAGCCTCCCGAGTGGCTGGGATTACGGGCGCCCGTCACCACGCCCA T C EBPL Ensembl:ENSG00000123179 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs375458380 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25055272 47431 RMVar_ID_47431 Human_SNP_ID_530184361 A-to-I Human chr13 - 49701335 49701335 49701335 CCTCCATCATTGTCCTCCACAAACATATTTTCATATTCTTTATGTGGAAGAATAGATTTTAAAGT CCTCCATCATTGTCCTCCACAAACATATTTTCGTATTCTTTATGTGGAAGAATAGATTTTAAAGT T C KPNA3 Ensembl:ENSG00000102753 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs756027747 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4271954,Human_RBP_ID_6290662,Human_RBP_ID_17245079,Human_RBP_ID_17360022,Human_RBP_ID_17476981,Human_RBP_ID_17686390,Human_RBP_ID_17839389,Human_RBP_ID_27428189,Human_RBP_ID_27640265 Human_miRNA_ID_2140133 RMVar_hsa_circ_123685,RMVar_hsa_circ_163403,RMVar_hsa_circ_77144,RMVar_hsa_circ_163402 47432 RMVar_ID_47432 Human_SNP_ID_530190704 A-to-I Human chr13 - 49725719 49725719 49725719 GAATCACTTGAACCCCAGAGGCAGAGATTGCAATGAGTCAAGATGGCGCCACTGCACTCCCGCCT GAATCACTTGAACCCCAGAGGCAGAGATTGCAGTGAGTCAAGATGGCGCCACTGCACTCCCGCCT T C KPNA3 Ensembl:ENSG00000102753 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs964161274 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11679,RMVar_hsa_circ_163403,RMVar_hsa_circ_77144,RMVar_hsa_circ_126577,RMVar_hsa_circ_20643,RMVar_hsa_circ_276531,RMVar_hsa_circ_163410,RMVar_hsa_circ_96101,RMVar_hsa_circ_163411,RMVar_hsa_circ_163409,RMVar_hsa_circ_317931,RMVar_hsa_circ_49037,RMVar_hsa_circ_163417,RMVar_hsa_circ_163416,RMVar_hsa_circ_283035,RMVar_hsa_circ_296058,RMVar_hsa_circ_163418 47433 RMVar_ID_47433 Human_SNP_ID_530192175 A-to-I Human chr13 - 49731053 49731053 49731053 AAATTCGGCTGGGTGCAGTGGCTCACACCTGTAGTCTCAGCACTTTGGGAGGCTGAGGCAGGTGG AAATTCGGCTGGGTGCAGTGGCTCACACCTGTGGTCTCAGCACTTTGGGAGGCTGAGGCAGGTGG T C KPNA3 Ensembl:ENSG00000102753 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1299764262 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11679,RMVar_hsa_circ_163403,RMVar_hsa_circ_77144,RMVar_hsa_circ_126577,RMVar_hsa_circ_20643,RMVar_hsa_circ_276531,RMVar_hsa_circ_163410,RMVar_hsa_circ_96101,RMVar_hsa_circ_163411,RMVar_hsa_circ_163409,RMVar_hsa_circ_317931,RMVar_hsa_circ_49037,RMVar_hsa_circ_163417,RMVar_hsa_circ_163416,RMVar_hsa_circ_283035,RMVar_hsa_circ_296058,RMVar_hsa_circ_163418 47434 RMVar_ID_47434 Human_SNP_ID_530195231 A-to-I Human chr13 - 49742340 49742340 49742340 CATTTTTGGTCCTACTACAAGTATTTTCAGAAATCGAACCATAGTAACTGGAAAGGAAATAATGT CATTTTTGGTCCTACTACAAGTATTTTCAGAAGTCGAACCATAGTAACTGGAAAGGAAATAATGT T C KPNA3 Ensembl:ENSG00000102753 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs777583692 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_163403,RMVar_hsa_circ_77144,RMVar_hsa_circ_317931,RMVar_hsa_circ_283035,RMVar_hsa_circ_163418,RMVar_hsa_circ_163419,RMVar_hsa_circ_329646 47435 RMVar_ID_47435 Human_SNP_ID_530203211 A-to-I Human chr13 - 49774011 49774011 49774011 GTCCCAGCTACTTGGGAGGTTGAGGTGGGAGGATCACCTGAGCCTGGGAGGTTGAGGCTGCAGCG GTCCCAGCTACTTGGGAGGTTGAGGTGGGAGGGTCACCTGAGCCTGGGAGGTTGAGGCTGCAGCG T C KPNA3 Ensembl:ENSG00000102753 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs938185436 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_163403,RMVar_hsa_circ_77144 47436 RMVar_ID_47436 Human_SNP_ID_530203771 A-to-I Human chr13 - 49776202 49776202 49776202 TAAAGTTCTGTAGGGGTACAGCCTGGCGTGGTAGCTCATGCATATAATCCCAGCACTTTGGGAGG TAAAGTTCTGTAGGGGTACAGCCTGGCGTGGTGGCTCATGCATATAATCCCAGCACTTTGGGAGG T C KPNA3 Ensembl:ENSG00000102753 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1303481439 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12177689 RMVar_hsa_circ_163403,RMVar_hsa_circ_77144 47437 RMVar_ID_47437 Human_SNP_ID_530205228 A-to-I Human chr13 - 49782686 49782686 49782686 TTTGTAGAGACAGGGTTTCGCCGTGTTGTCCAAGCTGGTCTCAAACTCTTAGGCTCAAGTGATTC TTTGTAGAGACAGGGTTTCGCCGTGTTGTCCACGCTGGTCTCAAACTCTTAGGCTCAAGTGATTC T G KPNA3 Ensembl:ENSG00000102753 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1314315714 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12177783 RMVar_hsa_circ_163403,RMVar_hsa_circ_77144 47438 RMVar_ID_47438 Human_SNP_ID_530238161 A-to-I Human chr13 - 49913157 49913157 49913157 TCAGCCTCCCAAAGTGCTGGAATTATAGGCGTAAGCCACCACACCCAGCCAGAAAGTGGTTCTCA TCAGCCTCCCAAAGTGCTGGAATTATAGGCGTGAGCCACCACACCCAGCCAGAAAGTGGTTCTCA T C SPRYD7 Ensembl:ENSG00000123178 Protein coding 3'UTR GSE38233;GSE100210;GSE112787 cultured B-cells;HepG2 cell line;293 Flip-In T-REx cells,empty vector - 24183664,29129909,29967493 RNA-Seq:(High) rs1009473123 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26426675 47439 RMVar_ID_47439 Human_SNP_ID_530238162 A-to-I Human chr13 - 49913157 49913157 49913157 TCAGCCTCCCAAAGTGCTGGAATTATAGGCGTAAGCCACCACACCCAGCCAGAAAGTGGTTCTCA TCAGCCTCCCAAAGTGCTGGAATTATAGGCGTCAGCCACCACACCCAGCCAGAAAGTGGTTCTCA T G SPRYD7 Ensembl:ENSG00000123178 Protein coding 3'UTR GSE38233;GSE100210;GSE112787 cultured B-cells;HepG2 cell line;293 Flip-In T-REx cells,empty vector - 24183664,29129909,29967493 RNA-Seq:(High) rs1009473123 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26426675 47440 RMVar_ID_47440 Human_SNP_ID_530238169 A-to-I Human chr13 - 49913168 49913168 49913168 ATCCACCTCCCTCAGCCTCCCAAAGTGCTGGAATTATAGGCGTAAGCCACCACACCCAGCCAGAA ATCCACCTCCCTCAGCCTCCCAAAGTGCTGGAGTTATAGGCGTAAGCCACCACACCCAGCCAGAA T C SPRYD7 Ensembl:ENSG00000123178 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1279052656 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26426675 47441 RMVar_ID_47441 Human_SNP_ID_530238172 A-to-I Human chr13 - 49913179 49913179 49913179 CTGACCTCATGATCCACCTCCCTCAGCCTCCCAAAGTGCTGGAATTATAGGCGTAAGCCACCACA CTGACCTCATGATCCACCTCCCTCAGCCTCCCGAAGTGCTGGAATTATAGGCGTAAGCCACCACA T C SPRYD7 Ensembl:ENSG00000123178 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1224517692 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26426675 47442 RMVar_ID_47442 Human_SNP_ID_530238185 A-to-I Human chr13 - 49913217 49913217 49913217 TGGGGTTTCACCATGTTGTCCAGGCTGGTCTCAAACTCCTGACCTCATGATCCACCTCCCTCAGC TGGGGTTTCACCATGTTGTCCAGGCTGGTCTCGAACTCCTGACCTCATGATCCACCTCCCTCAGC T C SPRYD7 Ensembl:ENSG00000123178 Protein coding 3'UTR GSE47997;GSE38233;GSE112787 K562 cells&HepG2 cells;cultured B-cells;293 Flip-In T-REx cells,empty vector - 23474544,24183664,29967493 RNA-Seq:(High) rs1474979688 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26426675 47443 RMVar_ID_47443 Human_SNP_ID_530238346 A-to-I Human chr13 - 49913761 49913761 49913761 AGCACTTTGGGAGGCTGAGGCGGGAGGATCACAAGGTCAGGAGATCGAGACCATCGTGGCTAACA AGCACTTTGGGAGGCTGAGGCGGGAGGATCACGAGGTCAGGAGATCGAGACCATCGTGGCTAACA T C SPRYD7 Ensembl:ENSG00000123178 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1306560037 Functional Loss SNV dbSNP153 33..33 33 - - - 47444 RMVar_ID_47444 Human_SNP_ID_530238358 A-to-I Human chr13 - 49913805 49913805 49913805 CATAGGCACTTGCGCCAGGCGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGC CATAGGCACTTGCGCCAGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGC T C SPRYD7 Ensembl:ENSG00000123178 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs3203165 Functional Loss SNV dbSNP153 33..33 33 - - - 47445 RMVar_ID_47445 Human_SNP_ID_530238368 A-to-I Human chr13 - 49913821 49913821 49913821 ATAACACCTTAATAATCATAGGCACTTGCGCCAGGCGCGGTGGCTCACACCTGTAATCCCAGCAC ATAACACCTTAATAATCATAGGCACTTGCGCCGGGCGCGGTGGCTCACACCTGTAATCCCAGCAC T C SPRYD7 Ensembl:ENSG00000123178 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1378645986 Functional Loss SNV dbSNP153 33..33 33 - - - 47446 RMVar_ID_47446 Human_SNP_ID_530239630 A-to-I Human chr13 - 49919605 49919605 49919605 CTCGTGCCTCAGCCTCCAGAGTAGCTGGGATTACAGGTGTGTATCACCACACCCAGCTAACTTTT CTCGTGCCTCAGCCTCCAGAGTAGCTGGGATTCCAGGTGTGTATCACCACACCCAGCTAACTTTT T G SPRYD7 Ensembl:ENSG00000123178 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs895534548 Functional Loss SNV dbSNP153 33..33 33 - - - 47447 RMVar_ID_47447 Human_SNP_ID_530255511 A-to-I Human chr13 - 49991351 49991343 49991351 TTTGTATTTTTTTGTAGAGATGGTGTTTTGCCATGTTGCCTAGGCTAGTCTCAAACTCACAGACT TTTGTATTTTTTTGTAGAGATGGTGTTTTGCC________TAGGCTAGTCTCAAACTCACAGACT AGGCAACAT A DLEU2 Ensembl:ENSG00000231607 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1377427670 Functional Loss DEL dbSNP153 33..40 33 - - - RMVar_hsa_circ_57304 47448 RMVar_ID_47448 Human_SNP_ID_530255514 A-to-I Human chr13 - 49991351 49991351 49991351 TTTGTATTTTTTTGTAGAGATGGTGTTTTGCCATGTTGCCTAGGCTAGTCTCAAACTCACAGACT TTTGTATTTTTTTGTAGAGATGGTGTTTTGCCGTGTTGCCTAGGCTAGTCTCAAACTCACAGACT T C DLEU2 Ensembl:ENSG00000231607 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1403157604 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57304 47449 RMVar_ID_47449 Human_SNP_ID_530256302 A-to-I Human chr13 - 49994935 49994935 49994935 TCACTACAGCCTCAAGCCCCTGGGCCCAAGTTATCCTCCTCCCTTAGCCTCCCAAGTAGCTGGGA TCACTACAGCCTCAAGCCCCTGGGCCCAAGTTTTCCTCCTCCCTTAGCCTCCCAAGTAGCTGGGA T A DLEU2 Ensembl:ENSG00000231607 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1420786951 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57697,RMVar_hsa_circ_320802,RMVar_hsa_circ_57304,RMVar_hsa_circ_314598,RMVar_hsa_circ_163427,RMVar_hsa_circ_26225,RMVar_hsa_circ_163428 47450 RMVar_ID_47450 Human_SNP_ID_530256311 A-to-I Human chr13 - 49994962 49994962 49994962 GCTGGAGTGCAGTAGCATGATCATGGCTCACTACAGCCTCAAGCCCCTGGGCCCAAGTTATCCTC GCTGGAGTGCAGTAGCATGATCATGGCTCACTGCAGCCTCAAGCCCCTGGGCCCAAGTTATCCTC T C DLEU2 Ensembl:ENSG00000231607 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1321675638 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57697,RMVar_hsa_circ_320802,RMVar_hsa_circ_57304,RMVar_hsa_circ_314598,RMVar_hsa_circ_163427,RMVar_hsa_circ_26225,RMVar_hsa_circ_163428 47451 RMVar_ID_47451 Human_SNP_ID_530259527 A-to-I Human chr13 + 50005563 50005563 50005563 TGGCATGGTTGTAGGCGCGTGTAATCCCAGCTACTCGGGGAGACTAAGGCAGGAGAATCACTTGA TGGCATGGTTGTAGGCGCGTGTAATCCCAGCTGCTCGGGGAGACTAAGGCAGGAGAATCACTTGA A G TRIM13 Ensembl:ENSG00000204977 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs564622439 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_163429,RMVar_hsa_circ_119200 47452 RMVar_ID_47452 Human_SNP_ID_530259528 A-to-I Human chr13 + 50005563 50005563 50005563 TGGCATGGTTGTAGGCGCGTGTAATCCCAGCTACTCGGGGAGACTAAGGCAGGAGAATCACTTGA TGGCATGGTTGTAGGCGCGTGTAATCCCAGCTTCTCGGGGAGACTAAGGCAGGAGAATCACTTGA A T TRIM13 Ensembl:ENSG00000204977 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs564622439 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_163429,RMVar_hsa_circ_119200 47453 RMVar_ID_47453 Human_SNP_ID_530259649 A-to-I Human chr13 + 50005926 50005926 50005926 TTTAGTAGAGACGGGGTTTCTCCATGTGGGCCAGGCTGGTCTCGAACTCCCGACCTCATCTGCCC TTTAGTAGAGACGGGGTTTCTCCATGTGGGCCGGGCTGGTCTCGAACTCCCGACCTCATCTGCCC A G TRIM13 Ensembl:ENSG00000204977 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1403490206 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12179400,Human_RBP_ID_25055861 RMVar_hsa_circ_163429,RMVar_hsa_circ_119200 47454 RMVar_ID_47454 Human_SNP_ID_530264881 A-to-I Human chr13 - 50023784 50023784 50023784 AGCCAGGCATGGTGGCATGCACTTGCAGTCCCAGGTACTCAGGAGGCTGAGGCTAGAGGATAGCT AGCCAGGCATGGTGGCATGCACTTGCAGTCCCGGGTACTCAGGAGGCTGAGGCTAGAGGATAGCT T C DLEU2 Ensembl:ENSG00000231607 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1047305555 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12180042 RMVar_hsa_circ_57697,RMVar_hsa_circ_320802,RMVar_hsa_circ_57304,RMVar_hsa_circ_314598,RMVar_hsa_circ_163428,RMVar_hsa_circ_309616,RMVar_hsa_circ_351035,RMVar_hsa_circ_163430,RMVar_hsa_circ_163431 47455 RMVar_ID_47455 Human_SNP_ID_530264916 A-to-I Human chr13 - 50023919 50023919 50023919 ACCATGTGCAGTGGCACACGCCTGTAATCCCAACACTTTGGGAGGGTGAGGTGGAAGGATTGCTT ACCATGTGCAGTGGCACACGCCTGTAATCCCAGCACTTTGGGAGGGTGAGGTGGAAGGATTGCTT T C DLEU2 Ensembl:ENSG00000231607 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1414382819 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57697,RMVar_hsa_circ_320802,RMVar_hsa_circ_57304,RMVar_hsa_circ_314598,RMVar_hsa_circ_163428,RMVar_hsa_circ_309616,RMVar_hsa_circ_351035,RMVar_hsa_circ_163430,RMVar_hsa_circ_163431 47456 RMVar_ID_47456 Human_SNP_ID_530265034 A-to-I Human chr13 - 50024516 50024516 50024516 GAGTCTCACTTCTTTGCCCAGGCTGGAGGGCAATGGTGCAATCTCAGCTTACTACAACCTCTGCC GAGTCTCACTTCTTTGCCCAGGCTGGAGGGCAGTGGTGCAATCTCAGCTTACTACAACCTCTGCC T C DLEU2 Ensembl:ENSG00000231607 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs974714639 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3432120,Human_RBP_ID_19868646 RMVar_hsa_circ_57697,RMVar_hsa_circ_320802,RMVar_hsa_circ_57304,RMVar_hsa_circ_314598,RMVar_hsa_circ_163428,RMVar_hsa_circ_309616,RMVar_hsa_circ_351035,RMVar_hsa_circ_163430,RMVar_hsa_circ_163431 47457 RMVar_ID_47457 Human_SNP_ID_530266756 A-to-I Human chr13 - 50033092 50033092 50033092 CACCGCGCCCAGCTAATTTTTGTACATTTAGTAGAGACGGGTTTCGCCATGTTGGCCAGGCTGGC CACCGCGCCCAGCTAATTTTTGTACATTTAGTGGAGACGGGTTTCGCCATGTTGGCCAGGCTGGC T C DLEU2 Ensembl:ENSG00000231607 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1345734001 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6315114,Human_RBP_ID_12180377,Human_RBP_ID_25056205 RMVar_hsa_circ_320802,RMVar_hsa_circ_57304,RMVar_hsa_circ_314598,RMVar_hsa_circ_163428,RMVar_hsa_circ_309616,RMVar_hsa_circ_351035,RMVar_hsa_circ_98867,RMVar_hsa_circ_163430,RMVar_hsa_circ_163431,RMVar_hsa_circ_317345,RMVar_hsa_circ_163437,RMVar_hsa_circ_62823,RMVar_hsa_circ_32027,RMVar_hsa_circ_163438 47458 RMVar_ID_47458 Human_SNP_ID_530268626 A-to-I Human chr13 - 50039795 50039795 50039795 GAGACCCCATCTCTACTAAAAATACAAAAATTAGCCGTGCATGGTGGTGCACGCCTGTAGTCCCT GAGACCCCATCTCTACTAAAAATACAAAAATTGGCCGTGCATGGTGGTGCACGCCTGTAGTCCCT T C DLEU2 Ensembl:ENSG00000231607 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417293453 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12180619 RMVar_hsa_circ_320802,RMVar_hsa_circ_57304,RMVar_hsa_circ_314598,RMVar_hsa_circ_163428,RMVar_hsa_circ_309616,RMVar_hsa_circ_351035,RMVar_hsa_circ_98867,RMVar_hsa_circ_163430,RMVar_hsa_circ_163431,RMVar_hsa_circ_317345,RMVar_hsa_circ_163437,RMVar_hsa_circ_62823,RMVar_hsa_circ_32027,RMVar_hsa_circ_163438 47459 RMVar_ID_47459 Human_SNP_ID_530269089 A-to-I Human chr13 - 50042042 50042042 50042042 TATTTTTAGTAGAGACGGTGTTTCACTGTGTTAGCCAGGCTGATCTCAAACTCCTGACCTCGTGA TATTTTTAGTAGAGACGGTGTTTCACTGTGTTGGCCAGGCTGATCTCAAACTCCTGACCTCGTGA T C DLEU2 Ensembl:ENSG00000231607 lincRNA intron GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs763000427 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1084155,Human_RBP_ID_3432205,Human_RBP_ID_25056377 RMVar_hsa_circ_320802,RMVar_hsa_circ_57304,RMVar_hsa_circ_314598,RMVar_hsa_circ_163428,RMVar_hsa_circ_309616,RMVar_hsa_circ_351035,RMVar_hsa_circ_98867,RMVar_hsa_circ_163430,RMVar_hsa_circ_163431,RMVar_hsa_circ_317345,RMVar_hsa_circ_163437,RMVar_hsa_circ_62823,RMVar_hsa_circ_32027,RMVar_hsa_circ_163438 47460 RMVar_ID_47460 Human_SNP_ID_530269099 A-to-I Human chr13 - 50042086 50042086 50042086 AGCTGGGATTACAGGCATCTGCCACCACACCCAGCTAATTTTTGTATTTTTAGTAGAGACGGTGT AGCTGGGATTACAGGCATCTGCCACCACACCCGGCTAATTTTTGTATTTTTAGTAGAGACGGTGT T C DLEU2 Ensembl:ENSG00000231607 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1248822546 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_320802,RMVar_hsa_circ_57304,RMVar_hsa_circ_314598,RMVar_hsa_circ_163428,RMVar_hsa_circ_309616,RMVar_hsa_circ_351035,RMVar_hsa_circ_98867,RMVar_hsa_circ_163430,RMVar_hsa_circ_163431,RMVar_hsa_circ_317345,RMVar_hsa_circ_163437,RMVar_hsa_circ_62823,RMVar_hsa_circ_32027,RMVar_hsa_circ_163438 47461 RMVar_ID_47461 Human_SNP_ID_530270928 A-to-I Human chr13 - 50050150 50050150 50050150 ACTAGAGTGGTGGCAATTTTCTGATATCTTTTAGAGAAAAGGAATTTCATTTCTACATCTGAGAA ACTAGAGTGGTGGCAATTTTCTGATATCTTTTCGAGAAAAGGAATTTCATTTCTACATCTGAGAA T G DLEU2 Ensembl:ENSG00000231607 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1237695315 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39039,RMVar_hsa_circ_32027,RMVar_hsa_circ_282725,RMVar_hsa_circ_305886 47462 RMVar_ID_47462 Human_SNP_ID_530274832 A-to-I Human chr13 - 50065621 50065621 50065621 GGGCGTCGTGGCGGGTGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGGGAATGCCGTGAA GGGCGTCGTGGCGGGTGCCTGTAGTCCCAGCTGCTCAGGAGGCTGAGGCAGGGGAATGCCGTGAA T C DLEU2 Ensembl:ENSG00000231607 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1354728496 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17562012 RMVar_hsa_circ_39039,RMVar_hsa_circ_32027,RMVar_hsa_circ_282725,RMVar_hsa_circ_305886 47463 RMVar_ID_47463 Human_SNP_ID_530589923 A-to-I Human chr13 + 51456139 51456139 51456139 GGTATGTGGACAAGTGGAGGGTGAGCAAGGCAAAGAGGTGCTTTGTTGAGTGACAGAACAGCTCA GGTATGTGGACAAGTGGAGGGTGAGCAAGGCAGAGAGGTGCTTTGTTGAGTGACAGAACAGCTCA A G RPS4XP16,INTS6-AS1 Ensembl:ENSG00000224892,Ensembl:ENSG00000236778 Pseudogene,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1197372741 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17360901 47464 RMVar_ID_47464 Human_SNP_ID_530654127 A-to-I Human chr13 + 51725371 51725369 51725372 CCCCTTGTCATAGTTCCCATTTGGAATCCTGTAATATTTTTACATATTAAAAATACATAAAATTT CCCCTTGTCATAGTTCCCATTTGGAATCCTG___TATTTTTACATATTAAAAATACATAAAATTT GTAA G WDFY2 Ensembl:ENSG00000139668 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1034524716 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_29302,RMVar_hsa_circ_121250,RMVar_hsa_circ_103275,RMVar_hsa_circ_340418,RMVar_hsa_circ_163485,RMVar_hsa_circ_376000,RMVar_hsa_circ_163487,RMVar_hsa_circ_163489,RMVar_hsa_circ_109275,RMVar_hsa_circ_163488,RMVar_hsa_circ_312093,RMVar_hsa_circ_285101,RMVar_hsa_circ_163492,RMVar_hsa_circ_163490,RMVar_hsa_circ_163491,RMVar_hsa_circ_308928,RMVar_hsa_circ_337865,RMVar_hsa_circ_304404,RMVar_hsa_circ_163494,RMVar_hsa_circ_311257,RMVar_hsa_circ_331816,RMVar_hsa_circ_290089,RMVar_hsa_circ_163493 47465 RMVar_ID_47465 Human_SNP_ID_530726390 A-to-I Human chr13 + 52022261 52022261 52022261 ATGGTGGCACACATCTGTAATCCCAGCTTCTCAGGAGGCTGAGGCACGAAAATCACTTGAACCCG ATGGTGGCACACATCTGTAATCCCAGCTTCTCGGGAGGCTGAGGCACGAAAATCACTTGAACCCG A G ALG11 Ensembl:ENSG00000253710 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs772337891 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57514 47466 RMVar_ID_47466 Human_SNP_ID_530726405 A-to-I Human chr13 + 52022307 52022307 52022307 CGAAAATCACTTGAACCCGAGAGGTGGAGGCTACAATAAGCCAAGATCACGCCACTGTACTCCCG CGAAAATCACTTGAACCCGAGAGGTGGAGGCTGCAATAAGCCAAGATCACGCCACTGTACTCCCG A G ALG11 Ensembl:ENSG00000253710 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1395087381 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12260218 RMVar_hsa_circ_57514 47467 RMVar_ID_47467 Human_SNP_ID_530726408 A-to-I Human chr13 + 52022317 52022317 52022317 TTGAACCCGAGAGGTGGAGGCTACAATAAGCCAAGATCACGCCACTGTACTCCCGCCTGGGCGAC TTGAACCCGAGAGGTGGAGGCTACAATAAGCCGAGATCACGCCACTGTACTCCCGCCTGGGCGAC A G ALG11 Ensembl:ENSG00000253710 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs543616842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12187586 RMVar_hsa_circ_57514 47468 RMVar_ID_47468 Human_SNP_ID_530726529 A-to-I Human chr13 + 52022754 52022754 52022754 GAGTTTCATTGTTGTTGCCCAGGCTGGAGTGCAGTGGTGCGATCTTGGCTCACCACAACCTCCGC GAGTTTCATTGTTGTTGCCCAGGCTGGAGTGCGGTGGTGCGATCTTGGCTCACCACAACCTCCGC A G ALG11 Ensembl:ENSG00000253710 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1454614910 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57514 47469 RMVar_ID_47469 Human_SNP_ID_530728856 A-to-I Human chr13 + 52030849 52030849 52030849 GCGCAACATCCACGCAGCAGCTCATCAGGTACAAGTGCTTCCATATCCATTTACCCACCATCGGC GCGCAACATCCACGCAGCAGCTCATCAGGTACCAGTGCTTCCATATCCATTTACCCACCATCGGC A C ALG11,UTP14C Ensembl:ENSG00000253710,Ensembl:ENSG00000253797 Protein coding,Protein coding 3'UTR,CDS GSE100210;GSE107867 HepG2 cell line;ASD brains,frontal_cortex - 29129909,30559470 RNA-Seq:(High) rs772344954 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3433066,Human_RBP_ID_17245141,Human_RBP_ID_17360102 47470 RMVar_ID_47470 Human_SNP_ID_530728857 A-to-I Human chr13 + 52030849 52030849 52030849 GCGCAACATCCACGCAGCAGCTCATCAGGTACAAGTGCTTCCATATCCATTTACCCACCATCGGC GCGCAACATCCACGCAGCAGCTCATCAGGTACGAGTGCTTCCATATCCATTTACCCACCATCGGC A G ALG11,UTP14C Ensembl:ENSG00000253710,Ensembl:ENSG00000253797 Protein coding,Protein coding 3'UTR,CDS GSE100210;GSE107867 HepG2 cell line;ASD brains,frontal_cortex - 29129909,30559470 RNA-Seq:(High) rs772344954 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3433066,Human_RBP_ID_17245141,Human_RBP_ID_17360102 47471 RMVar_ID_47471 Human_SNP_ID_530821793 A-to-I Human chr13 - 52417091 52417091 52417091 TGGCGTCATGGTAATTGAGCTTCAGTCTCACAAGGAAGAGGAAATGGTGGCCTCGGCCCTGGAGA TGGCGTCATGGTAATTGAGCTTCAGTCTCACAGGGAAGAGGAAATGGTGGCCTCGGCCCTGGAGA T C VPS36 Ensembl:ENSG00000136100 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1040812952 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1485502,Human_RBP_ID_1810960,Human_RBP_ID_9367960 Human_Splice_Rec_1468600,Human_Splice_Rec_1468601,Human_Splice_Rec_1468628,Human_Splice_Rec_1468629,Human_Splice_Rec_1468654,Human_Splice_Rec_1468655 RMVar_hsa_circ_21732,RMVar_hsa_circ_91937,RMVar_hsa_circ_108149,RMVar_hsa_circ_57011,RMVar_hsa_circ_163533,RMVar_hsa_circ_163534,RMVar_hsa_circ_318484,RMVar_hsa_circ_346747,RMVar_hsa_circ_126813,RMVar_hsa_circ_47445,RMVar_hsa_circ_163536,RMVar_hsa_circ_163537,RMVar_hsa_circ_163538,RMVar_hsa_circ_163535 47472 RMVar_ID_47472 Human_SNP_ID_530822124 A-to-I Human chr13 - 52418543 52418543 52418543 TTGAGATGGAGTCTCGCACTATCGCCCAGGCTAGAATGCATGGTGCGATCTCGGCTAACTGCAAA TTGAGATGGAGTCTCGCACTATCGCCCAGGCTGGAATGCATGGTGCGATCTCGGCTAACTGCAAA T C VPS36 Ensembl:ENSG00000136100 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1487417255 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12188508 RMVar_hsa_circ_21732,RMVar_hsa_circ_91937,RMVar_hsa_circ_108149,RMVar_hsa_circ_57011,RMVar_hsa_circ_163533,RMVar_hsa_circ_163534,RMVar_hsa_circ_318484,RMVar_hsa_circ_346747,RMVar_hsa_circ_47445,RMVar_hsa_circ_163540,RMVar_hsa_circ_92895,RMVar_hsa_circ_163536,RMVar_hsa_circ_163537,RMVar_hsa_circ_163538,RMVar_hsa_circ_284718,RMVar_hsa_circ_356078,RMVar_hsa_circ_274214,RMVar_hsa_circ_23736,RMVar_hsa_circ_83266,RMVar_hsa_circ_163541,RMVar_hsa_circ_163542,RMVar_hsa_circ_163539 47473 RMVar_ID_47473 Human_SNP_ID_530822662 A-to-I Human chr13 - 52420680 52420680 52420680 GTCACCTCCAGTGTTTATCATTCCTTTGTGTTAGGAACATTCCAATTCCACTTTTGTAGTTACTT GTCACCTCCAGTGTTTATCATTCCTTTGTGTTGGGAACATTCCAATTCCACTTTTGTAGTTACTT T C VPS36 Ensembl:ENSG00000136100 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1242959200 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21732,RMVar_hsa_circ_91937,RMVar_hsa_circ_108149,RMVar_hsa_circ_57011,RMVar_hsa_circ_163533,RMVar_hsa_circ_163534,RMVar_hsa_circ_318484,RMVar_hsa_circ_346747,RMVar_hsa_circ_47445,RMVar_hsa_circ_163540,RMVar_hsa_circ_92895,RMVar_hsa_circ_163536,RMVar_hsa_circ_163537,RMVar_hsa_circ_163538,RMVar_hsa_circ_284718,RMVar_hsa_circ_356078,RMVar_hsa_circ_274214,RMVar_hsa_circ_23736,RMVar_hsa_circ_83266,RMVar_hsa_circ_163541,RMVar_hsa_circ_163542,RMVar_hsa_circ_163539 47474 RMVar_ID_47474 Human_SNP_ID_530822712 A-to-I Human chr13 - 52420895 52420895 52420895 ACTGGTCTTGAACTCCTGACCTAAGGTGATCTACCCACCTTGGCCTCCCAAACAAAGTGCTGGGA ACTGGTCTTGAACTCCTGACCTAAGGTGATCTGCCCACCTTGGCCTCCCAAACAAAGTGCTGGGA T C VPS36 Ensembl:ENSG00000136100 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1333389968 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21732,RMVar_hsa_circ_91937,RMVar_hsa_circ_108149,RMVar_hsa_circ_57011,RMVar_hsa_circ_163533,RMVar_hsa_circ_163534,RMVar_hsa_circ_318484,RMVar_hsa_circ_346747,RMVar_hsa_circ_47445,RMVar_hsa_circ_163540,RMVar_hsa_circ_92895,RMVar_hsa_circ_163536,RMVar_hsa_circ_163537,RMVar_hsa_circ_163538,RMVar_hsa_circ_284718,RMVar_hsa_circ_356078,RMVar_hsa_circ_274214,RMVar_hsa_circ_23736,RMVar_hsa_circ_83266,RMVar_hsa_circ_163541,RMVar_hsa_circ_163542,RMVar_hsa_circ_163539 47475 RMVar_ID_47475 Human_SNP_ID_530822734 A-to-I Human chr13 - 52421012 52421012 52421012 GGTTCAAGCAATTCTTGTGCTTCAGCTTCTCAAGTAGCTGGGATTACAGCCGTGTGCCACCACAC GGTTCAAGCAATTCTTGTGCTTCAGCTTCTCAGGTAGCTGGGATTACAGCCGTGTGCCACCACAC T C VPS36 Ensembl:ENSG00000136100 Protein coding intron GSE38233;GSE107867 cultured B-cells;ASD brains,cerebellum - 24183664,30559470 RNA-Seq:(High) rs1026105700 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21732,RMVar_hsa_circ_91937,RMVar_hsa_circ_108149,RMVar_hsa_circ_57011,RMVar_hsa_circ_163533,RMVar_hsa_circ_163534,RMVar_hsa_circ_318484,RMVar_hsa_circ_346747,RMVar_hsa_circ_47445,RMVar_hsa_circ_163540,RMVar_hsa_circ_92895,RMVar_hsa_circ_163536,RMVar_hsa_circ_163537,RMVar_hsa_circ_163538,RMVar_hsa_circ_284718,RMVar_hsa_circ_356078,RMVar_hsa_circ_274214,RMVar_hsa_circ_23736,RMVar_hsa_circ_83266,RMVar_hsa_circ_163541,RMVar_hsa_circ_163542,RMVar_hsa_circ_163539 47476 RMVar_ID_47476 Human_SNP_ID_530822945 A-to-I Human chr13 - 52421998 52421998 52421998 GGCAACAATGTATTGTATATTTCAAAGTAGCTAGAAGGGAGGACTTGAAATGTTCCTAAAACATA GGCAACAATGTATTGTATATTTCAAAGTAGCTGGAAGGGAGGACTTGAAATGTTCCTAAAACATA T C VPS36 Ensembl:ENSG00000136100 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904389426 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21732,RMVar_hsa_circ_91937,RMVar_hsa_circ_108149,RMVar_hsa_circ_57011,RMVar_hsa_circ_163533,RMVar_hsa_circ_163534,RMVar_hsa_circ_318484,RMVar_hsa_circ_346747,RMVar_hsa_circ_47445,RMVar_hsa_circ_163540,RMVar_hsa_circ_92895,RMVar_hsa_circ_163536,RMVar_hsa_circ_163537,RMVar_hsa_circ_163538,RMVar_hsa_circ_284718,RMVar_hsa_circ_356078,RMVar_hsa_circ_274214,RMVar_hsa_circ_23736,RMVar_hsa_circ_83266,RMVar_hsa_circ_163541,RMVar_hsa_circ_163542,RMVar_hsa_circ_163539 47477 RMVar_ID_47477 Human_SNP_ID_530822994 A-to-I Human chr13 - 52422213 52422213 52422213 AAGTGAAGTAAGCCAGACACAGAAAGACAAATATTGCATGTTCTCACTCATGTGCGAGCTAAAAA AAGTGAAGTAAGCCAGACACAGAAAGACAAATGTTGCATGTTCTCACTCATGTGCGAGCTAAAAA T C VPS36 Ensembl:ENSG00000136100 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1255903081 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21732,RMVar_hsa_circ_91937,RMVar_hsa_circ_108149,RMVar_hsa_circ_57011,RMVar_hsa_circ_163533,RMVar_hsa_circ_163534,RMVar_hsa_circ_318484,RMVar_hsa_circ_346747,RMVar_hsa_circ_47445,RMVar_hsa_circ_163540,RMVar_hsa_circ_92895,RMVar_hsa_circ_163536,RMVar_hsa_circ_163537,RMVar_hsa_circ_163538,RMVar_hsa_circ_284718,RMVar_hsa_circ_356078,RMVar_hsa_circ_274214,RMVar_hsa_circ_23736,RMVar_hsa_circ_83266,RMVar_hsa_circ_163541,RMVar_hsa_circ_163542,RMVar_hsa_circ_163539 47478 RMVar_ID_47478 Human_SNP_ID_530823002 A-to-I Human chr13 - 52422250 52422250 52422250 TTTGCAGCAACATGGAGAAACTGGAAGTCCTTATGTTAAGTGAAGTAAGCCAGACACAGAAAGAC TTTGCAGCAACATGGAGAAACTGGAAGTCCTTTTGTTAAGTGAAGTAAGCCAGACACAGAAAGAC T A VPS36 Ensembl:ENSG00000136100 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1173892050 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21732,RMVar_hsa_circ_91937,RMVar_hsa_circ_108149,RMVar_hsa_circ_57011,RMVar_hsa_circ_163533,RMVar_hsa_circ_163534,RMVar_hsa_circ_318484,RMVar_hsa_circ_346747,RMVar_hsa_circ_47445,RMVar_hsa_circ_163540,RMVar_hsa_circ_92895,RMVar_hsa_circ_163536,RMVar_hsa_circ_163537,RMVar_hsa_circ_163538,RMVar_hsa_circ_284718,RMVar_hsa_circ_356078,RMVar_hsa_circ_274214,RMVar_hsa_circ_23736,RMVar_hsa_circ_83266,RMVar_hsa_circ_163541,RMVar_hsa_circ_163542,RMVar_hsa_circ_163539 47479 RMVar_ID_47479 Human_SNP_ID_530831550 A-to-I Human chr13 + 52457097 52457097 52457097 TTTTGTATTTTAAACAGAGACCGGGTTTCACTATGTTGGCCGGGCTGGTCTTGGACTCCTGACCT TTTTGTATTTTAAACAGAGACCGGGTTTCACTGTGTTGGCCGGGCTGGTCTTGGACTCCTGACCT A G CKAP2 Ensembl:ENSG00000136108 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs150809210 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12189108 RMVar_hsa_circ_58668,RMVar_hsa_circ_358891 47480 RMVar_ID_47480 Human_SNP_ID_530831551 A-to-I Human chr13 + 52457097 52457097 52457097 TTTTGTATTTTAAACAGAGACCGGGTTTCACTATGTTGGCCGGGCTGGTCTTGGACTCCTGACCT TTTTGTATTTTAAACAGAGACCGGGTTTCACTTTGTTGGCCGGGCTGGTCTTGGACTCCTGACCT A T CKAP2 Ensembl:ENSG00000136108 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs150809210 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12189108 RMVar_hsa_circ_58668,RMVar_hsa_circ_358891 47481 RMVar_ID_47481 Human_SNP_ID_530834410 A-to-I Human chr13 + 52466717 52466717 52466717 CAACATGGCTGGGCACAGTAGTGGATACCTATAGTCTCAACTACTTGGGAGGCCAAGGTGGGAGG CAACATGGCTGGGCACAGTAGTGGATACCTATGGTCTCAACTACTTGGGAGGCCAAGGTGGGAGG A G CKAP2 Ensembl:ENSG00000136108 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1292970536 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12189364 RMVar_hsa_circ_357563,RMVar_hsa_circ_58668,RMVar_hsa_circ_347706 47482 RMVar_ID_47482 Human_SNP_ID_530834631 A-to-I Human chr13 + 52467546 52467545 52467547 CCTGGCCAGCATGGTGAAACTCTGCCTCTACTAAAAATACAAAAAATTAGCTGGGCATGGTGGTG CCTGGCCAGCATGGTGAAACTCTGCCTCTACT__AAATACAAAAAATTAGCTGGGCATGGTGGTG TAA T CKAP2 Ensembl:ENSG00000136108 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1278633739 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_357563,RMVar_hsa_circ_58668,RMVar_hsa_circ_347706 47483 RMVar_ID_47483 Human_SNP_ID_530834647 A-to-I Human chr13 + 52467598 52467598 52467598 GGGCATGGTGGTGCCCACCCGTAATCCCAGCTACTCGAGAGGCTGAGGCAAGAGAATCATTTGAA GGGCATGGTGGTGCCCACCCGTAATCCCAGCTGCTCGAGAGGCTGAGGCAAGAGAATCATTTGAA A G CKAP2 Ensembl:ENSG00000136108 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1001451698 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_357563,RMVar_hsa_circ_58668,RMVar_hsa_circ_347706 47484 RMVar_ID_47484 Human_SNP_ID_530834653 A-to-I Human chr13 + 52467615 52467615 52467615 CCCGTAATCCCAGCTACTCGAGAGGCTGAGGCAAGAGAATCATTTGAACCTGGGAGGCTGAGGTT CCCGTAATCCCAGCTACTCGAGAGGCTGAGGCGAGAGAATCATTTGAACCTGGGAGGCTGAGGTT A G CKAP2 Ensembl:ENSG00000136108 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs142823181 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12189394 RMVar_hsa_circ_357563,RMVar_hsa_circ_58668,RMVar_hsa_circ_347706 47485 RMVar_ID_47485 Human_SNP_ID_530870518 A-to-I Human chr13 + 52628332 52628332 52628332 GGGCATTGTGGCATGTGCCGGCAGTTCTAGCTACTTTGGGGGCTAAGGCTGGAGGATGGCTTAAG GGGCATTGTGGCATGTGCCGGCAGTTCTAGCTCCTTTGGGGGCTAAGGCTGGAGGATGGCTTAAG A C MRPS31P4,AL137058.2 Ensembl:ENSG00000250299,Ensembl:ENSG00000273784 Pseudogene,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs148877172 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16683,RMVar_hsa_circ_126778,RMVar_hsa_circ_163560,RMVar_hsa_circ_91174,RMVar_hsa_circ_91616,RMVar_hsa_circ_163561,RMVar_hsa_circ_296738,RMVar_hsa_circ_163563,RMVar_hsa_circ_27734,RMVar_hsa_circ_122428,RMVar_hsa_circ_163565,RMVar_hsa_circ_163564,RMVar_hsa_circ_118922,RMVar_hsa_circ_163562,RMVar_hsa_circ_357936,RMVar_hsa_circ_163567 47486 RMVar_ID_47486 Human_SNP_ID_530870834 A-to-I Human chr13 + 52629799 52629799 52629799 AGAGAAATGACCCACCATCAACGAAAAGAAAGAAAGGCGTAGGCTGGGCATGGTGGCTCACGCCT AGAGAAATGACCCACCATCAACGAAAAGAAAGTAAGGCGTAGGCTGGGCATGGTGGCTCACGCCT A T MRPS31P4,AL137058.2 Ensembl:ENSG00000250299,Ensembl:ENSG00000273784 Pseudogene,lincRNA intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs994685086 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8249118 RMVar_hsa_circ_16683,RMVar_hsa_circ_296738,RMVar_hsa_circ_163563,RMVar_hsa_circ_27734,RMVar_hsa_circ_122428,RMVar_hsa_circ_163564,RMVar_hsa_circ_163562,RMVar_hsa_circ_357936,RMVar_hsa_circ_345949,RMVar_hsa_circ_345086 47487 RMVar_ID_47487 Human_SNP_ID_530870869 A-to-I Human chr13 + 52629937 52629937 52629937 TGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCCGGACGTGGTGGTGAGCTCCTGCAAT TGGTGAAACCCCATCTCTACTAAAAATACAAAGATTAGCCGGACGTGGTGGTGAGCTCCTGCAAT A G MRPS31P4,AL137058.2 Ensembl:ENSG00000250299,Ensembl:ENSG00000273784 Pseudogene,lincRNA intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs991795084 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16683,RMVar_hsa_circ_296738,RMVar_hsa_circ_163563,RMVar_hsa_circ_27734,RMVar_hsa_circ_122428,RMVar_hsa_circ_163564,RMVar_hsa_circ_163562,RMVar_hsa_circ_357936,RMVar_hsa_circ_345949,RMVar_hsa_circ_345086 47488 RMVar_ID_47488 Human_SNP_ID_530870876 A-to-I Human chr13 + 52629967 52629967 52629967 AAAATTAGCCGGACGTGGTGGTGAGCTCCTGCAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA AAAATTAGCCGGACGTGGTGGTGAGCTCCTGCGATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA A G MRPS31P4,AL137058.2 Ensembl:ENSG00000250299,Ensembl:ENSG00000273784 Pseudogene,lincRNA intron,intron GSE38233;GSE100210;GSE100210;GSE107867;GSE107867 cultured B-cells;HepG2 cell line;HepG2 cell line;ASD brains,temporal_cortex;ASD brains,temporal_cortex - 24183664,29129909,29129909,30559470,30559470 RNA-Seq:(High) rs1200306026 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16683,RMVar_hsa_circ_296738,RMVar_hsa_circ_163563,RMVar_hsa_circ_27734,RMVar_hsa_circ_122428,RMVar_hsa_circ_163564,RMVar_hsa_circ_163562,RMVar_hsa_circ_357936,RMVar_hsa_circ_345949,RMVar_hsa_circ_345086 47489 RMVar_ID_47489 Human_SNP_ID_530870983 A-to-I Human chr13 + 52630464 52630464 52630464 GCCCAGCTCATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGTAACTC GCCCAGCTCATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGGTAACTC A G MRPS31P4,AL137058.2 Ensembl:ENSG00000250299,Ensembl:ENSG00000273784 Pseudogene,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1224295588 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16683,RMVar_hsa_circ_296738,RMVar_hsa_circ_163563,RMVar_hsa_circ_27734,RMVar_hsa_circ_122428,RMVar_hsa_circ_163564,RMVar_hsa_circ_163562,RMVar_hsa_circ_357936,RMVar_hsa_circ_345949,RMVar_hsa_circ_345086 47490 RMVar_ID_47490 Human_SNP_ID_530883451 A-to-I Human chr13 + 52681784 52681784 52681784 TTGAGCCCAGGAGTTCAAGGTTGCAGTGAGCTATGATCGTGCCACTACACTTAGCTTGGGCAGCA TTGAGCCCAGGAGTTCAAGGTTGCAGTGAGCTGTGATCGTGCCACTACACTTAGCTTGGGCAGCA A G SUGT1 Ensembl:ENSG00000165416 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1447001711 Functional Loss SNV dbSNP153 33..33 33 - - - 47491 RMVar_ID_47491 Human_SNP_ID_530883630 A-to-I Human chr13 + 52682324 52682324 52682324 GGGCTCAAGTGATCCTTATGCCTCAGCCTCCCAAGTAGATGGGACTACACATCCATGCTGCCATG GGGCTCAAGTGATCCTTATGCCTCAGCCTCCCGAGTAGATGGGACTACACATCCATGCTGCCATG A G SUGT1 Ensembl:ENSG00000165416 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs549443334 Functional Loss SNV dbSNP153 33..33 33 - - - 47492 RMVar_ID_47492 Human_SNP_ID_530883674 A-to-I Human chr13 + 52682469 52682469 52682469 GCAGTCCTTCGGCCTTGGCTTCCTGAAGTGCTAGAGTTACAGGCGTGAGCCACAGCACCTGGCCT GCAGTCCTTCGGCCTTGGCTTCCTGAAGTGCTGGAGTTACAGGCGTGAGCCACAGCACCTGGCCT A G SUGT1 Ensembl:ENSG00000165416 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1053773394 Functional Loss SNV dbSNP153 33..33 33 - - - 47493 RMVar_ID_47493 Human_SNP_ID_530885845 A-to-I Human chr13 + 52691138 52691138 52691138 CCAAGTAGCTGGGACCACAGGCATGCATCACCACGACTGGCTAATTTTTGTATTTTTTTTGTAGA CCAAGTAGCTGGGACCACAGGCATGCATCACCCCGACTGGCTAATTTTTGTATTTTTTTTGTAGA A C SUGT1 Ensembl:ENSG00000165416 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1187987371 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6295731,Human_RBP_ID_12190638 47494 RMVar_ID_47494 Human_SNP_ID_530885852 A-to-I Human chr13 + 52691168 52691168 52691168 CCACGACTGGCTAATTTTTGTATTTTTTTTGTAGAACCGGGTTTCACCATGTGCCCAGGCTGGTC CCACGACTGGCTAATTTTTGTATTTTTTTTGTGGAACCGGGTTTCACCATGTGCCCAGGCTGGTC A G SUGT1 Ensembl:ENSG00000165416 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947977549 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12190638,Human_RBP_ID_25059595 47495 RMVar_ID_47495 Human_SNP_ID_154584595 A-to-I Human chr3 + 135925970 135925970 135925970 AGAGACAAATATCTGGGGCCTGCAGTTCTTATACAGGCCTATCACTGGATGATTGACTCCAGAGA AGAGACAAATATCTGGGGCCTGCAGTTCTTATGCAGGCCTATCACTGGATGATTGACTCCAGAGA A G AC092989.1 Ensembl:ENSG00000242222 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs576055885 Functional Loss SNV dbSNP153 33..33 33 - - - 47496 RMVar_ID_47496 Human_SNP_ID_154645267 A-to-I Human chr3 - 136164936 136164936 136164936 CTGGGAGATGGAGGTTGCGGTGAGCCAAGATCACGCCACTGCACTCCAGGTGGGCAACAGAGCGA CTGGGAGATGGAGGTTGCGGTGAGCCAAGATCGCGCCACTGCACTCCAGGTGGGCAACAGAGCGA T C MSL2 Ensembl:ENSG00000174579 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1272644039 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25766632 47497 RMVar_ID_47497 Human_SNP_ID_154646754 A-to-I Human chr3 - 136169491 136169491 136169491 TGAGCCCAGATTATGCCACTCCACTGCAGCCTAGGTGACAGAGTGAGACTGCGTCTCAAAAAAAA TGAGCCCAGATTATGCCACTCCACTGCAGCCTGGGTGACAGAGTGAGACTGCGTCTCAAAAAAAA T C MSL2 Ensembl:ENSG00000174579 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs945057406 Functional Loss SNV dbSNP153 33..33 33 - - - 47498 RMVar_ID_47498 Human_SNP_ID_154651220 A-to-I Human chr3 - 136183587 136183587 136183587 AAAACCCTGCCTCTACAACAAATACAAAAATTAGCTGGACATGGTTGGTGCGTGCCTGTAGTCAC AAAACCCTGCCTCTACAACAAATACAAAAATTGGCTGGACATGGTTGGTGCGTGCCTGTAGTCAC T C MSL2 Ensembl:ENSG00000174579 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1464597599 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14633776 47499 RMVar_ID_47499 Human_SNP_ID_154651432 A-to-I Human chr3 - 136184209 136184209 136184209 TCACTGCACCCTCCGCCTCCCGGGTTCGAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGA TCACTGCACCCTCCGCCTCCCGGGTTCGAGCAGTTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGA T C MSL2 Ensembl:ENSG00000174579 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1351528473 Functional Loss SNV dbSNP153 33..33 33 - - - 47500 RMVar_ID_47500 Human_SNP_ID_154651502 A-to-I Human chr3 - 136184344 136184344 136184344 TGCCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGACATGAGCTACTGTGCCCAGCCCAGAACC TGCCTGCCTTGGCCTCCCAAAGTGCTGGGATTGCAGACATGAGCTACTGTGCCCAGCCCAGAACC T C MSL2 Ensembl:ENSG00000174579 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs574735150 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14633811 47501 RMVar_ID_47501 Human_SNP_ID_154653999 A-to-I Human chr3 - 136191711 136191711 136191711 TGGAGTGCAGTGGTGCGATCCTAGCTCACTGCAGCCTTAAACTCCTGGATTCATGCAGTCCTTCC TGGAGTGCAGTGGTGCGATCCTAGCTCACTGCTGCCTTAAACTCCTGGATTCATGCAGTCCTTCC T A MSL2 Ensembl:ENSG00000174579 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1317386880 Functional Loss SNV dbSNP153 33..33 33 - - - 47502 RMVar_ID_47502 Human_SNP_ID_154654212 A-to-I Human chr3 - 136192303 136192303 136192303 GTGGTGGCAGGTGCCTGTAATCCCAGTTACTCAGGAGGCTGAGGCCGATCTCCAGACATTGCTTG GTGGTGGCAGGTGCCTGTAATCCCAGTTACTCGGGAGGCTGAGGCCGATCTCCAGACATTGCTTG T C MSL2 Ensembl:ENSG00000174579 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs908327997 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14634149,Human_RBP_ID_20825086 47503 RMVar_ID_47503 Human_SNP_ID_154693059 A-to-I Human chr3 + 136331402 136331402 136331402 TAGGTCAGGAGTTTGAGACCATCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAA TAGGTCAGGAGTTTGAGACCATCCTGGCCAACGTGGTGAAACCCCATCTCTACTAAAAATACAAA A G PCCB Ensembl:ENSG00000114054 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1261882961 Functional Loss SNV dbSNP153 33..33 33 - - - 47504 RMVar_ID_47504 Human_SNP_ID_154693076 A-to-I Human chr3 + 136331471 136331471 136331471 AGCCGGATGTGGAGGCACATGCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACCTG AGCCGGATGTGGAGGCACATGCCCAGCTACTCCGGAGGCTGAGGCAGGAGAATCGCTTGAACCTG A C PCCB Ensembl:ENSG00000114054 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs998627097 Functional Loss SNV dbSNP153 33..33 33 - - - 47505 RMVar_ID_47505 Human_SNP_ID_154693097 A-to-I Human chr3 + 136331560 136331560 136331560 AGATCACACCACTGTGCTCCAGCCTGGGTGACAAAGCTAGATTCTGTCTCAGAAAATTAAATAAA AGATCACACCACTGTGCTCCAGCCTGGGTGACGAAGCTAGATTCTGTCTCAGAAAATTAAATAAA A G PCCB Ensembl:ENSG00000114054 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1244800536 Functional Loss SNV dbSNP153 33..33 33 - - - 47506 RMVar_ID_47506 Human_SNP_ID_154693098 A-to-I Human chr3 + 136331561 136331561 136331561 GATCACACCACTGTGCTCCAGCCTGGGTGACAAAGCTAGATTCTGTCTCAGAAAATTAAATAAAT GATCACACCACTGTGCTCCAGCCTGGGTGACAGAGCTAGATTCTGTCTCAGAAAATTAAATAAAT A G PCCB Ensembl:ENSG00000114054 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs112768868 Functional Loss SNV dbSNP153 33..33 33 - - - 47507 RMVar_ID_47507 Human_SNP_ID_154693099 A-to-I Human chr3 + 136331561 136331561 136331561 GATCACACCACTGTGCTCCAGCCTGGGTGACAAAGCTAGATTCTGTCTCAGAAAATTAAATAAAT GATCACACCACTGTGCTCCAGCCTGGGTGACATAGCTAGATTCTGTCTCAGAAAATTAAATAAAT A T PCCB Ensembl:ENSG00000114054 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs112768868 Functional Loss SNV dbSNP153 33..33 33 - - - 47508 RMVar_ID_47508 Human_SNP_ID_154693180 A-to-I Human chr3 + 136331844 136331844 136331844 CGCTCTGTCGCCAGGCTGGAGTGCGGTGGCGCAATCTCGACTCACTGCAACCTCTGCCTCCCAGG CGCTCTGTCGCCAGGCTGGAGTGCGGTGGCGCGATCTCGACTCACTGCAACCTCTGCCTCCCAGG A G PCCB Ensembl:ENSG00000114054 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1400068231 Functional Loss SNV dbSNP153 33..33 33 - - - 47509 RMVar_ID_47509 Human_SNP_ID_154713122 A-to-I Human chr3 - 136405517 136405517 136405517 GATGTTGAGGCTGGACGCGGTGTCCTATGTCTATAATCCCAGCACTTTGAGAGGTCGATACAGGC GATGTTGAGGCTGGACGCGGTGTCCTATGTCTGTAATCCCAGCACTTTGAGAGGTCGATACAGGC T C STAG1 Ensembl:ENSG00000118007 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs375394613 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26191,RMVar_hsa_circ_99674,RMVar_hsa_circ_221562,RMVar_hsa_circ_34580,RMVar_hsa_circ_56127,RMVar_hsa_circ_107612,RMVar_hsa_circ_221565,RMVar_hsa_circ_373679,RMVar_hsa_circ_44526,RMVar_hsa_circ_64968,RMVar_hsa_circ_346041,RMVar_hsa_circ_221566,RMVar_hsa_circ_364651,RMVar_hsa_circ_57401,RMVar_hsa_circ_61689,RMVar_hsa_circ_221573,RMVar_hsa_circ_265089,RMVar_hsa_circ_268740,RMVar_hsa_circ_347271,RMVar_hsa_circ_309922,RMVar_hsa_circ_9253,RMVar_hsa_circ_58670,RMVar_hsa_circ_266590,RMVar_hsa_circ_297531,RMVar_hsa_circ_60956,RMVar_hsa_circ_31195,RMVar_hsa_circ_316408,RMVar_hsa_circ_221575,RMVar_hsa_circ_18721,RMVar_hsa_circ_344067,RMVar_hsa_circ_359218,RMVar_hsa_circ_280137,RMVar_hsa_circ_70343,RMVar_hsa_circ_306054,RMVar_hsa_circ_221581,RMVar_hsa_circ_221579,RMVar_hsa_circ_221580,RMVar_hsa_circ_323956,RMVar_hsa_circ_348465,RMVar_hsa_circ_352868,RMVar_hsa_circ_363905,RMVar_hsa_circ_350021,RMVar_hsa_circ_324928,RMVar_hsa_circ_310651,RMVar_hsa_circ_63029,RMVar_hsa_circ_291889,RMVar_hsa_circ_294705,RMVar_hsa_circ_276023,RMVar_hsa_circ_52321,RMVar_hsa_circ_55139,RMVar_hsa_circ_34770,RMVar_hsa_circ_221583,RMVar_hsa_circ_221585,RMVar_hsa_circ_221587,RMVar_hsa_circ_221588,RMVar_hsa_circ_221586,RMVar_hsa_circ_221584,RMVar_hsa_circ_221582 47510 RMVar_ID_47510 Human_SNP_ID_154713678 A-to-I Human chr3 - 136407570 136407570 136407570 GTAATCCCAGCTACTTGAGAGGCTGAGGCATGAGAATGACTTGAACCTGGGAGGCAGAGGTTGCA GTAATCCCAGCTACTTGAGAGGCTGAGGCATGGGAATGACTTGAACCTGGGAGGCAGAGGTTGCA T C STAG1 Ensembl:ENSG00000118007 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1237294652 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26191,RMVar_hsa_circ_99674,RMVar_hsa_circ_221562,RMVar_hsa_circ_34580,RMVar_hsa_circ_56127,RMVar_hsa_circ_107612,RMVar_hsa_circ_221565,RMVar_hsa_circ_373679,RMVar_hsa_circ_44526,RMVar_hsa_circ_64968,RMVar_hsa_circ_346041,RMVar_hsa_circ_221566,RMVar_hsa_circ_364651,RMVar_hsa_circ_57401,RMVar_hsa_circ_61689,RMVar_hsa_circ_221573,RMVar_hsa_circ_265089,RMVar_hsa_circ_268740,RMVar_hsa_circ_347271,RMVar_hsa_circ_309922,RMVar_hsa_circ_9253,RMVar_hsa_circ_58670,RMVar_hsa_circ_266590,RMVar_hsa_circ_297531,RMVar_hsa_circ_60956,RMVar_hsa_circ_31195,RMVar_hsa_circ_316408,RMVar_hsa_circ_221575,RMVar_hsa_circ_18721,RMVar_hsa_circ_344067,RMVar_hsa_circ_359218,RMVar_hsa_circ_280137,RMVar_hsa_circ_70343,RMVar_hsa_circ_306054,RMVar_hsa_circ_221581,RMVar_hsa_circ_221579,RMVar_hsa_circ_221580,RMVar_hsa_circ_323956,RMVar_hsa_circ_348465,RMVar_hsa_circ_352868,RMVar_hsa_circ_363905,RMVar_hsa_circ_350021,RMVar_hsa_circ_324928,RMVar_hsa_circ_310651,RMVar_hsa_circ_63029,RMVar_hsa_circ_291889,RMVar_hsa_circ_294705,RMVar_hsa_circ_276023,RMVar_hsa_circ_52321,RMVar_hsa_circ_55139,RMVar_hsa_circ_34770,RMVar_hsa_circ_221583,RMVar_hsa_circ_221585,RMVar_hsa_circ_221587,RMVar_hsa_circ_221588,RMVar_hsa_circ_221586,RMVar_hsa_circ_221584,RMVar_hsa_circ_221582 47511 RMVar_ID_47511 Human_SNP_ID_154724290 A-to-I Human chr3 - 136447000 136447000 136447000 CAGGAGTTCGAGACCAGCCTGGCCAACATAGTAAAACACAGTCTCAACTAAAAATACAAAAATTA CAGGAGTTCGAGACCAGCCTGGCCAACATAGTGAAACACAGTCTCAACTAAAAATACAAAAATTA T C STAG1 Ensembl:ENSG00000118007 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1387241700 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_457,RMVar_hsa_circ_26191,RMVar_hsa_circ_99674,RMVar_hsa_circ_221562,RMVar_hsa_circ_56127,RMVar_hsa_circ_373679,RMVar_hsa_circ_44526,RMVar_hsa_circ_221566,RMVar_hsa_circ_364651,RMVar_hsa_circ_57401,RMVar_hsa_circ_265089,RMVar_hsa_circ_309922,RMVar_hsa_circ_9253,RMVar_hsa_circ_58670,RMVar_hsa_circ_60956,RMVar_hsa_circ_31195,RMVar_hsa_circ_316408,RMVar_hsa_circ_306054,RMVar_hsa_circ_348465,RMVar_hsa_circ_352868,RMVar_hsa_circ_363905,RMVar_hsa_circ_350021,RMVar_hsa_circ_294705,RMVar_hsa_circ_52321,RMVar_hsa_circ_55139,RMVar_hsa_circ_74540,RMVar_hsa_circ_221583,RMVar_hsa_circ_221584,RMVar_hsa_circ_311397,RMVar_hsa_circ_319547,RMVar_hsa_circ_368233,RMVar_hsa_circ_221582,RMVar_hsa_circ_279592,RMVar_hsa_circ_47066,RMVar_hsa_circ_221592,RMVar_hsa_circ_6847,RMVar_hsa_circ_366931,RMVar_hsa_circ_55486,RMVar_hsa_circ_364177,RMVar_hsa_circ_268194,RMVar_hsa_circ_37970,RMVar_hsa_circ_346727,RMVar_hsa_circ_349642,RMVar_hsa_circ_289818,RMVar_hsa_circ_15347,RMVar_hsa_circ_17249,RMVar_hsa_circ_294788,RMVar_hsa_circ_221595,RMVar_hsa_circ_221596,RMVar_hsa_circ_349971,RMVar_hsa_circ_350270,RMVar_hsa_circ_321157,RMVar_hsa_circ_68452,RMVar_hsa_circ_274135,RMVar_hsa_circ_61270,RMVar_hsa_circ_221597,RMVar_hsa_circ_221598 47512 RMVar_ID_47512 Human_SNP_ID_154724292 A-to-I Human chr3 - 136447003 136447003 136447003 GGTCAGGAGTTCGAGACCAGCCTGGCCAACATAGTAAAACACAGTCTCAACTAAAAATACAAAAA GGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTAAAACACAGTCTCAACTAAAAATACAAAAA T C STAG1 Ensembl:ENSG00000118007 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1399171124 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_457,RMVar_hsa_circ_26191,RMVar_hsa_circ_99674,RMVar_hsa_circ_221562,RMVar_hsa_circ_56127,RMVar_hsa_circ_373679,RMVar_hsa_circ_44526,RMVar_hsa_circ_221566,RMVar_hsa_circ_364651,RMVar_hsa_circ_57401,RMVar_hsa_circ_265089,RMVar_hsa_circ_309922,RMVar_hsa_circ_9253,RMVar_hsa_circ_58670,RMVar_hsa_circ_60956,RMVar_hsa_circ_31195,RMVar_hsa_circ_316408,RMVar_hsa_circ_306054,RMVar_hsa_circ_348465,RMVar_hsa_circ_352868,RMVar_hsa_circ_363905,RMVar_hsa_circ_350021,RMVar_hsa_circ_294705,RMVar_hsa_circ_52321,RMVar_hsa_circ_55139,RMVar_hsa_circ_74540,RMVar_hsa_circ_221583,RMVar_hsa_circ_221584,RMVar_hsa_circ_311397,RMVar_hsa_circ_319547,RMVar_hsa_circ_368233,RMVar_hsa_circ_221582,RMVar_hsa_circ_279592,RMVar_hsa_circ_47066,RMVar_hsa_circ_221592,RMVar_hsa_circ_6847,RMVar_hsa_circ_366931,RMVar_hsa_circ_55486,RMVar_hsa_circ_364177,RMVar_hsa_circ_268194,RMVar_hsa_circ_37970,RMVar_hsa_circ_346727,RMVar_hsa_circ_349642,RMVar_hsa_circ_289818,RMVar_hsa_circ_15347,RMVar_hsa_circ_17249,RMVar_hsa_circ_294788,RMVar_hsa_circ_221595,RMVar_hsa_circ_221596,RMVar_hsa_circ_349971,RMVar_hsa_circ_350270,RMVar_hsa_circ_321157,RMVar_hsa_circ_68452,RMVar_hsa_circ_274135,RMVar_hsa_circ_61270,RMVar_hsa_circ_221597,RMVar_hsa_circ_221598 47513 RMVar_ID_47513 Human_SNP_ID_154739150 A-to-I Human chr3 - 136494156 136494156 136494156 AGCAGTCCTCCTGCCTCAGCTCCCAAGTAGCTAGGACTGCAGGCAAGCTTCACGACACCTGGCCA AGCAGTCCTCCTGCCTCAGCTCCCAAGTAGCTGGGACTGCAGGCAAGCTTCACGACACCTGGCCA T C STAG1 Ensembl:ENSG00000118007 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1413240449 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14635306 RMVar_hsa_circ_457,RMVar_hsa_circ_56127,RMVar_hsa_circ_373679,RMVar_hsa_circ_44526,RMVar_hsa_circ_221566,RMVar_hsa_circ_364651,RMVar_hsa_circ_309922,RMVar_hsa_circ_31195,RMVar_hsa_circ_316408,RMVar_hsa_circ_352868,RMVar_hsa_circ_363905,RMVar_hsa_circ_294705,RMVar_hsa_circ_52321,RMVar_hsa_circ_55139,RMVar_hsa_circ_74540,RMVar_hsa_circ_221583,RMVar_hsa_circ_221582,RMVar_hsa_circ_279592,RMVar_hsa_circ_47066,RMVar_hsa_circ_221592,RMVar_hsa_circ_6847,RMVar_hsa_circ_364177,RMVar_hsa_circ_346727,RMVar_hsa_circ_15347,RMVar_hsa_circ_40674,RMVar_hsa_circ_294788,RMVar_hsa_circ_221596,RMVar_hsa_circ_349971,RMVar_hsa_circ_61270,RMVar_hsa_circ_68680,RMVar_hsa_circ_221598,RMVar_hsa_circ_307030,RMVar_hsa_circ_221601,RMVar_hsa_circ_271558,RMVar_hsa_circ_221600,RMVar_hsa_circ_338771,RMVar_hsa_circ_357877,RMVar_hsa_circ_371491,RMVar_hsa_circ_50645,RMVar_hsa_circ_90420,RMVar_hsa_circ_221603,RMVar_hsa_circ_221602,RMVar_hsa_circ_221607,RMVar_hsa_circ_316964,RMVar_hsa_circ_329401,RMVar_hsa_circ_354151,RMVar_hsa_circ_221606,RMVar_hsa_circ_14145,RMVar_hsa_circ_62827,RMVar_hsa_circ_358167 47514 RMVar_ID_47514 Human_SNP_ID_154739160 A-to-I Human chr3 - 136494188 136494188 136494188 CAACTCCGTAGAACCTCAATGTCCTGGGCTCAAGCAGTCCTCCTGCCTCAGCTCCCAAGTAGCTA CAACTCCGTAGAACCTCAATGTCCTGGGCTCAGGCAGTCCTCCTGCCTCAGCTCCCAAGTAGCTA T C STAG1 Ensembl:ENSG00000118007 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1310326746 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14635307 RMVar_hsa_circ_457,RMVar_hsa_circ_56127,RMVar_hsa_circ_373679,RMVar_hsa_circ_44526,RMVar_hsa_circ_221566,RMVar_hsa_circ_364651,RMVar_hsa_circ_309922,RMVar_hsa_circ_31195,RMVar_hsa_circ_316408,RMVar_hsa_circ_352868,RMVar_hsa_circ_363905,RMVar_hsa_circ_294705,RMVar_hsa_circ_52321,RMVar_hsa_circ_55139,RMVar_hsa_circ_74540,RMVar_hsa_circ_221583,RMVar_hsa_circ_221582,RMVar_hsa_circ_279592,RMVar_hsa_circ_47066,RMVar_hsa_circ_221592,RMVar_hsa_circ_6847,RMVar_hsa_circ_364177,RMVar_hsa_circ_346727,RMVar_hsa_circ_15347,RMVar_hsa_circ_40674,RMVar_hsa_circ_294788,RMVar_hsa_circ_221596,RMVar_hsa_circ_349971,RMVar_hsa_circ_61270,RMVar_hsa_circ_68680,RMVar_hsa_circ_221598,RMVar_hsa_circ_307030,RMVar_hsa_circ_221601,RMVar_hsa_circ_271558,RMVar_hsa_circ_221600,RMVar_hsa_circ_338771,RMVar_hsa_circ_357877,RMVar_hsa_circ_371491,RMVar_hsa_circ_50645,RMVar_hsa_circ_90420,RMVar_hsa_circ_221603,RMVar_hsa_circ_221602,RMVar_hsa_circ_221607,RMVar_hsa_circ_316964,RMVar_hsa_circ_329401,RMVar_hsa_circ_354151,RMVar_hsa_circ_221606,RMVar_hsa_circ_14145,RMVar_hsa_circ_62827,RMVar_hsa_circ_358167 47515 RMVar_ID_47515 Human_SNP_ID_154743260 A-to-I Human chr3 - 136508522 136508522 136508522 CTCAATGCCCAGGTAATTTTTAAATTTTTTGTAGAGATGGAGTCTTGCTATGTTACCCAGGCTGG CTCAATGCCCAGGTAATTTTTAAATTTTTTGTGGAGATGGAGTCTTGCTATGTTACCCAGGCTGG T C STAG1 Ensembl:ENSG00000118007 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs375007099 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_457,RMVar_hsa_circ_56127,RMVar_hsa_circ_44526,RMVar_hsa_circ_31195,RMVar_hsa_circ_352868,RMVar_hsa_circ_363905,RMVar_hsa_circ_52321,RMVar_hsa_circ_55139,RMVar_hsa_circ_74540,RMVar_hsa_circ_221582,RMVar_hsa_circ_47066,RMVar_hsa_circ_6847,RMVar_hsa_circ_15347,RMVar_hsa_circ_28146,RMVar_hsa_circ_40674,RMVar_hsa_circ_221596,RMVar_hsa_circ_349971,RMVar_hsa_circ_61270,RMVar_hsa_circ_68680,RMVar_hsa_circ_221601,RMVar_hsa_circ_338771,RMVar_hsa_circ_357877,RMVar_hsa_circ_371491,RMVar_hsa_circ_50645,RMVar_hsa_circ_90420,RMVar_hsa_circ_221602,RMVar_hsa_circ_221607,RMVar_hsa_circ_329401,RMVar_hsa_circ_354151,RMVar_hsa_circ_31111,RMVar_hsa_circ_296022,RMVar_hsa_circ_347148,RMVar_hsa_circ_62827,RMVar_hsa_circ_351835,RMVar_hsa_circ_290130,RMVar_hsa_circ_221609,RMVar_hsa_circ_27716,RMVar_hsa_circ_221608 47516 RMVar_ID_47516 Human_SNP_ID_154743261 A-to-I Human chr3 - 136508522 136508522 136508522 CTCAATGCCCAGGTAATTTTTAAATTTTTTGTAGAGATGGAGTCTTGCTATGTTACCCAGGCTGG CTCAATGCCCAGGTAATTTTTAAATTTTTTGTCGAGATGGAGTCTTGCTATGTTACCCAGGCTGG T G STAG1 Ensembl:ENSG00000118007 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs375007099 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_457,RMVar_hsa_circ_56127,RMVar_hsa_circ_44526,RMVar_hsa_circ_31195,RMVar_hsa_circ_352868,RMVar_hsa_circ_363905,RMVar_hsa_circ_52321,RMVar_hsa_circ_55139,RMVar_hsa_circ_74540,RMVar_hsa_circ_221582,RMVar_hsa_circ_47066,RMVar_hsa_circ_6847,RMVar_hsa_circ_15347,RMVar_hsa_circ_28146,RMVar_hsa_circ_40674,RMVar_hsa_circ_221596,RMVar_hsa_circ_349971,RMVar_hsa_circ_61270,RMVar_hsa_circ_68680,RMVar_hsa_circ_221601,RMVar_hsa_circ_338771,RMVar_hsa_circ_357877,RMVar_hsa_circ_371491,RMVar_hsa_circ_50645,RMVar_hsa_circ_90420,RMVar_hsa_circ_221602,RMVar_hsa_circ_221607,RMVar_hsa_circ_329401,RMVar_hsa_circ_354151,RMVar_hsa_circ_31111,RMVar_hsa_circ_296022,RMVar_hsa_circ_347148,RMVar_hsa_circ_62827,RMVar_hsa_circ_351835,RMVar_hsa_circ_290130,RMVar_hsa_circ_221609,RMVar_hsa_circ_27716,RMVar_hsa_circ_221608 47517 RMVar_ID_47517 Human_SNP_ID_154743790 A-to-I Human chr3 - 136510392 136510392 136510392 TCAGCCACTAGGGAGGCTGAGGCACGAGAATCACTTGAACCAGGGAGGCGGGGGTTGCAGTGAGC TCAGCCACTAGGGAGGCTGAGGCACGAGAATCGCTTGAACCAGGGAGGCGGGGGTTGCAGTGAGC T C STAG1 Ensembl:ENSG00000118007 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1157570634 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_457,RMVar_hsa_circ_56127,RMVar_hsa_circ_44526,RMVar_hsa_circ_31195,RMVar_hsa_circ_352868,RMVar_hsa_circ_363905,RMVar_hsa_circ_52321,RMVar_hsa_circ_55139,RMVar_hsa_circ_74540,RMVar_hsa_circ_221582,RMVar_hsa_circ_47066,RMVar_hsa_circ_6847,RMVar_hsa_circ_15347,RMVar_hsa_circ_28146,RMVar_hsa_circ_40674,RMVar_hsa_circ_221596,RMVar_hsa_circ_349971,RMVar_hsa_circ_61270,RMVar_hsa_circ_68680,RMVar_hsa_circ_221601,RMVar_hsa_circ_338771,RMVar_hsa_circ_357877,RMVar_hsa_circ_371491,RMVar_hsa_circ_50645,RMVar_hsa_circ_90420,RMVar_hsa_circ_221602,RMVar_hsa_circ_221607,RMVar_hsa_circ_329401,RMVar_hsa_circ_354151,RMVar_hsa_circ_31111,RMVar_hsa_circ_296022,RMVar_hsa_circ_347148,RMVar_hsa_circ_62827,RMVar_hsa_circ_351835,RMVar_hsa_circ_290130,RMVar_hsa_circ_221609,RMVar_hsa_circ_27716,RMVar_hsa_circ_221608 47518 RMVar_ID_47518 Human_SNP_ID_154745131 A-to-I Human chr3 - 136515177 136515177 136515177 TATTTTTGGGAGAGACGGGGTTTTATCATGTTAGCCAGGCTAGTCTCGAACTCCTCACCTCGGGC TATTTTTGGGAGAGACGGGGTTTTATCATGTTTGCCAGGCTAGTCTCGAACTCCTCACCTCGGGC T A STAG1 Ensembl:ENSG00000118007 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1271578351 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8559644,Human_RBP_ID_14635669 RMVar_hsa_circ_457,RMVar_hsa_circ_56127,RMVar_hsa_circ_44526,RMVar_hsa_circ_31195,RMVar_hsa_circ_352868,RMVar_hsa_circ_363905,RMVar_hsa_circ_52321,RMVar_hsa_circ_55139,RMVar_hsa_circ_74540,RMVar_hsa_circ_221582,RMVar_hsa_circ_47066,RMVar_hsa_circ_6847,RMVar_hsa_circ_15347,RMVar_hsa_circ_28146,RMVar_hsa_circ_40674,RMVar_hsa_circ_221596,RMVar_hsa_circ_349971,RMVar_hsa_circ_61270,RMVar_hsa_circ_68680,RMVar_hsa_circ_221601,RMVar_hsa_circ_338771,RMVar_hsa_circ_357877,RMVar_hsa_circ_371491,RMVar_hsa_circ_50645,RMVar_hsa_circ_90420,RMVar_hsa_circ_221602,RMVar_hsa_circ_221607,RMVar_hsa_circ_329401,RMVar_hsa_circ_354151,RMVar_hsa_circ_31111,RMVar_hsa_circ_296022,RMVar_hsa_circ_347148,RMVar_hsa_circ_62827,RMVar_hsa_circ_351835,RMVar_hsa_circ_290130,RMVar_hsa_circ_221609,RMVar_hsa_circ_27716,RMVar_hsa_circ_221608 47519 RMVar_ID_47519 Human_SNP_ID_154766462 A-to-I Human chr3 - 136589186 136589186 136589186 CCTTGATTGGCTTTTTAAAGATAAAATAGGCCAGGTGCAGTGGCTCATGCCTGTAATCCCAACAC CCTTGATTGGCTTTTTAAAGATAAAATAGGCCGGGTGCAGTGGCTCATGCCTGTAATCCCAACAC T C STAG1 Ensembl:ENSG00000118007 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879543263 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44526,RMVar_hsa_circ_31195,RMVar_hsa_circ_352868,RMVar_hsa_circ_221582,RMVar_hsa_circ_6847,RMVar_hsa_circ_28146,RMVar_hsa_circ_61270,RMVar_hsa_circ_221601,RMVar_hsa_circ_371491,RMVar_hsa_circ_50645,RMVar_hsa_circ_90420,RMVar_hsa_circ_221602,RMVar_hsa_circ_354151,RMVar_hsa_circ_31111,RMVar_hsa_circ_351835,RMVar_hsa_circ_17180,RMVar_hsa_circ_302358,RMVar_hsa_circ_340368,RMVar_hsa_circ_360129,RMVar_hsa_circ_365937,RMVar_hsa_circ_22497,RMVar_hsa_circ_55688,RMVar_hsa_circ_26988,RMVar_hsa_circ_308090,RMVar_hsa_circ_221612,RMVar_hsa_circ_221610,RMVar_hsa_circ_221611,RMVar_hsa_circ_310156,RMVar_hsa_circ_351056,RMVar_hsa_circ_304786 47520 RMVar_ID_47520 Human_SNP_ID_154769263 A-to-I Human chr3 - 136599348 136599348 136599348 TTTTTTATTTTTAGTAGATACAGGGTTTTGCCATGTTACCCTAGGCTGGTCTTGAACTCCTGGAC TTTTTTATTTTTAGTAGATACAGGGTTTTGCCGTGTTACCCTAGGCTGGTCTTGAACTCCTGGAC T C STAG1 Ensembl:ENSG00000118007 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971509880 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44526,RMVar_hsa_circ_31195,RMVar_hsa_circ_352868,RMVar_hsa_circ_221582,RMVar_hsa_circ_6847,RMVar_hsa_circ_28146,RMVar_hsa_circ_61270,RMVar_hsa_circ_221601,RMVar_hsa_circ_371491,RMVar_hsa_circ_50645,RMVar_hsa_circ_90420,RMVar_hsa_circ_221602,RMVar_hsa_circ_354151,RMVar_hsa_circ_351835,RMVar_hsa_circ_302358,RMVar_hsa_circ_340368,RMVar_hsa_circ_360129,RMVar_hsa_circ_365937,RMVar_hsa_circ_22497,RMVar_hsa_circ_55688,RMVar_hsa_circ_26988,RMVar_hsa_circ_308090,RMVar_hsa_circ_221612,RMVar_hsa_circ_221610,RMVar_hsa_circ_221611,RMVar_hsa_circ_310156,RMVar_hsa_circ_351056 47521 RMVar_ID_47521 Human_SNP_ID_154770236 A-to-I Human chr3 - 136602834 136602834 136602834 TAATTTATTCATTATACTTTTGTTTCTGAGACAGAGTCTTGCTCCATTGCCCAGGTTGGAGTGCA TAATTTATTCATTATACTTTTGTTTCTGAGACTGAGTCTTGCTCCATTGCCCAGGTTGGAGTGCA T A STAG1 Ensembl:ENSG00000118007 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1166922517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2750354 RMVar_hsa_circ_44526,RMVar_hsa_circ_31195,RMVar_hsa_circ_352868,RMVar_hsa_circ_221582,RMVar_hsa_circ_6847,RMVar_hsa_circ_28146,RMVar_hsa_circ_61270,RMVar_hsa_circ_221601,RMVar_hsa_circ_371491,RMVar_hsa_circ_50645,RMVar_hsa_circ_90420,RMVar_hsa_circ_221602,RMVar_hsa_circ_354151,RMVar_hsa_circ_351835,RMVar_hsa_circ_302358,RMVar_hsa_circ_340368,RMVar_hsa_circ_360129,RMVar_hsa_circ_365937,RMVar_hsa_circ_22497,RMVar_hsa_circ_55688,RMVar_hsa_circ_26988,RMVar_hsa_circ_308090,RMVar_hsa_circ_221612,RMVar_hsa_circ_221610,RMVar_hsa_circ_221611,RMVar_hsa_circ_310156,RMVar_hsa_circ_351056 47522 RMVar_ID_47522 Human_SNP_ID_154780151 A-to-I Human chr3 - 136638706 136638706 136638706 CAGAGACGAGTTTTCACCATGTTGGCCAGGCTAGTCTTGAATTTCTGACCTCAGGTGATCTGTCC CAGAGACGAGTTTTCACCATGTTGGCCAGGCTGGTCTTGAATTTCTGACCTCAGGTGATCTGTCC T C STAG1 Ensembl:ENSG00000118007 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1302530045 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14636760 RMVar_hsa_circ_47258 47523 RMVar_ID_47523 Human_SNP_ID_154786394 A-to-I Human chr3 - 136662717 136662717 136662717 TCTAAGGCTGGGTGCGGTGGCTTTTGCCTGTAATCCTAGTACTTTGGGGGGCTGAGGCAGGGGAC TCTAAGGCTGGGTGCGGTGGCTTTTGCCTGTAGTCCTAGTACTTTGGGGGGCTGAGGCAGGGGAC T C STAG1 Ensembl:ENSG00000118007 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs531397614 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17574398,Human_RBP_ID_22480986 RMVar_hsa_circ_47258 47524 RMVar_ID_47524 Human_SNP_ID_154786431 A-to-I Human chr3 - 136662859 136662859 136662859 TTAGTAGAGATGCGATTTCACCATGTTGGCAAAGCTGGTCTTGAACTCCTCACCTCAGGTGATCC TTAGTAGAGATGCGATTTCACCATGTTGGCAAGGCTGGTCTTGAACTCCTCACCTCAGGTGATCC T C STAG1 Ensembl:ENSG00000118007 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs970116336 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47258 47525 RMVar_ID_47525 Human_SNP_ID_154787968 A-to-I Human chr3 - 136668146 136668146 136668146 TCATTGCAACCTCCATATTCTGGGTTCAAGCAATTCTTGTGCTTCAGCCTCTCGACATAGCTGGG TCATTGCAACCTCCATATTCTGGGTTCAAGCAGTTCTTGTGCTTCAGCCTCTCGACATAGCTGGG T C STAG1 Ensembl:ENSG00000118007 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1341466859 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47258 47526 RMVar_ID_47526 Human_SNP_ID_154793785 A-to-I Human chr3 - 136689964 136689964 136689964 GCTATCTTGGCTCACTGTAGCCTCTGCCTCCCAGGTTCAACTGATTCTCCTGTCTGCCTCCTGAG GCTATCTTGGCTCACTGTAGCCTCTGCCTCCCGGGTTCAACTGATTCTCCTGTCTGCCTCCTGAG T C STAG1 Ensembl:ENSG00000118007 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1464412611 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47258 47527 RMVar_ID_47527 Human_SNP_ID_154793947 A-to-I Human chr3 - 136690401 136690401 136690401 GAAACCTCATCTCTACTAAAAATACAAAAATTAGTTGGGCATGGTGGCGTGGGCCTGTAGTCCCA GAAACCTCATCTCTACTAAAAATACAAAAATTGGTTGGGCATGGTGGCGTGGGCCTGTAGTCCCA T C STAG1 Ensembl:ENSG00000118007 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs573267364 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47258 47528 RMVar_ID_47528 Human_SNP_ID_154794913 A-to-I Human chr3 - 136693769 136693766 136693769 AGCCTGGGAATTTGATACCAGCCTGGCAACATAATGAGACCCCGTCTCTTAAAAAAAAAAAAATA AGCCTGGGAATTTGATACCAGCCTGGCAACAT___GAGACCCCGTCTCTTAAAAAAAAAAAAATA CATT C STAG1 Ensembl:ENSG00000118007 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348014305 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_17573850 RMVar_hsa_circ_47258 47529 RMVar_ID_47529 Human_SNP_ID_154794913 A-to-I Human chr3 - 136693768 136693766 136693769 GCCTGGGAATTTGATACCAGCCTGGCAACATAATGAGACCCCGTCTCTTAAAAAAAAAAAAATAA GCCTGGGAATTTGATACCAGCCTGGCAACAT___GAGACCCCGTCTCTTAAAAAAAAAAAAATAA CATT C STAG1 Ensembl:ENSG00000118007 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348014305 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_17573850 RMVar_hsa_circ_47258 47530 RMVar_ID_47530 Human_SNP_ID_154795306 A-to-I Human chr3 - 136695361 136695361 136695361 GCAATCTCGGCGCACTGCAACCTCCACCTCCCAGTTTCAAGTGATTCTTCTGCCTCAACCTCCTG GCAATCTCGGCGCACTGCAACCTCCACCTCCCTGTTTCAAGTGATTCTTCTGCCTCAACCTCCTG T A STAG1 Ensembl:ENSG00000118007 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1281836313 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14637820 RMVar_hsa_circ_47258 47531 RMVar_ID_47531 Human_SNP_ID_154798398 A-to-I Human chr3 - 136706056 136706052 136706056 TGTTTGTTTGTTTATTTCTGAGACAGGGTCTCACTCTGTCTTCCAGACTGGAGTGCAGTGGCATG TGTTTGTTTGTTTATTTCTGAGACAGGGTCTC____TGTCTTCCAGACTGGAGTGCAGTGGCATG AGAGT A STAG1 Ensembl:ENSG00000118007 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs374785184 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_3687936,Human_RBP_ID_17151346 RMVar_hsa_circ_47258 47532 RMVar_ID_47532 Human_SNP_ID_154799952 A-to-I Human chr3 - 136712192 136712192 136712192 CTAATGTGATGAAATTCTGTCTCTACTAAAATACAAAAAATTAGCTGGGTGTGGTGGCGTGCGCC CTAATGTGATGAAATTCTGTCTCTACTAAAATCCAAAAAATTAGCTGGGTGTGGTGGCGTGCGCC T G STAG1 Ensembl:ENSG00000118007 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017613038 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47258 47533 RMVar_ID_47533 Human_SNP_ID_154799980 A-to-I Human chr3 - 136712295 136712295 136712295 AAGTTCTCTGTAGGCTGGGTGCGGTGGCTCACACCTGTAATCCCAGCACTTTTGGAGGCCGAGGC AAGTTCTCTGTAGGCTGGGTGCGGTGGCTCACGCCTGTAATCCCAGCACTTTTGGAGGCCGAGGC T C STAG1 Ensembl:ENSG00000118007 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs577547420 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47258 47534 RMVar_ID_47534 Human_SNP_ID_154801385 A-to-I Human chr3 - 136716376 136716376 136716376 TCACTGCAACCGCTGCCTGTAGGGTTCAAATAATTCTACTGTCTCAGCCTCCCGAGTAGCTGGCA TCACTGCAACCGCTGCCTGTAGGGTTCAAATAGTTCTACTGTCTCAGCCTCCCGAGTAGCTGGCA T C STAG1 Ensembl:ENSG00000118007 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1410710653 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14638483 RMVar_hsa_circ_47258 47535 RMVar_ID_47535 Human_SNP_ID_154802843 A-to-I Human chr3 - 136721633 136721633 136721633 CGCCCGCCTCAGCCTCCTGAAGTGCTGGGATTACAGGCGAGAGTCACCGCGCCCGGCCCCATAGT CGCCCGCCTCAGCCTCCTGAAGTGCTGGGATTGCAGGCGAGAGTCACCGCGCCCGGCCCCATAGT T C STAG1 Ensembl:ENSG00000118007 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs892038722 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47258 47536 RMVar_ID_47536 Human_SNP_ID_154806171 A-to-I Human chr3 - 136732813 136732813 136732813 ACGAGGTCAGGAGTTTGAGATCAGTGTGGCCAAGATGGTGAAACCCCGTCTTTACTGAAAATACA ACGAGGTCAGGAGTTTGAGATCAGTGTGGCCAGGATGGTGAAACCCCGTCTTTACTGAAAATACA T C STAG1 Ensembl:ENSG00000118007 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1179461684 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14639024 RMVar_hsa_circ_47258 47537 RMVar_ID_47537 Human_SNP_ID_154806866 A-to-I Human chr3 - 136735264 136735264 136735264 AAAATTAGCTGGGCATGATGTTGGCCACCTGTAGTCCTATCTACTCAGGAGGCTGAGGTGGGAGG AAAATTAGCTGGGCATGATGTTGGCCACCTGTGGTCCTATCTACTCAGGAGGCTGAGGTGGGAGG T C STAG1 Ensembl:ENSG00000118007 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1559980602 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8559798,Human_RBP_ID_14639082 RMVar_hsa_circ_47258 47538 RMVar_ID_47538 Human_SNP_ID_154806929 A-to-I Human chr3 - 136735529 136735529 136735529 TGGTGGCTGAGGCATGAGAATCACTTGAACCCAGGAGGCGGAGGTTCCAGTGAGCTGAGATCATG TGGTGGCTGAGGCATGAGAATCACTTGAACCCGGGAGGCGGAGGTTCCAGTGAGCTGAGATCATG T C STAG1 Ensembl:ENSG00000118007 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs532178266 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47258 47539 RMVar_ID_47539 Human_SNP_ID_154807288 A-to-I Human chr3 - 136736917 136736917 136736917 GAGGCTGTGGACAAAGCTTACAAGTTGCTACTAGATCAGGAGCAAAAGAAGAGGACCCTGGATGT GAGGCTGTGGACAAAGCTTACAAGTTGCTACTGGATCAGGAGCAAAAGAAGAGGACCCTGGATGT T C STAG1,AC117382.1 Ensembl:ENSG00000118007,Ensembl:ENSG00000240695 Protein coding,Pseudogene intron,exon GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs576394762 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8211012,Human_RBP_ID_10484685,Human_RBP_ID_14639108,Human_RBP_ID_19121198 RMVar_hsa_circ_47258 47540 RMVar_ID_47540 Human_SNP_ID_154807883 A-to-I Human chr3 - 136739337 136739337 136739337 TAAAATACGTTTTTTCGTAGAGACAGGGTCTCACCATGTTGCCAAGGTTGGTCTTGAACTCCTGG TAAAATACGTTTTTTCGTAGAGACAGGGTCTCGCCATGTTGCCAAGGTTGGTCTTGAACTCCTGG T C STAG1 Ensembl:ENSG00000118007 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs370443560 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14639185 RMVar_hsa_circ_47258 47541 RMVar_ID_47541 Human_SNP_ID_154808282 A-to-I Human chr3 - 136740618 136740618 136740618 AAAATTAGTTAGGTGTGGTAGTGCGCACCTGTAGTCCCAGCTACTTGGGGGGCTGAGGCAGAGGA AAAATTAGTTAGGTGTGGTAGTGCGCACCTGTGGTCCCAGCTACTTGGGGGGCTGAGGCAGAGGA T C STAG1 Ensembl:ENSG00000118007 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027569264 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25699146 RMVar_hsa_circ_47258 47542 RMVar_ID_47542 Human_SNP_ID_154809239 A-to-I Human chr3 - 136744288 136744288 136744288 AGTTTCGCCCTTGTTGCCCAGGCTGGAGTGCAATGGTGCAATCTCGGCTTACCGCATCCTCTGCT AGTTTCGCCCTTGTTGCCCAGGCTGGAGTGCAGTGGTGCAATCTCGGCTTACCGCATCCTCTGCT T C STAG1 Ensembl:ENSG00000118007 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs953467533 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47258 47543 RMVar_ID_47543 Human_SNP_ID_154810396 A-to-I Human chr3 - 136748245 136748245 136748245 AGGCATGTGCCAGTACACCTAGCTAATTTTTTATATATTTGGTAGAGACAGTGTTTCACCTTGTT AGGCATGTGCCAGTACACCTAGCTAATTTTTTGTATATTTGGTAGAGACAGTGTTTCACCTTGTT T C STAG1 Ensembl:ENSG00000118007 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947157388 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47258 47544 RMVar_ID_47544 Human_SNP_ID_154833833 A-to-I Human chr3 - 136841648 136841648 136841648 CGGCTCACCGCAACCTCCGCCTCCTGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCT CGGCTCACCGCAACCTCCGCCTCCTGGGTTCAGGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCT T C NCK1-DT Ensembl:ENSG00000239213 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1214794746 Functional Loss SNV dbSNP153 33..33 33 - - - 47545 RMVar_ID_47545 Human_SNP_ID_154841177 A-to-I Human chr3 + 136868602 136868602 136868602 AGCCTGCTTTGGCCTCCCAAAGTGCTGGGATTACAGGGATGAGCCACCGCACCTGGCCAGTGTTT AGCCTGCTTTGGCCTCCCAAAGTGCTGGGATTGCAGGGATGAGCCACCGCACCTGGCCAGTGTTT A G NCK1 Ensembl:ENSG00000158092 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs895445714 Functional Loss SNV dbSNP153 33..33 33 - - - 47546 RMVar_ID_47546 Human_SNP_ID_154841959 A-to-I Human chr3 + 136871253 136871252 136871253 GCCGGCCTTTACAAAAGTAAAAAAAAAAAATTAGCCAGGTTTGGCTGTGAGCGTCTGTAGTCCTA GCCGGCCTTTACAAAAGTAAAAAAAAAAAATT_GCCAGGTTTGGCTGTGAGCGTCTGTAGTCCTA TA T NCK1 Ensembl:ENSG00000158092 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1482616967 Functional Loss DEL dbSNP153 33..33 33 - - - 47547 RMVar_ID_47547 Human_SNP_ID_154844370 A-to-I Human chr3 + 136880648 136880648 136880648 CAATCAACAAACTTTGTTTGTTTGTTTTTTTGAGGCAGGTTCTTGCTCTGTGACCCATGCTAGAG CAATCAACAAACTTTGTTTGTTTGTTTTTTTGGGGCAGGTTCTTGCTCTGTGACCCATGCTAGAG A G NCK1 Ensembl:ENSG00000158092 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1429838559 Functional Loss SNV dbSNP153 33..33 33 - - - 47548 RMVar_ID_47548 Human_SNP_ID_155085568 A-to-I Human chr3 - 137881634 137881634 137881634 AAACAGTTGTTATCCTTGGTCATGGCACACTCACCTTCATAAACCTGAATAAGCACACCAGGCTG AAACAGTTGTTATCCTTGGTCATGGCACACTCGCCTTCATAAACCTGAATAAGCACACCAGGCTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878930471 Functional Loss SNV dbSNP153 33..33 33 - - - 47549 RMVar_ID_47549 Human_SNP_ID_155166080 A-to-I Human chr3 + 138214726 138214726 138214726 TCACCCAGGCTGGAGTGCAGCAGCGTGATCTCAACTCACTGCAACCTCTGCTTCCTGGGTTCAAG TCACCCAGGCTGGAGTGCAGCAGCGTGATCTCCACTCACTGCAACCTCTGCTTCCTGGGTTCAAG A C ARMC8 Ensembl:ENSG00000114098 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1201824892 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_221636,RMVar_hsa_circ_44817,RMVar_hsa_circ_48438,RMVar_hsa_circ_349181,RMVar_hsa_circ_221640,RMVar_hsa_circ_275358,RMVar_hsa_circ_221634,RMVar_hsa_circ_16620,RMVar_hsa_circ_309714,RMVar_hsa_circ_352161,RMVar_hsa_circ_369541,RMVar_hsa_circ_294701,RMVar_hsa_circ_55175,RMVar_hsa_circ_271176,RMVar_hsa_circ_221641,RMVar_hsa_circ_221638,RMVar_hsa_circ_221639,RMVar_hsa_circ_221637,RMVar_hsa_circ_221635 47550 RMVar_ID_47550 Human_SNP_ID_155168446 A-to-I Human chr3 + 138224580 138224580 138224580 GAGACCAGCCTGGCCAACACGGTGAAACTCCCATTTCTATTAAAACTACAGAAATTAACCGGGCA GAGACCAGCCTGGCCAACACGGTGAAACTCCCGTTTCTATTAAAACTACAGAAATTAACCGGGCA A G ARMC8 Ensembl:ENSG00000114098 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs771529799 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_221636,RMVar_hsa_circ_44817,RMVar_hsa_circ_221634,RMVar_hsa_circ_309714,RMVar_hsa_circ_352161,RMVar_hsa_circ_369541,RMVar_hsa_circ_294701,RMVar_hsa_circ_55175,RMVar_hsa_circ_271176,RMVar_hsa_circ_221638,RMVar_hsa_circ_221639,RMVar_hsa_circ_221637,RMVar_hsa_circ_22462,RMVar_hsa_circ_358894,RMVar_hsa_circ_221635,RMVar_hsa_circ_314567,RMVar_hsa_circ_283854,RMVar_hsa_circ_221643,RMVar_hsa_circ_221644,RMVar_hsa_circ_221645,RMVar_hsa_circ_336187 47551 RMVar_ID_47551 Human_SNP_ID_155176513 A-to-I Human chr3 + 138256617 138256611 138256617 TATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGTTCTCGATGTCCCGACCTCGTGA TATTTTTAGTAGAGACGGGGTTTCACC______GCCAGGATGTTCTCGATGTCCCGACCTCGTGA CGTGTTA C ARMC8 Ensembl:ENSG00000114098 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs368486610 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_14644060 RMVar_hsa_circ_352161,RMVar_hsa_circ_31727,RMVar_hsa_circ_221635,RMVar_hsa_circ_124653,RMVar_hsa_circ_268471,RMVar_hsa_circ_221647,RMVar_hsa_circ_300061,RMVar_hsa_circ_360161,RMVar_hsa_circ_37074,RMVar_hsa_circ_54849,RMVar_hsa_circ_22394,RMVar_hsa_circ_221649,RMVar_hsa_circ_321082,RMVar_hsa_circ_71855,RMVar_hsa_circ_325138,RMVar_hsa_circ_379030,RMVar_hsa_circ_279556,RMVar_hsa_circ_221650,RMVar_hsa_circ_221652,RMVar_hsa_circ_42038,RMVar_hsa_circ_266359,RMVar_hsa_circ_221653 47552 RMVar_ID_47552 Human_SNP_ID_155233285 A-to-I Human chr3 - 138498489 138498489 138498489 TCTACTAAAAATACAAAAAATTAGTCGGGCGTAGTGGCAGGCACTACAGGAGGCTACTCGAGAGG TCTACTAAAAATACAAAAAATTAGTCGGGCGTGGTGGCAGGCACTACAGGAGGCTACTCGAGAGG T C CEP70 Ensembl:ENSG00000114107 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs533988687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_157348 RMVar_hsa_circ_221666,RMVar_hsa_circ_68372,RMVar_hsa_circ_330536,RMVar_hsa_circ_368451,RMVar_hsa_circ_353498,RMVar_hsa_circ_282162,RMVar_hsa_circ_28749,RMVar_hsa_circ_61329,RMVar_hsa_circ_221667,RMVar_hsa_circ_221668 47553 RMVar_ID_47553 Human_SNP_ID_155233373 A-to-I Human chr3 - 138498864 138498864 138498864 TTTTTGTACTTTAGTAGACGTGGGGTTTCACCATGTTGGCCAGGCTAGTCTCGAACTCCTGACCT TTTTTGTACTTTAGTAGACGTGGGGTTTCACCGTGTTGGCCAGGCTAGTCTCGAACTCCTGACCT T C CEP70 Ensembl:ENSG00000114107 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256560282 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7127375 RMVar_hsa_circ_221666,RMVar_hsa_circ_68372,RMVar_hsa_circ_330536,RMVar_hsa_circ_368451,RMVar_hsa_circ_353498,RMVar_hsa_circ_282162,RMVar_hsa_circ_28749,RMVar_hsa_circ_61329,RMVar_hsa_circ_221667,RMVar_hsa_circ_221668 47554 RMVar_ID_47554 Human_SNP_ID_155233568 A-to-I Human chr3 - 138499771 138499768 138499772 GTGTGTGTGTGTGTGTGTGTAGAGAGAGAGATAGAGACAAGGTTGCACCATGTTGCCCAGACCAG GTGTGTGTGTGTGTGTGTGTAGAGAGAGAGA____GACAAGGTTGCACCATGTTGCCCAGACCAG CTCTA C CEP70 Ensembl:ENSG00000114107 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1301346686 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_23972691 RMVar_hsa_circ_221666,RMVar_hsa_circ_68372,RMVar_hsa_circ_330536,RMVar_hsa_circ_368451,RMVar_hsa_circ_353498,RMVar_hsa_circ_282162,RMVar_hsa_circ_28749,RMVar_hsa_circ_61329,RMVar_hsa_circ_221667,RMVar_hsa_circ_221668 47555 RMVar_ID_47555 Human_SNP_ID_155240852 A-to-I Human chr3 - 138528733 138528733 138528733 TCTCCTTGGCCTCCCCAAAGTGCTGGGATTACAGGTATGAGCCACCATCCTCAGCCTCTAATTTT TCTCCTTGGCCTCCCCAAAGTGCTGGGATTACTGGTATGAGCCACCATCCTCAGCCTCTAATTTT T A CEP70 Ensembl:ENSG00000114107 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1356995965 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_68372,RMVar_hsa_circ_330536,RMVar_hsa_circ_282162,RMVar_hsa_circ_28749,RMVar_hsa_circ_221667,RMVar_hsa_circ_221668,RMVar_hsa_circ_38778,RMVar_hsa_circ_318114,RMVar_hsa_circ_221679,RMVar_hsa_circ_68183,RMVar_hsa_circ_221671,RMVar_hsa_circ_303009,RMVar_hsa_circ_283168,RMVar_hsa_circ_221675,RMVar_hsa_circ_221676,RMVar_hsa_circ_221677,RMVar_hsa_circ_221674,RMVar_hsa_circ_221683,RMVar_hsa_circ_294373,RMVar_hsa_circ_10106,RMVar_hsa_circ_13379,RMVar_hsa_circ_360076,RMVar_hsa_circ_299779,RMVar_hsa_circ_317158,RMVar_hsa_circ_270865,RMVar_hsa_circ_278738,RMVar_hsa_circ_96880,RMVar_hsa_circ_221681,RMVar_hsa_circ_221682,RMVar_hsa_circ_221680,RMVar_hsa_circ_221678 47556 RMVar_ID_47556 Human_SNP_ID_155241913 A-to-I Human chr3 - 138533218 138533218 138533218 GTAGTGCAGTGGTGCGCTCTTGACTCACTGCAAGCTCCGCCTCCCGGGTTCAAGTGATTCTCCTG GTAGTGCAGTGGTGCGCTCTTGACTCACTGCATGCTCCGCCTCCCGGGTTCAAGTGATTCTCCTG T A CEP70 Ensembl:ENSG00000114107 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1302172395 Functional Loss SNV dbSNP153 33..33 33 - - - 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 47557 RMVar_ID_47557 Human_SNP_ID_155261414 A-to-I Human chr3 + 138614317 138614317 138614317 ACAAAATTAGCTGGGTGTTGTGGCACATGCCTATGGTCCCAGCTACTAAGGAGGCTGAGGTGGGA ACAAAATTAGCTGGGTGTTGTGGCACATGCCTGTGGTCCCAGCTACTAAGGAGGCTGAGGTGGGA A G FAIM Ensembl:ENSG00000158234 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs550169146 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103117,RMVar_hsa_circ_221695 47558 RMVar_ID_47558 Human_SNP_ID_155276697 A-to-I Human chr3 - 138679652 138679652 138679652 TTGAGCCCAGGAGGTCAAGGCTGCAGTGAGCCAAGATCACGCTACTGCACTTCAGCTTGTGTGAC TTGAGCCCAGGAGGTCAAGGCTGCAGTGAGCCGAGATCACGCTACTGCACTTCAGCTTGTGTGAC T C PIK3CB Ensembl:ENSG00000051382 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223174873 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19326,RMVar_hsa_circ_106041,RMVar_hsa_circ_51301,RMVar_hsa_circ_221700,RMVar_hsa_circ_343230,RMVar_hsa_circ_32648,RMVar_hsa_circ_221702,RMVar_hsa_circ_277613,RMVar_hsa_circ_321334,RMVar_hsa_circ_366634,RMVar_hsa_circ_368873,RMVar_hsa_circ_330632,RMVar_hsa_circ_60294,RMVar_hsa_circ_221705,RMVar_hsa_circ_81792,RMVar_hsa_circ_221703,RMVar_hsa_circ_221704,RMVar_hsa_circ_124157,RMVar_hsa_circ_221706 47559 RMVar_ID_47559 Human_SNP_ID_155291932 A-to-I Human chr3 - 138741781 138741781 138741781 CTCTGTTGCCCAGGCTGGAGTGCGATGGCGCAATCTTGGCTCCCTGCAACCTCAGCCCCCCAGTC CTCTGTTGCCCAGGCTGGAGTGCGATGGCGCAGTCTTGGCTCCCTGCAACCTCAGCCCCCCAGTC T C PIK3CB Ensembl:ENSG00000051382 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017797134 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4240,RMVar_hsa_circ_66653,RMVar_hsa_circ_62155,RMVar_hsa_circ_366795,RMVar_hsa_circ_13899,RMVar_hsa_circ_28380,RMVar_hsa_circ_21400,RMVar_hsa_circ_33078,RMVar_hsa_circ_221723,RMVar_hsa_circ_68754,RMVar_hsa_circ_318867,RMVar_hsa_circ_325764,RMVar_hsa_circ_283767,RMVar_hsa_circ_221735,RMVar_hsa_circ_221736,RMVar_hsa_circ_354154,RMVar_hsa_circ_55733,RMVar_hsa_circ_351870 47560 RMVar_ID_47560 Human_SNP_ID_155300330 A-to-I Human chr3 - 138776815 138776815 138776815 AGGCTCAAGTGATCCTCCTACCTCAGCCTCCCAAGTAGCTGGGACCACAAGTGCATGCCATCATG AGGCTCAAGTGATCCTCCTACCTCAGCCTCCCGAGTAGCTGGGACCACAAGTGCATGCCATCATG T C PIK3CB Ensembl:ENSG00000051382 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs899097907 Functional Loss SNV dbSNP153 33..33 33 - - - 47561 RMVar_ID_47561 Human_SNP_ID_155303300 A-to-I Human chr3 - 138788098 138788098 138788098 GCCAACATGGCAAAACCCCATCTCCACCAAAAATACAAAAACTAGCCAGGTGTGGTGGTGCATGC GCCAACATGGCAAAACCCCATCTCCACCAAAAGTACAAAAACTAGCCAGGTGTGGTGGTGCATGC T C PIK3CB Ensembl:ENSG00000051382 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1401745665 Functional Loss SNV dbSNP153 33..33 33 - - - 47562 RMVar_ID_47562 Human_SNP_ID_155311623 A-to-I Human chr3 - 138820658 138820658 138820658 GAAACCCTGTCTCTAATAAAAGTACAAAAATTAGCCAGGTGTGGTGGTGCGCACTTGTAATCTGA GAAACCCTGTCTCTAATAAAAGTACAAAAATTGGCCAGGTGTGGTGGTGCGCACTTGTAATCTGA T C PIK3CB Ensembl:ENSG00000051382 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1490178404 Functional Loss SNV dbSNP153 33..33 33 - - - 47563 RMVar_ID_47563 Human_SNP_ID_155311651 A-to-I Human chr3 - 138820789 138820789 138820789 GTAGCCATTTAACAGAATGAAGAAAGTGGACCAGGCACGGTGGCTCATGCCTATAATCCCAGCAT GTAGCCATTTAACAGAATGAAGAAAGTGGACCGGGCACGGTGGCTCATGCCTATAATCCCAGCAT T C PIK3CB Ensembl:ENSG00000051382 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444802880 Functional Loss SNV dbSNP153 33..33 33 - - - 47564 RMVar_ID_47564 Human_SNP_ID_155313248 A-to-I Human chr3 - 138826947 138826947 138826947 CTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGTGCCCACAACCACGCCCAGCTAATTTTG CTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTGCAGGTGCCCACAACCACGCCCAGCTAATTTTG T C PIK3CB Ensembl:ENSG00000051382 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1001729029 Functional Loss SNV dbSNP153 33..33 33 - - - 47565 RMVar_ID_47565 Human_SNP_ID_155443039 A-to-I Human chr3 + 139356927 139356927 139356927 AAATTTTCTTTTTAATTTAAACAGGTCTTTGCAAAAACAGAAGCACAGAAGGGAGCCTATATAGA AAATTTTCTTTTTAATTTAAACAGGTCTTTGCGAAAACAGAAGCACAGAAGGGAGCCTATATAGA A G MRPS22 Ensembl:ENSG00000175110 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs767763328 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_590612 Human_Splice_Rec_489684,Human_Splice_Rec_489706,Human_Splice_Rec_489722,Human_Splice_Rec_489736,Human_Splice_Rec_489748,Human_Splice_Rec_489782,Human_Splice_Rec_489798 Human_miRNA_ID_185123 RMVar_hsa_circ_112939,RMVar_hsa_circ_221745 47566 RMVar_ID_47566 Human_SNP_ID_155443044 A-to-I Human chr3 + 139356939 139356939 139356939 TAATTTAAACAGGTCTTTGCAAAAACAGAAGCACAGAAGGGAGCCTATATAGAACTAACACTGCA TAATTTAAACAGGTCTTTGCAAAAACAGAAGCCCAGAAGGGAGCCTATATAGAACTAACACTGCA A C MRPS22 Ensembl:ENSG00000175110 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355941150 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_590612,Human_RBP_ID_1618788,Human_RBP_ID_1950673,Human_RBP_ID_4724717,Human_RBP_ID_7128001,Human_RBP_ID_14646619 Human_Splice_Rec_489684,Human_Splice_Rec_489706,Human_Splice_Rec_489722,Human_Splice_Rec_489736,Human_Splice_Rec_489748,Human_Splice_Rec_489782,Human_Splice_Rec_489798 Human_miRNA_ID_185123 RMVar_hsa_circ_112939,RMVar_hsa_circ_221745 47567 RMVar_ID_47567 Human_SNP_ID_155443772 A-to-I Human chr3 - 139359145 139359144 139359146 GTAGTGAAACTCTGGAGAGAGAATCTCTCAAAAGTCAATCAGAAAGCAGCAGAATCCCTTGCTGA GTAGTGAAACTCTGGAGAGAGAATCTCTCAA__GTCAATCAGAAAGCAGCAGAATCCCTTGCTGA CTT C COPB2 Ensembl:ENSG00000184432 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1429466728 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_18013457,Human_RBP_ID_26824969,Human_RBP_ID_27046415 Human_Splice_Rec_489846,Human_Splice_Rec_489888 RMVar_hsa_circ_21046,RMVar_hsa_circ_96372,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_221757,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_369119,RMVar_hsa_circ_66047,RMVar_hsa_circ_221758,RMVar_hsa_circ_64109,RMVar_hsa_circ_335729,RMVar_hsa_circ_348730,RMVar_hsa_circ_28448,RMVar_hsa_circ_101913,RMVar_hsa_circ_221759 47568 RMVar_ID_47568 Human_SNP_ID_155443773 A-to-I Human chr3 - 139359145 139359145 139359145 GTAGTGAAACTCTGGAGAGAGAATCTCTCAAAAGTCAATCAGAAAGCAGCAGAATCCCTTGCTGA GTAGTGAAACTCTGGAGAGAGAATCTCTCAAAGGTCAATCAGAAAGCAGCAGAATCCCTTGCTGA T C COPB2 Ensembl:ENSG00000184432 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs768558522 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18013457,Human_RBP_ID_26824969,Human_RBP_ID_27046415 Human_Splice_Rec_489846,Human_Splice_Rec_489888 RMVar_hsa_circ_21046,RMVar_hsa_circ_96372,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_221757,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_369119,RMVar_hsa_circ_66047,RMVar_hsa_circ_221758,RMVar_hsa_circ_64109,RMVar_hsa_circ_335729,RMVar_hsa_circ_348730,RMVar_hsa_circ_28448,RMVar_hsa_circ_101913,RMVar_hsa_circ_221759 47569 RMVar_ID_47569 Human_SNP_ID_155450220 A-to-I Human chr3 - 139387111 139387111 139387111 CACCTCCCAGATTCAAGTGATTCTGCAGCCTCAGCCTGCCGAGTAGCTGGGACTGCAGGCGCGTG CACCTCCCAGATTCAAGTGATTCTGCAGCCTCGGCCTGCCGAGTAGCTGGGACTGCAGGCGCGTG T C COPB2 Ensembl:ENSG00000184432 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965002305 Functional Loss SNV dbSNP153 33..33 33 - - - 47570 RMVar_ID_47570 Human_SNP_ID_155451675 A-to-I Human chr3 + 139392384 139392384 139392384 CCCCTGCCTCAGTCTCCCCAGTAGCTGGGACTACGGGTGCACGCCACCACGCCTGGCTGATTTTT CCCCTGCCTCAGTCTCCCCAGTAGCTGGGACTGCGGGTGCACGCCACCACGCCTGGCTGATTTTT A G AC046134.2 Ensembl:ENSG00000248932 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1020963885 Functional Loss SNV dbSNP153 33..33 33 - - - 47571 RMVar_ID_47571 Human_SNP_ID_155475217 A-to-I Human chr3 + 139493812 139493812 139493812 CACCACTCTGCCACCCCCCTCCTCTGCCGGTCACAATGGAAGAAGAAATCACCATGCTTTTCATT CACCACTCTGCCACCCCCCTCCTCTGCCGGTCGCAATGGAAGAAGAAATCACCATGCTTTTCATT A G ACTG1P1,AC046134.2 Ensembl:ENSG00000178631,Ensembl:ENSG00000248932 Pseudogene,lincRNA exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs765360411 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1618827,Human_RBP_ID_22825185,Human_RBP_ID_27046448 47572 RMVar_ID_47572 Human_SNP_ID_155475486 A-to-I Human chr3 - 139494819 139494819 139494819 GATGGAGCCACCAATCCACACTGAGTACTTGCACTCTGGGGGCATGATGATCTTGATCTTCATGG GATGGAGCCACCAATCCACACTGAGTACTTGCGCTCTGGGGGCATGATGATCTTGATCTTCATGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs945178015 Functional Loss SNV dbSNP153 33..33 33 - - - 47573 RMVar_ID_47573 Human_SNP_ID_155475487 A-to-I Human chr3 - 139494819 139494819 139494819 GATGGAGCCACCAATCCACACTGAGTACTTGCACTCTGGGGGCATGATGATCTTGATCTTCATGG GATGGAGCCACCAATCCACACTGAGTACTTGCCCTCTGGGGGCATGATGATCTTGATCTTCATGG T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs945178015 Functional Loss SNV dbSNP153 33..33 33 - - - 47574 RMVar_ID_47574 Human_SNP_ID_155475494 A-to-I Human chr3 - 139494842 139494842 139494842 TGGAAGGTGGACAGTGAGGCCAGGATGGAGCCACCAATCCACACTGAGTACTTGCACTCTGGGGG TGGAAGGTGGACAGTGAGGCCAGGATGGAGCCGCCAATCCACACTGAGTACTTGCACTCTGGGGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1370761872 Functional Loss SNV dbSNP153 33..33 33 - - - 47575 RMVar_ID_47575 Human_SNP_ID_155736872 A-to-I Human chr3 - 140573049 140573049 140573049 CAGAAACCTGGCAGGTGGCCTTCCTGGGGATGAGTGACCTCATGGCAGCCTCTCCTGGGCAGTCT CAGAAACCTGGCAGGTGGCCTTCCTGGGGATGCGTGACCTCATGGCAGCCTCTCCTGGGCAGTCT T G - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1230430233 Functional Loss SNV dbSNP153 33..33 33 - - - 47576 RMVar_ID_47576 Human_SNP_ID_155934726 A-to-I Human chr3 + 141408337 141408337 141408337 GGGAGGCCAAGGCTGATGGATGACCTGAGGTCAGGAGTTCGGGACCAGCCTGGCCAACGTGGCAA GGGAGGCCAAGGCTGATGGATGACCTGAGGTCGGGAGTTCGGGACCAGCCTGGCCAACGTGGCAA A G ZBTB38 Ensembl:ENSG00000177311 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs987093453 Functional Loss SNV dbSNP153 33..33 33 - - - 47577 RMVar_ID_47577 Human_SNP_ID_155940179 A-to-I Human chr3 + 141433912 141433912 141433912 AAGTGATAATCTCCTAAAAGTGTGTTTTTATTAGTAAATCTTTAAGAGATTGCAGAGAGAACTGT AAGTGATAATCTCCTAAAAGTGTGTTTTTATTTGTAAATCTTTAAGAGATTGCAGAGAGAACTGT A T ZBTB38 Ensembl:ENSG00000177311 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1171062200 Functional Loss SNV dbSNP153 33..33 33 - - - 47578 RMVar_ID_47578 Human_SNP_ID_155943651 A-to-I Human chr3 - 141448221 141448221 141448221 ATATTTACTTTGGTCTAGAATTATCAGCATACAAGTCCACTTAAAAAATATCCACATATAAGGGC ATATTTACTTTGGTCTAGAATTATCAGCATACGAGTCCACTTAAAAAATATCCACATATAAGGGC T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs543768103 Functional Loss SNV dbSNP153 33..33 33 - - - 47579 RMVar_ID_47579 Human_SNP_ID_155977179 A-to-I Human chr3 + 141588921 141588920 141588921 TGGAGGGCAGTGGCATGATCTTGGCTCACTGCAACCTCTGCCTCCCGGATTCAAGCGATTGTCCT TGGAGGGCAGTGGCATGATCTTGGCTCACTGC_ACCTCTGCCTCCCGGATTCAAGCGATTGTCCT CA C RASA2 Ensembl:ENSG00000155903 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1412570607 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_82093,RMVar_hsa_circ_221819,RMVar_hsa_circ_365879,RMVar_hsa_circ_24733,RMVar_hsa_circ_221834,RMVar_hsa_circ_221828,RMVar_hsa_circ_306312,RMVar_hsa_circ_221837,RMVar_hsa_circ_40968,RMVar_hsa_circ_221842,RMVar_hsa_circ_367586,RMVar_hsa_circ_20366,RMVar_hsa_circ_289860,RMVar_hsa_circ_53015,RMVar_hsa_circ_221849,RMVar_hsa_circ_221850,RMVar_hsa_circ_318640,RMVar_hsa_circ_23117,RMVar_hsa_circ_221852,RMVar_hsa_circ_17590 47580 RMVar_ID_47580 Human_SNP_ID_155978752 A-to-I Human chr3 + 141595849 141595849 141595849 CAAGGTCTCACTTTGTTGCCCAGGGTGGTCTCAAACTCCTGGACCCAAGTGATCCTCCTGCCTCG CAAGGTCTCACTTTGTTGCCCAGGGTGGTCTCTAACTCCTGGACCCAAGTGATCCTCCTGCCTCG A T RASA2 Ensembl:ENSG00000155903 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1214699831 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25700956 RMVar_hsa_circ_82093,RMVar_hsa_circ_221819,RMVar_hsa_circ_365879,RMVar_hsa_circ_24733,RMVar_hsa_circ_221834,RMVar_hsa_circ_221828,RMVar_hsa_circ_306312,RMVar_hsa_circ_221837,RMVar_hsa_circ_40968,RMVar_hsa_circ_367586,RMVar_hsa_circ_20366,RMVar_hsa_circ_289860,RMVar_hsa_circ_53015,RMVar_hsa_circ_221849,RMVar_hsa_circ_221850,RMVar_hsa_circ_318640,RMVar_hsa_circ_23117,RMVar_hsa_circ_221852,RMVar_hsa_circ_17590 47581 RMVar_ID_47581 Human_SNP_ID_156015188 A-to-I Human chr3 + 141743107 141743107 141743107 GGTTCCTTGGGTATCCTAGTGTTTCTTGATGTATGTATAAACAAATGCTAACATATATATATGGT GGTTCCTTGGGTATCCTAGTGTTTCTTGATGTGTGTATAAACAAATGCTAACATATATATATGGT A G AC112504.2,RNF7 Ensembl:ENSG00000285558,Ensembl:ENSG00000114125 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025121386 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1619018 47582 RMVar_ID_47582 Human_SNP_ID_156016228 A-to-I Human chr3 + 141747691 141747691 141747691 CTCACGCTGTAATCCAAGCACTTTGGGAGGCCAAGGTGGGTGGATTGCCTGAGGTCAGGTGTTCG CTCACGCTGTAATCCAAGCACTTTGGGAGGCCGAGGTGGGTGGATTGCCTGAGGTCAGGTGTTCG A G AC112504.2 Ensembl:ENSG00000285558 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1200090212 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_221854 47583 RMVar_ID_47583 Human_SNP_ID_156016560 A-to-I Human chr3 + 141748954 141748954 141748954 AGATAATAATAACAATATAATAATTCTTGGCCAGGCGTGGTGGCTCATGCCTGTAATCCCAGCAC AGATAATAATAACAATATAATAATTCTTGGCCGGGCGTGGTGGCTCATGCCTGTAATCCCAGCAC A G AC112504.2 Ensembl:ENSG00000285558 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934195663 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_221854 47584 RMVar_ID_47584 Human_SNP_ID_156016591 A-to-I Human chr3 + 141749122 141749122 141749122 TGGAATGGTGGTGTGCACCTGTAATTCTAGCTACTCAGAAGGCTGAGGTGGGAGGATCGCTTAAG TGGAATGGTGGTGTGCACCTGTAATTCTAGCTCCTCAGAAGGCTGAGGTGGGAGGATCGCTTAAG A C AC112504.2 Ensembl:ENSG00000285558 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs544548476 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_221854 47585 RMVar_ID_47585 Human_SNP_ID_156047537 A-to-I Human chr3 - 141874919 141874919 141874919 GTAGCGGGCGCCTGTAGTCCCGGCTGCTCGGGAGGCTGAGGCAGGAGAATGGGGTGAACCCAGGA GTAGCGGGCGCCTGTAGTCCCGGCTGCTCGGGGGGCTGAGGCAGGAGAATGGGGTGAACCCAGGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1165002845 Functional Loss SNV dbSNP153 33..33 33 - - - 47586 RMVar_ID_47586 Human_SNP_ID_156049767 A-to-I Human chr3 + 141882683 141882683 141882683 TCGGCTCACCGCAACCTCTGCCTCCCGGATTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGC TCGGCTCACCGCAACCTCTGCCTCCCGGATTCGAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGC A G ATP1B3 Ensembl:ENSG00000069849 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973487167 Functional Loss SNV dbSNP153 33..33 33 - - - 47587 RMVar_ID_47587 Human_SNP_ID_156049903 A-to-I Human chr3 + 141883210 141883210 141883210 AACATCTTTGAACTCCTCTTTGCATTAAGGCCAGGTGCAGTGGCTCTTGCCTGTAATCCCAGCAC AACATCTTTGAACTCCTCTTTGCATTAAGGCCGGGTGCAGTGGCTCTTGCCTGTAATCCCAGCAC A G ATP1B3 Ensembl:ENSG00000069849 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1464013584 Functional Loss SNV dbSNP153 33..33 33 - - - 47588 RMVar_ID_47588 Human_SNP_ID_156050833 A-to-I Human chr3 + 141886918 141886918 141886918 CCAGCTACTCAGGAGGTTGAGGCTGGACAATCACTTGAGCCTGGGAGGTCAAGGCTGCAGTGAGC CCAGCTACTCAGGAGGTTGAGGCTGGACAATCTCTTGAGCCTGGGAGGTCAAGGCTGCAGTGAGC A T ATP1B3 Ensembl:ENSG00000069849 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1175736031 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14650498 47589 RMVar_ID_47589 Human_SNP_ID_156051974 A-to-I Human chr3 + 141890571 141890571 141890571 GTGATCTGCCCGCCTCAGCCTCCCACAGTGCTAGGATTACAGGCGTGAGCCACCACGCCCACCTA GTGATCTGCCCGCCTCAGCCTCCCACAGTGCTGGGATTACAGGCGTGAGCCACCACGCCCACCTA A G ATP1B3 Ensembl:ENSG00000069849 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1455169925 Functional Loss SNV dbSNP153 33..33 33 - - - 47590 RMVar_ID_47590 Human_SNP_ID_156051991 A-to-I Human chr3 + 141890618 141890618 141890618 AGCCACCACGCCCACCTAATTTTTGTATTTTTAGTAGAGACTGGGTTTTGCCATGTTGCCCAGGC AGCCACCACGCCCACCTAATTTTTGTATTTTTGGTAGAGACTGGGTTTTGCCATGTTGCCCAGGC A G ATP1B3 Ensembl:ENSG00000069849 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1304574574 Functional Loss SNV dbSNP153 33..33 33 - - - 47591 RMVar_ID_47591 Human_SNP_ID_156052023 A-to-I Human chr3 + 141890714 141890685 141890716 CCCACCTCTGCCTCCCACAGTGCTGGGATTACAGACGTGAGCCACCACGCCCACCTAATTTTTGT CCCGCCTCAGCCTCCCACAGTGCTAGGATTACAGGCGTGAGCCACCACGCCCACCTAATTTTTGT ACCTCTGCCTCCCACAGTGCTGGGATTACAGA GCCTCAGCCTCCCACAGTGCTAGGATTACAGG ATP1B3 Ensembl:ENSG00000069849 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs386666501 Functional Loss MNV dbSNP153 4..35 33 - - - 47592 RMVar_ID_47592 Human_SNP_ID_156052023 A-to-I Human chr3 + 141890712 141890685 141890716 TGCCCACCTCTGCCTCCCACAGTGCTGGGATTACAGACGTGAGCCACCACGCCCACCTAATTTTT TGCCCGCCTCAGCCTCCCACAGTGCTAGGATTACAGGCGTGAGCCACCACGCCCACCTAATTTTT ACCTCTGCCTCCCACAGTGCTGGGATTACAGA GCCTCAGCCTCCCACAGTGCTAGGATTACAGG ATP1B3 Ensembl:ENSG00000069849 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs386666501 Functional Loss MNV dbSNP153 6..37 33 - - - 47593 RMVar_ID_47593 Human_SNP_ID_156052070 A-to-I Human chr3 + 141890825 141890825 141890825 AAACTCCTGAGCTGAAGCGATCTGCCTGCCTCAGCCTCCCACAGTGCTGGGATCACAGGGGTGAG AAACTCCTGAGCTGAAGCGATCTGCCTGCCTCTGCCTCCCACAGTGCTGGGATCACAGGGGTGAG A T ATP1B3 Ensembl:ENSG00000069849 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1401758914 Functional Loss SNV dbSNP153 33..33 33 - - - 47594 RMVar_ID_47594 Human_SNP_ID_156053460 A-to-I Human chr3 + 141896406 141896406 141896406 AGCTGGGCACGGTGGTATGTGCCTGTAGTCCTAGCTACTGGGGAGGCTGGGGCAGGAGGATTGCT AGCTGGGCACGGTGGTATGTGCCTGTAGTCCTCGCTACTGGGGAGGCTGGGGCAGGAGGATTGCT A C ATP1B3 Ensembl:ENSG00000069849 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1171484439 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8560619,Human_RBP_ID_23973867 47595 RMVar_ID_47595 Human_SNP_ID_156054235 A-to-I Human chr3 + 141899927 141899927 141899927 GTGGCACACAACTGTAGTCCCAACTTCTCAGGAAGCTGAGACAGGAGAATCACTTGAGCCGAGGA GTGGCACACAACTGTAGTCCCAACTTCTCAGGGAGCTGAGACAGGAGAATCACTTGAGCCGAGGA A G ATP1B3 Ensembl:ENSG00000069849 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1559868845 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14650733 47596 RMVar_ID_47596 Human_SNP_ID_156055115 A-to-I Human chr3 + 141903618 141903618 141903618 GTGCACATTTCATAAGTTTTATTTTCTTTTACAGGTTTGATCTTGCTCTTCTACCTAGTTTTTTA GTGCACATTTCATAAGTTTTATTTTCTTTTACGGGTTTGATCTTGCTCTTCTACCTAGTTTTTTA A G ATP1B3 Ensembl:ENSG00000069849 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1245087319 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7129764,Human_RBP_ID_8560624,Human_RBP_ID_25701137 RMVar_hsa_circ_221855,RMVar_hsa_circ_22382,RMVar_hsa_circ_272709,RMVar_hsa_circ_310076,RMVar_hsa_circ_277329,RMVar_hsa_circ_49898,RMVar_hsa_circ_221856,RMVar_hsa_circ_278414,RMVar_hsa_circ_309092,RMVar_hsa_circ_346125,RMVar_hsa_circ_280068,RMVar_hsa_circ_904 47597 RMVar_ID_47597 Human_SNP_ID_156056755 A-to-I Human chr3 + 141910155 141910155 141910155 CATCACGCCTGGCTAATTTTTTAATTTTTTGTAGAGCTGGGGTCTTGCTATGTTGCCCAGGCTGG CATCACGCCTGGCTAATTTTTTAATTTTTTGTGGAGCTGGGGTCTTGCTATGTTGCCCAGGCTGG A G ATP1B3 Ensembl:ENSG00000069849 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs890376535 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14650951 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 47598 RMVar_ID_47598 Human_SNP_ID_156058421 A-to-I Human chr3 + 141916940 141916940 141916940 TGGGCTGGAGTGCAGTGGCACGATCTCACTGCAAGCTCCGCCTCCCGGGTTCACGCGGTTCTCCT TGGGCTGGAGTGCAGTGGCACGATCTCACTGCGAGCTCCGCCTCCCGGGTTCACGCGGTTCTCCT A G ATP1B3 Ensembl:ENSG00000069849 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1328329933 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14651121 RMVar_hsa_circ_49898,RMVar_hsa_circ_309092,RMVar_hsa_circ_317323 47599 RMVar_ID_47599 Human_SNP_ID_156058436 A-to-I Human chr3 + 141916978 141916978 141916978 CGCCTCCCGGGTTCACGCGGTTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCGCTCC CGCCTCCCGGGTTCACGCGGTTCTCCTGCCTCGGCCTCCTGAGTAGCTGGGACTACAGGCGCTCC A G ATP1B3 Ensembl:ENSG00000069849 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1163599003 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49898,RMVar_hsa_circ_309092,RMVar_hsa_circ_317323 47600 RMVar_ID_47600 Human_SNP_ID_156058569 A-to-I Human chr3 + 141917484 141917484 141917484 TTGGGAGGCTGAGGCAGGCAGATCACGAGGTCAAGAGATCGAGACCATCCTGGCCAACATACTGA TTGGGAGGCTGAGGCAGGCAGATCACGAGGTCCAGAGATCGAGACCATCCTGGCCAACATACTGA A C ATP1B3 Ensembl:ENSG00000069849 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1383546260 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49898,RMVar_hsa_circ_309092,RMVar_hsa_circ_317323 47601 RMVar_ID_47601 Human_SNP_ID_156058588 A-to-I Human chr3 + 141917555 141917555 141917555 GTCTCTACTAAAATACAGAAAATTAGCTGGGCATGGTGGCACGCACCTGTAGTCCCAGCTATTCA GTCTCTACTAAAATACAGAAAATTAGCTGGGCGTGGTGGCACGCACCTGTAGTCCCAGCTATTCA A G ATP1B3 Ensembl:ENSG00000069849 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1048524076 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14651138 RMVar_hsa_circ_49898,RMVar_hsa_circ_309092,RMVar_hsa_circ_317323 47602 RMVar_ID_47602 Human_SNP_ID_156058876 A-to-I Human chr3 + 141918578 141918578 141918578 CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCACGTGCTATCACGCCCGGTTAATTTTT CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTGCAGGCACGTGCTATCACGCCCGGTTAATTTTT A G ATP1B3 Ensembl:ENSG00000069849 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs758395363 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49898,RMVar_hsa_circ_309092,RMVar_hsa_circ_317323 47603 RMVar_ID_47603 Human_SNP_ID_156058916 A-to-I Human chr3 + 141918698 141918698 141918698 TGACCTCGTGATTCGTCTTCCTCAGCCTCCCAAAGTACTGGGGTAACAGGCGTGAGCCACTGCAC TGACCTCGTGATTCGTCTTCCTCAGCCTCCCAGAGTACTGGGGTAACAGGCGTGAGCCACTGCAC A G ATP1B3 Ensembl:ENSG00000069849 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1360897816 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49898,RMVar_hsa_circ_309092,RMVar_hsa_circ_317323 47604 RMVar_ID_47604 Human_SNP_ID_156059167 A-to-I Human chr3 + 141919710 141919710 141919710 CCTGTAATTCCAGCACTTTGGGAGGCCAAGGTAGGCGGATCACCAGAGGTCAGGAATTCGAGACC CCTGTAATTCCAGCACTTTGGGAGGCCAAGGTGGGCGGATCACCAGAGGTCAGGAATTCGAGACC A G ATP1B3 Ensembl:ENSG00000069849 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs997733418 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49898,RMVar_hsa_circ_309092,RMVar_hsa_circ_317323 47605 RMVar_ID_47605 Human_SNP_ID_156059195 A-to-I Human chr3 + 141919818 141919818 141919818 AAAATGAGCCTGACGTGGTGGCATGTGCCTGTAATCCCAGCTACTCGGGAGGCTTAGGCAAGAGA AAAATGAGCCTGACGTGGTGGCATGTGCCTGTGATCCCAGCTACTCGGGAGGCTTAGGCAAGAGA A G ATP1B3 Ensembl:ENSG00000069849 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1032979574 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49898,RMVar_hsa_circ_309092,RMVar_hsa_circ_317323 47606 RMVar_ID_47606 Human_SNP_ID_156059349 A-to-I Human chr3 + 141920420 141920420 141920420 ATGGTGGCGCACACTTGTAATCCCAGCTATTCAGGAGGCTGAGACAGGAGAATCGCTTGAACCCG ATGGTGGCGCACACTTGTAATCCCAGCTATTCTGGAGGCTGAGACAGGAGAATCGCTTGAACCCG A T ATP1B3 Ensembl:ENSG00000069849 Protein coding intron GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs527614915 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14651210 RMVar_hsa_circ_49898,RMVar_hsa_circ_309092,RMVar_hsa_circ_317323 47607 RMVar_ID_47607 Human_SNP_ID_156066353 A-to-I Human chr3 - 141945396 141945396 141945396 TGCCAGGCACAGTGGCTCACGCCTGTGATCCCAGCACTTTGGGAGGCCGAGGCGGGCGGATCACC TGCCAGGCACAGTGGCTCACGCCTGTGATCCCGGCACTTTGGGAGGCCGAGGCGGGCGGATCACC T C TFDP2 Ensembl:ENSG00000114126 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1462789372 Functional Loss SNV dbSNP153 33..33 33 - - - 47608 RMVar_ID_47608 Human_SNP_ID_156066676 A-to-I Human chr3 - 141946845 141946845 141946845 TTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGACCACACTGGTCTTGAACTTCTAACCA TTTTGTATTTTTAGTAGAGACAGGGTTTCACCGTGTTGACCACACTGGTCTTGAACTTCTAACCA T C TFDP2 Ensembl:ENSG00000114126 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1478568075 Functional Loss SNV dbSNP153 33..33 33 - - - 47609 RMVar_ID_47609 Human_SNP_ID_156066680 A-to-I Human chr3 - 141946862 141946862 141946862 CACCACGCCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGACCACACTGG CACCACGCCTGGCTAATTTTTGTATTTTTAGTTGAGACAGGGTTTCACCATGTTGACCACACTGG T A TFDP2 Ensembl:ENSG00000114126 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs75102526 Functional Loss SNV dbSNP153 33..33 33 - - - 47610 RMVar_ID_47610 Human_SNP_ID_156066704 A-to-I Human chr3 - 141946941 141946941 141946941 CCACTGCAACCTCTGCCTCCCGGGTTCAAGCGATTCTTCTGCCTCAGCCTCCCAAGTAGTTGGGA CCACTGCAACCTCTGCCTCCCGGGTTCAAGCGGTTCTTCTGCCTCAGCCTCCCAAGTAGTTGGGA T C TFDP2 Ensembl:ENSG00000114126 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1466735908 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7243760,Human_RBP_ID_14987044 47611 RMVar_ID_47611 Human_SNP_ID_156066843 A-to-I Human chr3 - 141947588 141947588 141947588 GAATCTATGCAGTAGAAAAATCATTAGAAAATACAAAAATTAGCCGGGCGTGGTGGCACATGCCT GAATCTATGCAGTAGAAAAATCATTAGAAAATTCAAAAATTAGCCGGGCGTGGTGGCACATGCCT T A TFDP2 Ensembl:ENSG00000114126 Protein coding 3'UTR GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs554715012 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_157363 47612 RMVar_ID_47612 Human_SNP_ID_156067060 A-to-I Human chr3 - 141948496 141948496 141948496 GCTCTGTCGCCAGGCTGGAGTGTAGTGGCGCAATCCCGGCTCACTGCAACCTCTGCCTCCCGGGT GCTCTGTCGCCAGGCTGGAGTGTAGTGGCGCAGTCCCGGCTCACTGCAACCTCTGCCTCCCGGGT T C TFDP2 Ensembl:ENSG00000114126 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1050115060 Functional Loss SNV dbSNP153 33..33 33 - - - 47613 RMVar_ID_47613 Human_SNP_ID_156067534 A-to-I Human chr3 - 141949839 141949839 141949839 CACCACTGCACTCCAGCCTGGGTGACAGAGCAAGACCCTGTCTCAAAAAAAAAAAAAAAAAAAAT CACCACTGCACTCCAGCCTGGGTGACAGAGCAGGACCCTGTCTCAAAAAAAAAAAAAAAAAAAAT T C TFDP2 Ensembl:ENSG00000114126 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1272488900 Functional Loss SNV dbSNP153 33..33 33 - - - 47614 RMVar_ID_47614 Human_SNP_ID_156067552 A-to-I Human chr3 - 141949916 141949916 141949916 GTAGTCCTGGCTACTCAAGAGGCTGAGGTGGGAGGATTGCTTGAGCGCAGGAGGCGGAGGTTGTA GTAGTCCTGGCTACTCAAGAGGCTGAGGTGGGTGGATTGCTTGAGCGCAGGAGGCGGAGGTTGTA T A TFDP2 Ensembl:ENSG00000114126 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1412427266 Functional Loss SNV dbSNP153 33..33 33 - - - 47615 RMVar_ID_47615 Human_SNP_ID_156067558 A-to-I Human chr3 - 141949936 141949936 141949936 GGGTGTGGTGGGGCATGCCTGTAGTCCTGGCTACTCAAGAGGCTGAGGTGGGAGGATTGCTTGAG GGGTGTGGTGGGGCATGCCTGTAGTCCTGGCTGCTCAAGAGGCTGAGGTGGGAGGATTGCTTGAG T C TFDP2 Ensembl:ENSG00000114126 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1382811815 Functional Loss SNV dbSNP153 33..33 33 - - - 47616 RMVar_ID_47616 Human_SNP_ID_156067570 A-to-I Human chr3 - 141949978 141949978 141949978 ACATGACAAAACCCTGTCTCTACAAAAATACAAAAATTAGCTGGGTGTGGTGGGGCATGCCTGTA ACATGACAAAACCCTGTCTCTACAAAAATACACAAATTAGCTGGGTGTGGTGGGGCATGCCTGTA T G TFDP2 Ensembl:ENSG00000114126 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs987018186 Functional Loss SNV dbSNP153 33..33 33 - - - 47617 RMVar_ID_47617 Human_SNP_ID_156069214 A-to-I Human chr3 - 141956868 141956868 141956868 CAGGCTGGAGTGCAGTGGCGCAATCTCTGCTCACTGCAGCCTCGAACTCATGGGCTCAAACGATC CAGGCTGGAGTGCAGTGGCGCAATCTCTGCTCGCTGCAGCCTCGAACTCATGGGCTCAAACGATC T C TFDP2 Ensembl:ENSG00000114126 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910909196 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9569,RMVar_hsa_circ_331888,RMVar_hsa_circ_342672,RMVar_hsa_circ_15989 47618 RMVar_ID_47618 Human_SNP_ID_156075538 A-to-I Human chr3 - 141978288 141978288 141978288 CAGGCTGGAGTTCAGTGGCGCGATCTCGGCTCACTGCAACCTCTGCCTCCCAGGTTCAAGCTATT CAGGCTGGAGTTCAGTGGCGCGATCTCGGCTCGCTGCAACCTCTGCCTCCCAGGTTCAAGCTATT T C TFDP2 Ensembl:ENSG00000114126 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1039527016 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9569,RMVar_hsa_circ_331888,RMVar_hsa_circ_15989,RMVar_hsa_circ_316631,RMVar_hsa_circ_322812,RMVar_hsa_circ_300882,RMVar_hsa_circ_274012,RMVar_hsa_circ_294302,RMVar_hsa_circ_27038,RMVar_hsa_circ_17243,RMVar_hsa_circ_73369,RMVar_hsa_circ_221861,RMVar_hsa_circ_221863,RMVar_hsa_circ_221864,RMVar_hsa_circ_221862,RMVar_hsa_circ_221860,RMVar_hsa_circ_39010,RMVar_hsa_circ_54921,RMVar_hsa_circ_72104,RMVar_hsa_circ_353129,RMVar_hsa_circ_221867,RMVar_hsa_circ_285462,RMVar_hsa_circ_316443,RMVar_hsa_circ_360308,RMVar_hsa_circ_297407,RMVar_hsa_circ_221868 47619 RMVar_ID_47619 Human_SNP_ID_156082742 A-to-I Human chr3 - 142008130 142008130 142008130 CAATTATATCAGCAGCTCTAGGATTGGAACCTAGGAATTGGTATTGTTCATTGTTCCCCAGGTGA CAATTATATCAGCAGCTCTAGGATTGGAACCTGGGAATTGGTATTGTTCATTGTTCCCCAGGTGA T C TFDP2 Ensembl:ENSG00000114126 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1407035053 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9569,RMVar_hsa_circ_322812,RMVar_hsa_circ_300882,RMVar_hsa_circ_17243,RMVar_hsa_circ_39010,RMVar_hsa_circ_298981,RMVar_hsa_circ_297407,RMVar_hsa_circ_339090,RMVar_hsa_circ_304337,RMVar_hsa_circ_221870,RMVar_hsa_circ_348867,RMVar_hsa_circ_221871,RMVar_hsa_circ_297036,RMVar_hsa_circ_317074,RMVar_hsa_circ_221872 47620 RMVar_ID_47620 Human_SNP_ID_156085857 A-to-I Human chr3 - 142020818 142020818 142020818 ACTACACCTGGGTAATTTTATTATTTTTTTGTAGAGATGAGGCCTTACTATGTTGCCCAGGCTGG ACTACACCTGGGTAATTTTATTATTTTTTTGTGGAGATGAGGCCTTACTATGTTGCCCAGGCTGG T C TFDP2 Ensembl:ENSG00000114126 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1475837002 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9569,RMVar_hsa_circ_322812,RMVar_hsa_circ_300882,RMVar_hsa_circ_17243,RMVar_hsa_circ_39010,RMVar_hsa_circ_298981,RMVar_hsa_circ_297407,RMVar_hsa_circ_339090,RMVar_hsa_circ_304337,RMVar_hsa_circ_221870,RMVar_hsa_circ_348867,RMVar_hsa_circ_221871,RMVar_hsa_circ_297036,RMVar_hsa_circ_317074,RMVar_hsa_circ_221872,RMVar_hsa_circ_221873 47621 RMVar_ID_47621 Human_SNP_ID_156086642 A-to-I Human chr3 - 142023976 142023967 142023976 GGGCACATGGCAAAATCCTGTCTCTACAAAAAATACAAAAATTAACTGGGCATGGTGGCACGCAC GGGCACATGGCAAAATCCTGTCTCTACAAAAA_________TTAACTGGGCATGGTGGCACGCAC ATTTTTGTAT A TFDP2 Ensembl:ENSG00000114126 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1273628394 Functional Loss DEL dbSNP153 33..41 33 - - - RMVar_hsa_circ_9569,RMVar_hsa_circ_322812,RMVar_hsa_circ_300882,RMVar_hsa_circ_17243,RMVar_hsa_circ_39010,RMVar_hsa_circ_298981,RMVar_hsa_circ_297407,RMVar_hsa_circ_339090,RMVar_hsa_circ_304337,RMVar_hsa_circ_221870,RMVar_hsa_circ_348867,RMVar_hsa_circ_221871,RMVar_hsa_circ_297036,RMVar_hsa_circ_317074,RMVar_hsa_circ_221872,RMVar_hsa_circ_221873 47622 RMVar_ID_47622 Human_SNP_ID_156086647 A-to-I Human chr3 - 142023976 142023975 142023976 GGGCACATGGCAAAATCCTGTCTCTACAAAAAATACAAAAATTAACTGGGCATGGTGGCACGCAC GGGCACATGGCAAAATCCTGTCTCTACAAAAA_TACAAAAATTAACTGGGCATGGTGGCACGCAC AT A TFDP2 Ensembl:ENSG00000114126 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs147105273 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_9569,RMVar_hsa_circ_322812,RMVar_hsa_circ_300882,RMVar_hsa_circ_17243,RMVar_hsa_circ_39010,RMVar_hsa_circ_298981,RMVar_hsa_circ_297407,RMVar_hsa_circ_339090,RMVar_hsa_circ_304337,RMVar_hsa_circ_221870,RMVar_hsa_circ_348867,RMVar_hsa_circ_221871,RMVar_hsa_circ_297036,RMVar_hsa_circ_317074,RMVar_hsa_circ_221872,RMVar_hsa_circ_221873 47623 RMVar_ID_47623 Human_SNP_ID_156092386 A-to-I Human chr3 - 142047844 142047844 142047844 CCAGCTACTTGGCAGGCTGAGGCAGGAGAATCACTTGAACCCGGGAGGCGGAGGTTGCAGTGAAC CCAGCTACTTGGCAGGCTGAGGCAGGAGAATCGCTTGAACCCGGGAGGCGGAGGTTGCAGTGAAC T C TFDP2 Ensembl:ENSG00000114126 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs201511243 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9569,RMVar_hsa_circ_322812,RMVar_hsa_circ_300882,RMVar_hsa_circ_17243,RMVar_hsa_circ_39010,RMVar_hsa_circ_298981,RMVar_hsa_circ_297407,RMVar_hsa_circ_339090,RMVar_hsa_circ_304337,RMVar_hsa_circ_221870,RMVar_hsa_circ_348867,RMVar_hsa_circ_221871,RMVar_hsa_circ_297036,RMVar_hsa_circ_317074,RMVar_hsa_circ_221872,RMVar_hsa_circ_221873 47624 RMVar_ID_47624 Human_SNP_ID_156102271 A-to-I Human chr3 - 142090671 142090671 142090671 CTGTAATCCCAGCTACTGCGGAGGCTGAGGCAAGAGAATCACTTGAACCCAGGAGGCGGAAGCTG CTGTAATCCCAGCTACTGCGGAGGCTGAGGCAGGAGAATCACTTGAACCCAGGAGGCGGAAGCTG T C TFDP2 Ensembl:ENSG00000114126 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs974912464 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9569,RMVar_hsa_circ_322812,RMVar_hsa_circ_300882,RMVar_hsa_circ_17243,RMVar_hsa_circ_39010,RMVar_hsa_circ_298981,RMVar_hsa_circ_297407,RMVar_hsa_circ_339090,RMVar_hsa_circ_304337,RMVar_hsa_circ_221870,RMVar_hsa_circ_348867,RMVar_hsa_circ_221871,RMVar_hsa_circ_297036,RMVar_hsa_circ_317074,RMVar_hsa_circ_221872,RMVar_hsa_circ_221873,RMVar_hsa_circ_333776 47625 RMVar_ID_47625 Human_SNP_ID_156102868 A-to-I Human chr3 - 142093399 142093399 142093399 TCATCCAGGCTGGAGTGCAGTGGCATGATCTCAGCTCACTGCAACACCTCTGCCTCCCAGGCTCA TCATCCAGGCTGGAGTGCAGTGGCATGATCTCGGCTCACTGCAACACCTCTGCCTCCCAGGCTCA T C TFDP2 Ensembl:ENSG00000114126 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1016804550 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9569,RMVar_hsa_circ_300882,RMVar_hsa_circ_298981,RMVar_hsa_circ_274326,RMVar_hsa_circ_221871,RMVar_hsa_circ_297036,RMVar_hsa_circ_333776,RMVar_hsa_circ_221874,RMVar_hsa_circ_221875 47626 RMVar_ID_47626 Human_SNP_ID_156118326 A-to-I Human chr3 - 142160041 142160041 142160041 GAGTTCAAGACCAGCCTGATCAATATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCC GAGTTCAAGACCAGCCTGATCAATATGGTGAATCCCCATCTCTACTAAAAATACAAAAATTAGCC T A GK5 Ensembl:ENSG00000175066 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1177447342 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_158797 RMVar_hsa_circ_269605 47627 RMVar_ID_47627 Human_SNP_ID_156118521 A-to-I Human chr3 - 142161004 142161004 142161004 TATTTAAAATTTTTGGCCAAGTACAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAG TATTTAAAATTTTTGGCCAAGTACAGTGGCTCGTGCCTGTAATCCCAGCACTTTGGGAGGCTGAG T C GK5 Ensembl:ENSG00000175066 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1211079297 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269605 47628 RMVar_ID_47628 Human_SNP_ID_156118594 A-to-I Human chr3 - 142161229 142161225 142161230 GTGCGTTGTGGCACATGCCTGTAATCCCAGCTAGTCAGGAGGCTGAGGCAGGAGAACCGCTTGAA GTGCGTTGTGGCACATGCCTGTAATCCCAGC_____AGGAGGCTGAGGCAGGAGAACCGCTTGAA TGACTA T GK5 Ensembl:ENSG00000175066 Protein coding 3'UTR GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1178525470 Functional Loss DEL dbSNP153 32..36 33 - - - Human_RBP_ID_25701601 RMVar_hsa_circ_269605 47629 RMVar_ID_47629 Human_SNP_ID_156118610 A-to-I Human chr3 - 142161304 142161304 142161304 GAGGTTAGTAGCTTGAGACCAGCCTGACCAACATGGAGAAACCCCATCTCTATTAAAACTACAAA GAGGTTAGTAGCTTGAGACCAGCCTGACCAACGTGGAGAAACCCCATCTCTATTAAAACTACAAA T C GK5 Ensembl:ENSG00000175066 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1358231417 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269605 47630 RMVar_ID_47630 Human_SNP_ID_156118749 A-to-I Human chr3 - 142161973 142161973 142161973 CAACCTGGCGAATCCCTATCTCTACAAAAAATACACAAATTAGCTGGGTGTGGTGACACACACAT CAACCTGGCGAATCCCTATCTCTACAAAAAATGCACAAATTAGCTGGGTGTGGTGACACACACAT T C GK5 Ensembl:ENSG00000175066 Protein coding 3'UTR GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1341410199 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269605 47631 RMVar_ID_47631 Human_SNP_ID_156118751 A-to-I Human chr3 - 142161988 142161988 142161988 TGAGACCAGCCTGGGCAACCTGGCGAATCCCTATCTCTACAAAAAATACACAAATTAGCTGGGTG TGAGACCAGCCTGGGCAACCTGGCGAATCCCTGTCTCTACAAAAAATACACAAATTAGCTGGGTG T C GK5 Ensembl:ENSG00000175066 Protein coding 3'UTR GSE38233;GSE99789;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29796672,31158229 RNA-Seq:(High) rs1006028264 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269605 47632 RMVar_ID_47632 Human_SNP_ID_156118757 A-to-I Human chr3 - 142162027 142162027 142162027 GGGAGGCCAAGGCAGGCGGATCACTTCAGCTCAGGAGTTTGAGACCAGCCTGGGCAACCTGGCGA GGGAGGCCAAGGCAGGCGGATCACTTCAGCTCGGGAGTTTGAGACCAGCCTGGGCAACCTGGCGA T C GK5 Ensembl:ENSG00000175066 Protein coding 3'UTR GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs1219278043 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269605 47633 RMVar_ID_47633 Human_SNP_ID_156118910 A-to-I Human chr3 - 142162772 142162772 142162772 AGGCTGGTCTCAAACTCCTGACCTTGTGACCCACCCACCTCGGCCTCCCAAAGTGCTAGGATTAC AGGCTGGTCTCAAACTCCTGACCTTGTGACCCCCCCACCTCGGCCTCCCAAAGTGCTAGGATTAC T G GK5 Ensembl:ENSG00000175066 Protein coding 3'UTR GSE38233;GSE99789 cultured B-cells;esophageal squamous carcinoma cells,EC109 - 24183664,29796672 RNA-Seq:(High) rs1212287003 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269605 47634 RMVar_ID_47634 Human_SNP_ID_156118928 A-to-I Human chr3 - 142162833 142162833 142162833 CGTCACTACGCCCAGCTGATTTTTGTATTTTTAGTAGAGACAGGGTTTTACCATGTTGGCCAGGC CGTCACTACGCCCAGCTGATTTTTGTATTTTTGGTAGAGACAGGGTTTTACCATGTTGGCCAGGC T C GK5 Ensembl:ENSG00000175066 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs755568347 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269605 47635 RMVar_ID_47635 Human_SNP_ID_156118930 A-to-I Human chr3 - 142162839 142162839 142162839 GGTATACGTCACTACGCCCAGCTGATTTTTGTATTTTTAGTAGAGACAGGGTTTTACCATGTTGG GGTATACGTCACTACGCCCAGCTGATTTTTGTGTTTTTAGTAGAGACAGGGTTTTACCATGTTGG T C GK5 Ensembl:ENSG00000175066 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs919051218 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269605 47636 RMVar_ID_47636 Human_SNP_ID_156118944 A-to-I Human chr3 - 142162887 142162887 142162887 GGCTCAAGCAGTCCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTTCAGGTATACGTCACTACGC GGCTCAAGCAGTCCTCCTGCCTCAGCCTCCCAGGTAGCTGGGATTTCAGGTATACGTCACTACGC T C GK5 Ensembl:ENSG00000175066 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs919145393 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269605 47637 RMVar_ID_47637 Human_SNP_ID_156118945 A-to-I Human chr3 - 142162887 142162887 142162887 GGCTCAAGCAGTCCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTTCAGGTATACGTCACTACGC GGCTCAAGCAGTCCTCCTGCCTCAGCCTCCCACGTAGCTGGGATTTCAGGTATACGTCACTACGC T G GK5 Ensembl:ENSG00000175066 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs919145393 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269605 47638 RMVar_ID_47638 Human_SNP_ID_156119079 A-to-I Human chr3 - 142163337 142163316 142163338 CTGGGGGGTGGAAGTTGCAGTGAGCCAAGATCATGCCACTGCACTGTAGCCTGGGCAACAGAGCG CTGGGGGGTGGAAGTTGCAGTGAGCCAAGAT______________________GGCAACAGAGCG CCAGGCTACAGTGCAGTGGCATG C GK5 Ensembl:ENSG00000175066 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1436269194 Functional Loss DEL dbSNP153 32..53 33 - - - RMVar_hsa_circ_269605 47639 RMVar_ID_47639 Human_SNP_ID_156119082 A-to-I Human chr3 - 142163332 142163332 142163332 GGGTGGAAGTTGCAGTGAGCCAAGATCATGCCACTGCACTGTAGCCTGGGCAACAGAGCGACACT GGGTGGAAGTTGCAGTGAGCCAAGATCATGCCCCTGCACTGTAGCCTGGGCAACAGAGCGACACT T G GK5 Ensembl:ENSG00000175066 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348507925 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269605 47640 RMVar_ID_47640 Human_SNP_ID_156119103 A-to-I Human chr3 - 142163445 142163445 142163445 CACGGTGAAACCCTGTCTCCACTAAAAATACAAAAATTAGCTGGATGTGGTGGTGCAAGCCTGTA CACGGTGAAACCCTGTCTCCACTAAAAATACAGAAATTAGCTGGATGTGGTGGTGCAAGCCTGTA T C GK5 Ensembl:ENSG00000175066 Protein coding 3'UTR GSE100210;GSE99789 HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 29129909,29796672 RNA-Seq:(High) rs866339187 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269605 47641 RMVar_ID_47641 Human_SNP_ID_156119182 A-to-I Human chr3 - 142163778 142163778 142163778 TTGCCCAGGGTAGTCTTTAATTCCTGGCCTCAAGTGATCCTCCCACCTTGGCCTCCCAAAGTGCT TTGCCCAGGGTAGTCTTTAATTCCTGGCCTCAGGTGATCCTCCCACCTTGGCCTCCCAAAGTGCT T C GK5 Ensembl:ENSG00000175066 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1396737220 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17574404 Human_Splice_Rec_491466 RMVar_hsa_circ_269605 47642 RMVar_ID_47642 Human_SNP_ID_156123586 A-to-I Human chr3 - 142183383 142183383 142183383 AGGCTGAGGTGGGAGGATCACTTGAGTCCAGAAGTTTGAGGCTGCAGTGAGCTGTGATCTTACTG AGGCTGAGGTGGGAGGATCACTTGAGTCCAGACGTTTGAGGCTGCAGTGAGCTGTGATCTTACTG T G GK5 Ensembl:ENSG00000175066 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1483558724 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23718,RMVar_hsa_circ_355183,RMVar_hsa_circ_269605,RMVar_hsa_circ_353115,RMVar_hsa_circ_25112,RMVar_hsa_circ_221879,RMVar_hsa_circ_221877,RMVar_hsa_circ_337234,RMVar_hsa_circ_376046,RMVar_hsa_circ_33709,RMVar_hsa_circ_221878,RMVar_hsa_circ_372689,RMVar_hsa_circ_376883,RMVar_hsa_circ_38615,RMVar_hsa_circ_56094,RMVar_hsa_circ_316310,RMVar_hsa_circ_353714,RMVar_hsa_circ_221884,RMVar_hsa_circ_374424,RMVar_hsa_circ_342204,RMVar_hsa_circ_264900,RMVar_hsa_circ_221886,RMVar_hsa_circ_29115,RMVar_hsa_circ_221887,RMVar_hsa_circ_221885,RMVar_hsa_circ_362151,RMVar_hsa_circ_41355 47643 RMVar_ID_47643 Human_SNP_ID_156123611 A-to-I Human chr3 - 142183475 142183475 142183475 AGAGTAAGACTCCGTCTCAATGAAAAAGAATTAGCTGGATGTGGTGGTGTGCGCCTGTAGTCCTA AGAGTAAGACTCCGTCTCAATGAAAAAGAATTGGCTGGATGTGGTGGTGTGCGCCTGTAGTCCTA T C GK5 Ensembl:ENSG00000175066 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1407639846 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23718,RMVar_hsa_circ_355183,RMVar_hsa_circ_269605,RMVar_hsa_circ_353115,RMVar_hsa_circ_25112,RMVar_hsa_circ_221879,RMVar_hsa_circ_221877,RMVar_hsa_circ_337234,RMVar_hsa_circ_376046,RMVar_hsa_circ_33709,RMVar_hsa_circ_221878,RMVar_hsa_circ_372689,RMVar_hsa_circ_376883,RMVar_hsa_circ_38615,RMVar_hsa_circ_56094,RMVar_hsa_circ_316310,RMVar_hsa_circ_353714,RMVar_hsa_circ_221884,RMVar_hsa_circ_374424,RMVar_hsa_circ_342204,RMVar_hsa_circ_264900,RMVar_hsa_circ_221886,RMVar_hsa_circ_29115,RMVar_hsa_circ_221887,RMVar_hsa_circ_221885,RMVar_hsa_circ_362151,RMVar_hsa_circ_41355 47644 RMVar_ID_47644 Human_SNP_ID_156123676 A-to-I Human chr3 - 142183732 142183732 142183732 GAAATGGCCAGGTGCAGTGGCTCACACCTGCAATCCCAGCACTTTGGGAGGCCGGGGCAGGTGGA GAAATGGCCAGGTGCAGTGGCTCACACCTGCAGTCCCAGCACTTTGGGAGGCCGGGGCAGGTGGA T C GK5 Ensembl:ENSG00000175066 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1294083037 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23718,RMVar_hsa_circ_355183,RMVar_hsa_circ_269605,RMVar_hsa_circ_353115,RMVar_hsa_circ_25112,RMVar_hsa_circ_221879,RMVar_hsa_circ_221877,RMVar_hsa_circ_337234,RMVar_hsa_circ_376046,RMVar_hsa_circ_33709,RMVar_hsa_circ_221878,RMVar_hsa_circ_372689,RMVar_hsa_circ_376883,RMVar_hsa_circ_38615,RMVar_hsa_circ_56094,RMVar_hsa_circ_316310,RMVar_hsa_circ_353714,RMVar_hsa_circ_221884,RMVar_hsa_circ_374424,RMVar_hsa_circ_342204,RMVar_hsa_circ_264900,RMVar_hsa_circ_221886,RMVar_hsa_circ_29115,RMVar_hsa_circ_221887,RMVar_hsa_circ_221885,RMVar_hsa_circ_362151,RMVar_hsa_circ_41355 47645 RMVar_ID_47645 Human_SNP_ID_156123959 A-to-I Human chr3 - 142184720 142184720 142184720 GTGACTCTTCTGCCTCAGCCTCCTGAGTAGCTAGGACTATAGGTGTGCACCACCATGCTTGACTA GTGACTCTTCTGCCTCAGCCTCCTGAGTAGCTGGGACTATAGGTGTGCACCACCATGCTTGACTA T C GK5 Ensembl:ENSG00000175066 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs1255216107 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_491451,Human_Splice_Rec_491485 RMVar_hsa_circ_23718,RMVar_hsa_circ_355183,RMVar_hsa_circ_269605,RMVar_hsa_circ_353115,RMVar_hsa_circ_25112,RMVar_hsa_circ_221879,RMVar_hsa_circ_221877,RMVar_hsa_circ_337234,RMVar_hsa_circ_376046,RMVar_hsa_circ_33709,RMVar_hsa_circ_221878,RMVar_hsa_circ_372689,RMVar_hsa_circ_376883,RMVar_hsa_circ_38615,RMVar_hsa_circ_56094,RMVar_hsa_circ_316310,RMVar_hsa_circ_353714,RMVar_hsa_circ_221884,RMVar_hsa_circ_374424,RMVar_hsa_circ_342204,RMVar_hsa_circ_264900,RMVar_hsa_circ_221886,RMVar_hsa_circ_29115,RMVar_hsa_circ_221887,RMVar_hsa_circ_221885,RMVar_hsa_circ_362151,RMVar_hsa_circ_91738,RMVar_hsa_circ_41355,RMVar_hsa_circ_97686,RMVar_hsa_circ_221889,RMVar_hsa_circ_81547,RMVar_hsa_circ_221890,RMVar_hsa_circ_221888 47646 RMVar_ID_47646 Human_SNP_ID_156123966 A-to-I Human chr3 - 142184754 142184754 142184754 ATGGCTCACTGTGACCTCCGCCTCTCGGGTTCAAGTGACTCTTCTGCCTCAGCCTCCTGAGTAGC ATGGCTCACTGTGACCTCCGCCTCTCGGGTTCGAGTGACTCTTCTGCCTCAGCCTCCTGAGTAGC T C GK5 Ensembl:ENSG00000175066 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1373461481 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_491451,Human_Splice_Rec_491485 RMVar_hsa_circ_23718,RMVar_hsa_circ_355183,RMVar_hsa_circ_269605,RMVar_hsa_circ_353115,RMVar_hsa_circ_25112,RMVar_hsa_circ_221879,RMVar_hsa_circ_221877,RMVar_hsa_circ_337234,RMVar_hsa_circ_376046,RMVar_hsa_circ_33709,RMVar_hsa_circ_221878,RMVar_hsa_circ_372689,RMVar_hsa_circ_376883,RMVar_hsa_circ_38615,RMVar_hsa_circ_56094,RMVar_hsa_circ_316310,RMVar_hsa_circ_353714,RMVar_hsa_circ_221884,RMVar_hsa_circ_374424,RMVar_hsa_circ_342204,RMVar_hsa_circ_264900,RMVar_hsa_circ_221886,RMVar_hsa_circ_29115,RMVar_hsa_circ_221887,RMVar_hsa_circ_221885,RMVar_hsa_circ_362151,RMVar_hsa_circ_91738,RMVar_hsa_circ_41355,RMVar_hsa_circ_97686,RMVar_hsa_circ_221889,RMVar_hsa_circ_81547,RMVar_hsa_circ_221890,RMVar_hsa_circ_221888 47647 RMVar_ID_47647 Human_SNP_ID_156124065 A-to-I Human chr3 - 142185156 142185156 142185156 CTGCCACCTTTGCCTCCCAAAGTGCTGGGACTACAGGCATGAGTCACTGTGCCAAGCCTGTTTTT CTGCCACCTTTGCCTCCCAAAGTGCTGGGACTGCAGGCATGAGTCACTGTGCCAAGCCTGTTTTT T C GK5 Ensembl:ENSG00000175066 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1419865358 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23718,RMVar_hsa_circ_355183,RMVar_hsa_circ_269605,RMVar_hsa_circ_353115,RMVar_hsa_circ_25112,RMVar_hsa_circ_221879,RMVar_hsa_circ_337234,RMVar_hsa_circ_376046,RMVar_hsa_circ_33709,RMVar_hsa_circ_221878,RMVar_hsa_circ_372689,RMVar_hsa_circ_376883,RMVar_hsa_circ_38615,RMVar_hsa_circ_56094,RMVar_hsa_circ_316310,RMVar_hsa_circ_353714,RMVar_hsa_circ_221884,RMVar_hsa_circ_374424,RMVar_hsa_circ_342204,RMVar_hsa_circ_264900,RMVar_hsa_circ_221886,RMVar_hsa_circ_29115,RMVar_hsa_circ_221887,RMVar_hsa_circ_221885,RMVar_hsa_circ_362151,RMVar_hsa_circ_91738,RMVar_hsa_circ_41355,RMVar_hsa_circ_97686,RMVar_hsa_circ_221889,RMVar_hsa_circ_81547,RMVar_hsa_circ_221890,RMVar_hsa_circ_221888 47648 RMVar_ID_47648 Human_SNP_ID_156124066 A-to-I Human chr3 - 142185168 142185168 142185168 GACTGGGGCCTTCTGCCACCTTTGCCTCCCAAAGTGCTGGGACTACAGGCATGAGTCACTGTGCC GACTGGGGCCTTCTGCCACCTTTGCCTCCCAACGTGCTGGGACTACAGGCATGAGTCACTGTGCC T G GK5 Ensembl:ENSG00000175066 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1244852253 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23718,RMVar_hsa_circ_355183,RMVar_hsa_circ_269605,RMVar_hsa_circ_353115,RMVar_hsa_circ_25112,RMVar_hsa_circ_221879,RMVar_hsa_circ_337234,RMVar_hsa_circ_376046,RMVar_hsa_circ_33709,RMVar_hsa_circ_221878,RMVar_hsa_circ_372689,RMVar_hsa_circ_376883,RMVar_hsa_circ_38615,RMVar_hsa_circ_56094,RMVar_hsa_circ_316310,RMVar_hsa_circ_353714,RMVar_hsa_circ_221884,RMVar_hsa_circ_374424,RMVar_hsa_circ_342204,RMVar_hsa_circ_264900,RMVar_hsa_circ_221886,RMVar_hsa_circ_29115,RMVar_hsa_circ_221887,RMVar_hsa_circ_221885,RMVar_hsa_circ_362151,RMVar_hsa_circ_91738,RMVar_hsa_circ_41355,RMVar_hsa_circ_97686,RMVar_hsa_circ_221889,RMVar_hsa_circ_81547,RMVar_hsa_circ_221890,RMVar_hsa_circ_221888 47649 RMVar_ID_47649 Human_SNP_ID_156124111 A-to-I Human chr3 - 142185409 142185409 142185409 TGCCATTTTTGATTTTTTTTTTTTTTTTTGAGACAGGGTCTCACTCTGTCACTCAGGCTGGAGTG TGCCATTTTTGATTTTTTTTTTTTTTTTTGAGGCAGGGTCTCACTCTGTCACTCAGGCTGGAGTG T C GK5 Ensembl:ENSG00000175066 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1423149022 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23718,RMVar_hsa_circ_355183,RMVar_hsa_circ_269605,RMVar_hsa_circ_353115,RMVar_hsa_circ_25112,RMVar_hsa_circ_221879,RMVar_hsa_circ_337234,RMVar_hsa_circ_376046,RMVar_hsa_circ_33709,RMVar_hsa_circ_221878,RMVar_hsa_circ_372689,RMVar_hsa_circ_376883,RMVar_hsa_circ_38615,RMVar_hsa_circ_56094,RMVar_hsa_circ_316310,RMVar_hsa_circ_353714,RMVar_hsa_circ_221884,RMVar_hsa_circ_374424,RMVar_hsa_circ_342204,RMVar_hsa_circ_264900,RMVar_hsa_circ_221886,RMVar_hsa_circ_29115,RMVar_hsa_circ_221887,RMVar_hsa_circ_221885,RMVar_hsa_circ_362151,RMVar_hsa_circ_91738,RMVar_hsa_circ_41355,RMVar_hsa_circ_97686,RMVar_hsa_circ_221889,RMVar_hsa_circ_81547,RMVar_hsa_circ_221890,RMVar_hsa_circ_221888 47650 RMVar_ID_47650 Human_SNP_ID_156128419 A-to-I Human chr3 - 142204221 142204221 142204221 TTGAGGCCAGAAGTTCAAGACCAGCTTGGGCAACATGGTAAGACCTCATCTCTACAAATAATGCA TTGAGGCCAGAAGTTCAAGACCAGCTTGGGCAGCATGGTAAGACCTCATCTCTACAAATAATGCA T C GK5 Ensembl:ENSG00000175066 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900895379 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_491551,Human_Splice_Rec_491568 RMVar_hsa_circ_23718,RMVar_hsa_circ_269605,RMVar_hsa_circ_25112,RMVar_hsa_circ_38615,RMVar_hsa_circ_2695,RMVar_hsa_circ_56094,RMVar_hsa_circ_353714,RMVar_hsa_circ_374424,RMVar_hsa_circ_221886,RMVar_hsa_circ_221887,RMVar_hsa_circ_91738,RMVar_hsa_circ_221890,RMVar_hsa_circ_54832,RMVar_hsa_circ_221894,RMVar_hsa_circ_63673,RMVar_hsa_circ_325178,RMVar_hsa_circ_304827,RMVar_hsa_circ_281486,RMVar_hsa_circ_221896,RMVar_hsa_circ_221895 47651 RMVar_ID_47651 Human_SNP_ID_156128433 A-to-I Human chr3 - 142204290 142204290 142204290 TATCATTACAGGCATGATGGCTCGCGCCTGTAATCTCAACACTTTGGAAGGCTGAGGCAGGGGGA TATCATTACAGGCATGATGGCTCGCGCCTGTAGTCTCAACACTTTGGAAGGCTGAGGCAGGGGGA T C GK5 Ensembl:ENSG00000175066 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs952091937 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_491551,Human_Splice_Rec_491568 RMVar_hsa_circ_23718,RMVar_hsa_circ_269605,RMVar_hsa_circ_25112,RMVar_hsa_circ_38615,RMVar_hsa_circ_2695,RMVar_hsa_circ_56094,RMVar_hsa_circ_353714,RMVar_hsa_circ_374424,RMVar_hsa_circ_221886,RMVar_hsa_circ_221887,RMVar_hsa_circ_91738,RMVar_hsa_circ_221890,RMVar_hsa_circ_54832,RMVar_hsa_circ_221894,RMVar_hsa_circ_63673,RMVar_hsa_circ_325178,RMVar_hsa_circ_304827,RMVar_hsa_circ_281486,RMVar_hsa_circ_221896,RMVar_hsa_circ_221895 47652 RMVar_ID_47652 Human_SNP_ID_156154585 A-to-I Human chr3 - 142313883 142313883 142313883 CAAGTTAAAGTGCAGTGACATGATCTTGGCTCACTGCAACCTCCACCTCCCAGGCTCAAGCAATC CAAGTTAAAGTGCAGTGACATGATCTTGGCTCTCTGCAACCTCCACCTCCCAGGCTCAAGCAATC T A XRN1 Ensembl:ENSG00000114127 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1305617759 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14480,RMVar_hsa_circ_119525,RMVar_hsa_circ_102364,RMVar_hsa_circ_221900,RMVar_hsa_circ_77025,RMVar_hsa_circ_221901,RMVar_hsa_circ_221899,RMVar_hsa_circ_301721,RMVar_hsa_circ_53111,RMVar_hsa_circ_99565,RMVar_hsa_circ_221902,RMVar_hsa_circ_221903 47653 RMVar_ID_47653 Human_SNP_ID_156154586 A-to-I Human chr3 - 142313883 142313883 142313883 CAAGTTAAAGTGCAGTGACATGATCTTGGCTCACTGCAACCTCCACCTCCCAGGCTCAAGCAATC CAAGTTAAAGTGCAGTGACATGATCTTGGCTCGCTGCAACCTCCACCTCCCAGGCTCAAGCAATC T C XRN1 Ensembl:ENSG00000114127 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1305617759 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14480,RMVar_hsa_circ_119525,RMVar_hsa_circ_102364,RMVar_hsa_circ_221900,RMVar_hsa_circ_77025,RMVar_hsa_circ_221901,RMVar_hsa_circ_221899,RMVar_hsa_circ_301721,RMVar_hsa_circ_53111,RMVar_hsa_circ_99565,RMVar_hsa_circ_221902,RMVar_hsa_circ_221903 47654 RMVar_ID_47654 Human_SNP_ID_156159022 A-to-I Human chr3 - 142332009 142332009 142332009 AACTTTGGGAAGCTGAGGCAGGCGGATCTCTTAAGCTCAGGAGTTCAAGACCAGCCTGGGCAACA AACTTTGGGAAGCTGAGGCAGGCGGATCTCTTCAGCTCAGGAGTTCAAGACCAGCCTGGGCAACA T G XRN1 Ensembl:ENSG00000114127 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1190066789 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14480,RMVar_hsa_circ_221900,RMVar_hsa_circ_77025,RMVar_hsa_circ_5015,RMVar_hsa_circ_59144,RMVar_hsa_circ_73655,RMVar_hsa_circ_126163,RMVar_hsa_circ_356859,RMVar_hsa_circ_83714,RMVar_hsa_circ_221904,RMVar_hsa_circ_330160,RMVar_hsa_circ_351097,RMVar_hsa_circ_93939,RMVar_hsa_circ_77883,RMVar_hsa_circ_32536,RMVar_hsa_circ_37060,RMVar_hsa_circ_23456,RMVar_hsa_circ_221906,RMVar_hsa_circ_221908,RMVar_hsa_circ_221909,RMVar_hsa_circ_221907 47655 RMVar_ID_47655 Human_SNP_ID_156187636 A-to-I Human chr3 + 142450494 142450494 142450494 TCACTTAATGAGGTCCACTAAAGAGAGAGTTCATCAGGATCCTTGTGAGGCTATTTCTCATATCC TCACTTAATGAGGTCCACTAAAGAGAGAGTTCGTCAGGATCCTTGTGAGGCTATTTCTCATATCC A G AC109992.1 Ensembl:ENSG00000242479 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1193498761 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17405907 47656 RMVar_ID_47656 Human_SNP_ID_156187647 A-to-I Human chr3 + 142450521 142450520 142450522 AGTTCATCAGGATCCTTGTGAGGCTATTTCTCATATCCAGAAAATCAGATCAAGGGAAGTACCCT AGTTCATCAGGATCCTTGTGAGGCTATTTCTC__ATCCAGAAAATCAGATCAAGGGAAGTACCCT CAT C AC109992.1 Ensembl:ENSG00000242479 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1249854227 Functional Loss DEL dbSNP153 33..34 33 - - - 47657 RMVar_ID_47657 Human_SNP_ID_156187648 A-to-I Human chr3 + 142450521 142450521 142450521 AGTTCATCAGGATCCTTGTGAGGCTATTTCTCATATCCAGAAAATCAGATCAAGGGAAGTACCCT AGTTCATCAGGATCCTTGTGAGGCTATTTCTCGTATCCAGAAAATCAGATCAAGGGAAGTACCCT A G AC109992.1 Ensembl:ENSG00000242479 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1207892889 Functional Loss SNV dbSNP153 33..33 33 - - - 47658 RMVar_ID_47658 Human_SNP_ID_156195192 A-to-I Human chr3 - 142482775 142482775 142482775 GAGGCAGGAGTGCAGTACAATCATAGCTAACTATGACCTTGAACTCTGGGCTCAAGTGATCCTCC GAGGCAGGAGTGCAGTACAATCATAGCTAACTGTGACCTTGAACTCTGGGCTCAAGTGATCCTCC T C ATR Ensembl:ENSG00000175054 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978928533 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_774,RMVar_hsa_circ_80440,RMVar_hsa_circ_305477,RMVar_hsa_circ_337707,RMVar_hsa_circ_268537,RMVar_hsa_circ_346058,RMVar_hsa_circ_221941,RMVar_hsa_circ_221940,RMVar_hsa_circ_118853,RMVar_hsa_circ_116041,RMVar_hsa_circ_9512,RMVar_hsa_circ_312020,RMVar_hsa_circ_7513,RMVar_hsa_circ_221943,RMVar_hsa_circ_221944,RMVar_hsa_circ_56994,RMVar_hsa_circ_298868,RMVar_hsa_circ_378700,RMVar_hsa_circ_269638,RMVar_hsa_circ_370402,RMVar_hsa_circ_221945,RMVar_hsa_circ_368038,RMVar_hsa_circ_341915,RMVar_hsa_circ_50596,RMVar_hsa_circ_120654,RMVar_hsa_circ_63219,RMVar_hsa_circ_33257,RMVar_hsa_circ_221946,RMVar_hsa_circ_221947,RMVar_hsa_circ_114937,RMVar_hsa_circ_33977,RMVar_hsa_circ_221951,RMVar_hsa_circ_221952,RMVar_hsa_circ_280654,RMVar_hsa_circ_221954,RMVar_hsa_circ_221953,RMVar_hsa_circ_132,RMVar_hsa_circ_109015 47659 RMVar_ID_47659 Human_SNP_ID_156196158 A-to-I Human chr3 - 142486851 142486851 142486851 TGGGCCTCCCAAAGTGCTGGGATTACAAGCATAAGCCATCTTGCCCAGCCAATAATAATAATTAT TGGGCCTCCCAAAGTGCTGGGATTACAAGCATCAGCCATCTTGCCCAGCCAATAATAATAATTAT T G ATR Ensembl:ENSG00000175054 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215382853 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80440,RMVar_hsa_circ_305477,RMVar_hsa_circ_337707,RMVar_hsa_circ_268537,RMVar_hsa_circ_346058,RMVar_hsa_circ_221941,RMVar_hsa_circ_221940,RMVar_hsa_circ_118853,RMVar_hsa_circ_116041,RMVar_hsa_circ_9512,RMVar_hsa_circ_312020,RMVar_hsa_circ_7513,RMVar_hsa_circ_221943,RMVar_hsa_circ_221944,RMVar_hsa_circ_378700,RMVar_hsa_circ_269638,RMVar_hsa_circ_370402,RMVar_hsa_circ_221945,RMVar_hsa_circ_341915,RMVar_hsa_circ_50596,RMVar_hsa_circ_120654,RMVar_hsa_circ_63219,RMVar_hsa_circ_33257,RMVar_hsa_circ_221946,RMVar_hsa_circ_221947,RMVar_hsa_circ_114937,RMVar_hsa_circ_33977,RMVar_hsa_circ_221951,RMVar_hsa_circ_221952,RMVar_hsa_circ_280654,RMVar_hsa_circ_56898,RMVar_hsa_circ_221954,RMVar_hsa_circ_221953,RMVar_hsa_circ_132,RMVar_hsa_circ_109015,RMVar_hsa_circ_107476,RMVar_hsa_circ_298007,RMVar_hsa_circ_341053,RMVar_hsa_circ_78247,RMVar_hsa_circ_221956,RMVar_hsa_circ_45461,RMVar_hsa_circ_221957,RMVar_hsa_circ_221955 47660 RMVar_ID_47660 Human_SNP_ID_156196656 A-to-I Human chr3 - 142489194 142489194 142489194 AAGTAGCTGGGACTACAGGCACATGCCACCACACCCAGCTAATTTTTTATTTTGTGGAGATAGGG AAGTAGCTGGGACTACAGGCACATGCCACCACGCCCAGCTAATTTTTTATTTTGTGGAGATAGGG T C ATR Ensembl:ENSG00000175054 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1000454551 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80440,RMVar_hsa_circ_305477,RMVar_hsa_circ_337707,RMVar_hsa_circ_268537,RMVar_hsa_circ_346058,RMVar_hsa_circ_221941,RMVar_hsa_circ_221940,RMVar_hsa_circ_118853,RMVar_hsa_circ_116041,RMVar_hsa_circ_9512,RMVar_hsa_circ_312020,RMVar_hsa_circ_7513,RMVar_hsa_circ_221943,RMVar_hsa_circ_221944,RMVar_hsa_circ_378700,RMVar_hsa_circ_269638,RMVar_hsa_circ_370402,RMVar_hsa_circ_221945,RMVar_hsa_circ_341915,RMVar_hsa_circ_50596,RMVar_hsa_circ_120654,RMVar_hsa_circ_63219,RMVar_hsa_circ_33257,RMVar_hsa_circ_221946,RMVar_hsa_circ_221947,RMVar_hsa_circ_114937,RMVar_hsa_circ_33977,RMVar_hsa_circ_221951,RMVar_hsa_circ_221952,RMVar_hsa_circ_280654,RMVar_hsa_circ_56898,RMVar_hsa_circ_221954,RMVar_hsa_circ_221953,RMVar_hsa_circ_132,RMVar_hsa_circ_109015,RMVar_hsa_circ_107476,RMVar_hsa_circ_298007,RMVar_hsa_circ_341053,RMVar_hsa_circ_78247,RMVar_hsa_circ_221956,RMVar_hsa_circ_45461,RMVar_hsa_circ_221957,RMVar_hsa_circ_221955 47661 RMVar_ID_47661 Human_SNP_ID_156253306 A-to-I Human chr3 + 142733391 142733391 142733391 AAAATTAGCCGGGCGTGGTGGCAGCTGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA AAAATTAGCCGGGCGTGGTGGCAGCTGCCTGTGATCCCAGCTACTCAGGAGGCTGAGGCAGGAGA A G TRPC1 Ensembl:ENSG00000144935 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs960406003 Functional Loss SNV dbSNP153 33..33 33 - - - 47662 RMVar_ID_47662 Human_SNP_ID_156253309 A-to-I Human chr3 + 142733405 142733405 142733405 GTGGTGGCAGCTGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACCCA GTGGTGGCAGCTGCCTGTAATCCCAGCTACTCTGGAGGCTGAGGCAGGAGAATCGCTTGAACCCA A T TRPC1 Ensembl:ENSG00000144935 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs112468075 Functional Loss SNV dbSNP153 33..33 33 - - - 47663 RMVar_ID_47663 Human_SNP_ID_156255927 A-to-I Human chr3 + 142745990 142745990 142745990 TGTTGGCCAGTCTGGTCTGGAACTCTTGACCTAAGGTGATCTACCCTTCTCGGCCTCCCAAAGTG TGTTGGCCAGTCTGGTCTGGAACTCTTGACCTGAGGTGATCTACCCTTCTCGGCCTCCCAAAGTG A G TRPC1 Ensembl:ENSG00000144935 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1168706031 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_222001,RMVar_hsa_circ_222002,RMVar_hsa_circ_15337,RMVar_hsa_circ_271627,RMVar_hsa_circ_301377,RMVar_hsa_circ_319276,RMVar_hsa_circ_341883,RMVar_hsa_circ_222003,RMVar_hsa_circ_348022,RMVar_hsa_circ_314544,RMVar_hsa_circ_278001,RMVar_hsa_circ_299981,RMVar_hsa_circ_274832,RMVar_hsa_circ_222007,RMVar_hsa_circ_222009,RMVar_hsa_circ_222010,RMVar_hsa_circ_222008,RMVar_hsa_circ_222005,RMVar_hsa_circ_222006,RMVar_hsa_circ_222004,RMVar_hsa_circ_320741,RMVar_hsa_circ_332492,RMVar_hsa_circ_315322,RMVar_hsa_circ_222012,RMVar_hsa_circ_222013 47664 RMVar_ID_47664 Human_SNP_ID_156273527 A-to-I Human chr3 - 142827250 142827250 142827250 GGCCACGAGTATGGGATGTGGCCATGAACCCTATGGAGCATCCTTTTGGAGGTGGCAACCACCAG GGCCACGAGTATGGGATGTGGCCATGAACCCTGTGGAGCATCCTTTTGGAGGTGGCAACCACCAG T C AC021074.1,PCOLCE2 Ensembl:ENSG00000240950,Ensembl:ENSG00000163710 Pseudogene,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879118893 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18517143 RMVar_hsa_circ_222032,RMVar_hsa_circ_373571 47665 RMVar_ID_47665 Human_SNP_ID_156273532 A-to-I Human chr3 - 142827267 142827267 142827267 GGCAAAGAGGAACTGGTGGCCACGAGTATGGGATGTGGCCATGAACCCTATGGAGCATCCTTTTG GGCAAAGAGGAACTGGTGGCCACGAGTATGGGGTGTGGCCATGAACCCTATGGAGCATCCTTTTG T C AC021074.1,PCOLCE2 Ensembl:ENSG00000240950,Ensembl:ENSG00000163710 Pseudogene,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878919236 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1878277,Human_miRNA_ID_1897178 RMVar_hsa_circ_222032,RMVar_hsa_circ_373571 47666 RMVar_ID_47666 Human_SNP_ID_156316887 A-to-I Human chr3 + 143008929 143008929 143008929 ACTACAGGCGCCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCAGGTTTGGCCAGG ACTACAGGCGCCTGGCTAATTTTTGTATTTTTGGTAGAGATGGGGTTTCACCAGGTTTGGCCAGG A G U2SURP Ensembl:ENSG00000163714 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886730527 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25702781 47667 RMVar_ID_47667 Human_SNP_ID_156325673 A-to-I Human chr3 + 143043788 143043788 143043788 GTACTGTGAGAAATCCATTTTTTTTTTTTTTGAGATGGAGTCTCGCAGTGTCACCCAGGCTGGAG GTACTGTGAGAAATCCATTTTTTTTTTTTTTGTGATGGAGTCTCGCAGTGTCACCCAGGCTGGAG A T U2SURP Ensembl:ENSG00000163714 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1433428700 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81353,RMVar_hsa_circ_74442,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 47668 RMVar_ID_47668 Human_SNP_ID_156972885 A-to-I Human chr3 + 145684966 145684966 145684966 TCGAAGAAGGAACCTACTCACTGCCCAAGAGCAAATTCACTGTGCCTTACCTGGAGCTGCCCAGC TCGAAGAAGGAACCTACTCACTGCCCAAGAGCGAATTCACTGTGCCTTACCTGGAGCTGCCCAGC A G GM2AP1 Ensembl:ENSG00000241695 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1379315623 Functional Loss SNV dbSNP153 33..33 33 - - - 47669 RMVar_ID_47669 Human_SNP_ID_157185844 A-to-I Human chr3 - 146542266 146542266 146542266 GGGTGAGTGGGTTGGTGGAGGGCATTATAGACAGAGGGAACCTCACAGGTAGAAGTCCTGGGCTG GGGTGAGTGGGTTGGTGGAGGGCATTATAGACGGAGGGAACCTCACAGGTAGAAGTCCTGGGCTG T C PLSCR1 Ensembl:ENSG00000188313 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1283131592 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17573862 47670 RMVar_ID_47670 Human_SNP_ID_157185849 A-to-I Human chr3 - 146542293 146542293 146542293 CTCAAATCAACTAGTCTATAGACGTGTGGGTGAGTGGGTTGGTGGAGGGCATTATAGACAGAGGG CTCAAATCAACTAGTCTATAGACGTGTGGGTGCGTGGGTTGGTGGAGGGCATTATAGACAGAGGG T G PLSCR1 Ensembl:ENSG00000188313 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1183648116 Functional Loss SNV dbSNP153 33..33 33 - - - 47671 RMVar_ID_47671 Human_SNP_ID_157186012 A-to-I Human chr3 - 146543102 146543102 146543102 AGCTCAGGAATTCTACCTATGGAGTTCCCTCTATCTATGATGCCCTCCAACACCCCACCCACCAT AGCTCAGGAATTCTACCTATGGAGTTCCCTCTGTCTATGATGCCCTCCAACACCCCACCCACCAT T C PLSCR1 Ensembl:ENSG00000188313 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs540841569 Functional Loss SNV dbSNP153 33..33 33 - - - 47672 RMVar_ID_47672 Human_SNP_ID_157186019 A-to-I Human chr3 - 146543120 146543120 146543120 AATGAGGGACGTTCCTCCAGCTCAGGAATTCTACCTATGGAGTTCCCTCTATCTATGATGCCCTC AATGAGGGACGTTCCTCCAGCTCAGGAATTCTGCCTATGGAGTTCCCTCTATCTATGATGCCCTC T C PLSCR1 Ensembl:ENSG00000188313 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1199290112 Functional Loss SNV dbSNP153 33..33 33 - - - 47673 RMVar_ID_47673 Human_SNP_ID_157797079 A-to-I Human chr3 + 149012873 149012873 149012873 TTGAGACGGAATCTTGCTCTGTTGCCTAGGCTAGAGTGCAGTGGTAGAATCACGACTCACTATAG TTGAGACGGAATCTTGCTCTGTTGCCTAGGCTGGAGTGCAGTGGTAGAATCACGACTCACTATAG A G GYG1 Ensembl:ENSG00000163754 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1173132914 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14662748 47674 RMVar_ID_47674 Human_SNP_ID_157798469 A-to-I Human chr3 + 149017874 149017874 149017874 AACTCAGGCAATTCTCCCGCCTCGGCCTCCCAAAGTGCTAGGATTACAGGTGTGAGCCACCACGC AACTCAGGCAATTCTCCCGCCTCGGCCTCCCAGAGTGCTAGGATTACAGGTGTGAGCCACCACGC A G GYG1 Ensembl:ENSG00000163754 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs910103801 Functional Loss SNV dbSNP153 33..33 33 - - - 47675 RMVar_ID_47675 Human_SNP_ID_157809202 A-to-I Human chr3 - 149061670 149061670 149061670 CACCACACCTGGCTAGTTTTTGTATTTTTAGTAGAAACGGGGTTTCACCATGTTAGCCAGTCTGG CACCACACCTGGCTAGTTTTTGTATTTTTAGTGGAAACGGGGTTTCACCATGTTAGCCAGTCTGG T C HLTF Ensembl:ENSG00000071794 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs952960692 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_52103,RMVar_hsa_circ_62356,RMVar_hsa_circ_319475,RMVar_hsa_circ_5288,RMVar_hsa_circ_3676,RMVar_hsa_circ_12753,RMVar_hsa_circ_27003,RMVar_hsa_circ_222089,RMVar_hsa_circ_110028,RMVar_hsa_circ_222090,RMVar_hsa_circ_94078,RMVar_hsa_circ_115802,RMVar_hsa_circ_60920,RMVar_hsa_circ_20275,RMVar_hsa_circ_222094,RMVar_hsa_circ_222092,RMVar_hsa_circ_222093,RMVar_hsa_circ_222099,RMVar_hsa_circ_222091,RMVar_hsa_circ_307765,RMVar_hsa_circ_265978,RMVar_hsa_circ_275044,RMVar_hsa_circ_8400,RMVar_hsa_circ_33244,RMVar_hsa_circ_278161,RMVar_hsa_circ_222101,RMVar_hsa_circ_297816,RMVar_hsa_circ_273819,RMVar_hsa_circ_10232,RMVar_hsa_circ_222102,RMVar_hsa_circ_222103 47676 RMVar_ID_47676 Human_SNP_ID_157810277 A-to-I Human chr3 - 149066149 149066149 149066149 TCAGTTACTTGGGAGGCTGAGGCAGGAGAATCACTTGAACTCAGGAGGTAGAGGTTTCAATGAGC TCAGTTACTTGGGAGGCTGAGGCAGGAGAATCCCTTGAACTCAGGAGGTAGAGGTTTCAATGAGC T G HLTF Ensembl:ENSG00000071794 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934341883 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_52103,RMVar_hsa_circ_319475,RMVar_hsa_circ_5288,RMVar_hsa_circ_3676,RMVar_hsa_circ_27003,RMVar_hsa_circ_222089,RMVar_hsa_circ_94078,RMVar_hsa_circ_115802,RMVar_hsa_circ_222092,RMVar_hsa_circ_222093,RMVar_hsa_circ_222099,RMVar_hsa_circ_222091,RMVar_hsa_circ_307765,RMVar_hsa_circ_265978,RMVar_hsa_circ_275044,RMVar_hsa_circ_278161,RMVar_hsa_circ_222101,RMVar_hsa_circ_273819,RMVar_hsa_circ_10232,RMVar_hsa_circ_19780,RMVar_hsa_circ_222102,RMVar_hsa_circ_299774,RMVar_hsa_circ_310515,RMVar_hsa_circ_27925,RMVar_hsa_circ_222106,RMVar_hsa_circ_5393,RMVar_hsa_circ_222107 47677 RMVar_ID_47677 Human_SNP_ID_157810296 A-to-I Human chr3 - 149066259 149066259 149066259 GGCAGATCACCTGAGGTTAGGAGTTCAAGACCAGTCTGACCAACATGATGAAGCCCTGTCTCTAC GGCAGATCACCTGAGGTTAGGAGTTCAAGACCGGTCTGACCAACATGATGAAGCCCTGTCTCTAC T C HLTF Ensembl:ENSG00000071794 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1313592551 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_52103,RMVar_hsa_circ_319475,RMVar_hsa_circ_5288,RMVar_hsa_circ_3676,RMVar_hsa_circ_27003,RMVar_hsa_circ_222089,RMVar_hsa_circ_94078,RMVar_hsa_circ_115802,RMVar_hsa_circ_222092,RMVar_hsa_circ_222093,RMVar_hsa_circ_222099,RMVar_hsa_circ_222091,RMVar_hsa_circ_307765,RMVar_hsa_circ_265978,RMVar_hsa_circ_275044,RMVar_hsa_circ_278161,RMVar_hsa_circ_222101,RMVar_hsa_circ_273819,RMVar_hsa_circ_10232,RMVar_hsa_circ_19780,RMVar_hsa_circ_222102,RMVar_hsa_circ_299774,RMVar_hsa_circ_310515,RMVar_hsa_circ_27925,RMVar_hsa_circ_222106,RMVar_hsa_circ_5393,RMVar_hsa_circ_222107 47678 RMVar_ID_47678 Human_SNP_ID_157810603 A-to-I Human chr3 - 149067571 149067571 149067571 TGGAGCCCAGGAGTTTGAGCCTATGGTCAGCTATGATTGCACTATTGCACTCCACCTTCAGTGAC TGGAGCCCAGGAGTTTGAGCCTATGGTCAGCTGTGATTGCACTATTGCACTCCACCTTCAGTGAC T C HLTF Ensembl:ENSG00000071794 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1317722959 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_52103,RMVar_hsa_circ_319475,RMVar_hsa_circ_5288,RMVar_hsa_circ_3676,RMVar_hsa_circ_27003,RMVar_hsa_circ_222089,RMVar_hsa_circ_94078,RMVar_hsa_circ_115802,RMVar_hsa_circ_222092,RMVar_hsa_circ_222093,RMVar_hsa_circ_222099,RMVar_hsa_circ_222091,RMVar_hsa_circ_307765,RMVar_hsa_circ_265978,RMVar_hsa_circ_275044,RMVar_hsa_circ_278161,RMVar_hsa_circ_222101,RMVar_hsa_circ_273819,RMVar_hsa_circ_10232,RMVar_hsa_circ_19780,RMVar_hsa_circ_222102,RMVar_hsa_circ_299774,RMVar_hsa_circ_310515,RMVar_hsa_circ_27925,RMVar_hsa_circ_222106,RMVar_hsa_circ_5393,RMVar_hsa_circ_222107 47679 RMVar_ID_47679 Human_SNP_ID_157810719 A-to-I Human chr3 - 149068035 149068035 149068035 ACGTTTTCAGACAAGGTGTGGCTCTGTTGCCCAGGCTGGAGTGCAGTGGCGCAATCTCAGCTCAC ACGTTTTCAGACAAGGTGTGGCTCTGTTGCCCGGGCTGGAGTGCAGTGGCGCAATCTCAGCTCAC T C HLTF Ensembl:ENSG00000071794 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,frontal_cortex - 29129909,30559470 RNA-Seq:(High) rs1419655766 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_52103,RMVar_hsa_circ_319475,RMVar_hsa_circ_5288,RMVar_hsa_circ_3676,RMVar_hsa_circ_27003,RMVar_hsa_circ_222089,RMVar_hsa_circ_94078,RMVar_hsa_circ_115802,RMVar_hsa_circ_222092,RMVar_hsa_circ_222093,RMVar_hsa_circ_222099,RMVar_hsa_circ_222091,RMVar_hsa_circ_307765,RMVar_hsa_circ_265978,RMVar_hsa_circ_275044,RMVar_hsa_circ_278161,RMVar_hsa_circ_222101,RMVar_hsa_circ_273819,RMVar_hsa_circ_10232,RMVar_hsa_circ_19780,RMVar_hsa_circ_222102,RMVar_hsa_circ_299774,RMVar_hsa_circ_310515,RMVar_hsa_circ_27925,RMVar_hsa_circ_222106,RMVar_hsa_circ_5393,RMVar_hsa_circ_222107 47680 RMVar_ID_47680 Human_SNP_ID_157832930 A-to-I Human chr3 + 149153619 149153619 149153619 CTTTTGACTAAAGCAGAACCTGAAGCCATTCCAGAGAGAAGACAGTCACCCAAGAGGCTTCTGTA CTTTTGACTAAAGCAGAACCTGAAGCCATTCCGGAGAGAAGACAGTCACCCAAGAGGCTTCTGTA A G HPS3 Ensembl:ENSG00000163755 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs144353823 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_592022,Human_RBP_ID_14664194 Human_Splice_Rec_494963,Human_Splice_Rec_494995 Human_miRNA_ID_31825,Human_miRNA_ID_553678,Human_miRNA_ID_2036566,Human_miRNA_ID_2347268,Human_miRNA_ID_3116379 RMVar_hsa_circ_13397,RMVar_hsa_circ_14550,RMVar_hsa_circ_57308,RMVar_hsa_circ_338693,RMVar_hsa_circ_354180,RMVar_hsa_circ_69237,RMVar_hsa_circ_222116,RMVar_hsa_circ_42986,RMVar_hsa_circ_53076,RMVar_hsa_circ_222117,RMVar_hsa_circ_30172,RMVar_hsa_circ_313595,RMVar_hsa_circ_29995,RMVar_hsa_circ_222120 47681 RMVar_ID_47681 Human_SNP_ID_157935129 A-to-I Human chr3 - 149568151 149568151 149568151 GAACTCCTGACCTCAGGCAATCCGCCCATCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG GAACTCCTGACCTCAGGCAATCCGCCCATCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG T C WWTR1 Ensembl:ENSG00000018408 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs574805258 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25146,RMVar_hsa_circ_324600 47682 RMVar_ID_47682 Human_SNP_ID_157952114 A-to-I Human chr3 - 149639480 149639480 149639480 GTAACTTTAGGTTGTCGTGGCTCACACTTATAATCCCAGAACTTTGGGAGGCTGAGGCAGGAGAA GTAACTTTAGGTTGTCGTGGCTCACACTTATAGTCCCAGAACTTTGGGAGGCTGAGGCAGGAGAA T C WWTR1 Ensembl:ENSG00000018408 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1004527555 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5637,RMVar_hsa_circ_107241,RMVar_hsa_circ_222130 47683 RMVar_ID_47683 Human_SNP_ID_157952118 A-to-I Human chr3 - 149639487 149639487 149639487 AGAAGAGGTAACTTTAGGTTGTCGTGGCTCACACTTATAATCCCAGAACTTTGGGAGGCTGAGGC AGAAGAGGTAACTTTAGGTTGTCGTGGCTCACGCTTATAATCCCAGAACTTTGGGAGGCTGAGGC T C WWTR1 Ensembl:ENSG00000018408 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1212774613 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5637,RMVar_hsa_circ_107241,RMVar_hsa_circ_222130 47684 RMVar_ID_47684 Human_SNP_ID_157953436 A-to-I Human chr3 - 149644990 149644990 149644990 AAATTAGTTGGGCATGGTGGCGTGTACCTGTAATCCCAGTTACCTGGGAGGCTGAGACACGAGAA AAATTAGTTGGGCATGGTGGCGTGTACCTGTACTCCCAGTTACCTGGGAGGCTGAGACACGAGAA T G WWTR1 Ensembl:ENSG00000018408 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749358145 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5637,RMVar_hsa_circ_107241,RMVar_hsa_circ_222130 47685 RMVar_ID_47685 Human_SNP_ID_157970889 A-to-I Human chr3 - 149716914 149716913 149716914 CCTCAGCTTCCCAAAGTGCAAGGATTAGAGGTATGAGCTGCTATGCTTGGCCCATAATTTTTGAT CCTCAGCTTCCCAAAGTGCAAGGATTAGAGGT_TGAGCTGCTATGCTTGGCCCATAATTTTTGAT AT A WWTR1 Ensembl:ENSG00000018408 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs745751085 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_14665456 47686 RMVar_ID_47686 Human_SNP_ID_157999658 A-to-I Human chr3 + 149836578 149836578 149836578 AAATAGTAACTGTTTGTGCATTATTTGTGGGAAAGTAAAATGGTGCAGCCACTTTGGAAAATGGT AAATAGTAACTGTTTGTGCATTATTTGTGGGAGAGTAAAATGGTGCAGCCACTTTGGAAAATGGT A G RNF13 Ensembl:ENSG00000082996 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1272140941 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_293293,RMVar_hsa_circ_19155,RMVar_hsa_circ_74239,RMVar_hsa_circ_27788,RMVar_hsa_circ_297890,RMVar_hsa_circ_222136 47687 RMVar_ID_47687 Human_SNP_ID_158017364 A-to-I Human chr3 + 149915571 149915571 149915571 ATTTGTACACCATGTTTATAGCAATATTATTTACAATAGCCAATGATGAAAGCAACCCAAGTGTA ATTTGTACACCATGTTTATAGCAATATTATTTGCAATAGCCAATGATGAAAGCAACCCAAGTGTA A G RNF13 Ensembl:ENSG00000082996 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs565104520 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19155,RMVar_hsa_circ_374011,RMVar_hsa_circ_274565,RMVar_hsa_circ_222137,RMVar_hsa_circ_222138,RMVar_hsa_circ_290588,RMVar_hsa_circ_222149,RMVar_hsa_circ_293299,RMVar_hsa_circ_222152,RMVar_hsa_circ_222155,RMVar_hsa_circ_222154,RMVar_hsa_circ_276592,RMVar_hsa_circ_289380,RMVar_hsa_circ_284614,RMVar_hsa_circ_222158 47688 RMVar_ID_47688 Human_SNP_ID_158020296 A-to-I Human chr3 + 149928745 149928745 149928745 AAAAGTTATAGAATTTTGATAGGGATTGTGCTAAATTTGTAGGTTGCTTTGGGTAGTCTTGACAT AAAAGTTATAGAATTTTGATAGGGATTGTGCTGAATTTGTAGGTTGCTTTGGGTAGTCTTGACAT A G RNF13 Ensembl:ENSG00000082996 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1439559495 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_374011,RMVar_hsa_circ_222137 47689 RMVar_ID_47689 Human_SNP_ID_158020302 A-to-I Human chr3 + 149928767 149928767 149928767 GGATTGTGCTAAATTTGTAGGTTGCTTTGGGTAGTCTTGACATCTTAACAATATTAAGTCTTCCA GGATTGTGCTAAATTTGTAGGTTGCTTTGGGTTGTCTTGACATCTTAACAATATTAAGTCTTCCA A T RNF13 Ensembl:ENSG00000082996 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1224766917 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_374011,RMVar_hsa_circ_222137 47690 RMVar_ID_47690 Human_SNP_ID_727247978 A-to-I Human chrX + 105405775 105405775 105405775 CTACTTCAACACTCAGCATTCAAGAAATATTTATCAAAGACCTGCTGTAAGCCAGGTGGTTGCTG CTACTTCAACACTCAGCATTCAAGAAATATTTGTCAAAGACCTGCTGTAAGCCAGGTGGTTGCTG A G KCTD9P2,IL1RAPL2 Ensembl:ENSG00000181819,Ensembl:ENSG00000189108 Pseudogene,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1271703541 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69277 47691 RMVar_ID_47691 Human_SNP_ID_727544515 A-to-I Human chrX + 107131998 107131998 107131998 AGAAGAAGGAAGGAGAAGAAAACATAGGTGGGATGGAATGGTTGCAAATAAAGGATAATGATTTC AGAAGAAGGAAGGAGAAGAAAACATAGGTGGGGTGGAATGGTTGCAAATAAAGGATAATGATTTC A G AL390039.1 Ensembl:ENSG00000213569 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879156619 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17443186,Human_RBP_ID_18543428 47692 RMVar_ID_47692 Human_SNP_ID_727579670 A-to-I Human chrX - 107352419 107352419 107352419 GCAAAAGAATGCAATTTGTGACAAATGTGAAGATAGAGGAGGTAAGAAAGGAGGAGTAGAGTACT GCAAAAGAATGCAATTTGTGACAAATGTGAAGGTAGAGGAGGTAAGAAAGGAGGAGTAGAGTACT T C DNAJA1P3 Ensembl:ENSG00000215007 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs765962723 Functional Loss SNV dbSNP153 33..33 33 - - - 47693 RMVar_ID_47693 Human_SNP_ID_727641561 A-to-I Human chrX - 107714629 107714629 107714629 CCCAGCTAGAGCGTGAGAACACCCTGTTGAAGACCCTGGCAAGCCCAGAGCAGCTGGAGAAGTTC CCCAGCTAGAGCGTGAGAACACCCTGTTGAAGTCCCTGGCAAGCCCAGAGCAGCTGGAGAAGTTC T A TSC22D3 Ensembl:ENSG00000157514 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs778218076 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_725110,Human_RBP_ID_1709781,Human_RBP_ID_2068506,Human_RBP_ID_5047241,Human_RBP_ID_7964294,Human_RBP_ID_8710750,Human_RBP_ID_16786889 Human_miRNA_ID_1160103 47694 RMVar_ID_47694 Human_SNP_ID_727703784 A-to-I Human chrX + 108077837 108077837 108077837 TCAAGCGATTCTCCTGCCTGAGCCTCCTGAGTAGCTGGGACTACAGGCACGTGCCACCACGCCCG TCAAGCGATTCTCCTGCCTGAGCCTCCTGAGTGGCTGGGACTACAGGCACGTGCCACCACGCCCG A G VSIG1 Ensembl:ENSG00000101842 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1417498780 Functional Loss SNV dbSNP153 33..33 33 - - - 47695 RMVar_ID_47695 Human_SNP_ID_727767449 A-to-I Human chrX + 108462436 108462436 108462436 TATTTTATTTTTGTTTGTTTCTTTTTTCAGACAGGATCTCACTCTATCACCCAGGCTGGAGTGCA TATTTTATTTTTGTTTGTTTCTTTTTTCAGACGGGATCTCACTCTATCACCCAGGCTGGAGTGCA A G COL4A5 Ensembl:ENSG00000188153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1226339570 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16787546 Human_Splice_Rec_2228587 RMVar_hsa_circ_80595,RMVar_hsa_circ_263427 47696 RMVar_ID_47696 Human_SNP_ID_727774897 A-to-I Human chrX + 108506771 108506771 108506771 CATGGCCCGGGGGTTGGGGACTCCTAAGAGATAGGTCTGACTCTGTGCCTAGGCTACACTGCACT CATGGCCCGGGGGTTGGGGACTCCTAAGAGATGGGTCTGACTCTGTGCCTAGGCTACACTGCACT A G COL4A5 Ensembl:ENSG00000188153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs774047996 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80595,RMVar_hsa_circ_263427 47697 RMVar_ID_47697 Human_SNP_ID_727800260 A-to-I Human chrX + 108648403 108648403 108648403 AGAGAAAGAAGGAGCCCTCCCTAATTCATTTTAGGAGGCCAGCATCAGCCTAATACCGAGACCAA AGAGAAAGAAGGAGCCCTCCCTAATTCATTTTGGGAGGCCAGCATCAGCCTAATACCGAGACCAA A G COL4A5 Ensembl:ENSG00000188153 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1346359340 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_31329,RMVar_hsa_circ_122959,RMVar_hsa_circ_263435,RMVar_hsa_circ_93761,RMVar_hsa_circ_263434,RMVar_hsa_circ_101541,RMVar_hsa_circ_348482,RMVar_hsa_circ_336215,RMVar_hsa_circ_91669,RMVar_hsa_circ_53142,RMVar_hsa_circ_263439,RMVar_hsa_circ_263437,RMVar_hsa_circ_263438,RMVar_hsa_circ_371440,RMVar_hsa_circ_121558,RMVar_hsa_circ_267457,RMVar_hsa_circ_263440 47698 RMVar_ID_47698 Human_SNP_ID_728022925 A-to-I Human chrX - 109724603 109724603 109724603 CTAGCCCAAAAAATACAAAAATTTAGTTGGGCATGGTGCCATGTGCCTATGGTTCCAACTACTGG CTAGCCCAAAAAATACAAAAATTTAGTTGGGCGTGGTGCCATGTGCCTATGGTTCCAACTACTGG T C ACSL4 Ensembl:ENSG00000068366 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs980509466 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17580127 RMVar_hsa_circ_90819,RMVar_hsa_circ_263458 47699 RMVar_ID_47699 Human_SNP_ID_728349486 A-to-I Human chrX - 111619853 111619853 111619853 CTCTAGCCGTGGTCCAGGAGACGGAGGGAACAAAGACCACTGGAAGGAGTCAGATAGGAAAGATG CTCTAGCCGTGGTCCAGGAGACGGAGGGAACAGAGACCACTGGAAGGAGTCAGATAGGAAAGATG T C EIF4BP7 Ensembl:ENSG00000225031 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1314244751 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5637342,Human_RBP_ID_7966221 47700 RMVar_ID_47700 Human_SNP_ID_728362736 A-to-I Human chrX + 111695268 111695268 111695268 ACCTTCTGCTGGGCGCGGGGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGTGG ACCTTCTGCTGGGCGCGGGGGCTCATGCCTGTGATCCCAGCACTTTGGGAGGCCAAGGCAGGTGG A G ALG13 Ensembl:ENSG00000101901 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs958667505 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1374,RMVar_hsa_circ_73118,RMVar_hsa_circ_11692 47701 RMVar_ID_47701 Human_SNP_ID_728362755 A-to-I Human chrX + 111695402 111695402 111695402 AAAACTAGCCCGGCTTGGTGGCACATGCCTGTAATCCCAGTCGCTCAGGAGGCTGAGGCAGGATA AAAACTAGCCCGGCTTGGTGGCACATGCCTGTGATCCCAGTCGCTCAGGAGGCTGAGGCAGGATA A G ALG13 Ensembl:ENSG00000101901 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1013535067 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26250665 RMVar_hsa_circ_1374,RMVar_hsa_circ_73118,RMVar_hsa_circ_11692 47702 RMVar_ID_47702 Human_SNP_ID_728364200 A-to-I Human chrX + 111703879 111703879 111703879 TTGGTGTTACCATTTCTCTTATGTAGTTACCTAGAAGTGGGATTGCTTGATCATATGGTAATTCT TTGGTGTTACCATTTCTCTTATGTAGTTACCTGGAAGTGGGATTGCTTGATCATATGGTAATTCT A G ALG13 Ensembl:ENSG00000101901 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031520193 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1374,RMVar_hsa_circ_73118,RMVar_hsa_circ_11692 47703 RMVar_ID_47703 Human_SNP_ID_728364270 A-to-I Human chrX + 111704425 111704425 111704425 TGCATGTGAATATTTATGGAAATATTATTCATAATAGCCCAAAAGTGGAAACAACCCAAATTTCT TGCATGTGAATATTTATGGAAATATTATTCATGATAGCCCAAAAGTGGAAACAACCCAAATTTCT A G ALG13 Ensembl:ENSG00000101901 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1281041815 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1374,RMVar_hsa_circ_73118,RMVar_hsa_circ_11692 47704 RMVar_ID_47704 Human_SNP_ID_728364277 A-to-I Human chrX + 111704465 111704465 111704465 AAAAGTGGAAACAACCCAAATTTCTATCAACTAATGAATGGATAAACAAATTTTGGTTTATGCAG AAAAGTGGAAACAACCCAAATTTCTATCAACTGATGAATGGATAAACAAATTTTGGTTTATGCAG A G ALG13 Ensembl:ENSG00000101901 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444166263 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1374,RMVar_hsa_circ_73118,RMVar_hsa_circ_11692 47705 RMVar_ID_47705 Human_SNP_ID_728364349 A-to-I Human chrX + 111705007 111705007 111705007 AGTCAATGCCTATTTCCACTCCAGCCCCGGGCAACCACTTCATCTGCTTTCTGTCTCTAGATTTA AGTCAATGCCTATTTCCACTCCAGCCCCGGGCCACCACTTCATCTGCTTTCTGTCTCTAGATTTA A C ALG13 Ensembl:ENSG00000101901 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041346234 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1374,RMVar_hsa_circ_73118,RMVar_hsa_circ_11692 47706 RMVar_ID_47706 Human_SNP_ID_728364549 A-to-I Human chrX + 111706155 111706155 111706155 CGGCTCATGCCATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCGCCCACCACCACG CGGCTCATGCCATTCTCCTGCCTCAGCCTCCCTAGTAGCTGGGACTACAGGCGCCCACCACCACG A T ALG13 Ensembl:ENSG00000101901 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1180481893 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1374,RMVar_hsa_circ_73118,RMVar_hsa_circ_11692 47707 RMVar_ID_47707 Human_SNP_ID_728364621 A-to-I Human chrX + 111706600 111706600 111706600 CAATGTGGCAAGACCCCATCTCTACAGAAAATAGAAAAATTAGCTGGGTGTGGTGGTGGCATGCA CAATGTGGCAAGACCCCATCTCTACAGAAAATGGAAAAATTAGCTGGGTGTGGTGGTGGCATGCA A G ALG13 Ensembl:ENSG00000101901 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1241665529 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1374,RMVar_hsa_circ_73118,RMVar_hsa_circ_11692 47708 RMVar_ID_47708 Human_SNP_ID_728364631 A-to-I Human chrX + 111706648 111706648 111706648 TGTGGTGGTGGCATGCACCTGTGGTCTTAGCTACTTGGGAGGCTGAGGCAGGAGGATTGTTTGAG TGTGGTGGTGGCATGCACCTGTGGTCTTAGCTGCTTGGGAGGCTGAGGCAGGAGGATTGTTTGAG A G ALG13 Ensembl:ENSG00000101901 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900871622 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16956595 RMVar_hsa_circ_1374,RMVar_hsa_circ_73118,RMVar_hsa_circ_11692 47709 RMVar_ID_47709 Human_SNP_ID_728370257 A-to-I Human chrX + 111738703 111738703 111738703 GGGACTATAGGCACACGCCACCACACTCGGCTAATTACTGTGTTTTTGTAGAGACAGGGTCTTGC GGGACTATAGGCACACGCCACCACACTCGGCTGATTACTGTGTTTTTGTAGAGACAGGGTCTTGC A G ALG13 Ensembl:ENSG00000101901 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs762772331 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2037,RMVar_hsa_circ_85668,RMVar_hsa_circ_263522,RMVar_hsa_circ_328690,RMVar_hsa_circ_35392,RMVar_hsa_circ_19650,RMVar_hsa_circ_126592,RMVar_hsa_circ_344526,RMVar_hsa_circ_263529,RMVar_hsa_circ_118355,RMVar_hsa_circ_263528 47710 RMVar_ID_47710 Human_SNP_ID_728370261 A-to-I Human chrX + 111738726 111738726 111738726 CACTCGGCTAATTACTGTGTTTTTGTAGAGACAGGGTCTTGCCATGTTGCCCAAGCTGGTCTTGA CACTCGGCTAATTACTGTGTTTTTGTAGAGACGGGGTCTTGCCATGTTGCCCAAGCTGGTCTTGA A G ALG13 Ensembl:ENSG00000101901 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs967629533 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2037,RMVar_hsa_circ_85668,RMVar_hsa_circ_263522,RMVar_hsa_circ_328690,RMVar_hsa_circ_35392,RMVar_hsa_circ_19650,RMVar_hsa_circ_126592,RMVar_hsa_circ_344526,RMVar_hsa_circ_263529,RMVar_hsa_circ_118355,RMVar_hsa_circ_263528 47711 RMVar_ID_47711 Human_SNP_ID_728370262 A-to-I Human chrX + 111738737 111738728 111738738 TTACTGTGTTTTTGTAGAGACAGGGTCTTGCCATGTTGCCCAAGCTGGTCTTGAACTCCTAGGCT TTACTGTGTTTTTGTAGAGACAGG__________GTTGCCCAAGCTGGTCTTGAACTCCTAGGCT GGTCTTGCCAT G ALG13 Ensembl:ENSG00000101901 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1380372734 Functional Loss DEL dbSNP153 25..34 33 - - - RMVar_hsa_circ_2037,RMVar_hsa_circ_85668,RMVar_hsa_circ_263522,RMVar_hsa_circ_328690,RMVar_hsa_circ_35392,RMVar_hsa_circ_19650,RMVar_hsa_circ_126592,RMVar_hsa_circ_344526,RMVar_hsa_circ_263529,RMVar_hsa_circ_118355,RMVar_hsa_circ_263528 47712 RMVar_ID_47712 Human_SNP_ID_728477464 A-to-I Human chrX + 112342890 112342890 112342890 TTGGGAGGCCAAGGCGGGCGGATCACAGGATCAGGAGTTCGAGACCAGCCTGGCCAATATGGTGA TTGGGAGGCCAAGGCGGGCGGATCACAGGATCGGGAGTTCGAGACCAGCCTGGCCAATATGGTGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1369729093 Functional Loss SNV dbSNP153 33..33 33 - - - 47713 RMVar_ID_47713 Human_SNP_ID_728907742 A-to-I Human chrX + 114776194 114776194 114776194 AAAGTGCCACCTCTCAGGTCAAAGATAAACACATTTCTTTCAGCTCCAACCTTTTTGTCTAAGCC AAAGTGCCACCTCTCAGGTCAAAGATAAACACGTTTCTTTCAGCTCCAACCTTTTTGTCTAAGCC A G HTR2C Ensembl:ENSG00000147246 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs782335152 Functional Loss SNV dbSNP153 33..33 33 - - - 47714 RMVar_ID_47714 Human_SNP_ID_728921506 A-to-I Human chrX + 114848131 114848131 114848131 CGCTGGATCGGTATGTAGCAATACGTAATCCTATTGAGCATAGCCGTTTCAATTCGCGGACTAAG CGCTGGATCGGTATGTAGCAATACGTAATCCTGTTGAGCATAGCCGTTTCAATTCGCGGACTAAG A G HTR2C Ensembl:ENSG00000147246 Protein coding CDS GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs781938388 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2230651,Human_Splice_Rec_2230671 47715 RMVar_ID_47715 Human_SNP_ID_729047186 A-to-I Human chrX - 115554816 115554816 115554816 TTTTTTTAAGACGGAGTCTCGCTCTGTTACCCAGACTGGAGTGCAATGATGCAGTCTTGGCTCAC TTTTTTTAAGACGGAGTCTCGCTCTGTTACCCGGACTGGAGTGCAATGATGCAGTCTTGGCTCAC T C PLS3-AS1 Ensembl:ENSG00000271826 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs782180070 Functional Loss SNV dbSNP153 33..33 33 - - - 47716 RMVar_ID_47716 Human_SNP_ID_729048606 A-to-I Human chrX + 115562646 115562646 115562646 GCAAGCACTTACTCCACTTTGCTGGATGTCACAATGGACTGGGGAGCCTAAACTTGATCCTCGAG GCAAGCACTTACTCCACTTTGCTGGATGTCACGATGGACTGGGGAGCCTAAACTTGATCCTCGAG A G PLS3 Ensembl:ENSG00000102024 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1231554020 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16796019 47717 RMVar_ID_47717 Human_SNP_ID_729050259 A-to-I Human chrX + 115571537 115571535 115571537 AAGACTCTGGAAAAAAAAAAAAAAGAAAAAGAAAGAGAGAAAGAGAAAAGGAAAGAGGAAAAGGA AAGACTCTGGAAAAAAAAAAAAAAGAAAAAG__AGAGAGAAAGAGAAAAGGAAAGAGGAAAAGGA GAA G PLS3 Ensembl:ENSG00000102024 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1473676537 Functional Loss DEL dbSNP153 32..33 33 - - - 47718 RMVar_ID_47718 Human_SNP_ID_729050261 A-to-I Human chrX + 115571537 115571537 115571537 AAGACTCTGGAAAAAAAAAAAAAAGAAAAAGAAAGAGAGAAAGAGAAAAGGAAAGAGGAAAAGGA AAGACTCTGGAAAAAAAAAAAAAAGAAAAAGACAGAGAGAAAGAGAAAAGGAAAGAGGAAAAGGA A C PLS3 Ensembl:ENSG00000102024 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs948312859 Functional Loss SNV dbSNP153 33..33 33 - - - 47719 RMVar_ID_47719 Human_SNP_ID_729050262 A-to-I Human chrX + 115571537 115571537 115571537 AAGACTCTGGAAAAAAAAAAAAAAGAAAAAGAAAGAGAGAAAGAGAAAAGGAAAGAGGAAAAGGA AAGACTCTGGAAAAAAAAAAAAAAGAAAAAGAGAGAGAGAAAGAGAAAAGGAAAGAGGAAAAGGA A G PLS3 Ensembl:ENSG00000102024 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs948312859 Functional Loss SNV dbSNP153 33..33 33 - - - 47720 RMVar_ID_47720 Human_SNP_ID_729051319 A-to-I Human chrX + 115577492 115577488 115577493 TTATAGGGTTTATCACTCCTGATTTTTTTTTTAATTGAGACGGAATCTTGCTCTGTTGCCCAGGC TTATAGGGTTTATCACTCCTGATTTTTTT_____TTGAGACGGAATCTTGCTCTGTTGCCCAGGC TTTTAA T PLS3 Ensembl:ENSG00000102024 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1297720869 Functional Loss DEL dbSNP153 30..34 33 - - - Human_RBP_ID_16796386 47721 RMVar_ID_47721 Human_SNP_ID_729051320 A-to-I Human chrX + 115577492 115577492 115577492 TTATAGGGTTTATCACTCCTGATTTTTTTTTTAATTGAGACGGAATCTTGCTCTGTTGCCCAGGC TTATAGGGTTTATCACTCCTGATTTTTTTTTTTATTGAGACGGAATCTTGCTCTGTTGCCCAGGC A T PLS3 Ensembl:ENSG00000102024 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs868975936 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16796386 47722 RMVar_ID_47722 Human_SNP_ID_729056490 A-to-I Human chrX + 115607097 115607097 115607097 CAAAATGGTGAAACCCCATCTCTACAAAAAATACAAAAATTAGCCAGGCATGGTGTCCCACGGCT CAAAATGGTGAAACCCCATCTCTACAAAAAATGCAAAAATTAGCCAGGCATGGTGTCCCACGGCT A G PLS3 Ensembl:ENSG00000102024 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1279507320 Functional Loss SNV dbSNP153 33..33 33 - - - 47723 RMVar_ID_47723 Human_SNP_ID_729084545 A-to-I Human chrX - 115889827 115889827 115889827 AGGTACCAGAGGCAACTGAACGCGTGAGACATAGAGCAGATGAGCTGAGAGGCAGCAAGAGAACT AGGTACCAGAGGCAACTGAACGCGTGAGACATGGAGCAGATGAGCTGAGAGGCAGCAAGAGAACT T C DANT2 Ensembl:ENSG00000235244 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1373486331 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5637350,Human_RBP_ID_16797657 47724 RMVar_ID_47724 Human_SNP_ID_729088711 A-to-I Human chrX - 115905799 115905799 115905799 ACCTGTGCTCGTTTCTGTTTTGGAACCTTCCAAGGCTCCCTCCTGTTCTTTGGGGAGTTCCCAGG ACCTGTGCTCGTTTCTGTTTTGGAACCTTCCATGGCTCCCTCCTGTTCTTTGGGGAGTTCCCAGG T A DANT2 Ensembl:ENSG00000235244 lincRNA intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs964943521 Functional Loss SNV dbSNP153 33..33 33 - - - 47725 RMVar_ID_47725 Human_SNP_ID_729088712 A-to-I Human chrX - 115905799 115905799 115905799 ACCTGTGCTCGTTTCTGTTTTGGAACCTTCCAAGGCTCCCTCCTGTTCTTTGGGGAGTTCCCAGG ACCTGTGCTCGTTTCTGTTTTGGAACCTTCCAGGGCTCCCTCCTGTTCTTTGGGGAGTTCCCAGG T C DANT2 Ensembl:ENSG00000235244 lincRNA intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs964943521 Functional Loss SNV dbSNP153 33..33 33 - - - 47726 RMVar_ID_47726 Human_SNP_ID_729093232 A-to-I Human chrX - 115925795 115925795 115925795 ATATTAGTCCTCTGTTGGATTGATAGTTTGAAAATATTTTCTCCCATATAACAGGTTGTCTCTTC ATATTAGTCCTCTGTTGGATTGATAGTTTGAATATATTTTCTCCCATATAACAGGTTGTCTCTTC T A DANT2 Ensembl:ENSG00000235244 lincRNA intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1483233432 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96302,RMVar_hsa_circ_263558 47727 RMVar_ID_47727 Human_SNP_ID_729093235 A-to-I Human chrX - 115925822 115925822 115925822 ATTGTTTGAGTTCCTTGTATATTCTGGATATTAGTCCTCTGTTGGATTGATAGTTTGAAAATATT ATTGTTTGAGTTCCTTGTATATTCTGGATATTGGTCCTCTGTTGGATTGATAGTTTGAAAATATT T C DANT2 Ensembl:ENSG00000235244 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1306126352 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96302,RMVar_hsa_circ_263558 47728 RMVar_ID_47728 Human_SNP_ID_729093268 A-to-I Human chrX - 115926022 115926022 115926022 CTCACCAACATCTGCTCTTTTTTGTCTTTTTAATAATGGCCATTCTAGCTGGGGTAAAATGAAAT CTCACCAACATCTGCTCTTTTTTGTCTTTTTAGTAATGGCCATTCTAGCTGGGGTAAAATGAAAT T C DANT2 Ensembl:ENSG00000235244 lincRNA intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1441943038 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16797922 RMVar_hsa_circ_96302,RMVar_hsa_circ_263558 47729 RMVar_ID_47729 Human_SNP_ID_729093349 A-to-I Human chrX - 115926368 115926368 115926368 AATGACCTTCAGTTTCATCTGTATGGCTGCAAAATACTTGATTGTATTCTTTTTTATGGTTGAAT AATGACCTTCAGTTTCATCTGTATGGCTGCAACATACTTGATTGTATTCTTTTTTATGGTTGAAT T G DANT2 Ensembl:ENSG00000235244 lincRNA intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1317734276 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8711454 RMVar_hsa_circ_96302,RMVar_hsa_circ_263558 47730 RMVar_ID_47730 Human_SNP_ID_729093379 A-to-I Human chrX - 115926538 115926538 115926538 AATAAATAGCTGGAGCTGTGGCATGAACCTGTAGTCCTGGCTAGTTGGAAGGCTGAGGAGGAGGG AATAAATAGCTGGAGCTGTGGCATGAACCTGTCGTCCTGGCTAGTTGGAAGGCTGAGGAGGAGGG T G DANT2 Ensembl:ENSG00000235244 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1328816224 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16797929 RMVar_hsa_circ_96302,RMVar_hsa_circ_263558 47731 RMVar_ID_47731 Human_SNP_ID_729094112 A-to-I Human chrX - 115930032 115930032 115930032 ACAAATGGACAAATGGGATCTCATCAAGTTAAAAAGCTTCTGCACAGCCAAGGAAACAAACAAAA ACAAATGGACAAATGGGATCTCATCAAGTTAAGAAGCTTCTGCACAGCCAAGGAAACAAACAAAA T C DANT2 Ensembl:ENSG00000235244 lincRNA intron GSE100210;GSE107867 HepG2 cell line;ASD brains,cerebellum - 29129909,30559470 RNA-Seq:(High) rs1366012212 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3931547 RMVar_hsa_circ_96302,RMVar_hsa_circ_263558 47732 RMVar_ID_47732 Human_SNP_ID_729094180 A-to-I Human chrX - 115930380 115930380 115930380 GCTTAATGCTGGTATAAAAACAGACACAGACCAATGGAACAGAATAGAGAATCTAGAAACATTCA GCTTAATGCTGGTATAAAAACAGACACAGACCGATGGAACAGAATAGAGAATCTAGAAACATTCA T C DANT2 Ensembl:ENSG00000235244 lincRNA intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1215289389 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3931547 RMVar_hsa_circ_96302,RMVar_hsa_circ_263558 47733 RMVar_ID_47733 Human_SNP_ID_729094197 A-to-I Human chrX - 115930483 115930483 115930483 AAGACCCAGAATAGCCAAAGCTATCCTAGGCAAAAAGAACAAACCTGGAGAATTCATATTACCTG AAGACCCAGAATAGCCAAAGCTATCCTAGGCAGAAAGAACAAACCTGGAGAATTCATATTACCTG T C DANT2 Ensembl:ENSG00000235244 lincRNA intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1386851415 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3931547 RMVar_hsa_circ_96302,RMVar_hsa_circ_263558 47734 RMVar_ID_47734 Human_SNP_ID_729094200 A-to-I Human chrX - 115930503 115930503 115930503 AAATTTCTATGTAACCACAAAAGACCCAGAATAGCCAAAGCTATCCTAGGCAAAAAGAACAAACC AAATTTCTATGTAACCACAAAAGACCCAGAATCGCCAAAGCTATCCTAGGCAAAAAGAACAAACC T G DANT2 Ensembl:ENSG00000235244 lincRNA intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1482871777 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3238324,Human_RBP_ID_3931547 RMVar_hsa_circ_96302,RMVar_hsa_circ_263558 47735 RMVar_ID_47735 Human_SNP_ID_729094239 A-to-I Human chrX - 115930710 115930710 115930710 AGCAATCAACAATCTCTGTAATGAGAATTATAAAACACTGATGAAAGAAATTGAAAAGGACACCA AGCAATCAACAATCTCTGTAATGAGAATTATAGAACACTGATGAAAGAAATTGAAAAGGACACCA T C DANT2 Ensembl:ENSG00000235244 lincRNA intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1018318481 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3238330,Human_RBP_ID_3931548,Human_RBP_ID_5107911 RMVar_hsa_circ_96302,RMVar_hsa_circ_263558 47736 RMVar_ID_47736 Human_SNP_ID_729094329 A-to-I Human chrX - 115931144 115931144 115931144 GGCATCCAAATTGGAAAGGAAGAAGTCAGATTATCCTTGTTTGCAGATGATATTATCTTTTATTT GGCATCCAAATTGGAAAGGAAGAAGTCAGATTTTCCTTGTTTGCAGATGATATTATCTTTTATTT T A DANT2 Ensembl:ENSG00000235244 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1556653841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3931549 RMVar_hsa_circ_96302,RMVar_hsa_circ_263558 47737 RMVar_ID_47737 Human_SNP_ID_729094338 A-to-I Human chrX - 115931179 115931176 115931180 TAGATAGAGCAATCAGACAAGAGAGAGAAATAAAGGGCATCCAAATTGGAAAGGAAGAAGTCAGA TAGATAGAGCAATCAGACAAGAGAGAGAAAT____GGCATCCAAATTGGAAAGGAAGAAGTCAGA CCTTT C DANT2 Ensembl:ENSG00000235244 lincRNA intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1252029552 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_3931549 RMVar_hsa_circ_96302,RMVar_hsa_circ_263558 47738 RMVar_ID_47738 Human_SNP_ID_729094338 A-to-I Human chrX - 115931180 115931176 115931180 TTAGATAGAGCAATCAGACAAGAGAGAGAAATAAAGGGCATCCAAATTGGAAAGGAAGAAGTCAG TTAGATAGAGCAATCAGACAAGAGAGAGAAAT____GGCATCCAAATTGGAAAGGAAGAAGTCAG CCTTT C DANT2 Ensembl:ENSG00000235244 lincRNA intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1252029552 Functional Loss DEL dbSNP153 33..36 33 - - - Human_RBP_ID_3931549 RMVar_hsa_circ_96302,RMVar_hsa_circ_263558 47739 RMVar_ID_47739 Human_SNP_ID_729094340 A-to-I Human chrX - 115931180 115931177 115931181 TTAGATAGAGCAATCAGACAAGAGAGAGAAATAAAGGGCATCCAAATTGGAAAGGAAGAAGTCAG TTAGATAGAGCAATCAGACAAGAGAGAGAAA____GGGCATCCAAATTGGAAAGGAAGAAGTCAG CTTTA C DANT2 Ensembl:ENSG00000235244 lincRNA intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs782568659 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_3931549 RMVar_hsa_circ_96302,RMVar_hsa_circ_263558 47740 RMVar_ID_47740 Human_SNP_ID_729095598 A-to-I Human chrX - 115937667 115937667 115937667 CCAGGCTGGCCTTGAACCCCTGAGCTCAAGCAATCCTCTCGTCTCAGCCTCCCAAAATGATAACT CCAGGCTGGCCTTGAACCCCTGAGCTCAAGCAGTCCTCTCGTCTCAGCCTCCCAAAATGATAACT T C DANT2 Ensembl:ENSG00000235244 lincRNA intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1340999524 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96302,RMVar_hsa_circ_263558 47741 RMVar_ID_47741 Human_SNP_ID_729095606 A-to-I Human chrX - 115937716 115937716 115937716 AGCTAATTATTTTTTTGCTTTTTGTAGAGACAAGGTCTCGTGATGGTTCCCAGGCTGGCCTTGAA AGCTAATTATTTTTTTGCTTTTTGTAGAGACAGGGTCTCGTGATGGTTCCCAGGCTGGCCTTGAA T C DANT2 Ensembl:ENSG00000235244 lincRNA intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs782745089 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96302,RMVar_hsa_circ_263558 47742 RMVar_ID_47742 Human_SNP_ID_729095620 A-to-I Human chrX - 115937770 115937770 115937770 TTCCTGCATCACCCTCCCAAGTAATCAGGACTAGAGGCAAGTACCACCATAGCCAGCTAATTATT TTCCTGCATCACCCTCCCAAGTAATCAGGACTGGAGGCAAGTACCACCATAGCCAGCTAATTATT T C DANT2 Ensembl:ENSG00000235244 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs955264326 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96302,RMVar_hsa_circ_263558 47743 RMVar_ID_47743 Human_SNP_ID_729095627 A-to-I Human chrX - 115937809 115937809 115937809 CAGCTCACTGCAGCCTCCAACTCCTGGGCTCAAGTGATCTTCCTGCATCACCCTCCCAAGTAATC CAGCTCACTGCAGCCTCCAACTCCTGGGCTCAGGTGATCTTCCTGCATCACCCTCCCAAGTAATC T C DANT2 Ensembl:ENSG00000235244 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1402753032 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96302,RMVar_hsa_circ_263558 47744 RMVar_ID_47744 Human_SNP_ID_729096927 A-to-I Human chrX - 115945162 115945162 115945162 GTCTTGAGCTCCTGACCGCAGGCGGTCCACCCACCTTAGCCTCCCAAGGTGCTGGGATTGCAGGC GTCTTGAGCTCCTGACCGCAGGCGGTCCACCCGCCTTAGCCTCCCAAGGTGCTGGGATTGCAGGC T C DANT2 Ensembl:ENSG00000235244 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1408205346 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96302,RMVar_hsa_circ_263558 47745 RMVar_ID_47745 Human_SNP_ID_729097137 A-to-I Human chrX - 115946175 115946175 115946175 GGAAATGCAAAAATTGGCTGGGTGTGGTGCCAAGTGCCTGTGGTCCCAGCTGCTTGAGGGGCTGA GGAAATGCAAAAATTGGCTGGGTGTGGTGCCATGTGCCTGTGGTCCCAGCTGCTTGAGGGGCTGA T A DANT2 Ensembl:ENSG00000235244 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs145737765 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96302,RMVar_hsa_circ_263558 47746 RMVar_ID_47746 Human_SNP_ID_729097138 A-to-I Human chrX - 115946175 115946175 115946175 GGAAATGCAAAAATTGGCTGGGTGTGGTGCCAAGTGCCTGTGGTCCCAGCTGCTTGAGGGGCTGA GGAAATGCAAAAATTGGCTGGGTGTGGTGCCAGGTGCCTGTGGTCCCAGCTGCTTGAGGGGCTGA T C DANT2 Ensembl:ENSG00000235244 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs145737765 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96302,RMVar_hsa_circ_263558 47747 RMVar_ID_47747 Human_SNP_ID_729506431 A-to-I Human chrX - 117937845 117937843 117937845 GGTACAGGATTTCTTTTTGCAGTGATAAAAATATTCTAAAGTTGACTCTGGATATCATTGCATAT GGTACAGGATTTCTTTTTGCAGTGATAAAAAT__TCTAAAGTTGACTCTGGATATCATTGCATAT AAT A KLHL13 Ensembl:ENSG00000003096 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1447581832 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_101831,RMVar_hsa_circ_263562,RMVar_hsa_circ_341733,RMVar_hsa_circ_71687,RMVar_hsa_circ_298752 47748 RMVar_ID_47748 Human_SNP_ID_729506433 A-to-I Human chrX - 117937849 117937849 117937849 TAAAGGTACAGGATTTCTTTTTGCAGTGATAAAAATATTCTAAAGTTGACTCTGGATATCATTGC TAAAGGTACAGGATTTCTTTTTGCAGTGATAAGAATATTCTAAAGTTGACTCTGGATATCATTGC T C KLHL13 Ensembl:ENSG00000003096 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1475799195 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3238915 RMVar_hsa_circ_101831,RMVar_hsa_circ_263562,RMVar_hsa_circ_341733,RMVar_hsa_circ_71687,RMVar_hsa_circ_298752 47749 RMVar_ID_47749 Human_SNP_ID_729532700 A-to-I Human chrX - 118081679 118081679 118081679 CAACATACAGTTAAATAGGAGGAATAAGTTCTAGTGTTTAATAGCACAATAGAGTGACTGTAGTT CAACATACAGTTAAATAGGAGGAATAAGTTCTGGTGTTTAATAGCACAATAGAGTGACTGTAGTT T C KLHL13 Ensembl:ENSG00000003096 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1345799387 Functional Loss SNV dbSNP153 33..33 33 - - - 47750 RMVar_ID_47750 Human_SNP_ID_729585375 A-to-I Human chrX + 118376982 118376982 118376982 CCATGATGGTGTCACTGCACTCAAGCCTGAGTAACGGAGTGAGACCCTATCTCAAAAAAATATGT CCATGATGGTGTCACTGCACTCAAGCCTGAGTGACGGAGTGAGACCCTATCTCAAAAAAATATGT A G WDR44 Ensembl:ENSG00000131725 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1407481356 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7968526 47751 RMVar_ID_47751 Human_SNP_ID_729591601 A-to-I Human chrX + 118413146 118413146 118413146 TCCACGTTTTTGCAATTCCAAATTGTGCTGCTATAAACGTGCGTGTGCAAGTATCTTTTTCTAAT TCCACGTTTTTGCAATTCCAAATTGTGCTGCTGTAAACGTGCGTGTGCAAGTATCTTTTTCTAAT A G WDR44 Ensembl:ENSG00000131725 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1433138602 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_367801,RMVar_hsa_circ_304112,RMVar_hsa_circ_326771,RMVar_hsa_circ_43364,RMVar_hsa_circ_15279,RMVar_hsa_circ_20503,RMVar_hsa_circ_263565,RMVar_hsa_circ_66813,RMVar_hsa_circ_355922,RMVar_hsa_circ_295084,RMVar_hsa_circ_44228,RMVar_hsa_circ_263571,RMVar_hsa_circ_263575,RMVar_hsa_circ_363806,RMVar_hsa_circ_32390,RMVar_hsa_circ_10564,RMVar_hsa_circ_358722,RMVar_hsa_circ_30940 47752 RMVar_ID_47752 Human_SNP_ID_729593502 A-to-I Human chrX + 118423971 118423971 118423971 TTTATGACTGAATAGTATTCTGTTGTGTGTATATGCCACATTTTCTTTATCCATTCATCTGTCAA TTTATGACTGAATAGTATTCTGTTGTGTGTATGTGCCACATTTTCTTTATCCATTCATCTGTCAA A G WDR44 Ensembl:ENSG00000131725 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1336699561 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_367801,RMVar_hsa_circ_304112,RMVar_hsa_circ_326771,RMVar_hsa_circ_43364,RMVar_hsa_circ_15279,RMVar_hsa_circ_20503,RMVar_hsa_circ_263565,RMVar_hsa_circ_66813,RMVar_hsa_circ_355922,RMVar_hsa_circ_295084,RMVar_hsa_circ_44228,RMVar_hsa_circ_263571,RMVar_hsa_circ_263575,RMVar_hsa_circ_363806,RMVar_hsa_circ_32390,RMVar_hsa_circ_10564,RMVar_hsa_circ_358722,RMVar_hsa_circ_30940 47753 RMVar_ID_47753 Human_SNP_ID_729593935 A-to-I Human chrX + 118425603 118425603 118425603 CTGGGAGGTGGAGGTTGCAGTGAGCCAAGATCACACCACTGCACTCCAACCTAGGTGATGGAGCA CTGGGAGGTGGAGGTTGCAGTGAGCCAAGATCTCACCACTGCACTCCAACCTAGGTGATGGAGCA A T WDR44 Ensembl:ENSG00000131725 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1471865253 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10447914 RMVar_hsa_circ_367801,RMVar_hsa_circ_304112,RMVar_hsa_circ_326771,RMVar_hsa_circ_43364,RMVar_hsa_circ_15279,RMVar_hsa_circ_20503,RMVar_hsa_circ_263565,RMVar_hsa_circ_66813,RMVar_hsa_circ_355922,RMVar_hsa_circ_295084,RMVar_hsa_circ_44228,RMVar_hsa_circ_263571,RMVar_hsa_circ_263575,RMVar_hsa_circ_363806,RMVar_hsa_circ_32390,RMVar_hsa_circ_10564,RMVar_hsa_circ_358722,RMVar_hsa_circ_30940 47754 RMVar_ID_47754 Human_SNP_ID_729594497 A-to-I Human chrX + 118428414 118428414 118428414 CTCCTGCCTCAGCCTCCCAAAGCACTGGGATTACAGGGACGAACTACCGTGCCTGGCCCTATAAA CTCCTGCCTCAGCCTCCCAAAGCACTGGGATTGCAGGGACGAACTACCGTGCCTGGCCCTATAAA A G WDR44 Ensembl:ENSG00000131725 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs764302144 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_367801,RMVar_hsa_circ_304112,RMVar_hsa_circ_326771,RMVar_hsa_circ_43364,RMVar_hsa_circ_15279,RMVar_hsa_circ_20503,RMVar_hsa_circ_263565,RMVar_hsa_circ_66813,RMVar_hsa_circ_355922,RMVar_hsa_circ_295084,RMVar_hsa_circ_44228,RMVar_hsa_circ_263571,RMVar_hsa_circ_263575,RMVar_hsa_circ_363806,RMVar_hsa_circ_32390,RMVar_hsa_circ_10564,RMVar_hsa_circ_358722,RMVar_hsa_circ_30940 47755 RMVar_ID_47755 Human_SNP_ID_729594660 A-to-I Human chrX + 118429427 118429427 118429427 CCTGGCCAACATAGTGGAACCCTGTCTCTACTAAAAATACAAAAATTAGATGGGTGTGGTGCTGT CCTGGCCAACATAGTGGAACCCTGTCTCTACTGAAAATACAAAAATTAGATGGGTGTGGTGCTGT A G WDR44 Ensembl:ENSG00000131725 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs755702538 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_367801,RMVar_hsa_circ_304112,RMVar_hsa_circ_326771,RMVar_hsa_circ_43364,RMVar_hsa_circ_15279,RMVar_hsa_circ_20503,RMVar_hsa_circ_263565,RMVar_hsa_circ_66813,RMVar_hsa_circ_355922,RMVar_hsa_circ_295084,RMVar_hsa_circ_44228,RMVar_hsa_circ_263571,RMVar_hsa_circ_263575,RMVar_hsa_circ_363806,RMVar_hsa_circ_32390,RMVar_hsa_circ_10564,RMVar_hsa_circ_358722,RMVar_hsa_circ_30940 47756 RMVar_ID_47756 Human_SNP_ID_729595044 A-to-I Human chrX + 118431524 118431524 118431524 GGAGTTTCTCCATGTTGGTCAGGCTGATCTTGAACTACCGACCTCAGGTGATCTGCCTGTCTCGG GGAGTTTCTCCATGTTGGTCAGGCTGATCTTGCACTACCGACCTCAGGTGATCTGCCTGTCTCGG A C WDR44 Ensembl:ENSG00000131725 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1176874323 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16800051 RMVar_hsa_circ_367801,RMVar_hsa_circ_304112,RMVar_hsa_circ_326771,RMVar_hsa_circ_43364,RMVar_hsa_circ_15279,RMVar_hsa_circ_20503,RMVar_hsa_circ_263565,RMVar_hsa_circ_66813,RMVar_hsa_circ_355922,RMVar_hsa_circ_295084,RMVar_hsa_circ_44228,RMVar_hsa_circ_263571,RMVar_hsa_circ_263575,RMVar_hsa_circ_363806,RMVar_hsa_circ_32390,RMVar_hsa_circ_10564,RMVar_hsa_circ_358722,RMVar_hsa_circ_30940 47757 RMVar_ID_47757 Human_SNP_ID_729596293 A-to-I Human chrX + 118438868 118438868 118438868 TGGAGTGCAGTGGCACAATCTCGGCTCACTGCAACCTCCACCTCCCGAGTTCAAGCAGTTCTGCC TGGAGTGCAGTGGCACAATCTCGGCTCACTGCTACCTCCACCTCCCGAGTTCAAGCAGTTCTGCC A T WDR44 Ensembl:ENSG00000131725 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1278980118 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_367801,RMVar_hsa_circ_304112,RMVar_hsa_circ_43364,RMVar_hsa_circ_15279,RMVar_hsa_circ_20503,RMVar_hsa_circ_263565,RMVar_hsa_circ_355922,RMVar_hsa_circ_295084,RMVar_hsa_circ_44228,RMVar_hsa_circ_263571,RMVar_hsa_circ_263575,RMVar_hsa_circ_363806,RMVar_hsa_circ_32390,RMVar_hsa_circ_10564,RMVar_hsa_circ_358722,RMVar_hsa_circ_279927,RMVar_hsa_circ_30940,RMVar_hsa_circ_343350,RMVar_hsa_circ_63215,RMVar_hsa_circ_263580,RMVar_hsa_circ_263579,RMVar_hsa_circ_319147 47758 RMVar_ID_47758 Human_SNP_ID_729597454 A-to-I Human chrX + 118445034 118445034 118445034 ATGAGAAATTTGGGCCTGGTGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGC ATGAGAAATTTGGGCCTGGTGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGC A G WDR44 Ensembl:ENSG00000131725 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1319920488 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125043,RMVar_hsa_circ_263586 47759 RMVar_ID_47759 Human_SNP_ID_729597831 A-to-I Human chrX + 118446969 118446969 118446969 ATAGCTCACTGCAACGTTGAACTCCTGTGCTCAAGCAATCTTCCTGCCTCAGCATCCCGAGTAGC ATAGCTCACTGCAACGTTGAACTCCTGTGCTCGAGCAATCTTCCTGCCTCAGCATCCCGAGTAGC A G WDR44 Ensembl:ENSG00000131725 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs921830751 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125043,RMVar_hsa_circ_263586 47760 RMVar_ID_47760 Human_SNP_ID_729616845 A-to-I Human chrX + 118549787 118549787 118549787 TGGGGTCTCCCTATGTTGTGCAGGCTGGTCTCAAACTCTTGGACTCAAGTGATCCTCCCACCTTG TGGGGTCTCCCTATGTTGTGCAGGCTGGTCTCGAACTCTTGGACTCAAGTGATCCTCCCACCTTG A G DOCK11 Ensembl:ENSG00000147251 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs755781884 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_811,RMVar_hsa_circ_106181,RMVar_hsa_circ_286061,RMVar_hsa_circ_332220,RMVar_hsa_circ_342459,RMVar_hsa_circ_268756,RMVar_hsa_circ_117763,RMVar_hsa_circ_45789,RMVar_hsa_circ_76122,RMVar_hsa_circ_3936,RMVar_hsa_circ_62626,RMVar_hsa_circ_263589,RMVar_hsa_circ_263591,RMVar_hsa_circ_263592,RMVar_hsa_circ_263593,RMVar_hsa_circ_263590,RMVar_hsa_circ_107024,RMVar_hsa_circ_263596 47761 RMVar_ID_47761 Human_SNP_ID_729700228 A-to-I Human chrX + 119018944 119018941 119018945 ATCACTTGAGGTCAGGAGTTCGAGAGCAGCCTAACTAACATGATGAAACCCTGTCTCTACTAAAA ATCACTTGAGGTCAGGAGTTCGAGAGCAGC____CTAACATGATGAAACCCTGTCTCTACTAAAA CCTAA C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1347002281 Functional Loss DEL dbSNP153 31..34 33 - - - 47762 RMVar_ID_47762 Human_SNP_ID_729741304 A-to-I Human chrX + 119243767 119243766 119243767 GTATGGATTAAGCGCTGTCCAGTAACAAAATGAAATCTCAAAACAGAGCTCAGCTGCAAAAAAGC GTATGGATTAAGCGCTGTCCAGTAACAAAATG_AATCTCAAAACAGAGCTCAGCTGCAAAAAAGC GA G PGRMC1 Ensembl:ENSG00000101856 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1175959277 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_287565,Human_RBP_ID_726336,Human_RBP_ID_1710317,Human_RBP_ID_2069277,Human_RBP_ID_7969058,Human_RBP_ID_9242490,Human_RBP_ID_16800677,Human_RBP_ID_17324606,Human_RBP_ID_17552334,Human_RBP_ID_18401804,Human_RBP_ID_26568566,Human_RBP_ID_27789537 Human_miRNA_ID_1790855 RMVar_hsa_circ_91757,RMVar_hsa_circ_263634,RMVar_hsa_circ_82971,RMVar_hsa_circ_105621,RMVar_hsa_circ_263636,RMVar_hsa_circ_263637 47763 RMVar_ID_47763 Human_SNP_ID_729771561 A-to-I Human chrX + 119416353 119416353 119416353 GCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTAGGACTGCAGGCATGTGCCACCACGCCCGGCTA GCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTGCAGGCATGTGCCACCACGCCCGGCTA A G SLC25A43 Ensembl:ENSG00000077713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1569368740 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76504,RMVar_hsa_circ_263639,RMVar_hsa_circ_299403,RMVar_hsa_circ_263643,RMVar_hsa_circ_289785,RMVar_hsa_circ_263640 47764 RMVar_ID_47764 Human_SNP_ID_729772148 A-to-I Human chrX + 119420401 119420401 119420401 CTCATTGTAGCCTCAACCTCCCGGGCCCAAGCAATCCTTCCACCTCAGCCTCCCAAGTAGCTGGG CTCATTGTAGCCTCAACCTCCCGGGCCCAAGCGATCCTTCCACCTCAGCCTCCCAAGTAGCTGGG A G SLC25A43 Ensembl:ENSG00000077713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs778246385 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76504,RMVar_hsa_circ_263639,RMVar_hsa_circ_299403,RMVar_hsa_circ_263643,RMVar_hsa_circ_289785,RMVar_hsa_circ_263640 47765 RMVar_ID_47765 Human_SNP_ID_729776132 A-to-I Human chrX + 119447342 119447342 119447342 CTCTTTTATTTTTTGAGACATGGACTCACTCTATCGCCCAGGCTGGAGTACAGTGGCACAATCAT CTCTTTTATTTTTTGAGACATGGACTCACTCTGTCGCCCAGGCTGGAGTACAGTGGCACAATCAT A G SLC25A43 Ensembl:ENSG00000077713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1197831961 Functional Loss SNV dbSNP153 33..33 33 - - - 47766 RMVar_ID_47766 Human_SNP_ID_729776590 A-to-I Human chrX + 119450392 119450392 119450392 TTATTAAATATCTACTATGTGTTAAGAATACTAAGGATACAGAAGTCAATAAAACAGATCAAAAA TTATTAAATATCTACTATGTGTTAAGAATACTGAGGATACAGAAGTCAATAAAACAGATCAAAAA A G SLC25A43 Ensembl:ENSG00000077713 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs921894709 Functional Loss SNV dbSNP153 33..33 33 - - - 47767 RMVar_ID_47767 Human_SNP_ID_729776597 A-to-I Human chrX + 119450474 119450474 119450474 GCTGAAATTCTAGTTGCAGAGAAGGAGCAGATAAATAAAGGAAATAAATAAGTAAATTATTCCAA GCTGAAATTCTAGTTGCAGAGAAGGAGCAGATGAATAAAGGAAATAAATAAGTAAATTATTCCAA A G SLC25A43 Ensembl:ENSG00000077713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1261361347 Functional Loss SNV dbSNP153 33..33 33 - - - 47768 RMVar_ID_47768 Human_SNP_ID_729777126 A-to-I Human chrX + 119453588 119453588 119453588 ACAGGGTCTTGCTCTGTCACCCAGACTGGAGTACAATGACACAATCATAGCTCACTGCAGCCTTT ACAGGGTCTTGCTCTGTCACCCAGACTGGAGTGCAATGACACAATCATAGCTCACTGCAGCCTTT A G SLC25A43 Ensembl:ENSG00000077713 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1291098875 Functional Loss SNV dbSNP153 33..33 33 - - - 47769 RMVar_ID_47769 Human_SNP_ID_729793495 A-to-I Human chrX - 119538510 119538510 119538510 AGAATTGCTTGAACTCGGGAGGTGGAGGTTGCAGTGAGCTGAGATTGCACCACTGTACTCCAGCA AGAATTGCTTGAACTCGGGAGGTGGAGGTTGCCGTGAGCTGAGATTGCACCACTGTACTCCAGCA T G CXorf56 Ensembl:ENSG00000018610 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1245568933 Functional Loss SNV dbSNP153 33..33 33 - - - 47770 RMVar_ID_47770 Human_SNP_ID_729793515 A-to-I Human chrX - 119538615 119538615 119538615 CCTGGGCAACATGGTGAAACCCTGTCTCTACTAAAATACAAAAGAAATTAGCCAGGTGTGGCGGC CCTGGGCAACATGGTGAAACCCTGTCTCTACTGAAATACAAAAGAAATTAGCCAGGTGTGGCGGC T C CXorf56 Ensembl:ENSG00000018610 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,29129909,32596459 RNA-Seq:(High) rs902768051 Functional Loss SNV dbSNP153 33..33 33 - - - 47771 RMVar_ID_47771 Human_SNP_ID_729793520 A-to-I Human chrX - 119538639 119538639 119538639 CTGAGCTCAGGAGTTTGAGACCAGCCTGGGCAACATGGTGAAACCCTGTCTCTACTAAAATACAA CTGAGCTCAGGAGTTTGAGACCAGCCTGGGCAGCATGGTGAAACCCTGTCTCTACTAAAATACAA T C CXorf56 Ensembl:ENSG00000018610 Protein coding 3'UTR GSE38233;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;esophageal squamous carcinoma cells,EC109 cell line - 24183664,32596459 RNA-Seq:(High) rs11552315 Functional Loss SNV dbSNP153 33..33 33 - - - 47772 RMVar_ID_47772 Human_SNP_ID_729793622 A-to-I Human chrX - 119539349 119539349 119539349 TTTTTGTATTTTTAGTAGAGACGGGTTCCACCATGTTGGCCAGGCTGGTCTCCAACTCCTGACCT TTTTTGTATTTTTAGTAGAGACGGGTTCCACCGTGTTGGCCAGGCTGGTCTCCAACTCCTGACCT T C CXorf56 Ensembl:ENSG00000018610 Protein coding 3'UTR GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,29796672,31158229 RNA-Seq:(High) rs1319224346 Functional Loss SNV dbSNP153 33..33 33 - - - 47773 RMVar_ID_47773 Human_SNP_ID_729793626 A-to-I Human chrX - 119539374 119539374 119539374 GGCATGTGCCACCACGCCTGGCTAATTTTTGTATTTTTAGTAGAGACGGGTTCCACCATGTTGGC GGCATGTGCCACCACGCCTGGCTAATTTTTGTGTTTTTAGTAGAGACGGGTTCCACCATGTTGGC T C CXorf56 Ensembl:ENSG00000018610 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs532020597 Functional Loss SNV dbSNP153 33..33 33 - - - 47774 RMVar_ID_47774 Human_SNP_ID_729793631 A-to-I Human chrX - 119539403 119539403 119539403 CCTCAGCCTCCTGAGTAGCTGGGATTACAGGCATGTGCCACCACGCCTGGCTAATTTTTGTATTT CCTCAGCCTCCTGAGTAGCTGGGATTACAGGCTTGTGCCACCACGCCTGGCTAATTTTTGTATTT T A CXorf56 Ensembl:ENSG00000018610 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1243552650 Functional Loss SNV dbSNP153 33..33 33 - - - 47775 RMVar_ID_47775 Human_SNP_ID_729804515 A-to-I Human chrX - 119600123 119600123 119600123 CCGCCTGCCTCGGCCTCCCAATTGCTGGGATTACAGGCATGAGCCACCACGCCTGGCCTGGTTTT CCGCCTGCCTCGGCCTCCCAATTGCTGGGATTTCAGGCATGAGCCACCACGCCTGGCCTGGTTTT T A NKRF Ensembl:ENSG00000186416 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1240815933 Functional Loss SNV dbSNP153 33..33 33 - - - 47776 RMVar_ID_47776 Human_SNP_ID_729804734 A-to-I Human chrX - 119601274 119601274 119601274 AGTGCAAGTGATTCTCCTGCCTCCACCTTCCGAGTAGCTGGGATTACAGGCGTGCACCACCACGC AGTGCAAGTGATTCTCCTGCCTCCACCTTCCGGGTAGCTGGGATTACAGGCGTGCACCACCACGC T C NKRF Ensembl:ENSG00000186416 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1357239539 Functional Loss SNV dbSNP153 33..33 33 - - - 47777 RMVar_ID_47777 Human_SNP_ID_729808860 A-to-I Human chrX - 119623633 119623633 119623633 GGTTTCACCACGTTGGCCCAGGCTGGTCTCAAACTCCTGACCTCAGGTGATCTGCCTACCTTGGC GGTTTCACCACGTTGGCCCAGGCTGGTCTCAATCTCCTGACCTCAGGTGATCTGCCTACCTTGGC T A SEPTIN6 Ensembl:ENSG00000125354 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1305571204 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99827,RMVar_hsa_circ_83687,RMVar_hsa_circ_263647,RMVar_hsa_circ_263648 47778 RMVar_ID_47778 Human_SNP_ID_729808888 A-to-I Human chrX - 119623793 119623793 119623793 ACTCTGTCACCGAGGCTGGAGTGCAGTGGCACAACCTCAGCTCCCTGCAACCTCCGCCTCCTGGG ACTCTGTCACCGAGGCTGGAGTGCAGTGGCACGACCTCAGCTCCCTGCAACCTCCGCCTCCTGGG T C SEPTIN6 Ensembl:ENSG00000125354 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1278804652 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99827,RMVar_hsa_circ_83687,RMVar_hsa_circ_263647,RMVar_hsa_circ_263648 47779 RMVar_ID_47779 Human_SNP_ID_729809133 A-to-I Human chrX - 119624770 119624770 119624770 GGGAGGCGGAGGTTGCAGTGAGCCGAGATTGCACCATTGTACTCTAGCCTGGGCAACAAGAGCGA GGGAGGCGGAGGTTGCAGTGAGCCGAGATTGCGCCATTGTACTCTAGCCTGGGCAACAAGAGCGA T C SEPTIN6 Ensembl:ENSG00000125354 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1194765478 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99827,RMVar_hsa_circ_83687,RMVar_hsa_circ_263647,RMVar_hsa_circ_263648 47780 RMVar_ID_47780 Human_SNP_ID_729809148 A-to-I Human chrX - 119624847 119624847 119624847 AAATTAGCCGGACATGGTGGCACAGGCCTGTAATCCCAGCTACTCTGGAGGCTGACACAGGAGAA AAATTAGCCGGACATGGTGGCACAGGCCTGTAGTCCCAGCTACTCTGGAGGCTGACACAGGAGAA T C SEPTIN6 Ensembl:ENSG00000125354 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs916205246 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99827,RMVar_hsa_circ_83687,RMVar_hsa_circ_263647,RMVar_hsa_circ_263648 47781 RMVar_ID_47781 Human_SNP_ID_729809157 A-to-I Human chrX - 119624905 119624905 119624905 GAAGATTGAGACCATCCTGGCTAACACGGTGAAGCTCCATCTCTACTAAAAATACAAAAAATTAG GAAGATTGAGACCATCCTGGCTAACACGGTGAGGCTCCATCTCTACTAAAAATACAAAAAATTAG T C SEPTIN6 Ensembl:ENSG00000125354 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs947634611 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99827,RMVar_hsa_circ_83687,RMVar_hsa_circ_263647,RMVar_hsa_circ_263648 47782 RMVar_ID_47782 Human_SNP_ID_729810249 A-to-I Human chrX - 119631375 119631375 119631375 GAGATCGAGACCATCCTGGCTAACTCAGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTAGC GAGATCGAGACCATCCTGGCTAACTCAGTGAATCCCCGTCTCTACTAAAAATACAAAAAATTAGC T A SEPTIN6 Ensembl:ENSG00000125354 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1013463522 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24637,RMVar_hsa_circ_99827,RMVar_hsa_circ_263648,RMVar_hsa_circ_65118,RMVar_hsa_circ_339107,RMVar_hsa_circ_278976,RMVar_hsa_circ_263650,RMVar_hsa_circ_263651 47783 RMVar_ID_47783 Human_SNP_ID_729813540 A-to-I Human chrX - 119649297 119649297 119649297 CTGAGGTCGGGAGTTTGAGACCAACCTGGCCAACATGGCAAAACCCCGTCTCTACTAAAAAATAC CTGAGGTCGGGAGTTTGAGACCAACCTGGCCACCATGGCAAAACCCCGTCTCTACTAAAAAATAC T G SEPTIN6 Ensembl:ENSG00000125354 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs769517312 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33511,RMVar_hsa_circ_99827,RMVar_hsa_circ_263648,RMVar_hsa_circ_278976,RMVar_hsa_circ_263651,RMVar_hsa_circ_337931,RMVar_hsa_circ_77794,RMVar_hsa_circ_263654,RMVar_hsa_circ_263656,RMVar_hsa_circ_292085,RMVar_hsa_circ_263653,RMVar_hsa_circ_293551,RMVar_hsa_circ_289664,RMVar_hsa_circ_263655 47784 RMVar_ID_47784 Human_SNP_ID_729813923 A-to-I Human chrX - 119651584 119651584 119651584 TCACCGCAACCTCCGCCTCCTGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGA TCACCGCAACCTCCGCCTCCTGGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGA T C SEPTIN6 Ensembl:ENSG00000125354 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1275811278 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33511,RMVar_hsa_circ_99827,RMVar_hsa_circ_263648,RMVar_hsa_circ_278976,RMVar_hsa_circ_263651,RMVar_hsa_circ_337931,RMVar_hsa_circ_77794,RMVar_hsa_circ_263654,RMVar_hsa_circ_263656,RMVar_hsa_circ_292085,RMVar_hsa_circ_263653,RMVar_hsa_circ_293551,RMVar_hsa_circ_289664,RMVar_hsa_circ_263655,RMVar_hsa_circ_263658,RMVar_hsa_circ_300990,RMVar_hsa_circ_338398,RMVar_hsa_circ_300648,RMVar_hsa_circ_263659,RMVar_hsa_circ_263657 47785 RMVar_ID_47785 Human_SNP_ID_729813999 A-to-I Human chrX - 119652061 119652061 119652061 AAATTAACTGGGCATGGTGGTGCGCATTTATAATCCCAGCTATTGGGGAGGCTCAAGCAGGAGAA AAATTAACTGGGCATGGTGGTGCGCATTTATAGTCCCAGCTATTGGGGAGGCTCAAGCAGGAGAA T C SEPTIN6 Ensembl:ENSG00000125354 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1025601865 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33511,RMVar_hsa_circ_99827,RMVar_hsa_circ_263648,RMVar_hsa_circ_278976,RMVar_hsa_circ_263651,RMVar_hsa_circ_337931,RMVar_hsa_circ_77794,RMVar_hsa_circ_263654,RMVar_hsa_circ_263656,RMVar_hsa_circ_292085,RMVar_hsa_circ_263653,RMVar_hsa_circ_293551,RMVar_hsa_circ_289664,RMVar_hsa_circ_263655,RMVar_hsa_circ_263658,RMVar_hsa_circ_300990,RMVar_hsa_circ_338398,RMVar_hsa_circ_300648,RMVar_hsa_circ_263659,RMVar_hsa_circ_263657 47786 RMVar_ID_47786 Human_SNP_ID_729814294 A-to-I Human chrX - 119653835 119653835 119653835 CGAATCCTGAGCTCAGAAGATCCGCCCGTCTCAGCCTCCCAAAGTGCTGGGATTACGAGCCATGA CGAATCCTGAGCTCAGAAGATCCGCCCGTCTCGGCCTCCCAAAGTGCTGGGATTACGAGCCATGA T C SEPTIN6 Ensembl:ENSG00000125354 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs892450539 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33511,RMVar_hsa_circ_99827,RMVar_hsa_circ_263648,RMVar_hsa_circ_337931,RMVar_hsa_circ_77794,RMVar_hsa_circ_263654,RMVar_hsa_circ_292085,RMVar_hsa_circ_263653,RMVar_hsa_circ_293551,RMVar_hsa_circ_263655,RMVar_hsa_circ_263658,RMVar_hsa_circ_338398,RMVar_hsa_circ_300648,RMVar_hsa_circ_263659 47787 RMVar_ID_47787 Human_SNP_ID_729814311 A-to-I Human chrX - 119653921 119653921 119653921 GGGATTACAGGCATGAGCTACCACAGCTGGCTAATTTTTGTATTTTTAGTAGAGACGAAGTTTTG GGGATTACAGGCATGAGCTACCACAGCTGGCTGATTTTTGTATTTTTAGTAGAGACGAAGTTTTG T C SEPTIN6 Ensembl:ENSG00000125354 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1378449916 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33511,RMVar_hsa_circ_99827,RMVar_hsa_circ_263648,RMVar_hsa_circ_337931,RMVar_hsa_circ_77794,RMVar_hsa_circ_263654,RMVar_hsa_circ_292085,RMVar_hsa_circ_263653,RMVar_hsa_circ_293551,RMVar_hsa_circ_263655,RMVar_hsa_circ_263658,RMVar_hsa_circ_338398,RMVar_hsa_circ_300648,RMVar_hsa_circ_263659 47788 RMVar_ID_47788 Human_SNP_ID_729814315 A-to-I Human chrX - 119653947 119653947 119653947 CTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCATGAGCTACCACAGCTGGCTAATTTTT CTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTGCAGGCATGAGCTACCACAGCTGGCTAATTTTT T C SEPTIN6 Ensembl:ENSG00000125354 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs956606985 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33511,RMVar_hsa_circ_99827,RMVar_hsa_circ_263648,RMVar_hsa_circ_337931,RMVar_hsa_circ_77794,RMVar_hsa_circ_263654,RMVar_hsa_circ_292085,RMVar_hsa_circ_263653,RMVar_hsa_circ_293551,RMVar_hsa_circ_263655,RMVar_hsa_circ_263658,RMVar_hsa_circ_338398,RMVar_hsa_circ_300648,RMVar_hsa_circ_263659 47789 RMVar_ID_47789 Human_SNP_ID_729817924 A-to-I Human chrX - 119673345 119673345 119673345 CTTTGGTTTTGTTGTCGTTGTTGTTTGAGACAAAGTGTCCCTGTGTCACCCAGGCTGGAGTGCAG CTTTGGTTTTGTTGTCGTTGTTGTTTGAGACAGAGTGTCCCTGTGTCACCCAGGCTGGAGTGCAG T C SEPTIN6 Ensembl:ENSG00000125354 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1227182751 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_33511,RMVar_hsa_circ_99827,RMVar_hsa_circ_263648,RMVar_hsa_circ_337931,RMVar_hsa_circ_263654,RMVar_hsa_circ_292085,RMVar_hsa_circ_300648,RMVar_hsa_circ_263659 47790 RMVar_ID_47790 Human_SNP_ID_729841433 A-to-I Human chrX - 119787783 119787779 119787783 GCTGGACTTGGTGGCACGTGCTTGTAGTCCTAACTATTTAGCAGGCTGAAGTGGGAGGATCACTT GCTGGACTTGGTGGCACGTGCTTGTAGTCCTA____TTTAGCAGGCTGAAGTGGGAGGATCACTT ATAGT A RPL39 Ensembl:ENSG00000198918 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1569456031 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_263662,RMVar_hsa_circ_99384,RMVar_hsa_circ_107153,RMVar_hsa_circ_263663 47791 RMVar_ID_47791 Human_SNP_ID_729841438 A-to-I Human chrX - 119787816 119787815 119787816 ACCCCCGTCCATCTCTACCAAAAATATAAATTAGCTGGACTTGGTGGCACGTGCTTGTAGTCCTA ACCCCCGTCCATCTCTACCAAAAATATAAATT_GCTGGACTTGGTGGCACGTGCTTGTAGTCCTA CT C RPL39 Ensembl:ENSG00000198918 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1054045875 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_263662,RMVar_hsa_circ_99384,RMVar_hsa_circ_107153,RMVar_hsa_circ_263663 47792 RMVar_ID_47792 Human_SNP_ID_729848604 A-to-I Human chrX - 119826147 119826147 119826147 TTGGTCCTTTTCTTTTTTTGAGACAGAGTCTCACTCTGTTACCCAGGCTGGAGTGCAGTGGCACG TTGGTCCTTTTCTTTTTTTGAGACAGAGTCTCGCTCTGTTACCCAGGCTGGAGTGCAGTGGCACG T C UPF3B Ensembl:ENSG00000125351 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1430700683 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_323342,RMVar_hsa_circ_300580,RMVar_hsa_circ_358805 47793 RMVar_ID_47793 Human_SNP_ID_729848608 A-to-I Human chrX - 119826155 119826154 119826156 GTTAATCGTTGGTCCTTTTCTTTTTTTGAGACAGAGTCTCACTCTGTTACCCAGGCTGGAGTGCA GTTAATCGTTGGTCCTTTTCTTTTTTTGAGA__GAGTCTCACTCTGTTACCCAGGCTGGAGTGCA CTG C UPF3B Ensembl:ENSG00000125351 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277438497 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_323342,RMVar_hsa_circ_300580,RMVar_hsa_circ_358805 47794 RMVar_ID_47794 Human_SNP_ID_729850231 A-to-I Human chrX - 119835376 119835376 119835376 GTAAAAACAGCCCAGTGTGGTAGTGCGTGCCTATAATCCCAGTTACTAGGTACCTGAGGTGGGAG GTAAAAACAGCCCAGTGTGGTAGTGCGTGCCTGTAATCCCAGTTACTAGGTACCTGAGGTGGGAG T C UPF3B Ensembl:ENSG00000125351 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs761714573 Functional Loss SNV dbSNP153 33..33 33 - - - 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 47795 RMVar_ID_47795 Human_SNP_ID_729853043 A-to-I Human chrX - 119850141 119850141 119850141 ATGTATGTCACCATGCCTGGCTAATTTTCTTTAAATTTTTTATAGAGATGGGGTCTCACTACGTT ATGTATGTCACCATGCCTGGCTAATTTTCTTTGAATTTTTTATAGAGATGGGGTCTCACTACGTT T C UPF3B Ensembl:ENSG00000125351 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968794754 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7969836 RMVar_hsa_circ_77325,RMVar_hsa_circ_100356,RMVar_hsa_circ_109896,RMVar_hsa_circ_263666,RMVar_hsa_circ_263667,RMVar_hsa_circ_263668,RMVar_hsa_circ_363361,RMVar_hsa_circ_365099,RMVar_hsa_circ_72356,RMVar_hsa_circ_366896,RMVar_hsa_circ_33806 47796 RMVar_ID_47796 Human_SNP_ID_729857100 A-to-I Human chrX + 119872763 119872763 119872763 GCTGGTCTCGAACTTCTGACCTCGGTTGATCCACCCGCCTTGATCTCCCAAAGTGCTGGGATTAC GCTGGTCTCGAACTTCTGACCTCGGTTGATCCCCCCGCCTTGATCTCCCAAAGTGCTGGGATTAC A C NDUFA1 Ensembl:ENSG00000125356 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs898593709 Functional Loss SNV dbSNP153 33..33 33 - - - 47797 RMVar_ID_47797 Human_SNP_ID_729866620 A-to-I Human chrX - 119922543 119922543 119922543 TTGTATAGTTAGTAGAGACAAGGTTTCACCTTATTGCCCAGGCTGGTCTCAAACTCCAGACCTCA TTGTATAGTTAGTAGAGACAAGGTTTCACCTTGTTGCCCAGGCTGGTCTCAAACTCCAGACCTCA T C NKAP Ensembl:ENSG00000101882 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs919957473 Functional Loss SNV dbSNP153 33..33 33 - - - 47798 RMVar_ID_47798 Human_SNP_ID_306600528 A-to-I Human chr7 - 144822 144822 144822 TTGTATTAGAGTTATCTGTGTATCCATTTTGTATCCCCTGAAGCACGATGAGCCACTTGAGGCCA TTGTATTAGAGTTATCTGTGTATCCATTTTGTGTCCCCTGAAGCACGATGAGCCACTTGAGGCCA T C AC093627.5 Ensembl:ENSG00000242474 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs546269996 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7709182,Human_RBP_ID_24197942 47799 RMVar_ID_47799 Human_SNP_ID_306791317 A-to-I Human chr7 - 706021 706021 706021 ACGCCCGGCTCATCTGTTTTTCTTTTCGAGACAGAGTTTTACTCTTGTTGCCCAGGCTGGAGAGC ACGCCCGGCTCATCTGTTTTTCTTTTCGAGACTGAGTTTTACTCTTGTTGCCCAGGCTGGAGAGC T A PRKAR1B Ensembl:ENSG00000188191 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs534372222 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16218653 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_243193 47800 RMVar_ID_47800 Human_SNP_ID_306791318 A-to-I Human chr7 - 706021 706021 706021 ACGCCCGGCTCATCTGTTTTTCTTTTCGAGACAGAGTTTTACTCTTGTTGCCCAGGCTGGAGAGC ACGCCCGGCTCATCTGTTTTTCTTTTCGAGACGGAGTTTTACTCTTGTTGCCCAGGCTGGAGAGC T C PRKAR1B Ensembl:ENSG00000188191 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs534372222 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16218653 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_243193 47801 RMVar_ID_47801 Human_SNP_ID_306791351 A-to-I Human chr7 - 706143 706143 706143 TTTTGTATTTTTTGTGGAGACGGGATTTCGCCATGTTGCCCAGGCTGGTCTTGAACTCCTGAGCT TTTTGTATTTTTTGTGGAGACGGGATTTCGCCGTGTTGCCCAGGCTGGTCTTGAACTCCTGAGCT T C PRKAR1B Ensembl:ENSG00000188191 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs564180921 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_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_243193 47802 RMVar_ID_47802 Human_SNP_ID_306796155 A-to-I Human chr7 - 721444 721444 721444 GAGTTTCTCCGTGTTGGTCAGGCTGGTCTTGAACTCCTGACTTCAGGTGATCCACCTGCCTCAAT GAGTTTCTCCGTGTTGGTCAGGCTGGTCTTGACCTCCTGACTTCAGGTGATCCACCTGCCTCAAT T G PRKAR1B Ensembl:ENSG00000188191 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs902815450 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85211,RMVar_hsa_circ_243193 47803 RMVar_ID_47803 Human_SNP_ID_306806126 A-to-I Human chr7 + 751835 751835 751835 ACCTCAGGTGACCCGCCTGCCTTGGCCTCGCAAAGTGCTGGGATTACAGGCATGAGCCACCGTGC ACCTCAGGTGACCCGCCTGCCTTGGCCTCGCAGAGTGCTGGGATTACAGGCATGAGCCACCGTGC A G DNAAF5 Ensembl:ENSG00000164818 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1358602855 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124696,RMVar_hsa_circ_346582,RMVar_hsa_circ_78013,RMVar_hsa_circ_120275,RMVar_hsa_circ_243200,RMVar_hsa_circ_243201,RMVar_hsa_circ_243202 47804 RMVar_ID_47804 Human_SNP_ID_306810821 A-to-I Human chr7 + 765762 765762 765762 TCACGCTGTCACCCAGGCTGGAGTGCAGTGGTACGATCACAGCTCACTGTAGCCTCAAACTTCCG TCACGCTGTCACCCAGGCTGGAGTGCAGTGGTCCGATCACAGCTCACTGTAGCCTCAAACTTCCG A C DNAAF5 Ensembl:ENSG00000164818 Protein coding intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs912050589 Functional Loss SNV dbSNP153 33..33 33 - - - 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_243202,RMVar_hsa_circ_290239,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 47805 RMVar_ID_47805 Human_SNP_ID_306810835 A-to-I Human chr7 + 765800 765800 765800 ACAGCTCACTGTAGCCTCAAACTTCCGGGATCAAGTGATTTTTCTGCCTTAGCCTCCTGAGTAGA ACAGCTCACTGTAGCCTCAAACTTCCGGGATCGAGTGATTTTTCTGCCTTAGCCTCCTGAGTAGA A G DNAAF5 Ensembl:ENSG00000164818 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285617455 Functional Loss SNV dbSNP153 33..33 33 - - - 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_243202,RMVar_hsa_circ_290239,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 47806 RMVar_ID_47806 Human_SNP_ID_306810899 A-to-I Human chr7 + 766029 766029 766029 TTTTGTATTTTTTGTAGACATGGGGTCTCTTTATGTTGCCCAGGCTGACCTCAAACTCCTAGGCT TTTTGTATTTTTTGTAGACATGGGGTCTCTTTCTGTTGCCCAGGCTGACCTCAAACTCCTAGGCT A C DNAAF5 Ensembl:ENSG00000164818 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1398052481 Functional Loss SNV dbSNP153 33..33 33 - - - 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_243202,RMVar_hsa_circ_290239,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 47807 RMVar_ID_47807 Human_SNP_ID_306811111 A-to-I Human chr7 + 766762 766762 766762 GAGCTCAGAAATTGAGGCTTCAGGGAGCTGTGATTGTACCACTGCACTCCAGCCCGGACAACAGA GAGCTCAGAAATTGAGGCTTCAGGGAGCTGTGGTTGTACCACTGCACTCCAGCCCGGACAACAGA A G DNAAF5 Ensembl:ENSG00000164818 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1310935560 Functional Loss SNV dbSNP153 33..33 33 - - - 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_243202,RMVar_hsa_circ_290239,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 47808 RMVar_ID_47808 Human_SNP_ID_306832443 A-to-I Human chr7 + 825974 825974 825974 GGACTTAAGAAACAAACCGGGCTGGGCATGGTAGCTCACACGTGTAATCCCAGAACTTTGGGAGG GGACTTAAGAAACAAACCGGGCTGGGCATGGTGGCTCACACGTGTAATCCCAGAACTTTGGGAGG A G SUN1 Ensembl:ENSG00000164828 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1056752007 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16233083 47809 RMVar_ID_47809 Human_SNP_ID_306832449 A-to-I Human chr7 + 825987 825987 825987 AAACCGGGCTGGGCATGGTAGCTCACACGTGTAATCCCAGAACTTTGGGAGGCTGAGGAAAATCG AAACCGGGCTGGGCATGGTAGCTCACACGTGTCATCCCAGAACTTTGGGAGGCTGAGGAAAATCG A C SUN1 Ensembl:ENSG00000164828 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1009528511 Functional Loss SNV dbSNP153 33..33 33 - - - 47810 RMVar_ID_47810 Human_SNP_ID_306832851 A-to-I Human chr7 + 827224 827224 827224 TTGTAGTTTTGCTAGAGACGGGGTTTCACCATATTGGCCAGGCTGGTCTCAAACTCCTAACCTCA TTGTAGTTTTGCTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTCCTAACCTCA A G SUN1 Ensembl:ENSG00000164828 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1489483969 Functional Loss SNV dbSNP153 33..33 33 - - - 47811 RMVar_ID_47811 Human_SNP_ID_306839523 A-to-I Human chr7 + 846779 846779 846779 TGTGCCTGTACTTCCAGCTACTCAGGAGGCTGAGGTGGGAGGATCGCTTGAGCTCAGGAGGCTTG TGTGCCTGTACTTCCAGCTACTCAGGAGGCTGGGGTGGGAGGATCGCTTGAGCTCAGGAGGCTTG A G SUN1 Ensembl:ENSG00000164828 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1302076516 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25889,RMVar_hsa_circ_81295,RMVar_hsa_circ_361943,RMVar_hsa_circ_243220,RMVar_hsa_circ_243221,RMVar_hsa_circ_32025,RMVar_hsa_circ_63161,RMVar_hsa_circ_9576,RMVar_hsa_circ_18165,RMVar_hsa_circ_86791,RMVar_hsa_circ_243224 47812 RMVar_ID_47812 Human_SNP_ID_306839570 A-to-I Human chr7 + 846933 846933 846933 CTACTTGGGCGGCTGAGGCAGGAGGATCACTTAGGCCCAGAGTTGAAGGCTGCAGTGAGCTATGA CTACTTGGGCGGCTGAGGCAGGAGGATCACTTCGGCCCAGAGTTGAAGGCTGCAGTGAGCTATGA A C SUN1 Ensembl:ENSG00000164828 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1286969546 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25889,RMVar_hsa_circ_81295,RMVar_hsa_circ_361943,RMVar_hsa_circ_243220,RMVar_hsa_circ_243221,RMVar_hsa_circ_32025,RMVar_hsa_circ_63161,RMVar_hsa_circ_9576,RMVar_hsa_circ_18165,RMVar_hsa_circ_86791,RMVar_hsa_circ_243224 47813 RMVar_ID_47813 Human_SNP_ID_306840949 A-to-I Human chr7 + 850390 850390 850390 CCAGATAATTTTTTTGTATTTTTAGTAGAGACAGGGTTTCACTGTGTTAGCCAGGATGGTCTCGA CCAGATAATTTTTTTGTATTTTTAGTAGAGACTGGGTTTCACTGTGTTAGCCAGGATGGTCTCGA A T SUN1 Ensembl:ENSG00000164828 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1054548157 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_175220 RMVar_hsa_circ_25889,RMVar_hsa_circ_81295,RMVar_hsa_circ_361943,RMVar_hsa_circ_243220,RMVar_hsa_circ_243221,RMVar_hsa_circ_32025,RMVar_hsa_circ_63161,RMVar_hsa_circ_9576,RMVar_hsa_circ_18165,RMVar_hsa_circ_50599,RMVar_hsa_circ_311553,RMVar_hsa_circ_304310,RMVar_hsa_circ_16055,RMVar_hsa_circ_36336,RMVar_hsa_circ_1450,RMVar_hsa_circ_243225 47814 RMVar_ID_47814 Human_SNP_ID_306847848 A-to-I Human chr7 + 870471 870471 870471 AGTTAGCCAGGCTTATGCGTGCCTGTCATCCCAGCTATTCGGGAGGCTGAGGCATGAAGATCACT AGTTAGCCAGGCTTATGCGTGCCTGTCATCCCGGCTATTCGGGAGGCTGAGGCATGAAGATCACT A G SUN1 Ensembl:ENSG00000164828 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1035009794 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32025,RMVar_hsa_circ_1450,RMVar_hsa_circ_319212,RMVar_hsa_circ_13514,RMVar_hsa_circ_243234,RMVar_hsa_circ_327903,RMVar_hsa_circ_118369,RMVar_hsa_circ_243233,RMVar_hsa_circ_118567,RMVar_hsa_circ_4341,RMVar_hsa_circ_243239,RMVar_hsa_circ_327146 47815 RMVar_ID_47815 Human_SNP_ID_306852379 A-to-I Human chr7 + 880888 880887 880889 TTCCCCAAGTTACGCTTTTTGTTTTTTGAGACAGAGTCTTGCTCTGTCGCTCAGACTGGAGAGCA TTCCCCAAGTTACGCTTTTTGTTTTTTGAGAC__AGTCTTGCTCTGTCGCTCAGACTGGAGAGCA CAG C GET4,SUN1 Ensembl:ENSG00000239857,Ensembl:ENSG00000164828 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1221242629 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_243234,RMVar_hsa_circ_118369,RMVar_hsa_circ_118567,RMVar_hsa_circ_243239 47816 RMVar_ID_47816 Human_SNP_ID_306853884 A-to-I Human chr7 + 884921 884921 884921 CTCCCACCTCAGCCTCCCGAGTAGCTGGGACCACAGGTGCACACCACCATGCCCAGCTAATTTCT CTCCCACCTCAGCCTCCCGAGTAGCTGGGACCCCAGGTGCACACCACCATGCCCAGCTAATTTCT A C GET4,SUN1 Ensembl:ENSG00000239857,Ensembl:ENSG00000164828 Protein coding,Protein coding intron,intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1222412976 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10365716 RMVar_hsa_circ_243234,RMVar_hsa_circ_118369,RMVar_hsa_circ_118567,RMVar_hsa_circ_243239 47817 RMVar_ID_47817 Human_SNP_ID_306853897 A-to-I Human chr7 + 884965 884965 884965 CACCATGCCCAGCTAATTTCTGTGTTTTTTGTAGAGACAGGGTCTCACTATGTTGCTCAGGCCAG CACCATGCCCAGCTAATTTCTGTGTTTTTTGTGGAGACAGGGTCTCACTATGTTGCTCAGGCCAG A G GET4,SUN1 Ensembl:ENSG00000239857,Ensembl:ENSG00000164828 Protein coding,Protein coding intron,intron GSE100210;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229 RNA-Seq:(High) rs1011295196 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16246359 RMVar_hsa_circ_243234,RMVar_hsa_circ_118369,RMVar_hsa_circ_118567,RMVar_hsa_circ_243239 47818 RMVar_ID_47818 Human_SNP_ID_306889552 A-to-I Human chr7 - 966355 966355 966355 GAGGCTAGGAGTTCAAGACCAGCCTGGGCAACATGGGTGAAACCCTGTCTCTACAAAACAAGAAA GAGGCTAGGAGTTCAAGACCAGCCTGGGCAACGTGGGTGAAACCCTGTCTCTACAAAACAAGAAA T C COX19 Ensembl:ENSG00000240230 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs564072371 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22366487 47819 RMVar_ID_47819 Human_SNP_ID_306892072 A-to-I Human chr7 - 974796 974796 974796 AAAATTAGTTGGGTGTGATGTGGCTCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAAATTAGTTGGGTGTGATGTGGCTCGCCTGTTGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA T A COX19 Ensembl:ENSG00000240230 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs966834098 Functional Loss SNV dbSNP153 33..33 33 - - - 47820 RMVar_ID_47820 Human_SNP_ID_306893668 A-to-I Human chr7 - 979948 979948 979948 TGGAGTTTCACGGGACGCTTTTGCAGTGTACTAGAGATCCACCAGACATCAAAAAGGAACTGTCC TGGAGTTTCACGGGACGCTTTTGCAGTGTACTGGAGATCCACCAGACATCAAAAAGGAACTGTCC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1475026993 Functional Loss SNV dbSNP153 33..33 33 - - - 47821 RMVar_ID_47821 Human_SNP_ID_306948353 A-to-I Human chr7 - 1134197 1134197 1134197 GTGATCGTGATTCACTGCACCCTTGAACTCCTAGGCTCAAGTGATTCTCCTGCCTCAACCTCCCA GTGATCGTGATTCACTGCACCCTTGAACTCCTCGGCTCAAGTGATTCTCCTGCCTCAACCTCCCA T G C7orf50 Ensembl:ENSG00000146540 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1482918084 Functional Loss SNV dbSNP153 33..33 33 - - - 47822 RMVar_ID_47822 Human_SNP_ID_306950242 A-to-I Human chr7 - 1137769 1137769 1137769 GTGTCTCGCTGTGCCACCCAGGCTGGAGTGCAATGGCGTGATCATAGCTCACTGCAGCCTCCACC GTGTCTCGCTGTGCCACCCAGGCTGGAGTGCAGTGGCGTGATCATAGCTCACTGCAGCCTCCACC T C C7orf50 Ensembl:ENSG00000146540 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs561156075 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22729904 47823 RMVar_ID_47823 Human_SNP_ID_306953064 A-to-I Human chr7 - 1148628 1148628 1148628 GTAATCCCAGCTACTCAGGAATCAGGAGAATCACTTGAACCCAGGAGGGAGAGGTTGCAGTGAGC GTAATCCCAGCTACTCAGGAATCAGGAGAATCTCTTGAACCCAGGAGGGAGAGGTTGCAGTGAGC T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs753584813 Functional Loss SNV dbSNP153 33..33 33 - - - 47824 RMVar_ID_47824 Human_SNP_ID_306953065 A-to-I Human chr7 - 1148628 1148628 1148628 GTAATCCCAGCTACTCAGGAATCAGGAGAATCACTTGAACCCAGGAGGGAGAGGTTGCAGTGAGC GTAATCCCAGCTACTCAGGAATCAGGAGAATCGCTTGAACCCAGGAGGGAGAGGTTGCAGTGAGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs753584813 Functional Loss SNV dbSNP153 33..33 33 - - - 47825 RMVar_ID_47825 Human_SNP_ID_306953079 A-to-I Human chr7 - 1148680 1148680 1148680 CCCTGTCTGTACTAAAAATACAAAAATTAGCCAGGCATGGTGGCAGGTGCCTGTAATCCCAGCTA CCCTGTCTGTACTAAAAATACAAAAATTAGCCGGGCATGGTGGCAGGTGCCTGTAATCCCAGCTA T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1285401382 Functional Loss SNV dbSNP153 33..33 33 - - - 47826 RMVar_ID_47826 Human_SNP_ID_306954281 A-to-I Human chr7 - 1151740 1151740 1151740 TTTTTTTTTTAAAAGGGATGAAGTCTTGCTCTATTGCCCAGGCTGGAGTGCAGTGGCACAATCTC TTTTTTTTTTAAAAGGGATGAAGTCTTGCTCTGTTGCCCAGGCTGGAGTGCAGTGGCACAATCTC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1044954030 Functional Loss SNV dbSNP153 33..33 33 - - - 47827 RMVar_ID_47827 Human_SNP_ID_306955089 A-to-I Human chr7 - 1153353 1153353 1153353 TGTAGTACCAGGTACTAGGCTGAAGCAGGAGAATCACTTGAGTCCAGGAGGCAGAGGTTGCAGTG TGTAGTACCAGGTACTAGGCTGAAGCAGGAGAGTCACTTGAGTCCAGGAGGCAGAGGTTGCAGTG T C ZFAND2A Ensembl:ENSG00000178381 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1298995034 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117363,RMVar_hsa_circ_243253,RMVar_hsa_circ_87040,RMVar_hsa_circ_243252 47828 RMVar_ID_47828 Human_SNP_ID_306955214 A-to-I Human chr7 - 1153723 1153723 1153723 CCAAGCTTGTCTCGAACTCCTGAGCTCAGGCAATCCACCCATCTTGGCTTCCCAAAGTGCTGGGA CCAAGCTTGTCTCGAACTCCTGAGCTCAGGCAGTCCACCCATCTTGGCTTCCCAAAGTGCTGGGA T C ZFAND2A Ensembl:ENSG00000178381 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1419684096 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17577293 RMVar_hsa_circ_117363,RMVar_hsa_circ_243253,RMVar_hsa_circ_87040,RMVar_hsa_circ_243252 47829 RMVar_ID_47829 Human_SNP_ID_306955219 A-to-I Human chr7 - 1153752 1153752 1153752 TTAGTGGAGATGGGGTTTCACCATGTTGCCCAAGCTTGTCTCGAACTCCTGAGCTCAGGCAATCC TTAGTGGAGATGGGGTTTCACCATGTTGCCCAGGCTTGTCTCGAACTCCTGAGCTCAGGCAATCC T C ZFAND2A Ensembl:ENSG00000178381 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs111984455 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117363,RMVar_hsa_circ_243253,RMVar_hsa_circ_87040,RMVar_hsa_circ_243252 47830 RMVar_ID_47830 Human_SNP_ID_306955702 A-to-I Human chr7 - 1155117 1155107 1155117 TTGTTTGTTTGTTTGTTTGTTTGTTTTGAGACAGTCTTGCTCTGTCACCCAGGCTGGAGTGCCAT TTGTTTGTTTGTTTGTTTGTTTGTTTTGAGAC__________TGTCACCCAGGCTGGAGTGCCAT AGAGCAAGACT A ZFAND2A Ensembl:ENSG00000178381 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1429437477 Functional Loss DEL dbSNP153 33..42 33 - - - RMVar_hsa_circ_117363,RMVar_hsa_circ_243253,RMVar_hsa_circ_87040,RMVar_hsa_circ_243252 47831 RMVar_ID_47831 Human_SNP_ID_306955706 A-to-I Human chr7 - 1155117 1155117 1155117 TTGTTTGTTTGTTTGTTTGTTTGTTTTGAGACAGTCTTGCTCTGTCACCCAGGCTGGAGTGCCAT TTGTTTGTTTGTTTGTTTGTTTGTTTTGAGACTGTCTTGCTCTGTCACCCAGGCTGGAGTGCCAT T A ZFAND2A Ensembl:ENSG00000178381 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1405161484 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117363,RMVar_hsa_circ_243253,RMVar_hsa_circ_87040,RMVar_hsa_circ_243252 47832 RMVar_ID_47832 Human_SNP_ID_306960706 A-to-I Human chr7 + 1168167 1168167 1168167 CAGTCAGGCGTGGTGGTGGCACCTGTAATCCCAGCTACTCGGGAGGCTGAGGCACGAGAATCACT CAGTCAGGCGTGGTGGTGGCACCTGTAATCCCGGCTACTCGGGAGGCTGAGGCACGAGAATCACT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs568021047 Functional Loss SNV dbSNP153 33..33 33 - - - 47833 RMVar_ID_47833 Human_SNP_ID_307062493 A-to-I Human chr7 - 1465192 1465192 1465192 GGTCAGGAGTTTGAGACCAGCCTGGCCAACATAGTGAAACCCCGTCTCTACTAAAAATACAAAAA GGTCAGGAGTTTGAGACCAGCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAA T C AC102953.2 Ensembl:ENSG00000273230 lincRNA exon GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1332018900 Functional Loss SNV dbSNP153 33..33 33 - - - 47834 RMVar_ID_47834 Human_SNP_ID_307224122 A-to-I Human chr7 - 1936890 1936890 1936890 ACCTGTGCTGTGTGTGTTCCTGCAGGGTGACTATGACCAGAGCAGGACCAAAGTGCTGCACATGA ACCTGTGCTGTGTGTGTTCCTGCAGGGTGACTTTGACCAGAGCAGGACCAAAGTGCTGCACATGA T A MAD1L1,AC069288.1 Ensembl:ENSG00000002822,Ensembl:ENSG00000286192 Protein coding,Protein coding CDS,3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs761979149 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22554534,Human_RBP_ID_26830100 Human_Splice_Rec_837970,Human_Splice_Rec_838002,Human_Splice_Rec_838038,Human_Splice_Rec_838074,Human_Splice_Rec_838090,Human_Splice_Rec_838096,Human_Splice_Rec_838224 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 47835 RMVar_ID_47835 Human_SNP_ID_307224123 A-to-I Human chr7 - 1936890 1936890 1936890 ACCTGTGCTGTGTGTGTTCCTGCAGGGTGACTATGACCAGAGCAGGACCAAAGTGCTGCACATGA ACCTGTGCTGTGTGTGTTCCTGCAGGGTGACTGTGACCAGAGCAGGACCAAAGTGCTGCACATGA T C MAD1L1,AC069288.1 Ensembl:ENSG00000002822,Ensembl:ENSG00000286192 Protein coding,Protein coding CDS,3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs761979149 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22554534,Human_RBP_ID_26830100 Human_Splice_Rec_837970,Human_Splice_Rec_838002,Human_Splice_Rec_838038,Human_Splice_Rec_838074,Human_Splice_Rec_838090,Human_Splice_Rec_838096,Human_Splice_Rec_838224 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 47836 RMVar_ID_47836 Human_SNP_ID_307304501 A-to-I Human chr7 - 2191684 2191684 2191684 CTTTGTGGCCCAGGCTGGAGTGTAGTGGCACAATCATGGCTTACTGCAGTCTCTGCCTCCTGGGC CTTTGTGGCCCAGGCTGGAGTGTAGTGGCACAGTCATGGCTTACTGCAGTCTCTGCCTCCTGGGC T C MAD1L1,AC069288.1 Ensembl:ENSG00000002822,Ensembl:ENSG00000286192 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1001056178 Functional Loss SNV dbSNP153 33..33 33 - - - 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 47837 RMVar_ID_47837 Human_SNP_ID_307305227 A-to-I Human chr7 - 2194084 2194084 2194084 AAAAAATTAGCCAGGCATGGTGGCACGCACCCATGGTCCCAACAACTCGAGAGGCCAAGTCAGGA AAAAAATTAGCCAGGCATGGTGGCACGCACCCGTGGTCCCAACAACTCGAGAGGCCAAGTCAGGA T C MAD1L1,AC069288.1 Ensembl:ENSG00000002822,Ensembl:ENSG00000286192 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968508405 Functional Loss SNV dbSNP153 33..33 33 - - - 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 47838 RMVar_ID_47838 Human_SNP_ID_307319627 A-to-I Human chr7 - 2238354 2238354 2238354 AGACACTGTCGTCATTGGGAAAGTTTCATCCTATTCCATGTAGTGCTTGCACCGTAGGTTCTTTA AGACACTGTCGTCATTGGGAAAGTTTCATCCTGTTCCATGTAGTGCTTGCACCGTAGGTTCTTTA T C AC069288.1,MRM2 Ensembl:ENSG00000286192,Ensembl:ENSG00000122687 Protein coding,Protein coding 3'UTR,intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs949689796 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3840860,Human_RBP_ID_16111103,Human_RBP_ID_24206912 RMVar_hsa_circ_119646,RMVar_hsa_circ_243318 47839 RMVar_ID_47839 Human_SNP_ID_307320659 A-to-I Human chr7 - 2240832 2240832 2240832 ATTAGCCGGACATGGTAGCAGGTGTGCCTGTAATCCCAGCTACTTGGGAGGCTGGGGCAGGAGAA ATTAGCCGGACATGGTAGCAGGTGTGCCTGTAGTCCCAGCTACTTGGGAGGCTGGGGCAGGAGAA T C AC069288.1,MRM2 Ensembl:ENSG00000286192,Ensembl:ENSG00000122687 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs987919046 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119646,RMVar_hsa_circ_243318 47840 RMVar_ID_47840 Human_SNP_ID_307329379 A-to-I Human chr7 - 2266030 2266030 2266030 TCATTGCAGCCTCGACCTCCTGAGTTCAAGCAATTCTCCCACTTCAGCCTCCCAGAATAGCTGGG TCATTGCAGCCTCGACCTCCTGAGTTCAAGCATTTCTCCCACTTCAGCCTCCCAGAATAGCTGGG T A SNX8 Ensembl:ENSG00000106266 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs113070491 Functional Loss SNV dbSNP153 33..33 33 - - - 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_279619,RMVar_hsa_circ_243325,RMVar_hsa_circ_56076 47841 RMVar_ID_47841 Human_SNP_ID_307329380 A-to-I Human chr7 - 2266030 2266030 2266030 TCATTGCAGCCTCGACCTCCTGAGTTCAAGCAATTCTCCCACTTCAGCCTCCCAGAATAGCTGGG TCATTGCAGCCTCGACCTCCTGAGTTCAAGCAGTTCTCCCACTTCAGCCTCCCAGAATAGCTGGG T C SNX8 Ensembl:ENSG00000106266 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs113070491 Functional Loss SNV dbSNP153 33..33 33 - - - 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_279619,RMVar_hsa_circ_243325,RMVar_hsa_circ_56076 47842 RMVar_ID_47842 Human_SNP_ID_307333913 A-to-I Human chr7 - 2278260 2278260 2278260 CCAGGCCATCGAGCCCCAGGCCATCGTGCAGCAGGTCCCAGCCCCCAGTCGAATGCAGATGCCGC CCAGGCCATCGAGCCCCAGGCCATCGTGCAGCGGGTCCCAGCCCCCAGTCGAATGCAGATGCCGC T C SNX8 Ensembl:ENSG00000106266 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1331455048 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 Human_miRNA_ID_2511443,Human_miRNA_ID_3054266 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 47843 RMVar_ID_47843 Human_SNP_ID_307338452 A-to-I Human chr7 - 2293001 2293001 2293001 ACTTATTATTTTTAGGTATAAGGTCTTACTCTATCACCCGGGCTGGAGTGCAGTGGCACGATTGT ACTTATTATTTTTAGGTATAAGGTCTTACTCTGTCACCCGGGCTGGAGTGCAGTGGCACGATTGT T C SNX8 Ensembl:ENSG00000106266 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1000328915 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118340,RMVar_hsa_circ_243327 47844 RMVar_ID_47844 Human_SNP_ID_307338496 A-to-I Human chr7 - 2293168 2293168 2293168 GGAGACCTGCGCTCATGTGATCCTCCCACCTCAGCCTCCCAAAAGTGCTATGATTACAGGCGTGA GGAGACCTGCGCTCATGTGATCCTCCCACCTCGGCCTCCCAAAAGTGCTATGATTACAGGCGTGA T C SNX8 Ensembl:ENSG00000106266 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910268492 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118340,RMVar_hsa_circ_243327 47845 RMVar_ID_47845 Human_SNP_ID_307338844 A-to-I Human chr7 - 2294224 2294224 2294224 AGTCTTGCACTTGTCGCCTGGGCTGGGGTGCAATGGCGTGATCTCGGCTCACTGCAACCTCTGCC AGTCTTGCACTTGTCGCCTGGGCTGGGGTGCAGTGGCGTGATCTCGGCTCACTGCAACCTCTGCC T C SNX8 Ensembl:ENSG00000106266 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs375915655 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118340,RMVar_hsa_circ_243327 47846 RMVar_ID_47846 Human_SNP_ID_307342721 A-to-I Human chr7 - 2305424 2305424 2305424 AGGAGGCAGAGGTTGCAGTGAGCTGAGATTGCACCACTGCACTCAAGCCTGGGCAACAGAGCAAG AGGAGGCAGAGGTTGCAGTGAGCTGAGATTGCGCCACTGCACTCAAGCCTGGGCAACAGAGCAAG T C SNX8 Ensembl:ENSG00000106266 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1208579521 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118340,RMVar_hsa_circ_243327 47847 RMVar_ID_47847 Human_SNP_ID_307345094 A-to-I Human chr7 - 2312933 2312933 2312933 AGATAGCGCCACTGCACTCCAGCCTGGGCGACAGAGCGAGACTCCGCCTCAAAAAAAACAAAACA AGATAGCGCCACTGCACTCCAGCCTGGGCGACGGAGCGAGACTCCGCCTCAAAAAAAACAAAACA T C SNX8 Ensembl:ENSG00000106266 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1029610223 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_174213 RMVar_hsa_circ_118340,RMVar_hsa_circ_243327 47848 RMVar_ID_47848 Human_SNP_ID_307349635 A-to-I Human chr7 - 2326181 2326181 2326181 TGTGTATTTTTTGTAGAGACAGGGGTCTCACTATTTTGCCCAGGCTGGTCTTGAACTCCTGAATT TGTGTATTTTTTGTAGAGACAGGGGTCTCACTGTTTTGCCCAGGCTGGTCTTGAACTCCTGAATT T C SNX8 Ensembl:ENSG00000106266 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs751360841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16118400 47849 RMVar_ID_47849 Human_SNP_ID_307349636 A-to-I Human chr7 - 2326184 2326184 2326184 ATTTGTGTATTTTTTGTAGAGACAGGGGTCTCACTATTTTGCCCAGGCTGGTCTTGAACTCCTGA ATTTGTGTATTTTTTGTAGAGACAGGGGTCTCGCTATTTTGCCCAGGCTGGTCTTGAACTCCTGA T C SNX8 Ensembl:ENSG00000106266 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1562458648 Functional Loss SNV dbSNP153 33..33 33 - - - 47850 RMVar_ID_47850 Human_SNP_ID_307350987 A-to-I Human chr7 - 2329972 2329972 2329972 ACAAAAATTAGCCGTGGTGGCATGCACCTGTAATCTCAGCTACATGGGGCGGGGGGTGGGTGGAG ACAAAAATTAGCCGTGGTGGCATGCACCTGTAGTCTCAGCTACATGGGGCGGGGGGTGGGTGGAG T C SNX8 Ensembl:ENSG00000106266 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1429914333 Functional Loss SNV dbSNP153 33..33 33 - - - 47851 RMVar_ID_47851 Human_SNP_ID_307358857 A-to-I Human chr7 - 2352668 2352668 2352668 CCACGCCTGGCTGATTTTTTTTGTATTTTTTTAGTAGAGACGAGGTTTCACCGTATTAGCCAGGA CCACGCCTGGCTGATTTTTTTTGTATTTTTTTGGTAGAGACGAGGTTTCACCGTATTAGCCAGGA T C SNX8 Ensembl:ENSG00000106266 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1288192930 Functional Loss SNV dbSNP153 33..33 33 - - - 47852 RMVar_ID_47852 Human_SNP_ID_307359129 A-to-I Human chr7 - 2353386 2353386 2353386 CATCCTATAGTTTTTTTGTTTTGTTTGTTTTCAGAGATAGGGTCTCGCTCTGTTGCCCAGGCTAG CATCCTATAGTTTTTTTGTTTTGTTTGTTTTCGGAGATAGGGTCTCGCTCTGTTGCCCAGGCTAG T C SNX8 Ensembl:ENSG00000106266 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs966673150 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17577302 47853 RMVar_ID_47853 Human_SNP_ID_307359196 A-to-I Human chr7 - 2353594 2353594 2353594 TTGATGCCACTGAACTGTATACTAAACTTCATATTAAAATGGCTAGGCCCTGCGCGGTGGCTCAC TTGATGCCACTGAACTGTATACTAAACTTCATTTTAAAATGGCTAGGCCCTGCGCGGTGGCTCAC T A SNX8 Ensembl:ENSG00000106266 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1484644439 Functional Loss SNV dbSNP153 33..33 33 - - - 47854 RMVar_ID_47854 Human_SNP_ID_307359199 A-to-I Human chr7 - 2353603 2353603 2353603 TGAATGTACTTGATGCCACTGAACTGTATACTAAACTTCATATTAAAATGGCTAGGCCCTGCGCG TGAATGTACTTGATGCCACTGAACTGTATACTGAACTTCATATTAAAATGGCTAGGCCCTGCGCG T C SNX8 Ensembl:ENSG00000106266 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1262765179 Functional Loss SNV dbSNP153 33..33 33 - - - 47855 RMVar_ID_47855 Human_SNP_ID_307387587 A-to-I Human chr7 + 2434904 2434904 2434904 GAGCCCAGGAGTTCAAGACCAGCTTGGGCAACATAGCAAGGACCTCATCTCTACAAAAAATAAAA GAGCCCAGGAGTTCAAGACCAGCTTGGGCAACGTAGCAAGGACCTCATCTCTACAAAAAATAAAA A G CHST12 Ensembl:ENSG00000136213 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1366668745 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_243357 47856 RMVar_ID_47856 Human_SNP_ID_307387616 A-to-I Human chr7 + 2435014 2435014 2435014 GAGGAGGGAGGATCACTTGAGCCCAGGAGTTCAAGATCAGTTTGGACCACATAGCGAGACCCTGT GAGGAGGGAGGATCACTTGAGCCCAGGAGTTCCAGATCAGTTTGGACCACATAGCGAGACCCTGT A C CHST12 Ensembl:ENSG00000136213 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs892930382 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_243357 47857 RMVar_ID_47857 Human_SNP_ID_307387618 A-to-I Human chr7 + 2435020 2435020 2435020 GGAGGATCACTTGAGCCCAGGAGTTCAAGATCAGTTTGGACCACATAGCGAGACCCTGTGTCTAC GGAGGATCACTTGAGCCCAGGAGTTCAAGATCGGTTTGGACCACATAGCGAGACCCTGTGTCTAC A G CHST12 Ensembl:ENSG00000136213 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs566653641 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16121397 RMVar_hsa_circ_243357 47858 RMVar_ID_47858 Human_SNP_ID_307389098 A-to-I Human chr7 + 2439972 2439972 2439972 AAACTCCTGAGCTCGAGTGCTCCTTCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGGG AAACTCCTGAGCTCGAGTGCTCCTTCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGGG A G CHST12 Ensembl:ENSG00000136213 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928325572 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85343,RMVar_hsa_circ_243359,RMVar_hsa_circ_243360 47859 RMVar_ID_47859 Human_SNP_ID_307391047 A-to-I Human chr7 + 2445515 2445515 2445515 TCTCACTGTGTCGCCCAGGCTCACTGCAACCTATGCCTCCCGGGTTCAAGTGGTTCTCATGCTTC TCTCACTGTGTCGCCCAGGCTCACTGCAACCTGTGCCTCCCGGGTTCAAGTGGTTCTCATGCTTC A G CHST12 Ensembl:ENSG00000136213 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs373353630 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_681515 47860 RMVar_ID_47860 Human_SNP_ID_307391497 A-to-I Human chr7 + 2446957 2446957 2446957 TCCAGTAAGACAGAGCCTCGAGTCATTCTGCCAAGAGGATCCAGAAACACAGACTTTTTCTGGGG TCCAGTAAGACAGAGCCTCGAGTCATTCTGCCGAGAGGATCCAGAAACACAGACTTTTTCTGGGG A G CHST12 Ensembl:ENSG00000136213 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs2906174 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5795,GWAS_ID_5796,GWAS_ID_5797,GWAS_ID_5798 47861 RMVar_ID_47861 Human_SNP_ID_307391498 A-to-I Human chr7 + 2446957 2446957 2446957 TCCAGTAAGACAGAGCCTCGAGTCATTCTGCCAAGAGGATCCAGAAACACAGACTTTTTCTGGGG TCCAGTAAGACAGAGCCTCGAGTCATTCTGCCTAGAGGATCCAGAAACACAGACTTTTTCTGGGG A T CHST12 Ensembl:ENSG00000136213 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs2906174 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5795,GWAS_ID_5796,GWAS_ID_5797,GWAS_ID_5798 47862 RMVar_ID_47862 Human_SNP_ID_307391645 A-to-I Human chr7 + 2447496 2447496 2447496 AATGAACACTTTTTTGTTGTTGTTGTTGAGACAGAGTCTTGCTCTGTCGCCCAGGCTGGAGTGCA AATGAACACTTTTTTGTTGTTGTTGTTGAGACGGAGTCTTGCTCTGTCGCCCAGGCTGGAGTGCA A G CHST12 Ensembl:ENSG00000136213 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1038437976 Functional Loss SNV dbSNP153 33..33 33 - - - 47863 RMVar_ID_47863 Human_SNP_ID_307393713 A-to-I Human chr7 + 2452907 2452907 2452907 GGGATCCTCCTGCTGCAGCCTCCTGAGTAGCTAGGACTATAGGCATGCGCTACCAGGCCTGACTT GGGATCCTCCTGCTGCAGCCTCCTGAGTAGCTGGGACTATAGGCATGCGCTACCAGGCCTGACTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1349838911 Functional Loss SNV dbSNP153 33..33 33 - - - 47864 RMVar_ID_47864 Human_SNP_ID_307422152 A-to-I Human chr7 - 2538198 2538198 2538198 CCTGAGGCTGTGCTGGCCATGCTCAGGTCCCTAGACCTGGAGGGCCTGCGGAGCACGCTGGCCGA CCTGAGGCTGTGCTGGCCATGCTCAGGTCCCTGGACCTGGAGGGCCTGCGGAGCACGCTGGCCGA T C BRAT1 Ensembl:ENSG00000106009 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1013387094 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5123395,Human_RBP_ID_22462982 47865 RMVar_ID_47865 Human_SNP_ID_307422153 A-to-I Human chr7 - 2538198 2538198 2538198 CCTGAGGCTGTGCTGGCCATGCTCAGGTCCCTAGACCTGGAGGGCCTGCGGAGCACGCTGGCCGA CCTGAGGCTGTGCTGGCCATGCTCAGGTCCCTCGACCTGGAGGGCCTGCGGAGCACGCTGGCCGA T G BRAT1 Ensembl:ENSG00000106009 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1013387094 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5123395,Human_RBP_ID_22462982 47866 RMVar_ID_47866 Human_SNP_ID_307428196 A-to-I Human chr7 - 2553071 2553071 2553071 CCCAGATCGTGCCACTGCACTCCAGCGACAGAATGGACTCTGTCTCAAAAAAATAGTGTCAGTCG CCCAGATCGTGCCACTGCACTCCAGCGACAGAGTGGACTCTGTCTCAAAAAAATAGTGTCAGTCG T C BRAT1 Ensembl:ENSG00000106009 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs368358477 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122173,RMVar_hsa_circ_243370 47867 RMVar_ID_47867 Human_SNP_ID_307431315 A-to-I Human chr7 + 2561628 2561628 2561628 TATTTTTGGTAGACACGGGGTTTCACCTTGTTAGCCAGGATGGTCTCGATCTCCTGACCTCGTGA TATTTTTGGTAGACACGGGGTTTCACCTTGTTGGCCAGGATGGTCTCGATCTCCTGACCTCGTGA A G IQCE Ensembl:ENSG00000106012 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1283022600 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90369,RMVar_hsa_circ_243373 47868 RMVar_ID_47868 Human_SNP_ID_307437425 A-to-I Human chr7 + 2578991 2578991 2578991 TGAGGCACAAGAATTGCTTGAACCTGTATGGCAGAGGTTGCGGTGAGTTGAGATCGCGCCACTGC TGAGGCACAAGAATTGCTTGAACCTGTATGGCGGAGGTTGCGGTGAGTTGAGATCGCGCCACTGC A G IQCE Ensembl:ENSG00000106012 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1023263474 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66428,RMVar_hsa_circ_107667,RMVar_hsa_circ_243375 47869 RMVar_ID_47869 Human_SNP_ID_307437814 A-to-I Human chr7 + 2579891 2579891 2579891 CTCCCACCTCAACCTCCTGAGTACCCGGGACTACAGGCACGTGCCACCACAGGCAGCTAATTTTT CTCCCACCTCAACCTCCTGAGTACCCGGGACTGCAGGCACGTGCCACCACAGGCAGCTAATTTTT A G IQCE Ensembl:ENSG00000106012 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1038783732 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_66428,RMVar_hsa_circ_107667,RMVar_hsa_circ_243375 47870 RMVar_ID_47870 Human_SNP_ID_307489534 A-to-I Human chr7 - 2722543 2722543 2722543 GTCCTGGCTGGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTGGGGAGGCTGAGGCGGATGGA GTCCTGGCTGGGCACGGTGGCTCACGCCTGTAGTCCCAGCACTTGGGGAGGCTGAGGCGGATGGA T C lnc-GNA12-1,lnc-GNA12-1:2,lnc-GNA12-1:3,lnc-GNA12-1:4 RNACentral:URS00008BFE5D,RNACentral:URS00009C340A,RNACentral:URS00009BCC8F,RNACentral:URS00008BCF30 lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1134412 Functional Loss SNV dbSNP153 33..33 33 - - - 47871 RMVar_ID_47871 Human_SNP_ID_307489628 A-to-I Human chr7 - 2722781 2722781 2722781 TTGTATAGAGATGGAGTCTCACTGTGTTGCCCAGGCTGGTGTTGAACTCTTGGCCTCAAGTGATC TTGTATAGAGATGGAGTCTCACTGTGTTGCCCTGGCTGGTGTTGAACTCTTGGCCTCAAGTGATC T A lnc-GNA12-1,lnc-GNA12-1:2,lnc-GNA12-1:3,lnc-GNA12-1:4 RNACentral:URS00008BFE5D,RNACentral:URS00009C340A,RNACentral:URS00009BCC8F,RNACentral:URS00008BCF30 lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1420084711 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3083859 47872 RMVar_ID_47872 Human_SNP_ID_307489637 A-to-I Human chr7 - 2722825 2722825 2722825 CACAGGCATGTGGCCACCACCCGCACCTGGCTAATTTTTAAATTTTGTATAGAGATGGAGTCTCA CACAGGCATGTGGCCACCACCCGCACCTGGCTCATTTTTAAATTTTGTATAGAGATGGAGTCTCA T G lnc-GNA12-1,lnc-GNA12-1:2,lnc-GNA12-1:3,lnc-GNA12-1:4 RNACentral:URS00008BFE5D,RNACentral:URS00009C340A,RNACentral:URS00009BCC8F,RNACentral:URS00008BCF30 lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1213403444 Functional Loss SNV dbSNP153 33..33 33 - - - 47873 RMVar_ID_47873 Human_SNP_ID_307489659 A-to-I Human chr7 - 2722883 2722883 2722883 CCTCAAAACTCCTGGGCTCAAGCAGTCCTCCCACCTTGGCCTTCCAAGTAGCTGGGACCACAGGC CCTCAAAACTCCTGGGCTCAAGCAGTCCTCCCCCCTTGGCCTTCCAAGTAGCTGGGACCACAGGC T G lnc-GNA12-1,lnc-GNA12-1:2,lnc-GNA12-1:3,lnc-GNA12-1:4 RNACentral:URS00008BFE5D,RNACentral:URS00009C340A,RNACentral:URS00009BCC8F,RNACentral:URS00008BCF30 lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1384587012 Functional Loss SNV dbSNP153 33..33 33 - - - 47874 RMVar_ID_47874 Human_SNP_ID_307489680 A-to-I Human chr7 - 2722953 2722953 2722953 TATTTTAAATATAGGGTCTTGCTCTGTGGCCCAGGCTGGAGTGCAGTGGTGTGATCATAGCTCAT TATTTTAAATATAGGGTCTTGCTCTGTGGCCCCGGCTGGAGTGCAGTGGTGTGATCATAGCTCAT T G lnc-GNA12-1,lnc-GNA12-1:2,lnc-GNA12-1:3,lnc-GNA12-1:4 RNACentral:URS00008BFE5D,RNACentral:URS00009C340A,RNACentral:URS00009BCC8F,RNACentral:URS00008BCF30 lincRNA,lincRNA,lincRNA,lincRNA exon,exon,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1045211153 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3083868 47875 RMVar_ID_47875 Human_SNP_ID_307491267 A-to-I Human chr7 - 2727202 2727201 2727202 TGGTGGGCGCCTGTAATCCTAGCTACTCGGAAAGCAGAGGCAGGAGAATCGCTTGAACCCGGTAG TGGTGGGCGCCTGTAATCCTAGCTACTCGGAA_GCAGAGGCAGGAGAATCGCTTGAACCCGGTAG CT C lnc-GNA12-1 RNACentral:URS00009BCC8F lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1204440898 Functional Loss DEL dbSNP153 33..33 33 - - - 47876 RMVar_ID_47876 Human_SNP_ID_307491268 A-to-I Human chr7 - 2727202 2727202 2727202 TGGTGGGCGCCTGTAATCCTAGCTACTCGGAAAGCAGAGGCAGGAGAATCGCTTGAACCCGGTAG TGGTGGGCGCCTGTAATCCTAGCTACTCGGAAGGCAGAGGCAGGAGAATCGCTTGAACCCGGTAG T C lnc-GNA12-1 RNACentral:URS00009BCC8F lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1227193726 Functional Loss SNV dbSNP153 33..33 33 - - - 47877 RMVar_ID_47877 Human_SNP_ID_307506285 A-to-I Human chr7 - 2770499 2770499 2770499 CCCCCACTTCAGCCTCCTGGGTAGCTGAGACTACAGGTGTGCACCACCACGCCTAGCTAACTCTA CCCCCACTTCAGCCTCCTGGGTAGCTGAGACTGCAGGTGTGCACCACCACGCCTAGCTAACTCTA T C GNA12 Ensembl:ENSG00000146535 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs927183105 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_243389,RMVar_hsa_circ_126234 47878 RMVar_ID_47878 Human_SNP_ID_307555121 A-to-I Human chr7 - 2922064 2922063 2922064 GGCTACCTGAGCTCTCTGCCTCCTATGAGAACAGAACCTACAAAGAGGACCCTGTTGGAGTGAAC GGCTACCTGAGCTCTCTGCCTCCTATGAGAAC_GAACCTACAAAGAGGACCCTGTTGGAGTGAAC CT C CARD11 Ensembl:ENSG00000198286 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1305008406 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_106479,RMVar_hsa_circ_243391 47879 RMVar_ID_47879 Human_SNP_ID_307555122 A-to-I Human chr7 - 2922064 2922064 2922064 GGCTACCTGAGCTCTCTGCCTCCTATGAGAACAGAACCTACAAAGAGGACCCTGTTGGAGTGAAC GGCTACCTGAGCTCTCTGCCTCCTATGAGAACGGAACCTACAAAGAGGACCCTGTTGGAGTGAAC T C CARD11 Ensembl:ENSG00000198286 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1423018599 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106479,RMVar_hsa_circ_243391 47880 RMVar_ID_47880 Human_SNP_ID_307555123 A-to-I Human chr7 - 2922072 2922072 2922072 ATAGCAATGGCTACCTGAGCTCTCTGCCTCCTATGAGAACAGAACCTACAAAGAGGACCCTGTTG ATAGCAATGGCTACCTGAGCTCTCTGCCTCCTGTGAGAACAGAACCTACAAAGAGGACCCTGTTG T C CARD11 Ensembl:ENSG00000198286 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs927356105 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106479,RMVar_hsa_circ_243391 47881 RMVar_ID_47881 Human_SNP_ID_307555130 A-to-I Human chr7 - 2922087 2922087 2922087 ACCAGGCCGGGGGCCATAGCAATGGCTACCTGAGCTCTCTGCCTCCTATGAGAACAGAACCTACA ACCAGGCCGGGGGCCATAGCAATGGCTACCTGGGCTCTCTGCCTCCTATGAGAACAGAACCTACA T C CARD11 Ensembl:ENSG00000198286 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs551460896 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106479,RMVar_hsa_circ_243391 47882 RMVar_ID_47882 Human_SNP_ID_307560085 A-to-I Human chr7 - 2936554 2936554 2936554 CTCACTGTTTCCCAGGCTGGTCTTAAACTCCTATCCTCAAGCGATCCTCCCGCCTCAGCCTCCCA CTCACTGTTTCCCAGGCTGGTCTTAAACTCCTGTCCTCAAGCGATCCTCCCGCCTCAGCCTCCCA T C CARD11 Ensembl:ENSG00000198286 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1243974389 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106479,RMVar_hsa_circ_243391,RMVar_hsa_circ_33947 47883 RMVar_ID_47883 Human_SNP_ID_307560098 A-to-I Human chr7 - 2936634 2936634 2936634 TTCAGCCTCCTGGGTAGCGGAACTAAAGGCACACACCACAATTCCTGACTAATTTTGTAATTTTT TTCAGCCTCCTGGGTAGCGGAACTAAAGGCACCCACCACAATTCCTGACTAATTTTGTAATTTTT T G CARD11 Ensembl:ENSG00000198286 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1183393899 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106479,RMVar_hsa_circ_243391,RMVar_hsa_circ_33947 47884 RMVar_ID_47884 Human_SNP_ID_308154291 A-to-I Human chr7 - 4636298 4636298 4636298 AAATTACCCGGGTGTGGTGGCGGGCACCGTTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAA AAATTACCCGGGTGTGGTGGCGGGCACCGTTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAA T C RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1011065290 Functional Loss SNV dbSNP153 33..33 33 - - - 47885 RMVar_ID_47885 Human_SNP_ID_308160576 A-to-I Human chr7 + 4654786 4654786 4654786 TTCAACAAATAAGAATAGTGAGGCAAAGGTTTAGCATTCTTCTAATGTCTCCTTCACTCTGGGGA TTCAACAAATAAGAATAGTGAGGCAAAGGTTTGGCATTCTTCTAATGTCTCCTTCACTCTGGGGA A G RF00017-4503 RNACentral:URS00009569F7 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984993068 Functional Loss SNV dbSNP153 33..33 33 - - - 47886 RMVar_ID_47886 Human_SNP_ID_308177041 A-to-I Human chr7 + 4707917 4707917 4707917 TGTTGGCCAGGCTGGTCACGAACTCCTGCCCCAAGTGATCCACCCTCCTCAGCCTCCCAAAGTGC TGTTGGCCAGGCTGGTCACGAACTCCTGCCCCGAGTGATCCACCCTCCTCAGCCTCCCAAAGTGC A G FOXK1 Ensembl:ENSG00000164916 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1173794721 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122648,RMVar_hsa_circ_243446 47887 RMVar_ID_47887 Human_SNP_ID_308186014 A-to-I Human chr7 + 4736042 4736042 4736042 TCTGTGGCGCGTGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCCCTTGAACCTG TCTGTGGCGCGTGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCCCTTGAACCTG A G FOXK1 Ensembl:ENSG00000164916 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041516409 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122648,RMVar_hsa_circ_243446 47888 RMVar_ID_47888 Human_SNP_ID_308190168 A-to-I Human chr7 + 4748738 4748738 4748738 AGACTTTTCATTTATTCACTGATTTAAGAGACAAGGTCTCACTTTGTTGCCCAGGCTGGTACTTC AGACTTTTCATTTATTCACTGATTTAAGAGACGAGGTCTCACTTTGTTGCCCAGGCTGGTACTTC A G FOXK1 Ensembl:ENSG00000164916 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041276957 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16169596 RMVar_hsa_circ_122648,RMVar_hsa_circ_365207,RMVar_hsa_circ_243446 47889 RMVar_ID_47889 Human_SNP_ID_308192389 A-to-I Human chr7 + 4755557 4755557 4755557 AGGAGGAGGATCAAGACCAGCCTGTGCAACATAGAGAGAACCTCTTTTCTACTAAAAATTAGCTG AGGAGGAGGATCAAGACCAGCCTGTGCAACATGGAGAGAACCTCTTTTCTACTAAAAATTAGCTG A G FOXK1 Ensembl:ENSG00000164916 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1398333153 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_365207,RMVar_hsa_circ_333414,RMVar_hsa_circ_46595,RMVar_hsa_circ_243448 47890 RMVar_ID_47890 Human_SNP_ID_308192619 A-to-I Human chr7 + 4756298 4756298 4756298 CACCACACCTGGCTATTTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGCCCAGGCTGG CACCACACCTGGCTATTTTTTGTATTTTTAGTGGAGATGGGGTTTCACCATGTTGCCCAGGCTGG A G FOXK1 Ensembl:ENSG00000164916 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1398879054 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_365207,RMVar_hsa_circ_333414,RMVar_hsa_circ_46595,RMVar_hsa_circ_243448 47891 RMVar_ID_47891 Human_SNP_ID_308192675 A-to-I Human chr7 + 4756517 4756517 4756517 TGTAAAGAATGGTAATGGCAGCCAGGCACAGTAGCTCATGCCTGTAATCCCAGCACTTTGGGAGG TGTAAAGAATGGTAATGGCAGCCAGGCACAGTCGCTCATGCCTGTAATCCCAGCACTTTGGGAGG A C FOXK1 Ensembl:ENSG00000164916 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs959946331 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_365207,RMVar_hsa_circ_333414,RMVar_hsa_circ_46595,RMVar_hsa_circ_243448 47892 RMVar_ID_47892 Human_SNP_ID_308192676 A-to-I Human chr7 + 4756517 4756517 4756517 TGTAAAGAATGGTAATGGCAGCCAGGCACAGTAGCTCATGCCTGTAATCCCAGCACTTTGGGAGG TGTAAAGAATGGTAATGGCAGCCAGGCACAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGG A G FOXK1 Ensembl:ENSG00000164916 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs959946331 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_365207,RMVar_hsa_circ_333414,RMVar_hsa_circ_46595,RMVar_hsa_circ_243448 47893 RMVar_ID_47893 Human_SNP_ID_308197398 A-to-I Human chr7 + 4769502 4769502 4769502 GCTCTATCGCCCAGGCTGGAGTGCAGTGGCCCAATCTCGGCTCACTGCAACCTCCGCCTCCCAGG GCTCTATCGCCCAGGCTGGAGTGCAGTGGCCCGATCTCGGCTCACTGCAACCTCCGCCTCCCAGG A G FOXK1 Ensembl:ENSG00000164916 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1430741076 Functional Loss SNV dbSNP153 33..33 33 - - - 47894 RMVar_ID_47894 Human_SNP_ID_308197444 A-to-I Human chr7 + 4769620 4769620 4769620 TGCCACCACACCCGGCTAATTTTTGTATTTCTAATAGAGATGAGAGTGTTACCATGTTGGTCAGG TGCCACCACACCCGGCTAATTTTTGTATTTCTGATAGAGATGAGAGTGTTACCATGTTGGTCAGG A G FOXK1 Ensembl:ENSG00000164916 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs961996063 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3091945,Human_RBP_ID_4943721,Human_RBP_ID_7743876,Human_RBP_ID_16170463,Human_RBP_ID_18382865,Human_RBP_ID_23197922,Human_RBP_ID_23315430,Human_RBP_ID_24218059,Human_RBP_ID_24516712,Human_RBP_ID_27358155 47895 RMVar_ID_47895 Human_SNP_ID_308197631 A-to-I Human chr7 + 4770257 4770257 4770257 AACAATGGGAATTTAAAATCAAATATTTGGCCAGGTGCGGTGGCTCATGCCCGTAATCCCAGCAC AACAATGGGAATTTAAAATCAAATATTTGGCCCGGTGCGGTGGCTCATGCCCGTAATCCCAGCAC A C FOXK1 Ensembl:ENSG00000164916 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs933165684 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7743897,Human_RBP_ID_17425745,Human_RBP_ID_17541648 47896 RMVar_ID_47896 Human_SNP_ID_308209283 A-to-I Human chr7 - 4794027 4794027 4794027 GCTGATTGGTGTGTTTACAAACCTTGAGCTAGATACAGAGTGCCAATTGGTTTATTTACAATCCC GCTGATTGGTGTGTTTACAAACCTTGAGCTAGCTACAGAGTGCCAATTGGTTTATTTACAATCCC T G RF00017-4489 RNACentral:URS00009982F9 SRP RNA intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs537332416 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_131 47897 RMVar_ID_47897 Human_SNP_ID_308245434 A-to-I Human chr7 - 4898200 4898200 4898200 AGAATCTGGTTACCCAGAACCCTGACCCCACTAGGAGGAATACAGGATCACATTTTATGGCCTCT AGAATCTGGTTACCCAGAACCCTGACCCCACTCGGAGGAATACAGGATCACATTTTATGGCCTCT T G RF00017-4567,RF00017-4489,lnc-MMD2-2 RNACentral:URS000094CDE3,RNACentral:URS00009982F9,RNACentral:URS00008B8A22 SRP RNA,SRP RNA,lincRNA intron,intron,intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1412054632 Functional Loss SNV dbSNP153 33..33 33 - - - 47898 RMVar_ID_47898 Human_SNP_ID_308273995 A-to-I Human chr7 + 4986873 4986873 4986873 GCCATCCTCCTGCCTCAGCTTCCCATGTAGCTAGGACTGCAGGTGCACGCCACCACACCTAGATG GCCATCCTCCTGCCTCAGCTTCCCATGTAGCTGGGACTGCAGGTGCACGCCACCACACCTAGATG A G RBAK-RBAKDN,RNF216P1 Ensembl:ENSG00000272968,Ensembl:ENSG00000196204 Protein coding,Pseudogene intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs975051640 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16171006 RMVar_hsa_circ_35982,RMVar_hsa_circ_243459,RMVar_hsa_circ_76434,RMVar_hsa_circ_303959,RMVar_hsa_circ_358893,RMVar_hsa_circ_14601 47899 RMVar_ID_47899 Human_SNP_ID_308275558 A-to-I Human chr7 + 4991640 4991640 4991640 GCGCCATCACGCCTGGGGGTTTCACCATGTTCAACAGGTTGGTCTCGAACTCCTGACCTCAGATG GCGCCATCACGCCTGGGGGTTTCACCATGTTCGACAGGTTGGTCTCGAACTCCTGACCTCAGATG A G RBAK-RBAKDN,RNF216P1 Ensembl:ENSG00000272968,Ensembl:ENSG00000196204 Protein coding,Pseudogene intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1398957112 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16171109 RMVar_hsa_circ_243461,RMVar_hsa_circ_378983 47900 RMVar_ID_47900 Human_SNP_ID_308276151 A-to-I Human chr7 + 4993387 4993387 4993387 AGGATGGTCTCGATCTCCTGACCTTGTGATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTAC AGGATGGTCTCGATCTCCTGACCTTGTGATCCCCCCGCCTCGGCCTCCCAAAGTGCTGGGATTAC A C RBAK-RBAKDN,RNF216P1 Ensembl:ENSG00000272968,Ensembl:ENSG00000196204 Protein coding,Pseudogene intron,intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1051156369 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_243461,RMVar_hsa_circ_378983 47901 RMVar_ID_47901 Human_SNP_ID_308276152 A-to-I Human chr7 + 4993387 4993387 4993387 AGGATGGTCTCGATCTCCTGACCTTGTGATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTAC AGGATGGTCTCGATCTCCTGACCTTGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTAC A G RBAK-RBAKDN,RNF216P1 Ensembl:ENSG00000272968,Ensembl:ENSG00000196204 Protein coding,Pseudogene intron,intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1051156369 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_243461,RMVar_hsa_circ_378983 47902 RMVar_ID_47902 Human_SNP_ID_308281067 A-to-I Human chr7 + 5009344 5009344 5009344 CTGGACTGCATCTGCATCCCATCCACCTAGGCAGGCAGATCATCTGAGGCCAGGAGTTCGAAACC CTGGACTGCATCTGCATCCCATCCACCTAGGCTGGCAGATCATCTGAGGCCAGGAGTTCGAAACC A T RBAK-RBAKDN,RNF216P1 Ensembl:ENSG00000272968,Ensembl:ENSG00000196204 Protein coding,Pseudogene intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs561778381 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8668427 47903 RMVar_ID_47903 Human_SNP_ID_308294861 A-to-I Human chr7 + 5056318 5056318 5056318 TAATTTATTTTTAGCAGAGATGAGGTCTTACTATGTTGCCCAAGCTGGTCTCGAACTCCTGAGCT TAATTTATTTTTAGCAGAGATGAGGTCTTACTGTGTTGCCCAAGCTGGTCTCGAACTCCTGAGCT A G RBAK-RBAKDN,RBAK Ensembl:ENSG00000272968,Ensembl:ENSG00000146587 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1258783383 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16173534 RMVar_hsa_circ_114178,RMVar_hsa_circ_121990,RMVar_hsa_circ_291002,RMVar_hsa_circ_375426,RMVar_hsa_circ_243462,RMVar_hsa_circ_370674,RMVar_hsa_circ_243463,RMVar_hsa_circ_243465,RMVar_hsa_circ_243466,RMVar_hsa_circ_243464 47904 RMVar_ID_47904 Human_SNP_ID_308298514 A-to-I Human chr7 + 5068668 5068668 5068668 ACCATTTTGAAAGCTGGCACTAAAAGCCAAGCATATGTATACTGTTTTACCCAAACCCAGCAAAA ACCATTTTGAAAGCTGGCACTAAAAGCCAAGCGTATGTATACTGTTTTACCCAAACCCAGCAAAA A G RBAK-RBAKDN,RBAK Ensembl:ENSG00000272968,Ensembl:ENSG00000146587 Protein coding,Protein coding intron,3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs887650901 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18383055,Human_RBP_ID_27769209 Human_miRNA_ID_2067058 RMVar_hsa_circ_114178,RMVar_hsa_circ_243463,RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 47905 RMVar_ID_47905 Human_SNP_ID_308343224 A-to-I Human chr7 + 5194695 5194695 5194695 TGGGGTTTCACTTTGTTGCCCCAACTGGTCTCAAACTCCTGGCTTCAAGTGATCCTCCCGCCTGG TGGGGTTTCACTTTGTTGCCCCAACTGGTCTCGAACTCCTGGCTTCAAGTGATCCTCCCGCCTGG A G WIPI2 Ensembl:ENSG00000157954 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1037347560 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 47906 RMVar_ID_47906 Human_SNP_ID_308343601 A-to-I Human chr7 + 5195918 5195918 5195918 AAAATTAGCCGGGTGTGATGGTGGTCACCTGTAATTCCAGCTGCTCGGGACGCTGAGGCAGGAGA AAAATTAGCCGGGTGTGATGGTGGTCACCTGTCATTCCAGCTGCTCGGGACGCTGAGGCAGGAGA A C WIPI2 Ensembl:ENSG00000157954 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1263207257 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 47907 RMVar_ID_47907 Human_SNP_ID_308343656 A-to-I Human chr7 + 5196084 5196084 5196084 ATCTTTTGCTGGGCGTGGTGGCTTACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGTGG ATCTTTTGCTGGGCGTGGTGGCTTACACCTGTGATCCCAGCACTTTGGGAGGCTGAGGCAGGTGG A G WIPI2 Ensembl:ENSG00000157954 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs533947867 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 47908 RMVar_ID_47908 Human_SNP_ID_308352883 A-to-I Human chr7 + 5224345 5224345 5224345 CTTGGGTTAAATCCCTTTCTCCATGCGTCTCTAGTGCCTTCCACGTATTTTTCTCACATTCCTTT CTTGGGTTAAATCCCTTTCTCCATGCGTCTCTGGTGCCTTCCACGTATTTTTCTCACATTCCTTT A G WIPI2 Ensembl:ENSG00000157954 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs990416225 Functional Loss SNV dbSNP153 33..33 33 - - - 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_243474 47909 RMVar_ID_47909 Human_SNP_ID_308389919 A-to-I Human chr7 - 5322494 5322494 5322494 TGAGACCAGGAGTTCGAGATCAGTTGGGCAACATAGTGGACCCTGTCTCTACAAAAAATAATTAG TGAGACCAGGAGTTCGAGATCAGTTGGGCAACGTAGTGGACCCTGTCTCTACAAAAAATAATTAG T C TNRC18 Ensembl:ENSG00000182095 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs9639977 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22483451 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 47910 RMVar_ID_47910 Human_SNP_ID_308391277 A-to-I Human chr7 - 5325865 5325862 5325865 TGGGTGTGGTGGTGTGCACCTGTAGTCCAGCTACTCAGGAGGCTGAGGTAGGAGGATAACGTGAG TGGGTGTGGTGGTGTGCACCTGTAGTCCAGCT___CAGGAGGCTGAGGTAGGAGGATAACGTGAG GAGT G TNRC18 Ensembl:ENSG00000182095 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1456326261 Functional Loss DEL dbSNP153 33..35 33 - - - 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 47911 RMVar_ID_47911 Human_SNP_ID_308391281 A-to-I Human chr7 - 5325874 5325874 5325874 AAACTTAGCTGGGTGTGGTGGTGTGCACCTGTAGTCCAGCTACTCAGGAGGCTGAGGTAGGAGGA AAACTTAGCTGGGTGTGGTGGTGTGCACCTGTGGTCCAGCTACTCAGGAGGCTGAGGTAGGAGGA T C TNRC18 Ensembl:ENSG00000182095 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1365381877 Functional Loss SNV dbSNP153 33..33 33 - - - 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 47912 RMVar_ID_47912 Human_SNP_ID_308392895 A-to-I Human chr7 - 5330370 5330370 5330370 CAATTAGCTGGGAGTGGTGGTGATCAGTGCCTATAGTCCCACCTACTCTGGAAGCTGGGGCAGGG CAATTAGCTGGGAGTGGTGGTGATCAGTGCCTGTAGTCCCACCTACTCTGGAAGCTGGGGCAGGG T C TNRC18 Ensembl:ENSG00000182095 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4236387 Functional Loss SNV dbSNP153 33..33 33 - - - 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 47913 RMVar_ID_47913 Human_SNP_ID_308393478 A-to-I Human chr7 - 5332191 5332191 5332191 CTTTAGTGATTCTTCTGCCCCAACCTCCCAAAATGCTGAGATTACAGGCATGAGCCACCATGCTT CTTTAGTGATTCTTCTGCCCCAACCTCCCAAATTGCTGAGATTACAGGCATGAGCCACCATGCTT T A TNRC18 Ensembl:ENSG00000182095 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1240190835 Functional Loss SNV dbSNP153 33..33 33 - - - 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 47914 RMVar_ID_47914 Human_SNP_ID_308393500 A-to-I Human chr7 - 5332271 5332271 5332271 ATGTCACTGCACCTGGCTAATTTATTGTTTGTAGAGAGGGGATCTCGCTATGTTGCCCAGGCTGA ATGTCACTGCACCTGGCTAATTTATTGTTTGTGGAGAGGGGATCTCGCTATGTTGCCCAGGCTGA T C TNRC18 Ensembl:ENSG00000182095 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1471984254 Functional Loss SNV dbSNP153 33..33 33 - - - 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 47915 RMVar_ID_47915 Human_SNP_ID_308397599 A-to-I Human chr7 - 5343574 5343574 5343574 AAAAATAAACAGAAAAATTAGCCAGGCACGGTAGCATGCGCCTCTGGTCCCAGCTACTTGGGAGG AAAAATAAACAGAAAAATTAGCCAGGCACGGTGGCATGCGCCTCTGGTCCCAGCTACTTGGGAGG T C TNRC18 Ensembl:ENSG00000182095 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1490425495 Functional Loss SNV dbSNP153 33..33 33 - - - 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_332209,RMVar_hsa_circ_105174,RMVar_hsa_circ_268646,RMVar_hsa_circ_243490,RMVar_hsa_circ_27010 47916 RMVar_ID_47916 Human_SNP_ID_308405405 A-to-I Human chr7 - 5363413 5363413 5363413 ATTTTTTAGTAGAGATGGGATTTCACCGTGTTAGCCAGGATGGTCTCCATCTCCTGACCTCATGA ATTTTTTAGTAGAGATGGGATTTCACCGTGTTGGCCAGGATGGTCTCCATCTCCTGACCTCATGA T C TNRC18 Ensembl:ENSG00000182095 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1037502378 Functional Loss SNV dbSNP153 33..33 33 - - - 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 47917 RMVar_ID_47917 Human_SNP_ID_308405686 A-to-I Human chr7 - 5364133 5364133 5364133 TACCATGCCCAGCTAATTTTTGAATTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGACTGG TACCATGCCCAGCTAATTTTTGAATTTTTAGTGGAGACAGGGTTTCACCATGTTGGCCAGACTGG T C TNRC18 Ensembl:ENSG00000182095 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1453625231 Functional Loss SNV dbSNP153 33..33 33 - - - 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 47918 RMVar_ID_47918 Human_SNP_ID_308405913 A-to-I Human chr7 - 5364696 5364696 5364696 GGGTTCAAGCGATTCTGGTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGTGGTCACCACCATG GGGTTCAAGCGATTCTGGTGCCTCAGCCTCCCTAGTAGCTGGGATTACAGGTGGTCACCACCATG T A TNRC18 Ensembl:ENSG00000182095 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1285638102 Functional Loss SNV dbSNP153 33..33 33 - - - 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 47919 RMVar_ID_47919 Human_SNP_ID_308405918 A-to-I Human chr7 - 5364722 5364722 5364722 ATGCCTCCCCGCAACCTCTGCCTCCTGGGTTCAAGCGATTCTGGTGCCTCAGCCTCCCAAGTAGC ATGCCTCCCCGCAACCTCTGCCTCCTGGGTTCGAGCGATTCTGGTGCCTCAGCCTCCCAAGTAGC T C TNRC18 Ensembl:ENSG00000182095 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1219170123 Functional Loss SNV dbSNP153 33..33 33 - - - 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 47920 RMVar_ID_47920 Human_SNP_ID_308406116 A-to-I Human chr7 - 5365236 5365236 5365236 GTGACGGCATGTGCCTGTGGTCCCAGCTACTCAGGAGGCTGAGGCAGGGTGATTGCTTGAGCCTG GTGACGGCATGTGCCTGTGGTCCCAGCTACTCGGGAGGCTGAGGCAGGGTGATTGCTTGAGCCTG T C TNRC18 Ensembl:ENSG00000182095 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs918072856 Functional Loss SNV dbSNP153 33..33 33 - - - 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 47921 RMVar_ID_47921 Human_SNP_ID_308406117 A-to-I Human chr7 - 5365236 5365236 5365236 GTGACGGCATGTGCCTGTGGTCCCAGCTACTCAGGAGGCTGAGGCAGGGTGATTGCTTGAGCCTG GTGACGGCATGTGCCTGTGGTCCCAGCTACTCCGGAGGCTGAGGCAGGGTGATTGCTTGAGCCTG T G TNRC18 Ensembl:ENSG00000182095 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs918072856 Functional Loss SNV dbSNP153 33..33 33 - - - 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 47922 RMVar_ID_47922 Human_SNP_ID_308406130 A-to-I Human chr7 - 5365295 5365295 5365295 CAGCCTGGGAAACATAGCAAGACCCCATCTCTACAAAAAAATACAAAAACTAGCTGGGTGTGACG CAGCCTGGGAAACATAGCAAGACCCCATCTCTGCAAAAAAATACAAAAACTAGCTGGGTGTGACG T C TNRC18 Ensembl:ENSG00000182095 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs187824810 Functional Loss SNV dbSNP153 33..33 33 - - - 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 47923 RMVar_ID_47923 Human_SNP_ID_308407563 A-to-I Human chr7 - 5369330 5369330 5369330 GTTTTTCTTTTTTTGAGCCATAGTCTCCCTCTATCACCCAGGCTGGTGTGCAGTGGTGTCATCTC GTTTTTCTTTTTTTGAGCCATAGTCTCCCTCTGTCACCCAGGCTGGTGTGCAGTGGTGTCATCTC T C TNRC18 Ensembl:ENSG00000182095 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs73055804 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3848499,Human_RBP_ID_16175291 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 47924 RMVar_ID_47924 Human_SNP_ID_308409002 A-to-I Human chr7 - 5373164 5373160 5373164 ACGCATCACTGGACTTGGCTATTTATTTATTTATTTTTGAGACGGAGTTTTGCTCTTGTTGCCCA ACGCATCACTGGACTTGGCTATTTATTTATTT____TTGAGACGGAGTTTTGCTCTTGTTGCCCA AAAAT A TNRC18 Ensembl:ENSG00000182095 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1001292283 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_268487,RMVar_hsa_circ_9980,RMVar_hsa_circ_268646,RMVar_hsa_circ_15667,RMVar_hsa_circ_18436,RMVar_hsa_circ_111587,RMVar_hsa_circ_243496,RMVar_hsa_circ_39440,RMVar_hsa_circ_306536 47925 RMVar_ID_47925 Human_SNP_ID_308409046 A-to-I Human chr7 - 5373277 5373277 5373277 TCTGTTGCCCCAGCTTGTACTGCAGTGGTACAATCACAGCTCACTGCAGCCTTGAACACCTGGAC TCTGTTGCCCCAGCTTGTACTGCAGTGGTACAGTCACAGCTCACTGCAGCCTTGAACACCTGGAC T C TNRC18 Ensembl:ENSG00000182095 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1048077844 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268487,RMVar_hsa_circ_9980,RMVar_hsa_circ_268646,RMVar_hsa_circ_15667,RMVar_hsa_circ_18436,RMVar_hsa_circ_111587,RMVar_hsa_circ_243496,RMVar_hsa_circ_39440,RMVar_hsa_circ_306536 47926 RMVar_ID_47926 Human_SNP_ID_308415907 A-to-I Human chr7 - 5389522 5389522 5389522 TGAACCCAGGAGGTGGAGGTTGCAGTGAGCCAAGGTTGCGCCACTGTACTCCAGCCTGGGTGAGG TGAACCCAGGAGGTGGAGGTTGCAGTGAGCCAGGGTTGCGCCACTGTACTCCAGCCTGGGTGAGG T C TNRC18 Ensembl:ENSG00000182095 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1178288049 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17577321 RMVar_hsa_circ_9980,RMVar_hsa_circ_348653,RMVar_hsa_circ_62735 47927 RMVar_ID_47927 Human_SNP_ID_308416129 A-to-I Human chr7 - 5390142 5390142 5390142 CCAGGATGGTTTCAAACTCCTGGCCTCAAGCAATCCTCCTACCTCGGCTTTCCAAAGTGCTGGGA CCAGGATGGTTTCAAACTCCTGGCCTCAAGCAGTCCTCCTACCTCGGCTTTCCAAAGTGCTGGGA T C TNRC18 Ensembl:ENSG00000182095 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs756821089 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17578044 RMVar_hsa_circ_9980,RMVar_hsa_circ_348653,RMVar_hsa_circ_62735 47928 RMVar_ID_47928 Human_SNP_ID_308416130 A-to-I Human chr7 - 5390142 5390142 5390142 CCAGGATGGTTTCAAACTCCTGGCCTCAAGCAATCCTCCTACCTCGGCTTTCCAAAGTGCTGGGA CCAGGATGGTTTCAAACTCCTGGCCTCAAGCACTCCTCCTACCTCGGCTTTCCAAAGTGCTGGGA T G TNRC18 Ensembl:ENSG00000182095 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs756821089 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17578044 RMVar_hsa_circ_9980,RMVar_hsa_circ_348653,RMVar_hsa_circ_62735 47929 RMVar_ID_47929 Human_SNP_ID_308416131 A-to-I Human chr7 - 5390143 5390143 5390143 CCCAGGATGGTTTCAAACTCCTGGCCTCAAGCAATCCTCCTACCTCGGCTTTCCAAAGTGCTGGG CCCAGGATGGTTTCAAACTCCTGGCCTCAAGCGATCCTCCTACCTCGGCTTTCCAAAGTGCTGGG T C TNRC18 Ensembl:ENSG00000182095 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1310214009 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17578044 RMVar_hsa_circ_9980,RMVar_hsa_circ_348653,RMVar_hsa_circ_62735 47930 RMVar_ID_47930 Human_SNP_ID_308416619 A-to-I Human chr7 - 5391404 5391404 5391404 AGGAGGCTGTGGCAGGAGGATCTCTTGAACTAAGGAGGTGGAGGTTGCAGTGAACCGAGATCCTG AGGAGGCTGTGGCAGGAGGATCTCTTGAACTACGGAGGTGGAGGTTGCAGTGAACCGAGATCCTG T G TNRC18 Ensembl:ENSG00000182095 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs563661333 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9980,RMVar_hsa_circ_348653,RMVar_hsa_circ_62735 47931 RMVar_ID_47931 Human_SNP_ID_308416899 A-to-I Human chr7 - 5392201 5392201 5392201 ACTCGGCCTCCCAAAATGCTGGGATTACAGGCATGAGCCACTGCTCCGGCTGGGAGTGCTGTTTG ACTCGGCCTCCCAAAATGCTGGGATTACAGGCGTGAGCCACTGCTCCGGCTGGGAGTGCTGTTTG T C TNRC18 Ensembl:ENSG00000182095 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017106359 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9980,RMVar_hsa_circ_348653,RMVar_hsa_circ_62735 47932 RMVar_ID_47932 Human_SNP_ID_308417129 A-to-I Human chr7 - 5392890 5392890 5392890 CTCCCACCTCAGCCTCCTGAGTAGCTGCGACTACAGGTGCACACCATCACGCCCGGTTAACTACT CTCCCACCTCAGCCTCCTGAGTAGCTGCGACTGCAGGTGCACACCATCACGCCCGGTTAACTACT T C TNRC18 Ensembl:ENSG00000182095 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1035719749 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9980,RMVar_hsa_circ_348653,RMVar_hsa_circ_62735 47933 RMVar_ID_47933 Human_SNP_ID_308417169 A-to-I Human chr7 - 5393006 5393006 5393006 GGGAGGGACTGTTAGGCCCTTTTTTTTGAGACAGGGTCTTGCTCTGTCGCCCAGACTGGAGTGCA GGGAGGGACTGTTAGGCCCTTTTTTTTGAGACGGGGTCTTGCTCTGTCGCCCAGACTGGAGTGCA T C TNRC18 Ensembl:ENSG00000182095 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs775336364 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9980,RMVar_hsa_circ_348653,RMVar_hsa_circ_62735 47934 RMVar_ID_47934 Human_SNP_ID_308446692 A-to-I Human chr7 - 5477016 5477016 5477016 GGGTGTGGTGGCGGGCGCCTGTGGTCCCAGCCACTCAGGAGGCTGAGGCAGGAGAATGGCATGAA GGGTGTGGTGGCGGGCGCCTGTGGTCCCAGCCGCTCAGGAGGCTGAGGCAGGAGAATGGCATGAA T C FBXL18 Ensembl:ENSG00000155034 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1024711180 Functional Loss SNV dbSNP153 33..33 33 - - - 47935 RMVar_ID_47935 Human_SNP_ID_308446880 A-to-I Human chr7 - 5477590 5477590 5477590 TCAAGCGATTCTCCCACATCAGCCTCCTGAGTAGCTGGGATTACAGGCACCTGCCATCATGACCG TCAAGCGATTCTCCCACATCAGCCTCCTGAGTGGCTGGGATTACAGGCACCTGCCATCATGACCG T C FBXL18 Ensembl:ENSG00000155034 Protein coding intron GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490829,GSM3490830,GSM3490831 HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,EC109 cell line - 29129909,29796672,31158229,31158229,32596459 RNA-Seq:(High) rs572945446 Functional Loss SNV dbSNP153 33..33 33 - - - 47936 RMVar_ID_47936 Human_SNP_ID_308446885 A-to-I Human chr7 - 5477615 5477615 5477615 TCACTACAACCTCCACCTCACAGGTTCAAGCGATTCTCCCACATCAGCCTCCTGAGTAGCTGGGA TCACTACAACCTCCACCTCACAGGTTCAAGCGTTTCTCCCACATCAGCCTCCTGAGTAGCTGGGA T A FBXL18 Ensembl:ENSG00000155034 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs985604418 Functional Loss SNV dbSNP153 33..33 33 - - - 47937 RMVar_ID_47937 Human_SNP_ID_308453990 A-to-I Human chr7 - 5498695 5498695 5498695 GTGGGAGCAGGCACCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATTGCTCTTTACCC GTGGGAGCAGGCACCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCTCTTTACCC T C FBXL18 Ensembl:ENSG00000155034 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs555860343 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_277673,RMVar_hsa_circ_243501 47938 RMVar_ID_47938 Human_SNP_ID_308453991 A-to-I Human chr7 - 5498695 5498695 5498695 GTGGGAGCAGGCACCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATTGCTCTTTACCC GTGGGAGCAGGCACCTGTAGTCCCAGCTACTCCGGAGGCTGAGGCAGGAGAATTGCTCTTTACCC T G FBXL18 Ensembl:ENSG00000155034 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs555860343 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_277673,RMVar_hsa_circ_243501 47939 RMVar_ID_47939 Human_SNP_ID_308455733 A-to-I Human chr7 - 5503385 5503385 5503385 TTGTACCACTGTGCTCCAGCCTGGACAACAGAATGAGACCTTGTCTCAAAAAACAGAAACAGGCT TTGTACCACTGTGCTCCAGCCTGGACAACAGAGTGAGACCTTGTCTCAAAAAACAGAAACAGGCT T C FBXL18 Ensembl:ENSG00000155034 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1049810529 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_277673,RMVar_hsa_circ_243501,RMVar_hsa_circ_351444 47940 RMVar_ID_47940 Human_SNP_ID_308455772 A-to-I Human chr7 - 5503510 5503510 5503510 ACAAAAAAAAAAAAGAGAAAAATGAGCATGGCATGGTGGCACATGTCTGTAGTTCCAGCTACTCA ACAAAAAAAAAAAAGAGAAAAATGAGCATGGCGTGGTGGCACATGTCTGTAGTTCCAGCTACTCA T C FBXL18 Ensembl:ENSG00000155034 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs570030929 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_277673,RMVar_hsa_circ_243501,RMVar_hsa_circ_351444 47941 RMVar_ID_47941 Human_SNP_ID_308455862 A-to-I Human chr7 - 5503855 5503841 5503856 TCAAGCGTTTTTCCTGCCCCAGCCTTCTGAGTAGCTGGGATTACAGGCGCCTGCCACCACATCTG TCAAGCGTTTTTCCTGCCCCAGCCTTCTGAG_______________GCGCCTGCCACCACATCTG CCTGTAATCCCAGCTA C FBXL18 Ensembl:ENSG00000155034 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1159065933 Functional Loss DEL dbSNP153 32..46 33 - - - RMVar_hsa_circ_277673,RMVar_hsa_circ_243501,RMVar_hsa_circ_351444 47942 RMVar_ID_47942 Human_SNP_ID_308457301 A-to-I Human chr7 - 5508435 5508435 5508435 CCCACTAATTTTTTTTTTTTTTTTTTTAGACAAAGTCTCGCTCTGTTGCCCAGGCTGGATGCAAT CCCACTAATTTTTTTTTTTTTTTTTTTAGACACAGTCTCGCTCTGTTGCCCAGGCTGGATGCAAT T G FBXL18 Ensembl:ENSG00000155034 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1310490494 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16178584 47943 RMVar_ID_47943 Human_SNP_ID_308463805 A-to-I Human chr7 - 5527386 5527386 5527386 CAGTCCTCTCCCAAGTCCACACAGGGGAGGTGATAGCATTGCTTTCGTGTAAATTATGTAATGCA CAGTCCTCTCCCAAGTCCACACAGGGGAGGTGGTAGCATTGCTTTCGTGTAAATTATGTAATGCA T C ACTB Ensembl:ENSG00000075624 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs546534519 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_685970,Human_RBP_ID_1052516,Human_RBP_ID_1114564,Human_RBP_ID_1332555,Human_RBP_ID_4944979,Human_RBP_ID_7746206,Human_RBP_ID_9211873,Human_RBP_ID_16179118,Human_RBP_ID_21396863,Human_RBP_ID_21904323,Human_RBP_ID_22407801,Human_RBP_ID_22516006,Human_RBP_ID_22835242,Human_RBP_ID_24219578,Human_RBP_ID_24516788,Human_RBP_ID_26547637,Human_RBP_ID_27114830,Human_RBP_ID_27358624 Human_miRNA_ID_2015439 RMVar_hsa_circ_77074,RMVar_hsa_circ_110714,RMVar_hsa_circ_126855,RMVar_hsa_circ_119696,RMVar_hsa_circ_96053,RMVar_hsa_circ_243503,RMVar_hsa_circ_243505,RMVar_hsa_circ_243506,RMVar_hsa_circ_243507,RMVar_hsa_circ_243504 47944 RMVar_ID_47944 Human_SNP_ID_308490850 A-to-I Human chr7 + 5601755 5601755 5601755 TCAGCTATTTGGGAGGCTGAGGTGGGAGGATCACTTGAGCCCAGGAAGTCGAGGCTACAGTGAGC TCAGCTATTTGGGAGGCTGAGGTGGGAGGATCTCTTGAGCCCAGGAAGTCGAGGCTACAGTGAGC A T FSCN1 Ensembl:ENSG00000075618 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs774899087 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 47945 RMVar_ID_47945 Human_SNP_ID_308490869 A-to-I Human chr7 + 5601827 5601827 5601827 GTGCCACTGCACTCCAACCTGGGCAACAGAGCAAGACCCTGAATCAAAAAGAAAGAGATGTATTT GTGCCACTGCACTCCAACCTGGGCAACAGAGCTAGACCCTGAATCAAAAAGAAAGAGATGTATTT A T FSCN1 Ensembl:ENSG00000075618 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1365728189 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 47946 RMVar_ID_47946 Human_SNP_ID_308490922 A-to-I Human chr7 + 5601973 5601973 5601973 GGGCTTAAAAAAAAATTTTTTTTTTTTTTTTGAGGCGGAATTTCATTCTTGTTGCCCAGGCTGGA GGGCTTAAAAAAAAATTTTTTTTTTTTTTTTGTGGCGGAATTTCATTCTTGTTGCCCAGGCTGGA A T FSCN1 Ensembl:ENSG00000075618 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285837285 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16181010 RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 47947 RMVar_ID_47947 Human_SNP_ID_308491218 A-to-I Human chr7 + 5602910 5602910 5602910 TGTAGAGACGGGGGTGGGGTGGGGGTCTTGCTATGTTGCCCAGGCTGGTCTCAAACTCCTAGACT TGTAGAGACGGGGGTGGGGTGGGGGTCTTGCTGTGTTGCCCAGGCTGGTCTCAAACTCCTAGACT A G FSCN1 Ensembl:ENSG00000075618 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1357650384 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22622407 RMVar_hsa_circ_102217,RMVar_hsa_circ_243469 47948 RMVar_ID_47948 Human_SNP_ID_308500781 A-to-I Human chr7 - 5630485 5630482 5630485 AGTCCCACCTACTCGGGGAGCCTAAGGTGAGAAGATCACTTGAGCCCAGGAGTTCAAGGCTGCAG AGTCCCACCTACTCGGGGAGCCTAAGGTGAGA___TCACTTGAGCCCAGGAGTTCAAGGCTGCAG ATCT A RNF216 Ensembl:ENSG00000011275 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1389973468 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_70487,RMVar_hsa_circ_305081 47949 RMVar_ID_47949 Human_SNP_ID_308501705 A-to-I Human chr7 - 5633319 5633319 5633319 CACCTGCCTAGGCCTCCCAAATTGCTGGGATTACAGGCATGAGCCACCGCACCCGGCCTTACTTC CACCTGCCTAGGCCTCCCAAATTGCTGGGATTGCAGGCATGAGCCACCGCACCCGGCCTTACTTC T C RNF216 Ensembl:ENSG00000011275 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1337775387 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70487,RMVar_hsa_circ_305081 47950 RMVar_ID_47950 Human_SNP_ID_308504346 A-to-I Human chr7 - 5641831 5641831 5641831 ACAGTTTCACCATGTTGGTCAGGCTGGTCTCAAACTCCTGAGCTCAAATGATCTTCCTGCTTTGG ACAGTTTCACCATGTTGGTCAGGCTGGTCTCAGACTCCTGAGCTCAAATGATCTTCCTGCTTTGG T C RNF216 Ensembl:ENSG00000011275 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1328545741 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56221,RMVar_hsa_circ_305081,RMVar_hsa_circ_273481,RMVar_hsa_circ_355082,RMVar_hsa_circ_377948,RMVar_hsa_circ_345777,RMVar_hsa_circ_275751,RMVar_hsa_circ_72654,RMVar_hsa_circ_243527,RMVar_hsa_circ_243528,RMVar_hsa_circ_243529 47951 RMVar_ID_47951 Human_SNP_ID_308504347 A-to-I Human chr7 - 5641832 5641832 5641832 GACAGTTTCACCATGTTGGTCAGGCTGGTCTCAAACTCCTGAGCTCAAATGATCTTCCTGCTTTG GACAGTTTCACCATGTTGGTCAGGCTGGTCTCGAACTCCTGAGCTCAAATGATCTTCCTGCTTTG T C RNF216 Ensembl:ENSG00000011275 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1434699790 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56221,RMVar_hsa_circ_305081,RMVar_hsa_circ_273481,RMVar_hsa_circ_355082,RMVar_hsa_circ_377948,RMVar_hsa_circ_345777,RMVar_hsa_circ_275751,RMVar_hsa_circ_72654,RMVar_hsa_circ_243527,RMVar_hsa_circ_243528,RMVar_hsa_circ_243529 47952 RMVar_ID_47952 Human_SNP_ID_308505857 A-to-I Human chr7 - 5646475 5646475 5646475 GTTAGCCAGGATAGTCTCGATCTCCGGACCTCATTATCTGCCCGCCTCTGCCTCCCAAGGTGCTG GTTAGCCAGGATAGTCTCGATCTCCGGACCTCGTTATCTGCCCGCCTCTGCCTCCCAAGGTGCTG T C RNF216 Ensembl:ENSG00000011275 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256462171 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56221,RMVar_hsa_circ_305081,RMVar_hsa_circ_273481,RMVar_hsa_circ_355082,RMVar_hsa_circ_377948,RMVar_hsa_circ_345777,RMVar_hsa_circ_275751,RMVar_hsa_circ_72654,RMVar_hsa_circ_243527,RMVar_hsa_circ_243528,RMVar_hsa_circ_243529 47953 RMVar_ID_47953 Human_SNP_ID_308506481 A-to-I Human chr7 - 5648388 5648388 5648388 TAAAATTTAGATCTAATCAGGCACAGTGGCTCACGCCTGTAACCCCAGCACTTTGGGAGGCTGAG TAAAATTTAGATCTAATCAGGCACAGTGGCTCGCGCCTGTAACCCCAGCACTTTGGGAGGCTGAG T C RNF216 Ensembl:ENSG00000011275 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1354039606 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56221,RMVar_hsa_circ_305081,RMVar_hsa_circ_273481,RMVar_hsa_circ_355082,RMVar_hsa_circ_377948,RMVar_hsa_circ_345777,RMVar_hsa_circ_275751,RMVar_hsa_circ_72654,RMVar_hsa_circ_243527,RMVar_hsa_circ_243528,RMVar_hsa_circ_243529 47954 RMVar_ID_47954 Human_SNP_ID_308506882 A-to-I Human chr7 - 5649503 5649503 5649503 ATGTCAAAACGTTTTTTTTCTCGCCTTGAGACAGTGTCTTATTCTGTCATCCAGGCTGGAATACA ATGTCAAAACGTTTTTTTTCTCGCCTTGAGACGGTGTCTTATTCTGTCATCCAGGCTGGAATACA T C RNF216 Ensembl:ENSG00000011275 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs547358106 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56221,RMVar_hsa_circ_305081,RMVar_hsa_circ_273481,RMVar_hsa_circ_355082,RMVar_hsa_circ_377948,RMVar_hsa_circ_345777,RMVar_hsa_circ_275751,RMVar_hsa_circ_72654,RMVar_hsa_circ_243527,RMVar_hsa_circ_243528,RMVar_hsa_circ_243529 47955 RMVar_ID_47955 Human_SNP_ID_308518564 A-to-I Human chr7 - 5686113 5686113 5686113 ATTCAAGCGATTCTCCTGCCTCAGCCTCCCGAATAGCTGGGATTACAGACGTGCATCACCACGCC ATTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGACGTGCATCACCACGCC T C RNF216 Ensembl:ENSG00000011275 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1428901991 Functional Loss SNV dbSNP153 33..33 33 - - - 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 47956 RMVar_ID_47956 Human_SNP_ID_308518582 A-to-I Human chr7 - 5686179 5686179 5686179 TACTCTGTCAACCCAGGCTGGAGTGCAGCAGCATGATCTCGGCTCACTGCAACCTCTGCCTTCTG TACTCTGTCAACCCAGGCTGGAGTGCAGCAGCGTGATCTCGGCTCACTGCAACCTCTGCCTTCTG T C RNF216 Ensembl:ENSG00000011275 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs370055013 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16181894 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 47957 RMVar_ID_47957 Human_SNP_ID_308528461 A-to-I Human chr7 - 5718259 5718259 5718259 CTCCTGCCTCAGCCACCTTAGTAGCTGGGATTACAGGTGCGCCCCACCATGCCTGGCTAATTTTT CTCCTGCCTCAGCCACCTTAGTAGCTGGGATTCCAGGTGCGCCCCACCATGCCTGGCTAATTTTT T G RNF216 Ensembl:ENSG00000011275 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1467621394 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5877,RMVar_hsa_circ_56221,RMVar_hsa_circ_355082,RMVar_hsa_circ_345777,RMVar_hsa_circ_275751,RMVar_hsa_circ_72654,RMVar_hsa_circ_302691,RMVar_hsa_circ_82528,RMVar_hsa_circ_243528,RMVar_hsa_circ_243529,RMVar_hsa_circ_17287,RMVar_hsa_circ_324998,RMVar_hsa_circ_243530,RMVar_hsa_circ_314667,RMVar_hsa_circ_107473,RMVar_hsa_circ_294854,RMVar_hsa_circ_275621,RMVar_hsa_circ_243532,RMVar_hsa_circ_9787,RMVar_hsa_circ_243533,RMVar_hsa_circ_243531,RMVar_hsa_circ_48422,RMVar_hsa_circ_283132,RMVar_hsa_circ_4557,RMVar_hsa_circ_346952,RMVar_hsa_circ_288692,RMVar_hsa_circ_243536,RMVar_hsa_circ_243537,RMVar_hsa_circ_342124,RMVar_hsa_circ_243538 47958 RMVar_ID_47958 Human_SNP_ID_308528594 A-to-I Human chr7 - 5718647 5718647 5718647 ACTTGGGAGGATGAGGCACGAGAATTGCTTGAACATGGGAGGTCGAGGTTGGTTGCAGTGAGCCA ACTTGGGAGGATGAGGCACGAGAATTGCTTGATCATGGGAGGTCGAGGTTGGTTGCAGTGAGCCA T A RNF216 Ensembl:ENSG00000011275 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7455961 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5877,RMVar_hsa_circ_56221,RMVar_hsa_circ_355082,RMVar_hsa_circ_345777,RMVar_hsa_circ_275751,RMVar_hsa_circ_72654,RMVar_hsa_circ_302691,RMVar_hsa_circ_82528,RMVar_hsa_circ_243528,RMVar_hsa_circ_243529,RMVar_hsa_circ_17287,RMVar_hsa_circ_324998,RMVar_hsa_circ_243530,RMVar_hsa_circ_314667,RMVar_hsa_circ_107473,RMVar_hsa_circ_294854,RMVar_hsa_circ_275621,RMVar_hsa_circ_243532,RMVar_hsa_circ_9787,RMVar_hsa_circ_243533,RMVar_hsa_circ_243531,RMVar_hsa_circ_48422,RMVar_hsa_circ_283132,RMVar_hsa_circ_4557,RMVar_hsa_circ_346952,RMVar_hsa_circ_288692,RMVar_hsa_circ_243536,RMVar_hsa_circ_243537,RMVar_hsa_circ_342124,RMVar_hsa_circ_243538 47959 RMVar_ID_47959 Human_SNP_ID_308528595 A-to-I Human chr7 - 5718647 5718647 5718647 ACTTGGGAGGATGAGGCACGAGAATTGCTTGAACATGGGAGGTCGAGGTTGGTTGCAGTGAGCCA ACTTGGGAGGATGAGGCACGAGAATTGCTTGACCATGGGAGGTCGAGGTTGGTTGCAGTGAGCCA T G RNF216 Ensembl:ENSG00000011275 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7455961 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5877,RMVar_hsa_circ_56221,RMVar_hsa_circ_355082,RMVar_hsa_circ_345777,RMVar_hsa_circ_275751,RMVar_hsa_circ_72654,RMVar_hsa_circ_302691,RMVar_hsa_circ_82528,RMVar_hsa_circ_243528,RMVar_hsa_circ_243529,RMVar_hsa_circ_17287,RMVar_hsa_circ_324998,RMVar_hsa_circ_243530,RMVar_hsa_circ_314667,RMVar_hsa_circ_107473,RMVar_hsa_circ_294854,RMVar_hsa_circ_275621,RMVar_hsa_circ_243532,RMVar_hsa_circ_9787,RMVar_hsa_circ_243533,RMVar_hsa_circ_243531,RMVar_hsa_circ_48422,RMVar_hsa_circ_283132,RMVar_hsa_circ_4557,RMVar_hsa_circ_346952,RMVar_hsa_circ_288692,RMVar_hsa_circ_243536,RMVar_hsa_circ_243537,RMVar_hsa_circ_342124,RMVar_hsa_circ_243538 47960 RMVar_ID_47960 Human_SNP_ID_308529514 A-to-I Human chr7 - 5721521 5721521 5721521 AATTGCGGACATACATTCACCAACAAATGGCTATAAGCAGCGCTATTCAGATTAACCCAAAACAG AATTGCGGACATACATTCACCAACAAATGGCTGTAAGCAGCGCTATTCAGATTAACCCAAAACAG T C RNF216 Ensembl:ENSG00000011275 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1990836 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5799,GWAS_ID_5800,GWAS_ID_5801,GWAS_ID_5802,GWAS_ID_5803 RMVar_hsa_circ_5877,RMVar_hsa_circ_56221,RMVar_hsa_circ_355082,RMVar_hsa_circ_275751,RMVar_hsa_circ_72654,RMVar_hsa_circ_302691,RMVar_hsa_circ_82528,RMVar_hsa_circ_243529,RMVar_hsa_circ_17287,RMVar_hsa_circ_324998,RMVar_hsa_circ_243530,RMVar_hsa_circ_314667,RMVar_hsa_circ_107473,RMVar_hsa_circ_275621,RMVar_hsa_circ_243532,RMVar_hsa_circ_9787,RMVar_hsa_circ_243533,RMVar_hsa_circ_243531,RMVar_hsa_circ_283132,RMVar_hsa_circ_4557,RMVar_hsa_circ_288692,RMVar_hsa_circ_243537,RMVar_hsa_circ_342124,RMVar_hsa_circ_243539,RMVar_hsa_circ_347438,RMVar_hsa_circ_358070,RMVar_hsa_circ_315138 47961 RMVar_ID_47961 Human_SNP_ID_308529515 A-to-I Human chr7 - 5721521 5721521 5721521 AATTGCGGACATACATTCACCAACAAATGGCTATAAGCAGCGCTATTCAGATTAACCCAAAACAG AATTGCGGACATACATTCACCAACAAATGGCTCTAAGCAGCGCTATTCAGATTAACCCAAAACAG T G RNF216 Ensembl:ENSG00000011275 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1990836 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5799,GWAS_ID_5800,GWAS_ID_5801,GWAS_ID_5802,GWAS_ID_5803 RMVar_hsa_circ_5877,RMVar_hsa_circ_56221,RMVar_hsa_circ_355082,RMVar_hsa_circ_275751,RMVar_hsa_circ_72654,RMVar_hsa_circ_302691,RMVar_hsa_circ_82528,RMVar_hsa_circ_243529,RMVar_hsa_circ_17287,RMVar_hsa_circ_324998,RMVar_hsa_circ_243530,RMVar_hsa_circ_314667,RMVar_hsa_circ_107473,RMVar_hsa_circ_275621,RMVar_hsa_circ_243532,RMVar_hsa_circ_9787,RMVar_hsa_circ_243533,RMVar_hsa_circ_243531,RMVar_hsa_circ_283132,RMVar_hsa_circ_4557,RMVar_hsa_circ_288692,RMVar_hsa_circ_243537,RMVar_hsa_circ_342124,RMVar_hsa_circ_243539,RMVar_hsa_circ_347438,RMVar_hsa_circ_358070,RMVar_hsa_circ_315138 47962 RMVar_ID_47962 Human_SNP_ID_308529991 A-to-I Human chr7 - 5722839 5722839 5722839 GGTGTGCGCCATCATGCCTGGGGGGTTTCACCATGTTGGACAGGTTGGTCTCGAACTCCTAACCT GGTGTGCGCCATCATGCCTGGGGGGTTTCACCGTGTTGGACAGGTTGGTCTCGAACTCCTAACCT T C RNF216 Ensembl:ENSG00000011275 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs778404252 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5877,RMVar_hsa_circ_56221,RMVar_hsa_circ_355082,RMVar_hsa_circ_275751,RMVar_hsa_circ_72654,RMVar_hsa_circ_302691,RMVar_hsa_circ_82528,RMVar_hsa_circ_243529,RMVar_hsa_circ_17287,RMVar_hsa_circ_324998,RMVar_hsa_circ_243530,RMVar_hsa_circ_314667,RMVar_hsa_circ_107473,RMVar_hsa_circ_275621,RMVar_hsa_circ_243532,RMVar_hsa_circ_9787,RMVar_hsa_circ_243533,RMVar_hsa_circ_243531,RMVar_hsa_circ_283132,RMVar_hsa_circ_4557,RMVar_hsa_circ_288692,RMVar_hsa_circ_243537,RMVar_hsa_circ_342124,RMVar_hsa_circ_243539,RMVar_hsa_circ_347438,RMVar_hsa_circ_358070,RMVar_hsa_circ_315138 47963 RMVar_ID_47963 Human_SNP_ID_308535644 A-to-I Human chr7 - 5739891 5739891 5739891 TCAAGCGATTCTTCTGTCTCTGCCTCCCGAGTAGCTGGGATCACAGGCACATACCACCACGTCTG TCAAGCGATTCTTCTGTCTCTGCCTCCCGAGTTGCTGGGATCACAGGCACATACCACCACGTCTG T A RNF216 Ensembl:ENSG00000011275 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs371726176 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5877,RMVar_hsa_circ_72654,RMVar_hsa_circ_302691,RMVar_hsa_circ_324998,RMVar_hsa_circ_107473,RMVar_hsa_circ_243532,RMVar_hsa_circ_243531,RMVar_hsa_circ_335127,RMVar_hsa_circ_335132,RMVar_hsa_circ_243541,RMVar_hsa_circ_243543,RMVar_hsa_circ_312403,RMVar_hsa_circ_281539,RMVar_hsa_circ_289894,RMVar_hsa_circ_243542,RMVar_hsa_circ_282355,RMVar_hsa_circ_243544,RMVar_hsa_circ_243545 47964 RMVar_ID_47964 Human_SNP_ID_308535645 A-to-I Human chr7 - 5739891 5739891 5739891 TCAAGCGATTCTTCTGTCTCTGCCTCCCGAGTAGCTGGGATCACAGGCACATACCACCACGTCTG TCAAGCGATTCTTCTGTCTCTGCCTCCCGAGTGGCTGGGATCACAGGCACATACCACCACGTCTG T C RNF216 Ensembl:ENSG00000011275 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs371726176 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5877,RMVar_hsa_circ_72654,RMVar_hsa_circ_302691,RMVar_hsa_circ_324998,RMVar_hsa_circ_107473,RMVar_hsa_circ_243532,RMVar_hsa_circ_243531,RMVar_hsa_circ_335127,RMVar_hsa_circ_335132,RMVar_hsa_circ_243541,RMVar_hsa_circ_243543,RMVar_hsa_circ_312403,RMVar_hsa_circ_281539,RMVar_hsa_circ_289894,RMVar_hsa_circ_243542,RMVar_hsa_circ_282355,RMVar_hsa_circ_243544,RMVar_hsa_circ_243545 47965 RMVar_ID_47965 Human_SNP_ID_308543790 A-to-I Human chr7 - 5763945 5763945 5763945 ACCTCGAGTGATCCGCCTGCCTCGGCCTCCCAAGGTGCTTAGATTACAGCCATGAGCTGTCGTGC ACCTCGAGTGATCCGCCTGCCTCGGCCTCCCAGGGTGCTTAGATTACAGCCATGAGCTGTCGTGC T C RNF216 Ensembl:ENSG00000011275 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1002875083 Functional Loss SNV dbSNP153 33..33 33 - - - 47966 RMVar_ID_47966 Human_SNP_ID_308547822 A-to-I Human chr7 - 5774826 5774826 5774826 TTGAACTCTGGAGGGGATGTTGCAGTGAACTGAGATTGCACCATTGCACTCCAGCCTGGGCAACA TTGAACTCTGGAGGGGATGTTGCAGTGAACTGCGATTGCACCATTGCACTCCAGCCTGGGCAACA T G RNF216 Ensembl:ENSG00000011275 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs567572277 Functional Loss SNV dbSNP153 33..33 33 - - - 47967 RMVar_ID_47967 Human_SNP_ID_308547824 A-to-I Human chr7 - 5774830 5774830 5774830 TCACTTGAACTCTGGAGGGGATGTTGCAGTGAACTGAGATTGCACCATTGCACTCCAGCCTGGGC TCACTTGAACTCTGGAGGGGATGTTGCAGTGAGCTGAGATTGCACCATTGCACTCCAGCCTGGGC T C RNF216 Ensembl:ENSG00000011275 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1007344050 Functional Loss SNV dbSNP153 33..33 33 - - - 47968 RMVar_ID_47968 Human_SNP_ID_308577343 A-to-I Human chr7 + 5843247 5843246 5843248 ATGGTGGCATGTGCCTATAGTGTCATCTAATCAGGGGACTGAGGGGAGAGGATCACTTGAGCCCA ATGGTGGCATGTGCCTATAGTGTCATCTAATC__GGGACTGAGGGGAGAGGATCACTTGAGCCCA CAG C ZNF815P Ensembl:ENSG00000235944 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031068539 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_82207,RMVar_hsa_circ_243553,RMVar_hsa_circ_243554 47969 RMVar_ID_47969 Human_SNP_ID_308577344 A-to-I Human chr7 + 5843247 5843246 5843247 ATGGTGGCATGTGCCTATAGTGTCATCTAATCAGGGGACTGAGGGGAGAGGATCACTTGAGCCCA ATGGTGGCATGTGCCTATAGTGTCATCTAATC_GGGGACTGAGGGGAGAGGATCACTTGAGCCCA CA C ZNF815P Ensembl:ENSG00000235944 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1374632776 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_82207,RMVar_hsa_circ_243553,RMVar_hsa_circ_243554 47970 RMVar_ID_47970 Human_SNP_ID_308579358 A-to-I Human chr7 + 5848116 5848116 5848116 AATTCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGGTTGAACCTGGGAGGCGGAGATTGCAGT AATTCCAGCTACTCGGGAGGCTGAGGCAGGAGGATCGGTTGAACCTGGGAGGCGGAGATTGCAGT A G ZNF815P Ensembl:ENSG00000235944 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1390374309 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_82207,RMVar_hsa_circ_243553,RMVar_hsa_circ_243554 47971 RMVar_ID_47971 Human_SNP_ID_308579439 A-to-I Human chr7 + 5848305 5848305 5848305 ATCTATTTTCGTAGGTGTACTTTTTTTTTTTGAGACGGAGTCCTCGTTCTATCGCCCAGTCTGGA ATCTATTTTCGTAGGTGTACTTTTTTTTTTTGGGACGGAGTCCTCGTTCTATCGCCCAGTCTGGA A G ZNF815P Ensembl:ENSG00000235944 Pseudogene intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1207993332 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_82207,RMVar_hsa_circ_243553,RMVar_hsa_circ_243554 47972 RMVar_ID_47972 Human_SNP_ID_308579452 A-to-I Human chr7 + 5848323 5848323 5848323 ACTTTTTTTTTTTGAGACGGAGTCCTCGTTCTATCGCCCAGTCTGGAGGGCAGTGGTGCCATCTC ACTTTTTTTTTTTGAGACGGAGTCCTCGTTCTGTCGCCCAGTCTGGAGGGCAGTGGTGCCATCTC A G ZNF815P Ensembl:ENSG00000235944 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs567678476 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_82207,RMVar_hsa_circ_243553,RMVar_hsa_circ_243554 47973 RMVar_ID_47973 Human_SNP_ID_308579471 A-to-I Human chr7 + 5848361 5848361 5848361 CAGTCTGGAGGGCAGTGGTGCCATCTCGGCTCACTGCAGCCTCTGCCTCCCGGGTTCATGTGATT CAGTCTGGAGGGCAGTGGTGCCATCTCGGCTCTCTGCAGCCTCTGCCTCCCGGGTTCATGTGATT A T ZNF815P Ensembl:ENSG00000235944 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1364471968 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_82207,RMVar_hsa_circ_243553,RMVar_hsa_circ_243554 47974 RMVar_ID_47974 Human_SNP_ID_308579519 A-to-I Human chr7 + 5848471 5848471 5848471 AGCGTGCCGGGCCAATTTTTTGTGTTTTTAGTAGAGATGGAGTTTCACCATGTTGGTCAGGCTGT AGCGTGCCGGGCCAATTTTTTGTGTTTTTAGTGGAGATGGAGTTTCACCATGTTGGTCAGGCTGT A G ZNF815P Ensembl:ENSG00000235944 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1008572571 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_82207,RMVar_hsa_circ_243553,RMVar_hsa_circ_243554 47975 RMVar_ID_47975 Human_SNP_ID_308579524 A-to-I Human chr7 + 5848488 5848488 5848488 TTTTGTGTTTTTAGTAGAGATGGAGTTTCACCATGTTGGTCAGGCTGTTCTCGAACTCCTGACCT TTTTGTGTTTTTAGTAGAGATGGAGTTTCACCGTGTTGGTCAGGCTGTTCTCGAACTCCTGACCT A G ZNF815P Ensembl:ENSG00000235944 Pseudogene intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1200505388 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_82207,RMVar_hsa_circ_243553,RMVar_hsa_circ_243554 47976 RMVar_ID_47976 Human_SNP_ID_308579546 A-to-I Human chr7 + 5848533 5848533 5848533 TGTTCTCGAACTCCTGACCTCATGATCTGCCCACCTCAGCTTCCCAAAGTGCTGGGATTACAGGC TGTTCTCGAACTCCTGACCTCATGATCTGCCCTCCTCAGCTTCCCAAAGTGCTGGGATTACAGGC A T ZNF815P Ensembl:ENSG00000235944 Pseudogene intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1464173486 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_82207,RMVar_hsa_circ_243553,RMVar_hsa_circ_243554 47977 RMVar_ID_47977 Human_SNP_ID_308579839 A-to-I Human chr7 + 5849273 5849273 5849273 GGGAGGCTCAGGCACGAGAATTGCTTGAGCCCAGCAGGCAGAGGTTGCAGTGAGCTGAGATTGTG GGGAGGCTCAGGCACGAGAATTGCTTGAGCCCTGCAGGCAGAGGTTGCAGTGAGCTGAGATTGTG A T ZNF815P Ensembl:ENSG00000235944 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs528139926 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18540411 RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_82207,RMVar_hsa_circ_243553,RMVar_hsa_circ_243554 47978 RMVar_ID_47978 Human_SNP_ID_308579845 A-to-I Human chr7 + 5849280 5849280 5849280 TCAGGCACGAGAATTGCTTGAGCCCAGCAGGCAGAGGTTGCAGTGAGCTGAGATTGTGCCACTTC TCAGGCACGAGAATTGCTTGAGCCCAGCAGGCGGAGGTTGCAGTGAGCTGAGATTGTGCCACTTC A G ZNF815P Ensembl:ENSG00000235944 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1020195053 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18540411 RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_82207,RMVar_hsa_circ_243553,RMVar_hsa_circ_243554 47979 RMVar_ID_47979 Human_SNP_ID_308579920 A-to-I Human chr7 + 5849464 5849464 5849464 TCGTGCCTGTGATCTCAGCACTTGGGAAAGTCAAGGTGGACAGGTCACTTGACCCCAGGAGTTCA TCGTGCCTGTGATCTCAGCACTTGGGAAAGTCGAGGTGGACAGGTCACTTGACCCCAGGAGTTCA A G ZNF815P Ensembl:ENSG00000235944 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903110709 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_82207,RMVar_hsa_circ_243553,RMVar_hsa_circ_243554,RMVar_hsa_circ_243555 47980 RMVar_ID_47980 Human_SNP_ID_308579949 A-to-I Human chr7 + 5849536 5849536 5849536 CCTGGGCAACACGGTGAGACCCTGTCTGTACCAAATACATATATATATTAGCTGGGCGTGGTGGC CCTGGGCAACACGGTGAGACCCTGTCTGTACCGAATACATATATATATTAGCTGGGCGTGGTGGC A G ZNF815P Ensembl:ENSG00000235944 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1175473768 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_243554,RMVar_hsa_circ_243555 47981 RMVar_ID_47981 Human_SNP_ID_308579991 A-to-I Human chr7 + 5849625 5849625 5849625 GGGAGGCTGAGGTGGGAGAATCCCTTGAGCCCAGGAGTTTGAGGCTACAGTGAGCCATGGTCGTG GGGAGGCTGAGGTGGGAGAATCCCTTGAGCCCCGGAGTTTGAGGCTACAGTGAGCCATGGTCGTG A C ZNF815P Ensembl:ENSG00000235944 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs552887213 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5251211 RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_243554,RMVar_hsa_circ_243555 47982 RMVar_ID_47982 Human_SNP_ID_308579992 A-to-I Human chr7 + 5849625 5849625 5849625 GGGAGGCTGAGGTGGGAGAATCCCTTGAGCCCAGGAGTTTGAGGCTACAGTGAGCCATGGTCGTG GGGAGGCTGAGGTGGGAGAATCCCTTGAGCCCGGGAGTTTGAGGCTACAGTGAGCCATGGTCGTG A G ZNF815P Ensembl:ENSG00000235944 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs552887213 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5251211 RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_243554,RMVar_hsa_circ_243555 47983 RMVar_ID_47983 Human_SNP_ID_308579997 A-to-I Human chr7 + 5849639 5849639 5849639 GGAGAATCCCTTGAGCCCAGGAGTTTGAGGCTACAGTGAGCCATGGTCGTGCCACTGCGCACCAG GGAGAATCCCTTGAGCCCAGGAGTTTGAGGCTGCAGTGAGCCATGGTCGTGCCACTGCGCACCAG A G ZNF815P Ensembl:ENSG00000235944 Pseudogene intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs982011999 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5251211 RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_243554,RMVar_hsa_circ_243555 47984 RMVar_ID_47984 Human_SNP_ID_308580283 A-to-I Human chr7 + 5850325 5850325 5850325 GGGCGTGATGGCAGACGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGACTTCGCTCGA GGGCGTGATGGCAGACGCCTGTAGTCCCAGCTGCTCGGGAGGCTGAGGCAGGAGACTTCGCTCGA A G ZNF815P Ensembl:ENSG00000235944 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934235003 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_243554,RMVar_hsa_circ_243555 47985 RMVar_ID_47985 Human_SNP_ID_308581047 A-to-I Human chr7 + 5852112 5852112 5852112 CATGGTGAAACCCTGTCTCTACAAAAAAAATTAGCCGGACGTGGTAGCATGTGCCTGCAGTCCCA CATGGTGAAACCCTGTCTCTACAAAAAAAATTGGCCGGACGTGGTAGCATGTGCCTGCAGTCCCA A G ZNF815P Ensembl:ENSG00000235944 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs921627108 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_243554,RMVar_hsa_circ_243555 47986 RMVar_ID_47986 Human_SNP_ID_308601662 A-to-I Human chr7 + 5911478 5911478 5911478 GTGTGTGCCACCACACCTGGCTAATTTTTTGTAGAGATGGGATCTCGTCATGTTGCCCAGGCTAT GTGTGTGCCACCACACCTGGCTAATTTTTTGTCGAGATGGGATCTCGTCATGTTGCCCAGGCTAT A C CCZ1 Ensembl:ENSG00000122674 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1158597740 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10355720,Human_RBP_ID_23077379 RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_4764,RMVar_hsa_circ_43290,RMVar_hsa_circ_356243,RMVar_hsa_circ_243558,RMVar_hsa_circ_75622,RMVar_hsa_circ_283728,RMVar_hsa_circ_243556,RMVar_hsa_circ_100861,RMVar_hsa_circ_340332,RMVar_hsa_circ_311578,RMVar_hsa_circ_299225,RMVar_hsa_circ_283599,RMVar_hsa_circ_243559,RMVar_hsa_circ_73187,RMVar_hsa_circ_319524,RMVar_hsa_circ_243557,RMVar_hsa_circ_335342,RMVar_hsa_circ_313590,RMVar_hsa_circ_305587,RMVar_hsa_circ_268306,RMVar_hsa_circ_120193,RMVar_hsa_circ_325819,RMVar_hsa_circ_243566,RMVar_hsa_circ_328635,RMVar_hsa_circ_346007,RMVar_hsa_circ_326680,RMVar_hsa_circ_243567,RMVar_hsa_circ_90238 47987 RMVar_ID_47987 Human_SNP_ID_308616783 A-to-I Human chr7 - 5977258 5977258 5977258 GAGTTCAGGAGATCGAGACCATCCTGGCTAACATGGTGAAAGCCCGTCTCTACTAAAAATACAAA GAGTTCAGGAGATCGAGACCATCCTGGCTAACGTGGTGAAAGCCCGTCTCTACTAAAAATACAAA T C PMS2 Ensembl:ENSG00000122512 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs188558508 Functional Loss SNV dbSNP153 33..33 33 - - - 47988 RMVar_ID_47988 Human_SNP_ID_308617716 A-to-I Human chr7 - 5979802 5979802 5979802 TATCCAGCACTCAGGACCAGATGCAGTGGCTCACACTCGTAATCCCAGCACTTTGGGAGGCTGAA TATCCAGCACTCAGGACCAGATGCAGTGGCTCGCACTCGTAATCCCAGCACTTTGGGAGGCTGAA T C PMS2 Ensembl:ENSG00000122512 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1386163476 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_243570,RMVar_hsa_circ_285647,RMVar_hsa_circ_318372,RMVar_hsa_circ_339010,RMVar_hsa_circ_26027,RMVar_hsa_circ_346977 47989 RMVar_ID_47989 Human_SNP_ID_308622028 A-to-I Human chr7 - 5993174 5993174 5993174 TAGAGATGGGGTTTCACTGTGTTGCCCAGGCTAGTCAAGAACTCCTGAGCTCAGGCAATCCACCT TAGAGATGGGGTTTCACTGTGTTGCCCAGGCTGGTCAAGAACTCCTGAGCTCAGGCAATCCACCT T C PMS2 Ensembl:ENSG00000122512 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1191906842 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26027,RMVar_hsa_circ_346300,RMVar_hsa_circ_354815,RMVar_hsa_circ_123100,RMVar_hsa_circ_47228,RMVar_hsa_circ_243572,RMVar_hsa_circ_310450,RMVar_hsa_circ_311909,RMVar_hsa_circ_354867,RMVar_hsa_circ_367226,RMVar_hsa_circ_64052,RMVar_hsa_circ_243574,RMVar_hsa_circ_243575,RMVar_hsa_circ_62213 47990 RMVar_ID_47990 Human_SNP_ID_308622481 A-to-I Human chr7 - 5994342 5994342 5994342 GAGTCTCGCCCTGTTGGCCAGTCTGGAGTGCAATGGTGCGATTTTGGCTCACTGCAACCTCCACC GAGTCTCGCCCTGTTGGCCAGTCTGGAGTGCAGTGGTGCGATTTTGGCTCACTGCAACCTCCACC T C PMS2 Ensembl:ENSG00000122512 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs192381426 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26027,RMVar_hsa_circ_346300,RMVar_hsa_circ_354815,RMVar_hsa_circ_123100,RMVar_hsa_circ_47228,RMVar_hsa_circ_243572,RMVar_hsa_circ_310450,RMVar_hsa_circ_311909,RMVar_hsa_circ_354867,RMVar_hsa_circ_367226,RMVar_hsa_circ_64052,RMVar_hsa_circ_243574,RMVar_hsa_circ_243575,RMVar_hsa_circ_62213 47991 RMVar_ID_47991 Human_SNP_ID_308622862 A-to-I Human chr7 - 5995326 5995326 5995326 TGTTTCAACTGAAGACTTTTCTGTCCGGGCGCAGTGGCTCATGCCTGTAATCCCAGCACTTTGGG TGTTTCAACTGAAGACTTTTCTGTCCGGGCGCCGTGGCTCATGCCTGTAATCCCAGCACTTTGGG T G PMS2 Ensembl:ENSG00000122512 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1375166699 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16183126 RMVar_hsa_circ_26027,RMVar_hsa_circ_346300,RMVar_hsa_circ_354815,RMVar_hsa_circ_123100,RMVar_hsa_circ_47228,RMVar_hsa_circ_243572,RMVar_hsa_circ_310450,RMVar_hsa_circ_311909,RMVar_hsa_circ_354867,RMVar_hsa_circ_367226,RMVar_hsa_circ_64052,RMVar_hsa_circ_243574,RMVar_hsa_circ_243575,RMVar_hsa_circ_62213 47992 RMVar_ID_47992 Human_SNP_ID_308627559 A-to-I Human chr7 - 6008487 6008487 6008487 CCTTGGCCCCTCAAAGTGCTGGAATTAAAGGCATGATGCACCGTGCCTGGCCTTTTTAAAAAATT CCTTGGCCCCTCAAAGTGCTGGAATTAAAGGCGTGATGCACCGTGCCTGGCCTTTTTAAAAAATT T C PMS2 Ensembl:ENSG00000122512 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1388166044 Functional Loss SNV dbSNP153 33..33 33 - - - 47993 RMVar_ID_47993 Human_SNP_ID_308628540 A-to-I Human chr7 + 6010109 6010109 6010109 TCCCAAGAGTTTGAGACCACTCTCAGCAACATAGCGAGACCCTTGTCTCTATTTTTTAAATGTTT TCCCAAGAGTTTGAGACCACTCTCAGCAACATGGCGAGACCCTTGTCTCTATTTTTTAAATGTTT A G AIMP2 Ensembl:ENSG00000106305 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs543583156 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18171712 RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_243583,RMVar_hsa_circ_105021 47994 RMVar_ID_47994 Human_SNP_ID_308628708 A-to-I Human chr7 + 6010692 6010692 6010692 GCTGATCTCGAACTCCTGACCTCAAGAGATCCACCCGCCTCGACCTCCCAAAGTGTTGGGATTAC GCTGATCTCGAACTCCTGACCTCAAGAGATCCCCCCGCCTCGACCTCCCAAAGTGTTGGGATTAC A C AIMP2 Ensembl:ENSG00000106305 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs954197642 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_243583,RMVar_hsa_circ_105021 47995 RMVar_ID_47995 Human_SNP_ID_308629150 A-to-I Human chr7 + 6012178 6012178 6012178 AGGAGGCTGAGGTGGGAGGATCACTTGAGCCCAGGAGGTCAGGGCTGCATTGAGCTGTGATCCTG AGGAGGCTGAGGTGGGAGGATCACTTGAGCCCGGGAGGTCAGGGCTGCATTGAGCTGTGATCCTG A G AIMP2 Ensembl:ENSG00000106305 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs978609229 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_243583,RMVar_hsa_circ_105021 47996 RMVar_ID_47996 Human_SNP_ID_308629283 A-to-I Human chr7 + 6012581 6012580 6012582 TTCCTGACCGAGGTTTTTTTTGTTTTTGAGACAGAGTCTCACTCTGTCACCCAGTCTGGAGTGCA TTCCTGACCGAGGTTTTTTTTGTTTTTGAGAC__AGTCTCACTCTGTCACCCAGTCTGGAGTGCA CAG C AIMP2 Ensembl:ENSG00000106305 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs775387624 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_243583,RMVar_hsa_circ_105021 47997 RMVar_ID_47997 Human_SNP_ID_308629285 A-to-I Human chr7 + 6012589 6012589 6012589 CGAGGTTTTTTTTGTTTTTGAGACAGAGTCTCACTCTGTCACCCAGTCTGGAGTGCAATGTCGCA CGAGGTTTTTTTTGTTTTTGAGACAGAGTCTCGCTCTGTCACCCAGTCTGGAGTGCAATGTCGCA A G AIMP2 Ensembl:ENSG00000106305 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs148315304 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_243583,RMVar_hsa_circ_105021 47998 RMVar_ID_47998 Human_SNP_ID_308629286 A-to-I Human chr7 + 6012589 6012589 6012589 CGAGGTTTTTTTTGTTTTTGAGACAGAGTCTCACTCTGTCACCCAGTCTGGAGTGCAATGTCGCA CGAGGTTTTTTTTGTTTTTGAGACAGAGTCTCTCTCTGTCACCCAGTCTGGAGTGCAATGTCGCA A T AIMP2 Ensembl:ENSG00000106305 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs148315304 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_243583,RMVar_hsa_circ_105021 47999 RMVar_ID_47999 Human_SNP_ID_308629353 A-to-I Human chr7 + 6012739 6012739 6012739 CCCCCACCAAGCCCAGCTAATTTTTGTGTTTCAGTAGAAATGGAGTTTCATCATGTTGTCCTCTC CCCCCACCAAGCCCAGCTAATTTTTGTGTTTCGGTAGAAATGGAGTTTCATCATGTTGTCCTCTC A G AIMP2 Ensembl:ENSG00000106305 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs952130737 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16183270 Human_Splice_Rec_841598 RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_243583,RMVar_hsa_circ_105021 48000 RMVar_ID_48000 Human_SNP_ID_308629376 A-to-I Human chr7 + 6012795 6012795 6012795 TGTCCTCTCGAACTCCTGACCTCAAGTGATCCACCCGCCTCGCCCTTCCAAAGTGCTGAGATTAC TGTCCTCTCGAACTCCTGACCTCAAGTGATCCCCCCGCCTCGCCCTTCCAAAGTGCTGAGATTAC A C AIMP2 Ensembl:ENSG00000106305 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs891527046 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_243583,RMVar_hsa_circ_105021 48001 RMVar_ID_48001 Human_SNP_ID_308629565 A-to-I Human chr7 + 6013361 6013361 6013361 TCTGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGAATAGC TCTGCTCACTGCAACCTCCGCCTCCCGGGTTCCAGCGATTCTCCTGCCTCAGCCTCCTGAATAGC A C AIMP2 Ensembl:ENSG00000106305 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs987220718 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_243583,RMVar_hsa_circ_105021 48002 RMVar_ID_48002 Human_SNP_ID_308629572 A-to-I Human chr7 + 6013379 6013379 6013379 CGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGAATAGCTGGTATTACAGGCACCCA CGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCCGCCTCCTGAATAGCTGGTATTACAGGCACCCA A C AIMP2 Ensembl:ENSG00000106305 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1425389384 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_243583,RMVar_hsa_circ_105021 48003 RMVar_ID_48003 Human_SNP_ID_308629694 A-to-I Human chr7 + 6013738 6013738 6013738 TGGGACCTGAGGTGGGAGGATGGCTTGAGGACAGGAGTTTGAGACCAGCCTGAGCAACATAGCGC TGGGACCTGAGGTGGGAGGATGGCTTGAGGACGGGAGTTTGAGACCAGCCTGAGCAACATAGCGC A G AIMP2 Ensembl:ENSG00000106305 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1489326829 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_253199,Human_RBP_ID_16183307 RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_243583,RMVar_hsa_circ_105021 48004 RMVar_ID_48004 Human_SNP_ID_308629720 A-to-I Human chr7 + 6013844 6013844 6013844 TTGGTGGCACACACTTGTAGTCCCAGGCACTCAGGAGACTAAGGCAGGAGGATCACTTGAGCCCA TTGGTGGCACACACTTGTAGTCCCAGGCACTCGGGAGACTAAGGCAGGAGGATCACTTGAGCCCA A G AIMP2 Ensembl:ENSG00000106305 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1488494945 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_243583,RMVar_hsa_circ_105021 48005 RMVar_ID_48005 Human_SNP_ID_308632242 A-to-I Human chr7 + 6020917 6020917 6020917 TGATCAGGCGAGCTCTTACCTATAAAACTGCTAACACCTGAGACTTAACGGGAAAAGATAAACAC TGATCAGGCGAGCTCTTACCTATAAAACTGCTGACACCTGAGACTTAACGGGAAAAGATAAACAC A G AIMP2 Ensembl:ENSG00000106305 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1230847649 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2528189 RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_243583,RMVar_hsa_circ_105021 48006 RMVar_ID_48006 Human_SNP_ID_308635196 A-to-I Human chr7 - 6029923 6029923 6029923 CAGGCTGGAGTGCAGTGATGCGATCTCGTCTCACTGCAACCTCTGCCTCCCAGGTTCAAGCAATT CAGGCTGGAGTGCAGTGATGCGATCTCGTCTCGCTGCAACCTCTGCCTCCCAGGTTCAAGCAATT T C EIF2AK1 Ensembl:ENSG00000086232 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1055457663 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36018,RMVar_hsa_circ_358976,RMVar_hsa_circ_29677,RMVar_hsa_circ_267125,RMVar_hsa_circ_65988 48007 RMVar_ID_48007 Human_SNP_ID_308661150 A-to-I Human chr7 + 6108003 6108003 6108003 CTAGTTAAAAATTACACCAGCCTGGCCAACATAGTGAAACCCGGCTCCACTAAAAATACAAAAAT CTAGTTAAAAATTACACCAGCCTGGCCAACATGGTGAAACCCGGCTCCACTAAAAATACAAAAAT A G USP42 Ensembl:ENSG00000106346 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1173028681 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_94958,RMVar_hsa_circ_243600 48008 RMVar_ID_48008 Human_SNP_ID_308664080 A-to-I Human chr7 + 6116079 6116079 6116079 TGAGCTGTGATCGCACTGCTGTACTTCAGCCTAGACAACAGAAAGAGACCCTGTCTCAAAAAAAA TGAGCTGTGATCGCACTGCTGTACTTCAGCCTCGACAACAGAAAGAGACCCTGTCTCAAAAAAAA A C USP42 Ensembl:ENSG00000106346 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1481724430 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_42280,RMVar_hsa_circ_94958,RMVar_hsa_circ_318028,RMVar_hsa_circ_322323,RMVar_hsa_circ_243600,RMVar_hsa_circ_327569,RMVar_hsa_circ_243602,RMVar_hsa_circ_7123,RMVar_hsa_circ_13010,RMVar_hsa_circ_287056,RMVar_hsa_circ_339414,RMVar_hsa_circ_243601,RMVar_hsa_circ_313763,RMVar_hsa_circ_274785,RMVar_hsa_circ_243606,RMVar_hsa_circ_243607,RMVar_hsa_circ_243605 48009 RMVar_ID_48009 Human_SNP_ID_308707973 A-to-I Human chr7 - 6244589 6244589 6244589 GTGATGGTGTATACTGGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGGATCGCTTGAGTCCA GTGATGGTGTATACTGGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGGATCGCTTGAGTCCA T C CYTH3 Ensembl:ENSG00000008256 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1253166120 Functional Loss SNV dbSNP153 33..33 33 - - - 48010 RMVar_ID_48010 Human_SNP_ID_308710812 A-to-I Human chr7 - 6253482 6253482 6253482 TTTGGTGGCTGGGTGCGATGGATCAGGCTGGTAATTTCAGCACTTTGAGAGGCCGAGGCAGGCGG TTTGGTGGCTGGGTGCGATGGATCAGGCTGGTTATTTCAGCACTTTGAGAGGCCGAGGCAGGCGG T A CYTH3 Ensembl:ENSG00000008256 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1056480700 Functional Loss SNV dbSNP153 33..33 33 - - - 48011 RMVar_ID_48011 Human_SNP_ID_308710813 A-to-I Human chr7 - 6253482 6253482 6253482 TTTGGTGGCTGGGTGCGATGGATCAGGCTGGTAATTTCAGCACTTTGAGAGGCCGAGGCAGGCGG TTTGGTGGCTGGGTGCGATGGATCAGGCTGGTCATTTCAGCACTTTGAGAGGCCGAGGCAGGCGG T G CYTH3 Ensembl:ENSG00000008256 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1056480700 Functional Loss SNV dbSNP153 33..33 33 - - - 48012 RMVar_ID_48012 Human_SNP_ID_308710959 A-to-I Human chr7 - 6253810 6253810 6253810 TTTGTTTATTTATTTATTTTTATTTTTGAGACAGCATCTCACTCTGTCACCCAGGCTGGAGTGCA TTTGTTTATTTATTTATTTTTATTTTTGAGACGGCATCTCACTCTGTCACCCAGGCTGGAGTGCA T C CYTH3 Ensembl:ENSG00000008256 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs889757511 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16184582 48013 RMVar_ID_48013 Human_SNP_ID_308755068 A-to-I Human chr7 + 6382648 6382648 6382648 CACTTTGGGAGGCCGATGGGGTGGATCTCCTGAGGTCAGGAATTCGAGACCAGTCTGGCCAACAT CACTTTGGGAGGCCGATGGGGTGGATCTCCTGGGGTCAGGAATTCGAGACCAGTCTGGCCAACAT A G RAC1 Ensembl:ENSG00000136238 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs749667503 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_27639,RMVar_hsa_circ_114852,RMVar_hsa_circ_243626,RMVar_hsa_circ_77263,RMVar_hsa_circ_243625 48014 RMVar_ID_48014 Human_SNP_ID_308755109 A-to-I Human chr7 + 6382752 6382752 6382752 AAAATTAGCTGGATGTGGTGGTGCTTACGTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA AAAATTAGCTGGATGTGGTGGTGCTTACGTGTGGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA A G RAC1 Ensembl:ENSG00000136238 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1429214398 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_27639,RMVar_hsa_circ_114852,RMVar_hsa_circ_243626,RMVar_hsa_circ_77263,RMVar_hsa_circ_243625 48015 RMVar_ID_48015 Human_SNP_ID_308755864 A-to-I Human chr7 + 6384824 6384824 6384824 TTTTTTAATTTAAAAAAATTTATTTTTTTGAGACAGGGTCTCACTTTGTCCCTCAGACTGGATGC TTTTTTAATTTAAAAAAATTTATTTTTTTGAGGCAGGGTCTCACTTTGTCCCTCAGACTGGATGC A G RAC1 Ensembl:ENSG00000136238 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037383704 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16187845 RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_27639,RMVar_hsa_circ_114852,RMVar_hsa_circ_243626,RMVar_hsa_circ_77263,RMVar_hsa_circ_243625 48016 RMVar_ID_48016 Human_SNP_ID_308755898 A-to-I Human chr7 + 6384931 6384931 6384931 GGGTTCAAGTGATCCTCGTGCCTCAGCCCCCCAAGTAGCTGAGACTACTGCTGCACACCGCCACA GGGTTCAAGTGATCCTCGTGCCTCAGCCCCCCGAGTAGCTGAGACTACTGCTGCACACCGCCACA A G RAC1 Ensembl:ENSG00000136238 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs547738089 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16187851 Clinvar_Rec_132 RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_27639,RMVar_hsa_circ_114852,RMVar_hsa_circ_243626,RMVar_hsa_circ_77263,RMVar_hsa_circ_243625 48017 RMVar_ID_48017 Human_SNP_ID_308757139 A-to-I Human chr7 + 6388425 6388425 6388425 TGGAGTGCTGTGATGCGATCTCAGCTCACTGCAGCGTCTGCCTCCTGGGTTCAAGTGATTCTCTG TGGAGTGCTGTGATGCGATCTCAGCTCACTGCCGCGTCTGCCTCCTGGGTTCAAGTGATTCTCTG A C RAC1 Ensembl:ENSG00000136238 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs193093694 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2474910,Human_miRNA_ID_2960697,Human_miRNA_ID_2992772 RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_114852,RMVar_hsa_circ_243626,RMVar_hsa_circ_77263,RMVar_hsa_circ_243625,RMVar_hsa_circ_243627,RMVar_hsa_circ_243629,RMVar_hsa_circ_285328,RMVar_hsa_circ_333175,RMVar_hsa_circ_105571,RMVar_hsa_circ_243628 48018 RMVar_ID_48018 Human_SNP_ID_308757140 A-to-I Human chr7 + 6388425 6388425 6388425 TGGAGTGCTGTGATGCGATCTCAGCTCACTGCAGCGTCTGCCTCCTGGGTTCAAGTGATTCTCTG TGGAGTGCTGTGATGCGATCTCAGCTCACTGCTGCGTCTGCCTCCTGGGTTCAAGTGATTCTCTG A T RAC1 Ensembl:ENSG00000136238 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs193093694 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2474910,Human_miRNA_ID_2960697,Human_miRNA_ID_2992772 RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_114852,RMVar_hsa_circ_243626,RMVar_hsa_circ_77263,RMVar_hsa_circ_243625,RMVar_hsa_circ_243627,RMVar_hsa_circ_243629,RMVar_hsa_circ_285328,RMVar_hsa_circ_333175,RMVar_hsa_circ_105571,RMVar_hsa_circ_243628 48019 RMVar_ID_48019 Human_SNP_ID_308757595 A-to-I Human chr7 + 6389711 6389711 6389711 CCAAAAAAGAAAAAAAAAATATGTGTTTTTGTAGAGCTATGTTTTGCTATATTGCCCAGGCTGGT CCAAAAAAGAAAAAAAAAATATGTGTTTTTGTGGAGCTATGTTTTGCTATATTGCCCAGGCTGGT A G RAC1 Ensembl:ENSG00000136238 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1369820245 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_114852,RMVar_hsa_circ_243626,RMVar_hsa_circ_77263,RMVar_hsa_circ_243625,RMVar_hsa_circ_243627,RMVar_hsa_circ_243629,RMVar_hsa_circ_285328,RMVar_hsa_circ_333175,RMVar_hsa_circ_105571,RMVar_hsa_circ_243628 48020 RMVar_ID_48020 Human_SNP_ID_308757940 A-to-I Human chr7 + 6390398 6390398 6390398 CTGAGGTGGGCGCATTATGAGGTCAGGAGATCAAGACCAGCCTGATCAACATGGTGAAACCCCAT CTGAGGTGGGCGCATTATGAGGTCAGGAGATCGAGACCAGCCTGATCAACATGGTGAAACCCCAT A G RAC1 Ensembl:ENSG00000136238 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1314624768 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_114852,RMVar_hsa_circ_243626,RMVar_hsa_circ_77263,RMVar_hsa_circ_243625,RMVar_hsa_circ_243627,RMVar_hsa_circ_243629,RMVar_hsa_circ_285328,RMVar_hsa_circ_333175,RMVar_hsa_circ_105571,RMVar_hsa_circ_243628 48021 RMVar_ID_48021 Human_SNP_ID_308760076 A-to-I Human chr7 + 6396919 6396919 6396919 GGGCGTGGTGGCGGGCACCTGTGGTCCCAGCTACTCGGGAGGCTGAGGCAGGGAGAATGGTGTGA GGGCGTGGTGGCGGGCACCTGTGGTCCCAGCTGCTCGGGAGGCTGAGGCAGGGAGAATGGTGTGA A G RAC1 Ensembl:ENSG00000136238 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs888687121 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_174834 RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_114852,RMVar_hsa_circ_243626,RMVar_hsa_circ_243629,RMVar_hsa_circ_333175,RMVar_hsa_circ_105571,RMVar_hsa_circ_243628,RMVar_hsa_circ_126443,RMVar_hsa_circ_243631 48022 RMVar_ID_48022 Human_SNP_ID_308760301 A-to-I Human chr7 + 6397318 6397318 6397318 ATGAAATTAAAATAATTTTCTCATTTTGAGACAGGGTCTCGCTCTGTCACCCAGACTGGAGTGCA ATGAAATTAAAATAATTTTCTCATTTTGAGACGGGGTCTCGCTCTGTCACCCAGACTGGAGTGCA A G RAC1 Ensembl:ENSG00000136238 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1160639482 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_114852,RMVar_hsa_circ_243626,RMVar_hsa_circ_243629,RMVar_hsa_circ_333175,RMVar_hsa_circ_105571,RMVar_hsa_circ_243628,RMVar_hsa_circ_126443,RMVar_hsa_circ_243631 48023 RMVar_ID_48023 Human_SNP_ID_308765615 A-to-I Human chr7 - 6410816 6410816 6410816 CCTGTAAGCCGAGCTACTCAGTAGGCTGAGGTAGGAGAATCGCTTGAATTCGGGAGGCAGATTGT CCTGTAAGCCGAGCTACTCAGTAGGCTGAGGTGGGAGAATCGCTTGAATTCGGGAGGCAGATTGT T C DAGLB Ensembl:ENSG00000164535 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215666823 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6623 48024 RMVar_ID_48024 Human_SNP_ID_308767021 A-to-I Human chr7 - 6414405 6414405 6414405 GGGAGGCTGAGGCAGTAGGATTGCCTGAACCCAGGATGAAGAGGTTGCCGTGAGCCGAGATCGTG GGGAGGCTGAGGCAGTAGGATTGCCTGAACCCCGGATGAAGAGGTTGCCGTGAGCCGAGATCGTG T G DAGLB Ensembl:ENSG00000164535 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs969147981 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_243639,RMVar_hsa_circ_266979,RMVar_hsa_circ_335627,RMVar_hsa_circ_344890,RMVar_hsa_circ_377030,RMVar_hsa_circ_282450,RMVar_hsa_circ_41686,RMVar_hsa_circ_266220,RMVar_hsa_circ_268538 48025 RMVar_ID_48025 Human_SNP_ID_308767029 A-to-I Human chr7 - 6414424 6414424 6414424 CCTGTGGTCCCAGCTACCCGGGAGGCTGAGGCAGTAGGATTGCCTGAACCCAGGATGAAGAGGTT CCTGTGGTCCCAGCTACCCGGGAGGCTGAGGCGGTAGGATTGCCTGAACCCAGGATGAAGAGGTT T C DAGLB Ensembl:ENSG00000164535 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs959233494 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16190056 RMVar_hsa_circ_243639,RMVar_hsa_circ_266979,RMVar_hsa_circ_335627,RMVar_hsa_circ_344890,RMVar_hsa_circ_377030,RMVar_hsa_circ_282450,RMVar_hsa_circ_41686,RMVar_hsa_circ_266220,RMVar_hsa_circ_268538 48026 RMVar_ID_48026 Human_SNP_ID_308768122 A-to-I Human chr7 - 6417262 6417260 6417262 CGCCACCAAGCCCCGTTAATTTTTTTTTTTTTAGTAGAGTCAGGATCCAGGCTGGTCTTGTATTT CGCCACCAAGCCCCGTTAATTTTTTTTTTTTT__TAGAGTCAGGATCCAGGCTGGTCTTGTATTT ACT A DAGLB Ensembl:ENSG00000164535 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1447709597 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_335627,RMVar_hsa_circ_344890,RMVar_hsa_circ_377030,RMVar_hsa_circ_41686,RMVar_hsa_circ_268538,RMVar_hsa_circ_323958,RMVar_hsa_circ_346908,RMVar_hsa_circ_243641,RMVar_hsa_circ_243642,RMVar_hsa_circ_113623 48027 RMVar_ID_48027 Human_SNP_ID_308768128 A-to-I Human chr7 - 6417262 6417262 6417262 CGCCACCAAGCCCCGTTAATTTTTTTTTTTTTAGTAGAGTCAGGATCCAGGCTGGTCTTGTATTT CGCCACCAAGCCCCGTTAATTTTTTTTTTTTTTGTAGAGTCAGGATCCAGGCTGGTCTTGTATTT T A DAGLB Ensembl:ENSG00000164535 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965102935 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_335627,RMVar_hsa_circ_344890,RMVar_hsa_circ_377030,RMVar_hsa_circ_41686,RMVar_hsa_circ_268538,RMVar_hsa_circ_323958,RMVar_hsa_circ_346908,RMVar_hsa_circ_243641,RMVar_hsa_circ_243642,RMVar_hsa_circ_113623 48028 RMVar_ID_48028 Human_SNP_ID_308768129 A-to-I Human chr7 - 6417262 6417262 6417262 CGCCACCAAGCCCCGTTAATTTTTTTTTTTTTAGTAGAGTCAGGATCCAGGCTGGTCTTGTATTT CGCCACCAAGCCCCGTTAATTTTTTTTTTTTTGGTAGAGTCAGGATCCAGGCTGGTCTTGTATTT T C DAGLB Ensembl:ENSG00000164535 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965102935 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_335627,RMVar_hsa_circ_344890,RMVar_hsa_circ_377030,RMVar_hsa_circ_41686,RMVar_hsa_circ_268538,RMVar_hsa_circ_323958,RMVar_hsa_circ_346908,RMVar_hsa_circ_243641,RMVar_hsa_circ_243642,RMVar_hsa_circ_113623 48029 RMVar_ID_48029 Human_SNP_ID_308768294 A-to-I Human chr7 - 6417696 6417696 6417696 CTGTAGTTGTTTTAGAGAAATGGGGTCTTGCTATGTGGCCCAGGCTGGTCTCAACCTCATGCGTT CTGTAGTTGTTTTAGAGAAATGGGGTCTTGCTGTGTGGCCCAGGCTGGTCTCAACCTCATGCGTT T C DAGLB Ensembl:ENSG00000164535 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1050267794 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_335627,RMVar_hsa_circ_344890,RMVar_hsa_circ_377030,RMVar_hsa_circ_41686,RMVar_hsa_circ_268538,RMVar_hsa_circ_323958,RMVar_hsa_circ_346908,RMVar_hsa_circ_243641,RMVar_hsa_circ_243642,RMVar_hsa_circ_113623 48030 RMVar_ID_48030 Human_SNP_ID_308768295 A-to-I Human chr7 - 6417696 6417696 6417696 CTGTAGTTGTTTTAGAGAAATGGGGTCTTGCTATGTGGCCCAGGCTGGTCTCAACCTCATGCGTT CTGTAGTTGTTTTAGAGAAATGGGGTCTTGCTCTGTGGCCCAGGCTGGTCTCAACCTCATGCGTT T G DAGLB Ensembl:ENSG00000164535 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1050267794 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_335627,RMVar_hsa_circ_344890,RMVar_hsa_circ_377030,RMVar_hsa_circ_41686,RMVar_hsa_circ_268538,RMVar_hsa_circ_323958,RMVar_hsa_circ_346908,RMVar_hsa_circ_243641,RMVar_hsa_circ_243642,RMVar_hsa_circ_113623 48031 RMVar_ID_48031 Human_SNP_ID_308768472 A-to-I Human chr7 - 6418286 6418286 6418286 TAGTTCACTGTAACCTTGAACTCCTGGGCTCAAGTGATCCTCCTGCCTCAGCCTCCCAAAGTGTT TAGTTCACTGTAACCTTGAACTCCTGGGCTCAGGTGATCCTCCTGCCTCAGCCTCCCAAAGTGTT T C DAGLB Ensembl:ENSG00000164535 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs575940116 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_335627,RMVar_hsa_circ_344890,RMVar_hsa_circ_377030,RMVar_hsa_circ_41686,RMVar_hsa_circ_268538,RMVar_hsa_circ_323958,RMVar_hsa_circ_346908,RMVar_hsa_circ_243641,RMVar_hsa_circ_243642,RMVar_hsa_circ_113623 48032 RMVar_ID_48032 Human_SNP_ID_308770346 A-to-I Human chr7 - 6423103 6423103 6423103 GGAATACAGGCATGTGCCACTACACCCAGCTAATTTTTTCTATTTTTGTAGAGACAGGATCTCAC GGAATACAGGCATGTGCCACTACACCCAGCTAGTTTTTTCTATTTTTGTAGAGACAGGATCTCAC T C DAGLB Ensembl:ENSG00000164535 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947747375 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_243643,RMVar_hsa_circ_335627,RMVar_hsa_circ_344890,RMVar_hsa_circ_41686,RMVar_hsa_circ_346908,RMVar_hsa_circ_243647,RMVar_hsa_circ_292178,RMVar_hsa_circ_243642,RMVar_hsa_circ_113623,RMVar_hsa_circ_326242,RMVar_hsa_circ_341518,RMVar_hsa_circ_378912,RMVar_hsa_circ_317378,RMVar_hsa_circ_284042,RMVar_hsa_circ_243648,RMVar_hsa_circ_243645,RMVar_hsa_circ_243646,RMVar_hsa_circ_243644 48033 RMVar_ID_48033 Human_SNP_ID_308771765 A-to-I Human chr7 - 6427008 6427008 6427008 TGCCTCCCAGTTGCAAGCAAGTCTCCTGCCTCAGCGTCCCGAGTAGCTGGGATTACAGGCGCCTG TGCCTCCCAGTTGCAAGCAAGTCTCCTGCCTCGGCGTCCCGAGTAGCTGGGATTACAGGCGCCTG T C DAGLB Ensembl:ENSG00000164535 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1266894799 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_243643,RMVar_hsa_circ_41686,RMVar_hsa_circ_292178,RMVar_hsa_circ_243642,RMVar_hsa_circ_113623,RMVar_hsa_circ_326242,RMVar_hsa_circ_341518,RMVar_hsa_circ_378912,RMVar_hsa_circ_243645,RMVar_hsa_circ_243646,RMVar_hsa_circ_243644,RMVar_hsa_circ_243653,RMVar_hsa_circ_270337,RMVar_hsa_circ_243651,RMVar_hsa_circ_339141,RMVar_hsa_circ_346174,RMVar_hsa_circ_322513,RMVar_hsa_circ_69532,RMVar_hsa_circ_282732,RMVar_hsa_circ_285485,RMVar_hsa_circ_280272,RMVar_hsa_circ_243655,RMVar_hsa_circ_243656,RMVar_hsa_circ_243654 48034 RMVar_ID_48034 Human_SNP_ID_308772259 A-to-I Human chr7 - 6428563 6428563 6428563 AGAATCGCTTGAACCAGGGAGTTGGAGGTTGCAGTGAGTGGAGATCACACCATTGCCCTGCAGCC AGAATCGCTTGAACCAGGGAGTTGGAGGTTGCTGTGAGTGGAGATCACACCATTGCCCTGCAGCC T A DAGLB Ensembl:ENSG00000164535 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs536533884 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_243643,RMVar_hsa_circ_41686,RMVar_hsa_circ_292178,RMVar_hsa_circ_243642,RMVar_hsa_circ_113623,RMVar_hsa_circ_326242,RMVar_hsa_circ_341518,RMVar_hsa_circ_378912,RMVar_hsa_circ_243645,RMVar_hsa_circ_243646,RMVar_hsa_circ_243644,RMVar_hsa_circ_243653,RMVar_hsa_circ_270337,RMVar_hsa_circ_243651,RMVar_hsa_circ_339141,RMVar_hsa_circ_346174,RMVar_hsa_circ_322513,RMVar_hsa_circ_69532,RMVar_hsa_circ_282732,RMVar_hsa_circ_285485,RMVar_hsa_circ_280272,RMVar_hsa_circ_243655,RMVar_hsa_circ_243656,RMVar_hsa_circ_243654 48035 RMVar_ID_48035 Human_SNP_ID_308772416 A-to-I Human chr7 - 6429077 6429077 6429077 GTCCCAGGCCGGGCGTGGTGGCTCAGACCTGTAATCCCAGCATTTTGGGAGGTCGAGGCCAGCGG GTCCCAGGCCGGGCGTGGTGGCTCAGACCTGTGATCCCAGCATTTTGGGAGGTCGAGGCCAGCGG T C DAGLB Ensembl:ENSG00000164535 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs761071548 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_243643,RMVar_hsa_circ_41686,RMVar_hsa_circ_292178,RMVar_hsa_circ_243642,RMVar_hsa_circ_113623,RMVar_hsa_circ_326242,RMVar_hsa_circ_341518,RMVar_hsa_circ_378912,RMVar_hsa_circ_243645,RMVar_hsa_circ_243646,RMVar_hsa_circ_243644,RMVar_hsa_circ_243653,RMVar_hsa_circ_270337,RMVar_hsa_circ_243651,RMVar_hsa_circ_339141,RMVar_hsa_circ_346174,RMVar_hsa_circ_322513,RMVar_hsa_circ_69532,RMVar_hsa_circ_282732,RMVar_hsa_circ_285485,RMVar_hsa_circ_280272,RMVar_hsa_circ_243655,RMVar_hsa_circ_243656,RMVar_hsa_circ_243654 48036 RMVar_ID_48036 Human_SNP_ID_308784678 A-to-I Human chr7 - 6463520 6463520 6463520 ACTTTTTTTGCCCAGGCTGGTCTTGAACTCCTAGCTTCAAGGGATCCTCCCACCCTGGCCTGCCA ACTTTTTTTGCCCAGGCTGGTCTTGAACTCCTGGCTTCAAGGGATCCTCCCACCCTGGCCTGCCA T C KDELR2,DAGLB Ensembl:ENSG00000136240,Ensembl:ENSG00000164535 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs954425976 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2142061,Human_miRNA_ID_3045867 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 48037 RMVar_ID_48037 Human_SNP_ID_308784993 A-to-I Human chr7 - 6464273 6464273 6464273 CTCGTGATCCGCACACCTCAGCCTCCCAAAGTATTGGGATTACAGGCGTGAGCCACCACGCCTAG CTCGTGATCCGCACACCTCAGCCTCCCAAAGTTTTGGGATTACAGGCGTGAGCCACCACGCCTAG T A KDELR2,DAGLB Ensembl:ENSG00000136240,Ensembl:ENSG00000164535 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1269966756 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2418217 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 48038 RMVar_ID_48038 Human_SNP_ID_308784994 A-to-I Human chr7 - 6464273 6464273 6464273 CTCGTGATCCGCACACCTCAGCCTCCCAAAGTATTGGGATTACAGGCGTGAGCCACCACGCCTAG CTCGTGATCCGCACACCTCAGCCTCCCAAAGTGTTGGGATTACAGGCGTGAGCCACCACGCCTAG T C KDELR2,DAGLB Ensembl:ENSG00000136240,Ensembl:ENSG00000164535 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1269966756 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2418217 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 48039 RMVar_ID_48039 Human_SNP_ID_308785008 A-to-I Human chr7 - 6464307 6464307 6464307 ACCTTGTTGGCCAGGCTGGTCTTGAACTCCCAACCTCGTGATCCGCACACCTCAGCCTCCCAAAG ACCTTGTTGGCCAGGCTGGTCTTGAACTCCCAGCCTCGTGATCCGCACACCTCAGCCTCCCAAAG T C KDELR2,DAGLB Ensembl:ENSG00000136240,Ensembl:ENSG00000164535 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1424647421 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2076973 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 48040 RMVar_ID_48040 Human_SNP_ID_308785027 A-to-I Human chr7 - 6464355 6464355 6464355 ACCACCACGCCCGGCTAATTTTTGTATTTTTAATAGAGACGGGGTTTCACCTTGTTGGCCAGGCT ACCACCACGCCCGGCTAATTTTTGTATTTTTATTAGAGACGGGGTTTCACCTTGTTGGCCAGGCT T A KDELR2,DAGLB Ensembl:ENSG00000136240,Ensembl:ENSG00000164535 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs921313791 Functional Loss SNV dbSNP153 33..33 33 - - - 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 48041 RMVar_ID_48041 Human_SNP_ID_308785028 A-to-I Human chr7 - 6464355 6464355 6464355 ACCACCACGCCCGGCTAATTTTTGTATTTTTAATAGAGACGGGGTTTCACCTTGTTGGCCAGGCT ACCACCACGCCCGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCTTGTTGGCCAGGCT T C KDELR2,DAGLB Ensembl:ENSG00000136240,Ensembl:ENSG00000164535 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs921313791 Functional Loss SNV dbSNP153 33..33 33 - - - 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 48042 RMVar_ID_48042 Human_SNP_ID_308785029 A-to-I Human chr7 - 6464362 6464362 6464362 GGTGCGCACCACCACGCCCGGCTAATTTTTGTATTTTTAATAGAGACGGGGTTTCACCTTGTTGG GGTGCGCACCACCACGCCCGGCTAATTTTTGTGTTTTTAATAGAGACGGGGTTTCACCTTGTTGG T C KDELR2,DAGLB Ensembl:ENSG00000136240,Ensembl:ENSG00000164535 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1268449630 Functional Loss SNV dbSNP153 33..33 33 - - - 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 48043 RMVar_ID_48043 Human_SNP_ID_308785366 A-to-I Human chr7 - 6465312 6465308 6465312 AGGCGTGGTGGTGGGCGCCTGTAGTCCCAGTTACTCGGGAGGCTGAGGCAGGAGAATGGTGTGAA AGGCGTGGTGGTGGGCGCCTGTAGTCCCAGTT____GGGAGGCTGAGGCAGGAGAATGGTGTGAA CGAGT C KDELR2,DAGLB Ensembl:ENSG00000136240,Ensembl:ENSG00000164535 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1223860030 Functional Loss DEL dbSNP153 33..36 33 - - - 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 48044 RMVar_ID_48044 Human_SNP_ID_308785372 A-to-I Human chr7 - 6465312 6465312 6465312 AGGCGTGGTGGTGGGCGCCTGTAGTCCCAGTTACTCGGGAGGCTGAGGCAGGAGAATGGTGTGAA AGGCGTGGTGGTGGGCGCCTGTAGTCCCAGTTGCTCGGGAGGCTGAGGCAGGAGAATGGTGTGAA T C KDELR2,DAGLB Ensembl:ENSG00000136240,Ensembl:ENSG00000164535 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1012905062 Functional Loss SNV dbSNP153 33..33 33 - - - 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 48045 RMVar_ID_48045 Human_SNP_ID_308787151 A-to-I Human chr7 - 6470733 6470733 6470733 TCCGTGCATGATGGTGGTCATAGTGGTGGCGGATTAAATCAAGAAGTATATGTTTACAAACAAAA TCCGTGCATGATGGTGGTCATAGTGGTGGCGGGTTAAATCAAGAAGTATATGTTTACAAACAAAA T C KDELR2,DAGLB Ensembl:ENSG00000136240,Ensembl:ENSG00000164535 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs58885063 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3097202,Human_RBP_ID_16191821,Human_RBP_ID_17577103 Human_miRNA_ID_2343729 RMVar_hsa_circ_91785,RMVar_hsa_circ_243659,RMVar_hsa_circ_120377,RMVar_hsa_circ_243668,RMVar_hsa_circ_316068,RMVar_hsa_circ_271617,RMVar_hsa_circ_243672 48046 RMVar_ID_48046 Human_SNP_ID_308787428 A-to-I Human chr7 - 6471452 6471452 6471452 AAACAGGCCGGGTGCTGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAAGCCGAGGCAGGCAGA AAACAGGCCGGGTGCTGTGGCTCACGCCTGTATTCCCAGCACTTTGGGAAGCCGAGGCAGGCAGA T A KDELR2,DAGLB Ensembl:ENSG00000136240,Ensembl:ENSG00000164535 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1384941637 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91785,RMVar_hsa_circ_243659,RMVar_hsa_circ_120377,RMVar_hsa_circ_243668,RMVar_hsa_circ_316068,RMVar_hsa_circ_271617,RMVar_hsa_circ_243672 48047 RMVar_ID_48047 Human_SNP_ID_308788574 A-to-I Human chr7 - 6475315 6475315 6475315 TCACGCAATCCTCCCACCTCAACCTCCCATGTAGCTGGGACCACAGGTGTGTGCCACCTTGCCTG TCACGCAATCCTCCCACCTCAACCTCCCATGTCGCTGGGACCACAGGTGTGTGCCACCTTGCCTG T G KDELR2,DAGLB Ensembl:ENSG00000136240,Ensembl:ENSG00000164535 Protein coding,Protein coding intron,intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs551310233 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26138494 RMVar_hsa_circ_91785,RMVar_hsa_circ_243659 48048 RMVar_ID_48048 Human_SNP_ID_308790141 A-to-I Human chr7 - 6481186 6481186 6481186 TTTTGTATTTTTAGTAGAGACAGAGTTTCACCATGTTGGCCAGGCTGGTCTCGGTCTCCTGACCT TTTTGTATTTTTAGTAGAGACAGAGTTTCACCGTGTTGGCCAGGCTGGTCTCGGTCTCCTGACCT T C KDELR2,DAGLB Ensembl:ENSG00000136240,Ensembl:ENSG00000164535 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1245704289 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91785,RMVar_hsa_circ_243659 48049 RMVar_ID_48049 Human_SNP_ID_308790142 A-to-I Human chr7 - 6481186 6481186 6481186 TTTTGTATTTTTAGTAGAGACAGAGTTTCACCATGTTGGCCAGGCTGGTCTCGGTCTCCTGACCT TTTTGTATTTTTAGTAGAGACAGAGTTTCACCCTGTTGGCCAGGCTGGTCTCGGTCTCCTGACCT T G KDELR2,DAGLB Ensembl:ENSG00000136240,Ensembl:ENSG00000164535 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1245704289 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91785,RMVar_hsa_circ_243659 48050 RMVar_ID_48050 Human_SNP_ID_308790300 A-to-I Human chr7 - 6481660 6481660 6481660 GCTGGAGTGCAATGGCTGTGTCACGGCTCACTACAGCCCCAAACTCCTGGGCTCAAGCGATCCTC GCTGGAGTGCAATGGCTGTGTCACGGCTCACTGCAGCCCCAAACTCCTGGGCTCAAGCGATCCTC T C KDELR2,DAGLB Ensembl:ENSG00000136240,Ensembl:ENSG00000164535 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs993892493 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2992776 RMVar_hsa_circ_91785,RMVar_hsa_circ_243659 48051 RMVar_ID_48051 Human_SNP_ID_308790306 A-to-I Human chr7 - 6481681 6481681 6481681 ATGTCTCACTCTGTCCCCCAGGCTGGAGTGCAATGGCTGTGTCACGGCTCACTACAGCCCCAAAC ATGTCTCACTCTGTCCCCCAGGCTGGAGTGCAGTGGCTGTGTCACGGCTCACTACAGCCCCAAAC T C KDELR2,DAGLB Ensembl:ENSG00000136240,Ensembl:ENSG00000164535 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459117563 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16192286 RMVar_hsa_circ_91785,RMVar_hsa_circ_243659 48052 RMVar_ID_48052 Human_SNP_ID_308821425 A-to-I Human chr7 + 6580235 6580235 6580235 GTTGCCCAGGCTGGTCTCGAACTCCTGAGCTCAAGCGATCCACCCACCTCTGCTTCCCAGAGTGC GTTGCCCAGGCTGGTCTCGAACTCCTGAGCTCTAGCGATCCACCCACCTCTGCTTCCCAGAGTGC A T ZDHHC4 Ensembl:ENSG00000136247 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1333724369 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_79051,RMVar_hsa_circ_96510,RMVar_hsa_circ_86701,RMVar_hsa_circ_353357,RMVar_hsa_circ_243677,RMVar_hsa_circ_307301,RMVar_hsa_circ_243679,RMVar_hsa_circ_243680,RMVar_hsa_circ_333529,RMVar_hsa_circ_243678,RMVar_hsa_circ_271401,RMVar_hsa_circ_243681,RMVar_hsa_circ_243682 48053 RMVar_ID_48053 Human_SNP_ID_308822421 A-to-I Human chr7 + 6583377 6583377 6583377 TTTATGAATTTGATGAAGTGATGTTTCCAAAGAACGTGAGGTGCTCTACTTGTGATTTAAGGAAA TTTATGAATTTGATGAAGTGATGTTTCCAAAGGACGTGAGGTGCTCTACTTGTGATTTAAGGAAA A G ZDHHC4 Ensembl:ENSG00000136247 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs373744322 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_687319,Human_RBP_ID_2045536,Human_RBP_ID_18108776,Human_RBP_ID_24222195 Human_Splice_Rec_842326,Human_Splice_Rec_842327,Human_Splice_Rec_842340,Human_Splice_Rec_842341,Human_Splice_Rec_842356,Human_Splice_Rec_842357,Human_Splice_Rec_842370,Human_Splice_Rec_842371,Human_Splice_Rec_842396,Human_Splice_Rec_842406,Human_Splice_Rec_842407,Human_Splice_Rec_842422,Human_Splice_Rec_842438,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 48054 RMVar_ID_48054 Human_SNP_ID_308825483 A-to-I Human chr7 + 6592288 6592288 6592288 TTGTTTGTTTGTTTAAATTATTTTTTTTGGCCATGCTTAGTGGTTCACTCCTGTAATCCCAGCAC TTGTTTGTTTGTTTAAATTATTTTTTTTGGCCCTGCTTAGTGGTTCACTCCTGTAATCCCAGCAC A C C7orf26 Ensembl:ENSG00000146576 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1027477033 Functional Loss SNV dbSNP153 33..33 33 - - - 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_243694 48055 RMVar_ID_48055 Human_SNP_ID_308825484 A-to-I Human chr7 + 6592288 6592288 6592288 TTGTTTGTTTGTTTAAATTATTTTTTTTGGCCATGCTTAGTGGTTCACTCCTGTAATCCCAGCAC TTGTTTGTTTGTTTAAATTATTTTTTTTGGCCGTGCTTAGTGGTTCACTCCTGTAATCCCAGCAC A G C7orf26 Ensembl:ENSG00000146576 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1027477033 Functional Loss SNV dbSNP153 33..33 33 - - - 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_243694 48056 RMVar_ID_48056 Human_SNP_ID_308825657 A-to-I Human chr7 + 6592721 6592721 6592721 GCCTTTGCCTCCTGGGCTCAAGTGATCCTCCTACCTCAGCCCTCCAAGTAGCTGGGACCACAGGC GCCTTTGCCTCCTGGGCTCAAGTGATCCTCCTCCCTCAGCCCTCCAAGTAGCTGGGACCACAGGC A C C7orf26 Ensembl:ENSG00000146576 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1369462855 Functional Loss SNV dbSNP153 33..33 33 - - - 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_243694 48057 RMVar_ID_48057 Human_SNP_ID_308827586 A-to-I Human chr7 + 6598217 6598217 6598217 CGTGGCCGGGACGGGTGGCTCACTCCTGTAATACCAGCACTTTGGGAGGCCGAGGTGGGCGGATC CGTGGCCGGGACGGGTGGCTCACTCCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGCGGATC A C C7orf26 Ensembl:ENSG00000146576 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs536222483 Functional Loss SNV dbSNP153 33..33 33 - - - 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 48058 RMVar_ID_48058 Human_SNP_ID_308827590 A-to-I Human chr7 + 6598223 6598223 6598223 CGGGACGGGTGGCTCACTCCTGTAATACCAGCACTTTGGGAGGCCGAGGTGGGCGGATCACCTGC CGGGACGGGTGGCTCACTCCTGTAATACCAGCGCTTTGGGAGGCCGAGGTGGGCGGATCACCTGC A G C7orf26 Ensembl:ENSG00000146576 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1302436589 Functional Loss SNV dbSNP153 33..33 33 - - - 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 48059 RMVar_ID_48059 Human_SNP_ID_308829779 A-to-I Human chr7 + 6604216 6604216 6604216 CTCCCACCTCAGCCTCCCAAGTAGCTGGGACTACAGGTGTGCGCCACCACAGCAGGCTGATTTTT CTCCCACCTCAGCCTCCCAAGTAGCTGGGACTGCAGGTGTGCGCCACCACAGCAGGCTGATTTTT A G C7orf26 Ensembl:ENSG00000146576 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs539869830 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_110083,RMVar_hsa_circ_243694 48060 RMVar_ID_48060 Human_SNP_ID_308830601 A-to-I Human chr7 + 6606845 6606845 6606845 CTCCTGCCCCAGCCTCCTGAGTAGCTGGGACTAAAGGTGTGCACCACCACGCCCAGCTAATTTTT CTCCTGCCCCAGCCTCCTGAGTAGCTGGGACTGAAGGTGTGCACCACCACGCCCAGCTAATTTTT A G C7orf26 Ensembl:ENSG00000146576 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1337113238 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_110083,RMVar_hsa_circ_243694 48061 RMVar_ID_48061 Human_SNP_ID_308830616 A-to-I Human chr7 + 6606898 6606898 6606898 CAGCTAATTTTTAGTTTATTTTCTGTGGAGATAGGGTCTCACTGTATTGCTCCGTCTGGTCTTGA CAGCTAATTTTTAGTTTATTTTCTGTGGAGATGGGGTCTCACTGTATTGCTCCGTCTGGTCTTGA A G C7orf26 Ensembl:ENSG00000146576 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1457094257 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102217,RMVar_hsa_circ_243469,RMVar_hsa_circ_110083,RMVar_hsa_circ_243694 48062 RMVar_ID_48062 Human_SNP_ID_308860980 A-to-I Human chr7 - 6701070 6701070 6701070 GGAAGGCTGAGGCAGAAGCATCACTTGAGCCCAGGAATATGAGGCTGCAGTGAGCTATGATTGCA GGAAGGCTGAGGCAGAAGCATCACTTGAGCCCGGGAATATGAGGCTGCAGTGAGCTATGATTGCA T C ZNF12 Ensembl:ENSG00000164631 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs994617037 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27304,RMVar_hsa_circ_243709,RMVar_hsa_circ_291734 48063 RMVar_ID_48063 Human_SNP_ID_308860994 A-to-I Human chr7 - 6701122 6701122 6701122 AAATGCATCCTCAGCCGGGCATAGTGGCTCACACCAGTAATCCCAACACTTTGGAAGGCTGAGGC AAATGCATCCTCAGCCGGGCATAGTGGCTCACGCCAGTAATCCCAACACTTTGGAAGGCTGAGGC T C ZNF12 Ensembl:ENSG00000164631 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs778594907 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16200934,Human_RBP_ID_24222717 RMVar_hsa_circ_27304,RMVar_hsa_circ_243709,RMVar_hsa_circ_291734 48064 RMVar_ID_48064 Human_SNP_ID_308861001 A-to-I Human chr7 - 6701134 6701134 6701134 AAGTCTGATTTTAAATGCATCCTCAGCCGGGCATAGTGGCTCACACCAGTAATCCCAACACTTTG AAGTCTGATTTTAAATGCATCCTCAGCCGGGCTTAGTGGCTCACACCAGTAATCCCAACACTTTG T A ZNF12 Ensembl:ENSG00000164631 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1216088804 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27304,RMVar_hsa_circ_243709,RMVar_hsa_circ_291734 48065 RMVar_ID_48065 Human_SNP_ID_308874831 A-to-I Human chr7 + 6747535 6747535 6747535 GAGTTCAGGAGATCGAGACCATCCTGGCTAACATGGTGAAAGCCCGTCTCTACTAAAAATACAAA GAGTTCAGGAGATCGAGACCATCCTGGCTAACGTGGTGAAAGCCCGTCTCTACTAAAAATACAAA A G PMS2CL Ensembl:ENSG00000187953 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs867139250 Functional Loss SNV dbSNP153 33..33 33 - - - 48066 RMVar_ID_48066 Human_SNP_ID_308885113 A-to-I Human chr7 - 6799063 6799063 6799063 ATTTCGACTCGGTCTGCTGATCTGAGGTTTTTAGATTTTAAATATTTATGTGGAATTAATTAAAG ATTTCGACTCGGTCTGCTGATCTGAGGTTTTTCGATTTTAAATATTTATGTGGAATTAATTAAAG T G CCZ1B Ensembl:ENSG00000146574 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs552703424 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265391 48067 RMVar_ID_48067 Human_SNP_ID_308890095 A-to-I Human chr7 - 6817045 6817045 6817045 AAAACAGCCTCTTACTCCAGGCGCCAACGCTTACACCTGTCATCCCAGCACTTTGGGAGGCTGAG AAAACAGCCTCTTACTCCAGGCGCCAACGCTTCCACCTGTCATCCCAGCACTTTGGGAGGCTGAG T G CCZ1B Ensembl:ENSG00000146574 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1487787904 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5578,RMVar_hsa_circ_43721,RMVar_hsa_circ_265391,RMVar_hsa_circ_332358,RMVar_hsa_circ_311232,RMVar_hsa_circ_373049,RMVar_hsa_circ_318992,RMVar_hsa_circ_346528,RMVar_hsa_circ_322701,RMVar_hsa_circ_243720,RMVar_hsa_circ_243721,RMVar_hsa_circ_264885,RMVar_hsa_circ_329315,RMVar_hsa_circ_337704,RMVar_hsa_circ_309347,RMVar_hsa_circ_315962,RMVar_hsa_circ_243724,RMVar_hsa_circ_276807,RMVar_hsa_circ_8671,RMVar_hsa_circ_305546,RMVar_hsa_circ_356751,RMVar_hsa_circ_283230,RMVar_hsa_circ_243722,RMVar_hsa_circ_243723,RMVar_hsa_circ_285500,RMVar_hsa_circ_309234,RMVar_hsa_circ_368436,RMVar_hsa_circ_279360,RMVar_hsa_circ_243726,RMVar_hsa_circ_243727,RMVar_hsa_circ_243725 48068 RMVar_ID_48068 Human_SNP_ID_308892232 A-to-I Human chr7 - 6822899 6822899 6822899 GAATTCAGGACCAGTCTGGGCAATATAGCAAGACCCCATCTCTACAAAAAAATTTTATAAAAGTT GAATTCAGGACCAGTCTGGGCAATATAGCAAGGCCCCATCTCTACAAAAAAATTTTATAAAAGTT T C CCZ1B Ensembl:ENSG00000146574 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1268220465 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18103264 RMVar_hsa_circ_5578,RMVar_hsa_circ_43721,RMVar_hsa_circ_311232,RMVar_hsa_circ_346528,RMVar_hsa_circ_322701,RMVar_hsa_circ_243721,RMVar_hsa_circ_264885,RMVar_hsa_circ_315962,RMVar_hsa_circ_305546,RMVar_hsa_circ_356751,RMVar_hsa_circ_243723,RMVar_hsa_circ_309234,RMVar_hsa_circ_368436,RMVar_hsa_circ_279360,RMVar_hsa_circ_243726,RMVar_hsa_circ_243727,RMVar_hsa_circ_283805,RMVar_hsa_circ_321359,RMVar_hsa_circ_243729,RMVar_hsa_circ_243730,RMVar_hsa_circ_116069,RMVar_hsa_circ_357798 48069 RMVar_ID_48069 Human_SNP_ID_308892234 A-to-I Human chr7 - 6822905 6822905 6822905 GCCCAGGAATTCAGGACCAGTCTGGGCAATATAGCAAGACCCCATCTCTACAAAAAAATTTTATA GCCCAGGAATTCAGGACCAGTCTGGGCAATATGGCAAGACCCCATCTCTACAAAAAAATTTTATA T C CCZ1B Ensembl:ENSG00000146574 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs939534266 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5578,RMVar_hsa_circ_43721,RMVar_hsa_circ_311232,RMVar_hsa_circ_346528,RMVar_hsa_circ_322701,RMVar_hsa_circ_243721,RMVar_hsa_circ_264885,RMVar_hsa_circ_315962,RMVar_hsa_circ_305546,RMVar_hsa_circ_356751,RMVar_hsa_circ_243723,RMVar_hsa_circ_309234,RMVar_hsa_circ_368436,RMVar_hsa_circ_279360,RMVar_hsa_circ_243726,RMVar_hsa_circ_243727,RMVar_hsa_circ_283805,RMVar_hsa_circ_321359,RMVar_hsa_circ_243729,RMVar_hsa_circ_243730,RMVar_hsa_circ_116069,RMVar_hsa_circ_357798 48070 RMVar_ID_48070 Human_SNP_ID_309062961 A-to-I Human chr7 - 7357486 7357486 7357486 CCCAGCTAATTTTTGTATTCTTAGCAGAGACAAAGTTTCACCATGTTGGTCAGGCTGGTCACGAA CCCAGCTAATTTTTGTATTCTTAGCAGAGACACAGTTTCACCATGTTGGTCAGGCTGGTCACGAA T G COL28A1 Ensembl:ENSG00000215018 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs541733097 Functional Loss SNV dbSNP153 33..33 33 - - - 48071 RMVar_ID_48071 Human_SNP_ID_309128867 A-to-I Human chr7 + 7594326 7594325 7594326 TTTGGTGTGCATTTGGACTTTTTTTTTTTTTTAAATGGAGTCTCATTCTGTCACCCAGACTACAG TTTGGTGTGCATTTGGACTTTTTTTTTTTTTT_AATGGAGTCTCATTCTGTCACCCAGACTACAG TA T MIOS Ensembl:ENSG00000164654 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1259996148 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_760,RMVar_hsa_circ_359194,RMVar_hsa_circ_243742,RMVar_hsa_circ_266575,RMVar_hsa_circ_285661,RMVar_hsa_circ_72839,RMVar_hsa_circ_95013,RMVar_hsa_circ_243744,RMVar_hsa_circ_243745 48072 RMVar_ID_48072 Human_SNP_ID_309128868 A-to-I Human chr7 + 7594326 7594326 7594326 TTTGGTGTGCATTTGGACTTTTTTTTTTTTTTAAATGGAGTCTCATTCTGTCACCCAGACTACAG TTTGGTGTGCATTTGGACTTTTTTTTTTTTTTGAATGGAGTCTCATTCTGTCACCCAGACTACAG A G MIOS Ensembl:ENSG00000164654 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934091264 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_760,RMVar_hsa_circ_359194,RMVar_hsa_circ_243742,RMVar_hsa_circ_266575,RMVar_hsa_circ_285661,RMVar_hsa_circ_72839,RMVar_hsa_circ_95013,RMVar_hsa_circ_243744,RMVar_hsa_circ_243745 48073 RMVar_ID_48073 Human_SNP_ID_309128869 A-to-I Human chr7 + 7594326 7594326 7594326 TTTGGTGTGCATTTGGACTTTTTTTTTTTTTTAAATGGAGTCTCATTCTGTCACCCAGACTACAG TTTGGTGTGCATTTGGACTTTTTTTTTTTTTTTAATGGAGTCTCATTCTGTCACCCAGACTACAG A T MIOS Ensembl:ENSG00000164654 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934091264 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_760,RMVar_hsa_circ_359194,RMVar_hsa_circ_243742,RMVar_hsa_circ_266575,RMVar_hsa_circ_285661,RMVar_hsa_circ_72839,RMVar_hsa_circ_95013,RMVar_hsa_circ_243744,RMVar_hsa_circ_243745 48074 RMVar_ID_48074 Human_SNP_ID_309128882 A-to-I Human chr7 + 7594362 7594362 7594362 GGAGTCTCATTCTGTCACCCAGACTACAGTGCAACGGCACAATCTCAGCTCACTGCAACTTCCGC GGAGTCTCATTCTGTCACCCAGACTACAGTGCGACGGCACAATCTCAGCTCACTGCAACTTCCGC A G MIOS Ensembl:ENSG00000164654 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs905962799 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_760,RMVar_hsa_circ_359194,RMVar_hsa_circ_243742,RMVar_hsa_circ_266575,RMVar_hsa_circ_285661,RMVar_hsa_circ_72839,RMVar_hsa_circ_95013,RMVar_hsa_circ_243744,RMVar_hsa_circ_243745 48075 RMVar_ID_48075 Human_SNP_ID_309128997 A-to-I Human chr7 + 7594706 7594706 7594706 TCACTGTTTACAACATTCAACCACGAAGTTCTATTTTCTTAAACTTAACTAAAAGGTAGAGAATT TCACTGTTTACAACATTCAACCACGAAGTTCTGTTTTCTTAAACTTAACTAAAAGGTAGAGAATT A G MIOS Ensembl:ENSG00000164654 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6958110 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5804,GWAS_ID_5805,GWAS_ID_5806,GWAS_ID_5807,GWAS_ID_5808,GWAS_ID_5809,GWAS_ID_5810,GWAS_ID_5811 RMVar_hsa_circ_760,RMVar_hsa_circ_359194,RMVar_hsa_circ_243742,RMVar_hsa_circ_266575,RMVar_hsa_circ_285661,RMVar_hsa_circ_72839,RMVar_hsa_circ_95013,RMVar_hsa_circ_243744,RMVar_hsa_circ_243745 48076 RMVar_ID_48076 Human_SNP_ID_309164053 A-to-I Human chr7 + 7717254 7717254 7717254 AATTTTCGTATTTTTGGTAGAGACTGGGTTTCACCACGTTGGCCTGGCTGGTCTCGAACTCCTGA AATTTTCGTATTTTTGGTAGAGACTGGGTTTCCCCACGTTGGCCTGGCTGGTCTCGAACTCCTGA A C AC007161.3,UMAD1 Ensembl:ENSG00000283549,Ensembl:ENSG00000219545 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs905794601 Functional Loss SNV dbSNP153 33..33 33 - - - 48077 RMVar_ID_48077 Human_SNP_ID_309250676 A-to-I Human chr7 + 8041792 8041792 8041792 GTTTTTTATTTTTGTAGAGACAAGGTCTCATTATGTTGCCCAGACTGGTCTCGAACTCCTGGGCT GTTTTTTATTTTTGTAGAGACAAGGTCTCATTGTGTTGCCCAGACTGGTCTCGAACTCCTGGGCT A G GLCCI1 Ensembl:ENSG00000106415 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982939716 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57714,RMVar_hsa_circ_243753,RMVar_hsa_circ_316816,RMVar_hsa_circ_340186,RMVar_hsa_circ_291063,RMVar_hsa_circ_273346,RMVar_hsa_circ_243755,RMVar_hsa_circ_243754,RMVar_hsa_circ_243760,RMVar_hsa_circ_275864,RMVar_hsa_circ_345250,RMVar_hsa_circ_243752,RMVar_hsa_circ_308424,RMVar_hsa_circ_243761,RMVar_hsa_circ_243759 48078 RMVar_ID_48078 Human_SNP_ID_309263623 A-to-I Human chr7 - 8087359 8087359 8087359 GTCCTTTACTGAGCAACACCTGAACTTTTAAAAAAGCCACATGTACACATGTTGAAACAGTGAAT GTCCTTTACTGAGCAACACCTGAACTTTTAAAGAAGCCACATGTACACATGTTGAAACAGTGAAT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1056782360 Functional Loss SNV dbSNP153 33..33 33 - - - 48079 RMVar_ID_48079 Human_SNP_ID_310122352 A-to-I Human chr7 + 11059566 11059566 11059566 GGGAGGCCAAGGCAGGTGGATCGCTTTAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGCAA GGGAGGCCAAGGCAGGTGGATCGCTTTAGGTCGGGAGTTCGAGACCAGCCTGGCCAACATGGCAA A G PHF14 Ensembl:ENSG00000106443 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1298238647 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_374190,RMVar_hsa_circ_309984,RMVar_hsa_circ_320849,RMVar_hsa_circ_243780,RMVar_hsa_circ_302912,RMVar_hsa_circ_316432,RMVar_hsa_circ_243783,RMVar_hsa_circ_319374,RMVar_hsa_circ_366644,RMVar_hsa_circ_243784,RMVar_hsa_circ_243790,RMVar_hsa_circ_300744,RMVar_hsa_circ_295339,RMVar_hsa_circ_295268,RMVar_hsa_circ_243793,RMVar_hsa_circ_243794,RMVar_hsa_circ_326415,RMVar_hsa_circ_90097,RMVar_hsa_circ_243796,RMVar_hsa_circ_243795,RMVar_hsa_circ_75174,RMVar_hsa_circ_243802,RMVar_hsa_circ_111971,RMVar_hsa_circ_56401,RMVar_hsa_circ_243808,RMVar_hsa_circ_243806,RMVar_hsa_circ_300606,RMVar_hsa_circ_243804,RMVar_hsa_circ_338361,RMVar_hsa_circ_272063,RMVar_hsa_circ_243807,RMVar_hsa_circ_290469,RMVar_hsa_circ_327729,RMVar_hsa_circ_243805,RMVar_hsa_circ_327221,RMVar_hsa_circ_283012,RMVar_hsa_circ_243809 48080 RMVar_ID_48080 Human_SNP_ID_310122369 A-to-I Human chr7 + 11059613 11059613 11059613 GCCTGGCCAACATGGCAACCCGTTCTCTAGTAAAAATGAAAAGATTAGCCAGGTGTGGTGGTGCA GCCTGGCCAACATGGCAACCCGTTCTCTAGTAGAAATGAAAAGATTAGCCAGGTGTGGTGGTGCA A G PHF14 Ensembl:ENSG00000106443 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1216453629 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_374190,RMVar_hsa_circ_309984,RMVar_hsa_circ_320849,RMVar_hsa_circ_243780,RMVar_hsa_circ_302912,RMVar_hsa_circ_316432,RMVar_hsa_circ_243783,RMVar_hsa_circ_319374,RMVar_hsa_circ_366644,RMVar_hsa_circ_243784,RMVar_hsa_circ_243790,RMVar_hsa_circ_300744,RMVar_hsa_circ_295339,RMVar_hsa_circ_295268,RMVar_hsa_circ_243793,RMVar_hsa_circ_243794,RMVar_hsa_circ_326415,RMVar_hsa_circ_90097,RMVar_hsa_circ_243796,RMVar_hsa_circ_243795,RMVar_hsa_circ_75174,RMVar_hsa_circ_243802,RMVar_hsa_circ_111971,RMVar_hsa_circ_56401,RMVar_hsa_circ_243808,RMVar_hsa_circ_243806,RMVar_hsa_circ_300606,RMVar_hsa_circ_243804,RMVar_hsa_circ_338361,RMVar_hsa_circ_272063,RMVar_hsa_circ_243807,RMVar_hsa_circ_290469,RMVar_hsa_circ_327729,RMVar_hsa_circ_243805,RMVar_hsa_circ_327221,RMVar_hsa_circ_283012,RMVar_hsa_circ_243809 48081 RMVar_ID_48081 Human_SNP_ID_310124168 A-to-I Human chr7 + 11066308 11066308 11066308 TTTTGTTGTTTGTTTTCGTTGTCACTCAGGCTAGAGTGCAGTGGCACTTTCTTGACGCAGTACAG TTTTGTTGTTTGTTTTCGTTGTCACTCAGGCTGGAGTGCAGTGGCACTTTCTTGACGCAGTACAG A G PHF14 Ensembl:ENSG00000106443 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs564650664 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_374190,RMVar_hsa_circ_309984,RMVar_hsa_circ_243780,RMVar_hsa_circ_366644,RMVar_hsa_circ_300744,RMVar_hsa_circ_295268,RMVar_hsa_circ_243794,RMVar_hsa_circ_243795,RMVar_hsa_circ_75174,RMVar_hsa_circ_243806,RMVar_hsa_circ_272063,RMVar_hsa_circ_243807,RMVar_hsa_circ_327729,RMVar_hsa_circ_283012,RMVar_hsa_circ_243809,RMVar_hsa_circ_275411,RMVar_hsa_circ_243811 48082 RMVar_ID_48082 Human_SNP_ID_310125290 A-to-I Human chr7 + 11070217 11070217 11070217 TTCCCACCTCAGCCTCCTTAGTAGCTGTGACTACAAGTGCGCGCCACCATGCCCAGCTGATTTTT TTCCCACCTCAGCCTCCTTAGTAGCTGTGACTGCAAGTGCGCGCCACCATGCCCAGCTGATTTTT A G PHF14 Ensembl:ENSG00000106443 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs558539521 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26061282 RMVar_hsa_circ_374190,RMVar_hsa_circ_309984,RMVar_hsa_circ_243780,RMVar_hsa_circ_366644,RMVar_hsa_circ_300744,RMVar_hsa_circ_295268,RMVar_hsa_circ_243794,RMVar_hsa_circ_243795,RMVar_hsa_circ_75174,RMVar_hsa_circ_243806,RMVar_hsa_circ_272063,RMVar_hsa_circ_243807,RMVar_hsa_circ_327729,RMVar_hsa_circ_283012,RMVar_hsa_circ_243809,RMVar_hsa_circ_275411,RMVar_hsa_circ_243811 48083 RMVar_ID_48083 Human_SNP_ID_310125308 A-to-I Human chr7 + 11070263 11070263 11070263 CCATGCCCAGCTGATTTTTTAATCGTTTGTAGAAATGGGGTCTGACTGTTTTGCCCAGGCTGGTG CCATGCCCAGCTGATTTTTTAATCGTTTGTAGGAATGGGGTCTGACTGTTTTGCCCAGGCTGGTG A G PHF14 Ensembl:ENSG00000106443 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1413730013 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15977330 RMVar_hsa_circ_374190,RMVar_hsa_circ_309984,RMVar_hsa_circ_243780,RMVar_hsa_circ_366644,RMVar_hsa_circ_300744,RMVar_hsa_circ_295268,RMVar_hsa_circ_243794,RMVar_hsa_circ_243795,RMVar_hsa_circ_75174,RMVar_hsa_circ_243806,RMVar_hsa_circ_272063,RMVar_hsa_circ_243807,RMVar_hsa_circ_327729,RMVar_hsa_circ_283012,RMVar_hsa_circ_243809,RMVar_hsa_circ_275411,RMVar_hsa_circ_243811 48084 RMVar_ID_48084 Human_SNP_ID_310129217 A-to-I Human chr7 + 11083554 11083554 11083554 GCAGTCTCGGCTCACTGGAAACTCCGCCTCCCAGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCCG GCAGTCTCGGCTCACTGGAAACTCCGCCTCCCGGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCCG A G PHF14 Ensembl:ENSG00000106443 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1173883735 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_374190,RMVar_hsa_circ_309984,RMVar_hsa_circ_243780,RMVar_hsa_circ_366644,RMVar_hsa_circ_300744,RMVar_hsa_circ_295268,RMVar_hsa_circ_243794,RMVar_hsa_circ_243795,RMVar_hsa_circ_75174,RMVar_hsa_circ_243806,RMVar_hsa_circ_272063,RMVar_hsa_circ_243807,RMVar_hsa_circ_327729,RMVar_hsa_circ_283012,RMVar_hsa_circ_243809,RMVar_hsa_circ_275411,RMVar_hsa_circ_243811 48085 RMVar_ID_48085 Human_SNP_ID_310331914 A-to-I Human chr7 - 11797495 11797495 11797495 GGAGGATTACTTAAACCTAGGAGGTCAAGGCTACAGTGAGCCAAGATTGTGCCACTGCACTCCAG GGAGGATTACTTAAACCTAGGAGGTCAAGGCTGCAGTGAGCCAAGATTGTGCCACTGCACTCCAG T C THSD7A Ensembl:ENSG00000005108 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1372673857 Functional Loss SNV dbSNP153 33..33 33 - - - 48086 RMVar_ID_48086 Human_SNP_ID_310481814 A-to-I Human chr7 - 12323694 12323681 12323695 GTAATCCCCACTTGTCGAGGGAGGGACTTGGTAGAAGGTGGTTGGATCATGAAGGTGGTTTCCCC GTAATCCCCACTTGTCGAGGGAGGGACTTGG______________ATCATGAAGGTGGTTTCCCC TCCAACCACCTTCTA T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1228505600 Functional Loss DEL dbSNP153 32..45 33 - - - 48087 RMVar_ID_48087 Human_SNP_ID_310490065 A-to-I Human chr7 - 12351893 12351893 12351893 ATGTAGGAGTAGGGATTTAACATATGAATTTTAGGGGAACACAATTCAGTCCATACCAGAAAAGT ATGTAGGAGTAGGGATTTAACATATGAATTTTTGGGGAACACAATTCAGTCCATACCAGAAAAGT T A VWDE Ensembl:ENSG00000146530 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1257858517 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91837,RMVar_hsa_circ_97272,RMVar_hsa_circ_243828,RMVar_hsa_circ_78394,RMVar_hsa_circ_243830,RMVar_hsa_circ_312781,RMVar_hsa_circ_243832,RMVar_hsa_circ_88111,RMVar_hsa_circ_243833,RMVar_hsa_circ_243834,RMVar_hsa_circ_105755,RMVar_hsa_circ_13498,RMVar_hsa_circ_243835,RMVar_hsa_circ_47616,RMVar_hsa_circ_310978,RMVar_hsa_circ_370241,RMVar_hsa_circ_375889,RMVar_hsa_circ_330932,RMVar_hsa_circ_86599,RMVar_hsa_circ_243836,RMVar_hsa_circ_243838,RMVar_hsa_circ_29689,RMVar_hsa_circ_243837 48088 RMVar_ID_48088 Human_SNP_ID_310490072 A-to-I Human chr7 - 12351915 12351915 12351915 CCCTGTCTCCAAACATGTTCACATGTAGGAGTAGGGATTTAACATATGAATTTTAGGGGAACACA CCCTGTCTCCAAACATGTTCACATGTAGGAGTGGGGATTTAACATATGAATTTTAGGGGAACACA T C VWDE Ensembl:ENSG00000146530 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1220019261 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7688394 RMVar_hsa_circ_91837,RMVar_hsa_circ_97272,RMVar_hsa_circ_243828,RMVar_hsa_circ_78394,RMVar_hsa_circ_243830,RMVar_hsa_circ_312781,RMVar_hsa_circ_243832,RMVar_hsa_circ_88111,RMVar_hsa_circ_243833,RMVar_hsa_circ_243834,RMVar_hsa_circ_105755,RMVar_hsa_circ_13498,RMVar_hsa_circ_243835,RMVar_hsa_circ_47616,RMVar_hsa_circ_310978,RMVar_hsa_circ_370241,RMVar_hsa_circ_375889,RMVar_hsa_circ_330932,RMVar_hsa_circ_86599,RMVar_hsa_circ_243836,RMVar_hsa_circ_243838,RMVar_hsa_circ_29689,RMVar_hsa_circ_243837 48089 RMVar_ID_48089 Human_SNP_ID_310577778 A-to-I Human chr7 + 12657358 12657334 12657359 CCCACCTCAGTCTCCCCAGGAGCTGGGACTCTAGGTGCGTGCCACCACGCCCAGCTAATTCTTTG CCCACCTCA_________________________GTGCGTGCCACCACGCCCAGCTAATTCTTTG AGTCTCCCCAGGAGCTGGGACTCTAG A SCIN Ensembl:ENSG00000006747 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1260240134 Functional Loss DEL dbSNP153 10..34 33 - - - 48090 RMVar_ID_48090 Human_SNP_ID_310967367 A-to-I Human chr7 - 13972865 13972865 13972865 GTGGCTCATGCCTATAATCCTGGCACTTTGGAAGGCTGAAGTGGAGAATTGCTTGAGCTCGGGAG GTGGCTCATGCCTATAATCCTGGCACTTTGGAGGGCTGAAGTGGAGAATTGCTTGAGCTCGGGAG T C ETV1 Ensembl:ENSG00000006468 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1357182807 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1631,RMVar_hsa_circ_35570 48091 RMVar_ID_48091 Human_SNP_ID_311144418 A-to-I Human chr7 - 14600189 14600189 14600189 TCAAGGGAACTAGCTCTCGCCTTTCCCCTTCTACTGCCATGTGAAGATACAGCATTCATCCCTCT TCAAGGGAACTAGCTCTCGCCTTTCCCCTTCTGCTGCCATGTGAAGATACAGCATTCATCCCTCT T C DGKB Ensembl:ENSG00000136267 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs978166097 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5693,RMVar_hsa_circ_296641,RMVar_hsa_circ_18701,RMVar_hsa_circ_277867,RMVar_hsa_circ_316511,RMVar_hsa_circ_378294,RMVar_hsa_circ_307500,RMVar_hsa_circ_35853,RMVar_hsa_circ_268489,RMVar_hsa_circ_13086,RMVar_hsa_circ_243858,RMVar_hsa_circ_243854,RMVar_hsa_circ_243856,RMVar_hsa_circ_243855,RMVar_hsa_circ_40817 48092 RMVar_ID_48092 Human_SNP_ID_426886317 A-to-I Human chr10 - 30308715 30308715 30308715 TTTTGTTGTAGAGACAGGGACAGGGTTTCACCATGTTGCTCAGGCTGGTCTTGAACTCCTGGACT TTTTGTTGTAGAGACAGGGACAGGGTTTCACCGTGTTGCTCAGGCTGGTCTTGAACTCCTGGACT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs994669434 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2213567 48093 RMVar_ID_48093 Human_SNP_ID_426886426 A-to-I Human chr10 - 30309176 30309176 30309176 CAGGCCTCAGCCTCCTGAATAGCTGGGATTACAGGCACACACCACCTCACCCAGCTAATTTTTGT CAGGCCTCAGCCTCCTGAATAGCTGGGATTACGGGCACACACCACCTCACCCAGCTAATTTTTGT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935104406 Functional Loss SNV dbSNP153 33..33 33 - - - 48094 RMVar_ID_48094 Human_SNP_ID_426887060 A-to-I Human chr10 - 30311803 30311803 30311803 AGTAAGGCCTGGGCATAGCGGCACATGCCTGTAGTCCCAGGTACTTGGGAGGCCGAGGCACAAGG AGTAAGGCCTGGGCATAGCGGCACATGCCTGTGGTCCCAGGTACTTGGGAGGCCGAGGCACAAGG T C MTPAP Ensembl:ENSG00000107951 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1460971601 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26398882 48095 RMVar_ID_48095 Human_SNP_ID_426887067 A-to-I Human chr10 - 30311819 30311819 30311819 TTCTATTTAAGAAGCAAGTAAGGCCTGGGCATAGCGGCACATGCCTGTAGTCCCAGGTACTTGGG TTCTATTTAAGAAGCAAGTAAGGCCTGGGCATCGCGGCACATGCCTGTAGTCCCAGGTACTTGGG T G MTPAP Ensembl:ENSG00000107951 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs763102450 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26398882 48096 RMVar_ID_48096 Human_SNP_ID_426887152 A-to-I Human chr10 - 30312096 30312096 30312096 AGTTTTGCTCTTGTTGCCCAGGCTGGGGTGCAATGGCACAATCTCAGCTCACTGCAACCTCCGCC AGTTTTGCTCTTGTTGCCCAGGCTGGGGTGCAGTGGCACAATCTCAGCTCACTGCAACCTCCGCC T C MTPAP Ensembl:ENSG00000107951 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11007976 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27405485 48097 RMVar_ID_48097 Human_SNP_ID_426887243 A-to-I Human chr10 - 30312410 30312410 30312410 TGCCCGCCACCACGCCCGGACAATTTTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGGTCT TGCCCGCCACCACGCCCGGACAATTTTTTTGTCTTTTTAGTAGAGACAGGGTTTCACCATGGTCT T G MTPAP Ensembl:ENSG00000107951 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs936955903 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11346911 48098 RMVar_ID_48098 Human_SNP_ID_426887628 A-to-I Human chr10 - 30313693 30313693 30313693 AAAAGCAATAAGTTTGCAATTGAAACAGTCAAAAACTTGCTAGAATCTTTAAAAGGTAACAGAAC AAAAGCAATAAGTTTGCAATTGAAACAGTCAAGAACTTGCTAGAATCTTTAAAAGGTAACAGAAC T C MTPAP Ensembl:ENSG00000107951 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs17855117 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_142895 48099 RMVar_ID_48099 Human_SNP_ID_426890777 A-to-I Human chr10 - 30325637 30325637 30325637 GGTTCAAGCGATTCTTGTGCCTCAGCCTCCCAAGTAGCTGGGATTGTAGATGCATGCCATCACGC GGTTCAAGCGATTCTTGTGCCTCAGCCTCCCAGGTAGCTGGGATTGTAGATGCATGCCATCACGC T C MTPAP Ensembl:ENSG00000107951 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1260767283 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_142897,RMVar_hsa_circ_142895,RMVar_hsa_circ_142898,RMVar_hsa_circ_46623,RMVar_hsa_circ_142896,RMVar_hsa_circ_100201,RMVar_hsa_circ_64876,RMVar_hsa_circ_142904,RMVar_hsa_circ_302109,RMVar_hsa_circ_340992,RMVar_hsa_circ_142902,RMVar_hsa_circ_319501,RMVar_hsa_circ_142905 48100 RMVar_ID_48100 Human_SNP_ID_426891668 A-to-I Human chr10 - 30329165 30329165 30329165 CGGCTCACTGCAACCTTGGCCTCCTGGGTTCAAGCTATTCTCCTGCTTCAGCCTCCTGAGTAGCT CGGCTCACTGCAACCTTGGCCTCCTGGGTTCAGGCTATTCTCCTGCTTCAGCCTCCTGAGTAGCT T C MTPAP Ensembl:ENSG00000107951 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1402812071 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_142897,RMVar_hsa_circ_142895,RMVar_hsa_circ_142898,RMVar_hsa_circ_46623,RMVar_hsa_circ_142896,RMVar_hsa_circ_100201,RMVar_hsa_circ_64876,RMVar_hsa_circ_302109,RMVar_hsa_circ_142902,RMVar_hsa_circ_319501,RMVar_hsa_circ_142905,RMVar_hsa_circ_142907,RMVar_hsa_circ_372075,RMVar_hsa_circ_347665,RMVar_hsa_circ_142906 48101 RMVar_ID_48101 Human_SNP_ID_427031112 A-to-I Human chr10 - 30851942 30851942 30851942 CGTGGCCAGGTTGGTTTCAAGCTCCTGACCTCAAGTGATCCGCCCATCTCAGCCTCCCAAAGTGC CGTGGCCAGGTTGGTTTCAAGCTCCTGACCTCGAGTGATCCGCCCATCTCAGCCTCCCAAAGTGC T C ZNF438 Ensembl:ENSG00000183621 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1370089553 Functional Loss SNV dbSNP153 33..33 33 - - - 48102 RMVar_ID_48102 Human_SNP_ID_427059532 A-to-I Human chr10 - 30968504 30968504 30968504 GGGAGGTGGAGGTTGTGGTGAGCCGAGATCACACCATTGCACTCCAGCCTGGGCAACAAGAGCGA GGGAGGTGGAGGTTGTGGTGAGCCGAGATCACGCCATTGCACTCCAGCCTGGGCAACAAGAGCGA T C ZNF438 Ensembl:ENSG00000183621 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1012821946 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14364,RMVar_hsa_circ_291494,RMVar_hsa_circ_142920,RMVar_hsa_circ_142921,RMVar_hsa_circ_303549,RMVar_hsa_circ_142923,RMVar_hsa_circ_305206 48103 RMVar_ID_48103 Human_SNP_ID_427059559 A-to-I Human chr10 - 30968622 30968622 30968622 CCAGACCAACATGGAGAAACCCCATCTCTACTAAAAATACAAAATTAGCCAGGTGTGGTGGTGCA CCAGACCAACATGGAGAAACCCCATCTCTACTGAAAATACAAAATTAGCCAGGTGTGGTGGTGCA T C ZNF438 Ensembl:ENSG00000183621 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1236801201 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14364,RMVar_hsa_circ_291494,RMVar_hsa_circ_142920,RMVar_hsa_circ_142921,RMVar_hsa_circ_303549,RMVar_hsa_circ_142923,RMVar_hsa_circ_305206 48104 RMVar_ID_48104 Human_SNP_ID_427158054 A-to-I Human chr10 + 31381832 31381832 31381832 CAGGAGTTCAAGACCAGCCTGGCCAACATGGTAAAACCCCATCTCTACTAAAAATAGAGAAATTA CAGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATAGAGAAATTA A G ZEB1 Ensembl:ENSG00000148516 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs946798261 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_70972,RMVar_hsa_circ_272871,RMVar_hsa_circ_303023,RMVar_hsa_circ_142935,RMVar_hsa_circ_142936,RMVar_hsa_circ_356957,RMVar_hsa_circ_279281,RMVar_hsa_circ_298831,RMVar_hsa_circ_273635,RMVar_hsa_circ_111556,RMVar_hsa_circ_126352,RMVar_hsa_circ_26726,RMVar_hsa_circ_142939,RMVar_hsa_circ_142941,RMVar_hsa_circ_142942,RMVar_hsa_circ_142940,RMVar_hsa_circ_142938,RMVar_hsa_circ_281504,RMVar_hsa_circ_298968,RMVar_hsa_circ_115640,RMVar_hsa_circ_142943,RMVar_hsa_circ_142944 48105 RMVar_ID_48105 Human_SNP_ID_427158707 A-to-I Human chr10 + 31384185 31384185 31384185 TTTAGTAGAGACGGGGTTTCTCCATGTTTCCCAGGCTGGTCTGGAGTTCCTGAGCTCAAATAATT TTTAGTAGAGACGGGGTTTCTCCATGTTTCCCGGGCTGGTCTGGAGTTCCTGAGCTCAAATAATT A G ZEB1 Ensembl:ENSG00000148516 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1483094773 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_70972,RMVar_hsa_circ_272871,RMVar_hsa_circ_303023,RMVar_hsa_circ_142935,RMVar_hsa_circ_142936,RMVar_hsa_circ_356957,RMVar_hsa_circ_279281,RMVar_hsa_circ_298831,RMVar_hsa_circ_273635,RMVar_hsa_circ_111556,RMVar_hsa_circ_126352,RMVar_hsa_circ_26726,RMVar_hsa_circ_142939,RMVar_hsa_circ_142941,RMVar_hsa_circ_142942,RMVar_hsa_circ_142940,RMVar_hsa_circ_142938,RMVar_hsa_circ_281504,RMVar_hsa_circ_298968,RMVar_hsa_circ_115640,RMVar_hsa_circ_142943,RMVar_hsa_circ_142944 48106 RMVar_ID_48106 Human_SNP_ID_427317210 A-to-I Human chr10 - 32016004 32016004 32016004 AAGTAGCTGGGACTACAGGTGCACGCCACCACACCTAGCTAATTTTTTTATATTCTGTAGAGACA AAGTAGCTGGGACTACAGGTGCACGCCACCACCCCTAGCTAATTTTTTTATATTCTGTAGAGACA T G KIF5B Ensembl:ENSG00000170759 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1168339232 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40472,RMVar_hsa_circ_142975,RMVar_hsa_circ_76283,RMVar_hsa_circ_125216,RMVar_hsa_circ_107016,RMVar_hsa_circ_110863,RMVar_hsa_circ_106204,RMVar_hsa_circ_142977,RMVar_hsa_circ_142978,RMVar_hsa_circ_142979,RMVar_hsa_circ_142976,RMVar_hsa_circ_91128,RMVar_hsa_circ_308890,RMVar_hsa_circ_361440,RMVar_hsa_circ_374773,RMVar_hsa_circ_342000,RMVar_hsa_circ_358426,RMVar_hsa_circ_332969,RMVar_hsa_circ_124160,RMVar_hsa_circ_286590,RMVar_hsa_circ_122734,RMVar_hsa_circ_88440,RMVar_hsa_circ_89032,RMVar_hsa_circ_64869,RMVar_hsa_circ_142984,RMVar_hsa_circ_142986,RMVar_hsa_circ_142988,RMVar_hsa_circ_142990,RMVar_hsa_circ_142991,RMVar_hsa_circ_142989,RMVar_hsa_circ_142987,RMVar_hsa_circ_142985,RMVar_hsa_circ_142982,RMVar_hsa_circ_142983,RMVar_hsa_circ_142981 48107 RMVar_ID_48107 Human_SNP_ID_427317432 A-to-I Human chr10 - 32016705 32016705 32016705 TGAAACCCTGTCTCTACTAAATAAAAAAAATTAGCCAGGCATGGTGGTGAACGCCTGTAACCCAG TGAAACCCTGTCTCTACTAAATAAAAAAAATTGGCCAGGCATGGTGGTGAACGCCTGTAACCCAG T C KIF5B Ensembl:ENSG00000170759 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1170271551 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_11349967 RMVar_hsa_circ_40472,RMVar_hsa_circ_142975,RMVar_hsa_circ_76283,RMVar_hsa_circ_125216,RMVar_hsa_circ_107016,RMVar_hsa_circ_110863,RMVar_hsa_circ_106204,RMVar_hsa_circ_142977,RMVar_hsa_circ_142978,RMVar_hsa_circ_142979,RMVar_hsa_circ_142976,RMVar_hsa_circ_91128,RMVar_hsa_circ_308890,RMVar_hsa_circ_361440,RMVar_hsa_circ_374773,RMVar_hsa_circ_342000,RMVar_hsa_circ_358426,RMVar_hsa_circ_332969,RMVar_hsa_circ_124160,RMVar_hsa_circ_286590,RMVar_hsa_circ_122734,RMVar_hsa_circ_88440,RMVar_hsa_circ_89032,RMVar_hsa_circ_64869,RMVar_hsa_circ_142984,RMVar_hsa_circ_142986,RMVar_hsa_circ_142988,RMVar_hsa_circ_142990,RMVar_hsa_circ_142991,RMVar_hsa_circ_142989,RMVar_hsa_circ_142987,RMVar_hsa_circ_142985,RMVar_hsa_circ_142982,RMVar_hsa_circ_142983,RMVar_hsa_circ_142981 48108 RMVar_ID_48108 Human_SNP_ID_427319671 A-to-I Human chr10 - 32024678 32024678 32024678 TCACTGCAAGCTCCTCTTCCTGGGTTCAAGCAATTCTTCTGCCTCAGCCTCCCGAGTAGCTGGGA TCACTGCAAGCTCCTCTTCCTGGGTTCAAGCATTTCTTCTGCCTCAGCCTCCCGAGTAGCTGGGA T A KIF5B Ensembl:ENSG00000170759 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1405445624 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_143000,RMVar_hsa_circ_92664,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_20932 48109 RMVar_ID_48109 Human_SNP_ID_427319672 A-to-I Human chr10 - 32024682 32024682 32024682 CGGCTCACTGCAAGCTCCTCTTCCTGGGTTCAAGCAATTCTTCTGCCTCAGCCTCCCGAGTAGCT CGGCTCACTGCAAGCTCCTCTTCCTGGGTTCAGGCAATTCTTCTGCCTCAGCCTCCCGAGTAGCT T C KIF5B Ensembl:ENSG00000170759 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs981619353 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_143000,RMVar_hsa_circ_92664,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_20932 48110 RMVar_ID_48110 Human_SNP_ID_427383994 A-to-I Human chr10 - 32271173 32271173 32271173 CAGCCGATCCAACATGGTGAAAGGCCACCTCTACTAAAAATACAAAATCACCCGGGCATGGTGGC CAGCCGATCCAACATGGTGAAAGGCCACCTCTGCTAAAAATACAAAATCACCCGGGCATGGTGGC T C EPC1 Ensembl:ENSG00000120616 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs890216094 Functional Loss SNV dbSNP153 33..33 33 - - - 48111 RMVar_ID_48111 Human_SNP_ID_427386316 A-to-I Human chr10 - 32280262 32280262 32280262 TTAGTAGAGACGGGGTTTCACCATGTTGGCCAAGCTGGTCTTGAACTCCTGACCTCAAGTGATCC TTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGACCTCAAGTGATCC T C EPC1 Ensembl:ENSG00000120616 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1273354106 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45956,RMVar_hsa_circ_85336,RMVar_hsa_circ_344818,RMVar_hsa_circ_143021,RMVar_hsa_circ_143020,RMVar_hsa_circ_143024,RMVar_hsa_circ_80823,RMVar_hsa_circ_143023 48112 RMVar_ID_48112 Human_SNP_ID_427386353 A-to-I Human chr10 - 32280437 32280437 32280437 CGTGCCTGGCCTTTTTTTTGAGATACAGTTTCACTCTGTCTCCCAGGCTGGAGTGCCATGGCGTG CGTGCCTGGCCTTTTTTTTGAGATACAGTTTCGCTCTGTCTCCCAGGCTGGAGTGCCATGGCGTG T C EPC1 Ensembl:ENSG00000120616 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1330769896 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45956,RMVar_hsa_circ_85336,RMVar_hsa_circ_344818,RMVar_hsa_circ_143021,RMVar_hsa_circ_143020,RMVar_hsa_circ_143024,RMVar_hsa_circ_80823,RMVar_hsa_circ_143023 48113 RMVar_ID_48113 Human_SNP_ID_427386835 A-to-I Human chr10 - 32282404 32282404 32282404 GTGATCCCCCAACCTCAGCCTCCTGGGTAGCTAGGACTGCAGGCGTATGCCACCATGACTGGCTA GTGATCCCCCAACCTCAGCCTCCTGGGTAGCTTGGACTGCAGGCGTATGCCACCATGACTGGCTA T A EPC1 Ensembl:ENSG00000120616 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054613200 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_45956,RMVar_hsa_circ_85336,RMVar_hsa_circ_344818,RMVar_hsa_circ_143021,RMVar_hsa_circ_143020,RMVar_hsa_circ_143024,RMVar_hsa_circ_80823,RMVar_hsa_circ_143023 48114 RMVar_ID_48114 Human_SNP_ID_427388375 A-to-I Human chr10 - 32288667 32288667 32288667 ATTATTTGCTTTCCTCTATATGTGCCACTCATACTTGAAAGTTACTTTAGGCCGGGTGCAGCAGC ATTATTTGCTTTCCTCTATATGTGCCACTCATTCTTGAAAGTTACTTTAGGCCGGGTGCAGCAGC T A EPC1 Ensembl:ENSG00000120616 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7910034 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85336,RMVar_hsa_circ_143021,RMVar_hsa_circ_143024,RMVar_hsa_circ_80823,RMVar_hsa_circ_143023,RMVar_hsa_circ_45266,RMVar_hsa_circ_143027,RMVar_hsa_circ_307506,RMVar_hsa_circ_27870 48115 RMVar_ID_48115 Human_SNP_ID_427388376 A-to-I Human chr10 - 32288667 32288667 32288667 ATTATTTGCTTTCCTCTATATGTGCCACTCATACTTGAAAGTTACTTTAGGCCGGGTGCAGCAGC ATTATTTGCTTTCCTCTATATGTGCCACTCATGCTTGAAAGTTACTTTAGGCCGGGTGCAGCAGC T C EPC1 Ensembl:ENSG00000120616 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7910034 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85336,RMVar_hsa_circ_143021,RMVar_hsa_circ_143024,RMVar_hsa_circ_80823,RMVar_hsa_circ_143023,RMVar_hsa_circ_45266,RMVar_hsa_circ_143027,RMVar_hsa_circ_307506,RMVar_hsa_circ_27870 48116 RMVar_ID_48116 Human_SNP_ID_427388422 A-to-I Human chr10 - 32288810 32288810 32288810 GCTGGGATTACAGGCATGAGCCACCCCACCCGACCTCCCACTCTTAACTATTTTAATGTGGTCCC GCTGGGATTACAGGCATGAGCCACCCCACCCGGCCTCCCACTCTTAACTATTTTAATGTGGTCCC T C EPC1 Ensembl:ENSG00000120616 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6481784 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85336,RMVar_hsa_circ_143021,RMVar_hsa_circ_143024,RMVar_hsa_circ_80823,RMVar_hsa_circ_143023,RMVar_hsa_circ_45266,RMVar_hsa_circ_143027,RMVar_hsa_circ_307506,RMVar_hsa_circ_27870 48117 RMVar_ID_48117 Human_SNP_ID_427388858 A-to-I Human chr10 - 32290434 32290434 32290434 TCACCCGGGCTGGAGTGCAGTGGCCGGATCTCAGCACACTGCAACCTCCACCTCCCGAGTTTAAG TCACCCGGGCTGGAGTGCAGTGGCCGGATCTCGGCACACTGCAACCTCCACCTCCCGAGTTTAAG T C EPC1 Ensembl:ENSG00000120616 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs995172338 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85336,RMVar_hsa_circ_143021,RMVar_hsa_circ_143024,RMVar_hsa_circ_80823,RMVar_hsa_circ_143023,RMVar_hsa_circ_45266,RMVar_hsa_circ_143027,RMVar_hsa_circ_307506,RMVar_hsa_circ_27870 48118 RMVar_ID_48118 Human_SNP_ID_427389027 A-to-I Human chr10 - 32290763 32290763 32290763 CTAAAAAAAAAAAGATAAAAAAAGAAAAATACATATATACCCCACCTTAATGTATACTGCAATGA CTAAAAAAAAAAAGATAAAAAAAGAAAAATACTTATATACCCCACCTTAATGTATACTGCAATGA T A EPC1 Ensembl:ENSG00000120616 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs3006623 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85336,RMVar_hsa_circ_143021,RMVar_hsa_circ_143024,RMVar_hsa_circ_80823,RMVar_hsa_circ_143023,RMVar_hsa_circ_45266,RMVar_hsa_circ_143027,RMVar_hsa_circ_307506,RMVar_hsa_circ_27870 48119 RMVar_ID_48119 Human_SNP_ID_427389028 A-to-I Human chr10 - 32290763 32290763 32290763 CTAAAAAAAAAAAGATAAAAAAAGAAAAATACATATATACCCCACCTTAATGTATACTGCAATGA CTAAAAAAAAAAAGATAAAAAAAGAAAAATACGTATATACCCCACCTTAATGTATACTGCAATGA T C EPC1 Ensembl:ENSG00000120616 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs3006623 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85336,RMVar_hsa_circ_143021,RMVar_hsa_circ_143024,RMVar_hsa_circ_80823,RMVar_hsa_circ_143023,RMVar_hsa_circ_45266,RMVar_hsa_circ_143027,RMVar_hsa_circ_307506,RMVar_hsa_circ_27870 48120 RMVar_ID_48120 Human_SNP_ID_427389053 A-to-I Human chr10 - 32290842 32290842 32290842 TGAATCCAGGAGGTGGAGGTTGCAGTGAGCCAAGATCACACCATTGCACTCCAGCCTGGGTGACA TGAATCCAGGAGGTGGAGGTTGCAGTGAGCCAGGATCACACCATTGCACTCCAGCCTGGGTGACA T C EPC1 Ensembl:ENSG00000120616 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1188638406 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85336,RMVar_hsa_circ_143021,RMVar_hsa_circ_143024,RMVar_hsa_circ_80823,RMVar_hsa_circ_143023,RMVar_hsa_circ_45266,RMVar_hsa_circ_143027,RMVar_hsa_circ_307506,RMVar_hsa_circ_27870 48121 RMVar_ID_48121 Human_SNP_ID_427389070 A-to-I Human chr10 - 32290912 32290912 32290912 AAATTAGCCAGGTATGGTGGCATGCGCCTGCAATCCCAGCTACTAGGGAGGCTGAGACAGGAGAA AAATTAGCCAGGTATGGTGGCATGCGCCTGCAGTCCCAGCTACTAGGGAGGCTGAGACAGGAGAA T C EPC1 Ensembl:ENSG00000120616 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs139818586 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85336,RMVar_hsa_circ_143021,RMVar_hsa_circ_143024,RMVar_hsa_circ_80823,RMVar_hsa_circ_143023,RMVar_hsa_circ_45266,RMVar_hsa_circ_143027,RMVar_hsa_circ_307506,RMVar_hsa_circ_27870 48122 RMVar_ID_48122 Human_SNP_ID_427389873 A-to-I Human chr10 - 32294507 32294507 32294507 AATGCTCCGCAGTTCGAAATTTTTGAGCACCAATGTGATTCCACGTGTGGAAAATTATACACCTG AATGCTCCGCAGTTCGAAATTTTTGAGCACCAGTGTGATTCCACGTGTGGAAAATTATACACCTG T C EPC1 Ensembl:ENSG00000120616 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2505379 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5812,GWAS_ID_5813,GWAS_ID_5814,GWAS_ID_5815,GWAS_ID_5816,GWAS_ID_5817,GWAS_ID_5818,GWAS_ID_5819,GWAS_ID_5820,GWAS_ID_5821,GWAS_ID_5822,GWAS_ID_5823,GWAS_ID_5824,GWAS_ID_5825,GWAS_ID_5826,GWAS_ID_5827,GWAS_ID_5828,GWAS_ID_5829,GWAS_ID_5830,GWAS_ID_5831 RMVar_hsa_circ_26651,RMVar_hsa_circ_80823,RMVar_hsa_circ_143023,RMVar_hsa_circ_45266,RMVar_hsa_circ_143030,RMVar_hsa_circ_376443 48123 RMVar_ID_48123 Human_SNP_ID_427406056 A-to-I Human chr10 - 32357966 32357966 32357966 CCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCTCATGAATCCGGGAGGTGGAGGTT CCTGTAATCCCAGCTACTCGGGAGGCTGAGGCGGGAGAATCTCATGAATCCGGGAGGTGGAGGTT T C EPC1 Ensembl:ENSG00000120616 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1416395232 Functional Loss SNV dbSNP153 33..33 33 - - - 48124 RMVar_ID_48124 Human_SNP_ID_427541833 A-to-I Human chr10 - 32895724 32895724 32895724 TCATATATGGGACAGTGGCCATATATTGCCATAAAAGGAATGGAGTTTTGATACAACATGGTGAG TCATATATGGGACAGTGGCCATATATTGCCATTAAAGGAATGGAGTTTTGATACAACATGGTGAG T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459106823 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2214980,Human_RBP_ID_8333512 48125 RMVar_ID_48125 Human_SNP_ID_427541834 A-to-I Human chr10 - 32895724 32895724 32895724 TCATATATGGGACAGTGGCCATATATTGCCATAAAAGGAATGGAGTTTTGATACAACATGGTGAG TCATATATGGGACAGTGGCCATATATTGCCATGAAAGGAATGGAGTTTTGATACAACATGGTGAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459106823 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2214980,Human_RBP_ID_8333512 48126 RMVar_ID_48126 Human_SNP_ID_427541864 A-to-I Human chr10 - 32895848 32895848 32895848 ATTTGAAAGTAGGGACTTAAACAGATATTTACATGCTCATATTAATTGCAGCATTATTCACAGTA ATTTGAAAGTAGGGACTTAAACAGATATTTACGTGCTCATATTAATTGCAGCATTATTCACAGTA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs949086873 Functional Loss SNV dbSNP153 33..33 33 - - - 48127 RMVar_ID_48127 Human_SNP_ID_427541878 A-to-I Human chr10 - 32895921 32895921 32895921 CACCCCCTCAAAGAGCTAAACATAAAATTACCATATGACCCCTCAATTCTACTTTTAGATTTATA CACCCCCTCAAAGAGCTAAACATAAAATTACCGTATGACCCCTCAATTCTACTTTTAGATTTATA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1442108318 Functional Loss SNV dbSNP153 33..33 33 - - - 48128 RMVar_ID_48128 Human_SNP_ID_427542153 A-to-I Human chr10 - 32897275 32897275 32897275 TTATATGCCTAAAAGAAGAATTGCTGGATCATATAGTAATTGTGTTTTGCTCTTTGAGGAACTGC TTATATGCCTAAAAGAAGAATTGCTGGATCATGTAGTAATTGTGTTTTGCTCTTTGAGGAACTGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs537625030 Functional Loss SNV dbSNP153 33..33 33 - - - 48129 RMVar_ID_48129 Human_SNP_ID_427559199 A-to-I Human chr10 + 32964276 32964276 32964276 AAAATTAGTTGGCCGTGGTGACTCGTGCCAGTAGTCCCAGCTACTTAGGAGGGTGAGGCACAAGA AAAATTAGTTGGCCGTGGTGACTCGTGCCAGTGGTCCCAGCTACTTAGGAGGGTGAGGCACAAGA A G ITGB1-DT Ensembl:ENSG00000229656 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978010506 Functional Loss SNV dbSNP153 33..33 33 - - - 48130 RMVar_ID_48130 Human_SNP_ID_427615163 A-to-I Human chr10 - 33187072 33187072 33187072 GGCCAGGAGTTTGAGACTAGCCTGGGCAACATAGCAAGATTCTATCTCTACTTAAAAAAAAAAAT GGCCAGGAGTTTGAGACTAGCCTGGGCAACATGGCAAGATTCTATCTCTACTTAAAAAAAAAAAT T C NRP1 Ensembl:ENSG00000099250 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1180184029 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1233,RMVar_hsa_circ_267759,RMVar_hsa_circ_67188,RMVar_hsa_circ_326739,RMVar_hsa_circ_327205 48131 RMVar_ID_48131 Human_SNP_ID_427915848 A-to-I Human chr10 - 34370479 34370479 34370479 GCCCAGGAGATTAAGACCAGTCTGGGCAACACAGCGAGACCTCATCTCTACCAAAAAGTTAAAAA GCCCAGGAGATTAAGACCAGTCTGGGCAACACGGCGAGACCTCATCTCTACCAAAAAGTTAAAAA T C PARD3 Ensembl:ENSG00000148498 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1282704112 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118270,RMVar_hsa_circ_143103,RMVar_hsa_circ_14051,RMVar_hsa_circ_58624,RMVar_hsa_circ_37203,RMVar_hsa_circ_318543,RMVar_hsa_circ_368810,RMVar_hsa_circ_358526,RMVar_hsa_circ_69491,RMVar_hsa_circ_280660,RMVar_hsa_circ_67463,RMVar_hsa_circ_59130,RMVar_hsa_circ_29420,RMVar_hsa_circ_55561,RMVar_hsa_circ_143105,RMVar_hsa_circ_299249,RMVar_hsa_circ_303183,RMVar_hsa_circ_357519,RMVar_hsa_circ_314510,RMVar_hsa_circ_110293,RMVar_hsa_circ_348577,RMVar_hsa_circ_272217,RMVar_hsa_circ_143116,RMVar_hsa_circ_143117,RMVar_hsa_circ_56482,RMVar_hsa_circ_268786,RMVar_hsa_circ_143124,RMVar_hsa_circ_62009,RMVar_hsa_circ_70336,RMVar_hsa_circ_16749,RMVar_hsa_circ_336140,RMVar_hsa_circ_370578,RMVar_hsa_circ_143120,RMVar_hsa_circ_143121,RMVar_hsa_circ_303903,RMVar_hsa_circ_95928,RMVar_hsa_circ_143122,RMVar_hsa_circ_357215,RMVar_hsa_circ_294888,RMVar_hsa_circ_55956,RMVar_hsa_circ_143125,RMVar_hsa_circ_17025,RMVar_hsa_circ_352674,RMVar_hsa_circ_365566,RMVar_hsa_circ_377274,RMVar_hsa_circ_358304,RMVar_hsa_circ_323533,RMVar_hsa_circ_274034,RMVar_hsa_circ_143127 48132 RMVar_ID_48132 Human_SNP_ID_427981560 A-to-I Human chr10 - 34631754 34631754 34631754 GTTTTTACAGAAAATAAAAAATTTAACCAGATATAGTGGCATGTGCATATAGTCTCAGCTACTCA GTTTTTACAGAAAATAAAAAATTTAACCAGATGTAGTGGCATGTGCATATAGTCTCAGCTACTCA T C PARD3 Ensembl:ENSG00000148498 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1423604523 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69491,RMVar_hsa_circ_29420,RMVar_hsa_circ_55956,RMVar_hsa_circ_18368,RMVar_hsa_circ_365566,RMVar_hsa_circ_40423,RMVar_hsa_circ_143135,RMVar_hsa_circ_126043,RMVar_hsa_circ_315714,RMVar_hsa_circ_317514,RMVar_hsa_circ_277135 48133 RMVar_ID_48133 Human_SNP_ID_427985085 A-to-I Human chr10 - 34645343 34645343 34645343 AAATTAGTTGGGCGTGGTGGTATGCGCCTGTAATTCCAGCTACTGGGGAGGCTGAGGCATGAGAA AAATTAGTTGGGCGTGGTGGTATGCGCCTGTAGTTCCAGCTACTGGGGAGGCTGAGGCATGAGAA T C PARD3 Ensembl:ENSG00000148498 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1218356927 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69491,RMVar_hsa_circ_29420,RMVar_hsa_circ_55956,RMVar_hsa_circ_18368,RMVar_hsa_circ_365566,RMVar_hsa_circ_40423,RMVar_hsa_circ_143135,RMVar_hsa_circ_126043,RMVar_hsa_circ_315714,RMVar_hsa_circ_317514,RMVar_hsa_circ_277135 48134 RMVar_ID_48134 Human_SNP_ID_427994175 A-to-I Human chr10 - 34680444 34680444 34680444 AGTGATCTCCTGCCTCATCCTCCAGAGTAGCTAGGATTACAGGCTCCCACCACCATACCTGGCTA AGTGATCTCCTGCCTCATCCTCCAGAGTAGCTGGGATTACAGGCTCCCACCACCATACCTGGCTA T C PARD3 Ensembl:ENSG00000148498 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1293001661 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69491,RMVar_hsa_circ_29420,RMVar_hsa_circ_55956,RMVar_hsa_circ_18368,RMVar_hsa_circ_365566,RMVar_hsa_circ_40423,RMVar_hsa_circ_143135,RMVar_hsa_circ_126043,RMVar_hsa_circ_315714,RMVar_hsa_circ_317514,RMVar_hsa_circ_277135 48135 RMVar_ID_48135 Human_SNP_ID_428013987 A-to-I Human chr10 - 34755156 34755156 34755156 CTCAAGTGATCTGCCCGCCTCAGCCTCCCAAAATGCTGGGATCACAGGCATGAGCCACCGCGCCC CTCAAGTGATCTGCCCGCCTCAGCCTCCCAAAGTGCTGGGATCACAGGCATGAGCCACCGCGCCC T C PARD3 Ensembl:ENSG00000148498 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs896733374 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_143135,RMVar_hsa_circ_126043 48136 RMVar_ID_48136 Human_SNP_ID_428026539 A-to-I Human chr10 - 34803654 34803654 34803654 GGATTATAGGTTCCAGCCACCACACCTGGCTAAATTTTTGTATTTTTAGTAGAGATGGGGTTTCA GGATTATAGGTTCCAGCCACCACACCTGGCTACATTTTTGTATTTTTAGTAGAGATGGGGTTTCA T G PARD3 Ensembl:ENSG00000148498 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992145646 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_143135,RMVar_hsa_circ_126043 48137 RMVar_ID_48137 Human_SNP_ID_428093490 A-to-I Human chr10 - 35064822 35064822 35064822 ACATGCAGTGGATATATTGAGCGGTGGCTCATACCTGTAATCCTAGCACTTTGGGAGGCCGAGGC ACATGCAGTGGATATATTGAGCGGTGGCTCATGCCTGTAATCCTAGCACTTTGGGAGGCCGAGGC T C CUL2 Ensembl:ENSG00000108094 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs942030477 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_306426,RMVar_hsa_circ_143145,RMVar_hsa_circ_325797,RMVar_hsa_circ_143148,RMVar_hsa_circ_351503,RMVar_hsa_circ_143160,RMVar_hsa_circ_143167,RMVar_hsa_circ_35314,RMVar_hsa_circ_143161,RMVar_hsa_circ_370011,RMVar_hsa_circ_363354,RMVar_hsa_circ_143162,RMVar_hsa_circ_319817,RMVar_hsa_circ_291540,RMVar_hsa_circ_143163,RMVar_hsa_circ_267535,RMVar_hsa_circ_143168,RMVar_hsa_circ_281338,RMVar_hsa_circ_143169,RMVar_hsa_circ_297797,RMVar_hsa_circ_293721,RMVar_hsa_circ_143171 48138 RMVar_ID_48138 Human_SNP_ID_428099286 A-to-I Human chr10 - 35087261 35087261 35087261 ATGGCTCAAAATTTAAGATGTTAGTCTGGGCAACATGGTGAGACCCCATGTCTACAAAAAATAAT ATGGCTCAAAATTTAAGATGTTAGTCTGGGCAGCATGGTGAGACCCCATGTCTACAAAAAATAAT T C CUL2 Ensembl:ENSG00000108094 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1156700086 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267535 48139 RMVar_ID_48139 Human_SNP_ID_428115266 A-to-I Human chr10 + 35150700 35150700 35150700 AAAACTAGGTGGTTATGGTGGCACACGCCTGTAGTCGCAGCTGCTCGGGAGGCTGAGGCACGAGA AAAACTAGGTGGTTATGGTGGCACACGCCTGTCGTCGCAGCTGCTCGGGAGGCTGAGGCACGAGA A C CREM Ensembl:ENSG00000095794 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs916350988 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106095,RMVar_hsa_circ_143175,RMVar_hsa_circ_55519,RMVar_hsa_circ_355362,RMVar_hsa_circ_143174,RMVar_hsa_circ_353032,RMVar_hsa_circ_76865,RMVar_hsa_circ_50647,RMVar_hsa_circ_111402,RMVar_hsa_circ_319833,RMVar_hsa_circ_350976,RMVar_hsa_circ_293398,RMVar_hsa_circ_143176 48140 RMVar_ID_48140 Human_SNP_ID_428129002 A-to-I Human chr10 + 35203530 35203530 35203530 CCTGGCCAGAATGGTGAAATCTCATCTCTACTAAACATACAAAAATTAGCTGGGAGCGGTGGTGG CCTGGCCAGAATGGTGAAATCTCATCTCTACTGAACATACAAAAATTAGCTGGGAGCGGTGGTGG A G CREM Ensembl:ENSG00000095794 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1216769937 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_53470,RMVar_hsa_circ_353032,RMVar_hsa_circ_319833,RMVar_hsa_circ_274517,RMVar_hsa_circ_367443,RMVar_hsa_circ_143177,RMVar_hsa_circ_276041,RMVar_hsa_circ_143179,RMVar_hsa_circ_143178,RMVar_hsa_circ_143180,RMVar_hsa_circ_320834 48141 RMVar_ID_48141 Human_SNP_ID_428156837 A-to-I Human chr10 - 35318045 35318045 35318045 TTTGAAATTTTTTGTAGAAATGAGGTCTCCCTATGTTGCCCAGGCTGGTCTTGAACTCCTGGCCT TTTGAAATTTTTTGTAGAAATGAGGTCTCCCTCTGTTGCCCAGGCTGGTCTTGAACTCCTGGCCT T G AL117336.2 Ensembl:ENSG00000271335 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941427741 Functional Loss SNV dbSNP153 33..33 33 - - - 48142 RMVar_ID_48142 Human_SNP_ID_428156851 A-to-I Human chr10 - 35318133 35318133 35318133 GCCTAGAACTCCTGGGCTCAAGTGATGTTCCCACCTTAGCCTCCTGAGTAGCTGGGACTATAGAC GCCTAGAACTCCTGGGCTCAAGTGATGTTCCCGCCTTAGCCTCCTGAGTAGCTGGGACTATAGAC T C AL117336.2 Ensembl:ENSG00000271335 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1312357976 Functional Loss SNV dbSNP153 33..33 33 - - - 48143 RMVar_ID_48143 Human_SNP_ID_428157026 A-to-I Human chr10 - 35319005 35319005 35319005 TGAGCCGTGATCCCGCCACTGCACTCCGGCCCAGGTGACACTATGAGACTCTGTCTCAAAAAAAT TGAGCCGTGATCCCGCCACTGCACTCCGGCCCGGGTGACACTATGAGACTCTGTCTCAAAAAAAT T C AL117336.2 Ensembl:ENSG00000271335 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs764734578 Functional Loss SNV dbSNP153 33..33 33 - - - 48144 RMVar_ID_48144 Human_SNP_ID_428157098 A-to-I Human chr10 - 35319336 35319336 35319336 ATTCTGTCACCCAGACCAGGCTGGAATACAGTAGCGATCATAACTCACTCAGCCCCAAACTCCTG ATTCTGTCACCCAGACCAGGCTGGAATACAGTGGCGATCATAACTCACTCAGCCCCAAACTCCTG T C AL117336.2 Ensembl:ENSG00000271335 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1476686456 Functional Loss SNV dbSNP153 33..33 33 - - - 48145 RMVar_ID_48145 Human_SNP_ID_428157449 A-to-I Human chr10 - 35321030 35321030 35321030 CTCACTACAGCCTTGACCTCCTGAGCTCAAGCAGTCCTCCTGTCTCAGCCTCCCAAGTAGCTGGG CTCACTACAGCCTTGACCTCCTGAGCTCAAGCTGTCCTCCTGTCTCAGCCTCCCAAGTAGCTGGG T A AL117336.2 Ensembl:ENSG00000271335 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1366534852 Functional Loss SNV dbSNP153 33..33 33 - - - 48146 RMVar_ID_48146 Human_SNP_ID_428158077 A-to-I Human chr10 - 35323762 35323762 35323762 TGCCTTCCCTGGCCTCCGGACATGCTGGGATTACAGGTGGGAGCCACCACGCCAGGCCACAGTTT TGCCTTCCCTGGCCTCCGGACATGCTGGGATTGCAGGTGGGAGCCACCACGCCAGGCCACAGTTT T C AL117336.2 Ensembl:ENSG00000271335 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs987550139 Functional Loss SNV dbSNP153 33..33 33 - - - 48147 RMVar_ID_48147 Human_SNP_ID_428158593 A-to-I Human chr10 - 35326030 35326030 35326030 GCCCTGTTGCCTAGGTTAAAGTGCAGTGGCATAATCATGGCTCCCTGCAGCCTTGAACTCCTGGG GCCCTGTTGCCTAGGTTAAAGTGCAGTGGCATGATCATGGCTCCCTGCAGCCTTGAACTCCTGGG T C AL117336.2 Ensembl:ENSG00000271335 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1024218469 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17559263 48148 RMVar_ID_48148 Human_SNP_ID_428160725 A-to-I Human chr10 - 35335370 35335369 35335371 TGGAGGTTAACATGAGATAGAAAACTAAGTTAACACAACTCATCGACTGCCCTTGCTTTGCTTTG TGGAGGTTAACATGAGATAGAAAACTAAGTT__CACAACTCATCGACTGCCCTTGCTTTGCTTTG GTT G AL117336.2 Ensembl:ENSG00000271335 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1402704575 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_5547691,Human_RBP_ID_21913738 48149 RMVar_ID_48149 Human_SNP_ID_428160725 A-to-I Human chr10 - 35335371 35335369 35335371 TTGGAGGTTAACATGAGATAGAAAACTAAGTTAACACAACTCATCGACTGCCCTTGCTTTGCTTT TTGGAGGTTAACATGAGATAGAAAACTAAGTT__CACAACTCATCGACTGCCCTTGCTTTGCTTT GTT G AL117336.2 Ensembl:ENSG00000271335 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1402704575 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_5547691,Human_RBP_ID_21913738 48150 RMVar_ID_48150 Human_SNP_ID_428163880 A-to-I Human chr10 + 35346739 35346739 35346739 ACCTCCGCCTCCTGGGCTTAAGTGATCCTCCCACCTCAGCCTCCTGAGTAGCTGGGACTATAGTC ACCTCCGCCTCCTGGGCTTAAGTGATCCTCCCGCCTCAGCCTCCTGAGTAGCTGGGACTATAGTC A G CCNY Ensembl:ENSG00000108100 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1156534730 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_143181,RMVar_hsa_circ_80349 48151 RMVar_ID_48151 Human_SNP_ID_428165256 A-to-I Human chr10 + 35352949 35352949 35352949 CCTTTTTTCTTTCTTTCTTTCTTTTTTGAGATAGGGTCTCACTCTGTAACCTGGACTGGAGTGCA CCTTTTTTCTTTCTTTCTTTCTTTTTTGAGATGGGGTCTCACTCTGTAACCTGGACTGGAGTGCA A G CCNY Ensembl:ENSG00000108100 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1359145661 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_143181,RMVar_hsa_circ_80349 48152 RMVar_ID_48152 Human_SNP_ID_428802841 A-to-I Human chr10 - 37845142 37845142 37845142 TGGCACGTGCCTGGAGTCCCAGCTCCTCAGGAAGTTCAGGTGGAAGGATCGCTTGAGCCAGCCTC TGGCACGTGCCTGGAGTCCCAGCTCCTCAGGAGGTTCAGGTGGAAGGATCGCTTGAGCCAGCCTC T C ZNF248 Ensembl:ENSG00000198105 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1188890615 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37555,RMVar_hsa_circ_59275,RMVar_hsa_circ_72020,RMVar_hsa_circ_347727,RMVar_hsa_circ_301706,RMVar_hsa_circ_350610,RMVar_hsa_circ_8945 48153 RMVar_ID_48153 Human_SNP_ID_428831501 A-to-I Human chr10 - 37958728 37958728 37958728 TTTTTTTTTTTGATAGAGTCTTACTGTGTCTCACTGCAGCCTTAACTTCCCAGGTTCATGCGATT TTTTTTTTTTTGATAGAGTCTTACTGTGTCTCGCTGCAGCCTTAACTTCCCAGGTTCATGCGATT T C ZNF25 Ensembl:ENSG00000175395 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs549560760 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78915,RMVar_hsa_circ_66476,RMVar_hsa_circ_143210,RMVar_hsa_circ_288064 48154 RMVar_ID_48154 Human_SNP_ID_428847103 A-to-I Human chr10 + 38017289 38017288 38017290 TTGGTCCAAATCCTAAATTATTTCCTGTTAACAGGGTATTGTGTTCACAAACCAGAGGTGATCTT TTGGTCCAAATCCTAAATTATTTCCTGTTAAC__GGTATTGTGTTCACAAACCAGAGGTGATCTT CAG C ZNF33A Ensembl:ENSG00000189180 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs746303689 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_18970711 Human_Splice_Rec_1126657,Human_Splice_Rec_1126665,Human_Splice_Rec_1126671,Human_Splice_Rec_1126679,Human_Splice_Rec_1126687,Human_Splice_Rec_1126695,Human_Splice_Rec_1126711 RMVar_hsa_circ_950,RMVar_hsa_circ_284047,RMVar_hsa_circ_327478,RMVar_hsa_circ_30005,RMVar_hsa_circ_55393,RMVar_hsa_circ_366112,RMVar_hsa_circ_98558 48155 RMVar_ID_48155 Human_SNP_ID_428851495 A-to-I Human chr10 + 38035257 38035257 38035257 CTCCTGCTTCAGCTTCTCAAGTAGCCGGGACTACAGGTGCATACCACAATGCCCAGCCAATTTTT CTCCTGCTTCAGCTTCTCAAGTAGCCGGGACTGCAGGTGCATACCACAATGCCCAGCCAATTTTT A G ZNF33A Ensembl:ENSG00000189180 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1180270419 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27607459 RMVar_hsa_circ_284047,RMVar_hsa_circ_30005,RMVar_hsa_circ_55393 48156 RMVar_ID_48156 Human_SNP_ID_428858959 A-to-I Human chr10 + 38065124 38065124 38065124 AGATCATCTCGCTGCAATGTCCAGGCTGGAGTACAATGGTGCGATCTCGGCTCACTGCAACCTCC AGATCATCTCGCTGCAATGTCCAGGCTGGAGTCCAATGGTGCGATCTCGGCTCACTGCAACCTCC A C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1483430941 Functional Loss SNV dbSNP153 33..33 33 - - - 48157 RMVar_ID_48157 Human_SNP_ID_428859205 A-to-I Human chr10 + 38065951 38065951 38065951 CAGGCTGTTCTCGAACTCCTGCCTCGGCCTCCAAAAGTGCTGGGATTACCGACGTGAGCCACTGC CAGGCTGTTCTCGAACTCCTGCCTCGGCCTCCGAAAGTGCTGGGATTACCGACGTGAGCCACTGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1214756545 Functional Loss SNV dbSNP153 33..33 33 - - - 48158 RMVar_ID_48158 Human_SNP_ID_428859378 A-to-I Human chr10 + 38066663 38066663 38066663 CCACATAAAAACACTTAGTAGAGGCCAGGCACAGTGGCTCACTCCTGTAACCCCAGCACTTTGGG CCACATAAAAACACTTAGTAGAGGCCAGGCACCGTGGCTCACTCCTGTAACCCCAGCACTTTGGG A C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1433295908 Functional Loss SNV dbSNP153 33..33 33 - - - 48159 RMVar_ID_48159 Human_SNP_ID_428994553 A-to-I Human chr10 + 38577618 38577618 38577618 AATGGACACGAATGGAATAGAATGGAATGGTCACCAATGGAATGGAATGCAATGGAAAGGACTCG AATGGACACGAATGGAATAGAATGGAATGGTCCCCAATGGAATGGAATGCAATGGAAAGGACTCG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs11146698 Functional Loss SNV dbSNP153 33..33 33 - - - 48160 RMVar_ID_48160 Human_SNP_ID_428994554 A-to-I Human chr10 + 38577618 38577618 38577618 AATGGACACGAATGGAATAGAATGGAATGGTCACCAATGGAATGGAATGCAATGGAAAGGACTCG AATGGACACGAATGGAATAGAATGGAATGGTCGCCAATGGAATGGAATGCAATGGAAAGGACTCG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs11146698 Functional Loss SNV dbSNP153 33..33 33 - - - 48161 RMVar_ID_48161 Human_SNP_ID_428994555 A-to-I Human chr10 + 38577618 38577618 38577618 AATGGACACGAATGGAATAGAATGGAATGGTCACCAATGGAATGGAATGCAATGGAAAGGACTCG AATGGACACGAATGGAATAGAATGGAATGGTCTCCAATGGAATGGAATGCAATGGAAAGGACTCG A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs11146698 Functional Loss SNV dbSNP153 33..33 33 - - - 48162 RMVar_ID_48162 Human_SNP_ID_429002245 A-to-I Human chr10 + 38588659 38588659 38588659 ATTGGAATAATCATCAAATGGAATCGAATGGTATCATTGAATGGAATCAAATGGAATAATCATCA ATTGGAATAATCATCAAATGGAATCGAATGGTGTCATTGAATGGAATCAAATGGAATAATCATCA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1373911840 Functional Loss SNV dbSNP153 33..33 33 - - - 48163 RMVar_ID_48163 Human_SNP_ID_429002247 A-to-I Human chr10 + 38588671 38588661 38588671 ATCAAATGGAATCGAATGGTATCATTGAATGGAATCAAATGGAATAATCATCAGATGGAAACGAA ATCAAATGGAATCGAATGGTATC__________ATCAAATGGAATAATCATCAGATGGAAACGAA CATTGAATGGA C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1351627587 Functional Loss DEL dbSNP153 24..33 33 - - - 48164 RMVar_ID_48164 Human_SNP_ID_429002255 A-to-I Human chr10 + 38588675 38588675 38588675 AATGGAATCGAATGGTATCATTGAATGGAATCAAATGGAATAATCATCAGATGGAAACGAATGGA AATGGAATCGAATGGTATCATTGAATGGAATCGAATGGAATAATCATCAGATGGAAACGAATGGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs111208587 Functional Loss SNV dbSNP153 33..33 33 - - - 48165 RMVar_ID_48165 Human_SNP_ID_429002256 A-to-I Human chr10 + 38588675 38588675 38588675 AATGGAATCGAATGGTATCATTGAATGGAATCAAATGGAATAATCATCAGATGGAAACGAATGGA AATGGAATCGAATGGTATCATTGAATGGAATCTAATGGAATAATCATCAGATGGAAACGAATGGA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs111208587 Functional Loss SNV dbSNP153 33..33 33 - - - 48166 RMVar_ID_48166 Human_SNP_ID_429142770 A-to-I Human chr10 + 38843350 38843350 38843350 ATGGACTCGAAAGGAATGGACTCGAATGGAATAGAATACAATGGAACAGCATCGAATATAATGGA ATGGACTCGAAAGGAATGGACTCGAATGGAATGGAATACAATGGAACAGCATCGAATATAATGGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1176359374 Functional Loss SNV dbSNP153 33..33 33 - - - 48167 RMVar_ID_48167 Human_SNP_ID_429875751 A-to-I Human chr10 + 41865990 41865990 41865990 GCAGTGGAATGGAATCAACACGAGTGGAATGGAATGGAACAGAATGGAATCAACCCGAGTGGAAA GCAGTGGAATGGAATCAACACGAGTGGAATGGCATGGAACAGAATGGAATCAACCCGAGTGGAAA A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs111216910 Functional Loss SNV dbSNP153 33..33 33 - - - 48168 RMVar_ID_48168 Human_SNP_ID_429875752 A-to-I Human chr10 + 41865990 41865990 41865990 GCAGTGGAATGGAATCAACACGAGTGGAATGGAATGGAACAGAATGGAATCAACCCGAGTGGAAA GCAGTGGAATGGAATCAACACGAGTGGAATGGGATGGAACAGAATGGAATCAACCCGAGTGGAAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs111216910 Functional Loss SNV dbSNP153 33..33 33 - - - 48169 RMVar_ID_48169 Human_SNP_ID_429875754 A-to-I Human chr10 + 41865998 41865998 41865998 ATGGAATCAACACGAGTGGAATGGAATGGAACAGAATGGAATCAACCCGAGTGGAAAGTAATGGA ATGGAATCAACACGAGTGGAATGGAATGGAACGGAATGGAATCAACCCGAGTGGAAAGTAATGGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs11818702 Functional Loss SNV dbSNP153 33..33 33 - - - 48170 RMVar_ID_48170 Human_SNP_ID_429875755 A-to-I Human chr10 + 41865998 41865998 41865998 ATGGAATCAACACGAGTGGAATGGAATGGAACAGAATGGAATCAACCCGAGTGGAAAGTAATGGA ATGGAATCAACACGAGTGGAATGGAATGGAACTGAATGGAATCAACCCGAGTGGAAAGTAATGGA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs11818702 Functional Loss SNV dbSNP153 33..33 33 - - - 48171 RMVar_ID_48171 Human_SNP_ID_429884985 A-to-I Human chr10 + 41877148 41877148 41877148 ATGTAATGGAATGGATTGGAAACCACCCGATTAGAATGCAACGGAATGGAATGGAATGGAATGGA ATGTAATGGAATGGATTGGAAACCACCCGATTCGAATGCAACGGAATGGAATGGAATGGAATGGA A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs377485173 Functional Loss SNV dbSNP153 33..33 33 - - - 48172 RMVar_ID_48172 Human_SNP_ID_429884986 A-to-I Human chr10 + 41877148 41877148 41877148 ATGTAATGGAATGGATTGGAAACCACCCGATTAGAATGCAACGGAATGGAATGGAATGGAATGGA ATGTAATGGAATGGATTGGAAACCACCCGATTGGAATGCAACGGAATGGAATGGAATGGAATGGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs377485173 Functional Loss SNV dbSNP153 33..33 33 - - - 48173 RMVar_ID_48173 Human_SNP_ID_429888465 A-to-I Human chr10 + 41881377 41881373 41881378 ATGAAATCAACCCGATTGGAATGGAATGGAATACAATGGAATGGAATGGAATCAACTGGAAAGGA ATGAAATCAACCCGATTGGAATGGAATGG_____AATGGAATGGAATGGAATCAACTGGAAAGGA GAATAC G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1439447108 Functional Loss DEL dbSNP153 30..34 33 - - - 48174 RMVar_ID_48174 Human_SNP_ID_429888467 A-to-I Human chr10 + 41881377 41881377 41881377 ATGAAATCAACCCGATTGGAATGGAATGGAATACAATGGAATGGAATGGAATCAACTGGAAAGGA ATGAAATCAACCCGATTGGAATGGAATGGAATCCAATGGAATGGAATGGAATCAACTGGAAAGGA A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs62646705 Functional Loss SNV dbSNP153 33..33 33 - - - 48175 RMVar_ID_48175 Human_SNP_ID_429888468 A-to-I Human chr10 + 41881377 41881377 41881377 ATGAAATCAACCCGATTGGAATGGAATGGAATACAATGGAATGGAATGGAATCAACTGGAAAGGA ATGAAATCAACCCGATTGGAATGGAATGGAATGCAATGGAATGGAATGGAATCAACTGGAAAGGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs62646705 Functional Loss SNV dbSNP153 33..33 33 - - - 48176 RMVar_ID_48176 Human_SNP_ID_429889160 A-to-I Human chr10 + 41882413 41882413 41882413 TGCTACGGAATCAACCTGAGTGGAATGGAAATAAATGGACTGGAACGGTATGGAATGGAATGGAT TGCTACGGAATCAACCTGAGTGGAATGGAAATGAATGGACTGGAACGGTATGGAATGGAATGGAT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs796695004 Functional Loss SNV dbSNP153 33..33 33 - - - 48177 RMVar_ID_48177 Human_SNP_ID_429889254 A-to-I Human chr10 + 41882677 41882677 41882677 ATGGAATGGAATCAACCAAAGTGTAATGGAATAGAATGGATGCAACGGAATCAAACCAGTGGAAT ATGGAATGGAATCAACCAAAGTGTAATGGAATGGAATGGATGCAACGGAATCAAACCAGTGGAAT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs74790593 Functional Loss SNV dbSNP153 33..33 33 - - - 48178 RMVar_ID_48178 Human_SNP_ID_429928966 A-to-I Human chr10 + 42104155 42104155 42104155 ATCATTGAACGGAATCGAATGGAATCATCATCAGATGGAAACGAATGGAATCATCATCGAATGGA ATCATTGAACGGAATCGAATGGAATCATCATCCGATGGAAACGAATGGAATCATCATCGAATGGA A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs148121689 Functional Loss SNV dbSNP153 33..33 33 - - - 48179 RMVar_ID_48179 Human_SNP_ID_429928967 A-to-I Human chr10 + 42104155 42104155 42104155 ATCATTGAACGGAATCGAATGGAATCATCATCAGATGGAAACGAATGGAATCATCATCGAATGGA ATCATTGAACGGAATCGAATGGAATCATCATCGGATGGAAACGAATGGAATCATCATCGAATGGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs148121689 Functional Loss SNV dbSNP153 33..33 33 - - - 48180 RMVar_ID_48180 Human_SNP_ID_429929007 A-to-I Human chr10 + 42104187 42104187 42104187 AGATGGAAACGAATGGAATCATCATCGAATGGAAATGAAAGGAGTCATCATCTAATGGAATCGCA AGATGGAAACGAATGGAATCATCATCGAATGGCAATGAAAGGAGTCATCATCTAATGGAATCGCA A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs151335338 Functional Loss SNV dbSNP153 33..33 33 - - - 48181 RMVar_ID_48181 Human_SNP_ID_430006522 A-to-I Human chr10 - 42296911 42296901 42296911 ATGCAATGAAAAGGAACGGACTCGAATGGAATAGAATGGAATGGAATGTCCCGAAAGGAGGGGAA ATGCAATGAAAAGGAACGGACTCGAATGGAAT__________GGAATGTCCCGAAAGGAGGGGAA CATTCCATTCT C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs766065348 Functional Loss DEL dbSNP153 33..42 33 - - - 48182 RMVar_ID_48182 Human_SNP_ID_430073860 A-to-I Human chr10 - 42518071 42518071 42518071 AAATAGGCTGAGCATGGTGGCTTGCACCTGTAATCCCAGTACTTTGGGAGGTTGAGGTGGGCAAG AAATAGGCTGAGCATGGTGGCTTGCACCTGTAGTCCCAGTACTTTGGGAGGTTGAGGTGGGCAAG T C ZNF37BP Ensembl:ENSG00000234420 Pseudogene exon GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1415561952 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17346900,Human_RBP_ID_18510459 48183 RMVar_ID_48183 Human_SNP_ID_430073867 A-to-I Human chr10 - 42518090 42518090 42518090 TGGGGCTTTGAAAAAGCACAAATAGGCTGAGCATGGTGGCTTGCACCTGTAATCCCAGTACTTTG TGGGGCTTTGAAAAAGCACAAATAGGCTGAGCTTGGTGGCTTGCACCTGTAATCCCAGTACTTTG T A ZNF37BP Ensembl:ENSG00000234420 Pseudogene exon GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1385480829 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17346900 48184 RMVar_ID_48184 Human_SNP_ID_430091381 A-to-I Human chr10 - 42580416 42580416 42580416 CTGGCCAACATGGCAAAACCCCATCTCTACTAAAAATACAAAAATTAGCCAGATGTGGCACATAC CTGGCCAACATGGCAAAACCCCATCTCTACTAGAAATACAAAAATTAGCCAGATGTGGCACATAC T C ZNF33B Ensembl:ENSG00000196693 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1298425970 Functional Loss SNV dbSNP153 33..33 33 - - - 48185 RMVar_ID_48185 Human_SNP_ID_430099640 A-to-I Human chr10 - 42613325 42613309 42613326 CAGGCTGGTCACGAACTCCTGATCTTTTAGGTAGTCCACCCACCTCGGCCTCCCAAAGTGCTGGG CAGGCTGGTCACGAACTCCTGATCTTTTAGG_________________CCTCCCAAAGTGCTGGG GCCGAGGTGGGTGGACTA G ZNF33B Ensembl:ENSG00000196693 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1266315942 Functional Loss DEL dbSNP153 32..48 33 - - - RMVar_hsa_circ_38549,RMVar_hsa_circ_56025 48186 RMVar_ID_48186 Human_SNP_ID_430103218 A-to-I Human chr10 - 42628311 42628311 42628311 AGCATCATTATAGAATAGTGCTCAACAAGGCCAGGTGCGGTGTCTCACGCCTGTAATTCCAGCAC AGCATCATTATAGAATAGTGCTCAACAAGGCCGGGTGCGGTGTCTCACGCCTGTAATTCCAGCAC T C ZNF33B Ensembl:ENSG00000196693 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs371796352 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22565826 RMVar_hsa_circ_38549,RMVar_hsa_circ_56025,RMVar_hsa_circ_52373 48187 RMVar_ID_48187 Human_SNP_ID_430116408 A-to-I Human chr10 - 42674289 42674289 42674289 ACCATCTTGGCTCATTGCAACATCTGGCTCCCAGGTTCAATCGATTCTTCTGCCTCAGCCTTCTG ACCATCTTGGCTCATTGCAACATCTGGCTCCCCGGTTCAATCGATTCTTCTGCCTCAGCCTTCTG T G LINC01518 Ensembl:ENSG00000233515 lincRNA intron GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs1261522647 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1127164,Human_Splice_Rec_1127172 RMVar_hsa_circ_110955,RMVar_hsa_circ_114431,RMVar_hsa_circ_112822,RMVar_hsa_circ_143228,RMVar_hsa_circ_143230,RMVar_hsa_circ_107355,RMVar_hsa_circ_143229,RMVar_hsa_circ_143227 48188 RMVar_ID_48188 Human_SNP_ID_430153609 A-to-I Human chr10 + 42820931 42820931 42820931 GTTCGCTATATTTCTTTTTTTCCTTTTCCTTTAAGGCCCTATCACTCCACAGGGAACTGGTTTCT GTTCGCTATATTTCTTTTTTTCCTTTTCCTTTGAGGCCCTATCACTCCACAGGGAACTGGTTTCT A G BMS1 Ensembl:ENSG00000165733 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs930691232 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_861159,Human_RBP_ID_5339876,Human_RBP_ID_5971853,Human_RBP_ID_8334535,Human_RBP_ID_19517313,Human_RBP_ID_24556753,Human_RBP_ID_24811945 Human_Splice_Rec_1127237 RMVar_hsa_circ_638,RMVar_hsa_circ_143231,RMVar_hsa_circ_79134,RMVar_hsa_circ_83573,RMVar_hsa_circ_85213,RMVar_hsa_circ_143234,RMVar_hsa_circ_143235,RMVar_hsa_circ_70322,RMVar_hsa_circ_334722,RMVar_hsa_circ_143243,RMVar_hsa_circ_268143 48189 RMVar_ID_48189 Human_SNP_ID_430301846 A-to-I Human chr10 - 43398208 43398208 43398208 CAGCCTAGCCAACACGGTGAAACCACATCTCTACTAAAAACAAAAACTAGCTGGGTATAGTGGCA CAGCCTAGCCAACACGGTGAAACCACATCTCTGCTAAAAACAAAAACTAGCTGGGTATAGTGGCA T C HNRNPF Ensembl:ENSG00000169813 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1321988834 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17777530 RMVar_hsa_circ_85905,RMVar_hsa_circ_143275,RMVar_hsa_circ_92092,RMVar_hsa_circ_143278 48190 RMVar_ID_48190 Human_SNP_ID_430301942 A-to-I Human chr10 - 43398409 43398409 43398409 TTGAACCTGGGAGGGGAGGTTGCAGTGAGCCGAGATCGTGCCATTGCACTCCAGCCCGGGCAACA TTGAACCTGGGAGGGGAGGTTGCAGTGAGCCGCGATCGTGCCATTGCACTCCAGCCCGGGCAACA T G HNRNPF Ensembl:ENSG00000169813 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs548781989 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85905,RMVar_hsa_circ_143275,RMVar_hsa_circ_92092,RMVar_hsa_circ_143278 48191 RMVar_ID_48191 Human_SNP_ID_430302183 A-to-I Human chr10 - 43399287 43399287 43399287 GCCCAGGAGTTACAGACCAGTCTGGGCATCATAGAGAGACCTTGCCTCTACTAAAAAATTAAAAA GCCCAGGAGTTACAGACCAGTCTGGGCATCATGGAGAGACCTTGCCTCTACTAAAAAATTAAAAA T C HNRNPF Ensembl:ENSG00000169813 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1564397973 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85905,RMVar_hsa_circ_143275,RMVar_hsa_circ_92092,RMVar_hsa_circ_143278 48192 RMVar_ID_48192 Human_SNP_ID_430302629 A-to-I Human chr10 - 43400934 43400934 43400934 GGGACTACAGGTGCCTGCCACCACGTTTGGCTAATTTTTGTATTTTTAGTAGAGACGAGGTTTCA GGGACTACAGGTGCCTGCCACCACGTTTGGCTGATTTTTGTATTTTTAGTAGAGACGAGGTTTCA T C HNRNPF Ensembl:ENSG00000169813 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs967460105 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85905,RMVar_hsa_circ_143275,RMVar_hsa_circ_92092,RMVar_hsa_circ_143278 48193 RMVar_ID_48193 Human_SNP_ID_430302630 A-to-I Human chr10 - 43400934 43400934 43400934 GGGACTACAGGTGCCTGCCACCACGTTTGGCTAATTTTTGTATTTTTAGTAGAGACGAGGTTTCA GGGACTACAGGTGCCTGCCACCACGTTTGGCTCATTTTTGTATTTTTAGTAGAGACGAGGTTTCA T G HNRNPF Ensembl:ENSG00000169813 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs967460105 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85905,RMVar_hsa_circ_143275,RMVar_hsa_circ_92092,RMVar_hsa_circ_143278 48194 RMVar_ID_48194 Human_SNP_ID_430308718 A-to-I Human chr10 + 43420900 43420900 43420900 GGCTCAAGCGATCCGCCCGCCTGGGCCTCCCAAAGTGCTGAGACTGCAGGCATGAGCCACCGCGC GGCTCAAGCGATCCGCCCGCCTGGGCCTCCCAGAGTGCTGAGACTGCAGGCATGAGCCACCGCGC A G AL450326.1 Ensembl:ENSG00000230555 lincRNA exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1217066924 Functional Loss SNV dbSNP153 33..33 33 - - - 48195 RMVar_ID_48195 Human_SNP_ID_430308961 A-to-I Human chr10 + 43421849 43421849 43421849 AGCTGGGCTTGGTGGCTCACGCCTGTAATCCCAGCACTTTGTGAAGCCAAGGCGGGAGCATCGAT AGCTGGGCTTGGTGGCTCACGCCTGTAATCCCGGCACTTTGTGAAGCCAAGGCGGGAGCATCGAT A G AL450326.1 Ensembl:ENSG00000230555 lincRNA exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1321898016 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_3168721,Human_miRNA_ID_3180335 48196 RMVar_ID_48196 Human_SNP_ID_430308966 A-to-I Human chr10 + 43421860 43421860 43421860 GTGGCTCACGCCTGTAATCCCAGCACTTTGTGAAGCCAAGGCGGGAGCATCGATTGAGCCTAGCA GTGGCTCACGCCTGTAATCCCAGCACTTTGTGGAGCCAAGGCGGGAGCATCGATTGAGCCTAGCA A G AL450326.1 Ensembl:ENSG00000230555 lincRNA exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1397941635 Functional Loss SNV dbSNP153 33..33 33 - - - 48197 RMVar_ID_48197 Human_SNP_ID_430309111 A-to-I Human chr10 + 43422274 43422274 43422274 GGCGGATCACTTGAGGCCAGGAGTTCCAGACCAGCCTGGCTAACATGGCAAAACCCTGTCTCTAC GGCGGATCACTTGAGGCCAGGAGTTCCAGACCGGCCTGGCTAACATGGCAAAACCCTGTCTCTAC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1403456286 Functional Loss SNV dbSNP153 33..33 33 - - - 48198 RMVar_ID_48198 Human_SNP_ID_430309133 A-to-I Human chr10 + 43422340 43422340 43422340 AAAAAATACAAAAATTAGCCTGGTATGGTGGCACACGCCTGTAATCCCTGCTACTCCGGAGGCTG AAAAAATACAAAAATTAGCCTGGTATGGTGGCGCACGCCTGTAATCCCTGCTACTCCGGAGGCTG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs528393059 Functional Loss SNV dbSNP153 33..33 33 - - - 48199 RMVar_ID_48199 Human_SNP_ID_430309137 A-to-I Human chr10 + 43422350 43422350 43422350 AAAATTAGCCTGGTATGGTGGCACACGCCTGTAATCCCTGCTACTCCGGAGGCTGAGGAATGAGA AAAATTAGCCTGGTATGGTGGCACACGCCTGTGATCCCTGCTACTCCGGAGGCTGAGGAATGAGA A G - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs936619584 Functional Loss SNV dbSNP153 33..33 33 - - - 48200 RMVar_ID_48200 Human_SNP_ID_430312815 A-to-I Human chr10 - 43435338 43435338 43435338 CCCAGTTATTCGGGAGGCTGAGGCAGGAGAATAGCTTGCACCCGGGAGGCAGAGGTTGCTGTGAG CCCAGTTATTCGGGAGGCTGAGGCAGGAGAATTGCTTGCACCCGGGAGGCAGAGGTTGCTGTGAG T A 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,intron,exon,exon,exon,exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs540749383 Functional Loss SNV dbSNP153 33..33 33 - - - 48201 RMVar_ID_48201 Human_SNP_ID_430312816 A-to-I Human chr10 - 43435338 43435338 43435338 CCCAGTTATTCGGGAGGCTGAGGCAGGAGAATAGCTTGCACCCGGGAGGCAGAGGTTGCTGTGAG CCCAGTTATTCGGGAGGCTGAGGCAGGAGAATGGCTTGCACCCGGGAGGCAGAGGTTGCTGTGAG 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,intron,exon,exon,exon,exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs540749383 Functional Loss SNV dbSNP153 33..33 33 - - - 48202 RMVar_ID_48202 Human_SNP_ID_430312843 A-to-I Human chr10 - 43435453 43435453 43435453 AAGGCGGGTGGATCACCTGAGATCAGGAGTTTAAGATCAGTCTGGCCTACATGGTGAAACTCCAA AAGGCGGGTGGATCACCTGAGATCAGGAGTTTGAGATCAGTCTGGCCTACATGGTGAAACTCCAA 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,intron,exon,exon,exon,exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1422378318 Functional Loss SNV dbSNP153 33..33 33 - - - 48203 RMVar_ID_48203 Human_SNP_ID_430356516 A-to-I Human chr10 + 43605134 43605134 43605134 TCCACAATGCCCACCATATCATCGAATACCAGACCAAGTTTCTTACAATTATCTACTGTAATGGA TCCACAATGCCCACCATATCATCGAATACCAGGCCAAGTTTCTTACAATTATCTACTGTAATGGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1171331738 Functional Loss SNV dbSNP153 33..33 33 - - - 48204 RMVar_ID_48204 Human_SNP_ID_430361181 A-to-I Human chr10 + 43625165 43625165 43625165 TAGAAATGGGGTCTCCCTATGTTGATCAGGCTAGTCTTGAACTCCTGGGCTCAAGCAATCCTCTT TAGAAATGGGGTCTCCCTATGTTGATCAGGCTGGTCTTGAACTCCTGGGCTCAAGCAATCCTCTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1429145188 Functional Loss SNV dbSNP153 33..33 33 - - - 48205 RMVar_ID_48205 Human_SNP_ID_583328354 A-to-I Human chr15 + 75007411 75007411 75007411 TTGTTTGCAGTTTCTTTTTCTTTTTTTGAGACAGGGTCTTGCTCTGCCGCCCGGGCTGGAGTGCA TTGTTTGCAGTTTCTTTTTCTTTTTTTGAGACGGGGTCTTGCTCTGCCGCCCGGGCTGGAGTGCA A G SCAMP5 Ensembl:ENSG00000198794 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1414148499 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118062,RMVar_hsa_circ_173922 48206 RMVar_ID_48206 Human_SNP_ID_583328355 A-to-I Human chr15 + 75007411 75007411 75007411 TTGTTTGCAGTTTCTTTTTCTTTTTTTGAGACAGGGTCTTGCTCTGCCGCCCGGGCTGGAGTGCA TTGTTTGCAGTTTCTTTTTCTTTTTTTGAGACTGGGTCTTGCTCTGCCGCCCGGGCTGGAGTGCA A T SCAMP5 Ensembl:ENSG00000198794 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1414148499 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118062,RMVar_hsa_circ_173922 48207 RMVar_ID_48207 Human_SNP_ID_583335542 A-to-I Human chr15 + 75036858 75036857 75036858 GATGATTGATTGATTATTTTTTTTTTGTAGAGAAGGAGTTTTGCCCTGTTGCCCAGGCTCATCCC GATGATTGATTGATTATTTTTTTTTTGTAGAG_AGGAGTTTTGCCCTGTTGCCCAGGCTCATCCC GA G PPCDC Ensembl:ENSG00000138621 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs963461256 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_12592652,Human_RBP_ID_22931703 48208 RMVar_ID_48208 Human_SNP_ID_583339002 A-to-I Human chr15 + 75051062 75051062 75051062 CACCACGCCCAGCTTATTTTTGTATTATTTGTAGAGATGGGTTTTGCCATGTTGGCCAGACTAAT CACCACGCCCAGCTTATTTTTGTATTATTTGTGGAGATGGGTTTTGCCATGTTGGCCAGACTAAT A G PPCDC Ensembl:ENSG00000138621 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs976576406 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12592819 48209 RMVar_ID_48209 Human_SNP_ID_583340033 A-to-I Human chr15 + 75054982 75054982 75054982 TTAGTTTAAGACCAGAAGTTTGAGACAGGCCTAGGCAACACAGTGAGACTCCATCTCTACCAAAA TTAGTTTAAGACCAGAAGTTTGAGACAGGCCTGGGCAACACAGTGAGACTCCATCTCTACCAAAA A G PPCDC Ensembl:ENSG00000138621 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs923738410 Functional Loss SNV dbSNP153 33..33 33 - - - 48210 RMVar_ID_48210 Human_SNP_ID_583390903 A-to-I Human chr15 + 75272219 75272219 75272219 ATTAGATAAACTCAGTTCCAGAATTATAAAGAAAAACTGTTAGACCAACGAATGTGGCTAATTAA ATTAGATAAACTCAGTTCCAGAATTATAAAGAGAAACTGTTAGACCAACGAATGTGGCTAATTAA A G - - Other Unknown GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1190276191 Functional Loss SNV dbSNP153 33..33 33 - - - 48211 RMVar_ID_48211 Human_SNP_ID_583407845 A-to-I Human chr15 + 75341941 75341941 75341941 AAAAAATTAGCCGATCATGGTGGTGCGTGCTTATAGTCTCAGCTACTCAGAAGGCTGAGGCAGGA AAAAAATTAGCCGATCATGGTGGTGCGTGCTTGTAGTCTCAGCTACTCAGAAGGCTGAGGCAGGA A G COMMD4 Ensembl:ENSG00000140365 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1011116295 Functional Loss SNV dbSNP153 33..33 33 - - - 48212 RMVar_ID_48212 Human_SNP_ID_583407846 A-to-I Human chr15 + 75341943 75341943 75341943 AAAATTAGCCGATCATGGTGGTGCGTGCTTATAGTCTCAGCTACTCAGAAGGCTGAGGCAGGAGG AAAATTAGCCGATCATGGTGGTGCGTGCTTATGGTCTCAGCTACTCAGAAGGCTGAGGCAGGAGG A G COMMD4 Ensembl:ENSG00000140365 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1022986564 Functional Loss SNV dbSNP153 33..33 33 - - - 48213 RMVar_ID_48213 Human_SNP_ID_583408022 A-to-I Human chr15 + 75342520 75342520 75342520 TGATAGTGCCCCTGCACTCCAGCCTGGGTGACAGTGAGACCCTGTCTCAAAAAAAAAAAGTTAAA TGATAGTGCCCCTGCACTCCAGCCTGGGTGACGGTGAGACCCTGTCTCAAAAAAAAAAAGTTAAA A G COMMD4 Ensembl:ENSG00000140365 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1298566633 Functional Loss SNV dbSNP153 33..33 33 - - - 48214 RMVar_ID_48214 Human_SNP_ID_583408558 A-to-I Human chr15 + 75344699 75344699 75344699 CACATTTTTTTTAGGGGGGCAGGGATGGGGATAAGGTTTCACTCTGTCATCCAGGCTAGAGTGCA CACATTTTTTTTAGGGGGGCAGGGATGGGGATGAGGTTTCACTCTGTCATCCAGGCTAGAGTGCA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973231424 Functional Loss SNV dbSNP153 33..33 33 - - - 48215 RMVar_ID_48215 Human_SNP_ID_583408564 A-to-I Human chr15 + 75344724 75344724 75344724 TGGGGATAAGGTTTCACTCTGTCATCCAGGCTAGAGTGCAGCAGCATGATCACAGTTCACTGTAG TGGGGATAAGGTTTCACTCTGTCATCCAGGCTGGAGTGCAGCAGCATGATCACAGTTCACTGTAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs937368434 Functional Loss SNV dbSNP153 33..33 33 - - - 48216 RMVar_ID_48216 Human_SNP_ID_583410529 A-to-I Human chr15 + 75351324 75351324 75351324 TTGAGACAGGGTCTCGCTCTGTTGCCTAGGCTAGAGTACAGTGGCGCCATCACAGCTCATTGCAG TTGAGACAGGGTCTCGCTCTGTTGCCTAGGCTGGAGTACAGTGGCGCCATCACAGCTCATTGCAG A G NEIL1 Ensembl:ENSG00000140398 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1361502435 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1628068,Human_Splice_Rec_1628069 48217 RMVar_ID_48217 Human_SNP_ID_583411285 A-to-I Human chr15 + 75353374 75353374 75353374 CCTCTAAGTAGCTAGGACTACAGGCTCACACCACCACACCGGGCTAATTGTTAAAAATTTTTTTT CCTCTAAGTAGCTAGGACTACAGGCTCACACCGCCACACCGGGCTAATTGTTAAAAATTTTTTTT A G NEIL1 Ensembl:ENSG00000140398 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1467270639 Functional Loss SNV dbSNP153 33..33 33 - - - 48218 RMVar_ID_48218 Human_SNP_ID_583411320 A-to-I Human chr15 + 75353477 75353477 75353477 TGAACTCCTGGCCCCTAGGGATTCTCCCATCTAAGCTTCCCAAAGTGTCGGGATTACAGGTGTGG TGAACTCCTGGCCCCTAGGGATTCTCCCATCTGAGCTTCCCAAAGTGTCGGGATTACAGGTGTGG A G NEIL1 Ensembl:ENSG00000140398 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs556550650 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5179017 48219 RMVar_ID_48219 Human_SNP_ID_583411397 A-to-I Human chr15 + 75353665 75353665 75353665 GTCCATCAGCTTGTGTAGCTGAGGTCTGGGCCAGGTCTAACCAGGCTCCCCACTCCTCCCAACCT GTCCATCAGCTTGTGTAGCTGAGGTCTGGGCCGGGTCTAACCAGGCTCCCCACTCCTCCCAACCT A G NEIL1 Ensembl:ENSG00000140398 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs757012135 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26757009 48220 RMVar_ID_48220 Human_SNP_ID_583411398 A-to-I Human chr15 + 75353665 75353665 75353665 GTCCATCAGCTTGTGTAGCTGAGGTCTGGGCCAGGTCTAACCAGGCTCCCCACTCCTCCCAACCT GTCCATCAGCTTGTGTAGCTGAGGTCTGGGCCTGGTCTAACCAGGCTCCCCACTCCTCCCAACCT A T NEIL1 Ensembl:ENSG00000140398 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs757012135 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26757009 48221 RMVar_ID_48221 Human_SNP_ID_583413495 A-to-I Human chr15 - 75359178 75359178 75359178 AGACTTTTGGTGTGGGAAGCCCCTACAGACTCAGCCTCAAGGCCTCCTCCCACAAAGACTGATGG AGACTTTTGGTGTGGGAAGCCCCTACAGACTCGGCCTCAAGGCCTCCTCCCACAAAGACTGATGG T C MAN2C1 Ensembl:ENSG00000140400 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs372282957 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_758998,Human_RBP_ID_815302,Human_RBP_ID_886434,Human_RBP_ID_3945728,Human_RBP_ID_5141424,Human_RBP_ID_5179538,Human_RBP_ID_5354592,Human_RBP_ID_8422910,Human_RBP_ID_9418788,Human_RBP_ID_18418601,Human_RBP_ID_18981691,Human_RBP_ID_19067468,Human_RBP_ID_21969961,Human_RBP_ID_22047592,Human_RBP_ID_22473430,Human_RBP_ID_22650141,Human_RBP_ID_22737838,Human_RBP_ID_25183924,Human_RBP_ID_27837458 Human_Splice_Rec_1628250 RMVar_hsa_circ_86117,RMVar_hsa_circ_90887,RMVar_hsa_circ_173932,RMVar_hsa_circ_110230,RMVar_hsa_circ_173934,RMVar_hsa_circ_80789,RMVar_hsa_circ_173935,RMVar_hsa_circ_173933 48222 RMVar_ID_48222 Human_SNP_ID_583419448 A-to-I Human chr15 - 75379179 75379179 75379179 AAATAACAATATTGGGCTGGGCGCAGTGGCTCACGCCTGTAACTCCAGCACTTTGGGAGGCCGAG AAATAACAATATTGGGCTGGGCGCAGTGGCTCGCGCCTGTAACTCCAGCACTTTGGGAGGCCGAG T C SIN3A Ensembl:ENSG00000169375 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1311723151 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268935,RMVar_hsa_circ_348133,RMVar_hsa_circ_330989 48223 RMVar_ID_48223 Human_SNP_ID_583420623 A-to-I Human chr15 - 75383760 75383760 75383760 AAAATTAGCCCGGCATGGTAGCGTGCACCTGTAGTCTCAGCTACTCAGGAGAATGAGGTAGAAGG AAAATTAGCCCGGCATGGTAGCGTGCACCTGTCGTCTCAGCTACTCAGGAGAATGAGGTAGAAGG T G SIN3A Ensembl:ENSG00000169375 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs551981642 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_356305,RMVar_hsa_circ_268935,RMVar_hsa_circ_348133,RMVar_hsa_circ_372775,RMVar_hsa_circ_374109,RMVar_hsa_circ_306412,RMVar_hsa_circ_337205,RMVar_hsa_circ_94951,RMVar_hsa_circ_127925,RMVar_hsa_circ_173940,RMVar_hsa_circ_173941,RMVar_hsa_circ_173942,RMVar_hsa_circ_173939,RMVar_hsa_circ_173943,RMVar_hsa_circ_60899 48224 RMVar_ID_48224 Human_SNP_ID_583420630 A-to-I Human chr15 - 75383773 75383773 75383773 ATACAAGAATACAAAAATTAGCCCGGCATGGTAGCGTGCACCTGTAGTCTCAGCTACTCAGGAGA ATACAAGAATACAAAAATTAGCCCGGCATGGTGGCGTGCACCTGTAGTCTCAGCTACTCAGGAGA T C SIN3A Ensembl:ENSG00000169375 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1214774402 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_356305,RMVar_hsa_circ_268935,RMVar_hsa_circ_348133,RMVar_hsa_circ_372775,RMVar_hsa_circ_374109,RMVar_hsa_circ_306412,RMVar_hsa_circ_337205,RMVar_hsa_circ_94951,RMVar_hsa_circ_127925,RMVar_hsa_circ_173940,RMVar_hsa_circ_173941,RMVar_hsa_circ_173942,RMVar_hsa_circ_173939,RMVar_hsa_circ_173943,RMVar_hsa_circ_60899 48225 RMVar_ID_48225 Human_SNP_ID_583425160 A-to-I Human chr15 - 75402147 75402147 75402147 ATGACCTCGTCTCTGCAAAAAATTTAGAAATTAGCCAGGCATGGTGGCTCACACCTGTAGTCCCA ATGACCTCGTCTCTGCAAAAAATTTAGAAATTTGCCAGGCATGGTGGCTCACACCTGTAGTCCCA T A SIN3A Ensembl:ENSG00000169375 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1054889509 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37540,RMVar_hsa_circ_356305,RMVar_hsa_circ_268935,RMVar_hsa_circ_94951,RMVar_hsa_circ_127925,RMVar_hsa_circ_173941,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_39204,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_34476,RMVar_hsa_circ_173953,RMVar_hsa_circ_173954,RMVar_hsa_circ_32888 48226 RMVar_ID_48226 Human_SNP_ID_583427405 A-to-I Human chr15 - 75410524 75410524 75410524 GCCGAGACAAGTGCACTCCAGCCTGAGCAACAAGAGTGAAACTCCGTCTCAAAAATATTTACTAC GCCGAGACAAGTGCACTCCAGCCTGAGCAACAGGAGTGAAACTCCGTCTCAAAAATATTTACTAC T C SIN3A Ensembl:ENSG00000169375 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs953089442 Functional Loss SNV dbSNP153 33..33 33 - - - 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_173957 48227 RMVar_ID_48227 Human_SNP_ID_583430694 A-to-I Human chr15 - 75423247 75423247 75423247 TTTAGAGACGGTCTCATTCTGTCACCTGGGCTAGAGAGCAGTGGTGTGATCACAGCTCACTGCAG TTTAGAGACGGTCTCATTCTGTCACCTGGGCTGGAGAGCAGTGGTGTGATCACAGCTCACTGCAG T C SIN3A Ensembl:ENSG00000169375 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1174527030 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12594404 RMVar_hsa_circ_356305,RMVar_hsa_circ_173942,RMVar_hsa_circ_109789,RMVar_hsa_circ_173951,RMVar_hsa_circ_361143,RMVar_hsa_circ_37513,RMVar_hsa_circ_173956,RMVar_hsa_circ_271971,RMVar_hsa_circ_173964 48228 RMVar_ID_48228 Human_SNP_ID_583430782 A-to-I Human chr15 - 75423514 75423514 75423514 GCCAACACGCCTGGTTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGCTAGCCAGGA GCCAACACGCCTGGTTAATTTTTTGTATTTTTGGTAGAGACGGGGTTTCACCATGCTAGCCAGGA T C SIN3A Ensembl:ENSG00000169375 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs896113578 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_356305,RMVar_hsa_circ_173942,RMVar_hsa_circ_109789,RMVar_hsa_circ_173951,RMVar_hsa_circ_361143,RMVar_hsa_circ_37513,RMVar_hsa_circ_173956,RMVar_hsa_circ_271971,RMVar_hsa_circ_173964 48229 RMVar_ID_48229 Human_SNP_ID_583431547 A-to-I Human chr15 - 75426679 75426679 75426679 GTGATCTGCCCGACTCGGCCTCCCAAACTGCTAGGATTACAGGCATGAGCCACCTCGTCCGCCCT GTGATCTGCCCGACTCGGCCTCCCAAACTGCTGGGATTACAGGCATGAGCCACCTCGTCCGCCCT T C SIN3A Ensembl:ENSG00000169375 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1408669281 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_356305,RMVar_hsa_circ_173942,RMVar_hsa_circ_109789,RMVar_hsa_circ_173951,RMVar_hsa_circ_361143,RMVar_hsa_circ_37513,RMVar_hsa_circ_173956,RMVar_hsa_circ_271971,RMVar_hsa_circ_173964 48230 RMVar_ID_48230 Human_SNP_ID_583432083 A-to-I Human chr15 - 75428468 75428468 75428468 TTGAAAAAATAAATAAAAAATTAGCCAGGCATAGTGGTGTGCATCTGTAGTCCTAGCTACCCGGG TTGAAAAAATAAATAAAAAATTAGCCAGGCATGGTGGTGTGCATCTGTAGTCCTAGCTACCCGGG T C SIN3A Ensembl:ENSG00000169375 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982089215 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17563290 RMVar_hsa_circ_356305,RMVar_hsa_circ_173942,RMVar_hsa_circ_109789,RMVar_hsa_circ_173951,RMVar_hsa_circ_361143,RMVar_hsa_circ_37513,RMVar_hsa_circ_173956,RMVar_hsa_circ_271971,RMVar_hsa_circ_173964 48231 RMVar_ID_48231 Human_SNP_ID_583435223 A-to-I Human chr15 - 75440029 75440029 75440029 CTCCTGCCTCAGCCTCCAAAGTTGCTGGGATTACAGGCGCCCGCTACCACGCCCAGCTAATTTTT CTCCTGCCTCAGCCTCCAAAGTTGCTGGGATTGCAGGCGCCCGCTACCACGCCCAGCTAATTTTT T C SIN3A Ensembl:ENSG00000169375 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1002590753 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_276960 48232 RMVar_ID_48232 Human_SNP_ID_583445198 A-to-I Human chr15 - 75476538 75476538 75476538 GGCCAAGGCGGGCAGATCACTTGAGGTCAGGTATTTGAAACCAGCCTGGCCAACATGATGAAACC GGCCAAGGCGGGCAGATCACTTGAGGTCAGGTTTTTGAAACCAGCCTGGCCAACATGATGAAACC T A PTPN9 Ensembl:ENSG00000169410 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs969388932 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43141,RMVar_hsa_circ_377333,RMVar_hsa_circ_338779,RMVar_hsa_circ_173968,RMVar_hsa_circ_47194,RMVar_hsa_circ_331407,RMVar_hsa_circ_109145,RMVar_hsa_circ_304866,RMVar_hsa_circ_173967,RMVar_hsa_circ_341102,RMVar_hsa_circ_284944,RMVar_hsa_circ_173971 48233 RMVar_ID_48233 Human_SNP_ID_583451467 A-to-I Human chr15 - 75500861 75500861 75500861 TTTTTTAGAGACAGGGTCTTGCTCTGTCCCCCAGACTGGCGCATAGTGGCATGATCATGGCTCAC TTTTTTAGAGACAGGGTCTTGCTCTGTCCCCCCGACTGGCGCATAGTGGCATGATCATGGCTCAC T G PTPN9 Ensembl:ENSG00000169410 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1034479336 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_173973,RMVar_hsa_circ_43141,RMVar_hsa_circ_377333,RMVar_hsa_circ_338779,RMVar_hsa_circ_4406,RMVar_hsa_circ_109145,RMVar_hsa_circ_173967,RMVar_hsa_circ_341102,RMVar_hsa_circ_173971,RMVar_hsa_circ_47658,RMVar_hsa_circ_14009,RMVar_hsa_circ_271902,RMVar_hsa_circ_332360,RMVar_hsa_circ_268651,RMVar_hsa_circ_173974 48234 RMVar_ID_48234 Human_SNP_ID_583456739 A-to-I Human chr15 - 75519894 75519894 75519894 GAACTTCTGGCCTCAAGCAGTCTTCACATCTCAGTCTCCCAAAGTGCTGAGATTACAGGTGTGAG GAACTTCTGGCCTCAAGCAGTCTTCACATCTCGGTCTCCCAAAGTGCTGAGATTACAGGTGTGAG T C PTPN9 Ensembl:ENSG00000169410 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1400469306 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_173973,RMVar_hsa_circ_338779,RMVar_hsa_circ_109145,RMVar_hsa_circ_173967,RMVar_hsa_circ_341102,RMVar_hsa_circ_173971,RMVar_hsa_circ_47658,RMVar_hsa_circ_271902,RMVar_hsa_circ_332360,RMVar_hsa_circ_173974,RMVar_hsa_circ_173977,RMVar_hsa_circ_173976,RMVar_hsa_circ_277039,RMVar_hsa_circ_340389,RMVar_hsa_circ_173975,RMVar_hsa_circ_378559,RMVar_hsa_circ_173979,RMVar_hsa_circ_284646,RMVar_hsa_circ_328057,RMVar_hsa_circ_173978 48235 RMVar_ID_48235 Human_SNP_ID_583462314 A-to-I Human chr15 - 75541156 75541156 75541156 TTGAGCCTAGGACTTCAAGGTTACACTGAGCTATGATCATGCCACTGCACTCAAGCCTGGGCAAG TTGAGCCTAGGACTTCAAGGTTACACTGAGCTGTGATCATGCCACTGCACTCAAGCCTGGGCAAG T C PTPN9,AC105036.3 Ensembl:ENSG00000169410,Ensembl:ENSG00000260269 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223739130 Functional Loss SNV dbSNP153 33..33 33 - - - 48236 RMVar_ID_48236 Human_SNP_ID_583462340 A-to-I Human chr15 - 75541260 75541260 75541260 TCGGCTGGTGAGACCCTATCTCTACAAAAATTAAAAAAGTAGCCAGATGTGGTGGCACACACCTG TCGGCTGGTGAGACCCTATCTCTACAAAAATTTAAAAAGTAGCCAGATGTGGTGGCACACACCTG T A PTPN9,AC105036.3 Ensembl:ENSG00000169410,Ensembl:ENSG00000260269 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1407293122 Functional Loss SNV dbSNP153 33..33 33 - - - 48237 RMVar_ID_48237 Human_SNP_ID_583464202 A-to-I Human chr15 - 75549284 75549284 75549284 AGGCAGGAGGATCACTTGCACCTGGGAGGTCAAGACTGCAGTGAGCCATGTCCTCACCACTGTAA AGGCAGGAGGATCACTTGCACCTGGGAGGTCAGGACTGCAGTGAGCCATGTCCTCACCACTGTAA T C PTPN9,AC105036.3 Ensembl:ENSG00000169410,Ensembl:ENSG00000260269 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs944502145 Functional Loss SNV dbSNP153 33..33 33 - - - 48238 RMVar_ID_48238 Human_SNP_ID_583464325 A-to-I Human chr15 - 75549887 75549887 75549887 TCACTGCAGCCTTAACTTCCCATGCTTAAGCAATCCTCCCACCTCAGCCTCCCGAGTAGCTGGGA TCACTGCAGCCTTAACTTCCCATGCTTAAGCAGTCCTCCCACCTCAGCCTCCCGAGTAGCTGGGA T C PTPN9,AC105036.3 Ensembl:ENSG00000169410,Ensembl:ENSG00000260269 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1418556303 Functional Loss SNV dbSNP153 33..33 33 - - - 48239 RMVar_ID_48239 Human_SNP_ID_583464326 A-to-I Human chr15 - 75549887 75549887 75549887 TCACTGCAGCCTTAACTTCCCATGCTTAAGCAATCCTCCCACCTCAGCCTCCCGAGTAGCTGGGA TCACTGCAGCCTTAACTTCCCATGCTTAAGCACTCCTCCCACCTCAGCCTCCCGAGTAGCTGGGA T G PTPN9,AC105036.3 Ensembl:ENSG00000169410,Ensembl:ENSG00000260269 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1418556303 Functional Loss SNV dbSNP153 33..33 33 - - - 48240 RMVar_ID_48240 Human_SNP_ID_583468256 A-to-I Human chr15 - 75564727 75564727 75564727 TTCTCAAATTCCTTGCCTCAAGGGATCCTCCTACCTTGCCCTCCCAAAGTGTTAGAATACAGGCA TTCTCAAATTCCTTGCCTCAAGGGATCCTCCTGCCTTGCCCTCCCAAAGTGTTAGAATACAGGCA T C PTPN9,AC105036.3 Ensembl:ENSG00000169410,Ensembl:ENSG00000260269 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1040640511 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3490577,Human_RBP_ID_5247115 48241 RMVar_ID_48241 Human_SNP_ID_583469561 A-to-I Human chr15 - 75569907 75569906 75569907 CTGAGGCAGGAGAATTGCTTGAACCGGGAGGCAGGGGTTGCTGTGAGCTGAGATCGCGCCACTGC CTGAGGCAGGAGAATTGCTTGAACCGGGAGGC_GGGGTTGCTGTGAGCTGAGATCGCGCCACTGC CT C PTPN9,AC105036.3 Ensembl:ENSG00000169410,Ensembl:ENSG00000260269 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167761401 Functional Loss DEL dbSNP153 33..33 33 - - - 48242 RMVar_ID_48242 Human_SNP_ID_583474946 A-to-I Human chr15 - 75591560 75591560 75591560 CCTGGCCAACAGAGCGAGACCTTGTCTCTACAAAAAATTTAAAAATTAGTTGGGCATGGTGATAG CCTGGCCAACAGAGCGAGACCTTGTCTCTACACAAAATTTAAAAATTAGTTGGGCATGGTGATAG T G AC105036.3 Ensembl:ENSG00000260269 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1360394802 Functional Loss SNV dbSNP153 33..33 33 - - - 48243 RMVar_ID_48243 Human_SNP_ID_583475304 A-to-I Human chr15 - 75593215 75593215 75593215 CATTCAAAAATATCAAGATGTGGGCTGGGCGCAGTGGCTCATGCCTGTAATCCCAGTGCTTTGGG CATTCAAAAATATCAAGATGTGGGCTGGGCGCGGTGGCTCATGCCTGTAATCCCAGTGCTTTGGG T C AC105036.3 Ensembl:ENSG00000260269 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1186292419 Functional Loss SNV dbSNP153 33..33 33 - - - 48244 RMVar_ID_48244 Human_SNP_ID_583477047 A-to-I Human chr15 - 75600512 75600512 75600512 CCAGCACTTGGGAAGGCCGAGGCCGGTGGATCACTTGAGGTCAGGAGTTCAAGACCAGCCTGGCC CCAGCACTTGGGAAGGCCGAGGCCGGTGGATCGCTTGAGGTCAGGAGTTCAAGACCAGCCTGGCC T C AC105036.3,SNUPN Ensembl:ENSG00000260269,Ensembl:ENSG00000169371 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1198460564 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82458,RMVar_hsa_circ_173982,RMVar_hsa_circ_173984,RMVar_hsa_circ_173983 48245 RMVar_ID_48245 Human_SNP_ID_583477059 A-to-I Human chr15 - 75600566 75600566 75600566 TTTTAGCACTGAAAGTCTCACAGCGGCTGGGCATGGTGGCTCACGCCTATAATCCCAGCACTTGG TTTTAGCACTGAAAGTCTCACAGCGGCTGGGCGTGGTGGCTCACGCCTATAATCCCAGCACTTGG T C AC105036.3,SNUPN Ensembl:ENSG00000260269,Ensembl:ENSG00000169371 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1379338060 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82458,RMVar_hsa_circ_173982,RMVar_hsa_circ_173984,RMVar_hsa_circ_173983 48246 RMVar_ID_48246 Human_SNP_ID_583477060 A-to-I Human chr15 - 75600566 75600566 75600566 TTTTAGCACTGAAAGTCTCACAGCGGCTGGGCATGGTGGCTCACGCCTATAATCCCAGCACTTGG TTTTAGCACTGAAAGTCTCACAGCGGCTGGGCCTGGTGGCTCACGCCTATAATCCCAGCACTTGG T G AC105036.3,SNUPN Ensembl:ENSG00000260269,Ensembl:ENSG00000169371 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1379338060 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82458,RMVar_hsa_circ_173982,RMVar_hsa_circ_173984,RMVar_hsa_circ_173983 48247 RMVar_ID_48247 Human_SNP_ID_583477641 A-to-I Human chr15 - 75602779 75602779 75602779 AACACAGCAGAACCCCATCTCTACAAAAAAATACAAAAACAGATTAGGCATGGTGGCGTGCACCT AACACAGCAGAACCCCATCTCTACAAAAAAATGCAAAAACAGATTAGGCATGGTGGCGTGCACCT T C SNUPN Ensembl:ENSG00000169371 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1212881972 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82458,RMVar_hsa_circ_173982,RMVar_hsa_circ_173983,RMVar_hsa_circ_323168 48248 RMVar_ID_48248 Human_SNP_ID_583482268 A-to-I Human chr15 - 75621470 75621470 75621470 ATTGCTTGAGCCCAAGAGTTCAAGACTAGCCTAGGCAACATAGGGAGATCCCGTCTGTACCAATA ATTGCTTGAGCCCAAGAGTTCAAGACTAGCCTGGGCAACATAGGGAGATCCCGTCTGTACCAATA T C SNUPN Ensembl:ENSG00000169371 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs993620680 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_359037 48249 RMVar_ID_48249 Human_SNP_ID_583482793 A-to-I Human chr15 - 75623585 75623585 75623585 CAAAAATTAGCCGAGCATGGTGGTGCATGTCTATAATCCCAGCTACTCAGGAGGCTGAGGCAGGA CAAAAATTAGCCGAGCATGGTGGTGCATGTCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGA T C SNUPN Ensembl:ENSG00000169371 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs977735113 Functional Loss SNV dbSNP153 33..33 33 - - - 48250 RMVar_ID_48250 Human_SNP_ID_583488515 A-to-I Human chr15 - 75644737 75644737 75644737 GGGCTTTTCACTATGTTGCCCAGGCTGATCTCAAACTCCTGGGCTCAAGCAATCCTTCTGCCTCG GGGCTTTTCACTATGTTGCCCAGGCTGATCTCTAACTCCTGGGCTCAAGCAATCCTTCTGCCTCG T A IMP3 Ensembl:ENSG00000177971 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1343778507 Functional Loss SNV dbSNP153 33..33 33 - - - 48251 RMVar_ID_48251 Human_SNP_ID_583554265 A-to-I Human chr15 + 75907820 75907820 75907820 CAAAAGTTGGCTGGGCATGTTAGTGCAAACCTATAATCGCAGCTACTTGGGTAGCTGAGGTACCA CAAAAGTTGGCTGGGCATGTTAGTGCAAACCTGTAATCGCAGCTACTTGGGTAGCTGAGGTACCA A G FBXO22 Ensembl:ENSG00000167196 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1043152413 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_377209 48252 RMVar_ID_48252 Human_SNP_ID_583563738 A-to-I Human chr15 - 75949359 75949359 75949359 TCACCCAGGCTGGAGTGCAGTGGCATGACCTCAGCATACTGCAACCTCTGCCTCCTAGGTTCAAT TCACCCAGGCTGGAGTGCAGTGGCATGACCTCGGCATACTGCAACCTCTGCCTCCTAGGTTCAAT T C NRG4 Ensembl:ENSG00000169752 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs540492647 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123920,RMVar_hsa_circ_369030,RMVar_hsa_circ_174021,RMVar_hsa_circ_354277,RMVar_hsa_circ_174022 48253 RMVar_ID_48253 Human_SNP_ID_583574359 A-to-I Human chr15 - 75999771 75999771 75999771 TCGGCCTCCCAAAGTGCTGGGATTATAGGTATAAGCCACTGTGCCAAGTCTCTATTTGGATTATG TCGGCCTCCCAAAGTGCTGGGATTATAGGTATGAGCCACTGTGCCAAGTCTCTATTTGGATTATG T C NRG4 Ensembl:ENSG00000169752 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1047048236 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79066,RMVar_hsa_circ_123920,RMVar_hsa_circ_174021,RMVar_hsa_circ_174022,RMVar_hsa_circ_362469,RMVar_hsa_circ_67082,RMVar_hsa_circ_174023 48254 RMVar_ID_48254 Human_SNP_ID_583616390 A-to-I Human chr15 + 76183390 76183390 76183390 CACCCACCTCGGCCTCCCAAAGTGCAGGGATTACAGGTGGGAGCCACCAAGCCCGGCCGATCCTT CACCCACCTCGGCCTCCCAAAGTGCAGGGATTTCAGGTGGGAGCCACCAAGCCCGGCCGATCCTT A T TMEM266 Ensembl:ENSG00000169758 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1477316017 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26702,RMVar_hsa_circ_376813 48255 RMVar_ID_48255 Human_SNP_ID_583628211 A-to-I Human chr15 - 76230061 76230061 76230061 TCACTGCTAGCTCCGCCTCCCGCGTTCACGCCATTCTCCTGCCTCAGCCTCCCAAAGTGCTGGGA TCACTGCTAGCTCCGCCTCCCGCGTTCACGCCGTTCTCCTGCCTCAGCCTCCCAAAGTGCTGGGA T C ETFA,AC027243.1 Ensembl:ENSG00000140374,Ensembl:ENSG00000196274 Protein coding,Other intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1019700744 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118874,RMVar_hsa_circ_122278,RMVar_hsa_circ_174026,RMVar_hsa_circ_174027,RMVar_hsa_circ_174029,RMVar_hsa_circ_63661,RMVar_hsa_circ_288511,RMVar_hsa_circ_302991,RMVar_hsa_circ_363997,RMVar_hsa_circ_70593,RMVar_hsa_circ_11079,RMVar_hsa_circ_174028 48256 RMVar_ID_48256 Human_SNP_ID_583642767 A-to-I Human chr15 - 76290420 76290420 76290420 GAATTGCTTGAGCCTGGAAGGTTGAGGCTGCAATGAGCTGAGATTACACTGCTGCACTCCAGCCT GAATTGCTTGAGCCTGGAAGGTTGAGGCTGCAGTGAGCTGAGATTACACTGCTGCACTCCAGCCT T C ETFA Ensembl:ENSG00000140374 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs140689658 Functional Loss SNV dbSNP153 33..33 33 - - - 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_282226,RMVar_hsa_circ_174050,RMVar_hsa_circ_60126,RMVar_hsa_circ_365732,RMVar_hsa_circ_310688,RMVar_hsa_circ_174052,RMVar_hsa_circ_174051 48257 RMVar_ID_48257 Human_SNP_ID_583642894 A-to-I Human chr15 - 76291033 76291033 76291033 TTTCAAATTTTTTGTATCGATGTAGTCTCCCTATGTTGTGCGGGCTTGTCTTAAACTCCTGGCCT TTTCAAATTTTTTGTATCGATGTAGTCTCCCTTTGTTGTGCGGGCTTGTCTTAAACTCCTGGCCT T A ETFA Ensembl:ENSG00000140374 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs939828150 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12598509 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_282226,RMVar_hsa_circ_174050,RMVar_hsa_circ_60126,RMVar_hsa_circ_365732,RMVar_hsa_circ_310688,RMVar_hsa_circ_174052,RMVar_hsa_circ_174051 48258 RMVar_ID_48258 Human_SNP_ID_583642895 A-to-I Human chr15 - 76291033 76291033 76291033 TTTCAAATTTTTTGTATCGATGTAGTCTCCCTATGTTGTGCGGGCTTGTCTTAAACTCCTGGCCT TTTCAAATTTTTTGTATCGATGTAGTCTCCCTGTGTTGTGCGGGCTTGTCTTAAACTCCTGGCCT T C ETFA Ensembl:ENSG00000140374 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs939828150 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12598509 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_282226,RMVar_hsa_circ_174050,RMVar_hsa_circ_60126,RMVar_hsa_circ_365732,RMVar_hsa_circ_310688,RMVar_hsa_circ_174052,RMVar_hsa_circ_174051 48259 RMVar_ID_48259 Human_SNP_ID_583720151 A-to-I Human chr15 - 76620014 76620014 76620014 TGGAAGGCAGTGGCATGATCTAGGCTCACTGCAACCTCTGCCTCCCAGGTTCGGGCAATTCTTGT TGGAAGGCAGTGGCATGATCTAGGCTCACTGCCACCTCTGCCTCCCAGGTTCGGGCAATTCTTGT T G SCAPER Ensembl:ENSG00000140386 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879728267 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2095,RMVar_hsa_circ_341180,RMVar_hsa_circ_332580,RMVar_hsa_circ_60748,RMVar_hsa_circ_288098,RMVar_hsa_circ_308983,RMVar_hsa_circ_360683,RMVar_hsa_circ_354998,RMVar_hsa_circ_316630,RMVar_hsa_circ_349934,RMVar_hsa_circ_378067,RMVar_hsa_circ_269879,RMVar_hsa_circ_5017,RMVar_hsa_circ_60507,RMVar_hsa_circ_174066 48260 RMVar_ID_48260 Human_SNP_ID_583799652 A-to-I Human chr15 + 76943245 76943245 76943245 GTTTTGTTTGTTTTTTGAGTCAGGGTCTTGCTATGGTGTGAAGGCTGGCCTTGAACTTCTGGGCT GTTTTGTTTGTTTTTTGAGTCAGGGTCTTGCTCTGGTGTGAAGGCTGGCCTTGAACTTCTGGGCT A C RCN2 Ensembl:ENSG00000117906 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879803304 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12599870 48261 RMVar_ID_48261 Human_SNP_ID_583799653 A-to-I Human chr15 + 76943245 76943245 76943245 GTTTTGTTTGTTTTTTGAGTCAGGGTCTTGCTATGGTGTGAAGGCTGGCCTTGAACTTCTGGGCT GTTTTGTTTGTTTTTTGAGTCAGGGTCTTGCTGTGGTGTGAAGGCTGGCCTTGAACTTCTGGGCT A G RCN2 Ensembl:ENSG00000117906 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879803304 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12599870 48262 RMVar_ID_48262 Human_SNP_ID_583832121 A-to-I Human chr15 - 77066489 77066489 77066489 TGGCTGACTGCAGCCTCTGTCTCCCGGGTTCAAGCGATCTTCCTGCCTCAGCCTCCCGAGTAGCT TGGCTGACTGCAGCCTCTGTCTCCCGGGTTCAGGCGATCTTCCTGCCTCAGCCTCCCGAGTAGCT T C TSPAN3 Ensembl:ENSG00000140391 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs972299874 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6466899,Human_RBP_ID_12600455 48263 RMVar_ID_48263 Human_SNP_ID_583865222 A-to-I Human chr15 - 77200113 77200113 77200113 GAGGAGGAGGAAGAAGAAGGGTTGGTTTTGCTATCTCAAGGGTGACAGAGGCAGAAGAGACTGAA GAGGAGGAGGAAGAAGAAGGGTTGGTTTTGCTCTCTCAAGGGTGACAGAGGCAGAAGAGACTGAA T G PEAK1 Ensembl:ENSG00000173517 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs755616176 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74172,RMVar_hsa_circ_60590,RMVar_hsa_circ_348446,RMVar_hsa_circ_16365,RMVar_hsa_circ_293762,RMVar_hsa_circ_347199 48264 RMVar_ID_48264 Human_SNP_ID_583903675 A-to-I Human chr15 - 77357046 77357046 77357046 TCAAGGCTGATCTTGAACTCCTGGGCTCAGGTAATCCTTCCACCTCAGCCTCCCAAAGTGCTGGG TCAAGGCTGATCTTGAACTCCTGGGCTCAGGTGATCCTTCCACCTCAGCCTCCCAAAGTGCTGGG T C PEAK1 Ensembl:ENSG00000173517 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1461297690 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60590,RMVar_hsa_circ_113592,RMVar_hsa_circ_290973,RMVar_hsa_circ_174113,RMVar_hsa_circ_314092,RMVar_hsa_circ_174114,RMVar_hsa_circ_174118,RMVar_hsa_circ_124435,RMVar_hsa_circ_350805 48265 RMVar_ID_48265 Human_SNP_ID_583908328 A-to-I Human chr15 - 77377167 77377167 77377167 ATGTTGCCTAGGTTGGTCTCAAACAGGGCTCAAGTGATCCTCTCACCTTGGTCTCCCAAAGTGTT ATGTTGCCTAGGTTGGTCTCAAACAGGGCTCAGGTGATCCTCTCACCTTGGTCTCCCAAAGTGTT T C PEAK1 Ensembl:ENSG00000173517 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1371481117 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113592,RMVar_hsa_circ_174113,RMVar_hsa_circ_174119 48266 RMVar_ID_48266 Human_SNP_ID_583929147 A-to-I Human chr15 + 77465629 77465629 77465629 GTTGACCAGGCTGGTCTCGAAATTCTGACCTCAAGTGATCCGCCTGCCTTGGCCCTCCAAAGTGC GTTGACCAGGCTGGTCTCGAAATTCTGACCTCGAGTGATCCGCCTGCCTTGGCCCTCCAAAGTGC A G HMG20A Ensembl:ENSG00000140382 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs573186225 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7085,RMVar_hsa_circ_40085,RMVar_hsa_circ_174120,RMVar_hsa_circ_324240,RMVar_hsa_circ_349703,RMVar_hsa_circ_174121,RMVar_hsa_circ_68266,RMVar_hsa_circ_338921,RMVar_hsa_circ_174122,RMVar_hsa_circ_174123 48267 RMVar_ID_48267 Human_SNP_ID_583933417 A-to-I Human chr15 - 77484909 77484909 77484909 AAAACTGAACACAAATGAGAAACAGAAATATGAGGAGGAAGGAAGACAGGACACAAAGCATCTGG AAAACTGAACACAAATGAGAAACAGAAATATGCGGAGGAAGGAAGACAGGACACAAAGCATCTGG T G AC090984.1 Ensembl:ENSG00000279033 Other exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1273109169 Functional Loss SNV dbSNP153 33..33 33 - - - 48268 RMVar_ID_48268 Human_SNP_ID_583965552 A-to-I Human chr15 - 77614900 77614900 77614900 GGTGGAGCCCTATGCCTTCCGCGGCCTCAACTACCTGCGCGTGCTCAATGTCTCTGGCAACCAGC GGTGGAGCCCTATGCCTTCCGCGGCCTCAACTGCCTGCGCGTGCTCAATGTCTCTGGCAACCAGC T C LINGO1 Ensembl:ENSG00000169783 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs765997120 Functional Loss SNV dbSNP153 33..33 33 - - - 48269 RMVar_ID_48269 Human_SNP_ID_584071773 A-to-I Human chr15 - 78022772 78022772 78022772 GACTGAGGTGGGCACATTGCTTGAGCCCAGGAATTTGAGACCAGTGTAGGCAACATAGTGAAACC GACTGAGGTGGGCACATTGCTTGAGCCCAGGAGTTTGAGACCAGTGTAGGCAACATAGTGAAACC T C TBC1D2B Ensembl:ENSG00000167202 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1013410834 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76029,RMVar_hsa_circ_372447,RMVar_hsa_circ_35968,RMVar_hsa_circ_12473,RMVar_hsa_circ_331548,RMVar_hsa_circ_174133,RMVar_hsa_circ_174134,RMVar_hsa_circ_316083,RMVar_hsa_circ_67528,RMVar_hsa_circ_103890,RMVar_hsa_circ_174137,RMVar_hsa_circ_174136,RMVar_hsa_circ_349773,RMVar_hsa_circ_174140,RMVar_hsa_circ_174139,RMVar_hsa_circ_174141 48270 RMVar_ID_48270 Human_SNP_ID_584083030 A-to-I Human chr15 - 78069944 78069944 78069944 GTGCTGCTGTGAAAAAATACCGTAGACAGGGTAGCTTATAAACAACAGAAATTTATTTCTCATAG GTGCTGCTGTGAAAAAATACCGTAGACAGGGTGGCTTATAAACAACAGAAATTTATTTCTCATAG T C TBC1D2B Ensembl:ENSG00000167202 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs558317393 Functional Loss SNV dbSNP153 33..33 33 - - - 48271 RMVar_ID_48271 Human_SNP_ID_584092840 A-to-I Human chr15 - 78109364 78109364 78109364 TGTGTTTTCTTCAGGAGAATCCCTTCAAAGAAAGGATCGTGGCGGCGTTTTCCGAGGATGGTGAG TGTGTTTTCTTCAGGAGAATCCCTTCAAAGAAGGGATCGTGGCGGCGTTTTCCGAGGATGGTGAG T C CIB2 Ensembl:ENSG00000136425 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1338080083 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1631318,Human_Splice_Rec_1631326,Human_Splice_Rec_1631332,Human_Splice_Rec_1631346,Human_Splice_Rec_1631354,Human_Splice_Rec_1631364,Human_Splice_Rec_1631370,Human_Splice_Rec_1631386 RMVar_hsa_circ_88062,RMVar_hsa_circ_174146,RMVar_hsa_circ_174150,RMVar_hsa_circ_174147,RMVar_hsa_circ_345745,RMVar_hsa_circ_124610,RMVar_hsa_circ_337572,RMVar_hsa_circ_174149 48272 RMVar_ID_48272 Human_SNP_ID_584102686 A-to-I Human chr15 + 78151298 78151298 78151298 CCTCTGTTGAGTTTCCATTTCAGGTTGTGGCCAGGCATGGTGGCTCATGCCTGTAATTCTAGCAC CCTCTGTTGAGTTTCCATTTCAGGTTGTGGCCGGGCATGGTGGCTCATGCCTGTAATTCTAGCAC A G IDH3A Ensembl:ENSG00000166411 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1195140699 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12602897 Human_Splice_Rec_1631452 48273 RMVar_ID_48273 Human_SNP_ID_584102711 A-to-I Human chr15 + 78151405 78151405 78151405 CAAGACCAGCCTGGCCAACATGGCGAAACCCCATCTCTACTAAAAATACAAAAATTTGCTGGGCG CAAGACCAGCCTGGCCAACATGGCGAAACCCCGTCTCTACTAAAAATACAAAAATTTGCTGGGCG A G IDH3A Ensembl:ENSG00000166411 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs940320436 Functional Loss SNV dbSNP153 33..33 33 - - - 48274 RMVar_ID_48274 Human_SNP_ID_584102839 A-to-I Human chr15 + 78151874 78151874 78151874 CTGCCATCTCAGCCTTCCATGAAGCTGGGACTACTGGTGTGTGCCACCATACCTGGCTAACATTT CTGCCATCTCAGCCTTCCATGAAGCTGGGACTGCTGGTGTGTGCCACCATACCTGGCTAACATTT A G IDH3A Ensembl:ENSG00000166411 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1461184975 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_124917,Human_RBP_ID_12602917 48275 RMVar_ID_48275 Human_SNP_ID_584103335 A-to-I Human chr15 + 78153975 78153975 78153975 GTGGTTGCAGTGAGCCGAGATTGCACCATTGCACTCCAGCCTGGGCAACAAGAGTGAAACTCTGT GTGGTTGCAGTGAGCCGAGATTGCACCATTGCTCTCCAGCCTGGGCAACAAGAGTGAAACTCTGT A T IDH3A Ensembl:ENSG00000166411 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs537223829 Functional Loss SNV dbSNP153 33..33 33 - - - 48276 RMVar_ID_48276 Human_SNP_ID_584178990 A-to-I Human chr15 + 78455483 78455483 78455483 TGGACATAGTGTCTCCTGCCTTTAATCCCAGCACTTTGGAAGGCCAAGGCTGGAGGATTGCTCGA TGGACATAGTGTCTCCTGCCTTTAATCCCAGCCCTTTGGAAGGCCAAGGCTGGAGGATTGCTCGA A C IREB2 Ensembl:ENSG00000136381 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432176110 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15491,RMVar_hsa_circ_76692,RMVar_hsa_circ_58791,RMVar_hsa_circ_174166 48277 RMVar_ID_48277 Human_SNP_ID_584182081 A-to-I Human chr15 + 78467896 78467896 78467896 TTTTGTTTTGTTTTGAGACAGAGTCTCACTCTATTGCCTGGGCTGAAGTGCAGTGTCATAAGCAT TTTTGTTTTGTTTTGAGACAGAGTCTCACTCTGTTGCCTGGGCTGAAGTGCAGTGTCATAAGCAT A G IREB2 Ensembl:ENSG00000136381 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1277567896 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12604556 RMVar_hsa_circ_8026,RMVar_hsa_circ_15491,RMVar_hsa_circ_58791,RMVar_hsa_circ_354964,RMVar_hsa_circ_376160,RMVar_hsa_circ_372734,RMVar_hsa_circ_296978,RMVar_hsa_circ_30449,RMVar_hsa_circ_37463,RMVar_hsa_circ_22664,RMVar_hsa_circ_28501,RMVar_hsa_circ_174169,RMVar_hsa_circ_174170,RMVar_hsa_circ_301677,RMVar_hsa_circ_361559,RMVar_hsa_circ_174168,RMVar_hsa_circ_306768,RMVar_hsa_circ_174173,RMVar_hsa_circ_174174,RMVar_hsa_circ_53625 48278 RMVar_ID_48278 Human_SNP_ID_584185800 A-to-I Human chr15 + 78481346 78481346 78481346 TGCCTCAGCCTCCTGAGTAGCTAGGATTACAGACATGCGCCACCATGCCCGGCTTTTTTTTTTGA TGCCTCAGCCTCCTGAGTAGCTAGGATTACAGGCATGCGCCACCATGCCCGGCTTTTTTTTTTGA A G IREB2 Ensembl:ENSG00000136381 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs8041085 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25917,RMVar_hsa_circ_15491,RMVar_hsa_circ_376160,RMVar_hsa_circ_372734,RMVar_hsa_circ_296978,RMVar_hsa_circ_37463,RMVar_hsa_circ_49009,RMVar_hsa_circ_28501,RMVar_hsa_circ_174169,RMVar_hsa_circ_361559,RMVar_hsa_circ_174168,RMVar_hsa_circ_174174,RMVar_hsa_circ_339588,RMVar_hsa_circ_53625,RMVar_hsa_circ_329470,RMVar_hsa_circ_296501,RMVar_hsa_circ_346994,RMVar_hsa_circ_304423,RMVar_hsa_circ_345142,RMVar_hsa_circ_174179,RMVar_hsa_circ_42985,RMVar_hsa_circ_285778,RMVar_hsa_circ_336611,RMVar_hsa_circ_375490,RMVar_hsa_circ_376678,RMVar_hsa_circ_301833,RMVar_hsa_circ_174181,RMVar_hsa_circ_174180,RMVar_hsa_circ_55473,RMVar_hsa_circ_285363,RMVar_hsa_circ_174178,RMVar_hsa_circ_297025,RMVar_hsa_circ_279842,RMVar_hsa_circ_174184,RMVar_hsa_circ_10724,RMVar_hsa_circ_174185 48279 RMVar_ID_48279 Human_SNP_ID_584185801 A-to-I Human chr15 + 78481346 78481346 78481346 TGCCTCAGCCTCCTGAGTAGCTAGGATTACAGACATGCGCCACCATGCCCGGCTTTTTTTTTTGA TGCCTCAGCCTCCTGAGTAGCTAGGATTACAGTCATGCGCCACCATGCCCGGCTTTTTTTTTTGA A T IREB2 Ensembl:ENSG00000136381 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs8041085 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25917,RMVar_hsa_circ_15491,RMVar_hsa_circ_376160,RMVar_hsa_circ_372734,RMVar_hsa_circ_296978,RMVar_hsa_circ_37463,RMVar_hsa_circ_49009,RMVar_hsa_circ_28501,RMVar_hsa_circ_174169,RMVar_hsa_circ_361559,RMVar_hsa_circ_174168,RMVar_hsa_circ_174174,RMVar_hsa_circ_339588,RMVar_hsa_circ_53625,RMVar_hsa_circ_329470,RMVar_hsa_circ_296501,RMVar_hsa_circ_346994,RMVar_hsa_circ_304423,RMVar_hsa_circ_345142,RMVar_hsa_circ_174179,RMVar_hsa_circ_42985,RMVar_hsa_circ_285778,RMVar_hsa_circ_336611,RMVar_hsa_circ_375490,RMVar_hsa_circ_376678,RMVar_hsa_circ_301833,RMVar_hsa_circ_174181,RMVar_hsa_circ_174180,RMVar_hsa_circ_55473,RMVar_hsa_circ_285363,RMVar_hsa_circ_174178,RMVar_hsa_circ_297025,RMVar_hsa_circ_279842,RMVar_hsa_circ_174184,RMVar_hsa_circ_10724,RMVar_hsa_circ_174185 48280 RMVar_ID_48280 Human_SNP_ID_584187200 A-to-I Human chr15 + 78486706 78486706 78486706 GATTTTTTGGTTTTGAGACAGTGTCTTGCTCTATTGCCCACACTGGAGTGCAGTGGTGCAATCAC GATTTTTTGGTTTTGAGACAGTGTCTTGCTCTGTTGCCCACACTGGAGTGCAGTGGTGCAATCAC A G IREB2 Ensembl:ENSG00000136381 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs113727781 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17563295 RMVar_hsa_circ_372734,RMVar_hsa_circ_296978,RMVar_hsa_circ_49009,RMVar_hsa_circ_28501,RMVar_hsa_circ_174168,RMVar_hsa_circ_339588,RMVar_hsa_circ_53625,RMVar_hsa_circ_329470,RMVar_hsa_circ_304423,RMVar_hsa_circ_345142,RMVar_hsa_circ_174179,RMVar_hsa_circ_42985,RMVar_hsa_circ_336611,RMVar_hsa_circ_376678,RMVar_hsa_circ_301833,RMVar_hsa_circ_55473,RMVar_hsa_circ_174178,RMVar_hsa_circ_297025,RMVar_hsa_circ_10724,RMVar_hsa_circ_174185,RMVar_hsa_circ_305205,RMVar_hsa_circ_9020,RMVar_hsa_circ_358877,RMVar_hsa_circ_43118 48281 RMVar_ID_48281 Human_SNP_ID_584187209 A-to-I Human chr15 + 78486749 78486748 78486749 TGGAGTGCAGTGGTGCAATCACAGCTCATTGCAGCCTCGACCTCCTAGGCTCAATCAGTCTTCCT TGGAGTGCAGTGGTGCAATCACAGCTCATTGC_GCCTCGACCTCCTAGGCTCAATCAGTCTTCCT CA C IREB2 Ensembl:ENSG00000136381 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs141285406 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_372734,RMVar_hsa_circ_296978,RMVar_hsa_circ_49009,RMVar_hsa_circ_28501,RMVar_hsa_circ_174168,RMVar_hsa_circ_339588,RMVar_hsa_circ_53625,RMVar_hsa_circ_329470,RMVar_hsa_circ_304423,RMVar_hsa_circ_345142,RMVar_hsa_circ_174179,RMVar_hsa_circ_42985,RMVar_hsa_circ_336611,RMVar_hsa_circ_376678,RMVar_hsa_circ_301833,RMVar_hsa_circ_55473,RMVar_hsa_circ_174178,RMVar_hsa_circ_297025,RMVar_hsa_circ_10724,RMVar_hsa_circ_174185,RMVar_hsa_circ_305205,RMVar_hsa_circ_9020,RMVar_hsa_circ_358877,RMVar_hsa_circ_43118 48282 RMVar_ID_48282 Human_SNP_ID_584187217 A-to-I Human chr15 + 78486773 78486773 78486773 CTCATTGCAGCCTCGACCTCCTAGGCTCAATCAGTCTTCCTACCTCAGCCTCCTGAGTGGCTGGG CTCATTGCAGCCTCGACCTCCTAGGCTCAATCGGTCTTCCTACCTCAGCCTCCTGAGTGGCTGGG A G IREB2 Ensembl:ENSG00000136381 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1420157041 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_372734,RMVar_hsa_circ_296978,RMVar_hsa_circ_49009,RMVar_hsa_circ_28501,RMVar_hsa_circ_174168,RMVar_hsa_circ_339588,RMVar_hsa_circ_53625,RMVar_hsa_circ_329470,RMVar_hsa_circ_304423,RMVar_hsa_circ_345142,RMVar_hsa_circ_174179,RMVar_hsa_circ_42985,RMVar_hsa_circ_336611,RMVar_hsa_circ_376678,RMVar_hsa_circ_301833,RMVar_hsa_circ_55473,RMVar_hsa_circ_174178,RMVar_hsa_circ_297025,RMVar_hsa_circ_10724,RMVar_hsa_circ_174185,RMVar_hsa_circ_305205,RMVar_hsa_circ_9020,RMVar_hsa_circ_358877,RMVar_hsa_circ_43118 48283 RMVar_ID_48283 Human_SNP_ID_584187798 A-to-I Human chr15 + 78488991 78488991 78488991 CCTGTAATCCCGACACTTTGGGAGGCTGAAGCAGGTTGATCACGTGAGGTCCGGAGCTCAAGACC CCTGTAATCCCGACACTTTGGGAGGCTGAAGCCGGTTGATCACGTGAGGTCCGGAGCTCAAGACC A C IREB2 Ensembl:ENSG00000136381 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs962995914 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_372734,RMVar_hsa_circ_296978,RMVar_hsa_circ_28501,RMVar_hsa_circ_174168,RMVar_hsa_circ_339588,RMVar_hsa_circ_53625,RMVar_hsa_circ_329470,RMVar_hsa_circ_174179,RMVar_hsa_circ_336611,RMVar_hsa_circ_376678,RMVar_hsa_circ_301833,RMVar_hsa_circ_55473,RMVar_hsa_circ_174178,RMVar_hsa_circ_297025,RMVar_hsa_circ_174185,RMVar_hsa_circ_305205,RMVar_hsa_circ_43118,RMVar_hsa_circ_174188,RMVar_hsa_circ_338597,RMVar_hsa_circ_372545,RMVar_hsa_circ_53006,RMVar_hsa_circ_174187,RMVar_hsa_circ_59265,RMVar_hsa_circ_174189,RMVar_hsa_circ_300639,RMVar_hsa_circ_72005,RMVar_hsa_circ_304856,RMVar_hsa_circ_174191,RMVar_hsa_circ_3471 48284 RMVar_ID_48284 Human_SNP_ID_584198097 A-to-I Human chr15 + 78528656 78528656 78528656 GAAACCCTGTTTCTAATAAAAATGCAAAAACTAGCTGGGCATGGTGACGCGTGCCTGTAATCTCA GAAACCCTGTTTCTAATAAAAATGCAAAAACTCGCTGGGCATGGTGACGCGTGCCTGTAATCTCA A C HYKK Ensembl:ENSG00000188266 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1011784124 Functional Loss SNV dbSNP153 33..33 33 - - - 48285 RMVar_ID_48285 Human_SNP_ID_584198110 A-to-I Human chr15 + 78528696 78528696 78528696 ATGGTGACGCGTGCCTGTAATCTCAGCTACTCAGAGGCTGAGGCAGAAGAATTGCTTGAACCCTA ATGGTGACGCGTGCCTGTAATCTCAGCTACTCCGAGGCTGAGGCAGAAGAATTGCTTGAACCCTA A C HYKK Ensembl:ENSG00000188266 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965438287 Functional Loss SNV dbSNP153 33..33 33 - - - 48286 RMVar_ID_48286 Human_SNP_ID_584198832 A-to-I Human chr15 + 78531720 78531719 78531721 CGCTGGCTAAATTTTGTATTTTTAATAGAAACAGGGTTTCACTACGTTGGATAGGCTGGTCTCGA CGCTGGCTAAATTTTGTATTTTTAATAGAAAC__GGTTTCACTACGTTGGATAGGCTGGTCTCGA CAG C HYKK Ensembl:ENSG00000188266 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1361866384 Functional Loss DEL dbSNP153 33..34 33 - - - 48287 RMVar_ID_48287 Human_SNP_ID_584289621 A-to-I Human chr15 + 78876118 78876118 78876118 CGCCACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGA CGCCACCACGCCCAGCTAATTTTTGTATTTTTGGTAGAGACGGGGTTTCACCATGTTGGCCAGGA A G MORF4L1 Ensembl:ENSG00000185787 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs899873122 Functional Loss SNV dbSNP153 33..33 33 - - - 48288 RMVar_ID_48288 Human_SNP_ID_584294144 A-to-I Human chr15 + 78890097 78890097 78890097 CAAAAATGAGCTGGGAGTGGTGGTGGGTGCCTATGGTCCCAGCTACTTGGAAGGCTGAGGCAGGA CAAAAATGAGCTGGGAGTGGTGGTGGGTGCCTGTGGTCCCAGCTACTTGGAAGGCTGAGGCAGGA A G MORF4L1 Ensembl:ENSG00000185787 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs932811154 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126988,RMVar_hsa_circ_174220,RMVar_hsa_circ_66592,RMVar_hsa_circ_108381,RMVar_hsa_circ_174223,RMVar_hsa_circ_346445,RMVar_hsa_circ_364877,RMVar_hsa_circ_279114,RMVar_hsa_circ_73070,RMVar_hsa_circ_174224,RMVar_hsa_circ_174225 48289 RMVar_ID_48289 Human_SNP_ID_584294145 A-to-I Human chr15 + 78890097 78890097 78890097 CAAAAATGAGCTGGGAGTGGTGGTGGGTGCCTATGGTCCCAGCTACTTGGAAGGCTGAGGCAGGA CAAAAATGAGCTGGGAGTGGTGGTGGGTGCCTTTGGTCCCAGCTACTTGGAAGGCTGAGGCAGGA A T MORF4L1 Ensembl:ENSG00000185787 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs932811154 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126988,RMVar_hsa_circ_174220,RMVar_hsa_circ_66592,RMVar_hsa_circ_108381,RMVar_hsa_circ_174223,RMVar_hsa_circ_346445,RMVar_hsa_circ_364877,RMVar_hsa_circ_279114,RMVar_hsa_circ_73070,RMVar_hsa_circ_174224,RMVar_hsa_circ_174225 48290 RMVar_ID_48290 Human_SNP_ID_584296741 A-to-I Human chr15 + 78898315 78898315 78898315 GAGGTCAGGAGTTCGACACCAGCCTGATGAACATGGAGAAACCCCATCTCTACTAAAAATACAAA GAGGTCAGGAGTTCGACACCAGCCTGATGAACGTGGAGAAACCCCATCTCTACTAAAAATACAAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs963619001 Functional Loss SNV dbSNP153 33..33 33 - - - 48291 RMVar_ID_48291 Human_SNP_ID_584296742 A-to-I Human chr15 + 78898315 78898315 78898315 GAGGTCAGGAGTTCGACACCAGCCTGATGAACATGGAGAAACCCCATCTCTACTAAAAATACAAA GAGGTCAGGAGTTCGACACCAGCCTGATGAACTTGGAGAAACCCCATCTCTACTAAAAATACAAA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs963619001 Functional Loss SNV dbSNP153 33..33 33 - - - 48292 RMVar_ID_48292 Human_SNP_ID_584296766 A-to-I Human chr15 + 78898378 78898378 78898378 AATATTAGCTGGGCGTTGTGGCGCACGCCTGTAATCCCAGCGACTCACGAGGCTGAGGCAGGAGA AATATTAGCTGGGCGTTGTGGCGCACGCCTGTGATCCCAGCGACTCACGAGGCTGAGGCAGGAGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1187557832 Functional Loss SNV dbSNP153 33..33 33 - - - 48293 RMVar_ID_48293 Human_SNP_ID_584297090 A-to-I Human chr15 + 78899331 78899325 78899331 GCACCCGCCACCATGCCTGGCTAATTGTTTGTATTTTTAGTAGAGATGGGGTTTCGCCACGTTAG GCACCCGCCACCATGCCTGGCTAATTG______TTTTTAGTAGAGATGGGGTTTCGCCACGTTAG GTTTGTA G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1381749924 Functional Loss DEL dbSNP153 28..33 33 - - - 48294 RMVar_ID_48294 Human_SNP_ID_584297122 A-to-I Human chr15 + 78899435 78899435 78899435 CTTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGCACCCGGCTTCTACAAATAATT CTTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCACCCGGCTTCTACAAATAATT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs887582946 Functional Loss SNV dbSNP153 33..33 33 - - - 48295 RMVar_ID_48295 Human_SNP_ID_584297144 A-to-I Human chr15 + 78899500 78899500 78899500 TTATGAGTAGCCTGGCATGGTGGCGTGTGCCCATGGTCCCAGCTACCTGAGAGGCTGAGGCAGGA TTATGAGTAGCCTGGCATGGTGGCGTGTGCCCGTGGTCCCAGCTACCTGAGAGGCTGAGGCAGGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs953507039 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25171022 48296 RMVar_ID_48296 Human_SNP_ID_584310249 A-to-I Human chr15 - 78943503 78943503 78943503 GTCAGGGACCGGCTGCGGTGGCTCACACCTGTAATCTCAGCAATTTGGGAGACCGAGGCAGTCGG GTCAGGGACCGGCTGCGGTGGCTCACACCTGTGATCTCAGCAATTTGGGAGACCGAGGCAGTCGG T C CTSH Ensembl:ENSG00000103811 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1338471332 Functional Loss SNV dbSNP153 33..33 33 - - - 48297 RMVar_ID_48297 Human_SNP_ID_584310445 A-to-I Human chr15 - 78944306 78944306 78944306 GGTGGAGCCCCAGGACTCCTCTTGTTGGCCAGATTGGCTGCGACTGGTCCAGCTTCGTGCTGCCC GGTGGAGCCCCAGGACTCCTCTTGTTGGCCAGGTTGGCTGCGACTGGTCCAGCTTCGTGCTGCCC T C CTSH Ensembl:ENSG00000103811 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11072816 Functional Loss SNV dbSNP153 33..33 33 - - - 48298 RMVar_ID_48298 Human_SNP_ID_584548433 A-to-I Human chr15 - 79907673 79907673 79907673 GAGTTTCATTCTGTCGCCCAGGCTGGAGTGCAATGGCGCGATCTCGGCTCACTGCAACCTCTGTC GAGTTTCATTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCGATCTCGGCTCACTGCAACCTCTGTC T C ST20-MTHFS,ST20 Ensembl:ENSG00000259332,Ensembl:ENSG00000180953 Protein coding,Protein coding start codon,start codon GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1432690828 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1633642,Human_Splice_Rec_1633643,Human_Splice_Rec_1633648,Human_Splice_Rec_1633649,Human_Splice_Rec_1633657,Human_Splice_Rec_1633660,Human_Splice_Rec_1633661,Human_Splice_Rec_1633664,Human_Splice_Rec_1633665 RMVar_hsa_circ_97061,RMVar_hsa_circ_174247 48299 RMVar_ID_48299 Human_SNP_ID_584558896 A-to-I Human chr15 + 79945398 79945398 79945398 ACCAGATCCTGAAGGAAAATTACGGACAGAAGAAGGCCAAGAAGGTAGTCCAGGTGAAGGCACTG ACCAGATCCTGAAGGAAAATTACGGACAGAAGGAGGCCAAGAAGGTAGTCCAGGTGAAGGCACTG A G AC015871.1 Ensembl:ENSG00000259770 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1460602311 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1865009,Human_miRNA_ID_1867487,Human_miRNA_ID_1867782,Human_miRNA_ID_1871268 48300 RMVar_ID_48300 Human_SNP_ID_584589257 A-to-I Human chr15 + 80060870 80060870 80060870 TTGAACCCGGGAGGCGGAGGTTGCAGTGAACCAAGATCGCGCTACTGCACTCCAGCCTGGCGACA TTGAACCCGGGAGGCGGAGGTTGCAGTGAACCCAGATCGCGCTACTGCACTCCAGCCTGGCGACA A C ZFAND6 Ensembl:ENSG00000086666 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1377528540 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8424097,Human_RBP_ID_12610936,Human_RBP_ID_25188583 RMVar_hsa_circ_124644,RMVar_hsa_circ_102624,RMVar_hsa_circ_174249,RMVar_hsa_circ_174250 48301 RMVar_ID_48301 Human_SNP_ID_584595444 A-to-I Human chr15 + 80083770 80083770 80083770 AAAATCAGCTGGGCATGGTGGTGAGCATCTGTAATCCCAGCTACTCAGGAGGCTGAGGAGGTTGC AAAATCAGCTGGGCATGGTGGTGAGCATCTGTTATCCCAGCTACTCAGGAGGCTGAGGAGGTTGC A T ZFAND6 Ensembl:ENSG00000086666 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1430965499 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102391,RMVar_hsa_circ_124644,RMVar_hsa_circ_102624,RMVar_hsa_circ_174249,RMVar_hsa_circ_174252,RMVar_hsa_circ_348032,RMVar_hsa_circ_174250,RMVar_hsa_circ_294353,RMVar_hsa_circ_362363,RMVar_hsa_circ_174251,RMVar_hsa_circ_352024,RMVar_hsa_circ_174254,RMVar_hsa_circ_25124,RMVar_hsa_circ_174253 48302 RMVar_ID_48302 Human_SNP_ID_584596729 A-to-I Human chr15 + 80088973 80088973 80088973 TATCTCATCTTTATCCATAATAGACCCACCATAATCTTGCCCTTGCTTATCTCAGTATCCTCATC TATCTCATCTTTATCCATAATAGACCCACCATGATCTTGCCCTTGCTTATCTCAGTATCCTCATC A G ZFAND6 Ensembl:ENSG00000086666 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7183846 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5832,GWAS_ID_5833 RMVar_hsa_circ_102391,RMVar_hsa_circ_124644,RMVar_hsa_circ_102624,RMVar_hsa_circ_174249,RMVar_hsa_circ_348032,RMVar_hsa_circ_174250,RMVar_hsa_circ_294353,RMVar_hsa_circ_362363,RMVar_hsa_circ_174251,RMVar_hsa_circ_352024,RMVar_hsa_circ_174254,RMVar_hsa_circ_25124,RMVar_hsa_circ_174253 48303 RMVar_ID_48303 Human_SNP_ID_584596730 A-to-I Human chr15 + 80088973 80088973 80088973 TATCTCATCTTTATCCATAATAGACCCACCATAATCTTGCCCTTGCTTATCTCAGTATCCTCATC TATCTCATCTTTATCCATAATAGACCCACCATTATCTTGCCCTTGCTTATCTCAGTATCCTCATC A T ZFAND6 Ensembl:ENSG00000086666 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7183846 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5832,GWAS_ID_5833 RMVar_hsa_circ_102391,RMVar_hsa_circ_124644,RMVar_hsa_circ_102624,RMVar_hsa_circ_174249,RMVar_hsa_circ_348032,RMVar_hsa_circ_174250,RMVar_hsa_circ_294353,RMVar_hsa_circ_362363,RMVar_hsa_circ_174251,RMVar_hsa_circ_352024,RMVar_hsa_circ_174254,RMVar_hsa_circ_25124,RMVar_hsa_circ_174253 48304 RMVar_ID_48304 Human_SNP_ID_584596874 A-to-I Human chr15 + 80089338 80089338 80089338 AGGCTGGAGCAGTGGCACGATCTCCTCACTGTAGCCTCCACCTCCCTGGTTCAAGCAATTCTCCT AGGCTGGAGCAGTGGCACGATCTCCTCACTGTTGCCTCCACCTCCCTGGTTCAAGCAATTCTCCT A T ZFAND6 Ensembl:ENSG00000086666 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs769548396 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17563300 RMVar_hsa_circ_102391,RMVar_hsa_circ_124644,RMVar_hsa_circ_102624,RMVar_hsa_circ_174249,RMVar_hsa_circ_348032,RMVar_hsa_circ_174250,RMVar_hsa_circ_294353,RMVar_hsa_circ_362363,RMVar_hsa_circ_174251,RMVar_hsa_circ_352024,RMVar_hsa_circ_174254,RMVar_hsa_circ_25124,RMVar_hsa_circ_174253 48305 RMVar_ID_48305 Human_SNP_ID_584597538 A-to-I Human chr15 + 80091719 80091719 80091719 TGGAGTGCAGACGCACAATCATAGCTCACTGTAACCTCAAACTCCAGGACTGAAGCAGTCCTCTT TGGAGTGCAGACGCACAATCATAGCTCACTGTTACCTCAAACTCCAGGACTGAAGCAGTCCTCTT A T ZFAND6 Ensembl:ENSG00000086666 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs74638490 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12611831 RMVar_hsa_circ_102391,RMVar_hsa_circ_124644,RMVar_hsa_circ_102624,RMVar_hsa_circ_174249,RMVar_hsa_circ_348032,RMVar_hsa_circ_174250,RMVar_hsa_circ_294353,RMVar_hsa_circ_362363,RMVar_hsa_circ_174251,RMVar_hsa_circ_352024,RMVar_hsa_circ_174254,RMVar_hsa_circ_25124,RMVar_hsa_circ_174253 48306 RMVar_ID_48306 Human_SNP_ID_584597955 A-to-I Human chr15 + 80093167 80093167 80093167 GTGTGTGTTTTTAGTAGAGTCGGGGTTTCACCATGCTGACCAGGCTGGTTTCGAACTCCTGACCT GTGTGTGTTTTTAGTAGAGTCGGGGTTTCACCGTGCTGACCAGGCTGGTTTCGAACTCCTGACCT A G ZFAND6 Ensembl:ENSG00000086666 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1022418091 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102391,RMVar_hsa_circ_124644,RMVar_hsa_circ_102624,RMVar_hsa_circ_174249,RMVar_hsa_circ_348032,RMVar_hsa_circ_174250,RMVar_hsa_circ_294353,RMVar_hsa_circ_362363,RMVar_hsa_circ_174251,RMVar_hsa_circ_352024,RMVar_hsa_circ_174254,RMVar_hsa_circ_25124,RMVar_hsa_circ_174253 48307 RMVar_ID_48307 Human_SNP_ID_584597978 A-to-I Human chr15 + 80093230 80093230 80093230 CTCGTGATCCGCCTGCCTCGGCCTCCCAAAGTACTGGGATTACTAGCGTGAGCCACCATGCCCAG CTCGTGATCCGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACTAGCGTGAGCCACCATGCCCAG A G ZFAND6 Ensembl:ENSG00000086666 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1389863153 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102391,RMVar_hsa_circ_124644,RMVar_hsa_circ_102624,RMVar_hsa_circ_174249,RMVar_hsa_circ_348032,RMVar_hsa_circ_174250,RMVar_hsa_circ_294353,RMVar_hsa_circ_362363,RMVar_hsa_circ_174251,RMVar_hsa_circ_352024,RMVar_hsa_circ_174254,RMVar_hsa_circ_25124,RMVar_hsa_circ_174253 48308 RMVar_ID_48308 Human_SNP_ID_584597983 A-to-I Human chr15 + 80093239 80093239 80093239 CGCCTGCCTCGGCCTCCCAAAGTACTGGGATTACTAGCGTGAGCCACCATGCCCAGGCAGGACTT CGCCTGCCTCGGCCTCCCAAAGTACTGGGATTGCTAGCGTGAGCCACCATGCCCAGGCAGGACTT A G ZFAND6 Ensembl:ENSG00000086666 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs749266145 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25171696 RMVar_hsa_circ_102391,RMVar_hsa_circ_124644,RMVar_hsa_circ_102624,RMVar_hsa_circ_174249,RMVar_hsa_circ_348032,RMVar_hsa_circ_174250,RMVar_hsa_circ_294353,RMVar_hsa_circ_362363,RMVar_hsa_circ_174251,RMVar_hsa_circ_352024,RMVar_hsa_circ_174254,RMVar_hsa_circ_25124,RMVar_hsa_circ_174253 48309 RMVar_ID_48309 Human_SNP_ID_584608376 A-to-I Human chr15 + 80133752 80133752 80133752 ATACTAGGACTTAAGGCAGGAGGAGATCGTCTAACTTTACTGTTTTGCGCAAATGCAGTTGGGTT ATACTAGGACTTAAGGCAGGAGGAGATCGTCTGACTTTACTGTTTTGCGCAAATGCAGTTGGGTT A G ZFAND6 Ensembl:ENSG00000086666 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs561547077 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12612719 48310 RMVar_ID_48310 Human_SNP_ID_584815062 A-to-I Human chr15 - 80975924 80975924 80975924 GTCTCACTCTGTTGCCCTCACTAGAGTGCAGTAGGATCACGGCTCACTGAAGTCTCTACCTACCG GTCTCACTCTGTTGCCCTCACTAGAGTGCAGTGGGATCACGGCTCACTGAAGTCTCTACCTACCG T C MESD Ensembl:ENSG00000117899 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 29129909,30559470 RNA-Seq:(High) rs1398335881 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89615,RMVar_hsa_circ_125787,RMVar_hsa_circ_174305,RMVar_hsa_circ_174306 48311 RMVar_ID_48311 Human_SNP_ID_584815068 A-to-I Human chr15 - 80975934 80975934 80975934 TTGAGACAGGGTCTCACTCTGTTGCCCTCACTAGAGTGCAGTAGGATCACGGCTCACTGAAGTCT TTGAGACAGGGTCTCACTCTGTTGCCCTCACTGGAGTGCAGTAGGATCACGGCTCACTGAAGTCT T C MESD Ensembl:ENSG00000117899 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs933861112 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89615,RMVar_hsa_circ_125787,RMVar_hsa_circ_174305,RMVar_hsa_circ_174306 48312 RMVar_ID_48312 Human_SNP_ID_584815823 A-to-I Human chr15 - 80978919 80978919 80978919 GCTTTTTCCCATTTACACTTGGTGAGTCATCAACTCTACTGAGATTCCACTCCCCTCCAAGCACC GCTTTTTCCCATTTACACTTGGTGAGTCATCAGCTCTACTGAGATTCCACTCCCCTCCAAGCACC T C MESD Ensembl:ENSG00000117899 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs373401966 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_465352,Human_RBP_ID_1509692,Human_RBP_ID_2456688,Human_RBP_ID_3484963,Human_RBP_ID_6471560,Human_RBP_ID_17251352,Human_RBP_ID_17366505,Human_RBP_ID_17484088,Human_RBP_ID_17867837,Human_RBP_ID_18436894,Human_RBP_ID_18669853,Human_RBP_ID_22388303,Human_RBP_ID_22496913,Human_RBP_ID_26809171,Human_RBP_ID_27235012,Human_RBP_ID_27437591 Human_miRNA_ID_2231239 RMVar_hsa_circ_89615,RMVar_hsa_circ_125787,RMVar_hsa_circ_174305,RMVar_hsa_circ_174307,RMVar_hsa_circ_174306,RMVar_hsa_circ_376626 48313 RMVar_ID_48313 Human_SNP_ID_584815824 A-to-I Human chr15 - 80978919 80978919 80978919 GCTTTTTCCCATTTACACTTGGTGAGTCATCAACTCTACTGAGATTCCACTCCCCTCCAAGCACC GCTTTTTCCCATTTACACTTGGTGAGTCATCACCTCTACTGAGATTCCACTCCCCTCCAAGCACC T G MESD Ensembl:ENSG00000117899 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs373401966 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_465352,Human_RBP_ID_1509692,Human_RBP_ID_2456688,Human_RBP_ID_3484963,Human_RBP_ID_6471560,Human_RBP_ID_17251352,Human_RBP_ID_17366505,Human_RBP_ID_17484088,Human_RBP_ID_17867837,Human_RBP_ID_18436894,Human_RBP_ID_18669853,Human_RBP_ID_22388303,Human_RBP_ID_22496913,Human_RBP_ID_26809171,Human_RBP_ID_27235012,Human_RBP_ID_27437591 Human_miRNA_ID_2231239 RMVar_hsa_circ_89615,RMVar_hsa_circ_125787,RMVar_hsa_circ_174305,RMVar_hsa_circ_174307,RMVar_hsa_circ_174306,RMVar_hsa_circ_376626 48314 RMVar_ID_48314 Human_SNP_ID_584816403 A-to-I Human chr15 - 80980847 80980847 80980847 TGCACTCCAGCCTGGCGGCAGAGCAAGACTCCATCTCGGGGAAGAAAAAAAAAAAAAAAGGGCAT TGCACTCCAGCCTGGCGGCAGAGCAAGACTCCGTCTCGGGGAAGAAAAAAAAAAAAAAAGGGCAT T C MESD Ensembl:ENSG00000117899 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1171329251 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89615,RMVar_hsa_circ_125787,RMVar_hsa_circ_174305,RMVar_hsa_circ_174307,RMVar_hsa_circ_174306,RMVar_hsa_circ_376626,RMVar_hsa_circ_174308,RMVar_hsa_circ_270712 48315 RMVar_ID_48315 Human_SNP_ID_584818340 A-to-I Human chr15 - 80987941 80987941 80987941 TAAATTATTTTTTATAGAGACAGGGTCTCCTTATGTTGGCTGGGCTGGTTTTGAACTCTTGGCCT TAAATTATTTTTTATAGAGACAGGGTCTCCTTCTGTTGGCTGGGCTGGTTTTGAACTCTTGGCCT T G MESD Ensembl:ENSG00000117899 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs989098739 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6471607,Human_RBP_ID_8424271,Human_RBP_ID_12613318 RMVar_hsa_circ_89615,RMVar_hsa_circ_174306 48316 RMVar_ID_48316 Human_SNP_ID_584827398 A-to-I Human chr15 + 81021965 81021964 81021965 CACGATCATGGCTCACTGTAGTCTCGACCTCTAGGGTCTCAGGTGATCCTCCCACTTCATCCTTC CACGATCATGGCTCACTGTAGTCTCGACCTCT_GGGTCTCAGGTGATCCTCCCACTTCATCCTTC TA T CFAP161 Ensembl:ENSG00000156206 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202459683 Functional Loss DEL dbSNP153 33..33 33 - - - 48317 RMVar_ID_48317 Human_SNP_ID_585067341 A-to-I Human chr15 - 82010372 82010372 82010372 CACACAATATAGTGAAGATAAAGCCAGGCAAGAGGGAGACTTGGGTTAGATGACCAGAGGGTCCA CACACAATATAGTGAAGATAAAGCCAGGCAAGCGGGAGACTTGGGTTAGATGACCAGAGGGTCCA T G AC104041.1,AC026956.1 Ensembl:ENSG00000259692,Ensembl:ENSG00000259622 lincRNA,Pseudogene intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215560685 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_174324 48318 RMVar_ID_48318 Human_SNP_ID_585075922 A-to-I Human chr15 - 82044493 82044493 82044493 CAGGAAGGAGGATGTGGCCATGGCTCGGAGGGAGATCATCTCTGCTGCCGAGCACTTCTCCATGA CAGGAAGGAGGATGTGGCCATGGCTCGGAGGGGGATCATCTCTGCTGCCGAGCACTTCTCCATGA T C MEX3B Ensembl:ENSG00000183496 Protein coding CDS GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs772755317 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6471982,Human_RBP_ID_22047636,Human_RBP_ID_26438312 48319 RMVar_ID_48319 Human_SNP_ID_585110982 A-to-I Human chr15 - 82181023 82181023 82181023 ATAATTGGTCAATTAAAAAAAAAATTTAGGCCAGGAGCGGTGGCTCACACCTGTAATCCCAGCAC ATAATTGGTCAATTAAAAAAAAAATTTAGGCCGGGAGCGGTGGCTCACACCTGTAATCCCAGCAC T C EFL1 Ensembl:ENSG00000140598 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1381519491 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_117343,RMVar_hsa_circ_113389,RMVar_hsa_circ_12242,RMVar_hsa_circ_174331,RMVar_hsa_circ_373040,RMVar_hsa_circ_97991,RMVar_hsa_circ_174335,RMVar_hsa_circ_9921,RMVar_hsa_circ_174334,RMVar_hsa_circ_18610,RMVar_hsa_circ_174340 48320 RMVar_ID_48320 Human_SNP_ID_585195524 A-to-I Human chr15 - 82544528 82544528 82544528 CCCAAAGCTGGCAGGTCAGGCAAGCAGCCTGCACCACCCTGCCACTGGCGACCAGGGAGCTGGCT CCCAAAGCTGGCAGGTCAGGCAAGCAGCCTGCGCCACCCTGCCACTGGCGACCAGGGAGCTGGCT T C CPEB1,AC245033.1 Ensembl:ENSG00000214575,Ensembl:ENSG00000260836 Protein coding,Protein coding exon,intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs894732095 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106912,RMVar_hsa_circ_174354,RMVar_hsa_circ_174352,RMVar_hsa_circ_92729,RMVar_hsa_circ_114645,RMVar_hsa_circ_174355 48321 RMVar_ID_48321 Human_SNP_ID_585250233 A-to-I Human chr15 - 82743139 82743139 82743139 CTTGTGCCTCAGCCTCACAAGAAGCTGGGACTACAGGCACGCACCACCACCCCCTGCTAATTTTT CTTGTGCCTCAGCCTCACAAGAAGCTGGGACTGCAGGCACGCACCACCACCCCCTGCTAATTTTT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1193134812 Functional Loss SNV dbSNP153 33..33 33 - - - 48322 RMVar_ID_48322 Human_SNP_ID_585251950 A-to-I Human chr15 - 82749145 82749145 82749145 AGGAGGTGGAGGTTGCAGTGAGCTGAGATGGCACCGTTGCACTCCAACCTGGGTGACGAGCGAAA AGGAGGTGGAGGTTGCAGTGAGCTGAGATGGCGCCGTTGCACTCCAACCTGGGTGACGAGCGAAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1363137474 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25172537 48323 RMVar_ID_48323 Human_SNP_ID_585271184 A-to-I Human chr15 + 82825002 82825002 82825002 ACAGTGAGACCTCATCTCTATGGTGCGCACCTATAGTCCCAGCTACTCAAGAGGCTGAGGCAGGA ACAGTGAGACCTCATCTCTATGGTGCGCACCTGTAGTCCCAGCTACTCAAGAGGCTGAGGCAGGA A G WHAMM Ensembl:ENSG00000156232 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1179066592 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48067,RMVar_hsa_circ_314177,RMVar_hsa_circ_285931 48324 RMVar_ID_48324 Human_SNP_ID_585271187 A-to-I Human chr15 + 82825014 82825014 82825014 CATCTCTATGGTGCGCACCTATAGTCCCAGCTACTCAAGAGGCTGAGGCAGGAGGATCGCTTGAA CATCTCTATGGTGCGCACCTATAGTCCCAGCTGCTCAAGAGGCTGAGGCAGGAGGATCGCTTGAA A G WHAMM Ensembl:ENSG00000156232 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1232324134 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_48067,RMVar_hsa_circ_314177,RMVar_hsa_circ_285931 48325 RMVar_ID_48325 Human_SNP_ID_585277982 A-to-I Human chr15 - 82849412 82849412 82849412 TGTTTATATCTTTCATAAGGGCTGTTGCAACCATATGAACTGAAAAAACACGCATTTTGTAATCC TGTTTATATCTTTCATAAGGGCTGTTGCAACCGTATGAACTGAAAAAACACGCATTTTGTAATCC T C HOMER2 Ensembl:ENSG00000103942 Protein coding intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1203128134 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_465662,Human_RBP_ID_1509782,Human_RBP_ID_1835748,Human_RBP_ID_3485341,Human_RBP_ID_6472811,Human_RBP_ID_8802713,Human_RBP_ID_17484124,Human_RBP_ID_27437681 Human_miRNA_ID_1806252 48326 RMVar_ID_48326 Human_SNP_ID_585288777 A-to-I Human chr15 - 82892734 82892734 82892734 GAGCAAGCAGGCGGTCACCGTTTCCTACTTCTATGATGTCACAAGGAACAGCTATCGGATCATCA GAGCAAGCAGGCGGTCACCGTTTCCTACTTCTGTGATGTCACAAGGAACAGCTATCGGATCATCA T C HOMER2 Ensembl:ENSG00000103942 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs759254280 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_465677 Human_Splice_Rec_1637227,Human_Splice_Rec_1637243,Human_Splice_Rec_1637271,Human_Splice_Rec_1637281 RMVar_hsa_circ_174362,RMVar_hsa_circ_174364,RMVar_hsa_circ_287971,RMVar_hsa_circ_366521 48327 RMVar_ID_48327 Human_SNP_ID_585314492 A-to-I Human chr15 - 82999409 82999409 82999409 GGAGGATAGTTTGTGGCCAGGAGTTTGAGACCAGCTTGGGCGACGTGGTAAGACCCCATTTCTCC GGAGGATAGTTTGTGGCCAGGAGTTTGAGACCCGCTTGGGCGACGTGGTAAGACCCCATTTCTCC T G C15orf40 Ensembl:ENSG00000169609 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs951683682 Functional Loss SNV dbSNP153 33..33 33 - - - 48328 RMVar_ID_48328 Human_SNP_ID_585315080 A-to-I Human chr15 - 83002040 83002040 83002040 AGCTGGGCGTGGTGGTACATGACTGTAATCTCAGCTACTTGGGAGGCTGAAGCAGGAGAATTGCT AGCTGGGCGTGGTGGTACATGACTGTAATCTCGGCTACTTGGGAGGCTGAAGCAGGAGAATTGCT T C C15orf40 Ensembl:ENSG00000169609 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs916870007 Functional Loss SNV dbSNP153 33..33 33 - - - 48329 RMVar_ID_48329 Human_SNP_ID_585315467 A-to-I Human chr15 - 83003413 83003413 83003413 ATAAAAGATCAACTTTCCTGGCCGGGCATGGTAGCTCACACCTGTAATCCCAGCACTTTGGGAGG ATAAAAGATCAACTTTCCTGGCCGGGCATGGTCGCTCACACCTGTAATCCCAGCACTTTGGGAGG T G C15orf40 Ensembl:ENSG00000169609 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs977548426 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_465707,Human_RBP_ID_12616435 48330 RMVar_ID_48330 Human_SNP_ID_585316050 A-to-I Human chr15 - 83005409 83005409 83005409 GTGATGGCGCATGCCTGTAATCCCAGTTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCTG GTGATGGCGCATGCCTGTAATCCCAGTTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCTG T C C15orf40 Ensembl:ENSG00000169609 Protein coding intron GSE47997;GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,29129909,29796672,31158229,31158229,32596459,32596459 RNA-Seq:(High) rs1275959286 Functional Loss SNV dbSNP153 33..33 33 - - - 48331 RMVar_ID_48331 Human_SNP_ID_585316064 A-to-I Human chr15 - 83005477 83005477 83005477 GAGTTCGAGACCAGCCTGACCAACATGGTGAAACCCCATCTCTACGAAAAATACAAAATTAGCCA GAGTTCGAGACCAGCCTGACCAACATGGTGAAGCCCCATCTCTACGAAAAATACAAAATTAGCCA T C C15orf40 Ensembl:ENSG00000169609 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs188393349 Functional Loss SNV dbSNP153 33..33 33 - - - 48332 RMVar_ID_48332 Human_SNP_ID_585316103 A-to-I Human chr15 - 83005573 83005573 83005573 AAAACATAAAAGCAAGAAATGAGGCCGGGCGCAGTGGCTCATGCCTGTAATCCCAGCACTTTGGG AAAACATAAAAGCAAGAAATGAGGCCGGGCGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGG T C C15orf40 Ensembl:ENSG00000169609 Protein coding intron GSE38233;GSE100210;GSE107867;GSE107867;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,30559470,30559470,32596459,32596459 RNA-Seq:(High) rs1303616848 Functional Loss SNV dbSNP153 33..33 33 - - - 48333 RMVar_ID_48333 Human_SNP_ID_585316406 A-to-I Human chr15 - 83006669 83006669 83006669 ATCCGCCCCGCGCCCCGCCCCTCCCCGGTTCAAGTGATTCTCCTGCTTCAGCCTCCCGAGTAGCT ATCCGCCCCGCGCCCCGCCCCTCCCCGGTTCAGGTGATTCTCCTGCTTCAGCCTCCCGAGTAGCT T C C15orf40 Ensembl:ENSG00000169609 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1002737935 Functional Loss SNV dbSNP153 33..33 33 - - - 48334 RMVar_ID_48334 Human_SNP_ID_585320786 A-to-I Human chr15 - 83022878 83022878 83022878 TTGGCTCACTGCAATCTCTGCCTCCAGGTTCAAGCGATTCTCCTGCTTCAGCCTCCTGAGTAGCT TTGGCTCACTGCAATCTCTGCCTCCAGGTTCATGCGATTCTCCTGCTTCAGCCTCCTGAGTAGCT T A BTBD1,AC022558.1 Ensembl:ENSG00000064726,Ensembl:ENSG00000259767 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1405909562 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25938,RMVar_hsa_circ_35687,RMVar_hsa_circ_174367,RMVar_hsa_circ_337100,RMVar_hsa_circ_6146,RMVar_hsa_circ_174368 48335 RMVar_ID_48335 Human_SNP_ID_585321025 A-to-I Human chr15 - 83024020 83024020 83024020 ACAAAAAAATATAAAAATTAGCTGAGCATGGTAGCGTGTGCCTGTAGTCCCAGCTACTTGTGGGG ACAAAAAAATATAAAAATTAGCTGAGCATGGTGGCGTGTGCCTGTAGTCCCAGCTACTTGTGGGG T C BTBD1,AC022558.1 Ensembl:ENSG00000064726,Ensembl:ENSG00000259767 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs900598646 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25938,RMVar_hsa_circ_35687,RMVar_hsa_circ_174367,RMVar_hsa_circ_337100,RMVar_hsa_circ_6146,RMVar_hsa_circ_174368 48336 RMVar_ID_48336 Human_SNP_ID_585321178 A-to-I Human chr15 - 83024743 83024743 83024743 TTCAAAAATTCAGCATGGTGGCATGCACCTGTAATCTCAGCTACTTAAGAGGCTGAGGAAGGAGG TTCAAAAATTCAGCATGGTGGCATGCACCTGTCATCTCAGCTACTTAAGAGGCTGAGGAAGGAGG T G BTBD1 Ensembl:ENSG00000064726 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1436131761 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25938,RMVar_hsa_circ_35687,RMVar_hsa_circ_174367,RMVar_hsa_circ_337100,RMVar_hsa_circ_6146,RMVar_hsa_circ_174368 48337 RMVar_ID_48337 Human_SNP_ID_585321305 A-to-I Human chr15 - 83025301 83025301 83025301 CAGGCTGGAGTGCAATGGTGAGATCTGGGCTCACTGCAACCTCCGCCTCCTGAGTTCAAGTAATT CAGGCTGGAGTGCAATGGTGAGATCTGGGCTCGCTGCAACCTCCGCCTCCTGAGTTCAAGTAATT T C BTBD1 Ensembl:ENSG00000064726 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1309881463 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25938,RMVar_hsa_circ_35687,RMVar_hsa_circ_174367,RMVar_hsa_circ_337100,RMVar_hsa_circ_6146,RMVar_hsa_circ_174368 48338 RMVar_ID_48338 Human_SNP_ID_585321711 A-to-I Human chr15 - 83026687 83026687 83026687 AGAAACCCCGTCTCTACTAAAAATACAAAATTAGCCAGGTGTGGGGGCACATGCCTGTAATACCA AGAAACCCCGTCTCTACTAAAAATACAAAATTCGCCAGGTGTGGGGGCACATGCCTGTAATACCA T G BTBD1 Ensembl:ENSG00000064726 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs888593799 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25938,RMVar_hsa_circ_35687,RMVar_hsa_circ_174367,RMVar_hsa_circ_337100,RMVar_hsa_circ_6146,RMVar_hsa_circ_174368 48339 RMVar_ID_48339 Human_SNP_ID_585321857 A-to-I Human chr15 - 83027240 83027240 83027240 TCAAGCGATTCTCCTGCCTCAGGCTCCCAGGTAGCTGGGATTACAGGCATGTGCCACCACACCTG TCAAGCGATTCTCCTGCCTCAGGCTCCCAGGTTGCTGGGATTACAGGCATGTGCCACCACACCTG T A BTBD1 Ensembl:ENSG00000064726 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1430569275 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25938,RMVar_hsa_circ_35687,RMVar_hsa_circ_174367,RMVar_hsa_circ_337100,RMVar_hsa_circ_6146,RMVar_hsa_circ_174368 48340 RMVar_ID_48340 Human_SNP_ID_585325187 A-to-I Human chr15 - 83040555 83040555 83040555 GCTGGGATTACAGGCGTGCACCGCCACAAACTAATTTTTGTATTTTTAGTAGAGACAGAGTTTCA GCTGGGATTACAGGCGTGCACCGCCACAAACTTATTTTTGTATTTTTAGTAGAGACAGAGTTTCA T A BTBD1 Ensembl:ENSG00000064726 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1043191185 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25188733 RMVar_hsa_circ_25938,RMVar_hsa_circ_35687,RMVar_hsa_circ_174367,RMVar_hsa_circ_337100,RMVar_hsa_circ_6146,RMVar_hsa_circ_174368,RMVar_hsa_circ_317793,RMVar_hsa_circ_322202,RMVar_hsa_circ_338570,RMVar_hsa_circ_174369 48341 RMVar_ID_48341 Human_SNP_ID_585325512 A-to-I Human chr15 - 83041481 83041481 83041481 ATCTCAGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACCCAGGAGACGGAGGTTGCAGTG ATCTCAGCTACTCAGGAGGCTGAGGCAGGAGACTCGCTTGAACCCAGGAGACGGAGGTTGCAGTG T G BTBD1 Ensembl:ENSG00000064726 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1444020039 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25938,RMVar_hsa_circ_35687,RMVar_hsa_circ_174367,RMVar_hsa_circ_337100,RMVar_hsa_circ_6146,RMVar_hsa_circ_174368,RMVar_hsa_circ_317793,RMVar_hsa_circ_322202,RMVar_hsa_circ_338570,RMVar_hsa_circ_174369 48342 RMVar_ID_48342 Human_SNP_ID_585328805 A-to-I Human chr15 - 83054181 83054181 83054181 AGTGCGTACCACCACGCCTGGCTAATTTTTTTATTTTGGTAGGAACGGGGTTTCCCCATGTTGGC AGTGCGTACCACCACGCCTGGCTAATTTTTTTGTTTTGGTAGGAACGGGGTTTCCCCATGTTGGC T C BTBD1 Ensembl:ENSG00000064726 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1462874821 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12617094 RMVar_hsa_circ_25938,RMVar_hsa_circ_174367,RMVar_hsa_circ_337100,RMVar_hsa_circ_174368,RMVar_hsa_circ_322202,RMVar_hsa_circ_174369,RMVar_hsa_circ_289316,RMVar_hsa_circ_174372,RMVar_hsa_circ_174373,RMVar_hsa_circ_313916 48343 RMVar_ID_48343 Human_SNP_ID_585328809 A-to-I Human chr15 - 83054190 83054190 83054190 GGGATTACCAGTGCGTACCACCACGCCTGGCTAATTTTTTTATTTTGGTAGGAACGGGGTTTCCC GGGATTACCAGTGCGTACCACCACGCCTGGCTGATTTTTTTATTTTGGTAGGAACGGGGTTTCCC T C BTBD1 Ensembl:ENSG00000064726 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1342879605 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25173107 RMVar_hsa_circ_25938,RMVar_hsa_circ_174367,RMVar_hsa_circ_337100,RMVar_hsa_circ_174368,RMVar_hsa_circ_322202,RMVar_hsa_circ_174369,RMVar_hsa_circ_289316,RMVar_hsa_circ_174372,RMVar_hsa_circ_174373,RMVar_hsa_circ_313916 48344 RMVar_ID_48344 Human_SNP_ID_585330204 A-to-I Human chr15 - 83059651 83059651 83059651 CTGAGCCCAGGAATTTCAGGATACAGTGAGCTATGATCGTGCCACCACTCTCCACCCGGAGTGAC CTGAGCCCAGGAATTTCAGGATACAGTGAGCTGTGATCGTGCCACCACTCTCCACCCGGAGTGAC T C BTBD1 Ensembl:ENSG00000064726 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs944486575 Functional Loss SNV dbSNP153 33..33 33 - - - 48345 RMVar_ID_48345 Human_SNP_ID_585381883 A-to-I Human chr15 - 83270231 83270231 83270231 GATGATGGTTGCATAACTCTGTGAATATGCTAAAAATCATTGAATTGTACACCTTAAATGGGTGA GATGATGGTTGCATAACTCTGTGAATATGCTACAAATCATTGAATTGTACACCTTAAATGGGTGA T G BNC1 Ensembl:ENSG00000169594 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs576187012 Functional Loss SNV dbSNP153 33..33 33 - - - 48346 RMVar_ID_48346 Human_SNP_ID_585433297 A-to-I Human chr15 + 83485532 83485532 83485532 TTGAGGTGGGGTCTTGCTCTGTTGCCCAGGCTAGAGTACAGCAGCATGATCATGGCTCCCTGCAG TTGAGGTGGGGTCTTGCTCTGTTGCCCAGGCTGGAGTACAGCAGCATGATCATGGCTCCCTGCAG A G SH3GL3 Ensembl:ENSG00000140600 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1384658065 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_174390,RMVar_hsa_circ_174391 48347 RMVar_ID_48347 Human_SNP_ID_585670425 A-to-I Human chr15 - 84640613 84640613 84640613 CAGCTCACTGCGGCCTCCAACTCCTGGGCTCAAGTGATTCTCCTGCCCCAGCCTCCCGAGTAGCT CAGCTCACTGCGGCCTCCAACTCCTGGGCTCAGGTGATTCTCCTGCCCCAGCCTCCCGAGTAGCT T C WDR73 Ensembl:ENSG00000177082 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1138785 Functional Loss SNV dbSNP153 33..33 33 - - - 48348 RMVar_ID_48348 Human_SNP_ID_585670684 A-to-I Human chr15 + 84641607 84641601 84641607 ACAATCTCGGTTCACTGCAGCCTCTACCTCTCAGGTTCAAGCAATTCTCCTGCCTCACCCTCCTG ACAATCTCGGTTCACTGCAGCCTCTAC______GGTTCAAGCAATTCTCCTGCCTCACCCTCCTG CCTCTCA C SCAND2P Ensembl:ENSG00000176700 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs746917926 Functional Loss DEL dbSNP153 28..33 33 - - - Human_RBP_ID_124016,Human_RBP_ID_17367280 48349 RMVar_ID_48349 Human_SNP_ID_585670687 A-to-I Human chr15 + 84641607 84641607 84641607 ACAATCTCGGTTCACTGCAGCCTCTACCTCTCAGGTTCAAGCAATTCTCCTGCCTCACCCTCCTG ACAATCTCGGTTCACTGCAGCCTCTACCTCTCGGGTTCAAGCAATTCTCCTGCCTCACCCTCCTG A G SCAND2P Ensembl:ENSG00000176700 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900277457 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_124016,Human_RBP_ID_17367280 48350 RMVar_ID_48350 Human_SNP_ID_585670692 A-to-I Human chr15 + 84641643 84641643 84641643 TCAAGCAATTCTCCTGCCTCACCCTCCTGAGTAGTGGGGATTACAGGTGTGCCACCACCATGCCC TCAAGCAATTCTCCTGCCTCACCCTCCTGAGTGGTGGGGATTACAGGTGTGCCACCACCATGCCC A G SCAND2P Ensembl:ENSG00000176700 Pseudogene exon GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1032698642 Functional Loss SNV dbSNP153 33..33 33 - - - 48351 RMVar_ID_48351 Human_SNP_ID_585670871 A-to-I Human chr15 - 84642218 84642218 84642218 CTCCTGCCTCAGCCTGCCAAGTAGCTGGGATTACAGGCACGTACCACCATGCCCAGGTAATTTTT CTCCTGCCTCAGCCTGCCAAGTAGCTGGGATTGCAGGCACGTACCACCATGCCCAGGTAATTTTT T C WDR73 Ensembl:ENSG00000177082 Protein coding 3'UTR GSE100210;GSE99789;GSE123020:GSM3490829,GSM3490830,GSM3490831 HepG2 cell line;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109 cell line - 29129909,29796672,32596459 RNA-Seq:(High) rs886500952 Functional Loss SNV dbSNP153 33..33 33 - - - 48352 RMVar_ID_48352 Human_SNP_ID_585671003 A-to-I Human chr15 + 84642596 84642596 84642596 TCAGGCAACCCTCCCACCTCAGCCTCTTGAATAGCTGGGACTGCAGGCTCATACCACCACAACCA TCAGGCAACCCTCCCACCTCAGCCTCTTGAATTGCTGGGACTGCAGGCTCATACCACCACAACCA A T SCAND2P Ensembl:ENSG00000176700 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1161919393 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12620058,Human_RBP_ID_18529235 48353 RMVar_ID_48353 Human_SNP_ID_585671012 A-to-I Human chr15 - 84642631 84642631 84642631 GCGAAACCTTGTCTCTACTAAAAATACAAGTTAGCTGGTTGTGGTGGTATGAGCCTGCAGTCCCA GCGAAACCTTGTCTCTACTAAAAATACAAGTTGGCTGGTTGTGGTGGTATGAGCCTGCAGTCCCA T C WDR73,AC048382.7 Ensembl:ENSG00000177082,Ensembl:ENSG00000277578 Protein coding,Other 3'UTR,exon GSE38233;GSE100210;GSE99789;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,29796672,31158229 RNA-Seq:(High) rs901952476 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1176381,Human_RBP_ID_17251447,Human_RBP_ID_26436490 48354 RMVar_ID_48354 Human_SNP_ID_585671013 A-to-I Human chr15 - 84642638 84642638 84642638 CAACATGGCGAAACCTTGTCTCTACTAAAAATACAAGTTAGCTGGTTGTGGTGGTATGAGCCTGC CAACATGGCGAAACCTTGTCTCTACTAAAAATGCAAGTTAGCTGGTTGTGGTGGTATGAGCCTGC T C WDR73,AC048382.7 Ensembl:ENSG00000177082,Ensembl:ENSG00000277578 Protein coding,Other 3'UTR,exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1174893713 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1176381,Human_RBP_ID_17251447 48355 RMVar_ID_48355 Human_SNP_ID_585671023 A-to-I Human chr15 - 84642666 84642666 84642666 GAGTCCAGGAGTTCGAGACTAGCCTGAGCAACATGGCGAAACCTTGTCTCTACTAAAAATACAAG GAGTCCAGGAGTTCGAGACTAGCCTGAGCAACGTGGCGAAACCTTGTCTCTACTAAAAATACAAG T C WDR73,AC048382.7 Ensembl:ENSG00000177082,Ensembl:ENSG00000277578 Protein coding,Other 3'UTR,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1336610388 Functional Loss SNV dbSNP153 33..33 33 - - - 48356 RMVar_ID_48356 Human_SNP_ID_585671057 A-to-I Human chr15 - 84642756 84642756 84642756 TCCCTTAAAAAAAAAAAAAAATTTGGCTGGGCATGGTGGCTCATGCCTGTAATCCCAGCAATGTA TCCCTTAAAAAAAAAAAAAAATTTGGCTGGGCGTGGTGGCTCATGCCTGTAATCCCAGCAATGTA T C WDR73,AC048382.7 Ensembl:ENSG00000177082,Ensembl:ENSG00000277578 Protein coding,Other 3'UTR,exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1041329966 Functional Loss SNV dbSNP153 33..33 33 - - - 48357 RMVar_ID_48357 Human_SNP_ID_585679987 A-to-I Human chr15 - 84674589 84674589 84674589 ACACCACTGCATTCTAGCCTGGGTGCCAGAGTAAGATCATGTATCAAAAAAAAAATTTTTTTTTT ACACCACTGCATTCTAGCCTGGGTGCCAGAGTGAGATCATGTATCAAAAAAAAAATTTTTTTTTT T C SEC11A Ensembl:ENSG00000140612 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1160256454 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_174458,RMVar_hsa_circ_114890,RMVar_hsa_circ_104730,RMVar_hsa_circ_77057,RMVar_hsa_circ_174459,RMVar_hsa_circ_266770,RMVar_hsa_circ_363899,RMVar_hsa_circ_174457,RMVar_hsa_circ_331085,RMVar_hsa_circ_174461 48358 RMVar_ID_48358 Human_SNP_ID_585679995 A-to-I Human chr15 - 84674619 84674618 84674619 AGGAGTTCAAGGCTGTAGTGAGCTATGATCACACCACTGCATTCTAGCCTGGGTGCCAGAGTAAG AGGAGTTCAAGGCTGTAGTGAGCTATGATCAC_CCACTGCATTCTAGCCTGGGTGCCAGAGTAAG GT G SEC11A Ensembl:ENSG00000140612 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1296368614 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_174458,RMVar_hsa_circ_114890,RMVar_hsa_circ_104730,RMVar_hsa_circ_77057,RMVar_hsa_circ_174459,RMVar_hsa_circ_266770,RMVar_hsa_circ_363899,RMVar_hsa_circ_174457,RMVar_hsa_circ_331085,RMVar_hsa_circ_174461 48359 RMVar_ID_48359 Human_SNP_ID_585680669 A-to-I Human chr15 - 84677535 84677535 84677535 CCGGGAGGTGGAGCTTGCAGTGAGCCGAGATCACGCCACTGCACTCCAGCCTGAGTGACAGAGCG CCGGGAGGTGGAGCTTGCAGTGAGCCGAGATCGCGCCACTGCACTCCAGCCTGAGTGACAGAGCG T C SEC11A Ensembl:ENSG00000140612 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs567981309 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25188851 RMVar_hsa_circ_174458,RMVar_hsa_circ_114890,RMVar_hsa_circ_104730,RMVar_hsa_circ_77057,RMVar_hsa_circ_174459,RMVar_hsa_circ_266770,RMVar_hsa_circ_363899,RMVar_hsa_circ_174457,RMVar_hsa_circ_331085,RMVar_hsa_circ_174461 48360 RMVar_ID_48360 Human_SNP_ID_585680670 A-to-I Human chr15 - 84677535 84677535 84677535 CCGGGAGGTGGAGCTTGCAGTGAGCCGAGATCACGCCACTGCACTCCAGCCTGAGTGACAGAGCG CCGGGAGGTGGAGCTTGCAGTGAGCCGAGATCCCGCCACTGCACTCCAGCCTGAGTGACAGAGCG T G SEC11A Ensembl:ENSG00000140612 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs567981309 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25188851 RMVar_hsa_circ_174458,RMVar_hsa_circ_114890,RMVar_hsa_circ_104730,RMVar_hsa_circ_77057,RMVar_hsa_circ_174459,RMVar_hsa_circ_266770,RMVar_hsa_circ_363899,RMVar_hsa_circ_174457,RMVar_hsa_circ_331085,RMVar_hsa_circ_174461 48361 RMVar_ID_48361 Human_SNP_ID_585681030 A-to-I Human chr15 - 84678942 84678942 84678942 CACCCAGGCTAGAGTGTGGGTGGCATGATCTCAGCTCACTGCAACCTCTGCCTCCTGGGCTTAAA CACCCAGGCTAGAGTGTGGGTGGCATGATCTCTGCTCACTGCAACCTCTGCCTCCTGGGCTTAAA T A SEC11A Ensembl:ENSG00000140612 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1254039849 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_174458,RMVar_hsa_circ_114890,RMVar_hsa_circ_104730,RMVar_hsa_circ_77057,RMVar_hsa_circ_174459,RMVar_hsa_circ_266770,RMVar_hsa_circ_363899,RMVar_hsa_circ_174457,RMVar_hsa_circ_331085,RMVar_hsa_circ_174461 48362 RMVar_ID_48362 Human_SNP_ID_585681766 A-to-I Human chr15 - 84681830 84681830 84681830 AAGTGATCCACCCACCCACCTTGGCCTCTTAAAATGCTAGGATTACAGGAGTGAGCCACTGCCCC AAGTGATCCACCCACCCACCTTGGCCTCTTAAGATGCTAGGATTACAGGAGTGAGCCACTGCCCC T C SEC11A Ensembl:ENSG00000140612 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1347646568 Functional Loss SNV dbSNP153 33..33 33 - - - 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_174462,RMVar_hsa_circ_174463 48363 RMVar_ID_48363 Human_SNP_ID_585683539 A-to-I Human chr15 - 84688882 84688882 84688882 GGATTACAGGCGTGCGCCACCATGCTCACCTAATTTTTGTATTTTTAGTTGAGACTGGGTTTCAC GGATTACAGGCGTGCGCCACCATGCTCACCTAGTTTTTGTATTTTTAGTTGAGACTGGGTTTCAC T C SEC11A Ensembl:ENSG00000140612 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1188749288 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12620941 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 48364 RMVar_ID_48364 Human_SNP_ID_585684007 A-to-I Human chr15 - 84690579 84690579 84690579 GGGGTCTCGCTCTGTTACCCAGGATAGAGTGCAGTGGCGCCGTCATAACTCACTGCAGACTCCAC GGGGTCTCGCTCTGTTACCCAGGATAGAGTGCGGTGGCGCCGTCATAACTCACTGCAGACTCCAC T C SEC11A Ensembl:ENSG00000140612 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1368769481 Functional Loss SNV dbSNP153 33..33 33 - - - 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 48365 RMVar_ID_48365 Human_SNP_ID_585684118 A-to-I Human chr15 - 84691081 84691073 84691081 TGACAGAGCGAGACCCTGTCTCCAAAAAAAAAAAAAAAAAGAGAGAAAAGAAATTCTTACTTTGT TGACAGAGCGAGACCCTGTCTCCAAAAAAAAA________GAGAGAAAAGAAATTCTTACTTTGT CTTTTTTTT C SEC11A Ensembl:ENSG00000140612 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs199982469 Functional Loss DEL dbSNP153 33..40 33 - - - 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 48366 RMVar_ID_48366 Human_SNP_ID_585684119 A-to-I Human chr15 - 84691081 84691073 84691081 TGACAGAGCGAGACCCTGTCTCCAAAAAAAAAAAAAAAAAGAGAGAAAAGAAATTCTTACTTTGT TGACAGAGCGAGACCCTGTCTCCAAAAAAAAA___AAAAAGAGAGAAAAGAAATTCTTACTTTGT CTTTTTTTT CTTTTT SEC11A Ensembl:ENSG00000140612 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs199982469 Functional Loss DEL dbSNP153 33..35 33 - - - 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 48367 RMVar_ID_48367 Human_SNP_ID_585684120 A-to-I Human chr15 - 84691081 84691073 84691081 TGACAGAGCGAGACCCTGTCTCCAAAAAAAAAAAAAAAAAGAGAGAAAAGAAATTCTTACTTTGT TGACAGAGCGAGACCCTGTCTCCAAAAAAAAA__AAAAAAGAGAGAAAAGAAATTCTTACTTTGT CTTTTTTTT CTTTTTT SEC11A Ensembl:ENSG00000140612 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs199982469 Functional Loss DEL dbSNP153 33..34 33 - - - 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 48368 RMVar_ID_48368 Human_SNP_ID_585684121 A-to-I Human chr15 - 84691081 84691073 84691081 TGACAGAGCGAGACCCTGTCTCCAAAAAAAAAAAAAAAAAGAGAGAAAAGAAATTCTTACTTTGT TGACAGAGCGAGACCCTGTCTCCAAAAAAAAA_AAAAAAAGAGAGAAAAGAAATTCTTACTTTGT CTTTTTTTT CTTTTTTT SEC11A Ensembl:ENSG00000140612 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs199982469 Functional Loss DEL dbSNP153 33..33 33 - - - 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 48369 RMVar_ID_48369 Human_SNP_ID_585684132 A-to-I Human chr15 - 84691089 84691089 84691089 AGCCTGGGTGACAGAGCGAGACCCTGTCTCCAAAAAAAAAAAAAAAAAGAGAGAAAAGAAATTCT AGCCTGGGTGACAGAGCGAGACCCTGTCTCCAGAAAAAAAAAAAAAAAGAGAGAAAAGAAATTCT T C SEC11A Ensembl:ENSG00000140612 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1291679314 Functional Loss SNV dbSNP153 33..33 33 - - - 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 48370 RMVar_ID_48370 Human_SNP_ID_585684170 A-to-I Human chr15 - 84691268 84691268 84691268 GGAATTTGAGACTAGCTTGGGCAACGTGGTGAAACCCTGTCTCCACAAAAAATACAAAAATTAGC GGAATTTGAGACTAGCTTGGGCAACGTGGTGACACCCTGTCTCCACAAAAAATACAAAAATTAGC T G SEC11A Ensembl:ENSG00000140612 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs79970094 Functional Loss SNV dbSNP153 33..33 33 - - - 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 48371 RMVar_ID_48371 Human_SNP_ID_585685262 A-to-I Human chr15 - 84695600 84695600 84695600 TTGAGACACAGTCTTGCTCTGGCACCTGGGCTAGAATGCAGTGGGGCAATCATAGCTCACTGCAG TTGAGACACAGTCTTGCTCTGGCACCTGGGCTGGAATGCAGTGGGGCAATCATAGCTCACTGCAG T C SEC11A Ensembl:ENSG00000140612 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017807140 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12621085,Human_RBP_ID_18670392 RMVar_hsa_circ_174461,RMVar_hsa_circ_363353 48372 RMVar_ID_48372 Human_SNP_ID_585688677 A-to-I Human chr15 - 84709646 84709646 84709646 TTGAGGTCAGGAGTTCGAAACCAGCCTGGCCAACGTAGTGAAGCCCCGTCTCTACTAAAAATAAA TTGAGGTCAGGAGTTCGAAACCAGCCTGGCCAGCGTAGTGAAGCCCCGTCTCTACTAAAAATAAA T C SEC11A Ensembl:ENSG00000140612 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs908645387 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_174461,RMVar_hsa_circ_363353 48373 RMVar_ID_48373 Human_SNP_ID_585688939 A-to-I Human chr15 - 84710884 84710884 84710884 TATTTTTAGTAGAGACGGGGTTTCACTGTGTTAGCCAGGATGGTCTTGATCTCCTGACCTCGTGA TATTTTTAGTAGAGACGGGGTTTCACTGTGTTCGCCAGGATGGTCTTGATCTCCTGACCTCGTGA T G SEC11A Ensembl:ENSG00000140612 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs998802916 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_174461,RMVar_hsa_circ_363353 48374 RMVar_ID_48374 Human_SNP_ID_585689231 A-to-I Human chr15 - 84711984 84711984 84711984 CTCCCACCTCGGATCCTCAAACTGCTGGAATTACAGATGTGAGCCACCACACCCAGCCAAGTTGT CTCCCACCTCGGATCCTCAAACTGCTGGAATTGCAGATGTGAGCCACCACACCCAGCCAAGTTGT T C SEC11A Ensembl:ENSG00000140612 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1357529031 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12621547 RMVar_hsa_circ_174461,RMVar_hsa_circ_363353 48375 RMVar_ID_48375 Human_SNP_ID_585689501 A-to-I Human chr15 - 84712950 84712950 84712950 CGCCTGCCTCGGCCTTCCAAAATGCTAGGATTACAGGCGTGAGCCACTGCTCCCGGCCGGCCGAT CGCCTGCCTCGGCCTTCCAAAATGCTAGGATTGCAGGCGTGAGCCACTGCTCCCGGCCGGCCGAT T C SEC11A Ensembl:ENSG00000140612 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs569643924 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12621581,Human_RBP_ID_25174367 RMVar_hsa_circ_174461,RMVar_hsa_circ_363353 48376 RMVar_ID_48376 Human_SNP_ID_585691475 A-to-I Human chr15 - 84720408 84720408 84720408 CTCCTGACTCAGCCTCCCGAGTAGCTGGAACTACAGGCATGTGTCCCCACACCTGGCTAATTTTT CTCCTGACTCAGCCTCCCGAGTAGCTGGAACTGCAGGCATGTGTCCCCACACCTGGCTAATTTTT T C AC012291.3 Ensembl:ENSG00000285667 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1292063078 Functional Loss SNV dbSNP153 33..33 33 - - - 48377 RMVar_ID_48377 Human_SNP_ID_585692185 A-to-I Human chr15 - 84723330 84723330 84723330 ACGATCTCGGCTTACTTCAACCTCTGCCTCCCAAGTTCAAATGACTTTCCTGCCTCAGCCTCCCA ACGATCTCGGCTTACTTCAACCTCTGCCTCCCGAGTTCAAATGACTTTCCTGCCTCAGCCTCCCA T C AC012291.3 Ensembl:ENSG00000285667 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264404380 Functional Loss SNV dbSNP153 33..33 33 - - - 48378 RMVar_ID_48378 Human_SNP_ID_585711877 A-to-I Human chr15 + 84797140 84797140 84797140 GTGCCACCATGCCCACTAATTTTTGTATTTTTAGTAGAAACAGGGTTTTGCTATGTCGGCCATGT GTGCCACCATGCCCACTAATTTTTGTATTTTTGGTAGAAACAGGGTTTTGCTATGTCGGCCATGT A G ZNF592 Ensembl:ENSG00000166716 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1002252352 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120468,RMVar_hsa_circ_174467,RMVar_hsa_circ_124655,RMVar_hsa_circ_174466,RMVar_hsa_circ_376202,RMVar_hsa_circ_174468 48379 RMVar_ID_48379 Human_SNP_ID_585788672 A-to-I Human chr15 + 85085752 85085752 85085752 ATGATCGGCTGGGCAGGGTGGCTCACGCCTGTAATCTCTGCACTTTGGGAGGCTGAGGTTGGTGG ATGATCGGCTGGGCAGGGTGGCTCACGCCTGTCATCTCTGCACTTTGGGAGGCTGAGGTTGGTGG A C PDE8A Ensembl:ENSG00000073417 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1044120055 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60082,RMVar_hsa_circ_329617,RMVar_hsa_circ_174475,RMVar_hsa_circ_101353,RMVar_hsa_circ_352461,RMVar_hsa_circ_370821,RMVar_hsa_circ_347470,RMVar_hsa_circ_296713,RMVar_hsa_circ_322322,RMVar_hsa_circ_277134,RMVar_hsa_circ_81492,RMVar_hsa_circ_21935,RMVar_hsa_circ_90249,RMVar_hsa_circ_174479,RMVar_hsa_circ_174481,RMVar_hsa_circ_174482,RMVar_hsa_circ_174480,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_57619,RMVar_hsa_circ_333903,RMVar_hsa_circ_361108,RMVar_hsa_circ_316565,RMVar_hsa_circ_89634,RMVar_hsa_circ_174493,RMVar_hsa_circ_31800,RMVar_hsa_circ_365723,RMVar_hsa_circ_174492,RMVar_hsa_circ_368567,RMVar_hsa_circ_320896,RMVar_hsa_circ_174496,RMVar_hsa_circ_174497 48380 RMVar_ID_48380 Human_SNP_ID_585789071 A-to-I Human chr15 + 85087336 85087336 85087336 GCAGTCCTCCCACCTCAGCTTCTCAAGTAGCTAGGACTACAGATGTATACCACCAGGCCAGCTAA GCAGTCCTCCCACCTCAGCTTCTCAAGTAGCTGGGACTACAGATGTATACCACCAGGCCAGCTAA A G PDE8A Ensembl:ENSG00000073417 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs949216911 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60082,RMVar_hsa_circ_329617,RMVar_hsa_circ_174475,RMVar_hsa_circ_101353,RMVar_hsa_circ_352461,RMVar_hsa_circ_370821,RMVar_hsa_circ_347470,RMVar_hsa_circ_296713,RMVar_hsa_circ_322322,RMVar_hsa_circ_277134,RMVar_hsa_circ_81492,RMVar_hsa_circ_21935,RMVar_hsa_circ_90249,RMVar_hsa_circ_174479,RMVar_hsa_circ_174481,RMVar_hsa_circ_174482,RMVar_hsa_circ_174480,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_57619,RMVar_hsa_circ_333903,RMVar_hsa_circ_361108,RMVar_hsa_circ_316565,RMVar_hsa_circ_89634,RMVar_hsa_circ_174493,RMVar_hsa_circ_31800,RMVar_hsa_circ_365723,RMVar_hsa_circ_174492,RMVar_hsa_circ_368567,RMVar_hsa_circ_320896,RMVar_hsa_circ_174496,RMVar_hsa_circ_174497 48381 RMVar_ID_48381 Human_SNP_ID_585789085 A-to-I Human chr15 + 85087390 85087390 85087390 AGGCCAGCTAATTTTTTATTTTTTGTAGAGACAGGGTTTTGCCATGTTGCCCAGCTGGTCTTGAA AGGCCAGCTAATTTTTTATTTTTTGTAGAGACGGGGTTTTGCCATGTTGCCCAGCTGGTCTTGAA A G PDE8A Ensembl:ENSG00000073417 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs898460606 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60082,RMVar_hsa_circ_329617,RMVar_hsa_circ_174475,RMVar_hsa_circ_101353,RMVar_hsa_circ_352461,RMVar_hsa_circ_370821,RMVar_hsa_circ_347470,RMVar_hsa_circ_296713,RMVar_hsa_circ_322322,RMVar_hsa_circ_277134,RMVar_hsa_circ_81492,RMVar_hsa_circ_21935,RMVar_hsa_circ_90249,RMVar_hsa_circ_174479,RMVar_hsa_circ_174481,RMVar_hsa_circ_174482,RMVar_hsa_circ_174480,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_57619,RMVar_hsa_circ_333903,RMVar_hsa_circ_361108,RMVar_hsa_circ_316565,RMVar_hsa_circ_89634,RMVar_hsa_circ_174493,RMVar_hsa_circ_31800,RMVar_hsa_circ_365723,RMVar_hsa_circ_174492,RMVar_hsa_circ_368567,RMVar_hsa_circ_320896,RMVar_hsa_circ_174496,RMVar_hsa_circ_174497 48382 RMVar_ID_48382 Human_SNP_ID_585789086 A-to-I Human chr15 + 85087390 85087390 85087390 AGGCCAGCTAATTTTTTATTTTTTGTAGAGACAGGGTTTTGCCATGTTGCCCAGCTGGTCTTGAA AGGCCAGCTAATTTTTTATTTTTTGTAGAGACTGGGTTTTGCCATGTTGCCCAGCTGGTCTTGAA A T PDE8A Ensembl:ENSG00000073417 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs898460606 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60082,RMVar_hsa_circ_329617,RMVar_hsa_circ_174475,RMVar_hsa_circ_101353,RMVar_hsa_circ_352461,RMVar_hsa_circ_370821,RMVar_hsa_circ_347470,RMVar_hsa_circ_296713,RMVar_hsa_circ_322322,RMVar_hsa_circ_277134,RMVar_hsa_circ_81492,RMVar_hsa_circ_21935,RMVar_hsa_circ_90249,RMVar_hsa_circ_174479,RMVar_hsa_circ_174481,RMVar_hsa_circ_174482,RMVar_hsa_circ_174480,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_57619,RMVar_hsa_circ_333903,RMVar_hsa_circ_361108,RMVar_hsa_circ_316565,RMVar_hsa_circ_89634,RMVar_hsa_circ_174493,RMVar_hsa_circ_31800,RMVar_hsa_circ_365723,RMVar_hsa_circ_174492,RMVar_hsa_circ_368567,RMVar_hsa_circ_320896,RMVar_hsa_circ_174496,RMVar_hsa_circ_174497 48383 RMVar_ID_48383 Human_SNP_ID_585791195 A-to-I Human chr15 + 85095447 85095447 85095447 CTCACTGCAACCTCTGCCTCTCGGGTTGAAGCAATTCTCCTGCCCCAGCCTCCTGAGTAGCTGGG CTCACTGCAACCTCTGCCTCTCGGGTTGAAGCCATTCTCCTGCCCCAGCCTCCTGAGTAGCTGGG A C PDE8A Ensembl:ENSG00000073417 Protein coding intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs576385312 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60082,RMVar_hsa_circ_329617,RMVar_hsa_circ_174475,RMVar_hsa_circ_101353,RMVar_hsa_circ_352461,RMVar_hsa_circ_370821,RMVar_hsa_circ_322322,RMVar_hsa_circ_277134,RMVar_hsa_circ_81492,RMVar_hsa_circ_90249,RMVar_hsa_circ_174479,RMVar_hsa_circ_174481,RMVar_hsa_circ_174480,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_361108,RMVar_hsa_circ_316565,RMVar_hsa_circ_89634,RMVar_hsa_circ_174493,RMVar_hsa_circ_365723,RMVar_hsa_circ_174492,RMVar_hsa_circ_368567,RMVar_hsa_circ_320896,RMVar_hsa_circ_72645,RMVar_hsa_circ_4057,RMVar_hsa_circ_174497,RMVar_hsa_circ_36056,RMVar_hsa_circ_318408,RMVar_hsa_circ_16470,RMVar_hsa_circ_174498 48384 RMVar_ID_48384 Human_SNP_ID_585801180 A-to-I Human chr15 + 85135315 85135315 85135315 AAGTGGTTAGCCTTTCTTCTGTGCACTCAGCTACCCTTCTCCCTTACCACACCTGGCCCAACACC AAGTGGTTAGCCTTTCTTCTGTGCACTCAGCTGCCCTTCTCCCTTACCACACCTGGCCCAACACC A G PDE8A Ensembl:ENSG00000073417 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs570997325 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102922,RMVar_hsa_circ_174510 48385 RMVar_ID_48385 Human_SNP_ID_585819545 A-to-I Human chr15 + 85213124 85213124 85213124 GCTAATTGTCATCTACCCGCCTCAGCTTCCCAAACTGTTTGGATTACAGGTATGAGCCACTGTGC GCTAATTGTCATCTACCCGCCTCAGCTTCCCAGACTGTTTGGATTACAGGTATGAGCCACTGTGC A G CSPG4P12 Ensembl:ENSG00000259295 Pseudogene exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1351728285 Functional Loss SNV dbSNP153 33..33 33 - - - 48386 RMVar_ID_48386 Human_SNP_ID_585916342 A-to-I Human chr15 + 85579295 85579295 85579295 AGCTGCCTTCAGAGCTTGCCTGATTGTGGAGTAAAGGGCACGGAAGGCCTTTCGTCCTGTGGAAA AGCTGCCTTCAGAGCTTGCCTGATTGTGGAGTTAAGGGCACGGAAGGCCTTTCGTCCTGTGGAAA A T AKAP13 Ensembl:ENSG00000170776 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs778479525 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4337870,Human_RBP_ID_5523802,Human_RBP_ID_6476190,Human_RBP_ID_8802823,Human_RBP_ID_9371215,Human_RBP_ID_18670623 RMVar_hsa_circ_113907,RMVar_hsa_circ_97471,RMVar_hsa_circ_174515,RMVar_hsa_circ_174516,RMVar_hsa_circ_375212,RMVar_hsa_circ_356482,RMVar_hsa_circ_85010,RMVar_hsa_circ_103712,RMVar_hsa_circ_174520,RMVar_hsa_circ_174521,RMVar_hsa_circ_351089,RMVar_hsa_circ_352600,RMVar_hsa_circ_76422,RMVar_hsa_circ_174522,RMVar_hsa_circ_66943,RMVar_hsa_circ_50656,RMVar_hsa_circ_55870,RMVar_hsa_circ_174524,RMVar_hsa_circ_296216,RMVar_hsa_circ_174525,RMVar_hsa_circ_35283,RMVar_hsa_circ_327723 48387 RMVar_ID_48387 Human_SNP_ID_585944562 A-to-I Human chr15 + 85679057 85679057 85679057 GGTCGGGAGTTCAAGACCAGTCTGGCCAACATAGTGAAACCCCATCTCTACCAAAAATACAAAAA GGTCGGGAGTTCAAGACCAGTCTGGCCAACATTGTGAAACCCCATCTCTACCAAAAATACAAAAA A T AKAP13 Ensembl:ENSG00000170776 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1247449082 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85010,RMVar_hsa_circ_103712,RMVar_hsa_circ_174521,RMVar_hsa_circ_174522,RMVar_hsa_circ_174530,RMVar_hsa_circ_55870,RMVar_hsa_circ_55274,RMVar_hsa_circ_93314,RMVar_hsa_circ_174526,RMVar_hsa_circ_68663,RMVar_hsa_circ_63073,RMVar_hsa_circ_279996,RMVar_hsa_circ_329837,RMVar_hsa_circ_349136,RMVar_hsa_circ_104505,RMVar_hsa_circ_19695,RMVar_hsa_circ_174531,RMVar_hsa_circ_8530,RMVar_hsa_circ_65003,RMVar_hsa_circ_174529,RMVar_hsa_circ_268046,RMVar_hsa_circ_365722,RMVar_hsa_circ_325342,RMVar_hsa_circ_350318,RMVar_hsa_circ_300388,RMVar_hsa_circ_319469,RMVar_hsa_circ_320043,RMVar_hsa_circ_323038,RMVar_hsa_circ_310958,RMVar_hsa_circ_174537,RMVar_hsa_circ_174538,RMVar_hsa_circ_270795,RMVar_hsa_circ_351978,RMVar_hsa_circ_364602,RMVar_hsa_circ_45380,RMVar_hsa_circ_174539,RMVar_hsa_circ_174540 48388 RMVar_ID_48388 Human_SNP_ID_585961008 A-to-I Human chr15 + 85737767 85737767 85737767 TCAAGCAATTCTCCTGCCTCGGCCTCCAGAGTAGCTGGGACTACAGGCCCGCACTACCATACCTG TCAAGCAATTCTCCTGCCTCGGCCTCCAGAGTCGCTGGGACTACAGGCCCGCACTACCATACCTG A C AKAP13 Ensembl:ENSG00000170776 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs975458017 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58355,RMVar_hsa_circ_57898,RMVar_hsa_circ_356246,RMVar_hsa_circ_58374 48389 RMVar_ID_48389 Human_SNP_ID_586753602 A-to-I Human chr15 + 88480369 88480369 88480369 CCTGTGAGCATCTGGGACTACAGGCGCATGCCACCACACATGGATAATTTTTGTATTTTTTGTAT CCTGTGAGCATCTGGGACTACAGGCGCATGCCGCCACACATGGATAATTTTTGTATTTTTTGTAT A G MRPS11 Ensembl:ENSG00000181991 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1312585193 Functional Loss SNV dbSNP153 33..33 33 - - - 48390 RMVar_ID_48390 Human_SNP_ID_586759150 A-to-I Human chr15 - 88503155 88503155 88503155 GACTTAAGCGATTCTCATGCCCCAGTCTCCCAAGTAGCTGGGATTACAGGCATGTGCCACCACTC GACTTAAGCGATTCTCATGCCCCAGTCTCCCAGGTAGCTGGGATTACAGGCATGTGCCACCACTC T C DET1,AC013489.1 Ensembl:ENSG00000140543,Ensembl:ENSG00000173867 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005427185 Functional Loss SNV dbSNP153 33..33 33 - - - 48391 RMVar_ID_48391 Human_SNP_ID_586759158 A-to-I Human chr15 - 88503188 88503188 88503188 TGAGATCTCAGCTCTTGCAACCGCCGCCTCCCAGACTTAAGCGATTCTCATGCCCCAGTCTCCCA TGAGATCTCAGCTCTTGCAACCGCCGCCTCCCCGACTTAAGCGATTCTCATGCCCCAGTCTCCCA T G DET1,AC013489.1 Ensembl:ENSG00000140543,Ensembl:ENSG00000173867 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1187915596 Functional Loss SNV dbSNP153 33..33 33 - - - 48392 RMVar_ID_48392 Human_SNP_ID_586800720 A-to-I Human chr15 + 88642066 88642063 88642066 AGCGATTTTCCCGCCTCAGCCTCCCAAGTTGTAGTATAGGTGTCCGCCACCACGCCTGGCTAATT AGCGATTTTCCCGCCTCAGCCTCCCAAGTT___GTATAGGTGTCCGCCACCACGCCTGGCTAATT TGTA T ISG20 Ensembl:ENSG00000172183 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1346213903 Functional Loss DEL dbSNP153 31..33 33 - - - 48393 RMVar_ID_48393 Human_SNP_ID_586800916 A-to-I Human chr15 + 88642800 88642800 88642800 CACCACGCCTGGCTAATTTTTGTATTTTCAGTAGAGACGGGGTTTCACCATGTTGCCAGGCTGGT CACCACGCCTGGCTAATTTTTGTATTTTCAGTGGAGACGGGGTTTCACCATGTTGCCAGGCTGGT A G ISG20 Ensembl:ENSG00000172183 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1465334463 Functional Loss SNV dbSNP153 33..33 33 - - - 48394 RMVar_ID_48394 Human_SNP_ID_586800934 A-to-I Human chr15 + 88642850 88642850 88642850 TGTTGCCAGGCTGGTCTCGAATGCCTCACCTCAAGTGATCCACCCACCTCAGCCTCCCAGAGTGC TGTTGCCAGGCTGGTCTCGAATGCCTCACCTCGAGTGATCCACCCACCTCAGCCTCCCAGAGTGC A G ISG20 Ensembl:ENSG00000172183 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1315902496 Functional Loss SNV dbSNP153 33..33 33 - - - 48395 RMVar_ID_48395 Human_SNP_ID_586801274 A-to-I Human chr15 + 88644347 88644347 88644347 CCAGAGGTCGGGAGTTTGAGATCAGCCTGGCTAACATGGTGAAACCCCGTCTCTACTAAATATAC CCAGAGGTCGGGAGTTTGAGATCAGCCTGGCTGACATGGTGAAACCCCGTCTCTACTAAATATAC A G ISG20 Ensembl:ENSG00000172183 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1467858039 Functional Loss SNV dbSNP153 33..33 33 - - - 48396 RMVar_ID_48396 Human_SNP_ID_586874698 A-to-I Human chr15 - 88905776 88905776 88905776 TGCCACACGGCCTGCACTCTGCGCTTTGAGCTACTGGGCTGTGAGCTGAACGGTGAGTGCTGGGG TGCCACACGGCCTGCACTCTGCGCTTTGAGCTGCTGGGCTGTGAGCTGAACGGTGAGTGCTGGGG T C MFGE8 Ensembl:ENSG00000140545 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1466204236 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4338377,Human_RBP_ID_22426210,Human_RBP_ID_22758966,Human_RBP_ID_23673156 Human_Splice_Rec_1641109,Human_Splice_Rec_1641123,Human_Splice_Rec_1641137,Human_Splice_Rec_1641149,Human_Splice_Rec_1641167,Human_Splice_Rec_1641181,Human_Splice_Rec_1641185 RMVar_hsa_circ_376193,RMVar_hsa_circ_174603 48397 RMVar_ID_48397 Human_SNP_ID_586898826 A-to-I Human chr15 - 88989952 88989952 88989952 AACATTACCCGAATGGAGTCTGCACTGCGTATAGCAAAAAAAAAAAATAGATGGACAGCAAACCA AACATTACCCGAATGGAGTCTGCACTGCGTATGGCAAAAAAAAAAAATAGATGGACAGCAAACCA T C AC107954.1 Ensembl:ENSG00000261549 Pseudogene exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1239049224 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17689282,Human_RBP_ID_26438810 Human_miRNA_ID_1823012 48398 RMVar_ID_48398 Human_SNP_ID_586955038 A-to-I Human chr15 - 89201238 89201238 89201238 GGAGAAATGATGAAGCTATCAGAAGCAAATCAACACCTGAGAGATGAAGGTTTAAGGCTCAGAAA GGAGAAATGATGAAGCTATCAGAAGCAAATCAGCACCTGAGAGATGAAGGTTTAAGGCTCAGAAA T C AC124068.1 Ensembl:ENSG00000259948 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1221058526 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5567821 Human_miRNA_ID_1839307 48399 RMVar_ID_48399 Human_SNP_ID_586955039 A-to-I Human chr15 - 89201239 89201239 89201239 GGGAGAAATGATGAAGCTATCAGAAGCAAATCAACACCTGAGAGATGAAGGTTTAAGGCTCAGAA GGGAGAAATGATGAAGCTATCAGAAGCAAATCGACACCTGAGAGATGAAGGTTTAAGGCTCAGAA T C AC124068.1 Ensembl:ENSG00000259948 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs919896047 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5567821 Human_miRNA_ID_1839307 48400 RMVar_ID_48400 Human_SNP_ID_586955100 A-to-I Human chr15 + 89201496 89201496 89201496 CATTCCACACAGCTTCCATATCTGAAGTGTTTAGTGGAGCAAAAATTGTACCATAAACTTGTGTT CATTCCACACAGCTTCCATATCTGAAGTGTTTGGTGGAGCAAAAATTGTACCATAAACTTGTGTT A G ABHD2 Ensembl:ENSG00000140526 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1330636807 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267600 48401 RMVar_ID_48401 Human_SNP_ID_586969328 A-to-I Human chr15 + 89252476 89252476 89252476 AGTAGCATTCATACATAATAGCCAGTTAGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAG AGTAGCATTCATACATAATAGCCAGTTAGCTCTCGCCTGTAATCCCAGCACTTTGGGAGGCCAAG A T FANCI Ensembl:ENSG00000140525 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1184794095 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16476,RMVar_hsa_circ_56441,RMVar_hsa_circ_106702,RMVar_hsa_circ_174631,RMVar_hsa_circ_174630,RMVar_hsa_circ_174629,RMVar_hsa_circ_338925,RMVar_hsa_circ_273937,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_174633,RMVar_hsa_circ_174635,RMVar_hsa_circ_11881,RMVar_hsa_circ_174634,RMVar_hsa_circ_174632 48402 RMVar_ID_48402 Human_SNP_ID_586970019 A-to-I Human chr15 + 89254622 89254622 89254622 GTCCAGGAGTTTGAGACCAGCTTGGACAACATAGTGAGAACCCACCTCTACAAAAAAATAATTTA GTCCAGGAGTTTGAGACCAGCTTGGACAACATGGTGAGAACCCACCTCTACAAAAAAATAATTTA A G FANCI Ensembl:ENSG00000140525 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041689430 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8425318,Human_RBP_ID_12629531 RMVar_hsa_circ_16476,RMVar_hsa_circ_56441,RMVar_hsa_circ_106702,RMVar_hsa_circ_174631,RMVar_hsa_circ_174630,RMVar_hsa_circ_174629,RMVar_hsa_circ_338925,RMVar_hsa_circ_273937,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_174633,RMVar_hsa_circ_174635,RMVar_hsa_circ_11881,RMVar_hsa_circ_174634,RMVar_hsa_circ_174632 48403 RMVar_ID_48403 Human_SNP_ID_586973913 A-to-I Human chr15 + 89267820 89267820 89267820 ATAGTGGCACATGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGTGGGAGGATCGTTTGAGCCTG ATAGTGGCACATGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGTGGGAGGATCGTTTGAGCCTG A G FANCI Ensembl:ENSG00000140525 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1275209316 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16476,RMVar_hsa_circ_56441,RMVar_hsa_circ_351176,RMVar_hsa_circ_349689,RMVar_hsa_circ_32252,RMVar_hsa_circ_44177,RMVar_hsa_circ_50617,RMVar_hsa_circ_33118,RMVar_hsa_circ_19539,RMVar_hsa_circ_17057,RMVar_hsa_circ_12328,RMVar_hsa_circ_68986,RMVar_hsa_circ_363315,RMVar_hsa_circ_174635,RMVar_hsa_circ_11881,RMVar_hsa_circ_366788,RMVar_hsa_circ_339324,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_38038,RMVar_hsa_circ_31865,RMVar_hsa_circ_64160,RMVar_hsa_circ_174638,RMVar_hsa_circ_43937,RMVar_hsa_circ_337839,RMVar_hsa_circ_174641,RMVar_hsa_circ_51242,RMVar_hsa_circ_118555,RMVar_hsa_circ_174642 48404 RMVar_ID_48404 Human_SNP_ID_586981958 A-to-I Human chr15 + 89295256 89295256 89295256 TAGCCAGGTGGCAGGCACTTGTAATCCCAGCTACTCAGGAAGCTGAGGCAAGAGAATCACTTGAA TAGCCAGGTGGCAGGCACTTGTAATCCCAGCTGCTCAGGAAGCTGAGGCAAGAGAATCACTTGAA A G FANCI Ensembl:ENSG00000140525 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1293724301 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18670992,Human_RBP_ID_22581300 RMVar_hsa_circ_32252,RMVar_hsa_circ_44177,RMVar_hsa_circ_50617,RMVar_hsa_circ_68986,RMVar_hsa_circ_10222,RMVar_hsa_circ_118555,RMVar_hsa_circ_174642,RMVar_hsa_circ_29928,RMVar_hsa_circ_94123,RMVar_hsa_circ_174646,RMVar_hsa_circ_2937,RMVar_hsa_circ_44903,RMVar_hsa_circ_347382,RMVar_hsa_circ_26586 48405 RMVar_ID_48405 Human_SNP_ID_586982040 A-to-I Human chr15 + 89295446 89295446 89295446 CCAGCACTTTGGGAGGCTGAGCCGGGTGGATTACCTGAGGTTGGGAGTTCGAGACCAGTCTGACC CCAGCACTTTGGGAGGCTGAGCCGGGTGGATTTCCTGAGGTTGGGAGTTCGAGACCAGTCTGACC A T FANCI Ensembl:ENSG00000140525 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1205377174 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32252,RMVar_hsa_circ_44177,RMVar_hsa_circ_50617,RMVar_hsa_circ_68986,RMVar_hsa_circ_10222,RMVar_hsa_circ_118555,RMVar_hsa_circ_174642,RMVar_hsa_circ_29928,RMVar_hsa_circ_94123,RMVar_hsa_circ_174646,RMVar_hsa_circ_2937,RMVar_hsa_circ_44903,RMVar_hsa_circ_347382,RMVar_hsa_circ_26586 48406 RMVar_ID_48406 Human_SNP_ID_586982208 A-to-I Human chr15 + 89295810 89295810 89295810 TTTTTTGGCTTTTTTTGAGAGAGTCTCGCTCTATTGCCCAGGGTGGAATGCCGTGGTGCAATCTC TTTTTTGGCTTTTTTTGAGAGAGTCTCGCTCTCTTGCCCAGGGTGGAATGCCGTGGTGCAATCTC A C FANCI Ensembl:ENSG00000140525 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs77539815 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12630651,Human_RBP_ID_25176837 RMVar_hsa_circ_32252,RMVar_hsa_circ_44177,RMVar_hsa_circ_50617,RMVar_hsa_circ_68986,RMVar_hsa_circ_10222,RMVar_hsa_circ_118555,RMVar_hsa_circ_174642,RMVar_hsa_circ_29928,RMVar_hsa_circ_94123,RMVar_hsa_circ_174646,RMVar_hsa_circ_2937,RMVar_hsa_circ_44903,RMVar_hsa_circ_347382,RMVar_hsa_circ_26586 48407 RMVar_ID_48407 Human_SNP_ID_586982209 A-to-I Human chr15 + 89295810 89295810 89295810 TTTTTTGGCTTTTTTTGAGAGAGTCTCGCTCTATTGCCCAGGGTGGAATGCCGTGGTGCAATCTC TTTTTTGGCTTTTTTTGAGAGAGTCTCGCTCTGTTGCCCAGGGTGGAATGCCGTGGTGCAATCTC A G FANCI Ensembl:ENSG00000140525 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs77539815 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12630651,Human_RBP_ID_25176837 RMVar_hsa_circ_32252,RMVar_hsa_circ_44177,RMVar_hsa_circ_50617,RMVar_hsa_circ_68986,RMVar_hsa_circ_10222,RMVar_hsa_circ_118555,RMVar_hsa_circ_174642,RMVar_hsa_circ_29928,RMVar_hsa_circ_94123,RMVar_hsa_circ_174646,RMVar_hsa_circ_2937,RMVar_hsa_circ_44903,RMVar_hsa_circ_347382,RMVar_hsa_circ_26586 48408 RMVar_ID_48408 Human_SNP_ID_586982210 A-to-I Human chr15 + 89295810 89295810 89295810 TTTTTTGGCTTTTTTTGAGAGAGTCTCGCTCTATTGCCCAGGGTGGAATGCCGTGGTGCAATCTC TTTTTTGGCTTTTTTTGAGAGAGTCTCGCTCTTTTGCCCAGGGTGGAATGCCGTGGTGCAATCTC A T FANCI Ensembl:ENSG00000140525 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs77539815 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12630651,Human_RBP_ID_25176837 RMVar_hsa_circ_32252,RMVar_hsa_circ_44177,RMVar_hsa_circ_50617,RMVar_hsa_circ_68986,RMVar_hsa_circ_10222,RMVar_hsa_circ_118555,RMVar_hsa_circ_174642,RMVar_hsa_circ_29928,RMVar_hsa_circ_94123,RMVar_hsa_circ_174646,RMVar_hsa_circ_2937,RMVar_hsa_circ_44903,RMVar_hsa_circ_347382,RMVar_hsa_circ_26586 48409 RMVar_ID_48409 Human_SNP_ID_586982223 A-to-I Human chr15 + 89295851 89295851 89295851 GGTGGAATGCCGTGGTGCAATCTCGGCTCACTACAACCCCTTCCTCCGAGGTTCAAGCAGTCCTT GGTGGAATGCCGTGGTGCAATCTCGGCTCACTGCAACCCCTTCCTCCGAGGTTCAAGCAGTCCTT A G FANCI Ensembl:ENSG00000140525 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1261909431 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32252,RMVar_hsa_circ_44177,RMVar_hsa_circ_50617,RMVar_hsa_circ_68986,RMVar_hsa_circ_10222,RMVar_hsa_circ_118555,RMVar_hsa_circ_174642,RMVar_hsa_circ_29928,RMVar_hsa_circ_94123,RMVar_hsa_circ_174646,RMVar_hsa_circ_2937,RMVar_hsa_circ_44903,RMVar_hsa_circ_347382,RMVar_hsa_circ_26586 48410 RMVar_ID_48410 Human_SNP_ID_586982283 A-to-I Human chr15 + 89296067 89296067 89296067 TTGGCTTACTGCAACCTCGGCCTCCCCGGTTCAAGTGATCCTCCTGCCTCAGTCTCCCAAGTAGC TTGGCTTACTGCAACCTCGGCCTCCCCGGTTCCAGTGATCCTCCTGCCTCAGTCTCCCAAGTAGC A C FANCI Ensembl:ENSG00000140525 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348753129 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32252,RMVar_hsa_circ_44177,RMVar_hsa_circ_50617,RMVar_hsa_circ_68986,RMVar_hsa_circ_10222,RMVar_hsa_circ_118555,RMVar_hsa_circ_174642,RMVar_hsa_circ_29928,RMVar_hsa_circ_94123,RMVar_hsa_circ_174646,RMVar_hsa_circ_2937,RMVar_hsa_circ_44903,RMVar_hsa_circ_347382,RMVar_hsa_circ_26586 48411 RMVar_ID_48411 Human_SNP_ID_587067287 A-to-I Human chr15 + 89591257 89591257 89591257 AAGCTTCTCCTGCCTGAACCTCCCGAATAGCTAGGAATACAGGCACCTGCCACCACGCCCAGCTA AAGCTTCTCCTGCCTGAACCTCCCGAATAGCTGGGAATACAGGCACCTGCCACCACGCCCAGCTA A G AC013391.2,TICRR Ensembl:ENSG00000259713,Ensembl:ENSG00000140534 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1257958759 Functional Loss SNV dbSNP153 33..33 33 - - - 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 48412 RMVar_ID_48412 Human_SNP_ID_587074973 A-to-I Human chr15 - 89619750 89619750 89619750 CAGAATAGAAGGAGGCAGAATGTGTCCTGCTAAATGACAACTGCTTGATTCGAGGACTTCGTCTC CAGAATAGAAGGAGGCAGAATGTGTCCTGCTACATGACAACTGCTTGATTCGAGGACTTCGTCTC T G KIF7 Ensembl:ENSG00000166813 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1319483774 Functional Loss SNV dbSNP153 33..33 33 - - - 48413 RMVar_ID_48413 Human_SNP_ID_587096311 A-to-I Human chr15 - 89688664 89688664 89688664 CATTTAGGCCGGGTTCAGTGACTCACACCTGTAGTCCCAGCACTTTGGGAGGCTGAGGTGGGCAG CATTTAGGCCGGGTTCAGTGACTCACACCTGTGGTCCCAGCACTTTGGGAGGCTGAGGTGGGCAG T C PEX11A Ensembl:ENSG00000166821 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1269562584 Functional Loss SNV dbSNP153 33..33 33 - - - 48414 RMVar_ID_48414 Human_SNP_ID_587135887 A-to-I Human chr15 - 89832187 89832187 89832187 TCCCGCCTTGGCCTCCCAAACATGTTGGGATTACAGGTGTGAGCCACTGGACCTGGCCAAATACT TCCCGCCTTGGCCTCCCAAACATGTTGGGATTGCAGGTGTGAGCCACTGGACCTGGCCAAATACT T C AP3S2 Ensembl:ENSG00000157823 Protein coding 3'UTR GSE38233;GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;ASD brains,temporal_cortex;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,30559470,31158229,31158229,32596459 RNA-Seq:(High) rs1465156466 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26437860 Human_miRNA_ID_2450757,Human_miRNA_ID_2450758 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 48415 RMVar_ID_48415 Human_SNP_ID_587135906 A-to-I Human chr15 - 89832262 89832262 89832262 GTTTTATTTTTTTAGTAGAATAAGGTCTCACTATGTTGCACAGGCTGGTCTCTAACTCCTTACCT GTTTTATTTTTTTAGTAGAATAAGGTCTCACTGTGTTGCACAGGCTGGTCTCTAACTCCTTACCT T C AP3S2 Ensembl:ENSG00000157823 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-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 48416 RMVar_ID_48416 Human_SNP_ID_587135937 A-to-I Human chr15 - 89832406 89832406 89832406 GGGGTCTCACACTGTGGCTCAGGCTGGAGTGCAGTGGTGTGATCATGGCTCACTGCAGCCTCGAA GGGGTCTCACACTGTGGCTCAGGCTGGAGTGCGGTGGTGTGATCATGGCTCACTGCAGCCTCGAA T C AP3S2 Ensembl:ENSG00000157823 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1468324672 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 48417 RMVar_ID_48417 Human_SNP_ID_587136018 A-to-I Human chr15 - 89832613 89832613 89832613 GTGGTAGTGGACACCTGTAGTCCCAGCTACTCAGGAGGCTGCGGCAGGAGAATGGCATGAACCCG GTGGTAGTGGACACCTGTAGTCCCAGCTACTCGGGAGGCTGCGGCAGGAGAATGGCATGAACCCG T C AP3S2 Ensembl:ENSG00000157823 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1472772198 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26436835 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 48418 RMVar_ID_48418 Human_SNP_ID_587136497 A-to-I Human chr15 - 89834837 89834837 89834837 GGAGTGCTGTGGTGCAATCTCGGCTCACTGCAACCTCTGCTTCCCGGGTTCAAGCATTTCTCCTG GGAGTGCTGTGGTGCAATCTCGGCTCACTGCAGCCTCTGCTTCCCGGGTTCAAGCATTTCTCCTG T C AP3S2,ARPIN-AP3S2 Ensembl:ENSG00000157823,Ensembl:ENSG00000250021 Protein coding,Protein coding 3'UTR,3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1175886553 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 48419 RMVar_ID_48419 Human_SNP_ID_587136543 A-to-I Human chr15 - 89834982 89834982 89834982 GTGTGGTGAGTGGCAAGTAAGGGCAGAATTTTAGGAGAACCAGAGTCACCCGCTGGCTCTACTGA GTGTGGTGAGTGGCAAGTAAGGGCAGAATTTTTGGAGAACCAGAGTCACCCGCTGGCTCTACTGA T A AP3S2,ARPIN-AP3S2 Ensembl:ENSG00000157823,Ensembl:ENSG00000250021 Protein coding,Protein coding 3'UTR,3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs950308309 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_466655,Human_RBP_ID_814981,Human_RBP_ID_4339336,Human_RBP_ID_6478618,Human_RBP_ID_12633371,Human_RBP_ID_17868992,Human_RBP_ID_26437869 Human_miRNA_ID_2784403,Human_miRNA_ID_2784404 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 48420 RMVar_ID_48420 Human_SNP_ID_587136544 A-to-I Human chr15 - 89834982 89834982 89834982 GTGTGGTGAGTGGCAAGTAAGGGCAGAATTTTAGGAGAACCAGAGTCACCCGCTGGCTCTACTGA GTGTGGTGAGTGGCAAGTAAGGGCAGAATTTTGGGAGAACCAGAGTCACCCGCTGGCTCTACTGA T C AP3S2,ARPIN-AP3S2 Ensembl:ENSG00000157823,Ensembl:ENSG00000250021 Protein coding,Protein coding 3'UTR,3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs950308309 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_466655,Human_RBP_ID_814981,Human_RBP_ID_4339336,Human_RBP_ID_6478618,Human_RBP_ID_12633371,Human_RBP_ID_17868992,Human_RBP_ID_26437869 Human_miRNA_ID_2784403,Human_miRNA_ID_2784404 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 48421 RMVar_ID_48421 Human_SNP_ID_587153226 A-to-I Human chr15 - 89895994 89895994 89895994 ATCCCAGCTACTGGGGAGGCTGAAGCAGGAGAATTGTTTGAACCCGGGAGACGGAGGTTGCAGTG ATCCCAGCTACTGGGGAGGCTGAAGCAGGAGAGTTGTTTGAACCCGGGAGACGGAGGTTGCAGTG T C ARPIN,ARPIN-AP3S2 Ensembl:ENSG00000242498,Ensembl:ENSG00000250021 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs540085842 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_347469,RMVar_hsa_circ_56287 48422 RMVar_ID_48422 Human_SNP_ID_587153486 A-to-I Human chr15 - 89897268 89897265 89897268 GTCAGCCAGGCTTTTCTTGAACTTCTGATCTCAAGTGATCCTCACTCCTCAGCCTCCCAAATTGC GTCAGCCAGGCTTTTCTTGAACTTCTGATCTC___TGATCCTCACTCCTCAGCCTCCCAAATTGC ACTT A ARPIN,ARPIN-AP3S2 Ensembl:ENSG00000242498,Ensembl:ENSG00000250021 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1461713852 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_466701,Human_RBP_ID_4339399,Human_RBP_ID_12634285 RMVar_hsa_circ_347469,RMVar_hsa_circ_56287 48423 RMVar_ID_48423 Human_SNP_ID_587153486 A-to-I Human chr15 - 89897267 89897265 89897268 TCAGCCAGGCTTTTCTTGAACTTCTGATCTCAAGTGATCCTCACTCCTCAGCCTCCCAAATTGCT TCAGCCAGGCTTTTCTTGAACTTCTGATCTC___TGATCCTCACTCCTCAGCCTCCCAAATTGCT ACTT A ARPIN,ARPIN-AP3S2 Ensembl:ENSG00000242498,Ensembl:ENSG00000250021 Protein coding,Protein coding 3'UTR,intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs1461713852 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_4339399,Human_RBP_ID_12634285 RMVar_hsa_circ_347469,RMVar_hsa_circ_56287 48424 RMVar_ID_48424 Human_SNP_ID_587153491 A-to-I Human chr15 - 89897302 89897302 89897302 TTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTCAGCCAGGCTTTTCTTGAACTTCTGATCT TTTTGTATTTTTAGTAGAGACGGGGTTTCACCTTGTCAGCCAGGCTTTTCTTGAACTTCTGATCT T A ARPIN,ARPIN-AP3S2 Ensembl:ENSG00000242498,Ensembl:ENSG00000250021 Protein coding,Protein coding 3'UTR,intron GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs1013262416 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_347469,RMVar_hsa_circ_56287 48425 RMVar_ID_48425 Human_SNP_ID_587153492 A-to-I Human chr15 - 89897302 89897302 89897302 TTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTCAGCCAGGCTTTTCTTGAACTTCTGATCT TTTTGTATTTTTAGTAGAGACGGGGTTTCACCGTGTCAGCCAGGCTTTTCTTGAACTTCTGATCT T C ARPIN,ARPIN-AP3S2 Ensembl:ENSG00000242498,Ensembl:ENSG00000250021 Protein coding,Protein coding 3'UTR,intron GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs1013262416 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_347469,RMVar_hsa_circ_56287 48426 RMVar_ID_48426 Human_SNP_ID_587153635 A-to-I Human chr15 - 89897864 89897864 89897864 GAACTCCTGACCTCAGGTGATCCACCCTCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAG GAACTCCTGACCTCAGGTGATCCACCCTCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAG T C ARPIN,ARPIN-AP3S2 Ensembl:ENSG00000242498,Ensembl:ENSG00000250021 Protein coding,Protein coding 3'UTR,intron GSE123020:GSM3490829,GSM3490830,GSM3490831 esophageal squamous carcinoma cells,EC109 cell line - 32596459 RNA-Seq:(High) rs924268882 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_347469,RMVar_hsa_circ_56287 48427 RMVar_ID_48427 Human_SNP_ID_587153654 A-to-I Human chr15 - 89897936 89897936 89897936 GCGCCACCACGACTAGCTAATTTTGTACTTTTAGTAGAGATGCGATTTCACCATGTTGGCTAGGC GCGCCACCACGACTAGCTAATTTTGTACTTTTGGTAGAGATGCGATTTCACCATGTTGGCTAGGC T C ARPIN,ARPIN-AP3S2 Ensembl:ENSG00000242498,Ensembl:ENSG00000250021 Protein coding,Protein coding 3'UTR,intron GSE100210;GSE112787;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831 HepG2 cell line;293 Flip-In T-REx cells,empty vector;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line - 29129909,29967493,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs1318402563 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12634291 RMVar_hsa_circ_347469,RMVar_hsa_circ_56287 48428 RMVar_ID_48428 Human_SNP_ID_587153688 A-to-I Human chr15 - 89898074 89898074 89898074 AATTTCGCTCTTGTTGCCCAGGCTGGAGTGCAATGGCTCAATCTCGGCTCACTGCAACCTCCACC AATTTCGCTCTTGTTGCCCAGGCTGGAGTGCAGTGGCTCAATCTCGGCTCACTGCAACCTCCACC T C ARPIN,ARPIN-AP3S2 Ensembl:ENSG00000242498,Ensembl:ENSG00000250021 Protein coding,Protein coding 3'UTR,intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs541557338 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_347469,RMVar_hsa_circ_56287 48429 RMVar_ID_48429 Human_SNP_ID_587153967 A-to-I Human chr15 - 89899180 89899180 89899180 CCTTGGGAGGCTGAGGCATGAGAATTTCTTGAACCCGGGAGGTGGAGGTTGCAGTGAGCTGAGAT CCTTGGGAGGCTGAGGCATGAGAATTTCTTGAGCCCGGGAGGTGGAGGTTGCAGTGAGCTGAGAT T C ARPIN,ARPIN-AP3S2 Ensembl:ENSG00000242498,Ensembl:ENSG00000250021 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1138082 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_347469,RMVar_hsa_circ_56287 48430 RMVar_ID_48430 Human_SNP_ID_587153968 A-to-I Human chr15 - 89899181 89899181 89899181 GCCTTGGGAGGCTGAGGCATGAGAATTTCTTGAACCCGGGAGGTGGAGGTTGCAGTGAGCTGAGA GCCTTGGGAGGCTGAGGCATGAGAATTTCTTGGACCCGGGAGGTGGAGGTTGCAGTGAGCTGAGA T C ARPIN,ARPIN-AP3S2 Ensembl:ENSG00000242498,Ensembl:ENSG00000250021 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1138077 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_347469,RMVar_hsa_circ_56287 48431 RMVar_ID_48431 Human_SNP_ID_587153977 A-to-I Human chr15 - 89899240 89899240 89899240 TCTCTACCAAAAAATACAAAAATTACCCGGACATGGTGGCACATGCCTGTAGTTCCAGCGCCTTG TCTCTACCAAAAAATACAAAAATTACCCGGACGTGGTGGCACATGCCTGTAGTTCCAGCGCCTTG T C ARPIN,ARPIN-AP3S2 Ensembl:ENSG00000242498,Ensembl:ENSG00000250021 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1138070 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_347469,RMVar_hsa_circ_56287 48432 RMVar_ID_48432 Human_SNP_ID_587153983 A-to-I Human chr15 - 89899260 89899250 89899260 ATCAACACAGTGAAACCCCGTCTCTACCAAAAAATACAAAAATTACCCGGACATGGTGGCACATG ATCAACACAGTGAAACCCCGTCTCTACCAAAA__________TTACCCGGACATGGTGGCACATG ATTTTTGTATT A ARPIN,ARPIN-AP3S2 Ensembl:ENSG00000242498,Ensembl:ENSG00000250021 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs930692331 Functional Loss DEL dbSNP153 33..42 33 - - - RMVar_hsa_circ_347469,RMVar_hsa_circ_56287 48433 RMVar_ID_48433 Human_SNP_ID_587153986 A-to-I Human chr15 - 89899260 89899260 89899260 ATCAACACAGTGAAACCCCGTCTCTACCAAAAAATACAAAAATTACCCGGACATGGTGGCACATG ATCAACACAGTGAAACCCCGTCTCTACCAAAAGATACAAAAATTACCCGGACATGGTGGCACATG T C ARPIN,ARPIN-AP3S2 Ensembl:ENSG00000242498,Ensembl:ENSG00000250021 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs3180007 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_347469,RMVar_hsa_circ_56287 48434 RMVar_ID_48434 Human_SNP_ID_587154210 A-to-I Human chr15 - 89900235 89900235 89900235 CTGCTTCCTTGCCCTTCAGAAAGGTCTTGGAAACAGGGGCCAGAGGATGTGGTAGCCACTTCACT CTGCTTCCTTGCCCTTCAGAAAGGTCTTGGAAGCAGGGGCCAGAGGATGTGGTAGCCACTTCACT T C ARPIN,ARPIN-AP3S2 Ensembl:ENSG00000242498,Ensembl:ENSG00000250021 Protein coding,Protein coding 3'UTR,intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1052574506 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1002585,Human_RBP_ID_9057684,Human_RBP_ID_17251575,Human_RBP_ID_17869046 RMVar_hsa_circ_347469,RMVar_hsa_circ_56287 48435 RMVar_ID_48435 Human_SNP_ID_587154211 A-to-I Human chr15 - 89900235 89900235 89900235 CTGCTTCCTTGCCCTTCAGAAAGGTCTTGGAAACAGGGGCCAGAGGATGTGGTAGCCACTTCACT CTGCTTCCTTGCCCTTCAGAAAGGTCTTGGAACCAGGGGCCAGAGGATGTGGTAGCCACTTCACT T G ARPIN,ARPIN-AP3S2 Ensembl:ENSG00000242498,Ensembl:ENSG00000250021 Protein coding,Protein coding 3'UTR,intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1052574506 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1002585,Human_RBP_ID_9057684,Human_RBP_ID_17251575,Human_RBP_ID_17869046 RMVar_hsa_circ_347469,RMVar_hsa_circ_56287 48436 RMVar_ID_48436 Human_SNP_ID_587154693 A-to-I Human chr15 - 89902246 89902246 89902246 GCGCCACCATGCCTGGCTAATTTTGTATTTTTAGTAGAGACGAGGTTTCTCCATGTTGGGCTGGT GCGCCACCATGCCTGGCTAATTTTGTATTTTTTGTAGAGACGAGGTTTCTCCATGTTGGGCTGGT T A ARPIN,ARPIN-AP3S2 Ensembl:ENSG00000242498,Ensembl:ENSG00000250021 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1269580198 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_347469,RMVar_hsa_circ_56287 48437 RMVar_ID_48437 Human_SNP_ID_182906000 A-to-I Human chr4 - 47680788 47680784 47680788 ATGATCACACCACTGCACTCCAGCCTGGGAGAAAGAGAGAGACCTTGTCTCAAAAAAAAGATAAT ATGATCACACCACTGCACTCCAGCCTGGGAGA____GAGAGACCTTGTCTCAAAAAAAAGATAAT CTCTT C CORIN Ensembl:ENSG00000145244 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1159291390 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_49984,RMVar_hsa_circ_28453,RMVar_hsa_circ_374073,RMVar_hsa_circ_269431,RMVar_hsa_circ_120944,RMVar_hsa_circ_225854,RMVar_hsa_circ_225855,RMVar_hsa_circ_356315,RMVar_hsa_circ_338084,RMVar_hsa_circ_56170,RMVar_hsa_circ_376488 48438 RMVar_ID_48438 Human_SNP_ID_182906000 A-to-I Human chr4 - 47680787 47680784 47680788 TGATCACACCACTGCACTCCAGCCTGGGAGAAAGAGAGAGACCTTGTCTCAAAAAAAAGATAATC TGATCACACCACTGCACTCCAGCCTGGGAGA____GAGAGACCTTGTCTCAAAAAAAAGATAATC CTCTT C CORIN Ensembl:ENSG00000145244 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1159291390 Functional Loss DEL dbSNP153 32..35 33 - - - RMVar_hsa_circ_49984,RMVar_hsa_circ_28453,RMVar_hsa_circ_374073,RMVar_hsa_circ_269431,RMVar_hsa_circ_120944,RMVar_hsa_circ_225854,RMVar_hsa_circ_225855,RMVar_hsa_circ_356315,RMVar_hsa_circ_338084,RMVar_hsa_circ_56170,RMVar_hsa_circ_376488 48439 RMVar_ID_48439 Human_SNP_ID_182906002 A-to-I Human chr4 - 47680788 47680788 47680788 ATGATCACACCACTGCACTCCAGCCTGGGAGAAAGAGAGAGACCTTGTCTCAAAAAAAAGATAAT ATGATCACACCACTGCACTCCAGCCTGGGAGAGAGAGAGAGACCTTGTCTCAAAAAAAAGATAAT T C CORIN Ensembl:ENSG00000145244 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1423040033 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49984,RMVar_hsa_circ_28453,RMVar_hsa_circ_374073,RMVar_hsa_circ_269431,RMVar_hsa_circ_120944,RMVar_hsa_circ_225854,RMVar_hsa_circ_225855,RMVar_hsa_circ_356315,RMVar_hsa_circ_338084,RMVar_hsa_circ_56170,RMVar_hsa_circ_376488 48440 RMVar_ID_48440 Human_SNP_ID_182946697 A-to-I Human chr4 - 47860945 47860945 47860945 GGGAGGCTGAGGCAGGAGAATCACTTGAACCCAGGAGGCGGAAGTTGCAGTGAGCCAAGATGGCG GGGAGGCTGAGGCAGGAGAATCACTTGAACCCCGGAGGCGGAAGTTGCAGTGAGCCAAGATGGCG T G NFXL1 Ensembl:ENSG00000170448 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1278106893 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119877,RMVar_hsa_circ_225862,RMVar_hsa_circ_277607,RMVar_hsa_circ_346119,RMVar_hsa_circ_275290,RMVar_hsa_circ_287145,RMVar_hsa_circ_324706,RMVar_hsa_circ_267796,RMVar_hsa_circ_225864,RMVar_hsa_circ_225866,RMVar_hsa_circ_36756,RMVar_hsa_circ_225865,RMVar_hsa_circ_225863 48441 RMVar_ID_48441 Human_SNP_ID_182956378 A-to-I Human chr4 - 47902974 47902974 47902974 ATTTTTTGTATTTTTAGTAGACACAGGGTTTCACCATGTCTGCCAGGCTGGTCTTGAACTCCTGA ATTTTTTGTATTTTTAGTAGACACAGGGTTTCGCCATGTCTGCCAGGCTGGTCTTGAACTCCTGA T C NFXL1 Ensembl:ENSG00000170448 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893697607 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_275290,RMVar_hsa_circ_225866,RMVar_hsa_circ_346834,RMVar_hsa_circ_265364,RMVar_hsa_circ_318793,RMVar_hsa_circ_225868,RMVar_hsa_circ_352556,RMVar_hsa_circ_315326,RMVar_hsa_circ_360957,RMVar_hsa_circ_225869,RMVar_hsa_circ_354077,RMVar_hsa_circ_328420,RMVar_hsa_circ_225877,RMVar_hsa_circ_76154,RMVar_hsa_circ_93523,RMVar_hsa_circ_225876,RMVar_hsa_circ_225887,RMVar_hsa_circ_83459,RMVar_hsa_circ_374226,RMVar_hsa_circ_225891,RMVar_hsa_circ_225888,RMVar_hsa_circ_69457,RMVar_hsa_circ_225889,RMVar_hsa_circ_299372,RMVar_hsa_circ_299417,RMVar_hsa_circ_97995,RMVar_hsa_circ_43941,RMVar_hsa_circ_225892,RMVar_hsa_circ_225890,RMVar_hsa_circ_369831,RMVar_hsa_circ_357931 48442 RMVar_ID_48442 Human_SNP_ID_183001685 A-to-I Human chr4 - 48096704 48096704 48096704 GCCAACACGGTGAAACCTTGTCTCCACAAAAAATACAAAAATTAGCCAGGCATGGTGGCATGTGC GCCAACACGGTGAAACCTTGTCTCCACAAAAAGTACAAAAATTAGCCAGGCATGGTGGCATGTGC T C TXK Ensembl:ENSG00000074966 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1259707250 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3742,RMVar_hsa_circ_53343,RMVar_hsa_circ_62737,RMVar_hsa_circ_71237,RMVar_hsa_circ_360652,RMVar_hsa_circ_65811,RMVar_hsa_circ_53473,RMVar_hsa_circ_116485,RMVar_hsa_circ_358015,RMVar_hsa_circ_225895 48443 RMVar_ID_48443 Human_SNP_ID_183010329 A-to-I Human chr4 - 48132506 48132506 48132506 ATGTGTATATTTGTATACATATAAAGCTGCCAACTGTGATCCACAAATGCTGGACGAAATCAGAA ATGTGTATATTTGTATACATATAAAGCTGCCAGCTGTGATCCACAAATGCTGGACGAAATCAGAA T C TXK Ensembl:ENSG00000074966 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1160660740 Functional Loss SNV dbSNP153 33..33 33 - - - 48444 RMVar_ID_48444 Human_SNP_ID_183010332 A-to-I Human chr4 - 48132516 48132516 48132516 GAGTGTGTGTATGTGTATATTTGTATACATATAAAGCTGCCAACTGTGATCCACAAATGCTGGAC GAGTGTGTGTATGTGTATATTTGTATACATATGAAGCTGCCAACTGTGATCCACAAATGCTGGAC T C TXK Ensembl:ENSG00000074966 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1180119587 Functional Loss SNV dbSNP153 33..33 33 - - - 48445 RMVar_ID_48445 Human_SNP_ID_183010648 A-to-I Human chr4 - 48133781 48133781 48133781 GTTCTGGATTTGCTCCAGCAGTGGTGGATCACAGTGGGCAACTTTATATATATATAAATACACAC GTTCTGGATTTGCTCCAGCAGTGGTGGATCACGGTGGGCAACTTTATATATATATAAATACACAC T C TXK Ensembl:ENSG00000074966 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1398484372 Functional Loss SNV dbSNP153 33..33 33 - - - 48446 RMVar_ID_48446 Human_SNP_ID_183010649 A-to-I Human chr4 - 48133781 48133781 48133781 GTTCTGGATTTGCTCCAGCAGTGGTGGATCACAGTGGGCAACTTTATATATATATAAATACACAC GTTCTGGATTTGCTCCAGCAGTGGTGGATCACCGTGGGCAACTTTATATATATATAAATACACAC T G TXK Ensembl:ENSG00000074966 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1398484372 Functional Loss SNV dbSNP153 33..33 33 - - - 48447 RMVar_ID_48447 Human_SNP_ID_183012542 A-to-I Human chr4 - 48141821 48141821 48141821 ATAATTAGCTGGCTGTGGTGGTGGGTGCCTGTAATCCCAGCTACTCTGGAGGCTGGGGCAGAAGA ATAATTAGCTGGCTGTGGTGGTGGGTGCCTGTGATCCCAGCTACTCTGGAGGCTGGGGCAGAAGA T C TEC Ensembl:ENSG00000135605 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1486976418 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118326,RMVar_hsa_circ_225898,RMVar_hsa_circ_96499,RMVar_hsa_circ_225897 48448 RMVar_ID_48448 Human_SNP_ID_183012546 A-to-I Human chr4 - 48141847 48141847 48141847 CAAGACCAGCCTGGCCAACAAATACAATAATTAGCTGGCTGTGGTGGTGGGTGCCTGTAATCCCA CAAGACCAGCCTGGCCAACAAATACAATAATTGGCTGGCTGTGGTGGTGGGTGCCTGTAATCCCA T C TEC Ensembl:ENSG00000135605 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1485319609 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118326,RMVar_hsa_circ_225898,RMVar_hsa_circ_96499,RMVar_hsa_circ_225897 48449 RMVar_ID_48449 Human_SNP_ID_183012563 A-to-I Human chr4 - 48141929 48141929 48141929 ATGACAGTTGGCCGGTGAGGTTGCTCGTGACTATAATCCTAACAATGGGGGAGGCCGAGGCAGAT ATGACAGTTGGCCGGTGAGGTTGCTCGTGACTGTAATCCTAACAATGGGGGAGGCCGAGGCAGAT T C TEC Ensembl:ENSG00000135605 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1413859020 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118326,RMVar_hsa_circ_225898,RMVar_hsa_circ_96499,RMVar_hsa_circ_225897 48450 RMVar_ID_48450 Human_SNP_ID_183012654 A-to-I Human chr4 - 48142352 48142352 48142352 TCTCCTGCCTCCAGTCCTAGGTAGCTGGTACTACAGTTGTGTGCCACCACACTTGGCTAATTTTT TCTCCTGCCTCCAGTCCTAGGTAGCTGGTACTGCAGTTGTGTGCCACCACACTTGGCTAATTTTT T C TEC Ensembl:ENSG00000135605 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs904684868 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118326,RMVar_hsa_circ_225898,RMVar_hsa_circ_96499,RMVar_hsa_circ_225897 48451 RMVar_ID_48451 Human_SNP_ID_183013051 A-to-I Human chr4 - 48143990 48143990 48143990 GAACTCTTGAGCTTAAGCAATCTGCCTGCCTCAGCCTCCCAAGTGCTAGGATTACAGGTGTGAGC GAACTCTTGAGCTTAAGCAATCTGCCTGCCTCTGCCTCCCAAGTGCTAGGATTACAGGTGTGAGC T A TEC Ensembl:ENSG00000135605 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs577527295 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118326,RMVar_hsa_circ_225898,RMVar_hsa_circ_96499,RMVar_hsa_circ_225897 48452 RMVar_ID_48452 Human_SNP_ID_183013052 A-to-I Human chr4 - 48143990 48143990 48143990 GAACTCTTGAGCTTAAGCAATCTGCCTGCCTCAGCCTCCCAAGTGCTAGGATTACAGGTGTGAGC GAACTCTTGAGCTTAAGCAATCTGCCTGCCTCGGCCTCCCAAGTGCTAGGATTACAGGTGTGAGC T C TEC Ensembl:ENSG00000135605 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs577527295 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118326,RMVar_hsa_circ_225898,RMVar_hsa_circ_96499,RMVar_hsa_circ_225897 48453 RMVar_ID_48453 Human_SNP_ID_183014729 A-to-I Human chr4 - 48151575 48151575 48151575 GGCTGAGGCAGGAGAACTGCTTGAACCCAGGAAGTGGAGATTGCAGTGAGCTGAGATCGCACCAC GGCTGAGGCAGGAGAACTGCTTGAACCCAGGAGGTGGAGATTGCAGTGAGCTGAGATCGCACCAC T C TEC Ensembl:ENSG00000135605 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs970790137 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118326,RMVar_hsa_circ_225898,RMVar_hsa_circ_108206,RMVar_hsa_circ_225899 48454 RMVar_ID_48454 Human_SNP_ID_183014740 A-to-I Human chr4 - 48151615 48151615 48151615 GGACATGGTGTTGCACACCTGTAATTCCAGCTACTCGGGAGGCTGAGGCAGGAGAACTGCTTGAA GGACATGGTGTTGCACACCTGTAATTCCAGCTGCTCGGGAGGCTGAGGCAGGAGAACTGCTTGAA T C TEC Ensembl:ENSG00000135605 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1560377148 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118326,RMVar_hsa_circ_225898,RMVar_hsa_circ_108206,RMVar_hsa_circ_225899 48455 RMVar_ID_48455 Human_SNP_ID_183016688 A-to-I Human chr4 - 48160546 48160546 48160546 ATTTTTGTATTTTTAGTAGAGACAGGGTTTCAATATGTTGGCCAGGCTGGTCTCAAACTCTTGAC ATTTTTGTATTTTTAGTAGAGACAGGGTTTCAGTATGTTGGCCAGGCTGGTCTCAAACTCTTGAC T C TEC Ensembl:ENSG00000135605 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1261902055 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_118326,RMVar_hsa_circ_55064,RMVar_hsa_circ_225898,RMVar_hsa_circ_108206,RMVar_hsa_circ_225899 48456 RMVar_ID_48456 Human_SNP_ID_183135453 A-to-I Human chr4 - 48677683 48677683 48677683 TTTTCGGGCTGACGCGGTGGCTCACGCTTGTAATCCCAGCAATTTGGGAGGCCAAGGCAGGCGGA TTTTCGGGCTGACGCGGTGGCTCACGCTTGTAGTCCCAGCAATTTGGGAGGCCAAGGCAGGCGGA T C FRYL Ensembl:ENSG00000075539 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1328903013 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123036,RMVar_hsa_circ_225937,RMVar_hsa_circ_78704,RMVar_hsa_circ_225955,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_315209,RMVar_hsa_circ_225971,RMVar_hsa_circ_225972 48457 RMVar_ID_48457 Human_SNP_ID_183135615 A-to-I Human chr4 - 48678426 48678426 48678426 TGGCTCACTGCAACCTCCGCCTCCCTTGTTCAAGCGATTCTCCTGCCTCAGTCCCCCTGAGTAGC TGGCTCACTGCAACCTCCGCCTCCCTTGTTCAGGCGATTCTCCTGCCTCAGTCCCCCTGAGTAGC T C FRYL Ensembl:ENSG00000075539 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1258349902 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123036,RMVar_hsa_circ_225937,RMVar_hsa_circ_78704,RMVar_hsa_circ_225955,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_315209,RMVar_hsa_circ_225971,RMVar_hsa_circ_225972 48458 RMVar_ID_48458 Human_SNP_ID_183155539 A-to-I Human chr4 - 48764358 48764358 48764358 CCCGGCTAACCTTTTGATTTTTTTGTAGAGACAAGGTCTCACTTTGTTGCACCGGGCTGGTCTTG CCCGGCTAACCTTTTGATTTTTTTGTAGAGACGAGGTCTCACTTTGTTGCACCGGGCTGGTCTTG T C FRYL Ensembl:ENSG00000075539 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1273955013 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123036,RMVar_hsa_circ_225937,RMVar_hsa_circ_100943,RMVar_hsa_circ_225978,RMVar_hsa_circ_103285,RMVar_hsa_circ_225980 48459 RMVar_ID_48459 Human_SNP_ID_183157693 A-to-I Human chr4 - 48773757 48773757 48773757 ATGTGCCACCACACCCAGCTATTTTTTGTAGAAAGAGGATCTTGCCATGTTGCCTAGGCTGATCT ATGTGCCACCACACCCAGCTATTTTTTGTAGACAGAGGATCTTGCCATGTTGCCTAGGCTGATCT T G FRYL Ensembl:ENSG00000075539 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs962934990 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123036,RMVar_hsa_circ_225937,RMVar_hsa_circ_100943,RMVar_hsa_circ_225978,RMVar_hsa_circ_103285,RMVar_hsa_circ_225980 48460 RMVar_ID_48460 Human_SNP_ID_183157890 A-to-I Human chr4 - 48774656 48774656 48774656 CTGTAGTCCCAGGTACTCTGGAGTCTGAGGCAAGAGAATCGCTTGAACCCAGGAGGCGGAAGTTG CTGTAGTCCCAGGTACTCTGGAGTCTGAGGCAGGAGAATCGCTTGAACCCAGGAGGCGGAAGTTG T C FRYL Ensembl:ENSG00000075539 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1161508504 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123036,RMVar_hsa_circ_225937,RMVar_hsa_circ_100943,RMVar_hsa_circ_225978,RMVar_hsa_circ_103285,RMVar_hsa_circ_225980 48461 RMVar_ID_48461 Human_SNP_ID_183172228 A-to-I Human chr4 + 48834352 48834352 48834352 TGCAACCATGCCCAGCAAATTTTTCTATTTCTAGTAGAAGCGGGATTTCACCATGTTGGCCAGGC TGCAACCATGCCCAGCAAATTTTTCTATTTCTGGTAGAAGCGGGATTTCACCATGTTGGCCAGGC A G OCIAD1 Ensembl:ENSG00000109180 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1000423242 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7315235 RMVar_hsa_circ_51256,RMVar_hsa_circ_225983,RMVar_hsa_circ_317615,RMVar_hsa_circ_344933,RMVar_hsa_circ_328438,RMVar_hsa_circ_115340,RMVar_hsa_circ_269179,RMVar_hsa_circ_307251,RMVar_hsa_circ_330239,RMVar_hsa_circ_225982,RMVar_hsa_circ_321902,RMVar_hsa_circ_281679,RMVar_hsa_circ_225985,RMVar_hsa_circ_51182 48462 RMVar_ID_48462 Human_SNP_ID_183172268 A-to-I Human chr4 + 48834512 48834512 48834512 AAAAAGGCAACTTGGCACGGTGCCTCATGGCTATAATTGCAGCACTTTGGGAGGCTGAGGCAGGA AAAAAGGCAACTTGGCACGGTGCCTCATGGCTGTAATTGCAGCACTTTGGGAGGCTGAGGCAGGA A G OCIAD1 Ensembl:ENSG00000109180 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs540468807 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51256,RMVar_hsa_circ_225983,RMVar_hsa_circ_317615,RMVar_hsa_circ_344933,RMVar_hsa_circ_328438,RMVar_hsa_circ_115340,RMVar_hsa_circ_269179,RMVar_hsa_circ_307251,RMVar_hsa_circ_330239,RMVar_hsa_circ_225982,RMVar_hsa_circ_321902,RMVar_hsa_circ_281679,RMVar_hsa_circ_225985,RMVar_hsa_circ_51182 48463 RMVar_ID_48463 Human_SNP_ID_183172404 A-to-I Human chr4 + 48835117 48835117 48835117 CACCATGCCCGGCTAATTTTTGTATTTTCAGTAGAGACTGGGTTTCACTATGTTGGCCAGGCTGA CACCATGCCCGGCTAATTTTTGTATTTTCAGTGGAGACTGGGTTTCACTATGTTGGCCAGGCTGA A G OCIAD1 Ensembl:ENSG00000109180 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs977819228 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51256,RMVar_hsa_circ_225983,RMVar_hsa_circ_317615,RMVar_hsa_circ_344933,RMVar_hsa_circ_328438,RMVar_hsa_circ_115340,RMVar_hsa_circ_269179,RMVar_hsa_circ_307251,RMVar_hsa_circ_330239,RMVar_hsa_circ_225982,RMVar_hsa_circ_321902,RMVar_hsa_circ_281679,RMVar_hsa_circ_225985,RMVar_hsa_circ_51182 48464 RMVar_ID_48464 Human_SNP_ID_183172521 A-to-I Human chr4 + 48835711 48835711 48835711 CCTGCCTTGGCCTCCCCAAATGGTGGAATTTCAAGCATGAGCCACTGAACCTGGCCCCAGCACAT CCTGCCTTGGCCTCCCCAAATGGTGGAATTTCTAGCATGAGCCACTGAACCTGGCCCCAGCACAT A T OCIAD1 Ensembl:ENSG00000109180 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs999147426 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15165791 RMVar_hsa_circ_51256,RMVar_hsa_circ_225983,RMVar_hsa_circ_317615,RMVar_hsa_circ_344933,RMVar_hsa_circ_328438,RMVar_hsa_circ_115340,RMVar_hsa_circ_269179,RMVar_hsa_circ_307251,RMVar_hsa_circ_330239,RMVar_hsa_circ_225982,RMVar_hsa_circ_321902,RMVar_hsa_circ_281679,RMVar_hsa_circ_225985,RMVar_hsa_circ_51182 48465 RMVar_ID_48465 Human_SNP_ID_183172836 A-to-I Human chr4 + 48837101 48837101 48837101 TCATACCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCGCCTGCCACCATACCTG TCATACCATTCTCCTGCCTCAGCCTCCCGAGTGGCTGGGATTACAGGCGCCTGCCACCATACCTG A G OCIAD1 Ensembl:ENSG00000109180 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1158168381 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51256,RMVar_hsa_circ_225983,RMVar_hsa_circ_317615,RMVar_hsa_circ_344933,RMVar_hsa_circ_328438,RMVar_hsa_circ_115340,RMVar_hsa_circ_269179,RMVar_hsa_circ_307251,RMVar_hsa_circ_330239,RMVar_hsa_circ_225982,RMVar_hsa_circ_321902,RMVar_hsa_circ_281679,RMVar_hsa_circ_225985,RMVar_hsa_circ_51182 48466 RMVar_ID_48466 Human_SNP_ID_183173114 A-to-I Human chr4 + 48838153 48838153 48838153 CAGCCTGACCTATATGGTGAAACCCCGTCTCTACTAAGAATACAAAAATTAGCTGAGCATGGTGG CAGCCTGACCTATATGGTGAAACCCCGTCTCTGCTAAGAATACAAAAATTAGCTGAGCATGGTGG A G OCIAD1 Ensembl:ENSG00000109180 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1560422648 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_51256,RMVar_hsa_circ_225983,RMVar_hsa_circ_317615,RMVar_hsa_circ_344933,RMVar_hsa_circ_328438,RMVar_hsa_circ_115340,RMVar_hsa_circ_269179,RMVar_hsa_circ_307251,RMVar_hsa_circ_330239,RMVar_hsa_circ_225982,RMVar_hsa_circ_321902,RMVar_hsa_circ_281679,RMVar_hsa_circ_225985,RMVar_hsa_circ_51182 48467 RMVar_ID_48467 Human_SNP_ID_183176567 A-to-I Human chr4 + 48853064 48853064 48853064 ACCACGCTCGGCTAATTTTTTGTATTTTTAGTAGAGATGGGGTTTCACTGTGTTGGCCAGGATGG ACCACGCTCGGCTAATTTTTTGTATTTTTAGTGGAGATGGGGTTTCACTGTGTTGGCCAGGATGG A G OCIAD1 Ensembl:ENSG00000109180 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1029393337 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269179,RMVar_hsa_circ_281679,RMVar_hsa_circ_225985,RMVar_hsa_circ_225986,RMVar_hsa_circ_296033,RMVar_hsa_circ_225987,RMVar_hsa_circ_324043,RMVar_hsa_circ_225989,RMVar_hsa_circ_286205,RMVar_hsa_circ_225990 48468 RMVar_ID_48468 Human_SNP_ID_183177037 A-to-I Human chr4 + 48855621 48855621 48855621 GGGTGGATCACCTGAGGTCAGAGTTCAAGACCAGCCTGACCAATATGGCGAAACCCTGTCTCTAC GGGTGGATCACCTGAGGTCAGAGTTCAAGACCCGCCTGACCAATATGGCGAAACCCTGTCTCTAC A C OCIAD1 Ensembl:ENSG00000109180 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459304885 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269179,RMVar_hsa_circ_281679,RMVar_hsa_circ_225985,RMVar_hsa_circ_225986,RMVar_hsa_circ_296033,RMVar_hsa_circ_225987,RMVar_hsa_circ_324043,RMVar_hsa_circ_225989,RMVar_hsa_circ_286205,RMVar_hsa_circ_225990 48469 RMVar_ID_48469 Human_SNP_ID_183177591 A-to-I Human chr4 + 48857904 48857904 48857904 GGCCAGGTGTGGTGTCTCATGCCTGAAATCCCAGCACTTTGGGAGACCAAGCTGGGTGTATCACT GGCCAGGTGTGGTGTCTCATGCCTGAAATCCCGGCACTTTGGGAGACCAAGCTGGGTGTATCACT A G OCIAD1 Ensembl:ENSG00000109180 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1413707786 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17574759 RMVar_hsa_circ_225990 48470 RMVar_ID_48470 Human_SNP_ID_183293861 A-to-I Human chr4 + 49154452 49154448 49154452 CCACTTGTGTTGATTCCATTCCATTCCATTCCATTCCATTCCATTCCATTCCATTCCATTCCATT CCACTTGTGTTGATTCCATTCCATTCCAT____TTCCATTCCATTCCATTCCATTCCATTCCATT TTCCA T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335316867 Functional Loss DEL dbSNP153 30..33 33 - - - 48471 RMVar_ID_48471 Human_SNP_ID_183293862 A-to-I Human chr4 + 49154452 49154452 49154452 CCACTTGTGTTGATTCCATTCCATTCCATTCCATTCCATTCCATTCCATTCCATTCCATTCCATT CCACTTGTGTTGATTCCATTCCATTCCATTCCTTTCCATTCCATTCCATTCCATTCCATTCCATT A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs889951956 Functional Loss SNV dbSNP153 33..33 33 - - - 48472 RMVar_ID_48472 Human_SNP_ID_183488213 A-to-I Human chr4 + 49650228 49650223 49650228 TGGAATCAACCCGAGTGAAATGGAATGGAAAGAAATGGAATGGAATCAACAGGAGTGCAATGGAA TGGAATCAACCCGAGTGAAATGGAATGG_____AATGGAATGGAATCAACAGGAGTGCAATGGAA GAAAGA G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs368698272 Functional Loss DEL dbSNP153 29..33 33 - - - 48473 RMVar_ID_48473 Human_SNP_ID_183488218 A-to-I Human chr4 + 49650228 49650228 49650228 TGGAATCAACCCGAGTGAAATGGAATGGAAAGAAATGGAATGGAATCAACAGGAGTGCAATGGAA TGGAATCAACCCGAGTGAAATGGAATGGAAAGCAATGGAATGGAATCAACAGGAGTGCAATGGAA A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs10446987 Functional Loss SNV dbSNP153 33..33 33 - - - 48474 RMVar_ID_48474 Human_SNP_ID_183488219 A-to-I Human chr4 + 49650228 49650228 49650228 TGGAATCAACCCGAGTGAAATGGAATGGAAAGAAATGGAATGGAATCAACAGGAGTGCAATGGAA TGGAATCAACCCGAGTGAAATGGAATGGAAAGGAATGGAATGGAATCAACAGGAGTGCAATGGAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs10446987 Functional Loss SNV dbSNP153 33..33 33 - - - 48475 RMVar_ID_48475 Human_SNP_ID_183488220 A-to-I Human chr4 + 49650228 49650228 49650228 TGGAATCAACCCGAGTGAAATGGAATGGAAAGAAATGGAATGGAATCAACAGGAGTGCAATGGAA TGGAATCAACCCGAGTGAAATGGAATGGAAAGTAATGGAATGGAATCAACAGGAGTGCAATGGAA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs10446987 Functional Loss SNV dbSNP153 33..33 33 - - - 48476 RMVar_ID_48476 Human_SNP_ID_183488489 A-to-I Human chr4 + 49650524 49650524 49650524 GAAATGGAATGGAATGGAACGGAATCAACCCGAATGGAATGGAATGGAATGGAATGGAAAGCAAT GAAATGGAATGGAATGGAACGGAATCAACCCGGATGGAATGGAATGGAATGGAATGGAAAGCAAT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs554015224 Functional Loss SNV dbSNP153 33..33 33 - - - 48477 RMVar_ID_48477 Human_SNP_ID_183797797 A-to-I Human chr4 + 51887162 51887162 51887162 CTCGCACTGTCGCCAGGCTGGAGTGCAATGGTATGATGTCGGCTCACTGCAACCTCTGCCTCCCG CTCGCACTGTCGCCAGGCTGGAGTGCAATGGTGTGATGTCGGCTCACTGCAACCTCTGCCTCCCG A G DCUN1D4 Ensembl:ENSG00000109184 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs947681455 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_560575,Human_Splice_Rec_560630,Human_Splice_Rec_560701,Human_Splice_Rec_560724,Human_Splice_Rec_560725 RMVar_hsa_circ_336190,RMVar_hsa_circ_305553,RMVar_hsa_circ_25022,RMVar_hsa_circ_226003,RMVar_hsa_circ_225999,RMVar_hsa_circ_225993,RMVar_hsa_circ_225998,RMVar_hsa_circ_365017,RMVar_hsa_circ_371026,RMVar_hsa_circ_318039,RMVar_hsa_circ_274720,RMVar_hsa_circ_269841,RMVar_hsa_circ_54216,RMVar_hsa_circ_226005,RMVar_hsa_circ_226004,RMVar_hsa_circ_65576,RMVar_hsa_circ_226014,RMVar_hsa_circ_226001,RMVar_hsa_circ_226002,RMVar_hsa_circ_280780,RMVar_hsa_circ_226000,RMVar_hsa_circ_271734,RMVar_hsa_circ_226012,RMVar_hsa_circ_226013,RMVar_hsa_circ_311712 48478 RMVar_ID_48478 Human_SNP_ID_183798203 A-to-I Human chr4 + 51888644 51888644 51888644 AGGAGGTTGAGGCAGGAGAATCGCTTGAACCCAGGAGGTGGAGGTTGCAGTGAGCAGAGCCGACA AGGAGGTTGAGGCAGGAGAATCGCTTGAACCCGGGAGGTGGAGGTTGCAGTGAGCAGAGCCGACA A G DCUN1D4 Ensembl:ENSG00000109184 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893298364 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_336190,RMVar_hsa_circ_305553,RMVar_hsa_circ_25022,RMVar_hsa_circ_226003,RMVar_hsa_circ_225999,RMVar_hsa_circ_225993,RMVar_hsa_circ_225998,RMVar_hsa_circ_365017,RMVar_hsa_circ_318039,RMVar_hsa_circ_274720,RMVar_hsa_circ_269841,RMVar_hsa_circ_54216,RMVar_hsa_circ_226004,RMVar_hsa_circ_65576,RMVar_hsa_circ_226014,RMVar_hsa_circ_226001,RMVar_hsa_circ_226002,RMVar_hsa_circ_280780,RMVar_hsa_circ_226000,RMVar_hsa_circ_271734,RMVar_hsa_circ_226012,RMVar_hsa_circ_226013,RMVar_hsa_circ_311712 48479 RMVar_ID_48479 Human_SNP_ID_183839091 A-to-I Human chr4 - 52024647 52024647 52024647 AGTTTTTGTATTTTTAGTAGAGACGAGGTTTCACCGTGTTAGCCAGGATGGTCTCGATCTCCTGA AGTTTTTGTATTTTTAGTAGAGACGAGGTTTCGCCGTGTTAGCCAGGATGGTCTCGATCTCCTGA T C SGCB Ensembl:ENSG00000163069 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1273187201 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269679 48480 RMVar_ID_48480 Human_SNP_ID_183839093 A-to-I Human chr4 - 52024661 52024661 52024661 ACCACGTCCCGCTAAGTTTTTGTATTTTTAGTAGAGACGAGGTTTCACCGTGTTAGCCAGGATGG ACCACGTCCCGCTAAGTTTTTGTATTTTTAGTGGAGACGAGGTTTCACCGTGTTAGCCAGGATGG T C SGCB Ensembl:ENSG00000163069 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1307618422 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_269679 48481 RMVar_ID_48481 Human_SNP_ID_184029682 A-to-I Human chr4 + 52662346 52662346 52662346 GCTGATAGCTAGGACATGAACAGAATGCACCCAAGCACTTTGCTAAGGCAAAACATGCGTGACCT GCTGATAGCTAGGACATGAACAGAATGCACCCGAGCACTTTGCTAAGGCAAAACATGCGTGACCT A G USP46-AS1,USP46-AS1:2,USP46-AS1:3,USP46-AS1:4,USP46-AS1:5,USP46-AS1:6,USP46-AS1:7,USP46-AS1:8,USP46-AS1:9,USP46-AS1:10,USP46-AS1:11 RNACentral:URS0000D5D6A5,RNACentral:URS0000D597A4,RNACentral:URS00009C1D68,RNACentral:URS0000D5E3DD,RNACentral:URS0000D5C6C1,RNACentral:URS0000D5A550,RNACentral:URS00008B8402,RNACentral:URS00009BDDEB,RNACentral:URS0000D57F01,RNACentral:URS0000D58E33,RNACentral:URS0000D5C70E lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,intron,exon,exon,exon,exon,intron,intron,exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs894217491 Functional Loss SNV dbSNP153 33..33 33 - - - 48482 RMVar_ID_48482 Human_SNP_ID_184029695 A-to-I Human chr4 + 52662396 52662396 52662396 AAACATGCGTGACCTTTGCTCTAGTTCCCAATAATTTCCTTATTTCCATTCGAGACCTCAGAAGC AAACATGCGTGACCTTTGCTCTAGTTCCCAATGATTTCCTTATTTCCATTCGAGACCTCAGAAGC A G USP46-AS1,USP46-AS1:2,USP46-AS1:3,USP46-AS1:4,USP46-AS1:5,USP46-AS1:6,USP46-AS1:7,USP46-AS1:8,USP46-AS1:9,USP46-AS1:10,USP46-AS1:11 RNACentral:URS0000D5D6A5,RNACentral:URS0000D597A4,RNACentral:URS00009C1D68,RNACentral:URS0000D5E3DD,RNACentral:URS0000D5C6C1,RNACentral:URS0000D5A550,RNACentral:URS00008B8402,RNACentral:URS00009BDDEB,RNACentral:URS0000D57F01,RNACentral:URS0000D58E33,RNACentral:URS0000D5C70E lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,intron,intron,exon,intron,intron,exon,intron,intron,exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs887051283 Functional Loss SNV dbSNP153 33..33 33 - - - 48483 RMVar_ID_48483 Human_SNP_ID_184029713 A-to-I Human chr4 + 52662476 52662476 52662476 AAATGCTGATAGTGATGTGAACAGTGAAGTCCAGGCTGCTGAGGCCTCAGATGGAAATTAGGAAC AAATGCTGATAGTGATGTGAACAGTGAAGTCCGGGCTGCTGAGGCCTCAGATGGAAATTAGGAAC A G USP46-AS1,USP46-AS1:2,USP46-AS1:3,USP46-AS1:4,USP46-AS1:5,USP46-AS1:6,USP46-AS1:7,USP46-AS1:8,USP46-AS1:9,USP46-AS1:10,USP46-AS1:11 RNACentral:URS0000D5D6A5,RNACentral:URS0000D597A4,RNACentral:URS00009C1D68,RNACentral:URS0000D5E3DD,RNACentral:URS0000D5C6C1,RNACentral:URS0000D5A550,RNACentral:URS00008B8402,RNACentral:URS00009BDDEB,RNACentral:URS0000D57F01,RNACentral:URS0000D58E33,RNACentral:URS0000D5C70E lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,intron,intron,exon,intron,intron,exon,intron,intron,exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs551192593 Functional Loss SNV dbSNP153 33..33 33 - - - 48484 RMVar_ID_48484 Human_SNP_ID_184030111 A-to-I Human chr4 + 52664149 52664149 52664149 ACTCTCTATCTCTCTTGCTCCTGCTCTGCTATATGAGACACCTGTTCCCCGTTTGCCTTCCACCA ACTCTCTATCTCTCTTGCTCCTGCTCTGCTATGTGAGACACCTGTTCCCCGTTTGCCTTCCACCA A G USP46-AS1,USP46-AS1:2,USP46-AS1:3,USP46-AS1:4,USP46-AS1:5,USP46-AS1:6,USP46-AS1:7,USP46-AS1:8,USP46-AS1:9,USP46-AS1:10,USP46-AS1:11 RNACentral:URS0000D5D6A5,RNACentral:URS0000D597A4,RNACentral:URS00009C1D68,RNACentral:URS0000D5E3DD,RNACentral:URS0000D5C6C1,RNACentral:URS0000D5A550,RNACentral:URS00008B8402,RNACentral:URS00009BDDEB,RNACentral:URS0000D57F01,RNACentral:URS0000D58E33,RNACentral:URS0000D5C70E lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,exon,exon,exon,exon,exon,intron,exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1321312428 Functional Loss SNV dbSNP153 33..33 33 - - - 48485 RMVar_ID_48485 Human_SNP_ID_184030112 A-to-I Human chr4 + 52664149 52664149 52664149 ACTCTCTATCTCTCTTGCTCCTGCTCTGCTATATGAGACACCTGTTCCCCGTTTGCCTTCCACCA ACTCTCTATCTCTCTTGCTCCTGCTCTGCTATTTGAGACACCTGTTCCCCGTTTGCCTTCCACCA A T USP46-AS1,USP46-AS1:2,USP46-AS1:3,USP46-AS1:4,USP46-AS1:5,USP46-AS1:6,USP46-AS1:7,USP46-AS1:8,USP46-AS1:9,USP46-AS1:10,USP46-AS1:11 RNACentral:URS0000D5D6A5,RNACentral:URS0000D597A4,RNACentral:URS00009C1D68,RNACentral:URS0000D5E3DD,RNACentral:URS0000D5C6C1,RNACentral:URS0000D5A550,RNACentral:URS00008B8402,RNACentral:URS00009BDDEB,RNACentral:URS0000D57F01,RNACentral:URS0000D58E33,RNACentral:URS0000D5C70E lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,exon,exon,exon,exon,exon,intron,exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1321312428 Functional Loss SNV dbSNP153 33..33 33 - - - 48486 RMVar_ID_48486 Human_SNP_ID_184125052 A-to-I Human chr4 - 53054933 53054933 53054933 AGTTGGACTTCAGGCCAGGGACAATGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAAGT AGTTGGACTTCAGGCCAGGGACAATGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAAGT T C SCFD2 Ensembl:ENSG00000184178 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs562445226 Functional Loss SNV dbSNP153 33..33 33 - - - 48487 RMVar_ID_48487 Human_SNP_ID_184177256 A-to-I Human chr4 - 53267729 53267729 53267729 TTGAAAGACTGAGGAACCCCAGGCATGGTGATACACATCTGTAGTTTCAGCTACTCAGGAGGCTG TTGAAAGACTGAGGAACCCCAGGCATGGTGATGCACATCTGTAGTTTCAGCTACTCAGGAGGCTG T C SCFD2 Ensembl:ENSG00000184178 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1287522572 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15171198 RMVar_hsa_circ_58124,RMVar_hsa_circ_302198,RMVar_hsa_circ_86530,RMVar_hsa_circ_226037 48488 RMVar_ID_48488 Human_SNP_ID_184200405 A-to-I Human chr4 - 53357346 53357346 53357346 CAGCTCACTGAAACCTCCGCCTCTTGGATTCAAGCGATTCTTGTGCCTCAGCCTCCTGAGTGGCT CAGCTCACTGAAACCTCCGCCTCTTGGATTCATGCGATTCTTGTGCCTCAGCCTCCTGAGTGGCT T A SCFD2 Ensembl:ENSG00000184178 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs988716303 Functional Loss SNV dbSNP153 33..33 33 - - - 48489 RMVar_ID_48489 Human_SNP_ID_184206296 A-to-I Human chr4 - 53382287 53382287 53382287 TTTTCAGCAGTTTCATCTTCAATTCCAGATGGAGGATTAGCACTACAAACAACAAAAGTAAGTAT TTTTCAGCAGTTTCATCTTCAATTCCAGATGGTGGATTAGCACTACAAACAACAAAAGTAAGTAT T A - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1306615118 Functional Loss SNV dbSNP153 33..33 33 - - - 48490 RMVar_ID_48490 Human_SNP_ID_184216288 A-to-I Human chr4 + 53419540 53419539 53419540 ATAGCTCCCTGCAAACTCGAACTACCAGGCTCAAGCAGTCCTCCCATCTCAGCCTCCCGAGTAGC ATAGCTCCCTGCAAACTCGAACTACCAGGCTC_AGCAGTCCTCCCATCTCAGCCTCCCGAGTAGC CA C FIP1L1,AC058822.1 Ensembl:ENSG00000145216,Ensembl:ENSG00000282278 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444811250 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_324239,RMVar_hsa_circ_226042,RMVar_hsa_circ_78148,RMVar_hsa_circ_325445,RMVar_hsa_circ_69737,RMVar_hsa_circ_66202,RMVar_hsa_circ_226047,RMVar_hsa_circ_281182,RMVar_hsa_circ_121364,RMVar_hsa_circ_69438,RMVar_hsa_circ_226045,RMVar_hsa_circ_350479,RMVar_hsa_circ_287073,RMVar_hsa_circ_58831,RMVar_hsa_circ_277246,RMVar_hsa_circ_226048,RMVar_hsa_circ_78551,RMVar_hsa_circ_30466,RMVar_hsa_circ_86456,RMVar_hsa_circ_226046,RMVar_hsa_circ_122298,RMVar_hsa_circ_226054,RMVar_hsa_circ_92409,RMVar_hsa_circ_226055,RMVar_hsa_circ_226056,RMVar_hsa_circ_226057,RMVar_hsa_circ_331362,RMVar_hsa_circ_269880,RMVar_hsa_circ_283039,RMVar_hsa_circ_56112,RMVar_hsa_circ_226060,RMVar_hsa_circ_32210,RMVar_hsa_circ_278892,RMVar_hsa_circ_226059,RMVar_hsa_circ_288522,RMVar_hsa_circ_275829,RMVar_hsa_circ_226062,RMVar_hsa_circ_226063,RMVar_hsa_circ_226064 48491 RMVar_ID_48491 Human_SNP_ID_184363432 A-to-I Human chr4 - 54033179 54033179 54033179 TCTGTTCTTGCATTGCTATAAGGAAATACCTGAGACTGGATAATTTATAATGAAGAGGTTTAATT TCTGTTCTTGCATTGCTATAAGGAAATACCTGGGACTGGATAATTTATAATGAAGAGGTTTAATT T C CHIC2 Ensembl:ENSG00000109220 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1193060409 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_348787 48492 RMVar_ID_48492 Human_SNP_ID_184422388 A-to-I Human chr4 + 54260210 54260210 54260210 GCACTCCAGCCTGGGTGACAGAGCAAGACTCCATCTCATAAAAATAAAGAAATAAATAAACAAAT GCACTCCAGCCTGGGTGACAGAGCAAGACTCCGTCTCATAAAAATAAAGAAATAAATAAACAAAT A G PDGFRA,AC058822.1 Ensembl:ENSG00000134853,Ensembl:ENSG00000282278 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1560465710 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2673,RMVar_hsa_circ_119431,RMVar_hsa_circ_226069,RMVar_hsa_circ_308715 48493 RMVar_ID_48493 Human_SNP_ID_184703212 A-to-I Human chr4 + 55361407 55361407 55361407 GGTAGGCTGAGGAGAGAGAATTGCTTGAACCCAAGAGGCAGAGGTTGCAGTGAGCCAAGATTGTA GGTAGGCTGAGGAGAGAGAATTGCTTGAACCCTAGAGGCAGAGGTTGCAGTGAGCCAAGATTGTA A T SRD5A3 Ensembl:ENSG00000128039 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs771504545 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113584,RMVar_hsa_circ_315367,RMVar_hsa_circ_226105,RMVar_hsa_circ_331125,RMVar_hsa_circ_226106 48494 RMVar_ID_48494 Human_SNP_ID_184712894 A-to-I Human chr4 + 55400644 55400644 55400644 TATTTTTAGTAGAGACGAGGTTTTACCGTGTTAGCCAGGAGGTCTCCATCTCCTGACCTGGTGAT TATTTTTAGTAGAGACGAGGTTTTACCGTGTTGGCCAGGAGGTCTCCATCTCCTGACCTGGTGAT A G TMEM165 Ensembl:ENSG00000134851 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1297242952 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2851974,Human_RBP_ID_15173505 RMVar_hsa_circ_81518,RMVar_hsa_circ_226108 48495 RMVar_ID_48495 Human_SNP_ID_184713195 A-to-I Human chr4 + 55401933 55401933 55401933 GAGGTCAAGAGTTCTAGACCAGCCTGGCCAACATGATGAAACCCCATCTCTACTGAAAATACAAA GAGGTCAAGAGTTCTAGACCAGCCTGGCCAACGTGATGAAACCCCATCTCTACTGAAAATACAAA A G TMEM165 Ensembl:ENSG00000134851 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1300822918 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81518,RMVar_hsa_circ_226108 48496 RMVar_ID_48496 Human_SNP_ID_184713200 A-to-I Human chr4 + 55401952 55401952 55401952 CAGCCTGGCCAACATGATGAAACCCCATCTCTACTGAAAATACAAAAAATTAGCTGGGCGTGGTG CAGCCTGGCCAACATGATGAAACCCCATCTCTCCTGAAAATACAAAAAATTAGCTGGGCGTGGTG A C TMEM165 Ensembl:ENSG00000134851 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1414191978 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81518,RMVar_hsa_circ_226108 48497 RMVar_ID_48497 Human_SNP_ID_184714218 A-to-I Human chr4 + 55404305 55404305 55404305 CCAAAGTGCTGGGATGACAGGCGTGAGCCACCATGCCCAGCCATATTAGTTTCTTCAGTTTTATA CCAAAGTGCTGGGATGACAGGCGTGAGCCACCGTGCCCAGCCATATTAGTTTCTTCAGTTTTATA A G TMEM165 Ensembl:ENSG00000134851 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2459220 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_81518,RMVar_hsa_circ_226110,RMVar_hsa_circ_293035,RMVar_hsa_circ_226108,RMVar_hsa_circ_358053,RMVar_hsa_circ_280424,RMVar_hsa_circ_226109 48498 RMVar_ID_48498 Human_SNP_ID_184716354 A-to-I Human chr4 + 55413016 55413016 55413016 TTTATTTTTTTTTAGAGACTGAGTCTTGCTCTATCACTCAGGCTGGAGTGCAGTGGCATGATCAT TTTATTTTTTTTTAGAGACTGAGTCTTGCTCTGTCACTCAGGCTGGAGTGCAGTGGCATGATCAT A G TMEM165 Ensembl:ENSG00000134851 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs867691775 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77017,RMVar_hsa_circ_226110,RMVar_hsa_circ_293035,RMVar_hsa_circ_358053,RMVar_hsa_circ_285140,RMVar_hsa_circ_273989,RMVar_hsa_circ_226111,RMVar_hsa_circ_226113,RMVar_hsa_circ_226114,RMVar_hsa_circ_226112 48499 RMVar_ID_48499 Human_SNP_ID_184716358 A-to-I Human chr4 + 55413035 55413035 55413035 TGAGTCTTGCTCTATCACTCAGGCTGGAGTGCAGTGGCATGATCATAGCTCACTGAGACCTGGAA TGAGTCTTGCTCTATCACTCAGGCTGGAGTGCGGTGGCATGATCATAGCTCACTGAGACCTGGAA A G TMEM165 Ensembl:ENSG00000134851 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs909200573 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77017,RMVar_hsa_circ_226110,RMVar_hsa_circ_293035,RMVar_hsa_circ_358053,RMVar_hsa_circ_285140,RMVar_hsa_circ_273989,RMVar_hsa_circ_226111,RMVar_hsa_circ_226113,RMVar_hsa_circ_226114,RMVar_hsa_circ_226112 48500 RMVar_ID_48500 Human_SNP_ID_184716369 A-to-I Human chr4 + 55413079 55413079 55413079 ATAGCTCACTGAGACCTGGAACTCCTGGGCTCAAGTGATCCTTCCACCTCAGCCTCCTGAGTAGC ATAGCTCACTGAGACCTGGAACTCCTGGGCTCGAGTGATCCTTCCACCTCAGCCTCCTGAGTAGC A G TMEM165 Ensembl:ENSG00000134851 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1282429818 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77017,RMVar_hsa_circ_226110,RMVar_hsa_circ_293035,RMVar_hsa_circ_358053,RMVar_hsa_circ_285140,RMVar_hsa_circ_273989,RMVar_hsa_circ_226111,RMVar_hsa_circ_226113,RMVar_hsa_circ_226114,RMVar_hsa_circ_226112 48501 RMVar_ID_48501 Human_SNP_ID_184716432 A-to-I Human chr4 + 55413385 55413385 55413385 CACCCAGGCCGGAGTGCAGTGGCATGATCCCGACTCACTTAAACCTCCATCTCCCAGGCTCAGGC CACCCAGGCCGGAGTGCAGTGGCATGATCCCGGCTCACTTAAACCTCCATCTCCCAGGCTCAGGC A G TMEM165 Ensembl:ENSG00000134851 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7692795 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77017,RMVar_hsa_circ_226110,RMVar_hsa_circ_293035,RMVar_hsa_circ_358053,RMVar_hsa_circ_285140,RMVar_hsa_circ_273989,RMVar_hsa_circ_226111,RMVar_hsa_circ_226113,RMVar_hsa_circ_226114,RMVar_hsa_circ_226112 48502 RMVar_ID_48502 Human_SNP_ID_184716435 A-to-I Human chr4 + 55413408 55413408 55413408 ATGATCCCGACTCACTTAAACCTCCATCTCCCAGGCTCAGGCGATTTTCCTGCCTCAGCCTCCCA ATGATCCCGACTCACTTAAACCTCCATCTCCCGGGCTCAGGCGATTTTCCTGCCTCAGCCTCCCA A G TMEM165 Ensembl:ENSG00000134851 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1214125601 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15173960 RMVar_hsa_circ_77017,RMVar_hsa_circ_226110,RMVar_hsa_circ_293035,RMVar_hsa_circ_358053,RMVar_hsa_circ_285140,RMVar_hsa_circ_273989,RMVar_hsa_circ_226111,RMVar_hsa_circ_226113,RMVar_hsa_circ_226114,RMVar_hsa_circ_226112 48503 RMVar_ID_48503 Human_SNP_ID_184716608 A-to-I Human chr4 + 55414090 55414090 55414090 GGAGATCGAGGCCATCCTGGCTAACACGGTGAAACCCCGTCTCTACTAAAAAAATCCAAAAAACT GGAGATCGAGGCCATCCTGGCTAACACGGTGATACCCCGTCTCTACTAAAAAAATCCAAAAAACT A T TMEM165 Ensembl:ENSG00000134851 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs951116517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_160577 RMVar_hsa_circ_77017,RMVar_hsa_circ_226110,RMVar_hsa_circ_293035,RMVar_hsa_circ_358053,RMVar_hsa_circ_285140,RMVar_hsa_circ_273989,RMVar_hsa_circ_226111,RMVar_hsa_circ_226113,RMVar_hsa_circ_226114,RMVar_hsa_circ_226112 48504 RMVar_ID_48504 Human_SNP_ID_184717016 A-to-I Human chr4 + 55415910 55415910 55415910 GGGATCTCACTCTGTTGCCCAAGCTGGGATGCAGTGGCATGATCGCAGCTCACTGCAGCTTTGAC GGGATCTCACTCTGTTGCCCAAGCTGGGATGCGGTGGCATGATCGCAGCTCACTGCAGCTTTGAC A G TMEM165 Ensembl:ENSG00000134851 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1042137436 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77017,RMVar_hsa_circ_226110,RMVar_hsa_circ_293035,RMVar_hsa_circ_358053,RMVar_hsa_circ_285140,RMVar_hsa_circ_273989,RMVar_hsa_circ_226111,RMVar_hsa_circ_226113,RMVar_hsa_circ_226114,RMVar_hsa_circ_226112 48505 RMVar_ID_48505 Human_SNP_ID_184717030 A-to-I Human chr4 + 55415995 55415995 55415995 TCCTATCTCAGCCCCTCAAGTAGGCTGGGACCAAGGCGTGTGTCACCCCGTCAGGCTAATTTTTG TCCTATCTCAGCCCCTCAAGTAGGCTGGGACCGAGGCGTGTGTCACCCCGTCAGGCTAATTTTTG A G TMEM165 Ensembl:ENSG00000134851 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs914958992 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5508102,Human_RBP_ID_15174046 RMVar_hsa_circ_77017,RMVar_hsa_circ_226110,RMVar_hsa_circ_293035,RMVar_hsa_circ_358053,RMVar_hsa_circ_285140,RMVar_hsa_circ_273989,RMVar_hsa_circ_226111,RMVar_hsa_circ_226113,RMVar_hsa_circ_226114,RMVar_hsa_circ_226112 48506 RMVar_ID_48506 Human_SNP_ID_184717057 A-to-I Human chr4 + 55416093 55416093 55416093 TGACCAGTGGTCTCAAGCTCCTGGGCTCAAGTAATCCGCCCGACTCGGTCTCCCAAAGTGCTGGG TGACCAGTGGTCTCAAGCTCCTGGGCTCAAGTGATCCGCCCGACTCGGTCTCCCAAAGTGCTGGG A G TMEM165 Ensembl:ENSG00000134851 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1027773339 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15174054,Human_RBP_ID_25815175 Human_Splice_Rec_562325 RMVar_hsa_circ_77017,RMVar_hsa_circ_226110,RMVar_hsa_circ_293035,RMVar_hsa_circ_358053,RMVar_hsa_circ_285140,RMVar_hsa_circ_273989,RMVar_hsa_circ_226111,RMVar_hsa_circ_226113,RMVar_hsa_circ_226114,RMVar_hsa_circ_226112 48507 RMVar_ID_48507 Human_SNP_ID_184717762 A-to-I Human chr4 + 55418898 55418898 55418898 GAGAAACCCCTACTACTAAAAATACAAAAATTAGCCGGGCAAGGTGGCTCATGCCTGTAATCTTA GAGAAACCCCTACTACTAAAAATACAAAAATTTGCCGGGCAAGGTGGCTCATGCCTGTAATCTTA A T TMEM165 Ensembl:ENSG00000134851 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs919493662 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18027664 RMVar_hsa_circ_77017,RMVar_hsa_circ_358053,RMVar_hsa_circ_285140,RMVar_hsa_circ_226111,RMVar_hsa_circ_226112,RMVar_hsa_circ_373985,RMVar_hsa_circ_226117,RMVar_hsa_circ_226118,RMVar_hsa_circ_329937,RMVar_hsa_circ_118032 48508 RMVar_ID_48508 Human_SNP_ID_184718519 A-to-I Human chr4 + 55421505 55421505 55421505 TTTTTTGTAGAGACAGGGTTTTGCCATGTTGCAGAGGCTGGTCTCGAACTCCTGAGTTCATGCAA TTTTTTGTAGAGACAGGGTTTTGCCATGTTGCCGAGGCTGGTCTCGAACTCCTGAGTTCATGCAA A C TMEM165 Ensembl:ENSG00000134851 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1164523003 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15174223,Human_RBP_ID_17574619 RMVar_hsa_circ_77017,RMVar_hsa_circ_358053,RMVar_hsa_circ_285140,RMVar_hsa_circ_226111,RMVar_hsa_circ_226112,RMVar_hsa_circ_373985,RMVar_hsa_circ_226117,RMVar_hsa_circ_226118,RMVar_hsa_circ_329937,RMVar_hsa_circ_118032 48509 RMVar_ID_48509 Human_SNP_ID_184718732 A-to-I Human chr4 + 55422311 55422311 55422311 TGAGAGTCTTGCTCTGTCACCCAGGCTGGAGTACAGTGGCACAATCTTGGCTTGCTGCAACCTCT TGAGAGTCTTGCTCTGTCACCCAGGCTGGAGTGCAGTGGCACAATCTTGGCTTGCTGCAACCTCT A G TMEM165 Ensembl:ENSG00000134851 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1345638542 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77017,RMVar_hsa_circ_358053,RMVar_hsa_circ_285140,RMVar_hsa_circ_226111,RMVar_hsa_circ_226112,RMVar_hsa_circ_373985,RMVar_hsa_circ_226117,RMVar_hsa_circ_226118,RMVar_hsa_circ_329937,RMVar_hsa_circ_118032 48510 RMVar_ID_48510 Human_SNP_ID_184718736 A-to-I Human chr4 + 55422321 55422321 55422321 GCTCTGTCACCCAGGCTGGAGTACAGTGGCACAATCTTGGCTTGCTGCAACCTCTGCTTCCTGGG GCTCTGTCACCCAGGCTGGAGTACAGTGGCACGATCTTGGCTTGCTGCAACCTCTGCTTCCTGGG A G TMEM165 Ensembl:ENSG00000134851 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1279542274 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24058894 RMVar_hsa_circ_77017,RMVar_hsa_circ_358053,RMVar_hsa_circ_285140,RMVar_hsa_circ_226111,RMVar_hsa_circ_226112,RMVar_hsa_circ_373985,RMVar_hsa_circ_226117,RMVar_hsa_circ_226118,RMVar_hsa_circ_329937,RMVar_hsa_circ_118032 48511 RMVar_ID_48511 Human_SNP_ID_184718879 A-to-I Human chr4 + 55422897 55422897 55422897 TGACCTCGTGATCCACCCTCCTCGGCCTCCCAAAGTGCTGGCATTACAGGCGTGAGCCACTGCAC TGACCTCGTGATCCACCCTCCTCGGCCTCCCAGAGTGCTGGCATTACAGGCGTGAGCCACTGCAC A G TMEM165 Ensembl:ENSG00000134851 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1331239876 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77017,RMVar_hsa_circ_358053,RMVar_hsa_circ_285140,RMVar_hsa_circ_226111,RMVar_hsa_circ_226112,RMVar_hsa_circ_373985,RMVar_hsa_circ_226117,RMVar_hsa_circ_226118,RMVar_hsa_circ_329937,RMVar_hsa_circ_118032 48512 RMVar_ID_48512 Human_SNP_ID_184719060 A-to-I Human chr4 + 55423612 55423611 55423612 GCCTGGCTAATTTTTAATTTTTTTGTAGAGACAAGGTCTCACTGTGTTGCCTAGGCTAGTCTCAA GCCTGGCTAATTTTTAATTTTTTTGTAGAGATGAGGTCTCACTGTGTTGCCTAGGCTAGTCTCAA CA TG TMEM165 Ensembl:ENSG00000134851 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs71639512 Functional Loss MNV dbSNP153 32..33 33 - - - Human_RBP_ID_15174316 RMVar_hsa_circ_77017,RMVar_hsa_circ_358053,RMVar_hsa_circ_285140,RMVar_hsa_circ_226111,RMVar_hsa_circ_226112,RMVar_hsa_circ_373985,RMVar_hsa_circ_226117,RMVar_hsa_circ_226118,RMVar_hsa_circ_329937,RMVar_hsa_circ_118032 48513 RMVar_ID_48513 Human_SNP_ID_184719061 A-to-I Human chr4 + 55423612 55423611 55423612 GCCTGGCTAATTTTTAATTTTTTTGTAGAGACAAGGTCTCACTGTGTTGCCTAGGCTAGTCTCAA GCCTGGCTAATTTTTAATTTTTTTGTAGAGAC_AGGTCTCACTGTGTTGCCTAGGCTAGTCTCAA CA C TMEM165 Ensembl:ENSG00000134851 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1553887236 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_15174316 RMVar_hsa_circ_77017,RMVar_hsa_circ_358053,RMVar_hsa_circ_285140,RMVar_hsa_circ_226111,RMVar_hsa_circ_226112,RMVar_hsa_circ_373985,RMVar_hsa_circ_226117,RMVar_hsa_circ_226118,RMVar_hsa_circ_329937,RMVar_hsa_circ_118032 48514 RMVar_ID_48514 Human_SNP_ID_184719062 A-to-I Human chr4 + 55423612 55423612 55423612 GCCTGGCTAATTTTTAATTTTTTTGTAGAGACAAGGTCTCACTGTGTTGCCTAGGCTAGTCTCAA GCCTGGCTAATTTTTAATTTTTTTGTAGAGACGAGGTCTCACTGTGTTGCCTAGGCTAGTCTCAA A G TMEM165 Ensembl:ENSG00000134851 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs530875 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15174316 RMVar_hsa_circ_77017,RMVar_hsa_circ_358053,RMVar_hsa_circ_285140,RMVar_hsa_circ_226111,RMVar_hsa_circ_226112,RMVar_hsa_circ_373985,RMVar_hsa_circ_226117,RMVar_hsa_circ_226118,RMVar_hsa_circ_329937,RMVar_hsa_circ_118032 48515 RMVar_ID_48515 Human_SNP_ID_184719070 A-to-I Human chr4 + 55423637 55423637 55423637 TAGAGACAAGGTCTCACTGTGTTGCCTAGGCTAGTCTCAAACTGCCAGGCTCAAGCAATCCTCTT TAGAGACAAGGTCTCACTGTGTTGCCTAGGCTGGTCTCAAACTGCCAGGCTCAAGCAATCCTCTT A G TMEM165 Ensembl:ENSG00000134851 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1460523639 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77017,RMVar_hsa_circ_358053,RMVar_hsa_circ_285140,RMVar_hsa_circ_226111,RMVar_hsa_circ_226112,RMVar_hsa_circ_373985,RMVar_hsa_circ_226117,RMVar_hsa_circ_226118,RMVar_hsa_circ_329937,RMVar_hsa_circ_118032 48516 RMVar_ID_48516 Human_SNP_ID_184719114 A-to-I Human chr4 + 55423832 55423832 55423832 ACTCCAAGATGATAGGGTCCTCCCTCACCTGGACTCCCACCTACCCTCATGACCTCCTTTTGTGA ACTCCAAGATGATAGGGTCCTCCCTCACCTGGGCTCCCACCTACCCTCATGACCTCCTTTTGTGA A G TMEM165 Ensembl:ENSG00000134851 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs532768 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5834,GWAS_ID_5835,GWAS_ID_5836,GWAS_ID_5837,GWAS_ID_5838,GWAS_ID_5839,GWAS_ID_5840,GWAS_ID_5841 RMVar_hsa_circ_77017,RMVar_hsa_circ_358053,RMVar_hsa_circ_285140,RMVar_hsa_circ_226111,RMVar_hsa_circ_226112,RMVar_hsa_circ_373985,RMVar_hsa_circ_226117,RMVar_hsa_circ_226118,RMVar_hsa_circ_329937,RMVar_hsa_circ_118032 48517 RMVar_ID_48517 Human_SNP_ID_184719115 A-to-I Human chr4 + 55423832 55423832 55423832 ACTCCAAGATGATAGGGTCCTCCCTCACCTGGACTCCCACCTACCCTCATGACCTCCTTTTGTGA ACTCCAAGATGATAGGGTCCTCCCTCACCTGGTCTCCCACCTACCCTCATGACCTCCTTTTGTGA A T TMEM165 Ensembl:ENSG00000134851 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs532768 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5834,GWAS_ID_5835,GWAS_ID_5836,GWAS_ID_5837,GWAS_ID_5838,GWAS_ID_5839,GWAS_ID_5840,GWAS_ID_5841 RMVar_hsa_circ_77017,RMVar_hsa_circ_358053,RMVar_hsa_circ_285140,RMVar_hsa_circ_226111,RMVar_hsa_circ_226112,RMVar_hsa_circ_373985,RMVar_hsa_circ_226117,RMVar_hsa_circ_226118,RMVar_hsa_circ_329937,RMVar_hsa_circ_118032 48518 RMVar_ID_48518 Human_SNP_ID_184724697 A-to-I Human chr4 - 55445651 55445651 55445651 AGAAAGTTAAGGCTGTAGAGAGCCATGATCGCACCACTGCTTTCCAGCCTGGGTGACAGAGTGAG AGAAAGTTAAGGCTGTAGAGAGCCATGATCGCCCCACTGCTTTCCAGCCTGGGTGACAGAGTGAG T G CLOCK Ensembl:ENSG00000134852 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1403338599 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25835060 RMVar_hsa_circ_73858,RMVar_hsa_circ_97586,RMVar_hsa_circ_99357,RMVar_hsa_circ_226123,RMVar_hsa_circ_226122,RMVar_hsa_circ_279227,RMVar_hsa_circ_64179,RMVar_hsa_circ_3390,RMVar_hsa_circ_34881,RMVar_hsa_circ_226124,RMVar_hsa_circ_325088 48519 RMVar_ID_48519 Human_SNP_ID_184733480 A-to-I Human chr4 - 55481060 55481059 55481060 TAATATTGCTCCTAGGGTTGAGTTAGCCACCAATGCTCTTGATTTTATTTTTTAGGAATGGTCTT TAATATTGCTCCTAGGGTTGAGTTAGCCACCA_TGCTCTTGATTTTATTTTTTAGGAATGGTCTT AT A CLOCK Ensembl:ENSG00000134852 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1443181192 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_21814,RMVar_hsa_circ_97586,RMVar_hsa_circ_226123,RMVar_hsa_circ_279227,RMVar_hsa_circ_226124,RMVar_hsa_circ_333250,RMVar_hsa_circ_21803,RMVar_hsa_circ_226125,RMVar_hsa_circ_30126,RMVar_hsa_circ_10217,RMVar_hsa_circ_66786,RMVar_hsa_circ_226139,RMVar_hsa_circ_289205,RMVar_hsa_circ_226135,RMVar_hsa_circ_319108,RMVar_hsa_circ_319446,RMVar_hsa_circ_311827,RMVar_hsa_circ_226133,RMVar_hsa_circ_226134,RMVar_hsa_circ_290385,RMVar_hsa_circ_114662,RMVar_hsa_circ_285107,RMVar_hsa_circ_27886,RMVar_hsa_circ_226137,RMVar_hsa_circ_226138,RMVar_hsa_circ_226136,RMVar_hsa_circ_8275,RMVar_hsa_circ_27477,RMVar_hsa_circ_226141 48520 RMVar_ID_48520 Human_SNP_ID_184733481 A-to-I Human chr4 - 55481060 55481060 55481060 TAATATTGCTCCTAGGGTTGAGTTAGCCACCAATGCTCTTGATTTTATTTTTTAGGAATGGTCTT TAATATTGCTCCTAGGGTTGAGTTAGCCACCATTGCTCTTGATTTTATTTTTTAGGAATGGTCTT T A CLOCK Ensembl:ENSG00000134852 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs9997288 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_133,Clinvar_Rec_134 GWAS_ID_5842,GWAS_ID_5843,GWAS_ID_5844,GWAS_ID_5845,GWAS_ID_5846,GWAS_ID_5847,GWAS_ID_5848,GWAS_ID_5849,GWAS_ID_5850,GWAS_ID_5851,GWAS_ID_5852,GWAS_ID_5853,GWAS_ID_5854,GWAS_ID_5855,GWAS_ID_5856,GWAS_ID_5857,GWAS_ID_5858,GWAS_ID_5859,GWAS_ID_5860,GWAS_ID_5861,GWAS_ID_5862,GWAS_ID_5863,GWAS_ID_5864,GWAS_ID_5865,GWAS_ID_5866,GWAS_ID_5867,GWAS_ID_5868,GWAS_ID_5869,GWAS_ID_5870,GWAS_ID_5871,GWAS_ID_5872,GWAS_ID_5873,GWAS_ID_5874,GWAS_ID_5875,GWAS_ID_5876,GWAS_ID_5877,GWAS_ID_5878,GWAS_ID_5879,GWAS_ID_5880,GWAS_ID_5881,GWAS_ID_5882,GWAS_ID_5883,GWAS_ID_5884,GWAS_ID_5885,GWAS_ID_5886,GWAS_ID_5887,GWAS_ID_5888,GWAS_ID_5889,GWAS_ID_5890,GWAS_ID_5891,GWAS_ID_5892,GWAS_ID_5893,GWAS_ID_5894,GWAS_ID_5895,GWAS_ID_5896,GWAS_ID_5897,GWAS_ID_5898,GWAS_ID_5899,GWAS_ID_5900,GWAS_ID_5901,GWAS_ID_5902,GWAS_ID_5903,GWAS_ID_5904,GWAS_ID_5905,GWAS_ID_5906,GWAS_ID_5907,GWAS_ID_5908,GWAS_ID_5909,GWAS_ID_5910,GWAS_ID_5911,GWAS_ID_5912,GWAS_ID_5913,GWAS_ID_5914,GWAS_ID_5915,GWAS_ID_5916,GWAS_ID_5917,GWAS_ID_5918,GWAS_ID_5919,GWAS_ID_5920,GWAS_ID_5921,GWAS_ID_5922 RMVar_hsa_circ_21814,RMVar_hsa_circ_97586,RMVar_hsa_circ_226123,RMVar_hsa_circ_279227,RMVar_hsa_circ_226124,RMVar_hsa_circ_333250,RMVar_hsa_circ_21803,RMVar_hsa_circ_226125,RMVar_hsa_circ_30126,RMVar_hsa_circ_10217,RMVar_hsa_circ_66786,RMVar_hsa_circ_226139,RMVar_hsa_circ_289205,RMVar_hsa_circ_226135,RMVar_hsa_circ_319108,RMVar_hsa_circ_319446,RMVar_hsa_circ_311827,RMVar_hsa_circ_226133,RMVar_hsa_circ_226134,RMVar_hsa_circ_290385,RMVar_hsa_circ_114662,RMVar_hsa_circ_285107,RMVar_hsa_circ_27886,RMVar_hsa_circ_226137,RMVar_hsa_circ_226138,RMVar_hsa_circ_226136,RMVar_hsa_circ_8275,RMVar_hsa_circ_27477,RMVar_hsa_circ_226141 48521 RMVar_ID_48521 Human_SNP_ID_184733482 A-to-I Human chr4 - 55481060 55481060 55481060 TAATATTGCTCCTAGGGTTGAGTTAGCCACCAATGCTCTTGATTTTATTTTTTAGGAATGGTCTT TAATATTGCTCCTAGGGTTGAGTTAGCCACCAGTGCTCTTGATTTTATTTTTTAGGAATGGTCTT T C CLOCK Ensembl:ENSG00000134852 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs9997288 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_133,Clinvar_Rec_134 GWAS_ID_5842,GWAS_ID_5843,GWAS_ID_5844,GWAS_ID_5845,GWAS_ID_5846,GWAS_ID_5847,GWAS_ID_5848,GWAS_ID_5849,GWAS_ID_5850,GWAS_ID_5851,GWAS_ID_5852,GWAS_ID_5853,GWAS_ID_5854,GWAS_ID_5855,GWAS_ID_5856,GWAS_ID_5857,GWAS_ID_5858,GWAS_ID_5859,GWAS_ID_5860,GWAS_ID_5861,GWAS_ID_5862,GWAS_ID_5863,GWAS_ID_5864,GWAS_ID_5865,GWAS_ID_5866,GWAS_ID_5867,GWAS_ID_5868,GWAS_ID_5869,GWAS_ID_5870,GWAS_ID_5871,GWAS_ID_5872,GWAS_ID_5873,GWAS_ID_5874,GWAS_ID_5875,GWAS_ID_5876,GWAS_ID_5877,GWAS_ID_5878,GWAS_ID_5879,GWAS_ID_5880,GWAS_ID_5881,GWAS_ID_5882,GWAS_ID_5883,GWAS_ID_5884,GWAS_ID_5885,GWAS_ID_5886,GWAS_ID_5887,GWAS_ID_5888,GWAS_ID_5889,GWAS_ID_5890,GWAS_ID_5891,GWAS_ID_5892,GWAS_ID_5893,GWAS_ID_5894,GWAS_ID_5895,GWAS_ID_5896,GWAS_ID_5897,GWAS_ID_5898,GWAS_ID_5899,GWAS_ID_5900,GWAS_ID_5901,GWAS_ID_5902,GWAS_ID_5903,GWAS_ID_5904,GWAS_ID_5905,GWAS_ID_5906,GWAS_ID_5907,GWAS_ID_5908,GWAS_ID_5909,GWAS_ID_5910,GWAS_ID_5911,GWAS_ID_5912,GWAS_ID_5913,GWAS_ID_5914,GWAS_ID_5915,GWAS_ID_5916,GWAS_ID_5917,GWAS_ID_5918,GWAS_ID_5919,GWAS_ID_5920,GWAS_ID_5921,GWAS_ID_5922 RMVar_hsa_circ_21814,RMVar_hsa_circ_97586,RMVar_hsa_circ_226123,RMVar_hsa_circ_279227,RMVar_hsa_circ_226124,RMVar_hsa_circ_333250,RMVar_hsa_circ_21803,RMVar_hsa_circ_226125,RMVar_hsa_circ_30126,RMVar_hsa_circ_10217,RMVar_hsa_circ_66786,RMVar_hsa_circ_226139,RMVar_hsa_circ_289205,RMVar_hsa_circ_226135,RMVar_hsa_circ_319108,RMVar_hsa_circ_319446,RMVar_hsa_circ_311827,RMVar_hsa_circ_226133,RMVar_hsa_circ_226134,RMVar_hsa_circ_290385,RMVar_hsa_circ_114662,RMVar_hsa_circ_285107,RMVar_hsa_circ_27886,RMVar_hsa_circ_226137,RMVar_hsa_circ_226138,RMVar_hsa_circ_226136,RMVar_hsa_circ_8275,RMVar_hsa_circ_27477,RMVar_hsa_circ_226141 48522 RMVar_ID_48522 Human_SNP_ID_184739866 A-to-I Human chr4 - 55507134 55507134 55507134 ACTTTGTTTATTTTTTGTAGAGATGAGGTTTCACTATGCTGCTTAGGCTGCTCTAGAACTCCTGG ACTTTGTTTATTTTTTGTAGAGATGAGGTTTCGCTATGCTGCTTAGGCTGCTCTAGAACTCCTGG T C CLOCK Ensembl:ENSG00000134852 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1164249316 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15175073 RMVar_hsa_circ_21814,RMVar_hsa_circ_279227,RMVar_hsa_circ_226124,RMVar_hsa_circ_333250,RMVar_hsa_circ_226125,RMVar_hsa_circ_10217,RMVar_hsa_circ_66786,RMVar_hsa_circ_226135,RMVar_hsa_circ_319446,RMVar_hsa_circ_290385,RMVar_hsa_circ_114662,RMVar_hsa_circ_226137,RMVar_hsa_circ_226136,RMVar_hsa_circ_27477,RMVar_hsa_circ_226144,RMVar_hsa_circ_226143,RMVar_hsa_circ_348634,RMVar_hsa_circ_326892,RMVar_hsa_circ_226145,RMVar_hsa_circ_276031 48523 RMVar_ID_48523 Human_SNP_ID_184749437 A-to-I Human chr4 - 55543176 55543176 55543176 TCTGGTATAGATTTAATTCACTGTAAACTTCGAGCGGCCGAGGTGGGAGAATGGCTTGAGCCCAG TCTGGTATAGATTTAATTCACTGTAAACTTCGTGCGGCCGAGGTGGGAGAATGGCTTGAGCCCAG T A CLOCK Ensembl:ENSG00000134852 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388008849 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15175563 RMVar_hsa_circ_114662,RMVar_hsa_circ_226136 48524 RMVar_ID_48524 Human_SNP_ID_184749438 A-to-I Human chr4 - 55543176 55543176 55543176 TCTGGTATAGATTTAATTCACTGTAAACTTCGAGCGGCCGAGGTGGGAGAATGGCTTGAGCCCAG TCTGGTATAGATTTAATTCACTGTAAACTTCGGGCGGCCGAGGTGGGAGAATGGCTTGAGCCCAG T C CLOCK Ensembl:ENSG00000134852 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388008849 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15175563 RMVar_hsa_circ_114662,RMVar_hsa_circ_226136 48525 RMVar_ID_48525 Human_SNP_ID_184749439 A-to-I Human chr4 - 55543176 55543176 55543176 TCTGGTATAGATTTAATTCACTGTAAACTTCGAGCGGCCGAGGTGGGAGAATGGCTTGAGCCCAG TCTGGTATAGATTTAATTCACTGTAAACTTCGCGCGGCCGAGGTGGGAGAATGGCTTGAGCCCAG T G CLOCK Ensembl:ENSG00000134852 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388008849 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15175563 RMVar_hsa_circ_114662,RMVar_hsa_circ_226136 48526 RMVar_ID_48526 Human_SNP_ID_184833290 A-to-I Human chr4 + 55894842 55894842 55894842 TGGGGTTTCTCCATGTTGGTCATGCTGGTCTCAAACTCCCAACCTCAGGTGATCTGCCCACCTCA TGGGGTTTCTCCATGTTGGTCATGCTGGTCTCTAACTCCCAACCTCAGGTGATCTGCCCACCTCA A T EXOC1 Ensembl:ENSG00000090989 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs967026464 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_312980,RMVar_hsa_circ_116471,RMVar_hsa_circ_3704,RMVar_hsa_circ_226168,RMVar_hsa_circ_34422,RMVar_hsa_circ_226167,RMVar_hsa_circ_343407,RMVar_hsa_circ_349979,RMVar_hsa_circ_226170,RMVar_hsa_circ_54623,RMVar_hsa_circ_342144,RMVar_hsa_circ_281518,RMVar_hsa_circ_357770,RMVar_hsa_circ_226171,RMVar_hsa_circ_283062,RMVar_hsa_circ_354283,RMVar_hsa_circ_28508,RMVar_hsa_circ_226172 48527 RMVar_ID_48527 Human_SNP_ID_184848537 A-to-I Human chr4 + 55961594 55961594 55961594 GGCGACCAGCCTGACCAACATGGAGAAACCCTATCTCTACTAAAAATACAAAATTAGCCGGGTGT GGCGACCAGCCTGACCAACATGGAGAAACCCTGTCTCTACTAAAAATACAAAATTAGCCGGGTGT A G CEP135 Ensembl:ENSG00000174799 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs946135170 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9928,RMVar_hsa_circ_48488,RMVar_hsa_circ_20346,RMVar_hsa_circ_101962,RMVar_hsa_circ_226176,RMVar_hsa_circ_70325,RMVar_hsa_circ_287066,RMVar_hsa_circ_330413,RMVar_hsa_circ_59633,RMVar_hsa_circ_35964,RMVar_hsa_circ_44821,RMVar_hsa_circ_17086,RMVar_hsa_circ_226177,RMVar_hsa_circ_226179,RMVar_hsa_circ_226180,RMVar_hsa_circ_226178 48528 RMVar_ID_48528 Human_SNP_ID_184848540 A-to-I Human chr4 + 55961600 55961600 55961600 CAGCCTGACCAACATGGAGAAACCCTATCTCTACTAAAAATACAAAATTAGCCGGGTGTGGTGGC CAGCCTGACCAACATGGAGAAACCCTATCTCTTCTAAAAATACAAAATTAGCCGGGTGTGGTGGC A T CEP135 Ensembl:ENSG00000174799 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1208691140 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9928,RMVar_hsa_circ_48488,RMVar_hsa_circ_20346,RMVar_hsa_circ_101962,RMVar_hsa_circ_226176,RMVar_hsa_circ_70325,RMVar_hsa_circ_287066,RMVar_hsa_circ_330413,RMVar_hsa_circ_59633,RMVar_hsa_circ_35964,RMVar_hsa_circ_44821,RMVar_hsa_circ_17086,RMVar_hsa_circ_226177,RMVar_hsa_circ_226179,RMVar_hsa_circ_226180,RMVar_hsa_circ_226178 48529 RMVar_ID_48529 Human_SNP_ID_184848541 A-to-I Human chr4 + 55961603 55961603 55961603 CCTGACCAACATGGAGAAACCCTATCTCTACTAAAAATACAAAATTAGCCGGGTGTGGTGGCGCA CCTGACCAACATGGAGAAACCCTATCTCTACTGAAAATACAAAATTAGCCGGGTGTGGTGGCGCA A G CEP135 Ensembl:ENSG00000174799 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs545938695 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9928,RMVar_hsa_circ_48488,RMVar_hsa_circ_20346,RMVar_hsa_circ_101962,RMVar_hsa_circ_226176,RMVar_hsa_circ_70325,RMVar_hsa_circ_287066,RMVar_hsa_circ_330413,RMVar_hsa_circ_59633,RMVar_hsa_circ_35964,RMVar_hsa_circ_44821,RMVar_hsa_circ_17086,RMVar_hsa_circ_226177,RMVar_hsa_circ_226179,RMVar_hsa_circ_226180,RMVar_hsa_circ_226178 48530 RMVar_ID_48530 Human_SNP_ID_184848563 A-to-I Human chr4 + 55961713 55961713 55961713 TTGAACCCGGGAGGCAGAGGTTGTGGTGAGCCAAGATCACACCATTGCACTCCAGCCTGGGCAAC TTGAACCCGGGAGGCAGAGGTTGTGGTGAGCCGAGATCACACCATTGCACTCCAGCCTGGGCAAC A G CEP135 Ensembl:ENSG00000174799 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1241365709 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9928,RMVar_hsa_circ_48488,RMVar_hsa_circ_20346,RMVar_hsa_circ_101962,RMVar_hsa_circ_226176,RMVar_hsa_circ_70325,RMVar_hsa_circ_287066,RMVar_hsa_circ_330413,RMVar_hsa_circ_59633,RMVar_hsa_circ_35964,RMVar_hsa_circ_44821,RMVar_hsa_circ_17086,RMVar_hsa_circ_226177,RMVar_hsa_circ_226179,RMVar_hsa_circ_226180,RMVar_hsa_circ_226178 48531 RMVar_ID_48531 Human_SNP_ID_184848565 A-to-I Human chr4 + 55961721 55961721 55961721 GGGAGGCAGAGGTTGTGGTGAGCCAAGATCACACCATTGCACTCCAGCCTGGGCAACAAGAGCGA GGGAGGCAGAGGTTGTGGTGAGCCAAGATCACGCCATTGCACTCCAGCCTGGGCAACAAGAGCGA A G CEP135 Ensembl:ENSG00000174799 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1263787719 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25835084 RMVar_hsa_circ_9928,RMVar_hsa_circ_48488,RMVar_hsa_circ_20346,RMVar_hsa_circ_101962,RMVar_hsa_circ_226176,RMVar_hsa_circ_70325,RMVar_hsa_circ_287066,RMVar_hsa_circ_330413,RMVar_hsa_circ_59633,RMVar_hsa_circ_35964,RMVar_hsa_circ_44821,RMVar_hsa_circ_17086,RMVar_hsa_circ_226177,RMVar_hsa_circ_226179,RMVar_hsa_circ_226180,RMVar_hsa_circ_226178 48532 RMVar_ID_48532 Human_SNP_ID_184934764 A-to-I Human chr4 - 56331220 56331220 56331220 AAATTAAAAAAAAAAAAAGCTAAGTAGGGTCAAGCCTGGTTAGTACTTAGATGGGAGACCTCCTT AAATTAAAAAAAAAAAAAGCTAAGTAGGGTCAGGCCTGGTTAGTACTTAGATGGGAGACCTCCTT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1011408743 Functional Loss SNV dbSNP153 33..33 33 - - - 48533 RMVar_ID_48533 Human_SNP_ID_184939583 A-to-I Human chr4 - 56347744 56347744 56347744 GGACGTGCCACCACACCTGGCTAATGTTTGTAATTTTTGTAGAGACAGAGCTTCTGCGTGTTGTC GGACGTGCCACCACACCTGGCTAATGTTTGTACTTTTTGTAGAGACAGAGCTTCTGCGTGTTGTC T G AASDH Ensembl:ENSG00000157426 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1007040762 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11360,RMVar_hsa_circ_266257,RMVar_hsa_circ_71906 48534 RMVar_ID_48534 Human_SNP_ID_184956833 A-to-I Human chr4 - 56417584 56417584 56417584 TAGGCATGGGGTCTCACTGTGTTGCCCAGGCTAGTCTCGAACTCCTGGTCTCAAGTGATCCCGCA TAGGCATGGGGTCTCACTGTGTTGCCCAGGCTGGTCTCGAACTCCTGGTCTCAAGTGATCCCGCA T C PPAT Ensembl:ENSG00000128059 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1196450939 Functional Loss SNV dbSNP153 33..33 33 - - - 48535 RMVar_ID_48535 Human_SNP_ID_184967148 A-to-I Human chr4 + 56459912 56459912 56459912 TCTCCAGACTTGCATTTTTTTTTTTTTTTTTGAGACAGGGTCTCACTGTCGCCCAGGCTGGAGTG TCTCCAGACTTGCATTTTTTTTTTTTTTTTTGTGACAGGGTCTCACTGTCGCCCAGGCTGGAGTG A T PAICS Ensembl:ENSG00000128050 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-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 48536 RMVar_ID_48536 Human_SNP_ID_184967151 A-to-I Human chr4 + 56459916 56459916 56459916 CAGACTTGCATTTTTTTTTTTTTTTTTGAGACAGGGTCTCACTGTCGCCCAGGCTGGAGTGCAGT CAGACTTGCATTTTTTTTTTTTTTTTTGAGACGGGGTCTCACTGTCGCCCAGGCTGGAGTGCAGT A G PAICS Ensembl:ENSG00000128050 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs936431247 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7319650,Human_RBP_ID_26518376 Human_miRNA_ID_77261,Human_miRNA_ID_80430,Human_miRNA_ID_977028,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 48537 RMVar_ID_48537 Human_SNP_ID_184967152 A-to-I Human chr4 + 56459916 56459916 56459916 CAGACTTGCATTTTTTTTTTTTTTTTTGAGACAGGGTCTCACTGTCGCCCAGGCTGGAGTGCAGT CAGACTTGCATTTTTTTTTTTTTTTTTGAGACTGGGTCTCACTGTCGCCCAGGCTGGAGTGCAGT A T PAICS Ensembl:ENSG00000128050 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs936431247 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7319650,Human_RBP_ID_26518376 Human_miRNA_ID_77261,Human_miRNA_ID_80430,Human_miRNA_ID_977028,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 48538 RMVar_ID_48538 Human_SNP_ID_184967169 A-to-I Human chr4 + 56459960 56459959 56459961 TCGCCCAGGCTGGAGTGCAGTGGCGTGATCTCAGTTCACTGCTGCTTTCCCTCCTGGGCTCAAGC TCGCCCAGGCTGGAGTGCAGTGGCGTGATCTC__TTCACTGCTGCTTTCCCTCCTGGGCTCAAGC CAG C PAICS Ensembl:ENSG00000128050 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,31158229,32596459,32596459 RNA-Seq:(High) rs1191335125 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_622493,Human_RBP_ID_2853086,Human_RBP_ID_4787603,Human_RBP_ID_22826273,Human_RBP_ID_23191124,Human_RBP_ID_24501621,Human_RBP_ID_26516095 Human_miRNA_ID_827788,Human_miRNA_ID_2098677,Human_miRNA_ID_2104626,Human_miRNA_ID_2110579,Human_miRNA_ID_2163123,Human_miRNA_ID_2594342,Human_miRNA_ID_2737287,Human_miRNA_ID_3037890 RMVar_hsa_circ_226228,RMVar_hsa_circ_88685,RMVar_hsa_circ_88998,RMVar_hsa_circ_226231,RMVar_hsa_circ_87753,RMVar_hsa_circ_226233 48539 RMVar_ID_48539 Human_SNP_ID_184967170 A-to-I Human chr4 + 56459960 56459960 56459960 TCGCCCAGGCTGGAGTGCAGTGGCGTGATCTCAGTTCACTGCTGCTTTCCCTCCTGGGCTCAAGC TCGCCCAGGCTGGAGTGCAGTGGCGTGATCTCGGTTCACTGCTGCTTTCCCTCCTGGGCTCAAGC A G PAICS Ensembl:ENSG00000128050 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,31158229,32596459,32596459 RNA-Seq:(High) rs1431276325 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_622493,Human_RBP_ID_2853086,Human_RBP_ID_4787603,Human_RBP_ID_22826273,Human_RBP_ID_23191124,Human_RBP_ID_24501621,Human_RBP_ID_26516095 Human_miRNA_ID_827788,Human_miRNA_ID_2098677,Human_miRNA_ID_2104626,Human_miRNA_ID_2110579,Human_miRNA_ID_2163123,Human_miRNA_ID_2594342,Human_miRNA_ID_2737287,Human_miRNA_ID_3037890 RMVar_hsa_circ_226228,RMVar_hsa_circ_88685,RMVar_hsa_circ_88998,RMVar_hsa_circ_226231,RMVar_hsa_circ_87753,RMVar_hsa_circ_226233 48540 RMVar_ID_48540 Human_SNP_ID_184967179 A-to-I Human chr4 + 56459989 56459989 56459989 CTCAGTTCACTGCTGCTTTCCCTCCTGGGCTCAAGCAGTTCTCCCACCTCAGCCTCTCGACTAAC CTCAGTTCACTGCTGCTTTCCCTCCTGGGCTCGAGCAGTTCTCCCACCTCAGCCTCTCGACTAAC A G PAICS Ensembl:ENSG00000128050 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1428258208 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7319655,Human_RBP_ID_18027970,Human_RBP_ID_21056072,Human_RBP_ID_23191124,Human_RBP_ID_26518091 RMVar_hsa_circ_226228,RMVar_hsa_circ_88685,RMVar_hsa_circ_88998,RMVar_hsa_circ_226231,RMVar_hsa_circ_87753,RMVar_hsa_circ_226233 48541 RMVar_ID_48541 Human_SNP_ID_184967203 A-to-I Human chr4 + 56460096 56460096 56460096 TTTTGTAGAGATGAGCTCTCACTATGTCACCCAGGTTCGTCTCAAACTCCTGAACCCTAGTAATT TTTTGTAGAGATGAGCTCTCACTATGTCACCCGGGTTCGTCTCAAACTCCTGAACCCTAGTAATT A G PAICS Ensembl:ENSG00000128050 Protein coding 3'UTR GSE38233;GSE100210;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,temporal_cortex - 24183664,29129909,30559470 RNA-Seq:(High) rs1278444244 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_622495,Human_RBP_ID_7319660,Human_RBP_ID_15178848,Human_RBP_ID_17524545,Human_RBP_ID_17574769,Human_RBP_ID_18201929,Human_RBP_ID_18210208,Human_RBP_ID_26518094,Human_RBP_ID_27508715 RMVar_hsa_circ_226228,RMVar_hsa_circ_88685,RMVar_hsa_circ_88998,RMVar_hsa_circ_226231,RMVar_hsa_circ_87753,RMVar_hsa_circ_226233 48542 RMVar_ID_48542 Human_SNP_ID_184967208 A-to-I Human chr4 + 56460125 56460125 56460125 CCCAGGTTCGTCTCAAACTCCTGAACCCTAGTAATTCTCCTATCTCAGCCTCCCAAAGTGCTAGG CCCAGGTTCGTCTCAAACTCCTGAACCCTAGTGATTCTCCTATCTCAGCCTCCCAAAGTGCTAGG A G PAICS Ensembl:ENSG00000128050 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1133207 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_622495,Human_RBP_ID_8265833,Human_RBP_ID_15178848,Human_RBP_ID_17524545,Human_RBP_ID_17574769,Human_RBP_ID_22458608,Human_RBP_ID_23191127,Human_RBP_ID_26516099,Human_RBP_ID_27508715 RMVar_hsa_circ_226228,RMVar_hsa_circ_88685,RMVar_hsa_circ_88998,RMVar_hsa_circ_226231,RMVar_hsa_circ_87753,RMVar_hsa_circ_226233 48543 RMVar_ID_48543 Human_SNP_ID_184967210 A-to-I Human chr4 + 56460134 56460134 56460134 GTCTCAAACTCCTGAACCCTAGTAATTCTCCTATCTCAGCCTCCCAAAGTGCTAGGGTTACAGAC GTCTCAAACTCCTGAACCCTAGTAATTCTCCTGTCTCAGCCTCCCAAAGTGCTAGGGTTACAGAC A G PAICS Ensembl:ENSG00000128050 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041691767 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_622495,Human_RBP_ID_8265833,Human_RBP_ID_15178848,Human_RBP_ID_17524545,Human_RBP_ID_17575131,Human_RBP_ID_22458608,Human_RBP_ID_23191127,Human_RBP_ID_26516099,Human_RBP_ID_27508715 RMVar_hsa_circ_226228,RMVar_hsa_circ_88685,RMVar_hsa_circ_88998,RMVar_hsa_circ_226231,RMVar_hsa_circ_87753,RMVar_hsa_circ_226233 48544 RMVar_ID_48544 Human_SNP_ID_184967212 A-to-I Human chr4 + 56460147 56460147 56460147 GAACCCTAGTAATTCTCCTATCTCAGCCTCCCAAAGTGCTAGGGTTACAGACATGAGCCACTGTG GAACCCTAGTAATTCTCCTATCTCAGCCTCCCGAAGTGCTAGGGTTACAGACATGAGCCACTGTG A G PAICS Ensembl:ENSG00000128050 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,29129909,29129909,31158229,32596459 RNA-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 48545 RMVar_ID_48545 Human_SNP_ID_184967216 A-to-I Human chr4 + 56460155 56460155 56460155 GTAATTCTCCTATCTCAGCCTCCCAAAGTGCTAGGGTTACAGACATGAGCCACTGTGCCTGTCTA GTAATTCTCCTATCTCAGCCTCCCAAAGTGCTGGGGTTACAGACATGAGCCACTGTGCCTGTCTA A G PAICS Ensembl:ENSG00000128050 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1304661596 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_622496,Human_RBP_ID_1209030,Human_RBP_ID_4787612,Human_RBP_ID_8265833,Human_RBP_ID_17575131,Human_RBP_ID_22458608,Human_RBP_ID_23191127,Human_RBP_ID_26518095,Human_RBP_ID_27508718 Human_miRNA_ID_2227370,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 48546 RMVar_ID_48546 Human_SNP_ID_184967217 A-to-I Human chr4 + 56460167 56460167 56460167 TCTCAGCCTCCCAAAGTGCTAGGGTTACAGACATGAGCCACTGTGCCTGTCTAGACTTGTACTTT TCTCAGCCTCCCAAAGTGCTAGGGTTACAGACTTGAGCCACTGTGCCTGTCTAGACTTGTACTTT A T PAICS Ensembl:ENSG00000128050 Protein coding 3'UTR GSE38233;GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,32596459 RNA-Seq:(High) rs1479564774 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_622496,Human_RBP_ID_1209030,Human_RBP_ID_1317384,Human_RBP_ID_3741716,Human_RBP_ID_4787612,Human_RBP_ID_7319661,Human_RBP_ID_9161524,Human_RBP_ID_15178860,Human_RBP_ID_17575131,Human_RBP_ID_22458608,Human_RBP_ID_23191127,Human_RBP_ID_24059661,Human_RBP_ID_26518095 Human_miRNA_ID_1060577,Human_miRNA_ID_1994873,Human_miRNA_ID_2227370,Human_miRNA_ID_2503347,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 48547 RMVar_ID_48547 Human_SNP_ID_184967399 A-to-I Human chr4 + 56460856 56460856 56460856 AGCCAGCCGTGATGACAGGCACCTGTAATCCCAGCTACTCGGGAGGCTGAGGCATGAGAATTGCT AGCCAGCCGTGATGACAGGCACCTGTAATCCCGGCTACTCGGGAGGCTGAGGCATGAGAATTGCT A G PAICS Ensembl:ENSG00000128050 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs11549977 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4787643,Human_RBP_ID_17574770 Human_miRNA_ID_1359922 RMVar_hsa_circ_226228,RMVar_hsa_circ_88685,RMVar_hsa_circ_88998,RMVar_hsa_circ_226231,RMVar_hsa_circ_87753,RMVar_hsa_circ_226233 48548 RMVar_ID_48548 Human_SNP_ID_184967416 A-to-I Human chr4 + 56460916 56460916 56460916 TTGCTTGAACCCGGGAGGCGGAGGTTGCAGTGAGCCTAGATCATGCCACTGCACTCCAACCTGGG TTGCTTGAACCCGGGAGGCGGAGGTTGCAGTGGGCCTAGATCATGCCACTGCACTCCAACCTGGG A G PAICS Ensembl:ENSG00000128050 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,29129909,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs1415434741 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17574770 Human_miRNA_ID_678575 RMVar_hsa_circ_226228,RMVar_hsa_circ_88685,RMVar_hsa_circ_88998,RMVar_hsa_circ_226231,RMVar_hsa_circ_87753,RMVar_hsa_circ_226233 48549 RMVar_ID_48549 Human_SNP_ID_184967417 A-to-I Human chr4 + 56460921 56460921 56460921 TGAACCCGGGAGGCGGAGGTTGCAGTGAGCCTAGATCATGCCACTGCACTCCAACCTGGGCAGCA TGAACCCGGGAGGCGGAGGTTGCAGTGAGCCTGGATCATGCCACTGCACTCCAACCTGGGCAGCA A G PAICS Ensembl:ENSG00000128050 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1133213 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17574770 RMVar_hsa_circ_226228,RMVar_hsa_circ_88685,RMVar_hsa_circ_88998,RMVar_hsa_circ_226231,RMVar_hsa_circ_87753,RMVar_hsa_circ_226233 48550 RMVar_ID_48550 Human_SNP_ID_184967422 A-to-I Human chr4 + 56460950 56460950 56460950 CCTAGATCATGCCACTGCACTCCAACCTGGGCAGCAGAGCAAGACTCTGTCTCAAAAGGGGAAAA CCTAGATCATGCCACTGCACTCCAACCTGGGCGGCAGAGCAAGACTCTGTCTCAAAAGGGGAAAA A G PAICS Ensembl:ENSG00000128050 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs11549974 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17574770,Human_RBP_ID_26518099 Human_miRNA_ID_929099,Human_miRNA_ID_2394665,Human_miRNA_ID_2610875,Human_miRNA_ID_2906724,Human_miRNA_ID_3025555 RMVar_hsa_circ_226228,RMVar_hsa_circ_88685,RMVar_hsa_circ_88998,RMVar_hsa_circ_226231,RMVar_hsa_circ_87753,RMVar_hsa_circ_226233 48551 RMVar_ID_48551 Human_SNP_ID_184970554 A-to-I Human chr4 + 56472518 56472518 56472518 CAGGCATGTGCCAACTCGTGCAGCTAATTTTTATATTTTTTAGTAGAGATGGGGTTATGCCATGT CAGGCATGTGCCAACTCGTGCAGCTAATTTTTGTATTTTTTAGTAGAGATGGGGTTATGCCATGT A G SRP72 Ensembl:ENSG00000174780 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs770833207 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85906,RMVar_hsa_circ_3458,RMVar_hsa_circ_77557,RMVar_hsa_circ_226235,RMVar_hsa_circ_226236,RMVar_hsa_circ_47951,RMVar_hsa_circ_34292 48552 RMVar_ID_48552 Human_SNP_ID_184971221 A-to-I Human chr4 + 56474597 56474597 56474597 ACAGAATCTTACCCTGTTGCCCAGGCTGGAGTACAATGGCACGATCTCGGCTCACTGCAACCTCT ACAGAATCTTACCCTGTTGCCCAGGCTGGAGTGCAATGGCACGATCTCGGCTCACTGCAACCTCT A G SRP72 Ensembl:ENSG00000174780 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232435207 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85906,RMVar_hsa_circ_829,RMVar_hsa_circ_77557,RMVar_hsa_circ_226235,RMVar_hsa_circ_226236,RMVar_hsa_circ_62187,RMVar_hsa_circ_375097,RMVar_hsa_circ_120633,RMVar_hsa_circ_34887,RMVar_hsa_circ_83990,RMVar_hsa_circ_226239,RMVar_hsa_circ_226238,RMVar_hsa_circ_226241 48553 RMVar_ID_48553 Human_SNP_ID_184971504 A-to-I Human chr4 + 56475519 56475519 56475519 AGGAGGTTGAGGCTCCAGTGAGCTGAAATCATACCACTGTATTCCAGCCTGGGTGACAGAGTGAG AGGAGGTTGAGGCTCCAGTGAGCTGAAATCATGCCACTGTATTCCAGCCTGGGTGACAGAGTGAG A G SRP72 Ensembl:ENSG00000174780 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1196891313 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25835141 RMVar_hsa_circ_85906,RMVar_hsa_circ_829,RMVar_hsa_circ_77557,RMVar_hsa_circ_226235,RMVar_hsa_circ_226236,RMVar_hsa_circ_62187,RMVar_hsa_circ_375097,RMVar_hsa_circ_120633,RMVar_hsa_circ_34887,RMVar_hsa_circ_83990,RMVar_hsa_circ_226239,RMVar_hsa_circ_226238,RMVar_hsa_circ_226241 48554 RMVar_ID_48554 Human_SNP_ID_184976455 A-to-I Human chr4 + 56494503 56494503 56494503 CTCGCTCACTGCAGCCTCTGCCTCCCTGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGC CTCGCTCACTGCAGCCTCTGCCTCCCTGGTTCCAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGC A C SRP72 Ensembl:ENSG00000174780 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs964825792 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3380,RMVar_hsa_circ_120633,RMVar_hsa_circ_226238,RMVar_hsa_circ_376034,RMVar_hsa_circ_293133,RMVar_hsa_circ_226247,RMVar_hsa_circ_84973,RMVar_hsa_circ_226251 48555 RMVar_ID_48555 Human_SNP_ID_185085226 A-to-I Human chr4 + 56923401 56923401 56923401 GCCATCCTCTTGCCTCAGTCTCCTGAGTCGCTAGGTCTACTGGCACATGCCACCACTCCAGCTAA GCCATCCTCTTGCCTCAGTCTCCTGAGTCGCTTGGTCTACTGGCACATGCCACCACTCCAGCTAA A T REST Ensembl:ENSG00000084093 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1437336382 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15180110 48556 RMVar_ID_48556 Human_SNP_ID_185090069 A-to-I Human chr4 + 56939531 56939530 56939532 ACTTGAAAAAGATTATTATTTGTTTTTGAGACAGGGTCTCACCCTTTCACCCAGGCTGGAATGCA ACTTGAAAAAGATTATTATTTGTTTTTGAGAC__GGTCTCACCCTTTCACCCAGGCTGGAATGCA CAG C REST Ensembl:ENSG00000084093 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs919672970 Functional Loss DEL dbSNP153 33..34 33 - - - 48557 RMVar_ID_48557 Human_SNP_ID_185096502 A-to-I Human chr4 - 56963235 56963235 56963235 TTGGCTCACTGTAACCTCTACCTCCCAGGTTCAAGCAATCCTCCTGCCTCAGCCCCCCAGTAGCT TTGGCTCACTGTAACCTCTACCTCCCAGGTTCGAGCAATCCTCCTGCCTCAGCCCCCCAGTAGCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893152002 Functional Loss SNV dbSNP153 33..33 33 - - - 48558 RMVar_ID_48558 Human_SNP_ID_185097598 A-to-I Human chr4 - 56967137 56967137 56967137 GCTCAAGGGATTCACCCACCTCGGCCTTCCAAAATGCTGGGATTATAGGCATGAGCCACCACACC GCTCAAGGGATTCACCCACCTCGGCCTTCCAATATGCTGGGATTATAGGCATGAGCCACCACACC T A NOA1 Ensembl:ENSG00000084092 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1329400386 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103012,RMVar_hsa_circ_226260,RMVar_hsa_circ_86797,RMVar_hsa_circ_226259,RMVar_hsa_circ_346465,RMVar_hsa_circ_300900,RMVar_hsa_circ_226262,RMVar_hsa_circ_326219 48559 RMVar_ID_48559 Human_SNP_ID_185097614 A-to-I Human chr4 - 56967208 56967207 56967208 ACCCAGCTAATTTTTGTATTTTTTATAGAGACAGGGTTTTGCCATGTTTCCCAGGCTGGTCTCAA ACCCAGCTAATTTTTGTATTTTTTATAGAGAC_GGGTTTTGCCATGTTTCCCAGGCTGGTCTCAA CT C NOA1 Ensembl:ENSG00000084092 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1468635359 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_103012,RMVar_hsa_circ_226260,RMVar_hsa_circ_86797,RMVar_hsa_circ_226259,RMVar_hsa_circ_346465,RMVar_hsa_circ_300900,RMVar_hsa_circ_226262,RMVar_hsa_circ_326219 48560 RMVar_ID_48560 Human_SNP_ID_185097624 A-to-I Human chr4 - 56967258 56967258 56967258 ATCCCACCCCAGCCCCGCAAGTAGTCGGGACTACAGGCACACATCACCACACCCAGCTAATTTTT ATCCCACCCCAGCCCCGCAAGTAGTCGGGACTGCAGGCACACATCACCACACCCAGCTAATTTTT T C NOA1 Ensembl:ENSG00000084092 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs574744810 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103012,RMVar_hsa_circ_226260,RMVar_hsa_circ_86797,RMVar_hsa_circ_226259,RMVar_hsa_circ_346465,RMVar_hsa_circ_300900,RMVar_hsa_circ_226262,RMVar_hsa_circ_326219 48561 RMVar_ID_48561 Human_SNP_ID_185097642 A-to-I Human chr4 - 56967296 56967296 56967296 GGCTCACTGTGGCCTCAACCTCCTGGGCTCCAATGATCATCCCACCCCAGCCCCGCAAGTAGTCG GGCTCACTGTGGCCTCAACCTCCTGGGCTCCAGTGATCATCCCACCCCAGCCCCGCAAGTAGTCG T C NOA1 Ensembl:ENSG00000084092 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs571071925 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103012,RMVar_hsa_circ_226260,RMVar_hsa_circ_86797,RMVar_hsa_circ_226259,RMVar_hsa_circ_346465,RMVar_hsa_circ_300900,RMVar_hsa_circ_226262,RMVar_hsa_circ_326219 48562 RMVar_ID_48562 Human_SNP_ID_185097652 A-to-I Human chr4 - 56967336 56967329 56967337 TCTCTCTGTTGCCCAGACTGGAGTGCAGTGGTACAGTCACGGCTCACTGTGGCCTCAACCTCCTG TCTCTCTGTTGCCCAGACTGGAGTGCAGTGG________CGGCTCACTGTGGCCTCAACCTCCTG GTGACTGTA G NOA1 Ensembl:ENSG00000084092 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1183661033 Functional Loss DEL dbSNP153 32..39 33 - - - RMVar_hsa_circ_103012,RMVar_hsa_circ_226260,RMVar_hsa_circ_86797,RMVar_hsa_circ_226259,RMVar_hsa_circ_346465,RMVar_hsa_circ_300900,RMVar_hsa_circ_226262,RMVar_hsa_circ_326219 48563 RMVar_ID_48563 Human_SNP_ID_185098296 A-to-I Human chr4 - 56970197 56970197 56970197 CTGCCTCCCTGGCTCAAGCAATCCTCCACCTCAGCCTCCAGGGTAGCTGGGAACTACAGACACAC CTGCCTCCCTGGCTCAAGCAATCCTCCACCTCCGCCTCCAGGGTAGCTGGGAACTACAGACACAC T G NOA1 Ensembl:ENSG00000084092 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1395295238 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103012,RMVar_hsa_circ_226260,RMVar_hsa_circ_346465 48564 RMVar_ID_48564 Human_SNP_ID_185098297 A-to-I Human chr4 - 56970209 56970209 56970209 CCACTGTAACTTCTGCCTCCCTGGCTCAAGCAATCCTCCACCTCAGCCTCCAGGGTAGCTGGGAA CCACTGTAACTTCTGCCTCCCTGGCTCAAGCAGTCCTCCACCTCAGCCTCCAGGGTAGCTGGGAA T C NOA1 Ensembl:ENSG00000084092 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs549155553 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103012,RMVar_hsa_circ_226260,RMVar_hsa_circ_346465 48565 RMVar_ID_48565 Human_SNP_ID_185098350 A-to-I Human chr4 - 56970455 56970455 56970455 GTGAAACCCTGTCTCAACAAAAAAGAGAGACAAGGTTTCCCCTGTTGCCCAGGCTGGAATGCAGT GTGAAACCCTGTCTCAACAAAAAAGAGAGACAGGGTTTCCCCTGTTGCCCAGGCTGGAATGCAGT T C NOA1 Ensembl:ENSG00000084092 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs113869024 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103012,RMVar_hsa_circ_226260,RMVar_hsa_circ_346465 48566 RMVar_ID_48566 Human_SNP_ID_185098351 A-to-I Human chr4 - 56970458 56970457 56970459 AGAGTGAAACCCTGTCTCAACAAAAAAGAGAGACAAGGTTTCCCCTGTTGCCCAGGCTGGAATGC AGAGTGAAACCCTGTCTCAACAAAAAAGAGA__CAAGGTTTCCCCTGTTGCCCAGGCTGGAATGC GTC G NOA1 Ensembl:ENSG00000084092 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1206167098 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_103012,RMVar_hsa_circ_226260,RMVar_hsa_circ_346465 48567 RMVar_ID_48567 Human_SNP_ID_185098513 A-to-I Human chr4 - 56971130 56971130 56971130 TTTTGTATTTTTAATAGAGACAGGGTTTCGCCATGTTGGCCAGGCTGGTCTCAAACCCCTCACCT TTTTGTATTTTTAATAGAGACAGGGTTTCGCCGTGTTGGCCAGGCTGGTCTCAAACCCCTCACCT T C NOA1 Ensembl:ENSG00000084092 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs75202035 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103012,RMVar_hsa_circ_226260,RMVar_hsa_circ_346465 48568 RMVar_ID_48568 Human_SNP_ID_185098514 A-to-I Human chr4 - 56971130 56971130 56971130 TTTTGTATTTTTAATAGAGACAGGGTTTCGCCATGTTGGCCAGGCTGGTCTCAAACCCCTCACCT TTTTGTATTTTTAATAGAGACAGGGTTTCGCCCTGTTGGCCAGGCTGGTCTCAAACCCCTCACCT T G NOA1 Ensembl:ENSG00000084092 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs75202035 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103012,RMVar_hsa_circ_226260,RMVar_hsa_circ_346465 48569 RMVar_ID_48569 Human_SNP_ID_185099503 A-to-I Human chr4 - 56975187 56975187 56975187 GAAACCCTGTCTCTACTAAAGATACAAAAATTAGTCAGGCTGGTGGTGCGTGCCTGTAGTCCCAG GAAACCCTGTCTCTACTAAAGATACAAAAATTCGTCAGGCTGGTGGTGCGTGCCTGTAGTCCCAG T G NOA1 Ensembl:ENSG00000084092 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1227969158 Functional Loss SNV dbSNP153 33..33 33 - - - 48570 RMVar_ID_48570 Human_SNP_ID_185099577 A-to-I Human chr4 - 56975465 56975465 56975465 CACCATGCCCAGCTAATTTTTGTATCTTTGGTAGAGACAGGGTTTCAACATGTTGGCCAGGCAGG CACCATGCCCAGCTAATTTTTGTATCTTTGGTGGAGACAGGGTTTCAACATGTTGGCCAGGCAGG T C NOA1 Ensembl:ENSG00000084092 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1469246747 Functional Loss SNV dbSNP153 33..33 33 - - - 48571 RMVar_ID_48571 Human_SNP_ID_185100884 A-to-I Human chr4 + 56978789 56978786 56978790 AATTTACGCGTGTGCAACCCTAACCCCGGCCCAAGCTTGACCTACAATTTGCGCAGGCGCAGATC AATTTACGCGTGTGCAACCCTAACCCCGGC____GCTTGACCTACAATTTGCGCAGGCGCAGATC CCCAA C POLR2B Ensembl:ENSG00000047315 Protein coding 5'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1329041703 Functional Loss DEL dbSNP153 31..34 33 - - - RMVar_hsa_circ_14790,RMVar_hsa_circ_51731,RMVar_hsa_circ_18308,RMVar_hsa_circ_226264 48572 RMVar_ID_48572 Human_SNP_ID_185100885 A-to-I Human chr4 + 56978789 56978789 56978789 AATTTACGCGTGTGCAACCCTAACCCCGGCCCAAGCTTGACCTACAATTTGCGCAGGCGCAGATC AATTTACGCGTGTGCAACCCTAACCCCGGCCCGAGCTTGACCTACAATTTGCGCAGGCGCAGATC A G POLR2B Ensembl:ENSG00000047315 Protein coding 5'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs141351541 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14790,RMVar_hsa_circ_51731,RMVar_hsa_circ_18308,RMVar_hsa_circ_226264 48573 RMVar_ID_48573 Human_SNP_ID_185100891 A-to-I Human chr4 + 56978796 56978796 56978796 GCGTGTGCAACCCTAACCCCGGCCCAAGCTTGACCTACAATTTGCGCAGGCGCAGATCCTAACTT GCGTGTGCAACCCTAACCCCGGCCCAAGCTTGGCCTACAATTTGCGCAGGCGCAGATCCTAACTT A G POLR2B Ensembl:ENSG00000047315 Protein coding 5'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs974374263 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14790,RMVar_hsa_circ_51731,RMVar_hsa_circ_18308,RMVar_hsa_circ_226264 48574 RMVar_ID_48574 Human_SNP_ID_185101402 A-to-I Human chr4 + 56980597 56980597 56980597 GAAAAATTAGCTGGGCGTGGTCTTGCTCACCTATAGTCCCAGCTACTTGTGGGGCTGAGGCTGGA GAAAAATTAGCTGGGCGTGGTCTTGCTCACCTGTAGTCCCAGCTACTTGTGGGGCTGAGGCTGGA A G POLR2B Ensembl:ENSG00000047315 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs762391478 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14790,RMVar_hsa_circ_51731,RMVar_hsa_circ_18308,RMVar_hsa_circ_226264 48575 RMVar_ID_48575 Human_SNP_ID_185104037 A-to-I Human chr4 + 56991842 56991842 56991842 CCATGCTTGGCTAATTTTTTTGTATTTTTAGTAGAGATGGTGTTTCACATGTTGGCCAGGCCGAT CCATGCTTGGCTAATTTTTTTGTATTTTTAGTGGAGATGGTGTTTCACATGTTGGCCAGGCCGAT A G POLR2B Ensembl:ENSG00000047315 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1045843437 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14790,RMVar_hsa_circ_51731,RMVar_hsa_circ_326828,RMVar_hsa_circ_226265,RMVar_hsa_circ_371451,RMVar_hsa_circ_344862,RMVar_hsa_circ_378768,RMVar_hsa_circ_226266,RMVar_hsa_circ_226267 48576 RMVar_ID_48576 Human_SNP_ID_185104137 A-to-I Human chr4 + 56992276 56992276 56992276 CCTGAGCTCAAGAGTTTGAGACCAGCCTGGCCAATATGGTGAAACCCCGTCTCTACTAGTAAAGT CCTGAGCTCAAGAGTTTGAGACCAGCCTGGCCGATATGGTGAAACCCCGTCTCTACTAGTAAAGT A G POLR2B Ensembl:ENSG00000047315 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1301416256 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14790,RMVar_hsa_circ_51731,RMVar_hsa_circ_326828,RMVar_hsa_circ_226265,RMVar_hsa_circ_371451,RMVar_hsa_circ_344862,RMVar_hsa_circ_378768,RMVar_hsa_circ_226266,RMVar_hsa_circ_226267 48577 RMVar_ID_48577 Human_SNP_ID_185104178 A-to-I Human chr4 + 56992417 56992417 56992417 AACGTGGGAGACGGAGGTTGCAGCGAGCTGAGATCACGCCACTGCACTCCAGCCTGGGCGAGAGG AACGTGGGAGACGGAGGTTGCAGCGAGCTGAGTTCACGCCACTGCACTCCAGCCTGGGCGAGAGG A T POLR2B Ensembl:ENSG00000047315 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs147875380 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25835164 RMVar_hsa_circ_14790,RMVar_hsa_circ_51731,RMVar_hsa_circ_326828,RMVar_hsa_circ_226265,RMVar_hsa_circ_371451,RMVar_hsa_circ_344862,RMVar_hsa_circ_378768,RMVar_hsa_circ_226266,RMVar_hsa_circ_226267 48578 RMVar_ID_48578 Human_SNP_ID_185104415 A-to-I Human chr4 + 56993079 56993079 56993079 TAATCCCAGCACTTTGGGAGGCCTAGGCAGGCAGATCTCTTGAGGCCAGGAGTTTGAGACCATCC TAATCCCAGCACTTTGGGAGGCCTAGGCAGGCGGATCTCTTGAGGCCAGGAGTTTGAGACCATCC A G POLR2B Ensembl:ENSG00000047315 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1212442952 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14790,RMVar_hsa_circ_51731,RMVar_hsa_circ_326828,RMVar_hsa_circ_226265,RMVar_hsa_circ_371451,RMVar_hsa_circ_344862,RMVar_hsa_circ_378768,RMVar_hsa_circ_226266,RMVar_hsa_circ_226267 48579 RMVar_ID_48579 Human_SNP_ID_185106233 A-to-I Human chr4 + 57000178 57000178 57000178 TACAAAAAGGCCAGTCATGGTGATTCACGCCTATAATCTCAGCACTTTGGGAGGCCAGGGCGGGA TACAAAAAGGCCAGTCATGGTGATTCACGCCTGTAATCTCAGCACTTTGGGAGGCCAGGGCGGGA A G POLR2B Ensembl:ENSG00000047315 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1237249159 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14790,RMVar_hsa_circ_344862,RMVar_hsa_circ_226267,RMVar_hsa_circ_28846,RMVar_hsa_circ_36380 48580 RMVar_ID_48580 Human_SNP_ID_185106944 A-to-I Human chr4 + 57003268 57003268 57003268 CCTGGCCAACGTAGTGAAACCCTGTGTCTACTAAAAATACAAAAATTAGCTGGGCATGGTGGTGT CCTGGCCAACGTAGTGAAACCCTGTGTCTACTGAAAATACAAAAATTAGCTGGGCATGGTGGTGT A G POLR2B Ensembl:ENSG00000047315 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs920932112 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14790,RMVar_hsa_circ_344862,RMVar_hsa_circ_226267,RMVar_hsa_circ_28846,RMVar_hsa_circ_36380 48581 RMVar_ID_48581 Human_SNP_ID_185107058 A-to-I Human chr4 + 57003787 57003787 57003787 ATCACTGGAACCCAGGAGGCAGATGTTGTAGTAAGCCAAGATGGTGCCATTGCACTCCAGCCTGG ATCACTGGAACCCAGGAGGCAGATGTTGTAGTGAGCCAAGATGGTGCCATTGCACTCCAGCCTGG A G POLR2B Ensembl:ENSG00000047315 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1471499148 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14790,RMVar_hsa_circ_344862,RMVar_hsa_circ_226267,RMVar_hsa_circ_28846,RMVar_hsa_circ_36380 48582 RMVar_ID_48582 Human_SNP_ID_185107921 A-to-I Human chr4 + 57007223 57007223 57007223 CCTGAGGTCAGGAGTTTGAGACCAACCTGGCCAACATGGCGAAACCCCATCTCTATTAAAGATAC CCTGAGGTCAGGAGTTTGAGACCAACCTGGCCCACATGGCGAAACCCCATCTCTATTAAAGATAC A C POLR2B Ensembl:ENSG00000047315 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1212705990 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3913,RMVar_hsa_circ_28846,RMVar_hsa_circ_37384,RMVar_hsa_circ_348218,RMVar_hsa_circ_15248,RMVar_hsa_circ_10861,RMVar_hsa_circ_226270,RMVar_hsa_circ_73865,RMVar_hsa_circ_226271 48583 RMVar_ID_48583 Human_SNP_ID_185107927 A-to-I Human chr4 + 57007239 57007239 57007239 TGAGACCAACCTGGCCAACATGGCGAAACCCCATCTCTATTAAAGATACAAAAATTAGCTGGGCA TGAGACCAACCTGGCCAACATGGCGAAACCCCCTCTCTATTAAAGATACAAAAATTAGCTGGGCA A C POLR2B Ensembl:ENSG00000047315 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs980403289 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3913,RMVar_hsa_circ_28846,RMVar_hsa_circ_37384,RMVar_hsa_circ_348218,RMVar_hsa_circ_15248,RMVar_hsa_circ_10861,RMVar_hsa_circ_226270,RMVar_hsa_circ_73865,RMVar_hsa_circ_226271 48584 RMVar_ID_48584 Human_SNP_ID_185108164 A-to-I Human chr4 + 57008332 57008332 57008332 TTACACCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCCGCCACCACGCCTG TTACACCATTCTCCTGCCTCAGCCTCCCGAGTGGCTGGGACTACAGGCGCCCGCCACCACGCCTG A G POLR2B Ensembl:ENSG00000047315 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1292165399 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3913,RMVar_hsa_circ_28846,RMVar_hsa_circ_37384,RMVar_hsa_circ_348218,RMVar_hsa_circ_15248,RMVar_hsa_circ_10861,RMVar_hsa_circ_226270,RMVar_hsa_circ_73865,RMVar_hsa_circ_226271 48585 RMVar_ID_48585 Human_SNP_ID_185108831 A-to-I Human chr4 + 57011341 57011341 57011341 CCTGAGGTCAGGAGTTCAAGCGCAGCCTGGCCAATATGGCGAAACCCCATCTCTACTAAAAATAC CCTGAGGTCAGGAGTTCAAGCGCAGCCTGGCCGATATGGCGAAACCCCATCTCTACTAAAAATAC A G POLR2B Ensembl:ENSG00000047315 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1210077240 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3913,RMVar_hsa_circ_28846,RMVar_hsa_circ_37384,RMVar_hsa_circ_15248,RMVar_hsa_circ_10861,RMVar_hsa_circ_226270,RMVar_hsa_circ_26372,RMVar_hsa_circ_369152 48586 RMVar_ID_48586 Human_SNP_ID_185109161 A-to-I Human chr4 + 57012729 57012729 57012729 CTTTGTTGCCCAGGCTGGAGTAGAGTGTTGCTATCTTAGCTCACTGCAACCTCTGTCTCCCAGGT CTTTGTTGCCCAGGCTGGAGTAGAGTGTTGCTCTCTTAGCTCACTGCAACCTCTGTCTCCCAGGT A C POLR2B Ensembl:ENSG00000047315 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs985608584 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3913,RMVar_hsa_circ_28846,RMVar_hsa_circ_37384,RMVar_hsa_circ_15248,RMVar_hsa_circ_10861,RMVar_hsa_circ_226270,RMVar_hsa_circ_26372,RMVar_hsa_circ_369152 48587 RMVar_ID_48587 Human_SNP_ID_185109162 A-to-I Human chr4 + 57012729 57012729 57012729 CTTTGTTGCCCAGGCTGGAGTAGAGTGTTGCTATCTTAGCTCACTGCAACCTCTGTCTCCCAGGT CTTTGTTGCCCAGGCTGGAGTAGAGTGTTGCTGTCTTAGCTCACTGCAACCTCTGTCTCCCAGGT A G POLR2B Ensembl:ENSG00000047315 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs985608584 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3913,RMVar_hsa_circ_28846,RMVar_hsa_circ_37384,RMVar_hsa_circ_15248,RMVar_hsa_circ_10861,RMVar_hsa_circ_226270,RMVar_hsa_circ_26372,RMVar_hsa_circ_369152 48588 RMVar_ID_48588 Human_SNP_ID_185109167 A-to-I Human chr4 + 57012764 57012764 57012764 TTAGCTCACTGCAACCTCTGTCTCCCAGGTTCAAGAAATTCTCATGCCTCAGCCTCCTGAGTAGC TTAGCTCACTGCAACCTCTGTCTCCCAGGTTCCAGAAATTCTCATGCCTCAGCCTCCTGAGTAGC A C POLR2B Ensembl:ENSG00000047315 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1207108067 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3913,RMVar_hsa_circ_28846,RMVar_hsa_circ_37384,RMVar_hsa_circ_15248,RMVar_hsa_circ_10861,RMVar_hsa_circ_226270,RMVar_hsa_circ_26372,RMVar_hsa_circ_369152 48589 RMVar_ID_48589 Human_SNP_ID_185112330 A-to-I Human chr4 + 57025973 57025973 57025973 TTTTTTTTTGTAGAGGCTAGGCGCAATGGCTCATGTCTGCAATCCCAGCACTTTGGGAGGCCAAG TTTTTTTTTGTAGAGGCTAGGCGCAATGGCTCGTGTCTGCAATCCCAGCACTTTGGGAGGCCAAG A G POLR2B Ensembl:ENSG00000047315 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971689322 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10861,RMVar_hsa_circ_226277,RMVar_hsa_circ_76004 48590 RMVar_ID_48590 Human_SNP_ID_185114557 A-to-I Human chr4 - 57035581 57035580 57035581 TGGCACATGCCTGTAATCCCAGCTACTCGGGAAGCTGAGGCAGGAGAATCACTGGAATCCCGGAG TGGCACATGCCTGTAATCCCAGCTACTCGGGA_GCTGAGGCAGGAGAATCACTGGAATCCCGGAG CT C IGFBP7 Ensembl:ENSG00000163453 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417120737 Functional Loss DEL dbSNP153 33..33 33 - - - 48591 RMVar_ID_48591 Human_SNP_ID_185127493 A-to-I Human chr4 - 57088998 57088998 57088998 AGACAGAGTCTCACTCTGTTGCTCAGGCTGGAATGCAGTGGTGTGATCTCCACTCGCTGCCACCT AGACAGAGTCTCACTCTGTTGCTCAGGCTGGAGTGCAGTGGTGTGATCTCCACTCGCTGCCACCT T C IGFBP7 Ensembl:ENSG00000163453 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1430057846 Functional Loss SNV dbSNP153 33..33 33 - - - 48592 RMVar_ID_48592 Human_SNP_ID_185132181 A-to-I Human chr4 - 57110068 57110068 57110068 CATGGAGTGCGTGAAGAGCCGCAAGAGGCGGAAGGGTAAAGCCGGGGCAGCAGCCGGCGGTCCGG CATGGAGTGCGTGAAGAGCCGCAAGAGGCGGAGGGGTAAAGCCGGGGCAGCAGCCGGCGGTCCGG T C IGFBP7 Ensembl:ENSG00000163453 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1133243 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27508815 48593 RMVar_ID_48593 Human_SNP_ID_185132218 A-to-I Human chr4 - 57110120 57110120 57110120 AGGGCGAGCCGTGCGGGGGTGGCGGCGCCGGCAGGGGGTACTGCGCGCCGGGCATGGAGTGCGTG AGGGCGAGCCGTGCGGGGGTGGCGGCGCCGGCGGGGGGTACTGCGCGCCGGGCATGGAGTGCGTG T C IGFBP7 Ensembl:ENSG00000163453 Protein coding CDS GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 29129909,30559470 RNA-Seq:(High) rs11555284 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27508817 48594 RMVar_ID_48594 Human_SNP_ID_413917601 A-to-I Human chr9 - 120484608 120484608 120484608 GTGATTCTCCCACCCCAGCCTCCCAAGTATCTAGGATTCTACGCATGTGCCACCATGCCTGGCTA GTGATTCTCCCACCCCAGCCTCCCAAGTATCTGGGATTCTACGCATGTGCCACCATGCCTGGCTA T C CDK5RAP2 Ensembl:ENSG00000136861 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1052403355 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69233,RMVar_hsa_circ_58184,RMVar_hsa_circ_4108,RMVar_hsa_circ_1987,RMVar_hsa_circ_10527,RMVar_hsa_circ_315748,RMVar_hsa_circ_48901,RMVar_hsa_circ_259097,RMVar_hsa_circ_2455,RMVar_hsa_circ_24488,RMVar_hsa_circ_18907,RMVar_hsa_circ_13815,RMVar_hsa_circ_354587,RMVar_hsa_circ_362047,RMVar_hsa_circ_45160,RMVar_hsa_circ_56473,RMVar_hsa_circ_322467,RMVar_hsa_circ_61186,RMVar_hsa_circ_16854,RMVar_hsa_circ_278685,RMVar_hsa_circ_320524,RMVar_hsa_circ_364131,RMVar_hsa_circ_58098,RMVar_hsa_circ_64689,RMVar_hsa_circ_259100,RMVar_hsa_circ_259101,RMVar_hsa_circ_277224,RMVar_hsa_circ_338051,RMVar_hsa_circ_356030,RMVar_hsa_circ_362671,RMVar_hsa_circ_367036,RMVar_hsa_circ_355424,RMVar_hsa_circ_335551,RMVar_hsa_circ_72530,RMVar_hsa_circ_74482,RMVar_hsa_circ_64001,RMVar_hsa_circ_259102,RMVar_hsa_circ_259103 48595 RMVar_ID_48595 Human_SNP_ID_413931377 A-to-I Human chr9 - 120541290 120541290 120541290 CCTCTTGACAATGTATGTGATTTAGACAGCAAAACAGAAAGGTTAGATCTGGGCTGATAGGAGGG CCTCTTGACAATGTATGTGATTTAGACAGCAACACAGAAAGGTTAGATCTGGGCTGATAGGAGGG T G CDK5RAP2 Ensembl:ENSG00000136861 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1467445487 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1987,RMVar_hsa_circ_48901,RMVar_hsa_circ_2455,RMVar_hsa_circ_18907,RMVar_hsa_circ_56473,RMVar_hsa_circ_16854,RMVar_hsa_circ_58098,RMVar_hsa_circ_362671,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_71658,RMVar_hsa_circ_60200,RMVar_hsa_circ_354900,RMVar_hsa_circ_356464,RMVar_hsa_circ_362128,RMVar_hsa_circ_351040,RMVar_hsa_circ_73595,RMVar_hsa_circ_360298,RMVar_hsa_circ_62508,RMVar_hsa_circ_360978,RMVar_hsa_circ_320799,RMVar_hsa_circ_59752,RMVar_hsa_circ_259109,RMVar_hsa_circ_317762,RMVar_hsa_circ_359140 48596 RMVar_ID_48596 Human_SNP_ID_413951646 A-to-I Human chr9 - 120625498 120625498 120625498 ACAGAGTCTCCCTGTGTCGCCCAGGCTGGAGTACAGTGGCTATTCACAGGCCCGATCATGGCACA ACAGAGTCTCCCTGTGTCGCCCAGGCTGGAGTCCAGTGGCTATTCACAGGCCCGATCATGGCACA T G MEGF9 Ensembl:ENSG00000106780 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946103946 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_65987 48597 RMVar_ID_48597 Human_SNP_ID_413963381 A-to-I Human chr9 - 120676213 120676213 120676213 GCCATGTTGCCCAGGCTGAACTTGTGGACTCAAGTGATCTGTCTGCCTTGGCCTCCCAAAGTGCT GCCATGTTGCCCAGGCTGAACTTGTGGACTCATGTGATCTGTCTGCCTTGGCCTCCCAAAGTGCT T A MEGF9 Ensembl:ENSG00000106780 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1227013437 Functional Loss SNV dbSNP153 33..33 33 - - - 48598 RMVar_ID_48598 Human_SNP_ID_413982838 A-to-I Human chr9 - 120759545 120759545 120759545 CAGGTTGAAGAGATAGTTCTGTCAGCAATCCAACATCTATAGCAATGTGGAAAAAGTAATCAACT CAGGTTGAAGAGATAGTTCTGTCAGCAATCCAGCATCTATAGCAATGTGGAAAAAGTAATCAACT T C FBXW2 Ensembl:ENSG00000119402 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs566342443 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1057669,Human_RBP_ID_7892291,Human_RBP_ID_8924883,Human_RBP_ID_9314294,Human_RBP_ID_10415206,Human_RBP_ID_17435290,Human_RBP_ID_18902811,Human_RBP_ID_24281969,Human_RBP_ID_27782427 48599 RMVar_ID_48599 Human_SNP_ID_413986413 A-to-I Human chr9 - 120774460 120774460 120774460 TTGCCCAGGCTGGAATGCCGTGTCATGATCATAGCTCTCTGCAACTTTGAATCCCCAGGCTTAAG TTGCCCAGGCTGGAATGCCGTGTCATGATCATCGCTCTCTGCAACTTTGAATCCCCAGGCTTAAG T G FBXW2 Ensembl:ENSG00000119402 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1020313514 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16553534 RMVar_hsa_circ_26454,RMVar_hsa_circ_321624,RMVar_hsa_circ_358380,RMVar_hsa_circ_337717,RMVar_hsa_circ_259117 48600 RMVar_ID_48600 Human_SNP_ID_413988953 A-to-I Human chr9 - 120784487 120784487 120784487 ATGTCAGCCTCCCGGGTTTAGCTGGGACTACAAGCGAGCAACCCTATGCCTGGATCCTTTTTGTA ATGTCAGCCTCCCGGGTTTAGCTGGGACTACAGGCGAGCAACCCTATGCCTGGATCCTTTTTGTA T C FBXW2 Ensembl:ENSG00000119402 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1333641140 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_358380,RMVar_hsa_circ_117191,RMVar_hsa_circ_99931,RMVar_hsa_circ_259119,RMVar_hsa_circ_259120 48601 RMVar_ID_48601 Human_SNP_ID_413988973 A-to-I Human chr9 - 120784575 120784575 120784575 CCTCTCACTGGGTAGCTCCATCCTGGAGTGCAATGATGTGATCTTGGCTTTCTTCAACCTCCACC CCTCTCACTGGGTAGCTCCATCCTGGAGTGCAGTGATGTGATCTTGGCTTTCTTCAACCTCCACC T C FBXW2 Ensembl:ENSG00000119402 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1307406400 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16553943 RMVar_hsa_circ_358380,RMVar_hsa_circ_117191,RMVar_hsa_circ_99931,RMVar_hsa_circ_259119,RMVar_hsa_circ_259120 48602 RMVar_ID_48602 Human_SNP_ID_413989665 A-to-I Human chr9 - 120787169 120787169 120787169 GAAAAAGTAGCCGGGCGTGGCGGCATGCGCCTATAATCCCAGCTACTCGGGAGGCTGAAACAGGA GAAAAAGTAGCCGGGCGTGGCGGCATGCGCCTGTAATCCCAGCTACTCGGGAGGCTGAAACAGGA T C FBXW2 Ensembl:ENSG00000119402 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1344621656 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_358380,RMVar_hsa_circ_117191,RMVar_hsa_circ_99931,RMVar_hsa_circ_259119,RMVar_hsa_circ_259120 48603 RMVar_ID_48603 Human_SNP_ID_413989691 A-to-I Human chr9 - 120787230 120787230 120787230 GAGCTCAGGAGTTCGAGACCAGACTGGTCAACATGGTGAAATCCCGTCTCTACTGAAATACGAAA GAGCTCAGGAGTTCGAGACCAGACTGGTCAACGTGGTGAAATCCCGTCTCTACTGAAATACGAAA T C FBXW2 Ensembl:ENSG00000119402 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1213610143 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16554011,Human_RBP_ID_26199659 RMVar_hsa_circ_358380,RMVar_hsa_circ_117191,RMVar_hsa_circ_99931,RMVar_hsa_circ_259119,RMVar_hsa_circ_259120 48604 RMVar_ID_48604 Human_SNP_ID_413989707 A-to-I Human chr9 - 120787318 120787318 120787318 ATCTTTAAAATATGGGAAAGGAGGTCGGGCGCAGTGGCTCATGCCTGTAATTCTAGCACTTTGGG ATCTTTAAAATATGGGAAAGGAGGTCGGGCGCGGTGGCTCATGCCTGTAATTCTAGCACTTTGGG T C FBXW2 Ensembl:ENSG00000119402 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs898873300 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_358380,RMVar_hsa_circ_117191,RMVar_hsa_circ_99931,RMVar_hsa_circ_259119,RMVar_hsa_circ_259120 48605 RMVar_ID_48605 Human_SNP_ID_413989708 A-to-I Human chr9 - 120787318 120787318 120787318 ATCTTTAAAATATGGGAAAGGAGGTCGGGCGCAGTGGCTCATGCCTGTAATTCTAGCACTTTGGG ATCTTTAAAATATGGGAAAGGAGGTCGGGCGCCGTGGCTCATGCCTGTAATTCTAGCACTTTGGG T G FBXW2 Ensembl:ENSG00000119402 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs898873300 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_358380,RMVar_hsa_circ_117191,RMVar_hsa_circ_99931,RMVar_hsa_circ_259119,RMVar_hsa_circ_259120 48606 RMVar_ID_48606 Human_SNP_ID_413996849 A-to-I Human chr9 - 120817546 120817546 120817546 TGCTTCAGGGCTGGGCGCGGTGGCTAACACCTATAATTCCCAGCACTTTGGGAGGCCAAGATGGG TGCTTCAGGGCTGGGCGCGGTGGCTAACACCTGTAATTCCCAGCACTTTGGGAGGCCAAGATGGG T C PSMD5 Ensembl:ENSG00000095261 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1439129521 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8224612,Human_RBP_ID_17437330 RMVar_hsa_circ_95116,RMVar_hsa_circ_259125,RMVar_hsa_circ_90631,RMVar_hsa_circ_259124 48607 RMVar_ID_48607 Human_SNP_ID_414002095 A-to-I Human chr9 - 120839929 120839925 120839929 TTTAATAGAGATGCAGTTTCACCATGTTGGCCAGGCTGGTGTCGAACTCCTGACCTCAAGTGATC TTTAATAGAGATGCAGTTTCACCATGTTGGCC____TGGTGTCGAACTCCTGACCTCAAGTGATC AGCCT A PSMD5 Ensembl:ENSG00000095261 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1466260600 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_90631,RMVar_hsa_circ_259124,RMVar_hsa_circ_127217,RMVar_hsa_circ_259136 48608 RMVar_ID_48608 Human_SNP_ID_414016911 A-to-I Human chr9 - 120897722 120897722 120897722 CGCCTGCCTCGGCCTGCCAAGCTGCTGGGATTACAGGTGTGAGCCACCATGCCCGGCTGAGAATT CGCCTGCCTCGGCCTGCCAAGCTGCTGGGATTGCAGGTGTGAGCCACCATGCCCGGCTGAGAATT T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1163931164 Functional Loss SNV dbSNP153 33..33 33 - - - 48609 RMVar_ID_48609 Human_SNP_ID_414016915 A-to-I Human chr9 - 120897735 120897735 120897735 ACCTCAAGTGATCCGCCTGCCTCGGCCTGCCAAGCTGCTGGGATTACAGGTGTGAGCCACCATGC ACCTCAAGTGATCCGCCTGCCTCGGCCTGCCAGGCTGCTGGGATTACAGGTGTGAGCCACCATGC T C - - Other Unknown GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1447070487 Functional Loss SNV dbSNP153 33..33 33 - - - 48610 RMVar_ID_48610 Human_SNP_ID_414016927 A-to-I Human chr9 - 120897761 120897761 120897761 TTGGCCAGACTGGTCTCGAAATCCTGACCTCAAGTGATCCGCCTGCCTCGGCCTGCCAAGCTGCT TTGGCCAGACTGGTCTCGAAATCCTGACCTCATGTGATCCGCCTGCCTCGGCCTGCCAAGCTGCT T A - - Other Unknown GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1444442814 Functional Loss SNV dbSNP153 33..33 33 - - - 48611 RMVar_ID_48611 Human_SNP_ID_414016928 A-to-I Human chr9 - 120897762 120897762 120897762 GTTGGCCAGACTGGTCTCGAAATCCTGACCTCAAGTGATCCGCCTGCCTCGGCCTGCCAAGCTGC GTTGGCCAGACTGGTCTCGAAATCCTGACCTCGAGTGATCCGCCTGCCTCGGCCTGCCAAGCTGC T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs923624340 Functional Loss SNV dbSNP153 33..33 33 - - - 48612 RMVar_ID_48612 Human_SNP_ID_414016938 A-to-I Human chr9 - 120897799 120897799 120897799 CATTTTTTGTATTTTTGCAGAGATGGGGTTTCACCACGTTGGCCAGACTGGTCTCGAAATCCTGA CATTTTTTGTATTTTTGCAGAGATGGGGTTTCGCCACGTTGGCCAGACTGGTCTCGAAATCCTGA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1475665223 Functional Loss SNV dbSNP153 33..33 33 - - - 48613 RMVar_ID_48613 Human_SNP_ID_414016944 A-to-I Human chr9 - 120897821 120897821 120897821 GGGCCCACCACCACACCCGGCTCATTTTTTGTATTTTTGCAGAGATGGGGTTTCACCACGTTGGC GGGCCCACCACCACACCCGGCTCATTTTTTGTGTTTTTGCAGAGATGGGGTTTCACCACGTTGGC T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1223762743 Functional Loss SNV dbSNP153 33..33 33 - - - 48614 RMVar_ID_48614 Human_SNP_ID_414017620 A-to-I Human chr9 - 120900793 120900793 120900793 GGAAGCCAAGGCAGGAGGATTGCTTGAGGCCAAGAATTTAAGACCAGCCTGGGCAACATAGCAAG GGAAGCCAAGGCAGGAGGATTGCTTGAGGCCAGGAATTTAAGACCAGCCTGGGCAACATAGCAAG T C - - Other Unknown GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1263045222 Functional Loss SNV dbSNP153 33..33 33 - - - 48615 RMVar_ID_48615 Human_SNP_ID_414017791 A-to-I Human chr9 - 120901467 120901467 120901467 TTTGCAGCTGGGTGTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAAGCCAAGGCGGGTGGA TTTGCAGCTGGGTGTGGTGGCTCACACCTGTAGTCCCAGCACTTTGGGAAGCCAAGGCGGGTGGA T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1456388155 Functional Loss SNV dbSNP153 33..33 33 - - - 48616 RMVar_ID_48616 Human_SNP_ID_414017792 A-to-I Human chr9 - 120901467 120901467 120901467 TTTGCAGCTGGGTGTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAAGCCAAGGCGGGTGGA TTTGCAGCTGGGTGTGGTGGCTCACACCTGTACTCCCAGCACTTTGGGAAGCCAAGGCGGGTGGA T G - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1456388155 Functional Loss SNV dbSNP153 33..33 33 - - - 48617 RMVar_ID_48617 Human_SNP_ID_414061633 A-to-I Human chr9 + 121092282 121092282 121092282 AATGCAAGGCACCAACAGGGCAGATTTTGCCCATTGTGTTCACTACTCTAGCATTACTGCCTGGT AATGCAAGGCACCAACAGGGCAGATTTTGCCCGTTGTGTTCACTACTCTAGCATTACTGCCTGGT A G CNTRL Ensembl:ENSG00000119397 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1055402774 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16033,RMVar_hsa_circ_333337,RMVar_hsa_circ_21423,RMVar_hsa_circ_359356,RMVar_hsa_circ_311979,RMVar_hsa_circ_316719,RMVar_hsa_circ_60198,RMVar_hsa_circ_112631,RMVar_hsa_circ_259168,RMVar_hsa_circ_259169,RMVar_hsa_circ_259167,RMVar_hsa_circ_38071,RMVar_hsa_circ_259170 48618 RMVar_ID_48618 Human_SNP_ID_414080875 A-to-I Human chr9 + 121170213 121170213 121170213 GTCTCCCATGCTAGATTGAGTGGCGCAATCTCAGCTCACTGCAGCCTCTGCTTCCTGGGTTCAAG GTCTCCCATGCTAGATTGAGTGGCGCAATCTCGGCTCACTGCAGCCTCTGCTTCCTGGGTTCAAG A G CNTRL Ensembl:ENSG00000119397 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1246206007 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3836,RMVar_hsa_circ_112631,RMVar_hsa_circ_259170,RMVar_hsa_circ_89896,RMVar_hsa_circ_259171,RMVar_hsa_circ_49387,RMVar_hsa_circ_19385,RMVar_hsa_circ_52388,RMVar_hsa_circ_28986,RMVar_hsa_circ_322228,RMVar_hsa_circ_265828,RMVar_hsa_circ_11627,RMVar_hsa_circ_45324,RMVar_hsa_circ_259186,RMVar_hsa_circ_351815,RMVar_hsa_circ_259190,RMVar_hsa_circ_297226,RMVar_hsa_circ_259193 48619 RMVar_ID_48619 Human_SNP_ID_414081437 A-to-I Human chr9 + 121172520 121172520 121172520 AAAAGTAGCTAGGTGTGGTGGTGTACACCTGTAGTCCCAGCTATTCGGGAGGCTGAGGGGGGAGG AAAAGTAGCTAGGTGTGGTGGTGTACACCTGTGGTCCCAGCTATTCGGGAGGCTGAGGGGGGAGG A G CNTRL Ensembl:ENSG00000119397 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1195763574 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3836,RMVar_hsa_circ_112631,RMVar_hsa_circ_259170,RMVar_hsa_circ_89896,RMVar_hsa_circ_259171,RMVar_hsa_circ_49387,RMVar_hsa_circ_19385,RMVar_hsa_circ_45324,RMVar_hsa_circ_259186,RMVar_hsa_circ_297226,RMVar_hsa_circ_36013,RMVar_hsa_circ_259193,RMVar_hsa_circ_259195 48620 RMVar_ID_48620 Human_SNP_ID_414108468 A-to-I Human chr9 + 121290911 121290911 121290911 ATTGTCCAGGTTGGTCTTGAACTCTGGGGCTCAAGTGATCCTCCCTCCTCAGCCTCCCAAAGTGC ATTGTCCAGGTTGGTCTTGAACTCTGGGGCTCCAGTGATCCTCCCTCCTCAGCCTCCCAAAGTGC A C GSN Ensembl:ENSG00000148180 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs546095698 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49928 48621 RMVar_ID_48621 Human_SNP_ID_414108748 A-to-I Human chr9 + 121292086 121292086 121292086 GCCTGGCTAATTTTTTAATTTTGTGTAGAGACAGGGTCTCACTCTGTTTCCCAGGCTGTTCTCAA GCCTGGCTAATTTTTTAATTTTGTGTAGAGACGGGGTCTCACTCTGTTTCCCAGGCTGTTCTCAA A G GSN Ensembl:ENSG00000148180 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1287180946 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49928 48622 RMVar_ID_48622 Human_SNP_ID_414269709 A-to-I Human chr9 - 121950070 121950070 121950070 CAAGAACGTGACCTGATGCAAGCTTTGGGCACAAAGGGACCGAAATGGGAATGTGTCCTCCTTAG CAAGAACGTGACCTGATGCAAGCTTTGGGCACGAAGGGACCGAAATGGGAATGTGTCCTCCTTAG T C TTLL11-IT1,TTLL11 Ensembl:ENSG00000237548,Ensembl:ENSG00000175764 lincRNA,Protein coding intron,intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1352431284 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_286400,RMVar_hsa_circ_299839 48623 RMVar_ID_48623 Human_SNP_ID_414269710 A-to-I Human chr9 - 121950072 121950072 121950072 AGCAAGAACGTGACCTGATGCAAGCTTTGGGCACAAAGGGACCGAAATGGGAATGTGTCCTCCTT AGCAAGAACGTGACCTGATGCAAGCTTTGGGCGCAAAGGGACCGAAATGGGAATGTGTCCTCCTT T C TTLL11-IT1,TTLL11 Ensembl:ENSG00000237548,Ensembl:ENSG00000175764 lincRNA,Protein coding intron,intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs934735573 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_286400,RMVar_hsa_circ_299839 48624 RMVar_ID_48624 Human_SNP_ID_414342870 A-to-I Human chr9 - 122259969 122259969 122259969 CAAGGGGAGGCCGGGCACAGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGACGAGGCAGGC CAAGGGGAGGCCGGGCACAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGACGAGGCAGGC T C RBM18 Ensembl:ENSG00000119446 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1364775054 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_346402,RMVar_hsa_circ_329016 48625 RMVar_ID_48625 Human_SNP_ID_414342938 A-to-I Human chr9 - 122260224 122260224 122260224 CTCATGCCTCAGCCTCCCGAGTAGTTGGGACTACAGGCATGCGCCACCATGCTGGCTGATTTTTG CTCATGCCTCAGCCTCCCGAGTAGTTGGGACTGCAGGCATGCGCCACCATGCTGGCTGATTTTTG T C RBM18 Ensembl:ENSG00000119446 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1458744619 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_346402,RMVar_hsa_circ_329016 48626 RMVar_ID_48626 Human_SNP_ID_414344758 A-to-I Human chr9 + 122267566 122267566 122267566 GGCCTGAAGTGATCCTCCTTCCTTAGCATCCCAAGTAACTGGGACTATAGGCACCCATCACTGTT GGCCTGAAGTGATCCTCCTTCCTTAGCATCCCCAGTAACTGGGACTATAGGCACCCATCACTGTT A C MRRF Ensembl:ENSG00000148187 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1361741006 Functional Loss SNV dbSNP153 33..33 33 - - - 48627 RMVar_ID_48627 Human_SNP_ID_414358680 A-to-I Human chr9 + 122328162 122328162 122328162 CCTGGCTAACTTTTAAAATTATTTGTAGAGACAAGGTCTTGGCTATGTTGCCCAGGCTGATCTCA CCTGGCTAACTTTTAAAATTATTTGTAGAGACTAGGTCTTGGCTATGTTGCCCAGGCTGATCTCA A T MRRF Ensembl:ENSG00000148187 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968755095 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16556459 48628 RMVar_ID_48628 Human_SNP_ID_414359237 A-to-I Human chr9 + 122330661 122330661 122330661 TGTCCAGAGACACACAGAGGGCCTAGTGCAGTAGCTCATGCCTGGAATCTCAGCACTTTGGGTGG TGTCCAGAGACACACAGAGGGCCTAGTGCAGTTGCTCATGCCTGGAATCTCAGCACTTTGGGTGG A T MRRF Ensembl:ENSG00000148187 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs897998181 Functional Loss SNV dbSNP153 33..33 33 - - - 48629 RMVar_ID_48629 Human_SNP_ID_414373395 A-to-I Human chr9 + 122388630 122388630 122388630 CTGGGAAGCTCAGAGCAACAGATGGAGGCTAGAAGTCTGAATTCAAGGTGTCAGCAGTGCCATGT CTGGGAAGCTCAGAGCAACAGATGGAGGCTAGGAGTCTGAATTCAAGGTGTCAGCAGTGCCATGT A G PTGS1 Ensembl:ENSG00000095303 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1420163650 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44289 48630 RMVar_ID_48630 Human_SNP_ID_414383697 A-to-I Human chr9 + 122428346 122428346 122428346 CTGCTCGCTGCAGCCTCTGTCTCCCGGGTTCGAGTGATTCTCCTGCCTCAGCCTCGCGAGTAGTT CTGCTCGCTGCAGCCTCTGTCTCCCGGGTTCGGGTGATTCTCCTGCCTCAGCCTCGCGAGTAGTT A G AL359636.2 Ensembl:ENSG00000234156 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs544033409 Functional Loss SNV dbSNP153 33..33 33 - - - 48631 RMVar_ID_48631 Human_SNP_ID_414445695 A-to-I Human chr9 + 122686166 122686166 122686166 CCAGGTCCCTGATGAAACACACACCACCATCCAGGAGGCCCAGGGAAGGTGCAATGGATGAGCTT CCAGGTCCCTGATGAAACACACACCACCATCCGGGAGGCCCAGGGAAGGTGCAATGGATGAGCTT A G TLK1P1 Ensembl:ENSG00000226783 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910718494 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7952182 48632 RMVar_ID_48632 Human_SNP_ID_414478270 A-to-I Human chr9 - 122817679 122817679 122817679 ATTCCAGCACTTTGGGAGGCTGAGGCAGACATAGTGAGGCCTCATCTCTACAAAAAATAGAAAAA ATTCCAGCACTTTGGGAGGCTGAGGCAGACATGGTGAGGCCTCATCTCTACAAAAAATAGAAAAA T C PDCL Ensembl:ENSG00000136940 Protein coding intron GSE38233;GSE107867 cultured B-cells;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 24183664,30559470 RNA-Seq:(High) rs780787582 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26565229 48633 RMVar_ID_48633 Human_SNP_ID_414478925 A-to-I Human chr9 - 122820412 122820412 122820412 ATCATGGTTCATATTTATGAGGATGGCATTCCAGGGACCGAAGCCATGAATGGTTGCATGATCTG ATCATGGTTCATATTTATGAGGATGGCATTCCGGGGACCGAAGCCATGAATGGTTGCATGATCTG T C PDCL Ensembl:ENSG00000136940 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1330185267 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_710925,Human_RBP_ID_7893552,Human_RBP_ID_16556599,Human_RBP_ID_22776537 Human_miRNA_ID_259737,Human_miRNA_ID_263532 48634 RMVar_ID_48634 Human_SNP_ID_414480162 A-to-I Human chr9 - 122825326 122825326 122825326 GAAATCCCGTCTCTACTAAAATACAAAAAGTTAGCCAGGTGTGGGGGCATGCGGCTGTAGGCCCA GAAATCCCGTCTCTACTAAAATACAAAAAGTTCGCCAGGTGTGGGGGCATGCGGCTGTAGGCCCA T G PDCL Ensembl:ENSG00000136940 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs895056861 Functional Loss SNV dbSNP153 33..33 33 - - - 48635 RMVar_ID_48635 Human_SNP_ID_414484524 A-to-I Human chr9 - 122842355 122842355 122842355 CTGCCTCTACTAAAAATACAAAAAATTAGCCAAGCATGGTGGCAAGCACCTGTAGTTTCAGGAAC CTGCCTCTACTAAAAATACAAAAAATTAGCCACGCATGGTGGCAAGCACCTGTAGTTTCAGGAAC T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1222133934 Functional Loss SNV dbSNP153 33..33 33 - - - 48636 RMVar_ID_48636 Human_SNP_ID_414489909 A-to-I Human chr9 - 122861240 122861240 122861240 TTGATCTGCCTGCCTCGGCCTCCCAAAGTGCTAGGATTACAGGTGTGAGCCACCGTGCCCGGCCG TTGATCTGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGTGCCCGGCCG T C RC3H2 Ensembl:ENSG00000056586 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs561735913 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39276,RMVar_hsa_circ_303645,RMVar_hsa_circ_289440,RMVar_hsa_circ_259248,RMVar_hsa_circ_259249,RMVar_hsa_circ_259252,RMVar_hsa_circ_121785,RMVar_hsa_circ_359363,RMVar_hsa_circ_373815,RMVar_hsa_circ_363059,RMVar_hsa_circ_112021,RMVar_hsa_circ_11316,RMVar_hsa_circ_11405,RMVar_hsa_circ_259253,RMVar_hsa_circ_259254,RMVar_hsa_circ_259258,RMVar_hsa_circ_81323,RMVar_hsa_circ_62391,RMVar_hsa_circ_102313,RMVar_hsa_circ_100216,RMVar_hsa_circ_259260,RMVar_hsa_circ_325367,RMVar_hsa_circ_36093,RMVar_hsa_circ_259261,RMVar_hsa_circ_259262 48637 RMVar_ID_48637 Human_SNP_ID_414490340 A-to-I Human chr9 - 122862795 122862795 122862795 CACCTGCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTAAGTAGCTGGGATTACAGGCACCTG CACCTGCCAGGTTCAAGCAATTCTCCTGCCTCGGCCTCCTAAGTAGCTGGGATTACAGGCACCTG T C RC3H2 Ensembl:ENSG00000056586 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1479345708 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39276,RMVar_hsa_circ_303645,RMVar_hsa_circ_289440,RMVar_hsa_circ_259248,RMVar_hsa_circ_259249,RMVar_hsa_circ_259252,RMVar_hsa_circ_121785,RMVar_hsa_circ_359363,RMVar_hsa_circ_373815,RMVar_hsa_circ_363059,RMVar_hsa_circ_112021,RMVar_hsa_circ_11316,RMVar_hsa_circ_11405,RMVar_hsa_circ_259253,RMVar_hsa_circ_259254,RMVar_hsa_circ_259258,RMVar_hsa_circ_81323,RMVar_hsa_circ_62391,RMVar_hsa_circ_102313,RMVar_hsa_circ_100216,RMVar_hsa_circ_259260,RMVar_hsa_circ_325367,RMVar_hsa_circ_36093,RMVar_hsa_circ_259261,RMVar_hsa_circ_259262 48638 RMVar_ID_48638 Human_SNP_ID_414490342 A-to-I Human chr9 - 122862808 122862808 122862808 TCACTGCAACCTCCACCTGCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTAAGTAGCTGGGA TCACTGCAACCTCCACCTGCCAGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCTAAGTAGCTGGGA T C RC3H2 Ensembl:ENSG00000056586 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs199700970 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39276,RMVar_hsa_circ_303645,RMVar_hsa_circ_289440,RMVar_hsa_circ_259248,RMVar_hsa_circ_259249,RMVar_hsa_circ_259252,RMVar_hsa_circ_121785,RMVar_hsa_circ_359363,RMVar_hsa_circ_373815,RMVar_hsa_circ_363059,RMVar_hsa_circ_112021,RMVar_hsa_circ_11316,RMVar_hsa_circ_11405,RMVar_hsa_circ_259253,RMVar_hsa_circ_259254,RMVar_hsa_circ_259258,RMVar_hsa_circ_81323,RMVar_hsa_circ_62391,RMVar_hsa_circ_102313,RMVar_hsa_circ_100216,RMVar_hsa_circ_259260,RMVar_hsa_circ_325367,RMVar_hsa_circ_36093,RMVar_hsa_circ_259261,RMVar_hsa_circ_259262 48639 RMVar_ID_48639 Human_SNP_ID_414490658 A-to-I Human chr9 - 122864003 122864003 122864003 GCTGGGCACGGTGGCTCAGGCCTGTAATCCCAACACTTTGGGAGGCCGAGGTGGGCAGATCACCT GCTGGGCACGGTGGCTCAGGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGCAGATCACCT T C RC3H2 Ensembl:ENSG00000056586 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1201215750 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39276,RMVar_hsa_circ_303645,RMVar_hsa_circ_289440,RMVar_hsa_circ_259248,RMVar_hsa_circ_259249,RMVar_hsa_circ_259252,RMVar_hsa_circ_121785,RMVar_hsa_circ_359363,RMVar_hsa_circ_373815,RMVar_hsa_circ_363059,RMVar_hsa_circ_112021,RMVar_hsa_circ_11316,RMVar_hsa_circ_11405,RMVar_hsa_circ_259253,RMVar_hsa_circ_259254,RMVar_hsa_circ_259258,RMVar_hsa_circ_81323,RMVar_hsa_circ_62391,RMVar_hsa_circ_102313,RMVar_hsa_circ_100216,RMVar_hsa_circ_259260,RMVar_hsa_circ_325367,RMVar_hsa_circ_36093,RMVar_hsa_circ_259261,RMVar_hsa_circ_259262 48640 RMVar_ID_48640 Human_SNP_ID_414494856 A-to-I Human chr9 - 122877194 122877194 122877194 TGTGTGGCCCACAGTTGTGGTCCCAGCTGCTCAAAAGACTGAAGTGGAAGGATTGCTTGAACCCC TGTGTGGCCCACAGTTGTGGTCCCAGCTGCTCGAAAGACTGAAGTGGAAGGATTGCTTGAACCCC T C RC3H2 Ensembl:ENSG00000056586 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1310364081 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_289440,RMVar_hsa_circ_259249,RMVar_hsa_circ_359363,RMVar_hsa_circ_373815,RMVar_hsa_circ_363059,RMVar_hsa_circ_112021,RMVar_hsa_circ_11405,RMVar_hsa_circ_259253,RMVar_hsa_circ_259254,RMVar_hsa_circ_259258,RMVar_hsa_circ_81323,RMVar_hsa_circ_62391,RMVar_hsa_circ_102313,RMVar_hsa_circ_100216,RMVar_hsa_circ_259260,RMVar_hsa_circ_325367,RMVar_hsa_circ_36093,RMVar_hsa_circ_259266,RMVar_hsa_circ_282360,RMVar_hsa_circ_259261,RMVar_hsa_circ_259262,RMVar_hsa_circ_313705,RMVar_hsa_circ_342864,RMVar_hsa_circ_290783,RMVar_hsa_circ_71839,RMVar_hsa_circ_276714,RMVar_hsa_circ_259267,RMVar_hsa_circ_259264,RMVar_hsa_circ_259265,RMVar_hsa_circ_259263 48641 RMVar_ID_48641 Human_SNP_ID_414499051 A-to-I Human chr9 - 122893372 122893372 122893372 CTCCTGCCTCAGCCTCCTGAGTAGCTAGAATCACAGGCATCCACCACCACACCTGGCTAATTTTT CTCCTGCCTCAGCCTCCTGAGTAGCTAGAATCGCAGGCATCCACCACCACACCTGGCTAATTTTT T C RC3H2 Ensembl:ENSG00000056586 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1318141380 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_289440,RMVar_hsa_circ_259249,RMVar_hsa_circ_373815,RMVar_hsa_circ_11405,RMVar_hsa_circ_259253,RMVar_hsa_circ_62391,RMVar_hsa_circ_259277,RMVar_hsa_circ_276714,RMVar_hsa_circ_259263,RMVar_hsa_circ_276808,RMVar_hsa_circ_259272,RMVar_hsa_circ_259274,RMVar_hsa_circ_318079,RMVar_hsa_circ_377927,RMVar_hsa_circ_110472,RMVar_hsa_circ_343989,RMVar_hsa_circ_259275,RMVar_hsa_circ_259276,RMVar_hsa_circ_308030,RMVar_hsa_circ_292614,RMVar_hsa_circ_259281,RMVar_hsa_circ_259282,RMVar_hsa_circ_301048 48642 RMVar_ID_48642 Human_SNP_ID_414501497 A-to-I Human chr9 - 122902579 122902579 122902579 CCGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCACGCCTAGCCTCTTTTAACCTTTTTT CCGCCTCCCAAAGTGCTGGGATTACAGGCGTGCGCCACCACGCCTAGCCTCTTTTAACCTTTTTT T G RC3H2 Ensembl:ENSG00000056586 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs552892404 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110472,RMVar_hsa_circ_259276 48643 RMVar_ID_48643 Human_SNP_ID_414501521 A-to-I Human chr9 - 122902643 122902643 122902643 TTTGCCATGTTGACCAGGCTGGTCTGGAACTCATGACCTCAAGTGATCCACCCACCTCCCGCCTC TTTGCCATGTTGACCAGGCTGGTCTGGAACTCTTGACCTCAAGTGATCCACCCACCTCCCGCCTC T A RC3H2 Ensembl:ENSG00000056586 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1316728357 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110472,RMVar_hsa_circ_259276 48644 RMVar_ID_48644 Human_SNP_ID_414501522 A-to-I Human chr9 - 122902643 122902643 122902643 TTTGCCATGTTGACCAGGCTGGTCTGGAACTCATGACCTCAAGTGATCCACCCACCTCCCGCCTC TTTGCCATGTTGACCAGGCTGGTCTGGAACTCGTGACCTCAAGTGATCCACCCACCTCCCGCCTC T C RC3H2 Ensembl:ENSG00000056586 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1316728357 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110472,RMVar_hsa_circ_259276 48645 RMVar_ID_48645 Human_SNP_ID_414501567 A-to-I Human chr9 - 122902832 122902832 122902832 TTTTTTTTTTTTTTTTGAGACAGTCTCTCTCTATCACCCATGCTGGAGTGCAGTGGCACCATTCG TTTTTTTTTTTTTTTTGAGACAGTCTCTCTCTGTCACCCATGCTGGAGTGCAGTGGCACCATTCG T C RC3H2 Ensembl:ENSG00000056586 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1031052865 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110472,RMVar_hsa_circ_259276 48646 RMVar_ID_48646 Human_SNP_ID_414511852 A-to-I Human chr9 + 122943229 122943229 122943229 GCTTGGGATTACAGGCGTGTGCCACCACGCCTAGCTAATTTTTTGTATTTTTACTAGAGACGGGG GCTTGGGATTACAGGCGTGTGCCACCACGCCTTGCTAATTTTTTGTATTTTTACTAGAGACGGGG A T RABGAP1 Ensembl:ENSG00000011454 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs962082338 Functional Loss SNV dbSNP153 33..33 33 - - - 48647 RMVar_ID_48647 Human_SNP_ID_414512203 A-to-I Human chr9 + 122944363 122944363 122944363 GTGATCCTCCTGCTTCAGCCTCCCAAGTAGCTAGGACTGCAGGCACATGCGACCACACCCAGTGA GTGATCCTCCTGCTTCAGCCTCCCAAGTAGCTGGGACTGCAGGCACATGCGACCACACCCAGTGA A G RABGAP1 Ensembl:ENSG00000011454 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs868649550 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16557815 48648 RMVar_ID_48648 Human_SNP_ID_414514199 A-to-I Human chr9 + 122951674 122951674 122951674 TTCACTGCAGCCTAGAACCCCTGGACTCAAGCAGTCCTCTGGCTCAGCCTCCCAAGTAGCTGGCA TTCACTGCAGCCTAGAACCCCTGGACTCAAGCTGTCCTCTGGCTCAGCCTCCCAAGTAGCTGGCA A T RABGAP1 Ensembl:ENSG00000011454 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1161665406 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69039 48649 RMVar_ID_48649 Human_SNP_ID_414517246 A-to-I Human chr9 + 122963595 122963594 122963596 TGAAATGAATGAAAATGCAGATACAATATACTAAGACTTATGGGATACAGCTTAAACAGTTCTAA TGAAATGAATGAAAATGCAGATACAATATACT__GACTTATGGGATACAGCTTAAACAGTTCTAA TAA T RABGAP1 Ensembl:ENSG00000011454 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1383442383 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_297465,RMVar_hsa_circ_311932,RMVar_hsa_circ_345409,RMVar_hsa_circ_347624,RMVar_hsa_circ_356700,RMVar_hsa_circ_349749,RMVar_hsa_circ_346939,RMVar_hsa_circ_324679,RMVar_hsa_circ_308101,RMVar_hsa_circ_302037,RMVar_hsa_circ_121831,RMVar_hsa_circ_286277,RMVar_hsa_circ_294051,RMVar_hsa_circ_286095,RMVar_hsa_circ_259287,RMVar_hsa_circ_259289,RMVar_hsa_circ_64354,RMVar_hsa_circ_259290,RMVar_hsa_circ_259288,RMVar_hsa_circ_259291,RMVar_hsa_circ_259285,RMVar_hsa_circ_259286,RMVar_hsa_circ_259284 48650 RMVar_ID_48650 Human_SNP_ID_414524358 A-to-I Human chr9 + 122991706 122991706 122991706 CTCACTGCAGCCTCAGCCTTCTGGTCTCAAGCAGTCCTCCCACCTCGCCCTCCTGAGTAGCTGGG CTCACTGCAGCCTCAGCCTTCTGGTCTCAAGCGGTCCTCCCACCTCGCCCTCCTGAGTAGCTGGG A G RABGAP1 Ensembl:ENSG00000011454 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1256651554 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64857,RMVar_hsa_circ_311932,RMVar_hsa_circ_347624,RMVar_hsa_circ_356700,RMVar_hsa_circ_349749,RMVar_hsa_circ_346939,RMVar_hsa_circ_324679,RMVar_hsa_circ_308101,RMVar_hsa_circ_121831,RMVar_hsa_circ_286277,RMVar_hsa_circ_294051,RMVar_hsa_circ_259287,RMVar_hsa_circ_64354,RMVar_hsa_circ_259288,RMVar_hsa_circ_259291,RMVar_hsa_circ_259285,RMVar_hsa_circ_259286,RMVar_hsa_circ_259284,RMVar_hsa_circ_327887,RMVar_hsa_circ_273249,RMVar_hsa_circ_19439,RMVar_hsa_circ_126303,RMVar_hsa_circ_259292,RMVar_hsa_circ_121614,RMVar_hsa_circ_259293,RMVar_hsa_circ_259294,RMVar_hsa_circ_320063,RMVar_hsa_circ_367187,RMVar_hsa_circ_103323,RMVar_hsa_circ_41274,RMVar_hsa_circ_259296,RMVar_hsa_circ_259297 48651 RMVar_ID_48651 Human_SNP_ID_414525338 A-to-I Human chr9 + 122995730 122995730 122995730 AGCTGGGACTGTAGGCATGTGCCATCACACCCAGCTAATTTTTGTATTTTTAACAGAGATGGGGT AGCTGGGACTGTAGGCATGTGCCATCACACCCGGCTAATTTTTGTATTTTTAACAGAGATGGGGT A G RABGAP1 Ensembl:ENSG00000011454 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1261500497 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64857,RMVar_hsa_circ_311932,RMVar_hsa_circ_347624,RMVar_hsa_circ_356700,RMVar_hsa_circ_349749,RMVar_hsa_circ_346939,RMVar_hsa_circ_324679,RMVar_hsa_circ_308101,RMVar_hsa_circ_121831,RMVar_hsa_circ_286277,RMVar_hsa_circ_294051,RMVar_hsa_circ_259287,RMVar_hsa_circ_64354,RMVar_hsa_circ_259288,RMVar_hsa_circ_259291,RMVar_hsa_circ_259285,RMVar_hsa_circ_259286,RMVar_hsa_circ_259284,RMVar_hsa_circ_327887,RMVar_hsa_circ_273249,RMVar_hsa_circ_19439,RMVar_hsa_circ_126303,RMVar_hsa_circ_259292,RMVar_hsa_circ_121614,RMVar_hsa_circ_259293,RMVar_hsa_circ_259294,RMVar_hsa_circ_320063,RMVar_hsa_circ_367187,RMVar_hsa_circ_103323,RMVar_hsa_circ_41274,RMVar_hsa_circ_259296,RMVar_hsa_circ_259297 48652 RMVar_ID_48652 Human_SNP_ID_414532208 A-to-I Human chr9 + 123023451 123023451 123023451 GATCCCTCCCCTCCCTGGCCTCCCAAAGTGCTAGGATTACAGACGTGAGCCACCACACCCATCCT GATCCCTCCCCTCCCTGGCCTCCCAAAGTGCTGGGATTACAGACGTGAGCCACCACACCCATCCT A G RABGAP1 Ensembl:ENSG00000011454 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs964499438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_711183,Human_RBP_ID_16558971,Human_RBP_ID_26200487 RMVar_hsa_circ_311932,RMVar_hsa_circ_347624,RMVar_hsa_circ_308101,RMVar_hsa_circ_121831,RMVar_hsa_circ_64354,RMVar_hsa_circ_259284,RMVar_hsa_circ_126303,RMVar_hsa_circ_121614,RMVar_hsa_circ_259293,RMVar_hsa_circ_259294,RMVar_hsa_circ_103323,RMVar_hsa_circ_259297,RMVar_hsa_circ_285343,RMVar_hsa_circ_363744,RMVar_hsa_circ_40721,RMVar_hsa_circ_338536,RMVar_hsa_circ_26012,RMVar_hsa_circ_259306,RMVar_hsa_circ_259304,RMVar_hsa_circ_259298,RMVar_hsa_circ_374036,RMVar_hsa_circ_65283,RMVar_hsa_circ_281343,RMVar_hsa_circ_360798,RMVar_hsa_circ_350362,RMVar_hsa_circ_259309,RMVar_hsa_circ_370598,RMVar_hsa_circ_349048,RMVar_hsa_circ_343550,RMVar_hsa_circ_259313,RMVar_hsa_circ_298316,RMVar_hsa_circ_259311,RMVar_hsa_circ_259312,RMVar_hsa_circ_259310,RMVar_hsa_circ_310948 48653 RMVar_ID_48653 Human_SNP_ID_414532913 A-to-I Human chr9 + 123026256 123026256 123026256 TGAGGCAGGAGAATCGCTTGAACCCCGGAGGCAGAGGTTGCAGTGAGCCAAAATAGTGCCACTGC TGAGGCAGGAGAATCGCTTGAACCCCGGAGGCGGAGGTTGCAGTGAGCCAAAATAGTGCCACTGC A G RABGAP1 Ensembl:ENSG00000011454 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215414701 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_311932,RMVar_hsa_circ_347624,RMVar_hsa_circ_308101,RMVar_hsa_circ_121831,RMVar_hsa_circ_64354,RMVar_hsa_circ_259284,RMVar_hsa_circ_126303,RMVar_hsa_circ_121614,RMVar_hsa_circ_259293,RMVar_hsa_circ_259294,RMVar_hsa_circ_103323,RMVar_hsa_circ_259297,RMVar_hsa_circ_285343,RMVar_hsa_circ_363744,RMVar_hsa_circ_40721,RMVar_hsa_circ_338536,RMVar_hsa_circ_26012,RMVar_hsa_circ_259306,RMVar_hsa_circ_259304,RMVar_hsa_circ_259298,RMVar_hsa_circ_374036,RMVar_hsa_circ_65283,RMVar_hsa_circ_281343,RMVar_hsa_circ_360798,RMVar_hsa_circ_350362,RMVar_hsa_circ_259309,RMVar_hsa_circ_370598,RMVar_hsa_circ_349048,RMVar_hsa_circ_343550,RMVar_hsa_circ_259313,RMVar_hsa_circ_298316,RMVar_hsa_circ_259311,RMVar_hsa_circ_259312,RMVar_hsa_circ_259310,RMVar_hsa_circ_310948 48654 RMVar_ID_48654 Human_SNP_ID_414573851 A-to-I Human chr9 - 123203346 123203346 123203346 GTAATTTAGATTCTTTTTTTTTTTTCTTTTTTAGGGATGGGATCTTGCTGTGTTACCCAGGCTGG GTAATTTAGATTCTTTTTTTTTTTTCTTTTTTTGGGATGGGATCTTGCTGTGTTACCCAGGCTGG T A STRBP Ensembl:ENSG00000165209 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1214292608 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7894910 RMVar_hsa_circ_259333,RMVar_hsa_circ_259352,RMVar_hsa_circ_86690,RMVar_hsa_circ_259361,RMVar_hsa_circ_108790,RMVar_hsa_circ_259367 48655 RMVar_ID_48655 Human_SNP_ID_414574720 A-to-I Human chr9 - 123206777 123206777 123206777 AAAATTAGCTGAGCGTGGTGGCGGGTGCCTGTAATTCCAGCTACTCAGGAGGCTGAGGCAGGAGA AAAATTAGCTGAGCGTGGTGGCGGGTGCCTGTGATTCCAGCTACTCAGGAGGCTGAGGCAGGAGA T C STRBP Ensembl:ENSG00000165209 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1403135906 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_259333,RMVar_hsa_circ_259352,RMVar_hsa_circ_86690,RMVar_hsa_circ_259361,RMVar_hsa_circ_108790,RMVar_hsa_circ_259367 48656 RMVar_ID_48656 Human_SNP_ID_414582798 A-to-I Human chr9 - 123240997 123240997 123240997 TTTTGTATTTTTAGTAAAGATCGAGTTTCTCCATGTTGGTCAGGCTGGTCATGAACTCCCAACCA TTTTGTATTTTTAGTAAAGATCGAGTTTCTCCGTGTTGGTCAGGCTGGTCATGAACTCCCAACCA T C STRBP Ensembl:ENSG00000165209 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs920547493 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16561633 48657 RMVar_ID_48657 Human_SNP_ID_414585082 A-to-I Human chr9 - 123251011 123251011 123251011 GTGGTCTGCCTGCCTCAGCCTCACAAGTAGTTAGGATTACAGGATTACCAGACCTGGCTAATTAA GTGGTCTGCCTGCCTCAGCCTCACAAGTAGTTGGGATTACAGGATTACCAGACCTGGCTAATTAA T C STRBP Ensembl:ENSG00000165209 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934113073 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16561850,Human_RBP_ID_17174527 48658 RMVar_ID_48658 Human_SNP_ID_414662968 A-to-I Human chr9 - 123545746 123545746 123545746 AGGAGATCTTGGGAATGGGCGTGGTGTCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGT AGGAGATCTTGGGAATGGGCGTGGTGTCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGT T C DENND1A Ensembl:ENSG00000119522 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1010019620 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 48659 RMVar_ID_48659 Human_SNP_ID_414673398 A-to-I Human chr9 - 123588607 123588607 123588607 CCCCCCTTTTTTTTTTTTTGAGATGGAGTTTCACTCTTGTCACCTAGGCTGGAGTGCAATGGTGC CCCCCCTTTTTTTTTTTTTGAGATGGAGTTTCGCTCTTGTCACCTAGGCTGGAGTGCAATGGTGC T C DENND1A Ensembl:ENSG00000119522 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1188782089 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1504,RMVar_hsa_circ_104643,RMVar_hsa_circ_259371,RMVar_hsa_circ_365929,RMVar_hsa_circ_103766,RMVar_hsa_circ_259377,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_118721,RMVar_hsa_circ_283561,RMVar_hsa_circ_327372,RMVar_hsa_circ_259390,RMVar_hsa_circ_332724,RMVar_hsa_circ_286785,RMVar_hsa_circ_276342,RMVar_hsa_circ_276955,RMVar_hsa_circ_42347,RMVar_hsa_circ_110084,RMVar_hsa_circ_36566,RMVar_hsa_circ_259391,RMVar_hsa_circ_259393,RMVar_hsa_circ_259395,RMVar_hsa_circ_259396,RMVar_hsa_circ_259394,RMVar_hsa_circ_259392,RMVar_hsa_circ_282912,RMVar_hsa_circ_329899,RMVar_hsa_circ_347333,RMVar_hsa_circ_363520,RMVar_hsa_circ_328823,RMVar_hsa_circ_271358,RMVar_hsa_circ_259398,RMVar_hsa_circ_259400,RMVar_hsa_circ_259401,RMVar_hsa_circ_259399,RMVar_hsa_circ_259397 48660 RMVar_ID_48660 Human_SNP_ID_414675943 A-to-I Human chr9 - 123599417 123599417 123599417 ATCTCTAGAAGATAGCTCAACAGTCGTTTTGTACAAAGAGGTCAAACTGTGATGTAGTAACCATG ATCTCTAGAAGATAGCTCAACAGTCGTTTTGTGCAAAGAGGTCAAACTGTGATGTAGTAACCATG T C DENND1A Ensembl:ENSG00000119522 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1481482066 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1504,RMVar_hsa_circ_104643,RMVar_hsa_circ_259371,RMVar_hsa_circ_365929,RMVar_hsa_circ_103766,RMVar_hsa_circ_259377,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_118721,RMVar_hsa_circ_283561,RMVar_hsa_circ_327372,RMVar_hsa_circ_259390,RMVar_hsa_circ_332724,RMVar_hsa_circ_286785,RMVar_hsa_circ_276342,RMVar_hsa_circ_276955,RMVar_hsa_circ_42347,RMVar_hsa_circ_110084,RMVar_hsa_circ_36566,RMVar_hsa_circ_259391,RMVar_hsa_circ_259393,RMVar_hsa_circ_259395,RMVar_hsa_circ_259396,RMVar_hsa_circ_259394,RMVar_hsa_circ_259392,RMVar_hsa_circ_282912,RMVar_hsa_circ_329899,RMVar_hsa_circ_347333,RMVar_hsa_circ_363520,RMVar_hsa_circ_328823,RMVar_hsa_circ_271358,RMVar_hsa_circ_259398,RMVar_hsa_circ_259400,RMVar_hsa_circ_259401,RMVar_hsa_circ_259399,RMVar_hsa_circ_259397 48661 RMVar_ID_48661 Human_SNP_ID_414701090 A-to-I Human chr9 - 123706582 123706582 123706582 TATTTTTAGTAGAGACCGGGTTTCGCTGTGTTAGCCAGGATGGTCTCGATTTCCTGACCTCGTGA TATTTTTAGTAGAGACCGGGTTTCGCTGTGTTGGCCAGGATGGTCTCGATTTCCTGACCTCGTGA T C DENND1A Ensembl:ENSG00000119522 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs769738457 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104643,RMVar_hsa_circ_259371,RMVar_hsa_circ_365929,RMVar_hsa_circ_313042,RMVar_hsa_circ_59256,RMVar_hsa_circ_115401,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_28127,RMVar_hsa_circ_116681,RMVar_hsa_circ_259389,RMVar_hsa_circ_76560,RMVar_hsa_circ_118721,RMVar_hsa_circ_327372,RMVar_hsa_circ_259390,RMVar_hsa_circ_276342,RMVar_hsa_circ_42347,RMVar_hsa_circ_110084,RMVar_hsa_circ_8696,RMVar_hsa_circ_259391,RMVar_hsa_circ_259392,RMVar_hsa_circ_282912,RMVar_hsa_circ_363520,RMVar_hsa_circ_259401,RMVar_hsa_circ_369734,RMVar_hsa_circ_375695,RMVar_hsa_circ_371986,RMVar_hsa_circ_111189,RMVar_hsa_circ_313405,RMVar_hsa_circ_259409,RMVar_hsa_circ_97849,RMVar_hsa_circ_259403,RMVar_hsa_circ_259405,RMVar_hsa_circ_259406,RMVar_hsa_circ_259404,RMVar_hsa_circ_375568,RMVar_hsa_circ_259402,RMVar_hsa_circ_373343,RMVar_hsa_circ_306635,RMVar_hsa_circ_274318,RMVar_hsa_circ_259413,RMVar_hsa_circ_259411,RMVar_hsa_circ_259412,RMVar_hsa_circ_259410,RMVar_hsa_circ_53429,RMVar_hsa_circ_259421,RMVar_hsa_circ_278271,RMVar_hsa_circ_297289,RMVar_hsa_circ_329008,RMVar_hsa_circ_13357,RMVar_hsa_circ_353868,RMVar_hsa_circ_259420,RMVar_hsa_circ_333799,RMVar_hsa_circ_289634,RMVar_hsa_circ_259424,RMVar_hsa_circ_63102,RMVar_hsa_circ_45718,RMVar_hsa_circ_274725,RMVar_hsa_circ_259426 48662 RMVar_ID_48662 Human_SNP_ID_414703425 A-to-I Human chr9 - 123715903 123715903 123715903 GGGAGGCTGAGGTGGGGGGATCGCTTGAGGCCAGGAGTTTGAGACCACCCTGGGCAACATGGCAA GGGAGGCTGAGGTGGGGGGATCGCTTGAGGCCGGGAGTTTGAGACCACCCTGGGCAACATGGCAA T C DENND1A Ensembl:ENSG00000119522 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1298846098 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104643,RMVar_hsa_circ_259371,RMVar_hsa_circ_365929,RMVar_hsa_circ_313042,RMVar_hsa_circ_59256,RMVar_hsa_circ_115401,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_28127,RMVar_hsa_circ_116681,RMVar_hsa_circ_259389,RMVar_hsa_circ_76560,RMVar_hsa_circ_118721,RMVar_hsa_circ_327372,RMVar_hsa_circ_259390,RMVar_hsa_circ_276342,RMVar_hsa_circ_42347,RMVar_hsa_circ_110084,RMVar_hsa_circ_8696,RMVar_hsa_circ_259391,RMVar_hsa_circ_259392,RMVar_hsa_circ_282912,RMVar_hsa_circ_363520,RMVar_hsa_circ_259401,RMVar_hsa_circ_369734,RMVar_hsa_circ_375695,RMVar_hsa_circ_371986,RMVar_hsa_circ_111189,RMVar_hsa_circ_313405,RMVar_hsa_circ_259409,RMVar_hsa_circ_97849,RMVar_hsa_circ_259403,RMVar_hsa_circ_259405,RMVar_hsa_circ_259406,RMVar_hsa_circ_259404,RMVar_hsa_circ_375568,RMVar_hsa_circ_259402,RMVar_hsa_circ_373343,RMVar_hsa_circ_306635,RMVar_hsa_circ_274318,RMVar_hsa_circ_259413,RMVar_hsa_circ_259411,RMVar_hsa_circ_259412,RMVar_hsa_circ_259410,RMVar_hsa_circ_53429,RMVar_hsa_circ_259421,RMVar_hsa_circ_278271,RMVar_hsa_circ_297289,RMVar_hsa_circ_329008,RMVar_hsa_circ_13357,RMVar_hsa_circ_353868,RMVar_hsa_circ_259420,RMVar_hsa_circ_333799,RMVar_hsa_circ_289634,RMVar_hsa_circ_259424,RMVar_hsa_circ_63102,RMVar_hsa_circ_45718,RMVar_hsa_circ_274725,RMVar_hsa_circ_259426 48663 RMVar_ID_48663 Human_SNP_ID_414749431 A-to-I Human chr9 - 123919350 123919350 123919350 CTCCTGCCTCAACCTCCCCAGTAGCTGGGATTACAGGTGTGCGCCACCATGCCCAGCTAATTTTT CTCCTGCCTCAACCTCCCCAGTAGCTGGGATTGCAGGTGTGCGCCACCATGCCCAGCTAATTTTT T C DENND1A Ensembl:ENSG00000119522 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1016770051 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 48664 RMVar_ID_48664 Human_SNP_ID_414749765 A-to-I Human chr9 - 123920697 123920697 123920697 AAATTAGCTGGGCATGGTGGCGCATGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGTGTGAGAA AAATTAGCTGGGCATGGTGGCGCATGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGTGTGAGAA T C DENND1A Ensembl:ENSG00000119522 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1478495444 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 48665 RMVar_ID_48665 Human_SNP_ID_414846090 A-to-I Human chr9 + 124287663 124287662 124287663 CCTGGCCAACATGGTGAAACCCCATCTTTACTAAAAATAGAAAGATTTGCTGGGTGTAGTGGCAT CCTGGCCAACATGGTGAAACCCCATCTTTACT_AAAATAGAAAGATTTGCTGGGTGTAGTGGCAT TA T NEK6 Ensembl:ENSG00000119408 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1324281671 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_113771,RMVar_hsa_circ_259439 48666 RMVar_ID_48666 Human_SNP_ID_414846091 A-to-I Human chr9 + 124287669 124287669 124287669 CAACATGGTGAAACCCCATCTTTACTAAAAATAGAAAGATTTGCTGGGTGTAGTGGCATGCAGGT CAACATGGTGAAACCCCATCTTTACTAAAAATGGAAAGATTTGCTGGGTGTAGTGGCATGCAGGT A G NEK6 Ensembl:ENSG00000119408 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs756624312 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113771,RMVar_hsa_circ_259439 48667 RMVar_ID_48667 Human_SNP_ID_414846290 A-to-I Human chr9 + 124288470 124288470 124288470 ACACCCAGCTAATTTTTTGTATTTTTAGTAAAAATGGGGTTTTGCCATGTTGGCCAGGCTGGTCT ACACCCAGCTAATTTTTTGTATTTTTAGTAAAGATGGGGTTTTGCCATGTTGGCCAGGCTGGTCT A G NEK6 Ensembl:ENSG00000119408 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1340761371 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113771,RMVar_hsa_circ_259439 48668 RMVar_ID_48668 Human_SNP_ID_414852997 A-to-I Human chr9 + 124313954 124313954 124313954 GATCTTTGAGATGATGGACGCCAAGGCGAGGCAGGACTGTGTCAAGGAGATCGGCCTCTTGAAGG GATCTTTGAGATGATGGACGCCAAGGCGAGGCGGGACTGTGTCAAGGAGATCGGCCTCTTGAAGG A G NEK6 Ensembl:ENSG00000119408 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs987052518 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_711354,Human_RBP_ID_963741,Human_RBP_ID_18141214,Human_RBP_ID_19025554,Human_RBP_ID_19143820 Human_Splice_Rec_1079080,Human_Splice_Rec_1079081,Human_Splice_Rec_1079098,Human_Splice_Rec_1079099,Human_Splice_Rec_1079118,Human_Splice_Rec_1079119,Human_Splice_Rec_1079136,Human_Splice_Rec_1079137,Human_Splice_Rec_1079154,Human_Splice_Rec_1079155,Human_Splice_Rec_1079172,Human_Splice_Rec_1079173,Human_Splice_Rec_1079198,Human_Splice_Rec_1079199,Human_Splice_Rec_1079210,Human_Splice_Rec_1079211,Human_Splice_Rec_1079226,Human_Splice_Rec_1079227,Human_Splice_Rec_1079236,Human_Splice_Rec_1079237,Human_Splice_Rec_1079254,Human_Splice_Rec_1079255,Human_Splice_Rec_1079268,Human_Splice_Rec_1079269,Human_Splice_Rec_1079286,Human_Splice_Rec_1079287,Human_Splice_Rec_1079304,Human_Splice_Rec_1079305 Human_miRNA_ID_2782482,Human_miRNA_ID_2782483,Human_miRNA_ID_2785450,Human_miRNA_ID_2785451 RMVar_hsa_circ_259445,RMVar_hsa_circ_22015,RMVar_hsa_circ_113771,RMVar_hsa_circ_116604,RMVar_hsa_circ_259439,RMVar_hsa_circ_338596,RMVar_hsa_circ_259440,RMVar_hsa_circ_341141,RMVar_hsa_circ_47270,RMVar_hsa_circ_270013,RMVar_hsa_circ_321337,RMVar_hsa_circ_259441,RMVar_hsa_circ_336561,RMVar_hsa_circ_301868,RMVar_hsa_circ_311620,RMVar_hsa_circ_299765,RMVar_hsa_circ_259447,RMVar_hsa_circ_259448,RMVar_hsa_circ_259446,RMVar_hsa_circ_32889,RMVar_hsa_circ_259443,RMVar_hsa_circ_259444,RMVar_hsa_circ_277241,RMVar_hsa_circ_376868,RMVar_hsa_circ_356819,RMVar_hsa_circ_274512,RMVar_hsa_circ_15403,RMVar_hsa_circ_259449,RMVar_hsa_circ_259450,RMVar_hsa_circ_128002,RMVar_hsa_circ_372853,RMVar_hsa_circ_259451,RMVar_hsa_circ_5449,RMVar_hsa_circ_259452 48669 RMVar_ID_48669 Human_SNP_ID_414857729 A-to-I Human chr9 + 124331711 124331711 124331711 TGTGTCAGCGCTGCCTTGCCGGGGATCACACCATGCTGTGCTGCGTCTGTGCCCAGGCCTGGCAT TGTGTCAGCGCTGCCTTGCCGGGGATCACACCGTGCTGTGCTGCGTCTGTGCCCAGGCCTGGCAT A G NEK6 Ensembl:ENSG00000119408 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4838163 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_341141,RMVar_hsa_circ_47270,RMVar_hsa_circ_321337,RMVar_hsa_circ_259441,RMVar_hsa_circ_336561,RMVar_hsa_circ_259447,RMVar_hsa_circ_259448,RMVar_hsa_circ_356819,RMVar_hsa_circ_5449,RMVar_hsa_circ_365008,RMVar_hsa_circ_61552 48670 RMVar_ID_48670 Human_SNP_ID_414857730 A-to-I Human chr9 + 124331711 124331711 124331711 TGTGTCAGCGCTGCCTTGCCGGGGATCACACCATGCTGTGCTGCGTCTGTGCCCAGGCCTGGCAT TGTGTCAGCGCTGCCTTGCCGGGGATCACACCTTGCTGTGCTGCGTCTGTGCCCAGGCCTGGCAT A T NEK6 Ensembl:ENSG00000119408 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4838163 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_341141,RMVar_hsa_circ_47270,RMVar_hsa_circ_321337,RMVar_hsa_circ_259441,RMVar_hsa_circ_336561,RMVar_hsa_circ_259447,RMVar_hsa_circ_259448,RMVar_hsa_circ_356819,RMVar_hsa_circ_5449,RMVar_hsa_circ_365008,RMVar_hsa_circ_61552 48671 RMVar_ID_48671 Human_SNP_ID_414858304 A-to-I Human chr9 + 124333842 124333842 124333842 CTCTGTTGCCCAAGCTGGAATGCAGTGGTGCGATCTCGGCTCACTACAACCTTCACCTCCCGGGT CTCTGTTGCCCAAGCTGGAATGCAGTGGTGCGGTCTCGGCTCACTACAACCTTCACCTCCCGGGT A G NEK6 Ensembl:ENSG00000119408 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs973557706 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_341141,RMVar_hsa_circ_47270,RMVar_hsa_circ_321337,RMVar_hsa_circ_259441,RMVar_hsa_circ_336561,RMVar_hsa_circ_259447,RMVar_hsa_circ_259448,RMVar_hsa_circ_356819,RMVar_hsa_circ_5449,RMVar_hsa_circ_365008,RMVar_hsa_circ_61552 48672 RMVar_ID_48672 Human_SNP_ID_414859318 A-to-I Human chr9 + 124338130 124338130 124338130 AGCCTCCTGAGTAGCTGGGATGACAGGTGTGTACCACCATGCCTGGCTAATTTTTGTGTTTTTAG AGCCTCCTGAGTAGCTGGGATGACAGGTGTGTGCCACCATGCCTGGCTAATTTTTGTGTTTTTAG A G NEK6 Ensembl:ENSG00000119408 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs748430733 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_341141,RMVar_hsa_circ_47270,RMVar_hsa_circ_321337,RMVar_hsa_circ_259441,RMVar_hsa_circ_336561,RMVar_hsa_circ_259447,RMVar_hsa_circ_259448,RMVar_hsa_circ_356819,RMVar_hsa_circ_5449,RMVar_hsa_circ_365008,RMVar_hsa_circ_61552 48673 RMVar_ID_48673 Human_SNP_ID_414859325 A-to-I Human chr9 + 124338170 124338169 124338171 GCCTGGCTAATTTTTGTGTTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCATGCTGGTCTCAA GCCTGGCTAATTTTTGTGTTTTTAGTAGAGAC__GGTTTCACCATGTTGGCCATGCTGGTCTCAA CAG C NEK6 Ensembl:ENSG00000119408 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1327164420 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_341141,RMVar_hsa_circ_47270,RMVar_hsa_circ_321337,RMVar_hsa_circ_259441,RMVar_hsa_circ_336561,RMVar_hsa_circ_259447,RMVar_hsa_circ_259448,RMVar_hsa_circ_356819,RMVar_hsa_circ_5449,RMVar_hsa_circ_365008,RMVar_hsa_circ_61552 48674 RMVar_ID_48674 Human_SNP_ID_414859327 A-to-I Human chr9 + 124338170 124338170 124338170 GCCTGGCTAATTTTTGTGTTTTTAGTAGAGACAGGGTTTCACCATGTTGGCCATGCTGGTCTCAA GCCTGGCTAATTTTTGTGTTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCATGCTGGTCTCAA A G NEK6 Ensembl:ENSG00000119408 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1047024218 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_341141,RMVar_hsa_circ_47270,RMVar_hsa_circ_321337,RMVar_hsa_circ_259441,RMVar_hsa_circ_336561,RMVar_hsa_circ_259447,RMVar_hsa_circ_259448,RMVar_hsa_circ_356819,RMVar_hsa_circ_5449,RMVar_hsa_circ_365008,RMVar_hsa_circ_61552 48675 RMVar_ID_48675 Human_SNP_ID_414864535 A-to-I Human chr9 + 124356278 124356277 124356278 CACCACTGAGCCGAGGGGCCCACTCGGCATGTAGGCTCAGGCTCAATGGCACAACTCCCTGTAGC CACCACTGAGCCGAGGGGCCCACTCGGCATGT_GGCTCAGGCTCAATGGCACAACTCCCTGTAGC TA T LOC100129034,LOC100129034:2,LOC100129034:3 RNACentral:URS00008BBF99,RNACentral:URS00008C109E,RNACentral:URS000075AF90 lincRNA,lincRNA,lincRNA exon,intron,exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1485994606 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_17321104 48676 RMVar_ID_48676 Human_SNP_ID_414870382 A-to-I Human chr9 - 124382038 124382038 124382038 CCCAGGTGGGTCTGGAACTCCTGAGCTCAAGCAGTCTGCCTACCTTGGCCTCCCAAAGGCTGGGA CCCAGGTGGGTCTGGAACTCCTGAGCTCAAGCGGTCTGCCTACCTTGGCCTCCCAAAGGCTGGGA T C PSMB7 Ensembl:ENSG00000136930 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1406427074 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115570,RMVar_hsa_circ_124933,RMVar_hsa_circ_101207,RMVar_hsa_circ_19035,RMVar_hsa_circ_259458,RMVar_hsa_circ_259459,RMVar_hsa_circ_259457,RMVar_hsa_circ_31163 48677 RMVar_ID_48677 Human_SNP_ID_414870383 A-to-I Human chr9 - 124382042 124382042 124382042 GCTGCCCAGGTGGGTCTGGAACTCCTGAGCTCAAGCAGTCTGCCTACCTTGGCCTCCCAAAGGCT GCTGCCCAGGTGGGTCTGGAACTCCTGAGCTCGAGCAGTCTGCCTACCTTGGCCTCCCAAAGGCT T C PSMB7 Ensembl:ENSG00000136930 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs936893838 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115570,RMVar_hsa_circ_124933,RMVar_hsa_circ_101207,RMVar_hsa_circ_19035,RMVar_hsa_circ_259458,RMVar_hsa_circ_259459,RMVar_hsa_circ_259457,RMVar_hsa_circ_31163 48678 RMVar_ID_48678 Human_SNP_ID_414870422 A-to-I Human chr9 - 124382182 124382179 124382183 AAAAAAAAAAAAAAGAGAAAAGAGAGAGAGACAGAGTCTCACTCTGTCATCCAGGCTGGAGTGCG AAAAAAAAAAAAAAGAGAAAAGAGAGAGAGA____GTCTCACTCTGTCATCCAGGCTGGAGTGCG CTCTG C PSMB7 Ensembl:ENSG00000136930 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1564680148 Functional Loss DEL dbSNP153 32..35 33 - - - RMVar_hsa_circ_115570,RMVar_hsa_circ_124933,RMVar_hsa_circ_101207,RMVar_hsa_circ_19035,RMVar_hsa_circ_259458,RMVar_hsa_circ_259459,RMVar_hsa_circ_259457,RMVar_hsa_circ_31163 48679 RMVar_ID_48679 Human_SNP_ID_414871654 A-to-I Human chr9 - 124387183 124387183 124387183 GGAGTGCAGTTGCGCGATCTGGGCTCACTGCAAACTCTGCCTCCCGGGTTCATGCCATTCTCCTG GGAGTGCAGTTGCGCGATCTGGGCTCACTGCATACTCTGCCTCCCGGGTTCATGCCATTCTCCTG T A PSMB7 Ensembl:ENSG00000136930 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1168721375 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115570,RMVar_hsa_circ_124933,RMVar_hsa_circ_19035,RMVar_hsa_circ_259458,RMVar_hsa_circ_259459,RMVar_hsa_circ_79197,RMVar_hsa_circ_373208,RMVar_hsa_circ_259461,RMVar_hsa_circ_52569,RMVar_hsa_circ_259460 48680 RMVar_ID_48680 Human_SNP_ID_414875432 A-to-I Human chr9 - 124403967 124403967 124403967 GCATTGTATGAGCCCAGGAGTTTGAGGTTGCAATGAGCTGTGATCAAGCCATTGTACTACATCTT GCATTGTATGAGCCCAGGAGTTTGAGGTTGCAGTGAGCTGTGATCAAGCCATTGTACTACATCTT T C PSMB7 Ensembl:ENSG00000136930 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs530829003 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3899,RMVar_hsa_circ_115570,RMVar_hsa_circ_124933,RMVar_hsa_circ_19035,RMVar_hsa_circ_259458,RMVar_hsa_circ_259459,RMVar_hsa_circ_79197,RMVar_hsa_circ_373208,RMVar_hsa_circ_259461,RMVar_hsa_circ_52569,RMVar_hsa_circ_259460 48681 RMVar_ID_48681 Human_SNP_ID_414931325 A-to-I Human chr9 - 124621591 124621591 124621591 CCAGTGCAGTGGTATGGTCACAGCTCACTGCAACTTCAACCTCCTTGGCTGAAGTGATACTCCCA CCAGTGCAGTGGTATGGTCACAGCTCACTGCAGCTTCAACCTCCTTGGCTGAAGTGATACTCCCA T C NR6A1 Ensembl:ENSG00000148200 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1406729981 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16567312 RMVar_hsa_circ_259471,RMVar_hsa_circ_105444 48682 RMVar_ID_48682 Human_SNP_ID_414937796 A-to-I Human chr9 - 124647644 124647644 124647644 CGGCTCACTGCAACCTCCGATTCCCAGGTTCAAGTGATTCCCCTGCCTCAGCTTCTGAGTAGCTG CGGCTCACTGCAACCTCCGATTCCCAGGTTCAGGTGATTCCCCTGCCTCAGCTTCTGAGTAGCTG T C NR6A1 Ensembl:ENSG00000148200 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215412348 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_259471,RMVar_hsa_circ_105444 48683 RMVar_ID_48683 Human_SNP_ID_414954531 A-to-I Human chr9 - 124719178 124719178 124719178 GGAGGATCACTTGGTCCTGGGAGGTCGAGGCTACAGTGAGTTGTGATCGCACCACTGCACTCCAG GGAGGATCACTTGGTCCTGGGAGGTCGAGGCTGCAGTGAGTTGTGATCGCACCACTGCACTCCAG T C NR6A1 Ensembl:ENSG00000148200 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs961905557 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_259471,RMVar_hsa_circ_105444,RMVar_hsa_circ_259476 48684 RMVar_ID_48684 Human_SNP_ID_414956987 A-to-I Human chr9 - 124729570 124729570 124729570 ATTTAATTTAATTTTTTTTGAGACAGGGTCTTACTCTTTTGTCCAAGCTGTAGTGCAGTGGCATA ATTTAATTTAATTTTTTTTGAGACAGGGTCTTTCTCTTTTGTCCAAGCTGTAGTGCAGTGGCATA T A NR6A1 Ensembl:ENSG00000148200 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978547852 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16569415 RMVar_hsa_circ_259471,RMVar_hsa_circ_105444,RMVar_hsa_circ_259476 48685 RMVar_ID_48685 Human_SNP_ID_414991680 A-to-I Human chr9 - 124858369 124858369 124858369 CATGTGACTGTCCTCGTGACTGGGAATCGGGCAGTGGAAGGAGCACTGAGTTGGGAGTCACTTGA CATGTGACTGTCCTCGTGACTGGGAATCGGGCGGTGGAAGGAGCACTGAGTTGGGAGTCACTTGA T C RPL35 Ensembl:ENSG00000136942 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs751670079 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1701885,Human_RBP_ID_7897076,Human_RBP_ID_8696378,Human_RBP_ID_16570932,Human_RBP_ID_18903435,Human_RBP_ID_23141336,Human_RBP_ID_24285129 Human_Splice_Rec_1079691 RMVar_hsa_circ_124949,RMVar_hsa_circ_122879,RMVar_hsa_circ_259478,RMVar_hsa_circ_259480,RMVar_hsa_circ_89612,RMVar_hsa_circ_259479 48686 RMVar_ID_48686 Human_SNP_ID_414999294 A-to-I Human chr9 - 124885384 124885384 124885384 GCCTCCTCGGTGCAAGCGATTCTGTTGCCTCAACCTCCCGAGTAGCTGTGATTACAGGTGCCCAC GCCTCCTCGGTGCAAGCGATTCTGTTGCCTCAGCCTCCCGAGTAGCTGTGATTACAGGTGCCCAC T C GOLGA1 Ensembl:ENSG00000136935 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1187755858 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89330,RMVar_hsa_circ_259485,RMVar_hsa_circ_259484,RMVar_hsa_circ_259486 48687 RMVar_ID_48687 Human_SNP_ID_414999315 A-to-I Human chr9 - 124885446 124885446 124885446 GAGTCTCCCCCTGTCACCCAGACTGGAGTGCAATGGCGTGATCTTGGCTCACTGCGACCTCTGCC GAGTCTCCCCCTGTCACCCAGACTGGAGTGCAGTGGCGTGATCTTGGCTCACTGCGACCTCTGCC T C GOLGA1 Ensembl:ENSG00000136935 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1416339417 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89330,RMVar_hsa_circ_259485,RMVar_hsa_circ_259484,RMVar_hsa_circ_259486 48688 RMVar_ID_48688 Human_SNP_ID_415005657 A-to-I Human chr9 - 124909525 124909525 124909525 GGCTCACTGCAACCTCTGCTTCCCGGGGTTCAAGTGATTTTCCTGCCTCAGCATCCCGAGTAGCT GGCTCACTGCAACCTCTGCTTCCCGGGGTTCAGGTGATTTTCCTGCCTCAGCATCCCGAGTAGCT T C GOLGA1 Ensembl:ENSG00000136935 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs995758813 Functional Loss SNV dbSNP153 33..33 33 - - - 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 48689 RMVar_ID_48689 Human_SNP_ID_415005658 A-to-I Human chr9 - 124909525 124909525 124909525 GGCTCACTGCAACCTCTGCTTCCCGGGGTTCAAGTGATTTTCCTGCCTCAGCATCCCGAGTAGCT GGCTCACTGCAACCTCTGCTTCCCGGGGTTCACGTGATTTTCCTGCCTCAGCATCCCGAGTAGCT T G GOLGA1 Ensembl:ENSG00000136935 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs995758813 Functional Loss SNV dbSNP153 33..33 33 - - - 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 48690 RMVar_ID_48690 Human_SNP_ID_415009288 A-to-I Human chr9 - 124923929 124923929 124923929 ATCACTTCAACCTGGGAGGCAGAGGATGCAGTAAGCTGAGATCTCACCACTGCAAACCAACCTGG ATCACTTCAACCTGGGAGGCAGAGGATGCAGTGAGCTGAGATCTCACCACTGCAAACCAACCTGG T C GOLGA1 Ensembl:ENSG00000136935 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs996068474 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2049,RMVar_hsa_circ_259485,RMVar_hsa_circ_72408,RMVar_hsa_circ_50603,RMVar_hsa_circ_267397,RMVar_hsa_circ_344722,RMVar_hsa_circ_259495,RMVar_hsa_circ_66326,RMVar_hsa_circ_314242,RMVar_hsa_circ_344943,RMVar_hsa_circ_259496,RMVar_hsa_circ_316007,RMVar_hsa_circ_55617,RMVar_hsa_circ_259500 48691 RMVar_ID_48691 Human_SNP_ID_415009290 A-to-I Human chr9 - 124923952 124923952 124923952 ACTCAGGAAGCTGAGGCATGAAAATCACTTCAACCTGGGAGGCAGAGGATGCAGTAAGCTGAGAT ACTCAGGAAGCTGAGGCATGAAAATCACTTCAGCCTGGGAGGCAGAGGATGCAGTAAGCTGAGAT T C GOLGA1 Ensembl:ENSG00000136935 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1338579348 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2049,RMVar_hsa_circ_259485,RMVar_hsa_circ_72408,RMVar_hsa_circ_50603,RMVar_hsa_circ_267397,RMVar_hsa_circ_344722,RMVar_hsa_circ_259495,RMVar_hsa_circ_66326,RMVar_hsa_circ_314242,RMVar_hsa_circ_344943,RMVar_hsa_circ_259496,RMVar_hsa_circ_316007,RMVar_hsa_circ_55617,RMVar_hsa_circ_259500 48692 RMVar_ID_48692 Human_SNP_ID_415009291 A-to-I Human chr9 - 124923953 124923953 124923953 TACTCAGGAAGCTGAGGCATGAAAATCACTTCAACCTGGGAGGCAGAGGATGCAGTAAGCTGAGA TACTCAGGAAGCTGAGGCATGAAAATCACTTCGACCTGGGAGGCAGAGGATGCAGTAAGCTGAGA T C GOLGA1 Ensembl:ENSG00000136935 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs536850691 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2049,RMVar_hsa_circ_259485,RMVar_hsa_circ_72408,RMVar_hsa_circ_50603,RMVar_hsa_circ_267397,RMVar_hsa_circ_344722,RMVar_hsa_circ_259495,RMVar_hsa_circ_66326,RMVar_hsa_circ_314242,RMVar_hsa_circ_344943,RMVar_hsa_circ_259496,RMVar_hsa_circ_316007,RMVar_hsa_circ_55617,RMVar_hsa_circ_259500 48693 RMVar_ID_48693 Human_SNP_ID_415014372 A-to-I Human chr9 - 124945446 124945446 124945446 GGTTCAAGAGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCGTGTGCCACCACGA GGTTCAAGAGATTCTCCTGCCTCAGCCTCCCAGGTAGCTGGGATTACAGGCGTGTGCCACCACGA T C GOLGA1,SCAI Ensembl:ENSG00000136935,Ensembl:ENSG00000173611 Protein coding,Protein coding intron,3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1428178900 Functional Loss SNV dbSNP153 33..33 33 - - - 48694 RMVar_ID_48694 Human_SNP_ID_415015345 A-to-I Human chr9 - 124950412 124950412 124950412 CTCCCCCGTTAAGCATAAAGAACACTGGTCTGAGAACTAGGAGACCTAAGTTCTAGTCCTGGCTT CTCCCCCGTTAAGCATAAAGAACACTGGTCTGTGAACTAGGAGACCTAAGTTCTAGTCCTGGCTT T A SCAI Ensembl:ENSG00000173611 Protein coding 3'UTR GSE100210;GSE107867;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,30559470,32596459 RNA-Seq:(High) rs1477906699 Functional Loss SNV dbSNP153 33..33 33 - - - 48695 RMVar_ID_48695 Human_SNP_ID_415037505 A-to-I Human chr9 - 125040270 125040270 125040270 TGCATGCAGCCTTGACCTCCAGGGTTCAAGCAATCCTCCCACCTCAGCCACCCAAGTAGCTGGGA TGCATGCAGCCTTGACCTCCAGGGTTCAAGCAGTCCTCCCACCTCAGCCACCCAAGTAGCTGGGA T C SCAI Ensembl:ENSG00000173611 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1260487391 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6186,RMVar_hsa_circ_31395,RMVar_hsa_circ_339028,RMVar_hsa_circ_259505,RMVar_hsa_circ_259506,RMVar_hsa_circ_111658,RMVar_hsa_circ_259512,RMVar_hsa_circ_97137,RMVar_hsa_circ_2187,RMVar_hsa_circ_259517,RMVar_hsa_circ_23338,RMVar_hsa_circ_99645,RMVar_hsa_circ_10798,RMVar_hsa_circ_259530,RMVar_hsa_circ_86336,RMVar_hsa_circ_259539,RMVar_hsa_circ_259534,RMVar_hsa_circ_355999,RMVar_hsa_circ_282918,RMVar_hsa_circ_259540,RMVar_hsa_circ_34811,RMVar_hsa_circ_92131,RMVar_hsa_circ_44171,RMVar_hsa_circ_30076,RMVar_hsa_circ_335808,RMVar_hsa_circ_259541,RMVar_hsa_circ_259546,RMVar_hsa_circ_25994,RMVar_hsa_circ_259547,RMVar_hsa_circ_317777,RMVar_hsa_circ_324432 48696 RMVar_ID_48696 Human_SNP_ID_415046697 A-to-I Human chr9 - 125077112 125077112 125077112 ACCATATGAGTGGGGACTGGCTCTGTCACCCAAGCCTGAGTGCAGTGGCGCTTCCAACTCACCTT ACCATATGAGTGGGGACTGGCTCTGTCACCCACGCCTGAGTGCAGTGGCGCTTCCAACTCACCTT T G SCAI Ensembl:ENSG00000173611 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1248890452 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99645,RMVar_hsa_circ_259530,RMVar_hsa_circ_92131,RMVar_hsa_circ_259541,RMVar_hsa_circ_96546,RMVar_hsa_circ_259549 48697 RMVar_ID_48697 Human_SNP_ID_415061243 A-to-I Human chr9 - 125135807 125135807 125135807 GCGCCACCACACCCAGCTAATTTTGTATTTTTAGTAGAGATGGGGTTTCTCCATGTTCGTTAGGC GCGCCACCACACCCAGCTAATTTTGTATTTTTGGTAGAGATGGGGTTTCTCCATGTTCGTTAGGC T C SCAI Ensembl:ENSG00000173611 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348346051 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99645,RMVar_hsa_circ_259530,RMVar_hsa_circ_92131,RMVar_hsa_circ_259541,RMVar_hsa_circ_96546,RMVar_hsa_circ_259549 48698 RMVar_ID_48698 Human_SNP_ID_415067368 A-to-I Human chr9 - 125158772 125158772 125158772 CTGTAATCCCAGCTACTCAGGAGTCTGAGGCAAGAGAATCGCTTGAACCCGGGAGGCGGAGGTTG CTGTAATCCCAGCTACTCAGGAGTCTGAGGCAGGAGAATCGCTTGAACCCGGGAGGCGGAGGTTG T C PPP6C Ensembl:ENSG00000119414 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1459705103 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_340876,RMVar_hsa_circ_310990,RMVar_hsa_circ_259552,RMVar_hsa_circ_259553,RMVar_hsa_circ_289466,RMVar_hsa_circ_357984 48699 RMVar_ID_48699 Human_SNP_ID_415067371 A-to-I Human chr9 - 125158786 125158786 125158786 GTGGCGGCTTGTACCTGTAATCCCAGCTACTCAGGAGTCTGAGGCAAGAGAATCGCTTGAACCCG GTGGCGGCTTGTACCTGTAATCCCAGCTACTCGGGAGTCTGAGGCAAGAGAATCGCTTGAACCCG T C PPP6C Ensembl:ENSG00000119414 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs552682296 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_340876,RMVar_hsa_circ_310990,RMVar_hsa_circ_259552,RMVar_hsa_circ_259553,RMVar_hsa_circ_289466,RMVar_hsa_circ_357984 48700 RMVar_ID_48700 Human_SNP_ID_415071351 A-to-I Human chr9 - 125172325 125172325 125172325 CTGTAATCCCAGGTACTTGTGAGACTGAGGCAAGGGAATCACTTGAACTGGGAGGCAGTTTGCAG CTGTAATCCCAGGTACTTGTGAGACTGAGGCAGGGGAATCACTTGAACTGGGAGGCAGTTTGCAG T C PPP6C Ensembl:ENSG00000119414 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1367471946 Functional Loss SNV dbSNP153 33..33 33 - - - 48701 RMVar_ID_48701 Human_SNP_ID_415074895 A-to-I Human chr9 - 125185642 125185642 125185642 TTGCCCAGGCTAGAGTGCAGGTGCACGTTCTCAGCTCACTGCAACCTCCGCCTCCCGGATTCAAG TTGCCCAGGCTAGAGTGCAGGTGCACGTTCTCGGCTCACTGCAACCTCCGCCTCCCGGATTCAAG T C PPP6C Ensembl:ENSG00000119414 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1416338138 Functional Loss SNV dbSNP153 33..33 33 - - - 48702 RMVar_ID_48702 Human_SNP_ID_415074915 A-to-I Human chr9 - 125185690 125185690 125185690 GTGAGCCTGGCCTGTTAGTTTGTTTTTTTGAGACGGAGTCTTGCTCTGTTGCCCAGGCTAGAGTG GTGAGCCTGGCCTGTTAGTTTGTTTTTTTGAGGCGGAGTCTTGCTCTGTTGCCCAGGCTAGAGTG T C PPP6C Ensembl:ENSG00000119414 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985875500 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16572794,Human_RBP_ID_18903538 48703 RMVar_ID_48703 Human_SNP_ID_415079990 A-to-I Human chr9 + 125203777 125203773 125203778 CTCCTGGGCTGGGCACGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGTGG CTCCTGGGCTGGGCACGGTGGCTCATGCC_____TCCCAGCACTTTGGGAGGCCAAGGCGGGTGG CTGTAA C RABEPK Ensembl:ENSG00000136933 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs561875827 Functional Loss DEL dbSNP153 30..34 33 - - - RMVar_hsa_circ_24400,RMVar_hsa_circ_79833,RMVar_hsa_circ_85622,RMVar_hsa_circ_68243,RMVar_hsa_circ_259555,RMVar_hsa_circ_259556,RMVar_hsa_circ_57457,RMVar_hsa_circ_259557,RMVar_hsa_circ_121418,RMVar_hsa_circ_373215,RMVar_hsa_circ_259558 48704 RMVar_ID_48704 Human_SNP_ID_415079992 A-to-I Human chr9 + 125203777 125203774 125203778 CTCCTGGGCTGGGCACGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGTGG CTCCTGGGCTGGGCACGGTGGCTCATGCCT____TCCCAGCACTTTGGGAGGCCAAGGCGGGTGG TGTAA T RABEPK Ensembl:ENSG00000136933 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs773830710 Functional Loss DEL dbSNP153 31..34 33 - - - RMVar_hsa_circ_24400,RMVar_hsa_circ_79833,RMVar_hsa_circ_85622,RMVar_hsa_circ_68243,RMVar_hsa_circ_259555,RMVar_hsa_circ_259556,RMVar_hsa_circ_57457,RMVar_hsa_circ_259557,RMVar_hsa_circ_121418,RMVar_hsa_circ_373215,RMVar_hsa_circ_259558 48705 RMVar_ID_48705 Human_SNP_ID_415080054 A-to-I Human chr9 + 125203987 125203987 125203987 CTGGGAGGCAGAGGTTGCAGTGAGCTGAGATCATGCCACTGTACTCCAGCATGGGCCACAGAGCA CTGGGAGGCAGAGGTTGCAGTGAGCTGAGATCCTGCCACTGTACTCCAGCATGGGCCACAGAGCA A C RABEPK Ensembl:ENSG00000136933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1377997106 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24400,RMVar_hsa_circ_79833,RMVar_hsa_circ_85622,RMVar_hsa_circ_68243,RMVar_hsa_circ_259555,RMVar_hsa_circ_259556,RMVar_hsa_circ_57457,RMVar_hsa_circ_259557,RMVar_hsa_circ_121418,RMVar_hsa_circ_373215,RMVar_hsa_circ_259558 48706 RMVar_ID_48706 Human_SNP_ID_415080669 A-to-I Human chr9 + 125206387 125206387 125206387 AGGCATGGTGGTGCGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAA AGGCATGGTGGTGCGCGCCTGTAGTCCCAGCTGCTCGGGAGGCTGAGGCAGGAGAATCACTTGAA A G RABEPK Ensembl:ENSG00000136933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs888018524 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24400,RMVar_hsa_circ_79833,RMVar_hsa_circ_85622,RMVar_hsa_circ_68243,RMVar_hsa_circ_259555,RMVar_hsa_circ_259556,RMVar_hsa_circ_57457,RMVar_hsa_circ_259557,RMVar_hsa_circ_121418,RMVar_hsa_circ_373215,RMVar_hsa_circ_259558 48707 RMVar_ID_48707 Human_SNP_ID_415081238 A-to-I Human chr9 + 125208675 125208663 125208676 CTCCTGCCTCAGCCTCCTGAGAAGCTGGGATTACAGGCGCCCACCACTACACCCAGCTAATCTTT CTCCTGCCTCAGCCTCCTGAG_____________AGGCGCCCACCACTACACCCAGCTAATCTTT GAAGCTGGGATTAC G RABEPK Ensembl:ENSG00000136933 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1479326965 Functional Loss DEL dbSNP153 22..34 33 - - - RMVar_hsa_circ_24400,RMVar_hsa_circ_79833,RMVar_hsa_circ_85622,RMVar_hsa_circ_259555,RMVar_hsa_circ_259556,RMVar_hsa_circ_57457,RMVar_hsa_circ_259562,RMVar_hsa_circ_307616,RMVar_hsa_circ_121418,RMVar_hsa_circ_259558,RMVar_hsa_circ_359781,RMVar_hsa_circ_375763,RMVar_hsa_circ_82717,RMVar_hsa_circ_287271,RMVar_hsa_circ_259563,RMVar_hsa_circ_259560,RMVar_hsa_circ_259561,RMVar_hsa_circ_259559 48708 RMVar_ID_48708 Human_SNP_ID_415081994 A-to-I Human chr9 + 125211279 125211279 125211279 GAAAGTGATTCTCCTGCCTCATACTCCCAAGTAGCTGGAACTACAGGCACGTGCCACCATGCCCC GAAAGTGATTCTCCTGCCTCATACTCCCAAGTCGCTGGAACTACAGGCACGTGCCACCATGCCCC A C RABEPK Ensembl:ENSG00000136933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1176073170 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24400,RMVar_hsa_circ_79833,RMVar_hsa_circ_85622,RMVar_hsa_circ_259555,RMVar_hsa_circ_259556,RMVar_hsa_circ_57457,RMVar_hsa_circ_259562,RMVar_hsa_circ_307616,RMVar_hsa_circ_121418,RMVar_hsa_circ_259558,RMVar_hsa_circ_359781,RMVar_hsa_circ_375763,RMVar_hsa_circ_82717,RMVar_hsa_circ_287271,RMVar_hsa_circ_259563,RMVar_hsa_circ_259560,RMVar_hsa_circ_259561,RMVar_hsa_circ_259559 48709 RMVar_ID_48709 Human_SNP_ID_415082345 A-to-I Human chr9 + 125212782 125212782 125212782 GTAAAATAACCCTGGGTTCAAGCGAGTCCCCTACCTCAGCCTCCCGAGTAGCTGGGACTACAGGC GTAAAATAACCCTGGGTTCAAGCGAGTCCCCTTCCTCAGCCTCCCGAGTAGCTGGGACTACAGGC A T RABEPK Ensembl:ENSG00000136933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1186894029 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24400,RMVar_hsa_circ_79833,RMVar_hsa_circ_85622,RMVar_hsa_circ_259555,RMVar_hsa_circ_259556,RMVar_hsa_circ_57457,RMVar_hsa_circ_259562,RMVar_hsa_circ_307616,RMVar_hsa_circ_121418,RMVar_hsa_circ_259558,RMVar_hsa_circ_359781,RMVar_hsa_circ_375763,RMVar_hsa_circ_82717,RMVar_hsa_circ_287271,RMVar_hsa_circ_259563,RMVar_hsa_circ_259560,RMVar_hsa_circ_259561,RMVar_hsa_circ_259559 48710 RMVar_ID_48710 Human_SNP_ID_415084471 A-to-I Human chr9 + 125220938 125220938 125220938 CCTGTAATCCCAGAGCTTTGGAAGGCTGAGGCAGGTGGACCGCTTAAGGTCAGGAGTTCGAGAAC CCTGTAATCCCAGAGCTTTGGAAGGCTGAGGCGGGTGGACCGCTTAAGGTCAGGAGTTCGAGAAC A G RABEPK Ensembl:ENSG00000136933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1021524704 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85622,RMVar_hsa_circ_259556,RMVar_hsa_circ_57457,RMVar_hsa_circ_259562,RMVar_hsa_circ_121418,RMVar_hsa_circ_259558,RMVar_hsa_circ_359781,RMVar_hsa_circ_375763,RMVar_hsa_circ_82717,RMVar_hsa_circ_259563,RMVar_hsa_circ_259561,RMVar_hsa_circ_290949,RMVar_hsa_circ_365757,RMVar_hsa_circ_318538,RMVar_hsa_circ_259564,RMVar_hsa_circ_344499,RMVar_hsa_circ_322545,RMVar_hsa_circ_259566 48711 RMVar_ID_48711 Human_SNP_ID_415084483 A-to-I Human chr9 + 125220957 125220957 125220957 GGAAGGCTGAGGCAGGTGGACCGCTTAAGGTCAGGAGTTCGAGAACAGCCTGGCCAACATACCTT GGAAGGCTGAGGCAGGTGGACCGCTTAAGGTCGGGAGTTCGAGAACAGCCTGGCCAACATACCTT A G RABEPK Ensembl:ENSG00000136933 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1158809880 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85622,RMVar_hsa_circ_259556,RMVar_hsa_circ_57457,RMVar_hsa_circ_259562,RMVar_hsa_circ_121418,RMVar_hsa_circ_259558,RMVar_hsa_circ_359781,RMVar_hsa_circ_375763,RMVar_hsa_circ_82717,RMVar_hsa_circ_259563,RMVar_hsa_circ_259561,RMVar_hsa_circ_290949,RMVar_hsa_circ_365757,RMVar_hsa_circ_318538,RMVar_hsa_circ_259564,RMVar_hsa_circ_344499,RMVar_hsa_circ_322545,RMVar_hsa_circ_259566 48712 RMVar_ID_48712 Human_SNP_ID_415084574 A-to-I Human chr9 + 125221296 125221296 125221296 AGGTGGGAGGATCACCTGAGGTCAGGAGTTTGAAACCAGCCTGGCCATCATGGCAAAACCCCATC AGGTGGGAGGATCACCTGAGGTCAGGAGTTTGGAACCAGCCTGGCCATCATGGCAAAACCCCATC A G RABEPK Ensembl:ENSG00000136933 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs192876193 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85622,RMVar_hsa_circ_259556,RMVar_hsa_circ_57457,RMVar_hsa_circ_259562,RMVar_hsa_circ_121418,RMVar_hsa_circ_259558,RMVar_hsa_circ_359781,RMVar_hsa_circ_375763,RMVar_hsa_circ_82717,RMVar_hsa_circ_259563,RMVar_hsa_circ_259561,RMVar_hsa_circ_290949,RMVar_hsa_circ_365757,RMVar_hsa_circ_318538,RMVar_hsa_circ_259564,RMVar_hsa_circ_344499,RMVar_hsa_circ_322545,RMVar_hsa_circ_259566 48713 RMVar_ID_48713 Human_SNP_ID_415084581 A-to-I Human chr9 + 125221326 125221326 125221326 TGAAACCAGCCTGGCCATCATGGCAAAACCCCATCTCTACTAAAAATACAAAAATTGGCCGGGTG TGAAACCAGCCTGGCCATCATGGCAAAACCCCGTCTCTACTAAAAATACAAAAATTGGCCGGGTG A G RABEPK Ensembl:ENSG00000136933 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1023725154 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_183098 RMVar_hsa_circ_85622,RMVar_hsa_circ_259556,RMVar_hsa_circ_57457,RMVar_hsa_circ_259562,RMVar_hsa_circ_121418,RMVar_hsa_circ_259558,RMVar_hsa_circ_359781,RMVar_hsa_circ_375763,RMVar_hsa_circ_82717,RMVar_hsa_circ_259563,RMVar_hsa_circ_259561,RMVar_hsa_circ_290949,RMVar_hsa_circ_365757,RMVar_hsa_circ_318538,RMVar_hsa_circ_259564,RMVar_hsa_circ_344499,RMVar_hsa_circ_322545,RMVar_hsa_circ_259566 48714 RMVar_ID_48714 Human_SNP_ID_415084759 A-to-I Human chr9 + 125221937 125221937 125221937 ACCTCAGGTAATCTGCCCACTTCAGCCTCCCAAAGTGCTGGGATTACAGGCTTGAGCCACTGCAC ACCTCAGGTAATCTGCCCACTTCAGCCTCCCAGAGTGCTGGGATTACAGGCTTGAGCCACTGCAC A G RABEPK Ensembl:ENSG00000136933 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs915510703 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85622,RMVar_hsa_circ_259556,RMVar_hsa_circ_57457,RMVar_hsa_circ_259562,RMVar_hsa_circ_121418,RMVar_hsa_circ_259558,RMVar_hsa_circ_359781,RMVar_hsa_circ_375763,RMVar_hsa_circ_82717,RMVar_hsa_circ_259563,RMVar_hsa_circ_259561,RMVar_hsa_circ_290949,RMVar_hsa_circ_365757,RMVar_hsa_circ_318538,RMVar_hsa_circ_259564,RMVar_hsa_circ_344499,RMVar_hsa_circ_322545,RMVar_hsa_circ_259566 48715 RMVar_ID_48715 Human_SNP_ID_415084770 A-to-I Human chr9 + 125221997 125221997 125221997 TGCACCCGGCCAGATTTTTGTATTTTTATTGTAGAGATGCAGTTTTGCCATGTTGCCCAGGCTGG TGCACCCGGCCAGATTTTTGTATTTTTATTGTGGAGATGCAGTTTTGCCATGTTGCCCAGGCTGG A G RABEPK Ensembl:ENSG00000136933 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1163284558 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85622,RMVar_hsa_circ_259556,RMVar_hsa_circ_57457,RMVar_hsa_circ_259562,RMVar_hsa_circ_121418,RMVar_hsa_circ_259558,RMVar_hsa_circ_359781,RMVar_hsa_circ_375763,RMVar_hsa_circ_82717,RMVar_hsa_circ_259563,RMVar_hsa_circ_259561,RMVar_hsa_circ_290949,RMVar_hsa_circ_365757,RMVar_hsa_circ_318538,RMVar_hsa_circ_259564,RMVar_hsa_circ_344499,RMVar_hsa_circ_322545,RMVar_hsa_circ_259566 48716 RMVar_ID_48716 Human_SNP_ID_415084897 A-to-I Human chr9 + 125222531 125222531 125222531 GGTCAGGAGTTCAAGAGCAGCCTGACCAACATAGTGAAACCTCGTTGCTACTAAAAATACAAAAA GGTCAGGAGTTCAAGAGCAGCCTGACCAACATGGTGAAACCTCGTTGCTACTAAAAATACAAAAA A G RABEPK Ensembl:ENSG00000136933 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs375332842 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85622,RMVar_hsa_circ_259556,RMVar_hsa_circ_57457,RMVar_hsa_circ_259562,RMVar_hsa_circ_121418,RMVar_hsa_circ_259558,RMVar_hsa_circ_359781,RMVar_hsa_circ_375763,RMVar_hsa_circ_82717,RMVar_hsa_circ_259563,RMVar_hsa_circ_259561,RMVar_hsa_circ_290949,RMVar_hsa_circ_365757,RMVar_hsa_circ_318538,RMVar_hsa_circ_259564,RMVar_hsa_circ_344499,RMVar_hsa_circ_322545,RMVar_hsa_circ_259566 48717 RMVar_ID_48717 Human_SNP_ID_415099425 A-to-I Human chr9 + 125275595 125275595 125275595 ACATGGCAAAACCCTGTTTCTGCAAAAAATACAAGAGTTAGTTGGGCATGGTGGCACATACGTGT ACATGGCAAAACCCTGTTTCTGCAAAAAATACGAGAGTTAGTTGGGCATGGTGGCACATACGTGT A G GAPVD1 Ensembl:ENSG00000165219 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1300612107 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83596,RMVar_hsa_circ_259570,RMVar_hsa_circ_339928,RMVar_hsa_circ_299137 48718 RMVar_ID_48718 Human_SNP_ID_415099426 A-to-I Human chr9 + 125275595 125275595 125275595 ACATGGCAAAACCCTGTTTCTGCAAAAAATACAAGAGTTAGTTGGGCATGGTGGCACATACGTGT ACATGGCAAAACCCTGTTTCTGCAAAAAATACTAGAGTTAGTTGGGCATGGTGGCACATACGTGT A T GAPVD1 Ensembl:ENSG00000165219 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1300612107 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83596,RMVar_hsa_circ_259570,RMVar_hsa_circ_339928,RMVar_hsa_circ_299137 48719 RMVar_ID_48719 Human_SNP_ID_415099738 A-to-I Human chr9 + 125276892 125276892 125276892 GCAGTGTTCTCATATCAGCCTCCTGAGAACCTAGGACTACAGGTGCATGCCACCACGCCTAGCTA GCAGTGTTCTCATATCAGCCTCCTGAGAACCTGGGACTACAGGTGCATGCCACCACGCCTAGCTA A G GAPVD1 Ensembl:ENSG00000165219 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs936731023 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83596,RMVar_hsa_circ_259570,RMVar_hsa_circ_339928,RMVar_hsa_circ_299137 48720 RMVar_ID_48720 Human_SNP_ID_415099749 A-to-I Human chr9 + 125276947 125276947 125276947 CGCCTAGCTAATTTTCTAAATTTTTTTTTCGTAAATATGGAGTCTCCCTATGTTGTCCAGGCTGG CGCCTAGCTAATTTTCTAAATTTTTTTTTCGTTAATATGGAGTCTCCCTATGTTGTCCAGGCTGG A T GAPVD1 Ensembl:ENSG00000165219 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1310922487 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83596,RMVar_hsa_circ_259570,RMVar_hsa_circ_339928,RMVar_hsa_circ_299137 48721 RMVar_ID_48721 Human_SNP_ID_415099935 A-to-I Human chr9 + 125277782 125277782 125277782 GCCTTGACCTCCCAGGCTCAAGCAGTCCTCCTACCTCAGCCTCCCAAGTACCTGGGACTTCAGGT GCCTTGACCTCCCAGGCTCAAGCAGTCCTCCTTCCTCAGCCTCCCAAGTACCTGGGACTTCAGGT A T GAPVD1 Ensembl:ENSG00000165219 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs927617840 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83596,RMVar_hsa_circ_259570,RMVar_hsa_circ_339928,RMVar_hsa_circ_299137 48722 RMVar_ID_48722 Human_SNP_ID_415107820 A-to-I Human chr9 + 125306838 125306838 125306838 CTATATCAGTACAAAAAGAGTTTAATTTTTTTAGGTTGGGTGCAGTGGCTCATGCTGGTAATCCT CTATATCAGTACAAAAAGAGTTTAATTTTTTTGGGTTGGGTGCAGTGGCTCATGCTGGTAATCCT A G GAPVD1 Ensembl:ENSG00000165219 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs376510269 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11269,RMVar_hsa_circ_83596,RMVar_hsa_circ_259570,RMVar_hsa_circ_328729,RMVar_hsa_circ_346251,RMVar_hsa_circ_374442,RMVar_hsa_circ_377716,RMVar_hsa_circ_338583,RMVar_hsa_circ_91090,RMVar_hsa_circ_259574,RMVar_hsa_circ_259576,RMVar_hsa_circ_259577,RMVar_hsa_circ_259575,RMVar_hsa_circ_259582,RMVar_hsa_circ_278396,RMVar_hsa_circ_369962,RMVar_hsa_circ_259573,RMVar_hsa_circ_352276,RMVar_hsa_circ_285406,RMVar_hsa_circ_72513,RMVar_hsa_circ_259583,RMVar_hsa_circ_259584,RMVar_hsa_circ_309116,RMVar_hsa_circ_377505,RMVar_hsa_circ_92938,RMVar_hsa_circ_259586 48723 RMVar_ID_48723 Human_SNP_ID_415110632 A-to-I Human chr9 + 125317564 125317564 125317564 GGAGAATCGCTTGAACTTGGGATGTAGAGGTTATGGTGAGCTGAGATTGTGCTGTTGTACTCCAG GGAGAATCGCTTGAACTTGGGATGTAGAGGTTTTGGTGAGCTGAGATTGTGCTGTTGTACTCCAG A T GAPVD1 Ensembl:ENSG00000165219 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1188318569 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11269,RMVar_hsa_circ_83596,RMVar_hsa_circ_259570,RMVar_hsa_circ_328729,RMVar_hsa_circ_374442,RMVar_hsa_circ_377716,RMVar_hsa_circ_91090,RMVar_hsa_circ_259574,RMVar_hsa_circ_259576,RMVar_hsa_circ_259575,RMVar_hsa_circ_369962,RMVar_hsa_circ_259573,RMVar_hsa_circ_285406,RMVar_hsa_circ_72513,RMVar_hsa_circ_259583,RMVar_hsa_circ_259584,RMVar_hsa_circ_92938,RMVar_hsa_circ_265017,RMVar_hsa_circ_259586,RMVar_hsa_circ_366252,RMVar_hsa_circ_322136,RMVar_hsa_circ_265241,RMVar_hsa_circ_259587,RMVar_hsa_circ_259589,RMVar_hsa_circ_122103,RMVar_hsa_circ_13501,RMVar_hsa_circ_41753,RMVar_hsa_circ_48482,RMVar_hsa_circ_32775 48724 RMVar_ID_48724 Human_SNP_ID_415120668 A-to-I Human chr9 + 125356858 125356858 125356858 CATGCCCTGCTAATTTTTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGG CATGCCCTGCTAATTTTTTTTGTATTTTTAGTGGAGATGGGGTTTCACCATGTTGGCCAGGCTGG A G GAPVD1 Ensembl:ENSG00000165219 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs994252512 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265241,RMVar_hsa_circ_81027,RMVar_hsa_circ_259610,RMVar_hsa_circ_84480,RMVar_hsa_circ_259613,RMVar_hsa_circ_259619,RMVar_hsa_circ_305058,RMVar_hsa_circ_259618 48725 RMVar_ID_48725 Human_SNP_ID_415121669 A-to-I Human chr9 + 125361121 125361121 125361121 CTCCAGCTGGCCTCAAGTGATTCGCCCGCCTCAGCCTCCTGAAGTGTTGGGATCATAGACATGAG CTCCAGCTGGCCTCAAGTGATTCGCCCGCCTCGGCCTCCTGAAGTGTTGGGATCATAGACATGAG A G GAPVD1 Ensembl:ENSG00000165219 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1259575929 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265241,RMVar_hsa_circ_84480,RMVar_hsa_circ_259613,RMVar_hsa_circ_259619,RMVar_hsa_circ_100797,RMVar_hsa_circ_259620 48726 RMVar_ID_48726 Human_SNP_ID_415150824 A-to-I Human chr9 - 125478557 125478557 125478557 GGGAGGCCAAGGTGGGAGGATTGCTAGAAGCCAGGAATTCAAGACCAGTCTGGACAACATGACAA GGGAGGCCAAGGTGGGAGGATTGCTAGAAGCCGGGAATTCAAGACCAGTCTGGACAACATGACAA T C MAPKAP1 Ensembl:ENSG00000119487 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1283355978 Functional Loss SNV dbSNP153 33..33 33 - - - 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_291451,RMVar_hsa_circ_259624,RMVar_hsa_circ_259623,RMVar_hsa_circ_259626,RMVar_hsa_circ_320616 48727 RMVar_ID_48727 Human_SNP_ID_415151619 A-to-I Human chr9 - 125481561 125481561 125481561 AAAAATAGCCAGGTGTGGTGGTGCCTGCCTGTAGTCCCAGCTACTCAGGAGGCTGCGATGGGAGG AAAAATAGCCAGGTGTGGTGGTGCCTGCCTGTCGTCCCAGCTACTCAGGAGGCTGCGATGGGAGG T G MAPKAP1 Ensembl:ENSG00000119487 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1376823832 Functional Loss SNV dbSNP153 33..33 33 - - - 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_291451,RMVar_hsa_circ_259624,RMVar_hsa_circ_259623,RMVar_hsa_circ_259626,RMVar_hsa_circ_320616 48728 RMVar_ID_48728 Human_SNP_ID_415156685 A-to-I Human chr9 - 125503746 125503746 125503746 TGCCACTGCACTCCAGCCTGGGTGACAGAGTGAGATTCCGTCTCAAAAAAAAAAGAAAGAAAGAA TGCCACTGCACTCCAGCCTGGGTGACAGAGTGCGATTCCGTCTCAAAAAAAAAAGAAAGAAAGAA T G MAPKAP1 Ensembl:ENSG00000119487 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1169966169 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_259627 48729 RMVar_ID_48729 Human_SNP_ID_415156934 A-to-I Human chr9 - 125504626 125504620 125504626 ACCACCCCTGGCTAATTTTTATTTTTATTTTTATTTTTTATTTTTAGTAGAGGTGGAGTTTTGCT ACCACCCCTGGCTAATTTTTATTTTTATTTTT______TATTTTTAGTAGAGGTGGAGTTTTGCT AAAAAAT A MAPKAP1 Ensembl:ENSG00000119487 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1193511085 Functional Loss DEL dbSNP153 33..38 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_259627 48730 RMVar_ID_48730 Human_SNP_ID_415156936 A-to-I Human chr9 - 125504626 125504626 125504626 ACCACCCCTGGCTAATTTTTATTTTTATTTTTATTTTTTATTTTTAGTAGAGGTGGAGTTTTGCT ACCACCCCTGGCTAATTTTTATTTTTATTTTTGTTTTTTATTTTTAGTAGAGGTGGAGTTTTGCT T C MAPKAP1 Ensembl:ENSG00000119487 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs753831957 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_259627 48731 RMVar_ID_48731 Human_SNP_ID_415159235 A-to-I Human chr9 - 125514581 125514581 125514581 TTGCTTTTAAGCTATAGGCAGCATTTAAGATTAGAGACTTGCTCGGCAGCCAGGATTCACAGTTC TTGCTTTTAAGCTATAGGCAGCATTTAAGATTGGAGACTTGCTCGGCAGCCAGGATTCACAGTTC T C MAPKAP1 Ensembl:ENSG00000119487 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1376155914 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6923,RMVar_hsa_circ_98768,RMVar_hsa_circ_259622,RMVar_hsa_circ_259621,RMVar_hsa_circ_326603,RMVar_hsa_circ_318116,RMVar_hsa_circ_13987,RMVar_hsa_circ_74177,RMVar_hsa_circ_53189,RMVar_hsa_circ_50116,RMVar_hsa_circ_82712,RMVar_hsa_circ_308672,RMVar_hsa_circ_259628,RMVar_hsa_circ_347293,RMVar_hsa_circ_8718,RMVar_hsa_circ_48010 48732 RMVar_ID_48732 Human_SNP_ID_415162128 A-to-I Human chr9 - 125526974 125526974 125526974 GGTCAGGAGATCGAGACTATCCTGGCTAACACAGTGAAACCCTACCTCTATTAAAAATACAAAAA GGTCAGGAGATCGAGACTATCCTGGCTAACACGGTGAAACCCTACCTCTATTAAAAATACAAAAA T C MAPKAP1 Ensembl:ENSG00000119487 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1276811506 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6923,RMVar_hsa_circ_98768,RMVar_hsa_circ_259622,RMVar_hsa_circ_259621,RMVar_hsa_circ_326603,RMVar_hsa_circ_318116,RMVar_hsa_circ_13987,RMVar_hsa_circ_74177,RMVar_hsa_circ_53189,RMVar_hsa_circ_50116,RMVar_hsa_circ_82712,RMVar_hsa_circ_308672,RMVar_hsa_circ_259628,RMVar_hsa_circ_347293,RMVar_hsa_circ_8718,RMVar_hsa_circ_48010 48733 RMVar_ID_48733 Human_SNP_ID_415176177 A-to-I Human chr9 - 125585580 125585580 125585580 ACCTGATCGGGCTCATCTGCTGGCAGTATACAAGCGAAGGACGGGAGCCGAAGCTCAAGTAATCC ACCTGATCGGGCTCATCTGCTGGCAGTATACAGGCGAAGGACGGGAGCCGAAGCTCAAGTAATCC T C MAPKAP1 Ensembl:ENSG00000119487 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs781541256 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5633621,Human_RBP_ID_9408538,Human_RBP_ID_18129660,Human_RBP_ID_27783103 Human_Splice_Rec_1080669,Human_Splice_Rec_1080687,Human_Splice_Rec_1080709,Human_Splice_Rec_1080729,Human_Splice_Rec_1080749,Human_Splice_Rec_1080767,Human_Splice_Rec_1080793,Human_Splice_Rec_1080827,Human_Splice_Rec_1080839,Human_Splice_Rec_1080853,Human_Splice_Rec_1080863,Human_Splice_Rec_1080867,Human_Splice_Rec_1080873,Human_Splice_Rec_1080879 Human_miRNA_ID_1967203,Human_miRNA_ID_1967204 RMVar_hsa_circ_6923,RMVar_hsa_circ_98768,RMVar_hsa_circ_259621,RMVar_hsa_circ_326603,RMVar_hsa_circ_74177,RMVar_hsa_circ_50116,RMVar_hsa_circ_82712,RMVar_hsa_circ_259628,RMVar_hsa_circ_347293,RMVar_hsa_circ_8718,RMVar_hsa_circ_298638,RMVar_hsa_circ_311986,RMVar_hsa_circ_259632,RMVar_hsa_circ_3770,RMVar_hsa_circ_326246,RMVar_hsa_circ_309026,RMVar_hsa_circ_259635,RMVar_hsa_circ_259636,RMVar_hsa_circ_305703,RMVar_hsa_circ_375841,RMVar_hsa_circ_259637 48734 RMVar_ID_48734 Human_SNP_ID_415184904 A-to-I Human chr9 - 125622583 125622583 125622583 AAATTAGCCAGGCATGGTGGTGCCCGCCTGCAATCCTAGCTACTCAGGAGGCTGAGGCAGGAGAA AAATTAGCCAGGCATGGTGGTGCCCGCCTGCAGTCCTAGCTACTCAGGAGGCTGAGGCAGGAGAA T C MAPKAP1 Ensembl:ENSG00000119487 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs898140217 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74177,RMVar_hsa_circ_50116,RMVar_hsa_circ_82712,RMVar_hsa_circ_259628,RMVar_hsa_circ_8718,RMVar_hsa_circ_311986,RMVar_hsa_circ_3770,RMVar_hsa_circ_326246,RMVar_hsa_circ_259636,RMVar_hsa_circ_305703,RMVar_hsa_circ_375841,RMVar_hsa_circ_259637 48735 RMVar_ID_48735 Human_SNP_ID_415188954 A-to-I Human chr9 - 125638030 125638030 125638030 TGGGGGCTCAGACCTGTAATCCCAGCACTTCAAGAGGCCAAGACTGGTAGATCACCTGAGGTCAG TGGGGGCTCAGACCTGTAATCCCAGCACTTCAGGAGGCCAAGACTGGTAGATCACCTGAGGTCAG T C MAPKAP1 Ensembl:ENSG00000119487 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1324313585 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74177,RMVar_hsa_circ_50116,RMVar_hsa_circ_82712,RMVar_hsa_circ_259628,RMVar_hsa_circ_8718,RMVar_hsa_circ_311986,RMVar_hsa_circ_3770,RMVar_hsa_circ_326246,RMVar_hsa_circ_259636,RMVar_hsa_circ_305703,RMVar_hsa_circ_375841,RMVar_hsa_circ_259637 48736 RMVar_ID_48736 Human_SNP_ID_415192099 A-to-I Human chr9 - 125651121 125651121 125651121 CTGGTATATAGTATAGAAGGATCGCCGGGCACAGTGGCTCATGCCTGTAACCCCAGCATGTTGGG CTGGTATATAGTATAGAAGGATCGCCGGGCACTGTGGCTCATGCCTGTAACCCCAGCATGTTGGG T A MAPKAP1 Ensembl:ENSG00000119487 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1384870201 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16575821 RMVar_hsa_circ_74177,RMVar_hsa_circ_50116,RMVar_hsa_circ_8718,RMVar_hsa_circ_311986,RMVar_hsa_circ_3770,RMVar_hsa_circ_326246,RMVar_hsa_circ_259636,RMVar_hsa_circ_305703,RMVar_hsa_circ_375841,RMVar_hsa_circ_259637,RMVar_hsa_circ_259638 48737 RMVar_ID_48737 Human_SNP_ID_415197347 A-to-I Human chr9 - 125673364 125673364 125673364 AAATTAGCTGGGCATGGTGGCGCATCCCTGTAATCCCAGCTACGCGGGAGGCTGAGGCCGGAGAA AAATTAGCTGGGCATGGTGGCGCATCCCTGTATTCCCAGCTACGCGGGAGGCTGAGGCCGGAGAA T A MAPKAP1 Ensembl:ENSG00000119487 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs961133985 Functional Loss SNV dbSNP153 33..33 33 - - - 48738 RMVar_ID_48738 Human_SNP_ID_415197433 A-to-I Human chr9 - 125673749 125673749 125673749 TAATTATTATATATATATATTTTTGTAGAGATAGAGTTTTGATTGTGTTGCCCATGTTGGTCTTG TAATTATTATATATATATATTTTTGTAGAGATGGAGTTTTGATTGTGTTGCCCATGTTGGTCTTG T C MAPKAP1 Ensembl:ENSG00000119487 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1399197761 Functional Loss SNV dbSNP153 33..33 33 - - - 48739 RMVar_ID_48739 Human_SNP_ID_415203638 A-to-I Human chr9 - 125696316 125696316 125696316 GCCTCAACTTCCTGGACTCAAGCGATCCTCCCACCTCTTCCTCCCCAGCAGCTGGGACTACAGGC GCCTCAACTTCCTGGACTCAAGCGATCCTCCCTCCTCTTCCTCCCCAGCAGCTGGGACTACAGGC T A MAPKAP1 Ensembl:ENSG00000119487 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1190039566 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1080888,Human_Splice_Rec_1080889 48740 RMVar_ID_48740 Human_SNP_ID_415231034 A-to-I Human chr9 + 125800882 125800882 125800882 TCAAGCGATTCTCCTACCTCAGTGTCTCCAGTAACTGGGATTACAGGCGCCTGCCACCATGCCTG TCAAGCGATTCTCCTACCTCAGTGTCTCCAGTTACTGGGATTACAGGCGCCTGCCACCATGCCTG A T PBX3 Ensembl:ENSG00000167081 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1191549834 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1668,RMVar_hsa_circ_332436,RMVar_hsa_circ_65148,RMVar_hsa_circ_259647 48741 RMVar_ID_48741 Human_SNP_ID_415231527 A-to-I Human chr9 + 125802589 125802589 125802589 CAGGGTTTCACTATGTTGTCCAGGCTGGTCTCAAACTCCTGGGTTCAAGCCATCCGCCTGCTCAG CAGGGTTTCACTATGTTGTCCAGGCTGGTCTCGAACTCCTGGGTTCAAGCCATCCGCCTGCTCAG A G PBX3 Ensembl:ENSG00000167081 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs925645783 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1668,RMVar_hsa_circ_332436,RMVar_hsa_circ_65148,RMVar_hsa_circ_259647 48742 RMVar_ID_48742 Human_SNP_ID_415480573 A-to-I Human chr9 + 126810768 126810768 126810768 CTGGTGATCCGCCCGCCTCGGCCTCCCAAAGTACTGGGATTACAGGAGTGAGCCACCATGCCTGG CTGGTGATCCGCCCGCCTCGGCCTCCCAAAGTCCTGGGATTACAGGAGTGAGCCACCATGCCTGG A C ZBTB43 Ensembl:ENSG00000169155 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs953721693 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86012,RMVar_hsa_circ_259675 48743 RMVar_ID_48743 Human_SNP_ID_415481218 A-to-I Human chr9 + 126813253 126813253 126813253 CCACGTGCCTCAGCCTCCCAAAATGCTGGGATAAAAGACGTGAGCCACCATGCCTGGCCCCACTG CCACGTGCCTCAGCCTCCCAAAATGCTGGGATGAAAGACGTGAGCCACCATGCCTGGCCCCACTG A G ZBTB43 Ensembl:ENSG00000169155 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1029179022 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16578933 RMVar_hsa_circ_86012,RMVar_hsa_circ_259675 48744 RMVar_ID_48744 Human_SNP_ID_415481478 A-to-I Human chr9 + 126814294 126814265 126814295 CCTGATTTTTACAGATGAAATTTACATCTGTAAAATTTTTACAGATGAAATTTACATCTGTAAAA CCTG______________________________ATTTTTACAGATGAAATTTACATCTGTAAAA GATTTTTACAGATGAAATTTACATCTGTAAA G ZBTB43 Ensembl:ENSG00000169155 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs71377973 Functional Loss DEL dbSNP153 5..34 33 - - - RMVar_hsa_circ_86012,RMVar_hsa_circ_259675 48745 RMVar_ID_48745 Human_SNP_ID_415481478 A-to-I Human chr9 + 126814295 126814265 126814295 CTGATTTTTACAGATGAAATTTACATCTGTAAAATTTTTACAGATGAAATTTACATCTGTAAAAT CTG______________________________ATTTTTACAGATGAAATTTACATCTGTAAAAT GATTTTTACAGATGAAATTTACATCTGTAAA G ZBTB43 Ensembl:ENSG00000169155 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs71377973 Functional Loss DEL dbSNP153 4..33 33 - - - RMVar_hsa_circ_86012,RMVar_hsa_circ_259675 48746 RMVar_ID_48746 Human_SNP_ID_415481498 A-to-I Human chr9 + 126814294 126814294 126814294 CCTGATTTTTACAGATGAAATTTACATCTGTAAAATTTTTACAGATGAAATTTACATCTGTAAAA CCTGATTTTTACAGATGAAATTTACATCTGTAGAATTTTTACAGATGAAATTTACATCTGTAAAA A G ZBTB43 Ensembl:ENSG00000169155 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1182706955 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86012,RMVar_hsa_circ_259675 48747 RMVar_ID_48747 Human_SNP_ID_415481501 A-to-I Human chr9 + 126814302 126814301 126814303 TTACAGATGAAATTTACATCTGTAAAATTTTTACAGATGAAATTTACATCTGTAAAATGTAAATT TTACAGATGAAATTTACATCTGTAAAATTTTT__AGATGAAATTTACATCTGTAAAATGTAAATT TAC T ZBTB43 Ensembl:ENSG00000169155 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1271885194 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_86012,RMVar_hsa_circ_259675 48748 RMVar_ID_48748 Human_SNP_ID_415482752 A-to-I Human chr9 + 126818323 126818323 126818323 TAAAAAATATATATATATATATATTTAGAAACAAGGTCTTGCTGTGTCGTCCAGGCTGGACTCAA TAAAAAATATATATATATATATATTTAGAAACGAGGTCTTGCTGTGTCGTCCAGGCTGGACTCAA A G ZBTB43 Ensembl:ENSG00000169155 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1387496516 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16579017 RMVar_hsa_circ_86012,RMVar_hsa_circ_259675 48749 RMVar_ID_48749 Human_SNP_ID_415485956 A-to-I Human chr9 + 126830511 126830511 126830511 TGCAAAAAATACAAAAATTAGCCGGATGTGGTAGTAGTGCATGCCTGAAGTCCCAGCTACTCAGG TGCAAAAAATACAAAAATTAGCCGGATGTGGTCGTAGTGCATGCCTGAAGTCCCAGCTACTCAGG A C ZBTB43 Ensembl:ENSG00000169155 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs944257838 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16579170 RMVar_hsa_circ_86012,RMVar_hsa_circ_259675 48750 RMVar_ID_48750 Human_SNP_ID_415485975 A-to-I Human chr9 + 126830603 126830603 126830603 CCAGGAGTTTGAGACTGCAGTGAGCTGTGATCACACCACTGTACTCCAGCCTGGGTGACAAGAGT CCAGGAGTTTGAGACTGCAGTGAGCTGTGATCGCACCACTGTACTCCAGCCTGGGTGACAAGAGT A G ZBTB43 Ensembl:ENSG00000169155 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1349730098 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86012,RMVar_hsa_circ_259675 48751 RMVar_ID_48751 Human_SNP_ID_415570877 A-to-I Human chr9 + 127183812 127183812 127183812 TGGGAGGGGCCCTCCATGAGGACCTCAGGGATAGGAGGCCAGTTGTGGCCCATTACTCTGGGATT TGGGAGGGGCCCTCCATGAGGACCTCAGGGATCGGAGGCCAGTTGTGGCCCATTACTCTGGGATT A C RALGPS1 Ensembl:ENSG00000136828 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs761993057 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126969,RMVar_hsa_circ_108703,RMVar_hsa_circ_259684,RMVar_hsa_circ_259691,RMVar_hsa_circ_267293 48752 RMVar_ID_48752 Human_SNP_ID_415570878 A-to-I Human chr9 + 127183812 127183812 127183812 TGGGAGGGGCCCTCCATGAGGACCTCAGGGATAGGAGGCCAGTTGTGGCCCATTACTCTGGGATT TGGGAGGGGCCCTCCATGAGGACCTCAGGGATGGGAGGCCAGTTGTGGCCCATTACTCTGGGATT A G RALGPS1 Ensembl:ENSG00000136828 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs761993057 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126969,RMVar_hsa_circ_108703,RMVar_hsa_circ_259684,RMVar_hsa_circ_259691,RMVar_hsa_circ_267293 48753 RMVar_ID_48753 Human_SNP_ID_415570879 A-to-I Human chr9 + 127183812 127183812 127183812 TGGGAGGGGCCCTCCATGAGGACCTCAGGGATAGGAGGCCAGTTGTGGCCCATTACTCTGGGATT TGGGAGGGGCCCTCCATGAGGACCTCAGGGATTGGAGGCCAGTTGTGGCCCATTACTCTGGGATT A T RALGPS1 Ensembl:ENSG00000136828 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs761993057 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126969,RMVar_hsa_circ_108703,RMVar_hsa_circ_259684,RMVar_hsa_circ_259691,RMVar_hsa_circ_267293 48754 RMVar_ID_48754 Human_SNP_ID_415621076 A-to-I Human chr9 + 127400368 127400368 127400368 TTTGGTAGAAAGGGGGTTTCACCGTGTTAGCCAGGATGGTCTTGATCTCCTGACCTCATGAACCG TTTGGTAGAAAGGGGGTTTCACCGTGTTAGCCGGGATGGTCTTGATCTCCTGACCTCATGAACCG A G SLC2A8 Ensembl:ENSG00000136856 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs570664041 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_259728 48755 RMVar_ID_48755 Human_SNP_ID_415621087 A-to-I Human chr9 - 127400413 127400413 127400413 TGGCTCACACCTGTAATCCCAGCACTTTGGGAAGCTGAGGTTTGGCGGTTCATGAGGTCAGGAGA TGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGTTTGGCGGTTCATGAGGTCAGGAGA T C RF00017-4490,RF00017-4541,RF00017-4552 RNACentral:URS0000922AF7,RNACentral:URS0000992647,RNACentral:URS0000973F83 SRP RNA,SRP RNA,SRP RNA intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1369853780 Functional Loss SNV dbSNP153 33..33 33 - - - 48756 RMVar_ID_48756 Human_SNP_ID_415627299 A-to-I Human chr9 - 127421646 127421646 127421646 GGAATGCTGAGGCAGGTGCATCACCTGAGGTCAGGAGTTTGAGACCAGCCTGGCCAACATGGTGA GGAATGCTGAGGCAGGTGCATCACCTGAGGTCCGGAGTTTGAGACCAGCCTGGCCAACATGGTGA T G lnc-RPL12-1,RF00017-4490,RF00017-4541,lnc-RPL12-1:2,RF00017-4552 RNACentral:URS0000D57646,RNACentral:URS0000922AF7,RNACentral:URS0000992647,RNACentral:URS0000D5DA56,RNACentral:URS0000973F83 lincRNA,SRP RNA,SRP RNA,lincRNA,SRP RNA intron,intron,intron,exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1406839825 Functional Loss SNV dbSNP153 33..33 33 - - - 48757 RMVar_ID_48757 Human_SNP_ID_415633804 A-to-I Human chr9 + 127446438 127446438 127446438 GCTTGCTGAAGTCTCCACTCCTGCACCCTCCTACCTCAGCATCCTAAGTAGCCAGGCACACACAC GCTTGCTGAAGTCTCCACTCCTGCACCCTCCTGCCTCAGCATCCTAAGTAGCCAGGCACACACAC A G RF00017-4506,RF00017-1003,RF00017-4495 RNACentral:URS000096AE3B,RNACentral:URS0000945854,RNACentral:URS0000923EDC SRP RNA,SRP RNA,SRP RNA intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1289028818 Functional Loss SNV dbSNP153 33..33 33 - - - 48758 RMVar_ID_48758 Human_SNP_ID_415635477 A-to-I Human chr9 - 127451121 127451121 127451121 GCCCCGGCCAAGCCTCAGCCTTTCTGGGCCTTAGCTTCTTCACGTGTAGGTGGGGAGGGAGGACT GCCCCGGCCAAGCCTCAGCCTTTCTGGGCCTTCGCTTCTTCACGTGTAGGTGGGGAGGGAGGACT T G RPL12 Ensembl:ENSG00000197958 Protein coding exon GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1482538298 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_92078,Human_RBP_ID_712142,Human_RBP_ID_16580719,Human_RBP_ID_22690233,Human_RBP_ID_22747791 Human_Splice_Rec_1081959 RMVar_hsa_circ_83916,RMVar_hsa_circ_259748 48759 RMVar_ID_48759 Human_SNP_ID_415639911 A-to-I Human chr9 + 127466828 127466828 127466828 CAAGACTTTGAGACTAGCCTGGGTAACATAGTAGGACTTTATCTCTACAAAAAATACAAAAATTA CAAGACTTTGAGACTAGCCTGGGTAACATAGTGGGACTTTATCTCTACAAAAAATACAAAAATTA A G LRSAM1 Ensembl:ENSG00000148356 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1314080021 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9925,RMVar_hsa_circ_272797,RMVar_hsa_circ_121391,RMVar_hsa_circ_30622,RMVar_hsa_circ_333222,RMVar_hsa_circ_45034,RMVar_hsa_circ_259753 48760 RMVar_ID_48760 Human_SNP_ID_415642588 A-to-I Human chr9 + 127476929 127476929 127476929 GAACTCCTGAACTCAAGTGATCCACTTGTCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAG GAACTCCTGAACTCAAGTGATCCACTTGTCTCCGCCTCCCAAAGTGCTGGGATTACAGGCATGAG A C LRSAM1 Ensembl:ENSG00000148356 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1055128257 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121391,RMVar_hsa_circ_30622,RMVar_hsa_circ_45034,RMVar_hsa_circ_13371,RMVar_hsa_circ_259753 48761 RMVar_ID_48761 Human_SNP_ID_415642589 A-to-I Human chr9 + 127476929 127476929 127476929 GAACTCCTGAACTCAAGTGATCCACTTGTCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAG GAACTCCTGAACTCAAGTGATCCACTTGTCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAG A G LRSAM1 Ensembl:ENSG00000148356 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1055128257 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121391,RMVar_hsa_circ_30622,RMVar_hsa_circ_45034,RMVar_hsa_circ_13371,RMVar_hsa_circ_259753 48762 RMVar_ID_48762 Human_SNP_ID_415653615 A-to-I Human chr9 - 127516943 127516934 127516943 GCGCTTCGAGGAGGTGCTGTCCAAGGTGCAGCAGGTGCAGCCGGCCATGCAGGCCGTCATCCGAA GCGCTTCGAGGAGGTGCTGTCCAAGGTGCAGC_________CGGCCATGCAGGCCGTCATCCGAA GGCTGCACCT G NIBAN2 Ensembl:ENSG00000136830 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1225615142 Functional Loss DEL dbSNP153 33..41 33 - - - Human_RBP_ID_91149,Human_RBP_ID_8696974 Human_Splice_Rec_1082278,Human_Splice_Rec_1082279,Human_Splice_Rec_1082308,Human_Splice_Rec_1082309,Human_Splice_Rec_1082337 Human_miRNA_ID_2511816,Human_miRNA_ID_2750594,Human_miRNA_ID_3054635 RMVar_hsa_circ_117797,RMVar_hsa_circ_108141,RMVar_hsa_circ_259760,RMVar_hsa_circ_259764,RMVar_hsa_circ_98591,RMVar_hsa_circ_101103,RMVar_hsa_circ_259765,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_48174,RMVar_hsa_circ_259771,RMVar_hsa_circ_259772,RMVar_hsa_circ_308178,RMVar_hsa_circ_357415,RMVar_hsa_circ_52596 48763 RMVar_ID_48763 Human_SNP_ID_415655592 A-to-I Human chr9 - 127523729 127523729 127523729 CTACTACTTCTGCATGATGACAGAAGCCGAGCAGGACAAGTGGCAGGCTGTGCTGCAGGACTGCA CTACTACTTCTGCATGATGACAGAAGCCGAGCGGGACAAGTGGCAGGCTGTGCTGCAGGACTGCA T C NIBAN2 Ensembl:ENSG00000136830 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1369443647 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22467075,Human_RBP_ID_26833555 Human_Splice_Rec_1082273,Human_Splice_Rec_1082303 Human_miRNA_ID_2254775 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 48764 RMVar_ID_48764 Human_SNP_ID_415655597 A-to-I Human chr9 - 127523737 127523737 127523737 GCGCGTCACTACTACTTCTGCATGATGACAGAAGCCGAGCAGGACAAGTGGCAGGCTGTGCTGCA GCGCGTCACTACTACTTCTGCATGATGACAGAGGCCGAGCAGGACAAGTGGCAGGCTGTGCTGCA T C NIBAN2 Ensembl:ENSG00000136830 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1419852060 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22467075,Human_RBP_ID_26833555 Human_Splice_Rec_1082273,Human_Splice_Rec_1082303 Human_miRNA_ID_2254775 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 48765 RMVar_ID_48765 Human_SNP_ID_415665600 A-to-I Human chr9 - 127563687 127563687 127563687 ACATGATGAAACCACGTCTCTACTAAAAAATTAGCCGGGCCTGGTGGTGCGTGCCTGTAGTCCCA ACATGATGAAACCACGTCTCTACTAAAAAATTGGCCGGGCCTGGTGGTGCGTGCCTGTAGTCCCA T C NIBAN2 Ensembl:ENSG00000136830 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1016288930 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108141,RMVar_hsa_circ_259765,RMVar_hsa_circ_90935,RMVar_hsa_circ_259778 48766 RMVar_ID_48766 Human_SNP_ID_415670604 A-to-I Human chr9 + 127583006 127583006 127583006 AAGTTTTTTATTTTTTGTACAGACAGGGTCTCACTATGTTGTCCAGTCTTGAACTCCTGGGCTTA AAGTTTTTTATTTTTTGTACAGACAGGGTCTCCCTATGTTGTCCAGTCTTGAACTCCTGGGCTTA A C STXBP1 Ensembl:ENSG00000136854 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs771873752 Functional Loss SNV dbSNP153 33..33 33 - - - 48767 RMVar_ID_48767 Human_SNP_ID_415688804 A-to-I Human chr9 + 127657890 127657890 127657890 TGTTTTTGTCGTTGTTTTTGAGATGGAGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGTACT TGTTTTTGTCGTTGTTTTTGAGATGGAGTCTCCCTCTGTCACCCAGGCTGGAGTGCAGTGGTACT A C STXBP1 Ensembl:ENSG00000136854 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 29129909,30559470 RNA-Seq:(High) rs1186672914 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15569,RMVar_hsa_circ_18897,RMVar_hsa_circ_120746,RMVar_hsa_circ_259779,RMVar_hsa_circ_108386,RMVar_hsa_circ_17293,RMVar_hsa_circ_259780 48768 RMVar_ID_48768 Human_SNP_ID_415724485 A-to-I Human chr9 + 127790866 127790866 127790866 CAGGCTGAAGTGCAGTGGTGAGATCTCGGCTCACTGCGACTTCTGCCTCCCGGGTTCAAGTGATT CAGGCTGAAGTGCAGTGGTGAGATCTCGGCTCGCTGCGACTTCTGCCTCCCGGGTTCAAGTGATT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs997059444 Functional Loss SNV dbSNP153 33..33 33 - - - 48769 RMVar_ID_48769 Human_SNP_ID_415724500 A-to-I Human chr9 + 127790891 127790891 127790891 TCGGCTCACTGCGACTTCTGCCTCCCGGGTTCAAGTGATTCTCCTGTCTCAGCCTCCTGAGTAGC TCGGCTCACTGCGACTTCTGCCTCCCGGGTTCGAGTGATTCTCCTGTCTCAGCCTCCTGAGTAGC A G - - Other Unknown GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank - 29129909,30559470 RNA-Seq:(High) rs901773773 Functional Loss SNV dbSNP153 33..33 33 - - - 48770 RMVar_ID_48770 Human_SNP_ID_415724502 A-to-I Human chr9 + 127790896 127790896 127790896 TCACTGCGACTTCTGCCTCCCGGGTTCAAGTGATTCTCCTGTCTCAGCCTCCTGAGTAGCTGGGA TCACTGCGACTTCTGCCTCCCGGGTTCAAGTGCTTCTCCTGTCTCAGCCTCCTGAGTAGCTGGGA A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1015992217 Functional Loss SNV dbSNP153 33..33 33 - - - 48771 RMVar_ID_48771 Human_SNP_ID_415724804 A-to-I Human chr9 + 127791852 127791851 127791852 TAAATCCAAATTGGCCAGGCGCAGCGGCTCACACCTATAATCCCAGCACTTCGGGAGGCCAAGGC TAAATCCAAATTGGCCAGGCGCAGCGGCTCAC_CCTATAATCCCAGCACTTCGGGAGGCCAAGGC CA C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1209793275 Functional Loss DEL dbSNP153 33..33 33 - - - 48772 RMVar_ID_48772 Human_SNP_ID_415724806 A-to-I Human chr9 + 127791856 127791856 127791856 TCCAAATTGGCCAGGCGCAGCGGCTCACACCTATAATCCCAGCACTTCGGGAGGCCAAGGCGGGC TCCAAATTGGCCAGGCGCAGCGGCTCACACCTTTAATCCCAGCACTTCGGGAGGCCAAGGCGGGC A T - - Other Unknown GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1451371173 Functional Loss SNV dbSNP153 33..33 33 - - - 48773 RMVar_ID_48773 Human_SNP_ID_415724819 A-to-I Human chr9 + 127791880 127791880 127791880 TCACACCTATAATCCCAGCACTTCGGGAGGCCAAGGCGGGCGGATCACGAGGTCAGGAGTCGGAG TCACACCTATAATCCCAGCACTTCGGGAGGCCCAGGCGGGCGGATCACGAGGTCAGGAGTCGGAG A C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1000072337 Functional Loss SNV dbSNP153 33..33 33 - - - 48774 RMVar_ID_48774 Human_SNP_ID_415724820 A-to-I Human chr9 + 127791880 127791880 127791880 TCACACCTATAATCCCAGCACTTCGGGAGGCCAAGGCGGGCGGATCACGAGGTCAGGAGTCGGAG TCACACCTATAATCCCAGCACTTCGGGAGGCCGAGGCGGGCGGATCACGAGGTCAGGAGTCGGAG A G - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1000072337 Functional Loss SNV dbSNP153 33..33 33 - - - 48775 RMVar_ID_48775 Human_SNP_ID_415724892 A-to-I Human chr9 + 127792057 127792057 127792057 TCCCAGGTACATGCCTGTAGTCCCAGCTGCTCAGGAGGCTGAGGCAGGAGAATCACTTGAACTAG TCCCAGGTACATGCCTGTAGTCCCAGCTGCTCGGGAGGCTGAGGCAGGAGAATCACTTGAACTAG A G - - Other Unknown GSE38233;GSE107867 cultured B-cells;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 24183664,30559470 RNA-Seq:(High) rs1219518329 Functional Loss SNV dbSNP153 33..33 33 - - - 48776 RMVar_ID_48776 Human_SNP_ID_415724989 A-to-I Human chr9 + 127792385 127792384 127792385 GAGAGGCAGAGGTGGGAGAATCGCTTGAACCCAGGAGGCAAGAGATTGCAGTAAGCTGAGATGAC GAGAGGCAGAGGTGGGAGAATCGCTTGAACCC_GGAGGCAAGAGATTGCAGTAAGCTGAGATGAC CA C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1402829187 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_18130088 48777 RMVar_ID_48777 Human_SNP_ID_415725539 A-to-I Human chr9 + 127793918 127793918 127793918 TCAGTATAATTTTTATTTTATTATTTTTTTTTAAGACAGAGTCTGGCTCTGTCGCCCAGGCTGGA TCAGTATAATTTTTATTTTATTATTTTTTTTTGAGACAGAGTCTGGCTCTGTCGCCCAGGCTGGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1408451018 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7900238 48778 RMVar_ID_48778 Human_SNP_ID_415725915 A-to-I Human chr9 + 127795144 127795144 127795144 AAAATTAGCCGGGCGTGATGGTGGGCACCTGTAGTCCCAGTTAATTGGGAGGCTGAGGCAGGAGA AAAATTAGCCGGGCGTGATGGTGGGCACCTGTGGTCCCAGTTAATTGGGAGGCTGAGGCAGGAGA A G FPGS Ensembl:ENSG00000136877 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs528569478 Functional Loss SNV dbSNP153 33..33 33 - - - 48779 RMVar_ID_48779 Human_SNP_ID_415725926 A-to-I Human chr9 + 127795197 127795197 127795197 TGAGGCAGGAGAATCACTTGAACCCGGGAGGCAGAGGTTGCGGTGAGCCGGTATCACACCACTGC TGAGGCAGGAGAATCACTTGAACCCGGGAGGCGGAGGTTGCGGTGAGCCGGTATCACACCACTGC A G FPGS Ensembl:ENSG00000136877 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 29129909,30559470 RNA-Seq:(High) rs1372554444 Functional Loss SNV dbSNP153 33..33 33 - - - 48780 RMVar_ID_48780 Human_SNP_ID_415725940 A-to-I Human chr9 + 127795222 127795222 127795222 GGGAGGCAGAGGTTGCGGTGAGCCGGTATCACACCACTGCACTCCAGCCTGGGCAACAGAGCGAG GGGAGGCAGAGGTTGCGGTGAGCCGGTATCACGCCACTGCACTCCAGCCTGGGCAACAGAGCGAG A G FPGS Ensembl:ENSG00000136877 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1340843813 Functional Loss SNV dbSNP153 33..33 33 - - - 48781 RMVar_ID_48781 Human_SNP_ID_415726035 A-to-I Human chr9 + 127795376 127795376 127795376 AGAATCTCTTGAACCCGGGATGTGGAGGTTGCAGTGAGCCGAGATCAGGTCCCTGAACTCCAGCC AGAATCTCTTGAACCCGGGATGTGGAGGTTGCCGTGAGCCGAGATCAGGTCCCTGAACTCCAGCC A C FPGS Ensembl:ENSG00000136877 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1356563995 Functional Loss SNV dbSNP153 33..33 33 - - - 48782 RMVar_ID_48782 Human_SNP_ID_415726082 A-to-I Human chr9 + 127795475 127795475 127795475 ACAAAAAAAAAAAGTCGGGCACGGTGGCTCACACTTGTAATCCCAGCACTTTGGGAGGCCAAGGT ACAAAAAAAAAAAGTCGGGCACGGTGGCTCACGCTTGTAATCCCAGCACTTTGGGAGGCCAAGGT A G FPGS Ensembl:ENSG00000136877 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs960718649 Functional Loss SNV dbSNP153 33..33 33 - - - 48783 RMVar_ID_48783 Human_SNP_ID_415726083 A-to-I Human chr9 + 127795475 127795475 127795475 ACAAAAAAAAAAAGTCGGGCACGGTGGCTCACACTTGTAATCCCAGCACTTTGGGAGGCCAAGGT ACAAAAAAAAAAAGTCGGGCACGGTGGCTCACTCTTGTAATCCCAGCACTTTGGGAGGCCAAGGT A T FPGS Ensembl:ENSG00000136877 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs960718649 Functional Loss SNV dbSNP153 33..33 33 - - - 48784 RMVar_ID_48784 Human_SNP_ID_415726177 A-to-I Human chr9 + 127795690 127795690 127795690 CCGGGAGGCGGAGCTTGCAGTGAGCTGAGATCACGCCACTGCACCCCAGCCTGGGCTACAGAGCA CCGGGAGGCGGAGCTTGCAGTGAGCTGAGATCCCGCCACTGCACCCCAGCCTGGGCTACAGAGCA A C FPGS Ensembl:ENSG00000136877 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs927012101 Functional Loss SNV dbSNP153 33..33 33 - - - 48785 RMVar_ID_48785 Human_SNP_ID_415726178 A-to-I Human chr9 + 127795690 127795690 127795690 CCGGGAGGCGGAGCTTGCAGTGAGCTGAGATCACGCCACTGCACCCCAGCCTGGGCTACAGAGCA CCGGGAGGCGGAGCTTGCAGTGAGCTGAGATCGCGCCACTGCACCCCAGCCTGGGCTACAGAGCA A G FPGS Ensembl:ENSG00000136877 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs927012101 Functional Loss SNV dbSNP153 33..33 33 - - - 48786 RMVar_ID_48786 Human_SNP_ID_415726352 A-to-I Human chr9 + 127796114 127796114 127796114 ATAAATGTTTATTTGTTTTGAGACAGCGTCTTACTCTGTCACTCTGTTGCCCAGGCTGTAGCGCA ATAAATGTTTATTTGTTTTGAGACAGCGTCTTCCTCTGTCACTCTGTTGCCCAGGCTGTAGCGCA A C FPGS Ensembl:ENSG00000136877 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs540180803 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7900251 48787 RMVar_ID_48787 Human_SNP_ID_415727378 A-to-I Human chr9 + 127800083 127800083 127800083 GAACTCTAGGCTTCAAGCAATCTTCCCGCCTCAGTCTTCCAAAGTGCTAGGATTACAGGTGTGAG GAACTCTAGGCTTCAAGCAATCTTCCCGCCTCTGTCTTCCAAAGTGCTAGGATTACAGGTGTGAG A T FPGS Ensembl:ENSG00000136877 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs996375676 Functional Loss SNV dbSNP153 33..33 33 - - - 48788 RMVar_ID_48788 Human_SNP_ID_415728875 A-to-I Human chr9 + 127805324 127805324 127805324 CCAGCACTTTGGGCAGCTGACATGGGAGGATCACCTGAGTCTGGGGAGGTCAAGGCTGCAGTTAG CCAGCACTTTGGGCAGCTGACATGGGAGGATCTCCTGAGTCTGGGGAGGTCAAGGCTGCAGTTAG A T FPGS Ensembl:ENSG00000136877 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1426833741 Functional Loss SNV dbSNP153 33..33 33 - - - 48789 RMVar_ID_48789 Human_SNP_ID_415728887 A-to-I Human chr9 + 127805365 127805365 127805365 TGGGGAGGTCAAGGCTGCAGTTAGCAGTGATCATGCCATTGCACATCAGCCTGGGCGACAGAGCA TGGGGAGGTCAAGGCTGCAGTTAGCAGTGATCGTGCCATTGCACATCAGCCTGGGCGACAGAGCA A G FPGS Ensembl:ENSG00000136877 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256524431 Functional Loss SNV dbSNP153 33..33 33 - - - 48790 RMVar_ID_48790 Human_SNP_ID_415730745 A-to-I Human chr9 + 127811361 127811361 127811361 AAAATTAGCCAGGCGTAGTGGTGGGTGCCTGTAGTCTCAGCTACTCAGGAGGCTGAGGCAGGAGA AAAATTAGCCAGGCGTAGTGGTGGGTGCCTGTGGTCTCAGCTACTCAGGAGGCTGAGGCAGGAGA A G FPGS Ensembl:ENSG00000136877 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1395506469 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266214 48791 RMVar_ID_48791 Human_SNP_ID_415730968 A-to-I Human chr9 + 127812169 127812169 127812169 TACTCAGGAGGCTGAAGTGGAAGGATCGCTTGAGCCTGGAAGGTGGAGGCTGCAGTGAGTCATGA TACTCAGGAGGCTGAAGTGGAAGGATCGCTTGGGCCTGGAAGGTGGAGGCTGCAGTGAGTCATGA A G FPGS Ensembl:ENSG00000136877 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs768602787 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_266214 48792 RMVar_ID_48792 Human_SNP_ID_415733950 A-to-I Human chr9 - 127821392 127821392 127821392 AGGTCTCGCTCTGTCACCAAGGCTGGAGTGCAATGATGTGATCTCGGCTCACTGCAGCCTCCTCC AGGTCTCGCTCTGTCACCAAGGCTGGAGTGCAGTGATGTGATCTCGGCTCACTGCAGCCTCCTCC T C ENG Ensembl:ENSG00000106991 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1040388071 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82199,RMVar_hsa_circ_259811,RMVar_hsa_circ_92630,RMVar_hsa_circ_259812 48793 RMVar_ID_48793 Human_SNP_ID_415755462 A-to-I Human chr9 - 127901372 127901372 127901372 TTAGCCAGGCTGGTCTCGAACTCCTGACCTCAAGTGATCCGCCTGCCTCCCCTCCCAAAGTGCTG TTAGCCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCCGCCTGCCTCCCCTCCCAAAGTGCTG T C ST6GALNAC6,AL157935.3 Ensembl:ENSG00000160408,Ensembl:ENSG00000257524 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917402663 Functional Loss SNV dbSNP153 33..33 33 - - - 48794 RMVar_ID_48794 Human_SNP_ID_415755486 A-to-I Human chr9 - 127901427 127901427 127901427 CCACCACGCCTGGCTAATTTATTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTAGCCAGGC CCACCACGCCTGGCTAATTTATTTGTATTTTTGGTAGAGACGGGGTTTCACCATGTTAGCCAGGC T C ST6GALNAC6,AL157935.3 Ensembl:ENSG00000160408,Ensembl:ENSG00000257524 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1402262478 Functional Loss SNV dbSNP153 33..33 33 - - - 48795 RMVar_ID_48795 Human_SNP_ID_415756903 A-to-I Human chr9 - 127906949 127906949 127906949 TGACACCAGTGTGGCCAACAGGGTGAAATCCCATCTCTACTAAAAATACAAAAAATTAGTAGGAT TGACACCAGTGTGGCCAACAGGGTGAAATCCCGTCTCTACTAAAAATACAAAAAATTAGTAGGAT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1208753116 Functional Loss SNV dbSNP153 33..33 33 - - - 48796 RMVar_ID_48796 Human_SNP_ID_415756910 A-to-I Human chr9 - 127906985 127906985 127906985 AGGCCGAGGTGGGCAGATCACTTGGGGTCAGAAGTCTGACACCAGTGTGGCCAACAGGGTGAAAT AGGCCGAGGTGGGCAGATCACTTGGGGTCAGAGGTCTGACACCAGTGTGGCCAACAGGGTGAAAT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1333078544 Functional Loss SNV dbSNP153 33..33 33 - - - 48797 RMVar_ID_48797 Human_SNP_ID_415757572 A-to-I Human chr9 - 127909225 127909225 127909225 GCCACCACGCCCAGCTAATTTTTTGTAGTTTTAGTAGAGACGGGGTTTCATCATGTTGGCCAGGC GCCACCACGCCCAGCTAATTTTTTGTAGTTTTGGTAGAGACGGGGTTTCATCATGTTGGCCAGGC T C ST6GALNAC4 Ensembl:ENSG00000136840 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1446345396 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108756,RMVar_hsa_circ_259819,RMVar_hsa_circ_91504,RMVar_hsa_circ_105777,RMVar_hsa_circ_259820,RMVar_hsa_circ_259821 48798 RMVar_ID_48798 Human_SNP_ID_415798864 A-to-I Human chr9 - 128064743 128064743 128064743 CCACCTCGGCCTCCCAAAGTGCTGGGATTACAAGCGTGAGCCACCGCGCCCGGCCGGGGGTGCCT CCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCCCGGCCGGGGGTGCCT T C NAIF1 Ensembl:ENSG00000171169 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1040837123 Functional Loss SNV dbSNP153 33..33 33 - - - 48799 RMVar_ID_48799 Human_SNP_ID_415798999 A-to-I Human chr9 - 128065255 128065255 128065255 AAAATTACCCAGGCTTGGAGGTGGGCGACTGTAGTCCCAGCTACTCGGGAGGCTGAGGCACAACA AAAATTACCCAGGCTTGGAGGTGGGCGACTGTGGTCCCAGCTACTCGGGAGGCTGAGGCACAACA T C NAIF1 Ensembl:ENSG00000171169 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1478766455 Functional Loss SNV dbSNP153 33..33 33 - - - 48800 RMVar_ID_48800 Human_SNP_ID_415810292 A-to-I Human chr9 + 128108177 128108177 128108177 TGGTGCTCTGAGCTGGCCTGGACCCTGTCAGGATGGGCCCCACCTCAGAACCAAACTCACTGTCC TGGTGCTCTGAGCTGGCCTGGACCCTGTCAGGGTGGGCCCCACCTCAGAACCAAACTCACTGTCC A G SLC25A25 Ensembl:ENSG00000148339 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs770879666 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7900368,Human_RBP_ID_26565297,Human_RBP_ID_27542371 48801 RMVar_ID_48801 Human_SNP_ID_415811417 A-to-I Human chr9 - 128112389 128112389 128112389 CAGGCTGGAGTTCAGTGGCGCGATCTTGGCTCACTGCAACCTCTGTCTTCCAGGTTCAAGCAATT CAGGCTGGAGTTCAGTGGCGCGATCTTGGCTCCCTGCAACCTCTGTCTTCCAGGTTCAAGCAATT T G SLC25A25-AS1 Ensembl:ENSG00000234771 lincRNA exon GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1002410434 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107826,RMVar_hsa_circ_259837 48802 RMVar_ID_48802 Human_SNP_ID_415811585 A-to-I Human chr9 - 128113045 128113045 128113045 ACCTCAGGTGATCCACCTGCATCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGTGC ACCTCAGGTGATCCACCTGCATCGGCCTCCCACAGTGCTGGGATTACAGGCATGAGCCACCGTGC T G SLC25A25-AS1 Ensembl:ENSG00000234771 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1330163885 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107826,RMVar_hsa_circ_259837 48803 RMVar_ID_48803 Human_SNP_ID_415811610 A-to-I Human chr9 - 128113127 128113126 128113127 ACGCCCAGCTCATTTTTTTTTTTTTTTTTTTTAGTAGAGACGGGGTTTACACCATGTTGGCCAGG ACGCCCAGCTCATTTTTTTTTTTTTTTTTTTT_GTAGAGACGGGGTTTACACCATGTTGGCCAGG CT C SLC25A25-AS1 Ensembl:ENSG00000234771 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1440107361 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_107826,RMVar_hsa_circ_259837 48804 RMVar_ID_48804 Human_SNP_ID_415811611 A-to-I Human chr9 - 128113127 128113127 128113127 ACGCCCAGCTCATTTTTTTTTTTTTTTTTTTTAGTAGAGACGGGGTTTACACCATGTTGGCCAGG ACGCCCAGCTCATTTTTTTTTTTTTTTTTTTTTGTAGAGACGGGGTTTACACCATGTTGGCCAGG T A SLC25A25-AS1 Ensembl:ENSG00000234771 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1248822880 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107826,RMVar_hsa_circ_259837 48805 RMVar_ID_48805 Human_SNP_ID_415829016 A-to-I Human chr9 - 128165061 128165061 128165061 TTTAGTATAGACAGGGTTTCGCCATGTTGGCGAGGCTGGTCTTGAACTCCTGACCTTAAATGATC TTTAGTATAGACAGGGTTTCGCCATGTTGGCGGGGCTGGTCTTGAACTCCTGACCTTAAATGATC T C CIZ1 Ensembl:ENSG00000148337 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1408364927 Functional Loss SNV dbSNP153 33..33 33 - - - 48806 RMVar_ID_48806 Human_SNP_ID_415829021 A-to-I Human chr9 - 128165081 128165079 128165081 CACGCCCAACTTTTTGTATTTTTAGTATAGACAGGGTTTCGCCATGTTGGCGAGGCTGGTCTTGA CACGCCCAACTTTTTGTATTTTTAGTATAGAC__GGTTTCGCCATGTTGGCGAGGCTGGTCTTGA CCT C CIZ1 Ensembl:ENSG00000148337 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417073632 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_22837727 48807 RMVar_ID_48807 Human_SNP_ID_415829022 A-to-I Human chr9 - 128165081 128165081 128165081 CACGCCCAACTTTTTGTATTTTTAGTATAGACAGGGTTTCGCCATGTTGGCGAGGCTGGTCTTGA CACGCCCAACTTTTTGTATTTTTAGTATAGACTGGGTTTCGCCATGTTGGCGAGGCTGGTCTTGA T A CIZ1 Ensembl:ENSG00000148337 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs771225259 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22837727 48808 RMVar_ID_48808 Human_SNP_ID_415834319 A-to-I Human chr9 - 128183961 128183961 128183961 GAGTCCAAGACCAGCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCT GAGTCCAAGACCAGCCTGGCCAACATGGTGAATCCCCGTCTCTACTAAAAATACAAAAATTAGCT T A CIZ1 Ensembl:ENSG00000148337 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs771031064 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124004,RMVar_hsa_circ_259851,RMVar_hsa_circ_98321,RMVar_hsa_circ_259853,RMVar_hsa_circ_371308,RMVar_hsa_circ_259855,RMVar_hsa_circ_121499,RMVar_hsa_circ_53018,RMVar_hsa_circ_259856 48809 RMVar_ID_48809 Human_SNP_ID_415836616 A-to-I Human chr9 - 128192635 128192635 128192635 TGGAAGCTGAGGCGGGAGGACCACTTGAACCCAGGAGGCGGAGGTTGCGGTGAGCCCAGATCGTG TGGAAGCTGAGGCGGGAGGACCACTTGAACCCTGGAGGCGGAGGTTGCGGTGAGCCCAGATCGTG T A CIZ1 Ensembl:ENSG00000148337 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1026468780 Functional Loss SNV dbSNP153 33..33 33 - - - 48810 RMVar_ID_48810 Human_SNP_ID_415836636 A-to-I Human chr9 - 128192722 128192722 128192722 CCTGACCAACATGGTGAAGCCCCGTCTCTATTAAAAATACAAAAATTAGCCGGGCGTGGTGGCCC CCTGACCAACATGGTGAAGCCCCGTCTCTATTGAAAATACAAAAATTAGCCGGGCGTGGTGGCCC T C CIZ1 Ensembl:ENSG00000148337 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1030744003 Functional Loss SNV dbSNP153 33..33 33 - - - 48811 RMVar_ID_48811 Human_SNP_ID_415838398 A-to-I Human chr9 + 128199892 128199892 128199892 GCAACCACCACCCCTGCCTCCCAGGTTCAAGCAATTCTCCCACCTCAGCCTCTCGAGTACCTGGG GCAACCACCACCCCTGCCTCCCAGGTTCAAGCTATTCTCCCACCTCAGCCTCTCGAGTACCTGGG A T DNM1 Ensembl:ENSG00000106976 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348098510 Functional Loss SNV dbSNP153 33..33 33 - - - 48812 RMVar_ID_48812 Human_SNP_ID_415838401 A-to-I Human chr9 + 128199901 128199901 128199901 ACCCCTGCCTCCCAGGTTCAAGCAATTCTCCCACCTCAGCCTCTCGAGTACCTGGGATTACAGGT ACCCCTGCCTCCCAGGTTCAAGCAATTCTCCCCCCTCAGCCTCTCGAGTACCTGGGATTACAGGT A C DNM1 Ensembl:ENSG00000106976 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1165309230 Functional Loss SNV dbSNP153 33..33 33 - - - 48813 RMVar_ID_48813 Human_SNP_ID_415845780 A-to-I Human chr9 + 128227888 128227888 128227888 TTCTTTCTTTTTTAGAGACGGGGTTTTGCTGTATCTCCCAGCATGGAGTGCAGTGGCACAATCAT TTCTTTCTTTTTTAGAGACGGGGTTTTGCTGTGTCTCCCAGCATGGAGTGCAGTGGCACAATCAT A G DNM1 Ensembl:ENSG00000106976 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1255949950 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_712449,Human_RBP_ID_16583018,Human_RBP_ID_17579116 RMVar_hsa_circ_102982,RMVar_hsa_circ_259861,RMVar_hsa_circ_119887,RMVar_hsa_circ_37787,RMVar_hsa_circ_259864,RMVar_hsa_circ_266039,RMVar_hsa_circ_84213,RMVar_hsa_circ_259865,RMVar_hsa_circ_37426,RMVar_hsa_circ_126553,RMVar_hsa_circ_259866,RMVar_hsa_circ_259867 48814 RMVar_ID_48814 Human_SNP_ID_415845817 A-to-I Human chr9 + 128228064 128228063 128228065 TTTGTTTGTTTGTTTTTGGTTTTTTTTGAGACAGAGTTTCACGCTTGTTGCCCAGGCTGGAGTGC TTTGTTTGTTTGTTTTTGGTTTTTTTTGAGAC__AGTTTCACGCTTGTTGCCCAGGCTGGAGTGC CAG C DNM1 Ensembl:ENSG00000106976 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1367441808 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_102982,RMVar_hsa_circ_259861,RMVar_hsa_circ_119887,RMVar_hsa_circ_37787,RMVar_hsa_circ_259864,RMVar_hsa_circ_266039,RMVar_hsa_circ_84213,RMVar_hsa_circ_259865,RMVar_hsa_circ_37426,RMVar_hsa_circ_126553,RMVar_hsa_circ_259866,RMVar_hsa_circ_259867 48815 RMVar_ID_48815 Human_SNP_ID_415845826 A-to-I Human chr9 + 128228106 128228106 128228106 GCTTGTTGCCCAGGCTGGAGTGCAGTGGTGCCATCTCGGCTCACTGCAACCTCCACCTCTCAGGT GCTTGTTGCCCAGGCTGGAGTGCAGTGGTGCCTTCTCGGCTCACTGCAACCTCCACCTCTCAGGT A T DNM1 Ensembl:ENSG00000106976 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1166678300 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102982,RMVar_hsa_circ_259861,RMVar_hsa_circ_119887,RMVar_hsa_circ_37787,RMVar_hsa_circ_259864,RMVar_hsa_circ_266039,RMVar_hsa_circ_84213,RMVar_hsa_circ_259865,RMVar_hsa_circ_37426,RMVar_hsa_circ_126553,RMVar_hsa_circ_259866,RMVar_hsa_circ_259867 48816 RMVar_ID_48816 Human_SNP_ID_415845834 A-to-I Human chr9 + 128228128 128228128 128228128 CAGTGGTGCCATCTCGGCTCACTGCAACCTCCACCTCTCAGGTTCAAGCGATTCTCCTGCCTCAG CAGTGGTGCCATCTCGGCTCACTGCAACCTCCTCCTCTCAGGTTCAAGCGATTCTCCTGCCTCAG A T DNM1 Ensembl:ENSG00000106976 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1451977338 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102982,RMVar_hsa_circ_259861,RMVar_hsa_circ_119887,RMVar_hsa_circ_37787,RMVar_hsa_circ_259864,RMVar_hsa_circ_266039,RMVar_hsa_circ_84213,RMVar_hsa_circ_259865,RMVar_hsa_circ_37426,RMVar_hsa_circ_126553,RMVar_hsa_circ_259866,RMVar_hsa_circ_259867 48817 RMVar_ID_48817 Human_SNP_ID_415845868 A-to-I Human chr9 + 128228323 128228323 128228323 CCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCCCTCCTGGCCTAATAATTTTTTT CCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCCCTCCTGGCCTAATAATTTTTTT A G DNM1 Ensembl:ENSG00000106976 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1280920732 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102982,RMVar_hsa_circ_259861,RMVar_hsa_circ_119887,RMVar_hsa_circ_37787,RMVar_hsa_circ_259864,RMVar_hsa_circ_266039,RMVar_hsa_circ_84213,RMVar_hsa_circ_259865,RMVar_hsa_circ_37426,RMVar_hsa_circ_126553,RMVar_hsa_circ_259866,RMVar_hsa_circ_259867 48818 RMVar_ID_48818 Human_SNP_ID_415845877 A-to-I Human chr9 + 128228359 128228359 128228359 GCCACCCCTCCTGGCCTAATAATTTTTTTGTTAAGACAGGATCTTACTATGTTGCCCAGGCTGCT GCCACCCCTCCTGGCCTAATAATTTTTTTGTTCAGACAGGATCTTACTATGTTGCCCAGGCTGCT A C DNM1 Ensembl:ENSG00000106976 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs868015551 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102982,RMVar_hsa_circ_259861,RMVar_hsa_circ_119887,RMVar_hsa_circ_37787,RMVar_hsa_circ_259864,RMVar_hsa_circ_266039,RMVar_hsa_circ_84213,RMVar_hsa_circ_259865,RMVar_hsa_circ_37426,RMVar_hsa_circ_126553,RMVar_hsa_circ_259866,RMVar_hsa_circ_259867 48819 RMVar_ID_48819 Human_SNP_ID_415845889 A-to-I Human chr9 + 128228455 128228455 128228455 CTTCAGCCTCCCAAAATGCTGGGTTTATAGGCATGAGCCACCATCTGGCAACAGTGGCTTCTTGA CTTCAGCCTCCCAAAATGCTGGGTTTATAGGCGTGAGCCACCATCTGGCAACAGTGGCTTCTTGA A G DNM1 Ensembl:ENSG00000106976 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1189405099 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17579117 RMVar_hsa_circ_102982,RMVar_hsa_circ_259861,RMVar_hsa_circ_119887,RMVar_hsa_circ_37787,RMVar_hsa_circ_259864,RMVar_hsa_circ_266039,RMVar_hsa_circ_84213,RMVar_hsa_circ_259865,RMVar_hsa_circ_37426,RMVar_hsa_circ_126553,RMVar_hsa_circ_259866,RMVar_hsa_circ_259867 48820 RMVar_ID_48820 Human_SNP_ID_415846119 A-to-I Human chr9 + 128229432 128229432 128229432 CAGCCTGGGCAACATAGTAAGACCCTGTCTCTACAAAAAATAAAAAGATTAGCTGGGCATGATGG CAGCCTGGGCAACATAGTAAGACCCTGTCTCTGCAAAAAATAAAAAGATTAGCTGGGCATGATGG A G DNM1 Ensembl:ENSG00000106976 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs553167760 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102982,RMVar_hsa_circ_259861,RMVar_hsa_circ_119887,RMVar_hsa_circ_37787,RMVar_hsa_circ_259864,RMVar_hsa_circ_266039,RMVar_hsa_circ_84213,RMVar_hsa_circ_259865,RMVar_hsa_circ_37426,RMVar_hsa_circ_126553,RMVar_hsa_circ_259866,RMVar_hsa_circ_259867 48821 RMVar_ID_48821 Human_SNP_ID_415846128 A-to-I Human chr9 + 128229458 128229458 128229458 GTCTCTACAAAAAATAAAAAGATTAGCTGGGCATGATGGCACACGCCTGTAGTCCCAGCTACTTA GTCTCTACAAAAAATAAAAAGATTAGCTGGGCGTGATGGCACACGCCTGTAGTCCCAGCTACTTA A G DNM1 Ensembl:ENSG00000106976 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1462247789 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102982,RMVar_hsa_circ_259861,RMVar_hsa_circ_119887,RMVar_hsa_circ_37787,RMVar_hsa_circ_259864,RMVar_hsa_circ_266039,RMVar_hsa_circ_84213,RMVar_hsa_circ_259865,RMVar_hsa_circ_37426,RMVar_hsa_circ_126553,RMVar_hsa_circ_259866,RMVar_hsa_circ_259867 48822 RMVar_ID_48822 Human_SNP_ID_415846538 A-to-I Human chr9 + 128230932 128230932 128230932 TCAAACGATTCTTATGCCTCAGCCTCCTGAGTAGCTGTGATTAAAGGCATGTGCCACCACACCCA TCAAACGATTCTTATGCCTCAGCCTCCTGAGTGGCTGTGATTAAAGGCATGTGCCACCACACCCA A G DNM1 Ensembl:ENSG00000106976 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1271941142 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102982,RMVar_hsa_circ_259861,RMVar_hsa_circ_119887,RMVar_hsa_circ_37787,RMVar_hsa_circ_259864,RMVar_hsa_circ_266039,RMVar_hsa_circ_84213,RMVar_hsa_circ_259865,RMVar_hsa_circ_37426,RMVar_hsa_circ_126553,RMVar_hsa_circ_259866,RMVar_hsa_circ_259867 48823 RMVar_ID_48823 Human_SNP_ID_415846553 A-to-I Human chr9 + 128231003 128231003 128231003 TTTTGTATTTTTGGTAGAGATGGGATTTCACCATGTTAGCCAGGCTGGTCTCAAACTCCTGACCT TTTTGTATTTTTGGTAGAGATGGGATTTCACCGTGTTAGCCAGGCTGGTCTCAAACTCCTGACCT A G DNM1 Ensembl:ENSG00000106976 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1300672190 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102982,RMVar_hsa_circ_259861,RMVar_hsa_circ_119887,RMVar_hsa_circ_37787,RMVar_hsa_circ_259864,RMVar_hsa_circ_266039,RMVar_hsa_circ_84213,RMVar_hsa_circ_259865,RMVar_hsa_circ_37426,RMVar_hsa_circ_126553,RMVar_hsa_circ_259866,RMVar_hsa_circ_259867 48824 RMVar_ID_48824 Human_SNP_ID_415846659 A-to-I Human chr9 + 128231302 128231302 128231302 TCAGCTTACTGCAACCTCCACCTCCTGGGTCCAAGTGATTCTCCTGCCTCAGCCTCCGAGTAGCT TCAGCTTACTGCAACCTCCACCTCCTGGGTCCGAGTGATTCTCCTGCCTCAGCCTCCGAGTAGCT A G DNM1 Ensembl:ENSG00000106976 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs931610322 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102982,RMVar_hsa_circ_259861,RMVar_hsa_circ_119887,RMVar_hsa_circ_37787,RMVar_hsa_circ_259864,RMVar_hsa_circ_266039,RMVar_hsa_circ_84213,RMVar_hsa_circ_259865,RMVar_hsa_circ_37426,RMVar_hsa_circ_126553,RMVar_hsa_circ_259866,RMVar_hsa_circ_259867 48825 RMVar_ID_48825 Human_SNP_ID_415846660 A-to-I Human chr9 + 128231302 128231302 128231302 TCAGCTTACTGCAACCTCCACCTCCTGGGTCCAAGTGATTCTCCTGCCTCAGCCTCCGAGTAGCT TCAGCTTACTGCAACCTCCACCTCCTGGGTCCTAGTGATTCTCCTGCCTCAGCCTCCGAGTAGCT A T DNM1 Ensembl:ENSG00000106976 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs931610322 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102982,RMVar_hsa_circ_259861,RMVar_hsa_circ_119887,RMVar_hsa_circ_37787,RMVar_hsa_circ_259864,RMVar_hsa_circ_266039,RMVar_hsa_circ_84213,RMVar_hsa_circ_259865,RMVar_hsa_circ_37426,RMVar_hsa_circ_126553,RMVar_hsa_circ_259866,RMVar_hsa_circ_259867 48826 RMVar_ID_48826 Human_SNP_ID_415846671 A-to-I Human chr9 + 128231341 128231341 128231341 TCTCCTGCCTCAGCCTCCGAGTAGCTGGGATTACAGGCATGTGCCACCACGCCCGGCTACTTTTG TCTCCTGCCTCAGCCTCCGAGTAGCTGGGATTTCAGGCATGTGCCACCACGCCCGGCTACTTTTG A T DNM1 Ensembl:ENSG00000106976 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs539866432 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102982,RMVar_hsa_circ_259861,RMVar_hsa_circ_119887,RMVar_hsa_circ_37787,RMVar_hsa_circ_259864,RMVar_hsa_circ_266039,RMVar_hsa_circ_84213,RMVar_hsa_circ_259865,RMVar_hsa_circ_37426,RMVar_hsa_circ_126553,RMVar_hsa_circ_259866,RMVar_hsa_circ_259867 48827 RMVar_ID_48827 Human_SNP_ID_415855437 A-to-I Human chr9 - 128263613 128263613 128263613 GAGATCGAGACCATCCTTGCTAACACAGTGAAACCTCGTCTCTACTAAAAATACAAAAAAATTAG GAGATCGAGACCATCCTTGCTAACACAGTGAAGCCTCGTCTCTACTAAAAATACAAAAAAATTAG T C GOLGA2 Ensembl:ENSG00000167110 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1280187765 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24354,RMVar_hsa_circ_88892,RMVar_hsa_circ_259870,RMVar_hsa_circ_78346,RMVar_hsa_circ_259879,RMVar_hsa_circ_93901,RMVar_hsa_circ_78529,RMVar_hsa_circ_88631,RMVar_hsa_circ_259880,RMVar_hsa_circ_126268,RMVar_hsa_circ_259881,RMVar_hsa_circ_123616,RMVar_hsa_circ_259882,RMVar_hsa_circ_259884,RMVar_hsa_circ_259883,RMVar_hsa_circ_259886,RMVar_hsa_circ_109658 48828 RMVar_ID_48828 Human_SNP_ID_415855440 A-to-I Human chr9 - 128263619 128263619 128263619 GGTCAGGAGATCGAGACCATCCTTGCTAACACAGTGAAACCTCGTCTCTACTAAAAATACAAAAA GGTCAGGAGATCGAGACCATCCTTGCTAACACCGTGAAACCTCGTCTCTACTAAAAATACAAAAA T G GOLGA2 Ensembl:ENSG00000167110 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1005545025 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24354,RMVar_hsa_circ_88892,RMVar_hsa_circ_259870,RMVar_hsa_circ_78346,RMVar_hsa_circ_259879,RMVar_hsa_circ_93901,RMVar_hsa_circ_78529,RMVar_hsa_circ_88631,RMVar_hsa_circ_259880,RMVar_hsa_circ_126268,RMVar_hsa_circ_259881,RMVar_hsa_circ_123616,RMVar_hsa_circ_259882,RMVar_hsa_circ_259884,RMVar_hsa_circ_259883,RMVar_hsa_circ_259886,RMVar_hsa_circ_109658 48829 RMVar_ID_48829 Human_SNP_ID_415857216 A-to-I Human chr9 - 128270226 128270226 128270226 TTGGGAGGCTGAAGCAGGAGAATCTCGAACTCAGGAGGCGGAGGTTGCAGTGAGTGGAGATCTCG TTGGGAGGCTGAAGCAGGAGAATCTCGAACTCTGGAGGCGGAGGTTGCAGTGAGTGGAGATCTCG T A GOLGA2 Ensembl:ENSG00000167110 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1265115078 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74727,RMVar_hsa_circ_126268,RMVar_hsa_circ_259882,RMVar_hsa_circ_120738,RMVar_hsa_circ_259890 48830 RMVar_ID_48830 Human_SNP_ID_415859170 A-to-I Human chr9 + 128277290 128277290 128277290 GTAGATCGTGAGGGCCGGGTGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGC GTAGATCGTGAGGGCCGGGTGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGC A G SWI5 Ensembl:ENSG00000175854 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1030097770 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77572,RMVar_hsa_circ_259891,RMVar_hsa_circ_77558,RMVar_hsa_circ_101837,RMVar_hsa_circ_259892,RMVar_hsa_circ_259893 48831 RMVar_ID_48831 Human_SNP_ID_415861777 A-to-I Human chr9 + 128287291 128287290 128287291 ACGCAGTGAAACCCTGTCTCTACTGAAAATACAAAAATTAGCTAGGTGTGGTGGCACATGCCTGT ACGCAGTGAAACCCTGTCTCTACTGAAAATAC_AAAATTAGCTAGGTGTGGTGGCACATGCCTGT CA C SWI5 Ensembl:ENSG00000175854 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1564375964 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_259891,RMVar_hsa_circ_77558,RMVar_hsa_circ_101837,RMVar_hsa_circ_126252,RMVar_hsa_circ_259893,RMVar_hsa_circ_83200,RMVar_hsa_circ_259894,RMVar_hsa_circ_259895 48832 RMVar_ID_48832 Human_SNP_ID_415861932 A-to-I Human chr9 + 128287831 128287831 128287831 TGATCCACCCACCTTGGCCTCCCAAAGTGCTGAGATTATAGGCTGAGCCACCGCACCTGGCATCC TGATCCACCCACCTTGGCCTCCCAAAGTGCTGGGATTATAGGCTGAGCCACCGCACCTGGCATCC A G SWI5 Ensembl:ENSG00000175854 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1371461858 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_259891,RMVar_hsa_circ_77558,RMVar_hsa_circ_101837,RMVar_hsa_circ_126252,RMVar_hsa_circ_259893,RMVar_hsa_circ_83200,RMVar_hsa_circ_259894,RMVar_hsa_circ_259895 48833 RMVar_ID_48833 Human_SNP_ID_415866481 A-to-I Human chr9 - 128305402 128305402 128305402 GTACTCTAGCCTGGGTGACAGGGTGAGACCCTATCTCAAAACAAACAAACAAAAACCCCACCAGC GTACTCTAGCCTGGGTGACAGGGTGAGACCCTGTCTCAAAACAAACAAACAAAAACCCCACCAGC T C TRUB2 Ensembl:ENSG00000167112 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs11557596 Functional Loss SNV dbSNP153 33..33 33 - - - 48834 RMVar_ID_48834 Human_SNP_ID_415866514 A-to-I Human chr9 - 128305545 128305545 128305545 GTCTCTACCAAAAATACAAAAATTAGCCGGGCATGGTGGCGCTTGTCTGTAGTCCAGCTACAGCT GTCTCTACCAAAAATACAAAAATTAGCCGGGCCTGGTGGCGCTTGTCTGTAGTCCAGCTACAGCT T G TRUB2 Ensembl:ENSG00000167112 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs752941816 Functional Loss SNV dbSNP153 33..33 33 - - - 48835 RMVar_ID_48835 Human_SNP_ID_415866563 A-to-I Human chr9 - 128305734 128305734 128305734 AGTAAATGGAGATCTGTACTCCAGCCTGGGCAACAGAGCGAGACCCTATGTCAGAAAAAAAGAAA AGTAAATGGAGATCTGTACTCCAGCCTGGGCAGCAGAGCGAGACCCTATGTCAGAAAAAAAGAAA T C TRUB2 Ensembl:ENSG00000167112 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1008066508 Functional Loss SNV dbSNP153 33..33 33 - - - 48836 RMVar_ID_48836 Human_SNP_ID_415866583 A-to-I Human chr9 - 128305822 128305822 128305822 AGCCGGGGGTGTTGGTGTGTGCCTGTAGTCCCAGCTACTAGGGAGGCTGAGATGGGAGGATCGCT AGCCGGGGGTGTTGGTGTGTGCCTGTAGTCCCGGCTACTAGGGAGGCTGAGATGGGAGGATCGCT T C TRUB2 Ensembl:ENSG00000167112 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1304946982 Functional Loss SNV dbSNP153 33..33 33 - - - 48837 RMVar_ID_48837 Human_SNP_ID_415866788 A-to-I Human chr9 - 128306568 128306556 128306568 GGGCGTGCTTGCACGTGCCTGTAGTCCTGGCTACCCGGGAGGCTGATGCAGAATAACTGGAACTC GGGCGTGCTTGCACGTGCCTGTAGTCCTGGCT____________GATGCAGAATAACTGGAACTC CAGCCTCCCGGGT C TRUB2 Ensembl:ENSG00000167112 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1212653823 Functional Loss DEL dbSNP153 33..44 33 - - - Human_RBP_ID_16583375 48838 RMVar_ID_48838 Human_SNP_ID_415866809 A-to-I Human chr9 - 128306631 128306631 128306631 GAGTTCAAGACCAGCCTGACCAACATGGTGAAACCTGTCTCTACTAAAAATACAAAATTAGCCGG GAGTTCAAGACCAGCCTGACCAACATGGTGAAGCCTGTCTCTACTAAAAATACAAAATTAGCCGG T C TRUB2 Ensembl:ENSG00000167112 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1308824619 Functional Loss SNV dbSNP153 33..33 33 - - - 48839 RMVar_ID_48839 Human_SNP_ID_415866819 A-to-I Human chr9 - 128306665 128306665 128306665 TTGGGAGGCCAGGGTGGGCGGATCACGAGGTCAGGAGTTCAAGACCAGCCTGACCAACATGGTGA TTGGGAGGCCAGGGTGGGCGGATCACGAGGTCCGGAGTTCAAGACCAGCCTGACCAACATGGTGA T G TRUB2 Ensembl:ENSG00000167112 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs950489930 Functional Loss SNV dbSNP153 33..33 33 - - - 48840 RMVar_ID_48840 Human_SNP_ID_415866856 A-to-I Human chr9 - 128306783 128306783 128306783 TGCCATTAGCTGAGATTGTGCCCCTGCACTCCAGTCTGGACGAGAGAGTGAGACTCTGTCTCAGA TGCCATTAGCTGAGATTGTGCCCCTGCACTCCCGTCTGGACGAGAGAGTGAGACTCTGTCTCAGA T G TRUB2 Ensembl:ENSG00000167112 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1182587710 Functional Loss SNV dbSNP153 33..33 33 - - - 48841 RMVar_ID_48841 Human_SNP_ID_415866872 A-to-I Human chr9 - 128306845 128306845 128306845 TGTAATCCTAGCTACTTGGGAGGCTGAGGCACAAGAATCGCTGAAGCCCAGGAGGTGGAGATTGC TGTAATCCTAGCTACTTGGGAGGCTGAGGCACGAGAATCGCTGAAGCCCAGGAGGTGGAGATTGC T C TRUB2 Ensembl:ENSG00000167112 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335302988 Functional Loss SNV dbSNP153 33..33 33 - - - 48842 RMVar_ID_48842 Human_SNP_ID_415866887 A-to-I Human chr9 - 128306900 128306900 128306900 GAAACCCTGTCTCTACTAAAAATACAAAAATTAGCCAGCTATGGTGACGCACTTCTGTAATCCTA GAAACCCTGTCTCTACTAAAAATACAAAAATTCGCCAGCTATGGTGACGCACTTCTGTAATCCTA T G TRUB2 Ensembl:ENSG00000167112 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1188042678 Functional Loss SNV dbSNP153 33..33 33 - - - 48843 RMVar_ID_48843 Human_SNP_ID_415866936 A-to-I Human chr9 - 128307094 128307094 128307094 CACCACCACGCCCAGCTAACTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGACATGC CACCACCACGCCCAGCTAACTTTTGTATTTTTGGTAGAGACGGGGTTTCACCATGTTGGACATGC T C TRUB2 Ensembl:ENSG00000167112 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs912685932 Functional Loss SNV dbSNP153 33..33 33 - - - 48844 RMVar_ID_48844 Human_SNP_ID_415866990 A-to-I Human chr9 - 128307319 128307319 128307319 TTCCCACCTCACCCTCCAGAATAGCTGGGACTACAGGCGTGCACCACGATGCCTGGCTAAATATT TTCCCACCTCACCCTCCAGAATAGCTGGGACTGCAGGCGTGCACCACGATGCCTGGCTAAATATT T C TRUB2 Ensembl:ENSG00000167112 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1233591739 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16583377 48845 RMVar_ID_48845 Human_SNP_ID_415867130 A-to-I Human chr9 - 128307726 128307724 128307726 CTAATTTATTTATTTTATTTTATTTTTGAGACAGGGCCTCGCACTGTCGCCCAGGCTAGAGTGCA CTAATTTATTTATTTTATTTTATTTTTGAGAC__GGCCTCGCACTGTCGCCCAGGCTAGAGTGCA CCT C TRUB2 Ensembl:ENSG00000167112 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1263723658 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_16583378 48846 RMVar_ID_48846 Human_SNP_ID_415867188 A-to-I Human chr9 - 128307934 128307934 128307934 CCTCTGCCTCCCAAAGCACTGGGATGGCAGGCATGAGCCACCACACCCGGCCTGTTTTTGTTTTT CCTCTGCCTCCCAAAGCACTGGGATGGCAGGCGTGAGCCACCACACCCGGCCTGTTTTTGTTTTT T C TRUB2 Ensembl:ENSG00000167112 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1305014206 Functional Loss SNV dbSNP153 33..33 33 - - - 48847 RMVar_ID_48847 Human_SNP_ID_415867259 A-to-I Human chr9 - 128308216 128308212 128308216 TTTGGTTTTTTTTTTTTCTGAGACGGAGTCTCACTCCGTCATCCAGGTTGGAGTGCAGTGGCACA TTTGGTTTTTTTTTTTTCTGAGACGGAGTCTC____CGTCATCCAGGTTGGAGTGCAGTGGCACA GGAGT G TRUB2 Ensembl:ENSG00000167112 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1342455165 Functional Loss DEL dbSNP153 33..36 33 - - - 48848 RMVar_ID_48848 Human_SNP_ID_415867263 A-to-I Human chr9 - 128308216 128308216 128308216 TTTGGTTTTTTTTTTTTCTGAGACGGAGTCTCACTCCGTCATCCAGGTTGGAGTGCAGTGGCACA TTTGGTTTTTTTTTTTTCTGAGACGGAGTCTCGCTCCGTCATCCAGGTTGGAGTGCAGTGGCACA T C TRUB2 Ensembl:ENSG00000167112 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1354120561 Functional Loss SNV dbSNP153 33..33 33 - - - 48849 RMVar_ID_48849 Human_SNP_ID_415867264 A-to-I Human chr9 - 128308216 128308216 128308216 TTTGGTTTTTTTTTTTTCTGAGACGGAGTCTCACTCCGTCATCCAGGTTGGAGTGCAGTGGCACA TTTGGTTTTTTTTTTTTCTGAGACGGAGTCTCCCTCCGTCATCCAGGTTGGAGTGCAGTGGCACA T G TRUB2 Ensembl:ENSG00000167112 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1354120561 Functional Loss SNV dbSNP153 33..33 33 - - - 48850 RMVar_ID_48850 Human_SNP_ID_415867352 A-to-I Human chr9 - 128308483 128308483 128308483 GTGGCCCAGGCTGGAGTGCAGTGGTGCGATCTAGGCTCACTGCAACCTCCGCTTCCCAGGTTCAC GTGGCCCAGGCTGGAGTGCAGTGGTGCGATCTCGGCTCACTGCAACCTCCGCTTCCCAGGTTCAC T G TRUB2 Ensembl:ENSG00000167112 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs906730699 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16583386 48851 RMVar_ID_48851 Human_SNP_ID_415867575 A-to-I Human chr9 - 128309199 128309199 128309199 TAGACGGCGCCTGTGAATAGCCACTGCACTCTAGTCTGGGGAACATATGAGACCCCTGCCATCTC TAGACGGCGCCTGTGAATAGCCACTGCACTCTCGTCTGGGGAACATATGAGACCCCTGCCATCTC T G TRUB2 Ensembl:ENSG00000167112 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs941816178 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_712493,Human_RBP_ID_1058030,Human_RBP_ID_16583401,Human_RBP_ID_26561023 Human_miRNA_ID_659055 48852 RMVar_ID_48852 Human_SNP_ID_415867594 A-to-I Human chr9 - 128309254 128309254 128309254 CCAAGGCTGAGGCAGGAGAATTGCTTGAGCCCAGGAGTTTAAGGTTGTAGTGCGCTAGACGGCGC CCAAGGCTGAGGCAGGAGAATTGCTTGAGCCCGGGAGTTTAAGGTTGTAGTGCGCTAGACGGCGC T C TRUB2 Ensembl:ENSG00000167112 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs3180362 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8697279,Human_RBP_ID_16583403 Human_miRNA_ID_255965,Human_miRNA_ID_1159957 48853 RMVar_ID_48853 Human_SNP_ID_415870244 A-to-I Human chr9 - 128318985 128318985 128318985 TAGAGATGGGGTTTTGTCACGTTGCCCATGCTAGTATTGAACTCCTGGGCTCAAGTGATCTGCCT TAGAGATGGGGTTTTGTCACGTTGCCCATGCTCGTATTGAACTCCTGGGCTCAAGTGATCTGCCT T G TRUB2 Ensembl:ENSG00000167112 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1166798523 Functional Loss SNV dbSNP153 33..33 33 - - - 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 48854 RMVar_ID_48854 Human_SNP_ID_415871842 A-to-I Human chr9 + 128323699 128323699 128323699 CAGGCTAGGCGCTATTATAGTGGCTCACGCCTATAATCCCTATCGGGGGGCCGAAGCGGGCAGAT CAGGCTAGGCGCTATTATAGTGGCTCACGCCTGTAATCCCTATCGGGGGGCCGAAGCGGGCAGAT A G COQ4 Ensembl:ENSG00000167113 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1183304409 Functional Loss SNV dbSNP153 33..33 33 - - - 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 48855 RMVar_ID_48855 Human_SNP_ID_415872007 A-to-I Human chr9 + 128324297 128324297 128324297 CACCACGCCCGGCCAAGACCAGCGAATTTTTTAATTTTTTTGTAGAGACGGCGTCTTGCCACGTT CACCACGCCCGGCCAAGACCAGCGAATTTTTTTATTTTTTTGTAGAGACGGCGTCTTGCCACGTT A T COQ4 Ensembl:ENSG00000167113 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1266760528 Functional Loss SNV dbSNP153 33..33 33 - - - 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 48856 RMVar_ID_48856 Human_SNP_ID_415872603 A-to-I Human chr9 + 128326491 128326491 128326491 TTTTTTTTTTGAGTCGCTCTGTCGCCCAGGCTAGAGTGCAGTGGTGCGATCTCTGCTCACTGCAA TTTTTTTTTTGAGTCGCTCTGTCGCCCAGGCTGGAGTGCAGTGGTGCGATCTCTGCTCACTGCAA A G COQ4 Ensembl:ENSG00000167113 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1246964186 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96189,RMVar_hsa_circ_124412,RMVar_hsa_circ_259901,RMVar_hsa_circ_259902,RMVar_hsa_circ_81783,RMVar_hsa_circ_259905,RMVar_hsa_circ_259909,RMVar_hsa_circ_107447 48857 RMVar_ID_48857 Human_SNP_ID_415872641 A-to-I Human chr9 + 128326625 128326625 128326625 CCACGACGCCCGGCTAATTTTTTGTATTTTTTAGTAGAGACGGGGTTTCACCGTGCTAGCCAGGA CCACGACGCCCGGCTAATTTTTTGTATTTTTTCGTAGAGACGGGGTTTCACCGTGCTAGCCAGGA A C COQ4 Ensembl:ENSG00000167113 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1036489753 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96189,RMVar_hsa_circ_124412,RMVar_hsa_circ_259901,RMVar_hsa_circ_259902,RMVar_hsa_circ_81783,RMVar_hsa_circ_259905,RMVar_hsa_circ_259909,RMVar_hsa_circ_107447 48858 RMVar_ID_48858 Human_SNP_ID_415872642 A-to-I Human chr9 + 128326625 128326625 128326625 CCACGACGCCCGGCTAATTTTTTGTATTTTTTAGTAGAGACGGGGTTTCACCGTGCTAGCCAGGA CCACGACGCCCGGCTAATTTTTTGTATTTTTTGGTAGAGACGGGGTTTCACCGTGCTAGCCAGGA A G COQ4 Ensembl:ENSG00000167113 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1036489753 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96189,RMVar_hsa_circ_124412,RMVar_hsa_circ_259901,RMVar_hsa_circ_259902,RMVar_hsa_circ_81783,RMVar_hsa_circ_259905,RMVar_hsa_circ_259909,RMVar_hsa_circ_107447 48859 RMVar_ID_48859 Human_SNP_ID_415872669 A-to-I Human chr9 + 128326703 128326703 128326703 CTGACCACGTGATCCGCCCGCATCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACAGCG CTGACCACGTGATCCGCCCGCATCAGCCTCCCCAAGTGCTGGGATTACAGGCGTGAGCCACAGCG A C COQ4 Ensembl:ENSG00000167113 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs1304841123 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96189,RMVar_hsa_circ_124412,RMVar_hsa_circ_259901,RMVar_hsa_circ_259902,RMVar_hsa_circ_81783,RMVar_hsa_circ_259905,RMVar_hsa_circ_259909,RMVar_hsa_circ_107447 48860 RMVar_ID_48860 Human_SNP_ID_415872697 A-to-I Human chr9 + 128326789 128326789 128326789 TGTTTTGTTTTGAGACAGGGTCCCGCTCTGCCACCCAGGCTGGAGTGCAGTGGCGCCGTCTCGGC TGTTTTGTTTTGAGACAGGGTCCCGCTCTGCCGCCCAGGCTGGAGTGCAGTGGCGCCGTCTCGGC A G COQ4 Ensembl:ENSG00000167113 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1426601291 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16583611 RMVar_hsa_circ_96189,RMVar_hsa_circ_124412,RMVar_hsa_circ_259901,RMVar_hsa_circ_259902,RMVar_hsa_circ_81783,RMVar_hsa_circ_259905,RMVar_hsa_circ_259909,RMVar_hsa_circ_107447 48861 RMVar_ID_48861 Human_SNP_ID_415872744 A-to-I Human chr9 + 128326914 128326914 128326914 GGGACTACAGGTGCACACCACAACGCCCAGCTAATTTTTGTACTTTTAGTAGAGAGGGGTTTTAC GGGACTACAGGTGCACACCACAACGCCCAGCTGATTTTTGTACTTTTAGTAGAGAGGGGTTTTAC A G COQ4 Ensembl:ENSG00000167113 Protein coding intron GSE38233;GSE100210;GSE100210;GSE99789;GSE99789 cultured B-cells;HepG2 cell line;HepG2 cell line;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109 - 24183664,29129909,29129909,29796672,29796672 RNA-Seq:(High) rs1328435459 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96189,RMVar_hsa_circ_124412,RMVar_hsa_circ_259901,RMVar_hsa_circ_259902,RMVar_hsa_circ_81783,RMVar_hsa_circ_259905,RMVar_hsa_circ_259909,RMVar_hsa_circ_107447 48862 RMVar_ID_48862 Human_SNP_ID_415872894 A-to-I Human chr9 + 128327550 128327550 128327550 GTCCATGCGTGTTGGCTCATGCCTGTAATCCTAATACTTTGGGGGGCTGAAGTGGGCGGATCACT GTCCATGCGTGTTGGCTCATGCCTGTAATCCTGATACTTTGGGGGGCTGAAGTGGGCGGATCACT A G COQ4 Ensembl:ENSG00000167113 Protein coding intron GSE38233;GSE100210;GSE100210;GSE99789 cultured B-cells;HepG2 cell line;HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 24183664,29129909,29129909,29796672 RNA-Seq:(High) rs1304248486 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17579547 RMVar_hsa_circ_96189,RMVar_hsa_circ_124412,RMVar_hsa_circ_259901,RMVar_hsa_circ_259902,RMVar_hsa_circ_81783,RMVar_hsa_circ_259905,RMVar_hsa_circ_259909,RMVar_hsa_circ_107447 48863 RMVar_ID_48863 Human_SNP_ID_415872907 A-to-I Human chr9 + 128327590 128327590 128327590 GGGGGGCTGAAGTGGGCGGATCACTTGAGCCCAGGAGTTTGAGACCAGCCTGGACAACATGGTGA GGGGGGCTGAAGTGGGCGGATCACTTGAGCCCGGGAGTTTGAGACCAGCCTGGACAACATGGTGA A G COQ4 Ensembl:ENSG00000167113 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1029021324 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96189,RMVar_hsa_circ_124412,RMVar_hsa_circ_259901,RMVar_hsa_circ_259902,RMVar_hsa_circ_81783,RMVar_hsa_circ_259905,RMVar_hsa_circ_259909,RMVar_hsa_circ_107447 48864 RMVar_ID_48864 Human_SNP_ID_415872912 A-to-I Human chr9 + 128327613 128327613 128327613 CTTGAGCCCAGGAGTTTGAGACCAGCCTGGACAACATGGTGAAACCCTGTCTCTGCAAAAAATGC CTTGAGCCCAGGAGTTTGAGACCAGCCTGGACGACATGGTGAAACCCTGTCTCTGCAAAAAATGC A G COQ4 Ensembl:ENSG00000167113 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1257462923 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96189,RMVar_hsa_circ_124412,RMVar_hsa_circ_259901,RMVar_hsa_circ_259902,RMVar_hsa_circ_81783,RMVar_hsa_circ_259905,RMVar_hsa_circ_259909,RMVar_hsa_circ_107447 48865 RMVar_ID_48865 Human_SNP_ID_415872927 A-to-I Human chr9 + 128327679 128327679 128327679 AAAATTAGCCAAGTGTGGTGGTGTATACCCATAGTCCCAGCTACCTGGGAGGGAGTTTGAGGTAG AAAATTAGCCAAGTGTGGTGGTGTATACCCATCGTCCCAGCTACCTGGGAGGGAGTTTGAGGTAG A C COQ4 Ensembl:ENSG00000167113 Protein coding intron GSE47997;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,32596459 RNA-Seq:(High) rs1382481812 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96189,RMVar_hsa_circ_124412,RMVar_hsa_circ_259901,RMVar_hsa_circ_259902,RMVar_hsa_circ_81783,RMVar_hsa_circ_259905,RMVar_hsa_circ_259909,RMVar_hsa_circ_107447 48866 RMVar_ID_48866 Human_SNP_ID_415872951 A-to-I Human chr9 + 128327757 128327757 128327757 GCCCAGGAGGTCGAGGGCGGTGAGCCGTAATCACACCACTACACTCCAGCTTGGACAACAGAGCA GCCCAGGAGGTCGAGGGCGGTGAGCCGTAATCGCACCACTACACTCCAGCTTGGACAACAGAGCA A G COQ4 Ensembl:ENSG00000167113 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs141454823 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17579128,Human_RBP_ID_23090126 RMVar_hsa_circ_96189,RMVar_hsa_circ_124412,RMVar_hsa_circ_259901,RMVar_hsa_circ_259902,RMVar_hsa_circ_81783,RMVar_hsa_circ_259905,RMVar_hsa_circ_259909,RMVar_hsa_circ_107447 48867 RMVar_ID_48867 Human_SNP_ID_415872955 A-to-I Human chr9 + 128327765 128327765 128327765 GGTCGAGGGCGGTGAGCCGTAATCACACCACTACACTCCAGCTTGGACAACAGAGCAAGACTCTG GGTCGAGGGCGGTGAGCCGTAATCACACCACTGCACTCCAGCTTGGACAACAGAGCAAGACTCTG A G COQ4 Ensembl:ENSG00000167113 Protein coding intron GSE100210;GSE99789;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,EC109;ASD brains,frontal_cortex;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,29796672,30559470,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs1398556366 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17579128 RMVar_hsa_circ_96189,RMVar_hsa_circ_124412,RMVar_hsa_circ_259901,RMVar_hsa_circ_259902,RMVar_hsa_circ_81783,RMVar_hsa_circ_259905,RMVar_hsa_circ_259909,RMVar_hsa_circ_107447 48868 RMVar_ID_48868 Human_SNP_ID_415873356 A-to-I Human chr9 + 128329550 128329550 128329550 CGCCACCAGGCCTGGCTATTTTTTGTATTTTTAGTATAGGCGGGATTTCATCATATTGGCCAGGC CGCCACCAGGCCTGGCTATTTTTTGTATTTTTGGTATAGGCGGGATTTCATCATATTGGCCAGGC A G COQ4 Ensembl:ENSG00000167113 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1049386539 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16583714 RMVar_hsa_circ_96189,RMVar_hsa_circ_124412,RMVar_hsa_circ_259901,RMVar_hsa_circ_259902,RMVar_hsa_circ_81783,RMVar_hsa_circ_259905,RMVar_hsa_circ_259909,RMVar_hsa_circ_107447 48869 RMVar_ID_48869 Human_SNP_ID_415873537 A-to-I Human chr9 + 128330262 128330262 128330262 GGGTGTAGTGGCACGTGCCTGTAATCCTAGCTACTCAGGAAGCTGAGGCAGAAGAATTGCTTGAA GGGTGTAGTGGCACGTGCCTGTAATCCTAGCTGCTCAGGAAGCTGAGGCAGAAGAATTGCTTGAA A G COQ4 Ensembl:ENSG00000167113 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1315634401 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96189,RMVar_hsa_circ_124412,RMVar_hsa_circ_259901,RMVar_hsa_circ_259902,RMVar_hsa_circ_81783,RMVar_hsa_circ_259905,RMVar_hsa_circ_259909,RMVar_hsa_circ_107447 48870 RMVar_ID_48870 Human_SNP_ID_415873539 A-to-I Human chr9 + 128330266 128330266 128330266 GTAGTGGCACGTGCCTGTAATCCTAGCTACTCAGGAAGCTGAGGCAGAAGAATTGCTTGAATCCG GTAGTGGCACGTGCCTGTAATCCTAGCTACTCGGGAAGCTGAGGCAGAAGAATTGCTTGAATCCG A G COQ4 Ensembl:ENSG00000167113 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1228305459 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96189,RMVar_hsa_circ_124412,RMVar_hsa_circ_259901,RMVar_hsa_circ_259902,RMVar_hsa_circ_81783,RMVar_hsa_circ_259905,RMVar_hsa_circ_259909,RMVar_hsa_circ_107447 48871 RMVar_ID_48871 Human_SNP_ID_415873612 A-to-I Human chr9 + 128330517 128330517 128330517 AGGTGGAATTTTTTTGTTTGTTTTTTTGAGATAGAGTCTCACTCTGTTGCCCAGGCTGGAGTGCA AGGTGGAATTTTTTTGTTTGTTTTTTTGAGATGGAGTCTCACTCTGTTGCCCAGGCTGGAGTGCA A G COQ4 Ensembl:ENSG00000167113 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs1209775688 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96189,RMVar_hsa_circ_124412,RMVar_hsa_circ_259901,RMVar_hsa_circ_259902,RMVar_hsa_circ_81783,RMVar_hsa_circ_259905,RMVar_hsa_circ_259909,RMVar_hsa_circ_107447 48872 RMVar_ID_48872 Human_SNP_ID_415873626 A-to-I Human chr9 + 128330563 128330563 128330563 TTGCCCAGGCTGGAGTGCAATGGTGCCATCTCAGCTCACTGCAACCTCTGCCTTCTGGGATCAAG TTGCCCAGGCTGGAGTGCAATGGTGCCATCTCGGCTCACTGCAACCTCTGCCTTCTGGGATCAAG A G COQ4 Ensembl:ENSG00000167113 Protein coding intron GSE47997;GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,29129909,29796672,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs1174641338 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96189,RMVar_hsa_circ_124412,RMVar_hsa_circ_259901,RMVar_hsa_circ_259902,RMVar_hsa_circ_81783,RMVar_hsa_circ_259905,RMVar_hsa_circ_259909,RMVar_hsa_circ_107447 48873 RMVar_ID_48873 Human_SNP_ID_415873628 A-to-I Human chr9 + 128330568 128330568 128330568 CAGGCTGGAGTGCAATGGTGCCATCTCAGCTCACTGCAACCTCTGCCTTCTGGGATCAAGCAATT CAGGCTGGAGTGCAATGGTGCCATCTCAGCTCGCTGCAACCTCTGCCTTCTGGGATCAAGCAATT A G COQ4 Ensembl:ENSG00000167113 Protein coding intron GSE47997;GSE38233;GSE100210;GSE99789;GSE107867 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;ASD brains,Fragile X samples from NIH NeuroBioBank - 23474544,24183664,29129909,29796672,30559470 RNA-Seq:(High) rs1470353944 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96189,RMVar_hsa_circ_124412,RMVar_hsa_circ_259901,RMVar_hsa_circ_259902,RMVar_hsa_circ_81783,RMVar_hsa_circ_259905,RMVar_hsa_circ_259909,RMVar_hsa_circ_107447 48874 RMVar_ID_48874 Human_SNP_ID_415873630 A-to-I Human chr9 + 128330573 128330573 128330573 TGGAGTGCAATGGTGCCATCTCAGCTCACTGCAACCTCTGCCTTCTGGGATCAAGCAATTCTCTT TGGAGTGCAATGGTGCCATCTCAGCTCACTGCCACCTCTGCCTTCTGGGATCAAGCAATTCTCTT A C COQ4 Ensembl:ENSG00000167113 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1419238630 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96189,RMVar_hsa_circ_124412,RMVar_hsa_circ_259901,RMVar_hsa_circ_259902,RMVar_hsa_circ_81783,RMVar_hsa_circ_259905,RMVar_hsa_circ_259909,RMVar_hsa_circ_107447 48875 RMVar_ID_48875 Human_SNP_ID_415873651 A-to-I Human chr9 + 128330672 128330672 128330672 CCCGCCACCATGCCTGGCTAATTTTTGACCATATTGGTCAGGCTGGCCTTGAGCTCCTCAGGTGA CCCGCCACCATGCCTGGCTAATTTTTGACCATGTTGGTCAGGCTGGCCTTGAGCTCCTCAGGTGA A G COQ4 Ensembl:ENSG00000167113 Protein coding intron GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,29796672,31158229,31158229 RNA-Seq:(High) rs953873791 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16583746,Human_RBP_ID_23200154 RMVar_hsa_circ_96189,RMVar_hsa_circ_124412,RMVar_hsa_circ_259901,RMVar_hsa_circ_259902,RMVar_hsa_circ_81783,RMVar_hsa_circ_259905,RMVar_hsa_circ_259909,RMVar_hsa_circ_107447 48876 RMVar_ID_48876 Human_SNP_ID_415873757 A-to-I Human chr9 + 128330979 128330979 128330979 CCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCCGCCGCCACGCCCGGAGAATTTTTTG CCTGCCTCAGCCTCCCGAGTAGCTGGGACTACGGGCGCCCGCCGCCACGCCCGGAGAATTTTTTG A G COQ4 Ensembl:ENSG00000167113 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474781492 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96189,RMVar_hsa_circ_124412,RMVar_hsa_circ_259901,RMVar_hsa_circ_259902,RMVar_hsa_circ_81783,RMVar_hsa_circ_259905,RMVar_hsa_circ_259909,RMVar_hsa_circ_107447 48877 RMVar_ID_48877 Human_SNP_ID_415873913 A-to-I Human chr9 + 128331644 128331644 128331644 ATAGCTCCCTGTAACCTCAAACTCCTGGGCTCAAGCATCCTCCTGTCCCAAGCCTCCTGAGTAGC ATAGCTCCCTGTAACCTCAAACTCCTGGGCTCGAGCATCCTCCTGTCCCAAGCCTCCTGAGTAGC A G COQ4 Ensembl:ENSG00000167113 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1310198918 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16583788 RMVar_hsa_circ_96189,RMVar_hsa_circ_124412,RMVar_hsa_circ_259901,RMVar_hsa_circ_259902,RMVar_hsa_circ_81783,RMVar_hsa_circ_259905,RMVar_hsa_circ_259909,RMVar_hsa_circ_107447 48878 RMVar_ID_48878 Human_SNP_ID_415873922 A-to-I Human chr9 + 128331684 128331684 128331684 TCCTGTCCCAAGCCTCCTGAGTAGCTGGGACTATAGGCACACACCACCACACCTGACTAATTTTT TCCTGTCCCAAGCCTCCTGAGTAGCTGGGACTGTAGGCACACACCACCACACCTGACTAATTTTT A G COQ4 Ensembl:ENSG00000167113 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1195455217 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96189,RMVar_hsa_circ_124412,RMVar_hsa_circ_259901,RMVar_hsa_circ_259902,RMVar_hsa_circ_81783,RMVar_hsa_circ_259905,RMVar_hsa_circ_259909,RMVar_hsa_circ_107447 48879 RMVar_ID_48879 Human_SNP_ID_415873982 A-to-I Human chr9 + 128331912 128331912 128331912 ACCACACCCGGCTAATTTTTGTATTTTTTAGTAGAGACAGGGTTTCACCGTATTGGTCAGGCTGG ACCACACCCGGCTAATTTTTGTATTTTTTAGTGGAGACAGGGTTTCACCGTATTGGTCAGGCTGG A G COQ4 Ensembl:ENSG00000167113 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893775666 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17579380 RMVar_hsa_circ_96189,RMVar_hsa_circ_124412,RMVar_hsa_circ_259901,RMVar_hsa_circ_259902,RMVar_hsa_circ_81783,RMVar_hsa_circ_259905,RMVar_hsa_circ_259909,RMVar_hsa_circ_107447 48880 RMVar_ID_48880 Human_SNP_ID_415886232 A-to-I Human chr9 + 128375769 128375769 128375769 TTTTGTAGACACAAGGTGTTGCCATGTTGCCCAGGCTGCTCTTGAACTCCTGGACTTAAGCAATC TTTTGTAGACACAAGGTGTTGCCATGTTGCCCGGGCTGCTCTTGAACTCCTGGACTTAAGCAATC A G URM1 Ensembl:ENSG00000167118 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1300142644 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115758,RMVar_hsa_circ_259915 48881 RMVar_ID_48881 Human_SNP_ID_415886252 A-to-I Human chr9 + 128375824 128375824 128375824 TTAAGCAATCCTCCCTCGCCTCTCAGCCTCCCAAAGTGCTAGAGTTACAGGTGTGAGCCACTGTG TTAAGCAATCCTCCCTCGCCTCTCAGCCTCCCGAAGTGCTAGAGTTACAGGTGTGAGCCACTGTG A G URM1 Ensembl:ENSG00000167118 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs575097928 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115758,RMVar_hsa_circ_259915 48882 RMVar_ID_48882 Human_SNP_ID_415886253 A-to-I Human chr9 + 128375825 128375825 128375825 TAAGCAATCCTCCCTCGCCTCTCAGCCTCCCAAAGTGCTAGAGTTACAGGTGTGAGCCACTGTGT TAAGCAATCCTCCCTCGCCTCTCAGCCTCCCAGAGTGCTAGAGTTACAGGTGTGAGCCACTGTGT A G URM1 Ensembl:ENSG00000167118 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1222507794 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115758,RMVar_hsa_circ_259915 48883 RMVar_ID_48883 Human_SNP_ID_415886599 A-to-I Human chr9 + 128377140 128377140 128377140 GCAGTCATCTCGCCTTGGCCTCCCACAGTGCTAGGATTCCAGGTGTGAGCCACCACACCTAGCCG GCAGTCATCTCGCCTTGGCCTCCCACAGTGCTGGGATTCCAGGTGTGAGCCACCACACCTAGCCG A G URM1 Ensembl:ENSG00000167118 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947338838 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115758,RMVar_hsa_circ_259915 48884 RMVar_ID_48884 Human_SNP_ID_415887228 A-to-I Human chr9 + 128379270 128379270 128379270 TTGGGAGGCTGAGGCGGGCAGATCACGAGGTCAGGAGTTCCTGACCATCCTGATCAACATGATGA TTGGGAGGCTGAGGCGGGCAGATCACGAGGTCGGGAGTTCCTGACCATCCTGATCAACATGATGA A G URM1 Ensembl:ENSG00000167118 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1432936856 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115758,RMVar_hsa_circ_259915 48885 RMVar_ID_48885 Human_SNP_ID_415891397 A-to-I Human chr9 + 128395840 128395840 128395840 GCTCTGTCGCCCAGGCTGGAGTGCAGTGGCACAATCTCGGCTCACTGCAATCTCCACCAACTGCG GCTCTGTCGCCCAGGCTGGAGTGCAGTGGCACCATCTCGGCTCACTGCAATCTCCACCAACTGCG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs556885584 Functional Loss SNV dbSNP153 33..33 33 - - - 48886 RMVar_ID_48886 Human_SNP_ID_415891398 A-to-I Human chr9 + 128395840 128395840 128395840 GCTCTGTCGCCCAGGCTGGAGTGCAGTGGCACAATCTCGGCTCACTGCAATCTCCACCAACTGCG GCTCTGTCGCCCAGGCTGGAGTGCAGTGGCACGATCTCGGCTCACTGCAATCTCCACCAACTGCG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs556885584 Functional Loss SNV dbSNP153 33..33 33 - - - 48887 RMVar_ID_48887 Human_SNP_ID_415899591 A-to-I Human chr9 + 128426165 128426165 128426165 AAAATTAACTTGGCGTGTTGGCCCACGCCTGTAGTCCCAGCTTCCTGGGAGGCTGAGGCAGGAGG AAAATTAACTTGGCGTGTTGGCCCACGCCTGTGGTCCCAGCTTCCTGGGAGGCTGAGGCAGGAGG A G CERCAM Ensembl:ENSG00000167123 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1236461332 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7288,RMVar_hsa_circ_16358,RMVar_hsa_circ_349623,RMVar_hsa_circ_259924 48888 RMVar_ID_48888 Human_SNP_ID_415899947 A-to-I Human chr9 + 128427697 128427696 128427698 TGAGGCAGGAGAATTGCTCAAACCTGGGAGACAGAGGTTGTAATGAGCCAAGATCGCACCATTGC TGAGGCAGGAGAATTGCTCAAACCTGGGAGAC__AGGTTGTAATGAGCCAAGATCGCACCATTGC CAG C CERCAM Ensembl:ENSG00000167123 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1259654297 Functional Loss DEL dbSNP153 33..34 33 - - - Human_Splice_Rec_1086148,Human_Splice_Rec_1086149 RMVar_hsa_circ_7288,RMVar_hsa_circ_16358,RMVar_hsa_circ_349623,RMVar_hsa_circ_259924 48889 RMVar_ID_48889 Human_SNP_ID_415899954 A-to-I Human chr9 + 128427714 128427714 128427714 TCAAACCTGGGAGACAGAGGTTGTAATGAGCCAAGATCGCACCATTGCACTCCAGCCTCGGTGAC TCAAACCTGGGAGACAGAGGTTGTAATGAGCCGAGATCGCACCATTGCACTCCAGCCTCGGTGAC A G CERCAM Ensembl:ENSG00000167123 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1310448404 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1086148,Human_Splice_Rec_1086149 RMVar_hsa_circ_7288,RMVar_hsa_circ_16358,RMVar_hsa_circ_349623,RMVar_hsa_circ_259924 48890 RMVar_ID_48890 Human_SNP_ID_415909823 A-to-I Human chr9 + 128461548 128461548 128461548 TCAAGTGATTCTCCAGCCTCAGCCTCCCTAGTAGCTGGGACTACAGGCGCCCGCCACCACTTACG TCAAGTGATTCTCCAGCCTCAGCCTCCCTAGTTGCTGGGACTACAGGCGCCCGCCACCACTTACG A T ODF2 Ensembl:ENSG00000136811 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs998931853 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_584,RMVar_hsa_circ_37901,RMVar_hsa_circ_52451,RMVar_hsa_circ_57294,RMVar_hsa_circ_265966,RMVar_hsa_circ_268379 48891 RMVar_ID_48891 Human_SNP_ID_415910168 A-to-I Human chr9 + 128462765 128462765 128462765 GGGACTATAAGTGCCCGCCACCATGCCCGGCTAATTTTTTATGGTAGAGACGGGGTTTCACCGTG GGGACTATAAGTGCCCGCCACCATGCCCGGCTGATTTTTTATGGTAGAGACGGGGTTTCACCGTG A G ODF2 Ensembl:ENSG00000136811 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1361987835 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_584,RMVar_hsa_circ_37901,RMVar_hsa_circ_52451,RMVar_hsa_circ_57294,RMVar_hsa_circ_265966,RMVar_hsa_circ_268379 48892 RMVar_ID_48892 Human_SNP_ID_415910673 A-to-I Human chr9 + 128464640 128464640 128464640 TCCTGCCTCAGCCTCTGAGTTAGCTGGGACTCAGGCATGCACCACCACACCCAGCTAGTTTTTGT TCCTGCCTCAGCCTCTGAGTTAGCTGGGACTCGGGCATGCACCACCACACCCAGCTAGTTTTTGT A G ODF2 Ensembl:ENSG00000136811 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1208703997 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_584,RMVar_hsa_circ_37901,RMVar_hsa_circ_52451,RMVar_hsa_circ_57294,RMVar_hsa_circ_265966,RMVar_hsa_circ_268379 48893 RMVar_ID_48893 Human_SNP_ID_415911138 A-to-I Human chr9 + 128466399 128466399 128466399 TGAGGTGTAAGGATGGGTTGAGCCTGGGAGGCAGAGGTTGCAGTGAACCAAAGTTGTGCTACTGC TGAGGTGTAAGGATGGGTTGAGCCTGGGAGGCTGAGGTTGCAGTGAACCAAAGTTGTGCTACTGC A T ODF2 Ensembl:ENSG00000136811 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs558575645 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_584,RMVar_hsa_circ_37901,RMVar_hsa_circ_52451,RMVar_hsa_circ_57294,RMVar_hsa_circ_265966,RMVar_hsa_circ_268379 48894 RMVar_ID_48894 Human_SNP_ID_415912402 A-to-I Human chr9 + 128470373 128470373 128470373 CCCTTCTTGGCCAGGCGTGGTGGCTCATGCCTATAATCCTAGCACTTTGGGAGACTGAGGAGGGC CCCTTCTTGGCCAGGCGTGGTGGCTCATGCCTGTAATCCTAGCACTTTGGGAGACTGAGGAGGGC A G ODF2 Ensembl:ENSG00000136811 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs753130087 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_584,RMVar_hsa_circ_52451,RMVar_hsa_circ_57294,RMVar_hsa_circ_265966,RMVar_hsa_circ_268379,RMVar_hsa_circ_259932,RMVar_hsa_circ_34440,RMVar_hsa_circ_377976,RMVar_hsa_circ_329170,RMVar_hsa_circ_259933 48895 RMVar_ID_48895 Human_SNP_ID_415920427 A-to-I Human chr9 + 128502355 128502355 128502355 TTTTTTTGAAACAGGGTCTCCCTCTGTCATCCAAGCTGGTGAGCAGTGGCACAATGATGGCTCAC TTTTTTTGAAACAGGGTCTCCCTCTGTCATCCCAGCTGGTGAGCAGTGGCACAATGATGGCTCAC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285840983 Functional Loss SNV dbSNP153 33..33 33 - - - 48896 RMVar_ID_48896 Human_SNP_ID_415922450 A-to-I Human chr9 + 128509898 128509898 128509898 GGAGGATCACTTGAGCCCAGGAGTTTGAGACTACAGTGAGCTGTGATCAAGCCATTACATTCCAG GGAGGATCACTTGAGCCCAGGAGTTTGAGACTGCAGTGAGCTGTGATCAAGCCATTACATTCCAG A G GLE1 Ensembl:ENSG00000119392 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277163258 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124725,RMVar_hsa_circ_96495,RMVar_hsa_circ_284297,RMVar_hsa_circ_305835,RMVar_hsa_circ_329564,RMVar_hsa_circ_259942,RMVar_hsa_circ_313888,RMVar_hsa_circ_277414,RMVar_hsa_circ_28996,RMVar_hsa_circ_118679,RMVar_hsa_circ_120473,RMVar_hsa_circ_77995,RMVar_hsa_circ_259947,RMVar_hsa_circ_259949,RMVar_hsa_circ_259950,RMVar_hsa_circ_259951,RMVar_hsa_circ_259948,RMVar_hsa_circ_259945,RMVar_hsa_circ_259946,RMVar_hsa_circ_259944 48897 RMVar_ID_48897 Human_SNP_ID_415924164 A-to-I Human chr9 + 128515969 128515969 128515969 ATGGGACCTTAGCCTCTTTTTTTTTTTTTTTGAGGTGGAGTTTTTGCTCTTGTTGCCCAGGCTGG ATGGGACCTTAGCCTCTTTTTTTTTTTTTTTGTGGTGGAGTTTTTGCTCTTGTTGCCCAGGCTGG A T GLE1 Ensembl:ENSG00000119392 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560412373 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124725,RMVar_hsa_circ_305835,RMVar_hsa_circ_329564,RMVar_hsa_circ_313888,RMVar_hsa_circ_277414,RMVar_hsa_circ_28996,RMVar_hsa_circ_118679,RMVar_hsa_circ_120473,RMVar_hsa_circ_77995,RMVar_hsa_circ_259947,RMVar_hsa_circ_259949,RMVar_hsa_circ_259950,RMVar_hsa_circ_259951,RMVar_hsa_circ_259948,RMVar_hsa_circ_259945,RMVar_hsa_circ_259946,RMVar_hsa_circ_259952,RMVar_hsa_circ_115648 48898 RMVar_ID_48898 Human_SNP_ID_415924219 A-to-I Human chr9 + 128516218 128516218 128516218 GACCTCAGGTGATTCACCTGCCTCAGCCTCCCAAGGTGCTGGGATTACAGGCATGAGCCACGATG GACCTCAGGTGATTCACCTGCCTCAGCCTCCCTAGGTGCTGGGATTACAGGCATGAGCCACGATG A T GLE1 Ensembl:ENSG00000119392 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs10988013 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124725,RMVar_hsa_circ_305835,RMVar_hsa_circ_329564,RMVar_hsa_circ_313888,RMVar_hsa_circ_277414,RMVar_hsa_circ_28996,RMVar_hsa_circ_118679,RMVar_hsa_circ_120473,RMVar_hsa_circ_77995,RMVar_hsa_circ_259947,RMVar_hsa_circ_259949,RMVar_hsa_circ_259950,RMVar_hsa_circ_259951,RMVar_hsa_circ_259948,RMVar_hsa_circ_259945,RMVar_hsa_circ_259946,RMVar_hsa_circ_259952,RMVar_hsa_circ_115648 48899 RMVar_ID_48899 Human_SNP_ID_415924299 A-to-I Human chr9 + 128516526 128516526 128516526 TATTTTTAGTGGAGACAGGGTTTTGCCGTGTTAGCCAGGACGGTCTTGATCTTCTGACCTCGTGA TATTTTTAGTGGAGACAGGGTTTTGCCGTGTTTGCCAGGACGGTCTTGATCTTCTGACCTCGTGA A T GLE1 Ensembl:ENSG00000119392 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1435463204 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7900751,Human_RBP_ID_16584921 RMVar_hsa_circ_124725,RMVar_hsa_circ_305835,RMVar_hsa_circ_329564,RMVar_hsa_circ_313888,RMVar_hsa_circ_277414,RMVar_hsa_circ_28996,RMVar_hsa_circ_118679,RMVar_hsa_circ_120473,RMVar_hsa_circ_77995,RMVar_hsa_circ_259947,RMVar_hsa_circ_259949,RMVar_hsa_circ_259950,RMVar_hsa_circ_259951,RMVar_hsa_circ_259948,RMVar_hsa_circ_259945,RMVar_hsa_circ_259946,RMVar_hsa_circ_259952,RMVar_hsa_circ_115648 48900 RMVar_ID_48900 Human_SNP_ID_415924434 A-to-I Human chr9 + 128517057 128517040 128517058 CATGCCCGTAATCCCAGCACTTTGGGAGGGTGAGGCAGGTGGATCACCTGAGATAAGGAGTTCCA CATGCCCGTAATCCCA__________________GCAGGTGGATCACCTGAGATAAGGAGTTCCA AGCACTTTGGGAGGGTGAG A GLE1 Ensembl:ENSG00000119392 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1420048697 Functional Loss DEL dbSNP153 17..34 33 - - - RMVar_hsa_circ_124725,RMVar_hsa_circ_305835,RMVar_hsa_circ_329564,RMVar_hsa_circ_313888,RMVar_hsa_circ_277414,RMVar_hsa_circ_28996,RMVar_hsa_circ_118679,RMVar_hsa_circ_120473,RMVar_hsa_circ_77995,RMVar_hsa_circ_259947,RMVar_hsa_circ_259949,RMVar_hsa_circ_259950,RMVar_hsa_circ_259951,RMVar_hsa_circ_259948,RMVar_hsa_circ_259945,RMVar_hsa_circ_259946,RMVar_hsa_circ_259952,RMVar_hsa_circ_115648 48901 RMVar_ID_48901 Human_SNP_ID_415924443 A-to-I Human chr9 + 128517079 128517079 128517079 TGGGAGGGTGAGGCAGGTGGATCACCTGAGATAAGGAGTTCCAGACTGGCCTGGCCAACATGGCG TGGGAGGGTGAGGCAGGTGGATCACCTGAGATGAGGAGTTCCAGACTGGCCTGGCCAACATGGCG A G GLE1 Ensembl:ENSG00000119392 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1342412540 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124725,RMVar_hsa_circ_305835,RMVar_hsa_circ_329564,RMVar_hsa_circ_313888,RMVar_hsa_circ_277414,RMVar_hsa_circ_28996,RMVar_hsa_circ_118679,RMVar_hsa_circ_120473,RMVar_hsa_circ_77995,RMVar_hsa_circ_259947,RMVar_hsa_circ_259949,RMVar_hsa_circ_259950,RMVar_hsa_circ_259951,RMVar_hsa_circ_259948,RMVar_hsa_circ_259945,RMVar_hsa_circ_259946,RMVar_hsa_circ_259952,RMVar_hsa_circ_115648 48902 RMVar_ID_48902 Human_SNP_ID_415924465 A-to-I Human chr9 + 128517151 128517151 128517151 ATCTCTACTAAAAATACAAAAATTAGCCGGGCATGGTGGCACATGCCTATAATACTAGTTACTGG ATCTCTACTAAAAATACAAAAATTAGCCGGGCCTGGTGGCACATGCCTATAATACTAGTTACTGG A C GLE1 Ensembl:ENSG00000119392 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1480756769 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124725,RMVar_hsa_circ_305835,RMVar_hsa_circ_329564,RMVar_hsa_circ_313888,RMVar_hsa_circ_277414,RMVar_hsa_circ_28996,RMVar_hsa_circ_118679,RMVar_hsa_circ_120473,RMVar_hsa_circ_77995,RMVar_hsa_circ_259947,RMVar_hsa_circ_259949,RMVar_hsa_circ_259950,RMVar_hsa_circ_259951,RMVar_hsa_circ_259948,RMVar_hsa_circ_259945,RMVar_hsa_circ_259946,RMVar_hsa_circ_259952,RMVar_hsa_circ_115648 48903 RMVar_ID_48903 Human_SNP_ID_415927258 A-to-I Human chr9 + 128527808 128527808 128527808 CAACATAGTGAAACCCTGTCTCTACTAAAAATACAAATACTAGCTGGGTGTGGTGGCTCTCACCT CAACATAGTGAAACCCTGTCTCTACTAAAAATGCAAATACTAGCTGGGTGTGGTGGCTCTCACCT A G GLE1 Ensembl:ENSG00000119392 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs911316177 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124725,RMVar_hsa_circ_329564,RMVar_hsa_circ_28996,RMVar_hsa_circ_120473,RMVar_hsa_circ_259950,RMVar_hsa_circ_259951,RMVar_hsa_circ_259956,RMVar_hsa_circ_373474,RMVar_hsa_circ_320465,RMVar_hsa_circ_121615,RMVar_hsa_circ_259957,RMVar_hsa_circ_371751,RMVar_hsa_circ_259960,RMVar_hsa_circ_121063,RMVar_hsa_circ_342494,RMVar_hsa_circ_350507,RMVar_hsa_circ_259963 48904 RMVar_ID_48904 Human_SNP_ID_415927502 A-to-I Human chr9 + 128528555 128528555 128528555 TCGACCTCCTGACCTTGTGATCCGCCCGCCTCAGCTTCCCAAAGCGCTGGGATTACAGGCGTGAG TCGACCTCCTGACCTTGTGATCCGCCCGCCTCGGCTTCCCAAAGCGCTGGGATTACAGGCGTGAG A G GLE1 Ensembl:ENSG00000119392 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1263387277 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124725,RMVar_hsa_circ_329564,RMVar_hsa_circ_28996,RMVar_hsa_circ_120473,RMVar_hsa_circ_259950,RMVar_hsa_circ_259951,RMVar_hsa_circ_259956,RMVar_hsa_circ_373474,RMVar_hsa_circ_320465,RMVar_hsa_circ_121615,RMVar_hsa_circ_259957,RMVar_hsa_circ_371751,RMVar_hsa_circ_259960,RMVar_hsa_circ_121063,RMVar_hsa_circ_342494,RMVar_hsa_circ_350507,RMVar_hsa_circ_259963 48905 RMVar_ID_48905 Human_SNP_ID_415935701 A-to-I Human chr9 + 128560764 128560764 128560764 AGTGAAGGCCGGGTGCTGTGGCTCACGTCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGTGG AGTGAAGGCCGGGTGCTGTGGCTCACGTCTGTGATCCCAGCACTTTGGGAGGCTGAGGTGGGTGG A G SPTAN1 Ensembl:ENSG00000197694 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1163151086 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_259967,RMVar_hsa_circ_89021,RMVar_hsa_circ_122466,RMVar_hsa_circ_105437,RMVar_hsa_circ_259968,RMVar_hsa_circ_259969,RMVar_hsa_circ_259970,RMVar_hsa_circ_80231 48906 RMVar_ID_48906 Human_SNP_ID_415943801 A-to-I Human chr9 + 128590594 128590594 128590594 AAAAAAAGGGCCAGGCGTGGTGGTTCACGCCTATAATATCAGCGCTTTGGGAGGCTGAGGTGGGT AAAAAAAGGGCCAGGCGTGGTGGTTCACGCCTGTAATATCAGCGCTTTGGGAGGCTGAGGTGGGT A G SPTAN1 Ensembl:ENSG00000197694 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1003582358 Functional Loss SNV dbSNP153 33..33 33 - - - 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_259992,RMVar_hsa_circ_54178,RMVar_hsa_circ_259991 48907 RMVar_ID_48907 Human_SNP_ID_415943955 A-to-I Human chr9 + 128591203 128591203 128591203 CCTGCATCAGCCTCCCGAGTAGCTGGGGCTACAGGTGCCCACCACCATGTCCAGCTAATTTTTTT CCTGCATCAGCCTCCCGAGTAGCTGGGGCTACGGGTGCCCACCACCATGTCCAGCTAATTTTTTT A G SPTAN1 Ensembl:ENSG00000197694 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1248906492 Functional Loss SNV dbSNP153 33..33 33 - - - 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_259992,RMVar_hsa_circ_54178,RMVar_hsa_circ_259991 48908 RMVar_ID_48908 Human_SNP_ID_415945737 A-to-I Human chr9 + 128597853 128597853 128597853 TTGTATTTTTAGTAGAGACGGGGTTTCACCATATTGGCCCGGCTGGTCTTGGACTCCTGACCTCG TTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCCGGCTGGTCTTGGACTCCTGACCTCG A G SPTAN1 Ensembl:ENSG00000197694 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985851376 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16585368 RMVar_hsa_circ_655,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_4626,RMVar_hsa_circ_91821,RMVar_hsa_circ_259973,RMVar_hsa_circ_259975,RMVar_hsa_circ_107871,RMVar_hsa_circ_104104,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_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_54178,RMVar_hsa_circ_259991,RMVar_hsa_circ_358556,RMVar_hsa_circ_39558,RMVar_hsa_circ_265890 48909 RMVar_ID_48909 Human_SNP_ID_415952765 A-to-I Human chr9 + 128623812 128623812 128623812 TCTTTAGAATTAATTCCTTGGACCGGCTGGGCACTATGGCTCACACCTGTAATCCCAGCACTTTG TCTTTAGAATTAATTCCTTGGACCGGCTGGGCGCTATGGCTCACACCTGTAATCCCAGCACTTTG A G SPTAN1 Ensembl:ENSG00000197694 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1468885054 Functional Loss SNV dbSNP153 33..33 33 - - - 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_108877,RMVar_hsa_circ_259988,RMVar_hsa_circ_259991,RMVar_hsa_circ_265890,RMVar_hsa_circ_9604,RMVar_hsa_circ_259998,RMVar_hsa_circ_118989,RMVar_hsa_circ_259995,RMVar_hsa_circ_103220,RMVar_hsa_circ_123195,RMVar_hsa_circ_90880,RMVar_hsa_circ_100325,RMVar_hsa_circ_98058,RMVar_hsa_circ_89168,RMVar_hsa_circ_260000,RMVar_hsa_circ_260001,RMVar_hsa_circ_259999,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_76027,RMVar_hsa_circ_260025,RMVar_hsa_circ_260024,RMVar_hsa_circ_260031,RMVar_hsa_circ_108522,RMVar_hsa_circ_368859,RMVar_hsa_circ_126480,RMVar_hsa_circ_260037,RMVar_hsa_circ_90000,RMVar_hsa_circ_260041 48910 RMVar_ID_48910 Human_SNP_ID_415952809 A-to-I Human chr9 + 128623962 128623962 128623962 TAATTAGCTGTGCATGGTGGTGTTCGCCTATTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA TAATTAGCTGTGCATGGTGGTGTTCGCCTATTGGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA A G SPTAN1 Ensembl:ENSG00000197694 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1448205164 Functional Loss SNV dbSNP153 33..33 33 - - - 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_108877,RMVar_hsa_circ_259988,RMVar_hsa_circ_259991,RMVar_hsa_circ_265890,RMVar_hsa_circ_9604,RMVar_hsa_circ_259998,RMVar_hsa_circ_118989,RMVar_hsa_circ_259995,RMVar_hsa_circ_103220,RMVar_hsa_circ_123195,RMVar_hsa_circ_90880,RMVar_hsa_circ_100325,RMVar_hsa_circ_98058,RMVar_hsa_circ_89168,RMVar_hsa_circ_260000,RMVar_hsa_circ_260001,RMVar_hsa_circ_259999,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_76027,RMVar_hsa_circ_260025,RMVar_hsa_circ_260024,RMVar_hsa_circ_260031,RMVar_hsa_circ_108522,RMVar_hsa_circ_368859,RMVar_hsa_circ_126480,RMVar_hsa_circ_260037,RMVar_hsa_circ_90000,RMVar_hsa_circ_260041 48911 RMVar_ID_48911 Human_SNP_ID_415954954 A-to-I Human chr9 + 128631097 128630961 128631097 GAACTCCTGATCTCCAGTGATCTGTCCACCTCAGCCTCCCAAAGTGCTGGGATTACAAGCATGAG _________________________________GCCTCCCAAAGTGCTGGGATTACAAGCATGAG GGCCTCCCAAAGTGCTGGGATTACAAGCGTGAGCCACCACATCTGGCCTAGTTTTTATATTTTTAGTAGAGACAGTGTTTTGCCTTGTTGGCCAGGCCGGTCTGGAACTCCTGATCTCCAGTGATCTGTCCACCTCA G SPTAN1 Ensembl:ENSG00000197694 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1564327070 Functional Loss DEL dbSNP153 1..33 33 - - - 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_90080,RMVar_hsa_circ_260041,RMVar_hsa_circ_79030,RMVar_hsa_circ_260042,RMVar_hsa_circ_111172,RMVar_hsa_circ_260044,RMVar_hsa_circ_260045 48912 RMVar_ID_48912 Human_SNP_ID_415954970 A-to-I Human chr9 + 128631017 128631017 128631017 AAGCGTGAGCCACCACATCTGGCCTAGTTTTTATATTTTTAGTAGAGACAGTGTTTTGCCTTGTT AAGCGTGAGCCACCACATCTGGCCTAGTTTTTGTATTTTTAGTAGAGACAGTGTTTTGCCTTGTT A G SPTAN1 Ensembl:ENSG00000197694 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1258085071 Functional Loss SNV dbSNP153 33..33 33 - - - 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_90080,RMVar_hsa_circ_260041,RMVar_hsa_circ_79030,RMVar_hsa_circ_260042,RMVar_hsa_circ_111172,RMVar_hsa_circ_260044,RMVar_hsa_circ_260045 48913 RMVar_ID_48913 Human_SNP_ID_415954974 A-to-I Human chr9 + 128631034 128631034 128631034 TCTGGCCTAGTTTTTATATTTTTAGTAGAGACAGTGTTTTGCCTTGTTGGCCAGGCCGGTCTGGA TCTGGCCTAGTTTTTATATTTTTAGTAGAGACCGTGTTTTGCCTTGTTGGCCAGGCCGGTCTGGA A C SPTAN1 Ensembl:ENSG00000197694 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs530548615 Functional Loss SNV dbSNP153 33..33 33 - - - 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_90080,RMVar_hsa_circ_260041,RMVar_hsa_circ_79030,RMVar_hsa_circ_260042,RMVar_hsa_circ_111172,RMVar_hsa_circ_260044,RMVar_hsa_circ_260045 48914 RMVar_ID_48914 Human_SNP_ID_415955154 A-to-I Human chr9 - 128631744 128631744 128631744 GCAATCACGCTCACTGCAACCTCCCGGGTTCAAGTGATTCTCCTGCCTCAATCTCCTGAGTAGCT GCAATCACGCTCACTGCAACCTCCCGGGTTCAGGTGATTCTCCTGCCTCAATCTCCTGAGTAGCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1191810358 Functional Loss SNV dbSNP153 33..33 33 - - - 48915 RMVar_ID_48915 Human_SNP_ID_415955234 A-to-I Human chr9 + 128632018 128632018 128632018 CTATTCCTATTCTAGAATGTTCTTGTTTTACGAGGTCTCAGGCCAGGCCTGGAGCAGGAACCAGA CTATTCCTATTCTAGAATGTTCTTGTTTTACGGGGTCTCAGGCCAGGCCTGGAGCAGGAACCAGA A G SPTAN1 Ensembl:ENSG00000197694 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10760569 Functional Loss SNV dbSNP153 33..33 33 - - - 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_90080,RMVar_hsa_circ_260041,RMVar_hsa_circ_79030,RMVar_hsa_circ_260042,RMVar_hsa_circ_111172,RMVar_hsa_circ_260044,RMVar_hsa_circ_260045 48916 RMVar_ID_48916 Human_SNP_ID_415956096 A-to-I Human chr9 - 128633898 128633898 128633898 GATCAAGCAAACCCAGGATGAAAGCCCTGTCTACTGTCTGGAGTTCAACAGCCAGCAGACTCAGC GATCAAGCAAACCCAGGATGAAAGCCCTGTCTGCTGTCTGGAGTTCAACAGCCAGCAGACTCAGC T C WDR34 Ensembl:ENSG00000119333 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1564336534 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2061183,Human_RBP_ID_5011765,Human_RBP_ID_16585630,Human_RBP_ID_18904271,Human_RBP_ID_24287870,Human_RBP_ID_27542521 Human_Splice_Rec_1087540 Human_miRNA_ID_2585078,Human_miRNA_ID_2977046 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,RMVar_hsa_circ_260053 48917 RMVar_ID_48917 Human_SNP_ID_415957698 A-to-I Human chr9 - 128638080 128638080 128638080 GGCTCTGACCCCCATGCCCAGCTAATTTTTGTATTTTTGGTAGAGACGGGGTTTCACCATCTTGC GGCTCTGACCCCCATGCCCAGCTAATTTTTGTGTTTTTGGTAGAGACGGGGTTTCACCATCTTGC T C WDR34 Ensembl:ENSG00000119333 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1024455108 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84553,RMVar_hsa_circ_103594,RMVar_hsa_circ_260052,RMVar_hsa_circ_260051 48918 RMVar_ID_48918 Human_SNP_ID_415957706 A-to-I Human chr9 - 128638115 128638115 128638115 CTCCCACCTCAACTTCCTGAGTAGCTGGGATTACAGGCTCTGACCCCCATGCCCAGCTAATTTTT CTCCCACCTCAACTTCCTGAGTAGCTGGGATTGCAGGCTCTGACCCCCATGCCCAGCTAATTTTT T C WDR34 Ensembl:ENSG00000119333 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1488842665 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_84553,RMVar_hsa_circ_103594,RMVar_hsa_circ_260052,RMVar_hsa_circ_260051 48919 RMVar_ID_48919 Human_SNP_ID_415959257 A-to-I Human chr9 - 128643444 128643444 128643444 CGGCTCACTGCAACCTCCGCCCCCCAAGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGAGCAATT CGGCTCACTGCAACCTCCGCCCCCCAAGTTCAGGCGATTCTCCTGCCTCAGCCTCCTGAGCAATT T C WDR34 Ensembl:ENSG00000119333 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1372672130 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_103594,RMVar_hsa_circ_260052 48920 RMVar_ID_48920 Human_SNP_ID_415965346 A-to-I Human chr9 - 128664906 128664906 128664906 TTGCCCAGGCTGGTCTTGAACTCCTGAGCTCAAGTGCTCCTCCACCCTTAGGCCTTCCAAAGTGC TTGCCCAGGCTGGTCTTGAACTCCTGAGCTCACGTGCTCCTCCACCCTTAGGCCTTCCAAAGTGC T G HMGA1P4 Ensembl:ENSG00000234705 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1398362678 Functional Loss SNV dbSNP153 33..33 33 - - - 48921 RMVar_ID_48921 Human_SNP_ID_415965685 A-to-I Human chr9 - 128666159 128666159 128666159 GTTGGCCAGGCAGGTCTCGAACTGCTGACCTCAAGTGATCTGCCCGCCTTAGGCTCCCAAAGTTA GTTGGCCAGGCAGGTCTCGAACTGCTGACCTCCAGTGATCTGCCCGCCTTAGGCTCCCAAAGTTA T G HMGA1P4 Ensembl:ENSG00000234705 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1367569827 Functional Loss SNV dbSNP153 33..33 33 - - - 48922 RMVar_ID_48922 Human_SNP_ID_415965699 A-to-I Human chr9 - 128666213 128666213 128666213 CATGCCCACGCCCGGCTAACTTTTGTATTTTTAGTAGAGATGGGTTTTCTCCATGTTGGCCAGGC CATGCCCACGCCCGGCTAACTTTTGTATTTTTGGTAGAGATGGGTTTTCTCCATGTTGGCCAGGC T C HMGA1P4 Ensembl:ENSG00000234705 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs920389019 Functional Loss SNV dbSNP153 33..33 33 - - - 48923 RMVar_ID_48923 Human_SNP_ID_415966338 A-to-I Human chr9 - 128668125 128668125 128668125 GAAACCCCGTCTCTATTAAAAGTACAAAAATTAGCTGGGCATAGTGGCTCACGCCTGTAATCCCA GAAACCCCGTCTCTATTAAAAGTACAAAAATTGGCTGGGCATAGTGGCTCACGCCTGTAATCCCA T C HMGA1P4 Ensembl:ENSG00000234705 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1293202522 Functional Loss SNV dbSNP153 33..33 33 - - - 48924 RMVar_ID_48924 Human_SNP_ID_415968731 A-to-I Human chr9 - 128675950 128675950 128675950 TTACCCATGCTGGTCTTGAACTCCTAGACTCAAGTGATCCTCCTGCTTCAGCCTCCAGGGTAGCT TTACCCATGCTGGTCTTGAACTCCTAGACTCACGTGATCCTCCTGCTTCAGCCTCCAGGGTAGCT T G HMGA1P4 Ensembl:ENSG00000234705 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs544284151 Functional Loss SNV dbSNP153 33..33 33 - - - 48925 RMVar_ID_48925 Human_SNP_ID_415969884 A-to-I Human chr9 - 128680352 128680352 128680352 ATAATAATAATAATAATAATAATTGACCAGGTACAGTGGCTCATGCCTGTAATCCCAGCACTTTG ATAATAATAATAATAATAATAATTGACCAGGTGCAGTGGCTCATGCCTGTAATCCCAGCACTTTG T C HMGA1P4 Ensembl:ENSG00000234705 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1437613943 Functional Loss SNV dbSNP153 33..33 33 - - - 48926 RMVar_ID_48926 Human_SNP_ID_415970410 A-to-I Human chr9 - 128682232 128682232 128682232 CGTCCTGGCTAACACGGTGAAGCCCCACCTCTACTAAAAATACAAAAAATTAGCCGGGCGTGGTT CGTCCTGGCTAACACGGTGAAGCCCCACCTCTTCTAAAAATACAAAAAATTAGCCGGGCGTGGTT T A HMGA1P4 Ensembl:ENSG00000234705 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1197930184 Functional Loss SNV dbSNP153 33..33 33 - - - 48927 RMVar_ID_48927 Human_SNP_ID_415970498 A-to-I Human chr9 - 128682530 128682530 128682530 TGGGACTACAGACGTCACCACCATGCCTGGCTAATTTTTTGTATTTTTAGTAGGCACAGGGTTTG TGGGACTACAGACGTCACCACCATGCCTGGCTGATTTTTTGTATTTTTAGTAGGCACAGGGTTTG T C HMGA1P4 Ensembl:ENSG00000234705 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs61578139 Functional Loss SNV dbSNP153 33..33 33 - - - 48928 RMVar_ID_48928 Human_SNP_ID_415976194 A-to-I Human chr9 - 128698679 128698679 128698679 TCTCGAACTCCTGACCTTGTGAACACCCACTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG TCTCGAACTCCTGACCTTGTGAACACCCACTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG T C RF00017-071 RNACentral:URS00009310A4 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1313304853 Functional Loss SNV dbSNP153 33..33 33 - - - 48929 RMVar_ID_48929 Human_SNP_ID_415982069 A-to-I Human chr9 + 128717581 128717581 128717581 AAAATCTTGTCTCTACTAAAAATACAAAAATTAGCTAGGCATGGTGGCACACGCCTGTAATCCTA AAAATCTTGTCTCTACTAAAAATACAAAAATTGGCTAGGCATGGTGGCACACGCCTGTAATCCTA A G PKN3 Ensembl:ENSG00000160447 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1409680144 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6361,RMVar_hsa_circ_260071,RMVar_hsa_circ_103587,RMVar_hsa_circ_260073,RMVar_hsa_circ_310201 48930 RMVar_ID_48930 Human_SNP_ID_415982082 A-to-I Human chr9 + 128717629 128717629 128717629 ACACGCCTGTAATCCTAGCTACTTGAGAGGCTAAGGCAGGAGAATCGCTTGAACCCAGGAGGCGG ACACGCCTGTAATCCTAGCTACTTGAGAGGCTGAGGCAGGAGAATCGCTTGAACCCAGGAGGCGG A G PKN3 Ensembl:ENSG00000160447 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs146997426 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5923,GWAS_ID_5924 RMVar_hsa_circ_6361,RMVar_hsa_circ_260071,RMVar_hsa_circ_103587,RMVar_hsa_circ_260073,RMVar_hsa_circ_310201 48931 RMVar_ID_48931 Human_SNP_ID_415983212 A-to-I Human chr9 - 128720962 128720962 128720962 GAAAAGGACCTGTGGGTGGCTCAGGCCCAAGCAGACCCCGGGCTCCACCCCAGCCCCGCCCAGGC GAAAAGGACCTGTGGGTGGCTCAGGCCCAAGCCGACCCCGGGCTCCACCCCAGCCCCGCCCAGGC T G ZDHHC12 Ensembl:ENSG00000160446 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1274544046 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_712874 Human_miRNA_ID_475487,Human_miRNA_ID_1010400 48932 RMVar_ID_48932 Human_SNP_ID_415987010 A-to-I Human chr9 - 128734533 128734533 128734533 GCCCAAGAGGTTGAGACCAGCACAGGCAACACAGCGCAACCCTGTCTCTACTTAAAAAAAAAAAA GCCCAAGAGGTTGAGACCAGCACAGGCAACACGGCGCAACCCTGTCTCTACTTAAAAAAAAAAAA T C ZER1 Ensembl:ENSG00000160445 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs939784101 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_260076,RMVar_hsa_circ_114570,RMVar_hsa_circ_303359,RMVar_hsa_circ_345546,RMVar_hsa_circ_260077,RMVar_hsa_circ_351197,RMVar_hsa_circ_314214,RMVar_hsa_circ_260078 48933 RMVar_ID_48933 Human_SNP_ID_415987429 A-to-I Human chr9 - 128735902 128735902 128735902 GTGGTGGCACACCCCTGTAGTCTCAGTTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACCCA GTGGTGGCACACCCCTGTAGTCTCAGTTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCA T C ZER1 Ensembl:ENSG00000160445 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1287121650 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_62515,RMVar_hsa_circ_260076,RMVar_hsa_circ_114570,RMVar_hsa_circ_303359,RMVar_hsa_circ_351197,RMVar_hsa_circ_314214,RMVar_hsa_circ_260078 48934 RMVar_ID_48934 Human_SNP_ID_415990719 A-to-I Human chr9 - 128748495 128748495 128748495 ATGATCACAGCTCACTGTGGCCTCCACCTCTCAGGCTCAAGCAAGCCTCCCAACTCAGCCTCCCC ATGATCACAGCTCACTGTGGCCTCCACCTCTCGGGCTCAAGCAAGCCTCCCAACTCAGCCTCCCC T C ZER1 Ensembl:ENSG00000160445 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1176937192 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_260076,RMVar_hsa_circ_114570,RMVar_hsa_circ_303359,RMVar_hsa_circ_38157,RMVar_hsa_circ_260079,RMVar_hsa_circ_335771,RMVar_hsa_circ_91618,RMVar_hsa_circ_34180,RMVar_hsa_circ_87769,RMVar_hsa_circ_260081 48935 RMVar_ID_48935 Human_SNP_ID_416004490 A-to-I Human chr9 + 128801159 128801159 128801159 ACTCCATTGCACTCCAGCCTGGGTGACAGAGCAAGACTCCATCTCAAAAAAAGAAGAAGGGCATT ACTCCATTGCACTCCAGCCTGGGTGACAGAGCGAGACTCCATCTCAAAAAAAGAAGAAGGGCATT A G TBC1D13 Ensembl:ENSG00000107021 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs931624761 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125345,RMVar_hsa_circ_127318,RMVar_hsa_circ_260085,RMVar_hsa_circ_108681,RMVar_hsa_circ_260086,RMVar_hsa_circ_260087,RMVar_hsa_circ_297415,RMVar_hsa_circ_349335,RMVar_hsa_circ_260090 48936 RMVar_ID_48936 Human_SNP_ID_416016584 A-to-I Human chr9 - 128841483 128841483 128841483 CGCACTGTCGCCCCGGCTGGAGTCTGGAGTGCAGCGGCACGATCTCGGCTCACTGCAACCTCCGC CGCACTGTCGCCCCGGCTGGAGTCTGGAGTGCGGCGGCACGATCTCGGCTCACTGCAACCTCCGC T C AL441992.3,KYAT1 Ensembl:ENSG00000286112,Ensembl:ENSG00000171097 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs955972783 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16755633 RMVar_hsa_circ_56356,RMVar_hsa_circ_16220,RMVar_hsa_circ_36473,RMVar_hsa_circ_28626,RMVar_hsa_circ_305017,RMVar_hsa_circ_52654,RMVar_hsa_circ_295528,RMVar_hsa_circ_23063,RMVar_hsa_circ_21626,RMVar_hsa_circ_260102,RMVar_hsa_circ_35083 48937 RMVar_ID_48937 Human_SNP_ID_416018433 A-to-I Human chr9 - 128848559 128848559 128848559 CTCGCCTCAGCCTCCCACAGTGCTGGGATTACAGGCGTGAGCCACCATGCCTGGCCCCCATTTGA CTCGCCTCAGCCTCCCACAGTGCTGGGATTACGGGCGTGAGCCACCATGCCTGGCCCCCATTTGA T C AL441992.3,KYAT1 Ensembl:ENSG00000286112,Ensembl:ENSG00000171097 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348438695 Functional Loss SNV dbSNP153 33..33 33 - - - 48938 RMVar_ID_48938 Human_SNP_ID_416018749 A-to-I Human chr9 - 128849709 128849709 128849709 TCACTGCAACCTCCATCTCCCAAGTTGAAGCAATTCTCTGCCTCAGCCTCCTGAGTAGCTGGGAT TCACTGCAACCTCCATCTCCCAAGTTGAAGCAGTTCTCTGCCTCAGCCTCCTGAGTAGCTGGGAT T C AL441992.3,KYAT1 Ensembl:ENSG00000286112,Ensembl:ENSG00000171097 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1353343410 Functional Loss SNV dbSNP153 33..33 33 - - - 48939 RMVar_ID_48939 Human_SNP_ID_416018750 A-to-I Human chr9 - 128849710 128849710 128849710 CTCACTGCAACCTCCATCTCCCAAGTTGAAGCAATTCTCTGCCTCAGCCTCCTGAGTAGCTGGGA CTCACTGCAACCTCCATCTCCCAAGTTGAAGCTATTCTCTGCCTCAGCCTCCTGAGTAGCTGGGA T A AL441992.3,KYAT1 Ensembl:ENSG00000286112,Ensembl:ENSG00000171097 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1166166337 Functional Loss SNV dbSNP153 33..33 33 - - - 48940 RMVar_ID_48940 Human_SNP_ID_416021069 A-to-I Human chr9 - 128858840 128858840 128858840 CCATGTCCAGCTAATTTTTGTGTTGTTAGTACAGACAGGATTTCACCGTGTTGGCCAGTCTGGTC CCATGTCCAGCTAATTTTTGTGTTGTTAGTACGGACAGGATTTCACCGTGTTGGCCAGTCTGGTC T C AL441992.3,KYAT1 Ensembl:ENSG00000286112,Ensembl:ENSG00000171097 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1181676090 Functional Loss SNV dbSNP153 33..33 33 - - - 48941 RMVar_ID_48941 Human_SNP_ID_416021109 A-to-I Human chr9 - 128858972 128858972 128858972 TTTTTTTTTTTGAGATGGAGTCTTGTTCTGTCACCCAGGCTGGAGTGCAACGCACAATCTCAGCT TTTTTTTTTTTGAGATGGAGTCTTGTTCTGTCGCCCAGGCTGGAGTGCAACGCACAATCTCAGCT T C AL441992.3,KYAT1 Ensembl:ENSG00000286112,Ensembl:ENSG00000171097 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1411600622 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16587403 48942 RMVar_ID_48942 Human_SNP_ID_416021495 A-to-I Human chr9 - 128860623 128860623 128860623 AGGCGGAGCTTGCAGTGAGCCGAGATTGCGCAACTGCACTCCACCCTGGGCGACAAAGCAAGACT AGGCGGAGCTTGCAGTGAGCCGAGATTGCGCAGCTGCACTCCACCCTGGGCGACAAAGCAAGACT T C AL441992.3,KYAT1 Ensembl:ENSG00000286112,Ensembl:ENSG00000171097 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1419267536 Functional Loss SNV dbSNP153 33..33 33 - - - 48943 RMVar_ID_48943 Human_SNP_ID_416022136 A-to-I Human chr9 - 128863436 128863436 128863436 TAGAGAAAGGGTGTTGTTATGTTGCCCAGGCTAGTCTTGAACTTCTGAGCTCAAGCGATCTGCCC TAGAGAAAGGGTGTTGTTATGTTGCCCAGGCTGGTCTTGAACTTCTGAGCTCAAGCGATCTGCCC T C AL441992.3,KYAT1 Ensembl:ENSG00000286112,Ensembl:ENSG00000171097 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1486928087 Functional Loss SNV dbSNP153 33..33 33 - - - 48944 RMVar_ID_48944 Human_SNP_ID_416022529 A-to-I Human chr9 - 128864753 128864753 128864753 AATACAAAGATTAGCTGGACATGGTGGTGCACAACTGTAGTCCCAGCTACTCGGGAGGCTGAGGC AATACAAAGATTAGCTGGACATGGTGGTGCACGACTGTAGTCCCAGCTACTCGGGAGGCTGAGGC T C AL441992.3,KYAT1 Ensembl:ENSG00000286112,Ensembl:ENSG00000171097 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs955361331 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5410135 48945 RMVar_ID_48945 Human_SNP_ID_416023253 A-to-I Human chr9 - 128867255 128867255 128867255 GGATGGCTTGAGCCCCAGAGGTGTAAGCTGCAATGAGCCATAATTGTGCCACTGCACTCCAGACT GGATGGCTTGAGCCCCAGAGGTGTAAGCTGCAGTGAGCCATAATTGTGCCACTGCACTCCAGACT T C AL441992.3,KYAT1 Ensembl:ENSG00000286112,Ensembl:ENSG00000171097 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005364853 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16587495 48946 RMVar_ID_48946 Human_SNP_ID_416024087 A-to-I Human chr9 - 128870464 128870464 128870464 CCTGGCTGATTTTTGTATTTTTTGTAGAAACAAGGTTTTGCCGTGTTTCCCAGGCTGGTGTCAAA CCTGGCTGATTTTTGTATTTTTTGTAGAAACAGGGTTTTGCCGTGTTTCCCAGGCTGGTGTCAAA T C AL441992.3,KYAT1 Ensembl:ENSG00000286112,Ensembl:ENSG00000171097 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1447729174 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16587534 48947 RMVar_ID_48947 Human_SNP_ID_416024716 A-to-I Human chr9 - 128872822 128872822 128872822 GTGATCTGCCTGCCTCGGCCTCCCAAAGTTCTAGGATTACAGGCCTGAGCCACCACGTCTGGCCA GTGATCTGCCTGCCTCGGCCTCCCAAAGTTCTGGGATTACAGGCCTGAGCCACCACGTCTGGCCA T C AL441992.3,KYAT1 Ensembl:ENSG00000286112,Ensembl:ENSG00000171097 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1393688411 Functional Loss SNV dbSNP153 33..33 33 - - - 48948 RMVar_ID_48948 Human_SNP_ID_416026923 A-to-I Human chr9 - 128881287 128881287 128881287 CACGAGGTCAGGAGATCGAGACCATCCTGGCTAACTTGGTGAAACCTCATCTCTACTAAAAATAC CACGAGGTCAGGAGATCGAGACCATCCTGGCTCACTTGGTGAAACCTCATCTCTACTAAAAATAC T G AL441992.3,KYAT1 Ensembl:ENSG00000286112,Ensembl:ENSG00000171097 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935611099 Functional Loss SNV dbSNP153 33..33 33 - - - 48949 RMVar_ID_48949 Human_SNP_ID_416032956 A-to-I Human chr9 + 128905081 128905081 128905081 TGTAGCCCCAGCTACCTGGGGGAGGCTAAGGTAGGAGGATTGCTTGACCAGGAGGTTGAGGCTGC TGTAGCCCCAGCTACCTGGGGGAGGCTAAGGTGGGAGGATTGCTTGACCAGGAGGTTGAGGCTGC A G LRRC8A Ensembl:ENSG00000136802 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1262845986 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_105058,RMVar_hsa_circ_87431,RMVar_hsa_circ_260104,RMVar_hsa_circ_260105 48950 RMVar_ID_48950 Human_SNP_ID_416042335 A-to-I Human chr9 + 128939875 128939875 128939875 CAGGGTTTCACCATGTTGGCCAGGCTGGTCTCAAATTCCTGACCTCAGGTGATCCACCCGCCTTG CAGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAATTCCTGACCTCAGGTGATCCACCCGCCTTG A G PHYHD1 Ensembl:ENSG00000175287 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs113073633 Functional Loss SNV dbSNP153 33..33 33 - - - 48951 RMVar_ID_48951 Human_SNP_ID_416045752 A-to-I Human chr9 + 128950482 128950482 128950482 GCCTCAGGTGATCTGCCCACCTCAGTCTCCCAAAGTGCTTGGATTGCAGGCATGAGCCACTGTGC GCCTCAGGTGATCTGCCCACCTCAGTCTCCCAGAGTGCTTGGATTGCAGGCATGAGCCACTGTGC A G AL672142.1,NUP188 Ensembl:ENSG00000251184,Ensembl:ENSG00000095319 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs546563911 Functional Loss SNV dbSNP153 33..33 33 - - - 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_260109,RMVar_hsa_circ_14541,RMVar_hsa_circ_260110,RMVar_hsa_circ_260108 48952 RMVar_ID_48952 Human_SNP_ID_416050430 A-to-I Human chr9 + 128966489 128966489 128966489 GCCTTGACCTCCTGGGCTCAGGTAATCCTCCTACCTCAGCCTCCCAACTAGCTAGGACTACAAGA GCCTTGACCTCCTGGGCTCAGGTAATCCTCCTCCCTCAGCCTCCCAACTAGCTAGGACTACAAGA A C NUP188 Ensembl:ENSG00000095319 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1443480503 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24403,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_106140,RMVar_hsa_circ_34807,RMVar_hsa_circ_260109,RMVar_hsa_circ_14541,RMVar_hsa_circ_260110,RMVar_hsa_circ_264929,RMVar_hsa_circ_118940,RMVar_hsa_circ_303773,RMVar_hsa_circ_109413,RMVar_hsa_circ_260113,RMVar_hsa_circ_90036,RMVar_hsa_circ_97858,RMVar_hsa_circ_260115,RMVar_hsa_circ_260117,RMVar_hsa_circ_260116,RMVar_hsa_circ_260114,RMVar_hsa_circ_113915,RMVar_hsa_circ_260112,RMVar_hsa_circ_260119,RMVar_hsa_circ_120248,RMVar_hsa_circ_123975,RMVar_hsa_circ_125507,RMVar_hsa_circ_260121,RMVar_hsa_circ_260123,RMVar_hsa_circ_117786,RMVar_hsa_circ_260124,RMVar_hsa_circ_260122 48953 RMVar_ID_48953 Human_SNP_ID_416050431 A-to-I Human chr9 + 128966489 128966489 128966489 GCCTTGACCTCCTGGGCTCAGGTAATCCTCCTACCTCAGCCTCCCAACTAGCTAGGACTACAAGA GCCTTGACCTCCTGGGCTCAGGTAATCCTCCTGCCTCAGCCTCCCAACTAGCTAGGACTACAAGA A G NUP188 Ensembl:ENSG00000095319 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1443480503 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24403,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_106140,RMVar_hsa_circ_34807,RMVar_hsa_circ_260109,RMVar_hsa_circ_14541,RMVar_hsa_circ_260110,RMVar_hsa_circ_264929,RMVar_hsa_circ_118940,RMVar_hsa_circ_303773,RMVar_hsa_circ_109413,RMVar_hsa_circ_260113,RMVar_hsa_circ_90036,RMVar_hsa_circ_97858,RMVar_hsa_circ_260115,RMVar_hsa_circ_260117,RMVar_hsa_circ_260116,RMVar_hsa_circ_260114,RMVar_hsa_circ_113915,RMVar_hsa_circ_260112,RMVar_hsa_circ_260119,RMVar_hsa_circ_120248,RMVar_hsa_circ_123975,RMVar_hsa_circ_125507,RMVar_hsa_circ_260121,RMVar_hsa_circ_260123,RMVar_hsa_circ_117786,RMVar_hsa_circ_260124,RMVar_hsa_circ_260122 48954 RMVar_ID_48954 Human_SNP_ID_416053272 A-to-I Human chr9 + 128977676 128977676 128977676 CAGAGATGAGCTGGGCGTGGTGGTGGGCACCTATAATCCCAGTTACTCGGGATGCTGAGGCAGGA CAGAGATGAGCTGGGCGTGGTGGTGGGCACCTGTAATCCCAGTTACTCGGGATGCTGAGGCAGGA A G NUP188 Ensembl:ENSG00000095319 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs994671441 Functional Loss SNV dbSNP153 33..33 33 - - - 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_106140,RMVar_hsa_circ_34807,RMVar_hsa_circ_260109,RMVar_hsa_circ_260110,RMVar_hsa_circ_264929,RMVar_hsa_circ_118940,RMVar_hsa_circ_303773,RMVar_hsa_circ_109413,RMVar_hsa_circ_260113,RMVar_hsa_circ_90036,RMVar_hsa_circ_97858,RMVar_hsa_circ_260115,RMVar_hsa_circ_260117,RMVar_hsa_circ_260116,RMVar_hsa_circ_260114,RMVar_hsa_circ_113915,RMVar_hsa_circ_260112,RMVar_hsa_circ_260119,RMVar_hsa_circ_10585,RMVar_hsa_circ_120248,RMVar_hsa_circ_123975,RMVar_hsa_circ_125507,RMVar_hsa_circ_260121,RMVar_hsa_circ_82302,RMVar_hsa_circ_260123,RMVar_hsa_circ_117786,RMVar_hsa_circ_260124,RMVar_hsa_circ_335125,RMVar_hsa_circ_260122,RMVar_hsa_circ_260125,RMVar_hsa_circ_260126,RMVar_hsa_circ_290680,RMVar_hsa_circ_338378,RMVar_hsa_circ_103988,RMVar_hsa_circ_260133,RMVar_hsa_circ_86984,RMVar_hsa_circ_94522,RMVar_hsa_circ_260135,RMVar_hsa_circ_84664,RMVar_hsa_circ_260134,RMVar_hsa_circ_260131,RMVar_hsa_circ_260132,RMVar_hsa_circ_119336,RMVar_hsa_circ_324599,RMVar_hsa_circ_356763,RMVar_hsa_circ_89356,RMVar_hsa_circ_117645,RMVar_hsa_circ_260136,RMVar_hsa_circ_260138,RMVar_hsa_circ_260137,RMVar_hsa_circ_121481,RMVar_hsa_circ_295014,RMVar_hsa_circ_260141,RMVar_hsa_circ_111986,RMVar_hsa_circ_260142,RMVar_hsa_circ_260140 48955 RMVar_ID_48955 Human_SNP_ID_416053606 A-to-I Human chr9 + 128978894 128978894 128978894 CACCACACCTGGCTAACTTTCGTATTTTTAGTAGACATGGGGTTTCACCATGTTGGCCAGGCTGG CACCACACCTGGCTAACTTTCGTATTTTTAGTGGACATGGGGTTTCACCATGTTGGCCAGGCTGG A G NUP188 Ensembl:ENSG00000095319 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs552983189 Functional Loss SNV dbSNP153 33..33 33 - - - 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_106140,RMVar_hsa_circ_34807,RMVar_hsa_circ_260109,RMVar_hsa_circ_260110,RMVar_hsa_circ_264929,RMVar_hsa_circ_118940,RMVar_hsa_circ_303773,RMVar_hsa_circ_109413,RMVar_hsa_circ_260113,RMVar_hsa_circ_90036,RMVar_hsa_circ_97858,RMVar_hsa_circ_260115,RMVar_hsa_circ_260117,RMVar_hsa_circ_260116,RMVar_hsa_circ_260114,RMVar_hsa_circ_113915,RMVar_hsa_circ_260112,RMVar_hsa_circ_260119,RMVar_hsa_circ_10585,RMVar_hsa_circ_120248,RMVar_hsa_circ_123975,RMVar_hsa_circ_125507,RMVar_hsa_circ_260121,RMVar_hsa_circ_82302,RMVar_hsa_circ_260123,RMVar_hsa_circ_117786,RMVar_hsa_circ_260124,RMVar_hsa_circ_335125,RMVar_hsa_circ_260122,RMVar_hsa_circ_260125,RMVar_hsa_circ_260126,RMVar_hsa_circ_290680,RMVar_hsa_circ_338378,RMVar_hsa_circ_103988,RMVar_hsa_circ_260133,RMVar_hsa_circ_86984,RMVar_hsa_circ_94522,RMVar_hsa_circ_260135,RMVar_hsa_circ_84664,RMVar_hsa_circ_260134,RMVar_hsa_circ_260131,RMVar_hsa_circ_260132,RMVar_hsa_circ_119336,RMVar_hsa_circ_324599,RMVar_hsa_circ_356763,RMVar_hsa_circ_89356,RMVar_hsa_circ_117645,RMVar_hsa_circ_260136,RMVar_hsa_circ_260138,RMVar_hsa_circ_260137,RMVar_hsa_circ_121481,RMVar_hsa_circ_295014,RMVar_hsa_circ_260141,RMVar_hsa_circ_111986,RMVar_hsa_circ_260142,RMVar_hsa_circ_260140 48956 RMVar_ID_48956 Human_SNP_ID_416056465 A-to-I Human chr9 + 128988826 128988826 128988826 TCGGCTTACTGCAGCATCTGCCTCCTGGGTTTAAGCAATCCTCCTGCCTCAGCTTCCCGAGTAGC TCGGCTTACTGCAGCATCTGCCTCCTGGGTTTCAGCAATCCTCCTGCCTCAGCTTCCCGAGTAGC A C NUP188 Ensembl:ENSG00000095319 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978171210 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20344,RMVar_hsa_circ_264929,RMVar_hsa_circ_10585,RMVar_hsa_circ_125507,RMVar_hsa_circ_82302,RMVar_hsa_circ_260123,RMVar_hsa_circ_117786,RMVar_hsa_circ_260124,RMVar_hsa_circ_260125,RMVar_hsa_circ_86984,RMVar_hsa_circ_260135,RMVar_hsa_circ_117645,RMVar_hsa_circ_260142,RMVar_hsa_circ_108518,RMVar_hsa_circ_127255,RMVar_hsa_circ_108464,RMVar_hsa_circ_94885,RMVar_hsa_circ_83943,RMVar_hsa_circ_91598,RMVar_hsa_circ_84257,RMVar_hsa_circ_78164,RMVar_hsa_circ_83871,RMVar_hsa_circ_88950,RMVar_hsa_circ_260145,RMVar_hsa_circ_260149,RMVar_hsa_circ_260151,RMVar_hsa_circ_260152,RMVar_hsa_circ_260150,RMVar_hsa_circ_260147,RMVar_hsa_circ_260148,RMVar_hsa_circ_260146,RMVar_hsa_circ_260144,RMVar_hsa_circ_109440,RMVar_hsa_circ_260160,RMVar_hsa_circ_99400,RMVar_hsa_circ_81218,RMVar_hsa_circ_260158,RMVar_hsa_circ_260159,RMVar_hsa_circ_98205,RMVar_hsa_circ_113261,RMVar_hsa_circ_76421,RMVar_hsa_circ_119813,RMVar_hsa_circ_260169,RMVar_hsa_circ_260170,RMVar_hsa_circ_260171,RMVar_hsa_circ_348143,RMVar_hsa_circ_260174,RMVar_hsa_circ_95266,RMVar_hsa_circ_260172,RMVar_hsa_circ_260173,RMVar_hsa_circ_260179 48957 RMVar_ID_48957 Human_SNP_ID_416056495 A-to-I Human chr9 + 128988955 128988955 128988955 TTTGTTCTGTTTGGTAGAGACGAGCTTTCGCTATGTTGGCCAGGCTGGTCTCGAACTCCTGACCT TTTGTTCTGTTTGGTAGAGACGAGCTTTCGCTCTGTTGGCCAGGCTGGTCTCGAACTCCTGACCT A C NUP188 Ensembl:ENSG00000095319 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285413007 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20344,RMVar_hsa_circ_264929,RMVar_hsa_circ_10585,RMVar_hsa_circ_125507,RMVar_hsa_circ_82302,RMVar_hsa_circ_260123,RMVar_hsa_circ_117786,RMVar_hsa_circ_260124,RMVar_hsa_circ_260125,RMVar_hsa_circ_86984,RMVar_hsa_circ_260135,RMVar_hsa_circ_117645,RMVar_hsa_circ_260142,RMVar_hsa_circ_108518,RMVar_hsa_circ_127255,RMVar_hsa_circ_108464,RMVar_hsa_circ_94885,RMVar_hsa_circ_83943,RMVar_hsa_circ_91598,RMVar_hsa_circ_84257,RMVar_hsa_circ_78164,RMVar_hsa_circ_83871,RMVar_hsa_circ_88950,RMVar_hsa_circ_260145,RMVar_hsa_circ_260149,RMVar_hsa_circ_260151,RMVar_hsa_circ_260152,RMVar_hsa_circ_260150,RMVar_hsa_circ_260147,RMVar_hsa_circ_260148,RMVar_hsa_circ_260146,RMVar_hsa_circ_260144,RMVar_hsa_circ_109440,RMVar_hsa_circ_260160,RMVar_hsa_circ_99400,RMVar_hsa_circ_81218,RMVar_hsa_circ_260158,RMVar_hsa_circ_260159,RMVar_hsa_circ_98205,RMVar_hsa_circ_113261,RMVar_hsa_circ_76421,RMVar_hsa_circ_119813,RMVar_hsa_circ_260169,RMVar_hsa_circ_260170,RMVar_hsa_circ_260171,RMVar_hsa_circ_348143,RMVar_hsa_circ_260174,RMVar_hsa_circ_95266,RMVar_hsa_circ_260172,RMVar_hsa_circ_260173,RMVar_hsa_circ_260179 48958 RMVar_ID_48958 Human_SNP_ID_416056496 A-to-I Human chr9 + 128988955 128988955 128988955 TTTGTTCTGTTTGGTAGAGACGAGCTTTCGCTATGTTGGCCAGGCTGGTCTCGAACTCCTGACCT TTTGTTCTGTTTGGTAGAGACGAGCTTTCGCTGTGTTGGCCAGGCTGGTCTCGAACTCCTGACCT A G NUP188 Ensembl:ENSG00000095319 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285413007 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20344,RMVar_hsa_circ_264929,RMVar_hsa_circ_10585,RMVar_hsa_circ_125507,RMVar_hsa_circ_82302,RMVar_hsa_circ_260123,RMVar_hsa_circ_117786,RMVar_hsa_circ_260124,RMVar_hsa_circ_260125,RMVar_hsa_circ_86984,RMVar_hsa_circ_260135,RMVar_hsa_circ_117645,RMVar_hsa_circ_260142,RMVar_hsa_circ_108518,RMVar_hsa_circ_127255,RMVar_hsa_circ_108464,RMVar_hsa_circ_94885,RMVar_hsa_circ_83943,RMVar_hsa_circ_91598,RMVar_hsa_circ_84257,RMVar_hsa_circ_78164,RMVar_hsa_circ_83871,RMVar_hsa_circ_88950,RMVar_hsa_circ_260145,RMVar_hsa_circ_260149,RMVar_hsa_circ_260151,RMVar_hsa_circ_260152,RMVar_hsa_circ_260150,RMVar_hsa_circ_260147,RMVar_hsa_circ_260148,RMVar_hsa_circ_260146,RMVar_hsa_circ_260144,RMVar_hsa_circ_109440,RMVar_hsa_circ_260160,RMVar_hsa_circ_99400,RMVar_hsa_circ_81218,RMVar_hsa_circ_260158,RMVar_hsa_circ_260159,RMVar_hsa_circ_98205,RMVar_hsa_circ_113261,RMVar_hsa_circ_76421,RMVar_hsa_circ_119813,RMVar_hsa_circ_260169,RMVar_hsa_circ_260170,RMVar_hsa_circ_260171,RMVar_hsa_circ_348143,RMVar_hsa_circ_260174,RMVar_hsa_circ_95266,RMVar_hsa_circ_260172,RMVar_hsa_circ_260173,RMVar_hsa_circ_260179 48959 RMVar_ID_48959 Human_SNP_ID_416056542 A-to-I Human chr9 + 128989214 128989214 128989214 GTCCAGGAGTTCGAGACCAGCTTGGGCAAAATAAGGAGACCTCCATCTATACCAAAACAAACAAA GTCCAGGAGTTCGAGACCAGCTTGGGCAAAATGAGGAGACCTCCATCTATACCAAAACAAACAAA A G NUP188 Ensembl:ENSG00000095319 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs542857170 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17579710 RMVar_hsa_circ_20344,RMVar_hsa_circ_264929,RMVar_hsa_circ_10585,RMVar_hsa_circ_125507,RMVar_hsa_circ_82302,RMVar_hsa_circ_260123,RMVar_hsa_circ_117786,RMVar_hsa_circ_260124,RMVar_hsa_circ_260125,RMVar_hsa_circ_86984,RMVar_hsa_circ_260135,RMVar_hsa_circ_117645,RMVar_hsa_circ_260142,RMVar_hsa_circ_108518,RMVar_hsa_circ_127255,RMVar_hsa_circ_108464,RMVar_hsa_circ_94885,RMVar_hsa_circ_83943,RMVar_hsa_circ_91598,RMVar_hsa_circ_84257,RMVar_hsa_circ_78164,RMVar_hsa_circ_83871,RMVar_hsa_circ_88950,RMVar_hsa_circ_260145,RMVar_hsa_circ_260149,RMVar_hsa_circ_260151,RMVar_hsa_circ_260152,RMVar_hsa_circ_260150,RMVar_hsa_circ_260147,RMVar_hsa_circ_260148,RMVar_hsa_circ_260146,RMVar_hsa_circ_260144,RMVar_hsa_circ_109440,RMVar_hsa_circ_260160,RMVar_hsa_circ_99400,RMVar_hsa_circ_81218,RMVar_hsa_circ_260158,RMVar_hsa_circ_260159,RMVar_hsa_circ_98205,RMVar_hsa_circ_113261,RMVar_hsa_circ_76421,RMVar_hsa_circ_119813,RMVar_hsa_circ_260169,RMVar_hsa_circ_260170,RMVar_hsa_circ_260171,RMVar_hsa_circ_348143,RMVar_hsa_circ_260174,RMVar_hsa_circ_95266,RMVar_hsa_circ_260172,RMVar_hsa_circ_260173,RMVar_hsa_circ_260179 48960 RMVar_ID_48960 Human_SNP_ID_416057134 A-to-I Human chr9 + 128991311 128991311 128991311 CCTGTAATCCCAGTACTTTGGGAGGCTGAAGCAGGTGGATCATGAGGTCAGGGGTTCAAGACCAG CCTGTAATCCCAGTACTTTGGGAGGCTGAAGCGGGTGGATCATGAGGTCAGGGGTTCAAGACCAG A G NUP188 Ensembl:ENSG00000095319 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1220344784 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20344,RMVar_hsa_circ_264929,RMVar_hsa_circ_125507,RMVar_hsa_circ_82302,RMVar_hsa_circ_260123,RMVar_hsa_circ_117786,RMVar_hsa_circ_260124,RMVar_hsa_circ_260125,RMVar_hsa_circ_86984,RMVar_hsa_circ_260135,RMVar_hsa_circ_117645,RMVar_hsa_circ_260142,RMVar_hsa_circ_108518,RMVar_hsa_circ_127255,RMVar_hsa_circ_108464,RMVar_hsa_circ_94885,RMVar_hsa_circ_83943,RMVar_hsa_circ_91598,RMVar_hsa_circ_84257,RMVar_hsa_circ_78164,RMVar_hsa_circ_83871,RMVar_hsa_circ_88950,RMVar_hsa_circ_260145,RMVar_hsa_circ_260149,RMVar_hsa_circ_260151,RMVar_hsa_circ_260152,RMVar_hsa_circ_260150,RMVar_hsa_circ_260147,RMVar_hsa_circ_260148,RMVar_hsa_circ_260146,RMVar_hsa_circ_260144,RMVar_hsa_circ_109440,RMVar_hsa_circ_260160,RMVar_hsa_circ_99400,RMVar_hsa_circ_81218,RMVar_hsa_circ_260158,RMVar_hsa_circ_260159,RMVar_hsa_circ_98205,RMVar_hsa_circ_113261,RMVar_hsa_circ_76421,RMVar_hsa_circ_119813,RMVar_hsa_circ_260169,RMVar_hsa_circ_260170,RMVar_hsa_circ_260171,RMVar_hsa_circ_95266,RMVar_hsa_circ_260172,RMVar_hsa_circ_260173,RMVar_hsa_circ_260180,RMVar_hsa_circ_113549,RMVar_hsa_circ_302177,RMVar_hsa_circ_373558,RMVar_hsa_circ_260179,RMVar_hsa_circ_315907,RMVar_hsa_circ_282031,RMVar_hsa_circ_260182,RMVar_hsa_circ_260183,RMVar_hsa_circ_260184,RMVar_hsa_circ_260181 48961 RMVar_ID_48961 Human_SNP_ID_416057377 A-to-I Human chr9 + 128992157 128992157 128992157 CTGACCTCGTGATCTGCCCGCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCGC CTGACCTCGTGATCTGCCCGCTTGGCCTCCCAGAGTGCTGGGATTACAGGCATGAGCCACCGCGC A G NUP188 Ensembl:ENSG00000095319 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs141801301 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20344,RMVar_hsa_circ_264929,RMVar_hsa_circ_125507,RMVar_hsa_circ_82302,RMVar_hsa_circ_260123,RMVar_hsa_circ_117786,RMVar_hsa_circ_260124,RMVar_hsa_circ_260125,RMVar_hsa_circ_86984,RMVar_hsa_circ_260135,RMVar_hsa_circ_117645,RMVar_hsa_circ_260142,RMVar_hsa_circ_108518,RMVar_hsa_circ_127255,RMVar_hsa_circ_108464,RMVar_hsa_circ_94885,RMVar_hsa_circ_83943,RMVar_hsa_circ_91598,RMVar_hsa_circ_84257,RMVar_hsa_circ_78164,RMVar_hsa_circ_83871,RMVar_hsa_circ_88950,RMVar_hsa_circ_260145,RMVar_hsa_circ_260149,RMVar_hsa_circ_260151,RMVar_hsa_circ_260152,RMVar_hsa_circ_260150,RMVar_hsa_circ_260147,RMVar_hsa_circ_260148,RMVar_hsa_circ_260146,RMVar_hsa_circ_260144,RMVar_hsa_circ_109440,RMVar_hsa_circ_260160,RMVar_hsa_circ_99400,RMVar_hsa_circ_81218,RMVar_hsa_circ_260158,RMVar_hsa_circ_260159,RMVar_hsa_circ_98205,RMVar_hsa_circ_113261,RMVar_hsa_circ_76421,RMVar_hsa_circ_119813,RMVar_hsa_circ_260169,RMVar_hsa_circ_260170,RMVar_hsa_circ_260171,RMVar_hsa_circ_95266,RMVar_hsa_circ_260172,RMVar_hsa_circ_260173,RMVar_hsa_circ_260180,RMVar_hsa_circ_113549,RMVar_hsa_circ_302177,RMVar_hsa_circ_373558,RMVar_hsa_circ_260179,RMVar_hsa_circ_315907,RMVar_hsa_circ_282031,RMVar_hsa_circ_260182,RMVar_hsa_circ_260183,RMVar_hsa_circ_260184,RMVar_hsa_circ_260181 48962 RMVar_ID_48962 Human_SNP_ID_416057390 A-to-I Human chr9 + 128992222 128992222 128992222 CCAGCCCTTCCTGGTACTGTTTTTGTTTTGAGACAGTCCCACTCCATCACCCAGGCTGGAGTGCT CCAGCCCTTCCTGGTACTGTTTTTGTTTTGAGGCAGTCCCACTCCATCACCCAGGCTGGAGTGCT A G NUP188 Ensembl:ENSG00000095319 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs977393699 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20344,RMVar_hsa_circ_264929,RMVar_hsa_circ_125507,RMVar_hsa_circ_82302,RMVar_hsa_circ_260123,RMVar_hsa_circ_117786,RMVar_hsa_circ_260124,RMVar_hsa_circ_260125,RMVar_hsa_circ_86984,RMVar_hsa_circ_260135,RMVar_hsa_circ_117645,RMVar_hsa_circ_260142,RMVar_hsa_circ_108518,RMVar_hsa_circ_127255,RMVar_hsa_circ_108464,RMVar_hsa_circ_94885,RMVar_hsa_circ_83943,RMVar_hsa_circ_91598,RMVar_hsa_circ_84257,RMVar_hsa_circ_78164,RMVar_hsa_circ_83871,RMVar_hsa_circ_88950,RMVar_hsa_circ_260145,RMVar_hsa_circ_260149,RMVar_hsa_circ_260151,RMVar_hsa_circ_260152,RMVar_hsa_circ_260150,RMVar_hsa_circ_260147,RMVar_hsa_circ_260148,RMVar_hsa_circ_260146,RMVar_hsa_circ_260144,RMVar_hsa_circ_109440,RMVar_hsa_circ_260160,RMVar_hsa_circ_99400,RMVar_hsa_circ_81218,RMVar_hsa_circ_260158,RMVar_hsa_circ_260159,RMVar_hsa_circ_98205,RMVar_hsa_circ_113261,RMVar_hsa_circ_76421,RMVar_hsa_circ_119813,RMVar_hsa_circ_260169,RMVar_hsa_circ_260170,RMVar_hsa_circ_260171,RMVar_hsa_circ_95266,RMVar_hsa_circ_260172,RMVar_hsa_circ_260173,RMVar_hsa_circ_260180,RMVar_hsa_circ_113549,RMVar_hsa_circ_302177,RMVar_hsa_circ_373558,RMVar_hsa_circ_260179,RMVar_hsa_circ_315907,RMVar_hsa_circ_282031,RMVar_hsa_circ_260182,RMVar_hsa_circ_260183,RMVar_hsa_circ_260184,RMVar_hsa_circ_260181 48963 RMVar_ID_48963 Human_SNP_ID_416057403 A-to-I Human chr9 + 128992286 128992286 128992286 TGTGGCATGATCTCACTGCAGCCTCCACTCCCAGGTTCATGCGATTCTCCTGTCTAAGCCTCCCA TGTGGCATGATCTCACTGCAGCCTCCACTCCCGGGTTCATGCGATTCTCCTGTCTAAGCCTCCCA A G NUP188 Ensembl:ENSG00000095319 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1466929335 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26206728 RMVar_hsa_circ_20344,RMVar_hsa_circ_264929,RMVar_hsa_circ_125507,RMVar_hsa_circ_82302,RMVar_hsa_circ_260123,RMVar_hsa_circ_117786,RMVar_hsa_circ_260124,RMVar_hsa_circ_260125,RMVar_hsa_circ_86984,RMVar_hsa_circ_260135,RMVar_hsa_circ_117645,RMVar_hsa_circ_260142,RMVar_hsa_circ_108518,RMVar_hsa_circ_127255,RMVar_hsa_circ_108464,RMVar_hsa_circ_94885,RMVar_hsa_circ_83943,RMVar_hsa_circ_91598,RMVar_hsa_circ_84257,RMVar_hsa_circ_78164,RMVar_hsa_circ_83871,RMVar_hsa_circ_88950,RMVar_hsa_circ_260145,RMVar_hsa_circ_260149,RMVar_hsa_circ_260151,RMVar_hsa_circ_260152,RMVar_hsa_circ_260150,RMVar_hsa_circ_260147,RMVar_hsa_circ_260148,RMVar_hsa_circ_260146,RMVar_hsa_circ_260144,RMVar_hsa_circ_109440,RMVar_hsa_circ_260160,RMVar_hsa_circ_99400,RMVar_hsa_circ_81218,RMVar_hsa_circ_260158,RMVar_hsa_circ_260159,RMVar_hsa_circ_98205,RMVar_hsa_circ_113261,RMVar_hsa_circ_76421,RMVar_hsa_circ_119813,RMVar_hsa_circ_260169,RMVar_hsa_circ_260170,RMVar_hsa_circ_260171,RMVar_hsa_circ_95266,RMVar_hsa_circ_260172,RMVar_hsa_circ_260173,RMVar_hsa_circ_260180,RMVar_hsa_circ_113549,RMVar_hsa_circ_302177,RMVar_hsa_circ_373558,RMVar_hsa_circ_260179,RMVar_hsa_circ_315907,RMVar_hsa_circ_282031,RMVar_hsa_circ_260182,RMVar_hsa_circ_260183,RMVar_hsa_circ_260184,RMVar_hsa_circ_260181 48964 RMVar_ID_48964 Human_SNP_ID_416062408 A-to-I Human chr9 - 129008617 129008612 129008617 GGCAGGAGAGGATGGGCGCAGCCCTGCCACTTAACTTGTTTGTTGGTGACACAGTTGTTCAGAGT GGCAGGAGAGGATGGGCGCAGCCCTGCCACTT_____GTTTGTTGGTGACACAGTTGTTCAGAGT CAAGTT C SH3GLB2 Ensembl:ENSG00000148341 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs542107239 Functional Loss DEL dbSNP153 33..37 33 - - - Human_RBP_ID_5012903,Human_RBP_ID_5124047,Human_RBP_ID_5243892,Human_RBP_ID_18197162,Human_RBP_ID_18904444,Human_RBP_ID_26565348,Human_RBP_ID_27570321 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 48965 RMVar_ID_48965 Human_SNP_ID_416062408 A-to-I Human chr9 - 129008616 129008612 129008617 GCAGGAGAGGATGGGCGCAGCCCTGCCACTTAACTTGTTTGTTGGTGACACAGTTGTTCAGAGTG GCAGGAGAGGATGGGCGCAGCCCTGCCACTT_____GTTTGTTGGTGACACAGTTGTTCAGAGTG CAAGTT C SH3GLB2 Ensembl:ENSG00000148341 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs542107239 Functional Loss DEL dbSNP153 32..36 33 - - - Human_RBP_ID_5012903,Human_RBP_ID_5124047,Human_RBP_ID_5243892,Human_RBP_ID_18197162,Human_RBP_ID_18904444,Human_RBP_ID_26565348,Human_RBP_ID_27570321 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 48966 RMVar_ID_48966 Human_SNP_ID_416062409 A-to-I Human chr9 - 129008616 129008616 129008616 GCAGGAGAGGATGGGCGCAGCCCTGCCACTTAACTTGTTTGTTGGTGACACAGTTGTTCAGAGTG GCAGGAGAGGATGGGCGCAGCCCTGCCACTTATCTTGTTTGTTGGTGACACAGTTGTTCAGAGTG T A SH3GLB2 Ensembl:ENSG00000148341 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs951138506 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5012903,Human_RBP_ID_5124047,Human_RBP_ID_5243892,Human_RBP_ID_18197162,Human_RBP_ID_18904444,Human_RBP_ID_26565348,Human_RBP_ID_27570321 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 48967 RMVar_ID_48967 Human_SNP_ID_416063383 A-to-I Human chr9 - 129011263 129011263 129011263 TTGTCTCGGGTCAGATCTCCGGAAGCGGCAGGAGCGCTGGGTCTCCTGGTCGTGGCCGGGCAGCG TTGTCTCGGGTCAGATCTCCGGAAGCGGCAGGGGCGCTGGGTCTCCTGGTCGTGGCCGGGCAGCG T C SH3GLB2 Ensembl:ENSG00000148341 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1467573332 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5633748,Human_RBP_ID_16588675,Human_RBP_ID_21995993,Human_RBP_ID_22629976 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 48968 RMVar_ID_48968 Human_SNP_ID_416072675 A-to-I Human chr9 + 129043526 129043526 129043526 CTCCTGCTTCAGCCTCTCGAAAAGCTGGGACTACAGGCACGTGCCACCATGCCTGGCTAATTTTT CTCCTGCTTCAGCCTCTCGAAAAGCTGGGACTGCAGGCACGTGCCACCATGCCTGGCTAATTTTT A G MIGA2 Ensembl:ENSG00000148343 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1298493710 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23543 48969 RMVar_ID_48969 Human_SNP_ID_416072855 A-to-I Human chr9 + 129044097 129044097 129044097 CTCACTGTAGCCTCTGCCTTCCGGTTTCAAGCAATTCTCCTGCCTGAGCCTCCCGAGTAGCTGGG CTCACTGTAGCCTCTGCCTTCCGGTTTCAAGCGATTCTCCTGCCTGAGCCTCCCGAGTAGCTGGG A G MIGA2 Ensembl:ENSG00000148343 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1311440508 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23543 48970 RMVar_ID_48970 Human_SNP_ID_416075690 A-to-I Human chr9 + 129054351 129054351 129054351 TGGCGCACACCATGTGGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGTAGGATCCCTTGAGCCCA TGGCGCACACCATGTGGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGTAGGATCCCTTGAGCCCA A G MIGA2 Ensembl:ENSG00000148343 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1319214526 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122748,RMVar_hsa_circ_260207,RMVar_hsa_circ_124146,RMVar_hsa_circ_260208 48971 RMVar_ID_48971 Human_SNP_ID_416076344 A-to-I Human chr9 + 129056911 129056911 129056911 CAAAAATTAGCCGGGTGTGGCGGTACGTGCCTATGGTCCCAAGTACTCAGGAGGGTGAGGTGGGA CAAAAATTAGCCGGGTGTGGCGGTACGTGCCTCTGGTCCCAAGTACTCAGGAGGGTGAGGTGGGA A C MIGA2 Ensembl:ENSG00000148343 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1284624017 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122748,RMVar_hsa_circ_260207,RMVar_hsa_circ_124146,RMVar_hsa_circ_260208 48972 RMVar_ID_48972 Human_SNP_ID_416076346 A-to-I Human chr9 + 129056927 129056927 129056927 GTGGCGGTACGTGCCTATGGTCCCAAGTACTCAGGAGGGTGAGGTGGGAGAATTGCTTGAACCTG GTGGCGGTACGTGCCTATGGTCCCAAGTACTCGGGAGGGTGAGGTGGGAGAATTGCTTGAACCTG A G MIGA2 Ensembl:ENSG00000148343 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs556569450 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122748,RMVar_hsa_circ_260207,RMVar_hsa_circ_124146,RMVar_hsa_circ_260208 48973 RMVar_ID_48973 Human_SNP_ID_416076596 A-to-I Human chr9 + 129058055 129058055 129058055 TTATTAAGACTTCTGGTCAACAATAGGTTATTAGTAGTTAATAACCTACTAATAACTCCCCCTAC TTATTAAGACTTCTGGTCAACAATAGGTTATTCGTAGTTAATAACCTACTAATAACTCCCCCTAC A C MIGA2 Ensembl:ENSG00000148343 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs968417065 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122748,RMVar_hsa_circ_260207,RMVar_hsa_circ_124146,RMVar_hsa_circ_260208 48974 RMVar_ID_48974 Human_SNP_ID_416076636 A-to-I Human chr9 + 129058262 129058262 129058262 CTACCAAAGATATATACAGAAGTTAGCCAGGTATGGTGATGTATGCCTGTAGTGTCCTAGCTACT CTACCAAAGATATATACAGAAGTTAGCCAGGTGTGGTGATGTATGCCTGTAGTGTCCTAGCTACT A G MIGA2 Ensembl:ENSG00000148343 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs562186038 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122748,RMVar_hsa_circ_260207,RMVar_hsa_circ_124146,RMVar_hsa_circ_260208 48975 RMVar_ID_48975 Human_SNP_ID_416076650 A-to-I Human chr9 + 129058318 129058318 129058318 CTAGCTACTAGGGAAGCAGAGACGGAAGGATCACTTGAACTCAGGAGGTTGAGATTGTGGTTAGA CTAGCTACTAGGGAAGCAGAGACGGAAGGATCCCTTGAACTCAGGAGGTTGAGATTGTGGTTAGA A C MIGA2 Ensembl:ENSG00000148343 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1011511043 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122748,RMVar_hsa_circ_260207,RMVar_hsa_circ_124146,RMVar_hsa_circ_260208 48976 RMVar_ID_48976 Human_SNP_ID_416076651 A-to-I Human chr9 + 129058318 129058318 129058318 CTAGCTACTAGGGAAGCAGAGACGGAAGGATCACTTGAACTCAGGAGGTTGAGATTGTGGTTAGA CTAGCTACTAGGGAAGCAGAGACGGAAGGATCGCTTGAACTCAGGAGGTTGAGATTGTGGTTAGA A G MIGA2 Ensembl:ENSG00000148343 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1011511043 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_122748,RMVar_hsa_circ_260207,RMVar_hsa_circ_124146,RMVar_hsa_circ_260208 48977 RMVar_ID_48977 Human_SNP_ID_416096011 A-to-I Human chr9 + 129126271 129126271 129126271 GCTGGAGTTCAATGGTACGATCTCGGCTCACCACAACCTCCGCCTCCCGGGTTCAAACGATTCTC GCTGGAGTTCAATGGTACGATCTCGGCTCACCGCAACCTCCGCCTCCCGGGTTCAAACGATTCTC A G PTPA Ensembl:ENSG00000119383 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285531095 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93454,RMVar_hsa_circ_98099,RMVar_hsa_circ_260227,RMVar_hsa_circ_260229,RMVar_hsa_circ_260228,RMVar_hsa_circ_44760,RMVar_hsa_circ_115240,RMVar_hsa_circ_33272,RMVar_hsa_circ_347910,RMVar_hsa_circ_27350 48978 RMVar_ID_48978 Human_SNP_ID_416102526 A-to-I Human chr9 + 129147490 129147490 129147490 GGGCTAGGAGGGGCCAAGCCGAAGAGCCACCCAGGCCACAGTTCCTGTGCCTGCCTTCCCCACCC GGGCTAGGAGGGGCCAAGCCGAAGAGCCACCCGGGCCACAGTTCCTGTGCCTGCCTTCCCCACCC A G PTPA Ensembl:ENSG00000119383 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs199585719 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_846904,Human_RBP_ID_5124052 Human_miRNA_ID_3088157,Human_miRNA_ID_3088158 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 48979 RMVar_ID_48979 Human_SNP_ID_416107574 A-to-I Human chr9 + 129165738 129165738 129165738 ACAATCACAGCTCACTGTAGCCTAGATCTACCAGGCTCAAGTGATCCTCCAACCTCAACCTCCCT ACAATCACAGCTCACTGTAGCCTAGATCTACCGGGCTCAAGTGATCCTCCAACCTCAACCTCCCT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1461062812 Functional Loss SNV dbSNP153 33..33 33 - - - 48980 RMVar_ID_48980 Human_SNP_ID_416107576 A-to-I Human chr9 + 129165762 129165762 129165762 GATCTACCAGGCTCAAGTGATCCTCCAACCTCAACCTCCCTAGTAGCTGGGACTATAGGTGTGCA GATCTACCAGGCTCAAGTGATCCTCCAACCTCCACCTCCCTAGTAGCTGGGACTATAGGTGTGCA A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1344141014 Functional Loss SNV dbSNP153 33..33 33 - - - 48981 RMVar_ID_48981 Human_SNP_ID_416156300 A-to-I Human chr9 + 129345533 129345533 129345533 TGAGACAGTGTCTCACTCTGTCACTCAGGCTGAAGTGTTGTGGAACCACCACAGCTCACTGCAGC TGAGACAGTGTCTCACTCTGTCACTCAGGCTGCAGTGTTGTGGAACCACCACAGCTCACTGCAGC A C LINC01503 Ensembl:ENSG00000233901 lincRNA intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1376696210 Functional Loss SNV dbSNP153 33..33 33 - - - 48982 RMVar_ID_48982 Human_SNP_ID_416196461 A-to-I Human chr9 + 129480170 129480170 129480170 TAGAGACGGGGTTTTGCCATGTTGGCCAGACTAGTCTTGAACTCCTGACCTCAAGTGACACACCC TAGAGACGGGGTTTTGCCATGTTGGCCAGACTCGTCTTGAACTCCTGACCTCAAGTGACACACCC A C LINC00963 Ensembl:ENSG00000204054 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs755166663 Functional Loss SNV dbSNP153 33..33 33 - - - 48983 RMVar_ID_48983 Human_SNP_ID_416202876 A-to-I Human chr9 + 129502851 129502851 129502851 CCTTGTGATCCACCCAAGGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGTGC CCTTGTGATCCACCCAAGGCCTCGGCCTCCCACAGTGCTGGGATTACAGGCATGAGCCACCGTGC A C LINC00963 Ensembl:ENSG00000204054 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1022256089 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27128,RMVar_hsa_circ_260238,RMVar_hsa_circ_86762 48984 RMVar_ID_48984 Human_SNP_ID_416202877 A-to-I Human chr9 + 129502851 129502851 129502851 CCTTGTGATCCACCCAAGGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGTGC CCTTGTGATCCACCCAAGGCCTCGGCCTCCCAGAGTGCTGGGATTACAGGCATGAGCCACCGTGC A G LINC00963 Ensembl:ENSG00000204054 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1022256089 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27128,RMVar_hsa_circ_260238,RMVar_hsa_circ_86762 48985 RMVar_ID_48985 Human_SNP_ID_416203236 A-to-I Human chr9 + 129504142 129504142 129504142 CAGAATTTTCCCAGTTGTAGAAAGATGGGGCCAGGTGCAGTGGCTCACGCCTGTAATCCCAGCAT CAGAATTTTCCCAGTTGTAGAAAGATGGGGCCCGGTGCAGTGGCTCACGCCTGTAATCCCAGCAT A C LINC00963 Ensembl:ENSG00000204054 lincRNA exon GSE100210;GSE99789;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,29796672,32596459 RNA-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 48986 RMVar_ID_48986 Human_SNP_ID_416203244 A-to-I Human chr9 + 129504164 129504164 129504164 AGATGGGGCCAGGTGCAGTGGCTCACGCCTGTAATCCCAGCATTTTGGGAGTACAAGGTGGGCGG AGATGGGGCCAGGTGCAGTGGCTCACGCCTGTGATCCCAGCATTTTGGGAGTACAAGGTGGGCGG A G LINC00963 Ensembl:ENSG00000204054 lincRNA exon GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line - 32596459 RNA-Seq:(High) rs11554682 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 48987 RMVar_ID_48987 Human_SNP_ID_416203326 A-to-I Human chr9 + 129504313 129504312 129504313 GGGCGTGGCGATGCATGCCTGTAATCCCAGCTACTCGGGAGGCTGAGCCAGGAGAATTGCTTGAA GGGCGTGGCGATGCATGCCTGTAATCCCAGCT_CTCGGGAGGCTGAGCCAGGAGAATTGCTTGAA TA T LINC00963 Ensembl:ENSG00000204054 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1316738105 Functional Loss DEL dbSNP153 33..33 33 - - - Human_miRNA_ID_2083268,Human_miRNA_ID_2269374,Human_miRNA_ID_3154652,Human_miRNA_ID_3165429 RMVar_hsa_circ_373652,RMVar_hsa_circ_260241 48988 RMVar_ID_48988 Human_SNP_ID_416203327 A-to-I Human chr9 + 129504313 129504313 129504313 GGGCGTGGCGATGCATGCCTGTAATCCCAGCTACTCGGGAGGCTGAGCCAGGAGAATTGCTTGAA GGGCGTGGCGATGCATGCCTGTAATCCCAGCTGCTCGGGAGGCTGAGCCAGGAGAATTGCTTGAA A G LINC00963 Ensembl:ENSG00000204054 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404648241 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2083268,Human_miRNA_ID_2269374,Human_miRNA_ID_3154652,Human_miRNA_ID_3165429 RMVar_hsa_circ_373652,RMVar_hsa_circ_260241 48989 RMVar_ID_48989 Human_SNP_ID_416203358 A-to-I Human chr9 + 129504406 129504406 129504406 AGATCGCGCCACTACACTCCAGTCCGGGCGACAGAGCAAGAGTCCATTCCCCCACCACCAAAAAA AGATCGCGCCACTACACTCCAGTCCGGGCGACGGAGCAAGAGTCCATTCCCCCACCACCAAAAAA A G LINC00963 Ensembl:ENSG00000204054 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1164327948 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_373652,RMVar_hsa_circ_260241 48990 RMVar_ID_48990 Human_SNP_ID_416203359 A-to-I Human chr9 + 129504406 129504406 129504406 AGATCGCGCCACTACACTCCAGTCCGGGCGACAGAGCAAGAGTCCATTCCCCCACCACCAAAAAA AGATCGCGCCACTACACTCCAGTCCGGGCGACTGAGCAAGAGTCCATTCCCCCACCACCAAAAAA A T LINC00963 Ensembl:ENSG00000204054 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1164327948 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_373652,RMVar_hsa_circ_260241 48991 RMVar_ID_48991 Human_SNP_ID_416203360 A-to-I Human chr9 + 129504411 129504411 129504411 GCGCCACTACACTCCAGTCCGGGCGACAGAGCAAGAGTCCATTCCCCCACCACCAAAAAAAAAAA GCGCCACTACACTCCAGTCCGGGCGACAGAGCGAGAGTCCATTCCCCCACCACCAAAAAAAAAAA A G LINC00963 Ensembl:ENSG00000204054 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1473007826 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2945539,Human_miRNA_ID_3205764 RMVar_hsa_circ_373652,RMVar_hsa_circ_260241 48992 RMVar_ID_48992 Human_SNP_ID_416203869 A-to-I Human chr9 + 129506161 129506161 129506161 CAGGGTTTCACCATGTTGCCCAGGCTGGTCTCAAACTCCTGAGCTCAGGTGATCCGCCTGCCTTG CAGGGTTTCACCATGTTGCCCAGGCTGGTCTCGAACTCCTGAGCTCAGGTGATCCGCCTGCCTTG A G LINC00963 Ensembl:ENSG00000204054 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1303096258 Functional Loss SNV dbSNP153 33..33 33 - - - 48993 RMVar_ID_48993 Human_SNP_ID_416204017 A-to-I Human chr9 + 129506558 129506558 129506558 ACGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCACGATATTGGCTCACTGCAAGCTCCGCCTCCTG ACGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCGATATTGGCTCACTGCAAGCTCCGCCTCCTG A G LINC00963 Ensembl:ENSG00000204054 lincRNA intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1383550814 Functional Loss SNV dbSNP153 33..33 33 - - - 48994 RMVar_ID_48994 Human_SNP_ID_416204025 A-to-I Human chr9 + 129506571 129506571 129506571 CAGGCTGGAGTGCAGTGGCACGATATTGGCTCACTGCAAGCTCCGCCTCCTGGGTTCACACCATT CAGGCTGGAGTGCAGTGGCACGATATTGGCTCCCTGCAAGCTCCGCCTCCTGGGTTCACACCATT A C LINC00963 Ensembl:ENSG00000204054 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1316569539 Functional Loss SNV dbSNP153 33..33 33 - - - 48995 RMVar_ID_48995 Human_SNP_ID_416204036 A-to-I Human chr9 + 129506601 129506601 129506601 TCACTGCAAGCTCCGCCTCCTGGGTTCACACCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGA TCACTGCAAGCTCCGCCTCCTGGGTTCACACCGTTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGA A G LINC00963 Ensembl:ENSG00000204054 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs940788832 Functional Loss SNV dbSNP153 33..33 33 - - - 48996 RMVar_ID_48996 Human_SNP_ID_416204058 A-to-I Human chr9 + 129506649 129506649 129506649 CTCCCGAGTAGCTGGGACTACAGGCGCCCGCCACCTCGCCCGTCTAATTTTTTGTATTTTTAGTA CTCCCGAGTAGCTGGGACTACAGGCGCCCGCCGCCTCGCCCGTCTAATTTTTTGTATTTTTAGTA A G LINC00963 Ensembl:ENSG00000204054 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1455050151 Functional Loss SNV dbSNP153 33..33 33 - - - 48997 RMVar_ID_48997 Human_SNP_ID_416204077 A-to-I Human chr9 + 129506703 129506703 129506703 TATTTTTAGTAGAGGCGGGGCTTCACCGTGTTAGCCAGGATGGTCTCAATCTCCTGACCTCGTCA TATTTTTAGTAGAGGCGGGGCTTCACCGTGTTCGCCAGGATGGTCTCAATCTCCTGACCTCGTCA A C LINC00963 Ensembl:ENSG00000204054 lincRNA intron GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,29796672,31158229,31158229 RNA-Seq:(High) rs997177743 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1089630 48998 RMVar_ID_48998 Human_SNP_ID_416204078 A-to-I Human chr9 + 129506703 129506703 129506703 TATTTTTAGTAGAGGCGGGGCTTCACCGTGTTAGCCAGGATGGTCTCAATCTCCTGACCTCGTCA TATTTTTAGTAGAGGCGGGGCTTCACCGTGTTGGCCAGGATGGTCTCAATCTCCTGACCTCGTCA A G LINC00963 Ensembl:ENSG00000204054 lincRNA intron GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,29796672,31158229,31158229 RNA-Seq:(High) rs997177743 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1089630 48999 RMVar_ID_48999 Human_SNP_ID_416204081 A-to-I Human chr9 + 129506718 129506718 129506718 CGGGGCTTCACCGTGTTAGCCAGGATGGTCTCAATCTCCTGACCTCGTCATCCGCCCGTCTCGGC CGGGGCTTCACCGTGTTAGCCAGGATGGTCTCGATCTCCTGACCTCGTCATCCGCCCGTCTCGGC A G LINC00963 Ensembl:ENSG00000204054 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs3207264 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1089552,Human_Splice_Rec_1089630 49000 RMVar_ID_49000 Human_SNP_ID_416204098 A-to-I Human chr9 + 129506776 129506776 129506776 TCTCGGCCTCCCATAGTGCTGGGATTACAGGCATGAGCCACCACGCCCGGCTGTTTTATTTCTTA TCTCGGCCTCCCATAGTGCTGGGATTACAGGCGTGAGCCACCACGCCCGGCTGTTTTATTTCTTA A G LINC00963 Ensembl:ENSG00000204054 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1010647889 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1089552,Human_Splice_Rec_1089630 49001 RMVar_ID_49001 Human_SNP_ID_416204103 A-to-I Human chr9 + 129506786 129506786 129506786 CCATAGTGCTGGGATTACAGGCATGAGCCACCACGCCCGGCTGTTTTATTTCTTATAACTGTACA CCATAGTGCTGGGATTACAGGCATGAGCCACCGCGCCCGGCTGTTTTATTTCTTATAACTGTACA A G LINC00963 Ensembl:ENSG00000204054 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs3207267 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1089552 49002 RMVar_ID_49002 Human_SNP_ID_416204282 A-to-I Human chr9 + 129507539 129507539 129507539 AGCTGGGCGTGGTGGCACACACCTGTAATCCCAGCAGCTCGGGAGGCTGAGGCAGGAGAATTGTT AGCTGGGCGTGGTGGCACACACCTGTAATCCCGGCAGCTCGGGAGGCTGAGGCAGGAGAATTGTT A G LINC00963 Ensembl:ENSG00000204054 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1344029440 Functional Loss SNV dbSNP153 33..33 33 - - - 49003 RMVar_ID_49003 Human_SNP_ID_416204437 A-to-I Human chr9 + 129508190 129508190 129508190 GAGGGGCAGAGGCAGGTGGATTACCTGAGGTCAGGAGTTTGAGACCAGCCTGGCCAACATGGCAA GAGGGGCAGAGGCAGGTGGATTACCTGAGGTCGGGAGTTTGAGACCAGCCTGGCCAACATGGCAA A G LINC00963 Ensembl:ENSG00000204054 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1269881696 Functional Loss SNV dbSNP153 33..33 33 - - - 49004 RMVar_ID_49004 Human_SNP_ID_416204458 A-to-I Human chr9 + 129508293 129508293 129508293 ATGGTGGTGCATATCTGTAGTCCCAGCTACTCAGGAGGCTGAGCAGGAGAATCACTTGAACTCAG ATGGTGGTGCATATCTGTAGTCCCAGCTACTCCGGAGGCTGAGCAGGAGAATCACTTGAACTCAG A C LINC00963 Ensembl:ENSG00000204054 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1197410670 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8697796 49005 RMVar_ID_49005 Human_SNP_ID_416204987 A-to-I Human chr9 + 129510250 129510250 129510250 TGACCTCATGATCCGCCCACTTCGTCCTCCCAAAATGCTGGGATTACAGGCATGAGCCACTGCAC TGACCTCATGATCCGCCCACTTCGTCCTCCCAGAATGCTGGGATTACAGGCATGAGCCACTGCAC A G LINC00963 Ensembl:ENSG00000204054 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs111798086 Functional Loss SNV dbSNP153 33..33 33 - - - 49006 RMVar_ID_49006 Human_SNP_ID_416205102 A-to-I Human chr9 + 129510705 129510705 129510705 ATTGCTTGAGCCCAGAAGTTCGAGAGCAGCCTAGGCAACAAGGCAAAACCTCGTCTCTACTAAAA ATTGCTTGAGCCCAGAAGTTCGAGAGCAGCCTGGGCAACAAGGCAAAACCTCGTCTCTACTAAAA A G LINC00963 Ensembl:ENSG00000204054 lincRNA intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1411553204 Functional Loss SNV dbSNP153 33..33 33 - - - 49007 RMVar_ID_49007 Human_SNP_ID_416205105 A-to-I Human chr9 + 129510712 129510712 129510712 GAGCCCAGAAGTTCGAGAGCAGCCTAGGCAACAAGGCAAAACCTCGTCTCTACTAAAAAGTAGCC GAGCCCAGAAGTTCGAGAGCAGCCTAGGCAACGAGGCAAAACCTCGTCTCTACTAAAAAGTAGCC A G LINC00963 Ensembl:ENSG00000204054 lincRNA intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1230433504 Functional Loss SNV dbSNP153 33..33 33 - - - 49008 RMVar_ID_49008 Human_SNP_ID_416205108 A-to-I Human chr9 + 129510717 129510716 129510717 CAGAAGTTCGAGAGCAGCCTAGGCAACAAGGCAAAACCTCGTCTCTACTAAAAAGTAGCCAGGCA CAGAAGTTCGAGAGCAGCCTAGGCAACAAGGC_AAACCTCGTCTCTACTAAAAAGTAGCCAGGCA CA C LINC00963 Ensembl:ENSG00000204054 lincRNA intron GSE123020:GSM3490829,GSM3490830,GSM3490831 esophageal squamous carcinoma cells,EC109 cell line - 32596459 RNA-Seq:(High) rs1298257614 Functional Loss DEL dbSNP153 33..33 33 - - - 49009 RMVar_ID_49009 Human_SNP_ID_416205129 A-to-I Human chr9 + 129510777 129510777 129510777 AGGCATGATGGTATATGCCTGTAGTCCCAGCTACTCAGGAGGCCAAGGCATGCAGATTGATTGAA AGGCATGATGGTATATGCCTGTAGTCCCAGCTGCTCAGGAGGCCAAGGCATGCAGATTGATTGAA A G LINC00963 Ensembl:ENSG00000204054 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1204759839 Functional Loss SNV dbSNP153 33..33 33 - - - 49010 RMVar_ID_49010 Human_SNP_ID_416205130 A-to-I Human chr9 + 129510781 129510779 129510781 ATGATGGTATATGCCTGTAGTCCCAGCTACTCAGGAGGCCAAGGCATGCAGATTGATTGAACCCG ATGATGGTATATGCCTGTAGTCCCAGCTACT__GGAGGCCAAGGCATGCAGATTGATTGAACCCG TCA T LINC00963 Ensembl:ENSG00000204054 lincRNA intron GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs1403556076 Functional Loss DEL dbSNP153 32..33 33 - - - 49011 RMVar_ID_49011 Human_SNP_ID_416205132 A-to-I Human chr9 + 129510789 129510789 129510789 ATATGCCTGTAGTCCCAGCTACTCAGGAGGCCAAGGCATGCAGATTGATTGAACCCGGAAGGTGG ATATGCCTGTAGTCCCAGCTACTCAGGAGGCCGAGGCATGCAGATTGATTGAACCCGGAAGGTGG A G LINC00963 Ensembl:ENSG00000204054 lincRNA intron GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs1321098359 Functional Loss SNV dbSNP153 33..33 33 - - - 49012 RMVar_ID_49012 Human_SNP_ID_416205142 A-to-I Human chr9 + 129510815 129510814 129510815 GAGGCCAAGGCATGCAGATTGATTGAACCCGGAAGGTGGAGGCTACAGTGAATTGTGATCTCGCC GAGGCCAAGGCATGCAGATTGATTGAACCCGG_AGGTGGAGGCTACAGTGAATTGTGATCTCGCC GA G LINC00963 Ensembl:ENSG00000204054 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs34361685 Functional Loss DEL dbSNP153 33..33 33 - - - 49013 RMVar_ID_49013 Human_SNP_ID_416224026 A-to-I Human chr9 + 129582719 129582719 129582719 GCAATCTCGGCTCACTGCAGTCACCTCCTCTCAGGTTCAAGTGATTCTCCTGCCTCTGCCTCCTG GCAATCTCGGCTCACTGCAGTCACCTCCTCTCGGGTTCAAGTGATTCTCCTGCCTCTGCCTCCTG A G AL391056.1 Ensembl:ENSG00000227619 lincRNA exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs953215691 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1089738,Human_Splice_Rec_1089744,Human_Splice_Rec_1089750,Human_Splice_Rec_1089751,Human_Splice_Rec_1089760,Human_Splice_Rec_1089766,Human_Splice_Rec_1089774 49014 RMVar_ID_49014 Human_SNP_ID_416286509 A-to-I Human chr9 + 129808378 129808378 129808378 AAATTAGAAGGGGCGTCGTGGCAGGCGCCTGTAATCCCAGCTACTCAGGAGGTTGAGGCAGAAGA AAATTAGAAGGGGCGTCGTGGCAGGCGCCTGTGATCCCAGCTACTCAGGAGGTTGAGGCAGAAGA A G TOR1B Ensembl:ENSG00000136816 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs947545527 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98530,RMVar_hsa_circ_109271,RMVar_hsa_circ_260248,RMVar_hsa_circ_260249,RMVar_hsa_circ_314055,RMVar_hsa_circ_260251 49015 RMVar_ID_49015 Human_SNP_ID_416286523 A-to-I Human chr9 + 129808451 129808451 129808451 AACCCGGAAGGTGGAGGTTGCAGTGAGCTGATATTGCGCCACTGCACTCCAGCCTGCGTGACAGA AACCCGGAAGGTGGAGGTTGCAGTGAGCTGATGTTGCGCCACTGCACTCCAGCCTGCGTGACAGA A G TOR1B Ensembl:ENSG00000136816 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1408366922 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98530,RMVar_hsa_circ_109271,RMVar_hsa_circ_260248,RMVar_hsa_circ_260249,RMVar_hsa_circ_314055,RMVar_hsa_circ_260251 49016 RMVar_ID_49016 Human_SNP_ID_416286625 A-to-I Human chr9 + 129808717 129808717 129808717 GATTACAGGCATGCACCACCATTAGCCTGGCTAATTTTTGTGTTTTTAGTAGAGATGGGGTTACT GATTACAGGCATGCACCACCATTAGCCTGGCTCATTTTTGTGTTTTTAGTAGAGATGGGGTTACT A C TOR1B Ensembl:ENSG00000136816 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs947698165 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98530,RMVar_hsa_circ_109271,RMVar_hsa_circ_260248,RMVar_hsa_circ_260249,RMVar_hsa_circ_314055,RMVar_hsa_circ_260251 49017 RMVar_ID_49017 Human_SNP_ID_416286626 A-to-I Human chr9 + 129808717 129808717 129808717 GATTACAGGCATGCACCACCATTAGCCTGGCTAATTTTTGTGTTTTTAGTAGAGATGGGGTTACT GATTACAGGCATGCACCACCATTAGCCTGGCTGATTTTTGTGTTTTTAGTAGAGATGGGGTTACT A G TOR1B Ensembl:ENSG00000136816 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs947698165 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98530,RMVar_hsa_circ_109271,RMVar_hsa_circ_260248,RMVar_hsa_circ_260249,RMVar_hsa_circ_314055,RMVar_hsa_circ_260251 49018 RMVar_ID_49018 Human_SNP_ID_416286631 A-to-I Human chr9 + 129808747 129808747 129808747 CTAATTTTTGTGTTTTTAGTAGAGATGGGGTTACTCTATGTTGGTCAGGCTGGCCTTGAACTCCC CTAATTTTTGTGTTTTTAGTAGAGATGGGGTTGCTCTATGTTGGTCAGGCTGGCCTTGAACTCCC A G TOR1B Ensembl:ENSG00000136816 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1260837376 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98530,RMVar_hsa_circ_109271,RMVar_hsa_circ_260248,RMVar_hsa_circ_260249,RMVar_hsa_circ_314055,RMVar_hsa_circ_260251 49019 RMVar_ID_49019 Human_SNP_ID_416286653 A-to-I Human chr9 + 129808832 129808832 129808832 CCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCACACCCAGCAGACACAGAAGTCT CCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCACACCCAGCAGACACAGAAGTCT A G TOR1B Ensembl:ENSG00000136816 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1466038114 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98530,RMVar_hsa_circ_109271,RMVar_hsa_circ_260248,RMVar_hsa_circ_260249,RMVar_hsa_circ_314055,RMVar_hsa_circ_260251 49020 RMVar_ID_49020 Human_SNP_ID_416286848 A-to-I Human chr9 + 129809392 129809392 129809392 GACTGATCGACAAAAACCTCATTGATTACTTTATCCCCTTCCTGCCTTTGGAGTACAGACATGTG GACTGATCGACAAAAACCTCATTGATTACTTTGTCCCCTTCCTGCCTTTGGAGTACAGACATGTG A G TOR1B Ensembl:ENSG00000136816 Protein coding CDS GSE56152 embryonic stem cells,wild type - 25708366 RNA-Seq:(High) rs201495837 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8157521,Human_RBP_ID_8925850,Human_RBP_ID_9314428,Human_RBP_ID_22776573,Human_RBP_ID_27131461 Human_Splice_Rec_1089910 Human_miRNA_ID_870611,Human_miRNA_ID_2063113,Human_miRNA_ID_2384507,Human_miRNA_ID_2900779 RMVar_hsa_circ_98530,RMVar_hsa_circ_109271,RMVar_hsa_circ_260248,RMVar_hsa_circ_260249,RMVar_hsa_circ_115176,RMVar_hsa_circ_260252 49021 RMVar_ID_49021 Human_SNP_ID_416289754 A-to-I Human chr9 - 129819639 129819639 129819639 ATTCTACCTCAGCCTCCTGAGTAGCTGGGACTATAAGCACCTGCCACCATACCCAGCTAATTTTT ATTCTACCTCAGCCTCCTGAGTAGCTGGGACTGTAAGCACCTGCCACCATACCCAGCTAATTTTT T C TOR1A Ensembl:ENSG00000136827 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1029388465 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119741,RMVar_hsa_circ_77463,RMVar_hsa_circ_260253,RMVar_hsa_circ_260254 49022 RMVar_ID_49022 Human_SNP_ID_416290070 A-to-I Human chr9 - 129820825 129820825 129820825 GGAAGCCAAAACCGGCTGATCCCTTGAGCTCAAGAGTTCCAGACCAGCCTGGGGAACATGGTGAA GGAAGCCAAAACCGGCTGATCCCTTGAGCTCAGGAGTTCCAGACCAGCCTGGGGAACATGGTGAA T C TOR1A Ensembl:ENSG00000136827 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs891974851 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119741,RMVar_hsa_circ_77463,RMVar_hsa_circ_260253,RMVar_hsa_circ_260254 49023 RMVar_ID_49023 Human_SNP_ID_416290273 A-to-I Human chr9 - 129821643 129821643 129821643 GTGATCTGCCTACCTCAGCCTCCCAGAGTGCTAGGATTACAGGCGTGAGCCACCTTGCCCAGCCG GTGATCTGCCTACCTCAGCCTCCCAGAGTGCTGGGATTACAGGCGTGAGCCACCTTGCCCAGCCG T C TOR1A Ensembl:ENSG00000136827 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1244590442 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119741,RMVar_hsa_circ_77463,RMVar_hsa_circ_260253,RMVar_hsa_circ_260254 49024 RMVar_ID_49024 Human_SNP_ID_416292126 A-to-I Human chr9 - 129827951 129827951 129827951 CAGTCTCTACTGAAAATACAGAAAAGTTAGCCAGGCGTGGTGGCACATGCCTGTAATCCCAGCTG CAGTCTCTACTGAAAATACAGAAAAGTTAGCCGGGCGTGGTGGCACATGCCTGTAATCCCAGCTG T C C9orf78 Ensembl:ENSG00000136819 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1275348728 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8224686 49025 RMVar_ID_49025 Human_SNP_ID_416297420 A-to-I Human chr9 + 129846395 129846395 129846395 CTCCCATCACAGCTTCCCGAGTAGCTGGGACTACAGGTGCGTGCACCACCATGCCCACCTAATTT CTCCCATCACAGCTTCCCGAGTAGCTGGGACTGCAGGTGCGTGCACCACCATGCCCACCTAATTT A G USP20 Ensembl:ENSG00000136878 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1478590955 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126230,RMVar_hsa_circ_260259 49026 RMVar_ID_49026 Human_SNP_ID_416300900 A-to-I Human chr9 + 129859474 129859474 129859474 TTTCATATTTTTAGTAGAGTCAGGGTTTTGCCATGTTGACTAGGCTGGTCTTGAACTCCTGACCT TTTCATATTTTTAGTAGAGTCAGGGTTTTGCCCTGTTGACTAGGCTGGTCTTGAACTCCTGACCT A C USP20 Ensembl:ENSG00000136878 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1003997284 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78703,RMVar_hsa_circ_38807,RMVar_hsa_circ_126230,RMVar_hsa_circ_281482,RMVar_hsa_circ_260259,RMVar_hsa_circ_113952,RMVar_hsa_circ_260260,RMVar_hsa_circ_331693,RMVar_hsa_circ_346732,RMVar_hsa_circ_121017,RMVar_hsa_circ_260261,RMVar_hsa_circ_260262,RMVar_hsa_circ_97867,RMVar_hsa_circ_260263,RMVar_hsa_circ_260264,RMVar_hsa_circ_260265 49027 RMVar_ID_49027 Human_SNP_ID_416312392 A-to-I Human chr9 - 129899350 129899350 129899350 GATCTGGCCGGGCATGGTGGCTCACACCTGTAATCCTAGAACTTTGGGAGGCTGAGGCGGGCAGG GATCTGGCCGGGCATGGTGGCTCACACCTGTAGTCCTAGAACTTTGGGAGGCTGAGGCGGGCAGG T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1233613724 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82132,RMVar_hsa_circ_105844,RMVar_hsa_circ_116881,RMVar_hsa_circ_260268,RMVar_hsa_circ_260269,RMVar_hsa_circ_289358,RMVar_hsa_circ_363513,RMVar_hsa_circ_260270,RMVar_hsa_circ_260272,RMVar_hsa_circ_69780,RMVar_hsa_circ_260271 49028 RMVar_ID_49028 Human_SNP_ID_416312462 A-to-I Human chr9 - 129899667 129899667 129899667 TAGAGTGCAGTGGTGCAATCATGGCTCACTGCAGCCTTGACCTCCTGGGCTCAAGTGATCCTCCA TAGAGTGCAGTGGTGCAATCATGGCTCACTGCGGCCTTGACCTCCTGGGCTCAAGTGATCCTCCA T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1392145374 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82132,RMVar_hsa_circ_105844,RMVar_hsa_circ_116881,RMVar_hsa_circ_260268,RMVar_hsa_circ_260269,RMVar_hsa_circ_289358,RMVar_hsa_circ_363513,RMVar_hsa_circ_260270,RMVar_hsa_circ_260272,RMVar_hsa_circ_69780,RMVar_hsa_circ_260271 49029 RMVar_ID_49029 Human_SNP_ID_416313566 A-to-I Human chr9 - 129903928 129903928 129903928 GGTTCAAGTGATTCTCCTGCCTAAGCCTCCCAAGTAGCTGGGATTAAGGGGACATGCCATCACGC GGTTCAAGTGATTCTCCTGCCTAAGCCTCCCATGTAGCTGGGATTAAGGGGACATGCCATCACGC T A FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs866953149 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82132,RMVar_hsa_circ_116881,RMVar_hsa_circ_260269,RMVar_hsa_circ_289358,RMVar_hsa_circ_363513,RMVar_hsa_circ_260272,RMVar_hsa_circ_69780,RMVar_hsa_circ_260271,RMVar_hsa_circ_378645,RMVar_hsa_circ_283678,RMVar_hsa_circ_260274,RMVar_hsa_circ_74258,RMVar_hsa_circ_260275,RMVar_hsa_circ_114146,RMVar_hsa_circ_289649,RMVar_hsa_circ_333687,RMVar_hsa_circ_260276,RMVar_hsa_circ_260277 49030 RMVar_ID_49030 Human_SNP_ID_416313567 A-to-I Human chr9 - 129903928 129903928 129903928 GGTTCAAGTGATTCTCCTGCCTAAGCCTCCCAAGTAGCTGGGATTAAGGGGACATGCCATCACGC GGTTCAAGTGATTCTCCTGCCTAAGCCTCCCAGGTAGCTGGGATTAAGGGGACATGCCATCACGC T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs866953149 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82132,RMVar_hsa_circ_116881,RMVar_hsa_circ_260269,RMVar_hsa_circ_289358,RMVar_hsa_circ_363513,RMVar_hsa_circ_260272,RMVar_hsa_circ_69780,RMVar_hsa_circ_260271,RMVar_hsa_circ_378645,RMVar_hsa_circ_283678,RMVar_hsa_circ_260274,RMVar_hsa_circ_74258,RMVar_hsa_circ_260275,RMVar_hsa_circ_114146,RMVar_hsa_circ_289649,RMVar_hsa_circ_333687,RMVar_hsa_circ_260276,RMVar_hsa_circ_260277 49031 RMVar_ID_49031 Human_SNP_ID_416315651 A-to-I Human chr9 - 129911104 129911104 129911104 TAATCCCAGGACGTTGGGAGGCCGAGGTGGGCAGATCGCCTGAGGTCGGGAGTTCGAGACCAGCC TAATCCCAGGACGTTGGGAGGCCGAGGTGGGCGGATCGCCTGAGGTCGGGAGTTCGAGACCAGCC T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs375191772 Functional Loss SNV dbSNP153 33..33 33 - - - 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_260279,RMVar_hsa_circ_260280,RMVar_hsa_circ_260278 49032 RMVar_ID_49032 Human_SNP_ID_416315664 A-to-I Human chr9 - 129911153 129911153 129911153 TTTTAACAAAAGACTGTAGCAAGAGGCCGCGCATGGTGGCTCATTCCTGTAATCCCAGGACGTTG TTTTAACAAAAGACTGTAGCAAGAGGCCGCGCGTGGTGGCTCATTCCTGTAATCCCAGGACGTTG T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs867897905 Functional Loss SNV dbSNP153 33..33 33 - - - 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_260279,RMVar_hsa_circ_260280,RMVar_hsa_circ_260278 49033 RMVar_ID_49033 Human_SNP_ID_416315685 A-to-I Human chr9 - 129911247 129911247 129911247 CCACAATCAGAATCCTGCCTTGGGCAGGTGAAAGAAGGGCACGTGGAGGTCAGATAGAGAGATTC CCACAATCAGAATCCTGCCTTGGGCAGGTGAAGGAAGGGCACGTGGAGGTCAGATAGAGAGATTC T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1235038442 Functional Loss SNV dbSNP153 33..33 33 - - - 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_260279,RMVar_hsa_circ_260280,RMVar_hsa_circ_260278 49034 RMVar_ID_49034 Human_SNP_ID_416316053 A-to-I Human chr9 - 129912647 129912647 129912647 TTACTCATGTTGTCCAGGCTGGAGTGCGCAGTAGCGCAATCTCAGCTCACCACAACCTCCACCTC TTACTCATGTTGTCCAGGCTGGAGTGCGCAGTTGCGCAATCTCAGCTCACCACAACCTCCACCTC T A FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7025726 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26207083 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_260279,RMVar_hsa_circ_260280,RMVar_hsa_circ_260278 49035 RMVar_ID_49035 Human_SNP_ID_416316054 A-to-I Human chr9 - 129912647 129912647 129912647 TTACTCATGTTGTCCAGGCTGGAGTGCGCAGTAGCGCAATCTCAGCTCACCACAACCTCCACCTC TTACTCATGTTGTCCAGGCTGGAGTGCGCAGTGGCGCAATCTCAGCTCACCACAACCTCCACCTC T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7025726 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26207083 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_260279,RMVar_hsa_circ_260280,RMVar_hsa_circ_260278 49036 RMVar_ID_49036 Human_SNP_ID_416316202 A-to-I Human chr9 - 129913164 129913164 129913164 TCGCTCTGTCACTGAGGATGGAGTGCAGTGGCATGATCCTGGCTCACTGCATCCTCCGCCTCCCG TCGCTCTGTCACTGAGGATGGAGTGCAGTGGCGTGATCCTGGCTCACTGCATCCTCCGCCTCCCG T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1042450210 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7902121,Human_RBP_ID_16590265,Human_RBP_ID_23200392 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_260279,RMVar_hsa_circ_260280,RMVar_hsa_circ_260278 49037 RMVar_ID_49037 Human_SNP_ID_416316224 A-to-I Human chr9 - 129913236 129913236 129913236 GTCCAGTGTGGTAGCCACTACCATATGTAGCTATTGAGTTTTTTGTTTTTGTTTTTGTTTTGAGA GTCCAGTGTGGTAGCCACTACCATATGTAGCTGTTGAGTTTTTTGTTTTTGTTTTTGTTTTGAGA T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7029572 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_5925,GWAS_ID_5926,GWAS_ID_5927,GWAS_ID_5928,GWAS_ID_5929,GWAS_ID_5930,GWAS_ID_5931,GWAS_ID_5932,GWAS_ID_5933,GWAS_ID_5934,GWAS_ID_5935,GWAS_ID_5936,GWAS_ID_5937,GWAS_ID_5938,GWAS_ID_5939,GWAS_ID_5940,GWAS_ID_5941,GWAS_ID_5942,GWAS_ID_5943,GWAS_ID_5944,GWAS_ID_5945,GWAS_ID_5946,GWAS_ID_5947,GWAS_ID_5948,GWAS_ID_5949,GWAS_ID_5950,GWAS_ID_5951,GWAS_ID_5952,GWAS_ID_5953,GWAS_ID_5954,GWAS_ID_5955,GWAS_ID_5956,GWAS_ID_5957,GWAS_ID_5958,GWAS_ID_5959,GWAS_ID_5960,GWAS_ID_5961,GWAS_ID_5962,GWAS_ID_5963,GWAS_ID_5964,GWAS_ID_5965,GWAS_ID_5966,GWAS_ID_5967,GWAS_ID_5968,GWAS_ID_5969,GWAS_ID_5970,GWAS_ID_5971,GWAS_ID_5972,GWAS_ID_5973,GWAS_ID_5974,GWAS_ID_5975,GWAS_ID_5976,GWAS_ID_5977,GWAS_ID_5978,GWAS_ID_5979,GWAS_ID_5980,GWAS_ID_5981,GWAS_ID_5982,GWAS_ID_5983,GWAS_ID_5984,GWAS_ID_5985,GWAS_ID_5986,GWAS_ID_5987,GWAS_ID_5988,GWAS_ID_5989,GWAS_ID_5990,GWAS_ID_5991,GWAS_ID_5992,GWAS_ID_5993,GWAS_ID_5994,GWAS_ID_5995,GWAS_ID_5996,GWAS_ID_5997,GWAS_ID_5998,GWAS_ID_5999,GWAS_ID_6000,GWAS_ID_6001,GWAS_ID_6002,GWAS_ID_6003,GWAS_ID_6004 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_260279,RMVar_hsa_circ_260280,RMVar_hsa_circ_260278 49038 RMVar_ID_49038 Human_SNP_ID_416316453 A-to-I Human chr9 - 129914128 129914128 129914128 TGTGGGACCAGGTGTGGTGGCTCACGCCTGTAATCTCTGCACTTTGGGAGGTGGGGGCAGGCAGA TGTGGGACCAGGTGTGGTGGCTCACGCCTGTACTCTCTGCACTTTGGGAGGTGGGGGCAGGCAGA T G FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1241979361 Functional Loss SNV dbSNP153 33..33 33 - - - 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_260279,RMVar_hsa_circ_260280,RMVar_hsa_circ_260278 49039 RMVar_ID_49039 Human_SNP_ID_416316497 A-to-I Human chr9 - 129914284 129914284 129914284 CCTGGAATCCCAGTGCTTTGGAAGGCTGAGGCAGGAAGATTGCCTGAGCCCAGGAGCTCAAGGTT CCTGGAATCCCAGTGCTTTGGAAGGCTGAGGCGGGAAGATTGCCTGAGCCCAGGAGCTCAAGGTT T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,cerebellum - 29129909,30559470 RNA-Seq:(High) rs550582239 Functional Loss SNV dbSNP153 33..33 33 - - - 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_260279,RMVar_hsa_circ_260280,RMVar_hsa_circ_260278 49040 RMVar_ID_49040 Human_SNP_ID_416316853 A-to-I Human chr9 - 129915441 129915441 129915441 AGAACTGCTTGAACCCGGGAGGTGAAGGGTGCAGTGAGCCGAGATTATACCACTGGACTTCCAGC AGAACTGCTTGAACCCGGGAGGTGAAGGGTGCGGTGAGCCGAGATTATACCACTGGACTTCCAGC T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs537239582 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1119500,Human_RBP_ID_18140680,Human_RBP_ID_26207101 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_260279,RMVar_hsa_circ_260280,RMVar_hsa_circ_260278 49041 RMVar_ID_49041 Human_SNP_ID_416316854 A-to-I Human chr9 - 129915441 129915441 129915441 AGAACTGCTTGAACCCGGGAGGTGAAGGGTGCAGTGAGCCGAGATTATACCACTGGACTTCCAGC AGAACTGCTTGAACCCGGGAGGTGAAGGGTGCCGTGAGCCGAGATTATACCACTGGACTTCCAGC T G FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs537239582 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1119500,Human_RBP_ID_18140680,Human_RBP_ID_26207101 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_260279,RMVar_hsa_circ_260280,RMVar_hsa_circ_260278 49042 RMVar_ID_49042 Human_SNP_ID_416317116 A-to-I Human chr9 - 129916461 129916461 129916461 AGGTGTGCACCACCACACCCGGCTAATACTGTATTTTTAGTAGAGACAGGGTTTCTCCGTGTTGG AGGTGTGCACCACCACACCCGGCTAATACTGTGTTTTTAGTAGAGACAGGGTTTCTCCGTGTTGG T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1564319340 Functional Loss SNV dbSNP153 33..33 33 - - - 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_260279,RMVar_hsa_circ_260280,RMVar_hsa_circ_260278 49043 RMVar_ID_49043 Human_SNP_ID_416317291 A-to-I Human chr9 - 129917150 129917150 129917150 ACATTAGCTGGGCGTGGTGGCAGGCACCTGTAATCCCAGCTACTCAGGAGGCTGAAGCAGGAAAA ACATTAGCTGGGCGTGGTGGCAGGCACCTGTAGTCCCAGCTACTCAGGAGGCTGAAGCAGGAAAA T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1404812517 Functional Loss SNV dbSNP153 33..33 33 - - - 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_260279,RMVar_hsa_circ_260280,RMVar_hsa_circ_260278 49044 RMVar_ID_49044 Human_SNP_ID_416317314 A-to-I Human chr9 - 129917214 129917213 129917214 AGGTCAGGAGTTCAAGACCAGCCTGACCAACAAGGCGAAACCCCGTCTCTACTAAAAATACAAAA AGGTCAGGAGTTCAAGACCAGCCTGACCAACA_GGCGAAACCCCGTCTCTACTAAAAATACAAAA CT C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1314354761 Functional Loss DEL dbSNP153 33..33 33 - - - 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_260279,RMVar_hsa_circ_260280,RMVar_hsa_circ_260278 49045 RMVar_ID_49045 Human_SNP_ID_416317316 A-to-I Human chr9 - 129917217 129917217 129917217 ACGAGGTCAGGAGTTCAAGACCAGCCTGACCAACAAGGCGAAACCCCGTCTCTACTAAAAATACA ACGAGGTCAGGAGTTCAAGACCAGCCTGACCATCAAGGCGAAACCCCGTCTCTACTAAAAATACA T A FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1359070482 Functional Loss SNV dbSNP153 33..33 33 - - - 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_260279,RMVar_hsa_circ_260280,RMVar_hsa_circ_260278 49046 RMVar_ID_49046 Human_SNP_ID_416317320 A-to-I Human chr9 - 129917241 129917241 129917241 AGCACTTTGGGAGGCGGGCGGATCACGAGGTCAGGAGTTCAAGACCAGCCTGACCAACAAGGCGA AGCACTTTGGGAGGCGGGCGGATCACGAGGTCGGGAGTTCAAGACCAGCCTGACCAACAAGGCGA T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs949114281 Functional Loss SNV dbSNP153 33..33 33 - - - 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_260279,RMVar_hsa_circ_260280,RMVar_hsa_circ_260278 49047 RMVar_ID_49047 Human_SNP_ID_416317362 A-to-I Human chr9 - 129917430 129917430 129917430 TACTCAGGAGGCTGAGGTGCGAGGATCATTTGAGCTCTAGAGGTTGAGGCTTCAGTGAGCTGGGA TACTCAGGAGGCTGAGGTGCGAGGATCATTTGCGCTCTAGAGGTTGAGGCTTCAGTGAGCTGGGA T G FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs564996331 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16590286 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_260279,RMVar_hsa_circ_260280,RMVar_hsa_circ_260278 49048 RMVar_ID_49048 Human_SNP_ID_416318254 A-to-I Human chr9 - 129921470 129921469 129921470 AGAATCGCTTGGACCTGGGAAGTGGAGGTTGCAGTGAGCCAAGATCACGCTATTGCACTCCAGCC AGAATCGCTTGGACCTGGGAAGTGGAGGTTGC_GTGAGCCAAGATCACGCTATTGCACTCCAGCC CT C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1390858714 Functional Loss DEL dbSNP153 33..33 33 - - - 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_260279,RMVar_hsa_circ_260280,RMVar_hsa_circ_260278 49049 RMVar_ID_49049 Human_SNP_ID_416318260 A-to-I Human chr9 - 129921499 129921499 129921499 ATCCCAGCTACTCGGGAAACTGAGGCAGGAGAATCGCTTGGACCTGGGAAGTGGAGGTTGCAGTG ATCCCAGCTACTCGGGAAACTGAGGCAGGAGACTCGCTTGGACCTGGGAAGTGGAGGTTGCAGTG T G FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs150628547 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8697908 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_260279,RMVar_hsa_circ_260280,RMVar_hsa_circ_260278 49050 RMVar_ID_49050 Human_SNP_ID_416318582 A-to-I Human chr9 - 129923122 129923122 129923122 GTGATAGTTCACATCTGTAATCCTAGCACTTTAGGAGGCCAAGGCAGGAGGATTGCTTGAGCTCA GTGATAGTTCACATCTGTAATCCTAGCACTTTGGGAGGCCAAGGCAGGAGGATTGCTTGAGCTCA T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233;GSE107867 cultured B-cells;ASD brains,temporal_cortex - 24183664,30559470 RNA-Seq:(High) rs1269809169 Functional Loss SNV dbSNP153 33..33 33 - - - 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_260279,RMVar_hsa_circ_260280,RMVar_hsa_circ_260278 49051 RMVar_ID_49051 Human_SNP_ID_416318592 A-to-I Human chr9 - 129923149 129923149 129923149 TCTAAAACTAGCGACCTGAGACTGGGCGTGATAGTTCACATCTGTAATCCTAGCACTTTAGGAGG TCTAAAACTAGCGACCTGAGACTGGGCGTGATGGTTCACATCTGTAATCCTAGCACTTTAGGAGG T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs554024933 Functional Loss SNV dbSNP153 33..33 33 - - - 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_260279,RMVar_hsa_circ_260280,RMVar_hsa_circ_260278 49052 RMVar_ID_49052 Human_SNP_ID_416318640 A-to-I Human chr9 - 129923324 129923324 129923324 CGCCCGCCTCGGCCTTACAAAGTGCTGGGATTACAGGTGTGAGCCACTGCGCCCGGCCTTTTTCT CGCCCGCCTCGGCCTTACAAAGTGCTGGGATTGCAGGTGTGAGCCACTGCGCCCGGCCTTTTTCT T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1036125526 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26207144 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_260279,RMVar_hsa_circ_260280,RMVar_hsa_circ_260278 49053 RMVar_ID_49053 Human_SNP_ID_416318700 A-to-I Human chr9 - 129923541 129923541 129923541 CAGAGTCTCGCTCTGTCACCAGGCTGGAGTGCAGTGGCGTGATCTCGGCTCCCTGCAACCTCCAC CAGAGTCTCGCTCTGTCACCAGGCTGGAGTGCGGTGGCGTGATCTCGGCTCCCTGCAACCTCCAC T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1427767148 Functional Loss SNV dbSNP153 33..33 33 - - - 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_260279,RMVar_hsa_circ_260280,RMVar_hsa_circ_260278 49054 RMVar_ID_49054 Human_SNP_ID_416318731 A-to-I Human chr9 - 129923624 129923624 129923624 AGCATGGTGGTTGGAAGAAAGGAGAAAACCAGACAGCCCAGAGTTCTTTCTATTTGTTTCTTTCT AGCATGGTGGTTGGAAGAAAGGAGAAAACCAGGCAGCCCAGAGTTCTTTCTATTTGTTTCTTTCT T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1923663 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9233449 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_260279,RMVar_hsa_circ_260280,RMVar_hsa_circ_260278 49055 RMVar_ID_49055 Human_SNP_ID_416319781 A-to-I Human chr9 - 129927505 129927505 129927505 CAGCCTAACATGTCTAGCAATTTATAAAATAAATGTACAGCTGGGTAATATGGAGGCTCCGTGTA CAGCCTAACATGTCTAGCAATTTATAAAATAAGTGTACAGCTGGGTAATATGGAGGCTCCGTGTA T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4837430 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_6005,GWAS_ID_6006,GWAS_ID_6007,GWAS_ID_6008,GWAS_ID_6009,GWAS_ID_6010,GWAS_ID_6011,GWAS_ID_6012,GWAS_ID_6013,GWAS_ID_6014,GWAS_ID_6015,GWAS_ID_6016,GWAS_ID_6017,GWAS_ID_6018,GWAS_ID_6019,GWAS_ID_6020,GWAS_ID_6021,GWAS_ID_6022,GWAS_ID_6023,GWAS_ID_6024,GWAS_ID_6025,GWAS_ID_6026,GWAS_ID_6027,GWAS_ID_6028,GWAS_ID_6029,GWAS_ID_6030,GWAS_ID_6031,GWAS_ID_6032,GWAS_ID_6033,GWAS_ID_6034,GWAS_ID_6035,GWAS_ID_6036,GWAS_ID_6037,GWAS_ID_6038,GWAS_ID_6039,GWAS_ID_6040,GWAS_ID_6041,GWAS_ID_6042,GWAS_ID_6043,GWAS_ID_6044,GWAS_ID_6045,GWAS_ID_6046,GWAS_ID_6047,GWAS_ID_6048,GWAS_ID_6049,GWAS_ID_6050,GWAS_ID_6051,GWAS_ID_6052,GWAS_ID_6053,GWAS_ID_6054,GWAS_ID_6055,GWAS_ID_6056,GWAS_ID_6057,GWAS_ID_6058,GWAS_ID_6059,GWAS_ID_6060,GWAS_ID_6061,GWAS_ID_6062,GWAS_ID_6063,GWAS_ID_6064,GWAS_ID_6065,GWAS_ID_6066,GWAS_ID_6067,GWAS_ID_6068,GWAS_ID_6069,GWAS_ID_6070,GWAS_ID_6071,GWAS_ID_6072,GWAS_ID_6073,GWAS_ID_6074,GWAS_ID_6075,GWAS_ID_6076,GWAS_ID_6077,GWAS_ID_6078 RMVar_hsa_circ_82132,RMVar_hsa_circ_116881,RMVar_hsa_circ_260269,RMVar_hsa_circ_363513,RMVar_hsa_circ_260272,RMVar_hsa_circ_69780,RMVar_hsa_circ_378645,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_260279,RMVar_hsa_circ_260278,RMVar_hsa_circ_271812,RMVar_hsa_circ_359498,RMVar_hsa_circ_46271,RMVar_hsa_circ_55216,RMVar_hsa_circ_260282,RMVar_hsa_circ_369227,RMVar_hsa_circ_275039,RMVar_hsa_circ_260283,RMVar_hsa_circ_30836 49056 RMVar_ID_49056 Human_SNP_ID_416320209 A-to-I Human chr9 - 129929247 129929246 129929247 TACCACTGGGCCCGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTTGCCATGTTGGCCAGGC TACCACTGGGCCCGGCTAATTTTTGTATTTTT_GTAGAGACGGGGTTTTGCCATGTTGGCCAGGC CT C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs747099946 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_82132,RMVar_hsa_circ_116881,RMVar_hsa_circ_260269,RMVar_hsa_circ_363513,RMVar_hsa_circ_260272,RMVar_hsa_circ_69780,RMVar_hsa_circ_378645,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_260279,RMVar_hsa_circ_260278,RMVar_hsa_circ_271812,RMVar_hsa_circ_359498,RMVar_hsa_circ_46271,RMVar_hsa_circ_55216,RMVar_hsa_circ_260282,RMVar_hsa_circ_369227,RMVar_hsa_circ_275039,RMVar_hsa_circ_260283,RMVar_hsa_circ_30836 49057 RMVar_ID_49057 Human_SNP_ID_416320663 A-to-I Human chr9 - 129931133 129931133 129931133 TACCACCATGCCCAGCTAATTTTTGTAGAGAGAGGGGTCTCACCATGTTGCCCAGGCTGGTCTCA TACCACCATGCCCAGCTAATTTTTGTAGAGAGCGGGGTCTCACCATGTTGCCCAGGCTGGTCTCA T G FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1297480381 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 49058 RMVar_ID_49058 Human_SNP_ID_416320682 A-to-I Human chr9 - 129931209 129931209 129931209 TCACTGCAGCCTCAGCCTCCCAGGCTCAAGCAATCCTCCTGCCTCAGCCTCCTGAGTAACTGGAA TCACTGCAGCCTCAGCCTCCCAGGCTCAAGCAGTCCTCCTGCCTCAGCCTCCTGAGTAACTGGAA T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1259323771 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 49059 RMVar_ID_49059 Human_SNP_ID_416320856 A-to-I Human chr9 - 129931746 129931746 129931746 TTACCCAGGCTGGAGTGCAGTGGCGCAGTCACAGCTTACTGTATACTTGACCTCCTGAGCTCAAG TTACCCAGGCTGGAGTGCAGTGGCGCAGTCACGGCTTACTGTATACTTGACCTCCTGAGCTCAAG T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs980802848 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 49060 RMVar_ID_49060 Human_SNP_ID_416321542 A-to-I Human chr9 - 129934863 129934851 129934863 ATTACCAAGAAGTGGGCTGGGCGTGGTGGCTCACATCTGTAATCCCAACACTTTGGGAGGCTAAC ATTACCAAGAAGTGGGCTGGGCGTGGTGGCTC____________CCAACACTTTGGGAGGCTAAC GGATTACAGATGT G FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1564371231 Functional Loss DEL dbSNP153 33..44 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 49061 RMVar_ID_49061 Human_SNP_ID_416322604 A-to-I Human chr9 - 129939307 129939307 129939307 TCGGCTCACTGCAGCCTCTGCCTCGTGAGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTATC TCGGCTCACTGCAGCCTCTGCCTCGTGAGTTCTAGCGATTCTCCTGCCTCAGCCTCCCAAGTATC T A FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1199493512 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 49062 RMVar_ID_49062 Human_SNP_ID_416322765 A-to-I Human chr9 - 129939966 129939966 129939966 GAACTCCTGGCCTCAAGTGATCCTCCCACGTCAGCCTCCTCTAGTGCTGGGATTACAGGTGTGAG GAACTCCTGGCCTCAAGTGATCCTCCCACGTCGGCCTCCTCTAGTGCTGGGATTACAGGTGTGAG T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs895426139 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 49063 RMVar_ID_49063 Human_SNP_ID_416322802 A-to-I Human chr9 - 129940149 129940149 129940149 AAGCCCAGGCTGAAGTACAGTGGGACAATCATAGCTCACTATAGCCTCGAACTCCCGGGCTCAAG AAGCCCAGGCTGAAGTACAGTGGGACAATCATGGCTCACTATAGCCTCGAACTCCCGGGCTCAAG T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1488943830 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 49064 RMVar_ID_49064 Human_SNP_ID_416323083 A-to-I Human chr9 - 129941350 129941350 129941350 GCGTCTCGCTCTGTTGCCCAGGCTGGAGTGCAATGACGCAGTCTTGGCTCACTGCAGCCTCCACC GCGTCTCGCTCTGTTGCCCAGGCTGGAGTGCATTGACGCAGTCTTGGCTCACTGCAGCCTCCACC T A FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11790812 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 49065 RMVar_ID_49065 Human_SNP_ID_416323084 A-to-I Human chr9 - 129941350 129941350 129941350 GCGTCTCGCTCTGTTGCCCAGGCTGGAGTGCAATGACGCAGTCTTGGCTCACTGCAGCCTCCACC GCGTCTCGCTCTGTTGCCCAGGCTGGAGTGCAGTGACGCAGTCTTGGCTCACTGCAGCCTCCACC T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11790812 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 49066 RMVar_ID_49066 Human_SNP_ID_416323140 A-to-I Human chr9 - 129941542 129941542 129941542 ATCATTGCTTGAGCCTGGGAAGTTGAGGCTGCAGCGGGCTGTGATCATACCACTGCACTCCATCC ATCATTGCTTGAGCCTGGGAAGTTGAGGCTGCGGCGGGCTGTGATCATACCACTGCACTCCATCC T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1308627013 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 49067 RMVar_ID_49067 Human_SNP_ID_416323454 A-to-I Human chr9 - 129942968 129942968 129942968 GCCAAATGGGCCGGATGCAGTGGCTCATGCCTATAATTCTAGCATTTTGGGAGGCCAAGGCAGGA GCCAAATGGGCCGGATGCAGTGGCTCATGCCTGTAATTCTAGCATTTTGGGAGGCCAAGGCAGGA T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1225315057 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 49068 RMVar_ID_49068 Human_SNP_ID_416323615 A-to-I Human chr9 - 129943492 129943492 129943492 ATCTCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAAGCTGGGAGGCAAAGGTTGCAGTG ATCTCAGCTACTTGGGAGGCTGAGGCAGGAGACTCGCTTGAAGCTGGGAGGCAAAGGTTGCAGTG T G FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1454788448 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 49069 RMVar_ID_49069 Human_SNP_ID_416323621 A-to-I Human chr9 - 129943524 129943524 129943524 AAATTAGCTGGGCATGGTGGTGCACACCTGTAATCTCAGCTACTTGGGAGGCTGAGGCAGGAGAA AAATTAGCTGGGCATGGTGGTGCACACCTGTATTCTCAGCTACTTGGGAGGCTGAGGCAGGAGAA T A FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1425542088 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 49070 RMVar_ID_49070 Human_SNP_ID_416323660 A-to-I Human chr9 - 129943676 129943676 129943676 AATAGCAGTTTAAAAGCAATTAGGCCGGGCGCAGTGGCTCATGCCTGTAATCCCAGCACTTTAGG AATAGCAGTTTAAAAGCAATTAGGCCGGGCGCGGTGGCTCATGCCTGTAATCCCAGCACTTTAGG T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs972566190 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 49071 RMVar_ID_49071 Human_SNP_ID_416323668 A-to-I Human chr9 - 129943687 129943687 129943687 TGCCCGACCACAATAGCAGTTTAAAAGCAATTAGGCCGGGCGCAGTGGCTCATGCCTGTAATCCC TGCCCGACCACAATAGCAGTTTAAAAGCAATTTGGCCGGGCGCAGTGGCTCATGCCTGTAATCCC T A FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs186298145 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 49072 RMVar_ID_49072 Human_SNP_ID_416323683 A-to-I Human chr9 - 129943736 129943736 129943736 CTCCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTCAGCTACCGTGCCCGACCACAATAG CTCCCACCTCAGCCTCCCAAAGTGCTGGGATTCCAGGCGTCAGCTACCGTGCCCGACCACAATAG T G FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs946226725 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 49073 RMVar_ID_49073 Human_SNP_ID_416323689 A-to-I Human chr9 - 129943749 129943749 129943749 TGACCTCGTGATCCTCCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTCAGCTACCGTGC TGACCTCGTGATCCTCCCACCTCAGCCTCCCAGAGTGCTGGGATTACAGGCGTCAGCTACCGTGC T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1235443145 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 49074 RMVar_ID_49074 Human_SNP_ID_416323742 A-to-I Human chr9 - 129943947 129943947 129943947 GCTCTGTCGCCCAGGCTGGAGTGCAGTGGTGCAGTCTTGGCTCACTGCAAGCTCTGCTTCCCAGG GCTCTGTCGCCCAGGCTGGAGTGCAGTGGTGCGGTCTTGGCTCACTGCAAGCTCTGCTTCCCAGG T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1357014077 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 49075 RMVar_ID_49075 Human_SNP_ID_416324009 A-to-I Human chr9 - 129944885 129944883 129944885 GTAAGTCATTTAATAAGGTATTTTAATTTTCAATGATAGTAAATGGCCTAGCCCATGGCTAAGAG GTAAGTCATTTAATAAGGTATTTTAATTTTCAGTAATAGTAAATGGCCTAGCCCATGGCTAAGAG CAT TAC FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs386738862 Functional Loss MNV dbSNP153 33..35 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 49076 RMVar_ID_49076 Human_SNP_ID_416324011 A-to-I Human chr9 - 129944885 129944885 129944885 GTAAGTCATTTAATAAGGTATTTTAATTTTCAATGATAGTAAATGGCCTAGCCCATGGCTAAGAG GTAAGTCATTTAATAAGGTATTTTAATTTTCAGTGATAGTAAATGGCCTAGCCCATGGCTAAGAG T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7870884 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_6079,GWAS_ID_6080,GWAS_ID_6081,GWAS_ID_6082,GWAS_ID_6083,GWAS_ID_6084,GWAS_ID_6085,GWAS_ID_6086,GWAS_ID_6087,GWAS_ID_6088 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 49077 RMVar_ID_49077 Human_SNP_ID_416324517 A-to-I Human chr9 - 129947324 129947324 129947324 GCAATTCTCCTTTCTCAGCCTCCCAAATAGCTAAGATTACAGGCGCCTGCCACCACACCCGGCTA GCAATTCTCCTTTCTCAGCCTCCCAAATAGCTGAGATTACAGGCGCCTGCCACCACACCCGGCTA T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1564402742 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 49078 RMVar_ID_49078 Human_SNP_ID_416324656 A-to-I Human chr9 - 129947787 129947787 129947787 AGAAACCCTGTCTCTACTAAAAATACAAAATTAGCCAGGTGTGGTGGCGCATGCCTGTAATGTCA AGAAACCCTGTCTCTACTAAAAATACAAAATTTGCCAGGTGTGGTGGCGCATGCCTGTAATGTCA T A FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs989701552 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 49079 RMVar_ID_49079 Human_SNP_ID_416324727 A-to-I Human chr9 - 129948071 129948071 129948071 GTTCCCAGGCTGGTCTTGAACTCCTAGCCTCAAGTGATCCTCCTGCCTCAGCTTCACAAAGTGCT GTTCCCAGGCTGGTCTTGAACTCCTAGCCTCAGGTGATCCTCCTGCCTCAGCTTCACAAAGTGCT T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1399663106 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 49080 RMVar_ID_49080 Human_SNP_ID_416324749 A-to-I Human chr9 - 129948190 129948190 129948190 AAACTTATTGCAGCCTCAACCTCGTGGATTCAAGTGATCCTCCTGCCTCAGCCTCCCAAGTAGCT AAACTTATTGCAGCCTCAACCTCGTGGATTCATGTGATCCTCCTGCCTCAGCCTCCCAAGTAGCT T A FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1564405103 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 49081 RMVar_ID_49081 Human_SNP_ID_416324906 A-to-I Human chr9 - 129948681 129948681 129948681 AAAATTAGCCGGGCATGGTGGCACGTGCCTGTAATCCCAGCTATTTGGGAGGCTAAGGCAGGAGA AAAATTAGCCGGGCATGGTGGCACGTGCCTGTGATCCCAGCTATTTGGGAGGCTAAGGCAGGAGA T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1202552519 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 49082 RMVar_ID_49082 Human_SNP_ID_416325484 A-to-I Human chr9 - 129951160 129951160 129951160 CTGAGATCAGGGGTTTGAGACCAGCCTAGCCAACATGGTGAAACTTCATCTCTACAAAAAATACA CTGAGATCAGGGGTTTGAGACCAGCCTAGCCATCATGGTGAAACTTCATCTCTACAAAAAATACA T A FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1030085116 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 49083 RMVar_ID_49083 Human_SNP_ID_416325503 A-to-I Human chr9 - 129951248 129951248 129951248 TTCTACAAAATAATCAAAAAATTAGACCGGGCATGGTGGCTCACGCATGTGATGCCAGCACTATG TTCTACAAAATAATCAAAAAATTAGACCGGGCGTGGTGGCTCACGCATGTGATGCCAGCACTATG T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs928742092 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 49084 RMVar_ID_49084 Human_SNP_ID_416325510 A-to-I Human chr9 - 129951257 129951257 129951257 AAACCCAGTTTCTACAAAATAATCAAAAAATTAGACCGGGCATGGTGGCTCACGCATGTGATGCC AAACCCAGTTTCTACAAAATAATCAAAAAATTGGACCGGGCATGGTGGCTCACGCATGTGATGCC T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10732399 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_6089,GWAS_ID_6090,GWAS_ID_6091,GWAS_ID_6092,GWAS_ID_6093,GWAS_ID_6094,GWAS_ID_6095,GWAS_ID_6096,GWAS_ID_6097,GWAS_ID_6098,GWAS_ID_6099,GWAS_ID_6100,GWAS_ID_6101,GWAS_ID_6102,GWAS_ID_6103,GWAS_ID_6104,GWAS_ID_6105 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 49085 RMVar_ID_49085 Human_SNP_ID_416325522 A-to-I Human chr9 - 129951336 129951336 129951336 TCATCCTAGCACTTTGGGAGGCTGAGGCAGGAAGAGTGCTGGAGGCTAGGAGTTCAAGACCAGCC TCATCCTAGCACTTTGGGAGGCTGAGGCAGGAGGAGTGCTGGAGGCTAGGAGTTCAAGACCAGCC T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10739767 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1118316 GWAS_ID_6106,GWAS_ID_6107,GWAS_ID_6108,GWAS_ID_6109,GWAS_ID_6110,GWAS_ID_6111,GWAS_ID_6112,GWAS_ID_6113,GWAS_ID_6114,GWAS_ID_6115,GWAS_ID_6116,GWAS_ID_6117,GWAS_ID_6118,GWAS_ID_6119,GWAS_ID_6120,GWAS_ID_6121,GWAS_ID_6122 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 49086 RMVar_ID_49086 Human_SNP_ID_416325653 A-to-I Human chr9 - 129951734 129951734 129951734 CCCCATATAAGAAGTCATATAAAGCTGGGTATAGTGGCTCATGCCTGTAATCCCAGCCCTTTGGA CCCCATATAAGAAGTCATATAAAGCTGGGTATGGTGGCTCATGCCTGTAATCCCAGCCCTTTGGA T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs868154788 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 49087 RMVar_ID_49087 Human_SNP_ID_416325798 A-to-I Human chr9 - 129952314 129952314 129952314 TCATGTTTTTAGTAGAGACGAGGTTTCACCATATTGCCAGGCTGGTCTCGAACCCCTGACCTCAG TCATGTTTTTAGTAGAGACGAGGTTTCACCATGTTGCCAGGCTGGTCTCGAACCCCTGACCTCAG T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1203675020 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 49088 RMVar_ID_49088 Human_SNP_ID_416325837 A-to-I Human chr9 - 129952467 129952467 129952467 TGTTTTTTGAGTCTCACTCTGTCGCCCAGGCTAGAGTGCAGTGGCATGATCTCCACTCACTTCAA TGTTTTTTGAGTCTCACTCTGTCGCCCAGGCTGGAGTGCAGTGGCATGATCTCCACTCACTTCAA T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1296105634 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 49089 RMVar_ID_49089 Human_SNP_ID_416326515 A-to-I Human chr9 - 129955639 129955639 129955639 TTGGCTAACAACAACCTCTGTCTTCAGGGCTCAAGTGATCCTCCTGCCTCAGCCTCCTGAGTAGC TTGGCTAACAACAACCTCTGTCTTCAGGGCTCGAGTGATCCTCCTGCCTCAGCCTCCTGAGTAGC T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1477214285 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 49090 RMVar_ID_49090 Human_SNP_ID_416327194 A-to-I Human chr9 - 129958302 129958302 129958302 TCAGCCTCCCAAGTAGCTAAGATTACAGGCACACGTCACCATGCCCGGCTAATTTTTGTATTTTT TCAGCCTCCCAAGTAGCTAAGATTACAGGCACGCGTCACCATGCCCGGCTAATTTTTGTATTTTT T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1280497208 Functional Loss SNV dbSNP153 33..33 33 - - - 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_55216,RMVar_hsa_circ_30836,RMVar_hsa_circ_269261,RMVar_hsa_circ_260285,RMVar_hsa_circ_260287,RMVar_hsa_circ_288850,RMVar_hsa_circ_373911,RMVar_hsa_circ_283777,RMVar_hsa_circ_260286 49091 RMVar_ID_49091 Human_SNP_ID_416327219 A-to-I Human chr9 - 129958393 129958393 129958393 GAGGCTCCCTCTGTTGCCCAGGTTGGAGTGCAATGGTGCGATCTCGGCTCACTGTAACCTCTGCT GAGGCTCCCTCTGTTGCCCAGGTTGGAGTGCAGTGGTGCGATCTCGGCTCACTGTAACCTCTGCT T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs571745472 Functional Loss SNV dbSNP153 33..33 33 - - - 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_55216,RMVar_hsa_circ_30836,RMVar_hsa_circ_269261,RMVar_hsa_circ_260285,RMVar_hsa_circ_260287,RMVar_hsa_circ_288850,RMVar_hsa_circ_373911,RMVar_hsa_circ_283777,RMVar_hsa_circ_260286 49092 RMVar_ID_49092 Human_SNP_ID_416328025 A-to-I Human chr9 - 129961156 129961156 129961156 GGCATGCGCCACCATGCCTGGCTACTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGC GGCATGCGCCACCATGCCTGGCTACTTTTTGTGTTTTTAGTAGAGACGGGGTTTCACCATGTTGC T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs962201786 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116881,RMVar_hsa_circ_260269,RMVar_hsa_circ_69780,RMVar_hsa_circ_359498,RMVar_hsa_circ_55216,RMVar_hsa_circ_30836,RMVar_hsa_circ_260287,RMVar_hsa_circ_288850,RMVar_hsa_circ_373911,RMVar_hsa_circ_260286 49093 RMVar_ID_49093 Human_SNP_ID_416328157 A-to-I Human chr9 - 129961653 129961653 129961653 TTGAACCCGGGAGGCAGAGGTCACAGGGAGGCAGAGGTCTCAGTGAACCGAGATCACGCCACTGT TTGAACCCGGGAGGCAGAGGTCACAGGGAGGCGGAGGTCTCAGTGAACCGAGATCACGCCACTGT T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs906689799 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116881,RMVar_hsa_circ_260269,RMVar_hsa_circ_69780,RMVar_hsa_circ_359498,RMVar_hsa_circ_55216,RMVar_hsa_circ_30836,RMVar_hsa_circ_260287,RMVar_hsa_circ_288850,RMVar_hsa_circ_373911,RMVar_hsa_circ_260286 49094 RMVar_ID_49094 Human_SNP_ID_416328175 A-to-I Human chr9 - 129961713 129961711 129961713 GGGCGTGGTGGGTCGCACCTGTATTCCCAGCTACCAGGGAGGCTGAGGCAGGAGAATCACTTGAA GGGCGTGGTGGGTCGCACCTGTATTCCCAGCT__CAGGGAGGCTGAGGCAGGAGAATCACTTGAA GGT G FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1318254733 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_116881,RMVar_hsa_circ_260269,RMVar_hsa_circ_69780,RMVar_hsa_circ_359498,RMVar_hsa_circ_55216,RMVar_hsa_circ_30836,RMVar_hsa_circ_260287,RMVar_hsa_circ_288850,RMVar_hsa_circ_373911,RMVar_hsa_circ_260286 49095 RMVar_ID_49095 Human_SNP_ID_416330617 A-to-I Human chr9 - 129971133 129971133 129971133 TAATCCCAGAACTTTGGGAGGCGGAGGTGGGCATATCAAAAGGTCAGGAGTTCCAGACCAGCCTG TAATCCCAGAACTTTGGGAGGCGGAGGTGGGCGTATCAAAAGGTCAGGAGTTCCAGACCAGCCTG T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6478933 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116881,RMVar_hsa_circ_260269,RMVar_hsa_circ_69780,RMVar_hsa_circ_359498,RMVar_hsa_circ_55216,RMVar_hsa_circ_30836,RMVar_hsa_circ_260287,RMVar_hsa_circ_288850,RMVar_hsa_circ_373911,RMVar_hsa_circ_260286 49096 RMVar_ID_49096 Human_SNP_ID_416331625 A-to-I Human chr9 - 129975175 129975175 129975175 TCGCTCTGTTGCCCGGGCTGGAGTGCAGTTGCACAAACTCGGCTTACTGCAGCCTCCGCCTTCTG TCGCTCTGTTGCCCGGGCTGGAGTGCAGTTGCGCAAACTCGGCTTACTGCAGCCTCCGCCTTCTG T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1002346497 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116881,RMVar_hsa_circ_260269,RMVar_hsa_circ_69780,RMVar_hsa_circ_359498,RMVar_hsa_circ_55216,RMVar_hsa_circ_30836,RMVar_hsa_circ_260287,RMVar_hsa_circ_288850,RMVar_hsa_circ_373911,RMVar_hsa_circ_260286 49097 RMVar_ID_49097 Human_SNP_ID_416331742 A-to-I Human chr9 - 129975816 129975816 129975816 TAACCACAACCTCCACCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGA TAACCACAACCTCCACCTCCCAGGTTCAAGCGGTTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGA T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1345998090 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116881,RMVar_hsa_circ_260269,RMVar_hsa_circ_69780,RMVar_hsa_circ_359498,RMVar_hsa_circ_55216,RMVar_hsa_circ_30836,RMVar_hsa_circ_260287,RMVar_hsa_circ_288850,RMVar_hsa_circ_373911,RMVar_hsa_circ_260286 49098 RMVar_ID_49098 Human_SNP_ID_416332726 A-to-I Human chr9 - 129979907 129979907 129979907 CGGGCACCGTGGCTCACACCTGTGATCCCAGCACTTTGGGAGGCCAAGGCAGGCAGATCATTTGA CGGGCACCGTGGCTCACACCTGTGATCCCAGCGCTTTGGGAGGCCAAGGCAGGCAGATCATTTGA T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1273806111 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69780,RMVar_hsa_circ_359498,RMVar_hsa_circ_55216,RMVar_hsa_circ_30836,RMVar_hsa_circ_260288,RMVar_hsa_circ_260287,RMVar_hsa_circ_288850,RMVar_hsa_circ_299047,RMVar_hsa_circ_260289 49099 RMVar_ID_49099 Human_SNP_ID_416332784 A-to-I Human chr9 - 129980163 129980163 129980163 TAGGGACGGGGTTTCTCCATGTTGGTCAGGCCAGTCTCGAACTTCCAACCTCAGGTGATCTGTCT TAGGGACGGGGTTTCTCCATGTTGGTCAGGCCGGTCTCGAACTTCCAACCTCAGGTGATCTGTCT T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1250104423 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69780,RMVar_hsa_circ_359498,RMVar_hsa_circ_55216,RMVar_hsa_circ_30836,RMVar_hsa_circ_260288,RMVar_hsa_circ_260287,RMVar_hsa_circ_288850,RMVar_hsa_circ_299047,RMVar_hsa_circ_260289 49100 RMVar_ID_49100 Human_SNP_ID_416332886 A-to-I Human chr9 - 129980604 129980604 129980604 TGAATATAAAGAAAAATATTTAGATTCTTAACATGGAGATGAGATTAGGAAGGGAAACTAGGATG TGAATATAAAGAAAAATATTTAGATTCTTAACGTGGAGATGAGATTAGGAAGGGAAACTAGGATG T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10733706 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69780,RMVar_hsa_circ_359498,RMVar_hsa_circ_55216,RMVar_hsa_circ_30836,RMVar_hsa_circ_260288,RMVar_hsa_circ_260287,RMVar_hsa_circ_288850,RMVar_hsa_circ_299047,RMVar_hsa_circ_260289 49101 RMVar_ID_49101 Human_SNP_ID_416333316 A-to-I Human chr9 - 129982210 129982210 129982210 CCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCGCCCGGCCCCCTTTCATTCTT CCTTGGCCTCCCAAAGTGCTGGGATTACAGGCTTGAGCCACCGCGCCCGGCCCCCTTTCATTCTT T A FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4837438 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69780,RMVar_hsa_circ_359498,RMVar_hsa_circ_55216,RMVar_hsa_circ_30836,RMVar_hsa_circ_260288,RMVar_hsa_circ_260287,RMVar_hsa_circ_288850,RMVar_hsa_circ_299047,RMVar_hsa_circ_260289 49102 RMVar_ID_49102 Human_SNP_ID_416333317 A-to-I Human chr9 - 129982210 129982210 129982210 CCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCGCCCGGCCCCCTTTCATTCTT CCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCCCGGCCCCCTTTCATTCTT T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4837438 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69780,RMVar_hsa_circ_359498,RMVar_hsa_circ_55216,RMVar_hsa_circ_30836,RMVar_hsa_circ_260288,RMVar_hsa_circ_260287,RMVar_hsa_circ_288850,RMVar_hsa_circ_299047,RMVar_hsa_circ_260289 49103 RMVar_ID_49103 Human_SNP_ID_416333737 A-to-I Human chr9 - 129984031 129984031 129984031 AAGTCATTTTTAAAGCCTTCCTGTGGTTCTTCAAATCAGCCAGGTCTAAATCCACCATCCTTATA AAGTCATTTTTAAAGCCTTCCTGTGGTTCTTCTAATCAGCCAGGTCTAAATCCACCATCCTTATA T A FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4837441 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69780,RMVar_hsa_circ_359498,RMVar_hsa_circ_55216,RMVar_hsa_circ_30836,RMVar_hsa_circ_260288,RMVar_hsa_circ_260287,RMVar_hsa_circ_288850,RMVar_hsa_circ_299047,RMVar_hsa_circ_260289 49104 RMVar_ID_49104 Human_SNP_ID_416333738 A-to-I Human chr9 - 129984031 129984031 129984031 AAGTCATTTTTAAAGCCTTCCTGTGGTTCTTCAAATCAGCCAGGTCTAAATCCACCATCCTTATA AAGTCATTTTTAAAGCCTTCCTGTGGTTCTTCGAATCAGCCAGGTCTAAATCCACCATCCTTATA T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4837441 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69780,RMVar_hsa_circ_359498,RMVar_hsa_circ_55216,RMVar_hsa_circ_30836,RMVar_hsa_circ_260288,RMVar_hsa_circ_260287,RMVar_hsa_circ_288850,RMVar_hsa_circ_299047,RMVar_hsa_circ_260289 49105 RMVar_ID_49105 Human_SNP_ID_416334069 A-to-I Human chr9 - 129985427 129985427 129985427 CTGGTTCTTCCACTTAACAGCCATATGAATTGAGTTAAATTACTCTCCTTGTTTCATGATTTTCA CTGGTTCTTCCACTTAACAGCCATATGAATTGTGTTAAATTACTCTCCTTGTTTCATGATTTTCA T A FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10122287 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69780,RMVar_hsa_circ_359498,RMVar_hsa_circ_55216,RMVar_hsa_circ_30836,RMVar_hsa_circ_260288,RMVar_hsa_circ_260287,RMVar_hsa_circ_288850,RMVar_hsa_circ_299047,RMVar_hsa_circ_260289 49106 RMVar_ID_49106 Human_SNP_ID_416334070 A-to-I Human chr9 - 129985427 129985427 129985427 CTGGTTCTTCCACTTAACAGCCATATGAATTGAGTTAAATTACTCTCCTTGTTTCATGATTTTCA CTGGTTCTTCCACTTAACAGCCATATGAATTGGGTTAAATTACTCTCCTTGTTTCATGATTTTCA T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10122287 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69780,RMVar_hsa_circ_359498,RMVar_hsa_circ_55216,RMVar_hsa_circ_30836,RMVar_hsa_circ_260288,RMVar_hsa_circ_260287,RMVar_hsa_circ_288850,RMVar_hsa_circ_299047,RMVar_hsa_circ_260289 49107 RMVar_ID_49107 Human_SNP_ID_416334071 A-to-I Human chr9 - 129985427 129985427 129985427 CTGGTTCTTCCACTTAACAGCCATATGAATTGAGTTAAATTACTCTCCTTGTTTCATGATTTTCA CTGGTTCTTCCACTTAACAGCCATATGAATTGCGTTAAATTACTCTCCTTGTTTCATGATTTTCA T G FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10122287 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69780,RMVar_hsa_circ_359498,RMVar_hsa_circ_55216,RMVar_hsa_circ_30836,RMVar_hsa_circ_260288,RMVar_hsa_circ_260287,RMVar_hsa_circ_288850,RMVar_hsa_circ_299047,RMVar_hsa_circ_260289 49108 RMVar_ID_49108 Human_SNP_ID_416334558 A-to-I Human chr9 - 129987384 129987384 129987384 ATACATGTTTTGCTCCTTCTTCTAGTTGAGTTATATGACTGGGTTCTGAAACCCGAGGCCCTCAG ATACATGTTTTGCTCCTTCTTCTAGTTGAGTTGTATGACTGGGTTCTGAAACCCGAGGCCCTCAG T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10739770 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69780,RMVar_hsa_circ_359498,RMVar_hsa_circ_55216,RMVar_hsa_circ_30836,RMVar_hsa_circ_260288,RMVar_hsa_circ_260287,RMVar_hsa_circ_288850,RMVar_hsa_circ_299047,RMVar_hsa_circ_260289 49109 RMVar_ID_49109 Human_SNP_ID_416335381 A-to-I Human chr9 - 129991255 129991255 129991255 AAAAAAAAAAAATCTGCATTTCCACGACCTAGATTTTCCTCCACTCACCTGAGGGTAGCTGCATC AAAAAAAAAAAATCTGCATTTCCACGACCTAGGTTTTCCTCCACTCACCTGAGGGTAGCTGCATC T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2102209 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_6123,GWAS_ID_6124,GWAS_ID_6125,GWAS_ID_6126,GWAS_ID_6127,GWAS_ID_6128,GWAS_ID_6129,GWAS_ID_6130,GWAS_ID_6131,GWAS_ID_6132 RMVar_hsa_circ_69780,RMVar_hsa_circ_359498,RMVar_hsa_circ_55216,RMVar_hsa_circ_30836,RMVar_hsa_circ_260288,RMVar_hsa_circ_260287,RMVar_hsa_circ_288850,RMVar_hsa_circ_299047,RMVar_hsa_circ_260289 49110 RMVar_ID_49110 Human_SNP_ID_416335448 A-to-I Human chr9 - 129991472 129991472 129991472 GCCCAGGAGTTGGAGGCCAGCCTGAGCAACATAGCGAGACCCTGCCTCTAAAAAGAATTTTAAAA GCCCAGGAGTTGGAGGCCAGCCTGAGCAACATGGCGAGACCCTGCCTCTAAAAAGAATTTTAAAA T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs946816621 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69780,RMVar_hsa_circ_359498,RMVar_hsa_circ_55216,RMVar_hsa_circ_30836,RMVar_hsa_circ_260288,RMVar_hsa_circ_260287,RMVar_hsa_circ_288850,RMVar_hsa_circ_299047,RMVar_hsa_circ_260289 49111 RMVar_ID_49111 Human_SNP_ID_416335541 A-to-I Human chr9 - 129991798 129991798 129991798 AAAATTAGCTGGAAATGGTGGCGGGCGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA AAAATTAGCTGGAAATGGTGGCGGGCGCCTGTGGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1335502210 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69780,RMVar_hsa_circ_359498,RMVar_hsa_circ_55216,RMVar_hsa_circ_30836,RMVar_hsa_circ_260288,RMVar_hsa_circ_260287,RMVar_hsa_circ_288850,RMVar_hsa_circ_299047,RMVar_hsa_circ_260289 49112 RMVar_ID_49112 Human_SNP_ID_416336788 A-to-I Human chr9 - 129996974 129996974 129996974 AAAAAACAGGCCGGCCGGAGGCAGTGGCTCACACTTGTAATCCCAGCACTTTGGGATGCCAAGGC AAAAAACAGGCCGGCCGGAGGCAGTGGCTCACGCTTGTAATCCCAGCACTTTGGGATGCCAAGGC T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1412756712 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_260288 49113 RMVar_ID_49113 Human_SNP_ID_416341316 A-to-I Human chr9 - 130015753 130015753 130015753 GGAGGATCACCTGAGCCCAGGAGGTTGAGGTTACAGCGAGCCGAAATTGTGCCAATGCATTCCAG GGAGGATCACCTGAGCCCAGGAGGTTGAGGTTCCAGCGAGCCGAAATTGTGCCAATGCATTCCAG T G FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1203004362 Functional Loss SNV dbSNP153 33..33 33 - - - 49114 RMVar_ID_49114 Human_SNP_ID_416341342 A-to-I Human chr9 - 130015863 130015863 130015863 CAAGACCAGCCTGGGCAATATGGCAAAACCCCATCTCTACAAAAGATACAAAAATTAGCCAGGCA CAAGACCAGCCTGGGCAATATGGCAAAACCCCCTCTCTACAAAAGATACAAAAATTAGCCAGGCA T G FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs996119835 Functional Loss SNV dbSNP153 33..33 33 - - - 49115 RMVar_ID_49115 Human_SNP_ID_416341544 A-to-I Human chr9 - 130016738 130016738 130016738 AAATATTTTCTTTTCTTTTCTTTTTTTGAGACAGAGTTTTGCTCTTGTTGTCCAGGCTAGAGTGC AAATATTTTCTTTTCTTTTCTTTTTTTGAGACGGAGTTTTGCTCTTGTTGTCCAGGCTAGAGTGC T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs547906408 Functional Loss SNV dbSNP153 33..33 33 - - - 49116 RMVar_ID_49116 Human_SNP_ID_416341739 A-to-I Human chr9 - 130017647 130017647 130017647 TTTTGTATTTTTAGTAGAGACTGGGTTTCGCGATGTTGGCCAGGCTGGTCTTGAACTCCCAACCT TTTTGTATTTTTAGTAGAGACTGGGTTTCGCGTTGTTGGCCAGGCTGGTCTTGAACTCCCAACCT T A FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs927296226 Functional Loss SNV dbSNP153 33..33 33 - - - 49117 RMVar_ID_49117 Human_SNP_ID_416341740 A-to-I Human chr9 - 130017647 130017647 130017647 TTTTGTATTTTTAGTAGAGACTGGGTTTCGCGATGTTGGCCAGGCTGGTCTTGAACTCCCAACCT TTTTGTATTTTTAGTAGAGACTGGGTTTCGCGGTGTTGGCCAGGCTGGTCTTGAACTCCCAACCT T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs927296226 Functional Loss SNV dbSNP153 33..33 33 - - - 49118 RMVar_ID_49118 Human_SNP_ID_416341759 A-to-I Human chr9 - 130017747 130017747 130017747 TAGCTCACTGCAACCTCTGCCTTCCGGGTTCAAGTGATTCTCCTGCCTTAGCCTCCAGAGTAGCT TAGCTCACTGCAACCTCTGCCTTCCGGGTTCAGGTGATTCTCCTGCCTTAGCCTCCAGAGTAGCT T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs940534350 Functional Loss SNV dbSNP153 33..33 33 - - - 49119 RMVar_ID_49119 Human_SNP_ID_416341892 A-to-I Human chr9 - 130018091 130018091 130018091 GCTAACACAGTGAAACTCTGTCTCTACTAAAAATATTAAAAAATTAGCCAGGCGTGGTGGCAGGT GCTAACACAGTGAAACTCTGTCTCTACTAAAACTATTAAAAAATTAGCCAGGCGTGGTGGCAGGT T G FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1222259971 Functional Loss SNV dbSNP153 33..33 33 - - - 49120 RMVar_ID_49120 Human_SNP_ID_416342116 A-to-I Human chr9 - 130019105 130019105 130019105 CTCCCACCTCGGCCTCCTGAGTAGCTGGGACCACAGATGCAGGCCACCATGCCCGGCTAATTTTT CTCCCACCTCGGCCTCCTGAGTAGCTGGGACCGCAGATGCAGGCCACCATGCCCGGCTAATTTTT T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1224646347 Functional Loss SNV dbSNP153 33..33 33 - - - 49121 RMVar_ID_49121 Human_SNP_ID_416343333 A-to-I Human chr9 - 130024334 130024334 130024334 GCCATCCTCCCACTTCAGCCTCCCCAGTAGCTAAGACTCAGGTGCACACTACCACGCCCAGCTAA GCCATCCTCCCACTTCAGCCTCCCCAGTAGCTGAGACTCAGGTGCACACTACCACGCCCAGCTAA T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs559196931 Functional Loss SNV dbSNP153 33..33 33 - - - 49122 RMVar_ID_49122 Human_SNP_ID_416345077 A-to-I Human chr9 - 130032291 130032291 130032291 TGGTGCATGCCTGTAGTCCCAGCTACTTGGGAAGCTGAGATGGGAGGATCACTTCAGACCAGGAG TGGTGCATGCCTGTAGTCCCAGCTACTTGGGACGCTGAGATGGGAGGATCACTTCAGACCAGGAG T G FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs572531339 Functional Loss SNV dbSNP153 33..33 33 - - - 49123 RMVar_ID_49123 Human_SNP_ID_416345086 A-to-I Human chr9 - 130032325 130032325 130032325 CTCTACTAAAAATTAAAAAATTACCTGGGCATAGTGGTGCATGCCTGTAGTCCCAGCTACTTGGG CTCTACTAAAAATTAAAAAATTACCTGGGCATGGTGGTGCATGCCTGTAGTCCCAGCTACTTGGG T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1360405979 Functional Loss SNV dbSNP153 33..33 33 - - - 49124 RMVar_ID_49124 Human_SNP_ID_416345571 A-to-I Human chr9 - 130034154 130034154 130034154 CGTTTGCCCGGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACAGTGTTAGCCAGGATGG CGTTTGCCCGGCTAATTTTTTGTATTTTTAGTGGAGACGGGGTTTCACAGTGTTAGCCAGGATGG T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1298299035 Functional Loss SNV dbSNP153 33..33 33 - - - 49125 RMVar_ID_49125 Human_SNP_ID_416352159 A-to-I Human chr9 + 130058520 130058520 130058520 GGAGTCTCGGACTGTTGCCTAGGCTGGAGCGCAATGGCGTTATCTCGGCTCACTGCAACCTCTAC GGAGTCTCGGACTGTTGCCTAGGCTGGAGCGCGATGGCGTTATCTCGGCTCACTGCAACCTCTAC A G GPR107 Ensembl:ENSG00000148358 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1469793100 Functional Loss SNV dbSNP153 33..33 33 - - - 49126 RMVar_ID_49126 Human_SNP_ID_416354078 A-to-I Human chr9 + 130065193 130065193 130065193 ATATTCGCAGCCGGGCACGGTGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCCGAGGTGGGC ATATTCGCAGCCGGGCACGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGC A G GPR107 Ensembl:ENSG00000148358 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1414718882 Functional Loss SNV dbSNP153 33..33 33 - - - 49127 RMVar_ID_49127 Human_SNP_ID_416354079 A-to-I Human chr9 + 130065195 130065195 130065195 ATTCGCAGCCGGGCACGGTGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCCGAGGTGGGCAA ATTCGCAGCCGGGCACGGTGGCTCATGCCTATGATCCCAGCACTTTGGGAGGCCGAGGTGGGCAA A G GPR107 Ensembl:ENSG00000148358 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1416677181 Functional Loss SNV dbSNP153 33..33 33 - - - 49128 RMVar_ID_49128 Human_SNP_ID_416354798 A-to-I Human chr9 + 130067844 130067844 130067844 TTGGCTCACTGCAACCTTTGCCTCCCAAGTCCAAGTGATCCTCCTGCCCCAGCCTCCCAAGCAGC TTGGCTCACTGCAACCTTTGCCTCCCAAGTCCCAGTGATCCTCCTGCCCCAGCCTCCCAAGCAGC A C GPR107 Ensembl:ENSG00000148358 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1347621987 Functional Loss SNV dbSNP153 33..33 33 - - - 49129 RMVar_ID_49129 Human_SNP_ID_416354830 A-to-I Human chr9 + 130067974 130067974 130067974 ACCATATTGGCCAGGCTCAAACTTCTGACTTCAAGTGATCCTCCCACCTCAGCCCCCCAAAGTGC ACCATATTGGCCAGGCTCAAACTTCTGACTTCTAGTGATCCTCCCACCTCAGCCCCCCAAAGTGC A T GPR107 Ensembl:ENSG00000148358 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs552732653 Functional Loss SNV dbSNP153 33..33 33 - - - 49130 RMVar_ID_49130 Human_SNP_ID_416356131 A-to-I Human chr9 + 130072493 130072493 130072493 TGCCTGCCTCGGCCTCCCAAAGTGCCGGGATTACAGGTGTGAGCCACCGCGCCCGGCCTTGATCT TGCCTGCCTCGGCCTCCCAAAGTGCCGGGATTGCAGGTGTGAGCCACCGCGCCCGGCCTTGATCT A G GPR107 Ensembl:ENSG00000148358 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs867675442 Functional Loss SNV dbSNP153 33..33 33 - - - 49131 RMVar_ID_49131 Human_SNP_ID_416358546 A-to-I Human chr9 + 130081562 130081562 130081562 GGGCATGGTGGCACGTGCCTGTGATCTCAGCTACTCAGGAGACTGAGGCAGGAGAATTGCTTGGA GGGCATGGTGGCACGTGCCTGTGATCTCAGCTCCTCAGGAGACTGAGGCAGGAGAATTGCTTGGA A C GPR107 Ensembl:ENSG00000148358 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs923729594 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21531,RMVar_hsa_circ_41437,RMVar_hsa_circ_323274,RMVar_hsa_circ_340650,RMVar_hsa_circ_320368,RMVar_hsa_circ_45863,RMVar_hsa_circ_260291,RMVar_hsa_circ_330406,RMVar_hsa_circ_343175,RMVar_hsa_circ_260293,RMVar_hsa_circ_52821,RMVar_hsa_circ_349734,RMVar_hsa_circ_260292,RMVar_hsa_circ_302690,RMVar_hsa_circ_260296,RMVar_hsa_circ_113198,RMVar_hsa_circ_308885,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_260295 49132 RMVar_ID_49132 Human_SNP_ID_416358548 A-to-I Human chr9 + 130081566 130081566 130081566 ATGGTGGCACGTGCCTGTGATCTCAGCTACTCAGGAGACTGAGGCAGGAGAATTGCTTGGACCAG ATGGTGGCACGTGCCTGTGATCTCAGCTACTCGGGAGACTGAGGCAGGAGAATTGCTTGGACCAG A G GPR107 Ensembl:ENSG00000148358 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1246875665 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21531,RMVar_hsa_circ_41437,RMVar_hsa_circ_323274,RMVar_hsa_circ_340650,RMVar_hsa_circ_320368,RMVar_hsa_circ_45863,RMVar_hsa_circ_260291,RMVar_hsa_circ_330406,RMVar_hsa_circ_343175,RMVar_hsa_circ_260293,RMVar_hsa_circ_52821,RMVar_hsa_circ_349734,RMVar_hsa_circ_260292,RMVar_hsa_circ_302690,RMVar_hsa_circ_260296,RMVar_hsa_circ_113198,RMVar_hsa_circ_308885,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_260295 49133 RMVar_ID_49133 Human_SNP_ID_416360095 A-to-I Human chr9 + 130087210 130087210 130087210 CAGGCATAGACCACCATACCTGGCTAATTTTTAAATTTTTTGTAGAGATGAGGTCTTGCTCTGTT CAGGCATAGACCACCATACCTGGCTAATTTTTTAATTTTTTGTAGAGATGAGGTCTTGCTCTGTT A T GPR107 Ensembl:ENSG00000148358 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1312430843 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21531,RMVar_hsa_circ_41437,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_15732,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_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_377767,RMVar_hsa_circ_10910,RMVar_hsa_circ_291588,RMVar_hsa_circ_260301,RMVar_hsa_circ_260302 49134 RMVar_ID_49134 Human_SNP_ID_416364840 A-to-I Human chr9 + 130105934 130105934 130105934 TTCCCACCTCAGCCTCCCAAAGTGCTGGGATTATAGGCATGAGCCACCGCACCCAGTGGAATATG TTCCCACCTCAGCCTCCCAAAGTGCTGGGATTTTAGGCATGAGCCACCGCACCCAGTGGAATATG A T GPR107 Ensembl:ENSG00000148358 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1477062324 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_461,RMVar_hsa_circ_41437,RMVar_hsa_circ_326380,RMVar_hsa_circ_337763,RMVar_hsa_circ_316315,RMVar_hsa_circ_305589,RMVar_hsa_circ_260300,RMVar_hsa_circ_260299,RMVar_hsa_circ_377767,RMVar_hsa_circ_260301,RMVar_hsa_circ_322279,RMVar_hsa_circ_30145,RMVar_hsa_circ_357237,RMVar_hsa_circ_116022,RMVar_hsa_circ_333683,RMVar_hsa_circ_260305,RMVar_hsa_circ_260306,RMVar_hsa_circ_4877,RMVar_hsa_circ_64170 49135 RMVar_ID_49135 Human_SNP_ID_416366645 A-to-I Human chr9 + 130113015 130113015 130113015 CAAGTGATCCACCCACCTAGGCCTCCCAGAGTACTGAGATAACAGGCATGAGCCACTGTGCCTGG CAAGTGATCCACCCACCTAGGCCTCCCAGAGTGCTGAGATAACAGGCATGAGCCACTGTGCCTGG A G GPR107 Ensembl:ENSG00000148358 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1227755385 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16591463 RMVar_hsa_circ_326380,RMVar_hsa_circ_316315,RMVar_hsa_circ_260300,RMVar_hsa_circ_377767,RMVar_hsa_circ_260301,RMVar_hsa_circ_30145,RMVar_hsa_circ_31263,RMVar_hsa_circ_4877,RMVar_hsa_circ_64170,RMVar_hsa_circ_62673 49136 RMVar_ID_49136 Human_SNP_ID_416366762 A-to-I Human chr9 + 130113404 130113404 130113404 ACAGGTCTTTCCACCATGCCCGGCTAATTCTTATATTTTTTGTAGAGACGGGGTCTCAATTTGTT ACAGGTCTTTCCACCATGCCCGGCTAATTCTTCTATTTTTTGTAGAGACGGGGTCTCAATTTGTT A C GPR107 Ensembl:ENSG00000148358 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1034690210 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_326380,RMVar_hsa_circ_316315,RMVar_hsa_circ_260300,RMVar_hsa_circ_377767,RMVar_hsa_circ_260301,RMVar_hsa_circ_30145,RMVar_hsa_circ_31263,RMVar_hsa_circ_4877,RMVar_hsa_circ_64170,RMVar_hsa_circ_62673 49137 RMVar_ID_49137 Human_SNP_ID_416367045 A-to-I Human chr9 + 130114457 130114457 130114457 CAGGCTGGAGTGCAGTGGTGTGATCATAGTTCATTGTAACCTCAAACTCCTAGGCTCATGTGATC CAGGCTGGAGTGCAGTGGTGTGATCATAGTTCGTTGTAACCTCAAACTCCTAGGCTCATGTGATC A G GPR107 Ensembl:ENSG00000148358 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs562261708 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_326380,RMVar_hsa_circ_316315,RMVar_hsa_circ_260300,RMVar_hsa_circ_377767,RMVar_hsa_circ_260301,RMVar_hsa_circ_30145,RMVar_hsa_circ_31263,RMVar_hsa_circ_4877,RMVar_hsa_circ_64170,RMVar_hsa_circ_62673 49138 RMVar_ID_49138 Human_SNP_ID_416369113 A-to-I Human chr9 + 130122894 130122894 130122894 GTGGTGGCACACACCTGTGGTCCCAGCTACTCAGGAGGCTGAGGATCACTTGAGTCTGGGAGGTC GTGGTGGCACACACCTGTGGTCCCAGCTACTCGGGAGGCTGAGGATCACTTGAGTCTGGGAGGTC A G GPR107 Ensembl:ENSG00000148358 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs776635145 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_326380,RMVar_hsa_circ_316315,RMVar_hsa_circ_260300,RMVar_hsa_circ_377767,RMVar_hsa_circ_260301,RMVar_hsa_circ_30145,RMVar_hsa_circ_31263,RMVar_hsa_circ_4877,RMVar_hsa_circ_64170,RMVar_hsa_circ_62673 49139 RMVar_ID_49139 Human_SNP_ID_416389208 A-to-I Human chr9 + 130196529 130196529 130196529 GGGAGGCCGAGGCGGATGGAACACTTGAGGTCAGGAGTTCGGGACCAGCCTGGCCAGCATGGTGA GGGAGGCCGAGGCGGATGGAACACTTGAGGTCGGGAGTTCGGGACCAGCCTGGCCAGCATGGTGA A G NCS1 Ensembl:ENSG00000107130 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs527556783 Functional Loss SNV dbSNP153 33..33 33 - - - 49140 RMVar_ID_49140 Human_SNP_ID_416391321 A-to-I Human chr9 + 130204494 130204494 130204494 AAAAAATTTTACTGTAGAGCTGGGGCCTCACTATATTGCCCAAGCTTGAGCTTCTGGCCTCAAGC AAAAAATTTTACTGTAGAGCTGGGGCCTCACTGTATTGCCCAAGCTTGAGCTTCTGGCCTCAAGC A G NCS1 Ensembl:ENSG00000107130 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1294442013 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83629,RMVar_hsa_circ_106542,RMVar_hsa_circ_260308,RMVar_hsa_circ_260309 49141 RMVar_ID_49141 Human_SNP_ID_416456229 A-to-I Human chr9 + 130448587 130448586 130448588 GGCTCACTGGTTTCTTTTGGTTTATTTAAGACAGAGTTTCACTCTGTCACCCAGGCTGGAGTGTG GGCTCACTGGTTTCTTTTGGTTTATTTAAGAC__AGTTTCACTCTGTCACCCAGGCTGGAGTGTG CAG C ASS1 Ensembl:ENSG00000130707 Protein coding intron GSE99789 esophageal squamous carcinoma cells,EC109 - 29796672 RNA-Seq:(High) rs1277798218 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_16592183 RMVar_hsa_circ_85141,RMVar_hsa_circ_102777,RMVar_hsa_circ_260316,RMVar_hsa_circ_260317 49142 RMVar_ID_49142 Human_SNP_ID_416492454 A-to-I Human chr9 + 130586501 130586501 130586501 TCAGCTCACTGCAACCTCTGCTTCTCGGGCTCAAGCAATCCTCCTTCCTCAGCCTCCCCAGTAGC TCAGCTCACTGCAACCTCTGCTTCTCGGGCTCGAGCAATCCTCCTTCCTCAGCCTCCCCAGTAGC A G FUBP3 Ensembl:ENSG00000107164 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs892157202 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87967,RMVar_hsa_circ_260335 49143 RMVar_ID_49143 Human_SNP_ID_416492744 A-to-I Human chr9 + 130587265 130587265 130587265 TTTTGTATTTTCTGTAGAGATGCGGTTTCACCATGTTGGCCATGATGGTCTCAATCTCCTGACCT TTTTGTATTTTCTGTAGAGATGCGGTTTCACCGTGTTGGCCATGATGGTCTCAATCTCCTGACCT A G FUBP3 Ensembl:ENSG00000107164 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1002154718 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26207554 RMVar_hsa_circ_87967,RMVar_hsa_circ_260335 49144 RMVar_ID_49144 Human_SNP_ID_416494343 A-to-I Human chr9 + 130592643 130592643 130592643 TCGTAGCTCACTGTAACCTCAAACCCCGGCTCAAGCAGTCCTCCTGCCTCAGCCTCCTGAGTAGC TCGTAGCTCACTGTAACCTCAAACCCCGGCTCGAGCAGTCCTCCTGCCTCAGCCTCCTGAGTAGC A G FUBP3 Ensembl:ENSG00000107164 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1015585748 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16592973 RMVar_hsa_circ_87967,RMVar_hsa_circ_260335 49145 RMVar_ID_49145 Human_SNP_ID_416494345 A-to-I Human chr9 + 130592647 130592647 130592647 AGCTCACTGTAACCTCAAACCCCGGCTCAAGCAGTCCTCCTGCCTCAGCCTCCTGAGTAGCCGGG AGCTCACTGTAACCTCAAACCCCGGCTCAAGCGGTCCTCCTGCCTCAGCCTCCTGAGTAGCCGGG A G FUBP3 Ensembl:ENSG00000107164 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs954787813 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87967,RMVar_hsa_circ_260335 49146 RMVar_ID_49146 Human_SNP_ID_416497497 A-to-I Human chr9 + 130604469 130604469 130604469 TGACAGATCAAGGTTTGAATCCCAGCTTTGCTAGTCATTAGCTGTTTGACCTTGGGCAAGTTCCT TGACAGATCAAGGTTTGAATCCCAGCTTTGCTGGTCATTAGCTGTTTGACCTTGGGCAAGTTCCT A G FUBP3 Ensembl:ENSG00000107164 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1299861128 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16593404 RMVar_hsa_circ_87967,RMVar_hsa_circ_104170,RMVar_hsa_circ_260335,RMVar_hsa_circ_74958,RMVar_hsa_circ_260337 49147 RMVar_ID_49147 Human_SNP_ID_416523794 A-to-I Human chr9 + 130699792 130699792 130699792 GGAAGGCCAAGGAGGGAGGACTGCTTGAGCCTAAGAGTTCAAGACCAGCCTGGGCAACATAGCAA GGAAGGCCAAGGAGGGAGGACTGCTTGAGCCTCAGAGTTCAAGACCAGCCTGGGCAACATAGCAA A C EXOSC2 Ensembl:ENSG00000130713 Protein coding intron GSE123020:GSM3490829,GSM3490830,GSM3490831 esophageal squamous carcinoma cells,EC109 cell line - 32596459 RNA-Seq:(High) rs555888381 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27697,RMVar_hsa_circ_118964,RMVar_hsa_circ_260348,RMVar_hsa_circ_91666,RMVar_hsa_circ_260347,RMVar_hsa_circ_123461,RMVar_hsa_circ_260350 49148 RMVar_ID_49148 Human_SNP_ID_416523832 A-to-I Human chr9 + 130699946 130699946 130699946 AGAGGGTTGCTTGAGCCCAGGAGCTCAAGGCTACAGTAAGCTATGATCACACCACTGCATTCCAG AGAGGGTTGCTTGAGCCCAGGAGCTCAAGGCTGCAGTAAGCTATGATCACACCACTGCATTCCAG A G EXOSC2 Ensembl:ENSG00000130713 Protein coding intron GSE100210;GSE99789 HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 29129909,29796672 RNA-Seq:(High) rs1011803939 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27697,RMVar_hsa_circ_118964,RMVar_hsa_circ_260348,RMVar_hsa_circ_91666,RMVar_hsa_circ_260347,RMVar_hsa_circ_123461,RMVar_hsa_circ_260350 49149 RMVar_ID_49149 Human_SNP_ID_416523835 A-to-I Human chr9 + 130699951 130699951 130699951 GTTGCTTGAGCCCAGGAGCTCAAGGCTACAGTAAGCTATGATCACACCACTGCATTCCAGCTTGG GTTGCTTGAGCCCAGGAGCTCAAGGCTACAGTGAGCTATGATCACACCACTGCATTCCAGCTTGG A G EXOSC2 Ensembl:ENSG00000130713 Protein coding intron GSE38233;GSE100210;GSE99789;GSE99789 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109 - 24183664,29129909,29796672,29796672 RNA-Seq:(High) rs900792124 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27697,RMVar_hsa_circ_118964,RMVar_hsa_circ_260348,RMVar_hsa_circ_91666,RMVar_hsa_circ_260347,RMVar_hsa_circ_123461,RMVar_hsa_circ_260350 49150 RMVar_ID_49150 Human_SNP_ID_416523841 A-to-I Human chr9 + 130699977 130699977 130699977 TACAGTAAGCTATGATCACACCACTGCATTCCAGCTTGGGTGACAGAACAAGACTCTGTCTCTAT TACAGTAAGCTATGATCACACCACTGCATTCCTGCTTGGGTGACAGAACAAGACTCTGTCTCTAT A T EXOSC2 Ensembl:ENSG00000130713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1424464425 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7903047 RMVar_hsa_circ_27697,RMVar_hsa_circ_118964,RMVar_hsa_circ_260348,RMVar_hsa_circ_91666,RMVar_hsa_circ_260347,RMVar_hsa_circ_123461,RMVar_hsa_circ_260350 49151 RMVar_ID_49151 Human_SNP_ID_416523878 A-to-I Human chr9 + 130700100 130700100 130700100 CAGACTGGAGTGCAGTGGCGCGATCTCGGCTCACTGCAACGTCCGCCTCTTGGATTCAAGCAATT CAGACTGGAGTGCAGTGGCGCGATCTCGGCTCGCTGCAACGTCCGCCTCTTGGATTCAAGCAATT A G EXOSC2 Ensembl:ENSG00000130713 Protein coding intron GSE38233;GSE100210;GSE99789;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,29796672,31158229 RNA-Seq:(High) rs900740109 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27697,RMVar_hsa_circ_118964,RMVar_hsa_circ_260348,RMVar_hsa_circ_91666,RMVar_hsa_circ_260347,RMVar_hsa_circ_123461,RMVar_hsa_circ_260350 49152 RMVar_ID_49152 Human_SNP_ID_416523879 A-to-I Human chr9 + 130700105 130700105 130700105 TGGAGTGCAGTGGCGCGATCTCGGCTCACTGCAACGTCCGCCTCTTGGATTCAAGCAATTCTGCC TGGAGTGCAGTGGCGCGATCTCGGCTCACTGCGACGTCCGCCTCTTGGATTCAAGCAATTCTGCC A G EXOSC2 Ensembl:ENSG00000130713 Protein coding intron GSE38233;GSE100210;GSE100210;GSE99789;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,29129909,29796672,31158229,32596459,32596459 RNA-Seq:(High) rs1268804308 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27697,RMVar_hsa_circ_118964,RMVar_hsa_circ_260348,RMVar_hsa_circ_91666,RMVar_hsa_circ_260347,RMVar_hsa_circ_123461,RMVar_hsa_circ_260350 49153 RMVar_ID_49153 Human_SNP_ID_416523889 A-to-I Human chr9 + 130700156 130700156 130700156 CAAGCAATTCTGCCTTAGCCTCCCAAATAGCTAGGATTACCGGCGTGCGTCATGCCTGGCTAATT CAAGCAATTCTGCCTTAGCCTCCCAAATAGCTGGGATTACCGGCGTGCGTCATGCCTGGCTAATT A G EXOSC2 Ensembl:ENSG00000130713 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1477457481 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7903055 RMVar_hsa_circ_27697,RMVar_hsa_circ_118964,RMVar_hsa_circ_260348,RMVar_hsa_circ_91666,RMVar_hsa_circ_260347,RMVar_hsa_circ_123461,RMVar_hsa_circ_260350 49154 RMVar_ID_49154 Human_SNP_ID_416524995 A-to-I Human chr9 + 130704272 130704272 130704272 ACCAAGCAGGCCAGGCACGGTGGCTCACGCCTATAATCCCAGCACTTAGGGAGGCCAAGGCGGGC ACCAAGCAGGCCAGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTAGGGAGGCCAAGGCGGGC A G EXOSC2 Ensembl:ENSG00000130713 Protein coding 3'UTR GSE38233;GSE100210;GSE99789 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 24183664,29129909,29796672 RNA-Seq:(High) rs1276195582 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26565443 Human_miRNA_ID_2315728,Human_miRNA_ID_2318884,Human_miRNA_ID_2322045,Human_miRNA_ID_2325211,Human_miRNA_ID_2328330,Human_miRNA_ID_2519588,Human_miRNA_ID_2522753,Human_miRNA_ID_2774594,Human_miRNA_ID_2821947,Human_miRNA_ID_2828077,Human_miRNA_ID_2831233,Human_miRNA_ID_2835353,Human_miRNA_ID_2840709 RMVar_hsa_circ_91666,RMVar_hsa_circ_260347,RMVar_hsa_circ_123461,RMVar_hsa_circ_260350 49155 RMVar_ID_49155 Human_SNP_ID_416525003 A-to-I Human chr9 + 130704287 130704287 130704287 CACGGTGGCTCACGCCTATAATCCCAGCACTTAGGGAGGCCAAGGCGGGCAGATCACCTGAGGTC CACGGTGGCTCACGCCTATAATCCCAGCACTTGGGGAGGCCAAGGCGGGCAGATCACCTGAGGTC A G EXOSC2 Ensembl:ENSG00000130713 Protein coding 3'UTR GSE38233;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line - 24183664,29796672,31158229 RNA-Seq:(High) rs929340455 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23090475 Human_miRNA_ID_2217753,Human_miRNA_ID_2315728,Human_miRNA_ID_2318884,Human_miRNA_ID_2322045,Human_miRNA_ID_2325211,Human_miRNA_ID_2328330,Human_miRNA_ID_2519588,Human_miRNA_ID_2522753,Human_miRNA_ID_2821947,Human_miRNA_ID_2828077,Human_miRNA_ID_2831233,Human_miRNA_ID_2835353,Human_miRNA_ID_2840709 RMVar_hsa_circ_91666,RMVar_hsa_circ_260347,RMVar_hsa_circ_123461,RMVar_hsa_circ_260350 49156 RMVar_ID_49156 Human_SNP_ID_416525015 A-to-I Human chr9 + 130704343 130704341 130704344 CCTGAGGTCAATAGTTCGAGACCAGCCTGGCCAACAAGGTGAAACCCCATCTCTACTAAAAATAC CCTGAGGTCAATAGTTCGAGACCAGCCTGGC___CAAGGTGAAACCCCATCTCTACTAAAAATAC CCAA C EXOSC2 Ensembl:ENSG00000130713 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1186731330 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_16594784 RMVar_hsa_circ_91666,RMVar_hsa_circ_260347,RMVar_hsa_circ_123461,RMVar_hsa_circ_260350 49157 RMVar_ID_49157 Human_SNP_ID_416525026 A-to-I Human chr9 + 130704410 130704410 130704410 AAAATTAGCCAGGTGTGGTGGTGTGCACCTGTAGTCCCAGCTATTTGGGAGGCTGAGGTGGGAGA AAAATTAGCCAGGTGTGGTGGTGTGCACCTGTGGTCCCAGCTATTTGGGAGGCTGAGGTGGGAGA A G EXOSC2 Ensembl:ENSG00000130713 Protein coding 3'UTR GSE38233;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29796672,31158229,31158229 RNA-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 49158 RMVar_ID_49158 Human_SNP_ID_416525039 A-to-I Human chr9 + 130704472 130704472 130704472 AGAATCACTTGAACCTGGGAGGCGGAGGTTGCAGTGAGCTGAAATCGCGTACCACACTCCAGCCT AGAATCACTTGAACCTGGGAGGCGGAGGTTGCTGTGAGCTGAAATCGCGTACCACACTCCAGCCT A T EXOSC2 Ensembl:ENSG00000130713 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1445593318 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26566134 RMVar_hsa_circ_91666,RMVar_hsa_circ_260347,RMVar_hsa_circ_123461,RMVar_hsa_circ_260350 49159 RMVar_ID_49159 Human_SNP_ID_416525169 A-to-I Human chr9 + 130705018 130705018 130705018 TGAGTGGGCAGATCACCTGAGGTCAGGAGTTCAAGACCAGCCCGGCCAATACAGTGAAACCTCGT TGAGTGGGCAGATCACCTGAGGTCAGGAGTTCCAGACCAGCCCGGCCAATACAGTGAAACCTCGT A C - - Other Unknown GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-Seq:(High) rs1042678904 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23200468 RMVar_hsa_circ_91666,RMVar_hsa_circ_260347,RMVar_hsa_circ_123461,RMVar_hsa_circ_260350 49160 RMVar_ID_49160 Human_SNP_ID_416525212 A-to-I Human chr9 + 130705178 130705178 130705178 CGGGAGGCGGAGTTGCAGTGAGCTGAGATCGCACCATTGCACTTCAGCCTAGGTGACACAGTGAG CGGGAGGCGGAGTTGCAGTGAGCTGAGATCGCGCCATTGCACTTCAGCCTAGGTGACACAGTGAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1189118536 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16594822,Human_RBP_ID_26241898 49161 RMVar_ID_49161 Human_SNP_ID_416525218 A-to-I Human chr9 + 130705196 130705196 130705196 TGAGCTGAGATCGCACCATTGCACTTCAGCCTAGGTGACACAGTGAGACTGTCTCGAAAGAAAGG TGAGCTGAGATCGCACCATTGCACTTCAGCCTGGGTGACACAGTGAGACTGTCTCGAAAGAAAGG A G - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1358371854 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7903148,Human_RBP_ID_16594822,Human_RBP_ID_23200470 49162 RMVar_ID_49162 Human_SNP_ID_416525264 A-to-I Human chr9 + 130705305 130705305 130705305 AGCACTTTGGGAGGCTGAGGTGGGTGGATCACAAGGTCAGATCGAGACCATCCTGGCTAACATGG AGCACTTTGGGAGGCTGAGGTGGGTGGATCACGAGGTCAGATCGAGACCATCCTGGCTAACATGG A G - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs923776533 Functional Loss SNV dbSNP153 33..33 33 - - - 49163 RMVar_ID_49163 Human_SNP_ID_416525427 A-to-I Human chr9 + 130705737 130705737 130705737 AGCTGGGACTATAGGCATGCGCCAACACGCCCAGCTAATTTTTGTGTTTTTAGTGGAGATCGTTT AGCTGGGACTATAGGCATGCGCCAACACGCCCGGCTAATTTTTGTGTTTTTAGTGGAGATCGTTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1361574222 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16594832,Human_RBP_ID_26561700 49164 RMVar_ID_49164 Human_SNP_ID_416525436 A-to-I Human chr9 + 130705774 130705774 130705774 ATTTTTGTGTTTTTAGTGGAGATCGTTTCACCATGTTGAGCAGGCTGGTCTCGATCTCTTGACCT ATTTTTGTGTTTTTAGTGGAGATCGTTTCACCTTGTTGAGCAGGCTGGTCTCGATCTCTTGACCT A T - - Other Unknown GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1194844309 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1058250,Human_RBP_ID_18396513,Human_RBP_ID_26561701 49165 RMVar_ID_49165 Human_SNP_ID_416525457 A-to-I Human chr9 + 130705846 130705846 130705846 CACCCGCCTCGGCCTCCCAAAGTGTTTGGATTACAGGTATGAACCACTGCACCCAGCCATATTTT CACCCGCCTCGGCCTCCCAAAGTGTTTGGATTGCAGGTATGAACCACTGCACCCAGCCATATTTT A G - - Other Unknown GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1450159475 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16594837,Human_RBP_ID_23200475 49166 RMVar_ID_49166 Human_SNP_ID_416525566 A-to-I Human chr9 + 130706078 130706077 130706078 TGCCACCACGCCCAACTAATTTTTGTATTTTTAGTAGAGGTGGCATTCTACCATGTTGGCCAGGA TGCCACCACGCCCAACTAATTTTTGTATTTTT_GTAGAGGTGGCATTCTACCATGTTGGCCAGGA TA T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1220478023 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_16594845,Human_RBP_ID_23200479 49167 RMVar_ID_49167 Human_SNP_ID_416525570 A-to-I Human chr9 + 130706107 130706107 130706107 TTTAGTAGAGGTGGCATTCTACCATGTTGGCCAGGATGGTTTTGATTTCCTGACCTTGTGATCCC TTTAGTAGAGGTGGCATTCTACCATGTTGGCCCGGATGGTTTTGATTTCCTGACCTTGTGATCCC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs914761077 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16594846,Human_RBP_ID_26561703,Human_RBP_ID_27543067 49168 RMVar_ID_49168 Human_SNP_ID_416525571 A-to-I Human chr9 + 130706107 130706107 130706107 TTTAGTAGAGGTGGCATTCTACCATGTTGGCCAGGATGGTTTTGATTTCCTGACCTTGTGATCCC TTTAGTAGAGGTGGCATTCTACCATGTTGGCCGGGATGGTTTTGATTTCCTGACCTTGTGATCCC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs914761077 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16594846,Human_RBP_ID_26561703,Human_RBP_ID_27543067 49169 RMVar_ID_49169 Human_SNP_ID_416525583 A-to-I Human chr9 + 130706157 130706157 130706157 TGACCTTGTGATCCCCCCGCCTCAGCCTGCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGAGC TGACCTTGTGATCCCCCCGCCTCAGCCTGCCAGAGTGCTGGGATTACAGGCGTGAGCCACTGAGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1208384112 Functional Loss SNV dbSNP153 33..33 33 - - - 49170 RMVar_ID_49170 Human_SNP_ID_416525663 A-to-I Human chr9 + 130706472 130706468 130706472 TACCTCACTTTCTTTTTTTGAGACAGGGTCTCACTCTGTCACCCAGGCTGGAGTGGGGTGGCATG TACCTCACTTTCTTTTTTTGAGACAGGGT____CTCTGTCACCCAGGCTGGAGTGGGGTGGCATG TCTCA T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935547991 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_26561712 49171 RMVar_ID_49171 Human_SNP_ID_416525753 A-to-I Human chr9 + 130706811 130706811 130706811 TTTTTGTTTTTCGGCAGAGATGAAGTCTCACTATGTTGCCCAGGCTGGTCTTGAACTCCTGACCT TTTTTGTTTTTCGGCAGAGATGAAGTCTCACTGTGTTGCCCAGGCTGGTCTTGAACTCCTGACCT A G - - Other Unknown GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs920672471 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7903171,Human_RBP_ID_16594903,Human_RBP_ID_27543070 49172 RMVar_ID_49172 Human_SNP_ID_416526032 A-to-I Human chr9 + 130707827 130707827 130707827 ACTGCAACCTCCGCCTCCCGGGTTCACGTGATACTCTTGCCTCAGCTTCCTGCATAGCTGGGACT ACTGCAACCTCCGCCTCCCGGGTTCACGTGATGCTCTTGCCTCAGCTTCCTGCATAGCTGGGACT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs548151355 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7903202,Human_RBP_ID_16594955 49173 RMVar_ID_49173 Human_SNP_ID_416526111 A-to-I Human chr9 + 130708080 130708080 130708080 GCCACCATGCCCAGCTAATTTTGTGTATGTTTAGTAGAGACGAGGTTTCACTGTGTTAACCAGGA GCCACCATGCCCAGCTAATTTTGTGTATGTTTCGTAGAGACGAGGTTTCACTGTGTTAACCAGGA A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1358476191 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_713667,Human_RBP_ID_16594961 49174 RMVar_ID_49174 Human_SNP_ID_416526118 A-to-I Human chr9 + 130708105 130708105 130708105 TATGTTTAGTAGAGACGAGGTTTCACTGTGTTAACCAGGATGGTCTCTATCTTCTGACCTCGTGA TATGTTTAGTAGAGACGAGGTTTCACTGTGTTGACCAGGATGGTCTCTATCTTCTGACCTCGTGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1390928547 Functional Loss SNV dbSNP153 33..33 33 - - - 49175 RMVar_ID_49175 Human_SNP_ID_416526165 A-to-I Human chr9 + 130708308 130708308 130708308 TGCCTGCCTTGGCCTCCTGAAGTGTTGGGATTACAGGTGTGAGCCACCACACCCAGCCAAGCAAT TGCCTGCCTTGGCCTCCTGAAGTGTTGGGATTGCAGGTGTGAGCCACCACACCCAGCCAAGCAAT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1056730219 Functional Loss SNV dbSNP153 33..33 33 - - - 49176 RMVar_ID_49176 Human_SNP_ID_416526263 A-to-I Human chr9 + 130708678 130708678 130708678 CTGGGCGTGGTGGTGGGTGCCTGTAATCCCTCAGGAGGCTGAGGCAGGTGAATCGCTTGAACCCG CTGGGCGTGGTGGTGGGTGCCTGTAATCCCTCTGGAGGCTGAGGCAGGTGAATCGCTTGAACCCG A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1320540723 Functional Loss SNV dbSNP153 33..33 33 - - - 49177 RMVar_ID_49177 Human_SNP_ID_416526276 A-to-I Human chr9 + 130708726 130708726 130708726 TGAATCGCTTGAACCCGGGAGGTGGAGGTTGCAATGATCCGGGATCGTGCCACTGCACTCCAGCC TGAATCGCTTGAACCCGGGAGGTGGAGGTTGCCATGATCCGGGATCGTGCCACTGCACTCCAGCC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992296221 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22517875 49178 RMVar_ID_49178 Human_SNP_ID_416526277 A-to-I Human chr9 + 130708726 130708726 130708726 TGAATCGCTTGAACCCGGGAGGTGGAGGTTGCAATGATCCGGGATCGTGCCACTGCACTCCAGCC TGAATCGCTTGAACCCGGGAGGTGGAGGTTGCGATGATCCGGGATCGTGCCACTGCACTCCAGCC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992296221 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22517875 49179 RMVar_ID_49179 Human_SNP_ID_416526278 A-to-I Human chr9 + 130708726 130708726 130708726 TGAATCGCTTGAACCCGGGAGGTGGAGGTTGCAATGATCCGGGATCGTGCCACTGCACTCCAGCC TGAATCGCTTGAACCCGGGAGGTGGAGGTTGCTATGATCCGGGATCGTGCCACTGCACTCCAGCC A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992296221 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22517875 49180 RMVar_ID_49180 Human_SNP_ID_416526290 A-to-I Human chr9 + 130708750 130708750 130708750 GAGGTTGCAATGATCCGGGATCGTGCCACTGCACTCCAGCCGGGGTGACAGAGTGAGACTCTGTC GAGGTTGCAATGATCCGGGATCGTGCCACTGCCCTCCAGCCGGGGTGACAGAGTGAGACTCTGTC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1364789310 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22517875,Human_RBP_ID_23200522 49181 RMVar_ID_49181 Human_SNP_ID_416529894 A-to-I Human chr9 + 130721255 130721255 130721255 ACAAAAATTAGTCGGCATGGTGGCACACACCTATAGTCCCACCTACATGGGAGGCTGAGGCAGAG ACAAAAATTAGTCGGCATGGTGGCACACACCTGTAGTCCCACCTACATGGGAGGCTGAGGCAGAG A G ABL1 Ensembl:ENSG00000097007 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1205008187 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_260352,RMVar_hsa_circ_110781,RMVar_hsa_circ_76537,RMVar_hsa_circ_260351 49182 RMVar_ID_49182 Human_SNP_ID_416531624 A-to-I Human chr9 + 130727615 130727615 130727615 AAACCCTGTCTCTTACTAAAAATACAAAAATTAGCTGGGCTTGGTGGCAGCTGCCTATAGCTACT AAACCCTGTCTCTTACTAAAAATACAAAAATTGGCTGGGCTTGGTGGCAGCTGCCTATAGCTACT A G ABL1 Ensembl:ENSG00000097007 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1247229961 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_260352,RMVar_hsa_circ_110781,RMVar_hsa_circ_76537,RMVar_hsa_circ_260351 49183 RMVar_ID_49183 Human_SNP_ID_416531818 A-to-I Human chr9 + 130728157 130728157 130728157 GCAATCATAGCTCACTGCAACCTCCGTCTCCCAGACTCAAGCTGTTCTCCCACCTCAGCCTCCTG GCAATCATAGCTCACTGCAACCTCCGTCTCCCGGACTCAAGCTGTTCTCCCACCTCAGCCTCCTG A G ABL1 Ensembl:ENSG00000097007 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs914313846 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_260352,RMVar_hsa_circ_110781,RMVar_hsa_circ_76537,RMVar_hsa_circ_260351 49184 RMVar_ID_49184 Human_SNP_ID_416539793 A-to-I Human chr9 + 130757283 130757283 130757283 TCCTGTTTTCCTATTGAAAACTGAAATTGGCCAGCCACAGTGGCTCATGTCTGTAATCCCAGCCC TCCTGTTTTCCTATTGAAAACTGAAATTGGCCGGCCACAGTGGCTCATGTCTGTAATCCCAGCCC A G ABL1 Ensembl:ENSG00000097007 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs891064558 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_260352,RMVar_hsa_circ_110781,RMVar_hsa_circ_76537,RMVar_hsa_circ_260351 49185 RMVar_ID_49185 Human_SNP_ID_416542529 A-to-I Human chr9 + 130767407 130767407 130767407 TCCAGGCTGGACTGCAGTGACAATCTCTGCTCACTATAACCTCCGCCTCCCGGGTTCAAGCGATT TCCAGGCTGGACTGCAGTGACAATCTCTGCTCTCTATAACCTCCGCCTCCCGGGTTCAAGCGATT A T ABL1 Ensembl:ENSG00000097007 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1489750575 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_260352,RMVar_hsa_circ_110781,RMVar_hsa_circ_76537,RMVar_hsa_circ_260351 49186 RMVar_ID_49186 Human_SNP_ID_416550801 A-to-I Human chr9 + 130803274 130803274 130803274 GTTGGCCAGGCTGGTCACGAACTCGTGAACTCATGCTCTACCCGCCTCAGCCTCCCCAAGTGCTG GTTGGCCAGGCTGGTCACGAACTCGTGAACTCGTGCTCTACCCGCCTCAGCCTCCCCAAGTGCTG A G ABL1 Ensembl:ENSG00000097007 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1302840673 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_260352,RMVar_hsa_circ_110781,RMVar_hsa_circ_76537,RMVar_hsa_circ_260351 49187 RMVar_ID_49187 Human_SNP_ID_416550805 A-to-I Human chr9 + 130803281 130803281 130803281 AGGCTGGTCACGAACTCGTGAACTCATGCTCTACCCGCCTCAGCCTCCCCAAGTGCTGGGATTAC AGGCTGGTCACGAACTCGTGAACTCATGCTCTCCCCGCCTCAGCCTCCCCAAGTGCTGGGATTAC A C ABL1 Ensembl:ENSG00000097007 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1044229161 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_260352,RMVar_hsa_circ_110781,RMVar_hsa_circ_76537,RMVar_hsa_circ_260351 49188 RMVar_ID_49188 Human_SNP_ID_416553160 A-to-I Human chr9 + 130812300 130812300 130812300 GGAGGATCACTTGAGCCCAGGAGTTTGAGGCTACAGTGAGCTCTGATCACACCACTGCACTCCTC GGAGGATCACTTGAGCCCAGGAGTTTGAGGCTGCAGTGAGCTCTGATCACACCACTGCACTCCTC A G ABL1 Ensembl:ENSG00000097007 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1192985027 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_260352,RMVar_hsa_circ_110781,RMVar_hsa_circ_76537,RMVar_hsa_circ_260351 49189 RMVar_ID_49189 Human_SNP_ID_416557155 A-to-I Human chr9 + 130829305 130829305 130829305 AACTGAGCCCGGGCACGGTGGCTCACACCTGTAATCGCAGCACTTTGGGAGGCCGAGGCGGGCAG AACTGAGCCCGGGCACGGTGGCTCACACCTGTGATCGCAGCACTTTGGGAGGCCGAGGCGGGCAG A G ABL1 Ensembl:ENSG00000097007 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1292706404 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_260352,RMVar_hsa_circ_110781,RMVar_hsa_circ_76537,RMVar_hsa_circ_260351 49190 RMVar_ID_49190 Human_SNP_ID_416619922 A-to-I Human chr9 + 131048156 131048156 131048156 TCAGCTCGCTGCAACCTCCGCCTCTCGGGTTCAGGCGATTCTCCTGCCTCAGCCTCCTGAGTAGC TCAGCTCGCTGCAACCTCCGCCTCTCGGGTTCCGGCGATTCTCCTGCCTCAGCCTCCTGAGTAGC A C LAMC3 Ensembl:ENSG00000050555 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935577785 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88082,RMVar_hsa_circ_260367 49191 RMVar_ID_49191 Human_SNP_ID_416619923 A-to-I Human chr9 + 131048156 131048156 131048156 TCAGCTCGCTGCAACCTCCGCCTCTCGGGTTCAGGCGATTCTCCTGCCTCAGCCTCCTGAGTAGC TCAGCTCGCTGCAACCTCCGCCTCTCGGGTTCGGGCGATTCTCCTGCCTCAGCCTCCTGAGTAGC A G LAMC3 Ensembl:ENSG00000050555 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935577785 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88082,RMVar_hsa_circ_260367 49192 RMVar_ID_49192 Human_SNP_ID_416660100 A-to-I Human chr9 + 131195902 131195902 131195902 ACAAAATTAGCCAGCCGTGGTGGCGCATACCTATAATCCCAGCTACTCAGGAGGCTGAGGCAGGA ACAAAATTAGCCAGCCGTGGTGGCGCATACCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGA A G NUP214 Ensembl:ENSG00000126883 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs537099085 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83409,RMVar_hsa_circ_260379,RMVar_hsa_circ_53094,RMVar_hsa_circ_86474,RMVar_hsa_circ_260389,RMVar_hsa_circ_33833,RMVar_hsa_circ_87476,RMVar_hsa_circ_59170,RMVar_hsa_circ_109692,RMVar_hsa_circ_260396,RMVar_hsa_circ_343264,RMVar_hsa_circ_364906,RMVar_hsa_circ_290858,RMVar_hsa_circ_111390,RMVar_hsa_circ_260404,RMVar_hsa_circ_260406,RMVar_hsa_circ_100251,RMVar_hsa_circ_260405,RMVar_hsa_circ_260412,RMVar_hsa_circ_123184,RMVar_hsa_circ_50584,RMVar_hsa_circ_342436,RMVar_hsa_circ_301956,RMVar_hsa_circ_260414 49193 RMVar_ID_49193 Human_SNP_ID_416660101 A-to-I Human chr9 + 131195902 131195902 131195902 ACAAAATTAGCCAGCCGTGGTGGCGCATACCTATAATCCCAGCTACTCAGGAGGCTGAGGCAGGA ACAAAATTAGCCAGCCGTGGTGGCGCATACCTTTAATCCCAGCTACTCAGGAGGCTGAGGCAGGA A T NUP214 Ensembl:ENSG00000126883 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs537099085 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83409,RMVar_hsa_circ_260379,RMVar_hsa_circ_53094,RMVar_hsa_circ_86474,RMVar_hsa_circ_260389,RMVar_hsa_circ_33833,RMVar_hsa_circ_87476,RMVar_hsa_circ_59170,RMVar_hsa_circ_109692,RMVar_hsa_circ_260396,RMVar_hsa_circ_343264,RMVar_hsa_circ_364906,RMVar_hsa_circ_290858,RMVar_hsa_circ_111390,RMVar_hsa_circ_260404,RMVar_hsa_circ_260406,RMVar_hsa_circ_100251,RMVar_hsa_circ_260405,RMVar_hsa_circ_260412,RMVar_hsa_circ_123184,RMVar_hsa_circ_50584,RMVar_hsa_circ_342436,RMVar_hsa_circ_301956,RMVar_hsa_circ_260414 49194 RMVar_ID_49194 Human_SNP_ID_416660106 A-to-I Human chr9 + 131195914 131195914 131195914 AGCCGTGGTGGCGCATACCTATAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAA AGCCGTGGTGGCGCATACCTATAATCCCAGCTTCTCAGGAGGCTGAGGCAGGAGAATTGCTTGAA A T NUP214 Ensembl:ENSG00000126883 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs555822670 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83409,RMVar_hsa_circ_260379,RMVar_hsa_circ_53094,RMVar_hsa_circ_86474,RMVar_hsa_circ_260389,RMVar_hsa_circ_33833,RMVar_hsa_circ_87476,RMVar_hsa_circ_59170,RMVar_hsa_circ_109692,RMVar_hsa_circ_260396,RMVar_hsa_circ_343264,RMVar_hsa_circ_364906,RMVar_hsa_circ_290858,RMVar_hsa_circ_111390,RMVar_hsa_circ_260404,RMVar_hsa_circ_260406,RMVar_hsa_circ_100251,RMVar_hsa_circ_260405,RMVar_hsa_circ_260412,RMVar_hsa_circ_123184,RMVar_hsa_circ_50584,RMVar_hsa_circ_342436,RMVar_hsa_circ_301956,RMVar_hsa_circ_260414 49195 RMVar_ID_49195 Human_SNP_ID_416663631 A-to-I Human chr9 + 131208756 131208756 131208756 AATGAAGTTCTCGGCTGGGCATGGTGGCTCACACCTTTAATCCCAGCACTTTGGGAGGCTGAGGC AATGAAGTTCTCGGCTGGGCATGGTGGCTCACGCCTTTAATCCCAGCACTTTGGGAGGCTGAGGC A G NUP214 Ensembl:ENSG00000126883 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1423306790 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_53094,RMVar_hsa_circ_86474,RMVar_hsa_circ_260389,RMVar_hsa_circ_87476,RMVar_hsa_circ_59170,RMVar_hsa_circ_109692,RMVar_hsa_circ_260396,RMVar_hsa_circ_111390,RMVar_hsa_circ_260404,RMVar_hsa_circ_260406,RMVar_hsa_circ_100251,RMVar_hsa_circ_260405,RMVar_hsa_circ_260412,RMVar_hsa_circ_123184,RMVar_hsa_circ_50584,RMVar_hsa_circ_26267,RMVar_hsa_circ_351188,RMVar_hsa_circ_268435,RMVar_hsa_circ_125812,RMVar_hsa_circ_327564,RMVar_hsa_circ_293005,RMVar_hsa_circ_260416,RMVar_hsa_circ_260417 49196 RMVar_ID_49196 Human_SNP_ID_416664062 A-to-I Human chr9 + 131210446 131210446 131210446 GGTCAGGAGTTCAAGACCAGCCTGGCCAACATAGTGAAACCCCATCTCTACTAAAAATACTAAAA GGTCAGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACTAAAA A G NUP214 Ensembl:ENSG00000126883 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1564212633 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_53094,RMVar_hsa_circ_86474,RMVar_hsa_circ_260389,RMVar_hsa_circ_87476,RMVar_hsa_circ_59170,RMVar_hsa_circ_109692,RMVar_hsa_circ_260396,RMVar_hsa_circ_111390,RMVar_hsa_circ_260404,RMVar_hsa_circ_260406,RMVar_hsa_circ_100251,RMVar_hsa_circ_260405,RMVar_hsa_circ_260412,RMVar_hsa_circ_123184,RMVar_hsa_circ_50584,RMVar_hsa_circ_26267,RMVar_hsa_circ_351188,RMVar_hsa_circ_268435,RMVar_hsa_circ_125812,RMVar_hsa_circ_327564,RMVar_hsa_circ_293005,RMVar_hsa_circ_260416,RMVar_hsa_circ_260417 49197 RMVar_ID_49197 Human_SNP_ID_416664075 A-to-I Human chr9 + 131210488 131210488 131210488 CATCTCTACTAAAAATACTAAAATTAGCCGGCATGGTGGCGCGCCCCTGTAGTCCCAGCTACTCG CATCTCTACTAAAAATACTAAAATTAGCCGGCCTGGTGGCGCGCCCCTGTAGTCCCAGCTACTCG A C NUP214 Ensembl:ENSG00000126883 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs540958599 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_53094,RMVar_hsa_circ_86474,RMVar_hsa_circ_260389,RMVar_hsa_circ_87476,RMVar_hsa_circ_59170,RMVar_hsa_circ_109692,RMVar_hsa_circ_260396,RMVar_hsa_circ_111390,RMVar_hsa_circ_260404,RMVar_hsa_circ_260406,RMVar_hsa_circ_100251,RMVar_hsa_circ_260405,RMVar_hsa_circ_260412,RMVar_hsa_circ_123184,RMVar_hsa_circ_50584,RMVar_hsa_circ_26267,RMVar_hsa_circ_351188,RMVar_hsa_circ_268435,RMVar_hsa_circ_125812,RMVar_hsa_circ_327564,RMVar_hsa_circ_293005,RMVar_hsa_circ_260416,RMVar_hsa_circ_260417 49198 RMVar_ID_49198 Human_SNP_ID_416669301 A-to-I Human chr9 + 131230974 131230974 131230974 CTTGAGCCCAGGAGTTTGAGACTAGCCTGGGCAACATGGCAAGACTCCATTCTCTACAAAAAATG CTTGAGCCCAGGAGTTTGAGACTAGCCTGGGCGACATGGCAAGACTCCATTCTCTACAAAAAATG A G NUP214 Ensembl:ENSG00000126883 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs878962502 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86474,RMVar_hsa_circ_260389,RMVar_hsa_circ_87476,RMVar_hsa_circ_260396,RMVar_hsa_circ_111390,RMVar_hsa_circ_260404,RMVar_hsa_circ_260412,RMVar_hsa_circ_123184,RMVar_hsa_circ_83598,RMVar_hsa_circ_260418 49199 RMVar_ID_49199 Human_SNP_ID_416715500 A-to-I Human chr9 + 131399025 131399025 131399025 AGGTCGGGCACGGTGGCTCACGCCTGTAATCCAAGCACTTTGGCAGGCCGAGGTGGGCGGATCAC AGGTCGGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGCAGGCCGAGGTGGGCGGATCAC A C PRRC2B Ensembl:ENSG00000130723 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1192108960 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16598859,Human_RBP_ID_23200560 RMVar_hsa_circ_260424,RMVar_hsa_circ_113359,RMVar_hsa_circ_115440,RMVar_hsa_circ_260425 49200 RMVar_ID_49200 Human_SNP_ID_416716033 A-to-I Human chr9 + 131400592 131400592 131400592 CACCTGCCTTGGCCTCCCAAAGTGCTGGGATGACAGGTGTGAGCCACCGTGCCTGGACACCCAGG CACCTGCCTTGGCCTCCCAAAGTGCTGGGATGGCAGGTGTGAGCCACCGTGCCTGGACACCCAGG A G PRRC2B Ensembl:ENSG00000130723 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs373165146 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_260424,RMVar_hsa_circ_113359,RMVar_hsa_circ_115440,RMVar_hsa_circ_260425 49201 RMVar_ID_49201 Human_SNP_ID_416716386 A-to-I Human chr9 + 131401760 131401760 131401760 TCGGCTCACTGCAGCCTCTGCTTCCTGGGTTTAAGAGATTCTCCTGCCTCAGCCTCCCGAGTAGC TCGGCTCACTGCAGCCTCTGCTTCCTGGGTTTGAGAGATTCTCCTGCCTCAGCCTCCCGAGTAGC A G PRRC2B Ensembl:ENSG00000130723 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs139353609 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16598991 RMVar_hsa_circ_260424,RMVar_hsa_circ_113359,RMVar_hsa_circ_115440,RMVar_hsa_circ_260425 49202 RMVar_ID_49202 Human_SNP_ID_416717222 A-to-I Human chr9 + 131404422 131404422 131404422 TTTTGTATTTTTAATAAAGACGAGATTTCACTATGTTGGCCAGGCTGGTCTCGAACTCTTGACCT TTTTGTATTTTTAATAAAGACGAGATTTCACTGTGTTGGCCAGGCTGGTCTCGAACTCTTGACCT A G PRRC2B Ensembl:ENSG00000130723 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs773852629 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16599129 RMVar_hsa_circ_260424,RMVar_hsa_circ_113359,RMVar_hsa_circ_115440,RMVar_hsa_circ_260425 49203 RMVar_ID_49203 Human_SNP_ID_416717223 A-to-I Human chr9 + 131404422 131404422 131404422 TTTTGTATTTTTAATAAAGACGAGATTTCACTATGTTGGCCAGGCTGGTCTCGAACTCTTGACCT TTTTGTATTTTTAATAAAGACGAGATTTCACTTTGTTGGCCAGGCTGGTCTCGAACTCTTGACCT A T PRRC2B Ensembl:ENSG00000130723 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs773852629 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16599129 RMVar_hsa_circ_260424,RMVar_hsa_circ_113359,RMVar_hsa_circ_115440,RMVar_hsa_circ_260425 49204 RMVar_ID_49204 Human_SNP_ID_416717244 A-to-I Human chr9 + 131404474 131404474 131404474 GAACTCTTGACCTCAGGCGAGCCACCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG GAACTCTTGACCTCAGGCGAGCCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG A G PRRC2B Ensembl:ENSG00000130723 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs529623547 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_260424,RMVar_hsa_circ_113359,RMVar_hsa_circ_115440,RMVar_hsa_circ_260425 49205 RMVar_ID_49205 Human_SNP_ID_416728995 A-to-I Human chr9 + 131443631 131443631 131443631 TTTGTATTTTTTGGTAGAGACAGGGTTTTGCCATGTTGCCCAGGCCGGTCTTGAACTCCTGAGTT TTTGTATTTTTTGGTAGAGACAGGGTTTTGCCGTGTTGCCCAGGCCGGTCTTGAACTCCTGAGTT A G PRRC2B Ensembl:ENSG00000130723 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1359632508 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16600826 RMVar_hsa_circ_3344,RMVar_hsa_circ_347650,RMVar_hsa_circ_354707,RMVar_hsa_circ_377194,RMVar_hsa_circ_366941,RMVar_hsa_circ_311348,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_90380,RMVar_hsa_circ_34553,RMVar_hsa_circ_260429,RMVar_hsa_circ_260431,RMVar_hsa_circ_260430,RMVar_hsa_circ_313327,RMVar_hsa_circ_260427,RMVar_hsa_circ_260428,RMVar_hsa_circ_335846,RMVar_hsa_circ_281372,RMVar_hsa_circ_344873,RMVar_hsa_circ_260439,RMVar_hsa_circ_260440,RMVar_hsa_circ_368739,RMVar_hsa_circ_319124,RMVar_hsa_circ_320506,RMVar_hsa_circ_260441,RMVar_hsa_circ_260443,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 49206 RMVar_ID_49206 Human_SNP_ID_416730323 A-to-I Human chr9 + 131448328 131448320 131448328 ATTCCTTTGGAAGGCTGAGGTGGGCAGATCACAAGATCAGGAGATCGAGACCATCCTGGCTAACA ATTCCTTTGGAAGGCTGAGGTGGGC________AGATCAGGAGATCGAGACCATCCTGGCTAACA CAGATCACA C PRRC2B Ensembl:ENSG00000130723 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1342472982 Functional Loss DEL dbSNP153 26..33 33 - - - Human_RBP_ID_18140698 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 49207 RMVar_ID_49207 Human_SNP_ID_416730993 A-to-I Human chr9 + 131450417 131450417 131450417 AGCCTCCCGAGTAGCTGGAATTATAGGCGCGCACCACATGCCCAACTAATTTTTGTATTTTTAGT AGCCTCCCGAGTAGCTGGAATTATAGGCGCGCGCCACATGCCCAACTAATTTTTGTATTTTTAGT A G PRRC2B Ensembl:ENSG00000130723 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1444375679 Functional Loss SNV dbSNP153 33..33 33 - - - 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 49208 RMVar_ID_49208 Human_SNP_ID_416732406 A-to-I Human chr9 + 131455586 131455586 131455586 TCACCCAGGCTGGAGTGCGGTGGCATGATGTCAGCTCACTAAAACCTCCATCTCCTGGGCTCAGC TCACCCAGGCTGGAGTGCGGTGGCATGATGTCGGCTCACTAAAACCTCCATCTCCTGGGCTCAGC A G PRRC2B Ensembl:ENSG00000130723 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1216186461 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3344,RMVar_hsa_circ_354707,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_260428,RMVar_hsa_circ_335846,RMVar_hsa_circ_344873,RMVar_hsa_circ_260441,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_22227,RMVar_hsa_circ_84564,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_340777,RMVar_hsa_circ_119192,RMVar_hsa_circ_260463,RMVar_hsa_circ_70003,RMVar_hsa_circ_260464,RMVar_hsa_circ_260462 49209 RMVar_ID_49209 Human_SNP_ID_416732433 A-to-I Human chr9 + 131455688 131455688 131455688 CAGATGCACGCCAGCATACCCAGCTAATTTTTATCTTTCTGCTGGAGATGGGGTTTGCCACGTTA CAGATGCACGCCAGCATACCCAGCTAATTTTTGTCTTTCTGCTGGAGATGGGGTTTGCCACGTTA A G PRRC2B Ensembl:ENSG00000130723 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs552141243 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_3344,RMVar_hsa_circ_354707,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_260428,RMVar_hsa_circ_335846,RMVar_hsa_circ_344873,RMVar_hsa_circ_260441,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_22227,RMVar_hsa_circ_84564,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_340777,RMVar_hsa_circ_119192,RMVar_hsa_circ_260463,RMVar_hsa_circ_70003,RMVar_hsa_circ_260464,RMVar_hsa_circ_260462 49210 RMVar_ID_49210 Human_SNP_ID_416733287 A-to-I Human chr9 + 131458703 131458703 131458703 TTTTGTATTTTTAGTAGAGACTTGGTTTCACCATGTTGGCCTGGCTGATCTGGAACTCCTGACCT TTTTGTATTTTTAGTAGAGACTTGGTTTCACCCTGTTGGCCTGGCTGATCTGGAACTCCTGACCT A C PRRC2B Ensembl:ENSG00000130723 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1480155431 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16601433 RMVar_hsa_circ_3344,RMVar_hsa_circ_354707,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_260428,RMVar_hsa_circ_335846,RMVar_hsa_circ_344873,RMVar_hsa_circ_260441,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_22227,RMVar_hsa_circ_84564,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_340777,RMVar_hsa_circ_119192,RMVar_hsa_circ_260463,RMVar_hsa_circ_70003,RMVar_hsa_circ_260464,RMVar_hsa_circ_260462 49211 RMVar_ID_49211 Human_SNP_ID_416733538 A-to-I Human chr9 + 131459504 131459504 131459504 AAAATGTTTTTTCATAGAGACAGGGTCTCACTATGTTGCCCAGGCTTGTCTCAAACTCCAGCTCA AAAATGTTTTTTCATAGAGACAGGGTCTCACTCTGTTGCCCAGGCTTGTCTCAAACTCCAGCTCA A C PRRC2B Ensembl:ENSG00000130723 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs559786413 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16601480 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_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 49212 RMVar_ID_49212 Human_SNP_ID_416733539 A-to-I Human chr9 + 131459504 131459504 131459504 AAAATGTTTTTTCATAGAGACAGGGTCTCACTATGTTGCCCAGGCTTGTCTCAAACTCCAGCTCA AAAATGTTTTTTCATAGAGACAGGGTCTCACTGTGTTGCCCAGGCTTGTCTCAAACTCCAGCTCA A G PRRC2B Ensembl:ENSG00000130723 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs559786413 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16601480 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_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 49213 RMVar_ID_49213 Human_SNP_ID_416734166 A-to-I Human chr9 + 131461730 131461729 131461731 GCCTGGCTAACTTTTGTATTTTTAGTAGAGACAGGGTTTTGCCATGTTGGCCAGGCTGATCTACC GCCTGGCTAACTTTTGTATTTTTAGTAGAGAC__GGTTTTGCCATGTTGGCCAGGCTGATCTACC CAG C PRRC2B Ensembl:ENSG00000130723 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1007753226 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_16760834 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_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 49214 RMVar_ID_49214 Human_SNP_ID_416745002 A-to-I Human chr9 + 131496084 131496084 131496084 ATATATGGCATTGACCCGCTTGCTTTGATACGAAACAAAAAAGCAGACGACTCCTTCATCCCATC ATATATGGCATTGACCCGCTTGCTTTGATACGGAACAAAAAAGCAGACGACTCCTTCATCCCATC A G PRRC2B Ensembl:ENSG00000130723 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs980853123 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2061723,Human_RBP_ID_16602538,Human_RBP_ID_17321467,Human_RBP_ID_17548775,Human_RBP_ID_18197009,Human_RBP_ID_18905094,Human_RBP_ID_21659011,Human_RBP_ID_22116862,Human_RBP_ID_22336807,Human_RBP_ID_22837964,Human_RBP_ID_27132208 49215 RMVar_ID_49215 Human_SNP_ID_416748740 A-to-I Human chr9 + 131508756 131508756 131508756 ATCAAAAGAGATGTGTATTGGGTGATGACTGTATGAGGCCTTGTGTCTATAGAATGTTTTAACAT ATCAAAAGAGATGTGTATTGGGTGATGACTGTGTGAGGCCTTGTGTCTATAGAATGTTTTAACAT A G POMT1 Ensembl:ENSG00000130714 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1035363531 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1702908,Human_RBP_ID_8698691,Human_RBP_ID_16602937 RMVar_hsa_circ_2203,RMVar_hsa_circ_2997,RMVar_hsa_circ_332975,RMVar_hsa_circ_54379,RMVar_hsa_circ_260492,RMVar_hsa_circ_62253,RMVar_hsa_circ_357296,RMVar_hsa_circ_22848,RMVar_hsa_circ_260493 49216 RMVar_ID_49216 Human_SNP_ID_416753494 A-to-I Human chr9 - 131523288 131523288 131523288 TATCTTTATTGTCGAGAAAAAATTAACTTTGCACAAAAGGAGGTGCTCATCAGAGAGCTTTTCAA TATCTTTATTGTCGAGAAAAAATTAACTTTGCGCAAAAGGAGGTGCTCATCAGAGAGCTTTTCAA T C RF00017-4630,RF00017-4498 RNACentral:URS000096585E,RNACentral:URS000099B61A SRP RNA,SRP RNA intron,intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs535816758 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_135 49217 RMVar_ID_49217 Human_SNP_ID_416774945 A-to-I Human chr9 - 131599241 131599241 131599241 TTGTGCCTGTAGTCCTCGCTACTTGGGAGACTAAGGTGGGAGGATGGCTTGAGCCCAGGAGGTCA TTGTGCCTGTAGTCCTCGCTACTTGGGAGACTGAGGTGGGAGGATGGCTTGAGCCCAGGAGGTCA T C RAPGEF1 Ensembl:ENSG00000107263 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs190845346 Functional Loss SNV dbSNP153 33..33 33 - - - 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 49218 RMVar_ID_49218 Human_SNP_ID_416774946 A-to-I Human chr9 - 131599241 131599241 131599241 TTGTGCCTGTAGTCCTCGCTACTTGGGAGACTAAGGTGGGAGGATGGCTTGAGCCCAGGAGGTCA TTGTGCCTGTAGTCCTCGCTACTTGGGAGACTCAGGTGGGAGGATGGCTTGAGCCCAGGAGGTCA T G RAPGEF1 Ensembl:ENSG00000107263 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs190845346 Functional Loss SNV dbSNP153 33..33 33 - - - 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 49219 RMVar_ID_49219 Human_SNP_ID_416775511 A-to-I Human chr9 - 131601671 131601671 131601671 TAACTCCTGGCTTCAAGCGATCCTCCCACATCAGCCTCCCAAAGTGCTGGGCTTACAGGCATGAG TAACTCCTGGCTTCAAGCGATCCTCCCACATCGGCCTCCCAAAGTGCTGGGCTTACAGGCATGAG T C RAPGEF1 Ensembl:ENSG00000107263 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1212873493 Functional Loss SNV dbSNP153 33..33 33 - - - 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 49220 RMVar_ID_49220 Human_SNP_ID_416775524 A-to-I Human chr9 - 131601723 131601723 131601723 GTTTTAGTTTTTTGTAGAGACGAGGTCTCGCTATGTTGCCTAGGATGGTCACTAACTCCTGGCTT GTTTTAGTTTTTTGTAGAGACGAGGTCTCGCTGTGTTGCCTAGGATGGTCACTAACTCCTGGCTT T C RAPGEF1 Ensembl:ENSG00000107263 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs112056492 Functional Loss SNV dbSNP153 33..33 33 - - - 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 49221 RMVar_ID_49221 Human_SNP_ID_416775545 A-to-I Human chr9 - 131601807 131601807 131601807 GAACTCCCGGGCTCAAGCGATCCTCCCACCTCAGCCTCCCAGATAGCTGGGACTACAGGCATGCA GAACTCCCGGGCTCAAGCGATCCTCCCACCTCCGCCTCCCAGATAGCTGGGACTACAGGCATGCA T G RAPGEF1 Ensembl:ENSG00000107263 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs77927761 Functional Loss SNV dbSNP153 33..33 33 - - - 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 49222 RMVar_ID_49222 Human_SNP_ID_416801591 A-to-I Human chr9 - 131711535 131711535 131711535 TGGCCAACGTGGCAGATCCCCCATCTCGACTAAAAATACACAAATTAGCTGGGTGTGGTGGCGCA TGGCCAACGTGGCAGATCCCCCATCTCGACTAGAAATACACAAATTAGCTGGGTGTGGTGGCGCA T C RAPGEF1 Ensembl:ENSG00000107263 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1013463733 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93242,RMVar_hsa_circ_260510 49223 RMVar_ID_49223 Human_SNP_ID_416802368 A-to-I Human chr9 - 131714819 131714819 131714819 CGTATAGTCCCAGCTAGTCAGGAGGCTGAGACAGGAGGATTGCTTGAGCCCAGCAGTTGGAGGCT CGTATAGTCCCAGCTAGTCAGGAGGCTGAGACGGGAGGATTGCTTGAGCCCAGCAGTTGGAGGCT T C RAPGEF1 Ensembl:ENSG00000107263 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs909308620 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93242,RMVar_hsa_circ_260510 49224 RMVar_ID_49224 Human_SNP_ID_416802372 A-to-I Human chr9 - 131714832 131714832 131714832 ATGGTGGCAAGTGCGTATAGTCCCAGCTAGTCAGGAGGCTGAGACAGGAGGATTGCTTGAGCCCA ATGGTGGCAAGTGCGTATAGTCCCAGCTAGTCCGGAGGCTGAGACAGGAGGATTGCTTGAGCCCA T G RAPGEF1 Ensembl:ENSG00000107263 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1421789804 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93242,RMVar_hsa_circ_260510 49225 RMVar_ID_49225 Human_SNP_ID_416802881 A-to-I Human chr9 - 131716734 131716734 131716734 GGGTCTGCCTCTGTCACCCGGGCTGGAGTGCAATGGCGCGATCTTGGCTCACTGCAACCTCTGCC GGGTCTGCCTCTGTCACCCGGGCTGGAGTGCAGTGGCGCGATCTTGGCTCACTGCAACCTCTGCC T C RAPGEF1 Ensembl:ENSG00000107263 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048081159 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93242,RMVar_hsa_circ_260510 49226 RMVar_ID_49226 Human_SNP_ID_416805308 A-to-I Human chr9 - 131726382 131726382 131726382 CCTCAAGTGATCTGCCCGCCTCAGCCTCCCAAAGTGGTGAGATTACAGGTGTGAGCCACTGTGCC CCTCAAGTGATCTGCCCGCCTCAGCCTCCCAAGGTGGTGAGATTACAGGTGTGAGCCACTGTGCC T C RAPGEF1 Ensembl:ENSG00000107263 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1034171936 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93242,RMVar_hsa_circ_260510 49227 RMVar_ID_49227 Human_SNP_ID_416887761 A-to-I Human chr9 + 132068821 132068821 132068821 ATACATGGGTCTGGATGTCGAGGGAGGGAGCCAGCCTGGTGATGGAGTTAGATGTCATTGTGTGT ATACATGGGTCTGGATGTCGAGGGAGGGAGCCGGCCTGGTGATGGAGTTAGATGTCATTGTGTGT A G NONHSAG053659.2 RNACentral:URS00009C0B2B lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1052610405 Functional Loss SNV dbSNP153 33..33 33 - - - 49228 RMVar_ID_49228 Human_SNP_ID_416940530 A-to-I Human chr9 - 132268401 132268401 132268401 CGCCTCCTGGATTTAAGCCGTTCTCCCACCTCAGCCTCCTGAGTAGCTGAGACTATAGGCGCATG CGCCTCCTGGATTTAAGCCGTTCTCCCACCTCGGCCTCCTGAGTAGCTGAGACTATAGGCGCATG T C SETX Ensembl:ENSG00000107290 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs754187041 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119175,RMVar_hsa_circ_260528,RMVar_hsa_circ_111763,RMVar_hsa_circ_111994,RMVar_hsa_circ_260529,RMVar_hsa_circ_260527 49229 RMVar_ID_49229 Human_SNP_ID_416940532 A-to-I Human chr9 - 132268406 132268406 132268406 GCCTCCGCCTCCTGGATTTAAGCCGTTCTCCCACCTCAGCCTCCTGAGTAGCTGAGACTATAGGC GCCTCCGCCTCCTGGATTTAAGCCGTTCTCCCGCCTCAGCCTCCTGAGTAGCTGAGACTATAGGC T C SETX Ensembl:ENSG00000107290 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1245544037 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119175,RMVar_hsa_circ_260528,RMVar_hsa_circ_111763,RMVar_hsa_circ_111994,RMVar_hsa_circ_260529,RMVar_hsa_circ_260527 49230 RMVar_ID_49230 Human_SNP_ID_416940548 A-to-I Human chr9 - 132268457 132268457 132268457 AAGTTGTTTTCCCCTGGCGGGAGTGCAGTGGCACAATCACAGCTCACTGCAGCCTCCGCCTCCTG AAGTTGTTTTCCCCTGGCGGGAGTGCAGTGGCGCAATCACAGCTCACTGCAGCCTCCGCCTCCTG T C SETX Ensembl:ENSG00000107290 Protein coding intron GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,31158229,31158229 RNA-Seq:(High) rs1240645412 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119175,RMVar_hsa_circ_260528,RMVar_hsa_circ_111763,RMVar_hsa_circ_111994,RMVar_hsa_circ_260529,RMVar_hsa_circ_260527 49231 RMVar_ID_49231 Human_SNP_ID_416941659 A-to-I Human chr9 - 132272424 132272424 132272424 GACTGTAAGGCCAGGCATGGTGGCTCACATCTATAATCCTAACATTTTGGGTGGGTGAGGTGGAA GACTGTAAGGCCAGGCATGGTGGCTCACATCTGTAATCCTAACATTTTGGGTGGGTGAGGTGGAA T C SETX Ensembl:ENSG00000107290 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs911699715 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23090783 RMVar_hsa_circ_229,RMVar_hsa_circ_119175,RMVar_hsa_circ_64633,RMVar_hsa_circ_260528,RMVar_hsa_circ_111763,RMVar_hsa_circ_111994,RMVar_hsa_circ_260529,RMVar_hsa_circ_124246,RMVar_hsa_circ_260527,RMVar_hsa_circ_77539,RMVar_hsa_circ_28630,RMVar_hsa_circ_260531,RMVar_hsa_circ_260532,RMVar_hsa_circ_365932,RMVar_hsa_circ_12543,RMVar_hsa_circ_265569,RMVar_hsa_circ_268912,RMVar_hsa_circ_310637,RMVar_hsa_circ_376988,RMVar_hsa_circ_335348,RMVar_hsa_circ_284317,RMVar_hsa_circ_268816,RMVar_hsa_circ_260534,RMVar_hsa_circ_260535 49232 RMVar_ID_49232 Human_SNP_ID_416941666 A-to-I Human chr9 - 132272444 132272444 132272444 TAAGTTTCTTTAAAAATAAAGACTGTAAGGCCAGGCATGGTGGCTCACATCTATAATCCTAACAT TAAGTTTCTTTAAAAATAAAGACTGTAAGGCCGGGCATGGTGGCTCACATCTATAATCCTAACAT T C SETX Ensembl:ENSG00000107290 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs943201855 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16606212 RMVar_hsa_circ_229,RMVar_hsa_circ_119175,RMVar_hsa_circ_64633,RMVar_hsa_circ_260528,RMVar_hsa_circ_111763,RMVar_hsa_circ_111994,RMVar_hsa_circ_260529,RMVar_hsa_circ_124246,RMVar_hsa_circ_260527,RMVar_hsa_circ_77539,RMVar_hsa_circ_28630,RMVar_hsa_circ_260531,RMVar_hsa_circ_260532,RMVar_hsa_circ_365932,RMVar_hsa_circ_12543,RMVar_hsa_circ_265569,RMVar_hsa_circ_268912,RMVar_hsa_circ_310637,RMVar_hsa_circ_376988,RMVar_hsa_circ_335348,RMVar_hsa_circ_284317,RMVar_hsa_circ_268816,RMVar_hsa_circ_260534,RMVar_hsa_circ_260535 49233 RMVar_ID_49233 Human_SNP_ID_416944300 A-to-I Human chr9 - 132281936 132281936 132281936 CTCACTGCAACCTCTGCCTCCTGGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCCAAGTAGCTGGG CTCACTGCAACCTCTGCCTCCTGGGTTCAAGCCGTTCTCCTGCCTCAGCCTCCCAAGTAGCTGGG T G SETX Ensembl:ENSG00000107290 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1223427832 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_229,RMVar_hsa_circ_119175,RMVar_hsa_circ_64633,RMVar_hsa_circ_260528,RMVar_hsa_circ_111763,RMVar_hsa_circ_111994,RMVar_hsa_circ_260529,RMVar_hsa_circ_260527,RMVar_hsa_circ_77539,RMVar_hsa_circ_260532,RMVar_hsa_circ_365932,RMVar_hsa_circ_12543,RMVar_hsa_circ_55744,RMVar_hsa_circ_300883,RMVar_hsa_circ_265569,RMVar_hsa_circ_268912,RMVar_hsa_circ_335348,RMVar_hsa_circ_338540,RMVar_hsa_circ_342766,RMVar_hsa_circ_355914,RMVar_hsa_circ_341992,RMVar_hsa_circ_51953,RMVar_hsa_circ_268548,RMVar_hsa_circ_300283,RMVar_hsa_circ_61479,RMVar_hsa_circ_260536,RMVar_hsa_circ_260537,RMVar_hsa_circ_105846,RMVar_hsa_circ_358924,RMVar_hsa_circ_260539,RMVar_hsa_circ_55756,RMVar_hsa_circ_114919,RMVar_hsa_circ_299002,RMVar_hsa_circ_316536,RMVar_hsa_circ_120715,RMVar_hsa_circ_75289,RMVar_hsa_circ_260542,RMVar_hsa_circ_260543,RMVar_hsa_circ_260544 49234 RMVar_ID_49234 Human_SNP_ID_416946784 A-to-I Human chr9 - 132290040 132290040 132290040 CATGCCTGGCTAATTTTTTTATTTTTAGTAGAAATGGGGTTTTGCCATGTTGGCCAGGCTCGTCT CATGCCTGGCTAATTTTTTTATTTTTAGTAGAGATGGGGTTTTGCCATGTTGGCCAGGCTCGTCT T C SETX Ensembl:ENSG00000107290 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1165581374 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16606395 RMVar_hsa_circ_119175,RMVar_hsa_circ_64633,RMVar_hsa_circ_260528,RMVar_hsa_circ_111763,RMVar_hsa_circ_111994,RMVar_hsa_circ_260529,RMVar_hsa_circ_260527,RMVar_hsa_circ_365932,RMVar_hsa_circ_55475,RMVar_hsa_circ_55744,RMVar_hsa_circ_300883,RMVar_hsa_circ_268912,RMVar_hsa_circ_335348,RMVar_hsa_circ_338540,RMVar_hsa_circ_342766,RMVar_hsa_circ_51953,RMVar_hsa_circ_268548,RMVar_hsa_circ_61479,RMVar_hsa_circ_260536,RMVar_hsa_circ_260537,RMVar_hsa_circ_105846,RMVar_hsa_circ_358924,RMVar_hsa_circ_260539,RMVar_hsa_circ_55756,RMVar_hsa_circ_114919,RMVar_hsa_circ_299002,RMVar_hsa_circ_120715,RMVar_hsa_circ_260542,RMVar_hsa_circ_260543,RMVar_hsa_circ_260544,RMVar_hsa_circ_292636,RMVar_hsa_circ_360568,RMVar_hsa_circ_260546,RMVar_hsa_circ_1449,RMVar_hsa_circ_339266,RMVar_hsa_circ_260545,RMVar_hsa_circ_357847,RMVar_hsa_circ_74207,RMVar_hsa_circ_260547,RMVar_hsa_circ_337182,RMVar_hsa_circ_349319,RMVar_hsa_circ_260549,RMVar_hsa_circ_265135,RMVar_hsa_circ_269114 49235 RMVar_ID_49235 Human_SNP_ID_416947144 A-to-I Human chr9 - 132291209 132291209 132291209 AGAGCCGAGATTGCGCCATTGCACTCCAGCCTAGGAGACAGAGCAAGACTCCGTCTCAAAAAAAA AGAGCCGAGATTGCGCCATTGCACTCCAGCCTGGGAGACAGAGCAAGACTCCGTCTCAAAAAAAA T C SETX Ensembl:ENSG00000107290 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1234005035 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119175,RMVar_hsa_circ_64633,RMVar_hsa_circ_260528,RMVar_hsa_circ_111763,RMVar_hsa_circ_111994,RMVar_hsa_circ_260529,RMVar_hsa_circ_260527,RMVar_hsa_circ_365932,RMVar_hsa_circ_55475,RMVar_hsa_circ_55744,RMVar_hsa_circ_300883,RMVar_hsa_circ_268912,RMVar_hsa_circ_335348,RMVar_hsa_circ_338540,RMVar_hsa_circ_342766,RMVar_hsa_circ_51953,RMVar_hsa_circ_268548,RMVar_hsa_circ_61479,RMVar_hsa_circ_260536,RMVar_hsa_circ_260537,RMVar_hsa_circ_105846,RMVar_hsa_circ_358924,RMVar_hsa_circ_260539,RMVar_hsa_circ_55756,RMVar_hsa_circ_114919,RMVar_hsa_circ_299002,RMVar_hsa_circ_120715,RMVar_hsa_circ_260542,RMVar_hsa_circ_260543,RMVar_hsa_circ_260544,RMVar_hsa_circ_292636,RMVar_hsa_circ_360568,RMVar_hsa_circ_260546,RMVar_hsa_circ_1449,RMVar_hsa_circ_339266,RMVar_hsa_circ_260545,RMVar_hsa_circ_357847,RMVar_hsa_circ_74207,RMVar_hsa_circ_260547,RMVar_hsa_circ_337182,RMVar_hsa_circ_349319,RMVar_hsa_circ_260549,RMVar_hsa_circ_265135,RMVar_hsa_circ_269114 49236 RMVar_ID_49236 Human_SNP_ID_416947443 A-to-I Human chr9 - 132292257 132292257 132292257 TGGGTTAATTTTTAAATTTTTGTTGTAGAGACAGGGTCTCCTCGTGTTGCCCAGGCTGGCTTCAA TGGGTTAATTTTTAAATTTTTGTTGTAGAGACCGGGTCTCCTCGTGTTGCCCAGGCTGGCTTCAA T G SETX Ensembl:ENSG00000107290 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs575786612 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119175,RMVar_hsa_circ_64633,RMVar_hsa_circ_260528,RMVar_hsa_circ_111763,RMVar_hsa_circ_111994,RMVar_hsa_circ_260529,RMVar_hsa_circ_260527,RMVar_hsa_circ_365932,RMVar_hsa_circ_55475,RMVar_hsa_circ_55744,RMVar_hsa_circ_300883,RMVar_hsa_circ_268912,RMVar_hsa_circ_335348,RMVar_hsa_circ_338540,RMVar_hsa_circ_342766,RMVar_hsa_circ_51953,RMVar_hsa_circ_268548,RMVar_hsa_circ_61479,RMVar_hsa_circ_260536,RMVar_hsa_circ_260537,RMVar_hsa_circ_105846,RMVar_hsa_circ_358924,RMVar_hsa_circ_260539,RMVar_hsa_circ_55756,RMVar_hsa_circ_114919,RMVar_hsa_circ_299002,RMVar_hsa_circ_120715,RMVar_hsa_circ_260542,RMVar_hsa_circ_260543,RMVar_hsa_circ_260544,RMVar_hsa_circ_292636,RMVar_hsa_circ_360568,RMVar_hsa_circ_260546,RMVar_hsa_circ_1449,RMVar_hsa_circ_339266,RMVar_hsa_circ_260545,RMVar_hsa_circ_357847,RMVar_hsa_circ_74207,RMVar_hsa_circ_260547,RMVar_hsa_circ_337182,RMVar_hsa_circ_349319,RMVar_hsa_circ_260549,RMVar_hsa_circ_265135,RMVar_hsa_circ_269114 49237 RMVar_ID_49237 Human_SNP_ID_416947977 A-to-I Human chr9 - 132294033 132294025 132294033 GGTGTCTAGGTTGGATATTTATTTATTTATTTATTTATTTTTGAGACGGAGTCTCACCCTGTCGC GGTGTCTAGGTTGGATATTTATTTATTTATTT________TTGAGACGGAGTCTCACCCTGTCGC AAAATAAAT A SETX Ensembl:ENSG00000107290 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs553767403 Functional Loss DEL dbSNP153 33..40 33 - - - RMVar_hsa_circ_119175,RMVar_hsa_circ_64633,RMVar_hsa_circ_260528,RMVar_hsa_circ_111763,RMVar_hsa_circ_111994,RMVar_hsa_circ_260529,RMVar_hsa_circ_260527,RMVar_hsa_circ_365932,RMVar_hsa_circ_55475,RMVar_hsa_circ_55744,RMVar_hsa_circ_300883,RMVar_hsa_circ_268912,RMVar_hsa_circ_335348,RMVar_hsa_circ_338540,RMVar_hsa_circ_342766,RMVar_hsa_circ_51953,RMVar_hsa_circ_268548,RMVar_hsa_circ_61479,RMVar_hsa_circ_260536,RMVar_hsa_circ_260537,RMVar_hsa_circ_105846,RMVar_hsa_circ_358924,RMVar_hsa_circ_260539,RMVar_hsa_circ_55756,RMVar_hsa_circ_114919,RMVar_hsa_circ_299002,RMVar_hsa_circ_120715,RMVar_hsa_circ_260542,RMVar_hsa_circ_260543,RMVar_hsa_circ_260544,RMVar_hsa_circ_292636,RMVar_hsa_circ_360568,RMVar_hsa_circ_260546,RMVar_hsa_circ_1449,RMVar_hsa_circ_339266,RMVar_hsa_circ_260545,RMVar_hsa_circ_357847,RMVar_hsa_circ_74207,RMVar_hsa_circ_260547,RMVar_hsa_circ_337182,RMVar_hsa_circ_349319,RMVar_hsa_circ_260549,RMVar_hsa_circ_265135,RMVar_hsa_circ_269114 49238 RMVar_ID_49238 Human_SNP_ID_416947978 A-to-I Human chr9 - 132294033 132294025 132294033 GGTGTCTAGGTTGGATATTTATTTATTTATTTATTTATTTTTGAGACGGAGTCTCACCCTGTCGC GGTGTCTAGGTTGGATATTTATTTATTTATTT____ATTTTTGAGACGGAGTCTCACCCTGTCGC AAAATAAAT AAAAT SETX Ensembl:ENSG00000107290 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs553767403 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_119175,RMVar_hsa_circ_64633,RMVar_hsa_circ_260528,RMVar_hsa_circ_111763,RMVar_hsa_circ_111994,RMVar_hsa_circ_260529,RMVar_hsa_circ_260527,RMVar_hsa_circ_365932,RMVar_hsa_circ_55475,RMVar_hsa_circ_55744,RMVar_hsa_circ_300883,RMVar_hsa_circ_268912,RMVar_hsa_circ_335348,RMVar_hsa_circ_338540,RMVar_hsa_circ_342766,RMVar_hsa_circ_51953,RMVar_hsa_circ_268548,RMVar_hsa_circ_61479,RMVar_hsa_circ_260536,RMVar_hsa_circ_260537,RMVar_hsa_circ_105846,RMVar_hsa_circ_358924,RMVar_hsa_circ_260539,RMVar_hsa_circ_55756,RMVar_hsa_circ_114919,RMVar_hsa_circ_299002,RMVar_hsa_circ_120715,RMVar_hsa_circ_260542,RMVar_hsa_circ_260543,RMVar_hsa_circ_260544,RMVar_hsa_circ_292636,RMVar_hsa_circ_360568,RMVar_hsa_circ_260546,RMVar_hsa_circ_1449,RMVar_hsa_circ_339266,RMVar_hsa_circ_260545,RMVar_hsa_circ_357847,RMVar_hsa_circ_74207,RMVar_hsa_circ_260547,RMVar_hsa_circ_337182,RMVar_hsa_circ_349319,RMVar_hsa_circ_260549,RMVar_hsa_circ_265135,RMVar_hsa_circ_269114 49239 RMVar_ID_49239 Human_SNP_ID_416953637 A-to-I Human chr9 - 132314496 132314496 132314496 AAGCTAGCCGGGCTTGGTGGCTCACATCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGTAGA AAGCTAGCCGGGCTTGGTGGCTCACATCTGTAGTCCCAGCACTTTGGGAGGCCGAGGTGGGTAGA T C SETX Ensembl:ENSG00000107290 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs758196297 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119175,RMVar_hsa_circ_260528,RMVar_hsa_circ_111763,RMVar_hsa_circ_260529,RMVar_hsa_circ_55475,RMVar_hsa_circ_268912,RMVar_hsa_circ_338540,RMVar_hsa_circ_342766,RMVar_hsa_circ_268548,RMVar_hsa_circ_260537,RMVar_hsa_circ_105846,RMVar_hsa_circ_260539,RMVar_hsa_circ_55756,RMVar_hsa_circ_268915,RMVar_hsa_circ_260545,RMVar_hsa_circ_269114,RMVar_hsa_circ_65132,RMVar_hsa_circ_260551,RMVar_hsa_circ_317034,RMVar_hsa_circ_260555,RMVar_hsa_circ_320538,RMVar_hsa_circ_288156 49240 RMVar_ID_49240 Human_SNP_ID_416955155 A-to-I Human chr9 - 132320341 132320341 132320341 TCAATCTTCTGACCTTGTGATCTGCTCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG TCAATCTTCTGACCTTGTGATCTGCTCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG T C SETX Ensembl:ENSG00000107290 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs542509803 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16606794 RMVar_hsa_circ_119175,RMVar_hsa_circ_260528,RMVar_hsa_circ_111763,RMVar_hsa_circ_260529,RMVar_hsa_circ_55475,RMVar_hsa_circ_268912,RMVar_hsa_circ_338540,RMVar_hsa_circ_342766,RMVar_hsa_circ_268548,RMVar_hsa_circ_260537,RMVar_hsa_circ_105846,RMVar_hsa_circ_260539,RMVar_hsa_circ_55756,RMVar_hsa_circ_268915,RMVar_hsa_circ_260545,RMVar_hsa_circ_269114,RMVar_hsa_circ_65132,RMVar_hsa_circ_260551,RMVar_hsa_circ_317034,RMVar_hsa_circ_260555,RMVar_hsa_circ_320538,RMVar_hsa_circ_288156 49241 RMVar_ID_49241 Human_SNP_ID_416964027 A-to-I Human chr9 - 132347596 132347596 132347596 CTACAAGAGAAGTGTTTAAGGCTGAGTGCTGTAGCTTACACCTGTAATCCCAGCACTTTGGGATG CTACAAGAGAAGTGTTTAAGGCTGAGTGCTGTGGCTTACACCTGTAATCCCAGCACTTTGGGATG T C SETX Ensembl:ENSG00000107290 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1296873641 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119175,RMVar_hsa_circ_260529,RMVar_hsa_circ_338540,RMVar_hsa_circ_342766,RMVar_hsa_circ_260537,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,RMVar_hsa_circ_260560,RMVar_hsa_circ_260558,RMVar_hsa_circ_305975,RMVar_hsa_circ_325136,RMVar_hsa_circ_273822,RMVar_hsa_circ_29599 49242 RMVar_ID_49242 Human_SNP_ID_417073073 A-to-I Human chr9 + 132765218 132765218 132765218 GGGAGGCTGAGGCGGGAGAGTTGCTTGAGCCCAGGGGGCGGAGGTTGTAGTGAGCCAAGATCATG GGGAGGCTGAGGCGGGAGAGTTGCTTGAGCCCGGGGGGCGGAGGTTGTAGTGAGCCAAGATCATG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs534756379 Functional Loss SNV dbSNP153 33..33 33 - - - 49243 RMVar_ID_49243 Human_SNP_ID_417103801 A-to-I Human chr9 + 132888989 132888989 132888989 CAGCGTTTCACCATGTTAGCCAGGATGGTCTCAATCTCCTGACCTCATGATCTACCCTCGTGATC CAGCGTTTCACCATGTTAGCCAGGATGGTCTCGATCTCCTGACCTCATGATCTACCCTCGTGATC A G SPACA9 Ensembl:ENSG00000165698 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs546380161 Functional Loss SNV dbSNP153 33..33 33 - - - Clinvar_Rec_136 RMVar_hsa_circ_87370,RMVar_hsa_circ_260586 49244 RMVar_ID_49244 Human_SNP_ID_417147186 A-to-I Human chr9 + 133053049 133053049 133053049 TTTAGTAGAGATGGGGTTTCGCCATGTTGGTCAGGCTGGTCTCGAACTCCTAACCTCAAGTGATC TTTAGTAGAGATGGGGTTTCGCCATGTTGGTCGGGCTGGTCTCGAACTCCTAACCTCAAGTGATC A G GTF3C5 Ensembl:ENSG00000148308 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1033746273 Functional Loss SNV dbSNP153 33..33 33 - - - 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 49245 RMVar_ID_49245 Human_SNP_ID_417148984 A-to-I Human chr9 + 133058427 133058427 133058427 TCTCACGTGGCAAGAAGTGCCTTTAGCTCTGGATCCCAACCGTTTGGCACAGCTTTGGCCACAGC TCTCACGTGGCAAGAAGTGCCTTTAGCTCTGGGTCCCAACCGTTTGGCACAGCTTTGGCCACAGC A G GTF3C5 Ensembl:ENSG00000148308 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs189175834 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_714155,Human_RBP_ID_1058450,Human_RBP_ID_1226556,Human_RBP_ID_1703097,Human_RBP_ID_2061973,Human_RBP_ID_8699147,Human_RBP_ID_16610314,Human_RBP_ID_17321572,Human_RBP_ID_18905506,Human_RBP_ID_22838034,Human_RBP_ID_24291101,Human_RBP_ID_26565511 Human_miRNA_ID_1606604,Human_miRNA_ID_1680857,Human_miRNA_ID_2824894,Human_miRNA_ID_2858864 RMVar_hsa_circ_90557,RMVar_hsa_circ_260603,RMVar_hsa_circ_108176,RMVar_hsa_circ_260604,RMVar_hsa_circ_82287,RMVar_hsa_circ_260608,RMVar_hsa_circ_111406,RMVar_hsa_circ_85546,RMVar_hsa_circ_121405,RMVar_hsa_circ_260610,RMVar_hsa_circ_260611,RMVar_hsa_circ_122022,RMVar_hsa_circ_260613,RMVar_hsa_circ_119240,RMVar_hsa_circ_260614,RMVar_hsa_circ_260615 49246 RMVar_ID_49246 Human_SNP_ID_417149551 A-to-I Human chr9 + 133060311 133060311 133060311 AAAATCGGCTGGGTGTGATGGCGCACGCCTGTAATCCCAGCTACTTCAGAGGCTAAAGCAGGAGG AAAATCGGCTGGGTGTGATGGCGCACGCCTGTGATCCCAGCTACTTCAGAGGCTAAAGCAGGAGG A G RF00017-4643 RNACentral:URS00009A02E8 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1185988041 Functional Loss SNV dbSNP153 33..33 33 - - - 49247 RMVar_ID_49247 Human_SNP_ID_417178764 A-to-I Human chr9 - 133160032 133160032 133160032 CCCCTCATCGGCCTCCCAAAGTGCTGGGATTAAAGGCGTGAACCACCACCCCTGGCCTTAATTTT CCCCTCATCGGCCTCCCAAAGTGCTGGGATTAGAGGCGTGAACCACCACCCCTGGCCTTAATTTT T C AL162417.1,GBGT1 Ensembl:ENSG00000285245,Ensembl:ENSG00000148288 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs989797755 Functional Loss SNV dbSNP153 33..33 33 - - - 49248 RMVar_ID_49248 Human_SNP_ID_417178789 A-to-I Human chr9 - 133160118 133160118 133160118 CACACGCTAATTTTTGTATTTTTAGTAGAAACAGCATTTCATCATGTTGGCCAGGTTGGTCTTTG CACACGCTAATTTTTGTATTTTTAGTAGAAACGGCATTTCATCATGTTGGCCAGGTTGGTCTTTG T C AL162417.1,GBGT1 Ensembl:ENSG00000285245,Ensembl:ENSG00000148288 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1038614147 Functional Loss SNV dbSNP153 33..33 33 - - - 49249 RMVar_ID_49249 Human_SNP_ID_417224684 A-to-I Human chr9 - 133337676 133337676 133337676 ATATATCTTGAGACAGCCTGGCACTCCAGGCTAGAATGCAGTGGCGTGATCTTGGCTCACTGTAA ATATATCTTGAGACAGCCTGGCACTCCAGGCTGGAATGCAGTGGCGTGATCTTGGCTCACTGTAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1486597514 Functional Loss SNV dbSNP153 33..33 33 - - - 49250 RMVar_ID_49250 Human_SNP_ID_417250805 A-to-I Human chr9 + 133419021 133419021 133419021 CGCCACCACTCTCTGCCAATTTTTGTATTTTTAGTAGACCTGGGGTTTCGCCACGTTGGCCAGGC CGCCACCACTCTCTGCCAATTTTTGTATTTTTGGTAGACCTGGGGTTTCGCCACGTTGGCCAGGC A G ADAMTS13 Ensembl:ENSG00000160323 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1386423041 Functional Loss SNV dbSNP153 33..33 33 - - - 49251 RMVar_ID_49251 Human_SNP_ID_417251342 A-to-I Human chr9 + 133421010 133421010 133421010 CAGAGTGTCTGGGCTTGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGTCAG CAGAGTGTCTGGGCTTGGTGGCTCATGCCTGTGATCCCAGCACTTTGGGAGGCCGAGGCAGTCAG A G ADAMTS13 Ensembl:ENSG00000160323 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs3118666 Functional Loss SNV dbSNP153,PGA 33..33 33 - - - 49252 RMVar_ID_49252 Human_SNP_ID_417251379 A-to-I Human chr9 + 133421145 133421145 133421145 AAAACTAGCCAGGCGTGATGGCGGGTGCCTGTAATCCCAGCCACAAGGGAGGCTGAGGCAGGAGA AAAACTAGCCAGGCGTGATGGCGGGTGCCTGTTATCCCAGCCACAAGGGAGGCTGAGGCAGGAGA A T ADAMTS13 Ensembl:ENSG00000160323 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs945764042 Functional Loss SNV dbSNP153 33..33 33 - - - 49253 RMVar_ID_49253 Human_SNP_ID_417348367 A-to-I Human chr9 - 133757143 133757143 133757143 AATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATCTTGGCCAGGCTGGTCTTGAACTCCTAA AATTTTTGTATTTTTAGTAGAGACGGGGTTTCGCCATCTTGGCCAGGCTGGTCTTGAACTCCTAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946371870 Functional Loss SNV dbSNP153 33..33 33 - - - 49254 RMVar_ID_49254 Human_SNP_ID_417370476 A-to-I Human chr9 - 133831263 133831263 133831263 CCCGGCTAATTTTTGTATTTTTAGTAGAGACAAGGTTTCACCGTGTTGGCCAGGCTGGTCTTGGG CCCGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCGTGTTGGCCAGGCTGGTCTTGGG T C VAV2 Ensembl:ENSG00000160293 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs545418748 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 49255 RMVar_ID_49255 Human_SNP_ID_417390265 A-to-I Human chr9 - 133899494 133899494 133899494 TAAGGCATGAGAATCGCTTGAACCCAGGAGGCAGAGATTGCGGTGAGCTCAGATCGTGCTATAGG TAAGGCATGAGAATCGCTTGAACCCAGGAGGCGGAGATTGCGGTGAGCTCAGATCGTGCTATAGG T C VAV2 Ensembl:ENSG00000160293 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404071496 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_376386,RMVar_hsa_circ_260689,RMVar_hsa_circ_260692,RMVar_hsa_circ_295080,RMVar_hsa_circ_311197,RMVar_hsa_circ_260693 49256 RMVar_ID_49256 Human_SNP_ID_417430554 A-to-I Human chr9 + 134036931 134036931 134036931 TATGCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCAGGGAGGCGGAGGCTGCAGTGAGCCAAGA TATGCGGGAGGCTGAGGCAGGAGAATCGCTTGTACCAGGGAGGCGGAGGCTGCAGTGAGCCAAGA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037737718 Functional Loss SNV dbSNP153 33..33 33 - - - 49257 RMVar_ID_49257 Human_SNP_ID_417433962 A-to-I Human chr9 - 134048200 134048200 134048200 CGCTACTGCGACAGCATCCTCAGGGAGATGCTATCCAAGAAGCACGCGGCCTACGCCTGGCCCTT CGCTACTGCGACAGCATCCTCAGGGAGATGCTGTCCAAGAAGCACGCGGCCTACGCCTGGCCCTT T C BRD3 Ensembl:ENSG00000169925 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs376166015 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8926913,Human_RBP_ID_27833595 RMVar_hsa_circ_81050,RMVar_hsa_circ_260697,RMVar_hsa_circ_52676,RMVar_hsa_circ_260698,RMVar_hsa_circ_373881 49258 RMVar_ID_49258 Human_SNP_ID_417462497 A-to-I Human chr9 + 134143631 134143631 134143631 TCACTGCAAGCTCCGCCTCCCGGGTTCATGCCATTCTCCTGCCTCAGCCTCTCCGAGTAGTTGAG TCACTGCAAGCTCCGCCTCCCGGGTTCATGCCGTTCTCCTGCCTCAGCCTCTCCGAGTAGTTGAG A G WDR5 Ensembl:ENSG00000196363 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1469657392 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7484,RMVar_hsa_circ_47471,RMVar_hsa_circ_310348,RMVar_hsa_circ_274086,RMVar_hsa_circ_9170,RMVar_hsa_circ_104421,RMVar_hsa_circ_303693,RMVar_hsa_circ_260704,RMVar_hsa_circ_260707,RMVar_hsa_circ_80073,RMVar_hsa_circ_260706 49259 RMVar_ID_49259 Human_SNP_ID_417462509 A-to-I Human chr9 + 134143667 134143667 134143667 TCCTGCCTCAGCCTCTCCGAGTAGTTGAGACTACAGGCGCCCACCACCATGCCTGGCTAATTTTT TCCTGCCTCAGCCTCTCCGAGTAGTTGAGACTGCAGGCGCCCACCACCATGCCTGGCTAATTTTT A G WDR5 Ensembl:ENSG00000196363 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs565707842 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7484,RMVar_hsa_circ_47471,RMVar_hsa_circ_310348,RMVar_hsa_circ_274086,RMVar_hsa_circ_9170,RMVar_hsa_circ_104421,RMVar_hsa_circ_303693,RMVar_hsa_circ_260704,RMVar_hsa_circ_260707,RMVar_hsa_circ_80073,RMVar_hsa_circ_260706 49260 RMVar_ID_49260 Human_SNP_ID_417462800 A-to-I Human chr9 + 134144569 134144569 134144569 TCATAAAAAAACACAAAAACAGGTTGGGTGCCATGTCTCCCACCTGTAATTCCAGCACTTTGGGT TCATAAAAAAACACAAAAACAGGTTGGGTGCCGTGTCTCCCACCTGTAATTCCAGCACTTTGGGT A G WDR5 Ensembl:ENSG00000196363 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4130591 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16612770 RMVar_hsa_circ_7484,RMVar_hsa_circ_47471,RMVar_hsa_circ_310348,RMVar_hsa_circ_274086,RMVar_hsa_circ_9170,RMVar_hsa_circ_104421,RMVar_hsa_circ_303693,RMVar_hsa_circ_260704,RMVar_hsa_circ_260707,RMVar_hsa_circ_80073,RMVar_hsa_circ_260706 49261 RMVar_ID_49261 Human_SNP_ID_417469750 A-to-I Human chr9 + 134167313 134167313 134167313 TTGGCTCACTGCAACCTCCGTCTTCCGGATTCAAGCGATTCTCTGGCCTTAGCCTCCTGAGTAGA TTGGCTCACTGCAACCTCCGTCTTCCGGATTCCAGCGATTCTCTGGCCTTAGCCTCCTGAGTAGA A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1554729758 Functional Loss SNV dbSNP153 33..33 33 - - - 49262 RMVar_ID_49262 Human_SNP_ID_417469761 A-to-I Human chr9 + 134167343 134167343 134167343 TCAAGCGATTCTCTGGCCTTAGCCTCCTGAGTAGATGGGATTACAGGCGCACACCACCACACCCG TCAAGCGATTCTCTGGCCTTAGCCTCCTGAGTCGATGGGATTACAGGCGCACACCACCACACCCG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025255809 Functional Loss SNV dbSNP153 33..33 33 - - - 49263 RMVar_ID_49263 Human_SNP_ID_676009768 A-to-I Human chr20 + 20018328 20018328 20018328 CTTTTCCTGGATTCTGCAGTTAACATTTTGCTACGCTGGTATCTCTCCTTCCTTCCCATCTATCA CTTTTCCTGGATTCTGCAGTTAACATTTTGCTGCGCTGGTATCTCTCCTTCCTTCCCATCTATCA A G NAA20 Ensembl:ENSG00000173418 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1396571666 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_208962,RMVar_hsa_circ_127399 49264 RMVar_ID_49264 Human_SNP_ID_676009783 A-to-I Human chr20 + 20018377 20018377 20018377 TCCTTCCCATCTATCAGTCCTGGATCCACTTTAAAAAAACAACAGGGCGGTATGTGAAAACTAAG TCCTTCCCATCTATCAGTCCTGGATCCACTTTTAAAAAACAACAGGGCGGTATGTGAAAACTAAG A T NAA20 Ensembl:ENSG00000173418 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1272773423 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2064978 RMVar_hsa_circ_208962,RMVar_hsa_circ_127399 49265 RMVar_ID_49265 Human_SNP_ID_676009793 A-to-I Human chr20 + 20018407 20018407 20018407 TTAAAAAAACAACAGGGCGGTATGTGAAAACTAAGGACAAAGTGGTTCCGATTCAAGTGTCAGGA TTAAAAAAACAACAGGGCGGTATGTGAAAACTGAGGACAAAGTGGTTCCGATTCAAGTGTCAGGA A G NAA20 Ensembl:ENSG00000173418 Protein coding exon GSE100210;GSE107867 HepG2 cell line;ASD brains,cerebellum - 29129909,30559470 RNA-Seq:(High) rs1416565917 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2064978 RMVar_hsa_circ_208962,RMVar_hsa_circ_127399 49266 RMVar_ID_49266 Human_SNP_ID_676009805 A-to-I Human chr20 + 20018454 20018454 20018454 CCGATTCAAGTGTCAGGAAGATGGAAAGAACTATGGGATAAGATGGCTGGGAACATTTCAAAGAG CCGATTCAAGTGTCAGGAAGATGGAAAGAACTGTGGGATAAGATGGCTGGGAACATTTCAAAGAG A G NAA20 Ensembl:ENSG00000173418 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs996744519 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571404,Human_RBP_ID_22599920 Human_Splice_Rec_2064978,Human_Splice_Rec_2064979 RMVar_hsa_circ_208962,RMVar_hsa_circ_127399 49267 RMVar_ID_49267 Human_SNP_ID_676009927 A-to-I Human chr20 + 20019049 20019049 20019049 CTGGAGCCTCTGGAGAGGCTCACCCTCTCTTTAAAGTGTTCCCAGCCATCTCATCCCATAGTCCT CTGGAGCCTCTGGAGAGGCTCACCCTCTCTTTGAAGTGTTCCCAGCCATCTCATCCCATAGTCCT A G NAA20 Ensembl:ENSG00000173418 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1404954323 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_208962,RMVar_hsa_circ_127399 49268 RMVar_ID_49268 Human_SNP_ID_676009948 A-to-I Human chr20 + 20019151 20019151 20019151 TTTTCGTTTTCACTTACTGCCCTGTTGTTTTTAAAAGTGGATCTAGGATTGATAGGTGGGCAGAG TTTTCGTTTTCACTTACTGCCCTGTTGTTTTTCAAAGTGGATCTAGGATTGATAGGTGGGCAGAG A C NAA20 Ensembl:ENSG00000173418 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1320892401 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571405 RMVar_hsa_circ_208962,RMVar_hsa_circ_127399 49269 RMVar_ID_49269 Human_SNP_ID_676011426 A-to-I Human chr20 + 20025718 20025718 20025718 CCTTTCTACCTACAATACCTCGCCCACTGGCCAGAGTATTTCATTGTTGCAGAGGCACCTGGTGG CCTTTCTACCTACAATACCTCGCCCACTGGCCGGAGTATTTCATTGTTGCAGAGGCACCTGGTGG A G NAA20 Ensembl:ENSG00000173418 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs375943130 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_559956,Human_RBP_ID_2678753,Human_RBP_ID_4661292,Human_RBP_ID_6982992,Human_RBP_ID_17968115,Human_RBP_ID_18769221,Human_RBP_ID_25626837,Human_RBP_ID_26820713 Human_Splice_Rec_2064982,Human_Splice_Rec_2064983,Human_Splice_Rec_2064992,Human_Splice_Rec_2064993,Human_Splice_Rec_2065000,Human_Splice_Rec_2065001,Human_Splice_Rec_2065008,Human_Splice_Rec_2065009,Human_Splice_Rec_2065018,Human_Splice_Rec_2065019,Human_Splice_Rec_2065028,Human_Splice_Rec_2065029 Human_miRNA_ID_2784771 RMVar_hsa_circ_72024,RMVar_hsa_circ_208962,RMVar_hsa_circ_127399,RMVar_hsa_circ_337041,RMVar_hsa_circ_208965,RMVar_hsa_circ_76570,RMVar_hsa_circ_326044,RMVar_hsa_circ_86982,RMVar_hsa_circ_208966 49270 RMVar_ID_49270 Human_SNP_ID_676013967 A-to-I Human chr20 - 20035361 20035361 20035361 GCTATGAAAAATGATGTCCCATGTTCACATAAATTTGGGAAATTCTGGACTAAGACTTAAGTCTC GCTATGAAAAATGATGTCCCATGTTCACATAAGTTTGGGAAATTCTGGACTAAGACTTAAGTCTC T C CRNKL1 Ensembl:ENSG00000101343 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs753432900 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8529122,Human_RBP_ID_17510749,Human_RBP_ID_17968148 49271 RMVar_ID_49271 Human_SNP_ID_676148877 A-to-I Human chr20 - 20594796 20594796 20594796 TGAACTTGGGAGGTGGAGCTTGCAGTGAGTCAAGATCACGCCATTGTGCTCCAGCCTGGCCGACA TGAACTTGGGAGGTGGAGCTTGCAGTGAGTCAGGATCACGCCATTGTGCTCCAGCCTGGCCGACA T C RALGAPA2 Ensembl:ENSG00000188559 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1279577307 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_208985,RMVar_hsa_circ_331825,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_331106,RMVar_hsa_circ_66594,RMVar_hsa_circ_48998,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_356049,RMVar_hsa_circ_360395,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 49272 RMVar_ID_49272 Human_SNP_ID_676299034 A-to-I Human chr20 + 21208609 21208609 21208609 CCTGTAGTCCCAGCTACTTAGGAGGCTGAGGCAGGAGAATGGCCTGAACCCAGGAGGCGGAGCTT CCTGTAGTCCCAGCTACTTAGGAGGCTGAGGCTGGAGAATGGCCTGAACCCAGGAGGCGGAGCTT A T KIZ Ensembl:ENSG00000088970 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1466670041 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24781,RMVar_hsa_circ_74373 49273 RMVar_ID_49273 Human_SNP_ID_676303772 A-to-I Human chr20 + 21229678 21229678 21229678 CTTACTGAAGCCTCAACCTACCAATCTCAAGCAATCTTCCCTCCTCAGCCTCCCAAGTAGCTGGG CTTACTGAAGCCTCAACCTACCAATCTCAAGCCATCTTCCCTCCTCAGCCTCCCAAGTAGCTGGG A C KIZ Ensembl:ENSG00000088970 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1482250103 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19238,RMVar_hsa_circ_74373,RMVar_hsa_circ_337687,RMVar_hsa_circ_209024 49274 RMVar_ID_49274 Human_SNP_ID_676305694 A-to-I Human chr20 + 21237959 21237959 21237959 TCAAGCAACCCTCCCACCTCAGCCTCCCAAGTAGCTGAGACCACAGGCACATGCCACCATGCCTG TCAAGCAACCCTCCCACCTCAGCCTCCCAAGTGGCTGAGACCACAGGCACATGCCACCATGCCTG A G KIZ Ensembl:ENSG00000088970 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1211258127 Functional Loss SNV dbSNP153 33..33 33 - - - 49275 RMVar_ID_49275 Human_SNP_ID_676322146 A-to-I Human chr20 + 21305311 21305311 21305311 ACGGAGTCTCGCTATGTCTCTTAGGCTGGAGTACGGTGGCATGATCTCGGCTCACTACAACCTCT ACGGAGTCTCGCTATGTCTCTTAGGCTGGAGTGCGGTGGCATGATCTCGGCTCACTACAACCTCT A G XRN2 Ensembl:ENSG00000088930 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1171276845 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6983970,Human_RBP_ID_14047816,Human_RBP_ID_18769377 RMVar_hsa_circ_209025,RMVar_hsa_circ_115342 49276 RMVar_ID_49276 Human_SNP_ID_676323731 A-to-I Human chr20 + 21312811 21312811 21312811 GTATTTTTAGTAGAGGTTTCACCACGTTGGCTAAGCTGGTCTTGAACTCCTGACCTCAGGCGATC GTATTTTTAGTAGAGGTTTCACCACGTTGGCTGAGCTGGTCTTGAACTCCTGACCTCAGGCGATC A G XRN2 Ensembl:ENSG00000088930 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs959548598 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14048083 RMVar_hsa_circ_209025,RMVar_hsa_circ_115342 49277 RMVar_ID_49277 Human_SNP_ID_676324398 A-to-I Human chr20 + 21315741 21315741 21315741 GTCTCGAATCAACTCCTGAGCTCAGATGATCCACCTCCCTCAGCCTCCCAAAGTGTTGGGATTAC GTCTCGAATCAACTCCTGAGCTCAGATGATCCCCCTCCCTCAGCCTCCCAAAGTGTTGGGATTAC A C XRN2 Ensembl:ENSG00000088930 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs998637774 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25595875 RMVar_hsa_circ_209025,RMVar_hsa_circ_115342 49278 RMVar_ID_49278 Human_SNP_ID_676336943 A-to-I Human chr20 + 21366256 21366248 21366257 ATATATATTATATATATAAACTTTATGAAAATACTGGGTTTGGGCCGGGCACGGTGGCTCGCTCC ATATATATTATATATATAAACTTTA_________TGGGTTTGGGCCGGGCACGGTGGCTCGCTCC ATGAAAATAC A XRN2 Ensembl:ENSG00000088930 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1378012139 Functional Loss DEL dbSNP153 26..34 33 - - - RMVar_hsa_circ_93034,RMVar_hsa_circ_273020,RMVar_hsa_circ_209027,RMVar_hsa_circ_209026,RMVar_hsa_circ_48448,RMVar_hsa_circ_15219,RMVar_hsa_circ_85823,RMVar_hsa_circ_209038,RMVar_hsa_circ_209041,RMVar_hsa_circ_117092,RMVar_hsa_circ_209046,RMVar_hsa_circ_30235,RMVar_hsa_circ_95093,RMVar_hsa_circ_209050,RMVar_hsa_circ_369995,RMVar_hsa_circ_209054,RMVar_hsa_circ_93138,RMVar_hsa_circ_22677,RMVar_hsa_circ_209055,RMVar_hsa_circ_76580,RMVar_hsa_circ_47820,RMVar_hsa_circ_107087,RMVar_hsa_circ_209060,RMVar_hsa_circ_209061,RMVar_hsa_circ_209063,RMVar_hsa_circ_275670,RMVar_hsa_circ_363114,RMVar_hsa_circ_209064,RMVar_hsa_circ_85800,RMVar_hsa_circ_209066,RMVar_hsa_circ_330034,RMVar_hsa_circ_270727,RMVar_hsa_circ_16895,RMVar_hsa_circ_209067,RMVar_hsa_circ_209068 49279 RMVar_ID_49279 Human_SNP_ID_676336945 A-to-I Human chr20 + 21366256 21366256 21366256 ATATATATTATATATATAAACTTTATGAAAATACTGGGTTTGGGCCGGGCACGGTGGCTCGCTCC ATATATATTATATATATAAACTTTATGAAAATGCTGGGTTTGGGCCGGGCACGGTGGCTCGCTCC A G XRN2 Ensembl:ENSG00000088930 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1282813619 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_93034,RMVar_hsa_circ_273020,RMVar_hsa_circ_209027,RMVar_hsa_circ_209026,RMVar_hsa_circ_48448,RMVar_hsa_circ_15219,RMVar_hsa_circ_85823,RMVar_hsa_circ_209038,RMVar_hsa_circ_209041,RMVar_hsa_circ_117092,RMVar_hsa_circ_209046,RMVar_hsa_circ_30235,RMVar_hsa_circ_95093,RMVar_hsa_circ_209050,RMVar_hsa_circ_369995,RMVar_hsa_circ_209054,RMVar_hsa_circ_93138,RMVar_hsa_circ_22677,RMVar_hsa_circ_209055,RMVar_hsa_circ_76580,RMVar_hsa_circ_47820,RMVar_hsa_circ_107087,RMVar_hsa_circ_209060,RMVar_hsa_circ_209061,RMVar_hsa_circ_209063,RMVar_hsa_circ_275670,RMVar_hsa_circ_363114,RMVar_hsa_circ_209064,RMVar_hsa_circ_85800,RMVar_hsa_circ_209066,RMVar_hsa_circ_330034,RMVar_hsa_circ_270727,RMVar_hsa_circ_16895,RMVar_hsa_circ_209067,RMVar_hsa_circ_209068 49280 RMVar_ID_49280 Human_SNP_ID_676436420 A-to-I Human chr20 - 21755475 21755475 21755475 TCTCAGAGGTGATCGGCGATCAGAGGGCGATGAAGTTCTAGATCCATTGAGACAAGCTCTAGACA TCTCAGAGGTGATCGGCGATCAGAGGGCGATGTAGTTCTAGATCCATTGAGACAAGCTCTAGACA T A - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs948746309 Functional Loss SNV dbSNP153 33..33 33 - - - 49281 RMVar_ID_49281 Human_SNP_ID_676870678 A-to-I Human chr20 + 23368090 23368090 23368090 GAAATTAGCATTTAATGACATGCATTATGACTACAGAATGAGTAGAATTGTTTAAAGAAAGCTTG GAAATTAGCATTTAATGACATGCATTATGACTGCAGAATGAGTAGAATTGTTTAAAGAAAGCTTG A G GZF1 Ensembl:ENSG00000125812 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs561836947 Functional Loss SNV dbSNP153 33..33 33 - - - 49282 RMVar_ID_49282 Human_SNP_ID_676878447 A-to-I Human chr20 - 23398761 23398761 23398761 CGGCTCACTGCAACCTCCGCCTCCCGGATTCAAGCAATTGTCCTACCTCAGCCTCCCAAGTAGCT CGGCTCACTGCAACCTCCGCCTCCCGGATTCATGCAATTGTCCTACCTCAGCCTCCCAAGTAGCT T A NAPB Ensembl:ENSG00000125814 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215938704 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_363538,RMVar_hsa_circ_321837,RMVar_hsa_circ_283391,RMVar_hsa_circ_209077,RMVar_hsa_circ_315079,RMVar_hsa_circ_60846 49283 RMVar_ID_49283 Human_SNP_ID_677371901 A-to-I Human chr20 + 25209333 25209333 25209333 GGGGTTTCACCATATTCGCCAGGATGGTCTCGAACTCCTGACCTCGTGATCTGCTCACCTTGGCC GGGGTTTCACCATATTCGCCAGGATGGTCTCGGACTCCTGACCTCGTGATCTGCTCACCTTGGCC A G ENTPD6 Ensembl:ENSG00000197586 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs961749789 Functional Loss SNV dbSNP153 33..33 33 - - - 49284 RMVar_ID_49284 Human_SNP_ID_677377118 A-to-I Human chr20 + 25228814 25228814 25228814 AAAAAAAAAGCCGGGCATAGTGGTAGGCTTCTATAATCCCAGCTACTAGGGAGGCTGAGGTACGA AAAAAAAAAGCCGGGCATAGTGGTAGGCTTCTGTAATCCCAGCTACTAGGGAGGCTGAGGTACGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956349663 Functional Loss SNV dbSNP153 33..33 33 - - - 49285 RMVar_ID_49285 Human_SNP_ID_677380735 A-to-I Human chr20 - 25242908 25242908 25242908 CTCCCACCCCAGCCTCCCAAGTAGTTGGAACTACAGGTGCATGCCACCACGCCCAGCTAATTTTT CTCCCACCCCAGCCTCCCAAGTAGTTGGAACTGCAGGTGCATGCCACCACGCCCAGCTAATTTTT T C AL121772.1 Ensembl:ENSG00000274414 lincRNA intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs889504219 Functional Loss SNV dbSNP153 33..33 33 - - - 49286 RMVar_ID_49286 Human_SNP_ID_677387097 A-to-I Human chr20 + 25265475 25265475 25265475 TTATAGTTTTTATTTGCATGTTCCTGATAACTAATGATGCTGAGCATCTTTTCACGTGCTTGTGG TTATAGTTTTTATTTGCATGTTCCTGATAACTGATGATGCTGAGCATCTTTTCACGTGCTTGTGG A G PYGB Ensembl:ENSG00000100994 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1319348662 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20476,RMVar_hsa_circ_84952,RMVar_hsa_circ_209110,RMVar_hsa_circ_120697,RMVar_hsa_circ_209111 49287 RMVar_ID_49287 Human_SNP_ID_677399693 A-to-I Human chr20 - 25304673 25304673 25304673 GTCCCAGCTACTCGGGAGGCTGAAGCAGGAGAATCACTTGAACCCAGGAGGCAGAGGTTGCAGTG GTCCCAGCTACTCGGGAGGCTGAAGCAGGAGAGTCACTTGAACCCAGGAGGCAGAGGTTGCAGTG T C ABHD12 Ensembl:ENSG00000100997 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs900818098 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_304315,RMVar_hsa_circ_333662,RMVar_hsa_circ_124611,RMVar_hsa_circ_209135,RMVar_hsa_circ_209136,RMVar_hsa_circ_209137,RMVar_hsa_circ_209138,RMVar_hsa_circ_77639,RMVar_hsa_circ_79803,RMVar_hsa_circ_298022,RMVar_hsa_circ_209139,RMVar_hsa_circ_209140 49288 RMVar_ID_49288 Human_SNP_ID_677399697 A-to-I Human chr20 - 25304682 25304682 25304682 ACGCCTGTAGTCCCAGCTACTCGGGAGGCTGAAGCAGGAGAATCACTTGAACCCAGGAGGCAGAG ACGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCCAGGAGGCAGAG T C ABHD12 Ensembl:ENSG00000100997 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1568712123 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_304315,RMVar_hsa_circ_333662,RMVar_hsa_circ_124611,RMVar_hsa_circ_209135,RMVar_hsa_circ_209136,RMVar_hsa_circ_209137,RMVar_hsa_circ_209138,RMVar_hsa_circ_77639,RMVar_hsa_circ_79803,RMVar_hsa_circ_298022,RMVar_hsa_circ_209139,RMVar_hsa_circ_209140 49289 RMVar_ID_49289 Human_SNP_ID_677402285 A-to-I Human chr20 - 25313730 25313730 25313730 GTCACCCAGCTGGATTGCAGTGATGTGATCTCAGCTCACTGCAACCTCTGCCTCCCGGGTTCAAG GTCACCCAGCTGGATTGCAGTGATGTGATCTCGGCTCACTGCAACCTCTGCCTCCCGGGTTCAAG T C ABHD12 Ensembl:ENSG00000100997 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1373291471 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115818,RMVar_hsa_circ_333662,RMVar_hsa_circ_209137,RMVar_hsa_circ_17377,RMVar_hsa_circ_77639,RMVar_hsa_circ_79803,RMVar_hsa_circ_209139,RMVar_hsa_circ_209140,RMVar_hsa_circ_302577,RMVar_hsa_circ_345369,RMVar_hsa_circ_22666,RMVar_hsa_circ_209143,RMVar_hsa_circ_329945,RMVar_hsa_circ_209144,RMVar_hsa_circ_209146 49290 RMVar_ID_49290 Human_SNP_ID_677402294 A-to-I Human chr20 - 25313767 25313763 25313767 TTGGTTTTGGTTTTGCTTTGAGACAGGGTCTCACTCTGTCACCCAGCTGGATTGCAGTGATGTGA TTGGTTTTGGTTTTGCTTTGAGACAGGGTCTC____TGTCACCCAGCTGGATTGCAGTGATGTGA AGAGT A ABHD12 Ensembl:ENSG00000100997 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs954785534 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_115818,RMVar_hsa_circ_333662,RMVar_hsa_circ_209137,RMVar_hsa_circ_17377,RMVar_hsa_circ_77639,RMVar_hsa_circ_79803,RMVar_hsa_circ_209139,RMVar_hsa_circ_209140,RMVar_hsa_circ_302577,RMVar_hsa_circ_345369,RMVar_hsa_circ_22666,RMVar_hsa_circ_209143,RMVar_hsa_circ_329945,RMVar_hsa_circ_209144,RMVar_hsa_circ_209146 49291 RMVar_ID_49291 Human_SNP_ID_677402467 A-to-I Human chr20 - 25314475 25314475 25314475 TGGGGTATCGCTGTGTTGCCTAGGCTAGTCTCAGACTCCTGGCCTCAAGCGATCCTCCTGCCTCA TGGGGTATCGCTGTGTTGCCTAGGCTAGTCTCGGACTCCTGGCCTCAAGCGATCCTCCTGCCTCA T C ABHD12 Ensembl:ENSG00000100997 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs887245044 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571413 RMVar_hsa_circ_115818,RMVar_hsa_circ_333662,RMVar_hsa_circ_209137,RMVar_hsa_circ_17377,RMVar_hsa_circ_77639,RMVar_hsa_circ_79803,RMVar_hsa_circ_209139,RMVar_hsa_circ_209140,RMVar_hsa_circ_302577,RMVar_hsa_circ_345369,RMVar_hsa_circ_22666,RMVar_hsa_circ_209143,RMVar_hsa_circ_329945,RMVar_hsa_circ_209144,RMVar_hsa_circ_209146 49292 RMVar_ID_49292 Human_SNP_ID_677402513 A-to-I Human chr20 - 25314643 25314636 25314644 ATAGGATCTCACTTTGTCACCCAACCTGGAGTACAGTAGCATGATTGTAGCTCACTGCAGCCTTG ATAGGATCTCACTTTGTCACCCAACCTGGAG________CATGATTGTAGCTCACTGCAGCCTTG GCTACTGTA G ABHD12 Ensembl:ENSG00000100997 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1416029670 Functional Loss DEL dbSNP153 32..39 33 - - - RMVar_hsa_circ_115818,RMVar_hsa_circ_333662,RMVar_hsa_circ_209137,RMVar_hsa_circ_17377,RMVar_hsa_circ_77639,RMVar_hsa_circ_79803,RMVar_hsa_circ_209139,RMVar_hsa_circ_209140,RMVar_hsa_circ_302577,RMVar_hsa_circ_345369,RMVar_hsa_circ_22666,RMVar_hsa_circ_209143,RMVar_hsa_circ_329945,RMVar_hsa_circ_209144,RMVar_hsa_circ_209146 49293 RMVar_ID_49293 Human_SNP_ID_677417938 A-to-I Human chr20 - 25374040 25374040 25374040 GCATGCCTTTGATTACAACTAATTGGGAGGCTAAGGTGGGAGGATTGCTTGAGCCTGGGAGGTCA GCATGCCTTTGATTACAACTAATTGGGAGGCTGAGGTGGGAGGATTGCTTGAGCCTGGGAGGTCA T C ABHD12 Ensembl:ENSG00000100997 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs986826851 Functional Loss SNV dbSNP153 33..33 33 - - - 49294 RMVar_ID_49294 Human_SNP_ID_677417969 A-to-I Human chr20 - 25374163 25374163 25374163 CTAGCACTTTGGGAGGATAAAGAAGGAGGATCACTTGAGCCCAGGAATCTGAGACCAGCCTGGGC CTAGCACTTTGGGAGGATAAAGAAGGAGGATCTCTTGAGCCCAGGAATCTGAGACCAGCCTGGGC T A ABHD12 Ensembl:ENSG00000100997 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1158474583 Functional Loss SNV dbSNP153 33..33 33 - - - 49295 RMVar_ID_49295 Human_SNP_ID_677417970 A-to-I Human chr20 - 25374163 25374163 25374163 CTAGCACTTTGGGAGGATAAAGAAGGAGGATCACTTGAGCCCAGGAATCTGAGACCAGCCTGGGC CTAGCACTTTGGGAGGATAAAGAAGGAGGATCGCTTGAGCCCAGGAATCTGAGACCAGCCTGGGC T C ABHD12 Ensembl:ENSG00000100997 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1158474583 Functional Loss SNV dbSNP153 33..33 33 - - - 49296 RMVar_ID_49296 Human_SNP_ID_677417974 A-to-I Human chr20 - 25374172 25374170 25374173 CCTGTAATCCTAGCACTTTGGGAGGATAAAGAAGGAGGATCACTTGAGCCCAGGAATCTGAGACC CCTGTAATCCTAGCACTTTGGGAGGATAAAG___GAGGATCACTTGAGCCCAGGAATCTGAGACC CCTT C ABHD12 Ensembl:ENSG00000100997 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1192014845 Functional Loss DEL dbSNP153 32..34 33 - - - 49297 RMVar_ID_49297 Human_SNP_ID_677428287 A-to-I Human chr20 + 25410220 25410220 25410220 AAAATTAGCCAGGCGTGGTGGGATGTGCCTGTAGTCCCAGCTACTCGGAAGGCTGAGGCAGGAGA AAAATTAGCCAGGCGTGGTGGGATGTGCCTGTTGTCCCAGCTACTCGGAAGGCTGAGGCAGGAGA A T GINS1 Ensembl:ENSG00000101003 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1275428885 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110169,RMVar_hsa_circ_209153 49298 RMVar_ID_49298 Human_SNP_ID_677428426 A-to-I Human chr20 + 25410703 25410703 25410703 CCTGCCTCAGCTTCCCTAGTAGCTGGGATTACAGGCGCCTGCCACCATGCCCAGATAATTTTATG CCTGCCTCAGCTTCCCTAGTAGCTGGGATTACGGGCGCCTGCCACCATGCCCAGATAATTTTATG A G GINS1 Ensembl:ENSG00000101003 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1305006323 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110169,RMVar_hsa_circ_209153 49299 RMVar_ID_49299 Human_SNP_ID_677428437 A-to-I Human chr20 + 25410733 25410733 25410733 ACAGGCGCCTGCCACCATGCCCAGATAATTTTATGTATTTTTAGTAGAGATGGGGTTTCACTATT ACAGGCGCCTGCCACCATGCCCAGATAATTTTGTGTATTTTTAGTAGAGATGGGGTTTCACTATT A G GINS1 Ensembl:ENSG00000101003 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs989495214 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110169,RMVar_hsa_circ_209153 49300 RMVar_ID_49300 Human_SNP_ID_677428550 A-to-I Human chr20 + 25411154 25411154 25411154 AGAATTAGCTGGGTGTGGTGGCACACACCTGTAGTCCCAGCAACTTAGGAGGCTGAAGTGAGAGG AGAATTAGCTGGGTGTGGTGGCACACACCTGTGGTCCCAGCAACTTAGGAGGCTGAAGTGAGAGG A G GINS1 Ensembl:ENSG00000101003 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs1048039203 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14053760 Human_Splice_Rec_2068110 RMVar_hsa_circ_110169,RMVar_hsa_circ_209153 49301 RMVar_ID_49301 Human_SNP_ID_677428713 A-to-I Human chr20 + 25411778 25411778 25411778 CAACCTGGTGAACATGGTGAAACCCTGTCTCTACTAAAAATACAAAAATTAGCTGGACGTGATGG CAACCTGGTGAACATGGTGAAACCCTGTCTCTGCTAAAAATACAAAAATTAGCTGGACGTGATGG A G GINS1 Ensembl:ENSG00000101003 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs373120649 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110169,RMVar_hsa_circ_209153 49302 RMVar_ID_49302 Human_SNP_ID_677429099 A-to-I Human chr20 + 25413229 25413229 25413229 TGTCACCACGCCTGGCTAATTTTTGTATATTTAGGAGAGACGGGGTTTCACCATGTTGACCAGGC TGTCACCACGCCTGGCTAATTTTTGTATATTTCGGAGAGACGGGGTTTCACCATGTTGACCAGGC A C GINS1 Ensembl:ENSG00000101003 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1297274810 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110169,RMVar_hsa_circ_209153 49303 RMVar_ID_49303 Human_SNP_ID_677429100 A-to-I Human chr20 + 25413229 25413229 25413229 TGTCACCACGCCTGGCTAATTTTTGTATATTTAGGAGAGACGGGGTTTCACCATGTTGACCAGGC TGTCACCACGCCTGGCTAATTTTTGTATATTTGGGAGAGACGGGGTTTCACCATGTTGACCAGGC A G GINS1 Ensembl:ENSG00000101003 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1297274810 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110169,RMVar_hsa_circ_209153 49304 RMVar_ID_49304 Human_SNP_ID_677430986 A-to-I Human chr20 + 25420626 25420626 25420626 ACATGGTGAAACCCTGTTTCTACTAAAAATACAAAGATTAGCTGGGTGTGGTGGTGTGCACCTGT ACATGGTGAAACCCTGTTTCTACTAAAAATACGAAGATTAGCTGGGTGTGGTGGTGTGCACCTGT A G GINS1 Ensembl:ENSG00000101003 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs528879007 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_297852,RMVar_hsa_circ_110169,RMVar_hsa_circ_209153,RMVar_hsa_circ_333390,RMVar_hsa_circ_209156,RMVar_hsa_circ_209157,RMVar_hsa_circ_107878,RMVar_hsa_circ_311312,RMVar_hsa_circ_286828,RMVar_hsa_circ_209158,RMVar_hsa_circ_209160,RMVar_hsa_circ_283878,RMVar_hsa_circ_340237,RMVar_hsa_circ_209159 49305 RMVar_ID_49305 Human_SNP_ID_677430987 A-to-I Human chr20 + 25420633 25420633 25420633 GAAACCCTGTTTCTACTAAAAATACAAAGATTAGCTGGGTGTGGTGGTGTGCACCTGTAATCCCA GAAACCCTGTTTCTACTAAAAATACAAAGATTGGCTGGGTGTGGTGGTGTGCACCTGTAATCCCA A G GINS1 Ensembl:ENSG00000101003 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1266320253 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_297852,RMVar_hsa_circ_110169,RMVar_hsa_circ_209153,RMVar_hsa_circ_333390,RMVar_hsa_circ_209156,RMVar_hsa_circ_209157,RMVar_hsa_circ_107878,RMVar_hsa_circ_311312,RMVar_hsa_circ_286828,RMVar_hsa_circ_209158,RMVar_hsa_circ_209160,RMVar_hsa_circ_283878,RMVar_hsa_circ_340237,RMVar_hsa_circ_209159 49306 RMVar_ID_49306 Human_SNP_ID_677437612 A-to-I Human chr20 + 25446235 25446235 25446235 TTTTGGTTTTGTTTTGTAGAGACTGTCTCACTATGTTGCCCAAGCTGGTCTCAAACTCCTGGCCT TTTTGGTTTTGTTTTGTAGAGACTGTCTCACTGTGTTGCCCAAGCTGGTCTCAAACTCCTGGCCT A G GINS1 Ensembl:ENSG00000101003 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs781012901 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_560529,Human_RBP_ID_1927123,Human_RBP_ID_3645038,Human_RBP_ID_6986301,Human_RBP_ID_14054410,Human_RBP_ID_23897700,Human_RBP_ID_27700446 Human_miRNA_ID_1141643 RMVar_hsa_circ_110169,RMVar_hsa_circ_209153,RMVar_hsa_circ_209157,RMVar_hsa_circ_107878 49307 RMVar_ID_49307 Human_SNP_ID_677437613 A-to-I Human chr20 + 25446235 25446235 25446235 TTTTGGTTTTGTTTTGTAGAGACTGTCTCACTATGTTGCCCAAGCTGGTCTCAAACTCCTGGCCT TTTTGGTTTTGTTTTGTAGAGACTGTCTCACTTTGTTGCCCAAGCTGGTCTCAAACTCCTGGCCT A T GINS1 Ensembl:ENSG00000101003 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs781012901 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_560529,Human_RBP_ID_1927123,Human_RBP_ID_3645038,Human_RBP_ID_6986301,Human_RBP_ID_14054410,Human_RBP_ID_23897700,Human_RBP_ID_27700446 Human_miRNA_ID_1141643 RMVar_hsa_circ_110169,RMVar_hsa_circ_209153,RMVar_hsa_circ_209157,RMVar_hsa_circ_107878 49308 RMVar_ID_49308 Human_SNP_ID_677437632 A-to-I Human chr20 + 25446296 25446296 25446296 GCCTCAAGCAGTCCTCCCACCTTAGCTTCTCAAAGTGTTGAGATCACAGGCGTGAGCCACTGCAC GCCTCAAGCAGTCCTCCCACCTTAGCTTCTCACAGTGTTGAGATCACAGGCGTGAGCCACTGCAC A C GINS1 Ensembl:ENSG00000101003 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1014280058 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14054419,Human_RBP_ID_23897701 RMVar_hsa_circ_110169,RMVar_hsa_circ_209153,RMVar_hsa_circ_209157,RMVar_hsa_circ_107878 49309 RMVar_ID_49309 Human_SNP_ID_677437634 A-to-I Human chr20 + 25446304 25446304 25446304 CAGTCCTCCCACCTTAGCTTCTCAAAGTGTTGAGATCACAGGCGTGAGCCACTGCACCCGGCCCC CAGTCCTCCCACCTTAGCTTCTCAAAGTGTTGGGATCACAGGCGTGAGCCACTGCACCCGGCCCC A G GINS1 Ensembl:ENSG00000101003 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs556157880 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14054419,Human_RBP_ID_17394830 Human_miRNA_ID_1224983,Human_miRNA_ID_1529275,Human_miRNA_ID_1537302 RMVar_hsa_circ_110169,RMVar_hsa_circ_209153,RMVar_hsa_circ_209157,RMVar_hsa_circ_107878 49310 RMVar_ID_49310 Human_SNP_ID_677437812 A-to-I Human chr20 + 25447119 25447119 25447119 TGGGGTGCAGTGGCGTGATCTTGGCTCACTGCAATCTCTATCCCCTGGGTTCAAGTGATTCTCTT TGGGGTGCAGTGGCGTGATCTTGGCTCACTGCGATCTCTATCCCCTGGGTTCAAGTGATTCTCTT A G GINS1 Ensembl:ENSG00000101003 Protein coding 3'UTR GSE38233;GSE100210;GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,29129909,32596459 RNA-Seq:(High) rs981138661 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6986358,Human_RBP_ID_14054470,Human_RBP_ID_17280795,Human_RBP_ID_17510853,Human_RBP_ID_17968795 Human_miRNA_ID_685728,Human_miRNA_ID_888273,Human_miRNA_ID_1064914,Human_miRNA_ID_1076228 RMVar_hsa_circ_110169,RMVar_hsa_circ_209153,RMVar_hsa_circ_209157,RMVar_hsa_circ_107878 49311 RMVar_ID_49311 Human_SNP_ID_677437849 A-to-I Human chr20 + 25447260 25447260 25447260 CAGAGTTTTACCATGTTGGCCAGGCTGGTTTCAAACTCCTGACCTCAAGTGACCCACCTTGGCCT CAGAGTTTTACCATGTTGGCCAGGCTGGTTTCGAACTCCTGACCTCAAGTGACCCACCTTGGCCT A G GINS1 Ensembl:ENSG00000101003 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1457224290 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_560549,Human_RBP_ID_6986363,Human_RBP_ID_14054473 RMVar_hsa_circ_110169,RMVar_hsa_circ_209153,RMVar_hsa_circ_209157,RMVar_hsa_circ_107878 49312 RMVar_ID_49312 Human_SNP_ID_677437857 A-to-I Human chr20 + 25447297 25447297 25447297 CCTGACCTCAAGTGACCCACCTTGGCCTCCCAAAGTTTTGGGATTACAAGTGTGGGCCACCGCGG CCTGACCTCAAGTGACCCACCTTGGCCTCCCAGAGTTTTGGGATTACAAGTGTGGGCCACCGCGG A G GINS1 Ensembl:ENSG00000101003 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1488583271 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_560549,Human_RBP_ID_14054474 Human_miRNA_ID_2033262,Human_miRNA_ID_2888202 RMVar_hsa_circ_110169,RMVar_hsa_circ_209153,RMVar_hsa_circ_209157,RMVar_hsa_circ_107878 49313 RMVar_ID_49313 Human_SNP_ID_677437955 A-to-I Human chr20 + 25447707 25447707 25447707 GTGTTGGCCAGGCTGTGTTGAACTCCTGAGCTAAAGCAATACACTTGCCTCGTCCTCCCCATGTG GTGTTGGCCAGGCTGTGTTGAACTCCTGAGCTTAAGCAATACACTTGCCTCGTCCTCCCCATGTG A T GINS1 Ensembl:ENSG00000101003 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1489142131 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6986390,Human_RBP_ID_14054496,Human_RBP_ID_17510859,Human_RBP_ID_17968801,Human_RBP_ID_18321127,Human_RBP_ID_26489046 Human_miRNA_ID_2050014 RMVar_hsa_circ_110169,RMVar_hsa_circ_209153,RMVar_hsa_circ_209157,RMVar_hsa_circ_107878 49314 RMVar_ID_49314 Human_SNP_ID_677437958 A-to-I Human chr20 + 25447712 25447712 25447712 GGCCAGGCTGTGTTGAACTCCTGAGCTAAAGCAATACACTTGCCTCGTCCTCCCCATGTGCTGGG GGCCAGGCTGTGTTGAACTCCTGAGCTAAAGCGATACACTTGCCTCGTCCTCCCCATGTGCTGGG A G GINS1 Ensembl:ENSG00000101003 Protein coding 3'UTR GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-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 49315 RMVar_ID_49315 Human_SNP_ID_677438029 A-to-I Human chr20 + 25448010 25448010 25448010 AAAATTAGCCAGGTGTGGTGGTGCATGCCTGTAGTCACAGTTACACGGCAGGCTGAGGTGGGAGG AAAATTAGCCAGGTGTGGTGGTGCATGCCTGTCGTCACAGTTACACGGCAGGCTGAGGTGGGAGG A C GINS1 Ensembl:ENSG00000101003 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,31158229,31158229,31158229,32596459,32596459 RNA-Seq:(High) rs1246123064 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110169,RMVar_hsa_circ_209153,RMVar_hsa_circ_209157,RMVar_hsa_circ_107878 49316 RMVar_ID_49316 Human_SNP_ID_677446199 A-to-I Human chr20 - 25476672 25476672 25476672 CCAGGTGATGGCAGAGAGTCTGAGGAGGCGGCAGGAGCCGGGCCTCGCCGCAGGCAAGCCCAGGA CCAGGTGATGGCAGAGAGTCTGAGGAGGCGGCGGGAGCCGGGCCTCGCCGCAGGCAAGCCCAGGA T C NINL Ensembl:ENSG00000101004 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1202059549 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9390233 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 49317 RMVar_ID_49317 Human_SNP_ID_677470323 A-to-I Human chr20 - 25568906 25568906 25568906 AAAATATTTTGTAGAGACAGGGAGGGGTCTCAATGTGTTGCCCAGGCTGGTCTCAAACTCCTGGC AAAATATTTTGTAGAGACAGGGAGGGGTCTCATTGTGTTGCCCAGGCTGGTCTCAAACTCCTGGC T A NINL Ensembl:ENSG00000101004 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560177372 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571430 49318 RMVar_ID_49318 Human_SNP_ID_677470324 A-to-I Human chr20 - 25568906 25568906 25568906 AAAATATTTTGTAGAGACAGGGAGGGGTCTCAATGTGTTGCCCAGGCTGGTCTCAAACTCCTGGC AAAATATTTTGTAGAGACAGGGAGGGGTCTCAGTGTGTTGCCCAGGCTGGTCTCAAACTCCTGGC T C NINL Ensembl:ENSG00000101004 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560177372 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571430 49319 RMVar_ID_49319 Human_SNP_ID_677470325 A-to-I Human chr20 - 25568906 25568906 25568906 AAAATATTTTGTAGAGACAGGGAGGGGTCTCAATGTGTTGCCCAGGCTGGTCTCAAACTCCTGGC AAAATATTTTGTAGAGACAGGGAGGGGTCTCACTGTGTTGCCCAGGCTGGTCTCAAACTCCTGGC T G NINL Ensembl:ENSG00000101004 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560177372 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571430 49320 RMVar_ID_49320 Human_SNP_ID_677472324 A-to-I Human chr20 - 25576727 25576727 25576727 GCTGGCACGGTGGCACATGCATGTAATCCCAGAACTTTGGGAGGCTGAGGTGAGAGGATCTCTTG GCTGGCACGGTGGCACATGCATGTAATCCCAGCACTTTGGGAGGCTGAGGTGAGAGGATCTCTTG T G NINL Ensembl:ENSG00000101004 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1228431047 Functional Loss SNV dbSNP153 33..33 33 - - - 49321 RMVar_ID_49321 Human_SNP_ID_677472638 A-to-I Human chr20 - 25577938 25577938 25577938 ATCCCAGCTACTCCATAGGCTGAGGCAGGAGAATCTCTTGAACCTGCGAGGTGGAGATTGCAGTG ATCCCAGCTACTCCATAGGCTGAGGCAGGAGACTCTCTTGAACCTGCGAGGTGGAGATTGCAGTG T G NINL Ensembl:ENSG00000101004 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1292204930 Functional Loss SNV dbSNP153 33..33 33 - - - 49322 RMVar_ID_49322 Human_SNP_ID_677472639 A-to-I Human chr20 - 25577944 25577944 25577944 CCTGTAATCCCAGCTACTCCATAGGCTGAGGCAGGAGAATCTCTTGAACCTGCGAGGTGGAGATT CCTGTAATCCCAGCTACTCCATAGGCTGAGGCGGGAGAATCTCTTGAACCTGCGAGGTGGAGATT T C NINL Ensembl:ENSG00000101004 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs888005914 Functional Loss SNV dbSNP153 33..33 33 - - - 49323 RMVar_ID_49323 Human_SNP_ID_677496866 A-to-I Human chr20 + 25677761 25677761 25677761 TTTTGTAGAGATGGGATTTCGCCATGTTGTCCAGGCTGGTCTCAAATTCTTGAGCTCAAGCAATC TTTTGTAGAGATGGGATTTCGCCATGTTGTCCGGGCTGGTCTCAAATTCTTGAGCTCAAGCAATC A G ZNF337-AS1 Ensembl:ENSG00000213742 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs561725446 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119360,RMVar_hsa_circ_209176,RMVar_hsa_circ_209177 49324 RMVar_ID_49324 Human_SNP_ID_677497075 A-to-I Human chr20 + 25678723 25678723 25678723 ATCCCAGTGCTCTGAGAGACTGTGGCAGGCGGATTGCTTGAGGCTAGGAGTTCGAGTCCAGCCTG ATCCCAGTGCTCTGAGAGACTGTGGCAGGCGGGTTGCTTGAGGCTAGGAGTTCGAGTCCAGCCTG A G ZNF337-AS1 Ensembl:ENSG00000213742 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs919407547 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_209177 49325 RMVar_ID_49325 Human_SNP_ID_677497078 A-to-I Human chr20 + 25678736 25678736 25678736 GAGAGACTGTGGCAGGCGGATTGCTTGAGGCTAGGAGTTCGAGTCCAGCCTGGGCAACACGATGA GAGAGACTGTGGCAGGCGGATTGCTTGAGGCTGGGAGTTCGAGTCCAGCCTGGGCAACACGATGA A G ZNF337-AS1 Ensembl:ENSG00000213742 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1376727553 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_209177 49326 RMVar_ID_49326 Human_SNP_ID_677499958 A-to-I Human chr20 - 25690093 25690093 25690093 TTTGTAGAGATGAGCCTTTGCCATGTTGCCCAAACTGGTCCCGAACTCCTGGGATCAAGCGATCC TTTGTAGAGATGAGCCTTTGCCATGTTGCCCAGACTGGTCCCGAACTCCTGGGATCAAGCGATCC T C ZNF337 Ensembl:ENSG00000130684 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,frontal_cortex - 29129909,30559470 RNA-Seq:(High) rs1276431489 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14055592 RMVar_hsa_circ_82957,RMVar_hsa_circ_209180,RMVar_hsa_circ_111563,RMVar_hsa_circ_209182 49327 RMVar_ID_49327 Human_SNP_ID_677500606 A-to-I Human chr20 - 25693187 25693187 25693187 CTGTAATCCCAACTACTCTGGAGCCTGAAGCAAGATAATCGCTTGAATCCAGGAGATGGAGGTTG CTGTAATCCCAACTACTCTGGAGCCTGAAGCAGGATAATCGCTTGAATCCAGGAGATGGAGGTTG T C ZNF337 Ensembl:ENSG00000130684 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1286131414 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14055722 RMVar_hsa_circ_82957,RMVar_hsa_circ_209180,RMVar_hsa_circ_111563,RMVar_hsa_circ_209182 49328 RMVar_ID_49328 Human_SNP_ID_677500611 A-to-I Human chr20 - 25693214 25693214 25693214 AAATTAGCCAGGCATGGTGGCTCACGCCTGTAATCCCAACTACTCTGGAGCCTGAAGCAAGATAA AAATTAGCCAGGCATGGTGGCTCACGCCTGTAGTCCCAACTACTCTGGAGCCTGAAGCAAGATAA T C ZNF337 Ensembl:ENSG00000130684 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1410583842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2679834,Human_RBP_ID_14055722 RMVar_hsa_circ_82957,RMVar_hsa_circ_209180,RMVar_hsa_circ_111563,RMVar_hsa_circ_209182 49329 RMVar_ID_49329 Human_SNP_ID_677500637 A-to-I Human chr20 - 25693319 25693319 25693319 TAATCCCAGCACTTTGGGAGGCCAAGGCGGGCAGATTACCTGAGGCCAGGAGTTCGAGACCAGCC TAATCCCAGCACTTTGGGAGGCCAAGGCGGGCGGATTACCTGAGGCCAGGAGTTCGAGACCAGCC T C ZNF337 Ensembl:ENSG00000130684 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs991267093 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82957,RMVar_hsa_circ_209180,RMVar_hsa_circ_111563,RMVar_hsa_circ_209182 49330 RMVar_ID_49330 Human_SNP_ID_677501041 A-to-I Human chr20 - 25695041 25695041 25695041 GTCTTGACTTCCTGACCTCAGGTGATCCACCCACCTCTACCTCCCAAAGTGCTGGGATTACAGGC GTCTTGACTTCCTGACCTCAGGTGATCCACCCGCCTCTACCTCCCAAAGTGCTGGGATTACAGGC T C ZNF337 Ensembl:ENSG00000130684 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1282706288 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82957,RMVar_hsa_circ_209180,RMVar_hsa_circ_111563,RMVar_hsa_circ_209182 49331 RMVar_ID_49331 Human_SNP_ID_677521246 A-to-I Human chr20 - 25772898 25772898 25772898 GGCCCCAGGTTCCAGGTAGACACTAGAATCCAAATCAACACCAGGCCCCAGATGGACACCCAGGC GGCCCCAGGTTCCAGGTAGACACTAGAATCCAGATCAACACCAGGCCCCAGATGGACACCCAGGC T C FAM182B Ensembl:ENSG00000175170 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1307733678 Functional Loss SNV dbSNP153 33..33 33 - - - 49332 RMVar_ID_49332 Human_SNP_ID_677521247 A-to-I Human chr20 - 25772898 25772898 25772898 GGCCCCAGGTTCCAGGTAGACACTAGAATCCAAATCAACACCAGGCCCCAGATGGACACCCAGGC GGCCCCAGGTTCCAGGTAGACACTAGAATCCACATCAACACCAGGCCCCAGATGGACACCCAGGC T G FAM182B Ensembl:ENSG00000175170 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1307733678 Functional Loss SNV dbSNP153 33..33 33 - - - 49333 RMVar_ID_49333 Human_SNP_ID_677577735 A-to-I Human chr20 + 26017437 26017437 26017437 CACCATGCACAGCTAATTTTTGTATTTTTAGTAGAGTCAGAGATTCACCATGTTGTCCAGGATGG CACCATGCACAGCTAATTTTTGTATTTTTAGTGGAGTCAGAGATTCACCATGTTGTCCAGGATGG A G FAM182A Ensembl:ENSG00000125804 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1476217745 Functional Loss SNV dbSNP153 33..33 33 - - - 49334 RMVar_ID_49334 Human_SNP_ID_678492399 A-to-I Human chr20 - 30396951 30396951 30396951 CTGTAGGTCTAAAAGGAAAAGCATACATACACATAATTGATTTCACATTGTTTTACATTTCCTTT CTGTAGGTCTAAAAGGAAAAGCATACATACACTTAATTGATTTCACATTGTTTTACATTTCCTTT T A - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1252332795 Functional Loss SNV dbSNP153 33..33 33 - - - 49335 RMVar_ID_49335 Human_SNP_ID_678495930 A-to-I Human chr20 + 30404754 30404754 30404754 TGGAAAGTGAGGAGCGTCTCTGCCCAGCCGCCATCCCATCTAGGAAGTGAGGAGCGTCTCTGCCC TGGAAAGTGAGGAGCGTCTCTGCCCAGCCGCCGTCCCATCTAGGAAGTGAGGAGCGTCTCTGCCC A G lnc-DEFB115-4,lnc-DEFB115-3,lnc-DEFB115-5,lnc-DEFB115-4:2 RNACentral:URS00008BE790,RNACentral:URS0000D5D40B,RNACentral:URS00008C33AD,RNACentral:URS00009B5876 lincRNA,lincRNA,lincRNA,lincRNA intron,exon,intron,intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs532953935 Functional Loss SNV dbSNP153 33..33 33 - - - 49336 RMVar_ID_49336 Human_SNP_ID_678746387 A-to-I Human chr20 - 31285759 31285759 31285759 ACCCAGAATCAGTTCCTTGATGAGCTCATGGAACTTGAGATCTTCTTAGCCCAGAGAGCAGTGGA ACCCAGAATCAGTTCCTTGATGAGCTCATGGAGCTTGAGATCTTCTTAGCCCAGAGAGCAGTGGA T C AL121723.1 Ensembl:ENSG00000224628 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878878540 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5594931 Human_miRNA_ID_1886524,Human_miRNA_ID_1886961 49337 RMVar_ID_49337 Human_SNP_ID_678746397 A-to-I Human chr20 - 31285787 31285787 31285787 TGCTCTGACACTTCTTGAATACACTGAGACCCAGAATCAGTTCCTTGATGAGCTCATGGAACTTG TGCTCTGACACTTCTTGAATACACTGAGACCCGGAATCAGTTCCTTGATGAGCTCATGGAACTTG T C AL121723.1 Ensembl:ENSG00000224628 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879252735 Functional Loss SNV dbSNP153 33..33 33 - - - 49338 RMVar_ID_49338 Human_SNP_ID_678811153 A-to-I Human chr20 + 31523168 31523168 31523168 CACCTCCCGGGTTCAAGCAATTCTCCTGCCTCAACCTCCTGAGTAGCTGGGACCATAGGCGCACA CACCTCCCGGGTTCAAGCAATTCTCCTGCCTCCACCTCCTGAGTAGCTGGGACCATAGGCGCACA A C HM13 Ensembl:ENSG00000101294 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1452150651 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_209186,RMVar_hsa_circ_99051 49339 RMVar_ID_49339 Human_SNP_ID_678811777 A-to-I Human chr20 + 31525979 31525979 31525979 GAAACCCCCTCTCTGCAAAAAACACAAAAATTAGCCAGGTATGGTGGCATGTGCCTGTAGTCCCA GAAACCCCCTCTCTGCAAAAAACACAAAAATTGGCCAGGTATGGTGGCATGTGCCTGTAGTCCCA A G HM13 Ensembl:ENSG00000101294 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1286810309 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_209186,RMVar_hsa_circ_99051 49340 RMVar_ID_49340 Human_SNP_ID_678812600 A-to-I Human chr20 + 31529418 31529418 31529418 AAGGCGTGCACCACCACACCTAGCTAATTTTCATATTTTTAGTGGAGATGGGGTTTTGCATGTTG AAGGCGTGCACCACCACACCTAGCTAATTTTCTTATTTTTAGTGGAGATGGGGTTTTGCATGTTG A T HM13 Ensembl:ENSG00000101294 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1027715363 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14057928 RMVar_hsa_circ_26002,RMVar_hsa_circ_209186,RMVar_hsa_circ_99051,RMVar_hsa_circ_350215,RMVar_hsa_circ_369872,RMVar_hsa_circ_209189 49341 RMVar_ID_49341 Human_SNP_ID_678813657 A-to-I Human chr20 + 31533973 31533973 31533973 GCGATTGTAGTTCACAATAACTTTAAACTCCCAGGCTCAGTTAATCTTCCCACCTCAGCCCCCTG GCGATTGTAGTTCACAATAACTTTAAACTCCCGGGCTCAGTTAATCTTCCCACCTCAGCCCCCTG A G HM13 Ensembl:ENSG00000101294 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs776594405 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26002,RMVar_hsa_circ_209186,RMVar_hsa_circ_99051,RMVar_hsa_circ_350215,RMVar_hsa_circ_369872,RMVar_hsa_circ_209189 49342 RMVar_ID_49342 Human_SNP_ID_678813758 A-to-I Human chr20 + 31534417 31534417 31534417 GAGGGGAGGACCCCTGGGCAAGTGCCTTTGTTAGGGCTCAGGGTAGTACAAGCAAAGGGCATGAG GAGGGGAGGACCCCTGGGCAAGTGCCTTTGTTCGGGCTCAGGGTAGTACAAGCAAAGGGCATGAG A C HM13 Ensembl:ENSG00000101294 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1357052662 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_206982,Human_RBP_ID_14058003 RMVar_hsa_circ_26002,RMVar_hsa_circ_209186,RMVar_hsa_circ_99051,RMVar_hsa_circ_350215,RMVar_hsa_circ_369872,RMVar_hsa_circ_209189 49343 RMVar_ID_49343 Human_SNP_ID_678816537 A-to-I Human chr20 + 31546595 31546595 31546595 CATCACGGCGAAACCCCGTCTCTACTAAAAACACAAAAAAAATTAGCCAGGCATGGTGGCGTGTA CATCACGGCGAAACCCCGTCTCTACTAAAAACGCAAAAAAAATTAGCCAGGCATGGTGGCGTGTA A G HM13 Ensembl:ENSG00000101294 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1213954011 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_209191,RMVar_hsa_circ_26002,RMVar_hsa_circ_209186,RMVar_hsa_circ_99051,RMVar_hsa_circ_90576,RMVar_hsa_circ_378630,RMVar_hsa_circ_209192,RMVar_hsa_circ_22046,RMVar_hsa_circ_302780,RMVar_hsa_circ_269849,RMVar_hsa_circ_209193,RMVar_hsa_circ_209194 49344 RMVar_ID_49344 Human_SNP_ID_678817482 A-to-I Human chr20 + 31550062 31550062 31550062 TTCCCTTCATACTGCTCTTTTTTTCTCCTTCTAGGTATTTGGCACCAATGTGATGGTGACAGTGG TTCCCTTCATACTGCTCTTTTTTTCTCCTTCTGGGTATTTGGCACCAATGTGATGGTGACAGTGG A G HM13 Ensembl:ENSG00000101294 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1410755742 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_62435,Human_RBP_ID_2680123,Human_RBP_ID_3960088,Human_RBP_ID_22670746,Human_RBP_ID_22766944,Human_RBP_ID_22817046,Human_RBP_ID_25627677,Human_RBP_ID_27018782,Human_RBP_ID_27295123 Human_Splice_Rec_2069979,Human_Splice_Rec_2070003,Human_Splice_Rec_2070027,Human_Splice_Rec_2070051,Human_Splice_Rec_2070075,Human_Splice_Rec_2070101,Human_Splice_Rec_2070127,Human_Splice_Rec_2070157,Human_Splice_Rec_2070175,Human_Splice_Rec_2070193,Human_Splice_Rec_2070201,Human_Splice_Rec_2070219,Human_Splice_Rec_2070235,Human_Splice_Rec_2070251,Human_Splice_Rec_2070265,Human_Splice_Rec_2070287,Human_Splice_Rec_2070293,Human_Splice_Rec_2070303,Human_Splice_Rec_2070317,Human_Splice_Rec_2070333 RMVar_hsa_circ_209191,RMVar_hsa_circ_26002,RMVar_hsa_circ_209186,RMVar_hsa_circ_99051,RMVar_hsa_circ_90576,RMVar_hsa_circ_378630,RMVar_hsa_circ_209192,RMVar_hsa_circ_108729,RMVar_hsa_circ_22046,RMVar_hsa_circ_302780,RMVar_hsa_circ_269849,RMVar_hsa_circ_209193,RMVar_hsa_circ_209194,RMVar_hsa_circ_35749,RMVar_hsa_circ_369801,RMVar_hsa_circ_209195,RMVar_hsa_circ_209196,RMVar_hsa_circ_321194 49345 RMVar_ID_49345 Human_SNP_ID_678819039 A-to-I Human chr20 + 31556106 31556106 31556106 CAGGCTGGAGTGCAATAACGCGATCTCGGCTCACTGCAACCTCTGCCTCCCTGGTTCAAGCGATT CAGGCTGGAGTGCAATAACGCGATCTCGGCTCGCTGCAACCTCTGCCTCCCTGGTTCAAGCGATT A G HM13 Ensembl:ENSG00000101294 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1034373574 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26002,RMVar_hsa_circ_90576,RMVar_hsa_circ_209192,RMVar_hsa_circ_108729,RMVar_hsa_circ_302780,RMVar_hsa_circ_209194,RMVar_hsa_circ_35749,RMVar_hsa_circ_369801,RMVar_hsa_circ_209198,RMVar_hsa_circ_209195,RMVar_hsa_circ_209196,RMVar_hsa_circ_209197,RMVar_hsa_circ_321194,RMVar_hsa_circ_272893 49346 RMVar_ID_49346 Human_SNP_ID_678819194 A-to-I Human chr20 + 31556765 31556765 31556765 GTGGCCGGCCGGGCACGGTGGCTTAAGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGTGG GTGGCCGGCCGGGCACGGTGGCTTAAGCCTGTGATCCCAGCACTTTGGGAGGCTGAGGCGGGTGG A G HM13 Ensembl:ENSG00000101294 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1364664919 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26002,RMVar_hsa_circ_90576,RMVar_hsa_circ_209192,RMVar_hsa_circ_108729,RMVar_hsa_circ_302780,RMVar_hsa_circ_209194,RMVar_hsa_circ_35749,RMVar_hsa_circ_369801,RMVar_hsa_circ_209198,RMVar_hsa_circ_209195,RMVar_hsa_circ_209196,RMVar_hsa_circ_209197,RMVar_hsa_circ_321194,RMVar_hsa_circ_272893 49347 RMVar_ID_49347 Human_SNP_ID_678819838 A-to-I Human chr20 + 31559099 31559099 31559099 TGCCACTATGTCTGGCTAATTTTTGTATTTTTAGTGAGACGAGGTTTCGCCATGTTGGCCAGGAT TGCCACTATGTCTGGCTAATTTTTGTATTTTTCGTGAGACGAGGTTTCGCCATGTTGGCCAGGAT A C HM13 Ensembl:ENSG00000101294 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6058102 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2680185,Human_RBP_ID_14058757 RMVar_hsa_circ_26002,RMVar_hsa_circ_90576,RMVar_hsa_circ_209192,RMVar_hsa_circ_108729,RMVar_hsa_circ_302780,RMVar_hsa_circ_209194,RMVar_hsa_circ_35749,RMVar_hsa_circ_369801,RMVar_hsa_circ_209198,RMVar_hsa_circ_209195,RMVar_hsa_circ_209196,RMVar_hsa_circ_209197,RMVar_hsa_circ_321194,RMVar_hsa_circ_272893 49348 RMVar_ID_49348 Human_SNP_ID_678819839 A-to-I Human chr20 + 31559099 31559099 31559099 TGCCACTATGTCTGGCTAATTTTTGTATTTTTAGTGAGACGAGGTTTCGCCATGTTGGCCAGGAT TGCCACTATGTCTGGCTAATTTTTGTATTTTTGGTGAGACGAGGTTTCGCCATGTTGGCCAGGAT A G HM13 Ensembl:ENSG00000101294 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6058102 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2680185,Human_RBP_ID_14058757 RMVar_hsa_circ_26002,RMVar_hsa_circ_90576,RMVar_hsa_circ_209192,RMVar_hsa_circ_108729,RMVar_hsa_circ_302780,RMVar_hsa_circ_209194,RMVar_hsa_circ_35749,RMVar_hsa_circ_369801,RMVar_hsa_circ_209198,RMVar_hsa_circ_209195,RMVar_hsa_circ_209196,RMVar_hsa_circ_209197,RMVar_hsa_circ_321194,RMVar_hsa_circ_272893 49349 RMVar_ID_49349 Human_SNP_ID_678820899 A-to-I Human chr20 + 31563496 31563496 31563496 CAGGCGTGCACCACCACACCCAGCTGATTTTTATATTTTTAGTAGAGACAGGGTATCACCATGTT CAGGCGTGCACCACCACACCCAGCTGATTTTTGTATTTTTAGTAGAGACAGGGTATCACCATGTT A G HM13,HM13-IT1 Ensembl:ENSG00000101294,Ensembl:ENSG00000235313 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1000713299 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25600090 RMVar_hsa_circ_39787,RMVar_hsa_circ_90576,RMVar_hsa_circ_209192,RMVar_hsa_circ_209200,RMVar_hsa_circ_123494 49350 RMVar_ID_49350 Human_SNP_ID_678820910 A-to-I Human chr20 + 31563571 31563571 31563571 GTTTCAAACTCCTGACCTCAACTGACCTGCCCACCTCAGCCTCCCAAAGTGCTGGGATTACAAGC GTTTCAAACTCCTGACCTCAACTGACCTGCCCTCCTCAGCCTCCCAAAGTGCTGGGATTACAAGC A T HM13,HM13-IT1 Ensembl:ENSG00000101294,Ensembl:ENSG00000235313 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1192068273 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39787,RMVar_hsa_circ_90576,RMVar_hsa_circ_209192,RMVar_hsa_circ_209200,RMVar_hsa_circ_123494 49351 RMVar_ID_49351 Human_SNP_ID_678820990 A-to-I Human chr20 + 31563925 31563925 31563925 ATGGAGAAACCCCATCTCTACTAAAAACACAAAATTAGCCGGGCTTGGTGGAGAATGCCTGTAAT ATGGAGAAACCCCATCTCTACTAAAAACACAACATTAGCCGGGCTTGGTGGAGAATGCCTGTAAT A C HM13,HM13-IT1 Ensembl:ENSG00000101294,Ensembl:ENSG00000235313 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs890337813 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14058935 RMVar_hsa_circ_39787,RMVar_hsa_circ_90576,RMVar_hsa_circ_209192,RMVar_hsa_circ_209200,RMVar_hsa_circ_123494 49352 RMVar_ID_49352 Human_SNP_ID_678820991 A-to-I Human chr20 + 31563925 31563925 31563925 ATGGAGAAACCCCATCTCTACTAAAAACACAAAATTAGCCGGGCTTGGTGGAGAATGCCTGTAAT ATGGAGAAACCCCATCTCTACTAAAAACACAAGATTAGCCGGGCTTGGTGGAGAATGCCTGTAAT A G HM13,HM13-IT1 Ensembl:ENSG00000101294,Ensembl:ENSG00000235313 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs890337813 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14058935 RMVar_hsa_circ_39787,RMVar_hsa_circ_90576,RMVar_hsa_circ_209192,RMVar_hsa_circ_209200,RMVar_hsa_circ_123494 49353 RMVar_ID_49353 Human_SNP_ID_678821111 A-to-I Human chr20 + 31564438 31564438 31564438 GTCTCTACAAAAAATACAAAAATTAGCCAGGCATGGAGGCGCACACCTGTAGGCCCAGCAACTTG GTCTCTACAAAAAATACAAAAATTAGCCAGGCCTGGAGGCGCACACCTGTAGGCCCAGCAACTTG A C HM13 Ensembl:ENSG00000101294 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs966840657 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14058940 RMVar_hsa_circ_39787,RMVar_hsa_circ_90576,RMVar_hsa_circ_209192,RMVar_hsa_circ_209200,RMVar_hsa_circ_123494 49354 RMVar_ID_49354 Human_SNP_ID_678821313 A-to-I Human chr20 + 31565045 31565045 31565045 AAAATTAGCCGGGCATGGTGGCAGGCACCTGTAGTCCCAGCTACTCCGGAGGCTAAGGCAGAAGA AAAATTAGCCGGGCATGGTGGCAGGCACCTGTGGTCCCAGCTACTCCGGAGGCTAAGGCAGAAGA A G HM13 Ensembl:ENSG00000101294 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1417898538 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39787,RMVar_hsa_circ_90576,RMVar_hsa_circ_209192,RMVar_hsa_circ_209200,RMVar_hsa_circ_123494 49355 RMVar_ID_49355 Human_SNP_ID_678831172 A-to-I Human chr20 + 31597769 31597769 31597769 TCCAGGAGTTCTAAACCAGCCTGGGGCAACATAGTAAGACCCCTTCTCTACAAAAAAATAAAAAA TCCAGGAGTTCTAAACCAGCCTGGGGCAACATCGTAAGACCCCTTCTCTACAAAAAAATAAAAAA A C HSALNG0129503 RNACentral:URS0000E968DE lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909239376 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2680283 49356 RMVar_ID_49356 Human_SNP_ID_678831236 A-to-I Human chr20 + 31598039 31598039 31598039 GGGTGAAAACTGAATTTCATGCCATGCGCGGTAGTTCATGCCTGTAATCCCAGCACCTTGGGAGG GGGTGAAAACTGAATTTCATGCCATGCGCGGTGGTTCATGCCTGTAATCCCAGCACCTTGGGAGG A G HSALNG0129503 RNACentral:URS0000E968DE lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971018126 Functional Loss SNV dbSNP153 33..33 33 - - - 49357 RMVar_ID_49357 Human_SNP_ID_678857014 A-to-I Human chr20 - 31690370 31690370 31690370 AAGTTTAAAATTGGCCAGGTGCAGTGACTCACACCTGTAATCCCAGCAGTTTGGGAGGCTGAGGT AAGTTTAAAATTGGCCAGGTGCAGTGACTCACTCCTGTAATCCCAGCAGTTTGGGAGGCTGAGGT T A BCL2L1 Ensembl:ENSG00000171552 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1292254451 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571446 49358 RMVar_ID_49358 Human_SNP_ID_678861501 A-to-I Human chr20 - 31709424 31709424 31709424 CCGGGAAATGGAGGTTGCAGTGAGCTGAAATCATGCCATTGCACTCCAGCTTGGGCGACAGAGGG CCGGGAAATGGAGGTTGCAGTGAGCTGAAATCGTGCCATTGCACTCCAGCTTGGGCGACAGAGGG T C BCL2L1 Ensembl:ENSG00000171552 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1394441775 Functional Loss SNV dbSNP153 33..33 33 - - - 49359 RMVar_ID_49359 Human_SNP_ID_678862775 A-to-I Human chr20 - 31715264 31715262 31715264 CTGTATTCCTTTTTTTTTTTTTTTTGAGACAGAGTCTTTCTCTGTCTCCCAGACTGGAGTGCAGT CTGTATTCCTTTTTTTTTTTTTTTTGAGACAG__TCTTTCTCTGTCTCCCAGACTGGAGTGCAGT ACT A BCL2L1 Ensembl:ENSG00000171552 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1386610678 Functional Loss DEL dbSNP153 33..34 33 - - - 49360 RMVar_ID_49360 Human_SNP_ID_678862777 A-to-I Human chr20 - 31715264 31715264 31715264 CTGTATTCCTTTTTTTTTTTTTTTTGAGACAGAGTCTTTCTCTGTCTCCCAGACTGGAGTGCAGT CTGTATTCCTTTTTTTTTTTTTTTTGAGACAGGGTCTTTCTCTGTCTCCCAGACTGGAGTGCAGT T C BCL2L1 Ensembl:ENSG00000171552 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1158485395 Functional Loss SNV dbSNP153 33..33 33 - - - 49361 RMVar_ID_49361 Human_SNP_ID_678918800 A-to-I Human chr20 + 31941113 31941113 31941113 TGCTGGCGGGCGCCTGTAGTCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCGGGA TGCTGGCGGGCGCCTGTAGTCAGCTACTCGGGGGGCTGAGGCAGGAGAATGGCGTGAACCCGGGA A G TTLL9 Ensembl:ENSG00000131044 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1163579620 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_150239 49362 RMVar_ID_49362 Human_SNP_ID_678918801 A-to-I Human chr20 + 31941119 31941119 31941119 CGGGCGCCTGTAGTCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCGGGAGGCGGA CGGGCGCCTGTAGTCAGCTACTCGGGAGGCTGCGGCAGGAGAATGGCGTGAACCCGGGAGGCGGA A C TTLL9 Ensembl:ENSG00000131044 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs553226238 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_150239 49363 RMVar_ID_49363 Human_SNP_ID_678918804 A-to-I Human chr20 + 31941126 31941126 31941126 CTGTAGTCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCGGGAGGCGGAGCTTGCA CTGTAGTCAGCTACTCGGGAGGCTGAGGCAGGTGAATGGCGTGAACCCGGGAGGCGGAGCTTGCA A T TTLL9 Ensembl:ENSG00000131044 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1164458620 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_150239 49364 RMVar_ID_49364 Human_SNP_ID_678918816 A-to-I Human chr20 + 31941177 31941170 31941178 AGGCGGAGCTTGCAGTGAGCCGAGATTGCGCCACTGCACTCCAGCCTGGGCGACAGAGCGAGACT AGGCGGAGCTTGCAGTGAGCCGAGAT________TGCACTCCAGCCTGGGCGACAGAGCGAGACT TTGCGCCAC T TTLL9 Ensembl:ENSG00000131044 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1225305227 Functional Loss DEL dbSNP153 27..34 33 - - - Human_RBP_ID_150239 49365 RMVar_ID_49365 Human_SNP_ID_678918824 A-to-I Human chr20 + 31941177 31941177 31941177 AGGCGGAGCTTGCAGTGAGCCGAGATTGCGCCACTGCACTCCAGCCTGGGCGACAGAGCGAGACT AGGCGGAGCTTGCAGTGAGCCGAGATTGCGCCCCTGCACTCCAGCCTGGGCGACAGAGCGAGACT A C TTLL9 Ensembl:ENSG00000131044 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1051085120 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_150239 49366 RMVar_ID_49366 Human_SNP_ID_678966345 A-to-I Human chr20 + 32126875 32126875 32126875 CTCCTGCCTCAGCCTCCCAGGTGGCTGGGATTACAGGCGCCTGCCACCACGCCGGCTAATTTTTG CTCCTGCCTCAGCCTCCCAGGTGGCTGGGATTCCAGGCGCCTGCCACCACGCCGGCTAATTTTTG A C TM9SF4 Ensembl:ENSG00000101337 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1197604425 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96443,RMVar_hsa_circ_209247 49367 RMVar_ID_49367 Human_SNP_ID_678966917 A-to-I Human chr20 + 32129278 32129278 32129278 ACTTTGGGAGGCTGAGGCGGGAGGATTGCTTGAGCCCAGAAGTTTGGGACCAGCCTGGGTAATAT ACTTTGGGAGGCTGAGGCGGGAGGATTGCTTGGGCCCAGAAGTTTGGGACCAGCCTGGGTAATAT A G TM9SF4 Ensembl:ENSG00000101337 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs905136586 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96443,RMVar_hsa_circ_209247 49368 RMVar_ID_49368 Human_SNP_ID_678971250 A-to-I Human chr20 + 32147591 32147591 32147591 AAACTAGGTCGGGGCTGGGCACGGTGGCTCACACCTGTTATCTCAGCACTTTGGGAGGCCAAGGC AAACTAGGTCGGGGCTGGGCACGGTGGCTCACGCCTGTTATCTCAGCACTTTGGGAGGCCAAGGC A G TM9SF4 Ensembl:ENSG00000101337 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1336402186 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107583,RMVar_hsa_circ_90758,RMVar_hsa_circ_24206,RMVar_hsa_circ_209249,RMVar_hsa_circ_209250,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_209267,RMVar_hsa_circ_102116,RMVar_hsa_circ_209266 49369 RMVar_ID_49369 Human_SNP_ID_678975564 A-to-I Human chr20 + 32164391 32164391 32164391 AATATTAGCTGGGTGTGGTGGCACACACCTATAGTCTGAGCTACTTGGGAGGCTGAGGCAGGAGG AATATTAGCTGGGTGTGGTGGCACACACCTATCGTCTGAGCTACTTGGGAGGCTGAGGCAGGAGG A C TM9SF4 Ensembl:ENSG00000101337 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1207441914 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265871,RMVar_hsa_circ_82316,RMVar_hsa_circ_209277 49370 RMVar_ID_49370 Human_SNP_ID_678983940 A-to-I Human chr20 - 32198468 32198468 32198468 GCCCATCTAATGGTTAAGATTTTGTAGAGACAAGGTCTCGCTATGTTGTTCAGGTTGGTCTGAAA GCCCATCTAATGGTTAAGATTTTGTAGAGACAGGGTCTCGCTATGTTGTTCAGGTTGGTCTGAAA T C PLAGL2 Ensembl:ENSG00000126003 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1194093126 Functional Loss SNV dbSNP153 33..33 33 - - - 49371 RMVar_ID_49371 Human_SNP_ID_678984215 A-to-I Human chr20 - 32199832 32199832 32199832 AGGCTTTCTTTTTTTTCTTTTTTTTTTGAGACAGGGTCTCACTTTTGCCCAAGCTGGAGTATAGT AGGCTTTCTTTTTTTTCTTTTTTTTTTGAGACGGGGTCTCACTTTTGCCCAAGCTGGAGTATAGT T C PLAGL2 Ensembl:ENSG00000126003 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs751134614 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6988932 49372 RMVar_ID_49372 Human_SNP_ID_678984323 A-to-I Human chr20 - 32200369 32200369 32200369 AGCTGGGCGCGGTGGCAGGCGCCTGTAGTCCCAGCTACCGGGAGGCTGAGGCAGGAGAATGGTGT AGCTGGGCGCGGTGGCAGGCGCCTGTAGTCCCGGCTACCGGGAGGCTGAGGCAGGAGAATGGTGT T C PLAGL2 Ensembl:ENSG00000126003 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs549075037 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_150208 49373 RMVar_ID_49373 Human_SNP_ID_678984416 A-to-I Human chr20 - 32200662 32200662 32200662 CACTTGAACCCAGGAGAAGGAGGTTGCAGTGAACTGAGATTGTGCCACTGTACTCCAGCCTGGGT CACTTGAACCCAGGAGAAGGAGGTTGCAGTGAGCTGAGATTGTGCCACTGTACTCCAGCCTGGGT T C PLAGL2 Ensembl:ENSG00000126003 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1443585634 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14063194,Human_RBP_ID_25600687 49374 RMVar_ID_49374 Human_SNP_ID_678984430 A-to-I Human chr20 - 32200729 32200729 32200729 AAAATTAGCTGGGTGTGGTGGCACATGCCTGTAGTCCCAGCTACTTGGGACTCTGTGGCAGGAGA AAAATTAGCTGGGTGTGGTGGCACATGCCTGTCGTCCCAGCTACTTGGGACTCTGTGGCAGGAGA T G PLAGL2 Ensembl:ENSG00000126003 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1282955917 Functional Loss SNV dbSNP153 33..33 33 - - - 49375 RMVar_ID_49375 Human_SNP_ID_678984579 A-to-I Human chr20 - 32201472 32201472 32201472 TCAAGTGATTCTCTTGACTCATTCTCCCAGGTAACTAGGATTACAGGCTTGAACCACCGCACCTG TCAAGTGATTCTCTTGACTCATTCTCCCAGGTGACTAGGATTACAGGCTTGAACCACCGCACCTG T C PLAGL2 Ensembl:ENSG00000126003 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs948127559 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14063218 49376 RMVar_ID_49376 Human_SNP_ID_678984597 A-to-I Human chr20 - 32201551 32201551 32201551 AGAAATGGGAGTCTTGCTCTGTCATCCAGGCTAGAGTACAGTGGTGCAATCAGCTCACTGCAGCC AGAAATGGGAGTCTTGCTCTGTCATCCAGGCTTGAGTACAGTGGTGCAATCAGCTCACTGCAGCC T A PLAGL2 Ensembl:ENSG00000126003 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1266221098 Functional Loss SNV dbSNP153 33..33 33 - - - 49377 RMVar_ID_49377 Human_SNP_ID_678987174 A-to-I Human chr20 + 32212333 32212333 32212333 TCTCACTGTTGCCCAGGGTGAAGTGCAGTGGCATGATCATCGCTCACTGCAGCCTCCATCTCCTC TCTCACTGTTGCCCAGGGTGAAGTGCAGTGGCTTGATCATCGCTCACTGCAGCCTCCATCTCCTC A T POFUT1 Ensembl:ENSG00000101346 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs142676756 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_344290,RMVar_hsa_circ_7724 49378 RMVar_ID_49378 Human_SNP_ID_678987282 A-to-I Human chr20 + 32212850 32212850 32212850 GTATTCTACCTGCCTTGGCCTTGCAAAGTTTTAGGATTACAGGCAAAAGCCACTGCGCCCAGCCA GTATTCTACCTGCCTTGGCCTTGCAAAGTTTTGGGATTACAGGCAAAAGCCACTGCGCCCAGCCA A G POFUT1 Ensembl:ENSG00000101346 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs918557455 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_344290,RMVar_hsa_circ_7724 49379 RMVar_ID_49379 Human_SNP_ID_678987283 A-to-I Human chr20 + 32212856 32212856 32212856 TACCTGCCTTGGCCTTGCAAAGTTTTAGGATTACAGGCAAAAGCCACTGCGCCCAGCCAGAATTT TACCTGCCTTGGCCTTGCAAAGTTTTAGGATTGCAGGCAAAAGCCACTGCGCCCAGCCAGAATTT A G POFUT1 Ensembl:ENSG00000101346 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs930045576 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_344290,RMVar_hsa_circ_7724 49380 RMVar_ID_49380 Human_SNP_ID_678989069 A-to-I Human chr20 + 32220369 32220369 32220369 CTCAGGTTGGTCTTGATCTCTTGGCCTCAAGTAATTATCCTGCCTTGGCCTCCCAAAGTGCTGGG CTCAGGTTGGTCTTGATCTCTTGGCCTCAAGTGATTATCCTGCCTTGGCCTCCCAAAGTGCTGGG A G POFUT1 Ensembl:ENSG00000101346 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs986471725 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571464 49381 RMVar_ID_49381 Human_SNP_ID_678989912 A-to-I Human chr20 + 32224182 32224182 32224182 GGGAGGCTGAGGCGGGCGGATCTTCTGAGGTCAGGAGTTTGAGACCAGCCTGGGCAACATGGCGA GGGAGGCTGAGGCGGGCGGATCTTCTGAGGTCGGGAGTTTGAGACCAGCCTGGGCAACATGGCGA A G POFUT1 Ensembl:ENSG00000101346 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs987422049 Functional Loss SNV dbSNP153 33..33 33 - - - 49382 RMVar_ID_49382 Human_SNP_ID_678990211 A-to-I Human chr20 + 32225455 32225455 32225455 GTGATCCACCTACCTTGGCTTCCCAAAGTTCTAGGATTACAGGCGTGAGCCACCGCGCCCGGTCA GTGATCCACCTACCTTGGCTTCCCAAAGTTCTGGGATTACAGGCGTGAGCCACCGCGCCCGGTCA A G POFUT1 Ensembl:ENSG00000101346 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1322407725 Functional Loss SNV dbSNP153 33..33 33 - - - 49383 RMVar_ID_49383 Human_SNP_ID_678990276 A-to-I Human chr20 + 32225664 32225664 32225664 CACACACCACAACACTTGGCTAATTTTTTGATATTTTTGGATAGATGGGGTGTTGCCATGTTGCC CACACACCACAACACTTGGCTAATTTTTTGATGTTTTTGGATAGATGGGGTGTTGCCATGTTGCC A G POFUT1 Ensembl:ENSG00000101346 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1252755220 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14063512,Human_RBP_ID_23899204 49384 RMVar_ID_49384 Human_SNP_ID_678990287 A-to-I Human chr20 + 32225764 32225764 32225764 TGCCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGAAGTGGCCACCACACCCAACCACAATTGA TGCCCACCTCAGCCTCCCAAAGTGCTGGGATTGCAGAAGTGGCCACCACACCCAACCACAATTGA A G POFUT1 Ensembl:ENSG00000101346 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1287668160 Functional Loss SNV dbSNP153 33..33 33 - - - 49385 RMVar_ID_49385 Human_SNP_ID_678991262 A-to-I Human chr20 + 32229807 32229807 32229807 ATGCTTTTTTTTTTGAGACAGAGTCTCACTCCATTGCCGAGGCTGGAGTGCAGTGGCAAGCAAAA ATGCTTTTTTTTTTGAGACAGAGTCTCACTCCGTTGCCGAGGCTGGAGTGCAGTGGCAAGCAAAA A G POFUT1 Ensembl:ENSG00000101346 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1033987500 Functional Loss SNV dbSNP153 33..33 33 - - - 49386 RMVar_ID_49386 Human_SNP_ID_678991276 A-to-I Human chr20 + 32229844 32229844 32229844 CGAGGCTGGAGTGCAGTGGCAAGCAAAATCACAGTTCACCGCATCCTCCACCTTCTGGGCTCAGG CGAGGCTGGAGTGCAGTGGCAAGCAAAATCACGGTTCACCGCATCCTCCACCTTCTGGGCTCAGG A G POFUT1 Ensembl:ENSG00000101346 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1279727908 Functional Loss SNV dbSNP153 33..33 33 - - - 49387 RMVar_ID_49387 Human_SNP_ID_679006035 A-to-I Human chr20 + 32290758 32290758 32290758 TAAATTAGCTCAGTATGGTGGCATGTACCTGTAGTCTCAGCTACTCAAAAGGCTGAGGTGGGAGG TAAATTAGCTCAGTATGGTGGCATGTACCTGTGGTCTCAGCTACTCAAAAGGCTGAGGTGGGAGG A G KIF3B Ensembl:ENSG00000101350 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1405669558 Functional Loss SNV dbSNP153 33..33 33 - - - 49388 RMVar_ID_49388 Human_SNP_ID_679006648 A-to-I Human chr20 + 32293131 32293131 32293131 AAAAAATTAGTTGGATGTGGTGGGGTGTGCTTATAGTCCCAGGTACTTGGGAGTCTGAGGTGGGA AAAAAATTAGTTGGATGTGGTGGGGTGTGCTTGTAGTCCCAGGTACTTGGGAGTCTGAGGTGGGA A G KIF3B Ensembl:ENSG00000101350 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1372297017 Functional Loss SNV dbSNP153 33..33 33 - - - 49389 RMVar_ID_49389 Human_SNP_ID_679012170 A-to-I Human chr20 + 32315498 32315498 32315498 GAGGCCAAGGCAGAGGATCTCTTGAGGCCAGGAATTCAAGACCAGCCCAGACAACATAGCAAGAT GAGGCCAAGGCAGAGGATCTCTTGAGGCCAGGCATTCAAGACCAGCCCAGACAACATAGCAAGAT A C KIF3B Ensembl:ENSG00000101350 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs575040893 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44469,RMVar_hsa_circ_319241,RMVar_hsa_circ_346622,RMVar_hsa_circ_209281 49390 RMVar_ID_49390 Human_SNP_ID_679013107 A-to-I Human chr20 + 32319229 32319229 32319229 GCAGTCTGCCCGACTTAGCCTCCCAAAGTGCTAGGATTACAAGTGTGAGCCACCATGCCCGGCCT GCAGTCTGCCCGACTTAGCCTCCCAAAGTGCTGGGATTACAAGTGTGAGCCACCATGCCCGGCCT A G KIF3B Ensembl:ENSG00000101350 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs979846399 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114097,RMVar_hsa_circ_44469,RMVar_hsa_circ_346622,RMVar_hsa_circ_209283,RMVar_hsa_circ_320632,RMVar_hsa_circ_209285,RMVar_hsa_circ_48880,RMVar_hsa_circ_209284,RMVar_hsa_circ_209289 49391 RMVar_ID_49391 Human_SNP_ID_679013108 A-to-I Human chr20 + 32319235 32319235 32319235 TGCCCGACTTAGCCTCCCAAAGTGCTAGGATTACAAGTGTGAGCCACCATGCCCGGCCTCTCCAC TGCCCGACTTAGCCTCCCAAAGTGCTAGGATTTCAAGTGTGAGCCACCATGCCCGGCCTCTCCAC A T KIF3B Ensembl:ENSG00000101350 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1367748742 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114097,RMVar_hsa_circ_44469,RMVar_hsa_circ_346622,RMVar_hsa_circ_209283,RMVar_hsa_circ_320632,RMVar_hsa_circ_209285,RMVar_hsa_circ_48880,RMVar_hsa_circ_209284,RMVar_hsa_circ_209289 49392 RMVar_ID_49392 Human_SNP_ID_679013885 A-to-I Human chr20 + 32322394 32322394 32322394 ACTTTGAGAGGCCCAGGTGGACGGATCACCTGAAGTCAGGAGTTTGAGACCAGCCCGGCCAACAT ACTTTGAGAGGCCCAGGTGGACGGATCACCTGGAGTCAGGAGTTTGAGACCAGCCCGGCCAACAT A G KIF3B Ensembl:ENSG00000101350 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1185627560 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114097,RMVar_hsa_circ_44469,RMVar_hsa_circ_346622,RMVar_hsa_circ_209283,RMVar_hsa_circ_320632,RMVar_hsa_circ_209285,RMVar_hsa_circ_48880,RMVar_hsa_circ_209284,RMVar_hsa_circ_209289 49393 RMVar_ID_49393 Human_SNP_ID_679013897 A-to-I Human chr20 + 32322461 32322461 32322461 TGAAACCCTGTCTCTACAAAAATACAGAAATTAGCCAGGCGTGGTGGCGGGTGTCTATAATCCCA TGAAACCCTGTCTCTACAAAAATACAGAAATTCGCCAGGCGTGGTGGCGGGTGTCTATAATCCCA A C KIF3B Ensembl:ENSG00000101350 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs774455993 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114097,RMVar_hsa_circ_44469,RMVar_hsa_circ_346622,RMVar_hsa_circ_209283,RMVar_hsa_circ_320632,RMVar_hsa_circ_209285,RMVar_hsa_circ_48880,RMVar_hsa_circ_209284,RMVar_hsa_circ_209289 49394 RMVar_ID_49394 Human_SNP_ID_679014884 A-to-I Human chr20 + 32323424 32323423 32323424 TTTTTTATTTTATTTATTTGTTTATTTGAGACAGAGTCTCACTTTGTCGCCAGACTGGAGTGCAG TTTTTTATTTTATTTATTTGTTTATTTGAGAC_GAGTCTCACTTTGTCGCCAGACTGGAGTGCAG CA C KIF3B Ensembl:ENSG00000101350 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1569208941 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_114097,RMVar_hsa_circ_44469,RMVar_hsa_circ_346622,RMVar_hsa_circ_209283,RMVar_hsa_circ_320632,RMVar_hsa_circ_209285,RMVar_hsa_circ_48880,RMVar_hsa_circ_209284,RMVar_hsa_circ_209289 49395 RMVar_ID_49395 Human_SNP_ID_679014974 A-to-I Human chr20 + 32323623 32323623 32323623 TTTTTCAGCCGAGCATGGTGGCTCGTACCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGTGG TTTTTCAGCCGAGCATGGTGGCTCGTACCTGTGATCCCAGCACTTTGGGAGGCTGAGGCAGGTGG A G KIF3B Ensembl:ENSG00000101350 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1242782209 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114097,RMVar_hsa_circ_44469,RMVar_hsa_circ_346622,RMVar_hsa_circ_209283,RMVar_hsa_circ_320632,RMVar_hsa_circ_209285,RMVar_hsa_circ_48880,RMVar_hsa_circ_209284,RMVar_hsa_circ_209289 49396 RMVar_ID_49396 Human_SNP_ID_679015029 A-to-I Human chr20 + 32323805 32323805 32323805 GAGGCTGAGGCAGGAAAATTGCTTGAACCTGGAAGGCGGAGGTTGCAGTGAGCCAAGATTGTGCC GAGGCTGAGGCAGGAAAATTGCTTGAACCTGGGAGGCGGAGGTTGCAGTGAGCCAAGATTGTGCC A G KIF3B Ensembl:ENSG00000101350 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1424090069 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114097,RMVar_hsa_circ_44469,RMVar_hsa_circ_346622,RMVar_hsa_circ_209283,RMVar_hsa_circ_320632,RMVar_hsa_circ_209285,RMVar_hsa_circ_48880,RMVar_hsa_circ_209284,RMVar_hsa_circ_209289 49397 RMVar_ID_49397 Human_SNP_ID_679015239 A-to-I Human chr20 + 32324771 32324771 32324771 TAAATGTAGGCAAGGTGCGGTGGCTCATGCCTATAATCCCAGCACTTTTGGAGGCTGAGGTGGGC TAAATGTAGGCAAGGTGCGGTGGCTCATGCCTGTAATCCCAGCACTTTTGGAGGCTGAGGTGGGC A G KIF3B Ensembl:ENSG00000101350 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs558617300 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114097,RMVar_hsa_circ_44469,RMVar_hsa_circ_346622,RMVar_hsa_circ_209283,RMVar_hsa_circ_320632,RMVar_hsa_circ_209285,RMVar_hsa_circ_48880,RMVar_hsa_circ_209284,RMVar_hsa_circ_209289 49398 RMVar_ID_49398 Human_SNP_ID_679015366 A-to-I Human chr20 + 32325362 32325362 32325362 AGGTGCAGGTCAACCACGCACGGCTAATTTTTATATTTTTAGTAGAGACAGGGTTTTGCCATGTT AGGTGCAGGTCAACCACGCACGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTTGCCATGTT A G KIF3B Ensembl:ENSG00000101350 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1020747477 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114097,RMVar_hsa_circ_44469,RMVar_hsa_circ_346622,RMVar_hsa_circ_209283,RMVar_hsa_circ_320632,RMVar_hsa_circ_209285,RMVar_hsa_circ_48880,RMVar_hsa_circ_209284,RMVar_hsa_circ_209289 49399 RMVar_ID_49399 Human_SNP_ID_679015367 A-to-I Human chr20 + 32325364 32325364 32325364 GTGCAGGTCAACCACGCACGGCTAATTTTTATATTTTTAGTAGAGACAGGGTTTTGCCATGTTTA GTGCAGGTCAACCACGCACGGCTAATTTTTATGTTTTTAGTAGAGACAGGGTTTTGCCATGTTTA A G KIF3B Ensembl:ENSG00000101350 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1230314045 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114097,RMVar_hsa_circ_44469,RMVar_hsa_circ_346622,RMVar_hsa_circ_209283,RMVar_hsa_circ_320632,RMVar_hsa_circ_209285,RMVar_hsa_circ_48880,RMVar_hsa_circ_209284,RMVar_hsa_circ_209289 49400 RMVar_ID_49400 Human_SNP_ID_679016278 A-to-I Human chr20 + 32329034 32329034 32329034 GGTTCAAGCAATTCTGGTGCTTCAGCCTTCCTAGTAGCTGAGACTACAGGCACATGCCACGACAC GGTTCAAGCAATTCTGGTGCTTCAGCCTTCCTGGTAGCTGAGACTACAGGCACATGCCACGACAC A G KIF3B Ensembl:ENSG00000101350 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs986712084 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114097,RMVar_hsa_circ_48880,RMVar_hsa_circ_209284,RMVar_hsa_circ_209289,RMVar_hsa_circ_209291 49401 RMVar_ID_49401 Human_SNP_ID_679017273 A-to-I Human chr20 + 32333522 32333522 32333522 TGGTGTGGTGGTGCATGCCTCTAGTCCTAGCTACTCGGGAGGCTGAGGCACGAGAATCACTTGAA TGGTGTGGTGGTGCATGCCTCTAGTCCTAGCTGCTCGGGAGGCTGAGGCACGAGAATCACTTGAA A G KIF3B Ensembl:ENSG00000101350 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1286952269 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114097,RMVar_hsa_circ_209289 49402 RMVar_ID_49402 Human_SNP_ID_679017292 A-to-I Human chr20 + 32333615 32333614 32333616 AGATAACACTACTGCATTCCAGCCTGGGTGACAGAGTGAGACTCCCCCTCAAAAAAAAAAAAAAA AGATAACACTACTGCATTCCAGCCTGGGTGAC__AGTGAGACTCCCCCTCAAAAAAAAAAAAAAA CAG C KIF3B Ensembl:ENSG00000101350 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1395239347 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_17969465 RMVar_hsa_circ_114097,RMVar_hsa_circ_209289 49403 RMVar_ID_49403 Human_SNP_ID_679019174 A-to-I Human chr20 + 32342274 32342274 32342274 CCAAGATTGTGCCACCATACTCCAGCCTGGGCAACAGAGGAGGACTCCATCCCCAAAACAAAACA CCAAGATTGTGCCACCATACTCCAGCCTGGGCGACAGAGGAGGACTCCATCCCCAAAACAAAACA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs376223959 Functional Loss SNV dbSNP153 33..33 33 - - - 49404 RMVar_ID_49404 Human_SNP_ID_679020017 A-to-I Human chr20 + 32346022 32346022 32346022 TTAGTTCAGTGCAACATCCACCTCCCTGGTTCAAGTGATCCTTCCACCTGGGCCTCCCAAGTAGC TTAGTTCAGTGCAACATCCACCTCCCTGGTTCGAGTGATCCTTCCACCTGGGCCTCCCAAGTAGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1325420704 Functional Loss SNV dbSNP153 33..33 33 - - - 49405 RMVar_ID_49405 Human_SNP_ID_679023629 A-to-I Human chr20 + 32360913 32360913 32360913 TGTTTTTCGTTTGTTTGCCACCACACCCGGCTAATTTTTTATTTTTAGTAAAGATGGGGTTTTTC TGTTTTTCGTTTGTTTGCCACCACACCCGGCTGATTTTTTATTTTTAGTAAAGATGGGGTTTTTC A G ASXL1 Ensembl:ENSG00000171456 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1287743040 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26788257 RMVar_hsa_circ_209292,RMVar_hsa_circ_123441 49406 RMVar_ID_49406 Human_SNP_ID_679023655 A-to-I Human chr20 + 32360994 32360994 32360994 GTCTCGAACTCGTGACCTTAGGTTATCCGCCCACCTTGGCCTCCCAAAGTGCTGGGATTACAGGC GTCTCGAACTCGTGACCTTAGGTTATCCGCCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGC A G ASXL1 Ensembl:ENSG00000171456 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs752959787 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_209292,RMVar_hsa_circ_123441 49407 RMVar_ID_49407 Human_SNP_ID_679023656 A-to-I Human chr20 + 32360994 32360994 32360994 GTCTCGAACTCGTGACCTTAGGTTATCCGCCCACCTTGGCCTCCCAAAGTGCTGGGATTACAGGC GTCTCGAACTCGTGACCTTAGGTTATCCGCCCTCCTTGGCCTCCCAAAGTGCTGGGATTACAGGC A T ASXL1 Ensembl:ENSG00000171456 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs752959787 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_209292,RMVar_hsa_circ_123441 49408 RMVar_ID_49408 Human_SNP_ID_679027042 A-to-I Human chr20 + 32374371 32374371 32374371 TAGATGGTGCAGTGGCACCATCATAGCTCACTACAACCTTGAGCGCCTGGGCTTAAGGAATCTTC TAGATGGTGCAGTGGCACCATCATAGCTCACTGCAACCTTGAGCGCCTGGGCTTAAGGAATCTTC A G ASXL1 Ensembl:ENSG00000171456 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs929155577 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34623,RMVar_hsa_circ_302841,RMVar_hsa_circ_127259,RMVar_hsa_circ_209303,RMVar_hsa_circ_125497,RMVar_hsa_circ_209297,RMVar_hsa_circ_209298,RMVar_hsa_circ_209295,RMVar_hsa_circ_209296,RMVar_hsa_circ_209294,RMVar_hsa_circ_80174,RMVar_hsa_circ_81512,RMVar_hsa_circ_209304,RMVar_hsa_circ_209305,RMVar_hsa_circ_107754,RMVar_hsa_circ_209307,RMVar_hsa_circ_91482,RMVar_hsa_circ_209308 49409 RMVar_ID_49409 Human_SNP_ID_679027625 A-to-I Human chr20 + 32376515 32376515 32376515 CCAGGCTGGTCTTGAACTCCTTACCTCAGGTGATCCACCCACCGCAGCCCCCCAAAGTGTTGGGA CCAGGCTGGTCTTGAACTCCTTACCTCAGGTGGTCCACCCACCGCAGCCCCCCAAAGTGTTGGGA A G ASXL1 Ensembl:ENSG00000171456 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1040895615 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34623,RMVar_hsa_circ_302841,RMVar_hsa_circ_127259,RMVar_hsa_circ_209303,RMVar_hsa_circ_125497,RMVar_hsa_circ_209297,RMVar_hsa_circ_209295,RMVar_hsa_circ_209296,RMVar_hsa_circ_209294,RMVar_hsa_circ_80174,RMVar_hsa_circ_81512,RMVar_hsa_circ_209304,RMVar_hsa_circ_209305,RMVar_hsa_circ_107754,RMVar_hsa_circ_209307,RMVar_hsa_circ_91482,RMVar_hsa_circ_209308 49410 RMVar_ID_49410 Human_SNP_ID_679027626 A-to-I Human chr20 + 32376515 32376515 32376515 CCAGGCTGGTCTTGAACTCCTTACCTCAGGTGATCCACCCACCGCAGCCCCCCAAAGTGTTGGGA CCAGGCTGGTCTTGAACTCCTTACCTCAGGTGTTCCACCCACCGCAGCCCCCCAAAGTGTTGGGA A T ASXL1 Ensembl:ENSG00000171456 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1040895615 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34623,RMVar_hsa_circ_302841,RMVar_hsa_circ_127259,RMVar_hsa_circ_209303,RMVar_hsa_circ_125497,RMVar_hsa_circ_209297,RMVar_hsa_circ_209295,RMVar_hsa_circ_209296,RMVar_hsa_circ_209294,RMVar_hsa_circ_80174,RMVar_hsa_circ_81512,RMVar_hsa_circ_209304,RMVar_hsa_circ_209305,RMVar_hsa_circ_107754,RMVar_hsa_circ_209307,RMVar_hsa_circ_91482,RMVar_hsa_circ_209308 49411 RMVar_ID_49411 Human_SNP_ID_679028435 A-to-I Human chr20 + 32378989 32378989 32378989 GTCTCTATTAAAAATAAAAAAAAAACCTAGCCAGGTGTGGTGGTGAACGCCTGTAGTCCCAGCTA GTCTCTATTAAAAATAAAAAAAAAACCTAGCCGGGTGTGGTGGTGAACGCCTGTAGTCCCAGCTA A G ASXL1 Ensembl:ENSG00000171456 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947168604 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34623,RMVar_hsa_circ_302841,RMVar_hsa_circ_127259,RMVar_hsa_circ_209303,RMVar_hsa_circ_125497,RMVar_hsa_circ_209297,RMVar_hsa_circ_209295,RMVar_hsa_circ_209296,RMVar_hsa_circ_209294,RMVar_hsa_circ_80174,RMVar_hsa_circ_81512,RMVar_hsa_circ_209304,RMVar_hsa_circ_209305,RMVar_hsa_circ_107754,RMVar_hsa_circ_209307,RMVar_hsa_circ_91482,RMVar_hsa_circ_209308 49412 RMVar_ID_49412 Human_SNP_ID_679029302 A-to-I Human chr20 + 32382035 32382035 32382035 TGGAGTGCAATGGCGCGATCTCAGCTAACGGCAACCTCCACTTCCCGGGTTCAAGTGATTCTCCT TGGAGTGCAATGGCGCGATCTCAGCTAACGGCGACCTCCACTTCCCGGGTTCAAGTGATTCTCCT A G ASXL1 Ensembl:ENSG00000171456 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1257405532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14064992 RMVar_hsa_circ_34623,RMVar_hsa_circ_302841,RMVar_hsa_circ_127259,RMVar_hsa_circ_209303,RMVar_hsa_circ_125497,RMVar_hsa_circ_209297,RMVar_hsa_circ_209295,RMVar_hsa_circ_209296,RMVar_hsa_circ_209294,RMVar_hsa_circ_80174,RMVar_hsa_circ_81512,RMVar_hsa_circ_209304,RMVar_hsa_circ_209305,RMVar_hsa_circ_107754,RMVar_hsa_circ_209307,RMVar_hsa_circ_91482,RMVar_hsa_circ_209308 49413 RMVar_ID_49413 Human_SNP_ID_679029330 A-to-I Human chr20 + 32382135 32382122 32382136 GAGGCCACCAGGCCTGGCTATTTTTATTTTTTATTTTTTATTTTTATTTTTTACTAGAGACAGTG GAGGCCACCAGGCCTGGCTA______________TTTTTATTTTTATTTTTTACTAGAGACAGTG ATTTTTATTTTTTAT A ASXL1 Ensembl:ENSG00000171456 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1054497690 Functional Loss DEL dbSNP153 21..34 33 - - - Human_RBP_ID_6989404 RMVar_hsa_circ_34623,RMVar_hsa_circ_302841,RMVar_hsa_circ_127259,RMVar_hsa_circ_209303,RMVar_hsa_circ_125497,RMVar_hsa_circ_209297,RMVar_hsa_circ_209295,RMVar_hsa_circ_209296,RMVar_hsa_circ_209294,RMVar_hsa_circ_80174,RMVar_hsa_circ_81512,RMVar_hsa_circ_209304,RMVar_hsa_circ_209305,RMVar_hsa_circ_107754,RMVar_hsa_circ_209307,RMVar_hsa_circ_91482,RMVar_hsa_circ_209308 49414 RMVar_ID_49414 Human_SNP_ID_679029331 A-to-I Human chr20 + 32382135 32382122 32382136 GAGGCCACCAGGCCTGGCTATTTTTATTTTTTATTTTTTATTTTTATTTTTTACTAGAGACAGTG GAGGCCACCAGGCCTGGCTATTTTTAT_______TTTTTATTTTTATTTTTTACTAGAGACAGTG ATTTTTATTTTTTAT ATTTTTAT ASXL1 Ensembl:ENSG00000171456 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1054497690 Functional Loss DEL dbSNP153 28..34 33 - - - Human_RBP_ID_6989404 RMVar_hsa_circ_34623,RMVar_hsa_circ_302841,RMVar_hsa_circ_127259,RMVar_hsa_circ_209303,RMVar_hsa_circ_125497,RMVar_hsa_circ_209297,RMVar_hsa_circ_209295,RMVar_hsa_circ_209296,RMVar_hsa_circ_209294,RMVar_hsa_circ_80174,RMVar_hsa_circ_81512,RMVar_hsa_circ_209304,RMVar_hsa_circ_209305,RMVar_hsa_circ_107754,RMVar_hsa_circ_209307,RMVar_hsa_circ_91482,RMVar_hsa_circ_209308 49415 RMVar_ID_49415 Human_SNP_ID_679029332 A-to-I Human chr20 + 32382135 32382135 32382135 GAGGCCACCAGGCCTGGCTATTTTTATTTTTTATTTTTTATTTTTATTTTTTACTAGAGACAGTG GAGGCCACCAGGCCTGGCTATTTTTATTTTTTTTTTTTTATTTTTATTTTTTACTAGAGACAGTG A T ASXL1 Ensembl:ENSG00000171456 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1302890445 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6989404 RMVar_hsa_circ_34623,RMVar_hsa_circ_302841,RMVar_hsa_circ_127259,RMVar_hsa_circ_209303,RMVar_hsa_circ_125497,RMVar_hsa_circ_209297,RMVar_hsa_circ_209295,RMVar_hsa_circ_209296,RMVar_hsa_circ_209294,RMVar_hsa_circ_80174,RMVar_hsa_circ_81512,RMVar_hsa_circ_209304,RMVar_hsa_circ_209305,RMVar_hsa_circ_107754,RMVar_hsa_circ_209307,RMVar_hsa_circ_91482,RMVar_hsa_circ_209308 49416 RMVar_ID_49416 Human_SNP_ID_679029423 A-to-I Human chr20 + 32382493 32382493 32382493 AACTTTGATCATCTTGTTAGAAAAAAGAGGCCAGGCACTGTGCCTCATACCTGTAATCCCAGCAT AACTTTGATCATCTTGTTAGAAAAAAGAGGCCGGGCACTGTGCCTCATACCTGTAATCCCAGCAT A G ASXL1 Ensembl:ENSG00000171456 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1004750356 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244575,Human_RBP_ID_14065014,Human_RBP_ID_17571478 RMVar_hsa_circ_34623,RMVar_hsa_circ_302841,RMVar_hsa_circ_127259,RMVar_hsa_circ_209303,RMVar_hsa_circ_125497,RMVar_hsa_circ_209297,RMVar_hsa_circ_209295,RMVar_hsa_circ_209296,RMVar_hsa_circ_209294,RMVar_hsa_circ_80174,RMVar_hsa_circ_81512,RMVar_hsa_circ_209304,RMVar_hsa_circ_209305,RMVar_hsa_circ_107754,RMVar_hsa_circ_209307,RMVar_hsa_circ_91482,RMVar_hsa_circ_209308 49417 RMVar_ID_49417 Human_SNP_ID_679030379 A-to-I Human chr20 + 32386521 32386521 32386521 CTCACTGCAACCTCCACCTCCCGAGTTTAAGTAATTCTCATGCCTTAGCCACTGGAATAGCTGGG CTCACTGCAACCTCCACCTCCCGAGTTTAAGTGATTCTCATGCCTTAGCCACTGGAATAGCTGGG A G ASXL1 Ensembl:ENSG00000171456 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs954780301 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14065220,Human_RBP_ID_17571480 RMVar_hsa_circ_34623,RMVar_hsa_circ_302841,RMVar_hsa_circ_127259,RMVar_hsa_circ_209303,RMVar_hsa_circ_125497,RMVar_hsa_circ_209297,RMVar_hsa_circ_209295,RMVar_hsa_circ_209296,RMVar_hsa_circ_209294,RMVar_hsa_circ_80174,RMVar_hsa_circ_81512,RMVar_hsa_circ_209304,RMVar_hsa_circ_209305,RMVar_hsa_circ_107754,RMVar_hsa_circ_209307,RMVar_hsa_circ_91482,RMVar_hsa_circ_209308 49418 RMVar_ID_49418 Human_SNP_ID_679030380 A-to-I Human chr20 + 32386528 32386528 32386528 CAACCTCCACCTCCCGAGTTTAAGTAATTCTCATGCCTTAGCCACTGGAATAGCTGGGATTACAG CAACCTCCACCTCCCGAGTTTAAGTAATTCTCTTGCCTTAGCCACTGGAATAGCTGGGATTACAG A T ASXL1 Ensembl:ENSG00000171456 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs987486941 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14065221,Human_RBP_ID_17571480 RMVar_hsa_circ_34623,RMVar_hsa_circ_302841,RMVar_hsa_circ_127259,RMVar_hsa_circ_209303,RMVar_hsa_circ_125497,RMVar_hsa_circ_209297,RMVar_hsa_circ_209295,RMVar_hsa_circ_209296,RMVar_hsa_circ_209294,RMVar_hsa_circ_80174,RMVar_hsa_circ_81512,RMVar_hsa_circ_209304,RMVar_hsa_circ_209305,RMVar_hsa_circ_107754,RMVar_hsa_circ_209307,RMVar_hsa_circ_91482,RMVar_hsa_circ_209308 49419 RMVar_ID_49419 Human_SNP_ID_679033559 A-to-I Human chr20 + 32399160 32399160 32399160 TTGAACCCGGGAAGCGGAGTTTGCAGTTAGCCAAGATCATGCCACTGCACTCTAGCCTGGGCGAC TTGAACCCGGGAAGCGGAGTTTGCAGTTAGCCCAGATCATGCCACTGCACTCTAGCCTGGGCGAC A C ASXL1 Ensembl:ENSG00000171456 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1262204085 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10013821,Human_RBP_ID_25629039 RMVar_hsa_circ_34623,RMVar_hsa_circ_302841,RMVar_hsa_circ_127259,RMVar_hsa_circ_209303,RMVar_hsa_circ_125497,RMVar_hsa_circ_209295,RMVar_hsa_circ_209294,RMVar_hsa_circ_80174,RMVar_hsa_circ_81512,RMVar_hsa_circ_209304,RMVar_hsa_circ_209305,RMVar_hsa_circ_107754,RMVar_hsa_circ_209307,RMVar_hsa_circ_91482,RMVar_hsa_circ_209308 49420 RMVar_ID_49420 Human_SNP_ID_679036222 A-to-I Human chr20 + 32410415 32410414 32410416 CTCCTGCACTGGTCTCCCAAAGTGTTGGGACTACAGGTGTGAGCCACTGTGCCCAGCCCCCCAAG CTCCTGCACTGGTCTCCCAAAGTGTTGGGACT__AGGTGTGAGCCACTGTGCCCAGCCCCCCAAG TAC T ASXL1 Ensembl:ENSG00000171456 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1486888927 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_34623,RMVar_hsa_circ_302841,RMVar_hsa_circ_209303,RMVar_hsa_circ_125497,RMVar_hsa_circ_209294,RMVar_hsa_circ_80174,RMVar_hsa_circ_81512,RMVar_hsa_circ_209304,RMVar_hsa_circ_209305,RMVar_hsa_circ_107754,RMVar_hsa_circ_209307,RMVar_hsa_circ_91482,RMVar_hsa_circ_209308 49421 RMVar_ID_49421 Human_SNP_ID_679036223 A-to-I Human chr20 + 32410415 32410415 32410415 CTCCTGCACTGGTCTCCCAAAGTGTTGGGACTACAGGTGTGAGCCACTGTGCCCAGCCCCCCAAG CTCCTGCACTGGTCTCCCAAAGTGTTGGGACTGCAGGTGTGAGCCACTGTGCCCAGCCCCCCAAG A G ASXL1 Ensembl:ENSG00000171456 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs555295327 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34623,RMVar_hsa_circ_302841,RMVar_hsa_circ_209303,RMVar_hsa_circ_125497,RMVar_hsa_circ_209294,RMVar_hsa_circ_80174,RMVar_hsa_circ_81512,RMVar_hsa_circ_209304,RMVar_hsa_circ_209305,RMVar_hsa_circ_107754,RMVar_hsa_circ_209307,RMVar_hsa_circ_91482,RMVar_hsa_circ_209308 49422 RMVar_ID_49422 Human_SNP_ID_679096249 A-to-I Human chr20 - 32640628 32640628 32640628 GGAGTGCAGTGGCGTGATCTCAGCTCGCTGCAACCTCCACCTTCCGGGTTCAAGTGATTCTCCTA GGAGTGCAGTGGCGTGATCTCAGCTCGCTGCAGCCTCCACCTTCCGGGTTCAAGTGATTCTCCTA T C FO393400.1,C20orf203 Ensembl:ENSG00000285382,Ensembl:ENSG00000198547 Protein coding,Protein coding 3'UTR,3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs572484534 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2071796,Human_Splice_Rec_2071797,Human_Splice_Rec_2071822,Human_Splice_Rec_2071823,Human_Splice_Rec_2071856,Human_Splice_Rec_2071857 49423 RMVar_ID_49423 Human_SNP_ID_679109037 A-to-I Human chr20 - 32692545 32692545 32692545 TTTTGTATTTTTTGTAGAGACAGATTCTCGCAATGTTGCTCAGGCTAGTCTCGAACTCCCGGCTT TTTTGTATTTTTTGTAGAGACAGATTCTCGCAGTGTTGCTCAGGCTAGTCTCGAACTCCCGGCTT T C FO393400.1 Ensembl:ENSG00000285382 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1187186771 Functional Loss SNV dbSNP153 33..33 33 - - - 49424 RMVar_ID_49424 Human_SNP_ID_679111717 A-to-I Human chr20 - 32703057 32703057 32703057 AGTTGTCACCTCCCCTTCAAAGTTCCAGAGTAAACAAATGGTGCCATCATTCAAGATAACATGCT AGTTGTCACCTCCCCTTCAAAGTTCCAGAGTAGACAAATGGTGCCATCATTCAAGATAACATGCT T C FO393400.1,COMMD7 Ensembl:ENSG00000285382,Ensembl:ENSG00000149600 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1301387944 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_561480,Human_RBP_ID_17969573,Human_RBP_ID_18444182 49425 RMVar_ID_49425 Human_SNP_ID_679122175 A-to-I Human chr20 - 32742111 32742111 32742111 GCGATCTCGGGTCACTGCAACCTCCGCCTCCCAGGTTCAACCAGTTCTCTGTCTCAGTCTCCCGA GCGATCTCGGGTCACTGCAACCTCCGCCTCCCGGGTTCAACCAGTTCTCTGTCTCAGTCTCCCGA T C FO393400.1,COMMD7 Ensembl:ENSG00000285382,Ensembl:ENSG00000149600 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs576861896 Functional Loss SNV dbSNP153 33..33 33 - - - 49426 RMVar_ID_49426 Human_SNP_ID_679151865 A-to-I Human chr20 + 32854010 32854010 32854010 TTTTGGTATTTTTTGTAGAGACGGGGTTTGCTATATTGCAGGCTGGTCTTGAACCCCTGGGCTCA TTTTGGTATTTTTTGTAGAGACGGGGTTTGCTCTATTGCAGGCTGGTCTTGAACCCCTGGGCTCA A C L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1480559546 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14068129 49427 RMVar_ID_49427 Human_SNP_ID_679151866 A-to-I Human chr20 + 32854010 32854010 32854010 TTTTGGTATTTTTTGTAGAGACGGGGTTTGCTATATTGCAGGCTGGTCTTGAACCCCTGGGCTCA TTTTGGTATTTTTTGTAGAGACGGGGTTTGCTGTATTGCAGGCTGGTCTTGAACCCCTGGGCTCA A G L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1480559546 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14068129 49428 RMVar_ID_49428 Human_SNP_ID_679152016 A-to-I Human chr20 + 32854610 32854607 32854610 TGTAATCCCAGCACTTTGGGAGGCCAGTGCAGAAGGATTGCTTGAGCCCAGGAGTTTGAAACTAG TGTAATCCCAGCACTTTGGGAGGCCAGTGC___AGGATTGCTTGAGCCCAGGAGTTTGAAACTAG CAGA C L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1271427671 Functional Loss DEL dbSNP153 31..33 33 - - - 49429 RMVar_ID_49429 Human_SNP_ID_679152025 A-to-I Human chr20 + 32854655 32854655 32854655 GCCCAGGAGTTTGAAACTAGCCTGGGCAACATAGCAAGAGACCCTGTCTCTATTTAAAAGATTTT GCCCAGGAGTTTGAAACTAGCCTGGGCAACATGGCAAGAGACCCTGTCTCTATTTAAAAGATTTT A G L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs901271717 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6990264 49430 RMVar_ID_49430 Human_SNP_ID_679278948 A-to-I Human chr20 - 33352027 33352027 33352027 TTTTGTAGGGACAGGATTTTGTCATGTTGCTCAGGCTGGTTTCCAACTCCTGGATTCAAGCGACC TTTTGTAGGGACAGGATTTTGTCATGTTGCTCTGGCTGGTTTCCAACTCCTGGATTCAAGCGACC T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1250795364 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14069912 49431 RMVar_ID_49431 Human_SNP_ID_679283545 A-to-I Human chr20 - 33371211 33371211 33371211 CAGTTCACTGCAGCCTTGACCTCCCTGGGCTCAGGTGATCCTCCCACCTCAGCCTCCTGAGTAGC CAGTTCACTGCAGCCTTGACCTCCCTGGGCTCGGGTGATCCTCCCACCTCAGCCTCCTGAGTAGC T C CDK5RAP1 Ensembl:ENSG00000101391 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs983521844 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78082,RMVar_hsa_circ_57115,RMVar_hsa_circ_96233,RMVar_hsa_circ_126054,RMVar_hsa_circ_209378,RMVar_hsa_circ_209380,RMVar_hsa_circ_209381,RMVar_hsa_circ_209385,RMVar_hsa_circ_280196,RMVar_hsa_circ_326428,RMVar_hsa_circ_338857,RMVar_hsa_circ_322708,RMVar_hsa_circ_301190,RMVar_hsa_circ_20483,RMVar_hsa_circ_333234,RMVar_hsa_circ_209383,RMVar_hsa_circ_209384,RMVar_hsa_circ_342580,RMVar_hsa_circ_209382,RMVar_hsa_circ_337486,RMVar_hsa_circ_307311,RMVar_hsa_circ_323076,RMVar_hsa_circ_209388,RMVar_hsa_circ_209390,RMVar_hsa_circ_25879,RMVar_hsa_circ_209389,RMVar_hsa_circ_209387,RMVar_hsa_circ_7262,RMVar_hsa_circ_272872,RMVar_hsa_circ_304833,RMVar_hsa_circ_314475,RMVar_hsa_circ_74454,RMVar_hsa_circ_209391 49432 RMVar_ID_49432 Human_SNP_ID_679289660 A-to-I Human chr20 - 33395405 33395405 33395405 CAGGGTCTCCCTATGTTGCCCTGGCTGGTCTCAAACTCCTGGGCTTAAGTAATCCTCCTGTCTCA CAGGGTCTCCCTATGTTGCCCTGGCTGGTCTCGAACTCCTGGGCTTAAGTAATCCTCCTGTCTCA T C CDK5RAP1 Ensembl:ENSG00000101391 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1227819672 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_301190,RMVar_hsa_circ_342580,RMVar_hsa_circ_209382,RMVar_hsa_circ_301731,RMVar_hsa_circ_27574,RMVar_hsa_circ_209393,RMVar_hsa_circ_209403,RMVar_hsa_circ_42466,RMVar_hsa_circ_319670,RMVar_hsa_circ_42662,RMVar_hsa_circ_209404,RMVar_hsa_circ_114957,RMVar_hsa_circ_299448 49433 RMVar_ID_49433 Human_SNP_ID_679293817 A-to-I Human chr20 + 33413390 33413390 33413390 ACCTCAAATGATCACCCCGCCTTCGCCCTCCAAAGTGCTGGGATTACAGGCATGAGCCACCGTGC ACCTCAAATGATCACCCCGCCTTCGCCCTCCATAGTGCTGGGATTACAGGCATGAGCCACCGTGC A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1174130992 Functional Loss SNV dbSNP153 33..33 33 - - - 49434 RMVar_ID_49434 Human_SNP_ID_679323048 A-to-I Human chr20 + 33529509 33529509 33529509 GAGACAAGCCAGGCATGGTGGCTCGCGCCTGTAATCCCAGCATTTTGGGAGGCCAAGGCTGAGGC GAGACAAGCCAGGCATGGTGGCTCGCGCCTGTGATCCCAGCATTTTGGGAGGCCAAGGCTGAGGC A G CBFA2T2 Ensembl:ENSG00000078699 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1375029697 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571503 49435 RMVar_ID_49435 Human_SNP_ID_679323329 A-to-I Human chr20 + 33530441 33530440 33530442 GTCTGATGCCCATTGTTTGTTTTTTTTGAAACAGAGTCTCACTCCGTTGCCCAGGCTGGAGTGCA GTCTGATGCCCATTGTTTGTTTTTTTTGAAAC__AGTCTCACTCCGTTGCCCAGGCTGGAGTGCA CAG C CBFA2T2 Ensembl:ENSG00000078699 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1322568282 Functional Loss DEL dbSNP153 33..34 33 - - - 49436 RMVar_ID_49436 Human_SNP_ID_679323330 A-to-I Human chr20 + 33530441 33530441 33530441 GTCTGATGCCCATTGTTTGTTTTTTTTGAAACAGAGTCTCACTCCGTTGCCCAGGCTGGAGTGCA GTCTGATGCCCATTGTTTGTTTTTTTTGAAACGGAGTCTCACTCCGTTGCCCAGGCTGGAGTGCA A G CBFA2T2 Ensembl:ENSG00000078699 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs962097481 Functional Loss SNV dbSNP153 33..33 33 - - - 49437 RMVar_ID_49437 Human_SNP_ID_679324064 A-to-I Human chr20 + 33533836 33533836 33533836 GTCTCTACTAAAAATACAGCAGTTAGCCTTGCATGGTGGTGTGTGCCTGTAATTCCAGCTACTCA GTCTCTACTAAAAATACAGCAGTTAGCCTTGCGTGGTGGTGTGTGCCTGTAATTCCAGCTACTCA A G CBFA2T2 Ensembl:ENSG00000078699 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1188253754 Functional Loss SNV dbSNP153 33..33 33 - - - 49438 RMVar_ID_49438 Human_SNP_ID_679327906 A-to-I Human chr20 + 33547561 33547561 33547561 AAAATTAACCAGGCATGGTGACATGCACCTGTAGTCCTGCTACTCAGAAGGCTGAGGTGGGAGGA AAAATTAACCAGGCATGGTGACATGCACCTGTTGTCCTGCTACTCAGAAGGCTGAGGTGGGAGGA A T CBFA2T2 Ensembl:ENSG00000078699 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1257741132 Functional Loss SNV dbSNP153 33..33 33 - - - 49439 RMVar_ID_49439 Human_SNP_ID_679343959 A-to-I Human chr20 + 33616682 33616681 33616682 CTGGGAGGCTGAGGTTGCAGTGAGCTGAGATCACACCACTGCACTCCAGCATGGGTGACAAAACA CTGGGAGGCTGAGGTTGCAGTGAGCTGAGATC_CACCACTGCACTCCAGCATGGGTGACAAAACA CA C CBFA2T2 Ensembl:ENSG00000078699 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1555845694 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_209409,RMVar_hsa_circ_12079,RMVar_hsa_circ_268254,RMVar_hsa_circ_322063,RMVar_hsa_circ_354725,RMVar_hsa_circ_377587,RMVar_hsa_circ_26567,RMVar_hsa_circ_72443,RMVar_hsa_circ_296219,RMVar_hsa_circ_345951,RMVar_hsa_circ_331545,RMVar_hsa_circ_12773,RMVar_hsa_circ_209410,RMVar_hsa_circ_209408 49440 RMVar_ID_49440 Human_SNP_ID_679348287 A-to-I Human chr20 + 33634516 33634516 33634516 CAACATGGTGAAACCCTGTCTCTACAAAAAATATGAAAATTAGCTGATTGTGGTGGTATGTGCCT CAACATGGTGAAACCCTGTCTCTACAAAAAATGTGAAAATTAGCTGATTGTGGTGGTATGTGCCT A G CBFA2T2 Ensembl:ENSG00000078699 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973168828 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268254,RMVar_hsa_circ_26567,RMVar_hsa_circ_9964,RMVar_hsa_circ_209417,RMVar_hsa_circ_289023,RMVar_hsa_circ_271326,RMVar_hsa_circ_209416,RMVar_hsa_circ_61315,RMVar_hsa_circ_356502,RMVar_hsa_circ_278234,RMVar_hsa_circ_341943,RMVar_hsa_circ_209424,RMVar_hsa_circ_209423,RMVar_hsa_circ_359658 49441 RMVar_ID_49441 Human_SNP_ID_679348288 A-to-I Human chr20 + 33634516 33634516 33634516 CAACATGGTGAAACCCTGTCTCTACAAAAAATATGAAAATTAGCTGATTGTGGTGGTATGTGCCT CAACATGGTGAAACCCTGTCTCTACAAAAAATTTGAAAATTAGCTGATTGTGGTGGTATGTGCCT A T CBFA2T2 Ensembl:ENSG00000078699 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973168828 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268254,RMVar_hsa_circ_26567,RMVar_hsa_circ_9964,RMVar_hsa_circ_209417,RMVar_hsa_circ_289023,RMVar_hsa_circ_271326,RMVar_hsa_circ_209416,RMVar_hsa_circ_61315,RMVar_hsa_circ_356502,RMVar_hsa_circ_278234,RMVar_hsa_circ_341943,RMVar_hsa_circ_209424,RMVar_hsa_circ_209423,RMVar_hsa_circ_359658 49442 RMVar_ID_49442 Human_SNP_ID_679349446 A-to-I Human chr20 + 33639423 33639423 33639423 GGTGAAACCCTGTCTCTATTAAAAATACAAAAAATTAGCCAGGTGTGGTGGCGGGCACCTGTAGT GGTGAAACCCTGTCTCTATTAAAAATACAAAACATTAGCCAGGTGTGGTGGCGGGCACCTGTAGT A C CBFA2T2 Ensembl:ENSG00000078699 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs868811023 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268254,RMVar_hsa_circ_26567,RMVar_hsa_circ_9964,RMVar_hsa_circ_209417,RMVar_hsa_circ_289023,RMVar_hsa_circ_61315,RMVar_hsa_circ_341943,RMVar_hsa_circ_209423,RMVar_hsa_circ_209426,RMVar_hsa_circ_304838 49443 RMVar_ID_49443 Human_SNP_ID_679349460 A-to-I Human chr20 + 33639467 33639467 33639467 GTGGTGGCGGGCACCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATGGCGTGAACCCG GTGGTGGCGGGCACCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCG A G CBFA2T2 Ensembl:ENSG00000078699 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1386316717 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268254,RMVar_hsa_circ_26567,RMVar_hsa_circ_9964,RMVar_hsa_circ_209417,RMVar_hsa_circ_289023,RMVar_hsa_circ_61315,RMVar_hsa_circ_341943,RMVar_hsa_circ_209423,RMVar_hsa_circ_209426,RMVar_hsa_circ_304838 49444 RMVar_ID_49444 Human_SNP_ID_679349735 A-to-I Human chr20 + 33640432 33640432 33640432 GAGGCAGAGCAGAAAGCCTTTGAAGTGATTGCAACAGAGAGAGCACGAATGGAGCAAACCATAGC GAGGCAGAGCAGAAAGCCTTTGAAGTGATTGCGACAGAGAGAGCACGAATGGAGCAAACCATAGC A G CBFA2T2 Ensembl:ENSG00000078699 Protein coding CDS GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1248473770 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_61960,Human_RBP_ID_8235083 Human_Splice_Rec_2073014,Human_Splice_Rec_2073015,Human_Splice_Rec_2073036,Human_Splice_Rec_2073037,Human_Splice_Rec_2073068,Human_Splice_Rec_2073069,Human_Splice_Rec_2073088,Human_Splice_Rec_2073089,Human_Splice_Rec_2073112,Human_Splice_Rec_2073113,Human_Splice_Rec_2073132,Human_Splice_Rec_2073133,Human_Splice_Rec_2073148,Human_Splice_Rec_2073149 RMVar_hsa_circ_268254,RMVar_hsa_circ_26567,RMVar_hsa_circ_9964,RMVar_hsa_circ_209417,RMVar_hsa_circ_289023,RMVar_hsa_circ_61315,RMVar_hsa_circ_341943,RMVar_hsa_circ_209423,RMVar_hsa_circ_209426,RMVar_hsa_circ_304838,RMVar_hsa_circ_347689 49445 RMVar_ID_49445 Human_SNP_ID_679351375 A-to-I Human chr20 + 33646027 33646027 33646027 TGTTTTTTGTTGTTGTGGTGGTTTTTTAACACAAAGTCTCACTCTGTTGCCCAGGCTGGAGTGCA TGTTTTTTGTTGTTGTGGTGGTTTTTTAACACGAAGTCTCACTCTGTTGCCCAGGCTGGAGTGCA A G CBFA2T2 Ensembl:ENSG00000078699 Protein coding 3'UTR GSE47997;GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,24183664,31158229,31158229 RNA-Seq:(High) rs948101274 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268254 49446 RMVar_ID_49446 Human_SNP_ID_679351376 A-to-I Human chr20 + 33646028 33646028 33646028 GTTTTTTGTTGTTGTGGTGGTTTTTTAACACAAAGTCTCACTCTGTTGCCCAGGCTGGAGTGCAG GTTTTTTGTTGTTGTGGTGGTTTTTTAACACAGAGTCTCACTCTGTTGCCCAGGCTGGAGTGCAG A G CBFA2T2 Ensembl:ENSG00000078699 Protein coding 3'UTR GSE47997;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,31158229,31158229 RNA-Seq:(High) rs779697630 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268254 49447 RMVar_ID_49447 Human_SNP_ID_679351446 A-to-I Human chr20 + 33646261 33646261 33646261 CCTGACCTCAGGTGACCTGCCTTGGCCTCCCAAAGTGCAGGGATTACAAGCGTGAGCCACCATGC CCTGACCTCAGGTGACCTGCCTTGGCCTCCCAGAGTGCAGGGATTACAAGCGTGAGCCACCATGC A G CBFA2T2 Ensembl:ENSG00000078699 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490829,GSM3490830,GSM3490831 Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,EC109 cell line - 31158229,32596459 RNA-Seq:(High) rs1211153112 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268254 49448 RMVar_ID_49448 Human_SNP_ID_679351569 A-to-I Human chr20 + 33646730 33646730 33646730 AAAAAATAGAAAAATCAGCCGGGTGTGGTGGCACACACCTGTAATCCTAGCTACTCAGGAGGCTG AAAAAATAGAAAAATCAGCCGGGTGTGGTGGCGCACACCTGTAATCCTAGCTACTCAGGAGGCTG A G CBFA2T2 Ensembl:ENSG00000078699 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs765350944 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268254 49449 RMVar_ID_49449 Human_SNP_ID_679351573 A-to-I Human chr20 + 33646767 33646767 33646767 CCTGTAATCCTAGCTACTCAGGAGGCTGAGGCAAGAGAATCTCTTGAACCTGTGAGCCAGAGGTT CCTGTAATCCTAGCTACTCAGGAGGCTGAGGCGAGAGAATCTCTTGAACCTGTGAGCCAGAGGTT A G CBFA2T2 Ensembl:ENSG00000078699 Protein coding 3'UTR GSE47997;GSE126723:GSM3611827,GSM3611828,GSM3611829 K562 cells&HepG2 cells;Bronchiolar epithelium,BEP2D cell line - 23474544,31158229 RNA-Seq:(High) rs1476070462 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268254 49450 RMVar_ID_49450 Human_SNP_ID_679351937 A-to-I Human chr20 + 33648140 33648140 33648140 GGAAATTCAGCCTGCTTAGAGGACTGACCTCTACAGTTCATATTTGCAGTGACATAAAAGGCAAA GGAAATTCAGCCTGCTTAGAGGACTGACCTCTGCAGTTCATATTTGCAGTGACATAAAAGGCAAA A G CBFA2T2 Ensembl:ENSG00000078699 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1269800647 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_268254 49451 RMVar_ID_49451 Human_SNP_ID_679352594 A-to-I Human chr20 - 33650641 33650641 33650641 TAATTTGGCCGGGTGCAGTGGCTCATGCTTGTAGTCCCAGGACTTTGGCGGGGGCGAGGCAGGCA TAATTTGGCCGGGTGCAGTGGCTCATGCTTGTTGTCCCAGGACTTTGGCGGGGGCGAGGCAGGCA T A lnc-NECAB3-1 RNACentral:URS00008B2609 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1312672423 Functional Loss SNV dbSNP153 33..33 33 - - - 49452 RMVar_ID_49452 Human_SNP_ID_679354073 A-to-I Human chr20 - 33655980 33655980 33655980 GGCTTGTTCGGGTGTAGTTGTGTGTGCCTGTAATTCCAGCTACTTGGGAGGCTGAGGCAGGAGAA GGCTTGTTCGGGTGTAGTTGTGTGTGCCTGTAGTTCCAGCTACTTGGGAGGCTGAGGCAGGAGAA T C AL121906.2 Ensembl:ENSG00000275223 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs969391096 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26788303 49453 RMVar_ID_49453 Human_SNP_ID_679356223 A-to-I Human chr20 - 33662789 33662789 33662789 GGACTGCGGGCATTCACCACCACAACCAGCTAAGTTTTAATTTTTGTAGAGATGGGGCCTCCCTA GGACTGCGGGCATTCACCACCACAACCAGCTAGGTTTTAATTTTTGTAGAGATGGGGCCTCCCTA T C NECAB3 Ensembl:ENSG00000125967 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs926919618 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87979,RMVar_hsa_circ_110565,RMVar_hsa_circ_209430,RMVar_hsa_circ_209431,RMVar_hsa_circ_104944,RMVar_hsa_circ_209432 49454 RMVar_ID_49454 Human_SNP_ID_679368416 A-to-I Human chr20 - 33705050 33705050 33705050 GGGGGGCTGCTGTGAGCCGAGATAGTTCCATTACACTTCAGCCTGGGTGACAGAGTAAGACTCTG GGGGGGCTGCTGTGAGCCGAGATAGTTCCATTTCACTTCAGCCTGGGTGACAGAGTAAGACTCTG T A PXMP4 Ensembl:ENSG00000101417 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167467467 Functional Loss SNV dbSNP153 33..33 33 - - - 49455 RMVar_ID_49455 Human_SNP_ID_679368655 A-to-I Human chr20 - 33705998 33705998 33705998 TCGCTTGAACCTGGGAGGCAGAGGCTGCAGTGAGCTGAGATCGCACGACTGCACTCCAGCCTGGG TCGCTTGAACCTGGGAGGCAGAGGCTGCAGTGGGCTGAGATCGCACGACTGCACTCCAGCCTGGG T C PXMP4 Ensembl:ENSG00000101417 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1293696248 Functional Loss SNV dbSNP153 33..33 33 - - - 49456 RMVar_ID_49456 Human_SNP_ID_679368726 A-to-I Human chr20 - 33706370 33706370 33706370 TAGGGCTAGTCTCGACCTCCTAGCCTCAAGCAATCTTCCTGCCTCAGTCTCCCAAAGTGCCATGA TAGGGCTAGTCTCGACCTCCTAGCCTCAAGCAGTCTTCCTGCCTCAGTCTCCCAAAGTGCCATGA T C PXMP4 Ensembl:ENSG00000101417 Protein coding 3'UTR GSE123020:GSM3490829,GSM3490830,GSM3490831 esophageal squamous carcinoma cells,EC109 cell line - 32596459 RNA-Seq:(High) rs528171080 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26489609 49457 RMVar_ID_49457 Human_SNP_ID_679368734 A-to-I Human chr20 - 33706395 33706395 33706395 TAGCGACAGGGTCTCGCTCTGTCACTAGGGCTAGTCTCGACCTCCTAGCCTCAAGCAATCTTCCT TAGCGACAGGGTCTCGCTCTGTCACTAGGGCTTGTCTCGACCTCCTAGCCTCAAGCAATCTTCCT T A PXMP4 Ensembl:ENSG00000101417 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1347963297 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17969893 49458 RMVar_ID_49458 Human_SNP_ID_679369410 A-to-I Human chr20 - 33709169 33709168 33709170 CTATCTCAGCCTCCCAAGTAGCTGGGACTACAAGCGCCTGCCACCATACCAGCTAATTTTTGTAT CTATCTCAGCCTCCCAAGTAGCTGGGACTAC__GCGCCTGCCACCATACCAGCTAATTTTTGTAT CTT C PXMP4 Ensembl:ENSG00000101417 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1188339395 Functional Loss DEL dbSNP153 32..33 33 - - - 49459 RMVar_ID_49459 Human_SNP_ID_679381272 A-to-I Human chr20 + 33756164 33756164 33756164 AGGGTTGCTTGAGCCTGGGAGGTCAAGGCTGCAGTGAGCCGAGATCACATCATTGCATTCCAGCC AGGGTTGCTTGAGCCTGGGAGGTCAAGGCTGCCGTGAGCCGAGATCACATCATTGCATTCCAGCC A C ZNF341 Ensembl:ENSG00000131061 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1451113483 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47314,RMVar_hsa_circ_377337,RMVar_hsa_circ_51971,RMVar_hsa_circ_72233,RMVar_hsa_circ_65326 49460 RMVar_ID_49460 Human_SNP_ID_679385155 A-to-I Human chr20 + 33771420 33771420 33771420 AGGCATGTGCCCCACGCCCAGCTAATTTTTGTATTTTTTGTAGAGACGGGGTTTCGCCATGTTGC AGGCATGTGCCCCACGCCCAGCTAATTTTTGTCTTTTTTGTAGAGACGGGGTTTCGCCATGTTGC A C ZNF341 Ensembl:ENSG00000131061 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1390294985 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47314,RMVar_hsa_circ_209446,RMVar_hsa_circ_79140,RMVar_hsa_circ_72233,RMVar_hsa_circ_27160,RMVar_hsa_circ_269026,RMVar_hsa_circ_103478,RMVar_hsa_circ_209443,RMVar_hsa_circ_209444,RMVar_hsa_circ_359736,RMVar_hsa_circ_46476 49461 RMVar_ID_49461 Human_SNP_ID_679388932 A-to-I Human chr20 + 33788312 33788312 33788312 GTGGTGGCACACACCTGTAATCCCATCTACTCAGGAGGCTGAGGTAGGAGGATTGCTTGAACCCA GTGGTGGCACACACCTGTAATCCCATCTACTCCGGAGGCTGAGGTAGGAGGATTGCTTGAACCCA A C ZNF341 Ensembl:ENSG00000131061 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs918872600 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79140,RMVar_hsa_circ_209444,RMVar_hsa_circ_209449,RMVar_hsa_circ_90944,RMVar_hsa_circ_311758,RMVar_hsa_circ_295588,RMVar_hsa_circ_209450,RMVar_hsa_circ_209448 49462 RMVar_ID_49462 Human_SNP_ID_679388933 A-to-I Human chr20 + 33788312 33788312 33788312 GTGGTGGCACACACCTGTAATCCCATCTACTCAGGAGGCTGAGGTAGGAGGATTGCTTGAACCCA GTGGTGGCACACACCTGTAATCCCATCTACTCGGGAGGCTGAGGTAGGAGGATTGCTTGAACCCA A G ZNF341 Ensembl:ENSG00000131061 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs918872600 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79140,RMVar_hsa_circ_209444,RMVar_hsa_circ_209449,RMVar_hsa_circ_90944,RMVar_hsa_circ_311758,RMVar_hsa_circ_295588,RMVar_hsa_circ_209450,RMVar_hsa_circ_209448 49463 RMVar_ID_49463 Human_SNP_ID_679402630 A-to-I Human chr20 + 33849341 33849341 33849341 TGCATTTGGGCTGGGTGAGGTGGCTCACGCCTATAATTCCAGCACTTTGGGAGGCTGAGGCAGGC TGCATTTGGGCTGGGTGAGGTGGCTCACGCCTGTAATTCCAGCACTTTGGGAGGCTGAGGCAGGC A G CHMP4B Ensembl:ENSG00000101421 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1399988149 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16427,RMVar_hsa_circ_93031,RMVar_hsa_circ_118507,RMVar_hsa_circ_209452,RMVar_hsa_circ_209453 49464 RMVar_ID_49464 Human_SNP_ID_679402672 A-to-I Human chr20 + 33849547 33849547 33849547 TTGAACCCAGGAAGTGGAAGTTGCAGTGAGCCAAAATTGCACCACTGCACTCCAGCCTGGGCGAC TTGAACCCAGGAAGTGGAAGTTGCAGTGAGCCTAAATTGCACCACTGCACTCCAGCCTGGGCGAC A T CHMP4B Ensembl:ENSG00000101421 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1043175997 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16427,RMVar_hsa_circ_93031,RMVar_hsa_circ_118507,RMVar_hsa_circ_209452,RMVar_hsa_circ_209453 49465 RMVar_ID_49465 Human_SNP_ID_679402767 A-to-I Human chr20 + 33849997 33849997 33849997 TGGGGTCTCACTGTGTTGCCCAGACTGGTCTCAAACTCCTGGCCTCAAGTGATCCTCCCTCCTGG TGGGGTCTCACTGTGTTGCCCAGACTGGTCTCGAACTCCTGGCCTCAAGTGATCCTCCCTCCTGG A G CHMP4B Ensembl:ENSG00000101421 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs191505850 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16427,RMVar_hsa_circ_93031,RMVar_hsa_circ_118507,RMVar_hsa_circ_209452,RMVar_hsa_circ_209453 49466 RMVar_ID_49466 Human_SNP_ID_679437304 A-to-I Human chr20 - 33990884 33990884 33990884 AGAGGATCACTTGAGCCCAGGAGGCCAAGGCTACAGTGAGACATGCTCACACCACTGCATCCAGC AGAGGATCACTTGAGCCCAGGAGGCCAAGGCTTCAGTGAGACATGCTCACACCACTGCATCCAGC T A RALY-AS1 Ensembl:ENSG00000285230 lincRNA intron GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line - 24183664,31158229 RNA-Seq:(High) rs867043252 Functional Loss SNV dbSNP153 33..33 33 - - - 49467 RMVar_ID_49467 Human_SNP_ID_679437305 A-to-I Human chr20 - 33990884 33990884 33990884 AGAGGATCACTTGAGCCCAGGAGGCCAAGGCTACAGTGAGACATGCTCACACCACTGCATCCAGC AGAGGATCACTTGAGCCCAGGAGGCCAAGGCTCCAGTGAGACATGCTCACACCACTGCATCCAGC T G RALY-AS1 Ensembl:ENSG00000285230 lincRNA intron GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line - 24183664,31158229 RNA-Seq:(High) rs867043252 Functional Loss SNV dbSNP153 33..33 33 - - - 49468 RMVar_ID_49468 Human_SNP_ID_679461468 A-to-I Human chr20 + 34086057 34086055 34086057 TCAGGGTCTCACCCAGGTTGGAATGCAGTGGCACAATCTCTCGGCTCACTGCAACCTCTGTCTCC TCAGGGTCTCACCCAGGTTGGAATGCAGTGG__CAATCTCTCGGCTCACTGCAACCTCTGTCTCC GCA G RALY Ensembl:ENSG00000125970 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1265143634 Functional Loss DEL dbSNP153 32..33 33 - - - 49469 RMVar_ID_49469 Human_SNP_ID_679464878 A-to-I Human chr20 - 34099300 34099300 34099300 CAGGCTGGAGTGCGGTGGCACGATCTCAACTCACTGCAACCTCTGCTTCCTGGGTTCAAGCGATT CAGGCTGGAGTGCGGTGGCACGATCTCAACTCCCTGCAACCTCTGCTTCCTGGGTTCAAGCGATT T G EIF2S2 Ensembl:ENSG00000125977 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947212214 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19288,RMVar_hsa_circ_59414,RMVar_hsa_circ_327464,RMVar_hsa_circ_308503,RMVar_hsa_circ_363726,RMVar_hsa_circ_347622 49470 RMVar_ID_49470 Human_SNP_ID_679499744 A-to-I Human chr20 - 34245544 34245544 34245544 TCTACCAAAAAAAATACAAAATTTAGCCAGGCATGGTGGCGCACACCTGTAGTCCCAGCTACTCA TCTACCAAAAAAAATACAAAATTTAGCCAGGCGTGGTGGCGCACACCTGTAGTCCCAGCTACTCA T C AL035458.2 Ensembl:ENSG00000250917 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1036979753 Functional Loss SNV dbSNP153 33..33 33 - - - 49471 RMVar_ID_49471 Human_SNP_ID_679502461 A-to-I Human chr20 - 34257224 34257224 34257224 TAACCAGGTGGTGGCCTCCTGAGTAGATGCCTATAAATCCACCTACTCAGGAGGCTGAGGCAGGA TAACCAGGTGGTGGCCTCCTGAGTAGATGCCTGTAAATCCACCTACTCAGGAGGCTGAGGCAGGA T C AL035458.2 Ensembl:ENSG00000250917 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1457363195 Functional Loss SNV dbSNP153 33..33 33 - - - 49472 RMVar_ID_49472 Human_SNP_ID_679502489 A-to-I Human chr20 - 34257360 34257352 34257361 ATTCAACCCGGCTGGGCTGGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCTGAAGCGAAT ATTCAACCCGGCTGGGCTGGTGGCTCACGCC_________AGCACTTTGGGAGGCTGAAGCGAAT TGGGATTATA T AL035458.2 Ensembl:ENSG00000250917 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1568767991 Functional Loss DEL dbSNP153 32..40 33 - - - 49473 RMVar_ID_49473 Human_SNP_ID_679503214 A-to-I Human chr20 - 34259598 34259598 34259598 AGGGCTACAGGTGCCCATCACTATGCCAGGCTAATTTTTGTATTTTTTGTAGAGACAGGATTTTA AGGGCTACAGGTGCCCATCACTATGCCAGGCTGATTTTTGTATTTTTTGTAGAGACAGGATTTTA T C AL035458.2 Ensembl:ENSG00000250917 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928037895 Functional Loss SNV dbSNP153 33..33 33 - - - 49474 RMVar_ID_49474 Human_SNP_ID_679505278 A-to-I Human chr20 - 34268506 34268506 34268506 ATTGTCCAGGTTGGTCTCAAACTCTTGAGCTAAAGTGATCTGCCTGCCTCGGCCTCCCAAAGTGC ATTGTCCAGGTTGGTCTCAAACTCTTGAGCTAGAGTGATCTGCCTGCCTCGGCCTCCCAAAGTGC T C AL035458.2 Ensembl:ENSG00000250917 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1471617756 Functional Loss SNV dbSNP153 33..33 33 - - - 49475 RMVar_ID_49475 Human_SNP_ID_679506917 A-to-I Human chr20 - 34274725 34274725 34274725 CCAGGCTGGTCTCAAACTCCTGGGCTCAAGCAATCCTCCTGCCTCGGCCTCCCAAAGTGCTGGAA CCAGGCTGGTCTCAAACTCCTGGGCTCAAGCAGTCCTCCTGCCTCGGCCTCCCAAAGTGCTGGAA T C AL035458.2 Ensembl:ENSG00000250917 lincRNA intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs761924730 Functional Loss SNV dbSNP153 33..33 33 - - - 49476 RMVar_ID_49476 Human_SNP_ID_679506954 A-to-I Human chr20 - 34274844 34274844 34274844 GCTCAAGCGATCCTCCTGCCTCAGCCTCCCAAATAGCTCAGACTACAGGCGCGTGCCACCACACC GCTCAAGCGATCCTCCTGCCTCAGCCTCCCAAGTAGCTCAGACTACAGGCGCGTGCCACCACACC T C AL035458.2 Ensembl:ENSG00000250917 lincRNA intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs980976888 Functional Loss SNV dbSNP153 33..33 33 - - - 49477 RMVar_ID_49477 Human_SNP_ID_679506955 A-to-I Human chr20 - 34274845 34274845 34274845 AGCTCAAGCGATCCTCCTGCCTCAGCCTCCCAAATAGCTCAGACTACAGGCGCGTGCCACCACAC AGCTCAAGCGATCCTCCTGCCTCAGCCTCCCAGATAGCTCAGACTACAGGCGCGTGCCACCACAC T C AL035458.2 Ensembl:ENSG00000250917 lincRNA intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1457202972 Functional Loss SNV dbSNP153 33..33 33 - - - 49478 RMVar_ID_49478 Human_SNP_ID_679506998 A-to-I Human chr20 - 34275050 34275050 34275050 GACTGGATTCGCCCCCAAGACTGCCTTGTCCAATCCCTTCATGGTGCAGCTGGGAGGGAATTTTG GACTGGATTCGCCCCCAAGACTGCCTTGTCCAGTCCCTTCATGGTGCAGCTGGGAGGGAATTTTG T C AL035458.2 Ensembl:ENSG00000250917 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348640979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8260587,Human_RBP_ID_17571510 49479 RMVar_ID_49479 Human_SNP_ID_679506999 A-to-I Human chr20 - 34275050 34275050 34275050 GACTGGATTCGCCCCCAAGACTGCCTTGTCCAATCCCTTCATGGTGCAGCTGGGAGGGAATTTTG GACTGGATTCGCCCCCAAGACTGCCTTGTCCACTCCCTTCATGGTGCAGCTGGGAGGGAATTTTG T G AL035458.2 Ensembl:ENSG00000250917 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348640979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8260587,Human_RBP_ID_17571510 49480 RMVar_ID_49480 Human_SNP_ID_679507223 A-to-I Human chr20 - 34275814 34275814 34275814 AAATTAGCCGGGCATGGTGATGCACGCCTGTAATCCCAGCTACTCAGGAGGCTGAGACAGGAAAA AAATTAGCCGGGCATGGTGATGCACGCCTGTATTCCCAGCTACTCAGGAGGCTGAGACAGGAAAA T A AL035458.2 Ensembl:ENSG00000250917 lincRNA intron GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs904958553 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5249696 49481 RMVar_ID_49481 Human_SNP_ID_679507272 A-to-I Human chr20 - 34275970 34275970 34275970 GAAGCCAACACAGACCGGGTGCAGCAGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGT GAAGCCAACACAGACCGGGTGCAGCAGCTCACTCCTGTAATCCCAGCACTTTGGGAGGCCAAGGT T A AL035458.2 Ensembl:ENSG00000250917 lincRNA intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs983416720 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3657403 49482 RMVar_ID_49482 Human_SNP_ID_679507588 A-to-I Human chr20 - 34277505 34277505 34277505 CTTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGTGCCCGGCCTTTATGCTGAGTT CTTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGTGCCCGGCCTTTATGCTGAGTT T C AL035458.2 Ensembl:ENSG00000250917 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs999334950 Functional Loss SNV dbSNP153 33..33 33 - - - 49483 RMVar_ID_49483 Human_SNP_ID_679510512 A-to-I Human chr20 - 34289378 34289378 34289378 ACGAGGTCAGGAGTTTGAGACCAGTCTGGCCAACATAGTGAAACCCCGTCTCTACTAAAAATACA ACGAGGTCAGGAGTTTGAGACCAGTCTGGCCAGCATAGTGAAACCCCGTCTCTACTAAAAATACA T C AHCY Ensembl:ENSG00000101444 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1205354 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_209484,RMVar_hsa_circ_78733,RMVar_hsa_circ_125171,RMVar_hsa_circ_342507,RMVar_hsa_circ_370859,RMVar_hsa_circ_93593,RMVar_hsa_circ_209486,RMVar_hsa_circ_209487,RMVar_hsa_circ_209488,RMVar_hsa_circ_209485 49484 RMVar_ID_49484 Human_SNP_ID_679531264 A-to-I Human chr20 + 34371325 34371325 34371325 TTTTTTTTTTGAGATGGAGCCTTCCCCAGGCTAGAGTGCAATGGCACGATCTTGGCTCACTGCAG TTTTTTTTTTGAGATGGAGCCTTCCCCAGGCTGGAGTGCAATGGCACGATCTTGGCTCACTGCAG A G ITCH Ensembl:ENSG00000078747 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1347479415 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571512 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 49485 RMVar_ID_49485 Human_SNP_ID_679531789 A-to-I Human chr20 + 34373148 34373148 34373148 AGGCATGTGCCACCACGCCCAGCTAATTTTGTATTTTTACTAGAGATAGGGTTTCACTGTGTTGG AGGCATGTGCCACCACGCCCAGCTAATTTTGTGTTTTTACTAGAGATAGGGTTTCACTGTGTTGG A G ITCH Ensembl:ENSG00000078747 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1275783679 Functional Loss SNV dbSNP153 33..33 33 - - - 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 49486 RMVar_ID_49486 Human_SNP_ID_679533212 A-to-I Human chr20 + 34378351 34378351 34378351 AAAAATTAGCCGGGTGGGGTGGTGGCGCACCTATAATCCCAGATACTCGGTGGGCTGAGGCTGGA AAAAATTAGCCGGGTGGGGTGGTGGCGCACCTGTAATCCCAGATACTCGGTGGGCTGAGGCTGGA A G ITCH Ensembl:ENSG00000078747 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1214840721 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14075898,Human_RBP_ID_25603211 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 49487 RMVar_ID_49487 Human_SNP_ID_679535933 A-to-I Human chr20 + 34387779 34387779 34387779 CAGACTGGAGTGTAGTGGTATGATCTTAGCTCACTGTAACCTCCGCCTCCTGGGTTCAAGCGGTT CAGACTGGAGTGTAGTGGTATGATCTTAGCTCGCTGTAACCTCCGCCTCCTGGGTTCAAGCGGTT A G ITCH Ensembl:ENSG00000078747 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1042744698 Functional Loss SNV dbSNP153 33..33 33 - - - 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 49488 RMVar_ID_49488 Human_SNP_ID_679544520 A-to-I Human chr20 + 34421272 34421272 34421272 GAGTAGCTGGGACTTCAGGTGCTCACCACCATACCTGGCTTCAGTTCACTTTTTTGTTTTTGAGA GAGTAGCTGGGACTTCAGGTGCTCACCACCATGCCTGGCTTCAGTTCACTTTTTTGTTTTTGAGA A G ITCH Ensembl:ENSG00000078747 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1226902872 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35941,RMVar_hsa_circ_25995,RMVar_hsa_circ_70065,RMVar_hsa_circ_348572,RMVar_hsa_circ_353174,RMVar_hsa_circ_42653,RMVar_hsa_circ_68688,RMVar_hsa_circ_209509,RMVar_hsa_circ_306658,RMVar_hsa_circ_73725,RMVar_hsa_circ_54559,RMVar_hsa_circ_2423,RMVar_hsa_circ_20385,RMVar_hsa_circ_15901,RMVar_hsa_circ_74558,RMVar_hsa_circ_359910,RMVar_hsa_circ_303559,RMVar_hsa_circ_17294,RMVar_hsa_circ_345132,RMVar_hsa_circ_360443,RMVar_hsa_circ_362008,RMVar_hsa_circ_352182,RMVar_hsa_circ_332425,RMVar_hsa_circ_342814,RMVar_hsa_circ_331034,RMVar_hsa_circ_298207,RMVar_hsa_circ_312079,RMVar_hsa_circ_317530,RMVar_hsa_circ_303750,RMVar_hsa_circ_50462,RMVar_hsa_circ_282182,RMVar_hsa_circ_46172,RMVar_hsa_circ_209512 49489 RMVar_ID_49489 Human_SNP_ID_679548288 A-to-I Human chr20 + 34437047 34437047 34437047 CCTACTCGGGAGGCTGAGGCATGAGAACTGCTAGAACCTGGTAGGTGAAGGTTGCAGTGAGCCGA CCTACTCGGGAGGCTGAGGCATGAGAACTGCTGGAACCTGGTAGGTGAAGGTTGCAGTGAGCCGA A G ITCH Ensembl:ENSG00000078747 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1424192609 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35941,RMVar_hsa_circ_70065,RMVar_hsa_circ_353174,RMVar_hsa_circ_42653,RMVar_hsa_circ_68688,RMVar_hsa_circ_73725,RMVar_hsa_circ_54559,RMVar_hsa_circ_2423,RMVar_hsa_circ_20385,RMVar_hsa_circ_15901,RMVar_hsa_circ_74558,RMVar_hsa_circ_303559,RMVar_hsa_circ_17294,RMVar_hsa_circ_345132,RMVar_hsa_circ_362008,RMVar_hsa_circ_352182,RMVar_hsa_circ_332425,RMVar_hsa_circ_342814,RMVar_hsa_circ_331034,RMVar_hsa_circ_298207,RMVar_hsa_circ_312079,RMVar_hsa_circ_317530,RMVar_hsa_circ_303750,RMVar_hsa_circ_50462,RMVar_hsa_circ_282182,RMVar_hsa_circ_46172,RMVar_hsa_circ_17754,RMVar_hsa_circ_305698,RMVar_hsa_circ_353253,RMVar_hsa_circ_358220,RMVar_hsa_circ_358804,RMVar_hsa_circ_329348,RMVar_hsa_circ_60168,RMVar_hsa_circ_74987,RMVar_hsa_circ_19776,RMVar_hsa_circ_1408 49490 RMVar_ID_49490 Human_SNP_ID_679550166 A-to-I Human chr20 + 34444397 34444397 34444397 CCTGAGGTCGGGAGTTCGAGGGCCGCCTGACCAACATGGAGAAACCCTGTCTCTACTAAAAATAC CCTGAGGTCGGGAGTTCGAGGGCCGCCTGACCGACATGGAGAAACCCTGTCTCTACTAAAAATAC A G ITCH Ensembl:ENSG00000078747 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1225275788 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70065,RMVar_hsa_circ_42653,RMVar_hsa_circ_68688,RMVar_hsa_circ_73725,RMVar_hsa_circ_54559,RMVar_hsa_circ_2423,RMVar_hsa_circ_5653,RMVar_hsa_circ_20385,RMVar_hsa_circ_15901,RMVar_hsa_circ_74558,RMVar_hsa_circ_17294,RMVar_hsa_circ_345132,RMVar_hsa_circ_332425,RMVar_hsa_circ_342814,RMVar_hsa_circ_331034,RMVar_hsa_circ_298207,RMVar_hsa_circ_312079,RMVar_hsa_circ_317530,RMVar_hsa_circ_50462,RMVar_hsa_circ_282182,RMVar_hsa_circ_46172,RMVar_hsa_circ_353253,RMVar_hsa_circ_358220,RMVar_hsa_circ_358804,RMVar_hsa_circ_329348,RMVar_hsa_circ_74987,RMVar_hsa_circ_19776,RMVar_hsa_circ_356201,RMVar_hsa_circ_369077,RMVar_hsa_circ_1408,RMVar_hsa_circ_372415,RMVar_hsa_circ_358228,RMVar_hsa_circ_340478,RMVar_hsa_circ_354448,RMVar_hsa_circ_65757,RMVar_hsa_circ_71827,RMVar_hsa_circ_56972,RMVar_hsa_circ_77839,RMVar_hsa_circ_324046,RMVar_hsa_circ_354989,RMVar_hsa_circ_209515,RMVar_hsa_circ_209516,RMVar_hsa_circ_209517,RMVar_hsa_circ_364296,RMVar_hsa_circ_326127,RMVar_hsa_circ_354901,RMVar_hsa_circ_302369,RMVar_hsa_circ_308316,RMVar_hsa_circ_209520,RMVar_hsa_circ_209522,RMVar_hsa_circ_209523,RMVar_hsa_circ_209521,RMVar_hsa_circ_336344,RMVar_hsa_circ_209518,RMVar_hsa_circ_209519,RMVar_hsa_circ_352832,RMVar_hsa_circ_375318,RMVar_hsa_circ_326708,RMVar_hsa_circ_329558,RMVar_hsa_circ_67127,RMVar_hsa_circ_209527,RMVar_hsa_circ_209528,RMVar_hsa_circ_209529,RMVar_hsa_circ_209526 49491 RMVar_ID_49491 Human_SNP_ID_679550184 A-to-I Human chr20 + 34444462 34444462 34444462 AAAATTAGCCAAGTGTGATGACGCATGCCTGTAATCACAGCTACTCAGGAGGCTGAGGCAGGAGA AAAATTAGCCAAGTGTGATGACGCATGCCTGTGATCACAGCTACTCAGGAGGCTGAGGCAGGAGA A G ITCH Ensembl:ENSG00000078747 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1568947914 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_70065,RMVar_hsa_circ_42653,RMVar_hsa_circ_68688,RMVar_hsa_circ_73725,RMVar_hsa_circ_54559,RMVar_hsa_circ_2423,RMVar_hsa_circ_5653,RMVar_hsa_circ_20385,RMVar_hsa_circ_15901,RMVar_hsa_circ_74558,RMVar_hsa_circ_17294,RMVar_hsa_circ_345132,RMVar_hsa_circ_332425,RMVar_hsa_circ_342814,RMVar_hsa_circ_331034,RMVar_hsa_circ_298207,RMVar_hsa_circ_312079,RMVar_hsa_circ_317530,RMVar_hsa_circ_50462,RMVar_hsa_circ_282182,RMVar_hsa_circ_46172,RMVar_hsa_circ_353253,RMVar_hsa_circ_358220,RMVar_hsa_circ_358804,RMVar_hsa_circ_329348,RMVar_hsa_circ_74987,RMVar_hsa_circ_19776,RMVar_hsa_circ_356201,RMVar_hsa_circ_369077,RMVar_hsa_circ_1408,RMVar_hsa_circ_372415,RMVar_hsa_circ_358228,RMVar_hsa_circ_340478,RMVar_hsa_circ_354448,RMVar_hsa_circ_65757,RMVar_hsa_circ_71827,RMVar_hsa_circ_56972,RMVar_hsa_circ_77839,RMVar_hsa_circ_324046,RMVar_hsa_circ_354989,RMVar_hsa_circ_209515,RMVar_hsa_circ_209516,RMVar_hsa_circ_209517,RMVar_hsa_circ_364296,RMVar_hsa_circ_326127,RMVar_hsa_circ_354901,RMVar_hsa_circ_302369,RMVar_hsa_circ_308316,RMVar_hsa_circ_209520,RMVar_hsa_circ_209522,RMVar_hsa_circ_209523,RMVar_hsa_circ_209521,RMVar_hsa_circ_336344,RMVar_hsa_circ_209518,RMVar_hsa_circ_209519,RMVar_hsa_circ_352832,RMVar_hsa_circ_375318,RMVar_hsa_circ_326708,RMVar_hsa_circ_329558,RMVar_hsa_circ_67127,RMVar_hsa_circ_209527,RMVar_hsa_circ_209528,RMVar_hsa_circ_209529,RMVar_hsa_circ_209526 49492 RMVar_ID_49492 Human_SNP_ID_679550334 A-to-I Human chr20 + 34444910 34444910 34444910 GTGATCCGCCTGCTTTGGCCTCCCAAAGTGCTAGGATCACAGGTGTGTGAGCCACTGCACCTGGC GTGATCCGCCTGCTTTGGCCTCCCAAAGTGCTGGGATCACAGGTGTGTGAGCCACTGCACCTGGC A G ITCH Ensembl:ENSG00000078747 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs905304730 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22600070 RMVar_hsa_circ_70065,RMVar_hsa_circ_42653,RMVar_hsa_circ_68688,RMVar_hsa_circ_73725,RMVar_hsa_circ_54559,RMVar_hsa_circ_2423,RMVar_hsa_circ_5653,RMVar_hsa_circ_20385,RMVar_hsa_circ_15901,RMVar_hsa_circ_74558,RMVar_hsa_circ_17294,RMVar_hsa_circ_345132,RMVar_hsa_circ_332425,RMVar_hsa_circ_342814,RMVar_hsa_circ_331034,RMVar_hsa_circ_298207,RMVar_hsa_circ_312079,RMVar_hsa_circ_317530,RMVar_hsa_circ_50462,RMVar_hsa_circ_282182,RMVar_hsa_circ_46172,RMVar_hsa_circ_353253,RMVar_hsa_circ_358220,RMVar_hsa_circ_358804,RMVar_hsa_circ_329348,RMVar_hsa_circ_74987,RMVar_hsa_circ_19776,RMVar_hsa_circ_356201,RMVar_hsa_circ_369077,RMVar_hsa_circ_1408,RMVar_hsa_circ_372415,RMVar_hsa_circ_358228,RMVar_hsa_circ_340478,RMVar_hsa_circ_354448,RMVar_hsa_circ_65757,RMVar_hsa_circ_71827,RMVar_hsa_circ_56972,RMVar_hsa_circ_77839,RMVar_hsa_circ_324046,RMVar_hsa_circ_354989,RMVar_hsa_circ_209515,RMVar_hsa_circ_209516,RMVar_hsa_circ_209517,RMVar_hsa_circ_364296,RMVar_hsa_circ_326127,RMVar_hsa_circ_354901,RMVar_hsa_circ_302369,RMVar_hsa_circ_308316,RMVar_hsa_circ_209520,RMVar_hsa_circ_209522,RMVar_hsa_circ_209523,RMVar_hsa_circ_209521,RMVar_hsa_circ_336344,RMVar_hsa_circ_209518,RMVar_hsa_circ_209519,RMVar_hsa_circ_352832,RMVar_hsa_circ_375318,RMVar_hsa_circ_326708,RMVar_hsa_circ_329558,RMVar_hsa_circ_67127,RMVar_hsa_circ_209527,RMVar_hsa_circ_209528,RMVar_hsa_circ_209529,RMVar_hsa_circ_209526 49493 RMVar_ID_49493 Human_SNP_ID_679552278 A-to-I Human chr20 + 34452756 34452756 34452756 GTGGCTGTTCTCCAGCATAGTAATTGCACACTACAGCTTTGAACTCCTGGCCTCAAGCAATGCCT GTGGCTGTTCTCCAGCATAGTAATTGCACACTGCAGCTTTGAACTCCTGGCCTCAAGCAATGCCT A G ITCH-IT1,ITCH Ensembl:ENSG00000231795,Ensembl:ENSG00000078747 lincRNA,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1198248845 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14077081 RMVar_hsa_circ_70065,RMVar_hsa_circ_68688,RMVar_hsa_circ_73725,RMVar_hsa_circ_2423,RMVar_hsa_circ_5653,RMVar_hsa_circ_20385,RMVar_hsa_circ_74558,RMVar_hsa_circ_17294,RMVar_hsa_circ_345132,RMVar_hsa_circ_332425,RMVar_hsa_circ_342814,RMVar_hsa_circ_331034,RMVar_hsa_circ_312079,RMVar_hsa_circ_317530,RMVar_hsa_circ_282182,RMVar_hsa_circ_46172,RMVar_hsa_circ_353253,RMVar_hsa_circ_358220,RMVar_hsa_circ_358804,RMVar_hsa_circ_329348,RMVar_hsa_circ_19776,RMVar_hsa_circ_356201,RMVar_hsa_circ_369077,RMVar_hsa_circ_1408,RMVar_hsa_circ_372415,RMVar_hsa_circ_340478,RMVar_hsa_circ_65757,RMVar_hsa_circ_71827,RMVar_hsa_circ_56972,RMVar_hsa_circ_77839,RMVar_hsa_circ_324046,RMVar_hsa_circ_354989,RMVar_hsa_circ_209516,RMVar_hsa_circ_209517,RMVar_hsa_circ_364296,RMVar_hsa_circ_326127,RMVar_hsa_circ_302369,RMVar_hsa_circ_209520,RMVar_hsa_circ_209522,RMVar_hsa_circ_209521,RMVar_hsa_circ_336344,RMVar_hsa_circ_209518,RMVar_hsa_circ_209519,RMVar_hsa_circ_352832,RMVar_hsa_circ_329558,RMVar_hsa_circ_67127,RMVar_hsa_circ_123584,RMVar_hsa_circ_209528,RMVar_hsa_circ_209529,RMVar_hsa_circ_69395,RMVar_hsa_circ_74368,RMVar_hsa_circ_209530 49494 RMVar_ID_49494 Human_SNP_ID_679552440 A-to-I Human chr20 + 34453536 34453536 34453536 GGAGGGTTGCTTGAGCCCCGGAGGTCAAGGCTATAGTGCGCTGTGATTGTATCACTGCACTCCAG GGAGGGTTGCTTGAGCCCCGGAGGTCAAGGCTGTAGTGCGCTGTGATTGTATCACTGCACTCCAG A G ITCH-IT1,ITCH Ensembl:ENSG00000231795,Ensembl:ENSG00000078747 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs533723456 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571516 RMVar_hsa_circ_70065,RMVar_hsa_circ_68688,RMVar_hsa_circ_73725,RMVar_hsa_circ_2423,RMVar_hsa_circ_5653,RMVar_hsa_circ_20385,RMVar_hsa_circ_74558,RMVar_hsa_circ_17294,RMVar_hsa_circ_345132,RMVar_hsa_circ_332425,RMVar_hsa_circ_342814,RMVar_hsa_circ_331034,RMVar_hsa_circ_312079,RMVar_hsa_circ_317530,RMVar_hsa_circ_282182,RMVar_hsa_circ_46172,RMVar_hsa_circ_353253,RMVar_hsa_circ_358220,RMVar_hsa_circ_358804,RMVar_hsa_circ_329348,RMVar_hsa_circ_19776,RMVar_hsa_circ_356201,RMVar_hsa_circ_369077,RMVar_hsa_circ_1408,RMVar_hsa_circ_372415,RMVar_hsa_circ_340478,RMVar_hsa_circ_65757,RMVar_hsa_circ_71827,RMVar_hsa_circ_56972,RMVar_hsa_circ_77839,RMVar_hsa_circ_324046,RMVar_hsa_circ_354989,RMVar_hsa_circ_209516,RMVar_hsa_circ_209517,RMVar_hsa_circ_364296,RMVar_hsa_circ_326127,RMVar_hsa_circ_302369,RMVar_hsa_circ_209520,RMVar_hsa_circ_209522,RMVar_hsa_circ_209521,RMVar_hsa_circ_336344,RMVar_hsa_circ_209518,RMVar_hsa_circ_209519,RMVar_hsa_circ_352832,RMVar_hsa_circ_329558,RMVar_hsa_circ_67127,RMVar_hsa_circ_123584,RMVar_hsa_circ_209528,RMVar_hsa_circ_209529,RMVar_hsa_circ_69395,RMVar_hsa_circ_74368,RMVar_hsa_circ_209530 49495 RMVar_ID_49495 Human_SNP_ID_679552441 A-to-I Human chr20 + 34453536 34453536 34453536 GGAGGGTTGCTTGAGCCCCGGAGGTCAAGGCTATAGTGCGCTGTGATTGTATCACTGCACTCCAG GGAGGGTTGCTTGAGCCCCGGAGGTCAAGGCTTTAGTGCGCTGTGATTGTATCACTGCACTCCAG A T ITCH-IT1,ITCH Ensembl:ENSG00000231795,Ensembl:ENSG00000078747 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs533723456 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571516 RMVar_hsa_circ_70065,RMVar_hsa_circ_68688,RMVar_hsa_circ_73725,RMVar_hsa_circ_2423,RMVar_hsa_circ_5653,RMVar_hsa_circ_20385,RMVar_hsa_circ_74558,RMVar_hsa_circ_17294,RMVar_hsa_circ_345132,RMVar_hsa_circ_332425,RMVar_hsa_circ_342814,RMVar_hsa_circ_331034,RMVar_hsa_circ_312079,RMVar_hsa_circ_317530,RMVar_hsa_circ_282182,RMVar_hsa_circ_46172,RMVar_hsa_circ_353253,RMVar_hsa_circ_358220,RMVar_hsa_circ_358804,RMVar_hsa_circ_329348,RMVar_hsa_circ_19776,RMVar_hsa_circ_356201,RMVar_hsa_circ_369077,RMVar_hsa_circ_1408,RMVar_hsa_circ_372415,RMVar_hsa_circ_340478,RMVar_hsa_circ_65757,RMVar_hsa_circ_71827,RMVar_hsa_circ_56972,RMVar_hsa_circ_77839,RMVar_hsa_circ_324046,RMVar_hsa_circ_354989,RMVar_hsa_circ_209516,RMVar_hsa_circ_209517,RMVar_hsa_circ_364296,RMVar_hsa_circ_326127,RMVar_hsa_circ_302369,RMVar_hsa_circ_209520,RMVar_hsa_circ_209522,RMVar_hsa_circ_209521,RMVar_hsa_circ_336344,RMVar_hsa_circ_209518,RMVar_hsa_circ_209519,RMVar_hsa_circ_352832,RMVar_hsa_circ_329558,RMVar_hsa_circ_67127,RMVar_hsa_circ_123584,RMVar_hsa_circ_209528,RMVar_hsa_circ_209529,RMVar_hsa_circ_69395,RMVar_hsa_circ_74368,RMVar_hsa_circ_209530 49496 RMVar_ID_49496 Human_SNP_ID_679556188 A-to-I Human chr20 + 34467365 34467365 34467365 AGCCTAGGCAACATGGTGAAACCCATGTCTACAAAAAATACAAAATATTAGCTGGGTGTGGTGGT AGCCTAGGCAACATGGTGAAACCCATGTCTACCAAAAATACAAAATATTAGCTGGGTGTGGTGGT A C ITCH Ensembl:ENSG00000078747 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1450166059 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_68688,RMVar_hsa_circ_73725,RMVar_hsa_circ_65265,RMVar_hsa_circ_20385,RMVar_hsa_circ_17294,RMVar_hsa_circ_345132,RMVar_hsa_circ_342814,RMVar_hsa_circ_312079,RMVar_hsa_circ_317530,RMVar_hsa_circ_282182,RMVar_hsa_circ_46172,RMVar_hsa_circ_358220,RMVar_hsa_circ_358804,RMVar_hsa_circ_329348,RMVar_hsa_circ_19776,RMVar_hsa_circ_369077,RMVar_hsa_circ_372415,RMVar_hsa_circ_340478,RMVar_hsa_circ_65757,RMVar_hsa_circ_71827,RMVar_hsa_circ_56972,RMVar_hsa_circ_77839,RMVar_hsa_circ_324046,RMVar_hsa_circ_209516,RMVar_hsa_circ_209517,RMVar_hsa_circ_364296,RMVar_hsa_circ_302369,RMVar_hsa_circ_209520,RMVar_hsa_circ_209518,RMVar_hsa_circ_209519,RMVar_hsa_circ_329558,RMVar_hsa_circ_67127,RMVar_hsa_circ_123584,RMVar_hsa_circ_209529,RMVar_hsa_circ_288591,RMVar_hsa_circ_209530,RMVar_hsa_circ_311040,RMVar_hsa_circ_362334,RMVar_hsa_circ_285039,RMVar_hsa_circ_285403,RMVar_hsa_circ_75133,RMVar_hsa_circ_209537,RMVar_hsa_circ_103259,RMVar_hsa_circ_209532,RMVar_hsa_circ_209534,RMVar_hsa_circ_209535,RMVar_hsa_circ_209533,RMVar_hsa_circ_209531,RMVar_hsa_circ_373459,RMVar_hsa_circ_39183,RMVar_hsa_circ_47238,RMVar_hsa_circ_8856,RMVar_hsa_circ_209536 49497 RMVar_ID_49497 Human_SNP_ID_679558692 A-to-I Human chr20 + 34476127 34476127 34476127 AACTTCTCATATATGTGATCTTCAAAGATGAGATGACAGGTTAAACAAGCCAGAGTTCCCTCACA AACTTCTCATATATGTGATCTTCAAAGATGAGGTGACAGGTTAAACAAGCCAGAGTTCCCTCACA A G ITCH Ensembl:ENSG00000078747 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs545186305 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73725,RMVar_hsa_circ_65265,RMVar_hsa_circ_20385,RMVar_hsa_circ_342814,RMVar_hsa_circ_312079,RMVar_hsa_circ_317530,RMVar_hsa_circ_46172,RMVar_hsa_circ_358220,RMVar_hsa_circ_19776,RMVar_hsa_circ_369077,RMVar_hsa_circ_340478,RMVar_hsa_circ_65757,RMVar_hsa_circ_56972,RMVar_hsa_circ_77839,RMVar_hsa_circ_209517,RMVar_hsa_circ_364296,RMVar_hsa_circ_209518,RMVar_hsa_circ_209519,RMVar_hsa_circ_123584,RMVar_hsa_circ_209529,RMVar_hsa_circ_209530,RMVar_hsa_circ_311040,RMVar_hsa_circ_362334,RMVar_hsa_circ_285039,RMVar_hsa_circ_75133,RMVar_hsa_circ_209543,RMVar_hsa_circ_209537,RMVar_hsa_circ_103259,RMVar_hsa_circ_209532,RMVar_hsa_circ_209533,RMVar_hsa_circ_209531,RMVar_hsa_circ_39183,RMVar_hsa_circ_8856,RMVar_hsa_circ_25229,RMVar_hsa_circ_274201,RMVar_hsa_circ_359105,RMVar_hsa_circ_300819,RMVar_hsa_circ_285273,RMVar_hsa_circ_271855,RMVar_hsa_circ_277290,RMVar_hsa_circ_209540,RMVar_hsa_circ_209541,RMVar_hsa_circ_209539,RMVar_hsa_circ_329670,RMVar_hsa_circ_333474,RMVar_hsa_circ_315352,RMVar_hsa_circ_209545,RMVar_hsa_circ_66296,RMVar_hsa_circ_209544,RMVar_hsa_circ_209542 49498 RMVar_ID_49498 Human_SNP_ID_679558694 A-to-I Human chr20 + 34476137 34476137 34476137 ATATGTGATCTTCAAAGATGAGATGACAGGTTAAACAAGCCAGAGTTCCCTCACATGCACCAAAG ATATGTGATCTTCAAAGATGAGATGACAGGTTGAACAAGCCAGAGTTCCCTCACATGCACCAAAG A G ITCH Ensembl:ENSG00000078747 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs572085948 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73725,RMVar_hsa_circ_65265,RMVar_hsa_circ_20385,RMVar_hsa_circ_342814,RMVar_hsa_circ_312079,RMVar_hsa_circ_317530,RMVar_hsa_circ_46172,RMVar_hsa_circ_358220,RMVar_hsa_circ_19776,RMVar_hsa_circ_369077,RMVar_hsa_circ_340478,RMVar_hsa_circ_65757,RMVar_hsa_circ_56972,RMVar_hsa_circ_77839,RMVar_hsa_circ_209517,RMVar_hsa_circ_364296,RMVar_hsa_circ_209518,RMVar_hsa_circ_209519,RMVar_hsa_circ_123584,RMVar_hsa_circ_209529,RMVar_hsa_circ_209530,RMVar_hsa_circ_311040,RMVar_hsa_circ_362334,RMVar_hsa_circ_285039,RMVar_hsa_circ_75133,RMVar_hsa_circ_209543,RMVar_hsa_circ_209537,RMVar_hsa_circ_103259,RMVar_hsa_circ_209532,RMVar_hsa_circ_209533,RMVar_hsa_circ_209531,RMVar_hsa_circ_39183,RMVar_hsa_circ_8856,RMVar_hsa_circ_25229,RMVar_hsa_circ_274201,RMVar_hsa_circ_359105,RMVar_hsa_circ_300819,RMVar_hsa_circ_285273,RMVar_hsa_circ_271855,RMVar_hsa_circ_277290,RMVar_hsa_circ_209540,RMVar_hsa_circ_209541,RMVar_hsa_circ_209539,RMVar_hsa_circ_329670,RMVar_hsa_circ_333474,RMVar_hsa_circ_315352,RMVar_hsa_circ_209545,RMVar_hsa_circ_66296,RMVar_hsa_circ_209544,RMVar_hsa_circ_209542 49499 RMVar_ID_49499 Human_SNP_ID_679558695 A-to-I Human chr20 + 34476137 34476137 34476137 ATATGTGATCTTCAAAGATGAGATGACAGGTTAAACAAGCCAGAGTTCCCTCACATGCACCAAAG ATATGTGATCTTCAAAGATGAGATGACAGGTTTAACAAGCCAGAGTTCCCTCACATGCACCAAAG A T ITCH Ensembl:ENSG00000078747 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs572085948 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73725,RMVar_hsa_circ_65265,RMVar_hsa_circ_20385,RMVar_hsa_circ_342814,RMVar_hsa_circ_312079,RMVar_hsa_circ_317530,RMVar_hsa_circ_46172,RMVar_hsa_circ_358220,RMVar_hsa_circ_19776,RMVar_hsa_circ_369077,RMVar_hsa_circ_340478,RMVar_hsa_circ_65757,RMVar_hsa_circ_56972,RMVar_hsa_circ_77839,RMVar_hsa_circ_209517,RMVar_hsa_circ_364296,RMVar_hsa_circ_209518,RMVar_hsa_circ_209519,RMVar_hsa_circ_123584,RMVar_hsa_circ_209529,RMVar_hsa_circ_209530,RMVar_hsa_circ_311040,RMVar_hsa_circ_362334,RMVar_hsa_circ_285039,RMVar_hsa_circ_75133,RMVar_hsa_circ_209543,RMVar_hsa_circ_209537,RMVar_hsa_circ_103259,RMVar_hsa_circ_209532,RMVar_hsa_circ_209533,RMVar_hsa_circ_209531,RMVar_hsa_circ_39183,RMVar_hsa_circ_8856,RMVar_hsa_circ_25229,RMVar_hsa_circ_274201,RMVar_hsa_circ_359105,RMVar_hsa_circ_300819,RMVar_hsa_circ_285273,RMVar_hsa_circ_271855,RMVar_hsa_circ_277290,RMVar_hsa_circ_209540,RMVar_hsa_circ_209541,RMVar_hsa_circ_209539,RMVar_hsa_circ_329670,RMVar_hsa_circ_333474,RMVar_hsa_circ_315352,RMVar_hsa_circ_209545,RMVar_hsa_circ_66296,RMVar_hsa_circ_209544,RMVar_hsa_circ_209542 49500 RMVar_ID_49500 Human_SNP_ID_679558698 A-to-I Human chr20 + 34476148 34476148 34476148 TCAAAGATGAGATGACAGGTTAAACAAGCCAGAGTTCCCTCACATGCACCAAAGCCATCAATATC TCAAAGATGAGATGACAGGTTAAACAAGCCAGGGTTCCCTCACATGCACCAAAGCCATCAATATC A G ITCH Ensembl:ENSG00000078747 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs542643642 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73725,RMVar_hsa_circ_65265,RMVar_hsa_circ_20385,RMVar_hsa_circ_342814,RMVar_hsa_circ_312079,RMVar_hsa_circ_317530,RMVar_hsa_circ_46172,RMVar_hsa_circ_358220,RMVar_hsa_circ_19776,RMVar_hsa_circ_369077,RMVar_hsa_circ_340478,RMVar_hsa_circ_65757,RMVar_hsa_circ_56972,RMVar_hsa_circ_77839,RMVar_hsa_circ_209517,RMVar_hsa_circ_364296,RMVar_hsa_circ_209518,RMVar_hsa_circ_209519,RMVar_hsa_circ_123584,RMVar_hsa_circ_209529,RMVar_hsa_circ_209530,RMVar_hsa_circ_311040,RMVar_hsa_circ_362334,RMVar_hsa_circ_285039,RMVar_hsa_circ_75133,RMVar_hsa_circ_209543,RMVar_hsa_circ_209537,RMVar_hsa_circ_103259,RMVar_hsa_circ_209532,RMVar_hsa_circ_209533,RMVar_hsa_circ_209531,RMVar_hsa_circ_39183,RMVar_hsa_circ_8856,RMVar_hsa_circ_25229,RMVar_hsa_circ_274201,RMVar_hsa_circ_359105,RMVar_hsa_circ_300819,RMVar_hsa_circ_285273,RMVar_hsa_circ_271855,RMVar_hsa_circ_277290,RMVar_hsa_circ_209540,RMVar_hsa_circ_209541,RMVar_hsa_circ_209539,RMVar_hsa_circ_329670,RMVar_hsa_circ_333474,RMVar_hsa_circ_315352,RMVar_hsa_circ_209545,RMVar_hsa_circ_66296,RMVar_hsa_circ_209544,RMVar_hsa_circ_209542 49501 RMVar_ID_49501 Human_SNP_ID_679561084 A-to-I Human chr20 + 34485783 34485783 34485783 GAGCTCACTGCAGTCTTAAACTCCTGGGATCAAAGGATCCCCCTGCCTCATCCTTCTGAGTAGCT GAGCTCACTGCAGTCTTAAACTCCTGGGATCAGAGGATCCCCCTGCCTCATCCTTCTGAGTAGCT A G ITCH Ensembl:ENSG00000078747 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs868725145 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73725,RMVar_hsa_circ_20385,RMVar_hsa_circ_342814,RMVar_hsa_circ_317530,RMVar_hsa_circ_19776,RMVar_hsa_circ_340478,RMVar_hsa_circ_65757,RMVar_hsa_circ_209517,RMVar_hsa_circ_123584,RMVar_hsa_circ_209529,RMVar_hsa_circ_209530,RMVar_hsa_circ_311040,RMVar_hsa_circ_362334,RMVar_hsa_circ_75133,RMVar_hsa_circ_209537,RMVar_hsa_circ_103259,RMVar_hsa_circ_209532,RMVar_hsa_circ_209531,RMVar_hsa_circ_39183,RMVar_hsa_circ_274201,RMVar_hsa_circ_300819,RMVar_hsa_circ_285273,RMVar_hsa_circ_209540,RMVar_hsa_circ_209541,RMVar_hsa_circ_333474,RMVar_hsa_circ_315352,RMVar_hsa_circ_209545,RMVar_hsa_circ_209544,RMVar_hsa_circ_209553,RMVar_hsa_circ_121215,RMVar_hsa_circ_360906,RMVar_hsa_circ_71995,RMVar_hsa_circ_209547,RMVar_hsa_circ_209546,RMVar_hsa_circ_103848,RMVar_hsa_circ_364301,RMVar_hsa_circ_73586 49502 RMVar_ID_49502 Human_SNP_ID_679580364 A-to-I Human chr20 + 34561134 34561134 34561134 ACTGGAGAGGCCCTCCTCAGGGCCCCCACCTCAGGGCCCATAATTGACCCTGCAAGGTCTGGCCT ACTGGAGAGGCCCTCCTCAGGGCCCCCACCTCGGGGCCCATAATTGACCCTGCAAGGTCTGGCCT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs536985208 Functional Loss SNV dbSNP153 33..33 33 - - - 49503 RMVar_ID_49503 Human_SNP_ID_679585037 A-to-I Human chr20 - 34582497 34582497 34582497 TTTTAAATTTTTTGTAGAGATGAGATTTCACTATGTTGCCTAGGCTGGTCTCAAACTCCTGGGCT TTTTAAATTTTTTGTAGAGATGAGATTTCACTGTGTTGCCTAGGCTGGTCTCAAACTCCTGGGCT T C PIGU Ensembl:ENSG00000101464 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1241990302 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78899,RMVar_hsa_circ_107662,RMVar_hsa_circ_114865,RMVar_hsa_circ_104892,RMVar_hsa_circ_96280,RMVar_hsa_circ_209566,RMVar_hsa_circ_209567,RMVar_hsa_circ_209568,RMVar_hsa_circ_209565,RMVar_hsa_circ_209571,RMVar_hsa_circ_282151,RMVar_hsa_circ_306579,RMVar_hsa_circ_209569,RMVar_hsa_circ_29361,RMVar_hsa_circ_37979,RMVar_hsa_circ_23703,RMVar_hsa_circ_209573,RMVar_hsa_circ_323744,RMVar_hsa_circ_209570,RMVar_hsa_circ_348937,RMVar_hsa_circ_289895 49504 RMVar_ID_49504 Human_SNP_ID_679625875 A-to-I Human chr20 - 34751996 34751996 34751996 AAAATTAGCCGGGTGTGTTGTTGTGCGCTTCTAGTTTCAGCTACTGGGGAGGCTGAGGCATGAAA AAAATTAGCCGGGTGTGTTGTTGTGCGCTTCTGGTTTCAGCTACTGGGGAGGCTGAGGCATGAAA T C NCOA6 Ensembl:ENSG00000198646 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1490241251 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_263,RMVar_hsa_circ_366395,RMVar_hsa_circ_72801,RMVar_hsa_circ_347024 49505 RMVar_ID_49505 Human_SNP_ID_679626174 A-to-I Human chr20 - 34753250 34753250 34753250 TTGAGATCATGAGTTTGAGACCATCCTGACCAACGTGGTAAAACCCTGTCTCTACTAAAAATACA TTGAGATCATGAGTTTGAGACCATCCTGACCAGCGTGGTAAAACCCTGTCTCTACTAAAAATACA T C NCOA6 Ensembl:ENSG00000198646 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs554281364 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_263,RMVar_hsa_circ_366395,RMVar_hsa_circ_72801,RMVar_hsa_circ_347024 49506 RMVar_ID_49506 Human_SNP_ID_679630560 A-to-I Human chr20 - 34772104 34772104 34772104 TGTCGCTAGTCTTGAACTCCTGGTCTGAAGCAATCCTCCCACCTTGGCCTCCCAAAGTGCTGGGA TGTCGCTAGTCTTGAACTCCTGGTCTGAAGCAGTCCTCCCACCTTGGCCTCCCAAAGTGCTGGGA T C NCOA6 Ensembl:ENSG00000198646 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs200033099 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72801,RMVar_hsa_circ_12372,RMVar_hsa_circ_349530,RMVar_hsa_circ_20796,RMVar_hsa_circ_44309,RMVar_hsa_circ_359493,RMVar_hsa_circ_319228,RMVar_hsa_circ_279644,RMVar_hsa_circ_209595 49507 RMVar_ID_49507 Human_SNP_ID_679630565 A-to-I Human chr20 - 34772129 34772129 34772129 TTTTTATAGAGACGGGGTCTCACCATGTCGCTAGTCTTGAACTCCTGGTCTGAAGCAATCCTCCC TTTTTATAGAGACGGGGTCTCACCATGTCGCTGGTCTTGAACTCCTGGTCTGAAGCAATCCTCCC T C NCOA6 Ensembl:ENSG00000198646 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041861511 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72801,RMVar_hsa_circ_12372,RMVar_hsa_circ_349530,RMVar_hsa_circ_20796,RMVar_hsa_circ_44309,RMVar_hsa_circ_359493,RMVar_hsa_circ_319228,RMVar_hsa_circ_279644,RMVar_hsa_circ_209595 49508 RMVar_ID_49508 Human_SNP_ID_679631923 A-to-I Human chr20 - 34777380 34777380 34777380 GAACTCCTGTCCTCAAGTGATCCACCAGCCTCAGCCTCCCAAAGTGCTGGGATTATTGGGATTAT GAACTCCTGTCCTCAAGTGATCCACCAGCCTCGGCCTCCCAAAGTGCTGGGATTATTGGGATTAT T C NCOA6 Ensembl:ENSG00000198646 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1359919324 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_72801,RMVar_hsa_circ_12372,RMVar_hsa_circ_31450,RMVar_hsa_circ_20796,RMVar_hsa_circ_359493,RMVar_hsa_circ_319228,RMVar_hsa_circ_280889,RMVar_hsa_circ_209597 49509 RMVar_ID_49509 Human_SNP_ID_679636294 A-to-I Human chr20 - 34796500 34796500 34796500 CTCTCACCTCAGCCTTCTGAGTAGCTGGGACTACAGGCACACACTACCACACCTAGCTAATTTTT CTCTCACCTCAGCCTTCTGAGTAGCTGGGACTGCAGGCACACACTACCACACCTAGCTAATTTTT T C NCOA6 Ensembl:ENSG00000198646 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs949411044 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_357412,RMVar_hsa_circ_209599,RMVar_hsa_circ_209600,RMVar_hsa_circ_296791 49510 RMVar_ID_49510 Human_SNP_ID_679640443 A-to-I Human chr20 - 34814204 34814204 34814204 CTCCTGAGTAGCTAGGATTACAGGCATGCGCCACCATGCCTGGCTAATTTTTGTATTTTCACGGG CTCCTGAGTAGCTAGGATTACAGGCATGCGCCGCCATGCCTGGCTAATTTTTGTATTTTCACGGG T C NCOA6 Ensembl:ENSG00000198646 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1236616952 Functional Loss SNV dbSNP153 33..33 33 - - - 49511 RMVar_ID_49511 Human_SNP_ID_679647571 A-to-I Human chr20 - 34844888 34844888 34844888 CTCCCATTCCCAGCCTCATTTCTTAAATGACTAGGAATTTTTTAATGGACCATCATAGGGAGGGG CTCCCATTCCCAGCCTCATTTCTTAAATGACTGGGAATTTTTTAATGGACCATCATAGGGAGGGG T C GGT7 Ensembl:ENSG00000131067 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1328141111 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_562302,Human_RBP_ID_14080153,Human_RBP_ID_17063877 49512 RMVar_ID_49512 Human_SNP_ID_679652287 A-to-I Human chr20 - 34863463 34863463 34863463 TCGGAGATGGGCAGCCAAGACGGGTCGCCGCTACGCGAGACGCGCAAAGACCCGTTCTCCGCCGC TCGGAGATGGGCAGCCAAGACGGGTCGCCGCTGCGCGAGACGCGCAAAGACCCGTTCTCCGCCGC T C GGT7 Ensembl:ENSG00000131067 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1479361034 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4642992,Human_RBP_ID_9390389,Human_RBP_ID_22453036,Human_RBP_ID_23115448 Human_Splice_Rec_2074606,Human_Splice_Rec_2074650 Human_miRNA_ID_2158167 RMVar_hsa_circ_100195,RMVar_hsa_circ_209610 49513 RMVar_ID_49513 Human_SNP_ID_679657086 A-to-I Human chr20 + 34884075 34884075 34884075 TCAAGCAATCCTGCCACCTCAGCCTCCTGAGTAGGTGGGACTACAGACATGCACCACCACGTTTG TCAAGCAATCCTGCCACCTCAGCCTCCTGAGTGGGTGGGACTACAGACATGCACCACCACGTTTG A G ACSS2 Ensembl:ENSG00000131069 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs909957096 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7331 49514 RMVar_ID_49514 Human_SNP_ID_679657224 A-to-I Human chr20 + 34884812 34884812 34884812 CGGGCATGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAAGAGGGTTGCTTGA CGGGCATGGTGGCTCATGCCTGTAATCCCAGCCCTTTGGGAGGCTGAGGCAAGAGGGTTGCTTGA A C ACSS2 Ensembl:ENSG00000131069 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1357751038 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7331 49515 RMVar_ID_49515 Human_SNP_ID_679661364 A-to-I Human chr20 + 34902971 34902971 34902971 CCCAGTCTGGTCTCGAACTCTTGGGCTCAAGCAATCCTCCCACCTTGGCTTCCCAAAATGCTGGG CCCAGTCTGGTCTCGAACTCTTGGGCTCAAGCGATCCTCCCACCTTGGCTTCCCAAAATGCTGGG A G ACSS2 Ensembl:ENSG00000131069 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1205892726 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22479111 RMVar_hsa_circ_7331 49516 RMVar_ID_49516 Human_SNP_ID_679662644 A-to-I Human chr20 + 34908740 34908740 34908740 AAAATTAGCCAGGTGTGGTGGTGCACGCCTGTAATCCCAGCTACTCAGGAGTCTGAGGCAGAAGA AAAATTAGCCAGGTGTGGTGGTGCACGCCTGTGATCCCAGCTACTCAGGAGTCTGAGGCAGAAGA A G ACSS2 Ensembl:ENSG00000131069 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444692249 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2074666 RMVar_hsa_circ_7331 49517 RMVar_ID_49517 Human_SNP_ID_679683649 A-to-I Human chr20 - 34992734 34992734 34992734 GAAACCCTATCTCTACTAAAAACACAAAAATTAGTGGGGCATGGTGGCGGGCGCCTGTAATCCCA GAAACCCTATCTCTACTAAAAACACAAAAATTGGTGGGGCATGGTGGCGGGCGCCTGTAATCCCA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1426458926 Functional Loss SNV dbSNP153 33..33 33 - - - 49518 RMVar_ID_49518 Human_SNP_ID_679693596 A-to-I Human chr20 - 35024605 35024605 35024605 TGCCCAAGCTGGTCTCAAACTCCTGCACTCAAATGATCTTCCCGTCTTGGTCTTCCAAAGTGCCG TGCCCAAGCTGGTCTCAAACTCCTGCACTCAAGTGATCTTCCCGTCTTGGTCTTCCAAAGTGCCG T C TRPC4AP Ensembl:ENSG00000100991 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1272162181 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101021,RMVar_hsa_circ_209624,RMVar_hsa_circ_63308,RMVar_hsa_circ_209627,RMVar_hsa_circ_350157,RMVar_hsa_circ_95426,RMVar_hsa_circ_107572,RMVar_hsa_circ_123370,RMVar_hsa_circ_79589,RMVar_hsa_circ_87252,RMVar_hsa_circ_209634,RMVar_hsa_circ_209635,RMVar_hsa_circ_209636,RMVar_hsa_circ_209633,RMVar_hsa_circ_99933,RMVar_hsa_circ_209637,RMVar_hsa_circ_209638,RMVar_hsa_circ_20159,RMVar_hsa_circ_283134,RMVar_hsa_circ_340259,RMVar_hsa_circ_209639 49519 RMVar_ID_49519 Human_SNP_ID_679693873 A-to-I Human chr20 - 35025319 35025319 35025319 TCGGTTAGCCAGGCATGGTGGCACGTGCCCATAGTCCTGACAACTTGGGAGGCTGAGGTGGGAGG TCGGTTAGCCAGGCATGGTGGCACGTGCCCATGGTCCTGACAACTTGGGAGGCTGAGGTGGGAGG T C TRPC4AP Ensembl:ENSG00000100991 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs770566055 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101021,RMVar_hsa_circ_209624,RMVar_hsa_circ_63308,RMVar_hsa_circ_209627,RMVar_hsa_circ_350157,RMVar_hsa_circ_95426,RMVar_hsa_circ_107572,RMVar_hsa_circ_123370,RMVar_hsa_circ_79589,RMVar_hsa_circ_87252,RMVar_hsa_circ_209634,RMVar_hsa_circ_209635,RMVar_hsa_circ_209636,RMVar_hsa_circ_209633,RMVar_hsa_circ_99933,RMVar_hsa_circ_209637,RMVar_hsa_circ_209638,RMVar_hsa_circ_20159,RMVar_hsa_circ_283134,RMVar_hsa_circ_340259,RMVar_hsa_circ_209639 49520 RMVar_ID_49520 Human_SNP_ID_679695164 A-to-I Human chr20 - 35030146 35030146 35030146 ACCTCCGCCTCCTGGGTTCAAGTGATTCCCCTACCTCAGCCTCTCTAGTAGCTGGGATTACAGGC ACCTCCGCCTCCTGGGTTCAAGTGATTCCCCTGCCTCAGCCTCTCTAGTAGCTGGGATTACAGGC T C TRPC4AP Ensembl:ENSG00000100991 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs555553009 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101021,RMVar_hsa_circ_209624,RMVar_hsa_circ_63308,RMVar_hsa_circ_209627,RMVar_hsa_circ_350157,RMVar_hsa_circ_95426,RMVar_hsa_circ_107572,RMVar_hsa_circ_123370,RMVar_hsa_circ_79589,RMVar_hsa_circ_87252,RMVar_hsa_circ_209634,RMVar_hsa_circ_209635,RMVar_hsa_circ_209636,RMVar_hsa_circ_209633,RMVar_hsa_circ_99933,RMVar_hsa_circ_209637,RMVar_hsa_circ_209638,RMVar_hsa_circ_20159,RMVar_hsa_circ_283134,RMVar_hsa_circ_340259,RMVar_hsa_circ_209639 49521 RMVar_ID_49521 Human_SNP_ID_679695961 A-to-I Human chr20 - 35032986 35032986 35032986 TACCTAGTTGCTGGTATTGAACTCCTGAGCTCAGGCAATCCACCCACCTTGGCCTCCCAAAGTGC TACCTAGTTGCTGGTATTGAACTCCTGAGCTCGGGCAATCCACCCACCTTGGCCTCCCAAAGTGC T C TRPC4AP Ensembl:ENSG00000100991 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs369485330 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571537 RMVar_hsa_circ_101021,RMVar_hsa_circ_209624,RMVar_hsa_circ_63308,RMVar_hsa_circ_209627,RMVar_hsa_circ_350157,RMVar_hsa_circ_95426,RMVar_hsa_circ_107572,RMVar_hsa_circ_123370,RMVar_hsa_circ_79589,RMVar_hsa_circ_87252,RMVar_hsa_circ_209634,RMVar_hsa_circ_209635,RMVar_hsa_circ_209636,RMVar_hsa_circ_209633,RMVar_hsa_circ_99933,RMVar_hsa_circ_209637,RMVar_hsa_circ_209638,RMVar_hsa_circ_20159,RMVar_hsa_circ_283134,RMVar_hsa_circ_340259,RMVar_hsa_circ_209639 49522 RMVar_ID_49522 Human_SNP_ID_679695971 A-to-I Human chr20 - 35033034 35033034 35033034 TGCCACCACACCCGGCTAATTTTTTGTATTTTAGTAGAGAAAGGATTTTACCTAGTTGCTGGTAT TGCCACCACACCCGGCTAATTTTTTGTATTTTGGTAGAGAAAGGATTTTACCTAGTTGCTGGTAT T C TRPC4AP Ensembl:ENSG00000100991 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1307298030 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101021,RMVar_hsa_circ_209624,RMVar_hsa_circ_63308,RMVar_hsa_circ_209627,RMVar_hsa_circ_350157,RMVar_hsa_circ_95426,RMVar_hsa_circ_107572,RMVar_hsa_circ_123370,RMVar_hsa_circ_79589,RMVar_hsa_circ_87252,RMVar_hsa_circ_209634,RMVar_hsa_circ_209635,RMVar_hsa_circ_209636,RMVar_hsa_circ_209633,RMVar_hsa_circ_99933,RMVar_hsa_circ_209637,RMVar_hsa_circ_209638,RMVar_hsa_circ_20159,RMVar_hsa_circ_283134,RMVar_hsa_circ_340259,RMVar_hsa_circ_209639 49523 RMVar_ID_49523 Human_SNP_ID_679695972 A-to-I Human chr20 - 35033034 35033034 35033034 TGCCACCACACCCGGCTAATTTTTTGTATTTTAGTAGAGAAAGGATTTTACCTAGTTGCTGGTAT TGCCACCACACCCGGCTAATTTTTTGTATTTTCGTAGAGAAAGGATTTTACCTAGTTGCTGGTAT T G TRPC4AP Ensembl:ENSG00000100991 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1307298030 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101021,RMVar_hsa_circ_209624,RMVar_hsa_circ_63308,RMVar_hsa_circ_209627,RMVar_hsa_circ_350157,RMVar_hsa_circ_95426,RMVar_hsa_circ_107572,RMVar_hsa_circ_123370,RMVar_hsa_circ_79589,RMVar_hsa_circ_87252,RMVar_hsa_circ_209634,RMVar_hsa_circ_209635,RMVar_hsa_circ_209636,RMVar_hsa_circ_209633,RMVar_hsa_circ_99933,RMVar_hsa_circ_209637,RMVar_hsa_circ_209638,RMVar_hsa_circ_20159,RMVar_hsa_circ_283134,RMVar_hsa_circ_340259,RMVar_hsa_circ_209639 49524 RMVar_ID_49524 Human_SNP_ID_679695989 A-to-I Human chr20 - 35033075 35033075 35033075 GTTCTCTCTCAGCCTCCCGAGTAGCTGGGGTTACAGGTGCATGCCACCACACCCGGCTAATTTTT GTTCTCTCTCAGCCTCCCGAGTAGCTGGGGTTGCAGGTGCATGCCACCACACCCGGCTAATTTTT T C TRPC4AP Ensembl:ENSG00000100991 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1236874907 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101021,RMVar_hsa_circ_209624,RMVar_hsa_circ_63308,RMVar_hsa_circ_209627,RMVar_hsa_circ_350157,RMVar_hsa_circ_95426,RMVar_hsa_circ_107572,RMVar_hsa_circ_123370,RMVar_hsa_circ_79589,RMVar_hsa_circ_87252,RMVar_hsa_circ_209634,RMVar_hsa_circ_209635,RMVar_hsa_circ_209636,RMVar_hsa_circ_209633,RMVar_hsa_circ_99933,RMVar_hsa_circ_209637,RMVar_hsa_circ_209638,RMVar_hsa_circ_20159,RMVar_hsa_circ_283134,RMVar_hsa_circ_340259,RMVar_hsa_circ_209639 49525 RMVar_ID_49525 Human_SNP_ID_679696006 A-to-I Human chr20 - 35033147 35033147 35033147 TCTTGTCGCCCAGGTTGGAGGGCAGTGGCACAATCTCGGCTCACTGCAACCTCTGTCTCCCATGT TCTTGTCGCCCAGGTTGGAGGGCAGTGGCACAGTCTCGGCTCACTGCAACCTCTGTCTCCCATGT T C TRPC4AP Ensembl:ENSG00000100991 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs373685367 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101021,RMVar_hsa_circ_209624,RMVar_hsa_circ_63308,RMVar_hsa_circ_209627,RMVar_hsa_circ_350157,RMVar_hsa_circ_95426,RMVar_hsa_circ_107572,RMVar_hsa_circ_123370,RMVar_hsa_circ_79589,RMVar_hsa_circ_87252,RMVar_hsa_circ_209634,RMVar_hsa_circ_209635,RMVar_hsa_circ_209636,RMVar_hsa_circ_209633,RMVar_hsa_circ_99933,RMVar_hsa_circ_209637,RMVar_hsa_circ_209638,RMVar_hsa_circ_20159,RMVar_hsa_circ_283134,RMVar_hsa_circ_340259,RMVar_hsa_circ_209639 49526 RMVar_ID_49526 Human_SNP_ID_679696138 A-to-I Human chr20 - 35033766 35033766 35033766 GCTGGTCTCAAACTCCTGGCCTCAAGTGATCCACCCTCCTTGGCCTCCCAGAGTGCCAGGTTTAT GCTGGTCTCAAACTCCTGGCCTCAAGTGATCCGCCCTCCTTGGCCTCCCAGAGTGCCAGGTTTAT T C TRPC4AP Ensembl:ENSG00000100991 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1426478243 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25605031 RMVar_hsa_circ_101021,RMVar_hsa_circ_209624,RMVar_hsa_circ_63308,RMVar_hsa_circ_209627,RMVar_hsa_circ_350157,RMVar_hsa_circ_95426,RMVar_hsa_circ_107572,RMVar_hsa_circ_123370,RMVar_hsa_circ_79589,RMVar_hsa_circ_87252,RMVar_hsa_circ_209634,RMVar_hsa_circ_209635,RMVar_hsa_circ_209636,RMVar_hsa_circ_209633,RMVar_hsa_circ_99933,RMVar_hsa_circ_209637,RMVar_hsa_circ_209638,RMVar_hsa_circ_20159,RMVar_hsa_circ_283134,RMVar_hsa_circ_340259,RMVar_hsa_circ_209639 49527 RMVar_ID_49527 Human_SNP_ID_679725251 A-to-I Human chr20 - 35141870 35141870 35141870 TTTAATGATATTAAATTTAAGTAGTCACATGTAGTTAGTGATTATTGTATTGGACAGTGCAAATC TTTAATGATATTAAATTTAAGTAGTCACATGTGGTTAGTGATTATTGTATTGGACAGTGCAAATC T C EDEM2 Ensembl:ENSG00000088298 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1228304182 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4869,RMVar_hsa_circ_117137,RMVar_hsa_circ_114291,RMVar_hsa_circ_209656,RMVar_hsa_circ_338806,RMVar_hsa_circ_209657 49528 RMVar_ID_49528 Human_SNP_ID_679735802 A-to-I Human chr20 + 35182902 35182902 35182902 AGGCTAAGGAAGGAGAGTAGCTTGCACCCAGGAGGCAGATGTTGCAGTGAGTTGAGATCGTGCCA AGGCTAAGGAAGGAGAGTAGCTTGCACCCAGGTGGCAGATGTTGCAGTGAGTTGAGATCGTGCCA A T PROCR Ensembl:ENSG00000101000 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027999483 Functional Loss SNV dbSNP153 33..33 33 - - - 49529 RMVar_ID_49529 Human_SNP_ID_679756887 A-to-I Human chr20 - 35273313 35273313 35273313 TAACTCACTGCAGCCTCAAACTCCTGGTCTTAAGCAATCCTCTGGCCTCAGCCTCCCAAGTAGCT TAACTCACTGCAGCCTCAAACTCCTGGTCTTAGGCAATCCTCTGGCCTCAGCCTCCCAAGTAGCT T C AL121753.1,MMP24OS Ensembl:ENSG00000261582,Ensembl:ENSG00000126005 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1323834322 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2682447,Human_RBP_ID_14081938 49530 RMVar_ID_49530 Human_SNP_ID_679759056 A-to-I Human chr20 - 35280740 35280740 35280740 TTCGCAACAGCCTCCCAGACACAGTGCAGATTAGGCGGGTGGAGGAGCGGCTCTCAGCCTTGGGC TTCGCAACAGCCTCCCAGACACAGTGCAGATTTGGCGGGTGGAGGAGCGGCTCTCAGCCTTGGGC T A EIF6 Ensembl:ENSG00000242372 Protein coding intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1203096104 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4643405,Human_RBP_ID_14082062,Human_RBP_ID_22506461 Human_Splice_Rec_2075722,Human_Splice_Rec_2075723,Human_Splice_Rec_2075752,Human_Splice_Rec_2075753,Human_Splice_Rec_2075762,Human_Splice_Rec_2075763,Human_Splice_Rec_2075776 RMVar_hsa_circ_119764,RMVar_hsa_circ_95804,RMVar_hsa_circ_103158,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_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 49531 RMVar_ID_49531 Human_SNP_ID_679759325 A-to-I Human chr20 - 35281650 35281650 35281650 CCTGAGGTTAGGAGTTCGAGACCAGCCTGGCCAACATAGTGAGACCCCATCTCTACAAAATCACA CCTGAGGTTAGGAGTTCGAGACCAGCCTGGCCTACATAGTGAGACCCCATCTCTACAAAATCACA T A EIF6 Ensembl:ENSG00000242372 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1411022421 Functional Loss SNV dbSNP153 33..33 33 - - - 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 49532 RMVar_ID_49532 Human_SNP_ID_679759695 A-to-I Human chr20 - 35283211 35283211 35283211 CACGATCTTGGCTCACTGCAACACTCTCTTCAAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGCT CACGATCTTGGCTCACTGCAACACTCTCTTCAGGTGATTCTCCTGCCTCAGCCTCCCAAGTAGCT T C EIF6 Ensembl:ENSG00000242372 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886356567 Functional Loss SNV dbSNP153 33..33 33 - - - 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 49533 RMVar_ID_49533 Human_SNP_ID_679767172 A-to-I Human chr20 - 35310940 35310940 35310940 TAATCCCAGCACTTTGGGAGGCCGAGGTGGATAGATCACGAGGCCAAGAGTTCGAGACCAGCCTG TAATCCCAGCACTTTGGGAGGCCGAGGTGGATGGATCACGAGGCCAAGAGTTCGAGACCAGCCTG T C UQCC1 Ensembl:ENSG00000101019 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1392158924 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25605287 49534 RMVar_ID_49534 Human_SNP_ID_679767657 A-to-I Human chr20 - 35313316 35313316 35313316 GCTGGAGTGCAGTGGCGCGATCTCTACTTACCACAAGCTCCACCTCCCAGGTTCACGCCATTCTT GCTGGAGTGCAGTGGCGCGATCTCTACTTACCGCAAGCTCCACCTCCCAGGTTCACGCCATTCTT T C UQCC1 Ensembl:ENSG00000101019 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1246980570 Functional Loss SNV dbSNP153 33..33 33 - - - 49535 RMVar_ID_49535 Human_SNP_ID_679767658 A-to-I Human chr20 - 35313316 35313316 35313316 GCTGGAGTGCAGTGGCGCGATCTCTACTTACCACAAGCTCCACCTCCCAGGTTCACGCCATTCTT GCTGGAGTGCAGTGGCGCGATCTCTACTTACCCCAAGCTCCACCTCCCAGGTTCACGCCATTCTT T G UQCC1 Ensembl:ENSG00000101019 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1246980570 Functional Loss SNV dbSNP153 33..33 33 - - - 49536 RMVar_ID_49536 Human_SNP_ID_679777538 A-to-I Human chr20 - 35358698 35358698 35358698 AAAATTGGCTGGGTGTGGTGGTGGGTGCCTGTAATCCCAGCTACTCAGGAAGCTGAGGCAGGAGA AAAATTGGCTGGGTGTGGTGGTGGGTGCCTGTGATCCCAGCTACTCAGGAAGCTGAGGCAGGAGA T C UQCC1 Ensembl:ENSG00000101019 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs928622021 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_44885,RMVar_hsa_circ_316254,RMVar_hsa_circ_344263,RMVar_hsa_circ_323431,RMVar_hsa_circ_281470,RMVar_hsa_circ_331871 49537 RMVar_ID_49537 Human_SNP_ID_679780601 A-to-I Human chr20 - 35372850 35372850 35372850 TGTTTTTTGAGACTTGCTTTGAGTCTTGCTCTATTGCCCAGATTGGAGTGGAGTGGTGCCATCTT TGTTTTTTGAGACTTGCTTTGAGTCTTGCTCTGTTGCCCAGATTGGAGTGGAGTGGTGCCATCTT T C UQCC1 Ensembl:ENSG00000101019 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs566437368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6994392,Human_RBP_ID_17571546,Human_RBP_ID_22817217 RMVar_hsa_circ_44885,RMVar_hsa_circ_316254,RMVar_hsa_circ_344263,RMVar_hsa_circ_323431,RMVar_hsa_circ_281470,RMVar_hsa_circ_331871,RMVar_hsa_circ_209686,RMVar_hsa_circ_111951,RMVar_hsa_circ_280783,RMVar_hsa_circ_284454,RMVar_hsa_circ_209682,RMVar_hsa_circ_281423,RMVar_hsa_circ_270410,RMVar_hsa_circ_26163,RMVar_hsa_circ_209687,RMVar_hsa_circ_209684,RMVar_hsa_circ_209685,RMVar_hsa_circ_209683 49538 RMVar_ID_49538 Human_SNP_ID_679789586 A-to-I Human chr20 - 35409841 35409841 35409841 AGATTGTGCCACTGCAGTCCAGCCTGGGTGAAAGAGTGAAACTCTGTCTGAAAAAAAAAAAGAAG AGATTGTGCCACTGCAGTCCAGCCTGGGTGAATGAGTGAAACTCTGTCTGAAAAAAAAAAAGAAG T A UQCC1 Ensembl:ENSG00000101019 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs751961909 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571548 RMVar_hsa_circ_96573,RMVar_hsa_circ_209693 49539 RMVar_ID_49539 Human_SNP_ID_679789654 A-to-I Human chr20 - 35410101 35410101 35410101 GAAAACTGAACCACAGAGAGGTATTCCTGGCCAGGTGCCGTGGCTCACACCTGTAATCCCAGCAC GAAAACTGAACCACAGAGAGGTATTCCTGGCCGGGTGCCGTGGCTCACACCTGTAATCCCAGCAC T C UQCC1 Ensembl:ENSG00000101019 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs997487015 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2076037 RMVar_hsa_circ_96573,RMVar_hsa_circ_209693 49540 RMVar_ID_49540 Human_SNP_ID_679800770 A-to-I Human chr20 - 35451674 35451674 35451674 AAAAAAATGAGGTGAGAGGATTGCTTGAGCCCAGGAGGTCGAGGCTGCAATGAGCCGTGATGGCC AAAAAAATGAGGTGAGAGGATTGCTTGAGCCCCGGAGGTCGAGGCTGCAATGAGCCGTGATGGCC T G GDF5 Ensembl:ENSG00000125965 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251350394 Functional Loss SNV dbSNP153 33..33 33 - - - 49541 RMVar_ID_49541 Human_SNP_ID_679808930 A-to-I Human chr20 + 35485539 35485539 35485539 AGAGATAAGGTCTTGCTCTGGTCACCCAGGCTAGAGTATAGTGGCACAATCATAGCTCACTGCAG AGAGATAAGGTCTTGCTCTGGTCACCCAGGCTGGAGTATAGTGGCACAATCATAGCTCACTGCAG A G CEP250 Ensembl:ENSG00000126001 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1287807857 Functional Loss SNV dbSNP153 33..33 33 - - - 49542 RMVar_ID_49542 Human_SNP_ID_679808931 A-to-I Human chr20 + 35485539 35485539 35485539 AGAGATAAGGTCTTGCTCTGGTCACCCAGGCTAGAGTATAGTGGCACAATCATAGCTCACTGCAG AGAGATAAGGTCTTGCTCTGGTCACCCAGGCTTGAGTATAGTGGCACAATCATAGCTCACTGCAG A T CEP250 Ensembl:ENSG00000126001 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1287807857 Functional Loss SNV dbSNP153 33..33 33 - - - 49543 RMVar_ID_49543 Human_SNP_ID_679816051 A-to-I Human chr20 + 35513358 35513358 35513358 CTCACCAGTGGCAACATCCACCTCCTGGGTTCAAGCAATTCTCCTGCCTCGGCCTCCTGTGTATC CTCACCAGTGGCAACATCCACCTCCTGGGTTCGAGCAATTCTCCTGCCTCGGCCTCCTGTGTATC A G CEP250 Ensembl:ENSG00000126001 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1456396340 Functional Loss SNV dbSNP153 33..33 33 - - - 49544 RMVar_ID_49544 Human_SNP_ID_679841876 A-to-I Human chr20 - 35608044 35608044 35608044 CAATTAGCCAGCTGTGGTGGTGGACACCTGTAATTCCAGCTACCCGGGAGGCTGAGACAGGAGAA CAATTAGCCAGCTGTGGTGGTGGACACCTGTAGTTCCAGCTACCCGGGAGGCTGAGACAGGAGAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1351145263 Functional Loss SNV dbSNP153 33..33 33 - - - 49545 RMVar_ID_49545 Human_SNP_ID_679846135 A-to-I Human chr20 - 35622407 35622403 35622407 TTATTTATTTATTTTATTTGAGATGGAGTCTCACTCTGTCGCCAGACTGGAGTGCAGTGGCACGA TTATTTATTTATTTTATTTGAGATGGAGTCTC____TGTCGCCAGACTGGAGTGCAGTGGCACGA AGAGT A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432571165 Functional Loss DEL dbSNP153 33..36 33 - - - 49546 RMVar_ID_49546 Human_SNP_ID_679847528 A-to-I Human chr20 - 35627389 35627389 35627389 CTCTGCAGGCATCCAGGGCATTGTGGATGCCTACCGCCAAGCCCTGCCCCAAGTTCGCCTCTATG CTCTGCAGGCATCCAGGGCATTGTGGATGCCTCCCGCCAAGCCCTGCCCCAAGTTCGCCTCTATG T G CPNE1 Ensembl:ENSG00000214078 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1441418354 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_63296,Human_RBP_ID_562659,Human_RBP_ID_923960,Human_RBP_ID_9348011,Human_RBP_ID_14085267,Human_RBP_ID_17512860,Human_RBP_ID_24560939,Human_RBP_ID_25606066,Human_RBP_ID_27484910 Human_Splice_Rec_2077114,Human_Splice_Rec_2077128,Human_Splice_Rec_2077158,Human_Splice_Rec_2077188,Human_Splice_Rec_2077216,Human_Splice_Rec_2077246,Human_Splice_Rec_2077268,Human_Splice_Rec_2077298,Human_Splice_Rec_2077328,Human_Splice_Rec_2077356 RMVar_hsa_circ_47999,RMVar_hsa_circ_109214,RMVar_hsa_circ_106269,RMVar_hsa_circ_116446,RMVar_hsa_circ_209720,RMVar_hsa_circ_69220,RMVar_hsa_circ_209721,RMVar_hsa_circ_21402,RMVar_hsa_circ_39545,RMVar_hsa_circ_209722 49547 RMVar_ID_49547 Human_SNP_ID_679848182 A-to-I Human chr20 - 35630035 35630035 35630035 CCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGTATTGAGCCACAGCGCCTGACCCAGAGGGT CCTGCCTTGGCCTCCCAAAGTGCTGGGATTACGGGTATTGAGCCACAGCGCCTGACCCAGAGGGT T C CPNE1 Ensembl:ENSG00000214078 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs895583277 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571560,Human_RBP_ID_22479118 RMVar_hsa_circ_47999,RMVar_hsa_circ_116446,RMVar_hsa_circ_69220,RMVar_hsa_circ_21402,RMVar_hsa_circ_39545,RMVar_hsa_circ_209722 49548 RMVar_ID_49548 Human_SNP_ID_679848216 A-to-I Human chr20 - 35630186 35630186 35630186 GGGTTCGAGCAATTCTTCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGTCGCTTGCCACCGTG GGGTTCGAGCAATTCTTCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGTCGCTTGCCACCGTG T C CPNE1 Ensembl:ENSG00000214078 Protein coding intron GSE38233;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,32596459 RNA-Seq:(High) rs1283036500 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47999,RMVar_hsa_circ_116446,RMVar_hsa_circ_69220,RMVar_hsa_circ_21402,RMVar_hsa_circ_39545,RMVar_hsa_circ_209722 49549 RMVar_ID_49549 Human_SNP_ID_679849697 A-to-I Human chr20 - 35634478 35634478 35634478 GCGATTCTCCTGCCTCAGCCTCCCAAAGTGCTAGGATTACAGGCGCCCACCACCATACCAGCTAA GCGATTCTCCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGCCCACCACCATACCAGCTAA T C AL109827.1,CPNE1 Ensembl:ENSG00000272897,Ensembl:ENSG00000214078 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1373862632 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47999,RMVar_hsa_circ_371126,RMVar_hsa_circ_374552,RMVar_hsa_circ_336427,RMVar_hsa_circ_209726,RMVar_hsa_circ_209727 49550 RMVar_ID_49550 Human_SNP_ID_679853204 A-to-I Human chr20 - 35647887 35647887 35647887 TAATTTTTTTTTTTTTTTTTTTCATTTTTAGTAGAGACGGGGTTTTGCCATGTTGGCCAGCATAG TAATTTTTTTTTTTTTTTTTTTCATTTTTAGTGGAGACGGGGTTTTGCCATGTTGGCCAGCATAG T C AL109827.1,CPNE1 Ensembl:ENSG00000272897,Ensembl:ENSG00000214078 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1343993343 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2682849,Human_RBP_ID_14086073 RMVar_hsa_circ_47999,RMVar_hsa_circ_371126,RMVar_hsa_circ_374552,RMVar_hsa_circ_336427,RMVar_hsa_circ_209726,RMVar_hsa_circ_209727 49551 RMVar_ID_49551 Human_SNP_ID_679860406 A-to-I Human chr20 - 35675777 35675777 35675777 AACCTCTACCACCTGGGTTCATCTCATGTCTCAGCCTCCTGAGTAGCTGGGATTACATGTGCCTG AACCTCTACCACCTGGGTTCATCTCATGTCTCTGCCTCCTGAGTAGCTGGGATTACATGTGCCTG T A NFS1 Ensembl:ENSG00000244005 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1461179568 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60187,RMVar_hsa_circ_352515 49552 RMVar_ID_49552 Human_SNP_ID_679860407 A-to-I Human chr20 - 35675777 35675777 35675777 AACCTCTACCACCTGGGTTCATCTCATGTCTCAGCCTCCTGAGTAGCTGGGATTACATGTGCCTG AACCTCTACCACCTGGGTTCATCTCATGTCTCGGCCTCCTGAGTAGCTGGGATTACATGTGCCTG T C NFS1 Ensembl:ENSG00000244005 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1461179568 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60187,RMVar_hsa_circ_352515 49553 RMVar_ID_49553 Human_SNP_ID_679860885 A-to-I Human chr20 - 35677489 35677489 35677489 GTTGCCCAGCCTGGAGTGGAGTGAGTGGCACGATCATAGCTCACTGCAGCCTCGACCTCCTAGGC GTTGCCCAGCCTGGAGTGGAGTGAGTGGCACGGTCATAGCTCACTGCAGCCTCGACCTCCTAGGC T C NFS1 Ensembl:ENSG00000244005 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1324281097 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60187,RMVar_hsa_circ_352515 49554 RMVar_ID_49554 Human_SNP_ID_679862141 A-to-I Human chr20 - 35682645 35682645 35682645 GGCTGGGGCTACAGGTGTGTGCCACCAGGCCCAGCTAATTTTTGTATTTTTAGTAGAGACAGGGT GGCTGGGGCTACAGGTGTGTGCCACCAGGCCCGGCTAATTTTTGTATTTTTAGTAGAGACAGGGT T C NFS1 Ensembl:ENSG00000244005 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984775490 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60187,RMVar_hsa_circ_56155,RMVar_hsa_circ_54298 49555 RMVar_ID_49555 Human_SNP_ID_679864612 A-to-I Human chr20 - 35691792 35691792 35691792 CCTGCCTGAGCCTCCCAAAGTGGAGGGATTACAGGCATGAGCCACTGCACCTGGCGTTCTTTTTT CCTGCCTGAGCCTCCCAAAGTGGAGGGATTACTGGCATGAGCCACTGCACCTGGCGTTCTTTTTT T A NFS1 Ensembl:ENSG00000244005 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1293549347 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125220,RMVar_hsa_circ_54298,RMVar_hsa_circ_209741,RMVar_hsa_circ_121528,RMVar_hsa_circ_209740 49556 RMVar_ID_49556 Human_SNP_ID_679864639 A-to-I Human chr20 - 35691886 35691886 35691886 GAGCCACCGCGCCTGGCCATTTTTGTATTTTTAGTAGAGATGGGGTTCCACCATGTTCGTCAGGC GAGCCACCGCGCCTGGCCATTTTTGTATTTTTGGTAGAGATGGGGTTCCACCATGTTCGTCAGGC T C NFS1 Ensembl:ENSG00000244005 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs567257427 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14087339 RMVar_hsa_circ_125220,RMVar_hsa_circ_54298,RMVar_hsa_circ_209741,RMVar_hsa_circ_121528,RMVar_hsa_circ_209740 49557 RMVar_ID_49557 Human_SNP_ID_679864640 A-to-I Human chr20 - 35691886 35691886 35691886 GAGCCACCGCGCCTGGCCATTTTTGTATTTTTAGTAGAGATGGGGTTCCACCATGTTCGTCAGGC GAGCCACCGCGCCTGGCCATTTTTGTATTTTTCGTAGAGATGGGGTTCCACCATGTTCGTCAGGC T G NFS1 Ensembl:ENSG00000244005 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs567257427 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14087339 RMVar_hsa_circ_125220,RMVar_hsa_circ_54298,RMVar_hsa_circ_209741,RMVar_hsa_circ_121528,RMVar_hsa_circ_209740 49558 RMVar_ID_49558 Human_SNP_ID_679865196 A-to-I Human chr20 - 35693840 35693840 35693840 CTCCTGCCTCAGCCTCCTGAGTAGGTAGGACTACAGGCTCCCACCACCACGCCTGGCTAATTTTT CTCCTGCCTCAGCCTCCTGAGTAGGTAGGACTGCAGGCTCCCACCACCACGCCTGGCTAATTTTT T C NFS1 Ensembl:ENSG00000244005 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1164457589 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14087377 RMVar_hsa_circ_125220,RMVar_hsa_circ_54298,RMVar_hsa_circ_209741,RMVar_hsa_circ_121528,RMVar_hsa_circ_209740 49559 RMVar_ID_49559 Human_SNP_ID_679865246 A-to-I Human chr20 - 35694059 35694059 35694059 TCACTGGAGCCTTGAACTCCTGGACTCAAGCAATCCTCTCATCTTAGCCTCCCAAGTAGCTAGGC TCACTGGAGCCTTGAACTCCTGGACTCAAGCAGTCCTCTCATCTTAGCCTCCCAAGTAGCTAGGC T C NFS1 Ensembl:ENSG00000244005 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1417350545 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14087378 RMVar_hsa_circ_125220,RMVar_hsa_circ_54298,RMVar_hsa_circ_209741,RMVar_hsa_circ_121528,RMVar_hsa_circ_209740 49560 RMVar_ID_49560 Human_SNP_ID_679870645 A-to-I Human chr20 - 35713227 35713227 35713227 CTCCCTTGGCCTCCCAGAGTGCTAGCTAAGTTACAGGCGTCAACCACCACACTCGGCCCTCCTTG CTCCCTTGGCCTCCCAGAGTGCTAGCTAAGTTCCAGGCGTCAACCACCACACTCGGCCCTCCTTG T G RBM39 Ensembl:ENSG00000131051 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1350892677 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_63044,Human_RBP_ID_6995684,Human_RBP_ID_10027406,Human_RBP_ID_14088124,Human_RBP_ID_23005698,Human_RBP_ID_25606845 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 49561 RMVar_ID_49561 Human_SNP_ID_679870646 A-to-I Human chr20 - 35713236 35713236 35713236 GTGAACCACCTCCCTTGGCCTCCCAGAGTGCTAGCTAAGTTACAGGCGTCAACCACCACACTCGG GTGAACCACCTCCCTTGGCCTCCCAGAGTGCTTGCTAAGTTACAGGCGTCAACCACCACACTCGG T A RBM39 Ensembl:ENSG00000131051 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1309562808 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10027406,Human_RBP_ID_14088124,Human_RBP_ID_17571570,Human_RBP_ID_23005698 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 49562 RMVar_ID_49562 Human_SNP_ID_679870660 A-to-I Human chr20 - 35713269 35713269 35713269 TTGCCCAGGTTGGTCTCGATCTCTGGGATTTAAGTGAACCACCTCCCTTGGCCTCCCAGAGTGCT TTGCCCAGGTTGGTCTCGATCTCTGGGATTTAGGTGAACCACCTCCCTTGGCCTCCCAGAGTGCT T C RBM39 Ensembl:ENSG00000131051 Protein coding intron GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831 HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line - 29129909,29796672,31158229,32596459 RNA-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 49563 RMVar_ID_49563 Human_SNP_ID_679870879 A-to-I Human chr20 - 35713770 35713770 35713770 ACCTCTGCCTCTTTGGCTGAAGCCATCCTCCCACCCTAATCTCTAAATAGCTGGGACTAACAGTT ACCTCTGCCTCTTTGGCTGAAGCCATCCTCCCTCCCTAATCTCTAAATAGCTGGGACTAACAGTT T A RBM39 Ensembl:ENSG00000131051 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 31158229,32596459 RNA-Seq:(High) rs927847512 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6995709,Human_RBP_ID_9390495,Human_RBP_ID_14088172,Human_RBP_ID_17970651,Human_RBP_ID_18534489,Human_RBP_ID_23001483,Human_RBP_ID_25629668 Human_Splice_Rec_2078310,Human_Splice_Rec_2078311,Human_Splice_Rec_2078322 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 49564 RMVar_ID_49564 Human_SNP_ID_679870880 A-to-I Human chr20 - 35713770 35713770 35713770 ACCTCTGCCTCTTTGGCTGAAGCCATCCTCCCACCCTAATCTCTAAATAGCTGGGACTAACAGTT ACCTCTGCCTCTTTGGCTGAAGCCATCCTCCCGCCCTAATCTCTAAATAGCTGGGACTAACAGTT T C RBM39 Ensembl:ENSG00000131051 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 31158229,32596459 RNA-Seq:(High) rs927847512 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6995709,Human_RBP_ID_9390495,Human_RBP_ID_14088172,Human_RBP_ID_17970651,Human_RBP_ID_18534489,Human_RBP_ID_23001483,Human_RBP_ID_25629668 Human_Splice_Rec_2078310,Human_Splice_Rec_2078311,Human_Splice_Rec_2078322 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 49565 RMVar_ID_49565 Human_SNP_ID_679871835 A-to-I Human chr20 - 35717168 35717168 35717168 TCAAGCAATTCTTCTGCTTCAGCATTCCAAGTAGCTGGGCGTACAGGCATGCGCCACCAAGCCCA TCAAGCAATTCTTCTGCTTCAGCATTCCAAGTGGCTGGGCGTACAGGCATGCGCCACCAAGCCCA T C RBM39 Ensembl:ENSG00000131051 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs552431720 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14088325 RMVar_hsa_circ_1702,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_59071,RMVar_hsa_circ_209755,RMVar_hsa_circ_209752,RMVar_hsa_circ_271190,RMVar_hsa_circ_355090,RMVar_hsa_circ_364251,RMVar_hsa_circ_61216,RMVar_hsa_circ_306398,RMVar_hsa_circ_351540,RMVar_hsa_circ_209754,RMVar_hsa_circ_356537,RMVar_hsa_circ_336453,RMVar_hsa_circ_274436,RMVar_hsa_circ_55088,RMVar_hsa_circ_14238,RMVar_hsa_circ_209759,RMVar_hsa_circ_331526,RMVar_hsa_circ_209756,RMVar_hsa_circ_209757,RMVar_hsa_circ_209758,RMVar_hsa_circ_346406,RMVar_hsa_circ_348457,RMVar_hsa_circ_209761,RMVar_hsa_circ_283226,RMVar_hsa_circ_209760 49566 RMVar_ID_49566 Human_SNP_ID_679871841 A-to-I Human chr20 - 35717193 35717193 35717193 TCATTGCAACCTCTGCCTCCCGGGTTCAAGCAATTCTTCTGCTTCAGCATTCCAAGTAGCTGGGC TCATTGCAACCTCTGCCTCCCGGGTTCAAGCAGTTCTTCTGCTTCAGCATTCCAAGTAGCTGGGC T C RBM39 Ensembl:ENSG00000131051 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1051783036 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1702,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_59071,RMVar_hsa_circ_209755,RMVar_hsa_circ_209752,RMVar_hsa_circ_271190,RMVar_hsa_circ_355090,RMVar_hsa_circ_364251,RMVar_hsa_circ_61216,RMVar_hsa_circ_306398,RMVar_hsa_circ_351540,RMVar_hsa_circ_209754,RMVar_hsa_circ_356537,RMVar_hsa_circ_336453,RMVar_hsa_circ_274436,RMVar_hsa_circ_55088,RMVar_hsa_circ_14238,RMVar_hsa_circ_209759,RMVar_hsa_circ_331526,RMVar_hsa_circ_209756,RMVar_hsa_circ_209757,RMVar_hsa_circ_209758,RMVar_hsa_circ_346406,RMVar_hsa_circ_348457,RMVar_hsa_circ_209761,RMVar_hsa_circ_283226,RMVar_hsa_circ_209760 49567 RMVar_ID_49567 Human_SNP_ID_679872059 A-to-I Human chr20 - 35717843 35717843 35717843 AAAAAAAAAAAAGTTCCTTTCTTGTTTGAGACAGAGTCTCCCTCTGTGACTGAGGCTGGAGTGCA AAAAAAAAAAAAGTTCCTTTCTTGTTTGAGACGGAGTCTCCCTCTGTGACTGAGGCTGGAGTGCA T C RBM39 Ensembl:ENSG00000131051 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs899657385 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571869 RMVar_hsa_circ_1702,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_59071,RMVar_hsa_circ_209755,RMVar_hsa_circ_209752,RMVar_hsa_circ_271190,RMVar_hsa_circ_355090,RMVar_hsa_circ_364251,RMVar_hsa_circ_61216,RMVar_hsa_circ_306398,RMVar_hsa_circ_351540,RMVar_hsa_circ_209754,RMVar_hsa_circ_356537,RMVar_hsa_circ_336453,RMVar_hsa_circ_274436,RMVar_hsa_circ_55088,RMVar_hsa_circ_14238,RMVar_hsa_circ_209759,RMVar_hsa_circ_331526,RMVar_hsa_circ_209756,RMVar_hsa_circ_209757,RMVar_hsa_circ_209758,RMVar_hsa_circ_346406,RMVar_hsa_circ_348457,RMVar_hsa_circ_209761,RMVar_hsa_circ_283226,RMVar_hsa_circ_209760 49568 RMVar_ID_49568 Human_SNP_ID_679872607 A-to-I Human chr20 - 35719349 35719349 35719349 GTACTCAACTCTCTTCCAAACAGCTGTAAGCTATTAAGAAATTGAGTATGGGCCAGGCACAGTGG GTACTCAACTCTCTTCCAAACAGCTGTAAGCTGTTAAGAAATTGAGTATGGGCCAGGCACAGTGG T C RBM39 Ensembl:ENSG00000131051 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1297794030 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14088438 RMVar_hsa_circ_1702,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_59071,RMVar_hsa_circ_209755,RMVar_hsa_circ_209752,RMVar_hsa_circ_271190,RMVar_hsa_circ_355090,RMVar_hsa_circ_364251,RMVar_hsa_circ_61216,RMVar_hsa_circ_306398,RMVar_hsa_circ_351540,RMVar_hsa_circ_209754,RMVar_hsa_circ_356537,RMVar_hsa_circ_336453,RMVar_hsa_circ_274436,RMVar_hsa_circ_55088,RMVar_hsa_circ_14238,RMVar_hsa_circ_209759,RMVar_hsa_circ_331526,RMVar_hsa_circ_209756,RMVar_hsa_circ_209757,RMVar_hsa_circ_209758,RMVar_hsa_circ_346406,RMVar_hsa_circ_348457,RMVar_hsa_circ_209761,RMVar_hsa_circ_283226,RMVar_hsa_circ_209760 49569 RMVar_ID_49569 Human_SNP_ID_679872653 A-to-I Human chr20 - 35719485 35719484 35719485 GTTGGTCAGGTTGGTCTCGAACTCTTGACCTCAGGTGATCTACCCGCCTCGGTGTCCCAAAGTGT GTTGGTCAGGTTGGTCTCGAACTCTTGACCTC_GGTGATCTACCCGCCTCGGTGTCCCAAAGTGT CT C RBM39 Ensembl:ENSG00000131051 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1268218744 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_23183950 RMVar_hsa_circ_1702,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_59071,RMVar_hsa_circ_209755,RMVar_hsa_circ_209752,RMVar_hsa_circ_271190,RMVar_hsa_circ_355090,RMVar_hsa_circ_364251,RMVar_hsa_circ_61216,RMVar_hsa_circ_306398,RMVar_hsa_circ_351540,RMVar_hsa_circ_209754,RMVar_hsa_circ_356537,RMVar_hsa_circ_336453,RMVar_hsa_circ_274436,RMVar_hsa_circ_55088,RMVar_hsa_circ_14238,RMVar_hsa_circ_209759,RMVar_hsa_circ_331526,RMVar_hsa_circ_209756,RMVar_hsa_circ_209757,RMVar_hsa_circ_209758,RMVar_hsa_circ_346406,RMVar_hsa_circ_348457,RMVar_hsa_circ_209761,RMVar_hsa_circ_283226,RMVar_hsa_circ_209760 49570 RMVar_ID_49570 Human_SNP_ID_679872782 A-to-I Human chr20 - 35719868 35719868 35719868 TGAGGCAGGAGAGTCACTTGAACCCGGGTGGCAGAGATTGCAGTGAGCCGAGATCACGCCTGGAT TGAGGCAGGAGAGTCACTTGAACCCGGGTGGCGGAGATTGCAGTGAGCCGAGATCACGCCTGGAT T C RBM39 Ensembl:ENSG00000131051 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1410378749 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14088453,Human_RBP_ID_17571573,Human_RBP_ID_23311671 RMVar_hsa_circ_1702,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_59071,RMVar_hsa_circ_209755,RMVar_hsa_circ_209752,RMVar_hsa_circ_271190,RMVar_hsa_circ_355090,RMVar_hsa_circ_364251,RMVar_hsa_circ_61216,RMVar_hsa_circ_306398,RMVar_hsa_circ_351540,RMVar_hsa_circ_209754,RMVar_hsa_circ_356537,RMVar_hsa_circ_336453,RMVar_hsa_circ_274436,RMVar_hsa_circ_55088,RMVar_hsa_circ_14238,RMVar_hsa_circ_209759,RMVar_hsa_circ_331526,RMVar_hsa_circ_209756,RMVar_hsa_circ_209757,RMVar_hsa_circ_209758,RMVar_hsa_circ_346406,RMVar_hsa_circ_348457,RMVar_hsa_circ_209761,RMVar_hsa_circ_283226,RMVar_hsa_circ_209760 49571 RMVar_ID_49571 Human_SNP_ID_679872798 A-to-I Human chr20 - 35719911 35719911 35719911 GGGTGTGGTGGCGCATCCCTCTAATCCCAGCTACTTAAGAGGCTGAGGCAGGAGAGTCACTTGAA GGGTGTGGTGGCGCATCCCTCTAATCCCAGCTGCTTAAGAGGCTGAGGCAGGAGAGTCACTTGAA T C RBM39 Ensembl:ENSG00000131051 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs902860630 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14088456,Human_RBP_ID_17571573 RMVar_hsa_circ_1702,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_59071,RMVar_hsa_circ_209755,RMVar_hsa_circ_209752,RMVar_hsa_circ_271190,RMVar_hsa_circ_355090,RMVar_hsa_circ_364251,RMVar_hsa_circ_61216,RMVar_hsa_circ_306398,RMVar_hsa_circ_351540,RMVar_hsa_circ_209754,RMVar_hsa_circ_356537,RMVar_hsa_circ_336453,RMVar_hsa_circ_274436,RMVar_hsa_circ_55088,RMVar_hsa_circ_14238,RMVar_hsa_circ_209759,RMVar_hsa_circ_331526,RMVar_hsa_circ_209756,RMVar_hsa_circ_209757,RMVar_hsa_circ_209758,RMVar_hsa_circ_346406,RMVar_hsa_circ_348457,RMVar_hsa_circ_209761,RMVar_hsa_circ_283226,RMVar_hsa_circ_209760 49572 RMVar_ID_49572 Human_SNP_ID_679873013 A-to-I Human chr20 - 35720659 35720659 35720659 TCAAGCGATTCTCTTGCTTTAGCCTTCCGAGTAGTTGGGTTTACAGGTGCCTGCCATCATGCTCG TCAAGCGATTCTCTTGCTTTAGCCTTCCGAGTGGTTGGGTTTACAGGTGCCTGCCATCATGCTCG T C RBM39 Ensembl:ENSG00000131051 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs551280664 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1702,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_59071,RMVar_hsa_circ_209755,RMVar_hsa_circ_209752,RMVar_hsa_circ_271190,RMVar_hsa_circ_355090,RMVar_hsa_circ_364251,RMVar_hsa_circ_61216,RMVar_hsa_circ_306398,RMVar_hsa_circ_351540,RMVar_hsa_circ_209754,RMVar_hsa_circ_356537,RMVar_hsa_circ_336453,RMVar_hsa_circ_274436,RMVar_hsa_circ_55088,RMVar_hsa_circ_14238,RMVar_hsa_circ_209759,RMVar_hsa_circ_331526,RMVar_hsa_circ_209756,RMVar_hsa_circ_209757,RMVar_hsa_circ_209758,RMVar_hsa_circ_346406,RMVar_hsa_circ_348457,RMVar_hsa_circ_209761,RMVar_hsa_circ_283226,RMVar_hsa_circ_209760,RMVar_hsa_circ_209762,RMVar_hsa_circ_94242 49573 RMVar_ID_49573 Human_SNP_ID_679873964 A-to-I Human chr20 - 35723501 35723501 35723501 CCAGGAGGCAGAGGTTGCAGTGAGGCAAGATCACGCCATTGCACTGCAGCCTGGGCGACAAGAAC CCAGGAGGCAGAGGTTGCAGTGAGGCAAGATCGCGCCATTGCACTGCAGCCTGGGCGACAAGAAC T C RBM39 Ensembl:ENSG00000131051 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1456184618 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10016567 RMVar_hsa_circ_1702,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_209750,RMVar_hsa_circ_209751,RMVar_hsa_circ_73210,RMVar_hsa_circ_370386,RMVar_hsa_circ_50280,RMVar_hsa_circ_59071,RMVar_hsa_circ_209755,RMVar_hsa_circ_209752,RMVar_hsa_circ_271190,RMVar_hsa_circ_355090,RMVar_hsa_circ_364251,RMVar_hsa_circ_61216,RMVar_hsa_circ_306398,RMVar_hsa_circ_209754,RMVar_hsa_circ_356537,RMVar_hsa_circ_336453,RMVar_hsa_circ_274436,RMVar_hsa_circ_55088,RMVar_hsa_circ_14238,RMVar_hsa_circ_209759,RMVar_hsa_circ_331526,RMVar_hsa_circ_209756,RMVar_hsa_circ_209757,RMVar_hsa_circ_209758,RMVar_hsa_circ_348457,RMVar_hsa_circ_209761,RMVar_hsa_circ_283226,RMVar_hsa_circ_209760,RMVar_hsa_circ_61575,RMVar_hsa_circ_209762,RMVar_hsa_circ_94242,RMVar_hsa_circ_288175,RMVar_hsa_circ_328158,RMVar_hsa_circ_279741,RMVar_hsa_circ_51446,RMVar_hsa_circ_209764,RMVar_hsa_circ_209765,RMVar_hsa_circ_209763 49574 RMVar_ID_49574 Human_SNP_ID_679874710 A-to-I Human chr20 - 35725775 35725775 35725775 CCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGCAGAATTGCTTGAACTCAGGGAGGCGGAGGT CCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCCGCAGAATTGCTTGAACTCAGGGAGGCGGAGGT T G RBM39 Ensembl:ENSG00000131051 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1026603933 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_149420 RMVar_hsa_circ_1702,RMVar_hsa_circ_24049,RMVar_hsa_circ_65494,RMVar_hsa_circ_73210,RMVar_hsa_circ_50280,RMVar_hsa_circ_59071,RMVar_hsa_circ_209755,RMVar_hsa_circ_355090,RMVar_hsa_circ_364251,RMVar_hsa_circ_61216,RMVar_hsa_circ_306398,RMVar_hsa_circ_356537,RMVar_hsa_circ_336453,RMVar_hsa_circ_55088,RMVar_hsa_circ_14238,RMVar_hsa_circ_331526,RMVar_hsa_circ_209756,RMVar_hsa_circ_209757,RMVar_hsa_circ_209761,RMVar_hsa_circ_209760,RMVar_hsa_circ_61575,RMVar_hsa_circ_288175,RMVar_hsa_circ_328158,RMVar_hsa_circ_51446,RMVar_hsa_circ_28578,RMVar_hsa_circ_209765,RMVar_hsa_circ_318097,RMVar_hsa_circ_321303,RMVar_hsa_circ_68527,RMVar_hsa_circ_209767,RMVar_hsa_circ_58838 49575 RMVar_ID_49575 Human_SNP_ID_679874886 A-to-I Human chr20 - 35726332 35726331 35726333 GATCAGGAGATCAAGACCATCCTGGCTAACACAGTGGAATCCCATGTCTACTAAAAATACAGAAA GATCAGGAGATCAAGACCATCCTGGCTAACA__GTGGAATCCCATGTCTACTAAAAATACAGAAA CTG C RBM39 Ensembl:ENSG00000131051 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs908679900 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_6995906 RMVar_hsa_circ_1702,RMVar_hsa_circ_24049,RMVar_hsa_circ_65494,RMVar_hsa_circ_73210,RMVar_hsa_circ_50280,RMVar_hsa_circ_59071,RMVar_hsa_circ_209755,RMVar_hsa_circ_355090,RMVar_hsa_circ_364251,RMVar_hsa_circ_61216,RMVar_hsa_circ_306398,RMVar_hsa_circ_356537,RMVar_hsa_circ_336453,RMVar_hsa_circ_55088,RMVar_hsa_circ_14238,RMVar_hsa_circ_331526,RMVar_hsa_circ_209756,RMVar_hsa_circ_209757,RMVar_hsa_circ_209761,RMVar_hsa_circ_209760,RMVar_hsa_circ_61575,RMVar_hsa_circ_288175,RMVar_hsa_circ_328158,RMVar_hsa_circ_51446,RMVar_hsa_circ_28578,RMVar_hsa_circ_209765,RMVar_hsa_circ_318097,RMVar_hsa_circ_321303,RMVar_hsa_circ_68527,RMVar_hsa_circ_209767,RMVar_hsa_circ_58838 49576 RMVar_ID_49576 Human_SNP_ID_679874923 A-to-I Human chr20 - 35726426 35726426 35726426 CCTTGTTTTAGAAAAATTACCCTTTTTGGGCCAGGCGTGGTGGCTGACGCCTACAATCCGAGTAC CCTTGTTTTAGAAAAATTACCCTTTTTGGGCCGGGCGTGGTGGCTGACGCCTACAATCCGAGTAC T C RBM39 Ensembl:ENSG00000131051 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs906722446 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_244496,Human_RBP_ID_779094,Human_RBP_ID_831838,Human_RBP_ID_6995907,Human_RBP_ID_14088763 RMVar_hsa_circ_1702,RMVar_hsa_circ_24049,RMVar_hsa_circ_65494,RMVar_hsa_circ_73210,RMVar_hsa_circ_50280,RMVar_hsa_circ_59071,RMVar_hsa_circ_209755,RMVar_hsa_circ_355090,RMVar_hsa_circ_364251,RMVar_hsa_circ_61216,RMVar_hsa_circ_306398,RMVar_hsa_circ_356537,RMVar_hsa_circ_336453,RMVar_hsa_circ_55088,RMVar_hsa_circ_14238,RMVar_hsa_circ_331526,RMVar_hsa_circ_209756,RMVar_hsa_circ_209757,RMVar_hsa_circ_209761,RMVar_hsa_circ_209760,RMVar_hsa_circ_61575,RMVar_hsa_circ_288175,RMVar_hsa_circ_328158,RMVar_hsa_circ_51446,RMVar_hsa_circ_28578,RMVar_hsa_circ_209765,RMVar_hsa_circ_318097,RMVar_hsa_circ_321303,RMVar_hsa_circ_68527,RMVar_hsa_circ_209767,RMVar_hsa_circ_58838 49577 RMVar_ID_49577 Human_SNP_ID_679875050 A-to-I Human chr20 - 35726893 35726893 35726893 TGAACCCGTGAGATGGAGGTTGTGATGAGCCAAGATCACACCACTGCACTCCAGCCTGGGTGACA TGAACCCGTGAGATGGAGGTTGTGATGAGCCAGGATCACACCACTGCACTCCAGCCTGGGTGACA T C RBM39 Ensembl:ENSG00000131051 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs544943622 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14088797,Human_RBP_ID_17571871 RMVar_hsa_circ_1702,RMVar_hsa_circ_24049,RMVar_hsa_circ_65494,RMVar_hsa_circ_73210,RMVar_hsa_circ_50280,RMVar_hsa_circ_59071,RMVar_hsa_circ_209755,RMVar_hsa_circ_355090,RMVar_hsa_circ_364251,RMVar_hsa_circ_61216,RMVar_hsa_circ_306398,RMVar_hsa_circ_356537,RMVar_hsa_circ_336453,RMVar_hsa_circ_55088,RMVar_hsa_circ_14238,RMVar_hsa_circ_331526,RMVar_hsa_circ_209756,RMVar_hsa_circ_209757,RMVar_hsa_circ_209761,RMVar_hsa_circ_209760,RMVar_hsa_circ_61575,RMVar_hsa_circ_288175,RMVar_hsa_circ_328158,RMVar_hsa_circ_51446,RMVar_hsa_circ_28578,RMVar_hsa_circ_209765,RMVar_hsa_circ_318097,RMVar_hsa_circ_321303,RMVar_hsa_circ_68527,RMVar_hsa_circ_209767,RMVar_hsa_circ_58838 49578 RMVar_ID_49578 Human_SNP_ID_679875091 A-to-I Human chr20 - 35726989 35726988 35726989 AACCCCATCTCTACTAATAAAGTACAAAAATTAGCCGGATGTAGTGGCGCGTGCGTGTAATCCCA AACCCCATCTCTACTAATAAAGTACAAAAATT_GCCGGATGTAGTGGCGCGTGCGTGTAATCCCA CT C RBM39 Ensembl:ENSG00000131051 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1467334605 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_6995918,Human_RBP_ID_8532001,Human_RBP_ID_14088800,Human_RBP_ID_17571583 RMVar_hsa_circ_1702,RMVar_hsa_circ_24049,RMVar_hsa_circ_65494,RMVar_hsa_circ_73210,RMVar_hsa_circ_50280,RMVar_hsa_circ_59071,RMVar_hsa_circ_209755,RMVar_hsa_circ_355090,RMVar_hsa_circ_364251,RMVar_hsa_circ_61216,RMVar_hsa_circ_306398,RMVar_hsa_circ_356537,RMVar_hsa_circ_336453,RMVar_hsa_circ_55088,RMVar_hsa_circ_14238,RMVar_hsa_circ_331526,RMVar_hsa_circ_209756,RMVar_hsa_circ_209757,RMVar_hsa_circ_209761,RMVar_hsa_circ_209760,RMVar_hsa_circ_61575,RMVar_hsa_circ_288175,RMVar_hsa_circ_328158,RMVar_hsa_circ_51446,RMVar_hsa_circ_28578,RMVar_hsa_circ_209765,RMVar_hsa_circ_318097,RMVar_hsa_circ_321303,RMVar_hsa_circ_68527,RMVar_hsa_circ_209767,RMVar_hsa_circ_58838 49579 RMVar_ID_49579 Human_SNP_ID_679875152 A-to-I Human chr20 - 35727173 35727173 35727173 GCTAATTTTTCTATTTTTTTTTTGTAGAGACAAGGTTTTGCCATGTTGCTCAGTTGGTCTGAAAA GCTAATTTTTCTATTTTTTTTTTGTAGAGACAGGGTTTTGCCATGTTGCTCAGTTGGTCTGAAAA T C RBM39 Ensembl:ENSG00000131051 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1423178248 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14088816,Human_RBP_ID_17571238 RMVar_hsa_circ_1702,RMVar_hsa_circ_24049,RMVar_hsa_circ_65494,RMVar_hsa_circ_73210,RMVar_hsa_circ_50280,RMVar_hsa_circ_59071,RMVar_hsa_circ_209755,RMVar_hsa_circ_355090,RMVar_hsa_circ_364251,RMVar_hsa_circ_61216,RMVar_hsa_circ_306398,RMVar_hsa_circ_356537,RMVar_hsa_circ_336453,RMVar_hsa_circ_55088,RMVar_hsa_circ_14238,RMVar_hsa_circ_331526,RMVar_hsa_circ_209756,RMVar_hsa_circ_209757,RMVar_hsa_circ_209761,RMVar_hsa_circ_209760,RMVar_hsa_circ_61575,RMVar_hsa_circ_288175,RMVar_hsa_circ_328158,RMVar_hsa_circ_51446,RMVar_hsa_circ_28578,RMVar_hsa_circ_209765,RMVar_hsa_circ_318097,RMVar_hsa_circ_321303,RMVar_hsa_circ_68527,RMVar_hsa_circ_209767,RMVar_hsa_circ_58838 49580 RMVar_ID_49580 Human_SNP_ID_679875172 A-to-I Human chr20 - 35727219 35727219 35727219 TTAGCCTCCCGAGTAGCTGGGACTATAGGTGCAGCCACCATGCCCTGCTAATTTTTCTATTTTTT TTAGCCTCCCGAGTAGCTGGGACTATAGGTGCGGCCACCATGCCCTGCTAATTTTTCTATTTTTT T C RBM39 Ensembl:ENSG00000131051 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1431088728 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571586 RMVar_hsa_circ_1702,RMVar_hsa_circ_24049,RMVar_hsa_circ_65494,RMVar_hsa_circ_73210,RMVar_hsa_circ_50280,RMVar_hsa_circ_59071,RMVar_hsa_circ_209755,RMVar_hsa_circ_355090,RMVar_hsa_circ_364251,RMVar_hsa_circ_61216,RMVar_hsa_circ_306398,RMVar_hsa_circ_356537,RMVar_hsa_circ_336453,RMVar_hsa_circ_55088,RMVar_hsa_circ_14238,RMVar_hsa_circ_331526,RMVar_hsa_circ_209756,RMVar_hsa_circ_209757,RMVar_hsa_circ_209761,RMVar_hsa_circ_209760,RMVar_hsa_circ_61575,RMVar_hsa_circ_288175,RMVar_hsa_circ_328158,RMVar_hsa_circ_51446,RMVar_hsa_circ_28578,RMVar_hsa_circ_209765,RMVar_hsa_circ_318097,RMVar_hsa_circ_321303,RMVar_hsa_circ_68527,RMVar_hsa_circ_209767,RMVar_hsa_circ_58838 49581 RMVar_ID_49581 Human_SNP_ID_679875474 A-to-I Human chr20 - 35728014 35728014 35728014 GGGAGACTGAGGTGGGTGGATCCACAAGGTCAAGAGATCGAGACCAGCCTGGCTAACATGGTGAA GGGAGACTGAGGTGGGTGGATCCACAAGGTCAGGAGATCGAGACCAGCCTGGCTAACATGGTGAA T C RBM39 Ensembl:ENSG00000131051 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1283050648 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1702,RMVar_hsa_circ_24049,RMVar_hsa_circ_65494,RMVar_hsa_circ_73210,RMVar_hsa_circ_50280,RMVar_hsa_circ_59071,RMVar_hsa_circ_209755,RMVar_hsa_circ_355090,RMVar_hsa_circ_364251,RMVar_hsa_circ_61216,RMVar_hsa_circ_306398,RMVar_hsa_circ_356537,RMVar_hsa_circ_336453,RMVar_hsa_circ_55088,RMVar_hsa_circ_14238,RMVar_hsa_circ_331526,RMVar_hsa_circ_209756,RMVar_hsa_circ_209757,RMVar_hsa_circ_209761,RMVar_hsa_circ_209760,RMVar_hsa_circ_61575,RMVar_hsa_circ_288175,RMVar_hsa_circ_328158,RMVar_hsa_circ_51446,RMVar_hsa_circ_28578,RMVar_hsa_circ_209765,RMVar_hsa_circ_318097,RMVar_hsa_circ_321303,RMVar_hsa_circ_68527,RMVar_hsa_circ_209767,RMVar_hsa_circ_58838 49582 RMVar_ID_49582 Human_SNP_ID_679875475 A-to-I Human chr20 - 35728014 35728014 35728014 GGGAGACTGAGGTGGGTGGATCCACAAGGTCAAGAGATCGAGACCAGCCTGGCTAACATGGTGAA GGGAGACTGAGGTGGGTGGATCCACAAGGTCACGAGATCGAGACCAGCCTGGCTAACATGGTGAA T G RBM39 Ensembl:ENSG00000131051 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1283050648 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1702,RMVar_hsa_circ_24049,RMVar_hsa_circ_65494,RMVar_hsa_circ_73210,RMVar_hsa_circ_50280,RMVar_hsa_circ_59071,RMVar_hsa_circ_209755,RMVar_hsa_circ_355090,RMVar_hsa_circ_364251,RMVar_hsa_circ_61216,RMVar_hsa_circ_306398,RMVar_hsa_circ_356537,RMVar_hsa_circ_336453,RMVar_hsa_circ_55088,RMVar_hsa_circ_14238,RMVar_hsa_circ_331526,RMVar_hsa_circ_209756,RMVar_hsa_circ_209757,RMVar_hsa_circ_209761,RMVar_hsa_circ_209760,RMVar_hsa_circ_61575,RMVar_hsa_circ_288175,RMVar_hsa_circ_328158,RMVar_hsa_circ_51446,RMVar_hsa_circ_28578,RMVar_hsa_circ_209765,RMVar_hsa_circ_318097,RMVar_hsa_circ_321303,RMVar_hsa_circ_68527,RMVar_hsa_circ_209767,RMVar_hsa_circ_58838 49583 RMVar_ID_49583 Human_SNP_ID_679875485 A-to-I Human chr20 - 35728059 35728059 35728059 TTGTAGGCCAGGCCCGGTGGCTCACGCGGGTAATCCCAGCACTTTGGGAGACTGAGGTGGGTGGA TTGTAGGCCAGGCCCGGTGGCTCACGCGGGTAGTCCCAGCACTTTGGGAGACTGAGGTGGGTGGA T C RBM39 Ensembl:ENSG00000131051 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1433963629 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6995936,Human_RBP_ID_14088866 RMVar_hsa_circ_1702,RMVar_hsa_circ_24049,RMVar_hsa_circ_65494,RMVar_hsa_circ_73210,RMVar_hsa_circ_50280,RMVar_hsa_circ_59071,RMVar_hsa_circ_209755,RMVar_hsa_circ_355090,RMVar_hsa_circ_364251,RMVar_hsa_circ_61216,RMVar_hsa_circ_306398,RMVar_hsa_circ_356537,RMVar_hsa_circ_336453,RMVar_hsa_circ_55088,RMVar_hsa_circ_14238,RMVar_hsa_circ_331526,RMVar_hsa_circ_209756,RMVar_hsa_circ_209757,RMVar_hsa_circ_209761,RMVar_hsa_circ_209760,RMVar_hsa_circ_61575,RMVar_hsa_circ_288175,RMVar_hsa_circ_328158,RMVar_hsa_circ_51446,RMVar_hsa_circ_28578,RMVar_hsa_circ_209765,RMVar_hsa_circ_318097,RMVar_hsa_circ_321303,RMVar_hsa_circ_68527,RMVar_hsa_circ_209767,RMVar_hsa_circ_58838 49584 RMVar_ID_49584 Human_SNP_ID_679875705 A-to-I Human chr20 - 35728834 35728834 35728834 ACCTCAGATGGTCCACCCACCTTGGCCTCTCAAAGTGGTAGGATTGCAGGTGTGAGCCAACACAC ACCTCAGATGGTCCACCCACCTTGGCCTCTCAGAGTGGTAGGATTGCAGGTGTGAGCCAACACAC T C RBM39 Ensembl:ENSG00000131051 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs925137263 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6995955,Human_RBP_ID_14088911 RMVar_hsa_circ_1702,RMVar_hsa_circ_24049,RMVar_hsa_circ_65494,RMVar_hsa_circ_73210,RMVar_hsa_circ_50280,RMVar_hsa_circ_59071,RMVar_hsa_circ_209755,RMVar_hsa_circ_355090,RMVar_hsa_circ_364251,RMVar_hsa_circ_61216,RMVar_hsa_circ_306398,RMVar_hsa_circ_356537,RMVar_hsa_circ_336453,RMVar_hsa_circ_55088,RMVar_hsa_circ_14238,RMVar_hsa_circ_331526,RMVar_hsa_circ_209756,RMVar_hsa_circ_209757,RMVar_hsa_circ_209761,RMVar_hsa_circ_209760,RMVar_hsa_circ_61575,RMVar_hsa_circ_288175,RMVar_hsa_circ_328158,RMVar_hsa_circ_51446,RMVar_hsa_circ_28578,RMVar_hsa_circ_209765,RMVar_hsa_circ_318097,RMVar_hsa_circ_321303,RMVar_hsa_circ_68527,RMVar_hsa_circ_209767,RMVar_hsa_circ_58838 49585 RMVar_ID_49585 Human_SNP_ID_679875718 A-to-I Human chr20 - 35728881 35728881 35728881 TAGCGATGGGATTTCACCATGTTGGCTAGCCTAGTGTTGAGCTCCGGACCTCAGATGGTCCACCC TAGCGATGGGATTTCACCATGTTGGCTAGCCTTGTGTTGAGCTCCGGACCTCAGATGGTCCACCC T A RBM39 Ensembl:ENSG00000131051 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992876763 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6995956,Human_RBP_ID_8532006,Human_RBP_ID_14088912,Human_RBP_ID_23001568 RMVar_hsa_circ_1702,RMVar_hsa_circ_24049,RMVar_hsa_circ_65494,RMVar_hsa_circ_73210,RMVar_hsa_circ_50280,RMVar_hsa_circ_59071,RMVar_hsa_circ_209755,RMVar_hsa_circ_355090,RMVar_hsa_circ_364251,RMVar_hsa_circ_61216,RMVar_hsa_circ_306398,RMVar_hsa_circ_356537,RMVar_hsa_circ_336453,RMVar_hsa_circ_55088,RMVar_hsa_circ_14238,RMVar_hsa_circ_331526,RMVar_hsa_circ_209756,RMVar_hsa_circ_209757,RMVar_hsa_circ_209761,RMVar_hsa_circ_209760,RMVar_hsa_circ_61575,RMVar_hsa_circ_288175,RMVar_hsa_circ_328158,RMVar_hsa_circ_51446,RMVar_hsa_circ_28578,RMVar_hsa_circ_209765,RMVar_hsa_circ_318097,RMVar_hsa_circ_321303,RMVar_hsa_circ_68527,RMVar_hsa_circ_209767,RMVar_hsa_circ_58838 49586 RMVar_ID_49586 Human_SNP_ID_679875728 A-to-I Human chr20 - 35728912 35728912 35728912 ACCACCATGCCTCGCTATTTTTTTATTTTAGTAGCGATGGGATTTCACCATGTTGGCTAGCCTAG ACCACCATGCCTCGCTATTTTTTTATTTTAGTTGCGATGGGATTTCACCATGTTGGCTAGCCTAG T A RBM39 Ensembl:ENSG00000131051 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1569051272 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6995959,Human_RBP_ID_14088921 RMVar_hsa_circ_1702,RMVar_hsa_circ_24049,RMVar_hsa_circ_65494,RMVar_hsa_circ_73210,RMVar_hsa_circ_50280,RMVar_hsa_circ_59071,RMVar_hsa_circ_209755,RMVar_hsa_circ_355090,RMVar_hsa_circ_364251,RMVar_hsa_circ_61216,RMVar_hsa_circ_306398,RMVar_hsa_circ_356537,RMVar_hsa_circ_336453,RMVar_hsa_circ_55088,RMVar_hsa_circ_14238,RMVar_hsa_circ_331526,RMVar_hsa_circ_209756,RMVar_hsa_circ_209757,RMVar_hsa_circ_209761,RMVar_hsa_circ_209760,RMVar_hsa_circ_61575,RMVar_hsa_circ_288175,RMVar_hsa_circ_328158,RMVar_hsa_circ_51446,RMVar_hsa_circ_28578,RMVar_hsa_circ_209765,RMVar_hsa_circ_318097,RMVar_hsa_circ_321303,RMVar_hsa_circ_68527,RMVar_hsa_circ_209767,RMVar_hsa_circ_58838 49587 RMVar_ID_49587 Human_SNP_ID_679875729 A-to-I Human chr20 - 35728915 35728915 35728915 TGCACCACCATGCCTCGCTATTTTTTTATTTTAGTAGCGATGGGATTTCACCATGTTGGCTAGCC TGCACCACCATGCCTCGCTATTTTTTTATTTTGGTAGCGATGGGATTTCACCATGTTGGCTAGCC T C RBM39 Ensembl:ENSG00000131051 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs948857800 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6995959,Human_RBP_ID_14088921 RMVar_hsa_circ_1702,RMVar_hsa_circ_24049,RMVar_hsa_circ_65494,RMVar_hsa_circ_73210,RMVar_hsa_circ_50280,RMVar_hsa_circ_59071,RMVar_hsa_circ_209755,RMVar_hsa_circ_355090,RMVar_hsa_circ_364251,RMVar_hsa_circ_61216,RMVar_hsa_circ_306398,RMVar_hsa_circ_356537,RMVar_hsa_circ_336453,RMVar_hsa_circ_55088,RMVar_hsa_circ_14238,RMVar_hsa_circ_331526,RMVar_hsa_circ_209756,RMVar_hsa_circ_209757,RMVar_hsa_circ_209761,RMVar_hsa_circ_209760,RMVar_hsa_circ_61575,RMVar_hsa_circ_288175,RMVar_hsa_circ_328158,RMVar_hsa_circ_51446,RMVar_hsa_circ_28578,RMVar_hsa_circ_209765,RMVar_hsa_circ_318097,RMVar_hsa_circ_321303,RMVar_hsa_circ_68527,RMVar_hsa_circ_209767,RMVar_hsa_circ_58838 49588 RMVar_ID_49588 Human_SNP_ID_679875746 A-to-I Human chr20 - 35728968 35728968 35728968 GGGTTCAAGCAGTTCTTCTACCTCAGCCCTCCAAGTAGCTGGGATTACAGGCATGCACCACCATG GGGTTCAAGCAGTTCTTCTACCTCAGCCCTCCGAGTAGCTGGGATTACAGGCATGCACCACCATG T C RBM39 Ensembl:ENSG00000131051 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1259479389 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1702,RMVar_hsa_circ_24049,RMVar_hsa_circ_65494,RMVar_hsa_circ_73210,RMVar_hsa_circ_50280,RMVar_hsa_circ_59071,RMVar_hsa_circ_209755,RMVar_hsa_circ_355090,RMVar_hsa_circ_364251,RMVar_hsa_circ_61216,RMVar_hsa_circ_306398,RMVar_hsa_circ_356537,RMVar_hsa_circ_336453,RMVar_hsa_circ_55088,RMVar_hsa_circ_14238,RMVar_hsa_circ_331526,RMVar_hsa_circ_209756,RMVar_hsa_circ_209757,RMVar_hsa_circ_209761,RMVar_hsa_circ_209760,RMVar_hsa_circ_61575,RMVar_hsa_circ_288175,RMVar_hsa_circ_328158,RMVar_hsa_circ_51446,RMVar_hsa_circ_28578,RMVar_hsa_circ_209765,RMVar_hsa_circ_318097,RMVar_hsa_circ_321303,RMVar_hsa_circ_68527,RMVar_hsa_circ_209767,RMVar_hsa_circ_58838 49589 RMVar_ID_49589 Human_SNP_ID_679876960 A-to-I Human chr20 - 35733216 35733216 35733216 TTGCTGCAACCTCCACCTCCCGGGTTCAAGCAATTCTCTTGCTTCAGCCTCCCAAGTAGCTGTGA TTGCTGCAACCTCCACCTCCCGGGTTCAAGCAGTTCTCTTGCTTCAGCCTCCCAAGTAGCTGTGA T C RBM39 Ensembl:ENSG00000131051 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6119646 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25607296 RMVar_hsa_circ_24049,RMVar_hsa_circ_73210,RMVar_hsa_circ_209755,RMVar_hsa_circ_355090,RMVar_hsa_circ_61216,RMVar_hsa_circ_356537,RMVar_hsa_circ_336453,RMVar_hsa_circ_55088,RMVar_hsa_circ_14238,RMVar_hsa_circ_21028,RMVar_hsa_circ_209756,RMVar_hsa_circ_61575,RMVar_hsa_circ_328158,RMVar_hsa_circ_51446,RMVar_hsa_circ_321303,RMVar_hsa_circ_209767,RMVar_hsa_circ_351966,RMVar_hsa_circ_355610,RMVar_hsa_circ_358112,RMVar_hsa_circ_366360,RMVar_hsa_circ_353222 49590 RMVar_ID_49590 Human_SNP_ID_679878072 A-to-I Human chr20 - 35736726 35736726 35736726 GAATCGCTTGAACCTGGGAGGCAGAGGTTGTAATGAGCTGAGATTATGCCATTGTACTCCAGCCT GAATCGCTTGAACCTGGGAGGCAGAGGTTGTAGTGAGCTGAGATTATGCCATTGTACTCCAGCCT T C RBM39 Ensembl:ENSG00000131051 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4519606 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22722927 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,RMVar_hsa_circ_209770 49591 RMVar_ID_49591 Human_SNP_ID_679878103 A-to-I Human chr20 - 35736817 35736817 35736817 GAAACCCCGTCTCTACTAAAAATACAAAAATTAGCTGGGCGTGGTGGTGCACGCCTGTAGTCCCA GAAACCCCGTCTCTACTAAAAATACAAAAATTGGCTGGGCGTGGTGGTGCACGCCTGTAGTCCCA T C RBM39 Ensembl:ENSG00000131051 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs919937174 Functional Loss SNV dbSNP153 33..33 33 - - - 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,RMVar_hsa_circ_209770 49592 RMVar_ID_49592 Human_SNP_ID_679878197 A-to-I Human chr20 - 35737074 35737074 35737074 TTTTGTGTTTTTAGTAGAGACAGGGTTTCACGATGTTGGCCAGGATGGTCTCCATCTCTTGACCT TTTTGTGTTTTTAGTAGAGACAGGGTTTCACGGTGTTGGCCAGGATGGTCTCCATCTCTTGACCT T C RBM39 Ensembl:ENSG00000131051 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1295471518 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14089496 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,RMVar_hsa_circ_209770 49593 RMVar_ID_49593 Human_SNP_ID_679878202 A-to-I Human chr20 - 35737085 35737083 35737085 GCCCAGCCAATTTTTGTGTTTTTAGTAGAGACAGGGTTTCACGATGTTGGCCAGGATGGTCTCCA GCCCAGCCAATTTTTGTGTTTTTAGTAGAGAC__GGTTTCACGATGTTGGCCAGGATGGTCTCCA CCT C RBM39 Ensembl:ENSG00000131051 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1251942735 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_14089496 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,RMVar_hsa_circ_209770 49594 RMVar_ID_49594 Human_SNP_ID_679878203 A-to-I Human chr20 - 35737085 35737085 35737085 GCCCAGCCAATTTTTGTGTTTTTAGTAGAGACAGGGTTTCACGATGTTGGCCAGGATGGTCTCCA GCCCAGCCAATTTTTGTGTTTTTAGTAGAGACGGGGTTTCACGATGTTGGCCAGGATGGTCTCCA T C RBM39 Ensembl:ENSG00000131051 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1388795397 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14089496 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,RMVar_hsa_circ_209770 49595 RMVar_ID_49595 Human_SNP_ID_679878336 A-to-I Human chr20 - 35737474 35737474 35737474 CTCACAGCAACCTCTGCCTCCTGGGTTCAGGCAGTTCTCCTGCCTCAGCCTCCCGAGTAGCTGGG CTCACAGCAACCTCTGCCTCCTGGGTTCAGGCTGTTCTCCTGCCTCAGCCTCCCGAGTAGCTGGG T A RBM39 Ensembl:ENSG00000131051 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs552816827 Functional Loss SNV dbSNP153 33..33 33 - - - 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,RMVar_hsa_circ_209770 49596 RMVar_ID_49596 Human_SNP_ID_679878337 A-to-I Human chr20 - 35737474 35737474 35737474 CTCACAGCAACCTCTGCCTCCTGGGTTCAGGCAGTTCTCCTGCCTCAGCCTCCCGAGTAGCTGGG CTCACAGCAACCTCTGCCTCCTGGGTTCAGGCGGTTCTCCTGCCTCAGCCTCCCGAGTAGCTGGG T C RBM39 Ensembl:ENSG00000131051 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs552816827 Functional Loss SNV dbSNP153 33..33 33 - - - 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,RMVar_hsa_circ_209770 49597 RMVar_ID_49597 Human_SNP_ID_679878401 A-to-I Human chr20 - 35737676 35737676 35737676 CCTGGCTAATTTTTTGTAATTTTAGTAGAGACAGGGTTTCATTGTGTTAGCCAGAATTGACCTTG CCTGGCTAATTTTTTGTAATTTTAGTAGAGACGGGGTTTCATTGTGTTAGCCAGAATTGACCTTG T C RBM39 Ensembl:ENSG00000131051 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs924706275 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14089521 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,RMVar_hsa_circ_209770 49598 RMVar_ID_49598 Human_SNP_ID_679878577 A-to-I Human chr20 - 35738035 35738035 35738035 TCCCCTGCCTCAGCCTCCGATTAGCTGGGACTACAGGCGCGCGCCATCACGCCTGGCTAATTTTT TCCCCTGCCTCAGCCTCCGATTAGCTGGGACTGCAGGCGCGCGCCATCACGCCTGGCTAATTTTT T C RBM39 Ensembl:ENSG00000131051 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256199729 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6996232,Human_RBP_ID_14089542 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,RMVar_hsa_circ_209770 49599 RMVar_ID_49599 Human_SNP_ID_679878657 A-to-I Human chr20 - 35738205 35738205 35738205 GGAGCGCAGTGGCGCAGTCTGGGCTCACTGCAACCTCCGCCTCCTGGGTTCAAGTGATTCTTTGA GGAGCGCAGTGGCGCAGTCTGGGCTCACTGCAGCCTCCGCCTCCTGGGTTCAAGTGATTCTTTGA T C RBM39 Ensembl:ENSG00000131051 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1239876323 Functional Loss SNV dbSNP153 33..33 33 - - - 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,RMVar_hsa_circ_209770 49600 RMVar_ID_49600 Human_SNP_ID_679889539 A-to-I Human chr20 + 35779084 35779084 35779084 TTGAGGTGGAGTCTCACTTCGTTGCCCAGGCTAGAGTACAATGGTGCAATCTCGGCTCACTGCAA TTGAGGTGGAGTCTCACTTCGTTGCCCAGGCTGGAGTACAATGGTGCAATCTCGGCTCACTGCAA A G PHF20 Ensembl:ENSG00000025293 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1191429526 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_209776,RMVar_hsa_circ_116170 49601 RMVar_ID_49601 Human_SNP_ID_679889899 A-to-I Human chr20 + 35780355 35780355 35780355 TTACGCCATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGATGCCCTCCACGATGCCCG TTACGCCATTCTCCTGCCTCAGCCTCCTGAGTTGCTGGGACTACAGATGCCCTCCACGATGCCCG A T PHF20 Ensembl:ENSG00000025293 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs956294949 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_209776,RMVar_hsa_circ_116170 49602 RMVar_ID_49602 Human_SNP_ID_679889916 A-to-I Human chr20 + 35780391 35780390 35780391 GGGACTACAGATGCCCTCCACGATGCCCGGCTAATTTTTTGTATTTTTAGTAGAGACAGGGGTTT GGGACTACAGATGCCCTCCACGATGCCCGGCT_ATTTTTTGTATTTTTAGTAGAGACAGGGGTTT TA T PHF20 Ensembl:ENSG00000025293 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1285195633 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_209776,RMVar_hsa_circ_116170 49603 RMVar_ID_49603 Human_SNP_ID_679889917 A-to-I Human chr20 + 35780391 35780391 35780391 GGGACTACAGATGCCCTCCACGATGCCCGGCTAATTTTTTGTATTTTTAGTAGAGACAGGGGTTT GGGACTACAGATGCCCTCCACGATGCCCGGCTTATTTTTTGTATTTTTAGTAGAGACAGGGGTTT A T PHF20 Ensembl:ENSG00000025293 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs964680469 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_209776,RMVar_hsa_circ_116170 49604 RMVar_ID_49604 Human_SNP_ID_679890499 A-to-I Human chr20 + 35782388 35782388 35782388 CTGACTGCAACCTCTGCCTCCTGGATTCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTAGG CTGACTGCAACCTCTGCCTCCTGGATTCAAGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTAGG A C PHF20 Ensembl:ENSG00000025293 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1003728416 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2078530,Human_Splice_Rec_2078538 RMVar_hsa_circ_209776,RMVar_hsa_circ_116170 49605 RMVar_ID_49605 Human_SNP_ID_679890520 A-to-I Human chr20 + 35782494 35782494 35782494 TTTGGAAGAGATGGGTTTTCACCATATTCGCCAAGCTAGTCTTGAACTCCTGACCTCAAGTGATC TTTGGAAGAGATGGGTTTTCACCATATTCGCCGAGCTAGTCTTGAACTCCTGACCTCAAGTGATC A G PHF20 Ensembl:ENSG00000025293 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs921868250 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_209776,RMVar_hsa_circ_116170 49606 RMVar_ID_49606 Human_SNP_ID_679890522 A-to-I Human chr20 + 35782499 35782499 35782499 AAGAGATGGGTTTTCACCATATTCGCCAAGCTAGTCTTGAACTCCTGACCTCAAGTGATCCACTC AAGAGATGGGTTTTCACCATATTCGCCAAGCTGGTCTTGAACTCCTGACCTCAAGTGATCCACTC A G PHF20 Ensembl:ENSG00000025293 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1331290206 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_209776,RMVar_hsa_circ_116170 49607 RMVar_ID_49607 Human_SNP_ID_679890533 A-to-I Human chr20 + 35782553 35782553 35782553 GTGATCCACTCTCCTCGGCCTCCCAAAGTGCTAGGATTACAGGCCACTGTGCCTGGCCAAGAGGT GTGATCCACTCTCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCCACTGTGCCTGGCCAAGAGGT A G PHF20 Ensembl:ENSG00000025293 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1036477194 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_2078531,Human_Splice_Rec_2078539 RMVar_hsa_circ_209776,RMVar_hsa_circ_116170 49608 RMVar_ID_49608 Human_SNP_ID_679890611 A-to-I Human chr20 + 35782944 35782944 35782944 GGCTGGGCACAGTGGCTCATGCCTGTAATCCCAGCACTCTGGGAGGCCAAGGCAGGAGGACTGCT GGCTGGGCACAGTGGCTCATGCCTGTAATCCCGGCACTCTGGGAGGCCAAGGCAGGAGGACTGCT A G PHF20 Ensembl:ENSG00000025293 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1229371760 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_209776,RMVar_hsa_circ_116170 49609 RMVar_ID_49609 Human_SNP_ID_679891047 A-to-I Human chr20 + 35784609 35784609 35784609 CAGGCGTGTGCCACTATGCCCAGCTAATTTTTATGTTGTTAACAGAGATGGAGTTTCACCATGTT CAGGCGTGTGCCACTATGCCCAGCTAATTTTTGTGTTGTTAACAGAGATGGAGTTTCACCATGTT A G PHF20 Ensembl:ENSG00000025293 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1159077087 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14178433 RMVar_hsa_circ_209776,RMVar_hsa_circ_116170 49610 RMVar_ID_49610 Human_SNP_ID_679892499 A-to-I Human chr20 + 35789680 35789680 35789680 GCAATTCTCCTGCCTTAGCCTCCTGAGTAGCTAGGACTACAGGCGTGCACCACCATGCCTGGCTA GCAATTCTCCTGCCTTAGCCTCCTGAGTAGCTGGGACTACAGGCGTGCACCACCATGCCTGGCTA A G PHF20 Ensembl:ENSG00000025293 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1231021411 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_209776,RMVar_hsa_circ_116170 49611 RMVar_ID_49611 Human_SNP_ID_679892662 A-to-I Human chr20 + 35790125 35790118 35790126 GTGATCCGCCCGCCTCTGCCTCCTAAAATGCTAGAATTACATGCATGAGCCACCATGCCCAGCAA GTGATCCGCCCGCCTCTGCCTCCTAA________AATTACATGCATGAGCCACCATGCCCAGCAA AAATGCTAG A PHF20 Ensembl:ENSG00000025293 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1380352824 Functional Loss DEL dbSNP153 27..34 33 - - - RMVar_hsa_circ_209776,RMVar_hsa_circ_116170 49612 RMVar_ID_49612 Human_SNP_ID_679892663 A-to-I Human chr20 + 35790125 35790125 35790125 GTGATCCGCCCGCCTCTGCCTCCTAAAATGCTAGAATTACATGCATGAGCCACCATGCCCAGCAA GTGATCCGCCCGCCTCTGCCTCCTAAAATGCTGGAATTACATGCATGAGCCACCATGCCCAGCAA A G PHF20 Ensembl:ENSG00000025293 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1242173202 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_209776,RMVar_hsa_circ_116170 49613 RMVar_ID_49613 Human_SNP_ID_679893678 A-to-I Human chr20 + 35793887 35793887 35793887 AGGCATGGTGGTGCACGCCTGTAATCCCAGCTACTGGGGAGGGTGAGGCAGGAGATGCTTGAACC AGGCATGGTGGTGCACGCCTGTAATCCCAGCTGCTGGGGAGGGTGAGGCAGGAGATGCTTGAACC A G PHF20 Ensembl:ENSG00000025293 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs961630524 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_209776,RMVar_hsa_circ_116170 49614 RMVar_ID_49614 Human_SNP_ID_679899893 A-to-I Human chr20 + 35817703 35817703 35817703 GGCTGTAGTCCCAGCTACTCAGGAGACAGGCTAGAGAATCCTTTGAGCCCGGGAAGCGGAGGTTG GGCTGTAGTCCCAGCTACTCAGGAGACAGGCTGGAGAATCCTTTGAGCCCGGGAAGCGGAGGTTG A G PHF20 Ensembl:ENSG00000025293 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1012363876 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14090309 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 49615 RMVar_ID_49615 Human_SNP_ID_679913175 A-to-I Human chr20 + 35874219 35874219 35874219 GCTGGTCTGGAACTCCTGACGTCAAGTGATCTACCCGCCTTGACTTCCCAAAGTACTGTGATTAT GCTGGTCTGGAACTCCTGACGTCAAGTGATCTCCCCGCCTTGACTTCCCAAAGTACTGTGATTAT A C PHF20 Ensembl:ENSG00000025293 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs980529041 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12929,RMVar_hsa_circ_70335,RMVar_hsa_circ_209776,RMVar_hsa_circ_116170,RMVar_hsa_circ_361489,RMVar_hsa_circ_369641,RMVar_hsa_circ_359144,RMVar_hsa_circ_280959,RMVar_hsa_circ_274402,RMVar_hsa_circ_105493,RMVar_hsa_circ_127931,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_209792,RMVar_hsa_circ_209793,RMVar_hsa_circ_108966,RMVar_hsa_circ_116796,RMVar_hsa_circ_86993,RMVar_hsa_circ_101281,RMVar_hsa_circ_209795,RMVar_hsa_circ_209796,RMVar_hsa_circ_293184,RMVar_hsa_circ_209794,RMVar_hsa_circ_288301,RMVar_hsa_circ_209803,RMVar_hsa_circ_357734,RMVar_hsa_circ_268774,RMVar_hsa_circ_63632,RMVar_hsa_circ_209806,RMVar_hsa_circ_50618,RMVar_hsa_circ_209808 49616 RMVar_ID_49616 Human_SNP_ID_679913176 A-to-I Human chr20 + 35874219 35874219 35874219 GCTGGTCTGGAACTCCTGACGTCAAGTGATCTACCCGCCTTGACTTCCCAAAGTACTGTGATTAT GCTGGTCTGGAACTCCTGACGTCAAGTGATCTGCCCGCCTTGACTTCCCAAAGTACTGTGATTAT A G PHF20 Ensembl:ENSG00000025293 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs980529041 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12929,RMVar_hsa_circ_70335,RMVar_hsa_circ_209776,RMVar_hsa_circ_116170,RMVar_hsa_circ_361489,RMVar_hsa_circ_369641,RMVar_hsa_circ_359144,RMVar_hsa_circ_280959,RMVar_hsa_circ_274402,RMVar_hsa_circ_105493,RMVar_hsa_circ_127931,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_209792,RMVar_hsa_circ_209793,RMVar_hsa_circ_108966,RMVar_hsa_circ_116796,RMVar_hsa_circ_86993,RMVar_hsa_circ_101281,RMVar_hsa_circ_209795,RMVar_hsa_circ_209796,RMVar_hsa_circ_293184,RMVar_hsa_circ_209794,RMVar_hsa_circ_288301,RMVar_hsa_circ_209803,RMVar_hsa_circ_357734,RMVar_hsa_circ_268774,RMVar_hsa_circ_63632,RMVar_hsa_circ_209806,RMVar_hsa_circ_50618,RMVar_hsa_circ_209808 49617 RMVar_ID_49617 Human_SNP_ID_679914712 A-to-I Human chr20 + 35880813 35880813 35880813 TGAAACCCTTTCTCTACAAAAATAAAAAAATTAGTCAGGCGTGATGGCACATGCTTGTAGTCCTA TGAAACCCTTTCTCTACAAAAATAAAAAAATTTGTCAGGCGTGATGGCACATGCTTGTAGTCCTA A T PHF20 Ensembl:ENSG00000025293 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1158670009 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12929,RMVar_hsa_circ_70335,RMVar_hsa_circ_209776,RMVar_hsa_circ_116170,RMVar_hsa_circ_361489,RMVar_hsa_circ_369641,RMVar_hsa_circ_359144,RMVar_hsa_circ_280959,RMVar_hsa_circ_274402,RMVar_hsa_circ_105493,RMVar_hsa_circ_127931,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_209792,RMVar_hsa_circ_209793,RMVar_hsa_circ_108966,RMVar_hsa_circ_116796,RMVar_hsa_circ_86993,RMVar_hsa_circ_101281,RMVar_hsa_circ_209795,RMVar_hsa_circ_209796,RMVar_hsa_circ_293184,RMVar_hsa_circ_209794,RMVar_hsa_circ_288301,RMVar_hsa_circ_209803,RMVar_hsa_circ_357734,RMVar_hsa_circ_268774,RMVar_hsa_circ_63632,RMVar_hsa_circ_209806,RMVar_hsa_circ_50618,RMVar_hsa_circ_209808 49618 RMVar_ID_49618 Human_SNP_ID_679915262 A-to-I Human chr20 + 35883093 35883093 35883093 ATAATTAGCTAGGCATTGTGGCACACGCCTGTAGTCCCAGCTACTCGGGAGGCTGACATGGGAGG ATAATTAGCTAGGCATTGTGGCACACGCCTGTTGTCCCAGCTACTCGGGAGGCTGACATGGGAGG A T PHF20 Ensembl:ENSG00000025293 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs986681685 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12929,RMVar_hsa_circ_70335,RMVar_hsa_circ_209776,RMVar_hsa_circ_116170,RMVar_hsa_circ_361489,RMVar_hsa_circ_369641,RMVar_hsa_circ_359144,RMVar_hsa_circ_280959,RMVar_hsa_circ_274402,RMVar_hsa_circ_105493,RMVar_hsa_circ_127931,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_209792,RMVar_hsa_circ_209793,RMVar_hsa_circ_108966,RMVar_hsa_circ_116796,RMVar_hsa_circ_86993,RMVar_hsa_circ_101281,RMVar_hsa_circ_209795,RMVar_hsa_circ_209796,RMVar_hsa_circ_293184,RMVar_hsa_circ_209794,RMVar_hsa_circ_288301,RMVar_hsa_circ_209803,RMVar_hsa_circ_357734,RMVar_hsa_circ_268774,RMVar_hsa_circ_63632,RMVar_hsa_circ_209806,RMVar_hsa_circ_50618,RMVar_hsa_circ_209808 49619 RMVar_ID_49619 Human_SNP_ID_679926507 A-to-I Human chr20 + 35932107 35932107 35932107 TTTTTTTTTTTGAGATGGAGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGTGAGATCATGGC TTTTTTTTTTTGAGATGGAGTCTCACTCTGTCCCCCAGGCTGGAGTGCAGTGGTGAGATCATGGC A C PHF20 Ensembl:ENSG00000025293 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027797561 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_359144,RMVar_hsa_circ_63632,RMVar_hsa_circ_305068,RMVar_hsa_circ_269427,RMVar_hsa_circ_364403,RMVar_hsa_circ_103653,RMVar_hsa_circ_360449,RMVar_hsa_circ_209816 49620 RMVar_ID_49620 Human_SNP_ID_679926508 A-to-I Human chr20 + 35932107 35932107 35932107 TTTTTTTTTTTGAGATGGAGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGTGAGATCATGGC TTTTTTTTTTTGAGATGGAGTCTCACTCTGTCGCCCAGGCTGGAGTGCAGTGGTGAGATCATGGC A G PHF20 Ensembl:ENSG00000025293 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027797561 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_359144,RMVar_hsa_circ_63632,RMVar_hsa_circ_305068,RMVar_hsa_circ_269427,RMVar_hsa_circ_364403,RMVar_hsa_circ_103653,RMVar_hsa_circ_360449,RMVar_hsa_circ_209816 49621 RMVar_ID_49621 Human_SNP_ID_679954127 A-to-I Human chr20 - 36047289 36047289 36047289 TAGGTGTTTAAAAGTGTACAACGGCCTGTCGCAGTGGCGCATGCCTGTAATCCCAGCACTTTGGG TAGGTGTTTAAAAGTGTACAACGGCCTGTCGCGGTGGCGCATGCCTGTAATCCCAGCACTTTGGG T C NORAD Ensembl:ENSG00000260032 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1262291609 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_563017,Human_RBP_ID_1929093,Human_RBP_ID_5100536,Human_RBP_ID_5148385,Human_RBP_ID_5201702,Human_RBP_ID_6996712,Human_RBP_ID_8205600,Human_RBP_ID_8854289,Human_RBP_ID_9116752,Human_RBP_ID_14091121,Human_RBP_ID_17192776,Human_RBP_ID_17282760,Human_RBP_ID_17511349,Human_RBP_ID_17970812,Human_RBP_ID_18322028,Human_RBP_ID_20648682,Human_RBP_ID_21895349,Human_RBP_ID_22395512,Human_RBP_ID_22452754 49622 RMVar_ID_49622 Human_SNP_ID_679968366 A-to-I Human chr20 + 36108260 36108260 36108260 CCTCAGCCTCCCAAAGTGTGGGGATTACAGGCATGAACCACCGTGCTGGGCCTATAGTATTTTTT CCTCAGCCTCCCAAAGTGTGGGGATTACAGGCGTGAACCACCGTGCTGGGCCTATAGTATTTTTT A G EPB41L1 Ensembl:ENSG00000088367 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs965939660 Functional Loss SNV dbSNP153 33..33 33 - - - 49623 RMVar_ID_49623 Human_SNP_ID_679999812 A-to-I Human chr20 + 36247684 36247684 36247684 GAGGTCAGGAGTTAGAGACCAGCCTGGCCAACATGGTGAAACCCCCATGTCTACTAAAAATACAA GAGGTCAGGAGTTAGAGACCAGCCTGGCCAACGTGGTGAAACCCCCATGTCTACTAAAAATACAA A G AAR2 Ensembl:ENSG00000131043 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1165747659 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108094,RMVar_hsa_circ_115622,RMVar_hsa_circ_209839,RMVar_hsa_circ_98688,RMVar_hsa_circ_209840,RMVar_hsa_circ_209841,RMVar_hsa_circ_116508,RMVar_hsa_circ_209845 49624 RMVar_ID_49624 Human_SNP_ID_680072038 A-to-I Human chr20 + 36545242 36545242 36545242 AAACTGGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGCGG AAACTGGGCCGGGCGCGGTGGCTCACGCCTGTGATCCCAGCACTTTGGGAGGCCAAGGCGGGCGG A G MYL9 Ensembl:ENSG00000101335 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs942326615 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78663,RMVar_hsa_circ_113653,RMVar_hsa_circ_209859,RMVar_hsa_circ_209860 49625 RMVar_ID_49625 Human_SNP_ID_680072094 A-to-I Human chr20 + 36545350 36545350 36545350 AAACCCTGACTCTACTAAAAATACCAAAAATTAGCCGAGCGTGGTGGCGGGCGCCTGTAGTCCCA AAACCCTGACTCTACTAAAAATACCAAAAATTGGCCGAGCGTGGTGGCGGGCGCCTGTAGTCCCA A G MYL9 Ensembl:ENSG00000101335 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1228437962 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78663,RMVar_hsa_circ_113653,RMVar_hsa_circ_209859,RMVar_hsa_circ_209860 49626 RMVar_ID_49626 Human_SNP_ID_680072115 A-to-I Human chr20 + 36545376 36545376 36545376 AAAATTAGCCGAGCGTGGTGGCGGGCGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA AAAATTAGCCGAGCGTGGTGGCGGGCGCCTGTGGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA A G MYL9 Ensembl:ENSG00000101335 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1306490050 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78663,RMVar_hsa_circ_113653,RMVar_hsa_circ_209859,RMVar_hsa_circ_209860 49627 RMVar_ID_49627 Human_SNP_ID_680072118 A-to-I Human chr20 + 36545386 36545386 36545386 GAGCGTGGTGGCGGGCGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATGGCGTGAA GAGCGTGGTGGCGGGCGCCTGTAGTCCCAGCTGCTTGGGAGGCTGAGGCAGGAGAATGGCGTGAA A G MYL9 Ensembl:ENSG00000101335 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1229905273 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78663,RMVar_hsa_circ_113653,RMVar_hsa_circ_209859,RMVar_hsa_circ_209860 49628 RMVar_ID_49628 Human_SNP_ID_680072290 A-to-I Human chr20 + 36545782 36545782 36545782 GAAACCCCGTCTCTACTAAAAATACAAAAATTAGCTGGGCGTGGTGGCGGGCGCCAGCTACTCGG GAAACCCCGTCTCTACTAAAAATACAAAAATTGGCTGGGCGTGGTGGCGGGCGCCAGCTACTCGG A G MYL9 Ensembl:ENSG00000101335 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388387114 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78663,RMVar_hsa_circ_113653,RMVar_hsa_circ_209859,RMVar_hsa_circ_209860 49629 RMVar_ID_49629 Human_SNP_ID_680072522 A-to-I Human chr20 + 36546638 36546638 36546638 ACTCCAGGGTTCTTTTTTTTTCCCCCCGAGACAAAATCTCACTCTGTTGCCCAGGCTGGAGTGGC ACTCCAGGGTTCTTTTTTTTTCCCCCCGAGACGAAATCTCACTCTGTTGCCCAGGCTGGAGTGGC A G MYL9 Ensembl:ENSG00000101335 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs950029851 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78663,RMVar_hsa_circ_113653,RMVar_hsa_circ_209859,RMVar_hsa_circ_209860 49630 RMVar_ID_49630 Human_SNP_ID_680072523 A-to-I Human chr20 + 36546639 36546639 36546639 CTCCAGGGTTCTTTTTTTTTCCCCCCGAGACAAAATCTCACTCTGTTGCCCAGGCTGGAGTGGCA CTCCAGGGTTCTTTTTTTTTCCCCCCGAGACAGAATCTCACTCTGTTGCCCAGGCTGGAGTGGCA A G MYL9 Ensembl:ENSG00000101335 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1046104850 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78663,RMVar_hsa_circ_113653,RMVar_hsa_circ_209859,RMVar_hsa_circ_209860 49631 RMVar_ID_49631 Human_SNP_ID_680072546 A-to-I Human chr20 + 36546749 36546749 36546749 CTCCTGCCTCAGCCTCCCCAGTAGCTGGGATTACAGACGTGCGCCACCATGCCCGGCTAATTTTT CTCCTGCCTCAGCCTCCCCAGTAGCTGGGATTGCAGACGTGCGCCACCATGCCCGGCTAATTTTT A G MYL9 Ensembl:ENSG00000101335 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1247120501 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78663,RMVar_hsa_circ_113653,RMVar_hsa_circ_209859,RMVar_hsa_circ_209860 49632 RMVar_ID_49632 Human_SNP_ID_680072575 A-to-I Human chr20 + 36546871 36546871 36546871 AGCCCATCTTGGCCTCCCAAAGTACTGGGATTACAGGTGTGAGCTACCACGCCTGGCCAACTCCA AGCCCATCTTGGCCTCCCAAAGTACTGGGATTGCAGGTGTGAGCTACCACGCCTGGCCAACTCCA A G MYL9 Ensembl:ENSG00000101335 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs915833655 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78663,RMVar_hsa_circ_113653,RMVar_hsa_circ_209859,RMVar_hsa_circ_209860 49633 RMVar_ID_49633 Human_SNP_ID_680072673 A-to-I Human chr20 + 36547360 36547360 36547360 AACAAGGAAACTGAGGCTCAGAGAGGTTAAGTAATTTACCCAAGGTCACACAGCTACCAAGTAGT AACAAGGAAACTGAGGCTCAGAGAGGTTAAGTGATTTACCCAAGGTCACACAGCTACCAAGTAGT A G MYL9 Ensembl:ENSG00000101335 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs932702731 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78663,RMVar_hsa_circ_113653,RMVar_hsa_circ_209859,RMVar_hsa_circ_209860 49634 RMVar_ID_49634 Human_SNP_ID_680072675 A-to-I Human chr20 + 36547365 36547365 36547365 GGAAACTGAGGCTCAGAGAGGTTAAGTAATTTACCCAAGGTCACACAGCTACCAAGTAGTGGGGC GGAAACTGAGGCTCAGAGAGGTTAAGTAATTTGCCCAAGGTCACACAGCTACCAAGTAGTGGGGC A G MYL9 Ensembl:ENSG00000101335 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049905208 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78663,RMVar_hsa_circ_113653,RMVar_hsa_circ_209859,RMVar_hsa_circ_209860 49635 RMVar_ID_49635 Human_SNP_ID_680081386 A-to-I Human chr20 + 36581006 36581006 36581006 AAAAATTGCCAGGTGTGGTGGTGCATGCCTGTAATCCAAGCTACTCGGGAGGCTGAGGCAGGAGA AAAAATTGCCAGGTGTGGTGGTGCATGCCTGTGATCCAAGCTACTCGGGAGGCTGAGGCAGGAGA A G TGIF2,TGIF2-RAB5IF Ensembl:ENSG00000118707,Ensembl:ENSG00000259399 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1325672350 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106038,RMVar_hsa_circ_117136,RMVar_hsa_circ_209863,RMVar_hsa_circ_87911,RMVar_hsa_circ_209865,RMVar_hsa_circ_209866 49636 RMVar_ID_49636 Human_SNP_ID_680081612 A-to-I Human chr20 + 36582016 36582016 36582016 CCAATACTTTGCGAGGCCGATGCGGGCGGATCACCTGAGGTCAGGAGTTCAAGACCAGCCTGACC CCAATACTTTGCGAGGCCGATGCGGGCGGATCGCCTGAGGTCAGGAGTTCAAGACCAGCCTGACC A G TGIF2,TGIF2-RAB5IF Ensembl:ENSG00000118707,Ensembl:ENSG00000259399 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs909498464 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106038,RMVar_hsa_circ_117136,RMVar_hsa_circ_209863,RMVar_hsa_circ_87911,RMVar_hsa_circ_209865,RMVar_hsa_circ_209866 49637 RMVar_ID_49637 Human_SNP_ID_680081613 A-to-I Human chr20 + 36582016 36582016 36582016 CCAATACTTTGCGAGGCCGATGCGGGCGGATCACCTGAGGTCAGGAGTTCAAGACCAGCCTGACC CCAATACTTTGCGAGGCCGATGCGGGCGGATCTCCTGAGGTCAGGAGTTCAAGACCAGCCTGACC A T TGIF2,TGIF2-RAB5IF Ensembl:ENSG00000118707,Ensembl:ENSG00000259399 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs909498464 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106038,RMVar_hsa_circ_117136,RMVar_hsa_circ_209863,RMVar_hsa_circ_87911,RMVar_hsa_circ_209865,RMVar_hsa_circ_209866 49638 RMVar_ID_49638 Human_SNP_ID_680081627 A-to-I Human chr20 + 36582034 36582034 36582034 GATGCGGGCGGATCACCTGAGGTCAGGAGTTCAAGACCAGCCTGACCAACATGGTGAAACCCCAT GATGCGGGCGGATCACCTGAGGTCAGGAGTTCGAGACCAGCCTGACCAACATGGTGAAACCCCAT A G TGIF2,TGIF2-RAB5IF Ensembl:ENSG00000118707,Ensembl:ENSG00000259399 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs180886427 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571599 RMVar_hsa_circ_106038,RMVar_hsa_circ_117136,RMVar_hsa_circ_209863,RMVar_hsa_circ_87911,RMVar_hsa_circ_209865,RMVar_hsa_circ_209866 49639 RMVar_ID_49639 Human_SNP_ID_680081630 A-to-I Human chr20 + 36582049 36582049 36582049 CCTGAGGTCAGGAGTTCAAGACCAGCCTGACCAACATGGTGAAACCCCATCTCTCCTAAAAATAC CCTGAGGTCAGGAGTTCAAGACCAGCCTGACCCACATGGTGAAACCCCATCTCTCCTAAAAATAC A C TGIF2,TGIF2-RAB5IF Ensembl:ENSG00000118707,Ensembl:ENSG00000259399 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1274715357 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571599 RMVar_hsa_circ_106038,RMVar_hsa_circ_117136,RMVar_hsa_circ_209863,RMVar_hsa_circ_87911,RMVar_hsa_circ_209865,RMVar_hsa_circ_209866 49640 RMVar_ID_49640 Human_SNP_ID_680082123 A-to-I Human chr20 + 36583999 36583999 36583999 TGAGGCAAGAGAATTGCTTGAACTCGGGAGGCAGAGGTTGTAGTGAGTTGTGATTGCACCATTGC TGAGGCAAGAGAATTGCTTGAACTCGGGAGGCGGAGGTTGTAGTGAGTTGTGATTGCACCATTGC A G TGIF2,TGIF2-RAB5IF Ensembl:ENSG00000118707,Ensembl:ENSG00000259399 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs529476 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106038,RMVar_hsa_circ_117136,RMVar_hsa_circ_209863,RMVar_hsa_circ_87911,RMVar_hsa_circ_209865,RMVar_hsa_circ_209866 49641 RMVar_ID_49641 Human_SNP_ID_680082124 A-to-I Human chr20 + 36583999 36583999 36583999 TGAGGCAAGAGAATTGCTTGAACTCGGGAGGCAGAGGTTGTAGTGAGTTGTGATTGCACCATTGC TGAGGCAAGAGAATTGCTTGAACTCGGGAGGCTGAGGTTGTAGTGAGTTGTGATTGCACCATTGC A T TGIF2,TGIF2-RAB5IF Ensembl:ENSG00000118707,Ensembl:ENSG00000259399 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs529476 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106038,RMVar_hsa_circ_117136,RMVar_hsa_circ_209863,RMVar_hsa_circ_87911,RMVar_hsa_circ_209865,RMVar_hsa_circ_209866 49642 RMVar_ID_49642 Human_SNP_ID_680082304 A-to-I Human chr20 + 36584640 36584640 36584640 GCAATCTCAGTTCACTGCAACTTCTGCTGCCCAGGTTCAAGCAATTCTCCTGCCCCAGCCTCCCG GCAATCTCAGTTCACTGCAACTTCTGCTGCCCGGGTTCAAGCAATTCTCCTGCCCCAGCCTCCCG A G TGIF2,TGIF2-RAB5IF Ensembl:ENSG00000118707,Ensembl:ENSG00000259399 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1022460560 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106038,RMVar_hsa_circ_117136,RMVar_hsa_circ_209863,RMVar_hsa_circ_87911,RMVar_hsa_circ_209865,RMVar_hsa_circ_209866 49643 RMVar_ID_49643 Human_SNP_ID_680082321 A-to-I Human chr20 + 36584727 36584727 36584727 TGCCACCAGGCTGAGCTAATTTTTGTAGTTTTAGTAAAGACAGGGTTTCACCATTTTGGCCAGGC TGCCACCAGGCTGAGCTAATTTTTGTAGTTTTGGTAAAGACAGGGTTTCACCATTTTGGCCAGGC A G TGIF2,TGIF2-RAB5IF Ensembl:ENSG00000118707,Ensembl:ENSG00000259399 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1325366541 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106038,RMVar_hsa_circ_117136,RMVar_hsa_circ_209863,RMVar_hsa_circ_87911,RMVar_hsa_circ_209865,RMVar_hsa_circ_209866 49644 RMVar_ID_49644 Human_SNP_ID_680082322 A-to-I Human chr20 + 36584730 36584730 36584730 CACCAGGCTGAGCTAATTTTTGTAGTTTTAGTAAAGACAGGGTTTCACCATTTTGGCCAGGCTGG CACCAGGCTGAGCTAATTTTTGTAGTTTTAGTGAAGACAGGGTTTCACCATTTTGGCCAGGCTGG A G TGIF2,TGIF2-RAB5IF Ensembl:ENSG00000118707,Ensembl:ENSG00000259399 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs967825245 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106038,RMVar_hsa_circ_117136,RMVar_hsa_circ_209863,RMVar_hsa_circ_87911,RMVar_hsa_circ_209865,RMVar_hsa_circ_209866 49645 RMVar_ID_49645 Human_SNP_ID_680082323 A-to-I Human chr20 + 36584736 36584735 36584737 GCTGAGCTAATTTTTGTAGTTTTAGTAAAGACAGGGTTTCACCATTTTGGCCAGGCTGGTCTCGA GCTGAGCTAATTTTTGTAGTTTTAGTAAAGAC__GGTTTCACCATTTTGGCCAGGCTGGTCTCGA CAG C TGIF2,TGIF2-RAB5IF Ensembl:ENSG00000118707,Ensembl:ENSG00000259399 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1022314018 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_106038,RMVar_hsa_circ_117136,RMVar_hsa_circ_209863,RMVar_hsa_circ_87911,RMVar_hsa_circ_209865,RMVar_hsa_circ_209866 49646 RMVar_ID_49646 Human_SNP_ID_680082325 A-to-I Human chr20 + 36584736 36584736 36584736 GCTGAGCTAATTTTTGTAGTTTTAGTAAAGACAGGGTTTCACCATTTTGGCCAGGCTGGTCTCGA GCTGAGCTAATTTTTGTAGTTTTAGTAAAGACGGGGTTTCACCATTTTGGCCAGGCTGGTCTCGA A G TGIF2,TGIF2-RAB5IF Ensembl:ENSG00000118707,Ensembl:ENSG00000259399 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs996607514 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106038,RMVar_hsa_circ_117136,RMVar_hsa_circ_209863,RMVar_hsa_circ_87911,RMVar_hsa_circ_209865,RMVar_hsa_circ_209866 49647 RMVar_ID_49647 Human_SNP_ID_680082331 A-to-I Human chr20 + 36584747 36584747 36584747 TTTTGTAGTTTTAGTAAAGACAGGGTTTCACCATTTTGGCCAGGCTGGTCTCGAACTCCCGACCT TTTTGTAGTTTTAGTAAAGACAGGGTTTCACCGTTTTGGCCAGGCTGGTCTCGAACTCCCGACCT A G TGIF2,TGIF2-RAB5IF Ensembl:ENSG00000118707,Ensembl:ENSG00000259399 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1027951757 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106038,RMVar_hsa_circ_117136,RMVar_hsa_circ_209863,RMVar_hsa_circ_87911,RMVar_hsa_circ_209865,RMVar_hsa_circ_209866 49648 RMVar_ID_49648 Human_SNP_ID_680082332 A-to-I Human chr20 + 36584747 36584747 36584747 TTTTGTAGTTTTAGTAAAGACAGGGTTTCACCATTTTGGCCAGGCTGGTCTCGAACTCCCGACCT TTTTGTAGTTTTAGTAAAGACAGGGTTTCACCTTTTTGGCCAGGCTGGTCTCGAACTCCCGACCT A T TGIF2,TGIF2-RAB5IF Ensembl:ENSG00000118707,Ensembl:ENSG00000259399 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1027951757 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106038,RMVar_hsa_circ_117136,RMVar_hsa_circ_209863,RMVar_hsa_circ_87911,RMVar_hsa_circ_209865,RMVar_hsa_circ_209866 49649 RMVar_ID_49649 Human_SNP_ID_680082333 A-to-I Human chr20 + 36584756 36584756 36584756 TTTAGTAAAGACAGGGTTTCACCATTTTGGCCAGGCTGGTCTCGAACTCCCGACCTCAGGTGGTC TTTAGTAAAGACAGGGTTTCACCATTTTGGCCGGGCTGGTCTCGAACTCCCGACCTCAGGTGGTC A G TGIF2,TGIF2-RAB5IF Ensembl:ENSG00000118707,Ensembl:ENSG00000259399 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs76703481 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106038,RMVar_hsa_circ_117136,RMVar_hsa_circ_209863,RMVar_hsa_circ_87911,RMVar_hsa_circ_209865,RMVar_hsa_circ_209866 49650 RMVar_ID_49650 Human_SNP_ID_680082372 A-to-I Human chr20 + 36584939 36584939 36584939 TGAACGCAGGCTGGGCACAGTGGCTCACACCTATAATTCCAGCACTTTGGGAGGCCGAGGCAAAC TGAACGCAGGCTGGGCACAGTGGCTCACACCTGTAATTCCAGCACTTTGGGAGGCCGAGGCAAAC A G TGIF2,TGIF2-RAB5IF Ensembl:ENSG00000118707,Ensembl:ENSG00000259399 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs969110850 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106038,RMVar_hsa_circ_117136,RMVar_hsa_circ_209863,RMVar_hsa_circ_87911,RMVar_hsa_circ_209865,RMVar_hsa_circ_209866 49651 RMVar_ID_49651 Human_SNP_ID_680082414 A-to-I Human chr20 + 36585124 36585124 36585124 GAGGCTGAGGCAGGAGAATCACTTTTGAACCTAGGAGGTGGAGATTGCCGTGAGCGAGATCCTGC GAGGCTGAGGCAGGAGAATCACTTTTGAACCTTGGAGGTGGAGATTGCCGTGAGCGAGATCCTGC A T TGIF2,TGIF2-RAB5IF Ensembl:ENSG00000118707,Ensembl:ENSG00000259399 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1302318449 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106038,RMVar_hsa_circ_117136,RMVar_hsa_circ_209863,RMVar_hsa_circ_87911,RMVar_hsa_circ_209865,RMVar_hsa_circ_209866 49652 RMVar_ID_49652 Human_SNP_ID_680083574 A-to-I Human chr20 + 36589448 36589448 36589448 GGAGTCTCACTCTGTTACCCACGCTGGAGTGCAATGGCGTGGTCATGGCTCACTGCAACCTCTGC GGAGTCTCACTCTGTTACCCACGCTGGAGTGCGATGGCGTGGTCATGGCTCACTGCAACCTCTGC A G TGIF2,TGIF2-RAB5IF Ensembl:ENSG00000118707,Ensembl:ENSG00000259399 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1224565928 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106038,RMVar_hsa_circ_117136,RMVar_hsa_circ_209863,RMVar_hsa_circ_87911,RMVar_hsa_circ_209865,RMVar_hsa_circ_209866 49653 RMVar_ID_49653 Human_SNP_ID_680083654 A-to-I Human chr20 + 36589712 36589712 36589712 CACGCTCGACCGACTTTTTTTTTCTTTGAGACAAGGTCTCACGCTGTCACCCAGGCTGGAGTACA CACGCTCGACCGACTTTTTTTTTCTTTGAGACGAGGTCTCACGCTGTCACCCAGGCTGGAGTACA A G TGIF2,TGIF2-RAB5IF Ensembl:ENSG00000118707,Ensembl:ENSG00000259399 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs935507779 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106038,RMVar_hsa_circ_117136,RMVar_hsa_circ_209863,RMVar_hsa_circ_87911,RMVar_hsa_circ_209865,RMVar_hsa_circ_209866 49654 RMVar_ID_49654 Human_SNP_ID_680083688 A-to-I Human chr20 + 36589818 36589818 36589818 TCAATTGATCCTATCACCTCAGCCTCGCAAGTAGCCGAGACTACAGACACGCACCACCATACCCA TCAATTGATCCTATCACCTCAGCCTCGCAAGTGGCCGAGACTACAGACACGCACCACCATACCCA A G TGIF2,TGIF2-RAB5IF Ensembl:ENSG00000118707,Ensembl:ENSG00000259399 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs533042451 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106038,RMVar_hsa_circ_117136,RMVar_hsa_circ_209863,RMVar_hsa_circ_87911,RMVar_hsa_circ_209865,RMVar_hsa_circ_209866 49655 RMVar_ID_49655 Human_SNP_ID_680083948 A-to-I Human chr20 + 36590819 36590819 36590819 GGGCTTAAGCAATCCTCCCGCCTTGGCCACCCAAAGTGTTGGGATTACAGGTGTGAGCCACTGTG GGGCTTAAGCAATCCTCCCGCCTTGGCCACCCGAAGTGTTGGGATTACAGGTGTGAGCCACTGTG A G TGIF2,TGIF2-RAB5IF Ensembl:ENSG00000118707,Ensembl:ENSG00000259399 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1198908537 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106038,RMVar_hsa_circ_117136,RMVar_hsa_circ_209863,RMVar_hsa_circ_87911,RMVar_hsa_circ_209865,RMVar_hsa_circ_209866 49656 RMVar_ID_49656 Human_SNP_ID_680084555 A-to-I Human chr20 + 36592889 36592889 36592889 TCACCCGGGCTGGAGTGCAGTGGTGCGATCTCAGCTCACTGTAACCTCCGCCTCCCGGGTTCAAG TCACCCGGGCTGGAGTGCAGTGGTGCGATCTCGGCTCACTGTAACCTCCGCCTCCCGGGTTCAAG A G TGIF2,TGIF2-RAB5IF Ensembl:ENSG00000118707,Ensembl:ENSG00000259399 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs937626967 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14091889 RMVar_hsa_circ_106038,RMVar_hsa_circ_117136,RMVar_hsa_circ_209863,RMVar_hsa_circ_87911,RMVar_hsa_circ_209865,RMVar_hsa_circ_209866 49657 RMVar_ID_49657 Human_SNP_ID_680089874 A-to-I Human chr20 + 36611045 36611045 36611045 ACAGGCTCACCATTTCACCCAGGCTGTAGTGCAGTGGCGCAGTCTTGGCTCACTGCAGCCTCTGC ACAGGCTCACCATTTCACCCAGGCTGTAGTGCGGTGGCGCAGTCTTGGCTCACTGCAGCCTCTGC A G RAB5IF,TGIF2-RAB5IF Ensembl:ENSG00000101084,Ensembl:ENSG00000259399 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs921110678 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14092050 RMVar_hsa_circ_87911,RMVar_hsa_circ_209866,RMVar_hsa_circ_209868,RMVar_hsa_circ_109383 49658 RMVar_ID_49658 Human_SNP_ID_680089890 A-to-I Human chr20 + 36611119 36611119 36611119 TCAAGTGATCCTCCCACCTCAGCCTCCCGAGTAGTTGGGACTACAGGTGTGAGCCACCATGCCCG TCAAGTGATCCTCCCACCTCAGCCTCCCGAGTGGTTGGGACTACAGGTGTGAGCCACCATGCCCG A G RAB5IF,TGIF2-RAB5IF Ensembl:ENSG00000101084,Ensembl:ENSG00000259399 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1272315287 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_87911,RMVar_hsa_circ_209866,RMVar_hsa_circ_209868,RMVar_hsa_circ_109383 49659 RMVar_ID_49659 Human_SNP_ID_680100713 A-to-I Human chr20 - 36652374 36652374 36652374 CAGAGTCTCGCTGTTACCCAGGCTGGAGTGCAATGGCGCAAACTTGGCTCACTGCAACCTCTGCC CAGAGTCTCGCTGTTACCCAGGCTGGAGTGCAGTGGCGCAAACTTGGCTCACTGCAACCTCTGCC T C NDRG3 Ensembl:ENSG00000101079 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs555164034 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8204550,Human_RBP_ID_26493036 RMVar_hsa_circ_112987,RMVar_hsa_circ_117227,RMVar_hsa_circ_126609,RMVar_hsa_circ_209874,RMVar_hsa_circ_209875,RMVar_hsa_circ_209873 49660 RMVar_ID_49660 Human_SNP_ID_680102210 A-to-I Human chr20 - 36659394 36659394 36659394 GCTGGGCACGGTGGCTCACACCTATAATCCCAACACTTTGGGAGGCTGAGTTGGGCGGATCACTT GCTGGGCACGGTGGCTCACACCTATAATCCCAGCACTTTGGGAGGCTGAGTTGGGCGGATCACTT T C NDRG3 Ensembl:ENSG00000101079 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs973912699 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85223,RMVar_hsa_circ_112987,RMVar_hsa_circ_117227,RMVar_hsa_circ_126609,RMVar_hsa_circ_209874,RMVar_hsa_circ_209875,RMVar_hsa_circ_306003,RMVar_hsa_circ_209873,RMVar_hsa_circ_285604,RMVar_hsa_circ_209878,RMVar_hsa_circ_209876,RMVar_hsa_circ_209877,RMVar_hsa_circ_120876 49661 RMVar_ID_49661 Human_SNP_ID_680129118 A-to-I Human chr20 - 36768339 36768339 36768339 GGGATTTCACCATGTTGTCCAGACTAGTCTCCAGCTCGTGGTCTCAAGTGATCCCATGCCTCGGC GGGATTTCACCATGTTGTCCAGACTAGTCTCCGGCTCGTGGTCTCAAGTGATCCCATGCCTCGGC T C DSN1 Ensembl:ENSG00000149636 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1487347951 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22541 49662 RMVar_ID_49662 Human_SNP_ID_680129120 A-to-I Human chr20 - 36768346 36768346 36768346 TAGAGACGGGATTTCACCATGTTGTCCAGACTAGTCTCCAGCTCGTGGTCTCAAGTGATCCCATG TAGAGACGGGATTTCACCATGTTGTCCAGACTGGTCTCCAGCTCGTGGTCTCAAGTGATCCCATG T C DSN1 Ensembl:ENSG00000149636 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1287730076 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22541 49663 RMVar_ID_49663 Human_SNP_ID_680129595 A-to-I Human chr20 - 36770336 36770336 36770336 GAGTGGGCCAGGCACGGTGCCTCATGCCTATAATCCCAGCACTTTGGGAGGCAGGAGGATTGCTT GAGTGGGCCAGGCACGGTGCCTCATGCCTATAGTCCCAGCACTTTGGGAGGCAGGAGGATTGCTT T C DSN1 Ensembl:ENSG00000149636 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1280999064 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_22541 49664 RMVar_ID_49664 Human_SNP_ID_680129597 A-to-I Human chr20 - 36770339 36770339 36770339 CTAGAGTGGGCCAGGCACGGTGCCTCATGCCTATAATCCCAGCACTTTGGGAGGCAGGAGGATTG CTAGAGTGGGCCAGGCACGGTGCCTCATGCCTGTAATCCCAGCACTTTGGGAGGCAGGAGGATTG T C DSN1 Ensembl:ENSG00000149636 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs749294467 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25630017 RMVar_hsa_circ_22541 49665 RMVar_ID_49665 Human_SNP_ID_680129661 A-to-I Human chr20 - 36770667 36770667 36770667 TTTTTAAGAGACAGGATGTTGCTGTTTTGTCTAGGCTGGACTTGAACTTCTGGGCTCAAGCAATC TTTTTAAGAGACAGGATGTTGCTGTTTTGTCTGGGCTGGACTTGAACTTCTGGGCTCAAGCAATC T C DSN1 Ensembl:ENSG00000149636 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1171991438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6997238,Human_RBP_ID_17571242,Human_RBP_ID_23903216 RMVar_hsa_circ_22541 49666 RMVar_ID_49666 Human_SNP_ID_680130088 A-to-I Human chr20 - 36772295 36772295 36772295 GACAGAGTGAGATTCCACCTCAAAAAAAAACAAAAACAAAGAATAGACTGGAGACGGGCCGTTGG GACAGAGTGAGATTCCACCTCAAAAAAAAACAGAAACAAAGAATAGACTGGAGACGGGCCGTTGG T C DSN1 Ensembl:ENSG00000149636 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs544574071 Functional Loss SNV dbSNP153 33..33 33 - - - 49667 RMVar_ID_49667 Human_SNP_ID_680132186 A-to-I Human chr20 - 36781424 36781424 36781424 TCAAGCAGTTCTCCTGCCTCAACCTCCCGAGTAACTGGGATTACAGGTGTGTGCCACCACACCCG TCAAGCAGTTCTCCTGCCTCAACCTCCCGAGTGACTGGGATTACAGGTGTGTGCCACCACACCCG T C SOGA1 Ensembl:ENSG00000149639 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs768235143 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25608799 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 49668 RMVar_ID_49668 Human_SNP_ID_680132309 A-to-I Human chr20 - 36781911 36781911 36781911 ATCACTTGAACCTGGTGGGGAGCAGCGGTTGCAGTGAGCCGAGATTGTGCCATTGCGCTCTAGCC ATCACTTGAACCTGGTGGGGAGCAGCGGTTGCGGTGAGCCGAGATTGTGCCATTGCGCTCTAGCC T C SOGA1 Ensembl:ENSG00000149639 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,31158229,32596459 RNA-Seq:(High) rs970326260 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14093115 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 49669 RMVar_ID_49669 Human_SNP_ID_680133510 A-to-I Human chr20 - 36787366 36787366 36787366 AAAATTAGCTAGGCATGGTGGCACACGCTTGTAATCTTAGCTACTTGGGAGGCTGAGGCACAAGA AAAATTAGCTAGGCATGGTGGCACACGCTTGTGATCTTAGCTACTTGGGAGGCTGAGGCACAAGA T C SOGA1 Ensembl:ENSG00000149639 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs896586739 Functional Loss SNV dbSNP153 33..33 33 - - - 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 49670 RMVar_ID_49670 Human_SNP_ID_680134097 A-to-I Human chr20 - 36789451 36789451 36789451 CACCATGTTGGCCAGGCTGGTCTCGAACTGCTAATCTCAAGTGATCCGCCTGCCTCAGTCTCCCA CACCATGTTGGCCAGGCTGGTCTCGAACTGCTGATCTCAAGTGATCCGCCTGCCTCAGTCTCCCA T C SOGA1 Ensembl:ENSG00000149639 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2425292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25608818 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 49671 RMVar_ID_49671 Human_SNP_ID_680134131 A-to-I Human chr20 - 36789627 36789627 36789627 GGAGCCTCACTCTGTCACCCAGGTTGGAATGCAGTGGTGTGATCTCGGCTCACTGCAACCTCTGC GGAGCCTCACTCTGTCACCCAGGTTGGAATGCGGTGGTGTGATCTCGGCTCACTGCAACCTCTGC T C SOGA1 Ensembl:ENSG00000149639 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1391237869 Functional Loss SNV dbSNP153 33..33 33 - - - 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 49672 RMVar_ID_49672 Human_SNP_ID_680134852 A-to-I Human chr20 - 36792458 36792458 36792458 TCTTGTCCCCCAGGCTTGAGTGCAATGACTCAATCTCGGCTCACTGTAACCTCCGCCTCCTGGGT TCTTGTCCCCCAGGCTTGAGTGCAATGACTCAGTCTCGGCTCACTGTAACCTCCGCCTCCTGGGT T C SOGA1 Ensembl:ENSG00000149639 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1226376785 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14178601 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 49673 RMVar_ID_49673 Human_SNP_ID_680135057 A-to-I Human chr20 - 36793065 36793065 36793065 CCCCATCTCTACTAAAAATACAAAAATTGGCCAGGCGTGGTGGCATGCACCTGTTGTCCCAGCTG CCCCATCTCTACTAAAAATACAAAAATTGGCCGGGCGTGGTGGCATGCACCTGTTGTCCCAGCTG T C SOGA1 Ensembl:ENSG00000149639 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1461381086 Functional Loss SNV dbSNP153 33..33 33 - - - 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 49674 RMVar_ID_49674 Human_SNP_ID_680135061 A-to-I Human chr20 - 36793080 36793080 36793080 GCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTGGCCAGGCGTGGTGGCATGCAC GCCAACATGGTGAAACCCCATCTCTACTAAAAGTACAAAAATTGGCCAGGCGTGGTGGCATGCAC T C SOGA1 Ensembl:ENSG00000149639 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1017159369 Functional Loss SNV dbSNP153 33..33 33 - - - 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 49675 RMVar_ID_49675 Human_SNP_ID_680138446 A-to-I Human chr20 - 36806702 36806702 36806702 CAGTCTGGTCAACGTGATGAAACCCTGTCTCTACTAAAAATACAAAAATTAGCTGGGAACGGTGG CAGTCTGGTCAACGTGATGAAACCCTGTCTCTGCTAAAAATACAAAAATTAGCTGGGAACGGTGG T C SOGA1 Ensembl:ENSG00000149639 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs983083538 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_209895,RMVar_hsa_circ_88558,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_307256,RMVar_hsa_circ_209903,RMVar_hsa_circ_46774,RMVar_hsa_circ_374332,RMVar_hsa_circ_209905,RMVar_hsa_circ_209906 49676 RMVar_ID_49676 Human_SNP_ID_680142384 A-to-I Human chr20 - 36821610 36821610 36821610 GGGCTCAAGCAATTCTCCCACCTCAGCCTCCCAAGTAGCTAGGACTACAGACACATGCCACAACA GGGCTCAAGCAATTCTCCCACCTCAGCCTCCCCAGTAGCTAGGACTACAGACACATGCCACAACA T G SOGA1 Ensembl:ENSG00000149639 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1160625829 Functional Loss SNV dbSNP153 33..33 33 - - - 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_286292,RMVar_hsa_circ_8303,RMVar_hsa_circ_209908,RMVar_hsa_circ_117868,RMVar_hsa_circ_209910,RMVar_hsa_circ_209909,RMVar_hsa_circ_364603 49677 RMVar_ID_49677 Human_SNP_ID_680142851 A-to-I Human chr20 - 36823777 36823777 36823777 GGAGACAAGAGTCTTGCTGTGTCACTCAGGCTAGAGTGTAGTGGCACGATCATGGTTCATTGCAG GGAGACAAGAGTCTTGCTGTGTCACTCAGGCTGGAGTGTAGTGGCACGATCATGGTTCATTGCAG T C SOGA1 Ensembl:ENSG00000149639 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs550439106 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14093236 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_286292,RMVar_hsa_circ_8303,RMVar_hsa_circ_209908,RMVar_hsa_circ_117868,RMVar_hsa_circ_209910,RMVar_hsa_circ_209909,RMVar_hsa_circ_364603 49678 RMVar_ID_49678 Human_SNP_ID_680146355 A-to-I Human chr20 - 36838251 36838251 36838251 AGTGAAGGCCTCGAGACCATCCTGGCTAATACAGTGAAACCCTGTCTCTACTGAAAACACAAAAA AGTGAAGGCCTCGAGACCATCCTGGCTAATACTGTGAAACCCTGTCTCTACTGAAAACACAAAAA T A SOGA1 Ensembl:ENSG00000149639 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6016573 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_290074,RMVar_hsa_circ_43114,RMVar_hsa_circ_209899,RMVar_hsa_circ_83836,RMVar_hsa_circ_126199,RMVar_hsa_circ_348377,RMVar_hsa_circ_209903,RMVar_hsa_circ_209906,RMVar_hsa_circ_286292,RMVar_hsa_circ_8303,RMVar_hsa_circ_209908,RMVar_hsa_circ_117868,RMVar_hsa_circ_209909,RMVar_hsa_circ_271698,RMVar_hsa_circ_209911 49679 RMVar_ID_49679 Human_SNP_ID_680146356 A-to-I Human chr20 - 36838251 36838251 36838251 AGTGAAGGCCTCGAGACCATCCTGGCTAATACAGTGAAACCCTGTCTCTACTGAAAACACAAAAA AGTGAAGGCCTCGAGACCATCCTGGCTAATACGGTGAAACCCTGTCTCTACTGAAAACACAAAAA T C SOGA1 Ensembl:ENSG00000149639 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs6016573 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_290074,RMVar_hsa_circ_43114,RMVar_hsa_circ_209899,RMVar_hsa_circ_83836,RMVar_hsa_circ_126199,RMVar_hsa_circ_348377,RMVar_hsa_circ_209903,RMVar_hsa_circ_209906,RMVar_hsa_circ_286292,RMVar_hsa_circ_8303,RMVar_hsa_circ_209908,RMVar_hsa_circ_117868,RMVar_hsa_circ_209909,RMVar_hsa_circ_271698,RMVar_hsa_circ_209911 49680 RMVar_ID_49680 Human_SNP_ID_680147179 A-to-I Human chr20 - 36841276 36841276 36841276 CACTCTGTCACCCAATGGTGCAATCTCGGCTCACTGCATCCTCTGCCTCCTAGGTTCAAGTGATT CACTCTGTCACCCAATGGTGCAATCTCGGCTCCCTGCATCCTCTGCCTCCTAGGTTCAAGTGATT T G SOGA1 Ensembl:ENSG00000149639 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1463945380 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126199,RMVar_hsa_circ_209903 49681 RMVar_ID_49681 Human_SNP_ID_680160391 A-to-I Human chr20 - 36890453 36890453 36890453 TCTCAAACAAAAAGAAAGAAAGGAAGGAAGGAAGGAGGGAAGGAAGGAAGGAAAGAGAGAAAGAA TCTCAAACAAAAAGAAAGAAAGGAAGGAAGGAGGGAGGGAAGGAAGGAAGGAAAGAGAGAAAGAA T C SAMHD1 Ensembl:ENSG00000101347 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs889553814 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4645481 49682 RMVar_ID_49682 Human_SNP_ID_680160444 A-to-I Human chr20 - 36890602 36890602 36890602 AAATTAGCCGGGCGTGGTGGTGTGTGCTTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAA AAATTAGCCGGGCGTGGTGGTGTGTGCTTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAA T C SAMHD1 Ensembl:ENSG00000101347 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1129213 Functional Loss SNV dbSNP153 33..33 33 - - - 49683 RMVar_ID_49683 Human_SNP_ID_680166389 A-to-I Human chr20 - 36914955 36914955 36914955 CAGATTGGAGTGTAGTGGTGCGATCTCAGATCACTGCAACCTCCACCTTCCCAGCTCAAGCAAAT CAGATTGGAGTGTAGTGGTGCGATCTCAGATCGCTGCAACCTCCACCTTCCCAGCTCAAGCAAAT T C SAMHD1 Ensembl:ENSG00000101347 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs139922523 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16102,RMVar_hsa_circ_36364,RMVar_hsa_circ_65041,RMVar_hsa_circ_58533,RMVar_hsa_circ_209918,RMVar_hsa_circ_209916,RMVar_hsa_circ_209917,RMVar_hsa_circ_79131,RMVar_hsa_circ_209920,RMVar_hsa_circ_269754,RMVar_hsa_circ_320752,RMVar_hsa_circ_352205,RMVar_hsa_circ_209921,RMVar_hsa_circ_266274 49684 RMVar_ID_49684 Human_SNP_ID_680166391 A-to-I Human chr20 - 36914960 36914960 36914960 TCACCCAGATTGGAGTGTAGTGGTGCGATCTCAGATCACTGCAACCTCCACCTTCCCAGCTCAAG TCACCCAGATTGGAGTGTAGTGGTGCGATCTCCGATCACTGCAACCTCCACCTTCCCAGCTCAAG T G SAMHD1 Ensembl:ENSG00000101347 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1465470740 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16102,RMVar_hsa_circ_36364,RMVar_hsa_circ_65041,RMVar_hsa_circ_58533,RMVar_hsa_circ_209918,RMVar_hsa_circ_209916,RMVar_hsa_circ_209917,RMVar_hsa_circ_79131,RMVar_hsa_circ_209920,RMVar_hsa_circ_269754,RMVar_hsa_circ_320752,RMVar_hsa_circ_352205,RMVar_hsa_circ_209921,RMVar_hsa_circ_266274 49685 RMVar_ID_49685 Human_SNP_ID_680166402 A-to-I Human chr20 - 36914998 36914998 36914998 ATTCTTTTTTTTCTTTTTGGATACAGGATCTTACTCTGTCACCCAGATTGGAGTGTAGTGGTGCG ATTCTTTTTTTTCTTTTTGGATACAGGATCTTTCTCTGTCACCCAGATTGGAGTGTAGTGGTGCG T A SAMHD1 Ensembl:ENSG00000101347 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs571245756 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16102,RMVar_hsa_circ_36364,RMVar_hsa_circ_65041,RMVar_hsa_circ_58533,RMVar_hsa_circ_209918,RMVar_hsa_circ_209916,RMVar_hsa_circ_209917,RMVar_hsa_circ_79131,RMVar_hsa_circ_209920,RMVar_hsa_circ_269754,RMVar_hsa_circ_320752,RMVar_hsa_circ_352205,RMVar_hsa_circ_209921,RMVar_hsa_circ_266274 49686 RMVar_ID_49686 Human_SNP_ID_680187677 A-to-I Human chr20 - 36996581 36996581 36996581 AAAATTAGTTGGGTGTGATGGCATGTGCCTGTAGTCCCAGCTACTCAGGAGACTGACATGAGAGG AAAATTAGTTGGGTGTGATGGCATGTGCCTGTCGTCCCAGCTACTCAGGAGACTGACATGAGAGG T G RBL1 Ensembl:ENSG00000080839 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1342271179 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_563421 49687 RMVar_ID_49687 Human_SNP_ID_680187680 A-to-I Human chr20 - 36996591 36996591 36996591 AAAAAATAAAAAAATTAGTTGGGTGTGATGGCATGTGCCTGTAGTCCCAGCTACTCAGGAGACTG AAAAAATAAAAAAATTAGTTGGGTGTGATGGCTTGTGCCTGTAGTCCCAGCTACTCAGGAGACTG T A RBL1 Ensembl:ENSG00000080839 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388230808 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_563421 49688 RMVar_ID_49688 Human_SNP_ID_680190686 A-to-I Human chr20 - 37005319 37005316 37005320 TCACTGCAACCTCTGCCTCCTGGGTTCAGGCAATTCTGTAACTCAGCCTCCTGAGTAGCTGGCAT TCACTGCAACCTCTGCCTCCTGGGTTCAGGC____CTGTAACTCAGCCTCCTGAGTAGCTGGCAT GAATT G RBL1 Ensembl:ENSG00000080839 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1373413878 Functional Loss DEL dbSNP153 32..35 33 - - - RMVar_hsa_circ_13479,RMVar_hsa_circ_67230,RMVar_hsa_circ_90911,RMVar_hsa_circ_307093,RMVar_hsa_circ_359446,RMVar_hsa_circ_209929,RMVar_hsa_circ_331711,RMVar_hsa_circ_288671,RMVar_hsa_circ_34810,RMVar_hsa_circ_64116,RMVar_hsa_circ_25674,RMVar_hsa_circ_209931,RMVar_hsa_circ_12152,RMVar_hsa_circ_209932,RMVar_hsa_circ_209930 49689 RMVar_ID_49689 Human_SNP_ID_680190688 A-to-I Human chr20 - 37005319 37005319 37005319 TCACTGCAACCTCTGCCTCCTGGGTTCAGGCAATTCTGTAACTCAGCCTCCTGAGTAGCTGGCAT TCACTGCAACCTCTGCCTCCTGGGTTCAGGCAGTTCTGTAACTCAGCCTCCTGAGTAGCTGGCAT T C RBL1 Ensembl:ENSG00000080839 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs758055466 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13479,RMVar_hsa_circ_67230,RMVar_hsa_circ_90911,RMVar_hsa_circ_307093,RMVar_hsa_circ_359446,RMVar_hsa_circ_209929,RMVar_hsa_circ_331711,RMVar_hsa_circ_288671,RMVar_hsa_circ_34810,RMVar_hsa_circ_64116,RMVar_hsa_circ_25674,RMVar_hsa_circ_209931,RMVar_hsa_circ_12152,RMVar_hsa_circ_209932,RMVar_hsa_circ_209930 49690 RMVar_ID_49690 Human_SNP_ID_680190693 A-to-I Human chr20 - 37005359 37005359 37005359 TCTGTTGCCCAGGCTGGAGTGCAAGTGGCACAATCTCAGCTCACTGCAACCTCTGCCTCCTGGGT TCTGTTGCCCAGGCTGGAGTGCAAGTGGCACAGTCTCAGCTCACTGCAACCTCTGCCTCCTGGGT T C RBL1 Ensembl:ENSG00000080839 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1157284066 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13479,RMVar_hsa_circ_67230,RMVar_hsa_circ_90911,RMVar_hsa_circ_307093,RMVar_hsa_circ_359446,RMVar_hsa_circ_209929,RMVar_hsa_circ_331711,RMVar_hsa_circ_288671,RMVar_hsa_circ_34810,RMVar_hsa_circ_64116,RMVar_hsa_circ_25674,RMVar_hsa_circ_209931,RMVar_hsa_circ_12152,RMVar_hsa_circ_209932,RMVar_hsa_circ_209930 49691 RMVar_ID_49691 Human_SNP_ID_680191192 A-to-I Human chr20 - 37007218 37007218 37007218 CAGAGGAAATCATGGGATCTGTTGCCCAGGCTAGAGTGCAGTGGCGAGATCTGGGCTCACTGCAA CAGAGGAAATCATGGGATCTGTTGCCCAGGCTGGAGTGCAGTGGCGAGATCTGGGCTCACTGCAA T C RBL1 Ensembl:ENSG00000080839 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1357937627 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13479,RMVar_hsa_circ_67230,RMVar_hsa_circ_90911,RMVar_hsa_circ_307093,RMVar_hsa_circ_359446,RMVar_hsa_circ_209929,RMVar_hsa_circ_331711,RMVar_hsa_circ_288671,RMVar_hsa_circ_34810,RMVar_hsa_circ_64116,RMVar_hsa_circ_25674,RMVar_hsa_circ_209931,RMVar_hsa_circ_12152,RMVar_hsa_circ_209932,RMVar_hsa_circ_209930 49692 RMVar_ID_49692 Human_SNP_ID_680194076 A-to-I Human chr20 - 37017219 37017219 37017219 GCAGGCATGCACCATCACCCTGGCGAATTTTTATATTTTTTGTAGAGACGGGATTTTGCCATGTT GCAGGCATGCACCATCACCCTGGCGAATTTTTTTATTTTTTGTAGAGACGGGATTTTGCCATGTT T A RBL1 Ensembl:ENSG00000080839 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs981294467 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13479,RMVar_hsa_circ_67230,RMVar_hsa_circ_90911,RMVar_hsa_circ_307093,RMVar_hsa_circ_359446,RMVar_hsa_circ_209929,RMVar_hsa_circ_331711,RMVar_hsa_circ_34810,RMVar_hsa_circ_64116,RMVar_hsa_circ_25674,RMVar_hsa_circ_209934,RMVar_hsa_circ_51658,RMVar_hsa_circ_209931,RMVar_hsa_circ_12152,RMVar_hsa_circ_209932,RMVar_hsa_circ_280469,RMVar_hsa_circ_338097,RMVar_hsa_circ_306796,RMVar_hsa_circ_280412,RMVar_hsa_circ_11736,RMVar_hsa_circ_209935,RMVar_hsa_circ_209936,RMVar_hsa_circ_209933 49693 RMVar_ID_49693 Human_SNP_ID_680196437 A-to-I Human chr20 - 37027308 37027308 37027308 TTGAGACAGGGTCTTGCTCTGTCGCCCAGACTAGAGTGCATAGGCACGATCATGTCTCACTGCAG TTGAGACAGGGTCTTGCTCTGTCGCCCAGACTGGAGTGCATAGGCACGATCATGTCTCACTGCAG T C RBL1 Ensembl:ENSG00000080839 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs932529409 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13479,RMVar_hsa_circ_67230,RMVar_hsa_circ_90911,RMVar_hsa_circ_359446,RMVar_hsa_circ_209929,RMVar_hsa_circ_331711,RMVar_hsa_circ_64116,RMVar_hsa_circ_25674,RMVar_hsa_circ_51658,RMVar_hsa_circ_12152,RMVar_hsa_circ_209932,RMVar_hsa_circ_280469,RMVar_hsa_circ_338097,RMVar_hsa_circ_11736,RMVar_hsa_circ_209935,RMVar_hsa_circ_209936,RMVar_hsa_circ_26555,RMVar_hsa_circ_335119,RMVar_hsa_circ_346376,RMVar_hsa_circ_323485,RMVar_hsa_circ_39253,RMVar_hsa_circ_287710,RMVar_hsa_circ_27619,RMVar_hsa_circ_209939,RMVar_hsa_circ_20076,RMVar_hsa_circ_209937,RMVar_hsa_circ_330048,RMVar_hsa_circ_318043,RMVar_hsa_circ_364436,RMVar_hsa_circ_312297 49694 RMVar_ID_49694 Human_SNP_ID_680196622 A-to-I Human chr20 - 37028327 37028327 37028327 ACAGTCTTACTCTGTCTACCAAGCTGGAATGCAGTAGCGTGATCTCGGCTCACTACAGCTTCTGT ACAGTCTTACTCTGTCTACCAAGCTGGAATGCCGTAGCGTGATCTCGGCTCACTACAGCTTCTGT T G RBL1 Ensembl:ENSG00000080839 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1314252602 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13479,RMVar_hsa_circ_67230,RMVar_hsa_circ_90911,RMVar_hsa_circ_359446,RMVar_hsa_circ_209929,RMVar_hsa_circ_331711,RMVar_hsa_circ_64116,RMVar_hsa_circ_25674,RMVar_hsa_circ_51658,RMVar_hsa_circ_12152,RMVar_hsa_circ_209932,RMVar_hsa_circ_280469,RMVar_hsa_circ_338097,RMVar_hsa_circ_11736,RMVar_hsa_circ_209935,RMVar_hsa_circ_209936,RMVar_hsa_circ_26555,RMVar_hsa_circ_335119,RMVar_hsa_circ_346376,RMVar_hsa_circ_323485,RMVar_hsa_circ_39253,RMVar_hsa_circ_287710,RMVar_hsa_circ_27619,RMVar_hsa_circ_209939,RMVar_hsa_circ_20076,RMVar_hsa_circ_209937,RMVar_hsa_circ_330048,RMVar_hsa_circ_318043,RMVar_hsa_circ_364436,RMVar_hsa_circ_312297 49695 RMVar_ID_49695 Human_SNP_ID_680200114 A-to-I Human chr20 - 37042815 37042815 37042815 GGCTCACTGCAGCCTCAACCTCCCAGGCACAAATGATCTCCCCACAGCCTTCTGAGTAGCTGGGA GGCTCACTGCAGCCTCAACCTCCCAGGCACAAGTGATCTCCCCACAGCCTTCTGAGTAGCTGGGA T C RBL1 Ensembl:ENSG00000080839 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs572262851 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8532493,Human_RBP_ID_14094231 RMVar_hsa_circ_67230,RMVar_hsa_circ_90911,RMVar_hsa_circ_359446,RMVar_hsa_circ_209929,RMVar_hsa_circ_331711,RMVar_hsa_circ_25674,RMVar_hsa_circ_21417,RMVar_hsa_circ_209932,RMVar_hsa_circ_11736,RMVar_hsa_circ_335119,RMVar_hsa_circ_323485,RMVar_hsa_circ_287710,RMVar_hsa_circ_27619,RMVar_hsa_circ_209939,RMVar_hsa_circ_20076,RMVar_hsa_circ_364436,RMVar_hsa_circ_312297,RMVar_hsa_circ_286688,RMVar_hsa_circ_46972,RMVar_hsa_circ_21420,RMVar_hsa_circ_41974,RMVar_hsa_circ_271347,RMVar_hsa_circ_209940,RMVar_hsa_circ_319819,RMVar_hsa_circ_342854,RMVar_hsa_circ_18222,RMVar_hsa_circ_337822,RMVar_hsa_circ_278956,RMVar_hsa_circ_301925,RMVar_hsa_circ_71899,RMVar_hsa_circ_94287,RMVar_hsa_circ_44992,RMVar_hsa_circ_209942,RMVar_hsa_circ_209944,RMVar_hsa_circ_40455,RMVar_hsa_circ_209945,RMVar_hsa_circ_209943,RMVar_hsa_circ_209941 49696 RMVar_ID_49696 Human_SNP_ID_680205667 A-to-I Human chr20 - 37064493 37064493 37064493 GCAATCCTCTCACCATAGCCTCCCAAAGTGCTAGGATTACAGGTATGACCCACCACACCCGGCCA GCAATCCTCTCACCATAGCCTCCCAAAGTGCTGGGATTACAGGTATGACCCACCACACCCGGCCA T C RBL1 Ensembl:ENSG00000080839 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1456702956 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67230,RMVar_hsa_circ_25674,RMVar_hsa_circ_2166,RMVar_hsa_circ_21417,RMVar_hsa_circ_287710,RMVar_hsa_circ_20076,RMVar_hsa_circ_364436,RMVar_hsa_circ_21420,RMVar_hsa_circ_41974,RMVar_hsa_circ_342854,RMVar_hsa_circ_18222,RMVar_hsa_circ_301925,RMVar_hsa_circ_209944,RMVar_hsa_circ_40455,RMVar_hsa_circ_209945,RMVar_hsa_circ_348616,RMVar_hsa_circ_333946,RMVar_hsa_circ_3961,RMVar_hsa_circ_209948,RMVar_hsa_circ_371616,RMVar_hsa_circ_276336,RMVar_hsa_circ_33521,RMVar_hsa_circ_209949,RMVar_hsa_circ_209950,RMVar_hsa_circ_282048,RMVar_hsa_circ_298214,RMVar_hsa_circ_62215,RMVar_hsa_circ_209953,RMVar_hsa_circ_209954,RMVar_hsa_circ_305062,RMVar_hsa_circ_289558,RMVar_hsa_circ_209956,RMVar_hsa_circ_209957,RMVar_hsa_circ_281149,RMVar_hsa_circ_309115,RMVar_hsa_circ_66578,RMVar_hsa_circ_209959,RMVar_hsa_circ_209960 49697 RMVar_ID_49697 Human_SNP_ID_680211138 A-to-I Human chr20 - 37085792 37085792 37085792 ACAAAAACAAAATTAGCCAGGTGGGCGCCTGTAGTCCCAGCTACTCGAGAGGCTGAGGTGGGAGT ACAAAAACAAAATTAGCCAGGTGGGCGCCTGTGGTCCCAGCTACTCGAGAGGCTGAGGTGGGAGT T C RBL1 Ensembl:ENSG00000080839 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1288490799 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41974,RMVar_hsa_circ_371616,RMVar_hsa_circ_209949,RMVar_hsa_circ_209954,RMVar_hsa_circ_75016,RMVar_hsa_circ_324487 49698 RMVar_ID_49698 Human_SNP_ID_680212303 A-to-I Human chr20 - 37090838 37090838 37090838 CAGTGATGGACCACACATACTTTATTTTTACTATATGTTTTCTGTGTTTAGATACACAAATAATT CAGTGATGGACCACACATACTTTATTTTTACTGTATGTTTTCTGTGTTTAGATACACAAATAATT T C RBL1 Ensembl:ENSG00000080839 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1191556614 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14094581 49699 RMVar_ID_49699 Human_SNP_ID_680212304 A-to-I Human chr20 - 37090838 37090838 37090838 CAGTGATGGACCACACATACTTTATTTTTACTATATGTTTTCTGTGTTTAGATACACAAATAATT CAGTGATGGACCACACATACTTTATTTTTACTCTATGTTTTCTGTGTTTAGATACACAAATAATT T G RBL1 Ensembl:ENSG00000080839 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1191556614 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14094581 49700 RMVar_ID_49700 Human_SNP_ID_680212885 A-to-I Human chr20 - 37093446 37093446 37093446 TTTGTGGAGATAGTATCTGACTATGTTGCCCAAGCTGGTCTTGAACTGGCCTCAAGTGATTTTTC TTTGTGGAGATAGTATCTGACTATGTTGCCCACGCTGGTCTTGAACTGGCCTCAAGTGATTTTTC T G RBL1 Ensembl:ENSG00000080839 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs920341464 Functional Loss SNV dbSNP153 33..33 33 - - - 49701 RMVar_ID_49701 Human_SNP_ID_680213186 A-to-I Human chr20 - 37094735 37094735 37094735 CTACTCGGGAGGCTGAGGCAGGAGAATTGCTTAAACCCAGGAGGCATAGGCCGCAGTGAGTGGAG CTACTCGGGAGGCTGAGGCAGGAGAATTGCTTGAACCCAGGAGGCATAGGCCGCAGTGAGTGGAG T C RBL1 Ensembl:ENSG00000080839 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs775976237 Functional Loss SNV dbSNP153 33..33 33 - - - 49702 RMVar_ID_49702 Human_SNP_ID_680233742 A-to-I Human chr20 - 37175711 37175711 37175711 ATCTTGCCTCAGCCTCCTGAGTAGCTAGGACTACAGGCACATGCCACCACACCTAGCTAATTTTT ATCTTGCCTCAGCCTCCTGAGTAGCTAGGACTGCAGGCACATGCCACCACACCTAGCTAATTTTT T C MROH8 Ensembl:ENSG00000101353 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs959549855 Functional Loss SNV dbSNP153 33..33 33 - - - 49703 RMVar_ID_49703 Human_SNP_ID_680234629 A-to-I Human chr20 - 37179131 37179131 37179131 GTCCTCCCGCTCACAGGGCCTTGCAGTTCCCGAGGACAGACCCGCCTCTCCCCCGCGCCCAGGCC GTCCTCCCGCTCACAGGGCCTTGCAGTTCCCGGGGACAGACCCGCCTCTCCCCCGCGCCCAGGCC T C MROH8 Ensembl:ENSG00000101353 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs563329951 Functional Loss SNV dbSNP153 33..33 33 - - - 49704 RMVar_ID_49704 Human_SNP_ID_680236285 A-to-I Human chr20 + 37184737 37184737 37184737 TCGTGTGAACCCAGGAGGCAGAGGTTGCAGTGAGCTGAGATCCCGCCATTGCACTCCAGCCCAGG TCGTGTGAACCCAGGAGGCAGAGGTTGCAGTGGGCTGAGATCCCGCCATTGCACTCCAGCCCAGG A G RPN2 Ensembl:ENSG00000118705 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904265081 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14094689,Human_RBP_ID_23001896 RMVar_hsa_circ_90832,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_209982,RMVar_hsa_circ_209980,RMVar_hsa_circ_209977,RMVar_hsa_circ_209978,RMVar_hsa_circ_209976,RMVar_hsa_circ_209973,RMVar_hsa_circ_209974 49705 RMVar_ID_49705 Human_SNP_ID_680241974 A-to-I Human chr20 + 37207847 37207847 37207847 GGGATCACAGGCGCACACCACCATGCCTAGCTAATTTTTGCATTTTTAGTAGAGATGGGGTTTTG GGGATCACAGGCGCACACCACCATGCCTAGCTTATTTTTGCATTTTTAGTAGAGATGGGGTTTTG A T RPN2 Ensembl:ENSG00000118705 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1166565672 Functional Loss SNV dbSNP153 33..33 33 - - - 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_84350,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_317295,RMVar_hsa_circ_287729,RMVar_hsa_circ_127936,RMVar_hsa_circ_84822,RMVar_hsa_circ_209991,RMVar_hsa_circ_105585,RMVar_hsa_circ_209987,RMVar_hsa_circ_209989,RMVar_hsa_circ_209990,RMVar_hsa_circ_209988,RMVar_hsa_circ_209986,RMVar_hsa_circ_79324,RMVar_hsa_circ_83789,RMVar_hsa_circ_209992,RMVar_hsa_circ_209993,RMVar_hsa_circ_277152,RMVar_hsa_circ_209994,RMVar_hsa_circ_325585,RMVar_hsa_circ_327066,RMVar_hsa_circ_371408,RMVar_hsa_circ_284913,RMVar_hsa_circ_87434,RMVar_hsa_circ_124005,RMVar_hsa_circ_81656,RMVar_hsa_circ_92579,RMVar_hsa_circ_209999,RMVar_hsa_circ_12184,RMVar_hsa_circ_210001,RMVar_hsa_circ_210002,RMVar_hsa_circ_210000,RMVar_hsa_circ_209997,RMVar_hsa_circ_209998,RMVar_hsa_circ_210004,RMVar_hsa_circ_92972,RMVar_hsa_circ_115210,RMVar_hsa_circ_345349,RMVar_hsa_circ_210005,RMVar_hsa_circ_124119,RMVar_hsa_circ_324320,RMVar_hsa_circ_210003,RMVar_hsa_circ_288640,RMVar_hsa_circ_120583,RMVar_hsa_circ_210008,RMVar_hsa_circ_210012,RMVar_hsa_circ_88477,RMVar_hsa_circ_91985,RMVar_hsa_circ_210014,RMVar_hsa_circ_76115,RMVar_hsa_circ_210013,RMVar_hsa_circ_210010,RMVar_hsa_circ_210011,RMVar_hsa_circ_210009,RMVar_hsa_circ_210007 49706 RMVar_ID_49706 Human_SNP_ID_680241988 A-to-I Human chr20 + 37207932 37207932 37207932 TTGAACTCCTAGCCTCCCAAAGTGCTGAGATTACAGGTATGAGCCACTGTGCCTGGCCTCTCCCT TTGAACTCCTAGCCTCCCAAAGTGCTGAGATTGCAGGTATGAGCCACTGTGCCTGGCCTCTCCCT A G RPN2 Ensembl:ENSG00000118705 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1030946415 Functional Loss SNV dbSNP153 33..33 33 - - - 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_84350,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_317295,RMVar_hsa_circ_287729,RMVar_hsa_circ_127936,RMVar_hsa_circ_84822,RMVar_hsa_circ_209991,RMVar_hsa_circ_105585,RMVar_hsa_circ_209987,RMVar_hsa_circ_209989,RMVar_hsa_circ_209990,RMVar_hsa_circ_209988,RMVar_hsa_circ_209986,RMVar_hsa_circ_79324,RMVar_hsa_circ_83789,RMVar_hsa_circ_209992,RMVar_hsa_circ_209993,RMVar_hsa_circ_277152,RMVar_hsa_circ_209994,RMVar_hsa_circ_325585,RMVar_hsa_circ_327066,RMVar_hsa_circ_371408,RMVar_hsa_circ_284913,RMVar_hsa_circ_87434,RMVar_hsa_circ_124005,RMVar_hsa_circ_81656,RMVar_hsa_circ_92579,RMVar_hsa_circ_209999,RMVar_hsa_circ_12184,RMVar_hsa_circ_210001,RMVar_hsa_circ_210002,RMVar_hsa_circ_210000,RMVar_hsa_circ_209997,RMVar_hsa_circ_209998,RMVar_hsa_circ_210004,RMVar_hsa_circ_92972,RMVar_hsa_circ_115210,RMVar_hsa_circ_345349,RMVar_hsa_circ_210005,RMVar_hsa_circ_124119,RMVar_hsa_circ_324320,RMVar_hsa_circ_210003,RMVar_hsa_circ_288640,RMVar_hsa_circ_120583,RMVar_hsa_circ_210008,RMVar_hsa_circ_210012,RMVar_hsa_circ_88477,RMVar_hsa_circ_91985,RMVar_hsa_circ_210014,RMVar_hsa_circ_76115,RMVar_hsa_circ_210013,RMVar_hsa_circ_210010,RMVar_hsa_circ_210011,RMVar_hsa_circ_210009,RMVar_hsa_circ_210007 49707 RMVar_ID_49707 Human_SNP_ID_680242731 A-to-I Human chr20 + 37210911 37210911 37210911 GTAAATAAATTTTAAAAATTCAGTTAAGGGCCAGGCATGGGGCTCATACCTGTAACCCCAGCACT GTAAATAAATTTTAAAAATTCAGTTAAGGGCCGGGCATGGGGCTCATACCTGTAACCCCAGCACT A G RPN2 Ensembl:ENSG00000118705 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1314208999 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6997874,Human_RBP_ID_14095222,Human_RBP_ID_17571608 RMVar_hsa_circ_14258,RMVar_hsa_circ_209971,RMVar_hsa_circ_124357,RMVar_hsa_circ_95263,RMVar_hsa_circ_209972,RMVar_hsa_circ_123174,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_84350,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_317295,RMVar_hsa_circ_127936,RMVar_hsa_circ_84822,RMVar_hsa_circ_209991,RMVar_hsa_circ_105585,RMVar_hsa_circ_209987,RMVar_hsa_circ_209989,RMVar_hsa_circ_209990,RMVar_hsa_circ_209988,RMVar_hsa_circ_79324,RMVar_hsa_circ_83789,RMVar_hsa_circ_209992,RMVar_hsa_circ_209993,RMVar_hsa_circ_327066,RMVar_hsa_circ_371408,RMVar_hsa_circ_284913,RMVar_hsa_circ_87434,RMVar_hsa_circ_124005,RMVar_hsa_circ_81656,RMVar_hsa_circ_92579,RMVar_hsa_circ_209999,RMVar_hsa_circ_12184,RMVar_hsa_circ_210001,RMVar_hsa_circ_210002,RMVar_hsa_circ_210000,RMVar_hsa_circ_209998,RMVar_hsa_circ_210004,RMVar_hsa_circ_92972,RMVar_hsa_circ_115210,RMVar_hsa_circ_124119,RMVar_hsa_circ_324320,RMVar_hsa_circ_210003,RMVar_hsa_circ_120583,RMVar_hsa_circ_210008,RMVar_hsa_circ_210012,RMVar_hsa_circ_88477,RMVar_hsa_circ_91985,RMVar_hsa_circ_210014,RMVar_hsa_circ_76115,RMVar_hsa_circ_210013,RMVar_hsa_circ_210010,RMVar_hsa_circ_210011,RMVar_hsa_circ_210009,RMVar_hsa_circ_113989,RMVar_hsa_circ_210016 49708 RMVar_ID_49708 Human_SNP_ID_680242732 A-to-I Human chr20 + 37210915 37210915 37210915 ATAAATTTTAAAAATTCAGTTAAGGGCCAGGCATGGGGCTCATACCTGTAACCCCAGCACTTTAG ATAAATTTTAAAAATTCAGTTAAGGGCCAGGCGTGGGGCTCATACCTGTAACCCCAGCACTTTAG A G RPN2 Ensembl:ENSG00000118705 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1035644485 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6997874,Human_RBP_ID_17571608 RMVar_hsa_circ_14258,RMVar_hsa_circ_209971,RMVar_hsa_circ_124357,RMVar_hsa_circ_95263,RMVar_hsa_circ_209972,RMVar_hsa_circ_123174,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_84350,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_317295,RMVar_hsa_circ_127936,RMVar_hsa_circ_84822,RMVar_hsa_circ_209991,RMVar_hsa_circ_105585,RMVar_hsa_circ_209987,RMVar_hsa_circ_209989,RMVar_hsa_circ_209990,RMVar_hsa_circ_209988,RMVar_hsa_circ_79324,RMVar_hsa_circ_83789,RMVar_hsa_circ_209992,RMVar_hsa_circ_209993,RMVar_hsa_circ_327066,RMVar_hsa_circ_371408,RMVar_hsa_circ_284913,RMVar_hsa_circ_87434,RMVar_hsa_circ_124005,RMVar_hsa_circ_81656,RMVar_hsa_circ_92579,RMVar_hsa_circ_209999,RMVar_hsa_circ_12184,RMVar_hsa_circ_210001,RMVar_hsa_circ_210002,RMVar_hsa_circ_210000,RMVar_hsa_circ_209998,RMVar_hsa_circ_210004,RMVar_hsa_circ_92972,RMVar_hsa_circ_115210,RMVar_hsa_circ_124119,RMVar_hsa_circ_324320,RMVar_hsa_circ_210003,RMVar_hsa_circ_120583,RMVar_hsa_circ_210008,RMVar_hsa_circ_210012,RMVar_hsa_circ_88477,RMVar_hsa_circ_91985,RMVar_hsa_circ_210014,RMVar_hsa_circ_76115,RMVar_hsa_circ_210013,RMVar_hsa_circ_210010,RMVar_hsa_circ_210011,RMVar_hsa_circ_210009,RMVar_hsa_circ_113989,RMVar_hsa_circ_210016 49709 RMVar_ID_49709 Human_SNP_ID_680243030 A-to-I Human chr20 + 37211921 37211921 37211921 CACCATGCCCGGCTAATTTTCGTATTTTCGGTAGAGATGGGGTTTTACCATGTTGGCCAGGCTGG CACCATGCCCGGCTAATTTTCGTATTTTCGGTGGAGATGGGGTTTTACCATGTTGGCCAGGCTGG A G RPN2 Ensembl:ENSG00000118705 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs998733563 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14258,RMVar_hsa_circ_209971,RMVar_hsa_circ_124357,RMVar_hsa_circ_95263,RMVar_hsa_circ_209972,RMVar_hsa_circ_123174,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_84350,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_317295,RMVar_hsa_circ_127936,RMVar_hsa_circ_84822,RMVar_hsa_circ_209991,RMVar_hsa_circ_105585,RMVar_hsa_circ_209987,RMVar_hsa_circ_209989,RMVar_hsa_circ_209990,RMVar_hsa_circ_209988,RMVar_hsa_circ_79324,RMVar_hsa_circ_83789,RMVar_hsa_circ_209992,RMVar_hsa_circ_209993,RMVar_hsa_circ_327066,RMVar_hsa_circ_371408,RMVar_hsa_circ_284913,RMVar_hsa_circ_87434,RMVar_hsa_circ_124005,RMVar_hsa_circ_81656,RMVar_hsa_circ_92579,RMVar_hsa_circ_209999,RMVar_hsa_circ_12184,RMVar_hsa_circ_210001,RMVar_hsa_circ_210002,RMVar_hsa_circ_210000,RMVar_hsa_circ_209998,RMVar_hsa_circ_210004,RMVar_hsa_circ_92972,RMVar_hsa_circ_115210,RMVar_hsa_circ_124119,RMVar_hsa_circ_324320,RMVar_hsa_circ_210003,RMVar_hsa_circ_120583,RMVar_hsa_circ_210008,RMVar_hsa_circ_210012,RMVar_hsa_circ_88477,RMVar_hsa_circ_91985,RMVar_hsa_circ_210014,RMVar_hsa_circ_76115,RMVar_hsa_circ_210013,RMVar_hsa_circ_210010,RMVar_hsa_circ_210011,RMVar_hsa_circ_210009,RMVar_hsa_circ_113989,RMVar_hsa_circ_210016 49710 RMVar_ID_49710 Human_SNP_ID_680243088 A-to-I Human chr20 + 37212156 37212156 37212156 AAGGCCCAGTTTACTGGGTGTGTGGCTTGCCTATAGTTCCAGCTACTTGGGAGGCTGAGGTGGGA AAGGCCCAGTTTACTGGGTGTGTGGCTTGCCTGTAGTTCCAGCTACTTGGGAGGCTGAGGTGGGA A G RPN2 Ensembl:ENSG00000118705 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1234053647 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571609 RMVar_hsa_circ_14258,RMVar_hsa_circ_209971,RMVar_hsa_circ_124357,RMVar_hsa_circ_95263,RMVar_hsa_circ_209972,RMVar_hsa_circ_123174,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_84350,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_317295,RMVar_hsa_circ_127936,RMVar_hsa_circ_84822,RMVar_hsa_circ_209991,RMVar_hsa_circ_105585,RMVar_hsa_circ_209987,RMVar_hsa_circ_209989,RMVar_hsa_circ_209990,RMVar_hsa_circ_209988,RMVar_hsa_circ_79324,RMVar_hsa_circ_83789,RMVar_hsa_circ_209992,RMVar_hsa_circ_209993,RMVar_hsa_circ_327066,RMVar_hsa_circ_371408,RMVar_hsa_circ_284913,RMVar_hsa_circ_87434,RMVar_hsa_circ_124005,RMVar_hsa_circ_81656,RMVar_hsa_circ_92579,RMVar_hsa_circ_209999,RMVar_hsa_circ_12184,RMVar_hsa_circ_210001,RMVar_hsa_circ_210002,RMVar_hsa_circ_210000,RMVar_hsa_circ_209998,RMVar_hsa_circ_210004,RMVar_hsa_circ_92972,RMVar_hsa_circ_115210,RMVar_hsa_circ_124119,RMVar_hsa_circ_324320,RMVar_hsa_circ_210003,RMVar_hsa_circ_120583,RMVar_hsa_circ_210008,RMVar_hsa_circ_210012,RMVar_hsa_circ_88477,RMVar_hsa_circ_91985,RMVar_hsa_circ_210014,RMVar_hsa_circ_76115,RMVar_hsa_circ_210013,RMVar_hsa_circ_210010,RMVar_hsa_circ_210011,RMVar_hsa_circ_210009,RMVar_hsa_circ_113989,RMVar_hsa_circ_210016 49711 RMVar_ID_49711 Human_SNP_ID_680243089 A-to-I Human chr20 + 37212158 37212158 37212158 GGCCCAGTTTACTGGGTGTGTGGCTTGCCTATAGTTCCAGCTACTTGGGAGGCTGAGGTGGGAGG GGCCCAGTTTACTGGGTGTGTGGCTTGCCTATGGTTCCAGCTACTTGGGAGGCTGAGGTGGGAGG A G RPN2 Ensembl:ENSG00000118705 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs760457478 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571609 RMVar_hsa_circ_14258,RMVar_hsa_circ_209971,RMVar_hsa_circ_124357,RMVar_hsa_circ_95263,RMVar_hsa_circ_209972,RMVar_hsa_circ_123174,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_84350,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_317295,RMVar_hsa_circ_127936,RMVar_hsa_circ_84822,RMVar_hsa_circ_209991,RMVar_hsa_circ_105585,RMVar_hsa_circ_209987,RMVar_hsa_circ_209989,RMVar_hsa_circ_209990,RMVar_hsa_circ_209988,RMVar_hsa_circ_79324,RMVar_hsa_circ_83789,RMVar_hsa_circ_209992,RMVar_hsa_circ_209993,RMVar_hsa_circ_327066,RMVar_hsa_circ_371408,RMVar_hsa_circ_284913,RMVar_hsa_circ_87434,RMVar_hsa_circ_124005,RMVar_hsa_circ_81656,RMVar_hsa_circ_92579,RMVar_hsa_circ_209999,RMVar_hsa_circ_12184,RMVar_hsa_circ_210001,RMVar_hsa_circ_210002,RMVar_hsa_circ_210000,RMVar_hsa_circ_209998,RMVar_hsa_circ_210004,RMVar_hsa_circ_92972,RMVar_hsa_circ_115210,RMVar_hsa_circ_124119,RMVar_hsa_circ_324320,RMVar_hsa_circ_210003,RMVar_hsa_circ_120583,RMVar_hsa_circ_210008,RMVar_hsa_circ_210012,RMVar_hsa_circ_88477,RMVar_hsa_circ_91985,RMVar_hsa_circ_210014,RMVar_hsa_circ_76115,RMVar_hsa_circ_210013,RMVar_hsa_circ_210010,RMVar_hsa_circ_210011,RMVar_hsa_circ_210009,RMVar_hsa_circ_113989,RMVar_hsa_circ_210016 49712 RMVar_ID_49712 Human_SNP_ID_680243124 A-to-I Human chr20 + 37212358 37212358 37212358 TACCTGTAGTCCAGCTACTTGGAGGTTGAGGCAGGAAGATCATTTGAACCGAGGAGCTTAAGACC TACCTGTAGTCCAGCTACTTGGAGGTTGAGGCGGGAAGATCATTTGAACCGAGGAGCTTAAGACC A G RPN2 Ensembl:ENSG00000118705 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202862869 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6997877,Human_RBP_ID_14095227 RMVar_hsa_circ_14258,RMVar_hsa_circ_209971,RMVar_hsa_circ_124357,RMVar_hsa_circ_95263,RMVar_hsa_circ_209972,RMVar_hsa_circ_123174,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_84350,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_317295,RMVar_hsa_circ_127936,RMVar_hsa_circ_84822,RMVar_hsa_circ_209991,RMVar_hsa_circ_105585,RMVar_hsa_circ_209987,RMVar_hsa_circ_209989,RMVar_hsa_circ_209990,RMVar_hsa_circ_209988,RMVar_hsa_circ_79324,RMVar_hsa_circ_83789,RMVar_hsa_circ_209992,RMVar_hsa_circ_209993,RMVar_hsa_circ_327066,RMVar_hsa_circ_371408,RMVar_hsa_circ_284913,RMVar_hsa_circ_87434,RMVar_hsa_circ_124005,RMVar_hsa_circ_81656,RMVar_hsa_circ_92579,RMVar_hsa_circ_209999,RMVar_hsa_circ_12184,RMVar_hsa_circ_210001,RMVar_hsa_circ_210002,RMVar_hsa_circ_210000,RMVar_hsa_circ_209998,RMVar_hsa_circ_210004,RMVar_hsa_circ_92972,RMVar_hsa_circ_115210,RMVar_hsa_circ_124119,RMVar_hsa_circ_324320,RMVar_hsa_circ_210003,RMVar_hsa_circ_120583,RMVar_hsa_circ_210008,RMVar_hsa_circ_210012,RMVar_hsa_circ_88477,RMVar_hsa_circ_91985,RMVar_hsa_circ_210014,RMVar_hsa_circ_76115,RMVar_hsa_circ_210013,RMVar_hsa_circ_210010,RMVar_hsa_circ_210011,RMVar_hsa_circ_210009,RMVar_hsa_circ_113989,RMVar_hsa_circ_210016 49713 RMVar_ID_49713 Human_SNP_ID_680243389 A-to-I Human chr20 + 37213424 37213424 37213424 GGTGGATCACTTGATCTCAGGACCCTGTCTCTACAAAAAACTGCAAAATTATCTGGACGTGATGG GGTGGATCACTTGATCTCAGGACCCTGTCTCTGCAAAAAACTGCAAAATTATCTGGACGTGATGG A G RPN2 Ensembl:ENSG00000118705 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs112088664 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6997878 RMVar_hsa_circ_14258,RMVar_hsa_circ_209971,RMVar_hsa_circ_124357,RMVar_hsa_circ_95263,RMVar_hsa_circ_209972,RMVar_hsa_circ_123174,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_84350,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_317295,RMVar_hsa_circ_127936,RMVar_hsa_circ_84822,RMVar_hsa_circ_209991,RMVar_hsa_circ_105585,RMVar_hsa_circ_209987,RMVar_hsa_circ_209989,RMVar_hsa_circ_209990,RMVar_hsa_circ_209988,RMVar_hsa_circ_79324,RMVar_hsa_circ_83789,RMVar_hsa_circ_209992,RMVar_hsa_circ_209993,RMVar_hsa_circ_327066,RMVar_hsa_circ_371408,RMVar_hsa_circ_284913,RMVar_hsa_circ_87434,RMVar_hsa_circ_124005,RMVar_hsa_circ_81656,RMVar_hsa_circ_92579,RMVar_hsa_circ_209999,RMVar_hsa_circ_12184,RMVar_hsa_circ_210001,RMVar_hsa_circ_210002,RMVar_hsa_circ_210000,RMVar_hsa_circ_209998,RMVar_hsa_circ_210004,RMVar_hsa_circ_92972,RMVar_hsa_circ_115210,RMVar_hsa_circ_124119,RMVar_hsa_circ_324320,RMVar_hsa_circ_210003,RMVar_hsa_circ_120583,RMVar_hsa_circ_210008,RMVar_hsa_circ_210012,RMVar_hsa_circ_88477,RMVar_hsa_circ_91985,RMVar_hsa_circ_210014,RMVar_hsa_circ_76115,RMVar_hsa_circ_210013,RMVar_hsa_circ_210010,RMVar_hsa_circ_210011,RMVar_hsa_circ_210009,RMVar_hsa_circ_113989,RMVar_hsa_circ_210016 49714 RMVar_ID_49714 Human_SNP_ID_680244615 A-to-I Human chr20 + 37218306 37218305 37218306 TGTATGGTGGCATGTACCTGTCCCAGCTACTTAAGAGGCTGAGGCAAGCGGATCCCTTGAGCCCA TGTATGGTGGCATGTACCTGTCCCAGCTACTT_AGAGGCTGAGGCAAGCGGATCCCTTGAGCCCA TA T RPN2 Ensembl:ENSG00000118705 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1214912706 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_209971,RMVar_hsa_circ_124357,RMVar_hsa_circ_95263,RMVar_hsa_circ_209972,RMVar_hsa_circ_123174,RMVar_hsa_circ_347488,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_84350,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_317295,RMVar_hsa_circ_127936,RMVar_hsa_circ_84822,RMVar_hsa_circ_209991,RMVar_hsa_circ_105585,RMVar_hsa_circ_209989,RMVar_hsa_circ_209990,RMVar_hsa_circ_209988,RMVar_hsa_circ_79324,RMVar_hsa_circ_83789,RMVar_hsa_circ_209992,RMVar_hsa_circ_209993,RMVar_hsa_circ_327066,RMVar_hsa_circ_371408,RMVar_hsa_circ_87434,RMVar_hsa_circ_124005,RMVar_hsa_circ_81656,RMVar_hsa_circ_92579,RMVar_hsa_circ_209999,RMVar_hsa_circ_12184,RMVar_hsa_circ_210001,RMVar_hsa_circ_210002,RMVar_hsa_circ_210000,RMVar_hsa_circ_210004,RMVar_hsa_circ_92972,RMVar_hsa_circ_115210,RMVar_hsa_circ_124119,RMVar_hsa_circ_210003,RMVar_hsa_circ_120583,RMVar_hsa_circ_210012,RMVar_hsa_circ_88477,RMVar_hsa_circ_91985,RMVar_hsa_circ_210014,RMVar_hsa_circ_76115,RMVar_hsa_circ_210013,RMVar_hsa_circ_210010,RMVar_hsa_circ_210011,RMVar_hsa_circ_210009,RMVar_hsa_circ_113989,RMVar_hsa_circ_210016,RMVar_hsa_circ_62417,RMVar_hsa_circ_293404,RMVar_hsa_circ_210017 49715 RMVar_ID_49715 Human_SNP_ID_680284071 A-to-I Human chr20 + 37380047 37380047 37380047 AGATGCTCTGAACACACTAACACATAAAGTGAAAAGAGGGAGGCGGCAGTGTAGAATCTCCTCTG AGATGCTCTGAACACACTAACACATAAAGTGAGAAGAGGGAGGCGGCAGTGTAGAATCTCCTCTG A G SRC Ensembl:ENSG00000197122 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041953409 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210031,RMVar_hsa_circ_369871 49716 RMVar_ID_49716 Human_SNP_ID_680313721 A-to-I Human chr20 - 37492140 37492140 37492140 TGGCTCAATGCAGCGTCGGACCTCCTAAGCTCAGGCAATCCTCCCACTTCAGCCTCCCAAGTGGC TGGCTCAATGCAGCGTCGGACCTCCTAAGCTCCGGCAATCCTCCCACTTCAGCCTCCCAAGTGGC T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs546837122 Functional Loss SNV dbSNP153 33..33 33 - - - 49717 RMVar_ID_49717 Human_SNP_ID_680317239 A-to-I Human chr20 - 37507988 37507988 37507988 ACAGTGGCTAATGCTTGTAATCTCAGCAGTTTAGGAGGCCAAGGCAGGAGGATTGCTTGAGCTTA ACAGTGGCTAATGCTTGTAATCTCAGCAGTTTGGGAGGCCAAGGCAGGAGGATTGCTTGAGCTTA T C BLCAP Ensembl:ENSG00000166619 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs964340654 Functional Loss SNV dbSNP153 33..33 33 - - - 49718 RMVar_ID_49718 Human_SNP_ID_680319898 A-to-I Human chr20 - 37519161 37519161 37519161 GCCCTGCCCGGCAGAGATCATGTATTGCCTCCAGTGGCTGCTGCCCGTCCTCCTCATCCCCAAGC GCCCTGCCCGGCAGAGATCATGTATTGCCTCCTGTGGCTGCTGCCCGTCCTCCTCATCCCCAAGC T A BLCAP Ensembl:ENSG00000166619 Protein coding intron GSE100210;GSE107867;GSE107867;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank;ASD brains,temporal_cortex;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,30559470,30559470,32596459 RNA-Seq:(High) rs1568682027 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_563609,Human_RBP_ID_4645973,Human_RBP_ID_17086027 Human_miRNA_ID_2476839,Human_miRNA_ID_2962621 RMVar_hsa_circ_112239,RMVar_hsa_circ_210041 49719 RMVar_ID_49719 Human_SNP_ID_680319904 A-to-I Human chr20 - 37519170 37519170 37519170 TTGGTGAAGGCCCTGCCCGGCAGAGATCATGTATTGCCTCCAGTGGCTGCTGCCCGTCCTCCTCA TTGGTGAAGGCCCTGCCCGGCAGAGATCATGTGTTGCCTCCAGTGGCTGCTGCCCGTCCTCCTCA T C BLCAP Ensembl:ENSG00000166619 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs11557677 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4645973,Human_RBP_ID_17086027 Human_miRNA_ID_2476839,Human_miRNA_ID_2962621 RMVar_hsa_circ_112239,RMVar_hsa_circ_210041 49720 RMVar_ID_49720 Human_SNP_ID_680371950 A-to-I Human chr20 + 37730748 37730748 37730748 CCTGTAGTCTCAGCTATTCAGAGGGCTGAGGCAGGAGGATTGCTGGAGCCCAGAAGTTCAGGTCC CCTGTAGTCTCAGCTATTCAGAGGGCTGAGGCCGGAGGATTGCTGGAGCCCAGAAGTTCAGGTCC A C CTNNBL1 Ensembl:ENSG00000132792 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1218145907 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69574 49721 RMVar_ID_49721 Human_SNP_ID_680371951 A-to-I Human chr20 + 37730748 37730748 37730748 CCTGTAGTCTCAGCTATTCAGAGGGCTGAGGCAGGAGGATTGCTGGAGCCCAGAAGTTCAGGTCC CCTGTAGTCTCAGCTATTCAGAGGGCTGAGGCGGGAGGATTGCTGGAGCCCAGAAGTTCAGGTCC A G CTNNBL1 Ensembl:ENSG00000132792 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1218145907 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69574 49722 RMVar_ID_49722 Human_SNP_ID_680396693 A-to-I Human chr20 + 37844441 37844441 37844441 AACAACGTTTGGTAACTCTGCCATTTTTGGACAATGGAATGAATTAAAAGCGCAGTGATAGGTTG AACAACGTTTGGTAACTCTGCCATTTTTGGACGATGGAATGAATTAAAAGCGCAGTGATAGGTTG A G CTNNBL1 Ensembl:ENSG00000132792 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs150259041 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210047,RMVar_hsa_circ_117586,RMVar_hsa_circ_360996,RMVar_hsa_circ_85226,RMVar_hsa_circ_210053,RMVar_hsa_circ_90948,RMVar_hsa_circ_210055,RMVar_hsa_circ_83850,RMVar_hsa_circ_3093,RMVar_hsa_circ_88667,RMVar_hsa_circ_210058,RMVar_hsa_circ_94332,RMVar_hsa_circ_210059,RMVar_hsa_circ_304672,RMVar_hsa_circ_210060 49723 RMVar_ID_49723 Human_SNP_ID_680399997 A-to-I Human chr20 + 37858799 37858799 37858799 CTGGATATGAGGACAGCAAGTCTGAGAGGTCTAGGGTTACAAAGGAGACTCCTGTGACTTAATTA CTGGATATGAGGACAGCAAGTCTGAGAGGTCTGGGGTTACAAAGGAGACTCCTGTGACTTAATTA A G CTNNBL1 Ensembl:ENSG00000132792 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs372494811 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210047,RMVar_hsa_circ_117586,RMVar_hsa_circ_360996,RMVar_hsa_circ_85226,RMVar_hsa_circ_210053,RMVar_hsa_circ_90948,RMVar_hsa_circ_210055,RMVar_hsa_circ_83850,RMVar_hsa_circ_3093,RMVar_hsa_circ_88667,RMVar_hsa_circ_210058,RMVar_hsa_circ_94332,RMVar_hsa_circ_210059,RMVar_hsa_circ_304672,RMVar_hsa_circ_210060 49724 RMVar_ID_49724 Human_SNP_ID_680435831 A-to-I Human chr20 - 38003023 38003023 38003023 CCATAAGTTTGAGATTGCAGTGAGCCGTGTTCACACCACTGTACTCCAGCTTGGACAGAGCAAGG CCATAAGTTTGAGATTGCAGTGAGCCGTGTTCGCACCACTGTACTCCAGCTTGGACAGAGCAAGG T C TTI1 Ensembl:ENSG00000101407 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1263711470 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14098222 RMVar_hsa_circ_34467,RMVar_hsa_circ_96729,RMVar_hsa_circ_103702,RMVar_hsa_circ_106881,RMVar_hsa_circ_210064,RMVar_hsa_circ_360909,RMVar_hsa_circ_210063,RMVar_hsa_circ_330060,RMVar_hsa_circ_77502,RMVar_hsa_circ_210070,RMVar_hsa_circ_210071,RMVar_hsa_circ_51311,RMVar_hsa_circ_210072 49725 RMVar_ID_49725 Human_SNP_ID_680436000 A-to-I Human chr20 - 38003713 38003713 38003713 AGTTTTGCTGTTGTTGCCCAGGCTGGAGTGCAATGGCACGATCTCGGCTCATTGCAACCTCTGCC AGTTTTGCTGTTGTTGCCCAGGCTGGAGTGCAGTGGCACGATCTCGGCTCATTGCAACCTCTGCC T C TTI1 Ensembl:ENSG00000101407 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1485755424 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34467,RMVar_hsa_circ_96729,RMVar_hsa_circ_103702,RMVar_hsa_circ_106881,RMVar_hsa_circ_210064,RMVar_hsa_circ_360909,RMVar_hsa_circ_210063,RMVar_hsa_circ_330060,RMVar_hsa_circ_77502,RMVar_hsa_circ_210070,RMVar_hsa_circ_210071,RMVar_hsa_circ_51311,RMVar_hsa_circ_210072 49726 RMVar_ID_49726 Human_SNP_ID_680454282 A-to-I Human chr20 + 38077161 38077161 38077161 GCGAGTCTTGAACTCATGACCTCAGGAGATCCACCCGCCTCAGCCTCCCAAAGCGCTGGGATTAC GCGAGTCTTGAACTCATGACCTCAGGAGATCCCCCCGCCTCAGCCTCCCAAAGCGCTGGGATTAC A C RPRD1B Ensembl:ENSG00000101413 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs998532913 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265836 49727 RMVar_ID_49727 Human_SNP_ID_680454288 A-to-I Human chr20 + 38077170 38077169 38077170 GAACTCATGACCTCAGGAGATCCACCCGCCTCAGCCTCCCAAAGCGCTGGGATTACAGACATGAG GAACTCATGACCTCAGGAGATCCACCCGCCTC_GCCTCCCAAAGCGCTGGGATTACAGACATGAG CA C RPRD1B Ensembl:ENSG00000101413 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1180904511 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_265836 49728 RMVar_ID_49728 Human_SNP_ID_680454289 A-to-I Human chr20 + 38077170 38077170 38077170 GAACTCATGACCTCAGGAGATCCACCCGCCTCAGCCTCCCAAAGCGCTGGGATTACAGACATGAG GAACTCATGACCTCAGGAGATCCACCCGCCTCGGCCTCCCAAAGCGCTGGGATTACAGACATGAG A G RPRD1B Ensembl:ENSG00000101413 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1460582740 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265836 49729 RMVar_ID_49729 Human_SNP_ID_680454489 A-to-I Human chr20 + 38078015 38078015 38078015 CTGAGCTACATGGCAAAACCCCGTCTCTATCAAAAATTAAAAAATTAGCTGGGCATCGTGGTTCA CTGAGCTACATGGCAAAACCCCGTCTCTATCAGAAATTAAAAAATTAGCTGGGCATCGTGGTTCA A G RPRD1B Ensembl:ENSG00000101413 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs534678671 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14100172 RMVar_hsa_circ_265836 49730 RMVar_ID_49730 Human_SNP_ID_680541186 A-to-I Human chr20 - 38412706 38412706 38412706 GTTGGCCAGGCTGGTCATGAACTTCTGGCCTCAAGTGATCTGCCTGCCTCGGCCTCGCAGAGTGC GTTGGCCAGGCTGGTCATGAACTTCTGGCCTCGAGTGATCTGCCTGCCTCGGCCTCGCAGAGTGC T C AL391095.2 Ensembl:ENSG00000224635 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1278161217 Functional Loss SNV dbSNP153 33..33 33 - - - 49731 RMVar_ID_49731 Human_SNP_ID_680542957 A-to-I Human chr20 - 38419996 38419996 38419996 TGCAAGGCCTAGGCATGGTGCCTTGTGCCTGTATTACTAGCACTTTGGGAGGCCAAGGTGGGATG TGCAAGGCCTAGGCATGGTGCCTTGTGCCTGTTTTACTAGCACTTTGGGAGGCCAAGGTGGGATG T A SNHG17 Ensembl:ENSG00000196756 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs950314068 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14101602,Human_RBP_ID_22817442 49732 RMVar_ID_49732 Human_SNP_ID_680546261 A-to-I Human chr20 - 38433040 38433040 38433040 TGAACCTGGGAGGTGGAGGTTGCAGTGAGCCAAGATCATGCCCCTGCACTCCAGCCTAGGCGACA TGAACCTGGGAGGTGGAGGTTGCAGTGAGCCAGGATCATGCCCCTGCACTCCAGCCTAGGCGACA T C SNHG17 Ensembl:ENSG00000196756 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1165463052 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571884 49733 RMVar_ID_49733 Human_SNP_ID_680546310 A-to-I Human chr20 - 38433264 38433264 38433264 ACAAATGAAAAACAGGAGATGGGCCGGGTGCAATGGCTCACACCTGTAATCCCAGCACTCTGAGA ACAAATGAAAAACAGGAGATGGGCCGGGTGCAGTGGCTCACACCTGTAATCCCAGCACTCTGAGA T C SNHG17 Ensembl:ENSG00000196756 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1313091381 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17571612 49734 RMVar_ID_49734 Human_SNP_ID_680546339 A-to-I Human chr20 - 38433403 38433401 38433403 CTGGCTTCAAGTGATTTTCCCTCAGTCTTCCAAAGTGCTGGAATTACAGGTGTGAGCCACTTCGC CTGGCTTCAAGTGATTTTCCCTCAGTCTTCCA__GTGCTGGAATTACAGGTGTGAGCCACTTCGC CTT C SNHG17 Ensembl:ENSG00000196756 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs576169249 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_17571613 49735 RMVar_ID_49735 Human_SNP_ID_680546375 A-to-I Human chr20 - 38433514 38433514 38433514 TGGCGTGATCATAGCTTGAACTCCTGTACTCAAGTGATCCTCGCACCTCAGCCTCCCAAATAGCT TGGCGTGATCATAGCTTGAACTCCTGTACTCAGGTGATCCTCGCACCTCAGCCTCCCAAATAGCT T C SNHG17 Ensembl:ENSG00000196756 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1032030273 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5249568,Human_RBP_ID_8260600,Human_RBP_ID_17571887 49736 RMVar_ID_49736 Human_SNP_ID_680546376 A-to-I Human chr20 - 38433514 38433514 38433514 TGGCGTGATCATAGCTTGAACTCCTGTACTCAAGTGATCCTCGCACCTCAGCCTCCCAAATAGCT TGGCGTGATCATAGCTTGAACTCCTGTACTCACGTGATCCTCGCACCTCAGCCTCCCAAATAGCT T G SNHG17 Ensembl:ENSG00000196756 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1032030273 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5249568,Human_RBP_ID_8260600,Human_RBP_ID_17571887 49737 RMVar_ID_49737 Human_SNP_ID_680571546 A-to-I Human chr20 + 38528871 38528871 38528871 CCCAGCTAATTTTTGTATTTTTTAGTAGACACAGGATTTTACCATGTTGGCCAAGCTGGTCTTGA CCCAGCTAATTTTTGTATTTTTTAGTAGACACCGGATTTTACCATGTTGGCCAAGCTGGTCTTGA A C RALGAPB Ensembl:ENSG00000170471 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1296963363 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14103180 RMVar_hsa_circ_18447,RMVar_hsa_circ_210089,RMVar_hsa_circ_83005,RMVar_hsa_circ_324912,RMVar_hsa_circ_51847,RMVar_hsa_circ_109189,RMVar_hsa_circ_210095,RMVar_hsa_circ_368052,RMVar_hsa_circ_288642,RMVar_hsa_circ_328368,RMVar_hsa_circ_210101,RMVar_hsa_circ_210100,RMVar_hsa_circ_47095,RMVar_hsa_circ_210102,RMVar_hsa_circ_368643,RMVar_hsa_circ_84636,RMVar_hsa_circ_42623,RMVar_hsa_circ_210109,RMVar_hsa_circ_210106,RMVar_hsa_circ_303655,RMVar_hsa_circ_210103,RMVar_hsa_circ_323516,RMVar_hsa_circ_323775,RMVar_hsa_circ_36263,RMVar_hsa_circ_45054,RMVar_hsa_circ_210108,RMVar_hsa_circ_210107,RMVar_hsa_circ_1189,RMVar_hsa_circ_314892,RMVar_hsa_circ_210110 49738 RMVar_ID_49738 Human_SNP_ID_680571547 A-to-I Human chr20 + 38528871 38528871 38528871 CCCAGCTAATTTTTGTATTTTTTAGTAGACACAGGATTTTACCATGTTGGCCAAGCTGGTCTTGA CCCAGCTAATTTTTGTATTTTTTAGTAGACACGGGATTTTACCATGTTGGCCAAGCTGGTCTTGA A G RALGAPB Ensembl:ENSG00000170471 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1296963363 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14103180 RMVar_hsa_circ_18447,RMVar_hsa_circ_210089,RMVar_hsa_circ_83005,RMVar_hsa_circ_324912,RMVar_hsa_circ_51847,RMVar_hsa_circ_109189,RMVar_hsa_circ_210095,RMVar_hsa_circ_368052,RMVar_hsa_circ_288642,RMVar_hsa_circ_328368,RMVar_hsa_circ_210101,RMVar_hsa_circ_210100,RMVar_hsa_circ_47095,RMVar_hsa_circ_210102,RMVar_hsa_circ_368643,RMVar_hsa_circ_84636,RMVar_hsa_circ_42623,RMVar_hsa_circ_210109,RMVar_hsa_circ_210106,RMVar_hsa_circ_303655,RMVar_hsa_circ_210103,RMVar_hsa_circ_323516,RMVar_hsa_circ_323775,RMVar_hsa_circ_36263,RMVar_hsa_circ_45054,RMVar_hsa_circ_210108,RMVar_hsa_circ_210107,RMVar_hsa_circ_1189,RMVar_hsa_circ_314892,RMVar_hsa_circ_210110 49739 RMVar_ID_49739 Human_SNP_ID_680634849 A-to-I Human chr20 + 38781477 38781477 38781477 CTCTTTCTTTCTTTTTTTTTTTTTTGAGACGCAGTCTGGCTCTGTCATCCAGGGTGGAGTGCAAT CTCTTTCTTTCTTTTTTTTTTTTTTGAGACGCCGTCTGGCTCTGTCATCCAGGGTGGAGTGCAAT A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170812722 Functional Loss SNV dbSNP153 33..33 33 - - - 49740 RMVar_ID_49740 Human_SNP_ID_680654559 A-to-I Human chr20 + 38865551 38865551 38865551 TGACCTTTGTGATCCGCCTGCCTCGGCCTCCTAAAGCACTGGGATTACAGGCGTGAGCCGCCGCG TGACCTTTGTGATCCGCCTGCCTCGGCCTCCTGAAGCACTGGGATTACAGGCGTGAGCCGCCGCG A G PPP1R16B Ensembl:ENSG00000101445 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1249779775 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94077,RMVar_hsa_circ_121138,RMVar_hsa_circ_98445,RMVar_hsa_circ_89388,RMVar_hsa_circ_210124,RMVar_hsa_circ_210125,RMVar_hsa_circ_210123,RMVar_hsa_circ_210127 49741 RMVar_ID_49741 Human_SNP_ID_680662992 A-to-I Human chr20 + 38899914 38899914 38899914 TGCCTCCCAGTTTCAAGCAATTCTCATGCCTCAGCCTCCCGAATAGCTGGGATTATAGGCTCCCA TGCCTCCCAGTTTCAAGCAATTCTCATGCCTCGGCCTCCCGAATAGCTGGGATTATAGGCTCCCA A G PPP1R16B Ensembl:ENSG00000101445 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1268128105 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94077,RMVar_hsa_circ_98445,RMVar_hsa_circ_210124,RMVar_hsa_circ_210125,RMVar_hsa_circ_37294,RMVar_hsa_circ_105371,RMVar_hsa_circ_19193,RMVar_hsa_circ_210129,RMVar_hsa_circ_51990,RMVar_hsa_circ_210128,RMVar_hsa_circ_99711 49742 RMVar_ID_49742 Human_SNP_ID_680665684 A-to-I Human chr20 + 38910646 38910646 38910646 GCCTTGACCTCTTGGGATCAAGCGATCCTCCCACCTCAGCCTCTTGGGTAGCTGGGACTATAGGC GCCTTGACCTCTTGGGATCAAGCGATCCTCCCTCCTCAGCCTCTTGGGTAGCTGGGACTATAGGC A T PPP1R16B Ensembl:ENSG00000101445 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1470110842 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98445,RMVar_hsa_circ_210125 49743 RMVar_ID_49743 Human_SNP_ID_680666772 A-to-I Human chr20 + 38914868 38914868 38914868 TTTAAATATTTGGGTAGTGATGAGGTCTCACTATGTTGCCCAGGCTGGTCTCCAACTCTTAGGCT TTTAAATATTTGGGTAGTGATGAGGTCTCACTGTGTTGCCCAGGCTGGTCTCCAACTCTTAGGCT A G PPP1R16B Ensembl:ENSG00000101445 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1228629875 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98445,RMVar_hsa_circ_210125 49744 RMVar_ID_49744 Human_SNP_ID_680666935 A-to-I Human chr20 + 38915618 38915618 38915618 ACAATTATCCTGCCTCAGCCTCCTGAGTAGCTAGGATTAGAGGCCTGCGTCACTGCGCCTGTCTA ACAATTATCCTGCCTCAGCCTCCTGAGTAGCTGGGATTAGAGGCCTGCGTCACTGCGCCTGTCTA A G PPP1R16B Ensembl:ENSG00000101445 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs943113586 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98445,RMVar_hsa_circ_210125 49745 RMVar_ID_49745 Human_SNP_ID_680671575 A-to-I Human chr20 + 38933924 38933924 38933924 GTCGCCAGGCTGGAGTGCAGTGGCACCATCTCAGCTCACTGCAACTTCTGCCTCCCGGGTTCAAG GTCGCCAGGCTGGAGTGCAGTGGCACCATCTCGGCTCACTGCAACTTCTGCCTCCCGGGTTCAAG A G FAM83D Ensembl:ENSG00000101447 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1162279241 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_210137,RMVar_hsa_circ_123444 49746 RMVar_ID_49746 Human_SNP_ID_680673658 A-to-I Human chr20 + 38943078 38943078 38943078 ATAGAGTCTCACTCTGTTGCCCAGGCTGGAGTACAGTGGCCCAATCTAGGCTCACTGCAACATCC ATAGAGTCTCACTCTGTTGCCCAGGCTGGAGTGCAGTGGCCCAATCTAGGCTCACTGCAACATCC A G FAM83D Ensembl:ENSG00000101447 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs973741957 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25611368 RMVar_hsa_circ_94366,RMVar_hsa_circ_210137,RMVar_hsa_circ_123444,RMVar_hsa_circ_273310,RMVar_hsa_circ_210138,RMVar_hsa_circ_210139 49747 RMVar_ID_49747 Human_SNP_ID_680674023 A-to-I Human chr20 + 38944776 38944776 38944776 CCTGGCTAACACGGTGAAACCGCGTCTCTACTAAAAATATAAAAAATTAGCCAGGCCTGGTGGCA CCTGGCTAACACGGTGAAACCGCGTCTCTACTGAAAATATAAAAAATTAGCCAGGCCTGGTGGCA A G FAM83D Ensembl:ENSG00000101447 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1400369580 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94366,RMVar_hsa_circ_210137,RMVar_hsa_circ_123444,RMVar_hsa_circ_273310,RMVar_hsa_circ_210138,RMVar_hsa_circ_210139 49748 RMVar_ID_49748 Human_SNP_ID_680674036 A-to-I Human chr20 + 38944844 38944844 38944844 GCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGAAGGAGAATCGCTTGAACCCGGGAGGCAGAGGT GCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGGGAGGCAGAGGT A C FAM83D Ensembl:ENSG00000101447 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs62204119 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_6133,GWAS_ID_6134,GWAS_ID_6135,GWAS_ID_6136,GWAS_ID_6137,GWAS_ID_6138,GWAS_ID_6139,GWAS_ID_6140,GWAS_ID_6141,GWAS_ID_6142,GWAS_ID_6143,GWAS_ID_6144,GWAS_ID_6145,GWAS_ID_6146,GWAS_ID_6147,GWAS_ID_6148,GWAS_ID_6149,GWAS_ID_6150 RMVar_hsa_circ_94366,RMVar_hsa_circ_210137,RMVar_hsa_circ_123444,RMVar_hsa_circ_273310,RMVar_hsa_circ_210138,RMVar_hsa_circ_210139 49749 RMVar_ID_49749 Human_SNP_ID_680675547 A-to-I Human chr20 + 38951097 38951097 38951097 TGCCCACTTCATCCTCTCAAAGTGCTGGGATTACAGTCATGAGCCACCGCGCCTGGCCCCCTTTC TGCCCACTTCATCCTCTCAAAGTGCTGGGATTCCAGTCATGAGCCACCGCGCCTGGCCCCCTTTC A C FAM83D Ensembl:ENSG00000101447 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1018663738 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94366,RMVar_hsa_circ_210139 49750 RMVar_ID_49750 Human_SNP_ID_282872323 A-to-I Human chr6 - 75188393 75188393 75188393 ATCATCTCCCAGGTGTGCTCAGGTGTTGATGAACAACTTGGTGAATTGGTTAGTGGAGAAGAAGG ATCATCTCCCAGGTGTGCTCAGGTGTTGATGAGCAACTTGGTGAATTGGTTAGTGGAGAAGAAGG T C COL12A1 Ensembl:ENSG00000111799 Protein coding 5'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1298395483 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_787193,Human_Splice_Rec_787325,Human_Splice_Rec_787549,Human_Splice_Rec_787673,Human_Splice_Rec_787837 Human_miRNA_ID_1543561,Human_miRNA_ID_1596482,Human_miRNA_ID_2566566 RMVar_hsa_circ_117407,RMVar_hsa_circ_239568,RMVar_hsa_circ_19342,RMVar_hsa_circ_86966,RMVar_hsa_circ_239591,RMVar_hsa_circ_239598,RMVar_hsa_circ_115541,RMVar_hsa_circ_50540,RMVar_hsa_circ_116981,RMVar_hsa_circ_239603,RMVar_hsa_circ_125381,RMVar_hsa_circ_346771,RMVar_hsa_circ_375514,RMVar_hsa_circ_239605,RMVar_hsa_circ_50813,RMVar_hsa_circ_127336,RMVar_hsa_circ_239607,RMVar_hsa_circ_239610,RMVar_hsa_circ_114289,RMVar_hsa_circ_239611,RMVar_hsa_circ_239609,RMVar_hsa_circ_49506,RMVar_hsa_circ_38975,RMVar_hsa_circ_304004,RMVar_hsa_circ_104728,RMVar_hsa_circ_239614 49751 RMVar_ID_49751 Human_SNP_ID_282884385 A-to-I Human chr6 - 75238922 75238922 75238922 CAATCCCAGCTACTCGTGAAGCTGAGGCAGGAAGATTGCTTGAACTGGTAGGCGGAGGTTGCAGT CAATCCCAGCTACTCGTGAAGCTGAGGCAGGAGGATTGCTTGAACTGGTAGGCGGAGGTTGCAGT T C COX7A2 Ensembl:ENSG00000112695 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1201417006 Functional Loss SNV dbSNP153 33..33 33 - - - 49752 RMVar_ID_49752 Human_SNP_ID_282884393 A-to-I Human chr6 - 75238952 75238952 75238952 AAATGAGTCGGGTGTGATGGCACACACTTGCAATCCCAGCTACTCGTGAAGCTGAGGCAGGAAGA AAATGAGTCGGGTGTGATGGCACACACTTGCAGTCCCAGCTACTCGTGAAGCTGAGGCAGGAAGA T C COX7A2 Ensembl:ENSG00000112695 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs909595506 Functional Loss SNV dbSNP153 33..33 33 - - - 49753 RMVar_ID_49753 Human_SNP_ID_282884400 A-to-I Human chr6 - 75238979 75238979 75238979 GAAACCCTGTCTGTACTAAAAACACAAAAATGAGTCGGGTGTGATGGCACACACTTGCAATCCCA GAAACCCTGTCTGTACTAAAAACACAAAAATGGGTCGGGTGTGATGGCACACACTTGCAATCCCA T C COX7A2 Ensembl:ENSG00000112695 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1413936923 Functional Loss SNV dbSNP153 33..33 33 - - - 49754 RMVar_ID_49754 Human_SNP_ID_282884402 A-to-I Human chr6 - 75238988 75238988 75238988 ACACATGGTGAAACCCTGTCTGTACTAAAAACACAAAAATGAGTCGGGTGTGATGGCACACACTT ACACATGGTGAAACCCTGTCTGTACTAAAAACGCAAAAATGAGTCGGGTGTGATGGCACACACTT T C COX7A2 Ensembl:ENSG00000112695 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1193407663 Functional Loss SNV dbSNP153 33..33 33 - - - 49755 RMVar_ID_49755 Human_SNP_ID_282884403 A-to-I Human chr6 - 75238991 75238989 75238992 GGCACACATGGTGAAACCCTGTCTGTACTAAAAACACAAAAATGAGTCGGGTGTGATGGCACACA GGCACACATGGTGAAACCCTGTCTGTACTAA___CACAAAAATGAGTCGGGTGTGATGGCACACA GTTT G COX7A2 Ensembl:ENSG00000112695 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474654828 Functional Loss DEL dbSNP153 32..34 33 - - - 49756 RMVar_ID_49756 Human_SNP_ID_282895709 A-to-I Human chr6 + 75288514 75288514 75288514 CACCTCCCAGGCTCAAGCGATTCTCCAACCTCAGCCTCCCAAGTACGTGGGACCACAGGTGCGTG CACCTCCCAGGCTCAAGCGATTCTCCAACCTCGGCCTCCCAAGTACGTGGGACCACAGGTGCGTG A G AL080250.1 Ensembl:ENSG00000225793 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232462254 Functional Loss SNV dbSNP153 33..33 33 - - - 49757 RMVar_ID_49757 Human_SNP_ID_282969387 A-to-I Human chr6 + 75612540 75612540 75612540 TTTTGTAGAGACAGAGTGTCACTATGCTGCTCAGGCTGCTCTCGACTTCTGGCCTCAAGCAATCC TTTTGTAGAGACAGAGTGTCACTATGCTGCTCGGGCTGCTCTCGACTTCTGGCCTCAAGCAATCC A G SENP6 Ensembl:ENSG00000112701 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1473240694 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15878498 49758 RMVar_ID_49758 Human_SNP_ID_282969512 A-to-I Human chr6 + 75613003 75613003 75613003 GGGCATCGTGGCATATGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCACGAGAATCGCTTGAA GGGCATCGTGGCATATGCCTGTAATCCCAGCTCCTTGGGAGGCTGAGGCACGAGAATCGCTTGAA A C SENP6 Ensembl:ENSG00000112701 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334623883 Functional Loss SNV dbSNP153 33..33 33 - - - 49759 RMVar_ID_49759 Human_SNP_ID_282969513 A-to-I Human chr6 + 75613003 75613003 75613003 GGGCATCGTGGCATATGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCACGAGAATCGCTTGAA GGGCATCGTGGCATATGCCTGTAATCCCAGCTGCTTGGGAGGCTGAGGCACGAGAATCGCTTGAA A G SENP6 Ensembl:ENSG00000112701 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334623883 Functional Loss SNV dbSNP153 33..33 33 - - - 49760 RMVar_ID_49760 Human_SNP_ID_282972760 A-to-I Human chr6 + 75625597 75625597 75625597 GTTAATTTAATAACTTATTTGGGGCTGGGCACAGTGGCTTATGCCAGTAATCCCAACACTTTGGG GTTAATTTAATAACTTATTTGGGGCTGGGCACGGTGGCTTATGCCAGTAATCCCAACACTTTGGG A G SENP6 Ensembl:ENSG00000112701 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs892359900 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_251348,Human_RBP_ID_17576735 RMVar_hsa_circ_74039,RMVar_hsa_circ_354713,RMVar_hsa_circ_378836,RMVar_hsa_circ_302921,RMVar_hsa_circ_278822,RMVar_hsa_circ_281774,RMVar_hsa_circ_74233,RMVar_hsa_circ_239631,RMVar_hsa_circ_239632,RMVar_hsa_circ_239633,RMVar_hsa_circ_239630,RMVar_hsa_circ_239635,RMVar_hsa_circ_315505,RMVar_hsa_circ_239636,RMVar_hsa_circ_72736 49761 RMVar_ID_49761 Human_SNP_ID_282975483 A-to-I Human chr6 + 75637026 75637026 75637026 CTTCAGCCTCCTGAGTAACTAGGACTGCAGGCATGCACCACCGCACCAGGCTAACTTTAAAAAAA CTTCAGCCTCCTGAGTAACTAGGACTGCAGGCGTGCACCACCGCACCAGGCTAACTTTAAAAAAA A G SENP6 Ensembl:ENSG00000112701 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1165140735 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7628710,Human_RBP_ID_15879118 RMVar_hsa_circ_239641,RMVar_hsa_circ_72907,RMVar_hsa_circ_74039,RMVar_hsa_circ_378836,RMVar_hsa_circ_302921,RMVar_hsa_circ_281774,RMVar_hsa_circ_74233,RMVar_hsa_circ_239631,RMVar_hsa_circ_239632,RMVar_hsa_circ_239633,RMVar_hsa_circ_239636,RMVar_hsa_circ_312023,RMVar_hsa_circ_347478,RMVar_hsa_circ_372206,RMVar_hsa_circ_72736,RMVar_hsa_circ_360461,RMVar_hsa_circ_340498,RMVar_hsa_circ_274569,RMVar_hsa_circ_307977,RMVar_hsa_circ_239638,RMVar_hsa_circ_41861,RMVar_hsa_circ_239639,RMVar_hsa_circ_346240,RMVar_hsa_circ_325928,RMVar_hsa_circ_300774,RMVar_hsa_circ_304108,RMVar_hsa_circ_282772,RMVar_hsa_circ_7430,RMVar_hsa_circ_20892,RMVar_hsa_circ_270052,RMVar_hsa_circ_20628,RMVar_hsa_circ_239643,RMVar_hsa_circ_239645,RMVar_hsa_circ_239646,RMVar_hsa_circ_239644,RMVar_hsa_circ_239642,RMVar_hsa_circ_239640 49762 RMVar_ID_49762 Human_SNP_ID_282975723 A-to-I Human chr6 + 75638022 75638022 75638022 ATTACAGGCGTGTGCCACCATGCCCAGCTAATATTTGTGTGTGTGTGTTTTTAGTAGAGATGCGG ATTACAGGCGTGTGCCACCATGCCCAGCTAATGTTTGTGTGTGTGTGTTTTTAGTAGAGATGCGG A G SENP6 Ensembl:ENSG00000112701 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs911887485 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3814902,Human_RBP_ID_24171753 RMVar_hsa_circ_239641,RMVar_hsa_circ_72907,RMVar_hsa_circ_74039,RMVar_hsa_circ_378836,RMVar_hsa_circ_302921,RMVar_hsa_circ_281774,RMVar_hsa_circ_74233,RMVar_hsa_circ_239631,RMVar_hsa_circ_239632,RMVar_hsa_circ_239633,RMVar_hsa_circ_239636,RMVar_hsa_circ_312023,RMVar_hsa_circ_347478,RMVar_hsa_circ_372206,RMVar_hsa_circ_72736,RMVar_hsa_circ_360461,RMVar_hsa_circ_340498,RMVar_hsa_circ_274569,RMVar_hsa_circ_307977,RMVar_hsa_circ_239638,RMVar_hsa_circ_41861,RMVar_hsa_circ_239639,RMVar_hsa_circ_346240,RMVar_hsa_circ_325928,RMVar_hsa_circ_300774,RMVar_hsa_circ_304108,RMVar_hsa_circ_282772,RMVar_hsa_circ_7430,RMVar_hsa_circ_20892,RMVar_hsa_circ_270052,RMVar_hsa_circ_20628,RMVar_hsa_circ_239643,RMVar_hsa_circ_239645,RMVar_hsa_circ_239646,RMVar_hsa_circ_239644,RMVar_hsa_circ_239642,RMVar_hsa_circ_239640 49763 RMVar_ID_49763 Human_SNP_ID_282975724 A-to-I Human chr6 + 75638022 75638022 75638022 ATTACAGGCGTGTGCCACCATGCCCAGCTAATATTTGTGTGTGTGTGTTTTTAGTAGAGATGCGG ATTACAGGCGTGTGCCACCATGCCCAGCTAATTTTTGTGTGTGTGTGTTTTTAGTAGAGATGCGG A T SENP6 Ensembl:ENSG00000112701 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs911887485 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3814902,Human_RBP_ID_24171753 RMVar_hsa_circ_239641,RMVar_hsa_circ_72907,RMVar_hsa_circ_74039,RMVar_hsa_circ_378836,RMVar_hsa_circ_302921,RMVar_hsa_circ_281774,RMVar_hsa_circ_74233,RMVar_hsa_circ_239631,RMVar_hsa_circ_239632,RMVar_hsa_circ_239633,RMVar_hsa_circ_239636,RMVar_hsa_circ_312023,RMVar_hsa_circ_347478,RMVar_hsa_circ_372206,RMVar_hsa_circ_72736,RMVar_hsa_circ_360461,RMVar_hsa_circ_340498,RMVar_hsa_circ_274569,RMVar_hsa_circ_307977,RMVar_hsa_circ_239638,RMVar_hsa_circ_41861,RMVar_hsa_circ_239639,RMVar_hsa_circ_346240,RMVar_hsa_circ_325928,RMVar_hsa_circ_300774,RMVar_hsa_circ_304108,RMVar_hsa_circ_282772,RMVar_hsa_circ_7430,RMVar_hsa_circ_20892,RMVar_hsa_circ_270052,RMVar_hsa_circ_20628,RMVar_hsa_circ_239643,RMVar_hsa_circ_239645,RMVar_hsa_circ_239646,RMVar_hsa_circ_239644,RMVar_hsa_circ_239642,RMVar_hsa_circ_239640 49764 RMVar_ID_49764 Human_SNP_ID_282976190 A-to-I Human chr6 + 75638937 75638937 75638937 AACATTAGCCAGGCATAGTGGTGCACACTTGTAGTCCCAGCTGCTCAAGGTGGGAGAATCACCTG AACATTAGCCAGGCATAGTGGTGCACACTTGTGGTCCCAGCTGCTCAAGGTGGGAGAATCACCTG A G SENP6 Ensembl:ENSG00000112701 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs375775760 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7628760 RMVar_hsa_circ_239641,RMVar_hsa_circ_72907,RMVar_hsa_circ_74039,RMVar_hsa_circ_378836,RMVar_hsa_circ_302921,RMVar_hsa_circ_281774,RMVar_hsa_circ_74233,RMVar_hsa_circ_239631,RMVar_hsa_circ_239632,RMVar_hsa_circ_239633,RMVar_hsa_circ_239636,RMVar_hsa_circ_312023,RMVar_hsa_circ_347478,RMVar_hsa_circ_372206,RMVar_hsa_circ_72736,RMVar_hsa_circ_360461,RMVar_hsa_circ_340498,RMVar_hsa_circ_274569,RMVar_hsa_circ_307977,RMVar_hsa_circ_239638,RMVar_hsa_circ_41861,RMVar_hsa_circ_239639,RMVar_hsa_circ_346240,RMVar_hsa_circ_325928,RMVar_hsa_circ_300774,RMVar_hsa_circ_304108,RMVar_hsa_circ_282772,RMVar_hsa_circ_7430,RMVar_hsa_circ_20892,RMVar_hsa_circ_270052,RMVar_hsa_circ_20628,RMVar_hsa_circ_239643,RMVar_hsa_circ_239645,RMVar_hsa_circ_239646,RMVar_hsa_circ_239644,RMVar_hsa_circ_239642,RMVar_hsa_circ_239640 49765 RMVar_ID_49765 Human_SNP_ID_282976852 A-to-I Human chr6 + 75641745 75641745 75641745 CACACCTATAATCTTAGTACTTTGGGAGGGCAAAGCGGGAGTATCTCTTGAGCCCAGGAGTTCCA CACACCTATAATCTTAGTACTTTGGGAGGGCAGAGCGGGAGTATCTCTTGAGCCCAGGAGTTCCA A G SENP6 Ensembl:ENSG00000112701 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560056327 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7628827,Human_RBP_ID_15879341,Human_RBP_ID_18869293 RMVar_hsa_circ_239641,RMVar_hsa_circ_72907,RMVar_hsa_circ_74039,RMVar_hsa_circ_302921,RMVar_hsa_circ_281774,RMVar_hsa_circ_74233,RMVar_hsa_circ_239632,RMVar_hsa_circ_239633,RMVar_hsa_circ_239636,RMVar_hsa_circ_312023,RMVar_hsa_circ_347478,RMVar_hsa_circ_372206,RMVar_hsa_circ_72736,RMVar_hsa_circ_360461,RMVar_hsa_circ_274569,RMVar_hsa_circ_239638,RMVar_hsa_circ_41861,RMVar_hsa_circ_239639,RMVar_hsa_circ_346240,RMVar_hsa_circ_325928,RMVar_hsa_circ_300774,RMVar_hsa_circ_304108,RMVar_hsa_circ_282772,RMVar_hsa_circ_7430,RMVar_hsa_circ_20892,RMVar_hsa_circ_270052,RMVar_hsa_circ_20628,RMVar_hsa_circ_239643,RMVar_hsa_circ_239645,RMVar_hsa_circ_239644,RMVar_hsa_circ_239642,RMVar_hsa_circ_239640 49766 RMVar_ID_49766 Human_SNP_ID_282977252 A-to-I Human chr6 + 75643601 75643601 75643601 AAAATTAGCCGGGTGTGATGGCATGCGCCTGTAATCCCAGCTACTCGGGAGGTTGAGACATGAGA AAAATTAGCCGGGTGTGATGGCATGCGCCTGTGATCCCAGCTACTCGGGAGGTTGAGACATGAGA A G SENP6 Ensembl:ENSG00000112701 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs748986950 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_239641,RMVar_hsa_circ_72907,RMVar_hsa_circ_74039,RMVar_hsa_circ_302921,RMVar_hsa_circ_281774,RMVar_hsa_circ_74233,RMVar_hsa_circ_239632,RMVar_hsa_circ_239633,RMVar_hsa_circ_239636,RMVar_hsa_circ_312023,RMVar_hsa_circ_347478,RMVar_hsa_circ_372206,RMVar_hsa_circ_72736,RMVar_hsa_circ_360461,RMVar_hsa_circ_274569,RMVar_hsa_circ_239638,RMVar_hsa_circ_41861,RMVar_hsa_circ_239639,RMVar_hsa_circ_346240,RMVar_hsa_circ_325928,RMVar_hsa_circ_300774,RMVar_hsa_circ_304108,RMVar_hsa_circ_282772,RMVar_hsa_circ_7430,RMVar_hsa_circ_20892,RMVar_hsa_circ_270052,RMVar_hsa_circ_20628,RMVar_hsa_circ_239643,RMVar_hsa_circ_239645,RMVar_hsa_circ_239644,RMVar_hsa_circ_239642,RMVar_hsa_circ_239640 49767 RMVar_ID_49767 Human_SNP_ID_282977256 A-to-I Human chr6 + 75643611 75643611 75643611 GGGTGTGATGGCATGCGCCTGTAATCCCAGCTACTCGGGAGGTTGAGACATGAGAATTGCTTGAA GGGTGTGATGGCATGCGCCTGTAATCCCAGCTGCTCGGGAGGTTGAGACATGAGAATTGCTTGAA A G SENP6 Ensembl:ENSG00000112701 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs975612512 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_239641,RMVar_hsa_circ_72907,RMVar_hsa_circ_74039,RMVar_hsa_circ_302921,RMVar_hsa_circ_281774,RMVar_hsa_circ_74233,RMVar_hsa_circ_239632,RMVar_hsa_circ_239633,RMVar_hsa_circ_239636,RMVar_hsa_circ_312023,RMVar_hsa_circ_347478,RMVar_hsa_circ_372206,RMVar_hsa_circ_72736,RMVar_hsa_circ_360461,RMVar_hsa_circ_274569,RMVar_hsa_circ_239638,RMVar_hsa_circ_41861,RMVar_hsa_circ_239639,RMVar_hsa_circ_346240,RMVar_hsa_circ_325928,RMVar_hsa_circ_300774,RMVar_hsa_circ_304108,RMVar_hsa_circ_282772,RMVar_hsa_circ_7430,RMVar_hsa_circ_20892,RMVar_hsa_circ_270052,RMVar_hsa_circ_20628,RMVar_hsa_circ_239643,RMVar_hsa_circ_239645,RMVar_hsa_circ_239644,RMVar_hsa_circ_239642,RMVar_hsa_circ_239640 49768 RMVar_ID_49768 Human_SNP_ID_282977504 A-to-I Human chr6 + 75644506 75644504 75644506 TCTTTTTTTTTTTTTTGTTTTCTTTTTCTTTGAGACAGTCTGGCTCTGTCGCCTAGGCTAGAGGG TCTTTTTTTTTTTTTTGTTTTCTTTTTCTTT__GACAGTCTGGCTCTGTCGCCTAGGCTAGAGGG TGA T SENP6 Ensembl:ENSG00000112701 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223036272 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_3018146,Human_RBP_ID_7628863,Human_RBP_ID_15879444,Human_RBP_ID_24513304 RMVar_hsa_circ_239641,RMVar_hsa_circ_72907,RMVar_hsa_circ_74039,RMVar_hsa_circ_302921,RMVar_hsa_circ_281774,RMVar_hsa_circ_74233,RMVar_hsa_circ_239632,RMVar_hsa_circ_239633,RMVar_hsa_circ_239636,RMVar_hsa_circ_312023,RMVar_hsa_circ_347478,RMVar_hsa_circ_372206,RMVar_hsa_circ_72736,RMVar_hsa_circ_360461,RMVar_hsa_circ_274569,RMVar_hsa_circ_239638,RMVar_hsa_circ_41861,RMVar_hsa_circ_239639,RMVar_hsa_circ_346240,RMVar_hsa_circ_325928,RMVar_hsa_circ_300774,RMVar_hsa_circ_304108,RMVar_hsa_circ_282772,RMVar_hsa_circ_7430,RMVar_hsa_circ_20892,RMVar_hsa_circ_270052,RMVar_hsa_circ_20628,RMVar_hsa_circ_239643,RMVar_hsa_circ_239645,RMVar_hsa_circ_239644,RMVar_hsa_circ_239642,RMVar_hsa_circ_239640 49769 RMVar_ID_49769 Human_SNP_ID_282977510 A-to-I Human chr6 + 75644533 75644533 75644533 CTTTGAGACAGTCTGGCTCTGTCGCCTAGGCTAGAGGGCAATGGTGCAACCTTGGCTCACTGCAA CTTTGAGACAGTCTGGCTCTGTCGCCTAGGCTGGAGGGCAATGGTGCAACCTTGGCTCACTGCAA A G SENP6 Ensembl:ENSG00000112701 Protein coding intron GSE38233;GSE100210;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,temporal_cortex - 24183664,29129909,30559470 RNA-Seq:(High) rs1472582817 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7628863 RMVar_hsa_circ_239641,RMVar_hsa_circ_72907,RMVar_hsa_circ_74039,RMVar_hsa_circ_302921,RMVar_hsa_circ_281774,RMVar_hsa_circ_74233,RMVar_hsa_circ_239632,RMVar_hsa_circ_239633,RMVar_hsa_circ_239636,RMVar_hsa_circ_312023,RMVar_hsa_circ_347478,RMVar_hsa_circ_372206,RMVar_hsa_circ_72736,RMVar_hsa_circ_360461,RMVar_hsa_circ_274569,RMVar_hsa_circ_239638,RMVar_hsa_circ_41861,RMVar_hsa_circ_239639,RMVar_hsa_circ_346240,RMVar_hsa_circ_325928,RMVar_hsa_circ_300774,RMVar_hsa_circ_304108,RMVar_hsa_circ_282772,RMVar_hsa_circ_7430,RMVar_hsa_circ_20892,RMVar_hsa_circ_270052,RMVar_hsa_circ_20628,RMVar_hsa_circ_239643,RMVar_hsa_circ_239645,RMVar_hsa_circ_239644,RMVar_hsa_circ_239642,RMVar_hsa_circ_239640 49770 RMVar_ID_49770 Human_SNP_ID_282977514 A-to-I Human chr6 + 75644548 75644548 75644548 GCTCTGTCGCCTAGGCTAGAGGGCAATGGTGCAACCTTGGCTCACTGCAACCTCTGCCTCTCAGG GCTCTGTCGCCTAGGCTAGAGGGCAATGGTGCGACCTTGGCTCACTGCAACCTCTGCCTCTCAGG A G SENP6 Ensembl:ENSG00000112701 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs914787245 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_239641,RMVar_hsa_circ_72907,RMVar_hsa_circ_74039,RMVar_hsa_circ_302921,RMVar_hsa_circ_281774,RMVar_hsa_circ_74233,RMVar_hsa_circ_239632,RMVar_hsa_circ_239633,RMVar_hsa_circ_239636,RMVar_hsa_circ_312023,RMVar_hsa_circ_347478,RMVar_hsa_circ_372206,RMVar_hsa_circ_72736,RMVar_hsa_circ_360461,RMVar_hsa_circ_274569,RMVar_hsa_circ_239638,RMVar_hsa_circ_41861,RMVar_hsa_circ_239639,RMVar_hsa_circ_346240,RMVar_hsa_circ_325928,RMVar_hsa_circ_300774,RMVar_hsa_circ_304108,RMVar_hsa_circ_282772,RMVar_hsa_circ_7430,RMVar_hsa_circ_20892,RMVar_hsa_circ_270052,RMVar_hsa_circ_20628,RMVar_hsa_circ_239643,RMVar_hsa_circ_239645,RMVar_hsa_circ_239644,RMVar_hsa_circ_239642,RMVar_hsa_circ_239640 49771 RMVar_ID_49771 Human_SNP_ID_282977519 A-to-I Human chr6 + 75644559 75644559 75644559 TAGGCTAGAGGGCAATGGTGCAACCTTGGCTCACTGCAACCTCTGCCTCTCAGGTTCAAGCAATT TAGGCTAGAGGGCAATGGTGCAACCTTGGCTCCCTGCAACCTCTGCCTCTCAGGTTCAAGCAATT A C SENP6 Ensembl:ENSG00000112701 Protein coding intron GSE38233;GSE107867 cultured B-cells;ASD brains,frontal_cortex - 24183664,30559470 RNA-Seq:(High) rs567824584 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_239641,RMVar_hsa_circ_72907,RMVar_hsa_circ_74039,RMVar_hsa_circ_302921,RMVar_hsa_circ_281774,RMVar_hsa_circ_74233,RMVar_hsa_circ_239632,RMVar_hsa_circ_239633,RMVar_hsa_circ_239636,RMVar_hsa_circ_312023,RMVar_hsa_circ_347478,RMVar_hsa_circ_372206,RMVar_hsa_circ_72736,RMVar_hsa_circ_360461,RMVar_hsa_circ_274569,RMVar_hsa_circ_239638,RMVar_hsa_circ_41861,RMVar_hsa_circ_239639,RMVar_hsa_circ_346240,RMVar_hsa_circ_325928,RMVar_hsa_circ_300774,RMVar_hsa_circ_304108,RMVar_hsa_circ_282772,RMVar_hsa_circ_7430,RMVar_hsa_circ_20892,RMVar_hsa_circ_270052,RMVar_hsa_circ_20628,RMVar_hsa_circ_239643,RMVar_hsa_circ_239645,RMVar_hsa_circ_239644,RMVar_hsa_circ_239642,RMVar_hsa_circ_239640 49772 RMVar_ID_49772 Human_SNP_ID_282977540 A-to-I Human chr6 + 75644659 75644659 75644659 GGCATGTACCACCATGCCTGGCTGATTTTTGTATTTTTAGTAGAGACGGTGTTTCGCCATGTTGG GGCATGTACCACCATGCCTGGCTGATTTTTGTGTTTTTAGTAGAGACGGTGTTTCGCCATGTTGG A G SENP6 Ensembl:ENSG00000112701 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs899904319 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_239641,RMVar_hsa_circ_72907,RMVar_hsa_circ_74039,RMVar_hsa_circ_302921,RMVar_hsa_circ_281774,RMVar_hsa_circ_74233,RMVar_hsa_circ_239632,RMVar_hsa_circ_239633,RMVar_hsa_circ_239636,RMVar_hsa_circ_312023,RMVar_hsa_circ_347478,RMVar_hsa_circ_372206,RMVar_hsa_circ_72736,RMVar_hsa_circ_360461,RMVar_hsa_circ_274569,RMVar_hsa_circ_239638,RMVar_hsa_circ_41861,RMVar_hsa_circ_239639,RMVar_hsa_circ_346240,RMVar_hsa_circ_325928,RMVar_hsa_circ_300774,RMVar_hsa_circ_304108,RMVar_hsa_circ_282772,RMVar_hsa_circ_7430,RMVar_hsa_circ_20892,RMVar_hsa_circ_270052,RMVar_hsa_circ_20628,RMVar_hsa_circ_239643,RMVar_hsa_circ_239645,RMVar_hsa_circ_239644,RMVar_hsa_circ_239642,RMVar_hsa_circ_239640 49773 RMVar_ID_49773 Human_SNP_ID_282977723 A-to-I Human chr6 + 75645445 75645445 75645445 CGAGGCCAGCCTGGCTGACATGGTGAAACACCATCTCTACTAAAAATAACAAAAATTAGCACAGC CGAGGCCAGCCTGGCTGACATGGTGAAACACCCTCTCTACTAAAAATAACAAAAATTAGCACAGC A C SENP6 Ensembl:ENSG00000112701 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1024609729 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_239641,RMVar_hsa_circ_72907,RMVar_hsa_circ_74039,RMVar_hsa_circ_302921,RMVar_hsa_circ_281774,RMVar_hsa_circ_74233,RMVar_hsa_circ_239632,RMVar_hsa_circ_239633,RMVar_hsa_circ_239636,RMVar_hsa_circ_312023,RMVar_hsa_circ_347478,RMVar_hsa_circ_372206,RMVar_hsa_circ_72736,RMVar_hsa_circ_360461,RMVar_hsa_circ_274569,RMVar_hsa_circ_239638,RMVar_hsa_circ_41861,RMVar_hsa_circ_239639,RMVar_hsa_circ_346240,RMVar_hsa_circ_325928,RMVar_hsa_circ_300774,RMVar_hsa_circ_304108,RMVar_hsa_circ_282772,RMVar_hsa_circ_7430,RMVar_hsa_circ_20892,RMVar_hsa_circ_270052,RMVar_hsa_circ_20628,RMVar_hsa_circ_239643,RMVar_hsa_circ_239645,RMVar_hsa_circ_239644,RMVar_hsa_circ_239642,RMVar_hsa_circ_239640 49774 RMVar_ID_49774 Human_SNP_ID_282977724 A-to-I Human chr6 + 75645445 75645445 75645445 CGAGGCCAGCCTGGCTGACATGGTGAAACACCATCTCTACTAAAAATAACAAAAATTAGCACAGC CGAGGCCAGCCTGGCTGACATGGTGAAACACCGTCTCTACTAAAAATAACAAAAATTAGCACAGC A G SENP6 Ensembl:ENSG00000112701 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1024609729 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_239641,RMVar_hsa_circ_72907,RMVar_hsa_circ_74039,RMVar_hsa_circ_302921,RMVar_hsa_circ_281774,RMVar_hsa_circ_74233,RMVar_hsa_circ_239632,RMVar_hsa_circ_239633,RMVar_hsa_circ_239636,RMVar_hsa_circ_312023,RMVar_hsa_circ_347478,RMVar_hsa_circ_372206,RMVar_hsa_circ_72736,RMVar_hsa_circ_360461,RMVar_hsa_circ_274569,RMVar_hsa_circ_239638,RMVar_hsa_circ_41861,RMVar_hsa_circ_239639,RMVar_hsa_circ_346240,RMVar_hsa_circ_325928,RMVar_hsa_circ_300774,RMVar_hsa_circ_304108,RMVar_hsa_circ_282772,RMVar_hsa_circ_7430,RMVar_hsa_circ_20892,RMVar_hsa_circ_270052,RMVar_hsa_circ_20628,RMVar_hsa_circ_239643,RMVar_hsa_circ_239645,RMVar_hsa_circ_239644,RMVar_hsa_circ_239642,RMVar_hsa_circ_239640 49775 RMVar_ID_49775 Human_SNP_ID_282978667 A-to-I Human chr6 + 75649278 75649278 75649278 CAGAGGTTGCAGTGAGCCGAGATCGCATCACTACGCTCCAGCCTGGGTGACAGAGTGAGACTTGG CAGAGGTTGCAGTGAGCCGAGATCGCATCACTGCGCTCCAGCCTGGGTGACAGAGTGAGACTTGG A G SENP6 Ensembl:ENSG00000112701 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886443224 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26049180 RMVar_hsa_circ_239641,RMVar_hsa_circ_72907,RMVar_hsa_circ_74039,RMVar_hsa_circ_281774,RMVar_hsa_circ_74233,RMVar_hsa_circ_239633,RMVar_hsa_circ_239636,RMVar_hsa_circ_312023,RMVar_hsa_circ_347478,RMVar_hsa_circ_372206,RMVar_hsa_circ_72736,RMVar_hsa_circ_274569,RMVar_hsa_circ_239638,RMVar_hsa_circ_41861,RMVar_hsa_circ_239639,RMVar_hsa_circ_346240,RMVar_hsa_circ_325928,RMVar_hsa_circ_300774,RMVar_hsa_circ_304108,RMVar_hsa_circ_282772,RMVar_hsa_circ_20892,RMVar_hsa_circ_270052,RMVar_hsa_circ_20628,RMVar_hsa_circ_239643,RMVar_hsa_circ_239645,RMVar_hsa_circ_239644,RMVar_hsa_circ_239642,RMVar_hsa_circ_239650,RMVar_hsa_circ_66499,RMVar_hsa_circ_287864,RMVar_hsa_circ_335002,RMVar_hsa_circ_352054,RMVar_hsa_circ_239640,RMVar_hsa_circ_363948,RMVar_hsa_circ_346050,RMVar_hsa_circ_300475,RMVar_hsa_circ_275386,RMVar_hsa_circ_277452,RMVar_hsa_circ_274608,RMVar_hsa_circ_239652,RMVar_hsa_circ_239653,RMVar_hsa_circ_239654,RMVar_hsa_circ_239651,RMVar_hsa_circ_239648,RMVar_hsa_circ_239649 49776 RMVar_ID_49776 Human_SNP_ID_282979902 A-to-I Human chr6 + 75654042 75654042 75654042 GCCCAGGCATTCAAGACCAGACTGGCCAGCATAGTGAGACCCTGTCTCTATAAAATAAAAAAAAA GCCCAGGCATTCAAGACCAGACTGGCCAGCATGGTGAGACCCTGTCTCTATAAAATAAAAAAAAA A G SENP6 Ensembl:ENSG00000112701 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs566151239 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_239641,RMVar_hsa_circ_72907,RMVar_hsa_circ_74039,RMVar_hsa_circ_281774,RMVar_hsa_circ_74233,RMVar_hsa_circ_239633,RMVar_hsa_circ_239636,RMVar_hsa_circ_312023,RMVar_hsa_circ_347478,RMVar_hsa_circ_372206,RMVar_hsa_circ_72736,RMVar_hsa_circ_274569,RMVar_hsa_circ_239638,RMVar_hsa_circ_41861,RMVar_hsa_circ_239639,RMVar_hsa_circ_346240,RMVar_hsa_circ_325928,RMVar_hsa_circ_300774,RMVar_hsa_circ_304108,RMVar_hsa_circ_282772,RMVar_hsa_circ_20892,RMVar_hsa_circ_270052,RMVar_hsa_circ_20628,RMVar_hsa_circ_239643,RMVar_hsa_circ_239645,RMVar_hsa_circ_239644,RMVar_hsa_circ_239642,RMVar_hsa_circ_239650,RMVar_hsa_circ_66499,RMVar_hsa_circ_287864,RMVar_hsa_circ_335002,RMVar_hsa_circ_352054,RMVar_hsa_circ_239640,RMVar_hsa_circ_363948,RMVar_hsa_circ_346050,RMVar_hsa_circ_300475,RMVar_hsa_circ_275386,RMVar_hsa_circ_277452,RMVar_hsa_circ_274608,RMVar_hsa_circ_239652,RMVar_hsa_circ_239653,RMVar_hsa_circ_239654,RMVar_hsa_circ_239651,RMVar_hsa_circ_239648,RMVar_hsa_circ_239649 49777 RMVar_ID_49777 Human_SNP_ID_282981982 A-to-I Human chr6 + 75662387 75662387 75662387 GAACTCTTGGCCCTAAAGAGTCCTACTGCGTCAGCCTCCCAATGTGTTGGGCTTACAGACCTGAG GAACTCTTGGCCCTAAAGAGTCCTACTGCGTCGGCCTCCCAATGTGTTGGGCTTACAGACCTGAG A G SENP6 Ensembl:ENSG00000112701 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879943053 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15879772 RMVar_hsa_circ_239641,RMVar_hsa_circ_72907,RMVar_hsa_circ_281774,RMVar_hsa_circ_74233,RMVar_hsa_circ_239633,RMVar_hsa_circ_239636,RMVar_hsa_circ_312023,RMVar_hsa_circ_347478,RMVar_hsa_circ_372206,RMVar_hsa_circ_72736,RMVar_hsa_circ_274569,RMVar_hsa_circ_239638,RMVar_hsa_circ_239639,RMVar_hsa_circ_346240,RMVar_hsa_circ_300774,RMVar_hsa_circ_304108,RMVar_hsa_circ_282772,RMVar_hsa_circ_20892,RMVar_hsa_circ_270052,RMVar_hsa_circ_20628,RMVar_hsa_circ_239643,RMVar_hsa_circ_239645,RMVar_hsa_circ_239644,RMVar_hsa_circ_239642,RMVar_hsa_circ_239650,RMVar_hsa_circ_66499,RMVar_hsa_circ_335002,RMVar_hsa_circ_352054,RMVar_hsa_circ_239640,RMVar_hsa_circ_363948,RMVar_hsa_circ_346050,RMVar_hsa_circ_300475,RMVar_hsa_circ_275386,RMVar_hsa_circ_277452,RMVar_hsa_circ_274608,RMVar_hsa_circ_239652,RMVar_hsa_circ_239653,RMVar_hsa_circ_239654,RMVar_hsa_circ_239651,RMVar_hsa_circ_239657,RMVar_hsa_circ_271962,RMVar_hsa_circ_239649,RMVar_hsa_circ_303076,RMVar_hsa_circ_330424,RMVar_hsa_circ_332487,RMVar_hsa_circ_311268,RMVar_hsa_circ_298161,RMVar_hsa_circ_265497,RMVar_hsa_circ_270653,RMVar_hsa_circ_239658,RMVar_hsa_circ_239655,RMVar_hsa_circ_239656 49778 RMVar_ID_49778 Human_SNP_ID_282984911 A-to-I Human chr6 + 75673436 75673436 75673436 GCCTCCACCTCACGGGTTCCGGCAATTCTCCTACCTCAGCCTCTTGAGTAGCTGAGATTACAGGT GCCTCCACCTCACGGGTTCCGGCAATTCTCCTGCCTCAGCCTCTTGAGTAGCTGAGATTACAGGT A G SENP6 Ensembl:ENSG00000112701 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1009238610 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_239641,RMVar_hsa_circ_72907,RMVar_hsa_circ_281774,RMVar_hsa_circ_74233,RMVar_hsa_circ_239633,RMVar_hsa_circ_312023,RMVar_hsa_circ_72736,RMVar_hsa_circ_274569,RMVar_hsa_circ_239639,RMVar_hsa_circ_346240,RMVar_hsa_circ_300774,RMVar_hsa_circ_304108,RMVar_hsa_circ_20892,RMVar_hsa_circ_239643,RMVar_hsa_circ_239642,RMVar_hsa_circ_75412,RMVar_hsa_circ_66499,RMVar_hsa_circ_352054,RMVar_hsa_circ_239640,RMVar_hsa_circ_363948,RMVar_hsa_circ_346050,RMVar_hsa_circ_277452,RMVar_hsa_circ_274608,RMVar_hsa_circ_239652,RMVar_hsa_circ_239653,RMVar_hsa_circ_239654,RMVar_hsa_circ_239651,RMVar_hsa_circ_239657,RMVar_hsa_circ_330424,RMVar_hsa_circ_332487,RMVar_hsa_circ_298161,RMVar_hsa_circ_265497,RMVar_hsa_circ_270653,RMVar_hsa_circ_239658,RMVar_hsa_circ_321557,RMVar_hsa_circ_116789,RMVar_hsa_circ_27522,RMVar_hsa_circ_289886,RMVar_hsa_circ_9975,RMVar_hsa_circ_342163,RMVar_hsa_circ_239659,RMVar_hsa_circ_328285,RMVar_hsa_circ_265578,RMVar_hsa_circ_36101,RMVar_hsa_circ_39672,RMVar_hsa_circ_239662,RMVar_hsa_circ_239663,RMVar_hsa_circ_239664,RMVar_hsa_circ_85334,RMVar_hsa_circ_339743,RMVar_hsa_circ_239665,RMVar_hsa_circ_239666,RMVar_hsa_circ_239667 49779 RMVar_ID_49779 Human_SNP_ID_282985023 A-to-I Human chr6 + 75673910 75673910 75673910 GGGTGTGGTGGCGTGCACCCGTAACCCCAGCTACTAGGGAGGCTGAGGCAGAAGAATCACTTGAA GGGTGTGGTGGCGTGCACCCGTAACCCCAGCTGCTAGGGAGGCTGAGGCAGAAGAATCACTTGAA A G SENP6 Ensembl:ENSG00000112701 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1319490852 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_239641,RMVar_hsa_circ_72907,RMVar_hsa_circ_281774,RMVar_hsa_circ_74233,RMVar_hsa_circ_239633,RMVar_hsa_circ_312023,RMVar_hsa_circ_72736,RMVar_hsa_circ_274569,RMVar_hsa_circ_239639,RMVar_hsa_circ_346240,RMVar_hsa_circ_300774,RMVar_hsa_circ_304108,RMVar_hsa_circ_20892,RMVar_hsa_circ_239643,RMVar_hsa_circ_239642,RMVar_hsa_circ_75412,RMVar_hsa_circ_66499,RMVar_hsa_circ_352054,RMVar_hsa_circ_239640,RMVar_hsa_circ_363948,RMVar_hsa_circ_346050,RMVar_hsa_circ_277452,RMVar_hsa_circ_274608,RMVar_hsa_circ_239652,RMVar_hsa_circ_239653,RMVar_hsa_circ_239654,RMVar_hsa_circ_239651,RMVar_hsa_circ_239657,RMVar_hsa_circ_330424,RMVar_hsa_circ_332487,RMVar_hsa_circ_298161,RMVar_hsa_circ_265497,RMVar_hsa_circ_270653,RMVar_hsa_circ_239658,RMVar_hsa_circ_321557,RMVar_hsa_circ_116789,RMVar_hsa_circ_27522,RMVar_hsa_circ_289886,RMVar_hsa_circ_9975,RMVar_hsa_circ_342163,RMVar_hsa_circ_239659,RMVar_hsa_circ_328285,RMVar_hsa_circ_265578,RMVar_hsa_circ_36101,RMVar_hsa_circ_39672,RMVar_hsa_circ_239662,RMVar_hsa_circ_239663,RMVar_hsa_circ_239664,RMVar_hsa_circ_85334,RMVar_hsa_circ_339743,RMVar_hsa_circ_239665,RMVar_hsa_circ_239666,RMVar_hsa_circ_239667 49780 RMVar_ID_49780 Human_SNP_ID_282985221 A-to-I Human chr6 + 75674520 75674520 75674520 ATTTTTTATACTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCATGCTGGTCTTAAACTCTTGG ATTTTTTATACTTTTAGTAGAGATGGGGTTTCTCCATGTTGGCCATGCTGGTCTTAAACTCTTGG A T SENP6 Ensembl:ENSG00000112701 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1218041818 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_239641,RMVar_hsa_circ_72907,RMVar_hsa_circ_281774,RMVar_hsa_circ_74233,RMVar_hsa_circ_239633,RMVar_hsa_circ_312023,RMVar_hsa_circ_72736,RMVar_hsa_circ_274569,RMVar_hsa_circ_239639,RMVar_hsa_circ_346240,RMVar_hsa_circ_300774,RMVar_hsa_circ_304108,RMVar_hsa_circ_20892,RMVar_hsa_circ_239643,RMVar_hsa_circ_239642,RMVar_hsa_circ_75412,RMVar_hsa_circ_66499,RMVar_hsa_circ_352054,RMVar_hsa_circ_239640,RMVar_hsa_circ_363948,RMVar_hsa_circ_346050,RMVar_hsa_circ_277452,RMVar_hsa_circ_274608,RMVar_hsa_circ_239652,RMVar_hsa_circ_239653,RMVar_hsa_circ_239654,RMVar_hsa_circ_239651,RMVar_hsa_circ_239657,RMVar_hsa_circ_330424,RMVar_hsa_circ_332487,RMVar_hsa_circ_298161,RMVar_hsa_circ_265497,RMVar_hsa_circ_270653,RMVar_hsa_circ_239658,RMVar_hsa_circ_321557,RMVar_hsa_circ_116789,RMVar_hsa_circ_27522,RMVar_hsa_circ_289886,RMVar_hsa_circ_9975,RMVar_hsa_circ_342163,RMVar_hsa_circ_239659,RMVar_hsa_circ_328285,RMVar_hsa_circ_265578,RMVar_hsa_circ_36101,RMVar_hsa_circ_39672,RMVar_hsa_circ_239662,RMVar_hsa_circ_239663,RMVar_hsa_circ_239664,RMVar_hsa_circ_85334,RMVar_hsa_circ_339743,RMVar_hsa_circ_239665,RMVar_hsa_circ_239666,RMVar_hsa_circ_239667 49781 RMVar_ID_49781 Human_SNP_ID_282985222 A-to-I Human chr6 + 75674523 75674523 75674523 TTTTATACTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCATGCTGGTCTTAAACTCTTGGGCT TTTTATACTTTTAGTAGAGATGGGGTTTCACCTTGTTGGCCATGCTGGTCTTAAACTCTTGGGCT A T SENP6 Ensembl:ENSG00000112701 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1353414339 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15879907,Human_RBP_ID_26022224 RMVar_hsa_circ_239641,RMVar_hsa_circ_72907,RMVar_hsa_circ_281774,RMVar_hsa_circ_74233,RMVar_hsa_circ_239633,RMVar_hsa_circ_312023,RMVar_hsa_circ_72736,RMVar_hsa_circ_274569,RMVar_hsa_circ_239639,RMVar_hsa_circ_346240,RMVar_hsa_circ_300774,RMVar_hsa_circ_304108,RMVar_hsa_circ_20892,RMVar_hsa_circ_239643,RMVar_hsa_circ_239642,RMVar_hsa_circ_75412,RMVar_hsa_circ_66499,RMVar_hsa_circ_352054,RMVar_hsa_circ_239640,RMVar_hsa_circ_363948,RMVar_hsa_circ_346050,RMVar_hsa_circ_277452,RMVar_hsa_circ_274608,RMVar_hsa_circ_239652,RMVar_hsa_circ_239653,RMVar_hsa_circ_239654,RMVar_hsa_circ_239651,RMVar_hsa_circ_239657,RMVar_hsa_circ_330424,RMVar_hsa_circ_332487,RMVar_hsa_circ_298161,RMVar_hsa_circ_265497,RMVar_hsa_circ_270653,RMVar_hsa_circ_239658,RMVar_hsa_circ_321557,RMVar_hsa_circ_116789,RMVar_hsa_circ_27522,RMVar_hsa_circ_289886,RMVar_hsa_circ_9975,RMVar_hsa_circ_342163,RMVar_hsa_circ_239659,RMVar_hsa_circ_328285,RMVar_hsa_circ_265578,RMVar_hsa_circ_36101,RMVar_hsa_circ_39672,RMVar_hsa_circ_239662,RMVar_hsa_circ_239663,RMVar_hsa_circ_239664,RMVar_hsa_circ_85334,RMVar_hsa_circ_339743,RMVar_hsa_circ_239665,RMVar_hsa_circ_239666,RMVar_hsa_circ_239667 49782 RMVar_ID_49782 Human_SNP_ID_282987015 A-to-I Human chr6 + 75681507 75681507 75681507 TGGAGATGGAGTCTTGCTCTCTCACCCAGTCTACAGTGCAGTGGCGCGATCTTGGCCCACGGCAG TGGAGATGGAGTCTTGCTCTCTCACCCAGTCTGCAGTGCAGTGGCGCGATCTTGGCCCACGGCAG A G SENP6 Ensembl:ENSG00000112701 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1329264203 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_398,RMVar_hsa_circ_239641,RMVar_hsa_circ_72907,RMVar_hsa_circ_346240,RMVar_hsa_circ_300774,RMVar_hsa_circ_304108,RMVar_hsa_circ_20892,RMVar_hsa_circ_239642,RMVar_hsa_circ_66499,RMVar_hsa_circ_239640,RMVar_hsa_circ_346050,RMVar_hsa_circ_277452,RMVar_hsa_circ_239653,RMVar_hsa_circ_239654,RMVar_hsa_circ_330424,RMVar_hsa_circ_332487,RMVar_hsa_circ_298161,RMVar_hsa_circ_265497,RMVar_hsa_circ_239658,RMVar_hsa_circ_27522,RMVar_hsa_circ_9975,RMVar_hsa_circ_342163,RMVar_hsa_circ_328285,RMVar_hsa_circ_265578,RMVar_hsa_circ_36101,RMVar_hsa_circ_239663,RMVar_hsa_circ_239664,RMVar_hsa_circ_239667,RMVar_hsa_circ_364740,RMVar_hsa_circ_42656,RMVar_hsa_circ_7700,RMVar_hsa_circ_48996,RMVar_hsa_circ_239669,RMVar_hsa_circ_239670,RMVar_hsa_circ_75253,RMVar_hsa_circ_66517,RMVar_hsa_circ_239671 49783 RMVar_ID_49783 Human_SNP_ID_282989011 A-to-I Human chr6 + 75689104 75689104 75689104 AAAAATTCAGCTGGGCATGGTGGTGCACACCTATAGTCCTAGCTATTGAGGAGGCTGAGATGGGA AAAAATTCAGCTGGGCATGGTGGTGCACACCTGTAGTCCTAGCTATTGAGGAGGCTGAGATGGGA A G SENP6 Ensembl:ENSG00000112701 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs761721536 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_398,RMVar_hsa_circ_239641,RMVar_hsa_circ_72907,RMVar_hsa_circ_346240,RMVar_hsa_circ_300774,RMVar_hsa_circ_304108,RMVar_hsa_circ_20892,RMVar_hsa_circ_239642,RMVar_hsa_circ_66499,RMVar_hsa_circ_239640,RMVar_hsa_circ_346050,RMVar_hsa_circ_277452,RMVar_hsa_circ_239653,RMVar_hsa_circ_239654,RMVar_hsa_circ_330424,RMVar_hsa_circ_332487,RMVar_hsa_circ_298161,RMVar_hsa_circ_265497,RMVar_hsa_circ_239658,RMVar_hsa_circ_27522,RMVar_hsa_circ_9975,RMVar_hsa_circ_342163,RMVar_hsa_circ_328285,RMVar_hsa_circ_265578,RMVar_hsa_circ_36101,RMVar_hsa_circ_239663,RMVar_hsa_circ_239664,RMVar_hsa_circ_239667,RMVar_hsa_circ_364740,RMVar_hsa_circ_42656,RMVar_hsa_circ_7700,RMVar_hsa_circ_48996,RMVar_hsa_circ_239669,RMVar_hsa_circ_239670,RMVar_hsa_circ_75253,RMVar_hsa_circ_66517,RMVar_hsa_circ_239671 49784 RMVar_ID_49784 Human_SNP_ID_282989015 A-to-I Human chr6 + 75689120 75689118 75689121 ATGGTGGTGCACACCTATAGTCCTAGCTATTGAGGAGGCTGAGATGGGAGGATCACTTGAGCCCA ATGGTGGTGCACACCTATAGTCCTAGCTATT___GAGGCTGAGATGGGAGGATCACTTGAGCCCA TGAG T SENP6 Ensembl:ENSG00000112701 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1367570498 Functional Loss DEL dbSNP153 32..34 33 - - - RMVar_hsa_circ_398,RMVar_hsa_circ_239641,RMVar_hsa_circ_72907,RMVar_hsa_circ_346240,RMVar_hsa_circ_300774,RMVar_hsa_circ_304108,RMVar_hsa_circ_20892,RMVar_hsa_circ_239642,RMVar_hsa_circ_66499,RMVar_hsa_circ_239640,RMVar_hsa_circ_346050,RMVar_hsa_circ_277452,RMVar_hsa_circ_239653,RMVar_hsa_circ_239654,RMVar_hsa_circ_330424,RMVar_hsa_circ_332487,RMVar_hsa_circ_298161,RMVar_hsa_circ_265497,RMVar_hsa_circ_239658,RMVar_hsa_circ_27522,RMVar_hsa_circ_9975,RMVar_hsa_circ_342163,RMVar_hsa_circ_328285,RMVar_hsa_circ_265578,RMVar_hsa_circ_36101,RMVar_hsa_circ_239663,RMVar_hsa_circ_239664,RMVar_hsa_circ_239667,RMVar_hsa_circ_364740,RMVar_hsa_circ_42656,RMVar_hsa_circ_7700,RMVar_hsa_circ_48996,RMVar_hsa_circ_239669,RMVar_hsa_circ_239670,RMVar_hsa_circ_75253,RMVar_hsa_circ_66517,RMVar_hsa_circ_239671 49785 RMVar_ID_49785 Human_SNP_ID_282989283 A-to-I Human chr6 + 75690053 75690053 75690053 CCTGCCTCAGCTTCCTAAGTAGCTGGGACTACAGGTGCACACCGTCACACCCTGCTAATTTTTTC CCTGCCTCAGCTTCCTAAGTAGCTGGGACTACGGGTGCACACCGTCACACCCTGCTAATTTTTTC A G SENP6 Ensembl:ENSG00000112701 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1038390529 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_398,RMVar_hsa_circ_239641,RMVar_hsa_circ_72907,RMVar_hsa_circ_346240,RMVar_hsa_circ_300774,RMVar_hsa_circ_304108,RMVar_hsa_circ_20892,RMVar_hsa_circ_239642,RMVar_hsa_circ_66499,RMVar_hsa_circ_239640,RMVar_hsa_circ_346050,RMVar_hsa_circ_277452,RMVar_hsa_circ_239653,RMVar_hsa_circ_239654,RMVar_hsa_circ_330424,RMVar_hsa_circ_332487,RMVar_hsa_circ_298161,RMVar_hsa_circ_265497,RMVar_hsa_circ_239658,RMVar_hsa_circ_27522,RMVar_hsa_circ_9975,RMVar_hsa_circ_342163,RMVar_hsa_circ_328285,RMVar_hsa_circ_265578,RMVar_hsa_circ_36101,RMVar_hsa_circ_239663,RMVar_hsa_circ_239664,RMVar_hsa_circ_239667,RMVar_hsa_circ_364740,RMVar_hsa_circ_42656,RMVar_hsa_circ_7700,RMVar_hsa_circ_48996,RMVar_hsa_circ_239669,RMVar_hsa_circ_239670,RMVar_hsa_circ_75253,RMVar_hsa_circ_66517,RMVar_hsa_circ_239671 49786 RMVar_ID_49786 Human_SNP_ID_282990830 A-to-I Human chr6 + 75695616 75695616 75695616 AAAATTAGCTGGGCGTGGTGGTGTGTGCCTGTAATCCCAGCTACTTGGGAGGCTGAAGCAGGAGA AAAATTAGCTGGGCGTGGTGGTGTGTGCCTGTCATCCCAGCTACTTGGGAGGCTGAAGCAGGAGA A C SENP6 Ensembl:ENSG00000112701 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1388104563 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_398,RMVar_hsa_circ_239641,RMVar_hsa_circ_72907,RMVar_hsa_circ_346240,RMVar_hsa_circ_300774,RMVar_hsa_circ_304108,RMVar_hsa_circ_20892,RMVar_hsa_circ_239642,RMVar_hsa_circ_66499,RMVar_hsa_circ_239640,RMVar_hsa_circ_346050,RMVar_hsa_circ_277452,RMVar_hsa_circ_239653,RMVar_hsa_circ_239654,RMVar_hsa_circ_330424,RMVar_hsa_circ_332487,RMVar_hsa_circ_298161,RMVar_hsa_circ_265497,RMVar_hsa_circ_239658,RMVar_hsa_circ_27522,RMVar_hsa_circ_9975,RMVar_hsa_circ_342163,RMVar_hsa_circ_328285,RMVar_hsa_circ_265578,RMVar_hsa_circ_36101,RMVar_hsa_circ_239663,RMVar_hsa_circ_239664,RMVar_hsa_circ_239667,RMVar_hsa_circ_364740,RMVar_hsa_circ_42656,RMVar_hsa_circ_7700,RMVar_hsa_circ_48996,RMVar_hsa_circ_239669,RMVar_hsa_circ_239670,RMVar_hsa_circ_75253,RMVar_hsa_circ_66517,RMVar_hsa_circ_239671 49787 RMVar_ID_49787 Human_SNP_ID_282993521 A-to-I Human chr6 + 75706016 75706016 75706016 TGGAGTGCAGTGGCGTAATCTTGTCTCACTGCAACCTCCCCCTCCTGGGTTCAAGAGATTGTCTT TGGAGTGCAGTGGCGTAATCTTGTCTCACTGCGACCTCCCCCTCCTGGGTTCAAGAGATTGTCTT A G SENP6 Ensembl:ENSG00000112701 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956299214 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7629178 RMVar_hsa_circ_398,RMVar_hsa_circ_239641,RMVar_hsa_circ_346240,RMVar_hsa_circ_304108,RMVar_hsa_circ_239640,RMVar_hsa_circ_239654,RMVar_hsa_circ_330424,RMVar_hsa_circ_265497,RMVar_hsa_circ_27522,RMVar_hsa_circ_265578,RMVar_hsa_circ_239664,RMVar_hsa_circ_239667,RMVar_hsa_circ_42656,RMVar_hsa_circ_100193,RMVar_hsa_circ_41365,RMVar_hsa_circ_48996,RMVar_hsa_circ_239669,RMVar_hsa_circ_239670,RMVar_hsa_circ_75253,RMVar_hsa_circ_66517,RMVar_hsa_circ_239671,RMVar_hsa_circ_349661,RMVar_hsa_circ_239674,RMVar_hsa_circ_22875,RMVar_hsa_circ_239677,RMVar_hsa_circ_289101,RMVar_hsa_circ_277815,RMVar_hsa_circ_239679,RMVar_hsa_circ_239681,RMVar_hsa_circ_98305,RMVar_hsa_circ_239682,RMVar_hsa_circ_239680,RMVar_hsa_circ_239683 49788 RMVar_ID_49788 Human_SNP_ID_282993873 A-to-I Human chr6 + 75707543 75707543 75707543 GTGTCACCTGCCCGGCAAAATTTATTTTCTGTAGAGACGGGCTCACTTTGTTGCCCAGGCTGGTC GTGTCACCTGCCCGGCAAAATTTATTTTCTGTGGAGACGGGCTCACTTTGTTGCCCAGGCTGGTC A G SENP6 Ensembl:ENSG00000112701 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs956354115 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15880295 RMVar_hsa_circ_398,RMVar_hsa_circ_239641,RMVar_hsa_circ_346240,RMVar_hsa_circ_304108,RMVar_hsa_circ_239640,RMVar_hsa_circ_239654,RMVar_hsa_circ_330424,RMVar_hsa_circ_265497,RMVar_hsa_circ_27522,RMVar_hsa_circ_265578,RMVar_hsa_circ_239664,RMVar_hsa_circ_239667,RMVar_hsa_circ_42656,RMVar_hsa_circ_100193,RMVar_hsa_circ_41365,RMVar_hsa_circ_48996,RMVar_hsa_circ_239669,RMVar_hsa_circ_239670,RMVar_hsa_circ_75253,RMVar_hsa_circ_66517,RMVar_hsa_circ_239671,RMVar_hsa_circ_349661,RMVar_hsa_circ_239674,RMVar_hsa_circ_22875,RMVar_hsa_circ_239677,RMVar_hsa_circ_289101,RMVar_hsa_circ_277815,RMVar_hsa_circ_239679,RMVar_hsa_circ_239681,RMVar_hsa_circ_98305,RMVar_hsa_circ_239682,RMVar_hsa_circ_239680,RMVar_hsa_circ_239683 49789 RMVar_ID_49789 Human_SNP_ID_282994831 A-to-I Human chr6 + 75711907 75711907 75711907 GTTGGCAAGACTGATCTCAAACTCCTGGCCTCAAGTGATCCGCCCCTCTGAGCCTTCCAAATTGC GTTGGCAAGACTGATCTCAAACTCCTGGCCTCGAGTGATCCGCCCCTCTGAGCCTTCCAAATTGC A G SENP6 Ensembl:ENSG00000112701 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285774442 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_330424,RMVar_hsa_circ_265497,RMVar_hsa_circ_265578,RMVar_hsa_circ_239667,RMVar_hsa_circ_100193,RMVar_hsa_circ_75253,RMVar_hsa_circ_22875,RMVar_hsa_circ_239681,RMVar_hsa_circ_98305,RMVar_hsa_circ_239682,RMVar_hsa_circ_23660,RMVar_hsa_circ_13926 49790 RMVar_ID_49790 Human_SNP_ID_283005545 A-to-I Human chr6 + 75756153 75756153 75756153 ACGGTGATGCTTACCTGTAGTCCTAGCTACTCAGGCGGCTGAGGCAGGAGGAATGCTTGAGCCCA ACGGTGATGCTTACCTGTAGTCCTAGCTACTCCGGCGGCTGAGGCAGGAGGAATGCTTGAGCCCA A C MYO6 Ensembl:ENSG00000196586 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1197830972 Functional Loss SNV dbSNP153 33..33 33 - - - 49791 RMVar_ID_49791 Human_SNP_ID_283037610 A-to-I Human chr6 + 75890142 75890142 75890142 AAGCTCAGAGGAACTCCTCAGTGCATTACAGAAAAAAAAACAGCAGGAAGAGGAAGCAGAAAGGC AAGCTCAGAGGAACTCCTCAGTGCATTACAGAGAAAAAAACAGCAGGAAGAGGAAGCAGAAAGGC A G MYO6 Ensembl:ENSG00000196586 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1562290928 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 49792 RMVar_ID_49792 Human_SNP_ID_283375769 A-to-I Human chr6 - 77124477 77124477 77124477 TCCAGGATAGTGAGTGCTCCAGATTTATGGATATCTGCCTGGCCATGAAGCAAAGAGGACCCCTG TCCAGGATAGTGAGTGCTCCAGATTTATGGATGTCTGCCTGGCCATGAAGCAAAGAGGACCCCTG T 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:URS00009AEF87,RNACentral:URS00008BA766,RNACentral:URS0000D5742D lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1004217825 Functional Loss SNV dbSNP153 33..33 33 - - - 49793 RMVar_ID_49793 Human_SNP_ID_283834677 A-to-I Human chr6 + 78889013 78889013 78889013 ATGGCATGCACCTGTAGACCCATCTACTCTGGAAGCTGGGGTGGGAGGATTGCTTGAGCCCAGGA ATGGCATGCACCTGTAGACCCATCTACTCTGGCAGCTGGGGTGGGAGGATTGCTTGAGCCCAGGA A C IRAK1BP1 Ensembl:ENSG00000146243 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1336763316 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15043 49794 RMVar_ID_49794 Human_SNP_ID_283834688 A-to-I Human chr6 + 78889066 78889066 78889066 TTGAGCCCAGGAGGCAGAGGTTCCAATGAGTCAAGATCATGCCACTGCACTGCAGCCTGGGCAAC TTGAGCCCAGGAGGCAGAGGTTCCAATGAGTCGAGATCATGCCACTGCACTGCAGCCTGGGCAAC A G IRAK1BP1 Ensembl:ENSG00000146243 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1449269263 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15043 49795 RMVar_ID_49795 Human_SNP_ID_283836660 A-to-I Human chr6 + 78896809 78896806 78896810 ATCACACCACTGCACTCCAGCCAGGAAAACAGAAAGAGACCCTGGCTCAAAAAAAAAAAAAAATT ATCACACCACTGCACTCCAGCCAGGAAAAC____AGAGACCCTGGCTCAAAAAAAAAAAAAAATT CAGAA C IRAK1BP1 Ensembl:ENSG00000146243 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1222232044 Functional Loss DEL dbSNP153 31..34 33 - - - RMVar_hsa_circ_15043 49796 RMVar_ID_49796 Human_SNP_ID_283837478 A-to-I Human chr6 + 78899647 78899647 78899647 TCGCCCAAGCTGGAGTGCAGTGGTACGATCTCAGCTCACTGCAACCTCTGCCTCCTGAATTTAAG TCGCCCAAGCTGGAGTGCAGTGGTACGATCTCGGCTCACTGCAACCTCTGCCTCCTGAATTTAAG A G IRAK1BP1 Ensembl:ENSG00000146243 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1213363233 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15043,RMVar_hsa_circ_239718,RMVar_hsa_circ_239719,RMVar_hsa_circ_303237 49797 RMVar_ID_49797 Human_SNP_ID_283838055 A-to-I Human chr6 + 78902336 78902336 78902336 GGCTAATTTTTTATTAGTGATAAGGTCTTGCTATGTTGCCCAGGCTGGTCTCAAACTCCTGGCTT GGCTAATTTTTTATTAGTGATAAGGTCTTGCTGTGTTGCCCAGGCTGGTCTCAAACTCCTGGCTT A G IRAK1BP1 Ensembl:ENSG00000146243 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs948886112 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15043,RMVar_hsa_circ_239718,RMVar_hsa_circ_239719,RMVar_hsa_circ_303237 49798 RMVar_ID_49798 Human_SNP_ID_283838100 A-to-I Human chr6 + 78902516 78902516 78902516 CGGGTAGGCCAGGCACGTTGGCTCACGCCTGTAATCCCAGCACTTGGGAGGCCGAGGTAGGCAGA CGGGTAGGCCAGGCACGTTGGCTCACGCCTGTGATCCCAGCACTTGGGAGGCCGAGGTAGGCAGA A G IRAK1BP1 Ensembl:ENSG00000146243 Protein coding 3'UTR GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs973075808 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15043,RMVar_hsa_circ_239718,RMVar_hsa_circ_239719,RMVar_hsa_circ_303237 49799 RMVar_ID_49799 Human_SNP_ID_283849863 A-to-I Human chr6 - 78949885 78949885 78949885 CAGGAGTTTGAGACCAGTCTGAGCAATATGGCAAAACCCCGTCTTTACAAAAAATACAAAAATTA CAGGAGTTTGAGACCAGTCTGAGCAATATGGCTAAACCCCGTCTTTACAAAAAATACAAAAATTA T A PHIP Ensembl:ENSG00000146247 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1356809657 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11310,RMVar_hsa_circ_38104,RMVar_hsa_circ_266789,RMVar_hsa_circ_23539,RMVar_hsa_circ_37584,RMVar_hsa_circ_158,RMVar_hsa_circ_119691,RMVar_hsa_circ_38235,RMVar_hsa_circ_239720,RMVar_hsa_circ_83904,RMVar_hsa_circ_266468,RMVar_hsa_circ_239722 49800 RMVar_ID_49800 Human_SNP_ID_283850400 A-to-I Human chr6 - 78952236 78952236 78952236 TTGTATATTTTTAGTAGAGGTGGGGTTTCACCATGTTGGCCAGGATGGTCTCAATCTCTTGACCT TTGTATATTTTTAGTAGAGGTGGGGTTTCACCGTGTTGGCCAGGATGGTCTCAATCTCTTGACCT T C PHIP Ensembl:ENSG00000146247 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1323296611 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11310,RMVar_hsa_circ_38104,RMVar_hsa_circ_266789,RMVar_hsa_circ_23539,RMVar_hsa_circ_37584,RMVar_hsa_circ_158,RMVar_hsa_circ_119691,RMVar_hsa_circ_38235,RMVar_hsa_circ_239720,RMVar_hsa_circ_83904,RMVar_hsa_circ_266468,RMVar_hsa_circ_239722 49801 RMVar_ID_49801 Human_SNP_ID_283861329 A-to-I Human chr6 - 78994508 78994508 78994508 CAGTGGCGTGATCTCGGCTCACCGCAACATCCACCTCCCAGTTTCAAGCAATTCCCCTGCCTCAG CAGTGGCGTGATCTCGGCTCACCGCAACATCCGCCTCCCAGTTTCAAGCAATTCCCCTGCCTCAG T C PHIP Ensembl:ENSG00000146247 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031836159 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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_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_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_78432,RMVar_hsa_circ_60246,RMVar_hsa_circ_239744,RMVar_hsa_circ_239745,RMVar_hsa_circ_94595,RMVar_hsa_circ_305761,RMVar_hsa_circ_239747 49802 RMVar_ID_49802 Human_SNP_ID_283867466 A-to-I Human chr6 - 79021284 79021284 79021284 GAATTAGCCGGGCATGGTGGTGCACACCTGTAATCCCAGCTACTTGGGAGGCTGAGGCATGAGAA GAATTAGCCGGGCATGGTGGTGCACACCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCATGAGAA T C PHIP Ensembl:ENSG00000146247 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1158993750 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_731,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_239729,RMVar_hsa_circ_373368,RMVar_hsa_circ_49870,RMVar_hsa_circ_122781,RMVar_hsa_circ_239732,RMVar_hsa_circ_361991,RMVar_hsa_circ_52827,RMVar_hsa_circ_239733,RMVar_hsa_circ_115427,RMVar_hsa_circ_239736,RMVar_hsa_circ_84810,RMVar_hsa_circ_266050,RMVar_hsa_circ_239742,RMVar_hsa_circ_239739,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_329594,RMVar_hsa_circ_44898,RMVar_hsa_circ_71739,RMVar_hsa_circ_335187,RMVar_hsa_circ_18950,RMVar_hsa_circ_239743,RMVar_hsa_circ_100333,RMVar_hsa_circ_367740,RMVar_hsa_circ_78432,RMVar_hsa_circ_60246,RMVar_hsa_circ_239744,RMVar_hsa_circ_94595,RMVar_hsa_circ_298585,RMVar_hsa_circ_339378,RMVar_hsa_circ_239747,RMVar_hsa_circ_52992,RMVar_hsa_circ_106677,RMVar_hsa_circ_4575,RMVar_hsa_circ_239750,RMVar_hsa_circ_239752,RMVar_hsa_circ_108664,RMVar_hsa_circ_31499,RMVar_hsa_circ_239755,RMVar_hsa_circ_239757,RMVar_hsa_circ_271169,RMVar_hsa_circ_352513,RMVar_hsa_circ_316966,RMVar_hsa_circ_281697,RMVar_hsa_circ_85474,RMVar_hsa_circ_239759,RMVar_hsa_circ_239758,RMVar_hsa_circ_91950,RMVar_hsa_circ_239756,RMVar_hsa_circ_239762,RMVar_hsa_circ_64493,RMVar_hsa_circ_45465,RMVar_hsa_circ_75224,RMVar_hsa_circ_87452,RMVar_hsa_circ_344520,RMVar_hsa_circ_239764,RMVar_hsa_circ_348971,RMVar_hsa_circ_239765,RMVar_hsa_circ_30675 49803 RMVar_ID_49803 Human_SNP_ID_283878791 A-to-I Human chr6 - 79068297 79068297 79068297 CACCACGTCCGGCTAATTTTTGTATTTTTGGTAGAGACGGGGTTTCACCATGCTGGCAGGGCTGG CACCACGTCCGGCTAATTTTTGTATTTTTGGTGGAGACGGGGTTTCACCATGCTGGCAGGGCTGG T C PHIP Ensembl:ENSG00000146247 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1274150132 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7631770,Human_RBP_ID_15884532 RMVar_hsa_circ_104838,RMVar_hsa_circ_239727,RMVar_hsa_circ_5281,RMVar_hsa_circ_4575,RMVar_hsa_circ_372446,RMVar_hsa_circ_239770 49804 RMVar_ID_49804 Human_SNP_ID_283970268 A-to-I Human chr6 + 79437034 79437034 79437034 CACTTGGTCTTGCCTTTGAAATCCAACATCCCAGGCCATTCTGTATTTATGTCGCCCACAGTTGC CACTTGGTCTTGCCTTTGAAATCCAACATCCCGGGCCATTCTGTATTTATGTCGCCCACAGTTGC A G AL391840.1 Ensembl:ENSG00000231533 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1003550473 Functional Loss SNV dbSNP153 33..33 33 - - - 49805 RMVar_ID_49805 Human_SNP_ID_283970269 A-to-I Human chr6 + 79437039 79437039 79437039 GGTCTTGCCTTTGAAATCCAACATCCCAGGCCATTCTGTATTTATGTCGCCCACAGTTGCTTGTT GGTCTTGCCTTTGAAATCCAACATCCCAGGCCGTTCTGTATTTATGTCGCCCACAGTTGCTTGTT A G AL391840.1 Ensembl:ENSG00000231533 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs11547637 Functional Loss SNV dbSNP153 33..33 33 - - - 49806 RMVar_ID_49806 Human_SNP_ID_283995825 A-to-I Human chr6 + 79542409 79542409 79542409 ATTCTGCCTCAGCCTCCTAGATAGTTGGGATTACAGGCATGCACCACCACACCCAGCTAATTTTG ATTCTGCCTCAGCCTCCTAGATAGTTGGGATTGCAGGCATGCACCACCACACCCAGCTAATTTTG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1365281424 Functional Loss SNV dbSNP153 33..33 33 - - - 49807 RMVar_ID_49807 Human_SNP_ID_283998046 A-to-I Human chr6 + 79551970 79551970 79551970 AAAATTAGCCGGGTGTGGTGGTGGGCACCTGTATTCTTGGATGCCTGGGAAGCTGAGGCACAAAA AAAATTAGCCGGGTGTGGTGGTGGGCACCTGTGTTCTTGGATGCCTGGGAAGCTGAGGCACAAAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs891049968 Functional Loss SNV dbSNP153 33..33 33 - - - 49808 RMVar_ID_49808 Human_SNP_ID_284093978 A-to-I Human chr6 + 79953985 79953985 79953985 CTGATGACCAGGCGCCCAATACAACCAAATCCATTGACTCCAACCTTCACTTTCCCCATGGTGTC CTGATGACCAGGCGCCCAATACAACCAAATCCGTTGACTCCAACCTTCACTTTCCCCATGGTGTC A G AL133475.1 Ensembl:ENSG00000287816 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1247922213 Functional Loss SNV dbSNP153 33..33 33 - - - 49809 RMVar_ID_49809 Human_SNP_ID_284093979 A-to-I Human chr6 + 79953985 79953985 79953985 CTGATGACCAGGCGCCCAATACAACCAAATCCATTGACTCCAACCTTCACTTTCCCCATGGTGTC CTGATGACCAGGCGCCCAATACAACCAAATCCTTTGACTCCAACCTTCACTTTCCCCATGGTGTC A T AL133475.1 Ensembl:ENSG00000287816 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1247922213 Functional Loss SNV dbSNP153 33..33 33 - - - 49810 RMVar_ID_49810 Human_SNP_ID_284111938 A-to-I Human chr6 + 80028395 80028395 80028395 GCTGGAGTGCAGTGGCGCGATCTCGGGTGACTACAACCTCTGCTTCCCAGGTTCAAGCGATTCTC GCTGGAGTGCAGTGGCGCGATCTCGGGTGACTGCAACCTCTGCTTCCCAGGTTCAAGCGATTCTC A G TTK Ensembl:ENSG00000112742 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs972055461 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15886599 RMVar_hsa_circ_10268,RMVar_hsa_circ_365223,RMVar_hsa_circ_30964,RMVar_hsa_circ_19908,RMVar_hsa_circ_10466,RMVar_hsa_circ_239790,RMVar_hsa_circ_315491 49811 RMVar_ID_49811 Human_SNP_ID_284134660 A-to-I Human chr6 + 80119156 80119156 80119156 ACTAAAAATACAAAAAAATTAGCAGGCATGCTAGCGCATGCCTGTAATCCCTGGGGTGGCTGTGG ACTAAAAATACAAAAAAATTAGCAGGCATGCTGGCGCATGCCTGTAATCCCTGGGGTGGCTGTGG A G BCKDHB Ensembl:ENSG00000083123 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1278341191 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88367,RMVar_hsa_circ_239792 49812 RMVar_ID_49812 Human_SNP_ID_284196251 A-to-I Human chr6 + 80377089 80377089 80377089 TTGATGAAGTCTCACTCTGTCATGCCCAGGCTAGAGTTTAGTGGTACAATCTTGGCTCACTGCAA TTGATGAAGTCTCACTCTGTCATGCCCAGGCTGGAGTTTAGTGGTACAATCTTGGCTCACTGCAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1374931205 Functional Loss SNV dbSNP153 33..33 33 - - - 49813 RMVar_ID_49813 Human_SNP_ID_284897928 A-to-I Human chr6 - 83033181 83033181 83033181 GCCTATGAGATCTGGTTTTTTAAAAGTGTGTAACACCTCTCCCCTCTCTCTCTCATCCCTGCTTT GCCTATGAGATCTGGTTTTTTAAAAGTGTGTAGCACCTCTCCCCTCTCTCTCTCATCCCTGCTTT T C UBE3D Ensembl:ENSG00000118420 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1372355510 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_272079,RMVar_hsa_circ_288773,RMVar_hsa_circ_276616,RMVar_hsa_circ_7578,RMVar_hsa_circ_107017,RMVar_hsa_circ_239853,RMVar_hsa_circ_239855,RMVar_hsa_circ_239856,RMVar_hsa_circ_239854,RMVar_hsa_circ_10871,RMVar_hsa_circ_21975,RMVar_hsa_circ_314870,RMVar_hsa_circ_325505,RMVar_hsa_circ_318350,RMVar_hsa_circ_307183,RMVar_hsa_circ_239858,RMVar_hsa_circ_239859,RMVar_hsa_circ_378176,RMVar_hsa_circ_239857,RMVar_hsa_circ_239860,RMVar_hsa_circ_239861 49814 RMVar_ID_49814 Human_SNP_ID_284898348 A-to-I Human chr6 - 83034979 83034979 83034979 TGGGGTCTCCATATGTTGCCCAGGCTGATCTTAAACTCCAGGACTCAAGTGATCCTCCTGCCTCA TGGGGTCTCCATATGTTGCCCAGGCTGATCTTGAACTCCAGGACTCAAGTGATCCTCCTGCCTCA T C UBE3D Ensembl:ENSG00000118420 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1280278028 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_272079,RMVar_hsa_circ_288773,RMVar_hsa_circ_276616,RMVar_hsa_circ_7578,RMVar_hsa_circ_107017,RMVar_hsa_circ_239853,RMVar_hsa_circ_239855,RMVar_hsa_circ_239856,RMVar_hsa_circ_239854,RMVar_hsa_circ_10871,RMVar_hsa_circ_21975,RMVar_hsa_circ_314870,RMVar_hsa_circ_325505,RMVar_hsa_circ_318350,RMVar_hsa_circ_307183,RMVar_hsa_circ_239858,RMVar_hsa_circ_239859,RMVar_hsa_circ_378176,RMVar_hsa_circ_239857,RMVar_hsa_circ_239860,RMVar_hsa_circ_239861 49815 RMVar_ID_49815 Human_SNP_ID_284898367 A-to-I Human chr6 - 83035059 83035059 83035059 CTCCCATCTCAGCCTCCCAAGTAGCCGGGACCACAGGTGCATACCACCATGTCTGACTAATTTTT CTCCCATCTCAGCCTCCCAAGTAGCCGGGACCCCAGGTGCATACCACCATGTCTGACTAATTTTT T G UBE3D Ensembl:ENSG00000118420 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1479616904 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_272079,RMVar_hsa_circ_288773,RMVar_hsa_circ_276616,RMVar_hsa_circ_7578,RMVar_hsa_circ_107017,RMVar_hsa_circ_239853,RMVar_hsa_circ_239855,RMVar_hsa_circ_239856,RMVar_hsa_circ_239854,RMVar_hsa_circ_10871,RMVar_hsa_circ_21975,RMVar_hsa_circ_314870,RMVar_hsa_circ_325505,RMVar_hsa_circ_318350,RMVar_hsa_circ_307183,RMVar_hsa_circ_239858,RMVar_hsa_circ_239859,RMVar_hsa_circ_378176,RMVar_hsa_circ_239857,RMVar_hsa_circ_239860,RMVar_hsa_circ_239861 49816 RMVar_ID_49816 Human_SNP_ID_284899553 A-to-I Human chr6 - 83039915 83039915 83039915 ACACAGTAGGCCTGGTGTGGTGGCTCACGCCTATAGTCCCAGCACTTAGGGAGGCCAAGGTGGGT ACACAGTAGGCCTGGTGTGGTGGCTCACGCCTGTAGTCCCAGCACTTAGGGAGGCCAAGGTGGGT T C UBE3D Ensembl:ENSG00000118420 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs992865113 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26026756 RMVar_hsa_circ_288773,RMVar_hsa_circ_276616,RMVar_hsa_circ_7578,RMVar_hsa_circ_107017,RMVar_hsa_circ_239855,RMVar_hsa_circ_239856,RMVar_hsa_circ_239854,RMVar_hsa_circ_1896,RMVar_hsa_circ_10871,RMVar_hsa_circ_21975,RMVar_hsa_circ_325505,RMVar_hsa_circ_318350,RMVar_hsa_circ_307183,RMVar_hsa_circ_239858,RMVar_hsa_circ_239859,RMVar_hsa_circ_378176,RMVar_hsa_circ_42929,RMVar_hsa_circ_239860,RMVar_hsa_circ_239861,RMVar_hsa_circ_15247 49817 RMVar_ID_49817 Human_SNP_ID_284899643 A-to-I Human chr6 - 83040259 83040259 83040259 CTGCCTCAGCCTCCTGAGTAGCTGGGACTACAAGCGCGCACCACGACGCCCAGCTAATTTTTATA CTGCCTCAGCCTCCTGAGTAGCTGGGACTACATGCGCGCACCACGACGCCCAGCTAATTTTTATA T A UBE3D Ensembl:ENSG00000118420 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs570323861 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_288773,RMVar_hsa_circ_276616,RMVar_hsa_circ_7578,RMVar_hsa_circ_107017,RMVar_hsa_circ_239855,RMVar_hsa_circ_239856,RMVar_hsa_circ_239854,RMVar_hsa_circ_1896,RMVar_hsa_circ_10871,RMVar_hsa_circ_21975,RMVar_hsa_circ_325505,RMVar_hsa_circ_318350,RMVar_hsa_circ_307183,RMVar_hsa_circ_239858,RMVar_hsa_circ_239859,RMVar_hsa_circ_378176,RMVar_hsa_circ_42929,RMVar_hsa_circ_239860,RMVar_hsa_circ_239861,RMVar_hsa_circ_15247 49818 RMVar_ID_49818 Human_SNP_ID_284918072 A-to-I Human chr6 + 83117220 83117220 83117220 TCACCTAGGCTGGAGTGCAGTGGTGCTATCTTAGCTCACTGCAACCTCTGCCTCCAGGGTTCGAG TCACCTAGGCTGGAGTGCAGTGGTGCTATCTTGGCTCACTGCAACCTCTGCCTCCAGGGTTCGAG A G DOP1A Ensembl:ENSG00000083097 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1372753685 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9503,RMVar_hsa_circ_329141,RMVar_hsa_circ_334333,RMVar_hsa_circ_313310,RMVar_hsa_circ_43027,RMVar_hsa_circ_55608,RMVar_hsa_circ_11996,RMVar_hsa_circ_239869,RMVar_hsa_circ_239870,RMVar_hsa_circ_15655,RMVar_hsa_circ_239872,RMVar_hsa_circ_375537,RMVar_hsa_circ_43529,RMVar_hsa_circ_65831,RMVar_hsa_circ_85977,RMVar_hsa_circ_239873,RMVar_hsa_circ_76633,RMVar_hsa_circ_123371,RMVar_hsa_circ_239877,RMVar_hsa_circ_239876,RMVar_hsa_circ_320310,RMVar_hsa_circ_49433,RMVar_hsa_circ_87758,RMVar_hsa_circ_45227,RMVar_hsa_circ_18602,RMVar_hsa_circ_37359,RMVar_hsa_circ_239879,RMVar_hsa_circ_239881,RMVar_hsa_circ_239882,RMVar_hsa_circ_239880,RMVar_hsa_circ_239878 49819 RMVar_ID_49819 Human_SNP_ID_284955994 A-to-I Human chr6 - 83276012 83276012 83276012 TAATTCCAGCAGTTCCGGAGACCGAGACGGGCAGATCACGAGGTCAGAAGATCGCGACCATCCTG TAATTCCAGCAGTTCCGGAGACCGAGACGGGCGGATCACGAGGTCAGAAGATCGCGACCATCCTG T C ME1 Ensembl:ENSG00000065833 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1397191021 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_31154,RMVar_hsa_circ_91621,RMVar_hsa_circ_239910,RMVar_hsa_circ_31366,RMVar_hsa_circ_369203,RMVar_hsa_circ_239914 49820 RMVar_ID_49820 Human_SNP_ID_284956544 A-to-I Human chr6 - 83278544 83278544 83278544 ACAGTTAGTTGAGAGGCTGAGACAGGAGGATCACTTGAGCCCAGGAGTTCTAGGTTACAGTGAGC ACAGTTAGTTGAGAGGCTGAGACAGGAGGATCCCTTGAGCCCAGGAGTTCTAGGTTACAGTGAGC T G ME1 Ensembl:ENSG00000065833 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170841218 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_31154,RMVar_hsa_circ_91621,RMVar_hsa_circ_239910,RMVar_hsa_circ_31366,RMVar_hsa_circ_369203,RMVar_hsa_circ_239914 49821 RMVar_ID_49821 Human_SNP_ID_284982390 A-to-I Human chr6 - 83388212 83388210 83388212 TGTGGTGGTGCGTGCTATAGTCCCACCTACTCAGGGGGCTGAGGTGGGAGGATTGCTTGAGCCTG TGTGGTGGTGCGTGCTATAGTCCCACCTACTC__GGGGCTGAGGTGGGAGGATTGCTTGAGCCTG CCT C ME1 Ensembl:ENSG00000065833 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs934643950 Functional Loss DEL dbSNP153 33..34 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 49822 RMVar_ID_49822 Human_SNP_ID_284982391 A-to-I Human chr6 - 83388212 83388212 83388212 TGTGGTGGTGCGTGCTATAGTCCCACCTACTCAGGGGGCTGAGGTGGGAGGATTGCTTGAGCCTG TGTGGTGGTGCGTGCTATAGTCCCACCTACTCGGGGGGCTGAGGTGGGAGGATTGCTTGAGCCTG T C ME1 Ensembl:ENSG00000065833 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs995796077 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 49823 RMVar_ID_49823 Human_SNP_ID_285447607 A-to-I Human chr6 - 85286387 85286387 85286387 CACTTAATTAAATTCGTTGATTATCACTTGAAACATTTTGAACAATAGCTTCTAGAGAGTTACTT CACTTAATTAAATTCGTTGATTATCACTTGAAGCATTTTGAACAATAGCTTCTAGAGAGTTACTT T C HSALNG0051675 RNACentral:URS0000EB1FE6 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1276879613 Functional Loss SNV dbSNP153 33..33 33 - - - 49824 RMVar_ID_49824 Human_SNP_ID_285447613 A-to-I Human chr6 - 85286400 85286397 85286401 GCAGCTTGAACTGCACTTAATTAAATTCGTTGATTATCACTTGAAACATTTTGAACAATAGCTTC GCAGCTTGAACTGCACTTAATTAAATTCGTT____ATCACTTGAAACATTTTGAACAATAGCTTC TAATC T HSALNG0051675 RNACentral:URS0000EB1FE6 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1220727380 Functional Loss DEL dbSNP153 32..35 33 - - - 49825 RMVar_ID_49825 Human_SNP_ID_285447614 A-to-I Human chr6 - 85286400 85286400 85286400 GCAGCTTGAACTGCACTTAATTAAATTCGTTGATTATCACTTGAAACATTTTGAACAATAGCTTC GCAGCTTGAACTGCACTTAATTAAATTCGTTGTTTATCACTTGAAACATTTTGAACAATAGCTTC T A HSALNG0051675 RNACentral:URS0000EB1FE6 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs554859496 Functional Loss SNV dbSNP153 33..33 33 - - - 49826 RMVar_ID_49826 Human_SNP_ID_285447790 A-to-I Human chr6 - 85287160 85287160 85287160 TCAAGACTGTATCTACCAATATATTTACGTCTATGTGATGAATTAAAACACAAAGGGCTGGAAGA TCAAGACTGTATCTACCAATATATTTACGTCTGTGTGATGAATTAAAACACAAAGGGCTGGAAGA T C HSALNG0051675 RNACentral:URS0000EB1FE6 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1252836585 Functional Loss SNV dbSNP153 33..33 33 - - - 49827 RMVar_ID_49827 Human_SNP_ID_285447860 A-to-I Human chr6 - 85287451 85287451 85287451 GCCTGTACCTGCTGCTGACTTCCTGCAGTGATATTAGAGAGGAACCACACTGCTTCTTTATTGAT GCCTGTACCTGCTGCTGACTTCCTGCAGTGATGTTAGAGAGGAACCACACTGCTTCTTTATTGAT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202941648 Functional Loss SNV dbSNP153 33..33 33 - - - 49828 RMVar_ID_49828 Human_SNP_ID_285484392 A-to-I Human chr6 + 85427954 85427954 85427954 GGAGAACATCTCATCATGGCTGATGAGGTCCCAGTAGATAAATCATGATGGTGGCTGAAGGCAGA GGAGAACATCTCATCATGGCTGATGAGGTCCCGGTAGATAAATCATGATGGTGGCTGAAGGCAGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1303199255 Functional Loss SNV dbSNP153 33..33 33 - - - 49829 RMVar_ID_49829 Human_SNP_ID_285505025 A-to-I Human chr6 - 85515145 85515145 85515145 CTCCTGCCTCAGTCTCCCAAGTAGCTGGGACTACAGGCACGCATCACTACACCTGGCTAATTTTT CTCCTGCCTCAGTCTCCCAAGTAGCTGGGACTGCAGGCACGCATCACTACACCTGGCTAATTTTT T C SNX14 Ensembl:ENSG00000135317 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900236158 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_788,RMVar_hsa_circ_276806,RMVar_hsa_circ_319549,RMVar_hsa_circ_327319,RMVar_hsa_circ_350893,RMVar_hsa_circ_331773,RMVar_hsa_circ_313890,RMVar_hsa_circ_316419,RMVar_hsa_circ_287418,RMVar_hsa_circ_102147,RMVar_hsa_circ_49241,RMVar_hsa_circ_35029,RMVar_hsa_circ_37864,RMVar_hsa_circ_239988,RMVar_hsa_circ_239990,RMVar_hsa_circ_239992,RMVar_hsa_circ_239993,RMVar_hsa_circ_239991,RMVar_hsa_circ_239989,RMVar_hsa_circ_361057,RMVar_hsa_circ_55344,RMVar_hsa_circ_109809,RMVar_hsa_circ_324423,RMVar_hsa_circ_345569,RMVar_hsa_circ_275106,RMVar_hsa_circ_49914,RMVar_hsa_circ_239995,RMVar_hsa_circ_239997,RMVar_hsa_circ_14651,RMVar_hsa_circ_239996,RMVar_hsa_circ_106862,RMVar_hsa_circ_239994,RMVar_hsa_circ_64770,RMVar_hsa_circ_239999,RMVar_hsa_circ_12386,RMVar_hsa_circ_240000,RMVar_hsa_circ_67267 49830 RMVar_ID_49830 Human_SNP_ID_285505037 A-to-I Human chr6 - 85515183 85515183 85515183 GGCTCACTGTTACCTCTGGCTCCCAGGTTCAAACTATTCTCCTGCCTCAGTCTCCCAAGTAGCTG GGCTCACTGTTACCTCTGGCTCCCAGGTTCAAGCTATTCTCCTGCCTCAGTCTCCCAAGTAGCTG T C SNX14 Ensembl:ENSG00000135317 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1562194741 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15895349 RMVar_hsa_circ_788,RMVar_hsa_circ_276806,RMVar_hsa_circ_319549,RMVar_hsa_circ_327319,RMVar_hsa_circ_350893,RMVar_hsa_circ_331773,RMVar_hsa_circ_313890,RMVar_hsa_circ_316419,RMVar_hsa_circ_287418,RMVar_hsa_circ_102147,RMVar_hsa_circ_49241,RMVar_hsa_circ_35029,RMVar_hsa_circ_37864,RMVar_hsa_circ_239988,RMVar_hsa_circ_239990,RMVar_hsa_circ_239992,RMVar_hsa_circ_239993,RMVar_hsa_circ_239991,RMVar_hsa_circ_239989,RMVar_hsa_circ_361057,RMVar_hsa_circ_55344,RMVar_hsa_circ_109809,RMVar_hsa_circ_324423,RMVar_hsa_circ_345569,RMVar_hsa_circ_275106,RMVar_hsa_circ_49914,RMVar_hsa_circ_239995,RMVar_hsa_circ_239997,RMVar_hsa_circ_14651,RMVar_hsa_circ_239996,RMVar_hsa_circ_106862,RMVar_hsa_circ_239994,RMVar_hsa_circ_64770,RMVar_hsa_circ_239999,RMVar_hsa_circ_12386,RMVar_hsa_circ_240000,RMVar_hsa_circ_67267 49831 RMVar_ID_49831 Human_SNP_ID_285512379 A-to-I Human chr6 - 85545857 85545857 85545857 GCAACATAGTGAAACCCTGTCTCGACAAAAATACAAAAATTAGCTGGGCGTGTTGGCTCATGCCT GCAACATAGTGAAACCCTGTCTCGACAAAAATTCAAAAATTAGCTGGGCGTGTTGGCTCATGCCT T A SNX14 Ensembl:ENSG00000135317 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs751467570 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_788,RMVar_hsa_circ_327319,RMVar_hsa_circ_350893,RMVar_hsa_circ_313890,RMVar_hsa_circ_49241,RMVar_hsa_circ_37864,RMVar_hsa_circ_239992,RMVar_hsa_circ_239993,RMVar_hsa_circ_324423,RMVar_hsa_circ_345569,RMVar_hsa_circ_275106,RMVar_hsa_circ_49914,RMVar_hsa_circ_239995,RMVar_hsa_circ_14651,RMVar_hsa_circ_239996,RMVar_hsa_circ_106862,RMVar_hsa_circ_239994,RMVar_hsa_circ_64770,RMVar_hsa_circ_239999,RMVar_hsa_circ_240000,RMVar_hsa_circ_350408,RMVar_hsa_circ_353121,RMVar_hsa_circ_1167,RMVar_hsa_circ_59892,RMVar_hsa_circ_57500,RMVar_hsa_circ_82948,RMVar_hsa_circ_1617,RMVar_hsa_circ_34980,RMVar_hsa_circ_347011,RMVar_hsa_circ_240006,RMVar_hsa_circ_95084,RMVar_hsa_circ_313051,RMVar_hsa_circ_38555,RMVar_hsa_circ_240007,RMVar_hsa_circ_99100,RMVar_hsa_circ_240016,RMVar_hsa_circ_61969,RMVar_hsa_circ_240020,RMVar_hsa_circ_349525,RMVar_hsa_circ_62747,RMVar_hsa_circ_325332,RMVar_hsa_circ_69223,RMVar_hsa_circ_326002,RMVar_hsa_circ_69738,RMVar_hsa_circ_240023,RMVar_hsa_circ_2316,RMVar_hsa_circ_83693,RMVar_hsa_circ_361901,RMVar_hsa_circ_240024,RMVar_hsa_circ_359728,RMVar_hsa_circ_338551,RMVar_hsa_circ_47958,RMVar_hsa_circ_67947,RMVar_hsa_circ_44910,RMVar_hsa_circ_308852,RMVar_hsa_circ_240026,RMVar_hsa_circ_240027,RMVar_hsa_circ_348436,RMVar_hsa_circ_359926,RMVar_hsa_circ_314260,RMVar_hsa_circ_324482,RMVar_hsa_circ_313512,RMVar_hsa_circ_283904,RMVar_hsa_circ_299324,RMVar_hsa_circ_37788,RMVar_hsa_circ_240031,RMVar_hsa_circ_240033,RMVar_hsa_circ_240034,RMVar_hsa_circ_240032,RMVar_hsa_circ_240029,RMVar_hsa_circ_240030,RMVar_hsa_circ_240028,RMVar_hsa_circ_356347,RMVar_hsa_circ_13893,RMVar_hsa_circ_30039,RMVar_hsa_circ_59943,RMVar_hsa_circ_26134,RMVar_hsa_circ_240036 49832 RMVar_ID_49832 Human_SNP_ID_285512388 A-to-I Human chr6 - 85545882 85545882 85545882 AGTCAGGAGTTCGAGACCAACCTGGGCAACATAGTGAAACCCTGTCTCGACAAAAATACAAAAAT AGTCAGGAGTTCGAGACCAACCTGGGCAACATGGTGAAACCCTGTCTCGACAAAAATACAAAAAT T C SNX14 Ensembl:ENSG00000135317 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1372368470 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_788,RMVar_hsa_circ_327319,RMVar_hsa_circ_350893,RMVar_hsa_circ_313890,RMVar_hsa_circ_49241,RMVar_hsa_circ_37864,RMVar_hsa_circ_239992,RMVar_hsa_circ_239993,RMVar_hsa_circ_324423,RMVar_hsa_circ_345569,RMVar_hsa_circ_275106,RMVar_hsa_circ_49914,RMVar_hsa_circ_239995,RMVar_hsa_circ_14651,RMVar_hsa_circ_239996,RMVar_hsa_circ_106862,RMVar_hsa_circ_239994,RMVar_hsa_circ_64770,RMVar_hsa_circ_239999,RMVar_hsa_circ_240000,RMVar_hsa_circ_350408,RMVar_hsa_circ_353121,RMVar_hsa_circ_1167,RMVar_hsa_circ_59892,RMVar_hsa_circ_57500,RMVar_hsa_circ_82948,RMVar_hsa_circ_1617,RMVar_hsa_circ_34980,RMVar_hsa_circ_347011,RMVar_hsa_circ_240006,RMVar_hsa_circ_95084,RMVar_hsa_circ_313051,RMVar_hsa_circ_38555,RMVar_hsa_circ_240007,RMVar_hsa_circ_99100,RMVar_hsa_circ_240016,RMVar_hsa_circ_61969,RMVar_hsa_circ_240020,RMVar_hsa_circ_349525,RMVar_hsa_circ_62747,RMVar_hsa_circ_325332,RMVar_hsa_circ_69223,RMVar_hsa_circ_326002,RMVar_hsa_circ_69738,RMVar_hsa_circ_240023,RMVar_hsa_circ_2316,RMVar_hsa_circ_83693,RMVar_hsa_circ_361901,RMVar_hsa_circ_240024,RMVar_hsa_circ_359728,RMVar_hsa_circ_338551,RMVar_hsa_circ_47958,RMVar_hsa_circ_67947,RMVar_hsa_circ_44910,RMVar_hsa_circ_308852,RMVar_hsa_circ_240026,RMVar_hsa_circ_240027,RMVar_hsa_circ_348436,RMVar_hsa_circ_359926,RMVar_hsa_circ_314260,RMVar_hsa_circ_324482,RMVar_hsa_circ_313512,RMVar_hsa_circ_283904,RMVar_hsa_circ_299324,RMVar_hsa_circ_37788,RMVar_hsa_circ_240031,RMVar_hsa_circ_240033,RMVar_hsa_circ_240034,RMVar_hsa_circ_240032,RMVar_hsa_circ_240029,RMVar_hsa_circ_240030,RMVar_hsa_circ_240028,RMVar_hsa_circ_356347,RMVar_hsa_circ_13893,RMVar_hsa_circ_30039,RMVar_hsa_circ_59943,RMVar_hsa_circ_26134,RMVar_hsa_circ_240036 49833 RMVar_ID_49833 Human_SNP_ID_285512398 A-to-I Human chr6 - 85545929 85545929 85545929 CTTACAATCCCAGCACTTCGGGAGGCCGAGGCAGGTGGATCACTTGAAGTCAGGAGTTCGAGACC CTTACAATCCCAGCACTTCGGGAGGCCGAGGCGGGTGGATCACTTGAAGTCAGGAGTTCGAGACC T C SNX14 Ensembl:ENSG00000135317 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1217857068 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_788,RMVar_hsa_circ_327319,RMVar_hsa_circ_350893,RMVar_hsa_circ_313890,RMVar_hsa_circ_49241,RMVar_hsa_circ_37864,RMVar_hsa_circ_239992,RMVar_hsa_circ_239993,RMVar_hsa_circ_324423,RMVar_hsa_circ_345569,RMVar_hsa_circ_275106,RMVar_hsa_circ_49914,RMVar_hsa_circ_239995,RMVar_hsa_circ_14651,RMVar_hsa_circ_239996,RMVar_hsa_circ_106862,RMVar_hsa_circ_239994,RMVar_hsa_circ_64770,RMVar_hsa_circ_239999,RMVar_hsa_circ_240000,RMVar_hsa_circ_350408,RMVar_hsa_circ_353121,RMVar_hsa_circ_1167,RMVar_hsa_circ_59892,RMVar_hsa_circ_57500,RMVar_hsa_circ_82948,RMVar_hsa_circ_1617,RMVar_hsa_circ_34980,RMVar_hsa_circ_347011,RMVar_hsa_circ_240006,RMVar_hsa_circ_95084,RMVar_hsa_circ_313051,RMVar_hsa_circ_38555,RMVar_hsa_circ_240007,RMVar_hsa_circ_99100,RMVar_hsa_circ_240016,RMVar_hsa_circ_61969,RMVar_hsa_circ_240020,RMVar_hsa_circ_349525,RMVar_hsa_circ_62747,RMVar_hsa_circ_325332,RMVar_hsa_circ_69223,RMVar_hsa_circ_326002,RMVar_hsa_circ_69738,RMVar_hsa_circ_240023,RMVar_hsa_circ_2316,RMVar_hsa_circ_83693,RMVar_hsa_circ_361901,RMVar_hsa_circ_240024,RMVar_hsa_circ_359728,RMVar_hsa_circ_338551,RMVar_hsa_circ_47958,RMVar_hsa_circ_67947,RMVar_hsa_circ_44910,RMVar_hsa_circ_308852,RMVar_hsa_circ_240026,RMVar_hsa_circ_240027,RMVar_hsa_circ_348436,RMVar_hsa_circ_359926,RMVar_hsa_circ_314260,RMVar_hsa_circ_324482,RMVar_hsa_circ_313512,RMVar_hsa_circ_283904,RMVar_hsa_circ_299324,RMVar_hsa_circ_37788,RMVar_hsa_circ_240031,RMVar_hsa_circ_240033,RMVar_hsa_circ_240034,RMVar_hsa_circ_240032,RMVar_hsa_circ_240029,RMVar_hsa_circ_240030,RMVar_hsa_circ_240028,RMVar_hsa_circ_356347,RMVar_hsa_circ_13893,RMVar_hsa_circ_30039,RMVar_hsa_circ_59943,RMVar_hsa_circ_26134,RMVar_hsa_circ_240036 49834 RMVar_ID_49834 Human_SNP_ID_285513484 A-to-I Human chr6 - 85550006 85550006 85550006 CTGGCCTCAAGCGATTTGCCTGCCTCGGCCTCACAAAATGCTGGGATTACAGGCATGAGCCACCA CTGGCCTCAAGCGATTTGCCTGCCTCGGCCTCCCAAAATGCTGGGATTACAGGCATGAGCCACCA T G SNX14 Ensembl:ENSG00000135317 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs573291804 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10301994 RMVar_hsa_circ_788,RMVar_hsa_circ_327319,RMVar_hsa_circ_350893,RMVar_hsa_circ_313890,RMVar_hsa_circ_49241,RMVar_hsa_circ_239992,RMVar_hsa_circ_239993,RMVar_hsa_circ_324423,RMVar_hsa_circ_275106,RMVar_hsa_circ_239995,RMVar_hsa_circ_14651,RMVar_hsa_circ_106862,RMVar_hsa_circ_239994,RMVar_hsa_circ_64770,RMVar_hsa_circ_239999,RMVar_hsa_circ_240000,RMVar_hsa_circ_350408,RMVar_hsa_circ_353121,RMVar_hsa_circ_1167,RMVar_hsa_circ_1617,RMVar_hsa_circ_34980,RMVar_hsa_circ_347011,RMVar_hsa_circ_313051,RMVar_hsa_circ_240007,RMVar_hsa_circ_99100,RMVar_hsa_circ_240016,RMVar_hsa_circ_61969,RMVar_hsa_circ_240020,RMVar_hsa_circ_349525,RMVar_hsa_circ_62747,RMVar_hsa_circ_325332,RMVar_hsa_circ_69223,RMVar_hsa_circ_326002,RMVar_hsa_circ_240023,RMVar_hsa_circ_2316,RMVar_hsa_circ_83693,RMVar_hsa_circ_240024,RMVar_hsa_circ_359728,RMVar_hsa_circ_338551,RMVar_hsa_circ_47958,RMVar_hsa_circ_44910,RMVar_hsa_circ_308852,RMVar_hsa_circ_240026,RMVar_hsa_circ_240027,RMVar_hsa_circ_314260,RMVar_hsa_circ_324482,RMVar_hsa_circ_313512,RMVar_hsa_circ_283904,RMVar_hsa_circ_299324,RMVar_hsa_circ_37788,RMVar_hsa_circ_240031,RMVar_hsa_circ_240033,RMVar_hsa_circ_240032,RMVar_hsa_circ_240029,RMVar_hsa_circ_240030,RMVar_hsa_circ_240028,RMVar_hsa_circ_356347,RMVar_hsa_circ_13893,RMVar_hsa_circ_26134,RMVar_hsa_circ_24777,RMVar_hsa_circ_66777,RMVar_hsa_circ_312949,RMVar_hsa_circ_334006,RMVar_hsa_circ_293498,RMVar_hsa_circ_240040,RMVar_hsa_circ_240042,RMVar_hsa_circ_86642,RMVar_hsa_circ_240041,RMVar_hsa_circ_240039,RMVar_hsa_circ_28339,RMVar_hsa_circ_10141,RMVar_hsa_circ_240043,RMVar_hsa_circ_240044,RMVar_hsa_circ_334822,RMVar_hsa_circ_281442,RMVar_hsa_circ_312428 49835 RMVar_ID_49835 Human_SNP_ID_285514865 A-to-I Human chr6 - 85555949 85555949 85555949 AGTTTCGCTCTAGTTGCCCAGTCTGGAGACCAATGGCACAATCTCAGCTCACTGCAACCTCCACT AGTTTCGCTCTAGTTGCCCAGTCTGGAGACCAGTGGCACAATCTCAGCTCACTGCAACCTCCACT T C SNX14 Ensembl:ENSG00000135317 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1480389251 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_788,RMVar_hsa_circ_327319,RMVar_hsa_circ_350893,RMVar_hsa_circ_313890,RMVar_hsa_circ_49241,RMVar_hsa_circ_239992,RMVar_hsa_circ_239993,RMVar_hsa_circ_324423,RMVar_hsa_circ_275106,RMVar_hsa_circ_239995,RMVar_hsa_circ_14651,RMVar_hsa_circ_106862,RMVar_hsa_circ_239994,RMVar_hsa_circ_64770,RMVar_hsa_circ_239999,RMVar_hsa_circ_240000,RMVar_hsa_circ_350408,RMVar_hsa_circ_353121,RMVar_hsa_circ_1167,RMVar_hsa_circ_1617,RMVar_hsa_circ_34980,RMVar_hsa_circ_347011,RMVar_hsa_circ_313051,RMVar_hsa_circ_240007,RMVar_hsa_circ_99100,RMVar_hsa_circ_240016,RMVar_hsa_circ_61969,RMVar_hsa_circ_240020,RMVar_hsa_circ_349525,RMVar_hsa_circ_62747,RMVar_hsa_circ_325332,RMVar_hsa_circ_69223,RMVar_hsa_circ_326002,RMVar_hsa_circ_240023,RMVar_hsa_circ_2316,RMVar_hsa_circ_83693,RMVar_hsa_circ_240024,RMVar_hsa_circ_359728,RMVar_hsa_circ_338551,RMVar_hsa_circ_47958,RMVar_hsa_circ_44910,RMVar_hsa_circ_308852,RMVar_hsa_circ_240026,RMVar_hsa_circ_240027,RMVar_hsa_circ_314260,RMVar_hsa_circ_324482,RMVar_hsa_circ_313512,RMVar_hsa_circ_283904,RMVar_hsa_circ_299324,RMVar_hsa_circ_37788,RMVar_hsa_circ_240031,RMVar_hsa_circ_240033,RMVar_hsa_circ_240032,RMVar_hsa_circ_240029,RMVar_hsa_circ_240030,RMVar_hsa_circ_240028,RMVar_hsa_circ_356347,RMVar_hsa_circ_13893,RMVar_hsa_circ_26134,RMVar_hsa_circ_24777,RMVar_hsa_circ_66777,RMVar_hsa_circ_312949,RMVar_hsa_circ_334006,RMVar_hsa_circ_293498,RMVar_hsa_circ_240040,RMVar_hsa_circ_240042,RMVar_hsa_circ_86642,RMVar_hsa_circ_240041,RMVar_hsa_circ_240039,RMVar_hsa_circ_28339,RMVar_hsa_circ_10141,RMVar_hsa_circ_240043,RMVar_hsa_circ_240044,RMVar_hsa_circ_334822,RMVar_hsa_circ_281442,RMVar_hsa_circ_312428 49836 RMVar_ID_49836 Human_SNP_ID_285516626 A-to-I Human chr6 - 85563572 85563572 85563572 CCTGGCCAACATGGTGAAACTCTGTCTCTACTAAAAATACAAAAAATTAGCCAGGCATGGGGGCG CCTGGCCAACATGGTGAAACTCTGTCTCTACTGAAAATACAAAAAATTAGCCAGGCATGGGGGCG T C SNX14,AL589666.1 Ensembl:ENSG00000135317,Ensembl:ENSG00000271793 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs774364533 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_788,RMVar_hsa_circ_327319,RMVar_hsa_circ_313890,RMVar_hsa_circ_49241,RMVar_hsa_circ_239992,RMVar_hsa_circ_239993,RMVar_hsa_circ_275106,RMVar_hsa_circ_14651,RMVar_hsa_circ_106862,RMVar_hsa_circ_239994,RMVar_hsa_circ_240000,RMVar_hsa_circ_350408,RMVar_hsa_circ_1167,RMVar_hsa_circ_313051,RMVar_hsa_circ_240007,RMVar_hsa_circ_99100,RMVar_hsa_circ_240016,RMVar_hsa_circ_61969,RMVar_hsa_circ_62747,RMVar_hsa_circ_325332,RMVar_hsa_circ_69223,RMVar_hsa_circ_2316,RMVar_hsa_circ_83693,RMVar_hsa_circ_240024,RMVar_hsa_circ_359728,RMVar_hsa_circ_47958,RMVar_hsa_circ_44910,RMVar_hsa_circ_308852,RMVar_hsa_circ_240027,RMVar_hsa_circ_324482,RMVar_hsa_circ_313512,RMVar_hsa_circ_283904,RMVar_hsa_circ_299324,RMVar_hsa_circ_37788,RMVar_hsa_circ_240031,RMVar_hsa_circ_240032,RMVar_hsa_circ_240029,RMVar_hsa_circ_240030,RMVar_hsa_circ_240028,RMVar_hsa_circ_13893,RMVar_hsa_circ_26134,RMVar_hsa_circ_24777,RMVar_hsa_circ_312949,RMVar_hsa_circ_293498,RMVar_hsa_circ_240040,RMVar_hsa_circ_240042,RMVar_hsa_circ_86642,RMVar_hsa_circ_240041,RMVar_hsa_circ_240046,RMVar_hsa_circ_240050,RMVar_hsa_circ_273516,RMVar_hsa_circ_28339,RMVar_hsa_circ_10141,RMVar_hsa_circ_240043,RMVar_hsa_circ_240044,RMVar_hsa_circ_334822,RMVar_hsa_circ_317757,RMVar_hsa_circ_324669,RMVar_hsa_circ_287691,RMVar_hsa_circ_272076,RMVar_hsa_circ_272175,RMVar_hsa_circ_240051,RMVar_hsa_circ_240048,RMVar_hsa_circ_240049,RMVar_hsa_circ_240047,RMVar_hsa_circ_240045 49837 RMVar_ID_49837 Human_SNP_ID_285517707 A-to-I Human chr6 - 85567926 85567926 85567926 CAGGCTGGTGTACAGTGGCAACATCTTGGCTCACTGTAACCTCTGCCTCTCAGGCTCAAGCGATA CAGGCTGGTGTACAGTGGCAACATCTTGGCTCGCTGTAACCTCTGCCTCTCAGGCTCAAGCGATA T C SNX14,AL589666.1 Ensembl:ENSG00000135317,Ensembl:ENSG00000271793 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1197928113 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8650574,Human_RBP_ID_15895845 RMVar_hsa_circ_788,RMVar_hsa_circ_327319,RMVar_hsa_circ_49241,RMVar_hsa_circ_239993,RMVar_hsa_circ_275106,RMVar_hsa_circ_14651,RMVar_hsa_circ_106862,RMVar_hsa_circ_239994,RMVar_hsa_circ_240000,RMVar_hsa_circ_313051,RMVar_hsa_circ_240007,RMVar_hsa_circ_99100,RMVar_hsa_circ_240016,RMVar_hsa_circ_61969,RMVar_hsa_circ_325332,RMVar_hsa_circ_2316,RMVar_hsa_circ_83693,RMVar_hsa_circ_240024,RMVar_hsa_circ_359728,RMVar_hsa_circ_44910,RMVar_hsa_circ_308852,RMVar_hsa_circ_240027,RMVar_hsa_circ_324482,RMVar_hsa_circ_299324,RMVar_hsa_circ_37788,RMVar_hsa_circ_240029,RMVar_hsa_circ_240030,RMVar_hsa_circ_240028,RMVar_hsa_circ_26134,RMVar_hsa_circ_312949,RMVar_hsa_circ_240042,RMVar_hsa_circ_86642,RMVar_hsa_circ_240041,RMVar_hsa_circ_240050,RMVar_hsa_circ_10141,RMVar_hsa_circ_240043,RMVar_hsa_circ_240044,RMVar_hsa_circ_334822,RMVar_hsa_circ_317757,RMVar_hsa_circ_324669,RMVar_hsa_circ_287691,RMVar_hsa_circ_272175,RMVar_hsa_circ_240051,RMVar_hsa_circ_240048,RMVar_hsa_circ_240049,RMVar_hsa_circ_240047,RMVar_hsa_circ_240053,RMVar_hsa_circ_291621,RMVar_hsa_circ_312652,RMVar_hsa_circ_291813,RMVar_hsa_circ_240055,RMVar_hsa_circ_240056,RMVar_hsa_circ_240054,RMVar_hsa_circ_240057,RMVar_hsa_circ_240052,RMVar_hsa_circ_303202 49838 RMVar_ID_49838 Human_SNP_ID_285522478 A-to-I Human chr6 - 85588220 85588220 85588220 GCTAGACAGTGGCATGATCTTGGCTCACTGCAACCTCCACCTCATGGGCTCAAGCAGTCCTCCCA GCTAGACAGTGGCATGATCTTGGCTCACTGCATCCTCCACCTCATGGGCTCAAGCAGTCCTCCCA T A SNX14,AL589666.1 Ensembl:ENSG00000135317,Ensembl:ENSG00000271793 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1451237836 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83693,RMVar_hsa_circ_240027,RMVar_hsa_circ_240052,RMVar_hsa_circ_240062 49839 RMVar_ID_49839 Human_SNP_ID_285529999 A-to-I Human chr6 - 85615748 85615748 85615748 TGGAGTGCAGTGATGTGACCTTGGCTTACTGCAGCCTCCGCCACCTGGGTTCAAGCGATTCACCT TGGAGTGCAGTGATGTGACCTTGGCTTACTGCGGCCTCCGCCACCTGGGTTCAAGCGATTCACCT T C SYNCRIP Ensembl:ENSG00000135316 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs577443822 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15896793 RMVar_hsa_circ_9479,RMVar_hsa_circ_240063 49840 RMVar_ID_49840 Human_SNP_ID_285530211 A-to-I Human chr6 - 85616466 85616466 85616466 TAAAAATTGGCTAGGTATGGTGGCACATGCCTATAGTCCCAGCTACTCGAGAGGCTGTGGCAGGA TAAAAATTGGCTAGGTATGGTGGCACATGCCTGTAGTCCCAGCTACTCGAGAGGCTGTGGCAGGA T C SYNCRIP Ensembl:ENSG00000135316 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1258544366 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9479,RMVar_hsa_circ_240063 49841 RMVar_ID_49841 Human_SNP_ID_285535505 A-to-I Human chr6 - 85633903 85633903 85633903 TAAAAGATACTTTTGGCAGGGTGTGGTTGCTCACACCTGTAGTCCCAGCACTTTGGTAGGCTGAG TAAAAGATACTTTTGGCAGGGTGTGGTTGCTCGCACCTGTAGTCCCAGCACTTTGGTAGGCTGAG T C SYNCRIP Ensembl:ENSG00000135316 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1052144244 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_790293,Human_RBP_ID_10302549,Human_RBP_ID_15897596 RMVar_hsa_circ_9479,RMVar_hsa_circ_240063,RMVar_hsa_circ_284713,RMVar_hsa_circ_359214,RMVar_hsa_circ_240067,RMVar_hsa_circ_304731,RMVar_hsa_circ_83165 49842 RMVar_ID_49842 Human_SNP_ID_285535886 A-to-I Human chr6 - 85635078 85635078 85635078 TCACTGTAATCTCTGCCTCCTGGGCTCAGGCAATTCTCCTGCCTCAGCCACCCGAGTAGCTGGGA TCACTGTAATCTCTGCCTCCTGGGCTCAGGCAGTTCTCCTGCCTCAGCCACCCGAGTAGCTGGGA T C SYNCRIP Ensembl:ENSG00000135316 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs962941151 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8650688,Human_RBP_ID_15897686 RMVar_hsa_circ_9479,RMVar_hsa_circ_240063,RMVar_hsa_circ_284713,RMVar_hsa_circ_359214,RMVar_hsa_circ_240067,RMVar_hsa_circ_304731,RMVar_hsa_circ_83165 49843 RMVar_ID_49843 Human_SNP_ID_285535917 A-to-I Human chr6 - 85635154 85635154 85635154 TAGTTTGTTTTTATGATTTGTTTTTTGAGACAAAGTCTCTGTCACCCACGCTGGAGTGTGTGGGC TAGTTTGTTTTTATGATTTGTTTTTTGAGACAGAGTCTCTGTCACCCACGCTGGAGTGTGTGGGC T C SYNCRIP Ensembl:ENSG00000135316 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946384324 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3022679,Human_RBP_ID_7665383,Human_RBP_ID_15897686 RMVar_hsa_circ_9479,RMVar_hsa_circ_240063,RMVar_hsa_circ_284713,RMVar_hsa_circ_359214,RMVar_hsa_circ_240067,RMVar_hsa_circ_304731,RMVar_hsa_circ_83165 49844 RMVar_ID_49844 Human_SNP_ID_285546416 A-to-I Human chr6 - 85672983 85672983 85672983 GAACACACCTTGCTATTGCCCTAGAGAAGTTTAATGTGTTTTATGCCTATGTTCCTATTGATGCA GAACACACCTTGCTATTGCCCTAGAGAAGTTTTATGTGTTTTATGCCTATGTTCCTATTGATGCA T A SNHG5 Ensembl:ENSG00000203875 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1271505532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8271125 49845 RMVar_ID_49845 Human_SNP_ID_285546417 A-to-I Human chr6 - 85672983 85672983 85672983 GAACACACCTTGCTATTGCCCTAGAGAAGTTTAATGTGTTTTATGCCTATGTTCCTATTGATGCA GAACACACCTTGCTATTGCCCTAGAGAAGTTTGATGTGTTTTATGCCTATGTTCCTATTGATGCA T C SNHG5 Ensembl:ENSG00000203875 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1271505532 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8271125 49846 RMVar_ID_49846 Human_SNP_ID_285549132 A-to-I Human chr6 + 85681324 85681324 85681324 CAGATGGGCCGGGCGTGGTGGTTCATGCCTGTAAGCCCAGCACTTTGGGAAGCCAAAACGGGTGG CAGATGGGCCGGGCGTGGTGGTTCATGCCTGTGAGCCCAGCACTTTGGGAAGCCAAAACGGGTGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388079051 Functional Loss SNV dbSNP153 33..33 33 - - - 49847 RMVar_ID_49847 Human_SNP_ID_285704873 A-to-I Human chr6 - 86170643 86170643 86170643 GATTGCCCACAAAGAAAGTAGACTACACAACAACAAAGGAATTTGCTGATTCCCTTGGAATTCCA GATTGCCCACAAAGAAAGTAGACTACACAACATCAAAGGAATTTGCTGATTCCCTTGGAATTCCA T A RAB1AP2 Ensembl:ENSG00000217272 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs548074429 Functional Loss SNV dbSNP153 33..33 33 - - - 49848 RMVar_ID_49848 Human_SNP_ID_286000859 A-to-I Human chr6 - 87122443 87122443 87122443 ACTCTAAGACCTTCGACCAGCTCACCCCGGACAAGAGCAAGGAGAGGCTGGGGAAGATTGTTGAT ACTCTAAGACCTTCGACCAGCTCACCCCGGACGAGAGCAAGGAGAGGCTGGGGAAGATTGTTGAT T C RCN1P1 Ensembl:ENSG00000215477 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1447538614 Functional Loss SNV dbSNP153 33..33 33 - - - 49849 RMVar_ID_49849 Human_SNP_ID_286014344 A-to-I Human chr6 + 87167546 87167546 87167546 GCCTGTAATCCCAGCTACCTGGGAGGCTGAGCAAGGAGAATCACTTGAACTAGGGAGGTGGAGGT GCCTGTAATCCCAGCTACCTGGGAGGCTGAGCCAGGAGAATCACTTGAACTAGGGAGGTGGAGGT A C ZNF292 Ensembl:ENSG00000188994 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1034901077 Functional Loss SNV dbSNP153 33..33 33 - - - 49850 RMVar_ID_49850 Human_SNP_ID_286023453 A-to-I Human chr6 + 87203395 87203395 87203395 GGACTTCTGAGCTTAAGTGATCCACCCGCCTCAGCCTACCAAAGTGCTGGGATTACAAGTGTGAG GGACTTCTGAGCTTAAGTGATCCACCCGCCTCCGCCTACCAAAGTGCTGGGATTACAAGTGTGAG A C ZNF292 Ensembl:ENSG00000188994 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1240228091 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15899641 49851 RMVar_ID_49851 Human_SNP_ID_286029793 A-to-I Human chr6 + 87229470 87229470 87229470 TTTTTGAGACGGAGTTTTTGCTCTTGTTGCCCAGGCTGGAGTGCAATGGCGCAATCTCGGCTAAC TTTTTGAGACGGAGTTTTTGCTCTTGTTGCCCGGGCTGGAGTGCAATGGCGCAATCTCGGCTAAC A G ZNF292 Ensembl:ENSG00000188994 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1273154582 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_240095,RMVar_hsa_circ_32619,RMVar_hsa_circ_240091,RMVar_hsa_circ_64520,RMVar_hsa_circ_307182,RMVar_hsa_circ_330120,RMVar_hsa_circ_271732,RMVar_hsa_circ_98472,RMVar_hsa_circ_240093,RMVar_hsa_circ_240094,RMVar_hsa_circ_104070,RMVar_hsa_circ_240099,RMVar_hsa_circ_240101 49852 RMVar_ID_49852 Human_SNP_ID_286029838 A-to-I Human chr6 + 87229606 87229605 87229606 GCGCCTCCACGCCCAGCTAATTTTGTATTTTTAGTAGAGACACGGTTTCTCCATGTTGGTCAGGC GCGCCTCCACGCCCAGCTAATTTTGTATTTTT_GTAGAGACACGGTTTCTCCATGTTGGTCAGGC TA T ZNF292 Ensembl:ENSG00000188994 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1205024335 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_240095,RMVar_hsa_circ_32619,RMVar_hsa_circ_240091,RMVar_hsa_circ_64520,RMVar_hsa_circ_307182,RMVar_hsa_circ_330120,RMVar_hsa_circ_271732,RMVar_hsa_circ_98472,RMVar_hsa_circ_240093,RMVar_hsa_circ_240094,RMVar_hsa_circ_104070,RMVar_hsa_circ_240099,RMVar_hsa_circ_240101 49853 RMVar_ID_49853 Human_SNP_ID_286033010 A-to-I Human chr6 + 87240601 87240601 87240601 CTGCTACCATGCCTGGCTAATTTTGTATTTTTAGTAGAGACAGGGTTTCACTATGTTGGTCAGGC CTGCTACCATGCCTGGCTAATTTTGTATTTTTGGTAGAGACAGGGTTTCACTATGTTGGTCAGGC A G ZNF292 Ensembl:ENSG00000188994 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1268054119 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32619,RMVar_hsa_circ_240091,RMVar_hsa_circ_307182,RMVar_hsa_circ_330120,RMVar_hsa_circ_98472,RMVar_hsa_circ_240093,RMVar_hsa_circ_240094,RMVar_hsa_circ_104070,RMVar_hsa_circ_240099,RMVar_hsa_circ_240101,RMVar_hsa_circ_58973,RMVar_hsa_circ_240103 49854 RMVar_ID_49854 Human_SNP_ID_286033012 A-to-I Human chr6 + 87240610 87240609 87240611 TGCCTGGCTAATTTTGTATTTTTAGTAGAGACAGGGTTTCACTATGTTGGTCAGGCTGGTCTCGA TGCCTGGCTAATTTTGTATTTTTAGTAGAGAC__GGTTTCACTATGTTGGTCAGGCTGGTCTCGA CAG C ZNF292 Ensembl:ENSG00000188994 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1376119491 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_26030035 RMVar_hsa_circ_32619,RMVar_hsa_circ_240091,RMVar_hsa_circ_307182,RMVar_hsa_circ_330120,RMVar_hsa_circ_98472,RMVar_hsa_circ_240093,RMVar_hsa_circ_240094,RMVar_hsa_circ_104070,RMVar_hsa_circ_240099,RMVar_hsa_circ_240101,RMVar_hsa_circ_58973,RMVar_hsa_circ_240103 49855 RMVar_ID_49855 Human_SNP_ID_286033014 A-to-I Human chr6 + 87240621 87240621 87240621 TTTTGTATTTTTAGTAGAGACAGGGTTTCACTATGTTGGTCAGGCTGGTCTCGAACTCCTGACCT TTTTGTATTTTTAGTAGAGACAGGGTTTCACTGTGTTGGTCAGGCTGGTCTCGAACTCCTGACCT A G ZNF292 Ensembl:ENSG00000188994 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs112764154 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32619,RMVar_hsa_circ_240091,RMVar_hsa_circ_307182,RMVar_hsa_circ_330120,RMVar_hsa_circ_98472,RMVar_hsa_circ_240093,RMVar_hsa_circ_240094,RMVar_hsa_circ_104070,RMVar_hsa_circ_240099,RMVar_hsa_circ_240101,RMVar_hsa_circ_58973,RMVar_hsa_circ_240103 49856 RMVar_ID_49856 Human_SNP_ID_286033310 A-to-I Human chr6 + 87241603 87241603 87241603 ACCATGTCCAGCTAGTTTTTGTATGTTTTAGTAGAGATGGGATTTCACCATGTTGGCCAGGCTGG ACCATGTCCAGCTAGTTTTTGTATGTTTTAGTGGAGATGGGATTTCACCATGTTGGCCAGGCTGG A G ZNF292 Ensembl:ENSG00000188994 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1434204710 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_32619,RMVar_hsa_circ_240091,RMVar_hsa_circ_307182,RMVar_hsa_circ_330120,RMVar_hsa_circ_98472,RMVar_hsa_circ_240093,RMVar_hsa_circ_240094,RMVar_hsa_circ_104070,RMVar_hsa_circ_240099,RMVar_hsa_circ_240101,RMVar_hsa_circ_58973,RMVar_hsa_circ_240103 49857 RMVar_ID_49857 Human_SNP_ID_286035304 A-to-I Human chr6 + 87249310 87249310 87249310 CATCACACTTGGCTAATTTTTTTATTTTTTGTAGAGATGGGGTCTCACTATATTGCCCAGATTTA CATCACACTTGGCTAATTTTTTTATTTTTTGTGGAGATGGGGTCTCACTATATTGCCCAGATTTA A G ZNF292 Ensembl:ENSG00000188994 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1173120066 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104070,RMVar_hsa_circ_240101,RMVar_hsa_circ_240103 49858 RMVar_ID_49858 Human_SNP_ID_286035312 A-to-I Human chr6 + 87249329 87249329 87249329 TTTTATTTTTTGTAGAGATGGGGTCTCACTATATTGCCCAGATTTATCTCCAACTCCTGGGCTCA TTTTATTTTTTGTAGAGATGGGGTCTCACTATGTTGCCCAGATTTATCTCCAACTCCTGGGCTCA A G ZNF292 Ensembl:ENSG00000188994 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs535961587 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_793682 RMVar_hsa_circ_104070,RMVar_hsa_circ_240101,RMVar_hsa_circ_240103 49859 RMVar_ID_49859 Human_SNP_ID_286035480 A-to-I Human chr6 + 87249875 87249875 87249875 AGGATTACAGGCGGACGCCACCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTTA AGGATTACAGGCGGACGCCACCATGCCCAGCTGATTTTTGTATTTTTAGTAGAGACAGGGTTTTA A G ZNF292 Ensembl:ENSG00000188994 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1479191710 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104070,RMVar_hsa_circ_240101,RMVar_hsa_circ_240103 49860 RMVar_ID_49860 Human_SNP_ID_286040082 A-to-I Human chr6 + 87265214 87265214 87265214 TCGGCTTACTGCAACTTCTGCCTCCCAAGTTCAAGTGATTCTCCTGCCTCAGCCTCCCCAGTAGC TCGGCTTACTGCAACTTCTGCCTCCCAAGTTCGAGTGATTCTCCTGCCTCAGCCTCCCCAGTAGC A G ZNF292 Ensembl:ENSG00000188994 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1410953326 Functional Loss SNV dbSNP153 33..33 33 - - - 49861 RMVar_ID_49861 Human_SNP_ID_286057854 A-to-I Human chr6 + 87337799 87337799 87337799 CAGGTGCACGCCTTTATGCCTGGCTCATTTTTAAAATTTTTTGTAGAGATGGTGTGTCAGTATAT CAGGTGCACGCCTTTATGCCTGGCTCATTTTTTAAATTTTTTGTAGAGATGGTGTGTCAGTATAT A T SMIM8 Ensembl:ENSG00000111850 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs569963829 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_348694 49862 RMVar_ID_49862 Human_SNP_ID_286057871 A-to-I Human chr6 + 87337875 87337875 87337875 GTTTTGAACTCCTGGCCTTAAGCGATTCTCCCACCTCAGCCTCCCAAATTGTTGTGATTACAGGC GTTTTGAACTCCTGGCCTTAAGCGATTCTCCCGCCTCAGCCTCCCAAATTGTTGTGATTACAGGC A G SMIM8 Ensembl:ENSG00000111850 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1308191648 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_348694 49863 RMVar_ID_49863 Human_SNP_ID_286093798 A-to-I Human chr6 + 87495915 87495915 87495915 CTGACCTTGTGATCCGCCCACCTCAACCTCCCAGAGTGCTGGGATTAGAGGCGTGAGCCACCGTG CTGACCTTGTGATCCGCCCACCTCAACCTCCCGGAGTGCTGGGATTAGAGGCGTGAGCCACCGTG A G AL049697.1,SLC35A1 Ensembl:ENSG00000213204,Ensembl:ENSG00000164414 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs561632738 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_347825,RMVar_hsa_circ_27274,RMVar_hsa_circ_240118 49864 RMVar_ID_49864 Human_SNP_ID_286095667 A-to-I Human chr6 - 87503693 87503693 87503693 TTATTATTATTATTGAAACAGAGTCTCGCACTATCACTCGAGCTGGTGTGCAGTGGCGCGATCTC TTATTATTATTATTGAAACAGAGTCTCGCACTGTCACTCGAGCTGGTGTGCAGTGGCGCGATCTC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs954609129 Functional Loss SNV dbSNP153 33..33 33 - - - 49865 RMVar_ID_49865 Human_SNP_ID_286097315 A-to-I Human chr6 - 87510703 87510703 87510703 TGCCCAGCCAATTTTGTATTTTTAGTAGAGACAGGATTTCTCCACGTTGGTCAGGCTGGTCCCCA TGCCCAGCCAATTTTGTATTTTTAGTAGAGACGGGATTTCTCCACGTTGGTCAGGCTGGTCCCCA T C - - Other Unknown GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs987392704 Functional Loss SNV dbSNP153 33..33 33 - - - 49866 RMVar_ID_49866 Human_SNP_ID_286101715 A-to-I Human chr6 - 87525726 87525726 87525726 CCTGGCCAACATAGTGAAAACCTGTCTCTACTAAAAACACAAAAATTAACTGGACGTGGTGGCGC CCTGGCCAACATAGTGAAAACCTGTCTCTACTGAAAACACAAAAATTAACTGGACGTGGTGGCGC T C RARS2 Ensembl:ENSG00000146282 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1279541016 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27662,RMVar_hsa_circ_103581,RMVar_hsa_circ_8419,RMVar_hsa_circ_369711,RMVar_hsa_circ_240123,RMVar_hsa_circ_240122,RMVar_hsa_circ_2279,RMVar_hsa_circ_13193,RMVar_hsa_circ_77958,RMVar_hsa_circ_40258,RMVar_hsa_circ_240124,RMVar_hsa_circ_6535,RMVar_hsa_circ_13455,RMVar_hsa_circ_283371,RMVar_hsa_circ_348662,RMVar_hsa_circ_44831,RMVar_hsa_circ_240125,RMVar_hsa_circ_240126 49867 RMVar_ID_49867 Human_SNP_ID_286101875 A-to-I Human chr6 - 87526333 87526333 87526333 TTTGTATTTCTTAGTAGAGATGGAGTTTCACCATGTTGCCCAGGCTGGTCTTGAACTCTTGGCTT TTTGTATTTCTTAGTAGAGATGGAGTTTCACCGTGTTGCCCAGGCTGGTCTTGAACTCTTGGCTT T C RARS2 Ensembl:ENSG00000146282 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1269711365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26030458 RMVar_hsa_circ_27662,RMVar_hsa_circ_103581,RMVar_hsa_circ_8419,RMVar_hsa_circ_369711,RMVar_hsa_circ_240123,RMVar_hsa_circ_240122,RMVar_hsa_circ_2279,RMVar_hsa_circ_13193,RMVar_hsa_circ_77958,RMVar_hsa_circ_40258,RMVar_hsa_circ_240124,RMVar_hsa_circ_6535,RMVar_hsa_circ_13455,RMVar_hsa_circ_283371,RMVar_hsa_circ_348662,RMVar_hsa_circ_44831,RMVar_hsa_circ_240125,RMVar_hsa_circ_240126 49868 RMVar_ID_49868 Human_SNP_ID_286101877 A-to-I Human chr6 - 87526336 87526336 87526336 ATTTTTGTATTTCTTAGTAGAGATGGAGTTTCACCATGTTGCCCAGGCTGGTCTTGAACTCTTGG ATTTTTGTATTTCTTAGTAGAGATGGAGTTTCGCCATGTTGCCCAGGCTGGTCTTGAACTCTTGG T C RARS2 Ensembl:ENSG00000146282 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs903837840 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27662,RMVar_hsa_circ_103581,RMVar_hsa_circ_8419,RMVar_hsa_circ_369711,RMVar_hsa_circ_240123,RMVar_hsa_circ_240122,RMVar_hsa_circ_2279,RMVar_hsa_circ_13193,RMVar_hsa_circ_77958,RMVar_hsa_circ_40258,RMVar_hsa_circ_240124,RMVar_hsa_circ_6535,RMVar_hsa_circ_13455,RMVar_hsa_circ_283371,RMVar_hsa_circ_348662,RMVar_hsa_circ_44831,RMVar_hsa_circ_240125,RMVar_hsa_circ_240126 49869 RMVar_ID_49869 Human_SNP_ID_286101895 A-to-I Human chr6 - 87526456 87526456 87526456 GCTGTAGTGCATTGGTGCTTTCTTGGCTCACTACAACCTCCACCTCCAGGTTCAACCTATTCTCC GCTGTAGTGCATTGGTGCTTTCTTGGCTCACTGCAACCTCCACCTCCAGGTTCAACCTATTCTCC T C RARS2 Ensembl:ENSG00000146282 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1197819696 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27662,RMVar_hsa_circ_103581,RMVar_hsa_circ_8419,RMVar_hsa_circ_369711,RMVar_hsa_circ_240123,RMVar_hsa_circ_240122,RMVar_hsa_circ_2279,RMVar_hsa_circ_13193,RMVar_hsa_circ_77958,RMVar_hsa_circ_40258,RMVar_hsa_circ_240124,RMVar_hsa_circ_6535,RMVar_hsa_circ_13455,RMVar_hsa_circ_283371,RMVar_hsa_circ_348662,RMVar_hsa_circ_44831,RMVar_hsa_circ_240125,RMVar_hsa_circ_240126 49870 RMVar_ID_49870 Human_SNP_ID_286102093 A-to-I Human chr6 - 87527221 87527221 87527221 CAGTGCAACCACTGCCTCCCAGGTTCAAGCGAATCTCCTGCCTCAGCCTCCCAAGTAGCTGGGAT CAGTGCAACCACTGCCTCCCAGGTTCAAGCGAGTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGAT T C RARS2 Ensembl:ENSG00000146282 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1167905604 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27662,RMVar_hsa_circ_103581,RMVar_hsa_circ_8419,RMVar_hsa_circ_369711,RMVar_hsa_circ_240123,RMVar_hsa_circ_240122,RMVar_hsa_circ_2279,RMVar_hsa_circ_13193,RMVar_hsa_circ_77958,RMVar_hsa_circ_40258,RMVar_hsa_circ_240124,RMVar_hsa_circ_6535,RMVar_hsa_circ_13455,RMVar_hsa_circ_283371,RMVar_hsa_circ_348662,RMVar_hsa_circ_44831,RMVar_hsa_circ_240125,RMVar_hsa_circ_240126 49871 RMVar_ID_49871 Human_SNP_ID_286102098 A-to-I Human chr6 - 87527233 87527233 87527233 ATGATCTTGGCTCAGTGCAACCACTGCCTCCCAGGTTCAAGCGAATCTCCTGCCTCAGCCTCCCA ATGATCTTGGCTCAGTGCAACCACTGCCTCCCGGGTTCAAGCGAATCTCCTGCCTCAGCCTCCCA T C RARS2 Ensembl:ENSG00000146282 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1443653057 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27662,RMVar_hsa_circ_103581,RMVar_hsa_circ_8419,RMVar_hsa_circ_369711,RMVar_hsa_circ_240123,RMVar_hsa_circ_240122,RMVar_hsa_circ_2279,RMVar_hsa_circ_13193,RMVar_hsa_circ_77958,RMVar_hsa_circ_40258,RMVar_hsa_circ_240124,RMVar_hsa_circ_6535,RMVar_hsa_circ_13455,RMVar_hsa_circ_283371,RMVar_hsa_circ_348662,RMVar_hsa_circ_44831,RMVar_hsa_circ_240125,RMVar_hsa_circ_240126 49872 RMVar_ID_49872 Human_SNP_ID_286108911 A-to-I Human chr6 - 87554535 87554535 87554535 GAAAGATGGCTTGAGCCTAGGAATTCAAGGTTACAGTGAGCTGTGATTGTCATGCACTCTAGCTC GAAAGATGGCTTGAGCCTAGGAATTCAAGGTTGCAGTGAGCTGTGATTGTCATGCACTCTAGCTC T C RARS2 Ensembl:ENSG00000146282 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1174580019 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40258,RMVar_hsa_circ_52774,RMVar_hsa_circ_53251,RMVar_hsa_circ_351026,RMVar_hsa_circ_93893,RMVar_hsa_circ_240129,RMVar_hsa_circ_276665,RMVar_hsa_circ_286834,RMVar_hsa_circ_344395,RMVar_hsa_circ_50700,RMVar_hsa_circ_14255,RMVar_hsa_circ_360509,RMVar_hsa_circ_240130,RMVar_hsa_circ_314950,RMVar_hsa_circ_30583,RMVar_hsa_circ_240131,RMVar_hsa_circ_13152 49873 RMVar_ID_49873 Human_SNP_ID_286108924 A-to-I Human chr6 - 87554621 87554621 87554621 AGACCTCGCCTCTTAAAAAAAATAGAAAAATTAGTTGTGCATGGTGGCACACTCCTGTAGTGACA AGACCTCGCCTCTTAAAAAAAATAGAAAAATTGGTTGTGCATGGTGGCACACTCCTGTAGTGACA T C RARS2 Ensembl:ENSG00000146282 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs992116493 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_40258,RMVar_hsa_circ_52774,RMVar_hsa_circ_53251,RMVar_hsa_circ_351026,RMVar_hsa_circ_93893,RMVar_hsa_circ_240129,RMVar_hsa_circ_276665,RMVar_hsa_circ_286834,RMVar_hsa_circ_344395,RMVar_hsa_circ_50700,RMVar_hsa_circ_14255,RMVar_hsa_circ_360509,RMVar_hsa_circ_240130,RMVar_hsa_circ_314950,RMVar_hsa_circ_30583,RMVar_hsa_circ_240131,RMVar_hsa_circ_13152 49874 RMVar_ID_49874 Human_SNP_ID_286108939 A-to-I Human chr6 - 87554680 87554680 87554680 GGAAGGCAAGGTGGGAGGATCACTTGAGGCCAAGAGTTCGAGACCAGCCTGGGCAACGCAGACCT GGAAGGCAAGGTGGGAGGATCACTTGAGGCCACGAGTTCGAGACCAGCCTGGGCAACGCAGACCT T G RARS2 Ensembl:ENSG00000146282 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1056971229 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17576143 RMVar_hsa_circ_40258,RMVar_hsa_circ_52774,RMVar_hsa_circ_53251,RMVar_hsa_circ_351026,RMVar_hsa_circ_93893,RMVar_hsa_circ_240129,RMVar_hsa_circ_276665,RMVar_hsa_circ_286834,RMVar_hsa_circ_344395,RMVar_hsa_circ_50700,RMVar_hsa_circ_14255,RMVar_hsa_circ_360509,RMVar_hsa_circ_240130,RMVar_hsa_circ_314950,RMVar_hsa_circ_30583,RMVar_hsa_circ_240131,RMVar_hsa_circ_13152 49875 RMVar_ID_49875 Human_SNP_ID_286112430 A-to-I Human chr6 - 87568241 87568241 87568241 CCCTTGCCTTGGTCTCCCAAAGTACTGGGATTACAAGTATGAACCACCACACCCAGCCTGTTTGT CCCTTGCCTTGGTCTCCCAAAGTACTGGGATTGCAAGTATGAACCACCACACCCAGCCTGTTTGT T C RARS2 Ensembl:ENSG00000146282 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1476379325 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_53251,RMVar_hsa_circ_351026,RMVar_hsa_circ_276665,RMVar_hsa_circ_14255,RMVar_hsa_circ_240130,RMVar_hsa_circ_30583,RMVar_hsa_circ_288251,RMVar_hsa_circ_360088,RMVar_hsa_circ_240134,RMVar_hsa_circ_33362,RMVar_hsa_circ_330064,RMVar_hsa_circ_240135 49876 RMVar_ID_49876 Human_SNP_ID_286112471 A-to-I Human chr6 - 87568378 87568378 87568378 CTCCCACCTCAGCCTCCAGAGTAGCTTGGACTACAGGCTCACGCCACTATGCCTGGCTGACATTT CTCCCACCTCAGCCTCCAGAGTAGCTTGGACTGCAGGCTCACGCCACTATGCCTGGCTGACATTT T C RARS2 Ensembl:ENSG00000146282 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1438431743 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_53251,RMVar_hsa_circ_351026,RMVar_hsa_circ_276665,RMVar_hsa_circ_14255,RMVar_hsa_circ_240130,RMVar_hsa_circ_30583,RMVar_hsa_circ_288251,RMVar_hsa_circ_360088,RMVar_hsa_circ_240134,RMVar_hsa_circ_33362,RMVar_hsa_circ_330064,RMVar_hsa_circ_240135 49877 RMVar_ID_49877 Human_SNP_ID_286128547 A-to-I Human chr6 + 87631693 87631693 87631693 TTTTGTATTTTTACTAGAGAGGGGGTTTTGCCAGGTTGGCTAGGCTGGTCTTGAACTCTGACCTC TTTTGTATTTTTACTAGAGAGGGGGTTTTGCCGGGTTGGCTAGGCTGGTCTTGAACTCTGACCTC A G ORC3 Ensembl:ENSG00000135336 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs533715945 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_240143,RMVar_hsa_circ_281231,RMVar_hsa_circ_240142,RMVar_hsa_circ_78024,RMVar_hsa_circ_276753,RMVar_hsa_circ_352732,RMVar_hsa_circ_332472,RMVar_hsa_circ_366149,RMVar_hsa_circ_50079,RMVar_hsa_circ_240151,RMVar_hsa_circ_240152 49878 RMVar_ID_49878 Human_SNP_ID_286132985 A-to-I Human chr6 + 87650750 87650750 87650750 GAGGACTAGACTGGGTGCAGTGGCTCACGCCTATAATCCCAGCACTTTGGGAAGCCGAGGTGGGC GAGGACTAGACTGGGTGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAAGCCGAGGTGGGC A G ORC3 Ensembl:ENSG00000135336 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs894484087 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_240143,RMVar_hsa_circ_78024,RMVar_hsa_circ_352732,RMVar_hsa_circ_50079 49879 RMVar_ID_49879 Human_SNP_ID_286133295 A-to-I Human chr6 + 87652072 87652071 87652072 AGGCGCCCACCACTACACCCGGCTAATTTTTTATAATTTTAGTAGAGACGAGGTTTCACCGTGGT AGGCGCCCACCACTACACCCGGCTAATTTTTT_TAATTTTAGTAGAGACGAGGTTTCACCGTGGT TA T ORC3 Ensembl:ENSG00000135336 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1344304274 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_240143,RMVar_hsa_circ_78024,RMVar_hsa_circ_352732,RMVar_hsa_circ_50079 49880 RMVar_ID_49880 Human_SNP_ID_286133296 A-to-I Human chr6 + 87652072 87652072 87652072 AGGCGCCCACCACTACACCCGGCTAATTTTTTATAATTTTAGTAGAGACGAGGTTTCACCGTGGT AGGCGCCCACCACTACACCCGGCTAATTTTTTGTAATTTTAGTAGAGACGAGGTTTCACCGTGGT A G ORC3 Ensembl:ENSG00000135336 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1271015696 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_240143,RMVar_hsa_circ_78024,RMVar_hsa_circ_352732,RMVar_hsa_circ_50079 49881 RMVar_ID_49881 Human_SNP_ID_286254382 A-to-I Human chr6 - 88160208 88160208 88160208 CGGCTCACTGCAGCCTCCGCTTCCTGGGTTCAAGCGATTCTCATGCTACCATGCCCGGCTAATTT CGGCTCACTGCAGCCTCCGCTTCCTGGGTTCAGGCGATTCTCATGCTACCATGCCCGGCTAATTT T C CNR1 Ensembl:ENSG00000118432 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs780955859 Functional Loss SNV dbSNP153 33..33 33 - - - 49882 RMVar_ID_49882 Human_SNP_ID_286254383 A-to-I Human chr6 - 88160208 88160208 88160208 CGGCTCACTGCAGCCTCCGCTTCCTGGGTTCAAGCGATTCTCATGCTACCATGCCCGGCTAATTT CGGCTCACTGCAGCCTCCGCTTCCTGGGTTCACGCGATTCTCATGCTACCATGCCCGGCTAATTT T G CNR1 Ensembl:ENSG00000118432 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs780955859 Functional Loss SNV dbSNP153 33..33 33 - - - 49883 RMVar_ID_49883 Human_SNP_ID_286498008 A-to-I Human chr6 + 89147657 89147657 89147657 GAGTTAAGGGTCAAGAATGAAGAGCGGTGGGCAGATCAGTTGAGGTCTGGAGTTCGAGACCCGCC GAGTTAAGGGTCAAGAATGAAGAGCGGTGGGCGGATCAGTTGAGGTCTGGAGTTCGAGACCCGCC A G PM20D2 Ensembl:ENSG00000146281 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs370256822 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_240192 49884 RMVar_ID_49884 Human_SNP_ID_286498155 A-to-I Human chr6 + 89148055 89148055 89148055 CCAGGCCGAGTGCAGTGGTCCTATCTCGGCTCACTACAACCTCCGCCTCCCGGGTTCAGGCGATC CCAGGCCGAGTGCAGTGGTCCTATCTCGGCTCGCTACAACCTCCGCCTCCCGGGTTCAGGCGATC A G PM20D2 Ensembl:ENSG00000146281 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1364746020 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_240192 49885 RMVar_ID_49885 Human_SNP_ID_286498156 A-to-I Human chr6 + 89148058 89148058 89148058 GGCCGAGTGCAGTGGTCCTATCTCGGCTCACTACAACCTCCGCCTCCCGGGTTCAGGCGATCCTC GGCCGAGTGCAGTGGTCCTATCTCGGCTCACTGCAACCTCCGCCTCCCGGGTTCAGGCGATCCTC A G PM20D2 Ensembl:ENSG00000146281 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1487262252 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_240192 49886 RMVar_ID_49886 Human_SNP_ID_286498181 A-to-I Human chr6 + 89148159 89148159 89148159 GCCACCACGCCCAGCTAATTTTTGCATTTTTTAGTAGAGACAGGATTTCGCCATGTTGGCCTGGC GCCACCACGCCCAGCTAATTTTTGCATTTTTTGGTAGAGACAGGATTTCGCCATGTTGGCCTGGC A G PM20D2 Ensembl:ENSG00000146281 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1299000819 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_240192 49887 RMVar_ID_49887 Human_SNP_ID_286544922 A-to-I Human chr6 - 89341502 89341408 89341502 GAACTACTGGCCTCAGGCAGTCCTCCCATCTCAGCCTCCCAAAGTGCTAGGATGACAGGTGTCAC GAACTACTGGCCTCAGGCAGTCCTCCCATCT__________________________________ GAAGAAAAGCTTAACAATTAAAGAGGAATTAGATCAATAGTTTTCCTTGGCCAGGTATGATGGTGACACCTGTCATCCTAGCACTTTGGGAGGCT G UBE2J1 Ensembl:ENSG00000198833 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1562419949 Functional Loss DEL dbSNP153 33..65 33 - - - RMVar_hsa_circ_240210,RMVar_hsa_circ_79484,RMVar_hsa_circ_122891,RMVar_hsa_circ_98764,RMVar_hsa_circ_240206,RMVar_hsa_circ_240203,RMVar_hsa_circ_240204,RMVar_hsa_circ_240202,RMVar_hsa_circ_240205,RMVar_hsa_circ_319718,RMVar_hsa_circ_311863,RMVar_hsa_circ_240208,RMVar_hsa_circ_322488 49888 RMVar_ID_49888 Human_SNP_ID_286550563 A-to-I Human chr6 - 89366356 89366356 89366356 GGCTAATTCTTAAATTTTGTTTTTGTAGAGACAGGATCTCACTGTGTTGCCCAAGATGGTCTCAA GGCTAATTCTTAAATTTTGTTTTTGTAGAGACGGGATCTCACTGTGTTGCCCAAGATGGTCTCAA T C RRAGD Ensembl:ENSG00000025039 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1265016643 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2029665,Human_RBP_ID_7644626,Human_RBP_ID_18083279 RMVar_hsa_circ_240212,RMVar_hsa_circ_266882 49889 RMVar_ID_49889 Human_SNP_ID_286580182 A-to-I Human chr6 + 89496652 89496652 89496652 TTAAGCAATTCTCCTGCCTCAGCCTCCCGAATAGCTGGGATTACAGGCACCTGCCACCACACCCA TTAAGCAATTCTCCTGCCTCAGCCTCCCGAATGGCTGGGATTACAGGCACCTGCCACCACACCCA A G ANKRD6 Ensembl:ENSG00000135299 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1266264286 Functional Loss SNV dbSNP153 33..33 33 - - - 49890 RMVar_ID_49890 Human_SNP_ID_286612392 A-to-I Human chr6 - 89634456 89634456 89634456 AGCAATCCACCTGCCTCGGTGGCCAGAGTGCTAGGATTACAGGTGTGAGTTGTTTTTTTTTTTAA AGCAATCCACCTGCCTCGGTGGCCAGAGTGCTGGGATTACAGGTGTGAGTTGTTTTTTTTTTTAA T C LYRM2 Ensembl:ENSG00000083099 Protein coding intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1283226565 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7644988 49891 RMVar_ID_49891 Human_SNP_ID_286612408 A-to-I Human chr6 - 89634503 89634503 89634503 GGGGAATCTCACTTTGTTGCCAGGCTAGTCTCAAACTCCTGGGCTCAAGCAATCCACCTGCCTCG GGGGAATCTCACTTTGTTGCCAGGCTAGTCTCGAACTCCTGGGCTCAAGCAATCCACCTGCCTCG T C LYRM2 Ensembl:ENSG00000083099 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs13863 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_670235,Human_RBP_ID_26540261 49892 RMVar_ID_49892 Human_SNP_ID_286612447 A-to-I Human chr6 - 89634678 89634678 89634678 TTTTGAGACAGGGTCTCTGTTGCACAAGCTGGAGTGTGGTGGCGCGAACATGGCTCACTGCAACC TTTTGAGACAGGGTCTCTGTTGCACAAGCTGGGGTGTGGTGGCGCGAACATGGCTCACTGCAACC T C LYRM2 Ensembl:ENSG00000083099 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1445984783 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7644997 49893 RMVar_ID_49893 Human_SNP_ID_286612502 A-to-I Human chr6 - 89634850 89634848 89634850 GGGAGGCAGAGGCTGCAGTGAGCCGAGAACACACTACTGCACTACAGCCTGGGCGAAAGAGTGAG GGGAGGCAGAGGCTGCAGTGAGCCGAGAACAC__TACTGCACTACAGCCTGGGCGAAAGAGTGAG AGT A LYRM2 Ensembl:ENSG00000083099 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1366811335 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_10305185 49894 RMVar_ID_49894 Human_SNP_ID_286612536 A-to-I Human chr6 - 89634982 89634982 89634982 ACTTTGGGAGGCTGAGGTGGGTGGATCACTTTAGGTCAGGATTTCGAGACTAGCTAGGCCACTAG ACTTTGGGAGGCTGAGGTGGGTGGATCACTTTCGGTCAGGATTTCGAGACTAGCTAGGCCACTAG T G LYRM2 Ensembl:ENSG00000083099 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1422782756 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7645004,Human_RBP_ID_15908083,Human_RBP_ID_26032638 49895 RMVar_ID_49895 Human_SNP_ID_286612983 A-to-I Human chr6 - 89636900 89636900 89636900 GTGGTAGGTGGATCACTTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAGCATGGTGAAACCTCAT GTGGTAGGTGGATCACTTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAGCATGGTGAAACCTCAT T C LYRM2 Ensembl:ENSG00000083099 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1371233425 Functional Loss SNV dbSNP153 33..33 33 - - - 49896 RMVar_ID_49896 Human_SNP_ID_286635216 A-to-I Human chr6 - 89723980 89723980 89723980 TGCCACTATGCCCAGCTAATTTTTGTATTTTTAGTGAAGACAGGGTTTCGTCATGCTGGTCAGGA TGCCACTATGCCCAGCTAATTTTTGTATTTTTGGTGAAGACAGGGTTTCGTCATGCTGGTCAGGA T C MDN1 Ensembl:ENSG00000112159 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1265479295 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124963,RMVar_hsa_circ_240235,RMVar_hsa_circ_269533,RMVar_hsa_circ_95989,RMVar_hsa_circ_125853,RMVar_hsa_circ_240243,RMVar_hsa_circ_240245,RMVar_hsa_circ_240244,RMVar_hsa_circ_107596,RMVar_hsa_circ_61890,RMVar_hsa_circ_128122,RMVar_hsa_circ_240250,RMVar_hsa_circ_125444,RMVar_hsa_circ_240254,RMVar_hsa_circ_122539,RMVar_hsa_circ_240252,RMVar_hsa_circ_77464,RMVar_hsa_circ_240253,RMVar_hsa_circ_265022,RMVar_hsa_circ_269189,RMVar_hsa_circ_240260,RMVar_hsa_circ_116956,RMVar_hsa_circ_357670,RMVar_hsa_circ_117784,RMVar_hsa_circ_96630,RMVar_hsa_circ_114984,RMVar_hsa_circ_240262,RMVar_hsa_circ_93682,RMVar_hsa_circ_240263,RMVar_hsa_circ_240261,RMVar_hsa_circ_76756,RMVar_hsa_circ_240259,RMVar_hsa_circ_76109,RMVar_hsa_circ_240265,RMVar_hsa_circ_240266,RMVar_hsa_circ_25965,RMVar_hsa_circ_58449,RMVar_hsa_circ_63777,RMVar_hsa_circ_87333,RMVar_hsa_circ_123487,RMVar_hsa_circ_51774,RMVar_hsa_circ_73013,RMVar_hsa_circ_79291,RMVar_hsa_circ_240269,RMVar_hsa_circ_25824,RMVar_hsa_circ_240268,RMVar_hsa_circ_108649,RMVar_hsa_circ_240272,RMVar_hsa_circ_240273,RMVar_hsa_circ_100109,RMVar_hsa_circ_269119,RMVar_hsa_circ_76398,RMVar_hsa_circ_240275,RMVar_hsa_circ_346311,RMVar_hsa_circ_116655,RMVar_hsa_circ_125139,RMVar_hsa_circ_240276,RMVar_hsa_circ_240277,RMVar_hsa_circ_240281,RMVar_hsa_circ_240280,RMVar_hsa_circ_240282,RMVar_hsa_circ_103726,RMVar_hsa_circ_266447,RMVar_hsa_circ_286620,RMVar_hsa_circ_65304,RMVar_hsa_circ_240283,RMVar_hsa_circ_120459,RMVar_hsa_circ_355211,RMVar_hsa_circ_368760,RMVar_hsa_circ_291088,RMVar_hsa_circ_111135,RMVar_hsa_circ_118841,RMVar_hsa_circ_99087,RMVar_hsa_circ_240286,RMVar_hsa_circ_240287,RMVar_hsa_circ_240288,RMVar_hsa_circ_240285 49897 RMVar_ID_49897 Human_SNP_ID_286635648 A-to-I Human chr6 - 89725772 89725772 89725772 GGGAGTTTGAGACCATCCTGGACAACATAACAAGACCTTGGCTCTACCAAAAAAAAAAAAAAAAG GGGAGTTTGAGACCATCCTGGACAACATAACACGACCTTGGCTCTACCAAAAAAAAAAAAAAAAG T G MDN1 Ensembl:ENSG00000112159 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973433457 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95989,RMVar_hsa_circ_125853,RMVar_hsa_circ_240243,RMVar_hsa_circ_240245,RMVar_hsa_circ_240244,RMVar_hsa_circ_107596,RMVar_hsa_circ_240254,RMVar_hsa_circ_77464,RMVar_hsa_circ_265022,RMVar_hsa_circ_269189,RMVar_hsa_circ_240260,RMVar_hsa_circ_116956,RMVar_hsa_circ_117784,RMVar_hsa_circ_96630,RMVar_hsa_circ_114984,RMVar_hsa_circ_240262,RMVar_hsa_circ_93682,RMVar_hsa_circ_240263,RMVar_hsa_circ_240261,RMVar_hsa_circ_76756,RMVar_hsa_circ_240259,RMVar_hsa_circ_76109,RMVar_hsa_circ_240265,RMVar_hsa_circ_240266,RMVar_hsa_circ_25965,RMVar_hsa_circ_58449,RMVar_hsa_circ_87333,RMVar_hsa_circ_123487,RMVar_hsa_circ_51774,RMVar_hsa_circ_73013,RMVar_hsa_circ_79291,RMVar_hsa_circ_240269,RMVar_hsa_circ_25824,RMVar_hsa_circ_240268,RMVar_hsa_circ_108649,RMVar_hsa_circ_240272,RMVar_hsa_circ_240273,RMVar_hsa_circ_100109,RMVar_hsa_circ_269119,RMVar_hsa_circ_76398,RMVar_hsa_circ_240275,RMVar_hsa_circ_116655,RMVar_hsa_circ_125139,RMVar_hsa_circ_240277,RMVar_hsa_circ_240281,RMVar_hsa_circ_240280,RMVar_hsa_circ_240282,RMVar_hsa_circ_103726,RMVar_hsa_circ_266447,RMVar_hsa_circ_42388,RMVar_hsa_circ_65304,RMVar_hsa_circ_240283,RMVar_hsa_circ_120459,RMVar_hsa_circ_355211,RMVar_hsa_circ_368760,RMVar_hsa_circ_111135,RMVar_hsa_circ_118841,RMVar_hsa_circ_99087,RMVar_hsa_circ_240286,RMVar_hsa_circ_240287,RMVar_hsa_circ_240288,RMVar_hsa_circ_55432,RMVar_hsa_circ_353298,RMVar_hsa_circ_34051 49898 RMVar_ID_49898 Human_SNP_ID_286647463 A-to-I Human chr6 - 89770798 89770798 89770798 GTACAGTTGATCTAAAGTGTAAGTTCTGGGCCAGGCGTGGCGGCTCACACCTGTAATCCCAGCAC GTACAGTTGATCTAAAGTGTAAGTTCTGGGCCGGGCGTGGCGGCTCACACCTGTAATCCCAGCAC T C MDN1 Ensembl:ENSG00000112159 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs892304432 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17632717 RMVar_hsa_circ_114984,RMVar_hsa_circ_240263,RMVar_hsa_circ_76756,RMVar_hsa_circ_240266,RMVar_hsa_circ_87333,RMVar_hsa_circ_240268,RMVar_hsa_circ_100109,RMVar_hsa_circ_240275,RMVar_hsa_circ_116655,RMVar_hsa_circ_240281,RMVar_hsa_circ_240283,RMVar_hsa_circ_120459,RMVar_hsa_circ_99087,RMVar_hsa_circ_240288,RMVar_hsa_circ_60076,RMVar_hsa_circ_43692,RMVar_hsa_circ_99826,RMVar_hsa_circ_107678,RMVar_hsa_circ_240291,RMVar_hsa_circ_43047,RMVar_hsa_circ_70086,RMVar_hsa_circ_240294,RMVar_hsa_circ_240293,RMVar_hsa_circ_101808,RMVar_hsa_circ_267543,RMVar_hsa_circ_111116,RMVar_hsa_circ_57841,RMVar_hsa_circ_240297,RMVar_hsa_circ_374210,RMVar_hsa_circ_121802,RMVar_hsa_circ_79514,RMVar_hsa_circ_240300,RMVar_hsa_circ_240301,RMVar_hsa_circ_240302,RMVar_hsa_circ_240303,RMVar_hsa_circ_340022,RMVar_hsa_circ_376173,RMVar_hsa_circ_50451,RMVar_hsa_circ_240307,RMVar_hsa_circ_83823,RMVar_hsa_circ_94525,RMVar_hsa_circ_240305,RMVar_hsa_circ_89930,RMVar_hsa_circ_240308,RMVar_hsa_circ_240306 49899 RMVar_ID_49899 Human_SNP_ID_286656824 A-to-I Human chr6 - 89804977 89804977 89804977 GCTAGAGTGCAGTGGCACGATCTCGGCTCACTACAGGCTCCGCCTCCCGGGGTTCACACCATTCT GCTAGAGTGCAGTGGCACGATCTCGGCTCACTGCAGGCTCCGCCTCCCGGGGTTCACACCATTCT T C MDN1 Ensembl:ENSG00000112159 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs533586043 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15910604 RMVar_hsa_circ_240319,RMVar_hsa_circ_86713 49900 RMVar_ID_49900 Human_SNP_ID_286658603 A-to-I Human chr6 - 89811610 89811610 89811610 GAAACCCCATCTCTACTAAAAATACAAAAATTAGCTGGGCGTGGTGGCACACTCCTGTAGTCCCA GAAACCCCATCTCTACTAAAAATACAAAAATTTGCTGGGCGTGGTGGCACACTCCTGTAGTCCCA T A MDN1 Ensembl:ENSG00000112159 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs754493210 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_240319,RMVar_hsa_circ_86713 49901 RMVar_ID_49901 Human_SNP_ID_286664664 A-to-I Human chr6 + 89834226 89834226 89834226 CATAAGGTCAGGAGTTCAAGACCAGCCTGGCCAAGATGGTGAAACCCTGTCTCTACTAAAAATAC CATAAGGTCAGGAGTTCAAGACCAGCCTGGCCCAGATGGTGAAACCCTGTCTCTACTAAAAATAC A C CASP8AP2 Ensembl:ENSG00000118412 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1330690507 Functional Loss SNV dbSNP153 33..33 33 - - - 49902 RMVar_ID_49902 Human_SNP_ID_286664681 A-to-I Human chr6 + 89834280 89834280 89834280 ACTAAAAATACAAAAAATTAGCTGGGCGCGGCAGCAGGCCCCTGTAATCCCAGCTACTGAGGAGG ACTAAAAATACAAAAAATTAGCTGGGCGCGGCTGCAGGCCCCTGTAATCCCAGCTACTGAGGAGG A T CASP8AP2 Ensembl:ENSG00000118412 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1401466918 Functional Loss SNV dbSNP153 33..33 33 - - - 49903 RMVar_ID_49903 Human_SNP_ID_286665365 A-to-I Human chr6 + 89836881 89836881 89836881 CCCACCTCAGCCTCCTAAGTATGGTTGGGACTATAGGAGTGTGTCACCACGCCTGGCTAATTTTT CCCACCTCAGCCTCCTAAGTATGGTTGGGACTTTAGGAGTGTGTCACCACGCCTGGCTAATTTTT A T CASP8AP2 Ensembl:ENSG00000118412 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs547732143 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7645693,Human_RBP_ID_15911262,Human_RBP_ID_24176543 49904 RMVar_ID_49904 Human_SNP_ID_286665991 A-to-I Human chr6 + 89839400 89839400 89839400 AATCTCTATTGTAACAATTTTTTTTTTTTTTGAGACAGAATCGCTGTGTTGCCCAAGCTGGAGTG AATCTCTATTGTAACAATTTTTTTTTTTTTTGTGACAGAATCGCTGTGTTGCCCAAGCTGGAGTG A T CASP8AP2 Ensembl:ENSG00000118412 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1251627583 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7645736 49905 RMVar_ID_49905 Human_SNP_ID_286666114 A-to-I Human chr6 + 89839864 89839864 89839864 ATCACCTGAGGTCAGAAGTTTAAGATCAGCCTAGCCAACATGGTGAAACCCCGTCTCTACTAAAA ATCACCTGAGGTCAGAAGTTTAAGATCAGCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAA A G CASP8AP2 Ensembl:ENSG00000118412 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1360464025 Functional Loss SNV dbSNP153 33..33 33 - - - 49906 RMVar_ID_49906 Human_SNP_ID_286667777 A-to-I Human chr6 + 89845733 89845733 89845733 GTTTATTTGTTTTGTTTTTGAGACAGGGTCTCACTCTGTCACCCAGGCTGCAGTGCAGTGGCACT GTTTATTTGTTTTGTTTTTGAGACAGGGTCTCTCTCTGTCACCCAGGCTGCAGTGCAGTGGCACT A T CASP8AP2 Ensembl:ENSG00000118412 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947570791 Functional Loss SNV dbSNP153 33..33 33 - - - 49907 RMVar_ID_49907 Human_SNP_ID_286667804 A-to-I Human chr6 + 89845795 89845795 89845795 ACTATCGTGGCTTACTGCAACCTCTCCCTGCCAGGCTCAAGCGATCCTCCTGCTTCAGCCACCAA ACTATCGTGGCTTACTGCAACCTCTCCCTGCCGGGCTCAAGCGATCCTCCTGCTTCAGCCACCAA A G CASP8AP2 Ensembl:ENSG00000118412 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs369921075 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8651518 49908 RMVar_ID_49908 Human_SNP_ID_286667874 A-to-I Human chr6 + 89846129 89846129 89846129 GTTAGAGAGAAAGGCCAGGCATGGGGGCTTACACCTGTAATTCCAGCACTTTGAGAGGCTGAGGT GTTAGAGAGAAAGGCCAGGCATGGGGGCTTACGCCTGTAATTCCAGCACTTTGAGAGGCTGAGGT A G CASP8AP2 Ensembl:ENSG00000118412 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1369393780 Functional Loss SNV dbSNP153 33..33 33 - - - 49909 RMVar_ID_49909 Human_SNP_ID_286667882 A-to-I Human chr6 + 89846189 89846189 89846189 GAGGTGGGTGGATTGCTTAAGGCCAGGAGTTCAAGACCAGCCTGGCCAACGTGGCAGACAGGCAA GAGGTGGGTGGATTGCTTAAGGCCAGGAGTTCCAGACCAGCCTGGCCAACGTGGCAGACAGGCAA A C CASP8AP2 Ensembl:ENSG00000118412 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1402013908 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23196046 49910 RMVar_ID_49910 Human_SNP_ID_286670002 A-to-I Human chr6 + 89854225 89854225 89854225 GGTAGCTCACGCCTGTAATCCCAGCACTTTGCAAGGCCGAGGCGGGCGGATCCCCTGAGGTCAGG GGTAGCTCACGCCTGTAATCCCAGCACTTTGCGAGGCCGAGGCGGGCGGATCCCCTGAGGTCAGG A G CASP8AP2 Ensembl:ENSG00000118412 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1297635890 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98471,RMVar_hsa_circ_279621,RMVar_hsa_circ_311216,RMVar_hsa_circ_366469,RMVar_hsa_circ_275762,RMVar_hsa_circ_240326,RMVar_hsa_circ_240327,RMVar_hsa_circ_240328,RMVar_hsa_circ_240325,RMVar_hsa_circ_240329,RMVar_hsa_circ_281960,RMVar_hsa_circ_295073,RMVar_hsa_circ_306546,RMVar_hsa_circ_240330 49911 RMVar_ID_49911 Human_SNP_ID_286670020 A-to-I Human chr6 + 89854283 89854283 89854283 GGTCAGGAGTTGGAGACCAGCCTGGCCAACATAGTGAAAACTCGTCTCTACTACAAATACAAAAA GGTCAGGAGTTGGAGACCAGCCTGGCCAACATGGTGAAAACTCGTCTCTACTACAAATACAAAAA A G CASP8AP2 Ensembl:ENSG00000118412 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1225496874 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98471,RMVar_hsa_circ_279621,RMVar_hsa_circ_311216,RMVar_hsa_circ_366469,RMVar_hsa_circ_275762,RMVar_hsa_circ_240326,RMVar_hsa_circ_240327,RMVar_hsa_circ_240328,RMVar_hsa_circ_240325,RMVar_hsa_circ_240329,RMVar_hsa_circ_281960,RMVar_hsa_circ_295073,RMVar_hsa_circ_306546,RMVar_hsa_circ_240330 49912 RMVar_ID_49912 Human_SNP_ID_286670121 A-to-I Human chr6 + 89854583 89854583 89854583 CCAACATGGTGAAACACCATCTCACCATCTCTACTAAAAATACAAAAATTAGTGGGGCGTGGTGG CCAACATGGTGAAACACCATCTCACCATCTCTGCTAAAAATACAAAAATTAGTGGGGCGTGGTGG A G CASP8AP2 Ensembl:ENSG00000118412 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs962427589 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_98471,RMVar_hsa_circ_279621,RMVar_hsa_circ_311216,RMVar_hsa_circ_366469,RMVar_hsa_circ_275762,RMVar_hsa_circ_240326,RMVar_hsa_circ_240327,RMVar_hsa_circ_240328,RMVar_hsa_circ_240325,RMVar_hsa_circ_240329,RMVar_hsa_circ_281960,RMVar_hsa_circ_295073,RMVar_hsa_circ_306546,RMVar_hsa_circ_240330 49913 RMVar_ID_49913 Human_SNP_ID_286670822 A-to-I Human chr6 + 89857474 89857474 89857474 GAGATAACAGGTGCACAACACCATGTCTGCCTAATTTTTTTATTTTTTATTTTTGGTGGAGACAG GAGATAACAGGTGCACAACACCATGTCTGCCTGATTTTTTTATTTTTTATTTTTGGTGGAGACAG A G CASP8AP2 Ensembl:ENSG00000118412 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886513549 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7645837 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_361051 49914 RMVar_ID_49914 Human_SNP_ID_286670823 A-to-I Human chr6 + 89857474 89857474 89857474 GAGATAACAGGTGCACAACACCATGTCTGCCTAATTTTTTTATTTTTTATTTTTGGTGGAGACAG GAGATAACAGGTGCACAACACCATGTCTGCCTTATTTTTTTATTTTTTATTTTTGGTGGAGACAG A T CASP8AP2 Ensembl:ENSG00000118412 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886513549 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7645837 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_361051 49915 RMVar_ID_49915 Human_SNP_ID_286671419 A-to-I Human chr6 + 89859674 89859674 89859674 GGTTCAAGCGATCCTCCCACCTCAGTCTCCCGAGTAGCTGGGATTACAGGCATGCACCACCTGTA GGTTCAAGCGATCCTCCCACCTCAGTCTCCCGGGTAGCTGGGATTACAGGCATGCACCACCTGTA A G CASP8AP2 Ensembl:ENSG00000118412 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs971871207 Functional Loss SNV dbSNP153 33..33 33 - - - 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_361051 49916 RMVar_ID_49916 Human_SNP_ID_621549175 A-to-I Human chr17 + 30069054 30069053 30069054 ACTGCTGTTCTGGATTTCATTGAAGATTACTTAAAAAAAGTGTGTAAACTTTACTCAGAACAAAG ACTGCTGTTCTGGATTTCATTGAAGATTACTT_AAAAAAGTGTGTAAACTTTACTCAGAACAAAG TA T AC104996.2,EFCAB5 Ensembl:ENSG00000266876,Ensembl:ENSG00000176927 Pseudogene,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs537851106 Functional Loss DEL dbSNP153 33..33 33 - - - 49917 RMVar_ID_49917 Human_SNP_ID_621549177 A-to-I Human chr17 + 30069054 30069054 30069054 ACTGCTGTTCTGGATTTCATTGAAGATTACTTAAAAAAAGTGTGTAAACTTTACTCAGAACAAAG ACTGCTGTTCTGGATTTCATTGAAGATTACTTTAAAAAAGTGTGTAAACTTTACTCAGAACAAAG A T AC104996.2,EFCAB5 Ensembl:ENSG00000266876,Ensembl:ENSG00000176927 Pseudogene,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs554582315 Functional Loss SNV dbSNP153 33..33 33 - - - 49918 RMVar_ID_49918 Human_SNP_ID_621549186 A-to-I Human chr17 + 30069100 30069099 30069101 AACTTTACTCAGAACAAAGAGCCATCCGAGTTAAAAGAGTGGTGGATAAGAAAAGAATATCTAAG AACTTTACTCAGAACAAAGAGCCATCCGAGTT__AAGAGTGGTGGATAAGAAAAGAATATCTAAG TAA T AC104996.2,EFCAB5 Ensembl:ENSG00000266876,Ensembl:ENSG00000176927 Pseudogene,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1047740744 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_17379691,Human_RBP_ID_18531136 49919 RMVar_ID_49919 Human_SNP_ID_621562081 A-to-I Human chr17 + 30123177 30123177 30123177 GCTGGAGTGCAGTGGCACGAACTTGGCTCACTACAACCTCCACCTCCTGGGTTCAACCAGTTTCC GCTGGAGTGCAGTGGCACGAACTTGGCTCACTGCAACCTCCACCTCCTGGGTTCAACCAGTTTCC A G NSRP1 Ensembl:ENSG00000126653 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs779091522 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61605,RMVar_hsa_circ_373114,RMVar_hsa_circ_183217 49920 RMVar_ID_49920 Human_SNP_ID_621562287 A-to-I Human chr17 + 30124065 30124065 30124065 CGGAGGCTGAGGTGGGAGAATCGCTTGAGGCTAGGAGTTCAAGTCCAGCCTGGGCAACAGCGAGA CGGAGGCTGAGGTGGGAGAATCGCTTGAGGCTCGGAGTTCAAGTCCAGCCTGGGCAACAGCGAGA A C NSRP1 Ensembl:ENSG00000126653 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1250087760 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1180991,Human_RBP_ID_6577232,Human_RBP_ID_8815781,Human_RBP_ID_9287105,Human_RBP_ID_9884470,Human_RBP_ID_12951383,Human_RBP_ID_22803825,Human_RBP_ID_25339494 RMVar_hsa_circ_61605,RMVar_hsa_circ_373114,RMVar_hsa_circ_183217 49921 RMVar_ID_49921 Human_SNP_ID_621563056 A-to-I Human chr17 + 30127688 30127688 30127688 CTTGTGCCTCAGCCTCCCAAAGTGTCGGGATTATAGGTGTGAACTACTGTAACTGGCCTAGTTGT CTTGTGCCTCAGCCTCCCAAAGTGTCGGGATTGTAGGTGTGAACTACTGTAACTGGCCTAGTTGT A G NSRP1 Ensembl:ENSG00000126653 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs970274837 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12951532 RMVar_hsa_circ_61605,RMVar_hsa_circ_373114,RMVar_hsa_circ_183217 49922 RMVar_ID_49922 Human_SNP_ID_621566031 A-to-I Human chr17 + 30139769 30139768 30139770 ATTTGAGGCCGGGCATGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGCGG ATTTGAGGCCGGGCATGGTGGCTCACGCCTGT__TCCCAGCACTTTGGGAGGCTGAGGCGGGCGG TAA T NSRP1 Ensembl:ENSG00000126653 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1446732274 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_61605,RMVar_hsa_circ_373114,RMVar_hsa_circ_183217 49923 RMVar_ID_49923 Human_SNP_ID_621566032 A-to-I Human chr17 + 30139769 30139769 30139769 ATTTGAGGCCGGGCATGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGCGG ATTTGAGGCCGGGCATGGTGGCTCACGCCTGTTATCCCAGCACTTTGGGAGGCTGAGGCGGGCGG A T NSRP1 Ensembl:ENSG00000126653 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs906068037 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61605,RMVar_hsa_circ_373114,RMVar_hsa_circ_183217 49924 RMVar_ID_49924 Human_SNP_ID_621566509 A-to-I Human chr17 + 30141747 30141747 30141747 AATATCGGCTGGGCGCAGTGGCTCATGCTGGTAATCCCAGCACTGTGGGAGGCCAAAGTGGGCGG AATATCGGCTGGGCGCAGTGGCTCATGCTGGTGATCCCAGCACTGTGGGAGGCCAAAGTGGGCGG A G NSRP1 Ensembl:ENSG00000126653 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1236082069 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61605,RMVar_hsa_circ_373114,RMVar_hsa_circ_183217 49925 RMVar_ID_49925 Human_SNP_ID_621566688 A-to-I Human chr17 + 30142541 30142541 30142541 AGTCGTAGAAATGAAGTCTTGCTATGTTGCCCAGGCTGGTTTGGAACTCCTGGCCTCAAACGATC AGTCGTAGAAATGAAGTCTTGCTATGTTGCCCGGGCTGGTTTGGAACTCCTGGCCTCAAACGATC A G NSRP1 Ensembl:ENSG00000126653 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1197411414 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12952116,Human_RBP_ID_26640994 RMVar_hsa_circ_61605,RMVar_hsa_circ_373114,RMVar_hsa_circ_183217 49926 RMVar_ID_49926 Human_SNP_ID_621567814 A-to-I Human chr17 + 30147268 30147268 30147268 ATGCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCCTCCGCCACCATGCCCCAGCTAATTTT ATGCTGCCTCAGCCTCCCAAGTAGCTGGGATTGCAGGCCTCCGCCACCATGCCCCAGCTAATTTT A G NSRP1 Ensembl:ENSG00000126653 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1257423536 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61605,RMVar_hsa_circ_373114,RMVar_hsa_circ_183217 49927 RMVar_ID_49927 Human_SNP_ID_621569776 A-to-I Human chr17 + 30154672 30154672 30154672 AAGTCAAGGCTCCTGTGAGCCATGATCGTGCCACTGAACTCCAGCCTGGGCAACAGAGTGAGACC AAGTCAAGGCTCCTGTGAGCCATGATCGTGCCGCTGAACTCCAGCCTGGGCAACAGAGTGAGACC A G NSRP1 Ensembl:ENSG00000126653 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs562011933 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25264751 RMVar_hsa_circ_61605,RMVar_hsa_circ_373114,RMVar_hsa_circ_183217 49928 RMVar_ID_49928 Human_SNP_ID_621578453 A-to-I Human chr17 + 30188875 30188875 30188875 CGGGGTTTTACTATGTTGTCTAGGCTGGTCTCAAACTCCTAGGCTCAAGCAATTTCGCCTGCCTC CGGGGTTTTACTATGTTGTCTAGGCTGGTCTCGAACTCCTAGGCTCAAGCAATTTCGCCTGCCTC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs926555327 Functional Loss SNV dbSNP153 33..33 33 - - - 49929 RMVar_ID_49929 Human_SNP_ID_621628679 A-to-I Human chr17 + 30400884 30400884 30400884 TATTTTTAGTGGAGATGGGGTTTCACCATGTTAGCCAAGATAGTCTTGATCTCCTGACCTCGTGA TATTTTTAGTGGAGATGGGGTTTCACCATGTTGGCCAAGATAGTCTTGATCTCCTGACCTCGTGA A G CPD Ensembl:ENSG00000108582 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1437847475 Functional Loss SNV dbSNP153 33..33 33 - - - 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 49930 RMVar_ID_49930 Human_SNP_ID_621646690 A-to-I Human chr17 + 30480160 30480160 30480160 GAAACCCCGTCTTTACTAAAAATACAAAAATTAGCCAGGCATGGTGGTGTGTGCCTGTAGTCCCA GAAACCCCGTCTTTACTAAAAATACAAAAATTGGCCAGGCATGGTGGTGTGTGCCTGTAGTCCCA A G GOSR1 Ensembl:ENSG00000108587 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs547480422 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1800513 49931 RMVar_ID_49931 Human_SNP_ID_621648060 A-to-I Human chr17 + 30485379 30485379 30485379 GCCTCAACCTCCCAAGCTCAAACAAGCCTCCTACCTCAGCGTCCTGAGCATCTGGGACCACAAGC GCCTCAACCTCCCAAGCTCAAACAAGCCTCCTGCCTCAGCGTCCTGAGCATCTGGGACCACAAGC A G GOSR1 Ensembl:ENSG00000108587 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1034611180 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183234,RMVar_hsa_circ_108830,RMVar_hsa_circ_341664,RMVar_hsa_circ_277054,RMVar_hsa_circ_272577,RMVar_hsa_circ_183236,RMVar_hsa_circ_34147,RMVar_hsa_circ_183235,RMVar_hsa_circ_20676,RMVar_hsa_circ_183239,RMVar_hsa_circ_57502,RMVar_hsa_circ_293685,RMVar_hsa_circ_308977,RMVar_hsa_circ_270274,RMVar_hsa_circ_183240,RMVar_hsa_circ_183237,RMVar_hsa_circ_183238,RMVar_hsa_circ_100848,RMVar_hsa_circ_183242 49932 RMVar_ID_49932 Human_SNP_ID_621648097 A-to-I Human chr17 + 30485518 30485518 30485518 CTCTAACTCCTGTGTTCACGAGGTTTTGCTATATTGCCCAGGCTGGTCTCTTAACTCCTGTGTTC CTCTAACTCCTGTGTTCACGAGGTTTTGCTATGTTGCCCAGGCTGGTCTCTTAACTCCTGTGTTC A G GOSR1 Ensembl:ENSG00000108587 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1455007556 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17565552 RMVar_hsa_circ_183234,RMVar_hsa_circ_108830,RMVar_hsa_circ_341664,RMVar_hsa_circ_277054,RMVar_hsa_circ_272577,RMVar_hsa_circ_183236,RMVar_hsa_circ_34147,RMVar_hsa_circ_183235,RMVar_hsa_circ_20676,RMVar_hsa_circ_183239,RMVar_hsa_circ_57502,RMVar_hsa_circ_293685,RMVar_hsa_circ_308977,RMVar_hsa_circ_270274,RMVar_hsa_circ_183240,RMVar_hsa_circ_183237,RMVar_hsa_circ_183238,RMVar_hsa_circ_100848,RMVar_hsa_circ_183242 49933 RMVar_ID_49933 Human_SNP_ID_621648325 A-to-I Human chr17 + 30486397 30486397 30486397 AAATTAGCGGGGCGTGGTGGTGGGTGCCTGTTATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAA AAATTAGCGGGGCGTGGTGGTGGGTGCCTGTTGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAA A G GOSR1 Ensembl:ENSG00000108587 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1377459764 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22585669 RMVar_hsa_circ_183234,RMVar_hsa_circ_108830,RMVar_hsa_circ_341664,RMVar_hsa_circ_277054,RMVar_hsa_circ_272577,RMVar_hsa_circ_183236,RMVar_hsa_circ_34147,RMVar_hsa_circ_183235,RMVar_hsa_circ_20676,RMVar_hsa_circ_183239,RMVar_hsa_circ_57502,RMVar_hsa_circ_293685,RMVar_hsa_circ_308977,RMVar_hsa_circ_270274,RMVar_hsa_circ_183240,RMVar_hsa_circ_183237,RMVar_hsa_circ_183238,RMVar_hsa_circ_100848,RMVar_hsa_circ_183242 49934 RMVar_ID_49934 Human_SNP_ID_621648684 A-to-I Human chr17 + 30487985 30487985 30487985 TTTAGTAGAGATGGGGTTTCATCATATTGATCAAGCTGGTCTTGAACTCCTGATGTCATGATCCA TTTAGTAGAGATGGGGTTTCATCATATTGATCGAGCTGGTCTTGAACTCCTGATGTCATGATCCA A G GOSR1 Ensembl:ENSG00000108587 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1016356789 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12954001 RMVar_hsa_circ_183234,RMVar_hsa_circ_108830,RMVar_hsa_circ_341664,RMVar_hsa_circ_277054,RMVar_hsa_circ_272577,RMVar_hsa_circ_183236,RMVar_hsa_circ_34147,RMVar_hsa_circ_183235,RMVar_hsa_circ_20676,RMVar_hsa_circ_183239,RMVar_hsa_circ_57502,RMVar_hsa_circ_293685,RMVar_hsa_circ_308977,RMVar_hsa_circ_270274,RMVar_hsa_circ_183240,RMVar_hsa_circ_183237,RMVar_hsa_circ_183238,RMVar_hsa_circ_100848,RMVar_hsa_circ_183242 49935 RMVar_ID_49935 Human_SNP_ID_621648685 A-to-I Human chr17 + 30487985 30487985 30487985 TTTAGTAGAGATGGGGTTTCATCATATTGATCAAGCTGGTCTTGAACTCCTGATGTCATGATCCA TTTAGTAGAGATGGGGTTTCATCATATTGATCTAGCTGGTCTTGAACTCCTGATGTCATGATCCA A T GOSR1 Ensembl:ENSG00000108587 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1016356789 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12954001 RMVar_hsa_circ_183234,RMVar_hsa_circ_108830,RMVar_hsa_circ_341664,RMVar_hsa_circ_277054,RMVar_hsa_circ_272577,RMVar_hsa_circ_183236,RMVar_hsa_circ_34147,RMVar_hsa_circ_183235,RMVar_hsa_circ_20676,RMVar_hsa_circ_183239,RMVar_hsa_circ_57502,RMVar_hsa_circ_293685,RMVar_hsa_circ_308977,RMVar_hsa_circ_270274,RMVar_hsa_circ_183240,RMVar_hsa_circ_183237,RMVar_hsa_circ_183238,RMVar_hsa_circ_100848,RMVar_hsa_circ_183242 49936 RMVar_ID_49936 Human_SNP_ID_621648864 A-to-I Human chr17 + 30488553 30488553 30488553 TTTATTGGCAGTATTTTTTTTTTTTTTTTTTGAAACAGAGTCTCGCTCTGTTGCCTAGGCTGGAG TTTATTGGCAGTATTTTTTTTTTTTTTTTTTGCAACAGAGTCTCGCTCTGTTGCCTAGGCTGGAG A C GOSR1 Ensembl:ENSG00000108587 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1489557969 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12954002 RMVar_hsa_circ_183234,RMVar_hsa_circ_108830,RMVar_hsa_circ_341664,RMVar_hsa_circ_277054,RMVar_hsa_circ_272577,RMVar_hsa_circ_183236,RMVar_hsa_circ_34147,RMVar_hsa_circ_183235,RMVar_hsa_circ_20676,RMVar_hsa_circ_183239,RMVar_hsa_circ_57502,RMVar_hsa_circ_293685,RMVar_hsa_circ_308977,RMVar_hsa_circ_270274,RMVar_hsa_circ_183240,RMVar_hsa_circ_183237,RMVar_hsa_circ_183238,RMVar_hsa_circ_100848,RMVar_hsa_circ_183242 49937 RMVar_ID_49937 Human_SNP_ID_621648865 A-to-I Human chr17 + 30488553 30488553 30488553 TTTATTGGCAGTATTTTTTTTTTTTTTTTTTGAAACAGAGTCTCGCTCTGTTGCCTAGGCTGGAG TTTATTGGCAGTATTTTTTTTTTTTTTTTTTGTAACAGAGTCTCGCTCTGTTGCCTAGGCTGGAG A T GOSR1 Ensembl:ENSG00000108587 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1489557969 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12954002 RMVar_hsa_circ_183234,RMVar_hsa_circ_108830,RMVar_hsa_circ_341664,RMVar_hsa_circ_277054,RMVar_hsa_circ_272577,RMVar_hsa_circ_183236,RMVar_hsa_circ_34147,RMVar_hsa_circ_183235,RMVar_hsa_circ_20676,RMVar_hsa_circ_183239,RMVar_hsa_circ_57502,RMVar_hsa_circ_293685,RMVar_hsa_circ_308977,RMVar_hsa_circ_270274,RMVar_hsa_circ_183240,RMVar_hsa_circ_183237,RMVar_hsa_circ_183238,RMVar_hsa_circ_100848,RMVar_hsa_circ_183242 49938 RMVar_ID_49938 Human_SNP_ID_621650230 A-to-I Human chr17 + 30494677 30494677 30494677 TTGCCCAGGCTGGAGTGTCGCGGTGTGATCTCAGCTCACTGTGCCCTCTGCCTCCTGGGTTCCAG TTGCCCAGGCTGGAGTGTCGCGGTGTGATCTCGGCTCACTGTGCCCTCTGCCTCCTGGGTTCCAG A G GOSR1 Ensembl:ENSG00000108587 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs899215182 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108830,RMVar_hsa_circ_341664,RMVar_hsa_circ_183236,RMVar_hsa_circ_34147,RMVar_hsa_circ_57502,RMVar_hsa_circ_293685,RMVar_hsa_circ_308977,RMVar_hsa_circ_183237,RMVar_hsa_circ_183238,RMVar_hsa_circ_100848,RMVar_hsa_circ_183243,RMVar_hsa_circ_183242 49939 RMVar_ID_49939 Human_SNP_ID_621652611 A-to-I Human chr17 + 30505296 30505296 30505296 GTGGCTTATGCCTGTGATTCCAGTTACTTGGGAGGCTGAGGCAGGAGGATTGCTTGAAGCCCAGA GTGGCTTATGCCTGTGATTCCAGTTACTTGGGGGGCTGAGGCAGGAGGATTGCTTGAAGCCCAGA A G GOSR1 Ensembl:ENSG00000108587 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1357460837 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17888903,Human_RBP_ID_25339686 RMVar_hsa_circ_108830,RMVar_hsa_circ_341664,RMVar_hsa_circ_183236,RMVar_hsa_circ_293685,RMVar_hsa_circ_308977,RMVar_hsa_circ_183237,RMVar_hsa_circ_183238,RMVar_hsa_circ_100848,RMVar_hsa_circ_183243,RMVar_hsa_circ_183242 49940 RMVar_ID_49940 Human_SNP_ID_621653615 A-to-I Human chr17 + 30510107 30510107 30510107 TTTGGAGTTTTTTTGAGACAGAGTCTTGCTCTATGGCCCAGGCTGGAGTGCAGTGGCATGATGAT TTTGGAGTTTTTTTGAGACAGAGTCTTGCTCTGTGGCCCAGGCTGGAGTGCAGTGGCATGATGAT A G GOSR1 Ensembl:ENSG00000108587 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs527661822 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108830,RMVar_hsa_circ_341664,RMVar_hsa_circ_183236,RMVar_hsa_circ_293685,RMVar_hsa_circ_308977,RMVar_hsa_circ_183237,RMVar_hsa_circ_183238,RMVar_hsa_circ_100848,RMVar_hsa_circ_183243,RMVar_hsa_circ_183242 49941 RMVar_ID_49941 Human_SNP_ID_621682608 A-to-I Human chr17 + 30633274 30633274 30633274 TGTCGCGAACAGGCCTCCTGATGAAGCTTCTCAGCGAGCAGCAGGAAGCAAAGGCATTGAATGTA TGTCGCGAACAGGCCTCCTGATGAAGCTTCTCGGCGAGCAGCAGGAAGCAAAGGCATTGAATGTA A G AC005562.1,LRRC37BP1 Ensembl:ENSG00000214719,Ensembl:ENSG00000250462 lincRNA,Pseudogene exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1460457914 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1865285,Human_miRNA_ID_1907338,Human_miRNA_ID_2512915,Human_miRNA_ID_2512916,Human_miRNA_ID_3055738,Human_miRNA_ID_3055739,Human_miRNA_ID_3179972,Human_miRNA_ID_3212426 RMVar_hsa_circ_93203,RMVar_hsa_circ_329473,RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_61760,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_183249 49942 RMVar_ID_49942 Human_SNP_ID_621683327 A-to-I Human chr17 - 30635620 30635620 30635620 CAGGCTAGAGTGCAGTGGTATGACCACAGCTCACTGCATCCTCGACCTCCCAGGCTCAAGCAATC CAGGCTAGAGTGCAGTGGTATGACCACAGCTCGCTGCATCCTCGACCTCCCAGGCTCAAGCAATC T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs557797605 Functional Loss SNV dbSNP153 33..33 33 - - - 49943 RMVar_ID_49943 Human_SNP_ID_621683484 A-to-I Human chr17 + 30636278 30636278 30636278 AAACTCCTGGGCTTAAGGGATCCTCCTGCCTCAGCTTCCTGAGTGGCTGGGACTACAGGCAGGCA AAACTCCTGGGCTTAAGGGATCCTCCTGCCTCGGCTTCCTGAGTGGCTGGGACTACAGGCAGGCA A G AC005562.1,LRRC37BP1 Ensembl:ENSG00000214719,Ensembl:ENSG00000250462 lincRNA,Pseudogene intron,intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1237306230 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247 49944 RMVar_ID_49944 Human_SNP_ID_621683627 A-to-I Human chr17 + 30636814 30636814 30636814 GTGGTGGTATGCACCTGTAGTCCCAGCTACTCAAGAGGCTGAGGTGGGCAGATCACTGGAGCCCA GTGGTGGTATGCACCTGTAGTCCCAGCTACTCGAGAGGCTGAGGTGGGCAGATCACTGGAGCCCA A G AC005562.1,LRRC37BP1 Ensembl:ENSG00000214719,Ensembl:ENSG00000250462 lincRNA,Pseudogene intron,intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1162313555 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247 49945 RMVar_ID_49945 Human_SNP_ID_621705662 A-to-I Human chr17 + 30720698 30720698 30720698 AGGCGGGGGTTTGTGTGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGCTGGGAGGATCACTTGAG AGGCGGGGGTTTGTGTGCCTGTAGTCCCAGCTGCTCAGGAGGCTGAGCTGGGAGGATCACTTGAG A G SUZ12P1 Ensembl:ENSG00000264538 Pseudogene intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1162094732 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247 49946 RMVar_ID_49946 Human_SNP_ID_621706319 A-to-I Human chr17 + 30723804 30723804 30723804 CCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGAGGATCGCTTGAGGCCAGGAGCTCAAGACC CCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGAGGATCGCTTGAGGCCAGGAGCTCAAGACC A G SUZ12P1 Ensembl:ENSG00000264538 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs564027901 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247 49947 RMVar_ID_49947 Human_SNP_ID_621706324 A-to-I Human chr17 + 30723831 30723831 30723831 AAGGCAGGAGGATCGCTTGAGGCCAGGAGCTCAAGACCAGCCTGGGCAACATAGTGAGACCCCAT AAGGCAGGAGGATCGCTTGAGGCCAGGAGCTCCAGACCAGCCTGGGCAACATAGTGAGACCCCAT A C SUZ12P1 Ensembl:ENSG00000264538 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs947159483 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247 49948 RMVar_ID_49948 Human_SNP_ID_621706325 A-to-I Human chr17 + 30723831 30723831 30723831 AAGGCAGGAGGATCGCTTGAGGCCAGGAGCTCAAGACCAGCCTGGGCAACATAGTGAGACCCCAT AAGGCAGGAGGATCGCTTGAGGCCAGGAGCTCGAGACCAGCCTGGGCAACATAGTGAGACCCCAT A G SUZ12P1 Ensembl:ENSG00000264538 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs947159483 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247 49949 RMVar_ID_49949 Human_SNP_ID_621706326 A-to-I Human chr17 + 30723831 30723831 30723831 AAGGCAGGAGGATCGCTTGAGGCCAGGAGCTCAAGACCAGCCTGGGCAACATAGTGAGACCCCAT AAGGCAGGAGGATCGCTTGAGGCCAGGAGCTCTAGACCAGCCTGGGCAACATAGTGAGACCCCAT A T SUZ12P1 Ensembl:ENSG00000264538 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs947159483 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247 49950 RMVar_ID_49950 Human_SNP_ID_621709766 A-to-I Human chr17 + 30735599 30735599 30735599 AGATTGCGCCGTTGCACTTCAGCCTGGGCAACAGAGCGAGACTCTACCTCAAAGAAAAAAAAAAA AGATTGCGCCGTTGCACTTCAGCCTGGGCAACGGAGCGAGACTCTACCTCAAAGAAAAAAAAAAA A G SUZ12P1 Ensembl:ENSG00000264538 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1185464926 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8254252,Human_RBP_ID_12955376,Human_RBP_ID_18514220,Human_RBP_ID_25339753,Human_RBP_ID_26758262 RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_293925,RMVar_hsa_circ_312765,RMVar_hsa_circ_303849,RMVar_hsa_circ_278172,RMVar_hsa_circ_126507,RMVar_hsa_circ_270645,RMVar_hsa_circ_274224,RMVar_hsa_circ_265220,RMVar_hsa_circ_313317,RMVar_hsa_circ_183256,RMVar_hsa_circ_183258,RMVar_hsa_circ_183259,RMVar_hsa_circ_183257,RMVar_hsa_circ_355423,RMVar_hsa_circ_364780,RMVar_hsa_circ_359681,RMVar_hsa_circ_344773 49951 RMVar_ID_49951 Human_SNP_ID_621710323 A-to-I Human chr17 + 30736983 30736983 30736983 AAGTCTCACTCTTGTCCCCCAGGCTGGAGTGTAATGGTGCAATCTCGGCTCACTGTGACCTCTGT AAGTCTCACTCTTGTCCCCCAGGCTGGAGTGTCATGGTGCAATCTCGGCTCACTGTGACCTCTGT A C SUZ12P1 Ensembl:ENSG00000264538 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1243958965 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13219795 RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_293925,RMVar_hsa_circ_312765,RMVar_hsa_circ_303849,RMVar_hsa_circ_278172,RMVar_hsa_circ_126507,RMVar_hsa_circ_270645,RMVar_hsa_circ_274224,RMVar_hsa_circ_265220,RMVar_hsa_circ_313317,RMVar_hsa_circ_183256,RMVar_hsa_circ_183258,RMVar_hsa_circ_183259,RMVar_hsa_circ_183257,RMVar_hsa_circ_355423,RMVar_hsa_circ_364780,RMVar_hsa_circ_359681,RMVar_hsa_circ_344773 49952 RMVar_ID_49952 Human_SNP_ID_621710443 A-to-I Human chr17 + 30737293 30737293 30737293 CAGGCTGGAGTGCAGTGGCGCAACCTCGGCTCACTGCTACCTCCGCCTCCCAGATTCAAGAGATT CAGGCTGGAGTGCAGTGGCGCAACCTCGGCTCCCTGCTACCTCCGCCTCCCAGATTCAAGAGATT A C SUZ12P1 Ensembl:ENSG00000264538 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1371841467 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12955405,Human_RBP_ID_18514222 RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_293925,RMVar_hsa_circ_312765,RMVar_hsa_circ_303849,RMVar_hsa_circ_278172,RMVar_hsa_circ_126507,RMVar_hsa_circ_270645,RMVar_hsa_circ_274224,RMVar_hsa_circ_265220,RMVar_hsa_circ_313317,RMVar_hsa_circ_183256,RMVar_hsa_circ_183258,RMVar_hsa_circ_183259,RMVar_hsa_circ_183257,RMVar_hsa_circ_355423,RMVar_hsa_circ_364780,RMVar_hsa_circ_359681,RMVar_hsa_circ_344773 49953 RMVar_ID_49953 Human_SNP_ID_621710477 A-to-I Human chr17 + 30737358 30737358 30737358 CTCCTGCTTCAGCCTCCCGAGTAGCTTGGACTATAGGCGCGTGCCACCATGCTCGGCTAATTTTT CTCCTGCTTCAGCCTCCCGAGTAGCTTGGACTGTAGGCGCGTGCCACCATGCTCGGCTAATTTTT A G SUZ12P1 Ensembl:ENSG00000264538 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs970605610 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12955409,Human_RBP_ID_17378872 RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_293925,RMVar_hsa_circ_312765,RMVar_hsa_circ_303849,RMVar_hsa_circ_278172,RMVar_hsa_circ_126507,RMVar_hsa_circ_270645,RMVar_hsa_circ_274224,RMVar_hsa_circ_265220,RMVar_hsa_circ_313317,RMVar_hsa_circ_183256,RMVar_hsa_circ_183258,RMVar_hsa_circ_183259,RMVar_hsa_circ_183257,RMVar_hsa_circ_355423,RMVar_hsa_circ_364780,RMVar_hsa_circ_359681,RMVar_hsa_circ_344773 49954 RMVar_ID_49954 Human_SNP_ID_621712142 A-to-I Human chr17 + 30743299 30743299 30743299 AGAAGTGATTATTTTGTTTATCTGTTTCTTCCAGGAAAACATTTAAAGTTGATGATATGTTATCA AGAAGTGATTATTTTGTTTATCTGTTTCTTCCGGGAAAACATTTAAAGTTGATGATATGTTATCA A G SUZ12P1 Ensembl:ENSG00000264538 Pseudogene intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1470651537 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22656087 Human_Splice_Rec_1800693,Human_Splice_Rec_1800707,Human_Splice_Rec_1800721,Human_Splice_Rec_1800729,Human_Splice_Rec_1800743 RMVar_hsa_circ_55435,RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_293925,RMVar_hsa_circ_312765,RMVar_hsa_circ_303849,RMVar_hsa_circ_278172,RMVar_hsa_circ_126507,RMVar_hsa_circ_270645,RMVar_hsa_circ_274224,RMVar_hsa_circ_265220,RMVar_hsa_circ_313317,RMVar_hsa_circ_183256,RMVar_hsa_circ_183258,RMVar_hsa_circ_183259,RMVar_hsa_circ_183257,RMVar_hsa_circ_355423,RMVar_hsa_circ_364780,RMVar_hsa_circ_359681,RMVar_hsa_circ_344773,RMVar_hsa_circ_302491,RMVar_hsa_circ_304580,RMVar_hsa_circ_275624 49955 RMVar_ID_49955 Human_SNP_ID_621713459 A-to-I Human chr17 + 30747924 30747924 30747924 CCACCATGCCTGGCTAATTTTTAAATTTTCGTAGAGGCAGCATCTTGCTATGTTGCCCAGGCTGG CCACCATGCCTGGCTAATTTTTAAATTTTCGTGGAGGCAGCATCTTGCTATGTTGCCCAGGCTGG A G SUZ12P1 Ensembl:ENSG00000264538 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs565557361 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6578869,Human_RBP_ID_12955762 RMVar_hsa_circ_55435,RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_293925,RMVar_hsa_circ_312765,RMVar_hsa_circ_278172,RMVar_hsa_circ_126507,RMVar_hsa_circ_270645,RMVar_hsa_circ_274224,RMVar_hsa_circ_265220,RMVar_hsa_circ_183258,RMVar_hsa_circ_183259,RMVar_hsa_circ_183257,RMVar_hsa_circ_355423,RMVar_hsa_circ_364780,RMVar_hsa_circ_359681,RMVar_hsa_circ_344773,RMVar_hsa_circ_302491,RMVar_hsa_circ_304580,RMVar_hsa_circ_275624 49956 RMVar_ID_49956 Human_SNP_ID_621713460 A-to-I Human chr17 + 30747924 30747924 30747924 CCACCATGCCTGGCTAATTTTTAAATTTTCGTAGAGGCAGCATCTTGCTATGTTGCCCAGGCTGG CCACCATGCCTGGCTAATTTTTAAATTTTCGTTGAGGCAGCATCTTGCTATGTTGCCCAGGCTGG A T SUZ12P1 Ensembl:ENSG00000264538 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs565557361 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6578869,Human_RBP_ID_12955762 RMVar_hsa_circ_55435,RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_293925,RMVar_hsa_circ_312765,RMVar_hsa_circ_278172,RMVar_hsa_circ_126507,RMVar_hsa_circ_270645,RMVar_hsa_circ_274224,RMVar_hsa_circ_265220,RMVar_hsa_circ_183258,RMVar_hsa_circ_183259,RMVar_hsa_circ_183257,RMVar_hsa_circ_355423,RMVar_hsa_circ_364780,RMVar_hsa_circ_359681,RMVar_hsa_circ_344773,RMVar_hsa_circ_302491,RMVar_hsa_circ_304580,RMVar_hsa_circ_275624 49957 RMVar_ID_49957 Human_SNP_ID_621713623 A-to-I Human chr17 + 30748422 30748422 30748422 GCCCAGCTACTTTCTGTATTTTTAATAGAGACAGGGTTTTACCATGTTGGTCAGGCTGGTCTTGA GCCCAGCTACTTTCTGTATTTTTAATAGAGACCGGGTTTTACCATGTTGGTCAGGCTGGTCTTGA A C SUZ12P1 Ensembl:ENSG00000264538 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs536844829 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55435,RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_293925,RMVar_hsa_circ_312765,RMVar_hsa_circ_278172,RMVar_hsa_circ_126507,RMVar_hsa_circ_270645,RMVar_hsa_circ_274224,RMVar_hsa_circ_265220,RMVar_hsa_circ_183258,RMVar_hsa_circ_183259,RMVar_hsa_circ_183257,RMVar_hsa_circ_355423,RMVar_hsa_circ_364780,RMVar_hsa_circ_359681,RMVar_hsa_circ_344773,RMVar_hsa_circ_302491,RMVar_hsa_circ_304580,RMVar_hsa_circ_275624 49958 RMVar_ID_49958 Human_SNP_ID_621716440 A-to-I Human chr17 + 30756803 30756803 30756803 GAGAATGGCTTGAACCCTGGGAGGCAGAAGTTACAGTGAGCCAAGATCACACCATTGAACTCCAG GAGAATGGCTTGAACCCTGGGAGGCAGAAGTTGCAGTGAGCCAAGATCACACCATTGAACTCCAG A G SUZ12P1 Ensembl:ENSG00000264538 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1313706807 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8254275,Human_RBP_ID_12956052,Human_RBP_ID_17379870,Human_RBP_ID_18514264,Human_RBP_ID_18531413,Human_RBP_ID_23168263,Human_RBP_ID_25339809 RMVar_hsa_circ_55435,RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_293925,RMVar_hsa_circ_312765,RMVar_hsa_circ_278172,RMVar_hsa_circ_126507,RMVar_hsa_circ_270645,RMVar_hsa_circ_274224,RMVar_hsa_circ_265220,RMVar_hsa_circ_183258,RMVar_hsa_circ_183259,RMVar_hsa_circ_183257,RMVar_hsa_circ_355423,RMVar_hsa_circ_364780,RMVar_hsa_circ_359681,RMVar_hsa_circ_344773,RMVar_hsa_circ_302491,RMVar_hsa_circ_304580,RMVar_hsa_circ_275624 49959 RMVar_ID_49959 Human_SNP_ID_621716717 A-to-I Human chr17 + 30757851 30757851 30757851 GCAGTCTCGGCTCACTGTAACCTCTGCCTCCTAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTG GCAGTCTCGGCTCACTGTAACCTCTGCCTCCTGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTG A G SUZ12P1 Ensembl:ENSG00000264538 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350356572 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17379594 RMVar_hsa_circ_55435,RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_293925,RMVar_hsa_circ_312765,RMVar_hsa_circ_278172,RMVar_hsa_circ_126507,RMVar_hsa_circ_270645,RMVar_hsa_circ_274224,RMVar_hsa_circ_265220,RMVar_hsa_circ_183258,RMVar_hsa_circ_183259,RMVar_hsa_circ_183257,RMVar_hsa_circ_355423,RMVar_hsa_circ_364780,RMVar_hsa_circ_359681,RMVar_hsa_circ_344773,RMVar_hsa_circ_302491,RMVar_hsa_circ_304580,RMVar_hsa_circ_275624 49960 RMVar_ID_49960 Human_SNP_ID_621717360 A-to-I Human chr17 + 30760309 30760309 30760309 AGTGGCTCATGCCTGTAATCCCAACATTTTGGAAGGCTGAGGCGGGTGTATCATGAGGCCAGGAG AGTGGCTCATGCCTGTAATCCCAACATTTTGGGAGGCTGAGGCGGGTGTATCATGAGGCCAGGAG A G SUZ12P1 Ensembl:ENSG00000264538 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1352322171 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55435,RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_293925,RMVar_hsa_circ_312765,RMVar_hsa_circ_278172,RMVar_hsa_circ_126507,RMVar_hsa_circ_270645,RMVar_hsa_circ_265220,RMVar_hsa_circ_183258,RMVar_hsa_circ_183259,RMVar_hsa_circ_183257,RMVar_hsa_circ_364780,RMVar_hsa_circ_359681,RMVar_hsa_circ_344773,RMVar_hsa_circ_304580,RMVar_hsa_circ_275624,RMVar_hsa_circ_271659,RMVar_hsa_circ_309967 49961 RMVar_ID_49961 Human_SNP_ID_621717399 A-to-I Human chr17 + 30760473 30760473 30760473 GGAGACTTAGGCAGAAGAATCGCTTGAACCTGAGAGTCAGAGGTTGCAGTGAGCTGAGATTGTGT GGAGACTTAGGCAGAAGAATCGCTTGAACCTGCGAGTCAGAGGTTGCAGTGAGCTGAGATTGTGT A C SUZ12P1 Ensembl:ENSG00000264538 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1303780176 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55435,RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_293925,RMVar_hsa_circ_312765,RMVar_hsa_circ_278172,RMVar_hsa_circ_126507,RMVar_hsa_circ_270645,RMVar_hsa_circ_265220,RMVar_hsa_circ_183258,RMVar_hsa_circ_183259,RMVar_hsa_circ_183257,RMVar_hsa_circ_364780,RMVar_hsa_circ_359681,RMVar_hsa_circ_344773,RMVar_hsa_circ_304580,RMVar_hsa_circ_275624,RMVar_hsa_circ_271659,RMVar_hsa_circ_309967 49962 RMVar_ID_49962 Human_SNP_ID_621718043 A-to-I Human chr17 + 30762509 30762509 30762509 CTCAGATCACTGCAGCCTCTGCCTCCAGGTTCAAGTAATTCTCATGCCTCAGCCTCCCAAGTATC CTCAGATCACTGCAGCCTCTGCCTCCAGGTTCTAGTAATTCTCATGCCTCAGCCTCCCAAGTATC A T SUZ12P1 Ensembl:ENSG00000264538 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1178681329 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8254851,Human_RBP_ID_18514274 RMVar_hsa_circ_55435,RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_293925,RMVar_hsa_circ_312765,RMVar_hsa_circ_278172,RMVar_hsa_circ_126507,RMVar_hsa_circ_270645,RMVar_hsa_circ_265220,RMVar_hsa_circ_183258,RMVar_hsa_circ_183259,RMVar_hsa_circ_183257,RMVar_hsa_circ_364780,RMVar_hsa_circ_359681,RMVar_hsa_circ_344773,RMVar_hsa_circ_304580,RMVar_hsa_circ_275624,RMVar_hsa_circ_271659,RMVar_hsa_circ_309967 49963 RMVar_ID_49963 Human_SNP_ID_621718045 A-to-I Human chr17 + 30762513 30762513 30762513 GATCACTGCAGCCTCTGCCTCCAGGTTCAAGTAATTCTCATGCCTCAGCCTCCCAAGTATCTGGG GATCACTGCAGCCTCTGCCTCCAGGTTCAAGTGATTCTCATGCCTCAGCCTCCCAAGTATCTGGG A G SUZ12P1 Ensembl:ENSG00000264538 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1327156189 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8254851,Human_RBP_ID_18514274 RMVar_hsa_circ_55435,RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_293925,RMVar_hsa_circ_312765,RMVar_hsa_circ_278172,RMVar_hsa_circ_126507,RMVar_hsa_circ_270645,RMVar_hsa_circ_265220,RMVar_hsa_circ_183258,RMVar_hsa_circ_183259,RMVar_hsa_circ_183257,RMVar_hsa_circ_364780,RMVar_hsa_circ_359681,RMVar_hsa_circ_344773,RMVar_hsa_circ_304580,RMVar_hsa_circ_275624,RMVar_hsa_circ_271659,RMVar_hsa_circ_309967 49964 RMVar_ID_49964 Human_SNP_ID_621719045 A-to-I Human chr17 + 30765818 30765818 30765818 TAGAGACAGGATCTCACTCTTTCGCCCAGACTAGAGGGCAGTGACAGGATCATAGCTCACTGCAG TAGAGACAGGATCTCACTCTTTCGCCCAGACTGGAGGGCAGTGACAGGATCATAGCTCACTGCAG A G SUZ12P1 Ensembl:ENSG00000264538 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1289521922 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55435,RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_293925,RMVar_hsa_circ_312765,RMVar_hsa_circ_278172,RMVar_hsa_circ_126507,RMVar_hsa_circ_270645,RMVar_hsa_circ_265220,RMVar_hsa_circ_183258,RMVar_hsa_circ_183259,RMVar_hsa_circ_183257,RMVar_hsa_circ_364780,RMVar_hsa_circ_359681,RMVar_hsa_circ_344773,RMVar_hsa_circ_304580,RMVar_hsa_circ_275624,RMVar_hsa_circ_271659,RMVar_hsa_circ_309967 49965 RMVar_ID_49965 Human_SNP_ID_621720398 A-to-I Human chr17 + 30770765 30770765 30770765 CTCCTGCTTTAGCCTCTGGAGTAGCTGGGACTACAAGTGCGTGCCACCACGCCCGGCTAATTTTT CTCCTGCTTTAGCCTCTGGAGTAGCTGGGACTTCAAGTGCGTGCCACCACGCCCGGCTAATTTTT A T SUZ12P1 Ensembl:ENSG00000264538 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1201057108 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55435,RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_293925,RMVar_hsa_circ_68200,RMVar_hsa_circ_183260 49966 RMVar_ID_49966 Human_SNP_ID_621720506 A-to-I Human chr17 + 30771018 30771018 30771018 TCAGCTCTTTGGGAGGCTGAAGCGGGTGGATCACGAGGTCAGGAGTTTGAGACCAGCCTGGCCAA TCAGCTCTTTGGGAGGCTGAAGCGGGTGGATCCCGAGGTCAGGAGTTTGAGACCAGCCTGGCCAA A C SUZ12P1 Ensembl:ENSG00000264538 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1480919082 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17379610 RMVar_hsa_circ_55435,RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_293925,RMVar_hsa_circ_68200,RMVar_hsa_circ_183260 49967 RMVar_ID_49967 Human_SNP_ID_621720772 A-to-I Human chr17 + 30771732 30771732 30771732 CGCTACCATGCCCAGCTAATTTTTGTGTTTTTAGAGAGATGAGGTTTCACCATGTTGGCCAGGCT CGCTACCATGCCCAGCTAATTTTTGTGTTTTTGGAGAGATGAGGTTTCACCATGTTGGCCAGGCT A G SUZ12P1 Ensembl:ENSG00000264538 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1230084947 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8254856,Human_RBP_ID_17380266,Human_RBP_ID_22948966,Human_RBP_ID_25339849 RMVar_hsa_circ_55435,RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_293925,RMVar_hsa_circ_68200,RMVar_hsa_circ_183260 49968 RMVar_ID_49968 Human_SNP_ID_621721681 A-to-I Human chr17 + 30774013 30774013 30774013 GTTGGTCAGGCTGGTCTTGAACTCCCGACCTCAGGTGATCCTCCCACCTCAGCCTCCCGAAGTGT GTTGGTCAGGCTGGTCTTGAACTCCCGACCTCGGGTGATCCTCCCACCTCAGCCTCCCGAAGTGT A G SUZ12P1 Ensembl:ENSG00000264538 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1211646696 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55435,RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_293925,RMVar_hsa_circ_68200,RMVar_hsa_circ_183260 49969 RMVar_ID_49969 Human_SNP_ID_621722259 A-to-I Human chr17 + 30775863 30775863 30775863 CGCGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCTGGGCAGCAGA CGCGCCTGTAATCCCAGCTACTCGGGAGGCTGGGGCAGGAGAATCGCTTGAACCTGGGCAGCAGA A G SUZ12P1 Ensembl:ENSG00000264538 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1182074519 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55435,RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_293925,RMVar_hsa_circ_68200,RMVar_hsa_circ_183260 49970 RMVar_ID_49970 Human_SNP_ID_621722554 A-to-I Human chr17 + 30776739 30776739 30776739 GTGATTACAGGTGCGTGCCACCACGCCTGGCTAATTTGTTTTATTTTCAGTAGAGACGGGGTTTG GTGATTACAGGTGCGTGCCACCACGCCTGGCTGATTTGTTTTATTTTCAGTAGAGACGGGGTTTG A G SUZ12P1 Ensembl:ENSG00000264538 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs538131807 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12956413 RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_293925,RMVar_hsa_circ_68200,RMVar_hsa_circ_183260 49971 RMVar_ID_49971 Human_SNP_ID_621723100 A-to-I Human chr17 - 30778381 30778377 30778382 AGAGTCTTGCTCTGTCTCCCCGGATAAAGTGAAGTGGCAAAATCTCAGCTCACTGAAACCTCTGC AGAGTCTTGCTCTGTCTCCCCGGATAAAGTG_____GCAAAATCTCAGCTCACTGAAACCTCTGC CCACTT C CRLF3 Ensembl:ENSG00000176390 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1339231653 Functional Loss DEL dbSNP153 32..36 33 - - - 49972 RMVar_ID_49972 Human_SNP_ID_621723720 A-to-I Human chr17 + 30780065 30780065 30780065 TGCCGGCCTCGGCCTCCCAAAGTGCTGGGATTACATGCGTGAGCCACTGTGCCTGGCCATTTATT TGCCGGCCTCGGCCTCCCAAAGTGCTGGGATTGCATGCGTGAGCCACTGTGCCTGGCCATTTATT A G SUZ12P1 Ensembl:ENSG00000264538 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879466666 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_293925,RMVar_hsa_circ_68200,RMVar_hsa_circ_183260 49973 RMVar_ID_49973 Human_SNP_ID_621723749 A-to-I Human chr17 + 30780160 30780160 30780160 CCAGCTCGCTGTAGCCTCAAGCTCCTGAACTCAAGTGATCCTCCCACCTTAGCCTCCTGAGTAGC CCAGCTCGCTGTAGCCTCAAGCTCCTGAACTCCAGTGATCCTCCCACCTTAGCCTCCTGAGTAGC A C SUZ12P1 Ensembl:ENSG00000264538 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1049173621 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5247979,Human_RBP_ID_12956521 RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_293925,RMVar_hsa_circ_68200,RMVar_hsa_circ_183260 49974 RMVar_ID_49974 Human_SNP_ID_621724043 A-to-I Human chr17 + 30780942 30780923 30780942 CCCACCTCAGTCTCCTGAGTAGCTTTGGAACTACTGGTGGGCACCACAACACCTGGCTAAATTTT CCCACCTCAGTCTC___________________CTGGTGGGCACCACAACACCTGGCTAAATTTT CCTGAGTAGCTTTGGAACTA C SUZ12P1 Ensembl:ENSG00000264538 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1327101920 Functional Loss DEL dbSNP153 15..33 33 - - - Human_RBP_ID_6579092,Human_RBP_ID_12956563 RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_293925,RMVar_hsa_circ_183261,RMVar_hsa_circ_68200,RMVar_hsa_circ_183260 49975 RMVar_ID_49975 Human_SNP_ID_621724132 A-to-I Human chr17 + 30781082 30781082 30781082 CTGACTGCAGCCTCCACCCCCCGAGTTCAAGCAATTCTCCTGCCTCAGCCTCCCATGTGGCTGGG CTGACTGCAGCCTCCACCCCCCGAGTTCAAGCCATTCTCCTGCCTCAGCCTCCCATGTGGCTGGG A C SUZ12P1 Ensembl:ENSG00000264538 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs72811650 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12956572 GWAS_ID_6151,GWAS_ID_6152,GWAS_ID_6153,GWAS_ID_6154,GWAS_ID_6155,GWAS_ID_6156,GWAS_ID_6157,GWAS_ID_6158,GWAS_ID_6159,GWAS_ID_6160,GWAS_ID_6161,GWAS_ID_6162,GWAS_ID_6163,GWAS_ID_6164,GWAS_ID_6165,GWAS_ID_6166,GWAS_ID_6167,GWAS_ID_6168,GWAS_ID_6169,GWAS_ID_6170,GWAS_ID_6171,GWAS_ID_6172,GWAS_ID_6173,GWAS_ID_6174,GWAS_ID_6175,GWAS_ID_6176,GWAS_ID_6177,GWAS_ID_6178,GWAS_ID_6179,GWAS_ID_6180,GWAS_ID_6181,GWAS_ID_6182,GWAS_ID_6183,GWAS_ID_6184,GWAS_ID_6185,GWAS_ID_6186,GWAS_ID_6187,GWAS_ID_6188,GWAS_ID_6189,GWAS_ID_6190,GWAS_ID_6191,GWAS_ID_6192,GWAS_ID_6193,GWAS_ID_6194,GWAS_ID_6195,GWAS_ID_6196,GWAS_ID_6197,GWAS_ID_6198,GWAS_ID_6199,GWAS_ID_6200,GWAS_ID_6201,GWAS_ID_6202,GWAS_ID_6203,GWAS_ID_6204,GWAS_ID_6205,GWAS_ID_6206,GWAS_ID_6207,GWAS_ID_6208,GWAS_ID_6209,GWAS_ID_6210,GWAS_ID_6211,GWAS_ID_6212,GWAS_ID_6213,GWAS_ID_6214,GWAS_ID_6215,GWAS_ID_6216,GWAS_ID_6217,GWAS_ID_6218,GWAS_ID_6219,GWAS_ID_6220,GWAS_ID_6221,GWAS_ID_6222,GWAS_ID_6223,GWAS_ID_6224,GWAS_ID_6225,GWAS_ID_6226,GWAS_ID_6227,GWAS_ID_6228,GWAS_ID_6229,GWAS_ID_6230,GWAS_ID_6231,GWAS_ID_6232,GWAS_ID_6233,GWAS_ID_6234,GWAS_ID_6235,GWAS_ID_6236,GWAS_ID_6237,GWAS_ID_6238,GWAS_ID_6239,GWAS_ID_6240,GWAS_ID_6241,GWAS_ID_6242,GWAS_ID_6243,GWAS_ID_6244,GWAS_ID_6245,GWAS_ID_6246,GWAS_ID_6247,GWAS_ID_6248,GWAS_ID_6249,GWAS_ID_6250,GWAS_ID_6251,GWAS_ID_6252,GWAS_ID_6253,GWAS_ID_6254,GWAS_ID_6255,GWAS_ID_6256,GWAS_ID_6257,GWAS_ID_6258,GWAS_ID_6259,GWAS_ID_6260,GWAS_ID_6261,GWAS_ID_6262,GWAS_ID_6263,GWAS_ID_6264,GWAS_ID_6265,GWAS_ID_6266,GWAS_ID_6267,GWAS_ID_6268,GWAS_ID_6269,GWAS_ID_6270,GWAS_ID_6271,GWAS_ID_6272,GWAS_ID_6273,GWAS_ID_6274,GWAS_ID_6275,GWAS_ID_6276,GWAS_ID_6277,GWAS_ID_6278,GWAS_ID_6279,GWAS_ID_6280,GWAS_ID_6281,GWAS_ID_6282,GWAS_ID_6283,GWAS_ID_6284,GWAS_ID_6285,GWAS_ID_6286,GWAS_ID_6287,GWAS_ID_6288,GWAS_ID_6289,GWAS_ID_6290,GWAS_ID_6291,GWAS_ID_6292,GWAS_ID_6293,GWAS_ID_6294,GWAS_ID_6295,GWAS_ID_6296,GWAS_ID_6297,GWAS_ID_6298,GWAS_ID_6299,GWAS_ID_6300,GWAS_ID_6301,GWAS_ID_6302,GWAS_ID_6303,GWAS_ID_6304,GWAS_ID_6305,GWAS_ID_6306,GWAS_ID_6307,GWAS_ID_6308,GWAS_ID_6309,GWAS_ID_6310,GWAS_ID_6311,GWAS_ID_6312,GWAS_ID_6313,GWAS_ID_6314,GWAS_ID_6315,GWAS_ID_6316,GWAS_ID_6317,GWAS_ID_6318,GWAS_ID_6319,GWAS_ID_6320,GWAS_ID_6321,GWAS_ID_6322,GWAS_ID_6323,GWAS_ID_6324,GWAS_ID_6325,GWAS_ID_6326,GWAS_ID_6327 RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_293925,RMVar_hsa_circ_183261,RMVar_hsa_circ_68200,RMVar_hsa_circ_183260 49976 RMVar_ID_49976 Human_SNP_ID_621724133 A-to-I Human chr17 + 30781082 30781082 30781082 CTGACTGCAGCCTCCACCCCCCGAGTTCAAGCAATTCTCCTGCCTCAGCCTCCCATGTGGCTGGG CTGACTGCAGCCTCCACCCCCCGAGTTCAAGCGATTCTCCTGCCTCAGCCTCCCATGTGGCTGGG A G SUZ12P1 Ensembl:ENSG00000264538 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs72811650 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12956572 GWAS_ID_6151,GWAS_ID_6152,GWAS_ID_6153,GWAS_ID_6154,GWAS_ID_6155,GWAS_ID_6156,GWAS_ID_6157,GWAS_ID_6158,GWAS_ID_6159,GWAS_ID_6160,GWAS_ID_6161,GWAS_ID_6162,GWAS_ID_6163,GWAS_ID_6164,GWAS_ID_6165,GWAS_ID_6166,GWAS_ID_6167,GWAS_ID_6168,GWAS_ID_6169,GWAS_ID_6170,GWAS_ID_6171,GWAS_ID_6172,GWAS_ID_6173,GWAS_ID_6174,GWAS_ID_6175,GWAS_ID_6176,GWAS_ID_6177,GWAS_ID_6178,GWAS_ID_6179,GWAS_ID_6180,GWAS_ID_6181,GWAS_ID_6182,GWAS_ID_6183,GWAS_ID_6184,GWAS_ID_6185,GWAS_ID_6186,GWAS_ID_6187,GWAS_ID_6188,GWAS_ID_6189,GWAS_ID_6190,GWAS_ID_6191,GWAS_ID_6192,GWAS_ID_6193,GWAS_ID_6194,GWAS_ID_6195,GWAS_ID_6196,GWAS_ID_6197,GWAS_ID_6198,GWAS_ID_6199,GWAS_ID_6200,GWAS_ID_6201,GWAS_ID_6202,GWAS_ID_6203,GWAS_ID_6204,GWAS_ID_6205,GWAS_ID_6206,GWAS_ID_6207,GWAS_ID_6208,GWAS_ID_6209,GWAS_ID_6210,GWAS_ID_6211,GWAS_ID_6212,GWAS_ID_6213,GWAS_ID_6214,GWAS_ID_6215,GWAS_ID_6216,GWAS_ID_6217,GWAS_ID_6218,GWAS_ID_6219,GWAS_ID_6220,GWAS_ID_6221,GWAS_ID_6222,GWAS_ID_6223,GWAS_ID_6224,GWAS_ID_6225,GWAS_ID_6226,GWAS_ID_6227,GWAS_ID_6228,GWAS_ID_6229,GWAS_ID_6230,GWAS_ID_6231,GWAS_ID_6232,GWAS_ID_6233,GWAS_ID_6234,GWAS_ID_6235,GWAS_ID_6236,GWAS_ID_6237,GWAS_ID_6238,GWAS_ID_6239,GWAS_ID_6240,GWAS_ID_6241,GWAS_ID_6242,GWAS_ID_6243,GWAS_ID_6244,GWAS_ID_6245,GWAS_ID_6246,GWAS_ID_6247,GWAS_ID_6248,GWAS_ID_6249,GWAS_ID_6250,GWAS_ID_6251,GWAS_ID_6252,GWAS_ID_6253,GWAS_ID_6254,GWAS_ID_6255,GWAS_ID_6256,GWAS_ID_6257,GWAS_ID_6258,GWAS_ID_6259,GWAS_ID_6260,GWAS_ID_6261,GWAS_ID_6262,GWAS_ID_6263,GWAS_ID_6264,GWAS_ID_6265,GWAS_ID_6266,GWAS_ID_6267,GWAS_ID_6268,GWAS_ID_6269,GWAS_ID_6270,GWAS_ID_6271,GWAS_ID_6272,GWAS_ID_6273,GWAS_ID_6274,GWAS_ID_6275,GWAS_ID_6276,GWAS_ID_6277,GWAS_ID_6278,GWAS_ID_6279,GWAS_ID_6280,GWAS_ID_6281,GWAS_ID_6282,GWAS_ID_6283,GWAS_ID_6284,GWAS_ID_6285,GWAS_ID_6286,GWAS_ID_6287,GWAS_ID_6288,GWAS_ID_6289,GWAS_ID_6290,GWAS_ID_6291,GWAS_ID_6292,GWAS_ID_6293,GWAS_ID_6294,GWAS_ID_6295,GWAS_ID_6296,GWAS_ID_6297,GWAS_ID_6298,GWAS_ID_6299,GWAS_ID_6300,GWAS_ID_6301,GWAS_ID_6302,GWAS_ID_6303,GWAS_ID_6304,GWAS_ID_6305,GWAS_ID_6306,GWAS_ID_6307,GWAS_ID_6308,GWAS_ID_6309,GWAS_ID_6310,GWAS_ID_6311,GWAS_ID_6312,GWAS_ID_6313,GWAS_ID_6314,GWAS_ID_6315,GWAS_ID_6316,GWAS_ID_6317,GWAS_ID_6318,GWAS_ID_6319,GWAS_ID_6320,GWAS_ID_6321,GWAS_ID_6322,GWAS_ID_6323,GWAS_ID_6324,GWAS_ID_6325,GWAS_ID_6326,GWAS_ID_6327 RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_293925,RMVar_hsa_circ_183261,RMVar_hsa_circ_68200,RMVar_hsa_circ_183260 49977 RMVar_ID_49977 Human_SNP_ID_621724343 A-to-I Human chr17 + 30781514 30781514 30781514 TTGCCCAGGCTGGACTGTAATCATGTGATCTCAGCTCACTGTAACCTCTACCTCCCGGAGGGTTC TTGCCCAGGCTGGACTGTAATCATGTGATCTCTGCTCACTGTAACCTCTACCTCCCGGAGGGTTC A T SUZ12P1 Ensembl:ENSG00000264538 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1035563315 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2500805,Human_RBP_ID_12956587,Human_RBP_ID_17380295 RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_293925,RMVar_hsa_circ_183261,RMVar_hsa_circ_68200,RMVar_hsa_circ_183260 49978 RMVar_ID_49978 Human_SNP_ID_621724913 A-to-I Human chr17 - 30782969 30782962 30782969 TAAAATATTTATTTGAAGGACTTTAATATGTAAAAATAATTGTCTTCTATGCCACCCTACAGATT TAAAATATTTATTTGAAGGACTTTAATATGTA_______TTGTCTTCTATGCCACCCTACAGATT ATTATTTT A CRLF3 Ensembl:ENSG00000176390 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1444791202 Functional Loss DEL dbSNP153 33..39 33 - - - Human_RBP_ID_1530966,Human_RBP_ID_6579127,Human_RBP_ID_18290786,Human_RBP_ID_21890556,Human_RBP_ID_27663537 Human_miRNA_ID_689374 49979 RMVar_ID_49979 Human_SNP_ID_621724915 A-to-I Human chr17 - 30782970 30782970 30782970 GTAAAATATTTATTTGAAGGACTTTAATATGTAAAAATAATTGTCTTCTATGCCACCCTACAGAT GTAAAATATTTATTTGAAGGACTTTAATATGTGAAAATAATTGTCTTCTATGCCACCCTACAGAT T C CRLF3 Ensembl:ENSG00000176390 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs185459667 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1530966,Human_RBP_ID_6579127,Human_RBP_ID_18290786,Human_RBP_ID_21890556,Human_RBP_ID_23719769,Human_RBP_ID_27663537 Human_miRNA_ID_689374 49980 RMVar_ID_49980 Human_SNP_ID_621725121 A-to-I Human chr17 + 30783474 30783474 30783474 CCCTGTCTCTACTAAAAATACAAAAATTAGCCAGGTGTGGTGGCCGACGCCTGTAATCCCAGCTA CCCTGTCTCTACTAAAAATACAAAAATTAGCCGGGTGTGGTGGCCGACGCCTGTAATCCCAGCTA A G SUZ12P1 Ensembl:ENSG00000264538 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1004536108 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2500832 RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_293925,RMVar_hsa_circ_183261,RMVar_hsa_circ_68200,RMVar_hsa_circ_183260 49981 RMVar_ID_49981 Human_SNP_ID_621725729 A-to-I Human chr17 + 30784889 30784889 30784889 TAAGCAGTTCTCCTGCCTGAGCCTCTCGGATTACAGGTATGTACCACCACGCCCAGCTAATTTTT TAAGCAGTTCTCCTGCCTGAGCCTCTCGGATTGCAGGTATGTACCACCACGCCCAGCTAATTTTT A G SUZ12P1 Ensembl:ENSG00000264538 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1279614956 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5188026,Human_RBP_ID_8254306,Human_RBP_ID_19082052 Human_Splice_Rec_1800759 RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_293925,RMVar_hsa_circ_183261,RMVar_hsa_circ_68200,RMVar_hsa_circ_183260 49982 RMVar_ID_49982 Human_SNP_ID_621725950 A-to-I Human chr17 + 30785349 30785349 30785349 TGCCCGCCTTGGCCTCCCAAAGTGCTGGGATTAGAGGCGTGATCCACCGCGCCCGGCCTCTGGCT TGCCCGCCTTGGCCTCCCAAAGTGCTGGGATTGGAGGCGTGATCCACCGCGCCCGGCCTCTGGCT A G SUZ12P1 Ensembl:ENSG00000264538 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs755212570 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23168326 RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_68200 49983 RMVar_ID_49983 Human_SNP_ID_621726825 A-to-I Human chr17 + 30787810 30787810 30787810 TCACCTGAGGTCAGGAGTTCCAAGACCACCCTAGGCAACATGGTGAAACCCCGTATCTACAAAAA TCACCTGAGGTCAGGAGTTCCAAGACCACCCTGGGCAACATGGTGAAACCCCGTATCTACAAAAA A G SUZ12P1 Ensembl:ENSG00000264538 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1370595194 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247 49984 RMVar_ID_49984 Human_SNP_ID_621726838 A-to-I Human chr17 + 30787839 30787839 30787839 CCTAGGCAACATGGTGAAACCCCGTATCTACAAAAAATACAAAAATTAGCTGGGTGTGGTAGTGG CCTAGGCAACATGGTGAAACCCCGTATCTACAGAAAATACAAAAATTAGCTGGGTGTGGTAGTGG A G SUZ12P1 Ensembl:ENSG00000264538 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1028987368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12956795 RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247 49985 RMVar_ID_49985 Human_SNP_ID_621726850 A-to-I Human chr17 + 30787867 30787867 30787867 TACAAAAAATACAAAAATTAGCTGGGTGTGGTAGTGGCTCCTGTAATCCTAGCTACTCAGGAGGC TACAAAAAATACAAAAATTAGCTGGGTGTGGTCGTGGCTCCTGTAATCCTAGCTACTCAGGAGGC A C SUZ12P1 Ensembl:ENSG00000264538 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs980076305 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17565844 RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247 49986 RMVar_ID_49986 Human_SNP_ID_621726865 A-to-I Human chr17 + 30787915 30787915 30787915 CTAGCTACTCAGGAGGCTGAGGTGAGAGGGTCACTTGAACCTGTGAGATGGCGATTGCAGTGAGC CTAGCTACTCAGGAGGCTGAGGTGAGAGGGTCGCTTGAACCTGTGAGATGGCGATTGCAGTGAGC A G SUZ12P1 Ensembl:ENSG00000264538 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1445697332 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17380318,Human_RBP_ID_17565844,Human_RBP_ID_18514470 RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247 49987 RMVar_ID_49987 Human_SNP_ID_621728021 A-to-I Human chr17 - 30790745 30790745 30790745 GGGTGTGGTGAGGTGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAAGCAGGAGAATCACTGGAA GGGTGTGGTGAGGTGCGCCTGTAGTCCCAGCTGCTCGGGAGGCTGAAGCAGGAGAATCACTGGAA T C CRLF3 Ensembl:ENSG00000176390 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1344562224 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183266,RMVar_hsa_circ_295674,RMVar_hsa_circ_321585,RMVar_hsa_circ_356964,RMVar_hsa_circ_296154,RMVar_hsa_circ_294386,RMVar_hsa_circ_183264,RMVar_hsa_circ_183265,RMVar_hsa_circ_183263 49988 RMVar_ID_49988 Human_SNP_ID_621728601 A-to-I Human chr17 - 30792127 30792127 30792127 AAGTCAATCTTAGGCTGGGCATAGTGGTTCACACCTGTAACCCCAGCACTTTGGTAGGCCGAGGC AAGTCAATCTTAGGCTGGGCATAGTGGTTCACGCCTGTAACCCCAGCACTTTGGTAGGCCGAGGC T C CRLF3 Ensembl:ENSG00000176390 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs895196660 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25266986 RMVar_hsa_circ_183266,RMVar_hsa_circ_295674,RMVar_hsa_circ_321585,RMVar_hsa_circ_356964,RMVar_hsa_circ_296154,RMVar_hsa_circ_294386,RMVar_hsa_circ_183264,RMVar_hsa_circ_183265,RMVar_hsa_circ_183263 49989 RMVar_ID_49989 Human_SNP_ID_621729022 A-to-I Human chr17 - 30793123 30793123 30793123 TTATTTAGTTAGTTTTTTTGAGACAAGGTCTCACTCTGTCGCCCAGGCTGGTGTGTGGTGGTGCA TTATTTAGTTAGTTTTTTTGAGACAAGGTCTCGCTCTGTCGCCCAGGCTGGTGTGTGGTGGTGCA T C CRLF3 Ensembl:ENSG00000176390 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs376223751 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12956901 RMVar_hsa_circ_106638,RMVar_hsa_circ_183266,RMVar_hsa_circ_321585,RMVar_hsa_circ_356964,RMVar_hsa_circ_296154,RMVar_hsa_circ_294386,RMVar_hsa_circ_183264,RMVar_hsa_circ_183265,RMVar_hsa_circ_275967,RMVar_hsa_circ_284604,RMVar_hsa_circ_269047,RMVar_hsa_circ_183268,RMVar_hsa_circ_183269 49990 RMVar_ID_49990 Human_SNP_ID_621729024 A-to-I Human chr17 - 30793130 30793129 30793131 TTGAATGTTATTTAGTTAGTTTTTTTGAGACAAGGTCTCACTCTGTCGCCCAGGCTGGTGTGTGG TTGAATGTTATTTAGTTAGTTTTTTTGAGACGGAGTCTCACTCTGTCGCCCAGGCTGGTGTGTGG CTT TCC CRLF3 Ensembl:ENSG00000176390 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs386796437 Functional Loss MNV dbSNP153 32..34 33 - - - Human_RBP_ID_12956901 RMVar_hsa_circ_106638,RMVar_hsa_circ_183266,RMVar_hsa_circ_321585,RMVar_hsa_circ_356964,RMVar_hsa_circ_296154,RMVar_hsa_circ_294386,RMVar_hsa_circ_183264,RMVar_hsa_circ_183265,RMVar_hsa_circ_275967,RMVar_hsa_circ_284604,RMVar_hsa_circ_269047,RMVar_hsa_circ_183268,RMVar_hsa_circ_183269 49991 RMVar_ID_49991 Human_SNP_ID_621729026 A-to-I Human chr17 - 30793130 30793130 30793130 TTGAATGTTATTTAGTTAGTTTTTTTGAGACAAGGTCTCACTCTGTCGCCCAGGCTGGTGTGTGG TTGAATGTTATTTAGTTAGTTTTTTTGAGACAGGGTCTCACTCTGTCGCCCAGGCTGGTGTGTGG T C CRLF3 Ensembl:ENSG00000176390 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1334155035 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12956901 RMVar_hsa_circ_106638,RMVar_hsa_circ_183266,RMVar_hsa_circ_321585,RMVar_hsa_circ_356964,RMVar_hsa_circ_296154,RMVar_hsa_circ_294386,RMVar_hsa_circ_183264,RMVar_hsa_circ_183265,RMVar_hsa_circ_275967,RMVar_hsa_circ_284604,RMVar_hsa_circ_269047,RMVar_hsa_circ_183268,RMVar_hsa_circ_183269 49992 RMVar_ID_49992 Human_SNP_ID_621729288 A-to-I Human chr17 + 30793860 30793860 30793860 CACATCATTATCTCCCTTCTTTTTTTTTTGAGAAAGGGTCTCACTTTGTCACCCAGGCTGTAGTG CACATCATTATCTCCCTTCTTTTTTTTTTGAGGAAGGGTCTCACTTTGTCACCCAGGCTGTAGTG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs544256090 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_183270 49993 RMVar_ID_49993 Human_SNP_ID_621729301 A-to-I Human chr17 + 30793894 30793894 30793894 AGGGTCTCACTTTGTCACCCAGGCTGTAGTGCAGTGGCGTGATCTCGGCTTATTGCAGCCTCCAC AGGGTCTCACTTTGTCACCCAGGCTGTAGTGCCGTGGCGTGATCTCGGCTTATTGCAGCCTCCAC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900341222 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_183270 49994 RMVar_ID_49994 Human_SNP_ID_621729302 A-to-I Human chr17 + 30793894 30793894 30793894 AGGGTCTCACTTTGTCACCCAGGCTGTAGTGCAGTGGCGTGATCTCGGCTTATTGCAGCCTCCAC AGGGTCTCACTTTGTCACCCAGGCTGTAGTGCGGTGGCGTGATCTCGGCTTATTGCAGCCTCCAC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900341222 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_183270 49995 RMVar_ID_49995 Human_SNP_ID_621729373 A-to-I Human chr17 + 30794086 30794086 30794086 TAACTCCTGAGCTCAAGCAATCTTCTCGTCTCAGCCTCTCAAAGTGCTAGGACTATAGGCGTGAG TAACTCCTGAGCTCAAGCAATCTTCTCGTCTCGGCCTCTCAAAGTGCTAGGACTATAGGCGTGAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs114913263 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_183270 49996 RMVar_ID_49996 Human_SNP_ID_621729552 A-to-I Human chr17 + 30794684 30794684 30794684 AGCTGGCTGTGGAAGCACATGCCTGAAGTCCCAATTACTTGGGGGCTGAGGCGGGAGGATCACTT AGCTGGCTGTGGAAGCACATGCCTGAAGTCCCCATTACTTGGGGGCTGAGGCGGGAGGATCACTT A C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1196689474 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_183270 49997 RMVar_ID_49997 Human_SNP_ID_621729578 A-to-I Human chr17 + 30794776 30794775 30794777 TGATTGTGCCACTGTACTCCAGCCTGGGTGACAGAGTGAGACCCTGTCTCAAAAACAAACAAATA TGATTGTGCCACTGTACTCCAGCCTGGGTGAC__AGTGAGACCCTGTCTCAAAAACAAACAAATA CAG C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs367869437 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_183270 49998 RMVar_ID_49998 Human_SNP_ID_621729579 A-to-I Human chr17 + 30794776 30794776 30794776 TGATTGTGCCACTGTACTCCAGCCTGGGTGACAGAGTGAGACCCTGTCTCAAAAACAAACAAATA TGATTGTGCCACTGTACTCCAGCCTGGGTGACGGAGTGAGACCCTGTCTCAAAAACAAACAAATA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1129356 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_183270 49999 RMVar_ID_49999 Human_SNP_ID_621729945 A-to-I Human chr17 + 30795813 30795813 30795813 CAAAAATTAGGCAGGTGTGATGGCAGGTGCCTATAATCCCAGCTACTCAGGAGGCCGAAGCAGGA CAAAAATTAGGCAGGTGTGATGGCAGGTGCCTTTAATCCCAGCTACTCAGGAGGCCGAAGCAGGA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs897818835 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247 50000 RMVar_ID_50000 Human_SNP_ID_621729954 A-to-I Human chr17 + 30795838 30795838 30795838 GGTGCCTATAATCCCAGCTACTCAGGAGGCCGAAGCAGGAGAATGGCTTGAACCCGGGGGAAGCG GGTGCCTATAATCCCAGCTACTCAGGAGGCCGGAGCAGGAGAATGGCTTGAACCCGGGGGAAGCG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1416401574 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23308142 RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247 50001 RMVar_ID_50001 Human_SNP_ID_621730845 A-to-I Human chr17 - 30798723 30798723 30798723 GCGATTCTAGTGCCTCAGCCTCCCTAGTAGCTAGAACTACAGGAGCGTGCCACTATGCCCAGCTA GCGATTCTAGTGCCTCAGCCTCCCTAGTAGCTGGAACTACAGGAGCGTGCCACTATGCCCAGCTA T C CRLF3 Ensembl:ENSG00000176390 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1272580261 Functional Loss SNV dbSNP153 33..33 33 - - - 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 50002 RMVar_ID_50002 Human_SNP_ID_621732403 A-to-I Human chr17 - 30805100 30805100 30805100 TGGATCCCTGCAACCTCCATCTCCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCGCAAGTAGCT TGGATCCCTGCAACCTCCATCTCCCAGGTTCAGGCAATTCTCCTGCCTCAGCCTCGCAAGTAGCT T C CRLF3 Ensembl:ENSG00000176390 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1457888757 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106638,RMVar_hsa_circ_183269 50003 RMVar_ID_50003 Human_SNP_ID_621732419 A-to-I Human chr17 - 30805168 30805158 30805168 TTATTTATTTCTCTTTTTTGAAATGGCGTCTCACTCTGTTGCCCAGCTGGAGTGCAGTGGCGCAA TTATTTATTTCTCTTTTTTGAAATGGCGTCTC__________CCAGCTGGAGTGCAGTGGCGCAA GGCAACAGAGT G CRLF3 Ensembl:ENSG00000176390 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1437111683 Functional Loss DEL dbSNP153 33..42 33 - - - RMVar_hsa_circ_106638,RMVar_hsa_circ_183269 50004 RMVar_ID_50004 Human_SNP_ID_621733601 A-to-I Human chr17 - 30809743 30809743 30809743 GGGAGGCTAAGGTGGGAGAATCACCTGAGCCCAGGAGTTCGAGGCCGCAGTGAGTTGTGATTGTA GGGAGGCTAAGGTGGGAGAATCACCTGAGCCCGGGAGTTCGAGGCCGCAGTGAGTTGTGATTGTA T C CRLF3 Ensembl:ENSG00000176390 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350744445 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106638,RMVar_hsa_circ_183269 50005 RMVar_ID_50005 Human_SNP_ID_621733614 A-to-I Human chr17 - 30809805 30809802 30809805 CTCGACAAAAAATACAAAATATAGCTGGGTGTAGTGACACATGCCTGTGGTCCCAGCTACCTGGG CTCGACAAAAAATACAAAATATAGCTGGGTGT___GACACATGCCTGTGGTCCCAGCTACCTGGG CACT C CRLF3 Ensembl:ENSG00000176390 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1490778540 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_106638,RMVar_hsa_circ_183269 50006 RMVar_ID_50006 Human_SNP_ID_621733639 A-to-I Human chr17 - 30809930 30809930 30809930 ATAGTGTTCTATGGCCGAGCGCGGTGGCTCACACTTGTAATCTCAGCACTTTGAGAGGCCGAGGC ATAGTGTTCTATGGCCGAGCGCGGTGGCTCACGCTTGTAATCTCAGCACTTTGAGAGGCCGAGGC T C CRLF3 Ensembl:ENSG00000176390 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs897234891 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106638,RMVar_hsa_circ_183269 50007 RMVar_ID_50007 Human_SNP_ID_621735399 A-to-I Human chr17 - 30816690 30816690 30816690 GCCCAGAAGTTTGAGACCAGTCTGGGCAATATAGGGAGACCCCCATCTCCACAAAGAAATTAAAA GCCCAGAAGTTTGAGACCAGTCTGGGCAATATGGGGAGACCCCCATCTCCACAAAGAAATTAAAA T C CRLF3 Ensembl:ENSG00000176390 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs185044630 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_106638,RMVar_hsa_circ_183269 50008 RMVar_ID_50008 Human_SNP_ID_621744019 A-to-I Human chr17 + 30850018 30850018 30850018 AAACAACTAGCCAGGCATGGTGGTGTATGCCTATAGGCCCAGCTACTTGGGAGTCTGAGACAGGA AAACAACTAGCCAGGCATGGTGGTGTATGCCTTTAGGCCCAGCTACTTGGGAGTCTGAGACAGGA A T ATAD5 Ensembl:ENSG00000176208 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1356655840 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2087002,Human_miRNA_ID_2087003 RMVar_hsa_circ_5712,RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_88089,RMVar_hsa_circ_62115,RMVar_hsa_circ_356617,RMVar_hsa_circ_183276,RMVar_hsa_circ_73387,RMVar_hsa_circ_3359,RMVar_hsa_circ_282773,RMVar_hsa_circ_332900,RMVar_hsa_circ_288954,RMVar_hsa_circ_126547,RMVar_hsa_circ_5542,RMVar_hsa_circ_183280,RMVar_hsa_circ_183282,RMVar_hsa_circ_183283,RMVar_hsa_circ_183281,RMVar_hsa_circ_76606,RMVar_hsa_circ_368594,RMVar_hsa_circ_183285,RMVar_hsa_circ_11017 50009 RMVar_ID_50009 Human_SNP_ID_621744020 A-to-I Human chr17 + 30850020 30850020 30850020 ACAACTAGCCAGGCATGGTGGTGTATGCCTATAGGCCCAGCTACTTGGGAGTCTGAGACAGGAGG ACAACTAGCCAGGCATGGTGGTGTATGCCTATCGGCCCAGCTACTTGGGAGTCTGAGACAGGAGG A C ATAD5 Ensembl:ENSG00000176208 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs969025710 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2087002,Human_miRNA_ID_2087003 RMVar_hsa_circ_5712,RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_88089,RMVar_hsa_circ_62115,RMVar_hsa_circ_356617,RMVar_hsa_circ_183276,RMVar_hsa_circ_73387,RMVar_hsa_circ_3359,RMVar_hsa_circ_282773,RMVar_hsa_circ_332900,RMVar_hsa_circ_288954,RMVar_hsa_circ_126547,RMVar_hsa_circ_5542,RMVar_hsa_circ_183280,RMVar_hsa_circ_183282,RMVar_hsa_circ_183283,RMVar_hsa_circ_183281,RMVar_hsa_circ_76606,RMVar_hsa_circ_368594,RMVar_hsa_circ_183285,RMVar_hsa_circ_11017 50010 RMVar_ID_50010 Human_SNP_ID_621744033 A-to-I Human chr17 + 30850092 30850092 30850092 GAGCCTGGGAGGTCATGGCTGCAGTGAGCTGTAATCATGCCACTGCACTCCAGCTTGGGTAACAG GAGCCTGGGAGGTCATGGCTGCAGTGAGCTGTGATCATGCCACTGCACTCCAGCTTGGGTAACAG A G ATAD5 Ensembl:ENSG00000176208 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs953112440 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12957822 RMVar_hsa_circ_5712,RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_88089,RMVar_hsa_circ_62115,RMVar_hsa_circ_356617,RMVar_hsa_circ_183276,RMVar_hsa_circ_73387,RMVar_hsa_circ_3359,RMVar_hsa_circ_282773,RMVar_hsa_circ_332900,RMVar_hsa_circ_288954,RMVar_hsa_circ_126547,RMVar_hsa_circ_5542,RMVar_hsa_circ_183280,RMVar_hsa_circ_183282,RMVar_hsa_circ_183283,RMVar_hsa_circ_183281,RMVar_hsa_circ_76606,RMVar_hsa_circ_368594,RMVar_hsa_circ_183285,RMVar_hsa_circ_11017 50011 RMVar_ID_50011 Human_SNP_ID_621744125 A-to-I Human chr17 + 30850473 30850473 30850473 GCCTCAACCTCCTGGGTTCAAGTGATCCTGCCATCTCAGCCCCTCAAATAGCTGGAACCACAGAT GCCTCAACCTCCTGGGTTCAAGTGATCCTGCCGTCTCAGCCCCTCAAATAGCTGGAACCACAGAT A G ATAD5 Ensembl:ENSG00000176208 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs952261608 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5712,RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_88089,RMVar_hsa_circ_62115,RMVar_hsa_circ_356617,RMVar_hsa_circ_183276,RMVar_hsa_circ_73387,RMVar_hsa_circ_3359,RMVar_hsa_circ_282773,RMVar_hsa_circ_332900,RMVar_hsa_circ_288954,RMVar_hsa_circ_126547,RMVar_hsa_circ_5542,RMVar_hsa_circ_183280,RMVar_hsa_circ_183282,RMVar_hsa_circ_183283,RMVar_hsa_circ_183281,RMVar_hsa_circ_76606,RMVar_hsa_circ_368594,RMVar_hsa_circ_183285,RMVar_hsa_circ_11017 50012 RMVar_ID_50012 Human_SNP_ID_621744126 A-to-I Human chr17 + 30850473 30850473 30850473 GCCTCAACCTCCTGGGTTCAAGTGATCCTGCCATCTCAGCCCCTCAAATAGCTGGAACCACAGAT GCCTCAACCTCCTGGGTTCAAGTGATCCTGCCTTCTCAGCCCCTCAAATAGCTGGAACCACAGAT A T ATAD5 Ensembl:ENSG00000176208 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs952261608 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5712,RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_88089,RMVar_hsa_circ_62115,RMVar_hsa_circ_356617,RMVar_hsa_circ_183276,RMVar_hsa_circ_73387,RMVar_hsa_circ_3359,RMVar_hsa_circ_282773,RMVar_hsa_circ_332900,RMVar_hsa_circ_288954,RMVar_hsa_circ_126547,RMVar_hsa_circ_5542,RMVar_hsa_circ_183280,RMVar_hsa_circ_183282,RMVar_hsa_circ_183283,RMVar_hsa_circ_183281,RMVar_hsa_circ_76606,RMVar_hsa_circ_368594,RMVar_hsa_circ_183285,RMVar_hsa_circ_11017 50013 RMVar_ID_50013 Human_SNP_ID_621744628 A-to-I Human chr17 + 30851535 30851535 30851535 AAAAAAAAAAATCCTAAGGGTAGGCCAGGCATAGTGGCTCACACCTGTAATCCCAACACTCTGGG AAAAAAAAAAATCCTAAGGGTAGGCCAGGCATGGTGGCTCACACCTGTAATCCCAACACTCTGGG A G ATAD5 Ensembl:ENSG00000176208 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs888221916 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5712,RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_88089,RMVar_hsa_circ_62115,RMVar_hsa_circ_356617,RMVar_hsa_circ_183276,RMVar_hsa_circ_73387,RMVar_hsa_circ_3359,RMVar_hsa_circ_282773,RMVar_hsa_circ_332900,RMVar_hsa_circ_288954,RMVar_hsa_circ_126547,RMVar_hsa_circ_5542,RMVar_hsa_circ_183280,RMVar_hsa_circ_183282,RMVar_hsa_circ_183283,RMVar_hsa_circ_183281,RMVar_hsa_circ_76606,RMVar_hsa_circ_368594,RMVar_hsa_circ_183285,RMVar_hsa_circ_11017 50014 RMVar_ID_50014 Human_SNP_ID_621744667 A-to-I Human chr17 + 30851722 30851722 30851722 ATCGTGCCTTAGCCTCCCAAGTAGCTGGGATTACAGGTATGCACCACCACACCTGGCTAATTTTT ATCGTGCCTTAGCCTCCCAAGTAGCTGGGATTGCAGGTATGCACCACCACACCTGGCTAATTTTT A G ATAD5 Ensembl:ENSG00000176208 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1184422780 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5712,RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_88089,RMVar_hsa_circ_62115,RMVar_hsa_circ_356617,RMVar_hsa_circ_183276,RMVar_hsa_circ_73387,RMVar_hsa_circ_3359,RMVar_hsa_circ_282773,RMVar_hsa_circ_332900,RMVar_hsa_circ_288954,RMVar_hsa_circ_126547,RMVar_hsa_circ_5542,RMVar_hsa_circ_183280,RMVar_hsa_circ_183282,RMVar_hsa_circ_183283,RMVar_hsa_circ_183281,RMVar_hsa_circ_76606,RMVar_hsa_circ_368594,RMVar_hsa_circ_183285,RMVar_hsa_circ_11017 50015 RMVar_ID_50015 Human_SNP_ID_621747274 A-to-I Human chr17 + 30862933 30862933 30862933 ATACCTGGGGCCAGGCACCATGGCTCATCCCTATAATCCCAGCACTTTGAGAGGCCGAGGTGGGA ATACCTGGGGCCAGGCACCATGGCTCATCCCTGTAATCCCAGCACTTTGAGAGGCCGAGGTGGGA A G ATAD5 Ensembl:ENSG00000176208 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs552212859 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17565846,Human_RBP_ID_25267296 RMVar_hsa_circ_5712,RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_3359,RMVar_hsa_circ_332900,RMVar_hsa_circ_126547,RMVar_hsa_circ_183280,RMVar_hsa_circ_183282,RMVar_hsa_circ_183281,RMVar_hsa_circ_76606,RMVar_hsa_circ_368594,RMVar_hsa_circ_48247,RMVar_hsa_circ_1660,RMVar_hsa_circ_56710,RMVar_hsa_circ_183285,RMVar_hsa_circ_272678,RMVar_hsa_circ_47714,RMVar_hsa_circ_183289,RMVar_hsa_circ_297690,RMVar_hsa_circ_309881,RMVar_hsa_circ_183286,RMVar_hsa_circ_367138,RMVar_hsa_circ_302338,RMVar_hsa_circ_272952,RMVar_hsa_circ_183287,RMVar_hsa_circ_183288,RMVar_hsa_circ_312372,RMVar_hsa_circ_356291,RMVar_hsa_circ_363725,RMVar_hsa_circ_332740,RMVar_hsa_circ_58048,RMVar_hsa_circ_183290,RMVar_hsa_circ_183291,RMVar_hsa_circ_363572 50016 RMVar_ID_50016 Human_SNP_ID_621747306 A-to-I Human chr17 + 30863077 30863077 30863077 AAAATTGGCTAGGCATGGTGGCACATGCCTGTAGTCTCAGCTCCACAGGAGGCTGATGTGAGAGG AAAATTGGCTAGGCATGGTGGCACATGCCTGTGGTCTCAGCTCCACAGGAGGCTGATGTGAGAGG A G ATAD5 Ensembl:ENSG00000176208 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs989934590 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17566422 RMVar_hsa_circ_5712,RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_3359,RMVar_hsa_circ_332900,RMVar_hsa_circ_126547,RMVar_hsa_circ_183280,RMVar_hsa_circ_183282,RMVar_hsa_circ_183281,RMVar_hsa_circ_76606,RMVar_hsa_circ_368594,RMVar_hsa_circ_48247,RMVar_hsa_circ_1660,RMVar_hsa_circ_56710,RMVar_hsa_circ_183285,RMVar_hsa_circ_272678,RMVar_hsa_circ_47714,RMVar_hsa_circ_183289,RMVar_hsa_circ_297690,RMVar_hsa_circ_309881,RMVar_hsa_circ_183286,RMVar_hsa_circ_367138,RMVar_hsa_circ_302338,RMVar_hsa_circ_272952,RMVar_hsa_circ_183287,RMVar_hsa_circ_183288,RMVar_hsa_circ_312372,RMVar_hsa_circ_356291,RMVar_hsa_circ_363725,RMVar_hsa_circ_332740,RMVar_hsa_circ_58048,RMVar_hsa_circ_183290,RMVar_hsa_circ_183291,RMVar_hsa_circ_363572 50017 RMVar_ID_50017 Human_SNP_ID_621747307 A-to-I Human chr17 + 30863077 30863077 30863077 AAAATTGGCTAGGCATGGTGGCACATGCCTGTAGTCTCAGCTCCACAGGAGGCTGATGTGAGAGG AAAATTGGCTAGGCATGGTGGCACATGCCTGTTGTCTCAGCTCCACAGGAGGCTGATGTGAGAGG A T ATAD5 Ensembl:ENSG00000176208 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs989934590 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17566422 RMVar_hsa_circ_5712,RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_3359,RMVar_hsa_circ_332900,RMVar_hsa_circ_126547,RMVar_hsa_circ_183280,RMVar_hsa_circ_183282,RMVar_hsa_circ_183281,RMVar_hsa_circ_76606,RMVar_hsa_circ_368594,RMVar_hsa_circ_48247,RMVar_hsa_circ_1660,RMVar_hsa_circ_56710,RMVar_hsa_circ_183285,RMVar_hsa_circ_272678,RMVar_hsa_circ_47714,RMVar_hsa_circ_183289,RMVar_hsa_circ_297690,RMVar_hsa_circ_309881,RMVar_hsa_circ_183286,RMVar_hsa_circ_367138,RMVar_hsa_circ_302338,RMVar_hsa_circ_272952,RMVar_hsa_circ_183287,RMVar_hsa_circ_183288,RMVar_hsa_circ_312372,RMVar_hsa_circ_356291,RMVar_hsa_circ_363725,RMVar_hsa_circ_332740,RMVar_hsa_circ_58048,RMVar_hsa_circ_183290,RMVar_hsa_circ_183291,RMVar_hsa_circ_363572 50018 RMVar_ID_50018 Human_SNP_ID_621748165 A-to-I Human chr17 + 30866291 30866291 30866291 ACGATCTTGGCTCACTACAGTCGCTGCCTCCCAGGTTCAACAGATTCTCCTGCCTCAGCCTCCTG ACGATCTTGGCTCACTACAGTCGCTGCCTCCCGGGTTCAACAGATTCTCCTGCCTCAGCCTCCTG A G ATAD5 Ensembl:ENSG00000176208 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1375871906 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5712,RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_3359,RMVar_hsa_circ_332900,RMVar_hsa_circ_126547,RMVar_hsa_circ_183280,RMVar_hsa_circ_183282,RMVar_hsa_circ_183281,RMVar_hsa_circ_76606,RMVar_hsa_circ_368594,RMVar_hsa_circ_48247,RMVar_hsa_circ_1660,RMVar_hsa_circ_56710,RMVar_hsa_circ_183285,RMVar_hsa_circ_272678,RMVar_hsa_circ_183289,RMVar_hsa_circ_309881,RMVar_hsa_circ_183286,RMVar_hsa_circ_367138,RMVar_hsa_circ_302338,RMVar_hsa_circ_272952,RMVar_hsa_circ_183288,RMVar_hsa_circ_312372,RMVar_hsa_circ_356291,RMVar_hsa_circ_363725,RMVar_hsa_circ_58048,RMVar_hsa_circ_26596,RMVar_hsa_circ_183291,RMVar_hsa_circ_271609,RMVar_hsa_circ_363572,RMVar_hsa_circ_183292 50019 RMVar_ID_50019 Human_SNP_ID_621748254 A-to-I Human chr17 + 30866704 30866704 30866704 GGGTGTGGTGATGCACGCCTGTAATCCTGGCTACTGGAGAGGCTGAGGCATGAGAATCGCCTGAA GGGTGTGGTGATGCACGCCTGTAATCCTGGCTGCTGGAGAGGCTGAGGCATGAGAATCGCCTGAA A G ATAD5 Ensembl:ENSG00000176208 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs919538324 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5712,RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_3359,RMVar_hsa_circ_332900,RMVar_hsa_circ_126547,RMVar_hsa_circ_183280,RMVar_hsa_circ_183282,RMVar_hsa_circ_183281,RMVar_hsa_circ_76606,RMVar_hsa_circ_368594,RMVar_hsa_circ_48247,RMVar_hsa_circ_1660,RMVar_hsa_circ_56710,RMVar_hsa_circ_183285,RMVar_hsa_circ_272678,RMVar_hsa_circ_183289,RMVar_hsa_circ_309881,RMVar_hsa_circ_183286,RMVar_hsa_circ_367138,RMVar_hsa_circ_302338,RMVar_hsa_circ_272952,RMVar_hsa_circ_183288,RMVar_hsa_circ_312372,RMVar_hsa_circ_356291,RMVar_hsa_circ_363725,RMVar_hsa_circ_58048,RMVar_hsa_circ_26596,RMVar_hsa_circ_183291,RMVar_hsa_circ_271609,RMVar_hsa_circ_363572,RMVar_hsa_circ_183292 50020 RMVar_ID_50020 Human_SNP_ID_621748266 A-to-I Human chr17 + 30866756 30866756 30866756 AGAATCGCCTGAACCCGGGAGGTGAGGATTGCAGCGAGCCGAGGTCGTGCCAGTGCACTCCAGCC AGAATCGCCTGAACCCGGGAGGTGAGGATTGCCGCGAGCCGAGGTCGTGCCAGTGCACTCCAGCC A C ATAD5 Ensembl:ENSG00000176208 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1362635190 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6579545 RMVar_hsa_circ_5712,RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_3359,RMVar_hsa_circ_332900,RMVar_hsa_circ_126547,RMVar_hsa_circ_183280,RMVar_hsa_circ_183282,RMVar_hsa_circ_183281,RMVar_hsa_circ_76606,RMVar_hsa_circ_368594,RMVar_hsa_circ_48247,RMVar_hsa_circ_1660,RMVar_hsa_circ_56710,RMVar_hsa_circ_183285,RMVar_hsa_circ_272678,RMVar_hsa_circ_183289,RMVar_hsa_circ_309881,RMVar_hsa_circ_183286,RMVar_hsa_circ_367138,RMVar_hsa_circ_302338,RMVar_hsa_circ_272952,RMVar_hsa_circ_183288,RMVar_hsa_circ_312372,RMVar_hsa_circ_356291,RMVar_hsa_circ_363725,RMVar_hsa_circ_58048,RMVar_hsa_circ_26596,RMVar_hsa_circ_183291,RMVar_hsa_circ_271609,RMVar_hsa_circ_363572,RMVar_hsa_circ_183292 50021 RMVar_ID_50021 Human_SNP_ID_621748388 A-to-I Human chr17 + 30867173 30867173 30867173 TGTAATCCCAGTGCTTTCGTAAGCTGAGGCAGAAGGACTGCTTGTGGCCAGGAGTTTGAGAGCAG TGTAATCCCAGTGCTTTCGTAAGCTGAGGCAGCAGGACTGCTTGTGGCCAGGAGTTTGAGAGCAG A C ATAD5 Ensembl:ENSG00000176208 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1430120151 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5712,RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_3359,RMVar_hsa_circ_332900,RMVar_hsa_circ_126547,RMVar_hsa_circ_183280,RMVar_hsa_circ_183282,RMVar_hsa_circ_183281,RMVar_hsa_circ_76606,RMVar_hsa_circ_368594,RMVar_hsa_circ_48247,RMVar_hsa_circ_1660,RMVar_hsa_circ_56710,RMVar_hsa_circ_183285,RMVar_hsa_circ_272678,RMVar_hsa_circ_183289,RMVar_hsa_circ_309881,RMVar_hsa_circ_183286,RMVar_hsa_circ_367138,RMVar_hsa_circ_302338,RMVar_hsa_circ_272952,RMVar_hsa_circ_183288,RMVar_hsa_circ_312372,RMVar_hsa_circ_356291,RMVar_hsa_circ_363725,RMVar_hsa_circ_58048,RMVar_hsa_circ_26596,RMVar_hsa_circ_183291,RMVar_hsa_circ_271609,RMVar_hsa_circ_363572,RMVar_hsa_circ_183292 50022 RMVar_ID_50022 Human_SNP_ID_621749632 A-to-I Human chr17 + 30872604 30872603 30872604 TTGAGACGGAGTCTCACACTGTTGCCTGGGCTAGAGTGCAGTGGTGCGATCTTGGTGCACTGCAA TTGAGACGGAGTCTCACACTGTTGCCTGGGCT_GAGTGCAGTGGTGCGATCTTGGTGCACTGCAA TA T ATAD5 Ensembl:ENSG00000176208 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1181485755 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_3359,RMVar_hsa_circ_183280,RMVar_hsa_circ_76606,RMVar_hsa_circ_48247,RMVar_hsa_circ_1660,RMVar_hsa_circ_56710,RMVar_hsa_circ_183285,RMVar_hsa_circ_183289,RMVar_hsa_circ_309881,RMVar_hsa_circ_367138,RMVar_hsa_circ_272952,RMVar_hsa_circ_356291,RMVar_hsa_circ_363725,RMVar_hsa_circ_58048,RMVar_hsa_circ_68945,RMVar_hsa_circ_345645,RMVar_hsa_circ_26596,RMVar_hsa_circ_354965,RMVar_hsa_circ_337711,RMVar_hsa_circ_67029,RMVar_hsa_circ_319105 50023 RMVar_ID_50023 Human_SNP_ID_621751302 A-to-I Human chr17 - 30879285 30879284 30879286 CCCACCACTGCCTAGTGCTGTGGTGCAGTCATAGCTCACTGCAGCCTCAAACTCCTGGGCTCAAG CCCACCACTGCCTAGTGCTGTGGTGCAGTCA__GCTCACTGCAGCCTCAAACTCCTGGGCTCAAG CTA C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1242188131 Functional Loss DEL dbSNP153 32..33 33 - - - 50024 RMVar_ID_50024 Human_SNP_ID_621751539 A-to-I Human chr17 + 30880147 30880147 30880147 AACATGGCAAAACCCTGTCTCTACACAAAAATACAAAAAATTAGCCAGGTGTGGTGGCACATGCC AACATGGCAAAACCCTGTCTCTACACAAAAATGCAAAAAATTAGCCAGGTGTGGTGGCACATGCC A G ATAD5 Ensembl:ENSG00000176208 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1362194270 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_183280,RMVar_hsa_circ_1660,RMVar_hsa_circ_183289,RMVar_hsa_circ_272952,RMVar_hsa_circ_363725,RMVar_hsa_circ_26596,RMVar_hsa_circ_337711,RMVar_hsa_circ_265847,RMVar_hsa_circ_319105,RMVar_hsa_circ_340219,RMVar_hsa_circ_40265 50025 RMVar_ID_50025 Human_SNP_ID_621751874 A-to-I Human chr17 + 30881541 30881541 30881541 GCCAGGCTGGCTTTGAACTCTTGACCTCAAGTAATCCACCCACCTTGGCCTCTTAAAGAGCTGGG GCCAGGCTGGCTTTGAACTCTTGACCTCAAGTCATCCACCCACCTTGGCCTCTTAAAGAGCTGGG A C ATAD5 Ensembl:ENSG00000176208 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1221817383 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_183280,RMVar_hsa_circ_1660,RMVar_hsa_circ_183289,RMVar_hsa_circ_272952,RMVar_hsa_circ_363725,RMVar_hsa_circ_26596,RMVar_hsa_circ_337711,RMVar_hsa_circ_265847,RMVar_hsa_circ_319105,RMVar_hsa_circ_340219,RMVar_hsa_circ_40265 50026 RMVar_ID_50026 Human_SNP_ID_621752099 A-to-I Human chr17 - 30882371 30882371 30882371 TTTGTAGAGACAGGATTTCGCCAATGTTGCCCAGGCTGGTCTTGAACTTCTGGGCTCAAGGGATC TTTGTAGAGACAGGATTTCGCCAATGTTGCCCCGGCTGGTCTTGAACTTCTGGGCTCAAGGGATC T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1375343723 Functional Loss SNV dbSNP153 33..33 33 - - - 50027 RMVar_ID_50027 Human_SNP_ID_621753422 A-to-I Human chr17 - 30887719 30887719 30887719 CTCAAACTCTTCGGGGATCATGTGATCCTCCTACCTCAGCCTCCCGGGTAGCCAGTATTACAGGC CTCAAACTCTTCGGGGATCATGTGATCCTCCTCCCTCAGCCTCCCGGGTAGCCAGTATTACAGGC T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1249667030 Functional Loss SNV dbSNP153 33..33 33 - - - 50028 RMVar_ID_50028 Human_SNP_ID_621754488 A-to-I Human chr17 + 30891959 30891959 30891959 GAACTCCTGAACTCAAGTGATCCACCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG GAACTCCTGAACTCAAGTGATCCACCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG A G ATAD5 Ensembl:ENSG00000176208 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1330104640 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247 50029 RMVar_ID_50029 Human_SNP_ID_621756121 A-to-I Human chr17 + 30898463 30898463 30898463 CTGCCACCCAGTTCAAGCGATTCTCCTGTCTCAGCCTCCTGAGTAGCTGGGGCTACAGGCATGCG CTGCCACCCAGTTCAAGCGATTCTCCTGTCTCGGCCTCCTGAGTAGCTGGGGCTACAGGCATGCG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978169347 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247 50030 RMVar_ID_50030 Human_SNP_ID_621756124 A-to-I Human chr17 - 30898470 30898470 30898470 GTGGTGGCGCATGCCTGTAGCCCCAGCTACTCAGGAGGCTGAGACAGGAGAATCGCTTGAACTGG GTGGTGGCGCATGCCTGTAGCCCCAGCTACTCGGGAGGCTGAGACAGGAGAATCGCTTGAACTGG T C TEFM Ensembl:ENSG00000172171 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1168668264 Functional Loss SNV dbSNP153 33..33 33 - - - 50031 RMVar_ID_50031 Human_SNP_ID_621756125 A-to-I Human chr17 - 30898478 30898478 30898478 AGCCGGGTGTGGTGGCGCATGCCTGTAGCCCCAGCTACTCAGGAGGCTGAGACAGGAGAATCGCT AGCCGGGTGTGGTGGCGCATGCCTGTAGCCCCGGCTACTCAGGAGGCTGAGACAGGAGAATCGCT T C TEFM Ensembl:ENSG00000172171 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs923982730 Functional Loss SNV dbSNP153 33..33 33 - - - 50032 RMVar_ID_50032 Human_SNP_ID_621771318 A-to-I Human chr17 + 30960946 30960946 30960946 TATTTTTAGTAGAGACAGGGTTTCATCATGTTAGCCAGGAGGGTCTCGATCTCCCAACCTCGTGA TATTTTTAGTAGAGACAGGGTTTCATCATGTTGGCCAGGAGGGTCTCGATCTCCCAACCTCGTGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs567624718 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247 50033 RMVar_ID_50033 Human_SNP_ID_621774560 A-to-I Human chr17 + 30972006 30972006 30972006 TAGAGACGGGGTTTCGACATGTTAGCCAGGCTAGTCTCAAACTCTTGACCACAGATGATCCGTCC TAGAGACGGGGTTTCGACATGTTAGCCAGGCTTGTCTCAAACTCTTGACCACAGATGATCCGTCC A T AC138207.4,RNF135 Ensembl:ENSG00000264456,Ensembl:ENSG00000181481 lincRNA,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886828097 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12958887 RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247 50034 RMVar_ID_50034 Human_SNP_ID_621775159 A-to-I Human chr17 + 30974057 30974057 30974057 GAAACCCCATCTCTAGAAAAATACAAAAAATTAGCTGGGCATGGTGGCATGTGCCTGTAGTCCCA GAAACCCCATCTCTAGAAAAATACAAAAAATTCGCTGGGCATGGTGGCATGTGCCTGTAGTCCCA A C RNF135 Ensembl:ENSG00000181481 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1003226439 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247 50035 RMVar_ID_50035 Human_SNP_ID_621775405 A-to-I Human chr17 + 30975087 30975087 30975087 GAAGCAGGAGGATTGCTTGAGCCCAGGAGTTCAAGACCAGCCTGGGCAGCATGGTGAGATCCAAT GAAGCAGGAGGATTGCTTGAGCCCAGGAGTTCCAGACCAGCCTGGGCAGCATGGTGAGATCCAAT A C RNF135 Ensembl:ENSG00000181481 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1361756114 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247 50036 RMVar_ID_50036 Human_SNP_ID_621775447 A-to-I Human chr17 + 30975248 30975248 30975248 GCGAGACTGAGGTACGAAGAACACTTGAATCCAGGAGGTTGAGGCTGCAGTGAGCTGTTTTCATG GCGAGACTGAGGTACGAAGAACACTTGAATCCGGGAGGTTGAGGCTGCAGTGAGCTGTTTTCATG A G RNF135 Ensembl:ENSG00000181481 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs540491977 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247 50037 RMVar_ID_50037 Human_SNP_ID_621805804 A-to-I Human chr17 + 31102561 31102561 31102561 GGCCTTGAATTCAAGACCAGGCTGTGCAACATAGTGAGATGCTGTCTCTAAAAAAAATTAGTTGG GGCCTTGAATTCAAGACCAGGCTGTGCAACATGGTGAGATGCTGTCTCTAAAAAAAATTAGTTGG A G NF1 Ensembl:ENSG00000196712 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1044220079 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183307,RMVar_hsa_circ_95146 50038 RMVar_ID_50038 Human_SNP_ID_621809016 A-to-I Human chr17 + 31116945 31116945 31116945 GTGATTCACCTTCCTCGGCCTCCCAAAGTGCTAGGGTTACAGGCATGAGCCACTGTGCCTGGCTC GTGATTCACCTTCCTCGGCCTCCCAAAGTGCTGGGGTTACAGGCATGAGCCACTGTGCCTGGCTC A G NF1 Ensembl:ENSG00000196712 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1274687231 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183307,RMVar_hsa_circ_95146 50039 RMVar_ID_50039 Human_SNP_ID_621812742 A-to-I Human chr17 + 31132200 31132200 31132200 AATGATCTTCTTTCTTGGCTTCCAAAAGTGCTAGGATTACAGGCGTGAGCCACTGTGGCTGGCCT AATGATCTTCTTTCTTGGCTTCCAAAAGTGCTGGGATTACAGGCGTGAGCCACTGTGGCTGGCCT A G NF1 Ensembl:ENSG00000196712 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs567085455 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183307,RMVar_hsa_circ_95146 50040 RMVar_ID_50040 Human_SNP_ID_621826474 A-to-I Human chr17 + 31189841 31189840 31189841 TGGAGTGCAATGGCACAATCTCCGCTTAGTGCAACCCCCGCCTCTCGGGTTCAAGCGATTCTCCT TGGAGTGCAATGGCACAATCTCCGCTTAGTGC_ACCCCCGCCTCTCGGGTTCAAGCGATTCTCCT CA C NF1 Ensembl:ENSG00000196712 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1161284101 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_135,RMVar_hsa_circ_183310,RMVar_hsa_circ_276888,RMVar_hsa_circ_183307,RMVar_hsa_circ_95146,RMVar_hsa_circ_343584,RMVar_hsa_circ_351530,RMVar_hsa_circ_367536,RMVar_hsa_circ_282364,RMVar_hsa_circ_114262,RMVar_hsa_circ_12203,RMVar_hsa_circ_30521,RMVar_hsa_circ_42526,RMVar_hsa_circ_27234,RMVar_hsa_circ_183311,RMVar_hsa_circ_88847,RMVar_hsa_circ_183308,RMVar_hsa_circ_183309,RMVar_hsa_circ_183320,RMVar_hsa_circ_332916,RMVar_hsa_circ_294759,RMVar_hsa_circ_282731,RMVar_hsa_circ_26294,RMVar_hsa_circ_183328,RMVar_hsa_circ_110409,RMVar_hsa_circ_183322,RMVar_hsa_circ_183323,RMVar_hsa_circ_293296,RMVar_hsa_circ_370432,RMVar_hsa_circ_183321,RMVar_hsa_circ_318865,RMVar_hsa_circ_1137,RMVar_hsa_circ_8453,RMVar_hsa_circ_183330,RMVar_hsa_circ_183331,RMVar_hsa_circ_183329,RMVar_hsa_circ_79241,RMVar_hsa_circ_183333,RMVar_hsa_circ_282649,RMVar_hsa_circ_325080,RMVar_hsa_circ_332820,RMVar_hsa_circ_31174,RMVar_hsa_circ_183332,RMVar_hsa_circ_183336 50041 RMVar_ID_50041 Human_SNP_ID_621826475 A-to-I Human chr17 + 31189841 31189841 31189841 TGGAGTGCAATGGCACAATCTCCGCTTAGTGCAACCCCCGCCTCTCGGGTTCAAGCGATTCTCCT TGGAGTGCAATGGCACAATCTCCGCTTAGTGCGACCCCCGCCTCTCGGGTTCAAGCGATTCTCCT A G NF1 Ensembl:ENSG00000196712 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1373190348 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_135,RMVar_hsa_circ_183310,RMVar_hsa_circ_276888,RMVar_hsa_circ_183307,RMVar_hsa_circ_95146,RMVar_hsa_circ_343584,RMVar_hsa_circ_351530,RMVar_hsa_circ_367536,RMVar_hsa_circ_282364,RMVar_hsa_circ_114262,RMVar_hsa_circ_12203,RMVar_hsa_circ_30521,RMVar_hsa_circ_42526,RMVar_hsa_circ_27234,RMVar_hsa_circ_183311,RMVar_hsa_circ_88847,RMVar_hsa_circ_183308,RMVar_hsa_circ_183309,RMVar_hsa_circ_183320,RMVar_hsa_circ_332916,RMVar_hsa_circ_294759,RMVar_hsa_circ_282731,RMVar_hsa_circ_26294,RMVar_hsa_circ_183328,RMVar_hsa_circ_110409,RMVar_hsa_circ_183322,RMVar_hsa_circ_183323,RMVar_hsa_circ_293296,RMVar_hsa_circ_370432,RMVar_hsa_circ_183321,RMVar_hsa_circ_318865,RMVar_hsa_circ_1137,RMVar_hsa_circ_8453,RMVar_hsa_circ_183330,RMVar_hsa_circ_183331,RMVar_hsa_circ_183329,RMVar_hsa_circ_79241,RMVar_hsa_circ_183333,RMVar_hsa_circ_282649,RMVar_hsa_circ_325080,RMVar_hsa_circ_332820,RMVar_hsa_circ_31174,RMVar_hsa_circ_183332,RMVar_hsa_circ_183336 50042 RMVar_ID_50042 Human_SNP_ID_621848927 A-to-I Human chr17 + 31283682 31283682 31283682 GTCTAGCTGATTTTTGTATTTTTTGTAGAGACAGGGTTTGTCATGTTGCCCAGGCTGATCTCAAG GTCTAGCTGATTTTTGTATTTTTTGTAGAGACGGGGTTTGTCATGTTGCCCAGGCTGATCTCAAG A G NF1 Ensembl:ENSG00000196712 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs755560803 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17565852 RMVar_hsa_circ_183307,RMVar_hsa_circ_95146,RMVar_hsa_circ_79241,RMVar_hsa_circ_103532,RMVar_hsa_circ_183336,RMVar_hsa_circ_45175,RMVar_hsa_circ_183337,RMVar_hsa_circ_119184,RMVar_hsa_circ_183346,RMVar_hsa_circ_80029,RMVar_hsa_circ_65625,RMVar_hsa_circ_183351,RMVar_hsa_circ_101478,RMVar_hsa_circ_110610,RMVar_hsa_circ_183357,RMVar_hsa_circ_121698,RMVar_hsa_circ_183358,RMVar_hsa_circ_93308,RMVar_hsa_circ_109196,RMVar_hsa_circ_183359,RMVar_hsa_circ_183360,RMVar_hsa_circ_118493,RMVar_hsa_circ_121821,RMVar_hsa_circ_183362,RMVar_hsa_circ_183363,RMVar_hsa_circ_183364,RMVar_hsa_circ_21347,RMVar_hsa_circ_84277,RMVar_hsa_circ_85069,RMVar_hsa_circ_183365,RMVar_hsa_circ_183366,RMVar_hsa_circ_93524,RMVar_hsa_circ_112888,RMVar_hsa_circ_18669,RMVar_hsa_circ_183369,RMVar_hsa_circ_96941,RMVar_hsa_circ_183371,RMVar_hsa_circ_36427,RMVar_hsa_circ_264928,RMVar_hsa_circ_101265,RMVar_hsa_circ_6440,RMVar_hsa_circ_183373,RMVar_hsa_circ_183376,RMVar_hsa_circ_320069,RMVar_hsa_circ_98346,RMVar_hsa_circ_183380,RMVar_hsa_circ_48454,RMVar_hsa_circ_374846,RMVar_hsa_circ_107086,RMVar_hsa_circ_117270,RMVar_hsa_circ_50975,RMVar_hsa_circ_183385,RMVar_hsa_circ_183381,RMVar_hsa_circ_183383,RMVar_hsa_circ_183382,RMVar_hsa_circ_123095 50043 RMVar_ID_50043 Human_SNP_ID_621848944 A-to-I Human chr17 + 31283768 31283768 31283768 CCTTGGCGTCCCAAAGTGTTAGGATTACAGGCATGAGCCACCTTATTAGGCCTAATTACCAGTTT CCTTGGCGTCCCAAAGTGTTAGGATTACAGGCGTGAGCCACCTTATTAGGCCTAATTACCAGTTT A G NF1 Ensembl:ENSG00000196712 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs952256048 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183307,RMVar_hsa_circ_95146,RMVar_hsa_circ_79241,RMVar_hsa_circ_103532,RMVar_hsa_circ_183336,RMVar_hsa_circ_45175,RMVar_hsa_circ_183337,RMVar_hsa_circ_119184,RMVar_hsa_circ_183346,RMVar_hsa_circ_80029,RMVar_hsa_circ_65625,RMVar_hsa_circ_183351,RMVar_hsa_circ_101478,RMVar_hsa_circ_110610,RMVar_hsa_circ_183357,RMVar_hsa_circ_121698,RMVar_hsa_circ_183358,RMVar_hsa_circ_93308,RMVar_hsa_circ_109196,RMVar_hsa_circ_183359,RMVar_hsa_circ_183360,RMVar_hsa_circ_118493,RMVar_hsa_circ_121821,RMVar_hsa_circ_183362,RMVar_hsa_circ_183363,RMVar_hsa_circ_183364,RMVar_hsa_circ_21347,RMVar_hsa_circ_84277,RMVar_hsa_circ_85069,RMVar_hsa_circ_183365,RMVar_hsa_circ_183366,RMVar_hsa_circ_93524,RMVar_hsa_circ_112888,RMVar_hsa_circ_18669,RMVar_hsa_circ_183369,RMVar_hsa_circ_96941,RMVar_hsa_circ_183371,RMVar_hsa_circ_36427,RMVar_hsa_circ_264928,RMVar_hsa_circ_101265,RMVar_hsa_circ_6440,RMVar_hsa_circ_183373,RMVar_hsa_circ_183376,RMVar_hsa_circ_320069,RMVar_hsa_circ_98346,RMVar_hsa_circ_183380,RMVar_hsa_circ_48454,RMVar_hsa_circ_374846,RMVar_hsa_circ_107086,RMVar_hsa_circ_117270,RMVar_hsa_circ_50975,RMVar_hsa_circ_183385,RMVar_hsa_circ_183381,RMVar_hsa_circ_183383,RMVar_hsa_circ_183382,RMVar_hsa_circ_123095 50044 RMVar_ID_50044 Human_SNP_ID_621859359 A-to-I Human chr17 + 31326438 31326438 31326438 GGGATGTCAAGGTGGGCAGATCACGTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACACGGTGA GGGATGTCAAGGTGGGCAGATCACGTGAGGTCTGGAGTTCAAGACCAGCCTGGCCAACACGGTGA A T NF1 Ensembl:ENSG00000196712 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs986953411 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183307,RMVar_hsa_circ_95146,RMVar_hsa_circ_79241,RMVar_hsa_circ_103532,RMVar_hsa_circ_183336,RMVar_hsa_circ_45175,RMVar_hsa_circ_183337,RMVar_hsa_circ_119184,RMVar_hsa_circ_183346,RMVar_hsa_circ_80029,RMVar_hsa_circ_183351,RMVar_hsa_circ_101478,RMVar_hsa_circ_110610,RMVar_hsa_circ_183357,RMVar_hsa_circ_121698,RMVar_hsa_circ_183358,RMVar_hsa_circ_93308,RMVar_hsa_circ_109196,RMVar_hsa_circ_183359,RMVar_hsa_circ_183360,RMVar_hsa_circ_118493,RMVar_hsa_circ_121821,RMVar_hsa_circ_183362,RMVar_hsa_circ_183363,RMVar_hsa_circ_183364,RMVar_hsa_circ_21347,RMVar_hsa_circ_84277,RMVar_hsa_circ_85069,RMVar_hsa_circ_183365,RMVar_hsa_circ_183366,RMVar_hsa_circ_112888,RMVar_hsa_circ_183369,RMVar_hsa_circ_96941,RMVar_hsa_circ_36427,RMVar_hsa_circ_264928,RMVar_hsa_circ_101265,RMVar_hsa_circ_183373,RMVar_hsa_circ_183376,RMVar_hsa_circ_98346,RMVar_hsa_circ_183380,RMVar_hsa_circ_48454,RMVar_hsa_circ_106149,RMVar_hsa_circ_374846,RMVar_hsa_circ_117270,RMVar_hsa_circ_50975,RMVar_hsa_circ_183385,RMVar_hsa_circ_183381,RMVar_hsa_circ_183382,RMVar_hsa_circ_123095,RMVar_hsa_circ_304457,RMVar_hsa_circ_332995,RMVar_hsa_circ_352115,RMVar_hsa_circ_306247,RMVar_hsa_circ_183388,RMVar_hsa_circ_183389,RMVar_hsa_circ_183390,RMVar_hsa_circ_183387 50045 RMVar_ID_50045 Human_SNP_ID_621914782 A-to-I Human chr17 - 31548741 31548741 31548741 TCACTCCAACCTCCACCTCCCGGATCCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGA TCACTCCAACCTCCACCTCCCGGATCCAAGCAGTTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGA T C lnc-EVI2A-3,lnc-EVI2A-3:2 RNACentral:URS0000D5A877,RNACentral:URS0000D5AD58 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1266306504 Functional Loss SNV dbSNP153 33..33 33 - - - 50046 RMVar_ID_50046 Human_SNP_ID_621914798 A-to-I Human chr17 - 31548789 31548782 31548790 ACAGAGTCTTGCTCTGCCCAGGCTGGAGTGCAATGGCACGATCTCGGCTCACTCCAACCTCCACC ACAGAGTCTTGCTCTGCCCAGGCTGGAGTGC________GATCTCGGCTCACTCCAACCTCCACC CGTGCCATT C lnc-EVI2A-3,lnc-EVI2A-3:2 RNACentral:URS0000D5A877,RNACentral:URS0000D5AD58 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1236126393 Functional Loss DEL dbSNP153 32..39 33 - - - 50047 RMVar_ID_50047 Human_SNP_ID_621914801 A-to-I Human chr17 - 31548789 31548789 31548789 ACAGAGTCTTGCTCTGCCCAGGCTGGAGTGCAATGGCACGATCTCGGCTCACTCCAACCTCCACC ACAGAGTCTTGCTCTGCCCAGGCTGGAGTGCAGTGGCACGATCTCGGCTCACTCCAACCTCCACC T C lnc-EVI2A-3,lnc-EVI2A-3:2 RNACentral:URS0000D5A877,RNACentral:URS0000D5AD58 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1390032518 Functional Loss SNV dbSNP153 33..33 33 - - - 50048 RMVar_ID_50048 Human_SNP_ID_621921111 A-to-I Human chr17 + 31572211 31572211 31572211 GTATGAATATTCACACTCCCCAGGATAAATATAGACTCGAAATAATAGTTTCTAGTCAGTTTGGG GTATGAATATTCACACTCCCCAGGATAAATATTGACTCGAAATAATAGTTTCTAGTCAGTTTGGG A T AC003101.1 Ensembl:ENSG00000228768 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1057090749 Functional Loss SNV dbSNP153 33..33 33 - - - 50049 RMVar_ID_50049 Human_SNP_ID_621991454 A-to-I Human chr17 - 31854221 31854221 31854221 GGATTACAGGTGCATGCCACTGCACCCAGCTAAATTTTTTGAATTTTTTGTAGAGACAGGGTTTG GGATTACAGGTGCATGCCACTGCACCCAGCTACATTTTTTGAATTTTTTGTAGAGACAGGGTTTG T G COPRS Ensembl:ENSG00000172301 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350226456 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_119121,RMVar_hsa_circ_183410 50050 RMVar_ID_50050 Human_SNP_ID_621993412 A-to-I Human chr17 - 31861584 31861584 31861584 ATTGGACAAGTTCTTGCTTTGTCACCTAGGCTAGAGTGCAGTGGTGTGATCATGGCTCACTACAG ATTGGACAAGTTCTTGCTTTGTCACCTAGGCTGGAGTGCAGTGGTGTGATCATGGCTCACTACAG T C UTP6 Ensembl:ENSG00000108651 Protein coding 3'UTR GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1007035742 Functional Loss SNV dbSNP153 33..33 33 - - - 50051 RMVar_ID_50051 Human_SNP_ID_621994226 A-to-I Human chr17 - 31864655 31864655 31864655 TGCCACCATTGTACTCCAGCCTGGGCAATACAATGAGATCCTGTCTCAAAAACAAAAACCAAAAA TGCCACCATTGTACTCCAGCCTGGGCAATACAGTGAGATCCTGTCTCAAAAACAAAAACCAAAAA T C UTP6 Ensembl:ENSG00000108651 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1030806874 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183412,RMVar_hsa_circ_122111 50052 RMVar_ID_50052 Human_SNP_ID_621996910 A-to-I Human chr17 - 31874721 31874721 31874721 CTCCATGTTGGCCAGGCTGGTCTGGAACTCCTAGCCTCAAGTGATCTGCCCGCCTTGGCCTCCCA CTCCATGTTGGCCAGGCTGGTCTGGAACTCCTGGCCTCAAGTGATCTGCCCGCCTTGGCCTCCCA T C UTP6 Ensembl:ENSG00000108651 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1238756604 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12962915 RMVar_hsa_circ_18385,RMVar_hsa_circ_95871,RMVar_hsa_circ_336674,RMVar_hsa_circ_342168,RMVar_hsa_circ_34566,RMVar_hsa_circ_183414,RMVar_hsa_circ_183415,RMVar_hsa_circ_6658,RMVar_hsa_circ_353194 50053 RMVar_ID_50053 Human_SNP_ID_621996920 A-to-I Human chr17 - 31874766 31874766 31874766 CATCACACCTGACTAATATTTTCTATTTTAGTAGAGACAGGATATCTCCATGTTGGCCAGGCTGG CATCACACCTGACTAATATTTTCTATTTTAGTGGAGACAGGATATCTCCATGTTGGCCAGGCTGG T C UTP6 Ensembl:ENSG00000108651 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1350613256 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18385,RMVar_hsa_circ_95871,RMVar_hsa_circ_336674,RMVar_hsa_circ_342168,RMVar_hsa_circ_34566,RMVar_hsa_circ_183414,RMVar_hsa_circ_183415,RMVar_hsa_circ_6658,RMVar_hsa_circ_353194 50054 RMVar_ID_50054 Human_SNP_ID_621997284 A-to-I Human chr17 - 31876129 31876129 31876129 GGGAGGCTGAGGGAGGAGAATTGCTTGAACCCAGGAGTTGGAGGTTGCAGTGAGCCGAGATCATT GGGAGGCTGAGGGAGGAGAATTGCTTGAACCCGGGAGTTGGAGGTTGCAGTGAGCCGAGATCATT T C UTP6 Ensembl:ENSG00000108651 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1010544603 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18385,RMVar_hsa_circ_95871,RMVar_hsa_circ_336674,RMVar_hsa_circ_34566,RMVar_hsa_circ_99511,RMVar_hsa_circ_183414,RMVar_hsa_circ_183415,RMVar_hsa_circ_6658,RMVar_hsa_circ_353194,RMVar_hsa_circ_51837,RMVar_hsa_circ_64841,RMVar_hsa_circ_183416 50055 RMVar_ID_50055 Human_SNP_ID_621998082 A-to-I Human chr17 - 31879407 31879407 31879407 CCTCGGCCTCCCAACTTGCTAGGATTACCGACATCCTTAATTATCTTTTTGAGACAGAGTCTCAC CCTCGGCCTCCCAACTTGCTAGGATTACCGACTTCCTTAATTATCTTTTTGAGACAGAGTCTCAC T A UTP6 Ensembl:ENSG00000108651 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11658469 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8449217 GWAS_ID_6328,GWAS_ID_6329,GWAS_ID_6330,GWAS_ID_6331,GWAS_ID_6332,GWAS_ID_6333,GWAS_ID_6334,GWAS_ID_6335,GWAS_ID_6336,GWAS_ID_6337,GWAS_ID_6338,GWAS_ID_6339,GWAS_ID_6340,GWAS_ID_6341,GWAS_ID_6342,GWAS_ID_6343,GWAS_ID_6344,GWAS_ID_6345,GWAS_ID_6346,GWAS_ID_6347,GWAS_ID_6348,GWAS_ID_6349,GWAS_ID_6350,GWAS_ID_6351,GWAS_ID_6352,GWAS_ID_6353 RMVar_hsa_circ_18385,RMVar_hsa_circ_95871,RMVar_hsa_circ_8176,RMVar_hsa_circ_183415,RMVar_hsa_circ_6658,RMVar_hsa_circ_353194,RMVar_hsa_circ_298755,RMVar_hsa_circ_51837,RMVar_hsa_circ_64841,RMVar_hsa_circ_332632,RMVar_hsa_circ_329041,RMVar_hsa_circ_99101,RMVar_hsa_circ_64596,RMVar_hsa_circ_267971,RMVar_hsa_circ_183418,RMVar_hsa_circ_183419 50056 RMVar_ID_50056 Human_SNP_ID_621998083 A-to-I Human chr17 - 31879407 31879407 31879407 CCTCGGCCTCCCAACTTGCTAGGATTACCGACATCCTTAATTATCTTTTTGAGACAGAGTCTCAC CCTCGGCCTCCCAACTTGCTAGGATTACCGACGTCCTTAATTATCTTTTTGAGACAGAGTCTCAC T C UTP6 Ensembl:ENSG00000108651 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11658469 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8449217 GWAS_ID_6328,GWAS_ID_6329,GWAS_ID_6330,GWAS_ID_6331,GWAS_ID_6332,GWAS_ID_6333,GWAS_ID_6334,GWAS_ID_6335,GWAS_ID_6336,GWAS_ID_6337,GWAS_ID_6338,GWAS_ID_6339,GWAS_ID_6340,GWAS_ID_6341,GWAS_ID_6342,GWAS_ID_6343,GWAS_ID_6344,GWAS_ID_6345,GWAS_ID_6346,GWAS_ID_6347,GWAS_ID_6348,GWAS_ID_6349,GWAS_ID_6350,GWAS_ID_6351,GWAS_ID_6352,GWAS_ID_6353 RMVar_hsa_circ_18385,RMVar_hsa_circ_95871,RMVar_hsa_circ_8176,RMVar_hsa_circ_183415,RMVar_hsa_circ_6658,RMVar_hsa_circ_353194,RMVar_hsa_circ_298755,RMVar_hsa_circ_51837,RMVar_hsa_circ_64841,RMVar_hsa_circ_332632,RMVar_hsa_circ_329041,RMVar_hsa_circ_99101,RMVar_hsa_circ_64596,RMVar_hsa_circ_267971,RMVar_hsa_circ_183418,RMVar_hsa_circ_183419 50057 RMVar_ID_50057 Human_SNP_ID_621999686 A-to-I Human chr17 - 31885605 31885605 31885605 TTTTGTATTTTTAGTAGAGACGTAGTTTCACTATGTTGGCTAGGCTGGTCTCGTACTCCTGACCT TTTTGTATTTTTAGTAGAGACGTAGTTTCACTTTGTTGGCTAGGCTGGTCTCGTACTCCTGACCT T A UTP6 Ensembl:ENSG00000108651 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs962418724 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8176,RMVar_hsa_circ_64841,RMVar_hsa_circ_329041,RMVar_hsa_circ_99101,RMVar_hsa_circ_64596,RMVar_hsa_circ_183421,RMVar_hsa_circ_267971,RMVar_hsa_circ_183419,RMVar_hsa_circ_81138,RMVar_hsa_circ_349140,RMVar_hsa_circ_365759,RMVar_hsa_circ_274831,RMVar_hsa_circ_46530,RMVar_hsa_circ_183422,RMVar_hsa_circ_183423,RMVar_hsa_circ_61878,RMVar_hsa_circ_311791,RMVar_hsa_circ_325381,RMVar_hsa_circ_316192,RMVar_hsa_circ_282778,RMVar_hsa_circ_183424,RMVar_hsa_circ_183425 50058 RMVar_ID_50058 Human_SNP_ID_621999687 A-to-I Human chr17 - 31885605 31885605 31885605 TTTTGTATTTTTAGTAGAGACGTAGTTTCACTATGTTGGCTAGGCTGGTCTCGTACTCCTGACCT TTTTGTATTTTTAGTAGAGACGTAGTTTCACTGTGTTGGCTAGGCTGGTCTCGTACTCCTGACCT T C UTP6 Ensembl:ENSG00000108651 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs962418724 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8176,RMVar_hsa_circ_64841,RMVar_hsa_circ_329041,RMVar_hsa_circ_99101,RMVar_hsa_circ_64596,RMVar_hsa_circ_183421,RMVar_hsa_circ_267971,RMVar_hsa_circ_183419,RMVar_hsa_circ_81138,RMVar_hsa_circ_349140,RMVar_hsa_circ_365759,RMVar_hsa_circ_274831,RMVar_hsa_circ_46530,RMVar_hsa_circ_183422,RMVar_hsa_circ_183423,RMVar_hsa_circ_61878,RMVar_hsa_circ_311791,RMVar_hsa_circ_325381,RMVar_hsa_circ_316192,RMVar_hsa_circ_282778,RMVar_hsa_circ_183424,RMVar_hsa_circ_183425 50059 RMVar_ID_50059 Human_SNP_ID_622002621 A-to-I Human chr17 - 31896844 31896844 31896844 ATCGCTTGAGCCCAGGAGTTCAAGACCAGCCTAGGCAACATGGCAAACCCCATCTCTACAAAAAA ATCGCTTGAGCCCAGGAGTTCAAGACCAGCCTGGGCAACATGGCAAACCCCATCTCTACAAAAAA T C UTP6 Ensembl:ENSG00000108651 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1398514883 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6244,RMVar_hsa_circ_349140,RMVar_hsa_circ_183423,RMVar_hsa_circ_311791,RMVar_hsa_circ_378960,RMVar_hsa_circ_338393 50060 RMVar_ID_50060 Human_SNP_ID_622002682 A-to-I Human chr17 - 31897115 31897115 31897115 GGCTGGCTAATTTTCTTATTTTTTGTAGAGATAGGGTCTCCTTATGTTGCCCAGGCTGGTCTTGA GGCTGGCTAATTTTCTTATTTTTTGTAGAGATGGGGTCTCCTTATGTTGCCCAGGCTGGTCTTGA T C UTP6 Ensembl:ENSG00000108651 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs946124057 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6244,RMVar_hsa_circ_349140,RMVar_hsa_circ_183423,RMVar_hsa_circ_311791,RMVar_hsa_circ_378960,RMVar_hsa_circ_338393 50061 RMVar_ID_50061 Human_SNP_ID_622003022 A-to-I Human chr17 - 31898442 31898442 31898442 CGGCTCACTGCAACCTCCGCTTCCTGGGTTCAAGCAGTTATCTGCCTCAGCCTCCTGAGTAGCTG CGGCTCACTGCAACCTCCGCTTCCTGGGTTCAGGCAGTTATCTGCCTCAGCCTCCTGAGTAGCTG T C UTP6 Ensembl:ENSG00000108651 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1418762951 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6244,RMVar_hsa_circ_349140,RMVar_hsa_circ_183423,RMVar_hsa_circ_311791,RMVar_hsa_circ_378960,RMVar_hsa_circ_338393 50062 RMVar_ID_50062 Human_SNP_ID_622003271 A-to-I Human chr17 - 31899491 31899491 31899491 ACCTCTGCCCTCCAGGCTCAAGCGATTCTCCTACCTCAGCCTCCTGGGTAGCTGGGACCATAGAT ACCTCTGCCCTCCAGGCTCAAGCGATTCTCCTGCCTCAGCCTCCTGGGTAGCTGGGACCATAGAT T C UTP6 Ensembl:ENSG00000108651 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1021386545 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25269802 RMVar_hsa_circ_6244,RMVar_hsa_circ_349140,RMVar_hsa_circ_183423,RMVar_hsa_circ_311791,RMVar_hsa_circ_378960,RMVar_hsa_circ_338393 50063 RMVar_ID_50063 Human_SNP_ID_622003272 A-to-I Human chr17 - 31899491 31899491 31899491 ACCTCTGCCCTCCAGGCTCAAGCGATTCTCCTACCTCAGCCTCCTGGGTAGCTGGGACCATAGAT ACCTCTGCCCTCCAGGCTCAAGCGATTCTCCTCCCTCAGCCTCCTGGGTAGCTGGGACCATAGAT T G UTP6 Ensembl:ENSG00000108651 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1021386545 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25269802 RMVar_hsa_circ_6244,RMVar_hsa_circ_349140,RMVar_hsa_circ_183423,RMVar_hsa_circ_311791,RMVar_hsa_circ_378960,RMVar_hsa_circ_338393 50064 RMVar_ID_50064 Human_SNP_ID_622016662 A-to-I Human chr17 + 31949761 31949761 31949761 AGGCTGGAGTGCAGTGGCGCGATCTTGGCTCTACAGCCTCCACCTCCCGGGCTCAAGCAATTCAC AGGCTGGAGTGCAGTGGCGCGATCTTGGCTCTGCAGCCTCCACCTCCCGGGCTCAAGCAATTCAC A G SUZ12 Ensembl:ENSG00000178691 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1297213980 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6581727,Human_RBP_ID_12963806 RMVar_hsa_circ_183432,RMVar_hsa_circ_82540,RMVar_hsa_circ_107506,RMVar_hsa_circ_183431,RMVar_hsa_circ_308935,RMVar_hsa_circ_374863,RMVar_hsa_circ_376997,RMVar_hsa_circ_346657,RMVar_hsa_circ_308402,RMVar_hsa_circ_281629,RMVar_hsa_circ_296603,RMVar_hsa_circ_282017,RMVar_hsa_circ_111477,RMVar_hsa_circ_114951,RMVar_hsa_circ_101296,RMVar_hsa_circ_183436,RMVar_hsa_circ_183440,RMVar_hsa_circ_183442,RMVar_hsa_circ_183441,RMVar_hsa_circ_183438,RMVar_hsa_circ_183439,RMVar_hsa_circ_183437,RMVar_hsa_circ_183434,RMVar_hsa_circ_183435,RMVar_hsa_circ_183433,RMVar_hsa_circ_271257,RMVar_hsa_circ_21745,RMVar_hsa_circ_269028,RMVar_hsa_circ_55965,RMVar_hsa_circ_336062,RMVar_hsa_circ_359482,RMVar_hsa_circ_286697,RMVar_hsa_circ_49798 50065 RMVar_ID_50065 Human_SNP_ID_622020216 A-to-I Human chr17 + 31962467 31962467 31962467 TAAAAATTAGCCAGGCATGATGGTGCATGCCTATAGTCTCAGCTACTCTTGGAGGCTGAGGTGGG TAAAAATTAGCCAGGCATGATGGTGCATGCCTGTAGTCTCAGCTACTCTTGGAGGCTGAGGTGGG A G SUZ12 Ensembl:ENSG00000178691 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs483692 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25270005 RMVar_hsa_circ_183432,RMVar_hsa_circ_82540,RMVar_hsa_circ_107506,RMVar_hsa_circ_183431,RMVar_hsa_circ_308935,RMVar_hsa_circ_374863,RMVar_hsa_circ_376997,RMVar_hsa_circ_346657,RMVar_hsa_circ_308402,RMVar_hsa_circ_281629,RMVar_hsa_circ_296603,RMVar_hsa_circ_282017,RMVar_hsa_circ_111477,RMVar_hsa_circ_114951,RMVar_hsa_circ_101296,RMVar_hsa_circ_183436,RMVar_hsa_circ_183440,RMVar_hsa_circ_183442,RMVar_hsa_circ_183441,RMVar_hsa_circ_183438,RMVar_hsa_circ_183439,RMVar_hsa_circ_183437,RMVar_hsa_circ_183434,RMVar_hsa_circ_183435,RMVar_hsa_circ_183433,RMVar_hsa_circ_271257,RMVar_hsa_circ_21745,RMVar_hsa_circ_269028,RMVar_hsa_circ_55965,RMVar_hsa_circ_336062,RMVar_hsa_circ_359482,RMVar_hsa_circ_286697,RMVar_hsa_circ_49798 50066 RMVar_ID_50066 Human_SNP_ID_622020483 A-to-I Human chr17 + 31963284 31963284 31963284 CTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCGCATGCCACAACGCCTGGCTAATTTTG CTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTGCAGGCGCATGCCACAACGCCTGGCTAATTTTG A G SUZ12 Ensembl:ENSG00000178691 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1365408295 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183432,RMVar_hsa_circ_82540,RMVar_hsa_circ_107506,RMVar_hsa_circ_183431,RMVar_hsa_circ_308935,RMVar_hsa_circ_374863,RMVar_hsa_circ_376997,RMVar_hsa_circ_346657,RMVar_hsa_circ_308402,RMVar_hsa_circ_281629,RMVar_hsa_circ_296603,RMVar_hsa_circ_282017,RMVar_hsa_circ_111477,RMVar_hsa_circ_114951,RMVar_hsa_circ_101296,RMVar_hsa_circ_183436,RMVar_hsa_circ_183440,RMVar_hsa_circ_183442,RMVar_hsa_circ_183441,RMVar_hsa_circ_183438,RMVar_hsa_circ_183439,RMVar_hsa_circ_183437,RMVar_hsa_circ_183434,RMVar_hsa_circ_183435,RMVar_hsa_circ_183433,RMVar_hsa_circ_271257,RMVar_hsa_circ_21745,RMVar_hsa_circ_269028,RMVar_hsa_circ_55965,RMVar_hsa_circ_336062,RMVar_hsa_circ_359482,RMVar_hsa_circ_286697,RMVar_hsa_circ_49798 50067 RMVar_ID_50067 Human_SNP_ID_622021637 A-to-I Human chr17 + 31967018 31967018 31967018 TCAGGAGTTCAGGAGTTCAGCTGGCCAATATGATGAAACCCCATCTCTACTAAAAATATAAACAT TCAGGAGTTCAGGAGTTCAGCTGGCCAATATGGTGAAACCCCATCTCTACTAAAAATATAAACAT A G SUZ12 Ensembl:ENSG00000178691 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1225143456 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183432,RMVar_hsa_circ_82540,RMVar_hsa_circ_107506,RMVar_hsa_circ_183431,RMVar_hsa_circ_308935,RMVar_hsa_circ_374863,RMVar_hsa_circ_376997,RMVar_hsa_circ_346657,RMVar_hsa_circ_308402,RMVar_hsa_circ_296603,RMVar_hsa_circ_282017,RMVar_hsa_circ_111477,RMVar_hsa_circ_114951,RMVar_hsa_circ_101296,RMVar_hsa_circ_183436,RMVar_hsa_circ_183440,RMVar_hsa_circ_183441,RMVar_hsa_circ_183438,RMVar_hsa_circ_183439,RMVar_hsa_circ_183437,RMVar_hsa_circ_183434,RMVar_hsa_circ_183435,RMVar_hsa_circ_183433,RMVar_hsa_circ_27202,RMVar_hsa_circ_271257,RMVar_hsa_circ_21745,RMVar_hsa_circ_269028,RMVar_hsa_circ_55965,RMVar_hsa_circ_336062,RMVar_hsa_circ_359482,RMVar_hsa_circ_286697,RMVar_hsa_circ_116846,RMVar_hsa_circ_297913,RMVar_hsa_circ_355615,RMVar_hsa_circ_49798,RMVar_hsa_circ_306517,RMVar_hsa_circ_295905,RMVar_hsa_circ_81874,RMVar_hsa_circ_183447,RMVar_hsa_circ_183448,RMVar_hsa_circ_183449,RMVar_hsa_circ_183446 50068 RMVar_ID_50068 Human_SNP_ID_622021665 A-to-I Human chr17 + 31967114 31967114 31967114 CCAGTTACTTGGGAGACTTAGGCAGAAGAATCACTTGAACCTGAGAGTCGGAGGTTGCAATGAGC CCAGTTACTTGGGAGACTTAGGCAGAAGAATCGCTTGAACCTGAGAGTCGGAGGTTGCAATGAGC A G SUZ12 Ensembl:ENSG00000178691 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs532108818 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12964186,Human_RBP_ID_17565856 RMVar_hsa_circ_183432,RMVar_hsa_circ_82540,RMVar_hsa_circ_107506,RMVar_hsa_circ_183431,RMVar_hsa_circ_308935,RMVar_hsa_circ_374863,RMVar_hsa_circ_376997,RMVar_hsa_circ_346657,RMVar_hsa_circ_308402,RMVar_hsa_circ_296603,RMVar_hsa_circ_282017,RMVar_hsa_circ_111477,RMVar_hsa_circ_114951,RMVar_hsa_circ_101296,RMVar_hsa_circ_183436,RMVar_hsa_circ_183440,RMVar_hsa_circ_183441,RMVar_hsa_circ_183438,RMVar_hsa_circ_183439,RMVar_hsa_circ_183437,RMVar_hsa_circ_183434,RMVar_hsa_circ_183435,RMVar_hsa_circ_183433,RMVar_hsa_circ_27202,RMVar_hsa_circ_271257,RMVar_hsa_circ_21745,RMVar_hsa_circ_269028,RMVar_hsa_circ_55965,RMVar_hsa_circ_336062,RMVar_hsa_circ_359482,RMVar_hsa_circ_286697,RMVar_hsa_circ_116846,RMVar_hsa_circ_297913,RMVar_hsa_circ_355615,RMVar_hsa_circ_49798,RMVar_hsa_circ_306517,RMVar_hsa_circ_295905,RMVar_hsa_circ_81874,RMVar_hsa_circ_183447,RMVar_hsa_circ_183448,RMVar_hsa_circ_183449,RMVar_hsa_circ_183446 50069 RMVar_ID_50069 Human_SNP_ID_622021666 A-to-I Human chr17 + 31967114 31967114 31967114 CCAGTTACTTGGGAGACTTAGGCAGAAGAATCACTTGAACCTGAGAGTCGGAGGTTGCAATGAGC CCAGTTACTTGGGAGACTTAGGCAGAAGAATCTCTTGAACCTGAGAGTCGGAGGTTGCAATGAGC A T SUZ12 Ensembl:ENSG00000178691 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs532108818 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12964186,Human_RBP_ID_17565856 RMVar_hsa_circ_183432,RMVar_hsa_circ_82540,RMVar_hsa_circ_107506,RMVar_hsa_circ_183431,RMVar_hsa_circ_308935,RMVar_hsa_circ_374863,RMVar_hsa_circ_376997,RMVar_hsa_circ_346657,RMVar_hsa_circ_308402,RMVar_hsa_circ_296603,RMVar_hsa_circ_282017,RMVar_hsa_circ_111477,RMVar_hsa_circ_114951,RMVar_hsa_circ_101296,RMVar_hsa_circ_183436,RMVar_hsa_circ_183440,RMVar_hsa_circ_183441,RMVar_hsa_circ_183438,RMVar_hsa_circ_183439,RMVar_hsa_circ_183437,RMVar_hsa_circ_183434,RMVar_hsa_circ_183435,RMVar_hsa_circ_183433,RMVar_hsa_circ_27202,RMVar_hsa_circ_271257,RMVar_hsa_circ_21745,RMVar_hsa_circ_269028,RMVar_hsa_circ_55965,RMVar_hsa_circ_336062,RMVar_hsa_circ_359482,RMVar_hsa_circ_286697,RMVar_hsa_circ_116846,RMVar_hsa_circ_297913,RMVar_hsa_circ_355615,RMVar_hsa_circ_49798,RMVar_hsa_circ_306517,RMVar_hsa_circ_295905,RMVar_hsa_circ_81874,RMVar_hsa_circ_183447,RMVar_hsa_circ_183448,RMVar_hsa_circ_183449,RMVar_hsa_circ_183446 50070 RMVar_ID_50070 Human_SNP_ID_622021884 A-to-I Human chr17 + 31967909 31967909 31967909 AAATATTAGACTGGGCGTGGTGGCTCACAGCTATAACGTCAACACCTTGGGAGGCTGAGATGGAA AAATATTAGACTGGGCGTGGTGGCTCACAGCTGTAACGTCAACACCTTGGGAGGCTGAGATGGAA A G SUZ12 Ensembl:ENSG00000178691 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1371796905 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183432,RMVar_hsa_circ_82540,RMVar_hsa_circ_107506,RMVar_hsa_circ_183431,RMVar_hsa_circ_308935,RMVar_hsa_circ_374863,RMVar_hsa_circ_376997,RMVar_hsa_circ_346657,RMVar_hsa_circ_308402,RMVar_hsa_circ_296603,RMVar_hsa_circ_282017,RMVar_hsa_circ_111477,RMVar_hsa_circ_114951,RMVar_hsa_circ_101296,RMVar_hsa_circ_183436,RMVar_hsa_circ_183440,RMVar_hsa_circ_183441,RMVar_hsa_circ_183438,RMVar_hsa_circ_183439,RMVar_hsa_circ_183437,RMVar_hsa_circ_183434,RMVar_hsa_circ_183435,RMVar_hsa_circ_183433,RMVar_hsa_circ_27202,RMVar_hsa_circ_271257,RMVar_hsa_circ_21745,RMVar_hsa_circ_269028,RMVar_hsa_circ_55965,RMVar_hsa_circ_336062,RMVar_hsa_circ_359482,RMVar_hsa_circ_286697,RMVar_hsa_circ_116846,RMVar_hsa_circ_297913,RMVar_hsa_circ_355615,RMVar_hsa_circ_49798,RMVar_hsa_circ_306517,RMVar_hsa_circ_295905,RMVar_hsa_circ_81874,RMVar_hsa_circ_183447,RMVar_hsa_circ_183448,RMVar_hsa_circ_183449,RMVar_hsa_circ_183446 50071 RMVar_ID_50071 Human_SNP_ID_622023171 A-to-I Human chr17 + 31972581 31972581 31972581 CTACAGGCACATGACACCCACCACACCCAGCTAATTTTTTCACATTTTGTAGAGACGAGGTTTCT CTACAGGCACATGACACCCACCACACCCAGCTGATTTTTTCACATTTTGTAGAGACGAGGTTTCT A G SUZ12 Ensembl:ENSG00000178691 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs976553726 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12964229 RMVar_hsa_circ_183432,RMVar_hsa_circ_82540,RMVar_hsa_circ_107506,RMVar_hsa_circ_183431,RMVar_hsa_circ_308935,RMVar_hsa_circ_374863,RMVar_hsa_circ_376997,RMVar_hsa_circ_346657,RMVar_hsa_circ_308402,RMVar_hsa_circ_296603,RMVar_hsa_circ_282017,RMVar_hsa_circ_111477,RMVar_hsa_circ_114951,RMVar_hsa_circ_101296,RMVar_hsa_circ_183436,RMVar_hsa_circ_183440,RMVar_hsa_circ_183441,RMVar_hsa_circ_183438,RMVar_hsa_circ_183439,RMVar_hsa_circ_183437,RMVar_hsa_circ_183434,RMVar_hsa_circ_183435,RMVar_hsa_circ_183433,RMVar_hsa_circ_27202,RMVar_hsa_circ_271257,RMVar_hsa_circ_21745,RMVar_hsa_circ_269028,RMVar_hsa_circ_55965,RMVar_hsa_circ_336062,RMVar_hsa_circ_359482,RMVar_hsa_circ_286697,RMVar_hsa_circ_116846,RMVar_hsa_circ_297913,RMVar_hsa_circ_355615,RMVar_hsa_circ_49798,RMVar_hsa_circ_306517,RMVar_hsa_circ_295905,RMVar_hsa_circ_81874,RMVar_hsa_circ_183447,RMVar_hsa_circ_183448,RMVar_hsa_circ_183449,RMVar_hsa_circ_183446 50072 RMVar_ID_50072 Human_SNP_ID_622026179 A-to-I Human chr17 + 31983496 31983496 31983496 TAGAGACGGGGTTTGACCATGTTGGCCAGGCTAGTCTGGAACTCCTGACCTTGTGATCTGCCCAC TAGAGACGGGGTTTGACCATGTTGGCCAGGCTGGTCTGGAACTCCTGACCTTGTGATCTGCCCAC A G SUZ12 Ensembl:ENSG00000178691 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs56292830 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183432,RMVar_hsa_circ_82540,RMVar_hsa_circ_107506,RMVar_hsa_circ_183431,RMVar_hsa_circ_308935,RMVar_hsa_circ_374863,RMVar_hsa_circ_376997,RMVar_hsa_circ_308402,RMVar_hsa_circ_114951,RMVar_hsa_circ_101296,RMVar_hsa_circ_183436,RMVar_hsa_circ_183437,RMVar_hsa_circ_183434,RMVar_hsa_circ_183435,RMVar_hsa_circ_183433,RMVar_hsa_circ_8311,RMVar_hsa_circ_27202,RMVar_hsa_circ_269028,RMVar_hsa_circ_336062,RMVar_hsa_circ_116846,RMVar_hsa_circ_49798,RMVar_hsa_circ_306517,RMVar_hsa_circ_83378,RMVar_hsa_circ_183448,RMVar_hsa_circ_183449,RMVar_hsa_circ_325424,RMVar_hsa_circ_75775,RMVar_hsa_circ_183451,RMVar_hsa_circ_62157,RMVar_hsa_circ_353084,RMVar_hsa_circ_183450,RMVar_hsa_circ_379057,RMVar_hsa_circ_274016,RMVar_hsa_circ_112645,RMVar_hsa_circ_183452,RMVar_hsa_circ_183453,RMVar_hsa_circ_289974,RMVar_hsa_circ_183455,RMVar_hsa_circ_66247,RMVar_hsa_circ_281257,RMVar_hsa_circ_183454,RMVar_hsa_circ_93863,RMVar_hsa_circ_183456 50073 RMVar_ID_50073 Human_SNP_ID_622027053 A-to-I Human chr17 + 31986700 31986700 31986700 CAGCCTCCCAAGTAGCTGGGATTACAGGCGCCAGCCACCATGCCCAGCTAATTTTTTGTATTTTA CAGCCTCCCAAGTAGCTGGGATTACAGGCGCCGGCCACCATGCCCAGCTAATTTTTTGTATTTTA A G SUZ12 Ensembl:ENSG00000178691 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1186875941 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183432,RMVar_hsa_circ_82540,RMVar_hsa_circ_107506,RMVar_hsa_circ_183431,RMVar_hsa_circ_308935,RMVar_hsa_circ_374863,RMVar_hsa_circ_376997,RMVar_hsa_circ_308402,RMVar_hsa_circ_114951,RMVar_hsa_circ_101296,RMVar_hsa_circ_183436,RMVar_hsa_circ_183437,RMVar_hsa_circ_183434,RMVar_hsa_circ_183435,RMVar_hsa_circ_183433,RMVar_hsa_circ_8311,RMVar_hsa_circ_27202,RMVar_hsa_circ_269028,RMVar_hsa_circ_336062,RMVar_hsa_circ_116846,RMVar_hsa_circ_49798,RMVar_hsa_circ_306517,RMVar_hsa_circ_83378,RMVar_hsa_circ_183448,RMVar_hsa_circ_183449,RMVar_hsa_circ_325424,RMVar_hsa_circ_75775,RMVar_hsa_circ_183451,RMVar_hsa_circ_62157,RMVar_hsa_circ_353084,RMVar_hsa_circ_183450,RMVar_hsa_circ_379057,RMVar_hsa_circ_274016,RMVar_hsa_circ_112645,RMVar_hsa_circ_183452,RMVar_hsa_circ_183453,RMVar_hsa_circ_289974,RMVar_hsa_circ_183455,RMVar_hsa_circ_66247,RMVar_hsa_circ_281257,RMVar_hsa_circ_183454,RMVar_hsa_circ_93863,RMVar_hsa_circ_183456 50074 RMVar_ID_50074 Human_SNP_ID_622027313 A-to-I Human chr17 + 31987769 31987769 31987769 CCTGGCCAAGATGATGAAACCCCGTCTCTACTAAAAACACACACACAAAAAATTAGCTGGGCGTG CCTGGCCAAGATGATGAAACCCCGTCTCTACTGAAAACACACACACAAAAAATTAGCTGGGCGTG A G SUZ12 Ensembl:ENSG00000178691 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs545109320 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183432,RMVar_hsa_circ_82540,RMVar_hsa_circ_107506,RMVar_hsa_circ_183431,RMVar_hsa_circ_308935,RMVar_hsa_circ_374863,RMVar_hsa_circ_376997,RMVar_hsa_circ_308402,RMVar_hsa_circ_114951,RMVar_hsa_circ_101296,RMVar_hsa_circ_183436,RMVar_hsa_circ_183437,RMVar_hsa_circ_183434,RMVar_hsa_circ_183435,RMVar_hsa_circ_183433,RMVar_hsa_circ_8311,RMVar_hsa_circ_27202,RMVar_hsa_circ_269028,RMVar_hsa_circ_336062,RMVar_hsa_circ_116846,RMVar_hsa_circ_49798,RMVar_hsa_circ_306517,RMVar_hsa_circ_83378,RMVar_hsa_circ_183448,RMVar_hsa_circ_183449,RMVar_hsa_circ_325424,RMVar_hsa_circ_75775,RMVar_hsa_circ_183451,RMVar_hsa_circ_62157,RMVar_hsa_circ_353084,RMVar_hsa_circ_183450,RMVar_hsa_circ_379057,RMVar_hsa_circ_274016,RMVar_hsa_circ_112645,RMVar_hsa_circ_183452,RMVar_hsa_circ_183453,RMVar_hsa_circ_289974,RMVar_hsa_circ_183455,RMVar_hsa_circ_66247,RMVar_hsa_circ_281257,RMVar_hsa_circ_183454,RMVar_hsa_circ_93863,RMVar_hsa_circ_183456 50075 RMVar_ID_50075 Human_SNP_ID_622027583 A-to-I Human chr17 + 31988710 31988710 31988710 TGCCTTGTGGGTTCAGATGATTCTCCTGACTCAGCCTCCCGAGTAGCTGTGACTACAGGCGCATG TGCCTTGTGGGTTCAGATGATTCTCCTGACTCGGCCTCCCGAGTAGCTGTGACTACAGGCGCATG A G SUZ12 Ensembl:ENSG00000178691 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1345035819 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8449252,Human_RBP_ID_12964482 RMVar_hsa_circ_183432,RMVar_hsa_circ_82540,RMVar_hsa_circ_107506,RMVar_hsa_circ_183431,RMVar_hsa_circ_374863,RMVar_hsa_circ_376997,RMVar_hsa_circ_308402,RMVar_hsa_circ_114951,RMVar_hsa_circ_101296,RMVar_hsa_circ_183436,RMVar_hsa_circ_183434,RMVar_hsa_circ_183435,RMVar_hsa_circ_183433,RMVar_hsa_circ_8311,RMVar_hsa_circ_27202,RMVar_hsa_circ_269028,RMVar_hsa_circ_116846,RMVar_hsa_circ_49798,RMVar_hsa_circ_83378,RMVar_hsa_circ_183449,RMVar_hsa_circ_75775,RMVar_hsa_circ_183451,RMVar_hsa_circ_62157,RMVar_hsa_circ_353084,RMVar_hsa_circ_379057,RMVar_hsa_circ_112645,RMVar_hsa_circ_183452,RMVar_hsa_circ_66247,RMVar_hsa_circ_183454,RMVar_hsa_circ_93863,RMVar_hsa_circ_183456,RMVar_hsa_circ_183458,RMVar_hsa_circ_343959,RMVar_hsa_circ_352704,RMVar_hsa_circ_369532,RMVar_hsa_circ_314185,RMVar_hsa_circ_183460,RMVar_hsa_circ_121794,RMVar_hsa_circ_183459 50076 RMVar_ID_50076 Human_SNP_ID_622027616 A-to-I Human chr17 + 31988816 31988816 31988816 GGGTTGGCCGAGCGCAGTGGCTCAACACCTGTAATCTCAGCATTTGGGAGACCGAGGCGGGCGGA GGGTTGGCCGAGCGCAGTGGCTCAACACCTGTGATCTCAGCATTTGGGAGACCGAGGCGGGCGGA A G SUZ12 Ensembl:ENSG00000178691 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs762670393 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183432,RMVar_hsa_circ_82540,RMVar_hsa_circ_107506,RMVar_hsa_circ_183431,RMVar_hsa_circ_374863,RMVar_hsa_circ_376997,RMVar_hsa_circ_308402,RMVar_hsa_circ_114951,RMVar_hsa_circ_101296,RMVar_hsa_circ_183436,RMVar_hsa_circ_183434,RMVar_hsa_circ_183435,RMVar_hsa_circ_183433,RMVar_hsa_circ_8311,RMVar_hsa_circ_27202,RMVar_hsa_circ_269028,RMVar_hsa_circ_116846,RMVar_hsa_circ_49798,RMVar_hsa_circ_83378,RMVar_hsa_circ_183449,RMVar_hsa_circ_75775,RMVar_hsa_circ_183451,RMVar_hsa_circ_62157,RMVar_hsa_circ_353084,RMVar_hsa_circ_379057,RMVar_hsa_circ_112645,RMVar_hsa_circ_183452,RMVar_hsa_circ_66247,RMVar_hsa_circ_183454,RMVar_hsa_circ_93863,RMVar_hsa_circ_183456,RMVar_hsa_circ_183458,RMVar_hsa_circ_343959,RMVar_hsa_circ_352704,RMVar_hsa_circ_369532,RMVar_hsa_circ_314185,RMVar_hsa_circ_183460,RMVar_hsa_circ_121794,RMVar_hsa_circ_183459 50077 RMVar_ID_50077 Human_SNP_ID_622028134 A-to-I Human chr17 + 31990317 31990317 31990317 TATTTTTAGTAGAGATGGGGTTTCACCGTGTTAGCCAGGATGGTCTGGACCTCCTGACGTCGTGC TATTTTTAGTAGAGATGGGGTTTCACCGTGTTCGCCAGGATGGTCTGGACCTCCTGACGTCGTGC A C SUZ12 Ensembl:ENSG00000178691 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1243229989 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12964512,Human_RBP_ID_25270168 RMVar_hsa_circ_183432,RMVar_hsa_circ_82540,RMVar_hsa_circ_107506,RMVar_hsa_circ_183431,RMVar_hsa_circ_374863,RMVar_hsa_circ_376997,RMVar_hsa_circ_308402,RMVar_hsa_circ_114951,RMVar_hsa_circ_101296,RMVar_hsa_circ_183436,RMVar_hsa_circ_183434,RMVar_hsa_circ_183435,RMVar_hsa_circ_183433,RMVar_hsa_circ_8311,RMVar_hsa_circ_27202,RMVar_hsa_circ_269028,RMVar_hsa_circ_116846,RMVar_hsa_circ_49798,RMVar_hsa_circ_83378,RMVar_hsa_circ_183449,RMVar_hsa_circ_75775,RMVar_hsa_circ_183451,RMVar_hsa_circ_62157,RMVar_hsa_circ_353084,RMVar_hsa_circ_379057,RMVar_hsa_circ_112645,RMVar_hsa_circ_183452,RMVar_hsa_circ_66247,RMVar_hsa_circ_183454,RMVar_hsa_circ_93863,RMVar_hsa_circ_183456,RMVar_hsa_circ_183458,RMVar_hsa_circ_343959,RMVar_hsa_circ_352704,RMVar_hsa_circ_369532,RMVar_hsa_circ_314185,RMVar_hsa_circ_183460,RMVar_hsa_circ_121794,RMVar_hsa_circ_183459 50078 RMVar_ID_50078 Human_SNP_ID_622028324 A-to-I Human chr17 + 31990967 31990967 31990967 GATGGGATTTTGCCATCACCCATGCTGGTCTCAAACTCCTGAGCTCAAGCAATCTACCTACCTTA GATGGGATTTTGCCATCACCCATGCTGGTCTCCAACTCCTGAGCTCAAGCAATCTACCTACCTTA A C SUZ12 Ensembl:ENSG00000178691 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1038607258 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12964549 RMVar_hsa_circ_183432,RMVar_hsa_circ_82540,RMVar_hsa_circ_107506,RMVar_hsa_circ_183431,RMVar_hsa_circ_374863,RMVar_hsa_circ_376997,RMVar_hsa_circ_308402,RMVar_hsa_circ_114951,RMVar_hsa_circ_101296,RMVar_hsa_circ_183436,RMVar_hsa_circ_183434,RMVar_hsa_circ_183435,RMVar_hsa_circ_183433,RMVar_hsa_circ_8311,RMVar_hsa_circ_27202,RMVar_hsa_circ_269028,RMVar_hsa_circ_116846,RMVar_hsa_circ_49798,RMVar_hsa_circ_83378,RMVar_hsa_circ_183449,RMVar_hsa_circ_75775,RMVar_hsa_circ_183451,RMVar_hsa_circ_62157,RMVar_hsa_circ_353084,RMVar_hsa_circ_379057,RMVar_hsa_circ_112645,RMVar_hsa_circ_183452,RMVar_hsa_circ_66247,RMVar_hsa_circ_183454,RMVar_hsa_circ_93863,RMVar_hsa_circ_183456,RMVar_hsa_circ_183458,RMVar_hsa_circ_343959,RMVar_hsa_circ_352704,RMVar_hsa_circ_369532,RMVar_hsa_circ_314185,RMVar_hsa_circ_183460,RMVar_hsa_circ_121794,RMVar_hsa_circ_183459 50079 RMVar_ID_50079 Human_SNP_ID_622028627 A-to-I Human chr17 + 31992090 31992090 31992090 GAGATGAGCAGATTGCCTGAACTCAGGAGTTCAAGACCAGCCTGGGCAATATGGTGAAACCCTGT GAGATGAGCAGATTGCCTGAACTCAGGAGTTCCAGACCAGCCTGGGCAATATGGTGAAACCCTGT A C SUZ12 Ensembl:ENSG00000178691 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1388904306 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17565857 RMVar_hsa_circ_183432,RMVar_hsa_circ_82540,RMVar_hsa_circ_107506,RMVar_hsa_circ_183431,RMVar_hsa_circ_374863,RMVar_hsa_circ_376997,RMVar_hsa_circ_308402,RMVar_hsa_circ_114951,RMVar_hsa_circ_101296,RMVar_hsa_circ_183436,RMVar_hsa_circ_183434,RMVar_hsa_circ_183435,RMVar_hsa_circ_183433,RMVar_hsa_circ_8311,RMVar_hsa_circ_27202,RMVar_hsa_circ_269028,RMVar_hsa_circ_116846,RMVar_hsa_circ_49798,RMVar_hsa_circ_83378,RMVar_hsa_circ_183449,RMVar_hsa_circ_75775,RMVar_hsa_circ_183451,RMVar_hsa_circ_62157,RMVar_hsa_circ_353084,RMVar_hsa_circ_379057,RMVar_hsa_circ_112645,RMVar_hsa_circ_183452,RMVar_hsa_circ_66247,RMVar_hsa_circ_183454,RMVar_hsa_circ_93863,RMVar_hsa_circ_183456,RMVar_hsa_circ_183458,RMVar_hsa_circ_343959,RMVar_hsa_circ_352704,RMVar_hsa_circ_369532,RMVar_hsa_circ_314185,RMVar_hsa_circ_183460,RMVar_hsa_circ_121794,RMVar_hsa_circ_183459 50080 RMVar_ID_50080 Human_SNP_ID_622030288 A-to-I Human chr17 + 31998347 31998347 31998347 GCGATCCACCCACCTCGGCCTCCCAAAGTGCTAGAATTACAGGCGTAATTACCTGGCCCAAATAT GCGATCCACCCACCTCGGCCTCCCAAAGTGCTGGAATTACAGGCGTAATTACCTGGCCCAAATAT A G SUZ12 Ensembl:ENSG00000178691 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1259034979 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183432,RMVar_hsa_circ_82540,RMVar_hsa_circ_75775,RMVar_hsa_circ_183452,RMVar_hsa_circ_78444,RMVar_hsa_circ_183460,RMVar_hsa_circ_121794,RMVar_hsa_circ_183464,RMVar_hsa_circ_75876,RMVar_hsa_circ_183465 50081 RMVar_ID_50081 Human_SNP_ID_622037058 A-to-I Human chr17 + 32026655 32026655 32026655 TTCACCATGTTGGACGGGCTGGTCTCGAACTCATGATCTCAGGTGATTCATGTGCCTTGGCTTTC TTCACCATGTTGGACGGGCTGGTCTCGAACTCGTGATCTCAGGTGATTCATGTGCCTTGGCTTTC A G LRRC37B Ensembl:ENSG00000185158 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1359395026 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50949,RMVar_hsa_circ_93764,RMVar_hsa_circ_326099,RMVar_hsa_circ_183470,RMVar_hsa_circ_287847,RMVar_hsa_circ_42605,RMVar_hsa_circ_335289,RMVar_hsa_circ_183472,RMVar_hsa_circ_20303,RMVar_hsa_circ_359695,RMVar_hsa_circ_346105,RMVar_hsa_circ_316804,RMVar_hsa_circ_332521,RMVar_hsa_circ_333906,RMVar_hsa_circ_282564,RMVar_hsa_circ_183473 50082 RMVar_ID_50082 Human_SNP_ID_622067587 A-to-I Human chr17 + 32150025 32150025 32150025 CACGTGCCTCAGCCTCCCAAAGTGCTGGTATTACAGGTGTGAGCCACTGCCCCTGGCCAAAATAT CACGTGCCTCAGCCTCCCAAAGTGCTGGTATTGCAGGTGTGAGCCACTGCCCCTGGCCAAAATAT A G RHOT1 Ensembl:ENSG00000126858 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1036314513 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183480,RMVar_hsa_circ_81987,RMVar_hsa_circ_86987,RMVar_hsa_circ_183481 50083 RMVar_ID_50083 Human_SNP_ID_622068288 A-to-I Human chr17 + 32153063 32153063 32153063 GGCTCAAGTGATGTGCCTGCCTCAGCCTCCCAAAGTGCTGAGATTACAGGCGTGAGCCGCCTCAC GGCTCAAGTGATGTGCCTGCCTCAGCCTCCCAGAGTGCTGAGATTACAGGCGTGAGCCGCCTCAC A G RHOT1 Ensembl:ENSG00000126858 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1419744269 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183480,RMVar_hsa_circ_81987,RMVar_hsa_circ_86987,RMVar_hsa_circ_183481 50084 RMVar_ID_50084 Human_SNP_ID_622068370 A-to-I Human chr17 + 32153477 32153477 32153477 GGCTAGAAGTTTGAGACCAGTCTGGGGAACATAATGAGAACCTATCTGTACAAACAATTTTTAAA GGCTAGAAGTTTGAGACCAGTCTGGGGAACATCATGAGAACCTATCTGTACAAACAATTTTTAAA A C RHOT1 Ensembl:ENSG00000126858 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1009746828 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12965261 RMVar_hsa_circ_183480,RMVar_hsa_circ_81987,RMVar_hsa_circ_86987,RMVar_hsa_circ_183481 50085 RMVar_ID_50085 Human_SNP_ID_622068864 A-to-I Human chr17 + 32155421 32155421 32155421 TGACCCTGTGATCTGCCAGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGTTTGAGCCACTGCGC TGACCCTGTGATCTGCCAGCCTTGGCCTCCCAGAGTGCTGGGATTACAGGTTTGAGCCACTGCGC A G RHOT1 Ensembl:ENSG00000126858 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1314204583 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183480,RMVar_hsa_circ_81987,RMVar_hsa_circ_86987,RMVar_hsa_circ_183481 50086 RMVar_ID_50086 Human_SNP_ID_622070955 A-to-I Human chr17 + 32164604 32164604 32164604 AATACTTACTGAGGCTGAATGTGGTGGCTTACACCTGTAGTCCCAGCACTTTGGGAGGCTGAGGC AATACTTACTGAGGCTGAATGTGGTGGCTTACCCCTGTAGTCCCAGCACTTTGGGAGGCTGAGGC A C RHOT1 Ensembl:ENSG00000126858 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1346124748 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183480,RMVar_hsa_circ_81987,RMVar_hsa_circ_86987,RMVar_hsa_circ_183481 50087 RMVar_ID_50087 Human_SNP_ID_622071015 A-to-I Human chr17 + 32164901 32164901 32164901 AATAAATAAGCTGGGTGTGGTGGCTCACACCTATAATCCCAGCACTTAGGGAGGCCAAGGCAGGT AATAAATAAGCTGGGTGTGGTGGCTCACACCTGTAATCCCAGCACTTAGGGAGGCCAAGGCAGGT A G RHOT1 Ensembl:ENSG00000126858 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1253808550 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183480,RMVar_hsa_circ_81987,RMVar_hsa_circ_86987,RMVar_hsa_circ_183481 50088 RMVar_ID_50088 Human_SNP_ID_622076418 A-to-I Human chr17 + 32185444 32185444 32185444 CTCTCCTTTTTTTTGGGTCAGGGCCTTACTCTATCGCCCAGGCTAGAGTGCAGTAGCACAATCAC CTCTCCTTTTTTTTGGGTCAGGGCCTTACTCTGTCGCCCAGGCTAGAGTGCAGTAGCACAATCAC A G RHOT1 Ensembl:ENSG00000126858 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs954175334 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8449319 RMVar_hsa_circ_54370,RMVar_hsa_circ_337342,RMVar_hsa_circ_378782,RMVar_hsa_circ_349073,RMVar_hsa_circ_320435,RMVar_hsa_circ_331536,RMVar_hsa_circ_316494,RMVar_hsa_circ_307351,RMVar_hsa_circ_66712,RMVar_hsa_circ_80696,RMVar_hsa_circ_32300,RMVar_hsa_circ_183483,RMVar_hsa_circ_183485,RMVar_hsa_circ_5255,RMVar_hsa_circ_183484,RMVar_hsa_circ_72814,RMVar_hsa_circ_21058,RMVar_hsa_circ_32226,RMVar_hsa_circ_311442,RMVar_hsa_circ_322539,RMVar_hsa_circ_341407,RMVar_hsa_circ_357706,RMVar_hsa_circ_341337,RMVar_hsa_circ_321521,RMVar_hsa_circ_299590,RMVar_hsa_circ_270613,RMVar_hsa_circ_183496,RMVar_hsa_circ_183497,RMVar_hsa_circ_323733,RMVar_hsa_circ_13157,RMVar_hsa_circ_183498,RMVar_hsa_circ_81376,RMVar_hsa_circ_359368,RMVar_hsa_circ_363851,RMVar_hsa_circ_349079,RMVar_hsa_circ_317710,RMVar_hsa_circ_103548,RMVar_hsa_circ_183501,RMVar_hsa_circ_183503,RMVar_hsa_circ_183504,RMVar_hsa_circ_183505,RMVar_hsa_circ_183502,RMVar_hsa_circ_74604,RMVar_hsa_circ_41548 50089 RMVar_ID_50089 Human_SNP_ID_622086488 A-to-I Human chr17 + 32227947 32227947 32227947 CCATTGTGGATTTCATAGTCCCCCAGAGACACATGGTCCTTAAAAATTGTGTACCACTTCTTCAG CCATTGTGGATTTCATAGTCCCCCAGAGACACGTGGTCCTTAAAAATTGTGTACCACTTCTTCAG A G RHOT1 Ensembl:ENSG00000126858 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879208186 Functional Loss SNV dbSNP153 33..33 33 - - - 50090 RMVar_ID_50090 Human_SNP_ID_622086518 A-to-I Human chr17 - 32228065 32228065 32228065 TGTTTGCAACGACCGTCTGGGGAAAAAGGTCCACGTTAAATGCAACACGGATGATACCATCGGGG TGTTTGCAACGACCGTCTGGGGAAAAAGGTCCGCGTTAAATGCAACACGGATGATACCATCGGGG T C UBL5P2 Ensembl:ENSG00000266282 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879108495 Functional Loss SNV dbSNP153 33..33 33 - - - 50091 RMVar_ID_50091 Human_SNP_ID_622086521 A-to-I Human chr17 - 32228073 32228073 32228073 ATCGAGGTTGTTTGCAACGACCGTCTGGGGAAAAAGGTCCACGTTAAATGCAACACGGATGATAC ATCGAGGTTGTTTGCAACGACCGTCTGGGGAAGAAGGTCCACGTTAAATGCAACACGGATGATAC T C UBL5P2 Ensembl:ENSG00000266282 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879037419 Functional Loss SNV dbSNP153 33..33 33 - - - 50092 RMVar_ID_50092 Human_SNP_ID_622086539 A-to-I Human chr17 - 32228127 32228127 32228127 AGGCGATTTGAGCTCTAGCTAGGATGCAAGGCAATTCGAGCTCCAGCTAGGATGATCGAGGTTGT AGGCGATTTGAGCTCTAGCTAGGATGCAAGGCGATTCGAGCTCCAGCTAGGATGATCGAGGTTGT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879194755 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4418435 50093 RMVar_ID_50093 Human_SNP_ID_622100367 A-to-I Human chr17 + 32282829 32282829 32282829 TATTTTTATTACAGACGGGGTTTCACCGTGTTAGCCAGGATGATCTTGATCTCCTGACCTCGTGA TATTTTTATTACAGACGGGGTTTCACCGTGTTGGCCAGGATGATCTTGATCTCCTGACCTCGTGA A G RHBDL3 Ensembl:ENSG00000141314 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935527843 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267123 50094 RMVar_ID_50094 Human_SNP_ID_622112090 A-to-I Human chr17 - 32328632 32328631 32328632 CCCGCCTTGGCCTCCCAAAGTGCCGGGATTACAGGCGTGAGCCACTGTGCCCAGCCAGCTTTTAA CCCGCCTTGGCCTCCCAAAGTGCCGGGATTAC_GGCGTGAGCCACTGTGCCCAGCCAGCTTTTAA CT C C17orf75 Ensembl:ENSG00000108666 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1423970871 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_100998,RMVar_hsa_circ_183519 50095 RMVar_ID_50095 Human_SNP_ID_622112103 A-to-I Human chr17 - 32328665 32328665 32328665 AGGATGGTCTCGATCTTCTCACCTTGTGATCCACCCGCCTTGGCCTCCCAAAGTGCCGGGATTAC AGGATGGTCTCGATCTTCTCACCTTGTGATCCGCCCGCCTTGGCCTCCCAAAGTGCCGGGATTAC T C C17orf75 Ensembl:ENSG00000108666 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1385216622 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100998,RMVar_hsa_circ_183519 50096 RMVar_ID_50096 Human_SNP_ID_622112120 A-to-I Human chr17 - 32328701 32328701 32328701 TATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGGTCTCGATCTTCTCACCTTGTGA TATTTTTAGTAGAGACGGGGTTTCACCGTGTTGGCCAGGATGGTCTCGATCTTCTCACCTTGTGA T C C17orf75 Ensembl:ENSG00000108666 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs772698742 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100998,RMVar_hsa_circ_183519 50097 RMVar_ID_50097 Human_SNP_ID_622112132 A-to-I Human chr17 - 32328723 32328723 32328723 ACCATGCATGGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGG ACCATGCATGGCTAATTTTTTGTATTTTTAGTTGAGACGGGGTTTCACCGTGTTAGCCAGGATGG T A C17orf75 Ensembl:ENSG00000108666 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1487777863 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100998,RMVar_hsa_circ_183519 50098 RMVar_ID_50098 Human_SNP_ID_622112170 A-to-I Human chr17 - 32328881 32328881 32328881 TTTTTTGTTTTTGTTTTATTTTTTAAGACAGAATCTCGCTCTGTCACCCAGGCTGGAGTGTGGTG TTTTTTGTTTTTGTTTTATTTTTTAAGACAGAGTCTCGCTCTGTCACCCAGGCTGGAGTGTGGTG T C C17orf75 Ensembl:ENSG00000108666 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1320448130 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100998,RMVar_hsa_circ_183519 50099 RMVar_ID_50099 Human_SNP_ID_622112353 A-to-I Human chr17 - 32329481 32329481 32329481 TTTTTTTTTTTTTAATGAAATGGGGTCTCACTATGTTGCTCAGACTGGTCTTAAACTCTTGGACT TTTTTTTTTTTTTAATGAAATGGGGTCTCACTGTGTTGCTCAGACTGGTCTTAAACTCTTGGACT T C C17orf75 Ensembl:ENSG00000108666 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs988649545 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6661946 RMVar_hsa_circ_100998,RMVar_hsa_circ_183519 50100 RMVar_ID_50100 Human_SNP_ID_622112465 A-to-I Human chr17 - 32329948 32329948 32329948 GTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGGGAGGCAGAGATTGCGGTG GTCCCAGCTACTTGGGAGGCTGAGGCAGGAGACTCGCTTGAACCCGGGAGGCAGAGATTGCGGTG T G C17orf75 Ensembl:ENSG00000108666 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs780979869 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100998,RMVar_hsa_circ_183519 50101 RMVar_ID_50101 Human_SNP_ID_622117286 A-to-I Human chr17 - 32349469 32349469 32349469 TCAAGCGATTCTCCTACCTCAGCCTCCCGAGTAGCTGGGACTGCAGGCCCGCGCCACCAAGCCCG TCAAGCGATTCTCCTACCTCAGCCTCCCGAGTGGCTGGGACTGCAGGCCCGCGCCACCAAGCCCG T C C17orf75 Ensembl:ENSG00000108666 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985058682 Functional Loss SNV dbSNP153 33..33 33 - - - 50102 RMVar_ID_50102 Human_SNP_ID_622118823 A-to-I Human chr17 + 32354163 32354163 32354163 ATACCTGGCTATTTTTAAAATTTTATTTTTGTAGAGACAGGGTCTCACTATGTTGCACAGGCTGG ATACCTGGCTATTTTTAAAATTTTATTTTTGTGGAGACAGGGTCTCACTATGTTGCACAGGCTGG A G ZNF207,AC005899.5 Ensembl:ENSG00000010244,Ensembl:ENSG00000265794 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs530008975 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12965914 RMVar_hsa_circ_78022,RMVar_hsa_circ_121226,RMVar_hsa_circ_183525,RMVar_hsa_circ_183526 50103 RMVar_ID_50103 Human_SNP_ID_622118824 A-to-I Human chr17 + 32354163 32354163 32354163 ATACCTGGCTATTTTTAAAATTTTATTTTTGTAGAGACAGGGTCTCACTATGTTGCACAGGCTGG ATACCTGGCTATTTTTAAAATTTTATTTTTGTTGAGACAGGGTCTCACTATGTTGCACAGGCTGG A T ZNF207,AC005899.5 Ensembl:ENSG00000010244,Ensembl:ENSG00000265794 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs530008975 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12965914 RMVar_hsa_circ_78022,RMVar_hsa_circ_121226,RMVar_hsa_circ_183525,RMVar_hsa_circ_183526 50104 RMVar_ID_50104 Human_SNP_ID_622118825 A-to-I Human chr17 + 32354169 32354169 32354169 GGCTATTTTTAAAATTTTATTTTTGTAGAGACAGGGTCTCACTATGTTGCACAGGCTGGTCGCCC GGCTATTTTTAAAATTTTATTTTTGTAGAGACGGGGTCTCACTATGTTGCACAGGCTGGTCGCCC A G ZNF207,AC005899.5 Ensembl:ENSG00000010244,Ensembl:ENSG00000265794 Protein coding,lincRNA intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1409663458 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78022,RMVar_hsa_circ_121226,RMVar_hsa_circ_183525,RMVar_hsa_circ_183526 50105 RMVar_ID_50105 Human_SNP_ID_622119127 A-to-I Human chr17 + 32355119 32355119 32355119 TCTCAAGATGTTGATCTCAAGATGGTCTGGCTAGGTGCGGTGGCTCACGCCTGTAATCAGCACTT TCTCAAGATGTTGATCTCAAGATGGTCTGGCTGGGTGCGGTGGCTCACGCCTGTAATCAGCACTT A G ZNF207,AC005899.5 Ensembl:ENSG00000010244,Ensembl:ENSG00000265794 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054986444 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6582426,Human_RBP_ID_12965962 RMVar_hsa_circ_78022,RMVar_hsa_circ_121226,RMVar_hsa_circ_183525,RMVar_hsa_circ_183526 50106 RMVar_ID_50106 Human_SNP_ID_622119185 A-to-I Human chr17 + 32355274 32355274 32355274 AAGTTGGGCATGGTGGCACGTGCCTGTGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGGATCGCT AAGTTGGGCATGGTGGCACGTGCCTGTGTCCCTGCTACTCAGGAGGCTGAGGCAGGAGGATCGCT A T ZNF207,AC005899.5 Ensembl:ENSG00000010244,Ensembl:ENSG00000265794 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs975542842 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12965976 RMVar_hsa_circ_78022,RMVar_hsa_circ_121226,RMVar_hsa_circ_183525,RMVar_hsa_circ_183526 50107 RMVar_ID_50107 Human_SNP_ID_622121184 A-to-I Human chr17 + 32361277 32361277 32361277 TCTGAGATTCAGAATTATCTGTGACACTTTGTAGTTGTGACAAGAAGCAGAGAAACTCTGTAAAT TCTGAGATTCAGAATTATCTGTGACACTTTGTGGTTGTGACAAGAAGCAGAGAAACTCTGTAAAT A G ZNF207 Ensembl:ENSG00000010244 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs556310826 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1854769,Human_RBP_ID_9855166,Human_RBP_ID_12966139,Human_RBP_ID_22960454,Human_RBP_ID_25270859,Human_RBP_ID_26758265 RMVar_hsa_circ_36631,RMVar_hsa_circ_78022,RMVar_hsa_circ_121226,RMVar_hsa_circ_183525,RMVar_hsa_circ_94179,RMVar_hsa_circ_183526,RMVar_hsa_circ_183527,RMVar_hsa_circ_62414,RMVar_hsa_circ_328284,RMVar_hsa_circ_360330,RMVar_hsa_circ_183529,RMVar_hsa_circ_114825,RMVar_hsa_circ_183528,RMVar_hsa_circ_330513 50108 RMVar_ID_50108 Human_SNP_ID_622129097 A-to-I Human chr17 + 32388028 32388028 32388028 CGTCAGCCGCCTGAGGAGCTGAAATTACAGGCACACACCACCATGCCTGGCTAATTTTTTGTATT CGTCAGCCGCCTGAGGAGCTGAAATTACAGGCGCACACCACCATGCCTGGCTAATTTTTTGTATT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs927250529 Functional Loss SNV dbSNP153 33..33 33 - - - 50109 RMVar_ID_50109 Human_SNP_ID_622129098 A-to-I Human chr17 + 32388030 32388030 32388030 TCAGCCGCCTGAGGAGCTGAAATTACAGGCACACACCACCATGCCTGGCTAATTTTTTGTATTTT TCAGCCGCCTGAGGAGCTGAAATTACAGGCACGCACCACCATGCCTGGCTAATTTTTTGTATTTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs932265734 Functional Loss SNV dbSNP153 33..33 33 - - - 50110 RMVar_ID_50110 Human_SNP_ID_622129102 A-to-I Human chr17 + 32388048 32388048 32388048 GAAATTACAGGCACACACCACCATGCCTGGCTAATTTTTTGTATTTTTAGTAAAAATGAGATTTC GAAATTACAGGCACACACCACCATGCCTGGCTGATTTTTTGTATTTTTAGTAAAAATGAGATTTC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560110862 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12967497 50111 RMVar_ID_50111 Human_SNP_ID_622129125 A-to-I Human chr17 + 32388136 32388136 32388136 GAACTCCTGGGCTTAAGTGATCTGCCAGCCTCAGCCTCCCAAAGTTCTGGGATTATAGGTGTCAG GAACTCCTGGGCTTAAGTGATCTGCCAGCCTCGGCCTCCCAAAGTTCTGGGATTATAGGTGTCAG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1399953921 Functional Loss SNV dbSNP153 33..33 33 - - - 50112 RMVar_ID_50112 Human_SNP_ID_622129186 A-to-I Human chr17 + 32388287 32388287 32388287 GCGATCTCGGCTCACTGCAACCTACATCTCCCAGGTTCAAGCGGTTCTCCTGCCTTAGTCTCCCA GCGATCTCGGCTCACTGCAACCTACATCTCCCTGGTTCAAGCGGTTCTCCTGCCTTAGTCTCCCA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1296929434 Functional Loss SNV dbSNP153 33..33 33 - - - 50113 RMVar_ID_50113 Human_SNP_ID_622129242 A-to-I Human chr17 + 32388466 32388466 32388466 CGCCTGCCGCGGCCTCTCAAAGTGCTGGGATTACACGCATGAACCACTGCACCCGGCCTAATACA CGCCTGCCGCGGCCTCTCAAAGTGCTGGGATTGCACGCATGAACCACTGCACCCGGCCTAATACA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1461383727 Functional Loss SNV dbSNP153 33..33 33 - - - 50114 RMVar_ID_50114 Human_SNP_ID_622129427 A-to-I Human chr17 + 32389188 32389188 32389188 CATCTGGTTTGAAGACTGAAATTTCTTTGGACAGGGTCTTGCTCTGTCACCCAGGCTGGAGTGCA CATCTGGTTTGAAGACTGAAATTTCTTTGGACGGGGTCTTGCTCTGTCACCCAGGCTGGAGTGCA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1404770461 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8449508 50115 RMVar_ID_50115 Human_SNP_ID_622129441 A-to-I Human chr17 + 32389234 32389234 32389234 TCACCCAGGCTGGAGTGCAGTGGTGTGATCACAGCTCACCGCAGCCTTGACCTCCTGGACTCAAG TCACCCAGGCTGGAGTGCAGTGGTGTGATCACCGCTCACCGCAGCCTTGACCTCCTGGACTCAAG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1315843566 Functional Loss SNV dbSNP153 33..33 33 - - - 50116 RMVar_ID_50116 Human_SNP_ID_622130365 A-to-I Human chr17 + 32392248 32392248 32392248 CTCCCAGCTAATTTTTATATATATATATTATTAATAGAGACGGAGTTTCACCATTTTGGCCAGGA CTCCCAGCTAATTTTTATATATATATATTATTGATAGAGACGGAGTTTCACCATTTTGGCCAGGA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs914990202 Functional Loss SNV dbSNP153 33..33 33 - - - 50117 RMVar_ID_50117 Human_SNP_ID_622130476 A-to-I Human chr17 + 32392564 32392564 32392564 TAAAAATACAAAAATTAGCTGGGTGTGGGGGCAGGCGCCTGTAATCCCCGGTACTCTGGAGGCTG TAAAAATACAAAAATTAGCTGGGTGTGGGGGCGGGCGCCTGTAATCCCCGGTACTCTGGAGGCTG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1317185602 Functional Loss SNV dbSNP153 33..33 33 - - - 50118 RMVar_ID_50118 Human_SNP_ID_622130482 A-to-I Human chr17 + 32392574 32392574 32392574 AAAATTAGCTGGGTGTGGGGGCAGGCGCCTGTAATCCCCGGTACTCTGGAGGCTGAGCCAGGAGA AAAATTAGCTGGGTGTGGGGGCAGGCGCCTGTCATCCCCGGTACTCTGGAGGCTGAGCCAGGAGA A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1440857592 Functional Loss SNV dbSNP153 33..33 33 - - - 50119 RMVar_ID_50119 Human_SNP_ID_622130492 A-to-I Human chr17 + 32392601 32392601 32392601 CCTGTAATCCCCGGTACTCTGGAGGCTGAGCCAGGAGAATCGCTTGAACCCGGAGGCAGAGGTTG CCTGTAATCCCCGGTACTCTGGAGGCTGAGCCGGGAGAATCGCTTGAACCCGGAGGCAGAGGTTG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs912504695 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23308168 50120 RMVar_ID_50120 Human_SNP_ID_622130516 A-to-I Human chr17 + 32392651 32392651 32392651 CGGAGGCAGAGGTTGCAGTGATCCAAGATCGTACCACTGCACTCCAGCATGGGGAACAGAGCGAT CGGAGGCAGAGGTTGCAGTGATCCAAGATCGTTCCACTGCACTCCAGCATGGGGAACAGAGCGAT A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1008198379 Functional Loss SNV dbSNP153 33..33 33 - - - 50121 RMVar_ID_50121 Human_SNP_ID_622130922 A-to-I Human chr17 + 32394143 32394141 32394143 TATAAAAGAAAGCAGGCCAGGCGCGGTGGCTCACGCCTGTAATTCCAGCAGCTTGGGAGGCCGGG TATAAAAGAAAGCAGGCCAGGCGCGGTGGCT__CGCCTGTAATTCCAGCAGCTTGGGAGGCCGGG TCA T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1176739677 Functional Loss DEL dbSNP153 32..33 33 - - - 50122 RMVar_ID_50122 Human_SNP_ID_622131057 A-to-I Human chr17 + 32394597 32394597 32394597 GGGTTCAAGCGATTCCTCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGTGCACACCACCATG GGGTTCAAGCGATTCCTCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGTGCACACCACCATG A G - - Other Unknown GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1223825749 Functional Loss SNV dbSNP153 33..33 33 - - - 50123 RMVar_ID_50123 Human_SNP_ID_622131186 A-to-I Human chr17 + 32394840 32394840 32394840 TTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTGAAATGGGATTCTTGCTCTGTTGCCCAGGCTAGA TTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTGTAATGGGATTCTTGCTCTGTTGCCCAGGCTAGA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1298892051 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6583132 50124 RMVar_ID_50124 Human_SNP_ID_622131591 A-to-I Human chr17 + 32396306 32396306 32396306 AAAATTAGCTGGGTGTAGTGGCATATACCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAAGAGA AAAATTAGCTGGGTGTAGTGGCATATACCTGTTATCCCAGCTACTCGGGAGGCTGAGGCAAGAGA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1567840579 Functional Loss SNV dbSNP153 33..33 33 - - - 50125 RMVar_ID_50125 Human_SNP_ID_622132056 A-to-I Human chr17 + 32397926 32397926 32397926 TTGAGTGATCCTCCTGCCTCAGCCTCCTGAGTAACTGGGACTACAGGCATGCTGCACCACACCTG TTGAGTGATCCTCCTGCCTCAGCCTCCTGAGTGACTGGGACTACAGGCATGCTGCACCACACCTG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1437352479 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6583152 50126 RMVar_ID_50126 Human_SNP_ID_622132689 A-to-I Human chr17 + 32400491 32400491 32400491 GACTAAAGTGATCCTCTTGCCTTGGCTTCTCAAAGTGTTGGGATTATAGGCATGAACCACTGCAC GACTAAAGTGATCCTCTTGCCTTGGCTTCTCATAGTGTTGGGATTATAGGCATGAACCACTGCAC A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1308835620 Functional Loss SNV dbSNP153 33..33 33 - - - 50127 RMVar_ID_50127 Human_SNP_ID_622133789 A-to-I Human chr17 + 32404830 32404830 32404830 GGCGCGTGCTACCATGCCTGGCTAATTTTTGTATTTCTAGTAGAGACGAGTTTCACCATGTTGGC GGCGCGTGCTACCATGCCTGGCTAATTTTTGTCTTTCTAGTAGAGACGAGTTTCACCATGTTGGC A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1187521634 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12967700 50128 RMVar_ID_50128 Human_SNP_ID_622134776 A-to-I Human chr17 + 32409116 32409116 32409116 GTCGGCTCTCCCAACCCCCGCCTTCCGGGTTTAAGCAATTCTCTGCCTCAGCCTCCTGAGTAGCT GTCGGCTCTCCCAACCCCCGCCTTCCGGGTTTCAGCAATTCTCTGCCTCAGCCTCCTGAGTAGCT A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1275456922 Functional Loss SNV dbSNP153 33..33 33 - - - 50129 RMVar_ID_50129 Human_SNP_ID_622144570 A-to-I Human chr17 + 32450102 32450102 32450102 CCTGCCTCAGGCTCCCAAGTGGCTGGAACTACAGGCGCCCACCACCACCCCCGGTTAATTTCTGT CCTGCCTCAGGCTCCCAAGTGGCTGGAACTACCGGCGCCCACCACCACCCCCGGTTAATTTCTGT A C PSMD11 Ensembl:ENSG00000108671 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1051971805 Functional Loss SNV dbSNP153 33..33 33 - - - 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_183547,RMVar_hsa_circ_291310,RMVar_hsa_circ_183546,RMVar_hsa_circ_183543,RMVar_hsa_circ_183544 50130 RMVar_ID_50130 Human_SNP_ID_622144794 A-to-I Human chr17 + 32450976 32450973 32450977 ACCACATATCTACAAAAAAGATAAAAAAATTGACTGGGTGTGGTGGTGCGTGCCTGTGTCCCAGG ACCACATATCTACAAAAAAGATAAAAAAAT____TGGGTGTGGTGGTGCGTGCCTGTGTCCCAGG TTGAC T PSMD11 Ensembl:ENSG00000108671 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1243642169 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_6583258 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_183547,RMVar_hsa_circ_291310,RMVar_hsa_circ_183546,RMVar_hsa_circ_183543,RMVar_hsa_circ_183544 50131 RMVar_ID_50131 Human_SNP_ID_622146635 A-to-I Human chr17 + 32459027 32459027 32459027 TGAGGCACAAGAATCACTTGAATCCAGGAGGTAGAGGTTCCAGTGAGCCAAGATCGTGCCACTGC TGAGGCACAAGAATCACTTGAATCCAGGAGGTGGAGGTTCCAGTGAGCCAAGATCGTGCCACTGC A G PSMD11 Ensembl:ENSG00000108671 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1187053236 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6583291 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 50132 RMVar_ID_50132 Human_SNP_ID_622147336 A-to-I Human chr17 + 32461406 32461406 32461406 ACCCACAATAGCACGTTTTAAGAAACCTCTCTACTAAAAATACGAAAGTTAGCTGAGCATGGTGG ACCCACAATAGCACGTTTTAAGAAACCTCTCTGCTAAAAATACGAAAGTTAGCTGAGCATGGTGG A G PSMD11 Ensembl:ENSG00000108671 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1465272401 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 50133 RMVar_ID_50133 Human_SNP_ID_622148431 A-to-I Human chr17 + 32466027 32466023 32466027 AGAACTTTTTTTTTTCTTTGAGATGGAGTCTCACTCTGTCGTCCAGGCTGGAGTGCAGGGGTGTG AGAACTTTTTTTTTTCTTTGAGATGGAGT____CTCTGTCGTCCAGGCTGGAGTGCAGGGGTGTG TCTCA T PSMD11 Ensembl:ENSG00000108671 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1368009953 Functional Loss DEL dbSNP153 30..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_331325,RMVar_hsa_circ_304905,RMVar_hsa_circ_183545,RMVar_hsa_circ_183543,RMVar_hsa_circ_183544,RMVar_hsa_circ_183549,RMVar_hsa_circ_70569,RMVar_hsa_circ_290818,RMVar_hsa_circ_358098,RMVar_hsa_circ_104821,RMVar_hsa_circ_183550 50134 RMVar_ID_50134 Human_SNP_ID_622150236 A-to-I Human chr17 + 32473532 32473532 32473532 GAGCTCCTGACCTCAGGTGATCCGCCTGCCTCAGCCTCCCAAAGTGCTGGGATTATAGGCGTGAG GAGCTCCTGACCTCAGGTGATCCGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTATAGGCGTGAG A G PSMD11 Ensembl:ENSG00000108671 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1464835913 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_302442,RMVar_hsa_circ_320735,RMVar_hsa_circ_342095,RMVar_hsa_circ_363479,RMVar_hsa_circ_304905,RMVar_hsa_circ_183543,RMVar_hsa_circ_183544,RMVar_hsa_circ_183549,RMVar_hsa_circ_70569,RMVar_hsa_circ_358098,RMVar_hsa_circ_104821,RMVar_hsa_circ_183550,RMVar_hsa_circ_267079 50135 RMVar_ID_50135 Human_SNP_ID_622150737 A-to-I Human chr17 + 32475698 32475698 32475698 TCGGCTCACTGCATCCTCCTCCTCCCAGTTTGAAGTGATTCTCCTGTCTCAGCCTCCCGAGTAGC TCGGCTCACTGCATCCTCCTCCTCCCAGTTTGGAGTGATTCTCCTGTCTCAGCCTCCCGAGTAGC A G PSMD11 Ensembl:ENSG00000108671 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1481902786 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_320735,RMVar_hsa_circ_342095,RMVar_hsa_circ_304905,RMVar_hsa_circ_183543,RMVar_hsa_circ_127489,RMVar_hsa_circ_70569,RMVar_hsa_circ_104821,RMVar_hsa_circ_183550,RMVar_hsa_circ_357086,RMVar_hsa_circ_183553 50136 RMVar_ID_50136 Human_SNP_ID_622150767 A-to-I Human chr17 + 32475821 32475821 32475821 TTGCCATCTTGGCCAGGCTGTCCCAAACTCCTAACCTCAAGTGATCCGCCCACCTCAACCTCCAA TTGCCATCTTGGCCAGGCTGTCCCAAACTCCTGACCTCAAGTGATCCGCCCACCTCAACCTCCAA A G PSMD11 Ensembl:ENSG00000108671 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1051706817 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_320735,RMVar_hsa_circ_342095,RMVar_hsa_circ_304905,RMVar_hsa_circ_183543,RMVar_hsa_circ_127489,RMVar_hsa_circ_70569,RMVar_hsa_circ_104821,RMVar_hsa_circ_183550,RMVar_hsa_circ_357086,RMVar_hsa_circ_183553 50137 RMVar_ID_50137 Human_SNP_ID_622219865 A-to-I Human chr17 - 32764997 32764997 32764997 AAGTAGTATCTATCATAGCAGAATTGCTCTCTACTAAGACAGATATGGTTGAGAAAGCCCTTCTT AAGTAGTATCTATCATAGCAGAATTGCTCTCTGCTAAGACAGATATGGTTGAGAAAGCCCTTCTT T C MYO1D Ensembl:ENSG00000176658 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs753388708 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1803440,Human_Splice_Rec_1803486,Human_Splice_Rec_1803540,Human_Splice_Rec_1803644 RMVar_hsa_circ_85960,RMVar_hsa_circ_13448,RMVar_hsa_circ_183557,RMVar_hsa_circ_326725,RMVar_hsa_circ_121714,RMVar_hsa_circ_183568,RMVar_hsa_circ_326301,RMVar_hsa_circ_376290,RMVar_hsa_circ_287919,RMVar_hsa_circ_35271,RMVar_hsa_circ_15511,RMVar_hsa_circ_183570,RMVar_hsa_circ_183572,RMVar_hsa_circ_183571,RMVar_hsa_circ_112690,RMVar_hsa_circ_34808,RMVar_hsa_circ_1300,RMVar_hsa_circ_183578,RMVar_hsa_circ_340590,RMVar_hsa_circ_286833,RMVar_hsa_circ_101447,RMVar_hsa_circ_120524,RMVar_hsa_circ_68272,RMVar_hsa_circ_14849,RMVar_hsa_circ_183580,RMVar_hsa_circ_183582,RMVar_hsa_circ_183581,RMVar_hsa_circ_313247,RMVar_hsa_circ_183579,RMVar_hsa_circ_101783,RMVar_hsa_circ_35446,RMVar_hsa_circ_28126,RMVar_hsa_circ_280477,RMVar_hsa_circ_183588,RMVar_hsa_circ_97490,RMVar_hsa_circ_183589,RMVar_hsa_circ_183587,RMVar_hsa_circ_337211,RMVar_hsa_circ_327206,RMVar_hsa_circ_54205,RMVar_hsa_circ_183590 50138 RMVar_ID_50138 Human_SNP_ID_622502895 A-to-I Human chr17 - 33916725 33916725 33916725 CATCTCTTTGCTGTCAGTCCTTGAATCCTGAAACCTTGAAGTCATTGCAACCTCTTTGCATCCTT CATCTCTTTGCTGTCAGTCCTTGAATCCTGAAGCCTTGAAGTCATTGCAACCTCTTTGCATCCTT T C AC024610.2,ASIC2 Ensembl:ENSG00000279668,Ensembl:ENSG00000108684 lincRNA,Protein coding intron,intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs946695150 Functional Loss SNV dbSNP153 33..33 33 - - - 50139 RMVar_ID_50139 Human_SNP_ID_622533396 A-to-I Human chr17 - 34039181 34039179 34039182 AGAAAACAGTAAGAATTCTGACTTAGAGAAGAAGGAGGGAAGAATAGATGATTTATTAAGAGCCA AGAAAACAGTAAGAATTCTGACTTAGAGAAG___GAGGGAAGAATAGATGATTTATTAAGAGCCA CCTT C TLK2P1,AC004147.4,AC024610.2,ASIC2 Ensembl:ENSG00000226049,Ensembl:ENSG00000265356,Ensembl:ENSG00000279668,Ensembl:ENSG00000108684 Pseudogene,lincRNA,lincRNA,Protein coding exon,intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1304895595 Functional Loss DEL dbSNP153 32..34 33 - - - Human_RBP_ID_3547901 50140 RMVar_ID_50140 Human_SNP_ID_622787154 A-to-I Human chr17 - 35042738 35042738 35042738 TCACTGCAACCTCTGCCTCCTGGGTTCAAGCAATTATCCTGCCTTAGCCTCCTGAGTAGCTGGGA TCACTGCAACCTCTGCCTCCTGGGTTCAAGCAGTTATCCTGCCTTAGCCTCCTGAGTAGCTGGGA T C RFFL,AC004223.3 Ensembl:ENSG00000092871,Ensembl:ENSG00000267618 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs754413114 Functional Loss SNV dbSNP153 33..33 33 - - - 50141 RMVar_ID_50141 Human_SNP_ID_622787853 A-to-I Human chr17 - 35045807 35045807 35045807 GTTGGCCAGGCTGGTCTCAAACTCCTGACCTCAGGTGATCCGCCGGCTTCAGCCTCCCAAAGTGC GTTGGCCAGGCTGGTCTCAAACTCCTGACCTCTGGTGATCCGCCGGCTTCAGCCTCCCAAAGTGC T A RFFL,AC004223.3 Ensembl:ENSG00000092871,Ensembl:ENSG00000267618 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1312234359 Functional Loss SNV dbSNP153 33..33 33 - - - 50142 RMVar_ID_50142 Human_SNP_ID_622789824 A-to-I Human chr17 - 35055416 35055416 35055416 CGCCCACCTTGGCCTCCCAAAGTGCTGGGATTACAGGTGAGCCATCGCACCTGGCCTAATGCTTA CGCCCACCTTGGCCTCCCAAAGTGCTGGGATTTCAGGTGAGCCATCGCACCTGGCCTAATGCTTA T A RFFL,AC004223.3 Ensembl:ENSG00000092871,Ensembl:ENSG00000267618 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1329313660 Functional Loss SNV dbSNP153 33..33 33 - - - 50143 RMVar_ID_50143 Human_SNP_ID_622793303 A-to-I Human chr17 - 35070445 35070445 35070445 TCTAATACGATTAACTTAAACTGCTCACACCTATAATCTCAGCACTTTGGGAGGTTGAGGCAGGC TCTAATACGATTAACTTAAACTGCTCACACCTGTAATCTCAGCACTTTGGGAGGTTGAGGCAGGC T C RFFL,AC004223.3 Ensembl:ENSG00000092871,Ensembl:ENSG00000267618 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1007546723 Functional Loss SNV dbSNP153 33..33 33 - - - 50144 RMVar_ID_50144 Human_SNP_ID_622794588 A-to-I Human chr17 - 35076088 35076088 35076088 TCGAGAGGCTGAGGCAGGAGAATCCCTTGAACATGGGAGGTGGAGATTGCAGTGAGCCAAGATCA TCGAGAGGCTGAGGCAGGAGAATCCCTTGAACGTGGGAGGTGGAGATTGCAGTGAGCCAAGATCA T C RFFL,AC004223.3 Ensembl:ENSG00000092871,Ensembl:ENSG00000267618 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1339558097 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21890606,Human_RBP_ID_23308188 50145 RMVar_ID_50145 Human_SNP_ID_622796202 A-to-I Human chr17 - 35083624 35083624 35083624 GACATGCGCCACCATGTCCAGCCGATTTTTGTATTTTTTGTAGGGATGGGGTTTCACCATGTTGG GACATGCGCCACCATGTCCAGCCGATTTTTGTGTTTTTTGTAGGGATGGGGTTTCACCATGTTGG T C RFFL,AC004223.3 Ensembl:ENSG00000092871,Ensembl:ENSG00000267618 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1269765707 Functional Loss SNV dbSNP153 33..33 33 - - - 50146 RMVar_ID_50146 Human_SNP_ID_622796348 A-to-I Human chr17 - 35084153 35084153 35084153 CTCACCGCAACCTCTGCCTCCTGGGTTCAAGCAATTCTCCTGCCTCCGTCTCCCAAGTAGCTGGG CTCACCGCAACCTCTGCCTCCTGGGTTCAAGCCATTCTCCTGCCTCCGTCTCCCAAGTAGCTGGG T G RFFL,AC004223.3 Ensembl:ENSG00000092871,Ensembl:ENSG00000267618 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1408508343 Functional Loss SNV dbSNP153 33..33 33 - - - 50147 RMVar_ID_50147 Human_SNP_ID_622796708 A-to-I Human chr17 - 35085649 35085649 35085649 CAGAGGCGGGTGATTACCTGAGATCAGGAGTTAGAGACCAGCCTGACCAATATGGTGAAACCCTG CAGAGGCGGGTGATTACCTGAGATCAGGAGTTGGAGACCAGCCTGACCAATATGGTGAAACCCTG T C RFFL,AC004223.3 Ensembl:ENSG00000092871,Ensembl:ENSG00000267618 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1238175359 Functional Loss SNV dbSNP153 33..33 33 - - - 50148 RMVar_ID_50148 Human_SNP_ID_622796836 A-to-I Human chr17 - 35086314 35086314 35086314 GCCCAGCTAATTTTTGTGTTTTTGGTGGAGACAGGGTTTTGCCATGTTGCCCAGGCTGATCTCAA GCCCAGCTAATTTTTGTGTTTTTGGTGGAGACGGGGTTTTGCCATGTTGCCCAGGCTGATCTCAA T C RFFL,AC004223.3 Ensembl:ENSG00000092871,Ensembl:ENSG00000267618 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1485539163 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13220215 50149 RMVar_ID_50149 Human_SNP_ID_622796838 A-to-I Human chr17 - 35086316 35086316 35086316 ACGCCCAGCTAATTTTTGTGTTTTTGGTGGAGACAGGGTTTTGCCATGTTGCCCAGGCTGATCTC ACGCCCAGCTAATTTTTGTGTTTTTGGTGGAGGCAGGGTTTTGCCATGTTGCCCAGGCTGATCTC T C RFFL,AC004223.3 Ensembl:ENSG00000092871,Ensembl:ENSG00000267618 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1275736504 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13220215 50150 RMVar_ID_50150 Human_SNP_ID_622797054 A-to-I Human chr17 - 35087239 35087239 35087239 TTAGGTGACTCTCCCTTCTCAGCCTCCTGAGTAGCTGGGACCTCAGGCATGTGCAACCACACCCA TTAGGTGACTCTCCCTTCTCAGCCTCCTGAGTTGCTGGGACCTCAGGCATGTGCAACCACACCCA T A RFFL,AC004223.3 Ensembl:ENSG00000092871,Ensembl:ENSG00000267618 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1288288922 Functional Loss SNV dbSNP153 33..33 33 - - - 50151 RMVar_ID_50151 Human_SNP_ID_622799170 A-to-I Human chr17 - 35096804 35096804 35096804 TGCTCTGGAGTGCAGTGGCACAATCACGGCTCACTGTACCCTCTACCTCCCAAGCTCAAGTGATC TGCTCTGGAGTGCAGTGGCACAATCACGGCTCCCTGTACCCTCTACCTCCCAAGCTCAAGTGATC T G AC004223.3,RAD51D Ensembl:ENSG00000267618,Ensembl:ENSG00000185379 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1020603559 Functional Loss SNV dbSNP153 33..33 33 - - - 50152 RMVar_ID_50152 Human_SNP_ID_622799764 A-to-I Human chr17 - 35098898 35098898 35098898 TTGTGGCTGCAGTGAGCCCTGATCGCACCACTACACCCCAGCCTGGGTAACAGAGCAAGACCCTG TTGTGGCTGCAGTGAGCCCTGATCGCACCACTGCACCCCAGCCTGGGTAACAGAGCAAGACCCTG T C AC004223.3,RAD51D Ensembl:ENSG00000267618,Ensembl:ENSG00000185379 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs963722720 Functional Loss SNV dbSNP153 33..33 33 - - - 50153 RMVar_ID_50153 Human_SNP_ID_622801307 A-to-I Human chr17 - 35104433 35104433 35104433 AGGCAGAGGTTGCAGTTAGCTGAGATCATGCCACTGCACTCCAGCCTGGGTGACAGAGCAAGACT AGGCAGAGGTTGCAGTTAGCTGAGATCATGCCGCTGCACTCCAGCCTGGGTGACAGAGCAAGACT T C AC004223.3,RAD51D Ensembl:ENSG00000267618,Ensembl:ENSG00000185379 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1301082344 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183633,RMVar_hsa_circ_360587,RMVar_hsa_circ_289987,RMVar_hsa_circ_356845 50154 RMVar_ID_50154 Human_SNP_ID_622801309 A-to-I Human chr17 - 35104441 35104441 35104441 AACCGAGGAGGCAGAGGTTGCAGTTAGCTGAGATCATGCCACTGCACTCCAGCCTGGGTGACAGA AACCGAGGAGGCAGAGGTTGCAGTTAGCTGAGGTCATGCCACTGCACTCCAGCCTGGGTGACAGA T C AC004223.3,RAD51D Ensembl:ENSG00000267618,Ensembl:ENSG00000185379 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1418311849 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183633,RMVar_hsa_circ_360587,RMVar_hsa_circ_289987,RMVar_hsa_circ_356845 50155 RMVar_ID_50155 Human_SNP_ID_622802614 A-to-I Human chr17 - 35108963 35108963 35108963 ACTCGGGAGGCTGAGACAGGAGAACTGCTTGAACCTGGGAGGTGGAGGTTGCAATGAGCTGAGAT ACTCGGGAGGCTGAGACAGGAGAACTGCTTGATCCTGGGAGGTGGAGGTTGCAATGAGCTGAGAT T A AC004223.3,RAD51D Ensembl:ENSG00000267618,Ensembl:ENSG00000185379 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1033984473 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_360587 50156 RMVar_ID_50156 Human_SNP_ID_622809797 A-to-I Human chr17 - 35134582 35134582 35134582 TAGCCTGGCCAACATGGCAAAACCCTGTCTCTACTAAAAATACAAAAATTAGCCAGGCATAGTGG TAGCCTGGCCAACATGGCAAAACCCTGTCTCTCCTAAAAATACAAAAATTAGCCAGGCATAGTGG T G NLE1 Ensembl:ENSG00000073536 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs888148364 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_47655,RMVar_hsa_circ_81089,RMVar_hsa_circ_116810,RMVar_hsa_circ_183635,RMVar_hsa_circ_183636,RMVar_hsa_circ_127878,RMVar_hsa_circ_85380,RMVar_hsa_circ_183637,RMVar_hsa_circ_183638,RMVar_hsa_circ_183639 50157 RMVar_ID_50157 Human_SNP_ID_622810950 A-to-I Human chr17 - 35138372 35138372 35138372 CCCCAGAGGTTTAGTTCTATTGGGCCTGGGGTAGGGCCTGGGAATCTGCATTTCTAACAAGTTCC CCCCAGAGGTTTAGTTCTATTGGGCCTGGGGTTGGGCCTGGGAATCTGCATTTCTAACAAGTTCC T A NLE1 Ensembl:ENSG00000073536 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1247402773 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2502512 RMVar_hsa_circ_116810,RMVar_hsa_circ_183635,RMVar_hsa_circ_127878,RMVar_hsa_circ_85380,RMVar_hsa_circ_183638,RMVar_hsa_circ_183639,RMVar_hsa_circ_267634,RMVar_hsa_circ_80607,RMVar_hsa_circ_183643,RMVar_hsa_circ_76941,RMVar_hsa_circ_377452,RMVar_hsa_circ_183644,RMVar_hsa_circ_115376,RMVar_hsa_circ_183647 50158 RMVar_ID_50158 Human_SNP_ID_622811721 A-to-I Human chr17 - 35141366 35141366 35141366 AATTTTTGTATTTTTAGTGGGGACTGGGTTTCACCACGTTGGCCAGGATGGTCTCGATCTCTTGA AATTTTTGTATTTTTAGTGGGGACTGGGTTTCGCCACGTTGGCCAGGATGGTCTCGATCTCTTGA T C NLE1 Ensembl:ENSG00000073536 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1377232627 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_377452 50159 RMVar_ID_50159 Human_SNP_ID_622814412 A-to-I Human chr17 - 35151197 35151197 35151197 CGCTGAATTTAAGCATATTTGTCAGCGGAGGAAAAGAAACTAACCAGGATTCCCTCAGTAATGGC CGCTGAATTTAAGCATATTTGTCAGCGGAGGAGAAGAAACTAACCAGGATTCCCTCAGTAATGGC T C RF02543-021 RNACentral:URS000096B15F rRNA intron GSE38233 cultured B-cells - 24183664 RNA-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 50160 RMVar_ID_50160 Human_SNP_ID_622814462 A-to-I Human chr17 - 35151325 35151325 35151325 TTAGAATCCCCGCCCCGCGGTGGGGCGCGGGAAATGTGGCGTACGGAAGACCCACTCCCCGGCGC TTAGAATCCCCGCCCCGCGGTGGGGCGCGGGACATGTGGCGTACGGAAGACCCACTCCCCGGCGC T G - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-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 50161 RMVar_ID_50161 Human_SNP_ID_622842605 A-to-I Human chr17 + 35262197 35262197 35262197 GGTCAAGAGATCGAGACCATCCTGGCTAACACAGTGAAACCCTGTCTCTACTAAAAATACAAAAA GGTCAAGAGATCGAGACCATCCTGGCTAACACGGTGAAACCCTGTCTCTACTAAAAATACAAAAA A G SLFN5 Ensembl:ENSG00000166750 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1037709997 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8214 50162 RMVar_ID_50162 Human_SNP_ID_622842718 A-to-I Human chr17 + 35262621 35262621 35262621 GAGGTGGCTCACACCTGTAATCCTGGCACTTTAGGAGACCGAGGTGGGAGGATCACTTGAGCCCA GAGGTGGCTCACACCTGTAATCCTGGCACTTTGGGAGACCGAGGTGGGAGGATCACTTGAGCCCA A G SLFN5 Ensembl:ENSG00000166750 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1245312029 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8214 50163 RMVar_ID_50163 Human_SNP_ID_622842881 A-to-I Human chr17 + 35263314 35263314 35263314 CACCATGCCCGGCTAAGTTTTGTATTTTTTGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGG CACCATGCCCGGCTAAGTTTTGTATTTTTTGTGGAGATGGGGTTTCACCATGTTGGCCAGGCTGG A G SLFN5 Ensembl:ENSG00000166750 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1388185568 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8214 50164 RMVar_ID_50164 Human_SNP_ID_622842980 A-to-I Human chr17 + 35263755 35263755 35263755 TGAGGCAGGAGAATCACTTGAACCCAGGAGACAGAAGTTGCAGTGAGCCGAGATCGCACCACTGG TGAGGCAGGAGAATCACTTGAACCCAGGAGACCGAAGTTGCAGTGAGCCGAGATCGCACCACTGG A C SLFN5 Ensembl:ENSG00000166750 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs759639206 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8214 50165 RMVar_ID_50165 Human_SNP_ID_622844432 A-to-I Human chr17 + 35268052 35268052 35268052 TTCCTGGATGCTTTGCCTCCTTCATGGAATTCAGTGGATTTAATGGAAGTTCCTAGGCAACAATA TTCCTGGATGCTTTGCCTCCTTCATGGAATTCGGTGGATTTAATGGAAGTTCCTAGGCAACAATA A G SLFN5 Ensembl:ENSG00000166750 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs557554829 Functional Loss SNV dbSNP153 33..33 33 - - - 50166 RMVar_ID_50166 Human_SNP_ID_622865635 A-to-I Human chr17 - 35351507 35351507 35351507 ATCAATGAGTTTATGTTTTAACTTCTCAGCTTAGTTCTATGCATTGCTCTATAACACACCTAGTT ATCAATGAGTTTATGTTTTAACTTCTCAGCTTGGTTCTATGCATTGCTCTATAACACACCTAGTT T C SLFN11 Ensembl:ENSG00000172716 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1471667213 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1855221,Human_RBP_ID_6584429,Human_RBP_ID_8816475,Human_RBP_ID_27664099 50167 RMVar_ID_50167 Human_SNP_ID_622883262 A-to-I Human chr17 - 35421678 35421678 35421678 AAAATTAGCTGGGTGTGATGGCACGTGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGA AAAATTAGCTGGGTGTGATGGCACGTGCCTGTGGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGA T C SLFN12 Ensembl:ENSG00000172123 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1138034 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183654,RMVar_hsa_circ_297596 50168 RMVar_ID_50168 Human_SNP_ID_622907082 A-to-I Human chr17 - 35511553 35511553 35511553 TATGTGTGTGTGTGTAGAGACGAGGTCTCACCATCTTGCCCAGGCTGGTCTCTAACTCCTGGGCT TATGTGTGTGTGTGTAGAGACGAGGTCTCACCGTCTTGCCCAGGCTGGTCTCTAACTCCTGGGCT T C AC015911.11 Ensembl:ENSG00000286065 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs910375770 Functional Loss SNV dbSNP153 33..33 33 - - - 50169 RMVar_ID_50169 Human_SNP_ID_622907083 A-to-I Human chr17 - 35511553 35511553 35511553 TATGTGTGTGTGTGTAGAGACGAGGTCTCACCATCTTGCCCAGGCTGGTCTCTAACTCCTGGGCT TATGTGTGTGTGTGTAGAGACGAGGTCTCACCCTCTTGCCCAGGCTGGTCTCTAACTCCTGGGCT T G AC015911.11 Ensembl:ENSG00000286065 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs910375770 Functional Loss SNV dbSNP153 33..33 33 - - - 50170 RMVar_ID_50170 Human_SNP_ID_622921780 A-to-I Human chr17 + 35569041 35569041 35569041 AATTTTTGCGTTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGA AATTTTTGCGTTTTTAGTAGAGATGGGGTTTCTCCATGTTGGCCAGGCTGGTCTTGAACTCCTGA A T SNHG30 Ensembl:ENSG00000267321 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1402109307 Functional Loss SNV dbSNP153 33..33 33 - - - 50171 RMVar_ID_50171 Human_SNP_ID_622922820 A-to-I Human chr17 + 35572728 35572728 35572728 GTGGTGGTGCTCACCTGAGATGTCAGCTACTCAGAAGGCTGGGGTGGGAGGATTGCTTGAGCCCA GTGGTGGTGCTCACCTGAGATGTCAGCTACTCGGAAGGCTGGGGTGGGAGGATTGCTTGAGCCCA A G SNHG30 Ensembl:ENSG00000267321 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs553801780 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25273118 50172 RMVar_ID_50172 Human_SNP_ID_622924871 A-to-I Human chr17 + 35580277 35580277 35580277 AAGTTAACTAAACGTATGGCATAAGAACGCCTATAATCCCAGCACTTTGGGAGGCCGAGGCGGGT AAGTTAACTAAACGTATGGCATAAGAACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGT A G AP2B1 Ensembl:ENSG00000006125 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1339345994 Functional Loss SNV dbSNP153 33..33 33 - - - 50173 RMVar_ID_50173 Human_SNP_ID_622930047 A-to-I Human chr17 + 35599897 35599896 35599898 GTGCCACTGCACTCCAGCTTAGGCAACAGAGTAAGACTCTGTCTCAAAAATCAAAAAACAAAAAA GTGCCACTGCACTCCAGCTTAGGCAACAGAGT__GACTCTGTCTCAAAAATCAAAAAACAAAAAA TAA T AP2B1 Ensembl:ENSG00000006125 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1567777050 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_25340796 RMVar_hsa_circ_183658,RMVar_hsa_circ_311341,RMVar_hsa_circ_312410 50174 RMVar_ID_50174 Human_SNP_ID_622936960 A-to-I Human chr17 + 35628547 35628547 35628547 ATTGCTTGAGTCTGGGAGGCTGAGACTGTAGTAAGCTGTTATTGTGCCACTGCACTCCAACCTGA ATTGCTTGAGTCTGGGAGGCTGAGACTGTAGTCAGCTGTTATTGTGCCACTGCACTCCAACCTGA A C AP2B1 Ensembl:ENSG00000006125 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350901630 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12971137 RMVar_hsa_circ_13474,RMVar_hsa_circ_342450,RMVar_hsa_circ_376347,RMVar_hsa_circ_326898,RMVar_hsa_circ_183663,RMVar_hsa_circ_183662,RMVar_hsa_circ_312215,RMVar_hsa_circ_342772,RMVar_hsa_circ_374118,RMVar_hsa_circ_352305,RMVar_hsa_circ_320319,RMVar_hsa_circ_275306,RMVar_hsa_circ_272812,RMVar_hsa_circ_115586,RMVar_hsa_circ_183664,RMVar_hsa_circ_183666,RMVar_hsa_circ_183668,RMVar_hsa_circ_183667,RMVar_hsa_circ_183665,RMVar_hsa_circ_127762,RMVar_hsa_circ_375420,RMVar_hsa_circ_26731,RMVar_hsa_circ_183671,RMVar_hsa_circ_183672,RMVar_hsa_circ_183670 50175 RMVar_ID_50175 Human_SNP_ID_622952481 A-to-I Human chr17 + 35695614 35695614 35695614 AATGTATATGTGACTGCTTTCTGCCAGTGTATAACCTCCCTGTGATACTATTCTGACCAATCTTT AATGTATATGTGACTGCTTTCTGCCAGTGTATGACCTCCCTGTGATACTATTCTGACCAATCTTT A G AP2B1 Ensembl:ENSG00000006125 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1470805942 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43705,RMVar_hsa_circ_374118,RMVar_hsa_circ_183664,RMVar_hsa_circ_183665,RMVar_hsa_circ_127762,RMVar_hsa_circ_183672,RMVar_hsa_circ_2125,RMVar_hsa_circ_85483,RMVar_hsa_circ_183677,RMVar_hsa_circ_24514,RMVar_hsa_circ_183679,RMVar_hsa_circ_376258,RMVar_hsa_circ_183683,RMVar_hsa_circ_75444 50176 RMVar_ID_50176 Human_SNP_ID_622952503 A-to-I Human chr17 + 35695700 35695700 35695700 CCACTTCTAGCAGCCTACAACAGAATTACTCTATATAGTTTCAGTTGCCAGAAACAGCCAGCAAT CCACTTCTAGCAGCCTACAACAGAATTACTCTGTATAGTTTCAGTTGCCAGAAACAGCCAGCAAT A G AP2B1 Ensembl:ENSG00000006125 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1482252049 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43705,RMVar_hsa_circ_374118,RMVar_hsa_circ_183664,RMVar_hsa_circ_183665,RMVar_hsa_circ_127762,RMVar_hsa_circ_183672,RMVar_hsa_circ_2125,RMVar_hsa_circ_85483,RMVar_hsa_circ_183677,RMVar_hsa_circ_24514,RMVar_hsa_circ_183679,RMVar_hsa_circ_376258,RMVar_hsa_circ_183683,RMVar_hsa_circ_75444 50177 RMVar_ID_50177 Human_SNP_ID_622952504 A-to-I Human chr17 + 35695704 35695704 35695704 TTCTAGCAGCCTACAACAGAATTACTCTATATAGTTTCAGTTGCCAGAAACAGCCAGCAATAATT TTCTAGCAGCCTACAACAGAATTACTCTATATGGTTTCAGTTGCCAGAAACAGCCAGCAATAATT A G AP2B1 Ensembl:ENSG00000006125 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1421536179 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43705,RMVar_hsa_circ_374118,RMVar_hsa_circ_183664,RMVar_hsa_circ_183665,RMVar_hsa_circ_127762,RMVar_hsa_circ_183672,RMVar_hsa_circ_2125,RMVar_hsa_circ_85483,RMVar_hsa_circ_183677,RMVar_hsa_circ_24514,RMVar_hsa_circ_183679,RMVar_hsa_circ_376258,RMVar_hsa_circ_183683,RMVar_hsa_circ_75444 50178 RMVar_ID_50178 Human_SNP_ID_622982318 A-to-I Human chr17 + 35814096 35814096 35814096 CCTGGCTAATTTTTAAAATTTTTTGTAGAGATAGGATCTTTCTGTGTTGCCCAGGCTGGTCTTGA CCTGGCTAATTTTTAAAATTTTTTGTAGAGATGGGATCTTTCTGTGTTGCCCAGGCTGGTCTTGA A G TAF15 Ensembl:ENSG00000270647 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs558631752 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3520256,Human_RBP_ID_6585374,Human_RBP_ID_9856667,Human_RBP_ID_12972382,Human_RBP_ID_22949823,Human_RBP_ID_23168658,Human_RBP_ID_26641657 RMVar_hsa_circ_88237,RMVar_hsa_circ_183687 50179 RMVar_ID_50179 Human_SNP_ID_622982416 A-to-I Human chr17 + 35814334 35814334 35814334 ACTACAGGTGCCCACCACCACCACGTCCGGCTAATTTTCTGTATTTTTAGTAGAGACGGGATTTC ACTACAGGTGCCCACCACCACCACGTCCGGCTGATTTTCTGTATTTTTAGTAGAGACGGGATTTC A G TAF15 Ensembl:ENSG00000270647 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs888133255 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_132371,Human_RBP_ID_12972387 RMVar_hsa_circ_88237,RMVar_hsa_circ_183687 50180 RMVar_ID_50180 Human_SNP_ID_622982522 A-to-I Human chr17 + 35814682 35814682 35814682 TGAAACTAGCCTGGTCAACATGGTGAAACTCCATCTCTATTAAAAATACAAAAACTAGCCGGGCA TGAAACTAGCCTGGTCAACATGGTGAAACTCCCTCTCTATTAAAAATACAAAAACTAGCCGGGCA A C TAF15 Ensembl:ENSG00000270647 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs939757369 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23721968 RMVar_hsa_circ_88237,RMVar_hsa_circ_183687 50181 RMVar_ID_50181 Human_SNP_ID_622985584 A-to-I Human chr17 + 35825675 35825675 35825675 AGTCATTATAAATATATTTTCACTGGCCAGGCATGGTGACCCATGCCTGTAATCCCAGCACTTTG AGTCATTATAAATATATTTTCACTGGCCAGGCGTGGTGACCCATGCCTGTAATCCCAGCACTTTG A G TAF15 Ensembl:ENSG00000270647 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1568257687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_132375,Human_RBP_ID_22949926 RMVar_hsa_circ_357066,RMVar_hsa_circ_45147,RMVar_hsa_circ_362394,RMVar_hsa_circ_183695,RMVar_hsa_circ_183696,RMVar_hsa_circ_377044 50182 RMVar_ID_50182 Human_SNP_ID_622985863 A-to-I Human chr17 + 35826657 35826657 35826657 TCAGTTTACTGCAACCTCCACCTCCCAGGTTCAAACAGTTCTCCTGCCTCAGCCTCCTGAGTAGC TCAGTTTACTGCAACCTCCACCTCCCAGGTTCCAACAGTTCTCCTGCCTCAGCCTCCTGAGTAGC A C TAF15 Ensembl:ENSG00000270647 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs540177278 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25340925 RMVar_hsa_circ_357066,RMVar_hsa_circ_45147,RMVar_hsa_circ_362394,RMVar_hsa_circ_183695,RMVar_hsa_circ_183696,RMVar_hsa_circ_377044 50183 RMVar_ID_50183 Human_SNP_ID_622985914 A-to-I Human chr17 + 35826773 35826773 35826773 TTTTTTAAGTAGTGATGGGGTTTCACCGTGTTAGCTAGGATGGTCTCGATCTCCTGACCTCGTGA TTTTTTAAGTAGTGATGGGGTTTCACCGTGTTCGCTAGGATGGTCTCGATCTCCTGACCTCGTGA A C TAF15 Ensembl:ENSG00000270647 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1352349627 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_357066,RMVar_hsa_circ_45147,RMVar_hsa_circ_362394,RMVar_hsa_circ_183695,RMVar_hsa_circ_183696,RMVar_hsa_circ_377044 50184 RMVar_ID_50184 Human_SNP_ID_622985930 A-to-I Human chr17 + 35826832 35826832 35826832 TCGTGATCTGCCCGCCTTGGCCTCCCAAGATTACAGGTGTGAGCCACCACGCCTGGCTGAAGTTC TCGTGATCTGCCCGCCTTGGCCTCCCAAGATTGCAGGTGTGAGCCACCACGCCTGGCTGAAGTTC A G TAF15 Ensembl:ENSG00000270647 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1481488324 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3520326,Human_RBP_ID_9856855,Human_RBP_ID_12973061,Human_RBP_ID_17565865,Human_RBP_ID_22949942,Human_RBP_ID_25273912 RMVar_hsa_circ_357066,RMVar_hsa_circ_45147,RMVar_hsa_circ_362394,RMVar_hsa_circ_183695,RMVar_hsa_circ_183696,RMVar_hsa_circ_377044 50185 RMVar_ID_50185 Human_SNP_ID_622986045 A-to-I Human chr17 + 35827215 35827215 35827215 AAAATTAGCCGGGTGTGGTGGCGGGCTCCTGTAGTCCCAGCTACCCTGGAGGCTGAGGGAGGAGA AAAATTAGCCGGGTGTGGTGGCGGGCTCCTGTGGTCCCAGCTACCCTGGAGGCTGAGGGAGGAGA A G TAF15 Ensembl:ENSG00000270647 Protein coding intron GSE38233;GSE100210;GSE107867;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;ASD brains,cerebellum;ASD brains,temporal_cortex;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,30559470,30559470,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs964158578 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_132378,Human_RBP_ID_4420477,Human_RBP_ID_12973085 RMVar_hsa_circ_357066,RMVar_hsa_circ_45147,RMVar_hsa_circ_362394,RMVar_hsa_circ_183695,RMVar_hsa_circ_183696,RMVar_hsa_circ_377044 50186 RMVar_ID_50186 Human_SNP_ID_622986046 A-to-I Human chr17 + 35827221 35827221 35827221 AGCCGGGTGTGGTGGCGGGCTCCTGTAGTCCCAGCTACCCTGGAGGCTGAGGGAGGAGAATGGTG AGCCGGGTGTGGTGGCGGGCTCCTGTAGTCCCGGCTACCCTGGAGGCTGAGGGAGGAGAATGGTG A G TAF15 Ensembl:ENSG00000270647 Protein coding intron GSE38233;GSE100210;GSE107867;GSE107867;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank;ASD brains,frontal_cortex;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,30559470,30559470,31158229 RNA-Seq:(High) rs1435257306 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_132378,Human_RBP_ID_12973085 RMVar_hsa_circ_357066,RMVar_hsa_circ_45147,RMVar_hsa_circ_362394,RMVar_hsa_circ_183695,RMVar_hsa_circ_183696,RMVar_hsa_circ_377044 50187 RMVar_ID_50187 Human_SNP_ID_622986060 A-to-I Human chr17 + 35827261 35827261 35827261 TGGAGGCTGAGGGAGGAGAATGGTGTGAACCCAGGAGGCGGAGCTTGCAGTGAGCTGAGATCGCA TGGAGGCTGAGGGAGGAGAATGGTGTGAACCCGGGAGGCGGAGCTTGCAGTGAGCTGAGATCGCA A G TAF15 Ensembl:ENSG00000270647 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,31158229,31158229 RNA-Seq:(High) rs377315332 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_357066,RMVar_hsa_circ_45147,RMVar_hsa_circ_362394,RMVar_hsa_circ_183695,RMVar_hsa_circ_183696,RMVar_hsa_circ_377044 50188 RMVar_ID_50188 Human_SNP_ID_622986169 A-to-I Human chr17 + 35827583 35827583 35827583 AAAAAATTAGCTGGACACGATGGTGGGTGCCTATAATCCCAGCTACTCGGGAGGCTGAGACAGGA AAAAAATTAGCTGGACACGATGGTGGGTGCCTGTAATCCCAGCTACTCGGGAGGCTGAGACAGGA A G TAF15 Ensembl:ENSG00000270647 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs545787135 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25273941 RMVar_hsa_circ_357066,RMVar_hsa_circ_45147,RMVar_hsa_circ_362394,RMVar_hsa_circ_183695,RMVar_hsa_circ_183696,RMVar_hsa_circ_377044 50189 RMVar_ID_50189 Human_SNP_ID_622988810 A-to-I Human chr17 + 35836810 35836810 35836810 ATTACTCTTTTTTTTTTTTGAGACAGAATCTCACTGTTTCACCAGGCTGGAGTGCAGTGGCGCGA ATTACTCTTTTTTTTTTTTGAGACAGAATCTCCCTGTTTCACCAGGCTGGAGTGCAGTGGCGCGA A C TAF15 Ensembl:ENSG00000270647 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1361765848 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_357066,RMVar_hsa_circ_362394,RMVar_hsa_circ_183695,RMVar_hsa_circ_183697,RMVar_hsa_circ_183696,RMVar_hsa_circ_377044,RMVar_hsa_circ_347346,RMVar_hsa_circ_68222,RMVar_hsa_circ_295269,RMVar_hsa_circ_183698,RMVar_hsa_circ_332059 50190 RMVar_ID_50190 Human_SNP_ID_622988924 A-to-I Human chr17 + 35837205 35837203 35837205 AGGGTCTTGCTTCATTCCATCCAGGCTGGAGTACAGTGGCATAATCATGGGTCACTGCAGCCTCA AGGGTCTTGCTTCATTCCATCCAGGCTGGAG__CAGTGGCATAATCATGGGTCACTGCAGCCTCA GTA G TAF15 Ensembl:ENSG00000270647 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1471650008 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_12973648 RMVar_hsa_circ_357066,RMVar_hsa_circ_362394,RMVar_hsa_circ_183695,RMVar_hsa_circ_183697,RMVar_hsa_circ_183696,RMVar_hsa_circ_377044,RMVar_hsa_circ_347346,RMVar_hsa_circ_68222,RMVar_hsa_circ_295269,RMVar_hsa_circ_183698,RMVar_hsa_circ_332059 50191 RMVar_ID_50191 Human_SNP_ID_622989067 A-to-I Human chr17 + 35837670 35837670 35837670 TAACACGATGAAACCCTGTCTCTACTGAAAATACAAGAAATTAGATGGGCGTGGTGGCATGCGCC TAACACGATGAAACCCTGTCTCTACTGAAAATGCAAGAAATTAGATGGGCGTGGTGGCATGCGCC A G TAF15 Ensembl:ENSG00000270647 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs564674202 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_357066,RMVar_hsa_circ_362394,RMVar_hsa_circ_183695,RMVar_hsa_circ_183697,RMVar_hsa_circ_183696,RMVar_hsa_circ_377044,RMVar_hsa_circ_347346,RMVar_hsa_circ_68222,RMVar_hsa_circ_295269,RMVar_hsa_circ_183698,RMVar_hsa_circ_332059 50192 RMVar_ID_50192 Human_SNP_ID_622989070 A-to-I Human chr17 + 35837680 35837680 35837680 AAACCCTGTCTCTACTGAAAATACAAGAAATTAGATGGGCGTGGTGGCATGCGCCTGTAGTCCCA AAACCCTGTCTCTACTGAAAATACAAGAAATTTGATGGGCGTGGTGGCATGCGCCTGTAGTCCCA A T TAF15 Ensembl:ENSG00000270647 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1300710926 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_357066,RMVar_hsa_circ_362394,RMVar_hsa_circ_183695,RMVar_hsa_circ_183697,RMVar_hsa_circ_183696,RMVar_hsa_circ_377044,RMVar_hsa_circ_347346,RMVar_hsa_circ_68222,RMVar_hsa_circ_295269,RMVar_hsa_circ_183698,RMVar_hsa_circ_332059 50193 RMVar_ID_50193 Human_SNP_ID_622989088 A-to-I Human chr17 + 35837716 35837716 35837716 GGGCGTGGTGGCATGCGCCTGTAGTCCCAGCTACTTGGGCGGCTGAGGCAGGAGAGTGATGTGAA GGGCGTGGTGGCATGCGCCTGTAGTCCCAGCTGCTTGGGCGGCTGAGGCAGGAGAGTGATGTGAA A G TAF15 Ensembl:ENSG00000270647 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1286815175 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_357066,RMVar_hsa_circ_362394,RMVar_hsa_circ_183695,RMVar_hsa_circ_183697,RMVar_hsa_circ_183696,RMVar_hsa_circ_377044,RMVar_hsa_circ_347346,RMVar_hsa_circ_68222,RMVar_hsa_circ_295269,RMVar_hsa_circ_183698,RMVar_hsa_circ_332059 50194 RMVar_ID_50194 Human_SNP_ID_622989449 A-to-I Human chr17 + 35839008 35839008 35839008 GAAATTTAGGCCAGGTGGCATTGCTTATGCCTATAATCCCAGTGCTTTGGGAGGCTGAGGCAGGA GAAATTTAGGCCAGGTGGCATTGCTTATGCCTGTAATCCCAGTGCTTTGGGAGGCTGAGGCAGGA A G TAF15 Ensembl:ENSG00000270647 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs186228584 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12973690,Human_RBP_ID_23308206 RMVar_hsa_circ_362394,RMVar_hsa_circ_183695,RMVar_hsa_circ_50226,RMVar_hsa_circ_68222 50195 RMVar_ID_50195 Human_SNP_ID_622989913 A-to-I Human chr17 + 35840369 35840363 35840369 CGCCTCCTGGGTTCACGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGTACATG CGCCTCCTGGGTTCACGCCATTCTCCT______GCCTCCCGAGTAGCTGGGACTACAGGTACATG TGCCTCA T TAF15 Ensembl:ENSG00000270647 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1178637572 Functional Loss DEL dbSNP153 28..33 33 - - - RMVar_hsa_circ_362394,RMVar_hsa_circ_183695,RMVar_hsa_circ_50226,RMVar_hsa_circ_68222 50196 RMVar_ID_50196 Human_SNP_ID_623015317 A-to-I Human chr17 - 35939517 35939513 35939517 TCCATGATAAATAAAAATCTATAAAATAATAAACAAGAGAAAAGAGATTGGAAACAGCCAGGTTG TCCATGATAAATAAAAATCTATAAAATAATAA____GAGAAAAGAGATTGGAAACAGCCAGGTTG CTTGT C LYZL6 Ensembl:ENSG00000275722 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs931012601 Functional Loss DEL dbSNP153 33..36 33 - - - Human_Splice_Rec_1806390 50197 RMVar_ID_50197 Human_SNP_ID_623138948 A-to-I Human chr17 - 36497086 36497086 36497086 ACCTCAAGTGGTCTGCCTGCCTTGCCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGTGC ACCTCAAGTGGTCTGCCTGCCTTGCCCTCCCATAGTGCTGGGATTACAGGTGTGAGCCACCGTGC T A MYO19 Ensembl:ENSG00000278259 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1403232580 Functional Loss SNV dbSNP153 33..33 33 - - - 50198 RMVar_ID_50198 Human_SNP_ID_623139015 A-to-I Human chr17 - 36497301 36497301 36497301 TTTTTTTTTTTTTCATGTTATTTAATTTTTTGAGACGGAGTCTCACTCTGTCGCCCAGGATGGAA TTTTTTTTTTTTTCATGTTATTTAATTTTTTGTGACGGAGTCTCACTCTGTCGCCCAGGATGGAA T A MYO19 Ensembl:ENSG00000278259 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1173075675 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12976371 50199 RMVar_ID_50199 Human_SNP_ID_623145032 A-to-I Human chr17 - 36516508 36516508 36516508 AAATTAGCCAGGCGTGGTGGCGTGCGCCTGTAATCCTAGCTACTTGGGAGGCTGAGGCAGGAGAA AAATTAGCCAGGCGTGGTGGCGTGCGCCTGTAGTCCTAGCTACTTGGGAGGCTGAGGCAGGAGAA T C MYO19 Ensembl:ENSG00000278259 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs918599597 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_337596 50200 RMVar_ID_50200 Human_SNP_ID_623145074 A-to-I Human chr17 - 36516607 36516607 36516607 ATCCCACTTTGGGAGGCCAAGGTGGGCAGATTACGAGGTCAGGAGCTCAAGACCAGACTCACCAA ATCCCACTTTGGGAGGCCAAGGTGGGCAGATTTCGAGGTCAGGAGCTCAAGACCAGACTCACCAA T A MYO19 Ensembl:ENSG00000278259 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1026216057 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9857216,Human_RBP_ID_12976798,Human_RBP_ID_25341076 RMVar_hsa_circ_337596 50201 RMVar_ID_50201 Human_SNP_ID_623145079 A-to-I Human chr17 - 36516620 36516620 36516620 GCTCACACCTGTAATCCCACTTTGGGAGGCCAAGGTGGGCAGATTACGAGGTCAGGAGCTCAAGA GCTCACACCTGTAATCCCACTTTGGGAGGCCACGGTGGGCAGATTACGAGGTCAGGAGCTCAAGA T G MYO19 Ensembl:ENSG00000278259 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984117611 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12976801 RMVar_hsa_circ_337596 50202 RMVar_ID_50202 Human_SNP_ID_623145408 A-to-I Human chr17 - 36517867 36517867 36517867 CAAGGCTGGTTTTGAACTGCTGAACTCAGGCAATCCACCCACCTCAGCCTCCCAAAGTGCTGGGA CAAGGCTGGTTTTGAACTGCTGAACTCAGGCAGTCCACCCACCTCAGCCTCCCAAAGTGCTGGGA T C MYO19 Ensembl:ENSG00000278259 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1044440111 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12976841 RMVar_hsa_circ_337596 50203 RMVar_ID_50203 Human_SNP_ID_623145409 A-to-I Human chr17 - 36517868 36517868 36517868 TCAAGGCTGGTTTTGAACTGCTGAACTCAGGCAATCCACCCACCTCAGCCTCCCAAAGTGCTGGG TCAAGGCTGGTTTTGAACTGCTGAACTCAGGCGATCCACCCACCTCAGCCTCCCAAAGTGCTGGG T C MYO19 Ensembl:ENSG00000278259 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs887119851 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12976841 RMVar_hsa_circ_337596 50204 RMVar_ID_50204 Human_SNP_ID_623145415 A-to-I Human chr17 - 36517897 36517897 36517897 TTAGTAGAGACAGGGTTTCACCATGTTGGTCAAGGCTGGTTTTGAACTGCTGAACTCAGGCAATC TTAGTAGAGACAGGGTTTCACCATGTTGGTCAGGGCTGGTTTTGAACTGCTGAACTCAGGCAATC T C MYO19 Ensembl:ENSG00000278259 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1421439427 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12976841 RMVar_hsa_circ_337596 50205 RMVar_ID_50205 Human_SNP_ID_623145417 A-to-I Human chr17 - 36517907 36517907 36517907 TTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGGTCAAGGCTGGTTTTGAACTGCTGAAC TTTTGTATTTTTAGTAGAGACAGGGTTTCACCGTGTTGGTCAAGGCTGGTTTTGAACTGCTGAAC T C MYO19 Ensembl:ENSG00000278259 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs906071044 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_337596 50206 RMVar_ID_50206 Human_SNP_ID_623145426 A-to-I Human chr17 - 36517981 36517981 36517981 GGTTCAAGCGATTCTCCTGCCTCAGTCTCCCTAGTAGCTGGAATTACAGGTGGATGCCATGACAC GGTTCAAGCGATTCTCCTGCCTCAGTCTCCCTCGTAGCTGGAATTACAGGTGGATGCCATGACAC T G MYO19 Ensembl:ENSG00000278259 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1340828732 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12976843,Human_RBP_ID_25274679 RMVar_hsa_circ_337596 50207 RMVar_ID_50207 Human_SNP_ID_623145432 A-to-I Human chr17 - 36518007 36518007 36518007 CAGCTCACTGCAACCTGCGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGTCTCCCTAGTAGCT CAGCTCACTGCAACCTGCGCCTCCCGGGTTCAGGCGATTCTCCTGCCTCAGTCTCCCTAGTAGCT T C MYO19 Ensembl:ENSG00000278259 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs746974584 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_337596 50208 RMVar_ID_50208 Human_SNP_ID_623145804 A-to-I Human chr17 - 36518779 36518779 36518779 ATCTATCTATCTGTCTATCTATCTATCTCACTATGCCTGGGTTTAAATCTACCATCTTATTTTTT ATCTATCTATCTGTCTATCTATCTATCTCACTGTGCCTGGGTTTAAATCTACCATCTTATTTTTT T C MYO19 Ensembl:ENSG00000278259 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1332247282 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2503145,Human_RBP_ID_6586797,Human_RBP_ID_12976875 RMVar_hsa_circ_337596 50209 RMVar_ID_50209 Human_SNP_ID_623146019 A-to-I Human chr17 - 36519562 36519562 36519562 CTTATATGATAGAATGGAATCATTAAAATGCCAAATTTAATCAAAGGCAATAAGAAAAAAGGGAA CTTATATGATAGAATGGAATCATTAAAATGCCTAATTTAATCAAAGGCAATAAGAAAAAAGGGAA T A MYO19 Ensembl:ENSG00000278259 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1308724472 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12976894,Human_RBP_ID_27664380 RMVar_hsa_circ_337596 50210 RMVar_ID_50210 Human_SNP_ID_623146027 A-to-I Human chr17 - 36519606 36519606 36519606 TCTCTTTAGAAGATAATCACTATAAGGCACAAATGGTAACAATGCTTATATGATAGAATGGAATC TCTCTTTAGAAGATAATCACTATAAGGCACAAGTGGTAACAATGCTTATATGATAGAATGGAATC T C MYO19 Ensembl:ENSG00000278259 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037389256 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_49916,Human_RBP_ID_2503151,Human_RBP_ID_6586802,Human_RBP_ID_9857251 RMVar_hsa_circ_337596 50211 RMVar_ID_50211 Human_SNP_ID_623148880 A-to-I Human chr17 - 36529275 36529275 36529275 CATGCCTCTAGTCCCAATTACTCAGGAAGCTGAGGCAGAAGGATCACTTGAGCTCAGGAGTTGGA CATGCCTCTAGTCCCAATTACTCAGGAAGCTGGGGCAGAAGGATCACTTGAGCTCAGGAGTTGGA T C MYO19 Ensembl:ENSG00000278259 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1188883580 Functional Loss SNV dbSNP153 33..33 33 - - - 50212 RMVar_ID_50212 Human_SNP_ID_623148881 A-to-I Human chr17 - 36529280 36529280 36529280 TGACTCATGCCTCTAGTCCCAATTACTCAGGAAGCTGAGGCAGAAGGATCACTTGAGCTCAGGAG TGACTCATGCCTCTAGTCCCAATTACTCAGGATGCTGAGGCAGAAGGATCACTTGAGCTCAGGAG T A MYO19 Ensembl:ENSG00000278259 Protein coding intron GSE47997;GSE38233;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;cultured B-cells;Bronchiolar epithelium,BERP35T4 cell line - 23474544,24183664,31158229 RNA-Seq:(High) rs1022637711 Functional Loss SNV dbSNP153 33..33 33 - - - 50213 RMVar_ID_50213 Human_SNP_ID_623148882 A-to-I Human chr17 - 36529284 36529284 36529284 AGGGTGACTCATGCCTCTAGTCCCAATTACTCAGGAAGCTGAGGCAGAAGGATCACTTGAGCTCA AGGGTGACTCATGCCTCTAGTCCCAATTACTCCGGAAGCTGAGGCAGAAGGATCACTTGAGCTCA T G MYO19 Ensembl:ENSG00000278259 Protein coding intron GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs969747732 Functional Loss SNV dbSNP153 33..33 33 - - - 50214 RMVar_ID_50214 Human_SNP_ID_623149086 A-to-I Human chr17 - 36530018 36530018 36530018 TAGAGACAAGGTCTTGCTCTGTTGGCCAGGCTAGAGTGCAGCGGTACAATCATAACTCATTGCAG TAGAGACAAGGTCTTGCTCTGTTGGCCAGGCTCGAGTGCAGCGGTACAATCATAACTCATTGCAG T G MYO19 Ensembl:ENSG00000278259 Protein coding intron GSE47997;GSE38233;GSE100210;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,24183664,29129909,31158229 RNA-Seq:(High) rs377044368 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2503207,Human_RBP_ID_12977422 50215 RMVar_ID_50215 Human_SNP_ID_623149340 A-to-I Human chr17 - 36530753 36530753 36530753 AGCCAGGTATGGTGGTGCATGCCTGTGATCCCAGTTACTTGGGTGGCTGAGGCATGAGAATCACT AGCCAGGTATGGTGGTGCATGCCTGTGATCCCGGTTACTTGGGTGGCTGAGGCATGAGAATCACT T C MYO19 Ensembl:ENSG00000278259 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs190665384 Functional Loss SNV dbSNP153 33..33 33 - - - 50216 RMVar_ID_50216 Human_SNP_ID_623149404 A-to-I Human chr17 - 36531000 36531000 36531000 AAACTCCTGACCTCAAGTGATCCGTCTGCCTCAGCCTCCCAAAGTGCTTTTACAGGGGTGAGCCA AAACTCCTGACCTCAAGTGATCCGTCTGCCTCCGCCTCCCAAAGTGCTTTTACAGGGGTGAGCCA T G MYO19 Ensembl:ENSG00000278259 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs551708974 Functional Loss SNV dbSNP153 33..33 33 - - - 50217 RMVar_ID_50217 Human_SNP_ID_623149412 A-to-I Human chr17 - 36531017 36531017 36531017 TAGACAAGGCTGGTCTCAAACTCCTGACCTCAAGTGATCCGTCTGCCTCAGCCTCCCAAAGTGCT TAGACAAGGCTGGTCTCAAACTCCTGACCTCAGGTGATCCGTCTGCCTCAGCCTCCCAAAGTGCT T C MYO19 Ensembl:ENSG00000278259 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1255557763 Functional Loss SNV dbSNP153 33..33 33 - - - 50218 RMVar_ID_50218 Human_SNP_ID_623149506 A-to-I Human chr17 - 36531313 36531313 36531313 TTGGCTCACTGCAATCTCTGCCTCCCAGGTTCATGCTATTCTCCTGCCTCAGCCTCCCGAGTAGT TTGGCTCACTGCAATCTCTGCCTCCCAGGTTCGTGCTATTCTCCTGCCTCAGCCTCCCGAGTAGT T C MYO19 Ensembl:ENSG00000278259 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1413600012 Functional Loss SNV dbSNP153 33..33 33 - - - 50219 RMVar_ID_50219 Human_SNP_ID_623149508 A-to-I Human chr17 - 36531319 36531319 36531319 TTGATCTTGGCTCACTGCAATCTCTGCCTCCCAGGTTCATGCTATTCTCCTGCCTCAGCCTCCCG TTGATCTTGGCTCACTGCAATCTCTGCCTCCCGGGTTCATGCTATTCTCCTGCCTCAGCCTCCCG T C MYO19 Ensembl:ENSG00000278259 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1020630336 Functional Loss SNV dbSNP153 33..33 33 - - - 50220 RMVar_ID_50220 Human_SNP_ID_623153137 A-to-I Human chr17 - 36542982 36542982 36542982 GACGGGGGCGGCGGCTAACACCTGTAATCCCAAGACTTTGGGAGGCCAAGGCGGGCGGGTCACTT GACGGGGGCGGCGGCTAACACCTGTAATCCCACGACTTTGGGAGGCCAAGGCGGGCGGGTCACTT T G MYO19 Ensembl:ENSG00000278259 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1407648231 Functional Loss SNV dbSNP153 33..33 33 - - - 50221 RMVar_ID_50221 Human_SNP_ID_623155276 A-to-I Human chr17 + 36549415 36549410 36549415 TTAGAAGAGATGGGGGTTTCCCTATGTTGGCCAGGCTGGTCTTGAACTCCTGACCTCAGGTCATC TTAGAAGAGATGGGGGTTTCCCTATGTT_____GGCTGGTCTTGAACTCCTGACCTCAGGTCATC TGGCCA T GGNBP2 Ensembl:ENSG00000278311 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1231553192 Functional Loss DEL dbSNP153 29..33 33 - - - RMVar_hsa_circ_65606 50222 RMVar_ID_50222 Human_SNP_ID_623155898 A-to-I Human chr17 + 36551770 36551770 36551770 AGAATTGCTTGAACCTGGGAGGCAGAGGCTGCAGTGAGTCGAGATTGAGCTACTGCACTCCAGCC AGAATTGCTTGAACCTGGGAGGCAGAGGCTGCGGTGAGTCGAGATTGAGCTACTGCACTCCAGCC A G GGNBP2 Ensembl:ENSG00000278311 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1168517383 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_65606 50223 RMVar_ID_50223 Human_SNP_ID_623158308 A-to-I Human chr17 + 36560210 36560210 36560210 GAACTCCTGGCCTCAAGTGATCCTCTTACCTCAGCCTTCCAAAGTGCTGGGATTATAGGCATGAG GAACTCCTGGCCTCAAGTGATCCTCTTACCTCCGCCTTCCAAAGTGCTGGGATTATAGGCATGAG A C GGNBP2 Ensembl:ENSG00000278311 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1021874681 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 50224 RMVar_ID_50224 Human_SNP_ID_623160422 A-to-I Human chr17 + 36568109 36568109 36568109 CGCCACACCCAGCTAATTTTTGTATTTCTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGATGG CGCCACACCCAGCTAATTTTTGTATTTCTAGTGGAGATGGGGTTTCACCATGTTGGCCAGGATGG A G GGNBP2 Ensembl:ENSG00000278311 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1474654710 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55157,RMVar_hsa_circ_70115,RMVar_hsa_circ_305037,RMVar_hsa_circ_41902,RMVar_hsa_circ_347232,RMVar_hsa_circ_367384 50225 RMVar_ID_50225 Human_SNP_ID_623160448 A-to-I Human chr17 + 36568192 36568192 36568192 GTGATCCACCAACCTCGGCCTCCCAAAGTGCTAGGATTACAGGCATGAGCCACTGCGCTTGGCCA GTGATCCACCAACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGCGCTTGGCCA A G GGNBP2 Ensembl:ENSG00000278311 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs962559369 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55157,RMVar_hsa_circ_70115,RMVar_hsa_circ_305037,RMVar_hsa_circ_41902,RMVar_hsa_circ_347232,RMVar_hsa_circ_367384 50226 RMVar_ID_50226 Human_SNP_ID_623160718 A-to-I Human chr17 + 36569256 36569256 36569256 CAACGTGGCGAAACCCCGTGTCTACTAAAAATAAAAAAATTAGCCAGGCATGGTGGCACGCACGT CAACGTGGCGAAACCCCGTGTCTACTAAAAATTAAAAAATTAGCCAGGCATGGTGGCACGCACGT A T GGNBP2 Ensembl:ENSG00000278311 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs564589556 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55157,RMVar_hsa_circ_70115,RMVar_hsa_circ_305037,RMVar_hsa_circ_41902,RMVar_hsa_circ_347232,RMVar_hsa_circ_367384 50227 RMVar_ID_50227 Human_SNP_ID_623161134 A-to-I Human chr17 + 36570855 36570855 36570855 CCAGCCTGGCCAACATGGTGAAACCCCTCTCTACTGAAAATACATAAATTAGCCAGGCATGGTGG CCAGCCTGGCCAACATGGTGAAACCCCTCTCTGCTGAAAATACATAAATTAGCCAGGCATGGTGG A G GGNBP2 Ensembl:ENSG00000278311 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1203743037 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55157,RMVar_hsa_circ_70115,RMVar_hsa_circ_305037,RMVar_hsa_circ_41902,RMVar_hsa_circ_347232,RMVar_hsa_circ_367384 50228 RMVar_ID_50228 Human_SNP_ID_623162673 A-to-I Human chr17 + 36575844 36575844 36575844 AATATTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGATCTCGAACTCCTGA AATATTTGTATTTTTAGTAGAGACGGGGTTTCGCCATGTTGGCCAGGCTGATCTCGAACTCCTGA A G GGNBP2 Ensembl:ENSG00000278311 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1055456046 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55157,RMVar_hsa_circ_70115,RMVar_hsa_circ_305037,RMVar_hsa_circ_41902,RMVar_hsa_circ_347232,RMVar_hsa_circ_367384 50229 RMVar_ID_50229 Human_SNP_ID_623166111 A-to-I Human chr17 + 36587887 36587887 36587887 CCAGCCTGGCGACAGAGTGAGACTTTGTCTCAAAAAAAACCTGAGTAGAACCATTGACCATTGTT CCAGCCTGGCGACAGAGTGAGACTTTGTCTCAGAAAAAACCTGAGTAGAACCATTGACCATTGTT A G GGNBP2 Ensembl:ENSG00000278311 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1393330696 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12978190 RMVar_hsa_circ_99221,RMVar_hsa_circ_88163,RMVar_hsa_circ_183722,RMVar_hsa_circ_183725 50230 RMVar_ID_50230 Human_SNP_ID_623166335 A-to-I Human chr17 + 36588618 36588618 36588618 TAGTTTTAATATTTATTTATTTTTTTTTTTTGAGGAGTCTCGCTCTGTCGCCCAGGCTAGATAGA TAGTTTTAATATTTATTTATTTTTTTTTTTTGTGGAGTCTCGCTCTGTCGCCCAGGCTAGATAGA A T GGNBP2 Ensembl:ENSG00000278311 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1244215360 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2503275,Human_RBP_ID_6587155,Human_RBP_ID_12978218 RMVar_hsa_circ_99221,RMVar_hsa_circ_88163,RMVar_hsa_circ_183722,RMVar_hsa_circ_183725 50231 RMVar_ID_50231 Human_SNP_ID_623166358 A-to-I Human chr17 + 36588692 36588692 36588692 CACGATCTTGGCTCACTGTAGCCTCTGCCTCCAAGGTTCAAGTGATTCTCCTGCCTCAGCCTCCC CACGATCTTGGCTCACTGTAGCCTCTGCCTCCGAGGTTCAAGTGATTCTCCTGCCTCAGCCTCCC A G GGNBP2 Ensembl:ENSG00000278311 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs577498996 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9857470 RMVar_hsa_circ_99221,RMVar_hsa_circ_88163,RMVar_hsa_circ_183722,RMVar_hsa_circ_183725 50232 RMVar_ID_50232 Human_SNP_ID_623166359 A-to-I Human chr17 + 36588692 36588692 36588692 CACGATCTTGGCTCACTGTAGCCTCTGCCTCCAAGGTTCAAGTGATTCTCCTGCCTCAGCCTCCC CACGATCTTGGCTCACTGTAGCCTCTGCCTCCTAGGTTCAAGTGATTCTCCTGCCTCAGCCTCCC A T GGNBP2 Ensembl:ENSG00000278311 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs577498996 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9857470 RMVar_hsa_circ_99221,RMVar_hsa_circ_88163,RMVar_hsa_circ_183722,RMVar_hsa_circ_183725 50233 RMVar_ID_50233 Human_SNP_ID_623170460 A-to-I Human chr17 + 36604547 36604547 36604547 AGATGGGGTCAGCTGGGCACAATGGCTCACGCATGTAATCCCAGCACTTTGGGAGGCTGAGGCAG AGATGGGGTCAGCTGGGCACAATGGCTCACGCGTGTAATCCCAGCACTTTGGGAGGCTGAGGCAG A G MRM1 Ensembl:ENSG00000278619 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs572554713 Functional Loss SNV dbSNP153 33..33 33 - - - 50234 RMVar_ID_50234 Human_SNP_ID_623171123 A-to-I Human chr17 + 36607019 36607019 36607019 TGACTGCAGCCTCTGCCTCCCGAGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGA TGACTGCAGCCTCTGCCTCCCGAGTTCAAGCGGTTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGA A G MRM1 Ensembl:ENSG00000278619 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs568968790 Functional Loss SNV dbSNP153 33..33 33 - - - 50235 RMVar_ID_50235 Human_SNP_ID_623171146 A-to-I Human chr17 + 36607148 36607148 36607148 GTTGTTCAGACTGGTCTCGAACTCCCAACCTCAGGTGATCCCCCTGCCTTGGCCTCCCAAAGTGC GTTGTTCAGACTGGTCTCGAACTCCCAACCTCGGGTGATCCCCCTGCCTTGGCCTCCCAAAGTGC A G MRM1 Ensembl:ENSG00000278619 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1374777458 Functional Loss SNV dbSNP153 33..33 33 - - - 50236 RMVar_ID_50236 Human_SNP_ID_623259962 A-to-I Human chr17 + 36954350 36954350 36954350 GCAATCCTCCCACCTTTGCTTCCCAAAGTGCTAGGATTACAGATGTGACCTACTGAGCCTGGCCC GCAATCCTCCCACCTTTGCTTCCCAAAGTGCTGGGATTACAGATGTGACCTACTGAGCCTGGCCC A G AATF Ensembl:ENSG00000275700 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1405413818 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13228165 RMVar_hsa_circ_51709 50237 RMVar_ID_50237 Human_SNP_ID_623269778 A-to-I Human chr17 + 36996383 36996383 36996383 CTGAGACCAGGAGGTCGAAGCTACGGTGAGCCAAGATCGCATCACTACACTCCAGCCTGGGCGAC CTGAGACCAGGAGGTCGAAGCTACGGTGAGCCCAGATCGCATCACTACACTCCAGCCTGGGCGAC A C AATF Ensembl:ENSG00000275700 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs891427553 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38948,RMVar_hsa_circ_280468,RMVar_hsa_circ_69044 50238 RMVar_ID_50238 Human_SNP_ID_623269779 A-to-I Human chr17 + 36996383 36996383 36996383 CTGAGACCAGGAGGTCGAAGCTACGGTGAGCCAAGATCGCATCACTACACTCCAGCCTGGGCGAC CTGAGACCAGGAGGTCGAAGCTACGGTGAGCCGAGATCGCATCACTACACTCCAGCCTGGGCGAC A G AATF Ensembl:ENSG00000275700 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs891427553 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38948,RMVar_hsa_circ_280468,RMVar_hsa_circ_69044 50239 RMVar_ID_50239 Human_SNP_ID_623271470 A-to-I Human chr17 + 37003624 37003624 37003624 AAGTAGCTGGAACTAAAGGCGTGCACCACCACACCCGGCTGGTTTTTGTATTTTTAGTAGAGATG AAGTAGCTGGAACTAAAGGCGTGCACCACCACCCCCGGCTGGTTTTTGTATTTTTAGTAGAGATG A C AATF Ensembl:ENSG00000275700 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1286060108 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_38948,RMVar_hsa_circ_280468,RMVar_hsa_circ_69044 50240 RMVar_ID_50240 Human_SNP_ID_623291230 A-to-I Human chr17 - 37085797 37085797 37085797 GGACAAGCCACAGTTCTGAGCCTTAACCCTGTAGTTTGCACACAAGAACGAGCTCCACCTCCCCT GGACAAGCCACAGTTCTGAGCCTTAACCCTGTGGTTTGCACACAAGAACGAGCTCCACCTCCCCT T C ACACA Ensembl:ENSG00000278540 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1373702948 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8816747,Human_RBP_ID_12981363,Human_RBP_ID_18438806 Human_miRNA_ID_275784,Human_miRNA_ID_2181433,Human_miRNA_ID_2183537 RMVar_hsa_circ_93575,RMVar_hsa_circ_183737 50241 RMVar_ID_50241 Human_SNP_ID_623291453 A-to-I Human chr17 - 37086707 37086707 37086707 TAAAATCTACTACAAGCTCCATAGGAACTCAAAGATGAGGGCAAAACTGTGAGCCAAGAAGCAGA TAAAATCTACTACAAGCTCCATAGGAACTCAACGATGAGGGCAAAACTGTGAGCCAAGAAGCAGA T G ACACA Ensembl:ENSG00000278540 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1428798198 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26457371 Human_miRNA_ID_2286408,Human_miRNA_ID_2289407 RMVar_hsa_circ_93575,RMVar_hsa_circ_183737 50242 RMVar_ID_50242 Human_SNP_ID_623306600 A-to-I Human chr17 - 37154301 37154301 37154301 TTTTAATGTAGAGGGTTTTTGTTTTTAGAGACAGGGTTTTACTCTGTTGCCTAGGCTGGGATGCA TTTTAATGTAGAGGGTTTTTGTTTTTAGAGACGGGGTTTTACTCTGTTGCCTAGGCTGGGATGCA T C ACACA Ensembl:ENSG00000278540 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1313342659 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6588020,Human_RBP_ID_12981799 RMVar_hsa_circ_26159,RMVar_hsa_circ_32188,RMVar_hsa_circ_74902,RMVar_hsa_circ_306981,RMVar_hsa_circ_326218,RMVar_hsa_circ_314445,RMVar_hsa_circ_303283,RMVar_hsa_circ_57998,RMVar_hsa_circ_14902,RMVar_hsa_circ_23530 50243 RMVar_ID_50243 Human_SNP_ID_623307802 A-to-I Human chr17 - 37159421 37159421 37159421 GGCCAGGAGTTCGAGATCAGCCTGGCTAACATAGCGAAATACCATCTCTACTAAAATATAAAAAA GGCCAGGAGTTCGAGATCAGCCTGGCTAACATGGCGAAATACCATCTCTACTAAAATATAAAAAA T C ACACA Ensembl:ENSG00000278540 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1411084845 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26159,RMVar_hsa_circ_13233,RMVar_hsa_circ_32188,RMVar_hsa_circ_74902,RMVar_hsa_circ_306981,RMVar_hsa_circ_314445,RMVar_hsa_circ_303283,RMVar_hsa_circ_57998,RMVar_hsa_circ_14902,RMVar_hsa_circ_23530,RMVar_hsa_circ_348001,RMVar_hsa_circ_14033 50244 RMVar_ID_50244 Human_SNP_ID_623307803 A-to-I Human chr17 - 37159423 37159423 37159423 GAGGCCAGGAGTTCGAGATCAGCCTGGCTAACATAGCGAAATACCATCTCTACTAAAATATAAAA GAGGCCAGGAGTTCGAGATCAGCCTGGCTAACGTAGCGAAATACCATCTCTACTAAAATATAAAA T C ACACA Ensembl:ENSG00000278540 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005935209 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26159,RMVar_hsa_circ_13233,RMVar_hsa_circ_32188,RMVar_hsa_circ_74902,RMVar_hsa_circ_306981,RMVar_hsa_circ_314445,RMVar_hsa_circ_303283,RMVar_hsa_circ_57998,RMVar_hsa_circ_14902,RMVar_hsa_circ_23530,RMVar_hsa_circ_348001,RMVar_hsa_circ_14033 50245 RMVar_ID_50245 Human_SNP_ID_623312866 A-to-I Human chr17 - 37181330 37181330 37181330 CTGCAGATCATGTTTCAGGCATATGGAGACAAACAGGGACCACTGCATGGAATGTTAATCAATAC CTGCAGATCATGTTTCAGGCATATGGAGACAAGCAGGGACCACTGCATGGAATGTTAATCAATAC T C ACACA Ensembl:ENSG00000278540 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256981292 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9288996,Human_RBP_ID_12982046 Human_Splice_Rec_1807562,Human_Splice_Rec_1807666,Human_Splice_Rec_1807774,Human_Splice_Rec_1807818,Human_Splice_Rec_1807924,Human_Splice_Rec_1808000 Human_miRNA_ID_2880136,Human_miRNA_ID_2880137,Human_miRNA_ID_2897136,Human_miRNA_ID_2897137 RMVar_hsa_circ_13233,RMVar_hsa_circ_32188,RMVar_hsa_circ_74902,RMVar_hsa_circ_314445,RMVar_hsa_circ_303283,RMVar_hsa_circ_57998,RMVar_hsa_circ_14902,RMVar_hsa_circ_23530,RMVar_hsa_circ_14033,RMVar_hsa_circ_13985,RMVar_hsa_circ_14873,RMVar_hsa_circ_57607,RMVar_hsa_circ_310006,RMVar_hsa_circ_286932,RMVar_hsa_circ_270327,RMVar_hsa_circ_183742,RMVar_hsa_circ_5405 50246 RMVar_ID_50246 Human_SNP_ID_623317803 A-to-I Human chr17 - 37203135 37203135 37203135 CAATATGGTGAAACCCCGTCTCTACTGAAAATACAAAAATTAGCCAGGTGTGGTGGCGGGCGCCT CAATATGGTGAAACCCCGTCTCTACTGAAAATCCAAAAATTAGCCAGGTGTGGTGGCGGGCGCCT T G ACACA Ensembl:ENSG00000278540 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232802926 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4860,RMVar_hsa_circ_13233,RMVar_hsa_circ_32188,RMVar_hsa_circ_74902,RMVar_hsa_circ_57998,RMVar_hsa_circ_23530,RMVar_hsa_circ_5405,RMVar_hsa_circ_28738,RMVar_hsa_circ_36355,RMVar_hsa_circ_25975,RMVar_hsa_circ_5983,RMVar_hsa_circ_66184 50247 RMVar_ID_50247 Human_SNP_ID_623319978 A-to-I Human chr17 - 37213115 37213115 37213115 TGGATTTTGGAGATGTTGCCTGGGCTGGTCTTAAACTCCTGGGCTCAAGTGATCCACCCACCTCA TGGATTTTGGAGATGTTGCCTGGGCTGGTCTTTAACTCCTGGGCTCAAGTGATCCACCCACCTCA T A ACACA Ensembl:ENSG00000278540 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1171679353 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5648849,Human_RBP_ID_23758863 RMVar_hsa_circ_4860,RMVar_hsa_circ_13233,RMVar_hsa_circ_57998,RMVar_hsa_circ_5405,RMVar_hsa_circ_28738,RMVar_hsa_circ_36355,RMVar_hsa_circ_25975,RMVar_hsa_circ_5983 50248 RMVar_ID_50248 Human_SNP_ID_623338642 A-to-I Human chr17 - 37293679 37293679 37293679 AAACTAGCTGGGCATGGTGGTGTGTGCCTGTAATCCCAGCTACTGGGGGGCTGAGGCTGGAGAAT AAACTAGCTGGGCATGGTGGTGTGTGCCTGTAGTCCCAGCTACTGGGGGGCTGAGGCTGGAGAAT T C ACACA Ensembl:ENSG00000278540 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1212028427 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_322370,RMVar_hsa_circ_17513,RMVar_hsa_circ_30214,RMVar_hsa_circ_29460 50249 RMVar_ID_50249 Human_SNP_ID_623339447 A-to-I Human chr17 - 37297225 37297225 37297225 GTTGGTCAGACTGGTCTCGAACTCTCGACCTCAGGTGATATGCCCGCCTTGGCCTCTCAAAGTGC GTTGGTCAGACTGGTCTCGAACTCTCGACCTCTGGTGATATGCCCGCCTTGGCCTCTCAAAGTGC T A ACACA Ensembl:ENSG00000278540 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1399151117 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_322370,RMVar_hsa_circ_17513,RMVar_hsa_circ_30214,RMVar_hsa_circ_29460 50250 RMVar_ID_50250 Human_SNP_ID_623339496 A-to-I Human chr17 - 37297410 37297410 37297410 CGAGACAGAGTTTCACTTTTGTCGCCCATGCTAGAGTGTGATGGCGCGATCTTGGCTCACCACAA CGAGACAGAGTTTCACTTTTGTCGCCCATGCTGGAGTGTGATGGCGCGATCTTGGCTCACCACAA T C ACACA Ensembl:ENSG00000278540 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs996002164 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_322370,RMVar_hsa_circ_17513,RMVar_hsa_circ_30214,RMVar_hsa_circ_29460 50251 RMVar_ID_50251 Human_SNP_ID_623364010 A-to-I Human chr17 - 37396114 37396114 37396114 GCTGGCCTCGAACTCCTGACCCCAGATGATCCACCCGACTCGGCCCTCCAAAGTGCTGGGATTAC GCTGGCCTCGAACTCCTGACCCCAGATGATCCGCCCGACTCGGCCCTCCAAAGTGCTGGGATTAC T C ACACA Ensembl:ENSG00000278540 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs531995348 Functional Loss SNV dbSNP153 33..33 33 - - - 50252 RMVar_ID_50252 Human_SNP_ID_623368245 A-to-I Human chr17 + 37411497 37411497 37411497 CAGGCTGGGGTACAGTGGCATGATGTTGGCTCACTGCAACTTCTGCCTCCCGGCTTTAAACGGTT CAGGCTGGGGTACAGTGGCATGATGTTGGCTCGCTGCAACTTCTGCCTCCCGGCTTTAAACGGTT A G TADA2A Ensembl:ENSG00000276234 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1354486156 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19545,RMVar_hsa_circ_306468,RMVar_hsa_circ_314366,RMVar_hsa_circ_349306,RMVar_hsa_circ_57152 50253 RMVar_ID_50253 Human_SNP_ID_623369842 A-to-I Human chr17 + 37417634 37417634 37417634 TCAGCTCACTGCCATCTCTGCCTCCTAGGTTCAAGTGATTCTCATGCCACAGCCTCCCGAGTAGC TCAGCTCACTGCCATCTCTGCCTCCTAGGTTCGAGTGATTCTCATGCCACAGCCTCCCGAGTAGC A G TADA2A Ensembl:ENSG00000276234 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs995567195 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19545,RMVar_hsa_circ_306468,RMVar_hsa_circ_314366,RMVar_hsa_circ_349306,RMVar_hsa_circ_57152 50254 RMVar_ID_50254 Human_SNP_ID_623371572 A-to-I Human chr17 + 37424009 37424009 37424009 TAACCTCATGATCCATCTGCCTCAGCCTCCCAAAGTTCTGGGATTACAGGCGTGAGCCACCGCAC TAACCTCATGATCCATCTGCCTCAGCCTCCCAGAGTTCTGGGATTACAGGCGTGAGCCACCGCAC A G TADA2A Ensembl:ENSG00000276234 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs912127572 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_306468,RMVar_hsa_circ_314366,RMVar_hsa_circ_349306,RMVar_hsa_circ_57152,RMVar_hsa_circ_18670,RMVar_hsa_circ_292727,RMVar_hsa_circ_323033,RMVar_hsa_circ_26784 50255 RMVar_ID_50255 Human_SNP_ID_623372028 A-to-I Human chr17 + 37425672 37425672 37425672 GATTTCAGAGAGTTTTTTTATTTTTTTGAGACAGGGTTTCACTGTGTCCTCTAGGCTGGAGTGCA GATTTCAGAGAGTTTTTTTATTTTTTTGAGACTGGGTTTCACTGTGTCCTCTAGGCTGGAGTGCA A T TADA2A Ensembl:ENSG00000276234 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1470973780 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_306468,RMVar_hsa_circ_314366,RMVar_hsa_circ_349306,RMVar_hsa_circ_57152,RMVar_hsa_circ_18670,RMVar_hsa_circ_292727,RMVar_hsa_circ_323033,RMVar_hsa_circ_26784 50256 RMVar_ID_50256 Human_SNP_ID_623376125 A-to-I Human chr17 + 37441023 37441023 37441023 AGGCCAAGGCAGGAGAATCACTTGAACCGGGTAGGCGGAGATTGCAGTGAGCCAAGATCACATCA AGGCCAAGGCAGGAGAATCACTTGAACCGGGTGGGCGGAGATTGCAGTGAGCCAAGATCACATCA A G TADA2A Ensembl:ENSG00000276234 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1228543405 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_306468,RMVar_hsa_circ_314366,RMVar_hsa_circ_57152,RMVar_hsa_circ_5968,RMVar_hsa_circ_32288,RMVar_hsa_circ_323033,RMVar_hsa_circ_280652,RMVar_hsa_circ_291754,RMVar_hsa_circ_328434,RMVar_hsa_circ_362322,RMVar_hsa_circ_48701,RMVar_hsa_circ_290105,RMVar_hsa_circ_183758,RMVar_hsa_circ_294316,RMVar_hsa_circ_304723,RMVar_hsa_circ_290275,RMVar_hsa_circ_277223,RMVar_hsa_circ_183761,RMVar_hsa_circ_30324,RMVar_hsa_circ_55726,RMVar_hsa_circ_16779,RMVar_hsa_circ_183763 50257 RMVar_ID_50257 Human_SNP_ID_623376656 A-to-I Human chr17 + 37443077 37443077 37443077 CCAACTACTTGGCAGGCTGATATGGGAGGATCACTTGAGCCTGGGAGGTTAAGGCTGTAGCGAGT CCAACTACTTGGCAGGCTGATATGGGAGGATCGCTTGAGCCTGGGAGGTTAAGGCTGTAGCGAGT A G TADA2A Ensembl:ENSG00000276234 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1411071760 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_306468,RMVar_hsa_circ_314366,RMVar_hsa_circ_5968,RMVar_hsa_circ_32288,RMVar_hsa_circ_323033,RMVar_hsa_circ_280652,RMVar_hsa_circ_328434,RMVar_hsa_circ_362322,RMVar_hsa_circ_48701,RMVar_hsa_circ_290105,RMVar_hsa_circ_304723,RMVar_hsa_circ_290275,RMVar_hsa_circ_277223,RMVar_hsa_circ_30324,RMVar_hsa_circ_55726,RMVar_hsa_circ_297436 50258 RMVar_ID_50258 Human_SNP_ID_623378744 A-to-I Human chr17 + 37451458 37451458 37451458 CTCCCACCTCAGCCTCCCAAGTAGCTGGGACTACAGGCACATACCACCATGTCTGGCTATATTTT CTCCCACCTCAGCCTCCCAAGTAGCTGGGACTGCAGGCACATACCACCATGTCTGGCTATATTTT A G TADA2A Ensembl:ENSG00000276234 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1390547967 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_314366,RMVar_hsa_circ_5968,RMVar_hsa_circ_32288,RMVar_hsa_circ_328434,RMVar_hsa_circ_362322,RMVar_hsa_circ_48701,RMVar_hsa_circ_304723,RMVar_hsa_circ_290275,RMVar_hsa_circ_277223,RMVar_hsa_circ_55726,RMVar_hsa_circ_348283 50259 RMVar_ID_50259 Human_SNP_ID_623378757 A-to-I Human chr17 + 37451511 37451511 37451511 TGGCTATATTTTTGGTACATTTTTGTAGAGACAGGGTTTCACTATGTTGCCCAGGCTGGTCTCGA TGGCTATATTTTTGGTACATTTTTGTAGAGACCGGGTTTCACTATGTTGCCCAGGCTGGTCTCGA A C TADA2A Ensembl:ENSG00000276234 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1383648089 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_314366,RMVar_hsa_circ_5968,RMVar_hsa_circ_32288,RMVar_hsa_circ_328434,RMVar_hsa_circ_362322,RMVar_hsa_circ_48701,RMVar_hsa_circ_304723,RMVar_hsa_circ_290275,RMVar_hsa_circ_277223,RMVar_hsa_circ_55726,RMVar_hsa_circ_348283 50260 RMVar_ID_50260 Human_SNP_ID_623381014 A-to-I Human chr17 + 37459950 37459950 37459950 TAGCTGGGGGTGGTGGTGCATGCCTGTAGTCCAAGCTACTCGGGAGGCTGAGGCAGGAGAATTGC TAGCTGGGGGTGGTGGTGCATGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATTGC A C TADA2A Ensembl:ENSG00000276234 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1437400289 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_314366,RMVar_hsa_circ_5968,RMVar_hsa_circ_328434,RMVar_hsa_circ_362322,RMVar_hsa_circ_48701,RMVar_hsa_circ_304723,RMVar_hsa_circ_290275,RMVar_hsa_circ_277223,RMVar_hsa_circ_55726,RMVar_hsa_circ_348283,RMVar_hsa_circ_334789 50261 RMVar_ID_50261 Human_SNP_ID_623385306 A-to-I Human chr17 + 37477484 37477484 37477484 TTTAAGCTGACAACTTTTTTTTTTTTTTTTTGAGACAGAGTTTGCTCTTGTCCTCCAGGCTGGAG TTTAAGCTGACAACTTTTTTTTTTTTTTTTTGGGACAGAGTTTGCTCTTGTCCTCCAGGCTGGAG A G TADA2A Ensembl:ENSG00000276234 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs3209140 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18695868 Human_Splice_Rec_1808273,Human_Splice_Rec_1808419 50262 RMVar_ID_50262 Human_SNP_ID_623385307 A-to-I Human chr17 + 37477484 37477484 37477484 TTTAAGCTGACAACTTTTTTTTTTTTTTTTTGAGACAGAGTTTGCTCTTGTCCTCCAGGCTGGAG TTTAAGCTGACAACTTTTTTTTTTTTTTTTTGTGACAGAGTTTGCTCTTGTCCTCCAGGCTGGAG A T TADA2A Ensembl:ENSG00000276234 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs3209140 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18695868 Human_Splice_Rec_1808273,Human_Splice_Rec_1808419 50263 RMVar_ID_50263 Human_SNP_ID_623385367 A-to-I Human chr17 + 37477729 37477729 37477729 CAGGTGATCTGCCCGCCTCAGCCTCCCAAAGTACTAGGATTACAGGCGTGAGCCATCGCGCCCGG CAGGTGATCTGCCCGCCTCAGCCTCCCAAAGTGCTAGGATTACAGGCGTGAGCCATCGCGCCCGG A G TADA2A Ensembl:ENSG00000276234 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1233763443 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23168882 50264 RMVar_ID_50264 Human_SNP_ID_623385421 A-to-I Human chr17 + 37477888 37477888 37477888 GCTCACCTGTAATCCCAGCACTTTGGGAGGCTAAGGTGGGCGGATCACGAAGTCAGGAGTTCAAG GCTCACCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGCGGATCACGAAGTCAGGAGTTCAAG A G TADA2A Ensembl:ENSG00000276234 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs777689775 Functional Loss SNV dbSNP153 33..33 33 - - - 50265 RMVar_ID_50265 Human_SNP_ID_623385463 A-to-I Human chr17 + 37478038 37478038 37478038 TACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAACACAGGAGGCAGAGGTTGCAGCGAGCTGAGA TACTCAGGAGGCTGAGGCAGGAGAATTGCTTGGACACAGGAGGCAGAGGTTGCAGCGAGCTGAGA A G TADA2A Ensembl:ENSG00000276234 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1134568 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1808420 50266 RMVar_ID_50266 Human_SNP_ID_623385482 A-to-I Human chr17 + 37478101 37478101 37478101 GATCACGCCACTGTGCTCCAGCCTGGGCAACAAAGTGAGACTCTGTCTCAAAAAAAAAAAAACAA GATCACGCCACTGTGCTCCAGCCTGGGCAACACAGTGAGACTCTGTCTCAAAAAAAAAAAAACAA A C TADA2A Ensembl:ENSG00000276234 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1359673786 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1808274,Human_Splice_Rec_1808420 50267 RMVar_ID_50267 Human_SNP_ID_623387004 A-to-I Human chr17 + 37484326 37484326 37484326 ACAATCTCGGCTCACTGTAACCTATGCCTCCCAGATTCAAGCAATTCTCCTGTCTCAGCCTTCTG ACAATCTCGGCTCACTGTAACCTATGCCTCCCCGATTCAAGCAATTCTCCTGTCTCAGCCTTCTG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs374013272 Functional Loss SNV dbSNP153 33..33 33 - - - 50268 RMVar_ID_50268 Human_SNP_ID_623391730 A-to-I Human chr17 + 37502285 37502285 37502285 CTCCCTGCCCCTTTGACCTTCTGGACTCAAGCAATCCTTCTGCCTCTGCCTGCCATGTAGCTGGG CTCCCTGCCCCTTTGACCTTCTGGACTCAAGCCATCCTTCTGCCTCTGCCTGCCATGTAGCTGGG A C DUSP14 Ensembl:ENSG00000276023 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs531726787 Functional Loss SNV dbSNP153 33..33 33 - - - 50269 RMVar_ID_50269 Human_SNP_ID_623391766 A-to-I Human chr17 + 37502386 37502386 37502386 TTTTTTTTTTTGTAGAGAGAGAGTCTTCTCACATTGCTTCAGTTGGTCTTGAACTCCTGGGCTCA TTTTTTTTTTTGTAGAGAGAGAGTCTTCTCACGTTGCTTCAGTTGGTCTTGAACTCCTGGGCTCA A G DUSP14 Ensembl:ENSG00000276023 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1391228492 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12986169 50270 RMVar_ID_50270 Human_SNP_ID_623395775 A-to-I Human chr17 - 37515570 37515570 37515570 CCTGTAATCCGAGCTACTCGGGAGGCTGAGGCAGGAGAATTGCTTGAACCAGAGAGGCGGAGGTT CCTGTAATCCGAGCTACTCGGGAGGCTGAGGCGGGAGAATTGCTTGAACCAGAGAGGCGGAGGTT T C SYNRG Ensembl:ENSG00000275066 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1471064296 Functional Loss SNV dbSNP153 33..33 33 - - - 50271 RMVar_ID_50271 Human_SNP_ID_623396078 A-to-I Human chr17 - 37517003 37517003 37517003 TCCATGTTGGCCAGGCTTGAACTCCGGACCTCAGGCGATCCGCCCGCCTCAGCCTCCCAAAGTAC TCCATGTTGGCCAGGCTTGAACTCCGGACCTCGGGCGATCCGCCCGCCTCAGCCTCCCAAAGTAC T C SYNRG Ensembl:ENSG00000275066 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1133543 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4421742,Human_RBP_ID_6588899,Human_RBP_ID_12986292,Human_RBP_ID_18695891 50272 RMVar_ID_50272 Human_SNP_ID_623396087 A-to-I Human chr17 - 37517042 37517042 37517042 GCCCAGCTAATTTTGTATTTTTAGTAGAGGCAAGGTTTCTCCATGTTGGCCAGGCTTGAACTCCG GCCCAGCTAATTTTGTATTTTTAGTAGAGGCAGGGTTTCTCCATGTTGGCCAGGCTTGAACTCCG T C SYNRG Ensembl:ENSG00000275066 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs557614217 Functional Loss SNV dbSNP153 33..33 33 - - - 50273 RMVar_ID_50273 Human_SNP_ID_623396089 A-to-I Human chr17 - 37517049 37517049 37517049 CCACCACGCCCAGCTAATTTTGTATTTTTAGTAGAGGCAAGGTTTCTCCATGTTGGCCAGGCTTG CCACCACGCCCAGCTAATTTTGTATTTTTAGTGGAGGCAAGGTTTCTCCATGTTGGCCAGGCTTG T C SYNRG Ensembl:ENSG00000275066 Protein coding 3'UTR GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs1442813805 Functional Loss SNV dbSNP153 33..33 33 - - - 50274 RMVar_ID_50274 Human_SNP_ID_623396122 A-to-I Human chr17 - 37517157 37517157 37517157 CAGGCTTGAGTGCAATGGCACAATCTCAGCTCAGTGCAACCTCCGCCTCCCGGGTTCAAGCGATT CAGGCTTGAGTGCAATGGCACAATCTCAGCTCCGTGCAACCTCCGCCTCCCGGGTTCAAGCGATT T G SYNRG Ensembl:ENSG00000275066 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs541608420 Functional Loss SNV dbSNP153 33..33 33 - - - 50275 RMVar_ID_50275 Human_SNP_ID_623396123 A-to-I Human chr17 - 37517162 37517162 37517162 TTGCCCAGGCTTGAGTGCAATGGCACAATCTCAGCTCAGTGCAACCTCCGCCTCCCGGGTTCAAG TTGCCCAGGCTTGAGTGCAATGGCACAATCTCGGCTCAGTGCAACCTCCGCCTCCCGGGTTCAAG T C SYNRG Ensembl:ENSG00000275066 Protein coding 3'UTR GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1363486581 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_134725,Human_RBP_ID_25277331 50276 RMVar_ID_50276 Human_SNP_ID_623396125 A-to-I Human chr17 - 37517167 37517167 37517167 TCTTGTTGCCCAGGCTTGAGTGCAATGGCACAATCTCAGCTCAGTGCAACCTCCGCCTCCCGGGT TCTTGTTGCCCAGGCTTGAGTGCAATGGCACATTCTCAGCTCAGTGCAACCTCCGCCTCCCGGGT T A SYNRG Ensembl:ENSG00000275066 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs931014871 Functional Loss SNV dbSNP153 33..33 33 - - - 50277 RMVar_ID_50277 Human_SNP_ID_623396126 A-to-I Human chr17 - 37517167 37517167 37517167 TCTTGTTGCCCAGGCTTGAGTGCAATGGCACAATCTCAGCTCAGTGCAACCTCCGCCTCCCGGGT TCTTGTTGCCCAGGCTTGAGTGCAATGGCACAGTCTCAGCTCAGTGCAACCTCCGCCTCCCGGGT T C SYNRG Ensembl:ENSG00000275066 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs931014871 Functional Loss SNV dbSNP153 33..33 33 - - - 50278 RMVar_ID_50278 Human_SNP_ID_623396128 A-to-I Human chr17 - 37517175 37517175 37517175 AGTTTCACTCTTGTTGCCCAGGCTTGAGTGCAATGGCACAATCTCAGCTCAGTGCAACCTCCGCC AGTTTCACTCTTGTTGCCCAGGCTTGAGTGCAGTGGCACAATCTCAGCTCAGTGCAACCTCCGCC T C SYNRG Ensembl:ENSG00000275066 Protein coding 3'UTR GSE47997;GSE107867 K562 cells&HepG2 cells;ASD brains,temporal_cortex - 23474544,30559470 RNA-Seq:(High) rs1346440577 Functional Loss SNV dbSNP153 33..33 33 - - - 50279 RMVar_ID_50279 Human_SNP_ID_623396134 A-to-I Human chr17 - 37517201 37517201 37517201 AAATTCTTTGTTTTTTTTTGAGATGGAGTTTCACTCTTGTTGCCCAGGCTTGAGTGCAATGGCAC AAATTCTTTGTTTTTTTTTGAGATGGAGTTTCGCTCTTGTTGCCCAGGCTTGAGTGCAATGGCAC T C SYNRG Ensembl:ENSG00000275066 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1196617896 Functional Loss SNV dbSNP153 33..33 33 - - - 50280 RMVar_ID_50280 Human_SNP_ID_623402926 A-to-I Human chr17 - 37544446 37544446 37544446 GCCAGGCGTGGTGGCGGCTGCCTGTAATCCCAACTAATCGAGAGGCTGAGACCGGAGAATCGCTT GCCAGGCGTGGTGGCGGCTGCCTGTAATCCCAGCTAATCGAGAGGCTGAGACCGGAGAATCGCTT T C SYNRG Ensembl:ENSG00000275066 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041991040 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4289,RMVar_hsa_circ_55240,RMVar_hsa_circ_183770,RMVar_hsa_circ_67969,RMVar_hsa_circ_371261 50281 RMVar_ID_50281 Human_SNP_ID_623403839 A-to-I Human chr17 - 37548818 37548816 37548818 TTGTGTGTTTTTTTTTTTTTTTTTTAAGACAGAGTTTCCCTCTTGTCACCCAGGCTGGAGTGGAA TTGTGTGTTTTTTTTTTTTTTTTTTAAGACAG__TTTCCCTCTTGTCACCCAGGCTGGAGTGGAA ACT A SYNRG Ensembl:ENSG00000275066 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs764344968 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_4289,RMVar_hsa_circ_55240,RMVar_hsa_circ_183770,RMVar_hsa_circ_67969,RMVar_hsa_circ_371261 50282 RMVar_ID_50282 Human_SNP_ID_623403840 A-to-I Human chr17 - 37548818 37548817 37548818 TTGTGTGTTTTTTTTTTTTTTTTTTAAGACAGAGTTTCCCTCTTGTCACCCAGGCTGGAGTGGAA TTGTGTGTTTTTTTTTTTTTTTTTTAAGACAG_GTTTCCCTCTTGTCACCCAGGCTGGAGTGGAA CT C SYNRG Ensembl:ENSG00000275066 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1342002412 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_4289,RMVar_hsa_circ_55240,RMVar_hsa_circ_183770,RMVar_hsa_circ_67969,RMVar_hsa_circ_371261 50283 RMVar_ID_50283 Human_SNP_ID_623406235 A-to-I Human chr17 - 37559651 37559651 37559651 AGTTTTATTTTTGTCAACCAGGCTAGAGTGCAATGGCATGATCTTGGCTCACTGCAACCTCCACC AGTTTTATTTTTGTCAACCAGGCTAGAGTGCAGTGGCATGATCTTGGCTCACTGCAACCTCCACC T C SYNRG Ensembl:ENSG00000275066 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1039742845 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4289,RMVar_hsa_circ_55240,RMVar_hsa_circ_67156,RMVar_hsa_circ_67969,RMVar_hsa_circ_338919,RMVar_hsa_circ_356939,RMVar_hsa_circ_52066,RMVar_hsa_circ_183771 50284 RMVar_ID_50284 Human_SNP_ID_623406236 A-to-I Human chr17 - 37559659 37559659 37559659 TGAAACAGAGTTTTATTTTTGTCAACCAGGCTAGAGTGCAATGGCATGATCTTGGCTCACTGCAA TGAAACAGAGTTTTATTTTTGTCAACCAGGCTGGAGTGCAATGGCATGATCTTGGCTCACTGCAA T C SYNRG Ensembl:ENSG00000275066 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1324526282 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4289,RMVar_hsa_circ_55240,RMVar_hsa_circ_67156,RMVar_hsa_circ_67969,RMVar_hsa_circ_338919,RMVar_hsa_circ_356939,RMVar_hsa_circ_52066,RMVar_hsa_circ_183771 50285 RMVar_ID_50285 Human_SNP_ID_623413715 A-to-I Human chr17 - 37589561 37589561 37589561 GTATTTTAGTAGAGATGGGATTTCATCGTGTTAGCCAGGATGGTCTTGATCTCCTGACCTGGTGA GTATTTTAGTAGAGATGGGATTTCATCGTGTTGGCCAGGATGGTCTTGATCTCCTGACCTGGTGA T C SYNRG Ensembl:ENSG00000275066 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005257526 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12560,RMVar_hsa_circ_292856 50286 RMVar_ID_50286 Human_SNP_ID_623419009 A-to-I Human chr17 - 37610186 37610186 37610186 CAGGGAGGCTGAGGCTGCTGTGAGCCATGATCATGCCACTGCACTCCAGCCTGGACAACAGAGCA CAGGGAGGCTGAGGCTGCTGTGAGCCATGATCGTGCCACTGCACTCCAGCCTGGACAACAGAGCA T C DDX52 Ensembl:ENSG00000278053 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs769640206 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9858728,Human_RBP_ID_25341375 50287 RMVar_ID_50287 Human_SNP_ID_623419524 A-to-I Human chr17 - 37611867 37611867 37611867 AGCCTTGACCTCTTAGACTCAAGTGATCCTCAAACCTCAGCCTCCCGAGTAGCTGGTACTATAGG AGCCTTGACCTCTTAGACTCAAGTGATCCTCACACCTCAGCCTCCCGAGTAGCTGGTACTATAGG T G DDX52 Ensembl:ENSG00000278053 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1425038948 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12987165 50288 RMVar_ID_50288 Human_SNP_ID_623419535 A-to-I Human chr17 - 37611904 37611904 37611904 TAATTTGGAGTTTAGTGGCACAATCATGGCCCACTGCAGCCTTGACCTCTTAGACTCAAGTGATC TAATTTGGAGTTTAGTGGCACAATCATGGCCCGCTGCAGCCTTGACCTCTTAGACTCAAGTGATC T C DDX52 Ensembl:ENSG00000278053 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984578445 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6589247,Human_RBP_ID_12987166 50289 RMVar_ID_50289 Human_SNP_ID_623419710 A-to-I Human chr17 - 37612343 37612343 37612343 GCCAGGCGTAGTGGCTCATGCCTGTAATCCTAACACTTCGGGAGGCCTAGGCGGGCAGGTTGTCT GCCAGGCGTAGTGGCTCATGCCTGTAATCCTAGCACTTCGGGAGGCCTAGGCGGGCAGGTTGTCT T C DDX52 Ensembl:ENSG00000278053 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs975424089 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238410,Human_RBP_ID_6589255,Human_RBP_ID_12987176 50290 RMVar_ID_50290 Human_SNP_ID_623419715 A-to-I Human chr17 - 37612366 37612366 37612366 ATTTATTGAAAATATTTTTCTTGGCCAGGCGTAGTGGCTCATGCCTGTAATCCTAACACTTCGGG ATTTATTGAAAATATTTTTCTTGGCCAGGCGTCGTGGCTCATGCCTGTAATCCTAACACTTCGGG T G DDX52 Ensembl:ENSG00000278053 Protein coding 3'UTR GSE38233;GSE99789;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29796672,31158229 RNA-Seq:(High) rs556861106 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238410 50291 RMVar_ID_50291 Human_SNP_ID_623419718 A-to-I Human chr17 - 37612372 37612372 37612372 TACTAAATTTATTGAAAATATTTTTCTTGGCCAGGCGTAGTGGCTCATGCCTGTAATCCTAACAC TACTAAATTTATTGAAAATATTTTTCTTGGCCTGGCGTAGTGGCTCATGCCTGTAATCCTAACAC T A DDX52 Ensembl:ENSG00000278053 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1449544964 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12987177 50292 RMVar_ID_50292 Human_SNP_ID_623420057 A-to-I Human chr17 - 37614041 37614041 37614041 CCAGGCTGGTCTTGAACTCCTGACCTCACACAATCCTCCTGCCTTAGCCTCCTGAGTAACTGAGA CCAGGCTGGTCTTGAACTCCTGACCTCACACAGTCCTCCTGCCTTAGCCTCCTGAGTAACTGAGA T C DDX52 Ensembl:ENSG00000278053 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1247656225 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_134762,Human_RBP_ID_24416415,Human_RBP_ID_25277573,Human_RBP_ID_26449684 Human_miRNA_ID_86349,Human_miRNA_ID_629638,Human_miRNA_ID_1024455,Human_miRNA_ID_1078435,Human_miRNA_ID_1502632 50293 RMVar_ID_50293 Human_SNP_ID_623420069 A-to-I Human chr17 - 37614091 37614091 37614091 TGTAGGTGCCTTTTTTTTTTCCTGTAGAGATGAGGGTCTTGCCATGTTGTCCAGGCTGGTCTTGA TGTAGGTGCCTTTTTTTTTTCCTGTAGAGATGGGGGTCTTGCCATGTTGTCCAGGCTGGTCTTGA T C DDX52 Ensembl:ENSG00000278053 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432979668 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_134762,Human_RBP_ID_1856495,Human_RBP_ID_6589291,Human_RBP_ID_12987249,Human_RBP_ID_17890826,Human_RBP_ID_24416415 50294 RMVar_ID_50294 Human_SNP_ID_623420070 A-to-I Human chr17 - 37614096 37614093 37614097 CAATTTGTAGGTGCCTTTTTTTTTTCCTGTAGAGATGAGGGTCTTGCCATGTTGTCCAGGCTGGT CAATTTGTAGGTGCCTTTTTTTTTTCCTGTA____TGAGGGTCTTGCCATGTTGTCCAGGCTGGT ATCTC A DDX52 Ensembl:ENSG00000278053 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1555807852 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_134762,Human_RBP_ID_1856495,Human_RBP_ID_6589291,Human_RBP_ID_12987249,Human_RBP_ID_17890826,Human_RBP_ID_18291584,Human_RBP_ID_24416415 50295 RMVar_ID_50295 Human_SNP_ID_623420072 A-to-I Human chr17 - 37614098 37614098 37614098 TTCAATTTGTAGGTGCCTTTTTTTTTTCCTGTAGAGATGAGGGTCTTGCCATGTTGTCCAGGCTG TTCAATTTGTAGGTGCCTTTTTTTTTTCCTGTTGAGATGAGGGTCTTGCCATGTTGTCCAGGCTG T A DDX52 Ensembl:ENSG00000278053 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1462302589 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1856495,Human_RBP_ID_6589291,Human_RBP_ID_12987249,Human_RBP_ID_17890826,Human_RBP_ID_18291584,Human_RBP_ID_24416415,Human_RBP_ID_24478707,Human_RBP_ID_25341381 Human_miRNA_ID_275786 50296 RMVar_ID_50296 Human_SNP_ID_623520910 A-to-I Human chr17 - 38200004 38200004 38200004 AAAATTAGCTGGGCGTGGTGGTATGCACCTGTAATCCTAGCTACTCTGGAGGTTGAGGCAGAAGA AAAATTAGCTGGGCGTGGTGGTATGCACCTGTGATCCTAGCTACTCTGGAGGTTGAGGCAGAAGA T C NPEPPSP1 Ensembl:ENSG00000274487 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1142837 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8254152,Human_RBP_ID_17378982,Human_RBP_ID_21976575,Human_RBP_ID_25277964 RMVar_hsa_circ_55626,RMVar_hsa_circ_321088,RMVar_hsa_circ_9308 50297 RMVar_ID_50297 Human_SNP_ID_623524980 A-to-I Human chr17 - 38218203 38218203 38218203 CTATAATCCCAGCTACTCAGAAGGCTGAGGCAAGAAAATCGCCAGAAGTCAGGAAGTGGAGGTTG CTATAATCCCAGCTACTCAGAAGGCTGAGGCAGGAAAATCGCCAGAAGTCAGGAAGTGGAGGTTG T C NPEPPSP1 Ensembl:ENSG00000274487 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417913786 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55626,RMVar_hsa_circ_67847 50298 RMVar_ID_50298 Human_SNP_ID_623528442 A-to-I Human chr17 - 38233915 38233915 38233915 TGTTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGAATGGTCTCCATCTTCTGACCTCGTGA TGTTTTTAGTAGAGACGGGGTTTCACCGTGTTGGCCAGAATGGTCTCCATCTTCTGACCTCGTGA T C NPEPPSP1 Ensembl:ENSG00000274487 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs541963016 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67847,RMVar_hsa_circ_336967 50299 RMVar_ID_50299 Human_SNP_ID_623534119 A-to-I Human chr17 - 38255966 38255966 38255966 GAGTTCGAGACCAGCCTGACCAACATGGTGAAACCCCCGTCTCTACTAAAAATACAAAAATTATC GAGTTCGAGACCAGCCTGACCAACATGGTGAACCCCCCGTCTCTACTAAAAATACAAAAATTATC T G NPEPPSP1 Ensembl:ENSG00000274487 Pseudogene intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1384476542 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18514483 50300 RMVar_ID_50300 Human_SNP_ID_623546838 A-to-I Human chr17 + 38304621 38304621 38304621 GCTGGATTGCAGTGGCGCGATCTTGACTTACTACAACCTCTGCCTCTTGGGTTCAAACAATTTTC GCTGGATTGCAGTGGCGCGATCTTGACTTACTGCAACCTCTGCCTCTTGGGTTCAAACAATTTTC A G MRPL45 Ensembl:ENSG00000278845 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1287915827 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_55307,RMVar_hsa_circ_56516,RMVar_hsa_circ_315371,RMVar_hsa_circ_24084,RMVar_hsa_circ_363934 50301 RMVar_ID_50301 Human_SNP_ID_623549382 A-to-I Human chr17 + 38313482 38313481 38313482 GGGCTTAAGCAATCCTCTTGCCTCGGCCTCCCAAAATGCTAGGACTACAGGTGTGAGCCACCATG GGGCTTAAGCAATCCTCTTGCCTCGGCCTCCC_AAATGCTAGGACTACAGGTGTGAGCCACCATG CA C MRPL45 Ensembl:ENSG00000278845 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1219325978 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_55307,RMVar_hsa_circ_56516,RMVar_hsa_circ_24084,RMVar_hsa_circ_358327 50302 RMVar_ID_50302 Human_SNP_ID_623599803 A-to-I Human chr17 + 38505104 38505104 38505104 ACAGCTCACTGCAGCCTCTAACTGCTGTGCTCAAGTGATCCTCCTGCTTCAACCTCCTGAGTTAG ACAGCTCACTGCAGCCTCTAACTGCTGTGCTCTAGTGATCCTCCTGCTTCAACCTCCTGAGTTAG A T ARHGAP23 Ensembl:ENSG00000275832 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1316053091 Functional Loss SNV dbSNP153 33..33 33 - - - 50303 RMVar_ID_50303 Human_SNP_ID_623607900 A-to-I Human chr17 - 38535355 38535355 38535355 AAAAACACAAAATTAGCCGGGCGTGGTGGCGCATGCCTGTAATTCCAGCTACTCGGGAGGCTGAG AAAAACACAAAATTAGCCGGGCGTGGTGGCGCGTGCCTGTAATTCCAGCTACTCGGGAGGCTGAG T C SRCIN1 Ensembl:ENSG00000277363 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1209284317 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_134754 50304 RMVar_ID_50304 Human_SNP_ID_623659573 A-to-I Human chr17 + 38734042 38734042 38734042 TCAGGGGGCTCCCAACCCCACACACCTACGCTATGATGGAATCTCGAGTCTCGACTCCCGACTCC TCAGGGGGCTCCCAACCCCACACACCTACGCTGTGATGGAATCTCGAGTCTCGACTCCCGACTCC A G CISD3 Ensembl:ENSG00000277972 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs939850570 Functional Loss SNV dbSNP153 33..33 33 - - - 50305 RMVar_ID_50305 Human_SNP_ID_623660037 A-to-I Human chr17 - 38735521 38735521 38735521 GCTCACCCTAGCCACGGTGCCCACCCCCTCCGAGGGCACCAACACCAGCGGGGCGTCCGAGTGTG GCTCACCCTAGCCACGGTGCCCACCCCCTCCGTGGGCACCAACACCAGCGGGGCGTCCGAGTGTG T A PCGF2 Ensembl:ENSG00000277258 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs769007309 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27253190 Human_Splice_Rec_1809908,Human_Splice_Rec_1809928,Human_Splice_Rec_1809929,Human_Splice_Rec_1809946,Human_Splice_Rec_1809966,Human_Splice_Rec_1809984,Human_Splice_Rec_1810000 50306 RMVar_ID_50306 Human_SNP_ID_623662895 A-to-I Human chr17 - 38745021 38745021 38745021 TTTAGTAGAGATGGGGTTTCACCATCTTTGCCAGCCTGGTTTTGAACTCCTGACCTCATGATCCA TTTAGTAGAGATGGGGTTTCACCATCTTTGCCCGCCTGGTTTTGAACTCCTGACCTCATGATCCA T G PCGF2 Ensembl:ENSG00000277258 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1300576582 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4026,RMVar_hsa_circ_268490 50307 RMVar_ID_50307 Human_SNP_ID_623665279 A-to-I Human chr17 + 38753502 38753502 38753502 TGTCCTTCCCTTTCTTTTTTTTTTTTTTAGACAGGGACTTGCTCTGTCACCCAGGCTGGAGCTCA TGTCCTTCCCTTTCTTTTTTTTTTTTTTAGACGGGGACTTGCTCTGTCACCCAGGCTGGAGCTCA A G PSMB3 Ensembl:ENSG00000277791 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893280571 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88325,RMVar_hsa_circ_183818,RMVar_hsa_circ_91349,RMVar_hsa_circ_183819 50308 RMVar_ID_50308 Human_SNP_ID_623665280 A-to-I Human chr17 + 38753502 38753502 38753502 TGTCCTTCCCTTTCTTTTTTTTTTTTTTAGACAGGGACTTGCTCTGTCACCCAGGCTGGAGCTCA TGTCCTTCCCTTTCTTTTTTTTTTTTTTAGACTGGGACTTGCTCTGTCACCCAGGCTGGAGCTCA A T PSMB3 Ensembl:ENSG00000277791 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893280571 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88325,RMVar_hsa_circ_183818,RMVar_hsa_circ_91349,RMVar_hsa_circ_183819 50309 RMVar_ID_50309 Human_SNP_ID_623665306 A-to-I Human chr17 + 38753578 38753578 38753578 TCAGCTCACTGCAACCTCCACCTCCCAGGCTCAAGCGATTCTCGTGCCTCAGCCTCCTAAGTAGC TCAGCTCACTGCAACCTCCACCTCCCAGGCTCCAGCGATTCTCGTGCCTCAGCCTCCTAAGTAGC A C PSMB3 Ensembl:ENSG00000277791 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1183438907 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88325,RMVar_hsa_circ_183818,RMVar_hsa_circ_91349,RMVar_hsa_circ_183819 50310 RMVar_ID_50310 Human_SNP_ID_623666518 A-to-I Human chr17 + 38757398 38757398 38757398 AAAATTAGCTGGGTGTGGTGGTGCACGCCTGTAATCCCAGCCACTCGGGAAGCTGAAGCATGAGA AAAATTAGCTGGGTGTGGTGGTGCACGCCTGTGATCCCAGCCACTCGGGAAGCTGAAGCATGAGA A G PSMB3 Ensembl:ENSG00000277791 Protein coding intron GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-Seq:(High) rs1186438887 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88325,RMVar_hsa_circ_183818,RMVar_hsa_circ_91349,RMVar_hsa_circ_183819,RMVar_hsa_circ_183820,RMVar_hsa_circ_95821 50311 RMVar_ID_50311 Human_SNP_ID_623666534 A-to-I Human chr17 + 38757467 38757467 38757467 TTGAACTTGGGAGGCAGAGGTTGTAGTGAGCCAAGATCATGCCACTGTACTCCAGCCTTGGTGAC TTGAACTTGGGAGGCAGAGGTTGTAGTGAGCCGAGATCATGCCACTGTACTCCAGCCTTGGTGAC A G PSMB3 Ensembl:ENSG00000277791 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs189355653 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22960728,Human_RBP_ID_25341532 RMVar_hsa_circ_88325,RMVar_hsa_circ_183818,RMVar_hsa_circ_91349,RMVar_hsa_circ_183819,RMVar_hsa_circ_183820,RMVar_hsa_circ_95821 50312 RMVar_ID_50312 Human_SNP_ID_623666662 A-to-I Human chr17 + 38757906 38757906 38757906 TCAAACTCATGACCTCATGATCCGCCCACCTCAGCCTCCCAAAGTGCTGGGATTACAAGCATGAA TCAAACTCATGACCTCATGATCCGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAAGCATGAA A G PSMB3 Ensembl:ENSG00000277791 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1171530464 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_88325,RMVar_hsa_circ_183818,RMVar_hsa_circ_91349,RMVar_hsa_circ_183819,RMVar_hsa_circ_183820,RMVar_hsa_circ_95821 50313 RMVar_ID_50313 Human_SNP_ID_623668062 A-to-I Human chr17 + 38763782 38763782 38763782 CTCAGGCCTCCCAAAGTGCTGGGATTGCAAGCATGAGCCACCGCGCCCGGCCAAGCTCCTTCCCT CTCAGGCCTCCCAAAGTGCTGGGATTGCAAGCGTGAGCCACCGCGCCCGGCCAAGCTCCTTCCCT A G PSMB3 Ensembl:ENSG00000277791 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs935653276 Functional Loss SNV dbSNP153 33..33 33 - - - 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_183822,RMVar_hsa_circ_183824,RMVar_hsa_circ_87379 50314 RMVar_ID_50314 Human_SNP_ID_623668820 A-to-I Human chr17 - 38767049 38767048 38767049 GGCATCTCAGAATAATGTTGGGTCTCCCAAGAAGAAAGGTGTAAGAATAACGACATGGCTGATTA GGCATCTCAGAATAATGTTGGGTCTCCCAAGA_GAAAGGTGTAAGAATAACGACATGGCTGATTA CT C PIP4K2B Ensembl:ENSG00000276293 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1360046943 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_1532831,Human_RBP_ID_1856711,Human_RBP_ID_18291703 RMVar_hsa_circ_124604,RMVar_hsa_circ_183827,RMVar_hsa_circ_95216,RMVar_hsa_circ_183826 50315 RMVar_ID_50315 Human_SNP_ID_623670949 A-to-I Human chr17 - 38776063 38776063 38776063 GGGAGGCTGAGGCAAGAGAATCGCTTGAACCCAGGAGGCGGAGGTTGCGGTGACCCTCCAGCTTG GGGAGGCTGAGGCAAGAGAATCGCTTGAACCCGGGAGGCGGAGGTTGCGGTGACCCTCCAGCTTG T C PIP4K2B Ensembl:ENSG00000276293 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1244174237 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_78353,RMVar_hsa_circ_183827,RMVar_hsa_circ_95216,RMVar_hsa_circ_47143,RMVar_hsa_circ_99057,RMVar_hsa_circ_183830,RMVar_hsa_circ_112256,RMVar_hsa_circ_183831,RMVar_hsa_circ_183832 50316 RMVar_ID_50316 Human_SNP_ID_623673703 A-to-I Human chr17 - 38787068 38787068 38787068 TCATGCCACTGCACTTCAGCCTGGGTGACAGAATGAGACCCTGTCTCAAAAAAACAAAAAAAGAC TCATGCCACTGCACTTCAGCCTGGGTGACAGAGTGAGACCCTGTCTCAAAAAAACAAAAAAAGAC T C PIP4K2B Ensembl:ENSG00000276293 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs112347533 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183840 50317 RMVar_ID_50317 Human_SNP_ID_623674217 A-to-I Human chr17 - 38789113 38789113 38789113 CCCTGCTTTATTTTATTTTCTTTTTTGAGACAAGATCTCACTCTTGCCCAGGCTAGAGTGCAGTG CCCTGCTTTATTTTATTTTCTTTTTTGAGACACGATCTCACTCTTGCCCAGGCTAGAGTGCAGTG T G PIP4K2B Ensembl:ENSG00000276293 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444720224 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6590238,Human_RBP_ID_12990047 RMVar_hsa_circ_183840 50318 RMVar_ID_50318 Human_SNP_ID_623674537 A-to-I Human chr17 - 38790442 38790442 38790442 GACCTCGTGATCCGTCCCCTTAGGCCTCCCAAAGTGTTGGGATTATAGGCGTGAGCCACTGCGCC GACCTCGTGATCCGTCCCCTTAGGCCTCCCAACGTGTTGGGATTATAGGCGTGAGCCACTGCGCC T G PIP4K2B Ensembl:ENSG00000276293 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1172002179 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23308236 RMVar_hsa_circ_183840 50319 RMVar_ID_50319 Human_SNP_ID_623674635 A-to-I Human chr17 - 38790736 38790736 38790736 TTTCCTAGGCTGGGCCAGGTGCAGTAGCTCACATCTGTAATCCCAGCATTTTGGGAGGCTGAGGC TTTCCTAGGCTGGGCCAGGTGCAGTAGCTCACGTCTGTAATCCCAGCATTTTGGGAGGCTGAGGC T C PIP4K2B Ensembl:ENSG00000276293 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893386529 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183840 50320 RMVar_ID_50320 Human_SNP_ID_623674948 A-to-I Human chr17 - 38791922 38791922 38791922 TCCGTTAATTTTTTTTTGTATTTTTTTTTAGTAGAGACGGGGTTTCACTGTGTTAGCCAGGATGG TCCGTTAATTTTTTTTTGTATTTTTTTTTAGTGGAGACGGGGTTTCACTGTGTTAGCCAGGATGG T C PIP4K2B Ensembl:ENSG00000276293 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs529554233 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183840 50321 RMVar_ID_50321 Human_SNP_ID_623674963 A-to-I Human chr17 - 38791974 38791974 38791974 CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGTGCCCGCCATCATGCTCCGTTAATTTTT CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTGCAGGTGCCCGCCATCATGCTCCGTTAATTTTT T C PIP4K2B Ensembl:ENSG00000276293 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285709676 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183840 50322 RMVar_ID_50322 Human_SNP_ID_623675025 A-to-I Human chr17 - 38792201 38792201 38792201 GAGGCTGCAGTGAGCTGAGATCATACCACTGCACTCTAGCCTGGCCTATGGAAGTGAGACCCTGT GAGGCTGCAGTGAGCTGAGATCATACCACTGCCCTCTAGCCTGGCCTATGGAAGTGAGACCCTGT T G PIP4K2B Ensembl:ENSG00000276293 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1434912245 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12990084,Human_RBP_ID_17566835 RMVar_hsa_circ_183840 50323 RMVar_ID_50323 Human_SNP_ID_623675439 A-to-I Human chr17 - 38793749 38793749 38793749 CTCCTGCCTTAGCCACCCGAGTAGCTGGGACTACAGGCACATGCCACCACACCCGACTAACACTT CTCCTGCCTTAGCCACCCGAGTAGCTGGGACTGCAGGCACATGCCACCACACCCGACTAACACTT T C PIP4K2B Ensembl:ENSG00000276293 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs531504279 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183840 50324 RMVar_ID_50324 Human_SNP_ID_623678798 A-to-I Human chr17 - 38805951 38805951 38805951 AAAATTAGTTGGTCATGGTGGCACATGCCTGTAATCCCAGTTATTTGGGAGGCTGAGACAGGAGA AAAATTAGTTGGTCATGGTGGCACATGCCTGTGATCCCAGTTATTTGGGAGGCTGAGACAGGAGA T C CWC25 Ensembl:ENSG00000273559 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1041263649 Functional Loss SNV dbSNP153 33..33 33 - - - 50325 RMVar_ID_50325 Human_SNP_ID_623691098 A-to-I Human chr17 - 38848508 38848508 38848508 TAAATCTCGCCTGGGTACGGTGGCTCACACCTATAATCCCAGCACTTTGGGAGGCTGAGGTGGGT TAAATCTCGCCTGGGTACGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGT T C RPL23 Ensembl:ENSG00000125691 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1365282741 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25278824 50326 RMVar_ID_50326 Human_SNP_ID_623691330 A-to-I Human chr17 - 38849475 38849475 38849475 AAATTAGCTGGGCGTGGTGGCGCACCGCCTGTAATCTCAGCTACTGAGAGAATCGCTTGAACCTG AAATTAGCTGGGCGTGGTGGCGCACCGCCTGTTATCTCAGCTACTGAGAGAATCGCTTGAACCTG T A RPL23 Ensembl:ENSG00000125691 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs923465983 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2529447,Human_RBP_ID_12990612,Human_RBP_ID_27451544 50327 RMVar_ID_50327 Human_SNP_ID_623691350 A-to-I Human chr17 - 38849515 38849515 38849515 TGACCAACGTGGTGAAACCTCCTCTTTTCTAAAAATACAAAAATTAGCTGGGCGTGGTGGCGCAC TGACCAACGTGGTGAAACCTCCTCTTTTCTAACAATACAAAAATTAGCTGGGCGTGGTGGCGCAC T G RPL23 Ensembl:ENSG00000125691 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1221362071 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25278844 50328 RMVar_ID_50328 Human_SNP_ID_623691357 A-to-I Human chr17 - 38849532 38849532 38849532 GGAGTTCAAGACCAGGCTGACCAACGTGGTGAAACCTCCTCTTTTCTAAAAATACAAAAATTAGC GGAGTTCAAGACCAGGCTGACCAACGTGGTGAGACCTCCTCTTTTCTAAAAATACAAAAATTAGC T C RPL23 Ensembl:ENSG00000125691 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs754220446 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12990617 50329 RMVar_ID_50329 Human_SNP_ID_623691367 A-to-I Human chr17 - 38849557 38849557 38849557 CCAAGGCAGGCAGATCATGAGGTCAGGAGTTCAAGACCAGGCTGACCAACGTGGTGAAACCTCCT CCAAGGCAGGCAGATCATGAGGTCAGGAGTTCGAGACCAGGCTGACCAACGTGGTGAAACCTCCT T C RPL23 Ensembl:ENSG00000125691 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1555551321 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25278846,Human_RBP_ID_26449862 50330 RMVar_ID_50330 Human_SNP_ID_623691372 A-to-I Human chr17 - 38849586 38849586 38849586 GGCACCTGTAATCCCAACACTTTCGGAGGCCAAGGCAGGCAGATCATGAGGTCAGGAGTTCAAGA GGCACCTGTAATCCCAACACTTTCGGAGGCCAGGGCAGGCAGATCATGAGGTCAGGAGTTCAAGA T C RPL23 Ensembl:ENSG00000125691 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1463545963 Functional Loss SNV dbSNP153 33..33 33 - - - 50331 RMVar_ID_50331 Human_SNP_ID_623691483 A-to-I Human chr17 - 38850018 38850018 38850018 CACTTCCAGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTAAGTAGCTGGGATTACAGGCACCTG CACTTCCAGGGTTCAAGCGATTCTCCTGCCTCGGCCTCCTAAGTAGCTGGGATTACAGGCACCTG T C RPL23 Ensembl:ENSG00000125691 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1325771425 Functional Loss SNV dbSNP153 33..33 33 - - - 50332 RMVar_ID_50332 Human_SNP_ID_623707681 A-to-I Human chr17 + 38909801 38909801 38909801 AGATGGACTCACTCTGTCTCCCAGGCTGGAGTACAGTGGCTCGATCTCAGCTCACTGCAATCTCC AGATGGACTCACTCTGTCTCCCAGGCTGGAGTGCAGTGGCTCGATCTCAGCTCACTGCAATCTCC A G LASP1 Ensembl:ENSG00000002834 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1307085440 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127058,RMVar_hsa_circ_183848,RMVar_hsa_circ_183852 50333 RMVar_ID_50333 Human_SNP_ID_623709908 A-to-I Human chr17 + 38917819 38917819 38917819 TGAAGCCATCCTCCCACCTCAGCCTCCTGAGTAGCTGAGACTACAGGCATGTACCACTAAGCCTA TGAAGCCATCCTCCCACCTCAGCCTCCTGAGTGGCTGAGACTACAGGCATGTACCACTAAGCCTA A G LASP1 Ensembl:ENSG00000002834 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1050167663 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127058,RMVar_hsa_circ_183848,RMVar_hsa_circ_125964,RMVar_hsa_circ_183854 50334 RMVar_ID_50334 Human_SNP_ID_623709946 A-to-I Human chr17 + 38918009 38918009 38918009 AAAAAGTACAAAAATTAGCCGGGCATGGTGGTACACGCTTATAGTCCCAGCTACTTGGGAGGCTG AAAAAGTACAAAAATTAGCCGGGCATGGTGGTGCACGCTTATAGTCCCAGCTACTTGGGAGGCTG A G LASP1 Ensembl:ENSG00000002834 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs574242860 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127058,RMVar_hsa_circ_183848,RMVar_hsa_circ_125964,RMVar_hsa_circ_183854 50335 RMVar_ID_50335 Human_SNP_ID_623714398 A-to-I Human chr17 - 38934076 38934076 38934076 ACAAGCCCGGCCAAGAGACCAGCCTGGCCAACATGGTGAAACCCTATCTCTACTAAAAATACAAA ACAAGCCCGGCCAAGAGACCAGCCTGGCCAACGTGGTGAAACCCTATCTCTACTAAAAATACAAA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417808611 Functional Loss SNV dbSNP153 33..33 33 - - - 50336 RMVar_ID_50336 Human_SNP_ID_623776364 A-to-I Human chr17 - 39178457 39178457 39178457 GGGCTCGCTTGAGCCCAGGGTAGAGGTGAACTATGTTCACACCACTGCACTTCAGCCTGGGTGAC GGGCTCGCTTGAGCCCAGGGTAGAGGTGAACTGTGTTCACACCACTGCACTTCAGCCTGGGTGAC T C CACNB1 Ensembl:ENSG00000067191 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs986933222 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183858,RMVar_hsa_circ_123753 50337 RMVar_ID_50337 Human_SNP_ID_623776365 A-to-I Human chr17 - 39178460 39178460 39178460 TGGGGGCTCGCTTGAGCCCAGGGTAGAGGTGAACTATGTTCACACCACTGCACTTCAGCCTGGGT TGGGGGCTCGCTTGAGCCCAGGGTAGAGGTGATCTATGTTCACACCACTGCACTTCAGCCTGGGT T A CACNB1 Ensembl:ENSG00000067191 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1165648390 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183858,RMVar_hsa_circ_123753 50338 RMVar_ID_50338 Human_SNP_ID_623776376 A-to-I Human chr17 - 39178518 39178518 39178518 AAAATTAGTGGGGTATGATGGCACGTGCCTGTAGCCCTAGTTACTGAGGAGGCTAGGCTGGGGGC AAAATTAGTGGGGTATGATGGCACGTGCCTGTGGCCCTAGTTACTGAGGAGGCTAGGCTGGGGGC T C CACNB1 Ensembl:ENSG00000067191 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,31158229,31158229 RNA-Seq:(High) rs1435586080 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183858,RMVar_hsa_circ_123753 50339 RMVar_ID_50339 Human_SNP_ID_623776421 A-to-I Human chr17 - 39178658 39178658 39178658 GAGGGTGTGGCTGGGCTCAGTGACTCACGCCTATAATCCCAGCACTTTGAGAGGCTGAGGCAAGT GAGGGTGTGGCTGGGCTCAGTGACTCACGCCTGTAATCCCAGCACTTTGAGAGGCTGAGGCAAGT T C CACNB1 Ensembl:ENSG00000067191 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1244338011 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183858,RMVar_hsa_circ_123753 50340 RMVar_ID_50340 Human_SNP_ID_623776533 A-to-I Human chr17 - 39179104 39179104 39179104 TATTTTTAGTAGAGATGGGGTTTCACCATGTTAGCCAGGATGGTCTCGATCTCCTGACTTCAAGA TATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGATGGTCTCGATCTCCTGACTTCAAGA T C CACNB1 Ensembl:ENSG00000067191 Protein coding intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1371039698 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183858,RMVar_hsa_circ_123753 50341 RMVar_ID_50341 Human_SNP_ID_623776553 A-to-I Human chr17 - 39179176 39179176 39179176 CCATTCTTCTGCCCCAGCCTCCTGAGTAGCTGAGACTACAGGCGCCTACCACCACATCCGGCTAA CCATTCTTCTGCCCCAGCCTCCTGAGTAGCTGGGACTACAGGCGCCTACCACCACATCCGGCTAA T C CACNB1 Ensembl:ENSG00000067191 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs921616971 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183858,RMVar_hsa_circ_123753 50342 RMVar_ID_50342 Human_SNP_ID_623777089 A-to-I Human chr17 - 39181295 39181295 39181295 GAGCTAAAGAGTTCAAGACCAGCCTGGGCAACATGATGAAACCCTGCCTCTACTAAAATTCAAAA GAGCTAAAGAGTTCAAGACCAGCCTGGGCAACTTGATGAAACCCTGCCTCTACTAAAATTCAAAA T A CACNB1 Ensembl:ENSG00000067191 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1204585505 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183858,RMVar_hsa_circ_123753 50343 RMVar_ID_50343 Human_SNP_ID_623777090 A-to-I Human chr17 - 39181295 39181295 39181295 GAGCTAAAGAGTTCAAGACCAGCCTGGGCAACATGATGAAACCCTGCCTCTACTAAAATTCAAAA GAGCTAAAGAGTTCAAGACCAGCCTGGGCAACGTGATGAAACCCTGCCTCTACTAAAATTCAAAA T C CACNB1 Ensembl:ENSG00000067191 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1204585505 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183858,RMVar_hsa_circ_123753 50344 RMVar_ID_50344 Human_SNP_ID_623777092 A-to-I Human chr17 - 39181297 39181297 39181297 CTGAGCTAAAGAGTTCAAGACCAGCCTGGGCAACATGATGAAACCCTGCCTCTACTAAAATTCAA CTGAGCTAAAGAGTTCAAGACCAGCCTGGGCAGCATGATGAAACCCTGCCTCTACTAAAATTCAA T C CACNB1 Ensembl:ENSG00000067191 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1275425246 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183858,RMVar_hsa_circ_123753 50345 RMVar_ID_50345 Human_SNP_ID_623777393 A-to-I Human chr17 - 39182553 39182553 39182553 GGACTACAGGAGTGTACCACCACGGCCCGGCTAATTTTTTGTATTTTTTAGTAGAGACAGGGTTT GGACTACAGGAGTGTACCACCACGGCCCGGCTGATTTTTTGTATTTTTTAGTAGAGACAGGGTTT T C CACNB1 Ensembl:ENSG00000067191 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs572177767 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183858,RMVar_hsa_circ_123753 50346 RMVar_ID_50346 Human_SNP_ID_623777408 A-to-I Human chr17 - 39182602 39182602 39182602 CACCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTGGCTGGGACTACAGGAGTGTA CACCTCCCAGGTTCAAGCGATTCTCCTGCCTCTGCCTCCTGAGTGGCTGGGACTACAGGAGTGTA T A CACNB1 Ensembl:ENSG00000067191 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1326413107 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183858,RMVar_hsa_circ_123753 50347 RMVar_ID_50347 Human_SNP_ID_623779620 A-to-I Human chr17 - 39190299 39190299 39190299 CTCCCATCTCAGCCTCCCGAGTACCTGGAACTATAGAGGCATACCACCACACCTGGCTGATTTTT CTCCCATCTCAGCCTCCCGAGTACCTGGAACTGTAGAGGCATACCACCACACCTGGCTGATTTTT T C CACNB1 Ensembl:ENSG00000067191 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1423536882 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_13958,RMVar_hsa_circ_183858,RMVar_hsa_circ_123753,RMVar_hsa_circ_111527,RMVar_hsa_circ_183861 50348 RMVar_ID_50348 Human_SNP_ID_623797104 A-to-I Human chr17 - 39254189 39254189 39254189 TACAAAATCCCAGCTACTTGGGAGGCTGAGGCAAGAGAATCACTTGAACCTGGGAGGCGGATGTT TACAAAATCCCAGCTACTTGGGAGGCTGAGGCTAGAGAATCACTTGAACCTGGGAGGCGGATGTT T A FBXL20 Ensembl:ENSG00000108306 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1316708764 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25279331 50349 RMVar_ID_50349 Human_SNP_ID_623797136 A-to-I Human chr17 - 39254328 39254328 39254328 GAAGAAAACTTTGCAGCCAGGCGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAG GAAGAAAACTTTGCAGCCAGGCGTGGTGGCTCCCGCCTGTAATCCCAGCACTTTGGGAGGCCGAG T G FBXL20 Ensembl:ENSG00000108306 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1356997670 Functional Loss SNV dbSNP153 33..33 33 - - - 50350 RMVar_ID_50350 Human_SNP_ID_623797506 A-to-I Human chr17 - 39255785 39255785 39255785 CAGGCTGGAGTGCAATAGTGAGATCTCGGCTCACCGCAACCTCCGCCTCTTGGGTTCAAGCGATT CAGGCTGGAGTGCAATAGTGAGATCTCGGCTCGCCGCAACCTCCGCCTCTTGGGTTCAAGCGATT T C FBXL20 Ensembl:ENSG00000108306 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1244840388 Functional Loss SNV dbSNP153 33..33 33 - - - 50351 RMVar_ID_50351 Human_SNP_ID_623797600 A-to-I Human chr17 - 39256155 39256155 39256155 CACCACGCCCAGCTAATGTTTGTATTTTTCATAGAGATGGGGTTTTGCCATGTTGGCCAGGCTAG CACCACGCCCAGCTAATGTTTGTATTTTTCATGGAGATGGGGTTTTGCCATGTTGGCCAGGCTAG T C FBXL20 Ensembl:ENSG00000108306 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs746962882 Functional Loss SNV dbSNP153 33..33 33 - - - 50352 RMVar_ID_50352 Human_SNP_ID_623797617 A-to-I Human chr17 - 39256221 39256221 39256221 TGCCTCCTGGGTTCAAGTGATTCTTCTGTTTCAGCCTCCCAAGAGGCCAGGATTACAGGTGCCCA TGCCTCCTGGGTTCAAGTGATTCTTCTGTTTCGGCCTCCCAAGAGGCCAGGATTACAGGTGCCCA T C FBXL20 Ensembl:ENSG00000108306 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1276606162 Functional Loss SNV dbSNP153 33..33 33 - - - 50353 RMVar_ID_50353 Human_SNP_ID_623797868 A-to-I Human chr17 - 39257216 39257216 39257216 TTGTTATGGCCCGGCACGGTGGGTGGATCACAAGGTCAGGAGTTCAAGAACAGCCTGGCCAAGAT TTGTTATGGCCCGGCACGGTGGGTGGATCACACGGTCAGGAGTTCAAGAACAGCCTGGCCAAGAT T G FBXL20 Ensembl:ENSG00000108306 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1464371941 Functional Loss SNV dbSNP153 33..33 33 - - - 50354 RMVar_ID_50354 Human_SNP_ID_623798426 A-to-I Human chr17 - 39259749 39259749 39259749 GAACTCCTGACCTCAAATGATCCACCTGCCTCAGCCTCCCAAAGTGCTGGGACTACAGGCATGAG GAACTCCTGACCTCAAATGATCCACCTGCCTCGGCCTCCCAAAGTGCTGGGACTACAGGCATGAG T C FBXL20 Ensembl:ENSG00000108306 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs991990320 Functional Loss SNV dbSNP153 33..33 33 - - - 50355 RMVar_ID_50355 Human_SNP_ID_623798964 A-to-I Human chr17 - 39261893 39261893 39261893 TATTTTTAGTAGAAACGGGGTTTCACCATGTTAGCCTGGATGGTCTCAATCTCCTGACCTCGTGA TATTTTTAGTAGAAACGGGGTTTCACCATGTTCGCCTGGATGGTCTCAATCTCCTGACCTCGTGA T G FBXL20 Ensembl:ENSG00000108306 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167088220 Functional Loss SNV dbSNP153 33..33 33 - - - 50356 RMVar_ID_50356 Human_SNP_ID_623799108 A-to-I Human chr17 - 39262508 39262508 39262508 GGGAAGCTGAGGCATGAGGATCACCTGAAGTCAGGAGTTCAAGACCAGCCTGGTCAACATGACGA GGGAAGCTGAGGCATGAGGATCACCTGAAGTCGGGAGTTCAAGACCAGCCTGGTCAACATGACGA T C FBXL20 Ensembl:ENSG00000108306 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs548285145 Functional Loss SNV dbSNP153 33..33 33 - - - 50357 RMVar_ID_50357 Human_SNP_ID_623802063 A-to-I Human chr17 - 39273150 39273150 39273150 TTACAGGCGTGGTGGCCCACTCCTGTAATCCCAGCTACTCGAGAGGCTGAGACAAGAGAACTGTC TTACAGGCGTGGTGGCCCACTCCTGTAATCCCCGCTACTCGAGAGGCTGAGACAAGAGAACTGTC T G FBXL20 Ensembl:ENSG00000108306 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1204756343 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183875,RMVar_hsa_circ_9121,RMVar_hsa_circ_316339,RMVar_hsa_circ_368707,RMVar_hsa_circ_306646,RMVar_hsa_circ_79903,RMVar_hsa_circ_266439,RMVar_hsa_circ_126683,RMVar_hsa_circ_183872,RMVar_hsa_circ_183873,RMVar_hsa_circ_183874,RMVar_hsa_circ_292083,RMVar_hsa_circ_19251,RMVar_hsa_circ_306827,RMVar_hsa_circ_40944,RMVar_hsa_circ_48133,RMVar_hsa_circ_183877,RMVar_hsa_circ_183878,RMVar_hsa_circ_183879,RMVar_hsa_circ_183876,RMVar_hsa_circ_26767,RMVar_hsa_circ_312569,RMVar_hsa_circ_328566,RMVar_hsa_circ_331569,RMVar_hsa_circ_313981,RMVar_hsa_circ_43842,RMVar_hsa_circ_183880 50358 RMVar_ID_50358 Human_SNP_ID_623808705 A-to-I Human chr17 - 39298555 39298555 39298555 CACCACGCCTGGCTAAGTTTTAAAATTTTTTTATAGAGTCAGGGTCTCATTTTGTTGTCCAGGCT CACCACGCCTGGCTAAGTTTTAAAATTTTTTTGTAGAGTCAGGGTCTCATTTTGTTGTCCAGGCT T C FBXL20 Ensembl:ENSG00000108306 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs964220323 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183875,RMVar_hsa_circ_316339,RMVar_hsa_circ_126683,RMVar_hsa_circ_183874,RMVar_hsa_circ_19251,RMVar_hsa_circ_26767,RMVar_hsa_circ_43842,RMVar_hsa_circ_66355,RMVar_hsa_circ_315313,RMVar_hsa_circ_277173,RMVar_hsa_circ_38425,RMVar_hsa_circ_42089,RMVar_hsa_circ_183884,RMVar_hsa_circ_183886,RMVar_hsa_circ_285405,RMVar_hsa_circ_183885,RMVar_hsa_circ_317737,RMVar_hsa_circ_341093,RMVar_hsa_circ_321488,RMVar_hsa_circ_333585,RMVar_hsa_circ_183888,RMVar_hsa_circ_281521,RMVar_hsa_circ_183887 50359 RMVar_ID_50359 Human_SNP_ID_623810682 A-to-I Human chr17 - 39306143 39306143 39306143 CCGTCTTAAAAAAAAAAAAAAGAACTCACTCTATCACCCAGGCTGGAGTACAGTGCTGTGATTGT CCGTCTTAAAAAAAAAAAAAAGAACTCACTCTGTCACCCAGGCTGGAGTACAGTGCTGTGATTGT T C FBXL20 Ensembl:ENSG00000108306 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1315682170 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19251,RMVar_hsa_circ_315313,RMVar_hsa_circ_285405,RMVar_hsa_circ_183885,RMVar_hsa_circ_317737,RMVar_hsa_circ_183888,RMVar_hsa_circ_183891,RMVar_hsa_circ_303994 50360 RMVar_ID_50360 Human_SNP_ID_623810683 A-to-I Human chr17 - 39306143 39306143 39306143 CCGTCTTAAAAAAAAAAAAAAGAACTCACTCTATCACCCAGGCTGGAGTACAGTGCTGTGATTGT CCGTCTTAAAAAAAAAAAAAAGAACTCACTCTCTCACCCAGGCTGGAGTACAGTGCTGTGATTGT T G FBXL20 Ensembl:ENSG00000108306 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1315682170 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19251,RMVar_hsa_circ_315313,RMVar_hsa_circ_285405,RMVar_hsa_circ_183885,RMVar_hsa_circ_317737,RMVar_hsa_circ_183888,RMVar_hsa_circ_183891,RMVar_hsa_circ_303994 50361 RMVar_ID_50361 Human_SNP_ID_623816662 A-to-I Human chr17 - 39326505 39326505 39326505 GTGATCCCCCCACCTCAGCCCTCCTAGTAGCTAGGATCACAGGTGGGTGCCACCACACCCAGCTA GTGATCCCCCCACCTCAGCCCTCCTAGTAGCTGGGATCACAGGTGGGTGCCACCACACCCAGCTA T C FBXL20 Ensembl:ENSG00000108306 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1002277891 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19251,RMVar_hsa_circ_315313,RMVar_hsa_circ_285405,RMVar_hsa_circ_183885,RMVar_hsa_circ_317737,RMVar_hsa_circ_183888,RMVar_hsa_circ_183891,RMVar_hsa_circ_303994 50362 RMVar_ID_50362 Human_SNP_ID_623816717 A-to-I Human chr17 - 39326712 39326712 39326712 GGGAGGTTGAGACGAGAGGATTGCTTGAGGCCAGGAGTTTGAGGCTGCAGTGAGGTATATGATAG GGGAGGTTGAGACGAGAGGATTGCTTGAGGCCGGGAGTTTGAGGCTGCAGTGAGGTATATGATAG T C FBXL20 Ensembl:ENSG00000108306 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1371956660 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19251,RMVar_hsa_circ_315313,RMVar_hsa_circ_285405,RMVar_hsa_circ_183885,RMVar_hsa_circ_317737,RMVar_hsa_circ_183888,RMVar_hsa_circ_183891,RMVar_hsa_circ_303994 50363 RMVar_ID_50363 Human_SNP_ID_623816718 A-to-I Human chr17 - 39326717 39326717 39326717 TACTTGGGAGGTTGAGACGAGAGGATTGCTTGAGGCCAGGAGTTTGAGGCTGCAGTGAGGTATAT TACTTGGGAGGTTGAGACGAGAGGATTGCTTGGGGCCAGGAGTTTGAGGCTGCAGTGAGGTATAT T C FBXL20 Ensembl:ENSG00000108306 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985147991 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19251,RMVar_hsa_circ_315313,RMVar_hsa_circ_285405,RMVar_hsa_circ_183885,RMVar_hsa_circ_317737,RMVar_hsa_circ_183888,RMVar_hsa_circ_183891,RMVar_hsa_circ_303994 50364 RMVar_ID_50364 Human_SNP_ID_623819602 A-to-I Human chr17 - 39336641 39336641 39336641 TTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTTGTCTCAAACTCCTCACCT TTTTGTATTTTTAGTAGAGATGGGGTTTCACCGTGTTGGCCAGGCTTGTCTCAAACTCCTCACCT T C FBXL20 Ensembl:ENSG00000108306 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335494224 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19251,RMVar_hsa_circ_315313,RMVar_hsa_circ_285405,RMVar_hsa_circ_183885,RMVar_hsa_circ_317737,RMVar_hsa_circ_183888,RMVar_hsa_circ_183891,RMVar_hsa_circ_303994 50365 RMVar_ID_50365 Human_SNP_ID_623820502 A-to-I Human chr17 - 39339001 39339001 39339001 ACCACACTTGGCTAGTTTTTGTATTTTTTGGTAGAGACAGGGATTCACGATGTTGGCCAGGCTGG ACCACACTTGGCTAGTTTTTGTATTTTTTGGTGGAGACAGGGATTCACGATGTTGGCCAGGCTGG T C FBXL20 Ensembl:ENSG00000108306 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1250349490 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19251,RMVar_hsa_circ_315313,RMVar_hsa_circ_285405,RMVar_hsa_circ_183885,RMVar_hsa_circ_317737,RMVar_hsa_circ_183888,RMVar_hsa_circ_183891,RMVar_hsa_circ_303994 50366 RMVar_ID_50366 Human_SNP_ID_623823211 A-to-I Human chr17 - 39348941 39348941 39348941 GGCCTAATCCCAGCAATTTGAGAGGCTGAGGCAGGAGGATCTGTTGAGCTCAGGCATTCAAGACT GGCCTAATCCCAGCAATTTGAGAGGCTGAGGCGGGAGGATCTGTTGAGCTCAGGCATTCAAGACT T C FBXL20 Ensembl:ENSG00000108306 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs907825881 Functional Loss SNV dbSNP153 33..33 33 - - - 50367 RMVar_ID_50367 Human_SNP_ID_623825426 A-to-I Human chr17 - 39356936 39356936 39356936 AATGGGGCTGGGTACGATAGCTCATGCCTGTAATCCCAGCACTTTGGGAGGTCAAAGTGGGAGGA AATGGGGCTGGGTACGATAGCTCATGCCTGTAGTCCCAGCACTTTGGGAGGTCAAAGTGGGAGGA T C FBXL20 Ensembl:ENSG00000108306 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1296083229 Functional Loss SNV dbSNP153 33..33 33 - - - 50368 RMVar_ID_50368 Human_SNP_ID_623827044 A-to-I Human chr17 - 39363094 39363094 39363094 GGGAGGGTGAGGCAGGAGAATCACTTGAACCCAGGAGGCGGAGGTTGTGATGAGCTGAGATCGCG GGGAGGGTGAGGCAGGAGAATCACTTGAACCCGGGAGGCGGAGGTTGTGATGAGCTGAGATCGCG T C FBXL20 Ensembl:ENSG00000108306 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956982981 Functional Loss SNV dbSNP153 33..33 33 - - - 50369 RMVar_ID_50369 Human_SNP_ID_623829271 A-to-I Human chr17 - 39370976 39370976 39370976 AAACTCAGGTGATCCACCCGCCTCAGCCTCCAAAAGTGCTGGGATTATAGGCGTGAGCCAACACC AAACTCAGGTGATCCACCCGCCTCAGCCTCCAGAAGTGCTGGGATTATAGGCGTGAGCCAACACC T C FBXL20 Ensembl:ENSG00000108306 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs369478198 Functional Loss SNV dbSNP153 33..33 33 - - - 50370 RMVar_ID_50370 Human_SNP_ID_623833431 A-to-I Human chr17 - 39385994 39385994 39385994 TTGAGACGGAATCTCTGTTGTCAGGCTGGAGTACAGTGGCGCGATCTTGGCTGACTGCAACCTCT TTGAGACGGAATCTCTGTTGTCAGGCTGGAGTGCAGTGGCGCGATCTTGGCTGACTGCAACCTCT T C FBXL20 Ensembl:ENSG00000108306 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1426080093 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1533001,Human_RBP_ID_12993053 50371 RMVar_ID_50371 Human_SNP_ID_623840800 A-to-I Human chr17 - 39411449 39411447 39411449 GCTGGCTAATTTTTTGTATTTTTAGTAGAGACAGGGTTTCACCCCGCTGGCCAGGCTGGTCTCAA GCTGGCTAATTTTTTGTATTTTTAGTAGAGAC__GGTTTCACCCCGCTGGCCAGGCTGGTCTCAA CCT C MED1 Ensembl:ENSG00000125686 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1159706534 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_104559,RMVar_hsa_circ_103193,RMVar_hsa_circ_183893,RMVar_hsa_circ_100808,RMVar_hsa_circ_183894,RMVar_hsa_circ_183896 50372 RMVar_ID_50372 Human_SNP_ID_623841197 A-to-I Human chr17 - 39412809 39412809 39412809 AATTTGCGGCCGGGTGCGGGGGTCACCCCTGTAATCCTAGCACTTTGGGAGGCTGAGGCGGGTAA AATTTGCGGCCGGGTGCGGGGGTCACCCCTGTTATCCTAGCACTTTGGGAGGCTGAGGCGGGTAA T A MED1 Ensembl:ENSG00000125686 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs753983990 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104559,RMVar_hsa_circ_103193,RMVar_hsa_circ_183893,RMVar_hsa_circ_100808,RMVar_hsa_circ_183894,RMVar_hsa_circ_183896 50373 RMVar_ID_50373 Human_SNP_ID_623841286 A-to-I Human chr17 - 39413215 39413215 39413215 TAAAAATTAGCCAGGTGTGGTGGCAGGTGCCTATAATCCCAGCTACTCAGGAGGCTGAGGCGGGA TAAAAATTAGCCAGGTGTGGTGGCAGGTGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCGGGA T C MED1 Ensembl:ENSG00000125686 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs933618928 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104559,RMVar_hsa_circ_103193,RMVar_hsa_circ_183893,RMVar_hsa_circ_100808,RMVar_hsa_circ_183894,RMVar_hsa_circ_183896 50374 RMVar_ID_50374 Human_SNP_ID_623842786 A-to-I Human chr17 - 39418519 39418519 39418519 GAGAGGCTTTTTTTTTTTTGAGACAGGGTCTCACTCTGTTGCCCAGACTGAACCACAGTGGCATG GAGAGGCTTTTTTTTTTTTGAGACAGGGTCTCTCTCTGTTGCCCAGACTGAACCACAGTGGCATG T A MED1 Ensembl:ENSG00000125686 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1472316378 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8805,RMVar_hsa_circ_104559,RMVar_hsa_circ_103193,RMVar_hsa_circ_183893,RMVar_hsa_circ_286668,RMVar_hsa_circ_100808,RMVar_hsa_circ_183894,RMVar_hsa_circ_372677,RMVar_hsa_circ_183896,RMVar_hsa_circ_343850,RMVar_hsa_circ_304738,RMVar_hsa_circ_80034,RMVar_hsa_circ_104912,RMVar_hsa_circ_15003,RMVar_hsa_circ_183904,RMVar_hsa_circ_183899,RMVar_hsa_circ_183901,RMVar_hsa_circ_183902,RMVar_hsa_circ_183903,RMVar_hsa_circ_183900,RMVar_hsa_circ_183898,RMVar_hsa_circ_116626 50375 RMVar_ID_50375 Human_SNP_ID_623844683 A-to-I Human chr17 - 39425253 39425253 39425253 CTGGGAGGTGGAGATTGCAGTGAGTCGAGATCACACCACTGCATTCCAGTCTGGACAGAGTGAGA CTGGGAGGTGGAGATTGCAGTGAGTCGAGATCGCACCACTGCATTCCAGTCTGGACAGAGTGAGA T C MED1 Ensembl:ENSG00000125686 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1182324454 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100808,RMVar_hsa_circ_372677,RMVar_hsa_circ_183896,RMVar_hsa_circ_304738,RMVar_hsa_circ_80034,RMVar_hsa_circ_104912,RMVar_hsa_circ_30905,RMVar_hsa_circ_183905,RMVar_hsa_circ_183901,RMVar_hsa_circ_183902,RMVar_hsa_circ_183903,RMVar_hsa_circ_183900,RMVar_hsa_circ_93336,RMVar_hsa_circ_278893,RMVar_hsa_circ_341094,RMVar_hsa_circ_367786,RMVar_hsa_circ_183906,RMVar_hsa_circ_183912,RMVar_hsa_circ_285321,RMVar_hsa_circ_350457,RMVar_hsa_circ_355926,RMVar_hsa_circ_363100,RMVar_hsa_circ_288204,RMVar_hsa_circ_22389,RMVar_hsa_circ_72013,RMVar_hsa_circ_183913,RMVar_hsa_circ_183914,RMVar_hsa_circ_365687,RMVar_hsa_circ_89106,RMVar_hsa_circ_183922,RMVar_hsa_circ_304532,RMVar_hsa_circ_183917,RMVar_hsa_circ_346431,RMVar_hsa_circ_375139,RMVar_hsa_circ_362157,RMVar_hsa_circ_315200,RMVar_hsa_circ_105952,RMVar_hsa_circ_285393,RMVar_hsa_circ_183923,RMVar_hsa_circ_183924,RMVar_hsa_circ_183918,RMVar_hsa_circ_183920,RMVar_hsa_circ_183921,RMVar_hsa_circ_183919 50376 RMVar_ID_50376 Human_SNP_ID_623844900 A-to-I Human chr17 - 39426073 39426073 39426073 GCTGGCGTACAGTGATTTGATCACAGCTCACTACAGCCCCCGAAGTCCTGGGCTCAAGCCATCCT GCTGGCGTACAGTGATTTGATCACAGCTCACTGCAGCCCCCGAAGTCCTGGGCTCAAGCCATCCT T C MED1 Ensembl:ENSG00000125686 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs766625257 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100808,RMVar_hsa_circ_372677,RMVar_hsa_circ_183896,RMVar_hsa_circ_304738,RMVar_hsa_circ_80034,RMVar_hsa_circ_104912,RMVar_hsa_circ_30905,RMVar_hsa_circ_183905,RMVar_hsa_circ_183901,RMVar_hsa_circ_183902,RMVar_hsa_circ_183903,RMVar_hsa_circ_183900,RMVar_hsa_circ_93336,RMVar_hsa_circ_278893,RMVar_hsa_circ_341094,RMVar_hsa_circ_367786,RMVar_hsa_circ_183906,RMVar_hsa_circ_183912,RMVar_hsa_circ_285321,RMVar_hsa_circ_350457,RMVar_hsa_circ_355926,RMVar_hsa_circ_363100,RMVar_hsa_circ_288204,RMVar_hsa_circ_22389,RMVar_hsa_circ_72013,RMVar_hsa_circ_183913,RMVar_hsa_circ_183914,RMVar_hsa_circ_365687,RMVar_hsa_circ_89106,RMVar_hsa_circ_183922,RMVar_hsa_circ_304532,RMVar_hsa_circ_183917,RMVar_hsa_circ_346431,RMVar_hsa_circ_375139,RMVar_hsa_circ_362157,RMVar_hsa_circ_315200,RMVar_hsa_circ_105952,RMVar_hsa_circ_285393,RMVar_hsa_circ_183923,RMVar_hsa_circ_183924,RMVar_hsa_circ_183918,RMVar_hsa_circ_183920,RMVar_hsa_circ_183921,RMVar_hsa_circ_183919 50377 RMVar_ID_50377 Human_SNP_ID_623847397 A-to-I Human chr17 - 39435839 39435839 39435839 AAATTAGCCGGGTGTGGTGGTGCTCGTCTGTAATTCCAGCTACACAGGAGGCTGAGGCTGGAGAA AAATTAGCCGGGTGTGGTGGTGCTCGTCTGTAGTTCCAGCTACACAGGAGGCTGAGGCTGGAGAA T C MED1 Ensembl:ENSG00000125686 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1338995851 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_80034,RMVar_hsa_circ_104912,RMVar_hsa_circ_6291,RMVar_hsa_circ_183902,RMVar_hsa_circ_183903,RMVar_hsa_circ_355926,RMVar_hsa_circ_22389,RMVar_hsa_circ_72013,RMVar_hsa_circ_183914,RMVar_hsa_circ_346431,RMVar_hsa_circ_362157,RMVar_hsa_circ_105952,RMVar_hsa_circ_75320,RMVar_hsa_circ_183918,RMVar_hsa_circ_183920,RMVar_hsa_circ_183919,RMVar_hsa_circ_352444,RMVar_hsa_circ_340831,RMVar_hsa_circ_285143,RMVar_hsa_circ_183928,RMVar_hsa_circ_183929,RMVar_hsa_circ_28956,RMVar_hsa_circ_265439,RMVar_hsa_circ_357079,RMVar_hsa_circ_70257,RMVar_hsa_circ_354246,RMVar_hsa_circ_359788,RMVar_hsa_circ_265531 50378 RMVar_ID_50378 Human_SNP_ID_623849273 A-to-I Human chr17 - 39442740 39442740 39442740 CCACCATGCCCGGGTAATTTTATATTTTTAGTAGAGACAGGGTTTTCCATGTTGGTCAGGCTGGT CCACCATGCCCGGGTAATTTTATATTTTTAGTGGAGACAGGGTTTTCCATGTTGGTCAGGCTGGT T C MED1 Ensembl:ENSG00000125686 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs934347418 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12993905 RMVar_hsa_circ_80034,RMVar_hsa_circ_183903,RMVar_hsa_circ_22389,RMVar_hsa_circ_72013,RMVar_hsa_circ_183914,RMVar_hsa_circ_105952,RMVar_hsa_circ_75320,RMVar_hsa_circ_183918,RMVar_hsa_circ_285143,RMVar_hsa_circ_183929,RMVar_hsa_circ_28956,RMVar_hsa_circ_357079,RMVar_hsa_circ_286315,RMVar_hsa_circ_354246,RMVar_hsa_circ_359788,RMVar_hsa_circ_183933,RMVar_hsa_circ_87572,RMVar_hsa_circ_183932,RMVar_hsa_circ_183935,RMVar_hsa_circ_183934,RMVar_hsa_circ_342581 50379 RMVar_ID_50379 Human_SNP_ID_623849275 A-to-I Human chr17 - 39442749 39442749 39442749 AGGCATGTGCCACCATGCCCGGGTAATTTTATATTTTTAGTAGAGACAGGGTTTTCCATGTTGGT AGGCATGTGCCACCATGCCCGGGTAATTTTATGTTTTTAGTAGAGACAGGGTTTTCCATGTTGGT T C MED1 Ensembl:ENSG00000125686 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1041076442 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12993906 RMVar_hsa_circ_80034,RMVar_hsa_circ_183903,RMVar_hsa_circ_22389,RMVar_hsa_circ_72013,RMVar_hsa_circ_183914,RMVar_hsa_circ_105952,RMVar_hsa_circ_75320,RMVar_hsa_circ_183918,RMVar_hsa_circ_285143,RMVar_hsa_circ_183929,RMVar_hsa_circ_28956,RMVar_hsa_circ_357079,RMVar_hsa_circ_286315,RMVar_hsa_circ_354246,RMVar_hsa_circ_359788,RMVar_hsa_circ_183933,RMVar_hsa_circ_87572,RMVar_hsa_circ_183932,RMVar_hsa_circ_183935,RMVar_hsa_circ_183934,RMVar_hsa_circ_342581 50380 RMVar_ID_50380 Human_SNP_ID_623855553 A-to-I Human chr17 + 39465586 39465585 39465586 TCGGTTCACTGCAACCTCTGCCTCTCGGGTTCAAGCTATTCTCCTGCCTCAGCCTCCTGAGAGTA TCGGTTCACTGCAACCTCTGCCTCTCGGGTTC_AGCTATTCTCCTGCCTCAGCCTCCTGAGAGTA CA C CDK12 Ensembl:ENSG00000167258 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs755884050 Functional Loss DEL dbSNP153 33..33 33 - - - 50381 RMVar_ID_50381 Human_SNP_ID_623855556 A-to-I Human chr17 + 39465586 39465586 39465586 TCGGTTCACTGCAACCTCTGCCTCTCGGGTTCAAGCTATTCTCCTGCCTCAGCCTCCTGAGAGTA TCGGTTCACTGCAACCTCTGCCTCTCGGGTTCCAGCTATTCTCCTGCCTCAGCCTCCTGAGAGTA A C CDK12 Ensembl:ENSG00000167258 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs535528785 Functional Loss SNV dbSNP153 33..33 33 - - - 50382 RMVar_ID_50382 Human_SNP_ID_623855557 A-to-I Human chr17 + 39465586 39465586 39465586 TCGGTTCACTGCAACCTCTGCCTCTCGGGTTCAAGCTATTCTCCTGCCTCAGCCTCCTGAGAGTA TCGGTTCACTGCAACCTCTGCCTCTCGGGTTCGAGCTATTCTCCTGCCTCAGCCTCCTGAGAGTA A G CDK12 Ensembl:ENSG00000167258 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs535528785 Functional Loss SNV dbSNP153 33..33 33 - - - 50383 RMVar_ID_50383 Human_SNP_ID_623856117 A-to-I Human chr17 + 39467251 39467251 39467251 TGCCTGCCTCAGCCTCCCAAAGCGCTGGGATTACAGGCATGAGCCACCATGCCCGGCGAAACAAC TGCCTGCCTCAGCCTCCCAAAGCGCTGGGATTGCAGGCATGAGCCACCATGCCCGGCGAAACAAC A G CDK12 Ensembl:ENSG00000167258 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs925604007 Functional Loss SNV dbSNP153 33..33 33 - - - 50384 RMVar_ID_50384 Human_SNP_ID_623857658 A-to-I Human chr17 + 39472563 39472563 39472563 GGGCGTGGTGGTGGGCCCCTGTAATCCCAGCTACTTGAGAGGCTGAGGCAGGAGAATTGCTTGAA GGGCGTGGTGGTGGGCCCCTGTAATCCCAGCTGCTTGAGAGGCTGAGGCAGGAGAATTGCTTGAA A G CDK12 Ensembl:ENSG00000167258 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1044467174 Functional Loss SNV dbSNP153 33..33 33 - - - 50385 RMVar_ID_50385 Human_SNP_ID_623858651 A-to-I Human chr17 + 39476345 39476345 39476345 TTTCTCCTGGATGGTCTCGATGTCTTGATCTCATGATCTGTCCGCCTCAGCCTCCCAAAGTACTG TTTCTCCTGGATGGTCTCGATGTCTTGATCTCCTGATCTGTCCGCCTCAGCCTCCCAAAGTACTG A C CDK12 Ensembl:ENSG00000167258 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs868591306 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8451445,Human_RBP_ID_12994231 50386 RMVar_ID_50386 Human_SNP_ID_623858710 A-to-I Human chr17 + 39476513 39476513 39476513 TGTGATCTCGGCTGCATCCGCCTCCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGC TGTGATCTCGGCTGCATCCGCCTCCCGGGTTCGAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGC A G CDK12 Ensembl:ENSG00000167258 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1469855858 Functional Loss SNV dbSNP153 33..33 33 - - - 50387 RMVar_ID_50387 Human_SNP_ID_623859337 A-to-I Human chr17 + 39478374 39478374 39478374 CCACCATATCCGGATAATTTTTTTGTATTTTTAGTAGAGACAGGGTTTCATCATGTCATCCAGGC CCACCATATCCGGATAATTTTTTTGTATTTTTCGTAGAGACAGGGTTTCATCATGTCATCCAGGC A C CDK12 Ensembl:ENSG00000167258 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1006188387 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12994289 50388 RMVar_ID_50388 Human_SNP_ID_623859964 A-to-I Human chr17 + 39480497 39480497 39480497 GAGAGTTTTGCTAGTTGCCCAGGCTGGAGTGCAATGGTGCGATCTCAGCTCACTGCAACCTCTGC GAGAGTTTTGCTAGTTGCCCAGGCTGGAGTGCGATGGTGCGATCTCAGCTCACTGCAACCTCTGC A G CDK12 Ensembl:ENSG00000167258 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1409472637 Functional Loss SNV dbSNP153 33..33 33 - - - 50389 RMVar_ID_50389 Human_SNP_ID_623860730 A-to-I Human chr17 + 39482280 39482280 39482280 GTGATCCACCCGCCTCGGCCTCTCAGAGTGCTAGGATTACAGGCCTGAGCTACCGCACCTGGCCT GTGATCCACCCGCCTCGGCCTCTCAGAGTGCTGGGATTACAGGCCTGAGCTACCGCACCTGGCCT A G CDK12 Ensembl:ENSG00000167258 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1254798858 Functional Loss SNV dbSNP153 33..33 33 - - - 50390 RMVar_ID_50390 Human_SNP_ID_623861867 A-to-I Human chr17 + 39486213 39486213 39486213 GACTTCAGGTGATCCGCCCGCTTGGCCTCCCAAAGTGCTGGGATTACAGACATGAGCCACTGCAC GACTTCAGGTGATCCGCCCGCTTGGCCTCCCAGAGTGCTGGGATTACAGACATGAGCCACTGCAC A G CDK12 Ensembl:ENSG00000167258 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1190751033 Functional Loss SNV dbSNP153 33..33 33 - - - 50391 RMVar_ID_50391 Human_SNP_ID_623862294 A-to-I Human chr17 + 39487696 39487696 39487696 TGGAGTGCAGTGGCACGATCTCGGCTTACTGCAACCTTGACCTCCCCAGTTCAAGCAATTCTCAT TGGAGTGCAGTGGCACGATCTCGGCTTACTGCCACCTTGACCTCCCCAGTTCAAGCAATTCTCAT A C CDK12 Ensembl:ENSG00000167258 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971962673 Functional Loss SNV dbSNP153 33..33 33 - - - 50392 RMVar_ID_50392 Human_SNP_ID_623863889 A-to-I Human chr17 + 39493192 39493191 39493193 ATTTTTGTTTTTTTTTTTTTTTTAGTAGAAACAGGGTTCCACTATGTCGTCCAGGCTGGTCTTGA ATTTTTGTTTTTTTTTTTTTTTTAGTAGAAAC__GGTTCCACTATGTCGTCCAGGCTGGTCTTGA CAG C CDK12 Ensembl:ENSG00000167258 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1214445024 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_183939,RMVar_hsa_circ_293013,RMVar_hsa_circ_319551,RMVar_hsa_circ_321857,RMVar_hsa_circ_356019,RMVar_hsa_circ_316433,RMVar_hsa_circ_303307,RMVar_hsa_circ_45488,RMVar_hsa_circ_273942,RMVar_hsa_circ_75854,RMVar_hsa_circ_183941,RMVar_hsa_circ_183942,RMVar_hsa_circ_183940,RMVar_hsa_circ_183937,RMVar_hsa_circ_183938,RMVar_hsa_circ_109991,RMVar_hsa_circ_365481,RMVar_hsa_circ_183945 50393 RMVar_ID_50393 Human_SNP_ID_623863891 A-to-I Human chr17 + 39493192 39493192 39493192 ATTTTTGTTTTTTTTTTTTTTTTAGTAGAAACAGGGTTCCACTATGTCGTCCAGGCTGGTCTTGA ATTTTTGTTTTTTTTTTTTTTTTAGTAGAAACGGGGTTCCACTATGTCGTCCAGGCTGGTCTTGA A G CDK12 Ensembl:ENSG00000167258 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1299373214 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183939,RMVar_hsa_circ_293013,RMVar_hsa_circ_319551,RMVar_hsa_circ_321857,RMVar_hsa_circ_356019,RMVar_hsa_circ_316433,RMVar_hsa_circ_303307,RMVar_hsa_circ_45488,RMVar_hsa_circ_273942,RMVar_hsa_circ_75854,RMVar_hsa_circ_183941,RMVar_hsa_circ_183942,RMVar_hsa_circ_183940,RMVar_hsa_circ_183937,RMVar_hsa_circ_183938,RMVar_hsa_circ_109991,RMVar_hsa_circ_365481,RMVar_hsa_circ_183945 50394 RMVar_ID_50394 Human_SNP_ID_623864050 A-to-I Human chr17 + 39493885 39493885 39493885 AGGCGTGGTGCCACACGCCTGTAGTCCCAGCTACTCAGGAGGCGGAGGCAGGAGAATCACTTGAA AGGCGTGGTGCCACACGCCTGTAGTCCCAGCTCCTCAGGAGGCGGAGGCAGGAGAATCACTTGAA A C CDK12 Ensembl:ENSG00000167258 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1249775814 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183939,RMVar_hsa_circ_293013,RMVar_hsa_circ_319551,RMVar_hsa_circ_321857,RMVar_hsa_circ_356019,RMVar_hsa_circ_316433,RMVar_hsa_circ_303307,RMVar_hsa_circ_45488,RMVar_hsa_circ_273942,RMVar_hsa_circ_75854,RMVar_hsa_circ_183941,RMVar_hsa_circ_183942,RMVar_hsa_circ_183940,RMVar_hsa_circ_183937,RMVar_hsa_circ_183938,RMVar_hsa_circ_109991,RMVar_hsa_circ_365481,RMVar_hsa_circ_183945 50395 RMVar_ID_50395 Human_SNP_ID_623864153 A-to-I Human chr17 + 39494177 39494177 39494177 CTCACCGCAACCTCTGCCTCCCGGGTTCAAGCAATTCTCCTGTCTCAGCCTCCTGAGTAGCTGGG CTCACCGCAACCTCTGCCTCCCGGGTTCAAGCGATTCTCCTGTCTCAGCCTCCTGAGTAGCTGGG A G CDK12 Ensembl:ENSG00000167258 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1479575002 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183939,RMVar_hsa_circ_293013,RMVar_hsa_circ_319551,RMVar_hsa_circ_321857,RMVar_hsa_circ_356019,RMVar_hsa_circ_316433,RMVar_hsa_circ_303307,RMVar_hsa_circ_45488,RMVar_hsa_circ_273942,RMVar_hsa_circ_75854,RMVar_hsa_circ_183941,RMVar_hsa_circ_183942,RMVar_hsa_circ_183940,RMVar_hsa_circ_183937,RMVar_hsa_circ_183938,RMVar_hsa_circ_109991,RMVar_hsa_circ_365481,RMVar_hsa_circ_183945 50396 RMVar_ID_50396 Human_SNP_ID_623864166 A-to-I Human chr17 + 39494253 39494253 39494253 CCACCACCACGCCCAGCTAATTTTTGTATTTTAATAGAGACGGGGTTTCACCACGTTGGCTAGGC CCACCACCACGCCCAGCTAATTTTTGTATTTTGATAGAGACGGGGTTTCACCACGTTGGCTAGGC A G CDK12 Ensembl:ENSG00000167258 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1423250315 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183939,RMVar_hsa_circ_293013,RMVar_hsa_circ_319551,RMVar_hsa_circ_321857,RMVar_hsa_circ_356019,RMVar_hsa_circ_316433,RMVar_hsa_circ_303307,RMVar_hsa_circ_45488,RMVar_hsa_circ_273942,RMVar_hsa_circ_75854,RMVar_hsa_circ_183941,RMVar_hsa_circ_183942,RMVar_hsa_circ_183940,RMVar_hsa_circ_183937,RMVar_hsa_circ_183938,RMVar_hsa_circ_109991,RMVar_hsa_circ_365481,RMVar_hsa_circ_183945 50397 RMVar_ID_50397 Human_SNP_ID_623864813 A-to-I Human chr17 + 39496444 39496444 39496444 ATAATAGGCCAGGTGCAGTGGCTCACCCCTGTAATCTCAGCACTTTGGGAGGCCGAGTCAGGTTG ATAATAGGCCAGGTGCAGTGGCTCACCCCTGTCATCTCAGCACTTTGGGAGGCCGAGTCAGGTTG A C CDK12 Ensembl:ENSG00000167258 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs971402628 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183939,RMVar_hsa_circ_319551,RMVar_hsa_circ_321857,RMVar_hsa_circ_356019,RMVar_hsa_circ_316433,RMVar_hsa_circ_303307,RMVar_hsa_circ_45488,RMVar_hsa_circ_273942,RMVar_hsa_circ_75854,RMVar_hsa_circ_183941,RMVar_hsa_circ_183940,RMVar_hsa_circ_183937,RMVar_hsa_circ_183938,RMVar_hsa_circ_109991,RMVar_hsa_circ_72694,RMVar_hsa_circ_183945 50398 RMVar_ID_50398 Human_SNP_ID_623864833 A-to-I Human chr17 + 39496529 39496529 39496529 TGAGATCAGCCTGGCCAAGATGGTGAAACCCTATCTCTACTAAAAATACAATAATTAGCTGGGCA TGAGATCAGCCTGGCCAAGATGGTGAAACCCTGTCTCTACTAAAAATACAATAATTAGCTGGGCA A G CDK12 Ensembl:ENSG00000167258 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs989013899 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183939,RMVar_hsa_circ_319551,RMVar_hsa_circ_321857,RMVar_hsa_circ_356019,RMVar_hsa_circ_316433,RMVar_hsa_circ_303307,RMVar_hsa_circ_45488,RMVar_hsa_circ_273942,RMVar_hsa_circ_75854,RMVar_hsa_circ_183941,RMVar_hsa_circ_183940,RMVar_hsa_circ_183937,RMVar_hsa_circ_183938,RMVar_hsa_circ_109991,RMVar_hsa_circ_72694,RMVar_hsa_circ_183945 50399 RMVar_ID_50399 Human_SNP_ID_623864844 A-to-I Human chr17 + 39496579 39496579 39496579 ATAATTAGCTGGGCATGGTGGCTAGCGCCTGTAATCTTCAGCTACTTGGGAGGCTGAGGCAGGAG ATAATTAGCTGGGCATGGTGGCTAGCGCCTGTCATCTTCAGCTACTTGGGAGGCTGAGGCAGGAG A C CDK12 Ensembl:ENSG00000167258 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs942354835 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25280282 RMVar_hsa_circ_183939,RMVar_hsa_circ_319551,RMVar_hsa_circ_321857,RMVar_hsa_circ_356019,RMVar_hsa_circ_316433,RMVar_hsa_circ_303307,RMVar_hsa_circ_45488,RMVar_hsa_circ_273942,RMVar_hsa_circ_75854,RMVar_hsa_circ_183941,RMVar_hsa_circ_183940,RMVar_hsa_circ_183937,RMVar_hsa_circ_183938,RMVar_hsa_circ_109991,RMVar_hsa_circ_72694,RMVar_hsa_circ_183945 50400 RMVar_ID_50400 Human_SNP_ID_623864847 A-to-I Human chr17 + 39496590 39496590 39496590 GGCATGGTGGCTAGCGCCTGTAATCTTCAGCTACTTGGGAGGCTGAGGCAGGAGAATGACTTGAA GGCATGGTGGCTAGCGCCTGTAATCTTCAGCTGCTTGGGAGGCTGAGGCAGGAGAATGACTTGAA A G CDK12 Ensembl:ENSG00000167258 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs187646182 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183939,RMVar_hsa_circ_319551,RMVar_hsa_circ_321857,RMVar_hsa_circ_356019,RMVar_hsa_circ_316433,RMVar_hsa_circ_303307,RMVar_hsa_circ_45488,RMVar_hsa_circ_273942,RMVar_hsa_circ_75854,RMVar_hsa_circ_183941,RMVar_hsa_circ_183940,RMVar_hsa_circ_183937,RMVar_hsa_circ_183938,RMVar_hsa_circ_109991,RMVar_hsa_circ_72694,RMVar_hsa_circ_183945 50401 RMVar_ID_50401 Human_SNP_ID_623865001 A-to-I Human chr17 + 39497098 39497098 39497098 GCTTAAACAGGCGCACGCCACCACGGCCGGCTAATTTTTGTATCTTTATCAGAGACAGGGTTTCG GCTTAAACAGGCGCACGCCACCACGGCCGGCTCATTTTTGTATCTTTATCAGAGACAGGGTTTCG A C CDK12 Ensembl:ENSG00000167258 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1329241686 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183939,RMVar_hsa_circ_319551,RMVar_hsa_circ_321857,RMVar_hsa_circ_356019,RMVar_hsa_circ_316433,RMVar_hsa_circ_303307,RMVar_hsa_circ_45488,RMVar_hsa_circ_273942,RMVar_hsa_circ_75854,RMVar_hsa_circ_183941,RMVar_hsa_circ_183940,RMVar_hsa_circ_183937,RMVar_hsa_circ_183938,RMVar_hsa_circ_109991,RMVar_hsa_circ_72694,RMVar_hsa_circ_183945 50402 RMVar_ID_50402 Human_SNP_ID_623866315 A-to-I Human chr17 + 39499697 39499697 39499697 ATGCCTGGCTAATTTTTGTATTTTTTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGTTGG ATGCCTGGCTAATTTTTGTATTTTTTTTTAGTGGAGATGGGGTTTCACCATGTTGGCCAGGTTGG A G CDK12 Ensembl:ENSG00000167258 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1459094070 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183939,RMVar_hsa_circ_319551,RMVar_hsa_circ_321857,RMVar_hsa_circ_356019,RMVar_hsa_circ_316433,RMVar_hsa_circ_303307,RMVar_hsa_circ_45488,RMVar_hsa_circ_273942,RMVar_hsa_circ_75854,RMVar_hsa_circ_183941,RMVar_hsa_circ_183940,RMVar_hsa_circ_183937,RMVar_hsa_circ_183938,RMVar_hsa_circ_109991,RMVar_hsa_circ_72694,RMVar_hsa_circ_183945 50403 RMVar_ID_50403 Human_SNP_ID_623866622 A-to-I Human chr17 + 39501012 39501012 39501012 CCCTCCTCGGCCTCCCAAAGTGCTGGGGTTACAGGCATCAGCCACTGCGCCCAGCCACAGAAGAT CCCTCCTCGGCCTCCCAAAGTGCTGGGGTTACTGGCATCAGCCACTGCGCCCAGCCACAGAAGAT A T CDK12 Ensembl:ENSG00000167258 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs929124381 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183939,RMVar_hsa_circ_319551,RMVar_hsa_circ_321857,RMVar_hsa_circ_356019,RMVar_hsa_circ_316433,RMVar_hsa_circ_303307,RMVar_hsa_circ_45488,RMVar_hsa_circ_273942,RMVar_hsa_circ_75854,RMVar_hsa_circ_183941,RMVar_hsa_circ_183940,RMVar_hsa_circ_183937,RMVar_hsa_circ_183938,RMVar_hsa_circ_109991,RMVar_hsa_circ_72694,RMVar_hsa_circ_183945 50404 RMVar_ID_50404 Human_SNP_ID_623866623 A-to-I Human chr17 + 39501016 39501016 39501016 CCTCGGCCTCCCAAAGTGCTGGGGTTACAGGCATCAGCCACTGCGCCCAGCCACAGAAGATTAAT CCTCGGCCTCCCAAAGTGCTGGGGTTACAGGCGTCAGCCACTGCGCCCAGCCACAGAAGATTAAT A G CDK12 Ensembl:ENSG00000167258 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs992589687 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183939,RMVar_hsa_circ_319551,RMVar_hsa_circ_321857,RMVar_hsa_circ_356019,RMVar_hsa_circ_316433,RMVar_hsa_circ_303307,RMVar_hsa_circ_45488,RMVar_hsa_circ_273942,RMVar_hsa_circ_75854,RMVar_hsa_circ_183941,RMVar_hsa_circ_183940,RMVar_hsa_circ_183937,RMVar_hsa_circ_183938,RMVar_hsa_circ_109991,RMVar_hsa_circ_72694,RMVar_hsa_circ_183945 50405 RMVar_ID_50405 Human_SNP_ID_623867163 A-to-I Human chr17 + 39502994 39502994 39502994 AACTTTATCTGTATTTGACAGGGATCAGCATCACTTGAACCCAGGAGGTAGAGGTTACAGTGAGC AACTTTATCTGTATTTGACAGGGATCAGCATCGCTTGAACCCAGGAGGTAGAGGTTACAGTGAGC A G CDK12 Ensembl:ENSG00000167258 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs561150739 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12994676 RMVar_hsa_circ_183939,RMVar_hsa_circ_319551,RMVar_hsa_circ_321857,RMVar_hsa_circ_356019,RMVar_hsa_circ_316433,RMVar_hsa_circ_303307,RMVar_hsa_circ_45488,RMVar_hsa_circ_75854,RMVar_hsa_circ_183940,RMVar_hsa_circ_183937,RMVar_hsa_circ_183938,RMVar_hsa_circ_109991,RMVar_hsa_circ_183945,RMVar_hsa_circ_14856 50406 RMVar_ID_50406 Human_SNP_ID_623867538 A-to-I Human chr17 + 39504727 39504705 39504727 ATAGCAAAATTCTGTCTCTACTAAAAGTACAAAAATTAGCTGAGCTTGGTGGTGCACGCATCTAA ATAGCAAAATT______________________AATTAGCTGAGCTTGGTGGTGCACGCATCTAA TCTGTCTCTACTAAAAGTACAAA T CDK12 Ensembl:ENSG00000167258 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1360863245 Functional Loss DEL dbSNP153 12..33 33 - - - Human_RBP_ID_18696627 RMVar_hsa_circ_183939,RMVar_hsa_circ_319551,RMVar_hsa_circ_321857,RMVar_hsa_circ_356019,RMVar_hsa_circ_316433,RMVar_hsa_circ_303307,RMVar_hsa_circ_45488,RMVar_hsa_circ_75854,RMVar_hsa_circ_183940,RMVar_hsa_circ_183937,RMVar_hsa_circ_183938,RMVar_hsa_circ_109991,RMVar_hsa_circ_183945,RMVar_hsa_circ_14856 50407 RMVar_ID_50407 Human_SNP_ID_623868594 A-to-I Human chr17 + 39508813 39508813 39508813 GCACAGGAATTTAAGACCAGCCTAGGCAACATAGGGGAACTCTGTCTCTACAAAAAATAAAATAA GCACAGGAATTTAAGACCAGCCTAGGCAACATGGGGGAACTCTGTCTCTACAAAAAATAAAATAA A G CDK12 Ensembl:ENSG00000167258 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1196748285 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12994721 RMVar_hsa_circ_183939,RMVar_hsa_circ_319551,RMVar_hsa_circ_321857,RMVar_hsa_circ_356019,RMVar_hsa_circ_316433,RMVar_hsa_circ_303307,RMVar_hsa_circ_45488,RMVar_hsa_circ_75854,RMVar_hsa_circ_183940,RMVar_hsa_circ_183937,RMVar_hsa_circ_183938,RMVar_hsa_circ_109991,RMVar_hsa_circ_183945,RMVar_hsa_circ_14856 50408 RMVar_ID_50408 Human_SNP_ID_623869142 A-to-I Human chr17 + 39510813 39510813 39510813 TTTTGTATTTTTAGTGGAGATGGGGTTTCTCCATGTTGGTCACGCTGGTCTCGAACTCCCGACCT TTTTGTATTTTTAGTGGAGATGGGGTTTCTCCGTGTTGGTCACGCTGGTCTCGAACTCCCGACCT A G CDK12 Ensembl:ENSG00000167258 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs560362083 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183939,RMVar_hsa_circ_321857,RMVar_hsa_circ_356019,RMVar_hsa_circ_316433,RMVar_hsa_circ_303307,RMVar_hsa_circ_45488,RMVar_hsa_circ_75854,RMVar_hsa_circ_183937,RMVar_hsa_circ_183938,RMVar_hsa_circ_109991,RMVar_hsa_circ_183945,RMVar_hsa_circ_14856,RMVar_hsa_circ_352203 50409 RMVar_ID_50409 Human_SNP_ID_623869143 A-to-I Human chr17 + 39510813 39510813 39510813 TTTTGTATTTTTAGTGGAGATGGGGTTTCTCCATGTTGGTCACGCTGGTCTCGAACTCCCGACCT TTTTGTATTTTTAGTGGAGATGGGGTTTCTCCTTGTTGGTCACGCTGGTCTCGAACTCCCGACCT A T CDK12 Ensembl:ENSG00000167258 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs560362083 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_183939,RMVar_hsa_circ_321857,RMVar_hsa_circ_356019,RMVar_hsa_circ_316433,RMVar_hsa_circ_303307,RMVar_hsa_circ_45488,RMVar_hsa_circ_75854,RMVar_hsa_circ_183937,RMVar_hsa_circ_183938,RMVar_hsa_circ_109991,RMVar_hsa_circ_183945,RMVar_hsa_circ_14856,RMVar_hsa_circ_352203 50410 RMVar_ID_50410 Human_SNP_ID_623871526 A-to-I Human chr17 + 39520520 39520520 39520520 TCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGACACACACCACCACACCCA TCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTGGCTGGGACTACAGACACACACCACCACACCCA A G CDK12 Ensembl:ENSG00000167258 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1355076783 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_316433,RMVar_hsa_circ_45488,RMVar_hsa_circ_183937,RMVar_hsa_circ_75769,RMVar_hsa_circ_113972,RMVar_hsa_circ_328940,RMVar_hsa_circ_183948,RMVar_hsa_circ_183949 50411 RMVar_ID_50411 Human_SNP_ID_623872084 A-to-I Human chr17 + 39522614 39522614 39522614 CGGCACCACAGCTGGCTAATTTTTGTATTTTTAGTAGAGATGAGGTTTCACCATGTTGACCAGAC CGGCACCACAGCTGGCTAATTTTTGTATTTTTGGTAGAGATGAGGTTTCACCATGTTGACCAGAC A G CDK12 Ensembl:ENSG00000167258 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1298045410 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_316433,RMVar_hsa_circ_45488,RMVar_hsa_circ_183937,RMVar_hsa_circ_75769,RMVar_hsa_circ_113972,RMVar_hsa_circ_328940,RMVar_hsa_circ_183948,RMVar_hsa_circ_183949 50412 RMVar_ID_50412 Human_SNP_ID_623872155 A-to-I Human chr17 + 39522890 39522890 39522890 CCTGGCCAACATGGTAAAACCCCGTCTCTCCTAAAAATACAAAAAATTAACCAGGTGTGGTGGTG CCTGGCCAACATGGTAAAACCCCGTCTCTCCTGAAAATACAAAAAATTAACCAGGTGTGGTGGTG A G CDK12 Ensembl:ENSG00000167258 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1466081019 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_316433,RMVar_hsa_circ_45488,RMVar_hsa_circ_183937,RMVar_hsa_circ_75769,RMVar_hsa_circ_113972,RMVar_hsa_circ_328940,RMVar_hsa_circ_183948,RMVar_hsa_circ_183949 50413 RMVar_ID_50413 Human_SNP_ID_623880514 A-to-I Human chr17 + 39559643 39559643 39559643 ACAGGATCTTGCTCTGTCACCCAGAATGGAGTACAGTGTCTCAATCATAGTTCACTGCAGCCTTG ACAGGATCTTGCTCTGTCACCCAGAATGGAGTGCAGTGTCTCAATCATAGTTCACTGCAGCCTTG A G CDK12 Ensembl:ENSG00000167258 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1137644 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12995343 RMVar_hsa_circ_183951 50414 RMVar_ID_50414 Human_SNP_ID_623901851 A-to-I Human chr17 + 39645525 39645525 39645525 AGAGTCTCACTGTGTCACCCGGGCGGGGGTGCAATGGTGTGATCTCGGCTCACTGCAACCTCCGC AGAGTCTCACTGTGTCACCCGGGCGGGGGTGCGATGGTGTGATCTCGGCTCACTGCAACCTCCGC A G STARD3 Ensembl:ENSG00000131748 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs967777273 Functional Loss SNV dbSNP153 33..33 33 - - - 50415 RMVar_ID_50415 Human_SNP_ID_623902266 A-to-I Human chr17 + 39647078 39647078 39647078 ATAAATAGGCAGGCGTGGTGGCGGGCACCTGTAGTCCCCTCTACTTGGGAGGCTGAGGCAGGAGA ATAAATAGGCAGGCGTGGTGGCGGGCACCTGTGGTCCCCTCTACTTGGGAGGCTGAGGCAGGAGA A G STARD3 Ensembl:ENSG00000131748 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1471459324 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_133383 50416 RMVar_ID_50416 Human_SNP_ID_623922753 A-to-I Human chr17 + 39722118 39722118 39722118 TTTTGTATTTTTAGTAGAGACGGGGTTTCTCCATGTTAGTCAGGCTGGTCTCGAACTCGAGAGCT TTTTGTATTTTTAGTAGAGACGGGGTTTCTCCGTGTTAGTCAGGCTGGTCTCGAACTCGAGAGCT A G ERBB2 Ensembl:ENSG00000141736 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs995416884 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76121,RMVar_hsa_circ_183962,RMVar_hsa_circ_79779,RMVar_hsa_circ_183969 50417 RMVar_ID_50417 Human_SNP_ID_623933181 A-to-I Human chr17 - 39760929 39760929 39760929 CCAGGCTAGTCTCAAAATCCTGGGCTCAAGCAATCTGCCCACCTCAGCCTCCCAAAGTGCTGGAA CCAGGCTAGTCTCAAAATCCTGGGCTCAAGCAGTCTGCCCACCTCAGCCTCCCAAAGTGCTGGAA T C IKZF3 Ensembl:ENSG00000161405 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs537966462 Functional Loss SNV dbSNP153 33..33 33 - - - 50418 RMVar_ID_50418 Human_SNP_ID_623933212 A-to-I Human chr17 - 39761077 39761077 39761077 AGATATAAAATGACCTCAGATTTTGATCTCCTAGGCTCAAACAATCCTCCTACCTCAGCCTCCCA AGATATAAAATGACCTCAGATTTTGATCTCCTGGGCTCAAACAATCCTCCTACCTCAGCCTCCCA T C IKZF3 Ensembl:ENSG00000161405 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1221965720 Functional Loss SNV dbSNP153 33..33 33 - - - 50419 RMVar_ID_50419 Human_SNP_ID_623933561 A-to-I Human chr17 - 39762624 39762624 39762624 CCTTGGCCTCCCACAGTGCTGGGATTACAGGCATGAGCTACCGCACCCAGCCTGAGACCACCTTT CCTTGGCCTCCCACAGTGCTGGGATTACAGGCGTGAGCTACCGCACCCAGCCTGAGACCACCTTT T C IKZF3 Ensembl:ENSG00000161405 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1257534623 Functional Loss SNV dbSNP153 33..33 33 - - - 50420 RMVar_ID_50420 Human_SNP_ID_623933617 A-to-I Human chr17 - 39762881 39762881 39762881 CCAACTTTTTTTGTTTTCTTTTGTTTTGAGACAGTCTCTCGCTCTGTTGCCCAGGCTGGAGTGCA CCAACTTTTTTTGTTTTCTTTTGTTTTGAGACGGTCTCTCGCTCTGTTGCCCAGGCTGGAGTGCA T C IKZF3 Ensembl:ENSG00000161405 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1440922870 Functional Loss SNV dbSNP153 33..33 33 - - - 50421 RMVar_ID_50421 Human_SNP_ID_623933855 A-to-I Human chr17 - 39764008 39764008 39764008 TCTACTAAAAATACAAAAATTAGCTGGGCAGTAGTGGCACATGCCTGTAATCCCAGCTACTCCGG TCTACTAAAAATACAAAAATTAGCTGGGCAGTGGTGGCACATGCCTGTAATCCCAGCTACTCCGG T C IKZF3 Ensembl:ENSG00000161405 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs954116662 Functional Loss SNV dbSNP153 33..33 33 - - - 50422 RMVar_ID_50422 Human_SNP_ID_623933886 A-to-I Human chr17 - 39764127 39764127 39764127 TTTCCGGCCAGGCTCGGTGGCTCACACCTGTAATCCCAACACTTTGGGAAGCCGAGGCAGGCGCA TTTCCGGCCAGGCTCGGTGGCTCACACCTGTAGTCCCAACACTTTGGGAAGCCGAGGCAGGCGCA T C IKZF3 Ensembl:ENSG00000161405 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs917398731 Functional Loss SNV dbSNP153 33..33 33 - - - 50423 RMVar_ID_50423 Human_SNP_ID_623937422 A-to-I Human chr17 - 39780765 39780765 39780765 CCAAGCTGAACTTGAACTCCTAGGCTCAAGCCATCCTCTCACCTCAGCCTCCTGAGTAGCTGGGA CCAAGCTGAACTTGAACTCCTAGGCTCAAGCCGTCCTCTCACCTCAGCCTCCTGAGTAGCTGGGA T C IKZF3 Ensembl:ENSG00000161405 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs937540256 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24956,RMVar_hsa_circ_57938 50424 RMVar_ID_50424 Human_SNP_ID_623954588 A-to-I Human chr17 - 39857729 39857728 39857729 ATAAATTAATGAATGAGTTGCCTGTGTGTTTGATCATTTGACTCTTTTCTTGCCCAGCTTTTATA ATAAATTAATGAATGAGTTGCCTGTGTGTTTG_TCATTTGACTCTTTTCTTGCCCAGCTTTTATA AT A IKZF3 Ensembl:ENSG00000161405 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1255962008 Functional Loss DEL dbSNP153 33..33 33 - - - 50425 RMVar_ID_50425 Human_SNP_ID_623954589 A-to-I Human chr17 - 39857729 39857729 39857729 ATAAATTAATGAATGAGTTGCCTGTGTGTTTGATCATTTGACTCTTTTCTTGCCCAGCTTTTATA ATAAATTAATGAATGAGTTGCCTGTGTGTTTGGTCATTTGACTCTTTTCTTGCCCAGCTTTTATA T C IKZF3 Ensembl:ENSG00000161405 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4795396 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_6354 50426 RMVar_ID_50426 Human_SNP_ID_623955017 A-to-I Human chr17 - 39859585 39859585 39859585 TGGGACTTCAAGACCAGCCTGGGCAACATGGTAAAACCCTGACTCTACAAAAACTACAAAAATTA TGGGACTTCAAGACCAGCCTGGGCAACATGGTGAAACCCTGACTCTACAAAAACTACAAAAATTA T C IKZF3 Ensembl:ENSG00000161405 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1405368284 Functional Loss SNV dbSNP153 33..33 33 - - - 50427 RMVar_ID_50427 Human_SNP_ID_623966208 A-to-I Human chr17 - 39907500 39907500 39907500 AGGGTTTCACTATATGTTGGCAGGCTGCTCTCAAACTCCTGAACTCAGGTGATCCACCCACTGCA AGGGTTTCACTATATGTTGGCAGGCTGCTCTCGAACTCCTGAACTCAGGTGATCCACCCACTGCA T C GSDMB Ensembl:ENSG00000073605 Protein coding exon GSE47997;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 K562 cells&HepG2 cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 23474544,29129909,31158229 RNA-Seq:(High) rs1329596753 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_62320,RMVar_hsa_circ_62679,RMVar_hsa_circ_58590 50428 RMVar_ID_50428 Human_SNP_ID_623968917 A-to-I Human chr17 - 39917778 39917778 39917778 CATGTGAAGAGAGTCCACGAAACGGGCTTTATATGAGCAACAAGGCTGGGTGCAGGCAAGCTGAG CATGTGAAGAGAGTCCACGAAACGGGCTTTATTTGAGCAACAAGGCTGGGTGCAGGCAAGCTGAG T A GSDMB Ensembl:ENSG00000073605 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs9303280 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_6355,GWAS_ID_6356,GWAS_ID_6357,GWAS_ID_6358,GWAS_ID_6359,GWAS_ID_6360,GWAS_ID_6361,GWAS_ID_6362,GWAS_ID_6363,GWAS_ID_6364,GWAS_ID_6365,GWAS_ID_6366,GWAS_ID_6367,GWAS_ID_6368,GWAS_ID_6369,GWAS_ID_6370,GWAS_ID_6371,GWAS_ID_6372,GWAS_ID_6373,GWAS_ID_6374,GWAS_ID_6375,GWAS_ID_6376,GWAS_ID_6377,GWAS_ID_6378,GWAS_ID_6379,GWAS_ID_6380,GWAS_ID_6381,GWAS_ID_6382,GWAS_ID_6383,GWAS_ID_6384,GWAS_ID_6385,GWAS_ID_6386,GWAS_ID_6387,GWAS_ID_6388,GWAS_ID_6389,GWAS_ID_6390,GWAS_ID_6391,GWAS_ID_6392,GWAS_ID_6393,GWAS_ID_6394,GWAS_ID_6395,GWAS_ID_6396,GWAS_ID_6397,GWAS_ID_6398,GWAS_ID_6399,GWAS_ID_6400,GWAS_ID_6401,GWAS_ID_6402,GWAS_ID_6403,GWAS_ID_6404,GWAS_ID_6405,GWAS_ID_6406,GWAS_ID_6407,GWAS_ID_6408,GWAS_ID_6409,GWAS_ID_6410,GWAS_ID_6411,GWAS_ID_6412,GWAS_ID_6413,GWAS_ID_6414,GWAS_ID_6415,GWAS_ID_6416,GWAS_ID_6417,GWAS_ID_6418,GWAS_ID_6419,GWAS_ID_6420,GWAS_ID_6421,GWAS_ID_6422,GWAS_ID_6423,GWAS_ID_6424,GWAS_ID_6425,GWAS_ID_6426,GWAS_ID_6427,GWAS_ID_6428 50429 RMVar_ID_50429 Human_SNP_ID_623968918 A-to-I Human chr17 - 39917778 39917778 39917778 CATGTGAAGAGAGTCCACGAAACGGGCTTTATATGAGCAACAAGGCTGGGTGCAGGCAAGCTGAG CATGTGAAGAGAGTCCACGAAACGGGCTTTATGTGAGCAACAAGGCTGGGTGCAGGCAAGCTGAG T C GSDMB Ensembl:ENSG00000073605 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs9303280 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_6355,GWAS_ID_6356,GWAS_ID_6357,GWAS_ID_6358,GWAS_ID_6359,GWAS_ID_6360,GWAS_ID_6361,GWAS_ID_6362,GWAS_ID_6363,GWAS_ID_6364,GWAS_ID_6365,GWAS_ID_6366,GWAS_ID_6367,GWAS_ID_6368,GWAS_ID_6369,GWAS_ID_6370,GWAS_ID_6371,GWAS_ID_6372,GWAS_ID_6373,GWAS_ID_6374,GWAS_ID_6375,GWAS_ID_6376,GWAS_ID_6377,GWAS_ID_6378,GWAS_ID_6379,GWAS_ID_6380,GWAS_ID_6381,GWAS_ID_6382,GWAS_ID_6383,GWAS_ID_6384,GWAS_ID_6385,GWAS_ID_6386,GWAS_ID_6387,GWAS_ID_6388,GWAS_ID_6389,GWAS_ID_6390,GWAS_ID_6391,GWAS_ID_6392,GWAS_ID_6393,GWAS_ID_6394,GWAS_ID_6395,GWAS_ID_6396,GWAS_ID_6397,GWAS_ID_6398,GWAS_ID_6399,GWAS_ID_6400,GWAS_ID_6401,GWAS_ID_6402,GWAS_ID_6403,GWAS_ID_6404,GWAS_ID_6405,GWAS_ID_6406,GWAS_ID_6407,GWAS_ID_6408,GWAS_ID_6409,GWAS_ID_6410,GWAS_ID_6411,GWAS_ID_6412,GWAS_ID_6413,GWAS_ID_6414,GWAS_ID_6415,GWAS_ID_6416,GWAS_ID_6417,GWAS_ID_6418,GWAS_ID_6419,GWAS_ID_6420,GWAS_ID_6421,GWAS_ID_6422,GWAS_ID_6423,GWAS_ID_6424,GWAS_ID_6425,GWAS_ID_6426,GWAS_ID_6427,GWAS_ID_6428 50430 RMVar_ID_50430 Human_SNP_ID_623969457 A-to-I Human chr17 - 39919711 39919711 39919711 TGGCTAATTTTTTTTTTTTTTTTTTTTTTGGTAGAGACGGGGTTTCGCCATGTTGGCCAGGCTGG TGGCTAATTTTTTTTTTTTTTTTTTTTTTGGTGGAGACGGGGTTTCGCCATGTTGGCCAGGCTGG T C GSDMB Ensembl:ENSG00000073605 Protein coding exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1045064786 Functional Loss SNV dbSNP153 33..33 33 - - - 50431 RMVar_ID_50431 Human_SNP_ID_623986364 A-to-I Human chr17 + 39984371 39984371 39984371 AGGAGCCGAGATTCGTGCTGCGGGCCCTGCGGATGCTGCCTTCCACATCACGCCGCCTCAACCAC AGGAGCCGAGATTCGTGCTGCGGGCCCTGCGGTTGCTGCCTTCCACATCACGCCGCCTCAACCAC A T PSMD3 Ensembl:ENSG00000108344 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1056285438 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_903635,Human_RBP_ID_3522370,Human_RBP_ID_5144156,Human_RBP_ID_6592205,Human_RBP_ID_8817388,Human_RBP_ID_9289014,Human_RBP_ID_17891592,Human_RBP_ID_22444512,Human_RBP_ID_22499353 Human_Splice_Rec_1813126 Human_miRNA_ID_1938255,Human_miRNA_ID_1949355,Human_miRNA_ID_2932778 RMVar_hsa_circ_113219,RMVar_hsa_circ_183986,RMVar_hsa_circ_323197,RMVar_hsa_circ_353966 50432 RMVar_ID_50432 Human_SNP_ID_623988240 A-to-I Human chr17 + 39991914 39991914 39991914 GGGCGTGATGGCATGCACCTGTAGTCCCAGCTACTTGGGAGGCTGAGGTGCAAGGATCACTTGGG GGGCGTGATGGCATGCACCTGTAGTCCCAGCTGCTTGGGAGGCTGAGGTGCAAGGATCACTTGGG A G PSMD3 Ensembl:ENSG00000108344 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs751455171 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92561,RMVar_hsa_circ_89938,RMVar_hsa_circ_183989,RMVar_hsa_circ_3124,RMVar_hsa_circ_183988,RMVar_hsa_circ_183994,RMVar_hsa_circ_90924 50433 RMVar_ID_50433 Human_SNP_ID_623988261 A-to-I Human chr17 + 39992007 39992007 39992007 TGATCGTGCCACTGCACTGCAGCCTGGGCGACAGAGCAAGACTCTGTCTCAAAAAAAAACAAACA TGATCGTGCCACTGCACTGCAGCCTGGGCGACGGAGCAAGACTCTGTCTCAAAAAAAAACAAACA A G PSMD3 Ensembl:ENSG00000108344 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1246971018 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92561,RMVar_hsa_circ_89938,RMVar_hsa_circ_183989,RMVar_hsa_circ_3124,RMVar_hsa_circ_183988,RMVar_hsa_circ_183994,RMVar_hsa_circ_90924 50434 RMVar_ID_50434 Human_SNP_ID_623997758 A-to-I Human chr17 - 40024452 40024452 40024452 TAGGCTCACTGCAATCTCCGCCTCCTGGGTTCAAGAGATTCTCCTGCCTCAGCCTCCCGAGTAGC TAGGCTCACTGCAATCTCCGCCTCCTGGGTTCGAGAGATTCTCCTGCCTCAGCCTCCCGAGTAGC T C MED24 Ensembl:ENSG00000008838 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1361241657 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 50435 RMVar_ID_50435 Human_SNP_ID_623997759 A-to-I Human chr17 - 40024452 40024452 40024452 TAGGCTCACTGCAATCTCCGCCTCCTGGGTTCAAGAGATTCTCCTGCCTCAGCCTCCCGAGTAGC TAGGCTCACTGCAATCTCCGCCTCCTGGGTTCCAGAGATTCTCCTGCCTCAGCCTCCCGAGTAGC T G MED24 Ensembl:ENSG00000008838 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1361241657 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 50436 RMVar_ID_50436 Human_SNP_ID_624004765 A-to-I Human chr17 - 40050364 40050364 40050364 CTGCTTACTGTGACCTCCACCTCCTGGGCTCAAGTGATTCTTCTGCCTGTCTCCCGAGTAGCTGG CTGCTTACTGTGACCTCCACCTCCTGGGCTCAGGTGATTCTTCTGCCTGTCTCCCGAGTAGCTGG T C MED24 Ensembl:ENSG00000008838 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560247319 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12996531 RMVar_hsa_circ_184002,RMVar_hsa_circ_113893,RMVar_hsa_circ_347766 50437 RMVar_ID_50437 Human_SNP_ID_624005452 A-to-I Human chr17 - 40053009 40053009 40053009 GATCACCTGAGCCCTGGGAGGTCGAGACTGCAATGAGCCATGATCCTGCCACTGCCCTCCAGCCA GATCACCTGAGCCCTGGGAGGTCGAGACTGCAGTGAGCCATGATCCTGCCACTGCCCTCCAGCCA T C MED24 Ensembl:ENSG00000008838 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs957477437 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25281151 RMVar_hsa_circ_184002,RMVar_hsa_circ_113893,RMVar_hsa_circ_347766 50438 RMVar_ID_50438 Human_SNP_ID_624023210 A-to-I Human chr17 - 40118899 40118899 40118899 AAATTTAGCCGAGCCTGGTGGCAGGGGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA AAATTTAGCCGAGCCTGGTGGCAGGGGCCTGTGGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGA T C lnc-NR1D1-1,lnc-NR1D1-1:2,lnc-NR1D1-1:3,lnc-NR1D1-1:4,lnc-NR1D1-1:5 RNACentral:URS0000D5A831,RNACentral:URS0000D5A2C4,RNACentral:URS0000D580D8,RNACentral:URS0000D5CADC,RNACentral:URS0000D5DAED lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,intron,exon,exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048125283 Functional Loss SNV dbSNP153 33..33 33 - - - 50439 RMVar_ID_50439 Human_SNP_ID_624023530 A-to-I Human chr17 - 40119937 40119937 40119937 GTTGGATGTCTAATAGGTATTTCTTTTTTTTGAGGTGGAGTCTTGCTCTGTTGCCCAGGCTGGAG GTTGGATGTCTAATAGGTATTTCTTTTTTTTGTGGTGGAGTCTTGCTCTGTTGCCCAGGCTGGAG T A 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 RNACentral:URS00008B80DC,RNACentral:URS0000D5A831,RNACentral:URS0000D5A2C4,RNACentral:URS0000D580D8,RNACentral:URS0000D5CADC,RNACentral:URS0000D5DAED,RNACentral:URS00008BE8F3 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,intron,exon,exon,exon,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs962575634 Functional Loss SNV dbSNP153 33..33 33 - - - 50440 RMVar_ID_50440 Human_SNP_ID_624033102 A-to-I Human chr17 + 40154399 40154399 40154399 GGGATTACAGGTGTGCGCTGCCATGCCCGGCTAATTTTTGTATTTTTAGTAGAGACGAGGTTTTG GGGATTACAGGTGTGCGCTGCCATGCCCGGCTGATTTTTGTATTTTTAGTAGAGACGAGGTTTTG A G CASC3 Ensembl:ENSG00000108349 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1003551235 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 50441 RMVar_ID_50441 Human_SNP_ID_624037162 A-to-I Human chr17 - 40169594 40169594 40169594 TTGTATTAACTGGAACCCCTGCTTACAACCTGAAATAACAAAGTTGGAATTTGTTATCAGGTCAT TTGTATTAACTGGAACCCCTGCTTACAACCTGGAATAACAAAGTTGGAATTTGTTATCAGGTCAT T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs761079576 Functional Loss SNV dbSNP153 33..33 33 - - - 50442 RMVar_ID_50442 Human_SNP_ID_624041186 A-to-I Human chr17 + 40184856 40184856 40184856 GGCTGGAGAGCAGTGGTGCGATCTCGGCTCACAGCAACCTCCACCTCTTGGGTTGAAGTGATTCT GGCTGGAGAGCAGTGGTGCGATCTCGGCTCACGGCAACCTCCACCTCTTGGGTTGAAGTGATTCT A G RAPGEFL1 Ensembl:ENSG00000108352 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs899692448 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57444,RMVar_hsa_circ_378488,RMVar_hsa_circ_93653,RMVar_hsa_circ_121623,RMVar_hsa_circ_184032,RMVar_hsa_circ_184033 50443 RMVar_ID_50443 Human_SNP_ID_624041188 A-to-I Human chr17 + 40184866 40184866 40184866 CAGTGGTGCGATCTCGGCTCACAGCAACCTCCACCTCTTGGGTTGAAGTGATTCTCATGCCTCAG CAGTGGTGCGATCTCGGCTCACAGCAACCTCCGCCTCTTGGGTTGAAGTGATTCTCATGCCTCAG A G RAPGEFL1 Ensembl:ENSG00000108352 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1440771869 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_57444,RMVar_hsa_circ_378488,RMVar_hsa_circ_93653,RMVar_hsa_circ_121623,RMVar_hsa_circ_184032,RMVar_hsa_circ_184033 50444 RMVar_ID_50444 Human_SNP_ID_624053976 A-to-I Human chr17 + 40229650 40229650 40229650 ACCATGTTGGCCAGGCTGGCCTCAAAACTCCTAACCTCAAGTGATCTTCCTGCCTCGGCCTCCTA ACCATGTTGGCCAGGCTGGCCTCAAAACTCCTGACCTCAAGTGATCTTCCTGCCTCGGCCTCCTA A G WIPF2 Ensembl:ENSG00000171475 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs956752869 Functional Loss SNV dbSNP153 33..33 33 - - - 50445 RMVar_ID_50445 Human_SNP_ID_624055121 A-to-I Human chr17 + 40234220 40234220 40234220 AAAACCCTGTCTCTACTAAAAATACAAAAATTAGCTGGGTGTGGTGGCAAGTGCCTGTAGTCCCA AAAACCCTGTCTCTACTAAAAATACAAAAATTCGCTGGGTGTGGTGGCAAGTGCCTGTAGTCCCA A C WIPF2 Ensembl:ENSG00000171475 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934762877 Functional Loss SNV dbSNP153 33..33 33 - - - 50446 RMVar_ID_50446 Human_SNP_ID_624055428 A-to-I Human chr17 + 40235169 40235169 40235169 CGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCTTGAGCCACCACGCCCAGCCCATTGTG CGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTGCAGGCTTGAGCCACCACGCCCAGCCCATTGTG A G WIPF2 Ensembl:ENSG00000171475 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs374932550 Functional Loss SNV dbSNP153 33..33 33 - - - 50447 RMVar_ID_50447 Human_SNP_ID_624055626 A-to-I Human chr17 + 40235854 40235854 40235854 TCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCGCCTGGCCTCTGGAGAGTGGG TCTTGGCCTCCCAAAGTGCTGGGATTACAGGCTTGAGCCACCGCGCCTGGCCTCTGGAGAGTGGG A T WIPF2 Ensembl:ENSG00000171475 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1233743178 Functional Loss SNV dbSNP153 33..33 33 - - - 50448 RMVar_ID_50448 Human_SNP_ID_624061557 A-to-I Human chr17 + 40257557 40257557 40257557 ACCTGAGGCCAGGCGCGATGGCTCACGCCTGTAATCCCAACACTTTGGGAGGCTGAGGTGGGTGG ACCTGAGGCCAGGCGCGATGGCTCACGCCTGTTATCCCAACACTTTGGGAGGCTGAGGTGGGTGG A T WIPF2 Ensembl:ENSG00000171475 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1238074095 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_184037,RMVar_hsa_circ_327377,RMVar_hsa_circ_377483,RMVar_hsa_circ_296932 50449 RMVar_ID_50449 Human_SNP_ID_624061560 A-to-I Human chr17 + 40257563 40257563 40257563 GGCCAGGCGCGATGGCTCACGCCTGTAATCCCAACACTTTGGGAGGCTGAGGTGGGTGGATTGCT GGCCAGGCGCGATGGCTCACGCCTGTAATCCCGACACTTTGGGAGGCTGAGGTGGGTGGATTGCT A G WIPF2 Ensembl:ENSG00000171475 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1054528077 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_184037,RMVar_hsa_circ_327377,RMVar_hsa_circ_377483,RMVar_hsa_circ_296932 50450 RMVar_ID_50450 Human_SNP_ID_624064472 A-to-I Human chr17 + 40267685 40267685 40267685 TCTCAGCCTCCTGACTAGCTGGAATTACAGGCATGTGCCACCATATCTGGCTAATTTTTGTATTT TCTCAGCCTCCTGACTAGCTGGAATTACAGGCGTGTGCCACCATATCTGGCTAATTTTTGTATTT A G WIPF2 Ensembl:ENSG00000171475 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs762249258 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_327377 50451 RMVar_ID_50451 Human_SNP_ID_624066182 A-to-I Human chr17 + 40274426 40274426 40274426 TTCTTGGAATTATTATTTTTTAATTATTTTTTATAGAGACTGGGTCTCTGTTGCCCAGGCCGCTG TTCTTGGAATTATTATTTTTTAATTATTTTTTGTAGAGACTGGGTCTCTGTTGCCCAGGCCGCTG A G WIPF2 Ensembl:ENSG00000171475 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1316320944 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6592880 RMVar_hsa_circ_327377,RMVar_hsa_circ_367753 50452 RMVar_ID_50452 Human_SNP_ID_624067028 A-to-I Human chr17 + 40277424 40277424 40277424 CAAAATTAGGCTGGGCGCGGTGGCTTATGCCTATAATCCCAGCATTTTGGGAGGCTGAGGTGGGC CAAAATTAGGCTGGGCGCGGTGGCTTATGCCTGTAATCCCAGCATTTTGGGAGGCTGAGGTGGGC A G WIPF2 Ensembl:ENSG00000171475 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1042908430 Functional Loss SNV dbSNP153 33..33 33 - - - 50453 RMVar_ID_50453 Human_SNP_ID_624067186 A-to-I Human chr17 + 40277852 40277852 40277852 AGGTTCAAGTGATTCTCCTGCTTAAGCCTCCCAAGTATCTAGGATTATAGGCGTGTGCCACCATG AGGTTCAAGTGATTCTCCTGCTTAAGCCTCCCGAGTATCTAGGATTATAGGCGTGTGCCACCATG A G WIPF2 Ensembl:ENSG00000171475 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1431971811 Functional Loss SNV dbSNP153 33..33 33 - - - 50454 RMVar_ID_50454 Human_SNP_ID_624068460 A-to-I Human chr17 + 40283127 40283127 40283127 AAAATCACTTGAACCCAGGAGGCGGAGGTTGCACTGAGCTGAGATCATGCCACTGCACTAAAAAA AAAATCACTTGAACCCAGGAGGCGGAGGTTGCGCTGAGCTGAGATCATGCCACTGCACTAAAAAA A G WIPF2 Ensembl:ENSG00000171475 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1387124470 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25281748 50455 RMVar_ID_50455 Human_SNP_ID_624068583 A-to-I Human chr17 + 40283430 40283430 40283430 CTATGCCTGGCTAATTTTGAAAATTTTTTTGTAAAGACAGGGTCTCCCTATGTTGCCCAGACTGG CTATGCCTGGCTAATTTTGAAAATTTTTTTGTGAAGACAGGGTCTCCCTATGTTGCCCAGACTGG A G WIPF2 Ensembl:ENSG00000171475 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1433176184 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_488863 50456 RMVar_ID_50456 Human_SNP_ID_624068589 A-to-I Human chr17 + 40283456 40283456 40283456 TTTTGTAAAGACAGGGTCTCCCTATGTTGCCCAGACTGGTCTCAAATTCCTGGGCTTAAGTGATT TTTTGTAAAGACAGGGTCTCCCTATGTTGCCCTGACTGGTCTCAAATTCCTGGGCTTAAGTGATT A T WIPF2 Ensembl:ENSG00000171475 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1275784296 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_488863 50457 RMVar_ID_50457 Human_SNP_ID_624068593 A-to-I Human chr17 + 40283494 40283494 40283494 GTCTCAAATTCCTGGGCTTAAGTGATTGTCCCACCTCAGCTTCTCAAAGTGCTGGGATTACAGGC GTCTCAAATTCCTGGGCTTAAGTGATTGTCCCGCCTCAGCTTCTCAAAGTGCTGGGATTACAGGC A G WIPF2 Ensembl:ENSG00000171475 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1333511725 Functional Loss SNV dbSNP153 33..33 33 - - - 50458 RMVar_ID_50458 Human_SNP_ID_624068596 A-to-I Human chr17 + 40283499 40283499 40283499 AAATTCCTGGGCTTAAGTGATTGTCCCACCTCAGCTTCTCAAAGTGCTGGGATTACAGGCATGAG AAATTCCTGGGCTTAAGTGATTGTCCCACCTCGGCTTCTCAAAGTGCTGGGATTACAGGCATGAG A G WIPF2 Ensembl:ENSG00000171475 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1043684209 Functional Loss SNV dbSNP153 33..33 33 - - - 50459 RMVar_ID_50459 Human_SNP_ID_624081295 A-to-I Human chr17 + 40336662 40336662 40336662 CGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCGCCCGGCTTGTTGTT CGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTGCAGGCATGAGCCACCGCGCCCGGCTTGTTGTT A G RARA Ensembl:ENSG00000131759 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs960135789 Functional Loss SNV dbSNP153 33..33 33 - - - 50460 RMVar_ID_50460 Human_SNP_ID_624097549 A-to-I Human chr17 - 40394465 40394465 40394465 AGTTGAGTGTGGTGGTGCGTGCCTGTAGTCCCAGCTACTCGAGAGGCTGAGGCACGAGTGTCGCT AGTTGAGTGTGGTGGTGCGTGCCTGTAGTCCCCGCTACTCGAGAGGCTGAGGCACGAGTGTCGCT T G TOP2A Ensembl:ENSG00000131747 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs906308685 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100364,RMVar_hsa_circ_114820,RMVar_hsa_circ_125443,RMVar_hsa_circ_115471,RMVar_hsa_circ_108745,RMVar_hsa_circ_111120,RMVar_hsa_circ_101665,RMVar_hsa_circ_184051,RMVar_hsa_circ_77193,RMVar_hsa_circ_96531,RMVar_hsa_circ_86476,RMVar_hsa_circ_184055,RMVar_hsa_circ_184057,RMVar_hsa_circ_184058,RMVar_hsa_circ_184056,RMVar_hsa_circ_184053,RMVar_hsa_circ_184054,RMVar_hsa_circ_184052,RMVar_hsa_circ_121719,RMVar_hsa_circ_184049,RMVar_hsa_circ_184050,RMVar_hsa_circ_184061,RMVar_hsa_circ_106603,RMVar_hsa_circ_347242,RMVar_hsa_circ_125479,RMVar_hsa_circ_38172,RMVar_hsa_circ_86059,RMVar_hsa_circ_184063,RMVar_hsa_circ_184062,RMVar_hsa_circ_48031,RMVar_hsa_circ_184065 50461 RMVar_ID_50461 Human_SNP_ID_624097881 A-to-I Human chr17 - 40395752 40395752 40395752 TCCCAAGTAGTTGGGGGCACATCACCACACCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGT TCCCAAGTAGTTGGGGGCACATCACCACACCCGGCTAATTTTTGTATTTTTAGTAGAGATGGGGT T C TOP2A Ensembl:ENSG00000131747 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs977798511 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100364,RMVar_hsa_circ_114820,RMVar_hsa_circ_125443,RMVar_hsa_circ_115471,RMVar_hsa_circ_108745,RMVar_hsa_circ_111120,RMVar_hsa_circ_101665,RMVar_hsa_circ_1070,RMVar_hsa_circ_184051,RMVar_hsa_circ_77193,RMVar_hsa_circ_96531,RMVar_hsa_circ_86476,RMVar_hsa_circ_184055,RMVar_hsa_circ_184057,RMVar_hsa_circ_184058,RMVar_hsa_circ_184056,RMVar_hsa_circ_184053,RMVar_hsa_circ_184054,RMVar_hsa_circ_184052,RMVar_hsa_circ_121719,RMVar_hsa_circ_184049,RMVar_hsa_circ_184050,RMVar_hsa_circ_184061,RMVar_hsa_circ_106603,RMVar_hsa_circ_125479,RMVar_hsa_circ_38172,RMVar_hsa_circ_86059,RMVar_hsa_circ_184063,RMVar_hsa_circ_184062,RMVar_hsa_circ_48031,RMVar_hsa_circ_184065,RMVar_hsa_circ_273777,RMVar_hsa_circ_296988,RMVar_hsa_circ_184066,RMVar_hsa_circ_184067 50462 RMVar_ID_50462 Human_SNP_ID_624099675 A-to-I Human chr17 - 40402956 40402956 40402956 TTGCAGCCCATTGGTCAGTTTGGTACCAGGCTACATGGTGGCAAGGATTCTGCTAGTCCACGATA TTGCAGCCCATTGGTCAGTTTGGTACCAGGCTGCATGGTGGCAAGGATTCTGCTAGTCCACGATA T C TOP2A Ensembl:ENSG00000131747 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs766736084 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_47919,Human_RBP_ID_278842,Human_RBP_ID_488928,Human_RBP_ID_1533471,Human_RBP_ID_1857695,Human_RBP_ID_3522783,Human_RBP_ID_4425543,Human_RBP_ID_5186503,Human_RBP_ID_8817626,Human_RBP_ID_9257830,Human_RBP_ID_9289037,Human_RBP_ID_17491139,Human_RBP_ID_22444526,Human_RBP_ID_26960491,Human_RBP_ID_27665000 Human_Splice_Rec_1814558,Human_Splice_Rec_1814559 Human_miRNA_ID_2490739,Human_miRNA_ID_2752824 RMVar_hsa_circ_100364,RMVar_hsa_circ_114820,RMVar_hsa_circ_125443,RMVar_hsa_circ_115471,RMVar_hsa_circ_108745,RMVar_hsa_circ_184051,RMVar_hsa_circ_77193,RMVar_hsa_circ_96531,RMVar_hsa_circ_86476,RMVar_hsa_circ_184055,RMVar_hsa_circ_184056,RMVar_hsa_circ_184053,RMVar_hsa_circ_184054,RMVar_hsa_circ_184052,RMVar_hsa_circ_184049,RMVar_hsa_circ_184050,RMVar_hsa_circ_184061,RMVar_hsa_circ_106603,RMVar_hsa_circ_38172,RMVar_hsa_circ_86059,RMVar_hsa_circ_184062,RMVar_hsa_circ_48031,RMVar_hsa_circ_10065,RMVar_hsa_circ_1728,RMVar_hsa_circ_28374,RMVar_hsa_circ_61778,RMVar_hsa_circ_91428,RMVar_hsa_circ_317857,RMVar_hsa_circ_356190,RMVar_hsa_circ_184069,RMVar_hsa_circ_347088,RMVar_hsa_circ_47507,RMVar_hsa_circ_47990,RMVar_hsa_circ_82089,RMVar_hsa_circ_184070,RMVar_hsa_circ_13135,RMVar_hsa_circ_123445,RMVar_hsa_circ_9984,RMVar_hsa_circ_42735,RMVar_hsa_circ_184071,RMVar_hsa_circ_23101 50463 RMVar_ID_50463 Human_SNP_ID_624101768 A-to-I Human chr17 - 40411351 40411351 40411351 AAGGGTGGTGTTGCAGTAAAAGCACATCAGGTATGTGCTTTTGGCAGTTTTCTTTTTCTAAAGTC AAGGGTGGTGTTGCAGTAAAAGCACATCAGGTGTGTGCTTTTGGCAGTTTTCTTTTTCTAAAGTC T C TOP2A Ensembl:ENSG00000131747 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs1490094899 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1857738,Human_RBP_ID_26960521 RMVar_hsa_circ_100364,RMVar_hsa_circ_125443,RMVar_hsa_circ_115471,RMVar_hsa_circ_108745,RMVar_hsa_circ_9053,RMVar_hsa_circ_184051,RMVar_hsa_circ_184052,RMVar_hsa_circ_184049,RMVar_hsa_circ_184050,RMVar_hsa_circ_86059,RMVar_hsa_circ_184062,RMVar_hsa_circ_28374,RMVar_hsa_circ_317857,RMVar_hsa_circ_356190,RMVar_hsa_circ_82089,RMVar_hsa_circ_184070,RMVar_hsa_circ_13135,RMVar_hsa_circ_9984,RMVar_hsa_circ_42735,RMVar_hsa_circ_294522,RMVar_hsa_circ_184074,RMVar_hsa_circ_54518,RMVar_hsa_circ_75141,RMVar_hsa_circ_17240,RMVar_hsa_circ_268695,RMVar_hsa_circ_359702,RMVar_hsa_circ_346992 50464 RMVar_ID_50464 Human_SNP_ID_624102332 A-to-I Human chr17 - 40413849 40413849 40413849 GAATCACAGGCATGCGCTACCATGCCTGGCTAATTTTTTTTATTTTTAGTAGAGACGGTTTCAAC GAATCACAGGCATGCGCTACCATGCCTGGCTAGTTTTTTTTATTTTTAGTAGAGACGGTTTCAAC T C TOP2A Ensembl:ENSG00000131747 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs895158141 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125443,RMVar_hsa_circ_108745,RMVar_hsa_circ_9053,RMVar_hsa_circ_184049,RMVar_hsa_circ_184050,RMVar_hsa_circ_28374,RMVar_hsa_circ_356190,RMVar_hsa_circ_13135,RMVar_hsa_circ_42735,RMVar_hsa_circ_17240,RMVar_hsa_circ_359702,RMVar_hsa_circ_64492,RMVar_hsa_circ_73367,RMVar_hsa_circ_362828 50465 RMVar_ID_50465 Human_SNP_ID_624117534 A-to-I Human chr17 - 40475276 40475276 40475276 ACCTAGGAGTTCGAGACCAGCCTGGGCAACATAGGGAGACCCTGTCTCTACAAAAAAAATACAAA ACCTAGGAGTTCGAGACCAGCCTGGGCAACATGGGGAGACCCTGTCTCTACAAAAAAAATACAAA T C AC018629.1 Ensembl:ENSG00000279806 Other exon GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1404133305 Functional Loss SNV dbSNP153 33..33 33 - - - 50466 RMVar_ID_50466 Human_SNP_ID_624117557 A-to-I Human chr17 - 40475356 40475356 40475356 GAGCTGGACTGTGGTCGGGTGTGGTGGCTCGCACCTGTAATCCCAGCACTTTGGGAGGCCAAAGC GAGCTGGACTGTGGTCGGGTGTGGTGGCTCGCGCCTGTAATCCCAGCACTTTGGGAGGCCAAAGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1032229405 Functional Loss SNV dbSNP153 33..33 33 - - - 50467 RMVar_ID_50467 Human_SNP_ID_624216412 A-to-I Human chr17 - 40881880 40881879 40881880 CAACAGACTGAGACCTTGTCTCAAAAAAAAAAAGGAAGAAAGAAAGAAAAGAAAAAGAAAGTAAA CAACAGACTGAGACCTTGTCTCAAAAAAAAAA_GGAAGAAAGAAAGAAAAGAAAAAGAAAGTAAA CT C KRT20 Ensembl:ENSG00000171431 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs112248312 Functional Loss DEL dbSNP153 33..33 33 - - - 50468 RMVar_ID_50468 Human_SNP_ID_624217506 A-to-I Human chr17 + 40886060 40886060 40886060 CTCTTTTGTATGAGGCCAGCTTAACACCCACCATGAGACAGACTCTGCCCCATCCATCCTGAAGC CTCTTTTGTATGAGGCCAGCTTAACACCCACCGTGAGACAGACTCTGCCCCATCCATCCTGAAGC A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs934659204 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27452051 50469 RMVar_ID_50469 Human_SNP_ID_624230474 A-to-I Human chr17 - 40939701 40939701 40939701 TGTGGTCCCGGCTACTCGGGAGGCTGAGGCAGAAGAATCGCTTGAACCCGGGAGGTGGAGGTTGC TGTGGTCCCGGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGGGAGGTGGAGGTTGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1332978941 Functional Loss SNV dbSNP153 33..33 33 - - - 50470 RMVar_ID_50470 Human_SNP_ID_624454497 A-to-I Human chr17 - 41751455 41751455 41751455 CTCATGCGTAATTGGGATTACAGACTACAGGTACACACCACAATGCCTGGCTAGTTTTTTTTTTT CTCATGCGTAATTGGGATTACAGACTACAGGTGCACACCACAATGCCTGGCTAGTTTTTTTTTTT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1229664394 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 50471 RMVar_ID_50471 Human_SNP_ID_624455525 A-to-I Human chr17 - 41755037 41755037 41755037 ACTGCCCTAAGCCCCCAGGGCCTCCAGGGCCCAGGTTCGAGACCCAAACCCCCAAAATCCAAAAC ACTGCCCTAAGCCCCCAGGGCCTCCAGGGCCCGGGTTCGAGACCCAAACCCCCAAAATCCAAAAC T C JUP Ensembl:ENSG00000173801 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs534941603 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_49130,Human_RBP_ID_489144,Human_RBP_ID_17080265,Human_RBP_ID_17262897,Human_RBP_ID_17378354,Human_RBP_ID_18697465,Human_RBP_ID_26450529,Human_RBP_ID_27452103 Human_miRNA_ID_1414882,Human_miRNA_ID_2724246,Human_miRNA_ID_2724247,Human_miRNA_ID_2724248 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 50472 RMVar_ID_50472 Human_SNP_ID_624461475 A-to-I Human chr17 - 41774466 41774466 41774466 AGCCAGGCGTGGTGGTGCACACCTGTAGTCCCAGCTACTTCAGAGGTTGAGGCAGGAGAATCACT AGCCAGGCGTGGTGGTGCACACCTGTAGTCCCTGCTACTTCAGAGGTTGAGGCAGGAGAATCACT T A JUP Ensembl:ENSG00000173801 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1298563133 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121896,RMVar_hsa_circ_86967,RMVar_hsa_circ_184187,RMVar_hsa_circ_184188 50473 RMVar_ID_50473 Human_SNP_ID_624461580 A-to-I Human chr17 - 41774909 41774909 41774909 TTTAGTAGAGACAGGATTTCACCATGTTGACCAGGATGGTCTTGAACTCCTGACCTCGTGATCTG TTTAGTAGAGACAGGATTTCACCATGTTGACCCGGATGGTCTTGAACTCCTGACCTCGTGATCTG T G JUP Ensembl:ENSG00000173801 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1236174541 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121896,RMVar_hsa_circ_86967,RMVar_hsa_circ_184187,RMVar_hsa_circ_184188 50474 RMVar_ID_50474 Human_SNP_ID_624462451 A-to-I Human chr17 - 41778484 41778484 41778484 CAGCTCACTGCAACCTCCTCTTCCTGGGCTCAAGCGATCCTCCTACCTCAGCCTCCCAAGTAGCT CAGCTCACTGCAACCTCCTCTTCCTGGGCTCATGCGATCCTCCTACCTCAGCCTCCCAAGTAGCT T A JUP Ensembl:ENSG00000173801 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1326207156 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1915006,Human_miRNA_ID_1917455,Human_miRNA_ID_1919907,Human_miRNA_ID_1922366,Human_miRNA_ID_1924820,Human_miRNA_ID_1927271,Human_miRNA_ID_1929720,Human_miRNA_ID_3125856 RMVar_hsa_circ_121896,RMVar_hsa_circ_86967,RMVar_hsa_circ_184187,RMVar_hsa_circ_184188 50475 RMVar_ID_50475 Human_SNP_ID_624462809 A-to-I Human chr17 - 41779509 41779509 41779509 CCTGGCTAACATGGTGAAACCCCGTCTCTACTAAAAAATACAAAGAATTAGCTGGGCGTTGTGGC CCTGGCTAACATGGTGAAACCCCGTCTCTACTGAAAAATACAAAGAATTAGCTGGGCGTTGTGGC T C JUP Ensembl:ENSG00000173801 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs902519580 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121896,RMVar_hsa_circ_86967,RMVar_hsa_circ_184187,RMVar_hsa_circ_184188 50476 RMVar_ID_50476 Human_SNP_ID_624462936 A-to-I Human chr17 - 41779948 41779948 41779948 ATATCTGGCTGGGGCAGTGGCTTACACCTGTAATCCCAACCGCTCTGAAGGTTGAGGCAGGAGGA ATATCTGGCTGGGGCAGTGGCTTACACCTGTAGTCCCAACCGCTCTGAAGGTTGAGGCAGGAGGA T C JUP Ensembl:ENSG00000173801 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1198105894 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121896,RMVar_hsa_circ_86967,RMVar_hsa_circ_184187,RMVar_hsa_circ_184188 50477 RMVar_ID_50477 Human_SNP_ID_624464047 A-to-I Human chr17 - 41783803 41783803 41783803 GTGATTCTCCTGCCTCAGCCTCCTGAGTAGCCAGGATTACAGGCGTGTGCCACCACCCCCGGCTG GTGATTCTCCTGCCTCAGCCTCCTGAGTAGCCGGGATTACAGGCGTGTGCCACCACCCCCGGCTG T C JUP Ensembl:ENSG00000173801 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1489762130 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121896,RMVar_hsa_circ_86967,RMVar_hsa_circ_184187,RMVar_hsa_circ_184188 50478 RMVar_ID_50478 Human_SNP_ID_624468942 A-to-I Human chr17 - 41802154 41802154 41802154 CCACAGGATGGTGGTGGCATTGCAGGTTGGCAAGTGGGCTGATGGGGTCCGCCCTCCTCACTGCT CCACAGGATGGTGGTGGCATTGCAGGTTGGCAGGTGGGCTGATGGGGTCCGCCCTCCTCACTGCT T C P3H4 Ensembl:ENSG00000141696 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1221171357 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_489166,Human_RBP_ID_4426156,Human_RBP_ID_8817731,Human_RBP_ID_17654181,Human_RBP_ID_18292195,Human_RBP_ID_26450557,Human_RBP_ID_27253865 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 50479 RMVar_ID_50479 Human_SNP_ID_624469001 A-to-I Human chr17 - 41802369 41802369 41802369 TCGTAGCTGAGGCAGGAGAATCGCCTGAACCCAGGAGGCGGAGCTTGCAGTGAGCCGAGATCGTG TCGTAGCTGAGGCAGGAGAATCGCCTGAACCCGGGAGGCGGAGCTTGCAGTGAGCCGAGATCGTG T C P3H4 Ensembl:ENSG00000141696 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1242704990 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_489170,Human_RBP_ID_13002118 Human_Splice_Rec_1816660 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 50480 RMVar_ID_50480 Human_SNP_ID_624469013 A-to-I Human chr17 - 41802421 41802421 41802421 TCTCTACTAAAAAATACAAAAATTAGCCAGGCATGGTGGCACACACCTGTAATCGTAGCTGAGGC TCTCTACTAAAAAATACAAAAATTAGCCAGGCGTGGTGGCACACACCTGTAATCGTAGCTGAGGC T C P3H4 Ensembl:ENSG00000141696 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1034450400 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1816660 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 50481 RMVar_ID_50481 Human_SNP_ID_624469108 A-to-I Human chr17 - 41802716 41802706 41802717 GAGACCTCCGTCTCTACTAAAATACATAAATTAGCCGGGTGTGGTGGCAGGCGCCTGAAATCCCA GAGACCTCCGTCTCTACTAAAATACATAAAT___________GGTGGCAGGCGCCTGAAATCCCA CACACCCGGCTA C P3H4 Ensembl:ENSG00000141696 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1163372729 Functional Loss DEL dbSNP153 32..42 33 - - - Human_RBP_ID_22960835 Human_Splice_Rec_1816659 Human_miRNA_ID_3115230 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 50482 RMVar_ID_50482 Human_SNP_ID_624476065 A-to-I Human chr17 - 41825981 41825981 41825981 CCGGCCAATTTTTGTAGAGATGGGCTTTTGCCATGTTGCCTGGGCTGGTCTCAAACTCTTGGGCT CCGGCCAATTTTTGTAGAGATGGGCTTTTGCCGTGTTGCCTGGGCTGGTCTCAAACTCTTGGGCT T C NT5C3B Ensembl:ENSG00000141698 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs190208964 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13002415,Human_RBP_ID_25282912 50483 RMVar_ID_50483 Human_SNP_ID_624476083 A-to-I Human chr17 - 41826055 41826055 41826055 ATTTCCTGGGCTCAAGTGATCCTTTCTGCCTCAGTCTCCCGAGTAGCTGGGACTACAGGCACCCA ATTTCCTGGGCTCAAGTGATCCTTTCTGCCTCCGTCTCCCGAGTAGCTGGGACTACAGGCACCCA T G NT5C3B Ensembl:ENSG00000141698 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1450808546 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13002424 50484 RMVar_ID_50484 Human_SNP_ID_624476164 A-to-I Human chr17 - 41826246 41826246 41826246 GCACTTCAGCCTACGCAGCAGAGTGAGATCCTATCTCAAAAAAGAAAGAAAGAAAGAAAGAAAGA GCACTTCAGCCTACGCAGCAGAGTGAGATCCTGTCTCAAAAAAGAAAGAAAGAAAGAAAGAAAGA T C NT5C3B Ensembl:ENSG00000141698 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1445923829 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17565912,Human_RBP_ID_25342057 50485 RMVar_ID_50485 Human_SNP_ID_624476172 A-to-I Human chr17 - 41826286 41826286 41826286 CCAGGAGGTTGAAGCTGCAGTGAGCCAAGATTATGCCACTGCACTTCAGCCTACGCAGCAGAGTG CCAGGAGGTTGAAGCTGCAGTGAGCCAAGATTTTGCCACTGCACTTCAGCCTACGCAGCAGAGTG T A NT5C3B Ensembl:ENSG00000141698 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1256433489 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17565912 50486 RMVar_ID_50486 Human_SNP_ID_624476183 A-to-I Human chr17 - 41826362 41826356 41826363 AACAATTAGCTGGGTGTGGTTAGCATGCCTGTAGTTCTAGTTACTCAGGAGGCTGAGGCAGGAAG AACAATTAGCTGGGTGTGGTTAGCATGCCTG_______AGTTACTCAGGAGGCTGAGGCAGGAAG TAGAACTA T NT5C3B Ensembl:ENSG00000141698 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1312278859 Functional Loss DEL dbSNP153 32..38 33 - - - 50487 RMVar_ID_50487 Human_SNP_ID_624476205 A-to-I Human chr17 - 41826442 41826442 41826442 AGGGCAGGGGGATCACTTGAGGCCAGGAGTTTAAGACCAGCCTGGGCAACATAGTGAGACCCTGT AGGGCAGGGGGATCACTTGAGGCCAGGAGTTTGAGACCAGCCTGGGCAACATAGTGAGACCCTGT T C NT5C3B Ensembl:ENSG00000141698 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs966824715 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25282916 50488 RMVar_ID_50488 Human_SNP_ID_624476321 A-to-I Human chr17 - 41826924 41826924 41826924 GCCATCTTGGCTTACTGCAACTTCCACCTCCCAGGTTCAAGTGATTCTTCTGCCTCAGGCAGCTG GCCATCTTGGCTTACTGCAACTTCCACCTCCCTGGTTCAAGTGATTCTTCTGCCTCAGGCAGCTG T A NT5C3B Ensembl:ENSG00000141698 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1355246285 Functional Loss SNV dbSNP153 33..33 33 - - - 50489 RMVar_ID_50489 Human_SNP_ID_624476322 A-to-I Human chr17 - 41826924 41826924 41826924 GCCATCTTGGCTTACTGCAACTTCCACCTCCCAGGTTCAAGTGATTCTTCTGCCTCAGGCAGCTG GCCATCTTGGCTTACTGCAACTTCCACCTCCCGGGTTCAAGTGATTCTTCTGCCTCAGGCAGCTG T C NT5C3B Ensembl:ENSG00000141698 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1355246285 Functional Loss SNV dbSNP153 33..33 33 - - - 50490 RMVar_ID_50490 Human_SNP_ID_624482096 A-to-I Human chr17 - 41848921 41848921 41848921 GCGGTTTGTTTATTACACTTGTAGGGCTTTTTATCTTACTCAGTGACCATCACTACGAATGTCTT GCGGTTTGTTTATTACACTTGTAGGGCTTTTTGTCTTACTCAGTGACCATCACTACGAATGTCTT T C AC125257.1,KLHL11 Ensembl:ENSG00000259623,Ensembl:ENSG00000178502 lincRNA,Protein coding exon,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4796616 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1011399,Human_RBP_ID_8817749,Human_RBP_ID_9287469,Human_RBP_ID_18292214,Human_RBP_ID_22389582,Human_RBP_ID_26460543,Human_RBP_ID_27665104 Human_miRNA_ID_3204031 GWAS_ID_6429,GWAS_ID_6430,GWAS_ID_6431,GWAS_ID_6432,GWAS_ID_6433,GWAS_ID_6434,GWAS_ID_6435,GWAS_ID_6436,GWAS_ID_6437,GWAS_ID_6438,GWAS_ID_6439,GWAS_ID_6440,GWAS_ID_6441,GWAS_ID_6442,GWAS_ID_6443,GWAS_ID_6444,GWAS_ID_6445,GWAS_ID_6446,GWAS_ID_6447,GWAS_ID_6448,GWAS_ID_6449,GWAS_ID_6450,GWAS_ID_6451,GWAS_ID_6452,GWAS_ID_6453,GWAS_ID_6454,GWAS_ID_6455,GWAS_ID_6456,GWAS_ID_6457,GWAS_ID_6458,GWAS_ID_6459,GWAS_ID_6460,GWAS_ID_6461,GWAS_ID_6462,GWAS_ID_6463,GWAS_ID_6464,GWAS_ID_6465,GWAS_ID_6466,GWAS_ID_6467,GWAS_ID_6468,GWAS_ID_6469,GWAS_ID_6470,GWAS_ID_6471,GWAS_ID_6472,GWAS_ID_6473,GWAS_ID_6474,GWAS_ID_6475,GWAS_ID_6476,GWAS_ID_6477,GWAS_ID_6478,GWAS_ID_6479,GWAS_ID_6480,GWAS_ID_6481,GWAS_ID_6482,GWAS_ID_6483,GWAS_ID_6484,GWAS_ID_6485,GWAS_ID_6486,GWAS_ID_6487,GWAS_ID_6488,GWAS_ID_6489,GWAS_ID_6490,GWAS_ID_6491,GWAS_ID_6492,GWAS_ID_6493,GWAS_ID_6494,GWAS_ID_6495,GWAS_ID_6496,GWAS_ID_6497,GWAS_ID_6498,GWAS_ID_6499,GWAS_ID_6500,GWAS_ID_6501,GWAS_ID_6502,GWAS_ID_6503 50491 RMVar_ID_50491 Human_SNP_ID_624482504 A-to-I Human chr17 - 41851113 41851113 41851113 CACCTGTCCAATGATTTATCCTGTTTCTTAAGAACTGTCTTTACCTTCTTAGACATTTTGTCATA CACCTGTCCAATGATTTATCCTGTTTCTTAAGGACTGTCTTTACCTTCTTAGACATTTTGTCATA T C AC125257.1,KLHL11 Ensembl:ENSG00000259623,Ensembl:ENSG00000178502 lincRNA,Protein coding exon,3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4796722 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5188972,Human_RBP_ID_6594090,Human_RBP_ID_8817801,Human_RBP_ID_22389586,Human_RBP_ID_26460550 GWAS_ID_6504,GWAS_ID_6505,GWAS_ID_6506,GWAS_ID_6507,GWAS_ID_6508,GWAS_ID_6509,GWAS_ID_6510,GWAS_ID_6511,GWAS_ID_6512,GWAS_ID_6513,GWAS_ID_6514,GWAS_ID_6515,GWAS_ID_6516,GWAS_ID_6517,GWAS_ID_6518,GWAS_ID_6519,GWAS_ID_6520,GWAS_ID_6521,GWAS_ID_6522,GWAS_ID_6523,GWAS_ID_6524,GWAS_ID_6525,GWAS_ID_6526,GWAS_ID_6527,GWAS_ID_6528,GWAS_ID_6529,GWAS_ID_6530,GWAS_ID_6531,GWAS_ID_6532,GWAS_ID_6533,GWAS_ID_6534,GWAS_ID_6535,GWAS_ID_6536,GWAS_ID_6537,GWAS_ID_6538,GWAS_ID_6539,GWAS_ID_6540,GWAS_ID_6541,GWAS_ID_6542,GWAS_ID_6543,GWAS_ID_6544,GWAS_ID_6545,GWAS_ID_6546,GWAS_ID_6547,GWAS_ID_6548,GWAS_ID_6549,GWAS_ID_6550,GWAS_ID_6551,GWAS_ID_6552,GWAS_ID_6553,GWAS_ID_6554,GWAS_ID_6555,GWAS_ID_6556,GWAS_ID_6557,GWAS_ID_6558,GWAS_ID_6559,GWAS_ID_6560,GWAS_ID_6561,GWAS_ID_6562,GWAS_ID_6563,GWAS_ID_6564,GWAS_ID_6565,GWAS_ID_6566,GWAS_ID_6567,GWAS_ID_6568,GWAS_ID_6569,GWAS_ID_6570,GWAS_ID_6571,GWAS_ID_6572,GWAS_ID_6573,GWAS_ID_6574,GWAS_ID_6575,GWAS_ID_6576,GWAS_ID_6577,GWAS_ID_6578 50492 RMVar_ID_50492 Human_SNP_ID_624482551 A-to-I Human chr17 - 41851360 41851360 41851360 TGACCTCGTGATCCGCCCACCTCAGCCTCTCAAAGCGCTGGGATTACAGGCATGAGCCACCATGC TGACCTCGTGATCCGCCCACCTCAGCCTCTCAGAGCGCTGGGATTACAGGCATGAGCCACCATGC T C AC125257.1,KLHL11 Ensembl:ENSG00000259623,Ensembl:ENSG00000178502 lincRNA,Protein coding exon,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs937534606 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3548144,Human_RBP_ID_13002762 50493 RMVar_ID_50493 Human_SNP_ID_624482637 A-to-I Human chr17 - 41851723 41851723 41851723 TTTTGTATTTTTGGTAGAGATGGGGTTTCTCCATGTTGCCGAGGCTGGTCTCCAACTCCTGGGCT TTTTGTATTTTTGGTAGAGATGGGGTTTCTCCGTGTTGCCGAGGCTGGTCTCCAACTCCTGGGCT T C KLHL11 Ensembl:ENSG00000178502 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1230883202 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6594109,Human_RBP_ID_13002773 50494 RMVar_ID_50494 Human_SNP_ID_624482743 A-to-I Human chr17 - 41852131 41852131 41852131 GCACGTGCCTGTAGTCCTTCCTACTTGAAGCCAAGGTGGGAGGATCACCAGAGCCTGGGAAGGTT GCACGTGCCTGTAGTCCTTCCTACTTGAAGCCGAGGTGGGAGGATCACCAGAGCCTGGGAAGGTT T C KLHL11 Ensembl:ENSG00000178502 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs976989623 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6594128,Human_RBP_ID_8817815,Human_RBP_ID_9287498,Human_RBP_ID_13002804 50495 RMVar_ID_50495 Human_SNP_ID_624482755 A-to-I Human chr17 - 41852216 41852215 41852217 GCCCAAGAGTTCAAGACCAGCCTGGGAAACATAGCAAGATCCTGTCTCTACAAAAAGTAGAAAAA GCCCAAGAGTTCAAGACCAGCCTGGGAAACA__GCAAGATCCTGTCTCTACAAAAAGTAGAAAAA CTA C KLHL11 Ensembl:ENSG00000178502 Protein coding 3'UTR GSE38233;GSE100210;GSE107867;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,frontal_cortex;ASD brains,temporal_cortex - 24183664,29129909,30559470,30559470 RNA-Seq:(High) rs1316820859 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_26460551 50496 RMVar_ID_50496 Human_SNP_ID_624482768 A-to-I Human chr17 - 41852283 41852283 41852283 GCTGGGCACGGTGGCTCATGACTGTAATCCCAACACTTTGGAGGAGGCTGAGGTGGGCAGATTTT GCTGGGCACGGTGGCTCATGACTGTAATCCCAGCACTTTGGAGGAGGCTGAGGTGGGCAGATTTT T C KLHL11 Ensembl:ENSG00000178502 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs111618590 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6594135,Human_RBP_ID_13002808 50497 RMVar_ID_50497 Human_SNP_ID_624482779 A-to-I Human chr17 - 41852308 41852308 41852308 AATTTTGGCTTTTAAAGGTTTATGGGCTGGGCACGGTGGCTCATGACTGTAATCCCAACACTTTG AATTTTGGCTTTTAAAGGTTTATGGGCTGGGCGCGGTGGCTCATGACTGTAATCCCAACACTTTG T C KLHL11 Ensembl:ENSG00000178502 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs977502107 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4426539,Human_RBP_ID_6594135,Human_RBP_ID_13002809 50498 RMVar_ID_50498 Human_SNP_ID_624482820 A-to-I Human chr17 - 41852534 41852534 41852534 CGCCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGTGCCCAGTCCATTATT CGCCCGCCTCAGCCTCCCAAAGTGCTGGGATTGCAGGCATGAGCCACCGTGCCCAGTCCATTATT T C KLHL11 Ensembl:ENSG00000178502 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1231989850 Functional Loss SNV dbSNP153 33..33 33 - - - 50499 RMVar_ID_50499 Human_SNP_ID_624482840 A-to-I Human chr17 - 41852608 41852608 41852608 TTTTGTGCTTTTAGTAGAGACAGGGTTTCACCATGTTGACCAGGCTGGTCTTGAACTCCTGACCT TTTTGTGCTTTTAGTAGAGACAGGGTTTCACCGTGTTGACCAGGCTGGTCTTGAACTCCTGACCT T C KLHL11 Ensembl:ENSG00000178502 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1468691927 Functional Loss SNV dbSNP153 33..33 33 - - - 50500 RMVar_ID_50500 Human_SNP_ID_624482841 A-to-I Human chr17 - 41852611 41852611 41852611 AATTTTTGTGCTTTTAGTAGAGACAGGGTTTCACCATGTTGACCAGGCTGGTCTTGAACTCCTGA AATTTTTGTGCTTTTAGTAGAGACAGGGTTTCGCCATGTTGACCAGGCTGGTCTTGAACTCCTGA T C KLHL11 Ensembl:ENSG00000178502 Protein coding 3'UTR GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1251759935 Functional Loss SNV dbSNP153 33..33 33 - - - 50501 RMVar_ID_50501 Human_SNP_ID_624488976 A-to-I Human chr17 - 41875092 41875092 41875092 CGCCTGCCTTGGTCTCCCAAAGTGCTGAGATTACAGGCATAAGCCACTGTGCCCTGCCCCATTAC CGCCTGCCTTGGTCTCCCAAAGTGCTGAGATTGCAGGCATAAGCCACTGTGCCCTGCCCCATTAC T C ACLY Ensembl:ENSG00000131473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1485253899 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_65435,RMVar_hsa_circ_10775,RMVar_hsa_circ_343390,RMVar_hsa_circ_366393,RMVar_hsa_circ_345092,RMVar_hsa_circ_84078,RMVar_hsa_circ_328213,RMVar_hsa_circ_11177,RMVar_hsa_circ_184238,RMVar_hsa_circ_288677,RMVar_hsa_circ_347692 50502 RMVar_ID_50502 Human_SNP_ID_624488996 A-to-I Human chr17 - 41875184 41875184 41875184 CACCACGCCCAGCTAATTTTTGTAGTTTCAATAGATAATGGGGTTTCACCATGTTGGCCAGGCTG CACCACGCCCAGCTAATTTTTGTAGTTTCAATGGATAATGGGGTTTCACCATGTTGGCCAGGCTG T C ACLY Ensembl:ENSG00000131473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1165483772 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_65435,RMVar_hsa_circ_10775,RMVar_hsa_circ_343390,RMVar_hsa_circ_366393,RMVar_hsa_circ_345092,RMVar_hsa_circ_84078,RMVar_hsa_circ_328213,RMVar_hsa_circ_11177,RMVar_hsa_circ_184238,RMVar_hsa_circ_288677,RMVar_hsa_circ_347692 50503 RMVar_ID_50503 Human_SNP_ID_624489006 A-to-I Human chr17 - 41875237 41875237 41875237 CAAGCGATTCTCCTGCCTTAGCCTCCCGAGTAACTGGGGTTACAGACACATACCACCACGCCCAG CAAGCGATTCTCCTGCCTTAGCCTCCCGAGTAGCTGGGGTTACAGACACATACCACCACGCCCAG T C ACLY Ensembl:ENSG00000131473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1555625849 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_65435,RMVar_hsa_circ_10775,RMVar_hsa_circ_343390,RMVar_hsa_circ_366393,RMVar_hsa_circ_345092,RMVar_hsa_circ_84078,RMVar_hsa_circ_328213,RMVar_hsa_circ_11177,RMVar_hsa_circ_184238,RMVar_hsa_circ_288677,RMVar_hsa_circ_347692 50504 RMVar_ID_50504 Human_SNP_ID_624490858 A-to-I Human chr17 - 41881328 41881328 41881328 GCCTCTGCCTCCCTGGTTTAAGCAATTCTCCTACTTCAGTCTCCCAAGTAGCTGGGATAACAGCC GCCTCTGCCTCCCTGGTTTAAGCAATTCTCCTGCTTCAGTCTCCCAAGTAGCTGGGATAACAGCC T C ACLY Ensembl:ENSG00000131473 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1352821028 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12047,RMVar_hsa_circ_65435,RMVar_hsa_circ_343390,RMVar_hsa_circ_366393,RMVar_hsa_circ_345092,RMVar_hsa_circ_328213,RMVar_hsa_circ_298107,RMVar_hsa_circ_11177,RMVar_hsa_circ_288677,RMVar_hsa_circ_347692,RMVar_hsa_circ_323417,RMVar_hsa_circ_342503,RMVar_hsa_circ_43347,RMVar_hsa_circ_48177,RMVar_hsa_circ_26428,RMVar_hsa_circ_21398 50505 RMVar_ID_50505 Human_SNP_ID_624491767 A-to-I Human chr17 - 41884771 41884771 41884771 GCGATCCTCCCGTCTCAGCCACCTGAGTAGCTAGGACTGTACAGGCGCCCACGACCACACCTGGC GCGATCCTCCCGTCTCAGCCACCTGAGTAGCTTGGACTGTACAGGCGCCCACGACCACACCTGGC T A ACLY Ensembl:ENSG00000131473 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223978649 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13003177 RMVar_hsa_circ_12047,RMVar_hsa_circ_65435,RMVar_hsa_circ_343390,RMVar_hsa_circ_366393,RMVar_hsa_circ_328213,RMVar_hsa_circ_298107,RMVar_hsa_circ_11177,RMVar_hsa_circ_347692,RMVar_hsa_circ_342503,RMVar_hsa_circ_43347,RMVar_hsa_circ_48177,RMVar_hsa_circ_26428,RMVar_hsa_circ_71828,RMVar_hsa_circ_12315,RMVar_hsa_circ_21398,RMVar_hsa_circ_377651,RMVar_hsa_circ_44854,RMVar_hsa_circ_272915,RMVar_hsa_circ_88232,RMVar_hsa_circ_184241,RMVar_hsa_circ_20919 50506 RMVar_ID_50506 Human_SNP_ID_624491768 A-to-I Human chr17 - 41884771 41884771 41884771 GCGATCCTCCCGTCTCAGCCACCTGAGTAGCTAGGACTGTACAGGCGCCCACGACCACACCTGGC GCGATCCTCCCGTCTCAGCCACCTGAGTAGCTGGGACTGTACAGGCGCCCACGACCACACCTGGC T C ACLY Ensembl:ENSG00000131473 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223978649 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13003177 RMVar_hsa_circ_12047,RMVar_hsa_circ_65435,RMVar_hsa_circ_343390,RMVar_hsa_circ_366393,RMVar_hsa_circ_328213,RMVar_hsa_circ_298107,RMVar_hsa_circ_11177,RMVar_hsa_circ_347692,RMVar_hsa_circ_342503,RMVar_hsa_circ_43347,RMVar_hsa_circ_48177,RMVar_hsa_circ_26428,RMVar_hsa_circ_71828,RMVar_hsa_circ_12315,RMVar_hsa_circ_21398,RMVar_hsa_circ_377651,RMVar_hsa_circ_44854,RMVar_hsa_circ_272915,RMVar_hsa_circ_88232,RMVar_hsa_circ_184241,RMVar_hsa_circ_20919 50507 RMVar_ID_50507 Human_SNP_ID_624492807 A-to-I Human chr17 - 41888743 41888743 41888743 AGTGATGCAATCATGCAACTCACTGTAGCCTCAACCTCCTGGGTTCAATTGATCCTCCTACCGGG AGTGATGCAATCATGCAACTCACTGTAGCCTCCACCTCCTGGGTTCAATTGATCCTCCTACCGGG T G ACLY Ensembl:ENSG00000131473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs973802994 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_65435,RMVar_hsa_circ_366393,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_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_280105,RMVar_hsa_circ_184245,RMVar_hsa_circ_184246 50508 RMVar_ID_50508 Human_SNP_ID_624492826 A-to-I Human chr17 - 41888862 41888862 41888862 TGCCCACCTTGGCCTTGCAGATTGCTGGGATTATAGATGTGAGCCACCGCGCACAGCCAGGGGTT TGCCCACCTTGGCCTTGCAGATTGCTGGGATTGTAGATGTGAGCCACCGCGCACAGCCAGGGGTT T C ACLY Ensembl:ENSG00000131473 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1253708914 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_65435,RMVar_hsa_circ_366393,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_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_280105,RMVar_hsa_circ_184245,RMVar_hsa_circ_184246 50509 RMVar_ID_50509 Human_SNP_ID_624496354 A-to-I Human chr17 - 41902306 41902306 41902306 GGGAGGATGAGACAGGAGAATCGCTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCCGAGCTCACA GGGAGGATGAGACAGGAGAATCGCTTGAACCCGGGAGGCAGAGGTTGCAGTGAGCCGAGCTCACA T C ACLY Ensembl:ENSG00000131473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs9908748 Functional Loss SNV dbSNP153 33..33 33 - - - 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_48732,RMVar_hsa_circ_367772 50510 RMVar_ID_50510 Human_SNP_ID_624496527 A-to-I Human chr17 - 41903064 41903064 41903064 AAGTGAGAGGCTGGGCGTGGTGGCTTATAACTATAATTCTAGCACTTTGAGAGGCTGAGGCAGGC AAGTGAGAGGCTGGGCGTGGTGGCTTATAACTGTAATTCTAGCACTTTGAGAGGCTGAGGCAGGC T C ACLY Ensembl:ENSG00000131473 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1259019836 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13003548 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_48732,RMVar_hsa_circ_367772 50511 RMVar_ID_50511 Human_SNP_ID_624496786 A-to-I Human chr17 - 41904057 41904057 41904057 GCTGGAGTGCAATGGCACGATCTCAGCTCACTACAGCCTCTGCCTCCTGGGTTCAAGTGATTCTC GCTGGAGTGCAATGGCACGATCTCAGCTCACTGCAGCCTCTGCCTCCTGGGTTCAAGTGATTCTC T C ACLY Ensembl:ENSG00000131473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1293937426 Functional Loss SNV dbSNP153 33..33 33 - - - 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_48732,RMVar_hsa_circ_367772 50512 RMVar_ID_50512 Human_SNP_ID_624496796 A-to-I Human chr17 - 41904078 41904078 41904078 AGTTTCACTCTTGTTGTTGAGGCTGGAGTGCAATGGCACGATCTCAGCTCACTACAGCCTCTGCC AGTTTCACTCTTGTTGTTGAGGCTGGAGTGCAGTGGCACGATCTCAGCTCACTACAGCCTCTGCC T C ACLY Ensembl:ENSG00000131473 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1419420752 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1181881,Human_RBP_ID_17566468,Human_RBP_ID_20213800,Human_RBP_ID_22804425 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_48732,RMVar_hsa_circ_367772 50513 RMVar_ID_50513 Human_SNP_ID_624499065 A-to-I Human chr17 - 41912479 41912479 41912479 AACGTCGTGGAAAACTTGGTCTCGTTGGGGTCAACCTCACTCTGGATGGGGTCAAGTCCTGGCTG AACGTCGTGGAAAACTTGGTCTCGTTGGGGTCGACCTCACTCTGGATGGGGTCAAGTCCTGGCTG T C ACLY Ensembl:ENSG00000131473 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1058875 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_47885,Human_RBP_ID_1008125,Human_RBP_ID_1533797,Human_RBP_ID_1858082,Human_RBP_ID_3523150,Human_RBP_ID_8452336,Human_RBP_ID_8817970,Human_RBP_ID_9375983,Human_RBP_ID_13003812,Human_RBP_ID_17491261,Human_RBP_ID_18420495,Human_RBP_ID_18697596,Human_RBP_ID_18988437,Human_RBP_ID_22443650,Human_RBP_ID_22959593,Human_RBP_ID_26769310,Human_RBP_ID_26961115,Human_RBP_ID_27452280 Human_Splice_Rec_1816956,Human_Splice_Rec_1816957,Human_Splice_Rec_1817012,Human_Splice_Rec_1817013,Human_Splice_Rec_1817068,Human_Splice_Rec_1817069,Human_Splice_Rec_1817122,Human_Splice_Rec_1817123,Human_Splice_Rec_1817162,Human_Splice_Rec_1817163,Human_Splice_Rec_1817246,Human_Splice_Rec_1817247 Human_miRNA_ID_2007611,Human_miRNA_ID_2825845,Human_miRNA_ID_2859818 RMVar_hsa_circ_43347,RMVar_hsa_circ_113752,RMVar_hsa_circ_184244,RMVar_hsa_circ_99355,RMVar_hsa_circ_184247,RMVar_hsa_circ_122769,RMVar_hsa_circ_12759,RMVar_hsa_circ_184260,RMVar_hsa_circ_90670,RMVar_hsa_circ_11163,RMVar_hsa_circ_184263,RMVar_hsa_circ_36161,RMVar_hsa_circ_289458,RMVar_hsa_circ_71825,RMVar_hsa_circ_331178,RMVar_hsa_circ_184264 50514 RMVar_ID_50514 Human_SNP_ID_624499066 A-to-I Human chr17 - 41912479 41912479 41912479 AACGTCGTGGAAAACTTGGTCTCGTTGGGGTCAACCTCACTCTGGATGGGGTCAAGTCCTGGCTG AACGTCGTGGAAAACTTGGTCTCGTTGGGGTCCACCTCACTCTGGATGGGGTCAAGTCCTGGCTG T G ACLY Ensembl:ENSG00000131473 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1058875 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_47885,Human_RBP_ID_1008125,Human_RBP_ID_1533797,Human_RBP_ID_1858082,Human_RBP_ID_3523150,Human_RBP_ID_8452336,Human_RBP_ID_8817970,Human_RBP_ID_9375983,Human_RBP_ID_13003812,Human_RBP_ID_17491261,Human_RBP_ID_18420495,Human_RBP_ID_18697596,Human_RBP_ID_18988437,Human_RBP_ID_22443650,Human_RBP_ID_22959593,Human_RBP_ID_26769310,Human_RBP_ID_26961115,Human_RBP_ID_27452280 Human_Splice_Rec_1816956,Human_Splice_Rec_1816957,Human_Splice_Rec_1817012,Human_Splice_Rec_1817013,Human_Splice_Rec_1817068,Human_Splice_Rec_1817069,Human_Splice_Rec_1817122,Human_Splice_Rec_1817123,Human_Splice_Rec_1817162,Human_Splice_Rec_1817163,Human_Splice_Rec_1817246,Human_Splice_Rec_1817247 Human_miRNA_ID_2007611,Human_miRNA_ID_2825845,Human_miRNA_ID_2859818 RMVar_hsa_circ_43347,RMVar_hsa_circ_113752,RMVar_hsa_circ_184244,RMVar_hsa_circ_99355,RMVar_hsa_circ_184247,RMVar_hsa_circ_122769,RMVar_hsa_circ_12759,RMVar_hsa_circ_184260,RMVar_hsa_circ_90670,RMVar_hsa_circ_11163,RMVar_hsa_circ_184263,RMVar_hsa_circ_36161,RMVar_hsa_circ_289458,RMVar_hsa_circ_71825,RMVar_hsa_circ_331178,RMVar_hsa_circ_184264 50515 RMVar_ID_50515 Human_SNP_ID_624508964 A-to-I Human chr17 + 41952274 41952274 41952274 CTTGTAATCCAAGCTGCTCGGGAGGCTGAGGCAGGAGAGTTGCTTGAACCTGGGAGGCGGAGGTT CTTGTAATCCAAGCTGCTCGGGAGGCTGAGGCCGGAGAGTTGCTTGAACCTGGGAGGCGGAGGTT A C TTC25 Ensembl:ENSG00000204815 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1288947174 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_332207,RMVar_hsa_circ_52893 50516 RMVar_ID_50516 Human_SNP_ID_624517167 A-to-I Human chr17 - 41982793 41982792 41982793 ACCACGCCTGGCTAATTTTTTGTATTTTTAGTAGGGATGGGGTTTCACCATGTTGGACAGGCTAG ACCACGCCTGGCTAATTTTTTGTATTTTTAGT_GGGATGGGGTTTCACCATGTTGGACAGGCTAG CT C DNAJC7 Ensembl:ENSG00000168259 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1208103115 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_25283352 RMVar_hsa_circ_60760,RMVar_hsa_circ_64204,RMVar_hsa_circ_30694,RMVar_hsa_circ_184271,RMVar_hsa_circ_343362,RMVar_hsa_circ_346770,RMVar_hsa_circ_114964,RMVar_hsa_circ_57915 50517 RMVar_ID_50517 Human_SNP_ID_624517168 A-to-I Human chr17 - 41982802 41982802 41982802 GCACATGGTACCACGCCTGGCTAATTTTTTGTATTTTTAGTAGGGATGGGGTTTCACCATGTTGG GCACATGGTACCACGCCTGGCTAATTTTTTGTGTTTTTAGTAGGGATGGGGTTTCACCATGTTGG T C DNAJC7 Ensembl:ENSG00000168259 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1352992971 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_60760,RMVar_hsa_circ_64204,RMVar_hsa_circ_30694,RMVar_hsa_circ_184271,RMVar_hsa_circ_343362,RMVar_hsa_circ_346770,RMVar_hsa_circ_114964,RMVar_hsa_circ_57915 50518 RMVar_ID_50518 Human_SNP_ID_624518077 A-to-I Human chr17 - 41986222 41986222 41986222 AGCTGAGATTACCGGCGCATGTCACCACACCCAGCAAATTTTTGTATTTTTATTGGAGATGGGGT AGCTGAGATTACCGGCGCATGTCACCACACCCGGCAAATTTTTGTATTTTTATTGGAGATGGGGT T C DNAJC7 Ensembl:ENSG00000168259 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1210499144 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_30694,RMVar_hsa_circ_184271,RMVar_hsa_circ_343362,RMVar_hsa_circ_114964,RMVar_hsa_circ_57915 50519 RMVar_ID_50519 Human_SNP_ID_624519370 A-to-I Human chr17 - 41991863 41991863 41991863 CAACCTGGGCAACTTATTGAGACCCTGTCTCTACAGATAATTTAAAATTTTAGCTGAGTGTGGTG CAACCTGGGCAACTTATTGAGACCCTGTCTCTGCAGATAATTTAAAATTTTAGCTGAGTGTGGTG T C DNAJC7 Ensembl:ENSG00000168259 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1226120387 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_30694,RMVar_hsa_circ_184271,RMVar_hsa_circ_114964,RMVar_hsa_circ_57915 50520 RMVar_ID_50520 Human_SNP_ID_624519386 A-to-I Human chr17 - 41991918 41991918 41991918 CCAGCACTTTGGGAGGCCAAGGCAGGAGGATCACTTGAGGCGAGGAGTTCGAGACCAACCTGGGC CCAGCACTTTGGGAGGCCAAGGCAGGAGGATCGCTTGAGGCGAGGAGTTCGAGACCAACCTGGGC T C DNAJC7 Ensembl:ENSG00000168259 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4378665 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_6579,GWAS_ID_6580,GWAS_ID_6581,GWAS_ID_6582,GWAS_ID_6583,GWAS_ID_6584,GWAS_ID_6585,GWAS_ID_6586,GWAS_ID_6587 RMVar_hsa_circ_30694,RMVar_hsa_circ_184271,RMVar_hsa_circ_114964,RMVar_hsa_circ_57915 50521 RMVar_ID_50521 Human_SNP_ID_624520931 A-to-I Human chr17 - 41997923 41997923 41997923 AGGAGGCGGAGGATGCAGTGAGCAGAGATCATACCACTGCAGTCCAGCGTGGGCAACAGAGCCAG AGGAGGCGGAGGATGCAGTGAGCAGAGATCATGCCACTGCAGTCCAGCGTGGGCAACAGAGCCAG T C DNAJC7 Ensembl:ENSG00000168259 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs529500193 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_30694,RMVar_hsa_circ_21352,RMVar_hsa_circ_57915,RMVar_hsa_circ_276235,RMVar_hsa_circ_113442,RMVar_hsa_circ_184275,RMVar_hsa_circ_184276,RMVar_hsa_circ_278318,RMVar_hsa_circ_322239,RMVar_hsa_circ_44578 50522 RMVar_ID_50522 Human_SNP_ID_624520932 A-to-I Human chr17 - 41997925 41997925 41997925 CCAGGAGGCGGAGGATGCAGTGAGCAGAGATCATACCACTGCAGTCCAGCGTGGGCAACAGAGCC CCAGGAGGCGGAGGATGCAGTGAGCAGAGATCGTACCACTGCAGTCCAGCGTGGGCAACAGAGCC T C DNAJC7 Ensembl:ENSG00000168259 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1193498015 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_30694,RMVar_hsa_circ_21352,RMVar_hsa_circ_57915,RMVar_hsa_circ_276235,RMVar_hsa_circ_113442,RMVar_hsa_circ_184275,RMVar_hsa_circ_184276,RMVar_hsa_circ_278318,RMVar_hsa_circ_322239,RMVar_hsa_circ_44578 50523 RMVar_ID_50523 Human_SNP_ID_624520933 A-to-I Human chr17 - 41997925 41997925 41997925 CCAGGAGGCGGAGGATGCAGTGAGCAGAGATCATACCACTGCAGTCCAGCGTGGGCAACAGAGCC CCAGGAGGCGGAGGATGCAGTGAGCAGAGATCCTACCACTGCAGTCCAGCGTGGGCAACAGAGCC T G DNAJC7 Ensembl:ENSG00000168259 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1193498015 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_30694,RMVar_hsa_circ_21352,RMVar_hsa_circ_57915,RMVar_hsa_circ_276235,RMVar_hsa_circ_113442,RMVar_hsa_circ_184275,RMVar_hsa_circ_184276,RMVar_hsa_circ_278318,RMVar_hsa_circ_322239,RMVar_hsa_circ_44578 50524 RMVar_ID_50524 Human_SNP_ID_624521131 A-to-I Human chr17 - 41998935 41998935 41998935 GCGATCCTCCTACCTTGGCCTCCCAAAGTGCTAGAATTACAGGGATGTGCCACCATCCCCAGCTG GCGATCCTCCTACCTTGGCCTCCCAAAGTGCTTGAATTACAGGGATGTGCCACCATCCCCAGCTG T A DNAJC7 Ensembl:ENSG00000168259 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1204934828 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_30694,RMVar_hsa_circ_21352,RMVar_hsa_circ_57915,RMVar_hsa_circ_276235,RMVar_hsa_circ_113442,RMVar_hsa_circ_184275,RMVar_hsa_circ_184276,RMVar_hsa_circ_278318,RMVar_hsa_circ_322239,RMVar_hsa_circ_44578 50525 RMVar_ID_50525 Human_SNP_ID_624522309 A-to-I Human chr17 - 42004058 42004058 42004058 CCCAGCTACTCGGGAGGCTAAGGCGAGAGAACACTTGAACCCAGGAGGCAGAGGCTGCAGTGAAC CCCAGCTACTCGGGAGGCTAAGGCGAGAGAACCCTTGAACCCAGGAGGCAGAGGCTGCAGTGAAC T G DNAJC7 Ensembl:ENSG00000168259 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs377141221 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13005422 50526 RMVar_ID_50526 Human_SNP_ID_624522470 A-to-I Human chr17 - 42004854 42004853 42004855 TGCCCAGCTAATTTTTAAATTTTTGTAGAGACAGAGTCTCCCTGTGTTTTCCAGGCTGTTCTCAA TGCCCAGCTAATTTTTAAATTTTTGTAGAGA__GAGTCTCCCTGTGTTTTCCAGGCTGTTCTCAA CTG C DNAJC7 Ensembl:ENSG00000168259 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs565216085 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_13005446 50527 RMVar_ID_50527 Human_SNP_ID_624522485 A-to-I Human chr17 - 42004942 42004942 42004942 CAGCTCGTTACAGCCTCAACCTCCCAGGCTCAAGTGATCCTCCCATCTTAGCCTCCCAAGTAGTT CAGCTCGTTACAGCCTCAACCTCCCAGGCTCAGGTGATCCTCCCATCTTAGCCTCCCAAGTAGTT T C DNAJC7 Ensembl:ENSG00000168259 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1262941634 Functional Loss SNV dbSNP153 33..33 33 - - - 50528 RMVar_ID_50528 Human_SNP_ID_624522790 A-to-I Human chr17 - 42006196 42006196 42006196 TGAGCCGAGATTGCGCCACTGCACTCCAGCCTAGGTAACAGAGGTGACAGAGGTCAGGAGATTGA TGAGCCGAGATTGCGCCACTGCACTCCAGCCTGGGTAACAGAGGTGACAGAGGTCAGGAGATTGA T C DNAJC7 Ensembl:ENSG00000168259 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1224495978 Functional Loss SNV dbSNP153 33..33 33 - - - 50529 RMVar_ID_50529 Human_SNP_ID_624523312 A-to-I Human chr17 - 42008147 42008147 42008147 CCATCATGCCCGGCTAATTTTTGTATTTTTGTAGAGATGGGGTTTCACCATGTTGCCTAGGCTGG CCATCATGCCCGGCTAATTTTTGTATTTTTGTGGAGATGGGGTTTCACCATGTTGCCTAGGCTGG T C DNAJC7 Ensembl:ENSG00000168259 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs761238696 Functional Loss SNV dbSNP153 33..33 33 - - - 50530 RMVar_ID_50530 Human_SNP_ID_624524962 A-to-I Human chr17 - 42015183 42015183 42015183 CTGAGGTCGGGAGTTTGAAACCAGCATGGCCAACATGGCAGAACCCTGTCTCTACTAAAAATACA CTGAGGTCGGGAGTTTGAAACCAGCATGGCCAGCATGGCAGAACCCTGTCTCTACTAAAAATACA T C DNAJC7 Ensembl:ENSG00000168259 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs993051330 Functional Loss SNV dbSNP153 33..33 33 - - - 50531 RMVar_ID_50531 Human_SNP_ID_624550940 A-to-I Human chr17 - 42117727 42117727 42117727 TGTGATGGGTGACATCCCCATGGAGCTGGTCAATGAGGTCATGCTGACCATCACTGACCCTGCTG TGTGATGGGTGACATCCCCATGGAGCTGGTCATTGAGGTCATGCTGACCATCACTGACCCTGCTG T A KAT2A Ensembl:ENSG00000108773 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs903845358 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_489521,Human_RBP_ID_8452470,Human_RBP_ID_8818021,Human_RBP_ID_18164722,Human_RBP_ID_18988450,Human_RBP_ID_22658808,Human_RBP_ID_22804475 Human_Splice_Rec_1818398,Human_Splice_Rec_1818399,Human_Splice_Rec_1818432,Human_Splice_Rec_1818433 Human_miRNA_ID_606486 RMVar_hsa_circ_184288,RMVar_hsa_circ_92003,RMVar_hsa_circ_104099,RMVar_hsa_circ_119819,RMVar_hsa_circ_111845,RMVar_hsa_circ_96780,RMVar_hsa_circ_89401,RMVar_hsa_circ_90640,RMVar_hsa_circ_81488,RMVar_hsa_circ_184292,RMVar_hsa_circ_184294,RMVar_hsa_circ_184293,RMVar_hsa_circ_184290,RMVar_hsa_circ_184291,RMVar_hsa_circ_184289,RMVar_hsa_circ_112231,RMVar_hsa_circ_184287,RMVar_hsa_circ_119273,RMVar_hsa_circ_184299,RMVar_hsa_circ_93964,RMVar_hsa_circ_184301,RMVar_hsa_circ_184306,RMVar_hsa_circ_127682,RMVar_hsa_circ_97657,RMVar_hsa_circ_184303,RMVar_hsa_circ_184304,RMVar_hsa_circ_184305 50532 RMVar_ID_50532 Human_SNP_ID_624550941 A-to-I Human chr17 - 42117727 42117727 42117727 TGTGATGGGTGACATCCCCATGGAGCTGGTCAATGAGGTCATGCTGACCATCACTGACCCTGCTG TGTGATGGGTGACATCCCCATGGAGCTGGTCAGTGAGGTCATGCTGACCATCACTGACCCTGCTG T C KAT2A Ensembl:ENSG00000108773 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs903845358 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_489521,Human_RBP_ID_8452470,Human_RBP_ID_8818021,Human_RBP_ID_18164722,Human_RBP_ID_18988450,Human_RBP_ID_22658808,Human_RBP_ID_22804475 Human_Splice_Rec_1818398,Human_Splice_Rec_1818399,Human_Splice_Rec_1818432,Human_Splice_Rec_1818433 Human_miRNA_ID_606486 RMVar_hsa_circ_184288,RMVar_hsa_circ_92003,RMVar_hsa_circ_104099,RMVar_hsa_circ_119819,RMVar_hsa_circ_111845,RMVar_hsa_circ_96780,RMVar_hsa_circ_89401,RMVar_hsa_circ_90640,RMVar_hsa_circ_81488,RMVar_hsa_circ_184292,RMVar_hsa_circ_184294,RMVar_hsa_circ_184293,RMVar_hsa_circ_184290,RMVar_hsa_circ_184291,RMVar_hsa_circ_184289,RMVar_hsa_circ_112231,RMVar_hsa_circ_184287,RMVar_hsa_circ_119273,RMVar_hsa_circ_184299,RMVar_hsa_circ_93964,RMVar_hsa_circ_184301,RMVar_hsa_circ_184306,RMVar_hsa_circ_127682,RMVar_hsa_circ_97657,RMVar_hsa_circ_184303,RMVar_hsa_circ_184304,RMVar_hsa_circ_184305 50533 RMVar_ID_50533 Human_SNP_ID_624552092 A-to-I Human chr17 - 42121110 42121110 42121110 GCCGGCAGCACAGGGACTGGGGGGCCCGGGGTAGGAAGTGGGGGGGCCGGGAGCGGGGGGGATCC GCCGGCAGCACAGGGACTGGGGGGCCCGGGGTGGGAAGTGGGGGGGCCGGGAGCGGGGGGGATCC T C AC099811.2,KAT2A Ensembl:ENSG00000267261,Ensembl:ENSG00000108773 Protein coding,Protein coding intron,CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1555667258 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9326631,Human_RBP_ID_22585990 RMVar_hsa_circ_111845,RMVar_hsa_circ_25379,RMVar_hsa_circ_184287 50534 RMVar_ID_50534 Human_SNP_ID_624574888 A-to-I Human chr17 - 42205833 42205833 42205833 GAGTACATTGCTCACTGCAGTCTCAAACTGCTAGACTCAAGGGATCCTCCCACCTCAGCCTCCCA GAGTACATTGCTCACTGCAGTCTCAAACTGCTGGACTCAAGGGATCCTCCCACCTCAGCCTCCCA T C STAT5B Ensembl:ENSG00000173757 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs745649448 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_184315,RMVar_hsa_circ_106124,RMVar_hsa_circ_265442 50535 RMVar_ID_50535 Human_SNP_ID_624574890 A-to-I Human chr17 - 42205840 42205840 42205840 CAGGCTGGAGTACATTGCTCACTGCAGTCTCAAACTGCTAGACTCAAGGGATCCTCCCACCTCAG CAGGCTGGAGTACATTGCTCACTGCAGTCTCAGACTGCTAGACTCAAGGGATCCTCCCACCTCAG T C STAT5B Ensembl:ENSG00000173757 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs940497154 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_184315,RMVar_hsa_circ_106124,RMVar_hsa_circ_265442 50536 RMVar_ID_50536 Human_SNP_ID_624575569 A-to-I Human chr17 - 42208378 42208378 42208378 CATTCTCCTACCTCAGCATAGTACCTGGGACTACGGATGAGTGCCACCACACTTGGCTGATTTTT CATTCTCCTACCTCAGCATAGTACCTGGGACTGCGGATGAGTGCCACCACACTTGGCTGATTTTT T C STAT5B Ensembl:ENSG00000173757 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs913705381 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_53270,RMVar_hsa_circ_184316,RMVar_hsa_circ_265442,RMVar_hsa_circ_71461,RMVar_hsa_circ_303239,RMVar_hsa_circ_317116,RMVar_hsa_circ_56325,RMVar_hsa_circ_184317 50537 RMVar_ID_50537 Human_SNP_ID_624575570 A-to-I Human chr17 - 42208378 42208378 42208378 CATTCTCCTACCTCAGCATAGTACCTGGGACTACGGATGAGTGCCACCACACTTGGCTGATTTTT CATTCTCCTACCTCAGCATAGTACCTGGGACTCCGGATGAGTGCCACCACACTTGGCTGATTTTT T G STAT5B Ensembl:ENSG00000173757 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs913705381 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_53270,RMVar_hsa_circ_184316,RMVar_hsa_circ_265442,RMVar_hsa_circ_71461,RMVar_hsa_circ_303239,RMVar_hsa_circ_317116,RMVar_hsa_circ_56325,RMVar_hsa_circ_184317 50538 RMVar_ID_50538 Human_SNP_ID_624575575 A-to-I Human chr17 - 42208401 42208401 42208401 ACCTCCACCTCCCAGCTTCAAGCCATTCTCCTACCTCAGCATAGTACCTGGGACTACGGATGAGT ACCTCCACCTCCCAGCTTCAAGCCATTCTCCTGCCTCAGCATAGTACCTGGGACTACGGATGAGT T C STAT5B Ensembl:ENSG00000173757 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs922549603 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_53270,RMVar_hsa_circ_184316,RMVar_hsa_circ_265442,RMVar_hsa_circ_71461,RMVar_hsa_circ_303239,RMVar_hsa_circ_317116,RMVar_hsa_circ_56325,RMVar_hsa_circ_184317 50539 RMVar_ID_50539 Human_SNP_ID_624580846 A-to-I Human chr17 - 42228769 42228769 42228769 CCGCCACGCCCGGATAATTTCTTTTGTGTTTTAGTAGAGATGGGGTTTCACCGTGTTGCCCAGGC CCGCCACGCCCGGATAATTTCTTTTGTGTTTTGGTAGAGATGGGGTTTCACCGTGTTGCCCAGGC T C STAT5B Ensembl:ENSG00000173757 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1014713515 Functional Loss SNV dbSNP153 33..33 33 - - - 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 50540 RMVar_ID_50540 Human_SNP_ID_624581083 A-to-I Human chr17 - 42229705 42229705 42229705 CACCACACCGAGCTAATTTTTGTATTTTTAATAGAGACGGGGTTTCATCATGTTGGCCAGGCTGG CACCACACCGAGCTAATTTTTGTATTTTTAATGGAGACGGGGTTTCATCATGTTGGCCAGGCTGG T C STAT5B Ensembl:ENSG00000173757 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1421299753 Functional Loss SNV dbSNP153 33..33 33 - - - 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 50541 RMVar_ID_50541 Human_SNP_ID_624584765 A-to-I Human chr17 - 42245492 42245492 42245492 AAAAATTAGCCAGGCATTGGTGGCAGATGCCTATGGTCCCAGCTGCTCAGGAGGCTGAGACAAGA AAAAATTAGCCAGGCATTGGTGGCAGATGCCTGTGGTCCCAGCTGCTCAGGAGGCTGAGACAAGA T C STAT5B Ensembl:ENSG00000173757 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1051272926 Functional Loss SNV dbSNP153 33..33 33 - - - 50542 RMVar_ID_50542 Human_SNP_ID_624585750 A-to-I Human chr17 - 42249760 42249760 42249760 GCTACTCAGGAGACTGAGACAAGAGGATTGCTAGAGCCTGGGAGGCAGAGGTTGCAGGGAGCTGA GCTACTCAGGAGACTGAGACAAGAGGATTGCTGGAGCCTGGGAGGCAGAGGTTGCAGGGAGCTGA T C STAT5B Ensembl:ENSG00000173757 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1189593958 Functional Loss SNV dbSNP153 33..33 33 - - - 50543 RMVar_ID_50543 Human_SNP_ID_624586643 A-to-I Human chr17 - 42253751 42253751 42253751 AGATGACTTGAGGCCAGGAGTCACAGGCTGCAATGAGTTGTGTTCATGCCACTGCTCTCCAGTCT AGATGACTTGAGGCCAGGAGTCACAGGCTGCAGTGAGTTGTGTTCATGCCACTGCTCTCCAGTCT T C STAT5B Ensembl:ENSG00000173757 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968586635 Functional Loss SNV dbSNP153 33..33 33 - - - 50544 RMVar_ID_50544 Human_SNP_ID_624588006 A-to-I Human chr17 - 42259700 42259700 42259700 TCACTGAAGCCTCCCCCCGACAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGA TCACTGAAGCCTCCCCCCGACAGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGA T C STAT5B Ensembl:ENSG00000173757 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1012686629 Functional Loss SNV dbSNP153 33..33 33 - - - 50545 RMVar_ID_50545 Human_SNP_ID_624590194 A-to-I Human chr17 - 42266627 42266627 42266627 CCTCCACACCTCCCACCTCAACCTTCCACAGTATTGGGATTACAGGAATGAGTCACTGCACCGGG CCTCCACACCTCCCACCTCAACCTTCCACAGTGTTGGGATTACAGGAATGAGTCACTGCACCGGG T C STAT5B Ensembl:ENSG00000173757 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1209741007 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8452549 50546 RMVar_ID_50546 Human_SNP_ID_624590762 A-to-I Human chr17 - 42269152 42269151 42269152 GAAGAATCACTTGAACCCAGGAGGCAGAGGTTACAGTGAGCCGAGATCGCACTACTGTGCTCCAG GAAGAATCACTTGAACCCAGGAGGCAGAGGTT_CAGTGAGCCGAGATCGCACTACTGTGCTCCAG GT G STAT5B Ensembl:ENSG00000173757 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1364515510 Functional Loss DEL dbSNP153 33..33 33 - - - 50547 RMVar_ID_50547 Human_SNP_ID_624591009 A-to-I Human chr17 - 42270203 42270203 42270203 TGGGCTAATTTATTATTATTATTTCTTGAGACAGAGCCTCGCTCTGTCACCCAGGCTGGAATGCA TGGGCTAATTTATTATTATTATTTCTTGAGACCGAGCCTCGCTCTGTCACCCAGGCTGGAATGCA T G STAT5B Ensembl:ENSG00000173757 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1489806711 Functional Loss SNV dbSNP153 33..33 33 - - - 50548 RMVar_ID_50548 Human_SNP_ID_624603190 A-to-I Human chr17 - 42318259 42318259 42318259 AAATTAGCTAGGCATGGTGGCAGATGCCTGTAATCCAGCTACTCAGGAGGCTGATGAAGGAGAAT AAATTAGCTAGGCATGGTGGCAGATGCCTGTAGTCCAGCTACTCAGGAGGCTGATGAAGGAGAAT T C STAT3 Ensembl:ENSG00000168610 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1053420950 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17565928 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 50549 RMVar_ID_50549 Human_SNP_ID_624603196 A-to-I Human chr17 - 42318278 42318278 42318278 TACTAAAATTACAAAAAAAAAATTAGCTAGGCATGGTGGCAGATGCCTGTAATCCAGCTACTCAG TACTAAAATTACAAAAAAAAAATTAGCTAGGCGTGGTGGCAGATGCCTGTAATCCAGCTACTCAG T C STAT3 Ensembl:ENSG00000168610 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs969649339 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17565928 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 50550 RMVar_ID_50550 Human_SNP_ID_624603434 A-to-I Human chr17 - 42319459 42319459 42319459 TGCTTCACTGAAACCTCTGCCTCCCAGGTTCAAGAGATTCTCATACCTCAGCCTCCTGAGTAGCT TGCTTCACTGAAACCTCTGCCTCCCAGGTTCAGGAGATTCTCATACCTCAGCCTCCTGAGTAGCT T C STAT3 Ensembl:ENSG00000168610 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1200407841 Functional Loss SNV dbSNP153 33..33 33 - - - 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 50551 RMVar_ID_50551 Human_SNP_ID_624604772 A-to-I Human chr17 - 42324841 42324841 42324841 AACAAGCAAATGTGTTCTTTCCAATAGAATGTAAACTTTTTTACCAAGCCCCCAATTGGAACCTG AACAAGCAAATGTGTTCTTTCCAATAGAATGTGAACTTTTTTACCAAGCCCCCAATTGGAACCTG T C STAT3 Ensembl:ENSG00000168610 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1141117 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1819064,Human_Splice_Rec_1819108,Human_Splice_Rec_1819150,Human_Splice_Rec_1819194,Human_Splice_Rec_1819240,Human_Splice_Rec_1819260,Human_Splice_Rec_1819264 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_184345,RMVar_hsa_circ_94403,RMVar_hsa_circ_127938,RMVar_hsa_circ_100328,RMVar_hsa_circ_76369,RMVar_hsa_circ_184347,RMVar_hsa_circ_184348,RMVar_hsa_circ_184346,RMVar_hsa_circ_56848,RMVar_hsa_circ_356342,RMVar_hsa_circ_374113,RMVar_hsa_circ_319575,RMVar_hsa_circ_184350,RMVar_hsa_circ_40575,RMVar_hsa_circ_267623,RMVar_hsa_circ_284199,RMVar_hsa_circ_348724,RMVar_hsa_circ_378740,RMVar_hsa_circ_184351 50552 RMVar_ID_50552 Human_SNP_ID_624606591 A-to-I Human chr17 - 42331966 42331966 42331966 CGGAGATTGCGCCATTGCACTCCAGCCTGGGTAACGAGAGAAACTGTCTCAAAAAAAAAAAAAGA CGGAGATTGCGCCATTGCACTCCAGCCTGGGTGACGAGAGAAACTGTCTCAAAAAAAAAAAAAGA T C STAT3 Ensembl:ENSG00000168610 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs867167168 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12314,RMVar_hsa_circ_104685,RMVar_hsa_circ_184342,RMVar_hsa_circ_94403,RMVar_hsa_circ_184348,RMVar_hsa_circ_36903,RMVar_hsa_circ_356342,RMVar_hsa_circ_40575,RMVar_hsa_circ_62294,RMVar_hsa_circ_18776,RMVar_hsa_circ_58313,RMVar_hsa_circ_358497,RMVar_hsa_circ_52152,RMVar_hsa_circ_356236,RMVar_hsa_circ_312995,RMVar_hsa_circ_346026,RMVar_hsa_circ_62431,RMVar_hsa_circ_50548 50553 RMVar_ID_50553 Human_SNP_ID_624607663 A-to-I Human chr17 - 42336476 42336476 42336476 TTCCCACCTTAGCCTTCTCAGTAGCTGGGACTACAGGCATGCACCACCACACCTGGCTAATTTTT TTCCCACCTTAGCCTTCTCAGTAGCTGGGACTGCAGGCATGCACCACCACACCTGGCTAATTTTT T C STAT3 Ensembl:ENSG00000168610 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1324553599 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12314,RMVar_hsa_circ_104685,RMVar_hsa_circ_184342,RMVar_hsa_circ_17988,RMVar_hsa_circ_94403,RMVar_hsa_circ_184348,RMVar_hsa_circ_36903,RMVar_hsa_circ_356342,RMVar_hsa_circ_40575,RMVar_hsa_circ_62294,RMVar_hsa_circ_18776,RMVar_hsa_circ_58313,RMVar_hsa_circ_358497,RMVar_hsa_circ_52152,RMVar_hsa_circ_356236,RMVar_hsa_circ_312995,RMVar_hsa_circ_346026,RMVar_hsa_circ_61291,RMVar_hsa_circ_364172,RMVar_hsa_circ_50548,RMVar_hsa_circ_26602,RMVar_hsa_circ_71135 50554 RMVar_ID_50554 Human_SNP_ID_624611116 A-to-I Human chr17 - 42351435 42351435 42351435 GTCTAGGAGTTTGAGACCAGCCTGGGCAACACAGTAGGACCCCGTCTCTACAAAAATAATCAGCC GTCTAGGAGTTTGAGACCAGCCTGGGCAACACTGTAGGACCCCGTCTCTACAAAAATAATCAGCC T A STAT3 Ensembl:ENSG00000168610 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1017323050 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94403,RMVar_hsa_circ_184348,RMVar_hsa_circ_184361,RMVar_hsa_circ_111092 50555 RMVar_ID_50555 Human_SNP_ID_624611133 A-to-I Human chr17 - 42351502 42351502 42351502 TTTTTGTGGGCTGGACACGGTGGCTCAAGCCTATACTCTTGGCACATTGGGAGGCTGAGATGCAT TTTTTGTGGGCTGGACACGGTGGCTCAAGCCTGTACTCTTGGCACATTGGGAGGCTGAGATGCAT T C STAT3 Ensembl:ENSG00000168610 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017984494 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13007326 RMVar_hsa_circ_94403,RMVar_hsa_circ_184348,RMVar_hsa_circ_184361,RMVar_hsa_circ_111092 50556 RMVar_ID_50556 Human_SNP_ID_624612591 A-to-I Human chr17 - 42357489 42357489 42357489 TTTTGTATTTTTAGTAGAGACAGGCTTTTGCCATGTTAGCCTGGCTGGTCTCGAACTCCTGACCT TTTTGTATTTTTAGTAGAGACAGGCTTTTGCCGTGTTAGCCTGGCTGGTCTCGAACTCCTGACCT T C STAT3 Ensembl:ENSG00000168610 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1226472130 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94403,RMVar_hsa_circ_184348,RMVar_hsa_circ_184361,RMVar_hsa_circ_111092 50557 RMVar_ID_50557 Human_SNP_ID_624615966 A-to-I Human chr17 - 42371725 42371725 42371725 CACCTGCCTCAGCTTCCCAAAGTGTTAGGATTACAGGCATGAGCCACCGCACCTGGCCTCAATTT CACCTGCCTCAGCTTCCCAAAGTGTTAGGATTGCAGGCATGAGCCACCGCACCTGGCCTCAATTT T C STAT3 Ensembl:ENSG00000168610 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs955384463 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94403,RMVar_hsa_circ_184348,RMVar_hsa_circ_184361,RMVar_hsa_circ_111092 50558 RMVar_ID_50558 Human_SNP_ID_624618052 A-to-I Human chr17 - 42380830 42380830 42380830 CAGCTCATGACAGCCTTGACCTCCTAGGCTCAAGTGATCCTCCTGCCTCAGCCTTCGGGGTAGCT CAGCTCATGACAGCCTTGACCTCCTAGGCTCAGGTGATCCTCCTGCCTCAGCCTTCGGGGTAGCT T C STAT3 Ensembl:ENSG00000168610 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs932327106 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94403,RMVar_hsa_circ_184348,RMVar_hsa_circ_184361,RMVar_hsa_circ_111092 50559 RMVar_ID_50559 Human_SNP_ID_624619495 A-to-I Human chr17 - 42386691 42386691 42386691 AAGAATAATCACTTAGAAATATCCACAGTGCCAGGCATGGTGGTGCACACCTCTGATCCCAGCTA AAGAATAATCACTTAGAAATATCCACAGTGCCGGGCATGGTGGTGCACACCTCTGATCCCAGCTA T C STAT3 Ensembl:ENSG00000168610 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900037227 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2529578 RMVar_hsa_circ_94403,RMVar_hsa_circ_184348,RMVar_hsa_circ_184361,RMVar_hsa_circ_111092 50560 RMVar_ID_50560 Human_SNP_ID_624626672 A-to-I Human chr17 - 42413528 42413528 42413528 TTGAGACAGACTTTTGCTCTGTCGCCCAGGCTAGAGTGAAGTGGCTGGACCTCAGCTCACTGCAA TTGAGACAGACTTTTGCTCTGTCGCCCAGGCTGGAGTGAAGTGGCTGGACCTCAGCTCACTGCAA T C CAVIN1 Ensembl:ENSG00000177469 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs889857511 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2506808 RMVar_hsa_circ_112675,RMVar_hsa_circ_116285,RMVar_hsa_circ_184363,RMVar_hsa_circ_94674,RMVar_hsa_circ_184364,RMVar_hsa_circ_184362 50561 RMVar_ID_50561 Human_SNP_ID_624628058 A-to-I Human chr17 - 42419085 42419085 42419085 TCAAGTGATCCTCCTGGTTCAGCCTCCCGAGTAGCTAGGACTACAGGTGCCCACCACCGTGCCCG TCAAGTGATCCTCCTGGTTCAGCCTCCCGAGTGGCTAGGACTACAGGTGCCCACCACCGTGCCCG T C CAVIN1 Ensembl:ENSG00000177469 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1270811070 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112675,RMVar_hsa_circ_116285,RMVar_hsa_circ_184363,RMVar_hsa_circ_94674,RMVar_hsa_circ_184364,RMVar_hsa_circ_184362 50562 RMVar_ID_50562 Human_SNP_ID_624628161 A-to-I Human chr17 - 42419450 42419450 42419450 AAATTAGCCGGGCATGGTGGTGAGCACCTCTAATCCTGGTTACTCGGGAGGCTGAGGCAGAAGAA AAATTAGCCGGGCATGGTGGTGAGCACCTCTAGTCCTGGTTACTCGGGAGGCTGAGGCAGAAGAA T C CAVIN1 Ensembl:ENSG00000177469 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170533762 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_112675,RMVar_hsa_circ_116285,RMVar_hsa_circ_184363,RMVar_hsa_circ_94674,RMVar_hsa_circ_184364,RMVar_hsa_circ_184362 50563 RMVar_ID_50563 Human_SNP_ID_624630066 A-to-I Human chr17 + 42426641 42426641 42426641 TATAACTGCTAGAACTGGCAGATTACCAACTTACTTTAGAATTTAGGAGAAATGTATTAAAGTAA TATAACTGCTAGAACTGGCAGATTACCAACTTCCTTTAGAATTTAGGAGAAATGTATTAAAGTAA A C lnc-ATP6V0A1-4,lnc-ATP6V0A1-4:2,lnc-ATP6V0A1-4:3 RNACentral:URS0000D5C72B,RNACentral:URS0000D59931,RNACentral:URS0000D5B9F9 lincRNA,lincRNA,lincRNA intron,intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1014514389 Functional Loss SNV dbSNP153 33..33 33 - - - 50564 RMVar_ID_50564 Human_SNP_ID_624641627 A-to-I Human chr17 + 42470913 42470912 42470914 GGGAGGCCGAGGCAGGTGGATCACCTGAGGTCAGGAGTTCGAGATCAGCCTGGCCAACATGGTGA GGGAGGCCGAGGCAGGTGGATCACCTGAGGTC__GAGTTCGAGATCAGCCTGGCCAACATGGTGA CAG C ATP6V0A1 Ensembl:ENSG00000033627 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1388216265 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_85058,RMVar_hsa_circ_100787,RMVar_hsa_circ_184366,RMVar_hsa_circ_373163,RMVar_hsa_circ_184369,RMVar_hsa_circ_184370,RMVar_hsa_circ_281366,RMVar_hsa_circ_314155,RMVar_hsa_circ_184372,RMVar_hsa_circ_184373 50565 RMVar_ID_50565 Human_SNP_ID_624641647 A-to-I Human chr17 + 42470958 42470958 42470958 CAGCCTGGCCAACATGGTGAAACCCGGTCTCTACTAAAAATACAAAAACTAGCCGGGTGAGGTGG CAGCCTGGCCAACATGGTGAAACCCGGTCTCTGCTAAAAATACAAAAACTAGCCGGGTGAGGTGG A G ATP6V0A1 Ensembl:ENSG00000033627 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1259854328 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85058,RMVar_hsa_circ_100787,RMVar_hsa_circ_184366,RMVar_hsa_circ_373163,RMVar_hsa_circ_184369,RMVar_hsa_circ_184370,RMVar_hsa_circ_281366,RMVar_hsa_circ_314155,RMVar_hsa_circ_184372,RMVar_hsa_circ_184373 50566 RMVar_ID_50566 Human_SNP_ID_624641650 A-to-I Human chr17 + 42470961 42470961 42470961 CCTGGCCAACATGGTGAAACCCGGTCTCTACTAAAAATACAAAAACTAGCCGGGTGAGGTGGTGG CCTGGCCAACATGGTGAAACCCGGTCTCTACTGAAAATACAAAAACTAGCCGGGTGAGGTGGTGG A G ATP6V0A1 Ensembl:ENSG00000033627 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1483745923 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85058,RMVar_hsa_circ_100787,RMVar_hsa_circ_184366,RMVar_hsa_circ_373163,RMVar_hsa_circ_184369,RMVar_hsa_circ_184370,RMVar_hsa_circ_281366,RMVar_hsa_circ_314155,RMVar_hsa_circ_184372,RMVar_hsa_circ_184373 50567 RMVar_ID_50567 Human_SNP_ID_624641734 A-to-I Human chr17 + 42471217 42471217 42471217 CCGAGGTGGGCGGATCACGAGGTCAGGAGATCAAGACCATCTTGGCTAACACGGTGAAACCCCGT CCGAGGTGGGCGGATCACGAGGTCAGGAGATCGAGACCATCTTGGCTAACACGGTGAAACCCCGT A G ATP6V0A1 Ensembl:ENSG00000033627 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1018352242 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85058,RMVar_hsa_circ_100787,RMVar_hsa_circ_184366,RMVar_hsa_circ_373163,RMVar_hsa_circ_184369,RMVar_hsa_circ_184370,RMVar_hsa_circ_281366,RMVar_hsa_circ_314155,RMVar_hsa_circ_184372,RMVar_hsa_circ_184373 50568 RMVar_ID_50568 Human_SNP_ID_624641767 A-to-I Human chr17 + 42471311 42471311 42471311 GGGCATGGTGGTGGGCACCTGTAGTCCCAGCTAATCAGGAGGCTGAGGCAGGAGAATGGCGTGAA GGGCATGGTGGTGGGCACCTGTAGTCCCAGCTCATCAGGAGGCTGAGGCAGGAGAATGGCGTGAA A C ATP6V0A1 Ensembl:ENSG00000033627 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1272079253 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85058,RMVar_hsa_circ_100787,RMVar_hsa_circ_184366,RMVar_hsa_circ_373163,RMVar_hsa_circ_184369,RMVar_hsa_circ_184370,RMVar_hsa_circ_281366,RMVar_hsa_circ_314155,RMVar_hsa_circ_184372,RMVar_hsa_circ_184373 50569 RMVar_ID_50569 Human_SNP_ID_624641864 A-to-I Human chr17 + 42471613 42471613 42471613 AAAATTAGACAGGCATCGTGGTGCACACCTGTAGTTCCAGCTACTCGGGAGGCTGAAGTGAGGGG AAAATTAGACAGGCATCGTGGTGCACACCTGTGGTTCCAGCTACTCGGGAGGCTGAAGTGAGGGG A G ATP6V0A1 Ensembl:ENSG00000033627 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1252542208 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85058,RMVar_hsa_circ_100787,RMVar_hsa_circ_184366,RMVar_hsa_circ_373163,RMVar_hsa_circ_184369,RMVar_hsa_circ_184370,RMVar_hsa_circ_281366,RMVar_hsa_circ_314155,RMVar_hsa_circ_184372,RMVar_hsa_circ_184373 50570 RMVar_ID_50570 Human_SNP_ID_624642446 A-to-I Human chr17 + 42474204 42474204 42474204 TTTGTAGTTTTAGTAGAGACGGGCGTTTCACCATATTGGCCAGGCTGGTCTCGAACTCTGACCTC TTTGTAGTTTTAGTAGAGACGGGCGTTTCACCGTATTGGCCAGGCTGGTCTCGAACTCTGACCTC A G ATP6V0A1 Ensembl:ENSG00000033627 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs980293338 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13007893 RMVar_hsa_circ_85058,RMVar_hsa_circ_100787,RMVar_hsa_circ_184366,RMVar_hsa_circ_373163,RMVar_hsa_circ_184369,RMVar_hsa_circ_184370,RMVar_hsa_circ_281366,RMVar_hsa_circ_314155,RMVar_hsa_circ_184372,RMVar_hsa_circ_184373 50571 RMVar_ID_50571 Human_SNP_ID_624642447 A-to-I Human chr17 + 42474206 42474206 42474206 TGTAGTTTTAGTAGAGACGGGCGTTTCACCATATTGGCCAGGCTGGTCTCGAACTCTGACCTCGT TGTAGTTTTAGTAGAGACGGGCGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCTGACCTCGT A G ATP6V0A1 Ensembl:ENSG00000033627 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1269272844 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13007893 RMVar_hsa_circ_85058,RMVar_hsa_circ_100787,RMVar_hsa_circ_184366,RMVar_hsa_circ_373163,RMVar_hsa_circ_184369,RMVar_hsa_circ_184370,RMVar_hsa_circ_281366,RMVar_hsa_circ_314155,RMVar_hsa_circ_184372,RMVar_hsa_circ_184373 50572 RMVar_ID_50572 Human_SNP_ID_624642461 A-to-I Human chr17 + 42474244 42474244 42474244 CAGGCTGGTCTCGAACTCTGACCTCGTGATCTAGCTGCCTCAGCCTCCCAAAGTGCTGGAATTAC CAGGCTGGTCTCGAACTCTGACCTCGTGATCTGGCTGCCTCAGCCTCCCAAAGTGCTGGAATTAC A G ATP6V0A1 Ensembl:ENSG00000033627 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs891146926 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13007893 RMVar_hsa_circ_85058,RMVar_hsa_circ_100787,RMVar_hsa_circ_184366,RMVar_hsa_circ_373163,RMVar_hsa_circ_184369,RMVar_hsa_circ_184370,RMVar_hsa_circ_281366,RMVar_hsa_circ_314155,RMVar_hsa_circ_184372,RMVar_hsa_circ_184373 50573 RMVar_ID_50573 Human_SNP_ID_624645765 A-to-I Human chr17 + 42488584 42488584 42488584 GCTTCCAACTCCTGGGCTTAAGCAATCCTCCCACTTCAGACTCCCGGTAGCTGGGACTACAGGTG GCTTCCAACTCCTGGGCTTAAGCAATCCTCCCTCTTCAGACTCCCGGTAGCTGGGACTACAGGTG A T ATP6V0A1 Ensembl:ENSG00000033627 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs955273742 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85058,RMVar_hsa_circ_100787,RMVar_hsa_circ_184366,RMVar_hsa_circ_373163,RMVar_hsa_circ_184369,RMVar_hsa_circ_184370,RMVar_hsa_circ_292335,RMVar_hsa_circ_97521,RMVar_hsa_circ_351445,RMVar_hsa_circ_297722,RMVar_hsa_circ_184376,RMVar_hsa_circ_184374,RMVar_hsa_circ_184375,RMVar_hsa_circ_309637,RMVar_hsa_circ_349356,RMVar_hsa_circ_344564,RMVar_hsa_circ_357524,RMVar_hsa_circ_307720,RMVar_hsa_circ_184380,RMVar_hsa_circ_271410,RMVar_hsa_circ_281137,RMVar_hsa_circ_354743,RMVar_hsa_circ_184378,RMVar_hsa_circ_184379,RMVar_hsa_circ_184377,RMVar_hsa_circ_369533,RMVar_hsa_circ_302426,RMVar_hsa_circ_334554,RMVar_hsa_circ_290468,RMVar_hsa_circ_51666,RMVar_hsa_circ_292206,RMVar_hsa_circ_184382,RMVar_hsa_circ_184383,RMVar_hsa_circ_184384,RMVar_hsa_circ_302328,RMVar_hsa_circ_345093,RMVar_hsa_circ_274434,RMVar_hsa_circ_274630,RMVar_hsa_circ_83294,RMVar_hsa_circ_184385,RMVar_hsa_circ_184387,RMVar_hsa_circ_184388,RMVar_hsa_circ_184389,RMVar_hsa_circ_184386 50574 RMVar_ID_50574 Human_SNP_ID_624649126 A-to-I Human chr17 + 42501508 42501508 42501508 ACGATCTTGGCTCACTGCAACCTCCACCTCCCAGGTTCAAGCAATTCTTTTGCCTCAGCCTCCTG ACGATCTTGGCTCACTGCAACCTCCACCTCCCGGGTTCAAGCAATTCTTTTGCCTCAGCCTCCTG A G ATP6V0A1 Ensembl:ENSG00000033627 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1400734032 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85058,RMVar_hsa_circ_184366,RMVar_hsa_circ_97521,RMVar_hsa_circ_351445,RMVar_hsa_circ_184376,RMVar_hsa_circ_184375,RMVar_hsa_circ_357524,RMVar_hsa_circ_51666,RMVar_hsa_circ_83294,RMVar_hsa_circ_184389,RMVar_hsa_circ_94499,RMVar_hsa_circ_184391,RMVar_hsa_circ_107670,RMVar_hsa_circ_127747,RMVar_hsa_circ_184394,RMVar_hsa_circ_184397 50575 RMVar_ID_50575 Human_SNP_ID_624649129 A-to-I Human chr17 + 42501518 42501518 42501518 CTCACTGCAACCTCCACCTCCCAGGTTCAAGCAATTCTTTTGCCTCAGCCTCCTGTGTCACTGGG CTCACTGCAACCTCCACCTCCCAGGTTCAAGCGATTCTTTTGCCTCAGCCTCCTGTGTCACTGGG A G ATP6V0A1 Ensembl:ENSG00000033627 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1343042557 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85058,RMVar_hsa_circ_184366,RMVar_hsa_circ_97521,RMVar_hsa_circ_351445,RMVar_hsa_circ_184376,RMVar_hsa_circ_184375,RMVar_hsa_circ_357524,RMVar_hsa_circ_51666,RMVar_hsa_circ_83294,RMVar_hsa_circ_184389,RMVar_hsa_circ_94499,RMVar_hsa_circ_184391,RMVar_hsa_circ_107670,RMVar_hsa_circ_127747,RMVar_hsa_circ_184394,RMVar_hsa_circ_184397 50576 RMVar_ID_50576 Human_SNP_ID_624658980 A-to-I Human chr17 + 42539993 42539993 42539993 AAAATTAGCCAGGCGTGGTGGCGGGCTCCTGTAATCCCAGCTACTCGGTAGGCTGAGGCATGAGA AAAATTAGCCAGGCGTGGTGGCGGGCTCCTGTGATCCCAGCTACTCGGTAGGCTGAGGCATGAGA A G AC067852.1,NAGLU Ensembl:ENSG00000266929,Ensembl:ENSG00000108784 lincRNA,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1252488078 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_184401,RMVar_hsa_circ_184399,RMVar_hsa_circ_117429,RMVar_hsa_circ_273151,RMVar_hsa_circ_113956,RMVar_hsa_circ_184402 50577 RMVar_ID_50577 Human_SNP_ID_624659665 A-to-I Human chr17 + 42542398 42542398 42542398 TTTTTGTATTTTTAGTAGAAACAGGTTTCACCATGGTGGCCAGACTGGTCTCAAACTCCTGACCT TTTTTGTATTTTTAGTAGAAACAGGTTTCACCGTGGTGGCCAGACTGGTCTCAAACTCCTGACCT A G AC067852.1,NAGLU Ensembl:ENSG00000266929,Ensembl:ENSG00000108784 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs964699797 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_184399,RMVar_hsa_circ_117429,RMVar_hsa_circ_113956,RMVar_hsa_circ_184402,RMVar_hsa_circ_82473,RMVar_hsa_circ_184403 50578 RMVar_ID_50578 Human_SNP_ID_624659703 A-to-I Human chr17 + 42542563 42542563 42542563 TCGCCCAGACTGGAGTGCAGTGGCACAATCTCAGCTCACTGCAACTTCTGCCTCATGGGTTCAAG TCGCCCAGACTGGAGTGCAGTGGCACAATCTCGGCTCACTGCAACTTCTGCCTCATGGGTTCAAG A G AC067852.1,NAGLU Ensembl:ENSG00000266929,Ensembl:ENSG00000108784 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1199998325 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_184399,RMVar_hsa_circ_117429,RMVar_hsa_circ_113956,RMVar_hsa_circ_184402,RMVar_hsa_circ_82473,RMVar_hsa_circ_184403 50579 RMVar_ID_50579 Human_SNP_ID_624662530 A-to-I Human chr17 - 42551916 42551915 42551917 GAGCCCAGGAGTTCAAGACCAGGCCAGGTAACAGAGTGAGACCCGGTCTCTGCAAAAAATATTAA GAGCCCAGGAGTTCAAGACCAGGCCAGGTAA__GAGTGAGACCCGGTCTCTGCAAAAAATATTAA CTG C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1181274739 Functional Loss DEL dbSNP153 32..33 33 - - - 50580 RMVar_ID_50580 Human_SNP_ID_624674107 A-to-I Human chr17 - 42588937 42588937 42588937 AGAGAACAGGCAGGCTGGGTGTGGTGGCTCACACCTGTAATTCCAGCACTTTAGGGAGGCTATGG AGAGAACAGGCAGGCTGGGTGTGGTGGCTCACCCCTGTAATTCCAGCACTTTAGGGAGGCTATGG T G RETREG3 Ensembl:ENSG00000141699 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1033403728 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5154,RMVar_hsa_circ_89113,RMVar_hsa_circ_184415,RMVar_hsa_circ_107844,RMVar_hsa_circ_184417,RMVar_hsa_circ_184418,RMVar_hsa_circ_376118 50581 RMVar_ID_50581 Human_SNP_ID_624674359 A-to-I Human chr17 - 42590035 42590035 42590035 TACGCCCAGCTAATTTTTTTGGTATTTTTAGTAGAAATGGGGTTTCGCCATGTTGGCCAGGCTGG TACGCCCAGCTAATTTTTTTGGTATTTTTAGTGGAAATGGGGTTTCGCCATGTTGGCCAGGCTGG T C RETREG3 Ensembl:ENSG00000141699 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs900907705 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5154,RMVar_hsa_circ_89113,RMVar_hsa_circ_184415,RMVar_hsa_circ_107844,RMVar_hsa_circ_184417,RMVar_hsa_circ_184418,RMVar_hsa_circ_376118 50582 RMVar_ID_50582 Human_SNP_ID_624676256 A-to-I Human chr17 - 42596965 42596965 42596965 GGGAGACTAGGACAGGAGAATTGCTTGAACCCAGGAGGCAGAGGTTGCAGTGAGCCAAGATGGCG GGGAGACTAGGACAGGAGAATTGCTTGAACCCGGGAGGCAGAGGTTGCAGTGAGCCAAGATGGCG T C RETREG3 Ensembl:ENSG00000141699 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1410493561 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26758806 RMVar_hsa_circ_107844,RMVar_hsa_circ_184417 50583 RMVar_ID_50583 Human_SNP_ID_624676926 A-to-I Human chr17 - 42598262 42598262 42598262 ACTTCAGAGGAAGAGGCCGGGTGCGGTGGCTCACGTCTGTAATCCCAGCACTTTGGGAGGCTGAG ACTTCAGAGGAAGAGGCCGGGTGCGGTGGCTCCCGTCTGTAATCCCAGCACTTTGGGAGGCTGAG T G RETREG3 Ensembl:ENSG00000141699 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903927507 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107844,RMVar_hsa_circ_184417 50584 RMVar_ID_50584 Human_SNP_ID_624677179 A-to-I Human chr17 - 42599467 42599467 42599467 TATTTTTAATAGACATGGAGTTTCTCCATGTTAGCTAGGCTGGTCTCAAACTCCCGATCTCAGGT TATTTTTAATAGACATGGAGTTTCTCCATGTTTGCTAGGCTGGTCTCAAACTCCCGATCTCAGGT T A RETREG3 Ensembl:ENSG00000141699 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs572476066 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107844,RMVar_hsa_circ_184417 50585 RMVar_ID_50585 Human_SNP_ID_624677620 A-to-I Human chr17 - 42601338 42601338 42601338 TCGATCTCCTGATCTCGTGATCTGCCTGCCTCAGCCTCCCAAAGTGTTGGGATTACAGGCTTGAG TCGATCTCCTGATCTCGTGATCTGCCTGCCTCTGCCTCCCAAAGTGTTGGGATTACAGGCTTGAG T A RETREG3 Ensembl:ENSG00000141699 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1304682458 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107844,RMVar_hsa_circ_184417 50586 RMVar_ID_50586 Human_SNP_ID_624677854 A-to-I Human chr17 - 42602090 42602090 42602090 AGTGGTCTTGAACTCTTGACCTCAAGTGACCCACCTGCCTCGGCCTCCCAAAGGCTGGGATTACA AGTGGTCTTGAACTCTTGACCTCAAGTGACCCGCCTGCCTCGGCCTCCCAAAGGCTGGGATTACA T C RETREG3 Ensembl:ENSG00000141699 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1419252491 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25284709 RMVar_hsa_circ_107844,RMVar_hsa_circ_184417 50587 RMVar_ID_50587 Human_SNP_ID_624677874 A-to-I Human chr17 - 42602195 42602195 42602195 CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACCGGCGTGCACCACCATGTCTTGGCTGATTTT CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTGCCGGCGTGCACCACCATGTCTTGGCTGATTTT T C RETREG3 Ensembl:ENSG00000141699 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs774176958 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107844,RMVar_hsa_circ_184417 50588 RMVar_ID_50588 Human_SNP_ID_624678435 A-to-I Human chr17 - 42604489 42604489 42604489 ATTTGCAAAACTTTTGTAGAGACAGAATCTCAATATGTTGCCCAGGCTGGTCTCAAACTCCTCAT ATTTGCAAAACTTTTGTAGAGACAGAATCTCAGTATGTTGCCCAGGCTGGTCTCAAACTCCTCAT T C RETREG3 Ensembl:ENSG00000141699 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1159440441 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_107844,RMVar_hsa_circ_184417 50589 RMVar_ID_50589 Human_SNP_ID_624691347 A-to-I Human chr17 - 42655126 42655126 42655126 GCCAGGTGTGGTTGGTGGGTGTCTGTAATCCCAGCTACAAGGGAGGCTAAGGCAATGAGAATCGC GCCAGGTGTGGTTGGTGGGTGTCTGTAATCCCGGCTACAAGGGAGGCTAAGGCAATGAGAATCGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1402252413 Functional Loss SNV dbSNP153 33..33 33 - - - 50590 RMVar_ID_50590 Human_SNP_ID_624691348 A-to-I Human chr17 - 42655126 42655126 42655126 GCCAGGTGTGGTTGGTGGGTGTCTGTAATCCCAGCTACAAGGGAGGCTAAGGCAATGAGAATCGC GCCAGGTGTGGTTGGTGGGTGTCTGTAATCCCCGCTACAAGGGAGGCTAAGGCAATGAGAATCGC T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1402252413 Functional Loss SNV dbSNP153 33..33 33 - - - 50591 RMVar_ID_50591 Human_SNP_ID_624711293 A-to-I Human chr17 - 42728393 42728393 42728393 AAATCGTAACAGGGCCAGGTGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTAAGGC AAATCGTAACAGGGCCAGGTGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTAAGGC T C EZH1 Ensembl:ENSG00000108799 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1275929131 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_325671,RMVar_hsa_circ_282874,RMVar_hsa_circ_610,RMVar_hsa_circ_184466,RMVar_hsa_circ_365604,RMVar_hsa_circ_50467,RMVar_hsa_circ_53896,RMVar_hsa_circ_42528,RMVar_hsa_circ_365340,RMVar_hsa_circ_369046,RMVar_hsa_circ_53805,RMVar_hsa_circ_115949,RMVar_hsa_circ_184478,RMVar_hsa_circ_71269,RMVar_hsa_circ_184482,RMVar_hsa_circ_184479,RMVar_hsa_circ_184480,RMVar_hsa_circ_272102,RMVar_hsa_circ_310022,RMVar_hsa_circ_184483,RMVar_hsa_circ_184484,RMVar_hsa_circ_286188,RMVar_hsa_circ_316528 50592 RMVar_ID_50592 Human_SNP_ID_624713914 A-to-I Human chr17 - 42738870 42738869 42738870 ATAGTCCCAGCTACTCAGGGGGGGTGGAGGCAAGAGAATCGCTTGAACCCAGGAGGTGGAGATTG ATAGTCCCAGCTACTCAGGGGGGGTGGAGGCA_GAGAATCGCTTGAACCCAGGAGGTGGAGATTG CT C EZH1 Ensembl:ENSG00000108799 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1180472357 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_115949,RMVar_hsa_circ_184480 50593 RMVar_ID_50593 Human_SNP_ID_624717810 A-to-I Human chr17 - 42755738 42755738 42755738 CGAGACCAGCCAGAACAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTTGCTGGGCG CGAGACCAGCCAGAACAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTTGCTGGGCG T C RAMP2-AS1 Ensembl:ENSG00000197291 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1180097908 Functional Loss SNV dbSNP153 33..33 33 - - - 50594 RMVar_ID_50594 Human_SNP_ID_624723365 A-to-I Human chr17 + 42777566 42777566 42777566 ATAAAAAAAATTATAAATAACTTTCTTCATTCAGCATCTGCTATAGATGCCGAATGAGAAACAAG ATAAAAAAAATTATAAATAACTTTCTTCATTCCGCATCTGCTATAGATGCCGAATGAGAAACAAG A C VPS25 Ensembl:ENSG00000131475 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1341356949 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_110739,RMVar_hsa_circ_107108,RMVar_hsa_circ_184490,RMVar_hsa_circ_88765,RMVar_hsa_circ_184491,RMVar_hsa_circ_124241,RMVar_hsa_circ_184494,RMVar_hsa_circ_102950,RMVar_hsa_circ_184495,RMVar_hsa_circ_184496 50595 RMVar_ID_50595 Human_SNP_ID_624732980 A-to-I Human chr17 - 42812128 42812128 42812128 TGCCCACCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCTCCTGGTCTATTTAT TGCCCACCTTGGCCTCCCAAAGTGCTGGGATTGCAGGCGTGAGCCACTGCTCCTGGTCTATTTAT T C BECN1 Ensembl:ENSG00000126581 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs111276528 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79658,RMVar_hsa_circ_184501 50596 RMVar_ID_50596 Human_SNP_ID_624732983 A-to-I Human chr17 - 42812141 42812141 42812141 ACCTCAGGTGATCTGCCCACCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCTC ACCTCAGGTGATCTGCCCACCTTGGCCTCCCAGAGTGCTGGGATTACAGGCGTGAGCCACTGCTC T C BECN1 Ensembl:ENSG00000126581 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1489238793 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79658,RMVar_hsa_circ_184501 50597 RMVar_ID_50597 Human_SNP_ID_624732996 A-to-I Human chr17 - 42812173 42812173 42812173 TCCATGTTGGTCAGGCTAGTCTCAAACTCCCAACCTCAGGTGATCTGCCCACCTTGGCCTCCCAA TCCATGTTGGTCAGGCTAGTCTCAAACTCCCAGCCTCAGGTGATCTGCCCACCTTGGCCTCCCAA T C BECN1 Ensembl:ENSG00000126581 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1567667750 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79658,RMVar_hsa_circ_184501 50598 RMVar_ID_50598 Human_SNP_ID_624732998 A-to-I Human chr17 - 42812181 42812176 42812182 GGGGTTTCTCCATGTTGGTCAGGCTAGTCTCAAACTCCCAACCTCAGGTGATCTGCCCACCTTGG GGGGTTTCTCCATGTTGGTCAGGCTAGTCTC______CCAACCTCAGGTGATCTGCCCACCTTGG GGAGTTT G BECN1 Ensembl:ENSG00000126581 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1388848116 Functional Loss DEL dbSNP153 32..37 33 - - - RMVar_hsa_circ_79658,RMVar_hsa_circ_184501 50599 RMVar_ID_50599 Human_SNP_ID_624733000 A-to-I Human chr17 - 42812188 42812188 42812188 TAGAGACGGGGTTTCTCCATGTTGGTCAGGCTAGTCTCAAACTCCCAACCTCAGGTGATCTGCCC TAGAGACGGGGTTTCTCCATGTTGGTCAGGCTGGTCTCAAACTCCCAACCTCAGGTGATCTGCCC T C BECN1 Ensembl:ENSG00000126581 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1423699772 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79658,RMVar_hsa_circ_184501 50600 RMVar_ID_50600 Human_SNP_ID_624733003 A-to-I Human chr17 - 42812202 42812202 42812202 TTAGGTATTTTTAGTAGAGACGGGGTTTCTCCATGTTGGTCAGGCTAGTCTCAAACTCCCAACCT TTAGGTATTTTTAGTAGAGACGGGGTTTCTCCGTGTTGGTCAGGCTAGTCTCAAACTCCCAACCT T C BECN1 Ensembl:ENSG00000126581 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs952928480 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79658,RMVar_hsa_circ_184501 50601 RMVar_ID_50601 Human_SNP_ID_624734087 A-to-I Human chr17 - 42816434 42816433 42816434 TTGGCCGGACTGCTCTCGAACTCCTGACCTCAAGTTATCCACCCGTCTTGGCCTCCCAAAGTGCT TTGGCCGGACTGCTCTCGAACTCCTGACCTCA_GTTATCCACCCGTCTTGGCCTCCCAAAGTGCT CT C BECN1 Ensembl:ENSG00000126581 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs990158153 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_25285103 RMVar_hsa_circ_48256 50602 RMVar_ID_50602 Human_SNP_ID_624734088 A-to-I Human chr17 - 42816435 42816435 42816435 ATTGGCCGGACTGCTCTCGAACTCCTGACCTCAAGTTATCCACCCGTCTTGGCCTCCCAAAGTGC ATTGGCCGGACTGCTCTCGAACTCCTGACCTCGAGTTATCCACCCGTCTTGGCCTCCCAAAGTGC T C BECN1 Ensembl:ENSG00000126581 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1198286605 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13011524,Human_RBP_ID_25285103 RMVar_hsa_circ_48256 50603 RMVar_ID_50603 Human_SNP_ID_624739618 A-to-I Human chr17 + 42837656 42837656 42837656 CATCCCTGCCTCTTTGTATCCTTAGCCCACTTATAAGAAGCGAAGGTTGGATGAGTGTGAAGAAG CATCCCTGCCTCTTTGTATCCTTAGCCCACTTGTAAGAAGCGAAGGTTGGATGAGTGTGAAGAAG A G PSME3 Ensembl:ENSG00000131467 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs756349475 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_301032,Human_RBP_ID_1858575,Human_RBP_ID_2507016,Human_RBP_ID_4473434,Human_RBP_ID_5367127,Human_RBP_ID_9376065,Human_RBP_ID_13011838,Human_RBP_ID_18988551 Human_Splice_Rec_1821354,Human_Splice_Rec_1821355,Human_Splice_Rec_1821374,Human_Splice_Rec_1821375,Human_Splice_Rec_1821406,Human_Splice_Rec_1821407,Human_Splice_Rec_1821426,Human_Splice_Rec_1821427,Human_Splice_Rec_1821438,Human_Splice_Rec_1821439,Human_Splice_Rec_1821462,Human_Splice_Rec_1821463,Human_Splice_Rec_1821482,Human_Splice_Rec_1821483,Human_Splice_Rec_1821496,Human_Splice_Rec_1821497,Human_Splice_Rec_1821512,Human_Splice_Rec_1821520,Human_Splice_Rec_1821521,Human_Splice_Rec_1821538,Human_Splice_Rec_1821539,Human_Splice_Rec_1821554,Human_Splice_Rec_1821555,Human_Splice_Rec_1821576,Human_Splice_Rec_1821577,Human_Splice_Rec_1821586,Human_Splice_Rec_1821587 RMVar_hsa_circ_34295,RMVar_hsa_circ_58261,RMVar_hsa_circ_69875,RMVar_hsa_circ_285754,RMVar_hsa_circ_332895,RMVar_hsa_circ_184504,RMVar_hsa_circ_26556,RMVar_hsa_circ_184506,RMVar_hsa_circ_73383,RMVar_hsa_circ_279759,RMVar_hsa_circ_184507 50604 RMVar_ID_50604 Human_SNP_ID_624739619 A-to-I Human chr17 + 42837656 42837656 42837656 CATCCCTGCCTCTTTGTATCCTTAGCCCACTTATAAGAAGCGAAGGTTGGATGAGTGTGAAGAAG CATCCCTGCCTCTTTGTATCCTTAGCCCACTTTTAAGAAGCGAAGGTTGGATGAGTGTGAAGAAG A T PSME3 Ensembl:ENSG00000131467 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs756349475 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_301032,Human_RBP_ID_1858575,Human_RBP_ID_2507016,Human_RBP_ID_4473434,Human_RBP_ID_5367127,Human_RBP_ID_9376065,Human_RBP_ID_13011838,Human_RBP_ID_18988551 Human_Splice_Rec_1821354,Human_Splice_Rec_1821355,Human_Splice_Rec_1821374,Human_Splice_Rec_1821375,Human_Splice_Rec_1821406,Human_Splice_Rec_1821407,Human_Splice_Rec_1821426,Human_Splice_Rec_1821427,Human_Splice_Rec_1821438,Human_Splice_Rec_1821439,Human_Splice_Rec_1821462,Human_Splice_Rec_1821463,Human_Splice_Rec_1821482,Human_Splice_Rec_1821483,Human_Splice_Rec_1821496,Human_Splice_Rec_1821497,Human_Splice_Rec_1821512,Human_Splice_Rec_1821520,Human_Splice_Rec_1821521,Human_Splice_Rec_1821538,Human_Splice_Rec_1821539,Human_Splice_Rec_1821554,Human_Splice_Rec_1821555,Human_Splice_Rec_1821576,Human_Splice_Rec_1821577,Human_Splice_Rec_1821586,Human_Splice_Rec_1821587 RMVar_hsa_circ_34295,RMVar_hsa_circ_58261,RMVar_hsa_circ_69875,RMVar_hsa_circ_285754,RMVar_hsa_circ_332895,RMVar_hsa_circ_184504,RMVar_hsa_circ_26556,RMVar_hsa_circ_184506,RMVar_hsa_circ_73383,RMVar_hsa_circ_279759,RMVar_hsa_circ_184507 50605 RMVar_ID_50605 Human_SNP_ID_624755954 A-to-I Human chr17 - 42897799 42897799 42897799 GGGCCTACAGGCGCACACCACCAAACCCAGCTAACTTTTTATTTTTTGTGGAGATGGGGGTCTCT GGGCCTACAGGCGCACACCACCAAACCCAGCTGACTTTTTATTTTTTGTGGAGATGGGGGTCTCT T C LINC00671 Ensembl:ENSG00000213373 lincRNA exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs978843348 Functional Loss SNV dbSNP153 33..33 33 - - - 50606 RMVar_ID_50606 Human_SNP_ID_624769831 A-to-I Human chr17 - 42954068 42954068 42954068 ATTACAGGTGTGAGCCACTGTGTCCAGCCTGTATCTTTCTTTAGGACTGTCCCCTACCTCCTTTA ATTACAGGTGTGAGCCACTGTGTCCAGCCTGTGTCTTTCTTTAGGACTGTCCCCTACCTCCTTTA T C AARSD1,PTGES3L-AARSD1 Ensembl:ENSG00000266967,Ensembl:ENSG00000108825 Protein coding,Protein coding exon,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs7218454 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_6588,GWAS_ID_6589,GWAS_ID_6590,GWAS_ID_6591,GWAS_ID_6592,GWAS_ID_6593 RMVar_hsa_circ_95393,RMVar_hsa_circ_378621,RMVar_hsa_circ_184511 50607 RMVar_ID_50607 Human_SNP_ID_624769868 A-to-I Human chr17 - 42954299 42954299 42954299 GTGTCTGGAGTGCAGTGGCATGATCTCGGCTCAGTGTAACCTGTGCCTCCTGGGTCCAAGCGGTT GTGTCTGGAGTGCAGTGGCATGATCTCGGCTCGGTGTAACCTGTGCCTCCTGGGTCCAAGCGGTT T C AARSD1,PTGES3L-AARSD1 Ensembl:ENSG00000266967,Ensembl:ENSG00000108825 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1366647093 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22475105 RMVar_hsa_circ_95393,RMVar_hsa_circ_378621,RMVar_hsa_circ_184511 50608 RMVar_ID_50608 Human_SNP_ID_624769944 A-to-I Human chr17 - 42954559 42954559 42954559 ATGGTAGTACGCGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGAACCCG ATGGTAGTACGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGAACCCG T C AARSD1,PTGES3L-AARSD1 Ensembl:ENSG00000266967,Ensembl:ENSG00000108825 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1409534277 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95393,RMVar_hsa_circ_378621,RMVar_hsa_circ_184511 50609 RMVar_ID_50609 Human_SNP_ID_624769947 A-to-I Human chr17 - 42954573 42954573 42954573 AAAATTAGCTAGGCATGGTAGTACGCGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGA AAAATTAGCTAGGCATGGTAGTACGCGCCTGTGGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGA T C AARSD1,PTGES3L-AARSD1 Ensembl:ENSG00000266967,Ensembl:ENSG00000108825 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1419088591 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95393,RMVar_hsa_circ_378621,RMVar_hsa_circ_184511 50610 RMVar_ID_50610 Human_SNP_ID_624771381 A-to-I Human chr17 - 42959140 42959140 42959140 CAGGCTGGAGTGCAGTGGTGCAGTCTTGGCTCACTGCAACCTCTGCCTACTGGGTTCGGGTGATT CAGGCTGGAGTGCAGTGGTGCAGTCTTGGCTCGCTGCAACCTCTGCCTACTGGGTTCGGGTGATT T C AARSD1,PTGES3L-AARSD1 Ensembl:ENSG00000266967,Ensembl:ENSG00000108825 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1464160508 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27367,RMVar_hsa_circ_65655,RMVar_hsa_circ_98737,RMVar_hsa_circ_126982,RMVar_hsa_circ_21537,RMVar_hsa_circ_184514,RMVar_hsa_circ_300281,RMVar_hsa_circ_184516,RMVar_hsa_circ_95160,RMVar_hsa_circ_184517 50611 RMVar_ID_50611 Human_SNP_ID_624771646 A-to-I Human chr17 - 42960027 42960027 42960027 AGACCTCGTGATCCGCCCGCCTCGGCTTCTCAATGTGCTGAGATTACAGGCGGGAGCCACTGCGC AGACCTCGTGATCCGCCCGCCTCGGCTTCTCAGTGTGCTGAGATTACAGGCGGGAGCCACTGCGC T C AARSD1,PTGES3L-AARSD1 Ensembl:ENSG00000266967,Ensembl:ENSG00000108825 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1429731924 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27367,RMVar_hsa_circ_65655,RMVar_hsa_circ_98737,RMVar_hsa_circ_126982,RMVar_hsa_circ_21537,RMVar_hsa_circ_184514,RMVar_hsa_circ_300281,RMVar_hsa_circ_184516,RMVar_hsa_circ_95160,RMVar_hsa_circ_184517 50612 RMVar_ID_50612 Human_SNP_ID_624776810 A-to-I Human chr17 - 42976121 42976121 42976121 AAAATGAGCTGGGCGTGGTGGTGCGAGCCTGTAGTGCCAGCTACTCGGGAGGCTGAGGCGGGAGA AAAATGAGCTGGGCGTGGTGGTGCGAGCCTGTGGTGCCAGCTACTCGGGAGGCTGAGGCGGGAGA T C PTGES3L,PTGES3L-AARSD1 Ensembl:ENSG00000267060,Ensembl:ENSG00000108825 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031857318 Functional Loss SNV dbSNP153 33..33 33 - - - 50613 RMVar_ID_50613 Human_SNP_ID_624777032 A-to-I Human chr17 - 42977108 42977108 42977108 TTTTGTATTTTTAGTAGAGATGGGGTTTTGCCATGTTGACTAGGCTGGTCTCGAACTTCAGACCT TTTTGTATTTTTAGTAGAGATGGGGTTTTGCCGTGTTGACTAGGCTGGTCTCGAACTTCAGACCT T C PTGES3L,PTGES3L-AARSD1 Ensembl:ENSG00000267060,Ensembl:ENSG00000108825 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1364940822 Functional Loss SNV dbSNP153 33..33 33 - - - 50614 RMVar_ID_50614 Human_SNP_ID_624778983 A-to-I Human chr17 + 42983094 42983094 42983094 CCAACACTTGGGGAGGCGAAGGCTGGAGGAGGATCACTTGAGCCCAGGAGTTGGAGGCTGCAGAG CCAACACTTGGGGAGGCGAAGGCTGGAGGAGGTTCACTTGAGCCCAGGAGTTGGAGGCTGCAGAG A T RUNDC1 Ensembl:ENSG00000198863 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1157527941 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115857,RMVar_hsa_circ_184518 50615 RMVar_ID_50615 Human_SNP_ID_624779096 A-to-I Human chr17 + 42983488 42983488 42983488 AGCCTTGACTCCCAGGCTCAGTAGATCCTCCTACCTCAGCCTCTCGAGTAACTGGGACCACAGGC AGCCTTGACTCCCAGGCTCAGTAGATCCTCCTGCCTCAGCCTCTCGAGTAACTGGGACCACAGGC A G RUNDC1 Ensembl:ENSG00000198863 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1292853927 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13012997,Human_RBP_ID_17566861 RMVar_hsa_circ_115857,RMVar_hsa_circ_184518 50616 RMVar_ID_50616 Human_SNP_ID_624779361 A-to-I Human chr17 + 42984470 42984470 42984470 CCCCGGCTAAATTTTGTATTTTGAGTAGAGACAGGGTTTTGCCATGTTGGCCAGGCTGGTCTCGA CCCCGGCTAAATTTTGTATTTTGAGTAGAGACGGGGTTTTGCCATGTTGGCCAGGCTGGTCTCGA A G RUNDC1 Ensembl:ENSG00000198863 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1328896905 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_115857,RMVar_hsa_circ_184518 50617 RMVar_ID_50617 Human_SNP_ID_624783794 A-to-I Human chr17 + 43000783 43000783 43000783 GTGTTTTTTAAGAAGTACAAGAGGCCGGGCACAATGGCTCACGCCTGTAATCCCATCACTTTGGG GTGTTTTTTAAGAAGTACAAGAGGCCGGGCACCATGGCTCACGCCTGTAATCCCATCACTTTGGG A C RPL27 Ensembl:ENSG00000131469 Protein coding intron GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-Seq:(High) rs1369995209 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79189,RMVar_hsa_circ_114141,RMVar_hsa_circ_96940,RMVar_hsa_circ_184520,RMVar_hsa_circ_184521,RMVar_hsa_circ_94719,RMVar_hsa_circ_184523,RMVar_hsa_circ_184524 50618 RMVar_ID_50618 Human_SNP_ID_624784127 A-to-I Human chr17 + 43001948 43001948 43001948 CCCGTCTCTACTGAAAGTACAAAAAATTAGCCAGGCATGGTGGCAGGCGCCTGTAGTAGTCCCAG CCCGTCTCTACTGAAAGTACAAAAAATTAGCCGGGCATGGTGGCAGGCGCCTGTAGTAGTCCCAG A G RPL27 Ensembl:ENSG00000131469 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs690936 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79189,RMVar_hsa_circ_114141,RMVar_hsa_circ_96940,RMVar_hsa_circ_184520,RMVar_hsa_circ_184521,RMVar_hsa_circ_94719,RMVar_hsa_circ_184523,RMVar_hsa_circ_184524 50619 RMVar_ID_50619 Human_SNP_ID_624786240 A-to-I Human chr17 + 43008316 43008316 43008316 TCAAGCTCCCAAAGTGCTGGGATTACAGGTGTAAGCCACCATGCCCGGACTTTTCTTTCCTTTTT TCAAGCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCATGCCCGGACTTTTCTTTCCTTTTT A G IFI35 Ensembl:ENSG00000068079 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1195471381 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_116856,RMVar_hsa_circ_184527 50620 RMVar_ID_50620 Human_SNP_ID_624786304 A-to-I Human chr17 + 43008448 43008441 43008448 TTGGCTCACTGCAACCTCTGCCTTCCAGATTCAAGTGATTCTCTTGCCTCAGCATCCCAAGTAGC TTGGCTCACTGCAACCTCTGCCTTCC_______AGTGATTCTCTTGCCTCAGCATCCCAAGTAGC CAGATTCA C IFI35 Ensembl:ENSG00000068079 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1567742011 Functional Loss DEL dbSNP153 27..33 33 - - - Human_RBP_ID_13013761 RMVar_hsa_circ_116856,RMVar_hsa_circ_184527 50621 RMVar_ID_50621 Human_SNP_ID_624796206 A-to-I Human chr17 - 43044920 43044920 43044920 GGACACCTGTAATCCCAGCTACTCAGGTGGCTAAGGCAGGAGAATCACTTCAGCCCGGGAGGTGG GGACACCTGTAATCCCAGCTACTCAGGTGGCTGAGGCAGGAGAATCACTTCAGCCCGGGAGGTGG T C BRCA1 Ensembl:ENSG00000012048 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1342609245 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22588147,Human_RBP_ID_25285686 RMVar_hsa_circ_184540,RMVar_hsa_circ_101058,RMVar_hsa_circ_269613 50622 RMVar_ID_50622 Human_SNP_ID_624796226 A-to-I Human chr17 - 43044968 43044968 43044968 GAAACCCCATCTCTACTAAAAATACAGAAATTAGCCGGTCATGGTGGTGGACACCTGTAATCCCA GAAACCCCATCTCTACTAAAAATACAGAAATTTGCCGGTCATGGTGGTGGACACCTGTAATCCCA T A BRCA1 Ensembl:ENSG00000012048 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1255825310 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_184540,RMVar_hsa_circ_101058,RMVar_hsa_circ_269613 50623 RMVar_ID_50623 Human_SNP_ID_624798001 A-to-I Human chr17 - 43050419 43050419 43050419 TTTTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAATATGGTCCCGATCTCCTGACCTCGTGA TTTTTTTAGTAGAGACGGGGTTTCACCGTGTTCGCCAATATGGTCCCGATCTCCTGACCTCGTGA T G BRCA1 Ensembl:ENSG00000012048 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1390738562 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_8450,RMVar_hsa_circ_25436,RMVar_hsa_circ_316549,RMVar_hsa_circ_184540,RMVar_hsa_circ_101058,RMVar_hsa_circ_269613,RMVar_hsa_circ_328786,RMVar_hsa_circ_184541,RMVar_hsa_circ_316568,RMVar_hsa_circ_273846,RMVar_hsa_circ_291899,RMVar_hsa_circ_29983,RMVar_hsa_circ_184542,RMVar_hsa_circ_184543,RMVar_hsa_circ_184544,RMVar_hsa_circ_300633,RMVar_hsa_circ_329161,RMVar_hsa_circ_343956,RMVar_hsa_circ_318144,RMVar_hsa_circ_23036,RMVar_hsa_circ_184545,RMVar_hsa_circ_184546,RMVar_hsa_circ_184547 50624 RMVar_ID_50624 Human_SNP_ID_624800384 A-to-I Human chr17 - 43059411 43059411 43059411 CTAGAGTGCATGGAGTGCGGTAGCACGATCTCAGCTCACTCCAACCTCCGCCTCCCGGTTCAAGT CTAGAGTGCATGGAGTGCGGTAGCACGATCTCGGCTCACTCCAACCTCCGCCTCCCGGTTCAAGT T C BRCA1 Ensembl:ENSG00000012048 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs570221030 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25436,RMVar_hsa_circ_316549,RMVar_hsa_circ_184540,RMVar_hsa_circ_101058,RMVar_hsa_circ_269613,RMVar_hsa_circ_328786,RMVar_hsa_circ_184541,RMVar_hsa_circ_316568,RMVar_hsa_circ_291899,RMVar_hsa_circ_29983,RMVar_hsa_circ_184542,RMVar_hsa_circ_184543,RMVar_hsa_circ_300633,RMVar_hsa_circ_343956,RMVar_hsa_circ_318144,RMVar_hsa_circ_23036,RMVar_hsa_circ_66795,RMVar_hsa_circ_184546,RMVar_hsa_circ_184547,RMVar_hsa_circ_306925,RMVar_hsa_circ_288482,RMVar_hsa_circ_365665,RMVar_hsa_circ_184549,RMVar_hsa_circ_33256 50625 RMVar_ID_50625 Human_SNP_ID_624804778 A-to-I Human chr17 - 43074487 43074487 43074487 CATCCCCTTCTAAATGCCCATCATTAGATGATAGGTGGTACATGCACAGTTGCTCTGGGAGTCTT CATCCCCTTCTAAATGCCCATCATTAGATGATGGGTGGTACATGCACAGTTGCTCTGGGAGTCTT T C BRCA1 Ensembl:ENSG00000012048 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1567778299 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1858825,Human_RBP_ID_4429394,Human_RBP_ID_6596767,Human_RBP_ID_13014634,Human_RBP_ID_20217479 Human_Splice_Rec_1822260,Human_Splice_Rec_1822302,Human_Splice_Rec_1822348,Human_Splice_Rec_1822392,Human_Splice_Rec_1822418,Human_Splice_Rec_1822452,Human_Splice_Rec_1822502,Human_Splice_Rec_1822546,Human_Splice_Rec_1822590,Human_Splice_Rec_1822622,Human_Splice_Rec_1822656,Human_Splice_Rec_1822688 Clinvar_Rec_137 RMVar_hsa_circ_25436,RMVar_hsa_circ_184540,RMVar_hsa_circ_101058,RMVar_hsa_circ_269613,RMVar_hsa_circ_328786,RMVar_hsa_circ_184541,RMVar_hsa_circ_291899,RMVar_hsa_circ_29983,RMVar_hsa_circ_184542,RMVar_hsa_circ_343956,RMVar_hsa_circ_318144,RMVar_hsa_circ_66795,RMVar_hsa_circ_184547,RMVar_hsa_circ_365665,RMVar_hsa_circ_33256,RMVar_hsa_circ_320880,RMVar_hsa_circ_51168,RMVar_hsa_circ_47031,RMVar_hsa_circ_103692,RMVar_hsa_circ_184551,RMVar_hsa_circ_347593,RMVar_hsa_circ_184550,RMVar_hsa_circ_281254,RMVar_hsa_circ_68118,RMVar_hsa_circ_272793,RMVar_hsa_circ_25916,RMVar_hsa_circ_374017,RMVar_hsa_circ_184552,RMVar_hsa_circ_51021,RMVar_hsa_circ_184553 50626 RMVar_ID_50626 Human_SNP_ID_624806385 A-to-I Human chr17 - 43080687 43080687 43080687 CTCCTGCCTTAGCCTCCCAAGTAGCTGGGACTATAGGCGTCCACCACCATACCCAGCTAATTTTT CTCCTGCCTTAGCCTCCCAAGTAGCTGGGACTGTAGGCGTCCACCACCATACCCAGCTAATTTTT T C BRCA1 Ensembl:ENSG00000012048 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1057479808 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25436,RMVar_hsa_circ_184540,RMVar_hsa_circ_101058,RMVar_hsa_circ_269613,RMVar_hsa_circ_328786,RMVar_hsa_circ_184541,RMVar_hsa_circ_29983,RMVar_hsa_circ_184542,RMVar_hsa_circ_343956,RMVar_hsa_circ_66795,RMVar_hsa_circ_184547,RMVar_hsa_circ_33256,RMVar_hsa_circ_51168,RMVar_hsa_circ_47031,RMVar_hsa_circ_347593,RMVar_hsa_circ_68118,RMVar_hsa_circ_69334,RMVar_hsa_circ_25916,RMVar_hsa_circ_374017,RMVar_hsa_circ_336993,RMVar_hsa_circ_184553,RMVar_hsa_circ_360221,RMVar_hsa_circ_296660 50627 RMVar_ID_50627 Human_SNP_ID_624818722 A-to-I Human chr17 - 43113523 43113523 43113523 CTCTACTAAAACACACAAAAAACTAGCCTGGCATGGTGGCACGTACCTGTAGTCCCAGCTACTTG CTCTACTAAAACACACAAAAAACTAGCCTGGCGTGGTGGCACGTACCTGTAGTCCCAGCTACTTG T C BRCA1 Ensembl:ENSG00000012048 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1176563287 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_184540,RMVar_hsa_circ_101058,RMVar_hsa_circ_328786,RMVar_hsa_circ_29983,RMVar_hsa_circ_184542,RMVar_hsa_circ_68118,RMVar_hsa_circ_25916,RMVar_hsa_circ_336993,RMVar_hsa_circ_336194,RMVar_hsa_circ_51267,RMVar_hsa_circ_184554,RMVar_hsa_circ_64883,RMVar_hsa_circ_104161,RMVar_hsa_circ_184556,RMVar_hsa_circ_272056,RMVar_hsa_circ_46961,RMVar_hsa_circ_184557,RMVar_hsa_circ_280714,RMVar_hsa_circ_360380,RMVar_hsa_circ_326262,RMVar_hsa_circ_184560,RMVar_hsa_circ_53845,RMVar_hsa_circ_335543,RMVar_hsa_circ_349624 50628 RMVar_ID_50628 Human_SNP_ID_624819560 A-to-I Human chr17 - 43116615 43116610 43116616 ACCTGGGAGGCTGAGGCAGGAGAATCACTTGAACTTGGGAGGCAGAGGTTGCAGTGAGCCGAGAT ACCTGGGAGGCTGAGGCAGGAGAATCACTTG______GGAGGCAGAGGTTGCAGTGAGCCGAGAT CCAAGTT C BRCA1 Ensembl:ENSG00000012048 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs796069013 Functional Loss DEL dbSNP153 32..37 33 - - - RMVar_hsa_circ_328786,RMVar_hsa_circ_184542,RMVar_hsa_circ_68118,RMVar_hsa_circ_336993,RMVar_hsa_circ_51267,RMVar_hsa_circ_272056,RMVar_hsa_circ_184557,RMVar_hsa_circ_280714,RMVar_hsa_circ_360380,RMVar_hsa_circ_335543,RMVar_hsa_circ_184562,RMVar_hsa_circ_297919 50629 RMVar_ID_50629 Human_SNP_ID_624820150 A-to-I Human chr17 - 43119055 43119055 43119055 ATCCAAAAAATCCGTTTCAAAAATTCACATTTAGAGCTAAGTGTAGTGGCTCACGCCTGTAATCC ATCCAAAAAATCCGTTTCAAAAATTCACATTTGGAGCTAAGTGTAGTGGCTCACGCCTGTAATCC T C BRCA1 Ensembl:ENSG00000012048 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1162902395 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_328786,RMVar_hsa_circ_184542,RMVar_hsa_circ_68118,RMVar_hsa_circ_336993,RMVar_hsa_circ_51267,RMVar_hsa_circ_272056,RMVar_hsa_circ_184557,RMVar_hsa_circ_280714,RMVar_hsa_circ_360380,RMVar_hsa_circ_335543,RMVar_hsa_circ_184562,RMVar_hsa_circ_297919 50630 RMVar_ID_50630 Human_SNP_ID_624821091 A-to-I Human chr17 - 43122706 43122706 43122706 TAGGGTTTTGCTATGTTGGCCATGCTGGTCTCAAACTCCTGACCTCAAGTGATCTACCCTCCCTT TAGGGTTTTGCTATGTTGGCCATGCTGGTCTCTAACTCCTGACCTCAAGTGATCTACCCTCCCTT T A BRCA1 Ensembl:ENSG00000012048 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs765422008 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_328786,RMVar_hsa_circ_184542,RMVar_hsa_circ_68118,RMVar_hsa_circ_336993,RMVar_hsa_circ_51267,RMVar_hsa_circ_272056,RMVar_hsa_circ_184557,RMVar_hsa_circ_280714,RMVar_hsa_circ_360380,RMVar_hsa_circ_335543,RMVar_hsa_circ_184562,RMVar_hsa_circ_297919 50631 RMVar_ID_50631 Human_SNP_ID_624821092 A-to-I Human chr17 - 43122706 43122706 43122706 TAGGGTTTTGCTATGTTGGCCATGCTGGTCTCAAACTCCTGACCTCAAGTGATCTACCCTCCCTT TAGGGTTTTGCTATGTTGGCCATGCTGGTCTCCAACTCCTGACCTCAAGTGATCTACCCTCCCTT T G BRCA1 Ensembl:ENSG00000012048 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs765422008 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_328786,RMVar_hsa_circ_184542,RMVar_hsa_circ_68118,RMVar_hsa_circ_336993,RMVar_hsa_circ_51267,RMVar_hsa_circ_272056,RMVar_hsa_circ_184557,RMVar_hsa_circ_280714,RMVar_hsa_circ_360380,RMVar_hsa_circ_335543,RMVar_hsa_circ_184562,RMVar_hsa_circ_297919 50632 RMVar_ID_50632 Human_SNP_ID_624821373 A-to-I Human chr17 - 43123523 43123523 43123523 CAACATGGTGAAACCCCCTCTCCACTAAAAATACAAAAATTAGCTGGGCGTAGTGGCATGTGCCT CAACATGGTGAAACCCCCTCTCCACTAAAAATTCAAAAATTAGCTGGGCGTAGTGGCATGTGCCT T A BRCA1 Ensembl:ENSG00000012048 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1247459403 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_328786,RMVar_hsa_circ_184542,RMVar_hsa_circ_68118,RMVar_hsa_circ_336993,RMVar_hsa_circ_51267,RMVar_hsa_circ_272056,RMVar_hsa_circ_184557,RMVar_hsa_circ_280714,RMVar_hsa_circ_360380,RMVar_hsa_circ_335543,RMVar_hsa_circ_184562,RMVar_hsa_circ_297919 50633 RMVar_ID_50633 Human_SNP_ID_624821617 A-to-I Human chr17 - 43124117 43124117 43124117 AGATATATATATATGTTTTTCTAATGTGTTAAAGTTCATTGGAACAGAAAGAAATGGATTTATCT AGATATATATATATGTTTTTCTAATGTGTTAAGGTTCATTGGAACAGAAAGAAATGGATTTATCT T C BRCA1 Ensembl:ENSG00000012048 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs886040902 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1858888,Human_RBP_ID_3524016,Human_RBP_ID_4473596,Human_RBP_ID_17609696,Human_RBP_ID_25286294 Clinvar_Rec_138 50634 RMVar_ID_50634 Human_SNP_ID_624821810 A-to-I Human chr17 - 43124925 43124925 43124925 CCTGACCAACGTGGTGAAACTCCGTCTCTACTAAAAATACAAAAATTAGCCGGGCGTGGTGCCGC CCTGACCAACGTGGTGAAACTCCGTCTCTACTGAAAATACAAAAATTAGCCGGGCGTGGTGCCGC T C BRCA1 Ensembl:ENSG00000012048 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1489102499 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_132929 50635 RMVar_ID_50635 Human_SNP_ID_624823877 A-to-I Human chr17 + 43131858 43131858 43131858 CAGGCTGCAGTGCAGTGGCGCAATCTCAGCTCACTGCAACCTCTGCTTCCTGGGTTGAAGCGATT CAGGCTGCAGTGCAGTGGCGCAATCTCAGCTCGCTGCAACCTCTGCTTCCTGGGTTGAAGCGATT A G NBR2 Ensembl:ENSG00000198496 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs942919643 Functional Loss SNV dbSNP153 33..33 33 - - - 50636 RMVar_ID_50636 Human_SNP_ID_624824991 A-to-I Human chr17 + 43136022 43136022 43136022 TAAAAGGGCTTAATACAGGCTTCGCCGGGCGCAGGGCTCCCGCCTGTAATTCCAGTACTTTGGGA TAAAAGGGCTTAATACAGGCTTCGCCGGGCGCGGGGCTCCCGCCTGTAATTCCAGTACTTTGGGA A G NBR2 Ensembl:ENSG00000198496 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs988536331 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6596995,Human_RBP_ID_13015759,Human_RBP_ID_18698639,Human_RBP_ID_22357281 50637 RMVar_ID_50637 Human_SNP_ID_624826407 A-to-I Human chr17 + 43141560 43141560 43141560 AATTATCACCGGGCACGGTGGCTCACACCTGTAATCCAGCACTTTGGGAGGCTGAGGCGGGCGGA AATTATCACCGGGCACGGTGGCTCACACCTGTCATCCAGCACTTTGGGAGGCTGAGGCGGGCGGA A C NBR2 Ensembl:ENSG00000198496 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1438801476 Functional Loss SNV dbSNP153 33..33 33 - - - 50638 RMVar_ID_50638 Human_SNP_ID_624826516 A-to-I Human chr17 + 43142015 43142015 43142015 CTCACTGCAACCTCCGTCTCCTGGGTTCAAGCAATTCTCCCTGCTTCAGCCTCCTGAGTAACTGG CTCACTGCAACCTCCGTCTCCTGGGTTCAAGCGATTCTCCCTGCTTCAGCCTCCTGAGTAACTGG A G NBR2 Ensembl:ENSG00000198496 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs916946650 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17565935 50639 RMVar_ID_50639 Human_SNP_ID_624826884 A-to-I Human chr17 + 43143221 43143221 43143221 CCTTGGCCTCCCAAAATGTTGGGATTACAGGCATAAACCACCATGCCCGGCCTAGTCTTGTGCTT CCTTGGCCTCCCAAAATGTTGGGATTACAGGCGTAAACCACCATGCCCGGCCTAGTCTTGTGCTT A G NBR2 Ensembl:ENSG00000198496 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs996741822 Functional Loss SNV dbSNP153 33..33 33 - - - 50640 RMVar_ID_50640 Human_SNP_ID_624827712 A-to-I Human chr17 + 43146515 43146515 43146515 TATTTTTAGTAGAGACGGGGTTTCACTGTATTAGCCAGGATGGTCTCGATCTCCTGACCTCGTGA TATTTTTAGTAGAGACGGGGTTTCACTGTATTGGCCAGGATGGTCTCGATCTCCTGACCTCGTGA A G NBR2 Ensembl:ENSG00000198496 lincRNA intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1470927904 Functional Loss SNV dbSNP153 33..33 33 - - - 50641 RMVar_ID_50641 Human_SNP_ID_624832541 A-to-I Human chr17 - 43167773 43167773 43167773 AATGAGGCCGGGGGCTGTGGCTCACACCTGTAATCCCAGCACTCTGGGGGGCCGAGGCAGGCAGA AATGAGGCCGGGGGCTGTGGCTCACACCTGTACTCCCAGCACTCTGGGGGGCCGAGGCAGGCAGA T G AC060780.1,BRCA1 Ensembl:ENSG00000267002,Ensembl:ENSG00000012048 lincRNA,Protein coding exon,intron GSE123020:GSM3490829,GSM3490830,GSM3490831 esophageal squamous carcinoma cells,EC109 cell line - 32596459 RNA-Seq:(High) rs755256205 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1546656,Human_RBP_ID_3548435,Human_RBP_ID_13016129 Human_Splice_Rec_1822956,Human_Splice_Rec_1822964,Human_Splice_Rec_1822965,Human_Splice_Rec_1822978 Human_miRNA_ID_2775587,Human_miRNA_ID_3195465 RMVar_hsa_circ_124262,RMVar_hsa_circ_184563 50642 RMVar_ID_50642 Human_SNP_ID_624832543 A-to-I Human chr17 - 43167780 43167779 43167780 AATCATGAATGAGGCCGGGGGCTGTGGCTCACACCTGTAATCCCAGCACTCTGGGGGGCCGAGGC AATCATGAATGAGGCCGGGGGCTGTGGCTCAC_CCTGTAATCCCAGCACTCTGGGGGGCCGAGGC GT G AC060780.1,BRCA1 Ensembl:ENSG00000267002,Ensembl:ENSG00000012048 lincRNA,Protein coding exon,intron GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831 HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line - 29129909,32596459 RNA-Seq:(High) rs878950033 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_1546656,Human_RBP_ID_3548435,Human_RBP_ID_13016129 Human_Splice_Rec_1822956,Human_Splice_Rec_1822964,Human_Splice_Rec_1822965,Human_Splice_Rec_1822978 Human_miRNA_ID_2775587,Human_miRNA_ID_2891034,Human_miRNA_ID_3195465,Human_miRNA_ID_3202564 RMVar_hsa_circ_124262,RMVar_hsa_circ_184563 50643 RMVar_ID_50643 Human_SNP_ID_624832721 A-to-I Human chr17 - 43168475 43168475 43168475 CCACCATGCCTGGCTCATTTTTTTGTATTTTTAGTAGAAACGAGGTTTCTCCGTATTGGTCAGGC CCACCATGCCTGGCTCATTTTTTTGTATTTTTGGTAGAAACGAGGTTTCTCCGTATTGGTCAGGC T C AC060780.1,BRCA1 Ensembl:ENSG00000267002,Ensembl:ENSG00000012048 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1279692517 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13016140 RMVar_hsa_circ_124262,RMVar_hsa_circ_184563 50644 RMVar_ID_50644 Human_SNP_ID_624832724 A-to-I Human chr17 - 43168481 43168481 43168481 CATGCACCACCATGCCTGGCTCATTTTTTTGTATTTTTAGTAGAAACGAGGTTTCTCCGTATTGG CATGCACCACCATGCCTGGCTCATTTTTTTGTGTTTTTAGTAGAAACGAGGTTTCTCCGTATTGG T C AC060780.1,BRCA1 Ensembl:ENSG00000267002,Ensembl:ENSG00000012048 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1036147397 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13016140 RMVar_hsa_circ_124262,RMVar_hsa_circ_184563 50645 RMVar_ID_50645 Human_SNP_ID_624832903 A-to-I Human chr17 - 43169302 43169302 43169302 TAGCCGGGCGTGGTGGCGCGCGCCAGCTACTCAGGAGCTGAGGCAGGAGAATCGCTTGAACCCAG TAGCCGGGCGTGGTGGCGCGCGCCAGCTACTCGGGAGCTGAGGCAGGAGAATCGCTTGAACCCAG T C AC060780.1,BRCA1 Ensembl:ENSG00000267002,Ensembl:ENSG00000012048 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1383398700 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3549256 RMVar_hsa_circ_124262,RMVar_hsa_circ_184563 50646 RMVar_ID_50646 Human_SNP_ID_624832938 A-to-I Human chr17 - 43169440 43169440 43169440 GCTGGTCGCCGGGGATGGTGGCTTACGCCTGTATTCCTAGCACTTTGGGAGGCCAAGGCGGATGG GCTGGTCGCCGGGGATGGTGGCTTACGCCTGTGTTCCTAGCACTTTGGGAGGCCAAGGCGGATGG T C AC060780.1,BRCA1 Ensembl:ENSG00000267002,Ensembl:ENSG00000012048 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1295732029 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124262,RMVar_hsa_circ_184563 50647 RMVar_ID_50647 Human_SNP_ID_624840484 A-to-I Human chr17 + 43199476 43199476 43199476 GCTGACTGCAACCTCCGCCTTCCCAGGTTCACACCATTCTCCTGCCTCAGCCTCCCGAGTAGCTG GCTGACTGCAACCTCCGCCTTCCCAGGTTCACGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTG A G NBR1 Ensembl:ENSG00000188554 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1439345089 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67132,RMVar_hsa_circ_73235,RMVar_hsa_circ_184570,RMVar_hsa_circ_24888,RMVar_hsa_circ_372724,RMVar_hsa_circ_111325,RMVar_hsa_circ_184571,RMVar_hsa_circ_184573,RMVar_hsa_circ_328568,RMVar_hsa_circ_19491,RMVar_hsa_circ_339976 50648 RMVar_ID_50648 Human_SNP_ID_624845237 A-to-I Human chr17 + 43218610 43218610 43218610 TTGAAACCGGAAGGCAGAGGTTGCAGTGAGCCAAGATCGTGCAACTGCACTCCAGCCTGGGCAAA TTGAAACCGGAAGGCAGAGGTTGCAGTGAGCCGAGATCGTGCAACTGCACTCCAGCCTGGGCAAA A G TMEM106A Ensembl:ENSG00000184988 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1046497899 Functional Loss SNV dbSNP153 33..33 33 - - - 50649 RMVar_ID_50649 Human_SNP_ID_624845426 A-to-I Human chr17 + 43219478 43219478 43219478 TCTTACAGCTGGGTGCAGTGGTATATACCTGTAGTCCCAGCTACTCAGGAAGCTGAGGTGAGAGG TCTTACAGCTGGGTGCAGTGGTATATACCTGTGGTCCCAGCTACTCAGGAAGCTGAGGTGAGAGG A G TMEM106A Ensembl:ENSG00000184988 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1138987 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_275884 50650 RMVar_ID_50650 Human_SNP_ID_624846094 A-to-I Human chr17 + 43222447 43222447 43222447 CCTCGGCCTCCCAAAGTGCTGGGATTTCAGGCATGGGCCCCTGCGCCTGGCCCCTTTCCTTTATT CCTCGGCCTCCCAAAGTGCTGGGATTTCAGGCTTGGGCCCCTGCGCCTGGCCCCTTTCCTTTATT A T lnc-LINC00854-1-001 RNACentral:URS00009AE32C lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1408435368 Functional Loss SNV dbSNP153 33..33 33 - - - 50651 RMVar_ID_50651 Human_SNP_ID_624847185 A-to-I Human chr17 + 43226073 43226073 43226073 TCTAATAGCCACATAGAAGAAGAAATAGGGCCAGGCACAGTGGCACATGCCTGTAATCCACGCTT TCTAATAGCCACATAGAAGAAGAAATAGGGCCGGGCACAGTGGCACATGCCTGTAATCCACGCTT A G lnc-LINC00854-1-001 RNACentral:URS00009AE32C lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1286759413 Functional Loss SNV dbSNP153 33..33 33 - - - 50652 RMVar_ID_50652 Human_SNP_ID_624847657 A-to-I Human chr17 + 43227686 43227686 43227686 TTTTGTACTTTTAGTAGAGACCAGGTTTCGCCATGTTGGCCAGGCTGGTCTTGAACTCCTGACCT TTTTGTACTTTTAGTAGAGACCAGGTTTCGCCGTGTTGGCCAGGCTGGTCTTGAACTCCTGACCT A G lnc-LINC00854-1-001 RNACentral:URS00009AE32C lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1319889035 Functional Loss SNV dbSNP153 33..33 33 - - - 50653 RMVar_ID_50653 Human_SNP_ID_624857461 A-to-I Human chr17 - 43318698 43318698 43318698 TGGGGTTTCACTATGTTGGCCAGACTGGTCTCAAACTCCCGAACTCAGATGATCTGCCTGCCTTG TGGGGTTTCACTATGTTGGCCAGACTGGTCTCGAACTCCCGAACTCAGATGATCTGCCTGCCTTG T C lnc-LINC00854-1-001,lnc-LINC00854-1-001:2 RNACentral:URS00009C15C1,RNACentral:URS00009BDFAF lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs996575937 Functional Loss SNV dbSNP153 33..33 33 - - - 50654 RMVar_ID_50654 Human_SNP_ID_624857462 A-to-I Human chr17 - 43318698 43318698 43318698 TGGGGTTTCACTATGTTGGCCAGACTGGTCTCAAACTCCCGAACTCAGATGATCTGCCTGCCTTG TGGGGTTTCACTATGTTGGCCAGACTGGTCTCCAACTCCCGAACTCAGATGATCTGCCTGCCTTG T G lnc-LINC00854-1-001,lnc-LINC00854-1-001:2 RNACentral:URS00009C15C1,RNACentral:URS00009BDFAF lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs996575937 Functional Loss SNV dbSNP153 33..33 33 - - - 50655 RMVar_ID_50655 Human_SNP_ID_624876243 A-to-I Human chr17 - 43377164 43377164 43377164 GTGATTCTTGTGCCTCAGCCTCTGGAGTATCTAGGATCACAGGTGCGTGCCACCATGTCTGGCTA GTGATTCTTGTGCCTCAGCCTCTGGAGTATCTGGGATCACAGGTGCGTGCCACCATGTCTGGCTA T C LINC00910 Ensembl:ENSG00000188825 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs911291671 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75040,RMVar_hsa_circ_358390 50656 RMVar_ID_50656 Human_SNP_ID_624879429 A-to-I Human chr17 - 43388705 43388705 43388705 TGTCTGGTGTCAGCCTCCTGCCTGGCAGAGGAACTCCAGCCCCTGCTCCCCGAAGCTCCTCCAGG TGTCTGGTGTCAGCCTCCTGCCTGGCAGAGGAGCTCCAGCCCCTGCTCCCCGAAGCTCCTCCAGG T C LINC00910 Ensembl:ENSG00000188825 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs4986155 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_238417,Human_RBP_ID_819647,Human_RBP_ID_2507683,Human_RBP_ID_3547977,Human_RBP_ID_6597470,Human_RBP_ID_8193854,Human_RBP_ID_8453393 50657 RMVar_ID_50657 Human_SNP_ID_624879478 A-to-I Human chr17 - 43388862 43388862 43388862 GAGGGTAAAGGAATCCACGTCCCAAGCAGAGAAGCAGCTTTCCCTACACAGCACAGGACACGGTC GAGGGTAAAGGAATCCACGTCCCAAGCAGAGAGGCAGCTTTCCCTACACAGCACAGGACACGGTC T C LINC00910 Ensembl:ENSG00000188825 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs62080667 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_819648,Human_RBP_ID_1546898,Human_RBP_ID_2529635,Human_RBP_ID_5649201,Human_RBP_ID_8193855 Human_miRNA_ID_3173821,Human_miRNA_ID_3173993,Human_miRNA_ID_3174164,Human_miRNA_ID_3174333,Human_miRNA_ID_3186603 50658 RMVar_ID_50658 Human_SNP_ID_624879482 A-to-I Human chr17 - 43388871 43388871 43388871 GGCGAGGAGGAGGGTAAAGGAATCCACGTCCCAAGCAGAGAAGCAGCTTTCCCTACACAGCACAG GGCGAGGAGGAGGGTAAAGGAATCCACGTCCCGAGCAGAGAAGCAGCTTTCCCTACACAGCACAG T C LINC00910 Ensembl:ENSG00000188825 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs62080668 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_819648,Human_RBP_ID_2529635,Human_RBP_ID_5649201 Human_miRNA_ID_3173821,Human_miRNA_ID_3173993,Human_miRNA_ID_3174164,Human_miRNA_ID_3174333,Human_miRNA_ID_3186603 50659 RMVar_ID_50659 Human_SNP_ID_624879521 A-to-I Human chr17 - 43389003 43389003 43389003 GAGGTGCGATGAAATACACAGGAGGGCTGCTAATCACATATGGGGTGGGTGCCGAGGGCCCTTAA GAGGTGCGATGAAATACACAGGAGGGCTGCTAGTCACATATGGGGTGGGTGCCGAGGGCCCTTAA T C LINC00910 Ensembl:ENSG00000188825 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs77256558 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_819649,Human_RBP_ID_2507693,Human_RBP_ID_5097959,Human_RBP_ID_5649201,Human_RBP_ID_6597475,Human_RBP_ID_13017068 50660 RMVar_ID_50660 Human_SNP_ID_624879522 A-to-I Human chr17 - 43389003 43389003 43389003 GAGGTGCGATGAAATACACAGGAGGGCTGCTAATCACATATGGGGTGGGTGCCGAGGGCCCTTAA GAGGTGCGATGAAATACACAGGAGGGCTGCTACTCACATATGGGGTGGGTGCCGAGGGCCCTTAA T G LINC00910 Ensembl:ENSG00000188825 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs77256558 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_819649,Human_RBP_ID_2507693,Human_RBP_ID_5097959,Human_RBP_ID_5649201,Human_RBP_ID_6597475,Human_RBP_ID_13017068 50661 RMVar_ID_50661 Human_SNP_ID_624908239 A-to-I Human chr17 + 43501668 43501668 43501668 ACCACGCCTAGCTAATTTTTTGTATTTTTAGTAGAGACGAGGTTCCTCCATGTTGGTCAGGCTGG ACCACGCCTAGCTAATTTTTTGTATTTTTAGTTGAGACGAGGTTCCTCCATGTTGGTCAGGCTGG A T DHX8 Ensembl:ENSG00000067596 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs915535693 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13017425 RMVar_hsa_circ_368031,RMVar_hsa_circ_55471,RMVar_hsa_circ_55297,RMVar_hsa_circ_64137,RMVar_hsa_circ_78396,RMVar_hsa_circ_107014,RMVar_hsa_circ_184582,RMVar_hsa_circ_57136,RMVar_hsa_circ_184583,RMVar_hsa_circ_344766,RMVar_hsa_circ_184584,RMVar_hsa_circ_184587,RMVar_hsa_circ_54048,RMVar_hsa_circ_87702,RMVar_hsa_circ_297971,RMVar_hsa_circ_61218,RMVar_hsa_circ_184589,RMVar_hsa_circ_41518,RMVar_hsa_circ_184588,RMVar_hsa_circ_184586,RMVar_hsa_circ_108963,RMVar_hsa_circ_184590 50662 RMVar_ID_50662 Human_SNP_ID_624945977 A-to-I Human chr17 - 43651132 43651132 43651132 TTGTATTTTTAGTGGAGATGGGGTTTCACCATATTAGCCAGGATGGTCTCGATCTCCTGATCTCG TTGTATTTTTAGTGGAGATGGGGTTTCACCATGTTAGCCAGGATGGTCTCGATCTCCTGATCTCG T C MEOX1 Ensembl:ENSG00000005102 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs998404442 Functional Loss SNV dbSNP153 33..33 33 - - - 50663 RMVar_ID_50663 Human_SNP_ID_624947068 A-to-I Human chr17 - 43655388 43655388 43655388 CGGCTCACTGCAACCTCCGCCTCCCGTATTCAAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGCT CGGCTCACTGCAACCTCCGCCTCCCGTATTCACGTGATTCTCCTGCCTCAGCCTCCCAAGTAGCT T G MEOX1 Ensembl:ENSG00000005102 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223629537 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_132808 50664 RMVar_ID_50664 Human_SNP_ID_624970290 A-to-I Human chr17 - 43754588 43754584 43754588 TGCTCTCTTCTGACAGCCAAAGATGAAAAACAAACAGAAAAAAAAAAGTAAAGAGTCTATTTATG TGCTCTCTTCTGACAGCCAAAGATGAAAAACA____GAAAAAAAAAAGTAAAGAGTCTATTTATG CTGTT C SOST Ensembl:ENSG00000167941 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs200132741 Functional Loss DEL dbSNP153 33..36 33 - - - 50665 RMVar_ID_50665 Human_SNP_ID_624970295 A-to-I Human chr17 - 43754588 43754588 43754588 TGCTCTCTTCTGACAGCCAAAGATGAAAAACAAACAGAAAAAAAAAAGTAAAGAGTCTATTTATG TGCTCTCTTCTGACAGCCAAAGATGAAAAACAGACAGAAAAAAAAAAGTAAAGAGTCTATTTATG T C SOST Ensembl:ENSG00000167941 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs199560099 Functional Loss SNV dbSNP153 33..33 33 - - - 50666 RMVar_ID_50666 Human_SNP_ID_624975904 A-to-I Human chr17 - 43777101 43777101 43777101 GGGCATGGTGCCTGGCGCCTGTGATCCCAGCTACTCCGGAGGCTGAGGCAGGAGAATCGTTTGAA GGGCATGGTGCCTGGCGCCTGTGATCCCAGCTCCTCCGGAGGCTGAGGCAGGAGAATCGTTTGAA T G DUSP3 Ensembl:ENSG00000108861 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs988143391 Functional Loss SNV dbSNP153 33..33 33 - - - 50667 RMVar_ID_50667 Human_SNP_ID_624975935 A-to-I Human chr17 - 43777264 43777264 43777264 TGTTGAATTATTAATAGTATTAGAGGCCTGGCACGATGGCTCACGCCTGTAATCCCAGCACTTTG TGTTGAATTATTAATAGTATTAGAGGCCTGGCGCGATGGCTCACGCCTGTAATCCCAGCACTTTG T C DUSP3 Ensembl:ENSG00000108861 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs571829517 Functional Loss SNV dbSNP153 33..33 33 - - - 50668 RMVar_ID_50668 Human_SNP_ID_624982561 A-to-I Human chr17 - 43806897 43806897 43806897 TCATTTAGAAACATACAATATTGGCTGGGTGCAGTGGCTCACACCTGTAATCCCAACACTTTGGA TCATTTAGAAACATACAATATTGGCTGGGTGCCGTGGCTCACACCTGTAATCCCAACACTTTGGA T G MPP3 Ensembl:ENSG00000161647 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs963905593 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99276,RMVar_hsa_circ_184611 50669 RMVar_ID_50669 Human_SNP_ID_624982638 A-to-I Human chr17 - 43807248 43807248 43807248 TAAGGGGGAGGCTGGCATGGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCTGAGGCAGGC TAAGGGGGAGGCTGGCATGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGC T C MPP3 Ensembl:ENSG00000161647 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1339788380 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99276,RMVar_hsa_circ_184611 50670 RMVar_ID_50670 Human_SNP_ID_624982810 A-to-I Human chr17 - 43808083 43808083 43808083 ACTTTTTATTTTATTATTATTTTTTTAAAGACAGGGACTCACTATGTTGTCCAGGCTGGTCTTGA ACTTTTTATTTTATTATTATTTTTTTAAAGACTGGGACTCACTATGTTGTCCAGGCTGGTCTTGA T A MPP3 Ensembl:ENSG00000161647 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1015941925 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2507831,Human_RBP_ID_6597940,Human_RBP_ID_13018332 RMVar_hsa_circ_99276,RMVar_hsa_circ_184611 50671 RMVar_ID_50671 Human_SNP_ID_624985064 A-to-I Human chr17 - 43817418 43817418 43817418 GTTTAAGTGGGTGTCCTGCATTTTATCTGGCAACTCTACACCGTGTAGCACTTTACACTTTAGAA GTTTAAGTGGGTGTCCTGCATTTTATCTGGCACCTCTACACCGTGTAGCACTTTACACTTTAGAA T G MPP3 Ensembl:ENSG00000161647 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,cerebellum - 29129909,30559470 RNA-Seq:(High) rs1185252408 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13018463,Human_RBP_ID_17893117 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 50672 RMVar_ID_50672 Human_SNP_ID_624985691 A-to-I Human chr17 - 43820084 43820084 43820084 AAAATTAGCTGGGCATGGTTGCACACACCTGTAGTCCCAGCTACTCGGGAGGCTGGGGTGGGAGG AAAATTAGCTGGGCATGGTTGCACACACCTGTGGTCCCAGCTACTCGGGAGGCTGGGGTGGGAGG T C MPP3 Ensembl:ENSG00000161647 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1255873765 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25821,RMVar_hsa_circ_27266,RMVar_hsa_circ_184615,RMVar_hsa_circ_296486,RMVar_hsa_circ_29099,RMVar_hsa_circ_297972,RMVar_hsa_circ_184617 50673 RMVar_ID_50673 Human_SNP_ID_625034828 A-to-I Human chr17 - 44011432 44011432 44011432 CAGGCCCAGGAAGGGCACAGGGGCTGAGCACTACAGAAGTCACATGGGTTCTCAGGGTATGCCAG CAGGCCCAGGAAGGGCACAGGGGCTGAGCACTGCAGAAGTCACATGGGTTCTCAGGGTATGCCAG T C TMEM101 Ensembl:ENSG00000091947 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs897539156 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_490609,Human_RBP_ID_764528,Human_RBP_ID_1008408,Human_RBP_ID_5115165,Human_RBP_ID_5143237,Human_RBP_ID_6598075,Human_RBP_ID_9289154,Human_RBP_ID_13019048,Human_RBP_ID_17654756,Human_RBP_ID_17893164,Human_RBP_ID_23209996,Human_RBP_ID_23728141,Human_RBP_ID_26451635 Human_miRNA_ID_291827,Human_miRNA_ID_1973690,Human_miRNA_ID_1975868,Human_miRNA_ID_2376904,Human_miRNA_ID_2928244,Human_miRNA_ID_3032551 RMVar_hsa_circ_120198,RMVar_hsa_circ_184622 50674 RMVar_ID_50674 Human_SNP_ID_625034905 A-to-I Human chr17 - 44011916 44011916 44011916 ATCCTGGCCACTGATGGCTGAGTTTTATGGCAAGAGGCTGAGATGGGCACAGGGAGCCACTGAGG ATCCTGGCCACTGATGGCTGAGTTTTATGGCAGGAGGCTGAGATGGGCACAGGGAGCCACTGAGG T C TMEM101 Ensembl:ENSG00000091947 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs748317469 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_490629,Human_RBP_ID_1008410,Human_RBP_ID_6598094,Human_RBP_ID_9072248,Human_RBP_ID_13019068,Human_RBP_ID_17893167,Human_RBP_ID_22444660,Human_RBP_ID_23728153,Human_RBP_ID_27665548 RMVar_hsa_circ_120198,RMVar_hsa_circ_184622 50675 RMVar_ID_50675 Human_SNP_ID_625038944 A-to-I Human chr17 - 44026331 44026331 44026331 ACGCCTGTAAATCCCAGCACTTTGGGAGGTTGAGGTGGGAGGATCGCTTGAGTCCAGGAGTTGGA ACGCCTGTAAATCCCAGCACTTTGGGAGGTTGTGGTGGGAGGATCGCTTGAGTCCAGGAGTTGGA T A lnc-TMEM101-1 RNACentral:URS00008BC685 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1366275159 Functional Loss SNV dbSNP153 33..33 33 - - - 50676 RMVar_ID_50676 Human_SNP_ID_625039081 A-to-I Human chr17 - 44026932 44026932 44026932 TTTTTTTAAGACAAGGTCTCCCTCTGTCACCCAGGCTGGAGTGCTGTGGTGTGATCACAGCTTAC TTTTTTTAAGACAAGGTCTCCCTCTGTCACCCGGGCTGGAGTGCTGTGGTGTGATCACAGCTTAC T C lnc-TMEM101-1 RNACentral:URS00008BC685 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1219758345 Functional Loss SNV dbSNP153 33..33 33 - - - 50677 RMVar_ID_50677 Human_SNP_ID_625040771 A-to-I Human chr17 - 44033591 44033591 44033591 AGGCAGGAGCTCAAGACCATTCTGGGTGGCATAGTGAGACCCCCCATCTCTACAGAAAATACGTT AGGCAGGAGCTCAAGACCATTCTGGGTGGCATGGTGAGACCCCCCATCTCTACAGAAAATACGTT T C lnc-TMEM101-1 RNACentral:URS00008BC685 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1173798012 Functional Loss SNV dbSNP153 33..33 33 - - - 50678 RMVar_ID_50678 Human_SNP_ID_625041922 A-to-I Human chr17 - 44038294 44038294 44038294 TTGGGAGTGCAGTGGTGCGATTTTAGCTTACTATAGCCTCAATCTCCCCGGCTCTGGTGATTCTC TTGGGAGTGCAGTGGTGCGATTTTAGCTTACTGTAGCCTCAATCTCCCCGGCTCTGGTGATTCTC T C LSM12 Ensembl:ENSG00000161654 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1567954623 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50638 50679 RMVar_ID_50679 Human_SNP_ID_625042022 A-to-I Human chr17 - 44038511 44038511 44038511 AACTGGGACTACAGGCGCGCAGTCCCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGACAGTTT AACTGGGACTACAGGCGCGCAGTCCCACGCCCGGCTAATTTTTGTATTTTTAGTAGAGACAGTTT T C LSM12 Ensembl:ENSG00000161654 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1413046715 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50638 50680 RMVar_ID_50680 Human_SNP_ID_625042055 A-to-I Human chr17 - 44038608 44038608 44038608 ACTCTGTCACCAGGCTGGAGTCCAATGGTGCAATCTTGGCTCACTGCAATCTCTGCCTCCCAGGT ACTCTGTCACCAGGCTGGAGTCCAATGGTGCAGTCTTGGCTCACTGCAATCTCTGCCTCCCAGGT T C LSM12 Ensembl:ENSG00000161654 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs755595477 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_50638 50681 RMVar_ID_50681 Human_SNP_ID_625043259 A-to-I Human chr17 - 44042240 44042240 44042240 CTCTGTCGCCCAGGCTGGAGTGTAGTGGTACAATCTCGGCTCACTGCAGTCTCTGCCTCCCGTGT CTCTGTCGCCCAGGCTGGAGTGTAGTGGTACAGTCTCGGCTCACTGCAGTCTCTGCCTCCCGTGT T C LSM12 Ensembl:ENSG00000161654 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1050724209 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_184623,RMVar_hsa_circ_103845,RMVar_hsa_circ_351296 50682 RMVar_ID_50682 Human_SNP_ID_625044178 A-to-I Human chr17 - 44045625 44045625 44045625 TGGAGGTTGCAGTGGGCTGAGATTGTGCCATTACATTCCAGCCTGGGTGATAGAGTGAGACTCTG TGGAGGTTGCAGTGGGCTGAGATTGTGCCATTGCATTCCAGCCTGGGTGATAGAGTGAGACTCTG T C LSM12 Ensembl:ENSG00000161654 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs961257704 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13019884,Human_RBP_ID_17566489,Human_RBP_ID_25342476 RMVar_hsa_circ_184623,RMVar_hsa_circ_103845,RMVar_hsa_circ_351296 50683 RMVar_ID_50683 Human_SNP_ID_625044196 A-to-I Human chr17 - 44045691 44045691 44045691 TGGTGTGCTTCTGTGGTCCCAGCTACTTGGGAAGCTGAAGTGGGAGGATTGCTTGAGCCCAGTGG TGGTGTGCTTCTGTGGTCCCAGCTACTTGGGACGCTGAAGTGGGAGGATTGCTTGAGCCCAGTGG T G LSM12 Ensembl:ENSG00000161654 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1329328902 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17566489,Human_RBP_ID_25287121 RMVar_hsa_circ_184623,RMVar_hsa_circ_103845,RMVar_hsa_circ_351296 50684 RMVar_ID_50684 Human_SNP_ID_625045039 A-to-I Human chr17 - 44048299 44048299 44048299 TTTTGTAATTTTTGTAGAGATGGGGTTTCGCTATGTTGACCAGGCTGGTTTCGAACTCCTGGGCT TTTTGTAATTTTTGTAGAGATGGGGTTTCGCTGTGTTGACCAGGCTGGTTTCGAACTCCTGGGCT T C LSM12 Ensembl:ENSG00000161654 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1325900713 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_184623,RMVar_hsa_circ_103845,RMVar_hsa_circ_351296 50685 RMVar_ID_50685 Human_SNP_ID_625045070 A-to-I Human chr17 - 44048395 44048395 44048395 TAACTGAAACCTCCGCCTCCCGGGTTCAAGCAATTCCTCTGCCTCAGCCTCCCAAGTAGATGGGA TAACTGAAACCTCCGCCTCCCGGGTTCAAGCAGTTCCTCTGCCTCAGCCTCCCAAGTAGATGGGA T C LSM12 Ensembl:ENSG00000161654 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs891905759 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_184623,RMVar_hsa_circ_103845,RMVar_hsa_circ_351296 50686 RMVar_ID_50686 Human_SNP_ID_625045322 A-to-I Human chr17 - 44049370 44049370 44049370 TGTAGGCTGAGGTGGGAAGATCGCTTGAGCCCAGGAGTTTGTGACTGCATTGTGTAGGATCATGG TGTAGGCTGAGGTGGGAAGATCGCTTGAGCCCGGGAGTTTGTGACTGCATTGTGTAGGATCATGG T C LSM12 Ensembl:ENSG00000161654 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs570994499 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13019963 RMVar_hsa_circ_184623,RMVar_hsa_circ_103845,RMVar_hsa_circ_351296 50687 RMVar_ID_50687 Human_SNP_ID_625045337 A-to-I Human chr17 - 44049418 44049418 44049418 AAAAAAGTAGCTGGGTGTGGTGGCGCACACCTATAGTCTCAGCTACTCTGTAGGCTGAGGTGGGA AAAAAAGTAGCTGGGTGTGGTGGCGCACACCTGTAGTCTCAGCTACTCTGTAGGCTGAGGTGGGA T C LSM12 Ensembl:ENSG00000161654 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs537115117 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_184623,RMVar_hsa_circ_103845,RMVar_hsa_circ_351296 50688 RMVar_ID_50688 Human_SNP_ID_625045720 A-to-I Human chr17 - 44050878 44050878 44050878 TCCACCCGCCTATCTCCCAAAGTGCTGGAGTTACAGTTGTGAGCTACCATGCCTGTCCAGGAACA TCCACCCGCCTATCTCCCAAAGTGCTGGAGTTGCAGTTGTGAGCTACCATGCCTGTCCAGGAACA T C LSM12 Ensembl:ENSG00000161654 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1375078495 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_184623,RMVar_hsa_circ_103845,RMVar_hsa_circ_351296 50689 RMVar_ID_50689 Human_SNP_ID_625045931 A-to-I Human chr17 - 44051515 44051515 44051515 AGGGTCTTACTTTGTCACTTAGGTTGAAGTGCAGTGGTGCAATCTCACCTCACTGCCACCTCCTC AGGGTCTTACTTTGTCACTTAGGTTGAAGTGCTGTGGTGCAATCTCACCTCACTGCCACCTCCTC T A LSM12 Ensembl:ENSG00000161654 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs951850925 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13020038 RMVar_hsa_circ_184623,RMVar_hsa_circ_103845,RMVar_hsa_circ_351296 50690 RMVar_ID_50690 Human_SNP_ID_625045940 A-to-I Human chr17 - 44051547 44051547 44051547 TATATATATATATATTTCCCCCTCCCCGAGATAGGGTCTTACTTTGTCACTTAGGTTGAAGTGCA TATATATATATATATTTCCCCCTCCCCGAGATGGGGTCTTACTTTGTCACTTAGGTTGAAGTGCA T C LSM12 Ensembl:ENSG00000161654 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs961670061 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_184623,RMVar_hsa_circ_103845,RMVar_hsa_circ_351296 50691 RMVar_ID_50691 Human_SNP_ID_625046048 A-to-I Human chr17 - 44052021 44052021 44052021 TCATTGCTACCTCCGCCTCCCCGGTTCAAACAATTCTCCTGCCTCAGCCTCCCAGGTAGCTGGGA TCATTGCTACCTCCGCCTCCCCGGTTCAAACAGTTCTCCTGCCTCAGCCTCCCAGGTAGCTGGGA T C LSM12 Ensembl:ENSG00000161654 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs935265692 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_184623,RMVar_hsa_circ_103845,RMVar_hsa_circ_351296 50692 RMVar_ID_50692 Human_SNP_ID_625046069 A-to-I Human chr17 - 44052067 44052067 44052067 GAGTCTTGCTGTCACCCAGGCTGGAGTGCAGTAGCATGATCTTGGCTCATTGCTACCTCCGCCTC GAGTCTTGCTGTCACCCAGGCTGGAGTGCAGTGGCATGATCTTGGCTCATTGCTACCTCCGCCTC T C LSM12 Ensembl:ENSG00000161654 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs889829288 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_184623,RMVar_hsa_circ_103845,RMVar_hsa_circ_351296 50693 RMVar_ID_50693 Human_SNP_ID_625046958 A-to-I Human chr17 - 44055595 44055593 44055595 TCTGCTCACTGCAACCTCTACCTCCTGTGCTAAAGTAATTCTCTTGCCTCAGCCTCCTGAGTAGC TCTGCTCACTGCAACCTCTACCTCCTGTGCTA__GTAATTCTCTTGCCTCAGCCTCCTGAGTAGC CTT C LSM12 Ensembl:ENSG00000161654 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1309082413 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_184623,RMVar_hsa_circ_103845,RMVar_hsa_circ_351296 50694 RMVar_ID_50694 Human_SNP_ID_625046959 A-to-I Human chr17 - 44055595 44055595 44055595 TCTGCTCACTGCAACCTCTACCTCCTGTGCTAAAGTAATTCTCTTGCCTCAGCCTCCTGAGTAGC TCTGCTCACTGCAACCTCTACCTCCTGTGCTATAGTAATTCTCTTGCCTCAGCCTCCTGAGTAGC T A LSM12 Ensembl:ENSG00000161654 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs975360305 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_184623,RMVar_hsa_circ_103845,RMVar_hsa_circ_351296 50695 RMVar_ID_50695 Human_SNP_ID_625048006 A-to-I Human chr17 - 44058888 44058888 44058888 CTCAAGTGATCTTTCCACCTCGCCTCCCAAGTAGCTGGGACTACCGGCACAAACCACCACACCTG CTCAAGTGATCTTTCCACCTCGCCTCCCAAGTGGCTGGGACTACCGGCACAAACCACCACACCTG T C LSM12 Ensembl:ENSG00000161654 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs746397939 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23169586 RMVar_hsa_circ_184623,RMVar_hsa_circ_103845,RMVar_hsa_circ_351296 50696 RMVar_ID_50696 Human_SNP_ID_625052681 A-to-I Human chr17 - 44074740 44074738 44074740 ACCTGCGGGCCCGAGTGGCCACCTGCGAAGACAGGGCCGTCATTATGGGCCAGAGGGCTGCTCCT ACCTGCGGGCCCGAGTGGCCACCTGCGAAGAC__GGCCGTCATTATGGGCCAGAGGGCTGCTCCT CCT C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1268653937 Functional Loss DEL dbSNP153 33..34 33 - - - 50697 RMVar_ID_50697 Human_SNP_ID_625052682 A-to-I Human chr17 - 44074740 44074740 44074740 ACCTGCGGGCCCGAGTGGCCACCTGCGAAGACAGGGCCGTCATTATGGGCCAGAGGGCTGCTCCT ACCTGCGGGCCCGAGTGGCCACCTGCGAAGACGGGGCCGTCATTATGGGCCAGAGGGCTGCTCCT T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1280283104 Functional Loss SNV dbSNP153 33..33 33 - - - 50698 RMVar_ID_50698 Human_SNP_ID_625080420 A-to-I Human chr17 - 44173500 44173500 44173500 AGTAGAGACAAAAACCTCACTTACGTTGCCCAAACTATTCTCAAACTCCTGGACTCAAGCAATCC AGTAGAGACAAAAACCTCACTTACGTTGCCCAGACTATTCTCAAACTCCTGGACTCAAGCAATCC T C ASB16-AS1,ASB16-AS1:2 RNACentral:URS0000D599CE,RNACentral:URS0000D5C2D5 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs542998344 Functional Loss SNV dbSNP153 33..33 33 - - - 50699 RMVar_ID_50699 Human_SNP_ID_625080452 A-to-I Human chr17 - 44173645 44173645 44173645 AATTTTATTTTTTGTAGAGACAGGGTCTCACTATGTTTCCCAGTCTGGTCTTGAACTTCTGAGCT AATTTTATTTTTTGTAGAGACAGGGTCTCACTGTGTTTCCCAGTCTGGTCTTGAACTTCTGAGCT T C ASB16-AS1,ASB16-AS1:2 RNACentral:URS0000D599CE,RNACentral:URS0000D5C2D5 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1045527864 Functional Loss SNV dbSNP153 33..33 33 - - - 50700 RMVar_ID_50700 Human_SNP_ID_625080454 A-to-I Human chr17 - 44173656 44173654 44173656 CATGCCCGGCTAATTTTATTTTTTGTAGAGACAGGGTCTCACTATGTTTCCCAGTCTGGTCTTGA CATGCCCGGCTAATTTTATTTTTTGTAGAGAC__GGTCTCACTATGTTTCCCAGTCTGGTCTTGA CCT C ASB16-AS1,ASB16-AS1:2 RNACentral:URS0000D599CE,RNACentral:URS0000D5C2D5 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1022938918 Functional Loss DEL dbSNP153 33..34 33 - - - 50701 RMVar_ID_50701 Human_SNP_ID_625080481 A-to-I Human chr17 - 44173749 44173749 44173749 AGTACAGTGGCAGCATGATCATAGCTCACTGAAGCCTAGACCTCTTGGGCTCAAATGCTTTTCCT AGTACAGTGGCAGCATGATCATAGCTCACTGAGGCCTAGACCTCTTGGGCTCAAATGCTTTTCCT T C ASB16-AS1,ASB16-AS1:2 RNACentral:URS0000D599CE,RNACentral:URS0000D5C2D5 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1275255608 Functional Loss SNV dbSNP153 33..33 33 - - - 50702 RMVar_ID_50702 Human_SNP_ID_625082172 A-to-I Human chr17 - 44178565 44178565 44178565 GGAAGTTTGGGGCACAAGAATCGCTTGAACCTAGGTGGTAGAAGTTGCAGTGAGCCGAGATAGCG GGAAGTTTGGGGCACAAGAATCGCTTGAACCTTGGTGGTAGAAGTTGCAGTGAGCCGAGATAGCG T A ASB16-AS1 Ensembl:ENSG00000267080 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1203501527 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5248162 RMVar_hsa_circ_96797,RMVar_hsa_circ_184650 50703 RMVar_ID_50703 Human_SNP_ID_625082189 A-to-I Human chr17 - 44178611 44178611 44178611 AAAATCAGCCAGGTGTGGTGACTCATGCCTGTAGTCCCAGCTACTCGGAAGTTTGGGGCACAAGA AAAATCAGCCAGGTGTGGTGACTCATGCCTGTGGTCCCAGCTACTCGGAAGTTTGGGGCACAAGA T C ASB16-AS1 Ensembl:ENSG00000267080 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1023829948 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5248162 RMVar_hsa_circ_96797,RMVar_hsa_circ_184650 50704 RMVar_ID_50704 Human_SNP_ID_625082202 A-to-I Human chr17 + 44178661 44178661 44178661 CACCTGGCTGATTTTGTATTTTTAGTAGAGACAGGGTCTCACCATGTTGGCCAGGCTGGTCTCAC CACCTGGCTGATTTTGTATTTTTAGTAGAGACGGGGTCTCACCATGTTGGCCAGGCTGGTCTCAC A G ASB16 Ensembl:ENSG00000161664 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1007654432 Functional Loss SNV dbSNP153 33..33 33 - - - 50705 RMVar_ID_50705 Human_SNP_ID_625082337 A-to-I Human chr17 - 44179278 44179278 44179278 AAACTCCTGACCTCAGGTGATCCTCCCGCCTCAGTCTCCCAAAGTGCTGGGATTACAGGTGTAAG AAACTCCTGACCTCAGGTGATCCTCCCGCCTCGGTCTCCCAAAGTGCTGGGATTACAGGTGTAAG T C ASB16-AS1 Ensembl:ENSG00000267080 lincRNA intron GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line - 24183664,31158229 RNA-Seq:(High) rs1169112911 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96797,RMVar_hsa_circ_184650 50706 RMVar_ID_50706 Human_SNP_ID_625082362 A-to-I Human chr17 - 44179406 44179406 44179406 TGACCTCGTGATCCGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAACCACTGCGC TGACCTCGTGATCCGCCCACCTCGGCCTCCCAGAGTGCTGGGATTACAGGCATGAACCACTGCGC T C ASB16-AS1 Ensembl:ENSG00000267080 lincRNA intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1168681831 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96797,RMVar_hsa_circ_184650 50707 RMVar_ID_50707 Human_SNP_ID_625082402 A-to-I Human chr17 - 44179536 44179536 44179536 TCAAGTGATTCTCCTGCTTCAACCTCCTGAGTAGCTGAGATTACAGGCATCCGCCACTATGCCCG TCAAGTGATTCTCCTGCTTCAACCTCCTGAGTGGCTGAGATTACAGGCATCCGCCACTATGCCCG T C ASB16-AS1 Ensembl:ENSG00000267080 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1403985141 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_96797,RMVar_hsa_circ_184650 50708 RMVar_ID_50708 Human_SNP_ID_625083930 A-to-I Human chr17 - 44183950 44183950 44183950 GCCTCCCAGGTTCAAGTGATTCTCCTGCCTCAACCTACTGAATAGCTGGGAGTATATGTGTGTGC GCCTCCCAGGTTCAAGTGATTCTCCTGCCTCAGCCTACTGAATAGCTGGGAGTATATGTGTGTGC T C ASB16-AS1 Ensembl:ENSG00000267080 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs900597021 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99707,RMVar_hsa_circ_184652 50709 RMVar_ID_50709 Human_SNP_ID_625084108 A-to-I Human chr17 - 44184693 44184693 44184693 TCAAGATTGCAGAGAGCTGTGATCGCGCCACTATGCTCCAACCTGGGAGACAGAGTGAGACTCCG TCAAGATTGCAGAGAGCTGTGATCGCGCCACTGTGCTCCAACCTGGGAGACAGAGTGAGACTCCG T C ASB16-AS1 Ensembl:ENSG00000267080 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs370580025 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99707,RMVar_hsa_circ_184652 50710 RMVar_ID_50710 Human_SNP_ID_625084438 A-to-I Human chr17 - 44185934 44185934 44185934 GGGAGGCAGAGGTGGGAGGATCGCTTGAGCTCAGGAGTTCGAGGCTGCAGTGAGCTATGATCTGA GGGAGGCAGAGGTGGGAGGATCGCTTGAGCTCGGGAGTTCGAGGCTGCAGTGAGCTATGATCTGA T C ASB16-AS1 Ensembl:ENSG00000267080 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904612834 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6844 RMVar_hsa_circ_99707,RMVar_hsa_circ_184652 50711 RMVar_ID_50711 Human_SNP_ID_625084439 A-to-I Human chr17 - 44185934 44185934 44185934 GGGAGGCAGAGGTGGGAGGATCGCTTGAGCTCAGGAGTTCGAGGCTGCAGTGAGCTATGATCTGA GGGAGGCAGAGGTGGGAGGATCGCTTGAGCTCCGGAGTTCGAGGCTGCAGTGAGCTATGATCTGA T G ASB16-AS1 Ensembl:ENSG00000267080 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904612834 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6844 RMVar_hsa_circ_99707,RMVar_hsa_circ_184652 50712 RMVar_ID_50712 Human_SNP_ID_625084517 A-to-I Human chr17 - 44186171 44186171 44186171 GGATTACAGGCATGCGCCACCACGCCCCGCTAATTTTGTATTTTAGTAGAGACAGGGTTTCTCCA GGATTACAGGCATGCGCCACCACGCCCCGCTAGTTTTGTATTTTAGTAGAGACAGGGTTTCTCCA T C ASB16-AS1 Ensembl:ENSG00000267080 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1399860842 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99707,RMVar_hsa_circ_184652 50713 RMVar_ID_50713 Human_SNP_ID_625084523 A-to-I Human chr17 - 44186198 44186198 44186198 CTTTTGCCTCAGCCTGCCGAGTAGCTGGGATTACAGGCATGCGCCACCACGCCCCGCTAATTTTG CTTTTGCCTCAGCCTGCCGAGTAGCTGGGATTGCAGGCATGCGCCACCACGCCCCGCTAATTTTG T C ASB16-AS1 Ensembl:ENSG00000267080 lincRNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs374558371 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99707,RMVar_hsa_circ_184652 50714 RMVar_ID_50714 Human_SNP_ID_625084547 A-to-I Human chr17 - 44186258 44186258 44186258 GGAGTGCAATGGCGCGATCTCGGCTCACTGCAACCTCCGCCCCCCCGGGTTCAAGCGATTCTTTT GGAGTGCAATGGCGCGATCTCGGCTCACTGCAGCCTCCGCCCCCCCGGGTTCAAGCGATTCTTTT T C ASB16-AS1 Ensembl:ENSG00000267080 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1168587794 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99707,RMVar_hsa_circ_184652 50715 RMVar_ID_50715 Human_SNP_ID_625092128 A-to-I Human chr17 - 44208201 44208201 44208201 TACTCTGGAGGCTGAGTTGGAAGGATCACTTGAGCCTGGGAAGGTCAAGGCTGCAGTGAGCTGAG TACTCTGGAGGCTGAGTTGGAAGGATCACTTGCGCCTGGGAAGGTCAAGGCTGCAGTGAGCTGAG T G UBTF Ensembl:ENSG00000108312 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs942986432 Functional Loss SNV dbSNP153 33..33 33 - - - 50716 RMVar_ID_50716 Human_SNP_ID_625092397 A-to-I Human chr17 - 44209107 44209097 44209107 TGGAGTACAGTGGTGTAGTCTCGGCTCACTGCAACCTCCACCTCCCAGGTTCAAGCGATTCTCCT TGGAGTACAGTGGTGTAGTCTCGGCTCACTGC__________TCCCAGGTTCAAGCGATTCTCCT AGGTGGAGGTT A UBTF Ensembl:ENSG00000108312 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1555578387 Functional Loss DEL dbSNP153 33..42 33 - - - 50717 RMVar_ID_50717 Human_SNP_ID_625092402 A-to-I Human chr17 - 44209107 44209107 44209107 TGGAGTACAGTGGTGTAGTCTCGGCTCACTGCAACCTCCACCTCCCAGGTTCAAGCGATTCTCCT TGGAGTACAGTGGTGTAGTCTCGGCTCACTGCCACCTCCACCTCCCAGGTTCAAGCGATTCTCCT T G UBTF Ensembl:ENSG00000108312 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1348077107 Functional Loss SNV dbSNP153 33..33 33 - - - 50718 RMVar_ID_50718 Human_SNP_ID_625116283 A-to-I Human chr17 - 44291567 44291567 44291567 CCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGACCCACAGCGCCCAGCCTATATTGTATGAT CCTCAGCCTCCCAAAGTGCTGGGATTACAGGCCTGACCCACAGCGCCCAGCCTATATTGTATGAT T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs544029498 Functional Loss SNV dbSNP153 33..33 33 - - - 50719 RMVar_ID_50719 Human_SNP_ID_625118837 A-to-I Human chr17 - 44302159 44302159 44302159 AGGCATGGTGGCTTACACCTGTGGTCCCAGCTACTCAGGAAGCTGAGGTGGGAGGATCGCTTGAG AGGCATGGTGGCTTACACCTGTGGTCCCAGCTGCTCAGGAAGCTGAGGTGGGAGGATCGCTTGAG T C RUNDC3A-AS1 Ensembl:ENSG00000267750 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1358128869 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18699063 RMVar_hsa_circ_184671 50720 RMVar_ID_50720 Human_SNP_ID_625118986 A-to-I Human chr17 - 44302766 44302766 44302766 TGCAACCTCCACCTTCCAGATTCTCTTGCCTCAGCCTCCCAAGTAGCTGAGATTACAGGTGTGCA TGCAACCTCCACCTTCCAGATTCTCTTGCCTCGGCCTCCCAAGTAGCTGAGATTACAGGTGTGCA T C RUNDC3A-AS1 Ensembl:ENSG00000267750 lincRNA exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs150887367 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_184671 50721 RMVar_ID_50721 Human_SNP_ID_625125468 A-to-I Human chr17 - 44323752 44323752 44323752 CTGTAGTCCCAGCTACTTGGGAGGCTGAAGCAAGAGAACCGCTTGAACGGGGGTGGATGTTGCAG CTGTAGTCCCAGCTACTTGGGAGGCTGAAGCAGGAGAACCGCTTGAACGGGGGTGGATGTTGCAG T C SLC25A39 Ensembl:ENSG00000013306 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs945395984 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1825942,Human_Splice_Rec_1825988 RMVar_hsa_circ_93105,RMVar_hsa_circ_184681 50722 RMVar_ID_50722 Human_SNP_ID_625131720 A-to-I Human chr17 + 44346970 44346970 44346970 AAACCCCCATCTCTACTAAAAATACAAAAATTAGCCAGGTGTGGTAGCGCACACCTATAATCCCA AAACCCCCATCTCTACTAAAAATACAAAAATTGGCCAGGTGTGGTAGCGCACACCTATAATCCCA A G GRN Ensembl:ENSG00000030582 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs981708404 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99218,RMVar_hsa_circ_184685 50723 RMVar_ID_50723 Human_SNP_ID_625154523 A-to-I Human chr17 - 44427232 44427232 44427232 GTCTCTACGAAAAATACAAAAATTAGCCAGGCATAGTGGCATGCCCCTGTGGTCCTAGCAACTCA GTCTCTACGAAAAATACAAAAATTAGCCAGGCTTAGTGGCATGCCCCTGTGGTCCTAGCAACTCA T A GPATCH8 Ensembl:ENSG00000186566 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs558924826 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27509,RMVar_hsa_circ_324195,RMVar_hsa_circ_295765,RMVar_hsa_circ_184703,RMVar_hsa_circ_117027,RMVar_hsa_circ_281193,RMVar_hsa_circ_363952,RMVar_hsa_circ_184702,RMVar_hsa_circ_293048,RMVar_hsa_circ_275047,RMVar_hsa_circ_184705,RMVar_hsa_circ_184706,RMVar_hsa_circ_184704 50724 RMVar_ID_50724 Human_SNP_ID_625157491 A-to-I Human chr17 - 44438730 44438730 44438730 CCTACCCTAATGGTTTCTGCCTAACAAATGGTATTTCTTTTTTACAGCATTATGATCCTGGACTT CCTACCCTAATGGTTTCTGCCTAACAAATGGTTTTTCTTTTTTACAGCATTATGATCCTGGACTT T A GPATCH8 Ensembl:ENSG00000186566 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs9303361 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25287896 Human_Splice_Rec_1826443,Human_Splice_Rec_1826511,Human_Splice_Rec_1826525,Human_Splice_Rec_1826537 GWAS_ID_6594,GWAS_ID_6595,GWAS_ID_6596,GWAS_ID_6597,GWAS_ID_6598,GWAS_ID_6599,GWAS_ID_6600,GWAS_ID_6601 RMVar_hsa_circ_27509,RMVar_hsa_circ_295765,RMVar_hsa_circ_117027,RMVar_hsa_circ_184702,RMVar_hsa_circ_293048,RMVar_hsa_circ_275047,RMVar_hsa_circ_184705,RMVar_hsa_circ_184706,RMVar_hsa_circ_184704,RMVar_hsa_circ_184707,RMVar_hsa_circ_289900,RMVar_hsa_circ_319810,RMVar_hsa_circ_184708 50725 RMVar_ID_50725 Human_SNP_ID_625157492 A-to-I Human chr17 - 44438730 44438730 44438730 CCTACCCTAATGGTTTCTGCCTAACAAATGGTATTTCTTTTTTACAGCATTATGATCCTGGACTT CCTACCCTAATGGTTTCTGCCTAACAAATGGTGTTTCTTTTTTACAGCATTATGATCCTGGACTT T C GPATCH8 Ensembl:ENSG00000186566 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs9303361 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25287896 Human_Splice_Rec_1826443,Human_Splice_Rec_1826511,Human_Splice_Rec_1826525,Human_Splice_Rec_1826537 GWAS_ID_6594,GWAS_ID_6595,GWAS_ID_6596,GWAS_ID_6597,GWAS_ID_6598,GWAS_ID_6599,GWAS_ID_6600,GWAS_ID_6601 RMVar_hsa_circ_27509,RMVar_hsa_circ_295765,RMVar_hsa_circ_117027,RMVar_hsa_circ_184702,RMVar_hsa_circ_293048,RMVar_hsa_circ_275047,RMVar_hsa_circ_184705,RMVar_hsa_circ_184706,RMVar_hsa_circ_184704,RMVar_hsa_circ_184707,RMVar_hsa_circ_289900,RMVar_hsa_circ_319810,RMVar_hsa_circ_184708 50726 RMVar_ID_50726 Human_SNP_ID_625158026 A-to-I Human chr17 - 44441077 44441077 44441077 TTGGGAGGCCAAGGTGGCAGATCATGAGGTCAAGAGATCGAGACCATCCTGGCCAATATGGTGAA TTGGGAGGCCAAGGTGGCAGATCATGAGGTCAGGAGATCGAGACCATCCTGGCCAATATGGTGAA T C GPATCH8 Ensembl:ENSG00000186566 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1222241924 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27509,RMVar_hsa_circ_295765,RMVar_hsa_circ_117027,RMVar_hsa_circ_184702,RMVar_hsa_circ_293048,RMVar_hsa_circ_275047,RMVar_hsa_circ_184705,RMVar_hsa_circ_184706,RMVar_hsa_circ_184704,RMVar_hsa_circ_184707,RMVar_hsa_circ_289900,RMVar_hsa_circ_319810,RMVar_hsa_circ_184708 50727 RMVar_ID_50727 Human_SNP_ID_625158599 A-to-I Human chr17 - 44443052 44443052 44443052 CTCTTTTTCGACAAGGTTTTTCTCTGTCACCCAGGCTGGAGTGCAGTGGTGCGATGATAGCTCAC CTCTTTTTCGACAAGGTTTTTCTCTGTCACCCGGGCTGGAGTGCAGTGGTGCGATGATAGCTCAC T C GPATCH8 Ensembl:ENSG00000186566 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1040861024 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13231072 RMVar_hsa_circ_27509,RMVar_hsa_circ_295765,RMVar_hsa_circ_117027,RMVar_hsa_circ_184702,RMVar_hsa_circ_293048,RMVar_hsa_circ_275047,RMVar_hsa_circ_184705,RMVar_hsa_circ_184706,RMVar_hsa_circ_184704,RMVar_hsa_circ_184707,RMVar_hsa_circ_289900,RMVar_hsa_circ_319810,RMVar_hsa_circ_184708 50728 RMVar_ID_50728 Human_SNP_ID_625158761 A-to-I Human chr17 - 44443833 44443833 44443833 AAATCCCGTCTCTACAAAAAATAACAAGAATTAGCCACATGTGGTGGTGTGCACCTGTAGTCCCA AAATCCCGTCTCTACAAAAAATAACAAGAATTTGCCACATGTGGTGGTGTGCACCTGTAGTCCCA T A GPATCH8 Ensembl:ENSG00000186566 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1188724003 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27509,RMVar_hsa_circ_295765,RMVar_hsa_circ_117027,RMVar_hsa_circ_184702,RMVar_hsa_circ_293048,RMVar_hsa_circ_275047,RMVar_hsa_circ_184705,RMVar_hsa_circ_184706,RMVar_hsa_circ_184704,RMVar_hsa_circ_184707,RMVar_hsa_circ_289900,RMVar_hsa_circ_319810,RMVar_hsa_circ_184708 50729 RMVar_ID_50729 Human_SNP_ID_625158918 A-to-I Human chr17 - 44444552 44444552 44444552 GCCAGGCTGATCTCGACCTCCTGACCTCAAGTAGTCTGCCTGCCTTGGCCTCCCACAGTGCTGGG GCCAGGCTGATCTCGACCTCCTGACCTCAAGTCGTCTGCCTGCCTTGGCCTCCCACAGTGCTGGG T G GPATCH8 Ensembl:ENSG00000186566 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs913892465 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27509,RMVar_hsa_circ_295765,RMVar_hsa_circ_117027,RMVar_hsa_circ_184702,RMVar_hsa_circ_293048,RMVar_hsa_circ_275047,RMVar_hsa_circ_184705,RMVar_hsa_circ_184706,RMVar_hsa_circ_184704,RMVar_hsa_circ_184707,RMVar_hsa_circ_289900,RMVar_hsa_circ_319810,RMVar_hsa_circ_184708 50730 RMVar_ID_50730 Human_SNP_ID_625158927 A-to-I Human chr17 - 44444581 44444581 44444581 TTAAATGCAGACGAGGTTTTGCCATGTTGGCCAGGCTGATCTCGACCTCCTGACCTCAAGTAGTC TTAAATGCAGACGAGGTTTTGCCATGTTGGCCGGGCTGATCTCGACCTCCTGACCTCAAGTAGTC T C GPATCH8 Ensembl:ENSG00000186566 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs533345139 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27509,RMVar_hsa_circ_295765,RMVar_hsa_circ_117027,RMVar_hsa_circ_184702,RMVar_hsa_circ_293048,RMVar_hsa_circ_275047,RMVar_hsa_circ_184705,RMVar_hsa_circ_184706,RMVar_hsa_circ_184704,RMVar_hsa_circ_184707,RMVar_hsa_circ_289900,RMVar_hsa_circ_319810,RMVar_hsa_circ_184708 50731 RMVar_ID_50731 Human_SNP_ID_625159149 A-to-I Human chr17 - 44445540 44445539 44445541 GATCGCGCTGTTGCACTCCAGCCTAGGCAACAAGAGTGAAACTCCATCTTAGGGGGGGAAAAAAA GATCGCGCTGTTGCACTCCAGCCTAGGCAAC__GAGTGAAACTCCATCTTAGGGGGGGAAAAAAA CTT C GPATCH8 Ensembl:ENSG00000186566 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459481222 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_5185265 RMVar_hsa_circ_27509,RMVar_hsa_circ_295765,RMVar_hsa_circ_117027,RMVar_hsa_circ_184702,RMVar_hsa_circ_293048,RMVar_hsa_circ_275047,RMVar_hsa_circ_184705,RMVar_hsa_circ_184706,RMVar_hsa_circ_184704,RMVar_hsa_circ_184707,RMVar_hsa_circ_289900,RMVar_hsa_circ_319810,RMVar_hsa_circ_184708 50732 RMVar_ID_50732 Human_SNP_ID_625159362 A-to-I Human chr17 - 44446399 44446399 44446399 CACACGCCTGGCTAATTTTTTGTGTTTTTAGTAGAGACTGGGTTTCGCCGTGTTAGCCAGGATGG CACACGCCTGGCTAATTTTTTGTGTTTTTAGTGGAGACTGGGTTTCGCCGTGTTAGCCAGGATGG T C GPATCH8 Ensembl:ENSG00000186566 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1190160303 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27509,RMVar_hsa_circ_295765,RMVar_hsa_circ_117027,RMVar_hsa_circ_184702,RMVar_hsa_circ_293048,RMVar_hsa_circ_275047,RMVar_hsa_circ_184705,RMVar_hsa_circ_184706,RMVar_hsa_circ_184704,RMVar_hsa_circ_184707,RMVar_hsa_circ_289900,RMVar_hsa_circ_319810,RMVar_hsa_circ_184708 50733 RMVar_ID_50733 Human_SNP_ID_625160099 A-to-I Human chr17 - 44449040 44449040 44449040 AACTCCTAACCTAAGGTCATCCACCCGCCTCAACCTCCCAAAGTGCTGGGATTACAGGCGTGAGC AACTCCTAACCTAAGGTCATCCACCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGC T C GPATCH8 Ensembl:ENSG00000186566 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1403749949 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27509,RMVar_hsa_circ_295765,RMVar_hsa_circ_117027,RMVar_hsa_circ_184702,RMVar_hsa_circ_293048,RMVar_hsa_circ_275047,RMVar_hsa_circ_184705,RMVar_hsa_circ_184706,RMVar_hsa_circ_184704,RMVar_hsa_circ_184707,RMVar_hsa_circ_289900,RMVar_hsa_circ_319810,RMVar_hsa_circ_184708 50734 RMVar_ID_50734 Human_SNP_ID_625160100 A-to-I Human chr17 - 44449040 44449040 44449040 AACTCCTAACCTAAGGTCATCCACCCGCCTCAACCTCCCAAAGTGCTGGGATTACAGGCGTGAGC AACTCCTAACCTAAGGTCATCCACCCGCCTCACCCTCCCAAAGTGCTGGGATTACAGGCGTGAGC T G GPATCH8 Ensembl:ENSG00000186566 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1403749949 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27509,RMVar_hsa_circ_295765,RMVar_hsa_circ_117027,RMVar_hsa_circ_184702,RMVar_hsa_circ_293048,RMVar_hsa_circ_275047,RMVar_hsa_circ_184705,RMVar_hsa_circ_184706,RMVar_hsa_circ_184704,RMVar_hsa_circ_184707,RMVar_hsa_circ_289900,RMVar_hsa_circ_319810,RMVar_hsa_circ_184708 50735 RMVar_ID_50735 Human_SNP_ID_625160113 A-to-I Human chr17 - 44449079 44449079 44449079 CAGAGACAGGGTTTCACCATGTTGGCCAGGCTAGTCTCGAACTCCTAACCTAAGGTCATCCACCC CAGAGACAGGGTTTCACCATGTTGGCCAGGCTTGTCTCGAACTCCTAACCTAAGGTCATCCACCC T A GPATCH8 Ensembl:ENSG00000186566 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1198456592 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27509,RMVar_hsa_circ_295765,RMVar_hsa_circ_117027,RMVar_hsa_circ_184702,RMVar_hsa_circ_293048,RMVar_hsa_circ_275047,RMVar_hsa_circ_184705,RMVar_hsa_circ_184706,RMVar_hsa_circ_184704,RMVar_hsa_circ_184707,RMVar_hsa_circ_289900,RMVar_hsa_circ_319810,RMVar_hsa_circ_184708 50736 RMVar_ID_50736 Human_SNP_ID_625160805 A-to-I Human chr17 - 44452088 44452088 44452088 TCCTGTATTTTTATTAGAGACGGGGTTTCACTATGTTGGCCAGACTGGTCTCAAACTCCTGACCT TCCTGTATTTTTATTAGAGACGGGGTTTCACTGTGTTGGCCAGACTGGTCTCAAACTCCTGACCT T C GPATCH8 Ensembl:ENSG00000186566 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1435809646 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25288051 RMVar_hsa_circ_27509,RMVar_hsa_circ_295765,RMVar_hsa_circ_117027,RMVar_hsa_circ_184702,RMVar_hsa_circ_293048,RMVar_hsa_circ_275047,RMVar_hsa_circ_184705,RMVar_hsa_circ_184706,RMVar_hsa_circ_184704,RMVar_hsa_circ_184707,RMVar_hsa_circ_289900,RMVar_hsa_circ_319810,RMVar_hsa_circ_184708 50737 RMVar_ID_50737 Human_SNP_ID_625160806 A-to-I Human chr17 - 44452088 44452088 44452088 TCCTGTATTTTTATTAGAGACGGGGTTTCACTATGTTGGCCAGACTGGTCTCAAACTCCTGACCT TCCTGTATTTTTATTAGAGACGGGGTTTCACTCTGTTGGCCAGACTGGTCTCAAACTCCTGACCT T G GPATCH8 Ensembl:ENSG00000186566 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1435809646 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25288051 RMVar_hsa_circ_27509,RMVar_hsa_circ_295765,RMVar_hsa_circ_117027,RMVar_hsa_circ_184702,RMVar_hsa_circ_293048,RMVar_hsa_circ_275047,RMVar_hsa_circ_184705,RMVar_hsa_circ_184706,RMVar_hsa_circ_184704,RMVar_hsa_circ_184707,RMVar_hsa_circ_289900,RMVar_hsa_circ_319810,RMVar_hsa_circ_184708 50738 RMVar_ID_50738 Human_SNP_ID_625161037 A-to-I Human chr17 - 44452966 44452966 44452966 AAAATTAGCTGGGCGTGATGGCATGTGCCTGTAGTCCCAGCCACCTGGGAGAATGAGGTGGGAGA AAAATTAGCTGGGCGTGATGGCATGTGCCTGTGGTCCCAGCCACCTGGGAGAATGAGGTGGGAGA T C GPATCH8 Ensembl:ENSG00000186566 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs980768007 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13024100 RMVar_hsa_circ_27509,RMVar_hsa_circ_295765,RMVar_hsa_circ_117027,RMVar_hsa_circ_184702,RMVar_hsa_circ_293048,RMVar_hsa_circ_275047,RMVar_hsa_circ_184705,RMVar_hsa_circ_184706,RMVar_hsa_circ_184704,RMVar_hsa_circ_184707,RMVar_hsa_circ_289900,RMVar_hsa_circ_319810,RMVar_hsa_circ_184708 50739 RMVar_ID_50739 Human_SNP_ID_625161048 A-to-I Human chr17 - 44452992 44452992 44452992 CCCATCTCTACTTAAAATGCAAAGAAAAAATTAGCTGGGCGTGATGGCATGTGCCTGTAGTCCCA CCCATCTCTACTTAAAATGCAAAGAAAAAATTCGCTGGGCGTGATGGCATGTGCCTGTAGTCCCA T G GPATCH8 Ensembl:ENSG00000186566 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1250244463 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27509,RMVar_hsa_circ_295765,RMVar_hsa_circ_117027,RMVar_hsa_circ_184702,RMVar_hsa_circ_293048,RMVar_hsa_circ_275047,RMVar_hsa_circ_184705,RMVar_hsa_circ_184706,RMVar_hsa_circ_184704,RMVar_hsa_circ_184707,RMVar_hsa_circ_289900,RMVar_hsa_circ_319810,RMVar_hsa_circ_184708 50740 RMVar_ID_50740 Human_SNP_ID_625162133 A-to-I Human chr17 - 44456901 44456901 44456901 CGAGATTGCGCCACTGCACTCCATCCTGGGCAACAGAGCGAGACTGTGTCTCAAAAAAAAAAAAT CGAGATTGCGCCACTGCACTCCATCCTGGGCAGCAGAGCGAGACTGTGTCTCAAAAAAAAAAAAT T C GPATCH8 Ensembl:ENSG00000186566 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1244485662 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27509,RMVar_hsa_circ_295765,RMVar_hsa_circ_117027,RMVar_hsa_circ_184702,RMVar_hsa_circ_293048,RMVar_hsa_circ_275047,RMVar_hsa_circ_184705,RMVar_hsa_circ_184706,RMVar_hsa_circ_184704,RMVar_hsa_circ_184707,RMVar_hsa_circ_289900,RMVar_hsa_circ_319810,RMVar_hsa_circ_184708 50741 RMVar_ID_50741 Human_SNP_ID_625162446 A-to-I Human chr17 - 44458168 44458168 44458168 TAGCTCACTGCAGCCTTGATCTCCTGGGCTCAAGTGATCCTCCTGCCTTAGACCCATGAGTAGTG TAGCTCACTGCAGCCTTGATCTCCTGGGCTCAGGTGATCCTCCTGCCTTAGACCCATGAGTAGTG T C GPATCH8 Ensembl:ENSG00000186566 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1026766631 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27509,RMVar_hsa_circ_295765,RMVar_hsa_circ_117027,RMVar_hsa_circ_184702,RMVar_hsa_circ_293048,RMVar_hsa_circ_275047,RMVar_hsa_circ_184705,RMVar_hsa_circ_184706,RMVar_hsa_circ_184704,RMVar_hsa_circ_184707,RMVar_hsa_circ_289900,RMVar_hsa_circ_319810,RMVar_hsa_circ_184708 50742 RMVar_ID_50742 Human_SNP_ID_625162572 A-to-I Human chr17 - 44458614 44458614 44458614 GGAAGGCTGAGGCAGGAGGATCCCTTGACTCCAGGAGTTCGAAGTTGCAGTGAGCTGTGATTGTG GGAAGGCTGAGGCAGGAGGATCCCTTGACTCCGGGAGTTCGAAGTTGCAGTGAGCTGTGATTGTG T C GPATCH8 Ensembl:ENSG00000186566 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1373521589 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27509,RMVar_hsa_circ_295765,RMVar_hsa_circ_117027,RMVar_hsa_circ_184702,RMVar_hsa_circ_293048,RMVar_hsa_circ_275047,RMVar_hsa_circ_184705,RMVar_hsa_circ_184706,RMVar_hsa_circ_184704,RMVar_hsa_circ_184707,RMVar_hsa_circ_289900,RMVar_hsa_circ_319810,RMVar_hsa_circ_184708 50743 RMVar_ID_50743 Human_SNP_ID_625162619 A-to-I Human chr17 - 44458750 44458749 44458750 GGAGGCCAAGGTGGGAAGATCACTTGAGGCCAAGGGTTCAAGACCAGCTTGGGCAACAACAAGAC GGAGGCCAAGGTGGGAAGATCACTTGAGGCCA_GGGTTCAAGACCAGCTTGGGCAACAACAAGAC CT C GPATCH8 Ensembl:ENSG00000186566 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs999816945 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_27509,RMVar_hsa_circ_295765,RMVar_hsa_circ_117027,RMVar_hsa_circ_184702,RMVar_hsa_circ_293048,RMVar_hsa_circ_275047,RMVar_hsa_circ_184705,RMVar_hsa_circ_184706,RMVar_hsa_circ_184704,RMVar_hsa_circ_184707,RMVar_hsa_circ_289900,RMVar_hsa_circ_319810,RMVar_hsa_circ_184708 50744 RMVar_ID_50744 Human_SNP_ID_625163602 A-to-I Human chr17 - 44463209 44463209 44463209 AAGTGTGTTGAGAGGAACACAAGGACAGGTGCAGTGGCTCATGTCTGTAATCCCAGCAGTTTGGG AAGTGTGTTGAGAGGAACACAAGGACAGGTGCGGTGGCTCATGTCTGTAATCCCAGCAGTTTGGG T C GPATCH8 Ensembl:ENSG00000186566 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1251643198 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13024388 RMVar_hsa_circ_27509,RMVar_hsa_circ_295765,RMVar_hsa_circ_117027,RMVar_hsa_circ_184702,RMVar_hsa_circ_293048,RMVar_hsa_circ_275047,RMVar_hsa_circ_184705,RMVar_hsa_circ_184706,RMVar_hsa_circ_184704,RMVar_hsa_circ_184707,RMVar_hsa_circ_289900,RMVar_hsa_circ_319810,RMVar_hsa_circ_184708 50745 RMVar_ID_50745 Human_SNP_ID_625163661 A-to-I Human chr17 - 44463455 44463455 44463455 TTGAACCTGGAAGGCGGAGGTTGCAGTGAGCCAAGATCGTGCACCTGTACTCCAGCCTGGGCAAC TTGAACCTGGAAGGCGGAGGTTGCAGTGAGCCGAGATCGTGCACCTGTACTCCAGCCTGGGCAAC T C GPATCH8 Ensembl:ENSG00000186566 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs961115520 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13024397,Human_RBP_ID_25342591 RMVar_hsa_circ_27509,RMVar_hsa_circ_295765,RMVar_hsa_circ_117027,RMVar_hsa_circ_184702,RMVar_hsa_circ_293048,RMVar_hsa_circ_275047,RMVar_hsa_circ_184705,RMVar_hsa_circ_184706,RMVar_hsa_circ_184704,RMVar_hsa_circ_184707,RMVar_hsa_circ_289900,RMVar_hsa_circ_319810,RMVar_hsa_circ_184708 50746 RMVar_ID_50746 Human_SNP_ID_625167161 A-to-I Human chr17 - 44478458 44478458 44478458 TATAGACAAGGTCTTGCTCGCTATGTTGCCCAAGTTGATGTCCAACTTCCTGGCCTCCAGCAGTG TATAGACAAGGTCTTGCTCGCTATGTTGCCCAGGTTGATGTCCAACTTCCTGGCCTCCAGCAGTG T C GPATCH8 Ensembl:ENSG00000186566 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1352281578 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90707,RMVar_hsa_circ_184710,RMVar_hsa_circ_184712 50747 RMVar_ID_50747 Human_SNP_ID_625170004 A-to-I Human chr17 - 44488996 44488996 44488996 GGAGTGCAATGGGGCAATCTTGGCTCACTGCAACCTCTGCCTCCCGGGTTCAAGCAGTTTGATTA GGAGTGCAATGGGGCAATCTTGGCTCACTGCAGCCTCTGCCTCCCGGGTTCAAGCAGTTTGATTA T C GPATCH8 Ensembl:ENSG00000186566 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444260949 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90707,RMVar_hsa_circ_184710,RMVar_hsa_circ_184712 50748 RMVar_ID_50748 Human_SNP_ID_625170103 A-to-I Human chr17 - 44489408 44489408 44489408 TGAACCCAGGAGGGGTAGGTTGCAGTGAGCCAAGATGGCACCATTGCATTCCAGCCTGGGTGACA TGAACCCAGGAGGGGTAGGTTGCAGTGAGCCACGATGGCACCATTGCATTCCAGCCTGGGTGACA T G GPATCH8 Ensembl:ENSG00000186566 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1199305143 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90707,RMVar_hsa_circ_184710,RMVar_hsa_circ_184712 50749 RMVar_ID_50749 Human_SNP_ID_625170104 A-to-I Human chr17 - 44489409 44489409 44489409 TTGAACCCAGGAGGGGTAGGTTGCAGTGAGCCAAGATGGCACCATTGCATTCCAGCCTGGGTGAC TTGAACCCAGGAGGGGTAGGTTGCAGTGAGCCGAGATGGCACCATTGCATTCCAGCCTGGGTGAC T C GPATCH8 Ensembl:ENSG00000186566 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1186344715 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90707,RMVar_hsa_circ_184710,RMVar_hsa_circ_184712 50750 RMVar_ID_50750 Human_SNP_ID_625170107 A-to-I Human chr17 - 44489417 44489417 44489417 AGAATTGCTTGAACCCAGGAGGGGTAGGTTGCAGTGAGCCAAGATGGCACCATTGCATTCCAGCC AGAATTGCTTGAACCCAGGAGGGGTAGGTTGCGGTGAGCCAAGATGGCACCATTGCATTCCAGCC T C GPATCH8 Ensembl:ENSG00000186566 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1163725041 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90707,RMVar_hsa_circ_184710,RMVar_hsa_circ_184712 50751 RMVar_ID_50751 Human_SNP_ID_625170578 A-to-I Human chr17 - 44491442 44491442 44491442 CGCTCTGTCACCAGGCTGGAGTGCAGTGGCGCAATCTCGGCTCACTGCAGTCTCTGCCTCCCAGA CGCTCTGTCACCAGGCTGGAGTGCAGTGGCGCGATCTCGGCTCACTGCAGTCTCTGCCTCCCAGA T C GPATCH8 Ensembl:ENSG00000186566 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232890635 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90707,RMVar_hsa_circ_184710,RMVar_hsa_circ_184712 50752 RMVar_ID_50752 Human_SNP_ID_625216977 A-to-I Human chr17 - 44670224 44670224 44670224 AGATCTTGCTCTGTTCCCCAGGTTGGAATGCAATGGTGTGGTTATGGCTCACTGTAGCCCTGACA AGATCTTGCTCTGTTCCCCAGGTTGGAATGCAGTGGTGTGGTTATGGCTCACTGTAGCCCTGACA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs992166908 Functional Loss SNV dbSNP153 33..33 33 - - - 50753 RMVar_ID_50753 Human_SNP_ID_625226859 A-to-I Human chr17 + 44712621 44712621 44712621 CCACCACGCCCAGCCAAATTTTTTGTATTTTTAGTAGAGATGGGGTTTTACCATGTTAGCCAGGA CCACCACGCCCAGCCAAATTTTTTGTATTTTTGGTAGAGATGGGGTTTTACCATGTTAGCCAGGA A G DBF4B Ensembl:ENSG00000161692 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1462652021 Functional Loss SNV dbSNP153 33..33 33 - - - 50754 RMVar_ID_50754 Human_SNP_ID_625226882 A-to-I Human chr17 + 44712700 44712700 44712700 TGACCTCACGATCTGCCCTCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCACAC TGACCTCACGATCTGCCCTCCTCAGCCTCCCAGAGTGCTGGGATTACAGGTGTGAGCCACCACAC A G DBF4B Ensembl:ENSG00000161692 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs923843186 Functional Loss SNV dbSNP153 33..33 33 - - - 50755 RMVar_ID_50755 Human_SNP_ID_625229533 A-to-I Human chr17 + 44723520 44723520 44723520 TCACACCTGTAATCCCAGCACTCTGGGAGGCCAAGGCAGGTGGATTACTTGACGTCAGGAGTTAG TCACACCTGTAATCCCAGCACTCTGGGAGGCCGAGGCAGGTGGATTACTTGACGTCAGGAGTTAG A G DBF4B Ensembl:ENSG00000161692 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1276285750 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39835,RMVar_hsa_circ_44810 50756 RMVar_ID_50756 Human_SNP_ID_625229553 A-to-I Human chr17 + 44723579 44723579 44723579 AGTTAGGGACTAACTACCCTGGCCTAAATGACAAAACCCTGTCTCTACTAAAAATAATGAAAATT AGTTAGGGACTAACTACCCTGGCCTAAATGACGAAACCCTGTCTCTACTAAAAATAATGAAAATT A G DBF4B Ensembl:ENSG00000161692 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs547368709 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39835,RMVar_hsa_circ_44810 50757 RMVar_ID_50757 Human_SNP_ID_625229704 A-to-I Human chr17 + 44724290 44724290 44724290 ACAGTGGCACATGCCTGTAGTCTCCGTTACTCAGTAGGCTGAGGCATGAGACTCGCTTGAGCCCC ACAGTGGCACATGCCTGTAGTCTCCGTTACTCGGTAGGCTGAGGCATGAGACTCGCTTGAGCCCC A G DBF4B Ensembl:ENSG00000161692 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs747550402 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13026280 RMVar_hsa_circ_39835,RMVar_hsa_circ_44810 50758 RMVar_ID_50758 Human_SNP_ID_625229835 A-to-I Human chr17 + 44724798 44724798 44724798 GTCCAGGAGTTTGAGACCAGCCTGGGCAACATAGTGAGACCTCATCTCTACGAAAAATAAAATTA GTCCAGGAGTTTGAGACCAGCCTGGGCAACATGGTGAGACCTCATCTCTACGAAAAATAAAATTA A G DBF4B Ensembl:ENSG00000161692 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1320455939 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39835,RMVar_hsa_circ_44810 50759 RMVar_ID_50759 Human_SNP_ID_625230339 A-to-I Human chr17 + 44726530 44726530 44726530 GCAATCCCCCCACCTCAGCCTCCCAAAATGTTAGGATTACAGGCATGAGCCACAGCATCCAGCTG GCAATCCCCCCACCTCAGCCTCCCAAAATGTTGGGATTACAGGCATGAGCCACAGCATCCAGCTG A G DBF4B Ensembl:ENSG00000161692 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1419159732 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39835,RMVar_hsa_circ_44810 50760 RMVar_ID_50760 Human_SNP_ID_625231118 A-to-I Human chr17 + 44729474 44729474 44729474 TTGATCCTCCCACCTCAGCCTCCTACAGTGCTAGGATTACAGGTATCAGCCACCACACCTGGTCC TTGATCCTCCCACCTCAGCCTCCTACAGTGCTGGGATTACAGGTATCAGCCACCACACCTGGTCC A G DBF4B Ensembl:ENSG00000161692 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs940778795 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_39835,RMVar_hsa_circ_44810 50761 RMVar_ID_50761 Human_SNP_ID_625233795 A-to-I Human chr17 + 44739965 44739965 44739965 TTTTGTATTTTTTGTAGAGACGGGGTTTGGCCATGTTGGCCTGGCTGATCACAAACTGGCCTCAG TTTTGTATTTTTTGTAGAGACGGGGTTTGGCCGTGTTGGCCTGGCTGATCACAAACTGGCCTCAG A G DBF4B Ensembl:ENSG00000161692 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1008522717 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69280,RMVar_hsa_circ_325571,RMVar_hsa_circ_52453,RMVar_hsa_circ_306723,RMVar_hsa_circ_184720,RMVar_hsa_circ_184721,RMVar_hsa_circ_373596,RMVar_hsa_circ_30101 50762 RMVar_ID_50762 Human_SNP_ID_625247649 A-to-I Human chr17 - 44790948 44790948 44790948 ATTCCTGTAATCCCAGCTACTCGGGAGGCTGAAGCAGGAGGACTGCTTGAGCCCAGGAGGTCAGG ATTCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGGACTGCTTGAGCCCAGGAGGTCAGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1295283490 Functional Loss SNV dbSNP153 33..33 33 - - - 50763 RMVar_ID_50763 Human_SNP_ID_625248566 A-to-I Human chr17 - 44793367 44793367 44793367 CCACAGTTGATCCGCCTGCCTGGGCCTCTCAAAATCCTGGAATTACAGGCTTGAGCCACTGTACC CCACAGTTGATCCGCCTGCCTGGGCCTCTCAACATCCTGGAATTACAGGCTTGAGCCACTGTACC T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027474733 Functional Loss SNV dbSNP153 33..33 33 - - - 50764 RMVar_ID_50764 Human_SNP_ID_625249959 A-to-I Human chr17 - 44798922 44798922 44798922 AGGCGGAGGTTGCAGTGAGCTGAGATTGCACCACTGCACTCCAGCTTGGGTGATGGAGTGAGACT AGGCGGAGGTTGCAGTGAGCTGAGATTGCACCTCTGCACTCCAGCTTGGGTGATGGAGTGAGACT T A GJC1 Ensembl:ENSG00000182963 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1287636257 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9862323 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 50765 RMVar_ID_50765 Human_SNP_ID_625249963 A-to-I Human chr17 - 44798957 44798957 44798957 GCTGAGGCATGAGATGACAATCTCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCTGAGATTGCA GCTGAGGCATGAGATGACAATCTCTTGAACCCTGGAGGCGGAGGTTGCAGTGAGCTGAGATTGCA T A GJC1 Ensembl:ENSG00000182963 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11546866 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 50766 RMVar_ID_50766 Human_SNP_ID_625249977 A-to-I Human chr17 - 44799026 44799026 44799026 AACTGTCTCTACTAAAAATATAAAAATTAGGTATGGTGGCACGTGCCTGTACTTACAGCTACTTG AACTGTCTCTACTAAAAATATAAAAATTAGGTGTGGTGGCACGTGCCTGTACTTACAGCTACTTG T C GJC1 Ensembl:ENSG00000182963 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs11546869 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1008493,Human_RBP_ID_23729060,Human_RBP_ID_26642681,Human_RBP_ID_27453159 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 50767 RMVar_ID_50767 Human_SNP_ID_625249978 A-to-I Human chr17 - 44799030 44799030 44799030 GCAAAACTGTCTCTACTAAAAATATAAAAATTAGGTATGGTGGCACGTGCCTGTACTTACAGCTA GCAAAACTGTCTCTACTAAAAATATAAAAATTGGGTATGGTGGCACGTGCCTGTACTTACAGCTA T C GJC1 Ensembl:ENSG00000182963 Protein coding 3'UTR GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs151047627 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1008493,Human_RBP_ID_17375931,Human_RBP_ID_17893588,Human_RBP_ID_18292767,Human_RBP_ID_23729060,Human_RBP_ID_26642681,Human_RBP_ID_27453159 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 50768 RMVar_ID_50768 Human_SNP_ID_625249995 A-to-I Human chr17 - 44799096 44799096 44799096 ACTTTGGGAGGCCAAGGCAGGTGGATCACATGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACAT ACTTTGGGAGGCCAAGGCAGGTGGATCACATGGGGTCAGGAGTTCGAGACCAGCCTGGCCAACAT T C GJC1 Ensembl:ENSG00000182963 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs11546867 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 50769 RMVar_ID_50769 Human_SNP_ID_625250043 A-to-I Human chr17 - 44799263 44799263 44799263 AGGCAGAGGTTGCTGTGAGCCGAGATCGCGCCACTGCACTCCAGCCTGGGTGACAGAGTAAGACT AGGCAGAGGTTGCTGTGAGCCGAGATCGCGCCGCTGCACTCCAGCCTGGGTGACAGAGTAAGACT T C GJC1 Ensembl:ENSG00000182963 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs550945920 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 50770 RMVar_ID_50770 Human_SNP_ID_625250052 A-to-I Human chr17 - 44799291 44799291 44799291 TGAGGCATGAGATTTCCTTGAACCTGGAAGGCAGAGGTTGCTGTGAGCCGAGATCGCGCCACTGC TGAGGCATGAGATTTCCTTGAACCTGGAAGGCGGAGGTTGCTGTGAGCCGAGATCGCGCCACTGC T C GJC1 Ensembl:ENSG00000182963 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs1240516142 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6599816 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 50771 RMVar_ID_50771 Human_SNP_ID_625250065 A-to-I Human chr17 - 44799344 44799344 44799344 AAAATTAGCCGGGCATGGTGGTGCACACCTGTAATCCCAGCTACTCGGGATGTTGAGGCATGAGA AAAATTAGCCGGGCATGGTGGTGCACACCTGTGATCCCAGCTACTCGGGATGTTGAGGCATGAGA T C GJC1 Ensembl:ENSG00000182963 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,31158229,32596459 RNA-Seq:(High) rs1441871209 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 50772 RMVar_ID_50772 Human_SNP_ID_625250090 A-to-I Human chr17 - 44799423 44799423 44799423 GGTGGGTGGATCACTAGAGGTCAGGAGTTTGAAACAAGCCTGGCCAACATGGTAAAACCCCCTCT GGTGGGTGGATCACTAGAGGTCAGGAGTTTGAGACAAGCCTGGCCAACATGGTAAAACCCCCTCT T C GJC1 Ensembl:ENSG00000182963 Protein coding 3'UTR GSE38233;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 24183664,29796672,31158229,31158229 RNA-Seq:(High) rs1478576776 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 50773 RMVar_ID_50773 Human_SNP_ID_625250103 A-to-I Human chr17 - 44799479 44799479 44799479 GTTCTCGGCTGTGCATGGTGGCTAACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGTGG GTTCTCGGCTGTGCATGGTGGCTAACACCTGTGATCCCAGCACTTTGGGAGGCTGAGGTGGGTGG T C GJC1 Ensembl:ENSG00000182963 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1209841037 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 50774 RMVar_ID_50774 Human_SNP_ID_625250164 A-to-I Human chr17 - 44799697 44799697 44799697 CTAGACTGGTCTCAAACTCCTGGGCCCAAGCAATCCTCCCATCACAGCCTCCGAAGGTGCTGGGA CTAGACTGGTCTCAAACTCCTGGGCCCAAGCAGTCCTCCCATCACAGCCTCCGAAGGTGCTGGGA T C GJC1 Ensembl:ENSG00000182963 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs969911836 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23169723 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 50775 RMVar_ID_50775 Human_SNP_ID_625250175 A-to-I Human chr17 - 44799739 44799739 44799739 ATTTTTGTATTTTTTGTAGAGACAGAGCTCTCACTATGTTGCCTAGACTGGTCTCAAACTCCTGG ATTTTTGTATTTTTTGTAGAGACAGAGCTCTCGCTATGTTGCCTAGACTGGTCTCAAACTCCTGG T C GJC1 Ensembl:ENSG00000182963 Protein coding 3'UTR GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1165038281 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6599824,Human_RBP_ID_27453160 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 50776 RMVar_ID_50776 Human_SNP_ID_625250177 A-to-I Human chr17 - 44799748 44799748 44799748 ACCTGGCTAATTTTTGTATTTTTTGTAGAGACAGAGCTCTCACTATGTTGCCTAGACTGGTCTCA ACCTGGCTAATTTTTGTATTTTTTGTAGAGACGGAGCTCTCACTATGTTGCCTAGACTGGTCTCA T C GJC1 Ensembl:ENSG00000182963 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs971666409 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6599824,Human_RBP_ID_13026750 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 50777 RMVar_ID_50777 Human_SNP_ID_625250188 A-to-I Human chr17 - 44799795 44799795 44799795 CCCACTTCAGCCTCCCAAGTAGCTGGTCTGCAAGTGCTCACCACCACACCTGGCTAATTTTTGTA CCCACTTCAGCCTCCCAAGTAGCTGGTCTGCAGGTGCTCACCACCACACCTGGCTAATTTTTGTA T C GJC1 Ensembl:ENSG00000182963 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs1317898944 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_132087 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 50778 RMVar_ID_50778 Human_SNP_ID_625250189 A-to-I Human chr17 - 44799807 44799807 44799807 TCAAGCAGTCCTCCCACTTCAGCCTCCCAAGTAGCTGGTCTGCAAGTGCTCACCACCACACCTGG TCAAGCAGTCCTCCCACTTCAGCCTCCCAAGTGGCTGGTCTGCAAGTGCTCACCACCACACCTGG T C GJC1 Ensembl:ENSG00000182963 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1420583256 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 50779 RMVar_ID_50779 Human_SNP_ID_625250190 A-to-I Human chr17 - 44799810 44799810 44799810 GGCTCAAGCAGTCCTCCCACTTCAGCCTCCCAAGTAGCTGGTCTGCAAGTGCTCACCACCACACC GGCTCAAGCAGTCCTCCCACTTCAGCCTCCCAGGTAGCTGGTCTGCAAGTGCTCACCACCACACC T C GJC1 Ensembl:ENSG00000182963 Protein coding 3'UTR GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs988464598 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 50780 RMVar_ID_50780 Human_SNP_ID_625250205 A-to-I Human chr17 - 44799862 44799862 44799862 CAGGCTAGAGTGCAATGGCACAATCTCAACTCACTACAGCCTGGACCTCCTTGGCTCAAGCAGTC CAGGCTAGAGTGCAATGGCACAATCTCAACTCGCTACAGCCTGGACCTCCTTGGCTCAAGCAGTC T C GJC1 Ensembl:ENSG00000182963 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs988166274 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 50781 RMVar_ID_50781 Human_SNP_ID_625250208 A-to-I Human chr17 - 44799880 44799880 44799880 TGGGGTTTGTTTTGAGCCCAGGCTAGAGTGCAATGGCACAATCTCAACTCACTACAGCCTGGACC TGGGGTTTGTTTTGAGCCCAGGCTAGAGTGCAGTGGCACAATCTCAACTCACTACAGCCTGGACC T C GJC1 Ensembl:ENSG00000182963 Protein coding 3'UTR GSE38233;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,32596459,32596459 RNA-Seq:(High) rs773178888 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 50782 RMVar_ID_50782 Human_SNP_ID_625250317 A-to-I Human chr17 - 44800246 44800246 44800246 AAATTAGCCGGGCGTGGTGGTGGGTACCTGTAATCCCAGCTACTCAGGAGGCTGAGATGAGAATC AAATTAGCCGGGCGTGGTGGTGGGTACCTGTAGTCCCAGCTACTCAGGAGGCTGAGATGAGAATC T C GJC1 Ensembl:ENSG00000182963 Protein coding 3'UTR GSE38233;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line - 24183664,29796672,31158229 RNA-Seq:(High) rs1362375504 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 50783 RMVar_ID_50783 Human_SNP_ID_625250319 A-to-I Human chr17 - 44800253 44800253 44800253 ATACCAAAAATTAGCCGGGCGTGGTGGTGGGTACCTGTAATCCCAGCTACTCAGGAGGCTGAGAT ATACCAAAAATTAGCCGGGCGTGGTGGTGGGTTCCTGTAATCCCAGCTACTCAGGAGGCTGAGAT T A GJC1 Ensembl:ENSG00000182963 Protein coding 3'UTR GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,29796672,31158229,31158229,31158229 RNA-Seq:(High) rs1302846101 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 50784 RMVar_ID_50784 Human_SNP_ID_625250320 A-to-I Human chr17 - 44800253 44800253 44800253 ATACCAAAAATTAGCCGGGCGTGGTGGTGGGTACCTGTAATCCCAGCTACTCAGGAGGCTGAGAT ATACCAAAAATTAGCCGGGCGTGGTGGTGGGTGCCTGTAATCCCAGCTACTCAGGAGGCTGAGAT T C GJC1 Ensembl:ENSG00000182963 Protein coding 3'UTR GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,29796672,31158229,31158229,31158229 RNA-Seq:(High) rs1302846101 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 50785 RMVar_ID_50785 Human_SNP_ID_625250334 A-to-I Human chr17 - 44800276 44800275 44800276 GTGAAACCCCGTCTCTACTAAAAATACCAAAAATTAGCCGGGCGTGGTGGTGGGTACCTGTAATC GTGAAACCCCGTCTCTACTAAAAATACCAAAA_TTAGCCGGGCGTGGTGGTGGGTACCTGTAATC AT A GJC1 Ensembl:ENSG00000182963 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1261693587 Functional Loss DEL 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 50786 RMVar_ID_50786 Human_SNP_ID_625250371 A-to-I Human chr17 - 44800343 44800343 44800343 AGCACTTTGGGAGGCCAAGGTGGGCGAATCACAAGGTCAGGAGTTTGAGACCAGCCTGGCCAACA AGCACTTTGGGAGGCCAAGGTGGGCGAATCACTAGGTCAGGAGTTTGAGACCAGCCTGGCCAACA T A GJC1 Ensembl:ENSG00000182963 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs866246115 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 50787 RMVar_ID_50787 Human_SNP_ID_625250372 A-to-I Human chr17 - 44800343 44800343 44800343 AGCACTTTGGGAGGCCAAGGTGGGCGAATCACAAGGTCAGGAGTTTGAGACCAGCCTGGCCAACA AGCACTTTGGGAGGCCAAGGTGGGCGAATCACGAGGTCAGGAGTTTGAGACCAGCCTGGCCAACA T C GJC1 Ensembl:ENSG00000182963 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs866246115 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 50788 RMVar_ID_50788 Human_SNP_ID_625250379 A-to-I Human chr17 - 44800359 44800359 44800359 TCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGCGAATCACAAGGTCAGGAGTTTGAG TCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGCGAATCACAAGGTCAGGAGTTTGAG T C GJC1 Ensembl:ENSG00000182963 Protein coding 3'UTR GSE47997;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;Bronchiolar epithelium,BERP35T1 cell line - 23474544,31158229 RNA-Seq:(High) rs545445732 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 50789 RMVar_ID_50789 Human_SNP_ID_625250396 A-to-I Human chr17 - 44800403 44800403 44800403 AAACGCCTTTTTAAAAATCAAAGGTTTTGGCCAGGCATGGTGGCTCACGCCTGTAATCCCAGCAC AAACGCCTTTTTAAAAATCAAAGGTTTTGGCCGGGCATGGTGGCTCACGCCTGTAATCCCAGCAC T C GJC1 Ensembl:ENSG00000182963 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1238324676 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 50790 RMVar_ID_50790 Human_SNP_ID_625250723 A-to-I Human chr17 - 44801664 44801664 44801664 AGGAGGCAGAGGTTGCAGTGAGCTGAGATCATACCATTGCACTCCAGCCTGCAAGACAGAGTGAA AGGAGGCAGAGGTTGCAGTGAGCTGAGATCATGCCATTGCACTCCAGCCTGCAAGACAGAGTGAA T C GJC1 Ensembl:ENSG00000182963 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-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 50791 RMVar_ID_50791 Human_SNP_ID_625250743 A-to-I Human chr17 - 44801799 44801799 44801799 GGAGTTCAAGACCAGACTGGTCAACATGGTGAAACTCCATCTCTACTAAAAATACAGAAATTAGC GGAGTTCAAGACCAGACTGGTCAACATGGTGACACTCCATCTCTACTAAAAATACAGAAATTAGC T G GJC1 Ensembl:ENSG00000182963 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1386383540 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_132097 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 50792 RMVar_ID_50792 Human_SNP_ID_625250998 A-to-I Human chr17 - 44802875 44802875 44802875 CCTCAGCCTCTTGATTAGCTGGGACTACAGGCATGTGCCACCATACTCGGCTAATTCTGTTTTAA CCTCAGCCTCTTGATTAGCTGGGACTACAGGCGTGTGCCACCATACTCGGCTAATTCTGTTTTAA T C GJC1 Ensembl:ENSG00000182963 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs939979049 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26460639 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 50793 RMVar_ID_50793 Human_SNP_ID_625251009 A-to-I Human chr17 - 44802946 44802946 44802946 CAGGCTGGAGTGCAGCAGCATGATCTCAGCTCACTGCAGCCTCTGCCTCCCAGGCTCAAGCAATC CAGGCTGGAGTGCAGCAGCATGATCTCAGCTCGCTGCAGCCTCTGCCTCCCAGGCTCAAGCAATC T C GJC1 Ensembl:ENSG00000182963 Protein coding intron GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line - 29129909,29796672,31158229 RNA-Seq:(High) rs940099560 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 50794 RMVar_ID_50794 Human_SNP_ID_625251011 A-to-I Human chr17 - 44802959 44802959 44802959 TCCCTCTTTCACCCAGGCTGGAGTGCAGCAGCATGATCTCAGCTCACTGCAGCCTCTGCCTCCCA TCCCTCTTTCACCCAGGCTGGAGTGCAGCAGCGTGATCTCAGCTCACTGCAGCCTCTGCCTCCCA T C GJC1 Ensembl:ENSG00000182963 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1228560376 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 50795 RMVar_ID_50795 Human_SNP_ID_625260257 A-to-I Human chr17 + 44836838 44836838 44836838 AAACCCCGTCTCTACTAAAAATACAAAAAATTAGCCGGGCGTGGTGGCGGGCGCTTGTGGTCCCA AAACCCCGTCTCTACTAAAAATACAAAAAATTTGCCGGGCGTGGTGGCGGGCGCTTGTGGTCCCA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1370881798 Functional Loss SNV dbSNP153 33..33 33 - - - 50796 RMVar_ID_50796 Human_SNP_ID_625264100 A-to-I Human chr17 - 44851023 44851023 44851023 CAAGGAAAAGAGAGGAGCTTGGGCTCACAGAAAGAGAAGGGGATGAAACCCCAAGGGGCCCTATC CAAGGAAAAGAGAGGAGCTTGGGCTCACAGAAGGAGAAGGGGATGAAACCCCAAGGGGCCCTATC T C EFTUD2 Ensembl:ENSG00000108883 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1028383819 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_491177,Human_RBP_ID_764911,Human_RBP_ID_1859563,Human_RBP_ID_8818574,Human_RBP_ID_18699326,Human_RBP_ID_22215128 Human_miRNA_ID_3118732 RMVar_hsa_circ_77080,RMVar_hsa_circ_106253,RMVar_hsa_circ_184733,RMVar_hsa_circ_184734 50797 RMVar_ID_50797 Human_SNP_ID_625266328 A-to-I Human chr17 - 44859099 44859099 44859099 GGACTGTGTGATGCATGATTTGCGGAAGATGTACTCAGAGATAGACATCAAGGTACAGCAGTATC GGACTGTGTGATGCATGATTTGCGGAAGATGTGCTCAGAGATAGACATCAAGGTACAGCAGTATC T C EFTUD2 Ensembl:ENSG00000108883 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1204892519 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_47585,Human_RBP_ID_1534971,Human_RBP_ID_1859578,Human_RBP_ID_3524880,Human_RBP_ID_3950734,Human_RBP_ID_4431827,Human_RBP_ID_8454050,Human_RBP_ID_8818602,Human_RBP_ID_13027933,Human_RBP_ID_18991547,Human_RBP_ID_23729175,Human_RBP_ID_27665761 Human_Splice_Rec_1827054,Human_Splice_Rec_1827055,Human_Splice_Rec_1827076,Human_Splice_Rec_1827077,Human_Splice_Rec_1827128,Human_Splice_Rec_1827129,Human_Splice_Rec_1827162,Human_Splice_Rec_1827163,Human_Splice_Rec_1827214,Human_Splice_Rec_1827215,Human_Splice_Rec_1827233,Human_Splice_Rec_1827292,Human_Splice_Rec_1827293 RMVar_hsa_circ_184735,RMVar_hsa_circ_22704,RMVar_hsa_circ_107001,RMVar_hsa_circ_124097,RMVar_hsa_circ_28544,RMVar_hsa_circ_108244,RMVar_hsa_circ_184738,RMVar_hsa_circ_184740,RMVar_hsa_circ_99119,RMVar_hsa_circ_184741,RMVar_hsa_circ_184739,RMVar_hsa_circ_18533,RMVar_hsa_circ_48361,RMVar_hsa_circ_348364,RMVar_hsa_circ_184743,RMVar_hsa_circ_300180,RMVar_hsa_circ_184742,RMVar_hsa_circ_265863 50798 RMVar_ID_50798 Human_SNP_ID_625266808 A-to-I Human chr17 - 44860764 44860764 44860764 AAAAACCCCGTCTCTACAAAAATACAAAAATTAGTTGGGCATGTTAGTGTGTGCCTGTAGTCCCA AAAAACCCCGTCTCTACAAAAATACAAAAATTTGTTGGGCATGTTAGTGTGTGCCTGTAGTCCCA T A EFTUD2 Ensembl:ENSG00000108883 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1434986241 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_184735,RMVar_hsa_circ_22704,RMVar_hsa_circ_124097,RMVar_hsa_circ_108244,RMVar_hsa_circ_184740,RMVar_hsa_circ_99119,RMVar_hsa_circ_184741,RMVar_hsa_circ_184739,RMVar_hsa_circ_103149,RMVar_hsa_circ_18533,RMVar_hsa_circ_265863,RMVar_hsa_circ_113326,RMVar_hsa_circ_31587,RMVar_hsa_circ_184745,RMVar_hsa_circ_55864,RMVar_hsa_circ_184744 50799 RMVar_ID_50799 Human_SNP_ID_625268318 A-to-I Human chr17 - 44867007 44867007 44867007 AAACTCCTAGGTTTGAGCAATCCTCCCACCTCAGCCTCCTGAGAAGCTGGGACTGCAGGTGCAAG AAACTCCTAGGTTTGAGCAATCCTCCCACCTCGGCCTCCTGAGAAGCTGGGACTGCAGGTGCAAG T C EFTUD2 Ensembl:ENSG00000108883 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1380609242 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124097,RMVar_hsa_circ_108244,RMVar_hsa_circ_184740,RMVar_hsa_circ_184741,RMVar_hsa_circ_68804,RMVar_hsa_circ_103149,RMVar_hsa_circ_265863,RMVar_hsa_circ_113326,RMVar_hsa_circ_31587,RMVar_hsa_circ_184745,RMVar_hsa_circ_55864,RMVar_hsa_circ_184744,RMVar_hsa_circ_184746,RMVar_hsa_circ_283264,RMVar_hsa_circ_82598,RMVar_hsa_circ_31418 50800 RMVar_ID_50800 Human_SNP_ID_625268987 A-to-I Human chr17 - 44869518 44869518 44869518 AAAGTAGAGGATCACTTGAGGCCAGGAGTTCAAAACCAGCCTAGGCAACATGGCAAGACCTCGTC AAAGTAGAGGATCACTTGAGGCCAGGAGTTCAGAACCAGCCTAGGCAACATGGCAAGACCTCGTC T C EFTUD2 Ensembl:ENSG00000108883 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1212861614 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13028084,Human_RBP_ID_22586190 RMVar_hsa_circ_124097,RMVar_hsa_circ_108244,RMVar_hsa_circ_184740,RMVar_hsa_circ_184741,RMVar_hsa_circ_68804,RMVar_hsa_circ_103149,RMVar_hsa_circ_265863,RMVar_hsa_circ_113326,RMVar_hsa_circ_31587,RMVar_hsa_circ_184745,RMVar_hsa_circ_184744,RMVar_hsa_circ_184746,RMVar_hsa_circ_283264,RMVar_hsa_circ_82598,RMVar_hsa_circ_101650,RMVar_hsa_circ_367910,RMVar_hsa_circ_302184,RMVar_hsa_circ_184749,RMVar_hsa_circ_184750 50801 RMVar_ID_50801 Human_SNP_ID_625269967 A-to-I Human chr17 - 44873434 44873434 44873434 GGAGGATTGCGTGAGCTTGAGAGATCGAGGCTACAGTGAATGGTGATTGTACCACTGTGCTCCAG GGAGGATTGCGTGAGCTTGAGAGATCGAGGCTGCAGTGAATGGTGATTGTACCACTGTGCTCCAG T C EFTUD2 Ensembl:ENSG00000108883 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs575956930 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_235979,Human_RBP_ID_13028206,Human_RBP_ID_17565955,Human_RBP_ID_17893658 RMVar_hsa_circ_124097,RMVar_hsa_circ_108244,RMVar_hsa_circ_184740,RMVar_hsa_circ_184741,RMVar_hsa_circ_265863,RMVar_hsa_circ_113326,RMVar_hsa_circ_31587,RMVar_hsa_circ_184744,RMVar_hsa_circ_184746,RMVar_hsa_circ_82598,RMVar_hsa_circ_101650,RMVar_hsa_circ_302184,RMVar_hsa_circ_124560,RMVar_hsa_circ_184749,RMVar_hsa_circ_184750,RMVar_hsa_circ_341064,RMVar_hsa_circ_114190,RMVar_hsa_circ_184753,RMVar_hsa_circ_184754,RMVar_hsa_circ_184752 50802 RMVar_ID_50802 Human_SNP_ID_625269987 A-to-I Human chr17 - 44873516 44873516 44873516 GCTTTTGTATCTCATCTCTACAAAAATTAGCCAGGCTTGGTGGTTCATGCCTGCAGTCCCAGCTA GCTTTTGTATCTCATCTCTACAAAAATTAGCCCGGCTTGGTGGTTCATGCCTGCAGTCCCAGCTA T G EFTUD2 Ensembl:ENSG00000108883 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs920571977 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17565955 RMVar_hsa_circ_124097,RMVar_hsa_circ_108244,RMVar_hsa_circ_184740,RMVar_hsa_circ_184741,RMVar_hsa_circ_265863,RMVar_hsa_circ_113326,RMVar_hsa_circ_31587,RMVar_hsa_circ_184744,RMVar_hsa_circ_184746,RMVar_hsa_circ_82598,RMVar_hsa_circ_101650,RMVar_hsa_circ_302184,RMVar_hsa_circ_124560,RMVar_hsa_circ_184749,RMVar_hsa_circ_184750,RMVar_hsa_circ_341064,RMVar_hsa_circ_114190,RMVar_hsa_circ_184753,RMVar_hsa_circ_184754,RMVar_hsa_circ_184752 50803 RMVar_ID_50803 Human_SNP_ID_625269998 A-to-I Human chr17 - 44873578 44873577 44873579 TGGGAGGCCAAGCAGGATATTGCTTGAGCCCAAGAGTTCAAGGTTCAAGCCTGGGCAACATGGCT TGGGAGGCCAAGCAGGATATTGCTTGAGCCC__GAGTTCAAGGTTCAAGCCTGGGCAACATGGCT CTT C EFTUD2 Ensembl:ENSG00000108883 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1359632538 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_17893659 RMVar_hsa_circ_124097,RMVar_hsa_circ_108244,RMVar_hsa_circ_184740,RMVar_hsa_circ_184741,RMVar_hsa_circ_265863,RMVar_hsa_circ_113326,RMVar_hsa_circ_31587,RMVar_hsa_circ_184744,RMVar_hsa_circ_184746,RMVar_hsa_circ_82598,RMVar_hsa_circ_101650,RMVar_hsa_circ_302184,RMVar_hsa_circ_124560,RMVar_hsa_circ_184749,RMVar_hsa_circ_184750,RMVar_hsa_circ_341064,RMVar_hsa_circ_114190,RMVar_hsa_circ_184753,RMVar_hsa_circ_184754,RMVar_hsa_circ_184752 50804 RMVar_ID_50804 Human_SNP_ID_625270528 A-to-I Human chr17 - 44875707 44875707 44875707 GTACTTGGGCTGTATTAATTTCTTCTCTTTTTAGAGATAGGATCTCTGTTACCCAAGCTAGAGTG GTACTTGGGCTGTATTAATTTCTTCTCTTTTTGGAGATAGGATCTCTGTTACCCAAGCTAGAGTG T C EFTUD2 Ensembl:ENSG00000108883 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1282338504 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124097,RMVar_hsa_circ_108244,RMVar_hsa_circ_184740,RMVar_hsa_circ_184741,RMVar_hsa_circ_265863,RMVar_hsa_circ_113326,RMVar_hsa_circ_31587,RMVar_hsa_circ_184744,RMVar_hsa_circ_184746,RMVar_hsa_circ_82598,RMVar_hsa_circ_101650,RMVar_hsa_circ_302184,RMVar_hsa_circ_124560,RMVar_hsa_circ_184749,RMVar_hsa_circ_184750,RMVar_hsa_circ_341064,RMVar_hsa_circ_114190,RMVar_hsa_circ_184753,RMVar_hsa_circ_184754,RMVar_hsa_circ_184752 50805 RMVar_ID_50805 Human_SNP_ID_625273631 A-to-I Human chr17 - 44887741 44887741 44887741 AGAGTCATGCAACTGTCATCACAATCAATTTTAGAACATTTCCATTATCTCAGAAAAAAACTCCA AGAGTCATGCAACTGTCATCACAATCAATTTTGGAACATTTCCATTATCTCAGAAAAAAACTCCA T C EFTUD2 Ensembl:ENSG00000108883 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903584369 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108244,RMVar_hsa_circ_184741,RMVar_hsa_circ_265863,RMVar_hsa_circ_113326,RMVar_hsa_circ_184744 50806 RMVar_ID_50806 Human_SNP_ID_625274929 A-to-I Human chr17 - 44893234 44893234 44893234 CCTGTAGTCCCAGCTGCTTGGAAGGCCGAGGCAGGAAAATCACTTGAACACGGGAGGCGGAGGTT CCTGTAGTCCCAGCTGCTTGGAAGGCCGAGGCGGGAAAATCACTTGAACACGGGAGGCGGAGGTT T C EFTUD2 Ensembl:ENSG00000108883 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1217143914 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108244,RMVar_hsa_circ_184741,RMVar_hsa_circ_265863,RMVar_hsa_circ_113326,RMVar_hsa_circ_184744 50807 RMVar_ID_50807 Human_SNP_ID_625275187 A-to-I Human chr17 - 44894125 44894125 44894125 GCAGTCCACCTGCCTTGGCCTCCCAAACTGCTAGGATTACAGGCATGAGCCACCATGCCCAGCCC GCAGTCCACCTGCCTTGGCCTCCCAAACTGCTGGGATTACAGGCATGAGCCACCATGCCCAGCCC T C EFTUD2 Ensembl:ENSG00000108883 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs985720410 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_108244,RMVar_hsa_circ_184741,RMVar_hsa_circ_265863,RMVar_hsa_circ_113326,RMVar_hsa_circ_184744 50808 RMVar_ID_50808 Human_SNP_ID_625289129 A-to-I Human chr17 - 44944464 44944464 44944464 GCCAAGGCAGTAGATCACCTGAGGTCATGAGTATGAGACCAGCCTGACCGACATGGTGAAACCCC GCCAAGGCAGTAGATCACCTGAGGTCATGAGTGTGAGACCAGCCTGACCGACATGGTGAAACCCC T C KIF18B Ensembl:ENSG00000186185 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1205669107 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8454164,Human_RBP_ID_9862525,Human_RBP_ID_13029148,Human_RBP_ID_22952198,Human_RBP_ID_25342749 RMVar_hsa_circ_90762,RMVar_hsa_circ_184775 50809 RMVar_ID_50809 Human_SNP_ID_625289499 A-to-I Human chr17 - 44945998 44945998 44945998 CCAGGCTGGTCTTGAACTCCTGACCTCAAGCTATTCTCCTACCTCAGCTTCCCAAAGCCCTAGAA CCAGGCTGGTCTTGAACTCCTGACCTCAAGCTGTTCTCCTACCTCAGCTTCCCAAAGCCCTAGAA T C KIF18B Ensembl:ENSG00000186185 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749517636 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9862547 RMVar_hsa_circ_90762,RMVar_hsa_circ_184775 50810 RMVar_ID_50810 Human_SNP_ID_541382736 A-to-I Human chr13 - 94585104 94585104 94585104 CAGAGGTGGCAGTGAACTGAGATTGCGCCACTACACTCCAGCCTGGGCAACAGAGAGAGAGAGAA CAGAGGTGGCAGTGAACTGAGATTGCGCCACTGCACTCCAGCCTGGGCAACAGAGAGAGAGAGAA T C TGDS Ensembl:ENSG00000088451 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1001429725 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59318,RMVar_hsa_circ_164057,RMVar_hsa_circ_55020,RMVar_hsa_circ_67891,RMVar_hsa_circ_79537 50811 RMVar_ID_50811 Human_SNP_ID_541382871 A-to-I Human chr13 - 94585678 94585678 94585678 CTCGTGCTTCAGCCTACCAAGTAGCTGGGATTACAGGCGTGTGCCACCACGCCCGGTTTATTTTT CTCGTGCTTCAGCCTACCAAGTAGCTGGGATTGCAGGCGTGTGCCACCACGCCCGGTTTATTTTT T C TGDS Ensembl:ENSG00000088451 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1373154832 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59318,RMVar_hsa_circ_164057,RMVar_hsa_circ_55020,RMVar_hsa_circ_67891,RMVar_hsa_circ_79537 50812 RMVar_ID_50812 Human_SNP_ID_541383284 A-to-I Human chr13 - 94587054 94587054 94587054 ATCTTTTAAGAGTTTGATTTCTTGCTGGGTGCAGTGGCTAACACCTGTAATCCTAGCACTTTGAG ATCTTTTAAGAGTTTGATTTCTTGCTGGGTGCTGTGGCTAACACCTGTAATCCTAGCACTTTGAG T A TGDS Ensembl:ENSG00000088451 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs534724782 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6309625 RMVar_hsa_circ_59318,RMVar_hsa_circ_164057,RMVar_hsa_circ_55020,RMVar_hsa_circ_67891,RMVar_hsa_circ_79537 50813 RMVar_ID_50813 Human_SNP_ID_541383285 A-to-I Human chr13 - 94587054 94587054 94587054 ATCTTTTAAGAGTTTGATTTCTTGCTGGGTGCAGTGGCTAACACCTGTAATCCTAGCACTTTGAG ATCTTTTAAGAGTTTGATTTCTTGCTGGGTGCCGTGGCTAACACCTGTAATCCTAGCACTTTGAG T G TGDS Ensembl:ENSG00000088451 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs534724782 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6309625 RMVar_hsa_circ_59318,RMVar_hsa_circ_164057,RMVar_hsa_circ_55020,RMVar_hsa_circ_67891,RMVar_hsa_circ_79537 50814 RMVar_ID_50814 Human_SNP_ID_541384703 A-to-I Human chr13 - 94592522 94592522 94592522 CGTGAACCTGGGAGGCGGAGCTTGTGCTGAGCAGAGATTGCGCCACTGCACTACAGCCTGGGCAA CGTGAACCTGGGAGGCGGAGCTTGTGCTGAGCGGAGATTGCGCCACTGCACTACAGCCTGGGCAA T C TGDS Ensembl:ENSG00000088451 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1305995014 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67891,RMVar_hsa_circ_164059,RMVar_hsa_circ_74683,RMVar_hsa_circ_59083 50815 RMVar_ID_50815 Human_SNP_ID_541384711 A-to-I Human chr13 - 94592564 94592564 94592564 CCTGTAGTCCCAGGTACTTGGGAGGCTGAGGCAGGAGAATGGCGTGAACCTGGGAGGCGGAGCTT CCTGTAGTCCCAGGTACTTGGGAGGCTGAGGCGGGAGAATGGCGTGAACCTGGGAGGCGGAGCTT T C TGDS Ensembl:ENSG00000088451 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs955554663 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67891,RMVar_hsa_circ_164059,RMVar_hsa_circ_74683,RMVar_hsa_circ_59083 50816 RMVar_ID_50816 Human_SNP_ID_541392810 A-to-I Human chr13 + 94624594 94624594 94624594 TCGTTGTTGTTTTTGAGACGGTGTCTCGCTCTATCGCCCAGGCTGGAGTGCAGTGGCGTGATCTC TCGTTGTTGTTTTTGAGACGGTGTCTCGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCGTGATCTC A G GPR180 Ensembl:ENSG00000152749 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs558532382 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_164063,RMVar_hsa_circ_164065 50817 RMVar_ID_50817 Human_SNP_ID_541487302 A-to-I Human chr13 - 95016471 95016471 95016471 TGAGGCAGGAGAATTGCTTGAACCTGAGAGACAGAGGCTGCAGTGAGCCGAGGTCATGCCACTGC TGAGGCAGGAGAATTGCTTGAACCTGAGAGACGGAGGCTGCAGTGAGCCGAGGTCATGCCACTGC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs577432197 Functional Loss SNV dbSNP153 33..33 33 - - - 50818 RMVar_ID_50818 Human_SNP_ID_541503443 A-to-I Human chr13 - 95079753 95079753 95079753 TTGGGTCACTGCAACTTCCACCTCCCGAGTTCAAGAAATTCTCCTGTCTCAGCTTCCTGAATAGC TTGGGTCACTGCAACTTCCACCTCCCGAGTTCGAGAAATTCTCCTGTCTCAGCTTCCTGAATAGC T C ABCC4 Ensembl:ENSG00000125257 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1439797410 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4275,RMVar_hsa_circ_24477,RMVar_hsa_circ_111278,RMVar_hsa_circ_164070,RMVar_hsa_circ_287831,RMVar_hsa_circ_301609,RMVar_hsa_circ_85056,RMVar_hsa_circ_164075,RMVar_hsa_circ_164076,RMVar_hsa_circ_336783,RMVar_hsa_circ_55212,RMVar_hsa_circ_37691,RMVar_hsa_circ_49829,RMVar_hsa_circ_96604,RMVar_hsa_circ_164080,RMVar_hsa_circ_104423,RMVar_hsa_circ_304510,RMVar_hsa_circ_164081,RMVar_hsa_circ_112648,RMVar_hsa_circ_164082,RMVar_hsa_circ_164083,RMVar_hsa_circ_35420,RMVar_hsa_circ_298307,RMVar_hsa_circ_305570,RMVar_hsa_circ_377454,RMVar_hsa_circ_94694,RMVar_hsa_circ_164084,RMVar_hsa_circ_341527,RMVar_hsa_circ_13685,RMVar_hsa_circ_164086,RMVar_hsa_circ_342367 50819 RMVar_ID_50819 Human_SNP_ID_541510217 A-to-I Human chr13 - 95108771 95108771 95108771 AGAGAGATGCCAAGCATGAGCAGGGTACCTGTAGTCCCAGCTACCTGGGAGGCTGAGGCAGGAGA AGAGAGATGCCAAGCATGAGCAGGGTACCTGTGGTCCCAGCTACCTGGGAGGCTGAGGCAGGAGA T C ABCC4 Ensembl:ENSG00000125257 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1322861268 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16659,RMVar_hsa_circ_4275,RMVar_hsa_circ_24477,RMVar_hsa_circ_111278,RMVar_hsa_circ_164070,RMVar_hsa_circ_287831,RMVar_hsa_circ_85056,RMVar_hsa_circ_164076,RMVar_hsa_circ_55212,RMVar_hsa_circ_37691,RMVar_hsa_circ_49829,RMVar_hsa_circ_164080,RMVar_hsa_circ_104423,RMVar_hsa_circ_112648,RMVar_hsa_circ_164082,RMVar_hsa_circ_164083,RMVar_hsa_circ_35420,RMVar_hsa_circ_377454,RMVar_hsa_circ_94694,RMVar_hsa_circ_13685,RMVar_hsa_circ_164086,RMVar_hsa_circ_342367,RMVar_hsa_circ_294087,RMVar_hsa_circ_356649,RMVar_hsa_circ_21642,RMVar_hsa_circ_164089,RMVar_hsa_circ_115557,RMVar_hsa_circ_164087,RMVar_hsa_circ_97016,RMVar_hsa_circ_164088 50820 RMVar_ID_50820 Human_SNP_ID_541510218 A-to-I Human chr13 - 95108771 95108771 95108771 AGAGAGATGCCAAGCATGAGCAGGGTACCTGTAGTCCCAGCTACCTGGGAGGCTGAGGCAGGAGA AGAGAGATGCCAAGCATGAGCAGGGTACCTGTCGTCCCAGCTACCTGGGAGGCTGAGGCAGGAGA T G ABCC4 Ensembl:ENSG00000125257 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1322861268 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16659,RMVar_hsa_circ_4275,RMVar_hsa_circ_24477,RMVar_hsa_circ_111278,RMVar_hsa_circ_164070,RMVar_hsa_circ_287831,RMVar_hsa_circ_85056,RMVar_hsa_circ_164076,RMVar_hsa_circ_55212,RMVar_hsa_circ_37691,RMVar_hsa_circ_49829,RMVar_hsa_circ_164080,RMVar_hsa_circ_104423,RMVar_hsa_circ_112648,RMVar_hsa_circ_164082,RMVar_hsa_circ_164083,RMVar_hsa_circ_35420,RMVar_hsa_circ_377454,RMVar_hsa_circ_94694,RMVar_hsa_circ_13685,RMVar_hsa_circ_164086,RMVar_hsa_circ_342367,RMVar_hsa_circ_294087,RMVar_hsa_circ_356649,RMVar_hsa_circ_21642,RMVar_hsa_circ_164089,RMVar_hsa_circ_115557,RMVar_hsa_circ_164087,RMVar_hsa_circ_97016,RMVar_hsa_circ_164088 50821 RMVar_ID_50821 Human_SNP_ID_541516602 A-to-I Human chr13 - 95134572 95134572 95134572 GGGATTACAGGTGTGTGCCACCTCCTCCGGCTAGCTTTTGTATTTTTGTAGAGATAGAGTTTTGC GGGATTACAGGTGTGTGCCACCTCCTCCGGCTGGCTTTTGTATTTTTGTAGAGATAGAGTTTTGC T C ABCC4 Ensembl:ENSG00000125257 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1441740358 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16659,RMVar_hsa_circ_4275,RMVar_hsa_circ_24477,RMVar_hsa_circ_111278,RMVar_hsa_circ_164070,RMVar_hsa_circ_287831,RMVar_hsa_circ_85056,RMVar_hsa_circ_164076,RMVar_hsa_circ_55212,RMVar_hsa_circ_49829,RMVar_hsa_circ_164080,RMVar_hsa_circ_104423,RMVar_hsa_circ_112648,RMVar_hsa_circ_164082,RMVar_hsa_circ_164083,RMVar_hsa_circ_35420,RMVar_hsa_circ_94694,RMVar_hsa_circ_13685,RMVar_hsa_circ_164086,RMVar_hsa_circ_342367,RMVar_hsa_circ_294087,RMVar_hsa_circ_356649,RMVar_hsa_circ_21642,RMVar_hsa_circ_164092,RMVar_hsa_circ_79132,RMVar_hsa_circ_164089,RMVar_hsa_circ_115557,RMVar_hsa_circ_164087,RMVar_hsa_circ_97016,RMVar_hsa_circ_340829,RMVar_hsa_circ_343242,RMVar_hsa_circ_374098,RMVar_hsa_circ_164088,RMVar_hsa_circ_362701,RMVar_hsa_circ_341344,RMVar_hsa_circ_274118,RMVar_hsa_circ_312838,RMVar_hsa_circ_272357,RMVar_hsa_circ_164094,RMVar_hsa_circ_48908,RMVar_hsa_circ_164095,RMVar_hsa_circ_164093,RMVar_hsa_circ_164090,RMVar_hsa_circ_164091 50822 RMVar_ID_50822 Human_SNP_ID_541537621 A-to-I Human chr13 - 95218655 95218655 95218655 TGTAGACAGGATCTCACTACGTTGCCCAGTCTAGTCTTGAACTCCTGGGCTCATGTGATCTTGCC TGTAGACAGGATCTCACTACGTTGCCCAGTCTGGTCTTGAACTCCTGGGCTCATGTGATCTTGCC T C ABCC4 Ensembl:ENSG00000125257 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs952296708 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25069791 RMVar_hsa_circ_95851,RMVar_hsa_circ_164104,RMVar_hsa_circ_28224,RMVar_hsa_circ_8988,RMVar_hsa_circ_267547,RMVar_hsa_circ_81497,RMVar_hsa_circ_164118,RMVar_hsa_circ_356247,RMVar_hsa_circ_282890,RMVar_hsa_circ_164123,RMVar_hsa_circ_164124,RMVar_hsa_circ_164125,RMVar_hsa_circ_164126,RMVar_hsa_circ_326259 50823 RMVar_ID_50823 Human_SNP_ID_541550365 A-to-I Human chr13 - 95269344 95269344 95269344 TCAGCTCACTGCAGCCTCCACCTCCTGTGTTCAAGCAGTCCTCCTGCCTCAGCCACCAGACTAGC TCAGCTCACTGCAGCCTCCACCTCCTGTGTTCGAGCAGTCCTCCTGCCTCAGCCACCAGACTAGC T C ABCC4 Ensembl:ENSG00000125257 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1253239487 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1475500,Human_Splice_Rec_1475501,Human_Splice_Rec_1475532,Human_Splice_Rec_1475533 RMVar_hsa_circ_95851,RMVar_hsa_circ_164104,RMVar_hsa_circ_81497,RMVar_hsa_circ_164125 50824 RMVar_ID_50824 Human_SNP_ID_541553929 A-to-I Human chr13 - 95283052 95283052 95283052 GCCACCGCGCCAGGCTAATTTTTTGTATTTTTAGTAGAGATGGGGTTTCACTGTGTTGACCAGGA GCCACCGCGCCAGGCTAATTTTTTGTATTTTTGGTAGAGATGGGGTTTCACTGTGTTGACCAGGA T C ABCC4 Ensembl:ENSG00000125257 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1033851869 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95851,RMVar_hsa_circ_164104,RMVar_hsa_circ_81497,RMVar_hsa_circ_164125 50825 RMVar_ID_50825 Human_SNP_ID_541553930 A-to-I Human chr13 - 95283052 95283052 95283052 GCCACCGCGCCAGGCTAATTTTTTGTATTTTTAGTAGAGATGGGGTTTCACTGTGTTGACCAGGA GCCACCGCGCCAGGCTAATTTTTTGTATTTTTCGTAGAGATGGGGTTTCACTGTGTTGACCAGGA T G ABCC4 Ensembl:ENSG00000125257 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1033851869 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95851,RMVar_hsa_circ_164104,RMVar_hsa_circ_81497,RMVar_hsa_circ_164125 50826 RMVar_ID_50826 Human_SNP_ID_541554747 A-to-I Human chr13 - 95286323 95286323 95286323 CTGAGGTCAGGAGTTGGAGATCAGCCTGGCCAACATAGTGGAACCCTGACTTTACTAAAAATACA CTGAGGTCAGGAGTTGGAGATCAGCCTGGCCACCATAGTGGAACCCTGACTTTACTAAAAATACA T G ABCC4 Ensembl:ENSG00000125257 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232579796 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95851,RMVar_hsa_circ_164104,RMVar_hsa_circ_81497,RMVar_hsa_circ_164125 50827 RMVar_ID_50827 Human_SNP_ID_541556596 A-to-I Human chr13 - 95293210 95293210 95293210 GGGATTACAGATGTGCACCACCAGGCCTGGCTAATTTTTTTGTTGTTGTTAGAGACAGGGTTTTG GGGATTACAGATGTGCACCACCAGGCCTGGCTGATTTTTTTGTTGTTGTTAGAGACAGGGTTTTG T C ABCC4 Ensembl:ENSG00000125257 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1043505012 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12242657 RMVar_hsa_circ_95851,RMVar_hsa_circ_164104,RMVar_hsa_circ_81497,RMVar_hsa_circ_164125 50828 RMVar_ID_50828 Human_SNP_ID_541556990 A-to-I Human chr13 - 95294806 95294806 95294806 GGGACTACAGATGTGCGCCACCATGCTCAGCTAATTTTTTGTACTTTTAGGAGAGATGGGGTTTC GGGACTACAGATGTGCGCCACCATGCTCAGCTGATTTTTTGTACTTTTAGGAGAGATGGGGTTTC T C ABCC4 Ensembl:ENSG00000125257 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs541735957 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95851,RMVar_hsa_circ_164104,RMVar_hsa_circ_81497,RMVar_hsa_circ_164125 50829 RMVar_ID_50829 Human_SNP_ID_541629882 A-to-I Human chr13 - 95584085 95584085 95584085 GTAGTCCTAGCTACTTGGGAGGCTAAGGCAGGAGAATTGCTTGAACCTGGGAAGTGGAGGTTGCA GTAGTCCTAGCTACTTGGGAGGCTAAGGCAGGGGAATTGCTTGAACCTGGGAAGTGGAGGTTGCA T C DZIP1 Ensembl:ENSG00000134874 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1015544357 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_164131,RMVar_hsa_circ_164130 50830 RMVar_ID_50830 Human_SNP_ID_541661485 A-to-I Human chr13 + 95711314 95711314 95711314 GAGGTCAGGAGTTTGGGACCAGCCCGGACAACATGGTGAAACTTGTCTCTACTAAAAATATAAAA GAGGTCAGGAGTTTGGGACCAGCCCGGACAACGTGGTGAAACTTGTCTCTACTAAAAATATAAAA A G DNAJC3 Ensembl:ENSG00000102580 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1037395249 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10203,RMVar_hsa_circ_58755,RMVar_hsa_circ_348070,RMVar_hsa_circ_327356,RMVar_hsa_circ_21849 50831 RMVar_ID_50831 Human_SNP_ID_541672501 A-to-I Human chr13 + 95755255 95755255 95755255 ATCACCTGAGGCCCGGAGTTGGAGACCAGCCTAGGCAACATAGTGAGACAACCCTGTCTCTACAA ATCACCTGAGGCCCGGAGTTGGAGACCAGCCTCGGCAACATAGTGAGACAACCCTGTCTCTACAA A C DNAJC3 Ensembl:ENSG00000102580 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs751350945 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58755,RMVar_hsa_circ_348070,RMVar_hsa_circ_21849,RMVar_hsa_circ_113390,RMVar_hsa_circ_364900,RMVar_hsa_circ_90174,RMVar_hsa_circ_164153,RMVar_hsa_circ_164155 50832 RMVar_ID_50832 Human_SNP_ID_541681811 A-to-I Human chr13 + 95793383 95793363 95793384 GTGACTGAGAAGCAGCCTGGGTGTGTAAAGAGATAGTCATTCCCCCTGCCTGTCTCACTGTAGGG GTGACTGAGAAGC_____________________AGTCATTCCCCCTGCCTGTCTCACTGTAGGG CAGCCTGGGTGTGTAAAGAGAT C DNAJC3 Ensembl:ENSG00000102580 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs11274423 Functional Loss DEL dbSNP153 14..34 33 - - - Human_RBP_ID_17477707 50833 RMVar_ID_50833 Human_SNP_ID_541681811 A-to-I Human chr13 - 95793384 95793363 95793384 ACCCTACAGTGAGACAGGCAGGGGGAATGACTATCTCTTTACACACCCAGGCTGCTTCTCAGTCA ACCCTACAGTGAGACAGGCAGGGGGAATGACT_____________________GCTTCTCAGTCA CAGCCTGGGTGTGTAAAGAGAT C - - Other Unknown GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs11274423 Functional Loss DEL dbSNP153 33..53 33 - - - 50834 RMVar_ID_50834 Human_SNP_ID_541713872 A-to-I Human chr13 - 95922655 95922655 95922655 ATCACACCCAGCAAATTTTTGTATTTTTTTGTAGAGACGGGTTTTGCCATGTCATCCAGGCTGGT ATCACACCCAGCAAATTTTTGTATTTTTTTGTGGAGACGGGTTTTGCCATGTCATCCAGGCTGGT T C UGGT2 Ensembl:ENSG00000102595 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1437264841 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2789,RMVar_hsa_circ_335904,RMVar_hsa_circ_127695,RMVar_hsa_circ_19524,RMVar_hsa_circ_164163,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_324538,RMVar_hsa_circ_305027,RMVar_hsa_circ_286111,RMVar_hsa_circ_23637,RMVar_hsa_circ_7015,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_164193,RMVar_hsa_circ_42703,RMVar_hsa_circ_124797,RMVar_hsa_circ_111503,RMVar_hsa_circ_164195,RMVar_hsa_circ_164196,RMVar_hsa_circ_23854,RMVar_hsa_circ_164197,RMVar_hsa_circ_303776 50835 RMVar_ID_50835 Human_SNP_ID_541728398 A-to-I Human chr13 - 95978292 95978292 95978292 CATACAGATGGCCAACAGTGATGCTCACCATCACTAATCGTCAGGGAAATGCAAATCAAAACCAC CATACAGATGGCCAACAGTGATGCTCACCATCGCTAATCGTCAGGGAAATGCAAATCAAAACCAC T C UGGT2 Ensembl:ENSG00000102595 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1159095225 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_335904,RMVar_hsa_circ_94440,RMVar_hsa_circ_164173,RMVar_hsa_circ_100158,RMVar_hsa_circ_46949,RMVar_hsa_circ_7338,RMVar_hsa_circ_164176,RMVar_hsa_circ_351932,RMVar_hsa_circ_305027,RMVar_hsa_circ_286111,RMVar_hsa_circ_23637,RMVar_hsa_circ_124128,RMVar_hsa_circ_7015,RMVar_hsa_circ_7299,RMVar_hsa_circ_111503,RMVar_hsa_circ_164196,RMVar_hsa_circ_294431,RMVar_hsa_circ_331324,RMVar_hsa_circ_370887,RMVar_hsa_circ_321524,RMVar_hsa_circ_275432,RMVar_hsa_circ_164201,RMVar_hsa_circ_18577,RMVar_hsa_circ_346801,RMVar_hsa_circ_164199,RMVar_hsa_circ_164200,RMVar_hsa_circ_164198,RMVar_hsa_circ_370326,RMVar_hsa_circ_333773,RMVar_hsa_circ_31325,RMVar_hsa_circ_44063,RMVar_hsa_circ_34143,RMVar_hsa_circ_164209,RMVar_hsa_circ_164210,RMVar_hsa_circ_164208,RMVar_hsa_circ_277199,RMVar_hsa_circ_11715,RMVar_hsa_circ_321520,RMVar_hsa_circ_351525,RMVar_hsa_circ_53384,RMVar_hsa_circ_338179,RMVar_hsa_circ_355550,RMVar_hsa_circ_370070,RMVar_hsa_circ_335109,RMVar_hsa_circ_279346,RMVar_hsa_circ_164213,RMVar_hsa_circ_164215,RMVar_hsa_circ_270842,RMVar_hsa_circ_164214,RMVar_hsa_circ_164211,RMVar_hsa_circ_164212,RMVar_hsa_circ_26358 50836 RMVar_ID_50836 Human_SNP_ID_541728880 A-to-I Human chr13 - 95980183 95980182 95980183 GCATATTGTTCTGCTATAAACATGCATATGCAAGTATCTTTTTCATATAATGACTTCCCCCCCAC GCATATTGTTCTGCTATAAACATGCATATGCA_GTATCTTTTTCATATAATGACTTCCCCCCCAC CT C UGGT2 Ensembl:ENSG00000102595 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1163174599 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_335904,RMVar_hsa_circ_94440,RMVar_hsa_circ_164173,RMVar_hsa_circ_100158,RMVar_hsa_circ_46949,RMVar_hsa_circ_7338,RMVar_hsa_circ_164176,RMVar_hsa_circ_351932,RMVar_hsa_circ_305027,RMVar_hsa_circ_286111,RMVar_hsa_circ_23637,RMVar_hsa_circ_124128,RMVar_hsa_circ_7015,RMVar_hsa_circ_7299,RMVar_hsa_circ_111503,RMVar_hsa_circ_164196,RMVar_hsa_circ_294431,RMVar_hsa_circ_331324,RMVar_hsa_circ_370887,RMVar_hsa_circ_321524,RMVar_hsa_circ_275432,RMVar_hsa_circ_164201,RMVar_hsa_circ_18577,RMVar_hsa_circ_346801,RMVar_hsa_circ_164199,RMVar_hsa_circ_164200,RMVar_hsa_circ_164198,RMVar_hsa_circ_370326,RMVar_hsa_circ_333773,RMVar_hsa_circ_31325,RMVar_hsa_circ_44063,RMVar_hsa_circ_34143,RMVar_hsa_circ_164209,RMVar_hsa_circ_164210,RMVar_hsa_circ_164208,RMVar_hsa_circ_277199,RMVar_hsa_circ_11715,RMVar_hsa_circ_321520,RMVar_hsa_circ_351525,RMVar_hsa_circ_53384,RMVar_hsa_circ_338179,RMVar_hsa_circ_355550,RMVar_hsa_circ_370070,RMVar_hsa_circ_335109,RMVar_hsa_circ_279346,RMVar_hsa_circ_164213,RMVar_hsa_circ_164215,RMVar_hsa_circ_270842,RMVar_hsa_circ_164214,RMVar_hsa_circ_164211,RMVar_hsa_circ_164212,RMVar_hsa_circ_26358 50837 RMVar_ID_50837 Human_SNP_ID_541729955 A-to-I Human chr13 - 95984407 95984407 95984407 GGAGAATCACTTGAGCCCAGGAACCCGAGACTACAGTGAGTTGTGATCATGCCACTGCAGTCCTG GGAGAATCACTTGAGCCCAGGAACCCGAGACTGCAGTGAGTTGTGATCATGCCACTGCAGTCCTG T C UGGT2 Ensembl:ENSG00000102595 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1405624598 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_335904,RMVar_hsa_circ_94440,RMVar_hsa_circ_164173,RMVar_hsa_circ_100158,RMVar_hsa_circ_46949,RMVar_hsa_circ_7338,RMVar_hsa_circ_164176,RMVar_hsa_circ_351932,RMVar_hsa_circ_305027,RMVar_hsa_circ_286111,RMVar_hsa_circ_23637,RMVar_hsa_circ_124128,RMVar_hsa_circ_7299,RMVar_hsa_circ_111503,RMVar_hsa_circ_164196,RMVar_hsa_circ_294431,RMVar_hsa_circ_331324,RMVar_hsa_circ_370887,RMVar_hsa_circ_321524,RMVar_hsa_circ_275432,RMVar_hsa_circ_164201,RMVar_hsa_circ_18577,RMVar_hsa_circ_164199,RMVar_hsa_circ_164200,RMVar_hsa_circ_164198,RMVar_hsa_circ_370326,RMVar_hsa_circ_333773,RMVar_hsa_circ_31325,RMVar_hsa_circ_44063,RMVar_hsa_circ_34143,RMVar_hsa_circ_164209,RMVar_hsa_circ_164210,RMVar_hsa_circ_164208,RMVar_hsa_circ_17170,RMVar_hsa_circ_277199,RMVar_hsa_circ_11715,RMVar_hsa_circ_321520,RMVar_hsa_circ_338179,RMVar_hsa_circ_355550,RMVar_hsa_circ_370070,RMVar_hsa_circ_335109,RMVar_hsa_circ_279346,RMVar_hsa_circ_164213,RMVar_hsa_circ_164215,RMVar_hsa_circ_270842,RMVar_hsa_circ_164214,RMVar_hsa_circ_352119,RMVar_hsa_circ_164211,RMVar_hsa_circ_164212,RMVar_hsa_circ_368539,RMVar_hsa_circ_26358,RMVar_hsa_circ_365881,RMVar_hsa_circ_297645,RMVar_hsa_circ_326902,RMVar_hsa_circ_282588,RMVar_hsa_circ_164216,RMVar_hsa_circ_164217,RMVar_hsa_circ_164218 50838 RMVar_ID_50838 Human_SNP_ID_541731599 A-to-I Human chr13 - 95990979 95990979 95990979 TCATTCTCAGCAAACTAACACAGGAACAGAAAACCAAACACCACATGTTCTTACTCAAAAGTGGG TCATTCTCAGCAAACTAACACAGGAACAGAAACCCAAACACCACATGTTCTTACTCAAAAGTGGG T G UGGT2 Ensembl:ENSG00000102595 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs933351355 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94440,RMVar_hsa_circ_164173,RMVar_hsa_circ_100158,RMVar_hsa_circ_46949,RMVar_hsa_circ_7338,RMVar_hsa_circ_164176,RMVar_hsa_circ_305027,RMVar_hsa_circ_286111,RMVar_hsa_circ_124128,RMVar_hsa_circ_111503,RMVar_hsa_circ_164196,RMVar_hsa_circ_370887,RMVar_hsa_circ_321524,RMVar_hsa_circ_275432,RMVar_hsa_circ_18577,RMVar_hsa_circ_164199,RMVar_hsa_circ_164200,RMVar_hsa_circ_164198,RMVar_hsa_circ_370326,RMVar_hsa_circ_333773,RMVar_hsa_circ_44063,RMVar_hsa_circ_164209,RMVar_hsa_circ_164210,RMVar_hsa_circ_17170,RMVar_hsa_circ_277199,RMVar_hsa_circ_321520,RMVar_hsa_circ_338179,RMVar_hsa_circ_370070,RMVar_hsa_circ_279346,RMVar_hsa_circ_164213,RMVar_hsa_circ_164215,RMVar_hsa_circ_270842,RMVar_hsa_circ_164214,RMVar_hsa_circ_352119,RMVar_hsa_circ_164212,RMVar_hsa_circ_365881,RMVar_hsa_circ_297645,RMVar_hsa_circ_282588,RMVar_hsa_circ_96243,RMVar_hsa_circ_106896,RMVar_hsa_circ_164216,RMVar_hsa_circ_164217,RMVar_hsa_circ_164218,RMVar_hsa_circ_164222,RMVar_hsa_circ_289770,RMVar_hsa_circ_319372,RMVar_hsa_circ_164220,RMVar_hsa_circ_304186,RMVar_hsa_circ_164223,RMVar_hsa_circ_164221,RMVar_hsa_circ_164224 50839 RMVar_ID_50839 Human_SNP_ID_541731646 A-to-I Human chr13 - 95991193 95991193 95991193 AAGGATTATAAATCATTCTACTATAAAGACACATGCACACGTATGTTGATTGTAGCACTATTCAC AAGGATTATAAATCATTCTACTATAAAGACACGTGCACACGTATGTTGATTGTAGCACTATTCAC T C UGGT2 Ensembl:ENSG00000102595 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs375807812 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_94440,RMVar_hsa_circ_164173,RMVar_hsa_circ_100158,RMVar_hsa_circ_46949,RMVar_hsa_circ_7338,RMVar_hsa_circ_164176,RMVar_hsa_circ_305027,RMVar_hsa_circ_286111,RMVar_hsa_circ_124128,RMVar_hsa_circ_111503,RMVar_hsa_circ_164196,RMVar_hsa_circ_370887,RMVar_hsa_circ_321524,RMVar_hsa_circ_275432,RMVar_hsa_circ_18577,RMVar_hsa_circ_164199,RMVar_hsa_circ_164200,RMVar_hsa_circ_164198,RMVar_hsa_circ_370326,RMVar_hsa_circ_333773,RMVar_hsa_circ_44063,RMVar_hsa_circ_164209,RMVar_hsa_circ_164210,RMVar_hsa_circ_17170,RMVar_hsa_circ_277199,RMVar_hsa_circ_321520,RMVar_hsa_circ_338179,RMVar_hsa_circ_370070,RMVar_hsa_circ_279346,RMVar_hsa_circ_164213,RMVar_hsa_circ_164215,RMVar_hsa_circ_270842,RMVar_hsa_circ_164214,RMVar_hsa_circ_352119,RMVar_hsa_circ_164212,RMVar_hsa_circ_365881,RMVar_hsa_circ_297645,RMVar_hsa_circ_282588,RMVar_hsa_circ_96243,RMVar_hsa_circ_106896,RMVar_hsa_circ_164216,RMVar_hsa_circ_164217,RMVar_hsa_circ_164218,RMVar_hsa_circ_164222,RMVar_hsa_circ_289770,RMVar_hsa_circ_319372,RMVar_hsa_circ_164220,RMVar_hsa_circ_304186,RMVar_hsa_circ_164223,RMVar_hsa_circ_164221,RMVar_hsa_circ_164224 50840 RMVar_ID_50840 Human_SNP_ID_541731681 A-to-I Human chr13 - 95991328 95991327 95991329 TAGGAAGGCTTTTACACTGTTGGTGTGTGTGTAGATGAGTTCAACCGTTGTGGAAGACAGTGTGG TAGGAAGGCTTTTACACTGTTGGTGTGTGTG__GATGAGTTCAACCGTTGTGGAAGACAGTGTGG CTA C UGGT2 Ensembl:ENSG00000102595 Protein coding intron GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs957593075 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_12245622 RMVar_hsa_circ_94440,RMVar_hsa_circ_164173,RMVar_hsa_circ_100158,RMVar_hsa_circ_46949,RMVar_hsa_circ_7338,RMVar_hsa_circ_164176,RMVar_hsa_circ_305027,RMVar_hsa_circ_286111,RMVar_hsa_circ_124128,RMVar_hsa_circ_111503,RMVar_hsa_circ_164196,RMVar_hsa_circ_370887,RMVar_hsa_circ_321524,RMVar_hsa_circ_275432,RMVar_hsa_circ_18577,RMVar_hsa_circ_164199,RMVar_hsa_circ_164200,RMVar_hsa_circ_164198,RMVar_hsa_circ_370326,RMVar_hsa_circ_333773,RMVar_hsa_circ_44063,RMVar_hsa_circ_164209,RMVar_hsa_circ_164210,RMVar_hsa_circ_17170,RMVar_hsa_circ_277199,RMVar_hsa_circ_321520,RMVar_hsa_circ_338179,RMVar_hsa_circ_370070,RMVar_hsa_circ_279346,RMVar_hsa_circ_164213,RMVar_hsa_circ_164215,RMVar_hsa_circ_270842,RMVar_hsa_circ_164214,RMVar_hsa_circ_352119,RMVar_hsa_circ_164212,RMVar_hsa_circ_365881,RMVar_hsa_circ_297645,RMVar_hsa_circ_282588,RMVar_hsa_circ_96243,RMVar_hsa_circ_106896,RMVar_hsa_circ_164216,RMVar_hsa_circ_164217,RMVar_hsa_circ_164218,RMVar_hsa_circ_164222,RMVar_hsa_circ_289770,RMVar_hsa_circ_319372,RMVar_hsa_circ_164220,RMVar_hsa_circ_304186,RMVar_hsa_circ_164223,RMVar_hsa_circ_164221,RMVar_hsa_circ_164224 50841 RMVar_ID_50841 Human_SNP_ID_541731683 A-to-I Human chr13 - 95991328 95991328 95991328 TAGGAAGGCTTTTACACTGTTGGTGTGTGTGTAGATGAGTTCAACCGTTGTGGAAGACAGTGTGG TAGGAAGGCTTTTACACTGTTGGTGTGTGTGTGGATGAGTTCAACCGTTGTGGAAGACAGTGTGG T C UGGT2 Ensembl:ENSG00000102595 Protein coding intron GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs1360834069 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12245622 RMVar_hsa_circ_94440,RMVar_hsa_circ_164173,RMVar_hsa_circ_100158,RMVar_hsa_circ_46949,RMVar_hsa_circ_7338,RMVar_hsa_circ_164176,RMVar_hsa_circ_305027,RMVar_hsa_circ_286111,RMVar_hsa_circ_124128,RMVar_hsa_circ_111503,RMVar_hsa_circ_164196,RMVar_hsa_circ_370887,RMVar_hsa_circ_321524,RMVar_hsa_circ_275432,RMVar_hsa_circ_18577,RMVar_hsa_circ_164199,RMVar_hsa_circ_164200,RMVar_hsa_circ_164198,RMVar_hsa_circ_370326,RMVar_hsa_circ_333773,RMVar_hsa_circ_44063,RMVar_hsa_circ_164209,RMVar_hsa_circ_164210,RMVar_hsa_circ_17170,RMVar_hsa_circ_277199,RMVar_hsa_circ_321520,RMVar_hsa_circ_338179,RMVar_hsa_circ_370070,RMVar_hsa_circ_279346,RMVar_hsa_circ_164213,RMVar_hsa_circ_164215,RMVar_hsa_circ_270842,RMVar_hsa_circ_164214,RMVar_hsa_circ_352119,RMVar_hsa_circ_164212,RMVar_hsa_circ_365881,RMVar_hsa_circ_297645,RMVar_hsa_circ_282588,RMVar_hsa_circ_96243,RMVar_hsa_circ_106896,RMVar_hsa_circ_164216,RMVar_hsa_circ_164217,RMVar_hsa_circ_164218,RMVar_hsa_circ_164222,RMVar_hsa_circ_289770,RMVar_hsa_circ_319372,RMVar_hsa_circ_164220,RMVar_hsa_circ_304186,RMVar_hsa_circ_164223,RMVar_hsa_circ_164221,RMVar_hsa_circ_164224 50842 RMVar_ID_50842 Human_SNP_ID_541731691 A-to-I Human chr13 - 95991361 95991361 95991361 GAAACGACAGATGCTGGAGGGGATGTGGAGAAATAGGAAGGCTTTTACACTGTTGGTGTGTGTGT GAAACGACAGATGCTGGAGGGGATGTGGAGAAGTAGGAAGGCTTTTACACTGTTGGTGTGTGTGT T C UGGT2 Ensembl:ENSG00000102595 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs553120136 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12245623 RMVar_hsa_circ_94440,RMVar_hsa_circ_164173,RMVar_hsa_circ_100158,RMVar_hsa_circ_46949,RMVar_hsa_circ_7338,RMVar_hsa_circ_164176,RMVar_hsa_circ_305027,RMVar_hsa_circ_286111,RMVar_hsa_circ_124128,RMVar_hsa_circ_111503,RMVar_hsa_circ_164196,RMVar_hsa_circ_370887,RMVar_hsa_circ_321524,RMVar_hsa_circ_275432,RMVar_hsa_circ_18577,RMVar_hsa_circ_164199,RMVar_hsa_circ_164200,RMVar_hsa_circ_164198,RMVar_hsa_circ_370326,RMVar_hsa_circ_333773,RMVar_hsa_circ_44063,RMVar_hsa_circ_164209,RMVar_hsa_circ_164210,RMVar_hsa_circ_17170,RMVar_hsa_circ_277199,RMVar_hsa_circ_321520,RMVar_hsa_circ_338179,RMVar_hsa_circ_370070,RMVar_hsa_circ_279346,RMVar_hsa_circ_164213,RMVar_hsa_circ_164215,RMVar_hsa_circ_270842,RMVar_hsa_circ_164214,RMVar_hsa_circ_352119,RMVar_hsa_circ_164212,RMVar_hsa_circ_365881,RMVar_hsa_circ_297645,RMVar_hsa_circ_282588,RMVar_hsa_circ_96243,RMVar_hsa_circ_106896,RMVar_hsa_circ_164216,RMVar_hsa_circ_164217,RMVar_hsa_circ_164218,RMVar_hsa_circ_164222,RMVar_hsa_circ_289770,RMVar_hsa_circ_319372,RMVar_hsa_circ_164220,RMVar_hsa_circ_304186,RMVar_hsa_circ_164223,RMVar_hsa_circ_164221,RMVar_hsa_circ_164224 50843 RMVar_ID_50843 Human_SNP_ID_541731706 A-to-I Human chr13 - 95991421 95991421 95991421 AAATACGTGTTTTCAATGAGACACCATCTCACACCAGTTAGAATGACAATCATTAAAAAGGAAAC AAATACGTGTTTTCAATGAGACACCATCTCACGCCAGTTAGAATGACAATCATTAAAAAGGAAAC T C UGGT2 Ensembl:ENSG00000102595 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1186300594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1476058 RMVar_hsa_circ_94440,RMVar_hsa_circ_164173,RMVar_hsa_circ_100158,RMVar_hsa_circ_46949,RMVar_hsa_circ_7338,RMVar_hsa_circ_164176,RMVar_hsa_circ_305027,RMVar_hsa_circ_286111,RMVar_hsa_circ_124128,RMVar_hsa_circ_111503,RMVar_hsa_circ_164196,RMVar_hsa_circ_370887,RMVar_hsa_circ_321524,RMVar_hsa_circ_275432,RMVar_hsa_circ_18577,RMVar_hsa_circ_164199,RMVar_hsa_circ_164200,RMVar_hsa_circ_164198,RMVar_hsa_circ_370326,RMVar_hsa_circ_333773,RMVar_hsa_circ_44063,RMVar_hsa_circ_164209,RMVar_hsa_circ_164210,RMVar_hsa_circ_17170,RMVar_hsa_circ_277199,RMVar_hsa_circ_321520,RMVar_hsa_circ_338179,RMVar_hsa_circ_370070,RMVar_hsa_circ_279346,RMVar_hsa_circ_164213,RMVar_hsa_circ_164215,RMVar_hsa_circ_270842,RMVar_hsa_circ_164214,RMVar_hsa_circ_352119,RMVar_hsa_circ_164212,RMVar_hsa_circ_365881,RMVar_hsa_circ_297645,RMVar_hsa_circ_282588,RMVar_hsa_circ_96243,RMVar_hsa_circ_106896,RMVar_hsa_circ_164216,RMVar_hsa_circ_164217,RMVar_hsa_circ_164218,RMVar_hsa_circ_164222,RMVar_hsa_circ_289770,RMVar_hsa_circ_319372,RMVar_hsa_circ_164220,RMVar_hsa_circ_304186,RMVar_hsa_circ_164223,RMVar_hsa_circ_164221,RMVar_hsa_circ_164224 50844 RMVar_ID_50844 Human_SNP_ID_541740726 A-to-I Human chr13 - 96029490 96029490 96029490 CTTGAGGCCAGGAGTTCGAGACCAGCCTGGCCAACATTGTGAGACCCCGTCTCTACTGAAAATAC CTTGAGGCCAGGAGTTCGAGACCAGCCTGGCCCACATTGTGAGACCCCGTCTCTACTGAAAATAC T G UGGT2 Ensembl:ENSG00000102595 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs761077211 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100158,RMVar_hsa_circ_164176,RMVar_hsa_circ_124128,RMVar_hsa_circ_370887,RMVar_hsa_circ_164198,RMVar_hsa_circ_164210,RMVar_hsa_circ_17170,RMVar_hsa_circ_370070,RMVar_hsa_circ_164215,RMVar_hsa_circ_280623,RMVar_hsa_circ_164227 50845 RMVar_ID_50845 Human_SNP_ID_541855900 A-to-I Human chr13 + 96514546 96514546 96514546 GATGAGGTCATAAGGGTGGGCCCTGATCTGATAGTATTAGTGGCCTTAGAAGAAGAGGAGGTCAT GATGAGGTCATAAGGGTGGGCCCTGATCTGATGGTATTAGTGGCCTTAGAAGAAGAGGAGGTCAT A G HS6ST3 Ensembl:ENSG00000185352 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1370570516 Functional Loss SNV dbSNP153 33..33 33 - - - 50846 RMVar_ID_50846 Human_SNP_ID_541856331 A-to-I Human chr13 + 96516141 96516141 96516141 TGGAGTGCAGTGGGGTGATGTCGGCTCAATGCAACCTCTGCCTCCTTGGTTCAAGCGATTCTCCT TGGAGTGCAGTGGGGTGATGTCGGCTCAATGCGACCTCTGCCTCCTTGGTTCAAGCGATTCTCCT A G HS6ST3 Ensembl:ENSG00000185352 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170021586 Functional Loss SNV dbSNP153 33..33 33 - - - 50847 RMVar_ID_50847 Human_SNP_ID_541866783 A-to-I Human chr13 + 96562256 96562256 96562256 ACAATATGGATGCAGCTGGTGGCCATTATCCTAAGCAAATTAACACAGAATCAGAAAACCAAATA ACAATATGGATGCAGCTGGTGGCCATTATCCTGAGCAAATTAACACAGAATCAGAAAACCAAATA A G HS6ST3 Ensembl:ENSG00000185352 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs530117685 Functional Loss SNV dbSNP153 33..33 33 - - - 50848 RMVar_ID_50848 Human_SNP_ID_541874715 A-to-I Human chr13 + 96596388 96596388 96596388 CATCAGTTGATGAGCAGTTAGGTTGATATAATATCTTTGAAATTGTAAATTGTGCTGCAATAAAC CATCAGTTGATGAGCAGTTAGGTTGATATAATGTCTTTGAAATTGTAAATTGTGCTGCAATAAAC A G HS6ST3 Ensembl:ENSG00000185352 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs750798945 Functional Loss SNV dbSNP153 33..33 33 - - - 50849 RMVar_ID_50849 Human_SNP_ID_541888732 A-to-I Human chr13 + 96657319 96657319 96657319 ACAGTGGCTCACACCTATAATCTCAGCACTTTAGGAGACTGCAGTGGGAAGATCACTTGAGCCCA ACAGTGGCTCACACCTATAATCTCAGCACTTTGGGAGACTGCAGTGGGAAGATCACTTGAGCCCA A G HS6ST3 Ensembl:ENSG00000185352 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs773146343 Functional Loss SNV dbSNP153 33..33 33 - - - 50850 RMVar_ID_50850 Human_SNP_ID_542042546 A-to-I Human chr13 + 97291748 97291748 97291748 GAAAACCCTTCTCTGCTAAAAATACAAAAATTAGCTGGGCATGGTGGCATGCACCTGTAATCCCA GAAAACCCTTCTCTGCTAAAAATACAAAAATTGGCTGGGCATGGTGGCATGCACCTGTAATCCCA A G MBNL2 Ensembl:ENSG00000139793 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs931214018 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 50851 RMVar_ID_50851 Human_SNP_ID_542042559 A-to-I Human chr13 + 97291788 97291788 97291788 ATGGTGGCATGCACCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACCTG ATGGTGGCATGCACCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCTG A G MBNL2 Ensembl:ENSG00000139793 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs887756233 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 50852 RMVar_ID_50852 Human_SNP_ID_542055701 A-to-I Human chr13 + 97348249 97348249 97348249 CCCATCTAAGTTCTAATTTTTTTTGTAGAGACAGGGTCTCACCATGTTGTCCAGGCTAGTCTCAA CCCATCTAAGTTCTAATTTTTTTTGTAGAGACCGGGTCTCACCATGTTGTCCAGGCTAGTCTCAA A C MBNL2 Ensembl:ENSG00000139793 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs771353728 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12253926 RMVar_hsa_circ_112135,RMVar_hsa_circ_105674,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_371028,RMVar_hsa_circ_115054,RMVar_hsa_circ_164238,RMVar_hsa_circ_164239,RMVar_hsa_circ_164237,RMVar_hsa_circ_352018,RMVar_hsa_circ_164243,RMVar_hsa_circ_274860,RMVar_hsa_circ_164240,RMVar_hsa_circ_295062,RMVar_hsa_circ_164244,RMVar_hsa_circ_121605,RMVar_hsa_circ_119458,RMVar_hsa_circ_164245,RMVar_hsa_circ_164246,RMVar_hsa_circ_164247 50853 RMVar_ID_50853 Human_SNP_ID_542056003 A-to-I Human chr13 + 97349527 97349523 97349527 ACTAAGAACACATTTTTCCACAAAATTTGTTTATTTATTTGTTTTTTGAGACAGAGTCTTGCTCT ACTAAGAACACATTTTTCCACAAAATTTG____TTTATTTGTTTTTTGAGACAGAGTCTTGCTCT GTTTA G MBNL2 Ensembl:ENSG00000139793 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1009103558 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_12264266 RMVar_hsa_circ_112135,RMVar_hsa_circ_105674,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_371028,RMVar_hsa_circ_115054,RMVar_hsa_circ_164238,RMVar_hsa_circ_164239,RMVar_hsa_circ_164237,RMVar_hsa_circ_352018,RMVar_hsa_circ_164243,RMVar_hsa_circ_274860,RMVar_hsa_circ_164240,RMVar_hsa_circ_295062,RMVar_hsa_circ_164244,RMVar_hsa_circ_121605,RMVar_hsa_circ_119458,RMVar_hsa_circ_164245,RMVar_hsa_circ_164246,RMVar_hsa_circ_164247 50854 RMVar_ID_50854 Human_SNP_ID_542056006 A-to-I Human chr13 + 97349527 97349527 97349527 ACTAAGAACACATTTTTCCACAAAATTTGTTTATTTATTTGTTTTTTGAGACAGAGTCTTGCTCT ACTAAGAACACATTTTTCCACAAAATTTGTTTGTTTATTTGTTTTTTGAGACAGAGTCTTGCTCT A G MBNL2 Ensembl:ENSG00000139793 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1473811110 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12264266 RMVar_hsa_circ_112135,RMVar_hsa_circ_105674,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_371028,RMVar_hsa_circ_115054,RMVar_hsa_circ_164238,RMVar_hsa_circ_164239,RMVar_hsa_circ_164237,RMVar_hsa_circ_352018,RMVar_hsa_circ_164243,RMVar_hsa_circ_274860,RMVar_hsa_circ_164240,RMVar_hsa_circ_295062,RMVar_hsa_circ_164244,RMVar_hsa_circ_121605,RMVar_hsa_circ_119458,RMVar_hsa_circ_164245,RMVar_hsa_circ_164246,RMVar_hsa_circ_164247 50855 RMVar_ID_50855 Human_SNP_ID_542056507 A-to-I Human chr13 + 97351766 97351766 97351766 TAGGTTTTCGGCCAGCGTGGTAGCTCATGCCTATAATCCCAGCACTTTGCGGGGCAGAGGTGGGT TAGGTTTTCGGCCAGCGTGGTAGCTCATGCCTCTAATCCCAGCACTTTGCGGGGCAGAGGTGGGT A C MBNL2 Ensembl:ENSG00000139793 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1254879792 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2400822,Human_RBP_ID_23226168 RMVar_hsa_circ_112135,RMVar_hsa_circ_105674,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_371028,RMVar_hsa_circ_115054,RMVar_hsa_circ_164238,RMVar_hsa_circ_164239,RMVar_hsa_circ_164237,RMVar_hsa_circ_352018,RMVar_hsa_circ_164243,RMVar_hsa_circ_274860,RMVar_hsa_circ_164240,RMVar_hsa_circ_295062,RMVar_hsa_circ_164244,RMVar_hsa_circ_121605,RMVar_hsa_circ_119458,RMVar_hsa_circ_164245,RMVar_hsa_circ_164246,RMVar_hsa_circ_164247 50856 RMVar_ID_50856 Human_SNP_ID_542064992 A-to-I Human chr13 + 97389607 97389607 97389607 GCGTGGTTGTAGTCCCAGCTACTCAGGAGGCTAAAGTGGGAGGATTGCTTGAGGCCAGGAATTCA GCGTGGTTGTAGTCCCAGCTACTCAGGAGGCTTAAGTGGGAGGATTGCTTGAGGCCAGGAATTCA A T MBNL2 Ensembl:ENSG00000139793 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1477810681 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120088,RMVar_hsa_circ_164235,RMVar_hsa_circ_115054,RMVar_hsa_circ_164239,RMVar_hsa_circ_125512,RMVar_hsa_circ_164249,RMVar_hsa_circ_106831,RMVar_hsa_circ_164252 50857 RMVar_ID_50857 Human_SNP_ID_542214754 A-to-I Human chr13 + 97994987 97994987 97994987 TTCTCTGCCAAAAATACAAAAATTAGTCGGGCATGGTGGCACACGCCTGTGGTTCCAGCTACTCA TTCTCTGCCAAAAATACAAAAATTAGTCGGGCGTGGTGGCACACGCCTGTGGTTCCAGCTACTCA A G IPO5 Ensembl:ENSG00000065150 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1228476808 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12247945 RMVar_hsa_circ_113948,RMVar_hsa_circ_89995,RMVar_hsa_circ_164257,RMVar_hsa_circ_164258,RMVar_hsa_circ_372651,RMVar_hsa_circ_51899,RMVar_hsa_circ_86408,RMVar_hsa_circ_3996,RMVar_hsa_circ_164262,RMVar_hsa_circ_91206,RMVar_hsa_circ_164263,RMVar_hsa_circ_107629,RMVar_hsa_circ_116993,RMVar_hsa_circ_164266,RMVar_hsa_circ_164265,RMVar_hsa_circ_39029,RMVar_hsa_circ_305160,RMVar_hsa_circ_371626,RMVar_hsa_circ_164268,RMVar_hsa_circ_365796,RMVar_hsa_circ_292836,RMVar_hsa_circ_300223,RMVar_hsa_circ_164271,RMVar_hsa_circ_164272,RMVar_hsa_circ_164270 50858 RMVar_ID_50858 Human_SNP_ID_542215135 A-to-I Human chr13 + 97996136 97996136 97996136 TTAAGATGGGGTCTTGCTCTGTCATCCAGGCTAGAGTGCAGTGACATGATCTCAGCTCACTGCAG TTAAGATGGGGTCTTGCTCTGTCATCCAGGCTGGAGTGCAGTGACATGATCTCAGCTCACTGCAG A G IPO5 Ensembl:ENSG00000065150 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1434820800 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_113948,RMVar_hsa_circ_89995,RMVar_hsa_circ_164257,RMVar_hsa_circ_164258,RMVar_hsa_circ_372651,RMVar_hsa_circ_51899,RMVar_hsa_circ_86408,RMVar_hsa_circ_3996,RMVar_hsa_circ_164262,RMVar_hsa_circ_91206,RMVar_hsa_circ_164263,RMVar_hsa_circ_107629,RMVar_hsa_circ_116993,RMVar_hsa_circ_164266,RMVar_hsa_circ_164265,RMVar_hsa_circ_39029,RMVar_hsa_circ_305160,RMVar_hsa_circ_371626,RMVar_hsa_circ_164268,RMVar_hsa_circ_365796,RMVar_hsa_circ_292836,RMVar_hsa_circ_300223,RMVar_hsa_circ_164271,RMVar_hsa_circ_164272,RMVar_hsa_circ_164270 50859 RMVar_ID_50859 Human_SNP_ID_542215950 A-to-I Human chr13 + 97999084 97999084 97999084 AGAATCTCTTGAACCTGGGAGGTGGAGGTTGCAGTGAGCTGAGATCACGTCATTGCGCTACAGCC AGAATCTCTTGAACCTGGGAGGTGGAGGTTGCGGTGAGCTGAGATCACGTCATTGCGCTACAGCC A G IPO5 Ensembl:ENSG00000065150 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048388809 Functional Loss SNV dbSNP153 33..33 33 - - - 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_164274,RMVar_hsa_circ_50849,RMVar_hsa_circ_39029,RMVar_hsa_circ_305160,RMVar_hsa_circ_371626,RMVar_hsa_circ_164268,RMVar_hsa_circ_365796,RMVar_hsa_circ_292836,RMVar_hsa_circ_300223,RMVar_hsa_circ_164271,RMVar_hsa_circ_164272,RMVar_hsa_circ_164270,RMVar_hsa_circ_335542,RMVar_hsa_circ_85886,RMVar_hsa_circ_7556,RMVar_hsa_circ_12219,RMVar_hsa_circ_164275 50860 RMVar_ID_50860 Human_SNP_ID_542222702 A-to-I Human chr13 - 98024067 98024067 98024067 GTTACAAAATTCCCAGAAAACGTAAGAGCCACACACATTTTTCCCCTCCAGAAATAGCTTGCATT GTTACAAAATTCCCAGAAAACGTAAGAGCCACCCACATTTTTCCCCTCCAGAAATAGCTTGCATT T G lnc-RNF113B-2 RNACentral:URS00008BA22B lincRNA exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1228076965 Functional Loss SNV dbSNP153 33..33 33 - - - 50861 RMVar_ID_50861 Human_SNP_ID_542261419 A-to-I Human chr13 + 98178376 98178376 98178376 TGCCACCACACCCAGCTAACTTCTGTGTTTTTAGTAGCGACAGGGTTTCACCATGTTGGCCAGGC TGCCACCACACCCAGCTAACTTCTGTGTTTTTCGTAGCGACAGGGTTTCACCATGTTGGCCAGGC A C FARP1 Ensembl:ENSG00000152767 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1406845603 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_164286 50862 RMVar_ID_50862 Human_SNP_ID_542263444 A-to-I Human chr13 + 98186336 98186336 98186336 CTCCATGTTGATCAGGCTGATCTTGAACTCCCAACTTCAGGTGATCCACCCACCTCGACCTCCCA CTCCATGTTGATCAGGCTGATCTTGAACTCCCGACTTCAGGTGATCCACCCACCTCGACCTCCCA A G FARP1 Ensembl:ENSG00000152767 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1566716891 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_164286 50863 RMVar_ID_50863 Human_SNP_ID_542272388 A-to-I Human chr13 + 98222761 98222761 98222761 CTCCTGCCTCAGCCTCCCCAGTAGGTAGGACTAGGACTGCAGGCGTGCACCACCATGCCCAGCTA CTCCTGCCTCAGCCTCCCCAGTAGGTAGGACTGGGACTGCAGGCGTGCACCACCATGCCCAGCTA A G FARP1 Ensembl:ENSG00000152767 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1441221425 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_164291,RMVar_hsa_circ_36662,RMVar_hsa_circ_164290,RMVar_hsa_circ_164288 50864 RMVar_ID_50864 Human_SNP_ID_542305626 A-to-I Human chr13 + 98353241 98353241 98353241 CAGACTTATGCAGTTACGATGAAACTCTGCATAGTGGTTACCTGTAGAGGGCGGGAGTTCAGTTT CAGACTTATGCAGTTACGATGAAACTCTGCATCGTGGTTACCTGTAGAGGGCGGGAGTTCAGTTT A C FARP1 Ensembl:ENSG00000152767 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1351267544 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17562077 RMVar_hsa_circ_164287,RMVar_hsa_circ_54973,RMVar_hsa_circ_282225,RMVar_hsa_circ_312229,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_273672,RMVar_hsa_circ_21852,RMVar_hsa_circ_351099,RMVar_hsa_circ_328962,RMVar_hsa_circ_73722,RMVar_hsa_circ_78761,RMVar_hsa_circ_72738,RMVar_hsa_circ_164300,RMVar_hsa_circ_164301 50865 RMVar_ID_50865 Human_SNP_ID_542315706 A-to-I Human chr13 + 98392289 98392286 98392290 GGTGGATCACTTGAGCTCAGGAGTTTGAGACCAGCCTGGGTAACATGACGAAAGCTCATCTCTAC GGTGGATCACTTGAGCTCAGGAGTTTGAGA____CCTGGGTAACATGACGAAAGCTCATCTCTAC ACCAG A FARP1 Ensembl:ENSG00000152767 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs529088129 Functional Loss DEL dbSNP153 31..34 33 - - - RMVar_hsa_circ_164287,RMVar_hsa_circ_54973,RMVar_hsa_circ_82445,RMVar_hsa_circ_36662,RMVar_hsa_circ_71159,RMVar_hsa_circ_351099,RMVar_hsa_circ_73722,RMVar_hsa_circ_78761,RMVar_hsa_circ_164301,RMVar_hsa_circ_267581,RMVar_hsa_circ_39169,RMVar_hsa_circ_40368,RMVar_hsa_circ_2966,RMVar_hsa_circ_49038,RMVar_hsa_circ_319211,RMVar_hsa_circ_359184,RMVar_hsa_circ_339003,RMVar_hsa_circ_277511,RMVar_hsa_circ_31541,RMVar_hsa_circ_164308,RMVar_hsa_circ_164309,RMVar_hsa_circ_164310,RMVar_hsa_circ_266372,RMVar_hsa_circ_267464,RMVar_hsa_circ_164311,RMVar_hsa_circ_267028,RMVar_hsa_circ_62436,RMVar_hsa_circ_107526,RMVar_hsa_circ_164313,RMVar_hsa_circ_55332 50866 RMVar_ID_50866 Human_SNP_ID_542357657 A-to-I Human chr13 - 98547426 98547426 98547426 CTCACGCCACAGCCTCCCGAGTAGCTGGGACTATAGGCGTGTGCCACCGTGCCCGGCTCATTGTT CTCACGCCACAGCCTCCCGAGTAGCTGGGACTGTAGGCGTGTGCCACCGTGCCCGGCTCATTGTT T C STK24 Ensembl:ENSG00000102572 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs369608682 Functional Loss SNV dbSNP153 33..33 33 - - - 50867 RMVar_ID_50867 Human_SNP_ID_542479829 A-to-I Human chr13 - 99049777 99049777 99049777 GTGGTTGCTCATTCCTGTAATCCCAACACTTTAGGAGACTGAGGTGGGAGTATCTTTTGAGTCCA GTGGTTGCTCATTCCTGTAATCCCAACACTTTGGGAGACTGAGGTGGGAGTATCTTTTGAGTCCA T C DOCK9 Ensembl:ENSG00000088387 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1368118512 Functional Loss SNV dbSNP153 33..33 33 - - - 50868 RMVar_ID_50868 Human_SNP_ID_542485206 A-to-I Human chr13 - 99072912 99072912 99072912 TCACTGAAGCCTTGACCTCCCGGGCTCAAGCAATCCTCCCATCTTCAGCCTTGCAAGTAGCTGGG TCACTGAAGCCTTGACCTCCCGGGCTCAAGCAGTCCTCCCATCTTCAGCCTTGCAAGTAGCTGGG T C DOCK9 Ensembl:ENSG00000088387 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs537920714 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_230564 50869 RMVar_ID_50869 Human_SNP_ID_542485875 A-to-I Human chr13 - 99075492 99075492 99075492 AAAATTAGCTGGGCTTGGTGGCACACACCTGTAGTCCCTAGCTACTCAGGAGGCTGAGATGGCAG AAAATTAGCTGGGCTTGGTGGCACACACCTGTGGTCCCTAGCTACTCAGGAGGCTGAGATGGCAG T C DOCK9 Ensembl:ENSG00000088387 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1347115339 Functional Loss SNV dbSNP153 33..33 33 - - - 50870 RMVar_ID_50870 Human_SNP_ID_542518571 A-to-I Human chr13 + 99203210 99203210 99203210 AGGTGCCCACCATCACACCTGGCTATTTTTGTATTTTTAGTAGAGACGGGGTTTTGCCATGTTGA AGGTGCCCACCATCACACCTGGCTATTTTTGTGTTTTTAGTAGAGACGGGGTTTTGCCATGTTGA A G UBAC2 Ensembl:ENSG00000134882 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335962741 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24041,RMVar_hsa_circ_82397,RMVar_hsa_circ_323112,RMVar_hsa_circ_164376,RMVar_hsa_circ_331666,RMVar_hsa_circ_61741 50871 RMVar_ID_50871 Human_SNP_ID_542529809 A-to-I Human chr13 + 99245767 99245767 99245767 TGAGGCAGAAGAATCACTTGAACCCGGGAGGCAGAGGTTGCAGTGAGCGGAGATCGCTCCACTGC TGAGGCAGAAGAATCACTTGAACCCGGGAGGCGGAGGTTGCAGTGAGCGGAGATCGCTCCACTGC A G UBAC2 Ensembl:ENSG00000134882 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1252121399 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_24041,RMVar_hsa_circ_82397,RMVar_hsa_circ_164376,RMVar_hsa_circ_331666,RMVar_hsa_circ_71441,RMVar_hsa_circ_348036,RMVar_hsa_circ_284102,RMVar_hsa_circ_75048,RMVar_hsa_circ_164379,RMVar_hsa_circ_317804,RMVar_hsa_circ_164381 50872 RMVar_ID_50872 Human_SNP_ID_542537057 A-to-I Human chr13 + 99274892 99274892 99274892 GGTGCGCACCACCACTCCCAGCTAATTTTTGTATTCTTTGTAGAGATGAGGTTTCTCCATGTTGC GGTGCGCACCACCACTCCCAGCTAATTTTTGTGTTCTTTGTAGAGATGAGGTTTCTCCATGTTGC A G UBAC2 Ensembl:ENSG00000134882 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1474118707 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12252911 RMVar_hsa_circ_24041,RMVar_hsa_circ_82397,RMVar_hsa_circ_164376,RMVar_hsa_circ_331666,RMVar_hsa_circ_71441,RMVar_hsa_circ_348036,RMVar_hsa_circ_284102,RMVar_hsa_circ_75048,RMVar_hsa_circ_164379,RMVar_hsa_circ_317804,RMVar_hsa_circ_164381 50873 RMVar_ID_50873 Human_SNP_ID_542541814 A-to-I Human chr13 - 99295066 99295066 99295066 CAGATGATGATACATTCCAAGTCTTCAAATGGAAAGTGAAATGGATTGTATTTTGGTTTATAGTG CAGATGATGATACATTCCAAGTCTTCAAATGGTAAGTGAAATGGATTGTATTTTGGTTTATAGTG T A GPR183 Ensembl:ENSG00000169508 Protein coding CDS GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1177969574 Functional Loss SNV dbSNP153 33..33 33 - - - 50874 RMVar_ID_50874 Human_SNP_ID_542563619 A-to-I Human chr13 + 99383269 99383269 99383269 TCAGGAATTTTCACATAAAATGCTCTCGAGTCAGGTCTCTCAAATCCTGCCTGACCTTTTAAGTC TCAGGAATTTTCACATAAAATGCTCTCGAGTCCGGTCTCTCAAATCCTGCCTGACCTTTTAAGTC A C UBAC2 Ensembl:ENSG00000134882 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs373815033 Functional Loss SNV dbSNP153 33..33 33 - - - 50875 RMVar_ID_50875 Human_SNP_ID_542563622 A-to-I Human chr13 + 99383278 99383278 99383278 TTCACATAAAATGCTCTCGAGTCAGGTCTCTCAAATCCTGCCTGACCTTTTAAGTCTAGGACAGT TTCACATAAAATGCTCTCGAGTCAGGTCTCTCGAATCCTGCCTGACCTTTTAAGTCTAGGACAGT A G UBAC2 Ensembl:ENSG00000134882 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1338898149 Functional Loss SNV dbSNP153 33..33 33 - - - 50876 RMVar_ID_50876 Human_SNP_ID_542606580 A-to-I Human chr13 + 99544237 99544237 99544237 GGGCATGGTGGCAGGTGCCTGTAATCCCAGCTACTTGTGGGGCTGAGGCAGTAGCTTGAACCTGG GGGCATGGTGGCAGGTGCCTGTAATCCCAGCTGCTTGTGGGGCTGAGGCAGTAGCTTGAACCTGG A G TM9SF2 Ensembl:ENSG00000125304 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1310127782 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17686,RMVar_hsa_circ_127100,RMVar_hsa_circ_121233,RMVar_hsa_circ_91100,RMVar_hsa_circ_128127,RMVar_hsa_circ_164387,RMVar_hsa_circ_164388,RMVar_hsa_circ_164386,RMVar_hsa_circ_81449,RMVar_hsa_circ_85023,RMVar_hsa_circ_164399,RMVar_hsa_circ_164394,RMVar_hsa_circ_164395,RMVar_hsa_circ_164393,RMVar_hsa_circ_329697,RMVar_hsa_circ_272826,RMVar_hsa_circ_164400,RMVar_hsa_circ_337805,RMVar_hsa_circ_41109,RMVar_hsa_circ_358356,RMVar_hsa_circ_164401,RMVar_hsa_circ_314234,RMVar_hsa_circ_272330,RMVar_hsa_circ_164406,RMVar_hsa_circ_164407,RMVar_hsa_circ_372392,RMVar_hsa_circ_122915,RMVar_hsa_circ_164408,RMVar_hsa_circ_164409,RMVar_hsa_circ_62348,RMVar_hsa_circ_164410,RMVar_hsa_circ_119514,RMVar_hsa_circ_358900 50877 RMVar_ID_50877 Human_SNP_ID_542606601 A-to-I Human chr13 + 99544323 99544323 99544323 TGAGATTGCGCCACTGCACTCCAGCCTGGGTGACAGTGCAAGACTCCATCTCAAAAAAAAAAACA TGAGATTGCGCCACTGCACTCCAGCCTGGGTGGCAGTGCAAGACTCCATCTCAAAAAAAAAAACA A G TM9SF2 Ensembl:ENSG00000125304 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1476092551 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17686,RMVar_hsa_circ_127100,RMVar_hsa_circ_121233,RMVar_hsa_circ_91100,RMVar_hsa_circ_128127,RMVar_hsa_circ_164387,RMVar_hsa_circ_164388,RMVar_hsa_circ_164386,RMVar_hsa_circ_81449,RMVar_hsa_circ_85023,RMVar_hsa_circ_164399,RMVar_hsa_circ_164394,RMVar_hsa_circ_164395,RMVar_hsa_circ_164393,RMVar_hsa_circ_329697,RMVar_hsa_circ_272826,RMVar_hsa_circ_164400,RMVar_hsa_circ_337805,RMVar_hsa_circ_41109,RMVar_hsa_circ_358356,RMVar_hsa_circ_164401,RMVar_hsa_circ_314234,RMVar_hsa_circ_272330,RMVar_hsa_circ_164406,RMVar_hsa_circ_164407,RMVar_hsa_circ_372392,RMVar_hsa_circ_122915,RMVar_hsa_circ_164408,RMVar_hsa_circ_164409,RMVar_hsa_circ_62348,RMVar_hsa_circ_164410,RMVar_hsa_circ_119514,RMVar_hsa_circ_358900 50878 RMVar_ID_50878 Human_SNP_ID_542606603 A-to-I Human chr13 + 99544330 99544330 99544330 GCGCCACTGCACTCCAGCCTGGGTGACAGTGCAAGACTCCATCTCAAAAAAAAAAACAAAAAACA GCGCCACTGCACTCCAGCCTGGGTGACAGTGCGAGACTCCATCTCAAAAAAAAAAACAAAAAACA A G TM9SF2 Ensembl:ENSG00000125304 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs941991706 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17686,RMVar_hsa_circ_127100,RMVar_hsa_circ_121233,RMVar_hsa_circ_91100,RMVar_hsa_circ_128127,RMVar_hsa_circ_164387,RMVar_hsa_circ_164388,RMVar_hsa_circ_164386,RMVar_hsa_circ_81449,RMVar_hsa_circ_85023,RMVar_hsa_circ_164399,RMVar_hsa_circ_164394,RMVar_hsa_circ_164395,RMVar_hsa_circ_164393,RMVar_hsa_circ_329697,RMVar_hsa_circ_272826,RMVar_hsa_circ_164400,RMVar_hsa_circ_337805,RMVar_hsa_circ_41109,RMVar_hsa_circ_358356,RMVar_hsa_circ_164401,RMVar_hsa_circ_314234,RMVar_hsa_circ_272330,RMVar_hsa_circ_164406,RMVar_hsa_circ_164407,RMVar_hsa_circ_372392,RMVar_hsa_circ_122915,RMVar_hsa_circ_164408,RMVar_hsa_circ_164409,RMVar_hsa_circ_62348,RMVar_hsa_circ_164410,RMVar_hsa_circ_119514,RMVar_hsa_circ_358900 50879 RMVar_ID_50879 Human_SNP_ID_542629739 A-to-I Human chr13 + 99636938 99636938 99636938 ACTCTCTCGCCCAGGTCGGAGTGCAGTGGTGCAGTCTTGGCTCACTGCATCACTGCATCCCCCAG ACTCTCTCGCCCAGGTCGGAGTGCAGTGGTGCGGTCTTGGCTCACTGCATCACTGCATCCCCCAG A G CLYBL Ensembl:ENSG00000125246 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1351600778 Functional Loss SNV dbSNP153 33..33 33 - - - 50880 RMVar_ID_50880 Human_SNP_ID_542649014 A-to-I Human chr13 + 99715634 99715634 99715634 CACCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGTATGAATCACTACACCCGGCCTGTACGG CACCCGCCTTGGCCTCCCAAAGTGCTGGGATTGCAGGTATGAATCACTACACCCGGCCTGTACGG A G CLYBL Ensembl:ENSG00000125246 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1035198793 Functional Loss SNV dbSNP153 33..33 33 - - - 50881 RMVar_ID_50881 Human_SNP_ID_542740040 A-to-I Human chr13 - 100070078 100070078 100070078 ACTCAAACGCCCCAGTTCAAATGACCCACCTCAGCCTCCAAGTAGCTGGGACTACAGGCATGCGC ACTCAAACGCCCCAGTTCAAATGACCCACCTCGGCCTCCAAGTAGCTGGGACTACAGGCATGCGC T C PCCA-DT Ensembl:ENSG00000274605 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs182408388 Functional Loss SNV dbSNP153 33..33 33 - - - 50882 RMVar_ID_50882 Human_SNP_ID_542741044 A-to-I Human chr13 - 100073860 100073860 100073860 CTGAGGTCAGGAGTTCGAGAGCAGCCTGGCCAACGTGGTGAAAACCCATCTCTACTAAAAATACA CTGAGGTCAGGAGTTCGAGAGCAGCCTGGCCACCGTGGTGAAAACCCATCTCTACTAAAAATACA T G PCCA-DT Ensembl:ENSG00000274605 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs558528468 Functional Loss SNV dbSNP153 33..33 33 - - - 50883 RMVar_ID_50883 Human_SNP_ID_542741518 A-to-I Human chr13 - 100075552 100075551 100075552 CCGTCGGCCTCCCGGACTCAAGTGATCCTCCCACCTCAGCCCCCCAAGTAGCTGGGACTACAGGC CCGTCGGCCTCCCGGACTCAAGTGATCCTCCC_CCTCAGCCCCCCAAGTAGCTGGGACTACAGGC GT G PCCA-DT Ensembl:ENSG00000274605 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1342450696 Functional Loss DEL dbSNP153 33..33 33 - - - 50884 RMVar_ID_50884 Human_SNP_ID_542787218 A-to-I Human chr13 + 100260536 100260536 100260536 CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCGCACACTGCCACGCCTGGCTAATTTTT CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTGCAGGCGCACACTGCCACGCCTGGCTAATTTTT A G PCCA Ensembl:ENSG00000175198 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs531236605 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_4310,RMVar_hsa_circ_115204,RMVar_hsa_circ_54866,RMVar_hsa_circ_55134,RMVar_hsa_circ_62279,RMVar_hsa_circ_164425,RMVar_hsa_circ_114098,RMVar_hsa_circ_57427,RMVar_hsa_circ_118769,RMVar_hsa_circ_164428,RMVar_hsa_circ_117948,RMVar_hsa_circ_164430,RMVar_hsa_circ_164431,RMVar_hsa_circ_349982,RMVar_hsa_circ_367331,RMVar_hsa_circ_373074,RMVar_hsa_circ_69165,RMVar_hsa_circ_75069,RMVar_hsa_circ_61650,RMVar_hsa_circ_18292,RMVar_hsa_circ_95331,RMVar_hsa_circ_313565,RMVar_hsa_circ_164434,RMVar_hsa_circ_353634,RMVar_hsa_circ_367905,RMVar_hsa_circ_359303,RMVar_hsa_circ_349994,RMVar_hsa_circ_304524,RMVar_hsa_circ_288208,RMVar_hsa_circ_17097,RMVar_hsa_circ_57282,RMVar_hsa_circ_66713,RMVar_hsa_circ_33549,RMVar_hsa_circ_164435,RMVar_hsa_circ_164437,RMVar_hsa_circ_164436,RMVar_hsa_circ_355048,RMVar_hsa_circ_356734,RMVar_hsa_circ_112364,RMVar_hsa_circ_164442,RMVar_hsa_circ_57613,RMVar_hsa_circ_71331,RMVar_hsa_circ_21385,RMVar_hsa_circ_164443,RMVar_hsa_circ_295296,RMVar_hsa_circ_343735,RMVar_hsa_circ_164441,RMVar_hsa_circ_347222,RMVar_hsa_circ_355986,RMVar_hsa_circ_303785,RMVar_hsa_circ_336306,RMVar_hsa_circ_296334,RMVar_hsa_circ_276484,RMVar_hsa_circ_293835,RMVar_hsa_circ_273212,RMVar_hsa_circ_164445,RMVar_hsa_circ_164447,RMVar_hsa_circ_164448,RMVar_hsa_circ_164449,RMVar_hsa_circ_164446 50885 RMVar_ID_50885 Human_SNP_ID_542837786 A-to-I Human chr13 + 100467577 100467577 100467577 TATTTTTAGTAGACACGGGGTTTCACCCTGTTAGCCAGGATCGTCTTGATCTCCTGACCTCATGA TATTTTTAGTAGACACGGGGTTTCACCCTGTTCGCCAGGATCGTCTTGATCTCCTGACCTCATGA A C PCCA Ensembl:ENSG00000175198 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1366836180 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 50886 RMVar_ID_50886 Human_SNP_ID_542842686 A-to-I Human chr13 + 100488361 100488361 100488361 GTGATCCACCCGCCTCGGCTTCCCAAAGTGCTAGGATTTACAGGTGTGAGCCGGCCGACCCTATA GTGATCCACCCGCCTCGGCTTCCCAAAGTGCTGGGATTTACAGGTGTGAGCCGGCCGACCCTATA A G PCCA Ensembl:ENSG00000175198 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215850816 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 50887 RMVar_ID_50887 Human_SNP_ID_542863794 A-to-I Human chr13 - 100572586 100572586 100572586 TAGCCACTGCACCCCAGCCTGGGCAACATAGCAAGACCCTGTCTACAAAAATAAATAAATGTTTT TAGCCACTGCACCCCAGCCTGGGCAACATAGCGAGACCCTGTCTACAAAAATAAATAAATGTTTT T C AL356966.1,GGACT Ensembl:ENSG00000224356,Ensembl:ENSG00000134864 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs377461745 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_118471 50888 RMVar_ID_50888 Human_SNP_ID_542876502 A-to-I Human chr13 - 100623262 100623262 100623262 CGGCACTGCACTCCAGCCTGGGCAACAGAGTGAGATTCTGCCTCAAAAAAATTAAGTAAGTAAAA CGGCACTGCACTCCAGCCTGGGCAACAGAGTGGGATTCTGCCTCAAAAAAATTAAGTAAGTAAAA T C TMTC4 Ensembl:ENSG00000125247 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1419351805 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1780,RMVar_hsa_circ_126322,RMVar_hsa_circ_31365,RMVar_hsa_circ_164495 50889 RMVar_ID_50889 Human_SNP_ID_542876523 A-to-I Human chr13 - 100623318 100623318 100623318 TGAGGCAGGAAAATCACTTGAACCTGGGAAGCAGAGGTTGCAGTGAGCCAAGATTGCGGCACTGC TGAGGCAGGAAAATCACTTGAACCTGGGAAGCTGAGGTTGCAGTGAGCCAAGATTGCGGCACTGC T A TMTC4 Ensembl:ENSG00000125247 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1460983554 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1780,RMVar_hsa_circ_126322,RMVar_hsa_circ_31365,RMVar_hsa_circ_164495 50890 RMVar_ID_50890 Human_SNP_ID_542876534 A-to-I Human chr13 - 100623370 100623370 100623370 AAAATAGCCAGACATGGTGGTACGTGCCTGTAATCCCAGCTGCTGGGGAGGCTGAGGCAGGAAAA AAAATAGCCAGACATGGTGGTACGTGCCTGTATTCCCAGCTGCTGGGGAGGCTGAGGCAGGAAAA T A TMTC4 Ensembl:ENSG00000125247 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs943923712 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1780,RMVar_hsa_circ_126322,RMVar_hsa_circ_31365,RMVar_hsa_circ_164495 50891 RMVar_ID_50891 Human_SNP_ID_542876535 A-to-I Human chr13 - 100623370 100623370 100623370 AAAATAGCCAGACATGGTGGTACGTGCCTGTAATCCCAGCTGCTGGGGAGGCTGAGGCAGGAAAA AAAATAGCCAGACATGGTGGTACGTGCCTGTAGTCCCAGCTGCTGGGGAGGCTGAGGCAGGAAAA T C TMTC4 Ensembl:ENSG00000125247 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs943923712 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1780,RMVar_hsa_circ_126322,RMVar_hsa_circ_31365,RMVar_hsa_circ_164495 50892 RMVar_ID_50892 Human_SNP_ID_542876547 A-to-I Human chr13 - 100623402 100623402 100623402 ATGGCGAAACCACATCTCTACTAAAAATACAAAAAATAGCCAGACATGGTGGTACGTGCCTGTAA ATGGCGAAACCACATCTCTACTAAAAATACAAGAAATAGCCAGACATGGTGGTACGTGCCTGTAA T C TMTC4 Ensembl:ENSG00000125247 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs971837946 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1780,RMVar_hsa_circ_126322,RMVar_hsa_circ_31365,RMVar_hsa_circ_164495 50893 RMVar_ID_50893 Human_SNP_ID_542876768 A-to-I Human chr13 - 100623971 100623971 100623971 TAGAGATGGAGGTCATGATGACTGCAAGGAAGAGACTGGACCCATACAATGTACTACCCCCAAAG TAGAGATGGAGGTCATGATGACTGCAAGGAAGGGACTGGACCCATACAATGTACTACCCCCAAAG T C COX5BP6,TMTC4 Ensembl:ENSG00000237082,Ensembl:ENSG00000125247 Pseudogene,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1406484800 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5246601 RMVar_hsa_circ_1780,RMVar_hsa_circ_126322,RMVar_hsa_circ_31365,RMVar_hsa_circ_164495 50894 RMVar_ID_50894 Human_SNP_ID_542876806 A-to-I Human chr13 - 100624137 100624137 100624137 TATTTTTAGTAGAGACGGGATTTCACCATGTTAGCCAGGATGGTCTAGATCTCCTGACCTCGTGA TATTTTTAGTAGAGACGGGATTTCACCATGTTTGCCAGGATGGTCTAGATCTCCTGACCTCGTGA T A COX5BP6,TMTC4 Ensembl:ENSG00000237082,Ensembl:ENSG00000125247 Pseudogene,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1213849587 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1780,RMVar_hsa_circ_126322,RMVar_hsa_circ_31365,RMVar_hsa_circ_164495 50895 RMVar_ID_50895 Human_SNP_ID_542876807 A-to-I Human chr13 - 100624137 100624137 100624137 TATTTTTAGTAGAGACGGGATTTCACCATGTTAGCCAGGATGGTCTAGATCTCCTGACCTCGTGA TATTTTTAGTAGAGACGGGATTTCACCATGTTGGCCAGGATGGTCTAGATCTCCTGACCTCGTGA T C COX5BP6,TMTC4 Ensembl:ENSG00000237082,Ensembl:ENSG00000125247 Pseudogene,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1213849587 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1780,RMVar_hsa_circ_126322,RMVar_hsa_circ_31365,RMVar_hsa_circ_164495 50896 RMVar_ID_50896 Human_SNP_ID_542876826 A-to-I Human chr13 - 100624204 100624204 100624204 CTTCTGCCTCAGCCTCCGGAGTAGCTGGGACTATAGGCGCCCGCCACCATGCCTGGCTAATGTTT CTTCTGCCTCAGCCTCCGGAGTAGCTGGGACTGTAGGCGCCCGCCACCATGCCTGGCTAATGTTT T C COX5BP6,TMTC4 Ensembl:ENSG00000237082,Ensembl:ENSG00000125247 Pseudogene,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025436588 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1780,RMVar_hsa_circ_126322,RMVar_hsa_circ_31365,RMVar_hsa_circ_164495 50897 RMVar_ID_50897 Human_SNP_ID_542884297 A-to-I Human chr13 - 100652316 100652316 100652316 CACCACCACGCCCAGCTAGTTTTTGTGTTTTTAGTAGAGACGGGGTTTCGCCACATTGGCCAGGC CACCACCACGCCCAGCTAGTTTTTGTGTTTTTGGTAGAGACGGGGTTTCGCCACATTGGCCAGGC T C TMTC4 Ensembl:ENSG00000125247 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1444089153 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_117950 RMVar_hsa_circ_1780,RMVar_hsa_circ_31365,RMVar_hsa_circ_72017,RMVar_hsa_circ_319563,RMVar_hsa_circ_164500,RMVar_hsa_circ_102965,RMVar_hsa_circ_164501,RMVar_hsa_circ_306540,RMVar_hsa_circ_321181 50898 RMVar_ID_50898 Human_SNP_ID_542889055 A-to-I Human chr13 - 100670670 100670670 100670670 TGCTGGGATTACAGGCGTGAGCCATTGCAACCAGCCTTGATTTGTTGTTTTTTAAGTAGCAGGAG TGCTGGGATTACAGGCGTGAGCCATTGCAACCGGCCTTGATTTGTTGTTTTTTAAGTAGCAGGAG T C TMTC4 Ensembl:ENSG00000125247 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs887398943 Functional Loss SNV dbSNP153 33..33 33 - - - 50899 RMVar_ID_50899 Human_SNP_ID_543057836 A-to-I Human chr13 - 101347481 101347481 101347481 GCAAAGATGAATCATTTGGCCTACATGTAAGAATGAGAAATGGGGAGATATACACGATGTGTCTG GCAAAGATGAATCATTTGGCCTACATGTAAGATTGAGAAATGGGGAGATATACACGATGTGTCTG T A NALCN Ensembl:ENSG00000102452 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs529029849 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 50900 RMVar_ID_50900 Human_SNP_ID_543057837 A-to-I Human chr13 - 101347481 101347481 101347481 GCAAAGATGAATCATTTGGCCTACATGTAAGAATGAGAAATGGGGAGATATACACGATGTGTCTG GCAAAGATGAATCATTTGGCCTACATGTAAGAGTGAGAAATGGGGAGATATACACGATGTGTCTG T C NALCN Ensembl:ENSG00000102452 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs529029849 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 50901 RMVar_ID_50901 Human_SNP_ID_543064295 A-to-I Human chr13 - 101374386 101374385 101374387 CAGGAGGCACCTGTGATCGGGAGGCTGAGACAAGAGAATTGCTTGAATCCAGAAGGCGGAGGTTG CAGGAGGCACCTGTGATCGGGAGGCTGAGAC__GAGAATTGCTTGAATCCAGAAGGCGGAGGTTG CTT C NALCN Ensembl:ENSG00000102452 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1397087973 Functional Loss DEL dbSNP153 32..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 50902 RMVar_ID_50902 Human_SNP_ID_543213324 A-to-I Human chr13 - 101969374 101969374 101969374 TATTTTTAGTAGAGACGGGGATTCACCGTGTTAGCCAGGATGGTCTCGATCTCCTGACCTTGTGA TATTTTTAGTAGAGACGGGGATTCACCGTGTTGGCCAGGATGGTCTCGATCTCCTGACCTTGTGA T C FGF14 Ensembl:ENSG00000102466 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs553423801 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_280140 50903 RMVar_ID_50903 Human_SNP_ID_543239557 A-to-I Human chr13 - 102074155 102074155 102074155 ATTTTTTAAAATTGCCAGGTATGGTGGTGCACACTTGTAGTCCCACCTACTTGGAGGCTGAGGTG ATTTTTTAAAATTGCCAGGTATGGTGGTGCACGCTTGTAGTCCCACCTACTTGGAGGCTGAGGTG T C FGF14 Ensembl:ENSG00000102466 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs569470382 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_280140 50904 RMVar_ID_50904 Human_SNP_ID_543239558 A-to-I Human chr13 - 102074155 102074155 102074155 ATTTTTTAAAATTGCCAGGTATGGTGGTGCACACTTGTAGTCCCACCTACTTGGAGGCTGAGGTG ATTTTTTAAAATTGCCAGGTATGGTGGTGCACCCTTGTAGTCCCACCTACTTGGAGGCTGAGGTG T G FGF14 Ensembl:ENSG00000102466 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs569470382 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_280140 50905 RMVar_ID_50905 Human_SNP_ID_543246229 A-to-I Human chr13 - 102100991 102100991 102100991 GGGTTCCAGCAAATCTTCCGCCTCAGCCTCCCAAGTAACTGGGATTACAGGCACCCACCATCATG GGGTTCCAGCAAATCTTCCGCCTCAGCCTCCCGAGTAACTGGGATTACAGGCACCCACCATCATG T C FGF14 Ensembl:ENSG00000102466 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs914975423 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_280140 50906 RMVar_ID_50906 Human_SNP_ID_543252366 A-to-I Human chr13 - 102126342 102126338 102126342 ATGAACCTTGAAAACATTATGCTCAGTGAAATAAACCAGACACAATAGGACACATATTGTATGAT ATGAACCTTGAAAACATTATGCTCAGTGAAAT____CAGACACAATAGGACACATATTGTATGAT GGTTT G FGF14 Ensembl:ENSG00000102466 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1193261905 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_280140 50907 RMVar_ID_50907 Human_SNP_ID_543252366 A-to-I Human chr13 - 102126341 102126338 102126342 TGAACCTTGAAAACATTATGCTCAGTGAAATAAACCAGACACAATAGGACACATATTGTATGATT TGAACCTTGAAAACATTATGCTCAGTGAAAT____CAGACACAATAGGACACATATTGTATGATT GGTTT G FGF14 Ensembl:ENSG00000102466 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1193261905 Functional Loss DEL dbSNP153 32..35 33 - - - RMVar_hsa_circ_280140 50908 RMVar_ID_50908 Human_SNP_ID_543254543 A-to-I Human chr13 - 102134967 102134967 102134967 GTTACCCAGACTGGTCTTGAACTCCTAGACTCAAGCAATCCCTCTACTTCGGCCTCCCAGATTGC GTTACCCAGACTGGTCTTGAACTCCTAGACTCGAGCAATCCCTCTACTTCGGCCTCCCAGATTGC T C FGF14 Ensembl:ENSG00000102466 Protein coding intron GSE107867 ASD brains,frontal_cortex;ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1411166418 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23583610 RMVar_hsa_circ_280140 50909 RMVar_ID_50909 Human_SNP_ID_543254822 A-to-I Human chr13 - 102135906 102135906 102135906 CATGTCTATAATCCCAACACTTTGGGAGGCCAAGGTGAGTAGATCACTTGAGGTCAGGATTTAGA CATGTCTATAATCCCAACACTTTGGGAGGCCAGGGTGAGTAGATCACTTGAGGTCAGGATTTAGA T C FGF14 Ensembl:ENSG00000102466 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs555345351 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_280140 50910 RMVar_ID_50910 Human_SNP_ID_543255318 A-to-I Human chr13 - 102137811 102137811 102137811 ATGAGACCATCATTCTTTTCAGACAAAGCCTTACCCACTTGAAGGATGTGATCTAACTTATGGCC ATGAGACCATCATTCTTTTCAGACAAAGCCTTGCCCACTTGAAGGATGTGATCTAACTTATGGCC T C FGF14 Ensembl:ENSG00000102466 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs950096740 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_280140 50911 RMVar_ID_50911 Human_SNP_ID_543267115 A-to-I Human chr13 - 102182036 102182036 102182036 GAGTTAGTTTTCTAGGGCTGCCATAACAAAGTACCACAAAATGGGTGGCTGAAAACAACGGCAAT GAGTTAGTTTTCTAGGGCTGCCATAACAAAGTGCCACAAAATGGGTGGCTGAAAACAACGGCAAT T C FGF14 Ensembl:ENSG00000102466 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs558503859 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_280140 50912 RMVar_ID_50912 Human_SNP_ID_543270620 A-to-I Human chr13 - 102197312 102197312 102197312 GGGCAGTAGTACTTGGTGCTGGTAAAGGGGTTAGGCTCTGGGTCTTGAAATTGTTTCCTACTCAT GGGCAGTAGTACTTGGTGCTGGTAAAGGGGTTGGGCTCTGGGTCTTGAAATTGTTTCCTACTCAT T C FGF14 Ensembl:ENSG00000102466 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1474620834 Functional Loss SNV dbSNP153 33..33 33 - - - 50913 RMVar_ID_50913 Human_SNP_ID_543271473 A-to-I Human chr13 - 102200913 102200913 102200913 TGTTTTTAGTAGAGACGGGGTTTCACCATGTTAGCCAAGATGGTCTCGATCTCCCGACCTCATGA TGTTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAAGATGGTCTCGATCTCCCGACCTCATGA T C FGF14 Ensembl:ENSG00000102466 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs566287888 Functional Loss SNV dbSNP153 33..33 33 - - - 50914 RMVar_ID_50914 Human_SNP_ID_543271548 A-to-I Human chr13 - 102201074 102201074 102201074 TTTTGAGAGACGGAGTCTCGCTCTGTCGCCCAAGCTGGAGTGCAGTGGCGCGATCTCAGCTCAAG TTTTGAGAGACGGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCGATCTCAGCTCAAG T C FGF14 Ensembl:ENSG00000102466 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs987338923 Functional Loss SNV dbSNP153 33..33 33 - - - 50915 RMVar_ID_50915 Human_SNP_ID_543271549 A-to-I Human chr13 - 102201074 102201074 102201074 TTTTGAGAGACGGAGTCTCGCTCTGTCGCCCAAGCTGGAGTGCAGTGGCGCGATCTCAGCTCAAG TTTTGAGAGACGGAGTCTCGCTCTGTCGCCCACGCTGGAGTGCAGTGGCGCGATCTCAGCTCAAG T G FGF14 Ensembl:ENSG00000102466 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs987338923 Functional Loss SNV dbSNP153 33..33 33 - - - 50916 RMVar_ID_50916 Human_SNP_ID_543282150 A-to-I Human chr13 - 102247369 102247360 102247369 TGTTTGATTTTTTTTTCTTGTAAATTTCTTTAAGTTCTTTATAGATGCTGGATATTAGACCTCAG TGTTTGATTTTTTTTTCTTGTAAATTTCTTTA_________TAGATGCTGGATATTAGACCTCAG ATAAAGAACT A FGF14 Ensembl:ENSG00000102466 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1404493892 Functional Loss DEL dbSNP153 33..41 33 - - - 50917 RMVar_ID_50917 Human_SNP_ID_543282153 A-to-I Human chr13 - 102247369 102247369 102247369 TGTTTGATTTTTTTTTCTTGTAAATTTCTTTAAGTTCTTTATAGATGCTGGATATTAGACCTCAG TGTTTGATTTTTTTTTCTTGTAAATTTCTTTAGGTTCTTTATAGATGCTGGATATTAGACCTCAG T C FGF14 Ensembl:ENSG00000102466 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1480444629 Functional Loss SNV dbSNP153 33..33 33 - - - 50918 RMVar_ID_50918 Human_SNP_ID_543282197 A-to-I Human chr13 - 102247519 102247519 102247519 TGTGAAATGGTATCTCATTGTGGTTTTGATTTACATTTTTCTAATGATCAGTGATATTGAGGGTT TGTGAAATGGTATCTCATTGTGGTTTTGATTTCCATTTTTCTAATGATCAGTGATATTGAGGGTT T G FGF14 Ensembl:ENSG00000102466 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs564498860 Functional Loss SNV dbSNP153 33..33 33 - - - 50919 RMVar_ID_50919 Human_SNP_ID_543283537 A-to-I Human chr13 - 102253037 102253037 102253037 ATTATAGACTGGATAAAGAATATGTGGCACATATACACCATGGAATACTATGCAGCCATAAAAAA ATTATAGACTGGATAAAGAATATGTGGCACATTTACACCATGGAATACTATGCAGCCATAAAAAA T A FGF14 Ensembl:ENSG00000102466 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs765558190 Functional Loss SNV dbSNP153 33..33 33 - - - 50920 RMVar_ID_50920 Human_SNP_ID_543284313 A-to-I Human chr13 - 102256373 102256373 102256373 CCACCTCACCGTGCTGAGTACCTGGGACTACAATGTGTCCCACCATGCTTGGCTAATTTTTTTTT CCACCTCACCGTGCTGAGTACCTGGGACTACAGTGTGTCCCACCATGCTTGGCTAATTTTTTTTT T C FGF14 Ensembl:ENSG00000102466 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs543451184 Functional Loss SNV dbSNP153 33..33 33 - - - 50921 RMVar_ID_50921 Human_SNP_ID_543284617 A-to-I Human chr13 - 102257490 102257490 102257490 AAAATTAGCTGGGCGTTGTGATGTATGCCTATAGTCCCAACTACTCAGGCTCCTGGGGCAGAAGA AAAATTAGCTGGGCGTTGTGATGTATGCCTATGGTCCCAACTACTCAGGCTCCTGGGGCAGAAGA T C FGF14 Ensembl:ENSG00000102466 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs531722405 Functional Loss SNV dbSNP153 33..33 33 - - - 50922 RMVar_ID_50922 Human_SNP_ID_543284618 A-to-I Human chr13 - 102257492 102257492 102257492 CAAAAATTAGCTGGGCGTTGTGATGTATGCCTATAGTCCCAACTACTCAGGCTCCTGGGGCAGAA CAAAAATTAGCTGGGCGTTGTGATGTATGCCTGTAGTCCCAACTACTCAGGCTCCTGGGGCAGAA T C FGF14 Ensembl:ENSG00000102466 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1179248226 Functional Loss SNV dbSNP153 33..33 33 - - - 50923 RMVar_ID_50923 Human_SNP_ID_543287415 A-to-I Human chr13 - 102269761 102269761 102269761 GGCTCAAGCAATCCCCCTGCCTCATTCTCCCGAGTAGCGGGGATTACAGGTATGTGCCACCACAT GGCTCAAGCAATCCCCCTGCCTCATTCTCCCGCGTAGCGGGGATTACAGGTATGTGCCACCACAT T G FGF14 Ensembl:ENSG00000102466 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1455090384 Functional Loss SNV dbSNP153 33..33 33 - - - 50924 RMVar_ID_50924 Human_SNP_ID_543287423 A-to-I Human chr13 - 102269783 102269783 102269783 CCAGGCTGGCCTTGAACTCCTAGGCTCAAGCAATCCCCCTGCCTCATTCTCCCGAGTAGCGGGGA CCAGGCTGGCCTTGAACTCCTAGGCTCAAGCAGTCCCCCTGCCTCATTCTCCCGAGTAGCGGGGA T C FGF14 Ensembl:ENSG00000102466 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs866376246 Functional Loss SNV dbSNP153 33..33 33 - - - 50925 RMVar_ID_50925 Human_SNP_ID_543306362 A-to-I Human chr13 - 102350360 102350360 102350360 TTTTTTTTTTTTTTTTAATTAAAGAGGGTTTCACTCTGTCACCTAGGCTGGAGTGCAGTGCGATG TTTTTTTTTTTTTTTTAATTAAAGAGGGTTTCGCTCTGTCACCTAGGCTGGAGTGCAGTGCGATG T C FGF14-IT1,FGF14 Ensembl:ENSG00000243319,Ensembl:ENSG00000102466 lincRNA,Protein coding intron,intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1006506138 Functional Loss SNV dbSNP153 33..33 33 - - - 50926 RMVar_ID_50926 Human_SNP_ID_543307363 A-to-I Human chr13 - 102354143 102354143 102354143 GAACTCCTTTAAGATAAAGATCTTGAGTCCCAAAAGGAATTTCCTAGTGGGCAAATTGTGAGGGA GAACTCCTTTAAGATAAAGATCTTGAGTCCCAGAAGGAATTTCCTAGTGGGCAAATTGTGAGGGA T C FGF14-IT1,FGF14 Ensembl:ENSG00000243319,Ensembl:ENSG00000102466 lincRNA,Protein coding intron,intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs891546274 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_1479516,Human_Splice_Rec_1479517 50927 RMVar_ID_50927 Human_SNP_ID_543307477 A-to-I Human chr13 - 102354624 102354624 102354624 AAGCTACATACCTTCCTCACAATTTGCCTACAAGGAAATTCTTTGTGGGCCTCAAGATGATGACA AAGCTACATACCTTCCTCACAATTTGCCTACAGGGAAATTCTTTGTGGGCCTCAAGATGATGACA T C FGF14-IT1,FGF14 Ensembl:ENSG00000243319,Ensembl:ENSG00000102466 lincRNA,Protein coding intron,intron GSE107867 ASD brains,cerebellum;ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1229775787 Functional Loss SNV dbSNP153 33..33 33 - - - 50928 RMVar_ID_50928 Human_SNP_ID_543311030 A-to-I Human chr13 - 102370192 102370192 102370192 GGCCAGGAGTTCAAGAGCAGCCTTAGCAACATAGTGAAACCCTGTCTCTACAAAAAATTTAAAAA GGCCAGGAGTTCAAGAGCAGCCTTAGCAACATTGTGAAACCCTGTCTCTACAAAAAATTTAAAAA T A FGF14-IT1,FGF14 Ensembl:ENSG00000243319,Ensembl:ENSG00000102466 lincRNA,Protein coding intron,intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1028273262 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3440352 50929 RMVar_ID_50929 Human_SNP_ID_543380747 A-to-I Human chr13 + 102653467 102653467 102653467 CAGGCTAGAGTACAGTGGCATGATCGTAGCTCACTGTTGCCTCCAGCTCCTGGGCTCAAGTGATC CAGGCTAGAGTACAGTGGCATGATCGTAGCTCTCTGTTGCCTCCAGCTCCTGGGCTCAAGTGATC A T TPP2 Ensembl:ENSG00000134900 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1236463576 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54476,RMVar_hsa_circ_72039,RMVar_hsa_circ_32266,RMVar_hsa_circ_55799,RMVar_hsa_circ_164545,RMVar_hsa_circ_328123,RMVar_hsa_circ_164556,RMVar_hsa_circ_120165,RMVar_hsa_circ_164557,RMVar_hsa_circ_164562,RMVar_hsa_circ_28062,RMVar_hsa_circ_68063,RMVar_hsa_circ_31247,RMVar_hsa_circ_164567,RMVar_hsa_circ_164569,RMVar_hsa_circ_93497,RMVar_hsa_circ_103105,RMVar_hsa_circ_164570,RMVar_hsa_circ_87571,RMVar_hsa_circ_164573,RMVar_hsa_circ_70860,RMVar_hsa_circ_164574,RMVar_hsa_circ_164576,RMVar_hsa_circ_81739,RMVar_hsa_circ_279148,RMVar_hsa_circ_164577,RMVar_hsa_circ_356980 50930 RMVar_ID_50930 Human_SNP_ID_543380751 A-to-I Human chr13 + 102653492 102653492 102653492 GTAGCTCACTGTTGCCTCCAGCTCCTGGGCTCAAGTGATCCTCCCACCTCAGCCTCCCTAGAGTG GTAGCTCACTGTTGCCTCCAGCTCCTGGGCTCGAGTGATCCTCCCACCTCAGCCTCCCTAGAGTG A G TPP2 Ensembl:ENSG00000134900 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1443928964 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54476,RMVar_hsa_circ_72039,RMVar_hsa_circ_32266,RMVar_hsa_circ_55799,RMVar_hsa_circ_164545,RMVar_hsa_circ_328123,RMVar_hsa_circ_164556,RMVar_hsa_circ_120165,RMVar_hsa_circ_164557,RMVar_hsa_circ_164562,RMVar_hsa_circ_28062,RMVar_hsa_circ_68063,RMVar_hsa_circ_31247,RMVar_hsa_circ_164567,RMVar_hsa_circ_164569,RMVar_hsa_circ_93497,RMVar_hsa_circ_103105,RMVar_hsa_circ_164570,RMVar_hsa_circ_87571,RMVar_hsa_circ_164573,RMVar_hsa_circ_70860,RMVar_hsa_circ_164574,RMVar_hsa_circ_164576,RMVar_hsa_circ_81739,RMVar_hsa_circ_279148,RMVar_hsa_circ_164577,RMVar_hsa_circ_356980 50931 RMVar_ID_50931 Human_SNP_ID_543380753 A-to-I Human chr13 + 102653497 102653497 102653497 TCACTGTTGCCTCCAGCTCCTGGGCTCAAGTGATCCTCCCACCTCAGCCTCCCTAGAGTGGCTGG TCACTGTTGCCTCCAGCTCCTGGGCTCAAGTGGTCCTCCCACCTCAGCCTCCCTAGAGTGGCTGG A G TPP2 Ensembl:ENSG00000134900 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1009337183 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25030342 RMVar_hsa_circ_54476,RMVar_hsa_circ_72039,RMVar_hsa_circ_32266,RMVar_hsa_circ_55799,RMVar_hsa_circ_164545,RMVar_hsa_circ_328123,RMVar_hsa_circ_164556,RMVar_hsa_circ_120165,RMVar_hsa_circ_164557,RMVar_hsa_circ_164562,RMVar_hsa_circ_28062,RMVar_hsa_circ_68063,RMVar_hsa_circ_31247,RMVar_hsa_circ_164567,RMVar_hsa_circ_164569,RMVar_hsa_circ_93497,RMVar_hsa_circ_103105,RMVar_hsa_circ_164570,RMVar_hsa_circ_87571,RMVar_hsa_circ_164573,RMVar_hsa_circ_70860,RMVar_hsa_circ_164574,RMVar_hsa_circ_164576,RMVar_hsa_circ_81739,RMVar_hsa_circ_279148,RMVar_hsa_circ_164577,RMVar_hsa_circ_356980 50932 RMVar_ID_50932 Human_SNP_ID_543421245 A-to-I Human chr13 + 102802845 102802845 102802845 ATAGCTCACTGCAGCCTCAAACTCCTGGCCTCAAGTGATTCTTTTGCCTCAGCCTCCCAAAGCAT ATAGCTCACTGCAGCCTCAAACTCCTGGCCTCCAGTGATTCTTTTGCCTCAGCCTCCCAAAGCAT A C BIVM-ERCC5,BIVM Ensembl:ENSG00000270181,Ensembl:ENSG00000134897 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1168838450 Functional Loss SNV dbSNP153 33..33 33 - - - 50933 RMVar_ID_50933 Human_SNP_ID_543421635 A-to-I Human chr13 + 102804497 102804497 102804497 CATGCCCAGCTAATTTTTTTGTGTTTTTTAGTAGAGACAGGGTTTCACCCTGTGTGCCAGGCTGG CATGCCCAGCTAATTTTTTTGTGTTTTTTAGTGGAGACAGGGTTTCACCCTGTGTGCCAGGCTGG A G BIVM-ERCC5,BIVM Ensembl:ENSG00000270181,Ensembl:ENSG00000134897 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs768340953 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9718166,Human_RBP_ID_12094906,Human_RBP_ID_24468804 50934 RMVar_ID_50934 Human_SNP_ID_543421654 A-to-I Human chr13 + 102804554 102804554 102804554 CAGGCTGGTCTCGAACTCTGACCTCATGATCCACCCGCCTCGGCCTCCTACAGTGCTGGGATTAC CAGGCTGGTCTCGAACTCTGACCTCATGATCCCCCCGCCTCGGCCTCCTACAGTGCTGGGATTAC A C BIVM-ERCC5,BIVM Ensembl:ENSG00000270181,Ensembl:ENSG00000134897 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs994530745 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12094911 50935 RMVar_ID_50935 Human_SNP_ID_543428093 A-to-I Human chr13 + 102833128 102833128 102833128 AAAAAATACAAAAGTTAGCTGAGTGTGTTGGTATGCACCTGTAGTCCCAGCTACTTGGGAGGCTG AAAAAATACAAAAGTTAGCTGAGTGTGTTGGTGTGCACCTGTAGTCCCAGCTACTTGGGAGGCTG A G ERCC5,BIVM-ERCC5,BIVM Ensembl:ENSG00000134899,Ensembl:ENSG00000270181,Ensembl:ENSG00000134897 Protein coding,Protein coding,Protein coding intron,intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs531138481 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_164592,RMVar_hsa_circ_324448,RMVar_hsa_circ_311604,RMVar_hsa_circ_164590,RMVar_hsa_circ_164591,RMVar_hsa_circ_97419,RMVar_hsa_circ_303981,RMVar_hsa_circ_164593,RMVar_hsa_circ_20045,RMVar_hsa_circ_33399,RMVar_hsa_circ_164597,RMVar_hsa_circ_334133,RMVar_hsa_circ_311023,RMVar_hsa_circ_91981,RMVar_hsa_circ_164601,RMVar_hsa_circ_318749,RMVar_hsa_circ_164603,RMVar_hsa_circ_164604,RMVar_hsa_circ_317747 50936 RMVar_ID_50936 Human_SNP_ID_543428692 A-to-I Human chr13 + 102835577 102835577 102835577 TTTTTTTAAGACAGAGTCTCTTTCTGTCACTTAGGTGGGAGTGCAGTGGTGTGATGTCAGCTCAC TTTTTTTAAGACAGAGTCTCTTTCTGTCACTTGGGTGGGAGTGCAGTGGTGTGATGTCAGCTCAC A G ERCC5,BIVM-ERCC5,BIVM Ensembl:ENSG00000134899,Ensembl:ENSG00000270181,Ensembl:ENSG00000134897 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs368313329 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2370746,Human_RBP_ID_17833157 RMVar_hsa_circ_164592,RMVar_hsa_circ_324448,RMVar_hsa_circ_164591,RMVar_hsa_circ_97419,RMVar_hsa_circ_91981,RMVar_hsa_circ_164604,RMVar_hsa_circ_86825,RMVar_hsa_circ_164606 50937 RMVar_ID_50937 Human_SNP_ID_543429033 A-to-I Human chr13 + 102837131 102837131 102837131 GAAACCCCATCTCTACTAAAACGACAAAAATTAGCCAGGCATGGTGGCATGTGCGTGTAGTTTCA GAAACCCCATCTCTACTAAAACGACAAAAATTGGCCAGGCATGGTGGCATGTGCGTGTAGTTTCA A G ERCC5,BIVM-ERCC5,BIVM Ensembl:ENSG00000134899,Ensembl:ENSG00000270181,Ensembl:ENSG00000134897 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1027351705 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_164592,RMVar_hsa_circ_324448,RMVar_hsa_circ_164591,RMVar_hsa_circ_97419,RMVar_hsa_circ_91981,RMVar_hsa_circ_164604,RMVar_hsa_circ_86825,RMVar_hsa_circ_164606 50938 RMVar_ID_50938 Human_SNP_ID_372889375 A-to-I Human chr8 - 91069333 91069333 91069333 TGGAAAAGGCTCATAGGATACCTTTAAAGTTTAATGAAAAGAAAGCAGCATCTAGACATATCCGG TGGAAAAGGCTCATAGGATACCTTTAAAGTTTGATGAAAAGAAAGCAGCATCTAGACATATCCGG T C OTUD6B-AS1 Ensembl:ENSG00000253738 lincRNA intron GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1358426471 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3888519 50939 RMVar_ID_50939 Human_SNP_ID_372896920 A-to-I Human chr8 + 91100936 91100936 91100936 TTTGTGTTCCCTCCAAAATCTCATGTTCAATTATAATCCCCAGTGTTGGAGACTGGGCCTGGTGG TTTGTGTTCCCTCCAAAATCTCATGTTCAATTTTAATCCCCAGTGTTGGAGACTGGGCCTGGTGG A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs557296447 Functional Loss SNV dbSNP153 33..33 33 - - - 50940 RMVar_ID_50940 Human_SNP_ID_373105589 A-to-I Human chr8 - 91959656 91959656 91959656 AAACGCGCAGATGTGCAGCAGATTGGAAGGAGACACAGATGTTCGGTTTTTTTCCTGTTTCTGAA AAACGCGCAGATGTGCAGCAGATTGGAAGGAGTCACAGATGTTCGGTTTTTTTCCTGTTTCTGAA T A RUNX1T1 Ensembl:ENSG00000079102 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs757871809 Functional Loss SNV dbSNP153 33..33 33 - - - 50941 RMVar_ID_50941 Human_SNP_ID_373348000 A-to-I Human chr8 - 92950275 92950275 92950275 CTGATAAAAATCCCTGGGGGAGGGGAAAAGGAACCATTTTGAAATACACCACAGCACTCTGTTCT CTGATAAAAATCCCTGGGGGAGGGGAAAAGGAGCCATTTTGAAATACACCACAGCACTCTGTTCT T C TRIQK Ensembl:ENSG00000205133 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1409699840 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_298816,RMVar_hsa_circ_272267,RMVar_hsa_circ_253057 50942 RMVar_ID_50942 Human_SNP_ID_373526911 A-to-I Human chr8 - 93716172 93716172 93716172 GGGCATGGTGGTGCACGCCTGTAATGCCAGCTACTTGGGTGGCTGAGGCAGGAGAATCACTTGAA GGGCATGGTGGTGCACGCCTGTAATGCCAGCTGCTTGGGTGGCTGAGGCAGGAGAATCACTTGAA T C - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1210370773 Functional Loss SNV dbSNP153 33..33 33 - - - 50943 RMVar_ID_50943 Human_SNP_ID_373527541 A-to-I Human chr8 - 93718996 93718996 93718996 AGCTGGGCATGGTGGCGGGCACCTGTAATCCAAGCTAGTTAGGAGGCTGAGGCAGAAGAATTGCT AGCTGGGCATGGTGGCGGGCACCTGTAATCCATGCTAGTTAGGAGGCTGAGGCAGAAGAATTGCT T A - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1037408692 Functional Loss SNV dbSNP153 33..33 33 - - - 50944 RMVar_ID_50944 Human_SNP_ID_373527566 A-to-I Human chr8 - 93719101 93719099 93719101 CCAGCACTTTGGGAGGCCGAGGTGGGCGTATCACTTGAGATCAGGAGTTCAAGACCAGCCTGGCT CCAGCACTTTGGGAGGCCGAGGTGGGCGTATC__TTGAGATCAGGAGTTCAAGACCAGCCTGGCT AGT A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1210004605 Functional Loss DEL dbSNP153 33..34 33 - - - 50945 RMVar_ID_50945 Human_SNP_ID_373527569 A-to-I Human chr8 - 93719101 93719101 93719101 CCAGCACTTTGGGAGGCCGAGGTGGGCGTATCACTTGAGATCAGGAGTTCAAGACCAGCCTGGCT CCAGCACTTTGGGAGGCCGAGGTGGGCGTATCTCTTGAGATCAGGAGTTCAAGACCAGCCTGGCT T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910984676 Functional Loss SNV dbSNP153 33..33 33 - - - 50946 RMVar_ID_50946 Human_SNP_ID_373527570 A-to-I Human chr8 - 93719101 93719101 93719101 CCAGCACTTTGGGAGGCCGAGGTGGGCGTATCACTTGAGATCAGGAGTTCAAGACCAGCCTGGCT CCAGCACTTTGGGAGGCCGAGGTGGGCGTATCGCTTGAGATCAGGAGTTCAAGACCAGCCTGGCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs910984676 Functional Loss SNV dbSNP153 33..33 33 - - - 50947 RMVar_ID_50947 Human_SNP_ID_373527795 A-to-I Human chr8 - 93720014 93720014 93720014 GCACCACTGCACTCCAGACTGGGTGACAGAGCAAGACTCTGTCTTGGAAGGCGGGGGAAGATACA GCACCACTGCACTCCAGACTGGGTGACAGAGCGAGACTCTGTCTTGGAAGGCGGGGGAAGATACA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1221045155 Functional Loss SNV dbSNP153 33..33 33 - - - 50948 RMVar_ID_50948 Human_SNP_ID_373528001 A-to-I Human chr8 - 93720793 93720793 93720793 GATCTTGGCTCACTGCAAACTCTGACGCCCGGATTCAAGCGATTCTTCTGCCTCAGCCTCCCGAG GATCTTGGCTCACTGCAAACTCTGACGCCCGGCTTCAAGCGATTCTTCTGCCTCAGCCTCCCGAG T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1011903559 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16489571,Human_RBP_ID_26185134 50949 RMVar_ID_50949 Human_SNP_ID_373528577 A-to-I Human chr8 - 93723121 93723121 93723121 GAGGTGGCGGGTGCCTGTAGTCCCAGCTAGTCAGGAGGCTGAAGCAGGAGAATGGTGTGAATCCG GAGGTGGCGGGTGCCTGTAGTCCCAGCTAGTCGGGAGGCTGAAGCAGGAGAATGGTGTGAATCCG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs542461029 Functional Loss SNV dbSNP153 33..33 33 - - - 50950 RMVar_ID_50950 Human_SNP_ID_373530305 A-to-I Human chr8 - 93730019 93730014 93730019 GATGCTCAAAGAAAATGCTCATTGCAGCATTTAAGATTTCAGATTTTTGGGTTAGGAATGTTGAA GATGCTCAAAGAAAATGCTCATTGCAGCATTT_____TTCAGATTTTTGGGTTAGGAATGTTGAA AATCTT A RBM12B Ensembl:ENSG00000183808 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1366987345 Functional Loss DEL dbSNP153 33..37 33 - - - Human_RBP_ID_27780328 50951 RMVar_ID_50951 Human_SNP_ID_373550799 A-to-I Human chr8 + 93811894 93811894 93811894 TAATGGGGCCAGGTGCGGTGGCTCATGCCTGTAATCCTAGCACTTTGGGAGGCCGAGGCAGGTGG TAATGGGGCCAGGTGCGGTGGCTCATGCCTGTGATCCTAGCACTTTGGGAGGCCGAGGCAGGTGG A G TMEM67 Ensembl:ENSG00000164953 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs13271258 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_253066,RMVar_hsa_circ_96388,RMVar_hsa_circ_253071,RMVar_hsa_circ_282018,RMVar_hsa_circ_266757,RMVar_hsa_circ_253073,RMVar_hsa_circ_314672,RMVar_hsa_circ_253075,RMVar_hsa_circ_35541,RMVar_hsa_circ_253084,RMVar_hsa_circ_337207,RMVar_hsa_circ_253078,RMVar_hsa_circ_253080,RMVar_hsa_circ_288457,RMVar_hsa_circ_102880,RMVar_hsa_circ_253085,RMVar_hsa_circ_253082,RMVar_hsa_circ_253083,RMVar_hsa_circ_253081,RMVar_hsa_circ_59525,RMVar_hsa_circ_41168,RMVar_hsa_circ_253091 50952 RMVar_ID_50952 Human_SNP_ID_373552460 A-to-I Human chr8 + 93819019 93819019 93819019 TAGAGACAAGGGTTCACCATGTTGCCCAGGCTAGTCTTGAACTCCTGATCGAGAGATTCACCCAC TAGAGACAAGGGTTCACCATGTTGCCCAGGCTGGTCTTGAACTCCTGATCGAGAGATTCACCCAC A G TMEM67 Ensembl:ENSG00000164953 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1349026055 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_993518 RMVar_hsa_circ_253080,RMVar_hsa_circ_253082,RMVar_hsa_circ_253083,RMVar_hsa_circ_253081 50953 RMVar_ID_50953 Human_SNP_ID_373656547 A-to-I Human chr8 - 94249271 94249271 94249271 AAGTTTTTACCTATATGTCTTATAATAAAAGAAATAAAATATTTGAAAAAAGGCATTCTTGATTG AAGTTTTTACCTATATGTCTTATAATAAAAGATATAAAATATTTGAAAAAAGGCATTCTTGATTG T A GEM Ensembl:ENSG00000164949 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1356465763 Functional Loss SNV dbSNP153 33..33 33 - - - 50954 RMVar_ID_50954 Human_SNP_ID_373689868 A-to-I Human chr8 - 94402533 94402533 94402533 ATTGGAAAAATAGGCTGGGCATGGTGGCTTACACCTGTAATCCCAGCATTTTCGGAGGCCAAGGC ATTGGAAAAATAGGCTGGGCATGGTGGCTTACTCCTGTAATCCCAGCATTTTCGGAGGCCAAGGC T A RAD54B,FSBP Ensembl:ENSG00000197275,Ensembl:ENSG00000265817 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs543732592 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92386,RMVar_hsa_circ_253095,RMVar_hsa_circ_253093,RMVar_hsa_circ_288015,RMVar_hsa_circ_313897,RMVar_hsa_circ_368728,RMVar_hsa_circ_253096,RMVar_hsa_circ_54931,RMVar_hsa_circ_299535,RMVar_hsa_circ_253094,RMVar_hsa_circ_286473,RMVar_hsa_circ_253098,RMVar_hsa_circ_253097,RMVar_hsa_circ_374970,RMVar_hsa_circ_292568,RMVar_hsa_circ_253099,RMVar_hsa_circ_253100,RMVar_hsa_circ_344960,RMVar_hsa_circ_366354,RMVar_hsa_circ_46226,RMVar_hsa_circ_253101,RMVar_hsa_circ_321392,RMVar_hsa_circ_253102,RMVar_hsa_circ_253103,RMVar_hsa_circ_75267 50955 RMVar_ID_50955 Human_SNP_ID_373691994 A-to-I Human chr8 - 94412132 94412128 94412132 CATTATGCTCAGTGAAATAAGCTGGACACAGAAAGACAATTATTGTGTGATCTCACTTATGTGTG CATTATGCTCAGTGAAATAAGCTGGACACAGA____CAATTATTGTGTGATCTCACTTATGTGTG GTCTT G RAD54B,FSBP Ensembl:ENSG00000197275,Ensembl:ENSG00000265817 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1182391287 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_92386,RMVar_hsa_circ_54931,RMVar_hsa_circ_253094,RMVar_hsa_circ_292568,RMVar_hsa_circ_253100,RMVar_hsa_circ_253103,RMVar_hsa_circ_253104 50956 RMVar_ID_50956 Human_SNP_ID_373695485 A-to-I Human chr8 - 94426015 94426015 94426015 CTGGGAGGCAGAGGTTGCAGTGAGCCCTGATGACGCCACTGTACTCCAGCTTGGGCAACAGAGCA CTGGGAGGCAGAGGTTGCAGTGAGCCCTGATGGCGCCACTGTACTCCAGCTTGGGCAACAGAGCA T C RAD54B,FSBP Ensembl:ENSG00000197275,Ensembl:ENSG00000265817 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1279063913 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16493004 RMVar_hsa_circ_92386,RMVar_hsa_circ_54931,RMVar_hsa_circ_253094,RMVar_hsa_circ_292568,RMVar_hsa_circ_253103 50957 RMVar_ID_50957 Human_SNP_ID_373700725 A-to-I Human chr8 - 94449424 94449424 94449424 TTGTATTTTTTTAGTGGAAACAGGGTTTCACCATGTTGGCCAGCTGGTCTTGAACTCCCGACCTC TTGTATTTTTTTAGTGGAAACAGGGTTTCACCGTGTTGGCCAGCTGGTCTTGAACTCCCGACCTC T C RAD54B Ensembl:ENSG00000197275 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs904898631 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16493737 RMVar_hsa_circ_54931,RMVar_hsa_circ_253094,RMVar_hsa_circ_292568,RMVar_hsa_circ_65104 50958 RMVar_ID_50958 Human_SNP_ID_373710786 A-to-I Human chr8 - 94492798 94492798 94492798 TTATGACTGCAGGTAAAGGTTGACTTAATTGAACTCTCTGAAAAATGCTGTAGTGACTTTGATTT TTATGACTGCAGGTAAAGGTTGACTTAATTGACCTCTCTGAAAAATGCTGTAGTGACTTTGATTT T G VIRMA Ensembl:ENSG00000164944 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs772231079 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_705972,Human_RBP_ID_8692240,Human_RBP_ID_8922478,Human_RBP_ID_24272328 Human_Splice_Rec_993890,Human_Splice_Rec_993908,Human_Splice_Rec_993938,Human_Splice_Rec_993952 Human_miRNA_ID_652078 RMVar_hsa_circ_102204,RMVar_hsa_circ_125301,RMVar_hsa_circ_69380,RMVar_hsa_circ_289600,RMVar_hsa_circ_253108,RMVar_hsa_circ_322018,RMVar_hsa_circ_51210,RMVar_hsa_circ_81033,RMVar_hsa_circ_253111,RMVar_hsa_circ_37180,RMVar_hsa_circ_253110 50959 RMVar_ID_50959 Human_SNP_ID_373712532 A-to-I Human chr8 - 94499842 94499842 94499842 CCGGGTTACCCTATGTTGGCCAGGCTGCTCTTAAACTCCTGACCTCAAGTGATCCACCACCTTCG CCGGGTTACCCTATGTTGGCCAGGCTGCTCTTGAACTCCTGACCTCAAGTGATCCACCACCTTCG T C VIRMA Ensembl:ENSG00000164944 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1013666268 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102204,RMVar_hsa_circ_125301,RMVar_hsa_circ_253108,RMVar_hsa_circ_51210,RMVar_hsa_circ_81033,RMVar_hsa_circ_253111,RMVar_hsa_circ_253110,RMVar_hsa_circ_253114,RMVar_hsa_circ_51377,RMVar_hsa_circ_295479,RMVar_hsa_circ_305735,RMVar_hsa_circ_357472,RMVar_hsa_circ_105883,RMVar_hsa_circ_253115 50960 RMVar_ID_50960 Human_SNP_ID_373714747 A-to-I Human chr8 - 94508238 94508238 94508238 CTACTACAAAAAAACTAGCTGGGCGTGGTGGCATGCATCTGTAGTCCCAGCTACTTGGGAGGCAG CTACTACAAAAAAACTAGCTGGGCGTGGTGGCGTGCATCTGTAGTCCCAGCTACTTGGGAGGCAG T C VIRMA Ensembl:ENSG00000164944 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs927813917 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102204,RMVar_hsa_circ_125301,RMVar_hsa_circ_253108,RMVar_hsa_circ_51210,RMVar_hsa_circ_81033,RMVar_hsa_circ_253111,RMVar_hsa_circ_253110,RMVar_hsa_circ_253114,RMVar_hsa_circ_51377,RMVar_hsa_circ_295479,RMVar_hsa_circ_305735,RMVar_hsa_circ_357472,RMVar_hsa_circ_105883,RMVar_hsa_circ_253115,RMVar_hsa_circ_253118,RMVar_hsa_circ_283072,RMVar_hsa_circ_299311,RMVar_hsa_circ_350816,RMVar_hsa_circ_271989,RMVar_hsa_circ_253116,RMVar_hsa_circ_253117 50961 RMVar_ID_50961 Human_SNP_ID_373716705 A-to-I Human chr8 - 94515651 94515651 94515651 CTAAATTGTTTAAGCTGGGCGCGGTGGCTCACACTTGTAATTCCAGCACTTTGGGAGGCTGAGGT CTAAATTGTTTAAGCTGGGCGCGGTGGCTCACTCTTGTAATTCCAGCACTTTGGGAGGCTGAGGT T A VIRMA Ensembl:ENSG00000164944 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1318882278 Functional Loss SNV dbSNP153 33..33 33 - - - 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_53665,RMVar_hsa_circ_84120,RMVar_hsa_circ_253123,RMVar_hsa_circ_253124,RMVar_hsa_circ_365178 50962 RMVar_ID_50962 Human_SNP_ID_373768818 A-to-I Human chr8 - 94718708 94718708 94718708 GATGGGATTTCACCATGTTGGTTGGCCAGGCTAGTCTCCAACTCCTGGCCTCAAGTGATCCGCCC GATGGGATTTCACCATGTTGGTTGGCCAGGCTGGTCTCCAACTCCTGGCCTCAAGTGATCCGCCC T C RF00017-1304,RF00017-4495,lnc-CCNE2-2 RNACentral:URS0000990DE9,RNACentral:URS0000923EDC,RNACentral:URS0000D59115 SRP RNA,SRP RNA,lincRNA intron,intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs865989113 Functional Loss SNV dbSNP153 33..33 33 - - - 50963 RMVar_ID_50963 Human_SNP_ID_373774841 A-to-I Human chr8 + 94742505 94742505 94742505 ACCTCTGGCTCATGGATGCAAGTGATTCTCCCACCTCAGCCTCCCCAGTAGCTGGGACCACAGGC ACCTCTGGCTCATGGATGCAAGTGATTCTCCCCCCTCAGCCTCCCCAGTAGCTGGGACCACAGGC A C DPY19L4 Ensembl:ENSG00000156162 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1044867126 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61206,RMVar_hsa_circ_91878,RMVar_hsa_circ_101288,RMVar_hsa_circ_70419,RMVar_hsa_circ_253147,RMVar_hsa_circ_50616,RMVar_hsa_circ_253148,RMVar_hsa_circ_306558,RMVar_hsa_circ_340330,RMVar_hsa_circ_370143,RMVar_hsa_circ_72374,RMVar_hsa_circ_20647,RMVar_hsa_circ_30857,RMVar_hsa_circ_253150,RMVar_hsa_circ_341217 50964 RMVar_ID_50964 Human_SNP_ID_373780315 A-to-I Human chr8 + 94764910 94764910 94764910 GCCACCATGCCCAGCTAATTTTTTTTGTTTTTAATAGAGATGGGTTTCACCATGTTGGCCAGGCT GCCACCATGCCCAGCTAATTTTTTTTGTTTTTTATAGAGATGGGTTTCACCATGTTGGCCAGGCT A T DPY19L4 Ensembl:ENSG00000156162 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1183420963 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91878,RMVar_hsa_circ_101288,RMVar_hsa_circ_253147,RMVar_hsa_circ_50616,RMVar_hsa_circ_253148,RMVar_hsa_circ_340330,RMVar_hsa_circ_370143,RMVar_hsa_circ_72374,RMVar_hsa_circ_20647,RMVar_hsa_circ_30857,RMVar_hsa_circ_253150,RMVar_hsa_circ_341217,RMVar_hsa_circ_253157,RMVar_hsa_circ_350453,RMVar_hsa_circ_361565,RMVar_hsa_circ_375229,RMVar_hsa_circ_356968,RMVar_hsa_circ_319350,RMVar_hsa_circ_321074,RMVar_hsa_circ_253156,RMVar_hsa_circ_46338,RMVar_hsa_circ_334486,RMVar_hsa_circ_359593 50965 RMVar_ID_50965 Human_SNP_ID_373780320 A-to-I Human chr8 + 94764929 94764929 94764929 TTTTTTTGTTTTTAATAGAGATGGGTTTCACCATGTTGGCCAGGCTTGTCTCGAACCCCTGACCT TTTTTTTGTTTTTAATAGAGATGGGTTTCACCCTGTTGGCCAGGCTTGTCTCGAACCCCTGACCT A C DPY19L4 Ensembl:ENSG00000156162 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs890222311 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91878,RMVar_hsa_circ_101288,RMVar_hsa_circ_253147,RMVar_hsa_circ_50616,RMVar_hsa_circ_253148,RMVar_hsa_circ_340330,RMVar_hsa_circ_370143,RMVar_hsa_circ_72374,RMVar_hsa_circ_20647,RMVar_hsa_circ_30857,RMVar_hsa_circ_253150,RMVar_hsa_circ_341217,RMVar_hsa_circ_253157,RMVar_hsa_circ_350453,RMVar_hsa_circ_361565,RMVar_hsa_circ_375229,RMVar_hsa_circ_356968,RMVar_hsa_circ_319350,RMVar_hsa_circ_321074,RMVar_hsa_circ_253156,RMVar_hsa_circ_46338,RMVar_hsa_circ_334486,RMVar_hsa_circ_359593 50966 RMVar_ID_50966 Human_SNP_ID_373781938 A-to-I Human chr8 + 94771106 94771106 94771106 CTGGCTAATTTTTTTGTATTTTTAGTAGAGACAGGGTTTCACCACATTGGTCAGGCTGGTCTTGA CTGGCTAATTTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCACATTGGTCAGGCTGGTCTTGA A G DPY19L4 Ensembl:ENSG00000156162 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1468185316 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101288,RMVar_hsa_circ_797,RMVar_hsa_circ_253147,RMVar_hsa_circ_50616,RMVar_hsa_circ_370143,RMVar_hsa_circ_72374,RMVar_hsa_circ_253150,RMVar_hsa_circ_356968,RMVar_hsa_circ_319350,RMVar_hsa_circ_344312,RMVar_hsa_circ_253158,RMVar_hsa_circ_350231,RMVar_hsa_circ_68965,RMVar_hsa_circ_4793,RMVar_hsa_circ_360065,RMVar_hsa_circ_39824 50967 RMVar_ID_50967 Human_SNP_ID_373781957 A-to-I Human chr8 + 94771189 94771189 94771189 TGCCCACCTTGGCCTCCCAAAGTGTTGGGATTACAGGCGTGAGCCACCGCACCCAGCAAAGATTG TGCCCACCTTGGCCTCCCAAAGTGTTGGGATTGCAGGCGTGAGCCACCGCACCCAGCAAAGATTG A G DPY19L4 Ensembl:ENSG00000156162 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs139170908 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101288,RMVar_hsa_circ_797,RMVar_hsa_circ_253147,RMVar_hsa_circ_50616,RMVar_hsa_circ_370143,RMVar_hsa_circ_72374,RMVar_hsa_circ_253150,RMVar_hsa_circ_356968,RMVar_hsa_circ_319350,RMVar_hsa_circ_344312,RMVar_hsa_circ_253158,RMVar_hsa_circ_350231,RMVar_hsa_circ_68965,RMVar_hsa_circ_4793,RMVar_hsa_circ_360065,RMVar_hsa_circ_39824 50968 RMVar_ID_50968 Human_SNP_ID_373782538 A-to-I Human chr8 + 94773778 94773778 94773778 GAGAGACAGGCTGGGTGTGGCGGCTTACGCCTATAATCCCAGCAATTTGGGAGACGGAGGCAGAT GAGAGACAGGCTGGGTGTGGCGGCTTACGCCTGTAATCCCAGCAATTTGGGAGACGGAGGCAGAT A G DPY19L4 Ensembl:ENSG00000156162 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1013431107 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101288,RMVar_hsa_circ_797,RMVar_hsa_circ_253147,RMVar_hsa_circ_50616,RMVar_hsa_circ_370143,RMVar_hsa_circ_72374,RMVar_hsa_circ_253150,RMVar_hsa_circ_356968,RMVar_hsa_circ_319350,RMVar_hsa_circ_344312,RMVar_hsa_circ_253158,RMVar_hsa_circ_350231,RMVar_hsa_circ_68965,RMVar_hsa_circ_4793,RMVar_hsa_circ_360065,RMVar_hsa_circ_39824 50969 RMVar_ID_50969 Human_SNP_ID_373782653 A-to-I Human chr8 + 94774173 94774173 94774173 TCAAGCAGTGCTCCCACGATATCCTTCCAACTAGTTGGGACCACAGACTGGTGTCACCATGCCTG TCAAGCAGTGCTCCCACGATATCCTTCCAACTGGTTGGGACCACAGACTGGTGTCACCATGCCTG A G DPY19L4 Ensembl:ENSG00000156162 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs985337324 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101288,RMVar_hsa_circ_797,RMVar_hsa_circ_253147,RMVar_hsa_circ_50616,RMVar_hsa_circ_370143,RMVar_hsa_circ_72374,RMVar_hsa_circ_253150,RMVar_hsa_circ_356968,RMVar_hsa_circ_319350,RMVar_hsa_circ_344312,RMVar_hsa_circ_253158,RMVar_hsa_circ_350231,RMVar_hsa_circ_68965,RMVar_hsa_circ_4793,RMVar_hsa_circ_360065,RMVar_hsa_circ_39824 50970 RMVar_ID_50970 Human_SNP_ID_373783174 A-to-I Human chr8 + 94776352 94776352 94776352 ACCGCACATGGCCAGATTTTTGTATTTTTAGTAGAGACGAGGTTTCACCATGTTGGCCAGGATGG ACCGCACATGGCCAGATTTTTGTATTTTTAGTCGAGACGAGGTTTCACCATGTTGGCCAGGATGG A C DPY19L4 Ensembl:ENSG00000156162 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs951240481 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_101288,RMVar_hsa_circ_797,RMVar_hsa_circ_253147,RMVar_hsa_circ_50616,RMVar_hsa_circ_370143,RMVar_hsa_circ_72374,RMVar_hsa_circ_253150,RMVar_hsa_circ_356968,RMVar_hsa_circ_319350,RMVar_hsa_circ_344312,RMVar_hsa_circ_253158,RMVar_hsa_circ_350231,RMVar_hsa_circ_68965,RMVar_hsa_circ_4793,RMVar_hsa_circ_360065,RMVar_hsa_circ_39824 50971 RMVar_ID_50971 Human_SNP_ID_373786708 A-to-I Human chr8 + 94792241 94792241 94792241 GTGCCTTGAATTTATTATTATTATTATTTTTTATTTTTTTGAGATGGAGTTTCACTCTTGTCTCC GTGCCTTGAATTTATTATTATTATTATTTTTTTTTTTTTTGAGATGGAGTTTCACTCTTGTCTCC A T DPY19L4 Ensembl:ENSG00000156162 Protein coding 3'UTR GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1032270645 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4993821,Human_RBP_ID_7867505 50972 RMVar_ID_50972 Human_SNP_ID_373786726 A-to-I Human chr8 + 94792296 94792296 94792296 TCTTGTCTCCCAGGCTGGAGTGCAATGGCGCGATCTTGGCTCACTGCAACCTCCGCTCGCTGCAA TCTTGTCTCCCAGGCTGGAGTGCAATGGCGCGTTCTTGGCTCACTGCAACCTCCGCTCGCTGCAA A T DPY19L4 Ensembl:ENSG00000156162 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs758619164 Functional Loss SNV dbSNP153 33..33 33 - - - 50973 RMVar_ID_50973 Human_SNP_ID_373786757 A-to-I Human chr8 + 94792413 94792413 94792413 GGGATTACAGGCACCTGCCACCAAGCACGGCTAATTTTTGTATTTTTAGTAGAAACGGGGTTTCG GGGATTACAGGCACCTGCCACCAAGCACGGCTGATTTTTGTATTTTTAGTAGAAACGGGGTTTCG A G DPY19L4 Ensembl:ENSG00000156162 Protein coding 3'UTR GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-Seq:(High) rs1490794801 Functional Loss SNV dbSNP153 33..33 33 - - - 50974 RMVar_ID_50974 Human_SNP_ID_373786829 A-to-I Human chr8 + 94792709 94792709 94792709 AAACCCCGTCTCTACTGAAAATACAAAAAATTAGCCGGGCAGGGTGGCGGGCGCCTGTAGTCCCA AAACCCCGTCTCTACTGAAAATACAAAAAATTGGCCGGGCAGGGTGGCGGGCGCCTGTAGTCCCA A G DPY19L4 Ensembl:ENSG00000156162 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs1465231621 Functional Loss SNV dbSNP153 33..33 33 - - - 50975 RMVar_ID_50975 Human_SNP_ID_373786862 A-to-I Human chr8 + 94792800 94792800 94792800 TGGCGTCAAGCGGCGAGGCGGAGCTTGCGGTGAGCCGAGATCATGCCGCTGCACTCCAGCCTGGG TGGCGTCAAGCGGCGAGGCGGAGCTTGCGGTGGGCCGAGATCATGCCGCTGCACTCCAGCCTGGG A G DPY19L4 Ensembl:ENSG00000156162 Protein coding 3'UTR GSE38233;GSE99789;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29796672,32596459 RNA-Seq:(High) rs773176806 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_255388 50976 RMVar_ID_50976 Human_SNP_ID_373804841 A-to-I Human chr8 + 94862027 94862027 94862027 CACTGGCACAATCTCGGCTCATTGCAACCTCTACCTCCCAGTTTCAACCCATTCTTGTGCCTCAG CACTGGCACAATCTCGGCTCATTGCAACCTCTGCCTCCCAGTTTCAACCCATTCTTGTGCCTCAG A G INTS8 Ensembl:ENSG00000164941 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006717272 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16495762 RMVar_hsa_circ_18428,RMVar_hsa_circ_375077,RMVar_hsa_circ_4762,RMVar_hsa_circ_253161,RMVar_hsa_circ_348538,RMVar_hsa_circ_344377,RMVar_hsa_circ_303925,RMVar_hsa_circ_294848,RMVar_hsa_circ_253162,RMVar_hsa_circ_253164,RMVar_hsa_circ_253163,RMVar_hsa_circ_33694,RMVar_hsa_circ_253174,RMVar_hsa_circ_340579,RMVar_hsa_circ_29281,RMVar_hsa_circ_356970,RMVar_hsa_circ_310400,RMVar_hsa_circ_40182,RMVar_hsa_circ_43348,RMVar_hsa_circ_45196,RMVar_hsa_circ_253196,RMVar_hsa_circ_253197,RMVar_hsa_circ_337784,RMVar_hsa_circ_298527,RMVar_hsa_circ_67572,RMVar_hsa_circ_253199,RMVar_hsa_circ_39008,RMVar_hsa_circ_360896,RMVar_hsa_circ_324256,RMVar_hsa_circ_324697,RMVar_hsa_circ_298109,RMVar_hsa_circ_253204,RMVar_hsa_circ_253205,RMVar_hsa_circ_253203,RMVar_hsa_circ_25421,RMVar_hsa_circ_295106,RMVar_hsa_circ_343762,RMVar_hsa_circ_71669 50977 RMVar_ID_50977 Human_SNP_ID_373804842 A-to-I Human chr8 + 94862027 94862027 94862027 CACTGGCACAATCTCGGCTCATTGCAACCTCTACCTCCCAGTTTCAACCCATTCTTGTGCCTCAG CACTGGCACAATCTCGGCTCATTGCAACCTCTTCCTCCCAGTTTCAACCCATTCTTGTGCCTCAG A T INTS8 Ensembl:ENSG00000164941 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1006717272 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16495762 RMVar_hsa_circ_18428,RMVar_hsa_circ_375077,RMVar_hsa_circ_4762,RMVar_hsa_circ_253161,RMVar_hsa_circ_348538,RMVar_hsa_circ_344377,RMVar_hsa_circ_303925,RMVar_hsa_circ_294848,RMVar_hsa_circ_253162,RMVar_hsa_circ_253164,RMVar_hsa_circ_253163,RMVar_hsa_circ_33694,RMVar_hsa_circ_253174,RMVar_hsa_circ_340579,RMVar_hsa_circ_29281,RMVar_hsa_circ_356970,RMVar_hsa_circ_310400,RMVar_hsa_circ_40182,RMVar_hsa_circ_43348,RMVar_hsa_circ_45196,RMVar_hsa_circ_253196,RMVar_hsa_circ_253197,RMVar_hsa_circ_337784,RMVar_hsa_circ_298527,RMVar_hsa_circ_67572,RMVar_hsa_circ_253199,RMVar_hsa_circ_39008,RMVar_hsa_circ_360896,RMVar_hsa_circ_324256,RMVar_hsa_circ_324697,RMVar_hsa_circ_298109,RMVar_hsa_circ_253204,RMVar_hsa_circ_253205,RMVar_hsa_circ_253203,RMVar_hsa_circ_25421,RMVar_hsa_circ_295106,RMVar_hsa_circ_343762,RMVar_hsa_circ_71669 50978 RMVar_ID_50978 Human_SNP_ID_373806580 A-to-I Human chr8 + 94868763 94868763 94868763 TGAGGTCTCAGCTCACTGCAACCTACGCCTGCAAGGTTCAAGCGATTCTCATGCCTCAGCCTGCC TGAGGTCTCAGCTCACTGCAACCTACGCCTGCGAGGTTCAAGCGATTCTCATGCCTCAGCCTGCC A G INTS8 Ensembl:ENSG00000164941 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1193527580 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_994514,Human_Splice_Rec_994515,Human_Splice_Rec_994568,Human_Splice_Rec_994569,Human_Splice_Rec_994660,Human_Splice_Rec_994661 RMVar_hsa_circ_18428,RMVar_hsa_circ_348538,RMVar_hsa_circ_253162,RMVar_hsa_circ_33694,RMVar_hsa_circ_253174,RMVar_hsa_circ_340579,RMVar_hsa_circ_43348,RMVar_hsa_circ_337784,RMVar_hsa_circ_298527,RMVar_hsa_circ_67572,RMVar_hsa_circ_253199,RMVar_hsa_circ_39008,RMVar_hsa_circ_360896,RMVar_hsa_circ_71669,RMVar_hsa_circ_71463,RMVar_hsa_circ_57612,RMVar_hsa_circ_99978,RMVar_hsa_circ_343453,RMVar_hsa_circ_366057,RMVar_hsa_circ_253207,RMVar_hsa_circ_253208,RMVar_hsa_circ_269310,RMVar_hsa_circ_278144,RMVar_hsa_circ_253210,RMVar_hsa_circ_57723,RMVar_hsa_circ_281304,RMVar_hsa_circ_253211 50979 RMVar_ID_50979 Human_SNP_ID_373809974 A-to-I Human chr8 - 94882235 94882235 94882235 AGAATGTGTAGATTGGATGGTACCTTTTGTCAATGTAGTAAAAAGTACTAGTCCAGTGAAGCTGA AGAATGTGTAGATTGGATGGTACCTTTTGTCAGTGTAGTAAAAAGTACTAGTCCAGTGAAGCTGA T C CCNE2 Ensembl:ENSG00000175305 Protein coding CDS GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs933783876 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16496035,Human_RBP_ID_24272654 Human_Splice_Rec_994704,Human_Splice_Rec_994726,Human_Splice_Rec_994748 Human_miRNA_ID_158336 RMVar_hsa_circ_53725 50980 RMVar_ID_50980 Human_SNP_ID_373811153 A-to-I Human chr8 - 94886579 94886579 94886579 CTCCCACCTCAGCCTCTGGAATAGCTGAGACTACAGGGATCCACCACCATGCCTGGCTATTTTTT CTCCCACCTCAGCCTCTGGAATAGCTGAGACTGCAGGGATCCACCACCATGCCTGGCTATTTTTT T C CCNE2 Ensembl:ENSG00000175305 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893931978 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_253214,RMVar_hsa_circ_53725,RMVar_hsa_circ_79006 50981 RMVar_ID_50981 Human_SNP_ID_373811565 A-to-I Human chr8 - 94888681 94888681 94888681 TCTCTACTAAAAATACAAAAAATTAGCTGGGCATGGTGGCACACACCTGTAATCTCAGCTACTCA TCTCTACTAAAAATACAAAAAATTAGCTGGGCCTGGTGGCACACACCTGTAATCTCAGCTACTCA T G CCNE2 Ensembl:ENSG00000175305 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs770244391 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_253214,RMVar_hsa_circ_53725,RMVar_hsa_circ_79006,RMVar_hsa_circ_315486,RMVar_hsa_circ_253215 50982 RMVar_ID_50982 Human_SNP_ID_373811646 A-to-I Human chr8 - 94889001 94889001 94889001 TGGGATTACAGGCGCAGGCCACCACACCTGCTATATTTTGTATTTTTAATAGAGATGCGGTTTCA TGGGATTACAGGCGCAGGCCACCACACCTGCTGTATTTTGTATTTTTAATAGAGATGCGGTTTCA T C CCNE2 Ensembl:ENSG00000175305 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1043820491 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_253214,RMVar_hsa_circ_53725,RMVar_hsa_circ_79006,RMVar_hsa_circ_315486,RMVar_hsa_circ_253215 50983 RMVar_ID_50983 Human_SNP_ID_373815269 A-to-I Human chr8 + 94902962 94902962 94902962 CTGACATCAGGTGATCCACCTGCCTCGGCCTCAAAGTGCTGGGATTACAGGCGTGAGCCACTGTG CTGACATCAGGTGATCCACCTGCCTCGGCCTCGAAGTGCTGGGATTACAGGCGTGAGCCACTGTG A G NDUFAF6 Ensembl:ENSG00000156170 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs906121521 Functional Loss SNV dbSNP153 33..33 33 - - - 50984 RMVar_ID_50984 Human_SNP_ID_373834978 A-to-I Human chr8 + 94983404 94983404 94983404 CTCCTGTCTCAGCCTCCTGAGTAGCTGGGATTACAGGTGTGCGCCACCACTGCCTGGCTAATTTT CTCCTGTCTCAGCCTCCTGAGTAGCTGGGATTGCAGGTGTGCGCCACCACTGCCTGGCTAATTTT A G NDUFAF6 Ensembl:ENSG00000156170 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1485544687 Functional Loss SNV dbSNP153 33..33 33 - - - 50985 RMVar_ID_50985 Human_SNP_ID_373835005 A-to-I Human chr8 + 94983527 94983527 94983527 ACCTCAAGTGATCCACCCGCCTCGGCCTCCCAAAGTGCTAGGATTTACAGGCATGAGCCACCACA ACCTCAAGTGATCCACCCGCCTCGGCCTCCCAGAGTGCTAGGATTTACAGGCATGAGCCACCACA A G NDUFAF6 Ensembl:ENSG00000156170 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs774692654 Functional Loss SNV dbSNP153 33..33 33 - - - 50986 RMVar_ID_50986 Human_SNP_ID_373835009 A-to-I Human chr8 + 94983547 94983547 94983547 CTCGGCCTCCCAAAGTGCTAGGATTTACAGGCATGAGCCACCACATCCAGCCAATTTTTCTTAAA CTCGGCCTCCCAAAGTGCTAGGATTTACAGGCGTGAGCCACCACATCCAGCCAATTTTTCTTAAA A G NDUFAF6 Ensembl:ENSG00000156170 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1219494357 Functional Loss SNV dbSNP153 33..33 33 - - - 50987 RMVar_ID_50987 Human_SNP_ID_373850122 A-to-I Human chr8 + 95048071 95048071 95048071 CAAAAATTAGCTGGGTGTGTTGGTGCACACCTATAGTCCCAGCTACTCAGGAGGCCAAGGTGGGA CAAAAATTAGCTGGGTGTGTTGGTGCACACCTGTAGTCCCAGCTACTCAGGAGGCCAAGGTGGGA A G NDUFAF6 Ensembl:ENSG00000156170 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs554168145 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_253221,RMVar_hsa_circ_109215,RMVar_hsa_circ_300382,RMVar_hsa_circ_288756,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_327074,RMVar_hsa_circ_364146,RMVar_hsa_circ_12699,RMVar_hsa_circ_125495,RMVar_hsa_circ_253228,RMVar_hsa_circ_253229,RMVar_hsa_circ_253231,RMVar_hsa_circ_280920,RMVar_hsa_circ_340151,RMVar_hsa_circ_76871,RMVar_hsa_circ_311221,RMVar_hsa_circ_253232 50988 RMVar_ID_50988 Human_SNP_ID_373852062 A-to-I Human chr8 + 95056427 95056427 95056427 GAGAGATGGGGTTTTGCCGTGATGCCCAGGCTAGTCTTGAACTCTTGAGCTCAAACAATCCACCT GAGAGATGGGGTTTTGCCGTGATGCCCAGGCTGGTCTTGAACTCTTGAGCTCAAACAATCCACCT A G NDUFAF6 Ensembl:ENSG00000156170 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs911870877 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_253221,RMVar_hsa_circ_109215,RMVar_hsa_circ_288756,RMVar_hsa_circ_253222,RMVar_hsa_circ_12699,RMVar_hsa_circ_253229,RMVar_hsa_circ_253231,RMVar_hsa_circ_76871 50989 RMVar_ID_50989 Human_SNP_ID_373852063 A-to-I Human chr8 + 95056427 95056427 95056427 GAGAGATGGGGTTTTGCCGTGATGCCCAGGCTAGTCTTGAACTCTTGAGCTCAAACAATCCACCT GAGAGATGGGGTTTTGCCGTGATGCCCAGGCTTGTCTTGAACTCTTGAGCTCAAACAATCCACCT A T NDUFAF6 Ensembl:ENSG00000156170 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs911870877 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_253221,RMVar_hsa_circ_109215,RMVar_hsa_circ_288756,RMVar_hsa_circ_253222,RMVar_hsa_circ_12699,RMVar_hsa_circ_253229,RMVar_hsa_circ_253231,RMVar_hsa_circ_76871 50990 RMVar_ID_50990 Human_SNP_ID_373896540 A-to-I Human chr8 - 95245556 95245556 95245556 TTTTGTATTTTTAATAGAGACAGGGTTTCACCATGTTGGCCAGAATGATGTCGATCTCCTGAACT TTTTGTATTTTTAATAGAGACAGGGTTTCACCGTGTTGGCCAGAATGATGTCGATCTCCTGAACT T C C8orf37 Ensembl:ENSG00000156172 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1383827903 Functional Loss SNV dbSNP153 33..33 33 - - - 50991 RMVar_ID_50991 Human_SNP_ID_373896584 A-to-I Human chr8 - 95245724 95245724 95245724 AAAAAAAAATTTTTTTTTTGAGATGGAGTGTCACTCTGTTGCCGGGCTGGAGTGCAGTGGCACGA AAAAAAAAATTTTTTTTTTGAGATGGAGTGTCGCTCTGTTGCCGGGCTGGAGTGCAGTGGCACGA T C C8orf37 Ensembl:ENSG00000156172 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1274364752 Functional Loss SNV dbSNP153 33..33 33 - - - 50992 RMVar_ID_50992 Human_SNP_ID_373896700 A-to-I Human chr8 - 95246126 95246126 95246126 AAATTAGCTGGGCGCGGTGGTGCATGCCTGTAATCCCAACTACTCGGGAGGCCGAGGCAGGAAAA AAATTAGCTGGGCGCGGTGGTGCATGCCTGTAGTCCCAACTACTCGGGAGGCCGAGGCAGGAAAA T C C8orf37 Ensembl:ENSG00000156172 Protein coding 3'UTR GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs995215831 Functional Loss SNV dbSNP153 33..33 33 - - - 50993 RMVar_ID_50993 Human_SNP_ID_373896704 A-to-I Human chr8 - 95246135 95246135 95246135 AAAATACAAAAATTAGCTGGGCGCGGTGGTGCATGCCTGTAATCCCAACTACTCGGGAGGCCGAG AAAATACAAAAATTAGCTGGGCGCGGTGGTGCGTGCCTGTAATCCCAACTACTCGGGAGGCCGAG T C C8orf37 Ensembl:ENSG00000156172 Protein coding 3'UTR GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1328594318 Functional Loss SNV dbSNP153 33..33 33 - - - 50994 RMVar_ID_50994 Human_SNP_ID_374153296 A-to-I Human chr8 + 96310423 96310423 96310423 TGACCTCATGATCTGACCCCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCAC TGACCTCATGATCTGACCCCCTTGGCCTCCCAGAGTGCTGGGATTACAGGCATGAGCCACCGCAC A G PTDSS1 Ensembl:ENSG00000156471 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1420336826 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16498713 RMVar_hsa_circ_73857,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_25539,RMVar_hsa_circ_91471,RMVar_hsa_circ_253245,RMVar_hsa_circ_296662,RMVar_hsa_circ_118639,RMVar_hsa_circ_253249,RMVar_hsa_circ_370562,RMVar_hsa_circ_125021,RMVar_hsa_circ_253252,RMVar_hsa_circ_253253,RMVar_hsa_circ_375690,RMVar_hsa_circ_253255,RMVar_hsa_circ_39860,RMVar_hsa_circ_286136,RMVar_hsa_circ_253254,RMVar_hsa_circ_253260,RMVar_hsa_circ_87308,RMVar_hsa_circ_253262,RMVar_hsa_circ_85405,RMVar_hsa_circ_253263,RMVar_hsa_circ_253261,RMVar_hsa_circ_253264,RMVar_hsa_circ_326275 50995 RMVar_ID_50995 Human_SNP_ID_374154175 A-to-I Human chr8 + 96314184 96314184 96314184 CTCCCACATCAGCCTCCTAAGTAGCTGGGACTATAGGCACACACCACAATGTCCAGCTAATTATA CTCCCACATCAGCCTCCTAAGTAGCTGGGACTGTAGGCACACACCACAATGTCCAGCTAATTATA A G PTDSS1 Ensembl:ENSG00000156471 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1247838700 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_73857,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_25539,RMVar_hsa_circ_91471,RMVar_hsa_circ_253245,RMVar_hsa_circ_296662,RMVar_hsa_circ_118639,RMVar_hsa_circ_253249,RMVar_hsa_circ_370562,RMVar_hsa_circ_125021,RMVar_hsa_circ_253252,RMVar_hsa_circ_253253,RMVar_hsa_circ_375690,RMVar_hsa_circ_253255,RMVar_hsa_circ_39860,RMVar_hsa_circ_286136,RMVar_hsa_circ_253254,RMVar_hsa_circ_253260,RMVar_hsa_circ_87308,RMVar_hsa_circ_253262,RMVar_hsa_circ_85405,RMVar_hsa_circ_253263,RMVar_hsa_circ_253261,RMVar_hsa_circ_253264,RMVar_hsa_circ_326275 50996 RMVar_ID_50996 Human_SNP_ID_374197247 A-to-I Human chr8 + 96500644 96500643 96500645 AGATCATGCCATGGCACTGCAGCCTGGGCGACAGAGTGAGACTCCATCTCAAAAAAAAAAAAAAA AGATCATGCCATGGCACTGCAGCCTGGGCGAC__AGTGAGACTCCATCTCAAAAAAAAAAAAAAA CAG C SDC2 Ensembl:ENSG00000169439 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1331854255 Functional Loss DEL dbSNP153 33..34 33 - - - 50997 RMVar_ID_50997 Human_SNP_ID_374197521 A-to-I Human chr8 + 96501434 96501434 96501434 TCAAGTGAATCTCCTGCCTCAACCTCCCGAGTAGCTGGGATTACAGTGCACACCACCACGCCTGG TCAAGTGAATCTCCTGCCTCAACCTCCCGAGTGGCTGGGATTACAGTGCACACCACCACGCCTGG A G SDC2 Ensembl:ENSG00000169439 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1276713101 Functional Loss SNV dbSNP153 33..33 33 - - - 50998 RMVar_ID_50998 Human_SNP_ID_374462616 A-to-I Human chr8 + 97647893 97647893 97647893 TTGAGCCTAGGAGTTTGACGCTGTGATGAGCTATGATCAGGTGACTGCACTCCAGCCTGGGCAAC TTGAGCCTAGGAGTTTGACGCTGTGATGAGCTGTGATCAGGTGACTGCACTCCAGCCTGGGCAAC A G MTDH Ensembl:ENSG00000147649 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968953435 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16499296 RMVar_hsa_circ_76057,RMVar_hsa_circ_253286 50999 RMVar_ID_50999 Human_SNP_ID_374463234 A-to-I Human chr8 + 97650387 97650387 97650387 ACCTCAACCTCCCAGGCTCAAGCGACTCTCCCACCTCAGCCTCCTGAGTAGCTGGGACTACAGAC ACCTCAACCTCCCAGGCTCAAGCGACTCTCCCGCCTCAGCCTCCTGAGTAGCTGGGACTACAGAC A G MTDH Ensembl:ENSG00000147649 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1429064531 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76057,RMVar_hsa_circ_253286 51000 RMVar_ID_51000 Human_SNP_ID_374464954 A-to-I Human chr8 + 97657708 97657708 97657708 TAAATTATTTTTTGTAGAGACAGGGTCTGTCTATGTTACTTGGGCTGGTCTCGAACTTCTGAGCT TAAATTATTTTTTGTAGAGACAGGGTCTGTCTGTGTTACTTGGGCTGGTCTCGAACTTCTGAGCT A G MTDH Ensembl:ENSG00000147649 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs78336506 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76057,RMVar_hsa_circ_253286 51001 RMVar_ID_51001 Human_SNP_ID_374466864 A-to-I Human chr8 + 97664891 97664891 97664891 CAAACAATTCTCCTGCCTCAGCCTCCTGAACCACTGGGATTATAGGCACGCACCACCACGCCCAG CAAACAATTCTCCTGCCTCAGCCTCCTGAACCCCTGGGATTATAGGCACGCACCACCACGCCCAG A C MTDH Ensembl:ENSG00000147649 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1214513418 Functional Loss SNV dbSNP153 33..33 33 - - - 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 51002 RMVar_ID_51002 Human_SNP_ID_374466873 A-to-I Human chr8 + 97664922 97664922 97664922 CACTGGGATTATAGGCACGCACCACCACGCCCAGCTATTTTTTGTATTTTTAGTAGAGACGGGGT CACTGGGATTATAGGCACGCACCACCACGCCCGGCTATTTTTTGTATTTTTAGTAGAGACGGGGT A G MTDH Ensembl:ENSG00000147649 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1005884340 Functional Loss SNV dbSNP153 33..33 33 - - - 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 51003 RMVar_ID_51003 Human_SNP_ID_374466876 A-to-I Human chr8 + 97664926 97664926 97664926 GGGATTATAGGCACGCACCACCACGCCCAGCTATTTTTTGTATTTTTAGTAGAGACGGGGTTTCA GGGATTATAGGCACGCACCACCACGCCCAGCTGTTTTTTGTATTTTTAGTAGAGACGGGGTTTCA A G MTDH Ensembl:ENSG00000147649 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs894821482 Functional Loss SNV dbSNP153 33..33 33 - - - 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 51004 RMVar_ID_51004 Human_SNP_ID_374466893 A-to-I Human chr8 + 97664996 97664996 97664996 TTGACCAAGGCTGGTCGCGAACTCCTGACCTCAGGTGATCTGCCTGCCTCGGCCTCCTAAAGTGC TTGACCAAGGCTGGTCGCGAACTCCTGACCTCGGGTGATCTGCCTGCCTCGGCCTCCTAAAGTGC A G MTDH Ensembl:ENSG00000147649 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs568380118 Functional Loss SNV dbSNP153 33..33 33 - - - 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 51005 RMVar_ID_51005 Human_SNP_ID_374468057 A-to-I Human chr8 + 97669249 97669249 97669249 CCGCTCACTGCAACCTCCACCTCCCTGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCTAGTAGC CCGCTCACTGCAACCTCCACCTCCCTGGGTTCCAGCAATTCTCCTGCCTCAGCCTCCCTAGTAGC A C MTDH Ensembl:ENSG00000147649 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1004173554 Functional Loss SNV dbSNP153 33..33 33 - - - 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 51006 RMVar_ID_51006 Human_SNP_ID_374468059 A-to-I Human chr8 + 97669253 97669253 97669253 TCACTGCAACCTCCACCTCCCTGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCTAGTAGCTGGG TCACTGCAACCTCCACCTCCCTGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCTAGTAGCTGGG A G MTDH Ensembl:ENSG00000147649 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs199930382 Functional Loss SNV dbSNP153 33..33 33 - - - 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 51007 RMVar_ID_51007 Human_SNP_ID_374468218 A-to-I Human chr8 + 97669795 97669795 97669795 AAAATTAGCTGGGCATGATGGCACACGCCTGTAATCCCAGCTATTTGGGAGGGTGAGGCAGGAGA AAAATTAGCTGGGCATGATGGCACACGCCTGTGATCCCAGCTATTTGGGAGGGTGAGGCAGGAGA A G MTDH Ensembl:ENSG00000147649 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1479659345 Functional Loss SNV dbSNP153 33..33 33 - - - 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 51008 RMVar_ID_51008 Human_SNP_ID_374468337 A-to-I Human chr8 + 97670195 97670195 97670195 AAATTAGCCAGGCACGGTGGCACGCCGCCTGTAGTCCCAGCTATTTGGGAGGCTGAGGTGGGAGA AAATTAGCCAGGCACGGTGGCACGCCGCCTGTGGTCCCAGCTATTTGGGAGGCTGAGGTGGGAGA A G MTDH Ensembl:ENSG00000147649 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs933061543 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8692540 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 51009 RMVar_ID_51009 Human_SNP_ID_374468429 A-to-I Human chr8 + 97670525 97670524 97670526 GTGCCCGTATAATCCCAGCCACTTGGGAGGCTAAGTCACGAGAATCACTTTAACCCAGGAGGTGG GTGCCCGTATAATCCCAGCCACTTGGGAGGCT__GTCACGAGAATCACTTTAACCCAGGAGGTGG TAA T MTDH Ensembl:ENSG00000147649 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1269751239 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_16499714 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 51010 RMVar_ID_51010 Human_SNP_ID_374468523 A-to-I Human chr8 + 97670886 97670886 97670886 TCGAGTGATTCTCCTGCCTCAGCCCCCCGAGTAACTGGGATTACAGGCGCCCACTGCCACGCCTG TCGAGTGATTCTCCTGCCTCAGCCCCCCGAGTGACTGGGATTACAGGCGCCCACTGCCACGCCTG A G MTDH Ensembl:ENSG00000147649 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs530856663 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26187601 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 51011 RMVar_ID_51011 Human_SNP_ID_374468526 A-to-I Human chr8 + 97670898 97670898 97670898 CCTGCCTCAGCCCCCCGAGTAACTGGGATTACAGGCGCCCACTGCCACGCCTGGCTAATTTTTTT CCTGCCTCAGCCCCCCGAGTAACTGGGATTACGGGCGCCCACTGCCACGCCTGGCTAATTTTTTT A G MTDH Ensembl:ENSG00000147649 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1401417389 Functional Loss SNV dbSNP153 33..33 33 - - - 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 51012 RMVar_ID_51012 Human_SNP_ID_374468846 A-to-I Human chr8 + 97671712 97671712 97671712 TAAAAATACAAAAATTAGCTTGGCATGGTGGTACGTGCCTGTAGTCCCAGCTACTTGGGAGGCTG TAAAAATACAAAAATTAGCTTGGCATGGTGGTGCGTGCCTGTAGTCCCAGCTACTTGGGAGGCTG A G MTDH Ensembl:ENSG00000147649 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1384118817 Functional Loss SNV dbSNP153 33..33 33 - - - 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 51013 RMVar_ID_51013 Human_SNP_ID_374469677 A-to-I Human chr8 + 97674928 97674928 97674928 GCCCTCCCGGGCTCAAGTGATTCTCCCACCTCAGCTTCCCAAGTAGCTGGGACTACAGGCATGCA GCCCTCCCGGGCTCAAGTGATTCTCCCACCTCGGCTTCCCAAGTAGCTGGGACTACAGGCATGCA A G MTDH Ensembl:ENSG00000147649 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs914844776 Functional Loss SNV dbSNP153 33..33 33 - - - 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 51014 RMVar_ID_51014 Human_SNP_ID_374469762 A-to-I Human chr8 + 97675305 97675305 97675305 ATTCAGGGCTGAGCACAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGTAG ATTCAGGGCTGAGCACAGTGGCTCACACCTGTGATCCCAGCACTTTGGGAGGCTGAGGTGGGTAG A G MTDH Ensembl:ENSG00000147649 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1244953272 Functional Loss SNV dbSNP153 33..33 33 - - - 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 51015 RMVar_ID_51015 Human_SNP_ID_374469910 A-to-I Human chr8 + 97675751 97675751 97675751 AAAATTAGCCTGGTGTGGTAGCGTATGCCTGTAGTCCCAGCTCCTTCGGAGGCTGAGGTGAGAGG AAAATTAGCCTGGTGTGGTAGCGTATGCCTGTGGTCCCAGCTCCTTCGGAGGCTGAGGTGAGAGG A G MTDH Ensembl:ENSG00000147649 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs939829972 Functional Loss SNV dbSNP153 33..33 33 - - - 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 51016 RMVar_ID_51016 Human_SNP_ID_374471200 A-to-I Human chr8 + 97680206 97680206 97680206 GTGATCCTCCCACCTCAGTCTGCCGAGTAGCTAGGACTACAGGTGTGCACCACCATGCCCAGCTA GTGATCCTCCCACCTCAGTCTGCCGAGTAGCTGGGACTACAGGTGTGCACCACCATGCCCAGCTA A G MTDH Ensembl:ENSG00000147649 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1398673721 Functional Loss SNV dbSNP153 33..33 33 - - - 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 51017 RMVar_ID_51017 Human_SNP_ID_374471203 A-to-I Human chr8 + 97680212 97680212 97680212 CTCCCACCTCAGTCTGCCGAGTAGCTAGGACTACAGGTGTGCACCACCATGCCCAGCTAATTTTT CTCCCACCTCAGTCTGCCGAGTAGCTAGGACTGCAGGTGTGCACCACCATGCCCAGCTAATTTTT A G MTDH Ensembl:ENSG00000147649 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1457908863 Functional Loss SNV dbSNP153 33..33 33 - - - 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 51018 RMVar_ID_51018 Human_SNP_ID_374471228 A-to-I Human chr8 + 97680292 97680292 97680292 CACAGTTTTGCCGTGTTGCCCAGGCTGGTCTCAAACTCCTGGCCTCAATCGGTCGGCCCACCTCA CACAGTTTTGCCGTGTTGCCCAGGCTGGTCTCGAACTCCTGGCCTCAATCGGTCGGCCCACCTCA A G MTDH Ensembl:ENSG00000147649 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1476062072 Functional Loss SNV dbSNP153 33..33 33 - - - 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 51019 RMVar_ID_51019 Human_SNP_ID_374471566 A-to-I Human chr8 + 97681623 97681623 97681623 TCAAGCGATTCTTCTGCCTCAGCCTCCCGAGTAGCTGTGATTACAGGCATGCACCAGCACGCTTG TCAAGCGATTCTTCTGCCTCAGCCTCCCGAGTGGCTGTGATTACAGGCATGCACCAGCACGCTTG A G MTDH Ensembl:ENSG00000147649 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs537803712 Functional Loss SNV dbSNP153 33..33 33 - - - 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 51020 RMVar_ID_51020 Human_SNP_ID_374472420 A-to-I Human chr8 + 97684089 97684089 97684089 AACCCAGGCGGCAGAGGTTGCGGTGAACTGAGATCGCGCCATTGCACTCCAGCCTGGGCAACAAG AACCCAGGCGGCAGAGGTTGCGGTGAACTGAGGTCGCGCCATTGCACTCCAGCCTGGGCAACAAG A G MTDH Ensembl:ENSG00000147649 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs191369549 Functional Loss SNV dbSNP153 33..33 33 - - - 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 51021 RMVar_ID_51021 Human_SNP_ID_374475116 A-to-I Human chr8 + 97694275 97694275 97694275 GCTGGAGTGCAATGGCACGATCTCGGCTCACCACAACCACCGCCTCTCGGGTTCAAGCAATTCTC GCTGGAGTGCAATGGCACGATCTCGGCTCACCGCAACCACCGCCTCTCGGGTTCAAGCAATTCTC A G MTDH Ensembl:ENSG00000147649 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1191753113 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69358,RMVar_hsa_circ_76057,RMVar_hsa_circ_253286,RMVar_hsa_circ_292754,RMVar_hsa_circ_98877,RMVar_hsa_circ_253288,RMVar_hsa_circ_253290,RMVar_hsa_circ_253289,RMVar_hsa_circ_253295,RMVar_hsa_circ_341218,RMVar_hsa_circ_366544,RMVar_hsa_circ_367157,RMVar_hsa_circ_325314,RMVar_hsa_circ_289793,RMVar_hsa_circ_253296,RMVar_hsa_circ_96623,RMVar_hsa_circ_253299,RMVar_hsa_circ_64711,RMVar_hsa_circ_320821,RMVar_hsa_circ_45496,RMVar_hsa_circ_92978,RMVar_hsa_circ_253297,RMVar_hsa_circ_61908,RMVar_hsa_circ_253298,RMVar_hsa_circ_330312,RMVar_hsa_circ_125725,RMVar_hsa_circ_305474,RMVar_hsa_circ_93704,RMVar_hsa_circ_253301,RMVar_hsa_circ_253303,RMVar_hsa_circ_253302,RMVar_hsa_circ_253300 51022 RMVar_ID_51022 Human_SNP_ID_374475208 A-to-I Human chr8 + 97694666 97694666 97694666 TCCCTTGCCTGGGCATGGTGGCTCATGTCTGTAATCCTGGCACTTTGCAGGGCTGAGGCTGGCAG TCCCTTGCCTGGGCATGGTGGCTCATGTCTGTGATCCTGGCACTTTGCAGGGCTGAGGCTGGCAG A G MTDH Ensembl:ENSG00000147649 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs908080151 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69358,RMVar_hsa_circ_76057,RMVar_hsa_circ_253286,RMVar_hsa_circ_292754,RMVar_hsa_circ_98877,RMVar_hsa_circ_253288,RMVar_hsa_circ_253290,RMVar_hsa_circ_253289,RMVar_hsa_circ_253295,RMVar_hsa_circ_341218,RMVar_hsa_circ_366544,RMVar_hsa_circ_367157,RMVar_hsa_circ_325314,RMVar_hsa_circ_289793,RMVar_hsa_circ_253296,RMVar_hsa_circ_96623,RMVar_hsa_circ_253299,RMVar_hsa_circ_64711,RMVar_hsa_circ_320821,RMVar_hsa_circ_45496,RMVar_hsa_circ_92978,RMVar_hsa_circ_253297,RMVar_hsa_circ_61908,RMVar_hsa_circ_253298,RMVar_hsa_circ_330312,RMVar_hsa_circ_125725,RMVar_hsa_circ_305474,RMVar_hsa_circ_93704,RMVar_hsa_circ_253301,RMVar_hsa_circ_253303,RMVar_hsa_circ_253302,RMVar_hsa_circ_253300 51023 RMVar_ID_51023 Human_SNP_ID_374475269 A-to-I Human chr8 + 97694864 97694864 97694864 ACAATTGCTTAAACCTGGGAAGCGGAGATTGCAGTGAGCCAAGGTCGAGCCACTGCACTCCAGCC ACAATTGCTTAAACCTGGGAAGCGGAGATTGCTGTGAGCCAAGGTCGAGCCACTGCACTCCAGCC A T MTDH Ensembl:ENSG00000147649 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1260152273 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69358,RMVar_hsa_circ_76057,RMVar_hsa_circ_253286,RMVar_hsa_circ_292754,RMVar_hsa_circ_98877,RMVar_hsa_circ_253288,RMVar_hsa_circ_253290,RMVar_hsa_circ_253289,RMVar_hsa_circ_253295,RMVar_hsa_circ_341218,RMVar_hsa_circ_366544,RMVar_hsa_circ_367157,RMVar_hsa_circ_325314,RMVar_hsa_circ_289793,RMVar_hsa_circ_253296,RMVar_hsa_circ_96623,RMVar_hsa_circ_253299,RMVar_hsa_circ_64711,RMVar_hsa_circ_320821,RMVar_hsa_circ_45496,RMVar_hsa_circ_92978,RMVar_hsa_circ_253297,RMVar_hsa_circ_61908,RMVar_hsa_circ_253298,RMVar_hsa_circ_330312,RMVar_hsa_circ_125725,RMVar_hsa_circ_305474,RMVar_hsa_circ_93704,RMVar_hsa_circ_253301,RMVar_hsa_circ_253303,RMVar_hsa_circ_253302,RMVar_hsa_circ_253300 51024 RMVar_ID_51024 Human_SNP_ID_374475279 A-to-I Human chr8 + 97694902 97694902 97694902 CCAAGGTCGAGCCACTGCACTCCAGCCTTGGCAACAGAGCGAGACTCCCTCTCAAAAAGAAAAAA CCAAGGTCGAGCCACTGCACTCCAGCCTTGGCTACAGAGCGAGACTCCCTCTCAAAAAGAAAAAA A T MTDH Ensembl:ENSG00000147649 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1401832323 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69358,RMVar_hsa_circ_76057,RMVar_hsa_circ_253286,RMVar_hsa_circ_292754,RMVar_hsa_circ_98877,RMVar_hsa_circ_253288,RMVar_hsa_circ_253290,RMVar_hsa_circ_253289,RMVar_hsa_circ_253295,RMVar_hsa_circ_341218,RMVar_hsa_circ_366544,RMVar_hsa_circ_367157,RMVar_hsa_circ_325314,RMVar_hsa_circ_289793,RMVar_hsa_circ_253296,RMVar_hsa_circ_96623,RMVar_hsa_circ_253299,RMVar_hsa_circ_64711,RMVar_hsa_circ_320821,RMVar_hsa_circ_45496,RMVar_hsa_circ_92978,RMVar_hsa_circ_253297,RMVar_hsa_circ_61908,RMVar_hsa_circ_253298,RMVar_hsa_circ_330312,RMVar_hsa_circ_125725,RMVar_hsa_circ_305474,RMVar_hsa_circ_93704,RMVar_hsa_circ_253301,RMVar_hsa_circ_253303,RMVar_hsa_circ_253302,RMVar_hsa_circ_253300 51025 RMVar_ID_51025 Human_SNP_ID_374476500 A-to-I Human chr8 + 97699070 97699070 97699070 CACTTTGGGAGGCTGAGGCAGGAGGATCACTTAAGCCTAGGAGTTCAAGACCAGCCTGGGCAACA CACTTTGGGAGGCTGAGGCAGGAGGATCACTTGAGCCTAGGAGTTCAAGACCAGCCTGGGCAACA A G MTDH Ensembl:ENSG00000147649 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2917958 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69358,RMVar_hsa_circ_76057,RMVar_hsa_circ_253286,RMVar_hsa_circ_292754,RMVar_hsa_circ_98877,RMVar_hsa_circ_253288,RMVar_hsa_circ_253289,RMVar_hsa_circ_341218,RMVar_hsa_circ_366544,RMVar_hsa_circ_367157,RMVar_hsa_circ_325314,RMVar_hsa_circ_289793,RMVar_hsa_circ_253296,RMVar_hsa_circ_96623,RMVar_hsa_circ_253299,RMVar_hsa_circ_64711,RMVar_hsa_circ_320821,RMVar_hsa_circ_45496,RMVar_hsa_circ_92978,RMVar_hsa_circ_253297,RMVar_hsa_circ_61908,RMVar_hsa_circ_253298,RMVar_hsa_circ_330312,RMVar_hsa_circ_125725,RMVar_hsa_circ_305474,RMVar_hsa_circ_93704,RMVar_hsa_circ_253301,RMVar_hsa_circ_253302,RMVar_hsa_circ_253300 51026 RMVar_ID_51026 Human_SNP_ID_374476514 A-to-I Human chr8 + 97699123 97699123 97699123 GCCTGGGCAACATGGTGTAAAACCCCATCTCTACAAAAAATACAAAAATTAGCTGGGTATGGTAA GCCTGGGCAACATGGTGTAAAACCCCATCTCTGCAAAAAATACAAAAATTAGCTGGGTATGGTAA A G MTDH Ensembl:ENSG00000147649 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1160552598 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69358,RMVar_hsa_circ_76057,RMVar_hsa_circ_253286,RMVar_hsa_circ_292754,RMVar_hsa_circ_98877,RMVar_hsa_circ_253288,RMVar_hsa_circ_253289,RMVar_hsa_circ_341218,RMVar_hsa_circ_366544,RMVar_hsa_circ_367157,RMVar_hsa_circ_325314,RMVar_hsa_circ_289793,RMVar_hsa_circ_253296,RMVar_hsa_circ_96623,RMVar_hsa_circ_253299,RMVar_hsa_circ_64711,RMVar_hsa_circ_320821,RMVar_hsa_circ_45496,RMVar_hsa_circ_92978,RMVar_hsa_circ_253297,RMVar_hsa_circ_61908,RMVar_hsa_circ_253298,RMVar_hsa_circ_330312,RMVar_hsa_circ_125725,RMVar_hsa_circ_305474,RMVar_hsa_circ_93704,RMVar_hsa_circ_253301,RMVar_hsa_circ_253302,RMVar_hsa_circ_253300 51027 RMVar_ID_51027 Human_SNP_ID_374478341 A-to-I Human chr8 + 97706822 97706822 97706822 AAGAGACAGGCTGGGCACAGTGGCTCACGCCTATGATTCCAGCACTTTGGGAGGTACTGTGGGAG AAGAGACAGGCTGGGCACAGTGGCTCACGCCTGTGATTCCAGCACTTTGGGAGGTACTGTGGGAG A G MTDH Ensembl:ENSG00000147649 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1214394833 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69358,RMVar_hsa_circ_341218,RMVar_hsa_circ_366544,RMVar_hsa_circ_367157,RMVar_hsa_circ_253299,RMVar_hsa_circ_64711,RMVar_hsa_circ_320821,RMVar_hsa_circ_45496,RMVar_hsa_circ_61908,RMVar_hsa_circ_305474,RMVar_hsa_circ_93704,RMVar_hsa_circ_253301,RMVar_hsa_circ_253300,RMVar_hsa_circ_253306,RMVar_hsa_circ_253308,RMVar_hsa_circ_294717,RMVar_hsa_circ_314005,RMVar_hsa_circ_319909,RMVar_hsa_circ_113280,RMVar_hsa_circ_253307,RMVar_hsa_circ_253310,RMVar_hsa_circ_291386,RMVar_hsa_circ_352894,RMVar_hsa_circ_315212,RMVar_hsa_circ_267391,RMVar_hsa_circ_253309 51028 RMVar_ID_51028 Human_SNP_ID_374478927 A-to-I Human chr8 + 97708679 97708679 97708679 TGGAGTGCAGTGGCATGATCTCGGCTCTCTGCAACCTCCACCTCCCAGGTTCAAGTGATTCTCCC TGGAGTGCAGTGGCATGATCTCGGCTCTCTGCGACCTCCACCTCCCAGGTTCAAGTGATTCTCCC A G MTDH Ensembl:ENSG00000147649 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1457974050 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69358,RMVar_hsa_circ_341218,RMVar_hsa_circ_366544,RMVar_hsa_circ_367157,RMVar_hsa_circ_253299,RMVar_hsa_circ_64711,RMVar_hsa_circ_320821,RMVar_hsa_circ_45496,RMVar_hsa_circ_61908,RMVar_hsa_circ_305474,RMVar_hsa_circ_93704,RMVar_hsa_circ_253301,RMVar_hsa_circ_253300,RMVar_hsa_circ_253306,RMVar_hsa_circ_253308,RMVar_hsa_circ_294717,RMVar_hsa_circ_314005,RMVar_hsa_circ_319909,RMVar_hsa_circ_113280,RMVar_hsa_circ_253307,RMVar_hsa_circ_253310,RMVar_hsa_circ_291386,RMVar_hsa_circ_352894,RMVar_hsa_circ_315212,RMVar_hsa_circ_267391,RMVar_hsa_circ_253309 51029 RMVar_ID_51029 Human_SNP_ID_374478930 A-to-I Human chr8 + 97708686 97708686 97708686 CAGTGGCATGATCTCGGCTCTCTGCAACCTCCACCTCCCAGGTTCAAGTGATTCTCCCTCCTCAG CAGTGGCATGATCTCGGCTCTCTGCAACCTCCCCCTCCCAGGTTCAAGTGATTCTCCCTCCTCAG A C MTDH Ensembl:ENSG00000147649 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1387523695 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69358,RMVar_hsa_circ_341218,RMVar_hsa_circ_366544,RMVar_hsa_circ_367157,RMVar_hsa_circ_253299,RMVar_hsa_circ_64711,RMVar_hsa_circ_320821,RMVar_hsa_circ_45496,RMVar_hsa_circ_61908,RMVar_hsa_circ_305474,RMVar_hsa_circ_93704,RMVar_hsa_circ_253301,RMVar_hsa_circ_253300,RMVar_hsa_circ_253306,RMVar_hsa_circ_253308,RMVar_hsa_circ_294717,RMVar_hsa_circ_314005,RMVar_hsa_circ_319909,RMVar_hsa_circ_113280,RMVar_hsa_circ_253307,RMVar_hsa_circ_253310,RMVar_hsa_circ_291386,RMVar_hsa_circ_352894,RMVar_hsa_circ_315212,RMVar_hsa_circ_267391,RMVar_hsa_circ_253309 51030 RMVar_ID_51030 Human_SNP_ID_374479007 A-to-I Human chr8 + 97708968 97708968 97708968 AGTGGCTCCCACTTTGCGAGGCCAAGGTGGGTAGATCACAAGGTCAGGAGTTCAAGACCAGCCGG AGTGGCTCCCACTTTGCGAGGCCAAGGTGGGTGGATCACAAGGTCAGGAGTTCAAGACCAGCCGG A G MTDH Ensembl:ENSG00000147649 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1194282363 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69358,RMVar_hsa_circ_341218,RMVar_hsa_circ_366544,RMVar_hsa_circ_367157,RMVar_hsa_circ_253299,RMVar_hsa_circ_64711,RMVar_hsa_circ_320821,RMVar_hsa_circ_45496,RMVar_hsa_circ_61908,RMVar_hsa_circ_305474,RMVar_hsa_circ_93704,RMVar_hsa_circ_253301,RMVar_hsa_circ_253300,RMVar_hsa_circ_253306,RMVar_hsa_circ_253308,RMVar_hsa_circ_294717,RMVar_hsa_circ_314005,RMVar_hsa_circ_319909,RMVar_hsa_circ_113280,RMVar_hsa_circ_253307,RMVar_hsa_circ_253310,RMVar_hsa_circ_291386,RMVar_hsa_circ_352894,RMVar_hsa_circ_315212,RMVar_hsa_circ_267391,RMVar_hsa_circ_253309 51031 RMVar_ID_51031 Human_SNP_ID_374479045 A-to-I Human chr8 + 97709143 97709143 97709143 TTGAACCCGGGAGGCAGAGGTTACAGTGAGCCAAGGTTGTGCCACTGCACTCCAGCCTGGACAAC TTGAACCCGGGAGGCAGAGGTTACAGTGAGCCGAGGTTGTGCCACTGCACTCCAGCCTGGACAAC A G MTDH Ensembl:ENSG00000147649 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1230600627 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69358,RMVar_hsa_circ_341218,RMVar_hsa_circ_366544,RMVar_hsa_circ_367157,RMVar_hsa_circ_253299,RMVar_hsa_circ_64711,RMVar_hsa_circ_320821,RMVar_hsa_circ_45496,RMVar_hsa_circ_61908,RMVar_hsa_circ_305474,RMVar_hsa_circ_93704,RMVar_hsa_circ_253301,RMVar_hsa_circ_253300,RMVar_hsa_circ_253306,RMVar_hsa_circ_253308,RMVar_hsa_circ_294717,RMVar_hsa_circ_314005,RMVar_hsa_circ_319909,RMVar_hsa_circ_113280,RMVar_hsa_circ_253307,RMVar_hsa_circ_253310,RMVar_hsa_circ_291386,RMVar_hsa_circ_352894,RMVar_hsa_circ_315212,RMVar_hsa_circ_267391,RMVar_hsa_circ_253309 51032 RMVar_ID_51032 Human_SNP_ID_374479486 A-to-I Human chr8 + 97710840 97710840 97710840 TGACCAACAAGGTGAAACCCCATCTCTACTGAAAATAGAAAAATTAGCCGGGCATGGTGGTGCAC TGACCAACAAGGTGAAACCCCATCTCTACTGAGAATAGAAAAATTAGCCGGGCATGGTGGTGCAC A G MTDH Ensembl:ENSG00000147649 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1349836868 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69358,RMVar_hsa_circ_341218,RMVar_hsa_circ_366544,RMVar_hsa_circ_367157,RMVar_hsa_circ_253299,RMVar_hsa_circ_64711,RMVar_hsa_circ_320821,RMVar_hsa_circ_45496,RMVar_hsa_circ_61908,RMVar_hsa_circ_305474,RMVar_hsa_circ_93704,RMVar_hsa_circ_253301,RMVar_hsa_circ_253300,RMVar_hsa_circ_253306,RMVar_hsa_circ_253308,RMVar_hsa_circ_294717,RMVar_hsa_circ_314005,RMVar_hsa_circ_319909,RMVar_hsa_circ_113280,RMVar_hsa_circ_253307,RMVar_hsa_circ_253310,RMVar_hsa_circ_291386,RMVar_hsa_circ_352894,RMVar_hsa_circ_315212,RMVar_hsa_circ_267391,RMVar_hsa_circ_253309 51033 RMVar_ID_51033 Human_SNP_ID_374479589 A-to-I Human chr8 + 97711269 97711269 97711269 CCTGTAATCCCAGCACTTTGGGAGACTAAGGTAGGAGGATCACTTGAGCCCATGGTGTTTGAGAC CCTGTAATCCCAGCACTTTGGGAGACTAAGGTGGGAGGATCACTTGAGCCCATGGTGTTTGAGAC A G MTDH Ensembl:ENSG00000147649 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1207821306 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18900832 RMVar_hsa_circ_69358,RMVar_hsa_circ_341218,RMVar_hsa_circ_366544,RMVar_hsa_circ_367157,RMVar_hsa_circ_253299,RMVar_hsa_circ_64711,RMVar_hsa_circ_320821,RMVar_hsa_circ_45496,RMVar_hsa_circ_61908,RMVar_hsa_circ_305474,RMVar_hsa_circ_93704,RMVar_hsa_circ_253301,RMVar_hsa_circ_253300,RMVar_hsa_circ_253306,RMVar_hsa_circ_253308,RMVar_hsa_circ_294717,RMVar_hsa_circ_314005,RMVar_hsa_circ_319909,RMVar_hsa_circ_113280,RMVar_hsa_circ_253307,RMVar_hsa_circ_253310,RMVar_hsa_circ_291386,RMVar_hsa_circ_352894,RMVar_hsa_circ_315212,RMVar_hsa_circ_267391,RMVar_hsa_circ_253309 51034 RMVar_ID_51034 Human_SNP_ID_374480366 A-to-I Human chr8 + 97714379 97714379 97714379 TCATGCCTGTAATCCCAGCACATTGGAAGGCTAAGGCAGGAGGATCACTTCAGTCCAGGAGCTTG TCATGCCTGTAATCCCAGCACATTGGAAGGCTGAGGCAGGAGGATCACTTCAGTCCAGGAGCTTG A G MTDH Ensembl:ENSG00000147649 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1463393608 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89898,RMVar_hsa_circ_341218,RMVar_hsa_circ_367157,RMVar_hsa_circ_253299,RMVar_hsa_circ_320821,RMVar_hsa_circ_61908,RMVar_hsa_circ_305474,RMVar_hsa_circ_93704,RMVar_hsa_circ_253301,RMVar_hsa_circ_253300,RMVar_hsa_circ_253308,RMVar_hsa_circ_294717,RMVar_hsa_circ_319909,RMVar_hsa_circ_113280,RMVar_hsa_circ_253307,RMVar_hsa_circ_253310,RMVar_hsa_circ_291386,RMVar_hsa_circ_352894,RMVar_hsa_circ_267391,RMVar_hsa_circ_290546,RMVar_hsa_circ_278420,RMVar_hsa_circ_253311,RMVar_hsa_circ_253313,RMVar_hsa_circ_253314,RMVar_hsa_circ_253312 51035 RMVar_ID_51035 Human_SNP_ID_374480523 A-to-I Human chr8 + 97714959 97714959 97714959 GCGATTCTCCTGCCTCAGCTTCCCAAGTAGCTAGGATTACAGGCATGTGCCACCACGCCTGGCTA GCGATTCTCCTGCCTCAGCTTCCCAAGTAGCTGGGATTACAGGCATGTGCCACCACGCCTGGCTA A G MTDH Ensembl:ENSG00000147649 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1009127135 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89898,RMVar_hsa_circ_341218,RMVar_hsa_circ_367157,RMVar_hsa_circ_253299,RMVar_hsa_circ_320821,RMVar_hsa_circ_61908,RMVar_hsa_circ_305474,RMVar_hsa_circ_93704,RMVar_hsa_circ_253301,RMVar_hsa_circ_253300,RMVar_hsa_circ_253308,RMVar_hsa_circ_294717,RMVar_hsa_circ_319909,RMVar_hsa_circ_113280,RMVar_hsa_circ_253307,RMVar_hsa_circ_253310,RMVar_hsa_circ_291386,RMVar_hsa_circ_352894,RMVar_hsa_circ_267391,RMVar_hsa_circ_290546,RMVar_hsa_circ_278420,RMVar_hsa_circ_253311,RMVar_hsa_circ_253313,RMVar_hsa_circ_253314,RMVar_hsa_circ_253312 51036 RMVar_ID_51036 Human_SNP_ID_374482169 A-to-I Human chr8 + 97721288 97721287 97721288 AATGATGAAACCCCCGTCTCTACCAAAAATACAAAAAAGTAACTGGATGTGGTGGTGTGCACCTG AATGATGAAACCCCCGTCTCTACCAAAAATAC_AAAAAGTAACTGGATGTGGTGGTGTGCACCTG CA C MTDH Ensembl:ENSG00000147649 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1183881786 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_89898,RMVar_hsa_circ_341218,RMVar_hsa_circ_253299,RMVar_hsa_circ_305474,RMVar_hsa_circ_93704,RMVar_hsa_circ_253300,RMVar_hsa_circ_253308,RMVar_hsa_circ_294717,RMVar_hsa_circ_113280,RMVar_hsa_circ_253307,RMVar_hsa_circ_352894,RMVar_hsa_circ_267391,RMVar_hsa_circ_278420,RMVar_hsa_circ_253311,RMVar_hsa_circ_253313,RMVar_hsa_circ_253312,RMVar_hsa_circ_291779,RMVar_hsa_circ_253316 51037 RMVar_ID_51037 Human_SNP_ID_374483635 A-to-I Human chr8 + 97726980 97726980 97726980 GGGCTCCTGTAATCCCAGCTACTCAGGAGGCTAAGGCAGAGAATCATTTGAACCCAGGAGACGGA GGGCTCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGAGAATCATTTGAACCCAGGAGACGGA A G MTDH Ensembl:ENSG00000147649 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1327269370 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7869273,Human_RBP_ID_16500378 RMVar_hsa_circ_89898,RMVar_hsa_circ_253299,RMVar_hsa_circ_93704,RMVar_hsa_circ_253308,RMVar_hsa_circ_113280,RMVar_hsa_circ_267391,RMVar_hsa_circ_126964,RMVar_hsa_circ_253311,RMVar_hsa_circ_83888,RMVar_hsa_circ_253317,RMVar_hsa_circ_253318 51038 RMVar_ID_51038 Human_SNP_ID_374483733 A-to-I Human chr8 + 97727366 97727363 97727366 TACAAAATTTGCAAAAAGTAGATGGGTGTGGTAGTGGGCGCCTGTAATCCCAGCTACTCAGGAGG TACAAAATTTGCAAAAAGTAGATGGGTGTG___GTGGGCGCCTGTAATCCCAGCTACTCAGGAGG GGTA G MTDH Ensembl:ENSG00000147649 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1228224516 Functional Loss DEL dbSNP153 31..33 33 - - - RMVar_hsa_circ_89898,RMVar_hsa_circ_253299,RMVar_hsa_circ_93704,RMVar_hsa_circ_253308,RMVar_hsa_circ_113280,RMVar_hsa_circ_267391,RMVar_hsa_circ_126964,RMVar_hsa_circ_253311,RMVar_hsa_circ_83888,RMVar_hsa_circ_253317,RMVar_hsa_circ_253318 51039 RMVar_ID_51039 Human_SNP_ID_374483734 A-to-I Human chr8 + 97727366 97727366 97727366 TACAAAATTTGCAAAAAGTAGATGGGTGTGGTAGTGGGCGCCTGTAATCCCAGCTACTCAGGAGG TACAAAATTTGCAAAAAGTAGATGGGTGTGGTGGTGGGCGCCTGTAATCCCAGCTACTCAGGAGG A G MTDH Ensembl:ENSG00000147649 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs974593458 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89898,RMVar_hsa_circ_253299,RMVar_hsa_circ_93704,RMVar_hsa_circ_253308,RMVar_hsa_circ_113280,RMVar_hsa_circ_267391,RMVar_hsa_circ_126964,RMVar_hsa_circ_253311,RMVar_hsa_circ_83888,RMVar_hsa_circ_253317,RMVar_hsa_circ_253318 51040 RMVar_ID_51040 Human_SNP_ID_374484154 A-to-I Human chr8 + 97728935 97728935 97728935 TGTAGCTTTTTTTTTTTTTCTTTTAATGAGATAGGGTCTCACTCTGTTGCCCAGGCTGGAGTGCA TGTAGCTTTTTTTTTTTTTCTTTTAATGAGATGGGGTCTCACTCTGTTGCCCAGGCTGGAGTGCA A G MTDH Ensembl:ENSG00000147649 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1305723263 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7869309 RMVar_hsa_circ_89898,RMVar_hsa_circ_253299,RMVar_hsa_circ_93704,RMVar_hsa_circ_253308,RMVar_hsa_circ_113280,RMVar_hsa_circ_267391,RMVar_hsa_circ_126964,RMVar_hsa_circ_253311,RMVar_hsa_circ_83888,RMVar_hsa_circ_253317,RMVar_hsa_circ_253318 51041 RMVar_ID_51041 Human_SNP_ID_374484186 A-to-I Human chr8 + 97729031 97729031 97729031 ACTCCCGGGCTCGAGCTATATTCTCCCACTTTAGCCTCAGCCTCCAGAGTACCTGGGACTACAGG ACTCCCGGGCTCGAGCTATATTCTCCCACTTTGGCCTCAGCCTCCAGAGTACCTGGGACTACAGG A G MTDH Ensembl:ENSG00000147649 Protein coding 3'UTR GSE38233;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,32596459 RNA-Seq:(High) rs1249964198 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89898,RMVar_hsa_circ_253299,RMVar_hsa_circ_93704,RMVar_hsa_circ_253308,RMVar_hsa_circ_113280,RMVar_hsa_circ_267391,RMVar_hsa_circ_126964,RMVar_hsa_circ_253311,RMVar_hsa_circ_83888,RMVar_hsa_circ_253317,RMVar_hsa_circ_253318 51042 RMVar_ID_51042 Human_SNP_ID_374484188 A-to-I Human chr8 + 97729037 97729037 97729037 GGGCTCGAGCTATATTCTCCCACTTTAGCCTCAGCCTCCAGAGTACCTGGGACTACAGGTACACA GGGCTCGAGCTATATTCTCCCACTTTAGCCTCCGCCTCCAGAGTACCTGGGACTACAGGTACACA A C MTDH Ensembl:ENSG00000147649 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1187265208 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89898,RMVar_hsa_circ_253299,RMVar_hsa_circ_93704,RMVar_hsa_circ_253308,RMVar_hsa_circ_113280,RMVar_hsa_circ_267391,RMVar_hsa_circ_126964,RMVar_hsa_circ_253311,RMVar_hsa_circ_83888,RMVar_hsa_circ_253317,RMVar_hsa_circ_253318 51043 RMVar_ID_51043 Human_SNP_ID_374484198 A-to-I Human chr8 + 97729085 97729084 97729085 GGGACTACAGGTACACACCACCATGCCTGGCTAAATTTTTTTTTTTTTTTTTTGGTAGAGATGAG GGGACTACAGGTACACACCACCATGCCTGGCT_AATTTTTTTTTTTTTTTTTTGGTAGAGATGAG TA T MTDH Ensembl:ENSG00000147649 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1207401170 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_7869312 RMVar_hsa_circ_89898,RMVar_hsa_circ_253299,RMVar_hsa_circ_93704,RMVar_hsa_circ_253308,RMVar_hsa_circ_113280,RMVar_hsa_circ_267391,RMVar_hsa_circ_126964,RMVar_hsa_circ_253311,RMVar_hsa_circ_83888,RMVar_hsa_circ_253317,RMVar_hsa_circ_253318 51044 RMVar_ID_51044 Human_SNP_ID_374484199 A-to-I Human chr8 + 97729085 97729085 97729085 GGGACTACAGGTACACACCACCATGCCTGGCTAAATTTTTTTTTTTTTTTTTTGGTAGAGATGAG GGGACTACAGGTACACACCACCATGCCTGGCTTAATTTTTTTTTTTTTTTTTTGGTAGAGATGAG A T MTDH Ensembl:ENSG00000147649 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs62521709 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7869312 RMVar_hsa_circ_89898,RMVar_hsa_circ_253299,RMVar_hsa_circ_93704,RMVar_hsa_circ_253308,RMVar_hsa_circ_113280,RMVar_hsa_circ_267391,RMVar_hsa_circ_126964,RMVar_hsa_circ_253311,RMVar_hsa_circ_83888,RMVar_hsa_circ_253317,RMVar_hsa_circ_253318 51045 RMVar_ID_51045 Human_SNP_ID_374484353 A-to-I Human chr8 + 97729686 97729685 97729687 TTGCTTTTTGTTTTTTGTTTTTTTCTAGAGACAGAGTCTCGTTGCCCAGGCTGGTCTCCAATTCC TTGCTTTTTGTTTTTTGTTTTTTTCTAGAGAC__AGTCTCGTTGCCCAGGCTGGTCTCCAATTCC CAG C MTDH Ensembl:ENSG00000147649 Protein coding 3'UTR GSE38233;GSE100210;GSE107867 cultured B-cells;HepG2 cell line;ASD brains,frontal_cortex - 24183664,29129909,30559470 RNA-Seq:(High) rs1288699463 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_7869321,Human_RBP_ID_16500398 RMVar_hsa_circ_89898,RMVar_hsa_circ_253299,RMVar_hsa_circ_93704,RMVar_hsa_circ_253308,RMVar_hsa_circ_113280,RMVar_hsa_circ_267391,RMVar_hsa_circ_126964,RMVar_hsa_circ_253311,RMVar_hsa_circ_83888,RMVar_hsa_circ_253317,RMVar_hsa_circ_253318 51046 RMVar_ID_51046 Human_SNP_ID_374484373 A-to-I Human chr8 + 97729765 97729765 97729765 CCTCCTGACTCAGCCTCCTAAATGCTGGGATTACAGGCATGAACCACTGTGCCCAGTCTATATAT CCTCCTGACTCAGCCTCCTAAATGCTGGGATTGCAGGCATGAACCACTGTGCCCAGTCTATATAT A G MTDH Ensembl:ENSG00000147649 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1045459 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_706647,Human_RBP_ID_22410615 Human_miRNA_ID_1995464,Human_miRNA_ID_2057709,Human_miRNA_ID_2227960,Human_miRNA_ID_2503940 RMVar_hsa_circ_89898,RMVar_hsa_circ_253299,RMVar_hsa_circ_93704,RMVar_hsa_circ_253308,RMVar_hsa_circ_113280,RMVar_hsa_circ_267391,RMVar_hsa_circ_126964,RMVar_hsa_circ_253311,RMVar_hsa_circ_83888,RMVar_hsa_circ_253317,RMVar_hsa_circ_253318 51047 RMVar_ID_51047 Human_SNP_ID_374516140 A-to-I Human chr8 + 97846397 97846397 97846397 GTTGCCCAGGCTGGAGTGCAATGCGCGATCTCAGCTCACCACAGCCACCGCCTCCCGGGTTCAAG GTTGCCCAGGCTGGAGTGCAATGCGCGATCTCGGCTCACCACAGCCACCGCCTCCCGGGTTCAAG A G LAPTM4B Ensembl:ENSG00000104341 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs550095090 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 51048 RMVar_ID_51048 Human_SNP_ID_374516499 A-to-I Human chr8 + 97848006 97848006 97848006 AAAGTACTGGCTGGGCATGGTGGCTCATGCCTATAATCCCTGTACTTTGGGAGGCTGAGGCAGTC AAAGTACTGGCTGGGCATGGTGGCTCATGCCTGTAATCCCTGTACTTTGGGAGGCTGAGGCAGTC A G LAPTM4B Ensembl:ENSG00000104341 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1446956192 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 51049 RMVar_ID_51049 Human_SNP_ID_374558197 A-to-I Human chr8 + 98031199 98031199 98031199 TCTCTGAAAAAAAATTTAACAATTAGCTAGGCATGATGGCACACACCTGTAGTCTCAGCTACTTG TCTCTGAAAAAAAATTTAACAATTAGCTAGGCCTGATGGCACACACCTGTAGTCTCAGCTACTTG A C MATN2 Ensembl:ENSG00000132561 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1191225481 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_253336 51050 RMVar_ID_51050 Human_SNP_ID_374561593 A-to-I Human chr8 - 98043265 98043265 98043265 AAAATTAGCTGGGTGTGGTGGTGCACGCCTGTAATCCCAGCTACTTGAGAGGCTGAGGCAGGAGA AAAATTAGCTGGGTGTGGTGGTGCACGCCTGTGATCCCAGCTACTTGAGAGGCTGAGGCAGGAGA T C RPL30 Ensembl:ENSG00000156482 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1301852209 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18991,RMVar_hsa_circ_127095,RMVar_hsa_circ_53918,RMVar_hsa_circ_253337 51051 RMVar_ID_51051 Human_SNP_ID_374561616 A-to-I Human chr8 - 98043353 98043353 98043353 GGGAGGCTGAGGCGGGCGGATCCCTTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGA GGGAGGCTGAGGCGGGCGGATCCCTTGAGGTCGGGAGTTCGAGACCAGCCTGGCCAACATGGTGA T C RPL30 Ensembl:ENSG00000156482 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1288753210 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18991,RMVar_hsa_circ_127095,RMVar_hsa_circ_53918,RMVar_hsa_circ_253337 51052 RMVar_ID_51052 Human_SNP_ID_374561629 A-to-I Human chr8 - 98043399 98043399 98043399 GAATAGGGCTGTGTGCCGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGCGG GAATAGGGCTGTGTGCCGTGGCTCACACCTGTGATCCCAGCACTTTGGGAGGCTGAGGCGGGCGG T C RPL30 Ensembl:ENSG00000156482 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1243207955 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18991,RMVar_hsa_circ_127095,RMVar_hsa_circ_53918,RMVar_hsa_circ_253337 51053 RMVar_ID_51053 Human_SNP_ID_374561631 A-to-I Human chr8 - 98043405 98043403 98043405 AAAAAAGAATAGGGCTGTGTGCCGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGC AAAAAAGAATAGGGCTGTGTGCCGTGGCTCAC__CTGTAATCCCAGCACTTTGGGAGGCTGAGGC GGT G RPL30 Ensembl:ENSG00000156482 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1320937423 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_18991,RMVar_hsa_circ_127095,RMVar_hsa_circ_53918,RMVar_hsa_circ_253337 51054 RMVar_ID_51054 Human_SNP_ID_374561632 A-to-I Human chr8 - 98043405 98043405 98043405 AAAAAAGAATAGGGCTGTGTGCCGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGC AAAAAAGAATAGGGCTGTGTGCCGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGC T C RPL30 Ensembl:ENSG00000156482 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1261718971 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18991,RMVar_hsa_circ_127095,RMVar_hsa_circ_53918,RMVar_hsa_circ_253337 51055 RMVar_ID_51055 Human_SNP_ID_374561795 A-to-I Human chr8 - 98043869 98043869 98043869 ACCTTAGGTGATCCACCCACCTCGGCCTCCCAAACTGCTGAGATTACAGGTGTGAGCTACCGTGC ACCTTAGGTGATCCACCCACCTCGGCCTCCCAGACTGCTGAGATTACAGGTGTGAGCTACCGTGC T C RPL30 Ensembl:ENSG00000156482 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs941247955 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18991,RMVar_hsa_circ_127095,RMVar_hsa_circ_53918,RMVar_hsa_circ_253337 51056 RMVar_ID_51056 Human_SNP_ID_374561848 A-to-I Human chr8 - 98044047 98044047 98044047 GGAGTGCAATGGCACAATCTAAGCTCACTGCAACCTCTGCCTCCCAGGTTCAAGCAATTCTGCCT GGAGTGCAATGGCACAATCTAAGCTCACTGCAGCCTCTGCCTCCCAGGTTCAAGCAATTCTGCCT T C RPL30 Ensembl:ENSG00000156482 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs958954525 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18991,RMVar_hsa_circ_127095,RMVar_hsa_circ_53918,RMVar_hsa_circ_253337 51057 RMVar_ID_51057 Human_SNP_ID_374561853 A-to-I Human chr8 - 98044071 98044071 98044071 AGTTTTGCTCTTGTCACCCCGGCTGGAGTGCAATGGCACAATCTAAGCTCACTGCAACCTCTGCC AGTTTTGCTCTTGTCACCCCGGCTGGAGTGCAGTGGCACAATCTAAGCTCACTGCAACCTCTGCC T C RPL30 Ensembl:ENSG00000156482 Protein coding intron GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 29129909,32596459 RNA-Seq:(High) rs1015369191 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16517326,Human_RBP_ID_22517462 RMVar_hsa_circ_18991,RMVar_hsa_circ_127095,RMVar_hsa_circ_53918,RMVar_hsa_circ_253337 51058 RMVar_ID_51058 Human_SNP_ID_374561861 A-to-I Human chr8 - 98044110 98044110 98044110 CCCGAGGTGCCATTTATTATTTTATTTTTTTTAAGACAGAGTTTTGCTCTTGTCACCCCGGCTGG CCCGAGGTGCCATTTATTATTTTATTTTTTTTGAGACAGAGTTTTGCTCTTGTCACCCCGGCTGG T C RPL30 Ensembl:ENSG00000156482 Protein coding intron GSE38233;GSE100210;GSE112787;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;293 Flip-In T-REx cells,empty vector;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,29967493,31158229,32596459 RNA-Seq:(High) rs975568758 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7869595,Human_RBP_ID_16501775,Human_RBP_ID_18124396 Human_Splice_Rec_995881 RMVar_hsa_circ_18991,RMVar_hsa_circ_127095,RMVar_hsa_circ_53918,RMVar_hsa_circ_253337 51059 RMVar_ID_51059 Human_SNP_ID_374578607 A-to-I Human chr8 - 98108982 98108982 98108982 TTGCCCAGGCTGATCTCAAACTCCTGGTCCCAAGCGATCCTCCTGCTTCACCCTCCCAAAGCACT TTGCCCAGGCTGATCTCAAACTCCTGGTCCCAGGCGATCCTCCTGCTTCACCCTCCCAAAGCACT T C RIDA Ensembl:ENSG00000132541 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1314827057 Functional Loss SNV dbSNP153 33..33 33 - - - 51060 RMVar_ID_51060 Human_SNP_ID_374604222 A-to-I Human chr8 - 98219031 98219031 98219031 CTCACTCCTACCCCTGATCCTGTTGGAAATGTAAAGTCTCTTGAACTTGACCCCCTTTTCACATT CTCACTCCTACCCCTGATCCTGTTGGAAATGTGAAGTCTCTTGAACTTGACCCCCTTTTCACATT T C NIPAL2 Ensembl:ENSG00000104361 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs890947145 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15809,RMVar_hsa_circ_102471,RMVar_hsa_circ_111987,RMVar_hsa_circ_109952,RMVar_hsa_circ_253351,RMVar_hsa_circ_253352,RMVar_hsa_circ_31123,RMVar_hsa_circ_44330,RMVar_hsa_circ_253353,RMVar_hsa_circ_253354,RMVar_hsa_circ_316942,RMVar_hsa_circ_357904,RMVar_hsa_circ_68551,RMVar_hsa_circ_253355 51061 RMVar_ID_51061 Human_SNP_ID_374604223 A-to-I Human chr8 - 98219031 98219031 98219031 CTCACTCCTACCCCTGATCCTGTTGGAAATGTAAAGTCTCTTGAACTTGACCCCCTTTTCACATT CTCACTCCTACCCCTGATCCTGTTGGAAATGTCAAGTCTCTTGAACTTGACCCCCTTTTCACATT T G NIPAL2 Ensembl:ENSG00000104361 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs890947145 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15809,RMVar_hsa_circ_102471,RMVar_hsa_circ_111987,RMVar_hsa_circ_109952,RMVar_hsa_circ_253351,RMVar_hsa_circ_253352,RMVar_hsa_circ_31123,RMVar_hsa_circ_44330,RMVar_hsa_circ_253353,RMVar_hsa_circ_253354,RMVar_hsa_circ_316942,RMVar_hsa_circ_357904,RMVar_hsa_circ_68551,RMVar_hsa_circ_253355 51062 RMVar_ID_51062 Human_SNP_ID_374617977 A-to-I Human chr8 - 98277195 98277195 98277195 AAATTAGATCGCGGTGATGGCTGCACAACTGTATGAGTATATTAAAAACTATTGAGTTGTACACT AAATTAGATCGCGGTGATGGCTGCACAACTGTGTGAGTATATTAAAAACTATTGAGTTGTACACT T C NIPAL2 Ensembl:ENSG00000104361 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs929653993 Functional Loss SNV dbSNP153 33..33 33 - - - 51063 RMVar_ID_51063 Human_SNP_ID_374749244 A-to-I Human chr8 - 98825624 98825624 98825624 CGAGTTCCCAGAGTTTCCCTCTGTGGTGCCCTAGGCTCGGCCGGCCGGTGCCCCGGCTCCTTTCC CGAGTTCCCAGAGTTTCCCTCTGTGGTGCCCTGGGCTCGGCCGGCCGGTGCCCCGGCTCCTTTCC T C STK3 Ensembl:ENSG00000104375 Protein coding 5'UTR GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) 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 51064 RMVar_ID_51064 Human_SNP_ID_374791791 A-to-I Human chr8 - 99006391 99006391 99006391 GGCCAGGTATGATGGTGTACACCTATACTCCCAGCTACTTGGGAGACTGAGGTGAGATGATCACT GGCCAGGTATGATGGTGTACACCTATACTCCCGGCTACTTGGGAGACTGAGGTGAGATGATCACT T C VPS13B-DT Ensembl:ENSG00000253948 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1437179982 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17578506,Human_RBP_ID_24237104 51065 RMVar_ID_51065 Human_SNP_ID_374795424 A-to-I Human chr8 + 99021785 99021785 99021785 AGTGCCAGTGCCACCATGCCCGAATAATTTTTATACTTTTTGTAGAGACGAGGTCTCACGATGTT AGTGCCAGTGCCACCATGCCCGAATAATTTTTTTACTTTTTGTAGAGACGAGGTCTCACGATGTT A T VPS13B Ensembl:ENSG00000132549 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1159749141 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54221,RMVar_hsa_circ_78807,RMVar_hsa_circ_304928,RMVar_hsa_circ_354426,RMVar_hsa_circ_253384,RMVar_hsa_circ_315173,RMVar_hsa_circ_86275,RMVar_hsa_circ_26622,RMVar_hsa_circ_48175,RMVar_hsa_circ_253385,RMVar_hsa_circ_4767 51066 RMVar_ID_51066 Human_SNP_ID_374807817 A-to-I Human chr8 + 99070044 99070044 99070044 CCCCCGCCACGGCATCCCAAGTAGCTAGGGCTATAGACATGCACCACCATGCCCAGCTGATTTTT CCCCCGCCACGGCATCCCAAGTAGCTAGGGCTGTAGACATGCACCACCATGCCCAGCTGATTTTT A G VPS13B Ensembl:ENSG00000132549 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1363130321 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17746,RMVar_hsa_circ_54221,RMVar_hsa_circ_78807,RMVar_hsa_circ_304928,RMVar_hsa_circ_354426,RMVar_hsa_circ_253384,RMVar_hsa_circ_86275,RMVar_hsa_circ_26622,RMVar_hsa_circ_48175,RMVar_hsa_circ_253385,RMVar_hsa_circ_4767,RMVar_hsa_circ_63277,RMVar_hsa_circ_369378,RMVar_hsa_circ_253386 51067 RMVar_ID_51067 Human_SNP_ID_374818930 A-to-I Human chr8 + 99115716 99115716 99115716 CTTTTTCAAAATGCAGATTCATACTTTAGTGGAAAGTTTGAAACTTTCTATCACAGATCAACAAC CTTTTTCAAAATGCAGATTCATACTTTAGTGGGAAGTTTGAAACTTTCTATCACAGATCAACAAC A G VPS13B Ensembl:ENSG00000132549 Protein coding CDS GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1170251206 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_27831455 Human_Splice_Rec_996348,Human_Splice_Rec_996382,Human_Splice_Rec_996448,Human_Splice_Rec_996570,Human_Splice_Rec_996692 RMVar_hsa_circ_5797,RMVar_hsa_circ_17746,RMVar_hsa_circ_54221,RMVar_hsa_circ_78807,RMVar_hsa_circ_304928,RMVar_hsa_circ_253384,RMVar_hsa_circ_86275,RMVar_hsa_circ_26622,RMVar_hsa_circ_48175,RMVar_hsa_circ_253385,RMVar_hsa_circ_4767,RMVar_hsa_circ_63277,RMVar_hsa_circ_369378,RMVar_hsa_circ_53044,RMVar_hsa_circ_281944,RMVar_hsa_circ_297151,RMVar_hsa_circ_309067,RMVar_hsa_circ_354605,RMVar_hsa_circ_253386,RMVar_hsa_circ_326013,RMVar_hsa_circ_118050,RMVar_hsa_circ_274167,RMVar_hsa_circ_63009,RMVar_hsa_circ_253389,RMVar_hsa_circ_253391,RMVar_hsa_circ_253392,RMVar_hsa_circ_253390,RMVar_hsa_circ_20726,RMVar_hsa_circ_55273,RMVar_hsa_circ_83817,RMVar_hsa_circ_303756,RMVar_hsa_circ_58295,RMVar_hsa_circ_74443,RMVar_hsa_circ_253393,RMVar_hsa_circ_253394,RMVar_hsa_circ_330959,RMVar_hsa_circ_363519,RMVar_hsa_circ_253395,RMVar_hsa_circ_82675,RMVar_hsa_circ_15741,RMVar_hsa_circ_253396,RMVar_hsa_circ_253397 51068 RMVar_ID_51068 Human_SNP_ID_374841450 A-to-I Human chr8 + 99211612 99211612 99211612 TAGAGCCTGTTACTACTGGAAACCCCGTTTCTACTAAAAATACAAAAATTAGCTGGACGTGGTGG TAGAGCCTGTTACTACTGGAAACCCCGTTTCTGCTAAAAATACAAAAATTAGCTGGACGTGGTGG A G VPS13B Ensembl:ENSG00000132549 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs533090650 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54221,RMVar_hsa_circ_304928,RMVar_hsa_circ_86275,RMVar_hsa_circ_253385,RMVar_hsa_circ_369378,RMVar_hsa_circ_253386,RMVar_hsa_circ_118050,RMVar_hsa_circ_274167,RMVar_hsa_circ_253392,RMVar_hsa_circ_83817,RMVar_hsa_circ_58295,RMVar_hsa_circ_253393,RMVar_hsa_circ_82675,RMVar_hsa_circ_21675,RMVar_hsa_circ_253397,RMVar_hsa_circ_99487,RMVar_hsa_circ_48366,RMVar_hsa_circ_253401,RMVar_hsa_circ_296740,RMVar_hsa_circ_76804,RMVar_hsa_circ_109274,RMVar_hsa_circ_93278,RMVar_hsa_circ_253406,RMVar_hsa_circ_253407,RMVar_hsa_circ_10226,RMVar_hsa_circ_253408,RMVar_hsa_circ_66533,RMVar_hsa_circ_64847,RMVar_hsa_circ_113841,RMVar_hsa_circ_112402,RMVar_hsa_circ_75473,RMVar_hsa_circ_253412,RMVar_hsa_circ_361201,RMVar_hsa_circ_301431,RMVar_hsa_circ_281947,RMVar_hsa_circ_120883,RMVar_hsa_circ_253417,RMVar_hsa_circ_66847,RMVar_hsa_circ_67430,RMVar_hsa_circ_55639,RMVar_hsa_circ_253415,RMVar_hsa_circ_253416,RMVar_hsa_circ_299019,RMVar_hsa_circ_369602,RMVar_hsa_circ_84609,RMVar_hsa_circ_253419,RMVar_hsa_circ_253420,RMVar_hsa_circ_253421 51069 RMVar_ID_51069 Human_SNP_ID_374841547 A-to-I Human chr8 + 99212010 99212010 99212010 TGCCTCCCGGGTTCATGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCGTCTG TGCCTCCCGGGTTCATGCGATTCTCCTGCCTCCGCCTCCTGAGTAGCTGGGATTACAGGCGTCTG A C VPS13B Ensembl:ENSG00000132549 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs900332191 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54221,RMVar_hsa_circ_304928,RMVar_hsa_circ_86275,RMVar_hsa_circ_253385,RMVar_hsa_circ_369378,RMVar_hsa_circ_253386,RMVar_hsa_circ_118050,RMVar_hsa_circ_274167,RMVar_hsa_circ_253392,RMVar_hsa_circ_83817,RMVar_hsa_circ_58295,RMVar_hsa_circ_253393,RMVar_hsa_circ_82675,RMVar_hsa_circ_21675,RMVar_hsa_circ_253397,RMVar_hsa_circ_99487,RMVar_hsa_circ_48366,RMVar_hsa_circ_253401,RMVar_hsa_circ_296740,RMVar_hsa_circ_76804,RMVar_hsa_circ_109274,RMVar_hsa_circ_93278,RMVar_hsa_circ_253406,RMVar_hsa_circ_253407,RMVar_hsa_circ_10226,RMVar_hsa_circ_253408,RMVar_hsa_circ_66533,RMVar_hsa_circ_64847,RMVar_hsa_circ_113841,RMVar_hsa_circ_112402,RMVar_hsa_circ_75473,RMVar_hsa_circ_253412,RMVar_hsa_circ_361201,RMVar_hsa_circ_301431,RMVar_hsa_circ_281947,RMVar_hsa_circ_120883,RMVar_hsa_circ_253417,RMVar_hsa_circ_66847,RMVar_hsa_circ_67430,RMVar_hsa_circ_55639,RMVar_hsa_circ_253415,RMVar_hsa_circ_253416,RMVar_hsa_circ_299019,RMVar_hsa_circ_369602,RMVar_hsa_circ_84609,RMVar_hsa_circ_253419,RMVar_hsa_circ_253420,RMVar_hsa_circ_253421 51070 RMVar_ID_51070 Human_SNP_ID_374897843 A-to-I Human chr8 + 99444744 99444744 99444744 GAGGCTGAAGTGCAGTGGTGCAATCACGGCTCACTGCCGCCTTGACCGCCGGAGCTCAATTGATC GAGGCTGAAGTGCAGTGGTGCAATCACGGCTCTCTGCCGCCTTGACCGCCGGAGCTCAATTGATC A T VPS13B Ensembl:ENSG00000132549 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1328273162 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_54221,RMVar_hsa_circ_86275,RMVar_hsa_circ_253385,RMVar_hsa_circ_118050,RMVar_hsa_circ_253392,RMVar_hsa_circ_99487,RMVar_hsa_circ_253401,RMVar_hsa_circ_76804,RMVar_hsa_circ_109274,RMVar_hsa_circ_253406,RMVar_hsa_circ_253408,RMVar_hsa_circ_113841,RMVar_hsa_circ_112402,RMVar_hsa_circ_75473,RMVar_hsa_circ_253412,RMVar_hsa_circ_66847,RMVar_hsa_circ_55639,RMVar_hsa_circ_253415,RMVar_hsa_circ_369602,RMVar_hsa_circ_84609,RMVar_hsa_circ_68111,RMVar_hsa_circ_70088,RMVar_hsa_circ_65190,RMVar_hsa_circ_253420,RMVar_hsa_circ_253421,RMVar_hsa_circ_358946,RMVar_hsa_circ_72322,RMVar_hsa_circ_73001,RMVar_hsa_circ_70718,RMVar_hsa_circ_342473,RMVar_hsa_circ_100691,RMVar_hsa_circ_363334,RMVar_hsa_circ_253424,RMVar_hsa_circ_356490,RMVar_hsa_circ_346619,RMVar_hsa_circ_75716,RMVar_hsa_circ_253429,RMVar_hsa_circ_253426,RMVar_hsa_circ_253425,RMVar_hsa_circ_376082,RMVar_hsa_circ_279722,RMVar_hsa_circ_301484,RMVar_hsa_circ_336009,RMVar_hsa_circ_350555,RMVar_hsa_circ_369574,RMVar_hsa_circ_350071,RMVar_hsa_circ_309738,RMVar_hsa_circ_298236,RMVar_hsa_circ_287727,RMVar_hsa_circ_103091,RMVar_hsa_circ_271087,RMVar_hsa_circ_75258,RMVar_hsa_circ_253431,RMVar_hsa_circ_253433,RMVar_hsa_circ_253435,RMVar_hsa_circ_253437,RMVar_hsa_circ_24038,RMVar_hsa_circ_253436,RMVar_hsa_circ_253434,RMVar_hsa_circ_253432,RMVar_hsa_circ_253438,RMVar_hsa_circ_83819,RMVar_hsa_circ_363124,RMVar_hsa_circ_371856,RMVar_hsa_circ_368697,RMVar_hsa_circ_307168,RMVar_hsa_circ_253440,RMVar_hsa_circ_68926,RMVar_hsa_circ_253439 51071 RMVar_ID_51071 Human_SNP_ID_374949977 A-to-I Human chr8 + 99662856 99662856 99662856 ATCACTTGAGACCAAGAATTCCACACCAGCCTAGCCAACATGGTGAAACCCTGTCTCTACTAAAA ATCACTTGAGACCAAGAATTCCACACCAGCCTGGCCAACATGGTGAAACCCTGTCTCTACTAAAA A G VPS13B Ensembl:ENSG00000132549 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1020016189 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86275,RMVar_hsa_circ_253385,RMVar_hsa_circ_99487,RMVar_hsa_circ_253401,RMVar_hsa_circ_113841,RMVar_hsa_circ_112402,RMVar_hsa_circ_253412,RMVar_hsa_circ_253415,RMVar_hsa_circ_84609,RMVar_hsa_circ_68111,RMVar_hsa_circ_70088,RMVar_hsa_circ_253421,RMVar_hsa_circ_72322,RMVar_hsa_circ_73001,RMVar_hsa_circ_75716,RMVar_hsa_circ_253425,RMVar_hsa_circ_350555,RMVar_hsa_circ_24038,RMVar_hsa_circ_68926,RMVar_hsa_circ_375971,RMVar_hsa_circ_98681,RMVar_hsa_circ_253446,RMVar_hsa_circ_253447,RMVar_hsa_circ_366825,RMVar_hsa_circ_49684,RMVar_hsa_circ_253463,RMVar_hsa_circ_46324,RMVar_hsa_circ_35806,RMVar_hsa_circ_125771,RMVar_hsa_circ_44694,RMVar_hsa_circ_369226,RMVar_hsa_circ_353765,RMVar_hsa_circ_103009,RMVar_hsa_circ_253462 51072 RMVar_ID_51072 Human_SNP_ID_375002905 A-to-I Human chr8 - 99885413 99885413 99885413 TTTTGATTACAGTAGTCCGTTTTATCTAAGATATGTTTCAAGACCCCTCTAGTGGATTCTTGAAA TTTTGATTACAGTAGTCCGTTTTATCTAAGATGTGTTTCAAGACCCCTCTAGTGGATTCTTGAAA T C COX6C Ensembl:ENSG00000164919 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1406713697 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61370,RMVar_hsa_circ_274598,RMVar_hsa_circ_253478 51073 RMVar_ID_51073 Human_SNP_ID_375004519 A-to-I Human chr8 - 99891333 99891333 99891333 TTGTTCAGGCTGGTCTTGAACTCCTGGGCTCAAGGGATTCACCTGCCTTGGCCTGCTAAAGTGCT TTGTTCAGGCTGGTCTTGAACTCCTGGGCTCAGGGGATTCACCTGCCTTGGCCTGCTAAAGTGCT T C COX6C Ensembl:ENSG00000164919 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1297374187 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_61370,RMVar_hsa_circ_315033 51074 RMVar_ID_51074 Human_SNP_ID_375083851 A-to-I Human chr8 + 100225600 100225600 100225600 CCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCATGTACCACCACACCTGGCTAATTTTAGT CCTGCCTCAGCCTCCTGAGTAGCTGGGATTACGGGCATGTACCACCACACCTGGCTAATTTTAGT A G SPAG1 Ensembl:ENSG00000104450 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1368898423 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_253490,RMVar_hsa_circ_8458,RMVar_hsa_circ_449,RMVar_hsa_circ_74794,RMVar_hsa_circ_70278,RMVar_hsa_circ_266114,RMVar_hsa_circ_377031,RMVar_hsa_circ_37279,RMVar_hsa_circ_253489,RMVar_hsa_circ_311074,RMVar_hsa_circ_314488,RMVar_hsa_circ_294700,RMVar_hsa_circ_253491,RMVar_hsa_circ_300907,RMVar_hsa_circ_306676,RMVar_hsa_circ_253494,RMVar_hsa_circ_304252,RMVar_hsa_circ_253496 51075 RMVar_ID_51075 Human_SNP_ID_375083871 A-to-I Human chr8 + 100225675 100225674 100225675 TTGTTTGTCTTTAGTAGAGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTCCTGACCT TTGTTTGTCTTTAGTAGAGACAGGGTTTCACC_TGTTGGCCAGGCTGGTCTCAAACTCCTGACCT CA C SPAG1 Ensembl:ENSG00000104450 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1439849874 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_253490,RMVar_hsa_circ_8458,RMVar_hsa_circ_449,RMVar_hsa_circ_74794,RMVar_hsa_circ_70278,RMVar_hsa_circ_266114,RMVar_hsa_circ_377031,RMVar_hsa_circ_37279,RMVar_hsa_circ_253489,RMVar_hsa_circ_311074,RMVar_hsa_circ_314488,RMVar_hsa_circ_294700,RMVar_hsa_circ_253491,RMVar_hsa_circ_300907,RMVar_hsa_circ_306676,RMVar_hsa_circ_253494,RMVar_hsa_circ_304252,RMVar_hsa_circ_253496 51076 RMVar_ID_51076 Human_SNP_ID_375083962 A-to-I Human chr8 + 100226028 100226028 100226028 TAGTTTTTTTTTTTTTTTTTTGGTGGAGTCTCACTTTGATGTCCAGGCTAGAGTGCAGTGGTGTG TAGTTTTTTTTTTTTTTTTTTGGTGGAGTCTCGCTTTGATGTCCAGGCTAGAGTGCAGTGGTGTG A G SPAG1 Ensembl:ENSG00000104450 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1237655843 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_253490,RMVar_hsa_circ_8458,RMVar_hsa_circ_449,RMVar_hsa_circ_74794,RMVar_hsa_circ_70278,RMVar_hsa_circ_266114,RMVar_hsa_circ_377031,RMVar_hsa_circ_37279,RMVar_hsa_circ_253489,RMVar_hsa_circ_311074,RMVar_hsa_circ_314488,RMVar_hsa_circ_294700,RMVar_hsa_circ_253491,RMVar_hsa_circ_300907,RMVar_hsa_circ_306676,RMVar_hsa_circ_253494,RMVar_hsa_circ_304252,RMVar_hsa_circ_253496 51077 RMVar_ID_51077 Human_SNP_ID_375083990 A-to-I Human chr8 + 100226177 100226177 100226177 TGCCACCACGCACGGCTAATTTTTGTATTTTTAGTAGAGACGGAGTCTCCCTATGTTGCCCATGC TGCCACCACGCACGGCTAATTTTTGTATTTTTGGTAGAGACGGAGTCTCCCTATGTTGCCCATGC A G SPAG1 Ensembl:ENSG00000104450 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs142774808 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_253490,RMVar_hsa_circ_8458,RMVar_hsa_circ_449,RMVar_hsa_circ_74794,RMVar_hsa_circ_70278,RMVar_hsa_circ_266114,RMVar_hsa_circ_377031,RMVar_hsa_circ_37279,RMVar_hsa_circ_253489,RMVar_hsa_circ_311074,RMVar_hsa_circ_314488,RMVar_hsa_circ_294700,RMVar_hsa_circ_253491,RMVar_hsa_circ_300907,RMVar_hsa_circ_306676,RMVar_hsa_circ_253494,RMVar_hsa_circ_304252,RMVar_hsa_circ_253496 51078 RMVar_ID_51078 Human_SNP_ID_375084069 A-to-I Human chr8 + 100226627 100226627 100226627 TTGGGAGGCTGAGGTGGGAGGATCCCGAGCCCAGGAAGGTTGAGGCTGCAGTGAGCTGTGATGGT TTGGGAGGCTGAGGTGGGAGGATCCCGAGCCCGGGAAGGTTGAGGCTGCAGTGAGCTGTGATGGT A G SPAG1 Ensembl:ENSG00000104450 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1452608945 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_253490,RMVar_hsa_circ_8458,RMVar_hsa_circ_449,RMVar_hsa_circ_74794,RMVar_hsa_circ_70278,RMVar_hsa_circ_266114,RMVar_hsa_circ_377031,RMVar_hsa_circ_37279,RMVar_hsa_circ_253489,RMVar_hsa_circ_311074,RMVar_hsa_circ_314488,RMVar_hsa_circ_294700,RMVar_hsa_circ_253491,RMVar_hsa_circ_300907,RMVar_hsa_circ_306676,RMVar_hsa_circ_253494,RMVar_hsa_circ_304252,RMVar_hsa_circ_253496 51079 RMVar_ID_51079 Human_SNP_ID_375084491 A-to-I Human chr8 + 100228566 100228566 100228566 AAAACCCTGTCTCTACTAAAAATACAAAAATTAGCTGAGCATGGTAGCATGCCCCTGTAGTCCCA AAAACCCTGTCTCTACTAAAAATACAAAAATTGGCTGAGCATGGTAGCATGCCCCTGTAGTCCCA A G SPAG1 Ensembl:ENSG00000104450 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs568091920 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_253490,RMVar_hsa_circ_8458,RMVar_hsa_circ_449,RMVar_hsa_circ_74794,RMVar_hsa_circ_70278,RMVar_hsa_circ_266114,RMVar_hsa_circ_377031,RMVar_hsa_circ_37279,RMVar_hsa_circ_253489,RMVar_hsa_circ_311074,RMVar_hsa_circ_314488,RMVar_hsa_circ_294700,RMVar_hsa_circ_253491,RMVar_hsa_circ_300907,RMVar_hsa_circ_306676,RMVar_hsa_circ_253494,RMVar_hsa_circ_304252,RMVar_hsa_circ_253496 51080 RMVar_ID_51080 Human_SNP_ID_375084495 A-to-I Human chr8 + 100228579 100228579 100228579 TACTAAAAATACAAAAATTAGCTGAGCATGGTAGCATGCCCCTGTAGTCCCAGCTGCTTGGGAGG TACTAAAAATACAAAAATTAGCTGAGCATGGTGGCATGCCCCTGTAGTCCCAGCTGCTTGGGAGG A G SPAG1 Ensembl:ENSG00000104450 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1487346044 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_253490,RMVar_hsa_circ_8458,RMVar_hsa_circ_449,RMVar_hsa_circ_74794,RMVar_hsa_circ_70278,RMVar_hsa_circ_266114,RMVar_hsa_circ_377031,RMVar_hsa_circ_37279,RMVar_hsa_circ_253489,RMVar_hsa_circ_311074,RMVar_hsa_circ_314488,RMVar_hsa_circ_294700,RMVar_hsa_circ_253491,RMVar_hsa_circ_300907,RMVar_hsa_circ_306676,RMVar_hsa_circ_253494,RMVar_hsa_circ_304252,RMVar_hsa_circ_253496 51081 RMVar_ID_51081 Human_SNP_ID_375084639 A-to-I Human chr8 + 100229297 100229297 100229297 CAAAAATTAGCCGGGCGTGGTGGTGGGTGCCTATAGTCCCAGCTACATGGGAGGCTGAGGCAGGA CAAAAATTAGCCGGGCGTGGTGGTGGGTGCCTGTAGTCCCAGCTACATGGGAGGCTGAGGCAGGA A G SPAG1 Ensembl:ENSG00000104450 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1432904736 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_253490,RMVar_hsa_circ_8458,RMVar_hsa_circ_449,RMVar_hsa_circ_74794,RMVar_hsa_circ_70278,RMVar_hsa_circ_266114,RMVar_hsa_circ_377031,RMVar_hsa_circ_37279,RMVar_hsa_circ_253489,RMVar_hsa_circ_311074,RMVar_hsa_circ_314488,RMVar_hsa_circ_294700,RMVar_hsa_circ_253491,RMVar_hsa_circ_300907,RMVar_hsa_circ_306676,RMVar_hsa_circ_253494,RMVar_hsa_circ_304252,RMVar_hsa_circ_253496 51082 RMVar_ID_51082 Human_SNP_ID_375084643 A-to-I Human chr8 + 100229309 100229309 100229309 GGGCGTGGTGGTGGGTGCCTATAGTCCCAGCTACATGGGAGGCTGAGGCAGGAGAATGGCGTGAA GGGCGTGGTGGTGGGTGCCTATAGTCCCAGCTGCATGGGAGGCTGAGGCAGGAGAATGGCGTGAA A G SPAG1 Ensembl:ENSG00000104450 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1160306738 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_253490,RMVar_hsa_circ_8458,RMVar_hsa_circ_449,RMVar_hsa_circ_74794,RMVar_hsa_circ_70278,RMVar_hsa_circ_266114,RMVar_hsa_circ_377031,RMVar_hsa_circ_37279,RMVar_hsa_circ_253489,RMVar_hsa_circ_311074,RMVar_hsa_circ_314488,RMVar_hsa_circ_294700,RMVar_hsa_circ_253491,RMVar_hsa_circ_300907,RMVar_hsa_circ_306676,RMVar_hsa_circ_253494,RMVar_hsa_circ_304252,RMVar_hsa_circ_253496 51083 RMVar_ID_51083 Human_SNP_ID_375101242 A-to-I Human chr8 - 100299082 100299082 100299082 TTCCCTTCTGTTGAGAACCAAGGGACACAGTAAGCAAAATGTGTCTGTTTTCCTTTGGATATGCA TTCCCTTCTGTTGAGAACCAAGGGACACAGTAGGCAAAATGTGTCTGTTTTCCTTTGGATATGCA T C RNF19A Ensembl:ENSG00000034677 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs541114835 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86440,RMVar_hsa_circ_253507,RMVar_hsa_circ_27822 51084 RMVar_ID_51084 Human_SNP_ID_375102287 A-to-I Human chr8 - 100303719 100303719 100303719 AGGTTTTGCCATGTTGGCCAGGCTGATTTCGAACTCCTGGACTCAAGTGATCCGCCCACGTCAGC AGGTTTTGCCATGTTGGCCAGGCTGATTTCGAGCTCCTGGACTCAAGTGATCCGCCCACGTCAGC T C RNF19A Ensembl:ENSG00000034677 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1473407523 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16297828 51085 RMVar_ID_51085 Human_SNP_ID_375102403 A-to-I Human chr8 - 100304053 100304053 100304053 ACTTGGGAGGCTGAGGCAGGAGAATTGCTCCAACCTGAGAGGTGGAGGTTATAGTGAGCCGAGAT ACTTGGGAGGCTGAGGCAGGAGAATTGCTCCAGCCTGAGAGGTGGAGGTTATAGTGAGCCGAGAT T C RNF19A Ensembl:ENSG00000034677 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1272327320 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17578690 51086 RMVar_ID_51086 Human_SNP_ID_375102404 A-to-I Human chr8 - 100304053 100304053 100304053 ACTTGGGAGGCTGAGGCAGGAGAATTGCTCCAACCTGAGAGGTGGAGGTTATAGTGAGCCGAGAT ACTTGGGAGGCTGAGGCAGGAGAATTGCTCCACCCTGAGAGGTGGAGGTTATAGTGAGCCGAGAT T G RNF19A Ensembl:ENSG00000034677 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1272327320 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17578690 51087 RMVar_ID_51087 Human_SNP_ID_375138989 A-to-I Human chr8 + 100456765 100456765 100456765 GAGCTCAGGCAATCTACCTGCCTAAGCCTTGCAAAATGCTAGGATTACAGGAAGTTGTTTTCGTT GAGCTCAGGCAATCTACCTGCCTAAGCCTTGCGAAATGCTAGGATTACAGGAAGTTGTTTTCGTT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs938464954 Functional Loss SNV dbSNP153 33..33 33 - - - 51088 RMVar_ID_51088 Human_SNP_ID_375156250 A-to-I Human chr8 - 100530480 100530480 100530480 ACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAACTCGGGAGATGGAGGTTGCAGTGAGCCAAGAC ACTTGGGAGGCTGAGGCAGGAGAATCGCTTGACCTCGGGAGATGGAGGTTGCAGTGAGCCAAGAC T G ANKRD46 Ensembl:ENSG00000186106 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1324419959 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_313800,RMVar_hsa_circ_253519,RMVar_hsa_circ_253517,RMVar_hsa_circ_311223 51089 RMVar_ID_51089 Human_SNP_ID_375156253 A-to-I Human chr8 - 100530495 100530495 100530495 CCTGTAATTCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAACTCGGGAGATGGAGGTT CCTGTAATTCCAGCTACTTGGGAGGCTGAGGCGGGAGAATCGCTTGAACTCGGGAGATGGAGGTT T C ANKRD46 Ensembl:ENSG00000186106 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs754220579 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_313800,RMVar_hsa_circ_253519,RMVar_hsa_circ_253517,RMVar_hsa_circ_311223 51090 RMVar_ID_51090 Human_SNP_ID_375161787 A-to-I Human chr8 - 100556293 100556293 100556293 GGGTGGGCTGGGCGAAGTGGCTCATGCCTGTAATCCCAACACTTTGGGAGGCCGAGACTGGAGGA GGGTGGGCTGGGCGAAGTGGCTCATGCCTGTATTCCCAACACTTTGGGAGGCCGAGACTGGAGGA T A ANKRD46 Ensembl:ENSG00000186106 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1310205513 Functional Loss SNV dbSNP153 33..33 33 - - - 51091 RMVar_ID_51091 Human_SNP_ID_375161790 A-to-I Human chr8 - 100556310 100556310 100556310 AGCCCATAAAAATGCTTGGGTGGGCTGGGCGAAGTGGCTCATGCCTGTAATCCCAACACTTTGGG AGCCCATAAAAATGCTTGGGTGGGCTGGGCGAGGTGGCTCATGCCTGTAATCCCAACACTTTGGG T C ANKRD46 Ensembl:ENSG00000186106 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1220064620 Functional Loss SNV dbSNP153 33..33 33 - - - 51092 RMVar_ID_51092 Human_SNP_ID_375199719 A-to-I Human chr8 - 100708326 100708326 100708326 TCAGCCTCCCAAGTAGCTGGGACTACAGGCACACGCCACCACGCCCAGCTAATTTTTTAAATTTT TCAGCCTCCCAAGTAGCTGGGACTACAGGCACCCGCCACCACGCCCAGCTAATTTTTTAAATTTT T G PABPC1 Ensembl:ENSG00000070756 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1292261471 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_10935,RMVar_hsa_circ_17325,RMVar_hsa_circ_310376,RMVar_hsa_circ_373272,RMVar_hsa_circ_345555,RMVar_hsa_circ_313470,RMVar_hsa_circ_306988,RMVar_hsa_circ_60384,RMVar_hsa_circ_98534,RMVar_hsa_circ_38716,RMVar_hsa_circ_253525,RMVar_hsa_circ_253527,RMVar_hsa_circ_253528,RMVar_hsa_circ_253526,RMVar_hsa_circ_253524,RMVar_hsa_circ_87543,RMVar_hsa_circ_48040,RMVar_hsa_circ_54383,RMVar_hsa_circ_19130,RMVar_hsa_circ_27644,RMVar_hsa_circ_343640,RMVar_hsa_circ_366004,RMVar_hsa_circ_376185,RMVar_hsa_circ_93010,RMVar_hsa_circ_253538,RMVar_hsa_circ_253542,RMVar_hsa_circ_53814,RMVar_hsa_circ_77140,RMVar_hsa_circ_253540,RMVar_hsa_circ_253541,RMVar_hsa_circ_253539,RMVar_hsa_circ_86470,RMVar_hsa_circ_107497,RMVar_hsa_circ_253546,RMVar_hsa_circ_253547 51093 RMVar_ID_51093 Human_SNP_ID_375201696 A-to-I Human chr8 - 100714539 100714539 100714539 TTTATTAGAGACGGGGTTTCACCGTGATGGCCAGGCTGGTCTCCAACTCCTGACCTCAAGTGATC TTTATTAGAGACGGGGTTTCACCGTGATGGCCGGGCTGGTCTCCAACTCCTGACCTCAAGTGATC T C PABPC1 Ensembl:ENSG00000070756 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355416896 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16299918 RMVar_hsa_circ_310376,RMVar_hsa_circ_345555,RMVar_hsa_circ_306988,RMVar_hsa_circ_98534,RMVar_hsa_circ_38716,RMVar_hsa_circ_253525,RMVar_hsa_circ_253526,RMVar_hsa_circ_253524,RMVar_hsa_circ_54383,RMVar_hsa_circ_19130,RMVar_hsa_circ_343640,RMVar_hsa_circ_93010,RMVar_hsa_circ_253538,RMVar_hsa_circ_53814,RMVar_hsa_circ_77140,RMVar_hsa_circ_253540,RMVar_hsa_circ_253539,RMVar_hsa_circ_107497,RMVar_hsa_circ_253548,RMVar_hsa_circ_78073,RMVar_hsa_circ_114306,RMVar_hsa_circ_253547,RMVar_hsa_circ_377715,RMVar_hsa_circ_291384,RMVar_hsa_circ_97314,RMVar_hsa_circ_253550,RMVar_hsa_circ_253551,RMVar_hsa_circ_253549,RMVar_hsa_circ_12771,RMVar_hsa_circ_355186,RMVar_hsa_circ_367461,RMVar_hsa_circ_311112,RMVar_hsa_circ_355315,RMVar_hsa_circ_253557,RMVar_hsa_circ_293230,RMVar_hsa_circ_38262,RMVar_hsa_circ_355499 51094 RMVar_ID_51094 Human_SNP_ID_375201720 A-to-I Human chr8 - 100714634 100714634 100714634 GCCTCCGCCTCCCGGGTTCAAGCAGTTCTCCTATCTCTACCTTGAGTAGCTGGGATTACAGGTGT GCCTCCGCCTCCCGGGTTCAAGCAGTTCTCCTGTCTCTACCTTGAGTAGCTGGGATTACAGGTGT T C PABPC1 Ensembl:ENSG00000070756 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs905176507 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16299921 RMVar_hsa_circ_310376,RMVar_hsa_circ_345555,RMVar_hsa_circ_306988,RMVar_hsa_circ_98534,RMVar_hsa_circ_38716,RMVar_hsa_circ_253525,RMVar_hsa_circ_253526,RMVar_hsa_circ_253524,RMVar_hsa_circ_54383,RMVar_hsa_circ_19130,RMVar_hsa_circ_343640,RMVar_hsa_circ_93010,RMVar_hsa_circ_253538,RMVar_hsa_circ_53814,RMVar_hsa_circ_77140,RMVar_hsa_circ_253540,RMVar_hsa_circ_253539,RMVar_hsa_circ_107497,RMVar_hsa_circ_253548,RMVar_hsa_circ_78073,RMVar_hsa_circ_114306,RMVar_hsa_circ_253547,RMVar_hsa_circ_377715,RMVar_hsa_circ_291384,RMVar_hsa_circ_97314,RMVar_hsa_circ_253550,RMVar_hsa_circ_253551,RMVar_hsa_circ_253549,RMVar_hsa_circ_12771,RMVar_hsa_circ_355186,RMVar_hsa_circ_367461,RMVar_hsa_circ_311112,RMVar_hsa_circ_355315,RMVar_hsa_circ_253557,RMVar_hsa_circ_293230,RMVar_hsa_circ_38262,RMVar_hsa_circ_355499 51095 RMVar_ID_51095 Human_SNP_ID_375202278 A-to-I Human chr8 - 100716256 100716256 100716256 GGTGGGATTACAGGTGTACACCACCACACCCAACTAATTTTTGTACTTTAGTAGAGACAGTTTCA GGTGGGATTACAGGTGTACACCACCACACCCAGCTAATTTTTGTACTTTAGTAGAGACAGTTTCA T C PABPC1 Ensembl:ENSG00000070756 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs999814972 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16300005 RMVar_hsa_circ_310376,RMVar_hsa_circ_306988,RMVar_hsa_circ_98534,RMVar_hsa_circ_38716,RMVar_hsa_circ_253525,RMVar_hsa_circ_253526,RMVar_hsa_circ_253524,RMVar_hsa_circ_54383,RMVar_hsa_circ_19130,RMVar_hsa_circ_343640,RMVar_hsa_circ_93010,RMVar_hsa_circ_253538,RMVar_hsa_circ_77140,RMVar_hsa_circ_253540,RMVar_hsa_circ_253539,RMVar_hsa_circ_107497,RMVar_hsa_circ_253548,RMVar_hsa_circ_78073,RMVar_hsa_circ_114306,RMVar_hsa_circ_253547,RMVar_hsa_circ_291384,RMVar_hsa_circ_97314,RMVar_hsa_circ_253550,RMVar_hsa_circ_253551,RMVar_hsa_circ_253549,RMVar_hsa_circ_12771,RMVar_hsa_circ_355186,RMVar_hsa_circ_367461,RMVar_hsa_circ_311112,RMVar_hsa_circ_253557,RMVar_hsa_circ_293230,RMVar_hsa_circ_38262,RMVar_hsa_circ_253558,RMVar_hsa_circ_336247,RMVar_hsa_circ_355499,RMVar_hsa_circ_314145 51096 RMVar_ID_51096 Human_SNP_ID_375202285 A-to-I Human chr8 - 100716279 100716279 100716279 GTCGTGCTTCAGCCTCCCAAGTAGGTGGGATTACAGGTGTACACCACCACACCCAACTAATTTTT GTCGTGCTTCAGCCTCCCAAGTAGGTGGGATTGCAGGTGTACACCACCACACCCAACTAATTTTT T C PABPC1 Ensembl:ENSG00000070756 Protein coding intron GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs995849712 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_310376,RMVar_hsa_circ_306988,RMVar_hsa_circ_98534,RMVar_hsa_circ_38716,RMVar_hsa_circ_253525,RMVar_hsa_circ_253526,RMVar_hsa_circ_253524,RMVar_hsa_circ_54383,RMVar_hsa_circ_19130,RMVar_hsa_circ_343640,RMVar_hsa_circ_93010,RMVar_hsa_circ_253538,RMVar_hsa_circ_77140,RMVar_hsa_circ_253540,RMVar_hsa_circ_253539,RMVar_hsa_circ_107497,RMVar_hsa_circ_253548,RMVar_hsa_circ_78073,RMVar_hsa_circ_114306,RMVar_hsa_circ_253547,RMVar_hsa_circ_291384,RMVar_hsa_circ_97314,RMVar_hsa_circ_253550,RMVar_hsa_circ_253551,RMVar_hsa_circ_253549,RMVar_hsa_circ_12771,RMVar_hsa_circ_355186,RMVar_hsa_circ_367461,RMVar_hsa_circ_311112,RMVar_hsa_circ_253557,RMVar_hsa_circ_293230,RMVar_hsa_circ_38262,RMVar_hsa_circ_253558,RMVar_hsa_circ_336247,RMVar_hsa_circ_355499,RMVar_hsa_circ_314145 51097 RMVar_ID_51097 Human_SNP_ID_375202294 A-to-I Human chr8 - 100716315 100716298 100716315 CTCACTGCCACCTCTGCCTCCCGGGTTCTAGCAATTGTCGTGCTTCAGCCTCCCAAGTAGGTGGG CTCACTGCCACCTCTGCCTCCCGGGTTCTAGC_________________CTCCCAAGTAGGTGGG GGCTGAAGCACGACAATT G PABPC1 Ensembl:ENSG00000070756 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1278620484 Functional Loss DEL dbSNP153 33..49 33 - - - Human_RBP_ID_8676389,Human_RBP_ID_16300006 RMVar_hsa_circ_310376,RMVar_hsa_circ_306988,RMVar_hsa_circ_98534,RMVar_hsa_circ_38716,RMVar_hsa_circ_253525,RMVar_hsa_circ_253526,RMVar_hsa_circ_253524,RMVar_hsa_circ_54383,RMVar_hsa_circ_19130,RMVar_hsa_circ_343640,RMVar_hsa_circ_93010,RMVar_hsa_circ_253538,RMVar_hsa_circ_77140,RMVar_hsa_circ_253540,RMVar_hsa_circ_253539,RMVar_hsa_circ_107497,RMVar_hsa_circ_253548,RMVar_hsa_circ_78073,RMVar_hsa_circ_114306,RMVar_hsa_circ_253547,RMVar_hsa_circ_291384,RMVar_hsa_circ_97314,RMVar_hsa_circ_253550,RMVar_hsa_circ_253551,RMVar_hsa_circ_253549,RMVar_hsa_circ_12771,RMVar_hsa_circ_355186,RMVar_hsa_circ_367461,RMVar_hsa_circ_311112,RMVar_hsa_circ_253557,RMVar_hsa_circ_293230,RMVar_hsa_circ_38262,RMVar_hsa_circ_253558,RMVar_hsa_circ_336247,RMVar_hsa_circ_355499,RMVar_hsa_circ_314145 51098 RMVar_ID_51098 Human_SNP_ID_375202294 A-to-I Human chr8 - 100716314 100716298 100716315 TCACTGCCACCTCTGCCTCCCGGGTTCTAGCAATTGTCGTGCTTCAGCCTCCCAAGTAGGTGGGA TCACTGCCACCTCTGCCTCCCGGGTTCTAGC_________________CTCCCAAGTAGGTGGGA GGCTGAAGCACGACAATT G PABPC1 Ensembl:ENSG00000070756 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1278620484 Functional Loss DEL dbSNP153 32..48 33 - - - Human_RBP_ID_8676389,Human_RBP_ID_16300006,Human_RBP_ID_26141133 RMVar_hsa_circ_310376,RMVar_hsa_circ_306988,RMVar_hsa_circ_98534,RMVar_hsa_circ_38716,RMVar_hsa_circ_253525,RMVar_hsa_circ_253526,RMVar_hsa_circ_253524,RMVar_hsa_circ_54383,RMVar_hsa_circ_19130,RMVar_hsa_circ_343640,RMVar_hsa_circ_93010,RMVar_hsa_circ_253538,RMVar_hsa_circ_77140,RMVar_hsa_circ_253540,RMVar_hsa_circ_253539,RMVar_hsa_circ_107497,RMVar_hsa_circ_253548,RMVar_hsa_circ_78073,RMVar_hsa_circ_114306,RMVar_hsa_circ_253547,RMVar_hsa_circ_291384,RMVar_hsa_circ_97314,RMVar_hsa_circ_253550,RMVar_hsa_circ_253551,RMVar_hsa_circ_253549,RMVar_hsa_circ_12771,RMVar_hsa_circ_355186,RMVar_hsa_circ_367461,RMVar_hsa_circ_311112,RMVar_hsa_circ_253557,RMVar_hsa_circ_293230,RMVar_hsa_circ_38262,RMVar_hsa_circ_253558,RMVar_hsa_circ_336247,RMVar_hsa_circ_355499,RMVar_hsa_circ_314145 51099 RMVar_ID_51099 Human_SNP_ID_375202313 A-to-I Human chr8 - 100716352 100716352 100716352 CTCTCTTGCCCAGGCTGGAGTGCAGTGGTGCAATCTACTCACTGCCACCTCTGCCTCCCGGGTTC CTCTCTTGCCCAGGCTGGAGTGCAGTGGTGCAGTCTACTCACTGCCACCTCTGCCTCCCGGGTTC T C PABPC1 Ensembl:ENSG00000070756 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs976801264 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5514026,Human_RBP_ID_16300007,Human_RBP_ID_26141135 RMVar_hsa_circ_310376,RMVar_hsa_circ_306988,RMVar_hsa_circ_98534,RMVar_hsa_circ_38716,RMVar_hsa_circ_253525,RMVar_hsa_circ_253526,RMVar_hsa_circ_253524,RMVar_hsa_circ_54383,RMVar_hsa_circ_19130,RMVar_hsa_circ_343640,RMVar_hsa_circ_93010,RMVar_hsa_circ_253538,RMVar_hsa_circ_77140,RMVar_hsa_circ_253540,RMVar_hsa_circ_253539,RMVar_hsa_circ_107497,RMVar_hsa_circ_253548,RMVar_hsa_circ_78073,RMVar_hsa_circ_114306,RMVar_hsa_circ_253547,RMVar_hsa_circ_291384,RMVar_hsa_circ_97314,RMVar_hsa_circ_253550,RMVar_hsa_circ_253551,RMVar_hsa_circ_253549,RMVar_hsa_circ_12771,RMVar_hsa_circ_355186,RMVar_hsa_circ_367461,RMVar_hsa_circ_311112,RMVar_hsa_circ_253557,RMVar_hsa_circ_293230,RMVar_hsa_circ_38262,RMVar_hsa_circ_253558,RMVar_hsa_circ_336247,RMVar_hsa_circ_355499,RMVar_hsa_circ_314145 51100 RMVar_ID_51100 Human_SNP_ID_375255883 A-to-I Human chr8 - 100927293 100927293 100927293 TCAAACTCCTGGACTCAAGAAGTGATCCTCCCACCTCAGCCTCCCAAAGTGTTGGGATTACAGGA TCAAACTCCTGGACTCAAGAAGTGATCCTCCCTCCTCAGCCTCCCAAAGTGTTGGGATTACAGGA T A YWHAZ Ensembl:ENSG00000164924 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1225818312 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126272,RMVar_hsa_circ_253562,RMVar_hsa_circ_253564,RMVar_hsa_circ_372883 51101 RMVar_ID_51101 Human_SNP_ID_375256133 A-to-I Human chr8 - 100928266 100928262 100928266 TTCTCAACTCTTTTTTTTTGAGACGGAGTCTCACTCTGTTGCCCAGGCTGGAGTGCAGTGGCACT TTCTCAACTCTTTTTTTTTGAGACGGAGTCTC____TGTTGCCCAGGCTGGAGTGCAGTGGCACT AGAGT A YWHAZ Ensembl:ENSG00000164924 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1433874731 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_126272,RMVar_hsa_circ_253562,RMVar_hsa_circ_253564,RMVar_hsa_circ_372883 51102 RMVar_ID_51102 Human_SNP_ID_375256135 A-to-I Human chr8 - 100928266 100928266 100928266 TTCTCAACTCTTTTTTTTTGAGACGGAGTCTCACTCTGTTGCCCAGGCTGGAGTGCAGTGGCACT TTCTCAACTCTTTTTTTTTGAGACGGAGTCTCGCTCTGTTGCCCAGGCTGGAGTGCAGTGGCACT T C YWHAZ Ensembl:ENSG00000164924 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1268151701 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126272,RMVar_hsa_circ_253562,RMVar_hsa_circ_253564,RMVar_hsa_circ_372883 51103 RMVar_ID_51103 Human_SNP_ID_375256676 A-to-I Human chr8 - 100930227 100930227 100930227 GGGTGTGATGGCATGTGCCTGCAGTCCCGGCTACTCGGGAGACTGAGGCAGAAGAATCACTTGAA GGGTGTGATGGCATGTGCCTGCAGTCCCGGCTGCTCGGGAGACTGAGGCAGAAGAATCACTTGAA T C YWHAZ Ensembl:ENSG00000164924 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs918451830 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26141298 RMVar_hsa_circ_126272,RMVar_hsa_circ_253562,RMVar_hsa_circ_253564,RMVar_hsa_circ_372883 51104 RMVar_ID_51104 Human_SNP_ID_375256719 A-to-I Human chr8 - 100930376 100930376 100930376 ACAGTTGGAGTTGGCTGGGCGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGC ACAGTTGGAGTTGGCTGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGC T C YWHAZ Ensembl:ENSG00000164924 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs536837987 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_126272,RMVar_hsa_circ_253562,RMVar_hsa_circ_253564,RMVar_hsa_circ_372883 51105 RMVar_ID_51105 Human_SNP_ID_375320427 A-to-I Human chr8 - 101182710 101182710 101182710 AATGTTTGGGCCAGTCACGGTGGCTCACGCCTACAATCCCAGCGCTTTGGGAGGCCAAGGCCAGC AATGTTTGGGCCAGTCACGGTGGCTCACGCCTGCAATCCCAGCGCTTTGGGAGGCCAAGGCCAGC T C ZNF706 Ensembl:ENSG00000120963 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1443767309 Functional Loss SNV dbSNP153 33..33 33 - - - 51106 RMVar_ID_51106 Human_SNP_ID_375572715 A-to-I Human chr8 - 102229647 102229647 102229647 CCAGGTAGCAGAGGCTGCAGTGAGCCCAGATCATGCCACTGTATTCCAGCCTGGGCAACAGAGTG CCAGGTAGCAGAGGCTGCAGTGAGCCCAGATCCTGCCACTGTATTCCAGCCTGGGCAACAGAGTG T G RRM2B Ensembl:ENSG00000048392 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277898911 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2470,RMVar_hsa_circ_286228,RMVar_hsa_circ_253579,RMVar_hsa_circ_253582,RMVar_hsa_circ_353037 51107 RMVar_ID_51107 Human_SNP_ID_375573750 A-to-I Human chr8 - 102233996 102233996 102233996 GCAACATAGCATGACCCCCATCTCTACAAAAAATTTAAAAATTATCCAGGTGTGGTGACGTGTGC GCAACATAGCATGACCCCCATCTCTACAAAAAGTTTAAAAATTATCCAGGTGTGGTGACGTGTGC T C RRM2B Ensembl:ENSG00000048392 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs975387091 Functional Loss SNV dbSNP153 33..33 33 - - - 51108 RMVar_ID_51108 Human_SNP_ID_375575601 A-to-I Human chr8 + 102241019 102241019 102241019 CAAAAATTAGCCGGGCGTGTTGGCGCATGCCTATAATTCTAGCTACTTGAGAGGCTGAGGCAGGA CAAAAATTAGCCGGGCGTGTTGGCGCATGCCTGTAATTCTAGCTACTTGAGAGGCTGAGGCAGGA A G UBR5-AS1 Ensembl:ENSG00000246263 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs959266282 Functional Loss SNV dbSNP153 33..33 33 - - - 51109 RMVar_ID_51109 Human_SNP_ID_375584344 A-to-I Human chr8 - 102277568 102277568 102277568 CAAGACCATACTGGCCAACATAGCCAAACCCCATCTCTACTAAAATTACAAAAAATTAGCTGGAC CAAGACCATACTGGCCAACATAGCCAAACCCCGTCTCTACTAAAATTACAAAAAATTAGCTGGAC T C UBR5 Ensembl:ENSG00000104517 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs936582754 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_288,RMVar_hsa_circ_86455,RMVar_hsa_circ_109109,RMVar_hsa_circ_253587,RMVar_hsa_circ_253588,RMVar_hsa_circ_253586,RMVar_hsa_circ_118773,RMVar_hsa_circ_253597,RMVar_hsa_circ_82244,RMVar_hsa_circ_102984,RMVar_hsa_circ_1563,RMVar_hsa_circ_72522,RMVar_hsa_circ_253598,RMVar_hsa_circ_328522,RMVar_hsa_circ_253602,RMVar_hsa_circ_113218,RMVar_hsa_circ_253603,RMVar_hsa_circ_253604,RMVar_hsa_circ_323136,RMVar_hsa_circ_369494,RMVar_hsa_circ_82034,RMVar_hsa_circ_124342,RMVar_hsa_circ_70436,RMVar_hsa_circ_28556,RMVar_hsa_circ_60421,RMVar_hsa_circ_16794,RMVar_hsa_circ_36080,RMVar_hsa_circ_41203,RMVar_hsa_circ_253605,RMVar_hsa_circ_253607,RMVar_hsa_circ_253608,RMVar_hsa_circ_253606,RMVar_hsa_circ_71062,RMVar_hsa_circ_253612,RMVar_hsa_circ_290820,RMVar_hsa_circ_298167,RMVar_hsa_circ_265668,RMVar_hsa_circ_253611,RMVar_hsa_circ_110210,RMVar_hsa_circ_20006,RMVar_hsa_circ_69591,RMVar_hsa_circ_253613,RMVar_hsa_circ_346202,RMVar_hsa_circ_83156,RMVar_hsa_circ_37805,RMVar_hsa_circ_9133,RMVar_hsa_circ_253616,RMVar_hsa_circ_253617 51110 RMVar_ID_51110 Human_SNP_ID_375599477 A-to-I Human chr8 - 102334564 102334564 102334564 TAACTGGCAGGGCTTGGTGGCTCATGCCTGCAATCCCAGCACTTTGGGAGGCCAAGGCAGACGGA TAACTGGCAGGGCTTGGTGGCTCATGCCTGCATTCCCAGCACTTTGGGAGGCCAAGGCAGACGGA T A UBR5 Ensembl:ENSG00000104517 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935955882 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_288,RMVar_hsa_circ_109109,RMVar_hsa_circ_253586,RMVar_hsa_circ_102984,RMVar_hsa_circ_253604,RMVar_hsa_circ_124342,RMVar_hsa_circ_4094,RMVar_hsa_circ_253605,RMVar_hsa_circ_265668,RMVar_hsa_circ_83156,RMVar_hsa_circ_253617,RMVar_hsa_circ_101744,RMVar_hsa_circ_253618,RMVar_hsa_circ_375189,RMVar_hsa_circ_83002,RMVar_hsa_circ_100046,RMVar_hsa_circ_253630,RMVar_hsa_circ_253631,RMVar_hsa_circ_109439,RMVar_hsa_circ_80339,RMVar_hsa_circ_116187,RMVar_hsa_circ_253635,RMVar_hsa_circ_253634,RMVar_hsa_circ_106734,RMVar_hsa_circ_89894,RMVar_hsa_circ_253638,RMVar_hsa_circ_253639,RMVar_hsa_circ_253636,RMVar_hsa_circ_253637,RMVar_hsa_circ_99472,RMVar_hsa_circ_102449,RMVar_hsa_circ_253650,RMVar_hsa_circ_253651,RMVar_hsa_circ_109958,RMVar_hsa_circ_41598,RMVar_hsa_circ_253656,RMVar_hsa_circ_81131,RMVar_hsa_circ_114757,RMVar_hsa_circ_253659,RMVar_hsa_circ_253661,RMVar_hsa_circ_640,RMVar_hsa_circ_109804,RMVar_hsa_circ_253662,RMVar_hsa_circ_56842,RMVar_hsa_circ_116572,RMVar_hsa_circ_110276,RMVar_hsa_circ_82185,RMVar_hsa_circ_125306,RMVar_hsa_circ_40893,RMVar_hsa_circ_253669,RMVar_hsa_circ_253670,RMVar_hsa_circ_253668,RMVar_hsa_circ_42658,RMVar_hsa_circ_7949,RMVar_hsa_circ_253673,RMVar_hsa_circ_281905,RMVar_hsa_circ_253671,RMVar_hsa_circ_299730,RMVar_hsa_circ_293529,RMVar_hsa_circ_279064,RMVar_hsa_circ_253674,RMVar_hsa_circ_17598,RMVar_hsa_circ_12912,RMVar_hsa_circ_253672,RMVar_hsa_circ_253677,RMVar_hsa_circ_55213,RMVar_hsa_circ_88882,RMVar_hsa_circ_253679,RMVar_hsa_circ_253680,RMVar_hsa_circ_4769,RMVar_hsa_circ_253681,RMVar_hsa_circ_298506,RMVar_hsa_circ_331818,RMVar_hsa_circ_253683,RMVar_hsa_circ_42103,RMVar_hsa_circ_366818,RMVar_hsa_circ_253687,RMVar_hsa_circ_50356,RMVar_hsa_circ_286246,RMVar_hsa_circ_300363,RMVar_hsa_circ_93161,RMVar_hsa_circ_253689,RMVar_hsa_circ_39149,RMVar_hsa_circ_253688,RMVar_hsa_circ_253690,RMVar_hsa_circ_287219,RMVar_hsa_circ_357722,RMVar_hsa_circ_47836,RMVar_hsa_circ_270332,RMVar_hsa_circ_253691,RMVar_hsa_circ_253693,RMVar_hsa_circ_268015,RMVar_hsa_circ_269760 51111 RMVar_ID_51111 Human_SNP_ID_375601911 A-to-I Human chr8 - 102344399 102344399 102344399 TGAGGCAGGAGAATGGCATGAACCCGGGAGGAAGAGCTTGCAGTGAGCTGAGGTGGTACCACTGC TGAGGCAGGAGAATGGCATGAACCCGGGAGGAGGAGCTTGCAGTGAGCTGAGGTGGTACCACTGC T C UBR5 Ensembl:ENSG00000104517 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1371988926 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_288,RMVar_hsa_circ_109109,RMVar_hsa_circ_253586,RMVar_hsa_circ_102984,RMVar_hsa_circ_253604,RMVar_hsa_circ_124342,RMVar_hsa_circ_4094,RMVar_hsa_circ_253605,RMVar_hsa_circ_265668,RMVar_hsa_circ_83156,RMVar_hsa_circ_253617,RMVar_hsa_circ_101744,RMVar_hsa_circ_253618,RMVar_hsa_circ_375189,RMVar_hsa_circ_83002,RMVar_hsa_circ_100046,RMVar_hsa_circ_253630,RMVar_hsa_circ_253631,RMVar_hsa_circ_109439,RMVar_hsa_circ_80339,RMVar_hsa_circ_116187,RMVar_hsa_circ_253635,RMVar_hsa_circ_253634,RMVar_hsa_circ_89894,RMVar_hsa_circ_253638,RMVar_hsa_circ_253636,RMVar_hsa_circ_253637,RMVar_hsa_circ_99472,RMVar_hsa_circ_102449,RMVar_hsa_circ_253650,RMVar_hsa_circ_253651,RMVar_hsa_circ_109958,RMVar_hsa_circ_41598,RMVar_hsa_circ_253656,RMVar_hsa_circ_81131,RMVar_hsa_circ_114757,RMVar_hsa_circ_253659,RMVar_hsa_circ_253661,RMVar_hsa_circ_640,RMVar_hsa_circ_109804,RMVar_hsa_circ_253662,RMVar_hsa_circ_56842,RMVar_hsa_circ_116572,RMVar_hsa_circ_110276,RMVar_hsa_circ_82185,RMVar_hsa_circ_125306,RMVar_hsa_circ_40893,RMVar_hsa_circ_253669,RMVar_hsa_circ_253670,RMVar_hsa_circ_253668,RMVar_hsa_circ_7949,RMVar_hsa_circ_253673,RMVar_hsa_circ_281905,RMVar_hsa_circ_253671,RMVar_hsa_circ_299730,RMVar_hsa_circ_293529,RMVar_hsa_circ_279064,RMVar_hsa_circ_253674,RMVar_hsa_circ_17598,RMVar_hsa_circ_12912,RMVar_hsa_circ_253672,RMVar_hsa_circ_253677,RMVar_hsa_circ_55213,RMVar_hsa_circ_88882,RMVar_hsa_circ_253679,RMVar_hsa_circ_253680,RMVar_hsa_circ_4769,RMVar_hsa_circ_253681,RMVar_hsa_circ_298506,RMVar_hsa_circ_331818,RMVar_hsa_circ_253683,RMVar_hsa_circ_366818,RMVar_hsa_circ_12024,RMVar_hsa_circ_253687,RMVar_hsa_circ_50356,RMVar_hsa_circ_286246,RMVar_hsa_circ_300363,RMVar_hsa_circ_93161,RMVar_hsa_circ_253689,RMVar_hsa_circ_39149,RMVar_hsa_circ_253688,RMVar_hsa_circ_253690,RMVar_hsa_circ_287219,RMVar_hsa_circ_357722,RMVar_hsa_circ_270332,RMVar_hsa_circ_253691,RMVar_hsa_circ_268015,RMVar_hsa_circ_269760,RMVar_hsa_circ_278530,RMVar_hsa_circ_312994,RMVar_hsa_circ_356428,RMVar_hsa_circ_294684,RMVar_hsa_circ_60616,RMVar_hsa_circ_253695,RMVar_hsa_circ_253696,RMVar_hsa_circ_253694 51112 RMVar_ID_51112 Human_SNP_ID_375602005 A-to-I Human chr8 - 102344746 102344746 102344746 TTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTAGCCAGGCTGGTCTTGAACTCCTGACCT TTTTGTATTTTTAGTAGAGACGGGGTTTCACCTTGTTAGCCAGGCTGGTCTTGAACTCCTGACCT T A UBR5 Ensembl:ENSG00000104517 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs960803187 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_288,RMVar_hsa_circ_109109,RMVar_hsa_circ_253586,RMVar_hsa_circ_102984,RMVar_hsa_circ_253604,RMVar_hsa_circ_124342,RMVar_hsa_circ_4094,RMVar_hsa_circ_253605,RMVar_hsa_circ_265668,RMVar_hsa_circ_83156,RMVar_hsa_circ_253617,RMVar_hsa_circ_101744,RMVar_hsa_circ_253618,RMVar_hsa_circ_375189,RMVar_hsa_circ_83002,RMVar_hsa_circ_100046,RMVar_hsa_circ_253630,RMVar_hsa_circ_253631,RMVar_hsa_circ_109439,RMVar_hsa_circ_80339,RMVar_hsa_circ_116187,RMVar_hsa_circ_253635,RMVar_hsa_circ_253634,RMVar_hsa_circ_89894,RMVar_hsa_circ_253638,RMVar_hsa_circ_253636,RMVar_hsa_circ_253637,RMVar_hsa_circ_99472,RMVar_hsa_circ_102449,RMVar_hsa_circ_253650,RMVar_hsa_circ_253651,RMVar_hsa_circ_109958,RMVar_hsa_circ_41598,RMVar_hsa_circ_253656,RMVar_hsa_circ_81131,RMVar_hsa_circ_114757,RMVar_hsa_circ_253659,RMVar_hsa_circ_253661,RMVar_hsa_circ_640,RMVar_hsa_circ_109804,RMVar_hsa_circ_253662,RMVar_hsa_circ_56842,RMVar_hsa_circ_116572,RMVar_hsa_circ_110276,RMVar_hsa_circ_82185,RMVar_hsa_circ_125306,RMVar_hsa_circ_40893,RMVar_hsa_circ_253669,RMVar_hsa_circ_253670,RMVar_hsa_circ_253668,RMVar_hsa_circ_7949,RMVar_hsa_circ_253673,RMVar_hsa_circ_281905,RMVar_hsa_circ_253671,RMVar_hsa_circ_299730,RMVar_hsa_circ_293529,RMVar_hsa_circ_279064,RMVar_hsa_circ_253674,RMVar_hsa_circ_17598,RMVar_hsa_circ_12912,RMVar_hsa_circ_253672,RMVar_hsa_circ_253677,RMVar_hsa_circ_55213,RMVar_hsa_circ_88882,RMVar_hsa_circ_253679,RMVar_hsa_circ_253680,RMVar_hsa_circ_4769,RMVar_hsa_circ_253681,RMVar_hsa_circ_298506,RMVar_hsa_circ_331818,RMVar_hsa_circ_253683,RMVar_hsa_circ_366818,RMVar_hsa_circ_12024,RMVar_hsa_circ_253687,RMVar_hsa_circ_50356,RMVar_hsa_circ_286246,RMVar_hsa_circ_300363,RMVar_hsa_circ_93161,RMVar_hsa_circ_253689,RMVar_hsa_circ_39149,RMVar_hsa_circ_253688,RMVar_hsa_circ_253690,RMVar_hsa_circ_287219,RMVar_hsa_circ_357722,RMVar_hsa_circ_270332,RMVar_hsa_circ_253691,RMVar_hsa_circ_268015,RMVar_hsa_circ_269760,RMVar_hsa_circ_278530,RMVar_hsa_circ_312994,RMVar_hsa_circ_356428,RMVar_hsa_circ_294684,RMVar_hsa_circ_60616,RMVar_hsa_circ_253695,RMVar_hsa_circ_253696,RMVar_hsa_circ_253694 51113 RMVar_ID_51113 Human_SNP_ID_375602006 A-to-I Human chr8 - 102344746 102344746 102344746 TTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTAGCCAGGCTGGTCTTGAACTCCTGACCT TTTTGTATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGCTGGTCTTGAACTCCTGACCT T C UBR5 Ensembl:ENSG00000104517 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs960803187 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_288,RMVar_hsa_circ_109109,RMVar_hsa_circ_253586,RMVar_hsa_circ_102984,RMVar_hsa_circ_253604,RMVar_hsa_circ_124342,RMVar_hsa_circ_4094,RMVar_hsa_circ_253605,RMVar_hsa_circ_265668,RMVar_hsa_circ_83156,RMVar_hsa_circ_253617,RMVar_hsa_circ_101744,RMVar_hsa_circ_253618,RMVar_hsa_circ_375189,RMVar_hsa_circ_83002,RMVar_hsa_circ_100046,RMVar_hsa_circ_253630,RMVar_hsa_circ_253631,RMVar_hsa_circ_109439,RMVar_hsa_circ_80339,RMVar_hsa_circ_116187,RMVar_hsa_circ_253635,RMVar_hsa_circ_253634,RMVar_hsa_circ_89894,RMVar_hsa_circ_253638,RMVar_hsa_circ_253636,RMVar_hsa_circ_253637,RMVar_hsa_circ_99472,RMVar_hsa_circ_102449,RMVar_hsa_circ_253650,RMVar_hsa_circ_253651,RMVar_hsa_circ_109958,RMVar_hsa_circ_41598,RMVar_hsa_circ_253656,RMVar_hsa_circ_81131,RMVar_hsa_circ_114757,RMVar_hsa_circ_253659,RMVar_hsa_circ_253661,RMVar_hsa_circ_640,RMVar_hsa_circ_109804,RMVar_hsa_circ_253662,RMVar_hsa_circ_56842,RMVar_hsa_circ_116572,RMVar_hsa_circ_110276,RMVar_hsa_circ_82185,RMVar_hsa_circ_125306,RMVar_hsa_circ_40893,RMVar_hsa_circ_253669,RMVar_hsa_circ_253670,RMVar_hsa_circ_253668,RMVar_hsa_circ_7949,RMVar_hsa_circ_253673,RMVar_hsa_circ_281905,RMVar_hsa_circ_253671,RMVar_hsa_circ_299730,RMVar_hsa_circ_293529,RMVar_hsa_circ_279064,RMVar_hsa_circ_253674,RMVar_hsa_circ_17598,RMVar_hsa_circ_12912,RMVar_hsa_circ_253672,RMVar_hsa_circ_253677,RMVar_hsa_circ_55213,RMVar_hsa_circ_88882,RMVar_hsa_circ_253679,RMVar_hsa_circ_253680,RMVar_hsa_circ_4769,RMVar_hsa_circ_253681,RMVar_hsa_circ_298506,RMVar_hsa_circ_331818,RMVar_hsa_circ_253683,RMVar_hsa_circ_366818,RMVar_hsa_circ_12024,RMVar_hsa_circ_253687,RMVar_hsa_circ_50356,RMVar_hsa_circ_286246,RMVar_hsa_circ_300363,RMVar_hsa_circ_93161,RMVar_hsa_circ_253689,RMVar_hsa_circ_39149,RMVar_hsa_circ_253688,RMVar_hsa_circ_253690,RMVar_hsa_circ_287219,RMVar_hsa_circ_357722,RMVar_hsa_circ_270332,RMVar_hsa_circ_253691,RMVar_hsa_circ_268015,RMVar_hsa_circ_269760,RMVar_hsa_circ_278530,RMVar_hsa_circ_312994,RMVar_hsa_circ_356428,RMVar_hsa_circ_294684,RMVar_hsa_circ_60616,RMVar_hsa_circ_253695,RMVar_hsa_circ_253696,RMVar_hsa_circ_253694 51114 RMVar_ID_51114 Human_SNP_ID_375602007 A-to-I Human chr8 - 102344746 102344746 102344746 TTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTAGCCAGGCTGGTCTTGAACTCCTGACCT TTTTGTATTTTTAGTAGAGACGGGGTTTCACCCTGTTAGCCAGGCTGGTCTTGAACTCCTGACCT T G UBR5 Ensembl:ENSG00000104517 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs960803187 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_288,RMVar_hsa_circ_109109,RMVar_hsa_circ_253586,RMVar_hsa_circ_102984,RMVar_hsa_circ_253604,RMVar_hsa_circ_124342,RMVar_hsa_circ_4094,RMVar_hsa_circ_253605,RMVar_hsa_circ_265668,RMVar_hsa_circ_83156,RMVar_hsa_circ_253617,RMVar_hsa_circ_101744,RMVar_hsa_circ_253618,RMVar_hsa_circ_375189,RMVar_hsa_circ_83002,RMVar_hsa_circ_100046,RMVar_hsa_circ_253630,RMVar_hsa_circ_253631,RMVar_hsa_circ_109439,RMVar_hsa_circ_80339,RMVar_hsa_circ_116187,RMVar_hsa_circ_253635,RMVar_hsa_circ_253634,RMVar_hsa_circ_89894,RMVar_hsa_circ_253638,RMVar_hsa_circ_253636,RMVar_hsa_circ_253637,RMVar_hsa_circ_99472,RMVar_hsa_circ_102449,RMVar_hsa_circ_253650,RMVar_hsa_circ_253651,RMVar_hsa_circ_109958,RMVar_hsa_circ_41598,RMVar_hsa_circ_253656,RMVar_hsa_circ_81131,RMVar_hsa_circ_114757,RMVar_hsa_circ_253659,RMVar_hsa_circ_253661,RMVar_hsa_circ_640,RMVar_hsa_circ_109804,RMVar_hsa_circ_253662,RMVar_hsa_circ_56842,RMVar_hsa_circ_116572,RMVar_hsa_circ_110276,RMVar_hsa_circ_82185,RMVar_hsa_circ_125306,RMVar_hsa_circ_40893,RMVar_hsa_circ_253669,RMVar_hsa_circ_253670,RMVar_hsa_circ_253668,RMVar_hsa_circ_7949,RMVar_hsa_circ_253673,RMVar_hsa_circ_281905,RMVar_hsa_circ_253671,RMVar_hsa_circ_299730,RMVar_hsa_circ_293529,RMVar_hsa_circ_279064,RMVar_hsa_circ_253674,RMVar_hsa_circ_17598,RMVar_hsa_circ_12912,RMVar_hsa_circ_253672,RMVar_hsa_circ_253677,RMVar_hsa_circ_55213,RMVar_hsa_circ_88882,RMVar_hsa_circ_253679,RMVar_hsa_circ_253680,RMVar_hsa_circ_4769,RMVar_hsa_circ_253681,RMVar_hsa_circ_298506,RMVar_hsa_circ_331818,RMVar_hsa_circ_253683,RMVar_hsa_circ_366818,RMVar_hsa_circ_12024,RMVar_hsa_circ_253687,RMVar_hsa_circ_50356,RMVar_hsa_circ_286246,RMVar_hsa_circ_300363,RMVar_hsa_circ_93161,RMVar_hsa_circ_253689,RMVar_hsa_circ_39149,RMVar_hsa_circ_253688,RMVar_hsa_circ_253690,RMVar_hsa_circ_287219,RMVar_hsa_circ_357722,RMVar_hsa_circ_270332,RMVar_hsa_circ_253691,RMVar_hsa_circ_268015,RMVar_hsa_circ_269760,RMVar_hsa_circ_278530,RMVar_hsa_circ_312994,RMVar_hsa_circ_356428,RMVar_hsa_circ_294684,RMVar_hsa_circ_60616,RMVar_hsa_circ_253695,RMVar_hsa_circ_253696,RMVar_hsa_circ_253694 51115 RMVar_ID_51115 Human_SNP_ID_375602023 A-to-I Human chr8 - 102344807 102344807 102344807 CTCCTGCCTCAGCCTCCTGAGTAGCTGAAATTACAGGTGCCTGCCACCATGTCCAGTTAATTTTT CTCCTGCCTCAGCCTCCTGAGTAGCTGAAATTGCAGGTGCCTGCCACCATGTCCAGTTAATTTTT T C UBR5 Ensembl:ENSG00000104517 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1477437910 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_288,RMVar_hsa_circ_109109,RMVar_hsa_circ_253586,RMVar_hsa_circ_102984,RMVar_hsa_circ_253604,RMVar_hsa_circ_124342,RMVar_hsa_circ_4094,RMVar_hsa_circ_253605,RMVar_hsa_circ_265668,RMVar_hsa_circ_83156,RMVar_hsa_circ_253617,RMVar_hsa_circ_101744,RMVar_hsa_circ_253618,RMVar_hsa_circ_375189,RMVar_hsa_circ_83002,RMVar_hsa_circ_100046,RMVar_hsa_circ_253630,RMVar_hsa_circ_253631,RMVar_hsa_circ_109439,RMVar_hsa_circ_80339,RMVar_hsa_circ_116187,RMVar_hsa_circ_253635,RMVar_hsa_circ_253634,RMVar_hsa_circ_89894,RMVar_hsa_circ_253638,RMVar_hsa_circ_253636,RMVar_hsa_circ_253637,RMVar_hsa_circ_99472,RMVar_hsa_circ_102449,RMVar_hsa_circ_253650,RMVar_hsa_circ_253651,RMVar_hsa_circ_109958,RMVar_hsa_circ_41598,RMVar_hsa_circ_253656,RMVar_hsa_circ_81131,RMVar_hsa_circ_114757,RMVar_hsa_circ_253659,RMVar_hsa_circ_253661,RMVar_hsa_circ_640,RMVar_hsa_circ_109804,RMVar_hsa_circ_253662,RMVar_hsa_circ_56842,RMVar_hsa_circ_116572,RMVar_hsa_circ_110276,RMVar_hsa_circ_82185,RMVar_hsa_circ_125306,RMVar_hsa_circ_40893,RMVar_hsa_circ_253669,RMVar_hsa_circ_253670,RMVar_hsa_circ_253668,RMVar_hsa_circ_7949,RMVar_hsa_circ_253673,RMVar_hsa_circ_281905,RMVar_hsa_circ_253671,RMVar_hsa_circ_299730,RMVar_hsa_circ_293529,RMVar_hsa_circ_279064,RMVar_hsa_circ_253674,RMVar_hsa_circ_17598,RMVar_hsa_circ_12912,RMVar_hsa_circ_253672,RMVar_hsa_circ_253677,RMVar_hsa_circ_55213,RMVar_hsa_circ_88882,RMVar_hsa_circ_253679,RMVar_hsa_circ_253680,RMVar_hsa_circ_4769,RMVar_hsa_circ_253681,RMVar_hsa_circ_298506,RMVar_hsa_circ_331818,RMVar_hsa_circ_253683,RMVar_hsa_circ_366818,RMVar_hsa_circ_12024,RMVar_hsa_circ_253687,RMVar_hsa_circ_50356,RMVar_hsa_circ_286246,RMVar_hsa_circ_300363,RMVar_hsa_circ_93161,RMVar_hsa_circ_253689,RMVar_hsa_circ_39149,RMVar_hsa_circ_253688,RMVar_hsa_circ_253690,RMVar_hsa_circ_287219,RMVar_hsa_circ_357722,RMVar_hsa_circ_270332,RMVar_hsa_circ_253691,RMVar_hsa_circ_268015,RMVar_hsa_circ_269760,RMVar_hsa_circ_278530,RMVar_hsa_circ_312994,RMVar_hsa_circ_356428,RMVar_hsa_circ_294684,RMVar_hsa_circ_60616,RMVar_hsa_circ_253695,RMVar_hsa_circ_253696,RMVar_hsa_circ_253694 51116 RMVar_ID_51116 Human_SNP_ID_375605134 A-to-I Human chr8 - 102357456 102357456 102357456 GACTTAATGCAATCCTCCTGCCTCAGCCTCCCAAGTAGCTAGGATGTAGGTATGGGCCACCACCA GACTTAATGCAATCCTCCTGCCTCAGCCTCCCTAGTAGCTAGGATGTAGGTATGGGCCACCACCA T A UBR5 Ensembl:ENSG00000104517 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256764214 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16304455 RMVar_hsa_circ_109109,RMVar_hsa_circ_253586,RMVar_hsa_circ_102984,RMVar_hsa_circ_253604,RMVar_hsa_circ_100046,RMVar_hsa_circ_80339,RMVar_hsa_circ_253635,RMVar_hsa_circ_89894,RMVar_hsa_circ_253636,RMVar_hsa_circ_253637,RMVar_hsa_circ_114757,RMVar_hsa_circ_253661,RMVar_hsa_circ_56842,RMVar_hsa_circ_82185,RMVar_hsa_circ_253670,RMVar_hsa_circ_7949,RMVar_hsa_circ_281905,RMVar_hsa_circ_17598,RMVar_hsa_circ_12912,RMVar_hsa_circ_55213,RMVar_hsa_circ_88882,RMVar_hsa_circ_253679,RMVar_hsa_circ_4769,RMVar_hsa_circ_253681,RMVar_hsa_circ_331818,RMVar_hsa_circ_366818,RMVar_hsa_circ_50356,RMVar_hsa_circ_93161,RMVar_hsa_circ_253689,RMVar_hsa_circ_268015,RMVar_hsa_circ_356428,RMVar_hsa_circ_294684,RMVar_hsa_circ_60616,RMVar_hsa_circ_3425,RMVar_hsa_circ_110662,RMVar_hsa_circ_253696,RMVar_hsa_circ_324057,RMVar_hsa_circ_374958,RMVar_hsa_circ_115812,RMVar_hsa_circ_114465,RMVar_hsa_circ_253699,RMVar_hsa_circ_253701,RMVar_hsa_circ_253700,RMVar_hsa_circ_253697,RMVar_hsa_circ_253698,RMVar_hsa_circ_300742,RMVar_hsa_circ_77218,RMVar_hsa_circ_253707,RMVar_hsa_circ_253708,RMVar_hsa_circ_268226 51117 RMVar_ID_51117 Human_SNP_ID_375605147 A-to-I Human chr8 - 102357505 102357505 102357505 GCCAGAGGGCAGTGGCACAATGATAACTCACTATAACCTTGAACTCCTGGACTTAATGCAATCCT GCCAGAGGGCAGTGGCACAATGATAACTCACTGTAACCTTGAACTCCTGGACTTAATGCAATCCT T C UBR5 Ensembl:ENSG00000104517 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs949235908 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7793940,Human_RBP_ID_16304456 RMVar_hsa_circ_109109,RMVar_hsa_circ_253586,RMVar_hsa_circ_102984,RMVar_hsa_circ_253604,RMVar_hsa_circ_100046,RMVar_hsa_circ_80339,RMVar_hsa_circ_253635,RMVar_hsa_circ_89894,RMVar_hsa_circ_253636,RMVar_hsa_circ_253637,RMVar_hsa_circ_114757,RMVar_hsa_circ_253661,RMVar_hsa_circ_56842,RMVar_hsa_circ_82185,RMVar_hsa_circ_253670,RMVar_hsa_circ_7949,RMVar_hsa_circ_281905,RMVar_hsa_circ_17598,RMVar_hsa_circ_12912,RMVar_hsa_circ_55213,RMVar_hsa_circ_88882,RMVar_hsa_circ_253679,RMVar_hsa_circ_4769,RMVar_hsa_circ_253681,RMVar_hsa_circ_331818,RMVar_hsa_circ_366818,RMVar_hsa_circ_50356,RMVar_hsa_circ_93161,RMVar_hsa_circ_253689,RMVar_hsa_circ_268015,RMVar_hsa_circ_356428,RMVar_hsa_circ_294684,RMVar_hsa_circ_60616,RMVar_hsa_circ_3425,RMVar_hsa_circ_110662,RMVar_hsa_circ_253696,RMVar_hsa_circ_324057,RMVar_hsa_circ_374958,RMVar_hsa_circ_115812,RMVar_hsa_circ_114465,RMVar_hsa_circ_253699,RMVar_hsa_circ_253701,RMVar_hsa_circ_253700,RMVar_hsa_circ_253697,RMVar_hsa_circ_253698,RMVar_hsa_circ_300742,RMVar_hsa_circ_77218,RMVar_hsa_circ_253707,RMVar_hsa_circ_253708,RMVar_hsa_circ_268226 51118 RMVar_ID_51118 Human_SNP_ID_375605150 A-to-I Human chr8 - 102357513 102357513 102357513 TTGCCCAGGCCAGAGGGCAGTGGCACAATGATAACTCACTATAACCTTGAACTCCTGGACTTAAT TTGCCCAGGCCAGAGGGCAGTGGCACAATGATGACTCACTATAACCTTGAACTCCTGGACTTAAT T C UBR5 Ensembl:ENSG00000104517 Protein coding intron GSE107867 ASD brains,frontal_cortex;ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1403912036 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7793941,Human_RBP_ID_16304456 RMVar_hsa_circ_109109,RMVar_hsa_circ_253586,RMVar_hsa_circ_102984,RMVar_hsa_circ_253604,RMVar_hsa_circ_100046,RMVar_hsa_circ_80339,RMVar_hsa_circ_253635,RMVar_hsa_circ_89894,RMVar_hsa_circ_253636,RMVar_hsa_circ_253637,RMVar_hsa_circ_114757,RMVar_hsa_circ_253661,RMVar_hsa_circ_56842,RMVar_hsa_circ_82185,RMVar_hsa_circ_253670,RMVar_hsa_circ_7949,RMVar_hsa_circ_281905,RMVar_hsa_circ_17598,RMVar_hsa_circ_12912,RMVar_hsa_circ_55213,RMVar_hsa_circ_88882,RMVar_hsa_circ_253679,RMVar_hsa_circ_4769,RMVar_hsa_circ_253681,RMVar_hsa_circ_331818,RMVar_hsa_circ_366818,RMVar_hsa_circ_50356,RMVar_hsa_circ_93161,RMVar_hsa_circ_253689,RMVar_hsa_circ_268015,RMVar_hsa_circ_356428,RMVar_hsa_circ_294684,RMVar_hsa_circ_60616,RMVar_hsa_circ_3425,RMVar_hsa_circ_110662,RMVar_hsa_circ_253696,RMVar_hsa_circ_324057,RMVar_hsa_circ_374958,RMVar_hsa_circ_115812,RMVar_hsa_circ_114465,RMVar_hsa_circ_253699,RMVar_hsa_circ_253701,RMVar_hsa_circ_253700,RMVar_hsa_circ_253697,RMVar_hsa_circ_253698,RMVar_hsa_circ_300742,RMVar_hsa_circ_77218,RMVar_hsa_circ_253707,RMVar_hsa_circ_253708,RMVar_hsa_circ_268226 51119 RMVar_ID_51119 Human_SNP_ID_375605255 A-to-I Human chr8 - 102357966 102357966 102357966 AATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATTTTGGCCAGGTTGGTCTTGAACTCCGGA AATTTTTGTATTTTTAGTAGAGACAGGGTTTCCCCATTTTGGCCAGGTTGGTCTTGAACTCCGGA T G UBR5 Ensembl:ENSG00000104517 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1293919487 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16304482 RMVar_hsa_circ_109109,RMVar_hsa_circ_253586,RMVar_hsa_circ_102984,RMVar_hsa_circ_253604,RMVar_hsa_circ_100046,RMVar_hsa_circ_80339,RMVar_hsa_circ_253635,RMVar_hsa_circ_89894,RMVar_hsa_circ_253636,RMVar_hsa_circ_253637,RMVar_hsa_circ_114757,RMVar_hsa_circ_253661,RMVar_hsa_circ_56842,RMVar_hsa_circ_82185,RMVar_hsa_circ_253670,RMVar_hsa_circ_7949,RMVar_hsa_circ_281905,RMVar_hsa_circ_17598,RMVar_hsa_circ_12912,RMVar_hsa_circ_55213,RMVar_hsa_circ_88882,RMVar_hsa_circ_253679,RMVar_hsa_circ_4769,RMVar_hsa_circ_253681,RMVar_hsa_circ_331818,RMVar_hsa_circ_366818,RMVar_hsa_circ_50356,RMVar_hsa_circ_93161,RMVar_hsa_circ_253689,RMVar_hsa_circ_268015,RMVar_hsa_circ_356428,RMVar_hsa_circ_294684,RMVar_hsa_circ_60616,RMVar_hsa_circ_3425,RMVar_hsa_circ_110662,RMVar_hsa_circ_253696,RMVar_hsa_circ_324057,RMVar_hsa_circ_374958,RMVar_hsa_circ_115812,RMVar_hsa_circ_114465,RMVar_hsa_circ_253699,RMVar_hsa_circ_253701,RMVar_hsa_circ_253700,RMVar_hsa_circ_253697,RMVar_hsa_circ_253698,RMVar_hsa_circ_300742,RMVar_hsa_circ_77218,RMVar_hsa_circ_253707,RMVar_hsa_circ_253708,RMVar_hsa_circ_268226 51120 RMVar_ID_51120 Human_SNP_ID_375605507 A-to-I Human chr8 - 102358933 102358933 102358933 CATTTTTACTAAAAATACAAAAATGTAGCTGAATGTGGTGGCGCATGCCTGTAGTCCTAGCTACC CATTTTTACTAAAAATACAAAAATGTAGCTGATTGTGGTGGCGCATGCCTGTAGTCCTAGCTACC T A UBR5 Ensembl:ENSG00000104517 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1380373427 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_109109,RMVar_hsa_circ_253586,RMVar_hsa_circ_102984,RMVar_hsa_circ_253604,RMVar_hsa_circ_100046,RMVar_hsa_circ_80339,RMVar_hsa_circ_253635,RMVar_hsa_circ_89894,RMVar_hsa_circ_253636,RMVar_hsa_circ_253637,RMVar_hsa_circ_114757,RMVar_hsa_circ_253661,RMVar_hsa_circ_56842,RMVar_hsa_circ_82185,RMVar_hsa_circ_253670,RMVar_hsa_circ_7949,RMVar_hsa_circ_281905,RMVar_hsa_circ_17598,RMVar_hsa_circ_12912,RMVar_hsa_circ_55213,RMVar_hsa_circ_88882,RMVar_hsa_circ_253679,RMVar_hsa_circ_4769,RMVar_hsa_circ_253681,RMVar_hsa_circ_331818,RMVar_hsa_circ_366818,RMVar_hsa_circ_50356,RMVar_hsa_circ_93161,RMVar_hsa_circ_253689,RMVar_hsa_circ_268015,RMVar_hsa_circ_356428,RMVar_hsa_circ_294684,RMVar_hsa_circ_60616,RMVar_hsa_circ_3425,RMVar_hsa_circ_110662,RMVar_hsa_circ_253696,RMVar_hsa_circ_324057,RMVar_hsa_circ_374958,RMVar_hsa_circ_115812,RMVar_hsa_circ_114465,RMVar_hsa_circ_253699,RMVar_hsa_circ_253701,RMVar_hsa_circ_253700,RMVar_hsa_circ_253697,RMVar_hsa_circ_253698,RMVar_hsa_circ_300742,RMVar_hsa_circ_77218,RMVar_hsa_circ_253707,RMVar_hsa_circ_253708,RMVar_hsa_circ_268226 51121 RMVar_ID_51121 Human_SNP_ID_375611883 A-to-I Human chr8 - 102384535 102384512 102384536 CACCATGCCCAGCTAATTTTTAAATTTTTTGTAGAGACGGGGTCTCATTATGTTGCCCACATTAG CACCATGCCCAGCTAATTTTTAAATTTTTTG________________________CCCACATTAG GCAACATAATGAGACCCCGTCTCTA G UBR5 Ensembl:ENSG00000104517 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs561761215 Functional Loss DEL dbSNP153 32..55 33 - - - Human_RBP_ID_16506154 RMVar_hsa_circ_100046,RMVar_hsa_circ_253635,RMVar_hsa_circ_115812,RMVar_hsa_circ_253697,RMVar_hsa_circ_77218,RMVar_hsa_circ_253708 51122 RMVar_ID_51122 Human_SNP_ID_375611891 A-to-I Human chr8 - 102384535 102384535 102384535 CACCATGCCCAGCTAATTTTTAAATTTTTTGTAGAGACGGGGTCTCATTATGTTGCCCACATTAG CACCATGCCCAGCTAATTTTTAAATTTTTTGTGGAGACGGGGTCTCATTATGTTGCCCACATTAG T C UBR5 Ensembl:ENSG00000104517 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1171733395 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16506154 RMVar_hsa_circ_100046,RMVar_hsa_circ_253635,RMVar_hsa_circ_115812,RMVar_hsa_circ_253697,RMVar_hsa_circ_77218,RMVar_hsa_circ_253708 51123 RMVar_ID_51123 Human_SNP_ID_375614247 A-to-I Human chr8 - 102393469 102393469 102393469 ACCATGCGTGGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCACGCTGG ACCATGCGTGGCTAATTTTTTGTATTTTTAGTGGAGACGGGGTTTCACCATGTTGGCCACGCTGG T C UBR5 Ensembl:ENSG00000104517 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs553334357 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100046,RMVar_hsa_circ_253635,RMVar_hsa_circ_115812,RMVar_hsa_circ_253697,RMVar_hsa_circ_77218,RMVar_hsa_circ_253708 51124 RMVar_ID_51124 Human_SNP_ID_375614249 A-to-I Human chr8 - 102393478 102393478 102393478 GCGTGTGCTACCATGCGTGGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGG GCGTGTGCTACCATGCGTGGCTAATTTTTTGTGTTTTTAGTAGAGACGGGGTTTCACCATGTTGG T C UBR5 Ensembl:ENSG00000104517 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs924348643 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100046,RMVar_hsa_circ_253635,RMVar_hsa_circ_115812,RMVar_hsa_circ_253697,RMVar_hsa_circ_77218,RMVar_hsa_circ_253708 51125 RMVar_ID_51125 Human_SNP_ID_375614329 A-to-I Human chr8 - 102393738 102393738 102393738 TTTAGTAGAGATGGAGTTTCACCATGCTGGCCAGGCTGGTCTCGAACTCCTGGCCTCAAGTGATC TTTAGTAGAGATGGAGTTTCACCATGCTGGCCCGGCTGGTCTCGAACTCCTGGCCTCAAGTGATC T G UBR5 Ensembl:ENSG00000104517 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs968795673 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16305892 RMVar_hsa_circ_100046,RMVar_hsa_circ_253635,RMVar_hsa_circ_115812,RMVar_hsa_circ_253697,RMVar_hsa_circ_77218,RMVar_hsa_circ_253708 51126 RMVar_ID_51126 Human_SNP_ID_375614618 A-to-I Human chr8 - 102394965 102394965 102394965 CTAAAAGAAGCCCAGAATGCTTAGACTGATGAATACATAGAGTTTCAAATCAGTTGAATAATGTT CTAAAAGAAGCCCAGAATGCTTAGACTGATGAGTACATAGAGTTTCAAATCAGTTGAATAATGTT T C UBR5 Ensembl:ENSG00000104517 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs4495397 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3128880,Human_RBP_ID_16305922 GWAS_ID_6602,GWAS_ID_6603 RMVar_hsa_circ_100046,RMVar_hsa_circ_253635,RMVar_hsa_circ_115812,RMVar_hsa_circ_253697,RMVar_hsa_circ_77218,RMVar_hsa_circ_253708 51127 RMVar_ID_51127 Human_SNP_ID_375615786 A-to-I Human chr8 - 102399544 102399544 102399544 GGCTGGGCATAATGGCTCACGCCTGTAATCTCAGCACTTTGGGAGGCCGAAGCTGGCTGATCACC GGCTGGGCATAATGGCTCACGCCTGTAATCTCGGCACTTTGGGAGGCCGAAGCTGGCTGATCACC T C UBR5 Ensembl:ENSG00000104517 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1048324839 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16306103,Human_RBP_ID_17578697 RMVar_hsa_circ_100046,RMVar_hsa_circ_253635,RMVar_hsa_circ_115812,RMVar_hsa_circ_253697,RMVar_hsa_circ_77218,RMVar_hsa_circ_253708 51128 RMVar_ID_51128 Human_SNP_ID_375615976 A-to-I Human chr8 - 102400229 102400229 102400229 CTAGGCTGATCTTGAACTCCTGGGCTCAAGCAACCCTCTTGCCTCAGCTTCCTGAGTAGCTGGGA CTAGGCTGATCTTGAACTCCTGGGCTCAAGCATCCCTCTTGCCTCAGCTTCCTGAGTAGCTGGGA T A UBR5 Ensembl:ENSG00000104517 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs999947560 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100046,RMVar_hsa_circ_253635,RMVar_hsa_circ_115812,RMVar_hsa_circ_253697,RMVar_hsa_circ_77218,RMVar_hsa_circ_253708 51129 RMVar_ID_51129 Human_SNP_ID_375615977 A-to-I Human chr8 - 102400229 102400229 102400229 CTAGGCTGATCTTGAACTCCTGGGCTCAAGCAACCCTCTTGCCTCAGCTTCCTGAGTAGCTGGGA CTAGGCTGATCTTGAACTCCTGGGCTCAAGCAGCCCTCTTGCCTCAGCTTCCTGAGTAGCTGGGA T C UBR5 Ensembl:ENSG00000104517 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs999947560 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100046,RMVar_hsa_circ_253635,RMVar_hsa_circ_115812,RMVar_hsa_circ_253697,RMVar_hsa_circ_77218,RMVar_hsa_circ_253708 51130 RMVar_ID_51130 Human_SNP_ID_375615978 A-to-I Human chr8 - 102400229 102400229 102400229 CTAGGCTGATCTTGAACTCCTGGGCTCAAGCAACCCTCTTGCCTCAGCTTCCTGAGTAGCTGGGA CTAGGCTGATCTTGAACTCCTGGGCTCAAGCACCCCTCTTGCCTCAGCTTCCTGAGTAGCTGGGA T G UBR5 Ensembl:ENSG00000104517 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs999947560 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100046,RMVar_hsa_circ_253635,RMVar_hsa_circ_115812,RMVar_hsa_circ_253697,RMVar_hsa_circ_77218,RMVar_hsa_circ_253708 51131 RMVar_ID_51131 Human_SNP_ID_375617350 A-to-I Human chr8 - 102405820 102405820 102405820 CATTTTATCATACATATTTATTTTGTTTTTTGAGTCTCGCTCTTGCCCACGCTGGAATGCAGTGG CATTTTATCATACATATTTATTTTGTTTTTTGTGTCTCGCTCTTGCCCACGCTGGAATGCAGTGG T A UBR5 Ensembl:ENSG00000104517 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1000928781 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16506248 RMVar_hsa_circ_100046,RMVar_hsa_circ_253635,RMVar_hsa_circ_115812,RMVar_hsa_circ_253697,RMVar_hsa_circ_77218,RMVar_hsa_circ_253708 51132 RMVar_ID_51132 Human_SNP_ID_375617804 A-to-I Human chr8 - 102407600 102407600 102407600 TACCACTATGTCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCGTCATGTTGGCTAGGC TACCACTATGTCTGGCTAATTTTTGTATTTTTGGTAGAGATGGGGTTTCGTCATGTTGGCTAGGC T C UBR5 Ensembl:ENSG00000104517 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs754073586 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_100046,RMVar_hsa_circ_253635,RMVar_hsa_circ_115812,RMVar_hsa_circ_253697,RMVar_hsa_circ_77218,RMVar_hsa_circ_253708 51133 RMVar_ID_51133 Human_SNP_ID_375635814 A-to-I Human chr8 - 102481345 102481345 102481345 CTGACACTTGTAGTCCCAGCTATCAAGAGGCTAAAGCAGGAGGATCCTGAGCCCAGGAGTTCAAG CTGACACTTGTAGTCCCAGCTATCAAGAGGCTTAAGCAGGAGGATCCTGAGCCCAGGAGTTCAAG T A - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1046514804 Functional Loss SNV dbSNP153 33..33 33 - - - 51134 RMVar_ID_51134 Human_SNP_ID_375722783 A-to-I Human chr8 - 102830361 102830361 102830361 GTCTCATTCTGTCACCCAGGCTGGAGTGCAGTAGCACAGCCTTGGCTCACTGTCTCACTGTCTTA GTCTCATTCTGTCACCCAGGCTGGAGTGCAGTGGCACAGCCTTGGCTCACTGTCTCACTGTCTTA T C AZIN1 Ensembl:ENSG00000155096 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1246991620 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12006,RMVar_hsa_circ_253717,RMVar_hsa_circ_253716,RMVar_hsa_circ_374327,RMVar_hsa_circ_346854,RMVar_hsa_circ_57983,RMVar_hsa_circ_253720,RMVar_hsa_circ_253719,RMVar_hsa_circ_346711,RMVar_hsa_circ_346749,RMVar_hsa_circ_70835,RMVar_hsa_circ_253721 51135 RMVar_ID_51135 Human_SNP_ID_375725205 A-to-I Human chr8 - 102839821 102839821 102839821 TATTTGTCTTTTTTTTTATAACCATAATAGACAGGGAAAAATGCATTTTTTGTGGGAGATCTTGG TATTTGTCTTTTTTTTTATAACCATAATAGACTGGGAAAAATGCATTTTTTGTGGGAGATCTTGG T A AZIN1 Ensembl:ENSG00000155096 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs758411643 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26189016 Human_Splice_Rec_998986,Human_Splice_Rec_999008,Human_Splice_Rec_999042,Human_Splice_Rec_999052 Human_miRNA_ID_343879,Human_miRNA_ID_1696180 RMVar_hsa_circ_253717,RMVar_hsa_circ_253716,RMVar_hsa_circ_374327,RMVar_hsa_circ_253722,RMVar_hsa_circ_71944,RMVar_hsa_circ_57983,RMVar_hsa_circ_253720,RMVar_hsa_circ_253719,RMVar_hsa_circ_346711,RMVar_hsa_circ_335862,RMVar_hsa_circ_253721,RMVar_hsa_circ_333854,RMVar_hsa_circ_291201,RMVar_hsa_circ_253723,RMVar_hsa_circ_253736,RMVar_hsa_circ_56739,RMVar_hsa_circ_253731,RMVar_hsa_circ_292255,RMVar_hsa_circ_301296,RMVar_hsa_circ_253732,RMVar_hsa_circ_326256,RMVar_hsa_circ_333034,RMVar_hsa_circ_275862,RMVar_hsa_circ_253734,RMVar_hsa_circ_299900,RMVar_hsa_circ_322747,RMVar_hsa_circ_285419,RMVar_hsa_circ_253738,RMVar_hsa_circ_124698,RMVar_hsa_circ_253737,RMVar_hsa_circ_27185,RMVar_hsa_circ_377862,RMVar_hsa_circ_253735,RMVar_hsa_circ_292537,RMVar_hsa_circ_253739 51136 RMVar_ID_51136 Human_SNP_ID_375728518 A-to-I Human chr8 - 102853439 102853439 102853439 AGAGTGCAGTGGCGCGATTTCAGCTCACTGCAAACTCCACCTCCCGGGTTCCATCAATTCTCCTG AGAGTGCAGTGGCGCGATTTCAGCTCACTGCAGACTCCACCTCCCGGGTTCCATCAATTCTCCTG T C AZIN1 Ensembl:ENSG00000155096 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1261916583 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16307253 RMVar_hsa_circ_253717,RMVar_hsa_circ_374327,RMVar_hsa_circ_71944,RMVar_hsa_circ_57983,RMVar_hsa_circ_253719,RMVar_hsa_circ_56739,RMVar_hsa_circ_299900,RMVar_hsa_circ_124698,RMVar_hsa_circ_253735,RMVar_hsa_circ_288571,RMVar_hsa_circ_253742,RMVar_hsa_circ_318159 51137 RMVar_ID_51137 Human_SNP_ID_375728655 A-to-I Human chr8 - 102854010 102854010 102854010 TTGAACCCGGGAGGCGGAGGTTGCAGTGAGCCAAGATGGTGCCACCGCACTGTAGACTAGGAGAC TTGAACCCGGGAGGCGGAGGTTGCAGTGAGCCGAGATGGTGCCACCGCACTGTAGACTAGGAGAC T C AZIN1 Ensembl:ENSG00000155096 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1276106066 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_253717,RMVar_hsa_circ_374327,RMVar_hsa_circ_71944,RMVar_hsa_circ_57983,RMVar_hsa_circ_253719,RMVar_hsa_circ_56739,RMVar_hsa_circ_299900,RMVar_hsa_circ_124698,RMVar_hsa_circ_253735,RMVar_hsa_circ_288571,RMVar_hsa_circ_253742,RMVar_hsa_circ_318159 51138 RMVar_ID_51138 Human_SNP_ID_375728985 A-to-I Human chr8 - 102855194 102855179 102855195 AAATTAGTCGAGCGTCGTGGCAGGTGCCTGTAATGCCAACTACTCGTGGGAGGCTGAGGCAGGAG AAATTAGTCGAGCGTCGTGGCAGGTGCCTGT________________GGGAGGCTGAGGCAGGAG CACGAGTAGTTGGCATT C AZIN1 Ensembl:ENSG00000155096 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1468834214 Functional Loss DEL dbSNP153 32..47 33 - - - RMVar_hsa_circ_253717,RMVar_hsa_circ_374327,RMVar_hsa_circ_71944,RMVar_hsa_circ_57983,RMVar_hsa_circ_253719,RMVar_hsa_circ_56739,RMVar_hsa_circ_299900,RMVar_hsa_circ_124698,RMVar_hsa_circ_253735,RMVar_hsa_circ_288571,RMVar_hsa_circ_253742,RMVar_hsa_circ_318159 51139 RMVar_ID_51139 Human_SNP_ID_375728988 A-to-I Human chr8 - 102855188 102855188 102855188 GTCGAGCGTCGTGGCAGGTGCCTGTAATGCCAACTACTCGTGGGAGGCTGAGGCAGGAGAATCAC GTCGAGCGTCGTGGCAGGTGCCTGTAATGCCAGCTACTCGTGGGAGGCTGAGGCAGGAGAATCAC T C AZIN1 Ensembl:ENSG00000155096 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs994635436 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_253717,RMVar_hsa_circ_374327,RMVar_hsa_circ_71944,RMVar_hsa_circ_57983,RMVar_hsa_circ_253719,RMVar_hsa_circ_56739,RMVar_hsa_circ_299900,RMVar_hsa_circ_124698,RMVar_hsa_circ_253735,RMVar_hsa_circ_288571,RMVar_hsa_circ_253742,RMVar_hsa_circ_318159 51140 RMVar_ID_51140 Human_SNP_ID_375737446 A-to-I Human chr8 + 102888659 102888659 102888659 CTCCTCAGCCAGGCCTGCTGGCTCACGTCTGTAATCCCAACACTTTGGGAGGCTGAGGCAGGTGA CTCCTCAGCCAGGCCTGCTGGCTCACGTCTGTGATCCCAACACTTTGGGAGGCTGAGGCAGGTGA A G AZIN1-AS1 Ensembl:ENSG00000253320 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1047057674 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_253746,RMVar_hsa_circ_253745 51141 RMVar_ID_51141 Human_SNP_ID_375738457 A-to-I Human chr8 + 102893047 102893047 102893047 TTTTGTAGAGATGGGGATTCCCTATGTTCCCCAGACTGGTCTCGAACTCCTGGGCTCAAGCTATC TTTTGTAGAGATGGGGATTCCCTATGTTCCCCGGACTGGTCTCGAACTCCTGGGCTCAAGCTATC A G AP003354.2,AZIN1-AS1 Ensembl:ENSG00000253263,Ensembl:ENSG00000253320 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946907813 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_253746,RMVar_hsa_circ_253745 51142 RMVar_ID_51142 Human_SNP_ID_375748952 A-to-I Human chr8 + 102936980 102936980 102936980 TTGTATTTTTAGTGGAGATGGGGTTTCACCATATTGGCCATCCTGGTCTCGAATTCCTGATCTCA TTGTATTTTTAGTGGAGATGGGGTTTCACCATGTTGGCCATCCTGGTCTCGAATTCCTGATCTCA A G AZIN1-AS1 Ensembl:ENSG00000253320 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs972491212 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_253746,RMVar_hsa_circ_253745 51143 RMVar_ID_51143 Human_SNP_ID_375780807 A-to-I Human chr8 + 103068795 103068795 103068795 CCGACAATCCTGTCCTTGTGTTTGTGTGTGCTAACAGAAATAAGTTGCAGTATGGTCGTACTTTT CCGACAATCCTGTCCTTGTGTTTGTGTGTGCTGACAGAAATAAGTTGCAGTATGGTCGTACTTTT A G ATP6V1C1 Ensembl:ENSG00000155097 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs777987893 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_692507,Human_RBP_ID_16308167,Human_RBP_ID_21563144,Human_RBP_ID_24239086,Human_RBP_ID_24518295 RMVar_hsa_circ_266994 51144 RMVar_ID_51144 Human_SNP_ID_375855804 A-to-I Human chr8 - 103394866 103394866 103394866 TATTATATTTTTAGTAAAAACAGGGTTTCACCATGTTGACCAGGCTGGTCTCGAACTCCTGACCT TATTATATTTTTAGTAAAAACAGGGTTTCACCGTGTTGACCAGGCTGGTCTCGAACTCCTGACCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1406454239 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_253757,RMVar_hsa_circ_253756 51145 RMVar_ID_51145 Human_SNP_ID_375858300 A-to-I Human chr8 - 103404353 103404353 103404353 TTGACCTCTTGATCCACCTGCCTCTGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCACG TTGACCTCTTGATCCACCTGCCTCTGCCTCCCGAAGTGCTGGGATTACAGGCATGAGCCACCACG T C AC012213.5,SLC25A32 Ensembl:ENSG00000285982,Ensembl:ENSG00000164933 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1455375474 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8676956 RMVar_hsa_circ_253757,RMVar_hsa_circ_253756,RMVar_hsa_circ_58724,RMVar_hsa_circ_253761,RMVar_hsa_circ_84751,RMVar_hsa_circ_253764,RMVar_hsa_circ_253763,RMVar_hsa_circ_253762,RMVar_hsa_circ_253765,RMVar_hsa_circ_253766,RMVar_hsa_circ_253768,RMVar_hsa_circ_275201,RMVar_hsa_circ_339520,RMVar_hsa_circ_253767 51146 RMVar_ID_51146 Human_SNP_ID_375878711 A-to-I Human chr8 - 103487586 103487586 103487586 CACCTCCTGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGTGCGTG CACCTCCTGGGTTCAAGCGATTCTCCTGCCTCGGCCTCCTGAGTAGCTGGGATTACAGGTGCGTG T C AC012213.5,AC012213.1 Ensembl:ENSG00000285982,Ensembl:ENSG00000253477 Protein coding,lincRNA intron,exon GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1240293071 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_999610,Human_Splice_Rec_999611 51147 RMVar_ID_51147 Human_SNP_ID_376007765 A-to-I Human chr8 + 103993845 103993845 103993845 GCCCAGGAGTTCTCAACCAGTCTAGGCCATATAGTGAGACCCTATCTCCACAAACACACACAAAA GCCCAGGAGTTCTCAACCAGTCTAGGCCATATGGTGAGACCCTATCTCCACAAACACACACAAAA A G RIMS2 Ensembl:ENSG00000176406 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1384889557 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25075,RMVar_hsa_circ_1279,RMVar_hsa_circ_50404,RMVar_hsa_circ_43887,RMVar_hsa_circ_27640,RMVar_hsa_circ_284231,RMVar_hsa_circ_320811,RMVar_hsa_circ_337859,RMVar_hsa_circ_289485,RMVar_hsa_circ_27737,RMVar_hsa_circ_9913,RMVar_hsa_circ_304473,RMVar_hsa_circ_314341,RMVar_hsa_circ_335908,RMVar_hsa_circ_344904,RMVar_hsa_circ_43077,RMVar_hsa_circ_253790,RMVar_hsa_circ_324961,RMVar_hsa_circ_320337,RMVar_hsa_circ_26201,RMVar_hsa_circ_14093,RMVar_hsa_circ_253802,RMVar_hsa_circ_2644,RMVar_hsa_circ_339317,RMVar_hsa_circ_349555,RMVar_hsa_circ_322785,RMVar_hsa_circ_331699,RMVar_hsa_circ_341996,RMVar_hsa_circ_327038,RMVar_hsa_circ_321349,RMVar_hsa_circ_278788,RMVar_hsa_circ_253800,RMVar_hsa_circ_253801,RMVar_hsa_circ_253799,RMVar_hsa_circ_50408,RMVar_hsa_circ_24233,RMVar_hsa_circ_253807,RMVar_hsa_circ_328512,RMVar_hsa_circ_344989,RMVar_hsa_circ_303524,RMVar_hsa_circ_253810 51148 RMVar_ID_51148 Human_SNP_ID_376014299 A-to-I Human chr8 + 104022481 104022481 104022481 CTCAGCTCACTGCAACCTCCCCCTCCCGGCTCAAGGGATTCTCCTGCCTCAGCCTTCTGAGTAGC CTCAGCTCACTGCAACCTCCCCCTCCCGGCTCTAGGGATTCTCCTGCCTCAGCCTTCTGAGTAGC A T RIMS2 Ensembl:ENSG00000176406 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1421123243 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25075,RMVar_hsa_circ_1279,RMVar_hsa_circ_43887,RMVar_hsa_circ_284231,RMVar_hsa_circ_289485,RMVar_hsa_circ_27737,RMVar_hsa_circ_314341,RMVar_hsa_circ_344904,RMVar_hsa_circ_26201,RMVar_hsa_circ_14093,RMVar_hsa_circ_2644,RMVar_hsa_circ_339317,RMVar_hsa_circ_322785,RMVar_hsa_circ_327038,RMVar_hsa_circ_321349,RMVar_hsa_circ_344989,RMVar_hsa_circ_49743,RMVar_hsa_circ_38416,RMVar_hsa_circ_286727,RMVar_hsa_circ_300781,RMVar_hsa_circ_275783,RMVar_hsa_circ_282022,RMVar_hsa_circ_253811 51149 RMVar_ID_51149 Human_SNP_ID_376067310 A-to-I Human chr8 + 104243514 104243514 104243514 CAAGACCAGCCTGGCCAACATAGCGAAACCCCATCTCTACTAAAAATACAAAAAATTAGAAGGGC CAAGACCAGCCTGGCCAACATAGCGAAACCCCGTCTCTACTAAAAATACAAAAAATTAGAAGGGC A G RIMS2 Ensembl:ENSG00000176406 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs186397000 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_49141,RMVar_hsa_circ_117582,RMVar_hsa_circ_253817 51150 RMVar_ID_51150 Human_SNP_ID_69935947 A-to-I Human chr2 - 45403896 45403896 45403896 TAAAATCATCAACAAAATTCAGAGTAAATATTAAAATAAGAGTACAAAGAATATGGGGAACACTG TAAAATCATCAACAAAATTCAGAGTAAATATTCAAATAAGAGTACAAAGAATATGGGGAACACTG T G SRBD1 Ensembl:ENSG00000068784 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs756223841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2647726 RMVar_hsa_circ_94450,RMVar_hsa_circ_122913,RMVar_hsa_circ_199496,RMVar_hsa_circ_199497 51151 RMVar_ID_51151 Human_SNP_ID_69979929 A-to-I Human chr2 - 45555203 45555203 45555203 ATTTTTATTTTTTGTAGAGACAAGGTCTGGCTATGTTGCCCAGACTAGTCTTGAACTCCAAGTGA ATTTTTATTTTTTGTAGAGACAAGGTCTGGCTGTGTTGCCCAGACTAGTCTTGAACTCCAAGTGA T C SRBD1 Ensembl:ENSG00000068784 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560648862 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89575,RMVar_hsa_circ_59457,RMVar_hsa_circ_122913,RMVar_hsa_circ_199496,RMVar_hsa_circ_368353,RMVar_hsa_circ_288394,RMVar_hsa_circ_305297,RMVar_hsa_circ_199504,RMVar_hsa_circ_66232,RMVar_hsa_circ_303338,RMVar_hsa_circ_199503,RMVar_hsa_circ_320480,RMVar_hsa_circ_199511,RMVar_hsa_circ_301849,RMVar_hsa_circ_199513,RMVar_hsa_circ_367808,RMVar_hsa_circ_344393,RMVar_hsa_circ_286538,RMVar_hsa_circ_283573,RMVar_hsa_circ_199517,RMVar_hsa_circ_81217,RMVar_hsa_circ_116639,RMVar_hsa_circ_121419,RMVar_hsa_circ_108652,RMVar_hsa_circ_199521,RMVar_hsa_circ_199522,RMVar_hsa_circ_199519,RMVar_hsa_circ_199520,RMVar_hsa_circ_199518,RMVar_hsa_circ_199515,RMVar_hsa_circ_199516,RMVar_hsa_circ_199526,RMVar_hsa_circ_370939,RMVar_hsa_circ_199514,RMVar_hsa_circ_269373,RMVar_hsa_circ_266155,RMVar_hsa_circ_268105,RMVar_hsa_circ_30750 51152 RMVar_ID_51152 Human_SNP_ID_69979960 A-to-I Human chr2 - 45555325 45555325 45555325 AGCTGTAGTGCAGTGGTGCATCATGGCTTACTACAGCTTCAACCTCCTGGGCTCAAGTGATCCTC AGCTGTAGTGCAGTGGTGCATCATGGCTTACTGCAGCTTCAACCTCCTGGGCTCAAGTGATCCTC T C SRBD1 Ensembl:ENSG00000068784 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs183232241 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89575,RMVar_hsa_circ_59457,RMVar_hsa_circ_122913,RMVar_hsa_circ_199496,RMVar_hsa_circ_368353,RMVar_hsa_circ_288394,RMVar_hsa_circ_305297,RMVar_hsa_circ_199504,RMVar_hsa_circ_66232,RMVar_hsa_circ_303338,RMVar_hsa_circ_199503,RMVar_hsa_circ_320480,RMVar_hsa_circ_199511,RMVar_hsa_circ_301849,RMVar_hsa_circ_199513,RMVar_hsa_circ_367808,RMVar_hsa_circ_344393,RMVar_hsa_circ_286538,RMVar_hsa_circ_283573,RMVar_hsa_circ_199517,RMVar_hsa_circ_81217,RMVar_hsa_circ_116639,RMVar_hsa_circ_121419,RMVar_hsa_circ_108652,RMVar_hsa_circ_199521,RMVar_hsa_circ_199522,RMVar_hsa_circ_199519,RMVar_hsa_circ_199520,RMVar_hsa_circ_199518,RMVar_hsa_circ_199515,RMVar_hsa_circ_199516,RMVar_hsa_circ_199526,RMVar_hsa_circ_370939,RMVar_hsa_circ_199514,RMVar_hsa_circ_269373,RMVar_hsa_circ_266155,RMVar_hsa_circ_268105,RMVar_hsa_circ_30750 51153 RMVar_ID_51153 Human_SNP_ID_69981389 A-to-I Human chr2 - 45559878 45559878 45559878 AGGGGTTTTGCCATATTTCCCAGGCTGTTCTCAAACTCCTGAACTCAAGTGATCCACCAACTTCC AGGGGTTTTGCCATATTTCCCAGGCTGTTCTCGAACTCCTGAACTCAAGTGATCCACCAACTTCC T C SRBD1 Ensembl:ENSG00000068784 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1241386986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13902072 RMVar_hsa_circ_89575,RMVar_hsa_circ_59457,RMVar_hsa_circ_122913,RMVar_hsa_circ_199496,RMVar_hsa_circ_368353,RMVar_hsa_circ_288394,RMVar_hsa_circ_305297,RMVar_hsa_circ_199504,RMVar_hsa_circ_66232,RMVar_hsa_circ_303338,RMVar_hsa_circ_199503,RMVar_hsa_circ_320480,RMVar_hsa_circ_199511,RMVar_hsa_circ_301849,RMVar_hsa_circ_199513,RMVar_hsa_circ_367808,RMVar_hsa_circ_344393,RMVar_hsa_circ_286538,RMVar_hsa_circ_283573,RMVar_hsa_circ_199517,RMVar_hsa_circ_81217,RMVar_hsa_circ_116639,RMVar_hsa_circ_121419,RMVar_hsa_circ_108652,RMVar_hsa_circ_199521,RMVar_hsa_circ_199522,RMVar_hsa_circ_199519,RMVar_hsa_circ_199520,RMVar_hsa_circ_199518,RMVar_hsa_circ_199515,RMVar_hsa_circ_199516,RMVar_hsa_circ_199526,RMVar_hsa_circ_370939,RMVar_hsa_circ_199514,RMVar_hsa_circ_269373,RMVar_hsa_circ_266155,RMVar_hsa_circ_268105,RMVar_hsa_circ_30750 51154 RMVar_ID_51154 Human_SNP_ID_70020307 A-to-I Human chr2 + 45692517 45692517 45692517 TCATCTGAACTTGATTACTCTGCAAAGGCCATATTTCCAAATCAGGTCACATTCATCAGTACCGA TCATCTGAACTTGATTACTCTGCAAAGGCCATTTTTCCAAATCAGGTCACATTCATCAGTACCGA A T PRKCE Ensembl:ENSG00000171132 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924281168 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 51155 RMVar_ID_51155 Human_SNP_ID_70069772 A-to-I Human chr2 + 45868759 45868759 45868759 AGGAGTTCAAGACCAGCCTGGCCAACATGGGGAAACCCCATCTCTACTAAAAATACAAAAAATAA AGGAGTTCAAGACCAGCCTGGCCAACATGGGGGAACCCCATCTCTACTAAAAATACAAAAAATAA A G PRKCE Ensembl:ENSG00000171132 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1333022583 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28332,RMVar_hsa_circ_27698 51156 RMVar_ID_51156 Human_SNP_ID_70069773 A-to-I Human chr2 + 45868766 45868766 45868766 CAAGACCAGCCTGGCCAACATGGGGAAACCCCATCTCTACTAAAAATACAAAAAATAAAATAAAA CAAGACCAGCCTGGCCAACATGGGGAAACCCCGTCTCTACTAAAAATACAAAAAATAAAATAAAA A G PRKCE Ensembl:ENSG00000171132 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1436995849 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_28332,RMVar_hsa_circ_27698 51157 RMVar_ID_51157 Human_SNP_ID_70123379 A-to-I Human chr2 + 46059087 46059086 46059087 ATGCCTGTAACGTGGCAAGACCGTGTCTCCACAAAAAAATTTAAAAATTAGCTGAGCTTTGTGGT ATGCCTGTAACGTGGCAAGACCGTGTCTCCAC_AAAAAATTTAAAAATTAGCTGAGCTTTGTGGT CA C PRKCE Ensembl:ENSG00000171132 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1558405495 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_28332,RMVar_hsa_circ_347641,RMVar_hsa_circ_315277,RMVar_hsa_circ_66014 51158 RMVar_ID_51158 Human_SNP_ID_70254730 A-to-I Human chr2 - 46522245 46522245 46522245 GAGTCTCCGTCTGTCGCCCAGGCTGGAGTGCAATGGCACGGTCTTGGTTCACTGCAACCTCGACC GAGTCTCCGTCTGTCGCCCAGGCTGGAGTGCAGTGGCACGGTCTTGGTTCACTGCAACCTCGACC T C ATP6V1E2 Ensembl:ENSG00000250565 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1327220040 Functional Loss SNV dbSNP153 33..33 33 - - - 51159 RMVar_ID_51159 Human_SNP_ID_70266331 A-to-I Human chr2 + 46563842 46563842 46563842 TCCTCTTTTTTTCTCTTTTTCTTAATGGAGACAGGGTCTCCCTATGTTGCCCAGGCTGGTCTCAA TCCTCTTTTTTTCTCTTTTTCTTAATGGAGACGGGGTCTCCCTATGTTGCCCAGGCTGGTCTCAA A G RHOQ Ensembl:ENSG00000119729 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1490567379 Functional Loss SNV dbSNP153 33..33 33 - - - 51160 RMVar_ID_51160 Human_SNP_ID_70269809 A-to-I Human chr2 + 46577469 46577469 46577469 TGGCCCAGGTTGGAGTGCAGTGACGGGATCTCAGCTCACTGCAAGCTCTGCCTCCCGTGTTCATG TGGCCCAGGTTGGAGTGCAGTGACGGGATCTCGGCTCACTGCAAGCTCTGCCTCCCGTGTTCATG A G RHOQ Ensembl:ENSG00000119729 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs957363450 Functional Loss SNV dbSNP153 33..33 33 - - - 51161 RMVar_ID_51161 Human_SNP_ID_70273336 A-to-I Human chr2 - 46592180 46592180 46592180 TAGGCGGTTTGTTTATTGTTTTTAAAAAAGACAGGTTCTCACTCTCTTGCCCAGGCTGTCCTCTA TAGGCGGTTTGTTTATTGTTTTTAAAAAAGACGGGTTCTCACTCTCTTGCCCAGGCTGTCCTCTA T C PIGF Ensembl:ENSG00000151665 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017109454 Functional Loss SNV dbSNP153 33..33 33 - - - 51162 RMVar_ID_51162 Human_SNP_ID_70273440 A-to-I Human chr2 - 46592585 46592584 46592586 TACCACCAACGATGTACCAATTTGTGTTTCACAGAGTTACATCCATATGGGAGAATAGTCTCCAG TACCACCAACGATGTACCAATTTGTGTTTCA__GAGTTACATCCATATGGGAGAATAGTCTCCAG CTG C PIGF Ensembl:ENSG00000151665 Protein coding intron GSE105773 Glioblastoma cells,U87MG - 29724793 RNA-Seq:(High) rs746521746 Functional Loss DEL dbSNP153 32..33 33 - - - RMVar_hsa_circ_199572,RMVar_hsa_circ_301100,RMVar_hsa_circ_369497,RMVar_hsa_circ_199573 51163 RMVar_ID_51163 Human_SNP_ID_70281193 A-to-I Human chr2 + 46619672 46619672 46619672 AAAGCTGAATGAAAATAAAGCTTTGACTTCAAAAAAAGCAAGGTGGGTAAGAGGATCCATCGATG AAAGCTGAATGAAAATAAAGCTTTGACTTCAAGAAAAGCAAGGTGGGTAAGAGGATCCATCGATG A G CRIPT Ensembl:ENSG00000119878 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1448579632 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_915455,Human_RBP_ID_27817057 Human_Splice_Rec_242180,Human_Splice_Rec_242181,Human_Splice_Rec_242188,Human_Splice_Rec_242189 RMVar_hsa_circ_102068,RMVar_hsa_circ_199575 51164 RMVar_ID_51164 Human_SNP_ID_70287857 A-to-I Human chr2 + 46641515 46641515 46641515 CCACACACTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGTGCCCAGCTGGACTTT CCACACACTTGGCCTCCCAAAGTGCTGGGATTTCAGGCGTGAGCCACTGTGCCCAGCTGGACTTT A T lnc-CRIPT-1 RNACentral:URS00008BA992 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1019955440 Functional Loss SNV dbSNP153 33..33 33 - - - 51165 RMVar_ID_51165 Human_SNP_ID_70287919 A-to-I Human chr2 + 46641763 46641763 46641763 GTCATGGACGGCAGGCGGAGTGTTTTGGGCCTATAATCCCAGCACTTTGGGAGGCTGATGCAGGA GTCATGGACGGCAGGCGGAGTGTTTTGGGCCTCTAATCCCAGCACTTTGGGAGGCTGATGCAGGA A C lnc-CRIPT-1 RNACentral:URS00008BA992 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs376343621 Functional Loss SNV dbSNP153 33..33 33 - - - 51166 RMVar_ID_51166 Human_SNP_ID_70288637 A-to-I Human chr2 + 46644285 46644285 46644285 TATAAAGAAAGGGGCTGGGCGCTGTGGCTCACACCTGTAATCCCAGCACTCTGGGAGGGCAAGGT TATAAAGAAAGGGGCTGGGCGCTGTGGCTCACGCCTGTAATCCCAGCACTCTGGGAGGGCAAGGT A G lnc-CRIPT-1 RNACentral:URS00008BA992 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs935638226 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25546706 51167 RMVar_ID_51167 Human_SNP_ID_70363790 A-to-I Human chr2 - 46910822 46910822 46910822 TTGTCTAGGCTGATCTCAAACTCCTGGCCTCAAGTGATCCTCCTGCCTCAGCCTCCCAAAGTGCT TTGTCTAGGCTGATCTCAAACTCCTGGCCTCAGGTGATCCTCCTGCCTCAGCCTCCCAAAGTGCT T C MCFD2 Ensembl:ENSG00000180398 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs769272477 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_242292,Human_Splice_Rec_242293,Human_Splice_Rec_242310,Human_Splice_Rec_242311 RMVar_hsa_circ_92537,RMVar_hsa_circ_199576,RMVar_hsa_circ_83123,RMVar_hsa_circ_199578 51168 RMVar_ID_51168 Human_SNP_ID_70379959 A-to-I Human chr2 + 46966955 46966955 46966955 ATTGTGTTGGCCGGGCGCGGTGGCTCATGCCTATAATCCCAGTACTTTGGGAGGCTGAGGCGGGT ATTGTGTTGGCCGGGCGCGGTGGCTCATGCCTGTAATCCCAGTACTTTGGGAGGCTGAGGCGGGT A G TTC7A Ensembl:ENSG00000068724 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs939963650 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_31106,RMVar_hsa_circ_308701,RMVar_hsa_circ_328204,RMVar_hsa_circ_35049,RMVar_hsa_circ_71095,RMVar_hsa_circ_34054,RMVar_hsa_circ_25697,RMVar_hsa_circ_199581,RMVar_hsa_circ_267327,RMVar_hsa_circ_278478 51169 RMVar_ID_51169 Human_SNP_ID_70413403 A-to-I Human chr2 - 47074485 47074485 47074485 GGCCGGTGCTCAGTACCCCTGGTCAGACCCCAAAGGCACTTGGTAGCAGGGGGAAAGAGCAAGGT GGCCGGTGCTCAGTACCCCTGGTCAGACCCCAGAGGCACTTGGTAGCAGGGGGAAAGAGCAAGGT T C STPG4,AC073283.3 Ensembl:ENSG00000239605,Ensembl:ENSG00000273269 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs10196117 Functional Loss SNV dbSNP153 33..33 33 - - - 51170 RMVar_ID_51170 Human_SNP_ID_70434492 A-to-I Human chr2 - 47139408 47139407 47139408 ACAGTACCTGCTCTCAAATTGAAAAAAAAAAAATAAAGCAGGAGAAGCTATATTAGTTTCAAACA ACAGTACCTGCTCTCAAATTGAAAAAAAAAAA_TAAAGCAGGAGAAGCTATATTAGTTTCAAACA AT A STPG4,AC073283.3 Ensembl:ENSG00000239605,Ensembl:ENSG00000273269 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs33970494 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_31639,RMVar_hsa_circ_312181 51171 RMVar_ID_51171 Human_SNP_ID_70443053 A-to-I Human chr2 - 47168621 47168621 47168621 GGTTCAAGCTGTTCTGCTTCAGTCTCCCGAGTAGCTGGGATTAGAGGCATGCACCACCTGGCTAT GGTTCAAGCTGTTCTGCTTCAGTCTCCCGAGTGGCTGGGATTAGAGGCATGCACCACCTGGCTAT T C CALM2,AC073283.3 Ensembl:ENSG00000143933,Ensembl:ENSG00000273269 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1252280357 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_36940,RMVar_hsa_circ_112100,RMVar_hsa_circ_58967,RMVar_hsa_circ_199599,RMVar_hsa_circ_312226 51172 RMVar_ID_51172 Human_SNP_ID_70443064 A-to-I Human chr2 - 47168647 47168647 47168647 TGCAGTGGCTCAACTTCTGTCTCCCGGGTTCAAGCTGTTCTGCTTCAGTCTCCCGAGTAGCTGGG TGCAGTGGCTCAACTTCTGTCTCCCGGGTTCAGGCTGTTCTGCTTCAGTCTCCCGAGTAGCTGGG T C CALM2,AC073283.3 Ensembl:ENSG00000143933,Ensembl:ENSG00000273269 Protein coding,Protein coding intron,intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs996093497 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13905736,Human_RBP_ID_17569582 RMVar_hsa_circ_36940,RMVar_hsa_circ_112100,RMVar_hsa_circ_58967,RMVar_hsa_circ_199599,RMVar_hsa_circ_312226 51173 RMVar_ID_51173 Human_SNP_ID_70443192 A-to-I Human chr2 - 47168997 47168997 47168997 GGCCGAGGCGGATCACTTGAGGTCAGGAGTTCATGACCAGCCTGGCCAACGTGGTGAAACCCCAT GGCCGAGGCGGATCACTTGAGGTCAGGAGTTCGTGACCAGCCTGGCCAACGTGGTGAAACCCCAT T C CALM2,AC073283.3 Ensembl:ENSG00000143933,Ensembl:ENSG00000273269 Protein coding,Protein coding intron,intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1558698677 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13905739 RMVar_hsa_circ_36940,RMVar_hsa_circ_112100,RMVar_hsa_circ_58967,RMVar_hsa_circ_199599,RMVar_hsa_circ_312226 51174 RMVar_ID_51174 Human_SNP_ID_70443194 A-to-I Human chr2 - 47169005 47169005 47169005 CTTTGGGAGGCCGAGGCGGATCACTTGAGGTCAGGAGTTCATGACCAGCCTGGCCAACGTGGTGA CTTTGGGAGGCCGAGGCGGATCACTTGAGGTCGGGAGTTCATGACCAGCCTGGCCAACGTGGTGA T C CALM2,AC073283.3 Ensembl:ENSG00000143933,Ensembl:ENSG00000273269 Protein coding,Protein coding intron,intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs917363568 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13905739 RMVar_hsa_circ_36940,RMVar_hsa_circ_112100,RMVar_hsa_circ_58967,RMVar_hsa_circ_199599,RMVar_hsa_circ_312226 51175 RMVar_ID_51175 Human_SNP_ID_70524824 A-to-I Human chr2 + 47422138 47422138 47422138 GACTAGCTAGTTTTTGTATTTTTTGCAGAGACAGGATTTCATCATGTTTTCTAGGCTGTTCTTGA GACTAGCTAGTTTTTGTATTTTTTGCAGAGACGGGATTTCATCATGTTTTCTAGGCTGTTCTTGA A G MSH2 Ensembl:ENSG00000095002 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1348659127 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17570379 RMVar_hsa_circ_19905,RMVar_hsa_circ_279965,RMVar_hsa_circ_293696,RMVar_hsa_circ_86773,RMVar_hsa_circ_199608,RMVar_hsa_circ_199609,RMVar_hsa_circ_199610,RMVar_hsa_circ_278482,RMVar_hsa_circ_4863,RMVar_hsa_circ_68439,RMVar_hsa_circ_342140,RMVar_hsa_circ_199613 51176 RMVar_ID_51176 Human_SNP_ID_70525001 A-to-I Human chr2 + 47422556 47422556 47422556 CCTGTGGTCCCAGTTACTTGGGAGGCTGAGGCAGGAGAATTGCTTGAACCTGGGAGGCAGAGGTT CCTGTGGTCCCAGTTACTTGGGAGGCTGAGGCGGGAGAATTGCTTGAACCTGGGAGGCAGAGGTT A G MSH2 Ensembl:ENSG00000095002 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1174993455 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19905,RMVar_hsa_circ_279965,RMVar_hsa_circ_293696,RMVar_hsa_circ_86773,RMVar_hsa_circ_199608,RMVar_hsa_circ_199609,RMVar_hsa_circ_199610,RMVar_hsa_circ_278482,RMVar_hsa_circ_4863,RMVar_hsa_circ_68439,RMVar_hsa_circ_342140,RMVar_hsa_circ_199613 51177 RMVar_ID_51177 Human_SNP_ID_70542895 A-to-I Human chr2 + 47469120 47469120 47469120 ACTACAGGTGTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGC ACTACAGGTGTTGCCCACTGCTTTGTATTTTTGATAGACACAGGATTTCCCCATGTTGCTCAGGC A G MSH2 Ensembl:ENSG00000095002 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886066006 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86773,RMVar_hsa_circ_199610,RMVar_hsa_circ_4863,RMVar_hsa_circ_324031,RMVar_hsa_circ_199616,RMVar_hsa_circ_337867,RMVar_hsa_circ_199614,RMVar_hsa_circ_298017,RMVar_hsa_circ_323927,RMVar_hsa_circ_199617,RMVar_hsa_circ_199618,RMVar_hsa_circ_340734 51178 RMVar_ID_51178 Human_SNP_ID_70542900 A-to-I Human chr2 + 47469129 47469129 47469129 GTTGCCCACTGCTTTGTATTTTTAATAGACACAGGATTTCCCCATGTTGCTCAGGCTGGTCTCGA GTTGCCCACTGCTTTGTATTTTTAATAGACACGGGATTTCCCCATGTTGCTCAGGCTGGTCTCGA A G MSH2 Ensembl:ENSG00000095002 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1050048040 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86773,RMVar_hsa_circ_199610,RMVar_hsa_circ_4863,RMVar_hsa_circ_324031,RMVar_hsa_circ_199616,RMVar_hsa_circ_337867,RMVar_hsa_circ_199614,RMVar_hsa_circ_298017,RMVar_hsa_circ_323927,RMVar_hsa_circ_199617,RMVar_hsa_circ_199618,RMVar_hsa_circ_340734 51179 RMVar_ID_51179 Human_SNP_ID_70642355 A-to-I Human chr2 + 47796840 47796840 47796840 AAAATTAGCTGGGCGTGGTGGCACACACCTGTAGTCCCAACCACTTGGGAGGCTGAGGCATGAGA AAAATTAGCTGGGCGTGGTGGCACACACCTGTGGTCCCAACCACTTGGGAGGCTGAGGCATGAGA A G MSH6 Ensembl:ENSG00000116062 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1010835607 Functional Loss SNV dbSNP153 33..33 33 - - - 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 51180 RMVar_ID_51180 Human_SNP_ID_70648751 A-to-I Human chr2 + 47806820 47806820 47806820 CCTGGCTAGTGAAAGGTCAACTGTAGATGCTGAAGCTGTCCATAAATTGCTGACTTTGATTAAGG CCTGGCTAGTGAAAGGTCAACTGTAGATGCTGCAGCTGTCCATAAATTGCTGACTTTGATTAAGG A C MSH6 Ensembl:ENSG00000116062 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1449733937 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_552006,Human_RBP_ID_1023495,Human_RBP_ID_1587598,Human_RBP_ID_1919140,Human_RBP_ID_3628018,Human_RBP_ID_6927920,Human_RBP_ID_8520681,Human_RBP_ID_8848674,Human_RBP_ID_9295946,Human_RBP_ID_13908369,Human_RBP_ID_17963943,Human_RBP_ID_18761988,Human_RBP_ID_23875087,Human_RBP_ID_25574841 Human_Splice_Rec_243316,Human_Splice_Rec_243332,Human_Splice_Rec_243348,Human_Splice_Rec_243364,Human_Splice_Rec_243388,Human_Splice_Rec_243412,Human_Splice_Rec_243428,Human_Splice_Rec_243456 Clinvar_Rec_140 RMVar_hsa_circ_84947,RMVar_hsa_circ_199625,RMVar_hsa_circ_109544,RMVar_hsa_circ_199630,RMVar_hsa_circ_100119,RMVar_hsa_circ_199631,RMVar_hsa_circ_95766,RMVar_hsa_circ_101186,RMVar_hsa_circ_101970,RMVar_hsa_circ_199632,RMVar_hsa_circ_199633,RMVar_hsa_circ_199634 51181 RMVar_ID_51181 Human_SNP_ID_70648798 A-to-I Human chr2 + 47806849 47806849 47806849 CTGAAGCTGTCCATAAATTGCTGACTTTGATTAAGGAATTATAGACTGACTACATTGGAAGCTTT CTGAAGCTGTCCATAAATTGCTGACTTTGATTGAGGAATTATAGACTGACTACATTGGAAGCTTT A G MSH6 Ensembl:ENSG00000116062 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs199739099 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_58293,Human_RBP_ID_552006,Human_RBP_ID_1587598,Human_RBP_ID_1919140,Human_RBP_ID_3628018,Human_RBP_ID_8520682,Human_RBP_ID_8848675,Human_RBP_ID_13908370,Human_RBP_ID_17699210,Human_RBP_ID_18761988,Human_RBP_ID_22993420,Human_RBP_ID_23875088 Human_Splice_Rec_243316,Human_Splice_Rec_243332,Human_Splice_Rec_243348,Human_Splice_Rec_243364,Human_Splice_Rec_243388,Human_Splice_Rec_243412,Human_Splice_Rec_243428,Human_Splice_Rec_243456 Clinvar_Rec_141 RMVar_hsa_circ_84947,RMVar_hsa_circ_199625,RMVar_hsa_circ_109544,RMVar_hsa_circ_199630,RMVar_hsa_circ_100119,RMVar_hsa_circ_199631,RMVar_hsa_circ_95766,RMVar_hsa_circ_101186,RMVar_hsa_circ_101970,RMVar_hsa_circ_199632,RMVar_hsa_circ_199633,RMVar_hsa_circ_199634 51182 RMVar_ID_51182 Human_SNP_ID_70651758 A-to-I Human chr2 - 47814580 47814580 47814580 GAGCCCAGGAGTTTGAGAACAGCCTGGGCAACATGGCAAAACTCCATCTCTACAAAAAATACAAA GAGCCCAGGAGTTTGAGAACAGCCTGGGCAACGTGGCAAAACTCCATCTCTACAAAAAATACAAA T C FBXO11 Ensembl:ENSG00000138081 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1403430896 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_17396,RMVar_hsa_circ_112677,RMVar_hsa_circ_199635,RMVar_hsa_circ_373607,RMVar_hsa_circ_329448,RMVar_hsa_circ_267809,RMVar_hsa_circ_199638,RMVar_hsa_circ_199639,RMVar_hsa_circ_87199,RMVar_hsa_circ_70580,RMVar_hsa_circ_199640,RMVar_hsa_circ_199641,RMVar_hsa_circ_35569,RMVar_hsa_circ_52782,RMVar_hsa_circ_23208,RMVar_hsa_circ_199642,RMVar_hsa_circ_17258,RMVar_hsa_circ_59623,RMVar_hsa_circ_90997,RMVar_hsa_circ_28359,RMVar_hsa_circ_199643 51183 RMVar_ID_51183 Human_SNP_ID_70654970 A-to-I Human chr2 - 47824376 47824376 47824376 ACAGTCCTCCCACCTCAGCCTCCCTAGTAACTAGGCTTATAGGCACATGTCACCACACCTGGCTA ACAGTCCTCCCACCTCAGCCTCCCTAGTAACTGGGCTTATAGGCACATGTCACCACACCTGGCTA T C FBXO11 Ensembl:ENSG00000138081 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs969701940 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5609,RMVar_hsa_circ_373607,RMVar_hsa_circ_329448,RMVar_hsa_circ_199638,RMVar_hsa_circ_199639,RMVar_hsa_circ_87199,RMVar_hsa_circ_70580,RMVar_hsa_circ_199640,RMVar_hsa_circ_35569,RMVar_hsa_circ_23208,RMVar_hsa_circ_90997,RMVar_hsa_circ_28359,RMVar_hsa_circ_199643,RMVar_hsa_circ_69323,RMVar_hsa_circ_51870,RMVar_hsa_circ_53104,RMVar_hsa_circ_123373,RMVar_hsa_circ_199649,RMVar_hsa_circ_342990,RMVar_hsa_circ_367723,RMVar_hsa_circ_373032,RMVar_hsa_circ_309849,RMVar_hsa_circ_270635,RMVar_hsa_circ_199647,RMVar_hsa_circ_199648,RMVar_hsa_circ_199650,RMVar_hsa_circ_199651 51184 RMVar_ID_51184 Human_SNP_ID_70656305 A-to-I Human chr2 - 47828120 47828120 47828120 TAAAAATTAGCTGGGCATGGTGGCACACGCCTATAATCCTAGCTACTTGGAAGGCTGAGGCAAGA TAAAAATTAGCTGGGCATGGTGGCACACGCCTGTAATCCTAGCTACTTGGAAGGCTGAGGCAAGA T C FBXO11 Ensembl:ENSG00000138081 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1415267730 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5609,RMVar_hsa_circ_373607,RMVar_hsa_circ_329448,RMVar_hsa_circ_199638,RMVar_hsa_circ_199639,RMVar_hsa_circ_87199,RMVar_hsa_circ_70580,RMVar_hsa_circ_199640,RMVar_hsa_circ_35569,RMVar_hsa_circ_23208,RMVar_hsa_circ_90997,RMVar_hsa_circ_28359,RMVar_hsa_circ_199643,RMVar_hsa_circ_69323,RMVar_hsa_circ_51870,RMVar_hsa_circ_53104,RMVar_hsa_circ_123373,RMVar_hsa_circ_199649,RMVar_hsa_circ_342990,RMVar_hsa_circ_367723,RMVar_hsa_circ_373032,RMVar_hsa_circ_309849,RMVar_hsa_circ_270635,RMVar_hsa_circ_199647,RMVar_hsa_circ_199648,RMVar_hsa_circ_199650,RMVar_hsa_circ_199651 51185 RMVar_ID_51185 Human_SNP_ID_70656452 A-to-I Human chr2 - 47828521 47828521 47828521 CACTGCAACCTCCACCTTCCAGGCTTCAAGCAATTCTTGTGTCTCAGTCTCCCGAGTAGGTGGGA CACTGCAACCTCCACCTTCCAGGCTTCAAGCAGTTCTTGTGTCTCAGTCTCCCGAGTAGGTGGGA T C FBXO11 Ensembl:ENSG00000138081 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs560571106 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5609,RMVar_hsa_circ_373607,RMVar_hsa_circ_329448,RMVar_hsa_circ_199638,RMVar_hsa_circ_199639,RMVar_hsa_circ_87199,RMVar_hsa_circ_70580,RMVar_hsa_circ_199640,RMVar_hsa_circ_35569,RMVar_hsa_circ_23208,RMVar_hsa_circ_90997,RMVar_hsa_circ_28359,RMVar_hsa_circ_199643,RMVar_hsa_circ_69323,RMVar_hsa_circ_51870,RMVar_hsa_circ_53104,RMVar_hsa_circ_123373,RMVar_hsa_circ_199649,RMVar_hsa_circ_342990,RMVar_hsa_circ_367723,RMVar_hsa_circ_373032,RMVar_hsa_circ_309849,RMVar_hsa_circ_270635,RMVar_hsa_circ_199647,RMVar_hsa_circ_199648,RMVar_hsa_circ_199650,RMVar_hsa_circ_199651 51186 RMVar_ID_51186 Human_SNP_ID_70656453 A-to-I Human chr2 - 47828521 47828521 47828521 CACTGCAACCTCCACCTTCCAGGCTTCAAGCAATTCTTGTGTCTCAGTCTCCCGAGTAGGTGGGA CACTGCAACCTCCACCTTCCAGGCTTCAAGCACTTCTTGTGTCTCAGTCTCCCGAGTAGGTGGGA T G FBXO11 Ensembl:ENSG00000138081 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs560571106 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5609,RMVar_hsa_circ_373607,RMVar_hsa_circ_329448,RMVar_hsa_circ_199638,RMVar_hsa_circ_199639,RMVar_hsa_circ_87199,RMVar_hsa_circ_70580,RMVar_hsa_circ_199640,RMVar_hsa_circ_35569,RMVar_hsa_circ_23208,RMVar_hsa_circ_90997,RMVar_hsa_circ_28359,RMVar_hsa_circ_199643,RMVar_hsa_circ_69323,RMVar_hsa_circ_51870,RMVar_hsa_circ_53104,RMVar_hsa_circ_123373,RMVar_hsa_circ_199649,RMVar_hsa_circ_342990,RMVar_hsa_circ_367723,RMVar_hsa_circ_373032,RMVar_hsa_circ_309849,RMVar_hsa_circ_270635,RMVar_hsa_circ_199647,RMVar_hsa_circ_199648,RMVar_hsa_circ_199650,RMVar_hsa_circ_199651 51187 RMVar_ID_51187 Human_SNP_ID_70656659 A-to-I Human chr2 - 47829046 47829046 47829046 GTGGTGGCGTGTGCCTGTAATCCCAGCCTCTCAGGAGGTTGAGGCATGAGAATCACTTGAAGTGG GTGGTGGCGTGTGCCTGTAATCCCAGCCTCTCGGGAGGTTGAGGCATGAGAATCACTTGAAGTGG T C FBXO11 Ensembl:ENSG00000138081 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1030725924 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5609,RMVar_hsa_circ_373607,RMVar_hsa_circ_329448,RMVar_hsa_circ_199638,RMVar_hsa_circ_199639,RMVar_hsa_circ_87199,RMVar_hsa_circ_70580,RMVar_hsa_circ_199640,RMVar_hsa_circ_35569,RMVar_hsa_circ_23208,RMVar_hsa_circ_90997,RMVar_hsa_circ_28359,RMVar_hsa_circ_199643,RMVar_hsa_circ_69323,RMVar_hsa_circ_51870,RMVar_hsa_circ_53104,RMVar_hsa_circ_123373,RMVar_hsa_circ_199649,RMVar_hsa_circ_342990,RMVar_hsa_circ_367723,RMVar_hsa_circ_373032,RMVar_hsa_circ_309849,RMVar_hsa_circ_270635,RMVar_hsa_circ_199647,RMVar_hsa_circ_199648,RMVar_hsa_circ_199650,RMVar_hsa_circ_199651 51188 RMVar_ID_51188 Human_SNP_ID_70656808 A-to-I Human chr2 - 47829420 47829420 47829420 CCTGGCCAACATGGTGAAACCCTGTCTCTACTAGAAATACATAAATTAGCCGGGTGTGTTGGTGC CCTGGCCAACATGGTGAAACCCTGTCTCTACTGGAAATACATAAATTAGCCGGGTGTGTTGGTGC T C FBXO11 Ensembl:ENSG00000138081 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs544991786 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5609,RMVar_hsa_circ_373607,RMVar_hsa_circ_329448,RMVar_hsa_circ_199638,RMVar_hsa_circ_199639,RMVar_hsa_circ_87199,RMVar_hsa_circ_70580,RMVar_hsa_circ_199640,RMVar_hsa_circ_35569,RMVar_hsa_circ_23208,RMVar_hsa_circ_90997,RMVar_hsa_circ_28359,RMVar_hsa_circ_199643,RMVar_hsa_circ_69323,RMVar_hsa_circ_51870,RMVar_hsa_circ_53104,RMVar_hsa_circ_123373,RMVar_hsa_circ_199649,RMVar_hsa_circ_342990,RMVar_hsa_circ_367723,RMVar_hsa_circ_373032,RMVar_hsa_circ_309849,RMVar_hsa_circ_270635,RMVar_hsa_circ_199647,RMVar_hsa_circ_199648,RMVar_hsa_circ_199650,RMVar_hsa_circ_199651 51189 RMVar_ID_51189 Human_SNP_ID_70657445 A-to-I Human chr2 - 47831323 47831323 47831323 GCAACCTCCACCTCCTGGTTCAAGCGATTCTCATGTCTCAGCCTTCCAAGTAGCTGGGATTACAG GCAACCTCCACCTCCTGGTTCAAGCGATTCTCGTGTCTCAGCCTTCCAAGTAGCTGGGATTACAG T C FBXO11 Ensembl:ENSG00000138081 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1010051107 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5609,RMVar_hsa_circ_373607,RMVar_hsa_circ_329448,RMVar_hsa_circ_199638,RMVar_hsa_circ_199639,RMVar_hsa_circ_87199,RMVar_hsa_circ_70580,RMVar_hsa_circ_199640,RMVar_hsa_circ_35569,RMVar_hsa_circ_23208,RMVar_hsa_circ_90997,RMVar_hsa_circ_28359,RMVar_hsa_circ_199643,RMVar_hsa_circ_69323,RMVar_hsa_circ_51870,RMVar_hsa_circ_53104,RMVar_hsa_circ_123373,RMVar_hsa_circ_199649,RMVar_hsa_circ_342990,RMVar_hsa_circ_367723,RMVar_hsa_circ_373032,RMVar_hsa_circ_309849,RMVar_hsa_circ_270635,RMVar_hsa_circ_199647,RMVar_hsa_circ_199648,RMVar_hsa_circ_199650,RMVar_hsa_circ_199651 51190 RMVar_ID_51190 Human_SNP_ID_70659572 A-to-I Human chr2 - 47837480 47837480 47837480 TCTTGTTGCCCAGGCTAGAGTGCAGTGGCACAATCTTGACTCACTGCAACCTCTGCCTCCCGGGT TCTTGTTGCCCAGGCTAGAGTGCAGTGGCACAGTCTTGACTCACTGCAACCTCTGCCTCCCGGGT T C FBXO11 Ensembl:ENSG00000138081 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs926526384 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_373607,RMVar_hsa_circ_199639,RMVar_hsa_circ_23208,RMVar_hsa_circ_90997,RMVar_hsa_circ_199643,RMVar_hsa_circ_199652,RMVar_hsa_circ_123373,RMVar_hsa_circ_199649,RMVar_hsa_circ_373032,RMVar_hsa_circ_199650,RMVar_hsa_circ_199651,RMVar_hsa_circ_365311,RMVar_hsa_circ_281285,RMVar_hsa_circ_349242,RMVar_hsa_circ_199661,RMVar_hsa_circ_312521,RMVar_hsa_circ_199667,RMVar_hsa_circ_97443,RMVar_hsa_circ_367958,RMVar_hsa_circ_199663,RMVar_hsa_circ_199668,RMVar_hsa_circ_199669,RMVar_hsa_circ_311162 51191 RMVar_ID_51191 Human_SNP_ID_70659573 A-to-I Human chr2 - 47837481 47837481 47837481 TTCTTGTTGCCCAGGCTAGAGTGCAGTGGCACAATCTTGACTCACTGCAACCTCTGCCTCCCGGG TTCTTGTTGCCCAGGCTAGAGTGCAGTGGCACCATCTTGACTCACTGCAACCTCTGCCTCCCGGG T G FBXO11 Ensembl:ENSG00000138081 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1474088082 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_373607,RMVar_hsa_circ_199639,RMVar_hsa_circ_23208,RMVar_hsa_circ_90997,RMVar_hsa_circ_199643,RMVar_hsa_circ_199652,RMVar_hsa_circ_123373,RMVar_hsa_circ_199649,RMVar_hsa_circ_373032,RMVar_hsa_circ_199650,RMVar_hsa_circ_199651,RMVar_hsa_circ_365311,RMVar_hsa_circ_281285,RMVar_hsa_circ_349242,RMVar_hsa_circ_199661,RMVar_hsa_circ_312521,RMVar_hsa_circ_199667,RMVar_hsa_circ_97443,RMVar_hsa_circ_367958,RMVar_hsa_circ_199663,RMVar_hsa_circ_199668,RMVar_hsa_circ_199669,RMVar_hsa_circ_311162 51192 RMVar_ID_51192 Human_SNP_ID_70659575 A-to-I Human chr2 - 47837496 47837489 47837497 TTTGACGGAGTTTCGTTCTTGTTGCCCAGGCTAGAGTGCAGTGGCACAATCTTGACTCACTGCAA TTTGACGGAGTTTCGTTCTTGTTGCCCAGGC________AGTGGCACAATCTTGACTCACTGCAA TGCACTCTA T FBXO11 Ensembl:ENSG00000138081 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1412215513 Functional Loss DEL dbSNP153 32..39 33 - - - RMVar_hsa_circ_373607,RMVar_hsa_circ_199639,RMVar_hsa_circ_23208,RMVar_hsa_circ_90997,RMVar_hsa_circ_199643,RMVar_hsa_circ_199652,RMVar_hsa_circ_123373,RMVar_hsa_circ_199649,RMVar_hsa_circ_373032,RMVar_hsa_circ_199650,RMVar_hsa_circ_199651,RMVar_hsa_circ_365311,RMVar_hsa_circ_281285,RMVar_hsa_circ_349242,RMVar_hsa_circ_199661,RMVar_hsa_circ_312521,RMVar_hsa_circ_199667,RMVar_hsa_circ_97443,RMVar_hsa_circ_367958,RMVar_hsa_circ_199663,RMVar_hsa_circ_199668,RMVar_hsa_circ_199669,RMVar_hsa_circ_311162 51193 RMVar_ID_51193 Human_SNP_ID_70667109 A-to-I Human chr2 - 47858982 47858982 47858982 GGCTGGAGTGCAGAGTGGCGCGATCTCTGCTCACTGCGACCTCCGCCTCCCGGATTCAAGCCATT GGCTGGAGTGCAGAGTGGCGCGATCTCTGCTCTCTGCGACCTCCGCCTCCCGGATTCAAGCCATT T A FBXO11 Ensembl:ENSG00000138081 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223049962 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13908738 51194 RMVar_ID_51194 Human_SNP_ID_70667110 A-to-I Human chr2 - 47858982 47858982 47858982 GGCTGGAGTGCAGAGTGGCGCGATCTCTGCTCACTGCGACCTCCGCCTCCCGGATTCAAGCCATT GGCTGGAGTGCAGAGTGGCGCGATCTCTGCTCGCTGCGACCTCCGCCTCCCGGATTCAAGCCATT T C FBXO11 Ensembl:ENSG00000138081 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1223049962 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13908738 51195 RMVar_ID_51195 Human_SNP_ID_70672136 A-to-I Human chr2 - 47874090 47874090 47874090 CCTGCCTCAGCCTCCCAAGTAGCTGGAATTACAGGTGCCCGCCACCATAGTCGGCTAATTTTTTG CCTGCCTCAGCCTCCCAAGTAGCTGGAATTACGGGTGCCCGCCACCATAGTCGGCTAATTTTTTG T C FBXO11 Ensembl:ENSG00000138081 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1291549109 Functional Loss SNV dbSNP153 33..33 33 - - - 51196 RMVar_ID_51196 Human_SNP_ID_70672158 A-to-I Human chr2 - 47874151 47874151 47874151 GGAGTGCAGTGGTGCAATCTCTGCTCACAGCAAGCTCCGCCTCCCAGGTTCAAGCGATTCTCCTG GGAGTGCAGTGGTGCAATCTCTGCTCACAGCAGGCTCCGCCTCCCAGGTTCAAGCGATTCTCCTG T C FBXO11 Ensembl:ENSG00000138081 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1362123707 Functional Loss SNV dbSNP153 33..33 33 - - - 51197 RMVar_ID_51197 Human_SNP_ID_70672161 A-to-I Human chr2 - 47874167 47874167 47874167 CACTATCGTCCGGACTGGAGTGCAGTGGTGCAATCTCTGCTCACAGCAAGCTCCGCCTCCCAGGT CACTATCGTCCGGACTGGAGTGCAGTGGTGCAGTCTCTGCTCACAGCAAGCTCCGCCTCCCAGGT T C FBXO11 Ensembl:ENSG00000138081 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs902864161 Functional Loss SNV dbSNP153 33..33 33 - - - 51198 RMVar_ID_51198 Human_SNP_ID_70672162 A-to-I Human chr2 - 47874167 47874167 47874167 CACTATCGTCCGGACTGGAGTGCAGTGGTGCAATCTCTGCTCACAGCAAGCTCCGCCTCCCAGGT CACTATCGTCCGGACTGGAGTGCAGTGGTGCACTCTCTGCTCACAGCAAGCTCCGCCTCCCAGGT T G FBXO11 Ensembl:ENSG00000138081 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs902864161 Functional Loss SNV dbSNP153 33..33 33 - - - 51199 RMVar_ID_51199 Human_SNP_ID_70672169 A-to-I Human chr2 - 47874176 47874176 47874176 ACAGTCTCGCACTATCGTCCGGACTGGAGTGCAGTGGTGCAATCTCTGCTCACAGCAAGCTCCGC ACAGTCTCGCACTATCGTCCGGACTGGAGTGCCGTGGTGCAATCTCTGCTCACAGCAAGCTCCGC T G FBXO11 Ensembl:ENSG00000138081 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1184228827 Functional Loss SNV dbSNP153 33..33 33 - - - 51200 RMVar_ID_51200 Human_SNP_ID_70672178 A-to-I Human chr2 - 47874195 47874195 47874195 TTTATTATTTATTTTTGAGACAGTCTCGCACTATCGTCCGGACTGGAGTGCAGTGGTGCAATCTC TTTATTATTTATTTTTGAGACAGTCTCGCACTGTCGTCCGGACTGGAGTGCAGTGGTGCAATCTC T C FBXO11 Ensembl:ENSG00000138081 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs368713054 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6928073 51201 RMVar_ID_51201 Human_SNP_ID_70674495 A-to-I Human chr2 - 47881104 47881104 47881104 GGGACTGCAGGCACCCGCCACTAAGCCCGGCTAATTTTTGTATTTTTAGTAGAGACGGGTTTCAC GGGACTGCAGGCACCCGCCACTAAGCCCGGCTGATTTTTGTATTTTTAGTAGAGACGGGTTTCAC T C FBXO11 Ensembl:ENSG00000138081 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1558468952 Functional Loss SNV dbSNP153 33..33 33 - - - 51202 RMVar_ID_51202 Human_SNP_ID_70680048 A-to-I Human chr2 - 47897440 47897440 47897440 TGCCCGCCTAAGCCTCCCAAAATGCTGGGATTACAGGCGTGAGCCACCTCACCCGACCAGAAGTT TGCCCGCCTAAGCCTCCCAAAATGCTGGGATTGCAGGCGTGAGCCACCTCACCCGACCAGAAGTT T C FBXO11 Ensembl:ENSG00000138081 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs537989982 Functional Loss SNV dbSNP153 33..33 33 - - - 51203 RMVar_ID_51203 Human_SNP_ID_70796309 A-to-I Human chr2 + 48317278 48317278 48317278 TGAGACCAGCCTGGCCAACGTGGCAAAACCCCATCTCTACCAAAAATACAAAAATTAGCTGGGCC TGAGACCAGCCTGGCCAACGTGGCAAAACCCCGTCTCTACCAAAAATACAAAAATTAGCTGGGCC A G FOXN2 Ensembl:ENSG00000170802 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs986731578 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89574,RMVar_hsa_circ_199676 51204 RMVar_ID_51204 Human_SNP_ID_70797888 A-to-I Human chr2 + 48322042 48322042 48322042 GTGATCTCGGCTTATTGCAATCTCCGCCTTCGAGGTTCAAGCAATTCTTTCTCAGCCCCTGGAGT GTGATCTCGGCTTATTGCAATCTCCGCCTTCGCGGTTCAAGCAATTCTTTCTCAGCCCCTGGAGT A C FOXN2 Ensembl:ENSG00000170802 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1266771940 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89574,RMVar_hsa_circ_199676 51205 RMVar_ID_51205 Human_SNP_ID_70797893 A-to-I Human chr2 + 48322048 48322048 48322048 TCGGCTTATTGCAATCTCCGCCTTCGAGGTTCAAGCAATTCTTTCTCAGCCCCTGGAGTAGCTGG TCGGCTTATTGCAATCTCCGCCTTCGAGGTTCCAGCAATTCTTTCTCAGCCCCTGGAGTAGCTGG A C FOXN2 Ensembl:ENSG00000170802 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1333768644 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89574,RMVar_hsa_circ_199676 51206 RMVar_ID_51206 Human_SNP_ID_70808169 A-to-I Human chr2 + 48357704 48357704 48357704 AGCAATCACCTTCGCCGGCTTCCCAAAGTGCTAGGATTACAGACGTGAGCCACCGCACCTGGCCT AGCAATCACCTTCGCCGGCTTCCCAAAGTGCTGGGATTACAGACGTGAGCCACCGCACCTGGCCT A G FOXN2 Ensembl:ENSG00000170802 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs561140287 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_89574,RMVar_hsa_circ_199682,RMVar_hsa_circ_290989,RMVar_hsa_circ_199676,RMVar_hsa_circ_356851,RMVar_hsa_circ_290486,RMVar_hsa_circ_93064,RMVar_hsa_circ_199683,RMVar_hsa_circ_199680,RMVar_hsa_circ_199681,RMVar_hsa_circ_199685,RMVar_hsa_circ_302844,RMVar_hsa_circ_319590 51207 RMVar_ID_51207 Human_SNP_ID_70846407 A-to-I Human chr2 + 48484068 48484068 48484068 TCAAAACAAACTTTGACGCCATAACAAAAATCATAGGCTGTGACTCCTGTAGCCACCCACACATT TCAAAACAAACTTTGACGCCATAACAAAAATCGTAGGCTGTGACTCCTGTAGCCACCCACACATT A G PPP1R21 Ensembl:ENSG00000162869 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1422498662 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_328020,RMVar_hsa_circ_284081,RMVar_hsa_circ_281781,RMVar_hsa_circ_30179,RMVar_hsa_circ_44269,RMVar_hsa_circ_73510,RMVar_hsa_circ_199694,RMVar_hsa_circ_199695,RMVar_hsa_circ_57601,RMVar_hsa_circ_32365,RMVar_hsa_circ_51467,RMVar_hsa_circ_68225,RMVar_hsa_circ_368582,RMVar_hsa_circ_266661,RMVar_hsa_circ_341793,RMVar_hsa_circ_287366,RMVar_hsa_circ_199705,RMVar_hsa_circ_199706,RMVar_hsa_circ_199714,RMVar_hsa_circ_301505,RMVar_hsa_circ_314976,RMVar_hsa_circ_320381,RMVar_hsa_circ_334042,RMVar_hsa_circ_373127,RMVar_hsa_circ_308622,RMVar_hsa_circ_82826,RMVar_hsa_circ_272373,RMVar_hsa_circ_199710,RMVar_hsa_circ_199712,RMVar_hsa_circ_199713,RMVar_hsa_circ_199711,RMVar_hsa_circ_199708,RMVar_hsa_circ_199709,RMVar_hsa_circ_378191,RMVar_hsa_circ_199707,RMVar_hsa_circ_199716,RMVar_hsa_circ_199717,RMVar_hsa_circ_305788,RMVar_hsa_circ_326917,RMVar_hsa_circ_361194,RMVar_hsa_circ_199718 51208 RMVar_ID_51208 Human_SNP_ID_70847958 A-to-I Human chr2 + 48488577 48488577 48488577 TATTTTTAGTAGAGACGGGATTTCACCATGTTAGTCAGGATGGTCTCAATCTCCTGAGAACTCTG TATTTTTAGTAGAGACGGGATTTCACCATGTTGGTCAGGATGGTCTCAATCTCCTGAGAACTCTG A G PPP1R21 Ensembl:ENSG00000162869 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1183023324 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_328020,RMVar_hsa_circ_284081,RMVar_hsa_circ_281781,RMVar_hsa_circ_30179,RMVar_hsa_circ_199694,RMVar_hsa_circ_199695,RMVar_hsa_circ_57601,RMVar_hsa_circ_32365,RMVar_hsa_circ_51467,RMVar_hsa_circ_68225,RMVar_hsa_circ_368582,RMVar_hsa_circ_266661,RMVar_hsa_circ_287366,RMVar_hsa_circ_199706,RMVar_hsa_circ_301505,RMVar_hsa_circ_314976,RMVar_hsa_circ_320381,RMVar_hsa_circ_334042,RMVar_hsa_circ_373127,RMVar_hsa_circ_82826,RMVar_hsa_circ_272373,RMVar_hsa_circ_199710,RMVar_hsa_circ_199712,RMVar_hsa_circ_199713,RMVar_hsa_circ_199711,RMVar_hsa_circ_199708,RMVar_hsa_circ_199709,RMVar_hsa_circ_378191,RMVar_hsa_circ_199707,RMVar_hsa_circ_199716,RMVar_hsa_circ_199717,RMVar_hsa_circ_305788,RMVar_hsa_circ_326917,RMVar_hsa_circ_361194,RMVar_hsa_circ_199718,RMVar_hsa_circ_64014,RMVar_hsa_circ_199719 51209 RMVar_ID_51209 Human_SNP_ID_70849638 A-to-I Human chr2 + 48494040 48494040 48494040 GTCCAGGAGTTCGAGATCAGCCTGGGCAACATAGGGAGACCTCGTCTCTCCAAAAAAAAAAAAAA GTCCAGGAGTTCGAGATCAGCCTGGGCAACATGGGGAGACCTCGTCTCTCCAAAAAAAAAAAAAA A G PPP1R21 Ensembl:ENSG00000162869 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1489051264 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25589602 RMVar_hsa_circ_328020,RMVar_hsa_circ_281781,RMVar_hsa_circ_30179,RMVar_hsa_circ_199695,RMVar_hsa_circ_68225,RMVar_hsa_circ_368582,RMVar_hsa_circ_266661,RMVar_hsa_circ_301505,RMVar_hsa_circ_314976,RMVar_hsa_circ_320381,RMVar_hsa_circ_334042,RMVar_hsa_circ_373127,RMVar_hsa_circ_82826,RMVar_hsa_circ_199710,RMVar_hsa_circ_199712,RMVar_hsa_circ_199711,RMVar_hsa_circ_199708,RMVar_hsa_circ_199709,RMVar_hsa_circ_199707,RMVar_hsa_circ_28917,RMVar_hsa_circ_305788,RMVar_hsa_circ_326917,RMVar_hsa_circ_199718 51210 RMVar_ID_51210 Human_SNP_ID_70853649 A-to-I Human chr2 + 48506100 48506092 48506100 ATTTTGAAATATTCTAAGATGTAACTTTATTTATTTATTTATTTAGAGACAGAGTCTCATTATAT ATTTTGAAATATTCTAAGATGTAAC________TTTATTTATTTAGAGACAGAGTCTCATTATAT CTTTATTTA C PPP1R21 Ensembl:ENSG00000162869 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs764136068 Functional Loss DEL dbSNP153 26..33 33 - - - Human_RBP_ID_13909873 RMVar_hsa_circ_199723,RMVar_hsa_circ_281781,RMVar_hsa_circ_30179,RMVar_hsa_circ_199695,RMVar_hsa_circ_266661,RMVar_hsa_circ_320381,RMVar_hsa_circ_334042,RMVar_hsa_circ_373127,RMVar_hsa_circ_82826,RMVar_hsa_circ_199710,RMVar_hsa_circ_199708,RMVar_hsa_circ_199709,RMVar_hsa_circ_199707,RMVar_hsa_circ_28917,RMVar_hsa_circ_326917,RMVar_hsa_circ_288606,RMVar_hsa_circ_199720,RMVar_hsa_circ_320952,RMVar_hsa_circ_199721,RMVar_hsa_circ_351816,RMVar_hsa_circ_294608,RMVar_hsa_circ_199725,RMVar_hsa_circ_199724,RMVar_hsa_circ_199722 51211 RMVar_ID_51211 Human_SNP_ID_70853650 A-to-I Human chr2 + 48506100 48506092 48506100 ATTTTGAAATATTCTAAGATGTAACTTTATTTATTTATTTATTTAGAGACAGAGTCTCATTATAT ATTTTGAAATATTCTAAGATGTAACTTTA____TTTATTTATTTAGAGACAGAGTCTCATTATAT CTTTATTTA CTTTA PPP1R21 Ensembl:ENSG00000162869 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs764136068 Functional Loss DEL dbSNP153 30..33 33 - - - Human_RBP_ID_13909873 RMVar_hsa_circ_199723,RMVar_hsa_circ_281781,RMVar_hsa_circ_30179,RMVar_hsa_circ_199695,RMVar_hsa_circ_266661,RMVar_hsa_circ_320381,RMVar_hsa_circ_334042,RMVar_hsa_circ_373127,RMVar_hsa_circ_82826,RMVar_hsa_circ_199710,RMVar_hsa_circ_199708,RMVar_hsa_circ_199709,RMVar_hsa_circ_199707,RMVar_hsa_circ_28917,RMVar_hsa_circ_326917,RMVar_hsa_circ_288606,RMVar_hsa_circ_199720,RMVar_hsa_circ_320952,RMVar_hsa_circ_199721,RMVar_hsa_circ_351816,RMVar_hsa_circ_294608,RMVar_hsa_circ_199725,RMVar_hsa_circ_199724,RMVar_hsa_circ_199722 51212 RMVar_ID_51212 Human_SNP_ID_70853653 A-to-I Human chr2 + 48506100 48506100 48506100 ATTTTGAAATATTCTAAGATGTAACTTTATTTATTTATTTATTTAGAGACAGAGTCTCATTATAT ATTTTGAAATATTCTAAGATGTAACTTTATTTTTTTATTTATTTAGAGACAGAGTCTCATTATAT A T PPP1R21 Ensembl:ENSG00000162869 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1006446490 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13909873 RMVar_hsa_circ_199723,RMVar_hsa_circ_281781,RMVar_hsa_circ_30179,RMVar_hsa_circ_199695,RMVar_hsa_circ_266661,RMVar_hsa_circ_320381,RMVar_hsa_circ_334042,RMVar_hsa_circ_373127,RMVar_hsa_circ_82826,RMVar_hsa_circ_199710,RMVar_hsa_circ_199708,RMVar_hsa_circ_199709,RMVar_hsa_circ_199707,RMVar_hsa_circ_28917,RMVar_hsa_circ_326917,RMVar_hsa_circ_288606,RMVar_hsa_circ_199720,RMVar_hsa_circ_320952,RMVar_hsa_circ_199721,RMVar_hsa_circ_351816,RMVar_hsa_circ_294608,RMVar_hsa_circ_199725,RMVar_hsa_circ_199724,RMVar_hsa_circ_199722 51213 RMVar_ID_51213 Human_SNP_ID_70853681 A-to-I Human chr2 + 48506191 48506191 48506191 ATCTCAGCTTACTGCAACCTCTGCCTCCGGGTACAAGTTATTCTCCTGCCTGAGCCTCGCAGGTA ATCTCAGCTTACTGCAACCTCTGCCTCCGGGTGCAAGTTATTCTCCTGCCTGAGCCTCGCAGGTA A G PPP1R21 Ensembl:ENSG00000162869 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1344731114 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_199723,RMVar_hsa_circ_281781,RMVar_hsa_circ_30179,RMVar_hsa_circ_199695,RMVar_hsa_circ_266661,RMVar_hsa_circ_320381,RMVar_hsa_circ_334042,RMVar_hsa_circ_373127,RMVar_hsa_circ_82826,RMVar_hsa_circ_199710,RMVar_hsa_circ_199708,RMVar_hsa_circ_199709,RMVar_hsa_circ_199707,RMVar_hsa_circ_28917,RMVar_hsa_circ_326917,RMVar_hsa_circ_288606,RMVar_hsa_circ_199720,RMVar_hsa_circ_320952,RMVar_hsa_circ_199721,RMVar_hsa_circ_351816,RMVar_hsa_circ_294608,RMVar_hsa_circ_199725,RMVar_hsa_circ_199724,RMVar_hsa_circ_199722 51214 RMVar_ID_51214 Human_SNP_ID_70883700 A-to-I Human chr2 + 48598951 48598951 48598951 AAAATTAGTTGGGCGTGGTGGCGGGCGCCTATAGTCCCAGCTACTGGGGAGGCTGAGGCAGGAGA AAAATTAGTTGGGCGTGGTGGCGGGCGCCTATGGTCCCAGCTACTGGGGAGGCTGAGGCAGGAGA A G STON1-GTF2A1L Ensembl:ENSG00000068781 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1164854045 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26761,RMVar_hsa_circ_199728 51215 RMVar_ID_51215 Human_SNP_ID_70885386 A-to-I Human chr2 + 48604207 48604207 48604207 ACCTCAGGCGATCCACCCACCTCTGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCAGTACAC ACCTCAGGCGATCCACCCACCTCTGCCTCCCAGAGTGCTGGGATTACAGGCATGAGCCAGTACAC A G STON1-GTF2A1L Ensembl:ENSG00000068781 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1194960694 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26761 51216 RMVar_ID_51216 Human_SNP_ID_70885387 A-to-I Human chr2 + 48604207 48604207 48604207 ACCTCAGGCGATCCACCCACCTCTGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCAGTACAC ACCTCAGGCGATCCACCCACCTCTGCCTCCCATAGTGCTGGGATTACAGGCATGAGCCAGTACAC A T STON1-GTF2A1L Ensembl:ENSG00000068781 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1194960694 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_26761 51217 RMVar_ID_51217 Human_SNP_ID_70904664 A-to-I Human chr2 + 48668576 48668576 48668576 CTGAAGAGTGAAGCGCAGTGACTTACGCCTGTAATCTCAGCACTTTGGGAGGCCGAGGCGGGCGG CTGAAGAGTGAAGCGCAGTGACTTACGCCTGTTATCTCAGCACTTTGGGAGGCCGAGGCGGGCGG A T STON1-GTF2A1L,GTF2A1L Ensembl:ENSG00000068781,Ensembl:ENSG00000242441 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs938026066 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_199732,RMVar_hsa_circ_199730,RMVar_hsa_circ_58754,RMVar_hsa_circ_354321,RMVar_hsa_circ_199731,RMVar_hsa_circ_369903,RMVar_hsa_circ_284923,RMVar_hsa_circ_324975 51218 RMVar_ID_51218 Human_SNP_ID_71072040 A-to-I Human chr2 - 49229761 49229761 49229761 CCACCGGCGTCAAAGTATTTAGCTGACTCGCTACACTCCACGGAAGCAATATGAAGTGATCTGCT CCACCGGCGTCAAAGTATTTAGCTGACTCGCTGCACTCCACGGAAGCAATATGAAGTGATCTGCT T C AC009975.2 Ensembl:ENSG00000282998 lincRNA intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs983287243 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_20437967 51219 RMVar_ID_51219 Human_SNP_ID_71358485 A-to-I Human chr2 - 50191135 50191135 50191135 AATCCCAGCTACCTAGGAGGCTGAGGTAGGAGAAAAGCTTGAACCTGGGAGGCGGAGGTTATAGT AATCCCAGCTACCTAGGAGGCTGAGGTAGGAGTAAAGCTTGAACCTGGGAGGCGGAGGTTATAGT T A NRXN1 Ensembl:ENSG00000179915 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1174094465 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6943,RMVar_hsa_circ_17909,RMVar_hsa_circ_47179,RMVar_hsa_circ_275756,RMVar_hsa_circ_309080,RMVar_hsa_circ_343603,RMVar_hsa_circ_36864,RMVar_hsa_circ_16483,RMVar_hsa_circ_284285,RMVar_hsa_circ_291180,RMVar_hsa_circ_294728,RMVar_hsa_circ_293440,RMVar_hsa_circ_321005,RMVar_hsa_circ_329867,RMVar_hsa_circ_307129,RMVar_hsa_circ_301810 51220 RMVar_ID_51220 Human_SNP_ID_71370750 A-to-I Human chr2 - 50232595 50232595 50232595 AGATCACAAGGTCAAGAGATGGAGACTATGCTAGCCAACAAGGTGAAACCCCATCTCTACTAAAA AGATCACAAGGTCAAGAGATGGAGACTATGCTTGCCAACAAGGTGAAACCCCATCTCTACTAAAA T A NRXN1 Ensembl:ENSG00000179915 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs953726065 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6943,RMVar_hsa_circ_17909,RMVar_hsa_circ_47179,RMVar_hsa_circ_275756,RMVar_hsa_circ_309080,RMVar_hsa_circ_343603,RMVar_hsa_circ_36864,RMVar_hsa_circ_16483,RMVar_hsa_circ_284285,RMVar_hsa_circ_291180,RMVar_hsa_circ_294728,RMVar_hsa_circ_293440,RMVar_hsa_circ_321005,RMVar_hsa_circ_329867,RMVar_hsa_circ_307129,RMVar_hsa_circ_301810 51221 RMVar_ID_51221 Human_SNP_ID_71371275 A-to-I Human chr2 - 50234447 50234447 50234447 TCTTGTTGCCCAGGCTGGAGTGCAATGATGCAATCTCAGTTCACTGCAACCTTTGCCTCCTGGGT TCTTGTTGCCCAGGCTGGAGTGCAATGATGCACTCTCAGTTCACTGCAACCTTTGCCTCCTGGGT T G NRXN1 Ensembl:ENSG00000179915 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs577738566 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6943,RMVar_hsa_circ_17909,RMVar_hsa_circ_47179,RMVar_hsa_circ_275756,RMVar_hsa_circ_309080,RMVar_hsa_circ_343603,RMVar_hsa_circ_36864,RMVar_hsa_circ_16483,RMVar_hsa_circ_284285,RMVar_hsa_circ_291180,RMVar_hsa_circ_294728,RMVar_hsa_circ_293440,RMVar_hsa_circ_321005,RMVar_hsa_circ_329867,RMVar_hsa_circ_307129,RMVar_hsa_circ_301810 51222 RMVar_ID_51222 Human_SNP_ID_71371278 A-to-I Human chr2 - 50234455 50234455 50234455 AGTTTCGCTCTTGTTGCCCAGGCTGGAGTGCAATGATGCAATCTCAGTTCACTGCAACCTTTGCC AGTTTCGCTCTTGTTGCCCAGGCTGGAGTGCAGTGATGCAATCTCAGTTCACTGCAACCTTTGCC T C NRXN1 Ensembl:ENSG00000179915 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs555174876 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6943,RMVar_hsa_circ_17909,RMVar_hsa_circ_47179,RMVar_hsa_circ_275756,RMVar_hsa_circ_309080,RMVar_hsa_circ_343603,RMVar_hsa_circ_36864,RMVar_hsa_circ_16483,RMVar_hsa_circ_284285,RMVar_hsa_circ_291180,RMVar_hsa_circ_294728,RMVar_hsa_circ_293440,RMVar_hsa_circ_321005,RMVar_hsa_circ_329867,RMVar_hsa_circ_307129,RMVar_hsa_circ_301810 51223 RMVar_ID_51223 Human_SNP_ID_71428706 A-to-I Human chr2 - 50428209 50428209 50428209 GGGGTCTTGCTGTGTTGCCCAGGTGGTCTTGAACTCCTGGACTCAAGTGATTCTCTCTCCTCAGC GGGGTCTTGCTGTGTTGCCCAGGTGGTCTTGACCTCCTGGACTCAAGTGATTCTCTCTCCTCAGC T G NRXN1 Ensembl:ENSG00000179915 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1337602945 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6943,RMVar_hsa_circ_17909,RMVar_hsa_circ_275756,RMVar_hsa_circ_309080,RMVar_hsa_circ_36864,RMVar_hsa_circ_16483,RMVar_hsa_circ_291180,RMVar_hsa_circ_294728,RMVar_hsa_circ_293440,RMVar_hsa_circ_321005,RMVar_hsa_circ_307129,RMVar_hsa_circ_301810,RMVar_hsa_circ_268420,RMVar_hsa_circ_292093,RMVar_hsa_circ_309127,RMVar_hsa_circ_323678,RMVar_hsa_circ_327433,RMVar_hsa_circ_318918,RMVar_hsa_circ_289804 51224 RMVar_ID_51224 Human_SNP_ID_71432023 A-to-I Human chr2 - 50439550 50439550 50439550 CACCCGCCTCGGCCTCCCAGGGTGCTGGGATTACAGGCGTGAGCCACCGCGCCCGGCCTTTTTTA CACCCGCCTCGGCCTCCCAGGGTGCTGGGATTGCAGGCGTGAGCCACCGCGCCCGGCCTTTTTTA T C NRXN1 Ensembl:ENSG00000179915 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1362918022 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23182828 RMVar_hsa_circ_6943,RMVar_hsa_circ_17909,RMVar_hsa_circ_275756,RMVar_hsa_circ_309080,RMVar_hsa_circ_36864,RMVar_hsa_circ_16483,RMVar_hsa_circ_291180,RMVar_hsa_circ_294728,RMVar_hsa_circ_293440,RMVar_hsa_circ_321005,RMVar_hsa_circ_307129,RMVar_hsa_circ_301810,RMVar_hsa_circ_268420,RMVar_hsa_circ_292093,RMVar_hsa_circ_309127,RMVar_hsa_circ_323678,RMVar_hsa_circ_327433,RMVar_hsa_circ_318918,RMVar_hsa_circ_289804 51225 RMVar_ID_51225 Human_SNP_ID_71454055 A-to-I Human chr2 - 50511199 50511199 50511199 AAAATTAGCTGGGCATGGTAGTGGGTGCCTGTAATCCCAGCTCCCTGGGAGGCTGAGGCAGGAGA AAAATTAGCTGGGCATGGTAGTGGGTGCCTGTTATCCCAGCTCCCTGGGAGGCTGAGGCAGGAGA T A NRXN1 Ensembl:ENSG00000179915 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1368330809 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_6943,RMVar_hsa_circ_36864,RMVar_hsa_circ_16483,RMVar_hsa_circ_294728,RMVar_hsa_circ_293440,RMVar_hsa_circ_321005,RMVar_hsa_circ_307129,RMVar_hsa_circ_268420,RMVar_hsa_circ_292093,RMVar_hsa_circ_323678,RMVar_hsa_circ_327433,RMVar_hsa_circ_318918,RMVar_hsa_circ_289804,RMVar_hsa_circ_268933,RMVar_hsa_circ_325373,RMVar_hsa_circ_329013,RMVar_hsa_circ_326906,RMVar_hsa_circ_307018,RMVar_hsa_circ_279431,RMVar_hsa_circ_199751,RMVar_hsa_circ_199752,RMVar_hsa_circ_199750,RMVar_hsa_circ_295343,RMVar_hsa_circ_329179,RMVar_hsa_circ_342233,RMVar_hsa_circ_308859,RMVar_hsa_circ_53258,RMVar_hsa_circ_199754,RMVar_hsa_circ_199755,RMVar_hsa_circ_312149,RMVar_hsa_circ_326022,RMVar_hsa_circ_333647,RMVar_hsa_circ_276891,RMVar_hsa_circ_287421,RMVar_hsa_circ_199760,RMVar_hsa_circ_199761,RMVar_hsa_circ_199762,RMVar_hsa_circ_199763,RMVar_hsa_circ_304609,RMVar_hsa_circ_320097,RMVar_hsa_circ_35984 51226 RMVar_ID_51226 Human_SNP_ID_71493851 A-to-I Human chr2 - 50646402 50646402 50646402 TTTTCCACCAGGCAAGAGTCACCCCAGTCACTAAACAAATTGACCAATTTCAGAGTATTTCCTGC TTTTCCACCAGGCAAGAGTCACCCCAGTCACTGAACAAATTGACCAATTTCAGAGTATTTCCTGC T C NRXN1 Ensembl:ENSG00000179915 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1192311165 Functional Loss SNV dbSNP153 33..33 33 - - - 51227 RMVar_ID_51227 Human_SNP_ID_71519511 A-to-I Human chr2 - 50736625 50736625 50736625 ATGAGAACCAAGCAAAAGGGGTTTCTCCCCTTATAAAACCATCAGATCTTGTGAGACTTATTCAC ATGAGAACCAAGCAAAAGGGGTTTCTCCCCTTGTAAAACCATCAGATCTTGTGAGACTTATTCAC T C NRXN1 Ensembl:ENSG00000179915 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1390637365 Functional Loss SNV dbSNP153 33..33 33 - - - 51228 RMVar_ID_51228 Human_SNP_ID_71522162 A-to-I Human chr2 - 50745910 50745910 50745910 GTTTTAAAATTTCCACCTGATATGGTTTAGCTATGTCCCCACCCAAATTTCATCTTGAATTGTAG GTTTTAAAATTTCCACCTGATATGGTTTAGCTGTGTCCCCACCCAAATTTCATCTTGAATTGTAG T C NRXN1 Ensembl:ENSG00000179915 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1029468627 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_199775 51229 RMVar_ID_51229 Human_SNP_ID_71541389 A-to-I Human chr2 - 50814276 50814276 50814276 AATTGAGAAGAAAGGCAGGTGTGGCAGCTCACATCTGTAATCCCAGCACTTTGGGAGGACAAGGC AATTGAGAAGAAAGGCAGGTGTGGCAGCTCACGTCTGTAATCCCAGCACTTTGGGAGGACAAGGC T C NRXN1 Ensembl:ENSG00000179915 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1286695517 Functional Loss SNV dbSNP153 33..33 33 - - - 51230 RMVar_ID_51230 Human_SNP_ID_71568981 A-to-I Human chr2 - 50911071 50911071 50911071 AGATAAATCTCTCAGTGGTCCCATCTGTTGCAATAAATCATGATGATAGTATTTGAAAGTGCCAC AGATAAATCTCTCAGTGGTCCCATCTGTTGCAGTAAATCATGATGATAGTATTTGAAAGTGCCAC T C NRXN1 Ensembl:ENSG00000179915 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs528839553 Functional Loss SNV dbSNP153 33..33 33 - - - 51231 RMVar_ID_51231 Human_SNP_ID_71568983 A-to-I Human chr2 - 50911081 50911081 50911081 CCCTTGCCAAAGATAAATCTCTCAGTGGTCCCATCTGTTGCAATAAATCATGATGATAGTATTTG CCCTTGCCAAAGATAAATCTCTCAGTGGTCCCGTCTGTTGCAATAAATCATGATGATAGTATTTG T C NRXN1 Ensembl:ENSG00000179915 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1421919110 Functional Loss SNV dbSNP153 33..33 33 - - - 51232 RMVar_ID_51232 Human_SNP_ID_71569325 A-to-I Human chr2 - 50912361 50912361 50912361 TTAAATCACATGCAATATGTAACCCTCTATGTATAGAGCTTCCCTAAATTCTGAAGTTGAGGAAC TTAAATCACATGCAATATGTAACCCTCTATGTGTAGAGCTTCCCTAAATTCTGAAGTTGAGGAAC T C NRXN1 Ensembl:ENSG00000179915 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1363753320 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_199783,RMVar_hsa_circ_199784,RMVar_hsa_circ_199785 51233 RMVar_ID_51233 Human_SNP_ID_71569328 A-to-I Human chr2 - 50912377 50912377 50912377 AATTTTTGGTACCATCTTAAATCACATGCAATATGTAACCCTCTATGTATAGAGCTTCCCTAAAT AATTTTTGGTACCATCTTAAATCACATGCAATCTGTAACCCTCTATGTATAGAGCTTCCCTAAAT T G NRXN1 Ensembl:ENSG00000179915 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs527360771 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_199783,RMVar_hsa_circ_199784,RMVar_hsa_circ_199785 51234 RMVar_ID_51234 Human_SNP_ID_71577548 A-to-I Human chr2 - 50941202 50941202 50941202 TTCATAAAGAGTTTAAATTGACTCAGAGTTCTACATGGCTGAGGAGGTCTCAAGAAACTTAAAAT TTCATAAAGAGTTTAAATTGACTCAGAGTTCTGCATGGCTGAGGAGGTCTCAAGAAACTTAAAAT T C NRXN1 Ensembl:ENSG00000179915 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1402263446 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_199787,RMVar_hsa_circ_199785 51235 RMVar_ID_51235 Human_SNP_ID_71577549 A-to-I Human chr2 - 50941202 50941202 50941202 TTCATAAAGAGTTTAAATTGACTCAGAGTTCTACATGGCTGAGGAGGTCTCAAGAAACTTAAAAT TTCATAAAGAGTTTAAATTGACTCAGAGTTCTCCATGGCTGAGGAGGTCTCAAGAAACTTAAAAT T G NRXN1 Ensembl:ENSG00000179915 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1402263446 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_199787,RMVar_hsa_circ_199785 51236 RMVar_ID_51236 Human_SNP_ID_71577556 A-to-I Human chr2 - 50941219 50941219 50941219 TACCCGAGACTCGGTAATTCATAAAGAGTTTAAATTGACTCAGAGTTCTACATGGCTGAGGAGGT TACCCGAGACTCGGTAATTCATAAAGAGTTTACATTGACTCAGAGTTCTACATGGCTGAGGAGGT T G NRXN1 Ensembl:ENSG00000179915 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1162958723 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_199787,RMVar_hsa_circ_199785 51237 RMVar_ID_51237 Human_SNP_ID_71577558 A-to-I Human chr2 - 50941228 50941226 50941228 ATAAAGAACTACCCGAGACTCGGTAATTCATAAAGAGTTTAAATTGACTCAGAGTTCTACATGGC ATAAAGAACTACCCGAGACTCGGTAATTCATA__GAGTTTAAATTGACTCAGAGTTCTACATGGC CTT C NRXN1 Ensembl:ENSG00000179915 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs779706420 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_199787,RMVar_hsa_circ_199785 51238 RMVar_ID_51238 Human_SNP_ID_71582188 A-to-I Human chr2 - 50956624 50956624 50956624 CCTGCCTCAGCCTCCTGAGTCGCTGGCACTATAGGCATGCACTACCACACCCAGCTAATTTTTGT CCTGCCTCAGCCTCCTGAGTCGCTGGCACTATGGGCATGCACTACCACACCCAGCTAATTTTTGT T C NRXN1 Ensembl:ENSG00000179915 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1317810062 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_199787,RMVar_hsa_circ_199785 51239 RMVar_ID_51239 Human_SNP_ID_71593982 A-to-I Human chr2 - 50997659 50997659 50997659 ATAATTTTTTTTTTTAATTACCTGGGTGTGGTAGTGTGCACCTGTAGTCATAGCTACTCAGGAAG ATAATTTTTTTTTTTAATTACCTGGGTGTGGTGGTGTGCACCTGTAGTCATAGCTACTCAGGAAG T C NRXN1 Ensembl:ENSG00000179915 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1026181056 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_199787,RMVar_hsa_circ_199785 51240 RMVar_ID_51240 Human_SNP_ID_71599612 A-to-I Human chr2 - 51017428 51017420 51017429 AGGAGGCTGAGGTGTGAAGATTGCTTGATCCCAGGAGTTCTAGGAGGCAGTGGGCTATTATTGTG AGGAGGCTGAGGTGTGAAGATTGCTTGATCC_________TAGGAGGCAGTGGGCTATTATTGTG AGAACTCCTG A NRXN1 Ensembl:ENSG00000179915 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs202197213 Functional Loss DEL dbSNP153 32..40 33 - - - 51241 RMVar_ID_51241 Human_SNP_ID_72310428 A-to-I Human chr2 - 53343892 53343892 53343892 ACTATAGTCTGGCTATTGTACTATCAAATATTAGAACTTATTTCTTCTATCTAGCTATATTTTTG ACTATAGTCTGGCTATTGTACTATCAAATATTGGAACTTATTTCTTCTATCTAGCTATATTTTTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs953404986 Functional Loss SNV dbSNP153 33..33 33 - - - 51242 RMVar_ID_51242 Human_SNP_ID_72401579 A-to-I Human chr2 - 53662672 53662672 53662672 AAGGAACTGATTCTGCTTACTATTTCTGTCACATTGGTAGAAAATGTATAGCCCCTATTTGCAAC AAGGAACTGATTCTGCTTACTATTTCTGTCACGTTGGTAGAAAATGTATAGCCCCTATTTGCAAC T C ASB3 Ensembl:ENSG00000115239 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs540722253 Functional Loss SNV dbSNP153 33..33 33 - - - 51243 RMVar_ID_51243 Human_SNP_ID_72410583 A-to-I Human chr2 - 53693897 53693897 53693897 CTCTCTGCTCGTGCCTCAAACGCTTGGATTCTACAGCAACATATTGGTAAGAAAGAATAACTTTT CTCTCTGCTCGTGCCTCAAACGCTTGGATTCTTCAGCAACATATTGGTAAGAAAGAATAACTTTT T A ASB3 Ensembl:ENSG00000115239 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1255524311 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9386463,Human_RBP_ID_18999417,Human_RBP_ID_23875596 Human_Splice_Rec_245163,Human_Splice_Rec_245195,Human_Splice_Rec_245213,Human_Splice_Rec_245231,Human_Splice_Rec_245247,Human_Splice_Rec_245263,Human_Splice_Rec_245265 RMVar_hsa_circ_199802,RMVar_hsa_circ_199806,RMVar_hsa_circ_275448,RMVar_hsa_circ_288283,RMVar_hsa_circ_297684,RMVar_hsa_circ_278937,RMVar_hsa_circ_271178,RMVar_hsa_circ_199804,RMVar_hsa_circ_199805,RMVar_hsa_circ_199803 51244 RMVar_ID_51244 Human_SNP_ID_72414146 A-to-I Human chr2 - 53706535 53706535 53706535 AGGCTGAAGCGGTAGAATGGCGTGAACCGGGGAGGCAGAGCTTGCAGTGAGCCAAGATCACGCCA AGGCTGAAGCGGTAGAATGGCGTGAACCGGGGGGGCAGAGCTTGCAGTGAGCCAAGATCACGCCA T C ASB3 Ensembl:ENSG00000115239 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs978229244 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_199808,RMVar_hsa_circ_199802,RMVar_hsa_circ_275448,RMVar_hsa_circ_297684,RMVar_hsa_circ_278937,RMVar_hsa_circ_271178,RMVar_hsa_circ_199804,RMVar_hsa_circ_199805,RMVar_hsa_circ_199803,RMVar_hsa_circ_273021,RMVar_hsa_circ_316442,RMVar_hsa_circ_87017,RMVar_hsa_circ_199809,RMVar_hsa_circ_199807 51245 RMVar_ID_51245 Human_SNP_ID_72414168 A-to-I Human chr2 - 53706586 53706586 53706586 AAAAAATTAGTCAGGCGTGGCGGCACGTGCCTATAGTCCCAACTACTCAGGAGGCTGAAGCGGTA AAAAAATTAGTCAGGCGTGGCGGCACGTGCCTGTAGTCCCAACTACTCAGGAGGCTGAAGCGGTA T C ASB3 Ensembl:ENSG00000115239 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1487706104 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_199808,RMVar_hsa_circ_199802,RMVar_hsa_circ_275448,RMVar_hsa_circ_297684,RMVar_hsa_circ_278937,RMVar_hsa_circ_271178,RMVar_hsa_circ_199804,RMVar_hsa_circ_199805,RMVar_hsa_circ_199803,RMVar_hsa_circ_273021,RMVar_hsa_circ_316442,RMVar_hsa_circ_87017,RMVar_hsa_circ_199809,RMVar_hsa_circ_199807 51246 RMVar_ID_51246 Human_SNP_ID_72414448 A-to-I Human chr2 - 53707548 53707548 53707548 CTGCCTCCTGGGTTCATGCCATTCTCCACCTCAGCCTCCCGAGTAGCTGGGACTACAGGTGCCCG CTGCCTCCTGGGTTCATGCCATTCTCCACCTCTGCCTCCCGAGTAGCTGGGACTACAGGTGCCCG T A ASB3 Ensembl:ENSG00000115239 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1214379884 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_199808,RMVar_hsa_circ_199802,RMVar_hsa_circ_275448,RMVar_hsa_circ_297684,RMVar_hsa_circ_278937,RMVar_hsa_circ_271178,RMVar_hsa_circ_199804,RMVar_hsa_circ_199805,RMVar_hsa_circ_199803,RMVar_hsa_circ_273021,RMVar_hsa_circ_316442,RMVar_hsa_circ_87017,RMVar_hsa_circ_199809,RMVar_hsa_circ_199807 51247 RMVar_ID_51247 Human_SNP_ID_72422292 A-to-I Human chr2 - 53733534 53733534 53733534 GGGAGGCTGACGCAGGAGAACCGCTTGAACCCAGGAGACAGAGGTTGCTGTGAGCCGAAATAGTG GGGAGGCTGACGCAGGAGAACCGCTTGAACCCGGGAGACAGAGGTTGCTGTGAGCCGAAATAGTG T C ASB3 Ensembl:ENSG00000115239 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1380461609 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13910966 RMVar_hsa_circ_199808,RMVar_hsa_circ_199802,RMVar_hsa_circ_275448,RMVar_hsa_circ_297684,RMVar_hsa_circ_199803,RMVar_hsa_circ_273021,RMVar_hsa_circ_316442,RMVar_hsa_circ_199809,RMVar_hsa_circ_199813,RMVar_hsa_circ_288784,RMVar_hsa_circ_296416,RMVar_hsa_circ_199812,RMVar_hsa_circ_199816,RMVar_hsa_circ_304530,RMVar_hsa_circ_281724,RMVar_hsa_circ_199817,RMVar_hsa_circ_199818,RMVar_hsa_circ_199815,RMVar_hsa_circ_338311 51248 RMVar_ID_51248 Human_SNP_ID_72435345 A-to-I Human chr2 - 53777981 53777981 53777981 CCACACCTGGCTAATTTTTTTGTATTTTTGGTAGAGACGGGGTTTCACCATATTGGTCAGGCAGG CCACACCTGGCTAATTTTTTTGTATTTTTGGTGGAGACGGGGTTTCACCATATTGGTCAGGCAGG T C ASB3 Ensembl:ENSG00000115239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1359544056 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_199815 51249 RMVar_ID_51249 Human_SNP_ID_72435374 A-to-I Human chr2 - 53778086 53778086 53778086 GGAGTGCAGTGGCGCCATCTTGGCTCACTGCAACCTCTGCCTCCTGGGTTCAAGCAATTCTCCTG GGAGTGCAGTGGCGCCATCTTGGCTCACTGCATCCTCTGCCTCCTGGGTTCAAGCAATTCTCCTG T A ASB3 Ensembl:ENSG00000115239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs996387549 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_199815 51250 RMVar_ID_51250 Human_SNP_ID_72435375 A-to-I Human chr2 - 53778086 53778086 53778086 GGAGTGCAGTGGCGCCATCTTGGCTCACTGCAACCTCTGCCTCCTGGGTTCAAGCAATTCTCCTG GGAGTGCAGTGGCGCCATCTTGGCTCACTGCAGCCTCTGCCTCCTGGGTTCAAGCAATTCTCCTG T C ASB3 Ensembl:ENSG00000115239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs996387549 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_199815 51251 RMVar_ID_51251 Human_SNP_ID_72435997 A-to-I Human chr2 - 53780613 53780613 53780613 CCACTATGCCCAGCTAATTTTTACATTTTTGTAGAGACATGGTCTCACTATATTGCCCAGGCTGG CCACTATGCCCAGCTAATTTTTACATTTTTGTGGAGACATGGTCTCACTATATTGCCCAGGCTGG T C ASB3 Ensembl:ENSG00000115239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs922664029 Functional Loss SNV dbSNP153 33..33 33 - - - 51252 RMVar_ID_51252 Human_SNP_ID_72436009 A-to-I Human chr2 - 53780662 53780662 53780662 GAGATCCTTCTGCTTTATCCTCCAGAGTGGCTAGGACTGCAGACATGTGCCACTATGCCCAGCTA GAGATCCTTCTGCTTTATCCTCCAGAGTGGCTGGGACTGCAGACATGTGCCACTATGCCCAGCTA T C ASB3 Ensembl:ENSG00000115239 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1317673032 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13911643 51253 RMVar_ID_51253 Human_SNP_ID_72436189 A-to-I Human chr2 - 53781381 53781381 53781381 TGGAGACAGAGTCTCACTTTGTTGCCTAGACTAGAGTGCAATGGCATGGTTTTGGCTCATTGTAG TGGAGACAGAGTCTCACTTTGTTGCCTAGACTGGAGTGCAATGGCATGGTTTTGGCTCATTGTAG T C ASB3 Ensembl:ENSG00000115239 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1030220475 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569600 51254 RMVar_ID_51254 Human_SNP_ID_72455191 A-to-I Human chr2 - 53849195 53849195 53849195 AGAGACATAACTTCTTTCTTCGTAAGTTATATATGTCTACTTCTACCTGTGTTATCATAATAAAG AGAGACATAACTTCTTTCTTCGTAAGTTATATGTGTCTACTTCTACCTGTGTTATCATAATAAAG T C ASB3,MIR3682 Ensembl:ENSG00000115239,Ensembl:ENSG00000265452 Protein coding,miRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1047873 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1919376 51255 RMVar_ID_51255 Human_SNP_ID_72455192 A-to-I Human chr2 - 53849197 53849197 53849197 ATAGAGACATAACTTCTTTCTTCGTAAGTTATATATGTCTACTTCTACCTGTGTTATCATAATAA ATAGAGACATAACTTCTTTCTTCGTAAGTTATGTATGTCTACTTCTACCTGTGTTATCATAATAA T C ASB3,MIR3682 Ensembl:ENSG00000115239,Ensembl:ENSG00000265452 Protein coding,miRNA intron,exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs966159718 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1919376 51256 RMVar_ID_51256 Human_SNP_ID_72455532 A-to-I Human chr2 - 53850523 53850523 53850523 GGTGCCCGCCACCACTCCTGGCTAATTTTTGTATTTTTGGTAGAGACAGGGTTTCACCATGATAG GGTGCCCGCCACCACTCCTGGCTAATTTTTGTGTTTTTGGTAGAGACAGGGTTTCACCATGATAG T C ASB3 Ensembl:ENSG00000115239 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs536303754 Functional Loss SNV dbSNP153 33..33 33 - - - 51257 RMVar_ID_51257 Human_SNP_ID_72455543 A-to-I Human chr2 - 53850580 53850580 53850580 CGCTTCCCGGGTTCAAGCGATTGTCTTGCCTCAGCCTCCAGAGTAGCTGGGATTACAGGTGCCCG CGCTTCCCGGGTTCAAGCGATTGTCTTGCCTCGGCCTCCAGAGTAGCTGGGATTACAGGTGCCCG T C ASB3 Ensembl:ENSG00000115239 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs953362501 Functional Loss SNV dbSNP153 33..33 33 - - - 51258 RMVar_ID_51258 Human_SNP_ID_72455560 A-to-I Human chr2 - 53850649 53850649 53850649 TAGAAACAGAGTCTTACTCTGTCACCCAGGCTAAAGTGCAGTGGCATGATCTCAGATCGCTGCAA TAGAAACAGAGTCTTACTCTGTCACCCAGGCTGAAGTGCAGTGGCATGATCTCAGATCGCTGCAA T C ASB3 Ensembl:ENSG00000115239 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053886045 Functional Loss SNV dbSNP153 33..33 33 - - - 51259 RMVar_ID_51259 Human_SNP_ID_72455718 A-to-I Human chr2 - 53851363 53851363 53851363 CCTCGGCCTCCCGAAGTGCTGGGATTACAGGCATGAGCCACCCCAACTGGCCCAAAAGTGAATTG CCTCGGCCTCCCGAAGTGCTGGGATTACAGGCGTGAGCCACCCCAACTGGCCCAAAAGTGAATTG T C ASB3 Ensembl:ENSG00000115239 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025881045 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8520973 51260 RMVar_ID_51260 Human_SNP_ID_72455735 A-to-I Human chr2 - 53851409 53851409 53851409 AGGTCTTGAACTTGTCTTGAACTCCTGACCTCAGGTGATCTGCCTGCCTCGGCCTCCCGAAGTGC AGGTCTTGAACTTGTCTTGAACTCCTGACCTCTGGTGATCTGCCTGCCTCGGCCTCCCGAAGTGC T A ASB3 Ensembl:ENSG00000115239 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1216894856 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8520974,Human_RBP_ID_18762205 51261 RMVar_ID_51261 Human_SNP_ID_72455843 A-to-I Human chr2 - 53851762 53851762 53851762 AGAGAATCGCTTGAACCTGGGAGACAGGTTGCAGTGAGCTGAGATCGTGCCATTGCACTCCAGCC AGAGAATCGCTTGAACCTGGGAGACAGGTTGCGGTGAGCTGAGATCGTGCCATTGCACTCCAGCC T C ASB3 Ensembl:ENSG00000115239 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1287248807 Functional Loss SNV dbSNP153 33..33 33 - - - 51262 RMVar_ID_51262 Human_SNP_ID_72455844 A-to-I Human chr2 - 53851762 53851762 53851762 AGAGAATCGCTTGAACCTGGGAGACAGGTTGCAGTGAGCTGAGATCGTGCCATTGCACTCCAGCC AGAGAATCGCTTGAACCTGGGAGACAGGTTGCCGTGAGCTGAGATCGTGCCATTGCACTCCAGCC T G ASB3 Ensembl:ENSG00000115239 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1287248807 Functional Loss SNV dbSNP153 33..33 33 - - - 51263 RMVar_ID_51263 Human_SNP_ID_72461454 A-to-I Human chr2 - 53870662 53870662 53870662 TATGAAAATAAACTTTGGTGGCTGGGTGCGGTAGCTCATGCCTGTAATCGCAGCACTTTAGGAGG TATGAAAATAAACTTTGGTGGCTGGGTGCGGTGGCTCATGCCTGTAATCGCAGCACTTTAGGAGG T C PSME4 Ensembl:ENSG00000068878 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1197757482 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13912324,Human_RBP_ID_25548841 RMVar_hsa_circ_11144,RMVar_hsa_circ_92924,RMVar_hsa_circ_123564,RMVar_hsa_circ_199835,RMVar_hsa_circ_199836,RMVar_hsa_circ_364483,RMVar_hsa_circ_375164,RMVar_hsa_circ_363316,RMVar_hsa_circ_337210,RMVar_hsa_circ_337897,RMVar_hsa_circ_325293,RMVar_hsa_circ_23326,RMVar_hsa_circ_87185,RMVar_hsa_circ_97568,RMVar_hsa_circ_84644,RMVar_hsa_circ_17812,RMVar_hsa_circ_22837,RMVar_hsa_circ_15301,RMVar_hsa_circ_4611,RMVar_hsa_circ_35546,RMVar_hsa_circ_199840,RMVar_hsa_circ_199842,RMVar_hsa_circ_5749,RMVar_hsa_circ_199841,RMVar_hsa_circ_199838,RMVar_hsa_circ_199839,RMVar_hsa_circ_199837,RMVar_hsa_circ_319951,RMVar_hsa_circ_199844,RMVar_hsa_circ_314043,RMVar_hsa_circ_48645,RMVar_hsa_circ_199846 51264 RMVar_ID_51264 Human_SNP_ID_72461634 A-to-I Human chr2 - 53871323 53871323 53871323 TGGCATCAACCCAGGATGTGGAGCTTGCAGTGAGCCAAGATCGTGCCACTGCACTCCATCCTGGT TGGCATCAACCCAGGATGTGGAGCTTGCAGTGTGCCAAGATCGTGCCACTGCACTCCATCCTGGT T A PSME4 Ensembl:ENSG00000068878 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1373554002 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13912337 RMVar_hsa_circ_11144,RMVar_hsa_circ_92924,RMVar_hsa_circ_123564,RMVar_hsa_circ_199835,RMVar_hsa_circ_199836,RMVar_hsa_circ_364483,RMVar_hsa_circ_375164,RMVar_hsa_circ_363316,RMVar_hsa_circ_337210,RMVar_hsa_circ_337897,RMVar_hsa_circ_325293,RMVar_hsa_circ_23326,RMVar_hsa_circ_87185,RMVar_hsa_circ_97568,RMVar_hsa_circ_84644,RMVar_hsa_circ_17812,RMVar_hsa_circ_22837,RMVar_hsa_circ_15301,RMVar_hsa_circ_4611,RMVar_hsa_circ_35546,RMVar_hsa_circ_199840,RMVar_hsa_circ_199842,RMVar_hsa_circ_5749,RMVar_hsa_circ_199841,RMVar_hsa_circ_199838,RMVar_hsa_circ_199839,RMVar_hsa_circ_199837,RMVar_hsa_circ_319951,RMVar_hsa_circ_199844,RMVar_hsa_circ_314043,RMVar_hsa_circ_48645,RMVar_hsa_circ_199846 51265 RMVar_ID_51265 Human_SNP_ID_72461643 A-to-I Human chr2 - 53871361 53871361 53871361 CTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAAGAGAATGGCATCAACCCAGGATGTGGAGCTTG CTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATGGCATCAACCCAGGATGTGGAGCTTG T C PSME4 Ensembl:ENSG00000068878 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1326495032 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11144,RMVar_hsa_circ_92924,RMVar_hsa_circ_123564,RMVar_hsa_circ_199835,RMVar_hsa_circ_199836,RMVar_hsa_circ_364483,RMVar_hsa_circ_375164,RMVar_hsa_circ_363316,RMVar_hsa_circ_337210,RMVar_hsa_circ_337897,RMVar_hsa_circ_325293,RMVar_hsa_circ_23326,RMVar_hsa_circ_87185,RMVar_hsa_circ_97568,RMVar_hsa_circ_84644,RMVar_hsa_circ_17812,RMVar_hsa_circ_22837,RMVar_hsa_circ_15301,RMVar_hsa_circ_4611,RMVar_hsa_circ_35546,RMVar_hsa_circ_199840,RMVar_hsa_circ_199842,RMVar_hsa_circ_5749,RMVar_hsa_circ_199841,RMVar_hsa_circ_199838,RMVar_hsa_circ_199839,RMVar_hsa_circ_199837,RMVar_hsa_circ_319951,RMVar_hsa_circ_199844,RMVar_hsa_circ_314043,RMVar_hsa_circ_48645,RMVar_hsa_circ_199846 51266 RMVar_ID_51266 Human_SNP_ID_72461660 A-to-I Human chr2 - 53871435 53871435 53871435 CCTGGCTAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAAAATTAGCCAGGCGTGGCAGC CCTGGCTAACATGGTGAAACCCCATCTCTACTGAAAATACAAAAAAATTAGCCAGGCGTGGCAGC T C PSME4 Ensembl:ENSG00000068878 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1056381480 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11144,RMVar_hsa_circ_92924,RMVar_hsa_circ_123564,RMVar_hsa_circ_199835,RMVar_hsa_circ_199836,RMVar_hsa_circ_364483,RMVar_hsa_circ_375164,RMVar_hsa_circ_363316,RMVar_hsa_circ_337210,RMVar_hsa_circ_337897,RMVar_hsa_circ_325293,RMVar_hsa_circ_23326,RMVar_hsa_circ_87185,RMVar_hsa_circ_97568,RMVar_hsa_circ_84644,RMVar_hsa_circ_17812,RMVar_hsa_circ_22837,RMVar_hsa_circ_15301,RMVar_hsa_circ_4611,RMVar_hsa_circ_35546,RMVar_hsa_circ_199840,RMVar_hsa_circ_199842,RMVar_hsa_circ_5749,RMVar_hsa_circ_199841,RMVar_hsa_circ_199838,RMVar_hsa_circ_199839,RMVar_hsa_circ_199837,RMVar_hsa_circ_319951,RMVar_hsa_circ_199844,RMVar_hsa_circ_314043,RMVar_hsa_circ_48645,RMVar_hsa_circ_199846 51267 RMVar_ID_51267 Human_SNP_ID_72462483 A-to-I Human chr2 - 53874197 53874197 53874197 TCAACTCTTTGAGAGACGAAGTCAGTGAGATCACTTGATGCCAGGAGTTTGAGACCAGCCTGGAC TCAACTCTTTGAGAGACGAAGTCAGTGAGATCTCTTGATGCCAGGAGTTTGAGACCAGCCTGGAC T A PSME4 Ensembl:ENSG00000068878 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs974008148 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25548867 RMVar_hsa_circ_11144,RMVar_hsa_circ_92924,RMVar_hsa_circ_123564,RMVar_hsa_circ_199835,RMVar_hsa_circ_199836,RMVar_hsa_circ_364483,RMVar_hsa_circ_375164,RMVar_hsa_circ_363316,RMVar_hsa_circ_337210,RMVar_hsa_circ_337897,RMVar_hsa_circ_325293,RMVar_hsa_circ_23326,RMVar_hsa_circ_87185,RMVar_hsa_circ_97568,RMVar_hsa_circ_84644,RMVar_hsa_circ_17812,RMVar_hsa_circ_22837,RMVar_hsa_circ_15301,RMVar_hsa_circ_4611,RMVar_hsa_circ_35546,RMVar_hsa_circ_199840,RMVar_hsa_circ_199842,RMVar_hsa_circ_5749,RMVar_hsa_circ_199841,RMVar_hsa_circ_199838,RMVar_hsa_circ_199839,RMVar_hsa_circ_199837,RMVar_hsa_circ_319951,RMVar_hsa_circ_199844,RMVar_hsa_circ_314043,RMVar_hsa_circ_48645,RMVar_hsa_circ_199846 51268 RMVar_ID_51268 Human_SNP_ID_72467175 A-to-I Human chr2 - 53891631 53891631 53891631 GGTCTCGAACTCCTGGCTCTTGAACTCCACCTACCTTGGCCTCCCAAAGTGCTGGGATTACAGGT GGTCTCGAACTCCTGGCTCTTGAACTCCACCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGT T C PSME4 Ensembl:ENSG00000068878 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs960707598 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13912624,Human_RBP_ID_25589672 RMVar_hsa_circ_11144,RMVar_hsa_circ_92924,RMVar_hsa_circ_199836,RMVar_hsa_circ_364483,RMVar_hsa_circ_375164,RMVar_hsa_circ_337897,RMVar_hsa_circ_87185,RMVar_hsa_circ_97568,RMVar_hsa_circ_17812,RMVar_hsa_circ_22837,RMVar_hsa_circ_199840,RMVar_hsa_circ_199838,RMVar_hsa_circ_199839,RMVar_hsa_circ_199837,RMVar_hsa_circ_319951,RMVar_hsa_circ_199844,RMVar_hsa_circ_314043,RMVar_hsa_circ_199846,RMVar_hsa_circ_351102,RMVar_hsa_circ_351713,RMVar_hsa_circ_362407,RMVar_hsa_circ_331882,RMVar_hsa_circ_11065,RMVar_hsa_circ_48498,RMVar_hsa_circ_103019,RMVar_hsa_circ_353805,RMVar_hsa_circ_100149,RMVar_hsa_circ_69385,RMVar_hsa_circ_107822,RMVar_hsa_circ_199849,RMVar_hsa_circ_199850,RMVar_hsa_circ_275504,RMVar_hsa_circ_26588,RMVar_hsa_circ_24916,RMVar_hsa_circ_32537,RMVar_hsa_circ_199851,RMVar_hsa_circ_199852,RMVar_hsa_circ_47021,RMVar_hsa_circ_50320,RMVar_hsa_circ_265393,RMVar_hsa_circ_70982,RMVar_hsa_circ_325156,RMVar_hsa_circ_349441,RMVar_hsa_circ_9241,RMVar_hsa_circ_347675,RMVar_hsa_circ_306389,RMVar_hsa_circ_36769,RMVar_hsa_circ_199853 51269 RMVar_ID_51269 Human_SNP_ID_72474726 A-to-I Human chr2 - 53918480 53918460 53918480 AAAATGAGCTGGACGTGGTGGCGCATACCTGTAGTCCCAGCTGAGGTGGGAGGATTGCTTGAGCC AAAATGAGCTGGACGTGGTGGCGCATACCTGT____________________GATTGCTTGAGCC CCTCCCACCTCAGCTGGGACT C PSME4 Ensembl:ENSG00000068878 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1302874906 Functional Loss DEL dbSNP153 33..52 33 - - - Human_RBP_ID_6929825,Human_RBP_ID_13913065 RMVar_hsa_circ_8300,RMVar_hsa_circ_92924,RMVar_hsa_circ_199836,RMVar_hsa_circ_375164,RMVar_hsa_circ_337897,RMVar_hsa_circ_199837,RMVar_hsa_circ_351713,RMVar_hsa_circ_11065,RMVar_hsa_circ_69385,RMVar_hsa_circ_265393,RMVar_hsa_circ_70982,RMVar_hsa_circ_347675,RMVar_hsa_circ_33432,RMVar_hsa_circ_10401,RMVar_hsa_circ_376222,RMVar_hsa_circ_199858,RMVar_hsa_circ_55513,RMVar_hsa_circ_92071,RMVar_hsa_circ_199861,RMVar_hsa_circ_45217,RMVar_hsa_circ_27110,RMVar_hsa_circ_53360,RMVar_hsa_circ_56904,RMVar_hsa_circ_56666,RMVar_hsa_circ_51208,RMVar_hsa_circ_199864,RMVar_hsa_circ_199865,RMVar_hsa_circ_65481,RMVar_hsa_circ_70396,RMVar_hsa_circ_378961,RMVar_hsa_circ_55484 51270 RMVar_ID_51270 Human_SNP_ID_72482785 A-to-I Human chr2 - 53943795 53943795 53943795 TGTTGTTGCCCAGGCTGGAGTGCAGTGGCACAATCTGGACTCACCGCAACCTCCGCCTCCCGAGT TGTTGTTGCCCAGGCTGGAGTGCAGTGGCACAGTCTGGACTCACCGCAACCTCCGCCTCCCGAGT T C PSME4 Ensembl:ENSG00000068878 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs907095076 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13913610 RMVar_hsa_circ_92924,RMVar_hsa_circ_199836,RMVar_hsa_circ_337897,RMVar_hsa_circ_265393,RMVar_hsa_circ_70982,RMVar_hsa_circ_56904,RMVar_hsa_circ_284972,RMVar_hsa_circ_40089,RMVar_hsa_circ_199880,RMVar_hsa_circ_106347,RMVar_hsa_circ_292864,RMVar_hsa_circ_199881,RMVar_hsa_circ_337628,RMVar_hsa_circ_199884,RMVar_hsa_circ_199886,RMVar_hsa_circ_356341,RMVar_hsa_circ_330908,RMVar_hsa_circ_365856,RMVar_hsa_circ_319017 51271 RMVar_ID_51271 Human_SNP_ID_72485438 A-to-I Human chr2 - 53952455 53952455 53952455 CAGCTGCAACCTCCGCCTCCCAGGTTCAAACAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGA CAGCTGCAACCTCCGCCTCCCAGGTTCAAACAGTTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGA T C PSME4 Ensembl:ENSG00000068878 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs558958916 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92924,RMVar_hsa_circ_199836 51272 RMVar_ID_51272 Human_SNP_ID_72489307 A-to-I Human chr2 - 53965291 53965291 53965291 TGAGCCGAGATGGCGCCACTGCACTCCAGGCTAGGCGACAGAGGGAGACTCTTGTCTTACAAAAA TGAGCCGAGATGGCGCCACTGCACTCCAGGCTGGGCGACAGAGGGAGACTCTTGTCTTACAAAAA T C PSME4 Ensembl:ENSG00000068878 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs998862142 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92924,RMVar_hsa_circ_199836 51273 RMVar_ID_51273 Human_SNP_ID_72492681 A-to-I Human chr2 + 53974188 53974188 53974188 CGCCCGCCTTGGACTCCCAAAGTGTTGGGATTACAGGCTTGAGCCACTGAGCCCGGCCATATTTA CGCCCGCCTTGGACTCCCAAAGTGTTGGGATTGCAGGCTTGAGCCACTGAGCCCGGCCATATTTA A G ACYP2 Ensembl:ENSG00000170634 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1019385393 Functional Loss SNV dbSNP153 33..33 33 - - - 51274 RMVar_ID_51274 Human_SNP_ID_72494448 A-to-I Human chr2 + 53980188 53980188 53980188 ACCAAGAGGCAACATAGCAAGACTCCATCTCTACAAAAAATTTAAAAATTAGCCAGGCGTTATGG ACCAAGAGGCAACATAGCAAGACTCCATCTCTTCAAAAAATTTAAAAATTAGCCAGGCGTTATGG A T ACYP2 Ensembl:ENSG00000170634 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs766938259 Functional Loss SNV dbSNP153 33..33 33 - - - 51275 RMVar_ID_51275 Human_SNP_ID_72500662 A-to-I Human chr2 + 54001262 54001262 54001262 CTACCATAGTAGTCCTAGCCACTTGAGAGGCTAAGGTGGGAGGAATACTTGGGTCTGGGTGTTTG CTACCATAGTAGTCCTAGCCACTTGAGAGGCTGAGGTGGGAGGAATACTTGGGTCTGGGTGTTTG A G ACYP2 Ensembl:ENSG00000170634 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1287472771 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9108420,Human_RBP_ID_17569611 51276 RMVar_ID_51276 Human_SNP_ID_72515398 A-to-I Human chr2 + 54051001 54051001 54051001 CGCTGTTCTACCTAGGCTGTTCTAGAACTCCTAATGTCAAGCTATCCTCCTGCCTCGGCCTCCCA CGCTGTTCTACCTAGGCTGTTCTAGAACTCCTCATGTCAAGCTATCCTCCTGCCTCGGCCTCCCA A C ACYP2 Ensembl:ENSG00000170634 Protein coding exon GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-Seq:(High) rs1428149110 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_245624,Human_Splice_Rec_245625,Human_Splice_Rec_245632,Human_Splice_Rec_245633,Human_Splice_Rec_245640,Human_Splice_Rec_245641 RMVar_hsa_circ_199888,RMVar_hsa_circ_199889,RMVar_hsa_circ_289828,RMVar_hsa_circ_337102,RMVar_hsa_circ_199890 51277 RMVar_ID_51277 Human_SNP_ID_72523488 A-to-I Human chr2 + 54082282 54082282 54082282 TTTCTTTTTTTTTTGAGATGAAGTCTCACTCTATCGCCCAGGCTGGAGTGCAGTGGTGTGGTCTC TTTCTTTTTTTTTTGAGATGAAGTCTCACTCTGTCGCCCAGGCTGGAGTGCAGTGGTGTGGTCTC A G ACYP2 Ensembl:ENSG00000170634 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277168483 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_337102 51278 RMVar_ID_51278 Human_SNP_ID_72542407 A-to-I Human chr2 + 54149041 54149041 54149041 TGAGGGGTGAGGTGGGTGGATTGCTTGAGCTCAAGAATTCGTGACCAGCCTGGGCAACATGATGA TGAGGGGTGAGGTGGGTGGATTGCTTGAGCTCGAGAATTCGTGACCAGCCTGGGCAACATGATGA A G ACYP2 Ensembl:ENSG00000170634 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1465672372 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56973 51279 RMVar_ID_51279 Human_SNP_ID_72549715 A-to-I Human chr2 + 54176060 54176060 54176060 CCCTTATCAGGCACTGAATCTATTGGTGCCTCAATCTTGGAATTCCTGGCACCCAGAATTGTGAG CCCTTATCAGGCACTGAATCTATTGGTGCCTCCATCTTGGAATTCCTGGCACCCAGAATTGTGAG A C ACYP2 Ensembl:ENSG00000170634 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs182272945 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56973 51280 RMVar_ID_51280 Human_SNP_ID_72549716 A-to-I Human chr2 + 54176060 54176060 54176060 CCCTTATCAGGCACTGAATCTATTGGTGCCTCAATCTTGGAATTCCTGGCACCCAGAATTGTGAG CCCTTATCAGGCACTGAATCTATTGGTGCCTCGATCTTGGAATTCCTGGCACCCAGAATTGTGAG A G ACYP2 Ensembl:ENSG00000170634 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs182272945 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56973 51281 RMVar_ID_51281 Human_SNP_ID_72560498 A-to-I Human chr2 + 54213845 54213845 54213845 GCTGGAGTGCAGTGGCATGAACGCTGCTCACTATAGCCTCAACCTCCCGGGCCCAAGCGATCCTC GCTGGAGTGCAGTGGCATGAACGCTGCTCACTGTAGCCTCAACCTCCCGGGCCCAAGCGATCCTC A G ACYP2 Ensembl:ENSG00000170634 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs942744737 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56973 51282 RMVar_ID_51282 Human_SNP_ID_72628619 A-to-I Human chr2 + 54467494 54467494 54467494 TCGGCTCACTGCAACCTCCGCCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGC TCGGCTCACTGCAACCTCCGCCTCCCAGGTTCGAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGC A G SPTBN1 Ensembl:ENSG00000115306 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1043391036 Functional Loss SNV dbSNP153 33..33 33 - - - 51283 RMVar_ID_51283 Human_SNP_ID_72628622 A-to-I Human chr2 + 54467499 54467499 54467499 TCACTGCAACCTCCGCCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGCG TCACTGCAACCTCCGCCTCCCAGGTTCAAGCGGTTCTCCTGCCTCAGCCTCCCGAGTAGCTGGCG A G SPTBN1 Ensembl:ENSG00000115306 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs902221576 Functional Loss SNV dbSNP153 33..33 33 - - - 51284 RMVar_ID_51284 Human_SNP_ID_72628623 A-to-I Human chr2 + 54467499 54467499 54467499 TCACTGCAACCTCCGCCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGCG TCACTGCAACCTCCGCCTCCCAGGTTCAAGCGTTTCTCCTGCCTCAGCCTCCCGAGTAGCTGGCG A T SPTBN1 Ensembl:ENSG00000115306 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs902221576 Functional Loss SNV dbSNP153 33..33 33 - - - 51285 RMVar_ID_51285 Human_SNP_ID_72628850 A-to-I Human chr2 + 54468148 54468148 54468148 GGCCAACATAGTGAAACTTTGTCTCTACTAAAAATGCAAAAATTGGCTGGGTGTGGTGGTGGGCT GGCCAACATAGTGAAACTTTGTCTCTACTAAATATGCAAAAATTGGCTGGGTGTGGTGGTGGGCT A T SPTBN1 Ensembl:ENSG00000115306 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs995851682 Functional Loss SNV dbSNP153 33..33 33 - - - 51286 RMVar_ID_51286 Human_SNP_ID_72631310 A-to-I Human chr2 + 54476378 54476378 54476378 TCTAACTAAACATAGATAACAGAGTAGGTAATATGGTCGAATCCAGCATTTCCCATCAGCTTCTT TCTAACTAAACATAGATAACAGAGTAGGTAATGTGGTCGAATCCAGCATTTCCCATCAGCTTCTT A G SPTBN1 Ensembl:ENSG00000115306 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1157034758 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17570726 51287 RMVar_ID_51287 Human_SNP_ID_72633595 A-to-I Human chr2 + 54484056 54484056 54484056 GTCTCTGCAAAAAATACAAAAATTGGCTGGGCATGGTGGTATGTGCCTGTGCCTTGGGAGGCTGA GTCTCTGCAAAAAATACAAAAATTGGCTGGGCGTGGTGGTATGTGCCTGTGCCTTGGGAGGCTGA A G SPTBN1 Ensembl:ENSG00000115306 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1044783774 Functional Loss SNV dbSNP153 33..33 33 - - - 51288 RMVar_ID_51288 Human_SNP_ID_72635692 A-to-I Human chr2 + 54489549 54489549 54489549 ATGGTGAAACCCCGTCTTACTAAAAATACAAAAATTAGCCAGGCGTGGTGGTGTGCATCTGTAAT ATGGTGAAACCCCGTCTTACTAAAAATACAAAGATTAGCCAGGCGTGGTGGTGTGCATCTGTAAT A G SPTBN1 Ensembl:ENSG00000115306 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1050297975 Functional Loss SNV dbSNP153 33..33 33 - - - 51289 RMVar_ID_51289 Human_SNP_ID_72648926 A-to-I Human chr2 + 54535746 54535746 54535746 TCTGTTGTAGGCATCAGAAACTACTGTAGGCCAGATGCAGTGGCTCACACCTGTAATCCCAGCCA TCTGTTGTAGGCATCAGAAACTACTGTAGGCCTGATGCAGTGGCTCACACCTGTAATCCCAGCCA A T SPTBN1 Ensembl:ENSG00000115306 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1452349607 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14578,RMVar_hsa_circ_59575,RMVar_hsa_circ_357360,RMVar_hsa_circ_123840,RMVar_hsa_circ_19749,RMVar_hsa_circ_199893 51290 RMVar_ID_51290 Human_SNP_ID_72786389 A-to-I Human chr2 - 54972435 54972435 54972435 ACCATCTGTTTTCAACATGAAATGCCACACACATAGAACTCCAACATCAATTTCATTGCACAGAC ACCATCTGTTTTCAACATGAAATGCCACACACGTAGAACTCCAACATCAATTTCATTGCACAGAC T C RTN4 Ensembl:ENSG00000115310 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs187115076 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_552357,Human_RBP_ID_17277637,Human_RBP_ID_17392642,Human_RBP_ID_17509656,Human_RBP_ID_22393823,Human_RBP_ID_22815768,Human_RBP_ID_24489652,Human_RBP_ID_27480662 RMVar_hsa_circ_121667,RMVar_hsa_circ_199950 51291 RMVar_ID_51291 Human_SNP_ID_72788313 A-to-I Human chr2 - 54978238 54978238 54978238 TTTAGAAGAGATGGGGTTTTGCCAAGTTGGCCAGACTGGTCTCGAACTCCTGACCTCAGGTGATC TTTAGAAGAGATGGGGTTTTGCCAAGTTGGCCGGACTGGTCTCGAACTCCTGACCTCAGGTGATC T C RTN4 Ensembl:ENSG00000115310 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1306307570 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_330678,RMVar_hsa_circ_265484,RMVar_hsa_circ_199953,RMVar_hsa_circ_273185 51292 RMVar_ID_51292 Human_SNP_ID_72788357 A-to-I Human chr2 - 54978354 54978354 54978354 CGATCTTAGGCTCACTGCAACCTTTGCCTTCCAGGTTCAAGTGATTCTCCTGCTTCAGCCTCCCA CGATCTTAGGCTCACTGCAACCTTTGCCTTCCGGGTTCAAGTGATTCTCCTGCTTCAGCCTCCCA T C RTN4 Ensembl:ENSG00000115310 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs779631688 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6930819 RMVar_hsa_circ_330678,RMVar_hsa_circ_265484,RMVar_hsa_circ_199953,RMVar_hsa_circ_273185 51293 RMVar_ID_51293 Human_SNP_ID_72788627 A-to-I Human chr2 - 54979119 54979119 54979119 AGCCCAGGAGGTGGAGGATGCAGTGAGCCATAATCATACCACTGCATTCCAGCCACGGCAACAGA AGCCCAGGAGGTGGAGGATGCAGTGAGCCATACTCATACCACTGCATTCCAGCCACGGCAACAGA T G RTN4 Ensembl:ENSG00000115310 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1003619801 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_330678,RMVar_hsa_circ_265484,RMVar_hsa_circ_199953,RMVar_hsa_circ_273185 51294 RMVar_ID_51294 Human_SNP_ID_72788642 A-to-I Human chr2 - 54979181 54979181 54979181 AGCCATGGTCGCCCATGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAAGAGGATTCTTGAGC AGCCATGGTCGCCCATGCCTGTAGTCCCAGCTGCTTGGGAGGCTGAGGCAAGAGGATTCTTGAGC T C RTN4 Ensembl:ENSG00000115310 Protein coding intron GSE107867 ASD brains,cerebellum;ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1375443928 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_330678,RMVar_hsa_circ_265484,RMVar_hsa_circ_199953,RMVar_hsa_circ_273185 51295 RMVar_ID_51295 Human_SNP_ID_72788675 A-to-I Human chr2 - 54979266 54979266 54979266 ATTGCTTGAGGCCAGGAGTTTGAGACCAGCCTAGGCAACATTGTGAGACTGTTTCTATAAAAAAA ATTGCTTGAGGCCAGGAGTTTGAGACCAGCCTGGGCAACATTGTGAGACTGTTTCTATAAAAAAA T C RTN4 Ensembl:ENSG00000115310 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1489214677 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13915579 RMVar_hsa_circ_330678,RMVar_hsa_circ_265484,RMVar_hsa_circ_199953,RMVar_hsa_circ_273185 51296 RMVar_ID_51296 Human_SNP_ID_72788678 A-to-I Human chr2 - 54979285 54979285 54979285 GGGAGGCCAAGGCGGAAGGATTGCTTGAGGCCAGGAGTTTGAGACCAGCCTAGGCAACATTGTGA GGGAGGCCAAGGCGGAAGGATTGCTTGAGGCCGGGAGTTTGAGACCAGCCTAGGCAACATTGTGA T C RTN4 Ensembl:ENSG00000115310 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1214310780 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_330678,RMVar_hsa_circ_265484,RMVar_hsa_circ_199953,RMVar_hsa_circ_273185 51297 RMVar_ID_51297 Human_SNP_ID_72788685 A-to-I Human chr2 - 54979309 54979309 54979309 TCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGAAGGATTGCTTGAGGCCAGGAGTTTG TCACGCCTGTAATCCCAGCACTTTGGGAGGCCTAGGCGGAAGGATTGCTTGAGGCCAGGAGTTTG T A RTN4 Ensembl:ENSG00000115310 Protein coding intron GSE107867 ASD brains,frontal_cortex;ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1411175133 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13915580 RMVar_hsa_circ_330678,RMVar_hsa_circ_265484,RMVar_hsa_circ_199953,RMVar_hsa_circ_273185 51298 RMVar_ID_51298 Human_SNP_ID_72790255 A-to-I Human chr2 - 54984902 54984902 54984902 TGGGTCTCACTGTGTCGCCCAGGCTAGTCTCGAACTCCTGGACTCAAGCAATCCTCCTGCCTCAA TGGGTCTCACTGTGTCGCCCAGGCTAGTCTCGCACTCCTGGACTCAAGCAATCCTCCTGCCTCAA T G RTN4 Ensembl:ENSG00000115310 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs987684878 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_330678,RMVar_hsa_circ_199954,RMVar_hsa_circ_102736,RMVar_hsa_circ_265484,RMVar_hsa_circ_199953,RMVar_hsa_circ_273185,RMVar_hsa_circ_285250,RMVar_hsa_circ_378931,RMVar_hsa_circ_277341,RMVar_hsa_circ_199956,RMVar_hsa_circ_199957,RMVar_hsa_circ_199955 51299 RMVar_ID_51299 Human_SNP_ID_72790260 A-to-I Human chr2 - 54984909 54984909 54984909 AAAGAGATGGGTCTCACTGTGTCGCCCAGGCTAGTCTCGAACTCCTGGACTCAAGCAATCCTCCT AAAGAGATGGGTCTCACTGTGTCGCCCAGGCTTGTCTCGAACTCCTGGACTCAAGCAATCCTCCT T A RTN4 Ensembl:ENSG00000115310 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs935636491 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_330678,RMVar_hsa_circ_199954,RMVar_hsa_circ_102736,RMVar_hsa_circ_265484,RMVar_hsa_circ_199953,RMVar_hsa_circ_273185,RMVar_hsa_circ_285250,RMVar_hsa_circ_378931,RMVar_hsa_circ_277341,RMVar_hsa_circ_199956,RMVar_hsa_circ_199957,RMVar_hsa_circ_199955 51300 RMVar_ID_51300 Human_SNP_ID_72803067 A-to-I Human chr2 - 55032262 55032262 55032262 CCAGCTTGGCCAACGTAGTGAACCCCGTCTCTACTAAAAACACAAAAATTAGCTTGGTGTGATGG CCAGCTTGGCCAACGTAGTGAACCCCGTCTCTTCTAAAAACACAAAAATTAGCTTGGTGTGATGG T A RTN4 Ensembl:ENSG00000115310 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1169228236 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21932026 51301 RMVar_ID_51301 Human_SNP_ID_72803068 A-to-I Human chr2 - 55032262 55032262 55032262 CCAGCTTGGCCAACGTAGTGAACCCCGTCTCTACTAAAAACACAAAAATTAGCTTGGTGTGATGG CCAGCTTGGCCAACGTAGTGAACCCCGTCTCTGCTAAAAACACAAAAATTAGCTTGGTGTGATGG T C RTN4 Ensembl:ENSG00000115310 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1169228236 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21932026 51302 RMVar_ID_51302 Human_SNP_ID_72843882 A-to-I Human chr2 - 55184681 55184681 55184681 AGACTGGTCTCGAACTCCTGACCCTGTGATCCACCTGCATTAGCCTCCCAAAGTGCTGGGATTAC AGACTGGTCTCGAACTCCTGACCCTGTGATCCGCCTGCATTAGCCTCCCAAAGTGCTGGGATTAC T C CLHC1 Ensembl:ENSG00000162994 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1454325906 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13916666,Human_RBP_ID_25550237 RMVar_hsa_circ_290431,RMVar_hsa_circ_326549,RMVar_hsa_circ_331724,RMVar_hsa_circ_309747,RMVar_hsa_circ_68136,RMVar_hsa_circ_267803,RMVar_hsa_circ_56088,RMVar_hsa_circ_69365,RMVar_hsa_circ_199969,RMVar_hsa_circ_199970,RMVar_hsa_circ_199971,RMVar_hsa_circ_354478,RMVar_hsa_circ_199968,RMVar_hsa_circ_327567,RMVar_hsa_circ_38654,RMVar_hsa_circ_38838 51303 RMVar_ID_51303 Human_SNP_ID_72843903 A-to-I Human chr2 - 55184765 55184765 55184765 GAGTAGGTGAGATTAAAGGCAGGTGCCACCACACCTGGCTAATTTTTGTATTTTTAGTAGAGACA GAGTAGGTGAGATTAAAGGCAGGTGCCACCACCCCTGGCTAATTTTTGTATTTTTAGTAGAGACA T G CLHC1 Ensembl:ENSG00000162994 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1047154425 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_290431,RMVar_hsa_circ_326549,RMVar_hsa_circ_331724,RMVar_hsa_circ_309747,RMVar_hsa_circ_68136,RMVar_hsa_circ_267803,RMVar_hsa_circ_56088,RMVar_hsa_circ_69365,RMVar_hsa_circ_199969,RMVar_hsa_circ_199970,RMVar_hsa_circ_199971,RMVar_hsa_circ_354478,RMVar_hsa_circ_199968,RMVar_hsa_circ_327567,RMVar_hsa_circ_38654,RMVar_hsa_circ_38838 51304 RMVar_ID_51304 Human_SNP_ID_72846716 A-to-I Human chr2 - 55195266 55195266 55195266 CACAGAAACACAAATAGTACATGATCTCATTTATATGTGGAATCCAAAAAAGTTGAATTCATAGA CACAGAAACACAAATAGTACATGATCTCATTTGTATGTGGAATCCAAAAAAGTTGAATTCATAGA T C CLHC1 Ensembl:ENSG00000162994 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1313023856 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_290431,RMVar_hsa_circ_326549,RMVar_hsa_circ_331724,RMVar_hsa_circ_309747,RMVar_hsa_circ_68136,RMVar_hsa_circ_267803,RMVar_hsa_circ_56088,RMVar_hsa_circ_69365,RMVar_hsa_circ_199969,RMVar_hsa_circ_199970,RMVar_hsa_circ_199971,RMVar_hsa_circ_354478,RMVar_hsa_circ_199968,RMVar_hsa_circ_327567,RMVar_hsa_circ_38654,RMVar_hsa_circ_38838 51305 RMVar_ID_51305 Human_SNP_ID_72846725 A-to-I Human chr2 - 55195320 55195320 55195320 ATACAACAACATGGATAAACCTGGAGCACATTATACTAAGTGAACTAAGCCAGGCACAGAAACAC ATACAACAACATGGATAAACCTGGAGCACATTGTACTAAGTGAACTAAGCCAGGCACAGAAACAC T C CLHC1 Ensembl:ENSG00000162994 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1181422520 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_290431,RMVar_hsa_circ_326549,RMVar_hsa_circ_331724,RMVar_hsa_circ_309747,RMVar_hsa_circ_68136,RMVar_hsa_circ_267803,RMVar_hsa_circ_56088,RMVar_hsa_circ_69365,RMVar_hsa_circ_199969,RMVar_hsa_circ_199970,RMVar_hsa_circ_199971,RMVar_hsa_circ_354478,RMVar_hsa_circ_199968,RMVar_hsa_circ_327567,RMVar_hsa_circ_38654,RMVar_hsa_circ_38838 51306 RMVar_ID_51306 Human_SNP_ID_72852328 A-to-I Human chr2 - 55215157 55215157 55215157 CATCTCAACATCTGGCCAGTCATATTGCCAGAAATGGAGGTCAAACTTTGCATAGTTTTCCAAGT CATCTCAACATCTGGCCAGTCATATTGCCAGAGATGGAGGTCAAACTTTGCATAGTTTTCCAAGT T C AC012358.1,CLHC1 Ensembl:ENSG00000203327,Ensembl:ENSG00000162994 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947044867 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_290431,RMVar_hsa_circ_331724,RMVar_hsa_circ_267803,RMVar_hsa_circ_14399,RMVar_hsa_circ_199975,RMVar_hsa_circ_34266,RMVar_hsa_circ_354478,RMVar_hsa_circ_327567,RMVar_hsa_circ_38654,RMVar_hsa_circ_303256,RMVar_hsa_circ_303629,RMVar_hsa_circ_290141,RMVar_hsa_circ_199977,RMVar_hsa_circ_281443,RMVar_hsa_circ_199976,RMVar_hsa_circ_199974,RMVar_hsa_circ_199978,RMVar_hsa_circ_39696,RMVar_hsa_circ_329686,RMVar_hsa_circ_3558,RMVar_hsa_circ_347450,RMVar_hsa_circ_366314,RMVar_hsa_circ_322486,RMVar_hsa_circ_25926 51307 RMVar_ID_51307 Human_SNP_ID_72852339 A-to-I Human chr2 - 55215198 55215198 55215198 TAAAAATATATTCTGTAGTACTTTTCTTCAGTAGGAAGGTCCATCTCAACATCTGGCCAGTCATA TAAAAATATATTCTGTAGTACTTTTCTTCAGTGGGAAGGTCCATCTCAACATCTGGCCAGTCATA T C AC012358.1,CLHC1 Ensembl:ENSG00000203327,Ensembl:ENSG00000162994 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1195454062 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_290431,RMVar_hsa_circ_331724,RMVar_hsa_circ_267803,RMVar_hsa_circ_14399,RMVar_hsa_circ_199975,RMVar_hsa_circ_34266,RMVar_hsa_circ_354478,RMVar_hsa_circ_327567,RMVar_hsa_circ_38654,RMVar_hsa_circ_303256,RMVar_hsa_circ_303629,RMVar_hsa_circ_290141,RMVar_hsa_circ_199977,RMVar_hsa_circ_281443,RMVar_hsa_circ_199976,RMVar_hsa_circ_199974,RMVar_hsa_circ_199978,RMVar_hsa_circ_39696,RMVar_hsa_circ_329686,RMVar_hsa_circ_3558,RMVar_hsa_circ_347450,RMVar_hsa_circ_366314,RMVar_hsa_circ_322486,RMVar_hsa_circ_25926 51308 RMVar_ID_51308 Human_SNP_ID_72852346 A-to-I Human chr2 - 55215223 55215223 55215223 TTCTGATGCTTTTGGAAAGATTTTTTAAAAATATATTCTGTAGTACTTTTCTTCAGTAGGAAGGT TTCTGATGCTTTTGGAAAGATTTTTTAAAAATGTATTCTGTAGTACTTTTCTTCAGTAGGAAGGT T C AC012358.1,CLHC1 Ensembl:ENSG00000203327,Ensembl:ENSG00000162994 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1051535365 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13917154 RMVar_hsa_circ_290431,RMVar_hsa_circ_331724,RMVar_hsa_circ_267803,RMVar_hsa_circ_14399,RMVar_hsa_circ_199975,RMVar_hsa_circ_34266,RMVar_hsa_circ_354478,RMVar_hsa_circ_327567,RMVar_hsa_circ_38654,RMVar_hsa_circ_303256,RMVar_hsa_circ_303629,RMVar_hsa_circ_290141,RMVar_hsa_circ_199977,RMVar_hsa_circ_281443,RMVar_hsa_circ_199976,RMVar_hsa_circ_199974,RMVar_hsa_circ_199978,RMVar_hsa_circ_39696,RMVar_hsa_circ_329686,RMVar_hsa_circ_3558,RMVar_hsa_circ_347450,RMVar_hsa_circ_366314,RMVar_hsa_circ_322486,RMVar_hsa_circ_25926 51309 RMVar_ID_51309 Human_SNP_ID_72852525 A-to-I Human chr2 - 55215976 55215976 55215976 GCCACCGTGCCCGGCCTTTTACAGATAATTTTAAGTCAACTTGGAAACTATGCAAAGTTTGACCT GCCACCGTGCCCGGCCTTTTACAGATAATTTTCAGTCAACTTGGAAACTATGCAAAGTTTGACCT T G AC012358.1,CLHC1 Ensembl:ENSG00000203327,Ensembl:ENSG00000162994 lincRNA,Protein coding exon,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs998727559 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6931431,Human_RBP_ID_13917174 Human_Splice_Rec_246587 RMVar_hsa_circ_290431,RMVar_hsa_circ_331724,RMVar_hsa_circ_267803,RMVar_hsa_circ_14399,RMVar_hsa_circ_199975,RMVar_hsa_circ_34266,RMVar_hsa_circ_354478,RMVar_hsa_circ_327567,RMVar_hsa_circ_38654,RMVar_hsa_circ_303256,RMVar_hsa_circ_303629,RMVar_hsa_circ_290141,RMVar_hsa_circ_199977,RMVar_hsa_circ_281443,RMVar_hsa_circ_199976,RMVar_hsa_circ_199974,RMVar_hsa_circ_199978,RMVar_hsa_circ_39696,RMVar_hsa_circ_329686,RMVar_hsa_circ_3558,RMVar_hsa_circ_347450,RMVar_hsa_circ_366314,RMVar_hsa_circ_322486,RMVar_hsa_circ_25926 51310 RMVar_ID_51310 Human_SNP_ID_72853770 A-to-I Human chr2 - 55220016 55220016 55220016 TGGATGACTTACTGGGCTAGGTGTAGTAGCTCATGTCTGTAATCCTAGAACTTTGGGAGGATTGG TGGATGACTTACTGGGCTAGGTGTAGTAGCTCGTGTCTGTAATCCTAGAACTTTGGGAGGATTGG T C CLHC1 Ensembl:ENSG00000162994 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924523233 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13917278 RMVar_hsa_circ_290431,RMVar_hsa_circ_331724,RMVar_hsa_circ_267803,RMVar_hsa_circ_14399,RMVar_hsa_circ_34266,RMVar_hsa_circ_354478,RMVar_hsa_circ_38654,RMVar_hsa_circ_303629,RMVar_hsa_circ_199977,RMVar_hsa_circ_281443,RMVar_hsa_circ_199976,RMVar_hsa_circ_199978,RMVar_hsa_circ_39696,RMVar_hsa_circ_329686,RMVar_hsa_circ_366314,RMVar_hsa_circ_322486 51311 RMVar_ID_51311 Human_SNP_ID_72853771 A-to-I Human chr2 - 55220021 55220021 55220021 AGAAATGGATGACTTACTGGGCTAGGTGTAGTAGCTCATGTCTGTAATCCTAGAACTTTGGGAGG AGAAATGGATGACTTACTGGGCTAGGTGTAGTGGCTCATGTCTGTAATCCTAGAACTTTGGGAGG T C CLHC1 Ensembl:ENSG00000162994 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1399261252 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13917278 RMVar_hsa_circ_290431,RMVar_hsa_circ_331724,RMVar_hsa_circ_267803,RMVar_hsa_circ_14399,RMVar_hsa_circ_34266,RMVar_hsa_circ_354478,RMVar_hsa_circ_38654,RMVar_hsa_circ_303629,RMVar_hsa_circ_199977,RMVar_hsa_circ_281443,RMVar_hsa_circ_199976,RMVar_hsa_circ_199978,RMVar_hsa_circ_39696,RMVar_hsa_circ_329686,RMVar_hsa_circ_366314,RMVar_hsa_circ_322486 51312 RMVar_ID_51312 Human_SNP_ID_72853774 A-to-I Human chr2 - 55220024 55220024 55220024 TTTAGAAATGGATGACTTACTGGGCTAGGTGTAGTAGCTCATGTCTGTAATCCTAGAACTTTGGG TTTAGAAATGGATGACTTACTGGGCTAGGTGTGGTAGCTCATGTCTGTAATCCTAGAACTTTGGG T C CLHC1 Ensembl:ENSG00000162994 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1368546551 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13917278 RMVar_hsa_circ_290431,RMVar_hsa_circ_331724,RMVar_hsa_circ_267803,RMVar_hsa_circ_14399,RMVar_hsa_circ_34266,RMVar_hsa_circ_354478,RMVar_hsa_circ_38654,RMVar_hsa_circ_303629,RMVar_hsa_circ_199977,RMVar_hsa_circ_281443,RMVar_hsa_circ_199976,RMVar_hsa_circ_199978,RMVar_hsa_circ_39696,RMVar_hsa_circ_329686,RMVar_hsa_circ_366314,RMVar_hsa_circ_322486 51313 RMVar_ID_51313 Human_SNP_ID_72854987 A-to-I Human chr2 - 55223919 55223919 55223919 TGGTGGCGGGCGCCTGTAGTCCCAGCTACTCAAGAGGCTGAGGCAGGAGAATCGCGTGAACTCGG TGGTGGCGGGCGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCGCGTGAACTCGG T C CLHC1 Ensembl:ENSG00000162994 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1163719332 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_331724,RMVar_hsa_circ_267803,RMVar_hsa_circ_14399,RMVar_hsa_circ_34266,RMVar_hsa_circ_38654,RMVar_hsa_circ_303629,RMVar_hsa_circ_199977,RMVar_hsa_circ_39696 51314 RMVar_ID_51314 Human_SNP_ID_72855807 A-to-I Human chr2 - 55226724 55226724 55226724 GGGAGGCTAAGGCAGGAGAATCACTTGAATTCAGAAAGTGAAGGTTGCAGTGAGCTGAGATCGTG GGGAGGCTAAGGCAGGAGAATCACTTGAATTCGGAAAGTGAAGGTTGCAGTGAGCTGAGATCGTG T C CLHC1 Ensembl:ENSG00000162994 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1360216461 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13917469 RMVar_hsa_circ_331724,RMVar_hsa_circ_267803,RMVar_hsa_circ_14399,RMVar_hsa_circ_34266,RMVar_hsa_circ_38654,RMVar_hsa_circ_303629,RMVar_hsa_circ_199977,RMVar_hsa_circ_39696 51315 RMVar_ID_51315 Human_SNP_ID_72855810 A-to-I Human chr2 - 55226734 55226734 55226734 TCAGCTACTCGGGAGGCTAAGGCAGGAGAATCACTTGAATTCAGAAAGTGAAGGTTGCAGTGAGC TCAGCTACTCGGGAGGCTAAGGCAGGAGAATCGCTTGAATTCAGAAAGTGAAGGTTGCAGTGAGC T C CLHC1 Ensembl:ENSG00000162994 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1380193248 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13917469 RMVar_hsa_circ_331724,RMVar_hsa_circ_267803,RMVar_hsa_circ_14399,RMVar_hsa_circ_34266,RMVar_hsa_circ_38654,RMVar_hsa_circ_303629,RMVar_hsa_circ_199977,RMVar_hsa_circ_39696 51316 RMVar_ID_51316 Human_SNP_ID_72855823 A-to-I Human chr2 - 55226776 55226776 55226776 TTACAAAAAATTACCCAGACATGGTGCCCTGCACCTCTAGTTTCAGCTACTCGGGAGGCTAAGGC TTACAAAAAATTACCCAGACATGGTGCCCTGCTCCTCTAGTTTCAGCTACTCGGGAGGCTAAGGC T A CLHC1 Ensembl:ENSG00000162994 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886928686 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13917470 RMVar_hsa_circ_331724,RMVar_hsa_circ_267803,RMVar_hsa_circ_14399,RMVar_hsa_circ_34266,RMVar_hsa_circ_38654,RMVar_hsa_circ_303629,RMVar_hsa_circ_199977,RMVar_hsa_circ_39696 51317 RMVar_ID_51317 Human_SNP_ID_72855826 A-to-I Human chr2 - 55226792 55226792 55226792 CCCATCTCTACTAAAATTACAAAAAATTACCCAGACATGGTGCCCTGCACCTCTAGTTTCAGCTA CCCATCTCTACTAAAATTACAAAAAATTACCCCGACATGGTGCCCTGCACCTCTAGTTTCAGCTA T G CLHC1 Ensembl:ENSG00000162994 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs938615305 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_331724,RMVar_hsa_circ_267803,RMVar_hsa_circ_14399,RMVar_hsa_circ_34266,RMVar_hsa_circ_38654,RMVar_hsa_circ_303629,RMVar_hsa_circ_199977,RMVar_hsa_circ_39696 51318 RMVar_ID_51318 Human_SNP_ID_72855851 A-to-I Human chr2 - 55226922 55226922 55226922 TGTTTATATTAGTGAAAATAGCAGCCAGGTGCAGTGGCTCATGCCTGTAATCCCAGCACTTTGGG TGTTTATATTAGTGAAAATAGCAGCCAGGTGCCGTGGCTCATGCCTGTAATCCCAGCACTTTGGG T G CLHC1 Ensembl:ENSG00000162994 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs940551379 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_331724,RMVar_hsa_circ_267803,RMVar_hsa_circ_14399,RMVar_hsa_circ_34266,RMVar_hsa_circ_38654,RMVar_hsa_circ_303629,RMVar_hsa_circ_199977,RMVar_hsa_circ_39696 51319 RMVar_ID_51319 Human_SNP_ID_72862863 A-to-I Human chr2 - 55249841 55249841 55249841 GTGATCCACCCGCCTCAGCTTCCCAAAGTGCTAGGATTACAGGCATGAGCCACCGCACCCAGCCC GTGATCCACCCGCCTCAGCTTCCCAAAGTGCTTGGATTACAGGCATGAGCCACCGCACCCAGCCC T A MTIF2 Ensembl:ENSG00000085760 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1271802530 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20900,RMVar_hsa_circ_22221,RMVar_hsa_circ_104594,RMVar_hsa_circ_199985,RMVar_hsa_circ_34800,RMVar_hsa_circ_51079,RMVar_hsa_circ_60437,RMVar_hsa_circ_89499,RMVar_hsa_circ_199986,RMVar_hsa_circ_16613,RMVar_hsa_circ_50498,RMVar_hsa_circ_315559,RMVar_hsa_circ_342356,RMVar_hsa_circ_310371,RMVar_hsa_circ_38861,RMVar_hsa_circ_199988 51320 RMVar_ID_51320 Human_SNP_ID_72863173 A-to-I Human chr2 - 55251084 55251084 55251084 TTTTTTGAGACGGAGTTTTGCTCTTATTGCCCAGGCTGGAGTGCAGTGGTGCAATCTTGGCTCAC TTTTTTGAGACGGAGTTTTGCTCTTATTGCCCTGGCTGGAGTGCAGTGGTGCAATCTTGGCTCAC T A MTIF2 Ensembl:ENSG00000085760 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1305330892 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20900,RMVar_hsa_circ_22221,RMVar_hsa_circ_104594,RMVar_hsa_circ_199985,RMVar_hsa_circ_34800,RMVar_hsa_circ_51079,RMVar_hsa_circ_60437,RMVar_hsa_circ_89499,RMVar_hsa_circ_199986,RMVar_hsa_circ_16613,RMVar_hsa_circ_50498,RMVar_hsa_circ_315559,RMVar_hsa_circ_342356,RMVar_hsa_circ_310371,RMVar_hsa_circ_38861,RMVar_hsa_circ_199988 51321 RMVar_ID_51321 Human_SNP_ID_72863177 A-to-I Human chr2 - 55251091 55251091 55251091 TTTTTTTTTTTTTGAGACGGAGTTTTGCTCTTATTGCCCAGGCTGGAGTGCAGTGGTGCAATCTT TTTTTTTTTTTTTGAGACGGAGTTTTGCTCTTTTTGCCCAGGCTGGAGTGCAGTGGTGCAATCTT T A MTIF2 Ensembl:ENSG00000085760 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1162413459 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20900,RMVar_hsa_circ_22221,RMVar_hsa_circ_104594,RMVar_hsa_circ_199985,RMVar_hsa_circ_34800,RMVar_hsa_circ_51079,RMVar_hsa_circ_60437,RMVar_hsa_circ_89499,RMVar_hsa_circ_199986,RMVar_hsa_circ_16613,RMVar_hsa_circ_50498,RMVar_hsa_circ_315559,RMVar_hsa_circ_342356,RMVar_hsa_circ_310371,RMVar_hsa_circ_38861,RMVar_hsa_circ_199988 51322 RMVar_ID_51322 Human_SNP_ID_72863352 A-to-I Human chr2 - 55251720 55251720 55251720 ACTTGGGAGGCTGAGGCAGGAGAATCACTTGAACCCGGGAGGTGGAGGTAGTGGTGAGCCGAGAT ACTTGGGAGGCTGAGGCAGGAGAATCACTTGAGCCCGGGAGGTGGAGGTAGTGGTGAGCCGAGAT T C MTIF2 Ensembl:ENSG00000085760 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs543978419 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20900,RMVar_hsa_circ_22221,RMVar_hsa_circ_104594,RMVar_hsa_circ_199985,RMVar_hsa_circ_34800,RMVar_hsa_circ_51079,RMVar_hsa_circ_60437,RMVar_hsa_circ_89499,RMVar_hsa_circ_199986,RMVar_hsa_circ_16613,RMVar_hsa_circ_50498,RMVar_hsa_circ_315559,RMVar_hsa_circ_342356,RMVar_hsa_circ_310371,RMVar_hsa_circ_38861,RMVar_hsa_circ_199988 51323 RMVar_ID_51323 Human_SNP_ID_72864988 A-to-I Human chr2 - 55256757 55256757 55256757 GCTACTGCAGTGAGTTAGGATTGTGCCACTGCACTCTAGCCTGGGCAACAGTGTAAGACCCTGTC GCTACTGCAGTGAGTTAGGATTGTGCCACTGCGCTCTAGCCTGGGCAACAGTGTAAGACCCTGTC T C MTIF2 Ensembl:ENSG00000085760 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs565479381 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20900,RMVar_hsa_circ_34800,RMVar_hsa_circ_51079,RMVar_hsa_circ_89499,RMVar_hsa_circ_199986,RMVar_hsa_circ_16613,RMVar_hsa_circ_50498,RMVar_hsa_circ_315559,RMVar_hsa_circ_310371,RMVar_hsa_circ_199988,RMVar_hsa_circ_357322 51324 RMVar_ID_51324 Human_SNP_ID_72865021 A-to-I Human chr2 - 55256871 55256871 55256871 AAAATGGCAAGAACCCTTCTCTACAAAAAATTAGTAGGATGTAGTGGTGGCACCTGTGGTCCCAG AAAATGGCAAGAACCCTTCTCTACAAAAAATTGGTAGGATGTAGTGGTGGCACCTGTGGTCCCAG T C MTIF2 Ensembl:ENSG00000085760 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs985558713 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_20900,RMVar_hsa_circ_34800,RMVar_hsa_circ_51079,RMVar_hsa_circ_89499,RMVar_hsa_circ_199986,RMVar_hsa_circ_16613,RMVar_hsa_circ_50498,RMVar_hsa_circ_315559,RMVar_hsa_circ_310371,RMVar_hsa_circ_199988,RMVar_hsa_circ_357322 51325 RMVar_ID_51325 Human_SNP_ID_72874006 A-to-I Human chr2 - 55286371 55286371 55286371 CACTGCAGCCTGGACTTCCTAGTAATCCTCCCACTTCAGCCTCCCAAGTAGCCGGGACTACAGGT CACTGCAGCCTGGACTTCCTAGTAATCCTCCCGCTTCAGCCTCCCAAGTAGCCGGGACTACAGGT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1331133704 Functional Loss SNV dbSNP153 33..33 33 - - - 51326 RMVar_ID_51326 Human_SNP_ID_72876800 A-to-I Human chr2 - 55296941 55296941 55296941 TGACCTCGTGATCCGCCTGCTTCGGCCTTCCAAAGTGTTGGGATTACAGGCGTGAGCCACCACGC TGACCTCGTGATCCGCCTGCTTCGGCCTTCCAGAGTGTTGGGATTACAGGCGTGAGCCACCACGC T C CCDC88A Ensembl:ENSG00000115355 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs953085702 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69941,RMVar_hsa_circ_127969,RMVar_hsa_circ_337700,RMVar_hsa_circ_199992,RMVar_hsa_circ_53736,RMVar_hsa_circ_339747,RMVar_hsa_circ_368806,RMVar_hsa_circ_52987,RMVar_hsa_circ_306073,RMVar_hsa_circ_29096,RMVar_hsa_circ_199993,RMVar_hsa_circ_199994,RMVar_hsa_circ_68042,RMVar_hsa_circ_268742 51327 RMVar_ID_51327 Human_SNP_ID_72876842 A-to-I Human chr2 - 55297062 55297062 55297062 CTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTACAGGCGTGCACCAGCACGCCTGGCAAATTTTT CTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTGCAGGCGTGCACCAGCACGCCTGGCAAATTTTT T C CCDC88A Ensembl:ENSG00000115355 Protein coding intron GSE47997;GSE100210;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;HepG2 cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,29129909,31158229 RNA-Seq:(High) rs532886986 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69941,RMVar_hsa_circ_127969,RMVar_hsa_circ_337700,RMVar_hsa_circ_199992,RMVar_hsa_circ_53736,RMVar_hsa_circ_339747,RMVar_hsa_circ_368806,RMVar_hsa_circ_52987,RMVar_hsa_circ_306073,RMVar_hsa_circ_29096,RMVar_hsa_circ_199993,RMVar_hsa_circ_199994,RMVar_hsa_circ_68042,RMVar_hsa_circ_268742 51328 RMVar_ID_51328 Human_SNP_ID_72876848 A-to-I Human chr2 - 55297097 55297097 55297097 CACTGCAACCTCCACCCCCCCAGTATCAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGA CACTGCAACCTCCACCCCCCCAGTATCAAGCAGTTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGA T C CCDC88A Ensembl:ENSG00000115355 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1289990931 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69941,RMVar_hsa_circ_127969,RMVar_hsa_circ_337700,RMVar_hsa_circ_199992,RMVar_hsa_circ_53736,RMVar_hsa_circ_339747,RMVar_hsa_circ_368806,RMVar_hsa_circ_52987,RMVar_hsa_circ_306073,RMVar_hsa_circ_29096,RMVar_hsa_circ_199993,RMVar_hsa_circ_199994,RMVar_hsa_circ_68042,RMVar_hsa_circ_268742 51329 RMVar_ID_51329 Human_SNP_ID_72876875 A-to-I Human chr2 - 55297154 55297154 55297154 TTATTTTTATTGTTGAGACAGAGTCTCAGGCCAGAGTGCAGTGGCGCGATCTCTGCTCACTGCAA TTATTTTTATTGTTGAGACAGAGTCTCAGGCCGGAGTGCAGTGGCGCGATCTCTGCTCACTGCAA T C CCDC88A Ensembl:ENSG00000115355 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1449371187 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569618 RMVar_hsa_circ_69941,RMVar_hsa_circ_127969,RMVar_hsa_circ_337700,RMVar_hsa_circ_199992,RMVar_hsa_circ_53736,RMVar_hsa_circ_339747,RMVar_hsa_circ_368806,RMVar_hsa_circ_52987,RMVar_hsa_circ_306073,RMVar_hsa_circ_29096,RMVar_hsa_circ_199993,RMVar_hsa_circ_199994,RMVar_hsa_circ_68042,RMVar_hsa_circ_268742 51330 RMVar_ID_51330 Human_SNP_ID_72877177 A-to-I Human chr2 - 55297638 55297638 55297638 GTGAGGCCGAGGTGGGCAGATCACCTGAGGTCAGGAGTTACAGACCAACCTGGCCAACATGGTGA GTGAGGCCGAGGTGGGCAGATCACCTGAGGTCGGGAGTTACAGACCAACCTGGCCAACATGGTGA T C CCDC88A Ensembl:ENSG00000115355 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1355951421 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69941,RMVar_hsa_circ_127969,RMVar_hsa_circ_337700,RMVar_hsa_circ_199992,RMVar_hsa_circ_53736,RMVar_hsa_circ_339747,RMVar_hsa_circ_368806,RMVar_hsa_circ_52987,RMVar_hsa_circ_306073,RMVar_hsa_circ_29096,RMVar_hsa_circ_199993,RMVar_hsa_circ_199994,RMVar_hsa_circ_68042,RMVar_hsa_circ_268742 51331 RMVar_ID_51331 Human_SNP_ID_72877191 A-to-I Human chr2 - 55297690 55297690 55297690 ATTCACCTAATGAGCCAGGTGCGGTGGCTCACACCTGTAATCCCAGCACTTTGTGAGGCCGAGGT ATTCACCTAATGAGCCAGGTGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGTGAGGCCGAGGT T C CCDC88A Ensembl:ENSG00000115355 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1236075315 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69941,RMVar_hsa_circ_127969,RMVar_hsa_circ_337700,RMVar_hsa_circ_199992,RMVar_hsa_circ_53736,RMVar_hsa_circ_339747,RMVar_hsa_circ_368806,RMVar_hsa_circ_52987,RMVar_hsa_circ_306073,RMVar_hsa_circ_29096,RMVar_hsa_circ_199993,RMVar_hsa_circ_199994,RMVar_hsa_circ_68042,RMVar_hsa_circ_268742 51332 RMVar_ID_51332 Human_SNP_ID_72877579 A-to-I Human chr2 - 55299103 55299103 55299103 ACCTCCCAGGTTCAAGCCATTCTCCTGTCTCAACCTCCCAAGTAGCTGGAACGGCAGGTGCCAAC ACCTCCCAGGTTCAAGCCATTCTCCTGTCTCATCCTCCCAAGTAGCTGGAACGGCAGGTGCCAAC T A CCDC88A Ensembl:ENSG00000115355 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2589115 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69941,RMVar_hsa_circ_127969,RMVar_hsa_circ_337700,RMVar_hsa_circ_199992,RMVar_hsa_circ_53736,RMVar_hsa_circ_339747,RMVar_hsa_circ_368806,RMVar_hsa_circ_52987,RMVar_hsa_circ_306073,RMVar_hsa_circ_29096,RMVar_hsa_circ_199993,RMVar_hsa_circ_199994,RMVar_hsa_circ_68042,RMVar_hsa_circ_268742 51333 RMVar_ID_51333 Human_SNP_ID_72877580 A-to-I Human chr2 - 55299103 55299103 55299103 ACCTCCCAGGTTCAAGCCATTCTCCTGTCTCAACCTCCCAAGTAGCTGGAACGGCAGGTGCCAAC ACCTCCCAGGTTCAAGCCATTCTCCTGTCTCAGCCTCCCAAGTAGCTGGAACGGCAGGTGCCAAC T C CCDC88A Ensembl:ENSG00000115355 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs2589115 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_69941,RMVar_hsa_circ_127969,RMVar_hsa_circ_337700,RMVar_hsa_circ_199992,RMVar_hsa_circ_53736,RMVar_hsa_circ_339747,RMVar_hsa_circ_368806,RMVar_hsa_circ_52987,RMVar_hsa_circ_306073,RMVar_hsa_circ_29096,RMVar_hsa_circ_199993,RMVar_hsa_circ_199994,RMVar_hsa_circ_68042,RMVar_hsa_circ_268742 51334 RMVar_ID_51334 Human_SNP_ID_72885394 A-to-I Human chr2 - 55330426 55330426 55330426 TCTTGTCACCCAGGTTGGAGTGCAGTGGCACAATCTCGGCTCACTGCAACCTCCGCCTCCGAGGT TCTTGTCACCCAGGTTGGAGTGCAGTGGCACAGTCTCGGCTCACTGCAACCTCCGCCTCCGAGGT T C CCDC88A Ensembl:ENSG00000115355 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs539409585 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127969,RMVar_hsa_circ_199992,RMVar_hsa_circ_52987,RMVar_hsa_circ_29096,RMVar_hsa_circ_268742,RMVar_hsa_circ_11747,RMVar_hsa_circ_287618,RMVar_hsa_circ_6495,RMVar_hsa_circ_22193,RMVar_hsa_circ_44179,RMVar_hsa_circ_200002,RMVar_hsa_circ_49140,RMVar_hsa_circ_53621,RMVar_hsa_circ_59398,RMVar_hsa_circ_200010,RMVar_hsa_circ_118927,RMVar_hsa_circ_200013,RMVar_hsa_circ_91935,RMVar_hsa_circ_28369,RMVar_hsa_circ_30247,RMVar_hsa_circ_200015,RMVar_hsa_circ_200014,RMVar_hsa_circ_31707,RMVar_hsa_circ_12626 51335 RMVar_ID_51335 Human_SNP_ID_72896207 A-to-I Human chr2 - 55371781 55371781 55371781 AGAAGGTACTGTTAATAATTATAGAGTGGGCTAGGCGTGGTGGCTCATGCCTGTAATCCCAACAC AGAAGGTACTGTTAATAATTATAGAGTGGGCTCGGCGTGGTGGCTCATGCCTGTAATCCCAACAC T G CCDC88A Ensembl:ENSG00000115355 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1558761049 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13918460 RMVar_hsa_circ_127969,RMVar_hsa_circ_199992,RMVar_hsa_circ_11747,RMVar_hsa_circ_287618,RMVar_hsa_circ_6495,RMVar_hsa_circ_200002,RMVar_hsa_circ_49140,RMVar_hsa_circ_53621,RMVar_hsa_circ_200010,RMVar_hsa_circ_28369,RMVar_hsa_circ_362022,RMVar_hsa_circ_298232,RMVar_hsa_circ_200021,RMVar_hsa_circ_200020,RMVar_hsa_circ_326222,RMVar_hsa_circ_200026,RMVar_hsa_circ_200037,RMVar_hsa_circ_44748,RMVar_hsa_circ_200031,RMVar_hsa_circ_200034,RMVar_hsa_circ_331214,RMVar_hsa_circ_298992,RMVar_hsa_circ_200035,RMVar_hsa_circ_265782,RMVar_hsa_circ_284525,RMVar_hsa_circ_307926,RMVar_hsa_circ_49228,RMVar_hsa_circ_200041,RMVar_hsa_circ_308439,RMVar_hsa_circ_200036,RMVar_hsa_circ_297493,RMVar_hsa_circ_200042,RMVar_hsa_circ_320418 51336 RMVar_ID_51336 Human_SNP_ID_72899704 A-to-I Human chr2 - 55383501 55383501 55383501 CTCCTGCCTCGGCTTCCTGAGTAGCTGGGATTACAGGCACCTGCCACCACACCTGGCTAATTTTT CTCCTGCCTCGGCTTCCTGAGTAGCTGGGATTTCAGGCACCTGCCACCACACCTGGCTAATTTTT T A CCDC88A Ensembl:ENSG00000115355 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1240287932 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_287618,RMVar_hsa_circ_200002,RMVar_hsa_circ_200010,RMVar_hsa_circ_298232,RMVar_hsa_circ_200021,RMVar_hsa_circ_326222,RMVar_hsa_circ_200026,RMVar_hsa_circ_44748,RMVar_hsa_circ_200031,RMVar_hsa_circ_298992,RMVar_hsa_circ_200035,RMVar_hsa_circ_265782,RMVar_hsa_circ_284525,RMVar_hsa_circ_200036,RMVar_hsa_circ_297493,RMVar_hsa_circ_200042,RMVar_hsa_circ_320418,RMVar_hsa_circ_285878,RMVar_hsa_circ_200044 51337 RMVar_ID_51337 Human_SNP_ID_72899705 A-to-I Human chr2 - 55383501 55383501 55383501 CTCCTGCCTCGGCTTCCTGAGTAGCTGGGATTACAGGCACCTGCCACCACACCTGGCTAATTTTT CTCCTGCCTCGGCTTCCTGAGTAGCTGGGATTGCAGGCACCTGCCACCACACCTGGCTAATTTTT T C CCDC88A Ensembl:ENSG00000115355 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1240287932 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_287618,RMVar_hsa_circ_200002,RMVar_hsa_circ_200010,RMVar_hsa_circ_298232,RMVar_hsa_circ_200021,RMVar_hsa_circ_326222,RMVar_hsa_circ_200026,RMVar_hsa_circ_44748,RMVar_hsa_circ_200031,RMVar_hsa_circ_298992,RMVar_hsa_circ_200035,RMVar_hsa_circ_265782,RMVar_hsa_circ_284525,RMVar_hsa_circ_200036,RMVar_hsa_circ_297493,RMVar_hsa_circ_200042,RMVar_hsa_circ_320418,RMVar_hsa_circ_285878,RMVar_hsa_circ_200044 51338 RMVar_ID_51338 Human_SNP_ID_72907181 A-to-I Human chr2 - 55407386 55407386 55407386 TGGCCAGGCGGGTCTCGAACTCCTGACATCAAATGATGCACCTGCCTCAGTCTCCCAAAGTGCTG TGGCCAGGCGGGTCTCGAACTCCTGACATCAATTGATGCACCTGCCTCAGTCTCCCAAAGTGCTG T A CCDC88A Ensembl:ENSG00000115355 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs997105515 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265782,RMVar_hsa_circ_200045,RMVar_hsa_circ_104818 51339 RMVar_ID_51339 Human_SNP_ID_72907182 A-to-I Human chr2 - 55407386 55407386 55407386 TGGCCAGGCGGGTCTCGAACTCCTGACATCAAATGATGCACCTGCCTCAGTCTCCCAAAGTGCTG TGGCCAGGCGGGTCTCGAACTCCTGACATCAAGTGATGCACCTGCCTCAGTCTCCCAAAGTGCTG T C CCDC88A Ensembl:ENSG00000115355 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs997105515 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265782,RMVar_hsa_circ_200045,RMVar_hsa_circ_104818 51340 RMVar_ID_51340 Human_SNP_ID_72943234 A-to-I Human chr2 + 55529746 55529746 55529746 TCGGCTTACTGCATGCTCTGCCTTGCGGGTTTACACCATTCTCCTGCCTCAGCCTTCTGAGTAGC TCGGCTTACTGCATGCTCTGCCTTGCGGGTTTGCACCATTCTCCTGCCTCAGCCTTCTGAGTAGC A G CFAP36 Ensembl:ENSG00000163001 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1378657725 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67793 51341 RMVar_ID_51341 Human_SNP_ID_72943236 A-to-I Human chr2 + 55529748 55529748 55529748 GGCTTACTGCATGCTCTGCCTTGCGGGTTTACACCATTCTCCTGCCTCAGCCTTCTGAGTAGCTG GGCTTACTGCATGCTCTGCCTTGCGGGTTTACCCCATTCTCCTGCCTCAGCCTTCTGAGTAGCTG A C CFAP36 Ensembl:ENSG00000163001 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs377160251 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67793 51342 RMVar_ID_51342 Human_SNP_ID_72944986 A-to-I Human chr2 + 55536514 55536514 55536514 ACTCTGACACCTGGGCTGGAGTGCAGTGGCGCAATCTCGGCTCACTGCAACCTCTGCTTCCCAGG ACTCTGACACCTGGGCTGGAGTGCAGTGGCGCCATCTCGGCTCACTGCAACCTCTGCTTCCCAGG A C CFAP36 Ensembl:ENSG00000163001 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs995306806 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_331031 51343 RMVar_ID_51343 Human_SNP_ID_72944987 A-to-I Human chr2 + 55536514 55536514 55536514 ACTCTGACACCTGGGCTGGAGTGCAGTGGCGCAATCTCGGCTCACTGCAACCTCTGCTTCCCAGG ACTCTGACACCTGGGCTGGAGTGCAGTGGCGCGATCTCGGCTCACTGCAACCTCTGCTTCCCAGG A G CFAP36 Ensembl:ENSG00000163001 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs995306806 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_331031 51344 RMVar_ID_51344 Human_SNP_ID_72945062 A-to-I Human chr2 + 55536793 55536793 55536793 TTGAGACTGAGTCTTGTTGTATTGCCCAGGCTAGAGTGCAGTGGCGTGATCTTGGCTCACTGCAA TTGAGACTGAGTCTTGTTGTATTGCCCAGGCTGGAGTGCAGTGGCGTGATCTTGGCTCACTGCAA A G CFAP36 Ensembl:ENSG00000163001 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1272709501 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_331031 51345 RMVar_ID_51345 Human_SNP_ID_72945065 A-to-I Human chr2 + 55536809 55536809 55536809 TTGTATTGCCCAGGCTAGAGTGCAGTGGCGTGATCTTGGCTCACTGCAACCTCTGCCTCCCAGGC TTGTATTGCCCAGGCTAGAGTGCAGTGGCGTGCTCTTGGCTCACTGCAACCTCTGCCTCCCAGGC A C CFAP36 Ensembl:ENSG00000163001 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1003230214 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_331031 51346 RMVar_ID_51346 Human_SNP_ID_72945066 A-to-I Human chr2 + 55536809 55536809 55536809 TTGTATTGCCCAGGCTAGAGTGCAGTGGCGTGATCTTGGCTCACTGCAACCTCTGCCTCCCAGGC TTGTATTGCCCAGGCTAGAGTGCAGTGGCGTGGTCTTGGCTCACTGCAACCTCTGCCTCCCAGGC A G CFAP36 Ensembl:ENSG00000163001 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1003230214 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_331031 51347 RMVar_ID_51347 Human_SNP_ID_72945155 A-to-I Human chr2 + 55537121 55537121 55537121 TAAAGAGGCCAGACGTGGTGGCTCACTCCTGTAATCCCAGCACTTTGAGAGGCTGAGGTGGGTGG TAAAGAGGCCAGACGTGGTGGCTCACTCCTGTGATCCCAGCACTTTGAGAGGCTGAGGTGGGTGG A G CFAP36 Ensembl:ENSG00000163001 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1247397670 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_331031 51348 RMVar_ID_51348 Human_SNP_ID_72945181 A-to-I Human chr2 + 55537229 55537229 55537229 CCCATCTCTACTAAAAATGCAACAATTAGCCGAGCGTGGTAGTGCACACCTGTAATCCCAGCTAC CCCATCTCTACTAAAAATGCAACAATTAGCCGGGCGTGGTAGTGCACACCTGTAATCCCAGCTAC A G CFAP36 Ensembl:ENSG00000163001 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1213325175 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_331031 51349 RMVar_ID_51349 Human_SNP_ID_72945187 A-to-I Human chr2 + 55537250 55537250 55537250 ACAATTAGCCGAGCGTGGTAGTGCACACCTGTAATCCCAGCTACTCAGGTGGCTCAGGCATGAGA ACAATTAGCCGAGCGTGGTAGTGCACACCTGTGATCCCAGCTACTCAGGTGGCTCAGGCATGAGA A G CFAP36 Ensembl:ENSG00000163001 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs938650826 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_331031 51350 RMVar_ID_51350 Human_SNP_ID_72946902 A-to-I Human chr2 + 55543985 55543985 55543985 TTGCTAATCAGTCAATAGAACCTTTGGGAAGAAAAGTGGAAAGGTCTGAAACTTCCTCCCTCCCA TTGCTAATCAGTCAATAGAACCTTTGGGAAGAGAAGTGGAAAGGTCTGAAACTTCCTCCCTCCCA A G CFAP36 Ensembl:ENSG00000163001 Protein coding CDS GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs150639486 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_552588,Human_RBP_ID_17276408,Human_RBP_ID_17507984,Human_RBP_ID_26339345,Human_RBP_ID_27817134 Human_Splice_Rec_248592,Human_Splice_Rec_248593,Human_Splice_Rec_248624,Human_Splice_Rec_248625,Human_Splice_Rec_248643,Human_Splice_Rec_248664,Human_Splice_Rec_248665 51351 RMVar_ID_51351 Human_SNP_ID_72947992 A-to-I Human chr2 - 55547719 55547719 55547719 CGGGGTTTCACCATCTTGGCCAGGCTGGTCTTAAACTCCTGACCTCACAATCCACCCGCCTCAGC CGGGGTTTCACCATCTTGGCCAGGCTGGTCTTCAACTCCTGACCTCACAATCCACCCGCCTCAGC T G PPP4R3B Ensembl:ENSG00000275052 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1039325220 Functional Loss SNV dbSNP153 33..33 33 - - - 51352 RMVar_ID_51352 Human_SNP_ID_72949112 A-to-I Human chr2 - 55552522 55552522 55552522 AGGCATGGTGGTGCATGCATGTAGCCCAAGCTACTTGGGTGGCTGAGGCACAGGAATCGCTTGCA AGGCATGGTGGTGCATGCATGTAGCCCAAGCTGCTTGGGTGGCTGAGGCACAGGAATCGCTTGCA T C PPP4R3B Ensembl:ENSG00000275052 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1308751731 Functional Loss SNV dbSNP153 33..33 33 - - - 51353 RMVar_ID_51353 Human_SNP_ID_72949124 A-to-I Human chr2 - 55552564 55552564 55552564 CATGGTGAAACCCCATCTCTACTAAAAATACAAAAGTTAGCCAGGCATGGTGGTGCATGCATGTA CATGGTGAAACCCCATCTCTACTAAAAATACAGAAGTTAGCCAGGCATGGTGGTGCATGCATGTA T C PPP4R3B Ensembl:ENSG00000275052 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1221302103 Functional Loss SNV dbSNP153 33..33 33 - - - 51354 RMVar_ID_51354 Human_SNP_ID_72949127 A-to-I Human chr2 - 55552582 55552582 55552582 CAAGGCCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAGTTAGCCAGGCA CAAGGCCAGCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAGTTAGCCAGGCA T C PPP4R3B Ensembl:ENSG00000275052 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs866569396 Functional Loss SNV dbSNP153 33..33 33 - - - 51355 RMVar_ID_51355 Human_SNP_ID_72949529 A-to-I Human chr2 - 55554138 55554138 55554138 ATCACTTGAGCCCAGCGGGCAGAGGTTGCAATAAGCCGAGATCACATCACTGCACTTTCGAGTCT ATCACTTGAGCCCAGCGGGCAGAGGTTGCAATGAGCCGAGATCACATCACTGCACTTTCGAGTCT T C PPP4R3B Ensembl:ENSG00000275052 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs368241705 Functional Loss SNV dbSNP153 33..33 33 - - - 51356 RMVar_ID_51356 Human_SNP_ID_72950295 A-to-I Human chr2 - 55556933 55556933 55556933 TCAGCCTCCCGAGTAGCTGGGAGTGCTGGCGCATGCCACTATGCCTGGCTAATTTTTCTATTTTT TCAGCCTCCCGAGTAGCTGGGAGTGCTGGCGCTTGCCACTATGCCTGGCTAATTTTTCTATTTTT T A PPP4R3B Ensembl:ENSG00000275052 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs568683543 Functional Loss SNV dbSNP153 33..33 33 - - - 51357 RMVar_ID_51357 Human_SNP_ID_72950296 A-to-I Human chr2 - 55556933 55556933 55556933 TCAGCCTCCCGAGTAGCTGGGAGTGCTGGCGCATGCCACTATGCCTGGCTAATTTTTCTATTTTT TCAGCCTCCCGAGTAGCTGGGAGTGCTGGCGCGTGCCACTATGCCTGGCTAATTTTTCTATTTTT T C PPP4R3B Ensembl:ENSG00000275052 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs568683543 Functional Loss SNV dbSNP153 33..33 33 - - - 51358 RMVar_ID_51358 Human_SNP_ID_72950452 A-to-I Human chr2 - 55557412 55557412 55557412 AAGGCAGGAGGATCGCTTGAGCGCAGGAGTCCAAGACCAGTCTGGGCAACAAGGTGAGACCCCAT AAGGCAGGAGGATCGCTTGAGCGCAGGAGTCCGAGACCAGTCTGGGCAACAAGGTGAGACCCCAT T C PPP4R3B Ensembl:ENSG00000275052 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1438653443 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25589888 51359 RMVar_ID_51359 Human_SNP_ID_72954220 A-to-I Human chr2 - 55570087 55570087 55570087 TGCCAGCACACCTGGCTAATTTTTTGTATTTTAGTAAAGACGGGGTTTCACCATGTTGGCCAGGC TGCCAGCACACCTGGCTAATTTTTTGTATTTTGGTAAAGACGGGGTTTCACCATGTTGGCCAGGC T C PPP4R3B Ensembl:ENSG00000275052 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1373309321 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23809,RMVar_hsa_circ_49979,RMVar_hsa_circ_307270,RMVar_hsa_circ_319820,RMVar_hsa_circ_361942,RMVar_hsa_circ_310276,RMVar_hsa_circ_279288,RMVar_hsa_circ_285629,RMVar_hsa_circ_63455,RMVar_hsa_circ_200055,RMVar_hsa_circ_200057,RMVar_hsa_circ_200058,RMVar_hsa_circ_200056,RMVar_hsa_circ_200053,RMVar_hsa_circ_200054,RMVar_hsa_circ_75398,RMVar_hsa_circ_326045,RMVar_hsa_circ_352835,RMVar_hsa_circ_324258,RMVar_hsa_circ_55713,RMVar_hsa_circ_34432,RMVar_hsa_circ_200059,RMVar_hsa_circ_200060,RMVar_hsa_circ_357217,RMVar_hsa_circ_200062,RMVar_hsa_circ_370313,RMVar_hsa_circ_309592,RMVar_hsa_circ_200063,RMVar_hsa_circ_200064 51360 RMVar_ID_51360 Human_SNP_ID_72954547 A-to-I Human chr2 - 55571227 55571227 55571227 CAGCTCACTGCAGCTTCTGCTTCCCGGTTTCAAGTGATTCTCCTGCCTCAGCCTTTCGAGTAGCT CAGCTCACTGCAGCTTCTGCTTCCCGGTTTCAGGTGATTCTCCTGCCTCAGCCTTTCGAGTAGCT T C PPP4R3B Ensembl:ENSG00000275052 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs887208221 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23809,RMVar_hsa_circ_49979,RMVar_hsa_circ_307270,RMVar_hsa_circ_319820,RMVar_hsa_circ_361942,RMVar_hsa_circ_310276,RMVar_hsa_circ_279288,RMVar_hsa_circ_285629,RMVar_hsa_circ_63455,RMVar_hsa_circ_200055,RMVar_hsa_circ_200057,RMVar_hsa_circ_200058,RMVar_hsa_circ_200056,RMVar_hsa_circ_200053,RMVar_hsa_circ_200054,RMVar_hsa_circ_75398,RMVar_hsa_circ_326045,RMVar_hsa_circ_352835,RMVar_hsa_circ_324258,RMVar_hsa_circ_55713,RMVar_hsa_circ_34432,RMVar_hsa_circ_200059,RMVar_hsa_circ_200060,RMVar_hsa_circ_357217,RMVar_hsa_circ_200062,RMVar_hsa_circ_370313,RMVar_hsa_circ_309592,RMVar_hsa_circ_200063,RMVar_hsa_circ_200064 51361 RMVar_ID_51361 Human_SNP_ID_72955598 A-to-I Human chr2 - 55574883 55574883 55574883 ATTAAATCATGTTTAAGAATCAGGCTGGGCGCAGTGGCTTACGCCTGTAATGCCAGCACTTTGGG ATTAAATCATGTTTAAGAATCAGGCTGGGCGCTGTGGCTTACGCCTGTAATGCCAGCACTTTGGG T A PPP4R3B Ensembl:ENSG00000275052 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1053357997 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13919577 RMVar_hsa_circ_23809,RMVar_hsa_circ_49979,RMVar_hsa_circ_307270,RMVar_hsa_circ_319820,RMVar_hsa_circ_361942,RMVar_hsa_circ_310276,RMVar_hsa_circ_279288,RMVar_hsa_circ_63455,RMVar_hsa_circ_200055,RMVar_hsa_circ_200057,RMVar_hsa_circ_200058,RMVar_hsa_circ_200056,RMVar_hsa_circ_200054,RMVar_hsa_circ_75398,RMVar_hsa_circ_326045,RMVar_hsa_circ_352835,RMVar_hsa_circ_55713,RMVar_hsa_circ_54897,RMVar_hsa_circ_34432,RMVar_hsa_circ_200059,RMVar_hsa_circ_357217,RMVar_hsa_circ_200062,RMVar_hsa_circ_370313,RMVar_hsa_circ_309592,RMVar_hsa_circ_200063,RMVar_hsa_circ_200064,RMVar_hsa_circ_344697,RMVar_hsa_circ_364948,RMVar_hsa_circ_200065,RMVar_hsa_circ_200066 51362 RMVar_ID_51362 Human_SNP_ID_72955820 A-to-I Human chr2 - 55575506 55575506 55575506 GGGAGGTTGAGGCTGCATTGAGCCGAAATTGCACCAGTGCCCTCCAGCCTGGGTGACATAGTGAT GGGAGGTTGAGGCTGCATTGAGCCGAAATTGCTCCAGTGCCCTCCAGCCTGGGTGACATAGTGAT T A PPP4R3B Ensembl:ENSG00000275052 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1450410914 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17569621 RMVar_hsa_circ_23809,RMVar_hsa_circ_49979,RMVar_hsa_circ_307270,RMVar_hsa_circ_319820,RMVar_hsa_circ_361942,RMVar_hsa_circ_310276,RMVar_hsa_circ_279288,RMVar_hsa_circ_63455,RMVar_hsa_circ_200055,RMVar_hsa_circ_200057,RMVar_hsa_circ_200058,RMVar_hsa_circ_200056,RMVar_hsa_circ_200054,RMVar_hsa_circ_75398,RMVar_hsa_circ_326045,RMVar_hsa_circ_352835,RMVar_hsa_circ_55713,RMVar_hsa_circ_54897,RMVar_hsa_circ_34432,RMVar_hsa_circ_200059,RMVar_hsa_circ_357217,RMVar_hsa_circ_200062,RMVar_hsa_circ_370313,RMVar_hsa_circ_309592,RMVar_hsa_circ_200063,RMVar_hsa_circ_200064,RMVar_hsa_circ_344697,RMVar_hsa_circ_364948,RMVar_hsa_circ_200065,RMVar_hsa_circ_200066 51363 RMVar_ID_51363 Human_SNP_ID_72956024 A-to-I Human chr2 - 55576265 55576265 55576265 CGGCTCACTGCAACCTCCACCTTCTGGGTTCAAACCATCTCCCGCCTCAGCCTCCCAAGTAGCTG CGGCTCACTGCAACCTCCACCTTCTGGGTTCAGACCATCTCCCGCCTCAGCCTCCCAAGTAGCTG T C PPP4R3B Ensembl:ENSG00000275052 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1310145836 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23809,RMVar_hsa_circ_49979,RMVar_hsa_circ_307270,RMVar_hsa_circ_319820,RMVar_hsa_circ_361942,RMVar_hsa_circ_310276,RMVar_hsa_circ_279288,RMVar_hsa_circ_63455,RMVar_hsa_circ_200055,RMVar_hsa_circ_200057,RMVar_hsa_circ_200058,RMVar_hsa_circ_200056,RMVar_hsa_circ_200054,RMVar_hsa_circ_75398,RMVar_hsa_circ_326045,RMVar_hsa_circ_352835,RMVar_hsa_circ_55713,RMVar_hsa_circ_54897,RMVar_hsa_circ_34432,RMVar_hsa_circ_200059,RMVar_hsa_circ_357217,RMVar_hsa_circ_200062,RMVar_hsa_circ_370313,RMVar_hsa_circ_309592,RMVar_hsa_circ_200063,RMVar_hsa_circ_200064,RMVar_hsa_circ_344697,RMVar_hsa_circ_364948,RMVar_hsa_circ_200065,RMVar_hsa_circ_200066 51364 RMVar_ID_51364 Human_SNP_ID_72956036 A-to-I Human chr2 - 55576317 55576317 55576317 TTGAGACAGAGTCTCACTCTGTCACCCAGGCTAGAGTGCAGTGGCACAATTTCGGCTCACTGCAA TTGAGACAGAGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGCACAATTTCGGCTCACTGCAA T C PPP4R3B Ensembl:ENSG00000275052 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1241598727 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23809,RMVar_hsa_circ_49979,RMVar_hsa_circ_307270,RMVar_hsa_circ_319820,RMVar_hsa_circ_361942,RMVar_hsa_circ_310276,RMVar_hsa_circ_279288,RMVar_hsa_circ_63455,RMVar_hsa_circ_200055,RMVar_hsa_circ_200057,RMVar_hsa_circ_200058,RMVar_hsa_circ_200056,RMVar_hsa_circ_200054,RMVar_hsa_circ_75398,RMVar_hsa_circ_326045,RMVar_hsa_circ_352835,RMVar_hsa_circ_55713,RMVar_hsa_circ_54897,RMVar_hsa_circ_34432,RMVar_hsa_circ_200059,RMVar_hsa_circ_357217,RMVar_hsa_circ_200062,RMVar_hsa_circ_370313,RMVar_hsa_circ_309592,RMVar_hsa_circ_200063,RMVar_hsa_circ_200064,RMVar_hsa_circ_344697,RMVar_hsa_circ_364948,RMVar_hsa_circ_200065,RMVar_hsa_circ_200066 51365 RMVar_ID_51365 Human_SNP_ID_72956163 A-to-I Human chr2 - 55576639 55576639 55576639 GGAGTGCAGTGGCACAATCTCGGCTCACTGCAAGCTCCGCCTCCTGAGTTCAAGCGATTCTTCTG GGAGTGCAGTGGCACAATCTCGGCTCACTGCAGGCTCCGCCTCCTGAGTTCAAGCGATTCTTCTG T C PPP4R3B Ensembl:ENSG00000275052 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1031330013 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_23809,RMVar_hsa_circ_49979,RMVar_hsa_circ_307270,RMVar_hsa_circ_319820,RMVar_hsa_circ_361942,RMVar_hsa_circ_310276,RMVar_hsa_circ_279288,RMVar_hsa_circ_63455,RMVar_hsa_circ_200055,RMVar_hsa_circ_200057,RMVar_hsa_circ_200058,RMVar_hsa_circ_200056,RMVar_hsa_circ_200054,RMVar_hsa_circ_75398,RMVar_hsa_circ_326045,RMVar_hsa_circ_352835,RMVar_hsa_circ_55713,RMVar_hsa_circ_54897,RMVar_hsa_circ_34432,RMVar_hsa_circ_200059,RMVar_hsa_circ_357217,RMVar_hsa_circ_200062,RMVar_hsa_circ_370313,RMVar_hsa_circ_309592,RMVar_hsa_circ_200063,RMVar_hsa_circ_200064,RMVar_hsa_circ_344697,RMVar_hsa_circ_364948,RMVar_hsa_circ_200065,RMVar_hsa_circ_200066 51366 RMVar_ID_51366 Human_SNP_ID_72956683 A-to-I Human chr2 - 55578329 55578329 55578329 TTGCCATATTTTTTTTCAGATTTTTTTTTAAAACATTACAGATATAGTTGGAGTTTCATATGTAC TTGCCATATTTTTTTTCAGATTTTTTTTTAAACCATTACAGATATAGTTGGAGTTTCATATGTAC T G PPP4R3B Ensembl:ENSG00000275052 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1178670278 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_60647,Human_RBP_ID_6932225,Human_RBP_ID_13919672,Human_RBP_ID_25551113 Human_Splice_Rec_248710,Human_Splice_Rec_248711 RMVar_hsa_circ_23809,RMVar_hsa_circ_49979,RMVar_hsa_circ_307270,RMVar_hsa_circ_319820,RMVar_hsa_circ_361942,RMVar_hsa_circ_310276,RMVar_hsa_circ_279288,RMVar_hsa_circ_200055,RMVar_hsa_circ_200057,RMVar_hsa_circ_200058,RMVar_hsa_circ_200056,RMVar_hsa_circ_200054,RMVar_hsa_circ_75398,RMVar_hsa_circ_326045,RMVar_hsa_circ_352835,RMVar_hsa_circ_55713,RMVar_hsa_circ_200067,RMVar_hsa_circ_54897,RMVar_hsa_circ_200059,RMVar_hsa_circ_357217,RMVar_hsa_circ_200062,RMVar_hsa_circ_370313,RMVar_hsa_circ_309592,RMVar_hsa_circ_200064,RMVar_hsa_circ_344697,RMVar_hsa_circ_364948,RMVar_hsa_circ_200065,RMVar_hsa_circ_200066,RMVar_hsa_circ_200069,RMVar_hsa_circ_308230,RMVar_hsa_circ_374660,RMVar_hsa_circ_280886,RMVar_hsa_circ_200068,RMVar_hsa_circ_60986 51367 RMVar_ID_51367 Human_SNP_ID_72961689 A-to-I Human chr2 - 55595297 55595297 55595297 GTTTAGGCTGGGTGTGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCCAGGAGG GTTTAGGCTGGGTGTGGTGGCTCATGCCTGTAGTCCCAGCACTTTGGGAGGCCAAGGCCAGGAGG T C PPP4R3B Ensembl:ENSG00000275052 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1197510054 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_307270,RMVar_hsa_circ_319820,RMVar_hsa_circ_200057,RMVar_hsa_circ_200058,RMVar_hsa_circ_55713,RMVar_hsa_circ_44951,RMVar_hsa_circ_54897,RMVar_hsa_circ_200066,RMVar_hsa_circ_341092,RMVar_hsa_circ_60585,RMVar_hsa_circ_200070,RMVar_hsa_circ_344388,RMVar_hsa_circ_200076,RMVar_hsa_circ_67892,RMVar_hsa_circ_318917 51368 RMVar_ID_51368 Human_SNP_ID_72961710 A-to-I Human chr2 - 55595373 55595373 55595373 GATGCTCCTCACCCTCCCAAAGTGCTGAGATTATAGATATGAGCCACTGTACCCAGCCTCTGCAT GATGCTCCTCACCCTCCCAAAGTGCTGAGATTGTAGATATGAGCCACTGTACCCAGCCTCTGCAT T C PPP4R3B Ensembl:ENSG00000275052 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1470371718 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_307270,RMVar_hsa_circ_319820,RMVar_hsa_circ_200057,RMVar_hsa_circ_200058,RMVar_hsa_circ_55713,RMVar_hsa_circ_44951,RMVar_hsa_circ_54897,RMVar_hsa_circ_200066,RMVar_hsa_circ_341092,RMVar_hsa_circ_60585,RMVar_hsa_circ_200070,RMVar_hsa_circ_344388,RMVar_hsa_circ_200076,RMVar_hsa_circ_67892,RMVar_hsa_circ_318917 51369 RMVar_ID_51369 Human_SNP_ID_72962648 A-to-I Human chr2 - 55598173 55598173 55598173 TTCTGTCGCCCAGGCTGGAATGCAGTGGCGCAATCTCAGCTCACTGCAACCTACGCTTCCCGGGT TTCTGTCGCCCAGGCTGGAATGCAGTGGCGCAGTCTCAGCTCACTGCAACCTACGCTTCCCGGGT T C PPP4R3B Ensembl:ENSG00000275052 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs905327720 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_307270,RMVar_hsa_circ_319820,RMVar_hsa_circ_200057,RMVar_hsa_circ_200058,RMVar_hsa_circ_55713,RMVar_hsa_circ_44951,RMVar_hsa_circ_54897,RMVar_hsa_circ_200066,RMVar_hsa_circ_341092,RMVar_hsa_circ_60585,RMVar_hsa_circ_200070,RMVar_hsa_circ_344388,RMVar_hsa_circ_200076,RMVar_hsa_circ_67892,RMVar_hsa_circ_318917 51370 RMVar_ID_51370 Human_SNP_ID_72966726 A-to-I Human chr2 - 55611128 55611128 55611128 ACTAGGCACAGTGGCTCACACTTGTAATCTCAACACTTTGGGAGGCTGAGGCAGGAGGATCACTT ACTAGGCACAGTGGCTCACACTTGTAATCTCACCACTTTGGGAGGCTGAGGCAGGAGGATCACTT T G PPP4R3B Ensembl:ENSG00000275052 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1186365717 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_307270,RMVar_hsa_circ_200058,RMVar_hsa_circ_67892,RMVar_hsa_circ_367484,RMVar_hsa_circ_310655 51371 RMVar_ID_51371 Human_SNP_ID_72966784 A-to-I Human chr2 - 55611294 55611294 55611294 AGCCAGGTGTGGTGGCGTGTGCTTGTGGTCCCAGCTCCTTGGGAGGCTGAGGCTGGAGGATCACT AGCCAGGTGTGGTGGCGTGTGCTTGTGGTCCCGGCTCCTTGGGAGGCTGAGGCTGGAGGATCACT T C PPP4R3B Ensembl:ENSG00000275052 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs541430715 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_307270,RMVar_hsa_circ_200058,RMVar_hsa_circ_67892,RMVar_hsa_circ_367484,RMVar_hsa_circ_310655 51372 RMVar_ID_51372 Human_SNP_ID_72967009 A-to-I Human chr2 - 55612005 55612005 55612005 GACTATGGCAGGCATGGTGGCTCACACCTGCAATCTCAGCACTTTGGAAGGCCAAGGCAGGAGGA GACTATGGCAGGCATGGTGGCTCACACCTGCAGTCTCAGCACTTTGGAAGGCCAAGGCAGGAGGA T C PPP4R3B Ensembl:ENSG00000275052 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903204375 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_307270,RMVar_hsa_circ_200058,RMVar_hsa_circ_67892,RMVar_hsa_circ_367484,RMVar_hsa_circ_310655 51373 RMVar_ID_51373 Human_SNP_ID_72967283 A-to-I Human chr2 - 55612824 55612824 55612824 CTCCTGCCTCAGCCTCCCAAGTAGTTGGGACTACAGGCGCCCGCCACCACGCCCAGTTAATTTTT CTCCTGCCTCAGCCTCCCAAGTAGTTGGGACTGCAGGCGCCCGCCACCACGCCCAGTTAATTTTT T C PPP4R3B Ensembl:ENSG00000275052 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1489903881 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_307270,RMVar_hsa_circ_200058,RMVar_hsa_circ_67892,RMVar_hsa_circ_367484,RMVar_hsa_circ_310655 51374 RMVar_ID_51374 Human_SNP_ID_72967369 A-to-I Human chr2 - 55612989 55612989 55612989 CTCCAATTTCAGCCTTCTGAGTAGATGGGATTATGGATGTGAGCCACCATGCTTGACTAATTTTT CTCCAATTTCAGCCTTCTGAGTAGATGGGATTGTGGATGTGAGCCACCATGCTTGACTAATTTTT T C PPP4R3B Ensembl:ENSG00000275052 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1248071139 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_6932413,Human_RBP_ID_13920307 RMVar_hsa_circ_307270,RMVar_hsa_circ_200058,RMVar_hsa_circ_67892,RMVar_hsa_circ_367484,RMVar_hsa_circ_310655 51375 RMVar_ID_51375 Human_SNP_ID_72968117 A-to-I Human chr2 - 55615430 55615430 55615430 CAGAAACAACAGGCAAGTAGTTGTTTATCTTTAATTTGAAAGACTTCATCTGTGATCAAGGAAGT CAGAAACAACAGGCAAGTAGTTGTTTATCTTTCATTTGAAAGACTTCATCTGTGATCAAGGAAGT T G PPP4R3B Ensembl:ENSG00000275052 Protein coding intron GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs758999115 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1920116,Human_RBP_ID_19104722,Human_RBP_ID_24489701 Human_Splice_Rec_248670,Human_Splice_Rec_248696,Human_Splice_Rec_248726,Human_Splice_Rec_248756,Human_Splice_Rec_248762 RMVar_hsa_circ_307270,RMVar_hsa_circ_200058,RMVar_hsa_circ_67892,RMVar_hsa_circ_367484,RMVar_hsa_circ_310655 51376 RMVar_ID_51376 Human_SNP_ID_72969849 A-to-I Human chr2 + 55619827 55619827 55619827 GGGCGTGGTGGTGGGGGCCTGTAATCCCAGCTACTTGGGAGGCCGAGGTAGGAGAATCGCTTCAA GGGCGTGGTGGTGGGGGCCTGTAATCCCAGCTTCTTGGGAGGCCGAGGTAGGAGAATCGCTTCAA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1402615270 Functional Loss SNV dbSNP153 33..33 33 - - - 51377 RMVar_ID_51377 Human_SNP_ID_72971787 A-to-I Human chr2 + 55626952 55626952 55626952 ATTCTGTTTTCTAGACTGGAGTACAGTGGTGCAATCTTGGCTCATTGCAACCTCTACCTCTTGGG ATTCTGTTTTCTAGACTGGAGTACAGTGGTGCGATCTTGGCTCATTGCAACCTCTACCTCTTGGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1267636778 Functional Loss SNV dbSNP153 33..33 33 - - - 51378 RMVar_ID_51378 Human_SNP_ID_72972002 A-to-I Human chr2 + 55627658 55627658 55627658 AAAATTAACCAGGCATGGTAGTCCATACCTGTAGTACCAGCTACTTGGGAGGCTGAGGCAGGAGG AAAATTAACCAGGCATGGTAGTCCATACCTGTGGTACCAGCTACTTGGGAGGCTGAGGCAGGAGG A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1215323152 Functional Loss SNV dbSNP153 33..33 33 - - - 51379 RMVar_ID_51379 Human_SNP_ID_72980043 A-to-I Human chr2 - 55654072 55654072 55654072 TTGTATTTTTAGTCGAGACGGGGTTTCACCATATTGGCCAGGCTGACCTCGAACTCCTGACCTCG TTGTATTTTTAGTCGAGACGGGGTTTCACCATGTTGGCCAGGCTGACCTCGAACTCCTGACCTCG T C PNPT1 Ensembl:ENSG00000138035 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs536593986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25551351 RMVar_hsa_circ_95213,RMVar_hsa_circ_113405,RMVar_hsa_circ_120288,RMVar_hsa_circ_200079,RMVar_hsa_circ_200080,RMVar_hsa_circ_200082,RMVar_hsa_circ_200083,RMVar_hsa_circ_362348,RMVar_hsa_circ_367895,RMVar_hsa_circ_124606,RMVar_hsa_circ_119178,RMVar_hsa_circ_200088,RMVar_hsa_circ_200089,RMVar_hsa_circ_88943,RMVar_hsa_circ_109983,RMVar_hsa_circ_31717,RMVar_hsa_circ_57052,RMVar_hsa_circ_200092,RMVar_hsa_circ_200093,RMVar_hsa_circ_200091,RMVar_hsa_circ_57208,RMVar_hsa_circ_91094,RMVar_hsa_circ_200094,RMVar_hsa_circ_200095,RMVar_hsa_circ_329548,RMVar_hsa_circ_357916,RMVar_hsa_circ_362512,RMVar_hsa_circ_356184,RMVar_hsa_circ_200104,RMVar_hsa_circ_64638,RMVar_hsa_circ_200099,RMVar_hsa_circ_266803,RMVar_hsa_circ_124374,RMVar_hsa_circ_200102,RMVar_hsa_circ_99184,RMVar_hsa_circ_378748,RMVar_hsa_circ_29786,RMVar_hsa_circ_324216,RMVar_hsa_circ_329333,RMVar_hsa_circ_200103,RMVar_hsa_circ_376907,RMVar_hsa_circ_325915,RMVar_hsa_circ_311056,RMVar_hsa_circ_323444,RMVar_hsa_circ_288697,RMVar_hsa_circ_29288 51380 RMVar_ID_51380 Human_SNP_ID_72981470 A-to-I Human chr2 - 55659095 55659095 55659095 TAAAAATTAGCCAAGCATGGTGGCATGTGCCTATAGTCCCAGCTACTCGGGAGGCTGAGATGGGA TAAAAATTAGCCAAGCATGGTGGCATGTGCCTTTAGTCCCAGCTACTCGGGAGGCTGAGATGGGA T A PNPT1 Ensembl:ENSG00000138035 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs552344888 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25551378 RMVar_hsa_circ_1092,RMVar_hsa_circ_95213,RMVar_hsa_circ_113405,RMVar_hsa_circ_120288,RMVar_hsa_circ_200079,RMVar_hsa_circ_200080,RMVar_hsa_circ_200082,RMVar_hsa_circ_200083,RMVar_hsa_circ_362348,RMVar_hsa_circ_367895,RMVar_hsa_circ_119178,RMVar_hsa_circ_200089,RMVar_hsa_circ_88943,RMVar_hsa_circ_109983,RMVar_hsa_circ_31717,RMVar_hsa_circ_200092,RMVar_hsa_circ_200093,RMVar_hsa_circ_200091,RMVar_hsa_circ_57208,RMVar_hsa_circ_91094,RMVar_hsa_circ_200094,RMVar_hsa_circ_329548,RMVar_hsa_circ_357916,RMVar_hsa_circ_362512,RMVar_hsa_circ_200104,RMVar_hsa_circ_64638,RMVar_hsa_circ_200099,RMVar_hsa_circ_266803,RMVar_hsa_circ_124374,RMVar_hsa_circ_200102,RMVar_hsa_circ_99184,RMVar_hsa_circ_378748,RMVar_hsa_circ_324216,RMVar_hsa_circ_329333,RMVar_hsa_circ_200103,RMVar_hsa_circ_325915,RMVar_hsa_circ_311056,RMVar_hsa_circ_323444,RMVar_hsa_circ_288697,RMVar_hsa_circ_39697,RMVar_hsa_circ_325721,RMVar_hsa_circ_29288,RMVar_hsa_circ_377349,RMVar_hsa_circ_341692,RMVar_hsa_circ_64870,RMVar_hsa_circ_6794,RMVar_hsa_circ_36565,RMVar_hsa_circ_299128,RMVar_hsa_circ_355086,RMVar_hsa_circ_14021 51381 RMVar_ID_51381 Human_SNP_ID_72981471 A-to-I Human chr2 - 55659095 55659095 55659095 TAAAAATTAGCCAAGCATGGTGGCATGTGCCTATAGTCCCAGCTACTCGGGAGGCTGAGATGGGA TAAAAATTAGCCAAGCATGGTGGCATGTGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGATGGGA T C PNPT1 Ensembl:ENSG00000138035 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs552344888 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25551378 RMVar_hsa_circ_1092,RMVar_hsa_circ_95213,RMVar_hsa_circ_113405,RMVar_hsa_circ_120288,RMVar_hsa_circ_200079,RMVar_hsa_circ_200080,RMVar_hsa_circ_200082,RMVar_hsa_circ_200083,RMVar_hsa_circ_362348,RMVar_hsa_circ_367895,RMVar_hsa_circ_119178,RMVar_hsa_circ_200089,RMVar_hsa_circ_88943,RMVar_hsa_circ_109983,RMVar_hsa_circ_31717,RMVar_hsa_circ_200092,RMVar_hsa_circ_200093,RMVar_hsa_circ_200091,RMVar_hsa_circ_57208,RMVar_hsa_circ_91094,RMVar_hsa_circ_200094,RMVar_hsa_circ_329548,RMVar_hsa_circ_357916,RMVar_hsa_circ_362512,RMVar_hsa_circ_200104,RMVar_hsa_circ_64638,RMVar_hsa_circ_200099,RMVar_hsa_circ_266803,RMVar_hsa_circ_124374,RMVar_hsa_circ_200102,RMVar_hsa_circ_99184,RMVar_hsa_circ_378748,RMVar_hsa_circ_324216,RMVar_hsa_circ_329333,RMVar_hsa_circ_200103,RMVar_hsa_circ_325915,RMVar_hsa_circ_311056,RMVar_hsa_circ_323444,RMVar_hsa_circ_288697,RMVar_hsa_circ_39697,RMVar_hsa_circ_325721,RMVar_hsa_circ_29288,RMVar_hsa_circ_377349,RMVar_hsa_circ_341692,RMVar_hsa_circ_64870,RMVar_hsa_circ_6794,RMVar_hsa_circ_36565,RMVar_hsa_circ_299128,RMVar_hsa_circ_355086,RMVar_hsa_circ_14021 51382 RMVar_ID_51382 Human_SNP_ID_72982435 A-to-I Human chr2 - 55662588 55662588 55662588 CTCACTGCAACCTCGCCTGTTGGATTCGAGCTATTCTTCTGCCTCAGCCTCCCAAGCAGCTGGGA CTCACTGCAACCTCGCCTGTTGGATTCGAGCTGTTCTTCTGCCTCAGCCTCCCAAGCAGCTGGGA T C PNPT1 Ensembl:ENSG00000138035 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs577448925 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25551409 RMVar_hsa_circ_1092,RMVar_hsa_circ_95213,RMVar_hsa_circ_113405,RMVar_hsa_circ_120288,RMVar_hsa_circ_200079,RMVar_hsa_circ_200080,RMVar_hsa_circ_200083,RMVar_hsa_circ_362348,RMVar_hsa_circ_367895,RMVar_hsa_circ_119178,RMVar_hsa_circ_200089,RMVar_hsa_circ_109983,RMVar_hsa_circ_31717,RMVar_hsa_circ_200092,RMVar_hsa_circ_200093,RMVar_hsa_circ_57208,RMVar_hsa_circ_91094,RMVar_hsa_circ_200094,RMVar_hsa_circ_329548,RMVar_hsa_circ_357916,RMVar_hsa_circ_200104,RMVar_hsa_circ_64638,RMVar_hsa_circ_200099,RMVar_hsa_circ_266803,RMVar_hsa_circ_124374,RMVar_hsa_circ_200102,RMVar_hsa_circ_99184,RMVar_hsa_circ_324216,RMVar_hsa_circ_329333,RMVar_hsa_circ_311056,RMVar_hsa_circ_323444,RMVar_hsa_circ_288697,RMVar_hsa_circ_39697,RMVar_hsa_circ_29288,RMVar_hsa_circ_377349,RMVar_hsa_circ_341692,RMVar_hsa_circ_64870,RMVar_hsa_circ_6794,RMVar_hsa_circ_36565,RMVar_hsa_circ_355086,RMVar_hsa_circ_14021,RMVar_hsa_circ_9112,RMVar_hsa_circ_200105,RMVar_hsa_circ_37316,RMVar_hsa_circ_50100,RMVar_hsa_circ_344819,RMVar_hsa_circ_371182,RMVar_hsa_circ_301581,RMVar_hsa_circ_47920,RMVar_hsa_circ_308967,RMVar_hsa_circ_341419,RMVar_hsa_circ_355724,RMVar_hsa_circ_364807,RMVar_hsa_circ_314778,RMVar_hsa_circ_300426,RMVar_hsa_circ_200106,RMVar_hsa_circ_200107,RMVar_hsa_circ_200108 51383 RMVar_ID_51383 Human_SNP_ID_72982571 A-to-I Human chr2 - 55663029 55663029 55663029 ATACAAAAAATTAGCTGGGCGTGGTGGCACGCACCTGTAGTCCCAGCTACTTACTCAGGAGGCTG ATACAAAAAATTAGCTGGGCGTGGTGGCACGCCCCTGTAGTCCCAGCTACTTACTCAGGAGGCTG T G PNPT1 Ensembl:ENSG00000138035 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1247673450 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1092,RMVar_hsa_circ_95213,RMVar_hsa_circ_113405,RMVar_hsa_circ_120288,RMVar_hsa_circ_200079,RMVar_hsa_circ_200080,RMVar_hsa_circ_200083,RMVar_hsa_circ_362348,RMVar_hsa_circ_367895,RMVar_hsa_circ_119178,RMVar_hsa_circ_200089,RMVar_hsa_circ_109983,RMVar_hsa_circ_31717,RMVar_hsa_circ_200092,RMVar_hsa_circ_200093,RMVar_hsa_circ_57208,RMVar_hsa_circ_91094,RMVar_hsa_circ_200094,RMVar_hsa_circ_329548,RMVar_hsa_circ_357916,RMVar_hsa_circ_200104,RMVar_hsa_circ_64638,RMVar_hsa_circ_200099,RMVar_hsa_circ_266803,RMVar_hsa_circ_124374,RMVar_hsa_circ_200102,RMVar_hsa_circ_99184,RMVar_hsa_circ_324216,RMVar_hsa_circ_329333,RMVar_hsa_circ_311056,RMVar_hsa_circ_323444,RMVar_hsa_circ_288697,RMVar_hsa_circ_39697,RMVar_hsa_circ_29288,RMVar_hsa_circ_377349,RMVar_hsa_circ_341692,RMVar_hsa_circ_64870,RMVar_hsa_circ_6794,RMVar_hsa_circ_36565,RMVar_hsa_circ_355086,RMVar_hsa_circ_14021,RMVar_hsa_circ_9112,RMVar_hsa_circ_200105,RMVar_hsa_circ_37316,RMVar_hsa_circ_50100,RMVar_hsa_circ_344819,RMVar_hsa_circ_371182,RMVar_hsa_circ_301581,RMVar_hsa_circ_47920,RMVar_hsa_circ_308967,RMVar_hsa_circ_341419,RMVar_hsa_circ_355724,RMVar_hsa_circ_364807,RMVar_hsa_circ_314778,RMVar_hsa_circ_300426,RMVar_hsa_circ_200106,RMVar_hsa_circ_200107,RMVar_hsa_circ_200108 51384 RMVar_ID_51384 Human_SNP_ID_72983414 A-to-I Human chr2 - 55666332 55666332 55666332 ATTGCTTGAGGCCAGGAGTTCGAGGTTGCAATAATCTATGGTCATGCCATTGCACTCCAGCCTGG ATTGCTTGAGGCCAGGAGTTCGAGGTTGCAATGATCTATGGTCATGCCATTGCACTCCAGCCTGG T C PNPT1 Ensembl:ENSG00000138035 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1205111054 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25589944 RMVar_hsa_circ_1092,RMVar_hsa_circ_95213,RMVar_hsa_circ_113405,RMVar_hsa_circ_120288,RMVar_hsa_circ_200079,RMVar_hsa_circ_200080,RMVar_hsa_circ_200083,RMVar_hsa_circ_362348,RMVar_hsa_circ_367895,RMVar_hsa_circ_119178,RMVar_hsa_circ_200089,RMVar_hsa_circ_109983,RMVar_hsa_circ_31717,RMVar_hsa_circ_200092,RMVar_hsa_circ_200093,RMVar_hsa_circ_57208,RMVar_hsa_circ_91094,RMVar_hsa_circ_200094,RMVar_hsa_circ_329548,RMVar_hsa_circ_357916,RMVar_hsa_circ_200104,RMVar_hsa_circ_64638,RMVar_hsa_circ_200099,RMVar_hsa_circ_266803,RMVar_hsa_circ_124374,RMVar_hsa_circ_200102,RMVar_hsa_circ_99184,RMVar_hsa_circ_324216,RMVar_hsa_circ_329333,RMVar_hsa_circ_311056,RMVar_hsa_circ_323444,RMVar_hsa_circ_288697,RMVar_hsa_circ_39697,RMVar_hsa_circ_29288,RMVar_hsa_circ_377349,RMVar_hsa_circ_341692,RMVar_hsa_circ_64870,RMVar_hsa_circ_6794,RMVar_hsa_circ_36565,RMVar_hsa_circ_355086,RMVar_hsa_circ_14021,RMVar_hsa_circ_9112,RMVar_hsa_circ_200105,RMVar_hsa_circ_37316,RMVar_hsa_circ_50100,RMVar_hsa_circ_344819,RMVar_hsa_circ_371182,RMVar_hsa_circ_301581,RMVar_hsa_circ_47920,RMVar_hsa_circ_308967,RMVar_hsa_circ_341419,RMVar_hsa_circ_355724,RMVar_hsa_circ_364807,RMVar_hsa_circ_314778,RMVar_hsa_circ_300426,RMVar_hsa_circ_200106,RMVar_hsa_circ_200107,RMVar_hsa_circ_200108 51385 RMVar_ID_51385 Human_SNP_ID_72985739 A-to-I Human chr2 - 55674182 55674182 55674182 TTAGCTATTTCTAATGCAATAGAAAAAATTCTATTATTCAGTCCTTTAGTTGGCTTACTTGAAAC TTAGCTATTTCTAATGCAATAGAAAAAATTCTGTTATTCAGTCCTTTAGTTGGCTTACTTGAAAC T C PNPT1 Ensembl:ENSG00000138035 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs12617829 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_6604,GWAS_ID_6605,GWAS_ID_6606,GWAS_ID_6607,GWAS_ID_6608,GWAS_ID_6609 RMVar_hsa_circ_1092,RMVar_hsa_circ_95213,RMVar_hsa_circ_113405,RMVar_hsa_circ_120288,RMVar_hsa_circ_200079,RMVar_hsa_circ_200080,RMVar_hsa_circ_200083,RMVar_hsa_circ_367895,RMVar_hsa_circ_119178,RMVar_hsa_circ_200089,RMVar_hsa_circ_109983,RMVar_hsa_circ_31717,RMVar_hsa_circ_200092,RMVar_hsa_circ_200093,RMVar_hsa_circ_57208,RMVar_hsa_circ_91094,RMVar_hsa_circ_200094,RMVar_hsa_circ_357916,RMVar_hsa_circ_200104,RMVar_hsa_circ_64638,RMVar_hsa_circ_200099,RMVar_hsa_circ_266803,RMVar_hsa_circ_124374,RMVar_hsa_circ_200102,RMVar_hsa_circ_99184,RMVar_hsa_circ_324216,RMVar_hsa_circ_329333,RMVar_hsa_circ_29288,RMVar_hsa_circ_377349,RMVar_hsa_circ_341692,RMVar_hsa_circ_64870,RMVar_hsa_circ_14021,RMVar_hsa_circ_9112,RMVar_hsa_circ_50100,RMVar_hsa_circ_47920,RMVar_hsa_circ_364807,RMVar_hsa_circ_314778,RMVar_hsa_circ_300426,RMVar_hsa_circ_200106,RMVar_hsa_circ_200107,RMVar_hsa_circ_334922,RMVar_hsa_circ_314053,RMVar_hsa_circ_325657,RMVar_hsa_circ_343703,RMVar_hsa_circ_200110,RMVar_hsa_circ_71823 51386 RMVar_ID_51386 Human_SNP_ID_72985795 A-to-I Human chr2 - 55674410 55674410 55674410 TCTTTCATTTTTTATAGAGACAGGACCTCGCTATGTTGCCCAGGCTGGTCTTGAACTCTGACTTC TCTTTCATTTTTTATAGAGACAGGACCTCGCTGTGTTGCCCAGGCTGGTCTTGAACTCTGACTTC T C PNPT1 Ensembl:ENSG00000138035 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs949973790 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_13921107,Human_RBP_ID_25551512 RMVar_hsa_circ_1092,RMVar_hsa_circ_95213,RMVar_hsa_circ_113405,RMVar_hsa_circ_120288,RMVar_hsa_circ_200079,RMVar_hsa_circ_200080,RMVar_hsa_circ_200083,RMVar_hsa_circ_367895,RMVar_hsa_circ_119178,RMVar_hsa_circ_200089,RMVar_hsa_circ_109983,RMVar_hsa_circ_31717,RMVar_hsa_circ_200092,RMVar_hsa_circ_200093,RMVar_hsa_circ_57208,RMVar_hsa_circ_91094,RMVar_hsa_circ_200094,RMVar_hsa_circ_357916,RMVar_hsa_circ_200104,RMVar_hsa_circ_64638,RMVar_hsa_circ_200099,RMVar_hsa_circ_266803,RMVar_hsa_circ_124374,RMVar_hsa_circ_200102,RMVar_hsa_circ_99184,RMVar_hsa_circ_324216,RMVar_hsa_circ_329333,RMVar_hsa_circ_29288,RMVar_hsa_circ_377349,RMVar_hsa_circ_341692,RMVar_hsa_circ_64870,RMVar_hsa_circ_14021,RMVar_hsa_circ_9112,RMVar_hsa_circ_50100,RMVar_hsa_circ_47920,RMVar_hsa_circ_364807,RMVar_hsa_circ_314778,RMVar_hsa_circ_300426,RMVar_hsa_circ_200106,RMVar_hsa_circ_200107,RMVar_hsa_circ_334922,RMVar_hsa_circ_314053,RMVar_hsa_circ_325657,RMVar_hsa_circ_343703,RMVar_hsa_circ_200110,RMVar_hsa_circ_71823 51387 RMVar_ID_51387 Human_SNP_ID_73679405 A-to-I Human chr2 + 58110382 58110382 58110382 ATAACATACCATAATGCAAAAATCTTAACAATAAATCAAATGCATATTTACGAAAATAACTATAT ATAACATACCATAATGCAAAAATCTTAACAATGAATCAAATGCATATTTACGAAAATAACTATAT A G VRK2 Ensembl:ENSG00000028116 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs533779716 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_353433,RMVar_hsa_circ_356263,RMVar_hsa_circ_367385,RMVar_hsa_circ_74688,RMVar_hsa_circ_335765,RMVar_hsa_circ_344715,RMVar_hsa_circ_346531,RMVar_hsa_circ_304221,RMVar_hsa_circ_46799 51388 RMVar_ID_51388 Human_SNP_ID_73710785 A-to-I Human chr2 - 58214808 58214808 58214808 CATAAGGCAAGACTTAAGATTCCTCATGGGCCAGGTGTGGTGGCTCACACCTGTAATCCCAGTAC CATAAGGCAAGACTTAAGATTCCTCATGGGCCGGGTGTGGTGGCTCACACCTGTAATCCCAGTAC T C FANCL Ensembl:ENSG00000115392 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1162115561 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_200149,RMVar_hsa_circ_8307,RMVar_hsa_circ_200139,RMVar_hsa_circ_53134,RMVar_hsa_circ_64191,RMVar_hsa_circ_318820,RMVar_hsa_circ_376295,RMVar_hsa_circ_20963,RMVar_hsa_circ_200142,RMVar_hsa_circ_200145,RMVar_hsa_circ_335041,RMVar_hsa_circ_369957,RMVar_hsa_circ_200147,RMVar_hsa_circ_288621,RMVar_hsa_circ_200146,RMVar_hsa_circ_271999,RMVar_hsa_circ_289740,RMVar_hsa_circ_272910,RMVar_hsa_circ_200150,RMVar_hsa_circ_200151,RMVar_hsa_circ_374870 51389 RMVar_ID_51389 Human_SNP_ID_73714993 A-to-I Human chr2 + 58228010 58228008 58228010 AGGAGTATAAAATATAAAAATCAGGCAACTCTATGTAATTTTTAAAATCTAGTGGCAGCAATAAA AGGAGTATAAAATATAAAAATCAGGCAACTC__TGTAATTTTTAAAATCTAGTGGCAGCAATAAA CTA C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1462389121 Functional Loss DEL dbSNP153 32..33 33 - - - 51390 RMVar_ID_51390 Human_SNP_ID_73714994 A-to-I Human chr2 + 58228010 58228010 58228010 AGGAGTATAAAATATAAAAATCAGGCAACTCTATGTAATTTTTAAAATCTAGTGGCAGCAATAAA AGGAGTATAAAATATAAAAATCAGGCAACTCTGTGTAATTTTTAAAATCTAGTGGCAGCAATAAA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs557305496 Functional Loss SNV dbSNP153 33..33 33 - - - 51391 RMVar_ID_51391 Human_SNP_ID_73721570 A-to-I Human chr2 + 58251976 58251976 58251976 CCAAATGAGCTCATCCTGGGCTGGTACGCTACAGGCCATGACATCACAGAGCACTCTGTGCTGAT CCAAATGAGCTCATCCTGGGCTGGTACGCTACCGGCCATGACATCACAGAGCACTCTGTGCTGAT A C EIF3FP3 Ensembl:ENSG00000233426 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-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 51392 RMVar_ID_51392 Human_SNP_ID_73721571 A-to-I Human chr2 + 58251976 58251976 58251976 CCAAATGAGCTCATCCTGGGCTGGTACGCTACAGGCCATGACATCACAGAGCACTCTGTGCTGAT CCAAATGAGCTCATCCTGGGCTGGTACGCTACGGGCCATGACATCACAGAGCACTCTGTGCTGAT A G EIF3FP3 Ensembl:ENSG00000233426 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-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 51393 RMVar_ID_51393 Human_SNP_ID_73721616 A-to-I Human chr2 - 58252099 58252099 58252099 GTCCTCCCAGGGACACCCATTAAAGTGCTGACATAGGCTTTGATGCTCATGCGGCCGTTCTGGAG GTCCTCCCAGGGACACCCATTAAAGTGCTGACGTAGGCTTTGATGCTCATGCGGCCGTTCTGGAG T C lnc-FANCL-4 RNACentral:URS00008B7619 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878880258 Functional Loss SNV dbSNP153 33..33 33 - - - 51394 RMVar_ID_51394 Human_SNP_ID_73778339 A-to-I Human chr2 - 58460523 58460523 58460523 AAATGGACCAGGGTAACAAGAAGAGAACCTTAAGCCGTTGGGACTTTGATACCCAGGAAGACTAC AAATGGACCAGGGTAACAAGAAGAGAACCTTAGGCCGTTGGGACTTTGATACCCAGGAAGACTAC T C AC007238.1 Ensembl:ENSG00000231043 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879041651 Functional Loss SNV dbSNP153 33..33 33 - - - 51395 RMVar_ID_51395 Human_SNP_ID_73778343 A-to-I Human chr2 - 58460530 58460530 58460530 TATAGCAAAATGGACCAGGGTAACAAGAAGAGAACCTTAAGCCGTTGGGACTTTGATACCCAGGA TATAGCAAAATGGACCAGGGTAACAAGAAGAGGACCTTAAGCCGTTGGGACTTTGATACCCAGGA T C AC007238.1 Ensembl:ENSG00000231043 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878937359 Functional Loss SNV dbSNP153 33..33 33 - - - 51396 RMVar_ID_51396 Human_SNP_ID_73778344 A-to-I Human chr2 - 58460532 58460532 58460532 ATTATAGCAAAATGGACCAGGGTAACAAGAAGAGAACCTTAAGCCGTTGGGACTTTGATACCCAG ATTATAGCAAAATGGACCAGGGTAACAAGAAGGGAACCTTAAGCCGTTGGGACTTTGATACCCAG T C AC007238.1 Ensembl:ENSG00000231043 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879060754 Functional Loss SNV dbSNP153 33..33 33 - - - 51397 RMVar_ID_51397 Human_SNP_ID_73778590 A-to-I Human chr2 + 58461162 58461157 58461163 GAAAGCAACTGGGTAAGCTTGCTAATGACAATATCATTTGTGGTCAGTATGGTCTGGGCCTCCAT GAAAGCAACTGGGTAAGCTTGCTAATGA______CATTTGTGGTCAGTATGGTCTGGGCCTCCAT ACAATAT A LINC01122 Ensembl:ENSG00000233723 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs780866248 Functional Loss DEL dbSNP153 29..34 33 - - - 51398 RMVar_ID_51398 Human_SNP_ID_73778592 A-to-I Human chr2 + 58461162 58461162 58461162 GAAAGCAACTGGGTAAGCTTGCTAATGACAATATCATTTGTGGTCAGTATGGTCTGGGCCTCCAT GAAAGCAACTGGGTAAGCTTGCTAATGACAATGTCATTTGTGGTCAGTATGGTCTGGGCCTCCAT A G LINC01122 Ensembl:ENSG00000233723 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1197069272 Functional Loss SNV dbSNP153 33..33 33 - - - 51399 RMVar_ID_51399 Human_SNP_ID_73778596 A-to-I Human chr2 + 58461178 58461178 58461178 GCTTGCTAATGACAATATCATTTGTGGTCAGTATGGTCTGGGCCTCCATGGTGGGGCAGTCAACC GCTTGCTAATGACAATATCATTTGTGGTCAGTGTGGTCTGGGCCTCCATGGTGGGGCAGTCAACC A G LINC01122 Ensembl:ENSG00000233723 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1268047432 Functional Loss SNV dbSNP153 33..33 33 - - - 51400 RMVar_ID_51400 Human_SNP_ID_73778602 A-to-I Human chr2 + 58461207 58461207 58461207 AGTATGGTCTGGGCCTCCATGGTGGGGCAGTCAACCTTGCTGCGGATAAGAGTGGTGGGGATATC AGTATGGTCTGGGCCTCCATGGTGGGGCAGTCGACCTTGCTGCGGATAAGAGTGGTGGGGATATC A G LINC01122 Ensembl:ENSG00000233723 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs988767252 Functional Loss SNV dbSNP153 33..33 33 - - - 51401 RMVar_ID_51401 Human_SNP_ID_73778704 A-to-I Human chr2 - 58461589 58461589 58461589 CAGCTAACTACAGGGCTGTTGGCCCCACTACTAAGGCGGACAAATCAGCTGCAGAGAAGAGAAGA CAGCTAACTACAGGGCTGTTGGCCCCACTACTGAGGCGGACAAATCAGCTGCAGAGAAGAGAAGA T C AC007238.1 Ensembl:ENSG00000231043 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878879180 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_1823556 51402 RMVar_ID_51402 Human_SNP_ID_73778705 A-to-I Human chr2 - 58461592 58461592 58461592 CCACAGCTAACTACAGGGCTGTTGGCCCCACTACTAAGGCGGACAAATCAGCTGCAGAGAAGAGA CCACAGCTAACTACAGGGCTGTTGGCCCCACTGCTAAGGCGGACAAATCAGCTGCAGAGAAGAGA T C AC007238.1 Ensembl:ENSG00000231043 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879198444 Functional Loss SNV dbSNP153 33..33 33 - - - 51403 RMVar_ID_51403 Human_SNP_ID_252835845 A-to-I Human chr5 + 136857899 136857898 136857900 GGCTGCTGAAAAAAATCGGCTTACTACAGTACAGAGACTACTTTCTGAAAAGGCTGCTCATGTGA GGCTGCTGAAAAAAATCGGCTTACTACAGTAC__AGACTACTTTCTGAAAAGGCTGCTCATGTGA CAG C ANKRD49P3 Ensembl:ENSG00000248616 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1386639415 Functional Loss DEL dbSNP153 33..34 33 - - - 51404 RMVar_ID_51404 Human_SNP_ID_252835846 A-to-I Human chr5 + 136857899 136857899 136857899 GGCTGCTGAAAAAAATCGGCTTACTACAGTACAGAGACTACTTTCTGAAAAGGCTGCTCATGTGA GGCTGCTGAAAAAAATCGGCTTACTACAGTACTGAGACTACTTTCTGAAAAGGCTGCTCATGTGA A T ANKRD49P3 Ensembl:ENSG00000248616 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167205720 Functional Loss SNV dbSNP153 33..33 33 - - - 51405 RMVar_ID_51405 Human_SNP_ID_252835847 A-to-I Human chr5 + 136857906 136857906 136857906 GAAAAAAATCGGCTTACTACAGTACAGAGACTACTTTCTGAAAAGGCTGCTCATGTGAACACTAG GAAAAAAATCGGCTTACTACAGTACAGAGACTGCTTTCTGAAAAGGCTGCTCATGTGAACACTAG A G ANKRD49P3 Ensembl:ENSG00000248616 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs749947574 Functional Loss SNV dbSNP153 33..33 33 - - - 51406 RMVar_ID_51406 Human_SNP_ID_252940362 A-to-I Human chr5 - 137304026 137304026 137304026 CATTTTGGGGAAAAAGTCATCTAAAAGTAGATAGATTTTCAGTGTGAAGTGAAGGATGCCTACGT CATTTTGGGGAAAAAGTCATCTAAAAGTAGATGGATTTTCAGTGTGAAGTGAAGGATGCCTACGT T C SPOCK1 Ensembl:ENSG00000152377 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1237782166 Functional Loss SNV dbSNP153 33..33 33 - - - 51407 RMVar_ID_51407 Human_SNP_ID_252970747 A-to-I Human chr5 - 137435962 137435962 137435962 TTTAGTAGAGACTGGGTTTTGCCACGTTGCCCAGGCTGGTCTTGAACTCCTGACCTCAGGTGGTC TTTAGTAGAGACTGGGTTTTGCCACGTTGCCCGGGCTGGTCTTGAACTCCTGACCTCAGGTGGTC T C SPOCK1 Ensembl:ENSG00000152377 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1287326307 Functional Loss SNV dbSNP153 33..33 33 - - - 51408 RMVar_ID_51408 Human_SNP_ID_252979839 A-to-I Human chr5 - 137476825 137476825 137476825 CACCTCCCAGGTTCAAGCGATCCTTCCACCTCAGCCTTCCAAGTAGCTGGGATTACAGACACCTG CACCTCCCAGGTTCAAGCGATCCTTCCACCTCTGCCTTCCAAGTAGCTGGGATTACAGACACCTG T A SPOCK1 Ensembl:ENSG00000152377 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1561545837 Functional Loss SNV dbSNP153 33..33 33 - - - 51409 RMVar_ID_51409 Human_SNP_ID_253021952 A-to-I Human chr5 - 137652774 137652774 137652774 TCCATTCTCTTAACTATTTTCAAGAATATAATACATTGTTATTAACTATAGTCACCACGTTGTAC TCCATTCTCTTAACTATTTTCAAGAATATAATGCATTGTTATTAACTATAGTCACCACGTTGTAC T C KLHL3 Ensembl:ENSG00000146021 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs968798949 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_21661,RMVar_hsa_circ_234682,RMVar_hsa_circ_70473,RMVar_hsa_circ_109540,RMVar_hsa_circ_234685,RMVar_hsa_circ_69125 51410 RMVar_ID_51410 Human_SNP_ID_253070450 A-to-I Human chr5 - 137878465 137878465 137878465 CAAGTTGAGGCCAGGCGTGGTGGCTCATGCCTATAATCCTAGCACTTTTGGAGGCCGAGGCGTTC CAAGTTGAGGCCAGGCGTGGTGGCTCATGCCTGTAATCCTAGCACTTTTGGAGGCCGAGGCGTTC T C AC106791.1 Ensembl:ENSG00000250159 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs767357137 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25858359 51411 RMVar_ID_51411 Human_SNP_ID_253070451 A-to-I Human chr5 - 137878465 137878465 137878465 CAAGTTGAGGCCAGGCGTGGTGGCTCATGCCTATAATCCTAGCACTTTTGGAGGCCGAGGCGTTC CAAGTTGAGGCCAGGCGTGGTGGCTCATGCCTCTAATCCTAGCACTTTTGGAGGCCGAGGCGTTC T G AC106791.1 Ensembl:ENSG00000250159 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs767357137 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25858359 51412 RMVar_ID_51412 Human_SNP_ID_253070599 A-to-I Human chr5 - 137879076 137879076 137879076 TACAAAAACTAGCCAGCACGGTGTGCGCACCTATAGTCCCATCTATTTGGGAGTCTGAGGCACGA TACAAAAACTAGCCAGCACGGTGTGCGCACCTGTAGTCCCATCTATTTGGGAGTCTGAGGCACGA T C AC106791.1 Ensembl:ENSG00000250159 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1384309398 Functional Loss SNV dbSNP153 33..33 33 - - - 51413 RMVar_ID_51413 Human_SNP_ID_253071302 A-to-I Human chr5 - 137881835 137881835 137881835 TCTTGTTGCCCAGGCTGGAGTACAGTGGCCCAATCTCAGCTCACTCAGGAGGCTAAGGCAGGAGA TCTTGTTGCCCAGGCTGGAGTACAGTGGCCCAGTCTCAGCTCACTCAGGAGGCTAAGGCAGGAGA T C AC106791.1 Ensembl:ENSG00000250159 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs554138266 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5250677 51414 RMVar_ID_51414 Human_SNP_ID_253091030 A-to-I Human chr5 - 137964384 137964384 137964384 GGTCTGGTTGTGCACAGTGGCTCATGCCTGTAATCCCAGGACTTTGGGAGGCTGAAGACAGATGG GGTCTGGTTGTGCACAGTGGCTCATGCCTGTAGTCCCAGGACTTTGGGAGGCTGAAGACAGATGG T C FAM13B Ensembl:ENSG00000031003 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs772436395 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16545,RMVar_hsa_circ_2085,RMVar_hsa_circ_112333,RMVar_hsa_circ_30640,RMVar_hsa_circ_234704,RMVar_hsa_circ_234711,RMVar_hsa_circ_25179,RMVar_hsa_circ_101914,RMVar_hsa_circ_234712,RMVar_hsa_circ_351149,RMVar_hsa_circ_312134,RMVar_hsa_circ_22020,RMVar_hsa_circ_15172,RMVar_hsa_circ_234714,RMVar_hsa_circ_234715,RMVar_hsa_circ_370360,RMVar_hsa_circ_31307,RMVar_hsa_circ_285318,RMVar_hsa_circ_234719,RMVar_hsa_circ_308204,RMVar_hsa_circ_298525,RMVar_hsa_circ_94237,RMVar_hsa_circ_87011,RMVar_hsa_circ_234721,RMVar_hsa_circ_234722,RMVar_hsa_circ_234720,RMVar_hsa_circ_18365,RMVar_hsa_circ_76620,RMVar_hsa_circ_234725,RMVar_hsa_circ_234726,RMVar_hsa_circ_118587,RMVar_hsa_circ_4060,RMVar_hsa_circ_57346,RMVar_hsa_circ_234727,RMVar_hsa_circ_312126,RMVar_hsa_circ_350683,RMVar_hsa_circ_234729,RMVar_hsa_circ_108735,RMVar_hsa_circ_44785,RMVar_hsa_circ_234730 51415 RMVar_ID_51415 Human_SNP_ID_253095259 A-to-I Human chr5 - 137979169 137979169 137979169 ATCTCTACTAAAAATACAAAAATTAGCGGGGCATGATGGCACATGCTTGTAATCCCAGCTACTCG ATCTCTACTAAAAATACAAAAATTAGCGGGGCGTGATGGCACATGCTTGTAATCCCAGCTACTCG T C FAM13B Ensembl:ENSG00000031003 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs981709343 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16545,RMVar_hsa_circ_2085,RMVar_hsa_circ_112333,RMVar_hsa_circ_30640,RMVar_hsa_circ_234704,RMVar_hsa_circ_234711,RMVar_hsa_circ_25179,RMVar_hsa_circ_101914,RMVar_hsa_circ_234712,RMVar_hsa_circ_351149,RMVar_hsa_circ_312134,RMVar_hsa_circ_22020,RMVar_hsa_circ_15172,RMVar_hsa_circ_234714,RMVar_hsa_circ_234715,RMVar_hsa_circ_370360,RMVar_hsa_circ_31307,RMVar_hsa_circ_285318,RMVar_hsa_circ_234719,RMVar_hsa_circ_308204,RMVar_hsa_circ_298525,RMVar_hsa_circ_94237,RMVar_hsa_circ_87011,RMVar_hsa_circ_234721,RMVar_hsa_circ_234722,RMVar_hsa_circ_234720,RMVar_hsa_circ_18365,RMVar_hsa_circ_76620,RMVar_hsa_circ_234725,RMVar_hsa_circ_234726,RMVar_hsa_circ_118587,RMVar_hsa_circ_4060,RMVar_hsa_circ_57346,RMVar_hsa_circ_234727,RMVar_hsa_circ_312126,RMVar_hsa_circ_350683,RMVar_hsa_circ_234729,RMVar_hsa_circ_108735,RMVar_hsa_circ_44785,RMVar_hsa_circ_234730 51416 RMVar_ID_51416 Human_SNP_ID_253095446 A-to-I Human chr5 - 137979905 137979905 137979905 CTCGCGCCTTGGCCTCCCAAAGTGCTGGGATTATAGGCGTGAGCCACCGTGCCTGGTCGATTTAA CTCGCGCCTTGGCCTCCCAAAGTGCTGGGATTGTAGGCGTGAGCCACCGTGCCTGGTCGATTTAA T C FAM13B Ensembl:ENSG00000031003 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs987223019 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_16545,RMVar_hsa_circ_2085,RMVar_hsa_circ_112333,RMVar_hsa_circ_30640,RMVar_hsa_circ_234704,RMVar_hsa_circ_234711,RMVar_hsa_circ_25179,RMVar_hsa_circ_101914,RMVar_hsa_circ_234712,RMVar_hsa_circ_351149,RMVar_hsa_circ_312134,RMVar_hsa_circ_22020,RMVar_hsa_circ_15172,RMVar_hsa_circ_234714,RMVar_hsa_circ_234715,RMVar_hsa_circ_370360,RMVar_hsa_circ_31307,RMVar_hsa_circ_285318,RMVar_hsa_circ_234719,RMVar_hsa_circ_308204,RMVar_hsa_circ_298525,RMVar_hsa_circ_94237,RMVar_hsa_circ_87011,RMVar_hsa_circ_234721,RMVar_hsa_circ_234722,RMVar_hsa_circ_234720,RMVar_hsa_circ_18365,RMVar_hsa_circ_76620,RMVar_hsa_circ_234725,RMVar_hsa_circ_234726,RMVar_hsa_circ_118587,RMVar_hsa_circ_4060,RMVar_hsa_circ_57346,RMVar_hsa_circ_234727,RMVar_hsa_circ_312126,RMVar_hsa_circ_350683,RMVar_hsa_circ_234729,RMVar_hsa_circ_108735,RMVar_hsa_circ_44785,RMVar_hsa_circ_234730 51417 RMVar_ID_51417 Human_SNP_ID_253095470 A-to-I Human chr5 - 137979977 137979977 137979977 TTTTTTTTTTAGTAGAGACAGGATTTCTCCTTATTGATCAGGCTAGTCTCAAACTCCTGACCTCA TTTTTTTTTTAGTAGAGACAGGATTTCTCCTTTTTGATCAGGCTAGTCTCAAACTCCTGACCTCA T A FAM13B Ensembl:ENSG00000031003 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1265300620 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2897772,Human_RBP_ID_7388385 RMVar_hsa_circ_16545,RMVar_hsa_circ_2085,RMVar_hsa_circ_112333,RMVar_hsa_circ_30640,RMVar_hsa_circ_234704,RMVar_hsa_circ_234711,RMVar_hsa_circ_25179,RMVar_hsa_circ_101914,RMVar_hsa_circ_234712,RMVar_hsa_circ_351149,RMVar_hsa_circ_312134,RMVar_hsa_circ_22020,RMVar_hsa_circ_15172,RMVar_hsa_circ_234714,RMVar_hsa_circ_234715,RMVar_hsa_circ_370360,RMVar_hsa_circ_31307,RMVar_hsa_circ_285318,RMVar_hsa_circ_234719,RMVar_hsa_circ_308204,RMVar_hsa_circ_298525,RMVar_hsa_circ_94237,RMVar_hsa_circ_87011,RMVar_hsa_circ_234721,RMVar_hsa_circ_234722,RMVar_hsa_circ_234720,RMVar_hsa_circ_18365,RMVar_hsa_circ_76620,RMVar_hsa_circ_234725,RMVar_hsa_circ_234726,RMVar_hsa_circ_118587,RMVar_hsa_circ_4060,RMVar_hsa_circ_57346,RMVar_hsa_circ_234727,RMVar_hsa_circ_312126,RMVar_hsa_circ_350683,RMVar_hsa_circ_234729,RMVar_hsa_circ_108735,RMVar_hsa_circ_44785,RMVar_hsa_circ_234730 51418 RMVar_ID_51418 Human_SNP_ID_253095977 A-to-I Human chr5 - 137981710 137981710 137981710 ACAGTCTCGGCACAGTACAGCCTCTGCCCCCCAGGTTCAAGCCATTCTCCTGCCTCAGCCTCCCA ACAGTCTCGGCACAGTACAGCCTCTGCCCCCCCGGTTCAAGCCATTCTCCTGCCTCAGCCTCCCA T G FAM13B Ensembl:ENSG00000031003 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1345990053 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15310179 RMVar_hsa_circ_16545,RMVar_hsa_circ_2085,RMVar_hsa_circ_112333,RMVar_hsa_circ_30640,RMVar_hsa_circ_234704,RMVar_hsa_circ_234711,RMVar_hsa_circ_25179,RMVar_hsa_circ_101914,RMVar_hsa_circ_234712,RMVar_hsa_circ_351149,RMVar_hsa_circ_312134,RMVar_hsa_circ_22020,RMVar_hsa_circ_15172,RMVar_hsa_circ_234714,RMVar_hsa_circ_234715,RMVar_hsa_circ_370360,RMVar_hsa_circ_31307,RMVar_hsa_circ_285318,RMVar_hsa_circ_234719,RMVar_hsa_circ_308204,RMVar_hsa_circ_298525,RMVar_hsa_circ_94237,RMVar_hsa_circ_87011,RMVar_hsa_circ_234721,RMVar_hsa_circ_234722,RMVar_hsa_circ_234720,RMVar_hsa_circ_18365,RMVar_hsa_circ_76620,RMVar_hsa_circ_234725,RMVar_hsa_circ_234726,RMVar_hsa_circ_118587,RMVar_hsa_circ_4060,RMVar_hsa_circ_57346,RMVar_hsa_circ_234727,RMVar_hsa_circ_312126,RMVar_hsa_circ_350683,RMVar_hsa_circ_234729,RMVar_hsa_circ_108735,RMVar_hsa_circ_44785,RMVar_hsa_circ_234730 51419 RMVar_ID_51419 Human_SNP_ID_253097343 A-to-I Human chr5 - 137986840 137986840 137986840 TTTGAGCATTTTAGATTTTGGATTTTCAGATTAGGGATGCCAGTCTGGCACCTCTCCTTGGGATG TTTGAGCATTTTAGATTTTGGATTTTCAGATTGGGGATGCCAGTCTGGCACCTCTCCTTGGGATG T C FAM13B Ensembl:ENSG00000031003 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs981083712 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17575488 RMVar_hsa_circ_16545,RMVar_hsa_circ_2085,RMVar_hsa_circ_112333,RMVar_hsa_circ_30640,RMVar_hsa_circ_234704,RMVar_hsa_circ_234711,RMVar_hsa_circ_25179,RMVar_hsa_circ_101914,RMVar_hsa_circ_234712,RMVar_hsa_circ_351149,RMVar_hsa_circ_312134,RMVar_hsa_circ_22020,RMVar_hsa_circ_15172,RMVar_hsa_circ_234714,RMVar_hsa_circ_234715,RMVar_hsa_circ_370360,RMVar_hsa_circ_31307,RMVar_hsa_circ_285318,RMVar_hsa_circ_234719,RMVar_hsa_circ_308204,RMVar_hsa_circ_298525,RMVar_hsa_circ_94237,RMVar_hsa_circ_87011,RMVar_hsa_circ_234721,RMVar_hsa_circ_234722,RMVar_hsa_circ_234720,RMVar_hsa_circ_18365,RMVar_hsa_circ_234726,RMVar_hsa_circ_118587,RMVar_hsa_circ_234734,RMVar_hsa_circ_290718,RMVar_hsa_circ_4060,RMVar_hsa_circ_57346,RMVar_hsa_circ_234727,RMVar_hsa_circ_312126,RMVar_hsa_circ_350683,RMVar_hsa_circ_234729,RMVar_hsa_circ_108735,RMVar_hsa_circ_44785,RMVar_hsa_circ_234730,RMVar_hsa_circ_309027,RMVar_hsa_circ_325518,RMVar_hsa_circ_334600,RMVar_hsa_circ_306820,RMVar_hsa_circ_46659,RMVar_hsa_circ_279353,RMVar_hsa_circ_284812,RMVar_hsa_circ_234736,RMVar_hsa_circ_234738,RMVar_hsa_circ_234737,RMVar_hsa_circ_234735,RMVar_hsa_circ_234732,RMVar_hsa_circ_234733,RMVar_hsa_circ_234731 51420 RMVar_ID_51420 Human_SNP_ID_253098519 A-to-I Human chr5 - 137992094 137992094 137992094 CAGCCTGGGCAACATGATGAAACCCTGCCTCTACAAAAATTACAAAAGTTAGCTGGGCATGTGCC CAGCCTGGGCAACATGATGAAACCCTGCCTCTGCAAAAATTACAAAAGTTAGCTGGGCATGTGCC T C FAM13B Ensembl:ENSG00000031003 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs972840223 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_30640,RMVar_hsa_circ_234711,RMVar_hsa_circ_351149,RMVar_hsa_circ_312134,RMVar_hsa_circ_22020,RMVar_hsa_circ_15172,RMVar_hsa_circ_234714,RMVar_hsa_circ_234715,RMVar_hsa_circ_31307,RMVar_hsa_circ_285318,RMVar_hsa_circ_308204,RMVar_hsa_circ_298525,RMVar_hsa_circ_234721,RMVar_hsa_circ_234720,RMVar_hsa_circ_18365,RMVar_hsa_circ_118587,RMVar_hsa_circ_234734,RMVar_hsa_circ_290718,RMVar_hsa_circ_57346,RMVar_hsa_circ_234727,RMVar_hsa_circ_312126,RMVar_hsa_circ_108735,RMVar_hsa_circ_234730,RMVar_hsa_circ_309027,RMVar_hsa_circ_334600,RMVar_hsa_circ_306820,RMVar_hsa_circ_46659,RMVar_hsa_circ_284812,RMVar_hsa_circ_234736,RMVar_hsa_circ_234735,RMVar_hsa_circ_234732,RMVar_hsa_circ_234733,RMVar_hsa_circ_234731 51421 RMVar_ID_51421 Human_SNP_ID_253099563 A-to-I Human chr5 - 137996730 137996730 137996730 AAAATTAGCTGAGCATGTTGGTGAGCGCCTGTAATCCCAGCTACTCGGGAGGGTGAGGCAGGAGA AAAATTAGCTGAGCATGTTGGTGAGCGCCTGTCATCCCAGCTACTCGGGAGGGTGAGGCAGGAGA T G FAM13B Ensembl:ENSG00000031003 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs904035240 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25858856 RMVar_hsa_circ_30640,RMVar_hsa_circ_234711,RMVar_hsa_circ_351149,RMVar_hsa_circ_312134,RMVar_hsa_circ_22020,RMVar_hsa_circ_15172,RMVar_hsa_circ_234714,RMVar_hsa_circ_234715,RMVar_hsa_circ_31307,RMVar_hsa_circ_285318,RMVar_hsa_circ_308204,RMVar_hsa_circ_298525,RMVar_hsa_circ_234721,RMVar_hsa_circ_234720,RMVar_hsa_circ_18365,RMVar_hsa_circ_118587,RMVar_hsa_circ_234734,RMVar_hsa_circ_290718,RMVar_hsa_circ_57346,RMVar_hsa_circ_234727,RMVar_hsa_circ_312126,RMVar_hsa_circ_108735,RMVar_hsa_circ_234730,RMVar_hsa_circ_309027,RMVar_hsa_circ_334600,RMVar_hsa_circ_306820,RMVar_hsa_circ_46659,RMVar_hsa_circ_284812,RMVar_hsa_circ_234735,RMVar_hsa_circ_234732,RMVar_hsa_circ_234733,RMVar_hsa_circ_234731 51422 RMVar_ID_51422 Human_SNP_ID_253099593 A-to-I Human chr5 - 137996845 137996845 137996845 CTCATGCCAGTAATCCAGCACTTTGTGAGGCCAAGGAGGGTGGATCACGAGGTCATCAGGAGTTC CTCATGCCAGTAATCCAGCACTTTGTGAGGCCGAGGAGGGTGGATCACGAGGTCATCAGGAGTTC T C FAM13B Ensembl:ENSG00000031003 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1374461994 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_30640,RMVar_hsa_circ_234711,RMVar_hsa_circ_351149,RMVar_hsa_circ_312134,RMVar_hsa_circ_22020,RMVar_hsa_circ_15172,RMVar_hsa_circ_234714,RMVar_hsa_circ_234715,RMVar_hsa_circ_31307,RMVar_hsa_circ_285318,RMVar_hsa_circ_308204,RMVar_hsa_circ_298525,RMVar_hsa_circ_234721,RMVar_hsa_circ_234720,RMVar_hsa_circ_18365,RMVar_hsa_circ_118587,RMVar_hsa_circ_234734,RMVar_hsa_circ_290718,RMVar_hsa_circ_57346,RMVar_hsa_circ_234727,RMVar_hsa_circ_312126,RMVar_hsa_circ_108735,RMVar_hsa_circ_234730,RMVar_hsa_circ_309027,RMVar_hsa_circ_334600,RMVar_hsa_circ_306820,RMVar_hsa_circ_46659,RMVar_hsa_circ_284812,RMVar_hsa_circ_234735,RMVar_hsa_circ_234732,RMVar_hsa_circ_234733,RMVar_hsa_circ_234731 51423 RMVar_ID_51423 Human_SNP_ID_253100920 A-to-I Human chr5 - 138002273 138002273 138002273 CCACCCGTCTCGGCCTTTCAAAGTGTTGGGATAACAGGTGTGAGCCACTGCACCCAACTTCCATT CCACCCGTCTCGGCCTTTCAAAGTGTTGGGATGACAGGTGTGAGCCACTGCACCCAACTTCCATT T C FAM13B Ensembl:ENSG00000031003 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs932088189 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_30640,RMVar_hsa_circ_234711,RMVar_hsa_circ_351149,RMVar_hsa_circ_312134,RMVar_hsa_circ_22020,RMVar_hsa_circ_15172,RMVar_hsa_circ_234714,RMVar_hsa_circ_234715,RMVar_hsa_circ_31307,RMVar_hsa_circ_285318,RMVar_hsa_circ_308204,RMVar_hsa_circ_298525,RMVar_hsa_circ_234721,RMVar_hsa_circ_234720,RMVar_hsa_circ_18365,RMVar_hsa_circ_118587,RMVar_hsa_circ_234734,RMVar_hsa_circ_290718,RMVar_hsa_circ_57346,RMVar_hsa_circ_234727,RMVar_hsa_circ_312126,RMVar_hsa_circ_108735,RMVar_hsa_circ_234730,RMVar_hsa_circ_309027,RMVar_hsa_circ_334600,RMVar_hsa_circ_306820,RMVar_hsa_circ_46659,RMVar_hsa_circ_284812,RMVar_hsa_circ_234735,RMVar_hsa_circ_234732,RMVar_hsa_circ_234733,RMVar_hsa_circ_234731 51424 RMVar_ID_51424 Human_SNP_ID_253139608 A-to-I Human chr5 - 138162333 138162333 138162333 AAAATTAGCTGGGCATGGTGGTATGCACCTATAGTCCCAGCTACTTGGGAGGCTGAGGTGAGAGG AAAATTAGCTGGGCATGGTGGTATGCACCTATTGTCCCAGCTACTTGGGAGGCTGAGGTGAGAGG T A BRD8 Ensembl:ENSG00000112983 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879609634 Functional Loss SNV dbSNP153 33..33 33 - - - 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 51425 RMVar_ID_51425 Human_SNP_ID_253139609 A-to-I Human chr5 - 138162333 138162333 138162333 AAAATTAGCTGGGCATGGTGGTATGCACCTATAGTCCCAGCTACTTGGGAGGCTGAGGTGAGAGG AAAATTAGCTGGGCATGGTGGTATGCACCTATCGTCCCAGCTACTTGGGAGGCTGAGGTGAGAGG T G BRD8 Ensembl:ENSG00000112983 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879609634 Functional Loss SNV dbSNP153 33..33 33 - - - 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 51426 RMVar_ID_51426 Human_SNP_ID_253139657 A-to-I Human chr5 - 138162624 138162624 138162624 GTGGTCCAGTCTGGTCTTGAACTCCTGACCTCAAGCAGTCTTCTTGCCTTGACCTCCCAAAGCAG GTGGTCCAGTCTGGTCTTGAACTCCTGACCTCCAGCAGTCTTCTTGCCTTGACCTCCCAAAGCAG T G BRD8 Ensembl:ENSG00000112983 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1438240344 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15311316 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 51427 RMVar_ID_51427 Human_SNP_ID_253139663 A-to-I Human chr5 - 138162658 138162658 138162658 TTTTAAAAAAATTTTTTTAAGGGACAGGATCTATGTGGTCCAGTCTGGTCTTGAACTCCTGACCT TTTTAAAAAAATTTTTTTAAGGGACAGGATCTGTGTGGTCCAGTCTGGTCTTGAACTCCTGACCT T C BRD8 Ensembl:ENSG00000112983 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs544623793 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15311316,Human_RBP_ID_25859127 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 51428 RMVar_ID_51428 Human_SNP_ID_253139711 A-to-I Human chr5 - 138162814 138162814 138162814 AAAAATTTTTTTAGTAGAAACCAAGTTTTGCTACATTGCCCAGGCTGGTCTCAAACTCCTGAGCT AAAAATTTTTTTAGTAGAAACCAAGTTTTGCTGCATTGCCCAGGCTGGTCTCAAACTCCTGAGCT T C BRD8 Ensembl:ENSG00000112983 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs903497528 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25859130 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 51429 RMVar_ID_51429 Human_SNP_ID_253143410 A-to-I Human chr5 - 138176350 138176350 138176350 GTCTTGAAGTAATGCACCAGTCCTGGCCTCCAAAAGTGCTGGGATTACAAGTGTGAGCCACCATA GTCTTGAAGTAATGCACCAGTCCTGGCCTCCAGAAGTGCTGGGATTACAAGTGTGAGCCACCATA T C BRD8 Ensembl:ENSG00000112983 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1456742265 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35412,RMVar_hsa_circ_53438 51430 RMVar_ID_51430 Human_SNP_ID_253149932 A-to-I Human chr5 - 138200296 138200296 138200296 GAAACCATGTCTCTACTGAAAATATAAAAATTAACCAGGTGTGGTTGTGGATGCCTGTAATCCCA GAAACCATGTCTCTACTGAAAATATAAAAATTCACCAGGTGTGGTTGTGGATGCCTGTAATCCCA T G CDC23 Ensembl:ENSG00000094880 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1306862214 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25859329 RMVar_hsa_circ_60885,RMVar_hsa_circ_266747,RMVar_hsa_circ_267609,RMVar_hsa_circ_274894,RMVar_hsa_circ_334584,RMVar_hsa_circ_55820,RMVar_hsa_circ_28160,RMVar_hsa_circ_234765,RMVar_hsa_circ_33252,RMVar_hsa_circ_290488,RMVar_hsa_circ_337934,RMVar_hsa_circ_57525,RMVar_hsa_circ_294055,RMVar_hsa_circ_234768,RMVar_hsa_circ_234769,RMVar_hsa_circ_234770 51431 RMVar_ID_51431 Human_SNP_ID_253152477 A-to-I Human chr5 - 138211505 138211505 138211505 GCACCCGTCACCACGCCTGGGTAACTTTTTGTATTTTTAGTAGGGACAGGGTTTCACCCTGTTTA GCACCCGTCACCACGCCTGGGTAACTTTTTGTGTTTTTAGTAGGGACAGGGTTTCACCCTGTTTA T C CDC23 Ensembl:ENSG00000094880 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1018283961 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15312296 RMVar_hsa_circ_267609 51432 RMVar_ID_51432 Human_SNP_ID_253182947 A-to-I Human chr5 + 138336579 138336579 138336579 ATGGTGGCACACCCCTGTAGTTCTAGCTATTCAGGAGGCTGAGATGGAAAGGATTGCTTGAGCCC ATGGTGGCACACCCCTGTAGTTCTAGCTATTCGGGAGGCTGAGATGGAAAGGATTGCTTGAGCCC A G FAM53C Ensembl:ENSG00000120709 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs987149081 Functional Loss SNV dbSNP153 33..33 33 - - - 51433 RMVar_ID_51433 Human_SNP_ID_253191152 A-to-I Human chr5 + 138367759 138367759 138367759 TATCTCAGTGGGGCATGATGGCTCACCCCTGTAATCCCAGCGCTTTGGGAGGCCGAGGCAGGTGG TATCTCAGTGGGGCATGATGGCTCACCCCTGTTATCCCAGCGCTTTGGGAGGCCGAGGCAGGTGG A T KDM3B Ensembl:ENSG00000120733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1471974117 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_166979 51434 RMVar_ID_51434 Human_SNP_ID_253194548 A-to-I Human chr5 + 138382331 138382331 138382331 AAAAATAGCCAGGCCTGATGGTGGGTGCCTGTAATCCCAGCTACTCGGGAGGCCGAGGTGGGAGA AAAAATAGCCAGGCCTGATGGTGGGTGCCTGTGATCCCAGCTACTCGGGAGGCCGAGGTGGGAGA A G KDM3B Ensembl:ENSG00000120733 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1013470918 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_15127,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_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_234792 51435 RMVar_ID_51435 Human_SNP_ID_253200004 A-to-I Human chr5 + 138404408 138404408 138404408 CAGCACTTTGGGAGGCCAAGGTGGGCGGGATCACCTGAGGTCGGGAGTTCGAGACCAACCTGGCC CAGCACTTTGGGAGGCCAAGGTGGGCGGGATCGCCTGAGGTCGGGAGTTCGAGACCAACCTGGCC A G KDM3B Ensembl:ENSG00000120733 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1310866237 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_1915,RMVar_hsa_circ_127068,RMVar_hsa_circ_298118,RMVar_hsa_circ_265165,RMVar_hsa_circ_84712,RMVar_hsa_circ_90641,RMVar_hsa_circ_18866,RMVar_hsa_circ_234782,RMVar_hsa_circ_234780,RMVar_hsa_circ_234781,RMVar_hsa_circ_234779,RMVar_hsa_circ_64879,RMVar_hsa_circ_362319,RMVar_hsa_circ_125062,RMVar_hsa_circ_65067,RMVar_hsa_circ_234794,RMVar_hsa_circ_335250,RMVar_hsa_circ_361717,RMVar_hsa_circ_342036,RMVar_hsa_circ_370618,RMVar_hsa_circ_113575,RMVar_hsa_circ_234805,RMVar_hsa_circ_31463,RMVar_hsa_circ_33123,RMVar_hsa_circ_234799,RMVar_hsa_circ_337146,RMVar_hsa_circ_234798,RMVar_hsa_circ_31718,RMVar_hsa_circ_234802,RMVar_hsa_circ_304280,RMVar_hsa_circ_356085,RMVar_hsa_circ_373518,RMVar_hsa_circ_336048,RMVar_hsa_circ_234807,RMVar_hsa_circ_234804,RMVar_hsa_circ_100746,RMVar_hsa_circ_370558,RMVar_hsa_circ_234806 51436 RMVar_ID_51436 Human_SNP_ID_253207535 A-to-I Human chr5 + 138434149 138434149 138434149 TGTTGGGTGTGTTTCTGCAGTCCCAGCCACTCAGGAGGCTGAGGTGGGAGGATTACTTGAGCCCA TGTTGGGTGTGTTTCTGCAGTCCCAGCCACTCGGGAGGCTGAGGTGGGAGGATTACTTGAGCCCA A G KDM3B Ensembl:ENSG00000120733 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1223078759 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_234802 51437 RMVar_ID_51437 Human_SNP_ID_253216826 A-to-I Human chr5 - 138469157 138469157 138469157 GTACAAAGTAAAATAGAACCACAAAATAATGAACTGCATGTTCATAACATACAAAAATCGCCGCC GTACAAAGTAAAATAGAACCACAAAATAATGACCTGCATGTTCATAACATACAAAAATCGCCGCC T G RF00017-4575 RNACentral:URS0000918622 SRP RNA intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1480969495 Functional Loss SNV dbSNP153 33..33 33 - - - 51438 RMVar_ID_51438 Human_SNP_ID_253230810 A-to-I Human chr5 - 138524436 138524436 138524436 TAATTCTCCCACCTCAGTCTCCCAAGTAGCTGAGATTACAGGCACATACCACCATACTTGCCTAA TAATTCTCCCACCTCAGTCTCCCAAGTAGCTGGGATTACAGGCACATACCACCATACTTGCCTAA T C ETF1 Ensembl:ENSG00000120705 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1359014914 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23191946 RMVar_hsa_circ_9281,RMVar_hsa_circ_234827,RMVar_hsa_circ_281237,RMVar_hsa_circ_343667,RMVar_hsa_circ_234830 51439 RMVar_ID_51439 Human_SNP_ID_253231540 A-to-I Human chr5 - 138526665 138526665 138526665 GGGCATGATGGTGCATGCCTGTAATCCCAGCTACTCCAGAGGCTGAGGCAGGAGAATTGCTTAAA GGGCATGATGGTGCATGCCTGTAATCCCAGCTGCTCCAGAGGCTGAGGCAGGAGAATTGCTTAAA T C ETF1 Ensembl:ENSG00000120705 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1230439898 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9281,RMVar_hsa_circ_234827,RMVar_hsa_circ_281237,RMVar_hsa_circ_343667,RMVar_hsa_circ_234830 51440 RMVar_ID_51440 Human_SNP_ID_253232126 A-to-I Human chr5 - 138529090 138529090 138529090 GAGTCTCGCTCTGTCACCCAGGCTGTAGTGCAATGGCGGGATCTTGGCTCACTGCAACCTCTGCC GAGTCTCGCTCTGTCACCCAGGCTGTAGTGCAGTGGCGGGATCTTGGCTCACTGCAACCTCTGCC T C ETF1 Ensembl:ENSG00000120705 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs190591590 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_9281,RMVar_hsa_circ_234827,RMVar_hsa_circ_281237,RMVar_hsa_circ_343667,RMVar_hsa_circ_234830 51441 RMVar_ID_51441 Human_SNP_ID_253232304 A-to-I Human chr5 - 138529831 138529831 138529831 GAGGATCACTTGAACCCAGGAGTTTCCAGGTTACAGTGAGCTGTGATTGTGCCACTGCACTCCAG GAGGATCACTTGAACCCAGGAGTTTCCAGGTTGCAGTGAGCTGTGATTGTGCCACTGCACTCCAG T C ETF1 Ensembl:ENSG00000120705 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1288675064 Functional Loss SNV dbSNP153 33..33 33 - - - 51442 RMVar_ID_51442 Human_SNP_ID_253232338 A-to-I Human chr5 - 138529969 138529968 138529970 TGAGTCTGAGGTGGGAGGAGTGTTTGGGCCCAAGAGTTCGTGACCAGCCTGGGCAGCCTTGTGAG TGAGTCTGAGGTGGGAGGAGTGTTTGGGCCC__GAGTTCGTGACCAGCCTGGGCAGCCTTGTGAG CTT C ETF1 Ensembl:ENSG00000120705 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs983198245 Functional Loss DEL dbSNP153 32..33 33 - - - Human_RBP_ID_7390010,Human_RBP_ID_15314635 51443 RMVar_ID_51443 Human_SNP_ID_253232467 A-to-I Human chr5 - 138530429 138530429 138530429 TACTAAAAATACAACAATTAGCTGGGCGTGGTAGTGGGCGCCTGTATCCCAGCTACTTGGGAGGC TACTAAAAATACAACAATTAGCTGGGCGTGGTGGTGGGCGCCTGTATCCCAGCTACTTGGGAGGC T C ETF1 Ensembl:ENSG00000120705 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1304264822 Functional Loss SNV dbSNP153 33..33 33 - - - 51444 RMVar_ID_51444 Human_SNP_ID_253232497 A-to-I Human chr5 - 138530544 138530544 138530544 GCTGGGTGCGGTGGCTAAAGCCTGTAATCCCAACACTTTGGGAGACTGAGGTGGGTGGATAATTT GCTGGGTGCGGTGGCTAAAGCCTGTAATCCCAGCACTTTGGGAGACTGAGGTGGGTGGATAATTT T C ETF1 Ensembl:ENSG00000120705 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs868779753 Functional Loss SNV dbSNP153 33..33 33 - - - 51445 RMVar_ID_51445 Human_SNP_ID_253233305 A-to-I Human chr5 - 138533564 138533564 138533564 CTTCTGCCTCAGACTCCCAAGTAACTGGTACTACAGGTGCGTGCCACCACATCCAGCTAAGTTTT CTTCTGCCTCAGACTCCCAAGTAACTGGTACTGCAGGTGCGTGCCACCACATCCAGCTAAGTTTT T C ETF1 Ensembl:ENSG00000120705 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs112622059 Functional Loss SNV dbSNP153 33..33 33 - - - 51446 RMVar_ID_51446 Human_SNP_ID_253233900 A-to-I Human chr5 - 138535823 138535823 138535823 CCGCCCAGGCTTGAGTGCAGTGGTGCGATCTCAGCTTACTGCAACCTCCACCTCCCAGGTTCAGC CCGCCCAGGCTTGAGTGCAGTGGTGCGATCTCGGCTTACTGCAACCTCCACCTCCCAGGTTCAGC T C ETF1 Ensembl:ENSG00000120705 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs572851013 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15314789 51447 RMVar_ID_51447 Human_SNP_ID_253237919 A-to-I Human chr5 + 138550511 138550511 138550511 AAAATTAGCCGGGCATGGTGGCGGGCGCTTGTAGTCACAGCTACTCGGGAGGCTGAGGGAGGAGA AAAATTAGCCGGGCATGGTGGCGGGCGCTTGTCGTCACAGCTACTCGGGAGGCTGAGGGAGGAGA A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1313426132 Functional Loss SNV dbSNP153 33..33 33 - - - 51448 RMVar_ID_51448 Human_SNP_ID_253242263 A-to-I Human chr5 - 138565790 138565790 138565790 AGGATTGTTTGAGCCCAGGAGGTTGAGGCTGCAGTGAGCCGTGATCACACCATTTCACTCCAGCC AGGATTGTTTGAGCCCAGGAGGTTGAGGCTGCCGTGAGCCGTGATCACACCATTTCACTCCAGCC T G HSPA9 Ensembl:ENSG00000113013 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1048971698 Functional Loss SNV dbSNP153 33..33 33 - - - 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 51449 RMVar_ID_51449 Human_SNP_ID_253242355 A-to-I Human chr5 - 138566149 138566149 138566149 AGTTTTGCTCCTGTTGCCCAGGCTACAGTGCAATGGCGTGATCTTGGCTCACCGCAACCTCTGCC AGTTTTGCTCCTGTTGCCCAGGCTACAGTGCAGTGGCGTGATCTTGGCTCACCGCAACCTCTGCC T C HSPA9 Ensembl:ENSG00000113013 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs560647931 Functional Loss SNV dbSNP153 33..33 33 - - - 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 51450 RMVar_ID_51450 Human_SNP_ID_253243573 A-to-I Human chr5 - 138570146 138570146 138570146 ATAGACATACTAGAGGCTCGGTGGGGTGACTCACACCTGTAATCCTAACACTTTGGGAGGCTGAG ATAGACATACTAGAGGCTCGGTGGGGTGACTCCCACCTGTAATCCTAACACTTTGGGAGGCTGAG T G HSPA9 Ensembl:ENSG00000113013 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1272927981 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_249896,Human_RBP_ID_17575763 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_375775,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_28140,RMVar_hsa_circ_359269,RMVar_hsa_circ_234848,RMVar_hsa_circ_350924,RMVar_hsa_circ_234850,RMVar_hsa_circ_366090,RMVar_hsa_circ_375990,RMVar_hsa_circ_234851,RMVar_hsa_circ_234855,RMVar_hsa_circ_271001,RMVar_hsa_circ_329131,RMVar_hsa_circ_364235,RMVar_hsa_circ_234856,RMVar_hsa_circ_234854 51451 RMVar_ID_51451 Human_SNP_ID_253243593 A-to-I Human chr5 - 138570227 138570227 138570227 CAACTGACCCTTCCACCCCAGCCTCCCAAATTATTGGGATTACAGGCGTGAGCCACCATGCCCAG CAACTGACCCTTCCACCCCAGCCTCCCAAATTGTTGGGATTACAGGCGTGAGCCACCATGCCCAG T C HSPA9 Ensembl:ENSG00000113013 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1019916363 Functional Loss SNV dbSNP153 33..33 33 - - - 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_375775,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_28140,RMVar_hsa_circ_359269,RMVar_hsa_circ_234848,RMVar_hsa_circ_350924,RMVar_hsa_circ_234850,RMVar_hsa_circ_366090,RMVar_hsa_circ_375990,RMVar_hsa_circ_234851,RMVar_hsa_circ_234855,RMVar_hsa_circ_271001,RMVar_hsa_circ_329131,RMVar_hsa_circ_364235,RMVar_hsa_circ_234856,RMVar_hsa_circ_234854 51452 RMVar_ID_51452 Human_SNP_ID_253243596 A-to-I Human chr5 - 138570231 138570231 138570231 GACTCAACTGACCCTTCCACCCCAGCCTCCCAAATTATTGGGATTACAGGCGTGAGCCACCATGC GACTCAACTGACCCTTCCACCCCAGCCTCCCAGATTATTGGGATTACAGGCGTGAGCCACCATGC T C HSPA9 Ensembl:ENSG00000113013 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs760802627 Functional Loss SNV dbSNP153 33..33 33 - - - 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_375775,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_28140,RMVar_hsa_circ_359269,RMVar_hsa_circ_234848,RMVar_hsa_circ_350924,RMVar_hsa_circ_234850,RMVar_hsa_circ_366090,RMVar_hsa_circ_375990,RMVar_hsa_circ_234851,RMVar_hsa_circ_234855,RMVar_hsa_circ_271001,RMVar_hsa_circ_329131,RMVar_hsa_circ_364235,RMVar_hsa_circ_234856,RMVar_hsa_circ_234854 51453 RMVar_ID_51453 Human_SNP_ID_253243597 A-to-I Human chr5 - 138570231 138570231 138570231 GACTCAACTGACCCTTCCACCCCAGCCTCCCAAATTATTGGGATTACAGGCGTGAGCCACCATGC GACTCAACTGACCCTTCCACCCCAGCCTCCCACATTATTGGGATTACAGGCGTGAGCCACCATGC T G HSPA9 Ensembl:ENSG00000113013 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs760802627 Functional Loss SNV dbSNP153 33..33 33 - - - 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_375775,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_28140,RMVar_hsa_circ_359269,RMVar_hsa_circ_234848,RMVar_hsa_circ_350924,RMVar_hsa_circ_234850,RMVar_hsa_circ_366090,RMVar_hsa_circ_375990,RMVar_hsa_circ_234851,RMVar_hsa_circ_234855,RMVar_hsa_circ_271001,RMVar_hsa_circ_329131,RMVar_hsa_circ_364235,RMVar_hsa_circ_234856,RMVar_hsa_circ_234854 51454 RMVar_ID_51454 Human_SNP_ID_253243603 A-to-I Human chr5 - 138570282 138570281 138570282 CCCAATAGAAACGGGGCTCACTATGTTGCCCAAGTTGGTGTTGAACTCCTGGACTCAACTGACCC CCCAATAGAAACGGGGCTCACTATGTTGCCCA_GTTGGTGTTGAACTCCTGGACTCAACTGACCC CT C HSPA9 Ensembl:ENSG00000113013 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1182803045 Functional Loss DEL dbSNP153 33..33 33 - - - 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_375775,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_28140,RMVar_hsa_circ_359269,RMVar_hsa_circ_234848,RMVar_hsa_circ_350924,RMVar_hsa_circ_234850,RMVar_hsa_circ_366090,RMVar_hsa_circ_375990,RMVar_hsa_circ_234851,RMVar_hsa_circ_234855,RMVar_hsa_circ_271001,RMVar_hsa_circ_329131,RMVar_hsa_circ_364235,RMVar_hsa_circ_234856,RMVar_hsa_circ_234854 51455 RMVar_ID_51455 Human_SNP_ID_253243605 A-to-I Human chr5 - 138570295 138570292 138570296 TTTCTTCCCCCCTCCCAATAGAAACGGGGCTCACTATGTTGCCCAAGTTGGTGTTGAACTCCTGG TTTCTTCCCCCCTCCCAATAGAAACGGGGCT____ATGTTGCCCAAGTTGGTGTTGAACTCCTGG TAGTG T HSPA9 Ensembl:ENSG00000113013 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924481983 Functional Loss DEL dbSNP153 32..35 33 - - - 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_375775,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_28140,RMVar_hsa_circ_359269,RMVar_hsa_circ_234848,RMVar_hsa_circ_350924,RMVar_hsa_circ_234850,RMVar_hsa_circ_366090,RMVar_hsa_circ_375990,RMVar_hsa_circ_234851,RMVar_hsa_circ_234855,RMVar_hsa_circ_271001,RMVar_hsa_circ_329131,RMVar_hsa_circ_364235,RMVar_hsa_circ_234856,RMVar_hsa_circ_234854 51456 RMVar_ID_51456 Human_SNP_ID_253243606 A-to-I Human chr5 - 138570292 138570292 138570292 CTTCCCCCCTCCCAATAGAAACGGGGCTCACTATGTTGCCCAAGTTGGTGTTGAACTCCTGGACT CTTCCCCCCTCCCAATAGAAACGGGGCTCACTGTGTTGCCCAAGTTGGTGTTGAACTCCTGGACT T C HSPA9 Ensembl:ENSG00000113013 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs977332750 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4811836 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_375775,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_28140,RMVar_hsa_circ_359269,RMVar_hsa_circ_234848,RMVar_hsa_circ_350924,RMVar_hsa_circ_234850,RMVar_hsa_circ_366090,RMVar_hsa_circ_375990,RMVar_hsa_circ_234851,RMVar_hsa_circ_234855,RMVar_hsa_circ_271001,RMVar_hsa_circ_329131,RMVar_hsa_circ_364235,RMVar_hsa_circ_234856,RMVar_hsa_circ_234854 51457 RMVar_ID_51457 Human_SNP_ID_253244613 A-to-I Human chr5 - 138573460 138573460 138573460 TTTTCAGTAGAGACAGTTCCACTGTGTTGGCCAGGCTGGTCTTGAGCTCAAGTGATCCGCCCACG TTTTCAGTAGAGACAGTTCCACTGTGTTGGCCGGGCTGGTCTTGAGCTCAAGTGATCCGCCCACG T C HSPA9 Ensembl:ENSG00000113013 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893460172 Functional Loss SNV dbSNP153 33..33 33 - - - 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 51458 RMVar_ID_51458 Human_SNP_ID_253244614 A-to-I Human chr5 - 138573460 138573460 138573460 TTTTCAGTAGAGACAGTTCCACTGTGTTGGCCAGGCTGGTCTTGAGCTCAAGTGATCCGCCCACG TTTTCAGTAGAGACAGTTCCACTGTGTTGGCCCGGCTGGTCTTGAGCTCAAGTGATCCGCCCACG T G HSPA9 Ensembl:ENSG00000113013 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs893460172 Functional Loss SNV dbSNP153 33..33 33 - - - 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 51459 RMVar_ID_51459 Human_SNP_ID_253244620 A-to-I Human chr5 - 138573478 138573478 138573478 CCTGGCTAATTTTTTGTATTTTCAGTAGAGACAGTTCCACTGTGTTGGCCAGGCTGGTCTTGAGC CCTGGCTAATTTTTTGTATTTTCAGTAGAGACCGTTCCACTGTGTTGGCCAGGCTGGTCTTGAGC T G HSPA9 Ensembl:ENSG00000113013 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1158561924 Functional Loss SNV dbSNP153 33..33 33 - - - 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 51460 RMVar_ID_51460 Human_SNP_ID_253244627 A-to-I Human chr5 - 138573502 138573502 138573502 GGATTACAGGCATGAACCACCATTCCTGGCTAATTTTTTGTATTTTCAGTAGAGACAGTTCCACT GGATTACAGGCATGAACCACCATTCCTGGCTATTTTTTTGTATTTTCAGTAGAGACAGTTCCACT T A HSPA9 Ensembl:ENSG00000113013 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1010604463 Functional Loss SNV dbSNP153 33..33 33 - - - 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 51461 RMVar_ID_51461 Human_SNP_ID_253244641 A-to-I Human chr5 - 138573565 138573565 138573565 TCCGCTCACTGCAACCTCTGCCTCCTGGGTTCAAACAGTTCTCCTGCCTTGGCCACATAGCTGGG TCCGCTCACTGCAACCTCTGCCTCCTGGGTTCTAACAGTTCTCCTGCCTTGGCCACATAGCTGGG T A HSPA9 Ensembl:ENSG00000113013 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1417001095 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23313789 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 51462 RMVar_ID_51462 Human_SNP_ID_253281312 A-to-I Human chr5 + 138724299 138724299 138724299 AAAATTGGCTGGGCGTGGTGGCGCGCGCCTGTAGTCCCAGCTGATCGGGAGGCTGAGGCAGGAGA AAAATTGGCTGGGCGTGGTGGCGCGCGCCTGTGGTCCCAGCTGATCGGGAGGCTGAGGCAGGAGA A G CTNNA1 Ensembl:ENSG00000044115 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1235344235 Functional Loss SNV dbSNP153 33..33 33 - - - 51463 RMVar_ID_51463 Human_SNP_ID_253290729 A-to-I Human chr5 + 138761945 138761944 138761946 GCCTGGCTAATTTTTGTGTTTTCTGTAGAGACAGAGTTTCACCGTGTTTCCCAGGCTGGTCTCAA GCCTGGCTAATTTTTGTGTTTTCTGTAGAGAC__AGTTTCACCGTGTTTCCCAGGCTGGTCTCAA CAG C CTNNA1 Ensembl:ENSG00000044115 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs975935763 Functional Loss DEL dbSNP153 33..34 33 - - - Human_Splice_Rec_697016 51464 RMVar_ID_51464 Human_SNP_ID_253291082 A-to-I Human chr5 + 138763527 138763527 138763527 ACGACACCCAGCTAATTTTTTACATTTTTAGTAGAGACAGGTCTCACCATATTGCTTAGGCTGAT ACGACACCCAGCTAATTTTTTACATTTTTAGTGGAGACAGGTCTCACCATATTGCTTAGGCTGAT A G CTNNA1 Ensembl:ENSG00000044115 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs932467701 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15315873 51465 RMVar_ID_51465 Human_SNP_ID_253291085 A-to-I Human chr5 + 138763545 138763545 138763545 TTTACATTTTTAGTAGAGACAGGTCTCACCATATTGCTTAGGCTGATCTTTGAACTCCTGAACTC TTTACATTTTTAGTAGAGACAGGTCTCACCATGTTGCTTAGGCTGATCTTTGAACTCCTGAACTC A G CTNNA1 Ensembl:ENSG00000044115 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs542839614 Functional Loss SNV dbSNP153 33..33 33 - - - 51466 RMVar_ID_51466 Human_SNP_ID_253291190 A-to-I Human chr5 + 138764020 138764020 138764020 TAGCCTGACTAACATGGAGAAACACCGTCTCTACTAAAAATACAAAAAATTGCAGGGCGCGGTGT TAGCCTGACTAACATGGAGAAACACCGTCTCTGCTAAAAATACAAAAAATTGCAGGGCGCGGTGT A G CTNNA1 Ensembl:ENSG00000044115 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs980873944 Functional Loss SNV dbSNP153 33..33 33 - - - 51467 RMVar_ID_51467 Human_SNP_ID_253295489 A-to-I Human chr5 + 138778133 138778133 138778133 CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGACCGCCACCACGCCCGGCTAATTTTT CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTCCAGGCGACCGCCACCACGCCCGGCTAATTTTT A C CTNNA1 Ensembl:ENSG00000044115 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1217888292 Functional Loss SNV dbSNP153 33..33 33 - - - 51468 RMVar_ID_51468 Human_SNP_ID_253295522 A-to-I Human chr5 + 138778205 138778205 138778205 TTTAGTAGAGACGGGGTTTCACAGTGTTGACCAGGATGGTTTCGATCTCCTGAACTCGTGATCCA TTTAGTAGAGACGGGGTTTCACAGTGTTGACCGGGATGGTTTCGATCTCCTGAACTCGTGATCCA A G CTNNA1 Ensembl:ENSG00000044115 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1167558562 Functional Loss SNV dbSNP153 33..33 33 - - - 51469 RMVar_ID_51469 Human_SNP_ID_253296482 A-to-I Human chr5 + 138781435 138781435 138781435 AAAATTAGCCGGGCGTGGTGGCGGGCCCCTGTAGTCACAGCCACTTGGGAGGCTGAGGCCAGAGA AAAATTAGCCGGGCGTGGTGGCGGGCCCCTGTGGTCACAGCCACTTGGGAGGCTGAGGCCAGAGA A G CTNNA1 Ensembl:ENSG00000044115 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1421500570 Functional Loss SNV dbSNP153 33..33 33 - - - 51470 RMVar_ID_51470 Human_SNP_ID_253321151 A-to-I Human chr5 + 138879647 138879646 138879648 CAGCTAATTAAAAAAATTTTTTTCGTGGAGACAGGGTCTCACTATGTTGCCTAGGCTGGTCTCGA CAGCTAATTAAAAAAATTTTTTTCGTGGAGAC__GGTCTCACTATGTTGCCTAGGCTGGTCTCGA CAG C CTNNA1 Ensembl:ENSG00000044115 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1368732865 Functional Loss DEL dbSNP153 33..34 33 - - - 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_327909,RMVar_hsa_circ_328732,RMVar_hsa_circ_116014,RMVar_hsa_circ_234867 51471 RMVar_ID_51471 Human_SNP_ID_253321265 A-to-I Human chr5 + 138880192 138880192 138880192 AGTTTTTGTGTTTGTTCGTTTGTTTTTGAGACAAGGTCTCACTGTGTTGCCCAGGTTGGAGTGCA AGTTTTTGTGTTTGTTCGTTTGTTTTTGAGACGAGGTCTCACTGTGTTGCCCAGGTTGGAGTGCA A G CTNNA1 Ensembl:ENSG00000044115 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1340946601 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_697132,Human_Splice_Rec_697133,Human_Splice_Rec_697147,Human_Splice_Rec_697157,Human_Splice_Rec_697185,Human_Splice_Rec_697199,Human_Splice_Rec_697219,Human_Splice_Rec_697267 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_327909,RMVar_hsa_circ_328732,RMVar_hsa_circ_116014,RMVar_hsa_circ_234867 51472 RMVar_ID_51472 Human_SNP_ID_253321277 A-to-I Human chr5 + 138880275 138880275 138880275 CTCCATTGATCTCCCTCCTTAGCCTCCCAGATAGCTGGGACTACAGGTGCGTACCACCATGCCTG CTCCATTGATCTCCCTCCTTAGCCTCCCAGATGGCTGGGACTACAGGTGCGTACCACCATGCCTG A G CTNNA1 Ensembl:ENSG00000044115 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1390765434 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_697132,Human_Splice_Rec_697133,Human_Splice_Rec_697146,Human_Splice_Rec_697147,Human_Splice_Rec_697156,Human_Splice_Rec_697157,Human_Splice_Rec_697184,Human_Splice_Rec_697185,Human_Splice_Rec_697198,Human_Splice_Rec_697199,Human_Splice_Rec_697218,Human_Splice_Rec_697219,Human_Splice_Rec_697267 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_327909,RMVar_hsa_circ_328732,RMVar_hsa_circ_116014,RMVar_hsa_circ_234867 51473 RMVar_ID_51473 Human_SNP_ID_253336177 A-to-I Human chr5 - 138939685 138939685 138939685 GTCGGGTGTGGTGGCTCATGCCTGTAATCCCAACACTTTGGGAGGCTGAGGTGGGTGGGTCACCT GTCGGGTGTGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGTGGGTCACCT T C RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1051576255 Functional Loss SNV dbSNP153 33..33 33 - - - 51474 RMVar_ID_51474 Human_SNP_ID_253336179 A-to-I Human chr5 - 138939691 138939691 138939691 GTTGAGGTCGGGTGTGGTGGCTCATGCCTGTAATCCCAACACTTTGGGAGGCTGAGGTGGGTGGG GTTGAGGTCGGGTGTGGTGGCTCATGCCTGTAGTCCCAACACTTTGGGAGGCTGAGGTGGGTGGG T C RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1141423 Functional Loss SNV dbSNP153 33..33 33 - - - 51475 RMVar_ID_51475 Human_SNP_ID_253342251 A-to-I Human chr5 - 138965486 138965486 138965486 CAGTAATTAATTGTGCCCCTTTCACTCTCAAAAGTGTCCCGGTTTGGACAATAAATTATGTGGTC CAGTAATTAATTGTGCCCCTTTCACTCTCAAAGGTGTCCCGGTTTGGACAATAAATTATGTGGTC T C SIL1 Ensembl:ENSG00000120725 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1283681569 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102128,RMVar_hsa_circ_234880 51476 RMVar_ID_51476 Human_SNP_ID_253347261 A-to-I Human chr5 - 138988751 138988751 138988751 CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACCACAGGTACGTACCACCATGCCTGGCCAATTTAA CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACCGCAGGTACGTACCACCATGCCTGGCCAATTTAA T C SIL1 Ensembl:ENSG00000120725 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs983217495 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102128,RMVar_hsa_circ_234880 51477 RMVar_ID_51477 Human_SNP_ID_253347262 A-to-I Human chr5 - 138988751 138988751 138988751 CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACCACAGGTACGTACCACCATGCCTGGCCAATTTAA CTCCTGCCTCAGCCTCCCAAGTAGCTGGGACCCCAGGTACGTACCACCATGCCTGGCCAATTTAA T G SIL1 Ensembl:ENSG00000120725 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs983217495 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102128,RMVar_hsa_circ_234880 51478 RMVar_ID_51478 Human_SNP_ID_253349587 A-to-I Human chr5 - 138999546 138999546 138999546 GAAACAATCCTCCTGCCTCCACCTCAGTAGCTAGGACTGCAGGTGTACTCTACCATGCCTGGCTA GAAACAATCCTCCTGCCTCCACCTCAGTAGCTGGGACTGCAGGTGTACTCTACCATGCCTGGCTA T C SIL1 Ensembl:ENSG00000120725 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1330850175 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102128,RMVar_hsa_circ_234880 51479 RMVar_ID_51479 Human_SNP_ID_253349642 A-to-I Human chr5 - 138999811 138999811 138999811 GCACTGCAGCCTTGACCTGCTGGGCTCAAGCAATCTTCCCACCTTAGCCTTCCAAACAACAGATC GCACTGCAGCCTTGACCTGCTGGGCTCAAGCAGTCTTCCCACCTTAGCCTTCCAAACAACAGATC T C SIL1 Ensembl:ENSG00000120725 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1383404739 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102128,RMVar_hsa_circ_234880 51480 RMVar_ID_51480 Human_SNP_ID_253352904 A-to-I Human chr5 - 139012923 139012923 139012923 TTGAGACAGATCTTGCTGTATCACCCAAGCCTAGAGTGCAGTGGTGCAAACACGGCTTACTGCAG TTGAGACAGATCTTGCTGTATCACCCAAGCCTGGAGTGCAGTGGTGCAAACACGGCTTACTGCAG T C SIL1 Ensembl:ENSG00000120725 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs948551045 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102128,RMVar_hsa_circ_234880 51481 RMVar_ID_51481 Human_SNP_ID_253360378 A-to-I Human chr5 - 139048213 139048213 139048213 TGGGGAGGTTGAGGCTGCAATAAGCCGTGATTATGCCACTGTACTGCAGCCTGGGTGACACAGTG TGGGGAGGTTGAGGCTGCAATAAGCCGTGATTCTGCCACTGTACTGCAGCCTGGGTGACACAGTG T G SIL1 Ensembl:ENSG00000120725 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1192591771 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_7892,RMVar_hsa_circ_102128,RMVar_hsa_circ_234880,RMVar_hsa_circ_371391,RMVar_hsa_circ_234883,RMVar_hsa_circ_364209,RMVar_hsa_circ_74863,RMVar_hsa_circ_314904,RMVar_hsa_circ_234886,RMVar_hsa_circ_109245,RMVar_hsa_circ_234887,RMVar_hsa_circ_234888 51482 RMVar_ID_51482 Human_SNP_ID_253393123 A-to-I Human chr5 - 139196013 139196011 139196013 GCTAATTTTGTAATTTTAATTTTTGTAGAGACAGGGTCTCGCTGTGTTGCCCAGGCTGTTTTTGA GCTAATTTTGTAATTTTAATTTTTGTAGAGAC__GGTCTCGCTGTGTTGCCCAGGCTGTTTTTGA CCT C SIL1 Ensembl:ENSG00000120725 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1276333800 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_56379 51483 RMVar_ID_51483 Human_SNP_ID_253413024 A-to-I Human chr5 + 139277159 139277159 139277159 AACCAGATAATTTTTTTTTTTTTAATTTGTAGAGACAAAGTCTCATTATGTTGCCCAGGCTTTAG AACCAGATAATTTTTTTTTTTTTAATTTGTAGGGACAAAGTCTCATTATGTTGCCCAGGCTTTAG A G MATR3,SNHG4 Ensembl:ENSG00000280987,Ensembl:ENSG00000281398 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs544998049 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2899418,Human_RBP_ID_7391358 RMVar_hsa_circ_79765,RMVar_hsa_circ_234891,RMVar_hsa_circ_118220,RMVar_hsa_circ_108264,RMVar_hsa_circ_116622,RMVar_hsa_circ_234890,RMVar_hsa_circ_296173,RMVar_hsa_circ_112055,RMVar_hsa_circ_234892,RMVar_hsa_circ_234894,RMVar_hsa_circ_234895,RMVar_hsa_circ_234893 51484 RMVar_ID_51484 Human_SNP_ID_253413026 A-to-I Human chr5 + 139277163 139277163 139277163 AGATAATTTTTTTTTTTTTAATTTGTAGAGACAAAGTCTCATTATGTTGCCCAGGCTTTAGTAGA AGATAATTTTTTTTTTTTTAATTTGTAGAGACGAAGTCTCATTATGTTGCCCAGGCTTTAGTAGA A G MATR3,SNHG4 Ensembl:ENSG00000280987,Ensembl:ENSG00000281398 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1400591064 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1645758,Human_RBP_ID_7391358 RMVar_hsa_circ_79765,RMVar_hsa_circ_234891,RMVar_hsa_circ_118220,RMVar_hsa_circ_108264,RMVar_hsa_circ_116622,RMVar_hsa_circ_234890,RMVar_hsa_circ_296173,RMVar_hsa_circ_112055,RMVar_hsa_circ_234892,RMVar_hsa_circ_234894,RMVar_hsa_circ_234895,RMVar_hsa_circ_234893 51485 RMVar_ID_51485 Human_SNP_ID_253414506 A-to-I Human chr5 + 139282894 139282894 139282894 GTCATCCAGGCTGGAGTGCAATGTAATGGCTCAATCTCAGCTCACTGCAACCTCTGCCTCCCGGG GTCATCCAGGCTGGAGTGCAATGTAATGGCTCGATCTCAGCTCACTGCAACCTCTGCCTCCCGGG A G MATR3,SNHG4 Ensembl:ENSG00000280987,Ensembl:ENSG00000281398 Protein coding,lincRNA intron,exon GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1189179185 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2899528,Human_RBP_ID_5267708,Human_RBP_ID_15318376 RMVar_hsa_circ_234897,RMVar_hsa_circ_91210,RMVar_hsa_circ_234891,RMVar_hsa_circ_108264,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_94849,RMVar_hsa_circ_79033,RMVar_hsa_circ_85144,RMVar_hsa_circ_89228,RMVar_hsa_circ_234901,RMVar_hsa_circ_234905,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_234911,RMVar_hsa_circ_76654,RMVar_hsa_circ_234912 51486 RMVar_ID_51486 Human_SNP_ID_253414839 A-to-I Human chr5 + 139284349 139284349 139284349 ATGATAATGGATTTGGCCGGGCGCGGTTGCCTATAATCCCAACACTGAGAGGCTGAGGTGGGTGG ATGATAATGGATTTGGCCGGGCGCGGTTGCCTGTAATCCCAACACTGAGAGGCTGAGGTGGGTGG A G MATR3,SNHG4 Ensembl:ENSG00000280987,Ensembl:ENSG00000281398 Protein coding,lincRNA intron,exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs112738841 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_250522,Human_RBP_ID_787271,Human_RBP_ID_2899562,Human_RBP_ID_15318471,Human_RBP_ID_18170504 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 51487 RMVar_ID_51487 Human_SNP_ID_253417949 A-to-I Human chr5 + 139295900 139295900 139295900 TGCAGTGGTATGATCAGTGGCTCACGGCTCACAGCAGCCTCGACCTCCCAGGCTTAAGTAATCCT TGCAGTGGTATGATCAGTGGCTCACGGCTCACGGCAGCCTCGACCTCCCAGGCTTAAGTAATCCT A G MATR3,MATR3:2 Ensembl:ENSG00000280987,Ensembl:ENSG00000015479 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs543686422 Functional Loss SNV dbSNP153 33..33 33 - - - 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_118135,RMVar_hsa_circ_234914 51488 RMVar_ID_51488 Human_SNP_ID_253417950 A-to-I Human chr5 + 139295903 139295903 139295903 AGTGGTATGATCAGTGGCTCACGGCTCACAGCAGCCTCGACCTCCCAGGCTTAAGTAATCCTCCC AGTGGTATGATCAGTGGCTCACGGCTCACAGCGGCCTCGACCTCCCAGGCTTAAGTAATCCTCCC A G MATR3,MATR3:2 Ensembl:ENSG00000280987,Ensembl:ENSG00000015479 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1236854432 Functional Loss SNV dbSNP153 33..33 33 - - - 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_118135,RMVar_hsa_circ_234914 51489 RMVar_ID_51489 Human_SNP_ID_253417954 A-to-I Human chr5 + 139295917 139295917 139295917 TGGCTCACGGCTCACAGCAGCCTCGACCTCCCAGGCTTAAGTAATCCTCCCACCTCAGCCTCCTG TGGCTCACGGCTCACAGCAGCCTCGACCTCCCGGGCTTAAGTAATCCTCCCACCTCAGCCTCCTG A G MATR3,MATR3:2 Ensembl:ENSG00000280987,Ensembl:ENSG00000015479 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1443929320 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15318864,Human_RBP_ID_23039558 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_118135,RMVar_hsa_circ_234914 51490 RMVar_ID_51490 Human_SNP_ID_253417966 A-to-I Human chr5 + 139295963 139295963 139295963 CTCCCACCTCAGCCTCCTGGGTAGCTGAGATCACAGGCGCGCGCCACCACACCAAGCTAATTTTT CTCCCACCTCAGCCTCCTGGGTAGCTGAGATCCCAGGCGCGCGCCACCACACCAAGCTAATTTTT A C MATR3,MATR3:2 Ensembl:ENSG00000280987,Ensembl:ENSG00000015479 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1029585687 Functional Loss SNV dbSNP153 33..33 33 - - - 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_118135,RMVar_hsa_circ_234914 51491 RMVar_ID_51491 Human_SNP_ID_253418963 A-to-I Human chr5 + 139299524 139299524 139299524 AGTGAGACCTTGTCTCTACTAAAAATGTTAAAAATTAGTCGGGTATAGTGGTGCATGCCTGTGGT AGTGAGACCTTGTCTCTACTAAAAATGTTAAACATTAGTCGGGTATAGTGGTGCATGCCTGTGGT A C MATR3,MATR3:2 Ensembl:ENSG00000280987,Ensembl:ENSG00000015479 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1419488488 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9170354,Human_RBP_ID_15319019,Human_RBP_ID_27735450 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_118135,RMVar_hsa_circ_234914 51492 RMVar_ID_51492 Human_SNP_ID_253418964 A-to-I Human chr5 + 139299524 139299524 139299524 AGTGAGACCTTGTCTCTACTAAAAATGTTAAAAATTAGTCGGGTATAGTGGTGCATGCCTGTGGT AGTGAGACCTTGTCTCTACTAAAAATGTTAAATATTAGTCGGGTATAGTGGTGCATGCCTGTGGT A T MATR3,MATR3:2 Ensembl:ENSG00000280987,Ensembl:ENSG00000015479 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1419488488 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9170354,Human_RBP_ID_15319019,Human_RBP_ID_27735450 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_118135,RMVar_hsa_circ_234914 51493 RMVar_ID_51493 Human_SNP_ID_253418967 A-to-I Human chr5 + 139299536 139299536 139299536 TCTCTACTAAAAATGTTAAAAATTAGTCGGGTATAGTGGTGCATGCCTGTGGTCCCTGCTGAGAC TCTCTACTAAAAATGTTAAAAATTAGTCGGGTGTAGTGGTGCATGCCTGTGGTCCCTGCTGAGAC A G MATR3,MATR3:2 Ensembl:ENSG00000280987,Ensembl:ENSG00000015479 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1410104884 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17158533,Human_RBP_ID_24085801,Human_RBP_ID_25861560,Human_RBP_ID_27735450 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_118135,RMVar_hsa_circ_234914 51494 RMVar_ID_51494 Human_SNP_ID_253418981 A-to-I Human chr5 + 139299590 139299590 139299590 CCTGCTGAGACCAAGGAGGATCACTTGAGCCCAAGAGATTGAGTCTGCAATGAGCCAAGATTGTG CCTGCTGAGACCAAGGAGGATCACTTGAGCCCGAGAGATTGAGTCTGCAATGAGCCAAGATTGTG A G MATR3,MATR3:2 Ensembl:ENSG00000280987,Ensembl:ENSG00000015479 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1438738648 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1645807,Human_RBP_ID_1988073,Human_RBP_ID_7391676,Human_RBP_ID_15319021,Human_RBP_ID_17158533,Human_RBP_ID_27735451 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_118135,RMVar_hsa_circ_234914 51495 RMVar_ID_51495 Human_SNP_ID_253419143 A-to-I Human chr5 + 139300222 139300222 139300222 TTGTCTCTACTAAAAAATACAGAAAATTTGCCAGGTGTGGTGGTGTGCACCTGTAACCCCAGCTA TTGTCTCTACTAAAAAATACAGAAAATTTGCCGGGTGTGGTGGTGTGCACCTGTAACCCCAGCTA A G MATR3,MATR3:2 Ensembl:ENSG00000280987,Ensembl:ENSG00000015479 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs936880822 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15319055,Human_RBP_ID_22727719 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_118135,RMVar_hsa_circ_234914 51496 RMVar_ID_51496 Human_SNP_ID_253419144 A-to-I Human chr5 + 139300222 139300222 139300222 TTGTCTCTACTAAAAAATACAGAAAATTTGCCAGGTGTGGTGGTGTGCACCTGTAACCCCAGCTA TTGTCTCTACTAAAAAATACAGAAAATTTGCCTGGTGTGGTGGTGTGCACCTGTAACCCCAGCTA A T MATR3,MATR3:2 Ensembl:ENSG00000280987,Ensembl:ENSG00000015479 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs936880822 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15319055,Human_RBP_ID_22727719 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_118135,RMVar_hsa_circ_234914 51497 RMVar_ID_51497 Human_SNP_ID_253419170 A-to-I Human chr5 + 139300314 139300314 139300314 GGGAACCCGAGAGGCGGAGGTTGCAGTGAGCCAAGATCACGCCATTGCACTCCAGGCCTGGCAAC GGGAACCCGAGAGGCGGAGGTTGCAGTGAGCCCAGATCACGCCATTGCACTCCAGGCCTGGCAAC A C MATR3,MATR3:2 Ensembl:ENSG00000280987,Ensembl:ENSG00000015479 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs983981545 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10184755,Human_RBP_ID_15319059,Human_RBP_ID_22727719,Human_RBP_ID_25937342 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_118135,RMVar_hsa_circ_234914 51498 RMVar_ID_51498 Human_SNP_ID_253419449 A-to-I Human chr5 + 139301334 139301334 139301334 CTTAGGGATACAGAATGGAGCCTTTTTTCTTTATTTGAGACAGAGTCTCACTCTGTCACCCAGGC CTTAGGGATACAGAATGGAGCCTTTTTTCTTTTTTTGAGACAGAGTCTCACTCTGTCACCCAGGC A T MATR3,MATR3:2 Ensembl:ENSG00000280987,Ensembl:ENSG00000015479 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1554145434 Functional Loss SNV dbSNP153 33..33 33 - - - 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_118135,RMVar_hsa_circ_234914 51499 RMVar_ID_51499 Human_SNP_ID_253419478 A-to-I Human chr5 + 139301449 139301449 139301449 TCAAGAGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCGTGTGCCACCACACCCG TCAAGAGATTCTCCTGCCTCAGCCTCCCAAGTGGCTGGGACTACAGGCGTGTGCCACCACACCCG A G MATR3,MATR3:2 Ensembl:ENSG00000280987,Ensembl:ENSG00000015479 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1385506557 Functional Loss SNV dbSNP153 33..33 33 - - - 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_118135,RMVar_hsa_circ_234914 51500 RMVar_ID_51500 Human_SNP_ID_253419980 A-to-I Human chr5 + 139303176 139303176 139303176 CAGGCTGGAGTGCAGTGCCCCAATCTCGGCTCAGTGCAGCCTCCATCTCCCAGGTTCAAGTGATT CAGGCTGGAGTGCAGTGCCCCAATCTCGGCTCGGTGCAGCCTCCATCTCCCAGGTTCAAGTGATT A G MATR3,MATR3:2 Ensembl:ENSG00000280987,Ensembl:ENSG00000015479 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1227409204 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15319211 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_118135,RMVar_hsa_circ_234914 51501 RMVar_ID_51501 Human_SNP_ID_253419996 A-to-I Human chr5 + 139303243 139303243 139303243 CCGGCCTTAGCCTCCCACGTAGGTGGGACTACAGGTGCGTGCCACCATGCCCAGCTAATTTTTAT CCGGCCTTAGCCTCCCACGTAGGTGGGACTACGGGTGCGTGCCACCATGCCCAGCTAATTTTTAT A G MATR3,MATR3:2 Ensembl:ENSG00000280987,Ensembl:ENSG00000015479 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1189175102 Functional Loss SNV dbSNP153 33..33 33 - - - 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_118135,RMVar_hsa_circ_234914 51502 RMVar_ID_51502 Human_SNP_ID_253419997 A-to-I Human chr5 + 139303243 139303243 139303243 CCGGCCTTAGCCTCCCACGTAGGTGGGACTACAGGTGCGTGCCACCATGCCCAGCTAATTTTTAT CCGGCCTTAGCCTCCCACGTAGGTGGGACTACTGGTGCGTGCCACCATGCCCAGCTAATTTTTAT A T MATR3,MATR3:2 Ensembl:ENSG00000280987,Ensembl:ENSG00000015479 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1189175102 Functional Loss SNV dbSNP153 33..33 33 - - - 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_118135,RMVar_hsa_circ_234914 51503 RMVar_ID_51503 Human_SNP_ID_253420087 A-to-I Human chr5 + 139303569 139303569 139303569 AGCCTGGCCAACATGGTGAAAACCCCCTCTCTACCAAAACAATGAAAACTAGCCGAGCATGGTGG AGCCTGGCCAACATGGTGAAAACCCCCTCTCTGCCAAAACAATGAAAACTAGCCGAGCATGGTGG A G MATR3,MATR3:2 Ensembl:ENSG00000280987,Ensembl:ENSG00000015479 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs989191138 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18039951 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_118135,RMVar_hsa_circ_234914 51504 RMVar_ID_51504 Human_SNP_ID_253424913 A-to-I Human chr5 + 139320151 139320151 139320151 TAACACAGTGAAACCCCCTCTCTCCTAAAAATACAAAAAAATTAGCTGGGCGTGGTGGCGTGCGC TAACACAGTGAAACCCCCTCTCTCCTAAAAATTCAAAAAAATTAGCTGGGCGTGGTGGCGTGCGC A T MATR3,MATR3:2 Ensembl:ENSG00000280987,Ensembl:ENSG00000015479 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs937758010 Functional Loss SNV dbSNP153 33..33 33 - - - 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_33277 51505 RMVar_ID_51505 Human_SNP_ID_253425340 A-to-I Human chr5 + 139321355 139321355 139321355 TTGCATTTGTAGTAGAGATGGGGTTTCACCATACTGGTCAGGCTGTTCTCGGAATTCCTGACCTC TTGCATTTGTAGTAGAGATGGGGTTTCACCATGCTGGTCAGGCTGTTCTCGGAATTCCTGACCTC A G MATR3,MATR3:2 Ensembl:ENSG00000280987,Ensembl:ENSG00000015479 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1271593067 Functional Loss SNV dbSNP153 33..33 33 - - - 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_33277 51506 RMVar_ID_51506 Human_SNP_ID_253426150 A-to-I Human chr5 + 139323732 139323731 139323732 CAAGACCAACATGGTGAAACCCCGTCTCTACTAAAAATATGAAAATTAGCCGGGCGTGGTGGCAC CAAGACCAACATGGTGAAACCCCGTCTCTACT_AAAATATGAAAATTAGCCGGGCGTGGTGGCAC TA T MATR3,MATR3:2 Ensembl:ENSG00000280987,Ensembl:ENSG00000015479 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1480571008 Functional Loss DEL dbSNP153 33..33 33 - - - 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 51507 RMVar_ID_51507 Human_SNP_ID_253426187 A-to-I Human chr5 + 139323879 139323879 139323879 CATCACTGTACTCCAGCCTGGGTGACAAGAGCAAGACTGTCTCAAGAAAAAAAAAAAGTAGAGCG CATCACTGTACTCCAGCCTGGGTGACAAGAGCCAGACTGTCTCAAGAAAAAAAAAAAGTAGAGCG A C MATR3,MATR3:2 Ensembl:ENSG00000280987,Ensembl:ENSG00000015479 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs906105016 Functional Loss SNV dbSNP153 33..33 33 - - - 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 51508 RMVar_ID_51508 Human_SNP_ID_253426372 A-to-I Human chr5 + 139324363 139324363 139324363 TTGCCCAGGCTGGAGTGCGGTGGTGTGATCTCAGCTAACTGCAACCTCCACCTCCCAGGTTCAAG TTGCCCAGGCTGGAGTGCGGTGGTGTGATCTCCGCTAACTGCAACCTCCACCTCCCAGGTTCAAG A C MATR3,MATR3:2 Ensembl:ENSG00000280987,Ensembl:ENSG00000015479 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs367952086 Functional Loss SNV dbSNP153 33..33 33 - - - 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 51509 RMVar_ID_51509 Human_SNP_ID_253426403 A-to-I Human chr5 + 139324456 139324456 139324456 GGGATTACAGGTGTCCACCACCACACGAGGCTAATTCTTGTATTTTTAGTAGAAACGAGGTTTCG GGGATTACAGGTGTCCACCACCACACGAGGCTGATTCTTGTATTTTTAGTAGAAACGAGGTTTCG A G MATR3,MATR3:2 Ensembl:ENSG00000280987,Ensembl:ENSG00000015479 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1323927825 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23039754 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 51510 RMVar_ID_51510 Human_SNP_ID_253426407 A-to-I Human chr5 + 139324471 139324471 139324471 CACCACCACACGAGGCTAATTCTTGTATTTTTAGTAGAAACGAGGTTTCGCCATGTTGGCCTGGC CACCACCACACGAGGCTAATTCTTGTATTTTTGGTAGAAACGAGGTTTCGCCATGTTGGCCTGGC A G MATR3,MATR3:2 Ensembl:ENSG00000280987,Ensembl:ENSG00000015479 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs544980221 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17575321,Human_RBP_ID_23039754 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 51511 RMVar_ID_51511 Human_SNP_ID_253426412 A-to-I Human chr5 + 139324481 139324481 139324481 CGAGGCTAATTCTTGTATTTTTAGTAGAAACGAGGTTTCGCCATGTTGGCCTGGCTGGTATTGAA CGAGGCTAATTCTTGTATTTTTAGTAGAAACGCGGTTTCGCCATGTTGGCCTGGCTGGTATTGAA A C MATR3,MATR3:2 Ensembl:ENSG00000280987,Ensembl:ENSG00000015479 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs774333050 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17575321 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 51512 RMVar_ID_51512 Human_SNP_ID_253426418 A-to-I Human chr5 + 139324491 139324491 139324491 TCTTGTATTTTTAGTAGAAACGAGGTTTCGCCATGTTGGCCTGGCTGGTATTGAACTCCTGAGAT TCTTGTATTTTTAGTAGAAACGAGGTTTCGCCGTGTTGGCCTGGCTGGTATTGAACTCCTGAGAT A G MATR3,MATR3:2 Ensembl:ENSG00000280987,Ensembl:ENSG00000015479 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs929847872 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15320297,Human_RBP_ID_17575321,Human_RBP_ID_23313805 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 51513 RMVar_ID_51513 Human_SNP_ID_253426430 A-to-I Human chr5 + 139324555 139324555 139324555 TCTCAGGGTGATCCGCCCACCTCAGCCTCCCAAAGTGCTGGAATTACAGGTGTGAGCCACCATGC TCTCAGGGTGATCCGCCCACCTCAGCCTCCCAGAGTGCTGGAATTACAGGTGTGAGCCACCATGC A G MATR3,MATR3:2 Ensembl:ENSG00000280987,Ensembl:ENSG00000015479 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1355831223 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17575321 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 51514 RMVar_ID_51514 Human_SNP_ID_253427399 A-to-I Human chr5 + 139327521 139327521 139327521 TTGGCTCACCCCAACCCCCGCCTCCCAGGTTCAAGCCATTCTCTTGCCTCAGCCTCCTGAGTATC TTGGCTCACCCCAACCCCCGCCTCCCAGGTTCGAGCCATTCTCTTGCCTCAGCCTCCTGAGTATC A G MATR3,MATR3:2 Ensembl:ENSG00000280987,Ensembl:ENSG00000015479 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1269807621 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85144,RMVar_hsa_circ_234896 51515 RMVar_ID_51515 Human_SNP_ID_253428515 A-to-I Human chr5 + 139330948 139330940 139330948 GAGTAGCTGGGACTACAGGCTCATGCCACTATACCTGGCTAGTTTTTGGTTTTTTTGTATAGATG GAGTAGCTGGGACTACAGGCTCATG________CCTGGCTAGTTTTTGGTTTTTTTGTATAGATG GCCACTATA G MATR3,MATR3:2 Ensembl:ENSG00000280987,Ensembl:ENSG00000015479 Protein coding,Protein coding 3'UTR,3'UTR GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1309658840 Functional Loss DEL dbSNP153 26..33 33 - - - Human_RBP_ID_2899957,Human_RBP_ID_7392401,Human_RBP_ID_18833875 Human_miRNA_ID_1632794,Human_miRNA_ID_1632795,Human_miRNA_ID_1673292,Human_miRNA_ID_1673293 RMVar_hsa_circ_85144,RMVar_hsa_circ_234896,RMVar_hsa_circ_234924 51516 RMVar_ID_51516 Human_SNP_ID_253428518 A-to-I Human chr5 + 139330948 139330948 139330948 GAGTAGCTGGGACTACAGGCTCATGCCACTATACCTGGCTAGTTTTTGGTTTTTTTGTATAGATG GAGTAGCTGGGACTACAGGCTCATGCCACTATGCCTGGCTAGTTTTTGGTTTTTTTGTATAGATG A G MATR3,MATR3:2 Ensembl:ENSG00000280987,Ensembl:ENSG00000015479 Protein coding,Protein coding 3'UTR,3'UTR GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1214279444 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2899957,Human_RBP_ID_7392401,Human_RBP_ID_18833875 Human_miRNA_ID_1632794,Human_miRNA_ID_1632795,Human_miRNA_ID_1673292,Human_miRNA_ID_1673293 RMVar_hsa_circ_85144,RMVar_hsa_circ_234896,RMVar_hsa_circ_234924 51517 RMVar_ID_51517 Human_SNP_ID_253428519 A-to-I Human chr5 + 139330948 139330948 139330948 GAGTAGCTGGGACTACAGGCTCATGCCACTATACCTGGCTAGTTTTTGGTTTTTTTGTATAGATG GAGTAGCTGGGACTACAGGCTCATGCCACTATTCCTGGCTAGTTTTTGGTTTTTTTGTATAGATG A T MATR3,MATR3:2 Ensembl:ENSG00000280987,Ensembl:ENSG00000015479 Protein coding,Protein coding 3'UTR,3'UTR GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1214279444 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_2899957,Human_RBP_ID_7392401,Human_RBP_ID_18833875 Human_miRNA_ID_1632794,Human_miRNA_ID_1632795,Human_miRNA_ID_1673292,Human_miRNA_ID_1673293 RMVar_hsa_circ_85144,RMVar_hsa_circ_234896,RMVar_hsa_circ_234924 51518 RMVar_ID_51518 Human_SNP_ID_253429883 A-to-I Human chr5 + 139334882 139334882 139334882 GTCTTTACTAAAAATACAAAAATTAGTCGGGCATGGTGGTAGGGGACTGTAATCCCAGCTACTTA GTCTTTACTAAAAATACAAAAATTAGTCGGGCGTGGTGGTAGGGGACTGTAATCCCAGCTACTTA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1032518110 Functional Loss SNV dbSNP153 33..33 33 - - - 51519 RMVar_ID_51519 Human_SNP_ID_253433756 A-to-I Human chr5 + 139348424 139348424 139348424 TCGCCCAAGTTGGAGTGCAGTGGCGTAGTCTCAGCTGACTGCAAGCTCTGCCTCCCGGGTTCACG TCGCCCAAGTTGGAGTGCAGTGGCGTAGTCTCGGCTGACTGCAAGCTCTGCCTCCCGGGTTCACG A G PAIP2 Ensembl:ENSG00000120727 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1350030548 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7392562,Human_RBP_ID_15321162 51520 RMVar_ID_51520 Human_SNP_ID_253434979 A-to-I Human chr5 + 139352861 139352861 139352861 AGATGAGGCTGGGTGCGTTGGCTCACGCCTGTAATCCAGCACTTTGGGAGGCCAAAGTGGGCAGA AGATGAGGCTGGGTGCGTTGGCTCACGCCTGTTATCCAGCACTTTGGGAGGCCAAAGTGGGCAGA A T PAIP2 Ensembl:ENSG00000120727 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1347177279 Functional Loss SNV dbSNP153 33..33 33 - - - 51521 RMVar_ID_51521 Human_SNP_ID_253447583 A-to-I Human chr5 + 139398436 139398436 139398436 TAAAAAAAAAAAAAACAAAAAACTAGCTGGGCATGGTGTTGGAACATGCCTATAGTCCTGGCTAC TAAAAAAAAAAAAAACAAAAAACTAGCTGGGCGTGGTGTTGGAACATGCCTATAGTCCTGGCTAC A G - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs890519836 Functional Loss SNV dbSNP153 33..33 33 - - - 51522 RMVar_ID_51522 Human_SNP_ID_253447635 A-to-I Human chr5 - 139398701 139398701 139398701 AACCTTTGAAGACAGTAGGATTTTCTTTCTGTAGGAATCAGAATTTTCCAAGGTGCCATGTGGGG AACCTTTGAAGACAGTAGGATTTTCTTTCTGTGGGAATCAGAATTTTCCAAGGTGCCATGTGGGG T C SPATA24 Ensembl:ENSG00000170469 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1561992232 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15321819,Human_RBP_ID_18353997 51523 RMVar_ID_51523 Human_SNP_ID_253447763 A-to-I Human chr5 + 139399170 139399170 139399170 AAACCTTGTCTCTACTAAAAATACAAAAAATTAGCCAGGTGTGGTGGCGGGCACCTATAGTCCCA AAACCTTGTCTCTACTAAAAATACAAAAAATTTGCCAGGTGTGGTGGCGGGCACCTATAGTCCCA A T RF00017-4508 RNACentral:URS000093D619 SRP RNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1334408522 Functional Loss SNV dbSNP153 33..33 33 - - - 51524 RMVar_ID_51524 Human_SNP_ID_253447772 A-to-I Human chr5 + 139399194 139399194 139399194 AAAAAATTAGCCAGGTGTGGTGGCGGGCACCTATAGTCCCAGCTACCTGGGAGGCTGAGGCAGGA AAAAAATTAGCCAGGTGTGGTGGCGGGCACCTGTAGTCCCAGCTACCTGGGAGGCTGAGGCAGGA A G RF00017-4508 RNACentral:URS000093D619 SRP RNA intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1307711930 Functional Loss SNV dbSNP153 33..33 33 - - - 51525 RMVar_ID_51525 Human_SNP_ID_253450899 A-to-I Human chr5 - 139413102 139413102 139413102 ATTGAGTGCCTACTATAAAAGCAGGGGCTCTCACACATATTTTCTTACTTAAACCTCCTCACAAC ATTGAGTGCCTACTATAAAAGCAGGGGCTCTCGCACATATTTTCTTACTTAAACCTCCTCACAAC T C DNAJC18 Ensembl:ENSG00000170464 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs1001741265 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17298317,Human_RBP_ID_17527683 51526 RMVar_ID_51526 Human_SNP_ID_253488818 A-to-I Human chr5 + 139563820 139563820 139563820 AGCCGGGCTTGGTGGCGGGTTCCTGTAGTCCCAGCTACTCTGGAGGCTGAGGCAGGAGAATGACG AGCCGGGCTTGGTGGCGGGTTCCTGTAGTCCCTGCTACTCTGGAGGCTGAGGCAGGAGAATGACG A T UBE2D2 Ensembl:ENSG00000131508 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs969593603 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95625,RMVar_hsa_circ_234944 51527 RMVar_ID_51527 Human_SNP_ID_253488819 A-to-I Human chr5 + 139563824 139563824 139563824 GGGCTTGGTGGCGGGTTCCTGTAGTCCCAGCTACTCTGGAGGCTGAGGCAGGAGAATGACGTGAA GGGCTTGGTGGCGGGTTCCTGTAGTCCCAGCTGCTCTGGAGGCTGAGGCAGGAGAATGACGTGAA A G UBE2D2 Ensembl:ENSG00000131508 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982055779 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95625,RMVar_hsa_circ_234944 51528 RMVar_ID_51528 Human_SNP_ID_253488931 A-to-I Human chr5 + 139564215 139564215 139564215 CAGTCTTGTCGCCCAGGCTGGAATGCAATGGCACGATCTCAGCTCACCGCAACCTCCACCTCCTG CAGTCTTGTCGCCCAGGCTGGAATGCAATGGCTCGATCTCAGCTCACCGCAACCTCCACCTCCTG A T UBE2D2 Ensembl:ENSG00000131508 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1295035051 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95625,RMVar_hsa_circ_234944 51529 RMVar_ID_51529 Human_SNP_ID_253489393 A-to-I Human chr5 + 139566193 139566193 139566193 GGCACTCACCACCATGCCCAGCTAATTTTTGTATTTTTAATAGAGACAGGGTTTCTCCCTGTTGG GGCACTCACCACCATGCCCAGCTAATTTTTGTGTTTTTAATAGAGACAGGGTTTCTCCCTGTTGG A G UBE2D2 Ensembl:ENSG00000131508 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1429173727 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95625,RMVar_hsa_circ_234944 51530 RMVar_ID_51530 Human_SNP_ID_253489468 A-to-I Human chr5 + 139566418 139566418 139566418 ACAGTGGGTCATGCACAGTGGGTCACGCCTGTAATCCCAGCACTTTGGGAGGCCCAGGTGGGCAG ACAGTGGGTCATGCACAGTGGGTCACGCCTGTTATCCCAGCACTTTGGGAGGCCCAGGTGGGCAG A T UBE2D2 Ensembl:ENSG00000131508 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1414832150 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95625,RMVar_hsa_circ_234944 51531 RMVar_ID_51531 Human_SNP_ID_253489506 A-to-I Human chr5 + 139566554 139566554 139566554 AAAATTAGCTGGGTATGGTGGTGGATGGCTGTAGTCCCAGCTAGGTGGGAGGCTGAGGTGGGAGG AAAATTAGCTGGGTATGGTGGTGGATGGCTGTGGTCCCAGCTAGGTGGGAGGCTGAGGTGGGAGG A G UBE2D2 Ensembl:ENSG00000131508 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs560463354 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17575536 RMVar_hsa_circ_95625,RMVar_hsa_circ_234944 51532 RMVar_ID_51532 Human_SNP_ID_253490175 A-to-I Human chr5 + 139568872 139568872 139568872 GAGCACCTGTGATCCCAGTTACTGGGGAGGCTAAGGCAGAGAGTTGCTTGAACCCGGGAGGTGGA GAGCACCTGTGATCCCAGTTACTGGGGAGGCTGAGGCAGAGAGTTGCTTGAACCCGGGAGGTGGA A G UBE2D2 Ensembl:ENSG00000131508 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs757420632 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23313810 RMVar_hsa_circ_95625,RMVar_hsa_circ_234944 51533 RMVar_ID_51533 Human_SNP_ID_253491937 A-to-I Human chr5 + 139575768 139575768 139575768 TTGAAATTAGCTGGGTACAGTGGCTCATGCCTATAATCTCAGTGCTTTGGGAGGCCAAGGTGGGA TTGAAATTAGCTGGGTACAGTGGCTCATGCCTGTAATCTCAGTGCTTTGGGAGGCCAAGGTGGGA A G UBE2D2 Ensembl:ENSG00000131508 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1289032030 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95625,RMVar_hsa_circ_234944 51534 RMVar_ID_51534 Human_SNP_ID_253491963 A-to-I Human chr5 + 139575907 139575907 139575907 AGGTTTGGTGGCACACGCCTGTAGTCATAGCTACTGGGAAGACTGAGGTGGAAGAGGAGGATCTC AGGTTTGGTGGCACACGCCTGTAGTCATAGCTGCTGGGAAGACTGAGGTGGAAGAGGAGGATCTC A G UBE2D2 Ensembl:ENSG00000131508 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs767102687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17575541 RMVar_hsa_circ_95625,RMVar_hsa_circ_234944 51535 RMVar_ID_51535 Human_SNP_ID_253491964 A-to-I Human chr5 + 139575907 139575907 139575907 AGGTTTGGTGGCACACGCCTGTAGTCATAGCTACTGGGAAGACTGAGGTGGAAGAGGAGGATCTC AGGTTTGGTGGCACACGCCTGTAGTCATAGCTTCTGGGAAGACTGAGGTGGAAGAGGAGGATCTC A T UBE2D2 Ensembl:ENSG00000131508 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs767102687 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17575541 RMVar_hsa_circ_95625,RMVar_hsa_circ_234944 51536 RMVar_ID_51536 Human_SNP_ID_253492106 A-to-I Human chr5 + 139576508 139576508 139576508 CCCAAAGATGATTTTTTTTTTTGAGACGGACTACAGACACGTGCCACCACGCCCGGCAAATTTTT CCCAAAGATGATTTTTTTTTTTGAGACGGACTGCAGACACGTGCCACCACGCCCGGCAAATTTTT A G UBE2D2 Ensembl:ENSG00000131508 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs571719709 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7392989,Human_RBP_ID_10185437,Human_RBP_ID_15322316,Human_RBP_ID_24086126 RMVar_hsa_circ_95625,RMVar_hsa_circ_234944 51537 RMVar_ID_51537 Human_SNP_ID_253492424 A-to-I Human chr5 + 139577561 139577561 139577561 ACATCCTCTCGAGTAGCTAGGATTACAGGTGCATGCCACCACGTCTGGCTAATTATTGTATTTTT ACATCCTCTCGAGTAGCTAGGATTACAGGTGCTTGCCACCACGTCTGGCTAATTATTGTATTTTT A T UBE2D2 Ensembl:ENSG00000131508 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs762305761 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95625,RMVar_hsa_circ_234944 51538 RMVar_ID_51538 Human_SNP_ID_253492698 A-to-I Human chr5 + 139578636 139578636 139578636 TACCATACCTGGCTTTTTAAAAAAATTTTTGTAGAGATAGGGTCTTGCTGTGTGGCCCAGGCTGC TACCATACCTGGCTTTTTAAAAAAATTTTTGTGGAGATAGGGTCTTGCTGTGTGGCCCAGGCTGC A G UBE2D2 Ensembl:ENSG00000131508 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs977718927 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7392999 RMVar_hsa_circ_95625,RMVar_hsa_circ_234944 51539 RMVar_ID_51539 Human_SNP_ID_253492906 A-to-I Human chr5 + 139579551 139579551 139579551 CCTCAAGATGATCCGCCCACCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAACAACTGTGT CCTCAAGATGATCCGCCCACCTTGGCCTCCCAGAGTGCTGGGATTACAGGCATGAACAACTGTGT A G UBE2D2 Ensembl:ENSG00000131508 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1336341165 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25862751 RMVar_hsa_circ_95625,RMVar_hsa_circ_234944 51540 RMVar_ID_51540 Human_SNP_ID_253493567 A-to-I Human chr5 + 139582009 139582009 139582009 GTTTTTTTTTGTTTTTGTTTTTTTTTGAAGATAGAGTCTCACTTTGTTGCCCAGGCTGGAGTGCG GTTTTTTTTTGTTTTTGTTTTTTTTTGAAGATGGAGTCTCACTTTGTTGCCCAGGCTGGAGTGCG A G UBE2D2 Ensembl:ENSG00000131508 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs546905913 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3759626,Human_RBP_ID_23192193 RMVar_hsa_circ_95625,RMVar_hsa_circ_234944 51541 RMVar_ID_51541 Human_SNP_ID_253493979 A-to-I Human chr5 + 139583484 139583484 139583484 TATACAATTTTGTCAATTTAAAGAAGTTGGCCAGGTGCAGTGGCTTACGCCTGTAATCCCAGAAC TATACAATTTTGTCAATTTAAAGAAGTTGGCCGGGTGCAGTGGCTTACGCCTGTAATCCCAGAAC A G UBE2D2 Ensembl:ENSG00000131508 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1488859138 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95625,RMVar_hsa_circ_234944 51542 RMVar_ID_51542 Human_SNP_ID_253493990 A-to-I Human chr5 + 139583506 139583505 139583506 GAAGTTGGCCAGGTGCAGTGGCTTACGCCTGTAATCCCAGAACTTTGGGAGGCTGAGGTGGGTGG GAAGTTGGCCAGGTGCAGTGGCTTACGCCTGT_ATCCCAGAACTTTGGGAGGCTGAGGTGGGTGG TA T UBE2D2 Ensembl:ENSG00000131508 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1177127691 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_95625,RMVar_hsa_circ_234944 51543 RMVar_ID_51543 Human_SNP_ID_253494415 A-to-I Human chr5 + 139585008 139585008 139585008 CTGCAACCTCCATCTCTTGGGTTCAAGTGATTATCTTGCCTCAGCCTCCCATGTAGCTGGGATTA CTGCAACCTCCATCTCTTGGGTTCAAGTGATTGTCTTGCCTCAGCCTCCCATGTAGCTGGGATTA A G UBE2D2 Ensembl:ENSG00000131508 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1302868532 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95625,RMVar_hsa_circ_234944 51544 RMVar_ID_51544 Human_SNP_ID_253495319 A-to-I Human chr5 + 139588139 139588139 139588139 ATGTGTGCCACCATGCCTGGCTAAATGTTTCTATTTTGTAGAGATGGAGTCTTGCTGTGTTGCCT ATGTGTGCCACCATGCCTGGCTAAATGTTTCTGTTTTGTAGAGATGGAGTCTTGCTGTGTTGCCT A G UBE2D2 Ensembl:ENSG00000131508 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs945700760 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7393021 RMVar_hsa_circ_95625,RMVar_hsa_circ_234944 51545 RMVar_ID_51545 Human_SNP_ID_253495491 A-to-I Human chr5 + 139588790 139588790 139588790 CTGGAACCTGATGTAACTTCTTTTGTTTTTTGAGATAGGGTCTTGCCCTGTCACCCAGGGTGAAG CTGGAACCTGATGTAACTTCTTTTGTTTTTTGTGATAGGGTCTTGCCCTGTCACCCAGGGTGAAG A T UBE2D2 Ensembl:ENSG00000131508 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1257948000 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95625,RMVar_hsa_circ_234944 51546 RMVar_ID_51546 Human_SNP_ID_253495501 A-to-I Human chr5 + 139588842 139588842 139588842 ACCCAGGGTGAAGTGCAGTGGCTACTCATTGCAGCCTCGACCTCCTGGGCTCAAGTGATCCTCCC ACCCAGGGTGAAGTGCAGTGGCTACTCATTGCGGCCTCGACCTCCTGGGCTCAAGTGATCCTCCC A G UBE2D2 Ensembl:ENSG00000131508 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1358971412 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95625,RMVar_hsa_circ_234944 51547 RMVar_ID_51547 Human_SNP_ID_253495536 A-to-I Human chr5 + 139588994 139588994 139588994 TTTTAAATGTTTTGTAGAGACAAGGTCTCCCTATGTTGCCCAGGCTGGTCTCAAACTCCTGGGCT TTTTAAATGTTTTGTAGAGACAAGGTCTCCCTGTGTTGCCCAGGCTGGTCTCAAACTCCTGGGCT A G UBE2D2 Ensembl:ENSG00000131508 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs771824397 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95625,RMVar_hsa_circ_234944 51548 RMVar_ID_51548 Human_SNP_ID_253496895 A-to-I Human chr5 + 139593724 139593724 139593724 GCCTTGAACTCCTGGGCTCAAGCAATCCTCCTACCTCAGCCTCCCAGGTAGCTAGGACTACAGGC GCCTTGAACTCCTGGGCTCAAGCAATCCTCCTCCCTCAGCCTCCCAGGTAGCTAGGACTACAGGC A C UBE2D2 Ensembl:ENSG00000131508 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1426573232 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95625,RMVar_hsa_circ_234944 51549 RMVar_ID_51549 Human_SNP_ID_253496896 A-to-I Human chr5 + 139593724 139593724 139593724 GCCTTGAACTCCTGGGCTCAAGCAATCCTCCTACCTCAGCCTCCCAGGTAGCTAGGACTACAGGC GCCTTGAACTCCTGGGCTCAAGCAATCCTCCTGCCTCAGCCTCCCAGGTAGCTAGGACTACAGGC A G UBE2D2 Ensembl:ENSG00000131508 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1426573232 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95625,RMVar_hsa_circ_234944 51550 RMVar_ID_51550 Human_SNP_ID_253498483 A-to-I Human chr5 + 139599933 139599933 139599933 TCAAGGGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGTATGACAGGCATGTATCACCATGCCCA TCAAGGGATTCTCCTGCCTCAGCCTCCTGAGTGGCTGGTATGACAGGCATGTATCACCATGCCCA A G UBE2D2 Ensembl:ENSG00000131508 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1033994476 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95625,RMVar_hsa_circ_234944 51551 RMVar_ID_51551 Human_SNP_ID_253498730 A-to-I Human chr5 + 139600986 139600986 139600986 CACCACGCCTGATTAATTTTTGTATTTTTAGTAGATTCGTGGTTTCGCCATGTTGGCCAGGCTGG CACCACGCCTGATTAATTTTTGTATTTTTAGTGGATTCGTGGTTTCGCCATGTTGGCCAGGCTGG A G UBE2D2 Ensembl:ENSG00000131508 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1393435447 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15322861 RMVar_hsa_circ_95625,RMVar_hsa_circ_234945,RMVar_hsa_circ_285724,RMVar_hsa_circ_297177,RMVar_hsa_circ_234944,RMVar_hsa_circ_289943,RMVar_hsa_circ_234946 51552 RMVar_ID_51552 Human_SNP_ID_253499059 A-to-I Human chr5 + 139602217 139602217 139602217 TGGATTACAGGCACCTGCCACCACACCTGGCTAGTTTTTGTATTTTTAGTAGAGACGGGGTTTCG TGGATTACAGGCACCTGCCACCACACCTGGCTGGTTTTTGTATTTTTAGTAGAGACGGGGTTTCG A G UBE2D2 Ensembl:ENSG00000131508 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1479550942 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95625,RMVar_hsa_circ_234945,RMVar_hsa_circ_285724,RMVar_hsa_circ_297177,RMVar_hsa_circ_234944,RMVar_hsa_circ_289943,RMVar_hsa_circ_234946 51553 RMVar_ID_51553 Human_SNP_ID_253499148 A-to-I Human chr5 + 139602579 139602579 139602579 GCATGCCTGTAGCCCCAGCTACTCAGGAGTTTAAGGTGGGAGGATCGCTTGAGTCCAGGCAGTTG GCATGCCTGTAGCCCCAGCTACTCAGGAGTTTGAGGTGGGAGGATCGCTTGAGTCCAGGCAGTTG A G UBE2D2 Ensembl:ENSG00000131508 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs114312400 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3759646 RMVar_hsa_circ_95625,RMVar_hsa_circ_234945,RMVar_hsa_circ_285724,RMVar_hsa_circ_297177,RMVar_hsa_circ_234944,RMVar_hsa_circ_289943,RMVar_hsa_circ_234946 51554 RMVar_ID_51554 Human_SNP_ID_253500134 A-to-I Human chr5 + 139606346 139606346 139606346 ACCACGACCGACTAATTTTTTGTATTTTTAGTAGAGACTGGGTTTCACCATGTTGGCCAGGCTGG ACCACGACCGACTAATTTTTTGTATTTTTAGTGGAGACTGGGTTTCACCATGTTGGCCAGGCTGG A G UBE2D2 Ensembl:ENSG00000131508 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs924768149 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95625,RMVar_hsa_circ_234945,RMVar_hsa_circ_285724,RMVar_hsa_circ_297177,RMVar_hsa_circ_234944,RMVar_hsa_circ_289943,RMVar_hsa_circ_234946 51555 RMVar_ID_51555 Human_SNP_ID_253500255 A-to-I Human chr5 + 139606866 139606866 139606866 CTCACATCGTCGCCCCCCTGGAGTGTAGTGGCATGATCTTGGCTCACTGCAACCTCTGCCTCCCG CTCACATCGTCGCCCCCCTGGAGTGTAGTGGCGTGATCTTGGCTCACTGCAACCTCTGCCTCCCG A G UBE2D2 Ensembl:ENSG00000131508 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1371823822 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15322950 RMVar_hsa_circ_95625,RMVar_hsa_circ_234945,RMVar_hsa_circ_285724,RMVar_hsa_circ_297177,RMVar_hsa_circ_234944,RMVar_hsa_circ_289943,RMVar_hsa_circ_234946 51556 RMVar_ID_51556 Human_SNP_ID_253500291 A-to-I Human chr5 + 139606989 139606989 139606989 ACCACGCCCAGCTAATTTTTTGTATTTTTAGTAGAGACGGTATTTCACCATGTTGGCCAGGCTGG ACCACGCCCAGCTAATTTTTTGTATTTTTAGTGGAGACGGTATTTCACCATGTTGGCCAGGCTGG A G UBE2D2 Ensembl:ENSG00000131508 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs998800295 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95625,RMVar_hsa_circ_234945,RMVar_hsa_circ_285724,RMVar_hsa_circ_297177,RMVar_hsa_circ_234944,RMVar_hsa_circ_289943,RMVar_hsa_circ_234946 51557 RMVar_ID_51557 Human_SNP_ID_253500773 A-to-I Human chr5 + 139608956 139608956 139608956 AAAATACAGCAAAATTAGTCAGGTGTGGTGGCACACACCTGTAATCCCAGCTACTCAGGGAGCTG AAAATACAGCAAAATTAGTCAGGTGTGGTGGCCCACACCTGTAATCCCAGCTACTCAGGGAGCTG A C UBE2D2 Ensembl:ENSG00000131508 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs12513420 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95625,RMVar_hsa_circ_234945,RMVar_hsa_circ_285724,RMVar_hsa_circ_297177,RMVar_hsa_circ_234944,RMVar_hsa_circ_289943,RMVar_hsa_circ_234946 51558 RMVar_ID_51558 Human_SNP_ID_253500774 A-to-I Human chr5 + 139608956 139608956 139608956 AAAATACAGCAAAATTAGTCAGGTGTGGTGGCACACACCTGTAATCCCAGCTACTCAGGGAGCTG AAAATACAGCAAAATTAGTCAGGTGTGGTGGCTCACACCTGTAATCCCAGCTACTCAGGGAGCTG A T UBE2D2 Ensembl:ENSG00000131508 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs12513420 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95625,RMVar_hsa_circ_234945,RMVar_hsa_circ_285724,RMVar_hsa_circ_297177,RMVar_hsa_circ_234944,RMVar_hsa_circ_289943,RMVar_hsa_circ_234946 51559 RMVar_ID_51559 Human_SNP_ID_253500894 A-to-I Human chr5 + 139609510 139609510 139609510 CTTCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCAATGCGCCACCATGCTTGGCTAATTTT CTTCTGCCTCAGCCTCCCGAGTAGCTGGGATTGCAGGCAATGCGCCACCATGCTTGGCTAATTTT A G UBE2D2 Ensembl:ENSG00000131508 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs960152228 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95625,RMVar_hsa_circ_234945,RMVar_hsa_circ_285724,RMVar_hsa_circ_297177,RMVar_hsa_circ_234944,RMVar_hsa_circ_289943,RMVar_hsa_circ_234946 51560 RMVar_ID_51560 Human_SNP_ID_253501450 A-to-I Human chr5 + 139611352 139611352 139611352 GGGATTACAGACGCCCGCCATCACGCCCAGCTAATTTTTTATATTTTCAGTAGAGACGGGGTTTC GGGATTACAGACGCCCGCCATCACGCCCAGCTGATTTTTTATATTTTCAGTAGAGACGGGGTTTC A G UBE2D2 Ensembl:ENSG00000131508 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1013265156 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15323015 RMVar_hsa_circ_95625,RMVar_hsa_circ_234945,RMVar_hsa_circ_285724,RMVar_hsa_circ_297177,RMVar_hsa_circ_234944,RMVar_hsa_circ_289943,RMVar_hsa_circ_234946 51561 RMVar_ID_51561 Human_SNP_ID_253501451 A-to-I Human chr5 + 139611362 139611362 139611362 ACGCCCGCCATCACGCCCAGCTAATTTTTTATATTTTCAGTAGAGACGGGGTTTCACTATGTTGG ACGCCCGCCATCACGCCCAGCTAATTTTTTATGTTTTCAGTAGAGACGGGGTTTCACTATGTTGG A G UBE2D2 Ensembl:ENSG00000131508 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1171372389 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15323015 RMVar_hsa_circ_95625,RMVar_hsa_circ_234945,RMVar_hsa_circ_285724,RMVar_hsa_circ_297177,RMVar_hsa_circ_234944,RMVar_hsa_circ_289943,RMVar_hsa_circ_234946 51562 RMVar_ID_51562 Human_SNP_ID_253501459 A-to-I Human chr5 + 139611388 139611388 139611388 TTTTATATTTTCAGTAGAGACGGGGTTTCACTATGTTGGTCAGGCTGATCTCGAACTCCTGACCT TTTTATATTTTCAGTAGAGACGGGGTTTCACTGTGTTGGTCAGGCTGATCTCGAACTCCTGACCT A G UBE2D2 Ensembl:ENSG00000131508 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1301002037 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95625,RMVar_hsa_circ_234945,RMVar_hsa_circ_285724,RMVar_hsa_circ_297177,RMVar_hsa_circ_234944,RMVar_hsa_circ_289943,RMVar_hsa_circ_234946 51563 RMVar_ID_51563 Human_SNP_ID_253501460 A-to-I Human chr5 + 139611388 139611388 139611388 TTTTATATTTTCAGTAGAGACGGGGTTTCACTATGTTGGTCAGGCTGATCTCGAACTCCTGACCT TTTTATATTTTCAGTAGAGACGGGGTTTCACTTTGTTGGTCAGGCTGATCTCGAACTCCTGACCT A T UBE2D2 Ensembl:ENSG00000131508 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1301002037 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95625,RMVar_hsa_circ_234945,RMVar_hsa_circ_285724,RMVar_hsa_circ_297177,RMVar_hsa_circ_234944,RMVar_hsa_circ_289943,RMVar_hsa_circ_234946 51564 RMVar_ID_51564 Human_SNP_ID_253502809 A-to-I Human chr5 + 139617072 139617072 139617072 AGGTGTGATGGTGCGTGCCTGTAGTCCCAACTACTCAGGAGGCTGAGGCGGGAGAATCACTTGAA AGGTGTGATGGTGCGTGCCTGTAGTCCCAACTGCTCAGGAGGCTGAGGCGGGAGAATCACTTGAA A G UBE2D2 Ensembl:ENSG00000131508 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs946071957 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11514,RMVar_hsa_circ_297177,RMVar_hsa_circ_289943,RMVar_hsa_circ_234946,RMVar_hsa_circ_288920,RMVar_hsa_circ_366211,RMVar_hsa_circ_105030,RMVar_hsa_circ_234948,RMVar_hsa_circ_285172,RMVar_hsa_circ_234947,RMVar_hsa_circ_234952 51565 RMVar_ID_51565 Human_SNP_ID_253503655 A-to-I Human chr5 + 139620976 139620976 139620976 ATAAGTTAATGATAGATATGGCCGGGTGTGGTAGTTCACGCCTGTAATCCCAGCACTTCGGGAGG ATAAGTTAATGATAGATATGGCCGGGTGTGGTTGTTCACGCCTGTAATCCCAGCACTTCGGGAGG A T UBE2D2 Ensembl:ENSG00000131508 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1422022350 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11514,RMVar_hsa_circ_297177,RMVar_hsa_circ_289943,RMVar_hsa_circ_234946,RMVar_hsa_circ_288920,RMVar_hsa_circ_366211,RMVar_hsa_circ_105030,RMVar_hsa_circ_234948,RMVar_hsa_circ_285172,RMVar_hsa_circ_234947,RMVar_hsa_circ_234952 51566 RMVar_ID_51566 Human_SNP_ID_253504549 A-to-I Human chr5 + 139624659 139624659 139624659 AATACAAAAATTAGCCGGGCATGGTGGCGGGCACCTGTAATCGCAGCTACTCGAGAGGCTGAGAT AATACAAAAATTAGCCGGGCATGGTGGCGGGCGCCTGTAATCGCAGCTACTCGAGAGGCTGAGAT A G UBE2D2 Ensembl:ENSG00000131508 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1194820052 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11514,RMVar_hsa_circ_297177,RMVar_hsa_circ_366211,RMVar_hsa_circ_105030,RMVar_hsa_circ_234947,RMVar_hsa_circ_118682,RMVar_hsa_circ_298076,RMVar_hsa_circ_234954 51567 RMVar_ID_51567 Human_SNP_ID_253505007 A-to-I Human chr5 + 139626214 139626214 139626214 CCTCAGCCTCCTGAGTAGCTGGGACTATAGTCATGCGCCACCACACCCTGCTAATTTTTGTATTT CCTCAGCCTCCTGAGTAGCTGGGACTATAGTCGTGCGCCACCACACCCTGCTAATTTTTGTATTT A G UBE2D2 Ensembl:ENSG00000131508 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984160565 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15323440 RMVar_hsa_circ_11514,RMVar_hsa_circ_297177,RMVar_hsa_circ_366211,RMVar_hsa_circ_105030,RMVar_hsa_circ_234947,RMVar_hsa_circ_118682,RMVar_hsa_circ_298076,RMVar_hsa_circ_234954 51568 RMVar_ID_51568 Human_SNP_ID_253668019 A-to-I Human chr5 - 140339478 140339478 140339478 TGAGGCAGGAGAATCTCTCAAACCCAGGAGGCAGAACTTGCAGTGAGCCGAGATAGTGCCATTGC TGAGGCAGGAGAATCTCTCAAACCCAGGAGGCGGAACTTGCAGTGAGCCGAGATAGTGCCATTGC T C HBEGF Ensembl:ENSG00000113070 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs567835148 Functional Loss SNV dbSNP153 33..33 33 - - - 51569 RMVar_ID_51569 Human_SNP_ID_253668205 A-to-I Human chr5 - 140340239 140340239 140340239 CTCTGTCACCCAGGCTGGAGTGCAGTGACACAATCTCGGCTCTCTGCAGCCTCCGCCTCCCAGAT CTCTGTCACCCAGGCTGGAGTGCAGTGACACAGTCTCGGCTCTCTGCAGCCTCCGCCTCCCAGAT T C HBEGF Ensembl:ENSG00000113070 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs866821308 Functional Loss SNV dbSNP153 33..33 33 - - - 51570 RMVar_ID_51570 Human_SNP_ID_253683863 A-to-I Human chr5 + 140404562 140404562 140404562 TCAAGCTATTTTCCTGCCTCAGCCTCCCTAGTAACTGGGATTCCAGGTGCCTGCTACCACGACTG TCAAGCTATTTTCCTGCCTCAGCCTCCCTAGTGACTGGGATTCCAGGTGCCTGCTACCACGACTG A G ANKHD1-EIF4EBP3,ANKHD1 Ensembl:ENSG00000254996,Ensembl:ENSG00000131503 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1023480721 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120852,RMVar_hsa_circ_234972 51571 RMVar_ID_51571 Human_SNP_ID_253684235 A-to-I Human chr5 + 140406056 140406056 140406056 GAGGTCAGGAGTTAGAGACCAGCCTGGCCAACATGGCAAAATTCTGTCTCTATTAAAACAAAAAA GAGGTCAGGAGTTAGAGACCAGCCTGGCCAACGTGGCAAAATTCTGTCTCTATTAAAACAAAAAA A G ANKHD1-EIF4EBP3,ANKHD1 Ensembl:ENSG00000254996,Ensembl:ENSG00000131503 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1023391433 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120852,RMVar_hsa_circ_234972 51572 RMVar_ID_51572 Human_SNP_ID_253686106 A-to-I Human chr5 + 140413981 140413981 140413981 TTTTGTATTTTTAGTGGAGATGGGGTTTTGCTATGTAGGCCAGGCTTGTCTCAAACTCCTGACCT TTTTGTATTTTTAGTGGAGATGGGGTTTTGCTGTGTAGGCCAGGCTTGTCTCAAACTCCTGACCT A G ANKHD1-EIF4EBP3,ANKHD1 Ensembl:ENSG00000254996,Ensembl:ENSG00000131503 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs972012276 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15325881 RMVar_hsa_circ_120852,RMVar_hsa_circ_234972 51573 RMVar_ID_51573 Human_SNP_ID_253686261 A-to-I Human chr5 + 140414712 140414712 140414712 AAAATTAGCCAGGCATGGTGGCACATGCCTGTAGTCCCAGCTACTCAAGAGGCTGAGGTGGGAGG AAAATTAGCCAGGCATGGTGGCACATGCCTGTGGTCCCAGCTACTCAAGAGGCTGAGGTGGGAGG A G ANKHD1-EIF4EBP3,ANKHD1 Ensembl:ENSG00000254996,Ensembl:ENSG00000131503 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1349320738 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120852,RMVar_hsa_circ_234972 51574 RMVar_ID_51574 Human_SNP_ID_253686502 A-to-I Human chr5 + 140415556 140415556 140415556 CACCTTCTGGGTTCAGGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGTGCACG CACCTTCTGGGTTCAGGCGATTCTCCTGCCTCGGCCTCCCAAGTAGCTGGGATTACAGGTGCACG A G ANKHD1-EIF4EBP3,ANKHD1 Ensembl:ENSG00000254996,Ensembl:ENSG00000131503 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1404198401 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120852,RMVar_hsa_circ_234972 51575 RMVar_ID_51575 Human_SNP_ID_253694217 A-to-I Human chr5 + 140445032 140445032 140445032 GTATGCCACCATTCCTGGCTCAGTTTTTTTTTAGTAGAGATACTGTGTTGTTCAGGCTGGTCTCA GTATGCCACCATTCCTGGCTCAGTTTTTTTTTGGTAGAGATACTGTGTTGTTCAGGCTGGTCTCA A G ANKHD1-EIF4EBP3,ANKHD1 Ensembl:ENSG00000254996,Ensembl:ENSG00000131503 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs991414453 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_67656,RMVar_hsa_circ_120852,RMVar_hsa_circ_289834,RMVar_hsa_circ_351955,RMVar_hsa_circ_234972,RMVar_hsa_circ_342983,RMVar_hsa_circ_79657,RMVar_hsa_circ_56480,RMVar_hsa_circ_234973,RMVar_hsa_circ_34703,RMVar_hsa_circ_67499,RMVar_hsa_circ_234975,RMVar_hsa_circ_234974,RMVar_hsa_circ_277033,RMVar_hsa_circ_293937,RMVar_hsa_circ_355544,RMVar_hsa_circ_359829,RMVar_hsa_circ_334785,RMVar_hsa_circ_293305,RMVar_hsa_circ_78856,RMVar_hsa_circ_127717,RMVar_hsa_circ_58888,RMVar_hsa_circ_82652,RMVar_hsa_circ_234981,RMVar_hsa_circ_234982,RMVar_hsa_circ_234983,RMVar_hsa_circ_234980,RMVar_hsa_circ_336861,RMVar_hsa_circ_272566,RMVar_hsa_circ_286040,RMVar_hsa_circ_234984,RMVar_hsa_circ_355200,RMVar_hsa_circ_327100,RMVar_hsa_circ_275378,RMVar_hsa_circ_105324,RMVar_hsa_circ_125835,RMVar_hsa_circ_95890,RMVar_hsa_circ_234986,RMVar_hsa_circ_234990,RMVar_hsa_circ_14876,RMVar_hsa_circ_76845,RMVar_hsa_circ_234991,RMVar_hsa_circ_234992,RMVar_hsa_circ_234988,RMVar_hsa_circ_234989,RMVar_hsa_circ_234987,RMVar_hsa_circ_234985 51576 RMVar_ID_51576 Human_SNP_ID_253700300 A-to-I Human chr5 + 140469234 140469234 140469234 TTATCTACAAAAATCTTCTTGCCTGGCACAGTAGCTCAAGTCTTTAATCCCAGCTCTTTGGGAGG TTATCTACAAAAATCTTCTTGCCTGGCACAGTGGCTCAAGTCTTTAATCCCAGCTCTTTGGGAGG A G ANKHD1-EIF4EBP3,ANKHD1 Ensembl:ENSG00000254996,Ensembl:ENSG00000131503 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs543661763 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_21127716 RMVar_hsa_circ_120852,RMVar_hsa_circ_351955,RMVar_hsa_circ_234972,RMVar_hsa_circ_79657,RMVar_hsa_circ_56480,RMVar_hsa_circ_234973,RMVar_hsa_circ_67499,RMVar_hsa_circ_234974,RMVar_hsa_circ_355544,RMVar_hsa_circ_359829,RMVar_hsa_circ_334785,RMVar_hsa_circ_78856,RMVar_hsa_circ_127717,RMVar_hsa_circ_82652,RMVar_hsa_circ_234982,RMVar_hsa_circ_234983,RMVar_hsa_circ_327100,RMVar_hsa_circ_105324,RMVar_hsa_circ_125835,RMVar_hsa_circ_95890,RMVar_hsa_circ_234986,RMVar_hsa_circ_14876,RMVar_hsa_circ_76845,RMVar_hsa_circ_234988,RMVar_hsa_circ_234989,RMVar_hsa_circ_234987,RMVar_hsa_circ_123847,RMVar_hsa_circ_234985,RMVar_hsa_circ_378299,RMVar_hsa_circ_22963,RMVar_hsa_circ_53846,RMVar_hsa_circ_234993,RMVar_hsa_circ_61887,RMVar_hsa_circ_50297,RMVar_hsa_circ_14294,RMVar_hsa_circ_4962,RMVar_hsa_circ_353431,RMVar_hsa_circ_9404,RMVar_hsa_circ_325008,RMVar_hsa_circ_336364,RMVar_hsa_circ_92147,RMVar_hsa_circ_234995,RMVar_hsa_circ_234996,RMVar_hsa_circ_234997 51577 RMVar_ID_51577 Human_SNP_ID_253700348 A-to-I Human chr5 + 140469390 140469390 140469390 AAAATTAGCCGGGTGTGGTTGTGCGTGTCTGTAGTCCCAGCTACTCAGGAGGCTGAGGTGGATTG AAAATTAGCCGGGTGTGGTTGTGCGTGTCTGTTGTCCCAGCTACTCAGGAGGCTGAGGTGGATTG A T ANKHD1-EIF4EBP3,ANKHD1 Ensembl:ENSG00000254996,Ensembl:ENSG00000131503 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs937875235 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15326444 RMVar_hsa_circ_120852,RMVar_hsa_circ_351955,RMVar_hsa_circ_234972,RMVar_hsa_circ_79657,RMVar_hsa_circ_56480,RMVar_hsa_circ_234973,RMVar_hsa_circ_67499,RMVar_hsa_circ_234974,RMVar_hsa_circ_355544,RMVar_hsa_circ_359829,RMVar_hsa_circ_334785,RMVar_hsa_circ_78856,RMVar_hsa_circ_127717,RMVar_hsa_circ_82652,RMVar_hsa_circ_234982,RMVar_hsa_circ_234983,RMVar_hsa_circ_327100,RMVar_hsa_circ_105324,RMVar_hsa_circ_125835,RMVar_hsa_circ_95890,RMVar_hsa_circ_234986,RMVar_hsa_circ_14876,RMVar_hsa_circ_76845,RMVar_hsa_circ_234988,RMVar_hsa_circ_234989,RMVar_hsa_circ_234987,RMVar_hsa_circ_123847,RMVar_hsa_circ_234985,RMVar_hsa_circ_378299,RMVar_hsa_circ_22963,RMVar_hsa_circ_53846,RMVar_hsa_circ_234993,RMVar_hsa_circ_61887,RMVar_hsa_circ_50297,RMVar_hsa_circ_14294,RMVar_hsa_circ_4962,RMVar_hsa_circ_353431,RMVar_hsa_circ_9404,RMVar_hsa_circ_325008,RMVar_hsa_circ_336364,RMVar_hsa_circ_92147,RMVar_hsa_circ_234995,RMVar_hsa_circ_234996,RMVar_hsa_circ_234997 51578 RMVar_ID_51578 Human_SNP_ID_253713381 A-to-I Human chr5 + 140525326 140525323 140525326 CCTCTGCCACCCAGGCTGGAGTGCAGTGGTGCAATCTCGGCTCACTGCAACCTCTGCCCCCCAGG CCTCTGCCACCCAGGCTGGAGTGCAGTGGCGTGATCTCGGCTCACTGCAACCTCTGCCCCCCAGG TGCA CGTG ANKHD1-EIF4EBP3,ANKHD1 Ensembl:ENSG00000254996,Ensembl:ENSG00000131503 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs71588637 Functional Loss MNV dbSNP153 30..33 33 - - - 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_235019,RMVar_hsa_circ_373450,RMVar_hsa_circ_105948,RMVar_hsa_circ_57890,RMVar_hsa_circ_235020 51579 RMVar_ID_51579 Human_SNP_ID_253715973 A-to-I Human chr5 + 140535828 140535828 140535828 CCTGTAATCCCAGCACTTTGGGAGGCCTAGGCAAGAGGATCGCTTGAGCCCAGCAGTTGGAGACC CCTGTAATCCCAGCACTTTGGGAGGCCTAGGCCAGAGGATCGCTTGAGCCCAGCAGTTGGAGACC A C ANKHD1-EIF4EBP3,ANKHD1 Ensembl:ENSG00000254996,Ensembl:ENSG00000131503 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1457572115 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125835,RMVar_hsa_circ_234986,RMVar_hsa_circ_76845,RMVar_hsa_circ_234985,RMVar_hsa_circ_92147,RMVar_hsa_circ_234997,RMVar_hsa_circ_30477,RMVar_hsa_circ_26682,RMVar_hsa_circ_72161,RMVar_hsa_circ_60991 51580 RMVar_ID_51580 Human_SNP_ID_253716098 A-to-I Human chr5 + 140536337 140536337 140536337 GCTGGTCTCAAACTCCTAACCTTGGGTGGTCCACCTGCCTCAGCCTCCCAAAGTGCTGGGATTAC GCTGGTCTCAAACTCCTAACCTTGGGTGGTCCCCCTGCCTCAGCCTCCCAAAGTGCTGGGATTAC A C ANKHD1-EIF4EBP3,ANKHD1 Ensembl:ENSG00000254996,Ensembl:ENSG00000131503 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1173381020 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17575549 RMVar_hsa_circ_125835,RMVar_hsa_circ_234986,RMVar_hsa_circ_76845,RMVar_hsa_circ_234985,RMVar_hsa_circ_92147,RMVar_hsa_circ_234997,RMVar_hsa_circ_30477,RMVar_hsa_circ_26682,RMVar_hsa_circ_72161,RMVar_hsa_circ_60991 51581 RMVar_ID_51581 Human_SNP_ID_253716099 A-to-I Human chr5 + 140536346 140536346 140536346 AAACTCCTAACCTTGGGTGGTCCACCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG AAACTCCTAACCTTGGGTGGTCCACCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAG A G ANKHD1-EIF4EBP3,ANKHD1 Ensembl:ENSG00000254996,Ensembl:ENSG00000131503 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1429828804 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17575549 RMVar_hsa_circ_125835,RMVar_hsa_circ_234986,RMVar_hsa_circ_76845,RMVar_hsa_circ_234985,RMVar_hsa_circ_92147,RMVar_hsa_circ_234997,RMVar_hsa_circ_30477,RMVar_hsa_circ_26682,RMVar_hsa_circ_72161,RMVar_hsa_circ_60991 51582 RMVar_ID_51582 Human_SNP_ID_253716100 A-to-I Human chr5 + 140536368 140536351 140536368 CACCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCTGCCTGACCCCTTTGTT CACCTGCCTCAGCCTC_________________CAGGCGTGAGCCACCTGCCTGACCCCTTTGTT CCCAAAGTGCTGGGATTA C ANKHD1-EIF4EBP3,ANKHD1 Ensembl:ENSG00000254996,Ensembl:ENSG00000131503 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1263007462 Functional Loss DEL dbSNP153 17..33 33 - - - Human_RBP_ID_17575549 RMVar_hsa_circ_125835,RMVar_hsa_circ_234986,RMVar_hsa_circ_76845,RMVar_hsa_circ_234985,RMVar_hsa_circ_92147,RMVar_hsa_circ_234997,RMVar_hsa_circ_30477,RMVar_hsa_circ_26682,RMVar_hsa_circ_72161,RMVar_hsa_circ_60991 51583 RMVar_ID_51583 Human_SNP_ID_253716104 A-to-I Human chr5 + 140536368 140536368 140536368 CACCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCTGCCTGACCCCTTTGTT CACCTGCCTCAGCCTCCCAAAGTGCTGGGATTGCAGGCGTGAGCCACCTGCCTGACCCCTTTGTT A G ANKHD1-EIF4EBP3,ANKHD1 Ensembl:ENSG00000254996,Ensembl:ENSG00000131503 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1463817129 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17575549 RMVar_hsa_circ_125835,RMVar_hsa_circ_234986,RMVar_hsa_circ_76845,RMVar_hsa_circ_234985,RMVar_hsa_circ_92147,RMVar_hsa_circ_234997,RMVar_hsa_circ_30477,RMVar_hsa_circ_26682,RMVar_hsa_circ_72161,RMVar_hsa_circ_60991 51584 RMVar_ID_51584 Human_SNP_ID_253716206 A-to-I Human chr5 + 140536840 140536840 140536840 GAGGTTGGGAGTTTGAGACCAGCCTGACCAACATGGAGAAACCCGTCTCTACTAAAAATACAAAA GAGGTTGGGAGTTTGAGACCAGCCTGACCAACGTGGAGAAACCCGTCTCTACTAAAAATACAAAA A G ANKHD1-EIF4EBP3,ANKHD1 Ensembl:ENSG00000254996,Ensembl:ENSG00000131503 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs931367836 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125835,RMVar_hsa_circ_234986,RMVar_hsa_circ_76845,RMVar_hsa_circ_234985,RMVar_hsa_circ_92147,RMVar_hsa_circ_234997,RMVar_hsa_circ_30477,RMVar_hsa_circ_26682,RMVar_hsa_circ_72161,RMVar_hsa_circ_60991 51585 RMVar_ID_51585 Human_SNP_ID_253716233 A-to-I Human chr5 + 140536946 140536946 140536946 GGGAGGCTGAGGCAGGAGAATCGCTTGAACCCAGAAGGCAAAGGTTGCAGTGAGCCAAGATCACG GGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGGAAGGCAAAGGTTGCAGTGAGCCAAGATCACG A G ANKHD1-EIF4EBP3,ANKHD1 Ensembl:ENSG00000254996,Ensembl:ENSG00000131503 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1468027532 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_125835,RMVar_hsa_circ_234986,RMVar_hsa_circ_76845,RMVar_hsa_circ_234985,RMVar_hsa_circ_92147,RMVar_hsa_circ_234997,RMVar_hsa_circ_30477,RMVar_hsa_circ_26682,RMVar_hsa_circ_72161,RMVar_hsa_circ_60991 51586 RMVar_ID_51586 Human_SNP_ID_253718437 A-to-I Human chr5 + 140547025 140547025 140547025 CGCCTCCTGGGTTCAACCTATCCTTCCACCTCAGCTTCCCGAGTAGCTGGGTCTACAGGCGCATG CGCCTCCTGGGTTCAACCTATCCTTCCACCTCGGCTTCCCGAGTAGCTGGGTCTACAGGCGCATG A G ANKHD1-EIF4EBP3 Ensembl:ENSG00000254996 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1163738734 Functional Loss SNV dbSNP153 33..33 33 - - - 51587 RMVar_ID_51587 Human_SNP_ID_253718466 A-to-I Human chr5 + 140547128 140547126 140547128 CTAGGTTTCACCATGTTGCCCAGGCTGGTCTCAGACTCCTGGGCTCAAGCTATCCACCCGCCTTA CTAGGTTTCACCATGTTGCCCAGGCTGGTCT__GACTCCTGGGCTCAAGCTATCCACCCGCCTTA TCA T ANKHD1-EIF4EBP3 Ensembl:ENSG00000254996 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1242828184 Functional Loss DEL dbSNP153 32..33 33 - - - 51588 RMVar_ID_51588 Human_SNP_ID_253718467 A-to-I Human chr5 + 140547128 140547128 140547128 CTAGGTTTCACCATGTTGCCCAGGCTGGTCTCAGACTCCTGGGCTCAAGCTATCCACCCGCCTTA CTAGGTTTCACCATGTTGCCCAGGCTGGTCTCTGACTCCTGGGCTCAAGCTATCCACCCGCCTTA A T ANKHD1-EIF4EBP3 Ensembl:ENSG00000254996 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984516605 Functional Loss SNV dbSNP153 33..33 33 - - - 51589 RMVar_ID_51589 Human_SNP_ID_253746393 A-to-I Human chr5 + 140656332 140656332 140656332 CTCCTGCCGCAGCCTTCCAAGTAGCTGGGACTACAGGCATTCATCACCACACCTGGTTAATTTTT CTCCTGCCGCAGCCTTCCAAGTAGCTGGGACTGCAGGCATTCATCACCACACCTGGTTAATTTTT A G IK Ensembl:ENSG00000113141 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs913728045 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_76569,RMVar_hsa_circ_108069,RMVar_hsa_circ_235035,RMVar_hsa_circ_235036 51590 RMVar_ID_51590 Human_SNP_ID_253748730 A-to-I Human chr5 + 140665535 140665535 140665535 GCCCGCCACCACGCCCGGCTAATTTTTTTTGTATTTGTAGTAGAGACGGGGTTTCACCATCTTGG GCCCGCCACCACGCCCGGCTAATTTTTTTTGTGTTTGTAGTAGAGACGGGGTTTCACCATCTTGG A G WDR55 Ensembl:ENSG00000120314 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1390295092 Functional Loss SNV dbSNP153 33..33 33 - - - 51591 RMVar_ID_51591 Human_SNP_ID_253748821 A-to-I Human chr5 + 140665916 140665916 140665916 CCAGCTACACGGGAGGCTGAGGCAGAAGAATCACTTGGATTCGGGCGGTGGAGGTTGCAGTGAGC CCAGCTACACGGGAGGCTGAGGCAGAAGAATCGCTTGGATTCGGGCGGTGGAGGTTGCAGTGAGC A G WDR55 Ensembl:ENSG00000120314 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1180565203 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1319657 51592 RMVar_ID_51592 Human_SNP_ID_253753848 A-to-I Human chr5 - 140684243 140684241 140684243 CTCTGTCTCCCAGGCTGGAGTGCAGTGGCACTATCTCAGCTCACTGCAAGCTCCACCTGCCGGGT CTCTGTCTCCCAGGCTGGAGTGCAGTGGCACT__CTCAGCTCACTGCAAGCTCCACCTGCCGGGT GAT G HARS1 Ensembl:ENSG00000170445 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1263917821 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_90848,RMVar_hsa_circ_235049 51593 RMVar_ID_51593 Human_SNP_ID_253754407 A-to-I Human chr5 - 140686717 140686717 140686717 GCATGCTTGTAATGCCAGCTACTAGGGAAGCTAAGGCACAAGAATCGCTTGAACCTGGGAAGCAG GCATGCTTGTAATGCCAGCTACTAGGGAAGCTGAGGCACAAGAATCGCTTGAACCTGGGAAGCAG T C HARS1 Ensembl:ENSG00000170445 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs185440931 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_90848,RMVar_hsa_circ_235049 51594 RMVar_ID_51594 Human_SNP_ID_253802033 A-to-I Human chr5 + 140854001 140854000 140854001 TTGAGACCAATGTAGTGAGACTCATCTCTGCCAAAAAAAAAAAATTAGCCGGGCATGGTGGCACA TTGAGACCAATGTAGTGAGACTCATCTCTGCC_AAAAAAAAAAATTAGCCGGGCATGGTGGCACA CA C PCDHA5,PCDHA3,PCDHA4,PCDHA9,PCDHA7,PCDHA8,PCDHA1,PCDHA6,PCDHA2 Ensembl:ENSG00000204965,Ensembl:ENSG00000255408,Ensembl:ENSG00000204967,Ensembl:ENSG00000204961,Ensembl:ENSG00000204963,Ensembl:ENSG00000204962,Ensembl:ENSG00000204970,Ensembl:ENSG00000081842,Ensembl:ENSG00000204969 Protein coding,Protein coding,Protein coding,Protein coding,Protein coding,Protein coding,Protein coding,Protein coding,Protein coding intron,intron,intron,3'UTR,intron,intron,intron,intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs112540154 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_235058 51595 RMVar_ID_51595 Human_SNP_ID_253867440 A-to-I Human chr5 + 141123415 141123415 141123415 ACAACAGCCCCGCCCTGCACATCGGCAGTGTCAGCGCCACAGACAGAGACTCGGGCACCAACGCC ACAACAGCCCCGCCCTGCACATCGGCAGTGTCCGCGCCACAGACAGAGACTCGGGCACCAACGCC A C PCDHB4 Ensembl:ENSG00000081818 Protein coding exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs782542981 Functional Loss SNV dbSNP153,HGVD 33..33 33 - - - 51596 RMVar_ID_51596 Human_SNP_ID_253867441 A-to-I Human chr5 + 141123415 141123415 141123415 ACAACAGCCCCGCCCTGCACATCGGCAGTGTCAGCGCCACAGACAGAGACTCGGGCACCAACGCC ACAACAGCCCCGCCCTGCACATCGGCAGTGTCGGCGCCACAGACAGAGACTCGGGCACCAACGCC A G PCDHB4 Ensembl:ENSG00000081818 Protein coding exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs782542981 Functional Loss SNV dbSNP153 33..33 33 - - - 51597 RMVar_ID_51597 Human_SNP_ID_253867442 A-to-I Human chr5 + 141123415 141123415 141123415 ACAACAGCCCCGCCCTGCACATCGGCAGTGTCAGCGCCACAGACAGAGACTCGGGCACCAACGCC ACAACAGCCCCGCCCTGCACATCGGCAGTGTCTGCGCCACAGACAGAGACTCGGGCACCAACGCC A T PCDHB4 Ensembl:ENSG00000081818 Protein coding exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs782542981 Functional Loss SNV dbSNP153 33..33 33 - - - 51598 RMVar_ID_51598 Human_SNP_ID_253888886 A-to-I Human chr5 + 141190362 141190362 141190362 CACCACGTTCGGCTAATTTTTGTATTTTCAGTAGAGACGGGTTTCATCATGGTGGCCAGGATGGT CACCACGTTCGGCTAATTTTTGTATTTTCAGTGGAGACGGGTTTCATCATGGTGGCCAGGATGGT A G PCDHB9 Ensembl:ENSG00000177839 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1563948911 Functional Loss SNV dbSNP153 33..33 33 - - - 51599 RMVar_ID_51599 Human_SNP_ID_253888901 A-to-I Human chr5 + 141190449 141190449 141190449 ACCCCACTCAGCCTCCCAAATTGCTGGGATTTACAGGCATGAGCCACCGCACCCAGCCTACAATA ACCCCACTCAGCCTCCCAAATTGCTGGGATTTGCAGGCATGAGCCACCGCACCCAGCCTACAATA A G PCDHB9 Ensembl:ENSG00000177839 Protein coding 3'UTR GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1409501771 Functional Loss SNV dbSNP153 33..33 33 - - - 51600 RMVar_ID_51600 Human_SNP_ID_253925091 A-to-I Human chr5 - 141319173 141319173 141319173 AATTCAGAAGCAGATTGACAACATGAAAGGCAAGCTCCAAGAGACCCAGGACAGGGCAAAACGAC AATTCAGAAGCAGATTGACAACATGAAAGGCAGGCTCCAAGAGACCCAGGACAGGGCAAAACGAC T C TAF7 Ensembl:ENSG00000178913 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs780347920 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_78683,Human_RBP_ID_1646567,Human_RBP_ID_1988877,Human_RBP_ID_2901320,Human_RBP_ID_5151660,Human_RBP_ID_7395342,Human_RBP_ID_9398413,Human_RBP_ID_18537797,Human_RBP_ID_21214113,Human_RBP_ID_22099732,Human_RBP_ID_24548033,Human_RBP_ID_26351490,Human_RBP_ID_27075388,Human_RBP_ID_27825951 RMVar_hsa_circ_235070 51601 RMVar_ID_51601 Human_SNP_ID_253944409 A-to-I Human chr5 + 141377377 141377377 141377377 CCTGTAATCCCACCTCTTCAGGAGGCTGAGGCAGGAGGATCCCTTGAGACCAGGAGTTTGAGACC CCTGTAATCCCACCTCTTCAGGAGGCTGAGGCCGGAGGATCCCTTGAGACCAGGAGTTTGAGACC A C PCDHGB2,PCDHGA4,PCDHGA1,PCDHGA6,PCDHGB1,PCDHGB3,PCDHGA2,PCDHGA3,PCDHGA5 Ensembl:ENSG00000253910,Ensembl:ENSG00000262576,Ensembl:ENSG00000204956,Ensembl:ENSG00000253731,Ensembl:ENSG00000254221,Ensembl:ENSG00000262209,Ensembl:ENSG00000081853,Ensembl:ENSG00000254245,Ensembl:ENSG00000253485 Protein coding,Protein coding,Protein coding,Protein coding,Protein coding,Protein coding,Protein coding,Protein coding,Protein coding intron,intron,intron,intron,intron,intron,intron,intron,intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs761434050 Functional Loss SNV dbSNP153 33..33 33 - - - 51602 RMVar_ID_51602 Human_SNP_ID_253968957 A-to-I Human chr5 + 141458633 141458633 141458633 ACTCTGTCAGCCAGGCTGGAGTGCAGTGGCACAATCCCAGCTCACTGCAACCTCCACCTCTCGGG ACTCTGTCAGCCAGGCTGGAGTGCAGTGGCACCATCCCAGCTCACTGCAACCTCCACCTCTCGGG A C PCDHGA4,PCDHGA2,PCDHGB2,PCDHGA8,PCDHGB6,PCDHGB4,PCDHGA1,PCDHGB5,PCDHGA6,PCDHGA12,PCDHGA10,PCDHGA7,PCDHGB1,PCDHGB3,PCDHGA9,PCDHGB7,PCDHGA11,PCDHGA3,PCDHGA5 Ensembl:ENSG00000262576,Ensembl:ENSG00000081853,Ensembl:ENSG00000253910,Ensembl:ENSG00000253767,Ensembl:ENSG00000253305,Ensembl:ENSG00000253953,Ensembl:ENSG00000204956,Ensembl:ENSG00000276547,Ensembl:ENSG00000253731,Ensembl:ENSG00000253159,Ensembl:ENSG00000253846,Ensembl:ENSG00000253537,Ensembl:ENSG00000254221,Ensembl:ENSG00000262209,Ensembl:ENSG00000261934,Ensembl:ENSG00000254122,Ensembl:ENSG00000253873,Ensembl:ENSG00000254245,Ensembl:ENSG00000253485 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,Protein coding,Protein coding,Protein coding,Protein coding intron,intron,intron,intron,intron,intron,intron,intron,intron,intron,intron,intron,intron,intron,intron,intron,intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs548586597 Functional Loss SNV dbSNP153 33..33 33 - - - 51603 RMVar_ID_51603 Human_SNP_ID_253986139 A-to-I Human chr5 - 141526772 141526772 141526772 GAATTGCTTGAACCCAGGAGGTGGAGGTTGCAATGAGCCAAGATCGCGCCACTGCACTCCTGCCC GAATTGCTTGAACCCAGGAGGTGGAGGTTGCAGTGAGCCAAGATCGCGCCACTGCACTCCTGCCC T C DIAPH1 Ensembl:ENSG00000131504 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1211361612 Functional Loss SNV dbSNP153 33..33 33 - - - 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_58462,RMVar_hsa_circ_91511,RMVar_hsa_circ_235088,RMVar_hsa_circ_42805,RMVar_hsa_circ_235090 51604 RMVar_ID_51604 Human_SNP_ID_253986244 A-to-I Human chr5 - 141527293 141527293 141527293 TTACCCCCTCAGCCTCCTTGGTAGCTGGGACTACAGGCATGTGCCACCAGGCCCTGCTAAACTTT TTACCCCCTCAGCCTCCTTGGTAGCTGGGACTGCAGGCATGTGCCACCAGGCCCTGCTAAACTTT T C DIAPH1 Ensembl:ENSG00000131504 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1251895278 Functional Loss SNV dbSNP153 33..33 33 - - - 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_58462,RMVar_hsa_circ_91511,RMVar_hsa_circ_235088,RMVar_hsa_circ_42805,RMVar_hsa_circ_235090 51605 RMVar_ID_51605 Human_SNP_ID_253987305 A-to-I Human chr5 - 141531378 141531378 141531378 TTGAGGCTGGGAGGTCCAGGCTGCCATGAGCTATGACTGCACTGCTGCACTCTAGCTTGGGCAAC TTGAGGCTGGGAGGTCCAGGCTGCCATGAGCTGTGACTGCACTGCTGCACTCTAGCTTGGGCAAC T C DIAPH1 Ensembl:ENSG00000131504 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs554703145 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_25864781 RMVar_hsa_circ_97418,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_235085,RMVar_hsa_circ_235082,RMVar_hsa_circ_235083,RMVar_hsa_circ_235081,RMVar_hsa_circ_235078,RMVar_hsa_circ_235079,RMVar_hsa_circ_52474,RMVar_hsa_circ_91511,RMVar_hsa_circ_235088,RMVar_hsa_circ_235090,RMVar_hsa_circ_99524,RMVar_hsa_circ_235091 51606 RMVar_ID_51606 Human_SNP_ID_253987324 A-to-I Human chr5 - 141531453 141531453 141531453 AAAAAACTAGCCAGATGTGGTGCCGCATGCCTATAGTCCCAGCCACTTGGGAGACTGAGGTGGGT AAAAAACTAGCCAGATGTGGTGCCGCATGCCTGTAGTCCCAGCCACTTGGGAGACTGAGGTGGGT T C DIAPH1 Ensembl:ENSG00000131504 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs936049493 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97418,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_235085,RMVar_hsa_circ_235082,RMVar_hsa_circ_235083,RMVar_hsa_circ_235081,RMVar_hsa_circ_235078,RMVar_hsa_circ_235079,RMVar_hsa_circ_52474,RMVar_hsa_circ_91511,RMVar_hsa_circ_235088,RMVar_hsa_circ_235090,RMVar_hsa_circ_99524,RMVar_hsa_circ_235091 51607 RMVar_ID_51607 Human_SNP_ID_253992248 A-to-I Human chr5 - 141551369 141551369 141551369 ACACTGTAACCTTGAACTCCCTGGCACAAGCAATCCTTTCACCTCAGCCTTCTGAGTAACTGGGA ACACTGTAACCTTGAACTCCCTGGCACAAGCAGTCCTTTCACCTCAGCCTTCTGAGTAACTGGGA T C DIAPH1 Ensembl:ENSG00000131504 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs748643366 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97418,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_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_235088,RMVar_hsa_circ_235090,RMVar_hsa_circ_99524,RMVar_hsa_circ_235091,RMVar_hsa_circ_110882,RMVar_hsa_circ_127283,RMVar_hsa_circ_53490,RMVar_hsa_circ_348962,RMVar_hsa_circ_119447,RMVar_hsa_circ_235092,RMVar_hsa_circ_235093,RMVar_hsa_circ_235094 51608 RMVar_ID_51608 Human_SNP_ID_254003073 A-to-I Human chr5 - 141594507 141594507 141594507 AACCTCCTGGTCTCAAGTAACCCACCCGTCTCAGCCTCCCAGAGTGCCATGTTTACAGGTGTGAG AACCTCCTGGTCTCAAGTAACCCACCCGTCTCCGCCTCCCAGAGTGCCATGTTTACAGGTGTGAG T G DIAPH1 Ensembl:ENSG00000131504 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1279884633 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_85703,RMVar_hsa_circ_235098,RMVar_hsa_circ_94492,RMVar_hsa_circ_235104 51609 RMVar_ID_51609 Human_SNP_ID_254022298 A-to-I Human chr5 - 141667885 141667885 141667885 GGCGCACATGACCTCGCCCGGCTAATTTTTGTATTTTTGGTAGAGATGGGGTTTCACCATGTTGG GGCGCACATGACCTCGCCCGGCTAATTTTTGTGTTTTTGGTAGAGATGGGGTTTCACCATGTTGG T C ARAP3 Ensembl:ENSG00000120318 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1051116102 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_91570,RMVar_hsa_circ_86058,RMVar_hsa_circ_235120,RMVar_hsa_circ_235123 51610 RMVar_ID_51610 Human_SNP_ID_254102622 A-to-I Human chr5 + 141990541 141990541 141990541 CCATGCCCAGCTAATTTTTTTTTTTTCTTTTTAGTAGAAATAAGGTCTCGCTATATTGCCCAGGT CCATGCCCAGCTAATTTTTTTTTTTTCTTTTTTGTAGAAATAAGGTCTCGCTATATTGCCCAGGT A T RF00017-4633 RNACentral:URS00009644F0 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1349316499 Functional Loss SNV dbSNP153 33..33 33 - - - 51611 RMVar_ID_51611 Human_SNP_ID_254138731 A-to-I Human chr5 + 142137451 142137451 142137451 GGGATCCTCCAACGTTGGCCTCCCAAAGTGCTAGGATTACAGATGTGAGCTATTGTGCTCAGCCT GGGATCCTCCAACGTTGGCCTCCCAAAGTGCTGGGATTACAGATGTGAGCTATTGTGCTCAGCCT A G NDFIP1 Ensembl:ENSG00000131507 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232138427 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_235153,RMVar_hsa_circ_323924,RMVar_hsa_circ_282546,RMVar_hsa_circ_272303,RMVar_hsa_circ_235151,RMVar_hsa_circ_235152,RMVar_hsa_circ_235150,RMVar_hsa_circ_336380,RMVar_hsa_circ_235159,RMVar_hsa_circ_235157,RMVar_hsa_circ_278409,RMVar_hsa_circ_313650,RMVar_hsa_circ_272655 51612 RMVar_ID_51612 Human_SNP_ID_254139855 A-to-I Human chr5 + 142141994 142141994 142141994 CGTCTCTACAAAAAAATTTTTTTAAATTAACCAAGCATGGTGGTTTGTGCCTGTAGTCCTAGCTA CGTCTCTACAAAAAAATTTTTTTAAATTAACCGAGCATGGTGGTTTGTGCCTGTAGTCCTAGCTA A G NDFIP1 Ensembl:ENSG00000131507 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1014810956 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_282546,RMVar_hsa_circ_235151,RMVar_hsa_circ_235150,RMVar_hsa_circ_336380,RMVar_hsa_circ_235157,RMVar_hsa_circ_313650,RMVar_hsa_circ_342957 51613 RMVar_ID_51613 Human_SNP_ID_254139862 A-to-I Human chr5 + 142142016 142142016 142142016 TAAATTAACCAAGCATGGTGGTTTGTGCCTGTAGTCCTAGCTACTTGGGAGACTGAGCCAGGAGG TAAATTAACCAAGCATGGTGGTTTGTGCCTGTGGTCCTAGCTACTTGGGAGACTGAGCCAGGAGG A G NDFIP1 Ensembl:ENSG00000131507 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs576583844 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15332283 RMVar_hsa_circ_282546,RMVar_hsa_circ_235151,RMVar_hsa_circ_235150,RMVar_hsa_circ_336380,RMVar_hsa_circ_235157,RMVar_hsa_circ_313650,RMVar_hsa_circ_342957 51614 RMVar_ID_51614 Human_SNP_ID_254140032 A-to-I Human chr5 + 142142781 142142781 142142781 GAAACCCCGTCTCTACTAAAAATACAAAAATTAGCTGGCTGTGGTTGCTCATGCCTATGATCCCA GAAACCCCGTCTCTACTAAAAATACAAAAATTTGCTGGCTGTGGTTGCTCATGCCTATGATCCCA A T NDFIP1 Ensembl:ENSG00000131507 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1250499736 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15332313 RMVar_hsa_circ_282546,RMVar_hsa_circ_235151,RMVar_hsa_circ_235150,RMVar_hsa_circ_336380,RMVar_hsa_circ_235157,RMVar_hsa_circ_313650,RMVar_hsa_circ_235160,RMVar_hsa_circ_342957 51615 RMVar_ID_51615 Human_SNP_ID_254394612 A-to-I Human chr5 + 143199814 143199814 143199814 CCAAAGTCTGACACTGTGGAGACTCTTAGTGCAAGACTCTCAGGCCCTTCCTTGTGTGCCTTATC CCAAAGTCTGACACTGTGGAGACTCTTAGTGCGAGACTCTCAGGCCCTTCCTTGTGTGCCTTATC A G ARHGAP26 Ensembl:ENSG00000145819 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1360029392 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1390442 RMVar_hsa_circ_83765,RMVar_hsa_circ_235191 51616 RMVar_ID_51616 Human_SNP_ID_254397491 A-to-I Human chr5 + 143211795 143211795 143211795 TCTCTACAGTCTGGTCTTAAATTCCTGGGCTCAAGCAATCCTCCCACCTCCCAAAGTGCTAGGAT TCTCTACAGTCTGGTCTTAAATTCCTGGGCTCCAGCAATCCTCCCACCTCCCAAAGTGCTAGGAT A C ARHGAP26 Ensembl:ENSG00000145819 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1228974461 Functional Loss SNV dbSNP153 33..33 33 - - - 51617 RMVar_ID_51617 Human_SNP_ID_254400749 A-to-I Human chr5 + 143225349 143225349 143225349 AGCTGGGACTACAGGCATGAGCCATCACACCCAGCTAGTTTTTTGTATTTTTAGTAAAGATGGGG AGCTGGGACTACAGGCATGAGCCATCACACCCGGCTAGTTTTTTGTATTTTTAGTAAAGATGGGG A G ARHGAP26 Ensembl:ENSG00000145819 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1279725088 Functional Loss SNV dbSNP153 33..33 33 - - - 51618 RMVar_ID_51618 Human_SNP_ID_254400940 A-to-I Human chr5 + 143226210 143226210 143226210 TTTCGTAGCTAAAGAATGCCATGGCCGGGTGCAGTGGCTCACGCCTATAATCCCAGCACTTTGGG TTTCGTAGCTAAAGAATGCCATGGCCGGGTGCGGTGGCTCACGCCTATAATCCCAGCACTTTGGG A G ARHGAP26 Ensembl:ENSG00000145819 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs951602125 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_621842 51619 RMVar_ID_51619 Human_SNP_ID_254400947 A-to-I Human chr5 + 143226224 143226224 143226224 AATGCCATGGCCGGGTGCAGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCCGAGGCGGGC AATGCCATGGCCGGGTGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGC A G ARHGAP26 Ensembl:ENSG00000145819 Protein coding 3'UTR GSE38233;GSE107867 cultured B-cells;ASD brains,frontal_cortex - 24183664,30559470 RNA-Seq:(High) rs1166573583 Functional Loss SNV dbSNP153 33..33 33 - - - 51620 RMVar_ID_51620 Human_SNP_ID_254400984 A-to-I Human chr5 + 143226318 143226318 143226318 CCTGGCTACGACGGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTAGCCGGGTGTGGTGGCG CCTGGCTACGACGGTGAAACCCCGTCTCTACTGAAAATACAAAAAATTAGCCGGGTGTGGTGGCG A G ARHGAP26 Ensembl:ENSG00000145819 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1378550310 Functional Loss SNV dbSNP153 33..33 33 - - - 51621 RMVar_ID_51621 Human_SNP_ID_254401007 A-to-I Human chr5 + 143226401 143226401 143226401 TACTCTGGAGGCTGAGGCAGGAGAATGGCATGAACCCAGGAGGCAGAGATTGCAGTGAGCCAAGA TACTCTGGAGGCTGAGGCAGGAGAATGGCATGCACCCAGGAGGCAGAGATTGCAGTGAGCCAAGA A C ARHGAP26 Ensembl:ENSG00000145819 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1054140445 Functional Loss SNV dbSNP153 33..33 33 - - - 51622 RMVar_ID_51622 Human_SNP_ID_254401012 A-to-I Human chr5 + 143226430 143226430 143226430 ATGAACCCAGGAGGCAGAGATTGCAGTGAGCCAAGATCACGCCCCTGCACTCCAGCCTGGGTGAC ATGAACCCAGGAGGCAGAGATTGCAGTGAGCCGAGATCACGCCCCTGCACTCCAGCCTGGGTGAC A G ARHGAP26 Ensembl:ENSG00000145819 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs369614922 Functional Loss SNV dbSNP153 33..33 33 - - - 51623 RMVar_ID_51623 Human_SNP_ID_254401013 A-to-I Human chr5 + 143226433 143226433 143226433 AACCCAGGAGGCAGAGATTGCAGTGAGCCAAGATCACGCCCCTGCACTCCAGCCTGGGTGACAGA AACCCAGGAGGCAGAGATTGCAGTGAGCCAAGTTCACGCCCCTGCACTCCAGCCTGGGTGACAGA A T ARHGAP26 Ensembl:ENSG00000145819 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1413727097 Functional Loss SNV dbSNP153 33..33 33 - - - 51624 RMVar_ID_51624 Human_SNP_ID_254415940 A-to-I Human chr5 - 143288548 143288548 143288548 AGGTCAAGGCTGCAGTGAGCCATGATCATGCCAGTGCACTCTAGCCTGGGCAACAGAGTGAGACT AGGTCAAGGCTGCAGTGAGCCATGATCATGCCGGTGCACTCTAGCCTGGGCAACAGAGTGAGACT T C NR3C1 Ensembl:ENSG00000113580 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1360255785 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23314263 RMVar_hsa_circ_74142,RMVar_hsa_circ_98442,RMVar_hsa_circ_235196,RMVar_hsa_circ_68464 51625 RMVar_ID_51625 Human_SNP_ID_254415956 A-to-I Human chr5 - 143288632 143288632 143288632 CCTGTCACTACACAAAATAGAAAAAATTAGCCAGGCATGGTAGCTTGTGCCTGTAGTCCCAGCTA CCTGTCACTACACAAAATAGAAAAAATTAGCCGGGCATGGTAGCTTGTGCCTGTAGTCCCAGCTA T C NR3C1 Ensembl:ENSG00000113580 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs912292037 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74142,RMVar_hsa_circ_98442,RMVar_hsa_circ_235196,RMVar_hsa_circ_68464 51626 RMVar_ID_51626 Human_SNP_ID_254416041 A-to-I Human chr5 - 143289010 143289010 143289010 TGGAGTGCAGTGGCATGATCTTGGCTCATCGCAGCCTCAGCCTCCCCAGCAGTGGGATTGCAGGC TGGAGTGCAGTGGCATGATCTTGGCTCATCGCGGCCTCAGCCTCCCCAGCAGTGGGATTGCAGGC T C NR3C1 Ensembl:ENSG00000113580 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs905288425 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74142,RMVar_hsa_circ_98442,RMVar_hsa_circ_235196,RMVar_hsa_circ_68464 51627 RMVar_ID_51627 Human_SNP_ID_254416042 A-to-I Human chr5 - 143289010 143289010 143289010 TGGAGTGCAGTGGCATGATCTTGGCTCATCGCAGCCTCAGCCTCCCCAGCAGTGGGATTGCAGGC TGGAGTGCAGTGGCATGATCTTGGCTCATCGCCGCCTCAGCCTCCCCAGCAGTGGGATTGCAGGC T G NR3C1 Ensembl:ENSG00000113580 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs905288425 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74142,RMVar_hsa_circ_98442,RMVar_hsa_circ_235196,RMVar_hsa_circ_68464 51628 RMVar_ID_51628 Human_SNP_ID_254420549 A-to-I Human chr5 - 143308388 143308388 143308388 ATGAACATGGCTCACTGCAGCCTTGAACTCCTAGACTCAAGCCATCTTCCCACCCAGTAGGGCTA ATGAACATGGCTCACTGCAGCCTTGAACTCCTGGACTCAAGCCATCTTCCCACCCAGTAGGGCTA T C NR3C1 Ensembl:ENSG00000113580 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1400725458 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12951,RMVar_hsa_circ_74142,RMVar_hsa_circ_68464,RMVar_hsa_circ_267895,RMVar_hsa_circ_327282,RMVar_hsa_circ_278516,RMVar_hsa_circ_126728,RMVar_hsa_circ_235198,RMVar_hsa_circ_235199 51629 RMVar_ID_51629 Human_SNP_ID_254421665 A-to-I Human chr5 - 143312961 143312961 143312961 GCAAATTATAAAATTACTCATATTACACCACAAAGATTACAAGGATGGCAGCTTTGGCCAGTGTA GCAAATTATAAAATTACTCATATTACACCACAGAGATTACAAGGATGGCAGCTTTGGCCAGTGTA T C NR3C1 Ensembl:ENSG00000113580 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1409689755 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74142,RMVar_hsa_circ_68464,RMVar_hsa_circ_267895,RMVar_hsa_circ_327282,RMVar_hsa_circ_278516,RMVar_hsa_circ_332106,RMVar_hsa_circ_126728,RMVar_hsa_circ_235198,RMVar_hsa_circ_235199,RMVar_hsa_circ_332835 51630 RMVar_ID_51630 Human_SNP_ID_254428818 A-to-I Human chr5 - 143345456 143345456 143345456 TCTGTAATCCCGGCACTTTGGGAGGCCAAGGCAGGCGGGTCACTGGAGGTCAGGAGTTCAACACC TCTGTAATCCCGGCACTTTGGGAGGCCAAGGCCGGCGGGTCACTGGAGGTCAGGAGTTCAACACC T G NR3C1 Ensembl:ENSG00000113580 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1361585060 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_74142,RMVar_hsa_circ_327282,RMVar_hsa_circ_332106,RMVar_hsa_circ_126728,RMVar_hsa_circ_235199 51631 RMVar_ID_51631 Human_SNP_ID_254631613 A-to-I Human chr5 - 144160234 144160234 144160234 GTAAACGTGTATCTCTTGTTCATTTTTATAGAACTTTTGCATACTATATTGGATTTACCTGCGGT GTAAACGTGTATCTCTTGTTCATTTTTATAGAGCTTTTGCATACTATATTGGATTTACCTGCGGT T C YIPF5 Ensembl:ENSG00000145817 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs542441558 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1319880,Human_RBP_ID_1646888,Human_RBP_ID_1989399,Human_RBP_ID_2904133,Human_RBP_ID_3761143,Human_RBP_ID_8885756,Human_RBP_ID_9171274,Human_RBP_ID_15336158,Human_RBP_ID_17527995,Human_RBP_ID_24504045,Human_RBP_ID_27075641 Human_miRNA_ID_154191 RMVar_hsa_circ_113124,RMVar_hsa_circ_122491,RMVar_hsa_circ_235204,RMVar_hsa_circ_75696,RMVar_hsa_circ_235205,RMVar_hsa_circ_235203 51632 RMVar_ID_51632 Human_SNP_ID_254646595 A-to-I Human chr5 + 144222732 144222732 144222732 TAAACTAGTTCAACCATTGTGGAAGACAGCGTAGCGATTCCTCAAATATCCAGAACTAGAAATAC TAAACTAGTTCAACCATTGTGGAAGACAGCGTGGCGATTCCTCAAATATCCAGAACTAGAAATAC A G KCTD16 Ensembl:ENSG00000183775 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs921810331 Functional Loss SNV dbSNP153 33..33 33 - - - 51633 RMVar_ID_51633 Human_SNP_ID_254648273 A-to-I Human chr5 + 144230008 144230008 144230008 TACTAAAAATACAAAAATCAGCTGGACATGGTAGCTTGTGCCTGTGGTCCTAGCTACATGGGAGG TACTAAAAATACAAAAATCAGCTGGACATGGTGGCTTGTGCCTGTGGTCCTAGCTACATGGGAGG A G KCTD16 Ensembl:ENSG00000183775 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1024976102 Functional Loss SNV dbSNP153 33..33 33 - - - 51634 RMVar_ID_51634 Human_SNP_ID_254651026 A-to-I Human chr5 + 144242575 144242575 144242575 GTTATTGTCTTAGTCCATTTTGTGTTGCTATAAAGAAATACTTAAGCCTGGGTAATTTATACAGA GTTATTGTCTTAGTCCATTTTGTGTTGCTATAGAGAAATACTTAAGCCTGGGTAATTTATACAGA A G KCTD16 Ensembl:ENSG00000183775 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs868300287 Functional Loss SNV dbSNP153 33..33 33 - - - 51635 RMVar_ID_51635 Human_SNP_ID_254980412 A-to-I Human chr5 - 145502103 145502103 145502103 TCCTGTAGAGCCTGCAGAACTGTGAGCCAATTAAACCTCTTTTCTTTATAAATTACTCAGTCTCA TCCTGTAGAGCCTGCAGAACTGTGAGCCAATTGAACCTCTTTTCTTTATAAATTACTCAGTCTCA T C PRELID2 Ensembl:ENSG00000186314 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264259130 Functional Loss SNV dbSNP153 33..33 33 - - - 51636 RMVar_ID_51636 Human_SNP_ID_255125215 A-to-I Human chr5 - 146091720 146091720 146091720 ACAGCTCATTGTAACCGCGGACTTCTAGGTTCAAGTGATCCTCTTGCCTCAGCCTCTAGAGTGGC ACAGCTCATTGTAACCGCGGACTTCTAGGTTCTAGTGATCCTCTTGCCTCAGCCTCTAGAGTGGC T A PLAC8L1 Ensembl:ENSG00000173261 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs747551717 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64064 51637 RMVar_ID_51637 Human_SNP_ID_255126910 A-to-I Human chr5 - 146099436 146099436 146099436 CAGGCGGTCTTGAACTCCTGACCTCATGATCCACCCACCTCAGGCTCCCAAAGTGCTGGGATTAC CAGGCGGTCTTGAACTCCTGACCTCATGATCCTCCCACCTCAGGCTCCCAAAGTGCTGGGATTAC T A PLAC8L1 Ensembl:ENSG00000173261 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1013282799 Functional Loss SNV dbSNP153 33..33 33 - - - 51638 RMVar_ID_51638 Human_SNP_ID_255127277 A-to-I Human chr5 - 146100937 146100937 146100937 CCTTAGCCTCCCAAAGTGCTGGGATTATAGGCATGAGCCACTGTGCCTGGCCTAAGGCCACCAAA CCTTAGCCTCCCAAAGTGCTGGGATTATAGGCGTGAGCCACTGTGCCTGGCCTAAGGCCACCAAA T C PLAC8L1 Ensembl:ENSG00000173261 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1399632481 Functional Loss SNV dbSNP153 33..33 33 - - - 51639 RMVar_ID_51639 Human_SNP_ID_255127312 A-to-I Human chr5 - 146101089 146101089 146101089 AGGCTCAAGCAATCCTTCTACGTTAGCTTCCCAAGTAGCTGAGACCACAGGTGCGTGCCACCATG AGGCTCAAGCAATCCTTCTACGTTAGCTTCCCGAGTAGCTGAGACCACAGGTGCGTGCCACCATG T C PLAC8L1 Ensembl:ENSG00000173261 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1244107705 Functional Loss SNV dbSNP153 33..33 33 - - - 51640 RMVar_ID_51640 Human_SNP_ID_255130243 A-to-I Human chr5 - 146113170 146113170 146113170 ATCCCAGCTGCTTGGGAGTGTGAGGCAGGAGAATCGCTTGAACCTGGGAGACCGAGGTTGCAGTG ATCCCAGCTGCTTGGGAGTGTGAGGCAGGAGAGTCGCTTGAACCTGGGAGACCGAGGTTGCAGTG T C LARS1 Ensembl:ENSG00000133706 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs993108444 Functional Loss SNV dbSNP153 33..33 33 - - - 51641 RMVar_ID_51641 Human_SNP_ID_255134633 A-to-I Human chr5 - 146131552 146131552 146131552 AGGAGTTTGAGGCTGCAGTGAGTTGTGATCATACCACTGCATTCTAGCCTAGGTGACAGAGACCC AGGAGTTTGAGGCTGCAGTGAGTTGTGATCATTCCACTGCATTCTAGCCTAGGTGACAGAGACCC T A LARS1 Ensembl:ENSG00000133706 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1038594062 Functional Loss SNV dbSNP153 33..33 33 - - - 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 51642 RMVar_ID_51642 Human_SNP_ID_255134705 A-to-I Human chr5 - 146131782 146131782 146131782 ATGCAATAATTAAAACCTGGCTATGGCCAGGCACTGTGGCTCACGCCTGTAAACCAGGCACTTTG ATGCAATAATTAAAACCTGGCTATGGCCAGGCGCTGTGGCTCACGCCTGTAAACCAGGCACTTTG T C LARS1 Ensembl:ENSG00000133706 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs992211021 Functional Loss SNV dbSNP153 33..33 33 - - - 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 51643 RMVar_ID_51643 Human_SNP_ID_255134782 A-to-I Human chr5 - 146132142 146132142 146132142 ACCACGTCTGGCCAATTTTTTGTATTTTTAGTAGAGATGGGGTTTCACTGTGTTGGCCAGGCTGG ACCACGTCTGGCCAATTTTTTGTATTTTTAGTGGAGATGGGGTTTCACTGTGTTGGCCAGGCTGG T C LARS1 Ensembl:ENSG00000133706 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1039458565 Functional Loss SNV dbSNP153 33..33 33 - - - 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 51644 RMVar_ID_51644 Human_SNP_ID_255134785 A-to-I Human chr5 - 146132160 146132160 146132160 GGATTACAGGTGCCTGCCACCACGTCTGGCCAATTTTTTGTATTTTTAGTAGAGATGGGGTTTCA GGATTACAGGTGCCTGCCACCACGTCTGGCCATTTTTTTGTATTTTTAGTAGAGATGGGGTTTCA T A LARS1 Ensembl:ENSG00000133706 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs938353983 Functional Loss SNV dbSNP153 33..33 33 - - - 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 51645 RMVar_ID_51645 Human_SNP_ID_255134786 A-to-I Human chr5 - 146132160 146132160 146132160 GGATTACAGGTGCCTGCCACCACGTCTGGCCAATTTTTTGTATTTTTAGTAGAGATGGGGTTTCA GGATTACAGGTGCCTGCCACCACGTCTGGCCAGTTTTTTGTATTTTTAGTAGAGATGGGGTTTCA T C LARS1 Ensembl:ENSG00000133706 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs938353983 Functional Loss SNV dbSNP153 33..33 33 - - - 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 51646 RMVar_ID_51646 Human_SNP_ID_255134791 A-to-I Human chr5 - 146132187 146132187 146132187 CTTCTGCCCCAGCCTCCCTACTAGCTGGGATTACAGGTGCCTGCCACCACGTCTGGCCAATTTTT CTTCTGCCCCAGCCTCCCTACTAGCTGGGATTGCAGGTGCCTGCCACCACGTCTGGCCAATTTTT T C LARS1 Ensembl:ENSG00000133706 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs747095326 Functional Loss SNV dbSNP153 33..33 33 - - - 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 51647 RMVar_ID_51647 Human_SNP_ID_255134806 A-to-I Human chr5 - 146132266 146132266 146132266 GAGTCTCGCACTGTCACTCAGGCTGGAGTGCAATGGCACAATCTCAGCTCACTGCAGCCTCTGCC GAGTCTCGCACTGTCACTCAGGCTGGAGTGCAGTGGCACAATCTCAGCTCACTGCAGCCTCTGCC T C LARS1 Ensembl:ENSG00000133706 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1013573560 Functional Loss SNV dbSNP153 33..33 33 - - - 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 51648 RMVar_ID_51648 Human_SNP_ID_255136017 A-to-I Human chr5 - 146137173 146137173 146137173 TTGTAGGGGACTGGGCGCGGTGACTCACGCCTATAATCCCAGCACTTTGGGAGGCCAAGGCGGGT TTGTAGGGGACTGGGCGCGGTGACTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGT T C LARS1 Ensembl:ENSG00000133706 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs776902224 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15338946 RMVar_hsa_circ_59893,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_109680,RMVar_hsa_circ_235233,RMVar_hsa_circ_100747,RMVar_hsa_circ_20383,RMVar_hsa_circ_235238,RMVar_hsa_circ_235234,RMVar_hsa_circ_235235,RMVar_hsa_circ_235236,RMVar_hsa_circ_104530,RMVar_hsa_circ_369997,RMVar_hsa_circ_235237 51649 RMVar_ID_51649 Human_SNP_ID_255138222 A-to-I Human chr5 - 146145154 146145151 146145154 AAGGGTCACATGAGCCAGGAGGTCGAGGTTGTAGTGAGCCATGATAGTGCCACTGCGCTCCAGCC AAGGGTCACATGAGCCAGGAGGTCGAGGTTGT___GAGCCATGATAGTGCCACTGCGCTCCAGCC CACT C LARS1 Ensembl:ENSG00000133706 Protein coding exon GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1206156402 Functional Loss DEL dbSNP153 33..35 33 - - - Human_RBP_ID_7400595,Human_RBP_ID_8606346,Human_RBP_ID_15339294 RMVar_hsa_circ_265072,RMVar_hsa_circ_100747,RMVar_hsa_circ_235238,RMVar_hsa_circ_235236,RMVar_hsa_circ_104530,RMVar_hsa_circ_82362,RMVar_hsa_circ_235241,RMVar_hsa_circ_45752,RMVar_hsa_circ_59644,RMVar_hsa_circ_93600,RMVar_hsa_circ_113570,RMVar_hsa_circ_235243,RMVar_hsa_circ_235244,RMVar_hsa_circ_123626,RMVar_hsa_circ_235245 51650 RMVar_ID_51650 Human_SNP_ID_255138269 A-to-I Human chr5 - 146145354 146145354 146145354 CCATAGGGCTGTGCACAGTGGCTCAAGGCTGTAATCCAAACACTTTGGGAGGCTGAGGTGGAATA CCATAGGGCTGTGCACAGTGGCTCAAGGCTGTGATCCAAACACTTTGGGAGGCTGAGGTGGAATA T C LARS1 Ensembl:ENSG00000133706 Protein coding exon GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1019483032 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7400597,Human_RBP_ID_15339304 RMVar_hsa_circ_265072,RMVar_hsa_circ_100747,RMVar_hsa_circ_235238,RMVar_hsa_circ_235236,RMVar_hsa_circ_104530,RMVar_hsa_circ_82362,RMVar_hsa_circ_235241,RMVar_hsa_circ_45752,RMVar_hsa_circ_59644,RMVar_hsa_circ_93600,RMVar_hsa_circ_113570,RMVar_hsa_circ_235243,RMVar_hsa_circ_235244,RMVar_hsa_circ_123626,RMVar_hsa_circ_235245 51651 RMVar_ID_51651 Human_SNP_ID_255138404 A-to-I Human chr5 - 146146158 146146158 146146158 TTTTGTATTTTTAGTAGAGACGGGGTTTCTCCATGTTGGACAGGCTGGTCTTGAACTCTTGGCCT TTTTGTATTTTTAGTAGAGACGGGGTTTCTCCGTGTTGGACAGGCTGGTCTTGAACTCTTGGCCT T C LARS1 Ensembl:ENSG00000133706 Protein coding exon GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1437760810 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_265072,RMVar_hsa_circ_100747,RMVar_hsa_circ_235238,RMVar_hsa_circ_235236,RMVar_hsa_circ_104530,RMVar_hsa_circ_82362,RMVar_hsa_circ_235241,RMVar_hsa_circ_45752,RMVar_hsa_circ_59644,RMVar_hsa_circ_93600,RMVar_hsa_circ_113570,RMVar_hsa_circ_235243,RMVar_hsa_circ_235244,RMVar_hsa_circ_123626,RMVar_hsa_circ_235245 51652 RMVar_ID_51652 Human_SNP_ID_255138605 A-to-I Human chr5 - 146146790 146146790 146146790 AGAATCGCTTGAACCTGGGAGGCAGAGGTTGCAGTGAGTCGAGACGGCGCCACCACACTCCAGTC AGAATCGCTTGAACCTGGGAGGCAGAGGTTGCGGTGAGTCGAGACGGCGCCACCACACTCCAGTC T C LARS1 Ensembl:ENSG00000133706 Protein coding intron GSE107867 ASD brains,cerebellum;ASD brains,Fragile X samples from NIH NeuroBioBank;ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1398294195 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15339379 RMVar_hsa_circ_265072,RMVar_hsa_circ_100747,RMVar_hsa_circ_235238,RMVar_hsa_circ_235236,RMVar_hsa_circ_104530,RMVar_hsa_circ_82362,RMVar_hsa_circ_235241,RMVar_hsa_circ_45752,RMVar_hsa_circ_59644,RMVar_hsa_circ_93600,RMVar_hsa_circ_113570,RMVar_hsa_circ_235243,RMVar_hsa_circ_235244,RMVar_hsa_circ_123626,RMVar_hsa_circ_235245 51653 RMVar_ID_51653 Human_SNP_ID_255144076 A-to-I Human chr5 - 146168521 146168521 146168521 GCTACCACACCCAGCTAATTTTTATATTTAGTAGAGACATCATGTTGGCCAGGCTGGTCTCGAAC GCTACCACACCCAGCTAATTTTTATATTTAGTGGAGACATCATGTTGGCCAGGCTGGTCTCGAAC T C LARS1 Ensembl:ENSG00000133706 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs765507254 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7400833,Human_RBP_ID_15339856,Human_RBP_ID_25868882 RMVar_hsa_circ_265072,RMVar_hsa_circ_100747,RMVar_hsa_circ_235236,RMVar_hsa_circ_45752,RMVar_hsa_circ_123626,RMVar_hsa_circ_235245,RMVar_hsa_circ_52850,RMVar_hsa_circ_19629,RMVar_hsa_circ_5318,RMVar_hsa_circ_235246,RMVar_hsa_circ_36119,RMVar_hsa_circ_113738,RMVar_hsa_circ_235251,RMVar_hsa_circ_321047,RMVar_hsa_circ_276318,RMVar_hsa_circ_235254,RMVar_hsa_circ_324107,RMVar_hsa_circ_235256,RMVar_hsa_circ_74803,RMVar_hsa_circ_235255,RMVar_hsa_circ_361066,RMVar_hsa_circ_274839,RMVar_hsa_circ_43830,RMVar_hsa_circ_343860,RMVar_hsa_circ_235257,RMVar_hsa_circ_307433,RMVar_hsa_circ_235258,RMVar_hsa_circ_235259 51654 RMVar_ID_51654 Human_SNP_ID_255144939 A-to-I Human chr5 - 146171959 146171959 146171959 GTTTGCTGTAGGGTACCAGCGATTGAAAGGAAAATGTTGTCTGTTTCCCTTTGGCCTGCACTGTA GTTTGCTGTAGGGTACCAGCGATTGAAAGGAAGATGTTGTCTGTTTCCCTTTGGCCTGCACTGTA T C LARS1 Ensembl:ENSG00000133706 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs112954500 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_75327,Human_RBP_ID_214507,Human_RBP_ID_787903,Human_RBP_ID_943846,Human_RBP_ID_1647291,Human_RBP_ID_1989685,Human_RBP_ID_3968306,Human_RBP_ID_9262355,Human_RBP_ID_15339923,Human_RBP_ID_18835443,Human_RBP_ID_23051251,Human_RBP_ID_23214327,Human_RBP_ID_24089286,Human_RBP_ID_25868902 Human_Splice_Rec_704390,Human_Splice_Rec_704391,Human_Splice_Rec_704566,Human_Splice_Rec_704567,Human_Splice_Rec_704626,Human_Splice_Rec_704627,Human_Splice_Rec_704688,Human_Splice_Rec_704689,Human_Splice_Rec_704748,Human_Splice_Rec_704749,Human_Splice_Rec_704808,Human_Splice_Rec_704809,Human_Splice_Rec_704868,Human_Splice_Rec_704869,Human_Splice_Rec_704930,Human_Splice_Rec_704931,Human_Splice_Rec_704992,Human_Splice_Rec_704993,Human_Splice_Rec_705054,Human_Splice_Rec_705055,Human_Splice_Rec_705116,Human_Splice_Rec_705117,Human_Splice_Rec_705178,Human_Splice_Rec_705179,Human_Splice_Rec_705240,Human_Splice_Rec_705241,Human_Splice_Rec_705300,Human_Splice_Rec_705301,Human_Splice_Rec_705362,Human_Splice_Rec_705363,Human_Splice_Rec_705434,Human_Splice_Rec_705435,Human_Splice_Rec_705500,Human_Splice_Rec_705501,Human_Splice_Rec_705528,Human_Splice_Rec_705529,Human_Splice_Rec_705556,Human_Splice_Rec_705557,Human_Splice_Rec_705582,Human_Splice_Rec_705583,Human_Splice_Rec_705608,Human_Splice_Rec_705609,Human_Splice_Rec_705624,Human_Splice_Rec_705625 Clinvar_Rec_142 RMVar_hsa_circ_265072,RMVar_hsa_circ_100747,RMVar_hsa_circ_235236,RMVar_hsa_circ_45752,RMVar_hsa_circ_123626,RMVar_hsa_circ_235245,RMVar_hsa_circ_52850,RMVar_hsa_circ_19629,RMVar_hsa_circ_5318,RMVar_hsa_circ_235246,RMVar_hsa_circ_36119,RMVar_hsa_circ_113738,RMVar_hsa_circ_235251,RMVar_hsa_circ_321047,RMVar_hsa_circ_276318,RMVar_hsa_circ_235254,RMVar_hsa_circ_324107,RMVar_hsa_circ_235256,RMVar_hsa_circ_74803,RMVar_hsa_circ_235255,RMVar_hsa_circ_361066,RMVar_hsa_circ_274839,RMVar_hsa_circ_43830,RMVar_hsa_circ_343860,RMVar_hsa_circ_235257,RMVar_hsa_circ_307433,RMVar_hsa_circ_235258,RMVar_hsa_circ_235259,RMVar_hsa_circ_298505,RMVar_hsa_circ_337072 51655 RMVar_ID_51655 Human_SNP_ID_255147263 A-to-I Human chr5 - 146179084 146179084 146179084 GAGATTATAGGCGCATGCCAACGCATCCGGCTAATTTTTGTATTTTTAGTAGAAATGGGGTTTCG GAGATTATAGGCGCATGCCAACGCATCCGGCTCATTTTTGTATTTTTAGTAGAAATGGGGTTTCG T G LARS1 Ensembl:ENSG00000133706 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1470967329 Functional Loss SNV dbSNP153 33..33 33 - - - 51656 RMVar_ID_51656 Human_SNP_ID_255147875 A-to-I Human chr5 - 146181506 146181506 146181506 GGTACTGCAAGCGTGCTCCATTACACCCTGCTAATTTTTTGTATTTTTAGTAGAGACAGGGTTTC GGTACTGCAAGCGTGCTCCATTACACCCTGCTGATTTTTTGTATTTTTAGTAGAGACAGGGTTTC T C LARS1 Ensembl:ENSG00000133706 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1049066911 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15340147 51657 RMVar_ID_51657 Human_SNP_ID_255147876 A-to-I Human chr5 - 146181506 146181506 146181506 GGTACTGCAAGCGTGCTCCATTACACCCTGCTAATTTTTTGTATTTTTAGTAGAGACAGGGTTTC GGTACTGCAAGCGTGCTCCATTACACCCTGCTCATTTTTTGTATTTTTAGTAGAGACAGGGTTTC T G LARS1 Ensembl:ENSG00000133706 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1049066911 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15340147 51658 RMVar_ID_51658 Human_SNP_ID_255156769 A-to-I Human chr5 + 146212779 146212779 146212779 TTGCCCAGGCTGGAGTGCAGTGGCGTGATCTCAGTTCACTGCAACCTCCGTCTCCTGGATGGATT TTGCCCAGGCTGGAGTGCAGTGGCGTGATCTCGGTTCACTGCAACCTCCGTCTCCTGGATGGATT A G RBM27,AC091959.3 Ensembl:ENSG00000091009,Ensembl:ENSG00000275740 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232757260 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_121108,RMVar_hsa_circ_235260 51659 RMVar_ID_51659 Human_SNP_ID_255163301 A-to-I Human chr5 + 146238393 146238393 146238393 AGCTGGGCGTTGTGGAGCATGCCTGTAGTCCCAGCAACTCGGGAGGCTGAGGCAGGAGAATCACT AGCTGGGCGTTGTGGAGCATGCCTGTAGTCCCCGCAACTCGGGAGGCTGAGGCAGGAGAATCACT A C RBM27,AC091959.3 Ensembl:ENSG00000091009,Ensembl:ENSG00000275740 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs530487841 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_235262,RMVar_hsa_circ_121973,RMVar_hsa_circ_378480,RMVar_hsa_circ_92449,RMVar_hsa_circ_235261,RMVar_hsa_circ_329863,RMVar_hsa_circ_87947,RMVar_hsa_circ_10909,RMVar_hsa_circ_63852,RMVar_hsa_circ_112549,RMVar_hsa_circ_235268,RMVar_hsa_circ_235269,RMVar_hsa_circ_86968,RMVar_hsa_circ_235272,RMVar_hsa_circ_235273,RMVar_hsa_circ_43841,RMVar_hsa_circ_309022,RMVar_hsa_circ_24805,RMVar_hsa_circ_20558,RMVar_hsa_circ_266989,RMVar_hsa_circ_235278,RMVar_hsa_circ_5297,RMVar_hsa_circ_235277,RMVar_hsa_circ_372315,RMVar_hsa_circ_267781,RMVar_hsa_circ_99284,RMVar_hsa_circ_100748,RMVar_hsa_circ_81452,RMVar_hsa_circ_235280,RMVar_hsa_circ_235282,RMVar_hsa_circ_235283,RMVar_hsa_circ_235281 51660 RMVar_ID_51660 Human_SNP_ID_255163892 A-to-I Human chr5 + 146240456 146240456 146240456 TCAAGTGATTCTTGTGCCTCAGCTTCCCAAGTAGCTGGGATTACAGTCGCCCACCACCACACCTG TCAAGTGATTCTTGTGCCTCAGCTTCCCAAGTGGCTGGGATTACAGTCGCCCACCACCACACCTG A G RBM27,AC091959.3 Ensembl:ENSG00000091009,Ensembl:ENSG00000275740 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs988644015 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_235262,RMVar_hsa_circ_121973,RMVar_hsa_circ_378480,RMVar_hsa_circ_92449,RMVar_hsa_circ_235261,RMVar_hsa_circ_329863,RMVar_hsa_circ_87947,RMVar_hsa_circ_10909,RMVar_hsa_circ_63852,RMVar_hsa_circ_112549,RMVar_hsa_circ_235268,RMVar_hsa_circ_235269,RMVar_hsa_circ_86968,RMVar_hsa_circ_235272,RMVar_hsa_circ_235273,RMVar_hsa_circ_43841,RMVar_hsa_circ_309022,RMVar_hsa_circ_24805,RMVar_hsa_circ_20558,RMVar_hsa_circ_266989,RMVar_hsa_circ_235278,RMVar_hsa_circ_5297,RMVar_hsa_circ_235277,RMVar_hsa_circ_372315,RMVar_hsa_circ_267781,RMVar_hsa_circ_99284,RMVar_hsa_circ_100748,RMVar_hsa_circ_81452,RMVar_hsa_circ_235280,RMVar_hsa_circ_235282,RMVar_hsa_circ_235283,RMVar_hsa_circ_235281 51661 RMVar_ID_51661 Human_SNP_ID_255164450 A-to-I Human chr5 + 146242778 146242778 146242778 ACCAAGCCCGGCTAATTTTTTTTTGTATTTTTAGTAAAGACAGGGTTTCACCATGTTGGCCAGGC ACCAAGCCCGGCTAATTTTTTTTTGTATTTTTCGTAAAGACAGGGTTTCACCATGTTGGCCAGGC A C RBM27,AC091959.3 Ensembl:ENSG00000091009,Ensembl:ENSG00000275740 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs78191081 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_235262,RMVar_hsa_circ_121973,RMVar_hsa_circ_378480,RMVar_hsa_circ_92449,RMVar_hsa_circ_235261,RMVar_hsa_circ_329863,RMVar_hsa_circ_87947,RMVar_hsa_circ_10909,RMVar_hsa_circ_63852,RMVar_hsa_circ_112549,RMVar_hsa_circ_235268,RMVar_hsa_circ_235269,RMVar_hsa_circ_86968,RMVar_hsa_circ_235272,RMVar_hsa_circ_235273,RMVar_hsa_circ_43841,RMVar_hsa_circ_309022,RMVar_hsa_circ_24805,RMVar_hsa_circ_20558,RMVar_hsa_circ_266989,RMVar_hsa_circ_235278,RMVar_hsa_circ_5297,RMVar_hsa_circ_235277,RMVar_hsa_circ_372315,RMVar_hsa_circ_267781,RMVar_hsa_circ_99284,RMVar_hsa_circ_100748,RMVar_hsa_circ_81452,RMVar_hsa_circ_235280,RMVar_hsa_circ_235282,RMVar_hsa_circ_235283,RMVar_hsa_circ_235281 51662 RMVar_ID_51662 Human_SNP_ID_255165804 A-to-I Human chr5 + 146248646 146248646 146248646 CACCACTACGCCTGGCTAATTTTTGTAATTTTAGTAGAGACGGGGTTTCACCCTATTGCCCAGCC CACCACTACGCCTGGCTAATTTTTGTAATTTTGGTAGAGACGGGGTTTCACCCTATTGCCCAGCC A G RBM27,AC091959.3 Ensembl:ENSG00000091009,Ensembl:ENSG00000275740 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1434856452 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15340937 RMVar_hsa_circ_235262,RMVar_hsa_circ_121973,RMVar_hsa_circ_378480,RMVar_hsa_circ_92449,RMVar_hsa_circ_235261,RMVar_hsa_circ_329863,RMVar_hsa_circ_87947,RMVar_hsa_circ_10909,RMVar_hsa_circ_63852,RMVar_hsa_circ_112549,RMVar_hsa_circ_235268,RMVar_hsa_circ_235269,RMVar_hsa_circ_86968,RMVar_hsa_circ_235272,RMVar_hsa_circ_235273,RMVar_hsa_circ_43841,RMVar_hsa_circ_309022,RMVar_hsa_circ_24805,RMVar_hsa_circ_20558,RMVar_hsa_circ_266989,RMVar_hsa_circ_235278,RMVar_hsa_circ_5297,RMVar_hsa_circ_235277,RMVar_hsa_circ_372315,RMVar_hsa_circ_267781,RMVar_hsa_circ_99284,RMVar_hsa_circ_100748,RMVar_hsa_circ_81452,RMVar_hsa_circ_235280,RMVar_hsa_circ_235282,RMVar_hsa_circ_235283,RMVar_hsa_circ_235281 51663 RMVar_ID_51663 Human_SNP_ID_255165811 A-to-I Human chr5 + 146248668 146248668 146248668 TTGTAATTTTAGTAGAGACGGGGTTTCACCCTATTGCCCAGCCTGGTCTCAAATTCCTGAGCTCA TTGTAATTTTAGTAGAGACGGGGTTTCACCCTCTTGCCCAGCCTGGTCTCAAATTCCTGAGCTCA A C RBM27,AC091959.3 Ensembl:ENSG00000091009,Ensembl:ENSG00000275740 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs113022299 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15340937 RMVar_hsa_circ_235262,RMVar_hsa_circ_121973,RMVar_hsa_circ_378480,RMVar_hsa_circ_92449,RMVar_hsa_circ_235261,RMVar_hsa_circ_329863,RMVar_hsa_circ_87947,RMVar_hsa_circ_10909,RMVar_hsa_circ_63852,RMVar_hsa_circ_112549,RMVar_hsa_circ_235268,RMVar_hsa_circ_235269,RMVar_hsa_circ_86968,RMVar_hsa_circ_235272,RMVar_hsa_circ_235273,RMVar_hsa_circ_43841,RMVar_hsa_circ_309022,RMVar_hsa_circ_24805,RMVar_hsa_circ_20558,RMVar_hsa_circ_266989,RMVar_hsa_circ_235278,RMVar_hsa_circ_5297,RMVar_hsa_circ_235277,RMVar_hsa_circ_372315,RMVar_hsa_circ_267781,RMVar_hsa_circ_99284,RMVar_hsa_circ_100748,RMVar_hsa_circ_81452,RMVar_hsa_circ_235280,RMVar_hsa_circ_235282,RMVar_hsa_circ_235283,RMVar_hsa_circ_235281 51664 RMVar_ID_51664 Human_SNP_ID_255165812 A-to-I Human chr5 + 146248668 146248668 146248668 TTGTAATTTTAGTAGAGACGGGGTTTCACCCTATTGCCCAGCCTGGTCTCAAATTCCTGAGCTCA TTGTAATTTTAGTAGAGACGGGGTTTCACCCTGTTGCCCAGCCTGGTCTCAAATTCCTGAGCTCA A G RBM27,AC091959.3 Ensembl:ENSG00000091009,Ensembl:ENSG00000275740 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs113022299 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15340937 RMVar_hsa_circ_235262,RMVar_hsa_circ_121973,RMVar_hsa_circ_378480,RMVar_hsa_circ_92449,RMVar_hsa_circ_235261,RMVar_hsa_circ_329863,RMVar_hsa_circ_87947,RMVar_hsa_circ_10909,RMVar_hsa_circ_63852,RMVar_hsa_circ_112549,RMVar_hsa_circ_235268,RMVar_hsa_circ_235269,RMVar_hsa_circ_86968,RMVar_hsa_circ_235272,RMVar_hsa_circ_235273,RMVar_hsa_circ_43841,RMVar_hsa_circ_309022,RMVar_hsa_circ_24805,RMVar_hsa_circ_20558,RMVar_hsa_circ_266989,RMVar_hsa_circ_235278,RMVar_hsa_circ_5297,RMVar_hsa_circ_235277,RMVar_hsa_circ_372315,RMVar_hsa_circ_267781,RMVar_hsa_circ_99284,RMVar_hsa_circ_100748,RMVar_hsa_circ_81452,RMVar_hsa_circ_235280,RMVar_hsa_circ_235282,RMVar_hsa_circ_235283,RMVar_hsa_circ_235281 51665 RMVar_ID_51665 Human_SNP_ID_255165944 A-to-I Human chr5 + 146249188 146249188 146249188 AATATTTAGTAGAGACAGAGTCTCGGTATGTTACTCAGGCTGGTCTCAAACTCCTGAGCTCAAGT AATATTTAGTAGAGACAGAGTCTCGGTATGTTGCTCAGGCTGGTCTCAAACTCCTGAGCTCAAGT A G RBM27,AC091959.3 Ensembl:ENSG00000091009,Ensembl:ENSG00000275740 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1407414496 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_235262,RMVar_hsa_circ_121973,RMVar_hsa_circ_378480,RMVar_hsa_circ_92449,RMVar_hsa_circ_235261,RMVar_hsa_circ_329863,RMVar_hsa_circ_87947,RMVar_hsa_circ_10909,RMVar_hsa_circ_63852,RMVar_hsa_circ_112549,RMVar_hsa_circ_235268,RMVar_hsa_circ_235269,RMVar_hsa_circ_86968,RMVar_hsa_circ_235272,RMVar_hsa_circ_235273,RMVar_hsa_circ_43841,RMVar_hsa_circ_309022,RMVar_hsa_circ_24805,RMVar_hsa_circ_20558,RMVar_hsa_circ_266989,RMVar_hsa_circ_235278,RMVar_hsa_circ_5297,RMVar_hsa_circ_235277,RMVar_hsa_circ_372315,RMVar_hsa_circ_267781,RMVar_hsa_circ_99284,RMVar_hsa_circ_100748,RMVar_hsa_circ_81452,RMVar_hsa_circ_235280,RMVar_hsa_circ_235282,RMVar_hsa_circ_235283,RMVar_hsa_circ_235281 51666 RMVar_ID_51666 Human_SNP_ID_255173559 A-to-I Human chr5 + 146279697 146279697 146279697 AGCTGTGGTGGCATCTGCCTGTAGTCGCAGCTACTCGGGAGCCTGAGGCACATGAATTGCTTGAG AGCTGTGGTGGCATCTGCCTGTAGTCGCAGCTGCTCGGGAGCCTGAGGCACATGAATTGCTTGAG A G RBM27,AC091959.3 Ensembl:ENSG00000091009,Ensembl:ENSG00000275740 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025143888 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15341289 RMVar_hsa_circ_121973,RMVar_hsa_circ_235261,RMVar_hsa_circ_267781,RMVar_hsa_circ_1683,RMVar_hsa_circ_107671,RMVar_hsa_circ_235299 51667 RMVar_ID_51667 Human_SNP_ID_255175719 A-to-I Human chr5 + 146288939 146288939 146288939 GTGAAAAGGAATAGTGGTTCCTCTTGATGTATAGTATGCCTGTATTATAGTTTTTACAAAATTGT GTGAAAAGGAATAGTGGTTCCTCTTGATGTATGGTATGCCTGTATTATAGTTTTTACAAAATTGT A G RBM27,AC091959.3 Ensembl:ENSG00000091009,Ensembl:ENSG00000275740 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs758134635 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_12518,Human_RBP_ID_1390537,Human_RBP_ID_8950942,Human_RBP_ID_21900781,Human_RBP_ID_24089411,Human_RBP_ID_26529396 Human_miRNA_ID_2507520,Human_miRNA_ID_2526507,Human_miRNA_ID_2529681,Human_miRNA_ID_2532095,Human_miRNA_ID_2983185 RMVar_hsa_circ_121973,RMVar_hsa_circ_235261,RMVar_hsa_circ_267781,RMVar_hsa_circ_107671,RMVar_hsa_circ_235299 51668 RMVar_ID_51668 Human_SNP_ID_255216497 A-to-I Human chr5 + 146453940 146453940 146453940 TTCCTTCCGGCCAGGCGCTGTGGCTCATGCCTATAATCCTAGCACTTTGGGAGGCCGAGGAGGGC TTCCTTCCGGCCAGGCGCTGTGGCTCATGCCTGTAATCCTAGCACTTTGGGAGGCCGAGGAGGGC A G TCERG1 Ensembl:ENSG00000113649 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1296972184 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_102557,RMVar_hsa_circ_125761,RMVar_hsa_circ_235301,RMVar_hsa_circ_101453,RMVar_hsa_circ_235302,RMVar_hsa_circ_235300 51669 RMVar_ID_51669 Human_SNP_ID_255217792 A-to-I Human chr5 + 146459050 146458997 146459051 TCAGGCCCAGGCGCAGGCTCAGGCCCAGGCACAAGCTCAGGCCCAGGCTCAGGCTCAGGCCCAGG __________________________________GCTCAGGCCCAGGCTCAGGCTCAGGCCCAGG GGCTCAGGCCCAGGCGCAGGCTCAGGCCCAGGCGCAGGCTCAGGCCCAGGCACAA G TCERG1 Ensembl:ENSG00000113649 Protein coding exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1561638521 Functional Loss DEL dbSNP153 1..34 33 - - - Human_RBP_ID_26764015 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 51670 RMVar_ID_51670 Human_SNP_ID_255217808 A-to-I Human chr5 + 146459050 146459015 146459051 TCAGGCCCAGGCGCAGGCTCAGGCCCAGGCACAAGCTCAGGCCCAGGCTCAGGCTCAGGCCCAGG __________________________________GCTCAGGCCCAGGCTCAGGCTCAGGCCCAGG GGCTCAGGCCCAGGCGCAGGCTCAGGCCCAGGCACAA G TCERG1 Ensembl:ENSG00000113649 Protein coding exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs772057166 Functional Loss DEL dbSNP153 1..34 33 - - - Human_RBP_ID_26764015 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 51671 RMVar_ID_51671 Human_SNP_ID_255217827 A-to-I Human chr5 + 146459050 146459033 146459051 TCAGGCCCAGGCGCAGGCTCAGGCCCAGGCACAAGCTCAGGCCCAGGCTCAGGCTCAGGCCCAGG TCAGGCCCAGGCGCAG__________________GCTCAGGCCCAGGCTCAGGCTCAGGCCCAGG GGCTCAGGCCCAGGCACAA G TCERG1 Ensembl:ENSG00000113649 Protein coding exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs759866842 Functional Loss DEL dbSNP153 17..34 33 - - - Human_RBP_ID_26764015 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 51672 RMVar_ID_51672 Human_SNP_ID_255217837 A-to-I Human chr5 + 146459050 146459045 146459051 TCAGGCCCAGGCGCAGGCTCAGGCCCAGGCACAAGCTCAGGCCCAGGCTCAGGCTCAGGCCCAGG TCAGGCCCAGGCGCAGGCTCAGGCCCAG______GCTCAGGCCCAGGCTCAGGCTCAGGCCCAGG GGCACAA G TCERG1 Ensembl:ENSG00000113649 Protein coding exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs775964149 Functional Loss DEL dbSNP153 29..34 33 - - - Human_RBP_ID_26764015 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 51673 RMVar_ID_51673 Human_SNP_ID_255217838 A-to-I Human chr5 + 146459050 146459047 146459051 TCAGGCCCAGGCGCAGGCTCAGGCCCAGGCACAAGCTCAGGCCCAGGCTCAGGCTCAGGCCCAGG TCAGGCCCAGGCGCAGGCTCAGGCCCAGGC____GCTCAGGCCCAGGCTCAGGCTCAGGCCCAGG CACAA C TCERG1 Ensembl:ENSG00000113649 Protein coding exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs763393898 Functional Loss DEL dbSNP153 31..34 33 - - - Human_RBP_ID_26764015 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 51674 RMVar_ID_51674 Human_SNP_ID_255227133 A-to-I Human chr5 + 146497248 146497248 146497248 AGGCTGGAGTGCAGTGGCACGATCTCGGCTCTACAGCCTTTGCCTCCCAGGTTCAAAAGATTATT AGGCTGGAGTGCAGTGGCACGATCTCGGCTCTGCAGCCTTTGCCTCCCAGGTTCAAAAGATTATT A G TCERG1 Ensembl:ENSG00000113649 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs911714541 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7402233,Human_RBP_ID_15343195 RMVar_hsa_circ_101453,RMVar_hsa_circ_235300,RMVar_hsa_circ_119316,RMVar_hsa_circ_126626,RMVar_hsa_circ_115636,RMVar_hsa_circ_235307,RMVar_hsa_circ_235308,RMVar_hsa_circ_235309,RMVar_hsa_circ_52492,RMVar_hsa_circ_305646,RMVar_hsa_circ_9257,RMVar_hsa_circ_50198,RMVar_hsa_circ_280431,RMVar_hsa_circ_323238,RMVar_hsa_circ_359689,RMVar_hsa_circ_55385,RMVar_hsa_circ_100678,RMVar_hsa_circ_54300,RMVar_hsa_circ_82659,RMVar_hsa_circ_235316,RMVar_hsa_circ_235317,RMVar_hsa_circ_353582,RMVar_hsa_circ_235315,RMVar_hsa_circ_306439,RMVar_hsa_circ_45791,RMVar_hsa_circ_235318,RMVar_hsa_circ_235319 51675 RMVar_ID_51675 Human_SNP_ID_255227146 A-to-I Human chr5 + 146497300 146497300 146497300 TCAAAAGATTATTTTGCCTCAGCTTCTCAAGTAGCTGGGATTACAGGCGTCAGCTACTGTGCCTG TCAAAAGATTATTTTGCCTCAGCTTCTCAAGTTGCTGGGATTACAGGCGTCAGCTACTGTGCCTG A T TCERG1 Ensembl:ENSG00000113649 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1374490022 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15343200 RMVar_hsa_circ_101453,RMVar_hsa_circ_235300,RMVar_hsa_circ_119316,RMVar_hsa_circ_126626,RMVar_hsa_circ_115636,RMVar_hsa_circ_235307,RMVar_hsa_circ_235308,RMVar_hsa_circ_235309,RMVar_hsa_circ_52492,RMVar_hsa_circ_305646,RMVar_hsa_circ_9257,RMVar_hsa_circ_50198,RMVar_hsa_circ_280431,RMVar_hsa_circ_323238,RMVar_hsa_circ_359689,RMVar_hsa_circ_55385,RMVar_hsa_circ_100678,RMVar_hsa_circ_54300,RMVar_hsa_circ_82659,RMVar_hsa_circ_235316,RMVar_hsa_circ_235317,RMVar_hsa_circ_353582,RMVar_hsa_circ_235315,RMVar_hsa_circ_306439,RMVar_hsa_circ_45791,RMVar_hsa_circ_235318,RMVar_hsa_circ_235319 51676 RMVar_ID_51676 Human_SNP_ID_255227164 A-to-I Human chr5 + 146497394 146497394 146497394 GTCTCGAACTCCTGGCCTCAAATGATCCTCCTACCTTGCCCTCCTGACGTGCTGGGATTGCATGC GTCTCGAACTCCTGGCCTCAAATGATCCTCCTGCCTTGCCCTCCTGACGTGCTGGGATTGCATGC A G TCERG1 Ensembl:ENSG00000113649 Protein coding intron GSE100210;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229 RNA-Seq:(High) rs1343811079 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10189891,Human_RBP_ID_15343200,Human_RBP_ID_26771559 RMVar_hsa_circ_101453,RMVar_hsa_circ_235300,RMVar_hsa_circ_119316,RMVar_hsa_circ_126626,RMVar_hsa_circ_115636,RMVar_hsa_circ_235307,RMVar_hsa_circ_235308,RMVar_hsa_circ_235309,RMVar_hsa_circ_52492,RMVar_hsa_circ_305646,RMVar_hsa_circ_9257,RMVar_hsa_circ_50198,RMVar_hsa_circ_280431,RMVar_hsa_circ_323238,RMVar_hsa_circ_359689,RMVar_hsa_circ_55385,RMVar_hsa_circ_100678,RMVar_hsa_circ_54300,RMVar_hsa_circ_82659,RMVar_hsa_circ_235316,RMVar_hsa_circ_235317,RMVar_hsa_circ_353582,RMVar_hsa_circ_235315,RMVar_hsa_circ_306439,RMVar_hsa_circ_45791,RMVar_hsa_circ_235318,RMVar_hsa_circ_235319 51677 RMVar_ID_51677 Human_SNP_ID_255303405 A-to-I Human chr5 - 146816153 146816153 146816153 GCGAGCCTCCTGCCTCAGCATCCAAAAGTGCTAGGATTACAGGCATGAGCCCACTATTATTAATA GCGAGCCTCCTGCCTCAGCATCCAAAAGTGCTCGGATTACAGGCATGAGCCCACTATTATTAATA T G PPP2R2B Ensembl:ENSG00000156475 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1024594589 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27564,RMVar_hsa_circ_294502,RMVar_hsa_circ_376514 51678 RMVar_ID_51678 Human_SNP_ID_255306932 A-to-I Human chr5 - 146830680 146830680 146830680 ATCACTTGAGGTCAGGAGCTCAAGACCAGCCTAGCCAACATGGTGAATCCCATCTGTACTAAAAA ATCACTTGAGGTCAGGAGCTCAAGACCAGCCTTGCCAACATGGTGAATCCCATCTGTACTAAAAA T A PPP2R2B Ensembl:ENSG00000156475 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs946347729 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27564,RMVar_hsa_circ_294502,RMVar_hsa_circ_376514 51679 RMVar_ID_51679 Human_SNP_ID_255309952 A-to-I Human chr5 - 146842702 146842702 146842702 TGTTCTCACTTATAAGTGGGAGCTAAATGATGAGAACACACGGATACATAGAGAGGAACAACACA TGTTCTCACTTATAAGTGGGAGCTAAATGATGGGAACACACGGATACATAGAGAGGAACAACACA T C PPP2R2B Ensembl:ENSG00000156475 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1041593528 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27564,RMVar_hsa_circ_294502,RMVar_hsa_circ_376514 51680 RMVar_ID_51680 Human_SNP_ID_255309958 A-to-I Human chr5 - 146842721 146842721 146842721 CAGAAAACCAAATATGGCATGTTCTCACTTATAAGTGGGAGCTAAATGATGAGAACACACGGATA CAGAAAACCAAATATGGCATGTTCTCACTTATTAGTGGGAGCTAAATGATGAGAACACACGGATA T A PPP2R2B Ensembl:ENSG00000156475 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1002576294 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27564,RMVar_hsa_circ_294502,RMVar_hsa_circ_376514 51681 RMVar_ID_51681 Human_SNP_ID_255310710 A-to-I Human chr5 - 146845410 146845410 146845410 TCTCTACTAAAAGTGCAAAAAAAAATTTAGCCAGGCATGAACCTGGGAGGCGGAGCTTGCAGTGA TCTCTACTAAAAGTGCAAAAAAAAATTTAGCCGGGCATGAACCTGGGAGGCGGAGCTTGCAGTGA T C PPP2R2B Ensembl:ENSG00000156475 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1298664497 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27564,RMVar_hsa_circ_294502,RMVar_hsa_circ_376514 51682 RMVar_ID_51682 Human_SNP_ID_255322595 A-to-I Human chr5 - 146894564 146894564 146894564 GTGGTGGCGCACGCCTGTGGTCCCAGCTACTCAGGAGGCTGAGGTGGGAGGATTTCTTGAACCTA GTGGTGGCGCACGCCTGTGGTCCCAGCTACTCGGGAGGCTGAGGTGGGAGGATTTCTTGAACCTA T C PPP2R2B Ensembl:ENSG00000156475 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1307433093 Functional Loss SNV dbSNP153 33..33 33 - - - 51683 RMVar_ID_51683 Human_SNP_ID_255333645 A-to-I Human chr5 - 146938948 146938948 146938948 GGTGAAACCCTGTCTCTACTAAAATACAAAAAATTAGCCAGGTGTGGCAGCATGCGCCTGTAGTC GGTGAAACCCTGTCTCTACTAAAATACAAAAACTTAGCCAGGTGTGGCAGCATGCGCCTGTAGTC T G PPP2R2B Ensembl:ENSG00000156475 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs528701531 Functional Loss SNV dbSNP153 33..33 33 - - - 51684 RMVar_ID_51684 Human_SNP_ID_255335631 A-to-I Human chr5 - 146947832 146947832 146947832 GGCATTCCTAATGAAGTGGTAGCATAAGCAAAAGCATGGACTCATGAGAACACAGGGTTGCATGG GGCATTCCTAATGAAGTGGTAGCATAAGCAAAGGCATGGACTCATGAGAACACAGGGTTGCATGG T C PPP2R2B Ensembl:ENSG00000156475 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1191612945 Functional Loss SNV dbSNP153 33..33 33 - - - 51685 RMVar_ID_51685 Human_SNP_ID_255467661 A-to-I Human chr5 - 147489187 147489187 147489187 CAAAATAGGAAAGCAGAATCCGGTCAAGTCCAAAAGGTGAGCACAGTAGCTAAAGCAGAAAACAT CAAAATAGGAAAGCAGAATCCGGTCAAGTCCAGAAGGTGAGCACAGTAGCTAAAGCAGAAAACAT T C DPYSL3 Ensembl:ENSG00000113657 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1048795646 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99040,RMVar_hsa_circ_235346 51686 RMVar_ID_51686 Human_SNP_ID_255535220 A-to-I Human chr5 - 147770342 147770342 147770342 CAGAAATTGTGTTTGTCTATGTAAACCCATTTAGAACCTCTGACCCAGGTGGAGCAATTTTTCAG CAGAAATTGTGTTTGTCTATGTAAACCCATTTGGAACCTCTGACCCAGGTGGAGCAATTTTTCAG T C JAKMIP2 Ensembl:ENSG00000176049 Protein coding intron GSE107867 ASD brains,cerebellum;ASD brains,Fragile X samples from NIH NeuroBioBank - 30559470 RNA-Seq:(High) rs1248729959 Functional Loss SNV dbSNP153 33..33 33 - - - 51687 RMVar_ID_51687 Human_SNP_ID_255557725 A-to-I Human chr5 - 147864889 147864889 147864889 TCTGTAGAAAAGGAAGATTAGAAAGACTCAGCAACGCTTGGGATGGTACTGAGGGGACAGGCGGG TCTGTAGAAAAGGAAGATTAGAAAGACTCAGCGACGCTTGGGATGGTACTGAGGGGACAGGCGGG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs750470532 Functional Loss SNV dbSNP153 33..33 33 - - - 51688 RMVar_ID_51688 Human_SNP_ID_255686902 A-to-I Human chr5 + 148387747 148387747 148387747 TGGAGTCTAGCTCTGTTACCAGGCTCGAGTGCAGTCGTACGATCTTGGCTCACTGCAACCTCTGA TGGAGTCTAGCTCTGTTACCAGGCTCGAGTGCGGTCGTACGATCTTGGCTCACTGCAACCTCTGA A G FBXO38 Ensembl:ENSG00000145868 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1168832527 Functional Loss SNV dbSNP153 33..33 33 - - - 51689 RMVar_ID_51689 Human_SNP_ID_255921065 A-to-I Human chr5 + 149361137 149361137 149361137 GACTGTTTAATGATTAGTGTCAGGTGAGGCACAGTGGCTAATGCCTGTAATTCCAGCACTTGGGG GACTGTTTAATGATTAGTGTCAGGTGAGGCACGGTGGCTAATGCCTGTAATTCCAGCACTTGGGG A G PCYOX1L Ensembl:ENSG00000145882 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924257491 Functional Loss SNV dbSNP153 33..33 33 - - - 51690 RMVar_ID_51690 Human_SNP_ID_255935914 A-to-I Human chr5 + 149419317 149419317 149419317 CCTCTAATCCCAGTGCTTCAGGAGGACAAGGCAGGAGGATCACTTGAAGCCAGGAGTTCACGACC CCTCTAATCCCAGTGCTTCAGGAGGACAAGGCGGGAGGATCACTTGAAGCCAGGAGTTCACGACC A G CARMN Ensembl:ENSG00000249669 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1297209929 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_19649 51691 RMVar_ID_51691 Human_SNP_ID_255938505 A-to-I Human chr5 + 149429398 149429398 149429398 ATAATCTCAGCTCACTGCAACCTCCTCCTCCCAGGGTCAAGCAATTCTCGTGCCTCAGCCTCCCA ATAATCTCAGCTCACTGCAACCTCCTCCTCCCGGGGTCAAGCAATTCTCGTGCCTCAGCCTCCCA A G CARMN Ensembl:ENSG00000249669 lincRNA intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1379897107 Functional Loss SNV dbSNP153 33..33 33 - - - 51692 RMVar_ID_51692 Human_SNP_ID_255939169 A-to-I Human chr5 + 149431949 149431949 149431949 GGCCGGGCGCGGTGGCTCACACCTGTAATCCCAACACTTTGGGAGGCCCAGGCGGGTGGATCACG GGCCGGGCGCGGTGGCTCACACCTGTAATCCCGACACTTTGGGAGGCCCAGGCGGGTGGATCACG A G CARMN Ensembl:ENSG00000249669 lincRNA exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1049907814 Functional Loss SNV dbSNP153 33..33 33 - - - 51693 RMVar_ID_51693 Human_SNP_ID_255947964 A-to-I Human chr5 - 149467292 149467292 149467292 GCTGGAGTGCAATGGTGCGATCTCTGCTCACCACAACCTCCAGCTCCTGGATTCAAGCAATTCTC GCTGGAGTGCAATGGTGCGATCTCTGCTCACCGCAACCTCCAGCTCCTGGATTCAAGCAATTCTC T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1008404741 Functional Loss SNV dbSNP153 33..33 33 - - - 51694 RMVar_ID_51694 Human_SNP_ID_255954782 A-to-I Human chr5 - 149495026 149495026 149495026 GTATTTGTTTCTTGACTAATAAACCCTTTGATACTTTTAGCCAGAAATCAGTCTCATAAAGCTAT GTATTTGTTTCTTGACTAATAAACCCTTTGATGCTTTTAGCCAGAAATCAGTCTCATAAAGCTAT T C CSNK1A1,AC021078.1 Ensembl:ENSG00000113712,Ensembl:ENSG00000230551 Protein coding,lincRNA 3'UTR,exon GSE112787 293 Flip-In T-REx cells,empty vector - 29967493 RNA-Seq:(High) rs1033406824 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_634872,Human_RBP_ID_3762530,Human_RBP_ID_5215762,Human_RBP_ID_7404157,Human_RBP_ID_8213689,Human_RBP_ID_8886314,Human_RBP_ID_15347350,Human_RBP_ID_17412299,Human_RBP_ID_17528217,Human_RBP_ID_18042012,Human_RBP_ID_18355110,Human_RBP_ID_21137309,Human_RBP_ID_25871597,Human_RBP_ID_27736724 51695 RMVar_ID_51695 Human_SNP_ID_255957031 A-to-I Human chr5 - 149503793 149503793 149503793 TTTACTTCAGGCATTCAGCAGATTTCAGAAAGAATTACCTTATTTTAAGTTAGTTTCTTTGTTAG TTTACTTCAGGCATTCAGCAGATTTCAGAAAGGATTACCTTATTTTAAGTTAGTTTCTTTGTTAG T C CSNK1A1,AC021078.1 Ensembl:ENSG00000113712,Ensembl:ENSG00000230551 Protein coding,lincRNA intron,exon GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1011417093 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3762581,Human_RBP_ID_10235628,Human_RBP_ID_15347744,Human_RBP_ID_25938640 RMVar_hsa_circ_350146,RMVar_hsa_circ_235396 51696 RMVar_ID_51696 Human_SNP_ID_255963249 A-to-I Human chr5 - 149532010 149532010 149532010 GCCAGGAGTGGTCGCATATGCCTGTAATCCCAACAGGTGGATGAGGCATGAGAATCTCTTGAACC GCCAGGAGTGGTCGCATATGCCTGTAATCCCAGCAGGTGGATGAGGCATGAGAATCTCTTGAACC T C CSNK1A1 Ensembl:ENSG00000113712 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs914696673 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_310903,RMVar_hsa_circ_265447,RMVar_hsa_circ_235404 51697 RMVar_ID_51697 Human_SNP_ID_255963778 A-to-I Human chr5 - 149534401 149534401 149534401 CAGCTCACTGCAACCCCCGCCTCCCGGGTTCAAGCAATTCTTCTGCCTCAGCCTCCCGAGAGTAG CAGCTCACTGCAACCCCCGCCTCCCGGGTTCATGCAATTCTTCTGCCTCAGCCTCCCGAGAGTAG T A CSNK1A1 Ensembl:ENSG00000113712 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1370130147 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_310903,RMVar_hsa_circ_265447 51698 RMVar_ID_51698 Human_SNP_ID_255964274 A-to-I Human chr5 - 149536039 149536039 149536039 TGAGGCAGGAGAATCACTTGAACCCAGAAGGCAGAGATTGTGGTGAGCTGAGATCATGCCATTGT TGAGGCAGGAGAATCACTTGAACCCAGAAGGCGGAGATTGTGGTGAGCTGAGATCATGCCATTGT T C CSNK1A1 Ensembl:ENSG00000113712 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs999523063 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15348672 RMVar_hsa_circ_310903,RMVar_hsa_circ_265447 51699 RMVar_ID_51699 Human_SNP_ID_255964299 A-to-I Human chr5 - 149536118 149536117 149536118 AGAAACCCCATATCTACTAAAAATACAAAATTAGTCAGGCGTGGTGGCGCGTGCCTGTGATACCA AGAAACCCCATATCTACTAAAAATACAAAATT_GTCAGGCGTGGTGGCGCGTGCCTGTGATACCA CT C CSNK1A1 Ensembl:ENSG00000113712 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs754159102 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_25872234 RMVar_hsa_circ_310903,RMVar_hsa_circ_265447 51700 RMVar_ID_51700 Human_SNP_ID_255965612 A-to-I Human chr5 - 149541404 149541404 149541404 CCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGCGGATCACTTGAAATCAGGAGTTTG CCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGGATCACTTGAAATCAGGAGTTTG T C CSNK1A1 Ensembl:ENSG00000113712 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs71586127 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15348783 RMVar_hsa_circ_310903,RMVar_hsa_circ_265447 51701 RMVar_ID_51701 Human_SNP_ID_255965737 A-to-I Human chr5 - 149541932 149541932 149541932 CAGTCTTTCTCTGTTGCCCAGGCTGGGATGCAATGGCGTGATCTTGACTCACTGCAACCTCCACT CAGTCTTTCTCTGTTGCCCAGGCTGGGATGCAGTGGCGTGATCTTGACTCACTGCAACCTCCACT T C CSNK1A1 Ensembl:ENSG00000113712 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1451013892 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_310903,RMVar_hsa_circ_265447 51702 RMVar_ID_51702 Human_SNP_ID_255966414 A-to-I Human chr5 - 149542984 149542984 149542984 TTGCTGGAAATTATTAATTTGTGGCCAGGCGCAGTGGTTCACACCTGTAATCCCAGCACTTTGGG TTGCTGGAAATTATTAATTTGTGGCCAGGCGCTGTGGTTCACACCTGTAATCCCAGCACTTTGGG T A CSNK1A1 Ensembl:ENSG00000113712 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs916196575 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_310903,RMVar_hsa_circ_265447 51703 RMVar_ID_51703 Human_SNP_ID_255966622 A-to-I Human chr5 - 149543830 149543830 149543830 GTGGCTATTCAGAAGTATGATAATAGCACACTACAGCCTCAAACTCCTGGACTCAAATGATCCTC GTGGCTATTCAGAAGTATGATAATAGCACACTGCAGCCTCAAACTCCTGGACTCAAATGATCCTC T C CSNK1A1 Ensembl:ENSG00000113712 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs955248630 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7404855,Human_RBP_ID_15348817 RMVar_hsa_circ_310903,RMVar_hsa_circ_265447 51704 RMVar_ID_51704 Human_SNP_ID_255967873 A-to-I Human chr5 - 149548332 149548332 149548332 CACCTCCTGACCTCAGGTGATCCACCTGCCTCAGCCTCCCAAAGTGCTGGGATTATAGGCGTGAG CACCTCCTGACCTCAGGTGATCCACCTGCCTCGGCCTCCCAAAGTGCTGGGATTATAGGCGTGAG T C CSNK1A1 Ensembl:ENSG00000113712 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1296962081 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_310903,RMVar_hsa_circ_265447 51705 RMVar_ID_51705 Human_SNP_ID_255967961 A-to-I Human chr5 - 149548616 149548616 149548616 CCTCAGGTGATCTGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGTGCC CCTCAGGTGATCTGCCTGCCTCGGCCTCCCAAGGTGCTGGGATTACAGGCATGAGCCACTGTGCC T C CSNK1A1 Ensembl:ENSG00000113712 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs150577586 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_310903,RMVar_hsa_circ_265447 51706 RMVar_ID_51706 Human_SNP_ID_255968011 A-to-I Human chr5 - 149548749 149548749 149548749 TGCCTCCCGGGTTCAAGTGATTCTCGTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCGCCCG TGCCTCCCGGGTTCAAGTGATTCTCGTGCCTCGGCCTCCTGAGTAGCTGGGATTACAGGCGCCCG T C CSNK1A1 Ensembl:ENSG00000113712 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1425154950 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_310903,RMVar_hsa_circ_265447 51707 RMVar_ID_51707 Human_SNP_ID_255968017 A-to-I Human chr5 - 149548766 149548766 149548766 TGGCTCACTGCAACCTCTGCCTCCCGGGTTCAAGTGATTCTCGTGCCTCAGCCTCCTGAGTAGCT TGGCTCACTGCAACCTCTGCCTCCCGGGTTCAGGTGATTCTCGTGCCTCAGCCTCCTGAGTAGCT T C CSNK1A1 Ensembl:ENSG00000113712 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs942137328 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_310903,RMVar_hsa_circ_265447 51708 RMVar_ID_51708 Human_SNP_ID_255968028 A-to-I Human chr5 - 149548805 149548805 149548805 CTTGTGGTCCAGGCTGGAGTGCAATGAATGGCACGATCTTGGCTCACTGCAACCTCTGCCTCCCG CTTGTGGTCCAGGCTGGAGTGCAATGAATGGCGCGATCTTGGCTCACTGCAACCTCTGCCTCCCG T C CSNK1A1 Ensembl:ENSG00000113712 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,31158229 RNA-Seq:(High) rs370751781 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_15348932,Human_RBP_ID_23313871 RMVar_hsa_circ_310903,RMVar_hsa_circ_265447 51709 RMVar_ID_51709 Human_SNP_ID_255972753 A-to-I Human chr5 + 149568227 149568227 149568227 ATTTGTTTATTTTGTAGAGACAGGGTTTCGCCATATTGCCTAGGTTGGTCTTGAACTCCTGTGCT ATTTGTTTATTTTGTAGAGACAGGGTTTCGCCGTATTGCCTAGGTTGGTCTTGAACTCCTGTGCT A G ARHGEF37 Ensembl:ENSG00000183111 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs759022554 Functional Loss SNV dbSNP153 33..33 33 - - - 51710 RMVar_ID_51710 Human_SNP_ID_255972754 A-to-I Human chr5 + 149568229 149568229 149568229 TTGTTTATTTTGTAGAGACAGGGTTTCGCCATATTGCCTAGGTTGGTCTTGAACTCCTGTGCTCA TTGTTTATTTTGTAGAGACAGGGTTTCGCCATGTTGCCTAGGTTGGTCTTGAACTCCTGTGCTCA A G ARHGEF37 Ensembl:ENSG00000183111 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs1422154662 Functional Loss SNV dbSNP153 33..33 33 - - - 51711 RMVar_ID_51711 Human_SNP_ID_256024182 A-to-I Human chr5 + 149770704 149770704 149770704 AAAAAAAAAAAATCTGCTGAGTGTGGTGGCACATGCCTGTAGTCCTAGCTACTTGGGAGGCTGAG AAAAAAAAAAAATCTGCTGAGTGTGGTGGCACGTGCCTGTAGTCCTAGCTACTTGGGAGGCTGAG A G PPARGC1B Ensembl:ENSG00000155846 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs896734495 Functional Loss SNV dbSNP153 33..33 33 - - - 51712 RMVar_ID_51712 Human_SNP_ID_256024183 A-to-I Human chr5 + 149770704 149770704 149770704 AAAAAAAAAAAATCTGCTGAGTGTGGTGGCACATGCCTGTAGTCCTAGCTACTTGGGAGGCTGAG AAAAAAAAAAAATCTGCTGAGTGTGGTGGCACTTGCCTGTAGTCCTAGCTACTTGGGAGGCTGAG A T PPARGC1B Ensembl:ENSG00000155846 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs896734495 Functional Loss SNV dbSNP153 33..33 33 - - - 51713 RMVar_ID_51713 Human_SNP_ID_256045795 A-to-I Human chr5 - 149858532 149858532 149858532 GACTTCAAGCAATCCTCCTGCCTCAGCCTCCCAAAGTGTTGGGATTACAGGCGTGAGCCACTGCA GACTTCAAGCAATCCTCCTGCCTCAGCCTCCCGAAGTGTTGGGATTACAGGCGTGAGCCACTGCA T C PDE6A Ensembl:ENSG00000132915 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1406448771 Functional Loss SNV dbSNP153 33..33 33 - - - 51714 RMVar_ID_51714 Human_SNP_ID_256064639 A-to-I Human chr5 - 149932504 149932504 149932504 CCAAATGCTAGCGTGATAATAATGCAAGTTCCAGAGAGGATTGTTGTAGCAGGAAATAATGAGGA CCAAATGCTAGCGTGATAATAATGCAAGTTCCGGAGAGGATTGTTGTAGCAGGAAATAATGAGGA T C PDE6A,MFFP2 Ensembl:ENSG00000132915,Ensembl:ENSG00000251583 Protein coding,Pseudogene intron,exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs75204652 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_25484 51715 RMVar_ID_51715 Human_SNP_ID_256077048 A-to-I Human chr5 + 149981847 149981847 149981847 TGAGAAGGTAGATAGAAGAATGTCTAGCCAATAGGTTAAAATTTCAAGTGTCCAACATTTCCCAG TGAGAAGGTAGATAGAAGAATGTCTAGCCAATTGGTTAAAATTTCAAGTGTCCAACATTTCCCAG A T SLC26A2 Ensembl:ENSG00000155850 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1411372287 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2891839 RMVar_hsa_circ_115757,RMVar_hsa_circ_124959,RMVar_hsa_circ_235412,RMVar_hsa_circ_110163,RMVar_hsa_circ_235413,RMVar_hsa_circ_235414 51716 RMVar_ID_51716 Human_SNP_ID_256077377 A-to-I Human chr5 + 149983689 149983689 149983689 GCTTCCCACTCCTGGGCTCAAGTTATCCTTCCATTTTGGCCTCCTGAGTAGCTAGACCATAGGTA GCTTCCCACTCCTGGGCTCAAGTTATCCTTCCCTTTTGGCCTCCTGAGTAGCTAGACCATAGGTA A C SLC26A2 Ensembl:ENSG00000155850 Protein coding 3'UTR GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs913526981 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_635046,Human_RBP_ID_15349790 Human_miRNA_ID_1660258,Human_miRNA_ID_2770090 RMVar_hsa_circ_115757,RMVar_hsa_circ_124959,RMVar_hsa_circ_235412,RMVar_hsa_circ_110163,RMVar_hsa_circ_235413,RMVar_hsa_circ_235414 51717 RMVar_ID_51717 Human_SNP_ID_256077387 A-to-I Human chr5 + 149983733 149983733 149983733 TGAGTAGCTAGACCATAGGTATGCATCACCACACCCTGCTAATTTTTTAAATTTTTTTCTAGAGA TGAGTAGCTAGACCATAGGTATGCATCACCACGCCCTGCTAATTTTTTAAATTTTTTTCTAGAGA A G SLC26A2 Ensembl:ENSG00000155850 Protein coding 3'UTR GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs558781341 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7405151,Human_RBP_ID_8886475 Human_miRNA_ID_1122261,Human_miRNA_ID_2528101 RMVar_hsa_circ_115757,RMVar_hsa_circ_124959,RMVar_hsa_circ_235412,RMVar_hsa_circ_110163,RMVar_hsa_circ_235413,RMVar_hsa_circ_235414 51718 RMVar_ID_51718 Human_SNP_ID_256077520 A-to-I Human chr5 + 149984404 149984404 149984404 GTTTTCGGCCAGGTGCAGTGGCTCATGCCTGTAATCCCAGCACGTTGGGAGGCCGAGGCGGGTGG GTTTTCGGCCAGGTGCAGTGGCTCATGCCTGTGATCCCAGCACGTTGGGAGGCCGAGGCGGGTGG A G SLC26A2 Ensembl:ENSG00000155850 Protein coding 3'UTR GSE47997;GSE38233;GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,24183664,29129909,31158229,31158229,31158229,31158229,31158229,31158229,32596459,32596459 RNA-Seq:(High) rs1284330315 Functional Loss SNV dbSNP153 33..33 33 - - - Human_miRNA_ID_2085527 RMVar_hsa_circ_115757,RMVar_hsa_circ_124959,RMVar_hsa_circ_235412,RMVar_hsa_circ_110163,RMVar_hsa_circ_235413,RMVar_hsa_circ_235414 51719 RMVar_ID_51719 Human_SNP_ID_376358277 A-to-I Human chr8 + 105453685 105453685 105453685 TCTTTTTGAAATGGAGTCTTGCCCTGTCATCCAGGCTGAAGTGCAGTGGCCCCATCTCAGCTCAC TCTTTTTGAAATGGAGTCTTGCCCTGTCATCCGGGCTGAAGTGCAGTGGCCCCATCTCAGCTCAC A G ZFPM2 Ensembl:ENSG00000169946 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1183523404 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86847,RMVar_hsa_circ_321766,RMVar_hsa_circ_307362,RMVar_hsa_circ_253833,RMVar_hsa_circ_253831,RMVar_hsa_circ_253832,RMVar_hsa_circ_336207,RMVar_hsa_circ_361480 51720 RMVar_ID_51720 Human_SNP_ID_376368042 A-to-I Human chr8 + 105496220 105496220 105496220 GAGGTGTAGGGGGAGTTCTCACTATGTTGTCCAGGCTGGGTCTTGAATTCCTGAGCTCAAGCAAT GAGGTGTAGGGGGAGTTCTCACTATGTTGTCCGGGCTGGGTCTTGAATTCCTGAGCTCAAGCAAT A G ZFPM2 Ensembl:ENSG00000169946 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs920212789 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86847,RMVar_hsa_circ_321766,RMVar_hsa_circ_307362,RMVar_hsa_circ_253833,RMVar_hsa_circ_253831,RMVar_hsa_circ_253832,RMVar_hsa_circ_336207,RMVar_hsa_circ_361480 51721 RMVar_ID_51721 Human_SNP_ID_376485438 A-to-I Human chr8 - 106001271 106001271 106001271 TGTAATCCCAGCCACCCGGGAGGCTGAGGCAGAAGAATCACTTGAACCTGGGAGGCGAAGTTTGC TGTAATCCCAGCCACCCGGGAGGCTGAGGCAGGAGAATCACTTGAACCTGGGAGGCGAAGTTTGC T C ZFPM2-AS1 Ensembl:ENSG00000251003 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1563627378 Functional Loss SNV dbSNP153 33..33 33 - - - 51722 RMVar_ID_51722 Human_SNP_ID_376558131 A-to-I Human chr8 + 106290073 106290073 106290073 CTCTTTCCTTCTTAAATTACCCAGTCTCAGGTATTTCTTCATAGCAGTGTGAGAATGGACTAATA CTCTTTCCTTCTTAAATTACCCAGTCTCAGGTGTTTCTTCATAGCAGTGTGAGAATGGACTAATA A G - - Other Unknown GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1480654279 Functional Loss SNV dbSNP153 33..33 33 - - - 51723 RMVar_ID_51723 Human_SNP_ID_376558594 A-to-I Human chr8 + 106291985 106291985 106291985 CCCTCCCACAACACGTGGGGATTATGGGAGCTACAATTCATGATGAGATTTGGATGGGGACACAG CCCTCCCACAACACGTGGGGATTATGGGAGCTGCAATTCATGATGAGATTTGGATGGGGACACAG A G - - Other Unknown GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs984457236 Functional Loss SNV dbSNP153 33..33 33 - - - 51724 RMVar_ID_51724 Human_SNP_ID_376588862 A-to-I Human chr8 + 106418460 106418460 106418460 CATCACTCAGAGATAACCACTGTCAACATTTTAGTGACTTTTCTTCTAACAAAATGTCTGATTTT CATCACTCAGAGATAACCACTGTCAACATTTTGGTGACTTTTCTTCTAACAAAATGTCTGATTTT A G OXR1 Ensembl:ENSG00000164830 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs925918668 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97391,RMVar_hsa_circ_253837 51725 RMVar_ID_51725 Human_SNP_ID_376600261 A-to-I Human chr8 + 106468337 106468337 106468337 TTTTGAGTTTACTTTAGTTACCATGTTCCCAGAAGACTTCTCTGAGGTGCCAACATTTGAGCGAG TTTTGAGTTTACTTTAGTTACCATGTTCCCAGTAGACTTCTCTGAGGTGCCAACATTTGAGCGAG A T OXR1 Ensembl:ENSG00000164830 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1402872257 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97391,RMVar_hsa_circ_253837 51726 RMVar_ID_51726 Human_SNP_ID_376659133 A-to-I Human chr8 + 106718937 106718937 106718937 ATGTTTTTAAACAATCAAGGCACAAAATGATTAAGGAAACCTTTCTTCATAGTGAACCAAACTTA ATGTTTTTAAACAATCAAGGCACAAAATGATTTAGGAAACCTTTCTTCATAGTGAACCAAACTTA A T OXR1 Ensembl:ENSG00000164830 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1390328375 Functional Loss SNV dbSNP153 33..33 33 - - - 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 51727 RMVar_ID_51727 Human_SNP_ID_376659521 A-to-I Human chr8 + 106720561 106720561 106720561 CTGCTGCATCAAAAACATAAATTTGGTTCACTATGGAAAAAGGTTTGTTTAATCATTTTGTGCCT CTGCTGCATCAAAAACATAAATTTGGTTCACTGTGGAAAAAGGTTTGTTTAATCATTTTGTGCCT A G OXR1 Ensembl:ENSG00000164830 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs907087448 Functional Loss SNV dbSNP153 33..33 33 - - - 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 51728 RMVar_ID_51728 Human_SNP_ID_376666311 A-to-I Human chr8 + 106749192 106749192 106749192 GTGAAATCCCATCTCTACTAAAAAACAGAAAAAATTAGCCGGGCGTGGTGGCAGGCACCTGTAGT GTGAAATCCCATCTCTACTAAAAAACAGAAAATATTAGCCGGGCGTGGTGGCAGGCACCTGTAGT A T OXR1 Ensembl:ENSG00000164830 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs558187021 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_97391,RMVar_hsa_circ_253837 51729 RMVar_ID_51729 Human_SNP_ID_377035171 A-to-I Human chr8 - 108218974 108218974 108218974 CGAGACCAGCCTGGCCAACACGGTGAAACCCCATCTCTACTAAAAATACAAAAAAGTTAGCCAGG CGAGACCAGCCTGGCCAACACGGTGAAACCCCGTCTCTACTAAAAATACAAAAAAGTTAGCCAGG T C EIF3E Ensembl:ENSG00000104408 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1317673097 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14759,RMVar_hsa_circ_92504,RMVar_hsa_circ_268554,RMVar_hsa_circ_253850,RMVar_hsa_circ_361844,RMVar_hsa_circ_90186,RMVar_hsa_circ_253853,RMVar_hsa_circ_253854,RMVar_hsa_circ_29048,RMVar_hsa_circ_253855,RMVar_hsa_circ_278820,RMVar_hsa_circ_329648,RMVar_hsa_circ_26538 51730 RMVar_ID_51730 Human_SNP_ID_377035176 A-to-I Human chr8 - 108218987 108218987 108218987 TGACTCAGCAGTTCGAGACCAGCCTGGCCAACACGGTGAAACCCCATCTCTACTAAAAATACAAA TGACTCAGCAGTTCGAGACCAGCCTGGCCAACTCGGTGAAACCCCATCTCTACTAAAAATACAAA T A EIF3E Ensembl:ENSG00000104408 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1215806209 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14759,RMVar_hsa_circ_92504,RMVar_hsa_circ_268554,RMVar_hsa_circ_253850,RMVar_hsa_circ_361844,RMVar_hsa_circ_90186,RMVar_hsa_circ_253853,RMVar_hsa_circ_253854,RMVar_hsa_circ_29048,RMVar_hsa_circ_253855,RMVar_hsa_circ_278820,RMVar_hsa_circ_329648,RMVar_hsa_circ_26538 51731 RMVar_ID_51731 Human_SNP_ID_377037077 A-to-I Human chr8 - 108226261 108226261 108226261 TGAGTTTGGGAGGTGGAGGTTGCAGTGAGCCTAGATCACACCATTGCACTCCAGCCTAGGCAACA TGAGTTTGGGAGGTGGAGGTTGCAGTGAGCCTGGATCACACCATTGCACTCCAGCCTAGGCAACA T C EIF3E Ensembl:ENSG00000104408 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1340413283 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14759,RMVar_hsa_circ_92504,RMVar_hsa_circ_268554,RMVar_hsa_circ_253850,RMVar_hsa_circ_361844,RMVar_hsa_circ_90186,RMVar_hsa_circ_253853,RMVar_hsa_circ_253854,RMVar_hsa_circ_29048,RMVar_hsa_circ_253855,RMVar_hsa_circ_278820,RMVar_hsa_circ_329648,RMVar_hsa_circ_26538 51732 RMVar_ID_51732 Human_SNP_ID_377354270 A-to-I Human chr8 + 109545637 109545637 109545637 TGCCCGCCTCAGCCTCCCAAAGCGCTGGGACTACAGACGTGAGCCACCGCGCCCAGCATAGTTTT TGCCCGCCTCAGCCTCCCAAAGCGCTGGGACTGCAGACGTGAGCCACCGCGCCCAGCATAGTTTT A G EBAG9 Ensembl:ENSG00000147654 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs886170804 Functional Loss SNV dbSNP153 33..33 33 - - - 51733 RMVar_ID_51733 Human_SNP_ID_377358183 A-to-I Human chr8 + 109562805 109562805 109562805 TATTTGTGTTCTGCTGCTAGTTCATCATCCCAAATATGAAAATCTAAAATCTGAAATGCTCCAAT TATTTGTGTTCTGCTGCTAGTTCATCATCCCAGATATGAAAATCTAAAATCTGAAATGCTCCAAT A G EBAG9 Ensembl:ENSG00000147654 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs570720430 Functional Loss SNV dbSNP153 33..33 33 - - - 51734 RMVar_ID_51734 Human_SNP_ID_378835559 A-to-I Human chr8 - 115535211 115535211 115535211 TATATATGCTATATATATATGCTATATATGCTATACATATGCTATATATATGCTATACATATGCT TATATATGCTATATATATATGCTATATATGCTGTACATATGCTATATATATGCTATACATATGCT T C TRPS1 Ensembl:ENSG00000104447 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1172012337 Functional Loss SNV dbSNP153 33..33 33 - - - 51735 RMVar_ID_51735 Human_SNP_ID_378835560 A-to-I Human chr8 - 115535211 115535211 115535211 TATATATGCTATATATATATGCTATATATGCTATACATATGCTATATATATGCTATACATATGCT TATATATGCTATATATATATGCTATATATGCTCTACATATGCTATATATATGCTATACATATGCT T G TRPS1 Ensembl:ENSG00000104447 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1172012337 Functional Loss SNV dbSNP153 33..33 33 - - - 51736 RMVar_ID_51736 Human_SNP_ID_378840935 A-to-I Human chr8 - 115557532 115557532 115557532 GGAAGCCCCTTATAAAACCATCAGCTCTCTCAAGAACTCAGTCACTATCACAAGGACAACAAGGG GGAAGCCCCTTATAAAACCATCAGCTCTCTCAGGAACTCAGTCACTATCACAAGGACAACAAGGG T C TRPS1 Ensembl:ENSG00000104447 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1231366200 Functional Loss SNV dbSNP153 33..33 33 - - - 51737 RMVar_ID_51737 Human_SNP_ID_378851641 A-to-I Human chr8 - 115604450 115604450 115604450 AGAATGATCTAGCCAAAAGTTCAGAAGGAGAGACAATGACCAAGACAGACAAGAGCTCGAGTGGG AGAATGATCTAGCCAAAAGTTCAGAAGGAGAGGCAATGACCAAGACAGACAAGAGCTCGAGTGGG T C TRPS1 Ensembl:ENSG00000104447 Protein coding CDS GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs376536580 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16323657 Human_miRNA_ID_2938467 RMVar_hsa_circ_308912,RMVar_hsa_circ_321704,RMVar_hsa_circ_279136,RMVar_hsa_circ_253975,RMVar_hsa_circ_253976,RMVar_hsa_circ_288916,RMVar_hsa_circ_295358,RMVar_hsa_circ_51034 51738 RMVar_ID_51738 Human_SNP_ID_378859611 A-to-I Human chr8 - 115639342 115639342 115639342 ATTGACTGTTGGACATCGTGGCTCACACCTGTAATCCCAGCACTCTGGAAGGCCAAGGTGGCAGG ATTGACTGTTGGACATCGTGGCTCACACCTGTGATCCCAGCACTCTGGAAGGCCAAGGTGGCAGG T C TRPS1 Ensembl:ENSG00000104447 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1309124689 Functional Loss SNV dbSNP153 33..33 33 - - - 51739 RMVar_ID_51739 Human_SNP_ID_379397492 A-to-I Human chr8 - 117908984 117908984 117908984 GGGATTACAGGCGCGTACAACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGATGAGGTTTCG GGGATTACAGGCGCGTACAACCACGCCCAGCTGATTTTTGTATTTTTAGTAGAGATGAGGTTTCG T C EXT1 Ensembl:ENSG00000182197 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1168165306 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114966,RMVar_hsa_circ_254006,RMVar_hsa_circ_101106,RMVar_hsa_circ_254012 51740 RMVar_ID_51740 Human_SNP_ID_379399300 A-to-I Human chr8 - 117916710 117916710 117916710 CGGGGTTTCACCATGTTGGCCAGACTAGTCTCAAACTCCTCACCTCAAGTGATCCTCCTGCCTTG CGGGGTTTCACCATGTTGGCCAGACTAGTCTCTAACTCCTCACCTCAAGTGATCCTCCTGCCTTG T A EXT1 Ensembl:ENSG00000182197 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs995545410 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114966,RMVar_hsa_circ_254006,RMVar_hsa_circ_101106,RMVar_hsa_circ_254012 51741 RMVar_ID_51741 Human_SNP_ID_379406298 A-to-I Human chr8 - 117945642 117945642 117945642 CAAAAATTAGCTGGGTATGGTGGTGGGCGCCTATAATCTCAGCTACTCCGGAGGCTGAGGATGGA CAAAAATTAGCTGGGTATGGTGGTGGGCGCCTGTAATCTCAGCTACTCCGGAGGCTGAGGATGGA T C EXT1 Ensembl:ENSG00000182197 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1035240261 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26147192 RMVar_hsa_circ_114966,RMVar_hsa_circ_254006,RMVar_hsa_circ_101106,RMVar_hsa_circ_254012 51742 RMVar_ID_51742 Human_SNP_ID_379408867 A-to-I Human chr8 - 117956581 117956578 117956581 AAAATTAGCCAGGTATGGTGATGCGTGCCTGTAGTCCCAGCTATTTGGGAGGCTGAGGCAGGAGA AAAATTAGCCAGGTATGGTGATGCGTGCCTGT___CCCAGCTATTTGGGAGGCTGAGGCAGGAGA GACT G EXT1 Ensembl:ENSG00000182197 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1245574701 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_114966,RMVar_hsa_circ_254006,RMVar_hsa_circ_101106,RMVar_hsa_circ_254012 51743 RMVar_ID_51743 Human_SNP_ID_379413031 A-to-I Human chr8 - 117973586 117973586 117973586 TGTTTAAATTATTTTGGAGTCAGGGACTCATTATGTTGCCCAGACTGATCTTGAACTCCTAGGCT TGTTTAAATTATTTTGGAGTCAGGGACTCATTGTGTTGCCCAGACTGATCTTGAACTCCTAGGCT T C EXT1 Ensembl:ENSG00000182197 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1048333915 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17578707 RMVar_hsa_circ_114966,RMVar_hsa_circ_254006,RMVar_hsa_circ_101106,RMVar_hsa_circ_254012 51744 RMVar_ID_51744 Human_SNP_ID_379415575 A-to-I Human chr8 - 117983397 117983397 117983397 TCACTGTAGCGCCAACCTCCTGGGCTCAAGCAATCTTCTCACCTCAGCCTCTTGAGTAGGTGGGA TCACTGTAGCGCCAACCTCCTGGGCTCAAGCAGTCTTCTCACCTCAGCCTCTTGAGTAGGTGGGA T C EXT1 Ensembl:ENSG00000182197 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1486212485 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8678543 RMVar_hsa_circ_114966,RMVar_hsa_circ_254006,RMVar_hsa_circ_101106,RMVar_hsa_circ_254012 51745 RMVar_ID_51745 Human_SNP_ID_379416391 A-to-I Human chr8 - 117986368 117986368 117986368 TTGGTCAACATGTCAAAACCCCTCTCTGCTAAAAGTACAAAAACTTAGCCAGGCGTGGTGGTGCA TTGGTCAACATGTCAAAACCCCTCTCTGCTAACAGTACAAAAACTTAGCCAGGCGTGGTGGTGCA T G EXT1 Ensembl:ENSG00000182197 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1347391237 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17578710 RMVar_hsa_circ_114966,RMVar_hsa_circ_254006,RMVar_hsa_circ_101106,RMVar_hsa_circ_254012 51746 RMVar_ID_51746 Human_SNP_ID_379416727 A-to-I Human chr8 - 117987837 117987837 117987837 GCGATCCTTCCGCCTAGGCCTCTCAAAGTTCTAGGATTATAGGCATGAGCCACAGCACCTGACCA GCGATCCTTCCGCCTAGGCCTCTCAAAGTTCTGGGATTATAGGCATGAGCCACAGCACCTGACCA T C EXT1 Ensembl:ENSG00000182197 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1277316905 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114966,RMVar_hsa_circ_254006,RMVar_hsa_circ_101106,RMVar_hsa_circ_254012 51747 RMVar_ID_51747 Human_SNP_ID_379416745 A-to-I Human chr8 - 117987905 117987905 117987905 TTTGGTATTTTTTGTAGAGACGAGATTTTGCTATGTTGCCCAGGCTGGTCTCAAACTCCTGGGTC TTTGGTATTTTTTGTAGAGACGAGATTTTGCTGTGTTGCCCAGGCTGGTCTCAAACTCCTGGGTC T C EXT1 Ensembl:ENSG00000182197 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs568388316 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16330556 RMVar_hsa_circ_114966,RMVar_hsa_circ_254006,RMVar_hsa_circ_101106,RMVar_hsa_circ_254012 51748 RMVar_ID_51748 Human_SNP_ID_379416771 A-to-I Human chr8 - 117988074 117988070 117988074 TGTATGTATTTATTTATTTGTGACAGGATCTCACTCTGTTGCTCAGGCTGGAGTGCAATGGCACC TGTATGTATTTATTTATTTGTGACAGGATCTC____TGTTGCTCAGGCTGGAGTGCAATGGCACC AGAGT A EXT1 Ensembl:ENSG00000182197 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs145608302 Functional Loss DEL dbSNP153 33..36 33 - - - RMVar_hsa_circ_114966,RMVar_hsa_circ_254006,RMVar_hsa_circ_101106,RMVar_hsa_circ_254012 51749 RMVar_ID_51749 Human_SNP_ID_379419324 A-to-I Human chr8 - 117998576 117998576 117998576 CTTAAAAAATGCAGAATTTTAGGCTGGGCACAATAGTTCATGCCTGTAATCCCAGCACTTTGGGA CTTAAAAAATGCAGAATTTTAGGCTGGGCACAGTAGTTCATGCCTGTAATCCCAGCACTTTGGGA T C EXT1 Ensembl:ENSG00000182197 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1370127423 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_14906 RMVar_hsa_circ_114966,RMVar_hsa_circ_254006,RMVar_hsa_circ_101106,RMVar_hsa_circ_254012 51750 RMVar_ID_51750 Human_SNP_ID_379426685 A-to-I Human chr8 - 118029246 118029246 118029246 ATTTTTATTTTTTGTAGAGACTGGGTCTTACTATGTTGCACATGCTGGTCTTGAACTCCTGGCTT ATTTTTATTTTTTGTAGAGACTGGGTCTTACTGTGTTGCACATGCTGGTCTTGAACTCCTGGCTT T C EXT1 Ensembl:ENSG00000182197 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1401606377 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23199010 RMVar_hsa_circ_114966,RMVar_hsa_circ_254006,RMVar_hsa_circ_101106,RMVar_hsa_circ_254012 51751 RMVar_ID_51751 Human_SNP_ID_379427002 A-to-I Human chr8 - 118030664 118030664 118030664 CAGCCTGACCAACATGGTGAAACCCCATCTCTACTAAGTACAAAAAAATTAGCTGGGCGTGGTGG CAGCCTGACCAACATGGTGAAACCCCATCTCTCCTAAGTACAAAAAAATTAGCTGGGCGTGGTGG T G EXT1 Ensembl:ENSG00000182197 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1309979624 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23199011 RMVar_hsa_circ_114966,RMVar_hsa_circ_254006,RMVar_hsa_circ_101106,RMVar_hsa_circ_254012 51752 RMVar_ID_51752 Human_SNP_ID_379427220 A-to-I Human chr8 - 118031462 118031462 118031462 AGAGTACAATGACTCGATCTCAGCTCACTGCAACCTCCGCCTTGCAGGTTCAAGCAATTCCCCTG AGAGTACAATGACTCGATCTCAGCTCACTGCAGCCTCCGCCTTGCAGGTTCAAGCAATTCCCCTG T C EXT1 Ensembl:ENSG00000182197 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1252115597 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16331729 RMVar_hsa_circ_114966,RMVar_hsa_circ_254006,RMVar_hsa_circ_101106,RMVar_hsa_circ_254012 51753 RMVar_ID_51753 Human_SNP_ID_379444303 A-to-I Human chr8 - 118103071 118103071 118103071 TCGGCTTACCGCAACCTCCTCCTCCCGGATTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGC TCGGCTTACCGCAACCTCCTCCTCCCGGATTCGAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGC T C EXT1 Ensembl:ENSG00000182197 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1304179838 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_114966,RMVar_hsa_circ_254006,RMVar_hsa_circ_101106,RMVar_hsa_circ_254012 51754 RMVar_ID_51754 Human_SNP_ID_379492180 A-to-I Human chr8 - 118300800 118300800 118300800 ATATACAATTTTATGAACATGCGCTACCTATCAGTAATCTGTAATATTTAAGAATTAACAAAAAA ATATACAATTTTATGAACATGCGCTACCTATCCGTAATCTGTAATATTTAAGAATTAACAAAAAA T G SAMD12 Ensembl:ENSG00000177570 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1351074908 Functional Loss SNV dbSNP153 33..33 33 - - - 51755 RMVar_ID_51755 Human_SNP_ID_379492182 A-to-I Human chr8 - 118300807 118300807 118300807 CAGAAGAATATACAATTTTATGAACATGCGCTACCTATCAGTAATCTGTAATATTTAAGAATTAA CAGAAGAATATACAATTTTATGAACATGCGCTGCCTATCAGTAATCTGTAATATTTAAGAATTAA T C SAMD12 Ensembl:ENSG00000177570 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs933139300 Functional Loss SNV dbSNP153 33..33 33 - - - 51756 RMVar_ID_51756 Human_SNP_ID_379502084 A-to-I Human chr8 - 118341553 118341553 118341553 GCTGGCATCCTGATCCCAGACATTCAGCCTCTAGAACCATGAGAGATAAATTTCTGTGGTTTATA GCTGGCATCCTGATCCCAGACATTCAGCCTCTCGAACCATGAGAGATAAATTTCTGTGGTTTATA T G SAMD12 Ensembl:ENSG00000177570 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs914332254 Functional Loss SNV dbSNP153 33..33 33 - - - 51757 RMVar_ID_51757 Human_SNP_ID_379504079 A-to-I Human chr8 - 118349893 118349893 118349893 AAACTCCTGGGCTCAAGCAATCCTCCCAGCTTAGCTTCCCAAGGTACTGGGATTACAGGTGTGAG AAACTCCTGGGCTCAAGCAATCCTCCCAGCTTGGCTTCCCAAGGTACTGGGATTACAGGTGTGAG T C SAMD12 Ensembl:ENSG00000177570 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1267578890 Functional Loss SNV dbSNP153 33..33 33 - - - 51758 RMVar_ID_51758 Human_SNP_ID_379866729 A-to-I Human chr8 - 119794020 119794020 119794020 CTTGGGCTGAGGTGGGAGGATCACCTAAGCCCAGGAAGTCAAGGCTGCAGTAAGCCATAATCAGC CTTGGGCTGAGGTGGGAGGATCACCTAAGCCCGGGAAGTCAAGGCTGCAGTAAGCCATAATCAGC T C TAF2 Ensembl:ENSG00000064313 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1429884721 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17578716 RMVar_hsa_circ_184,RMVar_hsa_circ_51999,RMVar_hsa_circ_366478,RMVar_hsa_circ_346334,RMVar_hsa_circ_111084,RMVar_hsa_circ_52752,RMVar_hsa_circ_125993,RMVar_hsa_circ_254040,RMVar_hsa_circ_123611,RMVar_hsa_circ_254043,RMVar_hsa_circ_87168,RMVar_hsa_circ_254044,RMVar_hsa_circ_254045,RMVar_hsa_circ_38645,RMVar_hsa_circ_349210,RMVar_hsa_circ_362514,RMVar_hsa_circ_323830,RMVar_hsa_circ_72591,RMVar_hsa_circ_254050,RMVar_hsa_circ_254051,RMVar_hsa_circ_375900,RMVar_hsa_circ_106804,RMVar_hsa_circ_61151,RMVar_hsa_circ_92193,RMVar_hsa_circ_52579,RMVar_hsa_circ_18025,RMVar_hsa_circ_108,RMVar_hsa_circ_254055,RMVar_hsa_circ_254056,RMVar_hsa_circ_254054,RMVar_hsa_circ_56037,RMVar_hsa_circ_22763,RMVar_hsa_circ_367127,RMVar_hsa_circ_287163,RMVar_hsa_circ_352352,RMVar_hsa_circ_254057,RMVar_hsa_circ_354248,RMVar_hsa_circ_317661,RMVar_hsa_circ_308936,RMVar_hsa_circ_254064,RMVar_hsa_circ_254066,RMVar_hsa_circ_254065,RMVar_hsa_circ_254063,RMVar_hsa_circ_40005,RMVar_hsa_circ_48080,RMVar_hsa_circ_29764,RMVar_hsa_circ_31870,RMVar_hsa_circ_36447,RMVar_hsa_circ_46888,RMVar_hsa_circ_254067,RMVar_hsa_circ_33376,RMVar_hsa_circ_271445,RMVar_hsa_circ_62191,RMVar_hsa_circ_71780,RMVar_hsa_circ_254073,RMVar_hsa_circ_271478,RMVar_hsa_circ_254075,RMVar_hsa_circ_316294,RMVar_hsa_circ_316086,RMVar_hsa_circ_324389,RMVar_hsa_circ_254074,RMVar_hsa_circ_358560,RMVar_hsa_circ_295231,RMVar_hsa_circ_254076,RMVar_hsa_circ_254077 51759 RMVar_ID_51759 Human_SNP_ID_379866747 A-to-I Human chr8 - 119794073 119794073 119794073 TTTTTTTCTTTTAATTAACCAGGCACGGTGGCATGTGCCTGTAGTTCCAGCTTCTTGGGCTGAGG TTTTTTTCTTTTAATTAACCAGGCACGGTGGCGTGTGCCTGTAGTTCCAGCTTCTTGGGCTGAGG T C TAF2 Ensembl:ENSG00000064313 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1359432715 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17578716 RMVar_hsa_circ_184,RMVar_hsa_circ_51999,RMVar_hsa_circ_366478,RMVar_hsa_circ_346334,RMVar_hsa_circ_111084,RMVar_hsa_circ_52752,RMVar_hsa_circ_125993,RMVar_hsa_circ_254040,RMVar_hsa_circ_123611,RMVar_hsa_circ_254043,RMVar_hsa_circ_87168,RMVar_hsa_circ_254044,RMVar_hsa_circ_254045,RMVar_hsa_circ_38645,RMVar_hsa_circ_349210,RMVar_hsa_circ_362514,RMVar_hsa_circ_323830,RMVar_hsa_circ_72591,RMVar_hsa_circ_254050,RMVar_hsa_circ_254051,RMVar_hsa_circ_375900,RMVar_hsa_circ_106804,RMVar_hsa_circ_61151,RMVar_hsa_circ_92193,RMVar_hsa_circ_52579,RMVar_hsa_circ_18025,RMVar_hsa_circ_108,RMVar_hsa_circ_254055,RMVar_hsa_circ_254056,RMVar_hsa_circ_254054,RMVar_hsa_circ_56037,RMVar_hsa_circ_22763,RMVar_hsa_circ_367127,RMVar_hsa_circ_287163,RMVar_hsa_circ_352352,RMVar_hsa_circ_254057,RMVar_hsa_circ_354248,RMVar_hsa_circ_317661,RMVar_hsa_circ_308936,RMVar_hsa_circ_254064,RMVar_hsa_circ_254066,RMVar_hsa_circ_254065,RMVar_hsa_circ_254063,RMVar_hsa_circ_40005,RMVar_hsa_circ_48080,RMVar_hsa_circ_29764,RMVar_hsa_circ_31870,RMVar_hsa_circ_36447,RMVar_hsa_circ_46888,RMVar_hsa_circ_254067,RMVar_hsa_circ_33376,RMVar_hsa_circ_271445,RMVar_hsa_circ_62191,RMVar_hsa_circ_71780,RMVar_hsa_circ_254073,RMVar_hsa_circ_271478,RMVar_hsa_circ_254075,RMVar_hsa_circ_316294,RMVar_hsa_circ_316086,RMVar_hsa_circ_324389,RMVar_hsa_circ_254074,RMVar_hsa_circ_358560,RMVar_hsa_circ_295231,RMVar_hsa_circ_254076,RMVar_hsa_circ_254077 51760 RMVar_ID_51760 Human_SNP_ID_379866811 A-to-I Human chr8 - 119794333 119794333 119794333 GTAGTGCAGTGGCGCAATCTCGGCTCACTGCAACCTCTGCCTCCCGGGCTTAAGCGATTCTTCCA GTAGTGCAGTGGCGCAATCTCGGCTCACTGCAGCCTCTGCCTCCCGGGCTTAAGCGATTCTTCCA T C TAF2 Ensembl:ENSG00000064313 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924467073 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_184,RMVar_hsa_circ_51999,RMVar_hsa_circ_366478,RMVar_hsa_circ_346334,RMVar_hsa_circ_111084,RMVar_hsa_circ_52752,RMVar_hsa_circ_125993,RMVar_hsa_circ_254040,RMVar_hsa_circ_123611,RMVar_hsa_circ_254043,RMVar_hsa_circ_87168,RMVar_hsa_circ_254044,RMVar_hsa_circ_254045,RMVar_hsa_circ_38645,RMVar_hsa_circ_349210,RMVar_hsa_circ_362514,RMVar_hsa_circ_323830,RMVar_hsa_circ_72591,RMVar_hsa_circ_254050,RMVar_hsa_circ_254051,RMVar_hsa_circ_375900,RMVar_hsa_circ_106804,RMVar_hsa_circ_61151,RMVar_hsa_circ_92193,RMVar_hsa_circ_52579,RMVar_hsa_circ_18025,RMVar_hsa_circ_108,RMVar_hsa_circ_254055,RMVar_hsa_circ_254056,RMVar_hsa_circ_254054,RMVar_hsa_circ_56037,RMVar_hsa_circ_22763,RMVar_hsa_circ_367127,RMVar_hsa_circ_287163,RMVar_hsa_circ_352352,RMVar_hsa_circ_254057,RMVar_hsa_circ_354248,RMVar_hsa_circ_317661,RMVar_hsa_circ_308936,RMVar_hsa_circ_254064,RMVar_hsa_circ_254066,RMVar_hsa_circ_254065,RMVar_hsa_circ_254063,RMVar_hsa_circ_40005,RMVar_hsa_circ_48080,RMVar_hsa_circ_29764,RMVar_hsa_circ_31870,RMVar_hsa_circ_36447,RMVar_hsa_circ_46888,RMVar_hsa_circ_254067,RMVar_hsa_circ_33376,RMVar_hsa_circ_271445,RMVar_hsa_circ_62191,RMVar_hsa_circ_71780,RMVar_hsa_circ_254073,RMVar_hsa_circ_271478,RMVar_hsa_circ_254075,RMVar_hsa_circ_316294,RMVar_hsa_circ_316086,RMVar_hsa_circ_324389,RMVar_hsa_circ_254074,RMVar_hsa_circ_358560,RMVar_hsa_circ_295231,RMVar_hsa_circ_254076,RMVar_hsa_circ_254077 51761 RMVar_ID_51761 Human_SNP_ID_379866812 A-to-I Human chr8 - 119794333 119794333 119794333 GTAGTGCAGTGGCGCAATCTCGGCTCACTGCAACCTCTGCCTCCCGGGCTTAAGCGATTCTTCCA GTAGTGCAGTGGCGCAATCTCGGCTCACTGCACCCTCTGCCTCCCGGGCTTAAGCGATTCTTCCA T G TAF2 Ensembl:ENSG00000064313 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs924467073 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_184,RMVar_hsa_circ_51999,RMVar_hsa_circ_366478,RMVar_hsa_circ_346334,RMVar_hsa_circ_111084,RMVar_hsa_circ_52752,RMVar_hsa_circ_125993,RMVar_hsa_circ_254040,RMVar_hsa_circ_123611,RMVar_hsa_circ_254043,RMVar_hsa_circ_87168,RMVar_hsa_circ_254044,RMVar_hsa_circ_254045,RMVar_hsa_circ_38645,RMVar_hsa_circ_349210,RMVar_hsa_circ_362514,RMVar_hsa_circ_323830,RMVar_hsa_circ_72591,RMVar_hsa_circ_254050,RMVar_hsa_circ_254051,RMVar_hsa_circ_375900,RMVar_hsa_circ_106804,RMVar_hsa_circ_61151,RMVar_hsa_circ_92193,RMVar_hsa_circ_52579,RMVar_hsa_circ_18025,RMVar_hsa_circ_108,RMVar_hsa_circ_254055,RMVar_hsa_circ_254056,RMVar_hsa_circ_254054,RMVar_hsa_circ_56037,RMVar_hsa_circ_22763,RMVar_hsa_circ_367127,RMVar_hsa_circ_287163,RMVar_hsa_circ_352352,RMVar_hsa_circ_254057,RMVar_hsa_circ_354248,RMVar_hsa_circ_317661,RMVar_hsa_circ_308936,RMVar_hsa_circ_254064,RMVar_hsa_circ_254066,RMVar_hsa_circ_254065,RMVar_hsa_circ_254063,RMVar_hsa_circ_40005,RMVar_hsa_circ_48080,RMVar_hsa_circ_29764,RMVar_hsa_circ_31870,RMVar_hsa_circ_36447,RMVar_hsa_circ_46888,RMVar_hsa_circ_254067,RMVar_hsa_circ_33376,RMVar_hsa_circ_271445,RMVar_hsa_circ_62191,RMVar_hsa_circ_71780,RMVar_hsa_circ_254073,RMVar_hsa_circ_271478,RMVar_hsa_circ_254075,RMVar_hsa_circ_316294,RMVar_hsa_circ_316086,RMVar_hsa_circ_324389,RMVar_hsa_circ_254074,RMVar_hsa_circ_358560,RMVar_hsa_circ_295231,RMVar_hsa_circ_254076,RMVar_hsa_circ_254077 51762 RMVar_ID_51762 Human_SNP_ID_379869199 A-to-I Human chr8 - 119803635 119803635 119803635 TGTTGGAATACACTGGGGTGCTATCTCTGCTCACTGCAACCTGTGCCTCCTGGGTTCAAGTGATT TGTTGGAATACACTGGGGTGCTATCTCTGCTCGCTGCAACCTGTGCCTCCTGGGTTCAAGTGATT T C TAF2 Ensembl:ENSG00000064313 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1264156068 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16335639 RMVar_hsa_circ_184,RMVar_hsa_circ_51999,RMVar_hsa_circ_346334,RMVar_hsa_circ_111084,RMVar_hsa_circ_125993,RMVar_hsa_circ_254040,RMVar_hsa_circ_254045,RMVar_hsa_circ_349210,RMVar_hsa_circ_362514,RMVar_hsa_circ_72591,RMVar_hsa_circ_61151,RMVar_hsa_circ_92193,RMVar_hsa_circ_52579,RMVar_hsa_circ_254056,RMVar_hsa_circ_22763,RMVar_hsa_circ_352352,RMVar_hsa_circ_354248,RMVar_hsa_circ_317661,RMVar_hsa_circ_254066,RMVar_hsa_circ_254065,RMVar_hsa_circ_40005,RMVar_hsa_circ_48080,RMVar_hsa_circ_31870,RMVar_hsa_circ_36447,RMVar_hsa_circ_46888,RMVar_hsa_circ_62191,RMVar_hsa_circ_254075,RMVar_hsa_circ_324389,RMVar_hsa_circ_7303,RMVar_hsa_circ_254077,RMVar_hsa_circ_16837,RMVar_hsa_circ_356898,RMVar_hsa_circ_374308,RMVar_hsa_circ_254080,RMVar_hsa_circ_254081 51763 RMVar_ID_51763 Human_SNP_ID_379871889 A-to-I Human chr8 - 119813933 119813933 119813933 TTTTTATTTTTTACTGGATGCATGGTCTCACTATGTTGCCTAAACTGGTTTTGAACTCCTGGCCT TTTTTATTTTTTACTGGATGCATGGTCTCACTGTGTTGCCTAAACTGGTTTTGAACTCCTGGCCT T C TAF2 Ensembl:ENSG00000064313 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1254744931 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16335852 RMVar_hsa_circ_184,RMVar_hsa_circ_346334,RMVar_hsa_circ_349210,RMVar_hsa_circ_61151,RMVar_hsa_circ_92193,RMVar_hsa_circ_254056,RMVar_hsa_circ_22763,RMVar_hsa_circ_317661,RMVar_hsa_circ_254066,RMVar_hsa_circ_36447,RMVar_hsa_circ_254075,RMVar_hsa_circ_254077,RMVar_hsa_circ_374308,RMVar_hsa_circ_66944,RMVar_hsa_circ_254080,RMVar_hsa_circ_254081,RMVar_hsa_circ_254083,RMVar_hsa_circ_315317,RMVar_hsa_circ_254084,RMVar_hsa_circ_254085 51764 RMVar_ID_51764 Human_SNP_ID_379871920 A-to-I Human chr8 - 119814029 119814029 119814029 AGCCTTGAACTTCTGCACTGAAGCCATCATCTACCTTAGCTTCTCGAGTAGCTGGAACAATATGT AGCCTTGAACTTCTGCACTGAAGCCATCATCTGCCTTAGCTTCTCGAGTAGCTGGAACAATATGT T C TAF2 Ensembl:ENSG00000064313 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1187145913 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_184,RMVar_hsa_circ_346334,RMVar_hsa_circ_349210,RMVar_hsa_circ_61151,RMVar_hsa_circ_92193,RMVar_hsa_circ_254056,RMVar_hsa_circ_22763,RMVar_hsa_circ_317661,RMVar_hsa_circ_254066,RMVar_hsa_circ_36447,RMVar_hsa_circ_254075,RMVar_hsa_circ_254077,RMVar_hsa_circ_374308,RMVar_hsa_circ_66944,RMVar_hsa_circ_254080,RMVar_hsa_circ_254081,RMVar_hsa_circ_254083,RMVar_hsa_circ_315317,RMVar_hsa_circ_254084,RMVar_hsa_circ_254085 51765 RMVar_ID_51765 Human_SNP_ID_379875151 A-to-I Human chr8 - 119826618 119826618 119826618 CTGCTGCACTCCAGCCTGGACAACAAGAGTGAAACCCCATCTCAAAAAAAAAAAAGGAGGAAATG CTGCTGCACTCCAGCCTGGACAACAAGAGTGATACCCCATCTCAAAAAAAAAAAAGGAGGAAATG T A TAF2 Ensembl:ENSG00000064313 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1166454421 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92193,RMVar_hsa_circ_254056,RMVar_hsa_circ_254075,RMVar_hsa_circ_254077,RMVar_hsa_circ_254081,RMVar_hsa_circ_254085 51766 RMVar_ID_51766 Human_SNP_ID_379880047 A-to-I Human chr8 - 119846242 119846242 119846242 AGGCGTGGTGGTGGGTGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCCCTTGAA AGGCGTGGTGGTGGGTGCCTGTAATCCCAGCTGCTCAGGAGGCTGAGGCAGGAGAATCCCTTGAA T C DSCC1 Ensembl:ENSG00000136982 Protein coding intron GSE38233;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;Bronchiolar epithelium,BERP35T4 cell line - 24183664,31158229 RNA-Seq:(High) rs1387548373 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_292596,RMVar_hsa_circ_309861,RMVar_hsa_circ_81560,RMVar_hsa_circ_254091,RMVar_hsa_circ_254092 51767 RMVar_ID_51767 Human_SNP_ID_357712915 A-to-I Human chr8 + 30069858 30069852 30069858 GTTACAGGAATCCGCCGAGGACCACTTATAATAATAATCAGAGAAAGAGGCAAAGCCGTGCTGCT GTTACAGGAATCCGCCGAGGACCACTT______ATAATCAGAGAAAGAGGCAAAGCCGTGCTGCT TATAATA T lnc-LEPROTL1-7 RNACentral:URS00008BFCCF lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs776307664 Functional Loss DEL dbSNP153 28..33 33 - - - 51768 RMVar_ID_51768 Human_SNP_ID_357716100 A-to-I Human chr8 - 30082299 30082299 30082299 GAGTCTCACATTGTCGCCCCGGCCGCACTGCAATGACGTGATCTCGGCTCACTGCAACCTCCGCC GAGTCTCACATTGTCGCCCCGGCCGCACTGCAGTGACGTGATCTCGGCTCACTGCAACCTCCGCC T C SARAF Ensembl:ENSG00000133872 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1039217525 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_963165 RMVar_hsa_circ_128053,RMVar_hsa_circ_251071 51769 RMVar_ID_51769 Human_SNP_ID_357723079 A-to-I Human chr8 + 30107620 30107620 30107620 GGAAGCAGGACGAAATATCGGCGTGTGGCTGGAGCCTTCCCACTGGAGGCTGAAAGTGGCTTGTG GGAAGCAGGACGAAATATCGGCGTGTGGCTGGGGCCTTCCCACTGGAGGCTGAAAGTGGCTTGTG A G LEPROTL1 Ensembl:ENSG00000104660 Protein coding 3'UTR GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1372540933 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_698367,Human_RBP_ID_7830559,Human_RBP_ID_18124850,Human_RBP_ID_24255252 Human_miRNA_ID_2973448,Human_miRNA_ID_3006636 RMVar_hsa_circ_82577,RMVar_hsa_circ_94537,RMVar_hsa_circ_376437,RMVar_hsa_circ_251073,RMVar_hsa_circ_251077,RMVar_hsa_circ_251078,RMVar_hsa_circ_120391,RMVar_hsa_circ_251081,RMVar_hsa_circ_103842,RMVar_hsa_circ_251083 51770 RMVar_ID_51770 Human_SNP_ID_357724459 A-to-I Human chr8 + 30113155 30113155 30113155 AAAATTAGCCGGGTGTGGTGGCTCATGACTGTAATCCCAGCTACTCCGGAAGCTGCGGCAGGAGA AAAATTAGCCGGGTGTGGTGGCTCATGACTGTTATCCCAGCTACTCCGGAAGCTGCGGCAGGAGA A T LEPROTL1 Ensembl:ENSG00000104660 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1295846846 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_82577,RMVar_hsa_circ_94537,RMVar_hsa_circ_251073,RMVar_hsa_circ_251078 51771 RMVar_ID_51771 Human_SNP_ID_357725519 A-to-I Human chr8 - 30117557 30117557 30117557 GTGAACCTCACAGACAGGCTAAACAAGTGTGGAGTGATCAGCCCCAGATTTGATGTGCAACTCAA GTGAACCTCACAGACAGGCTAAACAAGTGTGGGGTGATCAGCCCCAGATTTGATGTGCAACTCAA T C RPS15AP24 Ensembl:ENSG00000241511 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs878944182 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_182150,Human_RBP_ID_26559073 51772 RMVar_ID_51772 Human_SNP_ID_357738765 A-to-I Human chr8 + 30171379 30171379 30171379 TCAAGCAATCCTCCCACCTCAGCCTCCCAAGTAGTTGGGACCACAGGTGCACCCCACCATAACTG TCAAGCAATCCTCCCACCTCAGCCTCCCAAGTGGTTGGGACCACAGGTGCACCCCACCATAACTG A G LEPROTL1,DCTN6 Ensembl:ENSG00000104660,Ensembl:ENSG00000104671 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs764397665 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18895745 RMVar_hsa_circ_251084,RMVar_hsa_circ_303438,RMVar_hsa_circ_251085 51773 RMVar_ID_51773 Human_SNP_ID_357740443 A-to-I Human chr8 + 30178745 30178745 30178745 GCAGTGGCACAATCATAGCTTACTGCAGCCTCAGCTCCCAGACTCAAGCAATCCTTCCATCTCAG GCAGTGGCACAATCATAGCTTACTGCAGCCTCGGCTCCCAGACTCAAGCAATCCTTCCATCTCAG A G DCTN6 Ensembl:ENSG00000104671 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1324879610 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79918,RMVar_hsa_circ_251084,RMVar_hsa_circ_303438,RMVar_hsa_circ_282120,RMVar_hsa_circ_251086,RMVar_hsa_circ_251087,RMVar_hsa_circ_276605,RMVar_hsa_circ_99394,RMVar_hsa_circ_251089,RMVar_hsa_circ_251091,RMVar_hsa_circ_251092,RMVar_hsa_circ_251090 51774 RMVar_ID_51774 Human_SNP_ID_357740455 A-to-I Human chr8 + 30178794 30178794 30178794 AATCCTTCCATCTCAGCCTCCCAAGTAGCTGGAATTATAGGTGCACACCACCGTGCCCAGCTAAT AATCCTTCCATCTCAGCCTCCCAAGTAGCTGGCATTATAGGTGCACACCACCGTGCCCAGCTAAT A C DCTN6 Ensembl:ENSG00000104671 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs996364128 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79918,RMVar_hsa_circ_251084,RMVar_hsa_circ_303438,RMVar_hsa_circ_282120,RMVar_hsa_circ_251086,RMVar_hsa_circ_251087,RMVar_hsa_circ_276605,RMVar_hsa_circ_99394,RMVar_hsa_circ_251089,RMVar_hsa_circ_251091,RMVar_hsa_circ_251092,RMVar_hsa_circ_251090 51775 RMVar_ID_51775 Human_SNP_ID_357740462 A-to-I Human chr8 + 30178824 30178824 30178824 GGAATTATAGGTGCACACCACCGTGCCCAGCTAATTTTATTTTTGGTAGAGATGGTGTCTCACTC GGAATTATAGGTGCACACCACCGTGCCCAGCTGATTTTATTTTTGGTAGAGATGGTGTCTCACTC A G DCTN6 Ensembl:ENSG00000104671 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1197921613 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79918,RMVar_hsa_circ_251084,RMVar_hsa_circ_303438,RMVar_hsa_circ_282120,RMVar_hsa_circ_251086,RMVar_hsa_circ_251087,RMVar_hsa_circ_276605,RMVar_hsa_circ_99394,RMVar_hsa_circ_251089,RMVar_hsa_circ_251091,RMVar_hsa_circ_251092,RMVar_hsa_circ_251090 51776 RMVar_ID_51776 Human_SNP_ID_357741338 A-to-I Human chr8 + 30182854 30182854 30182854 CTTCCACCTCAGCCTCCTGAGTAGCTATGACTACAGGGGTGTGCCACCACACACAGCTAATTTTT CTTCCACCTCAGCCTCCTGAGTAGCTATGACTTCAGGGGTGTGCCACCACACACAGCTAATTTTT A T DCTN6 Ensembl:ENSG00000104671 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335072796 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_251084,RMVar_hsa_circ_251087,RMVar_hsa_circ_99394,RMVar_hsa_circ_251091,RMVar_hsa_circ_251092 51777 RMVar_ID_51777 Human_SNP_ID_357741586 A-to-I Human chr8 + 30184118 30184118 30184118 TTTATTTATTTTAGAGACAAGGATCTCACTCTATTACCTAGGCTGGAGTGCAGTGGCACAGTCTG TTTATTTATTTTAGAGACAAGGATCTCACTCTGTTACCTAGGCTGGAGTGCAGTGGCACAGTCTG A G RF00017-4490 RNACentral:URS0000922AF7 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs772630700 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16402689 RMVar_hsa_circ_251084,RMVar_hsa_circ_251087,RMVar_hsa_circ_251092 51778 RMVar_ID_51778 Human_SNP_ID_357741930 A-to-I Human chr8 - 30185853 30185851 30185854 GCCATGTCAAGAGAACACCCAGGTAGCCTTGTAGAGAGGCTCATGTGATGATGAACTGAGGCCTT GCCATGTCAAGAGAACACCCAGGTAGCCTTG___AGAGGCTCATGTGATGATGAACTGAGGCCTT TCTA T - - Other Unknown GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1382630074 Functional Loss DEL dbSNP153 32..34 33 - - - 51779 RMVar_ID_51779 Human_SNP_ID_357742054 A-to-I Human chr8 + 30186358 30186358 30186358 GCTGGTCTCGAACTCCTGACCTCGGGTGATCCACCTGCCTCAGCCTCCCAAAGTGCTGGGATTAC GCTGGTCTCGAACTCCTGACCTCGGGTGATCCGCCTGCCTCAGCCTCCCAAAGTGCTGGGATTAC A G RF00017-4490 RNACentral:URS0000922AF7 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1351305282 Functional Loss SNV dbSNP153 33..33 33 - - - 51780 RMVar_ID_51780 Human_SNP_ID_357742549 A-to-I Human chr8 + 30188736 30188735 30188737 AGAGTTTTATTTATTTATTTTTATTTGAAGACAGGGGCTGGCTCTGTTACCCAGGCTGGAAAACA AGAGTTTTATTTATTTATTTTTATTTGAAGAC__GGGCTGGCTCTGTTACCCAGGCTGGAAAACA CAG C RF00017-4490 RNACentral:URS0000922AF7 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1200618369 Functional Loss DEL dbSNP153 33..34 33 - - - Human_RBP_ID_7830766,Human_RBP_ID_16402780 51781 RMVar_ID_51781 Human_SNP_ID_357742550 A-to-I Human chr8 + 30188736 30188736 30188736 AGAGTTTTATTTATTTATTTTTATTTGAAGACAGGGGCTGGCTCTGTTACCCAGGCTGGAAAACA AGAGTTTTATTTATTTATTTTTATTTGAAGACGGGGGCTGGCTCTGTTACCCAGGCTGGAAAACA A G RF00017-4490 RNACentral:URS0000922AF7 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs367665450 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7830766,Human_RBP_ID_16402780 51782 RMVar_ID_51782 Human_SNP_ID_357742566 A-to-I Human chr8 + 30188800 30188800 30188800 ACAACTCACTGCACCCTCAACCTCCTGGGCTCAAGCAATCCTCCTGCCTCAGCCTCCTGAGAAGC ACAACTCACTGCACCCTCAACCTCCTGGGCTCCAGCAATCCTCCTGCCTCAGCCTCCTGAGAAGC A C RF00017-4490 RNACentral:URS0000922AF7 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs936346437 Functional Loss SNV dbSNP153 33..33 33 - - - 51783 RMVar_ID_51783 Human_SNP_ID_357742699 A-to-I Human chr8 - 30189427 30189427 30189427 AATCTAGGCAGGCCATGGTGGCTCATGCCTGTAATCCCAGCACGCTGGGAGGCTGAGGCAGGAGG AATCTAGGCAGGCCATGGTGGCTCATGCCTGTCATCCCAGCACGCTGGGAGGCTGAGGCAGGAGG T G lnc-MBOAT4-2 RNACentral:URS00008BAC84 lincRNA intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1563233384 Functional Loss SNV dbSNP153 33..33 33 - - - 51784 RMVar_ID_51784 Human_SNP_ID_357742776 A-to-I Human chr8 + 30189826 30189826 30189826 ATGGTAGTGGGCCCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATTCTTTGAGCCTA ATGGTAGTGGGCCCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATTCTTTGAGCCTA A G RF00017-4490 RNACentral:URS0000922AF7 SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1357407828 Functional Loss SNV dbSNP153 33..33 33 - - - 51785 RMVar_ID_51785 Human_SNP_ID_357842549 A-to-I Human chr8 - 30595673 30595673 30595673 TACATGCCACTACATCTAGCTAATTTTTTTGTATTTCTAGTAGAGATGGGGTTTCACCATGTTGC TACATGCCACTACATCTAGCTAATTTTTTTGTGTTTCTAGTAGAGATGGGGTTTCACCATGTTGC T C GTF2E2 Ensembl:ENSG00000197265 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1160900963 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_251101,RMVar_hsa_circ_104642,RMVar_hsa_circ_95657,RMVar_hsa_circ_251100 51786 RMVar_ID_51786 Human_SNP_ID_357842575 A-to-I Human chr8 - 30595769 30595769 30595769 AGAGTGCAGTGGTGCAATCTTGGCTCACTACAACCTCTGCCTCCAGGGCTCAATTCATCCTCCCA AGAGTGCAGTGGTGCAATCTTGGCTCACTACACCCTCTGCCTCCAGGGCTCAATTCATCCTCCCA T G GTF2E2 Ensembl:ENSG00000197265 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs550488504 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_251101,RMVar_hsa_circ_104642,RMVar_hsa_circ_95657,RMVar_hsa_circ_251100 51787 RMVar_ID_51787 Human_SNP_ID_357854958 A-to-I Human chr8 - 30644819 30644819 30644819 TTGAGCCAGGGAGGCGCAGGTTGTGGTGAGCTAAGATCGTGCCACTGCATTCTAGCCTGGACAAT TTGAGCCAGGGAGGCGCAGGTTGTGGTGAGCTGAGATCGTGCCACTGCATTCTAGCCTGGACAAT T C GTF2E2 Ensembl:ENSG00000197265 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1269692584 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_12531,RMVar_hsa_circ_295006,RMVar_hsa_circ_73752 51788 RMVar_ID_51788 Human_SNP_ID_357857340 A-to-I Human chr8 - 30653977 30653977 30653977 TGAAGTGATCCTCCCACTTCCGCCTCCCGAGTAGCTGGGACTGTAAGCACACATCACCATGCCTG TGAAGTGATCCTCCCACTTCCGCCTCCCGAGTGGCTGGGACTGTAAGCACACATCACCATGCCTG T C GTF2E2 Ensembl:ENSG00000197265 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1162689211 Functional Loss SNV dbSNP153 33..33 33 - - - 51789 RMVar_ID_51789 Human_SNP_ID_357857498 A-to-I Human chr8 - 30654531 30654531 30654531 GTGTGTGGTGGCGTGTACCTGTAGTACTAGCTAGTCAGGAGGCTGAGGTGGGAGGATTGCTTGAG GTGTGTGGTGGCGTGTACCTGTAGTACTAGCTGGTCAGGAGGCTGAGGTGGGAGGATTGCTTGAG T C GTF2E2 Ensembl:ENSG00000197265 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1483509978 Functional Loss SNV dbSNP153 33..33 33 - - - 51790 RMVar_ID_51790 Human_SNP_ID_357857922 A-to-I Human chr8 - 30656087 30656087 30656087 AACTGAGGCCGGGTGCGGTGACTCACGCCTGTAATCTAAGCACTTTGGGAGGCTGAGGTGGGCGG AACTGAGGCCGGGTGCGGTGACTCACGCCTGTCATCTAAGCACTTTGGGAGGCTGAGGTGGGCGG T G GTF2E2 Ensembl:ENSG00000197265 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1300700548 Functional Loss SNV dbSNP153 33..33 33 - - - 51791 RMVar_ID_51791 Human_SNP_ID_357863552 A-to-I Human chr8 - 30677151 30677151 30677151 CCTTAGAAGTAATCTGCCCACCTCGGCCTCCCAAAGTGCTGAGATTACAGGCGTGAGCCACCACA CCTTAGAAGTAATCTGCCCACCTCGGCCTCCCGAAGTGCTGAGATTACAGGCGTGAGCCACCACA T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1008575155 Functional Loss SNV dbSNP153 33..33 33 - - - 51792 RMVar_ID_51792 Human_SNP_ID_357863563 A-to-I Human chr8 - 30677173 30677173 30677173 CAGGCTGGTCTTGAACTCCTGACCTTAGAAGTAATCTGCCCACCTCGGCCTCCCAAAGTGCTGAG CAGGCTGGTCTTGAACTCCTGACCTTAGAAGTGATCTGCCCACCTCGGCCTCCCAAAGTGCTGAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1459130809 Functional Loss SNV dbSNP153 33..33 33 - - - 51793 RMVar_ID_51793 Human_SNP_ID_357863623 A-to-I Human chr8 - 30677360 30677360 30677360 ACCAAGCCTGGCTCTGTTGCCTAGGCTGGAGTACAGTGGCACGATCTCGGCTCACTGCAGCCTCT ACCAAGCCTGGCTCTGTTGCCTAGGCTGGAGTGCAGTGGCACGATCTCGGCTCACTGCAGCCTCT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1213723515 Functional Loss SNV dbSNP153 33..33 33 - - - 51794 RMVar_ID_51794 Human_SNP_ID_357863981 A-to-I Human chr8 - 30678436 30678436 30678436 GGATCACTTGAGCTTGGGTGAGGTGAGGCTGCAGTGAGTCCTGATCATGCTGCTGCACTCAATCT GGATCACTTGAGCTTGGGTGAGGTGAGGCTGCGGTGAGTCCTGATCATGCTGCTGCACTCAATCT T C GSR Ensembl:ENSG00000104687 Protein coding 3'UTR GSE38233;GSE100210;GSE112787 cultured B-cells;HepG2 cell line;293 Flip-In T-REx cells,empty vector - 24183664,29129909,29967493 RNA-Seq:(High) rs1138117 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_698508,Human_RBP_ID_7831219,Human_RBP_ID_24255463 RMVar_hsa_circ_120092,RMVar_hsa_circ_251107,RMVar_hsa_circ_91847,RMVar_hsa_circ_251106 51795 RMVar_ID_51795 Human_SNP_ID_357863987 A-to-I Human chr8 - 30678463 30678463 30678463 TCAGCTACTTGGGAGGCTGAGGTGAGAGGATCACTTGAGCTTGGGTGAGGTGAGGCTGCAGTGAG TCAGCTACTTGGGAGGCTGAGGTGAGAGGATCGCTTGAGCTTGGGTGAGGTGAGGCTGCAGTGAG T C GSR Ensembl:ENSG00000104687 Protein coding 3'UTR GSE38233;GSE100210;GSE112787 cultured B-cells;HepG2 cell line;293 Flip-In T-REx cells,empty vector - 24183664,29129909,29967493 RNA-Seq:(High) rs1138107 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7831223,Human_RBP_ID_17578620,Human_RBP_ID_26555359 RMVar_hsa_circ_120092,RMVar_hsa_circ_251107,RMVar_hsa_circ_91847,RMVar_hsa_circ_251106 51796 RMVar_ID_51796 Human_SNP_ID_357863993 A-to-I Human chr8 - 30678498 30678498 30678498 AAATTACCCGAGTGTGGTGATGTGCATCTGTAATCTCAGCTACTTGGGAGGCTGAGGTGAGAGGA AAATTACCCGAGTGTGGTGATGTGCATCTGTAGTCTCAGCTACTTGGGAGGCTGAGGTGAGAGGA T C GSR Ensembl:ENSG00000104687 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-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 51797 RMVar_ID_51797 Human_SNP_ID_357863994 A-to-I Human chr8 - 30678499 30678499 30678499 AAAATTACCCGAGTGTGGTGATGTGCATCTGTAATCTCAGCTACTTGGGAGGCTGAGGTGAGAGG AAAATTACCCGAGTGTGGTGATGTGCATCTGTGATCTCAGCTACTTGGGAGGCTGAGGTGAGAGG T C GSR Ensembl:ENSG00000104687 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-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 51798 RMVar_ID_51798 Human_SNP_ID_357863995 A-to-I Human chr8 - 30678505 30678505 30678505 GTAAAAAAAATTACCCGAGTGTGGTGATGTGCATCTGTAATCTCAGCTACTTGGGAGGCTGAGGT GTAAAAAAAATTACCCGAGTGTGGTGATGTGCGTCTGTAATCTCAGCTACTTGGGAGGCTGAGGT T C GSR Ensembl:ENSG00000104687 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs926354731 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7831224,Human_RBP_ID_16403607,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 51799 RMVar_ID_51799 Human_SNP_ID_357864014 A-to-I Human chr8 - 30678561 30678561 30678561 GCCTACAAGTTTGAGGCCAGCATGCACAGCATAGCAAGACTGCATCTCTACAGAGAGTAAAAAAA GCCTACAAGTTTGAGGCCAGCATGCACAGCATTGCAAGACTGCATCTCTACAGAGAGTAAAAAAA T A GSR Ensembl:ENSG00000104687 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs11552954 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7831226,Human_RBP_ID_23199355,Human_RBP_ID_24255465,Human_RBP_ID_24441439,Human_RBP_ID_26555360 RMVar_hsa_circ_120092,RMVar_hsa_circ_251107,RMVar_hsa_circ_91847,RMVar_hsa_circ_251106 51800 RMVar_ID_51800 Human_SNP_ID_357864015 A-to-I Human chr8 - 30678561 30678561 30678561 GCCTACAAGTTTGAGGCCAGCATGCACAGCATAGCAAGACTGCATCTCTACAGAGAGTAAAAAAA GCCTACAAGTTTGAGGCCAGCATGCACAGCATGGCAAGACTGCATCTCTACAGAGAGTAAAAAAA T C GSR Ensembl:ENSG00000104687 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs11552954 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7831226,Human_RBP_ID_23199355,Human_RBP_ID_24255465,Human_RBP_ID_24441439,Human_RBP_ID_26555360 RMVar_hsa_circ_120092,RMVar_hsa_circ_251107,RMVar_hsa_circ_91847,RMVar_hsa_circ_251106 51801 RMVar_ID_51801 Human_SNP_ID_357864034 A-to-I Human chr8 - 30678626 30678626 30678626 AAGGCACGGTGGCTCAGGCCTGTAATTCTAGCACTTTGGGAGGCCGAGGCAGGAGGATTACTTGA AAGGCACGGTGGCTCAGGCCTGTAATTCTAGCCCTTTGGGAGGCCGAGGCAGGAGGATTACTTGA T G GSR Ensembl:ENSG00000104687 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1421484082 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5224682,Human_RBP_ID_16403609,Human_RBP_ID_23199357,Human_RBP_ID_24441440,Human_RBP_ID_26555362 Human_miRNA_ID_1942296,Human_miRNA_ID_1945339,Human_miRNA_ID_2086084,Human_miRNA_ID_2116487,Human_miRNA_ID_2200061,Human_miRNA_ID_2203127,Human_miRNA_ID_2315575,Human_miRNA_ID_2318734,Human_miRNA_ID_2321892,Human_miRNA_ID_2325056,Human_miRNA_ID_2328181,Human_miRNA_ID_2519435,Human_miRNA_ID_2522598,Human_miRNA_ID_2815587,Human_miRNA_ID_2821794,Human_miRNA_ID_2827922,Human_miRNA_ID_2831078,Human_miRNA_ID_2835199,Human_miRNA_ID_2840555,Human_miRNA_ID_2845713,Human_miRNA_ID_2848733,Human_miRNA_ID_2862850,Human_miRNA_ID_3112579 RMVar_hsa_circ_120092,RMVar_hsa_circ_251107,RMVar_hsa_circ_91847,RMVar_hsa_circ_251106 51802 RMVar_ID_51802 Human_SNP_ID_357864141 A-to-I Human chr8 - 30679001 30679001 30679001 GGAATTACAGGCACGCACCACCATGCCTGACTAATTTTGTATTTTTAGTAGACATGGGGTTTCTC GGAATTACAGGCACGCACCACCATGCCTGACTGATTTTGTATTTTTAGTAGACATGGGGTTTCTC T C GSR Ensembl:ENSG00000104687 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1399323403 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26559088 RMVar_hsa_circ_120092,RMVar_hsa_circ_251107,RMVar_hsa_circ_91847,RMVar_hsa_circ_251106 51803 RMVar_ID_51803 Human_SNP_ID_357864176 A-to-I Human chr8 - 30679148 30679139 30679149 AGAACTTGCTACTTTTTTTTTTTTTTTTTTTGAGACAGAGTTTTGCTCTCATTGCCCAGGCTGGA AGAACTTGCTACTTTTTTTTTTTTTTTTTTT__________TTTGCTCTCATTGCCCAGGCTGGA AACTCTGTCTC A GSR Ensembl:ENSG00000104687 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1471583522 Functional Loss DEL dbSNP153 32..41 33 - - - Human_RBP_ID_698516,Human_RBP_ID_4982722,Human_RBP_ID_7831242,Human_RBP_ID_16403625,Human_RBP_ID_24441938 Human_miRNA_ID_1103620,Human_miRNA_ID_1530613,Human_miRNA_ID_2032164,Human_miRNA_ID_2887100 RMVar_hsa_circ_120092,RMVar_hsa_circ_251107,RMVar_hsa_circ_91847,RMVar_hsa_circ_251106 51804 RMVar_ID_51804 Human_SNP_ID_357865371 A-to-I Human chr8 - 30683665 30683665 30683665 TTTCAACCTTCCTGGGCTCAGGTGATCCTCCCACCTCAGACTCCCAAGTAGCTAGGATCACAGGT TTTCAACCTTCCTGGGCTCAGGTGATCCTCCCCCCTCAGACTCCCAAGTAGCTAGGATCACAGGT T G GSR Ensembl:ENSG00000104687 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1390176798 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_251111,RMVar_hsa_circ_120092,RMVar_hsa_circ_280524,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_21384,RMVar_hsa_circ_251109,RMVar_hsa_circ_251110,RMVar_hsa_circ_251108 51805 RMVar_ID_51805 Human_SNP_ID_357867284 A-to-I Human chr8 - 30690311 30690311 30690311 TATGAAAAATTTAAAAATTAGCCAGATGAGGTAGCACGTGCCTGTTGTCCTAGCTACCCAGGAGG TATGAAAAATTTAAAAATTAGCCAGATGAGGTGGCACGTGCCTGTTGTCCTAGCTACCCAGGAGG T C GSR Ensembl:ENSG00000104687 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1170128840 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_251111,RMVar_hsa_circ_120092,RMVar_hsa_circ_328758,RMVar_hsa_circ_251107,RMVar_hsa_circ_349297,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_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 51806 RMVar_ID_51806 Human_SNP_ID_357868324 A-to-I Human chr8 - 30694464 30694461 30694464 TACTACAAAAAATTAAAAAATTAGCAAGGTGTAGTGGTATACGCCTGTAGTTGCAGCTACTTGGG TACTACAAAAAATTAAAAAATTAGCAAGGTGT___GGTATACGCCTGTAGTTGCAGCTACTTGGG CACT C GSR Ensembl:ENSG00000104687 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1255893750 Functional Loss DEL dbSNP153 33..35 33 - - - RMVar_hsa_circ_251111,RMVar_hsa_circ_120092,RMVar_hsa_circ_328758,RMVar_hsa_circ_251107,RMVar_hsa_circ_349297,RMVar_hsa_circ_291496,RMVar_hsa_circ_289983,RMVar_hsa_circ_269450,RMVar_hsa_circ_277103,RMVar_hsa_circ_251112,RMVar_hsa_circ_99877,RMVar_hsa_circ_251114,RMVar_hsa_circ_251110,RMVar_hsa_circ_316740,RMVar_hsa_circ_361217,RMVar_hsa_circ_313640,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_290023,RMVar_hsa_circ_251118,RMVar_hsa_circ_251119,RMVar_hsa_circ_352903,RMVar_hsa_circ_377881,RMVar_hsa_circ_370787,RMVar_hsa_circ_289868,RMVar_hsa_circ_251121,RMVar_hsa_circ_251123,RMVar_hsa_circ_72275,RMVar_hsa_circ_251122,RMVar_hsa_circ_251120 51807 RMVar_ID_51807 Human_SNP_ID_357868913 A-to-I Human chr8 - 30696834 30696834 30696834 AAACTTAGCTGGGTGTGGCGATGAATGTCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCTGGAGG AAACTTAGCTGGGTGTGGCGATGAATGTCTGTGGTCCCAGCTACTCAGGAGGCTGAGGCTGGAGG T C GSR Ensembl:ENSG00000104687 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs758822288 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_251111,RMVar_hsa_circ_120092,RMVar_hsa_circ_251107,RMVar_hsa_circ_349297,RMVar_hsa_circ_291496,RMVar_hsa_circ_289983,RMVar_hsa_circ_269450,RMVar_hsa_circ_277103,RMVar_hsa_circ_251112,RMVar_hsa_circ_99877,RMVar_hsa_circ_251114,RMVar_hsa_circ_316740,RMVar_hsa_circ_361217,RMVar_hsa_circ_303087,RMVar_hsa_circ_267311,RMVar_hsa_circ_349314,RMVar_hsa_circ_251113,RMVar_hsa_circ_373280,RMVar_hsa_circ_290023,RMVar_hsa_circ_251119,RMVar_hsa_circ_352903,RMVar_hsa_circ_377881,RMVar_hsa_circ_289868,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_312483,RMVar_hsa_circ_251124 51808 RMVar_ID_51808 Human_SNP_ID_357870707 A-to-I Human chr8 - 30703496 30703496 30703496 GCTATCCACCCACCTCTGCCTCCCAAAGTGCTAGGATTACAGGTGTAAGCCACCTGTGCCCAGCC GCTATCCACCCACCTCTGCCTCCCAAAGTGCTGGGATTACAGGTGTAAGCCACCTGTGCCCAGCC T C GSR Ensembl:ENSG00000104687 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1273976175 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3155699,Human_RBP_ID_8686012 RMVar_hsa_circ_120092,RMVar_hsa_circ_251107,RMVar_hsa_circ_349297,RMVar_hsa_circ_289983,RMVar_hsa_circ_269450,RMVar_hsa_circ_99877,RMVar_hsa_circ_361217,RMVar_hsa_circ_267311,RMVar_hsa_circ_373280,RMVar_hsa_circ_251119,RMVar_hsa_circ_377881,RMVar_hsa_circ_40552,RMVar_hsa_circ_251123,RMVar_hsa_circ_72275,RMVar_hsa_circ_251122,RMVar_hsa_circ_345269,RMVar_hsa_circ_342550,RMVar_hsa_circ_251129,RMVar_hsa_circ_310833,RMVar_hsa_circ_371556,RMVar_hsa_circ_251124,RMVar_hsa_circ_340323,RMVar_hsa_circ_251125,RMVar_hsa_circ_251126,RMVar_hsa_circ_378637 51809 RMVar_ID_51809 Human_SNP_ID_357871348 A-to-I Human chr8 - 30706317 30706317 30706317 TTTTGTATTTTTAGTAGAGATAGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTAGCCT TTTTGTATTTTTAGTAGAGATAGGGTTTCACCGTGTTGGCCAGGCTGGTCTTGAACTCCTAGCCT T C GSR Ensembl:ENSG00000104687 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1025260640 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_120092,RMVar_hsa_circ_251107,RMVar_hsa_circ_349297,RMVar_hsa_circ_289983,RMVar_hsa_circ_269450,RMVar_hsa_circ_99877,RMVar_hsa_circ_361217,RMVar_hsa_circ_267311,RMVar_hsa_circ_373280,RMVar_hsa_circ_251119,RMVar_hsa_circ_377881,RMVar_hsa_circ_40552,RMVar_hsa_circ_251123,RMVar_hsa_circ_72275,RMVar_hsa_circ_251122,RMVar_hsa_circ_345269,RMVar_hsa_circ_342550,RMVar_hsa_circ_251129,RMVar_hsa_circ_310833,RMVar_hsa_circ_371556,RMVar_hsa_circ_251124,RMVar_hsa_circ_340323,RMVar_hsa_circ_251125,RMVar_hsa_circ_251126,RMVar_hsa_circ_378637 51810 RMVar_ID_51810 Human_SNP_ID_357871494 A-to-I Human chr8 - 30706952 30706952 30706952 TTTTGTATTTTTACTAGAAACGGGATTTCACCATGTTGGCCAGGGGTCTCGAACTCCTGACCTCA TTTTGTATTTTTACTAGAAACGGGATTTCACCTTGTTGGCCAGGGGTCTCGAACTCCTGACCTCA T A GSR Ensembl:ENSG00000104687 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs540149524 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16403744 RMVar_hsa_circ_120092,RMVar_hsa_circ_251107,RMVar_hsa_circ_349297,RMVar_hsa_circ_289983,RMVar_hsa_circ_269450,RMVar_hsa_circ_99877,RMVar_hsa_circ_361217,RMVar_hsa_circ_267311,RMVar_hsa_circ_373280,RMVar_hsa_circ_251119,RMVar_hsa_circ_377881,RMVar_hsa_circ_40552,RMVar_hsa_circ_251123,RMVar_hsa_circ_72275,RMVar_hsa_circ_251122,RMVar_hsa_circ_345269,RMVar_hsa_circ_342550,RMVar_hsa_circ_251129,RMVar_hsa_circ_310833,RMVar_hsa_circ_371556,RMVar_hsa_circ_251124,RMVar_hsa_circ_340323,RMVar_hsa_circ_251125,RMVar_hsa_circ_251126,RMVar_hsa_circ_378637 51811 RMVar_ID_51811 Human_SNP_ID_357871495 A-to-I Human chr8 - 30706952 30706952 30706952 TTTTGTATTTTTACTAGAAACGGGATTTCACCATGTTGGCCAGGGGTCTCGAACTCCTGACCTCA TTTTGTATTTTTACTAGAAACGGGATTTCACCGTGTTGGCCAGGGGTCTCGAACTCCTGACCTCA T C GSR Ensembl:ENSG00000104687 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs540149524 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16403744 RMVar_hsa_circ_120092,RMVar_hsa_circ_251107,RMVar_hsa_circ_349297,RMVar_hsa_circ_289983,RMVar_hsa_circ_269450,RMVar_hsa_circ_99877,RMVar_hsa_circ_361217,RMVar_hsa_circ_267311,RMVar_hsa_circ_373280,RMVar_hsa_circ_251119,RMVar_hsa_circ_377881,RMVar_hsa_circ_40552,RMVar_hsa_circ_251123,RMVar_hsa_circ_72275,RMVar_hsa_circ_251122,RMVar_hsa_circ_345269,RMVar_hsa_circ_342550,RMVar_hsa_circ_251129,RMVar_hsa_circ_310833,RMVar_hsa_circ_371556,RMVar_hsa_circ_251124,RMVar_hsa_circ_340323,RMVar_hsa_circ_251125,RMVar_hsa_circ_251126,RMVar_hsa_circ_378637 51812 RMVar_ID_51812 Human_SNP_ID_357873035 A-to-I Human chr8 - 30712546 30712546 30712546 CCTCAGCCTCCTGAGTAGCTGGGACCACAGGCATGCACCACCACACCCAGCTACTTTTTTTTGTA CCTCAGCCTCCTGAGTAGCTGGGACCACAGGCCTGCACCACCACACCCAGCTACTTTTTTTTGTA T G GSR Ensembl:ENSG00000104687 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1191984339 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_99877,RMVar_hsa_circ_251123 51813 RMVar_ID_51813 Human_SNP_ID_357884005 A-to-I Human chr8 + 30755506 30755506 30755506 CTGTTGTGGTGGCTAACGCCTGTAATCCCAGCAATTTGGAAGGATGAGGCAGGCAGATTGCTTGA CTGTTGTGGTGGCTAACGCCTGTAATCCCAGCCATTTGGAAGGATGAGGCAGGCAGATTGCTTGA A C UBXN8 Ensembl:ENSG00000104691 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1413422199 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75201,RMVar_hsa_circ_376952 51814 RMVar_ID_51814 Human_SNP_ID_357884006 A-to-I Human chr8 + 30755506 30755506 30755506 CTGTTGTGGTGGCTAACGCCTGTAATCCCAGCAATTTGGAAGGATGAGGCAGGCAGATTGCTTGA CTGTTGTGGTGGCTAACGCCTGTAATCCCAGCGATTTGGAAGGATGAGGCAGGCAGATTGCTTGA A G UBXN8 Ensembl:ENSG00000104691 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1413422199 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75201,RMVar_hsa_circ_376952 51815 RMVar_ID_51815 Human_SNP_ID_357884037 A-to-I Human chr8 + 30755622 30755622 30755622 AAAAAAAAAATTAAAAATTAGCCAGACGTGGTAGTGTGTGGCTGTAGTCTCAGCTACTTGGGAGG AAAAAAAAAATTAAAAATTAGCCAGACGTGGTGGTGTGTGGCTGTAGTCTCAGCTACTTGGGAGG A G UBXN8 Ensembl:ENSG00000104691 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1252174052 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_75201,RMVar_hsa_circ_376952 51816 RMVar_ID_51816 Human_SNP_ID_357897039 A-to-I Human chr8 - 30803350 30803350 30803350 TTTGTAGAGACAGGGTCTCCTCATGTTGTCCAAGGTGATCTTGAACTCCTGGACTCAAGTGATCC TTTGTAGAGACAGGGTCTCCTCATGTTGTCCACGGTGATCTTGAACTCCTGGACTCAAGTGATCC T G PPP2CB Ensembl:ENSG00000104695 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs750797990 Functional Loss SNV dbSNP153 33..33 33 - - - 51817 RMVar_ID_51817 Human_SNP_ID_357897631 A-to-I Human chr8 - 30805448 30805448 30805448 TCATGCCATTCACCTGCCCCAGCCTCCCGAGTAGCTGGGACTACAGGTGCCTGCCACCACTCCCG TCATGCCATTCACCTGCCCCAGCCTCCCGAGTGGCTGGGACTACAGGTGCCTGCCACCACTCCCG T C PPP2CB Ensembl:ENSG00000104695 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs945960810 Functional Loss SNV dbSNP153 33..33 33 - - - 51818 RMVar_ID_51818 Human_SNP_ID_357898805 A-to-I Human chr8 - 30809723 30809723 30809723 TTGCCCAGGCTGGTCTCGAACTCTCGGGCTCAAGTGATCCTCCCGCCTTGGCCTCCCAAAGTGCA TTGCCCAGGCTGGTCTCGAACTCTCGGGCTCAGGTGATCCTCCCGCCTTGGCCTCCCAAAGTGCA T C PPP2CB Ensembl:ENSG00000104695 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1039372085 Functional Loss SNV dbSNP153 33..33 33 - - - 51819 RMVar_ID_51819 Human_SNP_ID_357928043 A-to-I Human chr8 + 30921183 30921183 30921183 AGGAGTGCTGCCAGAAATTTGAACAACTTTCCAAATCTGCAAAAGAAGAGCTGATAAATTTCAAA AGGAGTGCTGCCAGAAATTTGAACAACTTTCCGAATCTGCAAAAGAAGAGCTGATAAATTTCAAA A G AC090281.1 Ensembl:ENSG00000253204 Pseudogene exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs879062463 Functional Loss SNV dbSNP153 33..33 33 - - - 51820 RMVar_ID_51820 Human_SNP_ID_357964857 A-to-I Human chr8 + 31071003 31071003 31071003 GGGAGGTGGAGGTTGTAGTGAGCTGAGATTGCACCATTGCACTCCAGCCTGCACAAGAGCGAGAC GGGAGGTGGAGGTTGTAGTGAGCTGAGATTGCGCCATTGCACTCCAGCCTGCACAAGAGCGAGAC A G WRN Ensembl:ENSG00000165392 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1165731739 Functional Loss SNV dbSNP153 33..33 33 - - - 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 51821 RMVar_ID_51821 Human_SNP_ID_358172274 A-to-I Human chr8 + 31904524 31904524 31904524 CAAAGAACATTTGACCTGGCAATCCTATTATTAGGTATATACCCAAAGGAGTATAAATCATTCTA CAAAGAACATTTGACCTGGCAATCCTATTATTTGGTATATACCCAAAGGAGTATAAATCATTCTA A T NRG1 Ensembl:ENSG00000157168 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs896080991 Functional Loss SNV dbSNP153 33..33 33 - - - 51822 RMVar_ID_51822 Human_SNP_ID_358173895 A-to-I Human chr8 + 31911517 31911517 31911517 CAGAAAACTAAATACCTCATGTTCTCACTTATAAGTGGGAGCGAAATGATGAGACCACATGGGCA CAGAAAACTAAATACCTCATGTTCTCACTTATTAGTGGGAGCGAAATGATGAGACCACATGGGCA A T NRG1 Ensembl:ENSG00000157168 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1276926199 Functional Loss SNV dbSNP153 33..33 33 - - - 51823 RMVar_ID_51823 Human_SNP_ID_358267068 A-to-I Human chr8 + 32292942 32292942 32292942 CCTGACCAATATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCCAGGTGTGGTGGCAC CCTGACCAATATGGTGAAACCCCGTCTCTACTGAAAATACAAAAATTAGCCAGGTGTGGTGGCAC A G NRG1 Ensembl:ENSG00000157168 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs942187789 Functional Loss SNV dbSNP153 33..33 33 - - - 51824 RMVar_ID_51824 Human_SNP_ID_358267069 A-to-I Human chr8 + 32292948 32292948 32292948 CAATATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCCAGGTGTGGTGGCACACGCCT CAATATGGTGAAACCCCGTCTCTACTAAAAATTCAAAAATTAGCCAGGTGTGGTGGCACACGCCT A T NRG1 Ensembl:ENSG00000157168 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs141715666 Functional Loss SNV dbSNP153 33..33 33 - - - GWAS_ID_6610,GWAS_ID_6611,GWAS_ID_6612,GWAS_ID_6613,GWAS_ID_6614,GWAS_ID_6615,GWAS_ID_6616 51825 RMVar_ID_51825 Human_SNP_ID_358267072 A-to-I Human chr8 + 32292961 32292961 32292961 CCCCGTCTCTACTAAAAATACAAAAATTAGCCAGGTGTGGTGGCACACGCCTTTAATCCCAGCTA CCCCGTCTCTACTAAAAATACAAAAATTAGCCCGGTGTGGTGGCACACGCCTTTAATCCCAGCTA A C NRG1 Ensembl:ENSG00000157168 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1257576018 Functional Loss SNV dbSNP153 33..33 33 - - - 51826 RMVar_ID_51826 Human_SNP_ID_358267077 A-to-I Human chr8 + 32292997 32292997 32292997 GTGGTGGCACACGCCTTTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACCTG GTGGTGGCACACGCCTTTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCTG A G NRG1 Ensembl:ENSG00000157168 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs900598474 Functional Loss SNV dbSNP153 33..33 33 - - - 51827 RMVar_ID_51827 Human_SNP_ID_358536562 A-to-I Human chr8 - 33422326 33422326 33422326 GTTGGCTAGGCTGGTCTTGAACTCCTGATCTCAGGTGATCCACCCATCTTGGCCTCCCAAAGTGC GTTGGCTAGGCTGGTCTTGAACTCCTGATCTCGGGTGATCCACCCATCTTGGCCTCCCAAAGTGC T C FUT10 Ensembl:ENSG00000172728 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1288193867 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43205 51828 RMVar_ID_51828 Human_SNP_ID_358536732 A-to-I Human chr8 - 33422954 33422954 33422954 AGAATTATCCAGGCATGGTGGTGCATGCCTGTAGTTCCAGCTACTCGGGGGGCTGAGGTGGGAGC AGAATTATCCAGGCATGGTGGTGCATGCCTGTCGTTCCAGCTACTCGGGGGGCTGAGGTGGGAGC T G FUT10 Ensembl:ENSG00000172728 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1484583838 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26168304 RMVar_hsa_circ_43205 51829 RMVar_ID_51829 Human_SNP_ID_358539733 A-to-I Human chr8 - 33435640 33435640 33435640 GTGGTGGCACACACCTGTAATCCCATCTACTCAGGTAGCCGAGGCAGGAGAATTGCATGAACCAG GTGGTGGCACACACCTGTAATCCCATCTACTCGGGTAGCCGAGGCAGGAGAATTGCATGAACCAG T C FUT10 Ensembl:ENSG00000172728 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1312387900 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43205 51830 RMVar_ID_51830 Human_SNP_ID_358541475 A-to-I Human chr8 - 33442686 33442686 33442686 GGAGGCCAAGGCGGGCAGATTGCTTGAGCCCAAGAGTTCGAGACCAGCCTGAGCAATACAGAGAG GGAGGCCAAGGCGGGCAGATTGCTTGAGCCCAGGAGTTCGAGACCAGCCTGAGCAATACAGAGAG T C FUT10 Ensembl:ENSG00000172728 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs891443992 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_43205 51831 RMVar_ID_51831 Human_SNP_ID_358549148 A-to-I Human chr8 - 33473555 33473553 33473555 ACTCTGCTAATTTTTGCATTTTTTGTAGAGACAGGGTCCCGCTATGTTGCTCAGGCTGGTATCGA ACTCTGCTAATTTTTGCATTTTTTGTAGAGAC__GGTCCCGCTATGTTGCTCAGGCTGGTATCGA CCT C TTI2 Ensembl:ENSG00000129696 Protein coding exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1285520771 Functional Loss DEL dbSNP153 33..34 33 - - - 51832 RMVar_ID_51832 Human_SNP_ID_358555111 A-to-I Human chr8 + 33497512 33497512 33497512 CATCTCTAATAAAAAAAAAAATTTTTTTTTTTAGATGAAGTTTCGCTCTGTAGCTCAGGCTAGAG CATCTCTAATAAAAAAAAAAATTTTTTTTTTTGGATGAAGTTTCGCTCTGTAGCTCAGGCTAGAG A G MAK16 Ensembl:ENSG00000198042 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1421889894 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86342,RMVar_hsa_circ_251234 51833 RMVar_ID_51833 Human_SNP_ID_358555171 A-to-I Human chr8 + 33497746 33497746 33497746 GAACTCCAGACCTCTGGTAATCCGCCTGCCTCAGTCTCCCAAAGTGCTAAGATTAGAGGCATGAG GAACTCCAGACCTCTGGTAATCCGCCTGCCTCGGTCTCCCAAAGTGCTAAGATTAGAGGCATGAG A G MAK16 Ensembl:ENSG00000198042 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1269121385 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86342,RMVar_hsa_circ_251234 51834 RMVar_ID_51834 Human_SNP_ID_358555172 A-to-I Human chr8 + 33497746 33497746 33497746 GAACTCCAGACCTCTGGTAATCCGCCTGCCTCAGTCTCCCAAAGTGCTAAGATTAGAGGCATGAG GAACTCCAGACCTCTGGTAATCCGCCTGCCTCTGTCTCCCAAAGTGCTAAGATTAGAGGCATGAG A T MAK16 Ensembl:ENSG00000198042 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1269121385 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86342,RMVar_hsa_circ_251234 51835 RMVar_ID_51835 Human_SNP_ID_359627328 A-to-I Human chr8 + 37747531 37747531 37747531 ATCTCCTCTTCCTCTTCATCAATGGTAGACACAGTGACAGAACTGAACTTGCCCATGTCTTTGGT ATCTCCTCTTCCTCTTCATCAATGGTAGACACGGTGACAGAACTGAACTTGCCCATGTCTTTGGT A G ERLIN2 Ensembl:ENSG00000147475 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879010644 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_34493 51836 RMVar_ID_51836 Human_SNP_ID_359629630 A-to-I Human chr8 - 37756577 37756577 37756577 ACCATTGGATTGACACTAATGTGTAGGATAACATATTTTTTGTTTAAAGAGGAAATGATAGAAAC ACCATTGGATTGACACTAATGTGTAGGATAACGTATTTTTTGTTTAAAGAGGAAATGATAGAAAC T C lnc-BRF2-2 RNACentral:URS0000D5AC6D lincRNA exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs568297308 Functional Loss SNV dbSNP153 33..33 33 - - - 51837 RMVar_ID_51837 Human_SNP_ID_359629631 A-to-I Human chr8 - 37756577 37756577 37756577 ACCATTGGATTGACACTAATGTGTAGGATAACATATTTTTTGTTTAAAGAGGAAATGATAGAAAC ACCATTGGATTGACACTAATGTGTAGGATAACCTATTTTTTGTTTAAAGAGGAAATGATAGAAAC T G lnc-BRF2-2 RNACentral:URS0000D5AC6D lincRNA exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository - 30559470 RNA-Seq:(High) rs568297308 Functional Loss SNV dbSNP153 33..33 33 - - - 51838 RMVar_ID_51838 Human_SNP_ID_359631581 A-to-I Human chr8 + 37764353 37764353 37764353 TTGTTTTTTGTTTTATTTTGAGACGGAGTCTCACTCTGTCACCCAGGCTGGAGTGCAATGGCACA TTGTTTTTTGTTTTATTTTGAGACGGAGTCTCGCTCTGTCACCCAGGCTGGAGTGCAATGGCACA A G PLPBP Ensembl:ENSG00000147471 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1261336366 Functional Loss SNV dbSNP153 33..33 33 - - - 51839 RMVar_ID_51839 Human_SNP_ID_359631709 A-to-I Human chr8 + 37764915 37764915 37764915 ATTCTCCGCTGGGCACAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAAGTGGGCAG ATTCTCCGCTGGGCACAGTGGCTCATGCCTGTGATCCCAGCACTTTGGGAGGCCGAAGTGGGCAG A G PLPBP Ensembl:ENSG00000147471 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1294232521 Functional Loss SNV dbSNP153 33..33 33 - - - 51840 RMVar_ID_51840 Human_SNP_ID_359631745 A-to-I Human chr8 + 37765103 37765103 37765103 GAGGCAGGAGAATTGCTTGATCACTTGAACCCAGGAGGCAGAGGTTGCGGTGAGCCGAGATGGCA GAGGCAGGAGAATTGCTTGATCACTTGAACCCCGGAGGCAGAGGTTGCGGTGAGCCGAGATGGCA A C PLPBP Ensembl:ENSG00000147471 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs957532531 Functional Loss SNV dbSNP153 33..33 33 - - - 51841 RMVar_ID_51841 Human_SNP_ID_359634718 A-to-I Human chr8 + 37776853 37776853 37776853 CAGTGGCGCGATCTCAGCTCACTGTAACCTCCACCTCCCAGGTTCAAGTGATTCTCCTGCTTCAG CAGTGGCGCGATCTCAGCTCACTGTAACCTCCGCCTCCCAGGTTCAAGTGATTCTCCTGCTTCAG A G PLPBP Ensembl:ENSG00000147471 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1386285423 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_251305,RMVar_hsa_circ_113627,RMVar_hsa_circ_90934,RMVar_hsa_circ_251304,RMVar_hsa_circ_251311,RMVar_hsa_circ_95255,RMVar_hsa_circ_251313 51842 RMVar_ID_51842 Human_SNP_ID_359634722 A-to-I Human chr8 + 37776860 37776859 37776860 GCGATCTCAGCTCACTGTAACCTCCACCTCCCAGGTTCAAGTGATTCTCCTGCTTCAGCCTCCCA GCGATCTCAGCTCACTGTAACCTCCACCTCCC_GGTTCAAGTGATTCTCCTGCTTCAGCCTCCCA CA C PLPBP Ensembl:ENSG00000147471 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1302062810 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_251305,RMVar_hsa_circ_113627,RMVar_hsa_circ_90934,RMVar_hsa_circ_251304,RMVar_hsa_circ_251311,RMVar_hsa_circ_95255,RMVar_hsa_circ_251313 51843 RMVar_ID_51843 Human_SNP_ID_359634724 A-to-I Human chr8 + 37776866 37776866 37776866 TCAGCTCACTGTAACCTCCACCTCCCAGGTTCAAGTGATTCTCCTGCTTCAGCCTCCCAAGTAGC TCAGCTCACTGTAACCTCCACCTCCCAGGTTCGAGTGATTCTCCTGCTTCAGCCTCCCAAGTAGC A G PLPBP Ensembl:ENSG00000147471 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1179157810 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_251305,RMVar_hsa_circ_113627,RMVar_hsa_circ_90934,RMVar_hsa_circ_251304,RMVar_hsa_circ_251311,RMVar_hsa_circ_95255,RMVar_hsa_circ_251313 51844 RMVar_ID_51844 Human_SNP_ID_359658914 A-to-I Human chr8 - 37865457 37865457 37865457 AAATTAGCTGGATGTGGTGGCAGGTGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAA AAATTAGCTGGATGTGGTGGCAGGTGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAA T C RAB11FIP1 Ensembl:ENSG00000156675 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1563364891 Functional Loss SNV dbSNP153 33..33 33 - - - 51845 RMVar_ID_51845 Human_SNP_ID_359662768 A-to-I Human chr8 - 37878902 37878902 37878902 GCAATTATAGCTCACTGCAGCCTCGAATTCCTAGGCTCATGTTGAGTAGCTGAGAGTATAGGCGC GCAATTATAGCTCACTGCAGCCTCGAATTCCTTGGCTCATGTTGAGTAGCTGAGAGTATAGGCGC T A RAB11FIP1 Ensembl:ENSG00000156675 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs545607681 Functional Loss SNV dbSNP153 33..33 33 - - - 51846 RMVar_ID_51846 Human_SNP_ID_359662769 A-to-I Human chr8 - 37878902 37878902 37878902 GCAATTATAGCTCACTGCAGCCTCGAATTCCTAGGCTCATGTTGAGTAGCTGAGAGTATAGGCGC GCAATTATAGCTCACTGCAGCCTCGAATTCCTGGGCTCATGTTGAGTAGCTGAGAGTATAGGCGC T C RAB11FIP1 Ensembl:ENSG00000156675 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs545607681 Functional Loss SNV dbSNP153 33..33 33 - - - 51847 RMVar_ID_51847 Human_SNP_ID_359664646 A-to-I Human chr8 - 37887462 37887462 37887462 CCGTGGCGCGATCTTGGCTCACTGCAACCTCCACTTTCCAGGTTCAAGCAATTCTTGTGCCTCAT CCGTGGCGCGATCTTGGCTCACTGCAACCTCCGCTTTCCAGGTTCAAGCAATTCTTGTGCCTCAT T C RAB11FIP1 Ensembl:ENSG00000156675 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1261485296 Functional Loss SNV dbSNP153 33..33 33 - - - 51848 RMVar_ID_51848 Human_SNP_ID_359708662 A-to-I Human chr8 + 38061115 38061115 38061115 AAGTTTTTTGTGAGTAGAGATAAGGTCTTGCTATGTTGCCCAGGCTGGTCTTGAACTCCTGGTCT AAGTTTTTTGTGAGTAGAGATAAGGTCTTGCTCTGTTGCCCAGGCTGGTCTTGAACTCCTGGTCT A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355040240 Functional Loss SNV dbSNP153 33..33 33 - - - 51849 RMVar_ID_51849 Human_SNP_ID_359709571 A-to-I Human chr8 + 38064905 38064905 38064905 GCTGGAGTGCAGTGCCACAATCCCGGCTCACTACAACCTCTGCTGCCCTGGTTCAAACAATTCTC GCTGGAGTGCAGTGCCACAATCCCGGCTCACTGCAACCTCTGCTGCCCTGGTTCAAACAATTCTC A G RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1000975981 Functional Loss SNV dbSNP153 33..33 33 - - - 51850 RMVar_ID_51850 Human_SNP_ID_359709607 A-to-I Human chr8 + 38065062 38065062 38065062 GTTGACCTGGCTGGTCTCGAACTCCCAGCTTCAAGTGATCACTGCCCTCATCAGCCTCCCAAAGT GTTGACCTGGCTGGTCTCGAACTCCCAGCTTCTAGTGATCACTGCCCTCATCAGCCTCCCAAAGT A T RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs181110730 Functional Loss SNV dbSNP153 33..33 33 - - - 51851 RMVar_ID_51851 Human_SNP_ID_359720188 A-to-I Human chr8 - 38103315 38103315 38103315 TAGAGACAGGGTCTCATCATGTTGCTCAGACTAGTCTCCAACTCCCGAGCTCAAGCGATCCTCTT TAGAGACAGGGTCTCATCATGTTGCTCAGACTGGTCTCCAACTCCCGAGCTCAAGCGATCCTCTT T C RF00017-4487,RF00017-4503,lnc-STAR-1,RF00017-4596,RF00017-4544 RNACentral:URS000095255B,RNACentral:URS0000948B80,RNACentral:URS0000D5CD1B,RNACentral:URS0000934741,RNACentral:URS000093B8FA SRP RNA,SRP RNA,lincRNA,SRP RNA,SRP RNA intron,intron,exon,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917030979 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23199451 51852 RMVar_ID_51852 Human_SNP_ID_359720196 A-to-I Human chr8 - 38103340 38103340 38103340 CCCAGCTAATTTTCTTAATTTTTAGTAGAGACAGGGTCTCATCATGTTGCTCAGACTAGTCTCCA CCCAGCTAATTTTCTTAATTTTTAGTAGAGACGGGGTCTCATCATGTTGCTCAGACTAGTCTCCA T C RF00017-4487,RF00017-4503,lnc-STAR-1,RF00017-4596,RF00017-4544 RNACentral:URS000095255B,RNACentral:URS0000948B80,RNACentral:URS0000D5CD1B,RNACentral:URS0000934741,RNACentral:URS000093B8FA SRP RNA,SRP RNA,lincRNA,SRP RNA,SRP RNA intron,intron,exon,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs914657866 Functional Loss SNV dbSNP153 33..33 33 - - - 51853 RMVar_ID_51853 Human_SNP_ID_359720415 A-to-I Human chr8 - 38103995 38103995 38103995 GTCGCCCAGGCTGAGTGCAGTAGCGCGATCTCAGCTCACTGCAACCTCCACCTCGCGGTTTCGGG GTCGCCCAGGCTGAGTGCAGTAGCGCGATCTCGGCTCACTGCAACCTCCACCTCGCGGTTTCGGG 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 GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232246088 Functional Loss SNV dbSNP153 33..33 33 - - - 51854 RMVar_ID_51854 Human_SNP_ID_359720493 A-to-I Human chr8 - 38104263 38104263 38104263 GCCCGATCACGGCTCACTGCAACCTCCACCCCAGGTTCAAGCGATTCTCCTACCTCAGCCTCCCG GCCCGATCACGGCTCACTGCAACCTCCACCCCGGGTTCAAGCGATTCTCCTACCTCAGCCTCCCG 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 GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1295860737 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16410354 51855 RMVar_ID_51855 Human_SNP_ID_359730129 A-to-I Human chr8 + 38140534 38140534 38140534 AAAATTAGCCAGACGTGATGACACATGCCAGTAGTCCCAGCTACTCTGGAGGCTTAGGTGGGAGG AAAATTAGCCAGACGTGATGACACATGCCAGTTGTCCCAGCTACTCTGGAGGCTTAGGTGGGAGG A T ASH2L Ensembl:ENSG00000129691 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1226772941 Functional Loss SNV dbSNP153 33..33 33 - - - 51856 RMVar_ID_51856 Human_SNP_ID_359730146 A-to-I Human chr8 + 38140596 38140596 38140596 AGGATCCCTTGGGCCCAGGAGTTCGAGGCTGCAGTGAGCCATGTTTGCACCACAGCACTCCAGCT AGGATCCCTTGGGCCCAGGAGTTCGAGGCTGCTGTGAGCCATGTTTGCACCACAGCACTCCAGCT A T ASH2L Ensembl:ENSG00000129691 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1169700839 Functional Loss SNV dbSNP153 33..33 33 - - - 51857 RMVar_ID_51857 Human_SNP_ID_359730263 A-to-I Human chr8 + 38141000 38141000 38141000 TGACCTCATGATCTGCCCACCTCGGCTTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCACAC TGACCTCATGATCTGCCCACCTCGGCTTCCCAGAGTGCTGGGATTACAGGCATGAGCCACCACAC A G ASH2L Ensembl:ENSG00000129691 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs181364550 Functional Loss SNV dbSNP153 33..33 33 - - - 51858 RMVar_ID_51858 Human_SNP_ID_359739286 A-to-I Human chr8 - 38172504 38172504 38172504 CAGCCTAGCTAACATGGTGATACACCATCTCTACTAAAAATATGAAAATTAGCCAGGCATGGTGG CAGCCTAGCTAACATGGTGATACACCATCTCTGCTAAAAATATGAAAATTAGCCAGGCATGGTGG T C LSM1 Ensembl:ENSG00000175324 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs941566454 Functional Loss SNV dbSNP153 33..33 33 - - - 51859 RMVar_ID_51859 Human_SNP_ID_359739827 A-to-I Human chr8 - 38174912 38174912 38174912 TTAAACAATTCTTGTGCCTCAGCCTCCCAAGTAACTGGGATTACAGGCGCCTGCCAGCACGCCCA TTAAACAATTCTTGTGCCTCAGCCTCCCAAGTTACTGGGATTACAGGCGCCTGCCAGCACGCCCA T A LSM1 Ensembl:ENSG00000175324 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs894940480 Functional Loss SNV dbSNP153 33..33 33 - - - 51860 RMVar_ID_51860 Human_SNP_ID_359743953 A-to-I Human chr8 + 38189057 38189052 38189058 CTCAGTTCACTACACCTCTGCTTCCTGGGTTCAAGCAATTCTCGTGCCTCAGCCTCCTGAGTAGC CTCAGTTCACTACACCTCTGCTTCCTGG______GCAATTCTCGTGCCTCAGCCTCCTGAGTAGC GGTTCAA G BAG4 Ensembl:ENSG00000156735 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs911394798 Functional Loss DEL dbSNP153 29..34 33 - - - RMVar_hsa_circ_251365,RMVar_hsa_circ_112352 51861 RMVar_ID_51861 Human_SNP_ID_359751063 A-to-I Human chr8 + 38216639 38216639 38216639 GTGATCTCAGCTCACTGCAACCTCCAACTCCCAGGTTCAAGCAATTCTCCTGCCTTGGACTCCCG GTGATCTCAGCTCACTGCAACCTCCAACTCCCGGGTTCAAGCAATTCTCCTGCCTTGGACTCCCG A G RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1356028352 Functional Loss SNV dbSNP153 33..33 33 - - - 51862 RMVar_ID_51862 Human_SNP_ID_359751228 A-to-I Human chr8 + 38217257 38217257 38217257 TTGGGAGGCCGAGGCGGGTGGATTATGAGGTCAGGGGTTCGAGACCAGCCTGGCCAACATGGTGA TTGGGAGGCCGAGGCGGGTGGATTATGAGGTCGGGGGTTCGAGACCAGCCTGGCCAACATGGTGA A G RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1432954849 Functional Loss SNV dbSNP153 33..33 33 - - - 51863 RMVar_ID_51863 Human_SNP_ID_359751322 A-to-I Human chr8 + 38217596 38217596 38217596 CCTGCCTCAGTCTCCAAAAGTGTTAGGATTACAGACATGAACCACTGCGCCTGGCCCTATCATAT CCTGCCTCAGTCTCCAAAAGTGTTAGGATTACGGACATGAACCACTGCGCCTGGCCCTATCATAT A G RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1458397342 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16410979 51864 RMVar_ID_51864 Human_SNP_ID_359752063 A-to-I Human chr8 + 38220622 38220622 38220622 GAGTTTCGCTCTTGTTGCCCAGGCTGGAGTGCAATGGCACGATCTCGGCTCACCACAACCTCCGT GAGTTTCGCTCTTGTTGCCCAGGCTGGAGTGCGATGGCACGATCTCGGCTCACCACAACCTCCGT A G RF00017-4495 RNACentral:URS0000923EDC SRP RNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1362881865 Functional Loss SNV dbSNP153 33..33 33 - - - 51865 RMVar_ID_51865 Human_SNP_ID_359753183 A-to-I Human chr8 + 38225663 38225663 38225663 TACTCAGCTCGGCCTCCCAAAGTGTTGGGATTACAGGCATGAGCCACCACACCCAGCCTGTATGT TACTCAGCTCGGCCTCCCAAAGTGTTGGGATTGCAGGCATGAGCCACCACACCCAGCCTGTATGT A G DDHD2 Ensembl:ENSG00000085788 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1015587611 Functional Loss SNV dbSNP153 33..33 33 - - - 51866 RMVar_ID_51866 Human_SNP_ID_359755603 A-to-I Human chr8 + 38235678 38235678 38235678 GGGAGGTGGAGGTTGTGGTGAGTGGAGATCGCACCATTGAACTACAGCCTGGGCAACGAGCAAAA GGGAGGTGGAGGTTGTGGTGAGTGGAGATCGCGCCATTGAACTACAGCCTGGGCAACGAGCAAAA A G DDHD2 Ensembl:ENSG00000085788 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1289732698 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_127338,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 51867 RMVar_ID_51867 Human_SNP_ID_359757260 A-to-I Human chr8 + 38241875 38241874 38241875 CAGGAGTTCAGGACCAGCCTGGCCAACAGGACAAAACCCCATCTGTACTAAAAATACAAAAATTA CAGGAGTTCAGGACCAGCCTGGCCAACAGGAC_AAACCCCATCTGTACTAAAAATACAAAAATTA CA C DDHD2 Ensembl:ENSG00000085788 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1249552013 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_2044,RMVar_hsa_circ_343422,RMVar_hsa_circ_64088,RMVar_hsa_circ_49043,RMVar_hsa_circ_342677,RMVar_hsa_circ_49606,RMVar_hsa_circ_49346,RMVar_hsa_circ_54907,RMVar_hsa_circ_25968,RMVar_hsa_circ_362689,RMVar_hsa_circ_373005,RMVar_hsa_circ_32097,RMVar_hsa_circ_335477,RMVar_hsa_circ_32066,RMVar_hsa_circ_251371,RMVar_hsa_circ_251372 51868 RMVar_ID_51868 Human_SNP_ID_359757841 A-to-I Human chr8 + 38244508 38244508 38244508 CTGGACTCCTGACCTCATGATCTGCCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG CTGGACTCCTGACCTCATGATCTGCCCGCCTCTGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG A T DDHD2 Ensembl:ENSG00000085788 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1297275006 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_2044,RMVar_hsa_circ_64088,RMVar_hsa_circ_49043,RMVar_hsa_circ_342677,RMVar_hsa_circ_49606,RMVar_hsa_circ_54907,RMVar_hsa_circ_25968,RMVar_hsa_circ_362689,RMVar_hsa_circ_373005,RMVar_hsa_circ_32097,RMVar_hsa_circ_335477,RMVar_hsa_circ_32066,RMVar_hsa_circ_251373,RMVar_hsa_circ_316384,RMVar_hsa_circ_251371,RMVar_hsa_circ_251372,RMVar_hsa_circ_343295,RMVar_hsa_circ_355742,RMVar_hsa_circ_16746,RMVar_hsa_circ_297010,RMVar_hsa_circ_251375,RMVar_hsa_circ_251376,RMVar_hsa_circ_251374 51869 RMVar_ID_51869 Human_SNP_ID_359757922 A-to-I Human chr8 + 38244816 38244816 38244816 TCGAACTTTGGACCTCGTGATCTGCCCGCCTCAGCCTCCCAAAGTGCTGGCATTACAGGCGTGAG TCGAACTTTGGACCTCGTGATCTGCCCGCCTCGGCCTCCCAAAGTGCTGGCATTACAGGCGTGAG A G DDHD2 Ensembl:ENSG00000085788 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs900297610 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16411055 RMVar_hsa_circ_2044,RMVar_hsa_circ_64088,RMVar_hsa_circ_49043,RMVar_hsa_circ_342677,RMVar_hsa_circ_49606,RMVar_hsa_circ_54907,RMVar_hsa_circ_25968,RMVar_hsa_circ_362689,RMVar_hsa_circ_373005,RMVar_hsa_circ_32097,RMVar_hsa_circ_335477,RMVar_hsa_circ_32066,RMVar_hsa_circ_251373,RMVar_hsa_circ_316384,RMVar_hsa_circ_251371,RMVar_hsa_circ_251372,RMVar_hsa_circ_343295,RMVar_hsa_circ_355742,RMVar_hsa_circ_16746,RMVar_hsa_circ_297010,RMVar_hsa_circ_251375,RMVar_hsa_circ_251376,RMVar_hsa_circ_251374 51870 RMVar_ID_51870 Human_SNP_ID_359758341 A-to-I Human chr8 + 38246601 38246601 38246601 CGGTGGCTCATGCCTGTAATCTCAGCACTTTGAGAGGCTGAGACTGGTGGATCACCTTAGGTCAG CGGTGGCTCATGCCTGTAATCTCAGCACTTTGGGAGGCTGAGACTGGTGGATCACCTTAGGTCAG A G DDHD2 Ensembl:ENSG00000085788 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1030945063 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64088,RMVar_hsa_circ_49043,RMVar_hsa_circ_342677,RMVar_hsa_circ_49606,RMVar_hsa_circ_54907,RMVar_hsa_circ_25968,RMVar_hsa_circ_362689,RMVar_hsa_circ_373005,RMVar_hsa_circ_32097,RMVar_hsa_circ_335477,RMVar_hsa_circ_32066,RMVar_hsa_circ_251378,RMVar_hsa_circ_251373,RMVar_hsa_circ_316384,RMVar_hsa_circ_251371,RMVar_hsa_circ_251372,RMVar_hsa_circ_343295,RMVar_hsa_circ_355742,RMVar_hsa_circ_297010,RMVar_hsa_circ_251375,RMVar_hsa_circ_251376,RMVar_hsa_circ_251374,RMVar_hsa_circ_2853,RMVar_hsa_circ_368717,RMVar_hsa_circ_269712,RMVar_hsa_circ_331524,RMVar_hsa_circ_363838,RMVar_hsa_circ_16597,RMVar_hsa_circ_251377 51871 RMVar_ID_51871 Human_SNP_ID_359758348 A-to-I Human chr8 + 38246627 38246627 38246627 ACTTTGAGAGGCTGAGACTGGTGGATCACCTTAGGTCAGGAGTTCAAGACCAGCTTGGCCAACAT ACTTTGAGAGGCTGAGACTGGTGGATCACCTTGGGTCAGGAGTTCAAGACCAGCTTGGCCAACAT A G DDHD2 Ensembl:ENSG00000085788 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1238818748 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64088,RMVar_hsa_circ_49043,RMVar_hsa_circ_342677,RMVar_hsa_circ_49606,RMVar_hsa_circ_54907,RMVar_hsa_circ_25968,RMVar_hsa_circ_362689,RMVar_hsa_circ_373005,RMVar_hsa_circ_32097,RMVar_hsa_circ_335477,RMVar_hsa_circ_32066,RMVar_hsa_circ_251378,RMVar_hsa_circ_251373,RMVar_hsa_circ_316384,RMVar_hsa_circ_251371,RMVar_hsa_circ_251372,RMVar_hsa_circ_343295,RMVar_hsa_circ_355742,RMVar_hsa_circ_297010,RMVar_hsa_circ_251375,RMVar_hsa_circ_251376,RMVar_hsa_circ_251374,RMVar_hsa_circ_2853,RMVar_hsa_circ_368717,RMVar_hsa_circ_269712,RMVar_hsa_circ_331524,RMVar_hsa_circ_363838,RMVar_hsa_circ_16597,RMVar_hsa_circ_251377 51872 RMVar_ID_51872 Human_SNP_ID_359758552 A-to-I Human chr8 + 38247304 38247304 38247304 GGCGCATGCCACCGTACCCGGCTAATTTTTGTATCTTTAGTAGAGACAGGGTGTTGGTCAGACTG GGCGCATGCCACCGTACCCGGCTAATTTTTGTGTCTTTAGTAGAGACAGGGTGTTGGTCAGACTG A G DDHD2 Ensembl:ENSG00000085788 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs539170930 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64088,RMVar_hsa_circ_49043,RMVar_hsa_circ_342677,RMVar_hsa_circ_49606,RMVar_hsa_circ_54907,RMVar_hsa_circ_25968,RMVar_hsa_circ_362689,RMVar_hsa_circ_373005,RMVar_hsa_circ_32097,RMVar_hsa_circ_335477,RMVar_hsa_circ_32066,RMVar_hsa_circ_251378,RMVar_hsa_circ_251373,RMVar_hsa_circ_316384,RMVar_hsa_circ_251371,RMVar_hsa_circ_251372,RMVar_hsa_circ_343295,RMVar_hsa_circ_355742,RMVar_hsa_circ_297010,RMVar_hsa_circ_251375,RMVar_hsa_circ_251376,RMVar_hsa_circ_251374,RMVar_hsa_circ_2853,RMVar_hsa_circ_368717,RMVar_hsa_circ_269712,RMVar_hsa_circ_331524,RMVar_hsa_circ_363838,RMVar_hsa_circ_16597,RMVar_hsa_circ_251377 51873 RMVar_ID_51873 Human_SNP_ID_359758787 A-to-I Human chr8 + 38248304 38248304 38248304 AGGCTGGTCTGGAATTCCTGACCCCGTGATCCACCCACCTTGGCCTCCCAAAGTGCTGGGATTAC AGGCTGGTCTGGAATTCCTGACCCCGTGATCCCCCCACCTTGGCCTCCCAAAGTGCTGGGATTAC A C DDHD2 Ensembl:ENSG00000085788 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1269251380 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64088,RMVar_hsa_circ_49043,RMVar_hsa_circ_342677,RMVar_hsa_circ_49606,RMVar_hsa_circ_54907,RMVar_hsa_circ_25968,RMVar_hsa_circ_373005,RMVar_hsa_circ_32097,RMVar_hsa_circ_335477,RMVar_hsa_circ_32066,RMVar_hsa_circ_251378,RMVar_hsa_circ_251373,RMVar_hsa_circ_316384,RMVar_hsa_circ_251371,RMVar_hsa_circ_251372,RMVar_hsa_circ_355742,RMVar_hsa_circ_297010,RMVar_hsa_circ_251375,RMVar_hsa_circ_251376,RMVar_hsa_circ_251374,RMVar_hsa_circ_2853,RMVar_hsa_circ_368717,RMVar_hsa_circ_269712,RMVar_hsa_circ_331524,RMVar_hsa_circ_363838,RMVar_hsa_circ_16597,RMVar_hsa_circ_251380,RMVar_hsa_circ_266533,RMVar_hsa_circ_286303,RMVar_hsa_circ_351860,RMVar_hsa_circ_251377,RMVar_hsa_circ_365996,RMVar_hsa_circ_305181,RMVar_hsa_circ_283757,RMVar_hsa_circ_251382,RMVar_hsa_circ_251383,RMVar_hsa_circ_251381,RMVar_hsa_circ_251379 51874 RMVar_ID_51874 Human_SNP_ID_359760286 A-to-I Human chr8 + 38253898 38253898 38253898 GTTCAGGAGTTTGAGACCGGCCTGGGAAACATAGCAAGACCTCATCTCTACAAAAACTAAATTAG GTTCAGGAGTTTGAGACCGGCCTGGGAAACATGGCAAGACCTCATCTCTACAAAAACTAAATTAG A G DDHD2 Ensembl:ENSG00000085788 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1420058168 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64088,RMVar_hsa_circ_49043,RMVar_hsa_circ_335477,RMVar_hsa_circ_251378,RMVar_hsa_circ_251372,RMVar_hsa_circ_297010,RMVar_hsa_circ_251375,RMVar_hsa_circ_251376,RMVar_hsa_circ_251374,RMVar_hsa_circ_269712,RMVar_hsa_circ_331524,RMVar_hsa_circ_251380,RMVar_hsa_circ_266533,RMVar_hsa_circ_251377,RMVar_hsa_circ_283757,RMVar_hsa_circ_251381,RMVar_hsa_circ_251379,RMVar_hsa_circ_251386,RMVar_hsa_circ_251391,RMVar_hsa_circ_251394 51875 RMVar_ID_51875 Human_SNP_ID_359762739 A-to-I Human chr8 - 38265100 38265100 38265100 CACCACGCCCGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACTTGTTGGTCAGGCTGGT CACCACGCCCGGCTAATTTTTGTATTTTTAGTGGAGACAGGGTTTCACTTGTTGGTCAGGCTGGT T C PLPP5 Ensembl:ENSG00000147535 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs558154383 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124664,RMVar_hsa_circ_127594,RMVar_hsa_circ_251396,RMVar_hsa_circ_92211,RMVar_hsa_circ_251397,RMVar_hsa_circ_251398 51876 RMVar_ID_51876 Human_SNP_ID_359762821 A-to-I Human chr8 - 38265458 38265458 38265458 TGAAACGCTATCTCTACTAAAAATACAAAATCAGCTGGGCATGGTGGCACACGCCTTTAATCCCA TGAAACGCTATCTCTACTAAAAATACAAAATCGGCTGGGCATGGTGGCACACGCCTTTAATCCCA T C PLPP5 Ensembl:ENSG00000147535 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs931034893 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124664,RMVar_hsa_circ_127594,RMVar_hsa_circ_251396,RMVar_hsa_circ_92211,RMVar_hsa_circ_251397,RMVar_hsa_circ_251398 51877 RMVar_ID_51877 Human_SNP_ID_359762826 A-to-I Human chr8 - 38265481 38265481 38265481 TTGAAGACCAGCCTGACCAACAGTGAAACGCTATCTCTACTAAAAATACAAAATCAGCTGGGCAT TTGAAGACCAGCCTGACCAACAGTGAAACGCTCTCTCTACTAAAAATACAAAATCAGCTGGGCAT T G PLPP5 Ensembl:ENSG00000147535 Protein coding intron GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs758849368 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_124664,RMVar_hsa_circ_127594,RMVar_hsa_circ_251396,RMVar_hsa_circ_92211,RMVar_hsa_circ_251397,RMVar_hsa_circ_251398 51878 RMVar_ID_51878 Human_SNP_ID_359771091 A-to-I Human chr8 - 38301062 38301062 38301062 GGGAGGTTGAGGTGGTAGGATCACTCGAGCCCAGGAGGTTGAGGCTGCAGTGAGCTGTGATCTGC GGGAGGTTGAGGTGGTAGGATCACTCGAGCCCGGGAGGTTGAGGCTGCAGTGAGCTGTGATCTGC T C NSD3 Ensembl:ENSG00000147548 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1479083806 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267769,RMVar_hsa_circ_37839,RMVar_hsa_circ_7392,RMVar_hsa_circ_18206,RMVar_hsa_circ_268860,RMVar_hsa_circ_118503,RMVar_hsa_circ_323712,RMVar_hsa_circ_45424,RMVar_hsa_circ_251404,RMVar_hsa_circ_251405,RMVar_hsa_circ_265821,RMVar_hsa_circ_67504,RMVar_hsa_circ_11369,RMVar_hsa_circ_360614,RMVar_hsa_circ_353349 51879 RMVar_ID_51879 Human_SNP_ID_359771102 A-to-I Human chr8 - 38301108 38301108 38301108 AAACGTAGCCAGGCATGGGGACAAATGGCTGTAGTCCTAGCTACTCGGGAGGTTGAGGTGGTAGG AAACGTAGCCAGGCATGGGGACAAATGGCTGTGGTCCTAGCTACTCGGGAGGTTGAGGTGGTAGG T C NSD3 Ensembl:ENSG00000147548 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1405730977 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267769,RMVar_hsa_circ_37839,RMVar_hsa_circ_7392,RMVar_hsa_circ_18206,RMVar_hsa_circ_268860,RMVar_hsa_circ_118503,RMVar_hsa_circ_323712,RMVar_hsa_circ_45424,RMVar_hsa_circ_251404,RMVar_hsa_circ_251405,RMVar_hsa_circ_265821,RMVar_hsa_circ_67504,RMVar_hsa_circ_11369,RMVar_hsa_circ_360614,RMVar_hsa_circ_353349 51880 RMVar_ID_51880 Human_SNP_ID_359771124 A-to-I Human chr8 - 38301190 38301190 38301190 GAGGTGGGAGGATTGCTTGAGCCCAGGAATTCAAGACCAGCCTGGGCAACATAGCAAGACCTCGT GAGGTGGGAGGATTGCTTGAGCCCAGGAATTCCAGACCAGCCTGGGCAACATAGCAAGACCTCGT T G NSD3 Ensembl:ENSG00000147548 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1317789741 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_267769,RMVar_hsa_circ_37839,RMVar_hsa_circ_7392,RMVar_hsa_circ_18206,RMVar_hsa_circ_268860,RMVar_hsa_circ_118503,RMVar_hsa_circ_323712,RMVar_hsa_circ_45424,RMVar_hsa_circ_251404,RMVar_hsa_circ_251405,RMVar_hsa_circ_265821,RMVar_hsa_circ_67504,RMVar_hsa_circ_11369,RMVar_hsa_circ_360614,RMVar_hsa_circ_353349 51881 RMVar_ID_51881 Human_SNP_ID_359771137 A-to-I Human chr8 - 38301265 38301265 38301265 CCCATATAACTTTTATTAGAAGACTCTGGCTGAGCACCATGGCTCATGCCTGTAATTCCAGCATT CCCATATAACTTTTATTAGAAGACTCTGGCTGGGCACCATGGCTCATGCCTGTAATTCCAGCATT T C NSD3 Ensembl:ENSG00000147548 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1018896888 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16411556,Human_RBP_ID_17578786 RMVar_hsa_circ_267769,RMVar_hsa_circ_37839,RMVar_hsa_circ_7392,RMVar_hsa_circ_18206,RMVar_hsa_circ_268860,RMVar_hsa_circ_118503,RMVar_hsa_circ_323712,RMVar_hsa_circ_45424,RMVar_hsa_circ_251404,RMVar_hsa_circ_251405,RMVar_hsa_circ_265821,RMVar_hsa_circ_67504,RMVar_hsa_circ_11369,RMVar_hsa_circ_360614,RMVar_hsa_circ_353349 51882 RMVar_ID_51882 Human_SNP_ID_359774869 A-to-I Human chr8 - 38318946 38318946 38318946 AAATTCTTTGTTAATGCTGTATTTTTCTGTCCAAACAGGTTGAAACAGTTCCTCAGGCTACAGTG AAATTCTTTGTTAATGCTGTATTTTTCTGTCCGAACAGGTTGAAACAGTTCCTCAGGCTACAGTG T C NSD3 Ensembl:ENSG00000147548 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs757003869 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_957694,Human_RBP_ID_5405293,Human_RBP_ID_9351538 Human_Splice_Rec_966551,Human_Splice_Rec_966595,Human_Splice_Rec_966643,Human_Splice_Rec_966691,Human_Splice_Rec_966693 RMVar_hsa_circ_11761,RMVar_hsa_circ_37839,RMVar_hsa_circ_7392,RMVar_hsa_circ_268860,RMVar_hsa_circ_265821,RMVar_hsa_circ_105123,RMVar_hsa_circ_11369,RMVar_hsa_circ_251411,RMVar_hsa_circ_307923,RMVar_hsa_circ_77767,RMVar_hsa_circ_61635,RMVar_hsa_circ_266638,RMVar_hsa_circ_251412,RMVar_hsa_circ_266539,RMVar_hsa_circ_86315,RMVar_hsa_circ_251413,RMVar_hsa_circ_251414,RMVar_hsa_circ_35788 51883 RMVar_ID_51883 Human_SNP_ID_359775784 A-to-I Human chr8 - 38323733 38323733 38323733 ACCTTAAACTCCTGGACTCCAGAGATCCTCCTACCTCAGCCTCCTGGAGTAGCTGAGACTACCCA ACCTTAAACTCCTGGACTCCAGAGATCCTCCTGCCTCAGCCTCCTGGAGTAGCTGAGACTACCCA T C NSD3 Ensembl:ENSG00000147548 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs368119321 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_11761,RMVar_hsa_circ_37839,RMVar_hsa_circ_7392,RMVar_hsa_circ_268860,RMVar_hsa_circ_265821,RMVar_hsa_circ_105123,RMVar_hsa_circ_11369,RMVar_hsa_circ_251411,RMVar_hsa_circ_307923,RMVar_hsa_circ_56603,RMVar_hsa_circ_77767,RMVar_hsa_circ_61635,RMVar_hsa_circ_266638,RMVar_hsa_circ_251412,RMVar_hsa_circ_86315,RMVar_hsa_circ_251413,RMVar_hsa_circ_251414,RMVar_hsa_circ_35788,RMVar_hsa_circ_299235,RMVar_hsa_circ_251415 51884 RMVar_ID_51884 Human_SNP_ID_359779556 A-to-I Human chr8 - 38340462 38340462 38340462 GTGGTGGTGCGGGCCTGTATTCCCAGTTTCTCAGGAGGCTAAAGGAGGAGAACCACTTGAACCTG GTGGTGGTGCGGGCCTGTATTCCCAGTTTCTCGGGAGGCTAAAGGAGGAGAACCACTTGAACCTG T C NSD3 Ensembl:ENSG00000147548 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1301365286 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37839,RMVar_hsa_circ_105123,RMVar_hsa_circ_251411,RMVar_hsa_circ_307923,RMVar_hsa_circ_56603,RMVar_hsa_circ_77767,RMVar_hsa_circ_61635,RMVar_hsa_circ_251412,RMVar_hsa_circ_251413,RMVar_hsa_circ_35788,RMVar_hsa_circ_63330,RMVar_hsa_circ_326229,RMVar_hsa_circ_347219,RMVar_hsa_circ_251418,RMVar_hsa_circ_305753 51885 RMVar_ID_51885 Human_SNP_ID_359780170 A-to-I Human chr8 - 38343026 38343026 38343026 ACACTCAGCTAATTTTTTTGTGTATTTTTAGTAGAGACGGGGTTTCGCCATGTTGGCCAGGCTGA ACACTCAGCTAATTTTTTTGTGTATTTTTAGTGGAGACGGGGTTTCGCCATGTTGGCCAGGCTGA T C NSD3 Ensembl:ENSG00000147548 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs543929353 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37839,RMVar_hsa_circ_105123,RMVar_hsa_circ_251411,RMVar_hsa_circ_307923,RMVar_hsa_circ_56603,RMVar_hsa_circ_77767,RMVar_hsa_circ_61635,RMVar_hsa_circ_251412,RMVar_hsa_circ_251413,RMVar_hsa_circ_35788,RMVar_hsa_circ_63330,RMVar_hsa_circ_326229,RMVar_hsa_circ_347219,RMVar_hsa_circ_251418,RMVar_hsa_circ_305753 51886 RMVar_ID_51886 Human_SNP_ID_359780274 A-to-I Human chr8 - 38343540 38343540 38343540 TGCCACCACGCCTGGCTAGTTTTTGTATTTTTAGTAGAGATGGGGTTTCATTATGTTGGCCAGGC TGCCACCACGCCTGGCTAGTTTTTGTATTTTTGGTAGAGATGGGGTTTCATTATGTTGGCCAGGC T C NSD3 Ensembl:ENSG00000147548 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1311773758 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_37839,RMVar_hsa_circ_105123,RMVar_hsa_circ_251411,RMVar_hsa_circ_307923,RMVar_hsa_circ_56603,RMVar_hsa_circ_77767,RMVar_hsa_circ_61635,RMVar_hsa_circ_251412,RMVar_hsa_circ_251413,RMVar_hsa_circ_35788,RMVar_hsa_circ_63330,RMVar_hsa_circ_326229,RMVar_hsa_circ_347219,RMVar_hsa_circ_251418,RMVar_hsa_circ_305753 51887 RMVar_ID_51887 Human_SNP_ID_359787024 A-to-I Human chr8 - 38372967 38372967 38372967 CGGCTCACTGCAACCTCCGCGTCCCGGGTTCAAGCGATTCGCCTGCGTCAGCCTTCCGAGTAGCT CGGCTCACTGCAACCTCCGCGTCCCGGGTTCACGCGATTCGCCTGCGTCAGCCTTCCGAGTAGCT T G NSD3 Ensembl:ENSG00000147548 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs113052451 Functional Loss SNV dbSNP153 33..33 33 - - - 51888 RMVar_ID_51888 Human_SNP_ID_359795419 A-to-I Human chr8 - 38406541 38406541 38406541 GGAGTGCAGTGGCTCGATCTCGGCTCACTGCAACCTCCACCTCATGGGTTCAAGCAATTCTCCCT GGAGTGCAGTGGCTCGATCTCGGCTCACTGCAGCCTCCACCTCATGGGTTCAAGCAATTCTCCCT T C FGFR1 Ensembl:ENSG00000077782 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1336832486 Functional Loss SNV dbSNP153 33..33 33 - - - 51889 RMVar_ID_51889 Human_SNP_ID_359806662 A-to-I Human chr8 - 38445760 38445760 38445760 GAGGCGGGCAGATCACCTGAAGTCAGGAGTTCAAGCCCAGCCTGGCCAACATAGTGTCTCTACTA GAGGCGGGCAGATCACCTGAAGTCAGGAGTTCGAGCCCAGCCTGGCCAACATAGTGTCTCTACTA T C FGFR1 Ensembl:ENSG00000077782 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1403057957 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77152,RMVar_hsa_circ_251423,RMVar_hsa_circ_99803,RMVar_hsa_circ_251430,RMVar_hsa_circ_347223,RMVar_hsa_circ_267850,RMVar_hsa_circ_251434,RMVar_hsa_circ_375786,RMVar_hsa_circ_251436,RMVar_hsa_circ_251438,RMVar_hsa_circ_372519 51890 RMVar_ID_51890 Human_SNP_ID_359806665 A-to-I Human chr8 - 38445783 38445783 38445783 TAATCCCAGCATTTTGGGAGGTTGAGGCGGGCAGATCACCTGAAGTCAGGAGTTCAAGCCCAGCC TAATCCCAGCATTTTGGGAGGTTGAGGCGGGCGGATCACCTGAAGTCAGGAGTTCAAGCCCAGCC T C FGFR1 Ensembl:ENSG00000077782 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1465412050 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77152,RMVar_hsa_circ_251423,RMVar_hsa_circ_99803,RMVar_hsa_circ_251430,RMVar_hsa_circ_347223,RMVar_hsa_circ_267850,RMVar_hsa_circ_251434,RMVar_hsa_circ_375786,RMVar_hsa_circ_251436,RMVar_hsa_circ_251438,RMVar_hsa_circ_372519 51891 RMVar_ID_51891 Human_SNP_ID_359810431 A-to-I Human chr8 - 38460169 38460169 38460169 CTTTTAGTTAGTTAGTTTTGAGACAGAGTCTCACTCCGTCACCCAGGCTGGAGTGCAGTGATGCA CTTTTAGTTAGTTAGTTTTGAGACAGAGTCTCGCTCCGTCACCCAGGCTGGAGTGCAGTGATGCA T C FGFR1 Ensembl:ENSG00000077782 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1301837930 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_77152,RMVar_hsa_circ_251423,RMVar_hsa_circ_267850,RMVar_hsa_circ_323736 51892 RMVar_ID_51892 Human_SNP_ID_359882335 A-to-I Human chr8 + 38746017 38746017 38746017 TTAAATATTTTTTGTAGACATGGGGTCTTGCTATGTTGCCTAGGCTGGTCTTAAACTCCTGGCTT TTAAATATTTTTTGTAGACATGGGGTCTTGCTGTGTTGCCTAGGCTGGTCTTAAACTCCTGGCTT A G TACC1 Ensembl:ENSG00000147526 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1481317875 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_251440,RMVar_hsa_circ_116595,RMVar_hsa_circ_61214 51893 RMVar_ID_51893 Human_SNP_ID_359891320 A-to-I Human chr8 + 38784411 38784410 38784411 AACATGATGAAACCCCGTCTCTACTAAAAAATAAAAAAATTAGCTGGGCATGGTGGCAGGAACCT AACATGATGAAACCCCGTCTCTACTAAAAAAT_AAAAAATTAGCTGGGCATGGTGGCAGGAACCT TA T TACC1 Ensembl:ENSG00000147526 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1162675143 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_251440,RMVar_hsa_circ_116595,RMVar_hsa_circ_61214 51894 RMVar_ID_51894 Human_SNP_ID_359903883 A-to-I Human chr8 + 38837458 38837458 38837458 AAAAATAAAAATAAAATAAAAGACAAGATCTCACTCTGTCACCCAGGCTGAGTGCAGTGGCACAA AAAAATAAAAATAAAATAAAAGACAAGATCTCTCTCTGTCACCCAGGCTGAGTGCAGTGGCACAA A T TACC1 Ensembl:ENSG00000147526 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1159703666 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_64559,RMVar_hsa_circ_267429,RMVar_hsa_circ_51017,RMVar_hsa_circ_66600,RMVar_hsa_circ_352370,RMVar_hsa_circ_363206,RMVar_hsa_circ_251447,RMVar_hsa_circ_87993,RMVar_hsa_circ_251449,RMVar_hsa_circ_104768,RMVar_hsa_circ_281183,RMVar_hsa_circ_333530,RMVar_hsa_circ_251450,RMVar_hsa_circ_251448 51895 RMVar_ID_51895 Human_SNP_ID_359906872 A-to-I Human chr8 + 38850601 38850601 38850601 ATCACTTGAGTCCAGGAGTTTGAAACCTACCTAGGCAACATGGTGAAACCTTGTCTCTACCAAAA ATCACTTGAGTCCAGGAGTTTGAAACCTACCTGGGCAACATGGTGAAACCTTGTCTCTACCAAAA A G TACC1 Ensembl:ENSG00000147526 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1136120 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104768,RMVar_hsa_circ_251450 51896 RMVar_ID_51896 Human_SNP_ID_359921189 A-to-I Human chr8 + 38905824 38905824 38905824 TTCCTGCTTCAGCCTCCCAAGTAGCTGGGTCTACAGGCGCATGCCACCACGCCCAGCTAATTTTT TTCCTGCTTCAGCCTCCCAAGTAGCTGGGTCTGCAGGCGCATGCCACCACGCCCAGCTAATTTTT A G PLEKHA2 Ensembl:ENSG00000169499 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1428457023 Functional Loss SNV dbSNP153 33..33 33 - - - 51897 RMVar_ID_51897 Human_SNP_ID_359921591 A-to-I Human chr8 + 38907622 38907622 38907622 CAACCTACAAAAAATACAAAAATTAGCTGGGTATGGTGGTGCACGCCTGTAGTCCCAGCCACTCA CAACCTACAAAAAATACAAAAATTAGCTGGGTGTGGTGGTGCACGCCTGTAGTCCCAGCCACTCA A G PLEKHA2 Ensembl:ENSG00000169499 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1274682230 Functional Loss SNV dbSNP153 33..33 33 - - - 51898 RMVar_ID_51898 Human_SNP_ID_359921594 A-to-I Human chr8 + 38907640 38907640 38907640 AAAATTAGCTGGGTATGGTGGTGCACGCCTGTAGTCCCAGCCACTCAGGAGGCTGAGGTGGGAGG AAAATTAGCTGGGTATGGTGGTGCACGCCTGTTGTCCCAGCCACTCAGGAGGCTGAGGTGGGAGG A T PLEKHA2 Ensembl:ENSG00000169499 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1308645069 Functional Loss SNV dbSNP153 33..33 33 - - - 51899 RMVar_ID_51899 Human_SNP_ID_359922525 A-to-I Human chr8 + 38911766 38911766 38911766 GGAGGCTTGAGGCAGGAGGATTGCCTGGGTCTAAGAGTTTGAAAACAGCCTGGGCTATGTAGGGA GGAGGCTTGAGGCAGGAGGATTGCCTGGGTCTGAGAGTTTGAAAACAGCCTGGGCTATGTAGGGA A G PLEKHA2 Ensembl:ENSG00000169499 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs911427097 Functional Loss SNV dbSNP153 33..33 33 - - - 51900 RMVar_ID_51900 Human_SNP_ID_359930136 A-to-I Human chr8 + 38942318 38942318 38942318 CTAGCTACTCAGGAGGGTGAGGTGGAAGGATCACTTCAGTCTGAGAAGTCGAGGCTGCAGTGAGC CTAGCTACTCAGGAGGGTGAGGTGGAAGGATCCCTTCAGTCTGAGAAGTCGAGGCTGCAGTGAGC A C PLEKHA2 Ensembl:ENSG00000169499 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1232643946 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35066,RMVar_hsa_circ_340526,RMVar_hsa_circ_372201,RMVar_hsa_circ_251454,RMVar_hsa_circ_303768,RMVar_hsa_circ_349561,RMVar_hsa_circ_251452,RMVar_hsa_circ_373578,RMVar_hsa_circ_346147,RMVar_hsa_circ_251455,RMVar_hsa_circ_251453 51901 RMVar_ID_51901 Human_SNP_ID_359937545 A-to-I Human chr8 + 38971816 38971816 38971816 ATACGAAAAAAAAATTAGCCGGGCGCAGTGGCAGGCGCCTGTAGTCCCAGCTACTTGGGAGGCTG ATACGAAAAAAAAATTAGCCGGGCGCAGTGGCGGGCGCCTGTAGTCCCAGCTACTTGGGAGGCTG A G PLEKHA2 Ensembl:ENSG00000169499 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1158359684 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111676,RMVar_hsa_circ_251468 51902 RMVar_ID_51902 Human_SNP_ID_359937648 A-to-I Human chr8 + 38972210 38972210 38972210 TTTTAATTTTTTTTTTTTAATTTTTAAAAGACAGGGTCTCACTCTCTTACCCAGGCTAGAGTGCA TTTTAATTTTTTTTTTTTAATTTTTAAAAGACGGGGTCTCACTCTCTTACCCAGGCTAGAGTGCA A G PLEKHA2 Ensembl:ENSG00000169499 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1329864253 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111676,RMVar_hsa_circ_251468 51903 RMVar_ID_51903 Human_SNP_ID_359937651 A-to-I Human chr8 + 38972218 38972218 38972218 TTTTTTTTTTAATTTTTAAAAGACAGGGTCTCACTCTCTTACCCAGGCTAGAGTGCAGTGGTGTG TTTTTTTTTTAATTTTTAAAAGACAGGGTCTCGCTCTCTTACCCAGGCTAGAGTGCAGTGGTGTG A G PLEKHA2 Ensembl:ENSG00000169499 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1303813018 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16412894,Human_RBP_ID_18118434 RMVar_hsa_circ_111676,RMVar_hsa_circ_251468 51904 RMVar_ID_51904 Human_SNP_ID_359937656 A-to-I Human chr8 + 38972256 38972256 38972256 TTACCCAGGCTAGAGTGCAGTGGTGTGATCATAGTTCATCATAACTTTGAATCTCTGGGCTTAAG TTACCCAGGCTAGAGTGCAGTGGTGTGATCATGGTTCATCATAACTTTGAATCTCTGGGCTTAAG A G PLEKHA2 Ensembl:ENSG00000169499 Protein coding 3'UTR GSE38233;GSE100210;GSE107867;GSE107867;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;ASD brains,frontal_cortex;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,30559470,30559470,32596459 RNA-Seq:(High) rs1373868720 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111676,RMVar_hsa_circ_251468 51905 RMVar_ID_51905 Human_SNP_ID_359937667 A-to-I Human chr8 + 38972326 38972326 38972326 CTCCCATGTTAGCTTCCCAAGTAGCTAGGACTACAGGGTTGTGCTACCACGCCTGGCTAATTTTT CTCCCATGTTAGCTTCCCAAGTAGCTAGGACTGCAGGGTTGTGCTACCACGCCTGGCTAATTTTT A G PLEKHA2 Ensembl:ENSG00000169499 Protein coding 3'UTR GSE100210;GSE99789 HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 29129909,29796672 RNA-Seq:(High) rs1459271387 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111676,RMVar_hsa_circ_251468 51906 RMVar_ID_51906 Human_SNP_ID_359937701 A-to-I Human chr8 + 38972445 38972445 38972445 TGGCCCAAGTGATCCTCCTGCCTTGGCCTCCTAAAGTGTTGGGATTACAGGTGTGAGCCACTGCA TGGCCCAAGTGATCCTCCTGCCTTGGCCTCCTGAAGTGTTGGGATTACAGGTGTGAGCCACTGCA A G PLEKHA2 Ensembl:ENSG00000169499 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs550500036 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17578630,Human_RBP_ID_26558573 RMVar_hsa_circ_111676,RMVar_hsa_circ_251468 51907 RMVar_ID_51907 Human_SNP_ID_359937815 A-to-I Human chr8 + 38973017 38973017 38973017 TGGAGTGCAGTGGCCTGATCATGGCTCACTGCAGCCTGGACCTCCTGGGCTCAAGTGATCTTCCT TGGAGTGCAGTGGCCTGATCATGGCTCACTGCGGCCTGGACCTCCTGGGCTCAAGTGATCTTCCT A G PLEKHA2 Ensembl:ENSG00000169499 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs11553513 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_111676,RMVar_hsa_circ_251468 51908 RMVar_ID_51908 Human_SNP_ID_359950747 A-to-I Human chr8 + 39021484 39021484 39021484 TTTTGTATTTTTAGTAGAGAGAAGGTTTCGCCATGTTGGCTAGGCTGGTCTCGAACTCCTGACCT TTTTGTATTTTTAGTAGAGAGAAGGTTTCGCCTTGTTGGCTAGGCTGGTCTCGAACTCCTGACCT A T ADAM9 Ensembl:ENSG00000168615 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs984202849 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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 51909 RMVar_ID_51909 Human_SNP_ID_359950767 A-to-I Human chr8 + 39021552 39021552 39021552 GTGATCTACCCGCCTGGGCCTCTCAAAATGCTAGAATTACAGGCATGAGGTACTGCACCCGGCCT GTGATCTACCCGCCTGGGCCTCTCAAAATGCTGGAATTACAGGCATGAGGTACTGCACCCGGCCT A G ADAM9 Ensembl:ENSG00000168615 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1326388254 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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 51910 RMVar_ID_51910 Human_SNP_ID_359950770 A-to-I Human chr8 + 39021564 39021564 39021564 CCTGGGCCTCTCAAAATGCTAGAATTACAGGCATGAGGTACTGCACCCGGCCTTACATTTCTATT CCTGGGCCTCTCAAAATGCTAGAATTACAGGCGTGAGGTACTGCACCCGGCCTTACATTTCTATT A G ADAM9 Ensembl:ENSG00000168615 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1054096698 Functional Loss SNV dbSNP153 33..33 33 - - - 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_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 51911 RMVar_ID_51911 Human_SNP_ID_359976057 A-to-I Human chr8 + 39122280 39122280 39122280 GAATGTTATGAATTGAATTGTGTCCCCCGCCAAATCCATATGTTGAAAACCAAACTCCCAGTATG GAATGTTATGAATTGAATTGTGTCCCCCGCCAGATCCATATGTTGAAAACCAAACTCCCAGTATG A G ADAM32 Ensembl:ENSG00000197140 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs879873005 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_251491,RMVar_hsa_circ_297124,RMVar_hsa_circ_355861,RMVar_hsa_circ_363722,RMVar_hsa_circ_298602,RMVar_hsa_circ_330952,RMVar_hsa_circ_297208,RMVar_hsa_circ_44609,RMVar_hsa_circ_284154,RMVar_hsa_circ_251493,RMVar_hsa_circ_251494,RMVar_hsa_circ_251492 51912 RMVar_ID_51912 Human_SNP_ID_359976060 A-to-I Human chr8 + 39122287 39122287 39122287 ATGAATTGAATTGTGTCCCCCGCCAAATCCATATGTTGAAAACCAAACTCCCAGTATGGAGATAG ATGAATTGAATTGTGTCCCCCGCCAAATCCATTTGTTGAAAACCAAACTCCCAGTATGGAGATAG A T ADAM32 Ensembl:ENSG00000197140 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1413174967 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_251491,RMVar_hsa_circ_297124,RMVar_hsa_circ_355861,RMVar_hsa_circ_363722,RMVar_hsa_circ_298602,RMVar_hsa_circ_330952,RMVar_hsa_circ_297208,RMVar_hsa_circ_44609,RMVar_hsa_circ_284154,RMVar_hsa_circ_251493,RMVar_hsa_circ_251494,RMVar_hsa_circ_251492 51913 RMVar_ID_51913 Human_SNP_ID_359977909 A-to-I Human chr8 + 39130040 39130040 39130040 GCAGTGGCACAGTCTTGGCTCACTGCAACCTCAGCCTCCCAGGTTCAAGTGATTCTCCTGCCTCA GCAGTGGCACAGTCTTGGCTCACTGCAACCTCTGCCTCCCAGGTTCAAGTGATTCTCCTGCCTCA A T ADAM32 Ensembl:ENSG00000197140 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1338861099 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_968494,Human_Splice_Rec_968495 RMVar_hsa_circ_251491,RMVar_hsa_circ_297124,RMVar_hsa_circ_355861,RMVar_hsa_circ_363722,RMVar_hsa_circ_298602,RMVar_hsa_circ_330952,RMVar_hsa_circ_297208,RMVar_hsa_circ_44609,RMVar_hsa_circ_284154,RMVar_hsa_circ_251493,RMVar_hsa_circ_251494,RMVar_hsa_circ_251492 51914 RMVar_ID_51914 Human_SNP_ID_360443806 A-to-I Human chr8 - 40958353 40958352 40958354 ACCTAAACTGTAAAACTACTAGAAGAAAACATAGGAGAAAGCTTCATGACATTGGTTTGAGCAAC ACCTAAACTGTAAAACTACTAGAAGAAAACA__GGAGAAAGCTTCATGACATTGGTTTGAGCAAC CTA C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1200093904 Functional Loss DEL dbSNP153 32..33 33 - - - 51915 RMVar_ID_51915 Human_SNP_ID_360443809 A-to-I Human chr8 - 40958357 40958357 40958357 TAAGACCTAAACTGTAAAACTACTAGAAGAAAACATAGGAGAAAGCTTCATGACATTGGTTTGAG TAAGACCTAAACTGTAAAACTACTAGAAGAAAGCATAGGAGAAAGCTTCATGACATTGGTTTGAG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1254288647 Functional Loss SNV dbSNP153 33..33 33 - - - 51916 RMVar_ID_51916 Human_SNP_ID_360593469 A-to-I Human chr8 + 41531972 41531972 41531972 CACCACCACGCCTGGCTACTTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATATTGGGTTTCG CACCACCACGCCTGGCTACTTTTTGTATTTTTCGTAGAGATGGGGTTTCACCATATTGGGTTTCG A C GINS4 Ensembl:ENSG00000147536 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1407842665 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35370 51917 RMVar_ID_51917 Human_SNP_ID_360593470 A-to-I Human chr8 + 41531972 41531972 41531972 CACCACCACGCCTGGCTACTTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATATTGGGTTTCG CACCACCACGCCTGGCTACTTTTTGTATTTTTTGTAGAGATGGGGTTTCACCATATTGGGTTTCG A T GINS4 Ensembl:ENSG00000147536 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1407842665 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35370 51918 RMVar_ID_51918 Human_SNP_ID_360593487 A-to-I Human chr8 + 41532057 41532057 41532057 TTGAACTCCTGACCTTGTGATCTGCCTGCCTTAGCCTCCCAAAGTGCTGGGATTACAGGCATGAG TTGAACTCCTGACCTTGTGATCTGCCTGCCTTTGCCTCCCAAAGTGCTGGGATTACAGGCATGAG A T GINS4 Ensembl:ENSG00000147536 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1236768164 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_35370 51919 RMVar_ID_51919 Human_SNP_ID_360595096 A-to-I Human chr8 + 41538798 41538798 41538798 GCGATCTCAGCTCACTGCAACCTTCGCCCCCCAGGTTGACGTGATTCTGTTGCCTCAGCCTTCCA GCGATCTCAGCTCACTGCAACCTTCGCCCCCCGGGTTGACGTGATTCTGTTGCCTCAGCCTTCCA A G GINS4 Ensembl:ENSG00000147536 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1203363252 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_24258240 RMVar_hsa_circ_35370 51920 RMVar_ID_51920 Human_SNP_ID_360596034 A-to-I Human chr8 + 41542128 41542128 41542128 ATAAACAGCCAGGCATGGTGACTCAAGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGG ATAAACAGCCAGGCATGGTGACTCAAGCCTGTTATCCCAGCACTTTGGGAGGCCGAGGCGGGCGG A T GINS4 Ensembl:ENSG00000147536 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 23474544,24183664,29129909,29129909,32596459 RNA-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 51921 RMVar_ID_51921 Human_SNP_ID_360596036 A-to-I Human chr8 + 41542134 41542134 41542134 AGCCAGGCATGGTGACTCAAGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGGATCATG AGCCAGGCATGGTGACTCAAGCCTGTAATCCCGGCACTTTGGGAGGCCGAGGCGGGCGGATCATG A G GINS4 Ensembl:ENSG00000147536 Protein coding 3'UTR GSE47997;GSE38233;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;cultured B-cells;Bronchiolar epithelium,BERP35T4 cell line - 23474544,24183664,31158229 RNA-Seq:(High) rs1411825517 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 51922 RMVar_ID_51922 Human_SNP_ID_360596038 A-to-I Human chr8 + 41542137 41542137 41542137 CAGGCATGGTGACTCAAGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGGATCATGAGG CAGGCATGGTGACTCAAGCCTGTAATCCCAGCCCTTTGGGAGGCCGAGGCGGGCGGATCATGAGG A C GINS4 Ensembl:ENSG00000147536 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1435901551 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 51923 RMVar_ID_51923 Human_SNP_ID_360596039 A-to-I Human chr8 + 41542137 41542137 41542137 CAGGCATGGTGACTCAAGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGGATCATGAGG CAGGCATGGTGACTCAAGCCTGTAATCCCAGCGCTTTGGGAGGCCGAGGCGGGCGGATCATGAGG A G GINS4 Ensembl:ENSG00000147536 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1435901551 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 51924 RMVar_ID_51924 Human_SNP_ID_360596066 A-to-I Human chr8 + 41542225 41542225 41542225 CAACATGGTGAAACCCCATCTTTACTAAAAATACAAAATAATTAGCCGGGTGTTGGTGGTGTGCA CAACATGGTGAAACCCCATCTTTACTAAAAATGCAAAATAATTAGCCGGGTGTTGGTGGTGTGCA A G GINS4 Ensembl:ENSG00000147536 Protein coding 3'UTR GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1430405550 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86479,RMVar_hsa_circ_251525 51925 RMVar_ID_51925 Human_SNP_ID_360596067 A-to-I Human chr8 + 41542227 41542227 41542227 ACATGGTGAAACCCCATCTTTACTAAAAATACAAAATAATTAGCCGGGTGTTGGTGGTGTGCACC ACATGGTGAAACCCCATCTTTACTAAAAATACGAAATAATTAGCCGGGTGTTGGTGGTGTGCACC A G GINS4 Ensembl:ENSG00000147536 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1479327446 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86479,RMVar_hsa_circ_251525 51926 RMVar_ID_51926 Human_SNP_ID_360596068 A-to-I Human chr8 + 41542236 41542236 41542236 AACCCCATCTTTACTAAAAATACAAAATAATTAGCCGGGTGTTGGTGGTGTGCACCTGTAATCCC AACCCCATCTTTACTAAAAATACAAAATAATTGGCCGGGTGTTGGTGGTGTGCACCTGTAATCCC A G GINS4 Ensembl:ENSG00000147536 Protein coding 3'UTR GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs1171343884 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86479,RMVar_hsa_circ_251525 51927 RMVar_ID_51927 Human_SNP_ID_360596156 A-to-I Human chr8 + 41542502 41542501 41542502 ATCTCTACTAAACCCATCTCTACTAAAAATACAAAAAATTAGCCAGGCATGGTGGCGGGCCCATC ATCTCTACTAAACCCATCTCTACTAAAAATAC_AAAAATTAGCCAGGCATGGTGGCGGGCCCATC CA C GINS4 Ensembl:ENSG00000147536 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1351604453 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_21954974 RMVar_hsa_circ_86479,RMVar_hsa_circ_251525 51928 RMVar_ID_51928 Human_SNP_ID_360596165 A-to-I Human chr8 + 41542540 41542540 41542540 TTAGCCAGGCATGGTGGCGGGCCCATCTACTCAGGAGGCTGAGGCAGGAGAATGGTGTGAACCCG TTAGCCAGGCATGGTGGCGGGCCCATCTACTCGGGAGGCTGAGGCAGGAGAATGGTGTGAACCCG A G GINS4 Ensembl:ENSG00000147536 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line - 24183664,29129909,31158229,31158229,31158229,32596459,32596459 RNA-Seq:(High) rs944099583 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16414534,Human_RBP_ID_21954974 RMVar_hsa_circ_86479,RMVar_hsa_circ_251525 51929 RMVar_ID_51929 Human_SNP_ID_360596517 A-to-I Human chr8 + 41543805 41543804 41543806 ACGGCTCACTGCAGCCTCCACCTCCTGGGTTCAAGAGATTCTCCTGCCCCAGCCTCCCGAGTAGC ACGGCTCACTGCAGCCTCCACCTCCTGGGTTC__GAGATTCTCCTGCCCCAGCCTCCCGAGTAGC CAA C GINS4 Ensembl:ENSG00000147536 Protein coding 3'UTR GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,29796672,31158229,31158229,31158229,31158229 RNA-Seq:(High) rs1333365616 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_86479,RMVar_hsa_circ_251525 51930 RMVar_ID_51930 Human_SNP_ID_360596524 A-to-I Human chr8 + 41543832 41543832 41543832 GGTTCAAGAGATTCTCCTGCCCCAGCCTCCCGAGTAGCTGGTATTATAGGTGCACACCACCACAC GGTTCAAGAGATTCTCCTGCCCCAGCCTCCCGGGTAGCTGGTATTATAGGTGCACACCACCACAC A G GINS4 Ensembl:ENSG00000147536 Protein coding 3'UTR GSE47997;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 23474544,29129909,29796672,31158229,31158229,31158229 RNA-Seq:(High) rs952399704 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86479,RMVar_hsa_circ_251525 51931 RMVar_ID_51931 Human_SNP_ID_360596532 A-to-I Human chr8 + 41543871 41543871 41543871 GGTATTATAGGTGCACACCACCACACCCAACTAATTTTTTGTATTTTTAGTAGAGATGGGGTTTC GGTATTATAGGTGCACACCACCACACCCAACTGATTTTTTGTATTTTTAGTAGAGATGGGGTTTC A G GINS4 Ensembl:ENSG00000147536 Protein coding 3'UTR GSE47997;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T1 cell line - 23474544,31158229,31158229,31158229 RNA-Seq:(High) rs1480027729 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_179232 RMVar_hsa_circ_86479,RMVar_hsa_circ_251525 51932 RMVar_ID_51932 Human_SNP_ID_360596550 A-to-I Human chr8 + 41543950 41543950 41543950 GCTGGTCTCGAGCTCCTGACCCCAGGTGATCCACCCACCTCGGCCTCCCAAAGTGCTGGAATTAT GCTGGTCTCGAGCTCCTGACCCCAGGTGATCCGCCCACCTCGGCCTCCCAAAGTGCTGGAATTAT A G GINS4 Ensembl:ENSG00000147536 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line - 24183664,29129909,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs1269545343 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86479,RMVar_hsa_circ_251525 51933 RMVar_ID_51933 Human_SNP_ID_360596555 A-to-I Human chr8 + 41543968 41543968 41543968 ACCCCAGGTGATCCACCCACCTCGGCCTCCCAAAGTGCTGGAATTATAGGCGTGAGCCACTGCGC ACCCCAGGTGATCCACCCACCTCGGCCTCCCAGAGTGCTGGAATTATAGGCGTGAGCCACTGCGC A G GINS4 Ensembl:ENSG00000147536 Protein coding 3'UTR GSE47997;GSE38233;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831 K562 cells&HepG2 cells;cultured B-cells;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line - 23474544,24183664,29796672,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs1424195388 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_86479,RMVar_hsa_circ_251525 51934 RMVar_ID_51934 Human_SNP_ID_360596557 A-to-I Human chr8 + 41543977 41543976 41543977 GATCCACCCACCTCGGCCTCCCAAAGTGCTGGAATTATAGGCGTGAGCCACTGCGCACGGCCTGG GATCCACCCACCTCGGCCTCCCAAAGTGCTGG_ATTATAGGCGTGAGCCACTGCGCACGGCCTGG GA G GINS4 Ensembl:ENSG00000147536 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1188084666 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_86479,RMVar_hsa_circ_251525 51935 RMVar_ID_51935 Human_SNP_ID_360596672 A-to-I Human chr8 - 41544464 41544464 41544464 CAGGCGATGGGTATGCACATTAAGGCTTAGGAAGCACACTGTTCTAGGTTAACAGCTCAGGTCTC CAGGCGATGGGTATGCACATTAAGGCTTAGGAGGCACACTGTTCTAGGTTAACAGCTCAGGTCTC T C AC009630.2,AC009630.1 Ensembl:ENSG00000253174,Ensembl:ENSG00000253133 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs573654784 Functional Loss SNV dbSNP153 33..33 33 - - - 51936 RMVar_ID_51936 Human_SNP_ID_360604214 A-to-I Human chr8 - 41573943 41573943 41573943 CCTCAAGTTATCCACCCACTTCAGCCTCCCAAAGTGCCGGAATTACAGGCATGAGCCACTGCGCC CCTCAAGTTATCCACCCACTTCAGCCTCCCAAGGTGCCGGAATTACAGGCATGAGCCACTGCGCC T C AC009630.1 Ensembl:ENSG00000253133 lincRNA intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1478733793 Functional Loss SNV dbSNP153 33..33 33 - - - 51937 RMVar_ID_51937 Human_SNP_ID_360615472 A-to-I Human chr8 + 41616336 41616336 41616336 CTTTTTCTTTTGAGGCAGGGTCTCAGTCTGTCACCCAGGCTGGAGTGCAGTGGCACAATCATGAC CTTTTTCTTTTGAGGCAGGGTCTCAGTCTGTCGCCCAGGCTGGAGTGCAGTGGCACAATCATGAC A G GPAT4 Ensembl:ENSG00000158669 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1472142675 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83473,RMVar_hsa_circ_100650,RMVar_hsa_circ_251528,RMVar_hsa_circ_251535,RMVar_hsa_circ_109258,RMVar_hsa_circ_103656,RMVar_hsa_circ_359714,RMVar_hsa_circ_251537,RMVar_hsa_circ_251538 51938 RMVar_ID_51938 Human_SNP_ID_360615503 A-to-I Human chr8 + 41616478 41616478 41616478 CCACCACACCTGGCTAATTTTTTAATTTTTGTAGAGACGGAGTTTCCCCGCGTTGCTCAGACTGA CCACCACACCTGGCTAATTTTTTAATTTTTGTGGAGACGGAGTTTCCCCGCGTTGCTCAGACTGA A G GPAT4 Ensembl:ENSG00000158669 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1240047897 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7836503,Human_RBP_ID_16415255 RMVar_hsa_circ_83473,RMVar_hsa_circ_100650,RMVar_hsa_circ_251528,RMVar_hsa_circ_251535,RMVar_hsa_circ_109258,RMVar_hsa_circ_103656,RMVar_hsa_circ_359714,RMVar_hsa_circ_251537,RMVar_hsa_circ_251538 51939 RMVar_ID_51939 Human_SNP_ID_360615516 A-to-I Human chr8 + 41616506 41616506 41616506 TTGTAGAGACGGAGTTTCCCCGCGTTGCTCAGACTGATCTAGAACTCCTGGACTCAAGTGATCCG TTGTAGAGACGGAGTTTCCCCGCGTTGCTCAGGCTGATCTAGAACTCCTGGACTCAAGTGATCCG A G GPAT4 Ensembl:ENSG00000158669 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1056387974 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16415256 RMVar_hsa_circ_83473,RMVar_hsa_circ_100650,RMVar_hsa_circ_251528,RMVar_hsa_circ_251535,RMVar_hsa_circ_109258,RMVar_hsa_circ_103656,RMVar_hsa_circ_359714,RMVar_hsa_circ_251537,RMVar_hsa_circ_251538 51940 RMVar_ID_51940 Human_SNP_ID_360615521 A-to-I Human chr8 + 41616514 41616514 41616514 ACGGAGTTTCCCCGCGTTGCTCAGACTGATCTAGAACTCCTGGACTCAAGTGATCCGCCTGCCTT ACGGAGTTTCCCCGCGTTGCTCAGACTGATCTGGAACTCCTGGACTCAAGTGATCCGCCTGCCTT A G GPAT4 Ensembl:ENSG00000158669 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,cerebellum - 29129909,30559470 RNA-Seq:(High) rs1338393321 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16415256 RMVar_hsa_circ_83473,RMVar_hsa_circ_100650,RMVar_hsa_circ_251528,RMVar_hsa_circ_251535,RMVar_hsa_circ_109258,RMVar_hsa_circ_103656,RMVar_hsa_circ_359714,RMVar_hsa_circ_251537,RMVar_hsa_circ_251538 51941 RMVar_ID_51941 Human_SNP_ID_360705103 A-to-I Human chr8 - 41966296 41966296 41966296 GATAAAATTTGCACCGAGGCTGACGACAGGTAACTAGAACCTCGAAAAGCAAAGCTGGGGATAAG GATAAAATTTGCACCGAGGCTGACGACAGGTACCTAGAACCTCGAAAAGCAAAGCTGGGGATAAG T G KAT6A Ensembl:ENSG00000083168 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1380459205 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_264802,RMVar_hsa_circ_115175,RMVar_hsa_circ_251556,RMVar_hsa_circ_251557,RMVar_hsa_circ_341576 51942 RMVar_ID_51942 Human_SNP_ID_360705130 A-to-I Human chr8 - 41966403 41966403 41966403 TACTGAACCCTGTATGTACTGTATTGTGTTACATGAATGTAGTCTGTCTCTCTCTAAATCTCTTA TACTGAACCCTGTATGTACTGTATTGTGTTACGTGAATGTAGTCTGTCTCTCTCTAAATCTCTTA T C KAT6A Ensembl:ENSG00000083168 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1043847545 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1224552 RMVar_hsa_circ_264802,RMVar_hsa_circ_115175,RMVar_hsa_circ_251556,RMVar_hsa_circ_251557,RMVar_hsa_circ_341576 51943 RMVar_ID_51943 Human_SNP_ID_360784439 A-to-I Human chr8 + 42273155 42273155 42273155 AATTATTTTAAATGTCGGGTGCAGTGGCTTACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGC AATTATTTTAAATGTCGGGTGCAGTGGCTTACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGC A G IKBKB Ensembl:ENSG00000104365 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs552663238 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18135,RMVar_hsa_circ_111277,RMVar_hsa_circ_81888,RMVar_hsa_circ_251573,RMVar_hsa_circ_251574 51944 RMVar_ID_51944 Human_SNP_ID_360787227 A-to-I Human chr8 + 42284321 42284321 42284321 TACTGAGGTGATGTCCTGGCGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGAC TACTGAGGTGATGTCCTGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGAC A G IKBKB Ensembl:ENSG00000104365 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1424721841 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18135,RMVar_hsa_circ_111277,RMVar_hsa_circ_81888,RMVar_hsa_circ_251573,RMVar_hsa_circ_251574 51945 RMVar_ID_51945 Human_SNP_ID_360787229 A-to-I Human chr8 + 42284327 42284327 42284327 GGTGATGTCCTGGCGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGACGGGTGG GGTGATGTCCTGGCGCAGTGGCTCACACCTGTGATCCCAGCACTTTGGGAGGCCGAGACGGGTGG A G IKBKB Ensembl:ENSG00000104365 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1173152035 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18135,RMVar_hsa_circ_111277,RMVar_hsa_circ_81888,RMVar_hsa_circ_251573,RMVar_hsa_circ_251574 51946 RMVar_ID_51946 Human_SNP_ID_360789930 A-to-I Human chr8 + 42295299 42295299 42295299 CACCACCACACCTGGCTAATTGTTGTATTTTTAGTAGAGACAGGGTTTCATCATGTTGGCCAGGA CACCACCACACCTGGCTAATTGTTGTATTTTTGGTAGAGACAGGGTTTCATCATGTTGGCCAGGA A G IKBKB Ensembl:ENSG00000104365 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs909872198 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18135,RMVar_hsa_circ_81888,RMVar_hsa_circ_70606,RMVar_hsa_circ_251574,RMVar_hsa_circ_310960,RMVar_hsa_circ_54584,RMVar_hsa_circ_52460,RMVar_hsa_circ_8956,RMVar_hsa_circ_55994,RMVar_hsa_circ_84512,RMVar_hsa_circ_267064,RMVar_hsa_circ_251576,RMVar_hsa_circ_24355 51947 RMVar_ID_51947 Human_SNP_ID_360790005 A-to-I Human chr8 + 42295554 42295554 42295554 CAAGACCAGCCTGACCGAGATGCTGAAACCCCATCTCTACCAAAAACACAAAAATTAGCTGGGCA CAAGACCAGCCTGACCGAGATGCTGAAACCCCGTCTCTACCAAAAACACAAAAATTAGCTGGGCA A G IKBKB Ensembl:ENSG00000104365 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1423042432 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_18135,RMVar_hsa_circ_81888,RMVar_hsa_circ_70606,RMVar_hsa_circ_251574,RMVar_hsa_circ_310960,RMVar_hsa_circ_54584,RMVar_hsa_circ_52460,RMVar_hsa_circ_8956,RMVar_hsa_circ_55994,RMVar_hsa_circ_84512,RMVar_hsa_circ_267064,RMVar_hsa_circ_251576,RMVar_hsa_circ_24355 51948 RMVar_ID_51948 Human_SNP_ID_360803806 A-to-I Human chr8 + 42353248 42353248 42353248 CTCCTGCCTCAGCCTCCCAAGTATCTGGGACTACAGGCTCCCACCACCACACCCGGCTAATTTTT CTCCTGCCTCAGCCTCCCAAGTATCTGGGACTGCAGGCTCCCACCACCACACCCGGCTAATTTTT A G POLB Ensembl:ENSG00000070501 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1450367612 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_284396,RMVar_hsa_circ_331538,RMVar_hsa_circ_327374,RMVar_hsa_circ_25864,RMVar_hsa_circ_251583,RMVar_hsa_circ_251584,RMVar_hsa_circ_251588,RMVar_hsa_circ_10982,RMVar_hsa_circ_67842,RMVar_hsa_circ_311753,RMVar_hsa_circ_251589,RMVar_hsa_circ_251591,RMVar_hsa_circ_299677,RMVar_hsa_circ_337405,RMVar_hsa_circ_343851,RMVar_hsa_circ_251592,RMVar_hsa_circ_251590 51949 RMVar_ID_51949 Human_SNP_ID_360806328 A-to-I Human chr8 + 42363381 42363381 42363381 AAACTCCGTCTCTACTAAAAATACAAAAAATTAGCTGGGCGTGGTGGTGTGCGCCTGTAGTCCCA AAACTCCGTCTCTACTAAAAATACAAAAAATTGGCTGGGCGTGGTGGTGTGCGCCTGTAGTCCCA A G POLB Ensembl:ENSG00000070501 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1321463455 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_251592,RMVar_hsa_circ_251593,RMVar_hsa_circ_127321,RMVar_hsa_circ_251601,RMVar_hsa_circ_369515,RMVar_hsa_circ_251604,RMVar_hsa_circ_251605,RMVar_hsa_circ_251603,RMVar_hsa_circ_359659 51950 RMVar_ID_51950 Human_SNP_ID_360815847 A-to-I Human chr8 + 42400857 42400857 42400857 CCAGCTAATTTTTGTATTTTTAGTAGAGACGGAGTTTTACCACGTTGGGCAGGATGGTCTCTGTC CCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTTACCACGTTGGGCAGGATGGTCTCTGTC A G VDAC3 Ensembl:ENSG00000078668 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs920568004 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_79422,RMVar_hsa_circ_85173,RMVar_hsa_circ_251606,RMVar_hsa_circ_87158,RMVar_hsa_circ_354879,RMVar_hsa_circ_93033,RMVar_hsa_circ_251607,RMVar_hsa_circ_251608,RMVar_hsa_circ_251610,RMVar_hsa_circ_108824,RMVar_hsa_circ_251613,RMVar_hsa_circ_116007,RMVar_hsa_circ_251611,RMVar_hsa_circ_376475,RMVar_hsa_circ_270638,RMVar_hsa_circ_112547,RMVar_hsa_circ_251614,RMVar_hsa_circ_251612 51951 RMVar_ID_51951 Human_SNP_ID_360820177 A-to-I Human chr8 - 42418342 42418342 42418342 GCCAACATGGTGAAACCCCGTCTCTACTAAAAATATGAAAATTAGCCAAGGGTGATGGCATGCGC GCCAACATGGTGAAACCCCGTCTCTACTAAAACTATGAAAATTAGCCAAGGGTGATGGCATGCGC T G SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1238600866 Functional Loss SNV dbSNP153 33..33 33 - - - 51952 RMVar_ID_51952 Human_SNP_ID_360820178 A-to-I Human chr8 - 42418345 42418345 42418345 GTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATATGAAAATTAGCCAAGGGTGATGGCATG GTGGCCAACATGGTGAAACCCCGTCTCTACTACAAATATGAAAATTAGCCAAGGGTGATGGCATG T G SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1001644900 Functional Loss SNV dbSNP153 33..33 33 - - - 51953 RMVar_ID_51953 Human_SNP_ID_360820206 A-to-I Human chr8 - 42418511 42418511 42418511 GTGGTGGTGCTTGCCTGTAATCCCACCTACTCAGGAGGCTGAGACAGGAGAATCGCTTGAACCTG GTGGTGGTGCTTGCCTGTAATCCCACCTACTCGGGAGGCTGAGACAGGAGAATCGCTTGAACCTG T C SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1199517027 Functional Loss SNV dbSNP153 33..33 33 - - - 51954 RMVar_ID_51954 Human_SNP_ID_360821504 A-to-I Human chr8 - 42424456 42424456 42424456 CCTTAATTGGCCAGGTACGGTGGCTCATGCCTATAATCCTAGCTACTCGGGAGGCTGAGGCCGGA CCTTAATTGGCCAGGTACGGTGGCTCATGCCTGTAATCCTAGCTACTCGGGAGGCTGAGGCCGGA T C SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs959897190 Functional Loss SNV dbSNP153 33..33 33 - - - 51955 RMVar_ID_51955 Human_SNP_ID_360831933 A-to-I Human chr8 - 42464199 42464199 42464199 GGAGGCTGAGGTGGGAGGATCACTTGTACCTCAGAGGTTGAGGCTGCAGTGAGCCATGATTATGC GGAGGCTGAGGTGGGAGGATCACTTGTACCTCGGAGGTTGAGGCTGCAGTGAGCCATGATTATGC T C SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs565240275 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_371128,RMVar_hsa_circ_301763,RMVar_hsa_circ_104399,RMVar_hsa_circ_251618,RMVar_hsa_circ_251619,RMVar_hsa_circ_340718,RMVar_hsa_circ_251620,RMVar_hsa_circ_301501,RMVar_hsa_circ_251631,RMVar_hsa_circ_295481,RMVar_hsa_circ_251625,RMVar_hsa_circ_251626,RMVar_hsa_circ_251627,RMVar_hsa_circ_327110,RMVar_hsa_circ_337132,RMVar_hsa_circ_317040,RMVar_hsa_circ_271589,RMVar_hsa_circ_251628,RMVar_hsa_circ_251629,RMVar_hsa_circ_293837,RMVar_hsa_circ_251633,RMVar_hsa_circ_82848,RMVar_hsa_circ_251632,RMVar_hsa_circ_39391,RMVar_hsa_circ_350744 51956 RMVar_ID_51956 Human_SNP_ID_360831940 A-to-I Human chr8 - 42464232 42464232 42464232 GTGATGGTGCGCACTTGTAGTCCCAGCTACTCAGGAGGCTGAGGTGGGAGGATCACTTGTACCTC GTGATGGTGCGCACTTGTAGTCCCAGCTACTCGGGAGGCTGAGGTGGGAGGATCACTTGTACCTC T C SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1356129281 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_371128,RMVar_hsa_circ_301763,RMVar_hsa_circ_104399,RMVar_hsa_circ_251618,RMVar_hsa_circ_251619,RMVar_hsa_circ_340718,RMVar_hsa_circ_251620,RMVar_hsa_circ_301501,RMVar_hsa_circ_251631,RMVar_hsa_circ_295481,RMVar_hsa_circ_251625,RMVar_hsa_circ_251626,RMVar_hsa_circ_251627,RMVar_hsa_circ_327110,RMVar_hsa_circ_337132,RMVar_hsa_circ_317040,RMVar_hsa_circ_271589,RMVar_hsa_circ_251628,RMVar_hsa_circ_251629,RMVar_hsa_circ_293837,RMVar_hsa_circ_251633,RMVar_hsa_circ_82848,RMVar_hsa_circ_251632,RMVar_hsa_circ_39391,RMVar_hsa_circ_350744 51957 RMVar_ID_51957 Human_SNP_ID_360832104 A-to-I Human chr8 - 42464859 42464859 42464859 GCAGTTCTCCTGCCTCAGCCTCCCGAGTAGCTAGGATTACAGGCACATGCCACCACGCCCAGCTC GCAGTTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCACATGCCACCACGCCCAGCTC T C SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs907941157 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_371128,RMVar_hsa_circ_301763,RMVar_hsa_circ_104399,RMVar_hsa_circ_251618,RMVar_hsa_circ_251619,RMVar_hsa_circ_340718,RMVar_hsa_circ_251620,RMVar_hsa_circ_301501,RMVar_hsa_circ_251631,RMVar_hsa_circ_295481,RMVar_hsa_circ_251625,RMVar_hsa_circ_251626,RMVar_hsa_circ_251627,RMVar_hsa_circ_327110,RMVar_hsa_circ_337132,RMVar_hsa_circ_317040,RMVar_hsa_circ_271589,RMVar_hsa_circ_251628,RMVar_hsa_circ_251629,RMVar_hsa_circ_293837,RMVar_hsa_circ_251633,RMVar_hsa_circ_82848,RMVar_hsa_circ_251632,RMVar_hsa_circ_39391,RMVar_hsa_circ_350744 51958 RMVar_ID_51958 Human_SNP_ID_360832110 A-to-I Human chr8 - 42464875 42464875 42464875 CGCCTCCCGAGTTCAAGCAGTTCTCCTGCCTCAGCCTCCCGAGTAGCTAGGATTACAGGCACATG CGCCTCCCGAGTTCAAGCAGTTCTCCTGCCTCGGCCTCCCGAGTAGCTAGGATTACAGGCACATG T C SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs895099835 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_371128,RMVar_hsa_circ_301763,RMVar_hsa_circ_104399,RMVar_hsa_circ_251618,RMVar_hsa_circ_251619,RMVar_hsa_circ_340718,RMVar_hsa_circ_251620,RMVar_hsa_circ_301501,RMVar_hsa_circ_251631,RMVar_hsa_circ_295481,RMVar_hsa_circ_251625,RMVar_hsa_circ_251626,RMVar_hsa_circ_251627,RMVar_hsa_circ_327110,RMVar_hsa_circ_337132,RMVar_hsa_circ_317040,RMVar_hsa_circ_271589,RMVar_hsa_circ_251628,RMVar_hsa_circ_251629,RMVar_hsa_circ_293837,RMVar_hsa_circ_251633,RMVar_hsa_circ_82848,RMVar_hsa_circ_251632,RMVar_hsa_circ_39391,RMVar_hsa_circ_350744 51959 RMVar_ID_51959 Human_SNP_ID_360832171 A-to-I Human chr8 - 42465143 42465143 42465143 TGAGGCAGGAGAATCACTTCAACCTGGAAGGCAGAGTTTGCAGTGAGCCGGGATCGAGTCACTGC TGAGGCAGGAGAATCACTTCAACCTGGAAGGCGGAGTTTGCAGTGAGCCGGGATCGAGTCACTGC T C SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1462034165 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_371128,RMVar_hsa_circ_301763,RMVar_hsa_circ_104399,RMVar_hsa_circ_251618,RMVar_hsa_circ_251619,RMVar_hsa_circ_340718,RMVar_hsa_circ_251620,RMVar_hsa_circ_301501,RMVar_hsa_circ_251631,RMVar_hsa_circ_295481,RMVar_hsa_circ_251625,RMVar_hsa_circ_251626,RMVar_hsa_circ_251627,RMVar_hsa_circ_327110,RMVar_hsa_circ_337132,RMVar_hsa_circ_317040,RMVar_hsa_circ_271589,RMVar_hsa_circ_251628,RMVar_hsa_circ_251629,RMVar_hsa_circ_293837,RMVar_hsa_circ_251633,RMVar_hsa_circ_82848,RMVar_hsa_circ_251632,RMVar_hsa_circ_39391,RMVar_hsa_circ_350744 51960 RMVar_ID_51960 Human_SNP_ID_360832186 A-to-I Human chr8 - 42465202 42465202 42465202 AATACAAAAATTAACTGGGCATGATGGCAGGTACCTGTAATCCCAGCTACTAGGGAGGCTGAGGC AATACAAAAATTAACTGGGCATGATGGCAGGTGCCTGTAATCCCAGCTACTAGGGAGGCTGAGGC T C SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs574942119 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_371128,RMVar_hsa_circ_301763,RMVar_hsa_circ_104399,RMVar_hsa_circ_251618,RMVar_hsa_circ_251619,RMVar_hsa_circ_340718,RMVar_hsa_circ_251620,RMVar_hsa_circ_301501,RMVar_hsa_circ_251631,RMVar_hsa_circ_295481,RMVar_hsa_circ_251625,RMVar_hsa_circ_251626,RMVar_hsa_circ_251627,RMVar_hsa_circ_327110,RMVar_hsa_circ_337132,RMVar_hsa_circ_317040,RMVar_hsa_circ_271589,RMVar_hsa_circ_251628,RMVar_hsa_circ_251629,RMVar_hsa_circ_293837,RMVar_hsa_circ_251633,RMVar_hsa_circ_82848,RMVar_hsa_circ_251632,RMVar_hsa_circ_39391,RMVar_hsa_circ_350744 51961 RMVar_ID_51961 Human_SNP_ID_360835957 A-to-I Human chr8 - 42480752 42480752 42480752 GAGAGGCTGAGGTAGGAGGATTGCTTGAGCCCAGGAGCTTAAGGCTGCAGTGAGCCATGATCATG GAGAGGCTGAGGTAGGAGGATTGCTTGAGCCCGGGAGCTTAAGGCTGCAGTGAGCCATGATCATG T C SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1381846575 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_251633,RMVar_hsa_circ_82848 51962 RMVar_ID_51962 Human_SNP_ID_360839047 A-to-I Human chr8 - 42492816 42492811 42492816 AGTTAGCCGGGCACGTGGTGACAGGCGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA AGTTAGCCGGGCACGTGGTGACAGGCGCCTGT_____CAGCTACTTGGGAGGCTGAGGCAGGAGA GGGACT G SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1177868796 Functional Loss DEL dbSNP153 33..37 33 - - - RMVar_hsa_circ_251633,RMVar_hsa_circ_82848 51963 RMVar_ID_51963 Human_SNP_ID_360839302 A-to-I Human chr8 - 42493959 42493959 42493959 TTTTAAATGTTTTATAGAGACAGGGTCTCGCTATGTTACCCAGGCTGGTCTTGAACTCCTGAACT TTTTAAATGTTTTATAGAGACAGGGTCTCGCTGTGTTACCCAGGCTGGTCTTGAACTCCTGAACT T C SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs763632978 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_251633,RMVar_hsa_circ_82848 51964 RMVar_ID_51964 Human_SNP_ID_360846193 A-to-I Human chr8 - 42524594 42524594 42524594 TTTAGTAGAGACAGGGTTTCACCATGTTGGCAAGGCTGGTCTCGAACTCCTGACCTTGTGATCTG TTTAGTAGAGACAGGGTTTCACCATGTTGGCAGGGCTGGTCTCGAACTCCTGACCTTGTGATCTG T C SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1388176518 Functional Loss SNV dbSNP153 33..33 33 - - - 51965 RMVar_ID_51965 Human_SNP_ID_360846877 A-to-I Human chr8 - 42526921 42526921 42526921 TTTCTATTTTTTTGTAAAGGCGGGGTCCTGCTATGTTGCTCAGGCAGTTCTCAAACTCCTGGACT TTTCTATTTTTTTGTAAAGGCGGGGTCCTGCTGTGTTGCTCAGGCAGTTCTCAAACTCCTGGACT T C SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1446210233 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_255460,Human_RBP_ID_10396833,Human_RBP_ID_16420297 51966 RMVar_ID_51966 Human_SNP_ID_360847078 A-to-I Human chr8 - 42527561 42527561 42527561 TTTCTCCATGTTGGTCTTGAACTCCCAACCTCAGGTGATCCGCCCTCCTCAGCCCCCCAAAGTGC TTTCTCCATGTTGGTCTTGAACTCCCAACCTCCGGTGATCCGCCCTCCTCAGCCCCCCAAAGTGC T G SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1335663883 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9225314 51967 RMVar_ID_51967 Human_SNP_ID_360847453 A-to-I Human chr8 - 42528804 42528804 42528804 AAATTAGTCGGGCATGGTGGCGCATGCCTATAATCCTGGCTACTCGGGAGGCTGAGGCAGGAGAA AAATTAGTCGGGCATGGTGGCGCATGCCTATACTCCTGGCTACTCGGGAGGCTGAGGCAGGAGAA T G SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1030981867 Functional Loss SNV dbSNP153 33..33 33 - - - 51968 RMVar_ID_51968 Human_SNP_ID_360847463 A-to-I Human chr8 - 42528831 42528827 42528831 GAAACCCCGTTTCTACTAAAAATACAAAAATTAGTCGGGCATGGTGGCGCATGCCTATAATCCTG GAAACCCCGTTTCTACTAAAAATACAAAAATT____GGGCATGGTGGCGCATGCCTATAATCCTG CGACT C SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1397090262 Functional Loss DEL dbSNP153 33..36 33 - - - 51969 RMVar_ID_51969 Human_SNP_ID_360847465 A-to-I Human chr8 - 42528831 42528831 42528831 GAAACCCCGTTTCTACTAAAAATACAAAAATTAGTCGGGCATGGTGGCGCATGCCTATAATCCTG GAAACCCCGTTTCTACTAAAAATACAAAAATTGGTCGGGCATGGTGGCGCATGCCTATAATCCTG T C SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1306583823 Functional Loss SNV dbSNP153 33..33 33 - - - 51970 RMVar_ID_51970 Human_SNP_ID_360847587 A-to-I Human chr8 - 42529177 42529177 42529177 ATCACTTGAGCCTTGGAGTTCAAGAGCAGCCTAGTTAACATAGCAAGACTCCATCTCTTTGAAAA ATCACTTGAGCCTTGGAGTTCAAGAGCAGCCTGGTTAACATAGCAAGACTCCATCTCTTTGAAAA T C SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs999815060 Functional Loss SNV dbSNP153 33..33 33 - - - 51971 RMVar_ID_51971 Human_SNP_ID_360848208 A-to-I Human chr8 - 42531895 42531895 42531895 AGAATTTCTTGAACCCGGGAGGCCGAGGTTGCAGTGAGCTGAGATCGCGCCACTGCACTCCAGCC AGAATTTCTTGAACCCGGGAGGCCGAGGTTGCGGTGAGCTGAGATCGCGCCACTGCACTCCAGCC T C SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1028652660 Functional Loss SNV dbSNP153 33..33 33 - - - 51972 RMVar_ID_51972 Human_SNP_ID_360848266 A-to-I Human chr8 - 42532032 42532032 42532032 ACAAGGTCAGGAGATTGAAACCATCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATACA ACAAGGTCAGGAGATTGAAACCATCCTGGCCAGCATGGTGAAACCCCGTCTCTACTAAAAATACA T C SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1133913 Functional Loss SNV dbSNP153 33..33 33 - - - 51973 RMVar_ID_51973 Human_SNP_ID_360848268 A-to-I Human chr8 - 42532045 42532045 42532045 AGTTGGGTGGATCACAAGGTCAGGAGATTGAAACCATCCTGGCCAACATGGTGAAACCCCGTCTC AGTTGGGTGGATCACAAGGTCAGGAGATTGAAGCCATCCTGGCCAACATGGTGAAACCCCGTCTC T C SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs868131348 Functional Loss SNV dbSNP153 33..33 33 - - - 51974 RMVar_ID_51974 Human_SNP_ID_360848274 A-to-I Human chr8 - 42532100 42532100 42532100 GAGACTGGCCAGGCACAGTGGCTCACACCTGTAATACCAGCACTTTGGGAGGCTGAGTTGGGTGG GAGACTGGCCAGGCACAGTGGCTCACACCTGTGATACCAGCACTTTGGGAGGCTGAGTTGGGTGG T C SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1133912 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23316125,Human_RBP_ID_26171778 51975 RMVar_ID_51975 Human_SNP_ID_360848281 A-to-I Human chr8 - 42532122 42532122 42532122 TCAGTAGTTAACAAAGCAGACAGAGACTGGCCAGGCACAGTGGCTCACACCTGTAATACCAGCAC TCAGTAGTTAACAAAGCAGACAGAGACTGGCCGGGCACAGTGGCTCACACCTGTAATACCAGCAC T C SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1041979179 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16420418 51976 RMVar_ID_51976 Human_SNP_ID_360848650 A-to-I Human chr8 - 42533433 42533433 42533433 TTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGGCCT TTTTGTATTTTTAGTAGAGACGGGGTTTCACCGTGTTGGCCAGGCTGGTCTTGAACTCCTGGCCT T C SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1305546170 Functional Loss SNV dbSNP153 33..33 33 - - - 51977 RMVar_ID_51977 Human_SNP_ID_360848656 A-to-I Human chr8 - 42533450 42533450 42533450 CACTAAGCCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGG CACTAAGCCCAGCTAATTTTTGTATTTTTAGTGGAGACGGGGTTTCACCATGTTGGCCAGGCTGG T C SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1165542522 Functional Loss SNV dbSNP153 33..33 33 - - - 51978 RMVar_ID_51978 Human_SNP_ID_360848663 A-to-I Human chr8 - 42533472 42533472 42533472 AGCTGGGATCACAGGCATGCGCCACTAAGCCCAGCTAATTTTTGTATTTTTAGTAGAGACGGGGT AGCTGGGATCACAGGCATGCGCCACTAAGCCCGGCTAATTTTTGTATTTTTAGTAGAGACGGGGT T C SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE38233;GSE107867 cultured B-cells;ASD brains,frontal_cortex - 24183664,30559470 RNA-Seq:(High) rs909071017 Functional Loss SNV dbSNP153 33..33 33 - - - 51979 RMVar_ID_51979 Human_SNP_ID_360848678 A-to-I Human chr8 - 42533516 42533516 42533516 CACCTCCTGGGCTCAAGCAGTTCTCGTGCTTCAGCCTCCCGAGTAGCTGGGATCACAGGCATGCG CACCTCCTGGGCTCAAGCAGTTCTCGTGCTTCTGCCTCCCGAGTAGCTGGGATCACAGGCATGCG T A SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1386486590 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23316127 51980 RMVar_ID_51980 Human_SNP_ID_360848679 A-to-I Human chr8 - 42533516 42533516 42533516 CACCTCCTGGGCTCAAGCAGTTCTCGTGCTTCAGCCTCCCGAGTAGCTGGGATCACAGGCATGCG CACCTCCTGGGCTCAAGCAGTTCTCGTGCTTCCGCCTCCCGAGTAGCTGGGATCACAGGCATGCG T G SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE107867 ASD brains,temporal_cortex - 30559470 RNA-Seq:(High) rs1386486590 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23316127 51981 RMVar_ID_51981 Human_SNP_ID_360848689 A-to-I Human chr8 - 42533530 42533530 42533530 TACTCTGTAACCTCCACCTCCTGGGCTCAAGCAGTTCTCGTGCTTCAGCCTCCCGAGTAGCTGGG TACTCTGTAACCTCCACCTCCTGGGCTCAAGCCGTTCTCGTGCTTCAGCCTCCCGAGTAGCTGGG T G SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE38233;GSE100210;GSE99789 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 24183664,29129909,29796672 RNA-Seq:(High) rs1460025894 Functional Loss SNV dbSNP153 33..33 33 - - - 51982 RMVar_ID_51982 Human_SNP_ID_360848691 A-to-I Human chr8 - 42533533 42533533 42533533 ACCTACTCTGTAACCTCCACCTCCTGGGCTCAAGCAGTTCTCGTGCTTCAGCCTCCCGAGTAGCT ACCTACTCTGTAACCTCCACCTCCTGGGCTCAGGCAGTTCTCGTGCTTCAGCCTCCCGAGTAGCT T C SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE100210;GSE99789 HepG2 cell line;esophageal squamous carcinoma cells,EC109 - 29129909,29796672 RNA-Seq:(High) rs1012395238 Functional Loss SNV dbSNP153 33..33 33 - - - 51983 RMVar_ID_51983 Human_SNP_ID_360848706 A-to-I Human chr8 - 42533581 42533581 42533581 TGTTGCCCAGGTTGGAGTGTGATGACGACGCAATCTCGGTAAATATAAACCTACTCTGTAACCTC TGTTGCCCAGGTTGGAGTGTGATGACGACGCATTCTCGGTAAATATAAACCTACTCTGTAACCTC T A SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs13252777 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9225322,Human_RBP_ID_21618541,Human_RBP_ID_23199546,Human_RBP_ID_23316128 51984 RMVar_ID_51984 Human_SNP_ID_360848707 A-to-I Human chr8 - 42533581 42533581 42533581 TGTTGCCCAGGTTGGAGTGTGATGACGACGCAATCTCGGTAAATATAAACCTACTCTGTAACCTC TGTTGCCCAGGTTGGAGTGTGATGACGACGCAGTCTCGGTAAATATAAACCTACTCTGTAACCTC T C SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs13252777 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_9225322,Human_RBP_ID_21618541,Human_RBP_ID_23199546,Human_RBP_ID_23316128 51985 RMVar_ID_51985 Human_SNP_ID_360848847 A-to-I Human chr8 - 42533784 42533784 42533784 CATGGTGGTGCACGCCTGTAATCCAGCTAGTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACCTG CATGGTGGTGCACGCCTGTAATCCAGCTAGTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCTG T C SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1048647039 Functional Loss SNV dbSNP153 33..33 33 - - - 51986 RMVar_ID_51986 Human_SNP_ID_360848852 A-to-I Human chr8 - 42533796 42533796 42533796 AAATTAGCCGGGCATGGTGGTGCACGCCTGTAATCCAGCTAGTCAGGAGGCTGAGGCAGGAGAAT AAATTAGCCGGGCATGGTGGTGCACGCCTGTAGTCCAGCTAGTCAGGAGGCTGAGGCAGGAGAAT T C SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1023798728 Functional Loss SNV dbSNP153 33..33 33 - - - 51987 RMVar_ID_51987 Human_SNP_ID_360848853 A-to-I Human chr8 - 42533797 42533797 42533797 AAAATTAGCCGGGCATGGTGGTGCACGCCTGTAATCCAGCTAGTCAGGAGGCTGAGGCAGGAGAA AAAATTAGCCGGGCATGGTGGTGCACGCCTGTGATCCAGCTAGTCAGGAGGCTGAGGCAGGAGAA T C SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1241760606 Functional Loss SNV dbSNP153 33..33 33 - - - 51988 RMVar_ID_51988 Human_SNP_ID_360848868 A-to-I Human chr8 - 42533826 42533825 42533826 GTGAAACCCCCGTCTCCACTAGAAATACAAAAATTAGCCGGGCATGGTGGTGCACGCCTGTAATC GTGAAACCCCCGTCTCCACTAGAAATACAAAA_TTAGCCGGGCATGGTGGTGCACGCCTGTAATC AT A SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1460606234 Functional Loss DEL dbSNP153 33..33 33 - - - 51989 RMVar_ID_51989 Human_SNP_ID_360848869 A-to-I Human chr8 - 42533832 42533832 42533832 AACATAGTGAAACCCCCGTCTCCACTAGAAATACAAAAATTAGCCGGGCATGGTGGTGCACGCCT AACATAGTGAAACCCCCGTCTCCACTAGAAATGCAAAAATTAGCCGGGCATGGTGGTGCACGCCT T C SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1009882117 Functional Loss SNV dbSNP153 33..33 33 - - - 51990 RMVar_ID_51990 Human_SNP_ID_360848872 A-to-I Human chr8 - 42533841 42533841 42533841 AGCCTGACCAACATAGTGAAACCCCCGTCTCCACTAGAAATACAAAAATTAGCCGGGCATGGTGG AGCCTGACCAACATAGTGAAACCCCCGTCTCCGCTAGAAATACAAAAATTAGCCGGGCATGGTGG T C SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs1021575450 Functional Loss SNV dbSNP153 33..33 33 - - - 51991 RMVar_ID_51991 Human_SNP_ID_360848879 A-to-I Human chr8 - 42533859 42533859 42533859 GGTCAGGAGTTCGAGACCAGCCTGACCAACATAGTGAAACCCCCGTCTCCACTAGAAATACAAAA GGTCAGGAGTTCGAGACCAGCCTGACCAACATGGTGAAACCCCCGTCTCCACTAGAAATACAAAA T C SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs78373392 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_10396881 51992 RMVar_ID_51992 Human_SNP_ID_360848890 A-to-I Human chr8 - 42533900 42533900 42533900 CGGGCATGGTGGCGTGAGAGGCCGAGGTGGGCAGATCACGAGGTCAGGAGTTCGAGACCAGCCTG CGGGCATGGTGGCGTGAGAGGCCGAGGTGGGCGGATCACGAGGTCAGGAGTTCGAGACCAGCCTG T C SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs910170262 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18118900 51993 RMVar_ID_51993 Human_SNP_ID_360848967 A-to-I Human chr8 - 42534132 42534132 42534132 TGGGATTTTTAGTAGAGAACAGGTTTCACCATATTGGCCAGGCTGGTCTTGAACTCGCAACCTCA TGGGATTTTTAGTAGAGAACAGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCGCAACCTCA T C SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE47997;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831 K562 cells&HepG2 cells;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line - 23474544,29796672,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs1450873818 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16420477,Human_RBP_ID_26171794 51994 RMVar_ID_51994 Human_SNP_ID_360848968 A-to-I Human chr8 - 42534134 42534134 42534134 GCTGGGATTTTTAGTAGAGAACAGGTTTCACCATATTGGCCAGGCTGGTCTTGAACTCGCAACCT GCTGGGATTTTTAGTAGAGAACAGGTTTCACCGTATTGGCCAGGCTGGTCTTGAACTCGCAACCT T C SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs942299837 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16420477 51995 RMVar_ID_51995 Human_SNP_ID_360848969 A-to-I Human chr8 - 42534137 42534137 42534137 GTAGCTGGGATTTTTAGTAGAGAACAGGTTTCACCATATTGGCCAGGCTGGTCTTGAACTCGCAA GTAGCTGGGATTTTTAGTAGAGAACAGGTTTCGCCATATTGGCCAGGCTGGTCTTGAACTCGCAA T C SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1335808960 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16420477 51996 RMVar_ID_51996 Human_SNP_ID_360848973 A-to-I Human chr8 - 42534154 42534154 42534154 GTGCCTTGGGCTCCCGAGTAGCTGGGATTTTTAGTAGAGAACAGGTTTCACCATATTGGCCAGGC GTGCCTTGGGCTCCCGAGTAGCTGGGATTTTTGGTAGAGAACAGGTTTCACCATATTGGCCAGGC T C SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs1451305357 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16420477 51997 RMVar_ID_51997 Human_SNP_ID_360848981 A-to-I Human chr8 - 42534193 42534193 42534193 CTAACTGCAACCGCTGCCTCCCAGGTACAAGTAATTCTCGTGCCTTGGGCTCCCGAGTAGCTGGG CTAACTGCAACCGCTGCCTCCCAGGTACAAGTGATTCTCGTGCCTTGGGCTCCCGAGTAGCTGGG T C SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs17357472 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7837919 51998 RMVar_ID_51998 Human_SNP_ID_360848982 A-to-I Human chr8 - 42534197 42534197 42534197 GCGGCTAACTGCAACCGCTGCCTCCCAGGTACAAGTAATTCTCGTGCCTTGGGCTCCCGAGTAGC GCGGCTAACTGCAACCGCTGCCTCCCAGGTACGAGTAATTCTCGTGCCTTGGGCTCCCGAGTAGC T C SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line - 23474544,29129909 RNA-Seq:(High) rs1437459074 Functional Loss SNV dbSNP153 33..33 33 - - - 51999 RMVar_ID_51999 Human_SNP_ID_360848984 A-to-I Human chr8 - 42534203 42534203 42534203 GCGATCGCGGCTAACTGCAACCGCTGCCTCCCAGGTACAAGTAATTCTCGTGCCTTGGGCTCCCG GCGATCGCGGCTAACTGCAACCGCTGCCTCCCGGGTACAAGTAATTCTCGTGCCTTGGGCTCCCG T C SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs17357465 Functional Loss SNV dbSNP153 33..33 33 - - - 52000 RMVar_ID_52000 Human_SNP_ID_360848992 A-to-I Human chr8 - 42534223 42534223 42534223 ACTGGTTGGAGTGCGATGATGCGATCGCGGCTAACTGCAACCGCTGCCTCCCAGGTACAAGTAAT ACTGGTTGGAGTGCGATGATGCGATCGCGGCTGACTGCAACCGCTGCCTCCCAGGTACAAGTAAT T C SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line - 29129909,31158229 RNA-Seq:(High) rs765649808 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7837920,Human_RBP_ID_16420480 52001 RMVar_ID_52001 Human_SNP_ID_360849013 A-to-I Human chr8 - 42534277 42534277 42534277 CTTCTTTCCTTTTTATTTATTTTTTTTGAGACAGAGTCTCATTCTGTCGCCCAGACTGGTTGGAG CTTCTTTCCTTTTTATTTATTTTTTTTGAGACGGAGTCTCATTCTGTCGCCCAGACTGGTTGGAG T C SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs3195740 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3159226,Human_RBP_ID_16512851 52002 RMVar_ID_52002 Human_SNP_ID_360849019 A-to-I Human chr8 - 42534295 42534295 42534295 TCGATGTCAGTGTTACCTCTTCTTTCCTTTTTATTTATTTTTTTTGAGACAGAGTCTCATTCTGT TCGATGTCAGTGTTACCTCTTCTTTCCTTTTTTTTTATTTTTTTTGAGACAGAGTCTCATTCTGT T A SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs9696 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7837921,Human_RBP_ID_16512851 52003 RMVar_ID_52003 Human_SNP_ID_360849020 A-to-I Human chr8 - 42534295 42534295 42534295 TCGATGTCAGTGTTACCTCTTCTTTCCTTTTTATTTATTTTTTTTGAGACAGAGTCTCATTCTGT TCGATGTCAGTGTTACCTCTTCTTTCCTTTTTGTTTATTTTTTTTGAGACAGAGTCTCATTCTGT T C SLC20A2 Ensembl:ENSG00000168575 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs9696 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7837921,Human_RBP_ID_16512851 52004 RMVar_ID_52004 Human_SNP_ID_360904052 A-to-I Human chr8 - 42752592 42752592 42752592 AAAAACAGTTTGGTCAGGTGTGGTGGCCTGTAATCCCAGCACTTTGGAGGCTGAGGAAGAAGGAT AAAAACAGTTTGGTCAGGTGTGGTGGCCTGTAGTCCCAGCACTTTGGAGGCTGAGGAAGAAGGAT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs201832457 Functional Loss SNV dbSNP153 33..33 33 - - - 52005 RMVar_ID_52005 Human_SNP_ID_360925205 A-to-I Human chr8 - 42834513 42834513 42834513 GGTGGTGCGCGCCTGTAGTCCCAGATGTGCTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACCTG GGTGGTGCGCGCCTGTAGTCCCAGATGTGCTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCTG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs982436982 Functional Loss SNV dbSNP153 33..33 33 - - - 52006 RMVar_ID_52006 Human_SNP_ID_360929670 A-to-I Human chr8 - 42851420 42851420 42851420 GCTGGGACTACAGATGCCCACCACCACACCCAACTAATTTTTCTATTTTTAGTAGAGACAGGGTT GCTGGGACTACAGATGCCCACCACCACACCCATCTAATTTTTCTATTTTTAGTAGAGACAGGGTT T A RNF170 Ensembl:ENSG00000120925 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1251562892 Functional Loss SNV dbSNP153 33..33 33 - - - 52007 RMVar_ID_52007 Human_SNP_ID_360931703 A-to-I Human chr8 - 42859443 42859434 42859443 TTTTATAGAGACTGGGTTTTGCCATGCTGCCCAGGCTGGCCTTGAACTCCTGGGCTCAAGCAATC TTTTATAGAGACTGGGTTTTGCCATGCTGCCC_________TTGAACTCCTGGGCTCAAGCAATC AGGCCAGCCT A RNF170 Ensembl:ENSG00000120925 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1411938232 Functional Loss DEL dbSNP153 33..41 33 - - - 52008 RMVar_ID_52008 Human_SNP_ID_360931725 A-to-I Human chr8 - 42859545 42859545 42859545 ACGGCTCACTGCAGCCTCAACCTTCCAAGCTCAGGCCATCCTGCCGCCTCAGCCTCCCAAGTAGC ACGGCTCACTGCAGCCTCAACCTTCCAAGCTCGGGCCATCCTGCCGCCTCAGCCTCCCAAGTAGC T C RNF170 Ensembl:ENSG00000120925 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1167426880 Functional Loss SNV dbSNP153 33..33 33 - - - 52009 RMVar_ID_52009 Human_SNP_ID_360931768 A-to-I Human chr8 - 42859724 42859724 42859724 GGACTGCTTGAGCCCGGGAGGCAGAGGTTGCAATGAGCCAGGATCACATCACTGCACTCCAGCCT GGACTGCTTGAGCCCGGGAGGCAGAGGTTGCAGTGAGCCAGGATCACATCACTGCACTCCAGCCT T C RNF170 Ensembl:ENSG00000120925 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1463662390 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17578636 52010 RMVar_ID_52010 Human_SNP_ID_360931769 A-to-I Human chr8 - 42859724 42859724 42859724 GGACTGCTTGAGCCCGGGAGGCAGAGGTTGCAATGAGCCAGGATCACATCACTGCACTCCAGCCT GGACTGCTTGAGCCCGGGAGGCAGAGGTTGCACTGAGCCAGGATCACATCACTGCACTCCAGCCT T G RNF170 Ensembl:ENSG00000120925 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1463662390 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17578636 52011 RMVar_ID_52011 Human_SNP_ID_360932224 A-to-I Human chr8 - 42861629 42861629 42861629 TTTGACTATGAGAAATCTTGGCCAGGCACAGTAGCTAACGCCTATAATCCTAGCACTTTGGGAGG TTTGACTATGAGAAATCTTGGCCAGGCACAGTGGCTAACGCCTATAATCCTAGCACTTTGGGAGG T C RNF170 Ensembl:ENSG00000120925 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1179987950 Functional Loss SNV dbSNP153 33..33 33 - - - 52012 RMVar_ID_52012 Human_SNP_ID_360940242 A-to-I Human chr8 - 42895297 42895297 42895297 TTTTTGTTGTTGTTGATGGTGGTTTTTGAGAAAGGGTCTCGTTCTGGAGTGCAGTGGCGCAATCT TTTTTGTTGTTGTTGATGGTGGTTTTTGAGAAGGGGTCTCGTTCTGGAGTGCAGTGGCGCAATCT T C RNF170 Ensembl:ENSG00000120925 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs930625169 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_83256,RMVar_hsa_circ_251652 52013 RMVar_ID_52013 Human_SNP_ID_360946072 A-to-I Human chr8 + 42915456 42915456 42915456 CCTGTTATTATTATTATTATTTTTAAAGACAGAGTCTTGCTCTTGTTGCCCAGGTCGGAGAGCAA CCTGTTATTATTATTATTATTTTTAAAGACAGTGTCTTGCTCTTGTTGCCCAGGTCGGAGAGCAA A T HOOK3 Ensembl:ENSG00000168172 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs755748329 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17578638 RMVar_hsa_circ_274233,RMVar_hsa_circ_98793,RMVar_hsa_circ_295337,RMVar_hsa_circ_315323,RMVar_hsa_circ_329461,RMVar_hsa_circ_337043,RMVar_hsa_circ_251658,RMVar_hsa_circ_370834,RMVar_hsa_circ_329509,RMVar_hsa_circ_316355,RMVar_hsa_circ_310122,RMVar_hsa_circ_315147,RMVar_hsa_circ_298247,RMVar_hsa_circ_286495,RMVar_hsa_circ_293387,RMVar_hsa_circ_285694,RMVar_hsa_circ_251664,RMVar_hsa_circ_251668,RMVar_hsa_circ_34033,RMVar_hsa_circ_104259,RMVar_hsa_circ_251669,RMVar_hsa_circ_251670,RMVar_hsa_circ_251666,RMVar_hsa_circ_251667,RMVar_hsa_circ_251665,RMVar_hsa_circ_251660,RMVar_hsa_circ_251662,RMVar_hsa_circ_251663,RMVar_hsa_circ_251661,RMVar_hsa_circ_251659 52014 RMVar_ID_52014 Human_SNP_ID_360953304 A-to-I Human chr8 + 42941397 42941397 42941397 AAAATTAGGTGGGTGTGGTGGTGGGCGCTTGTAGTCCCAGCTACTCGGGAGGCTGAGGCACGAGA AAAATTAGGTGGGTGTGGTGGTGGGCGCTTGTTGTCCCAGCTACTCGGGAGGCTGAGGCACGAGA A T HOOK3 Ensembl:ENSG00000168172 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1490714571 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_718,RMVar_hsa_circ_274233,RMVar_hsa_circ_98793,RMVar_hsa_circ_295337,RMVar_hsa_circ_315323,RMVar_hsa_circ_337043,RMVar_hsa_circ_251658,RMVar_hsa_circ_370834,RMVar_hsa_circ_329509,RMVar_hsa_circ_316355,RMVar_hsa_circ_310122,RMVar_hsa_circ_315147,RMVar_hsa_circ_298247,RMVar_hsa_circ_286495,RMVar_hsa_circ_293387,RMVar_hsa_circ_251664,RMVar_hsa_circ_251668,RMVar_hsa_circ_34033,RMVar_hsa_circ_104259,RMVar_hsa_circ_251669,RMVar_hsa_circ_251666,RMVar_hsa_circ_251667,RMVar_hsa_circ_251665,RMVar_hsa_circ_251660,RMVar_hsa_circ_251662,RMVar_hsa_circ_251663,RMVar_hsa_circ_251661,RMVar_hsa_circ_277634,RMVar_hsa_circ_331440,RMVar_hsa_circ_251659,RMVar_hsa_circ_336898,RMVar_hsa_circ_355554,RMVar_hsa_circ_332889,RMVar_hsa_circ_290952,RMVar_hsa_circ_280090,RMVar_hsa_circ_56313,RMVar_hsa_circ_273903,RMVar_hsa_circ_39640,RMVar_hsa_circ_9606,RMVar_hsa_circ_251674,RMVar_hsa_circ_251676,RMVar_hsa_circ_251677,RMVar_hsa_circ_251675,RMVar_hsa_circ_251672,RMVar_hsa_circ_251673,RMVar_hsa_circ_296052,RMVar_hsa_circ_327114,RMVar_hsa_circ_251679,RMVar_hsa_circ_314386,RMVar_hsa_circ_54874,RMVar_hsa_circ_251680,RMVar_hsa_circ_251681 52015 RMVar_ID_52015 Human_SNP_ID_360972712 A-to-I Human chr8 + 43020436 43020436 43020436 GGATCCAACTATTTTTAAAGCAAATTGGGGCCAGACGTGGTGCCTCACGCCTGCAATCTCACCAT GGATCCAACTATTTTTAAAGCAAATTGGGGCCGGACGTGGTGCCTCACGCCTGCAATCTCACCAT A G HOOK3,AC110275.1 Ensembl:ENSG00000168172,Ensembl:ENSG00000254673 Protein coding,Protein coding 3'UTR,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1252063821 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17578639 RMVar_hsa_circ_104259,RMVar_hsa_circ_251659,RMVar_hsa_circ_79637,RMVar_hsa_circ_251721 52016 RMVar_ID_52016 Human_SNP_ID_360972722 A-to-I Human chr8 + 43020458 43020458 43020458 AATTGGGGCCAGACGTGGTGCCTCACGCCTGCAATCTCACCATTTGGGAGACCTAGGTGGGGGTG AATTGGGGCCAGACGTGGTGCCTCACGCCTGCCATCTCACCATTTGGGAGACCTAGGTGGGGGTG A C HOOK3,AC110275.1 Ensembl:ENSG00000168172,Ensembl:ENSG00000254673 Protein coding,Protein coding 3'UTR,intron GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line - 24183664,29129909,29129909 RNA-Seq:(High) rs1331567091 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8687393,Human_RBP_ID_17578639 RMVar_hsa_circ_104259,RMVar_hsa_circ_251659,RMVar_hsa_circ_79637,RMVar_hsa_circ_251721 52017 RMVar_ID_52017 Human_SNP_ID_360972751 A-to-I Human chr8 + 43020575 43020575 43020575 CATCTCTACTAAATTACAAAAATTAGCTGGGCATGGTGGCATGTGGCTGTAATCCCAGCTACTTG CATCTCTACTAAATTACAAAAATTAGCTGGGCGTGGTGGCATGTGGCTGTAATCCCAGCTACTTG A G HOOK3,AC110275.1 Ensembl:ENSG00000168172,Ensembl:ENSG00000254673 Protein coding,Protein coding 3'UTR,intron GSE38233;GSE107867 cultured B-cells;ASD brains,frontal_cortex - 24183664,30559470 RNA-Seq:(High) rs1191269984 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104259,RMVar_hsa_circ_251659,RMVar_hsa_circ_79637,RMVar_hsa_circ_251721 52018 RMVar_ID_52018 Human_SNP_ID_360972761 A-to-I Human chr8 + 43020646 43020646 43020646 TGAGGCAGGAGAGTCACTTGAACTCAGGAGCCAGAGACTGCAGTGAGCTGAGATCGCACCACTGC TGAGGCAGGAGAGTCACTTGAACTCAGGAGCCGGAGACTGCAGTGAGCTGAGATCGCACCACTGC A G HOOK3,AC110275.1 Ensembl:ENSG00000168172,Ensembl:ENSG00000254673 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1563316417 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104259,RMVar_hsa_circ_251659,RMVar_hsa_circ_79637,RMVar_hsa_circ_251721 52019 RMVar_ID_52019 Human_SNP_ID_360972790 A-to-I Human chr8 + 43020829 43020829 43020829 GAATATGATGGATGAAAACAACAGCCAGGTGCAGTGGCTCACGCGTATAATCCCAGCACTTTGGG GAATATGATGGATGAAAACAACAGCCAGGTGCGGTGGCTCACGCGTATAATCCCAGCACTTTGGG A G HOOK3,AC110275.1 Ensembl:ENSG00000168172,Ensembl:ENSG00000254673 Protein coding,Protein coding 3'UTR,intron GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs139230267 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104259,RMVar_hsa_circ_251659,RMVar_hsa_circ_79637,RMVar_hsa_circ_251721 52020 RMVar_ID_52020 Human_SNP_ID_360972815 A-to-I Human chr8 + 43020947 43020944 43020948 ACATGGTGAAACTCCGTCTCTACTAAAAATACAAACAATTAGCCAGGCATGGTGGTGTGTGCCTG ACATGGTGAAACTCCGTCTCTACTAAAAAT____ACAATTAGCCAGGCATGGTGGTGTGTGCCTG TACAA T HOOK3,AC110275.1 Ensembl:ENSG00000168172,Ensembl:ENSG00000254673 Protein coding,Protein coding 3'UTR,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1390014580 Functional Loss DEL dbSNP153 31..34 33 - - - RMVar_hsa_circ_104259,RMVar_hsa_circ_251659,RMVar_hsa_circ_79637,RMVar_hsa_circ_251721 52021 RMVar_ID_52021 Human_SNP_ID_360972817 A-to-I Human chr8 + 43020963 43020963 43020963 TCTCTACTAAAAATACAAACAATTAGCCAGGCATGGTGGTGTGTGCCTGTAGTCCCAGCTACTTG TCTCTACTAAAAATACAAACAATTAGCCAGGCGTGGTGGTGTGTGCCTGTAGTCCCAGCTACTTG A G HOOK3,AC110275.1 Ensembl:ENSG00000168172,Ensembl:ENSG00000254673 Protein coding,Protein coding 3'UTR,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1180934668 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104259,RMVar_hsa_circ_251659,RMVar_hsa_circ_79637,RMVar_hsa_circ_251721 52022 RMVar_ID_52022 Human_SNP_ID_360972823 A-to-I Human chr8 + 43020991 43020991 43020991 AGGCATGGTGGTGTGTGCCTGTAGTCCCAGCTACTTGGGAGGGTGAGGCAGGAGAATTGCTTGAA AGGCATGGTGGTGTGTGCCTGTAGTCCCAGCTGCTTGGGAGGGTGAGGCAGGAGAATTGCTTGAA A G HOOK3,AC110275.1 Ensembl:ENSG00000168172,Ensembl:ENSG00000254673 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-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 52023 RMVar_ID_52023 Human_SNP_ID_360972980 A-to-I Human chr8 + 43021365 43021365 43021365 TCGTTCCGTCACCCAGGCTGTAGTGCCGTGGCATGATCTCGGCTCACTGCAGCCTCTGCCTCCCG TCGTTCCGTCACCCAGGCTGTAGTGCCGTGGCTTGATCTCGGCTCACTGCAGCCTCTGCCTCCCG A T HOOK3,AC110275.1 Ensembl:ENSG00000168172,Ensembl:ENSG00000254673 Protein coding,Protein coding 3'UTR,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1224629606 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16421262 RMVar_hsa_circ_104259,RMVar_hsa_circ_251659,RMVar_hsa_circ_79637,RMVar_hsa_circ_251721 52024 RMVar_ID_52024 Human_SNP_ID_360973017 A-to-I Human chr8 + 43021483 43021482 43021483 CCACCACCATGGCTGGCTAATTTTTGTAATTTAGTAGAGATGGTGTTTCACCATGTTGGCCAGGC CCACCACCATGGCTGGCTAATTTTTGTAATTT_GTAGAGATGGTGTTTCACCATGTTGGCCAGGC TA T HOOK3,AC110275.1 Ensembl:ENSG00000168172,Ensembl:ENSG00000254673 Protein coding,Protein coding 3'UTR,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1259744846 Functional Loss DEL dbSNP153 33..33 33 - - - Human_RBP_ID_179727 RMVar_hsa_circ_104259,RMVar_hsa_circ_251659,RMVar_hsa_circ_79637,RMVar_hsa_circ_251721 52025 RMVar_ID_52025 Human_SNP_ID_360973087 A-to-I Human chr8 + 43021733 43021733 43021733 CTCTGTCACCCAGGCTGGAGTGCAGTGGCGCGATCTCGGCTCACTGCAAGCTCCGCCTCCCGGGT CTCTGTCACCCAGGCTGGAGTGCAGTGGCGCGGTCTCGGCTCACTGCAAGCTCCGCCTCCCGGGT A G HOOK3,AC110275.1 Ensembl:ENSG00000168172,Ensembl:ENSG00000254673 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1192249615 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104259,RMVar_hsa_circ_251659,RMVar_hsa_circ_79637,RMVar_hsa_circ_251721 52026 RMVar_ID_52026 Human_SNP_ID_360973132 A-to-I Human chr8 + 43021876 43021876 43021876 ATTTTTTAGTAGAGACGGGGTTTCACCATGTTAGCCAGGATGGTCTCGATCTCCTGACCTCGTGA ATTTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGATGGTCTCGATCTCCTGACCTCGTGA A G HOOK3,AC110275.1 Ensembl:ENSG00000168172,Ensembl:ENSG00000254673 Protein coding,Protein coding 3'UTR,intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1416691432 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_179730 RMVar_hsa_circ_104259,RMVar_hsa_circ_251659,RMVar_hsa_circ_79637,RMVar_hsa_circ_251721 52027 RMVar_ID_52027 Human_SNP_ID_360973150 A-to-I Human chr8 + 43021921 43021921 43021921 TCGATCTCCTGACCTCGTGATCCACCCGCCTCAGCCTCCCAGAGTGCTGGGATTACAGGCGTGAG TCGATCTCCTGACCTCGTGATCCACCCGCCTCGGCCTCCCAGAGTGCTGGGATTACAGGCGTGAG A G HOOK3,AC110275.1 Ensembl:ENSG00000168172,Ensembl:ENSG00000254673 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1417127752 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104259,RMVar_hsa_circ_251659,RMVar_hsa_circ_79637,RMVar_hsa_circ_251721 52028 RMVar_ID_52028 Human_SNP_ID_360973606 A-to-I Human chr8 + 43023582 43023582 43023582 TCAAGCGATTCTCCTGCCTCATCCTCCCTAGTAGCTAGGATTACAGGCATCTGCCACCACGCCCA TCAAGCGATTCTCCTGCCTCATCCTCCCTAGTCGCTAGGATTACAGGCATCTGCCACCACGCCCA A C HOOK3,AC110275.1 Ensembl:ENSG00000168172,Ensembl:ENSG00000254673 Protein coding,Protein coding 3'UTR,intron GSE47997;GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line - 23474544,24183664,31158229 RNA-Seq:(High) rs1002884775 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104259,RMVar_hsa_circ_251659,RMVar_hsa_circ_79637,RMVar_hsa_circ_251721 52029 RMVar_ID_52029 Human_SNP_ID_360973608 A-to-I Human chr8 + 43023594 43023594 43023594 CCTGCCTCATCCTCCCTAGTAGCTAGGATTACAGGCATCTGCCACCACGCCCAGCTAATTTTTGT CCTGCCTCATCCTCCCTAGTAGCTAGGATTACTGGCATCTGCCACCACGCCCAGCTAATTTTTGT A T HOOK3,AC110275.1 Ensembl:ENSG00000168172,Ensembl:ENSG00000254673 Protein coding,Protein coding 3'UTR,intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells - 23474544,24183664 RNA-Seq:(High) rs956148900 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104259,RMVar_hsa_circ_251659,RMVar_hsa_circ_79637,RMVar_hsa_circ_251721 52030 RMVar_ID_52030 Human_SNP_ID_360973615 A-to-I Human chr8 + 43023614 43023614 43023614 AGCTAGGATTACAGGCATCTGCCACCACGCCCAGCTAATTTTTGTATTTTTACAAAATACAAAGA AGCTAGGATTACAGGCATCTGCCACCACGCCCGGCTAATTTTTGTATTTTTACAAAATACAAAGA A G HOOK3,AC110275.1 Ensembl:ENSG00000168172,Ensembl:ENSG00000254673 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs146282771 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104259,RMVar_hsa_circ_251659,RMVar_hsa_circ_79637,RMVar_hsa_circ_251721 52031 RMVar_ID_52031 Human_SNP_ID_360974594 A-to-I Human chr8 + 43028220 43028220 43028220 CTCTTTTAAAATTGATATTAGCTGGGCATGGTAGCTCATGCCTGTAGTCCCAGCTACTCCAGAGG CTCTTTTAAAATTGATATTAGCTGGGCATGGTGGCTCATGCCTGTAGTCCCAGCTACTCCAGAGG A G HOOK3,AC110275.1 Ensembl:ENSG00000168172,Ensembl:ENSG00000254673 Protein coding,Protein coding 3'UTR,intron GSE38233;GSE100210;GSE107867;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;ASD brains,frontal_cortex;ASD brains,temporal_cortex;Bronchiolar epithelium,BEP2D cell line - 24183664,29129909,30559470,30559470,31158229 RNA-Seq:(High) rs1019352964 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8221928 RMVar_hsa_circ_104259,RMVar_hsa_circ_251659,RMVar_hsa_circ_79637,RMVar_hsa_circ_251721 52032 RMVar_ID_52032 Human_SNP_ID_360974608 A-to-I Human chr8 + 43028279 43028279 43028279 CAGAGGTCGAGGCAGGAGCATCGCTTAAGCCCAGGAGGTTCAGGCTGCAGTAAGGTCTGATCACA CAGAGGTCGAGGCAGGAGCATCGCTTAAGCCCGGGAGGTTCAGGCTGCAGTAAGGTCTGATCACA A G HOOK3,AC110275.1 Ensembl:ENSG00000168172,Ensembl:ENSG00000254673 Protein coding,Protein coding 3'UTR,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1478342002 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8222324 RMVar_hsa_circ_104259,RMVar_hsa_circ_251659,RMVar_hsa_circ_79637,RMVar_hsa_circ_251721 52033 RMVar_ID_52033 Human_SNP_ID_360974823 A-to-I Human chr8 + 43029243 43029243 43029243 ACGATCTCGCCTCACTGCAACCTCCGCCTCCCAGGTTCAAGCTATTCTCCTGCCTCAGCCTCCCA ACGATCTCGCCTCACTGCAACCTCCGCCTCCCGGGTTCAAGCTATTCTCCTGCCTCAGCCTCCCA A G HOOK3,AC110275.1 Ensembl:ENSG00000168172,Ensembl:ENSG00000254673 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs61733908 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104259,RMVar_hsa_circ_251659,RMVar_hsa_circ_79637,RMVar_hsa_circ_251721 52034 RMVar_ID_52034 Human_SNP_ID_360974872 A-to-I Human chr8 + 43029422 43029422 43029422 TGCCCGCATTGGCCTCCTGAAGTGCTGGGATTACAGGCATGAGCCACTGCGCCCGGCCCAAATCT TGCCCGCATTGGCCTCCTGAAGTGCTGGGATTGCAGGCATGAGCCACTGCGCCCGGCCCAAATCT A G HOOK3,AC110275.1 Ensembl:ENSG00000168172,Ensembl:ENSG00000254673 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1378351768 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_104259,RMVar_hsa_circ_251659,RMVar_hsa_circ_79637,RMVar_hsa_circ_251721 52035 RMVar_ID_52035 Human_SNP_ID_360985717 A-to-I Human chr8 + 43069675 43069675 43069675 AAAAACTATCAAGTTTGGTAAGTTTGGAGTCTAGCTGTGTCTCCCAGGCTGGAGTGCAGTGGCAT AAAAACTATCAAGTTTGGTAAGTTTGGAGTCTTGCTGTGTCTCCCAGGCTGGAGTGCAGTGGCAT A T FNTA,AC110275.1 Ensembl:ENSG00000168522,Ensembl:ENSG00000254673 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1174447277 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8687427 RMVar_hsa_circ_58088,RMVar_hsa_circ_251733,RMVar_hsa_circ_275445,RMVar_hsa_circ_370250,RMVar_hsa_circ_251727,RMVar_hsa_circ_83085,RMVar_hsa_circ_376935,RMVar_hsa_circ_298437,RMVar_hsa_circ_301948,RMVar_hsa_circ_251729,RMVar_hsa_circ_251731,RMVar_hsa_circ_251732,RMVar_hsa_circ_251730,RMVar_hsa_circ_271995,RMVar_hsa_circ_278107,RMVar_hsa_circ_379033,RMVar_hsa_circ_251728,RMVar_hsa_circ_272615,RMVar_hsa_circ_265480,RMVar_hsa_circ_58585,RMVar_hsa_circ_251737,RMVar_hsa_circ_251739,RMVar_hsa_circ_251738,RMVar_hsa_circ_251743,RMVar_hsa_circ_275416,RMVar_hsa_circ_333923,RMVar_hsa_circ_342538,RMVar_hsa_circ_251742 52036 RMVar_ID_52036 Human_SNP_ID_360985826 A-to-I Human chr8 + 43070029 43070029 43070029 TAATCCCAGCAGTTTGGGAGGCTGAGGCGAGCAGATCACTTGAGTTCAGGAGTTTGAGACCAGCC TAATCCCAGCAGTTTGGGAGGCTGAGGCGAGCTGATCACTTGAGTTCAGGAGTTTGAGACCAGCC A T FNTA,AC110275.1 Ensembl:ENSG00000168522,Ensembl:ENSG00000254673 Protein coding,Protein coding intron,intron GSE38233;GSE107867 cultured B-cells;ASD brains,Fragile X samples from NIH NeuroBioBank - 24183664,30559470 RNA-Seq:(High) rs909115952 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58088,RMVar_hsa_circ_251733,RMVar_hsa_circ_275445,RMVar_hsa_circ_370250,RMVar_hsa_circ_251727,RMVar_hsa_circ_83085,RMVar_hsa_circ_376935,RMVar_hsa_circ_298437,RMVar_hsa_circ_301948,RMVar_hsa_circ_251729,RMVar_hsa_circ_251731,RMVar_hsa_circ_251732,RMVar_hsa_circ_251730,RMVar_hsa_circ_271995,RMVar_hsa_circ_278107,RMVar_hsa_circ_379033,RMVar_hsa_circ_251728,RMVar_hsa_circ_272615,RMVar_hsa_circ_265480,RMVar_hsa_circ_58585,RMVar_hsa_circ_251737,RMVar_hsa_circ_251739,RMVar_hsa_circ_251738,RMVar_hsa_circ_251743,RMVar_hsa_circ_275416,RMVar_hsa_circ_333923,RMVar_hsa_circ_342538,RMVar_hsa_circ_251742 52037 RMVar_ID_52037 Human_SNP_ID_360985842 A-to-I Human chr8 + 43070098 43070098 43070098 CAACATGGTGAATCCCCGTCTCTACTAAAAATACAGAAATTAGCCGGGTGTGGTGGCGTGCCTGT CAACATGGTGAATCCCCGTCTCTACTAAAAATGCAGAAATTAGCCGGGTGTGGTGGCGTGCCTGT A G FNTA,AC110275.1 Ensembl:ENSG00000168522,Ensembl:ENSG00000254673 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1165578746 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58088,RMVar_hsa_circ_251733,RMVar_hsa_circ_275445,RMVar_hsa_circ_370250,RMVar_hsa_circ_251727,RMVar_hsa_circ_83085,RMVar_hsa_circ_376935,RMVar_hsa_circ_298437,RMVar_hsa_circ_301948,RMVar_hsa_circ_251729,RMVar_hsa_circ_251731,RMVar_hsa_circ_251732,RMVar_hsa_circ_251730,RMVar_hsa_circ_271995,RMVar_hsa_circ_278107,RMVar_hsa_circ_379033,RMVar_hsa_circ_251728,RMVar_hsa_circ_272615,RMVar_hsa_circ_265480,RMVar_hsa_circ_58585,RMVar_hsa_circ_251737,RMVar_hsa_circ_251739,RMVar_hsa_circ_251738,RMVar_hsa_circ_251743,RMVar_hsa_circ_275416,RMVar_hsa_circ_333923,RMVar_hsa_circ_342538,RMVar_hsa_circ_251742 52038 RMVar_ID_52038 Human_SNP_ID_360987645 A-to-I Human chr8 + 43076691 43076691 43076691 CCTGAGGTTGGGAGTTCAAGACCAGCCTGACCAACGTGGAGAAACCCCATCTCTACTAAAAATAC CCTGAGGTTGGGAGTTCAAGACCAGCCTGACCGACGTGGAGAAACCCCATCTCTACTAAAAATAC A G FNTA,AC110275.1 Ensembl:ENSG00000168522,Ensembl:ENSG00000254673 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1409670879 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58088,RMVar_hsa_circ_275445,RMVar_hsa_circ_370250,RMVar_hsa_circ_251727,RMVar_hsa_circ_83085,RMVar_hsa_circ_376935,RMVar_hsa_circ_298437,RMVar_hsa_circ_251729,RMVar_hsa_circ_251731,RMVar_hsa_circ_251732,RMVar_hsa_circ_251730,RMVar_hsa_circ_271995,RMVar_hsa_circ_278107,RMVar_hsa_circ_379033,RMVar_hsa_circ_251728,RMVar_hsa_circ_265480,RMVar_hsa_circ_58585,RMVar_hsa_circ_251737,RMVar_hsa_circ_251738,RMVar_hsa_circ_251743,RMVar_hsa_circ_333923,RMVar_hsa_circ_342538,RMVar_hsa_circ_251745,RMVar_hsa_circ_330859,RMVar_hsa_circ_325215,RMVar_hsa_circ_251744 52039 RMVar_ID_52039 Human_SNP_ID_360987652 A-to-I Human chr8 + 43076716 43076715 43076717 CCTGACCAACGTGGAGAAACCCCATCTCTACTAAAAATACAAAATTAGCCAGGTGTGGTGGCGCA CCTGACCAACGTGGAGAAACCCCATCTCTACT__AAATACAAAATTAGCCAGGTGTGGTGGCGCA TAA T FNTA,AC110275.1 Ensembl:ENSG00000168522,Ensembl:ENSG00000254673 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1563329642 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_58088,RMVar_hsa_circ_275445,RMVar_hsa_circ_370250,RMVar_hsa_circ_251727,RMVar_hsa_circ_83085,RMVar_hsa_circ_376935,RMVar_hsa_circ_298437,RMVar_hsa_circ_251729,RMVar_hsa_circ_251731,RMVar_hsa_circ_251732,RMVar_hsa_circ_251730,RMVar_hsa_circ_271995,RMVar_hsa_circ_278107,RMVar_hsa_circ_379033,RMVar_hsa_circ_251728,RMVar_hsa_circ_265480,RMVar_hsa_circ_58585,RMVar_hsa_circ_251737,RMVar_hsa_circ_251738,RMVar_hsa_circ_251743,RMVar_hsa_circ_333923,RMVar_hsa_circ_342538,RMVar_hsa_circ_251745,RMVar_hsa_circ_330859,RMVar_hsa_circ_325215,RMVar_hsa_circ_251744 52040 RMVar_ID_52040 Human_SNP_ID_360987682 A-to-I Human chr8 + 43076827 43076827 43076827 TGAACCCAGGAAGTGGAGGTTGCAGTGAGCTGAGTTCACGCCATTGCACTCCAGCCTGGGCAACA TGAACCCAGGAAGTGGAGGTTGCAGTGAGCTGCGTTCACGCCATTGCACTCCAGCCTGGGCAACA A C FNTA,AC110275.1 Ensembl:ENSG00000168522,Ensembl:ENSG00000254673 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs961036507 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_58088,RMVar_hsa_circ_275445,RMVar_hsa_circ_370250,RMVar_hsa_circ_251727,RMVar_hsa_circ_83085,RMVar_hsa_circ_376935,RMVar_hsa_circ_298437,RMVar_hsa_circ_251729,RMVar_hsa_circ_251731,RMVar_hsa_circ_251732,RMVar_hsa_circ_251730,RMVar_hsa_circ_271995,RMVar_hsa_circ_278107,RMVar_hsa_circ_379033,RMVar_hsa_circ_251728,RMVar_hsa_circ_265480,RMVar_hsa_circ_58585,RMVar_hsa_circ_251737,RMVar_hsa_circ_251738,RMVar_hsa_circ_251743,RMVar_hsa_circ_333923,RMVar_hsa_circ_342538,RMVar_hsa_circ_251745,RMVar_hsa_circ_330859,RMVar_hsa_circ_325215,RMVar_hsa_circ_251744 52041 RMVar_ID_52041 Human_SNP_ID_361001556 A-to-I Human chr8 + 43130031 43130031 43130031 TTACATCTATTTTATTTGCAGGTCATATATCTAATAAGGAATTGATATCCAGTGTACATGTAGAA TTACATCTATTTTATTTGCAGGTCATATATCTGATAAGGAATTGATATCCAGTGTACATGTAGAA A G - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs11552313 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_1697055,Human_RBP_ID_2055498,Human_RBP_ID_9225489,Human_RBP_ID_16422891,Human_RBP_ID_18390873,Human_RBP_ID_21565423,Human_RBP_ID_26559161,Human_RBP_ID_27366363,Human_RBP_ID_27777414 52042 RMVar_ID_52042 Human_SNP_ID_361002127 A-to-I Human chr8 + 43132427 43132427 43132427 CACGAGGTCAGGAGTTCGAGACTAGGCTGGCCAAAATAGTGAAACCCCATCTCTACTAAAAATAC CACGAGGTCAGGAGTTCGAGACTAGGCTGGCCGAAATAGTGAAACCCCATCTCTACTAAAAATAC A G - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs914871827 Functional Loss SNV dbSNP153 33..33 33 - - - 52043 RMVar_ID_52043 Human_SNP_ID_361002129 A-to-I Human chr8 + 43132432 43132432 43132432 GGTCAGGAGTTCGAGACTAGGCTGGCCAAAATAGTGAAACCCCATCTCTACTAAAAATACAAAAA GGTCAGGAGTTCGAGACTAGGCTGGCCAAAATGGTGAAACCCCATCTCTACTAAAAATACAAAAA A G - - Other Unknown GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1304819747 Functional Loss SNV dbSNP153 33..33 33 - - - 52044 RMVar_ID_52044 Human_SNP_ID_361007448 A-to-I Human chr8 + 43152584 43152584 43152584 GAAATCCTTCTGCTTCAGCCTCTCAAGTAGCTAGGACTATAGGCGTGGACCATGACACCCAGCTA GAAATCCTTCTGCTTCAGCCTCTCAAGTAGCTGGGACTATAGGCGTGGACCATGACACCCAGCTA A G HGSNAT Ensembl:ENSG00000165102 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1310279295 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_41493,RMVar_hsa_circ_251751,RMVar_hsa_circ_95383,RMVar_hsa_circ_292157,RMVar_hsa_circ_309764,RMVar_hsa_circ_287171,RMVar_hsa_circ_251753,RMVar_hsa_circ_251754,RMVar_hsa_circ_251752 52045 RMVar_ID_52045 Human_SNP_ID_318942904 A-to-I Human chr7 + 45003634 45003634 45003634 TGTGCCTATAATCCCAGTTAGGAGGCTGAGGCAGGAGAATCTCTTGAACCCGGGAGGTGGAGGTT TGTGCCTATAATCCCAGTTAGGAGGCTGAGGCGGGAGAATCTCTTGAACCCGGGAGGTGGAGGTT A G CCM2 Ensembl:ENSG00000136280 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1341418972 Functional Loss SNV dbSNP153 33..33 33 - - - 52046 RMVar_ID_52046 Human_SNP_ID_318944410 A-to-I Human chr7 + 45009060 45009060 45009060 CACGGTGCTCACGCCTCTAATCCCAGCACTTTAGAAGGCCAAGGCAGGCAGATCACCTGAGATCA CACGGTGCTCACGCCTCTAATCCCAGCACTTTCGAAGGCCAAGGCAGGCAGATCACCTGAGATCA A C CCM2 Ensembl:ENSG00000136280 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1175018150 Functional Loss SNV dbSNP153 33..33 33 - - - 52047 RMVar_ID_52047 Human_SNP_ID_318944412 A-to-I Human chr7 + 45009068 45009068 45009068 TCACGCCTCTAATCCCAGCACTTTAGAAGGCCAAGGCAGGCAGATCACCTGAGATCAGAAGTTCA TCACGCCTCTAATCCCAGCACTTTAGAAGGCCCAGGCAGGCAGATCACCTGAGATCAGAAGTTCA A C CCM2 Ensembl:ENSG00000136280 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs543147570 Functional Loss SNV dbSNP153 33..33 33 - - - 52048 RMVar_ID_52048 Human_SNP_ID_318947248 A-to-I Human chr7 + 45019708 45019708 45019708 GGGCTCAAGCAATTCTCCTACCTTAGCCTCCCAAGTAGGTAGGACTACAGGCATGCACTATCTGG GGGCTCAAGCAATTCTCCTACCTTAGCCTCCCGAGTAGGTAGGACTACAGGCATGCACTATCTGG A G CCM2 Ensembl:ENSG00000136280 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1304244301 Functional Loss SNV dbSNP153 33..33 33 - - - 52049 RMVar_ID_52049 Human_SNP_ID_318947681 A-to-I Human chr7 + 45021449 45021449 45021449 AGCCAGGCATGGTGACACATGCCTGTAATCCCAGCTACTCGGGAGGCTGAGACAGGGAGAATTGC AGCCAGGCATGGTGACACATGCCTGTAATCCCGGCTACTCGGGAGGCTGAGACAGGGAGAATTGC A G CCM2 Ensembl:ENSG00000136280 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs940461895 Functional Loss SNV dbSNP153 33..33 33 - - - 52050 RMVar_ID_52050 Human_SNP_ID_318948065 A-to-I Human chr7 + 45022752 45022752 45022752 ATTGTATAGTGATGAAGTCTGGCTTTTATTTTATTTTTTGAGACGGAGTCTCATTCTGTTGGCCA ATTGTATAGTGATGAAGTCTGGCTTTTATTTTGTTTTTTGAGACGGAGTCTCATTCTGTTGGCCA A G CCM2 Ensembl:ENSG00000136280 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1007224695 Functional Loss SNV dbSNP153 33..33 33 - - - 52051 RMVar_ID_52051 Human_SNP_ID_318953345 A-to-I Human chr7 + 45043160 45043160 45043160 ATGCCCAGCTAATTTTTTATTTTGTAGAGATGAGGTCTCACTGTGTTGACCAGGCTGTCTTGAAC ATGCCCAGCTAATTTTTTATTTTGTAGAGATGCGGTCTCACTGTGTTGACCAGGCTGTCTTGAAC A C CCM2 Ensembl:ENSG00000136280 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs570025135 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_245030,RMVar_hsa_circ_295743 52052 RMVar_ID_52052 Human_SNP_ID_318958174 A-to-I Human chr7 + 45062705 45062705 45062705 AAAATTAGCCAGGCGTGGTGACACACACCTGTAGTACCAGCTACTCAGGAGGCTAAGGTGGGACA AAAATTAGCCAGGCGTGGTGACACACACCTGTGGTACCAGCTACTCAGGAGGCTAAGGTGGGACA A G CCM2 Ensembl:ENSG00000136280 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1262441876 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_245030,RMVar_hsa_circ_295743 52053 RMVar_ID_52053 Human_SNP_ID_318972131 A-to-I Human chr7 - 45110432 45110432 45110432 TCGATCTCCTGACCTCGTGATCTGCCCGCCTCAGCCTCCCAAAGTACTGGGATTACAGGCGTGAG TCGATCTCCTGACCTCGTGATCTGCCCGCCTCTGCCTCCCAAAGTACTGGGATTACAGGCGTGAG T A TBRG4 Ensembl:ENSG00000136270 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1348012793 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92636,RMVar_hsa_circ_245041,RMVar_hsa_circ_122474,RMVar_hsa_circ_245046 52054 RMVar_ID_52054 Human_SNP_ID_318972155 A-to-I Human chr7 - 45110502 45110502 45110502 CCACCACGCCCGGCTAATTTTTTTGTATTTTTAGTAGAGACGGTGTTTCACCGTGTTAGCCAGGA CCACCACGCCCGGCTAATTTTTTTGTATTTTTGGTAGAGACGGTGTTTCACCGTGTTAGCCAGGA T C TBRG4 Ensembl:ENSG00000136270 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs568447003 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92636,RMVar_hsa_circ_245041,RMVar_hsa_circ_122474,RMVar_hsa_circ_245046 52055 RMVar_ID_52055 Human_SNP_ID_318972156 A-to-I Human chr7 - 45110502 45110502 45110502 CCACCACGCCCGGCTAATTTTTTTGTATTTTTAGTAGAGACGGTGTTTCACCGTGTTAGCCAGGA CCACCACGCCCGGCTAATTTTTTTGTATTTTTCGTAGAGACGGTGTTTCACCGTGTTAGCCAGGA T G TBRG4 Ensembl:ENSG00000136270 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs568447003 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92636,RMVar_hsa_circ_245041,RMVar_hsa_circ_122474,RMVar_hsa_circ_245046 52056 RMVar_ID_52056 Human_SNP_ID_318972182 A-to-I Human chr7 - 45110558 45110558 45110558 CGGCTCACTTCAAGCTCTGCCTCACCCTCCCTAGTAGCTGGGACTACAGGTGCCCGCCACCACGC CGGCTCACTTCAAGCTCTGCCTCACCCTCCCTTGTAGCTGGGACTACAGGTGCCCGCCACCACGC T A TBRG4 Ensembl:ENSG00000136270 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1216083876 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16167589 RMVar_hsa_circ_92636,RMVar_hsa_circ_245041,RMVar_hsa_circ_122474,RMVar_hsa_circ_245046 52057 RMVar_ID_52057 Human_SNP_ID_318972342 A-to-I Human chr7 - 45111036 45111036 45111036 GGGAGGCTGAGGTTGCAGTGACTCGAGATCGCAGCATTGCACTCCAGTCTGGGCGACAGAGCGAG GGGAGGCTGAGGTTGCAGTGACTCGAGATCGCCGCATTGCACTCCAGTCTGGGCGACAGAGCGAG T G TBRG4 Ensembl:ENSG00000136270 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs926386871 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16167614 RMVar_hsa_circ_92636,RMVar_hsa_circ_245041,RMVar_hsa_circ_122474,RMVar_hsa_circ_245046 52058 RMVar_ID_52058 Human_SNP_ID_319128757 A-to-I Human chr7 - 45742102 45742102 45742102 TGAGGCAGGAGGATGGTTTGAGCCTGAAAGGCAGAGGTTGTAGTGAGCTGAGATTGTACCACCAC TGAGGCAGGAGGATGGTTTGAGCCTGAAAGGCCGAGGTTGTAGTGAGCTGAGATTGTACCACCAC T G SEPTIN7P2 Ensembl:ENSG00000214765 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1197143591 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8272212 RMVar_hsa_circ_33010,RMVar_hsa_circ_288572,RMVar_hsa_circ_11814,RMVar_hsa_circ_115309,RMVar_hsa_circ_245062,RMVar_hsa_circ_298590,RMVar_hsa_circ_349989,RMVar_hsa_circ_267751,RMVar_hsa_circ_42483,RMVar_hsa_circ_245064,RMVar_hsa_circ_5530 52059 RMVar_ID_52059 Human_SNP_ID_319128972 A-to-I Human chr7 - 45743404 45743386 45743404 TGGCTAACTGCAATCTCCACTTCCCCGCTTCAAGCAATTCTCCTGCCTCAGCCTCCCGAATAGCT TGGCTAACTGCAATCTCCACTTCCCCGCTTCA__________________GCCTCCCGAATAGCT CTGAGGCAGGAGAATTGCT C SEPTIN7P2 Ensembl:ENSG00000214765 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1275754389 Functional Loss DEL dbSNP153 33..50 33 - - - RMVar_hsa_circ_33010,RMVar_hsa_circ_288572,RMVar_hsa_circ_11814,RMVar_hsa_circ_115309,RMVar_hsa_circ_245062,RMVar_hsa_circ_298590,RMVar_hsa_circ_349989,RMVar_hsa_circ_267751,RMVar_hsa_circ_42483,RMVar_hsa_circ_245064,RMVar_hsa_circ_5530 52060 RMVar_ID_52060 Human_SNP_ID_319145002 A-to-I Human chr7 + 45812176 45812176 45812176 AGACGCCCCTGGGAGGCAACAGCGGGGCCTGCAGATGCTTTCTGCTGCCAGAGCTGGGACTGTAC AGACGCCCCTGGGAGGCAACAGCGGGGCCTGCGGATGCTTTCTGCTGCCAGAGCTGGGACTGTAC A G GTF2IP13 Ensembl:ENSG00000272556 Pseudogene exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs969215746 Functional Loss SNV dbSNP153 33..33 33 - - - 52061 RMVar_ID_52061 Human_SNP_ID_319145800 A-to-I Human chr7 + 45814103 45814103 45814103 GGACGCCCCTGGGAGGCAACAGTGGGGCCTGCAGACGCTCTTCTCCTGCCAGAGCTGGGACTGTA GGACGCCCCTGGGAGGCAACAGTGGGGCCTGCGGACGCTCTTCTCCTGCCAGAGCTGGGACTGTA A G GTF2IP13 Ensembl:ENSG00000272556 Pseudogene exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1266629972 Functional Loss SNV dbSNP153 33..33 33 - - - 52062 RMVar_ID_52062 Human_SNP_ID_319145842 A-to-I Human chr7 + 45814220 45814220 45814220 CGGGGTCTACAAACGCCGGCGGGAGCTGAGCCAAAAGAGCTTGCTTGCTGGGAGGCAGGGGGTGG CGGGGTCTACAAACGCCGGCGGGAGCTGAGCCGAAAGAGCTTGCTTGCTGGGAGGCAGGGGGTGG A G GTF2IP13 Ensembl:ENSG00000272556 Pseudogene exon GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs943795751 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_5624160,Human_RBP_ID_17429677 52063 RMVar_ID_52063 Human_SNP_ID_319692512 A-to-I Human chr7 - 47962566 47962566 47962566 CAGGTGTGTGCCACTGCGCCCAGCTAATTTTTATATTGTTTTGTAGATATGAGGTTTTGTACGTT CAGGTGTGTGCCACTGCGCCCAGCTAATTTTTGTATTGTTTTGTAGATATGAGGTTTTGTACGTT T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs954903536 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7743588,Human_RBP_ID_21509423 52064 RMVar_ID_52064 Human_SNP_ID_319692513 A-to-I Human chr7 - 47962566 47962566 47962566 CAGGTGTGTGCCACTGCGCCCAGCTAATTTTTATATTGTTTTGTAGATATGAGGTTTTGTACGTT CAGGTGTGTGCCACTGCGCCCAGCTAATTTTTCTATTGTTTTGTAGATATGAGGTTTTGTACGTT T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs954903536 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_7743588,Human_RBP_ID_21509423 52065 RMVar_ID_52065 Human_SNP_ID_319692979 A-to-I Human chr7 - 47964213 47964213 47964213 CCACCACACCCAGCTAATTTTCAATTTTTCATAGAGACAGGGTCTCACTGTGTTGTCCAGGCTGG CCACCACACCCAGCTAATTTTCAATTTTTCATGGAGACAGGGTCTCACTGTGTTGTCCAGGCTGG T C HUS1 Ensembl:ENSG00000136273 Protein coding 3'UTR GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1263228257 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_685359,Human_RBP_ID_7743618,Human_RBP_ID_16169928,Human_RBP_ID_18451707 52066 RMVar_ID_52066 Human_SNP_ID_319727612 A-to-I Human chr7 + 48103928 48103927 48103928 CAACAGGGACATTTTTTTTTTGTTTAAAAAACAAAGATGGTTGGCCGGGCGCGGTGGCTCACACC CAACAGGGACATTTTTTTTTTGTTTAAAAAAC_AAGATGGTTGGCCGGGCGCGGTGGCTCACACC CA C UPP1 Ensembl:ENSG00000183696 Protein coding intron GSE107867 ASD brains,cerebellum - 30559470 RNA-Seq:(High) rs1377769844 Functional Loss DEL dbSNP153 33..33 33 - - - 52067 RMVar_ID_52067 Human_SNP_ID_319727625 A-to-I Human chr7 + 48103958 48103958 48103958 ACAAAGATGGTTGGCCGGGCGCGGTGGCTCACACCTGTAATCCCAGCACATTGGGAGGCCGAGGC ACAAAGATGGTTGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACATTGGGAGGCCGAGGC A G UPP1 Ensembl:ENSG00000183696 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1258258936 Functional Loss SNV dbSNP153 33..33 33 - - - 52068 RMVar_ID_52068 Human_SNP_ID_319727686 A-to-I Human chr7 + 48104124 48104124 48104124 TCTGTAGTCCCAGCTGCTGGTGAGGCTGAGGCAGGAGAATCGCTTGAACCCGGGAGGCGGAGGTT TCTGTAGTCCCAGCTGCTGGTGAGGCTGAGGCGGGAGAATCGCTTGAACCCGGGAGGCGGAGGTT A G UPP1 Ensembl:ENSG00000183696 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs1260590345 Functional Loss SNV dbSNP153 33..33 33 - - - 52069 RMVar_ID_52069 Human_SNP_ID_319728285 A-to-I Human chr7 + 48106491 48106491 48106491 CGGCACAATGCCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTCTCACCATGTTGGCCAGGC CGGCACAATGCCTGGCTAATTTTTGTATTTTTTGTAGAGATGGGGTCTCACCATGTTGGCCAGGC A T UPP1 Ensembl:ENSG00000183696 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1265255757 Functional Loss SNV dbSNP153 33..33 33 - - - 52070 RMVar_ID_52070 Human_SNP_ID_319728303 A-to-I Human chr7 + 48106572 48106572 48106572 ACCTCAGGTGATCTGCTCGTCTTGGCCTCCCAAAGTGCTTGGGATTACAGGCGTGGGCCACTGCA ACCTCAGGTGATCTGCTCGTCTTGGCCTCCCATAGTGCTTGGGATTACAGGCGTGGGCCACTGCA A T UPP1 Ensembl:ENSG00000183696 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229,31158229 RNA-Seq:(High) rs149757934 Functional Loss SNV dbSNP153 33..33 33 - - - 52071 RMVar_ID_52071 Human_SNP_ID_320318495 A-to-I Human chr7 - 50438487 50438487 50438487 ACAATATCACCACAAACTTAGTGACTTTAAACAACACACATTAATGACCTTGTAGTTTCTTTCAG ACAATATCACCACAAACTTAGTGACTTTAAACCACACACATTAATGACCTTGTAGTTTCTTTCAG T G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs532975396 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17425769,Human_RBP_ID_18101581,Human_RBP_ID_27769006 52072 RMVar_ID_52072 Human_SNP_ID_320321009 A-to-I Human chr7 - 50448023 50448023 50448023 ATAAGAAAACTGAAGAACCAGCTGGGCGCGGTAGCTCACGCCTGTAATCCCAGCACTTTGGGAGG ATAAGAAAACTGAAGAACCAGCTGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGG T C FIGNL1 Ensembl:ENSG00000132436 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs943566081 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_866664,Human_Splice_Rec_866665,Human_Splice_Rec_866668,Human_Splice_Rec_866669,Human_Splice_Rec_866676,Human_Splice_Rec_866677,Human_Splice_Rec_866684,Human_Splice_Rec_866685 RMVar_hsa_circ_4507,RMVar_hsa_circ_100095,RMVar_hsa_circ_245127 52073 RMVar_ID_52073 Human_SNP_ID_320491822 A-to-I Human chr7 - 51124863 51124863 51124863 TGAGCTGAGGTCACGCCGCTGCACTCTAGCCTAGGCAATAGAGTGAGACTCTGTCAAAGAAAAAA TGAGCTGAGGTCACGCCGCTGCACTCTAGCCTGGGCAATAGAGTGAGACTCTGTCAAAGAAAAAA T C COBL Ensembl:ENSG00000106078 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1240924898 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_59475,RMVar_hsa_circ_76442,RMVar_hsa_circ_53550,RMVar_hsa_circ_367392,RMVar_hsa_circ_245159 52074 RMVar_ID_52074 Human_SNP_ID_320504950 A-to-I Human chr7 - 51178788 51178788 51178788 CCTGACCAGCTTGGAGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCCGGGCATGGTGGCAG CCTGACCAGCTTGGAGAAACCCCGTCTCTACTGAAAATACAAAAATTAGCCGGGCATGGTGGCAG T C COBL Ensembl:ENSG00000106078 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1279438181 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_14327,RMVar_hsa_circ_59475,RMVar_hsa_circ_76442,RMVar_hsa_circ_53550,RMVar_hsa_circ_72689,RMVar_hsa_circ_245159 52075 RMVar_ID_52075 Human_SNP_ID_320981944 A-to-I Human chr7 + 53002761 53002761 53002761 GTAGAGAAGCTAAAAGGAGAACTTGAAAGTTCAGACCAGGTGAGGCAGCACACCTCACATTTGGA GTAGAGAAGCTAAAAGGAGAACTTGAAAGTTCCGACCAGGTGAGGCAGCACACCTCACATTTGGA A C AC074397.1 Ensembl:ENSG00000223970 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1202280246 Functional Loss SNV dbSNP153 33..33 33 - - - 52076 RMVar_ID_52076 Human_SNP_ID_321618130 A-to-I Human chr7 - 55454933 55454933 55454933 CTCTTGCCTGATTGCCTTGGCCAGAACTTCCAATACTGTGTTGAATAGGAGTGATGAGAGAGGGC CTCTTGCCTGATTGCCTTGGCCAGAACTTCCAGTACTGTGTTGAATAGGAGTGATGAGAGAGGGC T C VOPP1 Ensembl:ENSG00000154978 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1161231623 Functional Loss SNV dbSNP153 33..33 33 - - - 52077 RMVar_ID_52077 Human_SNP_ID_321618131 A-to-I Human chr7 - 55454934 55454934 55454934 TCTCTTGCCTGATTGCCTTGGCCAGAACTTCCAATACTGTGTTGAATAGGAGTGATGAGAGAGGG TCTCTTGCCTGATTGCCTTGGCCAGAACTTCCCATACTGTGTTGAATAGGAGTGATGAGAGAGGG T G VOPP1 Ensembl:ENSG00000154978 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1443609860 Functional Loss SNV dbSNP153 33..33 33 - - - 52078 RMVar_ID_52078 Human_SNP_ID_321618135 A-to-I Human chr7 - 55454973 55454965 55454973 TCTTTTCCTAATTGAATACGCTTTATTTCTTTATTTCTTTCTCTTGCCTGATTGCCTTGGCCAGA TCTTTTCCTAATTGAATACGCTTTATTTCTTT________CTCTTGCCTGATTGCCTTGGCCAGA GAAAGAAAT G VOPP1 Ensembl:ENSG00000154978 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1210366049 Functional Loss DEL dbSNP153 33..40 33 - - - Human_RBP_ID_3848691 52079 RMVar_ID_52079 Human_SNP_ID_321618138 A-to-I Human chr7 - 55454973 55454973 55454973 TCTTTTCCTAATTGAATACGCTTTATTTCTTTATTTCTTTCTCTTGCCTGATTGCCTTGGCCAGA TCTTTTCCTAATTGAATACGCTTTATTTCTTTCTTTCTTTCTCTTGCCTGATTGCCTTGGCCAGA T G VOPP1 Ensembl:ENSG00000154978 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs968913206 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3848691 52080 RMVar_ID_52080 Human_SNP_ID_321618712 A-to-I Human chr7 - 55457483 55457483 55457483 TGACCACTAAATCAGACTACTAAATCCCCACTACTGGGTATTTACCCAAAAGACAGGAAATCGGT TGACCACTAAATCAGACTACTAAATCCCCACTGCTGGGTATTTACCCAAAAGACAGGAAATCGGT T C VOPP1 Ensembl:ENSG00000154978 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1315193264 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17313290 52081 RMVar_ID_52081 Human_SNP_ID_321618713 A-to-I Human chr7 - 55457483 55457483 55457483 TGACCACTAAATCAGACTACTAAATCCCCACTACTGGGTATTTACCCAAAAGACAGGAAATCGGT TGACCACTAAATCAGACTACTAAATCCCCACTCCTGGGTATTTACCCAAAAGACAGGAAATCGGT T G VOPP1 Ensembl:ENSG00000154978 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1315193264 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17313290 52082 RMVar_ID_52082 Human_SNP_ID_321618730 A-to-I Human chr7 - 55457560 55457560 55457560 ACTCTTACACACTGTTGGTGGATATATAAATCACTACAGTCATTATGGAAAACAGTATAGAGGTT ACTCTTACACACTGTTGGTGGATATATAAATCCCTACAGTCATTATGGAAAACAGTATAGAGGTT T G VOPP1 Ensembl:ENSG00000154978 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1448183735 Functional Loss SNV dbSNP153 33..33 33 - - - 52083 RMVar_ID_52083 Human_SNP_ID_321618731 A-to-I Human chr7 - 55457567 55457567 55457567 AAAGGGAACTCTTACACACTGTTGGTGGATATATAAATCACTACAGTCATTATGGAAAACAGTAT AAAGGGAACTCTTACACACTGTTGGTGGATATGTAAATCACTACAGTCATTATGGAAAACAGTAT T C VOPP1 Ensembl:ENSG00000154978 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1213970487 Functional Loss SNV dbSNP153 33..33 33 - - - 52084 RMVar_ID_52084 Human_SNP_ID_321618777 A-to-I Human chr7 - 55457708 55457708 55457708 GCCAAGTATATGAAAAAATGTTTAACATCACTAGCCATCAGGGAAATGCATATCAAAACCACAAT GCCAAGTATATGAAAAAATGTTTAACATCACTGGCCATCAGGGAAATGCATATCAAAACCACAAT T C VOPP1 Ensembl:ENSG00000154978 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs1323035347 Functional Loss SNV dbSNP153 33..33 33 - - - 52085 RMVar_ID_52085 Human_SNP_ID_321618834 A-to-I Human chr7 - 55457921 55457918 55457922 ACTATATTAAGCTAAAAAGATTCTGCAAAACAAAGGAAACAGTCAACAGAGTGAAGAGACAATCT ACTATATTAAGCTAAAAAGATTCTGCAAAAC____GAAACAGTCAACAGAGTGAAGAGACAATCT CCTTT C VOPP1 Ensembl:ENSG00000154978 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line - 24183664,31158229 RNA-Seq:(High) rs761265104 Functional Loss DEL dbSNP153 32..35 33 - - - 52086 RMVar_ID_52086 Human_SNP_ID_321618863 A-to-I Human chr7 - 55458124 55458124 55458124 GAAAACTGAATATTCATCTGCAAAATAATGAAACTAGACCCCTAATGTCTCACCATACACAAAAA GAAAACTGAATATTCATCTGCAAAATAATGAATCTAGACCCCTAATGTCTCACCATACACAAAAA T A VOPP1 Ensembl:ENSG00000154978 Protein coding intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs997600165 Functional Loss SNV dbSNP153 33..33 33 - - - 52087 RMVar_ID_52087 Human_SNP_ID_321618865 A-to-I Human chr7 - 55458134 55458134 55458134 AGGGTACTGAGAAAACTGAATATTCATCTGCAAAATAATGAAACTAGACCCCTAATGTCTCACCA AGGGTACTGAGAAAACTGAATATTCATCTGCAGAATAATGAAACTAGACCCCTAATGTCTCACCA T C VOPP1 Ensembl:ENSG00000154978 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs188034642 Functional Loss SNV dbSNP153 33..33 33 - - - 52088 RMVar_ID_52088 Human_SNP_ID_321618890 A-to-I Human chr7 - 55458247 55458247 55458247 GACCAATGGAACAGAATAGAAAACCCAGAAATAAATACATATATTTACCACCAACTGATTTTCAC GACCAATGGAACAGAATAGAAAACCCAGAAATGAATACATATATTTACCACCAACTGATTTTCAC T C VOPP1 Ensembl:ENSG00000154978 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs972185882 Functional Loss SNV dbSNP153 33..33 33 - - - 52089 RMVar_ID_52089 Human_SNP_ID_321618891 A-to-I Human chr7 - 55458249 55458249 55458249 CAGACCAATGGAACAGAATAGAAAACCCAGAAATAAATACATATATTTACCACCAACTGATTTTC CAGACCAATGGAACAGAATAGAAAACCCAGAAGTAAATACATATATTTACCACCAACTGATTTTC T C VOPP1 Ensembl:ENSG00000154978 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1175615807 Functional Loss SNV dbSNP153 33..33 33 - - - 52090 RMVar_ID_52090 Human_SNP_ID_321618900 A-to-I Human chr7 - 55458284 55458284 55458284 ACCCAAAGAGCATAGTATTGATATAAACAGACACACAGACCAATGGAACAGAATAGAAAACCCAG ACCCAAAGAGCATAGTATTGATATAAACAGACGCACAGACCAATGGAACAGAATAGAAAACCCAG T C VOPP1 Ensembl:ENSG00000154978 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1020956443 Functional Loss SNV dbSNP153 33..33 33 - - - 52091 RMVar_ID_52091 Human_SNP_ID_321618914 A-to-I Human chr7 - 55458348 55458348 55458348 AGCAAAAAAGAAAAAGCTGGAAGCATCACACTACTTAACTTCAAAACATTACAGGGCTATGGTAA AGCAAAAAAGAAAAAGCTGGAAGCATCACACTGCTTAACTTCAAAACATTACAGGGCTATGGTAA T C VOPP1 Ensembl:ENSG00000154978 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1301435447 Functional Loss SNV dbSNP153 33..33 33 - - - 52092 RMVar_ID_52092 Human_SNP_ID_321618917 A-to-I Human chr7 - 55458359 55458359 55458359 AAGCAACCCTGAGCAAAAAAGAAAAAGCTGGAAGCATCACACTACTTAACTTCAAAACATTACAG AAGCAACCCTGAGCAAAAAAGAAAAAGCTGGAGGCATCACACTACTTAACTTCAAAACATTACAG T C VOPP1 Ensembl:ENSG00000154978 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1399230618 Functional Loss SNV dbSNP153 33..33 33 - - - 52093 RMVar_ID_52093 Human_SNP_ID_321618923 A-to-I Human chr7 - 55458390 55458389 55458390 ATATGAAATCAAAAAAGAATCAGAATAGCCAAAGCAACCCTGAGCAAAAAAGAAAAAGCTGGAAG ATATGAAATCAAAAAAGAATCAGAATAGCCAA_GCAACCCTGAGCAAAAAAGAAAAAGCTGGAAG CT C VOPP1 Ensembl:ENSG00000154978 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs1173977363 Functional Loss DEL dbSNP153 33..33 33 - - - 52094 RMVar_ID_52094 Human_SNP_ID_321618947 A-to-I Human chr7 - 55458483 55458483 55458483 ATGTTTACCCAAAGTAAACTTGATTCAAAGCAATCTCTATCAAAATACTATTGTCATTTGTCACA ATGTTTACCCAAAGTAAACTTGATTCAAAGCAGTCTCTATCAAAATACTATTGTCATTTGTCACA T C VOPP1 Ensembl:ENSG00000154978 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1434381339 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18883916 52095 RMVar_ID_52095 Human_SNP_ID_321618974 A-to-I Human chr7 - 55458604 55458604 55458604 CTCGGATCTAACCAAAAAGGTGAAAGGTCTCTACAAGGGAAACTACAAAACACTAATGAAAGAAA CTCGGATCTAACCAAAAAGGTGAAAGGTCTCTGCAAGGGAAACTACAAAACACTAATGAAAGAAA T C VOPP1 Ensembl:ENSG00000154978 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1414386612 Functional Loss SNV dbSNP153 33..33 33 - - - 52096 RMVar_ID_52096 Human_SNP_ID_321619031 A-to-I Human chr7 - 55458907 55458907 55458907 TGCCCACATTCACCACTCTTATTCAACATAGCACTAGAAGTTCTAGCCAGAGCAATCAGGCAAGA TGCCCACATTCACCACTCTTATTCAACATAGCTCTAGAAGTTCTAGCCAGAGCAATCAGGCAAGA T A VOPP1 Ensembl:ENSG00000154978 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1028075547 Functional Loss SNV dbSNP153 33..33 33 - - - 52097 RMVar_ID_52097 Human_SNP_ID_321619033 A-to-I Human chr7 - 55458914 55458914 55458914 AGCAGGATGCCCACATTCACCACTCTTATTCAACATAGCACTAGAAGTTCTAGCCAGAGCAATCA AGCAGGATGCCCACATTCACCACTCTTATTCAGCATAGCACTAGAAGTTCTAGCCAGAGCAATCA T C VOPP1 Ensembl:ENSG00000154978 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs952122329 Functional Loss SNV dbSNP153 33..33 33 - - - 52098 RMVar_ID_52098 Human_SNP_ID_321619047 A-to-I Human chr7 - 55458961 55458961 55458961 CTAAATGGGGAAAAGCTGAAAGACCTTCTTCTAAAAACTGGAACCAGAGCAGGATGCCCACATTC CTAAATGGGGAAAAGCTGAAAGACCTTCTTCTTAAAACTGGAACCAGAGCAGGATGCCCACATTC T A VOPP1 Ensembl:ENSG00000154978 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs1279634050 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22324162 52099 RMVar_ID_52099 Human_SNP_ID_321619064 A-to-I Human chr7 - 55459065 55459063 55459066 GTATCCCTTCATGATAAAAAAAAACTCTCAACAAATTAGACATACAAGGAACATACCTCAACATA GTATCCCTTCATGATAAAAAAAAACTCTCAA___ATTAGACATACAAGGAACATACCTCAACATA TTTG T VOPP1 Ensembl:ENSG00000154978 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1441458671 Functional Loss DEL dbSNP153 32..34 33 - - - 52100 RMVar_ID_52100 Human_SNP_ID_321619065 A-to-I Human chr7 - 55459065 55459065 55459065 GTATCCCTTCATGATAAAAAAAAACTCTCAACAAATTAGACATACAAGGAACATACCTCAACATA GTATCCCTTCATGATAAAAAAAAACTCTCAACTAATTAGACATACAAGGAACATACCTCAACATA T A VOPP1 Ensembl:ENSG00000154978 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs989793227 Functional Loss SNV dbSNP153 33..33 33 - - - 52101 RMVar_ID_52101 Human_SNP_ID_321619090 A-to-I Human chr7 - 55459133 55459133 55459133 ATCAGTGGAATGAAGGAAAAAACTTTATGATTATCTCAATAGATGCAGAAAATTGTTTGATAAAT ATCAGTGGAATGAAGGAAAAAACTTTATGATTGTCTCAATAGATGCAGAAAATTGTTTGATAAAT T C VOPP1 Ensembl:ENSG00000154978 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs963822123 Functional Loss SNV dbSNP153 33..33 33 - - - 52102 RMVar_ID_52102 Human_SNP_ID_321619112 A-to-I Human chr7 - 55459275 55459275 55459275 AACACAGGCATAAAAATCATCAACAAAATGCTAGCAAGCTGAATTCAACAGTACACCAAAAAGAT AACACAGGCATAAAAATCATCAACAAAATGCTGGCAAGCTGAATTCAACAGTACACCAAAAAGAT T C VOPP1 Ensembl:ENSG00000154978 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1002627631 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18883917 52103 RMVar_ID_52103 Human_SNP_ID_321619118 A-to-I Human chr7 - 55459332 55459329 55459333 ACCAAAACCAGAGAAGGACACAACGAAAAAGAAAGCTACAGGCCAATATCCCTGATGAACACAGG ACCAAAACCAGAGAAGGACACAACGAAAAAG____CTACAGGCCAATATCCCTGATGAACACAGG GCTTT G VOPP1 Ensembl:ENSG00000154978 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line - 31158229 RNA-Seq:(High) rs1186072068 Functional Loss DEL dbSNP153 32..35 33 - - - 52104 RMVar_ID_52104 Human_SNP_ID_321619132 A-to-I Human chr7 - 55459420 55459420 55459420 AACACCAATTCTTCACAAACTGTTTAAAAACAATTGAAGAGGAGGGAATTTTTCCTAACTCATTC AACACCAATTCTTCACAAACTGTTTAAAAACAGTTGAAGAGGAGGGAATTTTTCCTAACTCATTC T C VOPP1 Ensembl:ENSG00000154978 Protein coding intron GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line - 24183664,31158229 RNA-Seq:(High) rs989122639 Functional Loss SNV dbSNP153 33..33 33 - - - 52105 RMVar_ID_52105 Human_SNP_ID_321619175 A-to-I Human chr7 - 55459621 55459621 55459621 CAACAAAATGGAAAACCTAGAGGAAATGGGTAAATTCCTGGACACATACAACCTTCCAAGATTGA CAACAAAATGGAAAACCTAGAGGAAATGGGTACATTCCTGGACACATACAACCTTCCAAGATTGA T G VOPP1 Ensembl:ENSG00000154978 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1191187547 Functional Loss SNV dbSNP153 33..33 33 - - - 52106 RMVar_ID_52106 Human_SNP_ID_321686974 A-to-I Human chr7 - 55736104 55736096 55736105 TTTTAAAGTAGACCTAGTGGTGGCTCATGCCTATAATCCCAGCACTCTGGGAGGCCAAGGTTTCA TTTTAAAGTAGACCTAGTGGTGGCTCATGCC_________AGCACTCTGGGAGGCCAAGGTTTCA TGGGATTATA T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1472656338 Functional Loss DEL dbSNP153 32..40 33 - - - Human_RBP_ID_16179257,Human_RBP_ID_21513806,Human_RBP_ID_23198008 52107 RMVar_ID_52107 Human_SNP_ID_321694765 A-to-I Human chr7 + 55764339 55764339 55764339 GGGCGTGGTGATAGGCGCCTGTAATCCCAGCTACCCAGGAGGCTGAGGGAGGAAAATCACTGGAA GGGCGTGGTGATAGGCGCCTGTAATCCCAGCTTCCCAGGAGGCTGAGGGAGGAAAATCACTGGAA A T - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1256794727 Functional Loss SNV dbSNP153 33..33 33 - - - 52108 RMVar_ID_52108 Human_SNP_ID_321695872 A-to-I Human chr7 + 55767949 55767949 55767949 AAAAAATTAGCTGGAAGTGGTGATGGGTGCCTATCATTGCAGCTACTTAGGAGGCTGAGGCATGA AAAAAATTAGCTGGAAGTGGTGATGGGTGCCTCTCATTGCAGCTACTTAGGAGGCTGAGGCATGA A C PSPHP1 Ensembl:ENSG00000226278 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917150107 Functional Loss SNV dbSNP153 33..33 33 - - - 52109 RMVar_ID_52109 Human_SNP_ID_321695873 A-to-I Human chr7 + 55767949 55767949 55767949 AAAAAATTAGCTGGAAGTGGTGATGGGTGCCTATCATTGCAGCTACTTAGGAGGCTGAGGCATGA AAAAAATTAGCTGGAAGTGGTGATGGGTGCCTGTCATTGCAGCTACTTAGGAGGCTGAGGCATGA A G PSPHP1 Ensembl:ENSG00000226278 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs917150107 Functional Loss SNV dbSNP153 33..33 33 - - - 52110 RMVar_ID_52110 Human_SNP_ID_321695878 A-to-I Human chr7 + 55767965 55767965 55767965 GTGGTGATGGGTGCCTATCATTGCAGCTACTTAGGAGGCTGAGGCATGAGAATCAGTCAAACCCA GTGGTGATGGGTGCCTATCATTGCAGCTACTTGGGAGGCTGAGGCATGAGAATCAGTCAAACCCA A G PSPHP1 Ensembl:ENSG00000226278 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs949786415 Functional Loss SNV dbSNP153 33..33 33 - - - 52111 RMVar_ID_52111 Human_SNP_ID_321696470 A-to-I Human chr7 + 55770267 55770267 55770267 ACAGCTCACTGCAACCTCGAACTCCCAGGCTCAAGTGATCCTTCTGCCTCAGCGTCCTGAGTAGC ACAGCTCACTGCAACCTCGAACTCCCAGGCTCCAGTGATCCTTCTGCCTCAGCGTCCTGAGTAGC A C PSPHP1 Ensembl:ENSG00000226278 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1339868140 Functional Loss SNV dbSNP153 33..33 33 - - - 52112 RMVar_ID_52112 Human_SNP_ID_321696499 A-to-I Human chr7 + 55770371 55770371 55770371 TAATTTTTTTTATAGAGATGGGGTCTCACTATATTGCCCATGCTGGTCTCAAACTCTGGCCTCAA TAATTTTTTTTATAGAGATGGGGTCTCACTATGTTGCCCATGCTGGTCTCAAACTCTGGCCTCAA A G PSPHP1 Ensembl:ENSG00000226278 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1420125841 Functional Loss SNV dbSNP153 33..33 33 - - - 52113 RMVar_ID_52113 Human_SNP_ID_321697244 A-to-I Human chr7 + 55772875 55772875 55772875 AAATCATTTCTCCTCCGGGTGCTGTGGCTCATACCTATAATCCCAGCACCTTGGGAGGCCGAAGT AAATCATTTCTCCTCCGGGTGCTGTGGCTCATGCCTATAATCCCAGCACCTTGGGAGGCCGAAGT A G PSPHP1 Ensembl:ENSG00000226278 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1012191305 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18520586 52114 RMVar_ID_52114 Human_SNP_ID_321697245 A-to-I Human chr7 + 55772879 55772879 55772879 CATTTCTCCTCCGGGTGCTGTGGCTCATACCTATAATCCCAGCACCTTGGGAGGCCGAAGTGGGC CATTTCTCCTCCGGGTGCTGTGGCTCATACCTGTAATCCCAGCACCTTGGGAGGCCGAAGTGGGC A G PSPHP1 Ensembl:ENSG00000226278 Pseudogene intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1458422558 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18520586 52115 RMVar_ID_52115 Human_SNP_ID_321739881 A-to-I Human chr7 + 55941024 55941024 55941024 TGTATTTTTTAGTAGAGACACGGTTTCACCATATTGACTAGGCTGGTCTCGAACTCCTGACCTTG TGTATTTTTTAGTAGAGACACGGTTTCACCATGTTGACTAGGCTGGTCTCGAACTCCTGACCTTG A G AC092647.5,ZNF713 Ensembl:ENSG00000249773,Ensembl:ENSG00000178665 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1324655815 Functional Loss SNV dbSNP153 33..33 33 - - - 52116 RMVar_ID_52116 Human_SNP_ID_321739902 A-to-I Human chr7 + 55941103 55941103 55941103 CGGCCTCCCAAAGTGCTGGGATTATAGGCGTGAGCAACTGCACCTGGCAGGTTATGGTATAAAAC CGGCCTCCCAAAGTGCTGGGATTATAGGCGTGGGCAACTGCACCTGGCAGGTTATGGTATAAAAC A G AC092647.5,ZNF713 Ensembl:ENSG00000249773,Ensembl:ENSG00000178665 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1382627510 Functional Loss SNV dbSNP153 33..33 33 - - - 52117 RMVar_ID_52117 Human_SNP_ID_321739930 A-to-I Human chr7 + 55941206 55941206 55941206 GGCTGGGGGCGGTGGTTCACGCCTATAATCCCAGCACTTTGGGAGGCCGAGGTGGGGTGATCATC GGCTGGGGGCGGTGGTTCACGCCTATAATCCCCGCACTTTGGGAGGCCGAGGTGGGGTGATCATC A C AC092647.5,ZNF713 Ensembl:ENSG00000249773,Ensembl:ENSG00000178665 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs987221228 Functional Loss SNV dbSNP153 33..33 33 - - - 52118 RMVar_ID_52118 Human_SNP_ID_321739931 A-to-I Human chr7 + 55941206 55941206 55941206 GGCTGGGGGCGGTGGTTCACGCCTATAATCCCAGCACTTTGGGAGGCCGAGGTGGGGTGATCATC GGCTGGGGGCGGTGGTTCACGCCTATAATCCCGGCACTTTGGGAGGCCGAGGTGGGGTGATCATC A G AC092647.5,ZNF713 Ensembl:ENSG00000249773,Ensembl:ENSG00000178665 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs987221228 Functional Loss SNV dbSNP153 33..33 33 - - - 52119 RMVar_ID_52119 Human_SNP_ID_321739963 A-to-I Human chr7 + 55941335 55941335 55941335 AAAATTAGCTGGGTATGGTGGTGCACGCCTGTAGTCTCAGCAGCTTGGGAGGCTGAGGCAGAAGA AAAATTAGCTGGGTATGGTGGTGCACGCCTGTGGTCTCAGCAGCTTGGGAGGCTGAGGCAGAAGA A G AC092647.5,ZNF713 Ensembl:ENSG00000249773,Ensembl:ENSG00000178665 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1293217838 Functional Loss SNV dbSNP153 33..33 33 - - - 52120 RMVar_ID_52120 Human_SNP_ID_321739964 A-to-I Human chr7 + 55941335 55941335 55941335 AAAATTAGCTGGGTATGGTGGTGCACGCCTGTAGTCTCAGCAGCTTGGGAGGCTGAGGCAGAAGA AAAATTAGCTGGGTATGGTGGTGCACGCCTGTTGTCTCAGCAGCTTGGGAGGCTGAGGCAGAAGA A T AC092647.5,ZNF713 Ensembl:ENSG00000249773,Ensembl:ENSG00000178665 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1293217838 Functional Loss SNV dbSNP153 33..33 33 - - - 52121 RMVar_ID_52121 Human_SNP_ID_321740958 A-to-I Human chr7 + 55945421 55945421 55945421 TTTGATCAAAGCTTAATTTTGTGGCTGGGCGCAGTGGCTCATGCCTGTAATCCCAGCACTTTGGG TTTGATCAAAGCTTAATTTTGTGGCTGGGCGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGG A G AC092647.5 Ensembl:ENSG00000249773 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs918174392 Functional Loss SNV dbSNP153 33..33 33 - - - 52122 RMVar_ID_52122 Human_SNP_ID_321740983 A-to-I Human chr7 + 55945526 55945526 55945526 CAGCCTTGCCAATATGGTGAAACTCCGTCTCTACTAAAAATACAAAAATTAGCCGGGCATGGTGG CAGCCTTGCCAATATGGTGAAACTCCGTCTCTGCTAAAAATACAAAAATTAGCCGGGCATGGTGG A G AC092647.5 Ensembl:ENSG00000249773 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1355395553 Functional Loss SNV dbSNP153 33..33 33 - - - 52123 RMVar_ID_52123 Human_SNP_ID_321742990 A-to-I Human chr7 + 55952716 55952716 55952716 GAGATCGCGCCACTTCACTCCAGACTGGGCGAAAGAACTAAACTTCATCTAAAGAAAAATACATA GAGATCGCGCCACTTCACTCCAGACTGGGCGACAGAACTAAACTTCATCTAAAGAAAAATACATA A C AC092647.5,MRPS17,NIPSNAP2 Ensembl:ENSG00000249773,Ensembl:ENSG00000239789,Ensembl:ENSG00000146729 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1287535611 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8669110 52124 RMVar_ID_52124 Human_SNP_ID_321743838 A-to-I Human chr7 + 55955654 55955654 55955654 TATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGGTCTTGATCTCCTGACCTCGTGA TATTTTTAGTAGAGACGGGGTTTCACCGTGTTTGCCAGGATGGTCTTGATCTCCTGACCTCGTGA A T MRPS17,NIPSNAP2 Ensembl:ENSG00000239789,Ensembl:ENSG00000146729 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1214774845 Functional Loss SNV dbSNP153 33..33 33 - - - 52125 RMVar_ID_52125 Human_SNP_ID_321744003 A-to-I Human chr7 + 55956333 55956333 55956333 TAGGGATGGGGTTTCTCCATGTTTGTCAGGCTAGTCTTGAACTCCGGACCTCAGGTGATCCGCCC TAGGGATGGGGTTTCTCCATGTTTGTCAGGCTGGTCTTGAACTCCGGACCTCAGGTGATCCGCCC A G MRPS17,NIPSNAP2 Ensembl:ENSG00000239789,Ensembl:ENSG00000146729 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1136389 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16179333 52126 RMVar_ID_52126 Human_SNP_ID_321746430 A-to-I Human chr7 + 55965864 55965864 55965864 CGGCCTCCCAAAGTGCAGGGATTACAGTCGTGAATCACCAGGCGCGGCCTGATCTTTTTAAAAAG CGGCCTCCCAAAGTGCAGGGATTACAGTCGTGGATCACCAGGCGCGGCCTGATCTTTTTAAAAAG A G NIPSNAP2 Ensembl:ENSG00000146729 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1393603964 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123218,RMVar_hsa_circ_245197 52127 RMVar_ID_52127 Human_SNP_ID_321746577 A-to-I Human chr7 + 55966425 55966425 55966425 GCCCAGGAGTTTGAGACCAGCCTGGGCAACATAGTGGAACTCTGTCCCTAATAATAAATAAGTAC GCCCAGGAGTTTGAGACCAGCCTGGGCAACATGGTGGAACTCTGTCCCTAATAATAAATAAGTAC A G NIPSNAP2 Ensembl:ENSG00000146729 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs947012820 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16179366 RMVar_hsa_circ_123218,RMVar_hsa_circ_245197 52128 RMVar_ID_52128 Human_SNP_ID_321746653 A-to-I Human chr7 + 55966661 55966661 55966661 AAAATTAGCCCGGCATGGTGGCACACGCCTGTAGTCCCAGCTACTTGGTAGGCTGAGGTGGGAGT AAAATTAGCCCGGCATGGTGGCACACGCCTGTGGTCCCAGCTACTTGGTAGGCTGAGGTGGGAGT A G NIPSNAP2 Ensembl:ENSG00000146729 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1453444820 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123218,RMVar_hsa_circ_245197 52129 RMVar_ID_52129 Human_SNP_ID_321747152 A-to-I Human chr7 + 55968525 55968525 55968525 CTCCTGTCTCAGCCTCCCGATTAGCTGGGACTACAGGCGTGCGCCACCACAACCAGCTAATTTTT CTCCTGTCTCAGCCTCCCGATTAGCTGGGACTGCAGGCGTGCGCCACCACAACCAGCTAATTTTT A G NIPSNAP2 Ensembl:ENSG00000146729 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1394989320 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_123218,RMVar_hsa_circ_245197 52130 RMVar_ID_52130 Human_SNP_ID_321747263 A-to-I Human chr7 + 55968940 55968940 55968940 GTGGTGGTGCAGGGCTGTAGTCCCAGCTATACAGGTGGCTGAAGCAAGGTAATTGCTCGAGCGCA GTGGTGGTGCAGGGCTGTAGTCCCAGCTATACGGGTGGCTGAAGCAAGGTAATTGCTCGAGCGCA A G NIPSNAP2 Ensembl:ENSG00000146729 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs939779914 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17577398 RMVar_hsa_circ_123218,RMVar_hsa_circ_245197 52131 RMVar_ID_52131 Human_SNP_ID_321750739 A-to-I Human chr7 + 55981932 55981932 55981932 GGGTTTAAGCGATTCTTCTGCTTTAGCCTCCCAAGTAGCTGGAAATACAGGTGCCCACCACCACA GGGTTTAAGCGATTCTTCTGCTTTAGCCTCCCTAGTAGCTGGAAATACAGGTGCCCACCACCACA A T NIPSNAP2 Ensembl:ENSG00000146729 Protein coding intron GSE107867 ASD brains,frontal_cortex - 30559470 RNA-Seq:(High) rs1329785584 Functional Loss SNV dbSNP153 33..33 33 - - - 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_123151,RMVar_hsa_circ_245199,RMVar_hsa_circ_245198,RMVar_hsa_circ_113019,RMVar_hsa_circ_245204,RMVar_hsa_circ_101063,RMVar_hsa_circ_245201,RMVar_hsa_circ_245202,RMVar_hsa_circ_360934,RMVar_hsa_circ_371121,RMVar_hsa_circ_84434,RMVar_hsa_circ_245205,RMVar_hsa_circ_245203 52132 RMVar_ID_52132 Human_SNP_ID_321753273 A-to-I Human chr7 + 55990974 55990973 55990975 CACACCTGGCTAATATGTTTTGTATTTTTAGTAGAGACAGAGTTTCGCCATGTTGGCCAGGCTGA CACACCTGGCTAATATGTTTTGTATTTTTAGT__AGACAGAGTTTCGCCATGTTGGCCAGGCTGA TAG T NIPSNAP2 Ensembl:ENSG00000146729 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs894170597 Functional Loss DEL dbSNP153 33..34 33 - - - RMVar_hsa_circ_123218,RMVar_hsa_circ_362054,RMVar_hsa_circ_245197,RMVar_hsa_circ_245198,RMVar_hsa_circ_245209,RMVar_hsa_circ_245204,RMVar_hsa_circ_101063,RMVar_hsa_circ_84434,RMVar_hsa_circ_245205,RMVar_hsa_circ_290596,RMVar_hsa_circ_353182,RMVar_hsa_circ_275524,RMVar_hsa_circ_245208,RMVar_hsa_circ_309869,RMVar_hsa_circ_245210,RMVar_hsa_circ_337152 52133 RMVar_ID_52133 Human_SNP_ID_321758802 A-to-I Human chr7 - 56011523 56011523 56011523 TTTCCTGGAGAGGTTTTTTTTTTTTTTGAGACAGAATCTTGCTCTGTTGCCCAGGCTGGAGTGCA TTTCCTGGAGAGGTTTTTTTTTTTTTTGAGACTGAATCTTGCTCTGTTGCCCAGGCTGGAGTGCA T A PSPH Ensembl:ENSG00000146733 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1245333803 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_4945167,Human_RBP_ID_7746454 52134 RMVar_ID_52134 Human_SNP_ID_321762993 A-to-I Human chr7 - 56026437 56026437 56026437 TCACCCAGGCTGCAGTGCAGTGCAGTGGTGCAATCTCGGCTTACTGCAATCTCCATGTCTCCACC TCACCCAGGCTGCAGTGCAGTGCAGTGGTGCAGTCTCGGCTTACTGCAATCTCCATGTCTCCACC T C PSPH Ensembl:ENSG00000146733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1282719089 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_5270,RMVar_hsa_circ_24061 52135 RMVar_ID_52135 Human_SNP_ID_321765331 A-to-I Human chr7 - 56035106 56035106 56035106 GAACTCCTGACCTCAGGTGATCCGCTTGCCTCAGCCTCCCAAAGTGCTGGGATTACATGCTTGAG GAACTCCTGACCTCAGGTGATCCGCTTGCCTCTGCCTCCCAAAGTGCTGGGATTACATGCTTGAG T A PSPH Ensembl:ENSG00000146733 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1417394184 Functional Loss SNV dbSNP153 33..33 33 - - - 52136 RMVar_ID_52136 Human_SNP_ID_321765345 A-to-I Human chr7 - 56035149 56035149 56035149 TTTGCTGGAGATGGAGTTTTGCCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATC TTTGCTGGAGATGGAGTTTTGCCATGTTGGCCGGGCTGGTCTCGAACTCCTGACCTCAGGTGATC T C PSPH Ensembl:ENSG00000146733 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1205801967 Functional Loss SNV dbSNP153 33..33 33 - - - 52137 RMVar_ID_52137 Human_SNP_ID_321765350 A-to-I Human chr7 - 56035158 56035158 56035158 TTTTGTATTTTTGCTGGAGATGGAGTTTTGCCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCT TTTTGTATTTTTGCTGGAGATGGAGTTTTGCCGTGTTGGCCAGGCTGGTCTCGAACTCCTGACCT T C PSPH Ensembl:ENSG00000146733 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1435532422 Functional Loss SNV dbSNP153 33..33 33 - - - 52138 RMVar_ID_52138 Human_SNP_ID_321765354 A-to-I Human chr7 - 56035184 56035184 56035184 GGCATGCACCACCATGCCCCGCTAATTTTTGTATTTTTGCTGGAGATGGAGTTTTGCCATGTTGG GGCATGCACCACCATGCCCCGCTAATTTTTGTGTTTTTGCTGGAGATGGAGTTTTGCCATGTTGG T C PSPH Ensembl:ENSG00000146733 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1391575193 Functional Loss SNV dbSNP153 33..33 33 - - - 52139 RMVar_ID_52139 Human_SNP_ID_321765356 A-to-I Human chr7 - 56035192 56035192 56035192 GGACTACAGGCATGCACCACCATGCCCCGCTAATTTTTGTATTTTTGCTGGAGATGGAGTTTTGC GGACTACAGGCATGCACCACCATGCCCCGCTATTTTTTGTATTTTTGCTGGAGATGGAGTTTTGC T A PSPH Ensembl:ENSG00000146733 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs544513902 Functional Loss SNV dbSNP153 33..33 33 - - - 52140 RMVar_ID_52140 Human_SNP_ID_321765357 A-to-I Human chr7 - 56035192 56035192 56035192 GGACTACAGGCATGCACCACCATGCCCCGCTAATTTTTGTATTTTTGCTGGAGATGGAGTTTTGC GGACTACAGGCATGCACCACCATGCCCCGCTAGTTTTTGTATTTTTGCTGGAGATGGAGTTTTGC T C PSPH Ensembl:ENSG00000146733 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs544513902 Functional Loss SNV dbSNP153 33..33 33 - - - 52141 RMVar_ID_52141 Human_SNP_ID_321765372 A-to-I Human chr7 - 56035255 56035255 56035255 CTGCAACCTCCTCCCCCCACCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTACCAAGTAGCCGGG CTGCAACCTCCTCCCCCCACCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTACCAAGTAGCCGGG T C PSPH Ensembl:ENSG00000146733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs767536044 Functional Loss SNV dbSNP153 33..33 33 - - - 52142 RMVar_ID_52142 Human_SNP_ID_321765373 A-to-I Human chr7 - 56035255 56035255 56035255 CTGCAACCTCCTCCCCCCACCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTACCAAGTAGCCGGG CTGCAACCTCCTCCCCCCACCCGGGTTCAAGCCATTCTCCTGCCTCAGCCTACCAAGTAGCCGGG T G PSPH Ensembl:ENSG00000146733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs767536044 Functional Loss SNV dbSNP153 33..33 33 - - - 52143 RMVar_ID_52143 Human_SNP_ID_321765375 A-to-I Human chr7 - 56035258 56035258 56035258 TCACTGCAACCTCCTCCCCCCACCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTACCAAGTAGCC TCACTGCAACCTCCTCCCCCCACCCGGGTTCATGCAATTCTCCTGCCTCAGCCTACCAAGTAGCC T A PSPH Ensembl:ENSG00000146733 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs979094084 Functional Loss SNV dbSNP153 33..33 33 - - - 52144 RMVar_ID_52144 Human_SNP_ID_321765389 A-to-I Human chr7 - 56035298 56035298 56035298 CTCTGTTGCTCAGGCTGTAGTGCAGTGGCACGATCTTGGTTCACTGCAACCTCCTCCCCCCACCC CTCTGTTGCTCAGGCTGTAGTGCAGTGGCACGGTCTTGGTTCACTGCAACCTCCTCCCCCCACCC T C PSPH Ensembl:ENSG00000146733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs560324599 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17578085 52145 RMVar_ID_52145 Human_SNP_ID_321765390 A-to-I Human chr7 - 56035307 56035307 56035307 GGAGTTTCACTCTGTTGCTCAGGCTGTAGTGCAGTGGCACGATCTTGGTTCACTGCAACCTCCTC GGAGTTTCACTCTGTTGCTCAGGCTGTAGTGCCGTGGCACGATCTTGGTTCACTGCAACCTCCTC T G PSPH Ensembl:ENSG00000146733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs527380758 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_17578085 52146 RMVar_ID_52146 Human_SNP_ID_321765624 A-to-I Human chr7 - 56036507 56036507 56036507 CTCCCGCCTCAGCCTCCCAAGTAGCTGGGACTATAGGCATGCACCACCACACCCAGCCAGATTTT CTCCCGCCTCAGCCTCCCAAGTAGCTGGGACTGTAGGCATGCACCACCACACCCAGCCAGATTTT T C PSPH Ensembl:ENSG00000146733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1415873090 Functional Loss SNV dbSNP153 33..33 33 - - - 52147 RMVar_ID_52147 Human_SNP_ID_321765632 A-to-I Human chr7 - 56036545 56036545 56036545 GGCTCACTGTAACCTCGAAATCCTGGGCTCAAATGATCCTCCCGCCTCAGCCTCCCAAGTAGCTG GGCTCACTGTAACCTCGAAATCCTGGGCTCAAGTGATCCTCCCGCCTCAGCCTCCCAAGTAGCTG T C PSPH Ensembl:ENSG00000146733 Protein coding intron GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs1229661091 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8669145 52148 RMVar_ID_52148 Human_SNP_ID_321765633 A-to-I Human chr7 - 56036546 56036546 56036546 CGGCTCACTGTAACCTCGAAATCCTGGGCTCAAATGATCCTCCCGCCTCAGCCTCCCAAGTAGCT CGGCTCACTGTAACCTCGAAATCCTGGGCTCAGATGATCCTCCCGCCTCAGCCTCCCAAGTAGCT T C PSPH Ensembl:ENSG00000146733 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1284372771 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8669145 52149 RMVar_ID_52149 Human_SNP_ID_321765639 A-to-I Human chr7 - 56036567 56036567 56036567 TGGAGTACAGTGGCATGATCACGGCTCACTGTAACCTCGAAATCCTGGGCTCAAATGATCCTCCC TGGAGTACAGTGGCATGATCACGGCTCACTGTTACCTCGAAATCCTGGGCTCAAATGATCCTCCC T A PSPH Ensembl:ENSG00000146733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1236083795 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_8669145,Human_RBP_ID_16179977,Human_RBP_ID_26107683 52150 RMVar_ID_52150 Human_SNP_ID_321765644 A-to-I Human chr7 - 56036585 56036585 56036585 TTGCTCTGTTACCCAGACTGGAGTACAGTGGCATGATCACGGCTCACTGTAACCTCGAAATCCTG TTGCTCTGTTACCCAGACTGGAGTACAGTGGCTTGATCACGGCTCACTGTAACCTCGAAATCCTG T A PSPH Ensembl:ENSG00000146733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs890154897 Functional Loss SNV dbSNP153 33..33 33 - - - 52151 RMVar_ID_52151 Human_SNP_ID_321765645 A-to-I Human chr7 - 56036585 56036585 56036585 TTGCTCTGTTACCCAGACTGGAGTACAGTGGCATGATCACGGCTCACTGTAACCTCGAAATCCTG TTGCTCTGTTACCCAGACTGGAGTACAGTGGCGTGATCACGGCTCACTGTAACCTCGAAATCCTG T C PSPH Ensembl:ENSG00000146733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs890154897 Functional Loss SNV dbSNP153 33..33 33 - - - 52152 RMVar_ID_52152 Human_SNP_ID_321765648 A-to-I Human chr7 - 56036593 56036593 56036593 ACAAGGGCTTGCTCTGTTACCCAGACTGGAGTACAGTGGCATGATCACGGCTCACTGTAACCTCG ACAAGGGCTTGCTCTGTTACCCAGACTGGAGTGCAGTGGCATGATCACGGCTCACTGTAACCTCG T C PSPH Ensembl:ENSG00000146733 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1455273770 Functional Loss SNV dbSNP153 33..33 33 - - - 52153 RMVar_ID_52153 Human_SNP_ID_321765658 A-to-I Human chr7 - 56036622 56036622 56036622 TAATTAATTAACTAATTAATTTTTCAGAGACAAGGGCTTGCTCTGTTACCCAGACTGGAGTACAG TAATTAATTAACTAATTAATTTTTCAGAGACAGGGGCTTGCTCTGTTACCCAGACTGGAGTACAG T C PSPH Ensembl:ENSG00000146733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1186930699 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3095216,Human_RBP_ID_16179979 52154 RMVar_ID_52154 Human_SNP_ID_321765857 A-to-I Human chr7 - 56037547 56037547 56037547 TGGTGTGGTGGCACACACCTGTGGTCCAACCTACTCGGAAGGCTGAGGCAGGAAGATTGCTTGAG TGGTGTGGTGGCACACACCTGTGGTCCAACCTGCTCGGAAGGCTGAGGCAGGAAGATTGCTTGAG T C PSPH Ensembl:ENSG00000146733 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1406225840 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16180004 52155 RMVar_ID_52155 Human_SNP_ID_321766255 A-to-I Human chr7 - 56039015 56039015 56039015 CCTTGGCCTCCTGAGTAACTAGGATTACAGGTATGCACCACTACACCCAGCTAATTTTGTATTTT CCTTGGCCTCCTGAGTAACTAGGATTACAGGTGTGCACCACTACACCCAGCTAATTTTGTATTTT T C PSPH Ensembl:ENSG00000146733 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1370799371 Functional Loss SNV dbSNP153 33..33 33 - - - 52156 RMVar_ID_52156 Human_SNP_ID_321766415 A-to-I Human chr7 - 56039610 56039610 56039610 TACCATGCCCAGCTAATTTTTTGTATTTTAGTAGAGATGGGCTTTCACCATGTTGGCCAGGATGG TACCATGCCCAGCTAATTTTTTGTATTTTAGTGGAGATGGGCTTTCACCATGTTGGCCAGGATGG T C PSPH Ensembl:ENSG00000146733 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1303109597 Functional Loss SNV dbSNP153 33..33 33 - - - 52157 RMVar_ID_52157 Human_SNP_ID_321766433 A-to-I Human chr7 - 56039707 56039707 56039707 CAGTGGTGCAATCTCGGCTTACTGCAACCTCCACTTCCTGGGTTCAAGCGATTTCCCTGCTTCAG CAGTGGTGCAATCTCGGCTTACTGCAACCTCCCCTTCCTGGGTTCAAGCGATTTCCCTGCTTCAG T G PSPH Ensembl:ENSG00000146733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs549054987 Functional Loss SNV dbSNP153 33..33 33 - - - 52158 RMVar_ID_52158 Human_SNP_ID_321766439 A-to-I Human chr7 - 56039729 56039729 56039729 TCTCTGTCACCAGGGTGGAGTGCAGTGGTGCAATCTCGGCTTACTGCAACCTCCACTTCCTGGGT TCTCTGTCACCAGGGTGGAGTGCAGTGGTGCAGTCTCGGCTTACTGCAACCTCCACTTCCTGGGT T C PSPH Ensembl:ENSG00000146733 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1284184215 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_3125140,Human_RBP_ID_16180033 52159 RMVar_ID_52159 Human_SNP_ID_321766697 A-to-I Human chr7 - 56040456 56040456 56040456 CCAGAAGGCAGAGATTGTAGTGTGTTGAGATTACACCACGGAACTCCAGCCTGGACAGAGACAGA CCAGAAGGCAGAGATTGTAGTGTGTTGAGATTGCACCACGGAACTCCAGCCTGGACAGAGACAGA T C PSPH Ensembl:ENSG00000146733 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs11549718 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16180047,Human_RBP_ID_23315769 52160 RMVar_ID_52160 Human_SNP_ID_321766865 A-to-I Human chr7 - 56041192 56041189 56041193 AAAAAAAAAAAAAAAGAGAGAGAGAGAGAGATAGAGTCTTGCTATGATAATCAAGCTGGTCTTGC AAAAAAAAAAAAAAAGAGAGAGAGAGAGAGA____GTCTTGCTATGATAATCAAGCTGGTCTTGC CTCTA C PSPH Ensembl:ENSG00000146733 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs899877327 Functional Loss DEL dbSNP153 32..35 33 - - - 52161 RMVar_ID_52161 Human_SNP_ID_321766938 A-to-I Human chr7 - 56041328 56041328 56041328 GGCACCTGTGGTCCCAGCTATTTGGGAGGCTGAGGCAGAAGAATCGCTTGAACCTGGGAGGCAGA GGCACCTGTGGTCCCAGCTATTTGGGAGGCTGCGGCAGAAGAATCGCTTGAACCTGGGAGGCAGA T G PSPH Ensembl:ENSG00000146733 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1249302415 Functional Loss SNV dbSNP153 33..33 33 - - - 52162 RMVar_ID_52162 Human_SNP_ID_321766957 A-to-I Human chr7 - 56041401 56041401 56041401 CGAGACCATCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCTGGGCA CGAGACCATCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTAGCTGGGCA T C PSPH Ensembl:ENSG00000146733 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs56274706 Functional Loss SNV dbSNP153 33..33 33 - - - 52163 RMVar_ID_52163 Human_SNP_ID_321766960 A-to-I Human chr7 - 56041406 56041406 56041406 GAGATCGAGACCATCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCT GAGATCGAGACCATCCTGGCCAACATGGTGAAGCCCCATCTCTACTAAAAATACAAAAATTAGCT T C PSPH Ensembl:ENSG00000146733 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1484380501 Functional Loss SNV dbSNP153 33..33 33 - - - 52164 RMVar_ID_52164 Human_SNP_ID_321767062 A-to-I Human chr7 - 56041876 56041876 56041876 TCTGTTGCCCAGGCTAGAGTGCCAGTGGCACAATCTCAGCTGACTGCAACCTCTGCCTCCCAGTT TCTGTTGCCCAGGCTAGAGTGCCAGTGGCACATTCTCAGCTGACTGCAACCTCTGCCTCCCAGTT T A PSPH Ensembl:ENSG00000146733 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1174372412 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16180098 RMVar_hsa_circ_245219,RMVar_hsa_circ_92708,RMVar_hsa_circ_102241,RMVar_hsa_circ_245220 52165 RMVar_ID_52165 Human_SNP_ID_321767063 A-to-I Human chr7 - 56041876 56041876 56041876 TCTGTTGCCCAGGCTAGAGTGCCAGTGGCACAATCTCAGCTGACTGCAACCTCTGCCTCCCAGTT TCTGTTGCCCAGGCTAGAGTGCCAGTGGCACAGTCTCAGCTGACTGCAACCTCTGCCTCCCAGTT T C PSPH Ensembl:ENSG00000146733 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line - 29129909,31158229 RNA-Seq:(High) rs1174372412 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16180098 RMVar_hsa_circ_245219,RMVar_hsa_circ_92708,RMVar_hsa_circ_102241,RMVar_hsa_circ_245220 52166 RMVar_ID_52166 Human_SNP_ID_321767127 A-to-I Human chr7 - 56042053 56042053 56042053 ACACCCTGGTAATTTTTGTAGTTTTAGTAGAGACGAGGTTTCACCCTGTTGGCCAGGCTGGTCTC ACACCCTGGTAATTTTTGTAGTTTTAGTAGAGGCGAGGTTTCACCCTGTTGGCCAGGCTGGTCTC T C PSPH Ensembl:ENSG00000146733 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1324956986 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16289523 RMVar_hsa_circ_92708,RMVar_hsa_circ_245220 52167 RMVar_ID_52167 Human_SNP_ID_321767129 A-to-I Human chr7 - 56042060 56042060 56042060 CGACACCACACCCTGGTAATTTTTGTAGTTTTAGTAGAGACGAGGTTTCACCCTGTTGGCCAGGC CGACACCACACCCTGGTAATTTTTGTAGTTTTCGTAGAGACGAGGTTTCACCCTGTTGGCCAGGC T G PSPH Ensembl:ENSG00000146733 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1218059582 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16289523 RMVar_hsa_circ_92708,RMVar_hsa_circ_245220 52168 RMVar_ID_52168 Human_SNP_ID_321767142 A-to-I Human chr7 - 56042114 56042114 56042114 GATTCAAGCGATTCTCCTGCTTCAGCCTCCCAAGTAGCTGGGATTACAGGTGCACGACACCACAC GATTCAAGCGATTCTCCTGCTTCAGCCTCCCAGGTAGCTGGGATTACAGGTGCACGACACCACAC T C PSPH Ensembl:ENSG00000146733 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs544550789 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92708,RMVar_hsa_circ_245220 52169 RMVar_ID_52169 Human_SNP_ID_321767171 A-to-I Human chr7 - 56042210 56042210 56042210 ACAGATTTTTTTTTTTTTTTTTTTGAGACAGAATCTCGCTCTGTCGCCCAGGCTGGAGTGTAGGG ACAGATTTTTTTTTTTTTTTTTTTGAGACAGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGTAGGG T C PSPH Ensembl:ENSG00000146733 Protein coding intron GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line - 23474544,24183664,29129909 RNA-Seq:(High) rs1353184456 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92708,RMVar_hsa_circ_245220 52170 RMVar_ID_52170 Human_SNP_ID_321767173 A-to-I Human chr7 - 56042215 56042215 56042215 TTCAGACAGATTTTTTTTTTTTTTTTTTTGAGACAGAATCTCGCTCTGTCGCCCAGGCTGGAGTG TTCAGACAGATTTTTTTTTTTTTTTTTTTGAGGCAGAATCTCGCTCTGTCGCCCAGGCTGGAGTG T C PSPH Ensembl:ENSG00000146733 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1450682248 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_92708,RMVar_hsa_circ_245220 52171 RMVar_ID_52171 Human_SNP_ID_321767174 A-to-I Human chr7 - 56042217 56042216 56042217 TTTTCAGACAGATTTTTTTTTTTTTTTTTTTGAGACAGAATCTCGCTCTGTCGCCCAGGCTGGAG TTTTCAGACAGATTTTTTTTTTTTTTTTTTTG_GACAGAATCTCGCTCTGTCGCCCAGGCTGGAG CT C PSPH Ensembl:ENSG00000146733 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1394515726 Functional Loss DEL dbSNP153 33..33 33 - - - RMVar_hsa_circ_92708,RMVar_hsa_circ_245220 52172 RMVar_ID_52172 Human_SNP_ID_321767236 A-to-I Human chr7 - 56042479 56042479 56042479 ACCTGGATAATTTTTTGATGTTTTGTAGAGACAGTGCTTCAGTTTGTTGCCTGTGCTGGTCTTGA ACCTGGATAATTTTTTGATGTTTTGTAGAGACCGTGCTTCAGTTTGTTGCCTGTGCTGGTCTTGA T G PSPH Ensembl:ENSG00000146733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1160338863 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_686139,Human_RBP_ID_1221817,Human_RBP_ID_2044349,Human_RBP_ID_7746544,Human_RBP_ID_16180103 Human_miRNA_ID_2733431,Human_miRNA_ID_2904595 RMVar_hsa_circ_92708,RMVar_hsa_circ_245220,RMVar_hsa_circ_125152,RMVar_hsa_circ_245221 52173 RMVar_ID_52173 Human_SNP_ID_321767242 A-to-I Human chr7 - 56042526 56042526 56042526 CTGCCTCAGCCTCCTGTGTAGCTGGGACCACAAGCACTCGTCACCACACCTGGATAATTTTTTGA CTGCCTCAGCCTCCTGTGTAGCTGGGACCACAGGCACTCGTCACCACACCTGGATAATTTTTTGA T C PSPH Ensembl:ENSG00000146733 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1269622436 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16180103 RMVar_hsa_circ_92708,RMVar_hsa_circ_245220,RMVar_hsa_circ_125152,RMVar_hsa_circ_245221 52174 RMVar_ID_52174 Human_SNP_ID_321767404 A-to-I Human chr7 - 56043186 56043186 56043186 CAGCTCACTGCAACCTCCCCTTCCCAAGTTCAAGCAATTTTCATGCCGCAGCCTCCTAGCTGGGA CAGCTCACTGCAACCTCCCCTTCCCAAGTTCAGGCAATTTTCATGCCGCAGCCTCCTAGCTGGGA T C PSPH Ensembl:ENSG00000146733 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs953157391 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_868932,Human_Splice_Rec_868933 RMVar_hsa_circ_125152,RMVar_hsa_circ_245221 52175 RMVar_ID_52175 Human_SNP_ID_321767407 A-to-I Human chr7 - 56043193 56043193 56043193 GCCATCTCAGCTCACTGCAACCTCCCCTTCCCAAGTTCAAGCAATTTTCATGCCGCAGCCTCCTA GCCATCTCAGCTCACTGCAACCTCCCCTTCCCCAGTTCAAGCAATTTTCATGCCGCAGCCTCCTA T G PSPH Ensembl:ENSG00000146733 Protein coding intron GSE47997 K562 cells&HepG2 cells - 23474544 RNA-Seq:(High) rs1229976386 Functional Loss SNV dbSNP153 33..33 33 - - - Human_Splice_Rec_868932,Human_Splice_Rec_868933 RMVar_hsa_circ_125152,RMVar_hsa_circ_245221 52176 RMVar_ID_52176 Human_SNP_ID_321767654 A-to-I Human chr7 - 56044085 56044085 56044085 ATACAAAATTAGCCAGGCGTGTATTCCCAGCTACACGGGAGGCTGAGGCAGGAGAATCACTTGAA ATACAAAATTAGCCAGGCGTGTATTCCCAGCTGCACGGGAGGCTGAGGCAGGAGAATCACTTGAA T C PSPH Ensembl:ENSG00000146733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1248911467 Functional Loss SNV dbSNP153 33..33 33 - - - 52177 RMVar_ID_52177 Human_SNP_ID_321767976 A-to-I Human chr7 - 56045457 56045454 56045458 TTAATTTTTTCTTTTATATATTTTTAAGAGATAGAGTCTCACTCTGGTGCCCAGGCTGGAGTGCA TTAATTTTTTCTTTTATATATTTTTAAGAGA____GTCTCACTCTGGTGCCCAGGCTGGAGTGCA CTCTA C PSPH Ensembl:ENSG00000146733 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1201678333 Functional Loss DEL dbSNP153 32..35 33 - - - Human_RBP_ID_7746563,Human_RBP_ID_16180149,Human_RBP_ID_22483497 52178 RMVar_ID_52178 Human_SNP_ID_321768206 A-to-I Human chr7 - 56046439 56046439 56046439 ATCCTTTGAGGCCAGGAGTTCAAGACCAGCCTAGACAACATGGTGAGACCCCATCTCTACAAAAA ATCCTTTGAGGCCAGGAGTTCAAGACCAGCCTTGACAACATGGTGAGACCCCATCTCTACAAAAA T A PSPH Ensembl:ENSG00000146733 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1316374709 Functional Loss SNV dbSNP153 33..33 33 - - - 52179 RMVar_ID_52179 Human_SNP_ID_321768404 A-to-I Human chr7 - 56047270 56047270 56047270 TTCCTATCTCAGCCTCCTGAGTAGCTGAGACTACAGACGTGCACCACTATGGCTGGCTAATTTAA TTCCTATCTCAGCCTCCTGAGTAGCTGAGACTGCAGACGTGCACCACTATGGCTGGCTAATTTAA T C PSPH Ensembl:ENSG00000146733 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1217654256 Functional Loss SNV dbSNP153 33..33 33 - - - 52180 RMVar_ID_52180 Human_SNP_ID_321768405 A-to-I Human chr7 - 56047275 56047275 56047275 TCAGCTTCCTATCTCAGCCTCCTGAGTAGCTGAGACTACAGACGTGCACCACTATGGCTGGCTAA TCAGCTTCCTATCTCAGCCTCCTGAGTAGCTGCGACTACAGACGTGCACCACTATGGCTGGCTAA T G PSPH Ensembl:ENSG00000146733 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1033338394 Functional Loss SNV dbSNP153 33..33 33 - - - 52181 RMVar_ID_52181 Human_SNP_ID_321768416 A-to-I Human chr7 - 56047325 56047325 56047325 GAGTGCAGTAGCTCAATCACACAGCTTACTGCAGCCTGAACCTCCTGGGCTCAGCTTCCTATCTC GAGTGCAGTAGCTCAATCACACAGCTTACTGCGGCCTGAACCTCCTGGGCTCAGCTTCCTATCTC T C PSPH Ensembl:ENSG00000146733 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1382440000 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16180173 52182 RMVar_ID_52182 Human_SNP_ID_321768546 A-to-I Human chr7 - 56047871 56047871 56047871 GTGAGGTCAAGAGATCAAGACCATCCTGGCCAACATGGTGCAACACCGTCTCTACTAAAAATACA GTGAGGTCAAGAGATCAAGACCATCCTGGCCACCATGGTGCAACACCGTCTCTACTAAAAATACA T G PSPH Ensembl:ENSG00000146733 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1362895243 Functional Loss SNV dbSNP153 33..33 33 - - - 52183 RMVar_ID_52183 Human_SNP_ID_321768749 A-to-I Human chr7 - 56048731 56048731 56048731 GCTACTTGTGTGGCTGAGGTGGAATTGCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCCAGAAT GCTACTTGTGTGGCTGAGGTGGAATTGCTTGAGCCCAGGAGGCGGAGGTTGCAGTGAGCCAGAAT T C PSPH Ensembl:ENSG00000146733 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1392273270 Functional Loss SNV dbSNP153 33..33 33 - - - 52184 RMVar_ID_52184 Human_SNP_ID_321768996 A-to-I Human chr7 - 56049537 56049537 56049537 TTCCTCGGGAGGCTGAGGCGGGAGAATCACTTAAACCTGGGAGTTGGAGATTGCAGTGAGCGGAG TTCCTCGGGAGGCTGAGGCGGGAGAATCACTTGAACCTGGGAGTTGGAGATTGCAGTGAGCGGAG T C PSPH Ensembl:ENSG00000146733 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1271175227 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16180214,Human_RBP_ID_26107758 52185 RMVar_ID_52185 Human_SNP_ID_321769201 A-to-I Human chr7 - 56050334 56050334 56050334 TGGAATCTGGGAGGTGGAGGTTGCAGTCAGCTATGATCTTGCCACTGCACTTCAGCCTGGGCTAC TGGAATCTGGGAGGTGGAGGTTGCAGTCAGCTGTGATCTTGCCACTGCACTTCAGCCTGGGCTAC T C PSPH Ensembl:ENSG00000146733 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1312024449 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_26138285 52186 RMVar_ID_52186 Human_SNP_ID_321769308 A-to-I Human chr7 - 56050768 56050768 56050768 AACACTAGAGACAAGCAAAGTTACCCCTGGGTACTCTATGAATTTTCGGAATGCTTTCTGAATTT AACACTAGAGACAAGCAAAGTTACCCCTGGGTTCTCTATGAATTTTCGGAATGCTTTCTGAATTT T A PSPH Ensembl:ENSG00000146733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1056721078 Functional Loss SNV dbSNP153 33..33 33 - - - 52187 RMVar_ID_52187 Human_SNP_ID_321769309 A-to-I Human chr7 - 56050768 56050768 56050768 AACACTAGAGACAAGCAAAGTTACCCCTGGGTACTCTATGAATTTTCGGAATGCTTTCTGAATTT AACACTAGAGACAAGCAAAGTTACCCCTGGGTGCTCTATGAATTTTCGGAATGCTTTCTGAATTT T C PSPH Ensembl:ENSG00000146733 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1056721078 Functional Loss SNV dbSNP153 33..33 33 - - - 52188 RMVar_ID_52188 Human_SNP_ID_321769382 A-to-I Human chr7 - 56051015 56051015 56051015 TTATTTTCTTTTTGTAAACATAGGGTCTCACTATGTTGCCCAGGGTGGTCTCAAACTCCTGAGCT TTATTTTCTTTTTGTAAACATAGGGTCTCACTGTGTTGCCCAGGGTGGTCTCAAACTCCTGAGCT T C PSPH Ensembl:ENSG00000146733 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs561900056 Functional Loss SNV dbSNP153 33..33 33 - - - 52189 RMVar_ID_52189 Human_SNP_ID_321770094 A-to-I Human chr7 + 56052863 56052863 56052863 TCGACCAGCCTGGAGTCCGGTGGCACAATCTCAACTCACTGCAACCTCTCCCTCCCGGGTTCAAG TCGACCAGCCTGGAGTCCGGTGGCACAATCTCGACTCACTGCAACCTCTCCCTCCCGGGTTCAAG A G CCT6A Ensembl:ENSG00000146731 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line - 31158229 RNA-Seq:(High) rs761415724 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_16180292 RMVar_hsa_circ_56964,RMVar_hsa_circ_370903,RMVar_hsa_circ_102641,RMVar_hsa_circ_245222,RMVar_hsa_circ_374501,RMVar_hsa_circ_322748,RMVar_hsa_circ_348074,RMVar_hsa_circ_66102,RMVar_hsa_circ_245223,RMVar_hsa_circ_245225,RMVar_hsa_circ_54936,RMVar_hsa_circ_245224 52190 RMVar_ID_52190 Human_SNP_ID_321770121 A-to-I Human chr7 + 56052955 56052955 56052955 AGCTAGGATTACAGGCTCGCGCCACTACGCCCAGTTGATTTTTGTATTTTTAGTAGAGACAGGAT AGCTAGGATTACAGGCTCGCGCCACTACGCCCCGTTGATTTTTGTATTTTTAGTAGAGACAGGAT A C CCT6A Ensembl:ENSG00000146731 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs929522595 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56964,RMVar_hsa_circ_370903,RMVar_hsa_circ_102641,RMVar_hsa_circ_245222,RMVar_hsa_circ_374501,RMVar_hsa_circ_322748,RMVar_hsa_circ_348074,RMVar_hsa_circ_66102,RMVar_hsa_circ_245223,RMVar_hsa_circ_245225,RMVar_hsa_circ_54936,RMVar_hsa_circ_245224 52191 RMVar_ID_52191 Human_SNP_ID_321770122 A-to-I Human chr7 + 56052955 56052955 56052955 AGCTAGGATTACAGGCTCGCGCCACTACGCCCAGTTGATTTTTGTATTTTTAGTAGAGACAGGAT AGCTAGGATTACAGGCTCGCGCCACTACGCCCGGTTGATTTTTGTATTTTTAGTAGAGACAGGAT A G CCT6A Ensembl:ENSG00000146731 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line - 29129909,31158229,31158229 RNA-Seq:(High) rs929522595 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56964,RMVar_hsa_circ_370903,RMVar_hsa_circ_102641,RMVar_hsa_circ_245222,RMVar_hsa_circ_374501,RMVar_hsa_circ_322748,RMVar_hsa_circ_348074,RMVar_hsa_circ_66102,RMVar_hsa_circ_245223,RMVar_hsa_circ_245225,RMVar_hsa_circ_54936,RMVar_hsa_circ_245224 52192 RMVar_ID_52192 Human_SNP_ID_321770286 A-to-I Human chr7 + 56053625 56053625 56053625 AAAATACAAAAATTAGCCGGGTGTGGTCCTGCACGCCTGTAGTCCCAGCTGCTTCAGAGGCTGAG AAAATACAAAAATTAGCCGGGTGTGGTCCTGCGCGCCTGTAGTCCCAGCTGCTTCAGAGGCTGAG A G CCT6A Ensembl:ENSG00000146731 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1218903097 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_56964,RMVar_hsa_circ_370903,RMVar_hsa_circ_102641,RMVar_hsa_circ_245222,RMVar_hsa_circ_374501,RMVar_hsa_circ_322748,RMVar_hsa_circ_348074,RMVar_hsa_circ_66102,RMVar_hsa_circ_245223,RMVar_hsa_circ_245225,RMVar_hsa_circ_54936,RMVar_hsa_circ_245224 52193 RMVar_ID_52193 Human_SNP_ID_321771111 A-to-I Human chr7 + 56056461 56056461 56056461 ACTGTGAAATACTAATGGGCATGGAGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGTGGT ACTGTGAAATACTAATGGGCATGGAGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGTGGT A G CCT6A Ensembl:ENSG00000146731 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs761870846 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_18102202,Human_RBP_ID_19134918 RMVar_hsa_circ_27556,RMVar_hsa_circ_370903,RMVar_hsa_circ_102641,RMVar_hsa_circ_245222,RMVar_hsa_circ_374501,RMVar_hsa_circ_348074,RMVar_hsa_circ_245225,RMVar_hsa_circ_54936,RMVar_hsa_circ_245224,RMVar_hsa_circ_297064,RMVar_hsa_circ_339420,RMVar_hsa_circ_54517,RMVar_hsa_circ_65647,RMVar_hsa_circ_245226,RMVar_hsa_circ_319023,RMVar_hsa_circ_337053,RMVar_hsa_circ_315704,RMVar_hsa_circ_117216,RMVar_hsa_circ_57889 52194 RMVar_ID_52194 Human_SNP_ID_321771124 A-to-I Human chr7 + 56056536 56056536 56056536 CCTCAGGTCAGGAGTTCCAGACCAGCCTGGCCAACATGGGGAAACCCCGTCTCTATTAAAATTAC CCTCAGGTCAGGAGTTCCAGACCAGCCTGGCCGACATGGGGAAACCCCGTCTCTATTAAAATTAC A G CCT6A Ensembl:ENSG00000146731 Protein coding intron GSE38233 cultured B-cells - 24183664 RNA-Seq:(High) rs1256968706 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27556,RMVar_hsa_circ_370903,RMVar_hsa_circ_102641,RMVar_hsa_circ_245222,RMVar_hsa_circ_374501,RMVar_hsa_circ_348074,RMVar_hsa_circ_245225,RMVar_hsa_circ_54936,RMVar_hsa_circ_245224,RMVar_hsa_circ_297064,RMVar_hsa_circ_339420,RMVar_hsa_circ_54517,RMVar_hsa_circ_65647,RMVar_hsa_circ_245226,RMVar_hsa_circ_319023,RMVar_hsa_circ_337053,RMVar_hsa_circ_315704,RMVar_hsa_circ_117216,RMVar_hsa_circ_57889 52195 RMVar_ID_52195 Human_SNP_ID_321771243 A-to-I Human chr7 + 56056858 56056858 56056858 GCTCTGTCGCCCAGCCTGGAGTGTACAGTGGCATGATCTCGGCTCACTGCAAGCTCTGCCTCCCG GCTCTGTCGCCCAGCCTGGAGTGTACAGTGGCGTGATCTCGGCTCACTGCAAGCTCTGCCTCCCG A G CCT6A Ensembl:ENSG00000146731 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1490552241 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27556,RMVar_hsa_circ_370903,RMVar_hsa_circ_102641,RMVar_hsa_circ_245222,RMVar_hsa_circ_374501,RMVar_hsa_circ_348074,RMVar_hsa_circ_245225,RMVar_hsa_circ_54936,RMVar_hsa_circ_245224,RMVar_hsa_circ_297064,RMVar_hsa_circ_339420,RMVar_hsa_circ_54517,RMVar_hsa_circ_65647,RMVar_hsa_circ_245226,RMVar_hsa_circ_319023,RMVar_hsa_circ_337053,RMVar_hsa_circ_315704,RMVar_hsa_circ_117216,RMVar_hsa_circ_57889 52196 RMVar_ID_52196 Human_SNP_ID_321771246 A-to-I Human chr7 + 56056861 56056861 56056861 CTGTCGCCCAGCCTGGAGTGTACAGTGGCATGATCTCGGCTCACTGCAAGCTCTGCCTCCCGGGT CTGTCGCCCAGCCTGGAGTGTACAGTGGCATGGTCTCGGCTCACTGCAAGCTCTGCCTCCCGGGT A G CCT6A Ensembl:ENSG00000146731 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1339760705 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_27556,RMVar_hsa_circ_370903,RMVar_hsa_circ_102641,RMVar_hsa_circ_245222,RMVar_hsa_circ_374501,RMVar_hsa_circ_348074,RMVar_hsa_circ_245225,RMVar_hsa_circ_54936,RMVar_hsa_circ_245224,RMVar_hsa_circ_297064,RMVar_hsa_circ_339420,RMVar_hsa_circ_54517,RMVar_hsa_circ_65647,RMVar_hsa_circ_245226,RMVar_hsa_circ_319023,RMVar_hsa_circ_337053,RMVar_hsa_circ_315704,RMVar_hsa_circ_117216,RMVar_hsa_circ_57889 52197 RMVar_ID_52197 Human_SNP_ID_321775711 A-to-I Human chr7 + 56072065 56072065 56072065 AGGAGGTGGAGGTTGCAGTGAGCTGAGATTGCACCACTGCACTCCAGCCTGGGCAACAGTCTTTT AGGAGGTGGAGGTTGCAGTGAGCTGAGATTGCGCCACTGCACTCCAGCCTGGGCAACAGTCTTTT A G SUMF2 Ensembl:ENSG00000129103 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1297240725 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_22011830 RMVar_hsa_circ_65684,RMVar_hsa_circ_95157,RMVar_hsa_circ_245233,RMVar_hsa_circ_272731,RMVar_hsa_circ_245234 52198 RMVar_ID_52198 Human_SNP_ID_321776564 A-to-I Human chr7 + 56074916 56074916 56074916 GGCCAGGAGTAAAAGACTAGCCTGGGCAATATAGGGAGACCCTGTCTCTCCGAAAAATACAAAAA GGCCAGGAGTAAAAGACTAGCCTGGGCAATATTGGGAGACCCTGTCTCTCCGAAAAATACAAAAA A T SUMF2 Ensembl:ENSG00000129103 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1233267339 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95157,RMVar_hsa_circ_245233,RMVar_hsa_circ_107831,RMVar_hsa_circ_120881,RMVar_hsa_circ_365756,RMVar_hsa_circ_245235,RMVar_hsa_circ_245237,RMVar_hsa_circ_90943,RMVar_hsa_circ_245236,RMVar_hsa_circ_245239,RMVar_hsa_circ_100762,RMVar_hsa_circ_245238 52199 RMVar_ID_52199 Human_SNP_ID_321776778 A-to-I Human chr7 + 56075892 56075892 56075892 TTTGTTTTTTGTTTTTTGTTTTGAGACAGTCTAGCTCTGTCGCCCAAGGCTGGAGTACAGTGGCA TTTGTTTTTTGTTTTTTGTTTTGAGACAGTCTGGCTCTGTCGCCCAAGGCTGGAGTACAGTGGCA A G SUMF2 Ensembl:ENSG00000129103 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line - 24183664,29129909 RNA-Seq:(High) rs1478203918 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_23315464 RMVar_hsa_circ_95157,RMVar_hsa_circ_245233,RMVar_hsa_circ_107831,RMVar_hsa_circ_120881,RMVar_hsa_circ_365756,RMVar_hsa_circ_245235,RMVar_hsa_circ_245237,RMVar_hsa_circ_90943,RMVar_hsa_circ_245236,RMVar_hsa_circ_245239,RMVar_hsa_circ_100762,RMVar_hsa_circ_245238 52200 RMVar_ID_52200 Human_SNP_ID_321776788 A-to-I Human chr7 + 56075918 56075918 56075918 CAGTCTAGCTCTGTCGCCCAAGGCTGGAGTACAGTGGCACGATCTCAGCTCCCTGCAACCTCCGC CAGTCTAGCTCTGTCGCCCAAGGCTGGAGTACGGTGGCACGATCTCAGCTCCCTGCAACCTCCGC A G SUMF2 Ensembl:ENSG00000129103 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1488375132 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95157,RMVar_hsa_circ_245233,RMVar_hsa_circ_107831,RMVar_hsa_circ_120881,RMVar_hsa_circ_365756,RMVar_hsa_circ_245235,RMVar_hsa_circ_245237,RMVar_hsa_circ_90943,RMVar_hsa_circ_245236,RMVar_hsa_circ_245239,RMVar_hsa_circ_100762,RMVar_hsa_circ_245238 52201 RMVar_ID_52201 Human_SNP_ID_321776803 A-to-I Human chr7 + 56075962 56075962 56075962 TCAGCTCCCTGCAACCTCCGCCTCCCGGGTTCAAGGGATTCTCCTGCCTCAGCCTCCCTAGTACC TCAGCTCCCTGCAACCTCCGCCTCCCGGGTTCGAGGGATTCTCCTGCCTCAGCCTCCCTAGTACC A G SUMF2 Ensembl:ENSG00000129103 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line - 31158229 RNA-Seq:(High) rs1412671974 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95157,RMVar_hsa_circ_245233,RMVar_hsa_circ_107831,RMVar_hsa_circ_120881,RMVar_hsa_circ_365756,RMVar_hsa_circ_245235,RMVar_hsa_circ_245237,RMVar_hsa_circ_90943,RMVar_hsa_circ_245236,RMVar_hsa_circ_245239,RMVar_hsa_circ_100762,RMVar_hsa_circ_245238 52202 RMVar_ID_52202 Human_SNP_ID_321777253 A-to-I Human chr7 + 56077574 56077574 56077574 TCCCAGCTGCTTGGGGCTTGGGCAGGAGAATCACTTGAACCCAGGAGGCGGAGGTTGCAGTGAGC TCCCAGCTGCTTGGGGCTTGGGCAGGAGAATCCCTTGAACCCAGGAGGCGGAGGTTGCAGTGAGC A C SUMF2 Ensembl:ENSG00000129103 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1304092487 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95157,RMVar_hsa_circ_245233,RMVar_hsa_circ_107831,RMVar_hsa_circ_365756,RMVar_hsa_circ_245235,RMVar_hsa_circ_245237,RMVar_hsa_circ_90943,RMVar_hsa_circ_111137,RMVar_hsa_circ_245239,RMVar_hsa_circ_100762,RMVar_hsa_circ_245238,RMVar_hsa_circ_277581,RMVar_hsa_circ_245240,RMVar_hsa_circ_245241 52203 RMVar_ID_52203 Human_SNP_ID_321777257 A-to-I Human chr7 + 56077584 56077584 56077584 TTGGGGCTTGGGCAGGAGAATCACTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCTACCACTGTA TTGGGGCTTGGGCAGGAGAATCACTTGAACCCGGGAGGCGGAGGTTGCAGTGAGCTACCACTGTA A G SUMF2 Ensembl:ENSG00000129103 Protein coding intron GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1431938062 Functional Loss SNV dbSNP153 33..33 33 - - - RMVar_hsa_circ_95157,RMVar_hsa_circ_245233,RMVar_hsa_circ_107831,RMVar_hsa_circ_365756,RMVar_hsa_circ_245235,RMVar_hsa_circ_245237,RMVar_hsa_circ_90943,RMVar_hsa_circ_111137,RMVar_hsa_circ_245239,RMVar_hsa_circ_100762,RMVar_hsa_circ_245238,RMVar_hsa_circ_277581,RMVar_hsa_circ_245240,RMVar_hsa_circ_245241 52204 RMVar_ID_52204 Human_SNP_ID_321777977 A-to-I Human chr7 + 56080155 56080155 56080155 ACATGTAACTATTTAAAGCACAGTTCAGTCCTAAAAGGGTCTGGGAGAACCAGATGATGTACTAG ACATGTAACTATTTAAAGCACAGTTCAGTCCTGAAAGGGTCTGGGAGAACCAGATGATGTACTAG A G SUMF2 Ensembl:ENSG00000129103 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs186076985 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_686235,Human_RBP_ID_2044411,Human_RBP_ID_16180803,Human_RBP_ID_17713306,Human_RBP_ID_26552379 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 52205 RMVar_ID_52205 Human_SNP_ID_321778043 A-to-I Human chr7 + 56080363 56080363 56080363 ACGGCTCACTCTAGCCTTGAATTCCTGGGCCCAAGCAATTCTCCCACCTCAGCCTCCTGAGTAGC ACGGCTCACTCTAGCCTTGAATTCCTGGGCCCCAGCAATTCTCCCACCTCAGCCTCCTGAGTAGC A C SUMF2 Ensembl:ENSG00000129103 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1314451594 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_686239,Human_RBP_ID_7746718,Human_RBP_ID_16180811,Human_RBP_ID_26551335 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 52206 RMVar_ID_52206 Human_SNP_ID_321778053 A-to-I Human chr7 + 56080403 56080403 56080403 CTCCCACCTCAGCCTCCTGAGTAGCTGGGACTACAAGTGTGCACCACCATGCCTGGCTAATTTTT CTCCCACCTCAGCCTCCTGAGTAGCTGGGACTGCAAGTGTGCACCACCATGCCTGGCTAATTTTT A G SUMF2 Ensembl:ENSG00000129103 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1179545479 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_686239 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 52207 RMVar_ID_52207 Human_SNP_ID_321778085 A-to-I Human chr7 + 56080525 56080525 56080525 GCCTCAAGCGATCCTCCCACCTCGACCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCTCGC GCCTCAAGCGATCCTCCCACCTCGACCTCCCAGAGTGCTGGGATTACAGGTGTGAGCCACCTCGC A G SUMF2 Ensembl:ENSG00000129103 Protein coding 3'UTR GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1369431857 Functional Loss SNV dbSNP153 33..33 33 - - - Human_RBP_ID_686243 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 52208 RMVar_ID_52208 Human_SNP_ID_321779313 A-to-I Human chr7 + 56084110 56084110 56084110 TTCCAGGCCAGGATGGCTAGAAGTGACCAGGGAAGCAATGGGCCCCGAGCTGGTGGCCCTGTGAG TTCCAGGCCAGGATGGCTAGAAGTGACCAGGGCAGCAATGGGCCCCGAGCTGGTGGCCCTGTGAG A C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1357866213 Functional Loss SNV dbSNP153 33..33 33 - - - 52209 RMVar_ID_52209 Human_SNP_ID_321779355 A-to-I Human chr7 + 56084204 56084204 56084204 GTTGGTGGACTTGGGAGAGTCCCAGCCCAAGCACCATTTCTGTTCCATCTCCATTGTATCAGTGT GTTGGTGGACTTGGGAGAGTCCCAGCCCAAGCGCCATTTCTGTTCCATCTCCATTGTATCAGTGT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs559800036 Functional Loss SNV dbSNP153 33..33 33 - - - 52210 RMVar_ID_52210 Human_SNP_ID_321780889 A-to-I Human chr7 + 56089542 56089542 56089542 GCGATCCTCACACCCTAGCCTCCTGAGTAGCTAGGACTAAAGTATCCCCCAGGCTGGAGTGCAGT GCGATCCTCACACCCTAGCCTCCTGAGTAGCTGGGACTAAAGTATCCCCCAGGCTGGAGTGCAGT A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1398646427 Functional Loss SNV dbSNP153 33..33 33 - - - 52211 RMVar_ID_52211 Human_SNP_ID_321783218 A-to-I Human chr7 - 56098067 56098067 56098067 TGCCACTGTGCCCAGTTAATTTTTGTATTTTTAGTAGGGACGGTTTCACCATGTTGGACAGGATG TGCCACTGTGCCCAGTTAATTTTTGTATTTTTGGTAGGGACGGTTTCACCATGTTGGACAGGATG T C - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs1017709492 Functional Loss SNV dbSNP153 33..33 33 - - - 52212 RMVar_ID_52212 Human_SNP_ID_321786132 A-to-I Human chr7 + 56107716 56107716 56107716 TACCTCGGCCTGCAAGGGCTGGGATTACAGGCATAAGCCACCAGGCCCAGCCTGAAATGCTTTCA TACCTCGGCCTGCAAGGGCTGGGATTACAGGCGTAAGCCACCAGGCCCAGCCTGAAATGCTTTCA A G - - Other Unknown GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs961914693 Functional Loss SNV dbSNP153 33..33 33 - - - 52213 RMVar_ID_52213 Human_SNP_ID_322058695 A-to-I Human chr7 - 57149569 57149569 57149569 TTGATTTTTTTGAAGAAGATCTCAGTGAGCACATAGTTCAAGGTGATGCCCTCCCTGGATGTGTG TTGATTTTTTTGAAGAAGATCTCAGTGAGCACTTAGTTCAAGGTGATGCCCTCCCTGGATGTGTG T A AC099654.2 Ensembl:ENSG00000235095 Pseudogene exon GSE100210 HepG2 cell line - 29129909 RNA-Seq:(High) rs973503576 Functional Loss SNV dbSNP153 33..33 33 - - - 52214 RMVar_ID_52214 Human_SNP_ID_800026179 A-to-I Human chr1 + 225786879 225786879 225786879 TTTTTTTTTTTTTAGAGACAGTGTCTTGCTCTATTGCTCAGGCTGCAGTGCAGTGGCATGATCAT TTTTTTTTTTTTTAGAGACAGTGTCTTGCTCTGTTGCTCAGGCTGCAGTGCAGTGGCATGATCAT A G SRP9 Ensembl:ENSG00000143742 Protein coding CDS GSE38233;GSE56152;GSE100210 cultured B-cells;embryonic stem cells,wild type;HepG2 cell line chr1:225786878..225786879 24183664,25708366,29129909 RNA-Seq:(High) rs1161553517 Functional Loss SNV ICGC 33..33 33 BRCA 1 - Human_RBP_ID_10807870,Human_RBP_ID_17557432,Human_RBP_ID_23368629 Human_Splice_Rec_192742,Human_Splice_Rec_192758,Human_Splice_Rec_192764,Human_Splice_Rec_192776 Human_miRNA_ID_2577930,Human_miRNA_ID_2676647 RMVar_hsa_circ_35495,RMVar_hsa_circ_100395,RMVar_hsa_circ_140051,RMVar_hsa_circ_140054,RMVar_hsa_circ_84583 52215 RMVar_ID_52215 Human_SNP_ID_800077540 A-to-I Human chr1 + 32652667 32652667 32652667 GATTCGAGCGATTCTCCTGCCTAAGCCCTCCCAAGTAGCTGGGATTACAGGCACCTGCCACCACG GATTCGAGCGATTCTCCTGCCTAAGCCCTCCCGAGTAGCTGGGATTACAGGCACCTGCCACCACG A G RBBP4 Ensembl:ENSG00000162521 Protein coding intron GSE100210 HepG2 cell line chr1:32652666..32652667 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_131272,RMVar_hsa_circ_309059,RMVar_hsa_circ_366909,RMVar_hsa_circ_370393,RMVar_hsa_circ_131273,RMVar_hsa_circ_378233 52216 RMVar_ID_52216 Human_SNP_ID_800111652 A-to-I Human chr1 + 62162857 62162855 62162857 TAATCCCAGCTACTCCGGAGGTTGAAGCAGGAAAATTGCTTGAACCTGGGAGGTGGAGGTTGCAG TAATCCCAGCTACTCCGGAGGTTGAAGCAGG__AATTGCTTGAACCTGGGAGGTGGAGGTTGCAG GAA G PATJ Ensembl:ENSG00000132849 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells chr1:62162857..62162858 23474544 RNA-Seq:(High) - Functional Loss DEL ICGC 32..33 33 LICA 1 - 52217 RMVar_ID_52217 Human_SNP_ID_800111652 A-to-I Human chr1 + 62162856 62162855 62162857 GTAATCCCAGCTACTCCGGAGGTTGAAGCAGGAAAATTGCTTGAACCTGGGAGGTGGAGGTTGCA GTAATCCCAGCTACTCCGGAGGTTGAAGCAGG__AATTGCTTGAACCTGGGAGGTGGAGGTTGCA GAA G PATJ Ensembl:ENSG00000132849 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells chr1:62162856..62162857 23474544 RNA-Seq:(High) - Functional Loss DEL ICGC 33..34 33 LICA 1 - 52218 RMVar_ID_52218 Human_SNP_ID_800179959 A-to-I Human chr1 + 151079757 151079757 151079757 TGTCTGTACTAAGAATACAAAATTAGCTGGGCATGGTGACACATGCCTGTAATACCAGCTACTCG TGTCTGTACTAAGAATACAAAATTAGCTGGGCGTGGTGACACATGCCTGTAATACCAGCTACTCG A G GABPB2 Ensembl:ENSG00000143458 Protein coding intron GSE100210 HepG2 cell line chr1:151079756..151079757 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 2 breast 52219 RMVar_ID_52219 Human_SNP_ID_800223371 A-to-I Human chr1 - 114445996 114445996 114445996 AAAATTAGCTGGGCGTGGGAACATGTGCCTGTAGTCCCAGCTACCTGGGAGGCTGAGGCAGGAGA AAAATTAGCTGGGCGTGGGAACATGTGCCTGTTGTCCCAGCTACCTGGGAGGCTGAGGCAGGAGA T A TRIM33 Ensembl:ENSG00000197323 Protein coding intron GSE100210 HepG2 cell line chr1:114445995..114445996 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_135537,RMVar_hsa_circ_285034,RMVar_hsa_circ_375416,RMVar_hsa_circ_135538,RMVar_hsa_circ_77064,RMVar_hsa_circ_135539,RMVar_hsa_circ_135540,RMVar_hsa_circ_370046 52220 RMVar_ID_52220 Human_SNP_ID_800242823 A-to-I Human chr1 - 155670937 155670937 155670937 GGCCGGGCGCCGTGGCTTACGCCTGTAATCCAACACTTTAGGAGGCCGAGGCTGTCGGATGACAA GGCCGGGCGCCGTGGCTTACGCCTGTAATCCAGCACTTTAGGAGGCCGAGGCTGTCGGATGACAA T C YY1AP1 Ensembl:ENSG00000163374 Protein coding intron GSE38233 cultured B-cells chr1:155670936..155670937 24183664 RNA-Seq:(High) rs12728041 Functional Loss SNV ICGC 33..33 33 LAML 1 - RMVar_hsa_circ_6989,RMVar_hsa_circ_78938,RMVar_hsa_circ_26391,RMVar_hsa_circ_68465,RMVar_hsa_circ_136652,RMVar_hsa_circ_297077,RMVar_hsa_circ_324879,RMVar_hsa_circ_40466,RMVar_hsa_circ_136660,RMVar_hsa_circ_291675,RMVar_hsa_circ_136655,RMVar_hsa_circ_136656,RMVar_hsa_circ_136654,RMVar_hsa_circ_339529,RMVar_hsa_circ_340434,RMVar_hsa_circ_323095,RMVar_hsa_circ_273574,RMVar_hsa_circ_289095,RMVar_hsa_circ_136658,RMVar_hsa_circ_136659 52221 RMVar_ID_52221 Human_SNP_ID_800272224 A-to-I Human chr1 - 243160064 243160064 243160064 AACAACTTGGCTGGGCACAGCGTCTCATGACTATAATCCTAGGACTTTGGGAGGCTGAGGCAGAT AACAACTTGGCTGGGCACAGCGTCTCATGACTGTAATCCTAGGACTTTGGGAGGCTGAGGCAGAT T C CEP170 Ensembl:ENSG00000143702 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr1:243160063..243160064 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_10872248,Human_RBP_ID_24361225 RMVar_hsa_circ_67961,RMVar_hsa_circ_141116,RMVar_hsa_circ_123009,RMVar_hsa_circ_361806,RMVar_hsa_circ_376631,RMVar_hsa_circ_318724,RMVar_hsa_circ_141119,RMVar_hsa_circ_67753,RMVar_hsa_circ_48457,RMVar_hsa_circ_141117,RMVar_hsa_circ_141118 52222 RMVar_ID_52222 Human_SNP_ID_800280485 A-to-I Human chr1 - 50751025 50751025 50751025 TCACTGTACATCCCCATATTAGTATAGTAAATAAGAAAAAGCATTTGACAATATTCAACACCCAT TCACTGTACATCCCCATATTAGTATAGTAAATGAGAAAAAGCATTTGACAATATTCAACACCCAT T C FAF1 Ensembl:ENSG00000185104 Protein coding intron GSE100210 HepG2 cell line chr1:50751024..50751025 29129909 RNA-Seq:(High) rs1293379392 Functional Loss SNV ICGC 33..33 33 PAAD 1 - RMVar_hsa_circ_121195,RMVar_hsa_circ_57665,RMVar_hsa_circ_132749,RMVar_hsa_circ_62423,RMVar_hsa_circ_266772,RMVar_hsa_circ_713,RMVar_hsa_circ_349107,RMVar_hsa_circ_374256,RMVar_hsa_circ_3800,RMVar_hsa_circ_132772,RMVar_hsa_circ_335009,RMVar_hsa_circ_352666,RMVar_hsa_circ_132778,RMVar_hsa_circ_296031,RMVar_hsa_circ_302367,RMVar_hsa_circ_340641,RMVar_hsa_circ_132780,RMVar_hsa_circ_132781,RMVar_hsa_circ_132779,RMVar_hsa_circ_311315 52223 RMVar_ID_52223 Human_SNP_ID_800307374 A-to-I Human chr1 - 23327568 23327568 23327568 CTTCTGCCTAAGCCTCCAGAGTAGCTGGGATTACAGGCTTGTGCCACCATGCCTGACTAATTTTT CTTCTGCCTAAGCCTCCAGAGTAGCTGGGATTGCAGGCTTGTGCCACCATGCCTGACTAATTTTT T C HNRNPR Ensembl:ENSG00000125944 Protein coding intron GSE47997 K562 cells&HepG2 cells chr1:23327567..23327568 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_557,RMVar_hsa_circ_67146,RMVar_hsa_circ_55437,RMVar_hsa_circ_356207,RMVar_hsa_circ_305724,RMVar_hsa_circ_292881,RMVar_hsa_circ_320103,RMVar_hsa_circ_371291,RMVar_hsa_circ_130450 52224 RMVar_ID_52224 Human_SNP_ID_800334857 A-to-I Human chr1 - 151317437 151317437 151317437 AGGCACATGCGTGTAGTCCTGGATACTTGGGAAGCTGAGGTAGGAGGATTGCTTGAGCCCAGAAA AGGCACATGCGTGTAGTCCTGGATACTTGGGATGCTGAGGTAGGAGGATTGCTTGAGCCCAGAAA T A PI4KB Ensembl:ENSG00000143393 Protein coding intron GSE100210 HepG2 cell line chr1:151317436..151317437 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - RMVar_hsa_circ_44726,RMVar_hsa_circ_348638,RMVar_hsa_circ_345443 52225 RMVar_ID_52225 Human_SNP_ID_800362578 A-to-I Human chr1 + 22083115 22083115 22083115 GTTGGTCAGGCTGGTCTCGAACTTCTGACCTCAGGTGATCCGCCCGCCTTGGCCTCCCAAAGTGC GTTGGTCAGGCTGGTCTCGAACTTCTGACCTCGGGTGATCCGCCCGCCTTGGCCTCCCAAAGTGC A G CDC42 Ensembl:ENSG00000070831 Protein coding intron GSE38233 cultured B-cells chr1:22083114..22083115 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - RMVar_hsa_circ_97695,RMVar_hsa_circ_103628,RMVar_hsa_circ_342544,RMVar_hsa_circ_130355,RMVar_hsa_circ_378086,RMVar_hsa_circ_345538,RMVar_hsa_circ_276873,RMVar_hsa_circ_100439,RMVar_hsa_circ_104993,RMVar_hsa_circ_130356,RMVar_hsa_circ_130357,RMVar_hsa_circ_130358,RMVar_hsa_circ_127635,RMVar_hsa_circ_130359,RMVar_hsa_circ_130360,RMVar_hsa_circ_130362 52226 RMVar_ID_52226 Human_SNP_ID_800368674 A-to-I Human chr1 + 10139243 10139243 10139243 CATAGTGAAAACCCGTCTCTACTACAAAAATTAGCTGGGCATGGTTGGCGCATGCCTGTAATCCC CATAGTGAAAACCCGTCTCTACTACAAAAATTGGCTGGGCATGGTTGGCGCATGCCTGTAATCCC A G UBE4B Ensembl:ENSG00000130939 Protein coding intron GSE100210 HepG2 cell line chr1:10139242..10139243 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - RMVar_hsa_circ_90073,RMVar_hsa_circ_128859,RMVar_hsa_circ_34341,RMVar_hsa_circ_128867,RMVar_hsa_circ_373995,RMVar_hsa_circ_343797,RMVar_hsa_circ_351489,RMVar_hsa_circ_303123,RMVar_hsa_circ_278777,RMVar_hsa_circ_25726,RMVar_hsa_circ_267445,RMVar_hsa_circ_7080,RMVar_hsa_circ_68860,RMVar_hsa_circ_128873,RMVar_hsa_circ_46870,RMVar_hsa_circ_28713,RMVar_hsa_circ_68846,RMVar_hsa_circ_43636,RMVar_hsa_circ_325027,RMVar_hsa_circ_377580,RMVar_hsa_circ_370641,RMVar_hsa_circ_128884,RMVar_hsa_circ_128885,RMVar_hsa_circ_44472,RMVar_hsa_circ_1895,RMVar_hsa_circ_128887,RMVar_hsa_circ_367134 52227 RMVar_ID_52227 Human_SNP_ID_800383663 A-to-I Human chr1 + 198266727 198266727 198266727 TGTTATGATGGTTAAGTAATATAATATATAGTATGTTTATATATATACTTTTTAAAGACATATGT TGTTATGATGGTTAAGTAATATAATATATAGTGTGTTTATATATATACTTTTTAAAGACATATGT A G NEK7 Ensembl:ENSG00000151414 Protein coding intron GSE100210 HepG2 cell line chr1:198266726..198266727 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_23354596 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 52228 RMVar_ID_52228 Human_SNP_ID_800387816 A-to-I Human chr1 - 233057764 233057764 233057764 CCTCGGCCTCCTGGATTCAAGTTCAGCCTCCCAAGTAGCTGAGATTATAGGAGTGTGCCACCACA CCTCGGCCTCCTGGATTCAAGTTCAGCCTCCCTAGTAGCTGAGATTATAGGAGTGTGCCACCACA T A PCNX2 Ensembl:ENSG00000135749 Protein coding intron GSE47997 K562 cells&HepG2 cells chr1:233057763..233057764 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_2219,RMVar_hsa_circ_75934,RMVar_hsa_circ_80113,RMVar_hsa_circ_85264,RMVar_hsa_circ_140487,RMVar_hsa_circ_370343,RMVar_hsa_circ_117173,RMVar_hsa_circ_140490,RMVar_hsa_circ_140491,RMVar_hsa_circ_91439,RMVar_hsa_circ_113594,RMVar_hsa_circ_140493,RMVar_hsa_circ_140495,RMVar_hsa_circ_81895,RMVar_hsa_circ_140494,RMVar_hsa_circ_140492,RMVar_hsa_circ_324199,RMVar_hsa_circ_378777,RMVar_hsa_circ_140496,RMVar_hsa_circ_140502,RMVar_hsa_circ_96071,RMVar_hsa_circ_97696,RMVar_hsa_circ_76957,RMVar_hsa_circ_105697,RMVar_hsa_circ_140504,RMVar_hsa_circ_140505,RMVar_hsa_circ_140503,RMVar_hsa_circ_267179,RMVar_hsa_circ_26396,RMVar_hsa_circ_140508,RMVar_hsa_circ_12377,RMVar_hsa_circ_321569,RMVar_hsa_circ_365762,RMVar_hsa_circ_374338,RMVar_hsa_circ_374339,RMVar_hsa_circ_321736,RMVar_hsa_circ_301125,RMVar_hsa_circ_275025,RMVar_hsa_circ_52052,RMVar_hsa_circ_59902,RMVar_hsa_circ_24513,RMVar_hsa_circ_140518,RMVar_hsa_circ_140511,RMVar_hsa_circ_140513,RMVar_hsa_circ_140514,RMVar_hsa_circ_140512,RMVar_hsa_circ_119558,RMVar_hsa_circ_140510,RMVar_hsa_circ_76435,RMVar_hsa_circ_140517 52229 RMVar_ID_52229 Human_SNP_ID_800388726 A-to-I Human chr1 - 19608385 19608385 19608385 CTCCTGTGGCCCGGAGTTGGATGTGTAGGGCAATGATACCCAGCTCCTTGCACCTCTGGGCCACA CTCCTGTGGCCCGGAGTTGGATGTGTAGGGCAGTGATACCCAGCTCCTTGCACCTCTGGGCCACA T C - - Other Unknown GSE100210 HepG2 cell line chr1:19608384..19608385 29129909 RNA-Seq:(High) rs779101275 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 8 haematopoietic and lymphoid tissue 52230 RMVar_ID_52230 Human_SNP_ID_800393992 A-to-I Human chr1 - 71685510 71685510 71685510 CAAGAGCAGGCTGGCCAATATGGTGAAACCCCATCTTTACTAAAAATACAAAAGTAGCCAGGTGT CAAGAGCAGGCTGGCCAATATGGTGAAACCCCGTCTTTACTAAAAATACAAAAGTAGCCAGGTGT T C NEGR1 Ensembl:ENSG00000172260 Protein coding intron GSE47997 K562 cells&HepG2 cells chr1:71685509..71685510 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_15617,RMVar_hsa_circ_334592 52231 RMVar_ID_52231 Human_SNP_ID_800424210 A-to-I Human chr1 - 154483951 154483951 154483951 CTGTGTTGCCCAGGCTGGAGTGCAATGGCGCAATCTTGGCTCACTGCAACATCTGACTCCTGGGT CTGTGTTGCCCAGGCTGGAGTGCAATGGCGCAGTCTTGGCTCACTGCAACATCTGACTCCTGGGT T C SHE Ensembl:ENSG00000169291 Protein coding intron GSE47997 K562 cells&HepG2 cells chr1:154483950..154483951 23474544 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 3 liver 52232 RMVar_ID_52232 Human_SNP_ID_800436412 A-to-I Human chr1 + 84149353 84149353 84149353 GGGATTTCGACTCGCTGCAGCCTCTGCCTCCCAGGCTCAAGCGATCCTCCCATCTCAGTTTCCCA GGGATTTCGACTCGCTGCAGCCTCTGCCTCCCGGGCTCAAGCGATCCTCCCATCTCAGTTTCCCA A G PRKACB Ensembl:ENSG00000142875 Protein coding intron GSE100210 HepG2 cell line chr1:84149352..84149353 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 4 ovary 52233 RMVar_ID_52233 Human_SNP_ID_800440686 A-to-I Human chr1 - 225865012 225865012 225865012 GACTTAAGGCATCTTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTGCAGACACATGGCACCACAC GACTTAAGGCATCTTCCTGCCTCAGCCTCCCATGTAGCTGGGACTGCAGACACATGGCACCACAC T A TMEM63A Ensembl:ENSG00000196187 Protein coding intron GSE100210 HepG2 cell line chr1:225865011..225865012 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 STAD 1 - RMVar_hsa_circ_55460,RMVar_hsa_circ_23341,RMVar_hsa_circ_77294,RMVar_hsa_circ_33471,RMVar_hsa_circ_349997,RMVar_hsa_circ_80737,RMVar_hsa_circ_140060,RMVar_hsa_circ_140061 52234 RMVar_ID_52234 Human_SNP_ID_800520067 A-to-I Human chr1 - 155371799 155371799 155371799 ATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCTCTTGAACCTGGGAAGCGGAGTTTGCAGTG ATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAGTCTCTTGAACCTGGGAAGCGGAGTTTGCAGTG T C ASH1L Ensembl:ENSG00000116539 Protein coding intron GSE38233 cultured B-cells chr1:155371798..155371799 24183664 RNA-Seq:(High) rs935490878 Functional Loss SNV ICGC 33..33 33 PAAD 1 - RMVar_hsa_circ_42667,RMVar_hsa_circ_368935,RMVar_hsa_circ_366827,RMVar_hsa_circ_358498,RMVar_hsa_circ_69363,RMVar_hsa_circ_55904,RMVar_hsa_circ_136579,RMVar_hsa_circ_91291,RMVar_hsa_circ_136577,RMVar_hsa_circ_370041,RMVar_hsa_circ_356619,RMVar_hsa_circ_91812,RMVar_hsa_circ_55595,RMVar_hsa_circ_136580,RMVar_hsa_circ_106304,RMVar_hsa_circ_67956,RMVar_hsa_circ_136588,RMVar_hsa_circ_107116,RMVar_hsa_circ_136592,RMVar_hsa_circ_78519,RMVar_hsa_circ_36517,RMVar_hsa_circ_71110,RMVar_hsa_circ_136595,RMVar_hsa_circ_136594,RMVar_hsa_circ_110760,RMVar_hsa_circ_97081,RMVar_hsa_circ_360900,RMVar_hsa_circ_136598,RMVar_hsa_circ_11734,RMVar_hsa_circ_136603,RMVar_hsa_circ_85679,RMVar_hsa_circ_42461,RMVar_hsa_circ_136606,RMVar_hsa_circ_55666,RMVar_hsa_circ_357101,RMVar_hsa_circ_118802,RMVar_hsa_circ_136607,RMVar_hsa_circ_22549,RMVar_hsa_circ_102723,RMVar_hsa_circ_59208,RMVar_hsa_circ_66639,RMVar_hsa_circ_136610,RMVar_hsa_circ_363166,RMVar_hsa_circ_285466,RMVar_hsa_circ_61432,RMVar_hsa_circ_332675,RMVar_hsa_circ_136612,RMVar_hsa_circ_136613,RMVar_hsa_circ_343437,RMVar_hsa_circ_318341,RMVar_hsa_circ_298012,RMVar_hsa_circ_136616,RMVar_hsa_circ_136617,RMVar_hsa_circ_136618,RMVar_hsa_circ_136615 52235 RMVar_ID_52235 Human_SNP_ID_800527028 A-to-I Human chr1 + 78020073 78020073 78020073 TACTTGGGAGGCTAAGGCAGGAGAATCGCTTGAACCTGGGAGGTGGAGGTTGCAATGAGCTGACA TACTTGGGAGGCTAAGGCAGGAGAATCGCTTGGACCTGGGAGGTGGAGGTTGCAATGAGCTGACA A G GIPC2 Ensembl:ENSG00000137960 Protein coding intron GSE100210 HepG2 cell line chr1:78020073..78020074 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 52236 RMVar_ID_52236 Human_SNP_ID_800550416 A-to-I Human chr1 + 39031442 39031442 39031442 GTCATCCTCCTGCCTCAGCCTCCCAAGTAGCTAGGACTACAAGTGCATGCCACCATGTGCGGCTT GTCATCCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAAGTGCATGCCACCATGTGCGGCTT A G NDUFS5 Ensembl:ENSG00000168653 Protein coding intron GSE38233 cultured B-cells chr1:39031441..39031442 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - RMVar_hsa_circ_113812,RMVar_hsa_circ_131807 52237 RMVar_ID_52237 Human_SNP_ID_800559031 A-to-I Human chr1 - 160217677 160217677 160217677 GCGCTGGCGAGAACCTGGGGTTGGGGCCACAGACGCGGACTCTGATGAGTCTCCCAGCTCCTCAG GCGCTGGCGAGAACCTGGGGTTGGGGCCACAGGCGCGGACTCTGATGAGTCTCCCAGCTCCTCAG T C DCAF8,AL139011.2 Ensembl:ENSG00000132716,Ensembl:ENSG00000258465 Protein coding,Protein coding CDS,3'UTR GSE100210 HepG2 cell line chr1:160217676..160217677 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,right_upper_lobe adenocarcinoma,LUAD 6 lung Human_RBP_ID_221888,Human_RBP_ID_855432,Human_RBP_ID_1727346,Human_RBP_ID_5699214,Human_RBP_ID_10613931 Human_Splice_Rec_147196,Human_Splice_Rec_147222,Human_Splice_Rec_147248,Human_Splice_Rec_147254,Human_Splice_Rec_147255,Human_Splice_Rec_147260,Human_Splice_Rec_147286,Human_Splice_Rec_147298,Human_Splice_Rec_147304,Human_Splice_Rec_147380,Human_Splice_Rec_147414 RMVar_hsa_circ_93317,RMVar_hsa_circ_123319,RMVar_hsa_circ_103147,RMVar_hsa_circ_137002,RMVar_hsa_circ_137003,RMVar_hsa_circ_137004 52238 RMVar_ID_52238 Human_SNP_ID_800567886 A-to-I Human chr1 + 38709526 38709526 38709526 CTAAATGTTATGAGGATCATCAATAAGCCTACAGCAGCTGCTATTGCTTATGGCCTGGATAAGAG CTAAATGTTATGAGGATCATCAATAAGCCTACGGCAGCTGCTATTGCTTATGGCCTGGATAAGAG A G HSPA5P1 Ensembl:ENSG00000215895 Pseudogene exon GSE100210 HepG2 cell line chr1:38709525..38709526 29129909 RNA-Seq:(High) rs766464340 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_8242510 Human_miRNA_ID_1870297,Human_miRNA_ID_1876302,Human_miRNA_ID_1876494,Human_miRNA_ID_1878549 52239 RMVar_ID_52239 Human_SNP_ID_800568807 A-to-I Human chr1 + 149887584 149887584 149887584 TCCGTTTTCTTGGGCAACAGGACAGCCTGGATATTGGGCAAGACGCCGCCCTGGGCAATGGTGAC TCCGTTTTCTTGGGCAACAGGACAGCCTGGATTTTGGGCAAGACGCCGCCCTGGGCAATGGTGAC A T - - Other Unknown GSE100210 HepG2 cell line chr1:149887583..149887584 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - 52240 RMVar_ID_52240 Human_SNP_ID_800572068 A-to-I Human chr1 + 63421256 63421256 63421256 GCTGGAGTGCAATAGCGTGATCTTGGCTCACCACAACCTCCGCCTCCCTAGTTCAAGCGATTCTC GCTGGAGTGCAATAGCGTGATCTTGGCTCACCGCAACCTCCGCCTCCCTAGTTCAAGCGATTCTC A G ALG6 Ensembl:ENSG00000088035 Protein coding intron GSE38233 cultured B-cells chr1:63421255..63421256 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - Human_RBP_ID_9534069 RMVar_hsa_circ_34288,RMVar_hsa_circ_323317,RMVar_hsa_circ_304283,RMVar_hsa_circ_133590,RMVar_hsa_circ_133591 52241 RMVar_ID_52241 Human_SNP_ID_800580008 A-to-I Human chr1 + 9267999 9267999 9267999 TAGGTGTGGCTCATGCCTGTAATCCCAGCACTATGGGAGGCTGAGGTGAGAGGATCACTTGAGCC TAGGTGTGGCTCATGCCTGTAATCCCAGCACTGTGGGAGGCTGAGGTGAGAGGATCACTTGAGCC A G H6PD Ensembl:ENSG00000049239 Protein coding 3'UTR GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line chr1:9267998..9267999 32596459 RNA-Seq:(High) rs1002730146 Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 1 kidney Human_Splice_Rec_14711 RMVar_hsa_circ_113746,RMVar_hsa_circ_94938,RMVar_hsa_circ_128797,RMVar_hsa_circ_128800,RMVar_hsa_circ_123281,RMVar_hsa_circ_128801 52242 RMVar_ID_52242 Human_SNP_ID_800601628 A-to-I Human chr1 + 147204351 147204351 147204351 CAAACTCTGATGTTATCAACTTTGAAATGGCCAGAATCAGGAAAAATAGATACGCATGCCTGAAC CAAACTCTGATGTTATCAACTTTGAAATGGCCGGAATCAGGAAAAATAGATACGCATGCCTGAAC A G AC242426.2 Ensembl:ENSG00000237188 lincRNA intron GSE100210 HepG2 cell line chr1:147204350..147204351 29129909 RNA-Seq:(High) rs879971059 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 10 haematopoietic and lymphoid tissue 52243 RMVar_ID_52243 Human_SNP_ID_800601698 A-to-I Human chr1 + 36069251 36069221 36069252 TCAGCCTCCCAAGTAGCTGGGACTAGAGGTACATGCCACCACACCCAGCTAATTATTTTCTTTTA TCA_______________________________GCCACCACACCCAGCTAATTATTTTCTTTTA AGCCTCCCAAGTAGCTGGGACTAGAGGTACAT A AGO3 Ensembl:ENSG00000126070 Protein coding 3'UTR GSE100210 HepG2 cell line chr1:36069250..36069251 29129909 RNA-Seq:(High) rs369399300 Functional Loss DEL ICGC 4..34 33 PBCA 1 - 52244 RMVar_ID_52244 Human_SNP_ID_800613049 A-to-I Human chr1 + 32683907 32683907 32683907 CACCCTCCTCAGCCTCCCAAAGTGCTAGGATTACAGGCGTGAGCCACCCCGTCCGGCCTGTTTTT CACCCTCCTCAGCCTCCCAAAGTGCTAGGATTGCAGGCGTGAGCCACCCCGTCCGGCCTGTTTTT A G RBBP4 Ensembl:ENSG00000162521 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line chr1:32683906..32683907 23474544,24183664,29129909,31158229 RNA-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_24764248 52245 RMVar_ID_52245 Human_SNP_ID_800616694 A-to-I Human chr1 - 214528739 214528739 214528739 TTTAGTAGAGATGGAGTTTCACCATATTGGCCAAACTGGTCTTGAACTCCTGACTTCCAGTGATC TTTAGTAGAGATGGAGTTTCACCATATTGGCCGAACTGGTCTTGAACTCCTGACTTCCAGTGATC T C PTPN14 Ensembl:ENSG00000152104 Protein coding intron GSE47997 K562 cells&HepG2 cells chr1:214528738..214528739 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma,CLLE 3 haematopoietic and lymphoid tissue 52246 RMVar_ID_52246 Human_SNP_ID_800674704 A-to-I Human chr1 + 19333362 19333362 19333362 CACCACGCCCAGCTAGTTTTTGTATTTTTGGTAGAGATGGGGTTTCGCCATGTTGCCCAGCAGGC CACCACGCCCAGCTAGTTTTTGTATTTTTGGTGGAGATGGGGTTTCGCCATGTTGCCCAGCAGGC A G lnc-PQLC2-1 RNACentral:URS00008B65DF lincRNA intron GSE100210 HepG2 cell line chr1:19333361..19333362 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 52247 RMVar_ID_52247 Human_SNP_ID_800674752 A-to-I Human chr1 - 6223216 6223214 6223217 GTAATCCCAGCTACTCAGGAGGCTGAGACAGGAGAATCCTTTGAACCCAGGAGGCGGAGGTTGCA GTAATCCCAGCTACTCAGGAGGCTGAGACAG___AATCCTTTGAACCCAGGAGGCGGAGGTTGCA TCTC T ICMT Ensembl:ENSG00000116237 Protein coding 3'UTR GSE100210 HepG2 cell line chr1:6223215..6223216 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 32..34 33 ESCA 1 - RMVar_hsa_circ_98828,RMVar_hsa_circ_123631,RMVar_hsa_circ_103272,RMVar_hsa_circ_128612,RMVar_hsa_circ_128613,RMVar_hsa_circ_128611 52248 RMVar_ID_52248 Human_SNP_ID_800696517 A-to-I Human chr1 + 220467992 220467992 220467992 ATCTGGACTTCGGAGCACGTCTTTGACCACCCATAGGAAACTGTTACAACAGCTGCAATGCAGAA ATCTGGACTTCGGAGCACGTCTTTGACCACCCGTAGGAAACTGTTACAACAGCTGCAATGCAGAA A G PRELID3BP1 Ensembl:ENSG00000226226 Pseudogene exon GSE100210 HepG2 cell line chr1:220467991..220467992 29129909 RNA-Seq:(High) rs757389142 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_17339372,Human_RBP_ID_26375665 Human_miRNA_ID_1835879,Human_miRNA_ID_1838730 52249 RMVar_ID_52249 Human_SNP_ID_800704355 A-to-I Human chr1 - 16689354 16689354 16689354 CAAAAATTAGCTGGGCATGGTGGCACGCTCCTATAATCCCAGCTACTCAGAAGGCTGAGGCAGGA CAAAAATTAGCTGGGCATGGTGGCACGCTCCTGTAATCCCAGCTACTCAGAAGGCTGAGGCAGGA T C ESPNP Ensembl:ENSG00000268869 Pseudogene intron GSE100210 HepG2 cell line chr1:16689353..16689354 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 52250 RMVar_ID_52250 Human_SNP_ID_800787746 A-to-I Human chr1 + 173362852 173362852 173362852 CAATGCAAGACAAGCTGAACATTGGCTGCCACAGCATGGCTAAGACTTGTGGACTTCCCAGCTAC CAATGCAAGACAAGCTGAACATTGGCTGCCACGGCATGGCTAAGACTTGTGGACTTCCCAGCTAC A G - - Other Unknown GSE100210 HepG2 cell line chr1:173362851..173362852 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 52251 RMVar_ID_52251 Human_SNP_ID_800799163 A-to-I Human chr1 - 240143466 240143466 240143466 AAAGGCAAGAAGGAAAAGAAGGACAAGGACAAAAAGGAAACCCCTGCTGACATGGGAGCACATCA AAAGGCAAGAAGGAAAAGAAGGACAAGGACAAGAAGGAAACCCCTGCTGACATGGGAGCACATCA T C AL359918.2 Ensembl:ENSG00000228818 Pseudogene exon GSE100210 HepG2 cell line chr1:240143465..240143466 29129909 RNA-Seq:(High) rs879153590 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue Human_miRNA_ID_1841305,Human_miRNA_ID_1844317,Human_miRNA_ID_1862797,Human_miRNA_ID_1908532 52252 RMVar_ID_52252 Human_SNP_ID_800821718 A-to-I Human chr1 + 40570690 40570690 40570690 AAATTTGGCCGGGCGTGGTGGTGCGCGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCACAAGA AAATTTGGCCGGGCGTGGTGGTGCGCGCCTGTCGTCCCAGCTACTCAGGAGGCTGAGGCACAAGA A C - - Other Unknown GSE100210 HepG2 cell line chr1:40570689..40570690 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - 52253 RMVar_ID_52253 Human_SNP_ID_800838665 A-to-I Human chr1 - 205738821 205738821 205738821 GCACTGCAACCTCCGCCTCCCAGGCTCAAGCTATTCTCCCACCTCAGCCCCTGGAGTGGCTGGGA GCACTGCAACCTCCGCCTCCCAGGCTCAAGCTGTTCTCCCACCTCAGCCCCTGGAGTGGCTGGGA T C NUCKS1 Ensembl:ENSG00000069275 Protein coding intron GSE100210 HepG2 cell line chr1:205738820..205738821 29129909 RNA-Seq:(High) rs1006246382 Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 2 prostate 52254 RMVar_ID_52254 Human_SNP_ID_800841286 A-to-I Human chr1 + 161214301 161214301 161214301 CTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGTTCATGTACACTTGGCTGTCAGGCTTTCTG CTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTCATGTACACTTGGCTGTCAGGCTTTCTG A G NDUFS2 Ensembl:ENSG00000158864 Protein coding 3'UTR GSE100210 HepG2 cell line chr1:161214300..161214301 29129909 RNA-Seq:(High) rs191955041 Functional Loss SNV ICGC,COSMIC 33..33 33 prostate adenocarcinoma,LICA,liver neoplasm,cervix squamous_cell_carcinoma 7 uterus,liver,prostate Human_RBP_ID_21958,Human_RBP_ID_330296,Human_RBP_ID_972068,Human_RBP_ID_1074500,Human_RBP_ID_1414034,Human_RBP_ID_1727528,Human_RBP_ID_4083610,Human_RBP_ID_5136420,Human_RBP_ID_5278588,Human_RBP_ID_5641850,Human_RBP_ID_8288202,Human_RBP_ID_17222853,Human_RBP_ID_17646580,Human_RBP_ID_18554230,Human_RBP_ID_22705519,Human_RBP_ID_22749565,Human_RBP_ID_22872905,Human_RBP_ID_23112385,Human_RBP_ID_23205407,Human_RBP_ID_23338721,Human_RBP_ID_26370424,Human_RBP_ID_26844853,Human_RBP_ID_27170400 Human_miRNA_ID_2728697 Clinvar_Rec_112 RMVar_hsa_circ_113883,RMVar_hsa_circ_137142 52255 RMVar_ID_52255 Human_SNP_ID_800863646 A-to-I Human chr1 - 29204150 29204150 29204150 CAGTGGCGCGATCTCAGCTCACTGCAACCTCCACCTCCCGGGTTCAAGCGATTCTCCTGCCTCAG CAGTGGCGCGATCTCAGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCAG T C MECR Ensembl:ENSG00000116353 Protein coding intron GSE47997 K562 cells&HepG2 cells chr1:29204149..29204150 23474544 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 2 prostate RMVar_hsa_circ_26754,RMVar_hsa_circ_353558,RMVar_hsa_circ_79279,RMVar_hsa_circ_6218,RMVar_hsa_circ_130945,RMVar_hsa_circ_130947,RMVar_hsa_circ_370288,RMVar_hsa_circ_55808,RMVar_hsa_circ_130948 52256 RMVar_ID_52256 Human_SNP_ID_800867980 A-to-I Human chr1 - 11120367 11120367 11120367 TGTGGGTTAATTTTTGTATTCTTAGTAGAGACAGGGTTTCACCATGTTGTCCAGGCTAGTCTCAA TGTGGGTTAATTTTTGTATTCTTAGTAGAGACGGGGTTTCACCATGTTGTCCAGGCTAGTCTCAA T C MTOR Ensembl:ENSG00000198793 Protein coding intron GSE38233 cultured B-cells chr1:11120366..11120367 24183664 RNA-Seq:(High) rs889142773 Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_1741,RMVar_hsa_circ_98592,RMVar_hsa_circ_102553,RMVar_hsa_circ_129068,RMVar_hsa_circ_98908,RMVar_hsa_circ_129067,RMVar_hsa_circ_100586,RMVar_hsa_circ_370450,RMVar_hsa_circ_129069,RMVar_hsa_circ_129073,RMVar_hsa_circ_87622,RMVar_hsa_circ_129074,RMVar_hsa_circ_129072,RMVar_hsa_circ_52865,RMVar_hsa_circ_75310,RMVar_hsa_circ_90661,RMVar_hsa_circ_86561,RMVar_hsa_circ_119004,RMVar_hsa_circ_129075,RMVar_hsa_circ_129076,RMVar_hsa_circ_129077,RMVar_hsa_circ_327456,RMVar_hsa_circ_121812,RMVar_hsa_circ_54709,RMVar_hsa_circ_123133,RMVar_hsa_circ_129079,RMVar_hsa_circ_129080,RMVar_hsa_circ_89666,RMVar_hsa_circ_106703,RMVar_hsa_circ_129081,RMVar_hsa_circ_129082,RMVar_hsa_circ_129083,RMVar_hsa_circ_122585,RMVar_hsa_circ_129084,RMVar_hsa_circ_2864,RMVar_hsa_circ_84396,RMVar_hsa_circ_129085,RMVar_hsa_circ_129086 52257 RMVar_ID_52257 Human_SNP_ID_800873609 A-to-I Human chr1 + 26447747 26447747 26447747 ATGGCAGCTCACGCCTGTAATCCTAGCACATTAGGAGGCCGAGGTGGGCAGTCCACTTGAGGCAG ATGGCAGCTCACGCCTGTAATCCTAGCACATTGGGAGGCCGAGGTGGGCAGTCCACTTGAGGCAG A G DHDDS Ensembl:ENSG00000117682 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line chr1:26447746..26447747 23474544,29129909 RNA-Seq:(High) rs1249375587 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 7 haematopoietic and lymphoid tissue RMVar_hsa_circ_86519,RMVar_hsa_circ_103558,RMVar_hsa_circ_130652,RMVar_hsa_circ_130653,RMVar_hsa_circ_325134,RMVar_hsa_circ_122380,RMVar_hsa_circ_44987,RMVar_hsa_circ_130654,RMVar_hsa_circ_323750,RMVar_hsa_circ_299923,RMVar_hsa_circ_130655,RMVar_hsa_circ_301288,RMVar_hsa_circ_130661,RMVar_hsa_circ_130658,RMVar_hsa_circ_130659,RMVar_hsa_circ_289512,RMVar_hsa_circ_320907,RMVar_hsa_circ_130662 52258 RMVar_ID_52258 Human_SNP_ID_800877621 A-to-I Human chr1 + 31429510 31429510 31429510 GGTGGGATGCCCCGAGCATTGTGGGCCTCATCATCTTCCTCCTGTGCACCCTCTTCATCAGGTAT GGTGGGATGCCCCGAGCATTGTGGGCCTCATCGTCTTCCTCCTGTGCACCCTCTTCATCAGGTAT A G SERINC2 Ensembl:ENSG00000168528 Protein coding CDS GSE100210 HepG2 cell line chr1:31429509..31429510 29129909 RNA-Seq:(High) rs144747208 Functional Loss SNV COSMIC 33..33 33 rectum adenocarcinoma,large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_27397514 Human_Splice_Rec_40617,Human_Splice_Rec_40635,Human_Splice_Rec_40661,Human_Splice_Rec_40681,Human_Splice_Rec_40699 Human_miRNA_ID_3076179,Human_miRNA_ID_3076180,Human_miRNA_ID_3076181,Human_miRNA_ID_3076182 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_131077,RMVar_hsa_circ_122052,RMVar_hsa_circ_117413,RMVar_hsa_circ_131079,RMVar_hsa_circ_335345,RMVar_hsa_circ_43299,RMVar_hsa_circ_94979,RMVar_hsa_circ_126817,RMVar_hsa_circ_131080,RMVar_hsa_circ_131081,RMVar_hsa_circ_284457,RMVar_hsa_circ_131082,RMVar_hsa_circ_131083 52259 RMVar_ID_52259 Human_SNP_ID_800896771 A-to-I Human chr1 + 228180746 228180746 228180746 ACAGCTCACTACAGCCTCAACCTTCTGGGCTCAGATGATTCTCCTGCCTCAGCCTCCTGAGTAGC ACAGCTCACTACAGCCTCAACCTTCTGGGCTCCGATGATTCTCCTGCCTCAGCCTCCTGAGTAGC A C IBA57 Ensembl:ENSG00000181873 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line chr1:228180745..228180746 23474544,29129909 RNA-Seq:(High) rs1411542093 Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 2 breast 52260 RMVar_ID_52260 Human_SNP_ID_800897535 A-to-I Human chr1 + 155309905 155309905 155309905 TTCCCTACGGCGGCCCTCCCTGGTGCACGGGTACCCAGTCCTGGCCTGGCACAGTGCCCGCTGCT TTCCCTACGGCGGCCCTCCCTGGTGCACGGGTGCCCAGTCCTGGCCTGGCACAGTGCCCGCTGCT A G FDPS Ensembl:ENSG00000160752 Protein coding intron GSE100210 HepG2 cell line chr1:155309904..155309905 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 6 large intestine Human_RBP_ID_5335948 Human_Splice_Rec_138505,Human_Splice_Rec_138569,Human_Splice_Rec_138583,Human_Splice_Rec_138603 RMVar_hsa_circ_83643,RMVar_hsa_circ_99858,RMVar_hsa_circ_136559,RMVar_hsa_circ_136560 52261 RMVar_ID_52261 Human_SNP_ID_800900781 A-to-I Human chr1 - 229464696 229464696 229464696 ATGTTTCTCAGCTTAAGTCTGTGGATAAATCCAGTAATCGGGAAAGATATGACAATCTGGAGATG ATGTTTCTCAGCTTAAGTCTGTGGATAAATCCGGTAATCGGGAAAGATATGACAATCTGGAGATG T C NUP133 Ensembl:ENSG00000069248 Protein coding CDS GSE100210 HepG2 cell line chr1:229464695..229464696 29129909 RNA-Seq:(High) rs755831030 Functional Loss SNV COSMIC 33..33 33 mouth squamous_cell_carcinoma 1 head and neck Human_RBP_ID_1739478,Human_RBP_ID_8744778,Human_RBP_ID_9268039,Human_RBP_ID_9359933,Human_RBP_ID_26856104,Human_RBP_ID_27589229 Human_Splice_Rec_197277 RMVar_hsa_circ_35089,RMVar_hsa_circ_81578,RMVar_hsa_circ_91523,RMVar_hsa_circ_95693,RMVar_hsa_circ_24928,RMVar_hsa_circ_323393,RMVar_hsa_circ_140259,RMVar_hsa_circ_140260,RMVar_hsa_circ_140261,RMVar_hsa_circ_306068,RMVar_hsa_circ_48105,RMVar_hsa_circ_140268,RMVar_hsa_circ_140266,RMVar_hsa_circ_291230,RMVar_hsa_circ_118325,RMVar_hsa_circ_306351,RMVar_hsa_circ_73674,RMVar_hsa_circ_140269,RMVar_hsa_circ_140270,RMVar_hsa_circ_325677,RMVar_hsa_circ_54080,RMVar_hsa_circ_110361,RMVar_hsa_circ_292340,RMVar_hsa_circ_367218,RMVar_hsa_circ_140272,RMVar_hsa_circ_331935,RMVar_hsa_circ_297026,RMVar_hsa_circ_44670,RMVar_hsa_circ_66606,RMVar_hsa_circ_39969,RMVar_hsa_circ_99295,RMVar_hsa_circ_26722,RMVar_hsa_circ_140273,RMVar_hsa_circ_140275,RMVar_hsa_circ_140276,RMVar_hsa_circ_140274,RMVar_hsa_circ_285651,RMVar_hsa_circ_362050,RMVar_hsa_circ_298679,RMVar_hsa_circ_292588,RMVar_hsa_circ_36094,RMVar_hsa_circ_352201,RMVar_hsa_circ_140281,RMVar_hsa_circ_140282,RMVar_hsa_circ_366436,RMVar_hsa_circ_376218,RMVar_hsa_circ_290344,RMVar_hsa_circ_316061,RMVar_hsa_circ_125731,RMVar_hsa_circ_103300,RMVar_hsa_circ_114214,RMVar_hsa_circ_100760,RMVar_hsa_circ_77689,RMVar_hsa_circ_140284,RMVar_hsa_circ_140288,RMVar_hsa_circ_140290,RMVar_hsa_circ_97505,RMVar_hsa_circ_140291,RMVar_hsa_circ_140289,RMVar_hsa_circ_140286,RMVar_hsa_circ_140287,RMVar_hsa_circ_140285,RMVar_hsa_circ_94892,RMVar_hsa_circ_140283,RMVar_hsa_circ_352806,RMVar_hsa_circ_374880,RMVar_hsa_circ_291264,RMVar_hsa_circ_91370,RMVar_hsa_circ_140295,RMVar_hsa_circ_140297,RMVar_hsa_circ_22321,RMVar_hsa_circ_140298,RMVar_hsa_circ_140296,RMVar_hsa_circ_140294 52262 RMVar_ID_52262 Human_SNP_ID_800904705 A-to-I Human chr1 + 69919642 69919642 69919642 CTGATCAGCGGCTACATCCAGAAGATCAAGGCAGGAGAGAAGGACTTTGAGTCTCCGGCCTCACA CTGATCAGCGGCTACATCCAGAAGATCAAGGCGGGAGAGAAGGACTTTGAGTCTCCGGCCTCACA A G LRRC7,PIN1P1 Ensembl:ENSG00000033122,Ensembl:ENSG00000229359 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line chr1:69919641..69919642 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 5 head and neck RMVar_hsa_circ_9687,RMVar_hsa_circ_1540,RMVar_hsa_circ_19689,RMVar_hsa_circ_6001,RMVar_hsa_circ_336261,RMVar_hsa_circ_363740,RMVar_hsa_circ_336708,RMVar_hsa_circ_342608,RMVar_hsa_circ_344004,RMVar_hsa_circ_285037 52263 RMVar_ID_52263 Human_SNP_ID_800908585 A-to-I Human chr1 - 224312885 224312885 224312885 ATTCATATAAAGCTTTCTACCTAAAAAAAAAAAAAAATTATTTAAATAAGAAAAGGGCTTTTTTT ATTCATATAAAGCTTTCTACCTAAAAAAAAAAGAAAATTATTTAAATAAGAAAAGGGCTTTTTTT T C NVL Ensembl:ENSG00000143748 Protein coding intron GSE47997 K562 cells&HepG2 cells chr1:224312884..224312885 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_58648,RMVar_hsa_circ_73989,RMVar_hsa_circ_4043,RMVar_hsa_circ_98839,RMVar_hsa_circ_139862,RMVar_hsa_circ_50721,RMVar_hsa_circ_71691,RMVar_hsa_circ_60869,RMVar_hsa_circ_88659,RMVar_hsa_circ_139868,RMVar_hsa_circ_74461,RMVar_hsa_circ_69288,RMVar_hsa_circ_337789,RMVar_hsa_circ_378893,RMVar_hsa_circ_139871,RMVar_hsa_circ_60607 52264 RMVar_ID_52264 Human_SNP_ID_800953753 A-to-I Human chr1 - 233057763 233057763 233057763 CTCGGCCTCCTGGATTCAAGTTCAGCCTCCCAAGTAGCTGAGATTATAGGAGTGTGCCACCACAC CTCGGCCTCCTGGATTCAAGTTCAGCCTCCCACGTAGCTGAGATTATAGGAGTGTGCCACCACAC T G PCNX2 Ensembl:ENSG00000135749 Protein coding intron GSE47997;GSE100210;GSE107867 K562 cells&HepG2 cells;HepG2 cell line;ASD brains,cerebellum chr1:233057762..233057763 23474544,29129909,30559470 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 3 oesophagus RMVar_hsa_circ_2219,RMVar_hsa_circ_75934,RMVar_hsa_circ_80113,RMVar_hsa_circ_85264,RMVar_hsa_circ_140487,RMVar_hsa_circ_370343,RMVar_hsa_circ_117173,RMVar_hsa_circ_140490,RMVar_hsa_circ_140491,RMVar_hsa_circ_91439,RMVar_hsa_circ_113594,RMVar_hsa_circ_140493,RMVar_hsa_circ_140495,RMVar_hsa_circ_81895,RMVar_hsa_circ_140494,RMVar_hsa_circ_140492,RMVar_hsa_circ_324199,RMVar_hsa_circ_378777,RMVar_hsa_circ_140496,RMVar_hsa_circ_140502,RMVar_hsa_circ_96071,RMVar_hsa_circ_97696,RMVar_hsa_circ_76957,RMVar_hsa_circ_105697,RMVar_hsa_circ_140504,RMVar_hsa_circ_140505,RMVar_hsa_circ_140503,RMVar_hsa_circ_267179,RMVar_hsa_circ_26396,RMVar_hsa_circ_140508,RMVar_hsa_circ_12377,RMVar_hsa_circ_321569,RMVar_hsa_circ_365762,RMVar_hsa_circ_374338,RMVar_hsa_circ_374339,RMVar_hsa_circ_321736,RMVar_hsa_circ_301125,RMVar_hsa_circ_275025,RMVar_hsa_circ_52052,RMVar_hsa_circ_59902,RMVar_hsa_circ_24513,RMVar_hsa_circ_140518,RMVar_hsa_circ_140511,RMVar_hsa_circ_140513,RMVar_hsa_circ_140514,RMVar_hsa_circ_140512,RMVar_hsa_circ_119558,RMVar_hsa_circ_140510,RMVar_hsa_circ_76435,RMVar_hsa_circ_140517 52265 RMVar_ID_52265 Human_SNP_ID_800969304 A-to-I Human chr1 + 224938009 224938009 224938009 TAGGAAAGCTGGATAACTCTATGCAGAATAATAAAACTGGACCCCTATCTCTCACCATACACAAA TAGGAAAGCTGGATAACTCTATGCAGAATAATGAAACTGGACCCCTATCTCTCACCATACACAAA A G DNAH14 Ensembl:ENSG00000185842 Protein coding intron GSE100210 HepG2 cell line chr1:224938008..224938009 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ORCA 1 - Human_RBP_ID_19027974,Human_RBP_ID_22520489 52266 RMVar_ID_52266 Human_SNP_ID_800972333 A-to-I Human chr1 - 214390997 214390997 214390997 CCCCCCATCAGACGCCAGCCCACCTGGAGCCGATCCTCTCTGGTATGTATAGAAGCTGCAGTGAT CCCCCCATCAGACGCCAGCCCACCTGGAGCCGGTCCTCTCTGGTATGTATAGAAGCTGCAGTGAT T C PTPN14 Ensembl:ENSG00000152104 Protein coding CDS GSE38233 cultured B-cells chr1:214390996..214390997 24183664 RNA-Seq:(High) 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 52267 RMVar_ID_52267 Human_SNP_ID_800972622 A-to-I Human chr1 - 156322747 156322747 156322747 TCAAGCAGTTTTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTATAGGCATGTGCCACTACGCCTG TCAAGCAGTTTTCCTGCCTCAGCCTCCCGAGTTGCTGGGATTATAGGCATGTGCCACTACGCCTG T A CCT3 Ensembl:ENSG00000163468 Protein coding intron GSE38233 cultured B-cells chr1:156322746..156322747 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 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_136824 52268 RMVar_ID_52268 Human_SNP_ID_800973683 A-to-I Human chr1 - 15572484 15572484 15572484 GTGGTGGCGCGTGCCTATAGTCCCAGCTACTCAGGAAGCTGAGGCAGGGGCATTGCTTGAACCCG GTGGTGGCGCGTGCCTATAGTCCCAGCTACTCGGGAAGCTGAGGCAGGGGCATTGCTTGAACCCG T C AGMAT Ensembl:ENSG00000116771 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells chr1:15572483..15572484 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 52269 RMVar_ID_52269 Human_SNP_ID_800990089 A-to-I Human chr1 + 630560 630560 630560 ATCTACTCCACCTCAATCACACTACTCCCTATATCTAACAACGTAAAAATAAAATGACAGTTTGA ATCTACTCCACCTCAATCACACTACTCCCTATGTCTAACAACGTAAAAATAAAATGACAGTTTGA A G MTND2P28 Ensembl:ENSG00000225630 Pseudogene exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr1:630559..630560 30559470 RNA-Seq:(High) rs561754958 Functional Loss SNV ICGC 33..33 33 BRCA 1 - Human_RBP_ID_8240924,Human_RBP_ID_8315248,Human_RBP_ID_17182054,Human_RBP_ID_18509550,Human_RBP_ID_18523873 52270 RMVar_ID_52270 Human_SNP_ID_801019473 A-to-I Human chr1 - 219969945 219969945 219969945 TGGTGGCACACGCCTGTAATTCCAGCTACACTAGGAGGCTGGGGCACGAGAATTGCTTGAACCCA TGGTGGCACACGCCTGTAATTCCAGCTACACTGGGAGGCTGGGGCACGAGAATTGCTTGAACCCA T C EPRS1 Ensembl:ENSG00000136628 Protein coding intron GSE100210 HepG2 cell line chr1:219969944..219969945 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 2 breast Human_RBP_ID_10777586 RMVar_hsa_circ_139641,RMVar_hsa_circ_78102,RMVar_hsa_circ_83605,RMVar_hsa_circ_126425,RMVar_hsa_circ_139642,RMVar_hsa_circ_139643,RMVar_hsa_circ_139644,RMVar_hsa_circ_105348 52271 RMVar_ID_52271 Human_SNP_ID_801032890 A-to-I Human chr1 + 154227348 154227348 154227348 TTTCGGACCATAATGATGCTGACTTTGAGGAGAAGGTGAAACAAGTGAGTGTATCACTAATTTAC TTTCGGACCATAATGATGCTGACTTTGAGGAGGAGGTGAAACAAGTGAGTGTATCACTAATTTAC A G UBAP2L Ensembl:ENSG00000143569 Protein coding CDS GSE100210 HepG2 cell line chr1:154227348..154227349 29129909 RNA-Seq:(High) rs1368936617 Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_327340,Human_RBP_ID_1412404,Human_RBP_ID_1726088,Human_RBP_ID_5693037,Human_RBP_ID_10590555,Human_RBP_ID_18966006,Human_RBP_ID_23334134,Human_RBP_ID_27798564 Human_Splice_Rec_133880,Human_Splice_Rec_133881,Human_Splice_Rec_133926,Human_Splice_Rec_133927,Human_Splice_Rec_133972,Human_Splice_Rec_133973,Human_Splice_Rec_134022,Human_Splice_Rec_134023,Human_Splice_Rec_134032,Human_Splice_Rec_134033,Human_Splice_Rec_134050,Human_Splice_Rec_134051,Human_Splice_Rec_134068,Human_Splice_Rec_134069,Human_Splice_Rec_134118,Human_Splice_Rec_134119,Human_Splice_Rec_134136,Human_Splice_Rec_134137,Human_Splice_Rec_134148,Human_Splice_Rec_134149 RMVar_hsa_circ_106772,RMVar_hsa_circ_282860,RMVar_hsa_circ_115896,RMVar_hsa_circ_121210,RMVar_hsa_circ_136366,RMVar_hsa_circ_333997,RMVar_hsa_circ_350611,RMVar_hsa_circ_359817,RMVar_hsa_circ_136367,RMVar_hsa_circ_356443,RMVar_hsa_circ_340127,RMVar_hsa_circ_317384,RMVar_hsa_circ_333460,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_136372,RMVar_hsa_circ_136369,RMVar_hsa_circ_268210,RMVar_hsa_circ_301215,RMVar_hsa_circ_335129,RMVar_hsa_circ_287167,RMVar_hsa_circ_123093,RMVar_hsa_circ_136374,RMVar_hsa_circ_60689,RMVar_hsa_circ_136375,RMVar_hsa_circ_136373 52272 RMVar_ID_52272 Human_SNP_ID_801072004 A-to-I Human chr1 - 219970701 219970701 219970701 TGATCTCGGCTCACTGCAACCTCTGCCTCCCGAGTTCAAGCGATTCTCCTGCCTCAGCCTTCCAC TGATCTCGGCTCACTGCAACCTCTGCCTCCCGCGTTCAAGCGATTCTCCTGCCTCAGCCTTCCAC T G EPRS1 Ensembl:ENSG00000136628 Protein coding intron GSE38233 cultured B-cells chr1:219970700..219970701 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_139641,RMVar_hsa_circ_78102,RMVar_hsa_circ_83605,RMVar_hsa_circ_126425,RMVar_hsa_circ_139642,RMVar_hsa_circ_139643,RMVar_hsa_circ_139644,RMVar_hsa_circ_105348 52273 RMVar_ID_52273 Human_SNP_ID_801077861 A-to-I Human chr1 - 1801152 1801152 1801152 ATGGTGGCATGCGCTTGTAGTCCCAGCTGCTCAGGAGGCTGAAGCAGGAGAATTACTTGAACTGA ATGGTGGCATGCGCTTGTAGTCCCAGCTGCTCTGGAGGCTGAAGCAGGAGAATTACTTGAACTGA T A GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells chr1:1801151..1801152 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_128407,RMVar_hsa_circ_41253,RMVar_hsa_circ_92329,RMVar_hsa_circ_122805,RMVar_hsa_circ_127530,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_128389,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_109841,RMVar_hsa_circ_306773,RMVar_hsa_circ_342234,RMVar_hsa_circ_89721,RMVar_hsa_circ_128403,RMVar_hsa_circ_128405,RMVar_hsa_circ_3112,RMVar_hsa_circ_128404,RMVar_hsa_circ_128402,RMVar_hsa_circ_100327,RMVar_hsa_circ_373327,RMVar_hsa_circ_375577,RMVar_hsa_circ_324378,RMVar_hsa_circ_128408,RMVar_hsa_circ_128412,RMVar_hsa_circ_281145,RMVar_hsa_circ_317907,RMVar_hsa_circ_128406,RMVar_hsa_circ_376927,RMVar_hsa_circ_285895,RMVar_hsa_circ_128414,RMVar_hsa_circ_278200,RMVar_hsa_circ_128413,RMVar_hsa_circ_128411 52274 RMVar_ID_52274 Human_SNP_ID_801088750 A-to-I Human chr1 + 207360222 207360222 207360222 TGAAAGACTGAATCTTCCTTTGTTGCACAAATAGAGTTTGGAAAAAGCCTGTGAAAGGTGTCTTC TGAAAGACTGAATCTTCCTTTGTTGCACAAATGGAGTTTGGAAAAAGCCTGTGAAAGGTGTCTTC A G CD55 Ensembl:ENSG00000196352 Protein coding 3'UTR GSE100210 HepG2 cell line chr1:207360221..207360222 29129909 RNA-Seq:(High) rs1467997572 Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_339576,Human_RBP_ID_2118486,Human_RBP_ID_8296422,Human_RBP_ID_17181313,Human_RBP_ID_17580712,Human_RBP_ID_23206271,Human_RBP_ID_23359198,Human_RBP_ID_26374938 RMVar_hsa_circ_94382,RMVar_hsa_circ_139296 52275 RMVar_ID_52275 Human_SNP_ID_801089639 A-to-I Human chr1 - 243544513 243544513 243544513 CCCCAGGCTCAAGTATCCTCTCACCTCAGCCTACCAAGTAGCTCGGACTGCAGGCATGAGCCACC CCCCAGGCTCAAGTATCCTCTCACCTCAGCCTCCCAAGTAGCTCGGACTGCAGGCATGAGCCACC T G AKT3 Ensembl:ENSG00000117020 Protein coding intron GSE107867 ASD brains,cerebellum chr1:243544512..243544513 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_10874873 RMVar_hsa_circ_49893,RMVar_hsa_circ_141174,RMVar_hsa_circ_285344,RMVar_hsa_circ_295918,RMVar_hsa_circ_340959,RMVar_hsa_circ_276750,RMVar_hsa_circ_141177,RMVar_hsa_circ_141178 52276 RMVar_ID_52276 Human_SNP_ID_801126934 A-to-I Human chr1 - 61715482 61715482 61715482 CACCATGCCTGGCTAATTTGTGTATTTTTAGTAGAGACGGGGTTTTACCATGTTGGCCAGGCTGG CACCATGCCTGGCTAATTTGTGTATTTTTAGTGGAGACGGGGTTTTACCATGTTGGCCAGGCTGG T C TM2D1 Ensembl:ENSG00000162604 Protein coding intron GSE100210 HepG2 cell line chr1:61715481..61715482 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 prostate adenocarcinoma,PRAD 5 prostate RMVar_hsa_circ_37450,RMVar_hsa_circ_353610,RMVar_hsa_circ_133428,RMVar_hsa_circ_109298,RMVar_hsa_circ_342379,RMVar_hsa_circ_133429,RMVar_hsa_circ_133431,RMVar_hsa_circ_304829 52277 RMVar_ID_52277 Human_SNP_ID_801174929 A-to-I Human chr1 - 64841281 64841281 64841281 CCAGCAACTGAAGTGGACCCCACACATTTTGAAAAGCGCTTCCTAAAGAGGATCCGTGACTTGGG CCAGCAACTGAAGTGGACCCCACACATTTTGACAAGCGCTTCCTAAAGAGGATCCGTGACTTGGG T G JAK1 Ensembl:ENSG00000162434 Protein coding CDS GSE100210 HepG2 cell line chr1:64841280..64841281 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 3 liver Human_RBP_ID_26311362 Human_Splice_Rec_81738,Human_Splice_Rec_81739,Human_Splice_Rec_81784,Human_Splice_Rec_81785,Human_Splice_Rec_81832,Human_Splice_Rec_81833,Human_Splice_Rec_81882,Human_Splice_Rec_81883,Human_Splice_Rec_81904,Human_Splice_Rec_81905,Human_Splice_Rec_81952,Human_Splice_Rec_81953,Human_Splice_Rec_81990,Human_Splice_Rec_81991,Human_Splice_Rec_82034,Human_Splice_Rec_82035,Human_Splice_Rec_82080,Human_Splice_Rec_82081,Human_Splice_Rec_82128,Human_Splice_Rec_82129,Human_Splice_Rec_82174,Human_Splice_Rec_82175,Human_Splice_Rec_82218,Human_Splice_Rec_82219,Human_Splice_Rec_82264,Human_Splice_Rec_82265,Human_Splice_Rec_82288,Human_Splice_Rec_82289,Human_Splice_Rec_82301 RMVar_hsa_circ_78715,RMVar_hsa_circ_114164,RMVar_hsa_circ_117983,RMVar_hsa_circ_133661,RMVar_hsa_circ_123711,RMVar_hsa_circ_133663,RMVar_hsa_circ_133664,RMVar_hsa_circ_109212,RMVar_hsa_circ_133665,RMVar_hsa_circ_76808,RMVar_hsa_circ_133666,RMVar_hsa_circ_265520,RMVar_hsa_circ_133667 52278 RMVar_ID_52278 Human_SNP_ID_801184754 A-to-I Human chr1 - 149887690 149887687 149887690 GCTGGCGGGCAACGCGGCTCGGGACAACAAGAAGACGCGCATCATCCCTCGCCATCTGCAACTAG GCTGGCGGGCAACGCGGCTCGGGACAACAAGA___CGCGCATCATCCCTCGCCATCTGCAACTAG GTCT G H2AC21 Ensembl:ENSG00000184270 Protein coding CDS GSE100210 HepG2 cell line chr1:149887689..149887690 29129909 RNA-Seq:(High) rs782564731 Functional Loss DEL TCGA,ICGC 33..35 33 COCA,UCEC 2 - Human_RBP_ID_3990990,Human_RBP_ID_26389721,Human_RBP_ID_27387518 52279 RMVar_ID_52279 Human_SNP_ID_801214809 A-to-I Human chr1 - 247100415 247100415 247100415 ATATAGAGGCTGGGTGTAGTGACTCAGCCTATAATCCCAGCACTTTGGGAGGCCAAGGCGTGTGG ATATAGAGGCTGGGTGTAGTGACTCAGCCTATGATCCCAGCACTTTGGGAGGCCAAGGCGTGTGG T C ZNF669 Ensembl:ENSG00000188295 Protein coding CDS GSE56152 embryonic stem cells,wild type chr1:247100414..247100415 25708366 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 bile_duct adenocarcinoma,biliary_tract adenocarcinoma,colon adenocarcinoma,large_intestine adenocarcinoma 6 biliary tract,gallbladder,large intestine Human_RBP_ID_17746608 52280 RMVar_ID_52280 Human_SNP_ID_801218717 A-to-I Human chr1 - 243834026 243834026 243834026 CCAGCTATCAAATTAGAATCCTGTACAATTTAAAAAATCCTTCAAAATGAAGATGAGCCCAGCCA CCAGCTATCAAATTAGAATCCTGTACAATTTATAAAATCCTTCAAAATGAAGATGAGCCCAGCCA T A AKT3 Ensembl:ENSG00000117020 Protein coding intron GSE107867 ASD brains,frontal_cortex chr1:243834025..243834026 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_276750,RMVar_hsa_circ_269994,RMVar_hsa_circ_141184,RMVar_hsa_circ_270555,RMVar_hsa_circ_141194,RMVar_hsa_circ_271040,RMVar_hsa_circ_307063,RMVar_hsa_circ_141195,RMVar_hsa_circ_271937,RMVar_hsa_circ_141207,RMVar_hsa_circ_5181,RMVar_hsa_circ_272058,RMVar_hsa_circ_141210,RMVar_hsa_circ_304502,RMVar_hsa_circ_141216,RMVar_hsa_circ_274361,RMVar_hsa_circ_299777,RMVar_hsa_circ_141224 52281 RMVar_ID_52281 Human_SNP_ID_801223207 A-to-I Human chr1 + 32553629 32553629 32553629 AATTCTGGGGCCGGGCGCGGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGTCAAGGCAGAC AATTCTGGGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGTCAAGGCAGAC A G ZBTB8A,AL033529.1 Ensembl:ENSG00000160062,Ensembl:ENSG00000254553 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line chr1:32553628..32553629 29129909 RNA-Seq:(High) rs1001506869 Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 3 oesophagus RMVar_hsa_circ_103986,RMVar_hsa_circ_114995,RMVar_hsa_circ_131250,RMVar_hsa_circ_131251,RMVar_hsa_circ_116159,RMVar_hsa_circ_118785,RMVar_hsa_circ_131253,RMVar_hsa_circ_131256,RMVar_hsa_circ_131258,RMVar_hsa_circ_332692,RMVar_hsa_circ_131255,RMVar_hsa_circ_309677,RMVar_hsa_circ_131257 52282 RMVar_ID_52282 Human_SNP_ID_801241872 A-to-I Human chr1 + 14821386 14821385 14821386 AAATACAAAACAAATTAGCCAGGTGTTGTGGCAGGCACCTGTAATCCCAGCTACTTGGGAGGCTG AAATACAAAACAAATTAGCCAGGTGTTGTGGC_GGCACCTGTAATCCCAGCTACTTGGGAGGCTG CA C KAZN Ensembl:ENSG00000189337 Protein coding intron GSE47997 K562 cells&HepG2 cells chr1:14821385..14821386 23474544 RNA-Seq:(High) rs754970377 Functional Loss DEL ICGC 33..33 33 LMS 1 - 52283 RMVar_ID_52283 Human_SNP_ID_801273933 A-to-I Human chr1 + 32669922 32669922 32669922 CAAAAAAAAAGAAAAAAGAAAAACCTGGATGTATGAGTGGGCACACATGTGCTTTATGCCGTTGC CAAAAAAAAAGAAAAAAGAAAAACCTGGATGTGTGAGTGGGCACACATGTGCTTTATGCCGTTGC A G RBBP4 Ensembl:ENSG00000162521 Protein coding intron GSE38233 cultured B-cells chr1:32669921..32669922 24183664 RNA-Seq:(High) rs359957 Functional Loss SNV ICGC 33..33 33 COCA 1 - GWAS_ID_3487,GWAS_ID_3488,GWAS_ID_3489 RMVar_hsa_circ_5036,RMVar_hsa_circ_309059,RMVar_hsa_circ_322338,RMVar_hsa_circ_59103,RMVar_hsa_circ_131276,RMVar_hsa_circ_279080,RMVar_hsa_circ_10286,RMVar_hsa_circ_27413,RMVar_hsa_circ_128206,RMVar_hsa_circ_323087,RMVar_hsa_circ_131280 52284 RMVar_ID_52284 Human_SNP_ID_801276699 A-to-I Human chr1 - 150600814 150600814 150600814 TGGCTCAATGCAACCTCTGCCTCCCGGATTCAAGCGATTCTTCTGCCTCAGCCTCTGAGTAGCTG TGGCTCAATGCAACCTCTGCCTCCCGGATTCAGGCGATTCTTCTGCCTCAGCCTCTGAGTAGCTG T C RF00017-1784 RNACentral:URS0000904F64 SRP RNA intron GSE100210 HepG2 cell line chr1:150600813..150600814 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 52285 RMVar_ID_52285 Human_SNP_ID_801281595 A-to-I Human chr1 + 168244197 168244197 168244197 CTCTGACTGGTTTTTTTTTTTTTTTCTTTTTGAGATGGAGTCTCACTCCGTCGCCCAGGCTGGAG CTCTGACTGGTTTTTTTTTTTTTTTCTTTTTGTGATGGAGTCTCACTCCGTCGCCCAGGCTGGAG A T SFT2D2 Ensembl:ENSG00000213064 Protein coding 3'UTR GSE100210 HepG2 cell line chr1:168244196..168244197 29129909 RNA-Seq:(High) rs1385044164 Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_5709592,Human_RBP_ID_11188142,Human_RBP_ID_19445967,Human_RBP_ID_24395722,Human_RBP_ID_24448193 52286 RMVar_ID_52286 Human_SNP_ID_801283689 A-to-I Human chr1 - 77705247 77705247 77705247 GAGATTGCAGTGAGCCGAGATCGCACCACTGCACTCCAGCCTGGATGAAAGAGTGAGATTCTGTC GAGATTGCAGTGAGCCGAGATCGCACCACTGCCCTCCAGCCTGGATGAAAGAGTGAGATTCTGTC T G USP33 Ensembl:ENSG00000077254 Protein coding intron GSE100210 HepG2 cell line chr1:77705246..77705247 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 4 ovary RMVar_hsa_circ_41163,RMVar_hsa_circ_115321,RMVar_hsa_circ_134072,RMVar_hsa_circ_333613,RMVar_hsa_circ_18664,RMVar_hsa_circ_299131,RMVar_hsa_circ_134074,RMVar_hsa_circ_9107,RMVar_hsa_circ_299345,RMVar_hsa_circ_305980,RMVar_hsa_circ_39034,RMVar_hsa_circ_290819,RMVar_hsa_circ_36160,RMVar_hsa_circ_134075,RMVar_hsa_circ_134077,RMVar_hsa_circ_134078,RMVar_hsa_circ_134076 52287 RMVar_ID_52287 Human_SNP_ID_801330085 A-to-I Human chr1 - 31908228 31908228 31908228 TTTTAGATAAAAAAAAAAAAAAAACAAAAAACAACACCAAAAAAACAGCAGTGATATATATATAT TTTTAGATAAAAAAAAAAAAAAAACAAAAAACTACACCAAAAAAACAGCAGTGATATATATATAT T A AL136115.2,PTP4A2 Ensembl:ENSG00000269967,Ensembl:ENSG00000184007 lincRNA,Protein coding intron,3'UTR GSE38233 cultured B-cells chr1:31908228..31908229 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_352097,Human_RBP_ID_18174795 RMVar_hsa_circ_92456,RMVar_hsa_circ_112601,RMVar_hsa_circ_122320,RMVar_hsa_circ_103168,RMVar_hsa_circ_131129,RMVar_hsa_circ_131131,RMVar_hsa_circ_131132,RMVar_hsa_circ_131130,RMVar_hsa_circ_131133 52288 RMVar_ID_52288 Human_SNP_ID_801335104 A-to-I Human chr1 - 160332454 160332454 160332454 CCAGCCTGGACCAGACTGTGCGCGTTTGGGATATTTCTGGTGAGCTGCCCAAGTTCAGAGGACAA CCAGCCTGGACCAGACTGTGCGCGTTTGGGATGTTTCTGGTGAGCTGCCCAAGTTCAGAGGACAA T C COPA Ensembl:ENSG00000122218 Protein coding CDS GSE56152;GSE100210 embryonic stem cells,wild type;HepG2 cell line chr1:160332453..160332454 25708366,29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 rectum adenocarcinoma,large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_17764919,Human_RBP_ID_18969249,Human_RBP_ID_19035645,Human_RBP_ID_23338118 Human_Splice_Rec_147551,Human_Splice_Rec_147613,Human_Splice_Rec_147667,Human_Splice_Rec_147729,Human_Splice_Rec_147791,Human_Splice_Rec_147849,Human_Splice_Rec_147913,Human_Splice_Rec_147975,Human_Splice_Rec_148037,Human_Splice_Rec_148123,Human_Splice_Rec_148187,Human_Splice_Rec_148237,Human_Splice_Rec_148301 RMVar_hsa_circ_99830,RMVar_hsa_circ_137018,RMVar_hsa_circ_4835,RMVar_hsa_circ_109880,RMVar_hsa_circ_137027,RMVar_hsa_circ_137028,RMVar_hsa_circ_97323,RMVar_hsa_circ_86396,RMVar_hsa_circ_88577,RMVar_hsa_circ_137036,RMVar_hsa_circ_326348,RMVar_hsa_circ_137038,RMVar_hsa_circ_137039,RMVar_hsa_circ_329218,RMVar_hsa_circ_77953,RMVar_hsa_circ_137043,RMVar_hsa_circ_137042,RMVar_hsa_circ_119249,RMVar_hsa_circ_137049,RMVar_hsa_circ_372695,RMVar_hsa_circ_137053,RMVar_hsa_circ_121007,RMVar_hsa_circ_137052,RMVar_hsa_circ_353959,RMVar_hsa_circ_38219,RMVar_hsa_circ_81166,RMVar_hsa_circ_120443,RMVar_hsa_circ_126411,RMVar_hsa_circ_137056,RMVar_hsa_circ_45880,RMVar_hsa_circ_84740,RMVar_hsa_circ_137057,RMVar_hsa_circ_332104,RMVar_hsa_circ_137055,RMVar_hsa_circ_90612,RMVar_hsa_circ_137066,RMVar_hsa_circ_137067,RMVar_hsa_circ_137068,RMVar_hsa_circ_82993,RMVar_hsa_circ_137069,RMVar_hsa_circ_345145,RMVar_hsa_circ_137071,RMVar_hsa_circ_22108,RMVar_hsa_circ_93602,RMVar_hsa_circ_276933,RMVar_hsa_circ_137073,RMVar_hsa_circ_137072,RMVar_hsa_circ_297535,RMVar_hsa_circ_137076,RMVar_hsa_circ_372702,RMVar_hsa_circ_137075,RMVar_hsa_circ_374929,RMVar_hsa_circ_137077 52289 RMVar_ID_52289 Human_SNP_ID_801336998 A-to-I Human chr1 + 25346525 25346525 25346525 TTAAGCAGTCCTCTGGCCTCAGCCTCCCCAGTAGCTAGGACTACTTGCACATACCACCACACCCA TTAAGCAGTCCTCTGGCCTCAGCCTCCCCAGTGGCTAGGACTACTTGCACATACCACCACACCCA A G TMEM50A Ensembl:ENSG00000183726 Protein coding intron GSE38233 cultured B-cells chr1:25346524..25346525 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_99019,RMVar_hsa_circ_130553,RMVar_hsa_circ_270899,RMVar_hsa_circ_301031,RMVar_hsa_circ_296148,RMVar_hsa_circ_100049,RMVar_hsa_circ_130554,RMVar_hsa_circ_130555,RMVar_hsa_circ_130552,RMVar_hsa_circ_303047,RMVar_hsa_circ_130557,RMVar_hsa_circ_70829,RMVar_hsa_circ_130558 52290 RMVar_ID_52290 Human_SNP_ID_801347557 A-to-I Human chr1 + 32024327 32024327 32024327 GGTTTTCTAAAATTTTTTATTAATTTTTTTTTAGAGACAGGGTCTTGTTCTGTCACCCAAGCTGG GGTTTTCTAAAATTTTTTATTAATTTTTTTTTTGAGACAGGGTCTTGTTCTGTCACCCAAGCTGG A T KHDRBS1 Ensembl:ENSG00000121774 Protein coding intron GSE38233 cultured B-cells chr1:32024326..32024327 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 3 oesophagus Human_RBP_ID_5810546,Human_RBP_ID_10936670,Human_RBP_ID_17557090,Human_RBP_ID_24684099 52291 RMVar_ID_52291 Human_SNP_ID_801364848 A-to-I Human chr1 - 31263953 31263953 31263953 TCTATACTTTACCCTTTAATGACTTAAGCAAGATTGAGGGTCAAAGGAACTTTTTTTTTTTTTTT TCTATACTTTACCCTTTAATGACTTAAGCAAGGTTGAGGGTCAAAGGAACTTTTTTTTTTTTTTT T C SNRNP40 Ensembl:ENSG00000060688 Protein coding intron GSE38233 cultured B-cells chr1:31263952..31263953 24183664 RNA-Seq:(High) rs4949202 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_5809397 GWAS_ID_3446,GWAS_ID_3447,GWAS_ID_3448,GWAS_ID_3449,GWAS_ID_3450,GWAS_ID_3451,GWAS_ID_3452,GWAS_ID_3453,GWAS_ID_3454,GWAS_ID_3455,GWAS_ID_3456,GWAS_ID_3457,GWAS_ID_3458,GWAS_ID_3459,GWAS_ID_3460,GWAS_ID_3461,GWAS_ID_3462,GWAS_ID_3463,GWAS_ID_3464,GWAS_ID_3465,GWAS_ID_3466,GWAS_ID_3467,GWAS_ID_3468,GWAS_ID_3469,GWAS_ID_3470,GWAS_ID_3471,GWAS_ID_3472,GWAS_ID_3473,GWAS_ID_3474,GWAS_ID_3475,GWAS_ID_3476,GWAS_ID_3477,GWAS_ID_3478,GWAS_ID_3479,GWAS_ID_3480,GWAS_ID_3481,GWAS_ID_3482,GWAS_ID_3483,GWAS_ID_3484,GWAS_ID_3485,GWAS_ID_3486 RMVar_hsa_circ_1173,RMVar_hsa_circ_77241,RMVar_hsa_circ_38215,RMVar_hsa_circ_79760,RMVar_hsa_circ_131047,RMVar_hsa_circ_304438,RMVar_hsa_circ_50169,RMVar_hsa_circ_8040,RMVar_hsa_circ_131048,RMVar_hsa_circ_131049 52292 RMVar_ID_52292 Human_SNP_ID_801368929 A-to-I Human chr1 - 150621549 150621549 150621549 AAACTCCAGCGGGTGTACGGTGGCTCACGCCTATAATTCCAGCACTTTGGGAGGCCAAGGTGGGT AAACTCCAGCGGGTGTACGGTGGCTCACGCCTGTAATTCCAGCACTTTGGGAGGCCAAGGTGGGT T C ENSA Ensembl:ENSG00000143420 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line chr1:150621548..150621549 24183664,29129909,31158229 RNA-Seq:(High) rs1016829948 Functional Loss SNV ICGC 33..33 33 RECA 1 - 52293 RMVar_ID_52293 Human_SNP_ID_801423654 A-to-I Human chr1 - 155930344 155930344 155930344 TTATTGACTTTATTTAATGTCATTTTAGTGAGATTTTTGTTTGCTTGTTAATTCGTTTATGAAGA TTATTGACTTTATTTAATGTCATTTTAGTGAGGTTTTTGTTTGCTTGTTAATTCGTTTATGAAGA T C KHDC4 Ensembl:ENSG00000132680 Protein coding intron GSE38233 cultured B-cells chr1:155930343..155930344 24183664 RNA-Seq:(High) rs3768280 Functional Loss SNV COSMIC 33..33 33 central_nervous_system oligodendroglioma_Grade_III,frontal_lobe oligodendroglioma_Grade_III 3 brain Human_RBP_ID_10603786 GWAS_ID_4077,GWAS_ID_4078,GWAS_ID_4079,GWAS_ID_4080,GWAS_ID_4081,GWAS_ID_4082,GWAS_ID_4083,GWAS_ID_4084 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 52294 RMVar_ID_52294 Human_SNP_ID_801425817 A-to-I Human chr1 - 150618889 150618889 150618889 CAACTCACTGCAACCTCTGCCTCCTGGGTTCAAGCTATTCTCCTGCCTCAGCCACCTGAGTAGCT CAACTCACTGCAACCTCTGCCTCCTGGGTTCATGCTATTCTCCTGCCTCAGCCACCTGAGTAGCT T A ENSA Ensembl:ENSG00000143420 Protein coding intron GSE38233 cultured B-cells chr1:150618888..150618889 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 2 liver 52295 RMVar_ID_52295 Human_SNP_ID_801478257 A-to-I Human chr1 + 52074235 52074235 52074235 GTTTTTTGTTTTTTGAGATAGAGTCTCACTCTATGCCCAGGCTGGAGTGCAGTGGCACAGTCTTG GTTTTTTGTTTTTTGAGATAGAGTCTCACTCTGTGCCCAGGCTGGAGTGCAGTGGCACAGTCTTG A G BTF3L4 Ensembl:ENSG00000134717 Protein coding intron GSE38233 cultured B-cells chr1:52074234..52074235 24183664 RNA-Seq:(High) rs77641918 Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_122798,RMVar_hsa_circ_132924 52296 RMVar_ID_52296 Human_SNP_ID_801483229 A-to-I Human chr1 + 155566407 155566407 155566407 TAAATCCCAACACTTTGGGCGACTGAGGCAGGAGGATTACTTGAGGCCAGGAGTTCAAGACCAGC TAAATCCCAACACTTTGGGCGACTGAGGCAGGGGGATTACTTGAGGCCAGGAGTTCAAGACCAGC A G ASH1L-AS1,ASH1L-AS1:2,ASH1L-AS1:3 RNACentral:URS0000D5A569,RNACentral:URS0000D57E5C,RNACentral:URS0000D5E18C lincRNA,lincRNA,lincRNA exon,intron,exon GSE100210 HepG2 cell line chr1:155566406..155566407 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_10598851 52297 RMVar_ID_52297 Human_SNP_ID_801529640 A-to-I Human chr1 - 23874310 23874310 23874310 TGGATAGGTAGGGCCACGAGGAGTAGCCAGGTAGGCGAGACACAAAAGGCCTGGGACAGGGTCAG TGGATAGGTAGGGCCACGAGGAGTAGCCAGGTGGGCGAGACACAAAAGGCCTGGGACAGGGTCAG T C CNR2 Ensembl:ENSG00000188822 Protein coding 3'UTR GSE38233 cultured B-cells chr1:23874309..23874310 24183664 RNA-Seq:(High) rs1105 Functional Loss SNV ICGC 33..33 33 LUSC 1 - 52298 RMVar_ID_52298 Human_SNP_ID_801534300 A-to-I Human chr1 + 1607371 1607371 1607371 TCCTTTTTTTTTTTTTTTTTTTTGAGAGTCTCACTCTGTTGCCTAGACTGGAGTGCAATGGCGTG TCCTTTTTTTTTTTTTTTTTTTTGAGAGTCTCTCTCTGTTGCCTAGACTGGAGTGCAATGGCGTG A T LOC105378586 RNACentral:URS00008BC95F lincRNA exon GSE100210 HepG2 cell line chr1:1607370..1607371 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 52299 RMVar_ID_52299 Human_SNP_ID_801542300 A-to-I Human chr1 + 32845699 32845699 32845699 GATATGTTTTCATTTTCTTTTTTTTTTTTTTTAAGATAAAGCCTTGCTCTGTCACCCAGCCTGAG GATATGTTTTCATTTTCTTTTTTTTTTTTTTTTAGATAAAGCCTTGCTCTGTCACCCAGCCTGAG A T S100PBP Ensembl:ENSG00000116497 Protein coding intron GSE38233 cultured B-cells chr1:32845698..32845699 24183664 RNA-Seq:(High) rs1270114838 Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 3 pancreas Human_RBP_ID_5909065,Human_RBP_ID_10948415,Human_RBP_ID_23149115 RMVar_hsa_circ_90137,RMVar_hsa_circ_131305,RMVar_hsa_circ_273527,RMVar_hsa_circ_131307,RMVar_hsa_circ_17462 52300 RMVar_ID_52300 Human_SNP_ID_801547886 A-to-I Human chr1 - 222641792 222641792 222641792 TAGAAATGCTCAAGAACCAGCTGGACCAGGAAATGGAGTTCTTGTCCACCTCCATTGCCCAGCTC TAGAAATGCTCAAGAACCAGCTGGACCAGGAAGTGGAGTTCTTGTCCACCTCCATTGCCCAGCTC T C AL592148.1 Ensembl:ENSG00000229399 Pseudogene exon GSE100210 HepG2 cell line chr1:222641791..222641792 29129909 RNA-Seq:(High) rs878994747 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 haematopoietic and lymphoid tissue Human_RBP_ID_1421337,Human_RBP_ID_5155920,Human_RBP_ID_8299065,Human_RBP_ID_17340199,Human_RBP_ID_18563480,Human_RBP_ID_26375707 Human_miRNA_ID_1826677,Human_miRNA_ID_2046488 52301 RMVar_ID_52301 Human_SNP_ID_801558128 A-to-I Human chr1 + 22082034 22082034 22082034 GAACAGTGTAGTAGATGAAGTAGAGTGAGACTAGAGTGCATCATACAAGCTCCAAATTGAACTAA GAACAGTGTAGTAGATGAAGTAGAGTGAGACTGGAGTGCATCATACAAGCTCCAAATTGAACTAA A G CDC42 Ensembl:ENSG00000070831 Protein coding intron GSE38233 cultured B-cells chr1:22082033..22082034 24183664 RNA-Seq:(High) rs2056975 Functional Loss SNV ICGC 33..33 33 ESCA 1 - GWAS_ID_652,GWAS_ID_653,GWAS_ID_654,GWAS_ID_655,GWAS_ID_656,GWAS_ID_657,GWAS_ID_658,GWAS_ID_659,GWAS_ID_660,GWAS_ID_661,GWAS_ID_662,GWAS_ID_663,GWAS_ID_664,GWAS_ID_665,GWAS_ID_666,GWAS_ID_667,GWAS_ID_668,GWAS_ID_669,GWAS_ID_670,GWAS_ID_671,GWAS_ID_672,GWAS_ID_673,GWAS_ID_674,GWAS_ID_675,GWAS_ID_676,GWAS_ID_677,GWAS_ID_678,GWAS_ID_679,GWAS_ID_680,GWAS_ID_681,GWAS_ID_682,GWAS_ID_683,GWAS_ID_684 RMVar_hsa_circ_97695,RMVar_hsa_circ_103628,RMVar_hsa_circ_342544,RMVar_hsa_circ_130355,RMVar_hsa_circ_378086,RMVar_hsa_circ_345538,RMVar_hsa_circ_276873,RMVar_hsa_circ_100439,RMVar_hsa_circ_104993,RMVar_hsa_circ_130356,RMVar_hsa_circ_130357,RMVar_hsa_circ_130358,RMVar_hsa_circ_127635,RMVar_hsa_circ_130359,RMVar_hsa_circ_130360,RMVar_hsa_circ_130362 52302 RMVar_ID_52302 Human_SNP_ID_801563735 A-to-I Human chr1 - 163076307 163076307 163076307 CCTGCATCTTTAATACAGTGAGATTTGTATGCATACACTCTGGTGTCTTCATTTTGCAGCCCATT CCTGCATCTTTAATACAGTGAGATTTGTATGCGTACACTCTGGTGTCTTCATTTTGCAGCCCATT T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr1:163076307..163076308 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 52303 RMVar_ID_52303 Human_SNP_ID_801572010 A-to-I Human chr1 + 228115365 228115365 228115365 AGATAGTTCGAATCAAATCATAAACCTCTAGCACTTTCTCTTCCATGATCCGGGGCTGCCGGGCA AGATAGTTCGAATCAAATCATAAACCTCTAGCGCTTTCTCTTCCATGATCCGGGGCTGCCGGGCA A G lnc-ARF1-3,lnc-ARF1-3:2,lnc-ARF1-3:3 RNACentral:URS0000D5BE25,RNACentral:URS0000D5BE5E,RNACentral:URS00008C1AA8 lincRNA,lincRNA,lincRNA intron,exon,intron GSE100210 HepG2 cell line chr1:228115364..228115365 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 1 - 52304 RMVar_ID_52304 Human_SNP_ID_801608439 A-to-I Human chr1 - 1806817 1806817 1806817 GAGACGCACTACCATGCCCGGCTAATTTTTGTATTTTTAATAGAGACAGGGTTTCGCCATGCTGG GAGACGCACTACCATGCCCGGCTAATTTTTGTGTTTTTAATAGAGACAGGGTTTCGCCATGCTGG T C GNB1 Ensembl:ENSG00000078369 Protein coding intron GSE38233 cultured B-cells chr1:1806816..1806817 24183664 RNA-Seq:(High) rs916159789 Functional Loss SNV ICGC 33..33 33 COCA 1 - 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_3112,RMVar_hsa_circ_128404,RMVar_hsa_circ_100327,RMVar_hsa_circ_375577,RMVar_hsa_circ_324378,RMVar_hsa_circ_128416,RMVar_hsa_circ_83173,RMVar_hsa_circ_128412,RMVar_hsa_circ_281145,RMVar_hsa_circ_317907,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_300397,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_128422,RMVar_hsa_circ_293069,RMVar_hsa_circ_324871,RMVar_hsa_circ_273354,RMVar_hsa_circ_128426,RMVar_hsa_circ_128427,RMVar_hsa_circ_128424 52305 RMVar_ID_52305 Human_SNP_ID_801688518 A-to-I Human chr1 - 114415242 114415242 114415242 CTGTAGTCCCAGCACTTTGAGGAGGCCAAGATAGGAAGAGCACTTGAGGCCAGGAGTTCGAGACT CTGTAGTCCCAGCACTTTGAGGAGGCCAAGATCGGAAGAGCACTTGAGGCCAGGAGTTCGAGACT T G TRIM33 Ensembl:ENSG00000197323 Protein coding intron GSE47997 K562 cells&HepG2 cells chr1:114415241..114415242 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 COCA 1 - Human_RBP_ID_10533918,Human_RBP_ID_24750636 RMVar_hsa_circ_74288,RMVar_hsa_circ_135531,RMVar_hsa_circ_112335,RMVar_hsa_circ_135533,RMVar_hsa_circ_135535,RMVar_hsa_circ_75355,RMVar_hsa_circ_116113 52306 RMVar_ID_52306 Human_SNP_ID_801707046 A-to-I Human chr1 + 32225514 32225514 32225514 CCTGTAATCCCAGCACTTTGGGAGGTTGAGGCAGGTGGATCACCTGAGGTCAGGAGTGCAAGACC CCTGTAATCCCAGCACTTTGGGAGGTTGAGGCGGGTGGATCACCTGAGGTCAGGAGTGCAAGACC A G EIF3I Ensembl:ENSG00000084623 Protein coding intron GSE38233 cultured B-cells chr1:32225513..32225514 24183664 RNA-Seq:(High) rs1245828325 Functional Loss SNV ICGC 33..33 33 PRAD 2 - RMVar_hsa_circ_77506,RMVar_hsa_circ_5429,RMVar_hsa_circ_108103,RMVar_hsa_circ_131197,RMVar_hsa_circ_88535,RMVar_hsa_circ_84932,RMVar_hsa_circ_131199,RMVar_hsa_circ_299286,RMVar_hsa_circ_375854,RMVar_hsa_circ_109713,RMVar_hsa_circ_94282,RMVar_hsa_circ_131202,RMVar_hsa_circ_131204,RMVar_hsa_circ_131203,RMVar_hsa_circ_131200,RMVar_hsa_circ_131201,RMVar_hsa_circ_131208,RMVar_hsa_circ_131209 52307 RMVar_ID_52307 Human_SNP_ID_801742792 A-to-I Human chr1 - 21731459 21731459 21731459 AGGAGTTTGAGACCAGCCTGGCCAACGTGGTAAATCCTCATCTCCACTAAAAATGCAAAAATTAC AGGAGTTTGAGACCAGCCTGGCCAACGTGGTATATCCTCATCTCCACTAAAAATGCAAAAATTAC T A USP48 Ensembl:ENSG00000090686 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr1:21731458..21731459 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_61016,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_14842,RMVar_hsa_circ_130085,RMVar_hsa_circ_94140,RMVar_hsa_circ_269122,RMVar_hsa_circ_356564,RMVar_hsa_circ_378750,RMVar_hsa_circ_341188,RMVar_hsa_circ_47632,RMVar_hsa_circ_130087,RMVar_hsa_circ_345155,RMVar_hsa_circ_327037,RMVar_hsa_circ_275100,RMVar_hsa_circ_33068,RMVar_hsa_circ_266719,RMVar_hsa_circ_55095,RMVar_hsa_circ_88666,RMVar_hsa_circ_130095,RMVar_hsa_circ_70094,RMVar_hsa_circ_24423,RMVar_hsa_circ_130096,RMVar_hsa_circ_31546,RMVar_hsa_circ_47499,RMVar_hsa_circ_265895,RMVar_hsa_circ_11237 52308 RMVar_ID_52308 Human_SNP_ID_801755426 A-to-I Human chr1 - 149887662 149887662 149887662 AAGAAGACGCGCATCATCCCTCGCCATCTGCAACTAGCCGTGAGGAATGACGAAGAGCTCAACAA AAGAAGACGCGCATCATCCCTCGCCATCTGCATCTAGCCGTGAGGAATGACGAAGAGCTCAACAA T A H2AC21 Ensembl:ENSG00000184270 Protein coding CDS GSE100210 HepG2 cell line chr1:149887661..149887662 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_1411090,Human_RBP_ID_1724787,Human_RBP_ID_3990983,Human_RBP_ID_18550716 52309 RMVar_ID_52309 Human_SNP_ID_801763955 A-to-I Human chr1 - 26876344 26876344 26876344 GGGCATGGTGGCATGCGCCTGTAATTCCAGCTACTTAGGAGACTGAGGCAGGAGAATCGCTTGAA GGGCATGGTGGCATGCGCCTGTAATTCCAGCTGCTTAGGAGACTGAGGCAGGAGAATCGCTTGAA T C GPN2 Ensembl:ENSG00000142751 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr1:26876343..26876344 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 52310 RMVar_ID_52310 Human_SNP_ID_801768186 A-to-I Human chr1 - 155671283 155671283 155671283 GGAATTACAGGTGCGTGCCACCATGCCTGGCTAATTTTTACATTTTTGGTAGAGATGGGGTTTCA GGAATTACAGGTGCGTGCCACCATGCCTGGCTTATTTTTACATTTTTGGTAGAGATGGGGTTTCA T A YY1AP1 Ensembl:ENSG00000163374 Protein coding intron GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line chr1:155671282..155671283 23474544,24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 RECA 1 - RMVar_hsa_circ_6989,RMVar_hsa_circ_78938,RMVar_hsa_circ_26391,RMVar_hsa_circ_68465,RMVar_hsa_circ_136652,RMVar_hsa_circ_297077,RMVar_hsa_circ_324879,RMVar_hsa_circ_40466,RMVar_hsa_circ_136660,RMVar_hsa_circ_291675,RMVar_hsa_circ_136655,RMVar_hsa_circ_136656,RMVar_hsa_circ_136654,RMVar_hsa_circ_339529,RMVar_hsa_circ_340434,RMVar_hsa_circ_323095,RMVar_hsa_circ_273574,RMVar_hsa_circ_289095,RMVar_hsa_circ_136658,RMVar_hsa_circ_136659 52311 RMVar_ID_52311 Human_SNP_ID_801772289 A-to-I Human chr1 - 52772309 52772309 52772309 GAGGAACAGAAAGGATAAGGATGCTAAATTCCATCTGATTCTGATAGAGAGCCAGATTCACCGTT GAGGAACAGAAAGGATAAGGATGCTAAATTCCGTCTGATTCTGATAGAGAGCCAGATTCACCGTT T C RPS13P2 Ensembl:ENSG00000228929 Pseudogene exon GSE100210 HepG2 cell line chr1:52772308..52772309 29129909 RNA-Seq:(High) rs879110331 Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_1432683,Human_RBP_ID_1750474,Human_RBP_ID_5890045,Human_RBP_ID_8314412,Human_RBP_ID_17678190,Human_RBP_ID_18577655,Human_RBP_ID_26381340 Human_miRNA_ID_1840379,Human_miRNA_ID_1861689 52312 RMVar_ID_52312 Human_SNP_ID_801800686 A-to-I Human chr1 - 92468968 92468968 92468968 AGCCGGGCGTGGTGGCGGGCATCTGTGGTCCCAGCTACTTGGGAGGCTGAGGCGGGAGAATGGCA AGCCGGGCGTGGTGGCGGGCATCTGTGGTCCCGGCTACTTGGGAGGCTGAGGCGGGAGAATGGCA T C - - Other Unknown GSE100210 HepG2 cell line chr1:92468967..92468968 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 52313 RMVar_ID_52313 Human_SNP_ID_801829269 A-to-I Human chr1 - 23873668 23873668 23873668 TGCCCCCAATTCAGCTCCCTTGCCTCCTCCACACCCCTATTACATATAATAAGCAGAGCAAGTGG TGCCCCCAATTCAGCTCCCTTGCCTCCTCCACGCCCCTATTACATATAATAAGCAGAGCAAGTGG T C CNR2 Ensembl:ENSG00000188822 Protein coding 3'UTR GSE38233 cultured B-cells chr1:23873667..23873668 24183664 RNA-Seq:(High) rs6665733 Functional Loss SNV ICGC 33..33 33 SKCA 2 - 52314 RMVar_ID_52314 Human_SNP_ID_801830191 A-to-I Human chr1 + 32683885 32683885 32683885 GAACTCCTGACTCCAGGTGATCCACCCTCCTCAGCCTCCCAAAGTGCTAGGATTACAGGCGTGAG GAACTCCTGACTCCAGGTGATCCACCCTCCTCGGCCTCCCAAAGTGCTAGGATTACAGGCGTGAG A G RBBP4 Ensembl:ENSG00000162521 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line chr1:32683884..32683885 24183664,29129909,31158229 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue 52315 RMVar_ID_52315 Human_SNP_ID_801841683 A-to-I Human chr1 - 155899193 155899193 155899193 ATCTGAGCCTTGACCAAGTTTATCCTAAGGGAATACCACTTTGCTCCCTGTGCATAGTTTAGGAA ATCTGAGCCTTGACCAAGTTTATCCTAAGGGAGTACCACTTTGCTCCCTGTGCATAGTTTAGGAA T C RIT1 Ensembl:ENSG00000143622 Protein coding 3'UTR GSE38233 cultured B-cells chr1:155899192..155899193 24183664 RNA-Seq:(High) rs1055184 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_22373482,Human_RBP_ID_23335689,Human_RBP_ID_26388661 GWAS_ID_4065,GWAS_ID_4066,GWAS_ID_4067,GWAS_ID_4068 52316 RMVar_ID_52316 Human_SNP_ID_801858402 A-to-I Human chr1 - 208963441 208963441 208963441 GATTTTATGGCTAAGACTTTAAAAGCAAGGCAACAAAACCAAAAATAGACACATCGGACCATATT GATTTTATGGCTAAGACTTTAAAAGCAAGGCACCAAAACCAAAAATAGACACATCGGACCATATT T G - - Other Unknown GSE100210 HepG2 cell line chr1:208963440..208963441 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 52317 RMVar_ID_52317 Human_SNP_ID_801866265 A-to-I Human chr1 - 161116743 161116743 161116743 TTTCTGCCTTAGCCTCCCGAGTAGCTGGGATTACATGCCCGCACCACCACGCCCAGTTAATTTTT TTTCTGCCTTAGCCTCCCGAGTAGCTGGGATTGCATGCCCGCACCACCACGCCCAGTTAATTTTT T C PFDN2 Ensembl:ENSG00000143256 Protein coding intron GSE100210 HepG2 cell line chr1:161116742..161116743 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_124680,RMVar_hsa_circ_125716,RMVar_hsa_circ_137111,RMVar_hsa_circ_137116 52318 RMVar_ID_52318 Human_SNP_ID_801934233 A-to-I Human chr1 + 97546699 97546699 97546699 TTAATATCCATGCCATATCATGTGTGTACACTAAAAGATACAGAGGAAGTAGAGCTGAAGTTTCC TTAATATCCATGCCATATCATGTGTGTACACTGAAAGATACAGAGGAAGTAGAGCTGAAGTTTCC A G SEC63P1 Ensembl:ENSG00000228057 Pseudogene exon GSE100210 HepG2 cell line chr1:97546698..97546699 29129909 RNA-Seq:(High) rs1249756951 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue 52319 RMVar_ID_52319 Human_SNP_ID_801936779 A-to-I Human chr1 + 212615759 212615759 212615759 CCAGGAGGTTGAGGCTGCAATGAGCCGTGATCACCTCACTGCACTCCAGCCTGGGTGATGGAGCA CCAGGAGGTTGAGGCTGCAATGAGCCGTGATCGCCTCACTGCACTCCAGCCTGGGTGATGGAGCA A G ATF3 Ensembl:ENSG00000162772 Protein coding intron GSE47997 K562 cells&HepG2 cells chr1:212615758..212615759 23474544 RNA-Seq:(High) rs372572909 Functional Loss SNV ICGC 33..33 33 STAD 1 - RMVar_hsa_circ_49934,RMVar_hsa_circ_362277 52320 RMVar_ID_52320 Human_SNP_ID_801992665 A-to-I Human chr1 + 28335065 28335065 28335065 TTTTGGTTTTTGTTTTGTTTTGTTTTTGAGACAGAGTCTCGCTTTGTTTCCCAGGCTGGAGTGCA TTTTGGTTTTTGTTTTGTTTTGTTTTTGAGACGGAGTCTCGCTTTGTTTCCCAGGCTGGAGTGCA A G MED18 Ensembl:ENSG00000130772 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line chr1:28335064..28335065 24183664,29129909,31158229,31158229 RNA-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 52321 RMVar_ID_52321 Human_SNP_ID_801999445 A-to-I Human chr1 + 152399727 152399727 152399727 ACCCAAACCAAGAAAAACATCTGCTAAGAAAGAACCTGGAGCAAAGGTTAGCAGAGGTGCTAAAG ACCCAAACCAAGAAAAACATCTGCTAAGAAAGTACCTGGAGCAAAGGTTAGCAGAGGTGCTAAAG A T FLG-AS1,HMGN3P1 Ensembl:ENSG00000237975,Ensembl:ENSG00000183586 lincRNA,Pseudogene intron,exon GSE100210 HepG2 cell line chr1:152399727..152399728 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_5091316,Human_RBP_ID_5889701,Human_RBP_ID_8241092,Human_RBP_ID_10582989 52322 RMVar_ID_52322 Human_SNP_ID_801999497 A-to-I Human chr1 - 150223927 150223927 150223927 CAGCCTGACCAACATGGAGAAACCCTGTCTCTACTATAAATACAAAATTAGCTGGGCGTGGTGGC CAGCCTGACCAACATGGAGAAACCCTGTCTCTCCTATAAATACAAAATTAGCTGGGCGTGGTGGC T G ANP32E Ensembl:ENSG00000143401 Protein coding intron GSE38233 cultured B-cells chr1:150223926..150223927 24183664 RNA-Seq:(High) rs971911858 Functional Loss SNV ICGC 33..33 33 MALY 1 - RMVar_hsa_circ_368933 52323 RMVar_ID_52323 Human_SNP_ID_802012124 A-to-I Human chr1 + 245222258 245222257 245222258 CAGGAGTTCGAGACCAGCCTGGCCAACATGGTAAAACCCCGTCTCTACTAAAAATACAAAAATTA CAGGAGTTCGAGACCAGCCTGGCCAACATGGT_AAACCCCGTCTCTACTAAAAATACAAAAATTA TA T KIF26B Ensembl:ENSG00000162849 Protein coding intron GSE47997 K562 cells&HepG2 cells chr1:245222257..245222258;chr1:245222258..245222259 23474544 RNA-Seq:(High) - Functional Loss DEL ICGC 33..33 33 MALY 1 - 52324 RMVar_ID_52324 Human_SNP_ID_802066336 A-to-I Human chr1 - 65227635 65227635 65227635 AAGTTAGACAGGAGTCACTCCCAAGAATAGTAAAGGACACTCACTGGGGACAGTCATGATGGGTG AAGTTAGACAGGAGTCACTCCCAAGAATAGTAGAGGACACTCACTGGGGACAGTCATGATGGGTG T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr1:65227634..65227635 30559470 RNA-Seq:(High) rs866240256 Functional Loss SNV ICGC 33..33 33 PBCA 2 - 52325 RMVar_ID_52325 Human_SNP_ID_802097610 A-to-I Human chr1 + 52077047 52077047 52077047 AAAATTAGCCAGGCATGGTGGCACATGCCTGTAGTCCTACCAACCTAGGAGGCTGAGGCAGAAGG AAAATTAGCCAGGCATGGTGGCACATGCCTGTTGTCCTACCAACCTAGGAGGCTGAGGCAGAAGG A T BTF3L4 Ensembl:ENSG00000134717 Protein coding intron GSE38233 cultured B-cells chr1:52077046..52077047 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_122798,RMVar_hsa_circ_132924 52326 RMVar_ID_52326 Human_SNP_ID_802099416 A-to-I Human chr1 - 155924205 155924205 155924205 ATTCTGTCGCCTCCTGCCTCAGCGTCCCAAGTAGCTGGGACTATAGGCACCCGCCAACATGCCCG ATTCTGTCGCCTCCTGCCTCAGCGTCCCAAGTCGCTGGGACTATAGGCACCCGCCAACATGCCCG T G KHDC4 Ensembl:ENSG00000132680 Protein coding intron GSE100210 HepG2 cell line chr1:155924204..155924205 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 4 breast RMVar_hsa_circ_117053,RMVar_hsa_circ_55665,RMVar_hsa_circ_136725,RMVar_hsa_circ_66635,RMVar_hsa_circ_55113,RMVar_hsa_circ_74417,RMVar_hsa_circ_97864,RMVar_hsa_circ_136727,RMVar_hsa_circ_285323,RMVar_hsa_circ_298880,RMVar_hsa_circ_108867,RMVar_hsa_circ_125324,RMVar_hsa_circ_101961,RMVar_hsa_circ_136732,RMVar_hsa_circ_136734,RMVar_hsa_circ_136735,RMVar_hsa_circ_136733,RMVar_hsa_circ_334796,RMVar_hsa_circ_376919 52327 RMVar_ID_52327 Human_SNP_ID_802102616 A-to-I Human chr1 + 10356938 10356938 10356938 ATAAATAAATAAATAAATAAATAAAGTGCGGTAGCATGATCATAGCTCACTGCAACCTTGAATTC ATAAATAAATAAATAAATAAATAAAGTGCGGTGGCATGATCATAGCTCACTGCAACCTTGAATTC A G KIF1B Ensembl:ENSG00000054523 Protein coding intron GSE100210 HepG2 cell line chr1:10356937..10356938 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - RMVar_hsa_circ_1562,RMVar_hsa_circ_128954,RMVar_hsa_circ_6417,RMVar_hsa_circ_1629,RMVar_hsa_circ_357406,RMVar_hsa_circ_266934,RMVar_hsa_circ_312306,RMVar_hsa_circ_331163,RMVar_hsa_circ_54197,RMVar_hsa_circ_25153,RMVar_hsa_circ_11936,RMVar_hsa_circ_330528,RMVar_hsa_circ_6180,RMVar_hsa_circ_265623,RMVar_hsa_circ_59557,RMVar_hsa_circ_128965,RMVar_hsa_circ_128966,RMVar_hsa_circ_34774,RMVar_hsa_circ_370095,RMVar_hsa_circ_128969,RMVar_hsa_circ_21136,RMVar_hsa_circ_21757,RMVar_hsa_circ_11489 52328 RMVar_ID_52328 Human_SNP_ID_802109431 A-to-I Human chr1 - 151455942 151455942 151455942 GCCCAGGAGTTGGAGTTGAGCCTGGTCAGCATAGTGAGACCCTGTCTCTATTTATTAAAAAAAAA GCCCAGGAGTTGGAGTTGAGCCTGGTCAGCATGGTGAGACCCTGTCTCTATTTATTAAAAAAAAA T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,frontal_cortex chr1:151455941..151455942 29129909,30559470 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 UTCA,endometrium carcinosarcoma-malignant_mesodermal_mixed_tumour 11 uterus Human_RBP_ID_5690057 52329 RMVar_ID_52329 Human_SNP_ID_802115956 A-to-I Human chr1 - 219980779 219980779 219980779 TTCTTTGGCAGGAAGGGCACAGTGCTTTTGCTACCATGGAAGAGGCAGCGGAAGAGGTATAAAAA TTCTTTGGCAGGAAGGGCACAGTGCTTTTGCTCCCATGGAAGAGGCAGCGGAAGAGGTATAAAAA T G EPRS1 Ensembl:ENSG00000136628 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector chr1:219980778..219980779 29967493 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUSC 2 lung Human_RBP_ID_803241,Human_RBP_ID_8755332,Human_RBP_ID_9253133,Human_RBP_ID_9270605,Human_RBP_ID_17338656,Human_RBP_ID_22429972,Human_RBP_ID_22749757,Human_RBP_ID_22782157 Human_Splice_Rec_188738,Human_Splice_Rec_188739 RMVar_hsa_circ_72176,RMVar_hsa_circ_139641,RMVar_hsa_circ_78102,RMVar_hsa_circ_83605,RMVar_hsa_circ_126425,RMVar_hsa_circ_139642,RMVar_hsa_circ_139643,RMVar_hsa_circ_72680,RMVar_hsa_circ_139644,RMVar_hsa_circ_105348,RMVar_hsa_circ_115619,RMVar_hsa_circ_20395,RMVar_hsa_circ_57254,RMVar_hsa_circ_61526,RMVar_hsa_circ_52389,RMVar_hsa_circ_139648,RMVar_hsa_circ_362524,RMVar_hsa_circ_139646,RMVar_hsa_circ_345463,RMVar_hsa_circ_139647 52330 RMVar_ID_52330 Human_SNP_ID_802115960 A-to-I Human chr1 - 219980779 219980779 219980779 TTCTTTGGCAGGAAGGGCACAGTGCTTTTGCTACCATGGAAGAGGCAGCGGAAGAGGTATAAAAA TTCTTTGGCAGGAAGGGCACAGTGCTTTTGCTGCCATGGAAGAGGCAGCGGAAGAGGTATAAAAA T C EPRS1 Ensembl:ENSG00000136628 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector chr1:219980778..219980779 29967493 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus Human_RBP_ID_803241,Human_RBP_ID_8755332,Human_RBP_ID_9253133,Human_RBP_ID_9270605,Human_RBP_ID_17338656,Human_RBP_ID_22429972,Human_RBP_ID_22749757,Human_RBP_ID_22782157 Human_Splice_Rec_188738,Human_Splice_Rec_188739 RMVar_hsa_circ_72176,RMVar_hsa_circ_139641,RMVar_hsa_circ_78102,RMVar_hsa_circ_83605,RMVar_hsa_circ_126425,RMVar_hsa_circ_139642,RMVar_hsa_circ_139643,RMVar_hsa_circ_72680,RMVar_hsa_circ_139644,RMVar_hsa_circ_105348,RMVar_hsa_circ_115619,RMVar_hsa_circ_20395,RMVar_hsa_circ_57254,RMVar_hsa_circ_61526,RMVar_hsa_circ_52389,RMVar_hsa_circ_139648,RMVar_hsa_circ_362524,RMVar_hsa_circ_139646,RMVar_hsa_circ_345463,RMVar_hsa_circ_139647 52331 RMVar_ID_52331 Human_SNP_ID_802124317 A-to-I Human chr1 - 154209751 154209751 154209751 GTCTCTACTAAAAATACAAAAAAAAAAAAATTAGCCGGGCGTGGTGGCGGGTGCCTGTAGTCCCA GTCTCTACTAAAAATACAAAAAAAAAAAAATTTGCCGGGCGTGGTGGCGGGTGCCTGTAGTCCCA T A C1orf43 Ensembl:ENSG00000143612 Protein coding intron GSE38233 cultured B-cells chr1:154209750..154209751 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 STAD 1 - RMVar_hsa_circ_136359,RMVar_hsa_circ_121933 52332 RMVar_ID_52332 Human_SNP_ID_802132190 A-to-I Human chr1 - 32649132 32649132 32649132 GAAACCCCGTCTCTACTAAAAATACAAAAATTAGCTGCGCATGATGGTGGGCGCCTGTAATCCCA GAAACCCCGTCTCTACTAAAAATACAAAAATTTGCTGCGCATGATGGTGGGCGCCTGTAATCCCA T A ZBTB8OS Ensembl:ENSG00000176261 Protein coding intron GSE100210 HepG2 cell line chr1:32649131..32649132 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_99545,RMVar_hsa_circ_131266 52333 RMVar_ID_52333 Human_SNP_ID_802162417 A-to-I Human chr1 - 109418423 109418423 109418423 TAGTCTTAGCTATTTTGCAGGCTTAGGTGGGAAGATCTCGTGAGCCTGGGAGGTTGGGGCTCCAT TAGTCTTAGCTATTTTGCAGGCTTAGGTGGGACGATCTCGTGAGCCTGGGAGGTTGGGGCTCCAT T G PSMA5 Ensembl:ENSG00000143106 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr1:109418422..109418423 24183664,29129909 RNA-Seq:(High) rs1039778391 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_22563844 RMVar_hsa_circ_135214,RMVar_hsa_circ_348759,RMVar_hsa_circ_121549,RMVar_hsa_circ_299088 52334 RMVar_ID_52334 Human_SNP_ID_802176325 A-to-I Human chr1 - 153875019 153875019 153875019 AAAAAATGCTGGGCATGGTGGCATGTCCCTGTAGTCCCAGTTAGTTGGGAGGCTGAGGTGGGAAG AAAAAATGCTGGGCATGGTGGCATGTCCCTGTTGTCCCAGTTAGTTGGGAGGCTGAGGTGGGAAG T A GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE100210 HepG2 cell line chr1:153875018..153875019 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_17558000,Human_RBP_ID_24589767 52335 RMVar_ID_52335 Human_SNP_ID_802201864 A-to-I Human chr1 - 31469399 31469399 31469399 TAATTGAAGGTCGTCTTGGTGTTGGGCTTCTTAAACCCTGTGTGTCTCCCTATAACACTCCAATA TAATTGAAGGTCGTCTTGGTGTTGGGCTTCTTTAACCCTGTGTGTCTCCCTATAACACTCCAATA T A lnc-FABP3-2,lnc-FABP3-2:2,lnc-FABP3-2:3 RNACentral:URS00008B36C2,RNACentral:URS00009C356E,RNACentral:URS0000E92232 lincRNA,lincRNA,lincRNA intron,intron,intron GSE100210 HepG2 cell line chr1:31469398..31469399 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 52336 RMVar_ID_52336 Human_SNP_ID_802230723 A-to-I Human chr1 - 72274753 72274753 72274753 ACAGCTGGGGTCACAGATGAACTGCTTACAGCAAGCAATTTCTCCTTCCGATTTTACTCCAATTA ACAGCTGGGGTCACAGATGAACTGCTTACAGCGAGCAATTTCTCCTTCCGATTTTACTCCAATTA T C NEGR1 Ensembl:ENSG00000172260 Protein coding intron GSE100210 HepG2 cell line chr1:72274752..72274753 29129909 RNA-Seq:(High) rs879069725 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue 52337 RMVar_ID_52337 Human_SNP_ID_802276602 A-to-I Human chr1 - 179112705 179112705 179112705 CACACCCATAGTCCCAGCTACTTGGGGAGCTGAGGCAGGAGGATTGTTTGAACCCAGGAGGTCAA CACACCCATAGTCCCAGCTACTTGGGGAGCTGCGGCAGGAGGATTGTTTGAACCCAGGAGGTCAA T G ABL2 Ensembl:ENSG00000143322 Protein coding intron GSE100210 HepG2 cell line chr1:179112704..179112705 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - RMVar_hsa_circ_7271,RMVar_hsa_circ_43641,RMVar_hsa_circ_308320,RMVar_hsa_circ_364889,RMVar_hsa_circ_50699,RMVar_hsa_circ_273320,RMVar_hsa_circ_315087,RMVar_hsa_circ_337138,RMVar_hsa_circ_84467,RMVar_hsa_circ_44890,RMVar_hsa_circ_137954,RMVar_hsa_circ_137951,RMVar_hsa_circ_137950,RMVar_hsa_circ_89129,RMVar_hsa_circ_297448,RMVar_hsa_circ_373438,RMVar_hsa_circ_367757,RMVar_hsa_circ_320300,RMVar_hsa_circ_284843,RMVar_hsa_circ_137957,RMVar_hsa_circ_137959,RMVar_hsa_circ_137960,RMVar_hsa_circ_137961,RMVar_hsa_circ_137958,RMVar_hsa_circ_137956 52338 RMVar_ID_52338 Human_SNP_ID_802327740 A-to-I Human chr1 + 51752485 51752485 51752485 TTTACACGATATATTTGTTTGTTTATCTCTTTATTGACTGTCTACCCTAGAGTACAATCTTGGTG TTTACACGATATATTTGTTTGTTTATCTCTTTGTTGACTGTCTACCCTAGAGTACAATCTTGGTG A G OSBPL9 Ensembl:ENSG00000117859 Protein coding intron GSE100210 HepG2 cell line chr1:51752484..51752485 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 9 haematopoietic and lymphoid tissue Human_RBP_ID_3316344,Human_RBP_ID_19379593,Human_RBP_ID_22707990 RMVar_hsa_circ_132853,RMVar_hsa_circ_86879,RMVar_hsa_circ_356575,RMVar_hsa_circ_364066,RMVar_hsa_circ_102747,RMVar_hsa_circ_67836,RMVar_hsa_circ_15550,RMVar_hsa_circ_65077,RMVar_hsa_circ_132855,RMVar_hsa_circ_34789,RMVar_hsa_circ_280792,RMVar_hsa_circ_301273,RMVar_hsa_circ_273705,RMVar_hsa_circ_39352,RMVar_hsa_circ_62476,RMVar_hsa_circ_32843,RMVar_hsa_circ_132856,RMVar_hsa_circ_132857,RMVar_hsa_circ_132858,RMVar_hsa_circ_313159,RMVar_hsa_circ_317627,RMVar_hsa_circ_127458,RMVar_hsa_circ_22885,RMVar_hsa_circ_72256,RMVar_hsa_circ_301237,RMVar_hsa_circ_132859,RMVar_hsa_circ_277874,RMVar_hsa_circ_278918,RMVar_hsa_circ_132860,RMVar_hsa_circ_291943,RMVar_hsa_circ_272051,RMVar_hsa_circ_132862,RMVar_hsa_circ_132863,RMVar_hsa_circ_132861 52339 RMVar_ID_52339 Human_SNP_ID_802332580 A-to-I Human chr1 + 38709518 38709518 38709518 TTGCTGACCTAAATGTTATGAGGATCATCAATAAGCCTACAGCAGCTGCTATTGCTTATGGCCTG TTGCTGACCTAAATGTTATGAGGATCATCAATGAGCCTACAGCAGCTGCTATTGCTTATGGCCTG A G HSPA5P1 Ensembl:ENSG00000215895 Pseudogene exon GSE100210 HepG2 cell line chr1:38709517..38709518 29129909 RNA-Seq:(High) rs878915998 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_miRNA_ID_1876494 52340 RMVar_ID_52340 Human_SNP_ID_802401188 A-to-I Human chr1 - 23874479 23874479 23874479 AACTCAAGTCAGAAATCAGTTCACTCCCTGGAAGAGAGAGAGGGGTCTTGGCACTCTCTTCTTAC AACTCAAGTCAGAAATCAGTTCACTCCCTGGAGGAGAGAGAGGGGTCTTGGCACTCTCTTCTTAC T C CNR2 Ensembl:ENSG00000188822 Protein coding 3'UTR GSE38233 cultured B-cells chr1:23874478..23874479 24183664 RNA-Seq:(High) rs2229584 Functional Loss SNV ICGC 33..33 33 COCA 2 - 52341 RMVar_ID_52341 Human_SNP_ID_802420738 A-to-I Human chr1 + 166276796 166276796 166276796 ATAAACACCCATGCTACTGGGGTGGTCCTGTCAGAATGAACTCTGCTGCCCGTAGCTGCTGCTCT ATAAACACCCATGCTACTGGGGTGGTCCTGTCGGAATGAACTCTGCTGCCCGTAGCTGCTGCTCT A G AL596087.2 Ensembl:ENSG00000229588 lincRNA intron GSE100210 HepG2 cell line chr1:166276795..166276796 29129909 RNA-Seq:(High) rs879048038 Functional Loss SNV ICGC 33..33 33 LAML 2 - 52342 RMVar_ID_52342 Human_SNP_ID_802438257 A-to-I Human chr1 - 161065113 161065113 161065113 AAAATTAGCAGGGCATGGTGGCGTGCACCTGTAGTCCTGGCTACTCAGGAGGCTGAGGCACCAGA AAAATTAGCAGGGCATGGTGGCGTGCACCTGTGGTCCTGGCTACTCAGGAGGCTGAGGCACCAGA T C ARHGAP30 Ensembl:ENSG00000186517 Protein coding intron GSE38233 cultured B-cells chr1:161065112..161065113 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 52343 RMVar_ID_52343 Human_SNP_ID_802460310 A-to-I Human chr1 + 225787046 225787046 225787046 TAAATTTTTTTGTCAAGACAGGGTCTCATTATATTGCCCAGGTTGATCTGGAACTCCTGGACTCA TAAATTTTTTTGTCAAGACAGGGTCTCATTATGTTGCCCAGGTTGATCTGGAACTCCTGGACTCA A G SRP9 Ensembl:ENSG00000143742 Protein coding intron GSE47997;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line chr1:225787045..225787046 23474544,29129909,31158229,31158229,31158229,32596459 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_10807872,Human_RBP_ID_17557434 RMVar_hsa_circ_140054,RMVar_hsa_circ_84583 52344 RMVar_ID_52344 Human_SNP_ID_802473252 A-to-I Human chr1 + 119158210 119158210 119158210 TCACCCAGGCTAGAGTGCACAGGTAAAATCATAGCTCACTGTAGCCTCAATCTCCTGGCCTCAAG TCACCCAGGCTAGAGTGCACAGGTAAAATCATGGCTCACTGTAGCCTCAATCTCCTGGCCTCAAG A G WARS2-AS1 Ensembl:ENSG00000231365 lincRNA intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line chr1:119158209..119158210 29129909,31158229 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - RMVar_hsa_circ_86930,RMVar_hsa_circ_135731 52345 RMVar_ID_52345 Human_SNP_ID_802498673 A-to-I Human chr1 - 97546345 97546345 97546345 TCATCTTCCTTTACTGCAGCTTCATTCCCAACAACTCCATTTGCCAGCTTTTGTTTCTGTTGCTT TCATCTTCCTTTACTGCAGCTTCATTCCCAACGACTCCATTTGCCAGCTTTTGTTTCTGTTGCTT T C DPYD Ensembl:ENSG00000188641 Protein coding intron GSE107867 ASD brains,frontal_cortex chr1:97546344..97546345 30559470 RNA-Seq:(High) rs959420245 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue 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 52346 RMVar_ID_52346 Human_SNP_ID_802503439 A-to-I Human chr1 - 1396541 1396541 1396541 AACAGCCTTGCCGAGCGCAGTGGCTCACGCCTATAGTCCCAGCACTTTGGGAGGCCAAGGCGGGT AACAGCCTTGCCGAGCGCAGTGGCTCACGCCTGTAGTCCCAGCACTTTGGGAGGCCAAGGCGGGT T C CCNL2 Ensembl:ENSG00000221978 Protein coding intron GSE38233 cultured B-cells chr1:1396540..1396541 24183664 RNA-Seq:(High) rs1213929473 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue RMVar_hsa_circ_54913,RMVar_hsa_circ_299083,RMVar_hsa_circ_128326 52347 RMVar_ID_52347 Human_SNP_ID_802523076 A-to-I Human chr1 + 26764001 26763997 26764001 TTATATTTATTTATTTATTTAGAGACTGTCTCACTCTGTTGCCCAAGCTGGAGTGTAATGGCACA TTATATTTATTTATTTATTTAGAGACTGT____CTCTGTTGCCCAAGCTGGAGTGTAATGGCACA TCTCA T ARID1A Ensembl:ENSG00000117713 Protein coding intron GSE100210 HepG2 cell line chr1:26764000..26764001 29129909 RNA-Seq:(High) rs1376995215 Functional Loss DEL ICGC 30..33 33 LICA 1 - RMVar_hsa_circ_49434,RMVar_hsa_circ_130679,RMVar_hsa_circ_109031,RMVar_hsa_circ_266788,RMVar_hsa_circ_95019,RMVar_hsa_circ_130680,RMVar_hsa_circ_61331,RMVar_hsa_circ_25221,RMVar_hsa_circ_50375 52348 RMVar_ID_52348 Human_SNP_ID_802527609 A-to-I Human chr1 - 16130768 16130768 16130768 AAAATTAGCCAAGTGTGTTGGCACGTGCCTGTAGTCTCAGCTACTCAGGAGGCGGAGGTGGGAGG AAAATTAGCCAAGTGTGTTGGCACGTGCCTGTGGTCTCAGCTACTCAGGAGGCGGAGGTGGGAGG T C EPHA2 Ensembl:ENSG00000142627 Protein coding intron GSE100210 HepG2 cell line chr1:16130767..16130768 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 RECA 1 - 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 52349 RMVar_ID_52349 Human_SNP_ID_802537112 A-to-I Human chr1 + 75731783 75731783 75731783 ATGGTGTCTCATGCTTGTAATCCCAGCACTTTAGGAGACCACGGCAGGAGGATTGCTTGAGGCCA ATGGTGTCTCATGCTTGTAATCCCAGCACTTTGGGAGACCACGGCAGGAGGATTGCTTGAGGCCA A G ACADM Ensembl:ENSG00000117054 Protein coding intron GSE38233 cultured B-cells chr1:75731782..75731783 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 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 52350 RMVar_ID_52350 Human_SNP_ID_802538708 A-to-I Human chr1 + 93227831 93227831 93227831 ATTAAAAACATTAGCCAGGTATGGTGGTGCATACCCGTGGTCCCAGCTACTCAGGAAGCTGAGAT ATTAAAAACATTAGCCAGGTATGGTGGTGCATGCCCGTGGTCCCAGCTACTCAGGAAGCTGAGAT A G CCDC18 Ensembl:ENSG00000122483 Protein coding intron GSE100210 HepG2 cell line chr1:93227830..93227831 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_50772,RMVar_hsa_circ_60118,RMVar_hsa_circ_92842,RMVar_hsa_circ_353083,RMVar_hsa_circ_134609,RMVar_hsa_circ_355809,RMVar_hsa_circ_367955,RMVar_hsa_circ_339136,RMVar_hsa_circ_322437,RMVar_hsa_circ_61081,RMVar_hsa_circ_71024,RMVar_hsa_circ_61338,RMVar_hsa_circ_352103,RMVar_hsa_circ_347359,RMVar_hsa_circ_266059,RMVar_hsa_circ_60417,RMVar_hsa_circ_329335,RMVar_hsa_circ_134614,RMVar_hsa_circ_372568,RMVar_hsa_circ_362352,RMVar_hsa_circ_377863,RMVar_hsa_circ_333149,RMVar_hsa_circ_35777,RMVar_hsa_circ_298656,RMVar_hsa_circ_134616,RMVar_hsa_circ_324930,RMVar_hsa_circ_134621,RMVar_hsa_circ_73399,RMVar_hsa_circ_368503,RMVar_hsa_circ_355904,RMVar_hsa_circ_67100,RMVar_hsa_circ_280678,RMVar_hsa_circ_59405,RMVar_hsa_circ_329456,RMVar_hsa_circ_364796,RMVar_hsa_circ_350075,RMVar_hsa_circ_358641,RMVar_hsa_circ_365638,RMVar_hsa_circ_320875,RMVar_hsa_circ_7930,RMVar_hsa_circ_73793,RMVar_hsa_circ_58012,RMVar_hsa_circ_134622,RMVar_hsa_circ_336430,RMVar_hsa_circ_134623 52351 RMVar_ID_52351 Human_SNP_ID_802542756 A-to-I Human chr1 - 70351078 70351078 70351078 GCTCTTGCTGTAGTCTCTGCCTCCCGGGTTCAAGTGATGCTTCTGCCTCAGCCTCCTGAGTAGCT GCTCTTGCTGTAGTCTCTGCCTCCCGGGTTCATGTGATGCTTCTGCCTCAGCCTCCTGAGTAGCT T A ANKRD13C Ensembl:ENSG00000118454 Protein coding intron GSE100210 HepG2 cell line chr1:70351077..70351078 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 3 pancreas Human_RBP_ID_11098084 52352 RMVar_ID_52352 Human_SNP_ID_802546149 A-to-I Human chr1 + 150308756 150308756 150308756 TACTTGGGTGGCTGAGGCAGGAGAATTGCTTGAACTGGGGAGGAAGAGGTTGCAGTGAGCCAAGA TACTTGGGTGGCTGAGGCAGGAGAATTGCTTGGACTGGGGAGGAAGAGGTTGCAGTGAGCCAAGA A G MRPS21 Ensembl:ENSG00000266472 Protein coding 3'UTR GSE38233;GSE100210;GSE100210;GSE99789;GSE99789;GSE107867;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;HepG2 cell line;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;Bronchiolar epithelium,BERP35T4 cell line chr1:150308755..150308756;chr1:150308756..150308757 24183664,29129909,29129909,29796672,29796672,30559470,31158229 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 haematopoietic and lymphoid tissue 52353 RMVar_ID_52353 Human_SNP_ID_802547262 A-to-I Human chr1 - 31290061 31290057 31290061 TGAGCCCAGTTCAAGACCAGCCTGGGCAACATAGTGAGACCTTGCCTCTACAAATGATTTTTAAA TGAGCCCAGTTCAAGACCAGCCTGGGCAACAT____AGACCTTGCCTCTACAAATGATTTTTAAA TCACT T SNRNP40 Ensembl:ENSG00000060688 Protein coding intron GSE100210 HepG2 cell line chr1:31290060..31290061 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 33..36 33 LMS 1 - RMVar_hsa_circ_79760,RMVar_hsa_circ_50169,RMVar_hsa_circ_131049,RMVar_hsa_circ_310173,RMVar_hsa_circ_131051,RMVar_hsa_circ_131052,RMVar_hsa_circ_313377,RMVar_hsa_circ_287591,RMVar_hsa_circ_131053,RMVar_hsa_circ_28023,RMVar_hsa_circ_334221,RMVar_hsa_circ_338815 52354 RMVar_ID_52354 Human_SNP_ID_802552277 A-to-I Human chr1 - 229451244 229451244 229451244 CAGGTGTGCACCACTGTACCCAGCTAATTTTTATACTTTTTGTAGAGACGAGGTTTCTCCATGTT CAGGTGTGCACCACTGTACCCAGCTAATTTTTGTACTTTTTGTAGAGACGAGGTTTCTCCATGTT T C NUP133 Ensembl:ENSG00000069248 Protein coding intron GSE100210 HepG2 cell line chr1:229451243..229451244 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_10828222,Human_RBP_ID_24651184 RMVar_hsa_circ_21411,RMVar_hsa_circ_81578,RMVar_hsa_circ_91523,RMVar_hsa_circ_95693,RMVar_hsa_circ_24928,RMVar_hsa_circ_323393,RMVar_hsa_circ_140259,RMVar_hsa_circ_140260,RMVar_hsa_circ_140261,RMVar_hsa_circ_345106,RMVar_hsa_circ_328469,RMVar_hsa_circ_306068,RMVar_hsa_circ_48105,RMVar_hsa_circ_140268,RMVar_hsa_circ_140265,RMVar_hsa_circ_140266,RMVar_hsa_circ_363633,RMVar_hsa_circ_291230,RMVar_hsa_circ_118325,RMVar_hsa_circ_140267,RMVar_hsa_circ_306351,RMVar_hsa_circ_73674,RMVar_hsa_circ_140269,RMVar_hsa_circ_140270 52355 RMVar_ID_52355 Human_SNP_ID_802578259 A-to-I Human chr1 + 201995526 201995525 201995526 GCAACATAGCGAAACCCTACCTCTACAAAAATAAAAAAATTAGCCAGGCATGATGATGTGCAACT GCAACATAGCGAAACCCTACCTCTACAAAAAT_AAAAAATTAGCCAGGCATGATGATGTGCAACT TA T RNPEP Ensembl:ENSG00000176393 Protein coding intron GSE47997 K562 cells&HepG2 cells chr1:201995526..201995527 23474544 RNA-Seq:(High) - Functional Loss DEL ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_138892,RMVar_hsa_circ_17858,RMVar_hsa_circ_86896,RMVar_hsa_circ_294835,RMVar_hsa_circ_329060,RMVar_hsa_circ_302797,RMVar_hsa_circ_29513,RMVar_hsa_circ_138894,RMVar_hsa_circ_138895,RMVar_hsa_circ_138896,RMVar_hsa_circ_138893 52356 RMVar_ID_52356 Human_SNP_ID_802595145 A-to-I Human chr1 - 44661406 44661406 44661406 CAAACCCCCTTTTTTACTCTTAAAAAAAAAAAAAGAAAAAGAAAGCTGCACATGGTGGTGGGTGC CAAACCCCCTTTTTTACTCTTAAAAAAAAAAAGAGAAAAAGAAAGCTGCACATGGTGGTGGGTGC T C TMEM53 Ensembl:ENSG00000126106 Protein coding intron GSE100210 HepG2 cell line chr1:44661405..44661406 29129909 RNA-Seq:(High) rs1010531434 Functional Loss SNV ICGC,COSMIC 33..33 33 UTCA,endometrium carcinosarcoma-malignant_mesodermal_mixed_tumour 6 uterus 52357 RMVar_ID_52357 Human_SNP_ID_802605786 A-to-I Human chr1 - 160222763 160222763 160222763 ATTTATCATTTCAGTAAAAGGCGTCAATTTCTATGGCCCCAAGAGTGAGTTTGTGGTGAGCGGTA ATTTATCATTTCAGTAAAAGGCGTCAATTTCTGTGGCCCCAAGAGTGAGTTTGTGGTGAGCGGTA T C DCAF8,AL139011.2 Ensembl:ENSG00000132716,Ensembl:ENSG00000258465 Protein coding,Protein coding CDS,3'UTR GSE112787 293 Flip-In T-REx cells,empty vector chr1:160222762..160222763 29967493 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 brain oligodendroglioma,central_nervous_system oligodendroglioma 4 brain Human_RBP_ID_3283573 Human_Splice_Rec_147190,Human_Splice_Rec_147216,Human_Splice_Rec_147242,Human_Splice_Rec_147250,Human_Splice_Rec_147278,Human_Splice_Rec_147288,Human_Splice_Rec_147318,Human_Splice_Rec_147374,Human_Splice_Rec_147408 Human_miRNA_ID_496616,Human_miRNA_ID_496617 RMVar_hsa_circ_93317,RMVar_hsa_circ_123319,RMVar_hsa_circ_103147,RMVar_hsa_circ_74628,RMVar_hsa_circ_137002,RMVar_hsa_circ_137003,RMVar_hsa_circ_137004,RMVar_hsa_circ_137006,RMVar_hsa_circ_346799,RMVar_hsa_circ_376103,RMVar_hsa_circ_109951,RMVar_hsa_circ_137005,RMVar_hsa_circ_342606 52358 RMVar_ID_52358 Human_SNP_ID_802646992 A-to-I Human chr1 - 19158979 19158979 19158979 CACCATCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGATAGGATTTCACCATGTTGCCCAGAA CACCATCATGCCTGGCTAATTTTTGTATTTTTGGTAGAGATAGGATTTCACCATGTTGCCCAGAA T C UBR4 Ensembl:ENSG00000127481 Protein coding intron GSE38233 cultured B-cells chr1:19158978..19158979 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 UTCA,endometrium carcinosarcoma-malignant_mesodermal_mixed_tumour 3 uterus 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_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 52359 RMVar_ID_52359 Human_SNP_ID_802664756 A-to-I Human chr1 + 150468051 150468051 150468051 GGGCGTGGTGGCTCACAGCTGTAACCCCAACTACTTGGGAGGCTGAGGTAGGAGAATCGCTTGAA GGGCGTGGTGGCTCACAGCTGTAACCCCAACTGCTTGGGAGGCTGAGGTAGGAGAATCGCTTGAA A G RPRD2 Ensembl:ENSG00000163125 Protein coding intron GSE38233 cultured B-cells chr1:150468050..150468051 24183664 RNA-Seq:(High) rs994171904 Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 3 breast RMVar_hsa_circ_135899,RMVar_hsa_circ_109119 52360 RMVar_ID_52360 Human_SNP_ID_802693413 A-to-I Human chr1 - 155907978 155907978 155907978 TCATGCCATTCTCCTGCCTCAGGCTCCAGCGTAGCTGGGACTACAGGCACCCGCCACCTCGCCTG TCATGCCATTCTCCTGCCTCAGGCTCCAGCGTGGCTGGGACTACAGGCACCCGCCACCTCGCCTG T C RIT1 Ensembl:ENSG00000143622 Protein coding intron GSE38233 cultured B-cells chr1:155907977..155907978 24183664 RNA-Seq:(High) rs656247 Functional Loss SNV ICGC 33..33 33 LAML 1 - RMVar_hsa_circ_81183,RMVar_hsa_circ_136724 52361 RMVar_ID_52361 Human_SNP_ID_802694623 A-to-I Human chr1 + 51752547 51752547 51752547 GTGAGGAATTTGCTCGTCTTACCACTTGTATTAGTCTGCATGGGCTGCCATAACAAAATACCATA GTGAGGAATTTGCTCGTCTTACCACTTGTATTGGTCTGCATGGGCTGCCATAACAAAATACCATA A G OSBPL9 Ensembl:ENSG00000117859 Protein coding intron GSE100210 HepG2 cell line chr1:51752546..51752547 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 9 haematopoietic and lymphoid tissue Human_RBP_ID_22707990 Human_Splice_Rec_69460 RMVar_hsa_circ_132853,RMVar_hsa_circ_86879,RMVar_hsa_circ_356575,RMVar_hsa_circ_364066,RMVar_hsa_circ_102747,RMVar_hsa_circ_67836,RMVar_hsa_circ_15550,RMVar_hsa_circ_65077,RMVar_hsa_circ_132855,RMVar_hsa_circ_34789,RMVar_hsa_circ_280792,RMVar_hsa_circ_301273,RMVar_hsa_circ_273705,RMVar_hsa_circ_39352,RMVar_hsa_circ_62476,RMVar_hsa_circ_32843,RMVar_hsa_circ_132856,RMVar_hsa_circ_132857,RMVar_hsa_circ_132858,RMVar_hsa_circ_313159,RMVar_hsa_circ_317627,RMVar_hsa_circ_127458,RMVar_hsa_circ_22885,RMVar_hsa_circ_72256,RMVar_hsa_circ_301237,RMVar_hsa_circ_132859,RMVar_hsa_circ_277874,RMVar_hsa_circ_278918,RMVar_hsa_circ_132860,RMVar_hsa_circ_291943,RMVar_hsa_circ_272051,RMVar_hsa_circ_132862,RMVar_hsa_circ_132863,RMVar_hsa_circ_132861 52362 RMVar_ID_52362 Human_SNP_ID_802759692 A-to-I Human chr1 - 154208232 154208232 154208232 GCCACCATACCTGGCTAATTTTTTGCAGAGATAGGGTCTCACTTTGTTTCCCAGACTGGTCTCAA GCCACCATACCTGGCTAATTTTTTGCAGAGATTGGGTCTCACTTTGTTTCCCAGACTGGTCTCAA T A C1orf43 Ensembl:ENSG00000143612 Protein coding intron GSE38233 cultured B-cells chr1:154208231..154208232 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 6 oesophagus RMVar_hsa_circ_136359,RMVar_hsa_circ_121933 52363 RMVar_ID_52363 Human_SNP_ID_802761470 A-to-I Human chr1 - 100210090 100210090 100210090 CCCAGGCTGGTCTTGAACTTCTGGTCTAAGCAATCCTCCTGCCTCAGCCTCCCAAAGTGCTGGGA CCCAGGCTGGTCTTGAACTTCTGGTCTAAGCAGTCCTCCTGCCTCAGCCTCCCAAAGTGCTGGGA T C DBT Ensembl:ENSG00000137992 Protein coding intron GSE100210 HepG2 cell line chr1:100210089..100210090 29129909 RNA-Seq:(High) rs1176599207 Functional Loss SNV ICGC,COSMIC 33..33 33 NKTL,haematopoietic_and_lymphoid_tissue NK-T_cell_lymphoma 2 haematopoietic and lymphoid tissue RMVar_hsa_circ_12161,RMVar_hsa_circ_32764,RMVar_hsa_circ_134929,RMVar_hsa_circ_295112,RMVar_hsa_circ_378510,RMVar_hsa_circ_134930,RMVar_hsa_circ_134931 52364 RMVar_ID_52364 Human_SNP_ID_802763975 A-to-I Human chr1 + 113131048 113131048 113131048 CGCCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGAATTAATTACAGACG CGCCTCCCAGGTTCAAGCGATTCTCCTGCCTCGGCCTCCCAAGTAGCTGGAATTAATTACAGACG A G LRIG2 Ensembl:ENSG00000198799 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line chr1:113131047..113131048 31158229 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 2 oesophagus 52365 RMVar_ID_52365 Human_SNP_ID_802781852 A-to-I Human chr1 + 155314225 155314225 155314225 TTTTTTTTTTTGATACAGGGTCTTACTCTGTTACCCAGGCTGGAGTGCAGTGGCATGATCTTGGC TTTTTTTTTTTGATACAGGGTCTTACTCTGTTGCCCAGGCTGGAGTGCAGTGGCATGATCTTGGC A G FDPS Ensembl:ENSG00000160752 Protein coding intron GSE38233 cultured B-cells chr1:155314224..155314225 24183664 RNA-Seq:(High) rs190453202 Functional Loss SNV ICGC 33..33 33 PRAD 1 - Human_RBP_ID_11175411 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 52366 RMVar_ID_52366 Human_SNP_ID_802858263 A-to-I Human chr1 - 54524890 54524890 54524890 CTCTGCATTGAACATTCATTCTGTCAGCATCCACTCCAGCTTCACTGCGTCAGCAGCAGACTTGC CTCTGCATTGAACATTCATTCTGTCAGCATCCCCTCCAGCTTCACTGCGTCAGCAGCAGACTTGC T G - - Other Unknown GSE100210 HepG2 cell line chr1:54524889..54524890 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 52367 RMVar_ID_52367 Human_SNP_ID_802872475 A-to-I Human chr1 - 114566496 114566496 114566496 CTCCTGCCTCAGCCTCCTAAGTAGCTGGGATTACAGGCATGTGCCACTTCGCCCGGCTGATTTTG CTCCTGCCTCAGCCTCCTAAGTAGCTGGGATTGCAGGCATGTGCCACTTCGCCCGGCTGATTTTG T C - - Other Unknown GSE100210 HepG2 cell line chr1:114566495..114566496 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_111957,RMVar_hsa_circ_135549 52368 RMVar_ID_52368 Human_SNP_ID_802904114 A-to-I Human chr1 + 171496980 171496970 171496980 CCACCACACCTGGCTATTTTTTTGGTAGAGACAAGGTCTCTCCATGTTGCTCAGGCTGGTCTCAA CCACCACACCTGGCTATTTTTTT__________AGGTCTCTCCATGTTGCTCAGGCTGGTCTCAA TGGTAGAGACA T PRRC2C Ensembl:ENSG00000117523 Protein coding intron GSE100210 HepG2 cell line chr1:171496980..171496981 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 24..33 33 NKTL 1 - Human_RBP_ID_9556237,Human_RBP_ID_11188512,Human_RBP_ID_23344344 RMVar_hsa_circ_137515,RMVar_hsa_circ_107472,RMVar_hsa_circ_116819,RMVar_hsa_circ_137516 52369 RMVar_ID_52369 Human_SNP_ID_802917436 A-to-I Human chr1 - 29174179 29174179 29174179 TTTTTTCTTTTTTTTTTTGAGATGGGGTCTCAATCTGTCTCCCAGGCTGCAGTGCAGTGCAGTGG TTTTTTCTTTTTTTTTTTGAGATGGGGTCTCAGTCTGTCTCCCAGGCTGCAGTGCAGTGCAGTGG T C SRSF4 Ensembl:ENSG00000116350 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr1:29174178..29174179 24183664,29129909 RNA-Seq:(High) rs928745930 Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_96143,Human_RBP_ID_5807531,Human_RBP_ID_10923843,Human_RBP_ID_17557068 RMVar_hsa_circ_122894,RMVar_hsa_circ_130943 52370 RMVar_ID_52370 Human_SNP_ID_802919084 A-to-I Human chr1 + 111459455 111459455 111459455 AAACAATATTTATCATTTCTTAATTTTGCCCCAGAATAACATTGCTATGGCTTTGGAAGTTACTT AAACAATATTTATCATTTCTTAATTTTGCCCCTGAATAACATTGCTATGGCTTTGGAAGTTACTT A T ATP5PB Ensembl:ENSG00000116459 Protein coding intron GSE105773 Glioblastoma cells,U87MG chr1:111459454..111459455 29724793 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 3 liver Human_RBP_ID_858447 RMVar_hsa_circ_135294,RMVar_hsa_circ_291545,RMVar_hsa_circ_135297,RMVar_hsa_circ_135298,RMVar_hsa_circ_108654 52371 RMVar_ID_52371 Human_SNP_ID_802974177 A-to-I Human chr1 - 1094490 1094490 1094490 AGGCTGAGGCAGGAGAATGGTGTGAACCCAGAAGGCGGGGCTTGCAGTGAACTGAGATCACGCCA AGGCTGAGGCAGGAGAATGGTGTGAACCCAGACGGCGGGGCTTGCAGTGAACTGAGATCACGCCA T G C1orf159 Ensembl:ENSG00000131591 Protein coding intron GSE100210 HepG2 cell line chr1:1094489..1094490 29129909 RNA-Seq:(High) rs981920110 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_22557438,Human_RBP_ID_22706772 52372 RMVar_ID_52372 Human_SNP_ID_802995148 A-to-I Human chr1 + 28572385 28572385 28572385 CCAGCTAATTATTTTGTATTTTTAGTAGAGACAGGGTTTCTCCATGTTGGCTTGGCCGGTCTCAA CCAGCTAATTATTTTGTATTTTTAGTAGAGACGGGGTTTCTCCATGTTGGCTTGGCCGGTCTCAA A G TRNAU1AP Ensembl:ENSG00000180098 Protein coding intron GSE100210 HepG2 cell line chr1:28572384..28572385 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_10918228 RMVar_hsa_circ_37958 52373 RMVar_ID_52373 Human_SNP_ID_803006961 A-to-I Human chr1 - 202331812 202331812 202331812 TGATGTTTAGGGGACTTGTCCTGGTTCATCTTAGTTAATGTGTTCTTTGCCAAGGTGATCTAAGT TGATGTTTAGGGGACTTGTCCTGGTTCATCTTGGTTAATGTGTTCTTTGCCAAGGTGATCTAAGT T C UBE2T Ensembl:ENSG00000077152 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector chr1:202331811..202331812 29967493 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC 33..33 33 PAAD 2 - Human_RBP_ID_272215,Human_RBP_ID_337833,Human_RBP_ID_973866,Human_RBP_ID_1346132,Human_RBP_ID_1418741,Human_RBP_ID_1733309,Human_RBP_ID_2115675,Human_RBP_ID_3292570,Human_RBP_ID_8295130,Human_RBP_ID_8961161,Human_RBP_ID_10727334,Human_RBP_ID_17646184,Human_RBP_ID_18560000,Human_RBP_ID_23205514,Human_RBP_ID_23355905,Human_RBP_ID_26850158 RMVar_hsa_circ_82340,RMVar_hsa_circ_118498,RMVar_hsa_circ_127172,RMVar_hsa_circ_96725,RMVar_hsa_circ_138918,RMVar_hsa_circ_138920,RMVar_hsa_circ_138921,RMVar_hsa_circ_138919 52374 RMVar_ID_52374 Human_SNP_ID_803047962 A-to-I Human chr1 - 206696095 206696095 206696095 CTGGCAAAGAAATCATCTGCCGTGTGACTGGTAGGATGAAGGTGAAGGCAGGTGAGATGAATCCT CTGGCAAAGAAATCATCTGCCGTGTGACTGGTGGGATGAAGGTGAAGGCAGGTGAGATGAATCCT T C AL591846.2 Ensembl:ENSG00000224114 Pseudogene exon GSE100210 HepG2 cell line chr1:206696094..206696095 29129909 RNA-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 52375 RMVar_ID_52375 Human_SNP_ID_803055782 A-to-I Human chr1 + 171762386 171762386 171762386 TCACAGCTACTCTAGAGGTGGTGGGAACCAGGACTATGGGAGTGGCAGGTATGACAGTTGACCTG TCACAGCTACTCTAGAGGTGGTGGGAACCAGGGCTATGGGAGTGGCAGGTATGACAGTTGACCTG A G Z98751.2 Ensembl:ENSG00000236741 Pseudogene exon GSE100210 HepG2 cell line chr1:171762385..171762386 29129909 RNA-Seq:(High) rs1209178334 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_5890114,Human_RBP_ID_8241454 52376 RMVar_ID_52376 Human_SNP_ID_803109761 A-to-I Human chr1 - 57135378 57135378 57135378 ATGAGCCTTGAAGACATTATGCTGAGTGAATTAAGCCAGGCACAAAAAGACAAATATTGTATGAT ATGAGCCTTGAAGACATTATGCTGAGTGAATTGAGCCAGGCACAAAAAGACAAATATTGTATGAT T C DAB1 Ensembl:ENSG00000173406 Protein coding intron GSE107867 ASD brains,cerebellum chr1:57135377..57135378 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - RMVar_hsa_circ_16433,RMVar_hsa_circ_302283,RMVar_hsa_circ_331671,RMVar_hsa_circ_350191,RMVar_hsa_circ_133292,RMVar_hsa_circ_50573 52377 RMVar_ID_52377 Human_SNP_ID_803116792 A-to-I Human chr1 - 72179393 72179393 72179393 AACAAATAACTGCAGAATCTCAATAACATTCAAAACAGCATGGTATTGGAACAAAACCAGACACA AACAAATAACTGCAGAATCTCAATAACATTCACAACAGCATGGTATTGGAACAAAACCAGACACA T G NEGR1 Ensembl:ENSG00000172260 Protein coding intron GSE107867 ASD brains,frontal_cortex chr1:72179392..72179393 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 2 - 52378 RMVar_ID_52378 Human_SNP_ID_803143716 A-to-I Human chr1 + 179543277 179543276 179543277 TTAGCAAATCACTGTGCTCTGAGCTGTGACTGAAAAAGGAATCAAGAGGGAAGTTTGCAAAGATG TTAGCAAATCACTGTGCTCTGAGCTGTGACTG_AAAAGGAATCAAGAGGGAAGTTTGCAAAGATG GA G AXDND1 Ensembl:ENSG00000162779 Protein coding intron GSE47997 K562 cells&HepG2 cells chr1:179543276..179543277;chr1:179543277..179543278 23474544 RNA-Seq:(High) - Functional Loss DEL ICGC 33..33 33 LICA 1 - 52379 RMVar_ID_52379 Human_SNP_ID_803149573 A-to-I Human chr1 + 944260 944260 944260 CGCTTTATTTCTTTCGGTTTCGGATGCAAAACAAAAAATTTTAAAAGAAAATGTGACTTCAAAGG CGCTTTATTTCTTTCGGTTTCGGATGCAAAACGAAAAATTTTAAAAGAAAATGTGACTTCAAAGG A G SAMD11 Ensembl:ENSG00000187634 Protein coding 3'UTR GSE100210 HepG2 cell line chr1:944260..944261 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 CHOL 1 - Human_RBP_ID_1755683,Human_RBP_ID_8050535,Human_RBP_ID_18582310,Human_RBP_ID_22147822,Human_RBP_ID_22869132 RMVar_hsa_circ_117918,RMVar_hsa_circ_128235 52380 RMVar_ID_52380 Human_SNP_ID_803168984 A-to-I Human chr1 - 165663025 165663025 165663025 CTTTTTGAAAACCTGCAGTGAAACCTATTGACATGGCCACGCTGTGGAATGATGTGAATTGGCCC CTTTTTGAAAACCTGCAGTGAAACCTATTGACTTGGCCACGCTGTGGAATGATGTGAATTGGCCC T A ALDH9A1 Ensembl:ENSG00000143149 Protein coding 3'UTR GSE100210 HepG2 cell line chr1:165663024..165663025 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_331120,Human_RBP_ID_972385,Human_RBP_ID_4084172,Human_RBP_ID_8288980,Human_RBP_ID_23205416,Human_RBP_ID_23341162 Human_miRNA_ID_215379,Human_miRNA_ID_877063,Human_miRNA_ID_2392191,Human_miRNA_ID_2564437 RMVar_hsa_circ_82595,RMVar_hsa_circ_87668,RMVar_hsa_circ_137275,RMVar_hsa_circ_137276 52381 RMVar_ID_52381 Human_SNP_ID_803222396 A-to-I Human chr1 - 208963573 208963573 208963573 TAAAACTAGATCCCTAATCTCACCGTATACAAAAATCAACTCAAAATAGATTAAAGACAAACGTA TAAAACTAGATCCCTAATCTCACCGTATACAAGAATCAACTCAAAATAGATTAAAGACAAACGTA T C - - Other Unknown GSE100210 HepG2 cell line chr1:208963572..208963573 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 52382 RMVar_ID_52382 Human_SNP_ID_803222588 A-to-I Human chr1 + 78750087 78750087 78750087 CTGGGATCAAAACTCATGTGGAAAAAGAGGATAGGGAGGCACGTGAGAGGAATGAAATCCGGCAT CTGGGATCAAAACTCATGTGGAAAAAGAGGATGGGGAGGCACGTGAGAGGAATGAAATCCGGCAT A G AC104837.1 Ensembl:ENSG00000235400 Pseudogene exon GSE100210 HepG2 cell line chr1:78750086..78750087 29129909 RNA-Seq:(High) rs879108768 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_18523749 52383 RMVar_ID_52383 Human_SNP_ID_803222592 A-to-I Human chr1 + 78750087 78750087 78750087 CTGGGATCAAAACTCATGTGGAAAAAGAGGATAGGGAGGCACGTGAGAGGAATGAAATCCGGCAT CTGGGATCAAAACTCATGTGGAAAAAGAGGATTGGGAGGCACGTGAGAGGAATGAAATCCGGCAT A T AC104837.1 Ensembl:ENSG00000235400 Pseudogene exon GSE100210 HepG2 cell line chr1:78750086..78750087 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 RECA 1 - Human_RBP_ID_18523749 52384 RMVar_ID_52384 Human_SNP_ID_803255224 A-to-I Human chr1 + 87046410 87046410 87046410 AGAGCTGACCCTGAAGCTGCCTGGGAACCAACAGAAGCCAAAGCCAGAGCTAGAACATTCTAATA AGAGCTGACCCTGAAGCTGCCTGGGAACCAACGGAAGCCAAAGCCAGAGCTAGAACATTCTAATA A G AC093155.1,HS2ST1,AC093155.3 Ensembl:ENSG00000225568,Ensembl:ENSG00000153936,Ensembl:ENSG00000267561 Pseudogene,Protein coding,Protein coding exon,intron,intron GSE100210 HepG2 cell line chr1:87046409..87046410 29129909 RNA-Seq:(High) rs879023928 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 8 haematopoietic and lymphoid tissue Human_RBP_ID_5889943,Human_RBP_ID_8242589,Human_RBP_ID_17340033,Human_RBP_ID_17456709,Human_RBP_ID_17586671,Human_RBP_ID_26383775 52385 RMVar_ID_52385 Human_SNP_ID_803258349 A-to-I Human chr1 - 155905965 155905965 155905965 AATTAGCCGGGCAATAGTGGCATGTGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAA AATTAGCCGGGCAATAGTGGCATGTGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAA T C RIT1 Ensembl:ENSG00000143622 Protein coding intron GSE38233 cultured B-cells chr1:155905964..155905965 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_81183,RMVar_hsa_circ_136724 52386 RMVar_ID_52386 Human_SNP_ID_803271775 A-to-I Human chr1 + 58723081 58723081 58723081 AGTCAGCTCAGGCTGCTATGACAAGATACCACAGACTGGGTGGCTTAAACAACAGACTTACTTCT AGTCAGCTCAGGCTGCTATGACAAGATACCACTGACTGGGTGGCTTAAACAACAGACTTACTTCT A T AL136985.3 Ensembl:ENSG00000283445 lincRNA intron GSE100210 HepG2 cell line chr1:58723080..58723081 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 52387 RMVar_ID_52387 Human_SNP_ID_803286454 A-to-I Human chr1 - 52917056 52917056 52917056 ACCACGCCTGGCTAATTTTTGTCTTTTTAGTAAAGACGGGGTTTCACCATGTTGGTCAGGCTGGT ACCACGCCTGGCTAATTTTTGTCTTTTTAGTAGAGACGGGGTTTCACCATGTTGGTCAGGCTGGT T C ECHDC2 Ensembl:ENSG00000121310 Protein coding intron GSE47997 K562 cells&HepG2 cells chr1:52917055..52917056 23474544 RNA-Seq:(High) rs995547843 Functional Loss SNV ICGC 33..33 33 PRAD 1 - 52388 RMVar_ID_52388 Human_SNP_ID_803314420 A-to-I Human chr1 - 150613254 150613252 150613254 CAAATAGTTTTTTGTTTGTTTGTTTTAGACAGAGTGTTGCTCTTGTTTCCCAGGCTGGAGAGCAA CAAATAGTTTTTTGTTTGTTTGTTTTAGACAG__TGTTGCTCTTGTTTCCCAGGCTGGAGAGCAA ACT A ENSA Ensembl:ENSG00000143420 Protein coding intron GSE100210 HepG2 cell line chr1:150613253..150613254 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 33..34 33 LICA 1 - Human_RBP_ID_5687522 52389 RMVar_ID_52389 Human_SNP_ID_803343393 A-to-I Human chr1 - 25229077 25229077 25229077 ATTAAATCACCAGGAAGTTGTGGAAGAAGATAAAAGACTAAAATTACCTGCAAATTGGGAAGCCA ATTAAATCACCAGGAAGTTGTGGAAGAAGATACAAGACTAAAATTACCTGCAAATTGGGAAGCCA T G SYF2 Ensembl:ENSG00000117614 Protein coding CDS GSE100210 HepG2 cell line chr1:25229076..25229077 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - 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 52390 RMVar_ID_52390 Human_SNP_ID_803353354 A-to-I Human chr1 - 37500932 37500932 37500932 ATACCTGTTTCCATGCCTCCTAGAAGTTCCGAAGCCAGGGTAAGAGTTCTCATTCTAGAAACTGT ATACCTGTTTCCATGCCTCCTAGAAGTTCCGAGGCCAGGGTAAGAGTTCTCATTCTAGAAACTGT T C MEAF6 Ensembl:ENSG00000163875 Protein coding intron GSE100210 HepG2 cell line chr1:37500931..37500932 29129909 RNA-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_5158781 52391 RMVar_ID_52391 Human_SNP_ID_803355641 A-to-I Human chr1 - 15807419 15807419 15807419 TGCACGGAGGAGCTCTTTGACTTCTTGCATGCAAAGGACCATTGCGTGGCCCACAAACTCTTTAA TGCACGGAGGAGCTCTTTGACTTCTTGCATGCGAAGGACCATTGCGTGGCCCACAAACTCTTTAA T C UQCRHL Ensembl:ENSG00000233954 Protein coding CDS GSE100210 HepG2 cell line chr1:15807418..15807419 29129909 RNA-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 52392 RMVar_ID_52392 Human_SNP_ID_803356546 A-to-I Human chr1 + 117082237 117082237 117082237 TAAGCATAATAATAATTCTTATTTTTTGAGACAGGGTCTCGCTCTGTTGCTCAGGCTGGAGTGCA TAAGCATAATAATAATTCTTATTTTTTGAGACGGGGTCTCGCTCTGTTGCTCAGGCTGGAGTGCA A G TTF2 Ensembl:ENSG00000116830 Protein coding intron GSE100210 HepG2 cell line chr1:117082236..117082237 29129909 RNA-Seq:(High) rs200199061 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_miRNA_ID_1949954,Human_miRNA_ID_1951238,Human_miRNA_ID_2443323 RMVar_hsa_circ_116031,RMVar_hsa_circ_119088,RMVar_hsa_circ_96197,RMVar_hsa_circ_135648,RMVar_hsa_circ_135649,RMVar_hsa_circ_135651,RMVar_hsa_circ_92212,RMVar_hsa_circ_135654,RMVar_hsa_circ_101578,RMVar_hsa_circ_110065,RMVar_hsa_circ_135652,RMVar_hsa_circ_80085,RMVar_hsa_circ_135655,RMVar_hsa_circ_126216,RMVar_hsa_circ_135653,RMVar_hsa_circ_120763,RMVar_hsa_circ_135656,RMVar_hsa_circ_110780,RMVar_hsa_circ_93760,RMVar_hsa_circ_135658,RMVar_hsa_circ_98395,RMVar_hsa_circ_135659,RMVar_hsa_circ_135660,RMVar_hsa_circ_78374,RMVar_hsa_circ_88077,RMVar_hsa_circ_135661,RMVar_hsa_circ_135662,RMVar_hsa_circ_135663 52393 RMVar_ID_52393 Human_SNP_ID_803412763 A-to-I Human chr1 + 97546696 97546696 97546696 ACATTAATATCCATGCCATATCATGTGTGTACACTAAAAGATACAGAGGAAGTAGAGCTGAAGTT ACATTAATATCCATGCCATATCATGTGTGTACGCTAAAAGATACAGAGGAAGTAGAGCTGAAGTT A G SEC63P1 Ensembl:ENSG00000228057 Pseudogene exon GSE100210 HepG2 cell line chr1:97546695..97546696 29129909 RNA-Seq:(High) rs1184123778 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue 52394 RMVar_ID_52394 Human_SNP_ID_803413544 A-to-I Human chr1 - 161526251 161526251 161526251 TTTTTGGCAGCCACTCTGTCCCTCTGGGCCTCATCCTCAGCCTTGTACTGCTCGGCTTCATGAAC TTTTTGGCAGCCACTCTGTCCCTCTGGGCCTCGTCCTCAGCCTTGTACTGCTCGGCTTCATGAAC T C lnc-FCGR3A-2 RNACentral:URS00008BD94B lincRNA intron GSE38233 cultured B-cells chr1:161526251..161526252 24183664 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus 52395 RMVar_ID_52395 Human_SNP_ID_803451955 A-to-I Human chr1 - 28243590 28243590 28243590 AGAAACCCCATCTTCACTAAAAATACAAAATTAGCTGGGCGTGTTGGTGTAATTCCAGCTACTTG AGAAACCCCATCTTCACTAAAAATACAAAATTCGCTGGGCGTGTTGGTGTAATTCCAGCTACTTG T G - - Other Unknown GSE100210 HepG2 cell line chr1:28243589..28243590 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - RMVar_hsa_circ_130823 52396 RMVar_ID_52396 Human_SNP_ID_803586429 A-to-I Human chr1 + 32683901 32683901 32683901 GTGATCCACCCTCCTCAGCCTCCCAAAGTGCTAGGATTACAGGCGTGAGCCACCCCGTCCGGCCT GTGATCCACCCTCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCCCGTCCGGCCT A G RBBP4 Ensembl:ENSG00000162521 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line chr1:32683900..32683901 29129909,31158229,31158229 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 colon adenocarcinoma,LAML,LUSC,large_intestine adenocarcinoma,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 11 large intestine,haematopoietic and lymphoid tissue 52397 RMVar_ID_52397 Human_SNP_ID_803592556 A-to-I Human chr1 - 154209021 154209021 154209021 TCTGAAGGCCAGGCATGGTGGCTCACGGCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGTGG TCTGAAGGCCAGGCATGGTGGCTCACGGCTGTTATCCCAGCACTTTGGGAGGCTGAGGCGGGTGG T A C1orf43 Ensembl:ENSG00000143612 Protein coding intron GSE100210 HepG2 cell line chr1:154209020..154209021 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 6 liver RMVar_hsa_circ_136359,RMVar_hsa_circ_121933 52398 RMVar_ID_52398 Human_SNP_ID_803604557 A-to-I Human chr1 - 205791579 205791579 205791579 GCTTGGCACTGGGCTCCTAGCACTCAGCTTCCATGTTCTCTGGCTCATAGGGGACCGAGACACGG GCTTGGCACTGGGCTCCTAGCACTCAGCTTCCTTGTTCTCTGGCTCATAGGGGACCGAGACACGG T A SLC41A1 Ensembl:ENSG00000133065 Protein coding exon GSE112787 293 Flip-In T-REx cells,empty vector chr1:205791578..205791579 29967493 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 3 lung Human_RBP_ID_10742553,Human_RBP_ID_17215209 RMVar_hsa_circ_80783,RMVar_hsa_circ_139234 52399 RMVar_ID_52399 Human_SNP_ID_803618877 A-to-I Human chr1 + 226067477 226067477 226067477 ATACAGAGAGTGGGCCGGGCGCCGTGACTCACATCTGTAATCCCAACACTTTGGGAGGCTGAGGT ATACAGAGAGTGGGCCGGGCGCCGTGACTCACCTCTGTAATCCCAACACTTTGGGAGGCTGAGGT A C H3-3A Ensembl:ENSG00000163041 Protein coding intron GSE100210 HepG2 cell line chr1:226067476..226067477 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 UTCA,endometrium carcinosarcoma-malignant_mesodermal_mixed_tumour 4 uterus Human_RBP_ID_5768631 RMVar_hsa_circ_77982,RMVar_hsa_circ_140083 52400 RMVar_ID_52400 Human_SNP_ID_803621206 A-to-I Human chr1 - 45656958 45656928 45656958 GTAGAGGCTGGGCTCAGTGGCTCATGCCTGTAATCCCAGCACTTTGAGAGGCTGAGGCAGAAGGA GTAGAGGCTGGGCTCAGTGGCTCATGCCTGTA______________________________GGA CTTCTGCCTCAGCCTCTCAAAGTGCTGGGAT C GPBP1L1 Ensembl:ENSG00000159592 Protein coding intron GSE38233 cultured B-cells chr1:45656957..45656958 24183664 RNA-Seq:(High) - Functional Loss DEL ICGC 33..62 33 PAAD 1 - 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_343973,RMVar_hsa_circ_379075,RMVar_hsa_circ_132564 52401 RMVar_ID_52401 Human_SNP_ID_803637110 A-to-I Human chr1 + 39002475 39002475 39002475 GGTCTAGGCCGGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCAG GGTCTAGGCCGGGCGCAGTGGCTCACGCCTGTTATCCCAGCACTTTGGGAGGCCGAGGCGGGCAG A T AKIRIN1 Ensembl:ENSG00000174574 Protein coding intron GSE38233 cultured B-cells chr1:39002474..39002475 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_16000 52402 RMVar_ID_52402 Human_SNP_ID_803664816 A-to-I Human chr1 - 39546877 39546877 39546877 CTCTTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGTGTGAGACACCCCACCCAACTATATCTAT CTCTTGCCTTGGCCTCCCAAAGTGCTGGGATTGCAGTGTGAGACACCCCACCCAACTATATCTAT T C PPIEL Ensembl:ENSG00000243970 Pseudogene intron GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from NIH NeuroBioBank chr1:39546876..39546877 29129909,30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_5245085,Human_RBP_ID_17341396,Human_RBP_ID_18574607 RMVar_hsa_circ_131955,RMVar_hsa_circ_43307,RMVar_hsa_circ_308231,RMVar_hsa_circ_346767,RMVar_hsa_circ_72011,RMVar_hsa_circ_131956,RMVar_hsa_circ_66998 52403 RMVar_ID_52403 Human_SNP_ID_803669214 A-to-I Human chr1 + 179356923 179356923 179356923 GTTGCCCAGGCTGGTCTCAAACTCTTCACCTCAAGCAAAACTCCCACTGCAGAAAGCTTTGGGAT GTTGCCCAGGCTGGTCTCAAACTCTTCACCTCTAGCAAAACTCCCACTGCAGAAAGCTTTGGGAT A T SOAT1 Ensembl:ENSG00000057252 Protein coding 3'UTR GSE100210 HepG2 cell line chr1:179356923..179356924 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_26386751 RMVar_hsa_circ_264822 52404 RMVar_ID_52404 Human_SNP_ID_803671578 A-to-I Human chr1 + 36042184 36042184 36042184 TTGGCTCACTGCAGCCCCCACCTCCTGGGTTCAAGTGATTGTCAGGCCTCAGCCTCCTGAGTAGC TTGGCTCACTGCAGCCCCCACCTCCTGGGTTCGAGTGATTGTCAGGCCTCAGCCTCCTGAGTAGC A G AGO3 Ensembl:ENSG00000126070 Protein coding intron GSE100210 HepG2 cell line chr1:36042184..36042185 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_10964820 RMVar_hsa_circ_23771,RMVar_hsa_circ_297112,RMVar_hsa_circ_131634,RMVar_hsa_circ_359402,RMVar_hsa_circ_277107,RMVar_hsa_circ_37549,RMVar_hsa_circ_369805,RMVar_hsa_circ_341689,RMVar_hsa_circ_363253,RMVar_hsa_circ_131639,RMVar_hsa_circ_371580,RMVar_hsa_circ_131643,RMVar_hsa_circ_131644,RMVar_hsa_circ_104216,RMVar_hsa_circ_123067,RMVar_hsa_circ_131645,RMVar_hsa_circ_319246,RMVar_hsa_circ_131648,RMVar_hsa_circ_272132,RMVar_hsa_circ_119509,RMVar_hsa_circ_102780,RMVar_hsa_circ_131649,RMVar_hsa_circ_273076,RMVar_hsa_circ_131651,RMVar_hsa_circ_131650,RMVar_hsa_circ_283470,RMVar_hsa_circ_131654,RMVar_hsa_circ_131655,RMVar_hsa_circ_7665,RMVar_hsa_circ_375264,RMVar_hsa_circ_131656 52405 RMVar_ID_52405 Human_SNP_ID_803705748 A-to-I Human chr1 - 240143459 240143459 240143459 AGAAGGAAAAGAAGGACAAGGACAAAAAGGAAACCCCTGCTGACATGGGAGCACATCAGGGAGTG AGAAGGAAAAGAAGGACAAGGACAAAAAGGAAGCCCCTGCTGACATGGGAGCACATCAGGGAGTG T C AL359918.2 Ensembl:ENSG00000228818 Pseudogene exon GSE100210 HepG2 cell line chr1:240143458..240143459 29129909 RNA-Seq:(High) rs878884355 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue Human_miRNA_ID_1840561,Human_miRNA_ID_1841305,Human_miRNA_ID_1862797,Human_miRNA_ID_1908532 52406 RMVar_ID_52406 Human_SNP_ID_803731922 A-to-I Human chr1 + 150308767 150308767 150308767 CTGAGGCAGGAGAATTGCTTGAACTGGGGAGGAAGAGGTTGCAGTGAGCCAAGATCATGCCACTG CTGAGGCAGGAGAATTGCTTGAACTGGGGAGGCAGAGGTTGCAGTGAGCCAAGATCATGCCACTG A C MRPS21 Ensembl:ENSG00000266472 Protein coding 3'UTR GSE99789 esophageal squamous carcinoma cells,EC109 chr1:150308767..150308768 29796672 RNA-Seq:(High) rs580060 Functional Loss SNV ICGC 33..33 33 ESCA 1 - 52407 RMVar_ID_52407 Human_SNP_ID_803745151 A-to-I Human chr1 - 75743996 75743996 75743996 TTTTTAATGAGATTGATGTGAGTAACATCCAGAAGATGAGGGCTCGGCACAAAGAGGCTTTTTTG TTTTTAATGAGATTGATGTGAGTAACATCCAGGAGATGAGGGCTCGGCACAAAGAGGCTTTTTTG T C DLSTP1 Ensembl:ENSG00000181227 Pseudogene exon GSE100210 HepG2 cell line chr1:75743995..75743996 29129909 RNA-Seq:(High) rs954651277 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 5 haematopoietic and lymphoid tissue Human_miRNA_ID_1898130 52408 RMVar_ID_52408 Human_SNP_ID_803755041 A-to-I Human chr1 + 155315562 155315562 155315563 AATATTAGCCGGGCATGGTGGCAGGCGCCTGTAGTCCCAGCTATTTGGGAGGCTGAGGTAGGAGA AATATTAGCCGGGCATGGTGGCAGGCGCCTGTCCTCCCAGCTATTTGGGAGGCTGAGGTAGGAGA AG CC FDPS Ensembl:ENSG00000160752 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr1:155315561..155315562 24183664,29129909 RNA-Seq:(High) - Functional Loss MNV ICGC 33..34 33 MELA 1 - 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 52409 RMVar_ID_52409 Human_SNP_ID_803769396 A-to-I Human chr1 + 228115333 228115333 228115333 TTCTTCTAAAGTATTGGGCTTTTCTGGGTCCCAGATAGTTCGAATCAAATCATAAACCTCTAGCA TTCTTCTAAAGTATTGGGCTTTTCTGGGTCCCGGATAGTTCGAATCAAATCATAAACCTCTAGCA A G lnc-ARF1-3,lnc-ARF1-3:2,lnc-ARF1-3:3 RNACentral:URS0000D5BE25,RNACentral:URS0000D5BE5E,RNACentral:URS00008C1AA8 lincRNA,lincRNA,lincRNA intron,exon,intron GSE100210 HepG2 cell line chr1:228115332..228115333 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 1 - 52410 RMVar_ID_52410 Human_SNP_ID_803883687 A-to-I Human chr1 + 204556543 204556542 204556543 ACATGGTGAAACCCTGTCTCTACCAAAAATACAAAAAAAAAGCTGGGCATGGTGGGTGCATGCTT ACATGGTGAAACCCTGTCTCTACCAAAAATAC_AAAAAAAAGCTGGGCATGGTGGGTGCATGCTT CA C MDM4 Ensembl:ENSG00000198625 Protein coding 3'UTR GSE100210 HepG2 cell line chr1:204556543..204556544 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 33..33 33 BRCA 1 - Human_RBP_ID_10737395,Human_RBP_ID_17736074,Human_RBP_ID_24625344 RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_89387,RMVar_hsa_circ_92157,RMVar_hsa_circ_139148,RMVar_hsa_circ_139153,RMVar_hsa_circ_83671,RMVar_hsa_circ_139156,RMVar_hsa_circ_139157,RMVar_hsa_circ_119956,RMVar_hsa_circ_88043,RMVar_hsa_circ_91682,RMVar_hsa_circ_139158,RMVar_hsa_circ_139159 52411 RMVar_ID_52411 Human_SNP_ID_803889969 A-to-I Human chr1 - 114413519 114413519 114413519 AGTTTCATTCTTGTTGCCCAGGCTGATGTGCAATAGCACGATCTTGACTCACCTTAACCTCTGCC AGTTTCATTCTTGTTGCCCAGGCTGATGTGCAGTAGCACGATCTTGACTCACCTTAACCTCTGCC T C TRIM33 Ensembl:ENSG00000197323 Protein coding intron GSE100210 HepG2 cell line chr1:114413518..114413519 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_5674823,Human_RBP_ID_10533846 RMVar_hsa_circ_74288,RMVar_hsa_circ_135531,RMVar_hsa_circ_112335,RMVar_hsa_circ_135533,RMVar_hsa_circ_135535,RMVar_hsa_circ_75355,RMVar_hsa_circ_116113 52412 RMVar_ID_52412 Human_SNP_ID_803902142 A-to-I Human chr1 - 72173074 72173074 72173074 TGAGTGCAGGAGGTCCAGGCTGCAGTGAGCCAAGACCATGCCACTACACTCCAGCCTGGGTGACA TGAGTGCAGGAGGTCCAGGCTGCAGTGAGCCACGACCATGCCACTACACTCCAGCCTGGGTGACA T G NEGR1 Ensembl:ENSG00000172260 Protein coding intron GSE107867 ASD brains,temporal_cortex chr1:72173073..72173074 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 52413 RMVar_ID_52413 Human_SNP_ID_803950092 A-to-I Human chr1 - 92273594 92273594 92273594 AAAAATAAAAAAAAAATAGCGGGCATGGTGGCATGTACCAGTAGTCCTAGCTACTCAGGAGACTG AAAAATAAAAAAAAAATAGCGGGCATGGTGGCGTGTACCAGTAGTCCTAGCTACTCAGGAGACTG T C GLMN Ensembl:ENSG00000174842 Protein coding intron GSE100210 HepG2 cell line chr1:92273593..92273594 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BOCA 1 - RMVar_hsa_circ_692,RMVar_hsa_circ_349620,RMVar_hsa_circ_292299,RMVar_hsa_circ_134515,RMVar_hsa_circ_134516,RMVar_hsa_circ_37586,RMVar_hsa_circ_304526,RMVar_hsa_circ_32242,RMVar_hsa_circ_134518,RMVar_hsa_circ_985,RMVar_hsa_circ_134522,RMVar_hsa_circ_275426,RMVar_hsa_circ_296044,RMVar_hsa_circ_134523,RMVar_hsa_circ_314222,RMVar_hsa_circ_134521,RMVar_hsa_circ_134524 52414 RMVar_ID_52414 Human_SNP_ID_803981310 A-to-I Human chr1 - 71685390 71685390 71685390 TGAACCCAGGAGGCGGAGTTTGCAGTGAGCCAAGATCATGCCATTGCACTCCAGCCTGGGCAAAA TGAACCCAGGAGGCGGAGTTTGCAGTGAGCCACGATCATGCCATTGCACTCCAGCCTGGGCAAAA T G NEGR1 Ensembl:ENSG00000172260 Protein coding intron GSE47997 K562 cells&HepG2 cells chr1:71685389..71685390 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 3 pancreas RMVar_hsa_circ_15617,RMVar_hsa_circ_334592 52415 RMVar_ID_52415 Human_SNP_ID_803994147 A-to-I Human chr1 + 78750105 78750105 78750105 TGGAAAAAGAGGATAGGGAGGCACGTGAGAGGAATGAAATCCGGCATGACAGGCGAAAAGAGAGA TGGAAAAAGAGGATAGGGAGGCACGTGAGAGGGATGAAATCCGGCATGACAGGCGAAAAGAGAGA A G AC104837.1 Ensembl:ENSG00000235400 Pseudogene exon GSE100210 HepG2 cell line chr1:78750104..78750105 29129909 RNA-Seq:(High) rs879107042 Functional Loss SNV ICGC 33..33 33 LAML 2 - 52416 RMVar_ID_52416 Human_SNP_ID_804004055 A-to-I Human chr1 + 174854817 174854817 174854817 CAGGCTGGAGCGCAGTGATCTTGGCTCACTGTAACCTCTGCCCCCAGGATTCAAGTGATTCTCTT CAGGCTGGAGCGCAGTGATCTTGGCTCACTGTTACCTCTGCCCCCAGGATTCAAGTGATTCTCTT A T RABGAP1L Ensembl:ENSG00000152061 Protein coding intron GSE100210 HepG2 cell line chr1:174854817..174854818 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 6 ovary Human_RBP_ID_10662984 RMVar_hsa_circ_66222 52417 RMVar_ID_52417 Human_SNP_ID_804007768 A-to-I Human chr1 - 19608436 19608436 19608436 GGGCTCTGAGGGCCGACTGGGCCCCAGGTCCAAGGGTCTTGGTCCTATTTCCTCCTGTGGCCCGG GGGCTCTGAGGGCCGACTGGGCCCCAGGTCCAGGGGTCTTGGTCCTATTTCCTCCTGTGGCCCGG T C - - Other Unknown GSE100210 HepG2 cell line chr1:19608435..19608436 29129909 RNA-Seq:(High) rs773953063 Functional Loss SNV ICGC,COSMIC 33..33 33 breast ductal_carcinoma,LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 7 haematopoietic and lymphoid tissue,breast 52418 RMVar_ID_52418 Human_SNP_ID_804025260 A-to-I Human chr1 + 166276832 166276832 166276832 TGAACTCTGCTGCCCGTAGCTGCTGCTCTGTTAGCTATACTGACTTGGAGCTTGGCTGTAGGATC TGAACTCTGCTGCCCGTAGCTGCTGCTCTGTTGGCTATACTGACTTGGAGCTTGGCTGTAGGATC A G AL596087.2 Ensembl:ENSG00000229588 lincRNA intron GSE100210 HepG2 cell line chr1:166276831..166276832 29129909 RNA-Seq:(High) rs879166844 Functional Loss SNV ICGC 33..33 33 ESCA 1 - 52419 RMVar_ID_52419 Human_SNP_ID_804025268 A-to-I Human chr1 - 6648429 6648429 6648429 AATGCTGGTCAGGTGCGGTGGCTCATGCCTGTAATCCCAACACTTTGGGAGGCCAAGGCAGGCGG AATGCTGGTCAGGTGCGGTGGCTCATGCCTGTGATCCCAACACTTTGGGAGGCCAAGGCAGGCGG T C DNAJC11 Ensembl:ENSG00000007923 Protein coding intron GSE100210 HepG2 cell line chr1:6648428..6648429 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_71082,RMVar_hsa_circ_26219 52420 RMVar_ID_52420 Human_SNP_ID_804033858 A-to-I Human chr1 + 153690875 153690875 153690875 TGAGGCAGAAGAATTGCTTGAACCCGGGAGGCAGAGGTTGCGATGAGCCAAGATTACACCACGCA TGAGGCAGAAGAATTGCTTGAACCCGGGAGGCCGAGGTTGCGATGAGCCAAGATTACACCACGCA A C NPR1 Ensembl:ENSG00000169418 Protein coding intron GSE100210 HepG2 cell line chr1:153690874..153690875 29129909 RNA-Seq:(High) rs1359296685 Functional Loss SNV ICGC 33..33 33 LICA 1 - 52421 RMVar_ID_52421 Human_SNP_ID_804047361 A-to-I Human chr1 - 29193224 29193224 29193224 AGAATTACCCAAGGCCTGGCGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAAGCCAAGGC AGAATTACCCAAGGCCTGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAAGCCAAGGC T C MECR Ensembl:ENSG00000116353 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line chr1:29193223..29193224 31158229 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine 52422 RMVar_ID_52422 Human_SNP_ID_804047364 A-to-I Human chr1 - 29193224 29193224 29193224 AGAATTACCCAAGGCCTGGCGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAAGCCAAGGC AGAATTACCCAAGGCCTGGCGCGGTGGCTCACCCCTGTAATCCCAGCACTTTGGGAAGCCAAGGC T G MECR Ensembl:ENSG00000116353 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line chr1:29193223..29193224 31158229 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BLCA 1 - 52423 RMVar_ID_52423 Human_SNP_ID_804077299 A-to-I Human chr1 - 220066106 220066106 220066106 AATTGTATTCATTTTCCACAGAACAATGAAAAACAGCAGTTAAGGGAACACAGGAATGAAGCAAA AATTGTATTCATTTTCCACAGAACAATGAAAAGCAGCAGTTAAGGGAACACAGGAATGAAGCAAA T C BPNT1 Ensembl:ENSG00000162813 Protein coding intron GSE38233 cultured B-cells chr1:220066105..220066106 24183664 RNA-Seq:(High) rs1146773 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 10 haematopoietic and lymphoid tissue Human_Splice_Rec_188902,Human_Splice_Rec_188903 GWAS_ID_5114,GWAS_ID_5115,GWAS_ID_5116,GWAS_ID_5117 RMVar_hsa_circ_71222 52424 RMVar_ID_52424 Human_SNP_ID_804079851 A-to-I Human chr1 + 11950977 11950977 11950977 CACTATGCCCGGCTAATTTTTGTATATTTAGTAGAGATGGGGTATCGCCATGTTGGCCAGGTGGG CACTATGCCCGGCTAATTTTTGTATATTTAGTCGAGATGGGGTATCGCCATGTTGGCCAGGTGGG A C PLOD1 Ensembl:ENSG00000083444 Protein coding intron GSE100210 HepG2 cell line chr1:11950976..11950977 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 caecum adenocarcinoma,large_intestine adenocarcinoma 1 caecum,large intestine RMVar_hsa_circ_81636,RMVar_hsa_circ_77725,RMVar_hsa_circ_126101,RMVar_hsa_circ_129208,RMVar_hsa_circ_129209,RMVar_hsa_circ_79810,RMVar_hsa_circ_129213,RMVar_hsa_circ_116444,RMVar_hsa_circ_321579,RMVar_hsa_circ_129211,RMVar_hsa_circ_369971,RMVar_hsa_circ_51409,RMVar_hsa_circ_101170,RMVar_hsa_circ_129214,RMVar_hsa_circ_129215,RMVar_hsa_circ_122162,RMVar_hsa_circ_92214,RMVar_hsa_circ_112486,RMVar_hsa_circ_129217,RMVar_hsa_circ_129218,RMVar_hsa_circ_129216,RMVar_hsa_circ_129220,RMVar_hsa_circ_87402,RMVar_hsa_circ_129219 52425 RMVar_ID_52425 Human_SNP_ID_804132420 A-to-I Human chr1 + 171762356 171762356 171762356 AGGAGGTGACTTTGGGGCCCATGGGCGTGGTCACAGCTACTCTAGAGGTGGTGGGAACCAGGACT AGGAGGTGACTTTGGGGCCCATGGGCGTGGTCGCAGCTACTCTAGAGGTGGTGGGAACCAGGACT A G Z98751.2 Ensembl:ENSG00000236741 Pseudogene exon GSE100210 HepG2 cell line chr1:171762355..171762356 29129909 RNA-Seq:(High) rs1189514810 Functional Loss SNV ICGC 33..33 33 LAML 1 - 52426 RMVar_ID_52426 Human_SNP_ID_804149467 A-to-I Human chr1 - 220057921 220057921 220057921 TGTCTGCCTCGGACTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCACCTGGCCTAAACCA TGTCTGCCTCGGACTCCCAAAGTGCTGGGATTGCAGGTGTGAGCCACCGCACCTGGCCTAAACCA T C BPNT1 Ensembl:ENSG00000162813 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line chr1:220057920..220057921 23474544,24183664,29129909,31158229,31158229,32596459,32596459 RNA-Seq:(High) rs879012845 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia,large_intestine adenocarcinoma 12 caecum,large intestine,haematopoietic and lymphoid tissue Human_RBP_ID_341873 Human_miRNA_ID_1398426 52427 RMVar_ID_52427 Human_SNP_ID_804191221 A-to-I Human chr1 - 23871989 23871989 23871989 AGCTGGGACTACAGGCACCCGCCACCACACTCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGT AGCTGGGACTACAGGCACCCGCCACCACACTCGGCTAATTTTTGTATTTTTAGTAGAGATGGGGT T C CNR2 Ensembl:ENSG00000188822 Protein coding 3'UTR GSE38233 cultured B-cells chr1:23871988..23871989 24183664 RNA-Seq:(High) rs2501417 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 52428 RMVar_ID_52428 Human_SNP_ID_804238697 A-to-I Human chr1 + 222715488 222715488 222715488 CCAACACTTTGGGAGGCCAAGGCGGGTGGATCACTTGAGGTCAAGAGTTTGAGACCAGCCTGGCC CCAACACTTTGGGAGGCCAAGGCGGGTGGATCGCTTGAGGTCAAGAGTTTGAGACCAGCCTGGCC A G BROX Ensembl:ENSG00000162819 Protein coding intron GSE47997 K562 cells&HepG2 cells chr1:222715487..222715488 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - RMVar_hsa_circ_65968,RMVar_hsa_circ_330924,RMVar_hsa_circ_286453 52429 RMVar_ID_52429 Human_SNP_ID_804239229 A-to-I Human chr1 + 241892676 241892676 241892676 CATTTTTGTATTTTTAGTAGAGATGGAGTTTCAACATGTTGGCCAGGCTGGTCTCTTAATCTCAG CATTTTTGTATTTTTAGTAGAGATGGAGTTTCTACATGTTGGCCAGGCTGGTCTCTTAATCTCAG A T EXO1 Ensembl:ENSG00000174371 Protein coding intron GSE100210 HepG2 cell line chr1:241892675..241892676;chr1:241892676..241892677 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 52430 RMVar_ID_52430 Human_SNP_ID_804286481 A-to-I Human chr1 - 16618532 16618532 16618532 GCTATTTTACAATGAAAAATAATGCTGCAGAGAGCATTTTTGCACATGTATCGTGGCAGATGTAG GCTATTTTACAATGAAAAATAATGCTGCAGAGGGCATTTTTGCACATGTATCGTGGCAGATGTAG T C CROCCP2 Ensembl:ENSG00000215908 Pseudogene exon GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line chr1:16618531..16618532 32596459 RNA-Seq:(High) rs1050322 Functional Loss SNV ICGC 33..33 33 RECA 1 - Human_RBP_ID_1728831,Human_RBP_ID_3286178,Human_RBP_ID_5890897,Human_RBP_ID_8242513,Human_RBP_ID_10648334,Human_RBP_ID_27581310 52431 RMVar_ID_52431 Human_SNP_ID_804292338 A-to-I Human chr1 + 2393026 2393019 2393027 GACGTGAAGAGAAAGGTGGGAGCCAGACTGTCAATGCTCCCGGACGCCAGGCAGAGGACTTCATC GACGTGAAGAGAAAGGTGGGAGCCAG________TGCTCCCGGACGCCAGGCAGAGGACTTCATC GACTGTCAA G RER1 Ensembl:ENSG00000157916 Protein coding intron GSE38233 cultured B-cells chr1:2393026..2393027 24183664 RNA-Seq:(High) - Functional Loss DEL ICGC 27..34 33 CHOL 3 - Human_RBP_ID_803642,Human_RBP_ID_3332615,Human_RBP_ID_5485706,Human_RBP_ID_5778923,Human_RBP_ID_8051573,Human_RBP_ID_9355362,Human_RBP_ID_10839530,Human_RBP_ID_18409896,Human_RBP_ID_18566404,Human_RBP_ID_22022617,Human_RBP_ID_22706954,Human_RBP_ID_22870722,Human_RBP_ID_23112635,Human_RBP_ID_23117610,Human_RBP_ID_23263252,Human_RBP_ID_24358553,Human_RBP_ID_26310081,Human_RBP_ID_27178091,Human_RBP_ID_27555064,Human_RBP_ID_27835068 RMVar_hsa_circ_114059,RMVar_hsa_circ_128459 52432 RMVar_ID_52432 Human_SNP_ID_804295096 A-to-I Human chr1 + 9982834 9982834 9982834 AAGCTTAAAAGTTTAGTAAAAATCGTCTGGGCACAGTGGCTCACGCCTGTAATCCCAGCACTTTG AAGCTTAAAAGTTTAGTAAAAATCGTCTGGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTTTG A G NMNAT1 Ensembl:ENSG00000173614 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr1:9982833..9982834 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_128854,RMVar_hsa_circ_126635,RMVar_hsa_circ_113775,RMVar_hsa_circ_128856 52433 RMVar_ID_52433 Human_SNP_ID_804355144 A-to-I Human chr1 - 15807417 15807417 15807417 CACGGAGGAGCTCTTTGACTTCTTGCATGCAAAGGACCATTGCGTGGCCCACAAACTCTTTAACA CACGGAGGAGCTCTTTGACTTCTTGCATGCAAGGGACCATTGCGTGGCCCACAAACTCTTTAACA T C UQCRHL Ensembl:ENSG00000233954 Protein coding CDS GSE100210 HepG2 cell line chr1:15807416..15807417 29129909 RNA-Seq:(High) rs570054582 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 Human_RBP_ID_4083642 52434 RMVar_ID_52434 Human_SNP_ID_804367292 A-to-I Human chr1 - 150826016 150826015 150826016 CCAGGTACTCGGGAGGCTGAGGCACGAGAATCACTTGAACCTGGGAGGCAGAGGTTGCTGTGAAC CCAGGTACTCGGGAGGCTGAGGCACGAGAATCCTTTGAACCTGGGAGGCAGAGGTTGCTGTGAAC GT AG ARNT Ensembl:ENSG00000143437 Protein coding intron GSE100210 HepG2 cell line chr1:150826015..150826016 29129909 RNA-Seq:(High) - Functional Loss MNV ICGC 33..34 33 MELA 1 - RMVar_hsa_circ_106973,RMVar_hsa_circ_135939,RMVar_hsa_circ_368934,RMVar_hsa_circ_330599,RMVar_hsa_circ_55700,RMVar_hsa_circ_75265,RMVar_hsa_circ_288189,RMVar_hsa_circ_135943,RMVar_hsa_circ_290315,RMVar_hsa_circ_301368,RMVar_hsa_circ_344445,RMVar_hsa_circ_360755,RMVar_hsa_circ_292504,RMVar_hsa_circ_92823,RMVar_hsa_circ_135945,RMVar_hsa_circ_135947,RMVar_hsa_circ_51901,RMVar_hsa_circ_135948,RMVar_hsa_circ_135946,RMVar_hsa_circ_135944 52435 RMVar_ID_52435 Human_SNP_ID_804417943 A-to-I Human chr1 - 15573196 15573196 15573196 GGAGTGCAATGGCATGATCTCGGTTCATTGCAACCTCCGCCTCCCGAGTTCAATCGATTCTCCTG GGAGTGCAATGGCATGATCTCGGTTCATTGCAGCCTCCGCCTCCCGAGTTCAATCGATTCTCCTG T C AGMAT Ensembl:ENSG00000116771 Protein coding 3'UTR GSE99789 esophageal squamous carcinoma cells,EC109 chr1:15573195..15573196 29796672 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 52436 RMVar_ID_52436 Human_SNP_ID_804461240 A-to-I Human chr1 + 10163082 10163082 10163082 TTTGTTTTTTATTATTATTAATAAATAAAGACAGAGTGTTGATCTGTCGCCTTGGCTGGAGTGCA TTTGTTTTTTATTATTATTAATAAATAAAGACGGAGTGTTGATCTGTCGCCTTGGCTGGAGTGCA A G UBE4B Ensembl:ENSG00000130939 Protein coding intron GSE100210 HepG2 cell line chr1:10163081..10163082 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_23302677 RMVar_hsa_circ_3625,RMVar_hsa_circ_90073,RMVar_hsa_circ_128859,RMVar_hsa_circ_303123,RMVar_hsa_circ_304451,RMVar_hsa_circ_21826,RMVar_hsa_circ_60127,RMVar_hsa_circ_55699,RMVar_hsa_circ_363345,RMVar_hsa_circ_320459,RMVar_hsa_circ_128897 52437 RMVar_ID_52437 Human_SNP_ID_804507247 A-to-I Human chr1 - 246560929 246560929 246560929 TTTTGTATTTTTAGTAGAGACGTGGTTTTACCATGTTGGCCAGACTGGTCTGGAACTCCTGACCT TTTTGTATTTTTAGTAGAGACGTGGTTTTACCGTGTTGGCCAGACTGGTCTGGAACTCCTGACCT T C TFB2M Ensembl:ENSG00000162851 Protein coding intron GSE100210 HepG2 cell line chr1:246560928..246560929 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_13690,RMVar_hsa_circ_19800 52438 RMVar_ID_52438 Human_SNP_ID_804530467 A-to-I Human chr1 - 53237552 53237552 53237552 CTCCTGCCTCAGCCTCCCGAGTAGCTGGAATTATAGGCGCCCACCACCACGCCCGGCTAATTTTG CTCCTGCCTCAGCCTCCCGAGTAGCTGGAATTTTAGGCGCCCACCACCACGCCCGGCTAATTTTG T A MAGOH Ensembl:ENSG00000162385 Protein coding intron GSE100210 HepG2 cell line chr1:53237551..53237552 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 2 kidney 52439 RMVar_ID_52439 Human_SNP_ID_804533831 A-to-I Human chr1 - 1402786 1402786 1402786 TACAGACAGGGTTTCTCCATGTTGGTCAGACTAGTCTCGAACTTCCGACCTCAGGTGACCTGCCT TACAGACAGGGTTTCTCCATGTTGGTCAGACTTGTCTCGAACTTCCGACCTCAGGTGACCTGCCT T A MRPL20 Ensembl:ENSG00000242485 Protein coding intron GSE100210 HepG2 cell line chr1:1402785..1402786 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_10555086 52440 RMVar_ID_52440 Human_SNP_ID_804535678 A-to-I Human chr1 - 174004829 174004829 174004829 CCTTTGCATGTTACTCTGAATGGTAAGACCCTATCTTCCCTGGCAGCTTCCCATTAGCCCGATAG CCTTTGCATGTTACTCTGAATGGTAAGACCCTGTCTTCCCTGGCAGCTTCCCATTAGCCCGATAG T C RC3H1 Ensembl:ENSG00000135870 Protein coding intron GSE100210 HepG2 cell line chr1:174004828..174004829 29129909 RNA-Seq:(High) rs959907065 Functional Loss SNV ICGC 33..33 33 RECA 1 - Human_RBP_ID_24608367 52441 RMVar_ID_52441 Human_SNP_ID_804540799 A-to-I Human chr1 + 160895764 160895764 160895764 CTAATAGAAGACTGTATCCCGGTACTGAAGAGATACACCAAAGAAGGGAGAGAATTTGATTATGT CTAATAGAAGACTGTATCCCGGTACTGAAGAGGTACACCAAAGAAGGGAGAGAATTTGATTATGT A G AL354714.2 Ensembl:ENSG00000213080 Pseudogene exon GSE100210 HepG2 cell line chr1:160895763..160895764 29129909 RNA-Seq:(High) rs878870680 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_miRNA_ID_1911248 52442 RMVar_ID_52442 Human_SNP_ID_804548137 A-to-I Human chr1 - 84244406 84244406 84244406 TCCCTCTTTCTCCTCCACATGCTCCTTGATTCACTCCACCTTGTCTGTAGGTTCAATATCAATCT TCCCTCTTTCTCCTCCACATGCTCCTTGATTCGCTCCACCTTGTCTGTAGGTTCAATATCAATCT T C - - Other Unknown GSE100210 HepG2 cell line chr1:84244405..84244406 29129909 RNA-Seq:(High) rs879060353 Functional Loss SNV ICGC 33..33 33 LAML 1 - 52443 RMVar_ID_52443 Human_SNP_ID_804552330 A-to-I Human chr1 + 28510400 28510400 28510400 TGGCTCACACCCGTAATCCCAGCACTTAGGCTAAGGCAGGCGGATCACAACATCTAGAGATCCTG TGGCTCACACCCGTAATCCCAGCACTTAGGCTGAGGCAGGCGGATCACAACATCTAGAGATCCTG A G RCC1,SNHG3 Ensembl:ENSG00000180198,Ensembl:ENSG00000242125 Protein coding,lincRNA intron,exon GSE38233;GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line chr1:28510399..28510400 24183664,29129909,31158229,31158229,32596459 RNA-Seq:(High) rs1047129388 Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 3 breast Human_RBP_ID_8243708,Human_RBP_ID_10916641 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 52444 RMVar_ID_52444 Human_SNP_ID_804563286 A-to-I Human chr1 - 20755347 20755347 20755347 GGCTACTCTTGAACTCCTGGGTTCAGTGAAGTAGTCTGCCTGCCTCAGCTTCCCAAAGTGTTGGA GGCTACTCTTGAACTCCTGGGTTCAGTGAAGTGGTCTGCCTGCCTCAGCTTCCCAAAGTGTTGGA T C HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE38233;GSE100210;GSE99789 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 chr1:20755346..20755347 24183664,29129909,29796672 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue Human_RBP_ID_340133,Human_RBP_ID_10748953,Human_RBP_ID_17557009 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_121886,RMVar_hsa_circ_34502,RMVar_hsa_circ_129887,RMVar_hsa_circ_129888,RMVar_hsa_circ_89876,RMVar_hsa_circ_120042,RMVar_hsa_circ_129890,RMVar_hsa_circ_129891 52445 RMVar_ID_52445 Human_SNP_ID_804572612 A-to-I Human chr1 - 217603802 217603802 217603802 CCTGGCCAACATGGTGAAGCCCCGTCTCTACTAAAAATACAAAAATTAGCAGGGCATGGTGATAT CCTGGCCAACATGGTGAAGCCCCGTCTCTACTCAAAATACAAAAATTAGCAGGGCATGGTGATAT T G GPATCH2 Ensembl:ENSG00000092978 Protein coding intron GSE100210 HepG2 cell line chr1:217603801..217603802 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - RMVar_hsa_circ_110936,RMVar_hsa_circ_76851,RMVar_hsa_circ_139613,RMVar_hsa_circ_119353,RMVar_hsa_circ_139614,RMVar_hsa_circ_139615 52446 RMVar_ID_52446 Human_SNP_ID_804588712 A-to-I Human chr1 - 151455007 151455007 151455007 CGCCTCCTGGGTTCAAGCGATTCTCCTCCTTCAGCTTCCTCAGTAGCTGGGATTACAGGCACGCG CGCCTCCTGGGTTCAAGCGATTCTCCTCCTTCGGCTTCCTCAGTAGCTGGGATTACAGGCACGCG T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE107867 ASD brains,cerebellum chr1:151455006..151455007 30559470 RNA-Seq:(High) rs1290239027 Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 6 ovary Human_Splice_Rec_130067,Human_Splice_Rec_130081 52447 RMVar_ID_52447 Human_SNP_ID_804594351 A-to-I Human chr1 + 38883014 38883014 38883014 AAAATATCTAATTAGAGGCTGGGCTCATGTCTATAATCCTAGCACTTTGGGAGGAGGCTGAGACA AAAATATCTAATTAGAGGCTGGGCTCATGTCTGTAATCCTAGCACTTTGGGAGGAGGCTGAGACA A G AL139260.1 Ensembl:ENSG00000228436 lincRNA intron GSE100210 HepG2 cell line chr1:38883013..38883014 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 52448 RMVar_ID_52448 Human_SNP_ID_804638529 A-to-I Human chr1 + 93458313 93458313 93458313 CATGCAGAAGAATGAATTTTTTGTTTTTAGATAGAGATGGGGTCTTACTGTGTTGCCCATGCTGG CATGCAGAAGAATGAATTTTTTGTTTTTAGATGGAGATGGGGTCTTACTGTGTTGCCCATGCTGG A G FNBP1L Ensembl:ENSG00000137942 Protein coding intron GSE100210 HepG2 cell line chr1:93458312..93458313 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - 52449 RMVar_ID_52449 Human_SNP_ID_804639377 A-to-I Human chr1 + 151205309 151205309 151205309 GCGATTCTCCTGCCTCAGCCTCCTAGGTCACTAGGATCACAGGCGTGCGCCACCACGCCCAGATA GCGATTCTCCTGCCTCAGCCTCCTAGGTCACTGGGATCACAGGCGTGCGCCACCACGCCCAGATA A G PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr1:151205308..151205309 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 52450 RMVar_ID_52450 Human_SNP_ID_804640900 A-to-I Human chr1 + 113450315 113450315 113450315 GGTGGATCTGGCAATTTTATGGGTCGCGGAGGAAACTTTGGAGGTGGTGGAGGAGCTATGGTGGT GGTGGATCTGGCAATTTTATGGGTCGCGGAGGGAACTTTGGAGGTGGTGGAGGAGCTATGGTGGT A G MAGI3,AL391058.1 Ensembl:ENSG00000081026,Ensembl:ENSG00000232499 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line chr1:113450314..113450315 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 10 haematopoietic and lymphoid tissue Human_RBP_ID_800774,Human_RBP_ID_3334165,Human_RBP_ID_8171289,Human_RBP_ID_17104169,Human_RBP_ID_21963670 Human_miRNA_ID_1823860,Human_miRNA_ID_2014595 RMVar_hsa_circ_124622,RMVar_hsa_circ_110517,RMVar_hsa_circ_117193,RMVar_hsa_circ_135438,RMVar_hsa_circ_135439,RMVar_hsa_circ_135440 52451 RMVar_ID_52451 Human_SNP_ID_804653067 A-to-I Human chr1 - 6193612 6193612 6193612 ACCCCTTCTCTTAAAAATGTTAAGCCAGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGG ACCCCTTCTCTTAAAAATGTTAAGCCAGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGG T C RPL22,AL031847.2 Ensembl:ENSG00000116251,Ensembl:ENSG00000285629 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells chr1:6193611..6193612 24183664 RNA-Seq:(High) rs796319218 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 6 brain RMVar_hsa_circ_300295,RMVar_hsa_circ_337176 52452 RMVar_ID_52452 Human_SNP_ID_804656434 A-to-I Human chr1 + 161227956 161227956 161227956 AGTATCGGGGAGATGACTACACAGCCACTCTGACCCTAGGAAATCCTGACCTGATTGGGGAGTCG AGTATCGGGGAGATGACTACACAGCCACTCTGGCCCTAGGAAATCCTGACCTGATTGGGGAGTCG A G TOMM40L Ensembl:ENSG00000158882 Protein coding CDS GSE100210 HepG2 cell line chr1:161227955..161227956 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 3 kidney Human_RBP_ID_18966188,Human_RBP_ID_27390149 Human_Splice_Rec_150646,Human_Splice_Rec_150647,Human_Splice_Rec_150658,Human_Splice_Rec_150659,Human_Splice_Rec_150676,Human_Splice_Rec_150677,Human_Splice_Rec_150694,Human_Splice_Rec_150695,Human_Splice_Rec_150708,Human_Splice_Rec_150709,Human_Splice_Rec_150716,Human_Splice_Rec_150717,Human_Splice_Rec_150732,Human_Splice_Rec_150733,Human_Splice_Rec_150741 Human_miRNA_ID_1188101,Human_miRNA_ID_2377249,Human_miRNA_ID_2568836,Human_miRNA_ID_3092325 RMVar_hsa_circ_137153,RMVar_hsa_circ_372523 52453 RMVar_ID_52453 Human_SNP_ID_804678956 A-to-I Human chr1 + 151237496 151237496 151237496 CAGCCTGAGCATCATGATGAGACCTCATCACTACAAAAACTCAAAAATTACCTGAGTGTGATGGT CAGCCTGAGCATCATGATGAGACCTCATCACTGCAAAAACTCAAAAATTACCTGAGTGTGATGGT A G PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE38233 cultured B-cells chr1:151237495..151237496 24183664 RNA-Seq:(High) rs1223691434 Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 5 breast Human_RBP_ID_17725544 RMVar_hsa_circ_136062,RMVar_hsa_circ_94058,RMVar_hsa_circ_293693,RMVar_hsa_circ_63943,RMVar_hsa_circ_370410,RMVar_hsa_circ_136061,RMVar_hsa_circ_136071,RMVar_hsa_circ_92230,RMVar_hsa_circ_136072,RMVar_hsa_circ_136078,RMVar_hsa_circ_374067,RMVar_hsa_circ_285611,RMVar_hsa_circ_136079 52454 RMVar_ID_52454 Human_SNP_ID_804689127 A-to-I Human chr1 - 150607366 150607366 150607366 GGGAGGCTGAGGTAGGAGAATTGCTTGAACCCAGGAGGCAGGAGGTTGCAGTGAGCTGAGATTGT GGGAGGCTGAGGTAGGAGAATTGCTTGAACCCTGGAGGCAGGAGGTTGCAGTGAGCTGAGATTGT T A ENSA Ensembl:ENSG00000143420 Protein coding intron GSE100210 HepG2 cell line chr1:150607365..150607366 29129909 RNA-Seq:(High) rs1426315338 Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_24584972 52455 RMVar_ID_52455 Human_SNP_ID_804706385 A-to-I Human chr1 + 39459245 39459245 39459245 AAGGAAACTGAATGATGCCTTGGATCGGCTGGAGGAGGTAATGCCCTGCTGAGTGGCCTTCCCTG AAGGAAACTGAATGATGCCTTGGATCGGCTGGGGGAGGTAATGCCCTGCTGAGTGGCCTTCCCTG A G MACF1 Ensembl:ENSG00000127603 Protein coding CDS GSE100210 HepG2 cell line chr1:39459244..39459245 29129909 RNA-Seq:(High) rs761682994 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_96841,Human_RBP_ID_803749,Human_RBP_ID_851454,Human_RBP_ID_8749188,Human_RBP_ID_18968059,Human_RBP_ID_22636798,Human_RBP_ID_22870828,Human_RBP_ID_26314048 Human_Splice_Rec_50001,Human_Splice_Rec_50199,Human_Splice_Rec_50383,Human_Splice_Rec_50715,Human_Splice_Rec_50927,Human_Splice_Rec_51293,Human_Splice_Rec_51423,Human_Splice_Rec_51475,Human_Splice_Rec_51493,Human_Splice_Rec_51499 Human_miRNA_ID_2972064,Human_miRNA_ID_3005247 RMVar_hsa_circ_96358,RMVar_hsa_circ_131901,RMVar_hsa_circ_365402,RMVar_hsa_circ_96246,RMVar_hsa_circ_131928,RMVar_hsa_circ_266362,RMVar_hsa_circ_342077,RMVar_hsa_circ_26390,RMVar_hsa_circ_131947,RMVar_hsa_circ_345730,RMVar_hsa_circ_131949,RMVar_hsa_circ_300611,RMVar_hsa_circ_321086,RMVar_hsa_circ_371541,RMVar_hsa_circ_306498,RMVar_hsa_circ_131948,RMVar_hsa_circ_36727,RMVar_hsa_circ_131946,RMVar_hsa_circ_288567,RMVar_hsa_circ_72309,RMVar_hsa_circ_24314,RMVar_hsa_circ_47065,RMVar_hsa_circ_336690,RMVar_hsa_circ_346179,RMVar_hsa_circ_301746,RMVar_hsa_circ_131951 52456 RMVar_ID_52456 Human_SNP_ID_804713202 A-to-I Human chr1 - 53937281 53937281 53937281 AACTCTGTCTCTATTAAAAATACCAAAAAATTAGTCAGTTGTGGTGGCGTGCACCTATAGTCCCA AACTCTGTCTCTATTAAAAATACCAAAAAATTTGTCAGTTGTGGTGGCGTGCACCTATAGTCCCA T A HSPB11 Ensembl:ENSG00000081870 Protein coding intron GSE100210 HepG2 cell line chr1:53937280..53937281 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_133157,RMVar_hsa_circ_117783,RMVar_hsa_circ_133158,RMVar_hsa_circ_344604,RMVar_hsa_circ_133159 52457 RMVar_ID_52457 Human_SNP_ID_804765929 A-to-I Human chr1 - 225423954 225423954 225423954 CGACAGCACCTCCCAGCTTTACACTGTGAAGTATAAAGATGGAACAGAGCTTGAATTGAAAGAGA CGACAGCACCTCCCAGCTTTACACTGTGAAGTGTAAAGATGGAACAGAGCTTGAATTGAAAGAGA T C LBR Ensembl:ENSG00000143815 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector chr1:225423953..225423954 29967493 RNA-Seq:(High) rs1320764205 Functional Loss SNV TCGA 33..33 33 READ 1 - Human_RBP_ID_1422115,Human_RBP_ID_1738268,Human_RBP_ID_4027705,Human_RBP_ID_5766532,Human_RBP_ID_9491756,Human_RBP_ID_22855889,Human_RBP_ID_26854561,Human_RBP_ID_27176487 Human_Splice_Rec_192453,Human_Splice_Rec_192479,Human_Splice_Rec_192505,Human_Splice_Rec_192541 RMVar_hsa_circ_118468,RMVar_hsa_circ_140023,RMVar_hsa_circ_127091,RMVar_hsa_circ_140034,RMVar_hsa_circ_87052,RMVar_hsa_circ_140035,RMVar_hsa_circ_352875 52458 RMVar_ID_52458 Human_SNP_ID_804775841 A-to-I Human chr1 - 220057933 220057933 220057933 GACATCGTGATCTGTCTGCCTCGGACTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCACC GACATCGTGATCTGTCTGCCTCGGACTCCCAAGGTGCTGGGATTACAGGTGTGAGCCACCGCACC T C BPNT1 Ensembl:ENSG00000162813 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line chr1:220057932..220057933 23474544,24183664,29129909,31158229,31158229 RNA-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 52459 RMVar_ID_52459 Human_SNP_ID_804779050 A-to-I Human chr1 - 10459126 10459126 10459126 CAATAGGCCGGGCGCAGTGGCTCACACCTGTAATCCCAGCATTTTGGGAGGCCAAGGTGGGCGGA CAATAGGCCGGGCGCAGTGGCTCACACCTGTAGTCCCAGCATTTTGGGAGGCCAAGGTGGGCGGA T C DFFA Ensembl:ENSG00000160049 Protein coding 3'UTR GSE38233 cultured B-cells chr1:10459125..10459126 24183664 RNA-Seq:(High) rs1141444 Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 3 oesophagus Human_miRNA_ID_1354831 52460 RMVar_ID_52460 Human_SNP_ID_804803067 A-to-I Human chr1 - 150869088 150869088 150869088 GTCCTGTTGTGTCAGCCAGGCTGGAGTGCAGTAGCGTGACCATAGCTTCCTGCAACACCTCCAAT GTCCTGTTGTGTCAGCCAGGCTGGAGTGCAGTTGCGTGACCATAGCTTCCTGCAACACCTCCAAT T A ARNT Ensembl:ENSG00000143437 Protein coding intron GSE100210 HepG2 cell line chr1:150869087..150869088 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 52461 RMVar_ID_52461 Human_SNP_ID_804821044 A-to-I Human chr1 - 241250968 241250968 241250968 CAATTAAGGACACTTACTGAGCACCAATGCTAAGTGTTAGGGATTTAAAGATGAGCAAGGCATAG CAATTAAGGACACTTACTGAGCACCAATGCTAGGTGTTAGGGATTTAAAGATGAGCAAGGCATAG T C RGS7 Ensembl:ENSG00000182901 Protein coding intron GSE107867 ASD brains,cerebellum chr1:241250967..241250968 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 52462 RMVar_ID_52462 Human_SNP_ID_804897497 A-to-I Human chr1 - 151453209 151453209 151453209 CGCATGCGAAAAGGGAGAAAGAGGCTGGGCGCAGTGGCTCACACCTGTAACCGAAGCACTTTGGG CGCATGCGAAAAGGGAGAAAGAGGCTGGGCGCGGTGGCTCACACCTGTAACCGAAGCACTTTGGG T C POGZ Ensembl:ENSG00000143442 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr1:151453208..151453209 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_10580907 52463 RMVar_ID_52463 Human_SNP_ID_804924513 A-to-I Human chr1 + 112923956 112923956 112923956 GAGGTTCTATGCCTTCAACCCTCTGGCTGGGGACCTGCTGACTGGCAAGTACAAGTATAAGGACA GAGGTTCTATGCCTTCAACCCTCTGGCTGGGGGCCTGCTGACTGGCAAGTACAAGTATAAGGACA A G AKR7A2P1 Ensembl:ENSG00000229020 Pseudogene exon GSE100210 HepG2 cell line chr1:112923955..112923956 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue Human_miRNA_ID_1841270,Human_miRNA_ID_1844521,Human_miRNA_ID_1862762,Human_miRNA_ID_1908497 RMVar_hsa_circ_265530 52464 RMVar_ID_52464 Human_SNP_ID_804936185 A-to-I Human chr1 + 32030326 32030325 32030326 TCAGAAATTGAGAAGATTCAGAAAGGAGACTCAAAAAAGGATGATGAGGAGAATTACTTGGATTT TCAGAAATTGAGAAGATTCAGAAAGGAGACTC_AAAAAGGATGATGAGGAGAATTACTTGGATTT CA C KHDRBS1 Ensembl:ENSG00000121774 Protein coding CDS GSE100210 HepG2 cell line chr1:32030325..32030326 29129909 RNA-Seq:(High) - Functional Loss DEL TCGA 33..33 33 UCEC 1 - Human_RBP_ID_19091,Human_RBP_ID_352160,Human_RBP_ID_977598,Human_RBP_ID_1154061,Human_RBP_ID_1429112,Human_RBP_ID_1745371,Human_RBP_ID_4044719,Human_RBP_ID_8308181,Human_RBP_ID_10936776,Human_RBP_ID_17452349,Human_RBP_ID_17679125,Human_RBP_ID_17748673,Human_RBP_ID_18571951,Human_RBP_ID_23387753,Human_RBP_ID_26862140 Human_Splice_Rec_42470,Human_Splice_Rec_42471,Human_Splice_Rec_42486,Human_Splice_Rec_42487,Human_Splice_Rec_42502,Human_Splice_Rec_42503,Human_Splice_Rec_42516,Human_Splice_Rec_42517 RMVar_hsa_circ_131144,RMVar_hsa_circ_300160,RMVar_hsa_circ_311133,RMVar_hsa_circ_324915,RMVar_hsa_circ_341253,RMVar_hsa_circ_309730,RMVar_hsa_circ_275865,RMVar_hsa_circ_279356,RMVar_hsa_circ_131145,RMVar_hsa_circ_131142,RMVar_hsa_circ_131143 52465 RMVar_ID_52465 Human_SNP_ID_804981611 A-to-I Human chr1 + 245101065 245101065 245101065 CACCACCACGCCCGACTAACTTTTGTATTTTTAGCAGAGATGGGGTTTCACCATGTTGGCCAGGC CACCACCACGCCCGACTAACTTTTGTATTTTTGGCAGAGATGGGGTTTCACCATGTTGGCCAGGC A G EFCAB2 Ensembl:ENSG00000203666 Protein coding intron GSE100210 HepG2 cell line chr1:245101064..245101065 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 52466 RMVar_ID_52466 Human_SNP_ID_805012083 A-to-I Human chr1 - 20755214 20755214 20755214 CTCTTTTTTATTATAGCCATACTAGTGGATATAGGGTATCTCGTTGTAGTTTTGATTGGCATTTC CTCTTTTTTATTATAGCCATACTAGTGGATATTGGGTATCTCGTTGTAGTTTTGATTGGCATTTC T A HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE112787 293 Flip-In T-REx cells,empty vector chr1:20755213..20755214 29967493 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 rectum adenocarcinoma,large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_340129,Human_RBP_ID_5747210,Human_RBP_ID_10748946 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_121886,RMVar_hsa_circ_34502,RMVar_hsa_circ_129887,RMVar_hsa_circ_129888,RMVar_hsa_circ_89876,RMVar_hsa_circ_120042,RMVar_hsa_circ_129890,RMVar_hsa_circ_129891 52467 RMVar_ID_52467 Human_SNP_ID_805020734 A-to-I Human chr1 + 166277203 166277203 166277203 TTCCATTCTGCAGTCTTGTAGGTGCAGTGGCTACTGGCTGCTGCCCATAAGCTGGATAAGCAGGC TTCCATTCTGCAGTCTTGTAGGTGCAGTGGCTGCTGGCTGCTGCCCATAAGCTGGATAAGCAGGC A G AL596087.2 Ensembl:ENSG00000229588 lincRNA intron GSE100210 HepG2 cell line chr1:166277202..166277203 29129909 RNA-Seq:(High) rs878989892 Functional Loss SNV ICGC 33..33 33 LAML 2 - 52468 RMVar_ID_52468 Human_SNP_ID_805031312 A-to-I Human chr1 + 40054444 40054444 40054444 GCAATCCACCCGTCTCGGCCTCCCAAAGTGCTAGGATTACAGGCGTGAGCCAATGTACAGTGTTT GCAATCCACCCGTCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCAATGTACAGTGTTT A G CAP1 Ensembl:ENSG00000131236 Protein coding intron GSE100210 HepG2 cell line chr1:40054443..40054444 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 6 prostate RMVar_hsa_circ_116220,RMVar_hsa_circ_131994,RMVar_hsa_circ_131993,RMVar_hsa_circ_378856 52469 RMVar_ID_52469 Human_SNP_ID_805060018 A-to-I Human chr1 - 154211278 154211278 154211278 CTATTTTTGGCCGGGCGCGGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCCGAGGAGGGT CTATTTTTGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGAGGGT T C C1orf43 Ensembl:ENSG00000143612 Protein coding intron GSE100210 HepG2 cell line chr1:154211277..154211278 29129909 RNA-Seq:(High) rs1306303006 Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 6 oesophagus Human_RBP_ID_24590670 RMVar_hsa_circ_136359,RMVar_hsa_circ_121933 52470 RMVar_ID_52470 Human_SNP_ID_805072421 A-to-I Human chr1 - 92544207 92544207 92544207 TATCTCTCCAAAAAGAAATCCTATGCTCATTTAGCTTGTCACTCCCTATTTCTCTCCAAGCCTTA TATCTCTCCAAAAAGAAATCCTATGCTCATTTGGCTTGTCACTCCCTATTTCTCTCCAAGCCTTA T C EVI5 Ensembl:ENSG00000067208 Protein coding intron GSE100210 HepG2 cell line chr1:92544206..92544207 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_116196,RMVar_hsa_circ_126531,RMVar_hsa_circ_118265,RMVar_hsa_circ_134546,RMVar_hsa_circ_134548,RMVar_hsa_circ_114279,RMVar_hsa_circ_134547,RMVar_hsa_circ_134545 52471 RMVar_ID_52471 Human_SNP_ID_805118248 A-to-I Human chr1 - 150732089 150732089 150732089 CCTGGACAACATAGTGAGACCTTGTCTCCACAAAAATAAAAAAGAAACTATCCAGGAGTGGTGGT CCTGGACAACATAGTGAGACCTTGTCTCCACACAAATAAAAAAGAAACTATCCAGGAGTGGTGGT T G CTSS Ensembl:ENSG00000163131 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells chr1:150732088..150732089 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_85933,RMVar_hsa_circ_103543,RMVar_hsa_circ_135932,RMVar_hsa_circ_135933,RMVar_hsa_circ_135934 52472 RMVar_ID_52472 Human_SNP_ID_805126378 A-to-I Human chr1 + 109626724 109626724 109626724 ACTGAGGAGAGTGATCGCATATCCTCATCTCCAGGTGCCGTTCACAGACCTGCTGGATGCAGCCA ACTGAGGAGAGTGATCGCATATCCTCATCTCCGGGTGCCGTTCACAGACCTGCTGGATGCAGCCA A G AMPD2 Ensembl:ENSG00000116337 Protein coding intron GSE105773 Glioblastoma cells,U87MG chr1:109626723..109626724 29724793 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_22634079 52473 RMVar_ID_52473 Human_SNP_ID_805142593 A-to-I Human chr1 - 166277177 166277177 166277177 AGCCAGTAGCCACTGCACCTACAAGACTGCAGAATGGAAACAAGCCCACTGAGACTAGTCAACCT AGCCAGTAGCCACTGCACCTACAAGACTGCAGGATGGAAACAAGCCCACTGAGACTAGTCAACCT T C AL596087.1 Ensembl:ENSG00000215835 Pseudogene exon GSE100210 HepG2 cell line chr1:166277176..166277177 29129909 RNA-Seq:(High) rs879211205 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_18524324 52474 RMVar_ID_52474 Human_SNP_ID_805168899 A-to-I Human chr1 + 155730192 155730192 155730192 TATACCTATATGTTCATATATGTATATATAATATTCATATATGTATATATGTATATATAATATTC TATACCTATATGTTCATATATGTATATATAATGTTCATATATGTATATATGTATATATAATATTC A G DAP3 Ensembl:ENSG00000132676 Protein coding intron GSE47997 K562 cells&HepG2 cells chr1:155730191..155730192 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_136670,RMVar_hsa_circ_124226,RMVar_hsa_circ_320226,RMVar_hsa_circ_111509,RMVar_hsa_circ_299789,RMVar_hsa_circ_59888,RMVar_hsa_circ_136682,RMVar_hsa_circ_136683,RMVar_hsa_circ_68767,RMVar_hsa_circ_49600 52475 RMVar_ID_52475 Human_SNP_ID_805170077 A-to-I Human chr1 + 45510548 45510548 45510548 GACACTAAAAAAGACTATCTCTAATCAAGGCTAGAACCAAGGGAAGGCTAAGAATTGCCCAGTAC GACACTAAAAAAGACTATCTCTAATCAAGGCTGGAACCAAGGGAAGGCTAAGAATTGCCCAGTAC A G MMACHC Ensembl:ENSG00000132763 Protein coding 3'UTR GSE38233 cultured B-cells chr1:45510547..45510548 24183664 RNA-Seq:(High) rs1044711 Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_3314521,Human_RBP_ID_5830489,Human_RBP_ID_17218818,Human_RBP_ID_17336023,Human_RBP_ID_17453328,Human_RBP_ID_26380800,Human_RBP_ID_27595210 RMVar_hsa_circ_267386,RMVar_hsa_circ_110548,RMVar_hsa_circ_132503 52476 RMVar_ID_52476 Human_SNP_ID_805184714 A-to-I Human chr1 - 150731311 150731311 150731311 CCATCTCAGTTCACTGCAACTTCTGCCTCCCGAGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGA CCATCTCAGTTCACTGCAACTTCTGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGA T C CTSS Ensembl:ENSG00000163131 Protein coding 3'UTR GSE38233 cultured B-cells chr1:150731310..150731311 24183664 RNA-Seq:(High) rs56091952 Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_98429 RMVar_hsa_circ_85933,RMVar_hsa_circ_103543,RMVar_hsa_circ_135932,RMVar_hsa_circ_135933 52477 RMVar_ID_52477 Human_SNP_ID_805206190 A-to-I Human chr1 + 32067295 32067295 32067295 GTAGTGGTACACGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGGATTGCTTGGAGCTG GTAGTGGTACACGCCTGTAATCCCAGCTACTCCGGAGGCTGAGGCAGGAGGATTGCTTGGAGCTG A C - - Other Unknown GSE100210 HepG2 cell line chr1:32067294..32067295 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 52478 RMVar_ID_52478 Human_SNP_ID_805240467 A-to-I Human chr1 - 197138579 197138579 197138579 AAGTGTGAACTCCTAGTGGGGCGTGGTGGCTCATGCCTGTGATCCCAGCACTTTGGGAGGCTGAG AAGTGTGAACTCCTAGTGGGGCGTGGTGGCTCGTGCCTGTGATCCCAGCACTTTGGGAGGCTGAG T C ASPM Ensembl:ENSG00000066279 Protein coding intron GSE100210 HepG2 cell line chr1:197138578..197138579 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_265806,RMVar_hsa_circ_357987,RMVar_hsa_circ_268720,RMVar_hsa_circ_52323,RMVar_hsa_circ_78214,RMVar_hsa_circ_138601,RMVar_hsa_circ_370738,RMVar_hsa_circ_138609,RMVar_hsa_circ_375689,RMVar_hsa_circ_68502,RMVar_hsa_circ_138610,RMVar_hsa_circ_59770 52479 RMVar_ID_52479 Human_SNP_ID_805272607 A-to-I Human chr1 + 149005200 149005200 149005200 CTCAGTTACAAGTGATTATTCGTCTAGTCTGGAAAGACCCCGGAAGCTGAGAGCTGTTGGCACCT CTCAGTTACAAGTGATTATTCGTCTAGTCTGGGAAGACCCCGGAAGCTGAGAGCTGTTGGCACCT A G PDE4DIP Ensembl:ENSG00000178104 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr1:149005199..149005200 30559470 RNA-Seq:(High) - Functional Loss SNV TCGA,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 6 large intestine Human_RBP_ID_18550060 RMVar_hsa_circ_17864,RMVar_hsa_circ_314314 52480 RMVar_ID_52480 Human_SNP_ID_805282059 A-to-I Human chr1 + 206696115 206696115 206696115 TCACCTTCATCCTACCAGTCACACGGCAGATGATTTCTTTGCCAGAAAGATCAGTGACATGGACA TCACCTTCATCCTACCAGTCACACGGCAGATGGTTTCTTTGCCAGAAAGATCAGTGACATGGACA A G MAPKAPK2 Ensembl:ENSG00000162889 Protein coding intron GSE100210 HepG2 cell line chr1:206696114..206696115 29129909 RNA-Seq:(High) rs879976912 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 haematopoietic and lymphoid tissue RMVar_hsa_circ_99465,RMVar_hsa_circ_139257 52481 RMVar_ID_52481 Human_SNP_ID_805298154 A-to-I Human chr1 - 161109365 161109365 161109365 AAATTATTTAAGTAACTAATATGCATTTTTATATGAGCACATATAAAGGGTTAACATATGGGAAT AAATTATTTAAGTAACTAATATGCATTTTTATGTGAGCACATATAAAGGGTTAACATATGGGAAT T C PFDN2 Ensembl:ENSG00000143256 Protein coding intron GSE38233 cultured B-cells chr1:161109364..161109365 24183664 RNA-Seq:(High) rs4656985 Functional Loss SNV ICGC 33..33 33 LAML 1 - Clinvar_Rec_110 GWAS_ID_4085,GWAS_ID_4086,GWAS_ID_4087,GWAS_ID_4088,GWAS_ID_4089,GWAS_ID_4090,GWAS_ID_4091,GWAS_ID_4092,GWAS_ID_4093,GWAS_ID_4094,GWAS_ID_4095,GWAS_ID_4096,GWAS_ID_4097,GWAS_ID_4098,GWAS_ID_4099,GWAS_ID_4100,GWAS_ID_4101,GWAS_ID_4102,GWAS_ID_4103,GWAS_ID_4104,GWAS_ID_4105,GWAS_ID_4106,GWAS_ID_4107,GWAS_ID_4108,GWAS_ID_4109,GWAS_ID_4110,GWAS_ID_4111,GWAS_ID_4112,GWAS_ID_4113,GWAS_ID_4114,GWAS_ID_4115,GWAS_ID_4116,GWAS_ID_4117,GWAS_ID_4118,GWAS_ID_4119,GWAS_ID_4120,GWAS_ID_4121,GWAS_ID_4122,GWAS_ID_4123,GWAS_ID_4124,GWAS_ID_4125,GWAS_ID_4126,GWAS_ID_4127,GWAS_ID_4128,GWAS_ID_4129,GWAS_ID_4130,GWAS_ID_4131,GWAS_ID_4132,GWAS_ID_4133,GWAS_ID_4134,GWAS_ID_4135,GWAS_ID_4136,GWAS_ID_4137,GWAS_ID_4138,GWAS_ID_4139,GWAS_ID_4140,GWAS_ID_4141,GWAS_ID_4142,GWAS_ID_4143,GWAS_ID_4144,GWAS_ID_4145,GWAS_ID_4146,GWAS_ID_4147,GWAS_ID_4148,GWAS_ID_4149,GWAS_ID_4150,GWAS_ID_4151,GWAS_ID_4152,GWAS_ID_4153,GWAS_ID_4154,GWAS_ID_4155,GWAS_ID_4156,GWAS_ID_4157,GWAS_ID_4158,GWAS_ID_4159,GWAS_ID_4160,GWAS_ID_4161,GWAS_ID_4162,GWAS_ID_4163,GWAS_ID_4164,GWAS_ID_4165,GWAS_ID_4166,GWAS_ID_4167,GWAS_ID_4168,GWAS_ID_4169 RMVar_hsa_circ_124680,RMVar_hsa_circ_125716,RMVar_hsa_circ_137111,RMVar_hsa_circ_137116 52482 RMVar_ID_52482 Human_SNP_ID_805315689 A-to-I Human chr1 - 91642971 91642971 91642971 TCATCTGAGTCCACCACACCCTTGACAAAATTAAGGTACTTAGGCATCATATCATGGAATTCATC TCATCTGAGTCCACCACACCCTTGACAAAATTCAGGTACTTAGGCATCATATCATGGAATTCATC T G - - Other Unknown GSE100210 HepG2 cell line chr1:91642970..91642971 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 52483 RMVar_ID_52483 Human_SNP_ID_805315695 A-to-I Human chr1 - 91642971 91642971 91642971 TCATCTGAGTCCACCACACCCTTGACAAAATTAAGGTACTTAGGCATCATATCATGGAATTCATC TCATCTGAGTCCACCACACCCTTGACAAAATTGAGGTACTTAGGCATCATATCATGGAATTCATC T C - - Other Unknown GSE100210 HepG2 cell line chr1:91642970..91642971 29129909 RNA-Seq:(High) rs879001614 Functional Loss SNV ICGC 33..33 33 STAD 1 - 52484 RMVar_ID_52484 Human_SNP_ID_805359500 A-to-I Human chr1 - 37944891 37944891 37944891 AGTTAGGCCAGGTGCAGTAGCTCATGCTTGTAATTCCAACACTTTGGGAGGCTGAGGCAGGAAGA AGTTAGGCCAGGTGCAGTAGCTCATGCTTGTACTTCCAACACTTTGGGAGGCTGAGGCAGGAAGA T G INPP5B Ensembl:ENSG00000204084 Protein coding intron GSE47997 K562 cells&HepG2 cells chr1:37944890..37944891 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 6 breast RMVar_hsa_circ_343429,RMVar_hsa_circ_81814,RMVar_hsa_circ_131764,RMVar_hsa_circ_265587 52485 RMVar_ID_52485 Human_SNP_ID_805390383 A-to-I Human chr1 - 21778696 21778696 21778696 GGTGCCCAAGCTGGTCTTGAACTCCTTGCTTCAAGTGATCCTCCTGCCTTGGCCCCCTGAAATGC GGTGCCCAAGCTGGTCTTGAACTCCTTGCTTCGAGTGATCCTCCTGCCTTGGCCCCCTGAAATGC T C USP48 Ensembl:ENSG00000090686 Protein coding intron GSE100210 HepG2 cell line chr1:21778695..21778696 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 52486 RMVar_ID_52486 Human_SNP_ID_805406011 A-to-I Human chr1 + 100018709 100018709 100018709 GCTTTGTTGCCCAGGCTGATCTTGAACTCCTTACCTCGAGCAATCTTCCCACCTCTGCCTCTCAG GCTTTGTTGCCCAGGCTGATCTTGAACTCCTTCCCTCGAGCAATCTTCCCACCTCTGCCTCTCAG A C AC118553.2,SLC35A3 Ensembl:ENSG00000283761,Ensembl:ENSG00000117620 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line chr1:100018708..100018709 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_10487652 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 52487 RMVar_ID_52487 Human_SNP_ID_805430799 A-to-I Human chr1 + 113111233 113111233 113111233 AATTTTTGTATTTTTAGTAGAGACAAAGTTTCACCATTTTGGCCAGGTTGGTCTCAGACTCCTGA AATTTTTGTATTTTTAGTAGAGACAAAGTTTCGCCATTTTGGCCAGGTTGGTCTCAGACTCCTGA A G LRIG2 Ensembl:ENSG00000198799 Protein coding intron GSE100210 HepG2 cell line chr1:113111232..113111233 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 2 pancreas Human_RBP_ID_10529404 RMVar_hsa_circ_1467,RMVar_hsa_circ_369936,RMVar_hsa_circ_285223,RMVar_hsa_circ_290837,RMVar_hsa_circ_4790,RMVar_hsa_circ_46169,RMVar_hsa_circ_292752,RMVar_hsa_circ_135408,RMVar_hsa_circ_135409,RMVar_hsa_circ_303440,RMVar_hsa_circ_135407,RMVar_hsa_circ_284758,RMVar_hsa_circ_135421,RMVar_hsa_circ_135422,RMVar_hsa_circ_135420,RMVar_hsa_circ_292963,RMVar_hsa_circ_135425,RMVar_hsa_circ_18646,RMVar_hsa_circ_135429,RMVar_hsa_circ_32200,RMVar_hsa_circ_97621,RMVar_hsa_circ_76395,RMVar_hsa_circ_331345,RMVar_hsa_circ_359675,RMVar_hsa_circ_135430 52488 RMVar_ID_52488 Human_SNP_ID_805440616 A-to-I Human chr1 + 168251250 168251250 168251250 AGGCACAAGAATTGCTTGAACCCAGGAGGTGGAAGTTCAGTGAGCCGAGATCGCACCCCTGCACT AGGCACAAGAATTGCTTGAACCCAGGAGGTGGCAGTTCAGTGAGCCGAGATCGCACCCCTGCACT A C SFT2D2 Ensembl:ENSG00000213064 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line chr1:168251250..168251251 29129909,31158229,31158229,31158229 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_5709704,Human_RBP_ID_10645110 52489 RMVar_ID_52489 Human_SNP_ID_805501266 A-to-I Human chr1 + 40180358 40180358 40180358 TTGACTCATTGTAACCTCTGCCTCCTGGAATCAAGTGATTCTCCTGCCTCAGCCTCCTGAGTGGC TTGACTCATTGTAACCTCTGCCTCCTGGAATCGAGTGATTCTCCTGCCTCAGCCTCCTGAGTGGC A G RLF Ensembl:ENSG00000117000 Protein coding intron GSE38233 cultured B-cells chr1:40180357..40180358 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_120866,RMVar_hsa_circ_132013,RMVar_hsa_circ_132015 52490 RMVar_ID_52490 Human_SNP_ID_805509379 A-to-I Human chr1 + 91642661 91642661 91642661 TCAAAGACTAAAAAAGTTGAAAACACTGTCTGAGACTGGGAACTTATGAATGATATCAAACCAGT TCAAAGACTAAAAAAGTTGAAAACACTGTCTGGGACTGGGAACTTATGAATGATATCAAACCAGT A G HSP90B3P Ensembl:ENSG00000203914 Pseudogene exon GSE100210 HepG2 cell line chr1:91642660..91642661 29129909 RNA-Seq:(High) rs879023619 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_17456676 52491 RMVar_ID_52491 Human_SNP_ID_805521028 A-to-I Human chr1 - 31046300 31046300 31046300 CTCACCGCAACCTCCACCTCCCGGGTTCAAGCAATTCTCCTGCCTTAGCCTCCCGAGTAGCTGTG CTCACCGCAACCTCCACCTCCCGGGTTCAAGCGATTCTCCTGCCTTAGCCTCCCGAGTAGCTGTG T C PUM1 Ensembl:ENSG00000134644 Protein coding intron GSE38233 cultured B-cells chr1:31046299..31046300 24183664 RNA-Seq:(High) rs1255879951 Functional Loss SNV ICGC 33..33 33 PRAD 1 - 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 52492 RMVar_ID_52492 Human_SNP_ID_805544341 A-to-I Human chr1 - 150602052 150602052 150602052 TTGCCCAGGCTGATCTTGAATTCCTGGACTCAAGCGATCTGCCTGCCTTGGCCTCCCAAAATGCT TTGCCCAGGCTGATCTTGAATTCCTGGACTCACGCGATCTGCCTGCCTTGGCCTCCCAAAATGCT T G ENSA Ensembl:ENSG00000143420 Protein coding intron GSE100210 HepG2 cell line chr1:150602051..150602052 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 52493 RMVar_ID_52493 Human_SNP_ID_805553275 A-to-I Human chr1 - 30947996 30947996 30947996 AAAAAGTTGGCTGGGCATGGTGGTGCACTCCTATAGTCTCAGCTGCTTGGGGTGCTAAGGCAGGA AAAAAGTTGGCTGGGCATGGTGGTGCACTCCTGTAGTCTCAGCTGCTTGGGGTGCTAAGGCAGGA T C PUM1 Ensembl:ENSG00000134644 Protein coding intron GSE38233 cultured B-cells chr1:30947995..30947996 24183664 RNA-Seq:(High) rs751725792 Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_22861822,Human_RBP_ID_24682321 RMVar_hsa_circ_121030,RMVar_hsa_circ_130983,RMVar_hsa_circ_124647,RMVar_hsa_circ_371999,RMVar_hsa_circ_348445,RMVar_hsa_circ_278509,RMVar_hsa_circ_36810,RMVar_hsa_circ_83915,RMVar_hsa_circ_130984,RMVar_hsa_circ_130985,RMVar_hsa_circ_130986,RMVar_hsa_circ_315757,RMVar_hsa_circ_327662,RMVar_hsa_circ_372758,RMVar_hsa_circ_320131,RMVar_hsa_circ_312856,RMVar_hsa_circ_298189,RMVar_hsa_circ_306228,RMVar_hsa_circ_130987,RMVar_hsa_circ_130989,RMVar_hsa_circ_130990,RMVar_hsa_circ_130988,RMVar_hsa_circ_109101,RMVar_hsa_circ_116545,RMVar_hsa_circ_86432,RMVar_hsa_circ_130993,RMVar_hsa_circ_78901,RMVar_hsa_circ_130995,RMVar_hsa_circ_130996,RMVar_hsa_circ_130997,RMVar_hsa_circ_130994,RMVar_hsa_circ_86246,RMVar_hsa_circ_338078,RMVar_hsa_circ_372401,RMVar_hsa_circ_346873,RMVar_hsa_circ_274987,RMVar_hsa_circ_67706,RMVar_hsa_circ_130999,RMVar_hsa_circ_25419,RMVar_hsa_circ_31601,RMVar_hsa_circ_131000,RMVar_hsa_circ_131001,RMVar_hsa_circ_130998 52494 RMVar_ID_52494 Human_SNP_ID_805572136 A-to-I Human chr1 + 204527148 204527146 204527148 GAAACCCTGTCTCTAAAAAAAAAAAAAAAAATACAAAAATTGGGCGGGCATGGTGGTCTGCTCGT GAAACCCTGTCTCTAAAAAAAAAAAAAAAAA__CAAAAATTGGGCGGGCATGGTGGTCTGCTCGT ATA A MDM4 Ensembl:ENSG00000198625 Protein coding intron GSE100210 HepG2 cell line chr1:204527147..204527148 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 32..33 33 LMS 1 - RMVar_hsa_circ_118234,RMVar_hsa_circ_139147,RMVar_hsa_circ_123815,RMVar_hsa_circ_367720,RMVar_hsa_circ_284316,RMVar_hsa_circ_22678,RMVar_hsa_circ_89387,RMVar_hsa_circ_139149,RMVar_hsa_circ_92157,RMVar_hsa_circ_139150,RMVar_hsa_circ_139148,RMVar_hsa_circ_348206,RMVar_hsa_circ_79149,RMVar_hsa_circ_139152,RMVar_hsa_circ_139153 52495 RMVar_ID_52495 Human_SNP_ID_805606972 A-to-I Human chr1 - 75234041 75234041 75234041 AGTTGGATATTTTTGATACTTCTGAGGTTCATAGCTGGATGCCTCTTCTGGGTCTTCATGATTGG AGTTGGATATTTTTGATACTTCTGAGGTTCATCGCTGGATGCCTCTTCTGGGTCTTCATGATTGG T G SLC44A5 Ensembl:ENSG00000137968 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector chr1:75234040..75234041 29967493 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,right_upper_lobe adenocarcinoma,LUAD 4 lung Human_RBP_ID_362101,Human_RBP_ID_3321567 Human_Splice_Rec_87122,Human_Splice_Rec_87123,Human_Splice_Rec_87168,Human_Splice_Rec_87169 RMVar_hsa_circ_2301,RMVar_hsa_circ_49547,RMVar_hsa_circ_40319,RMVar_hsa_circ_17404,RMVar_hsa_circ_10970,RMVar_hsa_circ_42194,RMVar_hsa_circ_48348,RMVar_hsa_circ_37737,RMVar_hsa_circ_49231,RMVar_hsa_circ_318784,RMVar_hsa_circ_6435,RMVar_hsa_circ_345900,RMVar_hsa_circ_319363,RMVar_hsa_circ_13101,RMVar_hsa_circ_266878,RMVar_hsa_circ_285906,RMVar_hsa_circ_133961,RMVar_hsa_circ_321272,RMVar_hsa_circ_305531,RMVar_hsa_circ_318879,RMVar_hsa_circ_53214,RMVar_hsa_circ_19914,RMVar_hsa_circ_133963,RMVar_hsa_circ_133964,RMVar_hsa_circ_133965,RMVar_hsa_circ_133962,RMVar_hsa_circ_133966 52496 RMVar_ID_52496 Human_SNP_ID_805619753 A-to-I Human chr1 + 220316886 220316886 220316886 TCCACAGACAAAGCCAGGACTCGTTTGTACCCATTGATGATAGAATGGGGTACTGATGCAACAGT TCCACAGACAAAGCCAGGACTCGTTTGTACCCTTTGATGATAGAATGGGGTACTGATGCAACAGT A T - - Other Unknown GSE100210 HepG2 cell line chr1:220316885..220316886 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 52497 RMVar_ID_52497 Human_SNP_ID_805641244 A-to-I Human chr1 - 155204014 155204013 155204014 CCAACACTGTGAAACCTCCTCTCTACTAAAAAATACAAAAAATTAGCTGGGCATGGTGGTGGGCA CCAACACTGTGAAACCTCCTCTCTACTAAAAA_TACAAAAAATTAGCTGGGCATGGTGGTGGGCA AT A THBS3 Ensembl:ENSG00000169231 Protein coding intron GSE47997 K562 cells&HepG2 cells chr1:155204013..155204014 23474544 RNA-Seq:(High) - Functional Loss DEL ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_17320,RMVar_hsa_circ_49762,RMVar_hsa_circ_107213,RMVar_hsa_circ_136519 52498 RMVar_ID_52498 Human_SNP_ID_805661919 A-to-I Human chr1 - 20649616 20649616 20649616 GAATTACAGGCGTGTGCCACGACACTCAGCTAATTTTTGTATTTTTAGTACAGACGGGGTTTTAC GAATTACAGGCGTGTGCCACGACACTCAGCTATTTTTTGTATTTTTAGTACAGACGGGGTTTTAC T A PINK1-AS Ensembl:ENSG00000117242 lincRNA exon GSE38233 cultured B-cells chr1:20649615..20649616 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 52499 RMVar_ID_52499 Human_SNP_ID_805713936 A-to-I Human chr1 - 220058802 220058802 220058802 TCATTTGGCCGGGCGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGTGG TCATTTGGCCGGGCGCGGTGGCTCATGCCTGTGATCCCAGCACTTTGGGAGGCCGAGGCAGGTGG T C BPNT1 Ensembl:ENSG00000162813 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr1:220058801..220058802 24183664,29129909 RNA-Seq:(High) rs3201546 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 haematopoietic and lymphoid tissue 52500 RMVar_ID_52500 Human_SNP_ID_805714893 A-to-I Human chr1 + 32842626 32842626 32842626 CATTTTATTTTATTTTTTTGAGATGGAGTCTCACTCTGTTGCCTAGGCTGTCGTGCGGTGGTGCG CATTTTATTTTATTTTTTTGAGATGGAGTCTCGCTCTGTTGCCTAGGCTGTCGTGCGGTGGTGCG A G S100PBP Ensembl:ENSG00000116497 Protein coding intron GSE38233 cultured B-cells chr1:32842625..32842626 24183664 RNA-Seq:(High) rs1025516049 Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_10948353 RMVar_hsa_circ_90137,RMVar_hsa_circ_131305,RMVar_hsa_circ_273527,RMVar_hsa_circ_131307,RMVar_hsa_circ_17462 52501 RMVar_ID_52501 Human_SNP_ID_805717111 A-to-I Human chr1 - 153824254 153824254 153824254 ATGAGGTGTTGCTGTGTTGCCCAGGCTGACGTACATTGGCTGTTCACAAGCACTGTCATAGTGCA ATGAGGTGTTGCTGTGTTGCCCAGGCTGACGTGCATTGGCTGTTCACAAGCACTGTCATAGTGCA T C GATAD2B Ensembl:ENSG00000143614 Protein coding intron GSE38233 cultured B-cells chr1:153824253..153824254 24183664 RNA-Seq:(High) rs75860520 Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_32482,RMVar_hsa_circ_356213,RMVar_hsa_circ_344971,RMVar_hsa_circ_46063,RMVar_hsa_circ_360643 52502 RMVar_ID_52502 Human_SNP_ID_805728973 A-to-I Human chr1 + 203306471 203306471 203306471 CTGTCAGTTTTGGGAAGCGATAGCCATCTCGGAACGCACCCACACAGACCCTGCCTTCTGAGGAA CTGTCAGTTTTGGGAAGCGATAGCCATCTCGGGACGCACCCACACAGACCCTGCCTTCTGAGGAA A G BTG2 Ensembl:ENSG00000159388 Protein coding intron GSE100210 HepG2 cell line chr1:203306471..203306472 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue Burkitt_lymphoma 2 haematopoietic and lymphoid tissue RMVar_hsa_circ_103046,RMVar_hsa_circ_139032 52503 RMVar_ID_52503 Human_SNP_ID_805731353 A-to-I Human chr1 + 151203271 151203271 151203271 GCACTTGAGGCTGGGTACAATGGCTCACACCTATATTCTCAGCACTTTGGGAGGCCAAGGCAGGC GCACTTGAGGCTGGGTACAATGGCTCACACCTGTATTCTCAGCACTTTGGGAGGCCAAGGCAGGC A G PIP5K1A Ensembl:ENSG00000143398 Protein coding intron GSE100210 HepG2 cell line chr1:151203270..151203271 29129909 RNA-Seq:(High) rs971665496 Functional Loss SNV ICGC 33..33 33 MALY 1 - 52504 RMVar_ID_52504 Human_SNP_ID_805732290 A-to-I Human chr1 - 20755323 20755323 20755323 AGTGAAGTAGTCTGCCTGCCTCAGCTTCCCAAAGTGTTGGAATTACAGGTGTGATCCACCACACC AGTGAAGTAGTCTGCCTGCCTCAGCTTCCCAAGGTGTTGGAATTACAGGTGTGATCCACCACACC T C HP1BP3 Ensembl:ENSG00000127483 Protein coding intron GSE38233 cultured B-cells chr1:20755322..20755323 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue Human_RBP_ID_340133,Human_RBP_ID_17557009 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_121886,RMVar_hsa_circ_34502,RMVar_hsa_circ_129887,RMVar_hsa_circ_129888,RMVar_hsa_circ_89876,RMVar_hsa_circ_120042,RMVar_hsa_circ_129890,RMVar_hsa_circ_129891 52505 RMVar_ID_52505 Human_SNP_ID_805803706 A-to-I Human chr1 - 52512189 52512189 52512189 GAGATAGAATCAGGCTGTAGTGATACAGCTTTATCCAAGGTCAGTTGAGATGTCCTCTGATGCCT GAGATAGAATCAGGCTGTAGTGATACAGCTTTGTCCAAGGTCAGTTGAGATGTCCTCTGATGCCT T C TUT4 Ensembl:ENSG00000134744 Protein coding intron GSE100210 HepG2 cell line chr1:52512188..52512189 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 3 liver Human_RBP_ID_3316908,Human_RBP_ID_17556670,Human_RBP_ID_24710681 RMVar_hsa_circ_56837,RMVar_hsa_circ_88452,RMVar_hsa_circ_132969,RMVar_hsa_circ_121402,RMVar_hsa_circ_132992,RMVar_hsa_circ_67601,RMVar_hsa_circ_61539,RMVar_hsa_circ_378205,RMVar_hsa_circ_32729,RMVar_hsa_circ_4981,RMVar_hsa_circ_113320,RMVar_hsa_circ_63614,RMVar_hsa_circ_324946,RMVar_hsa_circ_368345,RMVar_hsa_circ_133020,RMVar_hsa_circ_133021,RMVar_hsa_circ_329383,RMVar_hsa_circ_17200,RMVar_hsa_circ_133026,RMVar_hsa_circ_65331,RMVar_hsa_circ_270080,RMVar_hsa_circ_358627,RMVar_hsa_circ_133030,RMVar_hsa_circ_133032,RMVar_hsa_circ_133033,RMVar_hsa_circ_133034,RMVar_hsa_circ_133031 52506 RMVar_ID_52506 Human_SNP_ID_805828968 A-to-I Human chr1 + 26704705 26704705 26704705 TAACATAGGGAGACCCCATCTTTACAAGACACAAAAATTGCTGGATGTGGTGGTACGTGCCTGTA TAACATAGGGAGACCCCATCTTTACAAGACACCAAAATTGCTGGATGTGGTGGTACGTGCCTGTA A C ARID1A Ensembl:ENSG00000117713 Protein coding intron GSE100210 HepG2 cell line chr1:26704705..26704706 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 4 oesophagus Human_RBP_ID_17557046 RMVar_hsa_circ_268846 52507 RMVar_ID_52507 Human_SNP_ID_805847791 A-to-I Human chr1 - 151453090 151453090 151453090 TGGTGAAACCTGTCTCTACTAAAAATACAAAAATTAGCTGGGCGTTGTGGCGCATGCATGTAATC TGGTGAAACCTGTCTCTACTAAAAATACAAAATTTAGCTGGGCGTTGTGGCGCATGCATGTAATC T A POGZ Ensembl:ENSG00000143442 Protein coding intron GSE107867 ASD brains,cerebellum chr1:151453089..151453090 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - 52508 RMVar_ID_52508 Human_SNP_ID_805886762 A-to-I Human chr1 + 32683762 32683762 32683762 TCAAGCGATTCTCCTGCCTTGGCCTCCTGAGTAGCTGGGATTATAAGTGCCTGCCACTATGCCCG TCAAGCGATTCTCCTGCCTTGGCCTCCTGAGTTGCTGGGATTATAAGTGCCTGCCACTATGCCCG A T RBBP4 Ensembl:ENSG00000162521 Protein coding 3'UTR GSE47997;GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 K562 cells&HepG2 cells;cultured B-cells;Bronchiolar epithelium,BEP2D cell line chr1:32683761..32683762 23474544,24183664,31158229 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 52509 RMVar_ID_52509 Human_SNP_ID_805889918 A-to-I Human chr1 - 9101599 9101599 9101599 AACCTCCAAAAAGTTATACATCAGGTATCTCTAGTCAGCTTCCTCCGCTGCCCACCTCTTGCCAC AACCTCCAAAAAGTTATACATCAGGTATCTCTTGTCAGCTTCCTCCGCTGCCCACCTCTTGCCAC T A GPR157 Ensembl:ENSG00000180758 Protein coding 3'UTR GSE38233 cultured B-cells chr1:9101598..9101599 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_365129,Human_RBP_ID_4069413 52510 RMVar_ID_52510 Human_SNP_ID_805912482 A-to-I Human chr1 + 220467994 220467994 220467994 CTGGACTTCGGAGCACGTCTTTGACCACCCATAGGAAACTGTTACAACAGCTGCAATGCAGAAAT CTGGACTTCGGAGCACGTCTTTGACCACCCATGGGAAACTGTTACAACAGCTGCAATGCAGAAAT A G PRELID3BP1 Ensembl:ENSG00000226226 Pseudogene exon GSE100210 HepG2 cell line chr1:220467993..220467994 29129909 RNA-Seq:(High) rs1188483438 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_26375665 Human_miRNA_ID_1823548,Human_miRNA_ID_1835879,Human_miRNA_ID_1838730 52511 RMVar_ID_52511 Human_SNP_ID_805929383 A-to-I Human chr1 - 217454829 217454829 217454829 AGGAGTTTGAGACCAGCCTGGCCAATAAGGTGAAACCCCCGTCTCTAGTAAAAATATGAAAATTA AGGAGTTTGAGACCAGCCTGGCCAATAAGGTGGAACCCCCGTCTCTAGTAAAAATATGAAAATTA T C GPATCH2 Ensembl:ENSG00000092978 Protein coding intron GSE47997 K562 cells&HepG2 cells chr1:217454828..217454829 23474544 RNA-Seq:(High) rs1323546738 Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_289885,RMVar_hsa_circ_366693 52512 RMVar_ID_52512 Human_SNP_ID_805937385 A-to-I Human chr1 - 52993367 52993367 52993367 ACACAGGAAGAAGGACGGCAGTTAGCACGGCAACTTAAGGTAACATACATGGAGGCATCAGCAAA ACACAGGAAGAAGGACGGCAGTTAGCACGGCAGCTTAAGGTAACATACATGGAGGCATCAGCAAA T C RRAS2P1 Ensembl:ENSG00000236360 Pseudogene exon GSE107867 ASD brains,cerebellum chr1:52993366..52993367 30559470 RNA-Seq:(High) rs878879572 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 haematopoietic and lymphoid tissue 52513 RMVar_ID_52513 Human_SNP_ID_805965477 A-to-I Human chr1 + 14713663 14713663 14713663 GCCCCAAGTGTCAGTATTGCCAAGGCTAGCCGAGTACAGTGGCTTATGCCTGTAATCCTAGTATT GCCCCAAGTGTCAGTATTGCCAAGGCTAGCCGGGTACAGTGGCTTATGCCTGTAATCCTAGTATT A G KAZN Ensembl:ENSG00000189337 Protein coding intron GSE47997 K562 cells&HepG2 cells chr1:14713662..14713663 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 52514 RMVar_ID_52514 Human_SNP_ID_805967013 A-to-I Human chr1 + 171762379 171762379 171762379 GGCGTGGTCACAGCTACTCTAGAGGTGGTGGGAACCAGGACTATGGGAGTGGCAGGTATGACAGT GGCGTGGTCACAGCTACTCTAGAGGTGGTGGGGACCAGGACTATGGGAGTGGCAGGTATGACAGT A G Z98751.2 Ensembl:ENSG00000236741 Pseudogene exon GSE100210 HepG2 cell line chr1:171762378..171762379 29129909 RNA-Seq:(High) rs1463739982 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_5890114,Human_RBP_ID_8241454 52515 RMVar_ID_52515 Human_SNP_ID_805978863 A-to-I Human chr1 + 155315562 155315562 155315562 AATATTAGCCGGGCATGGTGGCAGGCGCCTGTAGTCCCAGCTATTTGGGAGGCTGAGGTAGGAGA AATATTAGCCGGGCATGGTGGCAGGCGCCTGTCGTCCCAGCTATTTGGGAGGCTGAGGTAGGAGA A C FDPS Ensembl:ENSG00000160752 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr1:155315561..155315562 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 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 52516 RMVar_ID_52516 Human_SNP_ID_806027402 A-to-I Human chr1 - 39855008 39855008 39855008 CCTTACCTCTACAAAAAATACAAAAATTAGCCAGATGTGGTGGCATGTGCTTGTAGTCCCAGCTA CCTTACCTCTACAAAAAATACAAAAATTAGCCGGATGTGGTGGCATGTGCTTGTAGTCCCAGCTA T C TRIT1 Ensembl:ENSG00000043514 Protein coding intron GSE38233 cultured B-cells chr1:39855007..39855008 24183664 RNA-Seq:(High) rs1442299640 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 6 liver RMVar_hsa_circ_120389,RMVar_hsa_circ_377449,RMVar_hsa_circ_131971,RMVar_hsa_circ_131974,RMVar_hsa_circ_131975,RMVar_hsa_circ_326611,RMVar_hsa_circ_131976,RMVar_hsa_circ_104330,RMVar_hsa_circ_25192,RMVar_hsa_circ_36919,RMVar_hsa_circ_131977,RMVar_hsa_circ_87369,RMVar_hsa_circ_131978,RMVar_hsa_circ_131985,RMVar_hsa_circ_131980,RMVar_hsa_circ_131979,RMVar_hsa_circ_289012,RMVar_hsa_circ_131981,RMVar_hsa_circ_311725,RMVar_hsa_circ_321660,RMVar_hsa_circ_281554,RMVar_hsa_circ_131983,RMVar_hsa_circ_131984,RMVar_hsa_circ_131982 52517 RMVar_ID_52517 Human_SNP_ID_806064039 A-to-I Human chr1 + 26711246 26711246 26711246 TTTTCCTGCCTCAGCCTCTCGTAGCTGGGATTACAGGTCCACGCCACCACGCCCGGCTAATTTTA TTTTCCTGCCTCAGCCTCTCGTAGCTGGGATTGCAGGTCCACGCCACCACGCCCGGCTAATTTTA A G ARID1A Ensembl:ENSG00000117713 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr1:26711245..26711246 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LMS 1 - RMVar_hsa_circ_268846 52518 RMVar_ID_52518 Human_SNP_ID_806080596 A-to-I Human chr1 + 87046417 87046417 87046417 ACCCTGAAGCTGCCTGGGAACCAACAGAAGCCAAAGCCAGAGCTAGAACATTCTAATAAAGAAGG ACCCTGAAGCTGCCTGGGAACCAACAGAAGCCGAAGCCAGAGCTAGAACATTCTAATAAAGAAGG A G AC093155.1,HS2ST1,AC093155.3 Ensembl:ENSG00000225568,Ensembl:ENSG00000153936,Ensembl:ENSG00000267561 Pseudogene,Protein coding,Protein coding exon,intron,intron GSE100210 HepG2 cell line chr1:87046416..87046417 29129909 RNA-Seq:(High) rs879200517 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 8 haematopoietic and lymphoid tissue Human_RBP_ID_8242589,Human_RBP_ID_17586671,Human_RBP_ID_26383775 52519 RMVar_ID_52519 Human_SNP_ID_806096970 A-to-I Human chr1 - 1098136 1098136 1098136 AAAACCCTAGAGGTGGAGCTGGCAGTGAGCCAAGATCGCACCACTGCACTCCAGCCTGGGTGACA AAAACCCTAGAGGTGGAGCTGGCAGTGAGCCACGATCGCACCACTGCACTCCAGCCTGGGTGACA T G C1orf159 Ensembl:ENSG00000131591 Protein coding intron GSE100210 HepG2 cell line chr1:1098135..1098136 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 2 - 52520 RMVar_ID_52520 Human_SNP_ID_806222214 A-to-I Human chr1 + 117082237 117082235 117082237 TAAGCATAATAATAATTCTTATTTTTTGAGACAGGGTCTCGCTCTGTTGCTCAGGCTGGAGTGCA TAAGCATAATAATAATTCTTATTTTTTGAGA__GGGTCTCGCTCTGTTGCTCAGGCTGGAGTGCA ACA A TTF2 Ensembl:ENSG00000116830 Protein coding intron GSE100210 HepG2 cell line chr1:117082236..117082237 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 32..33 33 LMS 1 - Human_miRNA_ID_1949954,Human_miRNA_ID_1951238,Human_miRNA_ID_2443323 RMVar_hsa_circ_116031,RMVar_hsa_circ_119088,RMVar_hsa_circ_96197,RMVar_hsa_circ_135648,RMVar_hsa_circ_135649,RMVar_hsa_circ_135651,RMVar_hsa_circ_92212,RMVar_hsa_circ_135654,RMVar_hsa_circ_101578,RMVar_hsa_circ_110065,RMVar_hsa_circ_135652,RMVar_hsa_circ_80085,RMVar_hsa_circ_135655,RMVar_hsa_circ_126216,RMVar_hsa_circ_135653,RMVar_hsa_circ_120763,RMVar_hsa_circ_135656,RMVar_hsa_circ_110780,RMVar_hsa_circ_93760,RMVar_hsa_circ_135658,RMVar_hsa_circ_98395,RMVar_hsa_circ_135659,RMVar_hsa_circ_135660,RMVar_hsa_circ_78374,RMVar_hsa_circ_88077,RMVar_hsa_circ_135661,RMVar_hsa_circ_135662,RMVar_hsa_circ_135663 52521 RMVar_ID_52521 Human_SNP_ID_806231525 A-to-I Human chr1 - 1598505 1598505 1598505 GCCATCACCACTGGGTCCCAGGGCAGAAGCTTAGATACCGGCCTTGAGCAGCCCGACCTTCCACC GCCATCACCACTGGGTCCCAGGGCAGAAGCTTGGATACCGGCCTTGAGCAGCCCGACCTTCCACC T C FNDC10 Ensembl:ENSG00000228594 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector chr1:1598504..1598505 29967493 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_326705,Human_RBP_ID_19192905,Human_RBP_ID_22127868,Human_RBP_ID_26799709 52522 RMVar_ID_52522 Human_SNP_ID_806239253 A-to-I Human chr1 - 52160415 52160415 52160415 ATAGAAAGGCACTGCCTTTGGAGGATGGAAGAATGTAGAAAGTGTCCCAAAGTTGGTGTCTGAAT ATAGAAAGGCACTGCCTTTGGAGGATGGAAGAGTGTAGAAAGTGTCCCAAAGTTGGTGTCTGAAT T C AL139156.2 Ensembl:ENSG00000228407 Pseudogene exon GSE100210 HepG2 cell line chr1:52160414..52160415 29129909 RNA-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_5890997 52523 RMVar_ID_52523 Human_SNP_ID_806243794 A-to-I Human chr1 + 150309014 150309014 150309014 GGAGAAGTAAGGAATTTTTTTTTCTTTTTTTTAAGAGGAAGTCTCGCTCTTGTCCCCCAGACTGG GGAGAAGTAAGGAATTTTTTTTTCTTTTTTTTGAGAGGAAGTCTCGCTCTTGTCCCCCAGACTGG A G - - Other Unknown GSE100210 HepG2 cell line chr1:150309013..150309014 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_2092836,Human_RBP_ID_5686403,Human_RBP_ID_10568229,Human_RBP_ID_23143822,Human_RBP_ID_26367858 52524 RMVar_ID_52524 Human_SNP_ID_806256171 A-to-I Human chr1 - 220058801 220058801 220058801 CATTTGGCCGGGCGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGTGGA CATTTGGCCGGGCGCGGTGGCTCATGCCTGTAGTCCCAGCACTTTGGGAGGCCGAGGCAGGTGGA T C BPNT1 Ensembl:ENSG00000162813 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr1:220058800..220058801 24183664,29129909 RNA-Seq:(High) rs1137752 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 haematopoietic and lymphoid tissue 52525 RMVar_ID_52525 Human_SNP_ID_806259336 A-to-I Human chr1 + 202582778 202582778 202582778 GTGGTGGCAGGCGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATGGCGTGAACCCG GTGGTGGCAGGCGCCTGTAGTCCCAGCTACTCTGGAGGCTGAGGCAGGAGAATGGCGTGAACCCG A T PPP1R12B Ensembl:ENSG00000077157 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank chr1:202582777..202582778 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_97738,RMVar_hsa_circ_138943,RMVar_hsa_circ_268759 52526 RMVar_ID_52526 Human_SNP_ID_806261531 A-to-I Human chr1 - 246842627 246842627 246842627 TGATTGAGACAGTCTCGCTCTGTCCCCACCCTACTATCCTCCTTTTATTATTTTATTTTATTTTT TGATTGAGACAGTCTCGCTCTGTCCCCACCCTCCTATCCTCCTTTTATTATTTTATTTTATTTTT T G AHCTF1 Ensembl:ENSG00000153207 Protein coding intron GSE100210 HepG2 cell line chr1:246842626..246842627 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast lobular_carcinoma 3 breast RMVar_hsa_circ_265981 52527 RMVar_ID_52527 Human_SNP_ID_806277782 A-to-I Human chr1 + 150099333 150099332 150099333 CCTGGCCAACATAGTGAAACCTTGTCTCTACTAAAAAAAAAAATACAAAAATTAGCCGGGTGTGG CCTGGCCAACATAGTGAAACCTTGTCTCTACT_AAAAAAAAAATACAAAAATTAGCCGGGTGTGG TA T VPS45 Ensembl:ENSG00000136631 Protein coding intron GSE47997 K562 cells&HepG2 cells chr1:150099332..150099333 23474544 RNA-Seq:(High) rs1181008396 Functional Loss DEL ICGC 33..33 33 MALY 1 - 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 52528 RMVar_ID_52528 Human_SNP_ID_806320820 A-to-I Human chr1 - 146081471 146081471 146081471 TCTGAATGTATTGCAGGAATTAAAAAGGACCAAGAAGAGGAAGAAGACCAAGGCCCACCATGCCC TCTGAATGTATTGCAGGAATTAAAAAGGACCAGGAAGAGGAAGAAGACCAAGGCCCACCATGCCC T C NBPF10 Ensembl:ENSG00000271425 Protein coding CDS GSE107867 ASD brains,cerebellum chr1:146081470..146081471 30559470 RNA-Seq:(High) rs1159226650 Functional Loss SNV TCGA 33..33 33 BRCA 1 - Human_RBP_ID_17340295 Human_Splice_Rec_119328,Human_Splice_Rec_119329,Human_Splice_Rec_119504,Human_Splice_Rec_119505 52529 RMVar_ID_52529 Human_SNP_ID_850844960 A-to-I Human chr4 - 88131869 88131869 88131869 GCTGCAAGGAAAGATCCAAGTGGATTATCTGGAGATGTTCTGATAAATGGAGCACCGCGACCTGC GCTGCAAGGAAAGATCCAAGTGGATTATCTGGGGATGTTCTGATAAATGGAGCACCGCGACCTGC T C ABCG2 Ensembl:ENSG00000118777 Protein coding CDS GSE100210 HepG2 cell line chr4:88131868..88131869 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_Splice_Rec_581896,Human_Splice_Rec_581897,Human_Splice_Rec_581926,Human_Splice_Rec_581927,Human_Splice_Rec_581956,Human_Splice_Rec_581957,Human_Splice_Rec_581986,Human_Splice_Rec_581992 RMVar_hsa_circ_352746,RMVar_hsa_circ_73149,RMVar_hsa_circ_364801,RMVar_hsa_circ_67959,RMVar_hsa_circ_51780,RMVar_hsa_circ_313149 52530 RMVar_ID_52530 Human_SNP_ID_851136539 A-to-I Human chr4 + 172236480 172236480 172236480 TACTTGGGAGGCTGAGGCAGGAGAATGGCATGAACCCGGGAGGCAGGGCTTGCAGTGAGCCAAGA TACTTGGGAGGCTGAGGCAGGAGAATGGCATGCACCCGGGAGGCAGGGCTTGCAGTGAGCCAAGA A C GALNTL6 Ensembl:ENSG00000174473 Protein coding intron GSE47997 K562 cells&HepG2 cells chr4:172236480..172236481 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_297687,RMVar_hsa_circ_349403,RMVar_hsa_circ_46517,RMVar_hsa_circ_229559,RMVar_hsa_circ_10649 52531 RMVar_ID_52531 Human_SNP_ID_851187872 A-to-I Human chr4 - 117084822 117084822 117084822 TCCTGAACTCTACTTCCAGAAAACCAAAAAACAAGACATCCCTCGTCAACTTGTCTACATTGGTC TCCTGAACTCTACTTCCAGAAAACCAAAAAACGAGACATCCCTCGTCAACTTGTCTACATTGGTC T C TRAM1L1 Ensembl:ENSG00000174599 Protein coding CDS GSE38233 cultured B-cells chr4:117084822..117084823 24183664 RNA-Seq:(High) rs755408129 Functional Loss SNV ICGC 33..33 33 ESCA 1 - 52532 RMVar_ID_52532 Human_SNP_ID_851279293 A-to-I Human chr4 - 139290970 139290970 139290970 CCATCAGTACTAAAAATACACAAAAAATAGCTAGGCATGGTGGTGCGCGCCCGTAGTCCCAGCTA CCATCAGTACTAAAAATACACAAAAAATAGCTTGGCATGGTGGTGCGCGCCCGTAGTCCCAGCTA T A NDUFC1 Ensembl:ENSG00000109390 Protein coding intron GSE38233 cultured B-cells chr4:139290969..139290970 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 7 prostate RMVar_hsa_circ_228692 52533 RMVar_ID_52533 Human_SNP_ID_851431443 A-to-I Human chr4 + 102751993 102751993 102751993 ATGCTGGAAGTGCAGAGTCTATAGCTGTTGATAGCTCAGGAACTAAATTTTGTAGTGGCTCCTGG ATGCTGGAAGTGCAGAGTCTATAGCTGTTGATGGCTCAGGAACTAAATTTTGTAGTGGCTCCTGG A G AC018797.2 Ensembl:ENSG00000251288 Pseudogene exon GSE38233 cultured B-cells chr4:102751992..102751993 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 haematopoietic and lymphoid tissue 52534 RMVar_ID_52534 Human_SNP_ID_851465383 A-to-I Human chr4 - 57110120 57110120 57110120 AGGGCGAGCCGTGCGGGGGTGGCGGCGCCGGCAGGGGGTACTGCGCGCCGGGCATGGAGTGCGTG AGGGCGAGCCGTGCGGGGGTGGCGGCGCCGGCGGGGGGTACTGCGCGCCGGGCATGGAGTGCGTG T C IGFBP7 Ensembl:ENSG00000163453 Protein coding CDS GSE100210;GSE107867 HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr4:57110119..57110120 29129909,30559470 RNA-Seq:(High) rs11555284 Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_27508817 52535 RMVar_ID_52535 Human_SNP_ID_851493141 A-to-I Human chr4 + 39464590 39464590 39464590 ACAGTCATAGCTCACTGCAGCCTCGAACTCCTAGGCTCAAGTAATCCTCCTATCTCAGCCTCCCT ACAGTCATAGCTCACTGCAGCCTCGAACTCCTTGGCTCAAGTAATCCTCCTATCTCAGCCTCCCT A T LIAS Ensembl:ENSG00000121897 Protein coding intron GSE100210 HepG2 cell line chr4:39464589..39464590 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_46082 52536 RMVar_ID_52536 Human_SNP_ID_851545933 A-to-I Human chr4 - 82822817 82822817 82822817 AGGCATGTGCCACCACGCCCGGCTAATTTTGTATTTTTAGAAGAGACAGGGTTTCTCCATGTTGG AGGCATGTGCCACCACGCCCGGCTAATTTTGTTTTTTTAGAAGAGACAGGGTTTCTCCATGTTGG T A SEC31A Ensembl:ENSG00000138674 Protein coding intron GSE100210 HepG2 cell line chr4:82822816..82822817 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 14 prostate RMVar_hsa_circ_226986,RMVar_hsa_circ_90287,RMVar_hsa_circ_98687,RMVar_hsa_circ_125182,RMVar_hsa_circ_91568,RMVar_hsa_circ_226988,RMVar_hsa_circ_226989,RMVar_hsa_circ_226987,RMVar_hsa_circ_226990,RMVar_hsa_circ_66157,RMVar_hsa_circ_334451,RMVar_hsa_circ_366391,RMVar_hsa_circ_357911,RMVar_hsa_circ_294456,RMVar_hsa_circ_226991 52537 RMVar_ID_52537 Human_SNP_ID_851590002 A-to-I Human chr4 + 127837045 127837045 127837045 TCACTGCAGCCTCCACCACCTGAGTTCAAGCGATTTTTCTGCCTCAACCTCTCCTGAGTAGCTGG TCACTGCAGCCTCCACCACCTGAGTTCAAGCGCTTTTTCTGCCTCAACCTCTCCTGAGTAGCTGG A C HSPA4L Ensembl:ENSG00000164070 Protein coding 3'UTR GSE100210 HepG2 cell line chr4:127837044..127837045 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 52538 RMVar_ID_52538 Human_SNP_ID_851648218 A-to-I Human chr4 + 2970623 2970623 2970623 GAGGTTGCAGTGAGCCGAGATCGTGCCACTGCACTCCAACCTGGCGACACGGTGAGACTCCATCT GAGGTTGCAGTGAGCCGAGATCGTGCCACTGCCCTCCAACCTGGCGACACGGTGAGACTCCATCT A C GRK4 Ensembl:ENSG00000125388 Protein coding intron GSE100210 HepG2 cell line chr4:2970622..2970623 29129909 RNA-Seq:(High) rs899576784 Functional Loss SNV ICGC 33..33 33 ESCA 1 - 52539 RMVar_ID_52539 Human_SNP_ID_851653684 A-to-I Human chr4 + 108661071 108661071 108661071 AAAACCAGTCTCTACTAAAAAATAAAAAAATTAGCTGGGCGTGGTAGTGCACGCCTGTAATCCCA AAAACCAGTCTCTACTAAAAAATAAAAAAATTTGCTGGGCGTGGTAGTGCACGCCTGTAATCCCA A T OSTC Ensembl:ENSG00000198856 Protein coding intron GSE38233 cultured B-cells chr4:108661070..108661071 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_104578,RMVar_hsa_circ_107374,RMVar_hsa_circ_227921,RMVar_hsa_circ_227923 52540 RMVar_ID_52540 Human_SNP_ID_851732538 A-to-I Human chr4 + 39774183 39774183 39774183 AAAAAATGCTGGGTGTGGTGGTGTGTGCCTGTAGTCCCAGCTACTCGTGAGGCTGAGGCAGGAGA AAAAAATGCTGGGTGTGGTGGTGTGTGCCTGTTGTCCCAGCTACTCGTGAGGCTGAGGCAGGAGA A T UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE38233 cultured B-cells chr4:39774182..39774183 24183664 RNA-Seq:(High) rs1307793579 Functional Loss SNV ICGC 33..33 33 PRAD 1 - RMVar_hsa_circ_225460,RMVar_hsa_circ_225465,RMVar_hsa_circ_225464,RMVar_hsa_circ_225459,RMVar_hsa_circ_225463,RMVar_hsa_circ_225468,RMVar_hsa_circ_298369,RMVar_hsa_circ_225467,RMVar_hsa_circ_225472,RMVar_hsa_circ_271227,RMVar_hsa_circ_225471,RMVar_hsa_circ_225476,RMVar_hsa_circ_225474,RMVar_hsa_circ_287533,RMVar_hsa_circ_313227,RMVar_hsa_circ_225473,RMVar_hsa_circ_225477,RMVar_hsa_circ_279938,RMVar_hsa_circ_280268,RMVar_hsa_circ_225478 52541 RMVar_ID_52541 Human_SNP_ID_851781683 A-to-I Human chr4 + 128032506 128032506 128032506 CAGGAGTTCGAGCCCAGCCTGGCCAATATGGTAAAACCCCGTCTCTACTAAAAATACAAAAATTA CAGGAGTTCGAGCCCAGCCTGGCCAATATGGTGAAACCCCGTCTCTACTAAAAATACAAAAATTA A G ABHD18 Ensembl:ENSG00000164074 Protein coding intron GSE38233 cultured B-cells chr4:128032505..128032506 24183664 RNA-Seq:(High) rs949035334 Functional Loss SNV ICGC 33..33 33 CMDI 1 - 52542 RMVar_ID_52542 Human_SNP_ID_851784234 A-to-I Human chr4 - 121370161 121370161 121370161 CAGCATCCCTTGGAAGCCAGTGATTTCAGAGCACAAGTATCAGCACCTCACCAAGGTGGAGGAAG CAGCATCCCTTGGAAGCCAGTGATTTCAGAGCGCAAGTATCAGCACCTCACCAAGGTGGAGGAAG T C AC093816.1,QRFPR Ensembl:ENSG00000213480,Ensembl:ENSG00000186867 Pseudogene,Protein coding exon,intron GSE100210 HepG2 cell line chr4:121370160..121370161 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue 52543 RMVar_ID_52543 Human_SNP_ID_852012406 A-to-I Human chr4 - 55529368 55529368 55529368 ATTGCTTGAAGCTAGGAGTTTGAGACTAGCCTAGGCAACATAATGAGACCCCATCTCTACAAGAA ATTGCTTGAAGCTAGGAGTTTGAGACTAGCCTGGGCAACATAATGAGACCCCATCTCTACAAGAA T C CLOCK Ensembl:ENSG00000134852 Protein coding intron GSE100210 HepG2 cell line chr4:55529367..55529368 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_114662,RMVar_hsa_circ_226136,RMVar_hsa_circ_226147 52544 RMVar_ID_52544 Human_SNP_ID_852035160 A-to-I Human chr4 - 79902115 79902115 79902115 AAATGTCAGTGGGTGATCCAAAATAAATTGTTAAAGTTATTAAAATGTACATTTAAGTAGGTTTC AAATGTCAGTGGGTGATCCAAAATAAATTGTTCAAGTTATTAAAATGTACATTTAAGTAGGTTTC T G ANTXR2 Ensembl:ENSG00000163297 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells chr4:79902114..79902115 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 2 pancreas 52545 RMVar_ID_52545 Human_SNP_ID_852115023 A-to-I Human chr4 + 128021507 128021507 128021507 CCAACCCCATCACTACTAAAAATACAAAAATTAGCCACGTGTGGTGGTAGGTGCCTGTAATCCCA CCAACCCCATCACTACTAAAAATACAAAAATTTGCCACGTGTGGTGGTAGGTGCCTGTAATCCCA A T ABHD18 Ensembl:ENSG00000164074 Protein coding intron GSE100210 HepG2 cell line chr4:128021506..128021507 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_279023,RMVar_hsa_circ_288390,RMVar_hsa_circ_228537,RMVar_hsa_circ_228538,RMVar_hsa_circ_228549,RMVar_hsa_circ_68990,RMVar_hsa_circ_305903,RMVar_hsa_circ_228553,RMVar_hsa_circ_228548,RMVar_hsa_circ_366571,RMVar_hsa_circ_280129,RMVar_hsa_circ_297020,RMVar_hsa_circ_283242,RMVar_hsa_circ_57132,RMVar_hsa_circ_228554,RMVar_hsa_circ_228555 52546 RMVar_ID_52546 Human_SNP_ID_852234368 A-to-I Human chr4 + 2476634 2476634 2476634 CAGCCTGTCTCGAACTCCTGACCTTGTGATCCACCCACCTCGGCCTCCCAAAGTGCTGGGATTAC CAGCCTGTCTCGAACTCCTGACCTTGTGATCCCCCCACCTCGGCCTCCCAAAGTGCTGGGATTAC A C RNF4 Ensembl:ENSG00000063978 Protein coding intron GSE100210 HepG2 cell line chr4:2476633..2476634 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_15129879 RMVar_hsa_circ_28096,RMVar_hsa_circ_124524,RMVar_hsa_circ_224355 52547 RMVar_ID_52547 Human_SNP_ID_852284463 A-to-I Human chr4 + 112375254 112375254 112375254 TCAGCCGGAGTGTAGAGGTGCAGTCACAGCTCACTCCAGCCTCAATCTCCTGGGCTCAAGCAATC TCAGCCGGAGTGTAGAGGTGCAGTCACAGCTCGCTCCAGCCTCAATCTCCTGGGCTCAAGCAATC A G ALPK1 Ensembl:ENSG00000073331 Protein coding intron GSE47997 K562 cells&HepG2 cells chr4:112375253..112375254 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_228007,RMVar_hsa_circ_108897 52548 RMVar_ID_52548 Human_SNP_ID_852340700 A-to-I Human chr4 + 153495168 153495168 153495168 GAAACCCCATCTCTACTAAAAATACAAAAATTAGCCGGGCGTGGTGGTATGCACCAGTAGTCCCA GAAACCCCATCTCTACTAAAAATACAAAAATTGGCCGGGCGTGGTGGTATGCACCAGTAGTCCCA A G TMEM131L Ensembl:ENSG00000121210 Protein coding intron GSE38233 cultured B-cells chr4:153495167..153495168 24183664 RNA-Seq:(High) rs886369678 Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_111567,RMVar_hsa_circ_229225,RMVar_hsa_circ_89179,RMVar_hsa_circ_229224 52549 RMVar_ID_52549 Human_SNP_ID_852358907 A-to-I Human chr4 + 8454424 8454424 8454424 AAAGGGCACTGTAACAACCATTCCAAGCTCTTAGAGGCGTAGGCAAATATGTGCAGGCCATCAGT AAAGGGCACTGTAACAACCATTCCAAGCTCTTCGAGGCGTAGGCAAATATGTGCAGGCCATCAGT A C TRMT44 Ensembl:ENSG00000155275 Protein coding intron GSE38233 cultured B-cells chr4:8454423..8454424 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_52245,RMVar_hsa_circ_7235,RMVar_hsa_circ_64709,RMVar_hsa_circ_293683,RMVar_hsa_circ_224801 52550 RMVar_ID_52550 Human_SNP_ID_852367878 A-to-I Human chr4 + 183483824 183483824 183483824 CACACCAGGAGGGCGAGGAGACATGAAATATGACATATATGCTGTAGAGAATGAGCATATGAATC CACACCAGGAGGGCGAGGAGACATGAAATATGGCATATATGCTGTAGAGAATGAGCATATGAATC A G VTI1BP2 Ensembl:ENSG00000213434 Pseudogene exon GSE100210 HepG2 cell line chr4:183483823..183483824 29129909 RNA-Seq:(High) rs1358003806 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_17409731 52551 RMVar_ID_52551 Human_SNP_ID_852395943 A-to-I Human chr4 + 87892974 87892974 87892974 TGAGTTGATACCAGAGTATCTCAATTTTATCCATGGTGTGGTTGACTCTGAGGATCTGCCCCTGA TGAGTTGATACCAGAGTATCTCAATTTTATCCGTGGTGTGGTTGACTCTGAGGATCTGCCCCTGA A G HSP90AB3P Ensembl:ENSG00000183199 Pseudogene exon GSE100210 HepG2 cell line chr4:87892973..87892974 29129909 RNA-Seq:(High) rs765948573 Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_1107083,Human_RBP_ID_8265953,Human_RBP_ID_9261661,Human_RBP_ID_17706440,Human_RBP_ID_18032672,Human_RBP_ID_18409615,Human_RBP_ID_18517861,Human_RBP_ID_21082880,Human_RBP_ID_22511101 52552 RMVar_ID_52552 Human_SNP_ID_852544507 A-to-I Human chr4 - 189957414 189957414 189957414 CATTGCATCTAATAAAGCAGCTATTTGAGGCCAACAAAGCCATTTTCCCCTAAGTGAAACAAATA CATTGCATCTAATAAAGCAGCTATTTGAGGCCGACAAAGCCATTTTCCCCTAAGTGAAACAAATA T C lnc-FRG2-11 RNACentral:URS00008BB8A8 lincRNA intron GSE107867 ASD brains,temporal_cortex chr4:189957413..189957414 30559470 RNA-Seq:(High) rs575384276 Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma,large_intestine adenocarcinoma 11 prostate,large intestine 52553 RMVar_ID_52553 Human_SNP_ID_852611828 A-to-I Human chr4 - 189943223 189943223 189943223 GTTTCTTCATCTTCTTCTCTTTTTCTTTTCTTATCTTTGCTCTTTTTCTTCTTACTACAGGACAT GTTTCTTCATCTTCTTCTCTTTTTCTTTTCTTCTCTTTGCTCTTTTTCTTCTTACTACAGGACAT T G - - Other Unknown GSE38233 cultured B-cells chr4:189943222..189943223 24183664 RNA-Seq:(High) rs373444578 Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 1 kidney 52554 RMVar_ID_52554 Human_SNP_ID_852774345 A-to-I Human chr4 + 17627076 17627076 17627076 ACCTCTGCCTCCCGGGTTCAAGTAATTTTCCTACGTCAGCCTCCCGAGTAGCTGTCAGGTGCACA ACCTCTGCCTCCCGGGTTCAAGTAATTTTCCTTCGTCAGCCTCCCGAGTAGCTGTCAGGTGCACA A T MED28 Ensembl:ENSG00000118579 Protein coding 3'UTR GSE38233 cultured B-cells chr4:17627075..17627076 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_15098763,Human_RBP_ID_24045767 52555 RMVar_ID_52555 Human_SNP_ID_852876860 A-to-I Human chr4 - 21522474 21522474 21522474 CACATTTAGTCATAGCTACTCAGGAGGCCGGAAGATCGCTTGAGCCCAGGAGTTAGAGGCTGCAG CACATTTAGTCATAGCTACTCAGGAGGCCGGATGATCGCTTGAGCCCAGGAGTTAGAGGCTGCAG T A KCNIP4,AC096576.6 Ensembl:ENSG00000185774,Ensembl:ENSG00000286318 Protein coding,lincRNA intron,exon GSE107867 ASD brains,frontal_cortex chr4:21522473..21522474 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_16582 52556 RMVar_ID_52556 Human_SNP_ID_852919119 A-to-I Human chr4 + 96902887 96902887 96902887 GCTTCCCACAGGCATTTTAAAAATAAAGTTCCAGAGAAACAAAAACTGTTCCAGGAGGATGATGG GCTTCCCACAGGCATTTTAAAAATAAAGTTCCGGAGAAACAAAAACTGTTCCAGGAGGATGATGG A G COX7A2P2 Ensembl:ENSG00000236764 Pseudogene exon GSE100210 HepG2 cell line chr4:96902886..96902887 29129909 RNA-Seq:(High) rs879206966 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_8596607 52557 RMVar_ID_52557 Human_SNP_ID_852985771 A-to-I Human chr4 - 165075223 165075223 165075223 AAAAAAAAAAGAAAGAAAAGAAAAAAAATTGTATTTCTAGTAGAGACGGGGATTCACCATGTTGG AAAAAAAAAAGAAAGAAAAGAAAAAAAATTGTCTTTCTAGTAGAGACGGGGATTCACCATGTTGG T G TMEM192 Ensembl:ENSG00000170088 Protein coding 3'UTR GSE100210 HepG2 cell line chr4:165075222..165075223 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 52558 RMVar_ID_52558 Human_SNP_ID_853005456 A-to-I Human chr4 + 143875834 143875834 143875834 CTGCTATTAAAAAAATACAAAAATTAGTCAGGAATGGTGGCCCGCACCTGTAGTCCCAACTACTG CTGCTATTAAAAAAATACAAAAATTAGTCAGGCATGGTGGCCCGCACCTGTAGTCCCAACTACTG A C AC107223.1 Ensembl:ENSG00000251600 lincRNA intron GSE100210 HepG2 cell line chr4:143875834..143875835 29129909 RNA-Seq:(High) rs80063093 Functional Loss SNV ICGC,COSMIC 33..33 33 prostate adenocarcinoma,STAD,pancreas ductal_carcinoma 9 pancreas,prostate RMVar_hsa_circ_228821,RMVar_hsa_circ_336685 52559 RMVar_ID_52559 Human_SNP_ID_853032767 A-to-I Human chr4 + 68376350 68376350 68376350 TCGCCATGGATCCCAACTGCTCCTGTGCCGCCAGTGACTCCTGCACCTGCGCCGGCTCCTGCAAG TCGCCATGGATCCCAACTGCTCCTGTGCCGCCGGTGACTCCTGCACCTGCGCCGGCTCCTGCAAG A G MT2P1 Ensembl:ENSG00000162840 Pseudogene exon GSE100210 HepG2 cell line chr4:68376349..68376350 29129909 RNA-Seq:(High) rs768785878 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_8265938 52560 RMVar_ID_52560 Human_SNP_ID_853043898 A-to-I Human chr4 + 109840907 109840907 109840907 TTTCTTTTGGGGGAATTTCTAATTGTCTCTGTAGTTATTATTACTATTATGACCACCATCATCAT TTTCTTTTGGGGGAATTTCTAATTGTCTCTGTGGTTATTATTACTATTATGACCACCATCATCAT A G RRH Ensembl:ENSG00000180245 Protein coding intron GSE100210 HepG2 cell line chr4:109840906..109840907 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - Human_RBP_ID_9148890 52561 RMVar_ID_52561 Human_SNP_ID_853124634 A-to-I Human chr4 - 82863396 82863396 82863396 GGTCTTTGTTTTAAGAATATGTCTTTTTTTTTAAAGGTAAACTTTGAGGATGATTCTCGTGGAAA GGTCTTTGTTTTAAGAATATGTCTTTTTTTTTTAAGGTAAACTTTGAGGATGATTCTCGTGGAAA T A SEC31A Ensembl:ENSG00000138674 Protein coding intron GSE100210 HepG2 cell line chr4:82863395..82863396 29129909 RNA-Seq:(High) rs927953902 Functional Loss SNV ICGC,COSMIC 33..33 33 caecum adenocarcinoma,LICA,liver neoplasm,large_intestine adenocarcinoma 45 caecum,liver,large intestine Human_RBP_ID_71440,Human_RBP_ID_15211268 Human_Splice_Rec_574203,Human_Splice_Rec_574269,Human_Splice_Rec_574317,Human_Splice_Rec_574361,Human_Splice_Rec_574413,Human_Splice_Rec_574463,Human_Splice_Rec_574513,Human_Splice_Rec_574563,Human_Splice_Rec_574615,Human_Splice_Rec_574661,Human_Splice_Rec_574717,Human_Splice_Rec_574761,Human_Splice_Rec_574813,Human_Splice_Rec_574881,Human_Splice_Rec_574903,Human_Splice_Rec_574919,Human_Splice_Rec_574931 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_20979,RMVar_hsa_circ_66854,RMVar_hsa_circ_119957,RMVar_hsa_circ_226996,RMVar_hsa_circ_66529,RMVar_hsa_circ_99033,RMVar_hsa_circ_331988,RMVar_hsa_circ_41586,RMVar_hsa_circ_226998,RMVar_hsa_circ_227008,RMVar_hsa_circ_120871,RMVar_hsa_circ_309134,RMVar_hsa_circ_350923,RMVar_hsa_circ_226999,RMVar_hsa_circ_367722,RMVar_hsa_circ_22264,RMVar_hsa_circ_227002,RMVar_hsa_circ_227003,RMVar_hsa_circ_227005,RMVar_hsa_circ_119465,RMVar_hsa_circ_327749,RMVar_hsa_circ_287866,RMVar_hsa_circ_227006,RMVar_hsa_circ_227004,RMVar_hsa_circ_118538,RMVar_hsa_circ_370517,RMVar_hsa_circ_374948,RMVar_hsa_circ_297624,RMVar_hsa_circ_227010,RMVar_hsa_circ_227011,RMVar_hsa_circ_227009,RMVar_hsa_circ_69666,RMVar_hsa_circ_353898,RMVar_hsa_circ_265470,RMVar_hsa_circ_74473,RMVar_hsa_circ_3876,RMVar_hsa_circ_319636,RMVar_hsa_circ_369488,RMVar_hsa_circ_310758,RMVar_hsa_circ_227016,RMVar_hsa_circ_57386,RMVar_hsa_circ_33499,RMVar_hsa_circ_321663,RMVar_hsa_circ_227015,RMVar_hsa_circ_323349,RMVar_hsa_circ_14613,RMVar_hsa_circ_18797,RMVar_hsa_circ_227020,RMVar_hsa_circ_227019,RMVar_hsa_circ_356828,RMVar_hsa_circ_64636,RMVar_hsa_circ_350914,RMVar_hsa_circ_227021 52562 RMVar_ID_52562 Human_SNP_ID_853125119 A-to-I Human chr4 - 39955945 39955945 39955945 ATGTCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCGCCATGTTGGCCAGGCTGGTCTC ATGTCTGGCTAATTTTTGTATTTTTAGTAGAGGTGGGGTTTCGCCATGTTGGCCAGGCTGGTCTC T C PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE47997 K562 cells&HepG2 cells chr4:39955944..39955945 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - RMVar_hsa_circ_118437,RMVar_hsa_circ_225482,RMVar_hsa_circ_115099,RMVar_hsa_circ_101014,RMVar_hsa_circ_225524,RMVar_hsa_circ_225525,RMVar_hsa_circ_52264,RMVar_hsa_circ_62955,RMVar_hsa_circ_5363 52563 RMVar_ID_52563 Human_SNP_ID_853142415 A-to-I Human chr4 - 21784121 21784121 21784121 CTTCGACCCCACCCCCCACCGCCTTGTGAAGAAGGTGCCTGCTTCTCCTTTGCCTTCTGCCATGA CTTCGACCCCACCCCCCACCGCCTTGTGAAGATGGTGCCTGCTTCTCCTTTGCCTTCTGCCATGA T A KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,temporal_cortex chr4:21784120..21784121 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 52564 RMVar_ID_52564 Human_SNP_ID_853227594 A-to-I Human chr4 - 39832082 39832082 39832082 ATGGAGTCTTGCTCTGTCACCCAGGCTGGAGTACAATGGTGAGATCTCGGCTCACTGCACCCTCT ATGGAGTCTTGCTCTGTCACCCAGGCTGGAGTCCAATGGTGAGATCTCGGCTCACTGCACCCTCT T G PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE38233 cultured B-cells chr4:39832081..39832082 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_25834510 RMVar_hsa_circ_96208,RMVar_hsa_circ_118437,RMVar_hsa_circ_127708,RMVar_hsa_circ_268799,RMVar_hsa_circ_120167,RMVar_hsa_circ_117569,RMVar_hsa_circ_225482,RMVar_hsa_circ_225484,RMVar_hsa_circ_225486,RMVar_hsa_circ_85409,RMVar_hsa_circ_225487,RMVar_hsa_circ_225485,RMVar_hsa_circ_225483 52565 RMVar_ID_52565 Human_SNP_ID_853234406 A-to-I Human chr4 + 41680064 41680064 41680064 GCTGAAAGAAGAGTGGGAAAAGGCCCAAAAGGAGGTGGAAGAGGAAGAACGCAGATACTATGAGG GCTGAAAGAAGAGTGGGAAAAGGCCCAAAAGGTGGTGGAAGAGGAAGAACGCAGATACTATGAGG A T LIMCH1 Ensembl:ENSG00000064042 Protein coding CDS GSE100210 HepG2 cell line chr4:41680063..41680064 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 14 lung Human_RBP_ID_72432,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 52566 RMVar_ID_52566 Human_SNP_ID_853280653 A-to-I Human chr4 + 147974766 147974766 147974766 GACATACCCAAGACTGGGAAATTTACAAATGAAAGAGGTTTAATGGGCTCATGGTTCCACAGGGC GACATACCCAAGACTGGGAAATTTACAAATGATAGAGGTTTAATGGGCTCATGGTTCCACAGGGC A T ARHGAP10 Ensembl:ENSG00000071205 Protein coding intron GSE100210 HepG2 cell line chr4:147974766..147974767 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 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_107190,RMVar_hsa_circ_354715,RMVar_hsa_circ_47608,RMVar_hsa_circ_228941,RMVar_hsa_circ_228942,RMVar_hsa_circ_111243,RMVar_hsa_circ_76535,RMVar_hsa_circ_24369,RMVar_hsa_circ_300736,RMVar_hsa_circ_228944,RMVar_hsa_circ_228943,RMVar_hsa_circ_314784,RMVar_hsa_circ_228949,RMVar_hsa_circ_305386,RMVar_hsa_circ_31096,RMVar_hsa_circ_228951,RMVar_hsa_circ_312575,RMVar_hsa_circ_348149 52567 RMVar_ID_52567 Human_SNP_ID_853361118 A-to-I Human chr4 + 1898216 1898216 1898216 TCAAGCGATCCTCCTGCCTCAGCCTCCTGAGTAGCAGGGACTACAGGTGCACATCACCACGACTG TCAAGCGATCCTCCTGCCTCAGCCTCCTGAGTTGCAGGGACTACAGGTGCACATCACCACGACTG A T NSD2 Ensembl:ENSG00000109685 Protein coding intron GSE38233 cultured B-cells chr4:1898215..1898216 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_224288,RMVar_hsa_circ_115170,RMVar_hsa_circ_224291,RMVar_hsa_circ_224290,RMVar_hsa_circ_79323 52568 RMVar_ID_52568 Human_SNP_ID_853416425 A-to-I Human chr4 + 2499076 2499076 2499076 AAAATTAGACGGGCGTGGTGGCGGGCGCCTGTAATCCCAGCTACTTGGGAGGTTGATGCAGGAGA AAAATTAGACGGGCGTGGTGGCGGGCGCCTGTGATCCCAGCTACTTGGGAGGTTGATGCAGGAGA A G RNF4 Ensembl:ENSG00000063978 Protein coding intron GSE38233 cultured B-cells chr4:2499075..2499076;chr4:2499076..2499077 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 7 pancreas RMVar_hsa_circ_28096,RMVar_hsa_circ_124524,RMVar_hsa_circ_224355,RMVar_hsa_circ_284304,RMVar_hsa_circ_224357,RMVar_hsa_circ_224358,RMVar_hsa_circ_309590 52569 RMVar_ID_52569 Human_SNP_ID_853437092 A-to-I Human chr4 + 185217533 185217533 185217533 GAAAGTCTTCCAAGTTGAATGTTCTACTTGGCACCTTCTTAATTCTGGTCATTCCCAGGGGATTT GAAAGTCTTCCAAGTTGAATGTTCTACTTGGCGCCTTCTTAATTCTGGTCATTCCCAGGGGATTT A G SNX25 Ensembl:ENSG00000109762 Protein coding intron GSE38233 cultured B-cells chr4:185217532..185217533 24183664 RNA-Seq:(High) rs3108291 Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 4 pancreas Human_RBP_ID_24048447 GWAS_ID_4805,GWAS_ID_4806,GWAS_ID_4807,GWAS_ID_4808,GWAS_ID_4809,GWAS_ID_4810,GWAS_ID_4811,GWAS_ID_4812,GWAS_ID_4813,GWAS_ID_4814,GWAS_ID_4815,GWAS_ID_4816,GWAS_ID_4817,GWAS_ID_4818,GWAS_ID_4819,GWAS_ID_4820,GWAS_ID_4821,GWAS_ID_4822,GWAS_ID_4823,GWAS_ID_4824,GWAS_ID_4825,GWAS_ID_4826,GWAS_ID_4827,GWAS_ID_4828,GWAS_ID_4829,GWAS_ID_4830,GWAS_ID_4831,GWAS_ID_4832,GWAS_ID_4833,GWAS_ID_4834,GWAS_ID_4835,GWAS_ID_4836,GWAS_ID_4837,GWAS_ID_4838,GWAS_ID_4839,GWAS_ID_4840,GWAS_ID_4841,GWAS_ID_4842,GWAS_ID_4843,GWAS_ID_4844,GWAS_ID_4845,GWAS_ID_4846,GWAS_ID_4847,GWAS_ID_4848,GWAS_ID_4849,GWAS_ID_4850,GWAS_ID_4851,GWAS_ID_4852,GWAS_ID_4853,GWAS_ID_4854,GWAS_ID_4855,GWAS_ID_4856,GWAS_ID_4857,GWAS_ID_4858,GWAS_ID_4859,GWAS_ID_4860,GWAS_ID_4861,GWAS_ID_4862,GWAS_ID_4863,GWAS_ID_4864,GWAS_ID_4865,GWAS_ID_4866,GWAS_ID_4867,GWAS_ID_4868,GWAS_ID_4869,GWAS_ID_4870,GWAS_ID_4871,GWAS_ID_4872 RMVar_hsa_circ_93131,RMVar_hsa_circ_229811 52570 RMVar_ID_52570 Human_SNP_ID_853508953 A-to-I Human chr4 - 40995701 40995701 40995701 GCAAGACCCTGTCTCTGTAAAATTAAAAAATTAGCCAGACATAGTGGCACATGCTGGCGTCAGCT GCAAGACCCTGTCTCTGTAAAATTAAAAAATTTGCCAGACATAGTGGCACATGCTGGCGTCAGCT T A APBB2 Ensembl:ENSG00000163697 Protein coding intron GSE100210 HepG2 cell line chr4:40995700..40995701 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_225622,RMVar_hsa_circ_75653,RMVar_hsa_circ_92794,RMVar_hsa_circ_225621,RMVar_hsa_circ_74397,RMVar_hsa_circ_63287,RMVar_hsa_circ_106814,RMVar_hsa_circ_367502,RMVar_hsa_circ_68066,RMVar_hsa_circ_24060,RMVar_hsa_circ_116296,RMVar_hsa_circ_225633,RMVar_hsa_circ_225634,RMVar_hsa_circ_225635 52571 RMVar_ID_52571 Human_SNP_ID_853580828 A-to-I Human chr4 - 116599273 116599273 116599273 TCGGCCTCACCCTGCCGGTCGTTCTCCACGTCATAGCCCAGGCTGATGAGGCAGGCCTTGAACCC TCGGCCTCACCCTGCCGGTCGTTCTCCACGTCGTAGCCCAGGCTGATGAGGCAGGCCTTGAACCC T C - - Other Unknown GSE100210 HepG2 cell line chr4:116599272..116599273 29129909 RNA-Seq:(High) rs879212717 Functional Loss SNV ICGC 33..33 33 LAML 1 - 52572 RMVar_ID_52572 Human_SNP_ID_853603974 A-to-I Human chr4 - 117575560 117575560 117575560 TTGTGGCAGAATCTGACGTTATGCTCAAAGAAAGATATGAAGAATTTCTTTGATAAGCTCCAACA TTGTGGCAGAATCTGACGTTATGCTCAAAGAAGGATATGAAGAATTTCTTTGATAAGCTCCAACA T C NT5C3AP1 Ensembl:ENSG00000213492 Pseudogene exon GSE38233 cultured B-cells chr4:117575559..117575560 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_5607591 52573 RMVar_ID_52573 Human_SNP_ID_853630186 A-to-I Human chr4 + 103573990 103573990 103573990 CACAGTGGTGAAGGTGGCCACGGCAGCAGCAGAAGATTTGGTGGAGGTGGCTATGGAGGCTTTTG CACAGTGGTGAAGGTGGCCACGGCAGCAGCAGCAGATTTGGTGGAGGTGGCTATGGAGGCTTTTG A C AC105460.2,DDX3P3 Ensembl:ENSG00000251577,Ensembl:ENSG00000251571 lincRNA,Pseudogene intron,exon GSE100210 HepG2 cell line chr4:103573990..103573991 29129909 RNA-Seq:(High) rs2757675 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_4796261,Human_RBP_ID_7342726,Human_RBP_ID_8265912,Human_RBP_ID_8876297,Human_RBP_ID_23028062 GWAS_ID_1930,GWAS_ID_1931 52574 RMVar_ID_52574 Human_SNP_ID_853636086 A-to-I Human chr4 - 86925382 86925382 86925382 CAAAACCCCATCTCAAAATACAAAAATTAGCTAGATGTGGTGGTGCATGCCCATAATCCTAGCTA CAAAACCCCATCTCAAAATACAAAAATTAGCTGGATGTGGTGGTGCATGCCCATAATCCTAGCTA T C AC093827.4,AC093827.5 Ensembl:ENSG00000284968,Ensembl:ENSG00000285458 lincRNA,Protein coding exon,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr4:86925381..86925382 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 52575 RMVar_ID_52575 Human_SNP_ID_853683555 A-to-I Human chr4 - 78180916 78180916 78180916 CAAACCGTGGCAGCAGGACCGACAAGTCAAGTACTTCTGCTCCTGATGTGGATGACCCAGAGGCA CAAACCGTGGCAGCAGGACCGACAAGTCAAGTGCTTCTGCTCCTGATGTGGATGACCCAGAGGCA T C SERBP1P5 Ensembl:ENSG00000249565 Pseudogene exon GSE100210 HepG2 cell line chr4:78180915..78180916 29129909 RNA-Seq:(High) rs879226484 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 haematopoietic and lymphoid tissue Human_RBP_ID_5607764,Human_RBP_ID_9165583 52576 RMVar_ID_52576 Human_SNP_ID_853689038 A-to-I Human chr4 + 113320455 113320455 113320455 GTGGACGGATCATGAGGTCAGGGGTTTGAGACAAGCCTGAACAACATGGTGAAACCTCATCTCTA GTGGACGGATCATGAGGTCAGGGGTTTGAGACTAGCCTGAACAACATGGTGAAACCTCATCTCTA A T ANK2 Ensembl:ENSG00000145362 Protein coding intron GSE107867 ASD brains,frontal_cortex chr4:113320455..113320456 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - RMVar_hsa_circ_14214,RMVar_hsa_circ_34903,RMVar_hsa_circ_30631,RMVar_hsa_circ_19487,RMVar_hsa_circ_53252,RMVar_hsa_circ_42811,RMVar_hsa_circ_6935,RMVar_hsa_circ_321013,RMVar_hsa_circ_8304,RMVar_hsa_circ_13795,RMVar_hsa_circ_228108,RMVar_hsa_circ_265274,RMVar_hsa_circ_291954,RMVar_hsa_circ_301302,RMVar_hsa_circ_326957,RMVar_hsa_circ_267594,RMVar_hsa_circ_25808,RMVar_hsa_circ_8027,RMVar_hsa_circ_228109,RMVar_hsa_circ_228111,RMVar_hsa_circ_228110,RMVar_hsa_circ_342746,RMVar_hsa_circ_51597,RMVar_hsa_circ_228113,RMVar_hsa_circ_228114 52577 RMVar_ID_52577 Human_SNP_ID_853776524 A-to-I Human chr4 - 118279068 118279068 118279068 CACAAGAGCGACAGAGTAGACTCAAGATGGCCACATGACACAGACGGCTGAACAGGCTTCACCGG CACAAGAGCGACAGAGTAGACTCAAGATGGCCGCATGACACAGACGGCTGAACAGGCTTCACCGG T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr4:118279068..118279069 30559470 RNA-Seq:(High) - Functional Loss SNV TCGA 33..33 33 UCEC 1 - RMVar_hsa_circ_228190,RMVar_hsa_circ_228191 52578 RMVar_ID_52578 Human_SNP_ID_853783085 A-to-I Human chr4 + 2833829 2833829 2833829 TGCTGCGGCACCCCTACGGCTACACTGGGCCTAGGTGATGGCAGTCCATGTGGCTGCCAGGCCAA TGCTGCGGCACCCCTACGGCTACACTGGGCCTGGGTGATGGCAGTCCATGTGGCTGCCAGGCCAA A G SH3BP2 Ensembl:ENSG00000087266 Protein coding CDS GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr4:2833828..2833829 24183664,29129909 RNA-Seq:(High) rs11542558 Functional Loss SNV COSMIC 33..33 33 bile_duct adenocarcinoma,biliary_tract adenocarcinoma 6 biliary tract,gallbladder RMVar_hsa_circ_89980,RMVar_hsa_circ_224397 52579 RMVar_ID_52579 Human_SNP_ID_853839997 A-to-I Human chr4 - 151126191 151126191 151126191 CCGAGCAACAGTGGCTCACACCTCTAATCCCAACACTTTTGGGAAGTCAAGGCAGGAGGATCGCT CCGAGCAACAGTGGCTCACACCTCTAATCCCATCACTTTTGGGAAGTCAAGGCAGGAGGATCGCT T A SH3D19 Ensembl:ENSG00000109686 Protein coding intron GSE100210 HepG2 cell line chr4:151126190..151126191 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_229133,RMVar_hsa_circ_120125,RMVar_hsa_circ_77723,RMVar_hsa_circ_229132 52580 RMVar_ID_52580 Human_SNP_ID_853946154 A-to-I Human chr4 - 13603149 13603149 13603149 GAATGTTACTGAGTGCCCCATCAGAAAATGATAGGGTACAGAAGAATTTGAAAAACACAGCTGCT GAATGTTACTGAGTGCCCCATCAGAAAATGATGGGGTACAGAAGAATTTGAAAAACACAGCTGCT T C BOD1L1 Ensembl:ENSG00000038219 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector chr4:13603148..13603149 29967493 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 stomach adenocarcinoma 1 stomach RMVar_hsa_circ_91864,RMVar_hsa_circ_224876,RMVar_hsa_circ_101305,RMVar_hsa_circ_224880,RMVar_hsa_circ_265090 52581 RMVar_ID_52581 Human_SNP_ID_853986041 A-to-I Human chr4 - 121370144 121370144 121370144 CAGTGATTTCAGAGCACAAGTATCAGCACCTCACCAAGGTGGAGGAAGGAGAGGCCAGTCTACCC CAGTGATTTCAGAGCACAAGTATCAGCACCTCGCCAAGGTGGAGGAAGGAGAGGCCAGTCTACCC T C AC093816.1,QRFPR Ensembl:ENSG00000213480,Ensembl:ENSG00000186867 Pseudogene,Protein coding exon,intron GSE100210 HepG2 cell line chr4:121370143..121370144 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue Human_RBP_ID_22401608 52582 RMVar_ID_52582 Human_SNP_ID_854039093 A-to-I Human chr4 + 2879709 2879709 2879709 CAGTGGCGTGATCTCGGCTCACTGTAGCCTCCACCTCCCGAGTTCAAATGATTCTCCTGCCTCAG CAGTGGCGTGATCTCGGCTCACTGTAGCCTCCCCCTCCCGAGTTCAAATGATTCTCCTGCCTCAG A C ADD1 Ensembl:ENSG00000087274 Protein coding intron GSE100210 HepG2 cell line chr4:2879708..2879709 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_15137652 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_224404 52583 RMVar_ID_52583 Human_SNP_ID_854131589 A-to-I Human chr4 - 169003517 169003517 169003517 TGCTATTGCTTTATCAACTAAGTTTATAGGATATTCTAAATCCTTTGTCATTTCTTTCAACAGTA TGCTATTGCTTTATCAACTAAGTTTATAGGATGTTCTAAATCCTTTGTCATTTCTTTCAACAGTA T C CBR4 Ensembl:ENSG00000145439 Protein coding intron GSE38233 cultured B-cells chr4:169003516..169003517 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_85493,RMVar_hsa_circ_121078,RMVar_hsa_circ_229488,RMVar_hsa_circ_272637,RMVar_hsa_circ_229489,RMVar_hsa_circ_366223,RMVar_hsa_circ_229491,RMVar_hsa_circ_229492 52584 RMVar_ID_52584 Human_SNP_ID_854459227 A-to-I Human chr4 - 21693388 21693388 21693388 CTCTGCTAATTTTTGTATTTTTACTAGAGACGAGGTTTCGCCATGTTGGCCAGGCTGGTCTTGAA CTCTGCTAATTTTTGTATTTTTACTAGAGACGGGGTTTCGCCATGTTGGCCAGGCTGGTCTTGAA T C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank chr4:21693387..21693388 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_16582,RMVar_hsa_circ_225086 52585 RMVar_ID_52585 Human_SNP_ID_854509244 A-to-I Human chr4 - 124212088 124212088 124212088 GGAATGCAATGGCGCAATCTGGGCTCACTGCAACCTCCGCCTCCCGGGTTCAAGCGATTCTCCTG GGAATGCAATGGCGCAATCTGGGCTCACTGCAGCCTCCGCCTCCCGGGTTCAAGCGATTCTCCTG T C AC121154.1 Ensembl:ENSG00000249837 lincRNA intron GSE100210 HepG2 cell line chr4:124212087..124212088 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 52586 RMVar_ID_52586 Human_SNP_ID_854568124 A-to-I Human chr4 - 113454475 113454475 113454475 CAACAGTGCCACTTCTGCATTCTCTGTTCTCAAGGCACCTGGATGGTGACCCTGGGCCGTCCTCT CAACAGTGCCACTTCTGCATTCTCTGTTCTCAGGGCACCTGGATGGTGACCCTGGGCCGTCCTCT T C CAMK2D Ensembl:ENSG00000145349 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector chr4:113454474..113454475 29967493 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_25829462 Human_Splice_Rec_600270,Human_Splice_Rec_600310,Human_Splice_Rec_600344,Human_Splice_Rec_600358,Human_Splice_Rec_600394 Human_miRNA_ID_1794833 52587 RMVar_ID_52587 Human_SNP_ID_854744564 A-to-I Human chr4 - 2938299 2938299 2938299 TCAGGCTGGTCTCGAATTCCCGACCTCAGGTAATCCACCTGCCTTGGCCCCCCAATTATAGGTGT TCAGGCTGGTCTCGAATTCCCGACCTCAGGTAGTCCACCTGCCTTGGCCCCCCAATTATAGGTGT T C NOP14 Ensembl:ENSG00000087269 Protein coding exon GSE38233;GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line chr4:2938298..2938299 24183664,29129909,32596459,32596459 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 rectum adenocarcinoma,LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia,large_intestine adenocarcinoma 14 large intestine,haematopoietic and lymphoid tissue Human_RBP_ID_26518016 Human_Splice_Rec_541082 Human_miRNA_ID_1119226,Human_miRNA_ID_1126365 52588 RMVar_ID_52588 Human_SNP_ID_854759015 A-to-I Human chr4 + 127659127 127659127 127659127 TCAGGCAATAATGTGAGTGATGGGGAGTGGCTATAAATATGAATGAAGCTTCGCTCACTGGCCAC TCAGGCAATAATGTGAGTGATGGGGAGTGGCTCTAAATATGAATGAAGCTTCGCTCACTGGCCAC A C INTU Ensembl:ENSG00000164066 Protein coding intron GSE100210 HepG2 cell line chr4:127659126..127659127 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_228492,RMVar_hsa_circ_267671,RMVar_hsa_circ_272662,RMVar_hsa_circ_327352,RMVar_hsa_circ_271026,RMVar_hsa_circ_41279,RMVar_hsa_circ_228490,RMVar_hsa_circ_228491,RMVar_hsa_circ_228489,RMVar_hsa_circ_19069,RMVar_hsa_circ_333852,RMVar_hsa_circ_228493 52589 RMVar_ID_52589 Human_SNP_ID_854825873 A-to-I Human chr4 - 75656968 75656968 75656968 TAAATTTTATGTTCACAATGATATGTTTCGTTATGAAGATGAAGTGTTTGGTGATTCTGAGCCTG TAAATTTTATGTTCACAATGATATGTTTCGTTTTGAAGATGAAGTGTTTGGTGATTCTGAGCCTG T A G3BP2 Ensembl:ENSG00000138757 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector chr4:75656967..75656968 29967493 RNA-Seq:(High) - Functional Loss SNV TCGA 33..33 33 LUAD 1 - Human_RBP_ID_71512,Human_RBP_ID_1640383,Human_RBP_ID_1980947,Human_RBP_ID_9396415,Human_RBP_ID_15199835,Human_RBP_ID_22458631,Human_RBP_ID_22826454,Human_RBP_ID_24064308,Human_RBP_ID_26694967 Human_Splice_Rec_569894,Human_Splice_Rec_569895,Human_Splice_Rec_569916,Human_Splice_Rec_569917,Human_Splice_Rec_569938,Human_Splice_Rec_569939,Human_Splice_Rec_569954,Human_Splice_Rec_569955,Human_Splice_Rec_569972,Human_Splice_Rec_569973,Human_Splice_Rec_569982,Human_Splice_Rec_569983,Human_Splice_Rec_569992,Human_Splice_Rec_569998,Human_Splice_Rec_570006 RMVar_hsa_circ_18997,RMVar_hsa_circ_282608,RMVar_hsa_circ_57123,RMVar_hsa_circ_226620,RMVar_hsa_circ_226621,RMVar_hsa_circ_314485,RMVar_hsa_circ_28236,RMVar_hsa_circ_16196,RMVar_hsa_circ_286799,RMVar_hsa_circ_30296,RMVar_hsa_circ_308649,RMVar_hsa_circ_226626,RMVar_hsa_circ_321574,RMVar_hsa_circ_226627 52590 RMVar_ID_52590 Human_SNP_ID_854848127 A-to-I Human chr4 + 128017017 128017017 128017017 TCAGCTCACTGCAGCCTCTGCCTCCCAGGTTCAAGCGATTTTCATGCCTCAGTTTTCCACGTAGC TCAGCTCACTGCAGCCTCTGCCTCCCAGGTTCTAGCGATTTTCATGCCTCAGTTTTCCACGTAGC A T ABHD18 Ensembl:ENSG00000164074 Protein coding intron GSE100210 HepG2 cell line chr4:128017017..128017018 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 6 ovary RMVar_hsa_circ_6941,RMVar_hsa_circ_279023,RMVar_hsa_circ_288390,RMVar_hsa_circ_300769,RMVar_hsa_circ_287896,RMVar_hsa_circ_38832,RMVar_hsa_circ_228537,RMVar_hsa_circ_228539,RMVar_hsa_circ_228540,RMVar_hsa_circ_228538,RMVar_hsa_circ_369134,RMVar_hsa_circ_228546,RMVar_hsa_circ_321824,RMVar_hsa_circ_228549,RMVar_hsa_circ_307927,RMVar_hsa_circ_326565,RMVar_hsa_circ_228547,RMVar_hsa_circ_68990,RMVar_hsa_circ_305903,RMVar_hsa_circ_228550,RMVar_hsa_circ_228551,RMVar_hsa_circ_228548 52591 RMVar_ID_52591 Human_SNP_ID_855053805 A-to-I Human chr4 + 39752202 39752202 39752202 TCCCCCAGGCTGGAGTGCAGTGGCACGATCTCAGCTCACTGCAAGCTCCATCTCCCTTTACGCCA TCCCCCAGGCTGGAGTGCAGTGGCACGATCTCGGCTCACTGCAAGCTCCATCTCCCTTTACGCCA A G UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE100210 HepG2 cell line chr4:39752201..39752202 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - RMVar_hsa_circ_225460,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_225472,RMVar_hsa_circ_271227,RMVar_hsa_circ_225471,RMVar_hsa_circ_225476,RMVar_hsa_circ_225474,RMVar_hsa_circ_287533,RMVar_hsa_circ_313227,RMVar_hsa_circ_289256,RMVar_hsa_circ_225475,RMVar_hsa_circ_225473 52592 RMVar_ID_52592 Human_SNP_ID_855275357 A-to-I Human chr4 - 6472171 6472171 6472171 AATTAACCACAGCTTCCTGCGGGACCACAGCTATGTGACTGAAGGTAACGTACGTGTTGTCTGAG AATTAACCACAGCTTCCTGCGGGACCACAGCTGTGTGACTGAAGGTAACGTACGTGTTGTCTGAG T C PPP2R2C Ensembl:ENSG00000074211 Protein coding CDS GSE47997 K562 cells&HepG2 cells chr4:6472170..6472171 23474544 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 READ,rectum adenocarcinoma,large_intestine adenocarcinoma 5 large intestine Human_RBP_ID_4788334 Human_Splice_Rec_543661 RMVar_hsa_circ_276581 52593 RMVar_ID_52593 Human_SNP_ID_855310433 A-to-I Human chr4 + 151456248 151456248 151456248 CCGAAAGTCTATCCATTGAAAAGGTTCTTTTTAAAATAACATCAGCTTTCAGTACTCTAAAATGA CCGAAAGTCTATCCATTGAAAAGGTTCTTTTTGAAATAACATCAGCTTTCAGTACTCTAAAATGA A G FAM160A1 Ensembl:ENSG00000164142 Protein coding intron GSE100210 HepG2 cell line chr4:151456247..151456248 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_58110,RMVar_hsa_circ_229144,RMVar_hsa_circ_361940,RMVar_hsa_circ_320247,RMVar_hsa_circ_229145 52594 RMVar_ID_52594 Human_SNP_ID_855351315 A-to-I Human chr4 - 673825 673825 673825 TCCTGTGCTATTTGGAGAACTCCAGCTCTGGAAGGGGGCTTGGGACGCATGCGAGGCTGCAGGAC TCCTGTGCTATTTGGAGAACTCCAGCTCTGGAGGGGGGCTTGGGACGCATGCGAGGCTGCAGGAC T C ATP5ME Ensembl:ENSG00000169020 Protein coding intron GSE100210 HepG2 cell line chr4:673824..673825 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 CHOL 1 - RMVar_hsa_circ_83130,RMVar_hsa_circ_103935,RMVar_hsa_circ_224182,RMVar_hsa_circ_224183 52595 RMVar_ID_52595 Human_SNP_ID_855397408 A-to-I Human chr4 - 21506900 21506900 21506900 GTAGTCCCATCTACTTGGGAGGCTGAGACAGAAGGATTGCTTTGGCCCAGGAGTTTGAGGCTGCA GTAGTCCCATCTACTTGGGAGGCTGAGACAGACGGATTGCTTTGGCCCAGGAGTTTGAGGCTGCA T G KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,cerebellum chr4:21506899..21506900 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_16582 52596 RMVar_ID_52596 Human_SNP_ID_855447836 A-to-I Human chr4 - 39973818 39973818 39973818 CCCGGTCTTGCAGCACGGTTCTGAGTCTGTGGAATAGCTGCCATGAAGTAACCTGAAGGAGGTGC CCCGGTCTTGCAGCACGGTTCTGAGTCTGTGGGATAGCTGCCATGAAGTAACCTGAAGGAGGTGC T C PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE100210 HepG2 cell line chr4:39973817..39973818 29129909 RNA-Seq:(High) rs878904637 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 haematopoietic and lymphoid tissue Human_RBP_ID_15152020 RMVar_hsa_circ_118437,RMVar_hsa_circ_225482,RMVar_hsa_circ_115099,RMVar_hsa_circ_101014,RMVar_hsa_circ_225524,RMVar_hsa_circ_225525,RMVar_hsa_circ_52264,RMVar_hsa_circ_62955,RMVar_hsa_circ_5363 52597 RMVar_ID_52597 Human_SNP_ID_855476936 A-to-I Human chr4 + 87892503 87892503 87892503 CTATCCCATCACCCTTTATTTGGAGAAGGAACAAGACAAGGAAATTAGTGATGATGAGGCAGAAG CTATCCCATCACCCTTTATTTGGAGAAGGAACGAGACAAGGAAATTAGTGATGATGAGGCAGAAG A G HSP90AB3P Ensembl:ENSG00000183199 Pseudogene exon GSE100210 HepG2 cell line chr4:87892502..87892503 29129909 RNA-Seq:(High) rs879027927 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_3749892 52598 RMVar_ID_52598 Human_SNP_ID_855599378 A-to-I Human chr4 - 21507450 21507450 21507450 GAGTTCGAGACCAGCCTGGGCAACACGGTCAAACCCTGTCTCTACTAAAAATTAGCTGGTCGTGT GAGTTCGAGACCAGCCTGGGCAACACGGTCAATCCCTGTCTCTACTAAAAATTAGCTGGTCGTGT T A KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,frontal_cortex chr4:21507449..21507450 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_16582 52599 RMVar_ID_52599 Human_SNP_ID_855623301 A-to-I Human chr4 - 21781292 21781292 21781292 AGGAGGCCTCAGGAAACTTAAATTATGGCAGAAGGTGAAAGGGAAACAAGGACCTTCTTCACAGG AGGAGGCCTCAGGAAACTTAAATTATGGCAGACGGTGAAAGGGAAACAAGGACCTTCTTCACAGG T G KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,cerebellum chr4:21781291..21781292 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 52600 RMVar_ID_52600 Human_SNP_ID_855666273 A-to-I Human chr4 + 86971984 86971984 86971984 CAAAGTGAGACTCCATCTCTACAAAAACTTCAAAAGATTAGTCGGGAATAGTGGCACATGCCTGT CAAAGTGAGACTCCATCTCTACAAAAACTTCACAAGATTAGTCGGGAATAGTGGCACATGCCTGT A C AFF1 Ensembl:ENSG00000172493 Protein coding intron GSE100210 HepG2 cell line chr4:86971984..86971985 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 oesophagus adenocarcinoma 1 oesophagus RMVar_hsa_circ_355934,RMVar_hsa_circ_365059,RMVar_hsa_circ_227318,RMVar_hsa_circ_311450 52601 RMVar_ID_52601 Human_SNP_ID_855693203 A-to-I Human chr4 - 2938735 2938735 2938735 GGGAGGCCAAGGCAGGAAGATTGCTTCAGCCCAGGAGTTCGAGACCAGCCTGGGCAACACAGGAA GGGAGGCCAAGGCAGGAAGATTGCTTCAGCCCGGGAGTTCGAGACCAGCCTGGGCAACACAGGAA T C NOP14 Ensembl:ENSG00000087269 Protein coding intron GSE38233;GSE100210;GSE99789;GSE112787;GSE107867;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;293 Flip-In T-REx cells,empty vector;ASD brains,cerebellum;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line chr4:2938734..2938735 24183664,29129909,29796672,29967493,30559470,32596459,32596459 RNA-Seq:(High) rs1456204463 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 5 haematopoietic and lymphoid tissue Human_RBP_ID_4799170,Human_RBP_ID_22291194,Human_RBP_ID_22826081,Human_RBP_ID_25806236,Human_RBP_ID_27067431 52602 RMVar_ID_52602 Human_SNP_ID_855778566 A-to-I Human chr4 - 48096704 48096703 48096704 GCCAACACGGTGAAACCTTGTCTCCACAAAAAATACAAAAATTAGCCAGGCATGGTGGCATGTGC GCCAACACGGTGAAACCTTGTCTCCACAAAAA_TACAAAAATTAGCCAGGCATGGTGGCATGTGC AT A TXK Ensembl:ENSG00000074966 Protein coding intron GSE47997 K562 cells&HepG2 cells chr4:48096703..48096704 23474544 RNA-Seq:(High) - Functional Loss DEL ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_3742,RMVar_hsa_circ_53343,RMVar_hsa_circ_62737,RMVar_hsa_circ_71237,RMVar_hsa_circ_360652,RMVar_hsa_circ_65811,RMVar_hsa_circ_53473,RMVar_hsa_circ_116485,RMVar_hsa_circ_358015,RMVar_hsa_circ_225895 52603 RMVar_ID_52603 Human_SNP_ID_855823205 A-to-I Human chr4 + 127839536 127839536 127839536 CTTGAACCCTGGCGAAACCCCATTTCTAAAATAGAAAAATTTAGCCGGGTGTGGTGGTGTGTGCC CTTGAACCCTGGCGAAACCCCATTTCTAAAATGGAAAAATTTAGCCGGGTGTGGTGGTGTGTGCC A G HSPA4L Ensembl:ENSG00000164070 Protein coding 3'UTR GSE100210 HepG2 cell line chr4:127839535..127839536 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma,CLLE 2 haematopoietic and lymphoid tissue 52604 RMVar_ID_52604 Human_SNP_ID_855998708 A-to-I Human chr4 - 98615691 98615691 98615691 TCAGCCTCCTGAGTAGCTGGGATTACAGGCATACATTACCACGCCCTGCTAATTTTGGTATTTTT TCAGCCTCCTGAGTAGCTGGGATTACAGGCATGCATTACCACGCCCTGCTAATTTTGGTATTTTT T C TSPAN5 Ensembl:ENSG00000168785 Protein coding intron GSE107867 ASD brains,cerebellum chr4:98615690..98615691 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_121310,RMVar_hsa_circ_227622 52605 RMVar_ID_52605 Human_SNP_ID_856042727 A-to-I Human chr4 + 48856548 48856548 48856548 AGTTAGGATTACAGGTGTGTGCCACCACGCCCAACTAATTTTGTGTTTTTAGTAGAGATGAGGTT AGTTAGGATTACAGGTGTGTGCCACCACGCCCCACTAATTTTGTGTTTTTAGTAGAGATGAGGTT A C OCIAD1 Ensembl:ENSG00000109180 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr4:48856548..48856549 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - RMVar_hsa_circ_269179,RMVar_hsa_circ_281679,RMVar_hsa_circ_225985,RMVar_hsa_circ_225986,RMVar_hsa_circ_296033,RMVar_hsa_circ_225987,RMVar_hsa_circ_324043,RMVar_hsa_circ_225989,RMVar_hsa_circ_286205,RMVar_hsa_circ_225990 52606 RMVar_ID_52606 Human_SNP_ID_856063694 A-to-I Human chr4 + 2703350 2703350 2703350 CTCACTGCATCCTCCACCCCCCAGGTTGAAGCAATTCTCCCACCTCAGCCTCCCAAGTAGCTGAA CTCACTGCATCCTCCACCCCCCAGGTTGAAGCTATTCTCCCACCTCAGCCTCCCAAGTAGCTGAA A T FAM193A Ensembl:ENSG00000125386 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr4:2703349..2703350 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_68554,RMVar_hsa_circ_75128,RMVar_hsa_circ_67890,RMVar_hsa_circ_65572,RMVar_hsa_circ_307706,RMVar_hsa_circ_224373,RMVar_hsa_circ_38026,RMVar_hsa_circ_56234,RMVar_hsa_circ_268752,RMVar_hsa_circ_62263,RMVar_hsa_circ_348051,RMVar_hsa_circ_224385,RMVar_hsa_circ_296555,RMVar_hsa_circ_224386 52607 RMVar_ID_52607 Human_SNP_ID_856095894 A-to-I Human chr4 - 21101193 21101193 21101193 AGCAAGTCAAATACCACATATTCTCACTTATAAGTGGGAGCTGAACAATGCGTACAGATGGACAT AGCAAGTCAAATACCACATATTCTCACTTATAGGTGGGAGCTGAACAATGCGTACAGATGGACAT T C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,temporal_cortex chr4:21101192..21101193 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_16582 52608 RMVar_ID_52608 Human_SNP_ID_856269380 A-to-I Human chr4 - 39961593 39961593 39961593 GCTCTGTAGTTCCAGACCAGCTTGGGCAAAATAGTGAGACCCAGACTCTATTAAAAAGGAAAGAT GCTCTGTAGTTCCAGACCAGCTTGGGCAAAATTGTGAGACCCAGACTCTATTAAAAAGGAAAGAT T A PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE38233 cultured B-cells chr4:39961592..39961593 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_118437,RMVar_hsa_circ_225482,RMVar_hsa_circ_115099,RMVar_hsa_circ_101014,RMVar_hsa_circ_225524,RMVar_hsa_circ_225525,RMVar_hsa_circ_52264,RMVar_hsa_circ_62955,RMVar_hsa_circ_5363 52609 RMVar_ID_52609 Human_SNP_ID_856285367 A-to-I Human chr4 - 21798633 21798633 21798633 AGCTTAACAGCTTATTTTTTTCTCATTCTCTTAATCTATTGGAGAATAGCTTAAAAGAGTGGCTC AGCTTAACAGCTTATTTTTTTCTCATTCTCTTCATCTATTGGAGAATAGCTTAAAAGAGTGGCTC T G KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,frontal_cortex chr4:21798632..21798633 30559470 RNA-Seq:(High) rs1283748381 Functional Loss SNV ICGC 33..33 33 ESCA 1 - 52610 RMVar_ID_52610 Human_SNP_ID_856287584 A-to-I Human chr4 + 39772833 39772833 39772833 CCTCAGCCACCTGAGCAGCTGGGATTACAGGCACATGCCACCACGCCCAGCTAATTTTTGCATTT CCTCAGCCACCTGAGCAGCTGGGATTACAGGCTCATGCCACCACGCCCAGCTAATTTTTGCATTT A T UBE2K Ensembl:ENSG00000078140 Protein coding intron GSE38233 cultured B-cells chr4:39772832..39772833 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_225460,RMVar_hsa_circ_225465,RMVar_hsa_circ_225464,RMVar_hsa_circ_225459,RMVar_hsa_circ_225463,RMVar_hsa_circ_225468,RMVar_hsa_circ_298369,RMVar_hsa_circ_225467,RMVar_hsa_circ_225472,RMVar_hsa_circ_271227,RMVar_hsa_circ_225471,RMVar_hsa_circ_225476,RMVar_hsa_circ_225474,RMVar_hsa_circ_287533,RMVar_hsa_circ_313227,RMVar_hsa_circ_225473,RMVar_hsa_circ_225477,RMVar_hsa_circ_279938,RMVar_hsa_circ_280268,RMVar_hsa_circ_225478 52611 RMVar_ID_52611 Human_SNP_ID_856372046 A-to-I Human chr4 + 176320174 176320174 176320174 CACCTTCGGCTGCTTCATCACCACCGCCTTCAAAGACAGGAGCGTCCCGGTGCGGCTGCACGTCT CACCTTCGGCTGCTTCATCACCACCGCCTTCATAGACAGGAGCGTCCCGGTGCGGCTGCACGTCT A T SPCS3 Ensembl:ENSG00000129128 Protein coding CDS GSE100210 HepG2 cell line chr4:176320174..176320175 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 ovary serous_carcinoma 1 ovary Human_RBP_ID_71244,Human_RBP_ID_248971,Human_RBP_ID_4794762,Human_RBP_ID_9396800,Human_RBP_ID_22095744,Human_RBP_ID_22458061 Human_Splice_Rec_624641,Human_Splice_Rec_624651 RMVar_hsa_circ_100028,RMVar_hsa_circ_229639 52612 RMVar_ID_52612 Human_SNP_ID_856464128 A-to-I Human chr4 + 108623557 108623557 108623557 TCAGCCTCCTGAATAGCTGGGACTGCAGGCACATGCCACCACACTTGACTGATTTTTTGTATTTT TCAGCCTCCTGAATAGCTGGGACTGCAGGCACGTGCCACCACACTTGACTGATTTTTTGTATTTT A G RPL34 Ensembl:ENSG00000109475 Protein coding intron GSE100210 HepG2 cell line chr4:108623556..108623557 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - RMVar_hsa_circ_356074 52613 RMVar_ID_52613 Human_SNP_ID_856492545 A-to-I Human chr4 - 21924486 21924486 21924486 TAATCCCAGCACTTTGGGAGGCCGAGACGGACAGATCATGAGGTCAGCAGATAGAGACCATTTTG TAATCCCAGCACTTTGGGAGGCCGAGACGGACCGATCATGAGGTCAGCAGATAGAGACCATTTTG T G KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank chr4:21924485..21924486 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 3 pancreas 52614 RMVar_ID_52614 Human_SNP_ID_856533191 A-to-I Human chr4 - 3525001 3525001 3525001 AGGCTGGCCGAGCTCCACGCTGATCTGAAGATACAGGAGAGGGACGAACTCGCCTGGAAGAAACT AGGCTGGCCGAGCTCCACGCTGATCTGAAGATGCAGGAGAGGGACGAACTCGCCTGGAAGAAACT T C LRPAP1 Ensembl:ENSG00000163956 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector chr4:3525000..3525001 29967493 RNA-Seq:(High) - 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 52615 RMVar_ID_52615 Human_SNP_ID_856535512 A-to-I Human chr4 - 21030996 21030996 21030996 GGGTTGCTTCTATGCCATGCTCTCTCCTTTGAAGGTGTTTCTCTGGGCCTGGGGAACACCCTCAA GGGTTGCTTCTATGCCATGCTCTCTCCTTTGAGGGTGTTTCTCTGGGCCTGGGGAACACCCTCAA T C KCNIP4 Ensembl:ENSG00000185774 Protein coding intron GSE107867 ASD brains,temporal_cortex chr4:21030995..21030996 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 STAD 1 - RMVar_hsa_circ_16582 52616 RMVar_ID_52616 Human_SNP_ID_856547341 A-to-I Human chr4 - 39953559 39953559 39953559 ACCCAGCTACAATTTAAATTTTTAGTAGAGACAAGGTCTCACTATGTTTTCCAGGCTGGTCTTAA ACCCAGCTACAATTTAAATTTTTAGTAGAGACGAGGTCTCACTATGTTTTCCAGGCTGGTCTTAA T C PDS5A Ensembl:ENSG00000121892 Protein coding intron GSE47997 K562 cells&HepG2 cells chr4:39953558..39953559 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 3 pancreas RMVar_hsa_circ_118437,RMVar_hsa_circ_225482,RMVar_hsa_circ_115099,RMVar_hsa_circ_101014,RMVar_hsa_circ_225524,RMVar_hsa_circ_225525,RMVar_hsa_circ_52264,RMVar_hsa_circ_62955,RMVar_hsa_circ_5363 52617 RMVar_ID_52617 Human_SNP_ID_856629688 A-to-I Human chr4 - 36099132 36099132 36099132 AGAAAACCAGACACCGCATGTTCTCGCTTATAAGTGGGAGCCGAATGATGAGAACATATGGACAC AGAAAACCAGACACCGCATGTTCTCGCTTATAGGTGGGAGCCGAATGATGAGAACATATGGACAC T C ARAP2 Ensembl:ENSG00000047365 Protein coding intron GSE107867 ASD brains,frontal_cortex chr4:36099131..36099132 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 STAD 1 - RMVar_hsa_circ_29356,RMVar_hsa_circ_5935,RMVar_hsa_circ_68837,RMVar_hsa_circ_266800,RMVar_hsa_circ_55667,RMVar_hsa_circ_66330,RMVar_hsa_circ_286290,RMVar_hsa_circ_345268,RMVar_hsa_circ_268780,RMVar_hsa_circ_49632,RMVar_hsa_circ_225289 52618 RMVar_ID_52618 Human_SNP_ID_856647266 A-to-I Human chr4 + 7582601 7582601 7582601 TTTCATATGTAGCAGAGCAGCTCCCTCGCTGCAATCTATTGAAAGTCAGCCCTCGACACAAGGGT TTTCATATGTAGCAGAGCAGCTCCCTCGCTGCGATCTATTGAAAGTCAGCCCTCGACACAAGGGT A G SORCS2 Ensembl:ENSG00000184985 Protein coding intron GSE100210 HepG2 cell line chr4:7582600..7582601 29129909 RNA-Seq:(High) rs75476276 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 4 brain Human_RBP_ID_72998,Human_RBP_ID_163499,Human_RBP_ID_270578,Human_RBP_ID_1107774,Human_RBP_ID_1139756,Human_RBP_ID_1209239,Human_RBP_ID_1317646,Human_RBP_ID_1641952,Human_RBP_ID_1980871,Human_RBP_ID_2871024,Human_RBP_ID_5276251,Human_RBP_ID_5301010,Human_RBP_ID_8265856,Human_RBP_ID_8594534,Human_RBP_ID_9162754,Human_RBP_ID_9341463,Human_RBP_ID_10154701,Human_RBP_ID_15198215,Human_RBP_ID_17671523,Human_RBP_ID_17706129,Human_RBP_ID_18029250,Human_RBP_ID_18471849,Human_RBP_ID_18517760,Human_RBP_ID_18537630,Human_RBP_ID_18828376,Human_RBP_ID_19123360,Human_RBP_ID_20977573,Human_RBP_ID_21898974,Human_RBP_ID_22293072,Human_RBP_ID_22401948,Human_RBP_ID_22458135,Human_RBP_ID_22826764,Human_RBP_ID_23033531,Human_RBP_ID_23191233,Human_RBP_ID_23313633,Human_RBP_ID_24063923,Human_RBP_ID_24430367,Human_RBP_ID_24547763,Human_RBP_ID_25820366,Human_RBP_ID_26516714,Human_RBP_ID_26694913,Human_RBP_ID_27070011,Human_RBP_ID_27160171,Human_RBP_ID_27328495 52619 RMVar_ID_52619 Human_SNP_ID_856660718 A-to-I Human chr4 - 13336979 13336979 13336979 ACCCCTACCAATAGGCTCACCATGGTCAGCACACACAGTGAAGGAACCTCCAGCAGAAGACTCTC ACCCCTACCAATAGGCTCACCATGGTCAGCACGCACAGTGAAGGAACCTCCAGCAGAAGACTCTC T C lnc-RAB28-5 RNACentral:URS00008B7EF7 lincRNA intron GSE100210 HepG2 cell line chr4:13336978..13336979 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA 33..33 33 COAD 1 - RMVar_hsa_circ_97367,RMVar_hsa_circ_224858,RMVar_hsa_circ_224859,RMVar_hsa_circ_224860 52620 RMVar_ID_52620 Human_SNP_ID_856664841 A-to-I Human chr4 - 10081421 10081421 10081421 CTCTAACAGCGGACAAGGAGTTGTGAAACTGGACGTTCAGCCAAAGTGCGTAGCCGTCGGCCCCG CTCTAACAGCGGACAAGGAGTTGTGAAACTGGGCGTTCAGCCAAAGTGCGTAGCCGTCGGCCCCG T C WDR1 Ensembl:ENSG00000071127 Protein coding CDS GSE100210 HepG2 cell line chr4:10081420..10081421 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 6 uterus Human_RBP_ID_70707,Human_RBP_ID_3966149,Human_RBP_ID_8876134,Human_RBP_ID_22510042 Human_Splice_Rec_545820,Human_Splice_Rec_545821,Human_Splice_Rec_545840,Human_Splice_Rec_545841,Human_Splice_Rec_545866,Human_Splice_Rec_545867,Human_Splice_Rec_545884,Human_Splice_Rec_545885,Human_Splice_Rec_545906,Human_Splice_Rec_545907,Human_Splice_Rec_545924,Human_Splice_Rec_545925 Human_miRNA_ID_2069715,Human_miRNA_ID_2802617 RMVar_hsa_circ_8901,RMVar_hsa_circ_94689,RMVar_hsa_circ_127946,RMVar_hsa_circ_111272,RMVar_hsa_circ_122269,RMVar_hsa_circ_224830,RMVar_hsa_circ_224831,RMVar_hsa_circ_224829,RMVar_hsa_circ_16319,RMVar_hsa_circ_71998,RMVar_hsa_circ_224834,RMVar_hsa_circ_269024,RMVar_hsa_circ_29883 52621 RMVar_ID_52621 Human_SNP_ID_832235127 A-to-I Human chr19 - 10169644 10169644 10169644 CTCCTGCCTCAGCCTCCCGAGTAACTGGGACTACAGGCACCTGCTACCACGCCAGGCTAATTTTT CTCCTGCCTCAGCCTCCCGAGTAACTGGGACTGCAGGCACCTGCTACCACGCCAGGCTAATTTTT T C DNMT1 Ensembl:ENSG00000130816 Protein coding intron GSE100210 HepG2 cell line chr19:10169643..10169644 29129909 RNA-Seq:(High) rs1422363956 Functional Loss SNV ICGC 33..33 33 MALY 1 - 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_378899,RMVar_hsa_circ_323045,RMVar_hsa_circ_61383,RMVar_hsa_circ_192310,RMVar_hsa_circ_364236,RMVar_hsa_circ_59709,RMVar_hsa_circ_303974,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_268592,RMVar_hsa_circ_192317 52622 RMVar_ID_52622 Human_SNP_ID_832241593 A-to-I Human chr19 - 4093434 4093434 4093434 CACCTGCCTCAGCCTCCCAAAGTGCAGAGATTACAGATGTGAGCCACCGCACCTGGTCAAAAAAA CACCTGCCTCAGCCTCCCAAAGTGCAGAGATTTCAGATGTGAGCCACCGCACCTGGTCAAAAAAA T A MAP2K2 Ensembl:ENSG00000126934 Protein coding intron GSE100210 HepG2 cell line chr19:4093433..4093434 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - RMVar_hsa_circ_96157,RMVar_hsa_circ_191493 52623 RMVar_ID_52623 Human_SNP_ID_832243991 A-to-I Human chr19 - 48743915 48743915 48743915 ACGATCACGGCTCACTGCAACCTCCACCTCCCAGGTTCAAACTATTCTCCTGCCTCAGCCCCCTG ACGATCACGGCTCACTGCAACCTCCACCTCCCGGGTTCAAACTATTCTCCTGCCTCAGCCCCCTG T C IZUMO1 Ensembl:ENSG00000182264 Protein coding intron GSE47997 K562 cells&HepG2 cells chr19:48743914..48743915 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 52624 RMVar_ID_52624 Human_SNP_ID_832251140 A-to-I Human chr19 - 55705858 55705858 55705858 AGCTTTAGTGATAGAGCAAGACCTTGTCTCTAAATATATATATATATCCCACAACACTCTAAATA AGCTTTAGTGATAGAGCAAGACCTTGTCTCTAGATATATATATATATCCCACAACACTCTAAATA T C - - Other Unknown GSE100210 HepG2 cell line chr19:55705857..55705858 29129909 RNA-Seq:(High) rs536467064 Functional Loss SNV ICGC 33..33 33 PBCA 2 - 52625 RMVar_ID_52625 Human_SNP_ID_832258488 A-to-I Human chr19 - 52031934 52031934 52031934 GGAGTGTAATAGCACGATCTTGGCTCACTGCAACCCCGCCTCCCAGGTTCAAGAGATTTTCCTGC GGAGTGTAATAGCACGATCTTGGCTCACTGCACCCCCGCCTCCCAGGTTCAAGAGATTTTCCTGC T G ZNF432 Ensembl:ENSG00000256087 Protein coding 3'UTR GSE100210 HepG2 cell line chr19:52031933..52031934 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 2 - 52626 RMVar_ID_52626 Human_SNP_ID_832263461 A-to-I Human chr19 + 37361818 37361818 37361818 GGACGCCTGTAATCCCAGCTACTCGGGAGGCTAAGGCAGGAGAATCGCTTGAACCCTGGAGGCGG GGACGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCTGGAGGCGG A G ZNF875 Ensembl:ENSG00000181666 Protein coding intron GSE47997 K562 cells&HepG2 cells chr19:37361817..37361818;chr19:37361818..37361819 23474544 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 10 prostate 52627 RMVar_ID_52627 Human_SNP_ID_832264319 A-to-I Human chr19 - 45388402 45388402 45388402 CCCAGATAATATTTAACATTTTCAGTAGAGACAGTTCTCATTATGTTGTCCAGGCTGGTCTCAAA CCCAGATAATATTTAACATTTTCAGTAGAGACCGTTCTCATTATGTTGTCCAGGCTGGTCTCAAA T G PPP1R13L Ensembl:ENSG00000104881 Protein coding intron GSE100210 HepG2 cell line chr19:45388401..45388402 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_12194,RMVar_hsa_circ_30152,RMVar_hsa_circ_105334,RMVar_hsa_circ_195339 52628 RMVar_ID_52628 Human_SNP_ID_832281242 A-to-I Human chr19 - 35887794 35887794 35887794 ACAATTGGCTGGACATGGTGGCATGCGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGAAGA ACAATTGGCTGGACATGGTGGCATGCGCCTGTTGTCCCAGCTACTTGGGAGGCTGAGGCAGAAGA T A NFKBID Ensembl:ENSG00000167604 Protein coding 3'UTR GSE100210 HepG2 cell line chr19:35887793..35887794 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 52629 RMVar_ID_52629 Human_SNP_ID_832320862 A-to-I Human chr19 + 52422148 52422148 52422148 TTTTTCAGGCTGAGTGGGGGTGGCTCACCTGTAATCTCAGCACTTCGGGAGGCCAAGGTGGGAGA TTTTTCAGGCTGAGTGGGGGTGGCTCACCTGTGATCTCAGCACTTCGGGAGGCCAAGGTGGGAGA A G - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr19:52422148..52422149 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 52630 RMVar_ID_52630 Human_SNP_ID_832322416 A-to-I Human chr19 + 35411209 35411209 35411209 GTTGCCCAGGCTGAAGTCAACGGCATGATCTCAGCTCACTGCAACCTCCACCTCCTGGGTTCAAG GTTGCCCAGGCTGAAGTCAACGGCATGATCTCGGCTCACTGCAACCTCCACCTCCTGGGTTCAAG A G LINC01531 Ensembl:ENSG00000205786 lincRNA exon GSE38233 cultured B-cells chr19:35411208..35411209 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_Splice_Rec_1993508,Human_Splice_Rec_1993509,Human_Splice_Rec_1993524,Human_Splice_Rec_1993530,Human_Splice_Rec_1993531,Human_Splice_Rec_1993536,Human_Splice_Rec_1993537,Human_Splice_Rec_1993540,Human_Splice_Rec_1993541 RMVar_hsa_circ_90402,RMVar_hsa_circ_194229 52631 RMVar_ID_52631 Human_SNP_ID_832322969 A-to-I Human chr19 - 52807577 52807577 52807577 CCAGCTCCTAGAGAGGCTGAGGAAAGAGAATTACTTGAACCCAGGAGGCCAAGTTTTGCATTGAG CCAGCTCCTAGAGAGGCTGAGGAAAGAGAATTTCTTGAACCCAGGAGGCCAAGTTTTGCATTGAG T A ZNF28 Ensembl:ENSG00000198538 Protein coding intron GSE38233 cultured B-cells chr19:52807576..52807577 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_128048,RMVar_hsa_circ_196171,RMVar_hsa_circ_117051,RMVar_hsa_circ_196174 52632 RMVar_ID_52632 Human_SNP_ID_832325295 A-to-I Human chr19 + 18345644 18345644 18345644 CTACTCGGGAGGCTAATATGGGAGGATCACCTAAGCCTGGGGAGGTAGAGGCTGCAGTGAGCCCT CTACTCGGGAGGCTAATATGGGAGGATCACCTTAGCCTGGGGAGGTAGAGGCTGCAGTGAGCCCT A T PGPEP1 Ensembl:ENSG00000130517 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line chr19:18345643..18345644;chr19:18345644..18345645 23474544,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 RECA 1 - RMVar_hsa_circ_108567,RMVar_hsa_circ_193465 52633 RMVar_ID_52633 Human_SNP_ID_832327760 A-to-I Human chr19 + 11441257 11441255 11441257 GTCTCCGCACCGCAGAGAGAAGGGCCGTAAGGAGAGAGAGTCCCTGCAGCAGATGGCCGAGGTCA GTCTCCGCACCGCAGAGAGAAGGGCCGTAAG__GAGAGAGTCCCTGCAGCAGATGGCCGAGGTCA GGA G PRKCSH Ensembl:ENSG00000130175 Protein coding CDS GSE100210 HepG2 cell line chr19:11441256..11441257 29129909 RNA-Seq:(High) rs779685748 Functional Loss DEL TCGA 32..33 33 STAD,UCEC 2 - Human_RBP_ID_771505,Human_RBP_ID_825089,Human_RBP_ID_912374,Human_RBP_ID_3954512,Human_RBP_ID_18470507,Human_RBP_ID_18722085,Human_RBP_ID_22447415,Human_RBP_ID_22533115,Human_RBP_ID_22762757,Human_RBP_ID_26334858,Human_RBP_ID_27463201 Human_Splice_Rec_1960668,Human_Splice_Rec_1960706,Human_Splice_Rec_1960722,Human_Splice_Rec_1960742,Human_Splice_Rec_1960752,Human_Splice_Rec_1960786,Human_Splice_Rec_1960794,Human_Splice_Rec_1960826 RMVar_hsa_circ_192595,RMVar_hsa_circ_346963 52634 RMVar_ID_52634 Human_SNP_ID_832333217 A-to-I Human chr19 - 45618692 45618692 45618692 CGCCCGCCTCGGCCTCTCAAAGTGCTGGGATTACAGATGCCAGCCACCAAGCCTGGCCCAAACAA CGCCCGCCTCGGCCTCTCAAAGTGCTGGGATTGCAGATGCCAGCCACCAAGCCTGGCCCAAACAA T C EML2 Ensembl:ENSG00000125746 Protein coding intron GSE100210 HepG2 cell line chr19:45618691..45618692 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_10744,RMVar_hsa_circ_372977,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_195377 52635 RMVar_ID_52635 Human_SNP_ID_832341732 A-to-I Human chr19 - 57906939 57906939 57906939 TGAGGCAGGAGAATTCGTTAAACCTGGGAGGCATAGGTTGCAGTGAGCCGAGATTGCACCACTGC TGAGGCAGGAGAATTCGTTAAACCTGGGAGGCGTAGGTTGCAGTGAGCCGAGATTGCACCACTGC T C ZNF417,AC010326.2 Ensembl:ENSG00000173480,Ensembl:ENSG00000269476 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells chr19:57906938..57906939 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - RMVar_hsa_circ_9920,RMVar_hsa_circ_196465,RMVar_hsa_circ_94305 52636 RMVar_ID_52636 Human_SNP_ID_832368727 A-to-I Human chr19 + 57873383 57873383 57873383 TGCTGGTGTAGAATGAGGTTACCCTTGTGACTAAAACATTTCCCACATTCCCCACACTTAAAAGG TGCTGGTGTAGAATGAGGTTACCCTTGTGACTGAAACATTTCCCACATTCCCCACACTTAAAAGG A G - - Other Unknown GSE100210 HepG2 cell line chr19:57873383..57873384 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_2571426 52637 RMVar_ID_52637 Human_SNP_ID_832372424 A-to-I Human chr19 + 38149300 38149300 38149300 GCGTGTGCCTGTCTTCCCTTGGGAGGCTGAGGAAAGAGAATATCGCTTGAACCCTGGAAGTGGAA GCGTGTGCCTGTCTTCCCTTGGGAGGCTGAGGCAAGAGAATATCGCTTGAACCCTGGAAGTGGAA A C SIPA1L3 Ensembl:ENSG00000105738 Protein coding intron GSE38233 cultured B-cells chr19:38149300..38149301 24183664 RNA-Seq:(High) rs8109695 Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_89034,RMVar_hsa_circ_194517,RMVar_hsa_circ_100903,RMVar_hsa_circ_194519,RMVar_hsa_circ_78151,RMVar_hsa_circ_105140,RMVar_hsa_circ_194533,RMVar_hsa_circ_39807,RMVar_hsa_circ_194526,RMVar_hsa_circ_194527,RMVar_hsa_circ_5608,RMVar_hsa_circ_30752,RMVar_hsa_circ_98955,RMVar_hsa_circ_104164,RMVar_hsa_circ_194531,RMVar_hsa_circ_120894,RMVar_hsa_circ_87100,RMVar_hsa_circ_194534,RMVar_hsa_circ_112006,RMVar_hsa_circ_122128,RMVar_hsa_circ_17616,RMVar_hsa_circ_311657,RMVar_hsa_circ_194532,RMVar_hsa_circ_194538,RMVar_hsa_circ_333358,RMVar_hsa_circ_353707,RMVar_hsa_circ_362881,RMVar_hsa_circ_194541,RMVar_hsa_circ_194542,RMVar_hsa_circ_194540,RMVar_hsa_circ_122454,RMVar_hsa_circ_87871,RMVar_hsa_circ_106617,RMVar_hsa_circ_194544,RMVar_hsa_circ_194546,RMVar_hsa_circ_194545,RMVar_hsa_circ_194543 52638 RMVar_ID_52638 Human_SNP_ID_832394984 A-to-I Human chr19 - 46736225 46736225 46736225 TTGCCCAGGCTGCAGTGCAGTGGCACGATCTCAGCTCACTGCAACCTCTGCCTCCATCCACCTCA TTGCCCAGGCTGCAGTGCAGTGGCACGATCTCGGCTCACTGCAACCTCTGCCTCCATCCACCTCA T C STRN4 Ensembl:ENSG00000090372 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr19:46736224..46736225 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_13480229 Human_Splice_Rec_2022926 RMVar_hsa_circ_82942,RMVar_hsa_circ_195494,RMVar_hsa_circ_120653,RMVar_hsa_circ_195499,RMVar_hsa_circ_5612,RMVar_hsa_circ_358829,RMVar_hsa_circ_359601 52639 RMVar_ID_52639 Human_SNP_ID_832400050 A-to-I Human chr19 + 53004758 53004758 53004758 GTTGCTGATGCCTCAAAAAGTGTGCAGGTCTCAATTCTGAAGACAGAGTTCCTACCACTCCTGAG GTTGCTGATGCCTCAAAAAGTGTGCAGGTCTCGATTCTGAAGACAGAGTTCCTACCACTCCTGAG A G AC010328.2 Ensembl:ENSG00000268282 Pseudogene exon GSE100210 HepG2 cell line chr19:53004757..53004758 29129909 RNA-Seq:(High) rs879211707 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_5586599 Human_miRNA_ID_1909167 52640 RMVar_ID_52640 Human_SNP_ID_832417431 A-to-I Human chr19 + 1946431 1946431 1946431 CTCCTGCCTCAGCTTCCCGAGTAGCTGGGACTACAGGCGACCGCCACCACGCCTGGCTAGTTTTT CTCCTGCCTCAGCTTCCCGAGTAGCTGGGACTGCAGGCGACCGCCACCACGCCTGGCTAGTTTTT A G CSNK1G2 Ensembl:ENSG00000133275 Protein coding intron GSE100210 HepG2 cell line chr19:1946430..1946431 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 2 ovary 52641 RMVar_ID_52641 Human_SNP_ID_832423132 A-to-I Human chr19 + 19352110 19352110 19352110 ACCTCAGGTGATCTGCCTACTTCAGCCTCCCAAAGTGCTGGGATTACAGACGTGAGCCACTGGGT ACCTCAGGTGATCTGCCTACTTCAGCCTCCCATAGTGCTGGGATTACAGACGTGAGCCACTGGGT A T MAU2 Ensembl:ENSG00000129933 Protein coding intron GSE100210 HepG2 cell line chr19:19352110..19352111 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 UTCA 1 - RMVar_hsa_circ_4883,RMVar_hsa_circ_193629,RMVar_hsa_circ_371806,RMVar_hsa_circ_25620 52642 RMVar_ID_52642 Human_SNP_ID_832438046 A-to-I Human chr19 + 11834196 11834196 11834196 TCACCCAGGCTGGAGTGCAGTGGCATGATCTCAGGTCACTGCAACCTCTGCCTCCAGGGTTCAAG TCACCCAGGCTGGAGTGCAGTGGCATGATCTCGGGTCACTGCAACCTCTGCCTCCAGGGTTCAAG A G ZNF440 Ensembl:ENSG00000171295 Protein coding 3'UTR GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells chr19:11834195..11834196 23474544,24183664 RNA-Seq:(High) - Functional Loss SNV TCGA 33..33 33 UCEC 1 - RMVar_hsa_circ_79330,RMVar_hsa_circ_192644 52643 RMVar_ID_52643 Human_SNP_ID_832438246 A-to-I Human chr19 + 18030699 18030699 18030699 CAAGAATGCATCTTGTCTTGTTCTTGCAGCCCAGCATGCCAGTGCTTCCTCCATGAATTTGAAAG CAAGAATGCATCTTGTCTTGTTCTTGCAGCCCGGCATGCCAGTGCTTCCTCCATGAATTTGAAAG A G AC020904.2 Ensembl:ENSG00000273654 Pseudogene exon GSE38233 cultured B-cells chr19:18030698..18030699 24183664 RNA-Seq:(High) rs1241667450 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_Splice_Rec_1979078 Human_miRNA_ID_1868488,Human_miRNA_ID_1909089 52644 RMVar_ID_52644 Human_SNP_ID_832447049 A-to-I Human chr19 - 18315426 18315426 18315426 GAACTTCAGGTTGGGCATGGTGGCTCAGGCCTATAATTCCAGCACTTTGGGAGGCTGAGGCTAGA GAACTTCAGGTTGGGCATGGTGGCTCAGGCCTGTAATTCCAGCACTTTGGGAGGCTGAGGCTAGA T C LSM4 Ensembl:ENSG00000130520 Protein coding intron GSE38233 cultured B-cells chr19:18315425..18315426 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 3 liver 52645 RMVar_ID_52645 Human_SNP_ID_832452557 A-to-I Human chr19 + 40003311 40003311 40003311 TGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGTGCCCAGCTTAAAATT TGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTGCAGGCGTGAGCCACCGTGCCCAGCTTAAAATT A G ZNF546 Ensembl:ENSG00000187187 Protein coding intron GSE100210 HepG2 cell line chr19:40003310..40003311 29129909 RNA-Seq:(High) rs1190651715 Functional Loss SNV ICGC 33..33 33 PRAD 1 - 52646 RMVar_ID_52646 Human_SNP_ID_832456210 A-to-I Human chr19 - 12894213 12894213 12894213 ACAGCAACTTCTGTGGCCATACGCTTCTCATAAAAAGTACAAAGTTTGCGTTCATCGTCCACTTC ACAGCAACTTCTGTGGCCATACGCTTCTCATAGAAAGTACAAAGTTTGCGTTCATCGTCCACTTC T C - - Other Unknown GSE100210 HepG2 cell line chr19:12894212..12894213 29129909 RNA-Seq:(High) rs879021899 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 haematopoietic and lymphoid tissue 52647 RMVar_ID_52647 Human_SNP_ID_832457391 A-to-I Human chr19 + 18365422 18365422 18365422 TGGAGTACAGTAGTGTGATCATGGATCACTGCAGCCTCTACCTCCTGGGCTCAAGTGATCCTCCC TGGAGTACAGTAGTGTGATCATGGATCACTGCGGCCTCTACCTCCTGGGCTCAAGTGATCCTCCC A G PGPEP1 Ensembl:ENSG00000130517 Protein coding 3'UTR GSE38233 cultured B-cells chr19:18365421..18365422 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_108567,RMVar_hsa_circ_193465 52648 RMVar_ID_52648 Human_SNP_ID_832464663 A-to-I Human chr19 - 52810652 52810652 52810652 CGCTCTAGCCCGGCCCCTGTAGACGCGACCCCAGAGCCTGCTGTTAAAACCACTGTAGAATGGAG CGCTCTAGCCCGGCCCCTGTAGACGCGACCCCGGAGCCTGCTGTTAAAACCACTGTAGAATGGAG T C ZNF28 Ensembl:ENSG00000198538 Protein coding intron GSE100210 HepG2 cell line chr19:52810651..52810652 29129909 RNA-Seq:(High) rs878955808 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue RMVar_hsa_circ_60331 52649 RMVar_ID_52649 Human_SNP_ID_832485323 A-to-I Human chr19 - 38869067 38869067 38869067 TTCACACCCCTCCGTTCATGCCTGTAATCCCAACATTTTGGGAGGCCAAGGTGGGAGGATTGCTT TTCACACCCCTCCGTTCATGCCTGTAATCCCAGCATTTTGGGAGGCCAAGGTGGGAGGATTGCTT T C RINL Ensembl:ENSG00000187994 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line chr19:38869066..38869067 31158229 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 ESCA,large_intestine adenocarcinoma,cervix squamous_cell_carcinoma 5 uterus,large intestine Human_Splice_Rec_2004172,Human_Splice_Rec_2004196,Human_Splice_Rec_2004212 52650 RMVar_ID_52650 Human_SNP_ID_832491249 A-to-I Human chr19 + 40857449 40857449 40857449 TAGACACGGGGTTTTACTATATTGGCCAGGCTAGTCTTGAACTCCTGACCTCAACTGATATGCCG TAGACACGGGGTTTTACTATATTGGCCAGGCTGGTCTTGAACTCCTGACCTCAACTGATATGCCG A G AC008537.1 Ensembl:ENSG00000268797 Protein coding intron GSE100210 HepG2 cell line chr19:40857448..40857449 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 52651 RMVar_ID_52651 Human_SNP_ID_832501384 A-to-I Human chr19 + 57873217 57873217 57873217 CTGATGTGCAATGAGTTGGTACTTGTTTCTAAAAAATTTCTGACAAGCTTCACAAGCATATGGCT CTGATGTGCAATGAGTTGGTACTTGTTTCTAACAAATTTCTGACAAGCTTCACAAGCATATGGCT A C - - Other Unknown GSE100210 HepG2 cell line chr19:57873217..57873218 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 pancreas ductal_carcinoma 7 pancreas Human_RBP_ID_2571424,Human_RBP_ID_18740885,Human_RBP_ID_27684108 52652 RMVar_ID_52652 Human_SNP_ID_832516011 A-to-I Human chr19 - 41981294 41981294 41981294 GACGCTGAGGAGTAAAGATCTTCCTGCAGGCCAGGCGCGGTGGCTCACACCTTTAACACCAGAAC GACGCTGAGGAGTAAAGATCTTCCTGCAGGCCTGGCGCGGTGGCTCACACCTTTAACACCAGAAC T A AC010616.1,ATP1A3 Ensembl:ENSG00000285505,Ensembl:ENSG00000105409 Protein coding,Protein coding intron,intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank chr19:41981293..41981294 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - RMVar_hsa_circ_195053,RMVar_hsa_circ_85073,RMVar_hsa_circ_48193 52653 RMVar_ID_52653 Human_SNP_ID_832524822 A-to-I Human chr19 + 35770107 35770107 35770107 TTGTATTTTTAGTAGAGACGGGGTTTCACCATATTGGCCAGGCTGGTCTCAAACTCATGACCTCG TTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTCATGACCTCG A G PROSER3 Ensembl:ENSG00000167595 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line chr19:35770106..35770107 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs911471640 Functional Loss SNV ICGC 33..33 33 ESCA 1 - 52654 RMVar_ID_52654 Human_SNP_ID_832527955 A-to-I Human chr19 - 1203345 1203345 1203345 TCTCCTTTGCAGACGTGGTCTTCCATCTCTCCAAACACTTCTTGGAGAATTCCACGAAATTGACA TCTCCTTTGCAGACGTGGTCTTCCATCTCTCCGAACACTTCTTGGAGAATTCCACGAAATTGACA T C - - Other Unknown GSE100210 HepG2 cell line chr19:1203344..1203345 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 1 - 52655 RMVar_ID_52655 Human_SNP_ID_832530870 A-to-I Human chr19 - 51366329 51366329 51366329 TGCGGGCTGACCCTGTAAGTGGCTGCGGCGGGAAGATGGCGGAGCTGCGCGTGCTCGTAGCTGTC TGCGGGCTGACCCTGTAAGTGGCTGCGGCGGGGAGATGGCGGAGCTGCGCGTGCTCGTAGCTGTC T C ETFB,AC008750.8 Ensembl:ENSG00000105379,Ensembl:ENSG00000269403 Protein coding,Protein coding 5'UTR,intron GSE100210 HepG2 cell line chr19:51366328..51366329 29129909 RNA-Seq:(High) rs776277833 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_241372,Human_RBP_ID_526004,Human_RBP_ID_4558709,Human_RBP_ID_5320552,Human_RBP_ID_5421792,Human_RBP_ID_9329168,Human_RBP_ID_9381345,Human_RBP_ID_17935082,Human_RBP_ID_18421674,Human_RBP_ID_22448991 Human_Splice_Rec_2037911,Human_Splice_Rec_2037921,Human_Splice_Rec_2037929 52656 RMVar_ID_52656 Human_SNP_ID_832535364 A-to-I Human chr19 + 47268959 47268959 47268959 TAATAATAATAATAATAATGTGTGTCTGGGCCAGGCGTGGTGGCTCATGCTTGTAATCCCCACAA TAATAATAATAATAATAATGTGTGTCTGGGCCGGGCGTGGTGGCTCATGCTTGTAATCCCCACAA A G CCDC9 Ensembl:ENSG00000105321 Protein coding intron GSE100210 HepG2 cell line chr19:47268958..47268959 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 OV 1 - RMVar_hsa_circ_76127,RMVar_hsa_circ_195574 52657 RMVar_ID_52657 Human_SNP_ID_832539122 A-to-I Human chr19 - 10167298 10167298 10167298 CCAGCTACTTGGGAGACTGAGGCAGGAGAATCACTTGAACCCGGGAGGCGGTGGTTGCAGTGAGC CCAGCTACTTGGGAGACTGAGGCAGGAGAATCGCTTGAACCCGGGAGGCGGTGGTTGCAGTGAGC T C DNMT1 Ensembl:ENSG00000130816 Protein coding intron GSE38233 cultured B-cells chr19:10167297..10167298 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 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_267045,RMVar_hsa_circ_192316,RMVar_hsa_circ_284314,RMVar_hsa_circ_327144,RMVar_hsa_circ_363399,RMVar_hsa_circ_60933 52658 RMVar_ID_52658 Human_SNP_ID_832548134 A-to-I Human chr19 + 785098 785098 785098 CAACGTGGAGAAACCCCGTCTCTACTAAAAATACAAAATTAGCCAGGCGTGGTGGCGCAGCTACT CAACGTGGAGAAACCCCGTCTCTACTAAAAATGCAAAATTAGCCAGGCGTGGTGGCGCAGCTACT A G LINC01836 Ensembl:ENSG00000267530 lincRNA exon GSE100210 HepG2 cell line chr19:785097..785098 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LMS 1 - Human_Splice_Rec_1928939 52659 RMVar_ID_52659 Human_SNP_ID_832577414 A-to-I Human chr19 - 36320497 36320497 36320497 CCTTGGCCTCTCAAAGTGCTGGGATTACAGGCATGAGCCACCGCACCTGGCTGTTTTTTCATTTC CCTTGGCCTCTCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCACCTGGCTGTTTTTTCATTTC T C LINC00665 Ensembl:ENSG00000232677 lincRNA intron GSE123020:GSM3490829,GSM3490830,GSM3490831 esophageal squamous carcinoma cells,EC109 cell line chr19:36320496..36320497 32596459 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - 52660 RMVar_ID_52660 Human_SNP_ID_832587238 A-to-I Human chr19 + 39427288 39427288 39427288 TGACCTCGTGATCCTCCCGCCTCGGCCTCCCAAAGTGCTGGCATTACAGGCGTGAGCCATCATTC TGACCTCGTGATCCTCCCGCCTCGGCCTCCCATAGTGCTGGCATTACAGGCGTGAGCCATCATTC A T PLEKHG2 Ensembl:ENSG00000090924 Protein coding 3'UTR GSE38233 cultured B-cells chr19:39427288..39427289 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 2 ovary RMVar_hsa_circ_88824,RMVar_hsa_circ_194740 52661 RMVar_ID_52661 Human_SNP_ID_832588097 A-to-I Human chr19 - 13331279 13331279 13331279 TGAGCCGAGATCACACCACTGCACTCCAGCCTAGGCGACAGAGCAAGACTCTGTCTCAAAAAAAA TGAGCCGAGATCACACCACTGCACTCCAGCCTGGGCGACAGAGCAAGACTCTGTCTCAAAAAAAA T C CACNA1A Ensembl:ENSG00000141837 Protein coding intron GSE107867 ASD brains,cerebellum chr19:13331278..13331279 30559470 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 15 prostate RMVar_hsa_circ_100582,RMVar_hsa_circ_192883,RMVar_hsa_circ_106634,RMVar_hsa_circ_192886,RMVar_hsa_circ_6638,RMVar_hsa_circ_12455,RMVar_hsa_circ_89082,RMVar_hsa_circ_192896,RMVar_hsa_circ_332679,RMVar_hsa_circ_339181,RMVar_hsa_circ_192903,RMVar_hsa_circ_301557,RMVar_hsa_circ_192902 52662 RMVar_ID_52662 Human_SNP_ID_832590952 A-to-I Human chr19 + 35575675 35575675 35575675 CAGCAGGACGGTGGCCATGGAAGTCAGAATCCACTAAGGAGTGTGTAACAACTCACCTGCCGAAT CAGCAGGACGGTGGCCATGGAAGTCAGAATCCGCTAAGGAGTGTGTAACAACTCACCTGCCGAAT A G AD000090.1 Ensembl:ENSG00000283907 lincRNA exon GSE100210 HepG2 cell line chr19:35575674..35575675 29129909 RNA-Seq:(High) rs79755095 Functional Loss SNV ICGC 33..33 33 LMS 1 - 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_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 52663 RMVar_ID_52663 Human_SNP_ID_832599202 A-to-I Human chr19 - 52896256 52896256 52896256 CGAAATCTCGTGTCGAATAAAATACAGAAATTAGCCAGGTGTGATGTCGGGCGCCTGTAATCCCA CGAAATCTCGTGTCGAATAAAATACAGAAATTTGCCAGGTGTGATGTCGGGCGCCTGTAATCCCA T A ZNF320 Ensembl:ENSG00000182986 Protein coding intron GSE38233 cultured B-cells chr19:52896255..52896256 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_196178,RMVar_hsa_circ_100352 52664 RMVar_ID_52664 Human_SNP_ID_832618465 A-to-I Human chr19 - 15393843 15393843 15393843 GCTGGAGTGCAATGGCGCGATCTCGGCTCACCACAACCTCTGCCTCCCGGGTCCAAGCAATTCTC GCTGGAGTGCAATGGCGCGATCTCGGCTCACCGCAACCTCTGCCTCCCGGGTCCAAGCAATTCTC T C AKAP8L Ensembl:ENSG00000011243 Protein coding intron GSE100210 HepG2 cell line chr19:15393842..15393843 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 OV 1 - Human_RBP_ID_25387054 RMVar_hsa_circ_26700,RMVar_hsa_circ_118166,RMVar_hsa_circ_265663,RMVar_hsa_circ_51331,RMVar_hsa_circ_193137 52665 RMVar_ID_52665 Human_SNP_ID_832645752 A-to-I Human chr19 - 36319974 36319974 36319974 AAACCCCCTCTCTACTAAAAATACAAAAAATTAGCTGGGCGTGGTGGCAGGCGCCTGTAGTCCCA AAACCCCCTCTCTACTAAAAATACAAAAAATTGGCTGGGCGTGGTGGCAGGCGCCTGTAGTCCCA T C LINC00665 Ensembl:ENSG00000232677 lincRNA intron GSE47997 K562 cells&HepG2 cells chr19:36319973..36319974 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 52666 RMVar_ID_52666 Human_SNP_ID_832651534 A-to-I Human chr19 - 2934284 2934284 2934284 AAGGAGTGTGGGAAAGCCTTCAGCTGTCCCTCATACTTTCGAGAACATGTCAGAACACACACTGG AAGGAGTGTGGGAAAGCCTTCAGCTGTCCCTCGTACTTTCGAGAACATGTCAGAACACACACTGG T C ZNF77 Ensembl:ENSG00000175691 Protein coding CDS GSE38233 cultured B-cells chr19:2934283..2934284 24183664 RNA-Seq:(High) rs3746073 Functional Loss SNV ICGC 33..33 33 COCA 2 - GWAS_ID_2283 52667 RMVar_ID_52667 Human_SNP_ID_832652453 A-to-I Human chr19 - 12894205 12894205 12894205 TTCTGTGGCCATACGCTTCTCATAAAAAGTACAAAGTTTGCGTTCATCGTCCACTTCAATGAGTT TTCTGTGGCCATACGCTTCTCATAAAAAGTACGAAGTTTGCGTTCATCGTCCACTTCAATGAGTT T C - - Other Unknown GSE100210 HepG2 cell line chr19:12894204..12894205 29129909 RNA-Seq:(High) rs879115966 Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 3 breast 52668 RMVar_ID_52668 Human_SNP_ID_832656004 A-to-I Human chr19 - 38868589 38868589 38868589 TCTGTCTGTTGCCCAGGCTGGAGTGTAGTGGCATGATCTCGGCTCACTGCAGCCTTAACCTCCTG TCTGTCTGTTGCCCAGGCTGGAGTGTAGTGGCGTGATCTCGGCTCACTGCAGCCTTAACCTCCTG T C RINL Ensembl:ENSG00000187994 Protein coding 3'UTR GSE38233 cultured B-cells chr19:38868588..38868589 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_26472470 52669 RMVar_ID_52669 Human_SNP_ID_832661000 A-to-I Human chr19 - 49866001 49866001 49866001 CTCAAAAAAAGAAAAGAAAAAATATGGCTGGGAGAGAAGGGGATGTGTCCAGTAAAGAAAGAAGT CTCAAAAAAAGAAAAGAAAAAATATGGCTGGGGGAGAAGGGGATGTGTCCAGTAAAGAAAGAAGT T C PNKP Ensembl:ENSG00000039650 Protein coding intron GSE100210 HepG2 cell line chr19:49866000..49866001 29129909 RNA-Seq:(High) rs994801798 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_13497813 RMVar_hsa_circ_113881,RMVar_hsa_circ_195958 52670 RMVar_ID_52670 Human_SNP_ID_832665440 A-to-I Human chr19 - 12894245 12894245 12894245 CGTAACCCTTCCATTCTTCACCCAGAGCGTCAACAGCAACTTCTGTGGCCATACGCTTCTCATAA CGTAACCCTTCCATTCTTCACCCAGAGCGTCAGCAGCAACTTCTGTGGCCATACGCTTCTCATAA T C - - Other Unknown GSE100210 HepG2 cell line chr19:12894244..12894245 29129909 RNA-Seq:(High) rs878946393 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 haematopoietic and lymphoid tissue 52671 RMVar_ID_52671 Human_SNP_ID_832667468 A-to-I Human chr19 + 47180652 47180652 47180652 TGAGACCAGCCTGGGCAACAAAACGAGACCCCATCTCTACAAAAAATAAAAAAGTTAGCCAGATA TGAGACCAGCCTGGGCAACAAAACGAGACCCCGTCTCTACAAAAAATAAAAAAGTTAGCCAGATA A G SAE1 Ensembl:ENSG00000142230 Protein coding intron GSE38233 cultured B-cells chr19:47180651..47180652 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 5 ovary RMVar_hsa_circ_44245,RMVar_hsa_circ_195562,RMVar_hsa_circ_347680,RMVar_hsa_circ_118551,RMVar_hsa_circ_296637 52672 RMVar_ID_52672 Human_SNP_ID_832687196 A-to-I Human chr19 - 4820974 4820974 4820974 TTGACCAGGCTGATCTTGAACTCATGACCTCAAATGATCTGTCCGCCTTAGCTTCCCAAAGTGCT TTGACCAGGCTGATCTTGAACTCATGACCTCATATGATCTGTCCGCCTTAGCTTCCCAAAGTGCT T A TICAM1 Ensembl:ENSG00000127666 Protein coding intron GSE100210 HepG2 cell line chr19:4820973..4820974 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 52673 RMVar_ID_52673 Human_SNP_ID_832715373 A-to-I Human chr19 + 21119176 21119176 21119176 CCTATAATCCCAGCACTTTGGTAGGCCAAGGCAGGTGGATCATGAGGTCAGGAGTTTGAGACCAG CCTATAATCCCAGCACTTTGGTAGGCCAAGGCGGGTGGATCATGAGGTCAGGAGTTTGAGACCAG A G ZNF714 Ensembl:ENSG00000160352 Protein coding intron GSE100210;GSE99789 HepG2 cell line;esophageal squamous carcinoma cells,EC109 chr19:21119175..21119176 29129909,29796672 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue Human_RBP_ID_13408617 52674 RMVar_ID_52674 Human_SNP_ID_832726121 A-to-I Human chr19 + 43998032 43998032 43998032 GTAAATCATCACTTCAGCTCCTGATTGGTCCCAGGCCAAGCTGAATAGCCCTTAGGAATAATCAC GTAAATCATCACTTCAGCTCCTGATTGGTCCCGGGCCAAGCTGAATAGCCCTTAGGAATAATCAC A G ZNF155 Ensembl:ENSG00000204920 Protein coding 3'UTR GSE38233 cultured B-cells chr19:43998031..43998032 24183664 RNA-Seq:(High) rs377503 Functional Loss SNV ICGC 33..33 33 ESCA 1 - 52675 RMVar_ID_52675 Human_SNP_ID_832730518 A-to-I Human chr19 + 53541886 53541886 53541886 TTGAAAAAGATTAGCCAGGCATGGTGATGCATACCTATAGTTTCAGCTACTCAGAAGGCTGCTGT TTGAAAAAGATTAGCCAGGCATGGTGATGCATGCCTATAGTTTCAGCTACTCAGAAGGCTGCTGT A G ZNF331 Ensembl:ENSG00000130844 Protein coding intron GSE100210 HepG2 cell line chr19:53541885..53541886 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_9624,RMVar_hsa_circ_17810,RMVar_hsa_circ_336166,RMVar_hsa_circ_320463,RMVar_hsa_circ_347035,RMVar_hsa_circ_196205 52676 RMVar_ID_52676 Human_SNP_ID_832734864 A-to-I Human chr19 + 19332224 19332224 19332224 GCCCTGTTGCCCAGGCTGGAGTGCAACAGCACAATCATAGCTCACTGCAGCCCCAAACTCCTGGG GCCCTGTTGCCCAGGCTGGAGTGCAACAGCACGATCATAGCTCACTGCAGCCCCAAACTCCTGGG A G MAU2 Ensembl:ENSG00000129933 Protein coding intron GSE38233 cultured B-cells chr19:19332223..19332224 24183664 RNA-Seq:(High) rs1557723 Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_193623,RMVar_hsa_circ_111927 52677 RMVar_ID_52677 Human_SNP_ID_832748783 A-to-I Human chr19 - 36516851 36516839 36516851 CAAGTCGGCCGGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGCAG CAAGTCGGCCGGGCGCAGTGGCTCACGCCTGT____________TTGGGAGGCCAAGGCGGGCAG AAGTGCTGGGATT A ZNF260 Ensembl:ENSG00000254004 Protein coding intron GSE100210 HepG2 cell line chr19:36516850..36516851 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 33..44 33 MALY 1 - RMVar_hsa_circ_194417,RMVar_hsa_circ_121682 52678 RMVar_ID_52678 Human_SNP_ID_832755253 A-to-I Human chr19 + 57869458 57869458 57869458 AAAATGGAAAGTACTCTACTGTACAGCAAAGTAAATCATTGGTTGTCTGGAGAACAGAAAGAAAG AAAATGGAAAGTACTCTACTGTACAGCAAAGTTAATCATTGGTTGTCTGGAGAACAGAAAGAAAG A T - - Other Unknown GSE100210 HepG2 cell line chr19:57869457..57869458 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - Human_RBP_ID_1573207,Human_RBP_ID_8495395,Human_RBP_ID_22503874 52679 RMVar_ID_52679 Human_SNP_ID_832765531 A-to-I Human chr19 - 41338407 41338407 41338407 ACGGCAACCTCCACCTCCCGGGGGTTCAAGCAATTCTCCTGCTTCAGCCTCCTGAGTAGTTGGGA ACGGCAACCTCCACCTCCCGGGGGTTCAAGCATTTCTCCTGCTTCAGCCTCCTGAGTAGTTGGGA T A TGFB1 Ensembl:ENSG00000105329 Protein coding intron GSE38233 cultured B-cells chr19:41338406..41338407 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_195011,RMVar_hsa_circ_105511,RMVar_hsa_circ_195012,RMVar_hsa_circ_374029 52680 RMVar_ID_52680 Human_SNP_ID_832772200 A-to-I Human chr19 + 35575759 35575759 35575759 ATGGCACTGGAGCATCAGGCCCATACCCGGCCATCGCCAGCAGTCAATGGAATGTGAGTGCCTTA ATGGCACTGGAGCATCAGGCCCATACCCGGCCGTCGCCAGCAGTCAATGGAATGTGAGTGCCTTA A G AD000090.1 Ensembl:ENSG00000283907 lincRNA exon GSE100210 HepG2 cell line chr19:35575758..35575759 29129909 RNA-Seq:(High) rs79083609 Functional Loss SNV ICGC 33..33 33 LMS 1 - Human_RBP_ID_270008,Human_RBP_ID_1064019,Human_RBP_ID_5194225,Human_RBP_ID_8103461,Human_RBP_ID_26467463 52681 RMVar_ID_52681 Human_SNP_ID_832776688 A-to-I Human chr19 - 43491594 43491594 43491594 GGGAGGCTGAGGCAGGAGAATAGTTTGAACCCAGGAGATGGAGGTTTCGGTGAGCTAAGGTCGCA GGGAGGCTGAGGCAGGAGAATAGTTTGAACCCGGGAGATGGAGGTTTCGGTGAGCTAAGGTCGCA T C PHLDB3 Ensembl:ENSG00000176531 Protein coding intron GSE100210 HepG2 cell line chr19:43491593..43491594 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 2 pancreas 52682 RMVar_ID_52682 Human_SNP_ID_832783480 A-to-I Human chr19 + 37792613 37792613 37792613 TATCCATCTCAGATACCAGCAACTCCCCCATCATATGAATCTGTAGATGACATTAATGCTGATAA TATCCATCTCAGATACCAGCAACTCCCCCATCGTATGAATCTGTAGATGACATTAATGCTGATAA A G AC016582.2 Ensembl:ENSG00000267422 Pseudogene intron GSE100210 HepG2 cell line chr19:37792612..37792613 29129909 RNA-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 52683 RMVar_ID_52683 Human_SNP_ID_832793747 A-to-I Human chr19 - 43585064 43585064 43585064 TTTCATGAGCCCAGGAGATCGAGACTAGCCTGAGCAACATGGCAAGACCCCCATCTCTACAAAAA TTTCATGAGCCCAGGAGATCGAGACTAGCCTGGGCAACATGGCAAGACCCCCATCTCTACAAAAA T C IRGQ,L34079.1 Ensembl:ENSG00000167378,Ensembl:ENSG00000268361 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line chr19:43585063..43585064 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 3 pancreas 52684 RMVar_ID_52684 Human_SNP_ID_832797829 A-to-I Human chr19 - 52618197 52618195 52618198 ATCCCAGGTACTAGAAAGGCTAAGGTAAGATTATCACCTGAACCTGGGAGGCAATGGTTGCAGTG ATCCCAGGTACTAGAAAGGCTAAGGTAAGAT___CACCTGAACCTGGGAGGCAATGGTTGCAGTG GATA G ZNF83 Ensembl:ENSG00000167766 Protein coding intron GSE107867 ASD brains,cerebellum chr19:52618196..52618197 30559470 RNA-Seq:(High) - Functional Loss DEL ICGC 32..34 33 ESCA 1 - RMVar_hsa_circ_96700,RMVar_hsa_circ_196164,RMVar_hsa_circ_196163,RMVar_hsa_circ_196165,RMVar_hsa_circ_349281 52685 RMVar_ID_52685 Human_SNP_ID_832799731 A-to-I Human chr19 + 45694673 45694673 45694673 TTTGTATTTTTAGTGAGACGGGGTTTCACCATATTGGCCAGGCTGGTCTCAAACTCCTGACCTTA TTTGTATTTTTAGTGAGACGGGGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTCCTGACCTTA A G QPCTL Ensembl:ENSG00000011478 Protein coding intron GSE38233 cultured B-cells chr19:45694672..45694673 24183664 RNA-Seq:(High) rs1318106080 Functional Loss SNV ICGC 33..33 33 PBCA 1 - 52686 RMVar_ID_52686 Human_SNP_ID_832803139 A-to-I Human chr19 + 53214282 53214282 53214282 TTTTTTGTATTTTTTAGTAGATACGGGGTTTCACCATATCGGCCAGGCTGGTCTCGAACTCCTGA TTTTTTGTATTTTTTAGTAGATACGGGGTTTCTCCATATCGGCCAGGCTGGTCTCGAACTCCTGA A T AC092070.2 Ensembl:ENSG00000269001 Pseudogene exon GSE38233 cultured B-cells chr19:53214281..53214282 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 52687 RMVar_ID_52687 Human_SNP_ID_832805516 A-to-I Human chr19 + 57862048 57862048 57862048 CACCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTCAGCCACTGTACCTGGCTGAATACT CACCTGCCTCGGCCTCCCAAAGTGCTGGGATTGCAGGTGTCAGCCACTGTACCTGGCTGAATACT A G ZNF587 Ensembl:ENSG00000198466 Protein coding 3'UTR GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line chr19:57862047..57862048 29129909,31158229 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_1892899,Human_RBP_ID_13523590 RMVar_hsa_circ_196462,RMVar_hsa_circ_87749 52688 RMVar_ID_52688 Human_SNP_ID_832807842 A-to-I Human chr19 - 1203324 1203324 1203324 TCCATCTCTCCAAACACTTCTTGGAGAATTCCACGAAATTGACAGAAGAGTCCGGGTGTTTCTTC TCCATCTCTCCAAACACTTCTTGGAGAATTCCGCGAAATTGACAGAAGAGTCCGGGTGTTTCTTC T C - - Other Unknown GSE100210 HepG2 cell line chr19:1203323..1203324 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 1 - 52689 RMVar_ID_52689 Human_SNP_ID_832816383 A-to-I Human chr19 - 19177462 19177462 19177462 ACTACCCCCAGCTAATTTTTTGTATTTTTTGTAGAGACGGGGTTTCACCATGTTGGCTAGGCTGG ACTACCCCCAGCTAATTTTTTGTATTTTTTGTGGAGACGGGGTTTCACCATGTTGGCTAGGCTGG T C BORCS8,MEF2B,BORCS8-MEF2B Ensembl:ENSG00000254901,Ensembl:ENSG00000213999,Ensembl:ENSG00000064489 Protein coding,Protein coding,Protein coding 3'UTR,intron,intron GSE100210 HepG2 cell line chr19:19177461..19177462 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 bile_duct adenocarcinoma,biliary_tract adenocarcinoma 4 biliary tract,gallbladder Human_Splice_Rec_1982638 RMVar_hsa_circ_104466,RMVar_hsa_circ_106768,RMVar_hsa_circ_193593,RMVar_hsa_circ_108817,RMVar_hsa_circ_193595,RMVar_hsa_circ_193597,RMVar_hsa_circ_99317,RMVar_hsa_circ_193596 52690 RMVar_ID_52690 Human_SNP_ID_832832720 A-to-I Human chr19 + 12239816 12239816 12239816 AGCTGGTCTTGGAACTCCTGACCTCGTGCTCCACCCGCCTTGGCTTCCCAAAGTGCTGGGATTAC AGCTGGTCTTGGAACTCCTGACCTCGTGCTCCCCCCGCCTTGGCTTCCCAAAGTGCTGGGATTAC A C LOC100289333 RNACentral:URS00008BE083 lincRNA intron GSE100210 HepG2 cell line chr19:12239815..12239816 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 52691 RMVar_ID_52691 Human_SNP_ID_832841220 A-to-I Human chr19 - 45571348 45571348 45571348 GAGGCGGGGAGTTCAAGACCAACCTGAACAACATGGAGAAACCCCGTCTCTACTAAAAAAATACA GAGGCGGGGAGTTCAAGACCAACCTGAACAACGTGGAGAAACCCCGTCTCTACTAAAAAAATACA T C OPA3 Ensembl:ENSG00000125741 Protein coding intron GSE100210 HepG2 cell line chr19:45571347..45571348 29129909 RNA-Seq:(High) rs1332784452 Functional Loss SNV ICGC 33..33 33 PBCA 1 - 52692 RMVar_ID_52692 Human_SNP_ID_832844936 A-to-I Human chr19 - 57688042 57688042 57688042 GAGCTCTGGCTAAAGGATTTCCCACATTCACTACATTCATAAGGCCTTTCTCCAGTGTGAACTCT GAGCTCTGGCTAAAGGATTTCCCACATTCACTGCATTCATAAGGCCTTTCTCCAGTGTGAACTCT T C - - Other Unknown GSE107867 ASD brains,temporal_cortex chr19:57688041..57688042 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm,large_intestine adenocarcinoma,cervix squamous_cell_carcinoma 10 uterus,liver,large intestine 52693 RMVar_ID_52693 Human_SNP_ID_832852019 A-to-I Human chr19 + 12950837 12950837 12950837 CCTGTAATCCCAGCACTTTGGGAGGCTAAGGCAGGCAGACCACTTGGTCAGGAGTTTTAGACCAG CCTGTAATCCCAGCACTTTGGGAGGCTAAGGCGGGCAGACCACTTGGTCAGGAGTTTTAGACCAG A G RAD23A Ensembl:ENSG00000179262 Protein coding intron GSE38233 cultured B-cells chr19:12950836..12950837 24183664 RNA-Seq:(High) rs74181683 Functional Loss SNV ICGC,COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma,CLLE 4 haematopoietic and lymphoid tissue 52694 RMVar_ID_52694 Human_SNP_ID_832853473 A-to-I Human chr19 + 38151601 38151601 38151601 CAACCTCAGACAGGGAGAAGACCTTCTACCACAACCGGCTGTGATCCAAGGAGGACTGGACGTTA CAACCTCAGACAGGGAGAAGACCTTCTACCACGACCGGCTGTGATCCAAGGAGGACTGGACGTTA A G SIPA1L3 Ensembl:ENSG00000105738 Protein coding intron GSE38233 cultured B-cells chr19:38151600..38151601 24183664 RNA-Seq:(High) rs332845 Functional Loss SNV ICGC 33..33 33 LAML 1 - GWAS_ID_2625 RMVar_hsa_circ_89034,RMVar_hsa_circ_194517,RMVar_hsa_circ_100903,RMVar_hsa_circ_194519,RMVar_hsa_circ_78151,RMVar_hsa_circ_105140,RMVar_hsa_circ_194533,RMVar_hsa_circ_39807,RMVar_hsa_circ_194526,RMVar_hsa_circ_194527,RMVar_hsa_circ_5608,RMVar_hsa_circ_30752,RMVar_hsa_circ_98955,RMVar_hsa_circ_104164,RMVar_hsa_circ_194531,RMVar_hsa_circ_120894,RMVar_hsa_circ_87100,RMVar_hsa_circ_194534,RMVar_hsa_circ_112006,RMVar_hsa_circ_122128,RMVar_hsa_circ_17616,RMVar_hsa_circ_311657,RMVar_hsa_circ_194532,RMVar_hsa_circ_194538,RMVar_hsa_circ_333358,RMVar_hsa_circ_353707,RMVar_hsa_circ_362881,RMVar_hsa_circ_194541,RMVar_hsa_circ_194542,RMVar_hsa_circ_194540,RMVar_hsa_circ_122454,RMVar_hsa_circ_87871,RMVar_hsa_circ_106617,RMVar_hsa_circ_194544,RMVar_hsa_circ_194546,RMVar_hsa_circ_194545,RMVar_hsa_circ_194543 52695 RMVar_ID_52695 Human_SNP_ID_832863015 A-to-I Human chr19 + 14070563 14070563 14070563 TGATCCTCCATGACATTGTGAGAGCCAGAGAGAACATCCAGAAATCCCTGGCTGGAAGCTCAGGC TGATCCTCCATGACATTGTGAGAGCCAGAGAGCACATCCAGAAATCCCTGGCTGGAAGCTCAGGC A C EEF1DP1 Ensembl:ENSG00000228887 Pseudogene exon GSE100210 HepG2 cell line chr19:14070562..14070563 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_4504596,Human_RBP_ID_17387667,Human_RBP_ID_18532807 Human_miRNA_ID_1854302,Human_miRNA_ID_1910372 52696 RMVar_ID_52696 Human_SNP_ID_832876256 A-to-I Human chr19 + 12189973 12189970 12189974 TCTTTCTTTCTGAAATAGGGTCTCACTCTGTCACTCAGGCTGGAGTGCAGTGGCACGACTGTGGC TCTTTCTTTCTGAAATAGGGTCTCACTCTG____TCAGGCTGGAGTGCAGTGGCACGACTGTGGC GTCAC G - - Other Unknown GSE100210 HepG2 cell line chr19:12189972..12189973 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 31..34 33 BRCA 1 - 52697 RMVar_ID_52697 Human_SNP_ID_832892254 A-to-I Human chr19 + 2835217 2835217 2835217 GTGGGAGGCAGGGTGCGGTGGCTCATGCCTATAATCCTAACACTTTAGGAGGCCGAGGCGGGTGG GTGGGAGGCAGGGTGCGGTGGCTCATGCCTATGATCCTAACACTTTAGGAGGCCGAGGCGGGTGG A G ZNF554 Ensembl:ENSG00000172006 Protein coding 3'UTR GSE100210 HepG2 cell line chr19:2835217..2835218 29129909 RNA-Seq:(High) rs1009748930 Functional Loss SNV ICGC 33..33 33 PBCA 1 - 52698 RMVar_ID_52698 Human_SNP_ID_832916689 A-to-I Human chr19 - 10165189 10165189 10165189 ACGGTTCACTGTAGCCTCGACCTCCCAGGCTCAGGTGATCTTCCCGCCTCAGCCTCCCAAGTAGC ACGGTTCACTGTAGCCTCGACCTCCCAGGCTCTGGTGATCTTCCCGCCTCAGCCTCCCAAGTAGC T A DNMT1 Ensembl:ENSG00000130816 Protein coding intron GSE100210 HepG2 cell line chr19:10165188..10165189 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 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_192316,RMVar_hsa_circ_284314 52699 RMVar_ID_52699 Human_SNP_ID_832917136 A-to-I Human chr19 - 16641427 16641427 16641427 GAGTGTGGTGGTACAGGCCTGTAATCCCAGTTACTAGGGAGGCTGAGGCAGGAGAATCACTTGAA GAGTGTGGTGGTACAGGCCTGTAATCCCAGTTCCTAGGGAGGCTGAGGCAGGAGAATCACTTGAA T G SMIM7,AC008764.4 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells chr19:16641426..16641427 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - Human_Splice_Rec_1974254 RMVar_hsa_circ_349256 52700 RMVar_ID_52700 Human_SNP_ID_832929841 A-to-I Human chr19 - 14483442 14483442 14483442 TTTTATTTTATTTTATTTATAGACGGAGCCTTAGTCTGTCACCCAGGCTAGAGTGCAGTGGTGCG TTTTATTTTATTTTATTTATAGACGGAGCCTTCGTCTGTCACCCAGGCTAGAGTGCAGTGGTGCG T G GIPC1 Ensembl:ENSG00000123159 Protein coding intron GSE100210 HepG2 cell line chr19:14483441..14483442 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - RMVar_hsa_circ_80215,RMVar_hsa_circ_193026,RMVar_hsa_circ_88431,RMVar_hsa_circ_193028 52701 RMVar_ID_52701 Human_SNP_ID_832931151 A-to-I Human chr19 + 45031314 45031314 45031314 CCTGGCTAATTTTTTAATTTTCTTGTAGAGACAAGGTCTTGCTGTGTTGGCCAGTCTGGTCTTGA CCTGGCTAATTTTTTAATTTTCTTGTAGAGACGAGGTCTTGCTGTGTTGGCCAGTCTGGTCTTGA A G RELB Ensembl:ENSG00000104856 Protein coding intron GSE100210 HepG2 cell line chr19:45031314..45031315 29129909 RNA-Seq:(High) rs979104285 Functional Loss SNV ICGC 33..33 33 LAML 1 - RMVar_hsa_circ_34073,RMVar_hsa_circ_119053,RMVar_hsa_circ_40758,RMVar_hsa_circ_332495,RMVar_hsa_circ_361060,RMVar_hsa_circ_195273 52702 RMVar_ID_52702 Human_SNP_ID_832950297 A-to-I Human chr19 + 11087176 11087176 11087176 TAAACTTATCTTTATTTTTGAGACACAGTCTCACTCTGTCGCCCAGGCTGGAGTGCAGTGGTACA TAAACTTATCTTTATTTTTGAGACACAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCAGTGGTACA A G - - Other Unknown GSE100210 HepG2 cell line chr19:11087175..11087176 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 52703 RMVar_ID_52703 Human_SNP_ID_832974611 A-to-I Human chr19 - 3965571 3965571 3965571 CTACGTTGCCCAGGCTGGAGTACAGTGGCACAATCTCAGTTCACTGCAACCTCTGCCTCCCAGGT CTACGTTGCCCAGGCTGGAGTACAGTGGCACACTCTCAGTTCACTGCAACCTCTGCCTCCCAGGT T G DAPK3 Ensembl:ENSG00000167657 Protein coding intron GSE38233 cultured B-cells chr19:3965570..3965571 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_191422,RMVar_hsa_circ_77341 52704 RMVar_ID_52704 Human_SNP_ID_832995386 A-to-I Human chr19 - 16563708 16563708 16563708 AGGAGACCGAGGTAGGTGGATCCCTTGAGGCCAGGAGTTCGAAACCAGCCTGGCCAACGTGGGGA AGGAGACCGAGGTAGGTGGATCCCTTGAGGCCTGGAGTTCGAAACCAGCCTGGCCAACGTGGGGA T A AC008764.1,SLC35E1 Ensembl:ENSG00000141979,Ensembl:ENSG00000127526 Protein coding,Protein coding intron,intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells chr19:16563707..16563708 23474544,24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_25388054 RMVar_hsa_circ_12003,RMVar_hsa_circ_312140,RMVar_hsa_circ_193202 52705 RMVar_ID_52705 Human_SNP_ID_833000377 A-to-I Human chr19 - 3626685 3626685 3626685 GGCCGAAGGCGGCAGAGTCAGAGCGGGAGCCGAAGTCGGAGCAGGAGCCATGGGCGGCGAAACCG GGCCGAAGGCGGCAGAGTCAGAGCGGGAGCCGGAGTCGGAGCAGGAGCCATGGGCGGCGAAACCG T C CACTIN Ensembl:ENSG00000105298 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr19:3626685..3626686 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - Human_RBP_ID_4557911,Human_RBP_ID_9381667,Human_RBP_ID_26337045 Human_Splice_Rec_1937805,Human_Splice_Rec_1937823,Human_Splice_Rec_1937845,Human_Splice_Rec_1937863 52706 RMVar_ID_52706 Human_SNP_ID_833009131 A-to-I Human chr19 + 10723932 10723932 10723932 TGGGCAACATAGACCCCGTCTCTACAAAAAATAAAAACATTAGCTGGGCATGGTGACACCTGTAG TGGGCAACATAGACCCCGTCTCTACAAAAAATTAAAACATTAGCTGGGCATGGTGACACCTGTAG A T DNM2 Ensembl:ENSG00000079805 Protein coding intron GSE100210 HepG2 cell line chr19:10723931..10723932 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - RMVar_hsa_circ_105373,RMVar_hsa_circ_192432 52707 RMVar_ID_52707 Human_SNP_ID_833014228 A-to-I Human chr19 + 40856374 40856374 40856374 GTTGCCCAGGCTGATCTTGAACTCCTGGGATCAAGTGATTCTCCTGCCTCATCCTCCCAAAGTGC GTTGCCCAGGCTGATCTTGAACTCCTGGGATCCAGTGATTCTCCTGCCTCATCCTCCCAAAGTGC A C AC008537.1 Ensembl:ENSG00000268797 Protein coding intron GSE100210 HepG2 cell line chr19:40856374..40856375 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 52708 RMVar_ID_52708 Human_SNP_ID_833045679 A-to-I Human chr19 + 45095272 45095272 45095272 CTCCTGCCTCAGCCTCCTCAGTATCTGGGATTACAGGCACCTGTCATCACACCTGGCTAAAAATG CTCCTGCCTCAGCCTCCTCAGTATCTGGGATTTCAGGCACCTGTCATCACACCTGGCTAAAAATG A T MARK4,PPP1R37 Ensembl:ENSG00000007047,Ensembl:ENSG00000104866 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line chr19:45095271..45095272 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 2 oesophagus RMVar_hsa_circ_267348 52709 RMVar_ID_52709 Human_SNP_ID_833046895 A-to-I Human chr19 + 57872942 57872942 57872942 GGCTTTTCTCCAGTGTGAACTCTCTTGTGTTTAGTGAGACTGGAGCTTTCAGCAAAAGATTTTCC GGCTTTTCTCCAGTGTGAACTCTCTTGTGTTTTGTGAGACTGGAGCTTTCAGCAAAAGATTTTCC A T - - Other Unknown GSE100210 HepG2 cell line chr19:57872941..57872942 29129909 RNA-Seq:(High) rs748331371 Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_13523911 52710 RMVar_ID_52710 Human_SNP_ID_833050668 A-to-I Human chr19 - 23361268 23361268 23361268 CCCTTACTACACATAAAATAATTCATGCTGGAAAGAAACTCTACAAATGTGAAGAATGTGGCAAA CCCTTACTACACATAAAATAATTCATGCTGGAGAGAAACTCTACAAATGTGAAGAATGTGGCAAA T C ZNF91 Ensembl:ENSG00000167232 Protein coding intron GSE107867 ASD brains,temporal_cortex chr19:23361267..23361268 30559470 RNA-Seq:(High) rs775185517 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_8096199,Human_RBP_ID_9085513 Human_miRNA_ID_217178,Human_miRNA_ID_661869,Human_miRNA_ID_668061,Human_miRNA_ID_673145 RMVar_hsa_circ_193761,RMVar_hsa_circ_193757,RMVar_hsa_circ_193758,RMVar_hsa_circ_193760,RMVar_hsa_circ_193759,RMVar_hsa_circ_193763,RMVar_hsa_circ_193764,RMVar_hsa_circ_193765,RMVar_hsa_circ_193762 52711 RMVar_ID_52711 Human_SNP_ID_833066119 A-to-I Human chr19 - 40075202 40075202 40075202 ACCTTGTTCAACATCAGAGTATTCATGCTGGTATAAAACCATATGAATGTAAGGAGTGTGGGAAA ACCTTGTTCAACATCAGAGTATTCATGCTGGTGTAAAACCATATGAATGTAAGGAGTGTGGGAAA T C ZNF780A,AC005614.2 Ensembl:ENSG00000197782,Ensembl:ENSG00000269749 Protein coding,lincRNA CDS,intron GSE107867 ASD brains,cerebellum chr19:40075201..40075202 30559470 RNA-Seq:(High) rs1429728684 Functional Loss SNV ICGC,COSMIC 33..33 33 lung adenocarcinoma,LICA 7 lung Human_miRNA_ID_1388631,Human_miRNA_ID_2120876,Human_miRNA_ID_2124092,Human_miRNA_ID_2127313,Human_miRNA_ID_2130531,Human_miRNA_ID_2924096 RMVar_hsa_circ_95105,RMVar_hsa_circ_100241,RMVar_hsa_circ_194819,RMVar_hsa_circ_372750,RMVar_hsa_circ_194820,RMVar_hsa_circ_97248,RMVar_hsa_circ_194823,RMVar_hsa_circ_78041,RMVar_hsa_circ_83137,RMVar_hsa_circ_194824,RMVar_hsa_circ_194825,RMVar_hsa_circ_194821,RMVar_hsa_circ_194822 52712 RMVar_ID_52712 Human_SNP_ID_833067626 A-to-I Human chr19 - 57789860 57789860 57789860 TGCCACCAACACCTAACTCCCCCACACCATAGACCTCTCTCTGGCCTTGCCAGAAGTTAAAGTAT TGCCACCAACACCTAACTCCCCCACACCATAGGCCTCTCTCTGGCCTTGCCAGAAGTTAAAGTAT T C - - Other Unknown GSE38233 cultured B-cells chr19:57789859..57789860 24183664 RNA-Seq:(High) rs6510097 Functional Loss SNV ICGC 33..33 33 LAML 1 - 52713 RMVar_ID_52713 Human_SNP_ID_833071108 A-to-I Human chr19 + 10109101 10109101 10109101 CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGTGCCCGCCACCACACCCCGGCTAATTTT CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTGCAGGTGCCCGCCACCACACCCCGGCTAATTTT A G PPAN,PPAN-P2RY11 Ensembl:ENSG00000130810,Ensembl:ENSG00000243207 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells chr19:10109100..10109101 24183664 RNA-Seq:(High) rs1287947847 Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 5 ovary RMVar_hsa_circ_82075,RMVar_hsa_circ_77059,RMVar_hsa_circ_192260,RMVar_hsa_circ_192261 52714 RMVar_ID_52714 Human_SNP_ID_833072031 A-to-I Human chr19 + 57860997 57860997 57860997 CTTCTGCCTCAGCCTCCCGAGTAGCAGGGATTACCGGTGTGCACCACCATGCCTGGATAACTTTT CTTCTGCCTCAGCCTCCCGAGTAGCAGGGATTTCCGGTGTGCACCACCATGCCTGGATAACTTTT A T ZNF587 Ensembl:ENSG00000198466 Protein coding 3'UTR GSE100210 HepG2 cell line chr19:57860996..57860997 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 7 liver Human_RBP_ID_528211,Human_RBP_ID_6790252 52715 RMVar_ID_52715 Human_SNP_ID_833072839 A-to-I Human chr19 + 13773604 13773604 13773604 TGTGCTTTGATTGCACTACTGCACTTCACCCTAAGCAACAGAGTGAGACCCCATCTCTTTAAAAA TGTGCTTTGATTGCACTACTGCACTTCACCCTGAGCAACAGAGTGAGACCCCATCTCTTTAAAAA A G MRI1 Ensembl:ENSG00000037757 Protein coding 3'UTR GSE47997;GSE38233;GSE38233;GSE100210;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;cultured B-cells;HepG2 cell line;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line chr19:13773603..13773604;chr19:13773604..13773605 23474544,24183664,24183664,29129909,29129909,31158229,31158229,31158229,31158229,31158229,31158229,32596459,32596459 RNA-Seq:(High) rs1241246013 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue Human_RBP_ID_26464910 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 52716 RMVar_ID_52716 Human_SNP_ID_833075381 A-to-I Human chr19 - 45855151 45855151 45855151 ACTCTGGGCCAGGCACTGTGGTTCACGCCTGTAATCCCTGCACTTTGGGAGGCCGAGGCAGGTGG ACTCTGGGCCAGGCACTGTGGTTCACGCCTGTGATCCCTGCACTTTGGGAGGCCGAGGCAGGTGG T C SYMPK Ensembl:ENSG00000125755 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr19:45855150..45855151 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 4 breast Human_RBP_ID_13477121 RMVar_hsa_circ_92180,RMVar_hsa_circ_195447 52717 RMVar_ID_52717 Human_SNP_ID_833091423 A-to-I Human chr19 + 44992878 44992878 44992878 CGAGCCCCAGGAAGCCCCTCCAAAGCCAGCAGAGGACAAGAAAAAGGATTAGTCGAGACTGGTCC CGAGCCCCAGGAAGCCCCTCCAAAGCCAGCAGTGGACAAGAAAAAGGATTAGTCGAGACTGGTCC A T CLPTM1 Ensembl:ENSG00000104853 Protein coding CDS GSE100210 HepG2 cell line chr19:44992877..44992878 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 oesophagus squamous_cell_carcinoma 12 oesophagus Human_RBP_ID_27275545 Human_miRNA_ID_655814 52718 RMVar_ID_52718 Human_SNP_ID_833093856 A-to-I Human chr19 - 3295526 3295526 3295526 GAGGTGGTGGGGGTGGGGGTGGGGCACCTGGTATGTGTTGCGCGGGGTCCCGCCAACCTCAGCCC GAGGTGGTGGGGGTGGGGGTGGGGCACCTGGTTTGTGTTGCGCGGGGTCCCGCCAACCTCAGCCC T A - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr19:3295525..3295526 30559470 RNA-Seq:(High) rs979144350 Functional Loss SNV ICGC,COSMIC 33..33 33 prostate adenocarcinoma,PBCA 4 prostate 52719 RMVar_ID_52719 Human_SNP_ID_833115732 A-to-I Human chr19 + 54203648 54203648 54203648 TACAAAAATTAGCCGAGCATGGTGGTGTGCCTATAATCCCAGCTACTCGGGAGGCTGAGGCAGGA TACAAAAATTAGCCGAGCATGGTGGTGTGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGA A G RPS9 Ensembl:ENSG00000170889 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line chr19:54203647..54203648 24183664,29129909,31158229 RNA-Seq:(High) rs1022380585 Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_103392,RMVar_hsa_circ_196228,RMVar_hsa_circ_196229,RMVar_hsa_circ_93060,RMVar_hsa_circ_269236 52720 RMVar_ID_52720 Human_SNP_ID_833117219 A-to-I Human chr19 - 16556166 16556166 16556166 CTCTGTTGCCCTGGCTGGAGTGCAGTGGTGCAATCTCAGCTCACTGCAACCTCCACCTCCCAGGT CTCTGTTGCCCTGGCTGGAGTGCAGTGGTGCAGTCTCAGCTCACTGCAACCTCCACCTCCCAGGT T C AC008764.1,SLC35E1 Ensembl:ENSG00000141979,Ensembl:ENSG00000127526 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line chr19:16556165..16556166 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - RMVar_hsa_circ_12003,RMVar_hsa_circ_312140,RMVar_hsa_circ_193202 52721 RMVar_ID_52721 Human_SNP_ID_833117737 A-to-I Human chr19 + 785504 785503 785504 TTGAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACACGCGTGTGCCACCACGCCAG TTGAGCAATTCTCCTGCCTCAGCCTCCCGAGT_GCTGGGACTACACGCGTGTGCCACCACGCCAG TA T LINC01836 Ensembl:ENSG00000267530 lincRNA exon GSE100210 HepG2 cell line chr19:785503..785504 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 33..33 33 PBCA 2 - Human_Splice_Rec_1928940 52722 RMVar_ID_52722 Human_SNP_ID_833122536 A-to-I Human chr19 - 16640175 16640175 16640175 CTACTTGGAAGGCTGACAGGAGAATCGCTTGAACCTGGGAGGCAGAGGTTGCAGTGAGCAGAGAT CTACTTGGAAGGCTGACAGGAGAATCGCTTGACCCTGGGAGGCAGAGGTTGCAGTGAGCAGAGAT T G SMIM7,AC008764.4,AC024075.1 Ensembl:ENSG00000214046,Ensembl:ENSG00000268790,Ensembl:ENSG00000267904 Protein coding,Protein coding,lincRNA intron,intron,intron GSE100210 HepG2 cell line chr19:16640174..16640175 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_349256 52723 RMVar_ID_52723 Human_SNP_ID_833122855 A-to-I Human chr19 + 50026397 50026396 50026397 TTCCTCGAACCCCCAGTCTCTACTAAAAATACAAAAATTAGTTGAGCGTGGTGGCGGGGGCCTGT TTCCTCGAACCCCCAGTCTCTACTAAAAATAC_AAAATTAGTTGAGCGTGGTGGCGGGGGCCTGT CA C ZNF473 Ensembl:ENSG00000142528 Protein coding intron GSE47997 K562 cells&HepG2 cells chr19:50026397..50026398 23474544 RNA-Seq:(High) - Functional Loss DEL ICGC 33..33 33 RECA 1 - 52724 RMVar_ID_52724 Human_SNP_ID_833126816 A-to-I Human chr19 - 51997101 51997101 51997101 TTGCCCAGGCTGGTCTCAAATTTCTGGGCTCAAGTGATCCTCTTTGCCTCACCCTACCAAAGTGC TTGCCCAGGCTGGTCTCAAATTTCTGGGCTCAGGTGATCCTCTTTGCCTCACCCTACCAAAGTGC T C ZNF615 Ensembl:ENSG00000197619 Protein coding intron GSE100210 HepG2 cell line chr19:51997100..51997101 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_196057,RMVar_hsa_circ_120306 52725 RMVar_ID_52725 Human_SNP_ID_833128033 A-to-I Human chr19 - 45847036 45847036 45847036 TAGTCCCAGCATTTTGAGAGGCCAAGGCAGGCAGATCACTTGGGGTCAGGAGTTCGAGACCACCC TAGTCCCAGCATTTTGAGAGGCCAAGGCAGGCGGATCACTTGGGGTCAGGAGTTCGAGACCACCC T C SYMPK Ensembl:ENSG00000125755 Protein coding intron GSE100210 HepG2 cell line chr19:45847035..45847036 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast lobular_carcinoma 4 breast 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 52726 RMVar_ID_52726 Human_SNP_ID_833129935 A-to-I Human chr19 - 23359502 23359502 23359502 CTTACTAACCATAAGAAAATTCATACTATCACACCTGTAATCCCACTACTTTGGGAGGCCGAGGC CTTACTAACCATAAGAAAATTCATACTATCACGCCTGTAATCCCACTACTTTGGGAGGCCGAGGC T C ZNF91 Ensembl:ENSG00000167232 Protein coding intron GSE56152;GSE107867 embryonic stem cells,wild type;ASD brains,Fragile X samples from NIH NeuroBioBank chr19:23359501..23359502 25708366,30559470 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 8 liver Human_RBP_ID_8096192,Human_RBP_ID_8831093,Human_RBP_ID_9258551,Human_RBP_ID_9291597,Human_RBP_ID_17382656,Human_RBP_ID_17918494,Human_RBP_ID_18302531 RMVar_hsa_circ_193761,RMVar_hsa_circ_193757,RMVar_hsa_circ_193758,RMVar_hsa_circ_193760,RMVar_hsa_circ_193759,RMVar_hsa_circ_193763,RMVar_hsa_circ_193764,RMVar_hsa_circ_193765,RMVar_hsa_circ_193762 52727 RMVar_ID_52727 Human_SNP_ID_833143826 A-to-I Human chr19 + 52556196 52556196 52556196 TGTTAAGAGGATGGGGCCAGGTGTGGTGGCTCAGGCCTGTAATCCCAGCACGTTGGAAGACCAAG TGTTAAGAGGATGGGGCCAGGTGTGGTGGCTCGGGCCTGTAATCCCAGCACGTTGGAAGACCAAG A G ZNF808,ZNF701 Ensembl:ENSG00000198482,Ensembl:ENSG00000167562 Protein coding,Protein coding intron,3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr19:52556195..52556196 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 haematopoietic and lymphoid tissue RMVar_hsa_circ_116818,RMVar_hsa_circ_196155 52728 RMVar_ID_52728 Human_SNP_ID_833152407 A-to-I Human chr19 - 23661528 23661528 23661528 GTGCCACCACACCCGGCTAATTTTGTGTTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGC GTGCCACCACACCCGGCTAATTTTGTGTTTTTTGTAGAGATGGGGTTTCACCATGTTGGCCAGGC T A ZNF675 Ensembl:ENSG00000197372 Protein coding intron GSE38233 cultured B-cells chr19:23661527..23661528 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_193775,RMVar_hsa_circ_79955 52729 RMVar_ID_52729 Human_SNP_ID_833158868 A-to-I Human chr19 + 7402079 7402079 7402079 TGCCACAGGCTGGGGGTAGTGGAGTGGGGAGTAATGGCCAAGGTAATGGGGTTTCTTTTTGAGGT TGCCACAGGCTGGGGGTAGTGGAGTGGGGAGTGATGGCCAAGGTAATGGGGTTTCTTTTTGAGGT A G AC008878.3,ARHGEF18 Ensembl:ENSG00000268861,Ensembl:ENSG00000104880 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells chr19:7402078..7402079 24183664 RNA-Seq:(High) rs2432103 Functional Loss SNV ICGC 33..33 33 LAML 1 - GWAS_ID_2305 RMVar_hsa_circ_191972,RMVar_hsa_circ_86296 52730 RMVar_ID_52730 Human_SNP_ID_833161408 A-to-I Human chr19 - 52883735 52883735 52883735 CACCACGTCCAGCTAATTTTTTTTGTATTTTTAATAGAGATGGGGTTTTACCATTTGTTCCAGGC CACCACGTCCAGCTAATTTTTTTTGTATTTTTGATAGAGATGGGGTTTTACCATTTGTTCCAGGC T C ZNF320 Ensembl:ENSG00000182986 Protein coding intron GSE38233 cultured B-cells chr19:52883734..52883735 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_196178,RMVar_hsa_circ_100352,RMVar_hsa_circ_356978 52731 RMVar_ID_52731 Human_SNP_ID_833162120 A-to-I Human chr19 + 57843089 57843089 57843089 GCGATCGTAGCTCACTGCATCCTCCGCCCCCTAGGCTCAAGTGATCTTCCCACCTTAGCCTCCAT GCGATCGTAGCTCACTGCATCCTCCGCCCCCTGGGCTCAAGTGATCTTCCCACCTTAGCCTCCAT A G AC010522.1,ZNF587B Ensembl:ENSG00000268750,Ensembl:ENSG00000269343 Protein coding,Protein coding intron,3'UTR GSE100210 HepG2 cell line chr19:57843088..57843089 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_13522945 RMVar_hsa_circ_196453,RMVar_hsa_circ_121905,RMVar_hsa_circ_112355,RMVar_hsa_circ_115228,RMVar_hsa_circ_196457,RMVar_hsa_circ_196458 52732 RMVar_ID_52732 Human_SNP_ID_833164459 A-to-I Human chr19 + 3448142 3448142 3448142 TAGCCCTGGCTGGAGTGTAGTGGCGTGATCTCAGCTCACTGCAACCTCTGCCTCCTGGGTTCAAG TAGCCCTGGCTGGAGTGTAGTGGCGTGATCTCGGCTCACTGCAACCTCTGCCTCCTGGGTTCAAG A G NFIC Ensembl:ENSG00000141905 Protein coding intron GSE100210 HepG2 cell line chr19:3448141..3448142 29129909 RNA-Seq:(High) rs1293741760 Functional Loss SNV ICGC 33..33 33 PRAD 1 - 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 52733 RMVar_ID_52733 Human_SNP_ID_833169174 A-to-I Human chr19 + 45670211 45670211 45670211 CTCCACCATGCCTGGCTAATTTTTGGATTTTTAGTAGAGACGGGGATTTCACCATGTTGGTCAGG CTCCACCATGCCTGGCTAATTTTTGGATTTTTGGTAGAGACGGGGATTTCACCATGTTGGTCAGG A G GIPR Ensembl:ENSG00000010310 Protein coding intron GSE38233 cultured B-cells chr19:45670210..45670211 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 52734 RMVar_ID_52734 Human_SNP_ID_833186371 A-to-I Human chr19 + 57364842 57364842 57364842 TGCAGGAGCCATATATTGAAGACCATGTCTGGAAGCTTCTACTTTGTAATTGTTGGTCACCATGA TGCAGGAGCCATATATTGAAGACCATGTCTGGGAGCTTCTACTTTGTAATTGTTGGTCACCATGA A G TRAPPC2B,AC003002.1,ZNF547 Ensembl:ENSG00000256060,Ensembl:ENSG00000268133,Ensembl:ENSG00000152433 Protein coding,Protein coding,Protein coding CDS,intron,intron GSE100210 HepG2 cell line chr19:57364841..57364842 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 10 haematopoietic and lymphoid tissue Human_RBP_ID_1892395,Human_RBP_ID_18740362,Human_RBP_ID_22503821 Human_Splice_Rec_2050022 52735 RMVar_ID_52735 Human_SNP_ID_833191747 A-to-I Human chr19 - 49869597 49869597 49869597 GGGTCAACTCCTTTGTTTTCCGCCTAGCGACAAGGGATTTGCTCGCACGGCATTGGCTCCATCCC GGGTCAACTCCTTTGTTTTCCGCCTAGCGACAGGGGATTTGCTCGCACGGCATTGGCTCCATCCC T C PNKP,AKT1S1 Ensembl:ENSG00000039650,Ensembl:ENSG00000204673 Protein coding,Protein coding intron,3'UTR GSE112787 293 Flip-In T-REx cells,empty vector chr19:49869596..49869597 29967493 RNA-Seq:(High) rs1159767003 Functional Loss SNV ICGC 33..33 33 PRAD 1 - Human_RBP_ID_240814,Human_RBP_ID_525684,Human_RBP_ID_1569940,Human_RBP_ID_1891064,Human_RBP_ID_5261676,Human_RBP_ID_6779379,Human_RBP_ID_17270295,Human_RBP_ID_17385176,Human_RBP_ID_17501215,Human_RBP_ID_27682037 Human_miRNA_ID_444781,Human_miRNA_ID_544317,Human_miRNA_ID_579554,Human_miRNA_ID_2142651,Human_miRNA_ID_3046460 RMVar_hsa_circ_127542,RMVar_hsa_circ_195962 52736 RMVar_ID_52736 Human_SNP_ID_833197902 A-to-I Human chr19 - 9646972 9646938 9646973 GAGTTCGAGACCAGCCTGGCCAATGCGGTGAAACTTTTGTCTCTACTAAAAATTCAAAAAATAAA GAGTTCGAGACCAGCCTGGCCAATGCGGTGA__________________________________ ATTTTATTTTTTGAATTTTTAGTAGAGACAAAAGTT A ZNF562 Ensembl:ENSG00000171466 Protein coding 3'UTR GSE100210 HepG2 cell line chr19:9646971..9646972 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 32..65 33 LICA 1 - RMVar_hsa_circ_127779,RMVar_hsa_circ_192224,RMVar_hsa_circ_192227 52737 RMVar_ID_52737 Human_SNP_ID_833198670 A-to-I Human chr19 - 19786351 19786351 19786351 CGCACTTGTTGCCCAGGCTGGAGTGCAATGGTACAATCTCGGCTCACTGCAACCTCCGCCTCCCA CGCACTTGTTGCCCAGGCTGGAGTGCAATGGTGCAATCTCGGCTCACTGCAACCTCCGCCTCCCA T C AC011477.3,ZNF506 Ensembl:ENSG00000267581,Ensembl:ENSG00000081665 lincRNA,Protein coding intron,3'UTR GSE38233;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;Bronchiolar epithelium,BERP35T4 cell line chr19:19786350..19786351 24183664,31158229 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_114335,RMVar_hsa_circ_193689,RMVar_hsa_circ_90759,RMVar_hsa_circ_193688 52738 RMVar_ID_52738 Human_SNP_ID_833217803 A-to-I Human chr19 - 36524314 36524314 36524314 AAAATTAGCCAGGTGTGGTGGCGGGCGCCTGTAGTTCCAGCTACTCAGGAGGCTGAGGTGGGAGA AAAATTAGCCAGGTGTGGTGGCGGGCGCCTGTGGTTCCAGCTACTCAGGAGGCTGAGGTGGGAGA T C ZNF260 Ensembl:ENSG00000254004 Protein coding intron GSE100210 HepG2 cell line chr19:36524313..36524314 29129909 RNA-Seq:(High) rs918696309 Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 5 ovary RMVar_hsa_circ_194417,RMVar_hsa_circ_121682 52739 RMVar_ID_52739 Human_SNP_ID_833219371 A-to-I Human chr19 - 10169549 10169549 10169549 TATTTATTTACTTATTTATTTTTTGAGACGGAATCTCGCTCTTGTCGCCCAGGCTGGAGTGCAGT TATTTATTTACTTATTTATTTTTTGAGACGGAGTCTCGCTCTTGTCGCCCAGGCTGGAGTGCAGT T C DNMT1 Ensembl:ENSG00000130816 Protein coding intron GSE38233 cultured B-cells chr19:10169548..10169549 24183664 RNA-Seq:(High) rs1353009116 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue Human_RBP_ID_13356532 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_378899,RMVar_hsa_circ_323045,RMVar_hsa_circ_61383,RMVar_hsa_circ_192310,RMVar_hsa_circ_364236,RMVar_hsa_circ_59709,RMVar_hsa_circ_303974,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_268592,RMVar_hsa_circ_192317 52740 RMVar_ID_52740 Human_SNP_ID_833223756 A-to-I Human chr19 + 18366550 18366550 18366550 TAGAGTGCAATGGCGTGATCTCGGCTCACTGCAACCTCCACCTCCTGGGTTTACACAATTCTCCT TAGAGTGCAATGGCGTGATCTCGGCTCACTGCGACCTCCACCTCCTGGGTTTACACAATTCTCCT A G PGPEP1 Ensembl:ENSG00000130517 Protein coding 3'UTR GSE100210 HepG2 cell line chr19:18366550..18366551 29129909 RNA-Seq:(High) rs529858421 Functional Loss SNV ICGC 33..33 33 LAML 1 - RMVar_hsa_circ_108567,RMVar_hsa_circ_193465 52741 RMVar_ID_52741 Human_SNP_ID_833239079 A-to-I Human chr19 - 49867151 49867151 49867151 GGCCGCTTGTGGCTCGAGAGCCCCCCTGGGGGAGCGCCCCCCATCTTCCTGCCCTCGGACGGGCA GGCCGCTTGTGGCTCGAGAGCCCCCCTGGGGGGGCGCCCCCCATCTTCCTGCCCTCGGACGGGCA T C PNKP Ensembl:ENSG00000039650 Protein coding CDS GSE100210 HepG2 cell line chr19:49867150..49867151 29129909 RNA-Seq:(High) rs757978147 Functional Loss SNV ICGC 33..33 33 SKCA 2 - Human_RBP_ID_22070457 Human_Splice_Rec_2033175,Human_Splice_Rec_2033203,Human_Splice_Rec_2033234,Human_Splice_Rec_2033235,Human_Splice_Rec_2033264,Human_Splice_Rec_2033265,Human_Splice_Rec_2033301,Human_Splice_Rec_2033329,Human_Splice_Rec_2033360,Human_Splice_Rec_2033361,Human_Splice_Rec_2033452,Human_Splice_Rec_2033453,Human_Splice_Rec_2033466,Human_Splice_Rec_2033467,Human_Splice_Rec_2033477,Human_Splice_Rec_2033486,Human_Splice_Rec_2033487,Human_Splice_Rec_2033496,Human_Splice_Rec_2033497,Human_Splice_Rec_2033499,Human_Splice_Rec_2033502,Human_Splice_Rec_2033503,Human_Splice_Rec_2033506,Human_Splice_Rec_2033510 52742 RMVar_ID_52742 Human_SNP_ID_833252891 A-to-I Human chr19 + 18366892 18366892 18366892 TATCCTCATGTGGGCTAGGTGTGGTTACTCACACCTGTAATCCTAGCACTTTGGGAGGTTGAGGC TATCCTCATGTGGGCTAGGTGTGGTTACTCACGCCTGTAATCCTAGCACTTTGGGAGGTTGAGGC A G PGPEP1 Ensembl:ENSG00000130517 Protein coding 3'UTR GSE47997;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;esophageal squamous carcinoma cells,KYSE180 cell line chr19:18366891..18366892 23474544,32596459 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_17567986,Human_RBP_ID_26472245 RMVar_hsa_circ_108567,RMVar_hsa_circ_193465 52743 RMVar_ID_52743 Human_SNP_ID_833266840 A-to-I Human chr19 + 18173937 18173937 18173937 GCGGCGGTGCAGGCGTCCCCTCTGCAAGCGTTAGACTTCTTTGGGAATGGGCCACCAGTTAACTA GCGGCGGTGCAGGCGTCCCCTCTGCAAGCGTTGGACTTCTTTGGGAATGGGCCACCAGTTAACTA A G IFI30,AC007192.1 Ensembl:ENSG00000216490,Ensembl:ENSG00000268173 Protein coding,Protein coding CDS,3'UTR GSE100210 HepG2 cell line chr19:18173936..18173937 29129909 RNA-Seq:(High) rs11554160 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue Human_RBP_ID_54731,Human_RBP_ID_4509999,Human_RBP_ID_22447558,Human_RBP_ID_22763953 Human_Splice_Rec_1979317,Human_Splice_Rec_1979465,Human_Splice_Rec_1979467 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_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_193451 52744 RMVar_ID_52744 Human_SNP_ID_833267480 A-to-I Human chr19 - 51336438 51336438 51336438 GTGATTCTCCTGCCTCAGCCTCCCGAGTAGCTAGGATTACAGTCATGCGCCACCACACCCAGCTA GTGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGTCATGCGCCACCACACCCAGCTA T C VSIG10L Ensembl:ENSG00000186806 Protein coding intron GSE100210 HepG2 cell line chr19:51336437..51336438 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 2 liver 52745 RMVar_ID_52745 Human_SNP_ID_833276867 A-to-I Human chr19 + 47177436 47177436 47177436 GCTGGAGTGTGGTGGCACAATCATAACTCACTATAGCCTTGAACTCCTGGGCTCAAGTTATCCTC GCTGGAGTGTGGTGGCACAATCATAACTCACTGTAGCCTTGAACTCCTGGGCTCAAGTTATCCTC A G SAE1 Ensembl:ENSG00000142230 Protein coding intron GSE100210 HepG2 cell line chr19:47177435..47177436 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_44245,RMVar_hsa_circ_337323,RMVar_hsa_circ_56834,RMVar_hsa_circ_195562,RMVar_hsa_circ_336917,RMVar_hsa_circ_347680,RMVar_hsa_circ_118551 52746 RMVar_ID_52746 Human_SNP_ID_833278028 A-to-I Human chr19 - 39332891 39332891 39332891 ACTTTGGGAGGTCAAGGAGGGTGGATCACTTGAGGTCAGGAGTTCAAGACTAGCCTGACCAACAT ACTTTGGGAGGTCAAGGAGGGTGGATCACTTGGGGTCAGGAGTTCAAGACTAGCCTGACCAACAT T C GMFG Ensembl:ENSG00000130755 Protein coding intron GSE38233 cultured B-cells chr19:39332890..39332891 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 9 haematopoietic and lymphoid tissue RMVar_hsa_circ_341129 52747 RMVar_ID_52747 Human_SNP_ID_833287349 A-to-I Human chr19 + 49088071 49088071 49088071 GCACCACCACGCCTGGCTAATTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTAGGCCAGGC GCACCACCACGCCTGGCTAATTTTGTATTTTTCGTAGAGATGGGGTTTCACCATGTAGGCCAGGC A C SNRNP70 Ensembl:ENSG00000104852 Protein coding intron GSE38233 cultured B-cells chr19:49088070..49088071 24183664 RNA-Seq:(High) rs546705306 Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_12770,RMVar_hsa_circ_369857,RMVar_hsa_circ_195801 52748 RMVar_ID_52748 Human_SNP_ID_833299018 A-to-I Human chr19 - 45726780 45726779 45726781 GGTACTGAGGCTGGGCAAGGTGGCTCATGCTTATAATCTTGGCACTTTGGGAGGCCAAGGTGGGA GGTACTGAGGCTGGGCAAGGTGGCTCATGCT__TAATCTTGGCACTTTGGGAGGCCAAGGTGGGA ATA A FBXO46 Ensembl:ENSG00000177051 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr19:45726779..45726780 24183664,29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 32..33 33 SKCA 1 - Human_RBP_ID_25447198 52749 RMVar_ID_52749 Human_SNP_ID_833303809 A-to-I Human chr19 - 33172833 33172833 33172833 CGCCTGCTTCAGCCTCCCAAAATGTTGGGATTACAGGCGTGAAACACCGCATCCAGCTGGAAGTT CGCCTGCTTCAGCCTCCCAAAATGTTGGGATTGCAGGCGTGAAACACCGCATCCAGCTGGAAGTT T C HSALNG0125414 RNACentral:URS0000EA4FA0 lincRNA intron GSE100210 HepG2 cell line chr19:33172832..33172833 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 RECA 1 - 52750 RMVar_ID_52750 Human_SNP_ID_833317421 A-to-I Human chr19 - 54444590 54444590 54444590 TCGGCTCACTCCAACCTCCGCCTCCCGGGTTCAAGCAATTCTTCTGCCTCAGCCTCCCGAGTAGC TCGGCTCACTCCAACCTCCGCCTCCCGGGTTCCAGCAATTCTTCTGCCTCAGCCTCCCGAGTAGC T G LENG8-AS1,LENG8-AS1:2,LENG8-AS1:3,LENG8-AS1:4 RNACentral:URS0000D5B63F,RNACentral:URS00009B73B1,RNACentral:URS00009C0486,RNACentral:URS00009C1D5E lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,exon GSE100210 HepG2 cell line chr19:54444589..54444590 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 OV 1 - 52751 RMVar_ID_52751 Human_SNP_ID_833319175 A-to-I Human chr19 - 57941243 57941243 57941243 AGTTCACACTGGAGAAAGGCCTTATGAGTGCAATGAATGTGGGAAGTTTTTTAGCCAGAGCTCCA AGTTCACACTGGAGAAAGGCCTTATGAGTGCAGTGAATGTGGGAAGTTTTTTAGCCAGAGCTCCA T C ZNF256 Ensembl:ENSG00000152454 Protein coding CDS GSE107867 ASD brains,frontal_cortex chr19:57941242..57941243 30559470 RNA-Seq:(High) rs758292773 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_23809687 52752 RMVar_ID_52752 Human_SNP_ID_833324954 A-to-I Human chr19 + 13772617 13772617 13772617 TTGGGAGGCCGAGGCAGGTGGATCACAAGATCAGGAGATTGAGACCATCCTGGCTAACATGGTGA TTGGGAGGCCGAGGCAGGTGGATCACAAGATCGGGAGATTGAGACCATCCTGGCTAACATGGTGA A G MRI1 Ensembl:ENSG00000037757 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line chr19:13772616..13772617 24183664,31158229,31158229,31158229 RNA-Seq:(High) rs1342386386 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue 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 52753 RMVar_ID_52753 Human_SNP_ID_833359254 A-to-I Human chr19 - 43663257 43663257 43663257 ACCCATCCATCACCAGACAGTGACTGATTATTAGGTTAATGCAAAAGTAATTGTGGCTTTTGCCA ACCCATCCATCACCAGACAGTGACTGATTATTTGGTTAATGCAAAAGTAATTGTGGCTTTTGCCA T A PLAUR Ensembl:ENSG00000011422 Protein coding intron GSE100210 HepG2 cell line chr19:43663256..43663257 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LMS 1 - Human_RBP_ID_1094151 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 52754 RMVar_ID_52754 Human_SNP_ID_833366704 A-to-I Human chr19 + 13772565 13772565 13772565 AAATGTGGATAACAGGCCGGGCGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAG AAATGTGGATAACAGGCCGGGCGCAGTGGCTCGCACCTGTAATCCCAGCACTTTGGGAGGCCGAG A G MRI1 Ensembl:ENSG00000037757 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr19:13772564..13772565 24183664,29129909 RNA-Seq:(High) - 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 52755 RMVar_ID_52755 Human_SNP_ID_833378248 A-to-I Human chr19 - 45884046 45884046 45884046 GCGAGATCGCCACCATCCTTGCTGGAGACATCAAAGTTAAGAAAGAACGGGACCCCTAGGCTACC GCGAGATCGCCACCATCCTTGCTGGAGACATCGAAGTTAAGAAAGAACGGGACCCCTAGGCTACC T C IRF2BP1 Ensembl:ENSG00000170604 Protein coding CDS GSE100210 HepG2 cell line chr19:45884045..45884046 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 skin desmoplastic 1 skin Human_RBP_ID_13477479,Human_RBP_ID_18736037 52756 RMVar_ID_52756 Human_SNP_ID_833390695 A-to-I Human chr19 - 38868512 38868512 38868512 CCCCTGCCTCTGCCTACCAAGTAGCTGAGACTACAGGCACCTACCACCGTGCCTGTCTAATTTTT CCCCTGCCTCTGCCTACCAAGTAGCTGAGACTGCAGGCACCTACCACCGTGCCTGTCTAATTTTT T C RINL Ensembl:ENSG00000187994 Protein coding 3'UTR GSE38233 cultured B-cells chr19:38868511..38868512 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 52757 RMVar_ID_52757 Human_SNP_ID_833392999 A-to-I Human chr19 - 10495100 10495100 10495100 AAAATTAGCCGGGTGTGGTTGTGCGTGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCTGAGGC AAAATTAGCCGGGTGTGGTTGTGCGTGCCTGTGGTCCCAGCTACTCAGGAGGCTGAGGCTGAGGC T C KEAP1 Ensembl:ENSG00000079999 Protein coding intron GSE38233 cultured B-cells chr19:10495099..10495100 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 UTCA 1 - RMVar_hsa_circ_87608,RMVar_hsa_circ_192373 52758 RMVar_ID_52758 Human_SNP_ID_833395463 A-to-I Human chr19 - 20564097 20564096 20564097 CAGTGGCGTGATCTCGGCTTACTGCAGCCTCCACCTCCTGGGTTCAAGCAATTCTCCTGCCTCAG CAGTGGCGTGATCTCGGCTTACTGCAGCCTCC_CCTCCTGGGTTCAAGCAATTCTCCTGCCTCAG GT G AC010636.2,ZNF737 Ensembl:ENSG00000269110,Ensembl:ENSG00000237440 lincRNA,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells chr19:20564096..20564097 23474544 RNA-Seq:(High) - Functional Loss DEL ICGC 33..33 33 PAAD 1 - Human_Splice_Rec_1984518 RMVar_hsa_circ_193701 52759 RMVar_ID_52759 Human_SNP_ID_833402669 A-to-I Human chr19 - 38869073 38869073 38869073 AGGGGTTTCACACCCCTCCGTTCATGCCTGTAATCCCAACATTTTGGGAGGCCAAGGTGGGAGGA AGGGGTTTCACACCCCTCCGTTCATGCCTGTAGTCCCAACATTTTGGGAGGCCAAGGTGGGAGGA T C RINL Ensembl:ENSG00000187994 Protein coding 3'UTR GSE38233 cultured B-cells chr19:38869072..38869073 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_Splice_Rec_2004172,Human_Splice_Rec_2004196,Human_Splice_Rec_2004212 52760 RMVar_ID_52760 Human_SNP_ID_833406136 A-to-I Human chr19 + 11956811 11956811 11956811 TCGGGGCGGAGGCTGCAGTGAGCCAAGATCACACCATTGCACTTCAGATTGGATGACTGAGCAAG TCGGGGCGGAGGCTGCAGTGAGCCAAGATCACGCCATTGCACTTCAGATTGGATGACTGAGCAAG A G AC008770.2 Ensembl:ENSG00000267179 Protein coding intron GSE100210 HepG2 cell line chr19:11956810..11956811 29129909 RNA-Seq:(High) rs943853191 Functional Loss SNV ICGC 33..33 33 PBCA 1 - 52761 RMVar_ID_52761 Human_SNP_ID_833411817 A-to-I Human chr19 + 48959783 48959783 48959783 GGGAGGCGGAGGTTGCAATGAGCCGAGACTGCACTATTGTACTCCAGCCTGGGCAACAAGATCAA GGGAGGCGGAGGTTGCAATGAGCCGAGACTGCGCTATTGTACTCCAGCCTGGGCAACAAGATCAA A G BAX Ensembl:ENSG00000087088 Protein coding intron GSE38233 cultured B-cells chr19:48959782..48959783 24183664 RNA-Seq:(High) rs11669164 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_25429372 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 52762 RMVar_ID_52762 Human_SNP_ID_833419956 A-to-I Human chr19 + 57840836 57840836 57840836 AACATGCACTTCACCAGCATTTTCTTGCTTTCAGGTTGTTGGTGTGGAGTGGAAGATGAGGCGGC AACATGCACTTCACCAGCATTTTCTTGCTTTCGGGTTGTTGGTGTGGAGTGGAAGATGAGGCGGC A G AC010522.1,ZNF587B Ensembl:ENSG00000268750,Ensembl:ENSG00000269343 Protein coding,Protein coding intron,intron GSE105773 Glioblastoma cells,U87MG chr19:57840835..57840836 29724793 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus RMVar_hsa_circ_196453,RMVar_hsa_circ_121905,RMVar_hsa_circ_112355,RMVar_hsa_circ_115228,RMVar_hsa_circ_196457 52763 RMVar_ID_52763 Human_SNP_ID_833419974 A-to-I Human chr19 + 57840836 57840836 57840836 AACATGCACTTCACCAGCATTTTCTTGCTTTCAGGTTGTTGGTGTGGAGTGGAAGATGAGGCGGC AACATGCACTTCACCAGCATTTTCTTGCTTTCTGGTTGTTGGTGTGGAGTGGAAGATGAGGCGGC A T AC010522.1,ZNF587B Ensembl:ENSG00000268750,Ensembl:ENSG00000269343 Protein coding,Protein coding intron,intron GSE105773 Glioblastoma cells,U87MG chr19:57840835..57840836 29724793 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_196453,RMVar_hsa_circ_121905,RMVar_hsa_circ_112355,RMVar_hsa_circ_115228,RMVar_hsa_circ_196457 52764 RMVar_ID_52764 Human_SNP_ID_833433064 A-to-I Human chr19 - 38868460 38868460 38868460 CTGTCTAATTTTTAAAATTTTTTATAAAGATGAGGTCTCTCTTTGTTGCCCAGGCTGGTCTCAAA CTGTCTAATTTTTAAAATTTTTTATAAAGATGGGGTCTCTCTTTGTTGCCCAGGCTGGTCTCAAA T C RINL Ensembl:ENSG00000187994 Protein coding 3'UTR GSE38233 cultured B-cells chr19:38868459..38868460 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 52765 RMVar_ID_52765 Human_SNP_ID_833438931 A-to-I Human chr19 + 11098088 11098088 11098088 CCAATATAGTGAAACTCCATCTCTACTAAAATACAAGAAATTACCTGGGCATGGTGGCAGTTGCT CCAATATAGTGAAACTCCATCTCTACTAAAATGCAAGAAATTACCTGGGCATGGTGGCAGTTGCT A G LDLR Ensembl:ENSG00000130164 Protein coding intron GSE38233 cultured B-cells chr19:11098087..11098088 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 52766 RMVar_ID_52766 Human_SNP_ID_833469711 A-to-I Human chr19 + 38630595 38630595 38630595 CTCGATCTCCTGACCTCACGATCGCCCGTCTCAGCCTCCCCAAGTGCTGGGATTACAGGTTTGAG CTCGATCTCCTGACCTCACGATCGCCCGTCTCTGCCTCCCCAAGTGCTGGGATTACAGGTTTGAG A T EIF3K Ensembl:ENSG00000178982 Protein coding intron GSE100210 HepG2 cell line chr19:38630594..38630595 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 8 ovary Human_RBP_ID_13448838 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 52767 RMVar_ID_52767 Human_SNP_ID_833482323 A-to-I Human chr19 + 38631025 38631025 38631025 TAGAGACAGGGTTTCACCCTGTTGGCCAGGGTAGTCTCGAACTCCTGACCTCAAGTGATCCACCC TAGAGACAGGGTTTCACCCTGTTGGCCAGGGTGGTCTCGAACTCCTGACCTCAAGTGATCCACCC A G EIF3K Ensembl:ENSG00000178982 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line chr19:38631024..38631025 24183664,31158229 RNA-Seq:(High) rs538323347 Functional Loss SNV ICGC 33..33 33 PBCA 1 - 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 52768 RMVar_ID_52768 Human_SNP_ID_833496448 A-to-I Human chr19 + 50395437 50395437 50395437 AACCCCGTCTCTACTAAAAATACAAAAAAATTAGGCGGGCGCAGTGGCGGACGCCTGTAGTCCCA AACCCCGTCTCTACTAAAAATACAAAAAAATTTGGCGGGCGCAGTGGCGGACGCCTGTAGTCCCA A T POLD1 Ensembl:ENSG00000062822 Protein coding intron GSE100210 HepG2 cell line chr19:50395436..50395437 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BOCA 1 - RMVar_hsa_circ_76877,RMVar_hsa_circ_195992 52769 RMVar_ID_52769 Human_SNP_ID_833509010 A-to-I Human chr19 + 34433812 34433812 34433812 TGAAACCGTCTCTACCAAAAAACACAAAAATTAGCCGGTGTGGTGGCATGTGCCTGTAGTCCCAG TGAAACCGTCTCTACCAAAAAACACAAAAATTTGCCGGTGTGGTGGCATGTGCCTGTAGTCCCAG A T UBA2 Ensembl:ENSG00000126261 Protein coding intron GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line chr19:34433811..34433812 23474544,24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_93128,RMVar_hsa_circ_54140,RMVar_hsa_circ_125569,RMVar_hsa_circ_194114,RMVar_hsa_circ_279072,RMVar_hsa_circ_353894,RMVar_hsa_circ_69805,RMVar_hsa_circ_194110,RMVar_hsa_circ_363447,RMVar_hsa_circ_291250,RMVar_hsa_circ_312685,RMVar_hsa_circ_276563,RMVar_hsa_circ_276657,RMVar_hsa_circ_275866,RMVar_hsa_circ_21381,RMVar_hsa_circ_194115,RMVar_hsa_circ_285792,RMVar_hsa_circ_310937,RMVar_hsa_circ_194112,RMVar_hsa_circ_194113,RMVar_hsa_circ_194111,RMVar_hsa_circ_356926,RMVar_hsa_circ_290880,RMVar_hsa_circ_288581,RMVar_hsa_circ_281045,RMVar_hsa_circ_285276,RMVar_hsa_circ_273262,RMVar_hsa_circ_194121,RMVar_hsa_circ_194125,RMVar_hsa_circ_119372,RMVar_hsa_circ_194126,RMVar_hsa_circ_194123,RMVar_hsa_circ_194124,RMVar_hsa_circ_194122,RMVar_hsa_circ_300968,RMVar_hsa_circ_194119,RMVar_hsa_circ_194120,RMVar_hsa_circ_313831,RMVar_hsa_circ_346878,RMVar_hsa_circ_368008,RMVar_hsa_circ_315612,RMVar_hsa_circ_301892,RMVar_hsa_circ_270348,RMVar_hsa_circ_288271,RMVar_hsa_circ_104307,RMVar_hsa_circ_194130,RMVar_hsa_circ_194132,RMVar_hsa_circ_194133,RMVar_hsa_circ_194131,RMVar_hsa_circ_194129 52770 RMVar_ID_52770 Human_SNP_ID_833511993 A-to-I Human chr19 - 9767163 9767163 9767163 GCAATGCACTACAGCCTGGGCAACAAGAGCAAAACACCGTCTAAATAAATAAATAAATAAATAAA GCAATGCACTACAGCCTGGGCAACAAGAGCAAGACACCGTCTAAATAAATAAATAAATAAATAAA T C ZNF846 Ensembl:ENSG00000196605 Protein coding intron GSE100210 HepG2 cell line chr19:9767162..9767163 29129909 RNA-Seq:(High) rs1391020223 Functional Loss SNV ICGC 33..33 33 PBCA 1 - 52771 RMVar_ID_52771 Human_SNP_ID_833527259 A-to-I Human chr19 + 17934727 17934727 17934727 ATCACTTGAGCCCAGGAGGTCAAGGCTGCAGTAAGCCGAGATTTCGCCACTGCACTCCAGCCTGG ATCACTTGAGCCCAGGAGGTCAAGGCTGCAGTGAGCCGAGATTTCGCCACTGCACTCCAGCCTGG A G CCDC124 Ensembl:ENSG00000007080 Protein coding intron GSE38233 cultured B-cells chr19:17934726..17934727 24183664 RNA-Seq:(High) rs1418127685 Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_193405,RMVar_hsa_circ_116213 52772 RMVar_ID_52772 Human_SNP_ID_833547944 A-to-I Human chr19 + 57873344 57873344 57873344 CATTCCCTACATACATAAGGTCTTTCTCCAGTATGGCCATGCTGGTGTAGAATGAGGTTACCCTT CATTCCCTACATACATAAGGTCTTTCTCCAGTGTGGCCATGCTGGTGTAGAATGAGGTTACCCTT A G - - Other Unknown GSE100210 HepG2 cell line chr19:57873343..57873344 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 8 haematopoietic and lymphoid tissue 52773 RMVar_ID_52773 Human_SNP_ID_833552256 A-to-I Human chr19 + 13924573 13924573 13924573 CTCACTTCAACCTCTGCCTCCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCAAATAGCTGGG CTCACTTCAACCTCTGCCTCCCAGGTTCAAGCCATTCTCCTGCCTCAGCCTCCCAAATAGCTGGG A C CC2D1A Ensembl:ENSG00000132024 Protein coding intron GSE38233 cultured B-cells chr19:13924573..13924574 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 STAD 1 - RMVar_hsa_circ_76281,RMVar_hsa_circ_107714,RMVar_hsa_circ_101859,RMVar_hsa_circ_192943,RMVar_hsa_circ_192946,RMVar_hsa_circ_192948 52774 RMVar_ID_52774 Human_SNP_ID_833552988 A-to-I Human chr19 - 18908187 18908187 18908187 TGGGCTTAAGCGATCCTGCCTTGGCCTCCCAAAGCGCTGGGGTTACAGGTGTGAGCCACAGTACC TGGGCTTAAGCGATCCTGCCTTGGCCTCCCAAGGCGCTGGGGTTACAGGTGTGAGCCACAGTACC T C AC002985.1,COPE Ensembl:ENSG00000268193,Ensembl:ENSG00000105669 Protein coding,Protein coding intron,intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line chr19:18908186..18908187 32596459 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 5 haematopoietic and lymphoid tissue Human_RBP_ID_17567999 RMVar_hsa_circ_193546,RMVar_hsa_circ_86189,RMVar_hsa_circ_331899,RMVar_hsa_circ_193549,RMVar_hsa_circ_104727 52775 RMVar_ID_52775 Human_SNP_ID_833561597 A-to-I Human chr19 - 18908841 18908841 18908841 GGCACGCATCACCATGCCTGGCTAATTTGTATATTTTTTAGAGATGGGGTTTTGCCTGGCCGGGC GGCACGCATCACCATGCCTGGCTAATTTGTATGTTTTTTAGAGATGGGGTTTTGCCTGGCCGGGC T C AC002985.1,COPE Ensembl:ENSG00000268193,Ensembl:ENSG00000105669 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells chr19:18908840..18908841 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 5 ovary RMVar_hsa_circ_193546,RMVar_hsa_circ_86189,RMVar_hsa_circ_331899,RMVar_hsa_circ_193549,RMVar_hsa_circ_104727 52776 RMVar_ID_52776 Human_SNP_ID_833581301 A-to-I Human chr19 + 3295527 3295527 3295527 GGCTGAGGTTGGCGGGACCCCGCGCAACACATACCAGGTGCCCCACCCCCACCCCCACCACCTCC GGCTGAGGTTGGCGGGACCCCGCGCAACACATTCCAGGTGCCCCACCCCCACCCCCACCACCTCC A T CELF5 Ensembl:ENSG00000161082 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr19:3295526..3295527 30559470 RNA-Seq:(High) rs571373340 Functional Loss SNV ICGC,COSMIC 33..33 33 prostate adenocarcinoma,PEME 3 prostate GWAS_ID_2284,GWAS_ID_2285,GWAS_ID_2286,GWAS_ID_2287,GWAS_ID_2288 52777 RMVar_ID_52777 Human_SNP_ID_833587893 A-to-I Human chr19 - 52810650 52810650 52810650 CTCTAGCCCGGCCCCTGTAGACGCGACCCCAGAGCCTGCTGTTAAAACCACTGTAGAATGGAGAG CTCTAGCCCGGCCCCTGTAGACGCGACCCCAGGGCCTGCTGTTAAAACCACTGTAGAATGGAGAG T C ZNF28 Ensembl:ENSG00000198538 Protein coding intron GSE100210 HepG2 cell line chr19:52810649..52810650 29129909 RNA-Seq:(High) rs879080730 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue RMVar_hsa_circ_60331 52778 RMVar_ID_52778 Human_SNP_ID_833606755 A-to-I Human chr19 - 51361346 51361346 51361346 CCTTGGCTGTCCTGCTTGCTGAGTGCCCTAGCACGTGCCCAGGGACTCGCTTGACAGAAAAGCCT CCTTGGCTGTCCTGCTTGCTGAGTGCCCTAGCGCGTGCCCAGGGACTCGCTTGACAGAAAAGCCT T C ETFB,AC008750.8 Ensembl:ENSG00000105379,Ensembl:ENSG00000269403 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells chr19:51361345..51361346 24183664 RNA-Seq:(High) rs4802790 Functional Loss SNV ICGC 33..33 33 LAML 1 - 52779 RMVar_ID_52779 Human_SNP_ID_833611673 A-to-I Human chr19 + 57685341 57685341 57685341 GGAGCTCCTTGATGAGTCTCAGAGGTTCCTGTACTGCGATGTGATGCTGGAGAACTTTGCACATG GGAGCTCCTTGATGAGTCTCAGAGGTTCCTGTGCTGCGATGTGATGCTGGAGAACTTTGCACATG A G AC003006.1,ZNF551 Ensembl:ENSG00000269026,Ensembl:ENSG00000204519 Protein coding,Protein coding intron,CDS GSE38233 cultured B-cells chr19:57685340..57685341 24183664 RNA-Seq:(High) rs1368134462 Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 3 lung Human_RBP_ID_1572967,Human_RBP_ID_1892618,Human_RBP_ID_18740628,Human_RBP_ID_23809363 Human_Splice_Rec_2050590,Human_Splice_Rec_2050591,Human_Splice_Rec_2050594,Human_Splice_Rec_2050595,Human_Splice_Rec_2050600,Human_Splice_Rec_2050601 Human_miRNA_ID_1541688,Human_miRNA_ID_1595130,Human_miRNA_ID_2442451 RMVar_hsa_circ_196433,RMVar_hsa_circ_104849 52780 RMVar_ID_52780 Human_SNP_ID_833613519 A-to-I Human chr19 + 14070540 14070540 14070540 CCGCCAGGAGAACGGCGCCAGCGTGATCCTCCATGACATTGTGAGAGCCAGAGAGAACATCCAGA CCGCCAGGAGAACGGCGCCAGCGTGATCCTCCGTGACATTGTGAGAGCCAGAGAGAACATCCAGA A G EEF1DP1 Ensembl:ENSG00000228887 Pseudogene exon GSE100210 HepG2 cell line chr19:14070539..14070540 29129909 RNA-Seq:(High) rs879252059 Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_6796980 Human_miRNA_ID_1829726 52781 RMVar_ID_52781 Human_SNP_ID_833629402 A-to-I Human chr19 + 37916088 37916088 37916088 TCACTCTGTTGCCCAGGCTGGAGTATAGTGGTATGATCACAGCTCACTGCAACCTCTGCCTCCTG TCACTCTGTTGCCCAGGCTGGAGTATAGTGGTGTGATCACAGCTCACTGCAACCTCTGCCTCCTG A G SIPA1L3 Ensembl:ENSG00000105738 Protein coding intron GSE38233 cultured B-cells chr19:37916087..37916088 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 3 pancreas RMVar_hsa_circ_89034,RMVar_hsa_circ_194517 52782 RMVar_ID_52782 Human_SNP_ID_833635912 A-to-I Human chr19 + 40830271 40830271 40830271 AATTTTTTTTCTTTTTCTTTTAAGACCGTCTCACTCTGTCTTTCAGGCTGCAGTGCAGTAGGGCA AATTTTTTTTCTTTTTCTTTTAAGACCGTCTCCCTCTGTCTTTCAGGCTGCAGTGCAGTAGGGCA A C AC008537.1 Ensembl:ENSG00000268797 Protein coding intron GSE100210 HepG2 cell line chr19:40830270..40830271 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 52783 RMVar_ID_52783 Human_SNP_ID_833659301 A-to-I Human chr19 - 48074427 48074427 48074427 GATACAGGCACATGTATGTTCACTGCAGCACTATTCACAATATCAAAGACATGGAATCAACCCAA GATACAGGCACATGTATGTTCACTGCAGCACTTTTCACAATATCAAAGACATGGAATCAACCCAA T A PLA2G4C Ensembl:ENSG00000105499 Protein coding intron GSE100210 HepG2 cell line chr19:48074426..48074427 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 CLLE 1 - 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_195632,RMVar_hsa_circ_195629,RMVar_hsa_circ_368767 52784 RMVar_ID_52784 Human_SNP_ID_833671665 A-to-I Human chr19 + 44172858 44172858 44172858 TTCATTTTCAACTTGTGATTTGGCATTTTCACAGGGCATCCACCCTTCAAACAAGATGTATCACC TTCATTTTCAACTTGTGATTTGGCATTTTCACCGGGCATCCACCCTTCAAACAAGATGTATCACC A C ZNF226 Ensembl:ENSG00000167380 Protein coding intron GSE105773 Glioblastoma cells,U87MG chr19:44172857..44172858 29724793 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma,lymph_node diffuse_large_B_cell_lymphoma 9 haematopoietic and lymphoid tissue Human_RBP_ID_9381092 Human_Splice_Rec_2016681,Human_Splice_Rec_2016701,Human_Splice_Rec_2016729,Human_Splice_Rec_2016747,Human_Splice_Rec_2016759,Human_Splice_Rec_2016769,Human_Splice_Rec_2016779,Human_Splice_Rec_2016819,Human_Splice_Rec_2016831,Human_Splice_Rec_2016841,Human_Splice_Rec_2016851 RMVar_hsa_circ_20511,RMVar_hsa_circ_43224,RMVar_hsa_circ_195213,RMVar_hsa_circ_327006 52785 RMVar_ID_52785 Human_SNP_ID_833673810 A-to-I Human chr19 - 9583417 9583417 9583417 GGAGGCTGAGGCAGGAGGATTGCTTGAACCTGAGAGGCCGAGGTTGCAGTGAGCCGAGATCTGCC GGAGGCTGAGGCAGGAGGATTGCTTGAACCTGGGAGGCCGAGGTTGCAGTGAGCCGAGATCTGCC T C ZNF121 Ensembl:ENSG00000197961 Protein coding intron GSE38233 cultured B-cells chr19:9583416..9583417 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_17567915 52786 RMVar_ID_52786 Human_SNP_ID_833702229 A-to-I Human chr19 - 32624926 32624926 32624926 TAAAATTAGAAAAACAAATTTTTTTTGAGACAAGATCTTGTTCTGTTGCCCAGGCTGGAGTGCAG TAAAATTAGAAAAACAAATTTTTTTTGAGACAGGATCTTGTTCTGTTGCCCAGGCTGGAGTGCAG T C ANKRD27 Ensembl:ENSG00000105186 Protein coding intron GSE100210 HepG2 cell line chr19:32624925..32624926 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_8062,RMVar_hsa_circ_126745,RMVar_hsa_circ_105380,RMVar_hsa_circ_78380,RMVar_hsa_circ_193873,RMVar_hsa_circ_193874,RMVar_hsa_circ_193875,RMVar_hsa_circ_326869,RMVar_hsa_circ_371131,RMVar_hsa_circ_50075,RMVar_hsa_circ_193876,RMVar_hsa_circ_82283,RMVar_hsa_circ_193881,RMVar_hsa_circ_373658,RMVar_hsa_circ_44324,RMVar_hsa_circ_16359,RMVar_hsa_circ_193883,RMVar_hsa_circ_305450,RMVar_hsa_circ_320628,RMVar_hsa_circ_86158,RMVar_hsa_circ_370446,RMVar_hsa_circ_78409,RMVar_hsa_circ_193886,RMVar_hsa_circ_193888,RMVar_hsa_circ_193887,RMVar_hsa_circ_325687,RMVar_hsa_circ_372620,RMVar_hsa_circ_274414,RMVar_hsa_circ_295695,RMVar_hsa_circ_77742,RMVar_hsa_circ_193892,RMVar_hsa_circ_193894,RMVar_hsa_circ_24288,RMVar_hsa_circ_193895,RMVar_hsa_circ_193893,RMVar_hsa_circ_193891,RMVar_hsa_circ_285545,RMVar_hsa_circ_285723,RMVar_hsa_circ_285131,RMVar_hsa_circ_127725,RMVar_hsa_circ_100310,RMVar_hsa_circ_193904,RMVar_hsa_circ_127089,RMVar_hsa_circ_193896,RMVar_hsa_circ_193898,RMVar_hsa_circ_193899,RMVar_hsa_circ_193897,RMVar_hsa_circ_193903,RMVar_hsa_circ_279209,RMVar_hsa_circ_334357,RMVar_hsa_circ_20072,RMVar_hsa_circ_104569,RMVar_hsa_circ_110464,RMVar_hsa_circ_193905,RMVar_hsa_circ_193906,RMVar_hsa_circ_193907,RMVar_hsa_circ_193909,RMVar_hsa_circ_317235,RMVar_hsa_circ_366811,RMVar_hsa_circ_325481,RMVar_hsa_circ_271261,RMVar_hsa_circ_193908 52787 RMVar_ID_52787 Human_SNP_ID_833704496 A-to-I Human chr19 + 34373282 34373282 34373282 GTAGTGGCAGGCGCCCATAATTCCAGCTACTCAGGAGACTGAGGCAGCAGTATCATTTGAACCCA GTAGTGGCAGGCGCCCATAATTCCAGCTACTCGGGAGACTGAGGCAGCAGTATCATTTGAACCCA A G GPI Ensembl:ENSG00000105220 Protein coding intron GSE38233 cultured B-cells chr19:34373281..34373282 24183664 RNA-Seq:(High) rs1158684543 Functional Loss SNV ICGC 33..33 33 MALY 1 - 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_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_194082,RMVar_hsa_circ_194083 52788 RMVar_ID_52788 Human_SNP_ID_833706458 A-to-I Human chr19 + 35575765 35575765 35575765 CTGGAGCATCAGGCCCATACCCGGCCATCGCCAGCAGTCAATGGAATGTGAGTGCCTTAGAGGTC CTGGAGCATCAGGCCCATACCCGGCCATCGCCGGCAGTCAATGGAATGTGAGTGCCTTAGAGGTC A G AD000090.1 Ensembl:ENSG00000283907 lincRNA exon GSE100210 HepG2 cell line chr19:35575764..35575765 29129909 RNA-Seq:(High) rs79382536 Functional Loss SNV ICGC 33..33 33 LICA 2 - Human_RBP_ID_270008,Human_RBP_ID_1064019,Human_RBP_ID_5194225,Human_RBP_ID_8103461,Human_RBP_ID_26467463 52789 RMVar_ID_52789 Human_SNP_ID_833717904 A-to-I Human chr19 + 49608510 49608510 49608510 CTCCTGCCTCAGCCTCCCGAGTAGCGCAGACTACAGGCAAGTGCCACCACACCCAGCTAATTTCT CTCCTGCCTCAGCCTCCCGAGTAGCGCAGACTGCAGGCAAGTGCCACCACACCCAGCTAATTTCT A G PRR12 Ensembl:ENSG00000126464 Protein coding intron GSE38233 cultured B-cells chr19:49608509..49608510 24183664 RNA-Seq:(High) rs117038286 Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_195887,RMVar_hsa_circ_115272,RMVar_hsa_circ_46183,RMVar_hsa_circ_368010 52790 RMVar_ID_52790 Human_SNP_ID_833718181 A-to-I Human chr19 + 48902683 48902683 48902683 TTGCCCGCCTCGGCCTCCCAAAGTGCTGGGATAATAGGTGTGAGCCACTGAGTTCTGAACTGGAG TTGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTATAGGTGTGAGCCACTGAGTTCTGAACTGGAG A T NUCB1 Ensembl:ENSG00000104805 Protein coding intron GSE100210 HepG2 cell line chr19:48902682..48902683 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 2 prostate Human_RBP_ID_6778289 RMVar_hsa_circ_195733,RMVar_hsa_circ_94007 52791 RMVar_ID_52791 Human_SNP_ID_833736278 A-to-I Human chr19 + 11006570 11006570 11006570 GTCAGGAGTTCGAGACCAGCCTGGCCAACATGATGAAACCCCGTCTCTACTAAAAAATACAAAAA GTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAAATACAAAAA A G SMARCA4 Ensembl:ENSG00000127616 Protein coding intron GSE38233 cultured B-cells chr19:11006569..11006570 24183664 RNA-Seq:(High) rs147318343 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Clinvar_Rec_92 GWAS_ID_2330,GWAS_ID_2331,GWAS_ID_2332,GWAS_ID_2333,GWAS_ID_2334,GWAS_ID_2335,GWAS_ID_2336,GWAS_ID_2337,GWAS_ID_2338,GWAS_ID_2339 RMVar_hsa_circ_2241,RMVar_hsa_circ_39568,RMVar_hsa_circ_51477,RMVar_hsa_circ_332540,RMVar_hsa_circ_7395,RMVar_hsa_circ_5044,RMVar_hsa_circ_75898,RMVar_hsa_circ_192482,RMVar_hsa_circ_21252,RMVar_hsa_circ_114765,RMVar_hsa_circ_192484 52792 RMVar_ID_52792 Human_SNP_ID_833772425 A-to-I Human chr19 + 14470208 14470208 14470208 GGACCGGACCAGCACATTCTGTGGGACCCCGGAGTTCCTGGCCCCTGAGGTGCTGACGGACACGT GGACCGGACCAGCACATTCTGTGGGACCCCGGCGTTCCTGGCCCCTGAGGTGCTGACGGACACGT A C PKN1 Ensembl:ENSG00000123143 Protein coding CDS GSE100210 HepG2 cell line chr19:14470207..14470208 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA 33..33 33 OV 1 - Human_RBP_ID_514372,Human_RBP_ID_8839171,Human_RBP_ID_9293468 Human_Splice_Rec_1968668,Human_Splice_Rec_1968669,Human_Splice_Rec_1968704,Human_Splice_Rec_1968705,Human_Splice_Rec_1968774,Human_Splice_Rec_1968775,Human_Splice_Rec_1968812,Human_Splice_Rec_1968813,Human_Splice_Rec_1968819 RMVar_hsa_circ_19581,RMVar_hsa_circ_266717 52793 RMVar_ID_52793 Human_SNP_ID_833790805 A-to-I Human chr19 + 34444746 34444746 34444746 GGAAGATGGCTTGAGCCCAAGAGGTAGAAGCTACAGTGAGCCGAGATCTTAACACTGCACTCCAG GGAAGATGGCTTGAGCCCAAGAGGTAGAAGCTGCAGTGAGCCGAGATCTTAACACTGCACTCCAG A G UBA2 Ensembl:ENSG00000126261 Protein coding intron GSE38233 cultured B-cells chr19:34444745..34444746 24183664 RNA-Seq:(High) rs1033012425 Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_6745021,Human_RBP_ID_8255970,Human_RBP_ID_13433423 RMVar_hsa_circ_9877,RMVar_hsa_circ_54140,RMVar_hsa_circ_125569,RMVar_hsa_circ_353894,RMVar_hsa_circ_291250,RMVar_hsa_circ_312685,RMVar_hsa_circ_276657,RMVar_hsa_circ_275866,RMVar_hsa_circ_21381,RMVar_hsa_circ_310937,RMVar_hsa_circ_194112,RMVar_hsa_circ_194113,RMVar_hsa_circ_194111,RMVar_hsa_circ_356926,RMVar_hsa_circ_288581,RMVar_hsa_circ_281045,RMVar_hsa_circ_273262,RMVar_hsa_circ_194121,RMVar_hsa_circ_119372,RMVar_hsa_circ_194123,RMVar_hsa_circ_194122,RMVar_hsa_circ_194119,RMVar_hsa_circ_194120,RMVar_hsa_circ_346878,RMVar_hsa_circ_368008,RMVar_hsa_circ_315612,RMVar_hsa_circ_301892,RMVar_hsa_circ_288271,RMVar_hsa_circ_104307,RMVar_hsa_circ_120108,RMVar_hsa_circ_28673,RMVar_hsa_circ_274934,RMVar_hsa_circ_194132,RMVar_hsa_circ_194133,RMVar_hsa_circ_194131,RMVar_hsa_circ_320255,RMVar_hsa_circ_279648,RMVar_hsa_circ_96875,RMVar_hsa_circ_76037,RMVar_hsa_circ_194136,RMVar_hsa_circ_194138,RMVar_hsa_circ_194137,RMVar_hsa_circ_317552,RMVar_hsa_circ_194134,RMVar_hsa_circ_194135,RMVar_hsa_circ_372722,RMVar_hsa_circ_376106,RMVar_hsa_circ_325763,RMVar_hsa_circ_274439,RMVar_hsa_circ_194143,RMVar_hsa_circ_194147,RMVar_hsa_circ_76308,RMVar_hsa_circ_77704,RMVar_hsa_circ_194145,RMVar_hsa_circ_194146,RMVar_hsa_circ_194144,RMVar_hsa_circ_194141,RMVar_hsa_circ_194142,RMVar_hsa_circ_278940,RMVar_hsa_circ_321941,RMVar_hsa_circ_368603,RMVar_hsa_circ_302325,RMVar_hsa_circ_105142,RMVar_hsa_circ_194150,RMVar_hsa_circ_194152,RMVar_hsa_circ_194153,RMVar_hsa_circ_194154,RMVar_hsa_circ_194151 52794 RMVar_ID_52794 Human_SNP_ID_833792846 A-to-I Human chr19 - 7252873 7252873 7252873 TTGACCTTGTGATCTGCCCGCCTTGGCCTCCCAGGGTGCTGGGATTACAGGCGTGAGCCACCGCG TTGACCTTGTGATCTGCCCGCCTTGGCCTCCCTGGGTGCTGGGATTACAGGCGTGAGCCACCGCG T A INSR Ensembl:ENSG00000171105 Protein coding intron GSE100210 HepG2 cell line chr19:7252872..7252873 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_3125,RMVar_hsa_circ_292925,RMVar_hsa_circ_191968,RMVar_hsa_circ_107734,RMVar_hsa_circ_351073,RMVar_hsa_circ_191967 52795 RMVar_ID_52795 Human_SNP_ID_833808519 A-to-I Human chr19 + 35575740 35575740 35575740 CAACTAGCCCTGAAAATGGATGGCACTGGAGCATCAGGCCCATACCCGGCCATCGCCAGCAGTCA CAACTAGCCCTGAAAATGGATGGCACTGGAGCGTCAGGCCCATACCCGGCCATCGCCAGCAGTCA A G AD000090.1 Ensembl:ENSG00000283907 lincRNA exon GSE100210 HepG2 cell line chr19:35575739..35575740 29129909 RNA-Seq:(High) rs62109966 Functional Loss SNV ICGC 33..33 33 LMS 1 - Human_RBP_ID_270101,Human_RBP_ID_1064019,Human_RBP_ID_4521098,Human_RBP_ID_5190631,Human_RBP_ID_5443005,Human_RBP_ID_5468659,Human_RBP_ID_5499419,Human_RBP_ID_6803196,Human_RBP_ID_8096729,Human_RBP_ID_8255988,Human_RBP_ID_8840581,Human_RBP_ID_9086863,Human_RBP_ID_9258621,Human_RBP_ID_9291857,Human_RBP_ID_13548737,Human_RBP_ID_17011164,Human_RBP_ID_17063375,Human_RBP_ID_17268045,Human_RBP_ID_17695346,Human_RBP_ID_17936269,Human_RBP_ID_18200692,Human_RBP_ID_18208633,Human_RBP_ID_18441102,Human_RBP_ID_18514858,Human_RBP_ID_20380048,Human_RBP_ID_21929851,Human_RBP_ID_22233974,Human_RBP_ID_22422486,Human_RBP_ID_22502420,Human_RBP_ID_22810494,Human_RBP_ID_23176346,Human_RBP_ID_23279576,Human_RBP_ID_23309543,Human_RBP_ID_23793567,Human_RBP_ID_26467462,Human_RBP_ID_26652666,Human_RBP_ID_26749474,Human_RBP_ID_26988693,Human_RBP_ID_27157562,Human_RBP_ID_27280890,Human_RBP_ID_27473449,Human_RBP_ID_27562410,Human_RBP_ID_27677532 52796 RMVar_ID_52796 Human_SNP_ID_833814170 A-to-I Human chr19 + 47201775 47201775 47201775 TCCACCTCAGCCTCCCGAGTATCTGGCATTACAGCTGCCCGCCACCACACCCGGCTAACTTTTGT TCCACCTCAGCCTCCCGAGTATCTGGCATTACGGCTGCCCGCCACCACACCCGGCTAACTTTTGT A G SAE1 Ensembl:ENSG00000142230 Protein coding intron GSE100210 HepG2 cell line chr19:47201774..47201775 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 5 breast RMVar_hsa_circ_44245,RMVar_hsa_circ_195562,RMVar_hsa_circ_118551,RMVar_hsa_circ_314514,RMVar_hsa_circ_195563 52797 RMVar_ID_52797 Human_SNP_ID_833814570 A-to-I Human chr19 + 47137267 47137267 47137267 AAAATTAGCCAGGTGTGGTGGTGGGTGCTTGTAATCCCAACTACTTGGGAGGCTGAGGCAGGAGA AAAATTAGCCAGGTGTGGTGGTGGGTGCTTGTCATCCCAACTACTTGGGAGGCTGAGGCAGGAGA A C SAE1 Ensembl:ENSG00000142230 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr19:47137266..47137267;chr19:47137267..47137268 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 52798 RMVar_ID_52798 Human_SNP_ID_833817229 A-to-I Human chr19 + 13773594 13773594 13773594 AAGGATGCAGTGTGCTTTGATTGCACTACTGCACTTCACCCTAAGCAACAGAGTGAGACCCCATC AAGGATGCAGTGTGCTTTGATTGCACTACTGCGCTTCACCCTAAGCAACAGAGTGAGACCCCATC A G MRI1 Ensembl:ENSG00000037757 Protein coding 3'UTR GSE47997;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line chr19:13773593..13773594 23474544,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1374307800 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue Human_RBP_ID_26464910 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 52799 RMVar_ID_52799 Human_SNP_ID_833834576 A-to-I Human chr19 - 38589217 38589217 38589217 CTCACTGCAACCTCCTCCTCCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGG CTCACTGCAACCTCCTCCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGG T C MAP4K1 Ensembl:ENSG00000104814 Protein coding intron GSE38233 cultured B-cells chr19:38589216..38589217 24183664 RNA-Seq:(High) rs1460487376 Functional Loss SNV COSMIC 33..33 33 oesophagus squamous_cell_carcinoma 4 oesophagus Human_RBP_ID_137430 Human_Splice_Rec_2003030,Human_Splice_Rec_2003031 RMVar_hsa_circ_110942,RMVar_hsa_circ_127237,RMVar_hsa_circ_119332,RMVar_hsa_circ_122070,RMVar_hsa_circ_113157,RMVar_hsa_circ_194594,RMVar_hsa_circ_194598,RMVar_hsa_circ_83164,RMVar_hsa_circ_108197,RMVar_hsa_circ_194600,RMVar_hsa_circ_76391,RMVar_hsa_circ_194599,RMVar_hsa_circ_194596,RMVar_hsa_circ_194597,RMVar_hsa_circ_194595,RMVar_hsa_circ_99244,RMVar_hsa_circ_194593,RMVar_hsa_circ_194601 52800 RMVar_ID_52800 Human_SNP_ID_833844468 A-to-I Human chr19 - 52031786 52031786 52031786 ACTGTGTTGGCCAGGCTGGCCTTGAACTCTCGACCCCGGGCGGTCCACCCGCCTCAGCCTCCCAA ACTGTGTTGGCCAGGCTGGCCTTGAACTCTCGCCCCCGGGCGGTCCACCCGCCTCAGCCTCCCAA T G ZNF432 Ensembl:ENSG00000256087 Protein coding 3'UTR GSE100210 HepG2 cell line chr19:52031785..52031786 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 52801 RMVar_ID_52801 Human_SNP_ID_833852744 A-to-I Human chr19 + 12950636 12950636 12950636 TGTTAGCCAGGATGGTCTCAATCTCCTGACCTAATGATCTGCCCGCCTTGGCCTCCCAAAGTGCT TGTTAGCCAGGATGGTCTCAATCTCCTGACCTGATGATCTGCCCGCCTTGGCCTCCCAAAGTGCT A G RAD23A Ensembl:ENSG00000179262 Protein coding intron GSE38233 cultured B-cells chr19:12950635..12950636;chr19:12950636..12950637 24183664 RNA-Seq:(High) rs2974753 Functional Loss SNV ICGC 33..33 33 ESCA 1 - 52802 RMVar_ID_52802 Human_SNP_ID_833854886 A-to-I Human chr19 - 11154356 11154356 11154356 GTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCTAGGCTGGTCTTAAACTCCCAGCCT GTTTGTATTTTTAGTAGAGATGGGGTTTCACCGTGTTGGCTAGGCTGGTCTTAAACTCCCAGCCT T C SPC24 Ensembl:ENSG00000161888 Protein coding intron GSE38233 cultured B-cells chr19:11154355..11154356 24183664 RNA-Seq:(High) rs143062905 Functional Loss SNV ICGC 33..33 33 LAML 1 - RMVar_hsa_circ_86595,RMVar_hsa_circ_192528 52803 RMVar_ID_52803 Human_SNP_ID_833858401 A-to-I Human chr19 - 38868522 38868522 38868522 TCAAACAAGCCCCCTGCCTCTGCCTACCAAGTAGCTGAGACTACAGGCACCTACCACCGTGCCTG TCAAACAAGCCCCCTGCCTCTGCCTACCAAGTGGCTGAGACTACAGGCACCTACCACCGTGCCTG T C RINL Ensembl:ENSG00000187994 Protein coding 3'UTR GSE38233;GSE107867 cultured B-cells;ASD brains,frontal_cortex chr19:38868521..38868522 24183664,30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 52804 RMVar_ID_52804 Human_SNP_ID_833859436 A-to-I Human chr19 - 38868430 38868430 38868430 TGAGGTCTCTCTTTGTTGCCCAGGCTGGTCTCAAACTCCTAACCTCAAGCAATCTGCCCACGTCG TGAGGTCTCTCTTTGTTGCCCAGGCTGGTCTCGAACTCCTAACCTCAAGCAATCTGCCCACGTCG T C RINL Ensembl:ENSG00000187994 Protein coding 3'UTR GSE38233 cultured B-cells chr19:38868429..38868430 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_26472469 52805 RMVar_ID_52805 Human_SNP_ID_833868916 A-to-I Human chr19 + 57217974 57217973 57217975 CCGCCACACCCAGCTAATTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGCTCAGGCTGG CCGCCACACCCAGCTAATTTTGTATTTTTAGT__AGACGGGGTTTCACCATGTTGCTCAGGCTGG TAG T ZNF264 Ensembl:ENSG00000083844 Protein coding 3'UTR GSE100210 HepG2 cell line chr19:57217973..57217974 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 33..34 33 PBCA 1 - RMVar_hsa_circ_196396,RMVar_hsa_circ_116332,RMVar_hsa_circ_196395 52806 RMVar_ID_52806 Human_SNP_ID_833878281 A-to-I Human chr19 + 44901434 44901434 44901434 TGTGCTGCCACCCTGTGGGCCTCCACATTACCAGGGAACACTTGTTAAAAGGTAGGTGGGGCCGG TGTGCTGCCACCCTGTGGGCCTCCACATTACCGGGGAACACTTGTTAAAAGGTAGGTGGGGCCGG A G TOMM40 Ensembl:ENSG00000130204 Protein coding intron GSE38233 cultured B-cells chr19:44901433..44901434 24183664 RNA-Seq:(High) rs405697 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 7 haematopoietic and lymphoid tissue Human_RBP_ID_26759711 Human_Splice_Rec_2017915 GWAS_ID_2763,GWAS_ID_2764,GWAS_ID_2765,GWAS_ID_2766,GWAS_ID_2767,GWAS_ID_2768,GWAS_ID_2769,GWAS_ID_2770 52807 RMVar_ID_52807 Human_SNP_ID_833881966 A-to-I Human chr19 - 35891804 35891804 35891804 GGATTGCAATGGTGTGATTTTGGCTCACTGCAACCTCTGCCTCCCGGGTTCAAGCTATTCCTGTG GGATTGCAATGGTGTGATTTTGGCTCACTGCAGCCTCTGCCTCCCGGGTTCAAGCTATTCCTGTG T C NFKBID Ensembl:ENSG00000167604 Protein coding intron GSE38233 cultured B-cells chr19:35891803..35891804 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 7 pancreas 52808 RMVar_ID_52808 Human_SNP_ID_833887606 A-to-I Human chr19 - 4820234 4820234 4820234 TTGTATTTTTAGTAGAGACGGGGTTTCACCATATTGGCCAGGCTGGTCTCGACCTCCTGATCTCG TTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGGTCTCGACCTCCTGATCTCG T C TICAM1 Ensembl:ENSG00000127666 Protein coding intron GSE100210 HepG2 cell line chr19:4820233..4820234 29129909 RNA-Seq:(High) rs1038909133 Functional Loss SNV ICGC 33..33 33 PRAD 1 - 52809 RMVar_ID_52809 Human_SNP_ID_833888430 A-to-I Human chr19 + 47732308 47732308 47732308 GCCCGGCTAATTTTTGTATTTTTAGTAGAGATAGCATTTCACCATGTTGTCCAGGCTGGTCTCTA GCCCGGCTAATTTTTGTATTTTTAGTAGAGATTGCATTTCACCATGTTGTCCAGGCTGGTCTCTA A T EHD2,AC010519.1 Ensembl:ENSG00000024422,Ensembl:ENSG00000268746 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line chr19:47732307..47732308 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 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 52810 RMVar_ID_52810 Human_SNP_ID_833894186 A-to-I Human chr19 - 6473938 6473938 6473938 CATCCATCTCCTCTTCCCAGAGTGCTGAAATTACAGGTGTGATCCACCGCGCCCGGCCTCCTGCA CATCCATCTCCTCTTCCCAGAGTGCTGAAATTGCAGGTGTGATCCACCGCGCCCGGCCTCCTGCA T C DENND1C Ensembl:ENSG00000205744 Protein coding intron GSE38233 cultured B-cells chr19:6473937..6473938 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_32138 52811 RMVar_ID_52811 Human_SNP_ID_833895741 A-to-I Human chr19 + 35575743 35575743 35575743 CTAGCCCTGAAAATGGATGGCACTGGAGCATCAGGCCCATACCCGGCCATCGCCAGCAGTCAATG CTAGCCCTGAAAATGGATGGCACTGGAGCATCGGGCCCATACCCGGCCATCGCCAGCAGTCAATG A G AD000090.1 Ensembl:ENSG00000283907 lincRNA exon GSE100210 HepG2 cell line chr19:35575742..35575743 29129909 RNA-Seq:(High) rs62109967 Functional Loss SNV ICGC 33..33 33 LMS 1 - Human_RBP_ID_270101,Human_RBP_ID_1064019,Human_RBP_ID_4521098,Human_RBP_ID_5190632,Human_RBP_ID_5443005,Human_RBP_ID_5468659,Human_RBP_ID_5499419,Human_RBP_ID_6803196,Human_RBP_ID_8096729,Human_RBP_ID_8255988,Human_RBP_ID_8840581,Human_RBP_ID_9086863,Human_RBP_ID_9258621,Human_RBP_ID_9291857,Human_RBP_ID_13548737,Human_RBP_ID_17011164,Human_RBP_ID_17063375,Human_RBP_ID_17268045,Human_RBP_ID_17695346,Human_RBP_ID_17936269,Human_RBP_ID_18200692,Human_RBP_ID_18208633,Human_RBP_ID_18441102,Human_RBP_ID_18514858,Human_RBP_ID_20380048,Human_RBP_ID_21929851,Human_RBP_ID_22233974,Human_RBP_ID_22422486,Human_RBP_ID_22502420,Human_RBP_ID_22810494,Human_RBP_ID_23176346,Human_RBP_ID_23279576,Human_RBP_ID_23309543,Human_RBP_ID_23793567,Human_RBP_ID_26474837,Human_RBP_ID_26652666,Human_RBP_ID_26749474,Human_RBP_ID_26988693,Human_RBP_ID_27157562,Human_RBP_ID_27280890,Human_RBP_ID_27473449,Human_RBP_ID_27562410,Human_RBP_ID_27677532 52812 RMVar_ID_52812 Human_SNP_ID_833896518 A-to-I Human chr19 + 49488915 49488915 49488915 TTTAGTAGAGACAGGGTTTCACCATATTGGCCAGGATGGTCTCGAACTCCTGACCTCAACTGATC TTTAGTAGAGACAGGGTTTCACCATATTGGCCTGGATGGTCTCGAACTCCTGACCTCAACTGATC A T RPL13A Ensembl:ENSG00000142541 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line chr19:49488914..49488915 23474544,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 3 breast Human_RBP_ID_13495489 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 52813 RMVar_ID_52813 Human_SNP_ID_833899527 A-to-I Human chr19 + 21118273 21118273 21118273 CAGGAGTTCAAGACCAGCCTGGCCAACATGGTAAAACCCCATCTCTACTAAAAATACAAAAATTT CAGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACAAAAATTT A G ZNF714 Ensembl:ENSG00000160352 Protein coding intron GSE56152 embryonic stem cells,wild type chr19:21118272..21118273 25708366 RNA-Seq:(High) rs757211062 Functional Loss SNV COSMIC 33..33 33 oesophagus squamous_cell_carcinoma 12 oesophagus Human_RBP_ID_138321 RMVar_hsa_circ_324022,RMVar_hsa_circ_304124,RMVar_hsa_circ_328507 52814 RMVar_ID_52814 Human_SNP_ID_833910638 A-to-I Human chr19 + 11656092 11656092 11656092 CAGCCTGACCAAGATGGAGAAACCCCATCTCTACTAAAAATACAAAAAAATTAGCCGGGCATGGT CAGCCTGACCAAGATGGAGAAACCCCATCTCTTCTAAAAATACAAAAAAATTAGCCGGGCATGGT A T AC008543.1 Ensembl:ENSG00000197332 lincRNA intron GSE38233 cultured B-cells chr19:11656091..11656092 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_36434 52815 RMVar_ID_52815 Human_SNP_ID_833918558 A-to-I Human chr19 - 16545871 16545871 16545871 ACGGTGGCTCATGCCTGTAATCCCTGCACTTTAGGAAGCCAGGGCAGGCAAATCAGTTGAGGTCA ACGGTGGCTCATGCCTGTAATCCCTGCACTTTGGGAAGCCAGGGCAGGCAAATCAGTTGAGGTCA T C AC008764.1 Ensembl:ENSG00000141979 Protein coding intron GSE100210 HepG2 cell line chr19:16545870..16545871 29129909 RNA-Seq:(High) rs1422267060 Functional Loss SNV ICGC 33..33 33 PRAD 1 - 52816 RMVar_ID_52816 Human_SNP_ID_833919042 A-to-I Human chr19 + 5662092 5662092 5662092 TATTTTCAGTAGAGACGGGGTTTCACTGTGTTAGCCAGGATGGTCTCTATCTCCTGACCTCGTGA TATTTTCAGTAGAGACGGGGTTTCACTGTGTTCGCCAGGATGGTCTCTATCTCCTGACCTCGTGA A C SAFB Ensembl:ENSG00000160633 Protein coding intron GSE38233 cultured B-cells chr19:5662091..5662092 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 52817 RMVar_ID_52817 Human_SNP_ID_833943604 A-to-I Human chr19 - 4824785 4824785 4824785 GGGACTACAGGCACCCGCCACCACACGTGGCTAATTTTTCTATTTTTAGTAGAGACGGGATTTCG GGGACTACAGGCACCCGCCACCACACGTGGCTGATTTTTCTATTTTTAGTAGAGACGGGATTTCG T C TICAM1 Ensembl:ENSG00000127666 Protein coding intron GSE38233 cultured B-cells chr19:4824784..4824785 24183664 RNA-Seq:(High) rs185115030 Functional Loss SNV ICGC 33..33 33 PAAD 1 - 52818 RMVar_ID_52818 Human_SNP_ID_833947682 A-to-I Human chr19 - 13332182 13332182 13332182 TGGCCGGGCTGGTCTTGAACTCCTTGCCTCAAATGATCTGCACACCTTGGCCTCCCAAAATGCTG TGGCCGGGCTGGTCTTGAACTCCTTGCCTCAAGTGATCTGCACACCTTGGCCTCCCAAAATGCTG T C CACNA1A Ensembl:ENSG00000141837 Protein coding intron GSE107867 ASD brains,cerebellum chr19:13332181..13332182 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_100582,RMVar_hsa_circ_192883,RMVar_hsa_circ_106634,RMVar_hsa_circ_192886,RMVar_hsa_circ_6638,RMVar_hsa_circ_12455,RMVar_hsa_circ_89082,RMVar_hsa_circ_192896,RMVar_hsa_circ_332679,RMVar_hsa_circ_339181,RMVar_hsa_circ_192903,RMVar_hsa_circ_301557,RMVar_hsa_circ_192902 52819 RMVar_ID_52819 Human_SNP_ID_833952282 A-to-I Human chr19 - 44100869 44100869 44100869 TCCAGCATCACATCTCGATACAGCTTCCTCTGAGCAAGGTCCAGCAGCCCCAGCTCTTCCTCAGT TCCAGCATCACATCTCGATACAGCTTCCTCTGGGCAAGGTCCAGCAGCCCCAGCTCTTCCTCAGT T C - - Other Unknown GSE107867 ASD brains,cerebellum chr19:44100868..44100869 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 2 liver 52820 RMVar_ID_52820 Human_SNP_ID_834016096 A-to-I Human chr19 + 44991367 44991367 44991367 GGGTGCTCAGCATGCTCTACGGCTTCCTGCTGACCTTCGGTGAGCGGTCCGGCCGCCCCAGGAGA GGGTGCTCAGCATGCTCTACGGCTTCCTGCTGGCCTTCGGTGAGCGGTCCGGCCGCCCCAGGAGA A G CLPTM1 Ensembl:ENSG00000104853 Protein coding CDS GSE100210 HepG2 cell line chr19:44991366..44991367 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_Splice_Rec_2018101,Human_Splice_Rec_2018125,Human_Splice_Rec_2018151 52821 RMVar_ID_52821 Human_SNP_ID_834030932 A-to-I Human chr19 - 3540069 3540069 3540069 AAAAAAAAAAAAGAAAAGAGATGGGTCTCACTATGTTGCTCAGGCTGGTCTTGAACTCCTGGGCT AAAAAAAAAAAAGAAAAGAGATGGGTCTCACTTTGTTGCTCAGGCTGGTCTTGAACTCCTGGGCT T A MFSD12 Ensembl:ENSG00000161091 Protein coding intron GSE100210 HepG2 cell line chr19:3540068..3540069 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 52822 RMVar_ID_52822 Human_SNP_ID_834032883 A-to-I Human chr19 + 13772567 13772567 13772567 ATGTGGATAACAGGCCGGGCGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGC ATGTGGATAACAGGCCGGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGC A G MRI1 Ensembl:ENSG00000037757 Protein coding 3'UTR GSE47997;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line chr19:13772566..13772567 23474544,29129909,31158229,31158229,31158229 RNA-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 52823 RMVar_ID_52823 Human_SNP_ID_823460707 A-to-I Human chr15 - 65771669 65771669 65771669 TATTTTTTGGGGGTGGATTTCCTTCAGGTAGTATACATTCTTTTTCAAATGGAAGAGCTGGTTAT TATTTTTTGGGGGTGGATTTCCTTCAGGTAGTGTACATTCTTTTTCAAATGGAAGAGCTGGTTAT T C DENND4A,AC011939.1 Ensembl:ENSG00000174485,Ensembl:ENSG00000259924 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line chr15:65771668..65771669 29129909 RNA-Seq:(High) rs896113067 Functional Loss SNV ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 8 lung,haematopoietic and lymphoid tissue Human_RBP_ID_1511744,Human_RBP_ID_6450076,Human_RBP_ID_9058801,Human_RBP_ID_9256618,Human_RBP_ID_12559371,Human_RBP_ID_22388427 RMVar_hsa_circ_173263,RMVar_hsa_circ_109648 52824 RMVar_ID_52824 Human_SNP_ID_823470226 A-to-I Human chr15 + 75090811 75090811 75090811 GTGATCTCGACTGACTGCTGCCTCCGCCTCCCAGGTTCAAGTGATTCTCCTGCCACAGCCTCCTG GTGATCTCGACTGACTGCTGCCTCCGCCTCCCCGGTTCAAGTGATTCTCCTGCCACAGCCTCCTG A C PPCDC Ensembl:ENSG00000138621 Protein coding intron GSE100210 HepG2 cell line chr15:75090810..75090811 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 52825 RMVar_ID_52825 Human_SNP_ID_823485725 A-to-I Human chr15 - 70672903 70672903 70672903 TTTAGTAGAGACGGGGTTTCACTATGTTGGCCAAGCTGGTCTTGAACTCCTGACCTCAGGCAATC TTTAGTAGAGACGGGGTTTCACTATGTTGGCCGAGCTGGTCTTGAACTCCTGACCTCAGGCAATC T C UACA Ensembl:ENSG00000137831 Protein coding intron GSE47997 K562 cells&HepG2 cells chr15:70672902..70672903 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - RMVar_hsa_circ_128063,RMVar_hsa_circ_118467,RMVar_hsa_circ_12622,RMVar_hsa_circ_173496,RMVar_hsa_circ_173495 52826 RMVar_ID_52826 Human_SNP_ID_823560847 A-to-I Human chr15 + 65771618 65771618 65771618 TCTTTCCTCTTCTCTTTCATGTCCACTATGTCAATGCTGATGTTGTTGGCTATAACCAGCTCTTC TCTTTCCTCTTCTCTTTCATGTCCACTATGTCGATGCTGATGTTGTTGGCTATAACCAGCTCTTC A G RAB11A Ensembl:ENSG00000103769 Protein coding intron GSE100210 HepG2 cell line chr15:65771617..65771618 29129909 RNA-Seq:(High) rs929878432 Functional Loss SNV ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 8 lung,haematopoietic and lymphoid tissue 52827 RMVar_ID_52827 Human_SNP_ID_823578081 A-to-I Human chr15 + 57394014 57394014 57394014 GCCATGGCACGATCATGGTTCACTGCAGCCTCAGCCTCCTAGGCTCAAGCCATCCTCCCATCTCA GCCATGGCACGATCATGGTTCACTGCAGCCTCGGCCTCCTAGGCTCAAGCCATCCTCCCATCTCA A G CGNL1 Ensembl:ENSG00000128849 Protein coding intron GSE47997 K562 cells&HepG2 cells chr15:57394013..57394014 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_Splice_Rec_1606694,Human_Splice_Rec_1606695 RMVar_hsa_circ_80820,RMVar_hsa_circ_113671,RMVar_hsa_circ_172380,RMVar_hsa_circ_172381 52828 RMVar_ID_52828 Human_SNP_ID_823618878 A-to-I Human chr15 - 50888487 50888487 50888487 CCTTTTATCGGGCCAAGGTAGGAGGATAATTTAAAGCTGGGAGTTTGAGACCAACCTGGACAACA CCTTTTATCGGGCCAAGGTAGGAGGATAATTTTAAGCTGGGAGTTTGAGACCAACCTGGACAACA T A AC021752.1 Ensembl:ENSG00000273674 lincRNA intron GSE100210 HepG2 cell line chr15:50888486..50888487 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 52829 RMVar_ID_52829 Human_SNP_ID_823619473 A-to-I Human chr15 + 64526066 64526066 64526066 CCTGCCTAGGCCTCCCAAAGTGCCGGGATTACAAGCATGAGCTACCACGCTCAGCCCTGTTTTTT CCTGCCTAGGCCTCCCAAAGTGCCGGGATTACCAGCATGAGCTACCACGCTCAGCCCTGTTTTTT A C ZNF609 Ensembl:ENSG00000180357 Protein coding intron GSE100210 HepG2 cell line chr15:64526066..64526067 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 2 breast RMVar_hsa_circ_120107,RMVar_hsa_circ_173052 52830 RMVar_ID_52830 Human_SNP_ID_823622392 A-to-I Human chr15 - 43812107 43812107 43812107 CAGCTCACTGCAGCCTCCGCCTGCCAGGTTCAAGTGATTTTCCTGCCTCAGCCTCCCAAGTAGCT CAGCTCACTGCAGCCTCCGCCTGCCAGGTTCACGTGATTTTCCTGCCTCAGCCTCCCAAGTAGCT T G MFAP1 Ensembl:ENSG00000140259 Protein coding intron GSE100210 HepG2 cell line chr15:43812106..43812107 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - RMVar_hsa_circ_3164,RMVar_hsa_circ_267845,RMVar_hsa_circ_378570 52831 RMVar_ID_52831 Human_SNP_ID_823624997 A-to-I Human chr15 + 59461521 59461521 59461521 TATAGTATTTTTTGTAGAGACATCGTCTCACTATGTTGCCCAGACAGGGCTTGAACTCCTGGGCT TATAGTATTTTTTGTAGAGACATCGTCTCACTGTGTTGCCCAGACAGGGCTTGAACTCCTGGGCT A G FAM81A Ensembl:ENSG00000157470 Protein coding intron GSE100210 HepG2 cell line chr15:59461520..59461521 29129909 RNA-Seq:(High) rs1189230581 Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_9376,RMVar_hsa_circ_172530,RMVar_hsa_circ_313753 52832 RMVar_ID_52832 Human_SNP_ID_823636322 A-to-I Human chr15 - 89897936 89897936 89897936 GCGCCACCACGACTAGCTAATTTTGTACTTTTAGTAGAGATGCGATTTCACCATGTTGGCTAGGC GCGCCACCACGACTAGCTAATTTTGTACTTTTTGTAGAGATGCGATTTCACCATGTTGGCTAGGC T A ARPIN,ARPIN-AP3S2 Ensembl:ENSG00000242498,Ensembl:ENSG00000250021 Protein coding,Protein coding 3'UTR,intron GSE100210;GSE112787;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831 HepG2 cell line;293 Flip-In T-REx cells,empty vector;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line chr15:89897935..89897936 29129909,29967493,31158229,31158229,31158229,32596459 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_12634291 RMVar_hsa_circ_347469,RMVar_hsa_circ_56287 52833 RMVar_ID_52833 Human_SNP_ID_823662848 A-to-I Human chr15 - 101283720 101283720 101283720 AGGATGGTCTCAATCTCTTGACCCCGTGATCCACCTGCCTCGTCTTCCCAAAGTGCTGGGATTAC AGGATGGTCTCAATCTCTTGACCCCGTGATCCGCCTGCCTCGTCTTCCCAAAGTGCTGGGATTAC T C SNRPA1 Ensembl:ENSG00000131876 Protein coding intron GSE100210 HepG2 cell line chr15:101283719..101283720 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 1 liver RMVar_hsa_circ_115260,RMVar_hsa_circ_109518,RMVar_hsa_circ_175225,RMVar_hsa_circ_175227,RMVar_hsa_circ_79442,RMVar_hsa_circ_175226 52834 RMVar_ID_52834 Human_SNP_ID_823693840 A-to-I Human chr15 - 51961226 51961226 51961226 GGCACCTGTCACCAAGCCCAGCTAGTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGG GGCACCTGTCACCAAGCCCAGCTAGTTTTTGTTTTTTTAGTAGAGACGGGGTTTCACCATGTTGG T A LEO1 Ensembl:ENSG00000166477 Protein coding intron GSE100210 HepG2 cell line chr15:51961225..51961226 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 3 prostate RMVar_hsa_circ_67985,RMVar_hsa_circ_8305,RMVar_hsa_circ_30577,RMVar_hsa_circ_74964,RMVar_hsa_circ_332272,RMVar_hsa_circ_172117 52835 RMVar_ID_52835 Human_SNP_ID_823716862 A-to-I Human chr15 - 41518447 41518447 41518447 GAATTCCTAATTTCGTGTGATCCGCCTGCCTCAGCCTCCCAAGTGCTGAGATTACAGGCGTGGCC GAATTCCTAATTTCGTGTGATCCGCCTGCCTCGGCCTCCCAAGTGCTGAGATTACAGGCGTGGCC T C RPAP1 Ensembl:ENSG00000103932 Protein coding intron GSE38233 cultured B-cells chr15:41518446..41518447 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_112881,RMVar_hsa_circ_117726,RMVar_hsa_circ_122638,RMVar_hsa_circ_116277,RMVar_hsa_circ_171082,RMVar_hsa_circ_80485,RMVar_hsa_circ_171083,RMVar_hsa_circ_171084,RMVar_hsa_circ_171080,RMVar_hsa_circ_171081 52836 RMVar_ID_52836 Human_SNP_ID_823720900 A-to-I Human chr15 + 44492189 44492189 44492189 TTGCGCCCGGCCAAAAAAAATTTTTTTAAATTAGCCGGGGATGGTGGCATGTGCCTGTAGTCCTA TTGCGCCCGGCCAAAAAAAATTTTTTTAAATTTGCCGGGGATGGTGGCATGTGCCTGTAGTCCTA A T CTDSPL2 Ensembl:ENSG00000137770 Protein coding intron GSE100210 HepG2 cell line chr15:44492188..44492189 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_4893,Human_RBP_ID_17563187 RMVar_hsa_circ_1278,RMVar_hsa_circ_69757,RMVar_hsa_circ_354023,RMVar_hsa_circ_327814,RMVar_hsa_circ_35505,RMVar_hsa_circ_65780,RMVar_hsa_circ_171589,RMVar_hsa_circ_68277,RMVar_hsa_circ_286875,RMVar_hsa_circ_340111,RMVar_hsa_circ_363025,RMVar_hsa_circ_171591,RMVar_hsa_circ_361990,RMVar_hsa_circ_90107,RMVar_hsa_circ_52061,RMVar_hsa_circ_97612,RMVar_hsa_circ_171595,RMVar_hsa_circ_295354,RMVar_hsa_circ_336422,RMVar_hsa_circ_282865,RMVar_hsa_circ_53651,RMVar_hsa_circ_171596,RMVar_hsa_circ_171598,RMVar_hsa_circ_171597 52837 RMVar_ID_52837 Human_SNP_ID_823731235 A-to-I Human chr15 - 89832556 89832556 89832556 TGAACCCGGGAGGCAGAGCTTGCAGTGAGCCAAGATCGCACCACTACACTCCAGCCTGGGCAACA TGAACCCGGGAGGCAGAGCTTGCAGTGAGCCAGGATCGCACCACTACACTCCAGCCTGGGCAACA T C AP3S2 Ensembl:ENSG00000157823 Protein coding 3'UTR GSE100210 HepG2 cell line chr15:89832555..89832556 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 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 52838 RMVar_ID_52838 Human_SNP_ID_823741767 A-to-I Human chr15 - 84641973 84641973 84641973 AATTCAGGTCAAGCATGTGGCTCATGTCTGTAATCCCAGTACTTTGGGAGGCTGAGGTGGGAGGA AATTCAGGTCAAGCATGTGGCTCATGTCTGTAGTCCCAGTACTTTGGGAGGCTGAGGTGGGAGGA T C WDR73 Ensembl:ENSG00000177082 Protein coding 3'UTR GSE100210 HepG2 cell line chr15:84641972..84641973 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 RECA 1 - 52839 RMVar_ID_52839 Human_SNP_ID_823759067 A-to-I Human chr15 - 25399707 25399707 25399707 TTTTAAAGCCAGGCGCGGTGCTGTGTATCTGTAGTCCTAGCTACCCGAGAGGCTGAAGAAGGAGG TTTTAAAGCCAGGCGCGGTGCTGTGTATCTGTTGTCCTAGCTACCCGAGAGGCTGAAGAAGGAGG T A UBE3A Ensembl:ENSG00000114062 Protein coding intron GSE107867 ASD brains,frontal_cortex chr15:25399707..25399708 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_12833,RMVar_hsa_circ_100889,RMVar_hsa_circ_323788,RMVar_hsa_circ_306052,RMVar_hsa_circ_265812,RMVar_hsa_circ_170219,RMVar_hsa_circ_333532,RMVar_hsa_circ_170218,RMVar_hsa_circ_296693,RMVar_hsa_circ_286177,RMVar_hsa_circ_267863,RMVar_hsa_circ_80104,RMVar_hsa_circ_3592,RMVar_hsa_circ_170221,RMVar_hsa_circ_170220,RMVar_hsa_circ_170224,RMVar_hsa_circ_371981,RMVar_hsa_circ_359126,RMVar_hsa_circ_170228,RMVar_hsa_circ_369021,RMVar_hsa_circ_321870,RMVar_hsa_circ_293298,RMVar_hsa_circ_14194,RMVar_hsa_circ_300529,RMVar_hsa_circ_302472,RMVar_hsa_circ_366356,RMVar_hsa_circ_320320,RMVar_hsa_circ_334080,RMVar_hsa_circ_291022,RMVar_hsa_circ_170230,RMVar_hsa_circ_170231 52840 RMVar_ID_52840 Human_SNP_ID_823781906 A-to-I Human chr15 + 92894666 92894666 92894666 TAAAAAGAATACCAGGCCAGGTGCAGTGGCTCAGGCCTGTAGTCCCAGCACTTTGGGGAGGCTGA TAAAAAGAATACCAGGCCAGGTGCAGTGGCTCGGGCCTGTAGTCCCAGCACTTTGGGGAGGCTGA A G LINC01578,AC013394.1 Ensembl:ENSG00000272888,Ensembl:ENSG00000279765 lincRNA,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells chr15:92894665..92894666 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_17869500 RMVar_hsa_circ_326458,RMVar_hsa_circ_62518,RMVar_hsa_circ_77798,RMVar_hsa_circ_174982 52841 RMVar_ID_52841 Human_SNP_ID_823785149 A-to-I Human chr15 - 65505793 65505793 65505793 GGTGCACACCACCATGCCTGGCTAATTTTTGTATTTTCAGTAGAGACGGGGTTTCATCATGTCAC GGTGCACACCACCATGCCTGGCTAATTTTTGTGTTTTCAGTAGAGACGGGGTTTCATCATGTCAC T C DPP8 Ensembl:ENSG00000074603 Protein coding intron GSE38233 cultured B-cells chr15:65505792..65505793 24183664 RNA-Seq:(High) rs918797425 Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 5 prostate Human_RBP_ID_12556883 RMVar_hsa_circ_173141,RMVar_hsa_circ_336881,RMVar_hsa_circ_173140,RMVar_hsa_circ_331946,RMVar_hsa_circ_279543,RMVar_hsa_circ_173142,RMVar_hsa_circ_45117,RMVar_hsa_circ_364428,RMVar_hsa_circ_316014,RMVar_hsa_circ_282712,RMVar_hsa_circ_66108,RMVar_hsa_circ_173150,RMVar_hsa_circ_42800,RMVar_hsa_circ_26411,RMVar_hsa_circ_173161,RMVar_hsa_circ_805,RMVar_hsa_circ_285487,RMVar_hsa_circ_173163,RMVar_hsa_circ_358449,RMVar_hsa_circ_314344,RMVar_hsa_circ_173164,RMVar_hsa_circ_329550,RMVar_hsa_circ_54421,RMVar_hsa_circ_282720,RMVar_hsa_circ_173173,RMVar_hsa_circ_173171,RMVar_hsa_circ_298216,RMVar_hsa_circ_126780,RMVar_hsa_circ_173172,RMVar_hsa_circ_278237,RMVar_hsa_circ_59905,RMVar_hsa_circ_292792,RMVar_hsa_circ_173177,RMVar_hsa_circ_356719,RMVar_hsa_circ_298421,RMVar_hsa_circ_110309,RMVar_hsa_circ_173180,RMVar_hsa_circ_173181,RMVar_hsa_circ_2274,RMVar_hsa_circ_119735,RMVar_hsa_circ_173183,RMVar_hsa_circ_329167,RMVar_hsa_circ_282183,RMVar_hsa_circ_284324,RMVar_hsa_circ_173182,RMVar_hsa_circ_324699,RMVar_hsa_circ_275167,RMVar_hsa_circ_173189,RMVar_hsa_circ_173191,RMVar_hsa_circ_77240,RMVar_hsa_circ_173192,RMVar_hsa_circ_173190,RMVar_hsa_circ_173188,RMVar_hsa_circ_283525,RMVar_hsa_circ_173193 52842 RMVar_ID_52842 Human_SNP_ID_823813124 A-to-I Human chr15 - 40694207 40694207 40694207 CTCGTCTTTAGTAAAAAATACAAAAATTAGCCAGGTTTTGTGGCACATGCCTGTAATCCTAGCTA CTCGTCTTTAGTAAAAAATACAAAAATTAGCCGGGTTTTGTGGCACATGCCTGTAATCCTAGCTA T C RAD51-AS1 Ensembl:ENSG00000245849 lincRNA intron GSE100210 HepG2 cell line chr15:40694206..40694207 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 52843 RMVar_ID_52843 Human_SNP_ID_823845504 A-to-I Human chr15 - 41076239 41076239 41076239 CTCCTGCTTCAGCCTCCTAAGTAGCTGGGATTACAGGCGCCTGCCACCATGCCTGGCTAATTTTT CTCCTGCTTCAGCCTCCTAAGTAGCTGGGATTGCAGGCGCCTGCCACCATGCCTGGCTAATTTTT T C INO80 Ensembl:ENSG00000128908 Protein coding intron GSE38233 cultured B-cells chr15:41076238..41076239 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_92257,RMVar_hsa_circ_170978,RMVar_hsa_circ_15350,RMVar_hsa_circ_118564,RMVar_hsa_circ_170993,RMVar_hsa_circ_170988,RMVar_hsa_circ_340068,RMVar_hsa_circ_362379,RMVar_hsa_circ_337666,RMVar_hsa_circ_317916,RMVar_hsa_circ_336402,RMVar_hsa_circ_371833,RMVar_hsa_circ_71454,RMVar_hsa_circ_171002,RMVar_hsa_circ_171003,RMVar_hsa_circ_266111,RMVar_hsa_circ_333491,RMVar_hsa_circ_93473,RMVar_hsa_circ_171004,RMVar_hsa_circ_10948,RMVar_hsa_circ_70352,RMVar_hsa_circ_33455,RMVar_hsa_circ_326792,RMVar_hsa_circ_310959,RMVar_hsa_circ_46166,RMVar_hsa_circ_171011,RMVar_hsa_circ_171012,RMVar_hsa_circ_319185,RMVar_hsa_circ_115728,RMVar_hsa_circ_65314,RMVar_hsa_circ_299635,RMVar_hsa_circ_318821,RMVar_hsa_circ_331745,RMVar_hsa_circ_301825,RMVar_hsa_circ_271744,RMVar_hsa_circ_171020,RMVar_hsa_circ_171022,RMVar_hsa_circ_171024,RMVar_hsa_circ_171023,RMVar_hsa_circ_171021,RMVar_hsa_circ_28703,RMVar_hsa_circ_294282,RMVar_hsa_circ_369789,RMVar_hsa_circ_127897,RMVar_hsa_circ_171026,RMVar_hsa_circ_171027,RMVar_hsa_circ_171025,RMVar_hsa_circ_282540,RMVar_hsa_circ_54622,RMVar_hsa_circ_2069,RMVar_hsa_circ_59266,RMVar_hsa_circ_45288 52844 RMVar_ID_52844 Human_SNP_ID_823846470 A-to-I Human chr15 - 22999594 22999594 22999594 GAGTTTGAGGCCAGCCTGGGCAACATGGTGAAACCCGGTGTCTACCAAAAATACAAAATGTATCC GAGTTTGAGGCCAGCCTGGGCAACATGGTGAAGCCCGGTGTCTACCAAAAATACAAAATGTATCC T C TUBGCP5 Ensembl:ENSG00000275835 Protein coding intron GSE100210 HepG2 cell line chr15:22999593..22999594 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA 33..33 33 UCEC 1 - RMVar_hsa_circ_21584 52845 RMVar_ID_52845 Human_SNP_ID_823860173 A-to-I Human chr15 + 75353745 75353745 75353745 TCTCTGCCTGTTCCTCTGTCCCACAGGGGGCAAAGGCTACGGGTCAGAGAGCGGGGAGGAGGACT TCTCTGCCTGTTCCTCTGTCCCACAGGGGGCAGAGGCTACGGGTCAGAGAGCGGGGAGGAGGACT A G NEIL1 Ensembl:ENSG00000140398 Protein coding CDS GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line chr15:75353745..75353746 32596459 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma 18 haematopoietic and lymphoid tissue Human_Splice_Rec_1628030,Human_Splice_Rec_1628086,Human_Splice_Rec_1628104 52846 RMVar_ID_52846 Human_SNP_ID_823879159 A-to-I Human chr15 + 59375099 59375099 59375099 AGCCAGGCATTCAAGACCAGCCTGGGCATCATAGCAAGACTCTGTCTCTATCAACAAATTATAAT AGCCAGGCATTCAAGACCAGCCTGGGCATCATTGCAAGACTCTGTCTCTATCAACAAATTATAAT A T FAM81A Ensembl:ENSG00000157470 Protein coding intron GSE100210 HepG2 cell line chr15:59375098..59375099 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 52847 RMVar_ID_52847 Human_SNP_ID_823879231 A-to-I Human chr15 + 45597358 45597358 45597358 AAAGTCAGCCTGGCGTGGTGGTGTGCACCTGTAGTCATAGCTACTTGGGAGGCTGAGGCAGGGGA AAAGTCAGCCTGGCGTGGTGGTGTGCACCTGTTGTCATAGCTACTTGGGAGGCTGAGGCAGGGGA A T AC090527.3,BLOC1S6 Ensembl:ENSG00000260170,Ensembl:ENSG00000104164 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line chr15:45597357..45597358 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 11 breast 52848 RMVar_ID_52848 Human_SNP_ID_823881478 A-to-I Human chr15 + 89201496 89201496 89201496 CATTCCACACAGCTTCCATATCTGAAGTGTTTAGTGGAGCAAAAATTGTACCATAAACTTGTGTT CATTCCACACAGCTTCCATATCTGAAGTGTTTGGTGGAGCAAAAATTGTACCATAAACTTGTGTT A G ABHD2 Ensembl:ENSG00000140526 Protein coding 3'UTR GSE100210 HepG2 cell line chr15:89201495..89201496 29129909 RNA-Seq:(High) rs1330636807 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue RMVar_hsa_circ_267600 52849 RMVar_ID_52849 Human_SNP_ID_823893089 A-to-I Human chr15 + 74593133 74593133 74593133 GGCTTGACCAGGCCCACTGTCTCCCTGTCCCCAGCAGAAGACAGAGCAGAGGCCTCGGCTGCAGC GGCTTGACCAGGCCCACTGTCTCCCTGTCCCCGGCAGAAGACAGAGCAGAGGCCTCGGCTGCAGC A G ARID3B Ensembl:ENSG00000179361 Protein coding intron GSE105773 Glioblastoma cells,U87MG chr15:74593132..74593133 29724793 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_887848 RMVar_hsa_circ_173865,RMVar_hsa_circ_97246,RMVar_hsa_circ_3669,RMVar_hsa_circ_282189,RMVar_hsa_circ_173871 52850 RMVar_ID_52850 Human_SNP_ID_823900589 A-to-I Human chr15 - 99257695 99257695 99257695 CTTCTACTGTACCTTCCACATCAACTTCATCAACAGCTCTGACCGACCCGAAGGTCAGCAGGACG CTTCTACTGTACCTTCCACATCAACTTCATCATCAGCTCTGACCGACCCGAAGGTCAGCAGGACG T A - - Other Unknown GSE38233 cultured B-cells chr15:99257694..99257695 24183664 RNA-Seq:(High) rs878940719 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 10 haematopoietic and lymphoid tissue 52851 RMVar_ID_52851 Human_SNP_ID_823919172 A-to-I Human chr15 - 41915211 41915211 41915211 TGACAAAATGACAGTTTTTCTCTAGGCTAATAACTCAATGAGCAGAAAGGAAAGTCCTCCCTTTT TGACAAAATGACAGTTTTTCTCTAGGCTAATAGCTCAATGAGCAGAAAGGAAAGTCCTCCCTTTT T C EHD4 Ensembl:ENSG00000103966 Protein coding intron GSE47997 K562 cells&HepG2 cells chr15:41915210..41915211 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - RMVar_hsa_circ_37826,RMVar_hsa_circ_91169,RMVar_hsa_circ_171166 52852 RMVar_ID_52852 Human_SNP_ID_823952775 A-to-I Human chr15 - 42417919 42417919 42417919 TGGCATGGTTGCTCTCTGATATTTGGCGTTGTAGATCATTTAAAACAACACTTGCTGACCGACCA TGGCATGGTTGCTCTCTGATATTTGGCGTTGTGGATCATTTAAAACAACACTTGCTGACCGACCA T C ZNF106 Ensembl:ENSG00000103994 Protein coding CDS GSE100210 HepG2 cell line chr15:42417918..42417919 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_8416609,Human_RBP_ID_12508622,Human_RBP_ID_18662618 Human_Splice_Rec_1590558,Human_Splice_Rec_1590594,Human_Splice_Rec_1590624,Human_Splice_Rec_1590666,Human_Splice_Rec_1590706,Human_Splice_Rec_1590716 RMVar_hsa_circ_82168,RMVar_hsa_circ_109960,RMVar_hsa_circ_171208,RMVar_hsa_circ_171206,RMVar_hsa_circ_171207,RMVar_hsa_circ_333637 52853 RMVar_ID_52853 Human_SNP_ID_824002918 A-to-I Human chr15 + 40396608 40396608 40396608 GGTTGAGGCCGGGTGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGTGG GGTTGAGGCCGGGTGCGGTGGCTCACACCTGTCATCCCAGCACTTTGGGAGGCCAAGGTGGGTGG A C - - Other Unknown GSE100210 HepG2 cell line chr15:40396607..40396608 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 52854 RMVar_ID_52854 Human_SNP_ID_824033531 A-to-I Human chr15 - 76212313 76212313 76212313 TTTAATCCTTGGCTTATAAAGCACTTTCATGTATGTCACCCCATCAGTTGGGGAAAGAGTAGAAA TTTAATCCTTGGCTTATAAAGCACTTTCATGTGTGTCACCCCATCAGTTGGGGAAAGAGTAGAAA T C - - Other Unknown GSE100210 HepG2 cell line chr15:76212312..76212313 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 52855 RMVar_ID_52855 Human_SNP_ID_824039807 A-to-I Human chr15 - 74632913 74632913 74632913 TCTGCCCACTAGCCCTGTGGACCTGGTCATCAACTGCCTGGATTGCCCTGAGAACGTCTTCCTGC TCTGCCCACTAGCCCTGTGGACCTGGTCATCAGCTGCCTGGATTGCCCTGAGAACGTCTTCCTGC T C EDC3 Ensembl:ENSG00000179151 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector chr15:74632912..74632913 29967493 RNA-Seq:(High) - Functional Loss SNV TCGA 33..33 33 BLCA 1 - Human_RBP_ID_463500,Human_RBP_ID_1002010,Human_RBP_ID_4333282,Human_RBP_ID_5464232,Human_RBP_ID_6462941,Human_RBP_ID_8802146,Human_RBP_ID_9283316,Human_RBP_ID_9371770,Human_RBP_ID_12589519,Human_RBP_ID_18668118,Human_RBP_ID_22496762,Human_RBP_ID_27436900 Human_Splice_Rec_1626022,Human_Splice_Rec_1626038,Human_Splice_Rec_1626048,Human_Splice_Rec_1626066,Human_Splice_Rec_1626080,Human_Splice_Rec_1626082 52856 RMVar_ID_52856 Human_SNP_ID_824072359 A-to-I Human chr15 - 89201238 89201238 89201238 GGAGAAATGATGAAGCTATCAGAAGCAAATCAACACCTGAGAGATGAAGGTTTAAGGCTCAGAAA GGAGAAATGATGAAGCTATCAGAAGCAAATCAGCACCTGAGAGATGAAGGTTTAAGGCTCAGAAA T C AC124068.1 Ensembl:ENSG00000259948 Pseudogene exon GSE100210 HepG2 cell line chr15:89201237..89201238 29129909 RNA-Seq:(High) rs1221058526 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue Human_RBP_ID_5567821 Human_miRNA_ID_1839307 52857 RMVar_ID_52857 Human_SNP_ID_824080416 A-to-I Human chr15 + 85579296 85579296 85579296 GCTGCCTTCAGAGCTTGCCTGATTGTGGAGTAAAGGGCACGGAAGGCCTTTCGTCCTGTGGAAAC GCTGCCTTCAGAGCTTGCCTGATTGTGGAGTACAGGGCACGGAAGGCCTTTCGTCCTGTGGAAAC A C AKAP13 Ensembl:ENSG00000170776 Protein coding CDS GSE100210 HepG2 cell line chr15:85579296..85579297 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA 33..33 33 BRCA 1 - Human_RBP_ID_5523802,Human_RBP_ID_6476190,Human_RBP_ID_8802823,Human_RBP_ID_9371215,Human_RBP_ID_18670623 RMVar_hsa_circ_113907,RMVar_hsa_circ_97471,RMVar_hsa_circ_174515,RMVar_hsa_circ_174516,RMVar_hsa_circ_375212,RMVar_hsa_circ_356482,RMVar_hsa_circ_85010,RMVar_hsa_circ_103712,RMVar_hsa_circ_174520,RMVar_hsa_circ_174521,RMVar_hsa_circ_351089,RMVar_hsa_circ_352600,RMVar_hsa_circ_76422,RMVar_hsa_circ_174522,RMVar_hsa_circ_66943,RMVar_hsa_circ_50656,RMVar_hsa_circ_55870,RMVar_hsa_circ_174524,RMVar_hsa_circ_296216,RMVar_hsa_circ_174525,RMVar_hsa_circ_35283,RMVar_hsa_circ_327723 52858 RMVar_ID_52858 Human_SNP_ID_824174026 A-to-I Human chr15 - 84634410 84634410 84634410 GTTCAATGTCAGCAAACTAGGCTTTACCTTCTAGAAAAATTCGAAGTATACCTCCACTTACCTTG GTTCAATGTCAGCAAACTAGGCTTTACCTTCTGGAAAAATTCGAAGTATACCTCCACTTACCTTG T C lnc-WDR73-7 RNACentral:URS00009B5F64 lincRNA intron GSE100210 HepG2 cell line chr15:84634409..84634410 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 2 - 52859 RMVar_ID_52859 Human_SNP_ID_824175244 A-to-I Human chr15 - 72356546 72356546 72356546 CTGTAGTCACACCTGGATGTAACCAGCTTCCTACTTTGGAGTCAGTGGAGAATTGTAAGTACCAT CTGTAGTCACACCTGGATGTAACCAGCTTCCTCCTTTGGAGTCAGTGGAGAATTGTAAGTACCAT T G HEXA,AC009690.1 Ensembl:ENSG00000213614,Ensembl:ENSG00000260729 Protein coding,Protein coding CDS,CDS GSE112787 293 Flip-In T-REx cells,empty vector chr15:72356545..72356546 29967493 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 5 lung Human_RBP_ID_884367,Human_RBP_ID_1364063,Human_RBP_ID_1833561,Human_RBP_ID_2453365,Human_RBP_ID_3946545,Human_RBP_ID_17865933,Human_RBP_ID_18667572,Human_RBP_ID_18981633,Human_RBP_ID_19068508,Human_RBP_ID_22758896 Human_Splice_Rec_1622648,Human_Splice_Rec_1622649,Human_Splice_Rec_1622678,Human_Splice_Rec_1622679,Human_Splice_Rec_1622710,Human_Splice_Rec_1622711,Human_Splice_Rec_1622735,Human_Splice_Rec_1622762,Human_Splice_Rec_1622763,Human_Splice_Rec_1622781,Human_Splice_Rec_1622800,Human_Splice_Rec_1622801,Human_Splice_Rec_1622826,Human_Splice_Rec_1622827,Human_Splice_Rec_1622838,Human_Splice_Rec_1622839,Human_Splice_Rec_1622856,Human_Splice_Rec_1622857,Human_Splice_Rec_1622878,Human_Splice_Rec_1622879,Human_Splice_Rec_1622886,Human_Splice_Rec_1622887,Human_Splice_Rec_1622896,Human_Splice_Rec_1622897 RMVar_hsa_circ_173732,RMVar_hsa_circ_20561,RMVar_hsa_circ_279793,RMVar_hsa_circ_173724,RMVar_hsa_circ_122311,RMVar_hsa_circ_8508,RMVar_hsa_circ_173727,RMVar_hsa_circ_62198,RMVar_hsa_circ_289926,RMVar_hsa_circ_173730,RMVar_hsa_circ_173728,RMVar_hsa_circ_362805,RMVar_hsa_circ_112924,RMVar_hsa_circ_173731,RMVar_hsa_circ_364480,RMVar_hsa_circ_269604,RMVar_hsa_circ_327554,RMVar_hsa_circ_117457,RMVar_hsa_circ_173733 52860 RMVar_ID_52860 Human_SNP_ID_824202198 A-to-I Human chr15 - 74868823 74868823 74868823 TTCACAAGGCTTGGCCAGGCATGGTGGCTCACACCTATAATCTCAGCAATTTGGGAGGCCAAGGC TTCACAAGGCTTGGCCAGGCATGGTGGCTCACCCCTATAATCTCAGCAATTTGGGAGGCCAAGGC T G SCAMP2 Ensembl:ENSG00000140497 Protein coding intron GSE38233 cultured B-cells chr15:74868822..74868823 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma,CLLE 2 haematopoietic and lymphoid tissue RMVar_hsa_circ_118372,RMVar_hsa_circ_173902,RMVar_hsa_circ_111829,RMVar_hsa_circ_173904 52861 RMVar_ID_52861 Human_SNP_ID_824215531 A-to-I Human chr15 - 43876035 43876035 43876035 TCTGGGATGAGATTCAATGAAGTGGCCACACAATATAGTGAAGATAAAGCCAGGCAAGGGGGCGT TCTGGGATGAGATTCAATGAAGTGGCCACACAGTATAGTGAAGATAAAGCCAGGCAAGGGGGCGT T C FRMD5,PIN4P1 Ensembl:ENSG00000171877,Ensembl:ENSG00000227973 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line chr15:43876034..43876035 29129909 RNA-Seq:(High) rs878996051 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 haematopoietic and lymphoid tissue Human_miRNA_ID_1829088 RMVar_hsa_circ_80728,RMVar_hsa_circ_17566,RMVar_hsa_circ_171562 52862 RMVar_ID_52862 Human_SNP_ID_824232042 A-to-I Human chr15 - 101684086 101684086 101684086 GCTTCCAGCAGGACGATGCTCACATTTTTTGCACAGTGGAGCAGGTAAACAATAACACAGAGTGA GCTTCCAGCAGGACGATGCTCACATTTTTTGCGCAGTGGAGCAGGTAAACAATAACACAGAGTGA T C TARS3 Ensembl:ENSG00000185418 Protein coding CDS GSE99789 esophageal squamous carcinoma cells,EC109 chr15:101684085..101684086 29796672 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 oesophagus squamous_cell_carcinoma 2 oesophagus Human_Splice_Rec_1651879,Human_Splice_Rec_1651907,Human_Splice_Rec_1651941,Human_Splice_Rec_1651985 Human_miRNA_ID_516185,Human_miRNA_ID_520412,Human_miRNA_ID_2181290,Human_miRNA_ID_2183394,Human_miRNA_ID_2969290 RMVar_hsa_circ_50524,RMVar_hsa_circ_268013,RMVar_hsa_circ_333228,RMVar_hsa_circ_371522,RMVar_hsa_circ_315163,RMVar_hsa_circ_766,RMVar_hsa_circ_30966,RMVar_hsa_circ_175253,RMVar_hsa_circ_175254,RMVar_hsa_circ_323748,RMVar_hsa_circ_53466,RMVar_hsa_circ_69998,RMVar_hsa_circ_175256,RMVar_hsa_circ_306341,RMVar_hsa_circ_45908,RMVar_hsa_circ_175257,RMVar_hsa_circ_34530,RMVar_hsa_circ_306436,RMVar_hsa_circ_344750,RMVar_hsa_circ_175258 52863 RMVar_ID_52863 Human_SNP_ID_824232050 A-to-I Human chr15 - 101684086 101684086 101684086 GCTTCCAGCAGGACGATGCTCACATTTTTTGCACAGTGGAGCAGGTAAACAATAACACAGAGTGA GCTTCCAGCAGGACGATGCTCACATTTTTTGCTCAGTGGAGCAGGTAAACAATAACACAGAGTGA T A TARS3 Ensembl:ENSG00000185418 Protein coding CDS GSE99789 esophageal squamous carcinoma cells,EC109 chr15:101684085..101684086 29796672 RNA-Seq:(High) - Functional Loss SNV TCGA,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 3 liver Human_Splice_Rec_1651879,Human_Splice_Rec_1651907,Human_Splice_Rec_1651941,Human_Splice_Rec_1651985 Human_miRNA_ID_516185,Human_miRNA_ID_520412,Human_miRNA_ID_2181290,Human_miRNA_ID_2183394,Human_miRNA_ID_2969290 RMVar_hsa_circ_50524,RMVar_hsa_circ_268013,RMVar_hsa_circ_333228,RMVar_hsa_circ_371522,RMVar_hsa_circ_315163,RMVar_hsa_circ_766,RMVar_hsa_circ_30966,RMVar_hsa_circ_175253,RMVar_hsa_circ_175254,RMVar_hsa_circ_323748,RMVar_hsa_circ_53466,RMVar_hsa_circ_69998,RMVar_hsa_circ_175256,RMVar_hsa_circ_306341,RMVar_hsa_circ_45908,RMVar_hsa_circ_175257,RMVar_hsa_circ_34530,RMVar_hsa_circ_306436,RMVar_hsa_circ_344750,RMVar_hsa_circ_175258 52864 RMVar_ID_52864 Human_SNP_ID_824240118 A-to-I Human chr15 + 50366593 50366593 50366593 AATTTTTGTATTTTTAGTAGAGATGGGGTTTTACCATGTTGGCCAGGCTGGCCTCAAACTCTGGA AATTTTTGTATTTTTAGTAGAGATGGGGTTTTCCCATGTTGGCCAGGCTGGCCTCAAACTCTGGA A C GABPB1-AS1 Ensembl:ENSG00000244879 lincRNA intron GSE100210 HepG2 cell line chr15:50366592..50366593 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 52865 RMVar_ID_52865 Human_SNP_ID_824258906 A-to-I Human chr15 - 82892734 82892734 82892734 GAGCAAGCAGGCGGTCACCGTTTCCTACTTCTATGATGTCACAAGGAACAGCTATCGGATCATCA GAGCAAGCAGGCGGTCACCGTTTCCTACTTCTGTGATGTCACAAGGAACAGCTATCGGATCATCA T C HOMER2 Ensembl:ENSG00000103942 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector chr15:82892733..82892734 29967493 RNA-Seq:(High) rs759254280 Functional Loss SNV COSMIC 33..33 33 head_neck squamous_cell_carcinoma 2 head and neck Human_RBP_ID_465677 Human_Splice_Rec_1637227,Human_Splice_Rec_1637243,Human_Splice_Rec_1637271,Human_Splice_Rec_1637281 RMVar_hsa_circ_174362,RMVar_hsa_circ_174364,RMVar_hsa_circ_287971,RMVar_hsa_circ_366521 52866 RMVar_ID_52866 Human_SNP_ID_824275159 A-to-I Human chr15 - 58899827 58899827 58899827 ACACAGCTCATGAAGAGATGGAAGCTCATACGACTGTGAAAGAAGCTGAGGATGACAACATCTCG ACACAGCTCATGAAGAGATGGAAGCTCATACGCCTGTGAAAGAAGCTGAGGATGACAACATCTCG T G SLTM Ensembl:ENSG00000137776 Protein coding CDS GSE100210 HepG2 cell line chr15:58899826..58899827 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - Human_RBP_ID_9370972,Human_RBP_ID_12539344,Human_RBP_ID_22496434,Human_RBP_ID_22934568,Human_RBP_ID_23113773 Human_Splice_Rec_1608080,Human_Splice_Rec_1608110,Human_Splice_Rec_1608152 Human_miRNA_ID_2286179,Human_miRNA_ID_2289177 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 52867 RMVar_ID_52867 Human_SNP_ID_824315480 A-to-I Human chr15 - 22970954 22970954 22970954 CTCCTGCCTCAGCCTCTCTAGGAGCTGGGATTACAGGCCCCCGCCACCACACCCAGCTAATTTTT CTCCTGCCTCAGCCTCTCTAGGAGCTGGGATTGCAGGCCCCCGCCACCACACCCAGCTAATTTTT T C CYFIP1 Ensembl:ENSG00000273749 Protein coding intron GSE100210 HepG2 cell line chr15:22970953..22970954 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 52868 RMVar_ID_52868 Human_SNP_ID_824315709 A-to-I Human chr15 + 72134458 72134458 72134458 AAAATTAGCCAGGCATGGTGGTACGCACCTGCAGTCCTAGCTACTCTGGAGGCAGAAGCCAGAAA AAAATTAGCCAGGCATGGTGGTACGCACCTGCGGTCCTAGCTACTCTGGAGGCAGAAGCCAGAAA A G SENP8 Ensembl:ENSG00000166192 Protein coding intron GSE100210 HepG2 cell line chr15:72134457..72134458 29129909 RNA-Seq:(High) rs960082177 Functional Loss SNV ICGC 33..33 33 LICA 1 - 52869 RMVar_ID_52869 Human_SNP_ID_824318645 A-to-I Human chr15 - 65503751 65503751 65503751 AGGCATGATGGCAGGTGCCTGTAATCCTAGCTACTCGGGAGGCTGAGGTGGGAGAATCGATTGAA AGGCATGATGGCAGGTGCCTGTAATCCTAGCTGCTCGGGAGGCTGAGGTGGGAGAATCGATTGAA T C DPP8 Ensembl:ENSG00000074603 Protein coding intron GSE38233 cultured B-cells chr15:65503750..65503751 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_173141,RMVar_hsa_circ_336881,RMVar_hsa_circ_173140,RMVar_hsa_circ_331946,RMVar_hsa_circ_279543,RMVar_hsa_circ_173142,RMVar_hsa_circ_45117,RMVar_hsa_circ_364428,RMVar_hsa_circ_316014,RMVar_hsa_circ_282712,RMVar_hsa_circ_66108,RMVar_hsa_circ_173150,RMVar_hsa_circ_42800,RMVar_hsa_circ_26411,RMVar_hsa_circ_173161,RMVar_hsa_circ_805,RMVar_hsa_circ_285487,RMVar_hsa_circ_173163,RMVar_hsa_circ_358449,RMVar_hsa_circ_314344,RMVar_hsa_circ_173164,RMVar_hsa_circ_329550,RMVar_hsa_circ_54421,RMVar_hsa_circ_282720,RMVar_hsa_circ_173173,RMVar_hsa_circ_173171,RMVar_hsa_circ_298216,RMVar_hsa_circ_126780,RMVar_hsa_circ_173172,RMVar_hsa_circ_278237,RMVar_hsa_circ_59905,RMVar_hsa_circ_292792,RMVar_hsa_circ_173177,RMVar_hsa_circ_356719,RMVar_hsa_circ_298421,RMVar_hsa_circ_110309,RMVar_hsa_circ_173180,RMVar_hsa_circ_173181,RMVar_hsa_circ_2274,RMVar_hsa_circ_119735,RMVar_hsa_circ_173183,RMVar_hsa_circ_329167,RMVar_hsa_circ_282183,RMVar_hsa_circ_284324,RMVar_hsa_circ_173182,RMVar_hsa_circ_324699,RMVar_hsa_circ_275167,RMVar_hsa_circ_173189,RMVar_hsa_circ_173191,RMVar_hsa_circ_77240,RMVar_hsa_circ_173192,RMVar_hsa_circ_173190,RMVar_hsa_circ_173188,RMVar_hsa_circ_283525,RMVar_hsa_circ_173193 52870 RMVar_ID_52870 Human_SNP_ID_824333581 A-to-I Human chr15 - 34342477 34342477 34342477 TCACTGCAACCTCCGCCTCCTGGGCTCAAACAATCCTTCTGCCTCAGCCTCCCGAGTAGTTGGGA TCACTGCAACCTCCGCCTCCTGGGCTCAAACAGTCCTTCTGCCTCAGCCTCCCGAGTAGTTGGGA T C NOP10 Ensembl:ENSG00000182117 Protein coding intron GSE38233 cultured B-cells chr15:34342476..34342477 24183664 RNA-Seq:(High) rs1253967889 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_102468,RMVar_hsa_circ_170546 52871 RMVar_ID_52871 Human_SNP_ID_824394931 A-to-I Human chr15 - 41059124 41059124 41059124 GACCCCATCTCTACATAAAATAAAATAAAATAAAAAAATTAGCCGGGCATGGTGGTATATGCCTG GACCCCATCTCTACATAAAATAAAATAAAATACAAAAATTAGCCGGGCATGGTGGTATATGCCTG T G INO80 Ensembl:ENSG00000128908 Protein coding intron GSE100210 HepG2 cell line chr15:41059123..41059124 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - RMVar_hsa_circ_599,RMVar_hsa_circ_92257,RMVar_hsa_circ_170978,RMVar_hsa_circ_15350,RMVar_hsa_circ_170983,RMVar_hsa_circ_89339,RMVar_hsa_circ_96852,RMVar_hsa_circ_170986,RMVar_hsa_circ_118564,RMVar_hsa_circ_170993,RMVar_hsa_circ_170988,RMVar_hsa_circ_340068,RMVar_hsa_circ_354541,RMVar_hsa_circ_375539,RMVar_hsa_circ_362379,RMVar_hsa_circ_351258,RMVar_hsa_circ_337666,RMVar_hsa_circ_317916,RMVar_hsa_circ_170995,RMVar_hsa_circ_170994,RMVar_hsa_circ_60772,RMVar_hsa_circ_336402,RMVar_hsa_circ_371833,RMVar_hsa_circ_71454,RMVar_hsa_circ_171002,RMVar_hsa_circ_171003,RMVar_hsa_circ_265736,RMVar_hsa_circ_266111,RMVar_hsa_circ_333491,RMVar_hsa_circ_93473,RMVar_hsa_circ_348116,RMVar_hsa_circ_171004,RMVar_hsa_circ_10948,RMVar_hsa_circ_50094,RMVar_hsa_circ_70352,RMVar_hsa_circ_33455,RMVar_hsa_circ_326792,RMVar_hsa_circ_332302,RMVar_hsa_circ_310959,RMVar_hsa_circ_67698,RMVar_hsa_circ_46166,RMVar_hsa_circ_171011,RMVar_hsa_circ_16942,RMVar_hsa_circ_171012,RMVar_hsa_circ_171010,RMVar_hsa_circ_319185,RMVar_hsa_circ_378848,RMVar_hsa_circ_171014 52872 RMVar_ID_52872 Human_SNP_ID_824423505 A-to-I Human chr15 + 42569472 42569472 42569472 GGGACTATAGGCACGCGCCACCACGCCTGGCTAATTTTTGTATTTTCTGTAGAGACAGAGTTTTG GGGACTATAGGCACGCGCCACCACGCCTGGCTGATTTTTGTATTTTCTGTAGAGACAGAGTTTTG A G HAUS2 Ensembl:ENSG00000137814 Protein coding 3'UTR GSE38233 cultured B-cells chr15:42569471..42569472 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_12509445 52873 RMVar_ID_52873 Human_SNP_ID_824435662 A-to-I Human chr15 - 76230162 76230162 76230162 ACTTGATTTTTATTTATTTATTTATTTTTTTGAGACAAGAGTCTCGCTCTGTCACCCAGGCTGAA ACTTGATTTTTATTTATTTATTTATTTTTTTGGGACAAGAGTCTCGCTCTGTCACCCAGGCTGAA T C ETFA,AC027243.1 Ensembl:ENSG00000140374,Ensembl:ENSG00000196274 Protein coding,Other intron,exon GSE100210 HepG2 cell line chr15:76230161..76230162 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 5 pancreas Human_RBP_ID_6465447 RMVar_hsa_circ_118874,RMVar_hsa_circ_122278,RMVar_hsa_circ_174026,RMVar_hsa_circ_174027,RMVar_hsa_circ_174029,RMVar_hsa_circ_63661,RMVar_hsa_circ_288511,RMVar_hsa_circ_302991,RMVar_hsa_circ_363997,RMVar_hsa_circ_70593,RMVar_hsa_circ_11079,RMVar_hsa_circ_174028 52874 RMVar_ID_52874 Human_SNP_ID_824440624 A-to-I Human chr15 - 34136861 34136860 34136862 ACCACGCCCGGGTAATTTTTTTGTATTTTTTTAGTAGAGACGGGGTTTCACCGTGTTAGGCAGGA ACCACGCCCGGGTAATTTTTTTGTATTTTTT__GTAGAGACGGGGTTTCACCGTGTTAGGCAGGA CTA C - - Other Unknown GSE100210 HepG2 cell line chr15:34136860..34136861 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 32..33 33 SKCA 1 - 52875 RMVar_ID_52875 Human_SNP_ID_824458338 A-to-I Human chr15 - 64358746 64358746 64358746 TGGGGTTTCTCCATGTTGGCCAGGCTGGTCTCAAACTTCTGACCTCAGATGACCCACCCTCCTTG TGGGGTTTCTCCATGTTGGCCAGGCTGGTCTCTAACTTCTGACCTCAGATGACCCACCCTCCTTG T A AC087632.2 Ensembl:ENSG00000259316 Protein coding intron GSE100210 HepG2 cell line chr15:64358745..64358746 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 RECA 1 - Human_RBP_ID_17563228 52876 RMVar_ID_52876 Human_SNP_ID_824478035 A-to-I Human chr15 + 64584539 64584539 64584539 GCCAGGCTGGTCTCGAACTCGTGACCTCAAGTAATCCACCCACCCAGCCTCTCAAAGTGCTGGGA GCCAGGCTGGTCTCGAACTCGTGACCTCAAGTGATCCACCCACCCAGCCTCTCAAAGTGCTGGGA A G ZNF609 Ensembl:ENSG00000180357 Protein coding intron GSE100210 HepG2 cell line chr15:64584538..64584539 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - RMVar_hsa_circ_120107,RMVar_hsa_circ_173052 52877 RMVar_ID_52877 Human_SNP_ID_824492223 A-to-I Human chr15 - 91297029 91297029 91297029 GAAGGAGCGTGCGCCCAACGATCAGGCAGAAGAAGCGTGCGCCCAACGATCGGGCAGAAGGAGCG GAAGGAGCGTGCGCCCAACGATCAGGCAGAAGGAGCGTGCGCCCAACGATCGGGCAGAAGGAGCG T C lnc-VPS33B-6,lnc-VPS33B-6:2,lnc-VPS33B-6:3 RNACentral:URS00008B374E,RNACentral:URS00008C0FC7,RNACentral:URS00008BA4FD lincRNA,lincRNA,lincRNA exon,intron,intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr15:91297028..91297029 30559470 RNA-Seq:(High) rs760291557 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 52878 RMVar_ID_52878 Human_SNP_ID_824523683 A-to-I Human chr15 - 50658137 50658137 50658137 AGCCGGGCATGGTGGCAGGAGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAGTGGTG AGCCGGGCATGGTGGCAGGAGCCTGTAGTCCCCGCTACTTGGGAGGCTGAGGCAGGAGAGTGGTG T G TRPM7 Ensembl:ENSG00000092439 Protein coding intron GSE38233 cultured B-cells chr15:50658136..50658137 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_83020,RMVar_hsa_circ_70540,RMVar_hsa_circ_171943,RMVar_hsa_circ_27742,RMVar_hsa_circ_265078,RMVar_hsa_circ_171946,RMVar_hsa_circ_27680,RMVar_hsa_circ_62672,RMVar_hsa_circ_373085,RMVar_hsa_circ_171954,RMVar_hsa_circ_20406,RMVar_hsa_circ_171958,RMVar_hsa_circ_171964,RMVar_hsa_circ_326377,RMVar_hsa_circ_281506,RMVar_hsa_circ_171965,RMVar_hsa_circ_361508,RMVar_hsa_circ_171973,RMVar_hsa_circ_308370,RMVar_hsa_circ_171976,RMVar_hsa_circ_304702,RMVar_hsa_circ_171977,RMVar_hsa_circ_297854,RMVar_hsa_circ_86763,RMVar_hsa_circ_171978,RMVar_hsa_circ_171979,RMVar_hsa_circ_275658,RMVar_hsa_circ_171982,RMVar_hsa_circ_171983,RMVar_hsa_circ_306191,RMVar_hsa_circ_171984 52879 RMVar_ID_52879 Human_SNP_ID_824560377 A-to-I Human chr15 - 64973616 64973616 64973616 GGAGAAACCCTGTCTACTAAAAATACAAAATTAGCTGGGCAAGGTGGCACATGCCTATAATCCCA GGAGAAACCCTGTCTACTAAAAATACAAAATTTGCTGGGCAAGGTGGCACATGCCTATAATCCCA T A SPG21 Ensembl:ENSG00000090487 Protein coding intron GSE100210 HepG2 cell line chr15:64973615..64973616 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_60181,RMVar_hsa_circ_329676,RMVar_hsa_circ_337636,RMVar_hsa_circ_340055,RMVar_hsa_circ_300153,RMVar_hsa_circ_338386,RMVar_hsa_circ_290674 52880 RMVar_ID_52880 Human_SNP_ID_824567817 A-to-I Human chr15 - 58883951 58883951 58883951 GGGATTATAGGTGTGGGGTACCATGCCTGACTAATTTTTTGTATTTTTAGTAGAAACGGGGTTGC GGGATTATAGGTGTGGGGTACCATGCCTGACTGATTTTTTGTATTTTTAGTAGAAACGGGGTTGC T C SLTM Ensembl:ENSG00000137776 Protein coding intron GSE38233 cultured B-cells chr15:58883950..58883951 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 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 52881 RMVar_ID_52881 Human_SNP_ID_824568511 A-to-I Human chr15 + 42671249 42671249 42671249 CAACCTCCTGGGCTCAAGTGATTCTCCTGCCTAAGCCTCCTGCATAGCTGGGATTACAGGCATGC CAACCTCCTGGGCTCAAGTGATTCTCCTGCCTCAGCCTCCTGCATAGCTGGGATTACAGGCATGC A C STARD9 Ensembl:ENSG00000159433 Protein coding intron GSE47997 K562 cells&HepG2 cells chr15:42671248..42671249;chr15:42671249..42671250 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast metaplastic_carcinoma 2 breast 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 52882 RMVar_ID_52882 Human_SNP_ID_824589556 A-to-I Human chr15 + 78486706 78486706 78486706 GATTTTTTGGTTTTGAGACAGTGTCTTGCTCTATTGCCCACACTGGAGTGCAGTGGTGCAATCAC GATTTTTTGGTTTTGAGACAGTGTCTTGCTCTGTTGCCCACACTGGAGTGCAGTGGTGCAATCAC A G IREB2 Ensembl:ENSG00000136381 Protein coding intron GSE38233 cultured B-cells chr15:78486705..78486706 24183664 RNA-Seq:(High) rs113727781 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 2 liver Human_RBP_ID_17563295 RMVar_hsa_circ_372734,RMVar_hsa_circ_296978,RMVar_hsa_circ_49009,RMVar_hsa_circ_28501,RMVar_hsa_circ_174168,RMVar_hsa_circ_339588,RMVar_hsa_circ_53625,RMVar_hsa_circ_329470,RMVar_hsa_circ_304423,RMVar_hsa_circ_345142,RMVar_hsa_circ_174179,RMVar_hsa_circ_42985,RMVar_hsa_circ_336611,RMVar_hsa_circ_376678,RMVar_hsa_circ_301833,RMVar_hsa_circ_55473,RMVar_hsa_circ_174178,RMVar_hsa_circ_297025,RMVar_hsa_circ_10724,RMVar_hsa_circ_174185,RMVar_hsa_circ_305205,RMVar_hsa_circ_9020,RMVar_hsa_circ_358877,RMVar_hsa_circ_43118 52883 RMVar_ID_52883 Human_SNP_ID_824590341 A-to-I Human chr15 + 50944751 50944751 50944751 ACTTACAGAGAGTTCCAAGAAACTATGATCCTACCTTACATCCTTTTGAGGTCCCATGAGAATAT ACTTACAGAGAGTTCCAAGAAACTATGATCCTGCCTTACATCCTTTTGAGGTCCCATGAGAATAT A G AP4E1,DCAF13P3 Ensembl:ENSG00000081014,Ensembl:ENSG00000259378 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line chr15:50944750..50944751 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue Human_RBP_ID_3490194 RMVar_hsa_circ_340872,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_48840,RMVar_hsa_circ_85453,RMVar_hsa_circ_360028,RMVar_hsa_circ_172016,RMVar_hsa_circ_35121,RMVar_hsa_circ_51178,RMVar_hsa_circ_54033,RMVar_hsa_circ_332411,RMVar_hsa_circ_335899,RMVar_hsa_circ_311736,RMVar_hsa_circ_172017 52884 RMVar_ID_52884 Human_SNP_ID_824599583 A-to-I Human chr15 - 34232304 34232304 34232304 AGGATCATTTGAACCCAGGAGGCGGAGGTTGCAGTGAGCCAGGATTGCACCTCTGCACTCCAGCC AGGATCATTTGAACCCAGGAGGCGGAGGTTGCTGTGAGCCAGGATTGCACCTCTGCACTCCAGCC T A SLC12A6 Ensembl:ENSG00000140199 Protein coding 3'UTR GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line chr15:34232303..34232304 32596459 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 52885 RMVar_ID_52885 Human_SNP_ID_824631669 A-to-I Human chr15 - 88989952 88989952 88989952 AACATTACCCGAATGGAGTCTGCACTGCGTATAGCAAAAAAAAAAAATAGATGGACAGCAAACCA AACATTACCCGAATGGAGTCTGCACTGCGTATGGCAAAAAAAAAAAATAGATGGACAGCAAACCA T C AC107954.1 Ensembl:ENSG00000261549 Pseudogene exon GSE38233 cultured B-cells chr15:88989951..88989952 24183664 RNA-Seq:(High) rs1239049224 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_17689282,Human_RBP_ID_26438810 Human_miRNA_ID_1823012 52886 RMVar_ID_52886 Human_SNP_ID_824685774 A-to-I Human chr15 + 85387189 85387189 85387189 AAACCCCGTCTCTACTAAAAAATACAAAAAATAGCTGGGCGTGGTGGTGGGCGCCTGTAATCCCA AAACCCCGTCTCTACTAAAAAATACAAAAAATTGCTGGGCGTGGTGGTGGGCGCCTGTAATCCCA A T AKAP13 Ensembl:ENSG00000170776 Protein coding intron GSE100210 HepG2 cell line chr15:85387188..85387189 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - 52887 RMVar_ID_52887 Human_SNP_ID_824694931 A-to-I Human chr15 - 41163832 41163832 41163832 TAATTGCTTAGCTTCTCGATTCCTTGCTGTGAATGTTGCTTTGAGGTCATCCCGTTTCATTTTCA TAATTGCTTAGCTTCTCGATTCCTTGCTGTGAGTGTTGCTTTGAGGTCATCCCGTTTCATTTTCA T C lnc-EXD1-1 RNACentral:URS00008BD8C6 lincRNA intron GSE100210 HepG2 cell line chr15:41163831..41163832 29129909 RNA-Seq:(High) rs1408544419 Functional Loss SNV ICGC 33..33 33 LAML 1 - 52888 RMVar_ID_52888 Human_SNP_ID_824704067 A-to-I Human chr15 - 52118712 52118712 52118712 AGGCATGCACCACCACGCCCGGCTAATTTTGTATTTTTAGTAGAGACCAGGTTTCTCCATGTTGG AGGCATGCACCACCACGCCCGGCTAATTTTGTGTTTTTAGTAGAGACCAGGTTTCTCCATGTTGG T C GNB5 Ensembl:ENSG00000069966 Protein coding 3'UTR GSE100210 HepG2 cell line chr15:52118711..52118712 29129909 RNA-Seq:(High) rs900522706 Functional Loss SNV ICGC 33..33 33 LUSC 1 - 52889 RMVar_ID_52889 Human_SNP_ID_824708296 A-to-I Human chr15 + 85579295 85579295 85579295 AGCTGCCTTCAGAGCTTGCCTGATTGTGGAGTAAAGGGCACGGAAGGCCTTTCGTCCTGTGGAAA AGCTGCCTTCAGAGCTTGCCTGATTGTGGAGTGAAGGGCACGGAAGGCCTTTCGTCCTGTGGAAA A G AKAP13 Ensembl:ENSG00000170776 Protein coding CDS GSE100210 HepG2 cell line chr15:85579294..85579295 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA 33..33 33 BRCA 1 - Human_RBP_ID_4337870,Human_RBP_ID_5523802,Human_RBP_ID_6476190,Human_RBP_ID_8802823,Human_RBP_ID_9371215,Human_RBP_ID_18670623 RMVar_hsa_circ_113907,RMVar_hsa_circ_97471,RMVar_hsa_circ_174515,RMVar_hsa_circ_174516,RMVar_hsa_circ_375212,RMVar_hsa_circ_356482,RMVar_hsa_circ_85010,RMVar_hsa_circ_103712,RMVar_hsa_circ_174520,RMVar_hsa_circ_174521,RMVar_hsa_circ_351089,RMVar_hsa_circ_352600,RMVar_hsa_circ_76422,RMVar_hsa_circ_174522,RMVar_hsa_circ_66943,RMVar_hsa_circ_50656,RMVar_hsa_circ_55870,RMVar_hsa_circ_174524,RMVar_hsa_circ_296216,RMVar_hsa_circ_174525,RMVar_hsa_circ_35283,RMVar_hsa_circ_327723 52890 RMVar_ID_52890 Human_SNP_ID_824709869 A-to-I Human chr15 - 64366934 64366934 64366934 GACAGGCTCTCTGTCCCCGAGGCTGGAGTGCAATGGCACAGTCTCAGCTCACTTCAAGCTCCACC GACAGGCTCTCTGTCCCCGAGGCTGGAGTGCATTGGCACAGTCTCAGCTCACTTCAAGCTCCACC T A AC087632.2,PCLAF Ensembl:ENSG00000259316,Ensembl:ENSG00000166803 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr15:64366933..64366934 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 RECA 1 - Human_RBP_ID_759475,Human_RBP_ID_12552276 RMVar_hsa_circ_38666 52891 RMVar_ID_52891 Human_SNP_ID_824717998 A-to-I Human chr15 - 52613181 52613181 52613181 TTGTATTTTTAGTAGAGGCGGTGTTTTGTCATATTGGCCAGACTGGTCTTGAACTCCTGACCTCA TTGTATTTTTAGTAGAGGCGGTGTTTTGTCATGTTGGCCAGACTGGTCTTGAACTCCTGACCTCA T C FAM214A Ensembl:ENSG00000047346 Protein coding intron GSE100210 HepG2 cell line chr15:52613180..52613181 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_319013,RMVar_hsa_circ_360823,RMVar_hsa_circ_53566,RMVar_hsa_circ_78068,RMVar_hsa_circ_352678,RMVar_hsa_circ_361408,RMVar_hsa_circ_172191,RMVar_hsa_circ_322815,RMVar_hsa_circ_359572,RMVar_hsa_circ_56056,RMVar_hsa_circ_172195,RMVar_hsa_circ_366463,RMVar_hsa_circ_297080,RMVar_hsa_circ_363840,RMVar_hsa_circ_365035 52892 RMVar_ID_52892 Human_SNP_ID_824722332 A-to-I Human chr15 - 99258611 99258611 99258611 ATTGGTTTGATATCATTCATAAGTTCCCATTCACAGACAGTTTTTTCAACTTTTTTAGTCTTTGG ATTGGTTTGATATCATTCATAAGTTCCCATTCCCAGACAGTTTTTTCAACTTTTTTAGTCTTTGG T G - - Other Unknown GSE38233 cultured B-cells chr15:99258610..99258611 24183664 RNA-Seq:(High) rs879204740 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 10 haematopoietic and lymphoid tissue 52893 RMVar_ID_52893 Human_SNP_ID_824730937 A-to-I Human chr15 - 59186655 59186655 59186655 TTTGAACTCCTGGGCTCAAGCCATTCTCTCCCACCTCAGTCTGCAAGTAGCTAGTACTACAGGCA TTTGAACTCCTGGGCTCAAGCCATTCTCTCCCTCCTCAGTCTGCAAGTAGCTAGTACTACAGGCA T A MYO1E Ensembl:ENSG00000157483 Protein coding intron GSE100210 HepG2 cell line chr15:59186654..59186655 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 2 oesophagus RMVar_hsa_circ_172479,RMVar_hsa_circ_123105,RMVar_hsa_circ_127410,RMVar_hsa_circ_127264,RMVar_hsa_circ_122506,RMVar_hsa_circ_172483,RMVar_hsa_circ_105799,RMVar_hsa_circ_92316,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_102320,RMVar_hsa_circ_172488,RMVar_hsa_circ_172489,RMVar_hsa_circ_369909,RMVar_hsa_circ_353320,RMVar_hsa_circ_275935,RMVar_hsa_circ_81330,RMVar_hsa_circ_97205,RMVar_hsa_circ_43360,RMVar_hsa_circ_64845,RMVar_hsa_circ_103072,RMVar_hsa_circ_172491,RMVar_hsa_circ_172493,RMVar_hsa_circ_172494,RMVar_hsa_circ_172492,RMVar_hsa_circ_172490,RMVar_hsa_circ_95167,RMVar_hsa_circ_97210,RMVar_hsa_circ_93592,RMVar_hsa_circ_172498,RMVar_hsa_circ_172500,RMVar_hsa_circ_63849,RMVar_hsa_circ_172499,RMVar_hsa_circ_172497,RMVar_hsa_circ_58138,RMVar_hsa_circ_121884,RMVar_hsa_circ_269227,RMVar_hsa_circ_91359,RMVar_hsa_circ_172501,RMVar_hsa_circ_86231,RMVar_hsa_circ_74087,RMVar_hsa_circ_343427,RMVar_hsa_circ_172502,RMVar_hsa_circ_172503,RMVar_hsa_circ_352263,RMVar_hsa_circ_351796,RMVar_hsa_circ_110466,RMVar_hsa_circ_342297,RMVar_hsa_circ_81693,RMVar_hsa_circ_68913,RMVar_hsa_circ_90991,RMVar_hsa_circ_172505,RMVar_hsa_circ_172506,RMVar_hsa_circ_360775,RMVar_hsa_circ_323571,RMVar_hsa_circ_12931,RMVar_hsa_circ_266654,RMVar_hsa_circ_309475,RMVar_hsa_circ_172507,RMVar_hsa_circ_362278,RMVar_hsa_circ_273360,RMVar_hsa_circ_52199,RMVar_hsa_circ_172508 52894 RMVar_ID_52894 Human_SNP_ID_824770174 A-to-I Human chr15 - 43140913 43140913 43140913 TGGAACTGCTGCAAGCTTTCTTCCTGGTGGCAAATGACATCATGGATTCATCCCTCACCCACTGG TGGAACTGCTGCAAGCTTTCTTCCTGGTGGCAGATGACATCATGGATTCATCCCTCACCCACTGG T C AC068724.4 Ensembl:ENSG00000285080 lincRNA intron GSE107867 ASD brains,temporal_cortex chr15:43140912..43140913 30559470 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 7 large intestine Human_RBP_ID_5569973 52895 RMVar_ID_52895 Human_SNP_ID_824780358 A-to-I Human chr15 + 34104393 34104393 34104393 GGGAGGCCGACCTGGGTGGATCACCTGAGATCAGGAATTCAAGACCAGCCTGGCCAACATGGTGA GGGAGGCCGACCTGGGTGGATCACCTGAGATCGGGAATTCAAGACCAGCCTGGCCAACATGGTGA A G PGBD4 Ensembl:ENSG00000182405 Protein coding 3'UTR GSE100210 HepG2 cell line chr15:34104392..34104393 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue 52896 RMVar_ID_52896 Human_SNP_ID_824815486 A-to-I Human chr15 + 30485040 30485040 30485040 GCTGGAGTGTGGAGGCAAGATCTTGGCTCACTACAACTTCCGCCTCCTAGGTTCAAGCAATTCTC GCTGGAGTGTGGAGGCAAGATCTTGGCTCACTTCAACTTCCGCCTCCTAGGTTCAAGCAATTCTC A T AC127502.1 Ensembl:ENSG00000215302 Pseudogene intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line chr15:30485039..30485040 31158229 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 52897 RMVar_ID_52897 Human_SNP_ID_824821176 A-to-I Human chr15 - 65788854 65788853 65788855 AATTATTACTTTTTTTTTTTTTTTTTTTTTTTAAGACAAGTCCTGGCTCTGTCACCCAGGCTGGG AATTATTACTTTTTTTTTTTTTTTTTTTTTT__AGACAAGTCCTGGCTCTGTCACCCAGGCTGGG TTA T DENND4A Ensembl:ENSG00000174485 Protein coding intron GSE100210 HepG2 cell line chr15:65788853..65788854 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 32..33 33 SKCA 1 - RMVar_hsa_circ_173263,RMVar_hsa_circ_109648 52898 RMVar_ID_52898 Human_SNP_ID_824869869 A-to-I Human chr15 + 41352740 41352740 41352740 CACCACGCCCGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTGCCCAGGCTGG CACCACGCCCGGCTAATTTTTGTATTTTTAGTGGAGACAGGGTTTCACCATGTTGCCCAGGCTGG A G NUSAP1,AC087721.2 Ensembl:ENSG00000137804,Ensembl:ENSG00000285920 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells chr15:41352739..41352740 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_99120,RMVar_hsa_circ_66562,RMVar_hsa_circ_171049,RMVar_hsa_circ_68859,RMVar_hsa_circ_64721,RMVar_hsa_circ_58522,RMVar_hsa_circ_26884,RMVar_hsa_circ_303269,RMVar_hsa_circ_335592,RMVar_hsa_circ_36821,RMVar_hsa_circ_355511,RMVar_hsa_circ_55546,RMVar_hsa_circ_74842,RMVar_hsa_circ_171051 52899 RMVar_ID_52899 Human_SNP_ID_824896351 A-to-I Human chr15 - 64366963 64366963 64366963 CCACGACCAACTAATTTTTTTTTTTTTTAGACAGGCTCTCTGTCCCCGAGGCTGGAGTGCAATGG CCACGACCAACTAATTTTTTTTTTTTTTAGACGGGCTCTCTGTCCCCGAGGCTGGAGTGCAATGG T C AC087632.2,PCLAF Ensembl:ENSG00000259316,Ensembl:ENSG00000166803 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line chr15:64366962..64366963 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_759475,Human_RBP_ID_6447384,Human_RBP_ID_12552277 RMVar_hsa_circ_38666 52900 RMVar_ID_52900 Human_SNP_ID_824902437 A-to-I Human chr15 - 101706187 101706187 101706187 GGTCAGGAGTTTGAGACCAGCCTGGCCAACATAGTGAAACCCTGTCTCTACTAAAAATACAAAAA GGTCAGGAGTTTGAGACCAGCCTGGCCAACATGGTGAAACCCTGTCTCTACTAAAAATACAAAAA T C TARS3 Ensembl:ENSG00000185418 Protein coding intron GSE47997 K562 cells&HepG2 cells chr15:101706186..101706187 23474544 RNA-Seq:(High) rs1416911520 Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 2 prostate RMVar_hsa_circ_371522,RMVar_hsa_circ_766,RMVar_hsa_circ_30966,RMVar_hsa_circ_175253,RMVar_hsa_circ_45908,RMVar_hsa_circ_344750,RMVar_hsa_circ_98532,RMVar_hsa_circ_175260,RMVar_hsa_circ_303057,RMVar_hsa_circ_276639,RMVar_hsa_circ_126114,RMVar_hsa_circ_59605,RMVar_hsa_circ_175262,RMVar_hsa_circ_175263,RMVar_hsa_circ_175261,RMVar_hsa_circ_97113,RMVar_hsa_circ_175268,RMVar_hsa_circ_286156,RMVar_hsa_circ_175269 52901 RMVar_ID_52901 Human_SNP_ID_824904654 A-to-I Human chr15 + 72590968 72590968 72590968 AACAAGGCTGGGCATGGCGGCTTACACCTTGTAATCCCAGCACTTTAGGAGGCTGAGGCAGGTGG AACAAGGCTGGGCATGGCGGCTTACACCTTGTTATCCCAGCACTTTAGGAGGCTGAGGCAGGTGG A T ARIH1,AC100827.3 Ensembl:ENSG00000166233,Ensembl:ENSG00000260534 Protein coding,lincRNA 3'UTR,exon GSE100210 HepG2 cell line chr15:72590968..72590969 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 52902 RMVar_ID_52902 Human_SNP_ID_824917628 A-to-I Human chr15 + 45600580 45600580 45600580 CAATTGATAGGACCATGTAATTTTTCTTCTTTAGCCTGTTGATGTGGTAGATTACATTGATTGAA CAATTGATAGGACCATGTAATTTTTCTTCTTTTGCCTGTTGATGTGGTAGATTACATTGATTGAA A T AC090527.3,BLOC1S6 Ensembl:ENSG00000260170,Ensembl:ENSG00000104164 Protein coding,Protein coding intron,intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line chr15:45600579..45600580 24183664,29129909,31158229 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ER-PR-HER-positive_carcinoma,breast HER-positive_carcinoma 19 breast Human_RBP_ID_458188,Human_RBP_ID_12519176 52903 RMVar_ID_52903 Human_SNP_ID_824927867 A-to-I Human chr15 - 65787142 65787142 65787142 TTGTAATATTGTTTTGTAGATGAGAGATTTTTATTTTTGAAAAGTTTTAAAAATAAATAGCAAAA TTGTAATATTGTTTTGTAGATGAGAGATTTTTGTTTTTGAAAAGTTTTAAAAATAAATAGCAAAA T C DENND4A Ensembl:ENSG00000174485 Protein coding intron GSE100210 HepG2 cell line chr15:65787141..65787142 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 3 ovary Human_RBP_ID_6450224,Human_RBP_ID_17563246 RMVar_hsa_circ_173263,RMVar_hsa_circ_109648 52904 RMVar_ID_52904 Human_SNP_ID_824942331 A-to-I Human chr15 + 22857716 22857716 22857716 AAAATTACCTGGGCATGGTGGCGCCCGCCTGTAGTCCCAGCTACTCGGGAGGCCGAGGCAGGAGA AAAATTACCTGGGCATGGTGGCGCCCGCCTGTGGTCCCAGCTACTCGGGAGGCCGAGGCAGGAGA A G NIPA2 Ensembl:ENSG00000140157 Protein coding intron GSE100210 HepG2 cell line chr15:22857715..22857716 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LMS 1 - RMVar_hsa_circ_189,RMVar_hsa_circ_17764,RMVar_hsa_circ_20603,RMVar_hsa_circ_19158,RMVar_hsa_circ_330388,RMVar_hsa_circ_326767,RMVar_hsa_circ_361653,RMVar_hsa_circ_28898 52905 RMVar_ID_52905 Human_SNP_ID_824958311 A-to-I Human chr15 + 45676289 45676289 45676289 CAAGAGGCTGTATTTGAGAACCTGGACAAACCAGGAGAGACCCAAGTGATTTCAGTGAGTGGTGA CAAGAGGCTGTATTTGAGAACCTGGACAAACCTGGAGAGACCCAAGTGATTTCAGTGAGTGGTGA A T AC090527.3,SQOR Ensembl:ENSG00000260170,Ensembl:ENSG00000137767 Protein coding,Protein coding CDS,CDS GSE100210 HepG2 cell line chr15:45676288..45676289 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BLCA,bladder transitional_cell_carcinoma,urinary_tract transitional_cell_carcinoma 4 bladder,urinary tract Human_RBP_ID_19068124 Human_Splice_Rec_1597657,Human_Splice_Rec_1597687 Human_miRNA_ID_2479364 RMVar_hsa_circ_103953,RMVar_hsa_circ_171723,RMVar_hsa_circ_127194,RMVar_hsa_circ_304282,RMVar_hsa_circ_75369,RMVar_hsa_circ_362762,RMVar_hsa_circ_171724,RMVar_hsa_circ_355116,RMVar_hsa_circ_75327,RMVar_hsa_circ_171725,RMVar_hsa_circ_344736,RMVar_hsa_circ_54854 52906 RMVar_ID_52906 Human_SNP_ID_824963571 A-to-I Human chr15 - 42880447 42880447 42880447 AGGAGTTCAAGGATATAATGAGCTATGATTGCACCACTGCACTCCAACCTGGGTGACAGAGCAAG AGGAGTTCAAGGATATAATGAGCTATGATTGCTCCACTGCACTCCAACCTGGGTGACAGAGCAAG T A TTBK2 Ensembl:ENSG00000128881 Protein coding intron GSE100210 HepG2 cell line chr15:42880446..42880447 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_25138972 52907 RMVar_ID_52907 Human_SNP_ID_824983369 A-to-I Human chr15 - 82044493 82044493 82044493 CAGGAAGGAGGATGTGGCCATGGCTCGGAGGGAGATCATCTCTGCTGCCGAGCACTTCTCCATGA CAGGAAGGAGGATGTGGCCATGGCTCGGAGGGTGATCATCTCTGCTGCCGAGCACTTCTCCATGA T A MEX3B Ensembl:ENSG00000183496 Protein coding CDS GSE47997 K562 cells&HepG2 cells chr15:82044492..82044493 23474544 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma 2 haematopoietic and lymphoid tissue Human_RBP_ID_6471982,Human_RBP_ID_22047636,Human_RBP_ID_26438312 52908 RMVar_ID_52908 Human_SNP_ID_825013678 A-to-I Human chr15 + 99258487 99258487 99258487 TTTATGTATGGAGCAGCAAGACTGAAACTGTTAAGGAGCCATGAAGGAAGAAGCAGCAGCAAAAG TTTATGTATGGAGCAGCAAGACTGAAACTGTTGAGGAGCCATGAAGGAAGAAGCAGCAGCAAAAG A G HSP90B2P,LRRC28 Ensembl:ENSG00000259706,Ensembl:ENSG00000168904 Pseudogene,Protein coding exon,intron GSE38233 cultured B-cells chr15:99258486..99258487 24183664 RNA-Seq:(High) rs879142326 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 5 haematopoietic and lymphoid tissue Human_RBP_ID_3490221,Human_RBP_ID_5096311,Human_RBP_ID_5247007,Human_RBP_ID_5567762,Human_RBP_ID_8251376,Human_RBP_ID_17367738,Human_RBP_ID_17484737,Human_RBP_ID_22388407 Human_miRNA_ID_1839309 RMVar_hsa_circ_353891,RMVar_hsa_circ_369034,RMVar_hsa_circ_369035,RMVar_hsa_circ_357147,RMVar_hsa_circ_175142,RMVar_hsa_circ_349426 52909 RMVar_ID_52909 Human_SNP_ID_825048588 A-to-I Human chr15 - 71899739 71899739 71899739 ACAGGGAAAGTAAAAGGTACCAAGAACAAAGGAAAAAAATTATCCTTTTGCAATCAACATGTAGA ACAGGGAAAGTAAAAGGTACCAAGAACAAAGGGAAAAAATTATCCTTTTGCAATCAACATGTAGA T C MYO9A Ensembl:ENSG00000066933 Protein coding CDS GSE38233 cultured B-cells chr15:71899739..71899740 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 5 large intestine Human_Splice_Rec_1621161,Human_Splice_Rec_1621295,Human_Splice_Rec_1621375,Human_Splice_Rec_1621471,Human_Splice_Rec_1621521 RMVar_hsa_circ_45448,RMVar_hsa_circ_98023,RMVar_hsa_circ_50363,RMVar_hsa_circ_173579,RMVar_hsa_circ_331091,RMVar_hsa_circ_95039,RMVar_hsa_circ_173581,RMVar_hsa_circ_173580,RMVar_hsa_circ_173590,RMVar_hsa_circ_78954,RMVar_hsa_circ_3413,RMVar_hsa_circ_269595,RMVar_hsa_circ_124185,RMVar_hsa_circ_173595,RMVar_hsa_circ_173597,RMVar_hsa_circ_345025,RMVar_hsa_circ_59486,RMVar_hsa_circ_365208,RMVar_hsa_circ_369381,RMVar_hsa_circ_363126,RMVar_hsa_circ_322251,RMVar_hsa_circ_34890,RMVar_hsa_circ_50709,RMVar_hsa_circ_126402,RMVar_hsa_circ_173601,RMVar_hsa_circ_328194,RMVar_hsa_circ_343408,RMVar_hsa_circ_74045,RMVar_hsa_circ_59880,RMVar_hsa_circ_173605,RMVar_hsa_circ_173606,RMVar_hsa_circ_67417,RMVar_hsa_circ_173608,RMVar_hsa_circ_173612,RMVar_hsa_circ_274523,RMVar_hsa_circ_306484,RMVar_hsa_circ_301150,RMVar_hsa_circ_102510,RMVar_hsa_circ_173610,RMVar_hsa_circ_173611,RMVar_hsa_circ_327278,RMVar_hsa_circ_10522,RMVar_hsa_circ_92675,RMVar_hsa_circ_334051,RMVar_hsa_circ_173615,RMVar_hsa_circ_54416,RMVar_hsa_circ_24782 52910 RMVar_ID_52910 Human_SNP_ID_825108080 A-to-I Human chr15 + 72563088 72563088 72563088 TGCTGTCTTTTTTTGAGGCAGGGCCTCATTCTAACACCCAGGCTGGAGTGCAGCAGATGATCACA TGCTGTCTTTTTTTGAGGCAGGGCCTCATTCTCACACCCAGGCTGGAGTGCAGCAGATGATCACA A C ARIH1 Ensembl:ENSG00000166233 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr15:72563087..72563088 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BOCA 1 - RMVar_hsa_circ_22868,RMVar_hsa_circ_22124,RMVar_hsa_circ_307863,RMVar_hsa_circ_173736,RMVar_hsa_circ_309093,RMVar_hsa_circ_294931,RMVar_hsa_circ_279703,RMVar_hsa_circ_173745,RMVar_hsa_circ_173746,RMVar_hsa_circ_173747,RMVar_hsa_circ_173744,RMVar_hsa_circ_173749,RMVar_hsa_circ_286529,RMVar_hsa_circ_296808,RMVar_hsa_circ_355253,RMVar_hsa_circ_305775,RMVar_hsa_circ_271075,RMVar_hsa_circ_173751,RMVar_hsa_circ_173752,RMVar_hsa_circ_173750,RMVar_hsa_circ_318711,RMVar_hsa_circ_173748,RMVar_hsa_circ_331645,RMVar_hsa_circ_313963,RMVar_hsa_circ_122192,RMVar_hsa_circ_112514,RMVar_hsa_circ_173757,RMVar_hsa_circ_71624,RMVar_hsa_circ_75803,RMVar_hsa_circ_173759,RMVar_hsa_circ_173758,RMVar_hsa_circ_173755,RMVar_hsa_circ_173756,RMVar_hsa_circ_85737,RMVar_hsa_circ_330529,RMVar_hsa_circ_44872,RMVar_hsa_circ_173762,RMVar_hsa_circ_173763,RMVar_hsa_circ_302076,RMVar_hsa_circ_322142,RMVar_hsa_circ_173764 52911 RMVar_ID_52911 Human_SNP_ID_825125573 A-to-I Human chr15 + 99258212 99258212 99258212 CAACTTCTGAATTGATTGGCCAGTTTGGTGTCAGTTTCTATTCCATCTTCCTTGTAGCAGATAAG CAACTTCTGAATTGATTGGCCAGTTTGGTGTCGGTTTCTATTCCATCTTCCTTGTAGCAGATAAG A G HSP90B2P,LRRC28 Ensembl:ENSG00000259706,Ensembl:ENSG00000168904 Pseudogene,Protein coding exon,intron GSE47997 K562 cells&HepG2 cells chr15:99258211..99258212 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 5 haematopoietic and lymphoid tissue RMVar_hsa_circ_353891,RMVar_hsa_circ_369034,RMVar_hsa_circ_369035,RMVar_hsa_circ_357147,RMVar_hsa_circ_175142,RMVar_hsa_circ_349426 52912 RMVar_ID_52912 Human_SNP_ID_825127822 A-to-I Human chr15 - 55859580 55859580 55859580 CGATTCTCATGCCTCAGCCTCCTGAATAGCTGAGATTACAGGCGCACACCACCACGCCCAGCTAA CGATTCTCATGCCTCAGCCTCCTGAATAGCTGGGATTACAGGCGCACACCACCACGCCCAGCTAA T C NEDD4 Ensembl:ENSG00000069869 Protein coding intron GSE47997 K562 cells&HepG2 cells chr15:55859579..55859580 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_172282,RMVar_hsa_circ_3239,RMVar_hsa_circ_54003,RMVar_hsa_circ_52006,RMVar_hsa_circ_83413,RMVar_hsa_circ_36043,RMVar_hsa_circ_27292,RMVar_hsa_circ_268063,RMVar_hsa_circ_70143,RMVar_hsa_circ_172278,RMVar_hsa_circ_41261,RMVar_hsa_circ_116185,RMVar_hsa_circ_339908,RMVar_hsa_circ_50179,RMVar_hsa_circ_117735,RMVar_hsa_circ_62520,RMVar_hsa_circ_172283,RMVar_hsa_circ_172281 52913 RMVar_ID_52913 Human_SNP_ID_825142178 A-to-I Human chr15 - 34270379 34270379 34270379 TAATTTAAAAAATGAGCCAGGCACAATGGCACACGCCTGTAGTCCCAGCACTTTAGGAGGCTGAG TAATTTAAAAAATGAGCCAGGCACAATGGCACGCGCCTGTAGTCCCAGCACTTTAGGAGGCTGAG T C SLC12A6 Ensembl:ENSG00000140199 Protein coding intron GSE47997 K562 cells&HepG2 cells chr15:34270378..34270379 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_349344,RMVar_hsa_circ_45955 52914 RMVar_ID_52914 Human_SNP_ID_825155835 A-to-I Human chr15 - 50568757 50568757 50568757 TCACCCAGGCTGCTCTCGAATTCCTGGGCTCAAGTGATCCACCTGCGTCAGCCTCCCAAAGTGCT TCACCCAGGCTGCTCTCGAATTCCTGGGCTCAGGTGATCCACCTGCGTCAGCCTCCCAAAGTGCT T C TRPM7 Ensembl:ENSG00000092439 Protein coding intron GSE100210 HepG2 cell line chr15:50568756..50568757 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_171916 52915 RMVar_ID_52915 Human_SNP_ID_825196370 A-to-I Human chr15 - 50945757 50945757 50945757 TTTCTAGTTATAATCCTTAGCTGCTTTTTCTCATGATGTAAGCACACCAAATTTTTCAGAAGCAT TTTCTAGTTATAATCCTTAGCTGCTTTTTCTCGTGATGTAAGCACACCAAATTTTTCAGAAGCAT T C - - Other Unknown GSE100210 HepG2 cell line chr15:50945756..50945757 29129909 RNA-Seq:(High) rs878899009 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue 52916 RMVar_ID_52916 Human_SNP_ID_825209182 A-to-I Human chr15 + 89267790 89267790 89267790 TCTACCAAAAAATAGAAAAATTAGCCGGGCATAGTGGCACATGCCTGTAGTCCCAGCTACTCAGG TCTACCAAAAAATAGAAAAATTAGCCGGGCATCGTGGCACATGCCTGTAGTCCCAGCTACTCAGG A C FANCI Ensembl:ENSG00000140525 Protein coding intron GSE38233 cultured B-cells chr15:89267789..89267790 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_16476,RMVar_hsa_circ_56441,RMVar_hsa_circ_351176,RMVar_hsa_circ_349689,RMVar_hsa_circ_32252,RMVar_hsa_circ_44177,RMVar_hsa_circ_50617,RMVar_hsa_circ_33118,RMVar_hsa_circ_19539,RMVar_hsa_circ_17057,RMVar_hsa_circ_12328,RMVar_hsa_circ_68986,RMVar_hsa_circ_363315,RMVar_hsa_circ_174635,RMVar_hsa_circ_11881,RMVar_hsa_circ_366788,RMVar_hsa_circ_339324,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_38038,RMVar_hsa_circ_31865,RMVar_hsa_circ_64160,RMVar_hsa_circ_174638,RMVar_hsa_circ_43937,RMVar_hsa_circ_337839,RMVar_hsa_circ_174641,RMVar_hsa_circ_51242,RMVar_hsa_circ_118555,RMVar_hsa_circ_174642 52917 RMVar_ID_52917 Human_SNP_ID_825212124 A-to-I Human chr15 + 99259522 99259522 99259522 GCCATTAAGGACAAGATTGAAAAGGCTATGGTATCTCAGTGCCTGACAGAATCTCTGTGTGCTTT GCCATTAAGGACAAGATTGAAAAGGCTATGGTTTCTCAGTGCCTGACAGAATCTCTGTGTGCTTT A T HSP90B2P,LRRC28 Ensembl:ENSG00000259706,Ensembl:ENSG00000168904 Pseudogene,Protein coding exon,intron GSE100210 HepG2 cell line chr15:99259521..99259522 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_5567767 RMVar_hsa_circ_353891,RMVar_hsa_circ_369034,RMVar_hsa_circ_369035,RMVar_hsa_circ_357147,RMVar_hsa_circ_175142,RMVar_hsa_circ_349426 52918 RMVar_ID_52918 Human_SNP_ID_825230280 A-to-I Human chr15 - 84712048 84712048 84712048 TTTGTAGAGATGGAGTCTCGCTATTCTGCCCAAGCTGGTCTCAAATTCCTGGGCTCGAGTGATCC TTTGTAGAGATGGAGTCTCGCTATTCTGCCCACGCTGGTCTCAAATTCCTGGGCTCGAGTGATCC T G SEC11A Ensembl:ENSG00000140612 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr15:84712047..84712048 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_759594,Human_RBP_ID_9811731 RMVar_hsa_circ_174461,RMVar_hsa_circ_363353 52919 RMVar_ID_52919 Human_SNP_ID_825258585 A-to-I Human chr15 - 90087256 90087248 90087257 CCATAACAGACCTTTTTACTCCCAGGCACTATAAGACCGACTTCGACAAGAATAAGATCTGGTAT CCATAACAGACCTTTTTACTCCCAGGCACTA_________CTTCGACAAGAATAAGATCTGGTAT GTCGGTCTTA G IDH2 Ensembl:ENSG00000182054 Protein coding CDS GSE100210 HepG2 cell line chr15:90087255..90087256 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 32..40 33 LICA 1 - Human_RBP_ID_466796 Human_Splice_Rec_1643554,Human_Splice_Rec_1643570,Human_Splice_Rec_1643586,Human_Splice_Rec_1643604 RMVar_hsa_circ_174723,RMVar_hsa_circ_174722,RMVar_hsa_circ_265615,RMVar_hsa_circ_105361,RMVar_hsa_circ_174724,RMVar_hsa_circ_346285 52920 RMVar_ID_52920 Human_SNP_ID_825259052 A-to-I Human chr15 - 41311350 41311350 41311350 GGAATGCAGTGGCACAGTCTTGGGTCACTGCAACCCCCTCCTCCCGGGTTCAAGCGATTCTCCCA GGAATGCAGTGGCACAGTCTTGGGTCACTGCAGCCCCCTCCTCCCGGGTTCAAGCGATTCTCCCA T C OIP5 Ensembl:ENSG00000104147 Protein coding intron GSE38233 cultured B-cells chr15:41311349..41311350 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_104612,RMVar_hsa_circ_171048,RMVar_hsa_circ_95181,RMVar_hsa_circ_171047 52921 RMVar_ID_52921 Human_SNP_ID_825272879 A-to-I Human chr15 + 84611716 84611716 84611716 GTTGCCAAGATCGCGCCACTGCACTCCAGCCTAGGCGACAGAGCGAGACTGTCTCAAAAAACACA GTTGCCAAGATCGCGCCACTGCACTCCAGCCTGGGCGACAGAGCGAGACTGTCTCAAAAAACACA A G ZSCAN2 Ensembl:ENSG00000176371 Protein coding intron GSE100210 HepG2 cell line chr15:84611715..84611716 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 52922 RMVar_ID_52922 Human_SNP_ID_825343897 A-to-I Human chr15 - 90976948 90976948 90976948 TTTTTTATTATTAGTAGAGATGGGGTTTCGCCATGTTGGCCAGGTTGGTCTGGAACTGTCGACCT TTTTTTATTATTAGTAGAGATGGGGTTTCGCCGTGTTGGCCAGGTTGGTCTGGAACTGTCGACCT T C AC068831.8,PRC1 Ensembl:ENSG00000284946,Ensembl:ENSG00000198901 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line chr15:90976947..90976948 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - RMVar_hsa_circ_75163,RMVar_hsa_circ_49308,RMVar_hsa_circ_106428,RMVar_hsa_circ_114313,RMVar_hsa_circ_109536,RMVar_hsa_circ_90798,RMVar_hsa_circ_174908,RMVar_hsa_circ_174910,RMVar_hsa_circ_174911,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_30689,RMVar_hsa_circ_370843,RMVar_hsa_circ_174919,RMVar_hsa_circ_98695,RMVar_hsa_circ_4497,RMVar_hsa_circ_174920,RMVar_hsa_circ_62368,RMVar_hsa_circ_174921,RMVar_hsa_circ_81400,RMVar_hsa_circ_345530,RMVar_hsa_circ_367696 52923 RMVar_ID_52923 Human_SNP_ID_825345741 A-to-I Human chr15 + 92911676 92911676 92911676 AGAGACGCTTGAACCTGGGAGGCGGAAGTTGCAGTGAGCTCAGATCGCACCACTCCACTCTAGCC AGAGACGCTTGAACCTGGGAGGCGGAAGTTGCTGTGAGCTCAGATCGCACCACTCCACTCTAGCC A T CHD2,AC013394.1 Ensembl:ENSG00000173575,Ensembl:ENSG00000279765 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line chr15:92911675..92911676 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_232319,Human_RBP_ID_12661762 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_174986 52924 RMVar_ID_52924 Human_SNP_ID_825346549 A-to-I Human chr15 - 99257696 99257696 99257696 TCTTCTACTGTACCTTCCACATCAACTTCATCAACAGCTCTGACCGACCCGAAGGTCAGCAGGAC TCTTCTACTGTACCTTCCACATCAACTTCATCGACAGCTCTGACCGACCCGAAGGTCAGCAGGAC T C - - Other Unknown GSE38233 cultured B-cells chr15:99257695..99257696 24183664 RNA-Seq:(High) rs878933727 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 10 haematopoietic and lymphoid tissue 52925 RMVar_ID_52925 Human_SNP_ID_825352934 A-to-I Human chr15 + 85387514 85387514 85387514 TACCTGGCTAATTTTTTTATTTTTGTAGAGACAGAGTCTCTCTATGTTGCCCAGGCTGGCCTCAA TACCTGGCTAATTTTTTTATTTTTGTAGAGACGGAGTCTCTCTATGTTGCCCAGGCTGGCCTCAA A G AKAP13 Ensembl:ENSG00000170776 Protein coding intron GSE100210 HepG2 cell line chr15:85387513..85387514 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 RECA 1 - 52926 RMVar_ID_52926 Human_SNP_ID_825376699 A-to-I Human chr15 + 43749569 43749569 43749569 TAATCCCAGCAGTTTGGGAGGCCAAGGCAGGCAGATCACTTGAGATCAGGAGTTCAGACCAGCCT TAATCCCAGCAGTTTGGGAGGCCAAGGCAGGCCGATCACTTGAGATCAGGAGTTCAGACCAGCCT A C PDIA3 Ensembl:ENSG00000167004 Protein coding intron GSE38233 cultured B-cells chr15:43749568..43749569 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_171531,RMVar_hsa_circ_114800,RMVar_hsa_circ_124137,RMVar_hsa_circ_171532 52927 RMVar_ID_52927 Human_SNP_ID_825393765 A-to-I Human chr15 + 66856729 66856729 66856729 GTCAGGCTGGTGTCTAACTCTGGACCTCAGGTAATCTGCCCACCTCAGCCTCCCAAAGTGCTGAG GTCAGGCTGGTGTCTAACTCTGGACCTCAGGTTATCTGCCCACCTCAGCCTCCCAAAGTGCTGAG A T - - Other Unknown GSE100210 HepG2 cell line chr15:66856728..66856729 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - 52928 RMVar_ID_52928 Human_SNP_ID_825496366 A-to-I Human chr15 + 39592766 39592766 39592766 ACGATGGCATTCCTGATGACAAGGACAACTGCAGACTCGTGCCCAATCCCGACCAGAAGGACTCT ACGATGGCATTCCTGATGACAAGGACAACTGCGGACTCGTGCCCAATCCCGACCAGAAGGACTCT A G THBS1 Ensembl:ENSG00000137801 Protein coding CDS GSE100210 HepG2 cell line chr15:39592765..39592766 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue plasma_cell_myeloma 1 haematopoietic and lymphoid tissue Human_RBP_ID_887442,Human_RBP_ID_9370674,Human_RBP_ID_22439956,Human_RBP_ID_22759176,Human_RBP_ID_27434453 Human_Splice_Rec_1582961 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 52929 RMVar_ID_52929 Human_SNP_ID_825500650 A-to-I Human chr15 - 89201239 89201239 89201239 GGGAGAAATGATGAAGCTATCAGAAGCAAATCAACACCTGAGAGATGAAGGTTTAAGGCTCAGAA GGGAGAAATGATGAAGCTATCAGAAGCAAATCGACACCTGAGAGATGAAGGTTTAAGGCTCAGAA T C AC124068.1 Ensembl:ENSG00000259948 Pseudogene exon GSE100210 HepG2 cell line chr15:89201238..89201239 29129909 RNA-Seq:(High) rs919896047 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue Human_RBP_ID_5567821 Human_miRNA_ID_1839307 52930 RMVar_ID_52930 Human_SNP_ID_825502841 A-to-I Human chr15 - 41089026 41089026 41089026 GCCACCATGCCTGGCTAATTTTTTTTATTTTTAGTAGAGATGTGGTTTCATCATGTTGGCCAGGC GCCACCATGCCTGGCTAATTTTTTTTATTTTTGGTAGAGATGTGGTTTCATCATGTTGGCCAGGC T C INO80 Ensembl:ENSG00000128908 Protein coding intron GSE38233 cultured B-cells chr15:41089025..41089026 24183664 RNA-Seq:(High) rs953772701 Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 7 ovary Human_RBP_ID_12501375 RMVar_hsa_circ_13904,RMVar_hsa_circ_92257,RMVar_hsa_circ_170978,RMVar_hsa_circ_15350,RMVar_hsa_circ_170993,RMVar_hsa_circ_340068,RMVar_hsa_circ_317916,RMVar_hsa_circ_371833,RMVar_hsa_circ_171003,RMVar_hsa_circ_333491,RMVar_hsa_circ_10948,RMVar_hsa_circ_326792,RMVar_hsa_circ_46166,RMVar_hsa_circ_115728,RMVar_hsa_circ_318821,RMVar_hsa_circ_331745,RMVar_hsa_circ_171024,RMVar_hsa_circ_171023,RMVar_hsa_circ_127897,RMVar_hsa_circ_171025,RMVar_hsa_circ_127167,RMVar_hsa_circ_54622,RMVar_hsa_circ_2069,RMVar_hsa_circ_349691,RMVar_hsa_circ_329363,RMVar_hsa_circ_171031,RMVar_hsa_circ_171032,RMVar_hsa_circ_171033,RMVar_hsa_circ_350399,RMVar_hsa_circ_352416,RMVar_hsa_circ_292211,RMVar_hsa_circ_74237,RMVar_hsa_circ_55716 52931 RMVar_ID_52931 Human_SNP_ID_825512914 A-to-I Human chr15 + 44515861 44515860 44515861 TGCCGTTGCACTCCAGCCTGGGCAACAAGAGCAAAACTCCATCTCAAAAAAAAAGACTTTAATAG TGCCGTTGCACTCCAGCCTGGGCAACAAGAGC_AAACTCCATCTCAAAAAAAAAGACTTTAATAG CA C CTDSPL2 Ensembl:ENSG00000137770 Protein coding intron GSE38233 cultured B-cells chr15:44515860..44515861 24183664 RNA-Seq:(High) - Functional Loss DEL ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_1278,RMVar_hsa_circ_35505,RMVar_hsa_circ_27347,RMVar_hsa_circ_52061,RMVar_hsa_circ_97612,RMVar_hsa_circ_171598,RMVar_hsa_circ_16500,RMVar_hsa_circ_306118,RMVar_hsa_circ_327231,RMVar_hsa_circ_171602,RMVar_hsa_circ_329597,RMVar_hsa_circ_348059,RMVar_hsa_circ_171606 52932 RMVar_ID_52932 Human_SNP_ID_844038102 A-to-I Human chr22 + 18100098 18100098 18100098 CTCTTTCTATTTATTGTTATTATTTTTGAGATAGAGTTTCAATCTTGTTGCCCAGGCTGGAGTGC CTCTTTCTATTTATTGTTATTATTTTTGAGATGGAGTTTCAATCTTGTTGCCCAGGCTGGAGTGC A G PEX26 Ensembl:ENSG00000215193 Protein coding 3'UTR GSE38233 cultured B-cells chr22:18100097..18100098 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 52933 RMVar_ID_52933 Human_SNP_ID_844050779 A-to-I Human chr22 + 21678839 21678839 21678839 GCTTCGACCTTCCAGGACCAAGTGCTCCTTCCACCTCAGTCTCCCAAGTAGATGGGACCACAGGC GCTTCGACCTTCCAGGACCAAGTGCTCCTTCCCCCTCAGTCTCCCAAGTAGATGGGACCACAGGC A C PPIL2 Ensembl:ENSG00000100023 Protein coding intron GSE100210 HepG2 cell line chr22:21678838..21678839 29129909 RNA-Seq:(High) rs934034677 Functional Loss SNV ICGC 33..33 33 SKCA 1 - RMVar_hsa_circ_17004,RMVar_hsa_circ_267588 52934 RMVar_ID_52934 Human_SNP_ID_844067022 A-to-I Human chr22 - 41064298 41064298 41064298 CTTCATCTTGCCCTCATCCAGCACCCCAATGCAGACCAGCCGCCACAGCAGGGCATTGCCTTCGA CTTCATCTTGCCCTCATCCAGCACCCCAATGCGGACCAGCCGCCACAGCAGGGCATTGCCTTCGA T C L13705-009,L13304-001 RNACentral:URS00001E2917,RNACentral:URS000044B5AA misc_RNA,scRNA intron,intron GSE100210 HepG2 cell line chr22:41064297..41064298 29129909 RNA-Seq:(High) rs879101686 Functional Loss SNV ICGC 33..33 33 BRCA 1 - 52935 RMVar_ID_52935 Human_SNP_ID_844067233 A-to-I Human chr22 - 20725906 20725906 20725906 TCTCCCTGGCTTTTTTTTTTTTTTTAAGAGACAGGGTCTCGCTCTGTCACTCAGGCTAGAGTGCA TCTCCCTGGCTTTTTTTTTTTTTTTAAGAGACCGGGTCTCGCTCTGTCACTCAGGCTAGAGTGCA T G PI4KA Ensembl:ENSG00000241973 Protein coding intron GSE100210 HepG2 cell line chr22:20725905..20725906 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 UTCA,endometrium carcinosarcoma-malignant_mesodermal_mixed_tumour 3 uterus 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_80854,RMVar_hsa_circ_213067,RMVar_hsa_circ_83593,RMVar_hsa_circ_121378,RMVar_hsa_circ_31708,RMVar_hsa_circ_213068,RMVar_hsa_circ_213069 52936 RMVar_ID_52936 Human_SNP_ID_844071785 A-to-I Human chr22 + 35661201 35661201 35661201 CAACATGGCAAAACCCTGTCTCTACTATAAATACAAAAATTAGCCAGGTGTAGTGGCAGGGCACT CAACATGGCAAAACCCTGTCTCTACTATAAATCCAAAAATTAGCCAGGTGTAGTGGCAGGGCACT A C APOL6 Ensembl:ENSG00000221963 Protein coding 3'UTR GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,KYSE180 cell line chr22:35661200..35661201 24183664,31158229,32596459 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 2 oesophagus RMVar_hsa_circ_125359,RMVar_hsa_circ_214023 52937 RMVar_ID_52937 Human_SNP_ID_844075771 A-to-I Human chr22 + 39051116 39051116 39051116 AAAATTAGCCAGGCGTGGGGGTGTGCCCCTGTAGTCCCAGCTACTTGGGTGGCTTAGGCAGGAAA AAAATTAGCCAGGCGTGGGGGTGTGCCCCTGTGGTCCCAGCTACTTGGGTGGCTTAGGCAGGAAA A G APOBEC3F Ensembl:ENSG00000128394 Protein coding intron GSE38233 cultured B-cells chr22:39051115..39051116 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 2 pancreas RMVar_hsa_circ_102365,RMVar_hsa_circ_214382 52938 RMVar_ID_52938 Human_SNP_ID_844083630 A-to-I Human chr22 - 20462423 20462423 20462423 TTGAGTCCAGGAGTTTTAGACTTCGGTGAACTATGATCATGCCCCTGTACTGTAGCCTGGGCAAC TTGAGTCCAGGAGTTTTAGACTTCGGTGAACTGTGATCATGCCCCTGTACTGTAGCCTGGGCAAC T C KLHL22 Ensembl:ENSG00000099910 Protein coding intron GSE100210 HepG2 cell line chr22:20462422..20462423 29129909 RNA-Seq:(High) rs1329117169 Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 2 prostate RMVar_hsa_circ_213033,RMVar_hsa_circ_345877,RMVar_hsa_circ_12450,RMVar_hsa_circ_276817,RMVar_hsa_circ_46747,RMVar_hsa_circ_213037 52939 RMVar_ID_52939 Human_SNP_ID_844088302 A-to-I Human chr22 + 41836078 41836078 41836078 CATAGGTCCATTAGGTTTGATCCCAGTGGAAGAAGATTCCATTTCTCTGTCCTTCCAGAAGACCT CATAGGTCCATTAGGTTTGATCCCAGTGGAAGTAGATTCCATTTCTCTGTCCTTCCAGAAGACCT A T SREBF2 Ensembl:ENSG00000198911 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr22:41836078..41836079 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_122139,RMVar_hsa_circ_214730,RMVar_hsa_circ_85583,RMVar_hsa_circ_214729 52940 RMVar_ID_52940 Human_SNP_ID_844089477 A-to-I Human chr22 - 27901667 27901667 27901667 GTTGGCCAGGCTGGTCTCGAACTCCCAACCTCAGGTGATCCTCCCACCTTGACCTCTGGCAAAGT GTTGGCCAGGCTGGTCTCGAACTCCCAACCTCGGGTGATCCTCCCACCTTGACCTCTGGCAAAGT T C PITPNB Ensembl:ENSG00000180957 Protein coding intron GSE38233 cultured B-cells chr22:27901666..27901667 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_14431878,Human_RBP_ID_23940207 RMVar_hsa_circ_213500,RMVar_hsa_circ_110113,RMVar_hsa_circ_377179,RMVar_hsa_circ_213504,RMVar_hsa_circ_326922,RMVar_hsa_circ_69086,RMVar_hsa_circ_213506,RMVar_hsa_circ_213508,RMVar_hsa_circ_278571,RMVar_hsa_circ_213513,RMVar_hsa_circ_87014,RMVar_hsa_circ_213514 52941 RMVar_ID_52941 Human_SNP_ID_844090088 A-to-I Human chr22 + 44096795 44096795 44096795 CTGTCCTTGGGCACGTTTTATTGCAGCTGGCTATGACGCACAAGGTGGGGAGGGCGGGGGCTCGG CTGTCCTTGGGCACGTTTTATTGCAGCTGGCTGTGACGCACAAGGTGGGGAGGGCGGGGGCTCGG A G PARVB Ensembl:ENSG00000188677 Protein coding intron GSE38233 cultured B-cells chr22:44096794..44096795 24183664 RNA-Seq:(High) rs2299849 Functional Loss SNV COSMIC 33..33 33 frontal_lobe astrocytoma_Grade_III,central_nervous_system astrocytoma_Grade_III 4 brain GWAS_ID_205,GWAS_ID_206 RMVar_hsa_circ_16447,RMVar_hsa_circ_214940,RMVar_hsa_circ_308836,RMVar_hsa_circ_310547,RMVar_hsa_circ_354388,RMVar_hsa_circ_46473,RMVar_hsa_circ_214938,RMVar_hsa_circ_214939 52942 RMVar_ID_52942 Human_SNP_ID_844092303 A-to-I Human chr22 - 49909950 49909950 49909950 CCTCCTGCTGCTGCTGGCCTTGGGCAACCGAAAGGTTTCTGTAGTCAGAGCCCTTCGCCACGCCG CCTCCTGCTGCTGCTGGCCTTGGGCAACCGAATGGTTTCTGTAGTCAGAGCCCTTCGCCACGCCG T A ALG12 Ensembl:ENSG00000182858 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector chr22:49909949..49909950 29967493 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 2 oesophagus Human_RBP_ID_18792042,Human_RBP_ID_19009483 Human_Splice_Rec_2178137,Human_Splice_Rec_2178153 RMVar_hsa_circ_89757,RMVar_hsa_circ_52795,RMVar_hsa_circ_215193,RMVar_hsa_circ_301635,RMVar_hsa_circ_215195 52943 RMVar_ID_52943 Human_SNP_ID_844094494 A-to-I Human chr22 + 45335169 45335169 45335169 TTTGCCAGCTGGCTCCTTCAGCGAGTCCTCGCACCAAGCCTGGGAGGTAGAGGTGAGGGCAGCGA TTTGCCAGCTGGCTCCTTCAGCGAGTCCTCGCGCCAAGCCTGGGAGGTAGAGGTGAGGGCAGCGA A G FAM118A Ensembl:ENSG00000100376 Protein coding intron GSE38233 cultured B-cells chr22:45335168..45335169 24183664 RNA-Seq:(High) rs2350629 Functional Loss SNV COSMIC 33..33 33 frontal_lobe astrocytoma_Grade_III,central_nervous_system astrocytoma_Grade_III 2 brain Human_RBP_ID_22086649,Human_RBP_ID_22550841,Human_RBP_ID_22674444 Human_Splice_Rec_2175319 GWAS_ID_210,GWAS_ID_211,GWAS_ID_212,GWAS_ID_213,GWAS_ID_214 RMVar_hsa_circ_56853,RMVar_hsa_circ_68942,RMVar_hsa_circ_214978,RMVar_hsa_circ_93063,RMVar_hsa_circ_214979,RMVar_hsa_circ_347303 52944 RMVar_ID_52944 Human_SNP_ID_844095136 A-to-I Human chr22 - 46713688 46713688 46713688 TGTTTTCACATTGATTCATGTTGGTCGCACCCAGTAGTTTGCTTATTTCATGACTGAAGGATGCT TGTTTTCACATTGATTCATGTTGGTCGCACCCGGTAGTTTGCTTATTTCATGACTGAAGGATGCT T C CERK Ensembl:ENSG00000100422 Protein coding intron GSE38233 cultured B-cells chr22:46713687..46713688 24183664 RNA-Seq:(High) rs135703 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_14523914,Human_RBP_ID_17147649 GWAS_ID_222 RMVar_hsa_circ_18547,RMVar_hsa_circ_268955,RMVar_hsa_circ_25482,RMVar_hsa_circ_330381,RMVar_hsa_circ_719,RMVar_hsa_circ_127219,RMVar_hsa_circ_334074,RMVar_hsa_circ_344224,RMVar_hsa_circ_215144,RMVar_hsa_circ_215145 52945 RMVar_ID_52945 Human_SNP_ID_844107736 A-to-I Human chr22 - 40626795 40626795 40626795 AGTGGCACGATCGTAGCTCACTGTAACCTTGAACCCCTGGCCTCAAGCAGTTCTCCCGCCTTGAA AGTGGCACGATCGTAGCTCACTGTAACCTTGACCCCCTGGCCTCAAGCAGTTCTCCCGCCTTGAA T G MRTFA Ensembl:ENSG00000196588 Protein coding intron GSE100210 HepG2 cell line chr22:40626794..40626795 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_23955143 52946 RMVar_ID_52946 Human_SNP_ID_844156416 A-to-I Human chr22 + 20063113 20063113 20063113 GGGAGGTGGAAGTTGCAGTGAGCCAAGATCGTACCATTGCGCTCTAGTCTGGGCGACAAGAGTGA GGGAGGTGGAAGTTGCAGTGAGCCAAGATCGTGCCATTGCGCTCTAGTCTGGGCGACAAGAGTGA A G TANGO2 Ensembl:ENSG00000183597 Protein coding intron GSE100210 HepG2 cell line chr22:20063112..20063113 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - Human_RBP_ID_23015345 RMVar_hsa_circ_40633,RMVar_hsa_circ_122439,RMVar_hsa_circ_212989,RMVar_hsa_circ_212990 52947 RMVar_ID_52947 Human_SNP_ID_844166478 A-to-I Human chr22 + 45341071 45341071 45341071 GTGATCCACCCGCCTTGGCCTCCCAAAGTGCTAGGATTACAGGCATGAGCCACTGCGCCCAGCAA GTGATCCACCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGCGCCCAGCAA A G FAM118A Ensembl:ENSG00000100376 Protein coding 3'UTR GSE99789 esophageal squamous carcinoma cells,EC109 chr22:45341070..45341071 29796672 RNA-Seq:(High) rs941398673 Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 1 prostate RMVar_hsa_circ_93063,RMVar_hsa_circ_214979 52948 RMVar_ID_52948 Human_SNP_ID_844167056 A-to-I Human chr22 + 26495031 26495031 26495031 CAAAGAGCAAAGACAATGTCCGTTTTCATCTCAGCTTACAGCAACCTCCGCCTCCCGGGTTCAAG CAAAGAGCAAAGACAATGTCCGTTTTCATCTCGGCTTACAGCAACCTCCGCCTCCCGGGTTCAAG A G - - Other Unknown GSE100210 HepG2 cell line chr22:26495030..26495031 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 haematopoietic and lymphoid tissue 52949 RMVar_ID_52949 Human_SNP_ID_844178785 A-to-I Human chr22 - 19450739 19450739 19450739 AAAATAGTATCTTCTCTTCAAACCTAGGATGAAGCTGGAGGCAGATTCGTCGCTTTCTCTGGAGA AAAATAGTATCTTCTCTTCAAACCTAGGATGAGGCTGGAGGCAGATTCGTCGCTTTCTCTGGAGA T C UFD1 Ensembl:ENSG00000070010 Protein coding CDS GSE100210 HepG2 cell line chr22:19450738..19450739 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_780927,Human_RBP_ID_932449,Human_RBP_ID_14393755,Human_RBP_ID_22673893,Human_RBP_ID_23935247,Human_RBP_ID_24561083,Human_RBP_ID_25680553 Human_Splice_Rec_2137098,Human_Splice_Rec_2137140,Human_Splice_Rec_2137154 RMVar_hsa_circ_104711,RMVar_hsa_circ_212954 52950 RMVar_ID_52950 Human_SNP_ID_844184357 A-to-I Human chr22 - 31741870 31741870 31741870 AAAGGGATACATTTCTCTCAGCACTGTTTTTGAGACGGAGTCTCACTCTGTCACCCAGGCTGGAG AAAGGGATACATTTCTCTCAGCACTGTTTTTGGGACGGAGTCTCACTCTGTCACCCAGGCTGGAG T C PRR14L Ensembl:ENSG00000183530 Protein coding intron GSE38233 cultured B-cells chr22:31741869..31741870 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 2 liver 52951 RMVar_ID_52951 Human_SNP_ID_844216447 A-to-I Human chr22 - 20722236 20722236 20722236 GTTGCAGTGAGCTGAGATTGTACCACTGCACTACAGCCTGGGTGACAGACCGAGACTCTGTCTCA GTTGCAGTGAGCTGAGATTGTACCACTGCACTCCAGCCTGGGTGACAGACCGAGACTCTGTCTCA T G PI4KA Ensembl:ENSG00000241973 Protein coding intron GSE38233 cultured B-cells chr22:20722235..20722236 24183664 RNA-Seq:(High) rs1446757023 Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 1 prostate 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_80854,RMVar_hsa_circ_213067,RMVar_hsa_circ_83593,RMVar_hsa_circ_121378,RMVar_hsa_circ_31708,RMVar_hsa_circ_213068,RMVar_hsa_circ_213069 52952 RMVar_ID_52952 Human_SNP_ID_844216979 A-to-I Human chr22 + 29230804 29230804 29230804 CGAGACCTCGTCTCTACAAATAATTTTTTTTTAAATTTGCCATGTGTGGTGGTGCATCCCTGTGG CGAGACCTCGTCTCTACAAATAATTTTTTTTTTAATTTGCCATGTGTGGTGGTGCATCCCTGTGG A T EMID1 Ensembl:ENSG00000186998 Protein coding intron GSE38233 cultured B-cells chr22:29230803..29230804 24183664 RNA-Seq:(High) rs3765295 Functional Loss SNV ICGC 33..33 33 COCA 1 - 52953 RMVar_ID_52953 Human_SNP_ID_844218919 A-to-I Human chr22 - 41466284 41466284 41466284 AACTCTGAGCCAAATGCCAGGAGAGAGAGCTTATAGACTAGTGCTACAGGCAAGATTTACCCCAT AACTCTGAGCCAAATGCCAGGAGAGAGAGCTTGTAGACTAGTGCTACAGGCAAGATTTACCCCAT T C PHF5A Ensembl:ENSG00000100410 Protein coding intron GSE38233 cultured B-cells chr22:41466283..41466284 24183664 RNA-Seq:(High) rs5758368 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_14506163 GWAS_ID_200,GWAS_ID_201,GWAS_ID_202,GWAS_ID_203,GWAS_ID_204 RMVar_hsa_circ_75997,RMVar_hsa_circ_98699,RMVar_hsa_circ_88245,RMVar_hsa_circ_214663,RMVar_hsa_circ_214664,RMVar_hsa_circ_214662 52954 RMVar_ID_52954 Human_SNP_ID_844228172 A-to-I Human chr22 + 21691423 21691423 21691423 CAGGAGGAGGCCAGGCGCGGTGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCCGAGGCAGGC CAGGAGGAGGCCAGGCGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGC A G PPIL2 Ensembl:ENSG00000100023 Protein coding intron GSE100210 HepG2 cell line chr22:21691422..21691423 29129909 RNA-Seq:(High) rs1022432665 Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 4 prostate RMVar_hsa_circ_267588,RMVar_hsa_circ_340989 52955 RMVar_ID_52955 Human_SNP_ID_844250185 A-to-I Human chr22 + 17066029 17066029 17066029 TAAAAAATTATTGGATGTGGTGGTGCATGCCTATAGTCCCAGCTACTTGGGAGGCTGAGGCAGGA TAAAAAATTATTGGATGTGGTGGTGCATGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGA A G - - Other Unknown GSE100210 HepG2 cell line chr22:17066028..17066029 29129909 RNA-Seq:(High) rs1159352127 Functional Loss SNV ICGC 33..33 33 LICA 1 - 52956 RMVar_ID_52956 Human_SNP_ID_844257446 A-to-I Human chr22 - 40846118 40846118 40846118 CAGCCTGACTAACATGGAGAAACCCCATCTCTACTAAAAATACAAAATTAGCCAGGTGTGGTGAC CAGCCTGACTAACATGGAGAAACCCCATCTCTGCTAAAAATACAAAATTAGCCAGGTGTGGTGAC T C ST13 Ensembl:ENSG00000100380 Protein coding intron GSE38233 cultured B-cells chr22:40846117..40846118 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 3 breast RMVar_hsa_circ_59280,RMVar_hsa_circ_354126,RMVar_hsa_circ_378365,RMVar_hsa_circ_214510,RMVar_hsa_circ_306891,RMVar_hsa_circ_288392,RMVar_hsa_circ_214511,RMVar_hsa_circ_327098,RMVar_hsa_circ_359540,RMVar_hsa_circ_214512 52957 RMVar_ID_52957 Human_SNP_ID_844261909 A-to-I Human chr22 - 41064276 41064276 41064276 ACCCCAATGCAGACCAGCCGCCACAGCAGGGCATTGCCTTCGAACAGACGCCGTGGGTCCTTCTG ACCCCAATGCAGACCAGCCGCCACAGCAGGGCGTTGCCTTCGAACAGACGCCGTGGGTCCTTCTG T C L13705-009,L13304-001 RNACentral:URS00001E2917,RNACentral:URS000044B5AA misc_RNA,scRNA intron,intron GSE100210 HepG2 cell line chr22:41064275..41064276 29129909 RNA-Seq:(High) rs879050166 Functional Loss SNV ICGC 33..33 33 BRCA 1 - 52958 RMVar_ID_52958 Human_SNP_ID_844269841 A-to-I Human chr22 + 49925522 49925522 49925522 CTACGTCTGTGTGTGTCCTGACGGCTTCGAAGAAACGGAAGATGCCTGTGTGCCGCCGGCAGAGG CTACGTCTGTGTGTGTCCTGACGGCTTCGAAGGAACGGAAGATGCCTGTGTGCCGCCGGCAGAGG A G CRELD2 Ensembl:ENSG00000184164 Protein coding CDS GSE100210 HepG2 cell line chr22:49925521..49925522 29129909 RNA-Seq:(High) rs11545763 Functional Loss SNV ICGC,COSMIC 33..33 33 stomach adenocarcinoma,LUSC,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 9 stomach,haematopoietic and lymphoid tissue Human_RBP_ID_583196,Human_RBP_ID_3962511,Human_RBP_ID_17660671,Human_RBP_ID_22454777,Human_RBP_ID_23954033,Human_RBP_ID_26346152 Human_Splice_Rec_2178193,Human_Splice_Rec_2178211,Human_Splice_Rec_2178243,Human_Splice_Rec_2178259,Human_Splice_Rec_2178291 Clinvar_Rec_38 GWAS_ID_227,GWAS_ID_228,GWAS_ID_229,GWAS_ID_230,GWAS_ID_231,GWAS_ID_232,GWAS_ID_233,GWAS_ID_234,GWAS_ID_235,GWAS_ID_236,GWAS_ID_237,GWAS_ID_238,GWAS_ID_239,GWAS_ID_240,GWAS_ID_241,GWAS_ID_242,GWAS_ID_243,GWAS_ID_244,GWAS_ID_245,GWAS_ID_246,GWAS_ID_247,GWAS_ID_248,GWAS_ID_249,GWAS_ID_250,GWAS_ID_251,GWAS_ID_252,GWAS_ID_253,GWAS_ID_254,GWAS_ID_255,GWAS_ID_256,GWAS_ID_257,GWAS_ID_258,GWAS_ID_259,GWAS_ID_260 52959 RMVar_ID_52959 Human_SNP_ID_844282846 A-to-I Human chr22 + 39031023 39031023 39031023 CCCTGTCTCTACTAAAACTACAAAAATTAGCCAGGCGTAGGAGTGCGCGACTGTAATCCTAGCTA CCCTGTCTCTACTAAAACTACAAAAATTAGCCCGGCGTAGGAGTGCGCGACTGTAATCCTAGCTA A C APOBEC3D,AL022318.4 Ensembl:ENSG00000243811,Ensembl:ENSG00000284554 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells chr22:39031022..39031023 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 52960 RMVar_ID_52960 Human_SNP_ID_844284058 A-to-I Human chr22 - 46713724 46713724 46713724 TGCTCCTGGGTGGAAGCCTCCAGTCTCTCTGCATACTGTTTTCACATTGATTCATGTTGGTCGCA TGCTCCTGGGTGGAAGCCTCCAGTCTCTCTGCGTACTGTTTTCACATTGATTCATGTTGGTCGCA T C CERK Ensembl:ENSG00000100422 Protein coding intron GSE38233 cultured B-cells chr22:46713723..46713724 24183664 RNA-Seq:(High) rs13054785 Functional Loss SNV ICGC 33..33 33 ESCA 1 - GWAS_ID_223,GWAS_ID_224,GWAS_ID_225,GWAS_ID_226 RMVar_hsa_circ_18547,RMVar_hsa_circ_268955,RMVar_hsa_circ_25482,RMVar_hsa_circ_330381,RMVar_hsa_circ_719,RMVar_hsa_circ_127219,RMVar_hsa_circ_334074,RMVar_hsa_circ_344224,RMVar_hsa_circ_215144,RMVar_hsa_circ_215145 52961 RMVar_ID_52961 Human_SNP_ID_844293682 A-to-I Human chr22 - 38695650 38695650 38695650 TTCAGTCCAGCAGTTTGAGACCAGCCCGTGCAACATAGTGAGACCCTATCTCTACAAAAAATTTA TTCAGTCCAGCAGTTTGAGACCAGCCCGTGCAGCATAGTGAGACCCTATCTCTACAAAAAATTTA T C JOSD1 Ensembl:ENSG00000100221 Protein coding intron GSE100210 HepG2 cell line chr22:38695649..38695650 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 52962 RMVar_ID_52962 Human_SNP_ID_844307190 A-to-I Human chr22 + 37866574 37866574 37866574 TTGGGAAGCCAAGGCGGGTGGATCACGAGGTCAGGAGTTCGAGACCAGCCTGACCAACATGGTGA TTGGGAAGCCAAGGCGGGTGGATCACGAGGTCCGGAGTTCGAGACCAGCCTGACCAACATGGTGA A C EIF3L Ensembl:ENSG00000100129 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr22:37866573..37866574 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 9 ovary 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_214237,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_214238 52963 RMVar_ID_52963 Human_SNP_ID_844321864 A-to-I Human chr22 + 37660325 37660325 37660325 GCCTCCATCCTGCCTCTGGGAATTGGTGTTTCAGCCCTCACAAGTAGGGACAGTCCTCGCAGGCT GCCTCCATCCTGCCTCTGGGAATTGGTGTTTCGGCCCTCACAAGTAGGGACAGTCCTCGCAGGCT A G Z83844.3,PDXP Ensembl:ENSG00000285304,Ensembl:ENSG00000241360 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells chr22:37660324..37660325 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_22725456 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 52964 RMVar_ID_52964 Human_SNP_ID_844329076 A-to-I Human chr22 - 23643335 23643335 23643335 GGCTGGGCATGGTGGCTCACGCCTGTAATTCCAGGACTTTGGGAGGCCCAGGTGGGCAGATCACT GGCTGGGCATGGTGGCTCACGCCTGTAATTCCTGGACTTTGGGAGGCCCAGGTGGGCAGATCACT T A GUSBP11 Ensembl:ENSG00000228315 lincRNA intron GSE100210 HepG2 cell line chr22:23643334..23643335 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_22725423 52965 RMVar_ID_52965 Human_SNP_ID_844332539 A-to-I Human chr22 - 31740531 31740529 31740531 CATATCAAAACTTTGTCTCCACCAAAAAAAAAAATTAGCCAGGTGTGGCCTGGCACAGTGACTCA CATATCAAAACTTTGTCTCCACCAAAAAAAAA__TTAGCCAGGTGTGGCCTGGCACAGTGACTCA ATT A PRR14L Ensembl:ENSG00000183530 Protein coding intron GSE47997 K562 cells&HepG2 cells chr22:31740530..31740531 23474544 RNA-Seq:(High) - Functional Loss DEL ICGC 33..34 33 COCA 1 - Human_RBP_ID_14462158 52966 RMVar_ID_52966 Human_SNP_ID_844332667 A-to-I Human chr22 - 19427112 19427112 19427112 GCCCACTCATGGAGAATTATCTAGCCCCAAATATCAATAGTGCTAAGGGTGAGAAACCCCGCTCT GCCCACTCATGGAGAATTATCTAGCCCCAAATGTCAATAGTGCTAAGGGTGAGAAACCCCGCTCT T C HIRA,C22orf39 Ensembl:ENSG00000100084,Ensembl:ENSG00000242259 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line chr22:19427111..19427112 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_2712375 RMVar_hsa_circ_212937,RMVar_hsa_circ_115706 52967 RMVar_ID_52967 Human_SNP_ID_844348329 A-to-I Human chr22 - 35930750 35930750 35930750 TCTTGGCTTACTGCAACCTCCGCCTCCTGGGTACAAGTGATTCTTGTGCCTCATCCTCCCCTGTA TCTTGGCTTACTGCAACCTCCGCCTCCTGGGTGCAAGTGATTCTTGTGCCTCATCCTCCCCTGTA T C RBFOX2 Ensembl:ENSG00000100320 Protein coding intron GSE107867 ASD brains,frontal_cortex chr22:35930749..35930750 30559470 RNA-Seq:(High) rs1325905800 Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 3 prostate RMVar_hsa_circ_337746 52968 RMVar_ID_52968 Human_SNP_ID_844349668 A-to-I Human chr22 + 29230813 29230813 29230813 GTCTCTACAAATAATTTTTTTTTAAATTTGCCATGTGTGGTGGTGCATCCCTGTGGTCCCAGCTA GTCTCTACAAATAATTTTTTTTTAAATTTGCCGTGTGTGGTGGTGCATCCCTGTGGTCCCAGCTA A G EMID1 Ensembl:ENSG00000186998 Protein coding intron GSE38233 cultured B-cells chr22:29230812..29230813 24183664 RNA-Seq:(High) rs3765296 Functional Loss SNV ICGC 33..33 33 ESCA 1 - 52969 RMVar_ID_52969 Human_SNP_ID_844354034 A-to-I Human chr22 + 35301071 35301066 35301071 CCGTCTCTACAAAAAAAAAAAAAAAAAAAAATACAGAAATTAGCCGGGCGTGGTGGTGCGTGCCT CCGTCTCTACAAAAAAAAAAAAAAAAAA_____CAGAAATTAGCCGGGCGTGGTGGTGCGTGCCT AAAATA A TOM1 Ensembl:ENSG00000100284 Protein coding intron GSE100210 HepG2 cell line chr22:35301070..35301071 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 29..33 33 LMS 1 - 52970 RMVar_ID_52970 Human_SNP_ID_844361518 A-to-I Human chr22 + 41211473 41211473 41211473 AGTGATCCCCCACCTCAGCCTCCCAAAGTGCTAGGATTACAGGCATGAGCCACCGCACCCAGCCC AGTGATCCCCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCACCCAGCCC A G L3MBTL2 Ensembl:ENSG00000100395 Protein coding intron GSE100210 HepG2 cell line chr22:41211472..41211473 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_72377,RMVar_hsa_circ_107484,RMVar_hsa_circ_214598,RMVar_hsa_circ_56689 52971 RMVar_ID_52971 Human_SNP_ID_844362652 A-to-I Human chr22 + 37868253 37868253 37868253 TTTCCTGCCTCAGCTTCCCAAGTATCTGGATTACAGGTGTGCACCACCACGCCCTGCTAATTTTT TTTCCTGCCTCAGCTTCCCAAGTATCTGGATTTCAGGTGTGCACCACCACGCCCTGCTAATTTTT A T EIF3L Ensembl:ENSG00000100129 Protein coding intron GSE100210 HepG2 cell line chr22:37868252..37868253 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 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_214237,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_214238 52972 RMVar_ID_52972 Human_SNP_ID_844372719 A-to-I Human chr22 - 42828853 42828853 42828853 TTGCAGGACCCTATCTCTACTAAAAATACAAAAATTAGCCAGGCATGGTGGTGCATGCCTGTAAT TTGCAGGACCCTATCTCTACTAAAAATACAAACATTAGCCAGGCATGGTGGTGCATGCCTGTAAT T G ARFGAP3 Ensembl:ENSG00000242247 Protein coding intron GSE100210 HepG2 cell line chr22:42828852..42828853 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_214819,RMVar_hsa_circ_22634,RMVar_hsa_circ_15451,RMVar_hsa_circ_287958,RMVar_hsa_circ_214812,RMVar_hsa_circ_346051,RMVar_hsa_circ_69170,RMVar_hsa_circ_214815,RMVar_hsa_circ_87698,RMVar_hsa_circ_327237,RMVar_hsa_circ_100099,RMVar_hsa_circ_28705,RMVar_hsa_circ_68745,RMVar_hsa_circ_60259,RMVar_hsa_circ_214818,RMVar_hsa_circ_317501,RMVar_hsa_circ_318145,RMVar_hsa_circ_214823,RMVar_hsa_circ_329883,RMVar_hsa_circ_274758,RMVar_hsa_circ_214824,RMVar_hsa_circ_214825 52973 RMVar_ID_52973 Human_SNP_ID_844381697 A-to-I Human chr22 - 49813199 49813199 49813199 AAAAATAGAGATGGCGTCTCACTGTGTTGCCTAGGTTGGTCTTGAACTCCTGAGCTCAAATGATC AAAAATAGAGATGGCGTCTCACTGTGTTGCCTGGGTTGGTCTTGAACTCCTGAGCTCAAATGATC T C BRD1 Ensembl:ENSG00000100425 Protein coding intron GSE100210 HepG2 cell line chr22:49813198..49813199 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 RECA 1 - Human_RBP_ID_14527631 RMVar_hsa_circ_265202,RMVar_hsa_circ_360593,RMVar_hsa_circ_75323,RMVar_hsa_circ_28290,RMVar_hsa_circ_343990 52974 RMVar_ID_52974 Human_SNP_ID_844386370 A-to-I Human chr22 + 41142713 41142713 41142713 GGAGACCATCCTGGCTAACACGGTGAAACCCCATCTCTACTAAAAATACAAAACAATTAGCCGGG GGAGACCATCCTGGCTAACACGGTGAAACCCCGTCTCTACTAAAAATACAAAACAATTAGCCGGG A G EP300 Ensembl:ENSG00000100393 Protein coding intron GSE38233 cultured B-cells chr22:41142712..41142713 24183664 RNA-Seq:(High) rs1172933253 Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_214543,RMVar_hsa_circ_61612,RMVar_hsa_circ_96967,RMVar_hsa_circ_214537,RMVar_hsa_circ_360687,RMVar_hsa_circ_357085,RMVar_hsa_circ_357569,RMVar_hsa_circ_289966,RMVar_hsa_circ_125932,RMVar_hsa_circ_120724,RMVar_hsa_circ_80226,RMVar_hsa_circ_89813,RMVar_hsa_circ_214547,RMVar_hsa_circ_214548,RMVar_hsa_circ_214545,RMVar_hsa_circ_214546,RMVar_hsa_circ_214544,RMVar_hsa_circ_100237,RMVar_hsa_circ_214557,RMVar_hsa_circ_102183,RMVar_hsa_circ_101874,RMVar_hsa_circ_214558,RMVar_hsa_circ_74330,RMVar_hsa_circ_214559,RMVar_hsa_circ_122834,RMVar_hsa_circ_267084,RMVar_hsa_circ_114332,RMVar_hsa_circ_67686,RMVar_hsa_circ_281247,RMVar_hsa_circ_214565,RMVar_hsa_circ_214566,RMVar_hsa_circ_265093,RMVar_hsa_circ_214569,RMVar_hsa_circ_320234,RMVar_hsa_circ_214573,RMVar_hsa_circ_214574,RMVar_hsa_circ_357329,RMVar_hsa_circ_365393,RMVar_hsa_circ_360639,RMVar_hsa_circ_124497 52975 RMVar_ID_52975 Human_SNP_ID_844397059 A-to-I Human chr22 - 41599288 41599288 41599288 TTAGTTAGATTTTGGGAAAGTGAGCATGAAGAAGGGACTCAGAGCTGCCAGGTACCCGAGTCTCA TTAGTTAGATTTTGGGAAAGTGAGCATGAAGATGGGACTCAGAGCTGCCAGGTACCCGAGTCTCA T A DESI1 Ensembl:ENSG00000100418 Protein coding 3'UTR GSE100210 HepG2 cell line chr22:41599287..41599288 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_581617,Human_RBP_ID_1943765,Human_RBP_ID_7087240,Human_RBP_ID_14507703 Human_miRNA_ID_544884,Human_miRNA_ID_580119,Human_miRNA_ID_583088,Human_miRNA_ID_2211001 RMVar_hsa_circ_100552,RMVar_hsa_circ_108119,RMVar_hsa_circ_110812,RMVar_hsa_circ_214696,RMVar_hsa_circ_214697,RMVar_hsa_circ_214698 52976 RMVar_ID_52976 Human_SNP_ID_844453702 A-to-I Human chr22 - 41938341 41938341 41938341 AAAAAAAAAAGCGAGACCAGCCTGGCCAACATAGTGAAACCCTGTCTCTACTAAAAATACAAAAA AAAAAAAAAAGCGAGACCAGCCTGGCCAACATGGTGAAACCCTGTCTCTACTAAAAATACAAAAA T C - - Other Unknown GSE100210 HepG2 cell line chr22:41938340..41938341 29129909 RNA-Seq:(High) rs1400167351 Functional Loss SNV ICGC 33..33 33 PAAD 1 - 52977 RMVar_ID_52977 Human_SNP_ID_844460676 A-to-I Human chr22 - 49806075 49806075 49806075 CGAGACCAGCCTGGCCAACATAGCAAAACCCCATCTTCACTGAAAACATAAAAATTAGCTGGGTG CGAGACCAGCCTGGCCAACATAGCAAAACCCCGTCTTCACTGAAAACATAAAAATTAGCTGGGTG T C BRD1 Ensembl:ENSG00000100425 Protein coding intron GSE38233 cultured B-cells chr22:49806074..49806075 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 5 breast RMVar_hsa_circ_265202,RMVar_hsa_circ_360593,RMVar_hsa_circ_75323,RMVar_hsa_circ_28290,RMVar_hsa_circ_343990 52978 RMVar_ID_52978 Human_SNP_ID_844496374 A-to-I Human chr22 + 24576267 24576267 24576267 TGTCTGTGGTTTTTCTTTTTCTTTTTTTTTTTAAAGACTGAGTTTCACGCTTGTTGCCCAGGCTG TGTCTGTGGTTTTTCTTTTTCTTTTTTTTTTTTAAGACTGAGTTTCACGCTTGTTGCCCAGGCTG A T SNRPD3,GGT1 Ensembl:ENSG00000100028,Ensembl:ENSG00000286070 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line chr22:24576266..24576267;chr22:24576267..24576268 29129909 RNA-Seq:(High) rs1158646814 Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_576841,Human_RBP_ID_2713683,Human_RBP_ID_7067069,Human_RBP_ID_14420487 52979 RMVar_ID_52979 Human_SNP_ID_844582520 A-to-I Human chr22 - 32039647 32039647 32039647 CCTCTCTGAATCCATTTCATCAGATGCGTGACATAGCCTGCTATCTTGTTGCGGAGCTTCTTGCT CCTCTCTGAATCCATTTCATCAGATGCGTGACGTAGCCTGCTATCTTGTTGCGGAGCTTCTTGCT T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank;ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr22:32039646..32039647 30559470 RNA-Seq:(High) rs539008116 Functional Loss SNV ICGC 33..33 33 STAD 1 - 52980 RMVar_ID_52980 Human_SNP_ID_844604974 A-to-I Human chr22 - 24648742 24648742 24648742 AGGGTGATGCAGAGGCCACAGGTGCTGCACGCACCAGCACCCGCTCTAGACATCAGCCTCCAGGT AGGGTGATGCAGAGGCCACAGGTGCTGCACGCGCCAGCACCCGCTCTAGACATCAGCCTCCAGGT T C AP000356.2 Ensembl:ENSG00000284070 lincRNA exon GSE47997 K562 cells&HepG2 cells chr22:24648741..24648742 23474544 RNA-Seq:(High) rs879126994 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 52981 RMVar_ID_52981 Human_SNP_ID_844626391 A-to-I Human chr22 + 37869331 37869331 37869331 GTTTGTGTTTTTTATAGCGATAGGGTTTTGCCATGTTTCCCAGGCTGGTCTTGAGCTCCTGGACC GTTTGTGTTTTTTATAGCGATAGGGTTTTGCCGTGTTTCCCAGGCTGGTCTTGAGCTCCTGGACC A G EIF3L Ensembl:ENSG00000100129 Protein coding intron GSE100210 HepG2 cell line chr22:37869330..37869331 29129909 RNA-Seq:(High) rs188722004 Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 5 oesophagus Human_RBP_ID_14479053 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_214237,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_214238 52982 RMVar_ID_52982 Human_SNP_ID_844633609 A-to-I Human chr22 + 29293730 29293730 29293730 AGGATTACAGGTGCCCGCCACCACACCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTGG AGGATTACAGGTGCCCGCCACCACACCCAGCTGATTTTTGTATTTTTAGTAGAGATGGGGTTTGG A G EWSR1 Ensembl:ENSG00000182944 Protein coding intron GSE38233 cultured B-cells chr22:29293729..29293730 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_38608 52983 RMVar_ID_52983 Human_SNP_ID_844659025 A-to-I Human chr22 + 31236454 31236453 31236454 AACAGAGCAAGACCTCATCCCCACAAAAAATCAAAAATTTAGCCAGGCATGGTGGCTCATGCCTG AACAGAGCAAGACCTCATCCCCACAAAAAATC_AAAATTTAGCCAGGCATGGTGGCTCATGCCTG CA C LIMK2 Ensembl:ENSG00000182541 Protein coding intron GSE100210 HepG2 cell line chr22:31236453..31236454 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_50381,RMVar_hsa_circ_213789,RMVar_hsa_circ_94950,RMVar_hsa_circ_350119 52984 RMVar_ID_52984 Human_SNP_ID_844670700 A-to-I Human chr22 - 50277979 50277979 50277979 CACACTGCAGCAGTTTGTGGACAACTTCTTCCAGAGCGTGCTGGCGCCTGGGCACGCGGTGCCAC CACACTGCAGCAGTTTGTGGACAACTTCTTCCTGAGCGTGCTGGCGCCTGGGCACGCGGTGCCAC T A PLXNB2 Ensembl:ENSG00000196576 Protein coding exon GSE100210 HepG2 cell line chr22:50277978..50277979 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 5 lung Human_RBP_ID_18194225,Human_RBP_ID_22455086 Human_Splice_Rec_2179774,Human_Splice_Rec_2179810,Human_Splice_Rec_2179850,Human_Splice_Rec_2179922,Human_Splice_Rec_2179994,Human_Splice_Rec_2180026,Human_Splice_Rec_2180052,Human_Splice_Rec_2180062 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_93675,RMVar_hsa_circ_110360,RMVar_hsa_circ_86027,RMVar_hsa_circ_117818,RMVar_hsa_circ_215252,RMVar_hsa_circ_215256,RMVar_hsa_circ_215258,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 52985 RMVar_ID_52985 Human_SNP_ID_844681586 A-to-I Human chr22 + 45332923 45332923 45332923 GCGCCACCATGCCTGGCTAATTTTGTATTTTTAGTAGAGATAGGGTTTCACCATGTTGGTCAGGC GCGCCACCATGCCTGGCTAATTTTGTATTTTTGGTAGAGATAGGGTTTCACCATGTTGGTCAGGC A G FAM118A Ensembl:ENSG00000100376 Protein coding intron GSE38233 cultured B-cells chr22:45332922..45332923 24183664 RNA-Seq:(High) rs910575512 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 3 liver RMVar_hsa_circ_56853,RMVar_hsa_circ_68942,RMVar_hsa_circ_214978,RMVar_hsa_circ_93063,RMVar_hsa_circ_214979,RMVar_hsa_circ_347303 52986 RMVar_ID_52986 Human_SNP_ID_844696390 A-to-I Human chr22 + 50207392 50207392 50207392 GTGATTCACCCATCTTGGCCTCCTAAAGTGCTAGAATTATAGGCCTGAGCCACCGCGCCCGGCCC GTGATTCACCCATCTTGGCCTCCTAAAGTGCTGGAATTATAGGCCTGAGCCACCGCGCCCGGCCC A G SELENOO Ensembl:ENSG00000073169 Protein coding intron GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;Bronchiolar epithelium,BEP2D cell line chr22:50207391..50207392 29129909,30559470,31158229 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_18792139 RMVar_hsa_circ_332091,RMVar_hsa_circ_215217 52987 RMVar_ID_52987 Human_SNP_ID_844745957 A-to-I Human chr22 - 42890618 42890618 42890618 CTGTGCCTCCTGGGTTCAAGCAATTCTGCCTCAGCCCTCCGAGTAGCTGGGACTACCGGCACATG CTGTGCCTCCTGGGTTCAAGCAATTCTGCCTCGGCCCTCCGAGTAGCTGGGACTACCGGCACATG T C PACSIN2 Ensembl:ENSG00000100266 Protein coding intron GSE38233 cultured B-cells chr22:42890617..42890618 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_366692,RMVar_hsa_circ_81967,RMVar_hsa_circ_85728,RMVar_hsa_circ_214835,RMVar_hsa_circ_214836,RMVar_hsa_circ_214834,RMVar_hsa_circ_214840,RMVar_hsa_circ_47789,RMVar_hsa_circ_60137,RMVar_hsa_circ_122735,RMVar_hsa_circ_340192,RMVar_hsa_circ_214839,RMVar_hsa_circ_126629,RMVar_hsa_circ_264836 52988 RMVar_ID_52988 Human_SNP_ID_844789124 A-to-I Human chr22 + 39033060 39033060 39033060 CACGACAAAGCCCCATTTCTACAAAAAAAAATACCAAAAAAAAGCCAGATGTGGTGGCATGCACC CACGACAAAGCCCCATTTCTACAAAAAAAAATTCCAAAAAAAAGCCAGATGTGGTGGCATGCACC A T APOBEC3D,AL022318.4 Ensembl:ENSG00000243811,Ensembl:ENSG00000284554 Protein coding,Protein coding 3'UTR,3'UTR GSE47997 K562 cells&HepG2 cells chr22:39033059..39033060 23474544 RNA-Seq:(High) rs1031010211 Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 4 pancreas 52989 RMVar_ID_52989 Human_SNP_ID_844793045 A-to-I Human chr22 + 47174625 47174625 47174625 TGTGACTGGTTCCATCATGGACCGGTTCCTCCATGGACCGGTTCCTCCGTGGACCGGTTCCGCCA TGTGACTGGTTCCATCATGGACCGGTTCCTCCGTGGACCGGTTCCTCCGTGGACCGGTTCCGCCA A G TBC1D22A Ensembl:ENSG00000054611 Protein coding 3'UTR GSE38233 cultured B-cells chr22:47174624..47174625 24183664 RNA-Seq:(High) rs56869004 Functional Loss SNV ICGC,COSMIC 33..33 33 SKCA,haematopoietic_and_lymphoid_tissue mycosis_fungoides-Sezary_syndrome,skin mycosis_fungoides-Sezary_syndrome,liver hepatocellular_carcinoma 8 liver,skin,haematopoietic and lymphoid tissue 52990 RMVar_ID_52990 Human_SNP_ID_844795639 A-to-I Human chr22 - 42108411 42108411 42108411 CTGTGAGAGGAGGAGATAAAAAACTAAAACCCAAATATGATATAATGTGCAAAGTAAAATCCTGG CTGTGAGAGGAGGAGATAAAAAACTAAAACCCGAATATGATATAATGTGCAAAGTAAAATCCTGG T C OLA1P1 Ensembl:ENSG00000213790 Pseudogene exon GSE107867 ASD brains,frontal_cortex chr22:42108410..42108411 30559470 RNA-Seq:(High) rs878925875 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_17583817,Human_RBP_ID_26499204 52991 RMVar_ID_52991 Human_SNP_ID_844803908 A-to-I Human chr22 - 46685158 46685154 46685158 GCTGAGGCAGGAGAATCGCTTGAACCCAAGAAAGAGGTGGAGGTTGCGGTGAGCCAAGATTGCGC GCTGAGGCAGGAGAATCGCTTGAACCCAAGAA____GTGGAGGTTGCGGTGAGCCAAGATTGCGC CCTCT C CERK Ensembl:ENSG00000100422 Protein coding 3'UTR GSE100210 HepG2 cell line chr22:46685157..46685158 29129909 RNA-Seq:(High) rs1463365962 Functional Loss DEL ICGC 33..36 33 LMS 1 - RMVar_hsa_circ_268955 52992 RMVar_ID_52992 Human_SNP_ID_844807064 A-to-I Human chr22 + 38004474 38004474 38004474 CGCTCACTGTGGGCCAGGTGCTTTCTACCTATAAGACATGCATATCTACTCGCTGAGTTCTCATG CGCTCACTGTGGGCCAGGTGCTTTCTACCTATTAGACATGCATATCTACTCGCTGAGTTCTCATG A T POLR2F Ensembl:ENSG00000100142 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,frontal_cortex chr22:38004474..38004475 29129909,30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 52993 RMVar_ID_52993 Human_SNP_ID_827875061 A-to-I Human chr17 + 5426740 5426738 5426740 TAGGCTCACTGCAACCTCTGCCTTGCGGGTTCAAGTCATTCTCCTGCCTCAGCCTCCCAAGTAGC TAGGCTCACTGCAACCTCTGCCTTGCGGGTT__AGTCATTCTCCTGCCTCAGCCTCCCAAGTAGC TCA T RPAIN Ensembl:ENSG00000129197 Protein coding intron GSE100210 HepG2 cell line chr17:5426740..5426741 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 32..33 33 LMS 1 - Human_RBP_ID_8457345,Human_RBP_ID_13080701 RMVar_hsa_circ_6190 52994 RMVar_ID_52994 Human_SNP_ID_827875651 A-to-I Human chr17 - 15503157 15503157 15503157 GCTCAAGAGATCCTCCCGCTTCCGCCTTCCAAAGCGCTGGGATAACAGGCGTGAGCCGCTGCCCG GCTCAAGAGATCCTCCCGCTTCCGCCTTCCAAGGCGCTGGGATAACAGGCGTGAGCCGCTGCCCG T C TVP23C-CDRT4,CDRT4,TVP23C Ensembl:ENSG00000259024,Ensembl:ENSG00000239704,Ensembl:ENSG00000175106 Protein coding,Protein coding,Protein coding intron,5'UTR,CDS GSE100210;GSE107867;GSE107867 HepG2 cell line;ASD brains,cerebellum;ASD brains,frontal_cortex chr17:15503156..15503157 29129909,30559470,30559470 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 2 lung Human_RBP_ID_5088285,Human_RBP_ID_25336045 Human_Splice_Rec_1782007,Human_Splice_Rec_1782032,Human_Splice_Rec_1782033,Human_Splice_Rec_1782066 52995 RMVar_ID_52995 Human_SNP_ID_827966198 A-to-I Human chr17 - 32228073 32228073 32228073 ATCGAGGTTGTTTGCAACGACCGTCTGGGGAAAAAGGTCCACGTTAAATGCAACACGGATGATAC ATCGAGGTTGTTTGCAACGACCGTCTGGGGAAGAAGGTCCACGTTAAATGCAACACGGATGATAC T C UBL5P2 Ensembl:ENSG00000266282 Pseudogene exon GSE100210 HepG2 cell line chr17:32228072..32228073 29129909 RNA-Seq:(High) rs879037419 Functional Loss SNV ICGC 33..33 33 LAML 2 - 52996 RMVar_ID_52996 Human_SNP_ID_827996741 A-to-I Human chr17 - 46147417 46147417 46147417 GGCGCATGCTACCACATCTGGCTAATTTTTGTATTTTTTGTAGAGACAGGATCTTGCCACCTTGC GGCGCATGCTACCACATCTGGCTAATTTTTGTGTTTTTTGTAGAGACAGGATCTTGCCACCTTGC T C KANSL1 Ensembl:ENSG00000120071 Protein coding intron GSE100210 HepG2 cell line chr17:46147416..46147417 29129909 RNA-Seq:(High) rs1400265584 Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 6 prostate Human_RBP_ID_2509358,Human_RBP_ID_13037822 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 52997 RMVar_ID_52997 Human_SNP_ID_827999828 A-to-I Human chr17 + 59201699 59201699 59201699 ACAAATACAGATAAAAACACCCAGCTGGGTGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGG ACAAATACAGATAAAAACACCCAGCTGGGTGCCGTGGCTCACACCTGTAATCCCAGCACTTTGGG A C AC099850.3,PRR11 Ensembl:ENSG00000265303,Ensembl:ENSG00000068489 Protein coding,Protein coding intron,3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr17:59201698..59201699 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 5 lung Human_Splice_Rec_1847035,Human_Splice_Rec_1847077,Human_Splice_Rec_1847097 Human_miRNA_ID_619845,Human_miRNA_ID_1472912,Human_miRNA_ID_2891094 RMVar_hsa_circ_97892,RMVar_hsa_circ_185763 52998 RMVar_ID_52998 Human_SNP_ID_827999831 A-to-I Human chr17 + 59201699 59201699 59201699 ACAAATACAGATAAAAACACCCAGCTGGGTGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGG ACAAATACAGATAAAAACACCCAGCTGGGTGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGG A G AC099850.3,PRR11 Ensembl:ENSG00000265303,Ensembl:ENSG00000068489 Protein coding,Protein coding intron,3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr17:59201698..59201699 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_Splice_Rec_1847035,Human_Splice_Rec_1847077,Human_Splice_Rec_1847097 Human_miRNA_ID_619845,Human_miRNA_ID_1472912,Human_miRNA_ID_2891094 RMVar_hsa_circ_97892,RMVar_hsa_circ_185763 52999 RMVar_ID_52999 Human_SNP_ID_828039956 A-to-I Human chr17 + 1776511 1776511 1776511 CCCCGGCTTTTGGGCTCTGAAGGACTAACCACATGCTTTCTCACTTGTCTCAGATTGCCCAGCTG CCCCGGCTTTTGGGCTCTGAAGGACTAACCACGTGCTTTCTCACTTGTCTCAGATTGCCCAGCTG A G SERPINF1 Ensembl:ENSG00000132386 Protein coding intron GSE38233 cultured B-cells chr17:1776510..1776511 24183664 RNA-Seq:(High) rs2071022 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma,liver hepatocellular_carcinoma 8 liver,large intestine Human_RBP_ID_22657237 Clinvar_Rec_128 GWAS_ID_5485,GWAS_ID_5486,GWAS_ID_5487,GWAS_ID_5488,GWAS_ID_5489,GWAS_ID_5490,GWAS_ID_5491,GWAS_ID_5492,GWAS_ID_5493,GWAS_ID_5494,GWAS_ID_5495,GWAS_ID_5496,GWAS_ID_5497,GWAS_ID_5498,GWAS_ID_5499,GWAS_ID_5500,GWAS_ID_5501,GWAS_ID_5502,GWAS_ID_5503,GWAS_ID_5504,GWAS_ID_5505,GWAS_ID_5506,GWAS_ID_5507 RMVar_hsa_circ_98676,RMVar_hsa_circ_181146 53000 RMVar_ID_53000 Human_SNP_ID_828052020 A-to-I Human chr17 - 1781216 1781216 1781216 ATGGAACACAAGTTAAAGAGGTTTTGCTGGCCAGGTATGGTGGCTCACGCCTGTAATCCCAGCAC ATGGAACACAAGTTAAAGAGGTTTTGCTGGCCGGGTATGGTGGCTCACGCCTGTAATCCCAGCAC T C SMYD4 Ensembl:ENSG00000186532 Protein coding 3'UTR GSE38233 cultured B-cells chr17:1781215..1781216 24183664 RNA-Seq:(High) rs958807063 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 2 liver Human_miRNA_ID_1810220 RMVar_hsa_circ_96490,RMVar_hsa_circ_98361,RMVar_hsa_circ_181148,RMVar_hsa_circ_80652,RMVar_hsa_circ_181149,RMVar_hsa_circ_181147 53001 RMVar_ID_53001 Human_SNP_ID_828054619 A-to-I Human chr17 - 1349108 1349108 1349108 TCAATCTCCTAACCTCGTGATCCACCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCCCGAG TCAATCTCCTAACCTCGTGATCCACCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCCCGAG T C YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233 cultured B-cells chr17:1349107..1349108 24183664 RNA-Seq:(High) rs1368322930 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 5 haematopoietic and lymphoid tissue RMVar_hsa_circ_93985,RMVar_hsa_circ_180978 53002 RMVar_ID_53002 Human_SNP_ID_828061372 A-to-I Human chr17 - 38198368 38198368 38198368 AAAAAGTTACTTAGGACTGAGTGCACTGGCTTACGTGTGTAATCCCAGCACTTTGGCAGGCTGAG AAAAAGTTACTTAGGACTGAGTGCACTGGCTTGCGTGTGTAATCCCAGCACTTTGGCAGGCTGAG T C NPEPPSP1 Ensembl:ENSG00000274487 Pseudogene intron GSE100210 HepG2 cell line chr17:38198367..38198368 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_12988549,Human_RBP_ID_17567214 RMVar_hsa_circ_55626,RMVar_hsa_circ_321088,RMVar_hsa_circ_9308 53003 RMVar_ID_53003 Human_SNP_ID_828069170 A-to-I Human chr17 - 49939139 49939139 49939139 TTGGCAGTTTTGGTTAAGGAGACTTTCTTGTCACACTTGGATTTGGGCATTGCACTGAATCCACG TTGGCAGTTTTGGTTAAGGAGACTTTCTTGTCGCACTTGGATTTGGGCATTGCACTGAATCCACG T C - - Other Unknown GSE100210 HepG2 cell line chr17:49939138..49939139 29129909 RNA-Seq:(High) rs1369545107 Functional Loss SNV ICGC 33..33 33 LAML 2 - 53004 RMVar_ID_53004 Human_SNP_ID_828076254 A-to-I Human chr17 - 35511553 35511553 35511553 TATGTGTGTGTGTGTAGAGACGAGGTCTCACCATCTTGCCCAGGCTGGTCTCTAACTCCTGGGCT TATGTGTGTGTGTGTAGAGACGAGGTCTCACCGTCTTGCCCAGGCTGGTCTCTAACTCCTGGGCT T C AC015911.11 Ensembl:ENSG00000286065 lincRNA intron GSE38233 cultured B-cells chr17:35511552..35511553 24183664 RNA-Seq:(High) rs910375770 Functional Loss SNV ICGC 33..33 33 LICA 1 - 53005 RMVar_ID_53005 Human_SNP_ID_828100661 A-to-I Human chr17 - 76486177 76486177 76486177 TGAACCTGGGAAGTGGAGGTTGGCAGTGAGCCAAAATCGCACCACTGCGCTCTAGCCTGGGTGAC TGAACCTGGGAAGTGGAGGTTGGCAGTGAGCCGAAATCGCACCACTGCGCTCTAGCCTGGGTGAC T C RHBDF2 Ensembl:ENSG00000129667 Protein coding intron GSE38233 cultured B-cells chr17:76486176..76486177 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_306022 53006 RMVar_ID_53006 Human_SNP_ID_828115274 A-to-I Human chr17 - 35151325 35151325 35151325 TTAGAATCCCCGCCCCGCGGTGGGGCGCGGGAAATGTGGCGTACGGAAGACCCACTCCCCGGCGC TTAGAATCCCCGCCCCGCGGTGGGGCGCGGGACATGTGGCGTACGGAAGACCCACTCCCCGGCGC T G - - Other Unknown GSE38233 cultured B-cells chr17:35151324..35151325 24183664 RNA-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 53007 RMVar_ID_53007 Human_SNP_ID_828122763 A-to-I Human chr17 + 28722451 28722451 28722451 AGCCTGCCTCAGCCTCCCAAAGTGCTGGGAATACAGCCATGAGCCAGCACACCTGGCCCAGAGAT AGCCTGCCTCAGCCTCCCAAAGTGCTGGGAATGCAGCCATGAGCCAGCACACCTGGCCCAGAGAT A G RPL23A Ensembl:ENSG00000198242 Protein coding intron GSE100210 HepG2 cell line chr17:28722450..28722451 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 oesophagus adenocarcinoma 4 oesophagus Human_RBP_ID_5259960,Human_RBP_ID_6573548,Human_RBP_ID_23167745 RMVar_hsa_circ_75810,RMVar_hsa_circ_81228,RMVar_hsa_circ_183005,RMVar_hsa_circ_124131,RMVar_hsa_circ_183007,RMVar_hsa_circ_92588,RMVar_hsa_circ_183009,RMVar_hsa_circ_183010 53008 RMVar_ID_53008 Human_SNP_ID_828125336 A-to-I Human chr17 - 18271897 18271897 18271897 CACACCCAGCTAATTTGTTTAGTATTTTTAGTAAAGACGGGGTTTCACCATGTTGGCCAGGCTGG CACACCCAGCTAATTTGTTTAGTATTTTTAGTGAAGACGGGGTTTCACCATGTTGGCCAGGCTGG T C TOP3A Ensembl:ENSG00000177302 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr17:18271896..18271897 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 1 - 53009 RMVar_ID_53009 Human_SNP_ID_828128890 A-to-I Human chr17 - 42229731 42229731 42229731 GAGTAGCTGGGACTGCAGGTGCCCGCCACCACACCGAGCTAATTTTTGTATTTTTAATAGAGACG GAGTAGCTGGGACTGCAGGTGCCCGCCACCACGCCGAGCTAATTTTTGTATTTTTAATAGAGACG T C STAT5B Ensembl:ENSG00000173757 Protein coding intron GSE38233 cultured B-cells chr17:42229730..42229731 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 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 53010 RMVar_ID_53010 Human_SNP_ID_828142387 A-to-I Human chr17 + 2604649 2604648 2604649 CCTGGCTAACATGGTGAAGCCCTATCTCTACTAAAAATACACAAATTAGCCGGGCCTGGTGGTGC CCTGGCTAACATGGTGAAGCCCTATCTCTACT_AAAATACACAAATTAGCCGGGCCTGGTGGTGC TA T PAFAH1B1 Ensembl:ENSG00000007168 Protein coding intron GSE38233 cultured B-cells chr17:2604648..2604649 24183664 RNA-Seq:(High) - Functional Loss DEL ICGC 33..33 33 PAAD 1 - RMVar_hsa_circ_181259,RMVar_hsa_circ_81867 53011 RMVar_ID_53011 Human_SNP_ID_828167824 A-to-I Human chr17 - 51190635 51190635 51190635 TCACTGCAGCCTCGACTTCTCGGGTACAAGCAATTCTCCCACCTCAGCCCCTGGAGTAGCTGGGA TCACTGCAGCCTCGACTTCTCGGGTACAAGCAGTTCTCCCACCTCAGCCCCTGGAGTAGCTGGGA T C MBTD1 Ensembl:ENSG00000011258 Protein coding intron GSE38233 cultured B-cells chr17:51190634..51190635 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_22717457 53012 RMVar_ID_53012 Human_SNP_ID_828184411 A-to-I Human chr17 + 62835600 62835598 62835600 CAGCCTGGGAGACAGAATGAGACCCTATCAAGAAAAAAAAAAAAAGAGGAGTGGAGAGAGATCAT CAGCCTGGGAGACAGAATGAGACCCTATCAA__AAAAAAAAAAAAGAGGAGTGGAGAGAGATCAT AGA A MARCHF10-DT Ensembl:ENSG00000265000 lincRNA exon GSE47997 K562 cells&HepG2 cells chr17:62835599..62835600 23474544 RNA-Seq:(High) - Functional Loss DEL ICGC 32..33 33 SKCA 1 - Human_RBP_ID_6659384 53013 RMVar_ID_53013 Human_SNP_ID_828185127 A-to-I Human chr17 + 75788283 75788283 75788283 TTTACTGCAACCTCCACCTCCCGGGTTTAAGCAATTCTCCTGCTTCAGCTTCCTAAGTAGCTGGG TTTACTGCAACCTCCACCTCCCGGGTTTAAGCTATTCTCCTGCTTCAGCTTCCTAAGTAGCTGGG A T UNK Ensembl:ENSG00000132478 Protein coding intron GSE38233 cultured B-cells chr17:75788282..75788283 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_25325048 53014 RMVar_ID_53014 Human_SNP_ID_828185182 A-to-I Human chr17 - 32228065 32228065 32228065 TGTTTGCAACGACCGTCTGGGGAAAAAGGTCCACGTTAAATGCAACACGGATGATACCATCGGGG TGTTTGCAACGACCGTCTGGGGAAAAAGGTCCGCGTTAAATGCAACACGGATGATACCATCGGGG T C UBL5P2 Ensembl:ENSG00000266282 Pseudogene exon GSE100210 HepG2 cell line chr17:32228064..32228065 29129909 RNA-Seq:(High) rs879108495 Functional Loss SNV ICGC 33..33 33 LAML 2 - 53015 RMVar_ID_53015 Human_SNP_ID_828192699 A-to-I Human chr17 - 57046016 57046016 57046016 TCCATAGGGTTTGAGTGCAGGACTCCCCAAGGACCCAGGCTGGGGATGGTGGCGGGCGTGATGAT TCCATAGGGTTTGAGTGCAGGACTCCCCAAGGGCCCAGGCTGGGGATGGTGGCGGGCGTGATGAT T C lnc-COIL-1 RNACentral:URS00008C247A lincRNA intron GSE100210 HepG2 cell line chr17:57046015..57046016 29129909 RNA-Seq:(High) rs1165346473 Functional Loss SNV ICGC 33..33 33 LAML 1 - 53016 RMVar_ID_53016 Human_SNP_ID_828198451 A-to-I Human chr17 + 67973646 67973646 67973646 TCTCCCCTCAGCCTCCCTAGTAGCTGGGATTAAAGGCATGTGCCACCATGCCTGGCTTATTTTTG TCTCCCCTCAGCCTCCCTAGTAGCTGGGATTACAGGCATGTGCCACCATGCCTGGCTTATTTTTG A C BPTF Ensembl:ENSG00000171634 Protein coding intron GSE100210 HepG2 cell line chr17:67973646..67973647 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_48,RMVar_hsa_circ_74181,RMVar_hsa_circ_298433,RMVar_hsa_circ_55441,RMVar_hsa_circ_186705,RMVar_hsa_circ_324311,RMVar_hsa_circ_113175,RMVar_hsa_circ_186723,RMVar_hsa_circ_351769,RMVar_hsa_circ_57588,RMVar_hsa_circ_71713,RMVar_hsa_circ_372814,RMVar_hsa_circ_186744,RMVar_hsa_circ_48311,RMVar_hsa_circ_355915,RMVar_hsa_circ_277900,RMVar_hsa_circ_186757,RMVar_hsa_circ_186759,RMVar_hsa_circ_306916,RMVar_hsa_circ_350921,RMVar_hsa_circ_66730,RMVar_hsa_circ_186760,RMVar_hsa_circ_296250,RMVar_hsa_circ_186762,RMVar_hsa_circ_285319 53017 RMVar_ID_53017 Human_SNP_ID_828214953 A-to-I Human chr17 - 38198173 38198173 38198173 AAATATCCTTTGGCCCAGGCATGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGC AAATATCCTTTGGCCCAGGCATGGTGGCTCACTCCTGTAATCCCAGCACTTTGGGAGGCCGAGGC T A NPEPPSP1 Ensembl:ENSG00000274487 Pseudogene intron GSE100210 HepG2 cell line chr17:38198172..38198173 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_13220612 RMVar_hsa_circ_55626,RMVar_hsa_circ_321088,RMVar_hsa_circ_9308 53018 RMVar_ID_53018 Human_SNP_ID_828239893 A-to-I Human chr17 - 40939701 40939701 40939701 TGTGGTCCCGGCTACTCGGGAGGCTGAGGCAGAAGAATCGCTTGAACCCGGGAGGTGGAGGTTGC TGTGGTCCCGGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCGGGAGGTGGAGGTTGC T C - - Other Unknown GSE100210 HepG2 cell line chr17:40939700..40939701 29129909 RNA-Seq:(High) rs1332978941 Functional Loss SNV ICGC 33..33 33 PBCA 1 - 53019 RMVar_ID_53019 Human_SNP_ID_828248863 A-to-I Human chr17 + 62604144 62604144 62604144 CTCCTGCCTCAGCCTCTCAAGTAGCTGGGTTTACATGCACCCGCCACCACGCCCAGCTAATTTTT CTCCTGCCTCAGCCTCTCAAGTAGCTGGGTTTTCATGCACCCGCCACCACGCCCAGCTAATTTTT A T TLK2 Ensembl:ENSG00000146872 Protein coding intron GSE38233 cultured B-cells chr17:62604143..62604144 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 5 breast 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 53020 RMVar_ID_53020 Human_SNP_ID_828256461 A-to-I Human chr17 - 518680 518680 518680 TCACTGCAACCTCCGCCTCCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTGAGTATCGGATT TCACTGCAACCTCCGCCTCCCAGGTTCAAGCATTTCTCCTGCCTCAGCCTCCTGAGTATCGGATT T A VPS53 Ensembl:ENSG00000141252 Protein coding 3'UTR GSE100210 HepG2 cell line chr17:518679..518680 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_267135 53021 RMVar_ID_53021 Human_SNP_ID_828283492 A-to-I Human chr17 - 67338769 67338769 67338769 CGGCTCACTGCAACCTTTGCCTCCCATATTCAAGCAGTTCTCCTGCCTCAACCTCCCAAGTAGCT CGGCTCACTGCAACCTTTGCCTCCCATATTCACGCAGTTCTCCTGCCTCAACCTCCCAAGTAGCT T G PSMD12 Ensembl:ENSG00000197170 Protein coding 3'UTR GSE100210;GSE99789 HepG2 cell line;esophageal squamous carcinoma cells,EC109 chr17:67338768..67338769 29129909,29796672 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 53022 RMVar_ID_53022 Human_SNP_ID_828284056 A-to-I Human chr17 - 50761145 50761127 50761146 GTCCCAGCTACATGGGAAGCTGAGGCAGGAGAATCACCTGAACCCAGGAGGCAGAGGTTGCAGTG GTCCCAGCTACATGGGAAGCTGAGGCAGGAG___________________GCAGAGGTTGCAGTG CCTCCTGGGTTCAGGTGATT C ANKRD40CL Ensembl:ENSG00000167117 Protein coding exon GSE47997 K562 cells&HepG2 cells chr17:50761144..50761145 23474544 RNA-Seq:(High) - Functional Loss DEL ICGC 32..50 33 PAAD 1 - 53023 RMVar_ID_53023 Human_SNP_ID_828284431 A-to-I Human chr17 - 45152965 45152964 45152965 GGAGTGCAATGGCGCGATCTCCTCTCACTGCAACCTCCACCTCCCGGGTTCAAACGATTCTGCTG GGAGTGCAATGGCGCGATCTCCTCTCACTGCA_CCTCCACCTCCCGGGTTCAAACGATTCTGCTG GT G AC138150.1 Ensembl:ENSG00000224505 lincRNA intron GSE100210 HepG2 cell line chr17:45152964..45152965 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 33..33 33 MALY 1 - 53024 RMVar_ID_53024 Human_SNP_ID_828292423 A-to-I Human chr17 - 69293821 69293821 69293821 ACACACACACACACACACACCAGTATGATTGTAGGGTGGGGGATTAGGGGAGGTTTGTTTTAAGT ACACACACACACACACACACCAGTATGATTGTGGGGTGGGGGATTAGGGGAGGTTTGTTTTAAGT T C ABCA5 Ensembl:ENSG00000154265 Protein coding intron GSE100210 HepG2 cell line chr17:69293820..69293821 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - RMVar_hsa_circ_961,RMVar_hsa_circ_74010,RMVar_hsa_circ_59931,RMVar_hsa_circ_368471,RMVar_hsa_circ_57156,RMVar_hsa_circ_376221,RMVar_hsa_circ_186838,RMVar_hsa_circ_186839,RMVar_hsa_circ_1232,RMVar_hsa_circ_186840,RMVar_hsa_circ_11632,RMVar_hsa_circ_71431,RMVar_hsa_circ_16606,RMVar_hsa_circ_186843,RMVar_hsa_circ_329472,RMVar_hsa_circ_367993,RMVar_hsa_circ_186844,RMVar_hsa_circ_67714,RMVar_hsa_circ_61059,RMVar_hsa_circ_40158,RMVar_hsa_circ_6152,RMVar_hsa_circ_21108,RMVar_hsa_circ_363665,RMVar_hsa_circ_64458,RMVar_hsa_circ_266907,RMVar_hsa_circ_186849,RMVar_hsa_circ_58938,RMVar_hsa_circ_186850,RMVar_hsa_circ_285601,RMVar_hsa_circ_60103 53025 RMVar_ID_53025 Human_SNP_ID_828298621 A-to-I Human chr17 - 657201 657201 657201 GAGACCAAGTACAAGTTGTGCAAAGTGAGAAAAATCTTTGTGGGCACAAAAGGAATCCCTCATCT GAGACCAAGTACAAGTTGTGCAAAGTGAGAAAGATCTTTGTGGGCACAAAAGGAATCCCTCATCT T C RPS4XP17,VPS53 Ensembl:ENSG00000244097,Ensembl:ENSG00000141252 Pseudogene,Protein coding exon,intron GSE107867 ASD brains,frontal_cortex chr17:657200..657201 30559470 RNA-Seq:(High) rs879060493 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 12 haematopoietic and lymphoid tissue 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_180923,RMVar_hsa_circ_180922,RMVar_hsa_circ_180920 53026 RMVar_ID_53026 Human_SNP_ID_828303933 A-to-I Human chr17 - 2331040 2331039 2331040 TCTCCATGGGATCCTAAGGAAAACCTTCCTCAAGATTATGCTCGAATATTTCAGTTTCAGAACTT TCTCCATGGGATCCTAAGGAAAACCTTCCTCA_GATTATGCTCGAATATTTCAGTTTCAGAACTT CT C TSR1 Ensembl:ENSG00000167721 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector chr17:2331039..2331040 29967493 RNA-Seq:(High) - Functional Loss DEL TCGA 33..33 33 LUAD 1 - Human_RBP_ID_50830,Human_RBP_ID_1851246 Human_Splice_Rec_1759708,Human_Splice_Rec_1759709,Human_Splice_Rec_1759721 Human_miRNA_ID_1689493 RMVar_hsa_circ_269562,RMVar_hsa_circ_310108,RMVar_hsa_circ_315654 53027 RMVar_ID_53027 Human_SNP_ID_828304020 A-to-I Human chr17 + 27083529 27083529 27083529 CACATACACCACCACATGCTCCACCCCAATCTATTTGGCCAGTAATAAGTGCTCTCGGGTCTAGG CACATACACCACCACATGCTCCACCCCAATCTGTTTGGCCAGTAATAAGTGCTCTCGGGTCTAGG A G - - Other Unknown GSE100210 HepG2 cell line chr17:27083528..27083529 29129909 RNA-Seq:(High) rs878876452 Functional Loss SNV ICGC 33..33 33 LAML 1 - 53028 RMVar_ID_53028 Human_SNP_ID_828312221 A-to-I Human chr17 - 17224713 17224712 17224713 GCCAACATGGTGAAACCCCCTCTCTAAAAAAAATACAAAAAAATTAGCCAGGCGTGGTGGCACAC GCCAACATGGTGAAACCCCCTCTCTAAAAAAA_TACAAAAAAATTAGCCAGGCGTGGTGGCACAC AT A FLCN,AC055811.2 Ensembl:ENSG00000154803,Ensembl:ENSG00000264187 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells chr17:17224712..17224713 24183664 RNA-Seq:(High) rs533953146 Functional Loss DEL ICGC 33..33 33 ESCA 2 - RMVar_hsa_circ_2718,RMVar_hsa_circ_10993,RMVar_hsa_circ_108392,RMVar_hsa_circ_7049,RMVar_hsa_circ_28716,RMVar_hsa_circ_182386,RMVar_hsa_circ_367641,RMVar_hsa_circ_370906,RMVar_hsa_circ_334202,RMVar_hsa_circ_182385,RMVar_hsa_circ_182387 53029 RMVar_ID_53029 Human_SNP_ID_828318394 A-to-I Human chr17 + 40238638 40238634 40238638 TTTATTTATTTATTATTATTTTTTTGAGACAGAATCTCACTCTGTCGTCCAGGCTGGAGTGCAGT TTTATTTATTTATTATTATTTTTTTGAGA____ATCTCACTCTGTCGTCCAGGCTGGAGTGCAGT ACAGA A WIPF2 Ensembl:ENSG00000171475 Protein coding intron GSE100210 HepG2 cell line chr17:40238638..40238639 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 30..33 33 LMS 1 - 53030 RMVar_ID_53030 Human_SNP_ID_828355349 A-to-I Human chr17 - 39385994 39385994 39385994 TTGAGACGGAATCTCTGTTGTCAGGCTGGAGTACAGTGGCGCGATCTTGGCTGACTGCAACCTCT TTGAGACGGAATCTCTGTTGTCAGGCTGGAGTGCAGTGGCGCGATCTTGGCTGACTGCAACCTCT T C FBXL20 Ensembl:ENSG00000108306 Protein coding intron GSE100210 HepG2 cell line chr17:39385993..39385994 29129909 RNA-Seq:(High) rs1426080093 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 5 haematopoietic and lymphoid tissue Human_RBP_ID_1533001,Human_RBP_ID_12993053 53031 RMVar_ID_53031 Human_SNP_ID_828357991 A-to-I Human chr17 + 30787810 30787810 30787810 TCACCTGAGGTCAGGAGTTCCAAGACCACCCTAGGCAACATGGTGAAACCCCGTATCTACAAAAA TCACCTGAGGTCAGGAGTTCCAAGACCACCCTGGGCAACATGGTGAAACCCCGTATCTACAAAAA A G SUZ12P1 Ensembl:ENSG00000264538 Pseudogene intron GSE100210 HepG2 cell line chr17:30787809..30787810 29129909 RNA-Seq:(High) rs1370595194 Functional Loss SNV ICGC 33..33 33 MALY 1 - RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247 53032 RMVar_ID_53032 Human_SNP_ID_828360319 A-to-I Human chr17 + 82002992 82002992 82002992 CACCTCCTGGGTTCAAGCGATTTTCGTGTCTCAGCCTCCTGAATAGCTGGGATTACAGGTGCCCG CACCTCCTGGGTTCAAGCGATTTTCGTGTCTCTGCCTCCTGAATAGCTGGGATTACAGGTGCCCG A T ASPSCR1 Ensembl:ENSG00000169696 Protein coding intron GSE100210 HepG2 cell line chr17:82002991..82002992 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LMS 1 - Human_RBP_ID_17567153 RMVar_hsa_circ_56317,RMVar_hsa_circ_27983,RMVar_hsa_circ_55539 53033 RMVar_ID_53033 Human_SNP_ID_828360622 A-to-I Human chr17 - 19902933 19902933 19902933 ACATCTCTGCACTCCAGCCTGGGCAACAGAGCAAGACTCTGTCTCAAAAAAAAAAGAATTTGGCC ACATCTCTGCACTCCAGCCTGGGCAACAGAGCCAGACTCTGTCTCAAAAAAAAAAGAATTTGGCC T G - - Other Unknown GSE100210 HepG2 cell line chr17:19902932..19902933 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - 53034 RMVar_ID_53034 Human_SNP_ID_828363490 A-to-I Human chr17 + 63831937 63831937 63831937 CCCACCCCTAGGTCATGCAGAAGGACAGTGAGAAAAACATGTCCATCAAGAAATTATGGAAGTGA CCCACCCCTAGGTCATGCAGAAGGACAGTGAGGAAAACATGTCCATCAAGAAATTATGGAAGTGA A G PSMC5 Ensembl:ENSG00000087191 Protein coding CDS GSE100210 HepG2 cell line chr17:63831937..63831938 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_1540056,Human_RBP_ID_1866880,Human_RBP_ID_26812690 Human_Splice_Rec_1853656,Human_Splice_Rec_1853742,Human_Splice_Rec_1853766,Human_Splice_Rec_1853798,Human_Splice_Rec_1853820,Human_Splice_Rec_1853842,Human_Splice_Rec_1853864,Human_Splice_Rec_1853888 RMVar_hsa_circ_98129,RMVar_hsa_circ_86525,RMVar_hsa_circ_186378,RMVar_hsa_circ_186381,RMVar_hsa_circ_114832,RMVar_hsa_circ_186382 53035 RMVar_ID_53035 Human_SNP_ID_828374907 A-to-I Human chr17 - 69252715 69252715 69252715 CTCCTGCCTCAGCCTTCCAAGTACCTGGGACTACAGGCAAGAGCCACCAAGCCCGGCTAATTTTT CTCCTGCCTCAGCCTTCCAAGTACCTGGGACTGCAGGCAAGAGCCACCAAGCCCGGCTAATTTTT T C ABCA5 Ensembl:ENSG00000154265 Protein coding intron GSE100210 HepG2 cell line chr17:69252714..69252715 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 3 pancreas RMVar_hsa_circ_74010,RMVar_hsa_circ_368768,RMVar_hsa_circ_59931 53036 RMVar_ID_53036 Human_SNP_ID_828377291 A-to-I Human chr17 + 34256846 34256846 34256846 CTCCGAAGACTTGAACACTCACTCCACAACCCAAGAATCTGCAGCTAACTTATTTTCCCCTAGCT CTCCGAAGACTTGAACACTCACTCCACAACCCTAGAATCTGCAGCTAACTTATTTTCCCCTAGCT A T CCL2 Ensembl:ENSG00000108691 Protein coding 3'UTR GSE100210 HepG2 cell line chr17:34256846..34256847 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 2 head and neck 53037 RMVar_ID_53037 Human_SNP_ID_828384424 A-to-I Human chr17 - 38849513 38849513 38849513 ACCAACGTGGTGAAACCTCCTCTTTTCTAAAAATACAAAAATTAGCTGGGCGTGGTGGCGCACCG ACCAACGTGGTGAAACCTCCTCTTTTCTAAAAGTACAAAAATTAGCTGGGCGTGGTGGCGCACCG T C RPL23 Ensembl:ENSG00000125691 Protein coding 3'UTR GSE100210 HepG2 cell line chr17:38849512..38849513 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_25278844 53038 RMVar_ID_53038 Human_SNP_ID_828400856 A-to-I Human chr17 - 31862039 31862039 31862039 CACCCGCCTTGGCCTCCCAAAGTGTTGGGATTACAGGCGTGAACCACTAAGCCTGGCCTGGACTG CACCCGCCTTGGCCTCCCAAAGTGTTGGGATTCCAGGCGTGAACCACTAAGCCTGGCCTGGACTG T G UTP6 Ensembl:ENSG00000108651 Protein coding 3'UTR GSE100210 HepG2 cell line chr17:31862038..31862039 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_12962776 53039 RMVar_ID_53039 Human_SNP_ID_828404441 A-to-I Human chr17 - 1704948 1704948 1704948 CCTGTAATCCCAGCATTTTGGGAGGCCGAGGCAGGCGGATCACGAGGTCAGGAGATGACCATCCT CCTGTAATCCCAGCATTTTGGGAGGCCGAGGCGGGCGGATCACGAGGTCAGGAGATGACCATCCT T C TLCD2 Ensembl:ENSG00000185561 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line chr17:1704947..1704948 31158229 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LMS 1 - 53040 RMVar_ID_53040 Human_SNP_ID_828405282 A-to-I Human chr17 + 32450976 32450976 32450976 ACCACATATCTACAAAAAAGATAAAAAAATTGACTGGGTGTGGTGGTGCGTGCCTGTGTCCCAGG ACCACATATCTACAAAAAAGATAAAAAAATTGGCTGGGTGTGGTGGTGCGTGCCTGTGTCCCAGG A G PSMD11 Ensembl:ENSG00000108671 Protein coding intron GSE100210 HepG2 cell line chr17:32450975..32450976 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_6583258 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_183547,RMVar_hsa_circ_291310,RMVar_hsa_circ_183546,RMVar_hsa_circ_183543,RMVar_hsa_circ_183544 53041 RMVar_ID_53041 Human_SNP_ID_828419963 A-to-I Human chr17 - 62007592 62007592 62007592 CGCCCGCCTCGGCCTCCTAAAGTGCTGGGATTACAGGCGTGAACCACCACGCCCGGCCAAGGTCT CGCCCGCCTCGGCCTCCTAAAGTGCTGGGATTTCAGGCGTGAACCACCACGCCCGGCCAAGGTCT T A MED13 Ensembl:ENSG00000108510 Protein coding intron GSE38233 cultured B-cells chr17:62007591..62007592 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_10550,RMVar_hsa_circ_85045,RMVar_hsa_circ_104817,RMVar_hsa_circ_186111,RMVar_hsa_circ_119612,RMVar_hsa_circ_81309,RMVar_hsa_circ_110787,RMVar_hsa_circ_102026,RMVar_hsa_circ_186123,RMVar_hsa_circ_186124,RMVar_hsa_circ_186122,RMVar_hsa_circ_88424,RMVar_hsa_circ_186125,RMVar_hsa_circ_186126,RMVar_hsa_circ_83249,RMVar_hsa_circ_186127,RMVar_hsa_circ_120621,RMVar_hsa_circ_186133,RMVar_hsa_circ_101240,RMVar_hsa_circ_121360,RMVar_hsa_circ_50231,RMVar_hsa_circ_186138,RMVar_hsa_circ_186139,RMVar_hsa_circ_186140,RMVar_hsa_circ_89268,RMVar_hsa_circ_186142,RMVar_hsa_circ_372759,RMVar_hsa_circ_104772,RMVar_hsa_circ_186143,RMVar_hsa_circ_186144,RMVar_hsa_circ_353824,RMVar_hsa_circ_361895,RMVar_hsa_circ_62540,RMVar_hsa_circ_123911,RMVar_hsa_circ_186152,RMVar_hsa_circ_336303,RMVar_hsa_circ_120286,RMVar_hsa_circ_186155,RMVar_hsa_circ_304263,RMVar_hsa_circ_279047,RMVar_hsa_circ_290568,RMVar_hsa_circ_355612,RMVar_hsa_circ_96938,RMVar_hsa_circ_186159,RMVar_hsa_circ_22555,RMVar_hsa_circ_298747,RMVar_hsa_circ_186158,RMVar_hsa_circ_284367,RMVar_hsa_circ_186162 53042 RMVar_ID_53042 Human_SNP_ID_828426142 A-to-I Human chr17 - 2116479 2116479 2116479 AACTCCTGACCCCACCCACCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCATGCC AACTCCTGACCCCACCCACCTCAGCCTCCCAACGTGCTGGGATTACAGGCGTGAGCCACCATGCC T G SMG6 Ensembl:ENSG00000070366 Protein coding intron GSE100210 HepG2 cell line chr17:2116478..2116479 29129909 RNA-Seq:(High) rs1007172907 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 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_181201,RMVar_hsa_circ_119218,RMVar_hsa_circ_181203,RMVar_hsa_circ_76780,RMVar_hsa_circ_181204 53043 RMVar_ID_53043 Human_SNP_ID_828431783 A-to-I Human chr17 + 59201707 59201707 59201707 AGATAAAAACACCCAGCTGGGTGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAG AGATAAAAACACCCAGCTGGGTGCAGTGGCTCTCACCTGTAATCCCAGCACTTTGGGAGGCTGAG A T AC099850.3,PRR11 Ensembl:ENSG00000265303,Ensembl:ENSG00000068489 Protein coding,Protein coding intron,3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line chr17:59201706..59201707 29129909,31158229 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus Human_Splice_Rec_1847035,Human_Splice_Rec_1847077,Human_Splice_Rec_1847097 Human_miRNA_ID_1943418,Human_miRNA_ID_2117609,Human_miRNA_ID_2201191,Human_miRNA_ID_2204254,Human_miRNA_ID_2316800,Human_miRNA_ID_2319953,Human_miRNA_ID_2326286,Human_miRNA_ID_2520663,Human_miRNA_ID_2523829,Human_miRNA_ID_2775646,Human_miRNA_ID_2823014,Human_miRNA_ID_2836426,Human_miRNA_ID_2846827,Human_miRNA_ID_2891094,Human_miRNA_ID_3113703 RMVar_hsa_circ_97892,RMVar_hsa_circ_185763 53044 RMVar_ID_53044 Human_SNP_ID_828453281 A-to-I Human chr17 - 81284313 81284313 81284313 GAGTTTTGCTCTGTCACCCAGGCTGGAGTGCAATGCTGTGATCTCGGCTCACTGCAACCTCCCAG GAGTTTTGCTCTGTCACCCAGGCTGGAGTGCAGTGCTGTGATCTCGGCTCACTGCAACCTCCCAG T C SLC38A10 Ensembl:ENSG00000157637 Protein coding intron GSE38233 cultured B-cells chr17:81284312..81284313 24183664 RNA-Seq:(High) rs558207205 Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 5 pancreas RMVar_hsa_circ_125038,RMVar_hsa_circ_76394,RMVar_hsa_circ_187598,RMVar_hsa_circ_125698,RMVar_hsa_circ_187601,RMVar_hsa_circ_340994,RMVar_hsa_circ_290228,RMVar_hsa_circ_339696,RMVar_hsa_circ_187606,RMVar_hsa_circ_187605,RMVar_hsa_circ_47429,RMVar_hsa_circ_108875,RMVar_hsa_circ_283359,RMVar_hsa_circ_278595,RMVar_hsa_circ_187614,RMVar_hsa_circ_187613,RMVar_hsa_circ_187621,RMVar_hsa_circ_272150,RMVar_hsa_circ_187623,RMVar_hsa_circ_36091 53045 RMVar_ID_53045 Human_SNP_ID_828483211 A-to-I Human chr17 - 54959892 54959892 54959892 AAATATTAGGACAAGTGCAGTGGCTCACACCTATAATCCCAGCACTCTGGGAGGCTGAGGTGGGT AAATATTAGGACAAGTGCAGTGGCTCACACCTGTAATCCCAGCACTCTGGGAGGCTGAGGTGGGT T C COX11 Ensembl:ENSG00000166260 Protein coding intron GSE100210 HepG2 cell line chr17:54959891..54959892 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 5 prostate Human_RBP_ID_25302475 53046 RMVar_ID_53046 Human_SNP_ID_828497870 A-to-I Human chr17 - 16381931 16381931 16381931 GGCTCCACCTCAAGGGTGATGGTCTTGCCGGTAAGGGTTTTCACGAAGATCTGCATTTTGACCTA GGCTCCACCTCAAGGGTGATGGTCTTGCCGGTCAGGGTTTTCACGAAGATCTGCATTTTGACCTA T G - - Other Unknown GSE107867 ASD brains,cerebellum;ASD brains,frontal_cortex chr17:16381930..16381931 30559470 RNA-Seq:(High) rs542187113 Functional Loss SNV COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 5 brain 53047 RMVar_ID_53047 Human_SNP_ID_828526498 A-to-I Human chr17 - 47082146 47082146 47082146 TCCATGTTGTTCATGTTGGTTTCGAACTCCCAACCTCAGGTGATCTGCCTGCCTCCGCCTCCCAA TCCATGTTGTTCATGTTGGTTTCGAACTCCCAGCCTCAGGTGATCTGCCTGCCTCCGCCTCCCAA T C AC005670.3 Ensembl:ENSG00000262879 lincRNA intron GSE100210 HepG2 cell line chr17:47082145..47082146 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LMS 1 - Human_RBP_ID_491735,Human_RBP_ID_13044096 53048 RMVar_ID_53048 Human_SNP_ID_828536820 A-to-I Human chr17 - 16160599 16160599 16160599 TTTAATAAAGCAGGAATTTCACCATGTTGGCTAGGCTGGTCTTGAACTCCTGGGCTCAAGTGATC TTTAATAAAGCAGGAATTTCACCATGTTGGCTTGGCTGGTCTTGAACTCCTGGGCTCAAGTGATC T A NCOR1 Ensembl:ENSG00000141027 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr17:16160598..16160599 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 5 liver RMVar_hsa_circ_79163,RMVar_hsa_circ_182246,RMVar_hsa_circ_98921,RMVar_hsa_circ_123782,RMVar_hsa_circ_182261,RMVar_hsa_circ_182262,RMVar_hsa_circ_96187,RMVar_hsa_circ_182270,RMVar_hsa_circ_85654,RMVar_hsa_circ_182275,RMVar_hsa_circ_23603,RMVar_hsa_circ_17899,RMVar_hsa_circ_119362,RMVar_hsa_circ_182284,RMVar_hsa_circ_40412,RMVar_hsa_circ_353205,RMVar_hsa_circ_44380,RMVar_hsa_circ_264849,RMVar_hsa_circ_182289,RMVar_hsa_circ_292653,RMVar_hsa_circ_339704,RMVar_hsa_circ_333668,RMVar_hsa_circ_84455,RMVar_hsa_circ_182291,RMVar_hsa_circ_182292,RMVar_hsa_circ_321833,RMVar_hsa_circ_87362,RMVar_hsa_circ_81717,RMVar_hsa_circ_182300,RMVar_hsa_circ_315517,RMVar_hsa_circ_290358,RMVar_hsa_circ_182302,RMVar_hsa_circ_182303,RMVar_hsa_circ_351158,RMVar_hsa_circ_52472,RMVar_hsa_circ_182304,RMVar_hsa_circ_182306,RMVar_hsa_circ_182308,RMVar_hsa_circ_289128,RMVar_hsa_circ_182305,RMVar_hsa_circ_299165,RMVar_hsa_circ_277957,RMVar_hsa_circ_182307 53049 RMVar_ID_53049 Human_SNP_ID_828550274 A-to-I Human chr17 - 75284240 75284240 75284240 CGCCACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTCCACCATATTGGCCAGGC CGCCACCATGCCTGGCTAATTTTTGTATTTTTGGTAGAGACAGGGTTCCACCATATTGGCCAGGC T C SLC25A19 Ensembl:ENSG00000125454 Protein coding intron GSE38233 cultured B-cells chr17:75284239..75284240 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_41815,RMVar_hsa_circ_352087,RMVar_hsa_circ_300175 53050 RMVar_ID_53050 Human_SNP_ID_828561317 A-to-I Human chr17 + 30781082 30781082 30781082 CTGACTGCAGCCTCCACCCCCCGAGTTCAAGCAATTCTCCTGCCTCAGCCTCCCATGTGGCTGGG CTGACTGCAGCCTCCACCCCCCGAGTTCAAGCGATTCTCCTGCCTCAGCCTCCCATGTGGCTGGG A G SUZ12P1 Ensembl:ENSG00000264538 Pseudogene intron GSE100210 HepG2 cell line chr17:30781082..30781083 29129909 RNA-Seq:(High) rs72811650 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_12956572 GWAS_ID_6151,GWAS_ID_6152,GWAS_ID_6153,GWAS_ID_6154,GWAS_ID_6155,GWAS_ID_6156,GWAS_ID_6157,GWAS_ID_6158,GWAS_ID_6159,GWAS_ID_6160,GWAS_ID_6161,GWAS_ID_6162,GWAS_ID_6163,GWAS_ID_6164,GWAS_ID_6165,GWAS_ID_6166,GWAS_ID_6167,GWAS_ID_6168,GWAS_ID_6169,GWAS_ID_6170,GWAS_ID_6171,GWAS_ID_6172,GWAS_ID_6173,GWAS_ID_6174,GWAS_ID_6175,GWAS_ID_6176,GWAS_ID_6177,GWAS_ID_6178,GWAS_ID_6179,GWAS_ID_6180,GWAS_ID_6181,GWAS_ID_6182,GWAS_ID_6183,GWAS_ID_6184,GWAS_ID_6185,GWAS_ID_6186,GWAS_ID_6187,GWAS_ID_6188,GWAS_ID_6189,GWAS_ID_6190,GWAS_ID_6191,GWAS_ID_6192,GWAS_ID_6193,GWAS_ID_6194,GWAS_ID_6195,GWAS_ID_6196,GWAS_ID_6197,GWAS_ID_6198,GWAS_ID_6199,GWAS_ID_6200,GWAS_ID_6201,GWAS_ID_6202,GWAS_ID_6203,GWAS_ID_6204,GWAS_ID_6205,GWAS_ID_6206,GWAS_ID_6207,GWAS_ID_6208,GWAS_ID_6209,GWAS_ID_6210,GWAS_ID_6211,GWAS_ID_6212,GWAS_ID_6213,GWAS_ID_6214,GWAS_ID_6215,GWAS_ID_6216,GWAS_ID_6217,GWAS_ID_6218,GWAS_ID_6219,GWAS_ID_6220,GWAS_ID_6221,GWAS_ID_6222,GWAS_ID_6223,GWAS_ID_6224,GWAS_ID_6225,GWAS_ID_6226,GWAS_ID_6227,GWAS_ID_6228,GWAS_ID_6229,GWAS_ID_6230,GWAS_ID_6231,GWAS_ID_6232,GWAS_ID_6233,GWAS_ID_6234,GWAS_ID_6235,GWAS_ID_6236,GWAS_ID_6237,GWAS_ID_6238,GWAS_ID_6239,GWAS_ID_6240,GWAS_ID_6241,GWAS_ID_6242,GWAS_ID_6243,GWAS_ID_6244,GWAS_ID_6245,GWAS_ID_6246,GWAS_ID_6247,GWAS_ID_6248,GWAS_ID_6249,GWAS_ID_6250,GWAS_ID_6251,GWAS_ID_6252,GWAS_ID_6253,GWAS_ID_6254,GWAS_ID_6255,GWAS_ID_6256,GWAS_ID_6257,GWAS_ID_6258,GWAS_ID_6259,GWAS_ID_6260,GWAS_ID_6261,GWAS_ID_6262,GWAS_ID_6263,GWAS_ID_6264,GWAS_ID_6265,GWAS_ID_6266,GWAS_ID_6267,GWAS_ID_6268,GWAS_ID_6269,GWAS_ID_6270,GWAS_ID_6271,GWAS_ID_6272,GWAS_ID_6273,GWAS_ID_6274,GWAS_ID_6275,GWAS_ID_6276,GWAS_ID_6277,GWAS_ID_6278,GWAS_ID_6279,GWAS_ID_6280,GWAS_ID_6281,GWAS_ID_6282,GWAS_ID_6283,GWAS_ID_6284,GWAS_ID_6285,GWAS_ID_6286,GWAS_ID_6287,GWAS_ID_6288,GWAS_ID_6289,GWAS_ID_6290,GWAS_ID_6291,GWAS_ID_6292,GWAS_ID_6293,GWAS_ID_6294,GWAS_ID_6295,GWAS_ID_6296,GWAS_ID_6297,GWAS_ID_6298,GWAS_ID_6299,GWAS_ID_6300,GWAS_ID_6301,GWAS_ID_6302,GWAS_ID_6303,GWAS_ID_6304,GWAS_ID_6305,GWAS_ID_6306,GWAS_ID_6307,GWAS_ID_6308,GWAS_ID_6309,GWAS_ID_6310,GWAS_ID_6311,GWAS_ID_6312,GWAS_ID_6313,GWAS_ID_6314,GWAS_ID_6315,GWAS_ID_6316,GWAS_ID_6317,GWAS_ID_6318,GWAS_ID_6319,GWAS_ID_6320,GWAS_ID_6321,GWAS_ID_6322,GWAS_ID_6323,GWAS_ID_6324,GWAS_ID_6325,GWAS_ID_6326,GWAS_ID_6327 RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_293925,RMVar_hsa_circ_183261,RMVar_hsa_circ_68200,RMVar_hsa_circ_183260 53051 RMVar_ID_53051 Human_SNP_ID_828561365 A-to-I Human chr17 + 30781082 30781082 30781082 CTGACTGCAGCCTCCACCCCCCGAGTTCAAGCAATTCTCCTGCCTCAGCCTCCCATGTGGCTGGG CTGACTGCAGCCTCCACCCCCCGAGTTCAAGCCATTCTCCTGCCTCAGCCTCCCATGTGGCTGGG A C SUZ12P1 Ensembl:ENSG00000264538 Pseudogene intron GSE100210 HepG2 cell line chr17:30781082..30781083 29129909 RNA-Seq:(High) rs72811650 Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_12956572 GWAS_ID_6151,GWAS_ID_6152,GWAS_ID_6153,GWAS_ID_6154,GWAS_ID_6155,GWAS_ID_6156,GWAS_ID_6157,GWAS_ID_6158,GWAS_ID_6159,GWAS_ID_6160,GWAS_ID_6161,GWAS_ID_6162,GWAS_ID_6163,GWAS_ID_6164,GWAS_ID_6165,GWAS_ID_6166,GWAS_ID_6167,GWAS_ID_6168,GWAS_ID_6169,GWAS_ID_6170,GWAS_ID_6171,GWAS_ID_6172,GWAS_ID_6173,GWAS_ID_6174,GWAS_ID_6175,GWAS_ID_6176,GWAS_ID_6177,GWAS_ID_6178,GWAS_ID_6179,GWAS_ID_6180,GWAS_ID_6181,GWAS_ID_6182,GWAS_ID_6183,GWAS_ID_6184,GWAS_ID_6185,GWAS_ID_6186,GWAS_ID_6187,GWAS_ID_6188,GWAS_ID_6189,GWAS_ID_6190,GWAS_ID_6191,GWAS_ID_6192,GWAS_ID_6193,GWAS_ID_6194,GWAS_ID_6195,GWAS_ID_6196,GWAS_ID_6197,GWAS_ID_6198,GWAS_ID_6199,GWAS_ID_6200,GWAS_ID_6201,GWAS_ID_6202,GWAS_ID_6203,GWAS_ID_6204,GWAS_ID_6205,GWAS_ID_6206,GWAS_ID_6207,GWAS_ID_6208,GWAS_ID_6209,GWAS_ID_6210,GWAS_ID_6211,GWAS_ID_6212,GWAS_ID_6213,GWAS_ID_6214,GWAS_ID_6215,GWAS_ID_6216,GWAS_ID_6217,GWAS_ID_6218,GWAS_ID_6219,GWAS_ID_6220,GWAS_ID_6221,GWAS_ID_6222,GWAS_ID_6223,GWAS_ID_6224,GWAS_ID_6225,GWAS_ID_6226,GWAS_ID_6227,GWAS_ID_6228,GWAS_ID_6229,GWAS_ID_6230,GWAS_ID_6231,GWAS_ID_6232,GWAS_ID_6233,GWAS_ID_6234,GWAS_ID_6235,GWAS_ID_6236,GWAS_ID_6237,GWAS_ID_6238,GWAS_ID_6239,GWAS_ID_6240,GWAS_ID_6241,GWAS_ID_6242,GWAS_ID_6243,GWAS_ID_6244,GWAS_ID_6245,GWAS_ID_6246,GWAS_ID_6247,GWAS_ID_6248,GWAS_ID_6249,GWAS_ID_6250,GWAS_ID_6251,GWAS_ID_6252,GWAS_ID_6253,GWAS_ID_6254,GWAS_ID_6255,GWAS_ID_6256,GWAS_ID_6257,GWAS_ID_6258,GWAS_ID_6259,GWAS_ID_6260,GWAS_ID_6261,GWAS_ID_6262,GWAS_ID_6263,GWAS_ID_6264,GWAS_ID_6265,GWAS_ID_6266,GWAS_ID_6267,GWAS_ID_6268,GWAS_ID_6269,GWAS_ID_6270,GWAS_ID_6271,GWAS_ID_6272,GWAS_ID_6273,GWAS_ID_6274,GWAS_ID_6275,GWAS_ID_6276,GWAS_ID_6277,GWAS_ID_6278,GWAS_ID_6279,GWAS_ID_6280,GWAS_ID_6281,GWAS_ID_6282,GWAS_ID_6283,GWAS_ID_6284,GWAS_ID_6285,GWAS_ID_6286,GWAS_ID_6287,GWAS_ID_6288,GWAS_ID_6289,GWAS_ID_6290,GWAS_ID_6291,GWAS_ID_6292,GWAS_ID_6293,GWAS_ID_6294,GWAS_ID_6295,GWAS_ID_6296,GWAS_ID_6297,GWAS_ID_6298,GWAS_ID_6299,GWAS_ID_6300,GWAS_ID_6301,GWAS_ID_6302,GWAS_ID_6303,GWAS_ID_6304,GWAS_ID_6305,GWAS_ID_6306,GWAS_ID_6307,GWAS_ID_6308,GWAS_ID_6309,GWAS_ID_6310,GWAS_ID_6311,GWAS_ID_6312,GWAS_ID_6313,GWAS_ID_6314,GWAS_ID_6315,GWAS_ID_6316,GWAS_ID_6317,GWAS_ID_6318,GWAS_ID_6319,GWAS_ID_6320,GWAS_ID_6321,GWAS_ID_6322,GWAS_ID_6323,GWAS_ID_6324,GWAS_ID_6325,GWAS_ID_6326,GWAS_ID_6327 RMVar_hsa_circ_121158,RMVar_hsa_circ_183246,RMVar_hsa_circ_126791,RMVar_hsa_circ_183247,RMVar_hsa_circ_293925,RMVar_hsa_circ_183261,RMVar_hsa_circ_68200,RMVar_hsa_circ_183260 53052 RMVar_ID_53052 Human_SNP_ID_828565235 A-to-I Human chr17 + 59827462 59827462 59827462 CCTCAGCCTCCCAAGCAGCTAAGACTACAGGCATGCACCACCACCCCCAGCTAATTTTTGTATTT CCTCAGCCTCCCAAGCAGCTAAGACTACAGGCGTGCACCACCACCCCCAGCTAATTTTTGTATTT A G VMP1 Ensembl:ENSG00000062716 Protein coding intron GSE38233 cultured B-cells chr17:59827461..59827462 24183664 RNA-Seq:(High) rs2526352 Functional Loss SNV ICGC 33..33 33 LAML 1 - RMVar_hsa_circ_102889,RMVar_hsa_circ_185825,RMVar_hsa_circ_87762,RMVar_hsa_circ_185835,RMVar_hsa_circ_185844,RMVar_hsa_circ_336973,RMVar_hsa_circ_79913,RMVar_hsa_circ_79474,RMVar_hsa_circ_88941,RMVar_hsa_circ_185853,RMVar_hsa_circ_185854,RMVar_hsa_circ_120271,RMVar_hsa_circ_185860,RMVar_hsa_circ_92862,RMVar_hsa_circ_185859 53053 RMVar_ID_53053 Human_SNP_ID_828596490 A-to-I Human chr17 + 37428630 37428630 37428630 TTGAGACAGGGTCTCACTCTATCACCCAGGCTAAAGAGCAGTGGCACAATCACAGCTCACTGTAA TTGAGACAGGGTCTCACTCTATCACCCAGGCTGAAGAGCAGTGGCACAATCACAGCTCACTGTAA A G TADA2A Ensembl:ENSG00000276234 Protein coding intron GSE100210 HepG2 cell line chr17:37428629..37428630 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_306468,RMVar_hsa_circ_314366,RMVar_hsa_circ_57152,RMVar_hsa_circ_18670,RMVar_hsa_circ_323033,RMVar_hsa_circ_26784 53054 RMVar_ID_53054 Human_SNP_ID_828599500 A-to-I Human chr17 + 64468347 64468347 64468347 GTCTCACTCTGTTGCCCAGGCTGGAGTTCAGTAGCGCGATCTTGGCTCACTTCAATCTCCATCTT GTCTCACTCTGTTGCCCAGGCTGGAGTTCAGTGGCGCGATCTTGGCTCACTTCAATCTCCATCTT A G MILR1 Ensembl:ENSG00000271605 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line chr17:64468346..64468347 31158229 RNA-Seq:(High) rs1296240603 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue Human_Splice_Rec_1854872,Human_Splice_Rec_1854920 53055 RMVar_ID_53055 Human_SNP_ID_828600021 A-to-I Human chr17 - 1382561 1382561 1382561 GGTCAGGAGATTGAGATCATCCTGGCTAACATAGTGAAACCCCGTCTCTACTAAAGATACAAAAA GGTCAGGAGATTGAGATCATCCTGGCTAACATGGTGAAACCCCGTCTCTACTAAAGATACAAAAA T C YWHAE Ensembl:ENSG00000108953 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr17:1382560..1382561 24183664,29129909 RNA-Seq:(High) rs1471630803 Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_93985,RMVar_hsa_circ_180978,RMVar_hsa_circ_96697,RMVar_hsa_circ_180983 53056 RMVar_ID_53056 Human_SNP_ID_828600366 A-to-I Human chr17 - 7225399 7225399 7225399 TGGGAGATTTGGGCCATGTAGCTGCCTTTGTTACTCTATTTATTTTAGTCACTTGTATAAAACAC TGGGAGATTTGGGCCATGTAGCTGCCTTTGTTGCTCTATTTATTTTAGTCACTTGTATAAAACAC T C DVL2 Ensembl:ENSG00000004975 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector chr17:7225398..7225399 29967493 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_498831,Human_RBP_ID_1541357,Human_RBP_ID_1868626,Human_RBP_ID_3536652,Human_RBP_ID_5318852,Human_RBP_ID_6641701,Human_RBP_ID_8462304,Human_RBP_ID_13154212,Human_RBP_ID_18164607,Human_RBP_ID_22956914,Human_RBP_ID_24480948 Human_miRNA_ID_480372,Human_miRNA_ID_822945,Human_miRNA_ID_1760900,Human_miRNA_ID_2350643,Human_miRNA_ID_3084682 RMVar_hsa_circ_80217,RMVar_hsa_circ_181765 53057 RMVar_ID_53057 Human_SNP_ID_828658741 A-to-I Human chr17 + 82488066 82488066 82488066 ACACGTGCAGGAGCTGTACCAGGAGTGGCTGGAGGGGATCAACTCCCCCAAGGCCCGAGAGGTGC ACACGTGCAGGAGCTGTACCAGGAGTGGCTGGGGGGGATCAACTCCCCCAAGGCCCGAGAGGTGC A G NARF Ensembl:ENSG00000141562 Protein coding CDS GSE100210 HepG2 cell line chr17:82488065..82488066 29129909 RNA-Seq:(High) rs200355609 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,pancreas ductal_carcinoma,THCA,oesophagus squamous_cell_carcinoma,head_neck squamous_cell_carcinoma,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 39 oesophagus,pancreas,head and neck,haematopoietic and lymphoid tissue Human_RBP_ID_503669,Human_RBP_ID_5115003,Human_RBP_ID_5143425,Human_RBP_ID_9289580,Human_RBP_ID_17653712,Human_RBP_ID_17903460,Human_RBP_ID_18164100,Human_RBP_ID_22443282,Human_RBP_ID_27459576 53058 RMVar_ID_53058 Human_SNP_ID_828675605 A-to-I Human chr17 - 529929 529929 529929 GGGCTCAAGCCATCCTCCTGCCTCAACTTCTCAAGTATCTGGGACTACAGGAATGTACTACCATG GGGCTCAAGCCATCCTCCTGCCTCAACTTCTCTAGTATCTGGGACTACAGGAATGTACTACCATG T A VPS53 Ensembl:ENSG00000141252 Protein coding intron GSE100210 HepG2 cell line chr17:529928..529929 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - RMVar_hsa_circ_267135,RMVar_hsa_circ_42067,RMVar_hsa_circ_105613,RMVar_hsa_circ_75254,RMVar_hsa_circ_180893 53059 RMVar_ID_53059 Human_SNP_ID_828709623 A-to-I Human chr17 - 18306492 18306492 18306492 CATGGTGATGTATGCCTATAGTCCCAGCTACTAGTAAGGCTGAGGAAGGAGGATTACTTGATCCC CATGGTGATGTATGCCTATAGTCCCAGCTACTTGTAAGGCTGAGGAAGGAGGATTACTTGATCCC T A TOP3A Ensembl:ENSG00000177302 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr17:18306491..18306492 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - RMVar_hsa_circ_1055,RMVar_hsa_circ_36910,RMVar_hsa_circ_312192,RMVar_hsa_circ_117220,RMVar_hsa_circ_54695,RMVar_hsa_circ_53291,RMVar_hsa_circ_182501,RMVar_hsa_circ_182500,RMVar_hsa_circ_64243,RMVar_hsa_circ_182505,RMVar_hsa_circ_317353,RMVar_hsa_circ_182507,RMVar_hsa_circ_273006,RMVar_hsa_circ_47256,RMVar_hsa_circ_182508,RMVar_hsa_circ_291093,RMVar_hsa_circ_328604,RMVar_hsa_circ_182510,RMVar_hsa_circ_182512,RMVar_hsa_circ_318957,RMVar_hsa_circ_182513,RMVar_hsa_circ_329934,RMVar_hsa_circ_49377,RMVar_hsa_circ_288754 53060 RMVar_ID_53060 Human_SNP_ID_828732903 A-to-I Human chr17 - 44869517 44869517 44869517 AAGTAGAGGATCACTTGAGGCCAGGAGTTCAAAACCAGCCTAGGCAACATGGCAAGACCTCGTCT AAGTAGAGGATCACTTGAGGCCAGGAGTTCAACACCAGCCTAGGCAACATGGCAAGACCTCGTCT T G EFTUD2 Ensembl:ENSG00000108883 Protein coding intron GSE47997 K562 cells&HepG2 cells chr17:44869516..44869517 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_22586190 RMVar_hsa_circ_124097,RMVar_hsa_circ_108244,RMVar_hsa_circ_184740,RMVar_hsa_circ_184741,RMVar_hsa_circ_68804,RMVar_hsa_circ_103149,RMVar_hsa_circ_265863,RMVar_hsa_circ_113326,RMVar_hsa_circ_31587,RMVar_hsa_circ_184745,RMVar_hsa_circ_184744,RMVar_hsa_circ_184746,RMVar_hsa_circ_283264,RMVar_hsa_circ_82598,RMVar_hsa_circ_101650,RMVar_hsa_circ_367910,RMVar_hsa_circ_302184,RMVar_hsa_circ_184749,RMVar_hsa_circ_184750 53061 RMVar_ID_53061 Human_SNP_ID_828733657 A-to-I Human chr17 - 17213536 17213536 17213536 AACTGCTGGAAGGAGCTGTGTCCCAGCAAGGAAGGGAAACCATCAGGGCTGGGCTCGGCCCTGTC AACTGCTGGAAGGAGCTGTGTCCCAGCAAGGAGGGGAAACCATCAGGGCTGGGCTCGGCCCTGTC T C FLCN,AC055811.2 Ensembl:ENSG00000154803,Ensembl:ENSG00000264187 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line chr17:17213535..17213536 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA 33..33 33 OV 1 - 53062 RMVar_ID_53062 Human_SNP_ID_828737441 A-to-I Human chr17 - 18271896 18271896 18271896 ACACCCAGCTAATTTGTTTAGTATTTTTAGTAAAGACGGGGTTTCACCATGTTGGCCAGGCTGGT ACACCCAGCTAATTTGTTTAGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGGT T C TOP3A Ensembl:ENSG00000177302 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr17:18271895..18271896 24183664,29129909 RNA-Seq:(High) rs1336265247 Functional Loss SNV ICGC 33..33 33 LAML 1 - 53063 RMVar_ID_53063 Human_SNP_ID_828740007 A-to-I Human chr17 + 39478374 39478374 39478374 CCACCATATCCGGATAATTTTTTTGTATTTTTAGTAGAGACAGGGTTTCATCATGTCATCCAGGC CCACCATATCCGGATAATTTTTTTGTATTTTTCGTAGAGACAGGGTTTCATCATGTCATCCAGGC A C CDK12 Ensembl:ENSG00000167258 Protein coding intron GSE38233 cultured B-cells chr17:39478373..39478374 24183664 RNA-Seq:(High) rs1006188387 Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_12994289 53064 RMVar_ID_53064 Human_SNP_ID_828748860 A-to-I Human chr17 - 68425342 68425342 68425342 AAAATTAGCCGGGTGTGGTGTCACGTGCCTGTAGTCCCAGCTATTCGGGACGCTGAGATGGGAGG AAAATTAGCCGGGTGTGGTGTCACGTGCCTGTGGTCCCAGCTATTCGGGACGCTGAGATGGGAGG T C WIPI1 Ensembl:ENSG00000070540 Protein coding intron GSE100210 HepG2 cell line chr17:68425341..68425342 29129909 RNA-Seq:(High) rs1568619369 Functional Loss SNV ICGC 33..33 33 BRCA 1 - RMVar_hsa_circ_120345,RMVar_hsa_circ_186794,RMVar_hsa_circ_110301,RMVar_hsa_circ_186793 53065 RMVar_ID_53065 Human_SNP_ID_828757138 A-to-I Human chr17 + 75797313 75797313 75797313 GCTGGAGTGCGGTGGCGCAATCTCGGCTCACTACAACCTCTGCCTCCCAGGCTCAAGCAGTTGTC GCTGGAGTGCGGTGGCGCAATCTCGGCTCACTGCAACCTCTGCCTCCCAGGCTCAAGCAGTTGTC A G UNK Ensembl:ENSG00000132478 Protein coding intron GSE47997 K562 cells&HepG2 cells chr17:75797312..75797313 23474544 RNA-Seq:(High) rs1182126892 Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 1 prostate 53066 RMVar_ID_53066 Human_SNP_ID_828765991 A-to-I Human chr17 - 75943098 75943098 75943098 CCTCAGCCTCCTGAGTAGCTGGGATTACAGGCACCTGCCATCACGCTCGGCTAATTTTTGTATTT CCTCAGCCTCCTGAGTAGCTGGGATTACAGGCCCCTGCCATCACGCTCGGCTAATTTTTGTATTT T G ACOX1 Ensembl:ENSG00000161533 Protein coding 3'UTR GSE99789 esophageal squamous carcinoma cells,EC109 chr17:75943097..75943098 29796672 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 2 liver Human_Splice_Rec_1870094 53067 RMVar_ID_53067 Human_SNP_ID_828792201 A-to-I Human chr17 + 60530457 60530457 60530457 GCTGGAGTGCAGTGGCAGGATATCAGCTCACTACAGCCTCAGCCTCACAGGCTCAAGCAGTCTTC GCTGGAGTGCAGTGGCAGGATATCAGCTCACTGCAGCCTCAGCCTCACAGGCTCAAGCAGTCTTC A G AC011921.1 Ensembl:ENSG00000259349 lincRNA intron GSE100210 HepG2 cell line chr17:60530456..60530457 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - 53068 RMVar_ID_53068 Human_SNP_ID_828799884 A-to-I Human chr17 + 38759816 38759816 38759816 TGATCCACCCACCTCGGCCTCCCAAAGTGCTGAGATTACAGGTGTGAGCCACCGCGCCTGGCCCA TGATCCACCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGCGCCTGGCCCA A G PSMB3 Ensembl:ENSG00000277791 Protein coding intron GSE47997 K562 cells&HepG2 cells chr17:38759815..38759816 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_88325,RMVar_hsa_circ_183818,RMVar_hsa_circ_91349,RMVar_hsa_circ_183819,RMVar_hsa_circ_183820,RMVar_hsa_circ_95821 53069 RMVar_ID_53069 Human_SNP_ID_828800072 A-to-I Human chr17 + 5426903 5426903 5426903 TGACTTCGTGATCCACCCACTTCAGCCTTCCAAAGTGCTGGGATTACAGGTGTGAGCCACCACGC TGACTTCGTGATCCACCCACTTCAGCCTTCCACAGTGCTGGGATTACAGGTGTGAGCCACCACGC A C RPAIN Ensembl:ENSG00000129197 Protein coding intron GSE100210 HepG2 cell line chr17:5426903..5426904 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - RMVar_hsa_circ_6190 53070 RMVar_ID_53070 Human_SNP_ID_828800503 A-to-I Human chr17 - 42208870 42208870 42208870 AAAATTAGCCGGGTGTAGTTGTGGGCACCTGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA AAAATTAGCCGGGTGTAGTTGTGGGCACCTGTGGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGA T C STAT5B Ensembl:ENSG00000173757 Protein coding intron GSE38233 cultured B-cells chr17:42208869..42208870 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_131844 RMVar_hsa_circ_53270,RMVar_hsa_circ_184316,RMVar_hsa_circ_265442,RMVar_hsa_circ_71461,RMVar_hsa_circ_303239,RMVar_hsa_circ_317116,RMVar_hsa_circ_56325,RMVar_hsa_circ_184317 53071 RMVar_ID_53071 Human_SNP_ID_828803865 A-to-I Human chr17 + 67978571 67978571 67978571 CGCCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGATGTGAGCCACCGTGCCCGGCCAGAAATT CGCCTGCCTCAGCCTCCCAAAGTGCTGGGATTGCAGATGTGAGCCACCGTGCCCGGCCAGAAATT A G BPTF Ensembl:ENSG00000171634 Protein coding intron GSE38233 cultured B-cells chr17:67978570..67978571 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 53072 RMVar_ID_53072 Human_SNP_ID_828830182 A-to-I Human chr17 - 1439007 1439007 1439007 CAACGTGGTGAAACCCCATCTCTACAAAAAATACAAAAATTAGCCGGGCGTGGTGGCGTGTGCCT CAACGTGGTGAAACCCCATCTCTACAAAAAATGCAAAAATTAGCCGGGCGTGGTGGCGTGTGCCT T C CRK Ensembl:ENSG00000167193 Protein coding intron GSE38233 cultured B-cells chr17:1439006..1439007 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 53073 RMVar_ID_53073 Human_SNP_ID_828830451 A-to-I Human chr17 - 51223822 51223818 51223822 GAAATTGTTGTTGTTGTTGTTGAGACAGTCTCACTCTGATGCCCAAGCTGGAGTGCAGTGGTGCA GAAATTGTTGTTGTTGTTGTTGAGACAGTCTC____TGATGCCCAAGCTGGAGTGCAGTGGTGCA AGAGT A MBTD1 Ensembl:ENSG00000011258 Protein coding intron GSE100210 HepG2 cell line chr17:51223821..51223822 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 33..36 33 MALY 1 - Human_RBP_ID_21927568 RMVar_hsa_circ_337618,RMVar_hsa_circ_6785,RMVar_hsa_circ_297460,RMVar_hsa_circ_185458,RMVar_hsa_circ_185461,RMVar_hsa_circ_105181,RMVar_hsa_circ_297091,RMVar_hsa_circ_10706,RMVar_hsa_circ_185463,RMVar_hsa_circ_326489,RMVar_hsa_circ_185471,RMVar_hsa_circ_276868,RMVar_hsa_circ_326675,RMVar_hsa_circ_77547,RMVar_hsa_circ_185469,RMVar_hsa_circ_185470,RMVar_hsa_circ_292708,RMVar_hsa_circ_185472 53074 RMVar_ID_53074 Human_SNP_ID_828840050 A-to-I Human chr17 - 46171471 46171471 46171471 GCCTTGATGTAGAACACACAACTTTGTATAGCAATAATAGCACTGCAAACAAATCCTCTGTCAAT GCCTTGATGTAGAACACACAACTTTGTATAGCGATAATAGCACTGCAAACAAATCCTCTGTCAAT T C KANSL1 Ensembl:ENSG00000120071 Protein coding CDS GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank chr17:46171470..46171471 30559470 RNA-Seq:(High) rs35643216 Functional Loss SNV COSMIC 33..33 33 pancreas ductal_carcinoma 6 pancreas Human_RBP_ID_300950,Human_RBP_ID_1535370,Human_RBP_ID_1860326,Human_RBP_ID_13039087,Human_RBP_ID_17262935,Human_RBP_ID_17491713,Human_RBP_ID_18700031,Human_RBP_ID_21890744,Human_RBP_ID_22805006,Human_RBP_ID_26963500,Human_RBP_ID_27453463 Human_miRNA_ID_2049912,Human_miRNA_ID_2049913,Human_miRNA_ID_2049914,Human_miRNA_ID_2049915,Human_miRNA_ID_2049916,Human_miRNA_ID_2049917 Clinvar_Rec_117 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_308289,RMVar_hsa_circ_325152,RMVar_hsa_circ_365244,RMVar_hsa_circ_184850 53075 RMVar_ID_53075 Human_SNP_ID_828849077 A-to-I Human chr17 + 60513240 60513240 60513240 GGCGAGCATTCGACTTCCACCTGAAGTAAATCAGATATTGTATATAAGAAATTTGCCATACACAA GGCGAGCATTCGACTTCCACCTGAAGTAAATCGGATATTGTATATAAGAAATTTGCCATACACAA A G AC011921.3 Ensembl:ENSG00000270553 Pseudogene exon GSE100210 HepG2 cell line chr17:60513239..60513240 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue 53076 RMVar_ID_53076 Human_SNP_ID_828851484 A-to-I Human chr17 + 40257557 40257557 40257557 ACCTGAGGCCAGGCGCGATGGCTCACGCCTGTAATCCCAACACTTTGGGAGGCTGAGGTGGGTGG ACCTGAGGCCAGGCGCGATGGCTCACGCCTGTTATCCCAACACTTTGGGAGGCTGAGGTGGGTGG A T WIPF2 Ensembl:ENSG00000171475 Protein coding intron GSE38233 cultured B-cells chr17:40257556..40257557;chr17:40257557..40257558 24183664 RNA-Seq:(High) rs1238074095 Functional Loss SNV ICGC 33..33 33 LUSC 1 - RMVar_hsa_circ_184037,RMVar_hsa_circ_327377,RMVar_hsa_circ_377483,RMVar_hsa_circ_296932 53077 RMVar_ID_53077 Human_SNP_ID_828858750 A-to-I Human chr17 - 82256346 82256346 82256346 ACCACACCCACCTAATTTCCAGAATTTTTTGTAGAGACAAGGGTCTCCCTTTGTTATCCAGGCTG ACCACACCCACCTAATTTCCAGAATTTTTTGTGGAGACAAGGGTCTCCCTTTGTTATCCAGGCTG T C CSNK1D Ensembl:ENSG00000141551 Protein coding intron GSE100210 HepG2 cell line chr17:82256345..82256346 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_2526876,Human_RBP_ID_13204077,Human_RBP_ID_22958654 RMVar_hsa_circ_293756,RMVar_hsa_circ_187926,RMVar_hsa_circ_343316,RMVar_hsa_circ_339301,RMVar_hsa_circ_368813 53078 RMVar_ID_53078 Human_SNP_ID_828863064 A-to-I Human chr17 - 5035073 5035073 5035073 AATCTCCTGACCTCAGGCGATCTGCCTTCCTCAGCTTCCCAAAGTGCTGGGATTACAGGTGTGAG AATCTCCTGACCTCAGGCGATCTGCCTTCCTCGGCTTCCCAAAGTGCTGGGATTACAGGTGTGAG T C SLC52A1 Ensembl:ENSG00000132517 Protein coding intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line chr17:5035072..5035073 32596459 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 53079 RMVar_ID_53079 Human_SNP_ID_828872256 A-to-I Human chr17 + 74205944 74205944 74205944 CAGGAGGCTGAGGCAGGAGAATCAGTTGAACCAAGGAGACGGAGGTTGCAGTGAGCTGAGATTGT CAGGAGGCTGAGGCAGGAGAATCAGTTGAACCGAGGAGACGGAGGTTGCAGTGAGCTGAGATTGT A G RPL38 Ensembl:ENSG00000172809 Protein coding intron GSE38233 cultured B-cells chr17:74205944..74205945 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_13155191,Human_RBP_ID_25323377 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 53080 RMVar_ID_53080 Human_SNP_ID_828877021 A-to-I Human chr17 + 77202781 77202781 77202781 GTCTCTAGTAAAATACAAAAAATTAGCCGGGCATGGCAGCGTGCGCCTGTAGTTCCAGCTACTTG GTCTCTAGTAAAATACAAAAAATTAGCCGGGCGTGGCAGCGTGCGCCTGTAGTTCCAGCTACTTG A G SEC14L1 Ensembl:ENSG00000129657 Protein coding intron GSE38233 cultured B-cells chr17:77202780..77202781 24183664 RNA-Seq:(High) rs8080207 Functional Loss SNV COSMIC 33..33 33 central_nervous_system oligodendroglioma_Grade_III,frontal_lobe oligodendroglioma_Grade_III 7 brain GWAS_ID_4951,GWAS_ID_4952,GWAS_ID_4953,GWAS_ID_4954,GWAS_ID_4955,GWAS_ID_4956 RMVar_hsa_circ_98284,RMVar_hsa_circ_118861,RMVar_hsa_circ_187286,RMVar_hsa_circ_97983,RMVar_hsa_circ_187287,RMVar_hsa_circ_187285 53081 RMVar_ID_53081 Human_SNP_ID_828894387 A-to-I Human chr17 - 35151197 35151197 35151197 CGCTGAATTTAAGCATATTTGTCAGCGGAGGAAAAGAAACTAACCAGGATTCCCTCAGTAATGGC CGCTGAATTTAAGCATATTTGTCAGCGGAGGAGAAGAAACTAACCAGGATTCCCTCAGTAATGGC T C RF02543-021 RNACentral:URS000096B15F rRNA intron GSE38233 cultured B-cells chr17:35151196..35151197 24183664 RNA-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 53082 RMVar_ID_53082 Human_SNP_ID_828913728 A-to-I Human chr17 - 35078378 35078378 35078378 GGATTGCTTGAGTCCAGGAGTTTGAGGTTATAATGAACTATGGTTGCACAACTGTACTCTAGTGT GGATTGCTTGAGTCCAGGAGTTTGAGGTTATATTGAACTATGGTTGCACAACTGTACTCTAGTGT T A RFFL,AC004223.3 Ensembl:ENSG00000092871,Ensembl:ENSG00000267618 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells chr17:35078377..35078378 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 5 prostate Human_RBP_ID_1181287 53083 RMVar_ID_53083 Human_SNP_ID_828956389 A-to-I Human chr17 + 2127692 2127692 2127692 ACTCTGCTCTTTTCTAGGTTGAAGTCTAATTTAGTATCTGTTCGGACTTTAATCACTTCATCCAT ACTCTGCTCTTTTCTAGGTTGAAGTCTAATTTGGTATCTGTTCGGACTTTAATCACTTCATCCAT A G RF00017-156 RNACentral:URS000091874B SRP RNA intron GSE100210 HepG2 cell line chr17:2127691..2127692 29129909 RNA-Seq:(High) rs1274834098 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 8 haematopoietic and lymphoid tissue 53084 RMVar_ID_53084 Human_SNP_ID_828970384 A-to-I Human chr17 + 43136022 43136022 43136022 TAAAAGGGCTTAATACAGGCTTCGCCGGGCGCAGGGCTCCCGCCTGTAATTCCAGTACTTTGGGA TAAAAGGGCTTAATACAGGCTTCGCCGGGCGCGGGGCTCCCGCCTGTAATTCCAGTACTTTGGGA A G NBR2 Ensembl:ENSG00000198496 lincRNA intron GSE100210 HepG2 cell line chr17:43136021..43136022 29129909 RNA-Seq:(High) rs988536331 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_6596995,Human_RBP_ID_13015759,Human_RBP_ID_18698639,Human_RBP_ID_22357281 53085 RMVar_ID_53085 Human_SNP_ID_828972452 A-to-I Human chr17 - 81561238 81561238 81561238 CAAAAGGAAATGCAGGTCGGGCATGGTAGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAG CAAAAGGAAATGCAGGTCGGGCATGGTAGCTCGCGCCTGTAATCCCAGCACTTTGGGAGGCCGAG T C NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr17:81561237..81561238 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 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 53086 RMVar_ID_53086 Human_SNP_ID_828977306 A-to-I Human chr17 + 82483239 82483239 82483239 TACTCAGGAGGCTGCGGCAAGAGAATCACTTGAACCCGGGAGGCAGAGGTTACAGCGAGACAAGA TACTCAGGAGGCTGCGGCAAGAGAATCACTTGGACCCGGGAGGCAGAGGTTACAGCGAGACAAGA A G NARF,NARF-IT1 Ensembl:ENSG00000141562,Ensembl:ENSG00000266236 Protein coding,lincRNA intron,intron GSE38233 cultured B-cells chr17:82483238..82483239 24183664 RNA-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_3953399,Human_RBP_ID_26334008 Human_Splice_Rec_1885932,Human_Splice_Rec_1885933,Human_Splice_Rec_1885945,Human_Splice_Rec_1885964,Human_Splice_Rec_1885965 RMVar_hsa_circ_279444,RMVar_hsa_circ_101494,RMVar_hsa_circ_187958 53087 RMVar_ID_53087 Human_SNP_ID_828992365 A-to-I Human chr17 - 40024449 40024449 40024449 GCTCACTGCAATCTCCGCCTCCTGGGTTCAAGAGATTCTCCTGCCTCAGCCTCCCGAGTAGCCGG GCTCACTGCAATCTCCGCCTCCTGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCCGG T G MED24 Ensembl:ENSG00000008838 Protein coding intron GSE47997 K562 cells&HepG2 cells chr17:40024448..40024449 23474544 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 meninges anaplastic 6 brain 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 53088 RMVar_ID_53088 Human_SNP_ID_828993453 A-to-I Human chr17 + 55770935 55770931 55770936 TTTTTTTATATATAGAGATGGGGTTTCACCATATTTCCCAGGCTGGTCTTGAACTCCTGGACTTG TTTTTTTATATATAGAGATGGGGTTTCAC_____TTCCCAGGCTGGTCTTGAACTCCTGGACTTG CCATAT C PCTP Ensembl:ENSG00000141179 Protein coding intron GSE100210 HepG2 cell line chr17:55770934..55770935 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 30..34 33 PAAD 1 - RMVar_hsa_circ_33245,RMVar_hsa_circ_185534,RMVar_hsa_circ_284824,RMVar_hsa_circ_185535 53089 RMVar_ID_53089 Human_SNP_ID_829024918 A-to-I Human chr17 + 82594790 82594789 82594790 AGGAACAGCTGGGCGCCGTGGCTCACGCCTGCAATCCCAGCACTTTGGAAGACCAGGGTGGGCAG AGGAACAGCTGGGCGCCGTGGCTCACGCCTGC_ATCCCAGCACTTTGGAAGACCAGGGTGGGCAG CA C FOXK2 Ensembl:ENSG00000141568 Protein coding intron GSE100210 HepG2 cell line chr17:82594790..82594791 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 33..33 33 PRAD 1 - 53090 RMVar_ID_53090 Human_SNP_ID_829026567 A-to-I Human chr17 - 50761210 50761210 50761210 GAAACCCAGTCTCTACTAAAAAAAATACAAAAATTAGCTAGGTGTGGTGGCGCACACCTGTAGTA GAAACCCAGTCTCTACTAAAAAAAATACAAAATTTAGCTAGGTGTGGTGGCGCACACCTGTAGTA T A ANKRD40CL Ensembl:ENSG00000167117 Protein coding exon GSE47997 K562 cells&HepG2 cells chr17:50761209..50761210 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 2 breast 53091 RMVar_ID_53091 Human_SNP_ID_829034138 A-to-I Human chr17 + 75800314 75800314 75800314 GCTGGTCTCCAATTCCTGAGCTCAAGCGATCCACCCGCCTTGGCCTCTCAGAGTGCTGGGATTAC GCTGGTCTCCAATTCCTGAGCTCAAGCGATCCCCCCGCCTTGGCCTCTCAGAGTGCTGGGATTAC A C UNK Ensembl:ENSG00000132478 Protein coding intron GSE100210 HepG2 cell line chr17:75800313..75800314 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_13165006,Human_RBP_ID_22717504 53092 RMVar_ID_53092 Human_SNP_ID_829053199 A-to-I Human chr17 - 81251243 81251243 81251243 ACACCTGCGGCATCGTCACATGGCTTGTGATTACCGTTTTATCTCCCTTGCTCCCCTTTAAAACA ACACCTGCGGCATCGTCACATGGCTTGTGATTTCCGTTTTATCTCCCTTGCTCCCCTTTAAAACA T A SLC38A10 Ensembl:ENSG00000157637 Protein coding intron GSE112787 293 Flip-In T-REx cells,empty vector chr17:81251242..81251243 29967493 RNA-Seq:(High) - 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_3539452,Human_RBP_ID_13194596,Human_RBP_ID_17080351,Human_RBP_ID_18487768,Human_RBP_ID_20280959 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_187591 53093 RMVar_ID_53093 Human_SNP_ID_829055210 A-to-I Human chr17 - 28715058 28715058 28715058 CGCCCTCCAGGTGGCCCAGGAGATGAAGGCTGAGTACTGGGCAGTCTCATCTCTCACTGGTGAGT CGCCCTCCAGGTGGCCCAGGAGATGAAGGCTGGGTACTGGGCAGTCTCATCTCTCACTGGTGAGT T C RAB34 Ensembl:ENSG00000109113 Protein coding intron GSE100210 HepG2 cell line chr17:28715057..28715058 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 10 liver Human_RBP_ID_485923,Human_RBP_ID_17888052,Human_RBP_ID_23717984 Human_Splice_Rec_1796714,Human_Splice_Rec_1796728,Human_Splice_Rec_1796729,Human_Splice_Rec_1796746,Human_Splice_Rec_1796747,Human_Splice_Rec_1796766,Human_Splice_Rec_1796782,Human_Splice_Rec_1796783,Human_Splice_Rec_1796802,Human_Splice_Rec_1796803,Human_Splice_Rec_1796820,Human_Splice_Rec_1796821,Human_Splice_Rec_1796827,Human_Splice_Rec_1796844,Human_Splice_Rec_1796845,Human_Splice_Rec_1796868,Human_Splice_Rec_1796869,Human_Splice_Rec_1796884,Human_Splice_Rec_1796885,Human_Splice_Rec_1796898,Human_Splice_Rec_1796899,Human_Splice_Rec_1796914,Human_Splice_Rec_1796915,Human_Splice_Rec_1796932,Human_Splice_Rec_1796933,Human_Splice_Rec_1796950,Human_Splice_Rec_1796951,Human_Splice_Rec_1796964 Human_miRNA_ID_2678976,Human_miRNA_ID_2678977,Human_miRNA_ID_2678978,Human_miRNA_ID_3081019,Human_miRNA_ID_3081020,Human_miRNA_ID_3081021,Human_miRNA_ID_3086609,Human_miRNA_ID_3086610,Human_miRNA_ID_3086611 RMVar_hsa_circ_115193,RMVar_hsa_circ_116861,RMVar_hsa_circ_125718,RMVar_hsa_circ_128144,RMVar_hsa_circ_119538,RMVar_hsa_circ_115553,RMVar_hsa_circ_112836,RMVar_hsa_circ_182993,RMVar_hsa_circ_76140,RMVar_hsa_circ_98415,RMVar_hsa_circ_80876,RMVar_hsa_circ_182997,RMVar_hsa_circ_182999,RMVar_hsa_circ_183001,RMVar_hsa_circ_183002,RMVar_hsa_circ_183000,RMVar_hsa_circ_182998,RMVar_hsa_circ_182995,RMVar_hsa_circ_182996,RMVar_hsa_circ_182994,RMVar_hsa_circ_24307 53094 RMVar_ID_53094 Human_SNP_ID_829063132 A-to-I Human chr17 - 2300054 2300054 2300054 GGGGAGGGGGTGAGGGAAACCCACGACGACCCAGCCCGCGGGAGGCCGGGCTCCGCAAAGCGCTA GGGGAGGGGGTGAGGGAAACCCACGACGACCCGGCCCGCGGGAGGCCGGGCTCCGCAAAGCGCTA T C SMG6 Ensembl:ENSG00000070366 Protein coding CDS GSE38233 cultured B-cells chr17:2300053..2300054 24183664 RNA-Seq:(High) rs216194 Functional Loss SNV ICGC 33..33 33 COCA 5 - Human_RBP_ID_235684,Human_RBP_ID_764414,Human_RBP_ID_819412,Human_RBP_ID_903101,Human_RBP_ID_5525197,Human_RBP_ID_9422164,Human_RBP_ID_25257790 GWAS_ID_5508 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 53095 RMVar_ID_53095 Human_SNP_ID_829075917 A-to-I Human chr17 - 82145153 82145153 82145153 AGCCAAGTGTTGGGGCACGTGCCTGTAATCCCAGCTACTCGGGCGGCTGAGGCAGGAGAATCTCG AGCCAAGTGTTGGGGCACGTGCCTGTAATCCCGGCTACTCGGGCGGCTGAGGCAGGAGAATCTCG T C CCDC57 Ensembl:ENSG00000176155 Protein coding intron GSE100210 HepG2 cell line chr17:82145152..82145153 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 4 oesophagus RMVar_hsa_circ_31577,RMVar_hsa_circ_187899,RMVar_hsa_circ_85460,RMVar_hsa_circ_36569,RMVar_hsa_circ_25796,RMVar_hsa_circ_269498 53096 RMVar_ID_53096 Human_SNP_ID_829076895 A-to-I Human chr17 - 37154185 37154185 37154185 GTCCCATGTCAGCCTCCCAAGTAGCTGGGACTATAGACAGGTGCCATCATGCCCAGCTAATTATT GTCCCATGTCAGCCTCCCAAGTAGCTGGGACTGTAGACAGGTGCCATCATGCCCAGCTAATTATT T C ACACA Ensembl:ENSG00000278540 Protein coding intron GSE100210 HepG2 cell line chr17:37154184..37154185 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_26159,RMVar_hsa_circ_32188,RMVar_hsa_circ_74902,RMVar_hsa_circ_306981,RMVar_hsa_circ_326218,RMVar_hsa_circ_314445,RMVar_hsa_circ_303283,RMVar_hsa_circ_57998,RMVar_hsa_circ_14902,RMVar_hsa_circ_23530 53097 RMVar_ID_53097 Human_SNP_ID_829081632 A-to-I Human chr17 - 43389003 43389003 43389003 GAGGTGCGATGAAATACACAGGAGGGCTGCTAATCACATATGGGGTGGGTGCCGAGGGCCCTTAA GAGGTGCGATGAAATACACAGGAGGGCTGCTAGTCACATATGGGGTGGGTGCCGAGGGCCCTTAA T C LINC00910 Ensembl:ENSG00000188825 lincRNA intron GSE100210 HepG2 cell line chr17:43389002..43389003 29129909 RNA-Seq:(High) rs77256558 Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_819649,Human_RBP_ID_2507693,Human_RBP_ID_5097959,Human_RBP_ID_5649201,Human_RBP_ID_6597475,Human_RBP_ID_13017068 53098 RMVar_ID_53098 Human_SNP_ID_829135560 A-to-I Human chr17 - 48934560 48934559 48934560 TTGCTCTGTTGTCTAGGCTGGAGCGCAGTGGTACAATCTCGGCTCACTGCAACCTCCGCCTCCTG TTGCTCTGTTGTCTAGGCTGGAGCGCAGTGGT_CAATCTCGGCTCACTGCAACCTCCGCCTCCTG GT G SNF8 Ensembl:ENSG00000159210 Protein coding intron GSE100210 HepG2 cell line chr17:48934559..48934560 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 33..33 33 PAAD 1 - Human_RBP_ID_13220310 Human_Splice_Rec_1835188,Human_Splice_Rec_1835189 RMVar_hsa_circ_122023,RMVar_hsa_circ_185120 53099 RMVar_ID_53099 Human_SNP_ID_829142520 A-to-I Human chr17 + 80341725 80341705 80341726 ACGACACTGCACTCCAGCCTAGGCAACGGGGCAAGGCCTTGGTCTTTTAAAAAAAGAGAAAGAAA ACGACACTGCACT_____________________GGCCTTGGTCTTTTAAAAAAAGAGAAAGAAA TCCAGCCTAGGCAACGGGGCAA T AC124319.3,RNF213 Ensembl:ENSG00000280248,Ensembl:ENSG00000173821 Other,Protein coding exon,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr17:80341724..80341725 24183664,29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 14..34 33 ESCA 1 - 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_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 53100 RMVar_ID_53100 Human_SNP_ID_829182360 A-to-I Human chr17 + 59201709 59201709 59201709 ATAAAAACACCCAGCTGGGTGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGC ATAAAAACACCCAGCTGGGTGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGC A G AC099850.3,PRR11 Ensembl:ENSG00000265303,Ensembl:ENSG00000068489 Protein coding,Protein coding intron,3'UTR GSE47997;GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line chr17:59201708..59201709 23474544,24183664,29129909,31158229,31158229,31158229,32596459 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 testis seminoma 3 testis Human_Splice_Rec_1847035,Human_Splice_Rec_1847077,Human_Splice_Rec_1847097 Human_miRNA_ID_1738467,Human_miRNA_ID_1943418,Human_miRNA_ID_1946455,Human_miRNA_ID_2117609,Human_miRNA_ID_2201191,Human_miRNA_ID_2204254,Human_miRNA_ID_2316800,Human_miRNA_ID_2319953,Human_miRNA_ID_2323112,Human_miRNA_ID_2326286,Human_miRNA_ID_2520663,Human_miRNA_ID_2523829,Human_miRNA_ID_2775646,Human_miRNA_ID_2816704,Human_miRNA_ID_2823014,Human_miRNA_ID_2829148,Human_miRNA_ID_2832303,Human_miRNA_ID_2836426,Human_miRNA_ID_2841778,Human_miRNA_ID_2846827,Human_miRNA_ID_2849849,Human_miRNA_ID_2863970,Human_miRNA_ID_2891094,Human_miRNA_ID_3113703 RMVar_hsa_circ_97892,RMVar_hsa_circ_185763 53101 RMVar_ID_53101 Human_SNP_ID_829192119 A-to-I Human chr17 - 10674357 10674357 10674357 CAGTGGTGCGATCTTGGCTCACTGCAACCTCCACCTCCCTGGTTCAAGTGATTCTGCTGCCTCAG CAGTGGTGCGATCTTGGCTCACTGCAACCTCCCCCTCCCTGGTTCAAGTGATTCTGCTGCCTCAG T G SCO1 Ensembl:ENSG00000133028 Protein coding 3'UTR GSE100210 HepG2 cell line chr17:10674356..10674357 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 53102 RMVar_ID_53102 Human_SNP_ID_829205634 A-to-I Human chr17 - 18271812 18271812 18271812 GTGATCTACCAGCCTCGGCCTCCCAAAGTGCTAGGATTAACAGGCAGGAGCCATCACACCTGGTC GTGATCTACCAGCCTCGGCCTCCCAAAGTGCTGGGATTAACAGGCAGGAGCCATCACACCTGGTC T C TOP3A Ensembl:ENSG00000177302 Protein coding intron GSE38233;GSE100210;GSE112787 cultured B-cells;HepG2 cell line;293 Flip-In T-REx cells,empty vector chr17:18271811..18271812 24183664,29129909,29967493 RNA-Seq:(High) rs1409333650 Functional Loss SNV ICGC 33..33 33 LICA 1 - 53103 RMVar_ID_53103 Human_SNP_ID_829242200 A-to-I Human chr17 + 28672477 28672477 28672477 CTCTTGTTGCCCAGGCTGGAGTGCAGTGGTGCAATCTCAGCTCACTGCAACCTCCACCTCCCGGG CTCTTGTTGCCCAGGCTGGAGTGCAGTGGTGCGATCTCAGCTCACTGCAACCTCCACCTCCCGGG A G SUPT6H Ensembl:ENSG00000109111 Protein coding intron GSE38233 cultured B-cells chr17:28672476..28672477;chr17:28672477..28672478 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 53104 RMVar_ID_53104 Human_SNP_ID_829261535 A-to-I Human chr17 - 51824989 51824989 51824989 ATAATAAAGAAAATGCAACAAAATGATCCGAAAGTTAAACAGCAGGCAGTATAGACAGTGGTACT ATAATAAAGAAAATGCAACAAAATGATCCGAACGTTAAACAGCAGGCAGTATAGACAGTGGTACT T G CA10 Ensembl:ENSG00000154975 Protein coding intron GSE107867 ASD brains,cerebellum chr17:51824988..51824989 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 5 oesophagus 53105 RMVar_ID_53105 Human_SNP_ID_829282851 A-to-I Human chr17 + 2127710 2127710 2127710 TTGAAGTCTAATTTAGTATCTGTTCGGACTTTAATCACTTCATCCATTACTTGTTTTAACTGATG TTGAAGTCTAATTTAGTATCTGTTCGGACTTTGATCACTTCATCCATTACTTGTTTTAACTGATG A G RF00017-156 RNACentral:URS000091874B SRP RNA intron GSE100210 HepG2 cell line chr17:2127709..2127710 29129909 RNA-Seq:(High) rs533694208 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 8 haematopoietic and lymphoid tissue 53106 RMVar_ID_53106 Human_SNP_ID_829285761 A-to-I Human chr17 - 43807248 43807248 43807248 TAAGGGGGAGGCTGGCATGGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCTGAGGCAGGC TAAGGGGGAGGCTGGCATGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGC T C MPP3 Ensembl:ENSG00000161647 Protein coding intron GSE100210 HepG2 cell line chr17:43807247..43807248 29129909 RNA-Seq:(High) rs1339788380 Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_99276,RMVar_hsa_circ_184611 53107 RMVar_ID_53107 Human_SNP_ID_829296458 A-to-I Human chr17 + 60513316 60513316 60513316 TCAATGTATATTTGGGAAATATGGACCTATTCATCAAATCAGAGTGGAAAACACACCTGAAACTA TCAATGTATATTTGGGAAATATGGACCTATTCGTCAAATCAGAGTGGAAAACACACCTGAAACTA A G AC011921.3 Ensembl:ENSG00000270553 Pseudogene exon GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr17:60513315..60513316 24183664,29129909 RNA-Seq:(High) rs879039940 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue Human_RBP_ID_5579877,Human_RBP_ID_9078115 53108 RMVar_ID_53108 Human_SNP_ID_829296534 A-to-I Human chr17 - 81884088 81884088 81884088 CGTGTGTGGTGGCATGATTTCACCTCACTGCAACCTCCGCCTCCCGGGTTGAATCGATTCTCCTG CGTGTGTGGTGGCATGATTTCACCTCACTGCACCCTCCGCCTCCCGGGTTGAATCGATTCTCCTG T G - - Other Unknown GSE100210 HepG2 cell line chr17:81884087..81884088 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_13200596,Human_RBP_ID_17693356,Human_RBP_ID_17903054 53109 RMVar_ID_53109 Human_SNP_ID_829320322 A-to-I Human chr17 + 32227947 32227947 32227947 CCATTGTGGATTTCATAGTCCCCCAGAGACACATGGTCCTTAAAAATTGTGTACCACTTCTTCAG CCATTGTGGATTTCATAGTCCCCCAGAGACACGTGGTCCTTAAAAATTGTGTACCACTTCTTCAG A G RHOT1 Ensembl:ENSG00000126858 Protein coding intron GSE100210 HepG2 cell line chr17:32227946..32227947 29129909 RNA-Seq:(High) rs879208186 Functional Loss SNV ICGC 33..33 33 LAML 2 - 53110 RMVar_ID_53110 Human_SNP_ID_829347359 A-to-I Human chr17 - 10673197 10673197 10673197 GAGATCGAGATCATCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAATTACAAAAATCAGCT GAGATCGAGATCATCCTGGCCAACATGGTGAACCCCCATCTCTACTAAAATTACAAAAATCAGCT T G SCO1 Ensembl:ENSG00000133028 Protein coding 3'UTR GSE100210 HepG2 cell line chr17:10673196..10673197 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 53111 RMVar_ID_53111 Human_SNP_ID_829404748 A-to-I Human chr17 + 78192279 78192279 78192279 GTGATTCGCCCTCCTCGGCCTCCCAAAGTGCTAGGATTACAGGTGTGAGCCACCATGGCTGGACT GTGATTCGCCCTCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCATGGCTGGACT A G AFMID Ensembl:ENSG00000183077 Protein coding intron GSE100210 HepG2 cell line chr17:78192278..78192279 29129909 RNA-Seq:(High) rs1162741005 Functional Loss SNV ICGC 33..33 33 PBCA 1 - 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 53112 RMVar_ID_53112 Human_SNP_ID_829411349 A-to-I Human chr17 - 65655302 65655302 65655302 ATTTTCATCGAGAAATCCAGCTGTAGTGTCTGAGGCTGCGGTCGCTCAGCCTGCACCCAACAAAG ATTTTCATCGAGAAATCCAGCTGTAGTGTCTGGGGCTGCGGTCGCTCAGCCTGCACCCAACAAAG T C CEP112 Ensembl:ENSG00000154240 Protein coding intron GSE100210 HepG2 cell line chr17:65655301..65655302 29129909 RNA-Seq:(High) rs878902265 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 5 haematopoietic and lymphoid tissue RMVar_hsa_circ_186547,RMVar_hsa_circ_376420,RMVar_hsa_circ_186548 53113 RMVar_ID_53113 Human_SNP_ID_829420684 A-to-I Human chr17 - 50964331 50964331 50964331 TACCCGCCTTGGCCTCCCGAAGTGCTTGAATTACAGGCGTGAGCCCCCGCGCCGGTCCGAAGCAA TACCCGCCTTGGCCTCCCGAAGTGCTTGAATTGCAGGCGTGAGCCCCCGCGCCGGTCCGAAGCAA T C SPAG9 Ensembl:ENSG00000008294 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr17:50964330..50964331 24183664,29129909 RNA-Seq:(High) rs1055361 Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_26453193 Human_Splice_Rec_1841928 Human_miRNA_ID_2250322 RMVar_hsa_circ_103413,RMVar_hsa_circ_119329,RMVar_hsa_circ_185389,RMVar_hsa_circ_95841,RMVar_hsa_circ_185390,RMVar_hsa_circ_185388 53114 RMVar_ID_53114 Human_SNP_ID_829428388 A-to-I Human chr17 - 31881405 31881405 31881405 AAAATTAGCTGGGCGTGGTGGTATGCGTCTGTAATTCCAGCTACTTGGAAGGCTGAGGCAGGAGA AAAATTAGCTGGGCGTGGTGGTATGCGTCTGTGATTCCAGCTACTTGGAAGGCTGAGGCAGGAGA T C UTP6 Ensembl:ENSG00000108651 Protein coding intron GSE38233 cultured B-cells chr17:31881404..31881405 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_95871,RMVar_hsa_circ_8176,RMVar_hsa_circ_183415,RMVar_hsa_circ_6658,RMVar_hsa_circ_64841,RMVar_hsa_circ_332632,RMVar_hsa_circ_329041,RMVar_hsa_circ_99101,RMVar_hsa_circ_64596,RMVar_hsa_circ_183421,RMVar_hsa_circ_267971,RMVar_hsa_circ_183419,RMVar_hsa_circ_81138,RMVar_hsa_circ_349140,RMVar_hsa_circ_365759,RMVar_hsa_circ_274831,RMVar_hsa_circ_46530,RMVar_hsa_circ_183422 53115 RMVar_ID_53115 Human_SNP_ID_829434181 A-to-I Human chr17 - 17859263 17859263 17859263 CGAGACCAGCCTGACCAACATGGAGAAACCCCATCTCTACTAAAAATACAAAATTAGCTGGGCAT CGAGACCAGCCTGACCAACATGGAGAAACCCCGTCTCTACTAAAAATACAAAATTAGCTGGGCAT T C TOM1L2 Ensembl:ENSG00000175662 Protein coding intron GSE47997 K562 cells&HepG2 cells chr17:17859262..17859263 23474544 RNA-Seq:(High) rs1057367420 Functional Loss SNV ICGC,COSMIC 33..33 33 prostate adenocarcinoma,PRAD 9 prostate RMVar_hsa_circ_108718,RMVar_hsa_circ_182410 53116 RMVar_ID_53116 Human_SNP_ID_829443613 A-to-I Human chr17 + 60513331 60513331 60513331 GAAATATGGACCTATTCATCAAATCAGAGTGGAAAACACACCTGAAACTAGAGGAACAGCTTATG GAAATATGGACCTATTCATCAAATCAGAGTGGGAAACACACCTGAAACTAGAGGAACAGCTTATG A G AC011921.3 Ensembl:ENSG00000270553 Pseudogene exon GSE100210 HepG2 cell line chr17:60513330..60513331;chr17:60513331..60513332 29129909 RNA-Seq:(High) rs879125901 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue Human_RBP_ID_5579877 53117 RMVar_ID_53117 Human_SNP_ID_829462347 A-to-I Human chr17 - 43124925 43124925 43124925 CCTGACCAACGTGGTGAAACTCCGTCTCTACTAAAAATACAAAAATTAGCCGGGCGTGGTGCCGC CCTGACCAACGTGGTGAAACTCCGTCTCTACTGAAAATACAAAAATTAGCCGGGCGTGGTGCCGC T C BRCA1 Ensembl:ENSG00000012048 Protein coding intron GSE100210 HepG2 cell line chr17:43124924..43124925 29129909 RNA-Seq:(High) rs1489102499 Functional Loss SNV ICGC,COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma,CLLE 11 haematopoietic and lymphoid tissue Human_RBP_ID_132929 53118 RMVar_ID_53118 Human_SNP_ID_829468611 A-to-I Human chr17 - 68425500 68425500 68425500 TAAGAAACAAGTGGCCGGGTGCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGC TAAGAAACAAGTGGCCGGGTGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGC T C WIPI1 Ensembl:ENSG00000070540 Protein coding intron GSE100210 HepG2 cell line chr17:68425499..68425500 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - RMVar_hsa_circ_120345,RMVar_hsa_circ_186794,RMVar_hsa_circ_110301,RMVar_hsa_circ_186793 53119 RMVar_ID_53119 Human_SNP_ID_829520982 A-to-I Human chr17 + 5225668 5225668 5225668 CCTGTAATCCCAGCTACTTGAGAGACTGAGGCAAGAGAATTGCTTGAACCTGGGAGTCAGAGGTT CCTGTAATCCCAGCTACTTGAGAGACTGAGGCCAGAGAATTGCTTGAACCTGGGAGTCAGAGGTT A C AC087500.1 Ensembl:ENSG00000261879 lincRNA intron GSE100210 HepG2 cell line chr17:5225668..5225669 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 53120 RMVar_ID_53120 Human_SNP_ID_829566948 A-to-I Human chr17 + 5026500 5026500 5026500 GGCTGGGCACAGAAGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGAGGATCAGT GGCTGGGCACAGAAGCTCACACCTGTAATCCCGGCACTTTGGGAGGCTGAGGCAGGAGGATCAGT A G KIF1C Ensembl:ENSG00000129250 Protein coding 3'UTR GSE38233 cultured B-cells chr17:5026499..5026500 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 RECA 1 - 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 53121 RMVar_ID_53121 Human_SNP_ID_829581357 A-to-I Human chr17 - 19351118 19351118 19351118 AAGTCAGAGTCAGGCCAGGCACCATGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGC AAGTCAGAGTCAGGCCAGGCACCATGGCTCACTCCTGTAATCCCAGCACTTTGGGAGGCCGAGGC T A B9D1 Ensembl:ENSG00000108641 Protein coding intron GSE100210 HepG2 cell line chr17:19351117..19351118 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 11 breast RMVar_hsa_circ_105448,RMVar_hsa_circ_182572 53122 RMVar_ID_53122 Human_SNP_ID_829584161 A-to-I Human chr17 - 39425467 39425467 39425467 CTACAGGCCGTGCCTGGTGGTTCATGCCTGTAATTTCAGCACTGTGGGAGGCTGAGATGGGTGGA CTACAGGCCGTGCCTGGTGGTTCATGCCTGTAGTTTCAGCACTGTGGGAGGCTGAGATGGGTGGA T C MED1 Ensembl:ENSG00000125686 Protein coding intron GSE38233 cultured B-cells chr17:39425466..39425467 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 3 prostate RMVar_hsa_circ_100808,RMVar_hsa_circ_372677,RMVar_hsa_circ_183896,RMVar_hsa_circ_304738,RMVar_hsa_circ_80034,RMVar_hsa_circ_104912,RMVar_hsa_circ_30905,RMVar_hsa_circ_183905,RMVar_hsa_circ_183901,RMVar_hsa_circ_183902,RMVar_hsa_circ_183903,RMVar_hsa_circ_183900,RMVar_hsa_circ_93336,RMVar_hsa_circ_278893,RMVar_hsa_circ_341094,RMVar_hsa_circ_367786,RMVar_hsa_circ_183906,RMVar_hsa_circ_183912,RMVar_hsa_circ_285321,RMVar_hsa_circ_350457,RMVar_hsa_circ_355926,RMVar_hsa_circ_363100,RMVar_hsa_circ_288204,RMVar_hsa_circ_22389,RMVar_hsa_circ_72013,RMVar_hsa_circ_183913,RMVar_hsa_circ_183914,RMVar_hsa_circ_365687,RMVar_hsa_circ_89106,RMVar_hsa_circ_183922,RMVar_hsa_circ_304532,RMVar_hsa_circ_183917,RMVar_hsa_circ_346431,RMVar_hsa_circ_375139,RMVar_hsa_circ_362157,RMVar_hsa_circ_315200,RMVar_hsa_circ_105952,RMVar_hsa_circ_285393,RMVar_hsa_circ_183923,RMVar_hsa_circ_183924,RMVar_hsa_circ_183918,RMVar_hsa_circ_183920,RMVar_hsa_circ_183921,RMVar_hsa_circ_183919 53123 RMVar_ID_53123 Human_SNP_ID_829594477 A-to-I Human chr17 - 28814096 28814096 28814096 TGCTCACTGTACTCTGCCAAGTAGCTGGGACTACCGTGCGAGTTACCACGCCTAGCTACCTCTAA TGCTCACTGTACTCTGCCAAGTAGCTGGGACTGCCGTGCGAGTTACCACGCCTAGCTACCTCTAA T C FAM222B Ensembl:ENSG00000173065 Protein coding intron GSE100210 HepG2 cell line chr17:28814095..28814096 29129909 RNA-Seq:(High) rs550027479 Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_767403 53124 RMVar_ID_53124 Human_SNP_ID_829596863 A-to-I Human chr17 - 76483004 76483004 76483004 GCACTATGCCTGGCTAATTTTTGTATTTTAGTAGAGATGGTGTTTCACTGTGTTGGCCAGGCTAG GCACTATGCCTGGCTAATTTTTGTATTTTAGTGGAGATGGTGTTTCACTGTGTTGGCCAGGCTAG T C RHBDF2 Ensembl:ENSG00000129667 Protein coding intron GSE38233 cultured B-cells chr17:76483003..76483004 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 3 pancreas RMVar_hsa_circ_306022 53125 RMVar_ID_53125 Human_SNP_ID_829599171 A-to-I Human chr17 + 40153931 40153931 40153931 CCTCGTCTCTGCTAAAAATGCAAAAATTAGCCAGCCACTGTGGCACGCGCCTGTAATCCCAGCTA CCTCGTCTCTGCTAAAAATGCAAAAATTAGCCTGCCACTGTGGCACGCGCCTGTAATCCCAGCTA A T CASC3 Ensembl:ENSG00000108349 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr17:40153930..40153931 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_25281371 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 53126 RMVar_ID_53126 Human_SNP_ID_829619445 A-to-I Human chr17 - 82638064 82638064 82638064 CTCGTGCCTCAGCCTTCCAAGTAGCTGGGATTACAGGCACATGCCACCACACCTGGCTACGTTTT CTCGTGCCTCAGCCTTCCAAGTAGCTGGGATTTCAGGCACATGCCACCACACCTGGCTACGTTTT T A WDR45B Ensembl:ENSG00000141580 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr17:82638063..82638064 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - 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 53127 RMVar_ID_53127 Human_SNP_ID_829625633 A-to-I Human chr17 + 4991293 4991293 4991293 GCTTCAAAGCCATCCTAGGCCGCAGGTTGGACAAGCTTGCTTTATACCTCATAGTTAGAGAAGGT GCTTCAAAGCCATCCTAGGCCGCAGGTTGGACGAGCTTGCTTTATACCTCATAGTTAGAGAAGGT A G lnc-KIF1C-1 RNACentral:URS0000D59F3D lincRNA intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr17:4991292..4991293 30559470 RNA-Seq:(High) rs538263160 Functional Loss SNV ICGC 33..33 33 ESCA 1 - 53128 RMVar_ID_53128 Human_SNP_ID_829629228 A-to-I Human chr17 + 28666669 28666669 28666669 TGACTCCCACGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCGTGCA TGACTCCCACGTTCAAGCGATTCTCCTGCCTCGGCCTCCTGAGTAGCTGGGATTACAGGCGTGCA A G SUPT6H Ensembl:ENSG00000109111 Protein coding intron GSE38233 cultured B-cells chr17:28666668..28666669 24183664 RNA-Seq:(High) rs550316422 Functional Loss SNV ICGC 33..33 33 PBCA 1 - 53129 RMVar_ID_53129 Human_SNP_ID_829654889 A-to-I Human chr17 - 34039181 34039181 34039181 AGAAAACAGTAAGAATTCTGACTTAGAGAAGAAGGAGGGAAGAATAGATGATTTATTAAGAGCCA AGAAAACAGTAAGAATTCTGACTTAGAGAAGAGGGAGGGAAGAATAGATGATTTATTAAGAGCCA T C TLK2P1,AC004147.4,AC024610.2,ASIC2 Ensembl:ENSG00000226049,Ensembl:ENSG00000265356,Ensembl:ENSG00000279668,Ensembl:ENSG00000108684 Pseudogene,lincRNA,lincRNA,Protein coding exon,intron,intron,intron GSE100210 HepG2 cell line chr17:34039180..34039181 29129909 RNA-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_3547901 53130 RMVar_ID_53130 Human_SNP_ID_829671457 A-to-I Human chr17 + 80390665 80390665 80390665 ATGATCTGCCCGCTTTGGCCTCTCAAAGTGCTAGAATGAAAAGGCGTGAGCCACTACACCCAGCC ATGATCTGCCCGCTTTGGCCTCTCAAAGTGCTTGAATGAAAAGGCGTGAGCCACTACACCCAGCC A T RNF213 Ensembl:ENSG00000173821 Protein coding intron GSE38233 cultured B-cells chr17:80390664..80390665 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - RMVar_hsa_circ_266998,RMVar_hsa_circ_96925,RMVar_hsa_circ_187517 53131 RMVar_ID_53131 Human_SNP_ID_829686123 A-to-I Human chr17 - 29784475 29784475 29784475 CTCCTGTCTCAGCCTCCCAAGAAGCTGGGATTACAGGCACCCGTCACCACACCCAGCTAATTTTT CTCCTGTCTCAGCCTCCCAAGAAGCTGGGATTGCAGGCACCCGTCACCACACCCAGCTAATTTTT T C SSH2 Ensembl:ENSG00000141298 Protein coding intron GSE100210 HepG2 cell line chr17:29784474..29784475 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - 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 53132 RMVar_ID_53132 Human_SNP_ID_829716798 A-to-I Human chr17 - 43388705 43388705 43388705 TGTCTGGTGTCAGCCTCCTGCCTGGCAGAGGAACTCCAGCCCCTGCTCCCCGAAGCTCCTCCAGG TGTCTGGTGTCAGCCTCCTGCCTGGCAGAGGAGCTCCAGCCCCTGCTCCCCGAAGCTCCTCCAGG T C LINC00910 Ensembl:ENSG00000188825 lincRNA exon GSE100210 HepG2 cell line chr17:43388704..43388705 29129909 RNA-Seq:(High) rs4986155 Functional Loss SNV ICGC 33..33 33 CHOL 1 - Human_RBP_ID_238417,Human_RBP_ID_819647,Human_RBP_ID_2507683,Human_RBP_ID_3547977,Human_RBP_ID_6597470,Human_RBP_ID_8193854,Human_RBP_ID_8453393 53133 RMVar_ID_53133 Human_SNP_ID_829724760 A-to-I Human chr17 - 72844547 72844547 72844547 CTCCTGCCTCGGCCTCTCAAGTGGTTGGGACTACAGGCGCATGCCACGACACCTGGCTACTTTTT CTCCTGCCTCGGCCTCTCAAGTGGTTGGGACTTCAGGCGCATGCCACGACACCTGGCTACTTTTT T A SLC39A11 Ensembl:ENSG00000133195 Protein coding intron GSE100210 HepG2 cell line chr17:72844546..72844547 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_107514,RMVar_hsa_circ_186863,RMVar_hsa_circ_319112 53134 RMVar_ID_53134 Human_SNP_ID_829730001 A-to-I Human chr17 + 63662874 63662874 63662874 GAGATGGGGTTGGGCGGGGGGCGGTCCTCACCATGTTGGCCGGGCTGGTCTCGAACTCTTAAACT GAGATGGGGTTGGGCGGGGGGCGGTCCTCACCTTGTTGGCCGGGCTGGTCTCGAACTCTTAAACT A T MAP3K3 Ensembl:ENSG00000198909 Protein coding intron GSE100210 HepG2 cell line chr17:63662873..63662874 29129909 RNA-Seq:(High) rs1177003092 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 6 liver RMVar_hsa_circ_112584,RMVar_hsa_circ_18458,RMVar_hsa_circ_186319,RMVar_hsa_circ_356624,RMVar_hsa_circ_293103,RMVar_hsa_circ_329400,RMVar_hsa_circ_328761 53135 RMVar_ID_53135 Human_SNP_ID_829735816 A-to-I Human chr17 + 2127511 2127511 2127511 CCCTGCTAAATATTTAATATTATCAAGCTTGTATGACTCAAGCATGGTTTTGGGGCCAGCATCCT CCCTGCTAAATATTTAATATTATCAAGCTTGTGTGACTCAAGCATGGTTTTGGGGCCAGCATCCT A G RF00017-156 RNACentral:URS000091874B SRP RNA intron GSE100210 HepG2 cell line chr17:2127510..2127511 29129909 RNA-Seq:(High) rs879109171 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue 53136 RMVar_ID_53136 Human_SNP_ID_829736588 A-to-I Human chr17 - 57972468 57972468 57972468 CATTATGTGTGGACTACTGGAAGGACTCGTGTAGGGAAAGCCCAAGAATGACCTTGCTGAGGCCT CATTATGTGTGGACTACTGGAAGGACTCGTGTGGGGAAAGCCCAAGAATGACCTTGCTGAGGCCT T C VEZF1 Ensembl:ENSG00000136451 Protein coding 3'UTR GSE38233 cultured B-cells chr17:57972467..57972468 24183664 RNA-Seq:(High) rs11839 Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_495065,Human_RBP_ID_3529815,Human_RBP_ID_4440932,Human_RBP_ID_8458015,Human_RBP_ID_8947857,Human_RBP_ID_13092091,Human_RBP_ID_18703523,Human_RBP_ID_21890235,Human_RBP_ID_23737951,Human_RBP_ID_26453588 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 53137 RMVar_ID_53137 Human_SNP_ID_829747131 A-to-I Human chr17 + 73068167 73068167 73068167 TTGGTGTCGCCAGCAGGTTCCTCTGTTCCCGGAGAAACTGCAGTGGAAGACGGGGGCTCCAGAGT TTGGTGTCGCCAGCAGGTTCCTCTGTTCCCGGGGAAACTGCAGTGGAAGACGGGGGCTCCAGAGT A G - - Other Unknown GSE100210 HepG2 cell line chr17:73068166..73068167 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 8 haematopoietic and lymphoid tissue 53138 RMVar_ID_53138 Human_SNP_ID_829760803 A-to-I Human chr17 + 78203094 78203094 78203094 TTTTTTTTTTTTTTTTTTTGAGACAGAGTCTCACTCTAACCCAGACTGGAACGCAGTGGTGCGAC TTTTTTTTTTTTTTTTTTTGAGACAGAGTCTCTCTCTAACCCAGACTGGAACGCAGTGGTGCGAC A T AFMID Ensembl:ENSG00000183077 Protein coding intron GSE100210 HepG2 cell line chr17:78203093..78203094 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - RMVar_hsa_circ_76228,RMVar_hsa_circ_120249,RMVar_hsa_circ_119104,RMVar_hsa_circ_187322,RMVar_hsa_circ_118921,RMVar_hsa_circ_124317,RMVar_hsa_circ_187326,RMVar_hsa_circ_187327,RMVar_hsa_circ_358459,RMVar_hsa_circ_69193,RMVar_hsa_circ_187328,RMVar_hsa_circ_187330 53139 RMVar_ID_53139 Human_SNP_ID_829773755 A-to-I Human chr17 - 44182846 44182846 44182846 TTGCCCAGGCTGGTCTCAAACTCTAGGACTCAAGTGATCTGCCCCCCTTGGCCTCCCAAAGTGCT TTGCCCAGGCTGGTCTCAAACTCTAGGACTCAGGTGATCTGCCCCCCTTGGCCTCCCAAAGTGCT T C ASB16-AS1 Ensembl:ENSG00000267080 lincRNA intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr17:44182845..44182846 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_1546835,Human_RBP_ID_13022026 RMVar_hsa_circ_99707,RMVar_hsa_circ_184652 53140 RMVar_ID_53140 Human_SNP_ID_829775251 A-to-I Human chr17 + 30069054 30069054 30069054 ACTGCTGTTCTGGATTTCATTGAAGATTACTTAAAAAAAGTGTGTAAACTTTACTCAGAACAAAG ACTGCTGTTCTGGATTTCATTGAAGATTACTTTAAAAAAGTGTGTAAACTTTACTCAGAACAAAG A T AC104996.2,EFCAB5 Ensembl:ENSG00000266876,Ensembl:ENSG00000176927 Pseudogene,Protein coding exon,intron GSE100210 HepG2 cell line chr17:30069053..30069054 29129909 RNA-Seq:(High) rs554582315 Functional Loss SNV ICGC 33..33 33 COCA 1 - 53141 RMVar_ID_53141 Human_SNP_ID_829784547 A-to-I Human chr17 - 76724199 76724199 76724199 GAGAATCACATGAACCTGGGGAAGCAGAGGTTACTGTCAGCCAAGATCACGCCACTGCATTCCAG GAGAATCACATGAACCTGGGGAAGCAGAGGTTGCTGTCAGCCAAGATCACGCCACTGCATTCCAG T C JMJD6 Ensembl:ENSG00000070495 Protein coding intron GSE100210 HepG2 cell line chr17:76724198..76724199 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 5 haematopoietic and lymphoid tissue RMVar_hsa_circ_55438,RMVar_hsa_circ_363283,RMVar_hsa_circ_56844 53142 RMVar_ID_53142 Human_SNP_ID_829807297 A-to-I Human chr17 + 27083559 27083559 27083559 CTATTTGGCCAGTAATAAGTGCTCTCGGGTCTAGGGCATGGGGCTGTCATTGGCTGCTACCACCA CTATTTGGCCAGTAATAAGTGCTCTCGGGTCTGGGGCATGGGGCTGTCATTGGCTGCTACCACCA A G - - Other Unknown GSE100210 HepG2 cell line chr17:27083558..27083559 29129909 RNA-Seq:(High) rs879186451 Functional Loss SNV ICGC 33..33 33 LAML 1 - 53143 RMVar_ID_53143 Human_SNP_ID_829814190 A-to-I Human chr17 - 81630361 81630361 81630361 ATCACTTGAACCTTGGATGTCAAGGCTGCAGTAAGCTGTGATTTTGCCACTGCACTCCAGCCTGG ATCACTTGAACCTTGGATGTCAAGGCTGCAGTGAGCTGTGATTTTGCCACTGCACTCCAGCCTGG T C NPLOC4 Ensembl:ENSG00000182446 Protein coding intron GSE100210 HepG2 cell line chr17:81630360..81630361 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 3 oesophagus Human_RBP_ID_13197891 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 53144 RMVar_ID_53144 Human_SNP_ID_825525281 A-to-I Human chr16 - 57279756 57279756 57279757 AGGTAGGAAGATTGCTTGAGCCTTGGAGTTTAAGGCTGCAGTAAGCCATGATCACGTCACTGCAC AGGTAGGAAGATTGCTTGAGCCTTGGAGTTTGGGGCTGCAGTAAGCCATGATCACGTCACTGCAC TT CC PLLP Ensembl:ENSG00000102934 Protein coding intron GSE47997 K562 cells&HepG2 cells chr16:57279755..57279756 23474544 RNA-Seq:(High) - Functional Loss MNV ICGC 32..33 33 MELA 1 - 53145 RMVar_ID_53145 Human_SNP_ID_825525281 A-to-I Human chr16 - 57279757 57279756 57279757 GAGGTAGGAAGATTGCTTGAGCCTTGGAGTTTAAGGCTGCAGTAAGCCATGATCACGTCACTGCA GAGGTAGGAAGATTGCTTGAGCCTTGGAGTTTGGGGCTGCAGTAAGCCATGATCACGTCACTGCA TT CC PLLP Ensembl:ENSG00000102934 Protein coding intron GSE47997 K562 cells&HepG2 cells chr16:57279756..57279757 23474544 RNA-Seq:(High) - Functional Loss MNV ICGC 33..34 33 MELA 1 - 53146 RMVar_ID_53146 Human_SNP_ID_825546513 A-to-I Human chr16 + 499118 499118 499118 CCTGTAATCCCAGCTACTCAGGAGACTGAGGCAGGAGAATCACCTGAACCCTGGAGGCGGAGCTT CCTGTAATCCCAGCTACTCAGGAGACTGAGGCGGGAGAATCACCTGAACCCTGGAGGCGGAGCTT A G RAB11FIP3 Ensembl:ENSG00000090565 Protein coding intron GSE100210 HepG2 cell line chr16:499117..499118 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 COCA 1 - 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_175367,RMVar_hsa_circ_104952,RMVar_hsa_circ_120827,RMVar_hsa_circ_175366 53147 RMVar_ID_53147 Human_SNP_ID_825574219 A-to-I Human chr16 - 10529848 10529848 10529848 TGGCTCACCGCAACCTCTGCCTCCTGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCT TGGCTCACCGCAACCTCTGCCTCCTGGGTTCAGGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCT T C EMP2 Ensembl:ENSG00000213853 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line chr16:10529847..10529848 31158229,32596459 RNA-Seq:(High) rs1312898312 Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 2 ovary 53148 RMVar_ID_53148 Human_SNP_ID_825602758 A-to-I Human chr16 - 19702758 19702758 19702758 TTGATCTCTTGGCCTCATGATCCACCTACCTCAGCCTCCCAAAGTGTTGGTATTACAGGCATGAG TTGATCTCTTGGCCTCATGATCCACCTACCTCGGCCTCCCAAAGTGTTGGTATTACAGGCATGAG T C KNOP1 Ensembl:ENSG00000103550 Protein coding 3'UTR GSE100210 HepG2 cell line chr16:19702757..19702758 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 53149 RMVar_ID_53149 Human_SNP_ID_825616321 A-to-I Human chr16 - 67681963 67681963 67681963 GTTGTTCAAGCTGGTTTCGAACTCCTAACCTCAGGCAATCATCCTACTTTGGCCCCCCAAAGTGC GTTGTTCAAGCTGGTTTCGAACTCCTAACCTCTGGCAATCATCCTACTTTGGCCCCCCAAAGTGC T A GFOD2 Ensembl:ENSG00000141098 Protein coding intron GSE38233;GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line chr16:67681962..67681963 24183664,29129909,32596459 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_269522 53150 RMVar_ID_53150 Human_SNP_ID_825664143 A-to-I Human chr16 + 69304695 69304695 69304695 TTTTCCTTCTTTTTTTTTTGAGACAGGTTCTCACTCTGTCACCGAGGTTGGAGTGCAGTGGTATG TTTTCCTTCTTTTTTTTTTGAGACAGGTTCTCGCTCTGTCACCGAGGTTGGAGTGCAGTGGTATG A G SNTB2,AC026464.4 Ensembl:ENSG00000168807,Ensembl:ENSG00000260914 Protein coding,Protein coding 3'UTR,intron GSE100210;GSE107867 HepG2 cell line;ASD brains,frontal_cortex chr16:69304694..69304695 29129909,30559470 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue Burkitt_lymphoma 12 haematopoietic and lymphoid tissue Human_RBP_ID_12786967,Human_RBP_ID_23697202 Human_miRNA_ID_866987,Human_miRNA_ID_1793043 53151 RMVar_ID_53151 Human_SNP_ID_825678941 A-to-I Human chr16 - 69316119 69316119 69316119 GCGGCAGCCTGAGGACCCCTCGTGTGACTCACACTTGATAGCGTGGAGGAAGTACTCCACCGCAT GCGGCAGCCTGAGGACCCCTCGTGTGACTCACGCTTGATAGCGTGGAGGAAGTACTCCACCGCAT T C - - Other Unknown GSE38233 cultured B-cells chr16:69316119..69316120 24183664 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 4 stomach 53152 RMVar_ID_53152 Human_SNP_ID_825692467 A-to-I Human chr16 + 48337883 48337866 48337883 TCACCTAGGCTGGATTGCAGTGGCATGATCATAGCTCACTGCAACCTCCACCTCCTGGGCTCCCA TCACCTAGGCTGGATT_________________GCTCACTGCAACCTCCACCTCCTGGGCTCCCA TGCAGTGGCATGATCATA T LONP2 Ensembl:ENSG00000102910 Protein coding intron GSE100210 HepG2 cell line chr16:48337882..48337883 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 17..33 33 OV 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 53153 RMVar_ID_53153 Human_SNP_ID_825695021 A-to-I Human chr16 - 69757008 69757008 69757008 GCCATAAGCACCAGGTCATGCTAATGAGACAGAATTTGATGAGGCGCCAAGAAGAACTTCGGAGG GCCATAAGCACCAGGTCATGCTAATGAGACAGGATTTGATGAGGCGCCAAGAAGAACTTCGGAGG T C AC092115.2 Ensembl:ENSG00000260290 Pseudogene exon GSE100210 HepG2 cell line chr16:69757007..69757008 29129909 RNA-Seq:(High) rs879153615 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_3510790,Human_RBP_ID_5096630,Human_RBP_ID_5274706,Human_RBP_ID_5573259,Human_RBP_ID_6550171,Human_RBP_ID_8252433,Human_RBP_ID_9257151,Human_RBP_ID_17488826,Human_RBP_ID_18513297,Human_RBP_ID_18530310,Human_RBP_ID_26446959 53154 RMVar_ID_53154 Human_SNP_ID_825708127 A-to-I Human chr16 + 67914722 67914722 67914722 GTGATCTGCCCGCCTCAGCTTCCCAAAGTGCTAGGATTACAGGCGTGAGCCACCGCACCCGGTGA GTGATCTGCCCGCCTCAGCTTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCACCCGGTGA A G PSKH1 Ensembl:ENSG00000159792 Protein coding intron GSE100210 HepG2 cell line chr16:67914721..67914722 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 CMDI 1 - 53155 RMVar_ID_53155 Human_SNP_ID_825754830 A-to-I Human chr16 - 19702943 19702943 19702943 ACGCCCAGGCTGGAGTGCAGAGGCGTGATCTCAGCTCACTGCAACCTCCACCTCCAGGGTTCAAG ACGCCCAGGCTGGAGTGCAGAGGCGTGATCTCGGCTCACTGCAACCTCCACCTCCAGGGTTCAAG T C KNOP1 Ensembl:ENSG00000103550 Protein coding 3'UTR GSE100210 HepG2 cell line chr16:19702942..19702943 29129909 RNA-Seq:(High) rs1273729711 Functional Loss SNV ICGC 33..33 33 ESCA 1 - 53156 RMVar_ID_53156 Human_SNP_ID_825770281 A-to-I Human chr16 - 69128916 69128916 69128916 GGGATTACAGGTGAGCGCCACCATGCCTGGCTAATTTTTGTATTTTTCGTAGAAACTGGGTTTCA GGGATTACAGGTGAGCGCCACCATGCCTGGCTGATTTTTGTATTTTTCGTAGAAACTGGGTTTCA T C DERPC,CHTF8 Ensembl:ENSG00000286140,Ensembl:ENSG00000168802 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells chr16:69128915..69128916 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 13 ovary 53157 RMVar_ID_53157 Human_SNP_ID_825804799 A-to-I Human chr16 - 29919446 29919446 29919446 GTTGAAGAGATGATAAGAGTTATAGGTATTCTATGGCACGAATGTAATTACTGGTTCAGGTAAGG GTTGAAGAGATGATAAGAGTTATAGGTATTCTGTGGCACGAATGTAATTACTGGTTCAGGTAAGG T C KCTD13 Ensembl:ENSG00000174943 Protein coding intron GSE100210 HepG2 cell line chr16:29919445..29919446 29129909 RNA-Seq:(High) rs949869639 Functional Loss SNV ICGC 33..33 33 LICA 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,RMVar_hsa_circ_328354,RMVar_hsa_circ_177799 53158 RMVar_ID_53158 Human_SNP_ID_825847719 A-to-I Human chr16 - 74344000 74344000 74344000 CACAAGGTCACGAGATCGAGACCACTCTGGCTAACACAGTGAAACCGCGTCTCTACTAAAAATAC CACAAGGTCACGAGATCGAGACCACTCTGGCTGACACAGTGAAACCGCGTCTCTACTAAAAATAC T C AC009053.2 Ensembl:ENSG00000214331 Pseudogene intron GSE100210 HepG2 cell line chr16:74343999..74344000 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_377905,RMVar_hsa_circ_26233,RMVar_hsa_circ_107349,RMVar_hsa_circ_179924,RMVar_hsa_circ_328760,RMVar_hsa_circ_295646,RMVar_hsa_circ_179928,RMVar_hsa_circ_179927,RMVar_hsa_circ_330711,RMVar_hsa_circ_38169,RMVar_hsa_circ_31970,RMVar_hsa_circ_103025,RMVar_hsa_circ_179930 53159 RMVar_ID_53159 Human_SNP_ID_825852885 A-to-I Human chr16 + 67073517 67073517 67073517 TTGTAATCCCTGCACTCTTGAGAGGCCGAGACAGGTGGATCACTTGAGGTCAGGAGTTCGAGACC TTGTAATCCCTGCACTCTTGAGAGGCCGAGACTGGTGGATCACTTGAGGTCAGGAGTTCGAGACC A T CBFB Ensembl:ENSG00000067955 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr16:67073516..67073517 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 4 liver 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_179022,RMVar_hsa_circ_312067,RMVar_hsa_circ_303452,RMVar_hsa_circ_179023 53160 RMVar_ID_53160 Human_SNP_ID_825853977 A-to-I Human chr16 - 19702736 19702736 19702736 CACCTACCTCAGCCTCCCAAAGTGTTGGTATTACAGGCATGAGCCACCGCACCCAGGCCCCATCA CACCTACCTCAGCCTCCCAAAGTGTTGGTATTGCAGGCATGAGCCACCGCACCCAGGCCCCATCA T C KNOP1 Ensembl:ENSG00000103550 Protein coding 3'UTR GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line chr16:19702735..19702736 29129909,31158229 RNA-Seq:(High) rs1483118316 Functional Loss SNV ICGC 33..33 33 ESCA 1 - 53161 RMVar_ID_53161 Human_SNP_ID_825864085 A-to-I Human chr16 - 75607108 75607108 75607108 ATCTCTCTACAGCCTCGCAAGTAGCTGGGACTACAGATGCCCGCCACCACGCCCAGCTAATTTTT ATCTCTCTACAGCCTCGCAAGTAGCTGGGACTGCAGATGCCCGCCACCACGCCCAGCTAATTTTT T C AC025287.1,ADAT1 Ensembl:ENSG00000259992,Ensembl:ENSG00000065457 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line chr16:75607107..75607108 29129909 RNA-Seq:(High) rs1400121338 Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_22545,RMVar_hsa_circ_267048,RMVar_hsa_circ_323654,RMVar_hsa_circ_180075,RMVar_hsa_circ_272488,RMVar_hsa_circ_180076,RMVar_hsa_circ_180077 53162 RMVar_ID_53162 Human_SNP_ID_825865388 A-to-I Human chr16 + 89549508 89549508 89549508 CAGCAAGACCCCATCTCTTAAAAGAAAAGAATAAAGAGTATTAGCCAGGCATGGTGGTGGAGCAC CAGCAAGACCCCATCTCTTAAAAGAAAAGAATGAAGAGTATTAGCCAGGCATGGTGGTGGAGCAC A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line chr16:89549507..89549508;chr16:89549508..89549509 31158229 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 10 haematopoietic and lymphoid tissue Human_RBP_ID_22207855 Human_Splice_Rec_1752618 RMVar_hsa_circ_29778,RMVar_hsa_circ_112642,RMVar_hsa_circ_180624,RMVar_hsa_circ_35388,RMVar_hsa_circ_106819,RMVar_hsa_circ_180626,RMVar_hsa_circ_306711,RMVar_hsa_circ_93099,RMVar_hsa_circ_180634,RMVar_hsa_circ_275214,RMVar_hsa_circ_114472,RMVar_hsa_circ_180637,RMVar_hsa_circ_306888,RMVar_hsa_circ_180640,RMVar_hsa_circ_103409,RMVar_hsa_circ_180642,RMVar_hsa_circ_180643 53163 RMVar_ID_53163 Human_SNP_ID_825894854 A-to-I Human chr16 - 11893397 11893397 11893397 TACTTGGCTGGGCATGGTGGCTCATATCTGTAATCCTAGCATTTTGGGAGGCCAAGGCGGAAGGA TACTTGGCTGGGCATGGTGGCTCATATCTGTACTCCTAGCATTTTGGGAGGCCAAGGCGGAAGGA T G GSPT1 Ensembl:ENSG00000103342 Protein coding intron GSE38233 cultured B-cells chr16:11893396..11893397 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 9 pancreas RMVar_hsa_circ_265911,RMVar_hsa_circ_290007,RMVar_hsa_circ_299414,RMVar_hsa_circ_346910,RMVar_hsa_circ_57970,RMVar_hsa_circ_176336,RMVar_hsa_circ_267294,RMVar_hsa_circ_378391,RMVar_hsa_circ_33614,RMVar_hsa_circ_44188,RMVar_hsa_circ_123824,RMVar_hsa_circ_122966,RMVar_hsa_circ_301376,RMVar_hsa_circ_296866,RMVar_hsa_circ_59894,RMVar_hsa_circ_176338,RMVar_hsa_circ_176339,RMVar_hsa_circ_176337,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_369412,RMVar_hsa_circ_322195,RMVar_hsa_circ_176348,RMVar_hsa_circ_176349,RMVar_hsa_circ_118833,RMVar_hsa_circ_176350,RMVar_hsa_circ_375603,RMVar_hsa_circ_176353,RMVar_hsa_circ_55711,RMVar_hsa_circ_124627,RMVar_hsa_circ_176352,RMVar_hsa_circ_352421,RMVar_hsa_circ_117900,RMVar_hsa_circ_176354 53164 RMVar_ID_53164 Human_SNP_ID_825919176 A-to-I Human chr16 + 7155388 7155388 7155388 GAGTTCAGTGGGTCACTTAAGCCAGGAGTTCAAAACCAGCCTGGGATACATGGAAAAACTCCATA GAGTTCAGTGGGTCACTTAAGCCAGGAGTTCACAACCAGCCTGGGATACATGGAAAAACTCCATA A C RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr16:7155388..7155389 30559470 RNA-Seq:(High) rs961371699 Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_12201 53165 RMVar_ID_53165 Human_SNP_ID_825927035 A-to-I Human chr16 - 89812291 89812291 89812291 CTCTGTCGCCCAGACTGCAGTGTAGTGGCGTGATCTCGGCTCACTGCAAACTCCGCCTCCTGGGT CTCTGTCGCCCAGACTGCAGTGTAGTGGCGTGTTCTCGGCTCACTGCAAACTCCGCCTCCTGGGT T A FANCA Ensembl:ENSG00000187741 Protein coding intron GSE38233 cultured B-cells chr16:89812290..89812291 24183664 RNA-Seq:(High) rs1295891291 Functional Loss SNV ICGC 33..33 33 PRAD 1 - Human_RBP_ID_12861018 RMVar_hsa_circ_180690,RMVar_hsa_circ_124924,RMVar_hsa_circ_57797,RMVar_hsa_circ_100923,RMVar_hsa_circ_180744,RMVar_hsa_circ_128184,RMVar_hsa_circ_180754,RMVar_hsa_circ_3215,RMVar_hsa_circ_103412,RMVar_hsa_circ_180758,RMVar_hsa_circ_377504,RMVar_hsa_circ_325343 53166 RMVar_ID_53166 Human_SNP_ID_825931695 A-to-I Human chr16 + 15701026 15701026 15701026 GGAAGGCCGAGGCGGGTGGATTACCTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGGTGA GGAAGGCCGAGGCGGGTGGATTACCTGAGGTCCGGAGTTCAAGACCAGCCTGGCCAACATGGTGA A C NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr16:15701025..15701026 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 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 53167 RMVar_ID_53167 Human_SNP_ID_825944187 A-to-I Human chr16 + 29697029 29697029 29697029 CGGTGCGGGCGGCCAGACAGGCGGCTGACTTCACTCTGAAGGTGGAAGTGGAATGCAGCAGCCTG CGGTGCGGGCGGCCAGACAGGCGGCTGACTTCGCTCTGAAGGTGGAAGTGGAATGCAGCAGCCTG A G QPRT Ensembl:ENSG00000103485 Protein coding CDS GSE100210 HepG2 cell line chr16:29697028..29697029 29129909 RNA-Seq:(High) rs9932770 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,COCA 7 head and neck Human_RBP_ID_889606,Human_RBP_ID_9353194,Human_RBP_ID_21889201,Human_RBP_ID_22442464 Human_Splice_Rec_1699788,Human_Splice_Rec_1699789,Human_Splice_Rec_1699792,Human_Splice_Rec_1699793,Human_Splice_Rec_1699798,Human_Splice_Rec_1699799,Human_Splice_Rec_1699804,Human_Splice_Rec_1699805 53168 RMVar_ID_53168 Human_SNP_ID_825973377 A-to-I Human chr16 + 1755753 1755753 1755753 CCTGTAATCCCAGCTACTCAGAAGACTAAGGCAAGTGAATCGCTTGAACCCGAGACGTGGAGGTT CCTGTAATCCCAGCTACTCAGAAGACTAAGGCGAGTGAATCGCTTGAACCCGAGACGTGGAGGTT A G MAPK8IP3 Ensembl:ENSG00000138834 Protein coding intron GSE100210 HepG2 cell line chr16:1755753..1755754 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BOCA 1 - 53169 RMVar_ID_53169 Human_SNP_ID_825985339 A-to-I Human chr16 + 28961269 28961269 28961269 AGGATCGCTTGTGCCTAGGAGATTGAGGCTGCAGTGAGCTGAGATTGGGCCACTGCACTCCAGCC AGGATCGCTTGTGCCTAGGAGATTGAGGCTGCGGTGAGCTGAGATTGGGCCACTGCACTCCAGCC A G NFATC2IP Ensembl:ENSG00000176953 Protein coding intron GSE100210 HepG2 cell line chr16:28961268..28961269 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_25204067 RMVar_hsa_circ_91884,RMVar_hsa_circ_177698 53170 RMVar_ID_53170 Human_SNP_ID_825991232 A-to-I Human chr16 - 23520030 23520030 23520030 GTGGATCAGGCTGGTCTCAAACTGCCGACCTCAGGTGATCCGCCTGCCTCGGCCTCCCAAAGGGC GTGGATCAGGCTGGTCTCAAACTGCCGACCTCCGGTGATCCGCCTGCCTCGGCCTCCCAAAGGGC T G GGA2 Ensembl:ENSG00000103365 Protein coding intron GSE100210 HepG2 cell line chr16:23520029..23520030 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - 53171 RMVar_ID_53171 Human_SNP_ID_826027271 A-to-I Human chr16 - 67477837 67477837 67477837 AACCCCGTCTCTACTAAAAATACAAAAAAATTAGCCTTGTGTGGTGGCGGGTGCCTGTAGTCCCA AACCCCGTCTCTACTAAAAATACAAAAAAATTTGCCTTGTGTGGTGGCGGGTGCCTGTAGTCCCA T A ATP6V0D1 Ensembl:ENSG00000159720 Protein coding intron GSE100210 HepG2 cell line chr16:67477836..67477837 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 4 oesophagus RMVar_hsa_circ_85319,RMVar_hsa_circ_117044,RMVar_hsa_circ_179078,RMVar_hsa_circ_179082 53172 RMVar_ID_53172 Human_SNP_ID_826046554 A-to-I Human chr16 + 31040913 31040913 31040913 CAGAGGCTGAGGTGGGAGGATCGCTTGAGCCCAGGAGATTAAGGCTGCAGTGAGCCATGGTCATC CAGAGGCTGAGGTGGGAGGATCGCTTGAGCCCGGGAGATTAAGGCTGCAGTGAGCCATGGTCATC A G STX4 Ensembl:ENSG00000103496 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line chr16:31040912..31040913 31158229 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 1 - 53173 RMVar_ID_53173 Human_SNP_ID_826048760 A-to-I Human chr16 - 10531136 10531136 10531136 AACCCCGTCTCTACCGAAAATACAACAAAATTAGCCCGGTGTGGTGGCAGGTGCCTGTAATCCCA AACCCCGTCTCTACCGAAAATACAACAAAATTGGCCCGGTGTGGTGGCAGGTGCCTGTAATCCCA T C EMP2 Ensembl:ENSG00000213853 Protein coding 3'UTR GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line chr16:10531135..10531136 29129909,32596459 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 53174 RMVar_ID_53174 Human_SNP_ID_826050951 A-to-I Human chr16 - 21138702 21138702 21138702 GGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCAACTGCCACCATG GGGTTCAAGTGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCAACTGCCACCATG T C DNAH3 Ensembl:ENSG00000158486 Protein coding intron GSE47997 K562 cells&HepG2 cells chr16:21138701..21138702 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_49740 53175 RMVar_ID_53175 Human_SNP_ID_826087567 A-to-I Human chr16 + 79017247 79017247 79017247 GGTCAGAAGTTGGAGACCATCCTGGCTAACACAGTGAAACCCCATATCTCCTAAAAATACAAAAA GGTCAGAAGTTGGAGACCATCCTGGCTAACACGGTGAAACCCCATATCTCCTAAAAATACAAAAA A G WWOX,AC009145.4 Ensembl:ENSG00000186153,Ensembl:ENSG00000280274 Protein coding,Other intron,exon GSE47997 K562 cells&HepG2 cells chr16:79017246..79017247 23474544 RNA-Seq:(High) rs570188356 Functional Loss SNV ICGC 33..33 33 LICA 1 - 53176 RMVar_ID_53176 Human_SNP_ID_826088314 A-to-I Human chr16 + 72278330 72278330 72278330 CGTGAGCAGTTCCGGAGGTACTTGGAGAAGTCAGGGGTGCTGGACACACTGACCAAGGTGTTGGT CGTGAGCAGTTCCGGAGGTACTTGGAGAAGTCGGGGGTGCTGGACACACTGACCAAGGTGTTGGT A G AC009075.2 Ensembl:ENSG00000261774 Pseudogene exon GSE100210 HepG2 cell line chr16:72278329..72278330 29129909 RNA-Seq:(High) rs1405766077 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_5573414 53177 RMVar_ID_53177 Human_SNP_ID_826096595 A-to-I Human chr16 + 74299525 74299525 74299525 CCTCAGTCCCCCAGCCCCAAGTAGCTGAGACTACAGGCACATCCCCACTATGCCCGGCTAAGTTT CCTCAGTCCCCCAGCCCCAAGTAGCTGAGACTGCAGGCACATCCCCACTATGCCCGGCTAAGTTT A G PSMD7 Ensembl:ENSG00000103035 Protein coding intron GSE100210 HepG2 cell line chr16:74299524..74299525 29129909 RNA-Seq:(High) rs1315058150 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue Human_RBP_ID_6536272 RMVar_hsa_circ_179910,RMVar_hsa_circ_89829 53178 RMVar_ID_53178 Human_SNP_ID_826107911 A-to-I Human chr16 + 69622856 69622856 69622856 TTGTTTGGGAAAAAAAAAAAAAAGAAAAAAATAGACTCGAGGCTGGGTGTGGTGGCTCACGCCTG TTGTTTGGGAAAAAAAAAAAAAAGAAAAAAATTGACTCGAGGCTGGGTGTGGTGGCTCACGCCTG A T NFAT5 Ensembl:ENSG00000102908 Protein coding intron GSE100210 HepG2 cell line chr16:69622855..69622856 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 7 breast RMVar_hsa_circ_179419,RMVar_hsa_circ_86768,RMVar_hsa_circ_350666,RMVar_hsa_circ_90611,RMVar_hsa_circ_179415,RMVar_hsa_circ_179416,RMVar_hsa_circ_179417,RMVar_hsa_circ_179418 53179 RMVar_ID_53179 Human_SNP_ID_826153388 A-to-I Human chr16 - 16679 16679 16679 GACCTGGGCCAGGTGCCTGAGATTGATGTTCCATCCTACCTGCCTGACCTGCCCGGCATTGCCAA GACCTGGGCCAGGTGCCTGAGATTGATGTTCCGTCCTACCTGCCTGACCTGCCCGGCATTGCCAA T C WASH4P Ensembl:ENSG00000234769 Pseudogene exon GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank chr16:16678..16679 30559470 RNA-Seq:(High) rs575317242 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_Splice_Rec_1652204 53180 RMVar_ID_53180 Human_SNP_ID_826169226 A-to-I Human chr16 - 4349691 4349691 4349691 GCGATCCTAGCTCACTGCAGCCTTGAACTCCTAGGCTCAAGCCATCCTCCTACCTTAGACCCCCA GCGATCCTAGCTCACTGCAGCCTTGAACTCCTCGGCTCAAGCCATCCTCCTACCTTAGACCCCCA T G PAM16,CORO7-PAM16 Ensembl:ENSG00000217930,Ensembl:ENSG00000103426 Protein coding,Protein coding intron,intron GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490829,GSM3490830,GSM3490831 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,EC109 cell line chr16:4349690..4349691 24183664,29129909,29796672,31158229,32596459 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 5 breast RMVar_hsa_circ_77031,RMVar_hsa_circ_123394,RMVar_hsa_circ_119552,RMVar_hsa_circ_175984,RMVar_hsa_circ_175985,RMVar_hsa_circ_175983 53181 RMVar_ID_53181 Human_SNP_ID_826181870 A-to-I Human chr16 + 487913 487913 487913 ACGGCGCCCCCCAGTGGTTGTGTGAGGACAGCAGCTCCCTAGGGAAGAGGCAGAGGTGCTTGAAC ACGGCGCCCCCCAGTGGTTGTGTGAGGACAGCGGCTCCCTAGGGAAGAGGCAGAGGTGCTTGAAC A G RAB11FIP3 Ensembl:ENSG00000090565 Protein coding intron GSE38233 cultured B-cells chr16:487912..487913 24183664 RNA-Seq:(High) rs2385130 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_12753784,Human_RBP_ID_18437833 GWAS_ID_1230,GWAS_ID_1231,GWAS_ID_1232,GWAS_ID_1233,GWAS_ID_1234,GWAS_ID_1235,GWAS_ID_1236 RMVar_hsa_circ_175356,RMVar_hsa_circ_103523,RMVar_hsa_circ_294420,RMVar_hsa_circ_175355,RMVar_hsa_circ_294492,RMVar_hsa_circ_269225,RMVar_hsa_circ_122699,RMVar_hsa_circ_125620,RMVar_hsa_circ_355032,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_320314,RMVar_hsa_circ_334611,RMVar_hsa_circ_272740,RMVar_hsa_circ_175363,RMVar_hsa_circ_175364,RMVar_hsa_circ_175362 53182 RMVar_ID_53182 Human_SNP_ID_826184789 A-to-I Human chr16 + 28963061 28963061 28963061 AAACTTAGCTGGGTGTGGTGGCCTGTGCCTGTAGTTGCAGCTACTCAGGAGGCTGAGGCAGGAGA AAACTTAGCTGGGTGTGGTGGCCTGTGCCTGTTGTTGCAGCTACTCAGGAGGCTGAGGCAGGAGA A T NFATC2IP Ensembl:ENSG00000176953 Protein coding intron GSE38233 cultured B-cells chr16:28963060..28963061 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_91884,RMVar_hsa_circ_177698 53183 RMVar_ID_53183 Human_SNP_ID_826193183 A-to-I Human chr16 + 79017465 79017463 79017465 AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAGAAAGAAATTACAGGTAGGCTAGAGCACGGA AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAG__AGAAAGAAATTACAGGTAGGCTAGAGCACGGA GAA G WWOX Ensembl:ENSG00000186153 Protein coding intron GSE47997 K562 cells&HepG2 cells chr16:79017465..79017466 23474544 RNA-Seq:(High) - Functional Loss DEL ICGC 32..33 33 CHOL 1 - 53184 RMVar_ID_53184 Human_SNP_ID_826193838 A-to-I Human chr16 - 58569560 58569560 58569560 CTTTTTCTGTTTGGTATGTTGTAGAGTGTAGTATCTGATGGGAAAAAACGAATTTCTGTTTTTTG CTTTTTCTGTTTGGTATGTTGTAGAGTGTAGTGTCTGATGGGAAAAAACGAATTTCTGTTTTTTG T C CNOT1 Ensembl:ENSG00000125107 Protein coding intron GSE38233 cultured B-cells chr16:58569559..58569560 24183664 RNA-Seq:(High) rs7192054 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_1089706,Human_RBP_ID_6523877,Human_RBP_ID_12766305,Human_RBP_ID_23694414,Human_RBP_ID_27659439 GWAS_ID_4327,GWAS_ID_4328 RMVar_hsa_circ_4429,RMVar_hsa_circ_84121,RMVar_hsa_circ_83986,RMVar_hsa_circ_119739,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_119415,RMVar_hsa_circ_178776,RMVar_hsa_circ_114456,RMVar_hsa_circ_178783,RMVar_hsa_circ_372807,RMVar_hsa_circ_361850,RMVar_hsa_circ_178786,RMVar_hsa_circ_128166,RMVar_hsa_circ_178790,RMVar_hsa_circ_88886,RMVar_hsa_circ_178791,RMVar_hsa_circ_376794,RMVar_hsa_circ_81146,RMVar_hsa_circ_103931,RMVar_hsa_circ_178796,RMVar_hsa_circ_178798,RMVar_hsa_circ_178802,RMVar_hsa_circ_51306,RMVar_hsa_circ_115468,RMVar_hsa_circ_178804,RMVar_hsa_circ_93835,RMVar_hsa_circ_178803,RMVar_hsa_circ_75924,RMVar_hsa_circ_107527,RMVar_hsa_circ_86057,RMVar_hsa_circ_178809,RMVar_hsa_circ_178810,RMVar_hsa_circ_178808,RMVar_hsa_circ_109818,RMVar_hsa_circ_178812,RMVar_hsa_circ_86089,RMVar_hsa_circ_178814,RMVar_hsa_circ_110381,RMVar_hsa_circ_73537,RMVar_hsa_circ_178817,RMVar_hsa_circ_356645,RMVar_hsa_circ_121420,RMVar_hsa_circ_178821,RMVar_hsa_circ_178823,RMVar_hsa_circ_51761,RMVar_hsa_circ_178822,RMVar_hsa_circ_60582,RMVar_hsa_circ_103073,RMVar_hsa_circ_51046,RMVar_hsa_circ_83523,RMVar_hsa_circ_178825,RMVar_hsa_circ_60317,RMVar_hsa_circ_112367,RMVar_hsa_circ_55810,RMVar_hsa_circ_57253,RMVar_hsa_circ_38766,RMVar_hsa_circ_178839,RMVar_hsa_circ_87340,RMVar_hsa_circ_97750,RMVar_hsa_circ_116657,RMVar_hsa_circ_178828,RMVar_hsa_circ_178830,RMVar_hsa_circ_178829,RMVar_hsa_circ_178827,RMVar_hsa_circ_360983,RMVar_hsa_circ_123305,RMVar_hsa_circ_114267,RMVar_hsa_circ_115165,RMVar_hsa_circ_108140,RMVar_hsa_circ_95481,RMVar_hsa_circ_96016,RMVar_hsa_circ_92019,RMVar_hsa_circ_79703,RMVar_hsa_circ_82762,RMVar_hsa_circ_84450,RMVar_hsa_circ_80784,RMVar_hsa_circ_178843,RMVar_hsa_circ_178847,RMVar_hsa_circ_178849,RMVar_hsa_circ_78836,RMVar_hsa_circ_178850,RMVar_hsa_circ_178848,RMVar_hsa_circ_178845,RMVar_hsa_circ_178846,RMVar_hsa_circ_178844,RMVar_hsa_circ_178841,RMVar_hsa_circ_178840,RMVar_hsa_circ_178835,RMVar_hsa_circ_178837,RMVar_hsa_circ_178838,RMVar_hsa_circ_178836,RMVar_hsa_circ_178834 53185 RMVar_ID_53185 Human_SNP_ID_826205023 A-to-I Human chr16 + 29670421 29670421 29670421 TGAGGCAGAAGAATTGCTTGAAACCGGGAGGCAGAGGTTGCAGTGAGCCGAGATCGTGTCATTGC TGAGGCAGAAGAATTGCTTGAAACCGGGAGGCGGAGGTTGCAGTGAGCCGAGATCGTGTCATTGC A G SPN,QPRT Ensembl:ENSG00000197471,Ensembl:ENSG00000103485 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells chr16:29670420..29670421 24183664 RNA-Seq:(High) rs779771534 Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 3 breast Human_RBP_ID_17564654 53186 RMVar_ID_53186 Human_SNP_ID_826206725 A-to-I Human chr16 - 18348003 18348003 18348003 CCCTGCCTCCCTCTCCACAGGTCACCCTCCACAGCCAGGATGTCCTCATGCTCCCTGGTGACCTC CCCTGCCTCCCTCTCCACAGGTCACCCTCCACGGCCAGGATGTCCTCATGCTCCCTGGTGACCTC T C AC126755.1 Ensembl:ENSG00000205746 Pseudogene exon GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank chr16:18348002..18348003 30559470 RNA-Seq:(High) rs1258051131 Functional Loss SNV TCGA 33..33 33 SARC,UCEC,CESC 4 - Human_RBP_ID_5690,Human_RBP_ID_760323,Human_RBP_ID_816232,Human_RBP_ID_891608,Human_RBP_ID_3510545,Human_RBP_ID_3947368,Human_RBP_ID_5088025,Human_RBP_ID_5183221,Human_RBP_ID_5524100,Human_RBP_ID_5572885,Human_RBP_ID_8188622,Human_RBP_ID_8726977,Human_RBP_ID_9257211,Human_RBP_ID_9286562,Human_RBP_ID_9421919,Human_RBP_ID_9841653,Human_RBP_ID_17079113,Human_RBP_ID_17257623,Human_RBP_ID_17372491,Human_RBP_ID_17488507,Human_RBP_ID_17565321,Human_RBP_ID_17608109,Human_RBP_ID_17884475,Human_RBP_ID_18163818,Human_RBP_ID_18486220,Human_RBP_ID_18940877,Human_RBP_ID_18983313,Human_RBP_ID_19071018,Human_RBP_ID_21973926,Human_RBP_ID_22357077,Human_RBP_ID_22370541,Human_RBP_ID_22425571,Human_RBP_ID_22541330,Human_RBP_ID_22653939,Human_RBP_ID_22738826,Human_RBP_ID_27837802 Human_Splice_Rec_1684318 RMVar_hsa_circ_83046,RMVar_hsa_circ_176753,RMVar_hsa_circ_102126,RMVar_hsa_circ_176754 53187 RMVar_ID_53187 Human_SNP_ID_826236919 A-to-I Human chr16 - 18847835 18847835 18847835 CAGCAAAATTGTAGATAAGCTGTCCTCTGCAAACCCCACCATGGTATTACAGGTACAAAGAAACT CAGCAAAATTGTAGATAAGCTGTCCTCTGCAAGCCCCACCATGGTATTACAGGTACAAAGAAACT T C SMG1 Ensembl:ENSG00000157106 Protein coding CDS GSE100210 HepG2 cell line chr16:18847834..18847835 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC 33..33 33 BLCA 2 - Human_RBP_ID_469490,Human_RBP_ID_1838911,Human_RBP_ID_3947386,Human_RBP_ID_5524169,Human_RBP_ID_8231573,Human_RBP_ID_8805124,Human_RBP_ID_9372385,Human_RBP_ID_17872563,Human_RBP_ID_19073590,Human_RBP_ID_21888785 Human_Splice_Rec_1685255,Human_Splice_Rec_1685371,Human_Splice_Rec_1685431 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_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_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_280366,RMVar_hsa_circ_116579,RMVar_hsa_circ_267701,RMVar_hsa_circ_327588,RMVar_hsa_circ_106160,RMVar_hsa_circ_33831,RMVar_hsa_circ_176846,RMVar_hsa_circ_176848,RMVar_hsa_circ_176849,RMVar_hsa_circ_176847,RMVar_hsa_circ_44453,RMVar_hsa_circ_372613,RMVar_hsa_circ_176850 53188 RMVar_ID_53188 Human_SNP_ID_826244480 A-to-I Human chr16 + 66890109 66890109 66890109 TGAGACCAGCCTGACCAACATGGTAAAACTCCATCTCTACTAAAAATACAAAAATTAGCCTGGAA TGAGACCAGCCTGACCAACATGGTAAAACTCCCTCTCTACTAAAAATACAAAAATTAGCCTGGAA A C PDP2 Ensembl:ENSG00000172840 Protein coding 3'UTR GSE47997;GSE38233;GSE99789;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;cultured B-cells;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BERP35T4 cell line chr16:66890108..66890109 23474544,24183664,29796672,31158229 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 RECA 1 - Human_RBP_ID_127314 RMVar_hsa_circ_90756,RMVar_hsa_circ_178998 53189 RMVar_ID_53189 Human_SNP_ID_826257838 A-to-I Human chr16 - 5028840 5028840 5028840 CGTGAGAGCCGCCTTCGTGAGGGCTGAAGTCCAGGTCTGCCCCAGCCTGTCTCATTCAGCCAATA CGTGAGAGCCGCCTTCGTGAGGGCTGAAGTCCGGGTCTGCCCCAGCCTGTCTCATTCAGCCAATA T C NAGPA Ensembl:ENSG00000103174 Protein coding intron GSE100210 HepG2 cell line chr16:5028839..5028840 29129909 RNA-Seq:(High) rs1995278 Functional Loss SNV ICGC 33..33 33 COCA 5 - Human_RBP_ID_19070822 RMVar_hsa_circ_52592,RMVar_hsa_circ_354914,RMVar_hsa_circ_176086 53190 RMVar_ID_53190 Human_SNP_ID_826271431 A-to-I Human chr16 + 57206765 57206765 57206765 TTAAAAAAGTTTTTGTAGAGCCAGGTCTTGCCATGTTGCCCAGGCTGGTCTCAAATACCTGGACT TTAAAAAAGTTTTTGTAGAGCCAGGTCTTGCCTTGTTGCCCAGGCTGGTCTCAAATACCTGGACT A T RSPRY1 Ensembl:ENSG00000159579 Protein coding intron GSE100210 HepG2 cell line chr16:57206764..57206765 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - RMVar_hsa_circ_14462,RMVar_hsa_circ_347477,RMVar_hsa_circ_372792,RMVar_hsa_circ_275680,RMVar_hsa_circ_330545,RMVar_hsa_circ_14508,RMVar_hsa_circ_178683,RMVar_hsa_circ_178684,RMVar_hsa_circ_178685,RMVar_hsa_circ_178682 53191 RMVar_ID_53191 Human_SNP_ID_826288300 A-to-I Human chr16 - 70250424 70250424 70250424 CCTCAGGTGATCCACCCGCCTTGGCCTCCCAAAGTGCTGGAATTACAGGTGTGAGCCACTGTGCC CCTCAGGTGATCCACCCGCCTTGGCCTCCCAAGGTGCTGGAATTACAGGTGTGAGCCACTGTGCC T C EXOSC6 Ensembl:ENSG00000223496 Protein coding 3'UTR GSE100210 HepG2 cell line chr16:70250423..70250424 29129909 RNA-Seq:(High) rs1405951945 Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_4380622,Human_RBP_ID_25224777 53192 RMVar_ID_53192 Human_SNP_ID_826305241 A-to-I Human chr16 - 18817956 18817956 18817956 TTAAGGCTACAGTGAGCCATAATTAAGCCACTATACTCCAGCCTGGGCAACAGGGGAGACCTTGT TTAAGGCTACAGTGAGCCATAATTAAGCCACTGTACTCCAGCCTGGGCAACAGGGGAGACCTTGT T C SMG1 Ensembl:ENSG00000157106 Protein coding intron GSE38233 cultured B-cells chr16:18817955..18817956 24183664 RNA-Seq:(High) rs924334004 Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_3052,RMVar_hsa_circ_103304,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_176790,RMVar_hsa_circ_84851,RMVar_hsa_circ_115830,RMVar_hsa_circ_282686,RMVar_hsa_circ_330548,RMVar_hsa_circ_176794,RMVar_hsa_circ_364098,RMVar_hsa_circ_272407,RMVar_hsa_circ_72297,RMVar_hsa_circ_74302,RMVar_hsa_circ_68176,RMVar_hsa_circ_176795,RMVar_hsa_circ_176797,RMVar_hsa_circ_176799,RMVar_hsa_circ_176798,RMVar_hsa_circ_176796,RMVar_hsa_circ_69843,RMVar_hsa_circ_64506,RMVar_hsa_circ_269768,RMVar_hsa_circ_267825 53193 RMVar_ID_53193 Human_SNP_ID_826312968 A-to-I Human chr16 + 2938880 2938880 2938880 GTGATCCGCCTGTCTTGGCCTCCCAAAGTGCTAGGATTACAGGCGTGAGTCACTGTGCCCAACCT GTGATCCGCCTGTCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGTCACTGTGCCCAACCT A G FLYWCH1 Ensembl:ENSG00000059122 Protein coding intron GSE100210 HepG2 cell line chr16:2938879..2938880 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 3 liver 53194 RMVar_ID_53194 Human_SNP_ID_826313818 A-to-I Human chr16 - 23465859 23465859 23465859 TCAGCTCACTGCAATCTCTGCCTACCAGGTTCAAGCGATTCTCGTGCCTCAGCCTCTCGAGTAGC TCAGCTCACTGCAATCTCTGCCTACCAGGTTCGAGCGATTCTCGTGCCTCAGCCTCTCGAGTAGC T C GGA2 Ensembl:ENSG00000103365 Protein coding 3'UTR GSE100210 HepG2 cell line chr16:23465858..23465859 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 3 ovary Human_RBP_ID_26439956 53195 RMVar_ID_53195 Human_SNP_ID_826354781 A-to-I Human chr16 - 24920155 24920155 24920155 CGTGCCTGGCCGCATCCTGCTGGATATAGACAATGATACCGAGAGCACTGCCCTGTGAAGAAAGC CGTGCCTGGCCGCATCCTGCTGGATATAGACAGTGATACCGAGAGCACTGCCCTGTGAAGAAAGC T C ARHGAP17 Ensembl:ENSG00000140750 Protein coding exon GSE100210 HepG2 cell line chr16:24920154..24920155 29129909 RNA-Seq:(High) rs759941236 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_RBP_ID_893413,Human_RBP_ID_1840295,Human_RBP_ID_5097411,Human_RBP_ID_6550143,Human_RBP_ID_8188657,Human_RBP_ID_17257050,Human_RBP_ID_17673267,Human_RBP_ID_17884417,Human_RBP_ID_19077453,Human_RBP_ID_21973529 Human_Splice_Rec_1693724 Human_miRNA_ID_1860653,Human_miRNA_ID_1861097,Human_miRNA_ID_1875155,Human_miRNA_ID_1875435 53196 RMVar_ID_53196 Human_SNP_ID_826370549 A-to-I Human chr16 + 68154050 68154050 68154050 GCAGCCCTCCCACCTCAGCCTTCTAAGTAGCTAGGACTACAGGAGCACACCACCATGCTCAGCTA GCAGCCCTCCCACCTCAGCCTTCTAAGTAGCTTGGACTACAGGAGCACACCACCATGCTCAGCTA A T NFATC3 Ensembl:ENSG00000072736 Protein coding intron GSE100210 HepG2 cell line chr16:68154049..68154050 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_179205,RMVar_hsa_circ_286210,RMVar_hsa_circ_179198,RMVar_hsa_circ_294649,RMVar_hsa_circ_296020,RMVar_hsa_circ_343271,RMVar_hsa_circ_291835,RMVar_hsa_circ_281495,RMVar_hsa_circ_179201,RMVar_hsa_circ_179203,RMVar_hsa_circ_179204,RMVar_hsa_circ_179202,RMVar_hsa_circ_356013,RMVar_hsa_circ_361959,RMVar_hsa_circ_179206,RMVar_hsa_circ_361224,RMVar_hsa_circ_327647,RMVar_hsa_circ_179208 53197 RMVar_ID_53197 Human_SNP_ID_826379684 A-to-I Human chr16 - 57177749 57177749 57177749 CCTTGGCCTCCCAAAGTGTTGGGATTATAGGCATGAGCCACCATGCCCAGCCTGAATTAAGATAT CCTTGGCCTCCCAAAGTGTTGGGATTATAGGCGTGAGCCACCATGCCCAGCCTGAATTAAGATAT T C PSME3IP1 Ensembl:ENSG00000172775 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr16:57177748..57177749 24183664,29129909 RNA-Seq:(High) rs1490153172 Functional Loss SNV ICGC 33..33 33 RECA 1 - RMVar_hsa_circ_178678,RMVar_hsa_circ_77293,RMVar_hsa_circ_54715,RMVar_hsa_circ_34406 53198 RMVar_ID_53198 Human_SNP_ID_826391217 A-to-I Human chr16 + 3272240 3272240 3272240 AGGCATGGTGGCACGTGCCTGTAGTCTCAGCTACTCGCGAGGCTGAGGCAGAAGAATTGCTTGAA AGGCATGGTGGCACGTGCCTGTAGTCTCAGCTGCTCGCGAGGCTGAGGCAGAAGAATTGCTTGAA A G ZNF263 Ensembl:ENSG00000006194 Protein coding intron GSE100210 HepG2 cell line chr16:3272239..3272240 29129909 RNA-Seq:(High) rs1394343033 Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 3 ovary 53199 RMVar_ID_53199 Human_SNP_ID_826410367 A-to-I Human chr16 + 6788628 6788628 6788628 CTCCCGAGTAGCTGGAACTACAGGTGCCTACGACCATGCCCAGCTGATTGTTTGTATTTTTAGTA CTCCCGAGTAGCTGGAACTACAGGTGCCTACGTCCATGCCCAGCTGATTGTTTGTATTTTTAGTA A T RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE107867 ASD brains,cerebellum chr16:6788627..6788628 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma,CLLE 9 haematopoietic and lymphoid tissue RMVar_hsa_circ_12201 53200 RMVar_ID_53200 Human_SNP_ID_826420210 A-to-I Human chr16 + 682558 682558 682558 GCCCTGGGCAGAAGCCCCCGGCCCCTATACATAGTTTATGTTCCTGGCCACCCCGACCGCTTCCC GCCCTGGGCAGAAGCCCCCGGCCCCTATACATTGTTTATGTTCCTGGCCACCCCGACCGCTTCCC A T STUB1 Ensembl:ENSG00000103266 Protein coding 3'UTR GSE100210 HepG2 cell line chr16:682557..682558 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_277697,Human_RBP_ID_479316,Human_RBP_ID_1005482,Human_RBP_ID_1846371,Human_RBP_ID_23699661 Human_miRNA_ID_2576618,Human_miRNA_ID_3088724 RMVar_hsa_circ_120706,RMVar_hsa_circ_126165,RMVar_hsa_circ_175418,RMVar_hsa_circ_175420 53201 RMVar_ID_53201 Human_SNP_ID_826440716 A-to-I Human chr16 - 74947286 74947286 74947286 GTGCCACCATGCCCGGCTAATTTTGTATTTTTAGTAAAGATGGGGTTTCTCCACGTTGGTCAAGC GTGCCACCATGCCCGGCTAATTTTGTATTTTTTGTAAAGATGGGGTTTCTCCACGTTGGTCAAGC T A WDR59 Ensembl:ENSG00000103091 Protein coding intron GSE100210 HepG2 cell line chr16:74947285..74947286 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - RMVar_hsa_circ_373,RMVar_hsa_circ_8447,RMVar_hsa_circ_180006,RMVar_hsa_circ_90270,RMVar_hsa_circ_348093,RMVar_hsa_circ_115136,RMVar_hsa_circ_180016,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_120143,RMVar_hsa_circ_180033,RMVar_hsa_circ_2684,RMVar_hsa_circ_180034,RMVar_hsa_circ_274537,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,RMVar_hsa_circ_180045,RMVar_hsa_circ_305790,RMVar_hsa_circ_370224,RMVar_hsa_circ_302741,RMVar_hsa_circ_180044 53202 RMVar_ID_53202 Human_SNP_ID_826475578 A-to-I Human chr16 + 67240340 67240340 67240340 CCTAAGGTCAGGAGTTCTAGACCAGCCTGGCCAACGTGGTGAAACCCCGTCTCTACAAAAATGCA CCTAAGGTCAGGAGTTCTAGACCAGCCTGGCCTACGTGGTGAAACCCCGTCTCTACAAAAATGCA A T SLC9A5 Ensembl:ENSG00000135740 Protein coding intron GSE100210 HepG2 cell line chr16:67240340..67240341 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 53203 RMVar_ID_53203 Human_SNP_ID_826502344 A-to-I Human chr16 + 15408921 15408921 15408921 ATTCTGCGTCAGCCTCCCAAGTAGCTGGGACTACAGGCACCTGCCACGATGCCTAGCTAATTTTT ATTCTGCGTCAGCCTCCCAAGTAGCTGGGACTGCAGGCACCTGCCACGATGCCTAGCTAATTTTT A G MPV17L,AC140504.1 Ensembl:ENSG00000156968,Ensembl:ENSG00000261130 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line chr16:15408920..15408921 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 2 oesophagus 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_103195,RMVar_hsa_circ_93945,RMVar_hsa_circ_84522,RMVar_hsa_circ_176538,RMVar_hsa_circ_176539,RMVar_hsa_circ_176540 53204 RMVar_ID_53204 Human_SNP_ID_826504057 A-to-I Human chr16 + 24854461 24854461 24854461 AGTTTTTTTTTTTTTTCCGGAGACAGAGTCTCACTCTGTCCCCCAGGCTGGAGTGCAGTGGCATA AGTTTTTTTTTTTTTTCCGGAGACAGAGTCTCCCTCTGTCCCCCAGGCTGGAGTGCAGTGGCATA A C SLC5A11 Ensembl:ENSG00000158865 Protein coding intron GSE100210 HepG2 cell line chr16:24854460..24854461 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 STAD 1 - RMVar_hsa_circ_342277 53205 RMVar_ID_53205 Human_SNP_ID_826504236 A-to-I Human chr16 - 20310824 20310824 20310824 CGAACTCAGGGGGTGGAGGTTGCAGTGAGTTGAGATTGTGCCATTGCACTCCAGCCTGGGCAACA CGAACTCAGGGGGTGGAGGTTGCAGTGAGTTGGGATTGTGCCATTGCACTCCAGCCTGGGCAACA T C GP2 Ensembl:ENSG00000169347 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells chr16:20310823..20310824 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - 53206 RMVar_ID_53206 Human_SNP_ID_826542755 A-to-I Human chr16 + 89498330 89498330 89498330 AAACTCCTGGGCTCACTCAACCCTCCTGCCTCAGCCTCCCAAAGTATTAAGATCACAGGCATAAG AAACTCCTGGGCTCACTCAACCCTCCTGCCTCTGCCTCCCAAAGTATTAAGATCACAGGCATAAG A T SPG7 Ensembl:ENSG00000197912 Protein coding exon GSE100210 HepG2 cell line chr16:89498329..89498330 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 53207 RMVar_ID_53207 Human_SNP_ID_826586669 A-to-I Human chr16 + 24572297 24572297 24572297 GGAAAAGAAAAAACACAAGAAACATAAAAAGCATAAGAAGCATAAGAAACATGCAGGCACTGAAG GGAAAAGAAAAAACACAAGAAACATAAAAAGCGTAAGAAGCATAAGAAACATGCAGGCACTGAAG A G RBBP6 Ensembl:ENSG00000122257 Protein coding CDS GSE47997 K562 cells&HepG2 cells chr16:24572296..24572297 23474544 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 5 liver Human_RBP_ID_1526959,Human_RBP_ID_4358080,Human_RBP_ID_9444025,Human_RBP_ID_22198684,Human_RBP_ID_24544397 53208 RMVar_ID_53208 Human_SNP_ID_826664549 A-to-I Human chr16 - 31568945 31568945 31568945 CCGTTACAGACGTGGCTACTATGGAAGGCGCCATGGCCCTCCCCGGGATTACGCTGGGAGGAGGA CCGTTACAGACGTGGCTACTATGGAAGGCGCCGTGGCCCTCCCCGGGATTACGCTGGGAGGAGGA T C YBX3P1 Ensembl:ENSG00000261614 Pseudogene exon GSE100210 HepG2 cell line chr16:31568944..31568945 29129909 RNA-Seq:(High) rs968989121 Functional Loss SNV ICGC 33..33 33 LAML 1 - 53209 RMVar_ID_53209 Human_SNP_ID_826702972 A-to-I Human chr16 - 18324472 18324472 18324472 TCCTAGGTGTCTTTCCTGAAGACTATCTTCCCATCTCAAAATGGACATGATGGATCCACGGATGT TCCTAGGTGTCTTTCCTGAAGACTATCTTCCCGTCTCAAAATGGACATGATGGATCCACGGATGT T C NPIPA8,AC126755.7 Ensembl:ENSG00000214940,Ensembl:ENSG00000285628 Protein coding,lincRNA CDS,exon GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank chr16:18324471..18324472 30559470 RNA-Seq:(High) rs750188546 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_Splice_Rec_1684226,Human_Splice_Rec_1684227,Human_Splice_Rec_1684240,Human_Splice_Rec_1684241,Human_Splice_Rec_1684290,Human_Splice_Rec_1684291 53210 RMVar_ID_53210 Human_SNP_ID_826714867 A-to-I Human chr16 + 15015077 15015077 15015077 CTCCCGCCTCGGCCCCGCGAGTACCTGGGACTATAGGCGCCCACCACTACACCCGGCTAATTTTG CTCCCGCCTCGGCCCCGCGAGTACCTGGGACTGTAGGCGCCCACCACTACACCCGGCTAATTTTG A G PDXDC1 Ensembl:ENSG00000179889 Protein coding intron GSE100210 HepG2 cell line chr16:15015076..15015077 29129909 RNA-Seq:(High) rs192812417 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 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_125777,RMVar_hsa_circ_176498,RMVar_hsa_circ_5646,RMVar_hsa_circ_69488,RMVar_hsa_circ_321402,RMVar_hsa_circ_346116,RMVar_hsa_circ_82502,RMVar_hsa_circ_39291,RMVar_hsa_circ_176503,RMVar_hsa_circ_176504 53211 RMVar_ID_53211 Human_SNP_ID_826722060 A-to-I Human chr16 + 68003700 68003700 68003700 CATTCATTCAGGATCAAGTCCAAGTATCTCTGACCATACCTTATTTCCTTGTCTTTGAGGCCAAA CATTCATTCAGGATCAAGTCCAAGTATCTCTGGCCATACCTTATTTCCTTGTCTTTGAGGCCAAA A G DUS2 Ensembl:ENSG00000167264 Protein coding intron GSE100210 HepG2 cell line chr16:68003699..68003700 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 2 - 53212 RMVar_ID_53212 Human_SNP_ID_826724407 A-to-I Human chr16 + 74299483 74299483 74299483 CTAGCCTCAAACTCGACCTTCTGAGCTCAAGTAGTCCCTGCACCTCAGTCCCCCAGCCCCAAGTA CTAGCCTCAAACTCGACCTTCTGAGCTCAAGTGGTCCCTGCACCTCAGTCCCCCAGCCCCAAGTA A G PSMD7 Ensembl:ENSG00000103035 Protein coding intron GSE38233 cultured B-cells chr16:74299482..74299483 24183664 RNA-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_6536271,Human_RBP_ID_12808240 RMVar_hsa_circ_179910,RMVar_hsa_circ_89829 53213 RMVar_ID_53213 Human_SNP_ID_826773823 A-to-I Human chr16 + 75041902 75041902 75041902 CCTATAATCCCAGCTACTCGGGAGCCTGAGGCAGGAGAATCACTTGAACCTGGGAGACGGAGGTC CCTATAATCCCAGCTACTCGGGAGCCTGAGGCTGGAGAATCACTTGAACCTGGGAGACGGAGGTC A T ZNRF1 Ensembl:ENSG00000186187 Protein coding intron GSE100210 HepG2 cell line chr16:75041901..75041902 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_17564324,Human_RBP_ID_22715417 53214 RMVar_ID_53214 Human_SNP_ID_826839959 A-to-I Human chr16 - 75446009 75446009 75446009 CACCGTGCCCGGCTAATTTTTGTATTTTTAGTAGAGATAGGTTTCACCATCTTGCCCAGGCTGGT CACCGTGCCCGGCTAATTTTTGTATTTTTAGTGGAGATAGGTTTCACCATCTTGCCCAGGCTGGT T C AC009163.5,TMEM170A Ensembl:ENSG00000261717,Ensembl:ENSG00000166822 Protein coding,Protein coding intron,3'UTR GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line chr16:75446008..75446009 24183664,29129909,29796672,31158229,31158229,31158229,32596459 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 53215 RMVar_ID_53215 Human_SNP_ID_826840046 A-to-I Human chr16 + 89549430 89549430 89549430 GCCTGTAATCCCAGCACTTTGGGGGCTGAGGCAGGAGGGTTGCTTGAGGCCAGGAGTTTGAGACC GCCTGTAATCCCAGCACTTTGGGGGCTGAGGCGGGAGGGTTGCTTGAGGCCAGGAGTTTGAGACC A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line chr16:89549429..89549430 31158229,32596459 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 10 haematopoietic and lymphoid tissue Human_RBP_ID_22652595 RMVar_hsa_circ_29778,RMVar_hsa_circ_112642,RMVar_hsa_circ_180624,RMVar_hsa_circ_35388,RMVar_hsa_circ_106819,RMVar_hsa_circ_180626,RMVar_hsa_circ_306711,RMVar_hsa_circ_93099,RMVar_hsa_circ_180634,RMVar_hsa_circ_275214,RMVar_hsa_circ_114472,RMVar_hsa_circ_180637,RMVar_hsa_circ_306888,RMVar_hsa_circ_180640,RMVar_hsa_circ_103409,RMVar_hsa_circ_180642,RMVar_hsa_circ_180643 53216 RMVar_ID_53216 Human_SNP_ID_826845815 A-to-I Human chr16 - 57182762 57182762 57182762 GGGATTACAGGCATGTGCTACTACGCCTGGCTAATTTTCATATTTTTAGTAGAGACGGAGTTTCA GGGATTACAGGCATGTGCTACTACGCCTGGCTCATTTTCATATTTTTAGTAGAGACGGAGTTTCA T G PSME3IP1 Ensembl:ENSG00000172775 Protein coding intron GSE100210 HepG2 cell line chr16:57182761..57182762 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_6522289 RMVar_hsa_circ_178678,RMVar_hsa_circ_77293 53217 RMVar_ID_53217 Human_SNP_ID_826848130 A-to-I Human chr16 - 46608342 46608342 46608342 CATTTGGAGGAGTTGGGATGAAGAAGAGGAGGATGAATACGATTATTTTGTCAGATGTGTTGAAC CATTTGGAGGAGTTGGGATGAAGAAGAGGAGGGTGAATACGATTATTTTGTCAGATGTGTTGAAC T C SHCBP1 Ensembl:ENSG00000171241 Protein coding CDS GSE47997 K562 cells&HepG2 cells chr16:46608341..46608342 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 NACA 1 - Human_RBP_ID_888714,Human_RBP_ID_1842598,Human_RBP_ID_3949166,Human_RBP_ID_4400502,Human_RBP_ID_6513549,Human_RBP_ID_9345640,Human_RBP_ID_22654210,Human_RBP_ID_22939442 Human_Splice_Rec_1707902,Human_Splice_Rec_1707903,Human_Splice_Rec_1707928,Human_Splice_Rec_1707929,Human_Splice_Rec_1707942,Human_Splice_Rec_1707943,Human_Splice_Rec_1707948,Human_Splice_Rec_1707949 RMVar_hsa_circ_3159,RMVar_hsa_circ_57712,RMVar_hsa_circ_362364,RMVar_hsa_circ_347009,RMVar_hsa_circ_4165,RMVar_hsa_circ_304816,RMVar_hsa_circ_65929 53218 RMVar_ID_53218 Human_SNP_ID_826866234 A-to-I Human chr16 + 19648715 19648715 19648715 TATGGTGAAATGCTGTCTCTACTAAAAATACCAAAGTTAGTCAGGCGGGGTGGCAGGCACCTGTT TATGGTGAAATGCTGTCTCTACTAAAAATACCGAAGTTAGTCAGGCGGGGTGGCAGGCACCTGTT A G VPS35L Ensembl:ENSG00000103544 Protein coding intron GSE38233 cultured B-cells chr16:19648715..19648716 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 7 prostate RMVar_hsa_circ_377326,RMVar_hsa_circ_104887,RMVar_hsa_circ_89821,RMVar_hsa_circ_284533,RMVar_hsa_circ_10393,RMVar_hsa_circ_176923,RMVar_hsa_circ_85709,RMVar_hsa_circ_369450,RMVar_hsa_circ_287757,RMVar_hsa_circ_176925,RMVar_hsa_circ_176926,RMVar_hsa_circ_287430,RMVar_hsa_circ_124672,RMVar_hsa_circ_273723,RMVar_hsa_circ_176932,RMVar_hsa_circ_176933,RMVar_hsa_circ_176928,RMVar_hsa_circ_176930,RMVar_hsa_circ_176931,RMVar_hsa_circ_176929,RMVar_hsa_circ_18908,RMVar_hsa_circ_30805,RMVar_hsa_circ_16385,RMVar_hsa_circ_321996,RMVar_hsa_circ_176946,RMVar_hsa_circ_344504,RMVar_hsa_circ_176950,RMVar_hsa_circ_176951,RMVar_hsa_circ_176954,RMVar_hsa_circ_25052,RMVar_hsa_circ_337162,RMVar_hsa_circ_300765,RMVar_hsa_circ_278485,RMVar_hsa_circ_176955,RMVar_hsa_circ_176952,RMVar_hsa_circ_176953,RMVar_hsa_circ_61486,RMVar_hsa_circ_86215,RMVar_hsa_circ_283684,RMVar_hsa_circ_176962,RMVar_hsa_circ_310172,RMVar_hsa_circ_330114,RMVar_hsa_circ_176963,RMVar_hsa_circ_297710,RMVar_hsa_circ_315233,RMVar_hsa_circ_283128,RMVar_hsa_circ_96039,RMVar_hsa_circ_176965,RMVar_hsa_circ_176967,RMVar_hsa_circ_176966,RMVar_hsa_circ_176971,RMVar_hsa_circ_176964,RMVar_hsa_circ_176972,RMVar_hsa_circ_366129,RMVar_hsa_circ_284755,RMVar_hsa_circ_314118,RMVar_hsa_circ_280174,RMVar_hsa_circ_42626,RMVar_hsa_circ_176974,RMVar_hsa_circ_176976,RMVar_hsa_circ_176975,RMVar_hsa_circ_176973,RMVar_hsa_circ_359633,RMVar_hsa_circ_289543,RMVar_hsa_circ_176979 53219 RMVar_ID_53219 Human_SNP_ID_826882604 A-to-I Human chr16 + 29669660 29669660 29669660 CCAGCACTTTGGGAGGCCGAGGCAGGTGGATCACCTGAGGTCAGGAGTTCAAGACCAGCCTGACC CCAGCACTTTGGGAGGCCGAGGCAGGTGGATCGCCTGAGGTCAGGAGTTCAAGACCAGCCTGACC A G SPN,QPRT Ensembl:ENSG00000197471,Ensembl:ENSG00000103485 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells chr16:29669659..29669660 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 COCA 1 - 53220 RMVar_ID_53220 Human_SNP_ID_826936399 A-to-I Human chr16 - 8853869 8853869 8853869 GTTGGGCAGGATGGTCTTGAACCCCTGACCTCAGATGATCTGCCCATCTCGGCCTCTCAAAGTGC GTTGGGCAGGATGGTCTTGAACCCCTGACCTCGGATGATCTGCCCATCTCGGCCTCTCAAAGTGC T C CARHSP1 Ensembl:ENSG00000153048 Protein coding 3'UTR GSE38233 cultured B-cells chr16:8853868..8853869 24183664 RNA-Seq:(High) rs764882927 Functional Loss SNV ICGC 33..33 33 MELA 1 - 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 53221 RMVar_ID_53221 Human_SNP_ID_826981517 A-to-I Human chr16 + 6717989 6717989 6717989 ATAAATTCTGTAGGTGGCCTTCTCTCCCCTGCACCATTTTCTACCACCACCACCGTCATCACCAC ATAAATTCTGTAGGTGGCCTTCTCTCCCCTGCTCCATTTTCTACCACCACCACCGTCATCACCAC A T RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE107867 ASD brains,cerebellum chr16:6717988..6717989 30559470 RNA-Seq:(High) rs1184931258 Functional Loss SNV ICGC 33..33 33 RECA 1 - RMVar_hsa_circ_12201 53222 RMVar_ID_53222 Human_SNP_ID_826993280 A-to-I Human chr16 - 19701590 19701590 19701590 TGCCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAATCACCGTGCCCGGCCAATAAAT TGCCTGCCTCAGCCTCCCAAAGTGCTGGGATTGCAGGCGTGAATCACCGTGCCCGGCCAATAAAT T C - - Other Unknown GSE100210 HepG2 cell line chr16:19701589..19701590 29129909 RNA-Seq:(High) rs529118881 Functional Loss SNV ICGC 33..33 33 ESCA 1 - 53223 RMVar_ID_53223 Human_SNP_ID_827018786 A-to-I Human chr16 - 30581843 30581843 30581843 GACCTCGTGATCCACCCGCCTCGGCGTCTCAAAGTGCTGGGATTACAAGCGTGAGCCACCGACCC GACCTCGTGATCCACCCGCCTCGGCGTCTCAAGGTGCTGGGATTACAAGCGTGAGCCACCGACCC T C ZNF785 Ensembl:ENSG00000197162 Protein coding intron GSE100210 HepG2 cell line chr16:30581842..30581843 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - 53224 RMVar_ID_53224 Human_SNP_ID_827019009 A-to-I Human chr16 - 111717 111717 111717 TGGCTGCGGTGGCTCATGCCTGTAATCCCAGCACTTAGGGAGGCTGAGGCAGGTAGATTGCTTGA TGGCTGCGGTGGCTCATGCCTGTAATCCCAGCCCTTAGGGAGGCTGAGGCAGGTAGATTGCTTGA T G NPRL3 Ensembl:ENSG00000103148 Protein coding intron GSE38233 cultured B-cells chr16:111716..111717 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LMS 1 - RMVar_hsa_circ_23515,RMVar_hsa_circ_41368,RMVar_hsa_circ_18523,RMVar_hsa_circ_340681,RMVar_hsa_circ_31031,RMVar_hsa_circ_303011,RMVar_hsa_circ_15605,RMVar_hsa_circ_310544,RMVar_hsa_circ_337813 53225 RMVar_ID_53225 Human_SNP_ID_827030650 A-to-I Human chr16 - 19704190 19704190 19704190 TAATCCCGGCTACTCAGGAGGCTGACAGGAGAATCGCTTGAACCCGGGAGGTGGAGGTTGTAGTG TAATCCCGGCTACTCAGGAGGCTGACAGGAGAGTCGCTTGAACCCGGGAGGTGGAGGTTGTAGTG T C KNOP1 Ensembl:ENSG00000103550 Protein coding 3'UTR GSE38233 cultured B-cells chr16:19704189..19704190 24183664 RNA-Seq:(High) rs138873958 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_17564020,Human_RBP_ID_27439681 53226 RMVar_ID_53226 Human_SNP_ID_827035648 A-to-I Human chr16 + 56907364 56907362 56907365 CCTGTAATCCCAGCTACTTGGGAGGCTGAGACAGGAGAATTGCTTGAACCTGGGAGGCAGAGGTT CCTGTAATCCCAGCTACTTGGGAGGCTGAGA___GAGAATTGCTTGAACCTGGGAGGCAGAGGTT ACAG A SLC12A3 Ensembl:ENSG00000070915 Protein coding intron GSE100210 HepG2 cell line chr16:56907363..56907364 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 32..34 33 LMS 1 - RMVar_hsa_circ_127714,RMVar_hsa_circ_178621 53227 RMVar_ID_53227 Human_SNP_ID_827076915 A-to-I Human chr16 - 16324932 16324932 16324932 GCTGCTCCCCCTACGCAGGCCTGCACTCACCCATGCATTCGAAGTGCACCTTGGTGGTGAGAGCG GCTGCTCCCCCTACGCAGGCCTGCACTCACCCGTGCATTCGAAGTGCACCTTGGTGGTGAGAGCG T C lnc-ABCC6-5 RNACentral:URS00009C1DDA lincRNA exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr16:16324931..16324932 30559470 RNA-Seq:(High) rs558042008 Functional Loss SNV ICGC 33..33 33 LUSC 1 - 53228 RMVar_ID_53228 Human_SNP_ID_827090926 A-to-I Human chr16 - 15363876 15363876 15363876 GCGTCTGCTCTATCCCCTTCCACCCTCAGCGGATGATAATCTCAAGACACCTCCCGAGTGTCTGC GCGTCTGCTCTATCCCCTTCCACCCTCAGCGGTTGATAATCTCAAGACACCTCCCGAGTGTCTGC T A NPIPA5 Ensembl:ENSG00000183793 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr16:15363875..15363876 30559470 RNA-Seq:(High) rs752982027 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 head_neck squamous_cell_carcinoma,LIHC,liver hepatocellular_carcinoma 4 liver,head and neck Human_RBP_ID_22053940,Human_RBP_ID_22935931 53229 RMVar_ID_53229 Human_SNP_ID_827125681 A-to-I Human chr16 - 15711830 15711830 15711830 AAATTAGCCGGGTATGGTGGGGCGTGCCTGTAATCCCAGCTACTAGGGAGGCTGAGGCAGGAGAA AAATTAGCCGGGTATGGTGGGGCGTGCCTGTAGTCCCAGCTACTAGGGAGGCTGAGGCAGGAGAA T C MYH11 Ensembl:ENSG00000133392 Protein coding intron GSE100210 HepG2 cell line chr16:15711829..15711830 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 53230 RMVar_ID_53230 Human_SNP_ID_827125877 A-to-I Human chr16 - 18786282 18786282 18786282 TTGGCTACTGCAACCTCTGTCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCTAGTAGCT TTGGCTACTGCAACCTCTGTCTCCCAGGTTCACGCGATTCTCCTGCCTCAGCCTCCCTAGTAGCT T G RPS15A Ensembl:ENSG00000134419 Protein coding intron GSE100210 HepG2 cell line chr16:18786281..18786282 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 UCEC 1 - Human_RBP_ID_12679197 Human_Splice_Rec_1685072,Human_Splice_Rec_1685073,Human_Splice_Rec_1685096,Human_Splice_Rec_1685097 RMVar_hsa_circ_122283,RMVar_hsa_circ_176773,RMVar_hsa_circ_77194,RMVar_hsa_circ_176774,RMVar_hsa_circ_112033,RMVar_hsa_circ_176775,RMVar_hsa_circ_176777,RMVar_hsa_circ_375183 53231 RMVar_ID_53231 Human_SNP_ID_827126302 A-to-I Human chr16 + 15698063 15698063 15698063 TGACATTGTGATCCACCCACCTCGGCCTCTCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCAA TGACATTGTGATCCACCCACCTCGGCCTCTCAGAGTGCTGGGATTACAGGCGTGAGCCACTGCAA A G NDE1 Ensembl:ENSG00000072864 Protein coding intron GSE100210 HepG2 cell line chr16:15698063..15698064 29129909 RNA-Seq:(High) rs1032745740 Functional Loss SNV ICGC 33..33 33 LICA 1 - 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,RMVar_hsa_circ_36726 53232 RMVar_ID_53232 Human_SNP_ID_827189391 A-to-I Human chr16 + 10924467 10924467 10924467 GTTGGCCAGGCTGGTCTCAAACTCTTGACCTCAGGTGATCCACCCACCTCAGCCTCCCAAAGTGC GTTGGCCAGGCTGGTCTCAAACTCTTGACCTCGGGTGATCCACCCACCTCAGCCTCCCAAAGTGC A G CIITA Ensembl:ENSG00000179583 Protein coding 3'UTR GSE38233 cultured B-cells chr16:10924466..10924467 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - 53233 RMVar_ID_53233 Human_SNP_ID_827190077 A-to-I Human chr16 + 28957942 28957942 28957942 ATCACCTGAGGTCAGGAGTTCGAGACCAGCCTAGCCAACATGGTGAAACCCCATCTCTACTAAAA ATCACCTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAA A G NFATC2IP Ensembl:ENSG00000176953 Protein coding intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line chr16:28957941..28957942 24183664,31158229 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 2 prostate RMVar_hsa_circ_78324,RMVar_hsa_circ_177693,RMVar_hsa_circ_336064,RMVar_hsa_circ_285448,RMVar_hsa_circ_177694,RMVar_hsa_circ_177695 53234 RMVar_ID_53234 Human_SNP_ID_827258399 A-to-I Human chr16 - 88567089 88567089 88567089 TTGCCCAGGCTGGTCTCAAACTCTGGGCCTCAAGCGATCCTCCCACCTTGGCCTTCCAAAGTGCT TTGCCCAGGCTGGTCTCAAACTCTGGGCCTCAGGCGATCCTCCCACCTTGGCCTTCCAAAGTGCT T C ZC3H18-AS1,lnc-CYBA-4 RNACentral:URS0000D577BC,RNACentral:URS0000D57635 lincRNA,lincRNA exon,intron GSE100210 HepG2 cell line chr16:88567088..88567089 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - 53235 RMVar_ID_53235 Human_SNP_ID_827258532 A-to-I Human chr16 + 16329208 16329208 16329208 GCCACCTCACCGCCTTCGGCACCAGCCTCTTCATGCCCCCAAGCCATGTACGCTTTGTGTTTCCT GCCACCTCACCGCCTTCGGCACCAGCCTCTTCGTGCCCCCAAGCCATGTACGCTTTGTGTTTCCT A G AC138969.1,PKD1P1 Ensembl:ENSG00000183889,Ensembl:ENSG00000244257 Protein coding,Pseudogene exon,exon GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank;ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr16:16329207..16329208 30559470 RNA-Seq:(High) rs3883137 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_8941715,Human_RBP_ID_17673332,Human_RBP_ID_21959961 Human_Splice_Rec_1683893,Human_Splice_Rec_1683957 Human_miRNA_ID_1826406,Human_miRNA_ID_1826608 53236 RMVar_ID_53236 Human_SNP_ID_827311467 A-to-I Human chr16 + 22212508 22212508 22212508 CACCACACCCAGCTGGTTTTTGTATTTTTAGTAGAGATGGGGTTTTCACCATGTTGGTCAGGTCT CACCACACCCAGCTGGTTTTTGTATTTTTAGTGGAGATGGGGTTTTCACCATGTTGGTCAGGTCT A G EEF2K Ensembl:ENSG00000103319 Protein coding intron GSE100210 HepG2 cell line chr16:22212507..22212508 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_177156,RMVar_hsa_circ_81910 53237 RMVar_ID_53237 Human_SNP_ID_827318614 A-to-I Human chr16 - 19704196 19704196 19704196 GGCTTGTAATCCCGGCTACTCAGGAGGCTGACAGGAGAATCGCTTGAACCCGGGAGGTGGAGGTT GGCTTGTAATCCCGGCTACTCAGGAGGCTGACGGGAGAATCGCTTGAACCCGGGAGGTGGAGGTT T C KNOP1 Ensembl:ENSG00000103550 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr16:19704195..19704196 24183664,29129909 RNA-Seq:(High) rs1166188382 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_6497979,Human_RBP_ID_17564020,Human_RBP_ID_17872806 53238 RMVar_ID_53238 Human_SNP_ID_827321750 A-to-I Human chr16 - 69757035 69757035 69757035 AGCCAGAGATGGAGATGGAGGCTGCACGCCATAAGCACCAGGTCATGCTAATGAGACAGAATTTG AGCCAGAGATGGAGATGGAGGCTGCACGCCATGAGCACCAGGTCATGCTAATGAGACAGAATTTG T C AC092115.2 Ensembl:ENSG00000260290 Pseudogene exon GSE100210 HepG2 cell line chr16:69757034..69757035 29129909 RNA-Seq:(High) rs879127181 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_5573259 53239 RMVar_ID_53239 Human_SNP_ID_827345159 A-to-I Human chr16 + 7195583 7195583 7195583 TTATTTATTTGTTTGTTTATTTATTGAGACAGAGTCCAACTCTCTTGCCCAGGCTGGAGTGCAGT TTATTTATTTGTTTGTTTATTTATTGAGACAGGGTCCAACTCTCTTGCCCAGGCTGGAGTGCAGT A G RBFOX1 Ensembl:ENSG00000078328 Protein coding intron GSE107867 ASD brains,cerebellum chr16:7195582..7195583 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - RMVar_hsa_circ_12201 53240 RMVar_ID_53240 Human_SNP_ID_827348248 A-to-I Human chr16 + 29696621 29696621 29696621 TGGCCACCATGGTGAAACGTCGTCTCTATTAAAAATACAAAAATTAGCTGGGCATGGTGGCACGC TGGCCACCATGGTGAAACGTCGTCTCTATTAATAATACAAAAATTAGCTGGGCATGGTGGCACGC A T QPRT Ensembl:ENSG00000103485 Protein coding intron GSE47997 K562 cells&HepG2 cells chr16:29696621..29696622 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 53241 RMVar_ID_53241 Human_SNP_ID_827373139 A-to-I Human chr16 - 70378959 70378959 70378959 GAGTCTTGTTCTGTTACCCAGGCTGGAGTGCAATGGCCCGATGTCGGCTCATCCCAACCTCCACC GAGTCTTGTTCTGTTACCCAGGCTGGAGTGCAGTGGCCCGATGTCGGCTCATCCCAACCTCCACC T C ST3GAL2 Ensembl:ENSG00000157350 Protein coding 3'UTR GSE38233 cultured B-cells chr16:70378958..70378959 24183664 RNA-Seq:(High) rs117025305 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_2481406,Human_RBP_ID_12796337,Human_RBP_ID_23165224,Human_RBP_ID_25225347 Human_miRNA_ID_1075396 53242 RMVar_ID_53242 Human_SNP_ID_827388102 A-to-I Human chr16 + 54395253 54395253 54395253 ACTTTGGGATTCCATAACAAAAATTGTAGACTAGATGTCTCAAACAACATAAATTTACTTTCTTA ACTTTGGGATTCCATAACAAAAATTGTAGACTGGATGTCTCAAACAACATAAATTTACTTTCTTA A G - - Other Unknown GSE100210 HepG2 cell line chr16:54395252..54395253 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 53243 RMVar_ID_53243 Human_SNP_ID_827392112 A-to-I Human chr16 + 70575993 70575993 70575993 AATCCCAGCACTTTGGGCGGCCAGAGGCAGGCAGATTGCTTGAGCCCAGAAGTTTAAGACCAGCC AATCCCAGCACTTTGGGCGGCCAGAGGCAGGCGGATTGCTTGAGCCCAGAAGTTTAAGACCAGCC A G SF3B3 Ensembl:ENSG00000189091 Protein coding 3'UTR GSE107867 ASD brains,cerebellum;ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr16:70575992..70575993 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_6532891,Human_RBP_ID_12799392 RMVar_hsa_circ_121582,RMVar_hsa_circ_179639,RMVar_hsa_circ_83258,RMVar_hsa_circ_179640,RMVar_hsa_circ_86802,RMVar_hsa_circ_179663,RMVar_hsa_circ_123867,RMVar_hsa_circ_179680,RMVar_hsa_circ_94340,RMVar_hsa_circ_179681,RMVar_hsa_circ_103993,RMVar_hsa_circ_124047,RMVar_hsa_circ_179702,RMVar_hsa_circ_179703 53244 RMVar_ID_53244 Human_SNP_ID_827397958 A-to-I Human chr16 + 30485802 30485802 30485802 GCAATCTGCCCACCTCGGCCTCCTAAAGTGCTAGGATTACAGGCGTGAGCCACTGCACCCGGCCC GCAATCTGCCCACCTCGGCCTCCTAAAGTGCTGGGATTACAGGCGTGAGCCACTGCACCCGGCCC A G ITGAL Ensembl:ENSG00000005844 Protein coding intron GSE38233 cultured B-cells chr16:30485801..30485802 24183664 RNA-Seq:(High) rs543243610 Functional Loss SNV ICGC 33..33 33 BOCA 1 - RMVar_hsa_circ_86007,RMVar_hsa_circ_98934,RMVar_hsa_circ_177881,RMVar_hsa_circ_369439,RMVar_hsa_circ_177882,RMVar_hsa_circ_17761,RMVar_hsa_circ_87381,RMVar_hsa_circ_107545,RMVar_hsa_circ_177883,RMVar_hsa_circ_177885,RMVar_hsa_circ_127884,RMVar_hsa_circ_177889,RMVar_hsa_circ_177887,RMVar_hsa_circ_177888,RMVar_hsa_circ_92051,RMVar_hsa_circ_59739,RMVar_hsa_circ_350310,RMVar_hsa_circ_355696,RMVar_hsa_circ_18399,RMVar_hsa_circ_81430,RMVar_hsa_circ_2195,RMVar_hsa_circ_177891 53245 RMVar_ID_53245 Human_SNP_ID_827427527 A-to-I Human chr16 + 29669068 29669068 29669068 TACTTGAGAAGCTGAGGCAGGAGGACTGCTTGAAGCCAGGAGTTTGAGACCAGCCTGGGCAACAT TACTTGAGAAGCTGAGGCAGGAGGACTGCTTGCAGCCAGGAGTTTGAGACCAGCCTGGGCAACAT A C SPN,QPRT Ensembl:ENSG00000197471,Ensembl:ENSG00000103485 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells chr16:29669068..29669069 24183664 RNA-Seq:(High) rs12929333 Functional Loss SNV ICGC 33..33 33 LAML 1 - 53246 RMVar_ID_53246 Human_SNP_ID_827451620 A-to-I Human chr16 + 66890101 66890101 66890101 CAGGAGTTTGAGACCAGCCTGACCAACATGGTAAAACTCCATCTCTACTAAAAATACAAAAATTA CAGGAGTTTGAGACCAGCCTGACCAACATGGTGAAACTCCATCTCTACTAAAAATACAAAAATTA A G PDP2 Ensembl:ENSG00000172840 Protein coding 3'UTR GSE47997;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;Bronchiolar epithelium,BERP35T4 cell line chr16:66890100..66890101;chr16:66890101..66890102 23474544,31158229,31158229,31158229,31158229 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_90756,RMVar_hsa_circ_178998 53247 RMVar_ID_53247 Human_SNP_ID_827455348 A-to-I Human chr16 - 74489236 74489236 74489236 AAACTCTGGACCTCAGGTGATCTTCCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTAAG AAACTCTGGACCTCAGGTGATCTTCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTAAG T C GLG1 Ensembl:ENSG00000090863 Protein coding intron GSE38233 cultured B-cells chr16:74489235..74489236 24183664 RNA-Seq:(High) rs557470974 Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_2752,RMVar_hsa_circ_268623,RMVar_hsa_circ_371700,RMVar_hsa_circ_179941,RMVar_hsa_circ_45525,RMVar_hsa_circ_104398,RMVar_hsa_circ_179953,RMVar_hsa_circ_26037,RMVar_hsa_circ_15226,RMVar_hsa_circ_66790,RMVar_hsa_circ_355930,RMVar_hsa_circ_350256,RMVar_hsa_circ_67380,RMVar_hsa_circ_39089,RMVar_hsa_circ_358004,RMVar_hsa_circ_315293,RMVar_hsa_circ_358039,RMVar_hsa_circ_369361,RMVar_hsa_circ_108207,RMVar_hsa_circ_20644,RMVar_hsa_circ_291967,RMVar_hsa_circ_179962,RMVar_hsa_circ_179963,RMVar_hsa_circ_179961,RMVar_hsa_circ_342637,RMVar_hsa_circ_368884,RMVar_hsa_circ_336210 53248 RMVar_ID_53248 Human_SNP_ID_827457014 A-to-I Human chr16 + 19120113 19120113 19120113 GTTTTTGTTTTTGTTTTTTGAGACAGGGTCTCAGTCTGTTGCCCAGGCTGGAGTGCAGTGGCAAG GTTTTTGTTTTTGTTTTTTGAGACAGGGTCTCGGTCTGTTGCCCAGGCTGGAGTGCAGTGGCAAG A G ITPRIPL2,AC099518.3 Ensembl:ENSG00000205730,Ensembl:ENSG00000261427 Protein coding,lincRNA 3'UTR,exon GSE38233 cultured B-cells chr16:19120112..19120113 24183664 RNA-Seq:(High) rs57236534 Functional Loss SNV ICGC 33..33 33 LUSC 2 - Human_Splice_Rec_1685800 RMVar_hsa_circ_117690,RMVar_hsa_circ_82653,RMVar_hsa_circ_176897,RMVar_hsa_circ_176898 53249 RMVar_ID_53249 Human_SNP_ID_827488686 A-to-I Human chr16 + 89988293 89988293 89988293 CTCACTGCAGACTTGAACTCCCAGGCACAAGCAATCCTCTTACCTCAGCCTCCTGAGGAGCTGGA CTCACTGCAGACTTGAACTCCCAGGCACAAGCCATCCTCTTACCTCAGCCTCCTGAGGAGCTGGA A C AFG3L1P Ensembl:ENSG00000223959 Pseudogene intron GSE100210 HepG2 cell line chr16:89988292..89988293;chr16:89988293..89988294 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_5247328,Human_RBP_ID_9840750,Human_RBP_ID_17564506,Human_RBP_ID_18513260,Human_RBP_ID_23307819 RMVar_hsa_circ_70110,RMVar_hsa_circ_60878,RMVar_hsa_circ_353793,RMVar_hsa_circ_81285,RMVar_hsa_circ_180866 53250 RMVar_ID_53250 Human_SNP_ID_827493747 A-to-I Human chr16 + 76554690 76554690 76554690 TACACTCTGAATATGATACGGATATAGAAAGTAAACAATTATTCTGTTGCATTGCCAGGGAGATA TACACTCTGAATATGATACGGATATAGAAAGTTAACAATTATTCTGTTGCATTGCCAGGGAGATA A T AC106741.2,CNTNAP4 Ensembl:ENSG00000287694,Ensembl:ENSG00000152910 Protein coding,Protein coding intron,intron GSE47997;GSE100210;GSE100210;GSE107867 K562 cells&HepG2 cells;HepG2 cell line;HepG2 cell line;ASD brains,frontal_cortex chr16:76554689..76554690;chr16:76554690..76554691 23474544,29129909,29129909,30559470 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 13 pancreas RMVar_hsa_circ_180115 53251 RMVar_ID_53251 Human_SNP_ID_827520271 A-to-I Human chr16 - 4304810 4304810 4304810 CCACCCTAGCCTCCCGAGAAGCTGGGATCACAAGCGCCCACCACCACACCAAACTAATTTTGTAT CCACCCTAGCCTCCCGAGAAGCTGGGATCACACGCGCCCACCACCACACCAAACTAATTTTGTAT T G lnc-TFAP4-3,lnc-TFAP4-3:2,lnc-TFAP4-3:3,lnc-TFAP4-3:4,lnc-TFAP4-3:5 RNACentral:URS0000D574AE,RNACentral:URS0000D5E22E,RNACentral:URS00008BBD57,RNACentral:URS0000D5DCB2,RNACentral:URS0000D5D47B lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,exon,intron GSE100210 HepG2 cell line chr16:4304809..4304810 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 53252 RMVar_ID_53252 Human_SNP_ID_827520579 A-to-I Human chr16 + 623486 623485 623486 CCTGGCTAACACGGTGAAACCCTGTCTCTACTAAAAAAAAATACAAAAAAATTAGCCGGGCATGG CCTGGCTAACACGGTGAAACCCTGTCTCTACT_AAAAAAAATACAAAAAAATTAGCCGGGCATGG TA T RAB40C Ensembl:ENSG00000197562 Protein coding intron GSE47997 K562 cells&HepG2 cells chr16:623486..623487 23474544 RNA-Seq:(High) - Functional Loss DEL ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_25403,RMVar_hsa_circ_68144 53253 RMVar_ID_53253 Human_SNP_ID_827541704 A-to-I Human chr16 + 30491280 30491280 30491280 AAAATTAGCCAGGCATGGTGGCATGCACCTGTAATCCCAGCTACTCGGGAGGCTGAGGTAGGAGA AAAATTAGCCAGGCATGGTGGCATGCACCTGTGATCCCAGCTACTCGGGAGGCTGAGGTAGGAGA A G ITGAL Ensembl:ENSG00000005844 Protein coding intron GSE38233 cultured B-cells chr16:30491280..30491281 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_86007,RMVar_hsa_circ_98934,RMVar_hsa_circ_177881,RMVar_hsa_circ_369439,RMVar_hsa_circ_177882,RMVar_hsa_circ_17761,RMVar_hsa_circ_87381,RMVar_hsa_circ_107545,RMVar_hsa_circ_177883,RMVar_hsa_circ_177885,RMVar_hsa_circ_177888,RMVar_hsa_circ_59739,RMVar_hsa_circ_355696,RMVar_hsa_circ_18399,RMVar_hsa_circ_55760,RMVar_hsa_circ_81430,RMVar_hsa_circ_2195,RMVar_hsa_circ_177891,RMVar_hsa_circ_112392,RMVar_hsa_circ_101347,RMVar_hsa_circ_177892,RMVar_hsa_circ_177893 53254 RMVar_ID_53254 Human_SNP_ID_827568481 A-to-I Human chr16 + 89519602 89519602 89519602 TGGGGTTTCTGCATGTTGGTCAGGCTTGTCTCAGACTCCCGACCTCAGGTGATGCACCCGCCTCA TGGGGTTTCTGCATGTTGGTCAGGCTTGTCTCGGACTCCCGACCTCAGGTGATGCACCCGCCTCA A G SPG7 Ensembl:ENSG00000197912 Protein coding intron GSE38233 cultured B-cells chr16:89519601..89519602 24183664 RNA-Seq:(High) rs12050940 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_8442948,Human_RBP_ID_12855669 Clinvar_Rec_87,Clinvar_Rec_88 GWAS_ID_2174,GWAS_ID_2175,GWAS_ID_2176,GWAS_ID_2177,GWAS_ID_2178,GWAS_ID_2179,GWAS_ID_2180,GWAS_ID_2181,GWAS_ID_2182,GWAS_ID_2183,GWAS_ID_2184,GWAS_ID_2185,GWAS_ID_2186,GWAS_ID_2187,GWAS_ID_2188,GWAS_ID_2189,GWAS_ID_2190,GWAS_ID_2191,GWAS_ID_2192,GWAS_ID_2193,GWAS_ID_2194,GWAS_ID_2195,GWAS_ID_2196,GWAS_ID_2197,GWAS_ID_2198,GWAS_ID_2199,GWAS_ID_2200,GWAS_ID_2201,GWAS_ID_2202,GWAS_ID_2203,GWAS_ID_2204,GWAS_ID_2205,GWAS_ID_2206,GWAS_ID_2207,GWAS_ID_2208,GWAS_ID_2209,GWAS_ID_2210,GWAS_ID_2211,GWAS_ID_2212,GWAS_ID_2213,GWAS_ID_2214,GWAS_ID_2215,GWAS_ID_2216,GWAS_ID_2217,GWAS_ID_2218,GWAS_ID_2219,GWAS_ID_2220,GWAS_ID_2221,GWAS_ID_2222,GWAS_ID_2223,GWAS_ID_2224,GWAS_ID_2225,GWAS_ID_2226,GWAS_ID_2227,GWAS_ID_2228,GWAS_ID_2229,GWAS_ID_2230,GWAS_ID_2231,GWAS_ID_2232,GWAS_ID_2233 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 53255 RMVar_ID_53255 Human_SNP_ID_827570035 A-to-I Human chr16 + 1362862 1362862 1362862 TAAAGAACTCTCAAAGGAGATCAAAAGGCTGAAAGGTTTGCTCACCCAGCACGGCATCCCCTACA TAAAGAACTCTCAAAGGAGATCAAAAGGCTGACAGGTTTGCTCACCCAGCACGGCATCCCCTACA A C GNPTG Ensembl:ENSG00000090581 Protein coding CDS GSE100210 HepG2 cell line chr16:1362862..1362863 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 READ,rectum adenocarcinoma,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_468476,Human_RBP_ID_1838194,Human_RBP_ID_22196635 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 53256 RMVar_ID_53256 Human_SNP_ID_827571460 A-to-I Human chr16 - 19704528 19704528 19704528 GGAGTGTGGTGGCGTGATCTCGGCTCATTGTAACCTCTGCTTCCTGGGTTCAAGCGATTCTTGTG GGAGTGTGGTGGCGTGATCTCGGCTCATTGTAGCCTCTGCTTCCTGGGTTCAAGCGATTCTTGTG T C KNOP1 Ensembl:ENSG00000103550 Protein coding 3'UTR GSE100210 HepG2 cell line chr16:19704527..19704528 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 53257 RMVar_ID_53257 Human_SNP_ID_827574008 A-to-I Human chr16 + 69162394 69162394 69162394 GGTCAGAAGTTCAAAACCAGCCCGGCCAACATAGTGAGACCCCGTTTCTACTAAAAATACAAAAA GGTCAGAAGTTCAAAACCAGCCCGGCCAACATGGTGAGACCCCGTTTCTACTAAAAATACAAAAA A G UTP4 Ensembl:ENSG00000141076 Protein coding intron GSE38233 cultured B-cells chr16:69162393..69162394 24183664 RNA-Seq:(High) rs1029367574 Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_1476,RMVar_hsa_circ_38462,RMVar_hsa_circ_51333,RMVar_hsa_circ_111704,RMVar_hsa_circ_6404,RMVar_hsa_circ_179337,RMVar_hsa_circ_333271,RMVar_hsa_circ_78632,RMVar_hsa_circ_179342,RMVar_hsa_circ_87595,RMVar_hsa_circ_179349,RMVar_hsa_circ_120977,RMVar_hsa_circ_179353,RMVar_hsa_circ_179352,RMVar_hsa_circ_125580,RMVar_hsa_circ_314470,RMVar_hsa_circ_374973,RMVar_hsa_circ_377000,RMVar_hsa_circ_284171,RMVar_hsa_circ_17433,RMVar_hsa_circ_179355,RMVar_hsa_circ_179356,RMVar_hsa_circ_179357,RMVar_hsa_circ_179354,RMVar_hsa_circ_271008,RMVar_hsa_circ_300664,RMVar_hsa_circ_179360,RMVar_hsa_circ_179361,RMVar_hsa_circ_179359 53258 RMVar_ID_53258 Human_SNP_ID_827589696 A-to-I Human chr16 - 88719124 88719124 88719124 AAACCCCGGGCCGGGCACAGCGGCTCACCCCTATCATCCCAGCACTGTAAGAGACCCAGGAGGGA AAACCCCGGGCCGGGCACAGCGGCTCACCCCTGTCATCCCAGCACTGTAAGAGACCCAGGAGGGA T C PIEZO1 Ensembl:ENSG00000103335 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr16:88719123..88719124 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_5183054,Human_RBP_ID_26951750 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 53259 RMVar_ID_53259 Human_SNP_ID_827607838 A-to-I Human chr16 + 69139152 69139152 69139152 CACCATGCCCGGCTAGTTTTTGTGTTTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGG CACCATGCCCGGCTAGTTTTTGTGTTTTTAGTGGAGACGGGGTTTCACCATGTTGGCCAGGCTGG A G UTP4 Ensembl:ENSG00000141076 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr16:69139151..69139152 24183664,29129909 RNA-Seq:(High) rs1280886081 Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_34831,RMVar_hsa_circ_123142,RMVar_hsa_circ_296623,RMVar_hsa_circ_38462,RMVar_hsa_circ_179331,RMVar_hsa_circ_339130,RMVar_hsa_circ_346703,RMVar_hsa_circ_51333,RMVar_hsa_circ_279753,RMVar_hsa_circ_48822,RMVar_hsa_circ_111704,RMVar_hsa_circ_179333,RMVar_hsa_circ_179335,RMVar_hsa_circ_6404,RMVar_hsa_circ_179334,RMVar_hsa_circ_179332,RMVar_hsa_circ_179337,RMVar_hsa_circ_94727,RMVar_hsa_circ_179336 53260 RMVar_ID_53260 Human_SNP_ID_827680161 A-to-I Human chr16 + 72278345 72278345 72278345 AGGTACTTGGAGAAGTCAGGGGTGCTGGACACACTGACCAAGGTGTTGGTATGAAGAACCAGAGA AGGTACTTGGAGAAGTCAGGGGTGCTGGACACGCTGACCAAGGTGTTGGTATGAAGAACCAGAGA A G AC009075.2 Ensembl:ENSG00000261774 Pseudogene exon GSE100210 HepG2 cell line chr16:72278344..72278345 29129909 RNA-Seq:(High) rs1467811907 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_5573414 53261 RMVar_ID_53261 Human_SNP_ID_827690723 A-to-I Human chr16 + 29668329 29668329 29668329 CACCTGCCTCAGCCTCCCAAAATGCTGGGACTATAGGCATGAGCCACTGCACCCAGCCACTGCTT CACCTGCCTCAGCCTCCCAAAATGCTGGGACTGTAGGCATGAGCCACTGCACCCAGCCACTGCTT A G SPN,QPRT Ensembl:ENSG00000197471,Ensembl:ENSG00000103485 Protein coding,Protein coding 3'UTR,intron GSE38233 cultured B-cells chr16:29668328..29668329 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_17564641 53262 RMVar_ID_53262 Human_SNP_ID_827740572 A-to-I Human chr16 - 74328769 74328769 74328769 CTCAAAAAATAAATTAACAGATCAGGCGCAGTAGCTCACACCTGTAATCCCAGCACTTTGGGAGG CTCAAAAAATAAATTAACAGATCAGGCGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGG T C AC009120.2 Ensembl:ENSG00000259972 lincRNA intron GSE100210 HepG2 cell line chr16:74328768..74328769 29129909 RNA-Seq:(High) rs1348420478 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_5096769 53263 RMVar_ID_53263 Human_SNP_ID_827819240 A-to-I Human chr16 - 89787172 89787172 89787172 TTCCTGCCTCAACCTCCCAAAGTGTTGGAATTACCGGATTGAGCCACTGCACCCAGCCATTAAGT TTCCTGCCTCAACCTCCCAAAGTGTTGGAATTGCCGGATTGAGCCACTGCACCCAGCCATTAAGT T C FANCA Ensembl:ENSG00000187741 Protein coding intron GSE100210 HepG2 cell line chr16:89787171..89787172 29129909 RNA-Seq:(High) rs760767856 Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_12860045 RMVar_hsa_circ_180690,RMVar_hsa_circ_104573,RMVar_hsa_circ_118985,RMVar_hsa_circ_124924,RMVar_hsa_circ_104647,RMVar_hsa_circ_180692,RMVar_hsa_circ_180693,RMVar_hsa_circ_180691,RMVar_hsa_circ_29947,RMVar_hsa_circ_269291,RMVar_hsa_circ_107379,RMVar_hsa_circ_180702,RMVar_hsa_circ_36627,RMVar_hsa_circ_335628,RMVar_hsa_circ_114220,RMVar_hsa_circ_180715,RMVar_hsa_circ_180714,RMVar_hsa_circ_115747,RMVar_hsa_circ_119521,RMVar_hsa_circ_112173,RMVar_hsa_circ_180732,RMVar_hsa_circ_37285,RMVar_hsa_circ_57204,RMVar_hsa_circ_180733,RMVar_hsa_circ_180734,RMVar_hsa_circ_57797,RMVar_hsa_circ_84503,RMVar_hsa_circ_180735,RMVar_hsa_circ_110423,RMVar_hsa_circ_80022,RMVar_hsa_circ_89693,RMVar_hsa_circ_180739,RMVar_hsa_circ_180740,RMVar_hsa_circ_93729,RMVar_hsa_circ_100923,RMVar_hsa_circ_180742,RMVar_hsa_circ_180744,RMVar_hsa_circ_180743,RMVar_hsa_circ_104046,RMVar_hsa_circ_3101,RMVar_hsa_circ_95425,RMVar_hsa_circ_102907,RMVar_hsa_circ_180745,RMVar_hsa_circ_106799,RMVar_hsa_circ_180747,RMVar_hsa_circ_128184,RMVar_hsa_circ_180748,RMVar_hsa_circ_111171,RMVar_hsa_circ_94376,RMVar_hsa_circ_180752,RMVar_hsa_circ_180753,RMVar_hsa_circ_180754,RMVar_hsa_circ_180751,RMVar_hsa_circ_268508,RMVar_hsa_circ_45994 53264 RMVar_ID_53264 Human_SNP_ID_844830423 A-to-I Human chr3 - 75424931 75424931 75424931 TTGGCCAGGCTGATCTTGAACTCCTGACCTCAAGTGATCTGCTGTCTCAGCCTCCCAAAGTGTTA TTGGCCAGGCTGATCTTGAACTCCTGACCTCATGTGATCTGCTGTCTCAGCCTCCCAAAGTGTTA T A FAM86DP Ensembl:ENSG00000244026 Pseudogene intron GSE100210 HepG2 cell line chr3:75424930..75424931 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - 53265 RMVar_ID_53265 Human_SNP_ID_844865012 A-to-I Human chr3 - 197093299 197093299 197093299 CAAAAATTAGCTGGGCATGTTAGCGCATGTCTATAGTCCCAGCTCCTTGGGAGGCTGAAGCAGGA CAAAAATTAGCTGGGCATGTTAGCGCATGTCTGTAGTCCCAGCTCCTTGGGAGGCTGAAGCAGGA T C DLG1 Ensembl:ENSG00000075711 Protein coding intron GSE100210 HepG2 cell line chr3:197093298..197093299 29129909 RNA-Seq:(High) rs575717765 Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_5763,RMVar_hsa_circ_85652,RMVar_hsa_circ_297506,RMVar_hsa_circ_223981,RMVar_hsa_circ_223973,RMVar_hsa_circ_223974,RMVar_hsa_circ_310965,RMVar_hsa_circ_341386,RMVar_hsa_circ_223982,RMVar_hsa_circ_93038,RMVar_hsa_circ_3357,RMVar_hsa_circ_223984,RMVar_hsa_circ_333126,RMVar_hsa_circ_294112,RMVar_hsa_circ_376756,RMVar_hsa_circ_223985,RMVar_hsa_circ_326025,RMVar_hsa_circ_267147,RMVar_hsa_circ_53949,RMVar_hsa_circ_71965,RMVar_hsa_circ_223986,RMVar_hsa_circ_221,RMVar_hsa_circ_320592,RMVar_hsa_circ_290538,RMVar_hsa_circ_322818,RMVar_hsa_circ_273633,RMVar_hsa_circ_223989,RMVar_hsa_circ_29084,RMVar_hsa_circ_223990,RMVar_hsa_circ_286389,RMVar_hsa_circ_288731,RMVar_hsa_circ_279367,RMVar_hsa_circ_223996,RMVar_hsa_circ_53827,RMVar_hsa_circ_223992,RMVar_hsa_circ_223993,RMVar_hsa_circ_303869,RMVar_hsa_circ_341360,RMVar_hsa_circ_223991,RMVar_hsa_circ_311760,RMVar_hsa_circ_270761,RMVar_hsa_circ_24766,RMVar_hsa_circ_38198,RMVar_hsa_circ_223998,RMVar_hsa_circ_223999,RMVar_hsa_circ_223997 53266 RMVar_ID_53266 Human_SNP_ID_844917770 A-to-I Human chr3 - 106651311 106651311 106651311 TGAATCCGGGAGGCGGAGGTTGCTGTGGGCCGAGATCGCGCCACTGCACTCCAGCCTAGGCTACA TGAATCCGGGAGGCGGAGGTTGCTGTGGGCCGCGATCGCGCCACTGCACTCCAGCCTAGGCTACA T G LINC00882 Ensembl:ENSG00000242759 lincRNA intron GSE100210 HepG2 cell line chr3:106651310..106651311 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 2 - 53267 RMVar_ID_53267 Human_SNP_ID_844923883 A-to-I Human chr3 - 47917503 47917503 47917503 CGGTTCATTGCAAACTCCGCCTCCTGGGTTCTAGCAATTCTCCTGCTTCAGCCTCCCAAGTAGCT CGGTTCATTGCAAACTCCGCCTCCTGGGTTCTGGCAATTCTCCTGCTTCAGCCTCCCAAGTAGCT T C MAP4 Ensembl:ENSG00000047849 Protein coding intron GSE100210 HepG2 cell line chr3:47917502..47917503 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_217783,RMVar_hsa_circ_124585,RMVar_hsa_circ_81267,RMVar_hsa_circ_125095,RMVar_hsa_circ_217787,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_354131,RMVar_hsa_circ_376246,RMVar_hsa_circ_353045,RMVar_hsa_circ_282301,RMVar_hsa_circ_217798,RMVar_hsa_circ_217797,RMVar_hsa_circ_269105,RMVar_hsa_circ_331968 53268 RMVar_ID_53268 Human_SNP_ID_844957334 A-to-I Human chr3 + 100576961 100576961 100576961 GTTAAATCTAGACTTAAGAGGCTCTGCTCCTCAGAAGTTGGACTTCTGAAAAATGCTGAACGAGA GTTAAATCTAGACTTAAGAGGCTCTGCTCCTCGGAAGTTGGACTTCTGAAAAATGCTGAACGAGA A G TMEM45A Ensembl:ENSG00000181458 Protein coding CDS GSE100210 HepG2 cell line chr3:100576960..100576961 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 head_neck squamous_cell_carcinoma,skin squamous_cell_carcinoma 2 skin,head and neck Human_RBP_ID_583873 Human_Splice_Rec_459106,Human_Splice_Rec_459120,Human_Splice_Rec_459140,Human_Splice_Rec_459142 RMVar_hsa_circ_102492,RMVar_hsa_circ_88225,RMVar_hsa_circ_220018,RMVar_hsa_circ_103683,RMVar_hsa_circ_220021,RMVar_hsa_circ_220022 53269 RMVar_ID_53269 Human_SNP_ID_845061613 A-to-I Human chr3 - 186795710 186795710 186795710 CGGCTCACTGCAACCTCCACATCCCGGGTTCAAGCAATCCTCCTGCCTCAGCCTCCTGAGTAGCT CGGCTCACTGCAACCTCCACATCCCGGGTTCATGCAATCCTCCTGCCTCAGCCTCCTGAGTAGCT T A RFC4 Ensembl:ENSG00000163918 Protein coding intron GSE100210 HepG2 cell line chr3:186795709..186795710 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_58528,RMVar_hsa_circ_35076,RMVar_hsa_circ_223590,RMVar_hsa_circ_75940,RMVar_hsa_circ_274551,RMVar_hsa_circ_223593,RMVar_hsa_circ_335678,RMVar_hsa_circ_343037,RMVar_hsa_circ_372025,RMVar_hsa_circ_223594 53270 RMVar_ID_53270 Human_SNP_ID_845063788 A-to-I Human chr3 + 174006813 174006812 174006813 GATTAAGGCCAGGCATGGGGGCTCCTGCTTGTAACCCCAGCACTCTGGGAGGCCGAGGTAGGTGG GATTAAGGCCAGGCATGGGGGCTCCTGCTTGT_ACCCCAGCACTCTGGGAGGCCGAGGTAGGTGG TA T NLGN1 Ensembl:ENSG00000169760 Protein coding intron GSE107867 ASD brains,cerebellum chr3:174006813..174006814 30559470 RNA-Seq:(High) - Functional Loss DEL ICGC 33..33 33 CLLE 1 - 53271 RMVar_ID_53271 Human_SNP_ID_845084152 A-to-I Human chr3 - 113730095 113730095 113730095 GGGTTTCACCATGTTGGCCAGGCCAGTGTTGAACTCCTGGCTTCAAGTGATCCACCCGAGTCAGC GGGTTTCACCATGTTGGCCAGGCCAGTGTTGATCTCCTGGCTTCAAGTGATCCACCCGAGTCAGC T A NAA50 Ensembl:ENSG00000121579 Protein coding intron GSE100210 HepG2 cell line chr3:113730094..113730095 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_14568726 53272 RMVar_ID_53272 Human_SNP_ID_845130609 A-to-I Human chr3 + 11431604 11431604 11431604 CCCTGGCAACCACTAATCTTCTTTCTGTCTGTAAGGATTTTTCTATTCTGGACACATCACATAAA CCCTGGCAACCACTAATCTTCTTTCTGTCTGTGAGGATTTTTCTATTCTGGACACATCACATAAA A G ATG7 Ensembl:ENSG00000197548 Protein coding intron GSE100210 HepG2 cell line chr3:11431604..11431605 29129909 RNA-Seq:(High) rs758760177 Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_108562,RMVar_hsa_circ_215894,RMVar_hsa_circ_215904 53273 RMVar_ID_53273 Human_SNP_ID_845281888 A-to-I Human chr3 + 39409101 39409101 39409101 GCCGAGACTCTGTCTCAAAAAAAAAAAAAAAGAAAATAGAAAACTCAAACTCCACTGTTAAGAGA GCCGAGACTCTGTCTCAAAAAAAAAAAAAAAGGAAATAGAAAACTCAAACTCCACTGTTAAGAGA A G RPSA Ensembl:ENSG00000168028 Protein coding intron GSE47997 K562 cells&HepG2 cells chr3:39409100..39409101 23474544 RNA-Seq:(High) rs79217109 Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 6 prostate 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 53274 RMVar_ID_53274 Human_SNP_ID_845290052 A-to-I Human chr3 + 50098649 50098649 50098649 TATTTTTAGTAGAGACGGGATTTCACTGTGTTAGCCAGGATGGTCTCCATCTCTTGACCTCGTGA TATTTTTAGTAGAGACGGGATTTCACTGTGTTGGCCAGGATGGTCTCCATCTCTTGACCTCGTGA A G RBM5,RBM6 Ensembl:ENSG00000003756,Ensembl:ENSG00000004534 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells chr3:50098648..50098649 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 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_96641,RMVar_hsa_circ_218343,RMVar_hsa_circ_6084,RMVar_hsa_circ_218342,RMVar_hsa_circ_109449,RMVar_hsa_circ_93262,RMVar_hsa_circ_218348,RMVar_hsa_circ_54594,RMVar_hsa_circ_275888,RMVar_hsa_circ_218344,RMVar_hsa_circ_218345,RMVar_hsa_circ_218346,RMVar_hsa_circ_365390,RMVar_hsa_circ_285567,RMVar_hsa_circ_92660,RMVar_hsa_circ_114763,RMVar_hsa_circ_66297,RMVar_hsa_circ_218350,RMVar_hsa_circ_218351,RMVar_hsa_circ_218352,RMVar_hsa_circ_218349 53275 RMVar_ID_53275 Human_SNP_ID_845310830 A-to-I Human chr3 - 133631012 133631012 133631012 GCTAATTGTATTTTTTGGAGAGGTAGAGTCTCACCATGTTGCTCAGGCTGGTCTAGAACTCCTGG GCTAATTGTATTTTTTGGAGAGGTAGAGTCTCTCCATGTTGCTCAGGCTGGTCTAGAACTCCTGG T A TOPBP1 Ensembl:ENSG00000163781 Protein coding intron GSE100210 HepG2 cell line chr3:133631011..133631012 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 3 pancreas RMVar_hsa_circ_327111,RMVar_hsa_circ_347661,RMVar_hsa_circ_221408,RMVar_hsa_circ_126215,RMVar_hsa_circ_221409,RMVar_hsa_circ_266588,RMVar_hsa_circ_356538,RMVar_hsa_circ_345819,RMVar_hsa_circ_94542,RMVar_hsa_circ_121394,RMVar_hsa_circ_221415,RMVar_hsa_circ_269426,RMVar_hsa_circ_221417,RMVar_hsa_circ_111387,RMVar_hsa_circ_221416,RMVar_hsa_circ_75241,RMVar_hsa_circ_41386,RMVar_hsa_circ_221419,RMVar_hsa_circ_311132,RMVar_hsa_circ_321879,RMVar_hsa_circ_335217,RMVar_hsa_circ_310118,RMVar_hsa_circ_69525,RMVar_hsa_circ_221421,RMVar_hsa_circ_221422,RMVar_hsa_circ_221423,RMVar_hsa_circ_221425,RMVar_hsa_circ_48297,RMVar_hsa_circ_299471,RMVar_hsa_circ_325767,RMVar_hsa_circ_307155,RMVar_hsa_circ_57080,RMVar_hsa_circ_221424 53276 RMVar_ID_53276 Human_SNP_ID_845315484 A-to-I Human chr3 + 135925970 135925970 135925970 AGAGACAAATATCTGGGGCCTGCAGTTCTTATACAGGCCTATCACTGGATGATTGACTCCAGAGA AGAGACAAATATCTGGGGCCTGCAGTTCTTATGCAGGCCTATCACTGGATGATTGACTCCAGAGA A G AC092989.1 Ensembl:ENSG00000242222 Pseudogene exon GSE100210 HepG2 cell line chr3:135925969..135925970 29129909 RNA-Seq:(High) rs576055885 Functional Loss SNV ICGC 33..33 33 LAML 1 - 53277 RMVar_ID_53277 Human_SNP_ID_845329867 A-to-I Human chr3 - 56674503 56674501 56674503 AGCATTTTATTTTTTATTTTTATTTTTGAGACAGGGTCTCTCTCTCACTCCCAGACTGGAGTGCG AGCATTTTATTTTTTATTTTTATTTTTGAGAC__GGTCTCTCTCTCACTCCCAGACTGGAGTGCG CCT C TASOR Ensembl:ENSG00000163946 Protein coding intron GSE38233 cultured B-cells chr3:56674502..56674503 24183664 RNA-Seq:(High) rs1256133913 Functional Loss DEL ICGC 33..34 33 PBCA 1 - Human_RBP_ID_26685871 RMVar_hsa_circ_120967,RMVar_hsa_circ_219059 53278 RMVar_ID_53278 Human_SNP_ID_845370286 A-to-I Human chr3 + 184138862 184138862 184138862 TTTGTATTTTTTTGTAGAGACGGGGTTTTGCCATGTTGTCCGGCCTGGTCACGAACTCCTGAGCT TTTGTATTTTTTTGTAGAGACGGGGTTTTGCCGTGTTGTCCGGCCTGGTCACGAACTCCTGAGCT A G EIF2B5 Ensembl:ENSG00000145191 Protein coding intron GSE100210 HepG2 cell line chr3:184138861..184138862 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_Splice_Rec_514946,Human_Splice_Rec_514976,Human_Splice_Rec_515034 RMVar_hsa_circ_223287,RMVar_hsa_circ_73420,RMVar_hsa_circ_375025 53279 RMVar_ID_53279 Human_SNP_ID_845404884 A-to-I Human chr3 - 49087691 49087691 49087691 TTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTTGAACTCCTGACCT TTTTGTATTTTTAGTAGAGATGGGGTTTCACCGTGTTGGCCAGGCTGGTCTTGAACTCCTGACCT T C QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE38233 cultured B-cells chr3:49087690..49087691 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_10931 53280 RMVar_ID_53280 Human_SNP_ID_845447371 A-to-I Human chr3 - 14944928 14944928 14944928 TGGCTCATGCCTGTAATCCCAGCATTTTGGGAAGGTGAGGTGGGTGGATCACCTGAGGTCAGGAG TGGCTCATGCCTGTAATCCCAGCATTTTGGGAGGGTGAGGTGGGTGGATCACCTGAGGTCAGGAG T C FGD5-AS1 Ensembl:ENSG00000225733 lincRNA intron GSE38233 cultured B-cells chr3:14944927..14944928 24183664 RNA-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 53281 RMVar_ID_53281 Human_SNP_ID_845451101 A-to-I Human chr3 - 49393570 49393570 49393570 AAAAAAAGCCAGTGCAGTGGCCTACACCTGTAATCTGAGCACTTTGGGAGGCCAAGGCAGGTAGA AAAAAAAGCCAGTGCAGTGGCCTACACCTGTAGTCTGAGCACTTTGGGAGGCCAAGGCAGGTAGA T C RHOA Ensembl:ENSG00000067560 Protein coding intron GSE38233 cultured B-cells chr3:49393569..49393570 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 4 oesophagus RMVar_hsa_circ_91759,RMVar_hsa_circ_126650,RMVar_hsa_circ_218167,RMVar_hsa_circ_218168,RMVar_hsa_circ_218172,RMVar_hsa_circ_124898,RMVar_hsa_circ_82726,RMVar_hsa_circ_218171 53282 RMVar_ID_53282 Human_SNP_ID_845477137 A-to-I Human chr3 - 48699939 48699939 48699939 GCAATCTTCCCATCTTGGCCTCCCAAAGTGCTAGGATTACAAGGAGTGAGCCACTGTACCCAGCC GCAATCTTCCCATCTTGGCCTCCCAAAGTGCTGGGATTACAAGGAGTGAGCCACTGTACCCAGCC T C IP6K2 Ensembl:ENSG00000068745 Protein coding intron GSE38233 cultured B-cells chr3:48699938..48699939 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_14859040 RMVar_hsa_circ_82807,RMVar_hsa_circ_217975 53283 RMVar_ID_53283 Human_SNP_ID_845526762 A-to-I Human chr3 - 50335829 50335829 50335829 GGCCAAGGCAGGTGGATCATTTGCAATCAGGAATTCGAGGTCAGCCTGGCCAACATGGTGAAACC GGCCAAGGCAGGTGGATCATTTGCAATCAGGAGTTCGAGGTCAGCCTGGCCAACATGGTGAAACC T C RASSF1 Ensembl:ENSG00000068028 Protein coding intron GSE38233 cultured B-cells chr3:50335828..50335829 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 6 liver Human_RBP_ID_2789903,Human_RBP_ID_14877677 53284 RMVar_ID_53284 Human_SNP_ID_845539831 A-to-I Human chr3 + 42092820 42092820 42092820 ATTGCCCAGGCTGGTTTTGAATTCCTGGGCTCAAGTGATCCCCCTGCCTCGGCCTCCCAAAGTGC ATTGCCCAGGCTGGTTTTGAATTCCTGGGCTCGAGTGATCCCCCTGCCTCGGCCTCCCAAAGTGC A G TRAK1 Ensembl:ENSG00000182606 Protein coding intron GSE100210 HepG2 cell line chr3:42092820..42092821 29129909 RNA-Seq:(High) rs1464735100 Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_56960,RMVar_hsa_circ_289985,RMVar_hsa_circ_69649,RMVar_hsa_circ_77431,RMVar_hsa_circ_217215,RMVar_hsa_circ_217216 53285 RMVar_ID_53285 Human_SNP_ID_845578098 A-to-I Human chr3 - 51972324 51972324 51972324 CTCAGGTGATCCGCCCGCCTCGGCCTCCCAAAATGCTGGGATTACAGGCGTGTGCCACCGCGCCT CTCAGGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGTGCCACCGCGCCT T C PCBP4,ABHD14B,AC115284.1 Ensembl:ENSG00000090097,Ensembl:ENSG00000114779,Ensembl:ENSG00000272762 Protein coding,Protein coding,lincRNA intron,intron,intron GSE47997 K562 cells&HepG2 cells chr3:51972323..51972324 23474544 RNA-Seq:(High) rs1339891221 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 15 liver 53286 RMVar_ID_53286 Human_SNP_ID_845608594 A-to-I Human chr3 + 9995676 9995676 9995676 TTCTGTTTTTTGAGACGGAGTCTAGCTCTGTCACCTAGACTGGAGTGCAGTTGGCGCTGTCTCAG TTCTGTTTTTTGAGACGGAGTCTAGCTCTGTCTCCTAGACTGGAGTGCAGTTGGCGCTGTCTCAG A T EMC3-AS1 Ensembl:ENSG00000180385 Pseudogene intron GSE100210 HepG2 cell line chr3:9995675..9995676 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_248006,Human_RBP_ID_14544729,Human_RBP_ID_17990041,Human_RBP_ID_18536136 RMVar_hsa_circ_107386,RMVar_hsa_circ_215751 53287 RMVar_ID_53287 Human_SNP_ID_845693972 A-to-I Human chr3 - 179398280 179398280 179398280 GTACTCCTGGCCTCAAGTGATCCACCAGCCTCAGCCTCCCAAAGTGCTGGGATTACAGACGTGAG GTACTCCTGGCCTCAAGTGATCCACCAGCCTCGGCCTCCCAAAGTGCTGGGATTACAGACGTGAG T C GNB4 Ensembl:ENSG00000114450 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line chr3:179398279..179398280 29129909,31158229 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 2 breast RMVar_hsa_circ_105486,RMVar_hsa_circ_117926,RMVar_hsa_circ_128128,RMVar_hsa_circ_110542,RMVar_hsa_circ_222912,RMVar_hsa_circ_89333,RMVar_hsa_circ_94368,RMVar_hsa_circ_222914,RMVar_hsa_circ_85129,RMVar_hsa_circ_222915,RMVar_hsa_circ_222913,RMVar_hsa_circ_222910,RMVar_hsa_circ_222911,RMVar_hsa_circ_222909 53288 RMVar_ID_53288 Human_SNP_ID_845753303 A-to-I Human chr3 - 101576880 101576880 101576880 TTTGCGAGTACTCAACACCAACATCGATGGGCAGCGGAAAATAGCCTTTGCCATCACTGCCATTA TTTGCGAGTACTCAACACCAACATCGATGGGCGGCGGAAAATAGCCTTTGCCATCACTGCCATTA T C AC073861.1 Ensembl:ENSG00000242299 Pseudogene exon GSE107867 ASD brains,cerebellum chr3:101576879..101576880 30559470 RNA-Seq:(High) rs879170249 Functional Loss SNV ICGC,COSMIC 33..33 33 breast ductal_carcinoma,STAD 5 breast Human_RBP_ID_584090 53289 RMVar_ID_53289 Human_SNP_ID_845768688 A-to-I Human chr3 + 141896406 141896406 141896406 AGCTGGGCACGGTGGTATGTGCCTGTAGTCCTAGCTACTGGGGAGGCTGGGGCAGGAGGATTGCT AGCTGGGCACGGTGGTATGTGCCTGTAGTCCTCGCTACTGGGGAGGCTGGGGCAGGAGGATTGCT A C ATP1B3 Ensembl:ENSG00000069849 Protein coding intron GSE100210 HepG2 cell line chr3:141896405..141896406 29129909 RNA-Seq:(High) rs1171484439 Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_8560619,Human_RBP_ID_23973867 53290 RMVar_ID_53290 Human_SNP_ID_845808626 A-to-I Human chr3 + 111913374 111913374 111913374 CCTCAGTCTCTGTGCTGAATACACAAAGCCTGACAGTCGCTTATCTACTGGGACCACCGTGGAAG CCTCAGTCTCTGTGCTGAATACACAAAGCCTGTCAGTCGCTTATCTACTGGGACCACCGTGGAAG A T PHLDB2 Ensembl:ENSG00000144824 Protein coding CDS GSE100210 HepG2 cell line chr3:111913373..111913374 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 9 lung Human_RBP_ID_67790,Human_RBP_ID_5601803,Human_RBP_ID_9393915 Human_Splice_Rec_466514,Human_Splice_Rec_466546,Human_Splice_Rec_466578,Human_Splice_Rec_466612,Human_Splice_Rec_466642,Human_Splice_Rec_466646,Human_Splice_Rec_466678,Human_Splice_Rec_466708,Human_Splice_Rec_466728 RMVar_hsa_circ_220261,RMVar_hsa_circ_45973,RMVar_hsa_circ_58960,RMVar_hsa_circ_66165,RMVar_hsa_circ_376745,RMVar_hsa_circ_48416,RMVar_hsa_circ_113502,RMVar_hsa_circ_121506,RMVar_hsa_circ_220262,RMVar_hsa_circ_220264,RMVar_hsa_circ_220268,RMVar_hsa_circ_337064,RMVar_hsa_circ_350116,RMVar_hsa_circ_354119,RMVar_hsa_circ_359240,RMVar_hsa_circ_352759,RMVar_hsa_circ_347627,RMVar_hsa_circ_281349,RMVar_hsa_circ_298849,RMVar_hsa_circ_118216,RMVar_hsa_circ_220266,RMVar_hsa_circ_220267,RMVar_hsa_circ_220265,RMVar_hsa_circ_220263 53291 RMVar_ID_53291 Human_SNP_ID_845808636 A-to-I Human chr3 + 111913374 111913374 111913374 CCTCAGTCTCTGTGCTGAATACACAAAGCCTGACAGTCGCTTATCTACTGGGACCACCGTGGAAG CCTCAGTCTCTGTGCTGAATACACAAAGCCTGCCAGTCGCTTATCTACTGGGACCACCGTGGAAG A C PHLDB2 Ensembl:ENSG00000144824 Protein coding CDS GSE100210 HepG2 cell line chr3:111913373..111913374 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 7 brain Human_RBP_ID_67790,Human_RBP_ID_5601803,Human_RBP_ID_9393915 Human_Splice_Rec_466514,Human_Splice_Rec_466546,Human_Splice_Rec_466578,Human_Splice_Rec_466612,Human_Splice_Rec_466642,Human_Splice_Rec_466646,Human_Splice_Rec_466678,Human_Splice_Rec_466708,Human_Splice_Rec_466728 RMVar_hsa_circ_220261,RMVar_hsa_circ_45973,RMVar_hsa_circ_58960,RMVar_hsa_circ_66165,RMVar_hsa_circ_376745,RMVar_hsa_circ_48416,RMVar_hsa_circ_113502,RMVar_hsa_circ_121506,RMVar_hsa_circ_220262,RMVar_hsa_circ_220264,RMVar_hsa_circ_220268,RMVar_hsa_circ_337064,RMVar_hsa_circ_350116,RMVar_hsa_circ_354119,RMVar_hsa_circ_359240,RMVar_hsa_circ_352759,RMVar_hsa_circ_347627,RMVar_hsa_circ_281349,RMVar_hsa_circ_298849,RMVar_hsa_circ_118216,RMVar_hsa_circ_220266,RMVar_hsa_circ_220267,RMVar_hsa_circ_220265,RMVar_hsa_circ_220263 53292 RMVar_ID_53292 Human_SNP_ID_845826427 A-to-I Human chr3 - 47777430 47777430 47777430 CCTCGTCCTCCCAAAGTACTGGGATTACAGTCATGAGCCACTGCACCCGGCCTATATTCACTGTA CCTCGTCCTCCCAAAGTACTGGGATTACAGTCGTGAGCCACTGCACCCGGCCTATATTCACTGTA T C SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233 cultured B-cells chr3:47777429..47777430 24183664 RNA-Seq:(High) rs917945765 Functional Loss SNV ICGC 33..33 33 MALY 1 - 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 53293 RMVar_ID_53293 Human_SNP_ID_845882629 A-to-I Human chr3 - 136690410 136690410 136690410 CAACATGGTGAAACCTCATCTCTACTAAAAATACAAAAATTAGTTGGGCATGGTGGCGTGGGCCT CAACATGGTGAAACCTCATCTCTACTAAAAATTCAAAAATTAGTTGGGCATGGTGGCGTGGGCCT T A STAG1 Ensembl:ENSG00000118007 Protein coding intron GSE100210 HepG2 cell line chr3:136690409..136690410 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 STAD 1 - RMVar_hsa_circ_47258 53294 RMVar_ID_53294 Human_SNP_ID_845884235 A-to-I Human chr3 - 179593872 179593872 179593872 TCTTTTCAGGTAGTAGATTCCATGGATGCATTAGATAAAGTTGTCCAGGAAAGAGAAGATGCCCT TCTTTTCAGGTAGTAGATTCCATGGATGCATTGGATAAAGTTGTCCAGGAAAGAGAAGATGCCCT T C MRPL47 Ensembl:ENSG00000136522 Protein coding CDS GSE100210 HepG2 cell line chr3:179593871..179593872 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 5 head and neck Human_RBP_ID_595682,Human_RBP_ID_1622822,Human_RBP_ID_9136463,Human_RBP_ID_14737292,Human_RBP_ID_23986984,Human_RBP_ID_26825081 Human_Splice_Rec_509408,Human_Splice_Rec_509420,Human_Splice_Rec_509430 Human_miRNA_ID_2508751 RMVar_hsa_circ_80097,RMVar_hsa_circ_222934,RMVar_hsa_circ_222937,RMVar_hsa_circ_222939,RMVar_hsa_circ_271328,RMVar_hsa_circ_272904,RMVar_hsa_circ_300090,RMVar_hsa_circ_126809,RMVar_hsa_circ_222938,RMVar_hsa_circ_222936 53295 RMVar_ID_53295 Human_SNP_ID_845933374 A-to-I Human chr3 - 129168430 129168430 129168430 ACCACACCCAGCTAATTTTTGTTATTTTTAGTAGAGATGGGGTTTCACTGTGTTGGTCAGGCTGG ACCACACCCAGCTAATTTTTGTTATTTTTAGTTGAGATGGGGTTTCACTGTGTTGGTCAGGCTGG T A CNBP Ensembl:ENSG00000169714 Protein coding 3'UTR GSE38233 cultured B-cells chr3:129168429..129168430 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_76874,RMVar_hsa_circ_221109 53296 RMVar_ID_53296 Human_SNP_ID_845933380 A-to-I Human chr3 - 129168430 129168430 129168430 ACCACACCCAGCTAATTTTTGTTATTTTTAGTAGAGATGGGGTTTCACTGTGTTGGTCAGGCTGG ACCACACCCAGCTAATTTTTGTTATTTTTAGTGGAGATGGGGTTTCACTGTGTTGGTCAGGCTGG T C CNBP Ensembl:ENSG00000169714 Protein coding 3'UTR GSE38233 cultured B-cells chr3:129168429..129168430 24183664 RNA-Seq:(High) rs1317171582 Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_76874,RMVar_hsa_circ_221109 53297 RMVar_ID_53297 Human_SNP_ID_845995213 A-to-I Human chr3 - 170462662 170462662 170462662 CAGTGGCATGATCTTGGCTCACTGCAACCTTCACCTCCCGGGTTCAAGCTATTCTCCTGCCTCAG CAGTGGCATGATCTTGGCTCACTGCAACCTTCCCCTCCCGGGTTCAAGCTATTCTCCTGCCTCAG T G SLC7A14 Ensembl:ENSG00000013293 Protein coding 3'UTR GSE107867 ASD brains,temporal_cortex chr3:170462661..170462662 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 53298 RMVar_ID_53298 Human_SNP_ID_846033533 A-to-I Human chr3 + 52690448 52690448 52690448 CCACGCCCAGCTAATTTTTTTGTATTTTTAGTAGAGACGGGGTTTTATCGTGTTAGCCAGGATGG CCACGCCCAGCTAATTTTTTTGTATTTTTAGTGGAGACGGGGTTTTATCGTGTTAGCCAGGATGG A G GNL3 Ensembl:ENSG00000163938 Protein coding intron GSE47997 K562 cells&HepG2 cells chr3:52690447..52690448 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - RMVar_hsa_circ_8685,RMVar_hsa_circ_124111,RMVar_hsa_circ_71418,RMVar_hsa_circ_63351,RMVar_hsa_circ_17945,RMVar_hsa_circ_348884,RMVar_hsa_circ_218769,RMVar_hsa_circ_363275,RMVar_hsa_circ_307136,RMVar_hsa_circ_61085,RMVar_hsa_circ_218770,RMVar_hsa_circ_371874,RMVar_hsa_circ_218772 53299 RMVar_ID_53299 Human_SNP_ID_846077476 A-to-I Human chr3 - 65959943 65959943 65959943 AAATTAGCTGGGCGTGATGGCGGGCTCCTGTAATCACAGCTACTCTGGAGGCTGAGGCAGGAGAA AAATTAGCTGGGCGTGATGGCGGGCTCCTGTAGTCACAGCTACTCTGGAGGCTGAGGCAGGAGAA T C MAGI1 Ensembl:ENSG00000151276 Protein coding intron GSE47997 K562 cells&HepG2 cells chr3:65959942..65959943 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_106022,RMVar_hsa_circ_219443,RMVar_hsa_circ_87074,RMVar_hsa_circ_219454 53300 RMVar_ID_53300 Human_SNP_ID_846099296 A-to-I Human chr3 - 155849783 155849783 155849783 CTGCCTCAGCCTCCCTAGTAGCTGGGATTATAAGCGTGTGCCACCATGCCTGGCTAATTTTTGTA CTGCCTCAGCCTCCCTAGTAGCTGGGATTATAGGCGTGTGCCACCATGCCTGGCTAATTTTTGTA T C SLC33A1,AC104472.3 Ensembl:ENSG00000169359,Ensembl:ENSG00000284952 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells chr3:155849782..155849783 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 5 haematopoietic and lymphoid tissue 53301 RMVar_ID_53301 Human_SNP_ID_846183159 A-to-I Human chr3 + 122614915 122614915 122614915 AGCCGGGCGTGGTGGTGTACATCTGTAGTCCCAGCTACTTGGGAGGCTGAGGTGGGAGGATCAGT AGCCGGGCGTGGTGGTGTACATCTGTAGTCCCTGCTACTTGGGAGGCTGAGGTGGGAGGATCAGT A T PARP15 Ensembl:ENSG00000173200 Protein coding intron GSE38233 cultured B-cells chr3:122614914..122614915 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 3 liver RMVar_hsa_circ_71462,RMVar_hsa_circ_356477,RMVar_hsa_circ_362185,RMVar_hsa_circ_220667 53302 RMVar_ID_53302 Human_SNP_ID_846190980 A-to-I Human chr3 - 196062489 196062489 196062489 TGCTCTTGTCGCCCAGGCTGGAGTGCAATGGCACGATCTCGGCTCACTGCAACCTCTGTCTCCCA TGCTCTTGTCGCCCAGGCTGGAGTGCAATGGCGCGATCTCGGCTCACTGCAACCTCTGTCTCCCA T C TFRC Ensembl:ENSG00000072274 Protein coding intron GSE100210 HepG2 cell line chr3:196062488..196062489 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue RMVar_hsa_circ_67433,RMVar_hsa_circ_223845,RMVar_hsa_circ_111324,RMVar_hsa_circ_121595,RMVar_hsa_circ_128066,RMVar_hsa_circ_80284,RMVar_hsa_circ_223846,RMVar_hsa_circ_223843,RMVar_hsa_circ_223844,RMVar_hsa_circ_340292,RMVar_hsa_circ_363377,RMVar_hsa_circ_334288,RMVar_hsa_circ_308948,RMVar_hsa_circ_3131,RMVar_hsa_circ_22311,RMVar_hsa_circ_223854,RMVar_hsa_circ_65137,RMVar_hsa_circ_223853,RMVar_hsa_circ_377340,RMVar_hsa_circ_103045,RMVar_hsa_circ_340924,RMVar_hsa_circ_223855,RMVar_hsa_circ_223856,RMVar_hsa_circ_343677,RMVar_hsa_circ_367866,RMVar_hsa_circ_341777,RMVar_hsa_circ_310545,RMVar_hsa_circ_321932,RMVar_hsa_circ_59092,RMVar_hsa_circ_106356,RMVar_hsa_circ_34129,RMVar_hsa_circ_103477,RMVar_hsa_circ_223857,RMVar_hsa_circ_223859,RMVar_hsa_circ_223860,RMVar_hsa_circ_223858,RMVar_hsa_circ_223863,RMVar_hsa_circ_126589,RMVar_hsa_circ_370056,RMVar_hsa_circ_370440,RMVar_hsa_circ_223865,RMVar_hsa_circ_21161,RMVar_hsa_circ_223866,RMVar_hsa_circ_223864 53303 RMVar_ID_53303 Human_SNP_ID_846207630 A-to-I Human chr3 + 128071406 128071406 128071406 CAGAGGGGCAGGGCCTCCCCCAGCCCACGCTTAGGAATGCTTGGCCTCTGGCAGGCAGGCAGCTG CAGAGGGGCAGGGCCTCCCCCAGCCCACGCTTGGGAATGCTTGGCCTCTGGCAGGCAGGCAGCTG A G SEC61A1 Ensembl:ENSG00000058262 Protein coding 3'UTR GSE38233 cultured B-cells chr3:128071405..128071406 24183664 RNA-Seq:(High) rs1042995 Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_588523,Human_RBP_ID_1617133,Human_RBP_ID_7117360,Human_RBP_ID_8557836,Human_RBP_ID_17702753,Human_RBP_ID_27497742 Human_miRNA_ID_1190222,Human_miRNA_ID_1952892 RMVar_hsa_circ_85911,RMVar_hsa_circ_221030,RMVar_hsa_circ_87757,RMVar_hsa_circ_109992,RMVar_hsa_circ_221034,RMVar_hsa_circ_221036,RMVar_hsa_circ_96417,RMVar_hsa_circ_221037,RMVar_hsa_circ_221038,RMVar_hsa_circ_99254 53304 RMVar_ID_53304 Human_SNP_ID_846230843 A-to-I Human chr3 - 130108266 130108256 130108266 AACCCAGCACAAGGCTGGGTGCACTGGTTCACACCTGTAATCCCAGGACATTGGGAGGCTGAGGT AACCCAGCACAAGGCTGGGTGCACTGGTTCAC__________CCAGGACATTGGGAGGCTGAGGT GGATTACAGGT G FAM86HP Ensembl:ENSG00000253540 Pseudogene intron GSE100210 HepG2 cell line chr3:130108265..130108266 29129909 RNA-Seq:(High) rs1360422560 Functional Loss DEL ICGC 33..42 33 PBCA 1 - Human_RBP_ID_17406204 53305 RMVar_ID_53305 Human_SNP_ID_846245977 A-to-I Human chr3 - 47498261 47498261 47498261 ACGGGCAGGTATGCAGGGGCCTCCTGGGCAACAGGCTTCTTGCCCGTGTACCTGTGATTCTTGAC ACGGGCAGGTATGCAGGGGCCTCCTGGGCAACGGGCTTCTTGCCCGTGTACCTGTGATTCTTGAC T C ELP6 Ensembl:ENSG00000163832 Protein coding intron GSE38233 cultured B-cells chr3:47498260..47498261 24183664 RNA-Seq:(High) rs2170814 Functional Loss SNV ICGC 33..33 33 COCA 5 - Human_RBP_ID_835517,Human_RBP_ID_933080,Human_RBP_ID_19115329 RMVar_hsa_circ_118529,RMVar_hsa_circ_128056,RMVar_hsa_circ_217622,RMVar_hsa_circ_111628,RMVar_hsa_circ_217623,RMVar_hsa_circ_217621 53306 RMVar_ID_53306 Human_SNP_ID_846252193 A-to-I Human chr3 + 12539189 12539189 12539189 GTAGTCTCGCTCTGTCGTCCAGGCTGGAGTCCAATGCTGCGATCTTGGATCACTGCAACCTCTGC GTAGTCTCGCTCTGTCGTCCAGGCTGGAGTCCGATGCTGCGATCTTGGATCACTGCAACCTCTGC A G TSEN2 Ensembl:ENSG00000154743 Protein coding exon GSE38233 cultured B-cells chr3:12539189..12539190 24183664 RNA-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 53307 RMVar_ID_53307 Human_SNP_ID_846265446 A-to-I Human chr3 - 10018193 10018193 10018193 CAGGGTTTTACCATGTTGGCCACACTGGTCTCAAACTCCTGACCTCAGGTGACTCACCCACCACG CAGGGTTTTACCATGTTGGCCACACTGGTCTCTAACTCCTGACCTCAGGTGACTCACCCACCACG T A CIDECP1 Ensembl:ENSG00000186162 Pseudogene intron GSE38233 cultured B-cells chr3:10018192..10018193 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_17405333 RMVar_hsa_circ_215750 53308 RMVar_ID_53308 Human_SNP_ID_846269370 A-to-I Human chr3 - 17872499 17872499 17872499 ATGAGAAAGGACAATATATATCTCCATTTCATAATATTCCAATTTATGCAGATAAGGATGTGTTC ATGAGAAAGGACAATATATATCTCCATTTCATGATATTCCAATTTATGCAGATAAGGATGTGTTC T C TBC1D5,AC104297.1 Ensembl:ENSG00000131374,Ensembl:ENSG00000213383 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line chr3:17872498..17872499 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_miRNA_ID_1901877 53309 RMVar_ID_53309 Human_SNP_ID_846300771 A-to-I Human chr3 - 94059249 94059249 94059249 TGATTTTGCCACTGCACTCCTGCCTGGGTGACAGAAGAGACCCTGTCTCAAAAAAGAATCTGAAA TGATTTTGCCACTGCACTCCTGCCTGGGTGACGGAAGAGACCCTGTCTCAAAAAAGAATCTGAAA T C DHFR2 Ensembl:ENSG00000178700 Protein coding intron GSE100210 HepG2 cell line chr3:94059248..94059249 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 RECA 1 - 53310 RMVar_ID_53310 Human_SNP_ID_846345954 A-to-I Human chr3 - 121833226 121833226 121833226 GATATAAGAAGGCAGCCAGCAAAGATGGTCTTAAAATGTAGTATGATGGTAGAACTGGGCTTTAA GATATAAGAAGGCAGCCAGCAAAGATGGTCTTTAAATGTAGTATGATGGTAGAACTGGGCTTTAA T A IQCB1 Ensembl:ENSG00000173226 Protein coding intron GSE100210;GSE99789;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line chr3:121833225..121833226 29129909,29796672,32596459,32596459 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_7111220 53311 RMVar_ID_53311 Human_SNP_ID_846384071 A-to-I Human chr3 - 49081981 49081981 49081981 CAACACGGTGATACCCTGTCTCTACTAAAAATACAAAAATTAGCTGGGCATGGTGGCGTATGCCT CAACACGGTGATACCCTGTCTCTACTAAAAATGCAAAAATTAGCTGGGCATGGTGGCGTATGCCT T C QRICH1 Ensembl:ENSG00000198218 Protein coding intron GSE38233 cultured B-cells chr3:49081980..49081981 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_10931 53312 RMVar_ID_53312 Human_SNP_ID_846414986 A-to-I Human chr3 + 44371109 44371109 44371109 AATTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTGGCTAGACTGGTCTCGAACTCTTGA AATTTTTGTATTTTTAGTAGAGACGGGGTTTCGCCATGTTGGCTAGACTGGTCTCGAACTCTTGA A G TCAIM Ensembl:ENSG00000179152 Protein coding intron GSE100210 HepG2 cell line chr3:44371108..44371109 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_27656,RMVar_hsa_circ_296563,RMVar_hsa_circ_362091,RMVar_hsa_circ_303038,RMVar_hsa_circ_217304,RMVar_hsa_circ_217305,RMVar_hsa_circ_313964,RMVar_hsa_circ_217306,RMVar_hsa_circ_217313,RMVar_hsa_circ_285136,RMVar_hsa_circ_340669,RMVar_hsa_circ_363312,RMVar_hsa_circ_217312,RMVar_hsa_circ_273610,RMVar_hsa_circ_217311,RMVar_hsa_circ_217315,RMVar_hsa_circ_294452,RMVar_hsa_circ_341370,RMVar_hsa_circ_292534,RMVar_hsa_circ_217314,RMVar_hsa_circ_217317,RMVar_hsa_circ_282096,RMVar_hsa_circ_298646,RMVar_hsa_circ_64084,RMVar_hsa_circ_217316 53313 RMVar_ID_53313 Human_SNP_ID_846418693 A-to-I Human chr3 - 96350548 96350548 96350548 ATCAGCACTGAAACCAACCATGCCATGGTAACAGTCTCCAGGTCTCCCTCTTCTGTCATAGGCCA ATCAGCACTGAAACCAACCATGCCATGGTAACGGTCTCCAGGTCTCCCTCTTCTGTCATAGGCCA T C lnc-MTRNR2L12-9 RNACentral:URS00009BA044 lincRNA exon GSE100210 HepG2 cell line chr3:96350547..96350548 29129909 RNA-Seq:(High) rs878860346 Functional Loss SNV ICGC 33..33 33 LAML 2 - 53314 RMVar_ID_53314 Human_SNP_ID_846433169 A-to-I Human chr3 + 47186768 47186768 47186768 CCTGTAATCCCAGCACTTTAGGAGGCCAAGGCAGGTGGACAACTTGAGGCCAGGAGTTGGAGACC CCTGTAATCCCAGCACTTTAGGAGGCCAAGGCGGGTGGACAACTTGAGGCCAGGAGTTGGAGACC A G KIF9-AS1 Ensembl:ENSG00000227398 lincRNA intron GSE100210 HepG2 cell line chr3:47186767..47186768 29129909 RNA-Seq:(High) rs1343560235 Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_82426,RMVar_hsa_circ_217555 53315 RMVar_ID_53315 Human_SNP_ID_846442988 A-to-I Human chr3 + 39333556 39333556 39333556 GCCAACACTTGGAACACAATGACTAAAGACATAGTTGTGCATGCCTGGCACAACATCAAGCCTGT GCCAACACTTGGAACACAATGACTAAAGACATGGTTGTGCATGCCTGGCACAACATCAAGCCTGT A G CCR8 Ensembl:ENSG00000179934 Protein coding 3'UTR GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells chr3:39333555..39333556 23474544,24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - 53316 RMVar_ID_53316 Human_SNP_ID_846469044 A-to-I Human chr3 - 183087663 183087663 183087663 GGGGTTTCACTGTGTTAGCCAGGACGGTCTCAATCTCCTGACCTCATGATCCGCCCGCCTTGGCC GGGGTTTCACTGTGTTAGCCAGGACGGTCTCAGTCTCCTGACCTCATGATCCGCCCGCCTTGGCC T C MCCC1 Ensembl:ENSG00000078070 Protein coding intron GSE47997 K562 cells&HepG2 cells chr3:183087662..183087663 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 9 breast RMVar_hsa_circ_223092,RMVar_hsa_circ_365888,RMVar_hsa_circ_223096,RMVar_hsa_circ_293363,RMVar_hsa_circ_333240,RMVar_hsa_circ_223095,RMVar_hsa_circ_265759,RMVar_hsa_circ_223097,RMVar_hsa_circ_31448,RMVar_hsa_circ_276935,RMVar_hsa_circ_293717,RMVar_hsa_circ_223098 53317 RMVar_ID_53317 Human_SNP_ID_846479915 A-to-I Human chr3 + 37276114 37276114 37276114 TCCTCGGGCACCAAGCACTTCTGATTCTGTGCAGTTGAAGTGTAGGGAGATGCTTGCTGCAGCTC TCCTCGGGCACCAAGCACTTCTGATTCTGTGCGGTTGAAGTGTAGGGAGATGCTTGCTGCAGCTC A G TCEA1P2,GOLGA4 Ensembl:ENSG00000230409,Ensembl:ENSG00000144674 Pseudogene,Protein coding exon,intron GSE107867 ASD brains,frontal_cortex chr3:37276113..37276114 30559470 RNA-Seq:(High) rs1380853105 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 5 haematopoietic and lymphoid tissue Human_RBP_ID_1205263,Human_RBP_ID_3723325,Human_RBP_ID_17195308,Human_RBP_ID_26346599,Human_RBP_ID_27823074 RMVar_hsa_circ_1723,RMVar_hsa_circ_61622,RMVar_hsa_circ_77830,RMVar_hsa_circ_216999,RMVar_hsa_circ_353326,RMVar_hsa_circ_301231,RMVar_hsa_circ_62266,RMVar_hsa_circ_38378,RMVar_hsa_circ_52092,RMVar_hsa_circ_12711,RMVar_hsa_circ_265050,RMVar_hsa_circ_278608,RMVar_hsa_circ_306619,RMVar_hsa_circ_352827,RMVar_hsa_circ_217001,RMVar_hsa_circ_321372,RMVar_hsa_circ_283510,RMVar_hsa_circ_269453,RMVar_hsa_circ_63008,RMVar_hsa_circ_75162,RMVar_hsa_circ_50216,RMVar_hsa_circ_217003,RMVar_hsa_circ_217004,RMVar_hsa_circ_217005,RMVar_hsa_circ_217002 53318 RMVar_ID_53318 Human_SNP_ID_846512680 A-to-I Human chr3 - 44578326 44578326 44578326 CTTGCACAGGGCAAGGATGCCTATGAACTAGAAGTCTTATTGCGGATATAGGAATCGGAAATACA CTTGCACAGGGCAAGGATGCCTATGAACTAGAGGTCTTATTGCGGATATAGGAATCGGAAATACA T C ZKSCAN7-AS1 Ensembl:ENSG00000236869 lincRNA intron GSE100210 HepG2 cell line chr3:44578325..44578326 29129909 RNA-Seq:(High) rs1310036647 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 haematopoietic and lymphoid tissue Human_RBP_ID_5604385 53319 RMVar_ID_53319 Human_SNP_ID_846516303 A-to-I Human chr3 - 44578248 44578248 44578248 GAGATTAGCTCCCTCAAGGATGAGCTGCAGACAGCACTGTGGGACAAGAAGTACGCAAGTGACAC GAGATTAGCTCCCTCAAGGATGAGCTGCAGACGGCACTGTGGGACAAGAAGTACGCAAGTGACAC T C ZKSCAN7-AS1 Ensembl:ENSG00000236869 lincRNA intron GSE38233 cultured B-cells chr3:44578247..44578248 24183664 RNA-Seq:(High) rs1191983101 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue Human_RBP_ID_5602442 53320 RMVar_ID_53320 Human_SNP_ID_846581108 A-to-I Human chr3 - 65439928 65439928 65439928 AAGAAGCAGCTTGAGCAGCAGCAGCAGCAGCAACAGCAGCAGCAACAGCAGCAGCAGCAGCAGCA AAGAAGCAGCTTGAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAACAGCAGCAGCAGCAGCAGCA T C MAGI1 Ensembl:ENSG00000151276 Protein coding CDS GSE56152 embryonic stem cells,wild type chr3:65439927..65439928 25708366 RNA-Seq:(High) rs62642828 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,COCA,stomach diffuse_adenocarcinoma,large_intestine adenocarcinoma 20 caecum,stomach,large intestine Human_RBP_ID_27822350 Human_Splice_Rec_449678,Human_Splice_Rec_449679,Human_Splice_Rec_449724,Human_Splice_Rec_449725,Human_Splice_Rec_449766,Human_Splice_Rec_449767,Human_Splice_Rec_449814,Human_Splice_Rec_449815,Human_Splice_Rec_449856,Human_Splice_Rec_449857,Human_Splice_Rec_449900,Human_Splice_Rec_449901,Human_Splice_Rec_449940,Human_Splice_Rec_449941,Human_Splice_Rec_449984,Human_Splice_Rec_449985,Human_Splice_Rec_450018,Human_Splice_Rec_450019,Human_Splice_Rec_450082,Human_Splice_Rec_450083,Human_Splice_Rec_450092,Human_Splice_Rec_450093,Human_Splice_Rec_450104,Human_Splice_Rec_450105 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_350792,RMVar_hsa_circ_350841,RMVar_hsa_circ_293269,RMVar_hsa_circ_106022,RMVar_hsa_circ_49996,RMVar_hsa_circ_828,RMVar_hsa_circ_22726,RMVar_hsa_circ_104085,RMVar_hsa_circ_267821,RMVar_hsa_circ_219443,RMVar_hsa_circ_341062,RMVar_hsa_circ_301204,RMVar_hsa_circ_379058,RMVar_hsa_circ_283860,RMVar_hsa_circ_319383,RMVar_hsa_circ_337395,RMVar_hsa_circ_351980,RMVar_hsa_circ_288827,RMVar_hsa_circ_219445,RMVar_hsa_circ_219447,RMVar_hsa_circ_70633,RMVar_hsa_circ_219448,RMVar_hsa_circ_219446,RMVar_hsa_circ_294304,RMVar_hsa_circ_326893,RMVar_hsa_circ_347980,RMVar_hsa_circ_61252,RMVar_hsa_circ_283863,RMVar_hsa_circ_54272,RMVar_hsa_circ_219450,RMVar_hsa_circ_219452,RMVar_hsa_circ_219453,RMVar_hsa_circ_219451 53321 RMVar_ID_53321 Human_SNP_ID_846584494 A-to-I Human chr3 + 4545548 4545546 4545548 AGGAGGCTGAGGTGTAAGGATCTCTGGACCCTAGGAGACTGAAGCTGAAGTGAGCCATGACTGTG AGGAGGCTGAGGTGTAAGGATCTCTGGACCC__GGAGACTGAAGCTGAAGTGAGCCATGACTGTG CTA C ITPR1 Ensembl:ENSG00000150995 Protein coding intron GSE100210 HepG2 cell line chr3:4545547..4545548 29129909 RNA-Seq:(High) rs1324704800 Functional Loss DEL ICGC 32..33 33 PBCA 1 - 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 53322 RMVar_ID_53322 Human_SNP_ID_846614592 A-to-I Human chr3 + 128065835 128065835 128065835 CTCGACTCGACTCACTGCAACCTCCGCCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCG CTCGACTCGACTCACTGCAACCTCCGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCG A G SEC61A1 Ensembl:ENSG00000058262 Protein coding intron GSE100210 HepG2 cell line chr3:128065834..128065835 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 5 oesophagus Human_RBP_ID_14607760 RMVar_hsa_circ_121564,RMVar_hsa_circ_12871,RMVar_hsa_circ_85911,RMVar_hsa_circ_221029,RMVar_hsa_circ_20434,RMVar_hsa_circ_221030,RMVar_hsa_circ_377074,RMVar_hsa_circ_87757,RMVar_hsa_circ_221034 53323 RMVar_ID_53323 Human_SNP_ID_846623348 A-to-I Human chr3 - 27486518 27486518 27486518 CAAGCATAGCACTTGCGGCAGATCATCTTGTCACAGTTGTATTTCTGGGAGAGCTGGCAGAGGGA CAAGCATAGCACTTGCGGCAGATCATCTTGTCGCAGTTGTATTTCTGGGAGAGCTGGCAGAGGGA T C - - Other Unknown GSE100210 HepG2 cell line chr3:27486517..27486518 29129909 RNA-Seq:(High) rs878981397 Functional Loss SNV ICGC 33..33 33 LAML 1 - 53324 RMVar_ID_53324 Human_SNP_ID_846797119 A-to-I Human chr3 - 154284659 154284659 154284659 GGCTATGTCTGCTATTTTTAAGGGAAAAGAAAAGATTGCAGATGCAAGAAGAAAGGAATTGGCAA GGCTATGTCTGCTATTTTTAAGGGAAAAGAAACGATTGCAGATGCAAGAAGAAAGGAATTGGCAA T G DHX36 Ensembl:ENSG00000174953 Protein coding CDS GSE100210 HepG2 cell line chr3:154284658..154284659 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 5 stomach Human_RBP_ID_282467,Human_RBP_ID_1953057,Human_RBP_ID_3964306,Human_RBP_ID_23978600 Human_Splice_Rec_497386,Human_Splice_Rec_497387,Human_Splice_Rec_497484,Human_Splice_Rec_497485,Human_Splice_Rec_497500,Human_Splice_Rec_497501,Human_Splice_Rec_497542,Human_Splice_Rec_497543,Human_Splice_Rec_497564 RMVar_hsa_circ_45294,RMVar_hsa_circ_103393,RMVar_hsa_circ_222231,RMVar_hsa_circ_60815,RMVar_hsa_circ_32214,RMVar_hsa_circ_112228,RMVar_hsa_circ_222232,RMVar_hsa_circ_222234,RMVar_hsa_circ_222233,RMVar_hsa_circ_44876,RMVar_hsa_circ_222238,RMVar_hsa_circ_286689,RMVar_hsa_circ_23455,RMVar_hsa_circ_51817,RMVar_hsa_circ_330036,RMVar_hsa_circ_222239,RMVar_hsa_circ_337366,RMVar_hsa_circ_300280,RMVar_hsa_circ_125134,RMVar_hsa_circ_271215,RMVar_hsa_circ_72662,RMVar_hsa_circ_222240,RMVar_hsa_circ_222242,RMVar_hsa_circ_222244,RMVar_hsa_circ_222245,RMVar_hsa_circ_222246,RMVar_hsa_circ_222243,RMVar_hsa_circ_222241 53325 RMVar_ID_53325 Human_SNP_ID_846823672 A-to-I Human chr3 + 184149917 184149917 184149917 AGAAGGGCTGACGGATTCGGGAACTGACTGCTATAGTTCAGAAGAGGTTTGGCTTTCCAGAGGGC AGAAGGGCTGACGGATTCGGGAACTGACTGCTGTAGTTCAGAAGAGGTTTGGCTTTCCAGAGGGC A G AC131235.2 Ensembl:ENSG00000228205 Pseudogene exon GSE100210 HepG2 cell line chr3:184149916..184149917 29129909 RNA-Seq:(High) rs879049998 Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_596384,Human_RBP_ID_1064071,Human_RBP_ID_1957355,Human_RBP_ID_2770747,Human_RBP_ID_5602230,Human_RBP_ID_7167503,Human_RBP_ID_8566924,Human_RBP_ID_9137056,Human_RBP_ID_10113394,Human_RBP_ID_26505968 Human_miRNA_ID_1898764 53326 RMVar_ID_53326 Human_SNP_ID_846843592 A-to-I Human chr3 + 194589234 194589234 194589234 GTTGCCCAGGCTGATCTCGAACTCCTGGACCTAAGCAGTCCTCCCGCCTCAGCCTCCCAAAGTGC GTTGCCCAGGCTGATCTCGAACTCCTGGACCTCAGCAGTCCTCCCGCCTCAGCCTCCCAAAGTGC A C TMEM44-AS1 Ensembl:ENSG00000231770 lincRNA intron GSE100210 HepG2 cell line chr3:194589234..194589235 29129909 RNA-Seq:(High) rs12490914 Functional Loss SNV ICGC 33..33 33 ESCA 1 - 53327 RMVar_ID_53327 Human_SNP_ID_846877604 A-to-I Human chr3 - 119536479 119536479 119536479 AAAATTAGCCAGGCTTGGTGACACACATGTGTAGTCCTAGGTACTTGGGAGGGTAAGGTGGGTGG AAAATTAGCCAGGCTTGGTGACACACATGTGTGGTCCTAGGTACTTGGGAGGGTAAGGTGGGTGG T C CD80 Ensembl:ENSG00000121594 Protein coding intron GSE38233 cultured B-cells chr3:119536478..119536479 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 53328 RMVar_ID_53328 Human_SNP_ID_846878924 A-to-I Human chr3 - 47779196 47779196 47779196 ACAGGGTCTTTCTGTGTTGCCCAGGCTGGAGTACAGTGGCGTGATCATAGCTCACTGCAACCTCA ACAGGGTCTTTCTGTGTTGCCCAGGCTGGAGTGCAGTGGCGTGATCATAGCTCACTGCAACCTCA T C SMARCC1 Ensembl:ENSG00000173473 Protein coding intron GSE38233 cultured B-cells chr3:47779195..47779196 24183664 RNA-Seq:(High) rs1257667222 Functional Loss SNV ICGC 33..33 33 PRAD 3 - 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 53329 RMVar_ID_53329 Human_SNP_ID_846912367 A-to-I Human chr3 - 136713500 136713500 136713500 CGGCTCAGTGCAACTTCCACCTCCCGGATTCAAGCGATTCTTCTGCCTCAGCCTCCCGAGTAGCT CGGCTCAGTGCAACTTCCACCTCCCGGATTCACGCGATTCTTCTGCCTCAGCCTCCCGAGTAGCT T G STAG1 Ensembl:ENSG00000118007 Protein coding intron GSE100210 HepG2 cell line chr3:136713499..136713500 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 6 ovary Human_RBP_ID_14638380 RMVar_hsa_circ_47258 53330 RMVar_ID_53330 Human_SNP_ID_846961752 A-to-I Human chr3 - 53866662 53866653 53866663 CCTGGCTAACAGGGTGAAACCCCGTCTCTACTAAAAATATAAAAAGTTAGCTGGGTGTGGTGGTG CCTGGCTAACAGGGTGAAACCCCGTCTCTAC__________AAAAGTTAGCTGGGTGTGGTGGTG TTATATTTTTA T - - Other Unknown GSE100210 HepG2 cell line chr3:53866661..53866662 29129909 RNA-Seq:(High) rs77479324 Functional Loss DEL ICGC 32..41 33 LMS 1 - 53331 RMVar_ID_53331 Human_SNP_ID_846971699 A-to-I Human chr3 - 48162328 48162328 48162328 TGAGCCATGATCATGCCACTGTACTCCAGCCTAGGTGACAGAGTGAGATTCTGTCTCTCTCTCAC TGAGCCATGATCATGCCACTGTACTCCAGCCTTGGTGACAGAGTGAGATTCTGTCTCTCTCTCAC T A CDC25A Ensembl:ENSG00000164045 Protein coding intron GSE38233 cultured B-cells chr3:48162327..48162328 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 3 pancreas RMVar_hsa_circ_48846,RMVar_hsa_circ_118086,RMVar_hsa_circ_217814 53332 RMVar_ID_53332 Human_SNP_ID_847002635 A-to-I Human chr3 - 142845892 142845869 142845893 CGGCCCACTGCAACCTCCACCTCCCAGGTTCAAGCGATTTTTGTGCCTCAACCTCTCAAGCAGCT CGGCCCACTGCAACCTCCACCTCCCAGGTTC________________________TCAAGCAGCT AGAGGTTGAGGCACAAAAATCGCTT A PCOLCE2 Ensembl:ENSG00000163710 Protein coding intron GSE100210 HepG2 cell line chr3:142845891..142845892 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 32..55 33 BRCA 1 - RMVar_hsa_circ_222032,RMVar_hsa_circ_373571,RMVar_hsa_circ_72859,RMVar_hsa_circ_355778 53333 RMVar_ID_53333 Human_SNP_ID_847072414 A-to-I Human chr3 - 44750062 44750062 44750062 CACCCAGGCCAGACACAATGGCTCATGCTTGTAATCCCAACACTTTGGGAAGCCAAGGTGGGAGA CACCCAGGCCAGACACAATGGCTCATGCTTGTGATCCCAACACTTTGGGAAGCCAAGGTGGGAGA T C KIAA1143 Ensembl:ENSG00000163807 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line chr3:44750061..44750062 31158229 RNA-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 53334 RMVar_ID_53334 Human_SNP_ID_847093930 A-to-I Human chr3 - 180773598 180773598 180773598 TTAGAAGACTTGATTGTAATTTTGATATAAAGATTTTAAATGCACAGAGAGCAGAATACAAAGCA TTAGAAGACTTGATTGTAATTTTGATATAAAGGTTTTAAATGCACAGAGAGCAGAATACAAAGCA T C CCDC39,AC108734.3,AC108734.4 Ensembl:ENSG00000145075,Ensembl:ENSG00000242068,Ensembl:ENSG00000285336 lincRNA,Pseudogene,lincRNA intron,exon,intron GSE100210 HepG2 cell line chr3:180773597..180773598 29129909 RNA-Seq:(High) rs1023212705 Functional Loss SNV ICGC 33..33 33 LAML 1 - 53335 RMVar_ID_53335 Human_SNP_ID_847192701 A-to-I Human chr3 - 133628190 133628190 133628190 ATTTACCACATCTGTTGAAAATAGCCTCTCACATATCAATTCACTCTTATATGTATATAATGTAT ATTTACCACATCTGTTGAAAATAGCCTCTCACGTATCAATTCACTCTTATATGTATATAATGTAT T C TOPBP1 Ensembl:ENSG00000163781 Protein coding intron GSE38233 cultured B-cells chr3:133628189..133628190 24183664 RNA-Seq:(High) rs1550742 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_25697442 GWAS_ID_4785,GWAS_ID_4786,GWAS_ID_4787,GWAS_ID_4788,GWAS_ID_4789,GWAS_ID_4790,GWAS_ID_4791,GWAS_ID_4792,GWAS_ID_4793,GWAS_ID_4794,GWAS_ID_4795,GWAS_ID_4796,GWAS_ID_4797,GWAS_ID_4798,GWAS_ID_4799,GWAS_ID_4800,GWAS_ID_4801,GWAS_ID_4802,GWAS_ID_4803,GWAS_ID_4804 RMVar_hsa_circ_327111,RMVar_hsa_circ_347661,RMVar_hsa_circ_355820,RMVar_hsa_circ_221408,RMVar_hsa_circ_126215,RMVar_hsa_circ_221409,RMVar_hsa_circ_266588,RMVar_hsa_circ_356538,RMVar_hsa_circ_345819,RMVar_hsa_circ_50715,RMVar_hsa_circ_94542,RMVar_hsa_circ_90780,RMVar_hsa_circ_121394,RMVar_hsa_circ_221415,RMVar_hsa_circ_269426,RMVar_hsa_circ_221417,RMVar_hsa_circ_111387,RMVar_hsa_circ_221416,RMVar_hsa_circ_71684,RMVar_hsa_circ_75241,RMVar_hsa_circ_41386,RMVar_hsa_circ_221418,RMVar_hsa_circ_221419,RMVar_hsa_circ_311132,RMVar_hsa_circ_321879,RMVar_hsa_circ_335217,RMVar_hsa_circ_310118,RMVar_hsa_circ_69525,RMVar_hsa_circ_300581,RMVar_hsa_circ_45292,RMVar_hsa_circ_221421,RMVar_hsa_circ_221422,RMVar_hsa_circ_221423,RMVar_hsa_circ_265522,RMVar_hsa_circ_7745,RMVar_hsa_circ_48297 53336 RMVar_ID_53336 Human_SNP_ID_847232280 A-to-I Human chr3 - 15412545 15412545 15412545 AGAAGATGGAGGCTGCAGTGAGCTATGATCATACCACTGCCCTCCAGCCTGGGCGACAGGGCGAG AGAAGATGGAGGCTGCAGTGAGCTATGATCATGCCACTGCCCTCCAGCCTGGGCGACAGGGCGAG T C METTL6 Ensembl:ENSG00000206562 Protein coding intron GSE38233 cultured B-cells chr3:15412544..15412545 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - RMVar_hsa_circ_274004,RMVar_hsa_circ_271125,RMVar_hsa_circ_216172,RMVar_hsa_circ_216173 53337 RMVar_ID_53337 Human_SNP_ID_847279267 A-to-I Human chr3 + 160412606 160412606 160412606 TTGTGTGACTGAATGTGTTAGCTCATGCCTGTAATTCCAGCACTTTGGGAGGCTAAGGCAGGAGG TTGTGTGACTGAATGTGTTAGCTCATGCCTGTCATTCCAGCACTTTGGGAGGCTAAGGCAGGAGG A C SMC4 Ensembl:ENSG00000113810 Protein coding exon GSE38233 cultured B-cells chr3:160412605..160412606;chr3:160412606..160412607 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 5 oesophagus Human_RBP_ID_17622661,Human_RBP_ID_18801123,Human_RBP_ID_23981372 Human_Splice_Rec_501738,Human_Splice_Rec_501766 RMVar_hsa_circ_4254,RMVar_hsa_circ_31710,RMVar_hsa_circ_62770,RMVar_hsa_circ_18861,RMVar_hsa_circ_331574,RMVar_hsa_circ_14555,RMVar_hsa_circ_357246,RMVar_hsa_circ_357820,RMVar_hsa_circ_349415,RMVar_hsa_circ_373315,RMVar_hsa_circ_222426,RMVar_hsa_circ_333471,RMVar_hsa_circ_73889,RMVar_hsa_circ_279627,RMVar_hsa_circ_65042,RMVar_hsa_circ_63566,RMVar_hsa_circ_222427,RMVar_hsa_circ_222428,RMVar_hsa_circ_222429,RMVar_hsa_circ_67271,RMVar_hsa_circ_359771 53338 RMVar_ID_53338 Human_SNP_ID_847326005 A-to-I Human chr3 - 18538932 18538932 18538932 TGCTGGCAGGAGCTGACTGCTGAGTTGTAGCTAGTGCTGGTGTGGACACTGCTTTGGGTTCGGTC TGCTGGCAGGAGCTGACTGCTGAGTTGTAGCTGGTGCTGGTGTGGACACTGCTTTGGGTTCGGTC T C - - Other Unknown GSE107867 ASD brains,frontal_cortex chr3:18538931..18538932 30559470 RNA-Seq:(High) rs779219867 Functional Loss SNV ICGC 33..33 33 LAML 2 - 53339 RMVar_ID_53339 Human_SNP_ID_847349700 A-to-I Human chr3 - 195176195 195176195 195176195 GAAATTAGCGGGGCATGGTGGTACACACCTGTAGTCCCAGCCACTTGGGAGGCTGAGGTGGGAGG GAAATTAGCGGGGCATGGTGGTACACACCTGTGGTCCCAGCCACTTGGGAGGCTGAGGTGGGAGG T C XXYLT1 Ensembl:ENSG00000173950 Protein coding intron GSE100210 HepG2 cell line chr3:195176194..195176195 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_101781,RMVar_hsa_circ_117942,RMVar_hsa_circ_104920,RMVar_hsa_circ_223762,RMVar_hsa_circ_223764,RMVar_hsa_circ_223763,RMVar_hsa_circ_271065,RMVar_hsa_circ_13539,RMVar_hsa_circ_223767 53340 RMVar_ID_53340 Human_SNP_ID_847351617 A-to-I Human chr3 + 45533225 45533225 45533225 CAGGCTGGAGTGCAGTGGCGCGATCTCGGCTCACTGCAAGCTCCGCCTCCCGGGTTCACACCATT CAGGCTGGAGTGCAGTGGCGCGATCTCGGCTCGCTGCAAGCTCCGCCTCCCGGGTTCACACCATT A G LARS2 Ensembl:ENSG00000011376 Protein coding intron GSE100210 HepG2 cell line chr3:45533224..45533225 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 OV 1 - Human_RBP_ID_14831958 RMVar_hsa_circ_124359,RMVar_hsa_circ_89849,RMVar_hsa_circ_217402,RMVar_hsa_circ_217403,RMVar_hsa_circ_81698,RMVar_hsa_circ_217410,RMVar_hsa_circ_217417,RMVar_hsa_circ_117023,RMVar_hsa_circ_102986,RMVar_hsa_circ_217426,RMVar_hsa_circ_80218,RMVar_hsa_circ_217427 53341 RMVar_ID_53341 Human_SNP_ID_847425365 A-to-I Human chr3 + 40466116 40466091 40466117 GGGAGGCTGAGGCGGGAGAATCGCTTGAACCCAGGAGGTGGAGGTTGCAGTGAGCTGACATTACG GGGAGGCT__________________________GAGGTGGAGGTTGCAGTGAGCTGACATTACG TGAGGCGGGAGAATCGCTTGAACCCAG T RPL14 Ensembl:ENSG00000188846 Protein coding 3'UTR GSE100210 HepG2 cell line chr3:40466115..40466116 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 9..34 33 MELA 1 - 53342 RMVar_ID_53342 Human_SNP_ID_847443193 A-to-I Human chr3 - 100225548 100225548 100225548 TGCATAACGTAGCTCCTCCTCCATCTCTGCCAACGTTTCATTTGCTTCCTGTTGCTTTTCATCAA TGCATAACGTAGCTCCTCCTCCATCTCTGCCAGCGTTTCATTTGCTTCCTGTTGCTTTTCATCAA T C AC129803.1 Ensembl:ENSG00000287378 lincRNA intron GSE100210 HepG2 cell line chr3:100225547..100225548 29129909 RNA-Seq:(High) rs566185983 Functional Loss SNV ICGC 33..33 33 LAML 2 - 53343 RMVar_ID_53343 Human_SNP_ID_847479103 A-to-I Human chr3 - 122457730 122457730 122457730 GGCGTACCTCAACCTGGAGTGGGAAACTTGATAGGAGGTCAGAAGTACTTCAGCTTTGGATTCTC GGCGTACCTCAACCTGGAGTGGGAAACTTGATGGGAGGTCAGAAGTACTTCAGCTTTGGATTCTC T C KPNA1 Ensembl:ENSG00000114030 Protein coding intron GSE107867 ASD brains,temporal_cortex chr3:122457729..122457730 30559470 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_14589349,Human_RBP_ID_27711046 Human_Splice_Rec_473465,Human_Splice_Rec_473487,Human_Splice_Rec_473513,Human_Splice_Rec_473541 RMVar_hsa_circ_1926,RMVar_hsa_circ_343784,RMVar_hsa_circ_358978,RMVar_hsa_circ_114079,RMVar_hsa_circ_220655,RMVar_hsa_circ_313593,RMVar_hsa_circ_220657,RMVar_hsa_circ_42916,RMVar_hsa_circ_220656,RMVar_hsa_circ_70006,RMVar_hsa_circ_309531,RMVar_hsa_circ_325129,RMVar_hsa_circ_378476,RMVar_hsa_circ_220658,RMVar_hsa_circ_281420 53344 RMVar_ID_53344 Human_SNP_ID_847511636 A-to-I Human chr3 + 42584530 42584530 42584530 TGCCCGCCTTGGCCTCCCTAAGTGCTGGGATTACAGGCGTGAGCCACCACGCCTAGCCGGGACAT TGCCCGCCTTGGCCTCCCTAAGTGCTGGGATTGCAGGCGTGAGCCACCACGCCTAGCCGGGACAT A G SS18L2 Ensembl:ENSG00000008324 Protein coding intron GSE100210 HepG2 cell line chr3:42584529..42584530 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 53345 RMVar_ID_53345 Human_SNP_ID_847523938 A-to-I Human chr3 + 135925981 135925981 135925981 TCTGGGGCCTGCAGTTCTTATACAGGCCTATCACTGGATGATTGACTCCAGAGAAGACTTCACAG TCTGGGGCCTGCAGTTCTTATACAGGCCTATCGCTGGATGATTGACTCCAGAGAAGACTTCACAG A G AC092989.1 Ensembl:ENSG00000242222 Pseudogene exon GSE100210 HepG2 cell line chr3:135925980..135925981 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 1 - 53346 RMVar_ID_53346 Human_SNP_ID_847545308 A-to-I Human chr3 + 196907097 196907097 196907097 GGCCTATGGTTGTATTTACATTAGAAAAATGTAGGACAACTAGTAGAGGATTGTTCAAATTTAAA GGCCTATGGTTGTATTTACATTAGAAAAATGTGGGACAACTAGTAGAGGATTGTTCAAATTTAAA A G SENP5 Ensembl:ENSG00000119231 Protein coding intron GSE100210 HepG2 cell line chr3:196907096..196907097 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_29766,RMVar_hsa_circ_61032,RMVar_hsa_circ_223959,RMVar_hsa_circ_99857,RMVar_hsa_circ_80598,RMVar_hsa_circ_223962,RMVar_hsa_circ_76565,RMVar_hsa_circ_223966 53347 RMVar_ID_53347 Human_SNP_ID_847559707 A-to-I Human chr3 - 121523566 121523566 121523566 GGTCTATAGGTGCATGCCACCATGCCTGGCTAATTTTTTTGTATTTTTTTTTAGAGATGGGATTT GGTCTATAGGTGCATGCCACCATGCCTGGCTATTTTTTTTGTATTTTTTTTTAGAGATGGGATTT T A POLQ Ensembl:ENSG00000051341 Protein coding intron GSE38233 cultured B-cells chr3:121523565..121523566 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_27189,RMVar_hsa_circ_48738,RMVar_hsa_circ_111632,RMVar_hsa_circ_220588,RMVar_hsa_circ_52289,RMVar_hsa_circ_58205,RMVar_hsa_circ_92313,RMVar_hsa_circ_9179,RMVar_hsa_circ_36509,RMVar_hsa_circ_379115,RMVar_hsa_circ_220598,RMVar_hsa_circ_311535,RMVar_hsa_circ_24153 53348 RMVar_ID_53348 Human_SNP_ID_847726305 A-to-I Human chr3 - 113730095 113730094 113730095 GGGTTTCACCATGTTGGCCAGGCCAGTGTTGAACTCCTGGCTTCAAGTGATCCACCCGAGTCAGC GGGTTTCACCATGTTGGCCAGGCCAGTGTTGATATCCTGGCTTCAAGTGATCCACCCGAGTCAGC GT TA NAA50 Ensembl:ENSG00000121579 Protein coding intron GSE100210 HepG2 cell line chr3:113730094..113730095 29129909 RNA-Seq:(High) - Functional Loss MNV ICGC 33..34 33 MELA 1 - Human_RBP_ID_14568726 53349 RMVar_ID_53349 Human_SNP_ID_847835031 A-to-I Human chr3 - 141946946 141946946 141946946 CTCAGCCACTGCAACCTCTGCCTCCCGGGTTCAAGCGATTCTTCTGCCTCAGCCTCCCAAGTAGT CTCAGCCACTGCAACCTCTGCCTCCCGGGTTCTAGCGATTCTTCTGCCTCAGCCTCCCAAGTAGT T A TFDP2 Ensembl:ENSG00000114126 Protein coding 3'UTR GSE100210 HepG2 cell line chr3:141946945..141946946 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_7129995,Human_RBP_ID_14651566 53350 RMVar_ID_53350 Human_SNP_ID_847851111 A-to-I Human chr3 - 131478777 131478777 131478777 TTGAACCTGGGAGGTGGGGCTTGCAGTAAGCCAAGATCACACCGCTATACTCCAGCCTGGTAAAC TTGAACCTGGGAGGTGGGGCTTGCAGTAAGCCGAGATCACACCGCTATACTCCAGCCTGGTAAAC T C MRPL3 Ensembl:ENSG00000114686 Protein coding intron GSE100210 HepG2 cell line chr3:131478776..131478777 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 5 breast RMVar_hsa_circ_45611,RMVar_hsa_circ_62954,RMVar_hsa_circ_347162 53351 RMVar_ID_53351 Human_SNP_ID_847874876 A-to-I Human chr3 - 33534515 33534515 33534515 TTGCCCAGTCTGGAATGTAGTCGCTCAAACATAGCTCACTGCAGCCTTGTCCTCGTAGGCTCAAG TTGCCCAGTCTGGAATGTAGTCGCTCAAACATTGCTCACTGCAGCCTTGTCCTCGTAGGCTCAAG T A CLASP2 Ensembl:ENSG00000163539 Protein coding intron GSE107867 ASD brains,frontal_cortex chr3:33534514..33534515 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_14424,RMVar_hsa_circ_113585,RMVar_hsa_circ_304405,RMVar_hsa_circ_269578,RMVar_hsa_circ_21535,RMVar_hsa_circ_46762,RMVar_hsa_circ_18461,RMVar_hsa_circ_2032,RMVar_hsa_circ_27031,RMVar_hsa_circ_61436,RMVar_hsa_circ_216772,RMVar_hsa_circ_286425,RMVar_hsa_circ_365293,RMVar_hsa_circ_265924,RMVar_hsa_circ_41418,RMVar_hsa_circ_42018,RMVar_hsa_circ_6897,RMVar_hsa_circ_277389,RMVar_hsa_circ_216774,RMVar_hsa_circ_326669,RMVar_hsa_circ_365318,RMVar_hsa_circ_286455,RMVar_hsa_circ_111230,RMVar_hsa_circ_120430,RMVar_hsa_circ_101772,RMVar_hsa_circ_216775,RMVar_hsa_circ_216777,RMVar_hsa_circ_216778,RMVar_hsa_circ_216779,RMVar_hsa_circ_216776,RMVar_hsa_circ_6749,RMVar_hsa_circ_103703,RMVar_hsa_circ_289300,RMVar_hsa_circ_4428,RMVar_hsa_circ_216780,RMVar_hsa_circ_216781,RMVar_hsa_circ_216782 53352 RMVar_ID_53352 Human_SNP_ID_847884678 A-to-I Human chr3 - 137881634 137881634 137881634 AAACAGTTGTTATCCTTGGTCATGGCACACTCACCTTCATAAACCTGAATAAGCACACCAGGCTG AAACAGTTGTTATCCTTGGTCATGGCACACTCGCCTTCATAAACCTGAATAAGCACACCAGGCTG T C - - Other Unknown GSE100210 HepG2 cell line chr3:137881633..137881634 29129909 RNA-Seq:(High) rs878930471 Functional Loss SNV ICGC 33..33 33 LAML 1 - 53353 RMVar_ID_53353 Human_SNP_ID_847929300 A-to-I Human chr3 - 13321784 13321784 13321784 CACAATGCACAGGCTGACGGACAAGCAGCGGAAGCACCTGAGCATGAAGAAGACAGCTCTGGTGG CACAATGCACAGGCTGACGGACAAGCAGCGGACGCACCTGAGCATGAAGAAGACAGCTCTGGTGG T G NUP210 Ensembl:ENSG00000132182 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector chr3:13321783..13321784 29967493 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - Human_RBP_ID_5601975,Human_RBP_ID_14628819 Human_Splice_Rec_396548 RMVar_hsa_circ_116747,RMVar_hsa_circ_216033 53354 RMVar_ID_53354 Human_SNP_ID_847932160 A-to-I Human chr3 - 58428553 58428553 58428553 GGACATGGAAACCATAGAAGCCAGTGTCATGAAGACAAATCATCTTGTAACTGTGGAAGGAGGCT GGACATGGAAACCATAGAAGCCAGTGTCATGACGACAAATCATCTTGTAACTGTGGAAGGAGGCT T G PDHB Ensembl:ENSG00000168291 Protein coding CDS GSE100210 HepG2 cell line chr3:58428552..58428553 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_68773,Human_RBP_ID_1630614,Human_RBP_ID_1966899,Human_RBP_ID_8577407,Human_RBP_ID_9395257,Human_RBP_ID_22456805,Human_RBP_ID_22824831 Human_Splice_Rec_446920,Human_Splice_Rec_446921,Human_Splice_Rec_446936,Human_Splice_Rec_446937,Human_Splice_Rec_446954,Human_Splice_Rec_446955,Human_Splice_Rec_446974,Human_Splice_Rec_446975,Human_Splice_Rec_446984,Human_Splice_Rec_446998,Human_Splice_Rec_447014,Human_Splice_Rec_447015 RMVar_hsa_circ_219285,RMVar_hsa_circ_94286,RMVar_hsa_circ_68854 53355 RMVar_ID_53355 Human_SNP_ID_847947290 A-to-I Human chr3 - 27486549 27486549 27486549 CTTGCAGCAGTTGACAGCACGGGGGTGCAGGCAAGCATAGCACTTGCGGCAGATCATCTTGTCAC CTTGCAGCAGTTGACAGCACGGGGGTGCAGGCGAGCATAGCACTTGCGGCAGATCATCTTGTCAC T C - - Other Unknown GSE100210 HepG2 cell line chr3:27486548..27486549 29129909 RNA-Seq:(High) rs878860848 Functional Loss SNV ICGC 33..33 33 LAML 1 - 53356 RMVar_ID_53356 Human_SNP_ID_847966612 A-to-I Human chr3 + 101583916 101583916 101583916 GAACTCCTGACCTCAAGTGATCCACTTGCCTTAGCCTCCCAAAGTGCTGGGATTACAAGCATGAG GAACTCCTGACCTCAAGTGATCCACTTGCCTTGGCCTCCCAAAGTGCTGGGATTACAAGCATGAG A G PCNP Ensembl:ENSG00000081154 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr3:101583915..101583916 24183664,29129909 RNA-Seq:(High) rs935837570 Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_48579,RMVar_hsa_circ_22748,RMVar_hsa_circ_95215,RMVar_hsa_circ_220064,RMVar_hsa_circ_96179,RMVar_hsa_circ_310017,RMVar_hsa_circ_114287,RMVar_hsa_circ_220066,RMVar_hsa_circ_108674,RMVar_hsa_circ_220067,RMVar_hsa_circ_220068 53357 RMVar_ID_53357 Human_SNP_ID_848016525 A-to-I Human chr3 - 37071914 37071914 37071914 TCTTCATTGCTGTTTTGCTAAGCCTTGCAGGTAGATTCCATGTACACCAAAAGCTGGAAAAAATT TCTTCATTGCTGTTTTGCTAAGCCTTGCAGGTGGATTCCATGTACACCAAAAGCTGGAAAAAATT T C LRRFIP2 Ensembl:ENSG00000093167 Protein coding intron GSE38233 cultured B-cells chr3:37071913..37071914 24183664 RNA-Seq:(High) rs17810211 Functional Loss SNV ICGC 33..33 33 SKCA 1 - RMVar_hsa_circ_28392,RMVar_hsa_circ_216982,RMVar_hsa_circ_307497,RMVar_hsa_circ_366508,RMVar_hsa_circ_368143,RMVar_hsa_circ_321277,RMVar_hsa_circ_72192,RMVar_hsa_circ_319873,RMVar_hsa_circ_70467,RMVar_hsa_circ_38058,RMVar_hsa_circ_115564,RMVar_hsa_circ_216983,RMVar_hsa_circ_216984 53358 RMVar_ID_53358 Human_SNP_ID_848102205 A-to-I Human chr3 + 49989742 49989742 49989742 TTCCCCAAAAAGTTGCTAACAGACGTTATTTTATTTTATTTATTTATTTTGATACAGAGTCTCTC TTCCCCAAAAAGTTGCTAACAGACGTTATTTTGTTTTATTTATTTATTTTGATACAGAGTCTCTC A G RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE100210 HepG2 cell line chr3:49989741..49989742 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_7248559 RMVar_hsa_circ_15596,RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_54905,RMVar_hsa_circ_280801,RMVar_hsa_circ_368344,RMVar_hsa_circ_306069,RMVar_hsa_circ_350418,RMVar_hsa_circ_218309,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_290547,RMVar_hsa_circ_306473,RMVar_hsa_circ_68132,RMVar_hsa_circ_218313,RMVar_hsa_circ_218311,RMVar_hsa_circ_218312,RMVar_hsa_circ_334070 53359 RMVar_ID_53359 Human_SNP_ID_848102427 A-to-I Human chr3 - 48528622 48528622 48528622 GGTCTTGCTTTGTTGCCCAGGCTGAGTGCAGTAGCACGATCTTAGCTCACTGCAGCCTCCATCTC GGTCTTGCTTTGTTGCCCAGGCTGAGTGCAGTGGCACGATCTTAGCTCACTGCAGCCTCCATCTC T C PFKFB4 Ensembl:ENSG00000114268 Protein coding intron GSE38233 cultured B-cells chr3:48528621..48528622 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_338662,RMVar_hsa_circ_267763 53360 RMVar_ID_53360 Human_SNP_ID_848116523 A-to-I Human chr3 + 159284711 159284711 159284711 TAGAGATTGGGTTTCATCATGTTGGCCAGGCTAGTCTCGAACTTGTGACCTCAGATGATCTGCTT TAGAGATTGGGTTTCATCATGTTGGCCAGGCTGGTCTCGAACTTGTGACCTCAGATGATCTGCTT A G IQCJ-SCHIP1 Ensembl:ENSG00000283154 Protein coding intron GSE107867 ASD brains,frontal_cortex chr3:159284710..159284711 30559470 RNA-Seq:(High) rs1199993380 Functional Loss SNV ICGC 33..33 33 MALY 1 - 53361 RMVar_ID_53361 Human_SNP_ID_848183252 A-to-I Human chr3 - 178997687 178997687 178997687 AACCAGCTCAGAGGACCCTCTGCCTTTTTGCAAAGGCAGAGGGCCAATGTGACAGCTTTCCGTAT AACCAGCTCAGAGGACCCTCTGCCTTTTTGCAGAGGCAGAGGGCCAATGTGACAGCTTTCCGTAT T C ZMAT3 Ensembl:ENSG00000172667 Protein coding intron GSE100210 HepG2 cell line chr3:178997686..178997687 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 53362 RMVar_ID_53362 Human_SNP_ID_848258237 A-to-I Human chr3 - 125460046 125460046 125460046 GGGATTACAGGCGCCCGCCAACACACCCAGCTAATTTTTGTATTTTTAGTAGAGACAGGGTTTCA GGGATTACAGGCGCCCGCCAACACACCCAGCTGATTTTTGTATTTTTAGTAGAGACAGGGTTTCA T C SNX4 Ensembl:ENSG00000114520 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr3:125460045..125460046 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_3042,RMVar_hsa_circ_220892,RMVar_hsa_circ_266705,RMVar_hsa_circ_301967,RMVar_hsa_circ_330096,RMVar_hsa_circ_91232,RMVar_hsa_circ_220893,RMVar_hsa_circ_8244,RMVar_hsa_circ_38805,RMVar_hsa_circ_220894,RMVar_hsa_circ_220898,RMVar_hsa_circ_105641,RMVar_hsa_circ_360162,RMVar_hsa_circ_282808,RMVar_hsa_circ_220899,RMVar_hsa_circ_41436,RMVar_hsa_circ_303263,RMVar_hsa_circ_13062,RMVar_hsa_circ_220900 53363 RMVar_ID_53363 Human_SNP_ID_848285677 A-to-I Human chr3 - 48078229 48078223 48078229 GAGGTGGGAGGATCATTCACTTGAGCCAAAGAATTTGAGATTGCAGTGAGCCATGATCGTGCACT GAGGTGGGAGGATCATTCACTTGAGCCAAAGA______GATTGCAGTGAGCCATGATCGTGCACT CTCAAAT C MAP4 Ensembl:ENSG00000047849 Protein coding intron GSE100210 HepG2 cell line chr3:48078228..48078229 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 33..38 33 PEME 1 - Human_RBP_ID_14855173,Human_RBP_ID_25740527 53364 RMVar_ID_53364 Human_SNP_ID_848373210 A-to-I Human chr3 - 15072908 15072908 15072908 GAGATCGAGACCACCCTGGCTAACACAGTGAAATCCCGTCTCTACTAAAAATACAAAAAATTAGC GAGATCGAGACCACCCTGGCTAACACAGTGAAGTCCCGTCTCTACTAAAAATACAAAAAATTAGC T C RBSN Ensembl:ENSG00000131381 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells chr3:15072907..15072908 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_miRNA_ID_1221105,Human_miRNA_ID_1390861,Human_miRNA_ID_2377481,Human_miRNA_ID_3092556 RMVar_hsa_circ_100635,RMVar_hsa_circ_216128 53365 RMVar_ID_53365 Human_SNP_ID_848377563 A-to-I Human chr3 + 183769717 183769716 183769718 CTGTTTTCATTTTATTTATTTATTGTTTAGACAGAGTCTTGCTCTGTCGCCAGGCTAGAGTGCAG CTGTTTTCATTTTATTTATTTATTGTTTAGAC__AGTCTTGCTCTGTCGCCAGGCTAGAGTGCAG CAG C YEATS2 Ensembl:ENSG00000163872 Protein coding intron GSE38233 cultured B-cells chr3:183769716..183769717 24183664 RNA-Seq:(High) rs545847957 Functional Loss DEL ICGC 33..34 33 PBCA 1 - RMVar_hsa_circ_3315,RMVar_hsa_circ_268404,RMVar_hsa_circ_9195,RMVar_hsa_circ_74353,RMVar_hsa_circ_357245,RMVar_hsa_circ_374779,RMVar_hsa_circ_307692,RMVar_hsa_circ_96889,RMVar_hsa_circ_62303,RMVar_hsa_circ_223165,RMVar_hsa_circ_223166,RMVar_hsa_circ_18836,RMVar_hsa_circ_77641,RMVar_hsa_circ_114457,RMVar_hsa_circ_223175,RMVar_hsa_circ_223176,RMVar_hsa_circ_76043,RMVar_hsa_circ_295617,RMVar_hsa_circ_38709,RMVar_hsa_circ_99840,RMVar_hsa_circ_48728,RMVar_hsa_circ_120074,RMVar_hsa_circ_223184,RMVar_hsa_circ_223183,RMVar_hsa_circ_303412,RMVar_hsa_circ_283070,RMVar_hsa_circ_103962,RMVar_hsa_circ_116923,RMVar_hsa_circ_86944,RMVar_hsa_circ_26433,RMVar_hsa_circ_223191,RMVar_hsa_circ_223195,RMVar_hsa_circ_18261,RMVar_hsa_circ_223193,RMVar_hsa_circ_223194,RMVar_hsa_circ_223192,RMVar_hsa_circ_52360,RMVar_hsa_circ_223190,RMVar_hsa_circ_352913,RMVar_hsa_circ_223200,RMVar_hsa_circ_49691,RMVar_hsa_circ_71679,RMVar_hsa_circ_122361,RMVar_hsa_circ_377071,RMVar_hsa_circ_105810,RMVar_hsa_circ_117039,RMVar_hsa_circ_223202,RMVar_hsa_circ_223204,RMVar_hsa_circ_223203,RMVar_hsa_circ_127150,RMVar_hsa_circ_348578,RMVar_hsa_circ_372828,RMVar_hsa_circ_223201,RMVar_hsa_circ_223209,RMVar_hsa_circ_223211,RMVar_hsa_circ_111494,RMVar_hsa_circ_223212,RMVar_hsa_circ_223210,RMVar_hsa_circ_28287,RMVar_hsa_circ_344788,RMVar_hsa_circ_223208,RMVar_hsa_circ_223217,RMVar_hsa_circ_64448,RMVar_hsa_circ_350603,RMVar_hsa_circ_363489,RMVar_hsa_circ_47480 53366 RMVar_ID_53366 Human_SNP_ID_848398507 A-to-I Human chr3 - 33428173 33428173 33428173 TCTTTTTTTTTTTTTTTTTTTTTTGAGATGGAATCTCGCTCTGTCACTGAGGCTGGAGTGCAGTG TCTTTTTTTTTTTTTTTTTTTTTTGAGATGGAGTCTCGCTCTGTCACTGAGGCTGGAGTGCAGTG T C UBP1 Ensembl:ENSG00000153560 Protein coding intron GSE100210 HepG2 cell line chr3:33428172..33428173 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_116873,RMVar_hsa_circ_216752,RMVar_hsa_circ_126430,RMVar_hsa_circ_216757,RMVar_hsa_circ_105056,RMVar_hsa_circ_116582,RMVar_hsa_circ_216765,RMVar_hsa_circ_216767,RMVar_hsa_circ_98989,RMVar_hsa_circ_216766 53367 RMVar_ID_53367 Human_SNP_ID_848436316 A-to-I Human chr3 - 47447602 47447602 47447602 CTCACTGTGGCCTCCGCCTCCCGGGTTTAAGCAATTCTCCTGTCTCCGCCTCCCAAGTAGCTGGT CTCACTGTGGCCTCCGCCTCCCGGGTTTAAGCGATTCTCCTGTCTCCGCCTCCCAAGTAGCTGGT T C SCAP Ensembl:ENSG00000114650 Protein coding intron GSE100210 HepG2 cell line chr3:47447601..47447602 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - RMVar_hsa_circ_112004,RMVar_hsa_circ_217598,RMVar_hsa_circ_101506,RMVar_hsa_circ_217617,RMVar_hsa_circ_217618,RMVar_hsa_circ_217619 53368 RMVar_ID_53368 Human_SNP_ID_848455483 A-to-I Human chr3 + 47186755 47186755 47186755 GTGGTGGCTCATGCCTGTAATCCCAGCACTTTAGGAGGCCAAGGCAGGTGGACAACTTGAGGCCA GTGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCAGGTGGACAACTTGAGGCCA A G KIF9-AS1 Ensembl:ENSG00000227398 lincRNA intron GSE100210 HepG2 cell line chr3:47186754..47186755 29129909 RNA-Seq:(High) rs374291008 Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_82426,RMVar_hsa_circ_217555 53369 RMVar_ID_53369 Human_SNP_ID_848537271 A-to-I Human chr3 - 62438132 62438132 62438132 TTCTCAGGATGTCCTGCGTGATAAGGTCAATGAGGAGATGTACATAGAAAGGTTATTTGATGTAA TTCTCAGGATGTCCTGCGTGATAAGGTCAATGGGGAGATGTACATAGAAAGGTTATTTGATGTAA T C CADPS Ensembl:ENSG00000163618 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr3:62438131..62438132 30559470 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue Burkitt_lymphoma 10 haematopoietic and lymphoid tissue Human_Splice_Rec_448154,Human_Splice_Rec_448155,Human_Splice_Rec_448174,Human_Splice_Rec_448175,Human_Splice_Rec_448230,Human_Splice_Rec_448231,Human_Splice_Rec_448282,Human_Splice_Rec_448283,Human_Splice_Rec_448287,Human_Splice_Rec_448300,Human_Splice_Rec_448301,Human_Splice_Rec_448352,Human_Splice_Rec_448353,Human_Splice_Rec_448364,Human_Splice_Rec_448365 RMVar_hsa_circ_219350,RMVar_hsa_circ_61904,RMVar_hsa_circ_312404,RMVar_hsa_circ_7729,RMVar_hsa_circ_327002,RMVar_hsa_circ_341371,RMVar_hsa_circ_325765,RMVar_hsa_circ_304942,RMVar_hsa_circ_306861,RMVar_hsa_circ_275652,RMVar_hsa_circ_219352,RMVar_hsa_circ_219353,RMVar_hsa_circ_219354,RMVar_hsa_circ_219351 53370 RMVar_ID_53370 Human_SNP_ID_848541897 A-to-I Human chr3 - 44578313 44578313 44578313 AGGATGCCTATGAACTAGAAGTCTTATTGCGGATATAGGAATCGGAAATACAGTACCTGAAACAG AGGATGCCTATGAACTAGAAGTCTTATTGCGGGTATAGGAATCGGAAATACAGTACCTGAAACAG T C ZKSCAN7-AS1 Ensembl:ENSG00000236869 lincRNA intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr3:44578312..44578313 24183664,29129909 RNA-Seq:(High) rs1488909418 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 haematopoietic and lymphoid tissue Human_RBP_ID_5604385 53371 RMVar_ID_53371 Human_SNP_ID_848557207 A-to-I Human chr3 + 136331803 136331800 136331803 ATTTATTTTATTTTATTTATTTATTTTTTGAGAAGGAGTCTCGCTCTGTCGCCAGGCTGGAGTGC ATTTATTTTATTTTATTTATTTATTTTTTG___AGGAGTCTCGCTCTGTCGCCAGGCTGGAGTGC GAGA G PCCB Ensembl:ENSG00000114054 Protein coding intron GSE100210 HepG2 cell line chr3:136331802..136331803;chr3:136331803..136331804 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 31..33 33 ESCA 1 - 53372 RMVar_ID_53372 Human_SNP_ID_848572080 A-to-I Human chr3 + 141890571 141890571 141890571 GTGATCTGCCCGCCTCAGCCTCCCACAGTGCTAGGATTACAGGCGTGAGCCACCACGCCCACCTA GTGATCTGCCCGCCTCAGCCTCCCACAGTGCTGGGATTACAGGCGTGAGCCACCACGCCCACCTA A G ATP1B3 Ensembl:ENSG00000069849 Protein coding intron GSE100210 HepG2 cell line chr3:141890570..141890571 29129909 RNA-Seq:(High) rs1455169925 Functional Loss SNV ICGC 33..33 33 LAML 1 - 53373 RMVar_ID_53373 Human_SNP_ID_848721130 A-to-I Human chr3 + 40537440 40537439 40537440 CTTGGGCCACAAAGTGAGACCCCTGTCTCTACAAAAAATTAAAAATTTAGCTGGGTGTGGTTGTG CTTGGGCCACAAAGTGAGACCCCTGTCTCTAC_AAAAATTAAAAATTTAGCTGGGTGTGGTTGTG CA C ZNF621 Ensembl:ENSG00000172888 Protein coding intron GSE38233;GSE100210;GSE99789;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490832,GSM3490833,GSM3490834;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,KYSE180 cell line;esophageal squamous carcinoma cells,KYSE180 cell line chr3:40537440..40537441;chr3:40537439..40537440 24183664,29129909,29796672,29796672,31158229,31158229,31158229,31158229,31158229,31158229,32596459,32596459 RNA-Seq:(High) - Functional Loss DEL ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_217161,RMVar_hsa_circ_126844 53374 RMVar_ID_53374 Human_SNP_ID_848751029 A-to-I Human chr3 + 124452463 124452463 124452463 AGACTTATAAATAATGTGATGTATGCTAAAATAGAAGCATGTATGTGATACTGTGGGAACACTGG AGACTTATAAATAATGTGATGTATGCTAAAATGGAAGCATGTATGTGATACTGTGGGAACACTGG A G KALRN Ensembl:ENSG00000160145 Protein coding intron GSE107867 ASD brains,temporal_cortex chr3:124452462..124452463 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - RMVar_hsa_circ_33119,RMVar_hsa_circ_302640,RMVar_hsa_circ_15830,RMVar_hsa_circ_378149,RMVar_hsa_circ_45695,RMVar_hsa_circ_220793,RMVar_hsa_circ_35224,RMVar_hsa_circ_323158,RMVar_hsa_circ_63800,RMVar_hsa_circ_38424,RMVar_hsa_circ_42981,RMVar_hsa_circ_220801,RMVar_hsa_circ_52943,RMVar_hsa_circ_220802,RMVar_hsa_circ_220806,RMVar_hsa_circ_19452,RMVar_hsa_circ_220804,RMVar_hsa_circ_126238,RMVar_hsa_circ_220805,RMVar_hsa_circ_327151,RMVar_hsa_circ_266040,RMVar_hsa_circ_220807 53375 RMVar_ID_53375 Human_SNP_ID_848781550 A-to-I Human chr3 - 124979039 124979039 124979039 AGGCTGAGGCAGAAGAATCGCTTGAACCCAGGAGGTGGAGGTTCAGTGAGCCGGGATCGCACCAT AGGCTGAGGCAGAAGAATCGCTTGAACCCAGGGGGTGGAGGTTCAGTGAGCCGGGATCGCACCAT T C HEG1 Ensembl:ENSG00000173706 Protein coding intron GSE100210 HepG2 cell line chr3:124979038..124979039 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 2 liver RMVar_hsa_circ_8589,RMVar_hsa_circ_87104,RMVar_hsa_circ_265500,RMVar_hsa_circ_220847,RMVar_hsa_circ_269564,RMVar_hsa_circ_220849 53376 RMVar_ID_53376 Human_SNP_ID_848805556 A-to-I Human chr3 - 184349531 184349531 184349531 ATGGTGGTGGGCACCTGTAGTCCAAGCTACTCAGGAGGCTGAGGTGGGAGGACTGCACGAGCCCA ATGGTGGTGGGCACCTGTAGTCCAAGCTACTCGGGAGGCTGAGGTGGGAGGACTGCACGAGCCCA T C CLCN2 Ensembl:ENSG00000114859 Protein coding intron GSE100210 HepG2 cell line chr3:184349530..184349531 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 COCA 1 - 53377 RMVar_ID_53377 Human_SNP_ID_848814013 A-to-I Human chr3 + 69812886 69812878 69812887 GGGCAATGGGAAAGGTTTACAATTGGAAAGGAAAGTTGGTGTAGGTCTTTCCAGCAGTAAAATCT GGGCAATGGGAAAGGTTTACAATTG_________GTTGGTGTAGGTCTTTCCAGCAGTAAAATCT GGAAAGGAAA G MITF Ensembl:ENSG00000187098 Protein coding intron GSE100210 HepG2 cell line chr3:69812886..69812887 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 26..34 33 RECA 1 - RMVar_hsa_circ_368653 53378 RMVar_ID_53378 Human_SNP_ID_848879070 A-to-I Human chr3 - 65987625 65987625 65987625 ATGCCATTGCACTCCAGCCTGGGTGACAGAGTAAGACTCTGCCTTAAAAAAGAAAGGAAAGAAAA ATGCCATTGCACTCCAGCCTGGGTGACAGAGTGAGACTCTGCCTTAAAAAAGAAAGGAAAGAAAA T C MAGI1 Ensembl:ENSG00000151276 Protein coding intron GSE107867 ASD brains,cerebellum chr3:65987624..65987625 30559470 RNA-Seq:(High) rs1026242350 Functional Loss SNV ICGC 33..33 33 STAD 1 - RMVar_hsa_circ_106022,RMVar_hsa_circ_219443,RMVar_hsa_circ_87074,RMVar_hsa_circ_219454 53379 RMVar_ID_53379 Human_SNP_ID_848888986 A-to-I Human chr3 - 47508913 47508913 47508913 AAACATACGAAAAATTAGCTGGGCATGGTGGCAGGCGCCTGTAGTCCCAGGTACTTGGGAGACTG AAACATACGAAAAATTAGCTGGGCATGGTGGCGGGCGCCTGTAGTCCCAGGTACTTGGGAGACTG T C ELP6 Ensembl:ENSG00000163832 Protein coding intron GSE38233 cultured B-cells chr3:47508912..47508913 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - RMVar_hsa_circ_128056,RMVar_hsa_circ_217623,RMVar_hsa_circ_319812,RMVar_hsa_circ_217626,RMVar_hsa_circ_316161,RMVar_hsa_circ_217629,RMVar_hsa_circ_217627,RMVar_hsa_circ_305483,RMVar_hsa_circ_314638,RMVar_hsa_circ_217630 53380 RMVar_ID_53380 Human_SNP_ID_848973774 A-to-I Human chr3 + 159475871 159475871 159475871 GAAACAGGAATTAAGGCAAAAGTTATGGCAGGAGTTGAAGCTTTCATAACAAGGTCTTGGGAAAA GAAACAGGAATTAAGGCAAAAGTTATGGCAGGGGTTGAAGCTTTCATAACAAGGTCTTGGGAAAA A G IQCJ-SCHIP1 Ensembl:ENSG00000283154 Protein coding intron GSE107867 ASD brains,frontal_cortex chr3:159475870..159475871 30559470 RNA-Seq:(High) rs1373787196 Functional Loss SNV ICGC 33..33 33 SKCA 3 - Human_RBP_ID_9134601 RMVar_hsa_circ_222402 53381 RMVar_ID_53381 Human_SNP_ID_849016221 A-to-I Human chr3 + 10275079 10275079 10275079 ATGATCTCAGCTCACTGCAGCCTTTGCCTCCCAGGTTCAGGGGATTCTCCTGCCTCAGCCACCCA ATGATCTCAGCTCACTGCAGCCTTTGCCTCCCGGGTTCAGGGGATTCTCCTGCCTCAGCCACCCA A G TATDN2,AC022384.1 Ensembl:ENSG00000157014,Ensembl:ENSG00000272410 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells chr3:10275078..10275079 24183664 RNA-Seq:(High) rs1006162486 Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_215827,RMVar_hsa_circ_101231,RMVar_hsa_circ_334876 53382 RMVar_ID_53382 Human_SNP_ID_849036791 A-to-I Human chr3 + 72979750 72979750 72979750 TCAGCTCACTGCAGCCTCCGCCTCCCAGGTTCAAACGATTCTCATGCCTCAGGCTTCCGAGTAGC TCAGCTCACTGCAGCCTCCGCCTCCCAGGTTCGAACGATTCTCATGCCTCAGGCTTCCGAGTAGC A G GXYLT2 Ensembl:ENSG00000172986 Protein coding intron GSE100210 HepG2 cell line chr3:72979750..72979751 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_20950098 53383 RMVar_ID_53383 Human_SNP_ID_849045359 A-to-I Human chr3 - 28331916 28331916 28331916 TATCTGTAGCACAGCCTGGAGTGCAGTGGCGCAATCATGGGATAGCATGAATTTTGAGGACTGTT TATCTGTAGCACAGCCTGGAGTGCAGTGGCGCGATCATGGGATAGCATGAATTTTGAGGACTGTT T C AZI2 Ensembl:ENSG00000163512 Protein coding intron GSE100210 HepG2 cell line chr3:28331915..28331916 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 oesophagus squamous_cell_carcinoma 4 oesophagus Human_RBP_ID_7185265,Human_RBP_ID_10092687,Human_RBP_ID_14785830 Human_Splice_Rec_404606,Human_Splice_Rec_404610,Human_Splice_Rec_404612,Human_Splice_Rec_404624,Human_Splice_Rec_404638 RMVar_hsa_circ_87680,RMVar_hsa_circ_61704,RMVar_hsa_circ_216568 53384 RMVar_ID_53384 Human_SNP_ID_849048753 A-to-I Human chr3 - 96350556 96350556 96350556 CAAGTTTCATCAGCACTGAAACCAACCATGCCATGGTAACAGTCTCCAGGTCTCCCTCTTCTGTC CAAGTTTCATCAGCACTGAAACCAACCATGCCGTGGTAACAGTCTCCAGGTCTCCCTCTTCTGTC T C lnc-MTRNR2L12-9 RNACentral:URS00009BA044 lincRNA exon GSE100210 HepG2 cell line chr3:96350555..96350556 29129909 RNA-Seq:(High) rs879110177 Functional Loss SNV ICGC 33..33 33 LAML 2 - 53385 RMVar_ID_53385 Human_SNP_ID_849116451 A-to-I Human chr3 + 23848259 23848259 23848259 GGGAGGCCAAGGCGGATGGATCACTTGAGGTCAGGAGTTTGAGACCAGCCTGGCCAACATGATGA GGGAGGCCAAGGCGGATGGATCACTTGAGGTCGGGAGTTTGAGACCAGCCTGGCCAACATGATGA A G UBE2E1 Ensembl:ENSG00000170142 Protein coding intron GSE38233 cultured B-cells chr3:23848258..23848259 24183664 RNA-Seq:(High) rs780917494 Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_358580 53386 RMVar_ID_53386 Human_SNP_ID_849213483 A-to-I Human chr3 + 197884418 197884418 197884418 ACTTCAAGTGATCCACCTGCCTCGGCCTCCCAAAATGCTGGGATTACAGGCGTGAGCCACTGTGC ACTTCAAGTGATCCACCTGCCTCGGCCTCCCAGAATGCTGGGATTACAGGCGTGAGCCACTGTGC A G LRCH3 Ensembl:ENSG00000186001 Protein coding 3'UTR GSE38233 cultured B-cells chr3:197884418..197884419 24183664 RNA-Seq:(High) rs1316295707 Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 3 pancreas Human_RBP_ID_17573974 53387 RMVar_ID_53387 Human_SNP_ID_849238184 A-to-I Human chr3 + 45204602 45204602 45204602 GCAATCATAGCTCACTGCAACCTTCACCTCCCAGGCTTAAGCAATCCTCCCACCTCAGCCTCCCA GCAATCATAGCTCACTGCAACCTTCACCTCCCGGGCTTAAGCAATCCTCCCACCTCAGCCTCCCA A G - - Other Unknown GSE100210 HepG2 cell line chr3:45204601..45204602 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 53388 RMVar_ID_53388 Human_SNP_ID_849244107 A-to-I Human chr3 + 184149747 184149747 184149747 AATTTCCAAGAAGAGGATGTTTGTCACTGATGACATCTTCAAAGCTGAACTGAATGAGTTTCTTA AATTTCCAAGAAGAGGATGTTTGTCACTGATGGCATCTTCAAAGCTGAACTGAATGAGTTTCTTA A G AC131235.2 Ensembl:ENSG00000228205 Pseudogene exon GSE100210 HepG2 cell line chr3:184149746..184149747 29129909 RNA-Seq:(High) rs878876281 Functional Loss SNV ICGC 33..33 33 LAML 1 - 53389 RMVar_ID_53389 Human_SNP_ID_849257078 A-to-I Human chr3 + 101824627 101824627 101824627 ACCATGCCCAGCTAATTTTTGTATCTTTTTGTAGAGACTACATTTTGCCATGTTGTCCAGGCTGG ACCATGCCCAGCTAATTTTTGTATCTTTTTGTTGAGACTACATTTTGCCATGTTGTCCAGGCTGG A T NXPE3 Ensembl:ENSG00000144815 Protein coding 3'UTR GSE100210;GSE107867 HepG2 cell line;ASD brains,cerebellum chr3:101824626..101824627 29129909,30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - RMVar_hsa_circ_220115,RMVar_hsa_circ_266658 53390 RMVar_ID_53390 Human_SNP_ID_849338367 A-to-I Human chr3 + 68145352 68145352 68145352 TGGAAGCACTTAGAGATGCAACAAGGAGACGCACCTTTGCCCTGGTCTCTCAAGCATATACTTCA TGGAAGCACTTAGAGATGCAACAAGGAGACGCGCCTTTGCCCTGGTCTCTCAAGCATATACTTCA A G COPS8P2,TAFA1 Ensembl:ENSG00000214552,Ensembl:ENSG00000183662 Pseudogene,Protein coding exon,intron GSE100210 HepG2 cell line chr3:68145351..68145352 29129909 RNA-Seq:(High) rs11553714 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 haematopoietic and lymphoid tissue Human_RBP_ID_7237480,Human_RBP_ID_17405137 Human_miRNA_ID_1834671,Human_miRNA_ID_1834777,Human_miRNA_ID_1879290 53391 RMVar_ID_53391 Human_SNP_ID_849365747 A-to-I Human chr3 - 194482755 194482755 194482755 TGCCCAGGCTTGTCTCAGAACTCCTGGCCTCAAGTGATCCTCCTGCCTCAGCCTCCCAAAGTGTA TGCCCAGGCTTGTCTCAGAACTCCTGGCCTCACGTGATCCTCCTGCCTCAGCCTCCCAAAGTGTA T G ATP13A3 Ensembl:ENSG00000133657 Protein coding intron GSE100210 HepG2 cell line chr3:194482754..194482755 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_14758286 53392 RMVar_ID_53392 Human_SNP_ID_849394763 A-to-I Human chr3 + 58318816 58318816 58318816 GAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGTGAAACCCCATCTCTACTAAAAATACAAAA GAGGTCAGGAGTTCAAGACCAGCCTGGCCAACGTGTGAAACCCCATCTCTACTAAAAATACAAAA A G RPP14 Ensembl:ENSG00000163684 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells chr3:58318815..58318816 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 3 oesophagus Human_Splice_Rec_446510 RMVar_hsa_circ_219276,RMVar_hsa_circ_96723 53393 RMVar_ID_53393 Human_SNP_ID_849411407 A-to-I Human chr3 - 27455850 27455850 27455850 AGGTTTTGTTTTTTGTGTTTTTTTTTGAGACAAGGTCTCGTTCTGTTGCCCAGGCTAGAGTGCGG AGGTTTTGTTTTTTGTGTTTTTTTTTGAGACAGGGTCTCGTTCTGTTGCCCAGGCTAGAGTGCGG T C SLC4A7 Ensembl:ENSG00000033867 Protein coding intron GSE100210 HepG2 cell line chr3:27455849..27455850 29129909 RNA-Seq:(High) rs991517853 Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_3704375,Human_RBP_ID_14784279 RMVar_hsa_circ_100194,RMVar_hsa_circ_216560 53394 RMVar_ID_53394 Human_SNP_ID_849474817 A-to-I Human chr3 + 57568202 57568202 57568202 TAATTAAATTTGGGCAAGGCAGAGTGGCTCATACCTGTAATCCCAGCACTTTGGGAGGCCTAGGT TAATTAAATTTGGGCAAGGCAGAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCTAGGT A G - - Other Unknown GSE100210 HepG2 cell line chr3:57568201..57568202 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - Human_RBP_ID_8577105 53395 RMVar_ID_53395 Human_SNP_ID_849488605 A-to-I Human chr3 - 94076151 94076151 94076151 TTCCAGTGGTACTGATCGCAGACTGAATGTCTAGGATTTAAGTAAAATTGGAGAGGAACAATCCC TTCCAGTGGTACTGATCGCAGACTGAATGTCTGGGATTTAAGTAAAATTGGAGAGGAACAATCCC T C RBBP4P2 Ensembl:ENSG00000242457 Pseudogene exon GSE107867 ASD brains,cerebellum chr3:94076150..94076151 30559470 RNA-Seq:(High) rs1443813115 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue Human_miRNA_ID_1887024 53396 RMVar_ID_53396 Human_SNP_ID_849529284 A-to-I Human chr3 + 10150912 10150912 10150912 TTGTTGTTGTTTTGTTTTGTTTTGTTTTTTTGAGATGGAGTCTCACTCTTGTCACCCAGGCTGGA TTGTTGTTGTTTTGTTTTGTTTTGTTTTTTTGGGATGGAGTCTCACTCTTGTCACCCAGGCTGGA A G VHL Ensembl:ENSG00000134086 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr3:10150911..10150912 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 2 kidney Human_RBP_ID_22371893 Human_miRNA_ID_266180,Human_miRNA_ID_1102323,Human_miRNA_ID_1529605,Human_miRNA_ID_1537418 53397 RMVar_ID_53397 Human_SNP_ID_849530224 A-to-I Human chr3 - 195711066 195711066 195711066 CCAGGAGCCAGGTCCCTCCATACCTCATCTCAATTAACTCACTCACCAGGAGCCAGGTCCCTCCA CCAGGAGCCAGGTCCCTCCATACCTCATCTCAGTTAACTCACTCACCAGGAGCCAGGTCCCTCCA T C lnc-MUC4-2-001,lnc-MUC4-2-001:2,lnc-MUC4-2-002 RNACentral:URS00008C3B28,RNACentral:URS00008B2B8D,RNACentral:URS00008B8242 lincRNA,lincRNA,lincRNA exon,exon,intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank chr3:195711065..195711066 30559470 RNA-Seq:(High) rs1285708678 Functional Loss SNV ICGC 33..33 33 LAML 1 - 53398 RMVar_ID_53398 Human_SNP_ID_849553982 A-to-I Human chr3 - 94059382 94059382 94059382 TGGTGGAGCCCTGTCTCTACAGAAGATACAAAAATTGGCTGGGCATTGTGGCACACACCTGTAGT TGGTGGAGCCCTGTCTCTACAGAAGATACAAATATTGGCTGGGCATTGTGGCACACACCTGTAGT T A DHFR2 Ensembl:ENSG00000178700 Protein coding intron GSE47997 K562 cells&HepG2 cells chr3:94059381..94059382 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 4 pancreas 53399 RMVar_ID_53399 Human_SNP_ID_849580774 A-to-I Human chr3 + 179337546 179337545 179337546 TTTAATAGAGACGGGGTTTCACCATGTTGACCAGGCTGGTCTTGAACTCCTGACCTCTTGTGATC TTTAATAGAGACGGGGTTTCACCATGTTGACC_GGCTGGTCTTGAACTCCTGACCTCTTGTGATC CA C ZNF639 Ensembl:ENSG00000121864 Protein coding 3'UTR GSE100210 HepG2 cell line chr3:179337545..179337546 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 33..33 33 LMS 1 - RMVar_hsa_circ_222893 53400 RMVar_ID_53400 Human_SNP_ID_849601967 A-to-I Human chr3 + 196922695 196922695 196922695 CAGGCTGGAGTGCAGTGGTGCAATCTCTGCTCAGTGCAACCTCCGCCTCCCAGGCTCAAGCCATC CAGGCTGGAGTGCAGTGGTGCAATCTCTGCTCGGTGCAACCTCCGCCTCCCAGGCTCAAGCCATC A G SENP5 Ensembl:ENSG00000119231 Protein coding intron GSE100210 HepG2 cell line chr3:196922694..196922695 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 COCA 1 - RMVar_hsa_circ_29766,RMVar_hsa_circ_61032,RMVar_hsa_circ_223959,RMVar_hsa_circ_99857,RMVar_hsa_circ_80598,RMVar_hsa_circ_223962,RMVar_hsa_circ_76565,RMVar_hsa_circ_223966 53401 RMVar_ID_53401 Human_SNP_ID_849650829 A-to-I Human chr3 - 137881638 137881638 137881638 TGCCAAACAGTTGTTATCCTTGGTCATGGCACACTCACCTTCATAAACCTGAATAAGCACACCAG TGCCAAACAGTTGTTATCCTTGGTCATGGCACGCTCACCTTCATAAACCTGAATAAGCACACCAG T C - - Other Unknown GSE100210 HepG2 cell line chr3:137881637..137881638 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 1 - 53402 RMVar_ID_53402 Human_SNP_ID_849653240 A-to-I Human chr3 + 9998963 9998963 9998963 CAATTTTGGTAGACATAAGGTTTCGTCATGTTACCCAGACTGGTCTCGAACTTTTGAGCTTAGGA CAATTTTGGTAGACATAAGGTTTCGTCATGTTCCCCAGACTGGTCTCGAACTTTTGAGCTTAGGA A C EMC3-AS1 Ensembl:ENSG00000180385 Pseudogene intron GSE100210 HepG2 cell line chr3:9998962..9998963 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_1383185,Human_RBP_ID_7097176,Human_RBP_ID_8264734,Human_RBP_ID_14544895,Human_RBP_ID_18517213,Human_RBP_ID_18536582,Human_RBP_ID_23188076 RMVar_hsa_circ_107386,RMVar_hsa_circ_215751 53403 RMVar_ID_53403 Human_SNP_ID_849730156 A-to-I Human chr3 - 11216434 11216434 11216434 ATATCACAGGATTTCCTTTCTTTTGGATGCTGAATAATATTTTATTGTATGAATACGCCACATTT ATATCACAGGATTTCCTTTCTTTTGGATGCTGGATAATATTTTATTGTATGAATACGCCACATTT T C AC083855.2 Ensembl:ENSG00000285906 lincRNA intron GSE100210 HepG2 cell line chr3:11216433..11216434 29129909 RNA-Seq:(High) rs1241114737 Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 3 oesophagus 53404 RMVar_ID_53404 Human_SNP_ID_849766118 A-to-I Human chr3 - 114965544 114965544 114965544 GGATTTTTAAGTGAAATAAGCCAGGTACAGAAAGACAAATGCTGCATGATCTCACTTATATGTGG GGATTTTTAAGTGAAATAAGCCAGGTACAGAAGGACAAATGCTGCATGATCTCACTTATATGTGG T C ZBTB20 Ensembl:ENSG00000181722 Protein coding intron GSE107867 ASD brains,cerebellum chr3:114965543..114965544 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 3 prostate 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 53405 RMVar_ID_53405 Human_SNP_ID_849854225 A-to-I Human chr3 + 50035863 50035863 50035863 GCTCACTGCAACCTCCCCTCCCAGGTTCAAGCAATTCTCGTGCCTCAGCCTCCTGAGTAGCTGGG GCTCACTGCAACCTCCCCTCCCAGGTTCAAGCGATTCTCGTGCCTCAGCCTCCTGAGTAGCTGGG A G RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE38233 cultured B-cells chr3:50035863..50035864 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 5 prostate RMVar_hsa_circ_15596,RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_280801,RMVar_hsa_circ_350418,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_306473,RMVar_hsa_circ_68132,RMVar_hsa_circ_218313,RMVar_hsa_circ_218311,RMVar_hsa_circ_334070 53406 RMVar_ID_53406 Human_SNP_ID_849889331 A-to-I Human chr3 - 51972053 51972053 51972053 TTTAGTAGAGACGGGGTTCCACCATGTTGGCCAGGGTGGTCTTGAACTCCTGACCTCAGGTGATC TTTAGTAGAGACGGGGTTCCACCATGTTGGCCTGGGTGGTCTTGAACTCCTGACCTCAGGTGATC T A PCBP4,ABHD14B,AC115284.1 Ensembl:ENSG00000090097,Ensembl:ENSG00000114779,Ensembl:ENSG00000272762 Protein coding,Protein coding,lincRNA intron,intron,intron GSE47997 K562 cells&HepG2 cells chr3:51972052..51972053 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_14885838 53407 RMVar_ID_53407 Human_SNP_ID_849924257 A-to-I Human chr3 - 49098628 49098628 49098628 GGGCCAGCCTGTGGGCCTGAGGCATACAGGCTACGTCATTGAGCTGCAGCATGTTGTCAAGGTGA GGGCCAGCCTGTGGGCCTGAGGCATACAGGCTGCGTCATTGAGCTGCAGCATGTTGTCAAGGTGA T C QARS1 Ensembl:ENSG00000172053 Protein coding exon GSE112787 293 Flip-In T-REx cells,empty vector chr3:49098627..49098628 29967493 RNA-Seq:(High) rs1396216642 Functional Loss SNV COSMIC 33..33 33 kidney papillary_renal_cell_carcinoma 3 kidney Human_RBP_ID_604096,Human_RBP_ID_18012814,Human_RBP_ID_22455436,Human_RBP_ID_25763655 Human_Splice_Rec_427324,Human_Splice_Rec_427325,Human_Splice_Rec_427338,Human_Splice_Rec_427339,Human_Splice_Rec_427358,Human_Splice_Rec_427359,Human_Splice_Rec_427404,Human_Splice_Rec_427405,Human_Splice_Rec_427456,Human_Splice_Rec_427457,Human_Splice_Rec_427502,Human_Splice_Rec_427503,Human_Splice_Rec_427520,Human_Splice_Rec_427521,Human_Splice_Rec_427566,Human_Splice_Rec_427567,Human_Splice_Rec_427575,Human_Splice_Rec_427616,Human_Splice_Rec_427617,Human_Splice_Rec_427636,Human_Splice_Rec_427637,Human_Splice_Rec_427651,Human_Splice_Rec_427690,Human_Splice_Rec_427691,Human_Splice_Rec_427704,Human_Splice_Rec_427705,Human_Splice_Rec_427710,Human_Splice_Rec_427711,Human_Splice_Rec_427744,Human_Splice_Rec_427745,Human_Splice_Rec_427756,Human_Splice_Rec_427757 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,RMVar_hsa_circ_377724 53408 RMVar_ID_53408 Human_SNP_ID_849925290 A-to-I Human chr3 + 9751800 9751800 9751800 AGGTGTGCGACTGCTGCGACAAGACCCCATCGAATGCCTTTTCTCTTTTATCTGTTCCTCCAACA AGGTGTGCGACTGCTGCGACAAGACCCCATCGGATGCCTTTTCTCTTTTATCTGTTCCTCCAACA A G OGG1 Ensembl:ENSG00000114026 Protein coding CDS GSE38233 cultured B-cells chr3:9751799..9751800 24183664 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 10 large intestine Human_Splice_Rec_390456,Human_Splice_Rec_390468,Human_Splice_Rec_390480,Human_Splice_Rec_390488,Human_Splice_Rec_390500,Human_Splice_Rec_390512,Human_Splice_Rec_390526,Human_Splice_Rec_390544,Human_Splice_Rec_390548,Human_Splice_Rec_390558,Human_Splice_Rec_390564,Human_Splice_Rec_390566,Human_Splice_Rec_390572 RMVar_hsa_circ_215690,RMVar_hsa_circ_84285,RMVar_hsa_circ_290620,RMVar_hsa_circ_292327,RMVar_hsa_circ_285060,RMVar_hsa_circ_215691,RMVar_hsa_circ_215692,RMVar_hsa_circ_215688,RMVar_hsa_circ_215689,RMVar_hsa_circ_363095 53409 RMVar_ID_53409 Human_SNP_ID_849949440 A-to-I Human chr3 - 196241465 196241465 196241465 TTAGAAACTCTATATATTTTTCTGGGCATGGTAGTTCATGCCTGTACTTTGGGAGGCTGAGGCGG TTAGAAACTCTATATATTTTTCTGGGCATGGTGGTTCATGCCTGTACTTTGGGAGGCTGAGGCGG T C PCYT1A Ensembl:ENSG00000161217 Protein coding intron GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line chr3:196241464..196241465 29129909,31158229 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue RMVar_hsa_circ_59924,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_223889 53410 RMVar_ID_53410 Human_SNP_ID_849956164 A-to-I Human chr3 - 136494156 136494156 136494156 AGCAGTCCTCCTGCCTCAGCTCCCAAGTAGCTAGGACTGCAGGCAAGCTTCACGACACCTGGCCA AGCAGTCCTCCTGCCTCAGCTCCCAAGTAGCTGGGACTGCAGGCAAGCTTCACGACACCTGGCCA T C STAG1 Ensembl:ENSG00000118007 Protein coding intron GSE100210 HepG2 cell line chr3:136494155..136494156 29129909 RNA-Seq:(High) rs1413240449 Functional Loss SNV ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 5 lung Human_RBP_ID_14635306 RMVar_hsa_circ_457,RMVar_hsa_circ_56127,RMVar_hsa_circ_373679,RMVar_hsa_circ_44526,RMVar_hsa_circ_221566,RMVar_hsa_circ_364651,RMVar_hsa_circ_309922,RMVar_hsa_circ_31195,RMVar_hsa_circ_316408,RMVar_hsa_circ_352868,RMVar_hsa_circ_363905,RMVar_hsa_circ_294705,RMVar_hsa_circ_52321,RMVar_hsa_circ_55139,RMVar_hsa_circ_74540,RMVar_hsa_circ_221583,RMVar_hsa_circ_221582,RMVar_hsa_circ_279592,RMVar_hsa_circ_47066,RMVar_hsa_circ_221592,RMVar_hsa_circ_6847,RMVar_hsa_circ_364177,RMVar_hsa_circ_346727,RMVar_hsa_circ_15347,RMVar_hsa_circ_40674,RMVar_hsa_circ_294788,RMVar_hsa_circ_221596,RMVar_hsa_circ_349971,RMVar_hsa_circ_61270,RMVar_hsa_circ_68680,RMVar_hsa_circ_221598,RMVar_hsa_circ_307030,RMVar_hsa_circ_221601,RMVar_hsa_circ_271558,RMVar_hsa_circ_221600,RMVar_hsa_circ_338771,RMVar_hsa_circ_357877,RMVar_hsa_circ_371491,RMVar_hsa_circ_50645,RMVar_hsa_circ_90420,RMVar_hsa_circ_221603,RMVar_hsa_circ_221602,RMVar_hsa_circ_221607,RMVar_hsa_circ_316964,RMVar_hsa_circ_329401,RMVar_hsa_circ_354151,RMVar_hsa_circ_221606,RMVar_hsa_circ_14145,RMVar_hsa_circ_62827,RMVar_hsa_circ_358167 53411 RMVar_ID_53411 Human_SNP_ID_850003896 A-to-I Human chr3 - 53313367 53313367 53313367 TTACCCAGGCTGGAGTGCAGTAGTGTGATCTCAGTTCACTGCAGCCTCTACCTCCCAGACTCAAG TTACCCAGGCTGGAGTGCAGTAGTGTGATCTCTGTTCACTGCAGCCTCTACCTCCCAGACTCAAG T A DCP1A Ensembl:ENSG00000272886 Protein coding intron GSE38233 cultured B-cells chr3:53313366..53313367 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 3 oesophagus RMVar_hsa_circ_320801,RMVar_hsa_circ_287095,RMVar_hsa_circ_11277,RMVar_hsa_circ_273525 53412 RMVar_ID_53412 Human_SNP_ID_850005019 A-to-I Human chr3 - 177188096 177188096 177188096 AAAACCCCGTCTCTACTAAAAATACAGAAATTAGCCGGGTGTGGTGGCATGTGCCTGTAATCCCA AAAACCCCGTCTCTACTAAAAATACAGAAATTGGCCGGGTGTGGTGGCATGTGCCTGTAATCCCA T C TBL1XR1 Ensembl:ENSG00000177565 Protein coding intron GSE100210 HepG2 cell line chr3:177188095..177188096 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_156171 RMVar_hsa_circ_106698,RMVar_hsa_circ_100512,RMVar_hsa_circ_222818,RMVar_hsa_circ_222817,RMVar_hsa_circ_101071,RMVar_hsa_circ_222848,RMVar_hsa_circ_97020,RMVar_hsa_circ_222851 53413 RMVar_ID_53413 Human_SNP_ID_850007850 A-to-I Human chr3 + 11442846 11442846 11442846 GGGAGGCTGAGATGGGAAGATTGCTAGAGCCCAGGAGTTCGAGGCTGCATTGAGCTAAGATTGTG GGGAGGCTGAGATGGGAAGATTGCTAGAGCCCTGGAGTTCGAGGCTGCATTGAGCTAAGATTGTG A T ATG7 Ensembl:ENSG00000197548 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank chr3:11442845..11442846 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 4 liver RMVar_hsa_circ_108562,RMVar_hsa_circ_215894,RMVar_hsa_circ_215904 53414 RMVar_ID_53414 Human_SNP_ID_850109436 A-to-I Human chr3 + 33011293 33011293 33011293 CACTTTTCGAGGCCAAGTTCACATAAAAACTTACATGCAAGTGTTTACAGCAGTATTATAATAAC CACTTTTCGAGGCCAAGTTCACATAAAAACTTTCATGCAAGTGTTTACAGCAGTATTATAATAAC A T - - Other Unknown GSE100210 HepG2 cell line chr3:33011292..33011293 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 4 pancreas 53415 RMVar_ID_53415 Human_SNP_ID_850114969 A-to-I Human chr3 - 114346826 114346826 114346826 TAAAAATTAACCAGGCATGGTGCTGCATGCCTATAGTTCCAGCTACTTGGGACGCTGAAATGGGA TAAAAATTAACCAGGCATGGTGCTGCATGCCTGTAGTTCCAGCTACTTGGGACGCTGAAATGGGA T C ZBTB20 Ensembl:ENSG00000181722 Protein coding intron GSE100210 HepG2 cell line chr3:114346825..114346826 29129909 RNA-Seq:(High) rs1266520925 Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 8 oesophagus 53416 RMVar_ID_53416 Human_SNP_ID_850126194 A-to-I Human chr3 - 138498515 138498515 138498515 CCTGGCTAACACGGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTAGTCGGGCGTAGTGGCA CCTGGCTAACACGGTGAAACCCCGTCTCTACTGAAAATACAAAAAATTAGTCGGGCGTAGTGGCA T C CEP70 Ensembl:ENSG00000114107 Protein coding intron GSE100210 HepG2 cell line chr3:138498514..138498515 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 5 oesophagus Human_RBP_ID_157348 RMVar_hsa_circ_221666,RMVar_hsa_circ_68372,RMVar_hsa_circ_330536,RMVar_hsa_circ_368451,RMVar_hsa_circ_353498,RMVar_hsa_circ_282162,RMVar_hsa_circ_28749,RMVar_hsa_circ_61329,RMVar_hsa_circ_221667,RMVar_hsa_circ_221668 53417 RMVar_ID_53417 Human_SNP_ID_850178085 A-to-I Human chr3 + 179745175 179745175 179745175 TCAGGCCTTCTCTGAACCAGAAAATGTTGATGATTTCTGGAGCAGTGCCCTACAAGCAAAGTCTG TCAGGCCTTCTCTGAACCAGAAAATGTTGATGCTTTCTGGAGCAGTGCCCTACAAGCAAAGTCTG A C USP13 Ensembl:ENSG00000058056 Protein coding CDS GSE100210 HepG2 cell line chr3:179745174..179745175 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_1956602,Human_RBP_ID_8236117,Human_RBP_ID_9394270,Human_RBP_ID_17703374,Human_RBP_ID_19013143,Human_RBP_ID_23987119 Human_Splice_Rec_509565,Human_Splice_Rec_509641,Human_Splice_Rec_509667 RMVar_hsa_circ_80006,RMVar_hsa_circ_51733,RMVar_hsa_circ_81799,RMVar_hsa_circ_53421,RMVar_hsa_circ_222960,RMVar_hsa_circ_222961,RMVar_hsa_circ_92857,RMVar_hsa_circ_222962,RMVar_hsa_circ_299439,RMVar_hsa_circ_38073,RMVar_hsa_circ_87232,RMVar_hsa_circ_107551,RMVar_hsa_circ_222966,RMVar_hsa_circ_91810,RMVar_hsa_circ_222968,RMVar_hsa_circ_222970,RMVar_hsa_circ_25407,RMVar_hsa_circ_222969,RMVar_hsa_circ_322261,RMVar_hsa_circ_336583,RMVar_hsa_circ_283528,RMVar_hsa_circ_50725,RMVar_hsa_circ_222971,RMVar_hsa_circ_265204,RMVar_hsa_circ_340430,RMVar_hsa_circ_315413,RMVar_hsa_circ_53063,RMVar_hsa_circ_222973 53418 RMVar_ID_53418 Human_SNP_ID_850194841 A-to-I Human chr3 - 113714408 113714408 113714408 GGCTAACACGGTGAAACCCCGTCTCTACTAAAAATACAAAAAATTGGCCGGGCGCAGTGGCAGGC GGCTAACACGGTGAAACCCCGTCTCTACTAAATATACAAAAAATTGGCCGGGCGCAGTGGCAGGC T A - - Other Unknown GSE100210 HepG2 cell line chr3:113714407..113714408 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - 53419 RMVar_ID_53419 Human_SNP_ID_850252810 A-to-I Human chr3 - 196062457 196062457 196062457 ACGATCTCGGCTCACTGCAACCTCTGTCTCCCAGATTCAAGCGATTCTCCTGCCTTAGCCTCCTG ACGATCTCGGCTCACTGCAACCTCTGTCTCCCGGATTCAAGCGATTCTCCTGCCTTAGCCTCCTG T C TFRC Ensembl:ENSG00000072274 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr3:196062456..196062457 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue RMVar_hsa_circ_67433,RMVar_hsa_circ_223845,RMVar_hsa_circ_111324,RMVar_hsa_circ_121595,RMVar_hsa_circ_128066,RMVar_hsa_circ_80284,RMVar_hsa_circ_223846,RMVar_hsa_circ_223843,RMVar_hsa_circ_223844,RMVar_hsa_circ_340292,RMVar_hsa_circ_363377,RMVar_hsa_circ_334288,RMVar_hsa_circ_308948,RMVar_hsa_circ_3131,RMVar_hsa_circ_22311,RMVar_hsa_circ_223854,RMVar_hsa_circ_65137,RMVar_hsa_circ_223853,RMVar_hsa_circ_377340,RMVar_hsa_circ_103045,RMVar_hsa_circ_340924,RMVar_hsa_circ_223855,RMVar_hsa_circ_223856,RMVar_hsa_circ_343677,RMVar_hsa_circ_367866,RMVar_hsa_circ_341777,RMVar_hsa_circ_310545,RMVar_hsa_circ_321932,RMVar_hsa_circ_59092,RMVar_hsa_circ_106356,RMVar_hsa_circ_34129,RMVar_hsa_circ_103477,RMVar_hsa_circ_223857,RMVar_hsa_circ_223859,RMVar_hsa_circ_223860,RMVar_hsa_circ_223858,RMVar_hsa_circ_223863,RMVar_hsa_circ_126589,RMVar_hsa_circ_370056,RMVar_hsa_circ_370440,RMVar_hsa_circ_223865,RMVar_hsa_circ_21161,RMVar_hsa_circ_223866,RMVar_hsa_circ_223864 53420 RMVar_ID_53420 Human_SNP_ID_850296578 A-to-I Human chr3 - 195713340 195713340 195713340 GGCTGGAGGACAGGTCAGGGAGGAGTTAGGGCAGGAGGACGGGTCAGGGAGGAGTTAGGGGAGGA GGCTGGAGGACAGGTCAGGGAGGAGTTAGGGCTGGAGGACGGGTCAGGGAGGAGTTAGGGGAGGA T A lnc-MUC4-1,lnc-MUC4-1:2,lnc-MUC4-1:3,lnc-MUC4-1:4,lnc-MUC4-1:5,lnc-MUC4-1:6,lnc-MUC4-1:7,lnc-MUC4-1:8,lnc-MUC4-1:9,lnc-MUC4-1:10,lnc-MUC4-1:11 RNACentral:URS00008B3FD5,RNACentral:URS00009AE9A5,RNACentral:URS00008C0305,RNACentral:URS00008B5DFF,RNACentral:URS00008B8BE9,RNACentral:URS00008B9F05,RNACentral:URS00008B3E40,RNACentral:URS00008BBB00,RNACentral:URS00008B8D8F,RNACentral:URS00008BC148,RNACentral:URS00008BC0B7 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,intron,intron,intron,intron,exon,exon,intron,intron,exon,intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr3:195713339..195713340 30559470 RNA-Seq:(High) rs774049789 Functional Loss SNV ICGC 33..33 33 LAML 1 - 53421 RMVar_ID_53421 Human_SNP_ID_850315340 A-to-I Human chr3 + 49984150 49984150 49984150 TCTATCTCTCCAAAAAAAATACAAAAAAAATTAGCTGGATGTGGTGGTGCATGCTTGTAGTCCCA TCTATCTCTCCAAAAAAAATACAAAAAAAATTGGCTGGATGTGGTGGTGCATGCTTGTAGTCCCA A G RBM6 Ensembl:ENSG00000004534 Protein coding intron GSE38233 cultured B-cells chr3:49984149..49984150 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_15596,RMVar_hsa_circ_90903,RMVar_hsa_circ_218306,RMVar_hsa_circ_218304,RMVar_hsa_circ_122766,RMVar_hsa_circ_368196,RMVar_hsa_circ_125334,RMVar_hsa_circ_54905,RMVar_hsa_circ_280801,RMVar_hsa_circ_368344,RMVar_hsa_circ_306069,RMVar_hsa_circ_350418,RMVar_hsa_circ_218309,RMVar_hsa_circ_68124,RMVar_hsa_circ_35798,RMVar_hsa_circ_218310,RMVar_hsa_circ_290547,RMVar_hsa_circ_306473,RMVar_hsa_circ_68132,RMVar_hsa_circ_218313,RMVar_hsa_circ_218311,RMVar_hsa_circ_218312,RMVar_hsa_circ_334070 53422 RMVar_ID_53422 Human_SNP_ID_850365898 A-to-I Human chr3 + 58156064 58156064 58156064 CACCCTCCGACGACGCCCGCCGCCTCACTGTTATGAGCCTTCAGGTGAGATGCAAGGAAGCATCC CACCCTCCGACGACGCCCGCCGCCTCACTGTTGTGAGCCTTCAGGTGAGATGCAAGGAAGCATCC A G FLNB Ensembl:ENSG00000136068 Protein coding CDS GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr3:58156063..58156064 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 11 haematopoietic and lymphoid tissue Human_Splice_Rec_445895,Human_Splice_Rec_445983,Human_Splice_Rec_446073,Human_Splice_Rec_446163,Human_Splice_Rec_446249,Human_Splice_Rec_446287,Human_Splice_Rec_446309,Human_Splice_Rec_446311 Human_miRNA_ID_228477,Human_miRNA_ID_591321 RMVar_hsa_circ_92492,RMVar_hsa_circ_219168,RMVar_hsa_circ_119463,RMVar_hsa_circ_219196,RMVar_hsa_circ_32016,RMVar_hsa_circ_81753,RMVar_hsa_circ_267721,RMVar_hsa_circ_370760,RMVar_hsa_circ_108769,RMVar_hsa_circ_7589,RMVar_hsa_circ_219231,RMVar_hsa_circ_219233,RMVar_hsa_circ_219232,RMVar_hsa_circ_20324,RMVar_hsa_circ_219252,RMVar_hsa_circ_312754,RMVar_hsa_circ_59015,RMVar_hsa_circ_93955,RMVar_hsa_circ_219253,RMVar_hsa_circ_88289,RMVar_hsa_circ_126490,RMVar_hsa_circ_219255,RMVar_hsa_circ_219258,RMVar_hsa_circ_219257,RMVar_hsa_circ_373808 53423 RMVar_ID_53423 Human_SNP_ID_850402233 A-to-I Human chr3 - 195338520 195338520 195338520 AGCGAGGAGTTTGAGACCAGACTGTGCAACACAGTGAGAACCTGTCTCTACAAAAAGTAAAAAAA AGCGAGGAGTTTGAGACCAGACTGTGCAACACTGTGAGAACCTGTCTCTACAAAAAGTAAAAAAA T A ACAP2 Ensembl:ENSG00000114331 Protein coding intron GSE100210 HepG2 cell line chr3:195338519..195338520 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 RECA 1 - 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 53424 RMVar_ID_53424 Human_SNP_ID_850409781 A-to-I Human chr3 - 14172985 14172985 14172985 AAGTTTCACAAGGAAAGAGGAAAAGAGGCTGCAGTCATCCTGGGGGTTCAGCAGATGGTCCAGCA AAGTTTCACAAGGAAAGAGGAAAAGAGGCTGCTGTCATCCTGGGGGTTCAGCAGATGGTCCAGCA T A XPC Ensembl:ENSG00000154767 Protein coding CDS GSE100210 HepG2 cell line chr3:14172984..14172985 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 2 liver Human_RBP_ID_934846,Human_RBP_ID_1633058,Human_RBP_ID_5530213,Human_RBP_ID_7130824,Human_RBP_ID_9393337,Human_RBP_ID_19009884,Human_RBP_ID_26347771,Human_RBP_ID_27821938 Human_Splice_Rec_397210,Human_Splice_Rec_397240,Human_Splice_Rec_397296 RMVar_hsa_circ_60924,RMVar_hsa_circ_364754,RMVar_hsa_circ_336902 53425 RMVar_ID_53425 Human_SNP_ID_850423121 A-to-I Human chr3 - 142490127 142490127 142490127 TTGAGCCTAGGAGTTCAAGGTTACAGTTAGCTATGATTGCACCACTGCATTCCAGCCTGAGTTAC TTGAGCCTAGGAGTTCAAGGTTACAGTTAGCTGTGATTGCACCACTGCATTCCAGCCTGAGTTAC T C ATR Ensembl:ENSG00000175054 Protein coding intron GSE38233 cultured B-cells chr3:142490126..142490127 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_80440,RMVar_hsa_circ_305477,RMVar_hsa_circ_337707,RMVar_hsa_circ_268537,RMVar_hsa_circ_346058,RMVar_hsa_circ_221941,RMVar_hsa_circ_221940,RMVar_hsa_circ_118853,RMVar_hsa_circ_116041,RMVar_hsa_circ_9512,RMVar_hsa_circ_312020,RMVar_hsa_circ_7513,RMVar_hsa_circ_221943,RMVar_hsa_circ_221944,RMVar_hsa_circ_378700,RMVar_hsa_circ_269638,RMVar_hsa_circ_370402,RMVar_hsa_circ_221945,RMVar_hsa_circ_341915,RMVar_hsa_circ_50596,RMVar_hsa_circ_120654,RMVar_hsa_circ_63219,RMVar_hsa_circ_33257,RMVar_hsa_circ_221946,RMVar_hsa_circ_221947,RMVar_hsa_circ_114937,RMVar_hsa_circ_33977,RMVar_hsa_circ_221951,RMVar_hsa_circ_221952,RMVar_hsa_circ_280654,RMVar_hsa_circ_56898,RMVar_hsa_circ_221954,RMVar_hsa_circ_221953,RMVar_hsa_circ_132,RMVar_hsa_circ_109015,RMVar_hsa_circ_107476,RMVar_hsa_circ_298007,RMVar_hsa_circ_341053,RMVar_hsa_circ_78247,RMVar_hsa_circ_221956,RMVar_hsa_circ_45461,RMVar_hsa_circ_221957,RMVar_hsa_circ_221955 53426 RMVar_ID_53426 Human_SNP_ID_850455180 A-to-I Human chr3 + 49009082 49009082 49009082 TGTTGTATTTTTAGTAGAGATGGGGCCTCACCATGTTGGCCAGGCTGGTCTCAAACTCCTGACCT TGTTGTATTTTTAGTAGAGATGGGGCCTCACCGTGTTGGCCAGGCTGGTCTCAAACTCCTGACCT A G WDR6 Ensembl:ENSG00000178252 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line chr3:49009081..49009082 24183664,29129909,31158229 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 53427 RMVar_ID_53427 Human_SNP_ID_850495315 A-to-I Human chr3 - 179397899 179397899 179397899 TGGTGAAACCCCATCTCTACTAAAAATACAAAAATTAGCCGGGCGTGGAGGTGGGCGCCTGTCAG TGGTGAAACCCCATCTCTACTAAAAATACAAAGATTAGCCGGGCGTGGAGGTGGGCGCCTGTCAG T C GNB4 Ensembl:ENSG00000114450 Protein coding 3'UTR GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line chr3:179397898..179397899 23474544,29129909 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus RMVar_hsa_circ_105486,RMVar_hsa_circ_117926,RMVar_hsa_circ_128128,RMVar_hsa_circ_110542,RMVar_hsa_circ_222912,RMVar_hsa_circ_89333,RMVar_hsa_circ_94368,RMVar_hsa_circ_222914,RMVar_hsa_circ_85129,RMVar_hsa_circ_222915,RMVar_hsa_circ_222913,RMVar_hsa_circ_222910,RMVar_hsa_circ_222911,RMVar_hsa_circ_222909 53428 RMVar_ID_53428 Human_SNP_ID_850538061 A-to-I Human chr3 + 184150448 184150448 184150448 AGCCAGTCCCTACAGCATAACAGGGTCTCCTTAGCAGCTGTATTCTGGAGTCTGGATGTTGCTCT AGCCAGTCCCTACAGCATAACAGGGTCTCCTTCGCAGCTGTATTCTGGAGTCTGGATGTTGCTCT A C - - Other Unknown GSE100210 HepG2 cell line chr3:184150447..184150448 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_596399,Human_RBP_ID_26511923 53429 RMVar_ID_53429 Human_SNP_ID_850660643 A-to-I Human chr3 - 52525275 52525275 52525275 TCCTCTCCCTAGGGAAACCTGTTTGACTTCTTACGCTTGACGGAATGGCGTGGCCCCCGCGTGCT TCCTCTCCCTAGGGAAACCTGTTTGACTTCTTGCGCTTGACGGAATGGCGTGGCCCCCGCGTGCT T C NT5DC2 Ensembl:ENSG00000168268 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector chr3:52525274..52525275 29967493 RNA-Seq:(High) rs11545651 Functional Loss SNV COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 3 brain Human_RBP_ID_70223,Human_RBP_ID_605504,Human_RBP_ID_933826,Human_RBP_ID_4749559,Human_RBP_ID_8576120,Human_RBP_ID_8875051,Human_RBP_ID_17292708,Human_RBP_ID_17404655,Human_RBP_ID_17521430,Human_RBP_ID_19010581,Human_RBP_ID_27320988 Human_Splice_Rec_438688,Human_Splice_Rec_438689,Human_Splice_Rec_438695,Human_Splice_Rec_438720,Human_Splice_Rec_438721,Human_Splice_Rec_438746,Human_Splice_Rec_438747,Human_Splice_Rec_438753,Human_Splice_Rec_438776,Human_Splice_Rec_438777,Human_Splice_Rec_438800,Human_Splice_Rec_438801,Human_Splice_Rec_438810,Human_Splice_Rec_438811,Human_Splice_Rec_438822,Human_Splice_Rec_438823 Human_miRNA_ID_1337337,Human_miRNA_ID_1354203 RMVar_hsa_circ_57122 53430 RMVar_ID_53430 Human_SNP_ID_850668379 A-to-I Human chr3 - 196078956 196078956 196078956 CAGCCTGGCCAACGTGGTAAAATCCCGTCTCTACTAAAAATACAAAAATTAGCTGGGCATGGTGG CAGCCTGGCCAACGTGGTAAAATCCCGTCTCTGCTAAAAATACAAAAATTAGCTGGGCATGGTGG T C TFRC Ensembl:ENSG00000072274 Protein coding intron GSE38233 cultured B-cells chr3:196078955..196078956 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 53431 RMVar_ID_53431 Human_SNP_ID_850679333 A-to-I Human chr3 + 122614771 122614771 122614771 AGAAACATGGACTGGTGCAGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCTGAGGCAGGG AGAAACATGGACTGGTGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGG A G PARP15 Ensembl:ENSG00000173200 Protein coding intron GSE38233 cultured B-cells chr3:122614770..122614771 24183664 RNA-Seq:(High) rs995554663 Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 2 prostate RMVar_hsa_circ_71462,RMVar_hsa_circ_356477,RMVar_hsa_circ_362185,RMVar_hsa_circ_220667 53432 RMVar_ID_53432 Human_SNP_ID_850684038 A-to-I Human chr3 - 125118840 125118840 125118840 CTCTTGGGTTTTGCAGGTGGTTTCTGTACATCATCTTCGTCTTCCTCCTGGGCGCCATCTGCACT CTCTTGGGTTTTGCAGGTGGTTTCTGTACATCGTCTTCGTCTTCCTCCTGGGCGCCATCTGCACT T C SLC12A8 Ensembl:ENSG00000221955 Protein coding CDS GSE100210 HepG2 cell line chr3:125118839..125118840 29129909 RNA-Seq:(High) rs621383 Functional Loss SNV ICGC 33..33 33 COCA 5 - Human_Splice_Rec_476614,Human_Splice_Rec_476615,Human_Splice_Rec_476638,Human_Splice_Rec_476639,Human_Splice_Rec_476662,Human_Splice_Rec_476663,Human_Splice_Rec_476678,Human_Splice_Rec_476679,Human_Splice_Rec_476698,Human_Splice_Rec_476699,Human_Splice_Rec_476714,Human_Splice_Rec_476715,Human_Splice_Rec_476730,Human_Splice_Rec_476731,Human_Splice_Rec_476749,Human_Splice_Rec_476758,Human_Splice_Rec_476759,Human_Splice_Rec_476768,Human_Splice_Rec_476769,Human_Splice_Rec_476786,Human_Splice_Rec_476787 RMVar_hsa_circ_79250,RMVar_hsa_circ_83609,RMVar_hsa_circ_220857,RMVar_hsa_circ_220858,RMVar_hsa_circ_295023,RMVar_hsa_circ_220860,RMVar_hsa_circ_296013,RMVar_hsa_circ_322494 53433 RMVar_ID_53433 Human_SNP_ID_820860939 A-to-I Human chr14 - 81916672 81916672 81916672 ATTGCAATTGTTATAATAGGATTCAAACCTCTACTCCAAGGAAGGTCCCCCACTGACTTTGGCAT ATTGCAATTGTTATAATAGGATTCAAACCTCTGCTCCAAGGAAGGTCCCCCACTGACTTTGGCAT T C - - Other Unknown GSE100210 HepG2 cell line chr14:81916671..81916672 29129909 RNA-Seq:(High) rs878856575 Functional Loss SNV ICGC 33..33 33 LAML 2 - 53434 RMVar_ID_53434 Human_SNP_ID_820864461 A-to-I Human chr14 - 89943529 89943529 89943529 ATCTTGAAGAACTGAAATTGGCGGGGTGTGGTAGCTCACGCCTGTAGTCCCATGCAATTTGGGAG ATCTTGAAGAACTGAAATTGGCGGGGTGTGGTTGCTCACGCCTGTAGTCCCATGCAATTTGGGAG T A AL137230.3,EFCAB11 Ensembl:ENSG00000259053,Ensembl:ENSG00000140025 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line chr14:89943528..89943529 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - RMVar_hsa_circ_351959 53435 RMVar_ID_53435 Human_SNP_ID_820874555 A-to-I Human chr14 - 21460502 21460502 21460502 TGGCTCACTGCAACCTCCACTTTCCAGGTTCAAGCAGTTCTCCTGCCTCAACCTCCCGAGTAGCT TGGCTCACTGCAACCTCCACTTTCCAGGTTCAGGCAGTTCTCCTGCCTCAACCTCCCGAGTAGCT T C RAB2B Ensembl:ENSG00000129472 Protein coding 3'UTR GSE100210 HepG2 cell line chr14:21460501..21460502 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_105125,RMVar_hsa_circ_120911,RMVar_hsa_circ_165206,RMVar_hsa_circ_82966,RMVar_hsa_circ_165207,RMVar_hsa_circ_165205 53436 RMVar_ID_53436 Human_SNP_ID_820917580 A-to-I Human chr14 + 50051007 50051007 50051007 CAAAACAGTCTGTGTCTTTTCTGGTTTTGCAGAAAATCCTGGAGTCTGAAGAAAAAGAGGATCCC CAAAACAGTCTGTGTCTTTTCTGGTTTTGCAGGAAATCCTGGAGTCTGAAGAAAAAGAGGATCCC A G PDLIM1P1 Ensembl:ENSG00000270788 Pseudogene exon GSE100210 HepG2 cell line chr14:50051006..50051007 29129909 RNA-Seq:(High) rs1390369048 Functional Loss SNV ICGC 33..33 33 LAML 2 - 53437 RMVar_ID_53437 Human_SNP_ID_820922023 A-to-I Human chr14 + 55061011 55061011 55061011 AAATTTTTAAAATTTTAAGAAATTTGCTGGGCATGATGGCACACACCTGTAGTACCGGCTATTAG AAATTTTTAAAATTTTAAGAAATTTGCTGGGCGTGATGGCACACACCTGTAGTACCGGCTATTAG A G MAPK1IP1L Ensembl:ENSG00000168175 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr14:55061010..55061011 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_6359423,Human_RBP_ID_12357950 RMVar_hsa_circ_112430,RMVar_hsa_circ_166826 53438 RMVar_ID_53438 Human_SNP_ID_820945809 A-to-I Human chr14 - 31397780 31397780 31397780 GTGGTGAACACCTGTAGTTCTAGCCCCTCGGAAGACTGAGGCAGGAGGATCACTTGAGCCCAGGA GTGGTGAACACCTGTAGTTCTAGCCCCTCGGAGGACTGAGGCAGGAGGATCACTTGAGCCCAGGA T C AL139353.1,HEATR5A Ensembl:ENSG00000203546,Ensembl:ENSG00000129493 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line chr14:31397779..31397780 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_119850,RMVar_hsa_circ_165681,RMVar_hsa_circ_99941,RMVar_hsa_circ_165686,RMVar_hsa_circ_111300,RMVar_hsa_circ_21928,RMVar_hsa_circ_106760,RMVar_hsa_circ_165743,RMVar_hsa_circ_86572,RMVar_hsa_circ_165744,RMVar_hsa_circ_165750,RMVar_hsa_circ_373676,RMVar_hsa_circ_165755,RMVar_hsa_circ_55635,RMVar_hsa_circ_33475,RMVar_hsa_circ_43127,RMVar_hsa_circ_61300,RMVar_hsa_circ_360502,RMVar_hsa_circ_374470,RMVar_hsa_circ_321299,RMVar_hsa_circ_165769,RMVar_hsa_circ_26463 53439 RMVar_ID_53439 Human_SNP_ID_820948927 A-to-I Human chr14 - 92059690 92059690 92059690 CCTCAGCCTCCCAAGTACCTGGGATTACAGGCACCTGCCACTACACCTGGCGAATATTTGTTTTT CCTCAGCCTCCCAAGTACCTGGGATTACAGGCCCCTGCCACTACACCTGGCGAATATTTGTTTTT T G ATXN3 Ensembl:ENSG00000066427 Protein coding intron GSE100210 HepG2 cell line chr14:92059689..92059690 29129909 RNA-Seq:(High) rs969266308 Functional Loss SNV ICGC 33..33 33 LICA 1 - 53440 RMVar_ID_53440 Human_SNP_ID_820989906 A-to-I Human chr14 + 64451224 64451224 64451224 TTATTTTTCTTGTAGTGACTGGGTCTCCCTATATTGCTCAGGCTGGTCTCGAACTCCTGGGTTCA TTATTTTTCTTGTAGTGACTGGGTCTCCCTATGTTGCTCAGGCTGGTCTCGAACTCCTGGGTTCA A G MTHFD1 Ensembl:ENSG00000100714 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr14:64451223..64451224 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_73389,RMVar_hsa_circ_88169,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_373779,RMVar_hsa_circ_167272,RMVar_hsa_circ_355605,RMVar_hsa_circ_353213,RMVar_hsa_circ_167279,RMVar_hsa_circ_293785,RMVar_hsa_circ_98797,RMVar_hsa_circ_167284,RMVar_hsa_circ_346822,RMVar_hsa_circ_167287 53441 RMVar_ID_53441 Human_SNP_ID_821027236 A-to-I Human chr14 - 21162666 21162666 21162666 GTGGTTTTGGAATCATAATACCAGAGGATGCCATGACCCGGCTGTTGGTGCCCGGGTTCCCTCCC GTGGTTTTGGAATCATAATACCAGAGGATGCCGTGACCCGGCTGTTGGTGCCCGGGTTCCCTCCC T C - - Other Unknown GSE100210 HepG2 cell line chr14:21162665..21162666 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 1 - 53442 RMVar_ID_53442 Human_SNP_ID_821063161 A-to-I Human chr14 + 44120722 44120722 44120722 AGATCCCAGATCATCATCTGGGGAGGCTGAACACTTCACCCCATGCAGGTGAGACTCTCTGGCAG AGATCCCAGATCATCATCTGGGGAGGCTGAACGCTTCACCCCATGCAGGTGAGACTCTCTGGCAG A G - - Other Unknown GSE100210 HepG2 cell line chr14:44120721..44120722 29129909 RNA-Seq:(High) rs878962870 Functional Loss SNV ICGC 33..33 33 LAML 2 - 53443 RMVar_ID_53443 Human_SNP_ID_821075176 A-to-I Human chr14 + 102879432 102879432 102879432 GGTGCATGCTACCATGCCTGGCTAATTTTTGTATTTTTTGTAGAGACAGGGTCTTGCCATGTTGC GGTGCATGCTACCATGCCTGGCTAATTTTTGTGTTTTTTGTAGAGACAGGGTCTTGCCATGTTGC A G TRAF3 Ensembl:ENSG00000131323 Protein coding intron GSE100210 HepG2 cell line chr14:102879431..102879432 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_2753,RMVar_hsa_circ_169430,RMVar_hsa_circ_95533,RMVar_hsa_circ_273169,RMVar_hsa_circ_169428,RMVar_hsa_circ_309358,RMVar_hsa_circ_318210,RMVar_hsa_circ_23381,RMVar_hsa_circ_169431,RMVar_hsa_circ_28884,RMVar_hsa_circ_297681,RMVar_hsa_circ_336338,RMVar_hsa_circ_169429,RMVar_hsa_circ_297188,RMVar_hsa_circ_273716,RMVar_hsa_circ_169435,RMVar_hsa_circ_169437,RMVar_hsa_circ_169438,RMVar_hsa_circ_169436,RMVar_hsa_circ_64275,RMVar_hsa_circ_169439,RMVar_hsa_circ_100298,RMVar_hsa_circ_9633 53444 RMVar_ID_53444 Human_SNP_ID_821089253 A-to-I Human chr14 - 50050684 50050684 50050684 TTCCTATGTGCAGGACCTCCTGGGGTTCAGAGACTAAATTCATCTTGTATGGACGACACTTCTCT TTCCTATGTGCAGGACCTCCTGGGGTTCAGAGGCTAAATTCATCTTGTATGGACGACACTTCTCT T C LINC01588 Ensembl:ENSG00000214900 lincRNA intron GSE100210 HepG2 cell line chr14:50050683..50050684 29129909 RNA-Seq:(High) rs1225914034 Functional Loss SNV ICGC 33..33 33 LAML 1 - RMVar_hsa_circ_166404,RMVar_hsa_circ_64407,RMVar_hsa_circ_329079,RMVar_hsa_circ_307436,RMVar_hsa_circ_312986,RMVar_hsa_circ_166405 53445 RMVar_ID_53445 Human_SNP_ID_821212516 A-to-I Human chr14 - 50246084 50246084 50246084 AGTTTCACTCTTGTTGCCCAGGCTTGAGTGCAATGGTACGATCTTGGCTCACTGCAACCTCTGCC AGTTTCACTCTTGTTGCCCAGGCTTGAGTGCATTGGTACGATCTTGGCTCACTGCAACCTCTGCC T A L2HGDH Ensembl:ENSG00000087299 Protein coding intron GSE38233 cultured B-cells chr14:50246083..50246084 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_Splice_Rec_1512442 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 53446 RMVar_ID_53446 Human_SNP_ID_821269762 A-to-I Human chr14 - 63601697 63601697 63601697 TATGGGAGAAGAACTTTATCTCCAACTTTCACACGAACTGGTTGAATCTCTCCACCCTTTCCTTT TATGGGAGAAGAACTTTATCTCCAACTTTCACGCGAACTGGTTGAATCTCTCCACCCTTTCCTTT T C WDR89 Ensembl:ENSG00000140006 Protein coding intron GSE100210 HepG2 cell line chr14:63601696..63601697 29129909 RNA-Seq:(High) rs546819518 Functional Loss SNV ICGC,COSMIC 33..33 33 pancreas ductal_carcinoma,LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 8 pancreas,haematopoietic and lymphoid tissue RMVar_hsa_circ_120390,RMVar_hsa_circ_167171 53447 RMVar_ID_53447 Human_SNP_ID_821291792 A-to-I Human chr14 + 73147125 73147125 73147125 CTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGATGCGCGCCACCACACCCGGCTAATTTTT CTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTGCAGATGCGCGCCACCACACCCGGCTAATTTTT A G PSEN1 Ensembl:ENSG00000080815 Protein coding intron GSE38233 cultured B-cells chr14:73147124..73147125 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 53448 RMVar_ID_53448 Human_SNP_ID_821300697 A-to-I Human chr14 - 28264622 28264622 28264622 GCTGGAACACTGCCCCCTTTCCCATTATTGCTAAAGTGCAATTCTACCCAGGAGCCCTGCAGGCT GCTGGAACACTGCCCCCTTTCCCATTATTGCTGAAGTGCAATTCTACCCAGGAGCCCTGCAGGCT T C - - Other Unknown GSE100210 HepG2 cell line chr14:28264621..28264622 29129909 RNA-Seq:(High) rs1270768105 Functional Loss SNV TCGA,ICGC 33..33 33 CESC 2 - 53449 RMVar_ID_53449 Human_SNP_ID_821315235 A-to-I Human chr14 + 103435835 103435835 103435835 GGAATTCCTGGGCTCAAGTATCTTTCCACCTCAGCCTCCTGAGGTAGCTGGGACTATAGGCGCGC GGAATTCCTGGGCTCAAGTATCTTTCCACCTCTGCCTCCTGAGGTAGCTGGGACTATAGGCGCGC A T MARK3 Ensembl:ENSG00000075413 Protein coding intron GSE38233 cultured B-cells chr14:103435834..103435835 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_6327128,Human_RBP_ID_9757970,Human_RBP_ID_12280478,Human_RBP_ID_25124716 RMVar_hsa_circ_169502,RMVar_hsa_circ_169508,RMVar_hsa_circ_306212,RMVar_hsa_circ_109771,RMVar_hsa_circ_169507,RMVar_hsa_circ_169510,RMVar_hsa_circ_284483,RMVar_hsa_circ_328268,RMVar_hsa_circ_343824,RMVar_hsa_circ_312730,RMVar_hsa_circ_169511,RMVar_hsa_circ_169509 53450 RMVar_ID_53450 Human_SNP_ID_821370127 A-to-I Human chr14 + 31093675 31093675 31093675 CACCATGTTGGCCAGGCTGTCTCAAACTCCTGACCTCAGGTGATCTGCCTGCCTCAGCCTCCCAG CACCATGTTGGCCAGGCTGTCTCAAACTCCTGCCCTCAGGTGATCTGCCTGCCTCAGCCTCCCAG A C AP4S1 Ensembl:ENSG00000100478 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells chr14:31093674..31093675 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 53451 RMVar_ID_53451 Human_SNP_ID_821379962 A-to-I Human chr14 - 21162684 21162684 21162684 GCTTATCTGATGGTTTTGGTGGTTTTGGAATCATAATACCAGAGGATGCCATGACCCGGCTGTTG GCTTATCTGATGGTTTTGGTGGTTTTGGAATCGTAATACCAGAGGATGCCATGACCCGGCTGTTG T C - - Other Unknown GSE100210 HepG2 cell line chr14:21162683..21162684 29129909 RNA-Seq:(High) rs1248868050 Functional Loss SNV ICGC 33..33 33 LAML 1 - 53452 RMVar_ID_53452 Human_SNP_ID_821440316 A-to-I Human chr14 - 100353802 100353802 100353802 TCCAGATGACGGATGACGAGAAGTATCTGTGGAAGGACCTGACCCTGGACCAGGCCTATAGCTAT TCCAGATGACGGATGACGAGAAGTATCTGTGGCAGGACCTGACCCTGGACCAGGCCTATAGCTAT T G WARS1 Ensembl:ENSG00000140105 Protein coding CDS GSE100210 HepG2 cell line chr14:100353801..100353802 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma 6 haematopoietic and lymphoid tissue Human_RBP_ID_1487638,Human_RBP_ID_1814243,Human_RBP_ID_6323148,Human_RBP_ID_8398527,Human_RBP_ID_8798190,Human_RBP_ID_12267157,Human_RBP_ID_17478120,Human_RBP_ID_18644713,Human_RBP_ID_22438564,Human_RBP_ID_22926238,Human_RBP_ID_24530806 Human_Splice_Rec_1553012,Human_Splice_Rec_1553030,Human_Splice_Rec_1553050,Human_Splice_Rec_1553068,Human_Splice_Rec_1553090,Human_Splice_Rec_1553110,Human_Splice_Rec_1553144,Human_Splice_Rec_1553156,Human_Splice_Rec_1553164,Human_Splice_Rec_1553178,Human_Splice_Rec_1553190,Human_Splice_Rec_1553198 RMVar_hsa_circ_3583,RMVar_hsa_circ_92847,RMVar_hsa_circ_108099,RMVar_hsa_circ_169031,RMVar_hsa_circ_82436,RMVar_hsa_circ_91764,RMVar_hsa_circ_169033,RMVar_hsa_circ_169034,RMVar_hsa_circ_169032,RMVar_hsa_circ_362448,RMVar_hsa_circ_53910,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_169040,RMVar_hsa_circ_270155,RMVar_hsa_circ_288368,RMVar_hsa_circ_334780,RMVar_hsa_circ_169041 53453 RMVar_ID_53453 Human_SNP_ID_821443441 A-to-I Human chr14 - 73278939 73278939 73278939 TGGGTGGATCACGAGGTCAGGAGATGGAGACCATCCTGGCCAACATGGTGAAACCATCTCTACTA TGGGTGGATCACGAGGTCAGGAGATGGAGACCGTCCTGGCCAACATGGTGAAACCATCTCTACTA T C NUMB Ensembl:ENSG00000133961 Protein coding intron GSE38233 cultured B-cells chr14:73278938..73278939 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 53454 RMVar_ID_53454 Human_SNP_ID_821481845 A-to-I Human chr14 - 68912221 68912221 68912221 TGTTTCTGTAGAAATCGTGGATGGGAATGTGAAGATGACCCTGGGCATGATCTGGACCATCATCC TGTTTCTGTAGAAATCGTGGATGGGAATGTGACGATGACCCTGGGCATGATCTGGACCATCATCC T G ACTN1 Ensembl:ENSG00000072110 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector chr14:68912220..68912221 29967493 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 stomach intestinal_adenocarcinoma 5 stomach Human_RBP_ID_881968,Human_RBP_ID_1823239,Human_RBP_ID_5563379,Human_RBP_ID_9282626,Human_RBP_ID_18469430 Human_Splice_Rec_1529264,Human_Splice_Rec_1529265,Human_Splice_Rec_1529324,Human_Splice_Rec_1529325,Human_Splice_Rec_1529366,Human_Splice_Rec_1529367,Human_Splice_Rec_1529406,Human_Splice_Rec_1529407,Human_Splice_Rec_1529454,Human_Splice_Rec_1529455,Human_Splice_Rec_1529520,Human_Splice_Rec_1529521,Human_Splice_Rec_1529538,Human_Splice_Rec_1529539,Human_Splice_Rec_1529550,Human_Splice_Rec_1529551,Human_Splice_Rec_1529566,Human_Splice_Rec_1529567,Human_Splice_Rec_1529580,Human_Splice_Rec_1529581,Human_Splice_Rec_1529592,Human_Splice_Rec_1529593,Human_Splice_Rec_1529600,Human_Splice_Rec_1529601 RMVar_hsa_circ_125579,RMVar_hsa_circ_29679,RMVar_hsa_circ_167479,RMVar_hsa_circ_114397,RMVar_hsa_circ_167484,RMVar_hsa_circ_318953,RMVar_hsa_circ_332841,RMVar_hsa_circ_315130,RMVar_hsa_circ_29360,RMVar_hsa_circ_167491,RMVar_hsa_circ_52649,RMVar_hsa_circ_24242,RMVar_hsa_circ_9256,RMVar_hsa_circ_338069,RMVar_hsa_circ_276656,RMVar_hsa_circ_167492 53455 RMVar_ID_53455 Human_SNP_ID_821511906 A-to-I Human chr14 - 50310886 50310886 50310886 GAAGAGGCTAATAATTAAATGTTGATGTTCTAAAAGTTGACTCTGGCTGCTGCGTGTTGGTGGAT GAAGAGGCTAATAATTAAATGTTGATGTTCTAGAAGTTGACTCTGGCTGCTGCGTGTTGGTGGAT T C L2HGDH Ensembl:ENSG00000087299 Protein coding intron GSE100210 HepG2 cell line chr14:50310885..50310886 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_3450770 53456 RMVar_ID_53456 Human_SNP_ID_821512443 A-to-I Human chr14 - 73730141 73730141 73730141 TTTGCTGACTTCTGCCCTAGAGGAGATGATAAAAAGGGCTTTTGGACCTGCTCCTTTTTTCAGGC TTTGCTGACTTCTGCCCTAGAGGAGATGATAAGAAGGGCTTTTGGACCTGCTCCTTTTTTCAGGC T C MIDEAS Ensembl:ENSG00000156030 Protein coding intron GSE38233 cultured B-cells chr14:73730140..73730141 24183664 RNA-Seq:(High) rs6574140 Functional Loss SNV ICGC 33..33 33 COCA 5 - Human_Splice_Rec_1534108,Human_Splice_Rec_1534109 Clinvar_Rec_51,Clinvar_Rec_52,Clinvar_Rec_53,Clinvar_Rec_54 GWAS_ID_1174,GWAS_ID_1175,GWAS_ID_1176,GWAS_ID_1177,GWAS_ID_1178,GWAS_ID_1179,GWAS_ID_1180,GWAS_ID_1181,GWAS_ID_1182 RMVar_hsa_circ_338810,RMVar_hsa_circ_351975 53457 RMVar_ID_53457 Human_SNP_ID_821534610 A-to-I Human chr14 - 22973028 22973028 22973028 TTGGCCTCCCAAAGTGCTGGGATTATAGGCGTAAGCCACTGTGTCTGGCCTAGTGTATGATTATG TTGGCCTCCCAAAGTGCTGGGATTATAGGCGTGAGCCACTGTGTCTGGCCTAGTGTATGATTATG T C AL132780.3,AJUBA Ensembl:ENSG00000259132,Ensembl:ENSG00000129474 Protein coding,Protein coding intron,3'UTR GSE100210;GSE99789 HepG2 cell line;esophageal squamous carcinoma cells,EC109 chr14:22973027..22973028 29129909,29796672 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine 53458 RMVar_ID_53458 Human_SNP_ID_821558964 A-to-I Human chr14 - 21460342 21460342 21460342 GACCTCGTGATCCGCCCACCTTGGCCTCCCAAAGTGCTGGATTACAGGTGTGAGCCACCGTGCCT GACCTCGTGATCCGCCCACCTTGGCCTCCCAAGGTGCTGGATTACAGGTGTGAGCCACCGTGCCT T C RAB2B Ensembl:ENSG00000129472 Protein coding 3'UTR GSE38233;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;Bronchiolar epithelium,BERP35T4 cell line chr14:21460341..21460342 24183664,31158229 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue Human_RBP_ID_26431557 RMVar_hsa_circ_105125,RMVar_hsa_circ_120911,RMVar_hsa_circ_165206,RMVar_hsa_circ_82966,RMVar_hsa_circ_165207,RMVar_hsa_circ_165205 53459 RMVar_ID_53459 Human_SNP_ID_821569576 A-to-I Human chr14 - 20270764 20270764 20270764 GCTGGATATGGGACATGGAGTCAAAGGAGATTATTTTGGAGCTTTAAGAGTTGATGACTCCTCTG GCTGGATATGGGACATGGAGTCAAAGGAGATTGTTTTGGAGCTTTAAGAGTTGATGACTCCTCTG T C TTC5 Ensembl:ENSG00000136319 Protein coding intron GSE100210 HepG2 cell line chr14:20270763..20270764 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BOCA 1 - 53460 RMVar_ID_53460 Human_SNP_ID_821590467 A-to-I Human chr14 + 52612665 52612665 52612665 CTTACTGTAACCTCAAACTCCTGGGCTTATGTAATTCTCCTACCTCAGCCTCCCAAGTAGCTAGA CTTACTGTAACCTCAAACTCCTGGGCTTATGTGATTCTCCTACCTCAGCCTCCCAAGTAGCTAGA A G GPR137C Ensembl:ENSG00000180998 Protein coding intron GSE100210 HepG2 cell line chr14:52612665..52612666 29129909 RNA-Seq:(High) rs993432513 Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_294060,RMVar_hsa_circ_166694 53461 RMVar_ID_53461 Human_SNP_ID_821591608 A-to-I Human chr14 - 22969643 22969643 22969643 CCACTTTGGCCTCCTAAGTCACTGGGATTACAAGCATGAGCTTCTGTGCCCAGCTCCTGACCCTT CCACTTTGGCCTCCTAAGTCACTGGGATTACAGGCATGAGCTTCTGTGCCCAGCTCCTGACCCTT T C AL132780.3 Ensembl:ENSG00000259132 Protein coding intron GSE100210 HepG2 cell line chr14:22969642..22969643 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_17562783 53462 RMVar_ID_53462 Human_SNP_ID_821610055 A-to-I Human chr14 + 91124644 91124644 91124644 ACTCTGATTCTGTGGTTAATCAGAAACAAATCAGCCTGTTTCATAGAAGCCTTTGTTGTTTGTTC ACTCTGATTCTGTGGTTAATCAGAAACAAATCGGCCTGTTTCATAGAAGCCTTTGTTGTTTGTTC A G DGLUCY Ensembl:ENSG00000133943 Protein coding intron GSE38233 cultured B-cells chr14:91124643..91124644 24183664 RNA-Seq:(High) rs4900070 Functional Loss SNV ICGC 33..33 33 ESCA 1 - GWAS_ID_292,GWAS_ID_293,GWAS_ID_294,GWAS_ID_295,GWAS_ID_296,GWAS_ID_297,GWAS_ID_298,GWAS_ID_299,GWAS_ID_300,GWAS_ID_301,GWAS_ID_302,GWAS_ID_303,GWAS_ID_304,GWAS_ID_305,GWAS_ID_306,GWAS_ID_307,GWAS_ID_308,GWAS_ID_309 53463 RMVar_ID_53463 Human_SNP_ID_821611812 A-to-I Human chr14 + 39325292 39325292 39325292 AGAATAATAAGCTTTTGTTTTCTGGACAATATAATTTTGAGAAGACCCCCCTTTTCCCTCTCAAT AGAATAATAAGCTTTTGTTTTCTGGACAATATGATTTTGAGAAGACCCCCCTTTTCCCTCTCAAT A G MIA2 Ensembl:ENSG00000150527 Protein coding intron GSE38233 cultured B-cells chr14:39325291..39325292 24183664 RNA-Seq:(High) rs12897272 Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_55578,RMVar_hsa_circ_357844,RMVar_hsa_circ_279700,RMVar_hsa_circ_284519,RMVar_hsa_circ_83225,RMVar_hsa_circ_166126,RMVar_hsa_circ_166127,RMVar_hsa_circ_13978,RMVar_hsa_circ_166132,RMVar_hsa_circ_334404,RMVar_hsa_circ_345510,RMVar_hsa_circ_166134,RMVar_hsa_circ_62818,RMVar_hsa_circ_17846,RMVar_hsa_circ_66339,RMVar_hsa_circ_93576,RMVar_hsa_circ_166135,RMVar_hsa_circ_358623,RMVar_hsa_circ_55553,RMVar_hsa_circ_302859,RMVar_hsa_circ_33419,RMVar_hsa_circ_290726,RMVar_hsa_circ_166136,RMVar_hsa_circ_289144,RMVar_hsa_circ_308040,RMVar_hsa_circ_166137,RMVar_hsa_circ_344812,RMVar_hsa_circ_166138,RMVar_hsa_circ_365935,RMVar_hsa_circ_322673,RMVar_hsa_circ_363396 53464 RMVar_ID_53464 Human_SNP_ID_821622134 A-to-I Human chr14 - 28264614 28264614 28264614 ACTGCCCCCTTTCCCATTATTGCTAAAGTGCAATTCTACCCAGGAGCCCTGCAGGCTCTCCTCCT ACTGCCCCCTTTCCCATTATTGCTAAAGTGCAGTTCTACCCAGGAGCCCTGCAGGCTCTCCTCCT T C - - Other Unknown GSE100210 HepG2 cell line chr14:28264613..28264614 29129909 RNA-Seq:(High) rs1198088670 Functional Loss SNV ICGC 33..33 33 LAML 1 - 53465 RMVar_ID_53465 Human_SNP_ID_821666068 A-to-I Human chr14 - 50742273 50742273 50742273 CCAGGTAGTTGGGACTACAGGCACACGCCACCACACTCAGCTTTTTATTTTTGGTAGAGATGGGG CCAGGTAGTTGGGACTACAGGCACACGCCACCCCACTCAGCTTTTTATTTTTGGTAGAGATGGGG T G NIN Ensembl:ENSG00000100503 Protein coding intron GSE47997 K562 cells&HepG2 cells chr14:50742272..50742273 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_6516,RMVar_hsa_circ_166555,RMVar_hsa_circ_301170,RMVar_hsa_circ_303676,RMVar_hsa_circ_5197,RMVar_hsa_circ_166557,RMVar_hsa_circ_35034,RMVar_hsa_circ_314741,RMVar_hsa_circ_166556,RMVar_hsa_circ_324957,RMVar_hsa_circ_166558,RMVar_hsa_circ_324799,RMVar_hsa_circ_7821,RMVar_hsa_circ_49435,RMVar_hsa_circ_328480,RMVar_hsa_circ_283013,RMVar_hsa_circ_322869,RMVar_hsa_circ_13864,RMVar_hsa_circ_166562,RMVar_hsa_circ_166563,RMVar_hsa_circ_166564,RMVar_hsa_circ_166561 53466 RMVar_ID_53466 Human_SNP_ID_821679815 A-to-I Human chr14 + 39177879 39177879 39177879 GCGAATATTTGGCTTGTTGATGGGTACCCTTCAAAAATTTAAACAAGAATCCACTGTTGCTACTG GCGAATATTTGGCTTGTTGATGGGTACCCTTCGAAAATTTAAACAAGAATCCACTGTTGCTACTG A G PNN Ensembl:ENSG00000100941 Protein coding CDS GSE100210 HepG2 cell line chr14:39177879..39177880 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 bile_duct adenocarcinoma,biliary_tract adenocarcinoma 2 biliary tract,gallbladder Human_RBP_ID_39515,Human_RBP_ID_883386,Human_RBP_ID_998346,Human_RBP_ID_1818932,Human_RBP_ID_5566132,Human_RBP_ID_8076599,Human_RBP_ID_8250169,Human_RBP_ID_8794416,Human_RBP_ID_9370044,Human_RBP_ID_9766257,Human_RBP_ID_12329649,Human_RBP_ID_16996845,Human_RBP_ID_17687171,Human_RBP_ID_17848354,Human_RBP_ID_18528320,Human_RBP_ID_18650397,Human_RBP_ID_22577267,Human_RBP_ID_23271853,Human_RBP_ID_25097540,Human_RBP_ID_26624769,Human_RBP_ID_27644524 Human_Splice_Rec_1509346,Human_Splice_Rec_1509347,Human_Splice_Rec_1509364,Human_Splice_Rec_1509365 RMVar_hsa_circ_29510,RMVar_hsa_circ_166119,RMVar_hsa_circ_278906,RMVar_hsa_circ_124902,RMVar_hsa_circ_166121,RMVar_hsa_circ_166120,RMVar_hsa_circ_352048 53467 RMVar_ID_53467 Human_SNP_ID_821707317 A-to-I Human chr14 - 44861460 44861460 44861460 GCTGGGATGATGGATGTCCATTATAGTGAAGAAGTTTTGCTGGAGTTGCTAGAACAATGTGTGGA GCTGGGATGATGGATGTCCATTATAGTGAAGACGTTTTGCTGGAGTTGCTAGAACAATGTGTGGA T G DOCK11P1 Ensembl:ENSG00000259000 Pseudogene exon GSE100210 HepG2 cell line chr14:44861459..44861460 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 2 - Human_RBP_ID_5563796 53468 RMVar_ID_53468 Human_SNP_ID_821707331 A-to-I Human chr14 - 44861460 44861460 44861460 GCTGGGATGATGGATGTCCATTATAGTGAAGAAGTTTTGCTGGAGTTGCTAGAACAATGTGTGGA GCTGGGATGATGGATGTCCATTATAGTGAAGAGGTTTTGCTGGAGTTGCTAGAACAATGTGTGGA T C DOCK11P1 Ensembl:ENSG00000259000 Pseudogene exon GSE100210 HepG2 cell line chr14:44861459..44861460 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_5563796 53469 RMVar_ID_53469 Human_SNP_ID_821708928 A-to-I Human chr14 - 71330595 71330595 71330595 GCCCCAAACCATCACACTGAAGAAGCCTCCTGAAGCTCAGTTGGGATTTAACATCTGAGGAGGAA GCCCCAAACCATCACACTGAAGAAGCCTCCTGGAGCTCAGTTGGGATTTAACATCTGAGGAGGAA T C AC005476.1 Ensembl:ENSG00000259079 Pseudogene exon GSE100210 HepG2 cell line chr14:71330594..71330595 29129909 RNA-Seq:(High) rs878905179 Functional Loss SNV ICGC 33..33 33 LAML 1 - 53470 RMVar_ID_53470 Human_SNP_ID_821718035 A-to-I Human chr14 - 21460331 21460331 21460331 CCGCCCACCTTGGCCTCCCAAAGTGCTGGATTACAGGTGTGAGCCACCGTGCCTGGCCTAAATAA CCGCCCACCTTGGCCTCCCAAAGTGCTGGATTGCAGGTGTGAGCCACCGTGCCTGGCCTAAATAA T C RAB2B Ensembl:ENSG00000129472 Protein coding 3'UTR GSE38233;GSE100210;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,KYSE180 cell line chr14:21460330..21460331 24183664,29129909,32596459 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue Human_RBP_ID_26431557 RMVar_hsa_circ_105125,RMVar_hsa_circ_120911,RMVar_hsa_circ_165206,RMVar_hsa_circ_82966,RMVar_hsa_circ_165207,RMVar_hsa_circ_165205 53471 RMVar_ID_53471 Human_SNP_ID_821781051 A-to-I Human chr14 + 50051032 50051032 50051032 TTTGCAGAAAATCCTGGAGTCTGAAGAAAAAGAGGATCCCAACAAGCCCTCAGGATTCAGAAGTG TTTGCAGAAAATCCTGGAGTCTGAAGAAAAAGGGGATCCCAACAAGCCCTCAGGATTCAGAAGTG A G PDLIM1P1 Ensembl:ENSG00000270788 Pseudogene exon GSE100210 HepG2 cell line chr14:50051031..50051032 29129909 RNA-Seq:(High) rs968268113 Functional Loss SNV ICGC 33..33 33 LAML 2 - 53472 RMVar_ID_53472 Human_SNP_ID_821827776 A-to-I Human chr14 - 92118340 92118340 92118340 GAATAGCCACTGCCCTCCAGCCTGGGCAACATAGCAAGACCTTGTCTCTTTTACAAAAAAAAGTT GAATAGCCACTGCCCTCCAGCCTGGGCAACATTGCAAGACCTTGTCTCTTTTACAAAAAAAAGTT T A NDUFB1 Ensembl:ENSG00000183648 Protein coding intron GSE100210 HepG2 cell line chr14:92118339..92118340 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 6 liver 53473 RMVar_ID_53473 Human_SNP_ID_821842853 A-to-I Human chr14 + 103655403 103655403 103655403 CGGCTCACTGCATCCTCTGCCTCCTGGGCTCAAATGATTCTCCTGCCTCAGCCTCCCAAGTAGCT CGGCTCACTGCATCCTCTGCCTCCTGGGCTCAGATGATTCTCCTGCCTCAGCCTCCCAAGTAGCT A G AL139300.1,KLC1 Ensembl:ENSG00000256500,Ensembl:ENSG00000126214 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells chr14:103655403..103655404 24183664 RNA-Seq:(High) rs1366806883 Functional Loss SNV ICGC 33..33 33 MALY 1 - RMVar_hsa_circ_124329,RMVar_hsa_circ_16874,RMVar_hsa_circ_169560,RMVar_hsa_circ_315490,RMVar_hsa_circ_169563,RMVar_hsa_circ_95264,RMVar_hsa_circ_353885,RMVar_hsa_circ_363394,RMVar_hsa_circ_53862,RMVar_hsa_circ_53212,RMVar_hsa_circ_169565,RMVar_hsa_circ_169566 53474 RMVar_ID_53474 Human_SNP_ID_821844244 A-to-I Human chr14 + 32616459 32616459 32616459 AAAGAAAGAGATCATGTCCTTTGCAGGAACATAGACGGATCTGGAGGCCATTATCCTTAGCAAAC AAAGAAAGAGATCATGTCCTTTGCAGGAACATGGACGGATCTGGAGGCCATTATCCTTAGCAAAC A G AKAP6 Ensembl:ENSG00000151320 Protein coding intron GSE107867 ASD brains,cerebellum chr14:32616458..32616459 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - RMVar_hsa_circ_13522,RMVar_hsa_circ_104182,RMVar_hsa_circ_80361,RMVar_hsa_circ_165811,RMVar_hsa_circ_28366,RMVar_hsa_circ_165814 53475 RMVar_ID_53475 Human_SNP_ID_821862695 A-to-I Human chr14 - 63123365 63123365 63123365 TCATAGACAATGTACTCATTATATAGTAGACAAGTGTCATTCACACCAGATGAAATCCCAGTCCC TCATAGACAATGTACTCATTATATAGTAGACAGGTGTCATTCACACCAGATGAAATCCCAGTCCC T C AL137191.1 Ensembl:ENSG00000259093 lincRNA exon GSE100210 HepG2 cell line chr14:63123364..63123365 29129909 RNA-Seq:(High) rs943085298 Functional Loss SNV ICGC 33..33 33 LAML 1 - 53476 RMVar_ID_53476 Human_SNP_ID_821875337 A-to-I Human chr14 - 77312496 77312496 77312496 ACCATGCCTGGCTAATTTTTTGTATTTTTAGTAGAGACAGGGTTTTACCATGTTAGCCAGGATGG ACCATGCCTGGCTAATTTTTTGTATTTTTAGTGGAGACAGGGTTTTACCATGTTAGCCAGGATGG T C POMT2 Ensembl:ENSG00000009830 Protein coding intron GSE47997 K562 cells&HepG2 cells chr14:77312495..77312496 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - RMVar_hsa_circ_112122,RMVar_hsa_circ_168157 53477 RMVar_ID_53477 Human_SNP_ID_821879581 A-to-I Human chr14 + 37509883 37509883 37509883 ATATGTACATATATGTAGGCATTTTTTAAATTAAGAAACTGTAGAAATGCTCTGTTCCTCTTCCC ATATGTACATATATGTAGGCATTTTTTAAATTCAGAAACTGTAGAAATGCTCTGTTCCTCTTCCC A C MIPOL1 Ensembl:ENSG00000151338 Protein coding intron GSE100210 HepG2 cell line chr14:37509882..37509883 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 53478 RMVar_ID_53478 Human_SNP_ID_821897285 A-to-I Human chr14 - 77397668 77397668 77397668 TGGCCAGCCTGGTCTTGAACTCCTGACCTCAAATGATCCGCCTGCCTTGGCCTCCCAAAGTGCTG TGGCCAGCCTGGTCTTGAACTCCTGACCTCAAGTGATCCGCCTGCCTTGGCCTCCCAAAGTGCTG T C NOXRED1 Ensembl:ENSG00000165555 Protein coding intron GSE100210 HepG2 cell line chr14:77397667..77397668 29129909 RNA-Seq:(High) rs1245516609 Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 1 prostate RMVar_hsa_circ_168165 53479 RMVar_ID_53479 Human_SNP_ID_821899293 A-to-I Human chr14 - 73598928 73598928 73598928 GTGATCTTGACTCATTGCAACCTCTGCCTCTCAGGTTTGGGAGATTCTCCTGCCTCAGCCTCCTG GTGATCTTGACTCATTGCAACCTCTGCCTCTCGGGTTTGGGAGATTCTCCTGCCTCAGCCTCCTG T C AC005225.2 Ensembl:ENSG00000258603 lincRNA intron GSE100210 HepG2 cell line chr14:73598927..73598928 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 53480 RMVar_ID_53480 Human_SNP_ID_821939102 A-to-I Human chr14 - 55380148 55380148 55380148 CACCTCACAGTTTCAGGCAATCCTCCCTCCTCAGCCTCCTGTGTAGCTGGGATTACAGGCACCCA CACCTCACAGTTTCAGGCAATCCTCCCTCCTCGGCCTCCTGTGTAGCTGGGATTACAGGCACCCA T C ATG14 Ensembl:ENSG00000126775 Protein coding intron GSE100210 HepG2 cell line chr14:55380147..55380148 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_49128,RMVar_hsa_circ_166836,RMVar_hsa_circ_96031,RMVar_hsa_circ_166838,RMVar_hsa_circ_315712,RMVar_hsa_circ_274100 53481 RMVar_ID_53481 Human_SNP_ID_821945506 A-to-I Human chr14 + 55584739 55584739 55584739 ATAACCCTCAAACACAGTATTACATAGCTTCTATGAGGGTAGGCTTTTTGTCTGTTTTATTGATG ATAACCCTCAAACACAGTATTACATAGCTTCTGTGAGGGTAGGCTTTTTGTCTGTTTTATTGATG A G KTN1 Ensembl:ENSG00000126777 Protein coding intron GSE100210 HepG2 cell line chr14:55584738..55584739 29129909 RNA-Seq:(High) rs1031988245 Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 4 breast Human_RBP_ID_3453006,Human_RBP_ID_17562563 RMVar_hsa_circ_166839,RMVar_hsa_circ_105200 53482 RMVar_ID_53482 Human_SNP_ID_821979488 A-to-I Human chr14 - 91506352 91506352 91506352 TTCTTACAACAGTGTCTGATTTAGTGCTATTAACCATATTAAACTCCCATGTTACTGTCTACTTG TTCTTACAACAGTGTCTGATTTAGTGCTATTAGCCATATTAAACTCCCATGTTACTGTCTACTTG T C PPP4R3A Ensembl:ENSG00000100796 Protein coding intron GSE38233 cultured B-cells chr14:91506351..91506352 24183664 RNA-Seq:(High) rs2180886 Functional Loss SNV ICGC 33..33 33 ESCA 1 - GWAS_ID_365,GWAS_ID_366,GWAS_ID_367,GWAS_ID_368,GWAS_ID_369,GWAS_ID_370,GWAS_ID_371,GWAS_ID_372,GWAS_ID_373,GWAS_ID_374,GWAS_ID_375,GWAS_ID_376,GWAS_ID_377,GWAS_ID_378,GWAS_ID_379,GWAS_ID_380,GWAS_ID_381,GWAS_ID_382,GWAS_ID_383,GWAS_ID_384,GWAS_ID_385,GWAS_ID_386,GWAS_ID_387,GWAS_ID_388,GWAS_ID_389,GWAS_ID_390,GWAS_ID_391,GWAS_ID_392,GWAS_ID_393,GWAS_ID_394,GWAS_ID_395,GWAS_ID_396,GWAS_ID_397,GWAS_ID_398,GWAS_ID_399,GWAS_ID_400,GWAS_ID_401,GWAS_ID_402,GWAS_ID_403,GWAS_ID_404,GWAS_ID_405,GWAS_ID_406,GWAS_ID_407,GWAS_ID_408,GWAS_ID_409,GWAS_ID_410,GWAS_ID_411,GWAS_ID_412,GWAS_ID_413,GWAS_ID_414,GWAS_ID_415,GWAS_ID_416,GWAS_ID_417 53483 RMVar_ID_53483 Human_SNP_ID_821987124 A-to-I Human chr14 - 34568834 34568834 34568834 CATGCCTGGCCACTTTAGCCGAGGCTCCAAGAATGTGGCCCACCGGGTCCTCCAAGCCCTGGAGG CATGCCTGGCCACTTTAGCCGAGGCTCCAAGAGTGTGGCCCACCGGGTCCTCCAAGCCCTGGAGG T C SNX6,RPS19P3 Ensembl:ENSG00000129515,Ensembl:ENSG00000240463 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line chr14:34568833..34568834 29129909 RNA-Seq:(High) rs878919435 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue Human_RBP_ID_5095658,Human_RBP_ID_17205856 RMVar_hsa_circ_66521,RMVar_hsa_circ_91409,RMVar_hsa_circ_95775,RMVar_hsa_circ_116058,RMVar_hsa_circ_120246,RMVar_hsa_circ_104373,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_323612,RMVar_hsa_circ_165859,RMVar_hsa_circ_328016,RMVar_hsa_circ_328134,RMVar_hsa_circ_297837,RMVar_hsa_circ_80179,RMVar_hsa_circ_5330,RMVar_hsa_circ_165867,RMVar_hsa_circ_165866 53484 RMVar_ID_53484 Human_SNP_ID_822027659 A-to-I Human chr14 - 21266372 21266372 21266372 TTCTAAGGCCGGGTGTGGCTGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGTGG TTCTAAGGCCGGGTGTGGCTGCTCATGCCTGTCATCCCAGCACTTTGGGAGGCTGAGGCGGGTGG T G HNRNPC Ensembl:ENSG00000092199 Protein coding intron GSE38233 cultured B-cells chr14:21266371..21266372 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_12295459 RMVar_hsa_circ_29581 53485 RMVar_ID_53485 Human_SNP_ID_822059374 A-to-I Human chr14 - 50161253 50161253 50161253 CTCTCTTGCCCAGGCTGGAGTGCAGTGGTGTAATCTCAGCTCACTGCAACCTGCAGCCTTAGCCT CTCTCTTGCCCAGGCTGGAGTGCAGTGGTGTAGTCTCAGCTCACTGCAACCTGCAGCCTTAGCCT T C SOS2 Ensembl:ENSG00000100485 Protein coding intron GSE38233 cultured B-cells chr14:50161252..50161253 24183664 RNA-Seq:(High) rs1276064863 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue RMVar_hsa_circ_882,RMVar_hsa_circ_4561,RMVar_hsa_circ_364959,RMVar_hsa_circ_92072,RMVar_hsa_circ_93929,RMVar_hsa_circ_27177,RMVar_hsa_circ_3497,RMVar_hsa_circ_166409,RMVar_hsa_circ_166408,RMVar_hsa_circ_19219,RMVar_hsa_circ_22481,RMVar_hsa_circ_26113,RMVar_hsa_circ_304397,RMVar_hsa_circ_31194,RMVar_hsa_circ_28874,RMVar_hsa_circ_26744,RMVar_hsa_circ_289323,RMVar_hsa_circ_317333,RMVar_hsa_circ_330518,RMVar_hsa_circ_13057,RMVar_hsa_circ_20037,RMVar_hsa_circ_166438,RMVar_hsa_circ_10486,RMVar_hsa_circ_295742,RMVar_hsa_circ_315037,RMVar_hsa_circ_345497,RMVar_hsa_circ_21734,RMVar_hsa_circ_166441,RMVar_hsa_circ_166443,RMVar_hsa_circ_293708,RMVar_hsa_circ_341497,RMVar_hsa_circ_264783 53486 RMVar_ID_53486 Human_SNP_ID_822106015 A-to-I Human chr14 - 50933716 50933715 50933716 CATATGTATATAATGTGAATATGTAGAAAAAAAGGTCTGGAATTTTAAATACGAAACTGTTCCCT CATATGTATATAATGTGAATATGTAGAAAAAA_GGTCTGGAATTTTAAATACGAAACTGTTCCCT CT C PYGL Ensembl:ENSG00000100504 Protein coding intron GSE100210 HepG2 cell line chr14:50933715..50933716 29129909 RNA-Seq:(High) rs1281119412 Functional Loss DEL ICGC 33..33 33 ESCA 2 - RMVar_hsa_circ_358622,RMVar_hsa_circ_29172,RMVar_hsa_circ_11710,RMVar_hsa_circ_120992,RMVar_hsa_circ_166595 53487 RMVar_ID_53487 Human_SNP_ID_822109938 A-to-I Human chr14 - 44862526 44862526 44862526 ATATGGGGAAAAGAAACATAGCAAGGGTGCATAATGCCTGACTGTCAAAACACTTCTGAATAGAC ATATGGGGAAAAGAAACATAGCAAGGGTGCATGATGCCTGACTGTCAAAACACTTCTGAATAGAC T C DOCK11P1 Ensembl:ENSG00000259000 Pseudogene exon GSE100210 HepG2 cell line chr14:44862525..44862526 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 2 - 53488 RMVar_ID_53488 Human_SNP_ID_822119450 A-to-I Human chr14 + 60142753 60142753 60142753 GGGAGGCCAGGGCGGGTGGATCATTTGAGGTCAGGAGTTTGAGACCAGCCTGGCCAACATGGTGA GGGAGGCCAGGGCGGGTGGATCATTTGAGGTCCGGAGTTTGAGACCAGCCTGGCCAACATGGTGA A C PCNX4 Ensembl:ENSG00000126773 Protein coding 3'UTR GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line chr14:60142752..60142753 31158229 RNA-Seq:(High) rs976790399 Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 3 prostate 53489 RMVar_ID_53489 Human_SNP_ID_822198321 A-to-I Human chr14 - 21246509 21246509 21246509 AGGCTGGAGTGCAGTGGCGCAATCTCCAGCTCACTGCAAGCTCTGCCTCCCGGGTTCACGCCATT AGGCTGGAGTGCAGTGGCGCAATCTCCAGCTCGCTGCAAGCTCTGCCTCCCGGGTTCACGCCATT T C HNRNPC Ensembl:ENSG00000092199 Protein coding intron GSE100210 HepG2 cell line chr14:21246508..21246509 29129909 RNA-Seq:(High) rs549722821 Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_12294020,Human_RBP_ID_25087712 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 53490 RMVar_ID_53490 Human_SNP_ID_822321507 A-to-I Human chr14 + 44120702 44120702 44120702 TCTGCTGCCTCCCAATTGCTAGATCCCAGATCATCATCTGGGGAGGCTGAACACTTCACCCCATG TCTGCTGCCTCCCAATTGCTAGATCCCAGATCGTCATCTGGGGAGGCTGAACACTTCACCCCATG A G - - Other Unknown GSE100210 HepG2 cell line chr14:44120701..44120702 29129909 RNA-Seq:(High) rs878921136 Functional Loss SNV ICGC 33..33 33 LAML 2 - 53491 RMVar_ID_53491 Human_SNP_ID_822345977 A-to-I Human chr14 - 22916548 22916548 22916548 TGATCAAGAATTAGCTCCTCTGGCCAGATGTAATCCTAGTACTTTGGGAGGCTAAGGTGGGTGGA TGATCAAGAATTAGCTCCTCTGGCCAGATGTAGTCCTAGTACTTTGGGAGGCTAAGGTGGGTGGA T C RBM23 Ensembl:ENSG00000100461 Protein coding intron GSE100210 HepG2 cell line chr14:22916547..22916548 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_12299476 RMVar_hsa_circ_86214,RMVar_hsa_circ_165242 53492 RMVar_ID_53492 Human_SNP_ID_822359501 A-to-I Human chr14 - 34858379 34858379 34858379 TTACAGGCATGTGCCTATAATTCCAGTTACTCAGGAGGCTGAGGCAGAATTGCTTGAACCCAGGA TTACAGGCATGTGCCTATAATTCCAGTTACTCGGGAGGCTGAGGCAGAATTGCTTGAACCCAGGA T C BAZ1A Ensembl:ENSG00000198604 Protein coding intron GSE100210 HepG2 cell line chr14:34858378..34858379 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 STAD 1 - RMVar_hsa_circ_83760,RMVar_hsa_circ_165890,RMVar_hsa_circ_165892,RMVar_hsa_circ_87745,RMVar_hsa_circ_111427,RMVar_hsa_circ_120786,RMVar_hsa_circ_165893,RMVar_hsa_circ_372223,RMVar_hsa_circ_165894,RMVar_hsa_circ_165895,RMVar_hsa_circ_115563,RMVar_hsa_circ_165902,RMVar_hsa_circ_303659,RMVar_hsa_circ_111170,RMVar_hsa_circ_165905,RMVar_hsa_circ_165909,RMVar_hsa_circ_264933,RMVar_hsa_circ_365280,RMVar_hsa_circ_165911,RMVar_hsa_circ_165910,RMVar_hsa_circ_113341,RMVar_hsa_circ_332865,RMVar_hsa_circ_165914,RMVar_hsa_circ_165915,RMVar_hsa_circ_371250,RMVar_hsa_circ_374486,RMVar_hsa_circ_165916,RMVar_hsa_circ_314991,RMVar_hsa_circ_165920,RMVar_hsa_circ_165922,RMVar_hsa_circ_340492,RMVar_hsa_circ_294174,RMVar_hsa_circ_283574,RMVar_hsa_circ_165924 53493 RMVar_ID_53493 Human_SNP_ID_822380928 A-to-I Human chr14 + 74483106 74483106 74483106 TAGAAGATTCCTACAGAAAGCAAGTTGAAGTCAACTGCCAACAGTGTATGCTTAAAATCCTAGAT TAGAAGATTCCTACAGAAAGCAAGTTGAAGTCGACTGCCAACAGTGTATGCTTAAAATCCTAGAT A G RAP1AP Ensembl:ENSG00000258769 Pseudogene exon GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr14:74483105..74483106 24183664,29129909 RNA-Seq:(High) rs1200930170 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 12 haematopoietic and lymphoid tissue Human_RBP_ID_6402787 53494 RMVar_ID_53494 Human_SNP_ID_822399082 A-to-I Human chr14 - 50328844 50328844 50328844 GGGACTGCAGGCATGTGCCACTATACTGGCTAATTTTTTTGTATTTTTTGGTAGAGGCAGGGTTT GGGACTGCAGGCATGTGCCACTATACTGGCTATTTTTTTTGTATTTTTTGGTAGAGGCAGGGTTT T A - - Other Unknown GSE100210 HepG2 cell line chr14:50328843..50328844 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 53495 RMVar_ID_53495 Human_SNP_ID_822482233 A-to-I Human chr14 - 55671657 55671657 55671657 AAAATCAAAATGTAGATTAAAAATCATTTCCTACTGTTTCTGCAAGGACGGATTTGTATTTTTCA AAAATCAAAATGTAGATTAAAAATCATTTCCTTCTGTTTCTGCAAGGACGGATTTGTATTTTTCA T A - - Other Unknown GSE38233 cultured B-cells chr14:55671656..55671657 24183664 RNA-Seq:(High) rs1471250846 Functional Loss SNV TCGA 33..33 33 HNSC,LUSC 3 - 53496 RMVar_ID_53496 Human_SNP_ID_822482589 A-to-I Human chr14 + 44120705 44120705 44120705 GCTGCCTCCCAATTGCTAGATCCCAGATCATCATCTGGGGAGGCTGAACACTTCACCCCATGCAG GCTGCCTCCCAATTGCTAGATCCCAGATCATCGTCTGGGGAGGCTGAACACTTCACCCCATGCAG A G - - Other Unknown GSE100210 HepG2 cell line chr14:44120704..44120705 29129909 RNA-Seq:(High) rs878924169 Functional Loss SNV ICGC 33..33 33 LAML 2 - 53497 RMVar_ID_53497 Human_SNP_ID_822489680 A-to-I Human chr14 + 34940129 34940129 34940129 GTCTGGCAACTATGACGGTGAGTGACTGGTATAAGCAACATTGGAAATATGGAGCATTACCAGAT GTCTGGCAACTATGACGGTGAGTGACTGGTATGAGCAACATTGGAAATATGGAGCATTACCAGAT A G IGBP1P1 Ensembl:ENSG00000226677 Pseudogene exon GSE100210 HepG2 cell line chr14:34940128..34940129 29129909 RNA-Seq:(High) rs879180402 Functional Loss SNV ICGC 33..33 33 LAML 2 - 53498 RMVar_ID_53498 Human_SNP_ID_822498844 A-to-I Human chr14 + 55135779 55135779 55135779 TAGAGACAGGGTTTTGCCATATTGCCCAGGCTAGTCTTGAACTCTTGGGCTCAAGCGATTTGCCC TAGAGACAGGGTTTTGCCATATTGCCCAGGCTGGTCTTGAACTCTTGGGCTCAAGCGATTTGCCC A G LGALS3 Ensembl:ENSG00000131981 Protein coding intron GSE100210 HepG2 cell line chr14:55135778..55135779 29129909 RNA-Seq:(High) rs1343045395 Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_8405645 RMVar_hsa_circ_4779 53499 RMVar_ID_53499 Human_SNP_ID_822545153 A-to-I Human chr14 + 35024844 35024844 35024844 CGCCTCCTGGGTTCAAGCTATTCTCCTGCCTCAGTCTCCCGAGTAGCTGGGATTTCAAGCACGTG CGCCTCCTGGGTTCAAGCTATTCTCCTGCCTCGGTCTCCCGAGTAGCTGGGATTTCAAGCACGTG A G SRP54 Ensembl:ENSG00000100883 Protein coding intron GSE100210 HepG2 cell line chr14:35024843..35024844 29129909 RNA-Seq:(High) rs1214663984 Functional Loss SNV ICGC 33..33 33 ESCA 1 - 53500 RMVar_ID_53500 Human_SNP_ID_822585964 A-to-I Human chr14 - 35109729 35109729 35109729 AATATTGGCTGGGCACAGTGGCTCACACCTGTAATCCCAGCAGTTTTGGAGGCTGAGGTGAGAGG AATATTGGCTGGGCACAGTGGCTCACACCTGTGATCCCAGCAGTTTTGGAGGCTGAGGTGAGAGG T C PPP2R3C Ensembl:ENSG00000092020 Protein coding intron GSE100210 HepG2 cell line chr14:35109728..35109729 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue RMVar_hsa_circ_28180,RMVar_hsa_circ_99186,RMVar_hsa_circ_306869,RMVar_hsa_circ_165956,RMVar_hsa_circ_165958,RMVar_hsa_circ_339978,RMVar_hsa_circ_165963,RMVar_hsa_circ_368616,RMVar_hsa_circ_40987,RMVar_hsa_circ_361349,RMVar_hsa_circ_269784,RMVar_hsa_circ_321296,RMVar_hsa_circ_165971,RMVar_hsa_circ_57151,RMVar_hsa_circ_298359,RMVar_hsa_circ_165972 53501 RMVar_ID_53501 Human_SNP_ID_822613484 A-to-I Human chr14 - 22914735 22914735 22914735 CAGGTGATCCACCCACCTTGGCCTCCCAAAGTACTGGGATTACAGGGTGAGCCACCACGGCTGGC CAGGTGATCCACCCACCTTGGCCTCCCAAAGTGCTGGGATTACAGGGTGAGCCACCACGGCTGGC T C RBM23 Ensembl:ENSG00000100461 Protein coding intron GSE38233 cultured B-cells chr14:22914734..22914735 24183664 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 5 prostate RMVar_hsa_circ_86214,RMVar_hsa_circ_165242 53502 RMVar_ID_53502 Human_SNP_ID_822622870 A-to-I Human chr14 + 103485373 103485373 103485373 ATAGTGTACTGTAGCCTTGAACTCCTGGGCTCAAATGATCCTCCTGTGTTGGCTTCTTGAGTAGC ATAGTGTACTGTAGCCTTGAACTCCTGGGCTCCAATGATCCTCCTGTGTTGGCTTCTTGAGTAGC A C MARK3 Ensembl:ENSG00000075413 Protein coding intron GSE100210 HepG2 cell line chr14:103485373..103485374 29129909 RNA-Seq:(High) rs949466261 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_12281560 RMVar_hsa_circ_169509,RMVar_hsa_circ_323142,RMVar_hsa_circ_169517,RMVar_hsa_circ_95136,RMVar_hsa_circ_169518,RMVar_hsa_circ_46555,RMVar_hsa_circ_169535,RMVar_hsa_circ_325968,RMVar_hsa_circ_363113,RMVar_hsa_circ_169537,RMVar_hsa_circ_169538,RMVar_hsa_circ_327373,RMVar_hsa_circ_328498,RMVar_hsa_circ_307718 53503 RMVar_ID_53503 Human_SNP_ID_822664638 A-to-I Human chr14 + 73915522 73915522 73915522 ACCATGCCTGGCTAATTTTTGTTTTTTTTAGTAGAGATGGGGTTTCACCATGTTGGTCAGGCTGG ACCATGCCTGGCTAATTTTTGTTTTTTTTAGTGGAGATGGGGTTTCACCATGTTGGTCAGGCTGG A G ZNF410,AC005520.3 Ensembl:ENSG00000119725,Ensembl:ENSG00000258653 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells chr14:73915521..73915522 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_167815,RMVar_hsa_circ_83272,RMVar_hsa_circ_316748,RMVar_hsa_circ_29919,RMVar_hsa_circ_349855,RMVar_hsa_circ_39439,RMVar_hsa_circ_373197,RMVar_hsa_circ_167825,RMVar_hsa_circ_36365,RMVar_hsa_circ_167827,RMVar_hsa_circ_345392 53504 RMVar_ID_53504 Human_SNP_ID_822667997 A-to-I Human chr14 - 52665226 52665226 52665226 GTCATCTCTGCTTACCGCAACCTCTGCCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTG GTCATCTCTGCTTACCGCAACCTCTGCCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTG T C ERO1A Ensembl:ENSG00000197930 Protein coding intron GSE38233 cultured B-cells chr14:52665225..52665226 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_3785,RMVar_hsa_circ_305776,RMVar_hsa_circ_58052,RMVar_hsa_circ_298218,RMVar_hsa_circ_364618,RMVar_hsa_circ_166705,RMVar_hsa_circ_166707,RMVar_hsa_circ_292235,RMVar_hsa_circ_105987,RMVar_hsa_circ_31672,RMVar_hsa_circ_78157,RMVar_hsa_circ_166708,RMVar_hsa_circ_19422 53505 RMVar_ID_53505 Human_SNP_ID_822677296 A-to-I Human chr14 - 100338944 100338944 100338944 ATGACACCACGCCCAGCTAATTTTGTAGTTTCAGTAGAGACGGGGTTTCTTCATGTTGGTCAGGC ATGACACCACGCCCAGCTAATTTTGTAGTTTCTGTAGAGACGGGGTTTCTTCATGTTGGTCAGGC T A WARS1 Ensembl:ENSG00000140105 Protein coding intron GSE38233 cultured B-cells chr14:100338943..100338944 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 7 breast RMVar_hsa_circ_3583,RMVar_hsa_circ_92847,RMVar_hsa_circ_127132,RMVar_hsa_circ_108099,RMVar_hsa_circ_169031,RMVar_hsa_circ_82436,RMVar_hsa_circ_91764,RMVar_hsa_circ_169033,RMVar_hsa_circ_169034,RMVar_hsa_circ_169032,RMVar_hsa_circ_169030,RMVar_hsa_circ_277427,RMVar_hsa_circ_355351,RMVar_hsa_circ_362448,RMVar_hsa_circ_53910,RMVar_hsa_circ_169035 53506 RMVar_ID_53506 Human_SNP_ID_822689631 A-to-I Human chr14 + 65279293 65279293 65279293 TGTGCCATGGACGGCATTGTCCCAGATATAGCAGTTGGTACAAAGCGGGGATCTGACGAGCTTTT TGTGCCATGGACGGCATTGTCCCAGATATAGCCGTTGGTACAAAGCGGGGATCTGACGAGCTTTT A C PTBP1P Ensembl:ENSG00000259078 Pseudogene exon GSE38233 cultured B-cells chr14:65279292..65279293 24183664 RNA-Seq:(High) rs1346341846 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_1502899,Human_RBP_ID_1822327,Human_RBP_ID_4298938,Human_RBP_ID_8407410,Human_RBP_ID_19958690,Human_RBP_ID_22798109,Human_RBP_ID_26432639,Human_RBP_ID_26926568,Human_RBP_ID_27227976 53507 RMVar_ID_53507 Human_SNP_ID_822701595 A-to-I Human chr14 + 34940158 34940158 34940158 TATAAGCAACATTGGAAATATGGAGCATTACCAGATCAGGGAATAGCCAAGGCAACACCAGAGGA TATAAGCAACATTGGAAATATGGAGCATTACCGGATCAGGGAATAGCCAAGGCAACACCAGAGGA A G IGBP1P1 Ensembl:ENSG00000226677 Pseudogene exon GSE100210 HepG2 cell line chr14:34940157..34940158 29129909 RNA-Seq:(High) rs879031614 Functional Loss SNV ICGC 33..33 33 LAML 1 - 53508 RMVar_ID_53508 Human_SNP_ID_822705019 A-to-I Human chr14 - 95095993 95095993 95095993 CTGTATTGAAAGACTCGGAATATGGTTGTTTGAAGATTCCACCAAGATGTATGTTTGATCATCCA CTGTATTGAAAGACTCGGAATATGGTTGTTTGTAGATTCCACCAAGATGTATGTTTGATCATCCA T A DICER1 Ensembl:ENSG00000100697 Protein coding CDS GSE100210 HepG2 cell line chr14:95095992..95095993 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 bile_duct adenocarcinoma,biliary_tract adenocarcinoma 6 biliary tract,gallbladder Human_RBP_ID_1501516,Human_RBP_ID_1826453,Human_RBP_ID_8797583,Human_RBP_ID_27648883 RMVar_hsa_circ_96636,RMVar_hsa_circ_122457,RMVar_hsa_circ_113315,RMVar_hsa_circ_105806,RMVar_hsa_circ_168830,RMVar_hsa_circ_168832,RMVar_hsa_circ_93536,RMVar_hsa_circ_168833,RMVar_hsa_circ_168831,RMVar_hsa_circ_168829,RMVar_hsa_circ_69216,RMVar_hsa_circ_24293,RMVar_hsa_circ_81178,RMVar_hsa_circ_168835,RMVar_hsa_circ_117005,RMVar_hsa_circ_46406,RMVar_hsa_circ_168836 53509 RMVar_ID_53509 Human_SNP_ID_822749575 A-to-I Human chr14 + 75595888 75595888 75595888 GACTTTCCTCATTCTGTTCTTGCGTTCCTCTCATTGCTTTCTTGAGGTCTTTTTCTTCTCATACA GACTTTCCTCATTCTGTTCTTGCGTTCCTCTCGTTGCTTTCTTGAGGTCTTTTTCTTCTCATACA A G FLVCR2 Ensembl:ENSG00000119686 Protein coding intron GSE107867 ASD brains,temporal_cortex chr14:75595887..75595888 30559470 RNA-Seq:(High) rs879043070 Functional Loss SNV ICGC 33..33 33 STAD 1 - 53510 RMVar_ID_53510 Human_SNP_ID_822798851 A-to-I Human chr14 + 28264763 28264763 28264763 AAGAGTTCTCACTGTGACAGCCCACCTCGCTCACAGACACCACAAGATACCAACAGAGCTTCTGA AAGAGTTCTCACTGTGACAGCCCACCTCGCTCGCAGACACCACAAGATACCAACAGAGCTTCTGA A G BNIP3P1 Ensembl:ENSG00000197358 Pseudogene exon GSE100210 HepG2 cell line chr14:28264762..28264763 29129909 RNA-Seq:(High) rs1339450406 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_1084923,Human_RBP_ID_8250610 Human_miRNA_ID_1878128 53511 RMVar_ID_53511 Human_SNP_ID_822804464 A-to-I Human chr14 - 60780349 60780349 60780349 ATCTGTCTGATGACTGAACGGATTTCATCCTGAATAGCTTTCTGAGACTTTTCTCTGGGTGCACT ATCTGTCTGATGACTGAACGGATTTCATCCTGGATAGCTTTCTGAGACTTTTCTCTGGGTGCACT T C - - Other Unknown GSE100210 HepG2 cell line chr14:60780348..60780349 29129909 RNA-Seq:(High) rs920787372 Functional Loss SNV ICGC,COSMIC 33..33 33 breast ductal_carcinoma,LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 8 haematopoietic and lymphoid tissue,breast 53512 RMVar_ID_53512 Human_SNP_ID_822819820 A-to-I Human chr14 - 32268597 32268597 32268597 TGTCAGATAAAGAATCACCCAGGCCAGACACAATGGCTCATGCTTGTGATCCCAACACTTTGGGA TGTCAGATAAAGAATCACCCAGGCCAGACACAGTGGCTCATGCTTGTGATCCCAACACTTTGGGA T C - - Other Unknown GSE100210 HepG2 cell line chr14:32268596..32268597 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 53513 RMVar_ID_53513 Human_SNP_ID_822831475 A-to-I Human chr14 - 100335086 100335086 100335086 GGCTGAGCTGGTGCCCGAGGCAGGAAGGAGCCACTCAGGACATGTGGAGCCATCTCTCACGTGGC GGCTGAGCTGGTGCCCGAGGCAGGAAGGAGCCGCTCAGGACATGTGGAGCCATCTCTCACGTGGC T C WARS1 Ensembl:ENSG00000140105 Protein coding intron GSE38233 cultured B-cells chr14:100335085..100335086 24183664 RNA-Seq:(High) rs2234532 Functional Loss SNV ICGC 33..33 33 COCA 5 - RMVar_hsa_circ_92847,RMVar_hsa_circ_124164,RMVar_hsa_circ_127132,RMVar_hsa_circ_108099,RMVar_hsa_circ_169031,RMVar_hsa_circ_82436,RMVar_hsa_circ_91764,RMVar_hsa_circ_169033,RMVar_hsa_circ_169034,RMVar_hsa_circ_169032,RMVar_hsa_circ_169029,RMVar_hsa_circ_169030 53514 RMVar_ID_53514 Human_SNP_ID_822866501 A-to-I Human chr14 + 60397860 60397860 60397860 CATTCACAAACTGAAAGAAAAAGCGAAGAAACAGAAGGGTCGCGGCTTTGGCTCCGAAGAGGGGT CATTCACAAACTGAAAGAAAAAGCGAAGAAACGGAAGGGTCGCGGCTTTGGCTCCGAAGAGGGGT A G RBM8B Ensembl:ENSG00000258427 Pseudogene exon GSE100210 HepG2 cell line chr14:60397859..60397860 29129909 RNA-Seq:(High) rs748686203 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_5095320,Human_RBP_ID_5564058 53515 RMVar_ID_53515 Human_SNP_ID_822884185 A-to-I Human chr14 - 91504485 91504485 91504485 CGATTCTCCCGCCTCAGCCTTACGAGTAGCTGACATTACAGGTGCCTGCCACCACGCCTGGTGAA CGATTCTCCCGCCTCAGCCTTACGAGTAGCTGGCATTACAGGTGCCTGCCACCACGCCTGGTGAA T C PPP4R3A Ensembl:ENSG00000100796 Protein coding intron GSE38233 cultured B-cells chr14:91504484..91504485 24183664 RNA-Seq:(High) rs10139669 Functional Loss SNV ICGC 33..33 33 ESCA 1 - GWAS_ID_312,GWAS_ID_313,GWAS_ID_314,GWAS_ID_315,GWAS_ID_316,GWAS_ID_317,GWAS_ID_318,GWAS_ID_319,GWAS_ID_320,GWAS_ID_321,GWAS_ID_322,GWAS_ID_323,GWAS_ID_324,GWAS_ID_325,GWAS_ID_326,GWAS_ID_327,GWAS_ID_328,GWAS_ID_329,GWAS_ID_330,GWAS_ID_331,GWAS_ID_332,GWAS_ID_333,GWAS_ID_334,GWAS_ID_335,GWAS_ID_336,GWAS_ID_337,GWAS_ID_338,GWAS_ID_339,GWAS_ID_340,GWAS_ID_341,GWAS_ID_342,GWAS_ID_343,GWAS_ID_344,GWAS_ID_345,GWAS_ID_346,GWAS_ID_347,GWAS_ID_348,GWAS_ID_349,GWAS_ID_350,GWAS_ID_351,GWAS_ID_352,GWAS_ID_353,GWAS_ID_354,GWAS_ID_355,GWAS_ID_356,GWAS_ID_357,GWAS_ID_358,GWAS_ID_359,GWAS_ID_360,GWAS_ID_361,GWAS_ID_362,GWAS_ID_363,GWAS_ID_364 53516 RMVar_ID_53516 Human_SNP_ID_822911903 A-to-I Human chr14 - 21363151 21363151 21363151 CGTGTTGTGATAAATTGGATTTTCCATTCACCAGAATGAAATGACTGCAGAAGAGAAGCGAAGAG CGTGTTGTGATAAATTGGATTTTCCATTCACCCGAATGAAATGACTGCAGAAGAGAAGCGAAGAG T G SUPT16H Ensembl:ENSG00000092201 Protein coding intron GSE105773 Glioblastoma cells,U87MG chr14:21363150..21363151 29724793 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 3 head and neck Human_RBP_ID_39143 RMVar_hsa_circ_5128,RMVar_hsa_circ_80881,RMVar_hsa_circ_165153,RMVar_hsa_circ_16434,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_70524 53517 RMVar_ID_53517 Human_SNP_ID_822954051 A-to-I Human chr14 - 93290844 93290844 93290844 CCCATCTCTACCAAAAAATACAAAAATTAGCCAGGCATCATGGTACACGCTTCTAGTCCCAGGTA CCCATCTCTACCAAAAAATACAAAAATTAGCCGGGCATCATGGTACACGCTTCTAGTCCCAGGTA T C BTBD7 Ensembl:ENSG00000011114 Protein coding intron GSE100210 HepG2 cell line chr14:93290843..93290844 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - RMVar_hsa_circ_106641,RMVar_hsa_circ_168727,RMVar_hsa_circ_168735,RMVar_hsa_circ_335723,RMVar_hsa_circ_317187,RMVar_hsa_circ_168741,RMVar_hsa_circ_125150,RMVar_hsa_circ_168739,RMVar_hsa_circ_339866,RMVar_hsa_circ_168736,RMVar_hsa_circ_168740 53518 RMVar_ID_53518 Human_SNP_ID_822964004 A-to-I Human chr14 - 74059451 74059451 74059451 CCTCAGGTGATCCGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCACACC CCTCAGGTGATCCGCCTGCCTCGGCCTCCCAAGGTGCTGGGATTACAGGCATGAGCCACCACACC T C ALDH6A1 Ensembl:ENSG00000119711 Protein coding 3'UTR GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829 esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line chr14:74059450..74059451 29796672,31158229 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue 53519 RMVar_ID_53519 Human_SNP_ID_822975251 A-to-I Human chr14 + 102639365 102639365 102639365 GGTTTCACTGCAGCCTGGACCTCCTGGACACAAATGATCCTCCTACCTCAGCCTTCTCCTCCCCT GGTTTCACTGCAGCCTGGACCTCCTGGACACACATGATCCTCCTACCTCAGCCTTCTCCTCCCCT A C RCOR1 Ensembl:ENSG00000089902 Protein coding intron GSE100210 HepG2 cell line chr14:102639365..102639366 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_6325585 53520 RMVar_ID_53520 Human_SNP_ID_823022813 A-to-I Human chr14 - 21162682 21162682 21162682 TTATCTGATGGTTTTGGTGGTTTTGGAATCATAATACCAGAGGATGCCATGACCCGGCTGTTGGT TTATCTGATGGTTTTGGTGGTTTTGGAATCATGATACCAGAGGATGCCATGACCCGGCTGTTGGT T C - - Other Unknown GSE100210 HepG2 cell line chr14:21162681..21162682 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 1 - 53521 RMVar_ID_53521 Human_SNP_ID_823056962 A-to-I Human chr14 + 39324700 39324700 39324700 ACGATCTCGGTTCACTGCAACCCCTTCCTCTCAGGTTCAAATGATTCTTGTTCCTTAGCTTCCCG ACGATCTCGGTTCACTGCAACCCCTTCCTCTCTGGTTCAAATGATTCTTGTTCCTTAGCTTCCCG A T MIA2 Ensembl:ENSG00000150527 Protein coding intron GSE100210 HepG2 cell line chr14:39324699..39324700 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_55578,RMVar_hsa_circ_357844,RMVar_hsa_circ_279700,RMVar_hsa_circ_284519,RMVar_hsa_circ_83225,RMVar_hsa_circ_166126,RMVar_hsa_circ_166127,RMVar_hsa_circ_13978,RMVar_hsa_circ_166132,RMVar_hsa_circ_334404,RMVar_hsa_circ_345510,RMVar_hsa_circ_166134,RMVar_hsa_circ_62818,RMVar_hsa_circ_17846,RMVar_hsa_circ_66339,RMVar_hsa_circ_93576,RMVar_hsa_circ_166135,RMVar_hsa_circ_358623,RMVar_hsa_circ_55553,RMVar_hsa_circ_302859,RMVar_hsa_circ_33419,RMVar_hsa_circ_290726,RMVar_hsa_circ_166136,RMVar_hsa_circ_289144,RMVar_hsa_circ_308040,RMVar_hsa_circ_166137,RMVar_hsa_circ_344812,RMVar_hsa_circ_166138,RMVar_hsa_circ_365935,RMVar_hsa_circ_322673,RMVar_hsa_circ_363396 53522 RMVar_ID_53522 Human_SNP_ID_823070490 A-to-I Human chr14 - 64333091 64333091 64333091 TTGTGATTATCAAGGTCAGGATATCAAGACCAACCTGGCTAACACGGTGAAACCCCATCTCTACT TTGTGATTATCAAGGTCAGGATATCAAGACCAGCCTGGCTAACACGGTGAAACCCCATCTCTACT T C ESR2,AL161756.1 Ensembl:ENSG00000140009,Ensembl:ENSG00000214770 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line chr14:64333090..64333091 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 53523 RMVar_ID_53523 Human_SNP_ID_823082974 A-to-I Human chr14 - 19300991 19300991 19300991 GTGCAAGGAGAACAGCTGGTTCCCGCCGGGGCAGGGAAGCGTGGACGGTGTGGGCTCAGGCGCCT GTGCAAGGAGAACAGCTGGTTCCCGCCGGGGCGGGGAAGCGTGGACGGTGTGGGCTCAGGCGCCT T C AL589743.1 Ensembl:ENSG00000244306 Pseudogene intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr14:19300990..19300991 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_5563687,Human_RBP_ID_17363570,Human_RBP_ID_22711254,Human_RBP_ID_26778255 53524 RMVar_ID_53524 Human_SNP_ID_823096867 A-to-I Human chr14 - 22946959 22946958 22946959 CCAATATGGTGAAACCCTGTCTCTACTAAAAAATACAAAAATTAGCTGGGCATGGTGGCATGTGC CCAATATGGTGAAACCCTGTCTCTACTAAAAA_TACAAAAATTAGCTGGGCATGGTGGCATGTGC AT A AL132780.3,HAUS4 Ensembl:ENSG00000259132,Ensembl:ENSG00000092036 Protein coding,Protein coding intron,intron GSE47997 K562 cells&HepG2 cells chr14:22946958..22946959 23474544 RNA-Seq:(High) rs1316897216 Functional Loss DEL ICGC 33..33 33 COCA 1 - RMVar_hsa_circ_107309,RMVar_hsa_circ_165271 53525 RMVar_ID_53525 Human_SNP_ID_823107581 A-to-I Human chr14 - 50937814 50937814 50937814 TTATTTCAGAGGGTATATTACCTCTCTCTGGAATTTTACATGGGCCGAACATTACAGAACACCAT TTATTTCAGAGGGTATATTACCTCTCTCTGGACTTTTACATGGGCCGAACATTACAGAACACCAT T G PYGL Ensembl:ENSG00000100504 Protein coding CDS GSE100210 HepG2 cell line chr14:50937813..50937814 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus Human_RBP_ID_446864,Human_RBP_ID_998553,Human_RBP_ID_17849200,Human_RBP_ID_26808043 Human_Splice_Rec_1513664,Human_Splice_Rec_1513665,Human_Splice_Rec_1513700,Human_Splice_Rec_1513701,Human_Splice_Rec_1513782,Human_Splice_Rec_1513783 RMVar_hsa_circ_358622,RMVar_hsa_circ_29172,RMVar_hsa_circ_11710 53526 RMVar_ID_53526 Human_SNP_ID_823128626 A-to-I Human chr14 - 90881543 90881543 90881543 TGAGCCAACATTGTGCCATTGCACTCTGGCCTAGGTAACAAGAGCGAAACTCCGTCTCAGAAACA TGAGCCAACATTGTGCCATTGCACTCTGGCCTGGGTAACAAGAGCGAAACTCCGTCTCAGAAACA T C RPS6KA5 Ensembl:ENSG00000100784 Protein coding intron GSE100210 HepG2 cell line chr14:90881542..90881543 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_18658533 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 53527 RMVar_ID_53527 Human_SNP_ID_823169684 A-to-I Human chr14 + 49610688 49610665 49610688 AGGTTCAAGCAGTTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGTGCCCATGACCATG AGGTTCAAGC_______________________AGTAGCTGGGATTACAGGTGCCCATGACCATG CAGTTCTCCTGCCTCAGCCTCCCA C LRR1 Ensembl:ENSG00000165501 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr14:49610687..49610688 24183664,29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 11..33 33 BRCA 1 - 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,RMVar_hsa_circ_105416,RMVar_hsa_circ_166300 53528 RMVar_ID_53528 Human_SNP_ID_823184242 A-to-I Human chr14 + 64395837 64395837 64395837 GTCAGTGGTGCTGAGATCGAAAAACCCTGATCAAGAAGCTTAATGTGAGTTATTGTGTCATTGTG GTCAGTGGTGCTGAGATCGAAAAACCCTGATCGAGAAGCTTAATGTGAGTTATTGTGTCATTGTG A G MTHFD1 Ensembl:ENSG00000100714 Protein coding intron GSE38233 cultured B-cells chr14:64395836..64395837 24183664 RNA-Seq:(High) rs4902278 Functional Loss SNV ICGC 33..33 33 LAML 1 - GWAS_ID_1157,GWAS_ID_1158,GWAS_ID_1159 53529 RMVar_ID_53529 Human_SNP_ID_823188181 A-to-I Human chr14 - 58425957 58425957 58425957 GCCCGCCACCACGCCCAGCTAATTTTTTTTGTATTTTTATTAGAGACGGGGTTTCACCATGTTGG GCCCGCCACCACGCCCAGCTAATTTTTTTTGTTTTTTTATTAGAGACGGGGTTTCACCATGTTGG T A TIMM9 Ensembl:ENSG00000100575 Protein coding intron GSE38233 cultured B-cells chr14:58425956..58425957 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - RMVar_hsa_circ_37823 53530 RMVar_ID_53530 Human_SNP_ID_823200264 A-to-I Human chr14 + 52779593 52779593 52779593 CTATAAAAAATTAGCTGGGTGCAGCGGCATGCACCTGTAGTCCCAGCTACTTGGGAGGCTGAGGC CTATAAAAAATTAGCTGGGTGCAGCGGCATGCGCCTGTAGTCCCAGCTACTTGGGAGGCTGAGGC A G - - Other Unknown GSE100210 HepG2 cell line chr14:52779592..52779593 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - 53531 RMVar_ID_53531 Human_SNP_ID_823220963 A-to-I Human chr14 - 91603045 91603045 91603045 AAGCAGGCCCAAAACCCAAAAAGGCAAAAGACACAGGCAAAGGCACATCACTCACTAATACTGCA AAGCAGGCCCAAAACCCAAAAAGGCAAAAGACGCAGGCAAAGGCACATCACTCACTAATACTGCA T C CATSPERB Ensembl:ENSG00000133962 Protein coding intron GSE100210 HepG2 cell line chr14:91603044..91603045 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue 53532 RMVar_ID_53532 Human_SNP_ID_823228924 A-to-I Human chr14 - 92119068 92119068 92119068 GGCTCAAGCGATCCATCCGCCTTAGTCTCCCAAAGTGCTGTGGTTACAGGCATGAGCCACCTAGT GGCTCAAGCGATCCATCCGCCTTAGTCTCCCAGAGTGCTGTGGTTACAGGCATGAGCCACCTAGT T C NDUFB1 Ensembl:ENSG00000183648 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line chr14:92119067..92119068 31158229 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 haematopoietic and lymphoid tissue 53533 RMVar_ID_53533 Human_SNP_ID_823275262 A-to-I Human chr14 - 63495862 63495862 63495862 ACATAGGGAAACCTTGTCTCTACAAAAATCAAAGAAACTAGCTGGGCAAGGTGGTACATGCCTGT ACATAGGGAAACCTTGTCTCTACAAAAATCAATGAAACTAGCTGGGCAAGGTGGTACATGCCTGT T A PPP2R5E Ensembl:ENSG00000154001 Protein coding intron GSE47997 K562 cells&HepG2 cells chr14:63495861..63495862 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_6368552 RMVar_hsa_circ_23038,RMVar_hsa_circ_20209 53534 RMVar_ID_53534 Human_SNP_ID_823287425 A-to-I Human chr14 - 34567469 34567469 34567469 TGTTTTGTTTTTTTGAGACAGAGTCTGGCGCTATTGCCCAGGCTGGAGTGCAGTGGCAATGATCT TGTTTTGTTTTTTTGAGACAGAGTCTGGCGCTGTTGCCCAGGCTGGAGTGCAGTGGCAATGATCT T C SNX6 Ensembl:ENSG00000129515 Protein coding intron GSE38233 cultured B-cells chr14:34567468..34567469 24183664 RNA-Seq:(High) rs552776918 Functional Loss SNV ICGC 33..33 33 MALY 1 - RMVar_hsa_circ_91409,RMVar_hsa_circ_95775,RMVar_hsa_circ_116058,RMVar_hsa_circ_120246,RMVar_hsa_circ_104373,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_165859 53535 RMVar_ID_53535 Human_SNP_ID_823288286 A-to-I Human chr14 + 49600132 49600132 49600132 AGGAGTACGTGCCCACCGTCTTCGACCACTACACAGTCAGCGTCACCGTGGGGGGCAAGCAGTAC AGGAGTACGTGCCCACCGTCTTCGACCACTACGCAGTCAGCGTCACCGTGGGGGGCAAGCAGTAC A G RHOQP1,LRR1 Ensembl:ENSG00000258568,Ensembl:ENSG00000165501 Pseudogene,Protein coding exon,intron GSE100210 HepG2 cell line chr14:49600131..49600132 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue Human_RBP_ID_5564090,Human_RBP_ID_8798396,Human_RBP_ID_17364493,Human_RBP_ID_17848784 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 53536 RMVar_ID_53536 Human_SNP_ID_823297926 A-to-I Human chr14 - 53050077 53050077 53050077 GAGTCCTTTACTGTACCTCTGTTTTGTGGTTCATCACATTCTACCATATATTATAATTACTTATT GAGTCCTTTACTGTACCTCTGTTTTGTGGTTCGTCACATTCTACCATATATTATAATTACTTATT T C DDHD1 Ensembl:ENSG00000100523 Protein coding intron GSE100210 HepG2 cell line chr14:53050076..53050077 29129909 RNA-Seq:(High) rs1322220401 Functional Loss SNV ICGC 33..33 33 STAD 1 - RMVar_hsa_circ_269123 53537 RMVar_ID_53537 Human_SNP_ID_823371463 A-to-I Human chr14 - 75134600 75134600 75134600 ACAAAAAATAGGGGTTACCTAGATAATGCCAAAGTCAGCATTTGTCCTGGGTTCCCTTGTGTGAT ACAAAAAATAGGGGTTACCTAGATAATGCCAAGGTCAGCATTTGTCCTGGGTTCCCTTGTGTGAT T C TMED10 Ensembl:ENSG00000170348 Protein coding 3'UTR GSE100210 HepG2 cell line chr14:75134599..75134600 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_452089,Human_RBP_ID_9045256,Human_RBP_ID_17480343,Human_RBP_ID_19980328,Human_RBP_ID_22386484,Human_RBP_ID_23637009,Human_RBP_ID_26928050,Human_RBP_ID_27228927,Human_RBP_ID_27647789 Human_miRNA_ID_1006058 53538 RMVar_ID_53538 Human_SNP_ID_823393013 A-to-I Human chr14 + 105454772 105454772 105454772 GGGATTACAGGCGCCCGCCATCACGCCCGGCTAATTTTTTTATTTTTAGTAGAGACGGGGTTTCA GGGATTACAGGCGCCCGCCATCACGCCCGGCTTATTTTTTTATTTTTAGTAGAGACGGGGTTTCA A T MTA1 Ensembl:ENSG00000182979 Protein coding intron GSE100210 HepG2 cell line chr14:105454771..105454772;chr14:105454772..105454773 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - RMVar_hsa_circ_14003,RMVar_hsa_circ_39157,RMVar_hsa_circ_10523,RMVar_hsa_circ_63926,RMVar_hsa_circ_169736,RMVar_hsa_circ_124730,RMVar_hsa_circ_304587,RMVar_hsa_circ_169738,RMVar_hsa_circ_32655 53539 RMVar_ID_53539 Human_SNP_ID_829840392 A-to-I Human chr18 - 31962477 31962477 31962477 CTTGTGGTGTCCCTATATTCAGAATTTCCTCCATCAATGATGATGTCACCAATGTCCAACAATGG CTTGTGGTGTCCCTATATTCAGAATTTCCTCCGTCAATGATGATGTCACCAATGTCCAACAATGG T C - - Other Unknown GSE38233 cultured B-cells chr18:31962476..31962477 24183664 RNA-Seq:(High) rs878944841 Functional Loss SNV ICGC 33..33 33 LAML 2 - 53540 RMVar_ID_53540 Human_SNP_ID_829860769 A-to-I Human chr18 - 2652616 2652616 2652616 GTGAAATACTCTATTTTTAAAAAAATAGAGATAGAGTCTCACTATGTTGCCCAGGTTGGTCTCAA GTGAAATACTCTATTTTTAAAAAAATAGAGATTGAGTCTCACTATGTTGCCCAGGTTGGTCTCAA T A AP005061.2 Ensembl:ENSG00000266405 Pseudogene exon GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line chr18:2652615..2652616 31158229 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 53541 RMVar_ID_53541 Human_SNP_ID_829869242 A-to-I Human chr18 + 12067424 12067424 12067424 CCAGGGCCGAGCGGGAAATTAGCCCTGCCGGCACCCGGCCCGATGGGGTTCATGATAGTGTACAT CCAGGGCCGAGCGGGAAATTAGCCCTGCCGGCGCCCGGCCCGATGGGGTTCATGATAGTGTACAT A G - - Other Unknown GSE100210 HepG2 cell line chr18:12067423..12067424 29129909 RNA-Seq:(High) rs958504722 Functional Loss SNV ICGC 33..33 33 LAML 1 - 53542 RMVar_ID_53542 Human_SNP_ID_829897175 A-to-I Human chr18 - 45953631 45953631 45953631 CTCAAGTTTGAGAGGGGATGGAGAAGACCATTAGATGCAACCCTATGGAGGCCAAAGTGATCATA CTCAAGTTTGAGAGGGGATGGAGAAGACCATTGGATGCAACCCTATGGAGGCCAAAGTGATCATA T C EPG5 Ensembl:ENSG00000152223 Protein coding intron GSE100210 HepG2 cell line chr18:45953630..45953631 29129909 RNA-Seq:(High) rs915767641 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue RMVar_hsa_circ_21350,RMVar_hsa_circ_115268,RMVar_hsa_circ_189871,RMVar_hsa_circ_36696,RMVar_hsa_circ_56507 53543 RMVar_ID_53543 Human_SNP_ID_829969026 A-to-I Human chr18 - 26832262 26832262 26832262 TATGCTGCCCTCAGCCCTGGACCAACTCAGCCAACTTAACATTACCTATCCCATGCTGTTCAAAC TATGCTGCCCTCAGCCCTGGACCAACTCAGCCGACTTAACATTACCTATCCCATGCTGTTCAAAC T C AC018371.2 Ensembl:ENSG00000266184 Pseudogene exon GSE100210 HepG2 cell line chr18:26832261..26832262 29129909 RNA-Seq:(High) rs878937893 Functional Loss SNV ICGC 33..33 33 LAML 1 - 53544 RMVar_ID_53544 Human_SNP_ID_830528020 A-to-I Human chr18 - 657352 657352 657352 GCACAGTTCCCACGTTTTCCTGCGGTCTTGTCAACAAAACTGCTGTTTGAGATCTGTTTCCTACA GCACAGTTCCCACGTTTTCCTGCGGTCTTGTCGACAAAACTGCTGTTTGAGATCTGTTTCCTACA T C TYMSOS Ensembl:ENSG00000176912 lincRNA intron GSE38233 cultured B-cells chr18:657351..657352 24183664 RNA-Seq:(High) rs2853741 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_5098818,Human_RBP_ID_5129923 GWAS_ID_1133,GWAS_ID_1134,GWAS_ID_1135,GWAS_ID_1136 RMVar_hsa_circ_122571,RMVar_hsa_circ_188189 53545 RMVar_ID_53545 Human_SNP_ID_830561849 A-to-I Human chr18 - 31963271 31963271 31963271 TCCTTTATCTTTCCTAGGAATACACTTCTAATAATGCAGCCCCCTCTCCACATCAGGGCAATATC TCCTTTATCTTTCCTAGGAATACACTTCTAATGATGCAGCCCCCTCTCCACATCAGGGCAATATC T C - - Other Unknown GSE100210 HepG2 cell line chr18:31963270..31963271 29129909 RNA-Seq:(High) rs879108054 Functional Loss SNV ICGC 33..33 33 LAML 1 - 53546 RMVar_ID_53546 Human_SNP_ID_830597517 A-to-I Human chr18 - 21558124 21558124 21558124 AAAGTTAGCTGGGCGTGGTGGCATGCGCCTGTAGTCCCAGTTTCTTGGTGGGGCTGAGGTGGGAG AAAGTTAGCTGGGCGTGGTGGCATGCGCCTGTTGTCCCAGTTTCTTGGTGGGGCTGAGGTGGGAG T A ESCO1 Ensembl:ENSG00000141446 Protein coding intron GSE100210 HepG2 cell line chr18:21558123..21558124 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - RMVar_hsa_circ_188987,RMVar_hsa_circ_4114,RMVar_hsa_circ_58308,RMVar_hsa_circ_351029,RMVar_hsa_circ_277913,RMVar_hsa_circ_188985,RMVar_hsa_circ_327841,RMVar_hsa_circ_367621,RMVar_hsa_circ_324686,RMVar_hsa_circ_284087,RMVar_hsa_circ_188988,RMVar_hsa_circ_188992,RMVar_hsa_circ_127210,RMVar_hsa_circ_351392,RMVar_hsa_circ_188986,RMVar_hsa_circ_325988,RMVar_hsa_circ_292371,RMVar_hsa_circ_39639,RMVar_hsa_circ_188993 53547 RMVar_ID_53547 Human_SNP_ID_830691910 A-to-I Human chr18 + 12067463 12067463 12067463 CCGATGGGGTTCATGATAGTGTACATGTTTTCACTGGAGTTGGTAGAATCTCCAGGGCTAGGCAT CCGATGGGGTTCATGATAGTGTACATGTTTTCGCTGGAGTTGGTAGAATCTCCAGGGCTAGGCAT A G - - Other Unknown GSE100210 HepG2 cell line chr18:12067462..12067463 29129909 RNA-Seq:(High) rs1241119757 Functional Loss SNV ICGC 33..33 33 LAML 1 - 53548 RMVar_ID_53548 Human_SNP_ID_830783446 A-to-I Human chr18 + 46193043 46193043 46193043 AATAGTGAAACTGGGCATGGTGGCACGTTCCTATAGTCCCAGCTACTTGGGAGACTGAGGCAGGA AATAGTGAAACTGGGCATGGTGGCACGTTCCTCTAGTCCCAGCTACTTGGGAGACTGAGGCAGGA A C C18orf25 Ensembl:ENSG00000152242 Protein coding intron GSE38233 cultured B-cells chr18:46193042..46193043 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 53549 RMVar_ID_53549 Human_SNP_ID_831039550 A-to-I Human chr18 - 710293 710293 710293 CCAGCCTGAGCAACATAGTGAGACCTCGTCTCAACAAAAAAATACAAAAATTAGCTGGGCGTAGT CCAGCCTGAGCAACATAGTGAGACCTCGTCTCTACAAAAAAATACAAAAATTAGCTGGGCGTAGT T A ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE100210 HepG2 cell line chr18:710292..710293 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 5 prostate Human_RBP_ID_6703672,Human_RBP_ID_25379627 RMVar_hsa_circ_267129,RMVar_hsa_circ_104521,RMVar_hsa_circ_188203,RMVar_hsa_circ_84546,RMVar_hsa_circ_188208 53550 RMVar_ID_53550 Human_SNP_ID_831150596 A-to-I Human chr18 + 12963947 12963947 12963947 GTTGGCCAGACTGGTCTTGAACTTCTAACCTCAGGTGATCTGCCTGCCTCGGCCTCCAAGAGTGC GTTGGCCAGACTGGTCTTGAACTTCTAACCTCGGGTGATCTGCCTGCCTCGGCCTCCAAGAGTGC A G SEH1L Ensembl:ENSG00000085415 Protein coding intron GSE100210 HepG2 cell line chr18:12963946..12963947 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 NKTL 1 - RMVar_hsa_circ_21712,RMVar_hsa_circ_309226,RMVar_hsa_circ_94980,RMVar_hsa_circ_188776,RMVar_hsa_circ_69614,RMVar_hsa_circ_188773,RMVar_hsa_circ_188774,RMVar_hsa_circ_78848,RMVar_hsa_circ_119598,RMVar_hsa_circ_373002,RMVar_hsa_circ_346102,RMVar_hsa_circ_188778,RMVar_hsa_circ_188779,RMVar_hsa_circ_188777 53551 RMVar_ID_53551 Human_SNP_ID_831216910 A-to-I Human chr18 - 26832282 26832282 26832282 GAGAAAGGAGGGAAGATAATTATGCTGCCCTCAGCCCTGGACCAACTCAGCCAACTTAACATTAC GAGAAAGGAGGGAAGATAATTATGCTGCCCTCGGCCCTGGACCAACTCAGCCAACTTAACATTAC T C AC018371.2 Ensembl:ENSG00000266184 Pseudogene exon GSE100210 HepG2 cell line chr18:26832281..26832282 29129909 RNA-Seq:(High) rs1273742416 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_5583407 Human_miRNA_ID_1825628,Human_miRNA_ID_1825791 53552 RMVar_ID_53552 Human_SNP_ID_831269297 A-to-I Human chr18 - 12486915 12486915 12486915 CCGGGAGGCGGAGGTTGCGGTGAGCTGAGATCACACCACTGCCCTCCAGCCTTGGCAACAGAGCG CCGGGAGGCGGAGGTTGCGGTGAGCTGAGATCCCACCACTGCCCTCCAGCCTTGGCAACAGAGCG T G SPIRE1 Ensembl:ENSG00000134278 Protein coding intron GSE100210 HepG2 cell line chr18:12486914..12486915 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_25349192 RMVar_hsa_circ_11582,RMVar_hsa_circ_5011,RMVar_hsa_circ_378204,RMVar_hsa_circ_274681,RMVar_hsa_circ_34365,RMVar_hsa_circ_125506,RMVar_hsa_circ_27694,RMVar_hsa_circ_57843,RMVar_hsa_circ_188724,RMVar_hsa_circ_188726,RMVar_hsa_circ_188725,RMVar_hsa_circ_296800,RMVar_hsa_circ_316827,RMVar_hsa_circ_299184,RMVar_hsa_circ_289787,RMVar_hsa_circ_188730,RMVar_hsa_circ_188731,RMVar_hsa_circ_188732,RMVar_hsa_circ_28156,RMVar_hsa_circ_306850,RMVar_hsa_circ_188733 53553 RMVar_ID_53553 Human_SNP_ID_831361995 A-to-I Human chr18 - 1362762 1362762 1362762 ATTTCACATCAACCAGCCTGCTTTAAAACAGAAAGAAGCAATCCTGAAACTCATCTTGAAAAATG ATTTCACATCAACCAGCCTGCTTTAAAACAGAGAGAAGCAATCCTGAAACTCATCTTGAAAAATG T C LINC00470,AP005119.2 Ensembl:ENSG00000132204,Ensembl:ENSG00000265417 lincRNA,Pseudogene intron,exon GSE38233 cultured B-cells chr18:1362761..1362762 24183664 RNA-Seq:(High) rs878868271 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_2533482,Human_RBP_ID_5583295,Human_RBP_ID_17381809,Human_RBP_ID_19028684,Human_RBP_ID_20347657,Human_RBP_ID_22064141 53554 RMVar_ID_53554 Human_SNP_ID_831393968 A-to-I Human chr18 - 12869403 12869403 12869403 TGATACCAGCGCTTTGGAAGGCCGAGGCAGGCAGATTGCTTGAGACCAGGAGTTTGAGACCAGTC TGATACCAGCGCTTTGGAAGGCCGAGGCAGGCGGATTGCTTGAGACCAGGAGTTTGAGACCAGTC T C PTPN2 Ensembl:ENSG00000175354 Protein coding intron GSE100210 HepG2 cell line chr18:12869402..12869403 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 53555 RMVar_ID_53555 Human_SNP_ID_831406266 A-to-I Human chr18 + 50885371 50885371 50885371 AGCAAACGCCAGCTGTACAAAATATTAAAATTAGCCGGGCACAGTGGCTTGTACCTGTAGTCTCA AGCAAACGCCAGCTGTACAAAATATTAAAATTTGCCGGGCACAGTGGCTTGTACCTGTAGTCTCA A T ME2 Ensembl:ENSG00000082212 Protein coding intron GSE38233 cultured B-cells chr18:50885370..50885371 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 15 breast 53556 RMVar_ID_53556 Human_SNP_ID_831445472 A-to-I Human chr18 + 909811 909811 909811 TAATAATATTGTTTTTCTTTCTACAAAGCACTAGAGAATGCACAGATATACTTTGTGGACCAATT TAATAATATTGTTTTTCTTTCTACAAAGCACTGGAGAATGCACAGATATACTTTGTGGACCAATT A G ADCYAP1 Ensembl:ENSG00000141433 Protein coding 3'UTR GSE107867 ASD brains,frontal_cortex chr18:909810..909811 30559470 RNA-Seq:(High) - Functional Loss SNV TCGA 33..33 33 UCEC 1 - 53557 RMVar_ID_53557 Human_SNP_ID_831473019 A-to-I Human chr18 - 21556833 21556833 21556833 AGTTGGGTGTGGTGGCACGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCGCT AGTTGGGTGTGGTGGCACGCGCCTGTAATCCCGGCTACTCAGGAGGCTGAGGCAGGAGAATCGCT T C ESCO1 Ensembl:ENSG00000141446 Protein coding intron GSE47997 K562 cells&HepG2 cells chr18:21556832..21556833 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_188987,RMVar_hsa_circ_4114,RMVar_hsa_circ_58308,RMVar_hsa_circ_351029,RMVar_hsa_circ_277913,RMVar_hsa_circ_188985,RMVar_hsa_circ_327841,RMVar_hsa_circ_367621,RMVar_hsa_circ_324686,RMVar_hsa_circ_284087,RMVar_hsa_circ_188988,RMVar_hsa_circ_188992,RMVar_hsa_circ_127210,RMVar_hsa_circ_351392,RMVar_hsa_circ_188986,RMVar_hsa_circ_325988,RMVar_hsa_circ_292371,RMVar_hsa_circ_39639,RMVar_hsa_circ_188993 53558 RMVar_ID_53558 Human_SNP_ID_831571906 A-to-I Human chr18 + 21616621 21616621 21616621 CTTGTGATCCACCCGCCTTGGCCTCCCAAAGTACTGGGATTACAGGCGTGAGCCACCATGCCTGA CTTGTGATCCACCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCATGCCTGA A G SNRPD1 Ensembl:ENSG00000167088 Protein coding intron GSE100210 HepG2 cell line chr18:21616620..21616621 29129909 RNA-Seq:(High) rs1365794157 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue Human_RBP_ID_25352747 RMVar_hsa_circ_124957,RMVar_hsa_circ_189006 53559 RMVar_ID_53559 Human_SNP_ID_831578734 A-to-I Human chr18 + 12912898 12912898 12912898 AGAGAACATGGCGGCCCAGAGGGAATGGACCCAGATGGTGTCATCTAGAGCAACTGGGATGAGAT AGAGAACATGGCGGCCCAGAGGGAATGGACCCCGATGGTGTCATCTAGAGCAACTGGGATGAGAT A C EIF4A2P1 Ensembl:ENSG00000267336 Pseudogene exon GSE38233 cultured B-cells chr18:12912897..12912898 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_17381928 Human_miRNA_ID_1872310 53560 RMVar_ID_53560 Human_SNP_ID_831626354 A-to-I Human chr18 + 74390250 74390250 74390250 TGAGCCTTGATCTGGGCGACCATTTCCTGGCCAGTCACCTCAAGGGTGTGTAGCTCCTGGGCGCG TGAGCCTTGATCTGGGCGACCATTTCCTGGCCGGTCACCTCAAGGGTGTGTAGCTCCTGGGCGCG A G - - Other Unknown GSE100210 HepG2 cell line chr18:74390249..74390250 29129909 RNA-Seq:(High) rs878877212 Functional Loss SNV ICGC 33..33 33 LAML 1 - 53561 RMVar_ID_53561 Human_SNP_ID_831627214 A-to-I Human chr18 + 35253614 35253614 35253614 ATTGAAGGATTTTCCACATTCATTACATTCATAAGGTTTCTCTCCAGTGTGAATTCTTTGATGTT ATTGAAGGATTTTCCACATTCATTACATTCATGAGGTTTCTCTCCAGTGTGAATTCTTTGATGTT A G ZNF397 Ensembl:ENSG00000186812 Protein coding intron GSE100210 HepG2 cell line chr18:35253614..35253615 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 21 lung 53562 RMVar_ID_53562 Human_SNP_ID_831651318 A-to-I Human chr18 + 3601937 3601937 3601937 AGGCTGAGGCAGGCGAATCGCTTGAACCCGGGAAGCGGAGATTGCAGTGAGTGGAGATCGGGCCA AGGCTGAGGCAGGCGAATCGCTTGAACCCGGGTAGCGGAGATTGCAGTGAGTGGAGATCGGGCCA A T - - Other Unknown GSE100210 HepG2 cell line chr18:3601937..3601938 29129909 RNA-Seq:(High) rs12960382 Functional Loss SNV ICGC 33..33 33 ESCA 1 - 53563 RMVar_ID_53563 Human_SNP_ID_831697531 A-to-I Human chr18 - 63299837 63299837 63299837 GTGCCGTTTGGCCTGGGCTTGAAGGATACATAAGAGTTTGTTCAAAAAAAAAAAGAAAAAGAAAA GTGCCGTTTGGCCTGGGCTTGAAGGATACATAGGAGTTTGTTCAAAAAAAAAAAGAAAAAGAAAA T C BCL2 Ensembl:ENSG00000171791 Protein coding intron GSE100210 HepG2 cell line chr18:63299836..63299837 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 53564 RMVar_ID_53564 Human_SNP_ID_831728285 A-to-I Human chr18 - 704682 704681 704682 AGAATTGCTTGAACCTGGGAGTTGGAGTTTGCAGTGAGCCGAGATTGCGCCGCTGCACTCCAGCC AGAATTGCTTGAACCTGGGAGTTGGAGTTTGC_GTGAGCCGAGATTGCGCCGCTGCACTCCAGCC CT C ENOSF1 Ensembl:ENSG00000132199 Protein coding intron GSE38233 cultured B-cells chr18:704681..704682 24183664 RNA-Seq:(High) - Functional Loss DEL ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_358210,RMVar_hsa_circ_267129,RMVar_hsa_circ_284124,RMVar_hsa_circ_188199,RMVar_hsa_circ_357752,RMVar_hsa_circ_327287,RMVar_hsa_circ_59154,RMVar_hsa_circ_104521,RMVar_hsa_circ_188203,RMVar_hsa_circ_326575,RMVar_hsa_circ_84546,RMVar_hsa_circ_287133,RMVar_hsa_circ_188207,RMVar_hsa_circ_188208 53565 RMVar_ID_53565 Human_SNP_ID_831836772 A-to-I Human chr18 + 36270846 36270830 36270846 TCAGGCTTTTTGTTTTTTTGAGACAGGGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGCATG TCAGGCTTTTTGTTTTT________________CTCTGTCACCCAGGCTGGAGTGCAGTGGCATG TTTGAGACAGGGTCTCA T MOCOS Ensembl:ENSG00000075643 Protein coding 3'UTR GSE100210 HepG2 cell line chr18:36270845..36270846 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 18..33 33 SKCA 1 - 53566 RMVar_ID_53566 Human_SNP_ID_831866912 A-to-I Human chr18 + 11846569 11846569 11846569 AGCTCATTGTAGTCTCGAACTCCTGGACACAGAGATCCTCCCACCTCAGCATCCCAAGTAGCTGG AGCTCATTGTAGTCTCGAACTCCTGGACACAGGGATCCTCCCACCTCAGCATCCCAAGTAGCTGG A G GNAL Ensembl:ENSG00000141404 Protein coding intron GSE100210 HepG2 cell line chr18:11846568..11846569 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 53567 RMVar_ID_53567 Human_SNP_ID_831878864 A-to-I Human chr18 - 24300989 24300989 24300989 ATGTGCTTTATTAAAGAAAACTGATATTAGCCAGGCGTGGTGGTACACACCTATAGTCCCGGGAG ATGTGCTTTATTAAAGAAAACTGATATTAGCCGGGCGTGGTGGTACACACCTATAGTCCCGGGAG T C OSBPL1A Ensembl:ENSG00000141447 Protein coding intron GSE100210 HepG2 cell line chr18:24300988..24300989 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 3 pancreas Human_RBP_ID_6675035 RMVar_hsa_circ_20957,RMVar_hsa_circ_93897,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_50235,RMVar_hsa_circ_189288,RMVar_hsa_circ_189286,RMVar_hsa_circ_303778,RMVar_hsa_circ_313030,RMVar_hsa_circ_53514,RMVar_hsa_circ_300685,RMVar_hsa_circ_312310,RMVar_hsa_circ_334809,RMVar_hsa_circ_344010,RMVar_hsa_circ_312863,RMVar_hsa_circ_308362,RMVar_hsa_circ_292867,RMVar_hsa_circ_189289,RMVar_hsa_circ_189291,RMVar_hsa_circ_189293,RMVar_hsa_circ_30540,RMVar_hsa_circ_189292,RMVar_hsa_circ_189290 53568 RMVar_ID_53568 Human_SNP_ID_831940209 A-to-I Human chr18 - 28652401 28652401 28652401 GAGGCAGTCTGCACCAGGGCACAGCTGGAGCTAGTAATGACTCTTCACATAGTCCCTGAAGAGGT GAGGCAGTCTGCACCAGGGCACAGCTGGAGCTGGTAATGACTCTTCACATAGTCCCTGAAGAGGT T C - - Other Unknown GSE38233 cultured B-cells chr18:28652400..28652401 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 2 - 53569 RMVar_ID_53569 Human_SNP_ID_831967327 A-to-I Human chr18 + 2772730 2772730 2772730 GTGGCTCGCTGCTCCCTCCACCTGCTGGGCTCAAGTGATCCTTCTGCCTCAGCCCCCCAAGTAGC GTGGCTCGCTGCTCCCTCCACCTGCTGGGCTCTAGTGATCCTTCTGCCTCAGCCCCCCAAGTAGC A T SMCHD1 Ensembl:ENSG00000101596 Protein coding intron GSE100210 HepG2 cell line chr18:2772729..2772730 29129909 RNA-Seq:(High) rs1410997062 Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_110547,RMVar_hsa_circ_188235,RMVar_hsa_circ_36609,RMVar_hsa_circ_58425,RMVar_hsa_circ_188267,RMVar_hsa_circ_15764,RMVar_hsa_circ_370023,RMVar_hsa_circ_366983,RMVar_hsa_circ_339129,RMVar_hsa_circ_62584,RMVar_hsa_circ_43434,RMVar_hsa_circ_188266,RMVar_hsa_circ_39342,RMVar_hsa_circ_14670,RMVar_hsa_circ_188275,RMVar_hsa_circ_10131,RMVar_hsa_circ_102873,RMVar_hsa_circ_376148,RMVar_hsa_circ_188281,RMVar_hsa_circ_188282,RMVar_hsa_circ_332281,RMVar_hsa_circ_326334,RMVar_hsa_circ_22662,RMVar_hsa_circ_375647,RMVar_hsa_circ_336027,RMVar_hsa_circ_316891,RMVar_hsa_circ_188288,RMVar_hsa_circ_188289,RMVar_hsa_circ_188287,RMVar_hsa_circ_298603,RMVar_hsa_circ_23804,RMVar_hsa_circ_19883,RMVar_hsa_circ_73466,RMVar_hsa_circ_376551,RMVar_hsa_circ_54295 53570 RMVar_ID_53570 Human_SNP_ID_832000790 A-to-I Human chr18 + 8740562 8740562 8740562 TGGAGTACAATGGCACAATCCCAGCTCATTGCAACCTCCACCTCCTGGGTTCAAGCGATTTTCCT TGGAGTACAATGGCACAATCCCAGCTCATTGCGACCTCCACCTCCTGGGTTCAAGCGATTTTCCT A G MTCL1 Ensembl:ENSG00000168502 Protein coding intron GSE107867 ASD brains,cerebellum chr18:8740562..8740563 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_114203,RMVar_hsa_circ_188479,RMVar_hsa_circ_82388,RMVar_hsa_circ_108019,RMVar_hsa_circ_188483,RMVar_hsa_circ_188484,RMVar_hsa_circ_75218,RMVar_hsa_circ_268080,RMVar_hsa_circ_341196,RMVar_hsa_circ_113208,RMVar_hsa_circ_188486 53571 RMVar_ID_53571 Human_SNP_ID_832039087 A-to-I Human chr18 - 79377794 79377794 79377794 TTCCCGCACTGAGAGGGAGGGGCCATCCCGGCATCTGTGCCCTGGGCTTGCCTAGCATGGGTGAA TTCCCGCACTGAGAGGGAGGGGCCATCCCGGCCTCTGTGCCCTGGGCTTGCCTAGCATGGGTGAA T G - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr18:79377793..79377794 30559470 RNA-Seq:(High) rs536159627 Functional Loss SNV ICGC 33..33 33 MALY 1 - 53572 RMVar_ID_53572 Human_SNP_ID_832161840 A-to-I Human chr18 - 26832325 26832325 26832325 CTCTGTGTCCACGCTAGCAGGGCCTAATGACAAGTCAGATGTGGAGAAAGGAGGGAAGATAATTA CTCTGTGTCCACGCTAGCAGGGCCTAATGACAGGTCAGATGTGGAGAAAGGAGGGAAGATAATTA T C AC018371.2 Ensembl:ENSG00000266184 Pseudogene exon GSE100210 HepG2 cell line chr18:26832324..26832325 29129909 RNA-Seq:(High) rs972762542 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_4495242,Human_RBP_ID_5583407 53573 RMVar_ID_53573 Human_SNP_ID_832180475 A-to-I Human chr18 + 12067475 12067475 12067475 ATGATAGTGTACATGTTTTCACTGGAGTTGGTAGAATCTCCAGGGCTAGGCATGATGAGGTGTTC ATGATAGTGTACATGTTTTCACTGGAGTTGGTGGAATCTCCAGGGCTAGGCATGATGAGGTGTTC A G - - Other Unknown GSE100210 HepG2 cell line chr18:12067474..12067475 29129909 RNA-Seq:(High) rs1292163960 Functional Loss SNV ICGC 33..33 33 LAML 2 - 53574 RMVar_ID_53574 Human_SNP_ID_832191061 A-to-I Human chr18 + 57669789 57669789 57669789 CTCTCACCTCAGCCTCCCAAGTAGCTGGGACTACAGGTGTGCACCACCACGCCTGGTAATTTTTG CTCTCACCTCAGCCTCCCAAGTAGCTGGGACTGCAGGTGTGCACCACCACGCCTGGTAATTTTTG A G AC027097.2 Ensembl:ENSG00000267787 lincRNA intron GSE100210 HepG2 cell line chr18:57669788..57669789 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - RMVar_hsa_circ_125710,RMVar_hsa_circ_190338 53575 RMVar_ID_53575 Human_SNP_ID_832197825 A-to-I Human chr18 + 32104153 32104153 32104153 CTAGTGACTTAGCCTCCCAAATAGTTGGGATTACAGGTATATGCCACCATGCCTGGCGAATTTTT CTAGTGACTTAGCCTCCCAAATAGTTGGGATTGCAGGTATATGCCACCATGCCTGGCGAATTTTT A G RNF138,AC011825.3 Ensembl:ENSG00000134758,Ensembl:ENSG00000263917 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line chr18:32104152..32104153 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 3 breast Human_RBP_ID_13283974 53576 RMVar_ID_53576 Human_SNP_ID_832232290 A-to-I Human chr18 + 21825707 21825707 21825707 AAACGTTGGTTGTCCCGTAGTAATCAATGCATAGCTACAGCTGGTTGAAGGGGACCAAATCCATT AAACGTTGGTTGTCCCGTAGTAATCAATGCATGGCTACAGCTGGTTGAAGGGGACCAAATCCATT A G MIB1 Ensembl:ENSG00000101752 Protein coding intron GSE100210 HepG2 cell line chr18:21825706..21825707 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine RMVar_hsa_circ_100558,RMVar_hsa_circ_333667,RMVar_hsa_circ_361969,RMVar_hsa_circ_373922,RMVar_hsa_circ_369867,RMVar_hsa_circ_346305,RMVar_hsa_circ_333069,RMVar_hsa_circ_65888,RMVar_hsa_circ_189019,RMVar_hsa_circ_189021,RMVar_hsa_circ_189022,RMVar_hsa_circ_189020,RMVar_hsa_circ_79924,RMVar_hsa_circ_189037,RMVar_hsa_circ_375804,RMVar_hsa_circ_2888,RMVar_hsa_circ_3723,RMVar_hsa_circ_189038,RMVar_hsa_circ_189039,RMVar_hsa_circ_375402,RMVar_hsa_circ_105029,RMVar_hsa_circ_125094,RMVar_hsa_circ_51404,RMVar_hsa_circ_189047,RMVar_hsa_circ_3548,RMVar_hsa_circ_189048,RMVar_hsa_circ_189046,RMVar_hsa_circ_304777,RMVar_hsa_circ_304155,RMVar_hsa_circ_189055,RMVar_hsa_circ_265464,RMVar_hsa_circ_28914,RMVar_hsa_circ_90379,RMVar_hsa_circ_189058,RMVar_hsa_circ_74050,RMVar_hsa_circ_299484,RMVar_hsa_circ_331615,RMVar_hsa_circ_342566,RMVar_hsa_circ_189065,RMVar_hsa_circ_297857,RMVar_hsa_circ_377403,RMVar_hsa_circ_317488,RMVar_hsa_circ_17885,RMVar_hsa_circ_30943,RMVar_hsa_circ_189067 53577 RMVar_ID_53577 Human_SNP_ID_862378831 A-to-I Human chr6 - 53271367 53271367 53271367 TTTTGTATTTTTAGTAGAGACAGGGTTTCACCATTTTGGCCAGGATGGTGTTGATCTCTTGACCT TTTTGTATTTTTAGTAGAGACAGGGTTTCACCGTTTTGGCCAGGATGGTGTTGATCTCTTGACCT T C ELOVL5 Ensembl:ENSG00000012660 Protein coding intron GSE100210 HepG2 cell line chr6:53271366..53271367 29129909 RNA-Seq:(High) rs1381975030 Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_106233,RMVar_hsa_circ_121642,RMVar_hsa_circ_125654,RMVar_hsa_circ_116206,RMVar_hsa_circ_104715,RMVar_hsa_circ_59935,RMVar_hsa_circ_238984,RMVar_hsa_circ_238986,RMVar_hsa_circ_238988,RMVar_hsa_circ_238987,RMVar_hsa_circ_238985,RMVar_hsa_circ_238991,RMVar_hsa_circ_238992,RMVar_hsa_circ_349433 53578 RMVar_ID_53578 Human_SNP_ID_862397961 A-to-I Human chr6 - 100658825 100658825 100658825 TTCTTTCACTTTACATACTACATACATTTTTTATACGGAGTTCATCTCATCTCTGTAGAATGTCA TTCTTTCACTTTACATACTACATACATTTTTTTTACGGAGTTCATCTCATCTCTGTAGAATGTCA T A ASCC3 Ensembl:ENSG00000112249 Protein coding intron GSE100210 HepG2 cell line chr6:100658824..100658825 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 STAD 1 - RMVar_hsa_circ_6113,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_82741,RMVar_hsa_circ_91287,RMVar_hsa_circ_240536,RMVar_hsa_circ_350394,RMVar_hsa_circ_88960,RMVar_hsa_circ_66704,RMVar_hsa_circ_240540,RMVar_hsa_circ_240541,RMVar_hsa_circ_240542,RMVar_hsa_circ_240539,RMVar_hsa_circ_240543,RMVar_hsa_circ_277621,RMVar_hsa_circ_114540,RMVar_hsa_circ_300001,RMVar_hsa_circ_366043,RMVar_hsa_circ_240548,RMVar_hsa_circ_117329,RMVar_hsa_circ_124703,RMVar_hsa_circ_117923,RMVar_hsa_circ_240551,RMVar_hsa_circ_240552,RMVar_hsa_circ_240553,RMVar_hsa_circ_88686,RMVar_hsa_circ_65486,RMVar_hsa_circ_240554,RMVar_hsa_circ_240555,RMVar_hsa_circ_93741,RMVar_hsa_circ_240559,RMVar_hsa_circ_109825,RMVar_hsa_circ_240561,RMVar_hsa_circ_117435,RMVar_hsa_circ_279404,RMVar_hsa_circ_374254,RMVar_hsa_circ_111898,RMVar_hsa_circ_240564,RMVar_hsa_circ_92568,RMVar_hsa_circ_102512,RMVar_hsa_circ_240566,RMVar_hsa_circ_240567,RMVar_hsa_circ_240565,RMVar_hsa_circ_240562,RMVar_hsa_circ_240563,RMVar_hsa_circ_77422,RMVar_hsa_circ_18627,RMVar_hsa_circ_240572,RMVar_hsa_circ_53841,RMVar_hsa_circ_112328,RMVar_hsa_circ_372105,RMVar_hsa_circ_67389,RMVar_hsa_circ_240574,RMVar_hsa_circ_13275,RMVar_hsa_circ_240573,RMVar_hsa_circ_24273,RMVar_hsa_circ_75234,RMVar_hsa_circ_240575,RMVar_hsa_circ_75670,RMVar_hsa_circ_371353,RMVar_hsa_circ_58845,RMVar_hsa_circ_240576 53579 RMVar_ID_53579 Human_SNP_ID_862439777 A-to-I Human chr6 - 44037474 44037474 44037474 ATTCGGGACGCTGAGACATGAGACTTGCTTGAACACAGGAGGTGGAGGTTGCAGTGAGCCGAGAT ATTCGGGACGCTGAGACATGAGACTTGCTTGAGCACAGGAGGTGGAGGTTGCAGTGAGCCGAGAT T C AL109615.3 Ensembl:ENSG00000237686 lincRNA intron GSE100210 HepG2 cell line chr6:44037473..44037474 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 OV 1 - RMVar_hsa_circ_106005,RMVar_hsa_circ_238732 53580 RMVar_ID_53580 Human_SNP_ID_862522069 A-to-I Human chr6 - 104018049 104018042 104018049 CCTCCCTTGCTGCATGACCAGTCAACTTACACAGTACACCAGGGACAGAGTGGACTGAAGCATGA CCTCCCTTGCTGCATGACCAGTCAACTTACAC_______CAGGGACAGAGTGGACTGAAGCATGA GGTGTACT G R3HDM2P2 Ensembl:ENSG00000216817 Pseudogene exon GSE100210 HepG2 cell line chr6:104018048..104018049 29129909 RNA-Seq:(High) rs534702391 Functional Loss DEL ICGC 33..39 33 PBCA 1 - 53581 RMVar_ID_53581 Human_SNP_ID_862526104 A-to-I Human chr6 + 150946370 150946370 150946370 TGGGATTTCACCATGTTGGCCAGGCTGGTCTCAAACGCCTGACCTCAAGTGATCCATCCACCTTG TGGGATTTCACCATGTTGGCCAGGCTGGTCTCGAACGCCTGACCTCAAGTGATCCATCCACCTTG A G MTHFD1L Ensembl:ENSG00000120254 Protein coding intron GSE38233 cultured B-cells chr6:150946370..150946371 24183664 RNA-Seq:(High) rs200337423 Functional Loss SNV ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 4 lung 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_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_84744,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_280794,RMVar_hsa_circ_242315,RMVar_hsa_circ_242316,RMVar_hsa_circ_306737,RMVar_hsa_circ_311801,RMVar_hsa_circ_348341,RMVar_hsa_circ_288971,RMVar_hsa_circ_127783,RMVar_hsa_circ_86612,RMVar_hsa_circ_242317,RMVar_hsa_circ_242319,RMVar_hsa_circ_242321,RMVar_hsa_circ_21076,RMVar_hsa_circ_242322,RMVar_hsa_circ_242320,RMVar_hsa_circ_242318,RMVar_hsa_circ_242324,RMVar_hsa_circ_90387 53582 RMVar_ID_53582 Human_SNP_ID_862549285 A-to-I Human chr6 + 117695087 117695087 117695087 ATGGTGGCTCACGCCTGTGGTCCCAGCTACTCAGAAGGCTGAAGCAGGAGTATAGTTTGAGTTCA ATGGTGGCTCACGCCTGTGGTCCCAGCTACTCGGAAGGCTGAAGCAGGAGTATAGTTTGAGTTCA A G NUS1 Ensembl:ENSG00000153989 Protein coding intron GSE100210 HepG2 cell line chr6:117695086..117695087 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_352886 53583 RMVar_ID_53583 Human_SNP_ID_862588184 A-to-I Human chr6 - 32581567 32581567 32581567 GTGGAGCACCCAAGCGTGACAAGCCCTCTCACAGTGGAATGGAGTGAGCAGCTTTCTGACTTCCT GTGGAGCACCCAAGCGTGACAAGCCCTCTCACGGTGGAATGGAGTGAGCAGCTTTCTGACTTCCT T C HLA-DRB1 Ensembl:ENSG00000196126 Protein coding CDS GSE38233 cultured B-cells chr6:32581566..32581567 24183664 RNA-Seq:(High) rs17878677 Functional Loss SNV COSMIC 33..33 33 thyroid neoplasm 1 head and neck Human_Splice_Rec_759479 Human_miRNA_ID_2047060,Human_miRNA_ID_2672243,Human_miRNA_ID_2968112 RMVar_hsa_circ_93890,RMVar_hsa_circ_237846 53584 RMVar_ID_53584 Human_SNP_ID_862661143 A-to-I Human chr6 + 42889240 42889240 42889240 AGGCAGGCAGATCACTTGAGGTCAGGAGTTCGAGACCAGCCTGACCAACATGGAGAAATTCTGTC AGGCAGGCAGATCACTTGAGGTCAGGAGTTCGGGACCAGCCTGACCAACATGGAGAAATTCTGTC A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE38233 cultured B-cells chr6:42889239..42889240 24183664 RNA-Seq:(High) rs1372301513 Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_15829858 53585 RMVar_ID_53585 Human_SNP_ID_862662290 A-to-I Human chr6 + 42888313 42888313 42888313 AGCTGGGATTACATGCATGTACCACCACACCCAGCTAATTCTTGTATTTTTAGTAGAGATGGAGA AGCTGGGATTACATGCATGTACCACCACACCCGGCTAATTCTTGTATTTTTAGTAGAGATGGAGA A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line chr6:42888312..42888313 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs1455587741 Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_miRNA_ID_756891,Human_miRNA_ID_1360430 53586 RMVar_ID_53586 Human_SNP_ID_862742225 A-to-I Human chr6 + 12895748 12895748 12895748 CATCAGAACTCTACGTATTGATTCTCGAGCCTAGCTGCAAATTAGCATTGCCTGCGGGAATTTCA CATCAGAACTCTACGTATTGATTCTCGAGCCTGGCTGCAAATTAGCATTGCCTGCGGGAATTTCA A G PHACTR1 Ensembl:ENSG00000112137 Protein coding intron GSE107867 ASD brains,frontal_cortex chr6:12895747..12895748 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 UTCA 1 - RMVar_hsa_circ_21632 53587 RMVar_ID_53587 Human_SNP_ID_862760403 A-to-I Human chr6 - 32662428 32662428 32662428 ACATTCTATAAATGCAGGGACCATAGTATGTTATTTATCTTTGAATTCTCAGTGATTGTCAAATT ACATTCTATAAATGCAGGGACCATAGTATGTTGTTTATCTTTGAATTCTCAGTGATTGTCAAATT T C HLA-DQB1 Ensembl:ENSG00000179344 Protein coding exon GSE38233 cultured B-cells chr6:32662427..32662428 24183664 RNA-Seq:(High) rs9274115 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 6 large intestine Human_Splice_Rec_759575 53588 RMVar_ID_53588 Human_SNP_ID_862791442 A-to-I Human chr6 + 25501005 25501005 25501005 AGGATGGTCTGGATCTCCTGACCTCATGATCCACCCGCCTCAGCCTCCCAAAGTGTTGGAATTAC AGGATGGTCTGGATCTCCTGACCTCATGATCCCCCCGCCTCAGCCTCCCAAAGTGTTGGAATTAC A C CARMIL1 Ensembl:ENSG00000079691 Protein coding intron GSE47997 K562 cells&HepG2 cells chr6:25501004..25501005 23474544 RNA-Seq:(High) rs1165269814 Functional Loss SNV ICGC 33..33 33 STAD 1 - RMVar_hsa_circ_7479,RMVar_hsa_circ_335092,RMVar_hsa_circ_28266,RMVar_hsa_circ_75245,RMVar_hsa_circ_11764,RMVar_hsa_circ_29101,RMVar_hsa_circ_237677,RMVar_hsa_circ_237678,RMVar_hsa_circ_237679,RMVar_hsa_circ_54282,RMVar_hsa_circ_376628,RMVar_hsa_circ_304091,RMVar_hsa_circ_316716,RMVar_hsa_circ_53498,RMVar_hsa_circ_314993,RMVar_hsa_circ_308517,RMVar_hsa_circ_237683,RMVar_hsa_circ_237681,RMVar_hsa_circ_237682,RMVar_hsa_circ_53242,RMVar_hsa_circ_24127,RMVar_hsa_circ_287875,RMVar_hsa_circ_298895,RMVar_hsa_circ_8251,RMVar_hsa_circ_55474,RMVar_hsa_circ_25650,RMVar_hsa_circ_303419,RMVar_hsa_circ_290991,RMVar_hsa_circ_282754,RMVar_hsa_circ_31797,RMVar_hsa_circ_21004,RMVar_hsa_circ_237693,RMVar_hsa_circ_237694,RMVar_hsa_circ_237691,RMVar_hsa_circ_237692,RMVar_hsa_circ_25613,RMVar_hsa_circ_116715,RMVar_hsa_circ_41997,RMVar_hsa_circ_55320,RMVar_hsa_circ_237702,RMVar_hsa_circ_55504,RMVar_hsa_circ_344699,RMVar_hsa_circ_368644,RMVar_hsa_circ_55951,RMVar_hsa_circ_53477,RMVar_hsa_circ_237703,RMVar_hsa_circ_237705,RMVar_hsa_circ_46225,RMVar_hsa_circ_237704 53589 RMVar_ID_53589 Human_SNP_ID_862803554 A-to-I Human chr6 + 35300633 35300633 35300633 CTTTGAATTCTTGTAGAAAGTACAATGGCTTCATCCAGTTGGGTTGAGAACAGAGAAAGTAAACC CTTTGAATTCTTGTAGAAAGTACAATGGCTTCGTCCAGTTGGGTTGAGAACAGAGAAAGTAAACC A G DEF6 Ensembl:ENSG00000023892 Protein coding intron GSE38233 cultured B-cells chr6:35300632..35300633 24183664 RNA-Seq:(High) rs1888823 Functional Loss SNV ICGC 33..33 33 SKCA 1 - GWAS_ID_1679,GWAS_ID_1680,GWAS_ID_1681,GWAS_ID_1682,GWAS_ID_1683,GWAS_ID_1684 RMVar_hsa_circ_110847,RMVar_hsa_circ_238039,RMVar_hsa_circ_93192,RMVar_hsa_circ_238040 53590 RMVar_ID_53590 Human_SNP_ID_862878628 A-to-I Human chr6 - 165898265 165898265 165898265 CTACTCTGGTTCAGGCAGAGCTCTGGTGTCCTAGAAGTTGCTACAGAATCTACTGCAGCCACCTT CTACTCTGGTTCAGGCAGAGCTCTGGTGTCCTGGAAGTTGCTACAGAATCTACTGCAGCCACCTT T C PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE100210 HepG2 cell line chr6:165898264..165898265 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 53591 RMVar_ID_53591 Human_SNP_ID_862916076 A-to-I Human chr6 - 32662417 32662417 32662417 ATGCAGGGACCATAGTATGTTATTTATCTTTGAATTCTCAGTGATTGTCAAATTTATATTTGTTG ATGCAGGGACCATAGTATGTTATTTATCTTTGGATTCTCAGTGATTGTCAAATTTATATTTGTTG T C HLA-DQB1 Ensembl:ENSG00000179344 Protein coding exon GSE38233 cultured B-cells chr6:32662416..32662417 24183664 RNA-Seq:(High) rs9274112 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 6 large intestine Human_Splice_Rec_759575 53592 RMVar_ID_53592 Human_SNP_ID_862932427 A-to-I Human chr6 - 88149564 88149564 88149564 TGTTTAAGTATGAGTGGGAGTCGAAAGGCAAAAGTTAGGTTTGTGGATGTGCAAGGACCATGTAA TGTTTAAGTATGAGTGGGAGTCGAAAGGCAAACGTTAGGTTTGTGGATGTGCAAGGACCATGTAA T G CNR1 Ensembl:ENSG00000118432 Protein coding intron GSE107867 ASD brains,frontal_cortex chr6:88149563..88149564 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_18083018 53593 RMVar_ID_53593 Human_SNP_ID_862960414 A-to-I Human chr6 - 117220059 117220059 117220059 TATATATGCCCCTTGGACAAAGACTGAACTTAAGAATACCATGAAAGACTTCCCAGACCCATTCC TATATATGCCCCTTGGACAAAGACTGAACTTACGAATACCATGAAAGACTTCCCAGACCCATTCC T G AB755814 RNACentral:URS000042AFE7 antisense RNA intron GSE100210 HepG2 cell line chr6:117220058..117220059 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 53594 RMVar_ID_53594 Human_SNP_ID_862989448 A-to-I Human chr6 + 110971019 110971019 110971019 TTTTGTATTTTTTGTAGAGATAGGGTTTTGCCATGTTGCCCAGGCTGGTCTCAAACTAGTGAGCT TTTTGTATTTTTTGTAGAGATAGGGTTTTGCCGTGTTGCCCAGGCTGGTCTCAAACTAGTGAGCT A G - - Other Unknown GSE100210 HepG2 cell line chr6:110971018..110971019 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 53595 RMVar_ID_53595 Human_SNP_ID_863001714 A-to-I Human chr6 - 31148934 31148934 31148934 TTGGTCAGGCTGATCTTGAACCCCTGACCTCAAGTGATCCATCTGCCTCGGCCTCCCAAAGTGCT TTGGTCAGGCTGATCTTGAACCCCTGACCTCAGGTGATCCATCTGCCTCGGCCTCCCAAAGTGCT T C CCHCR1 Ensembl:ENSG00000204536 Protein coding intron GSE100210 HepG2 cell line chr6:31148933..31148934 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine Human_Splice_Rec_751336,Human_Splice_Rec_751337,Human_Splice_Rec_751372,Human_Splice_Rec_751373 53596 RMVar_ID_53596 Human_SNP_ID_863016658 A-to-I Human chr6 + 43591430 43591430 43591430 CAGCCTCCACCTCCAGGGTTCAAGTGATCCTCATGCCTCAACCTCCTGAGTAGCTGGGATTATAG CAGCCTCCACCTCCAGGGTTCAAGTGATCCTCGTGCCTCAACCTCCTGAGTAGCTGGGATTATAG A G POLH Ensembl:ENSG00000170734 Protein coding intron GSE100210 HepG2 cell line chr6:43591429..43591430 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_282209,RMVar_hsa_circ_345350,RMVar_hsa_circ_319711,RMVar_hsa_circ_70478,RMVar_hsa_circ_281526,RMVar_hsa_circ_238710,RMVar_hsa_circ_238711,RMVar_hsa_circ_238709 53597 RMVar_ID_53597 Human_SNP_ID_863030128 A-to-I Human chr6 - 35838147 35838147 35838147 GAGCAGAGACTGAGCCGGGCGCGGTGGCTCATACCTGTGATCCCAGCACTTTGGGAGACCAAGGT GAGCAGAGACTGAGCCGGGCGCGGTGGCTCATGCCTGTGATCCCAGCACTTTGGGAGACCAAGGT T C SRPK1 Ensembl:ENSG00000096063 Protein coding intron GSE100210;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BERP35T4 cell line chr6:35838146..35838147 29129909,31158229 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue Human_RBP_ID_26046867 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 53598 RMVar_ID_53598 Human_SNP_ID_863116467 A-to-I Human chr6 + 6898580 6898580 6898580 TGGAGTGCAATGACACCATCTTGGCTCACCACAACCTCCACCTCCGGTTTCAAGTGATTCTCCTG TGGAGTGCAATGACACCATCTTGGCTCACCACTACCTCCACCTCCGGTTTCAAGTGATTCTCCTG A T lnc-RREB1-9,lnc-RREB1-9:2,lnc-RREB1-9:3,lnc-RREB1-9:4,lnc-RREB1-9:5 RNACentral:URS0000D574A6,RNACentral:URS00008B38DF,RNACentral:URS00008B4FA1,RNACentral:URS0000D5DE54,RNACentral:URS0000D5B54A lincRNA,lincRNA,lincRNA,lincRNA,lincRNA exon,exon,exon,exon,exon GSE100210 HepG2 cell line chr6:6898580..6898581 29129909 RNA-Seq:(High) rs6597234 Functional Loss SNV ICGC 33..33 33 ESCA 1 - 53599 RMVar_ID_53599 Human_SNP_ID_863146922 A-to-I Human chr6 - 93310501 93310501 93310501 GCCACCACGCCCGGCTAACTTCTGTATTTTTAATAGAGACGCAATTTCACCATCTTGGCCAGGCT GCCACCACGCCCGGCTAACTTCTGTATTTTTACTAGAGACGCAATTTCACCATCTTGGCCAGGCT T G EPHA7 Ensembl:ENSG00000135333 Protein coding intron GSE100210 HepG2 cell line chr6:93310500..93310501 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_240369,RMVar_hsa_circ_5736,RMVar_hsa_circ_14078,RMVar_hsa_circ_304831,RMVar_hsa_circ_47797 53600 RMVar_ID_53600 Human_SNP_ID_863164786 A-to-I Human chr6 - 87526360 87526351 87526360 GGCATGTGCCACCACACCCAGCTAATTTTTGTATTTCTTAGTAGAGATGGAGTTTCACCATGTTG GGCATGTGCCACCACACCCAGCTAATTTTTGT_________TAGAGATGGAGTTTCACCATGTTG ACTAAGAAAT A RARS2 Ensembl:ENSG00000146282 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr6:87526359..87526360 24183664,29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 33..41 33 LICA 1 - Human_RBP_ID_26030459 RMVar_hsa_circ_27662,RMVar_hsa_circ_103581,RMVar_hsa_circ_8419,RMVar_hsa_circ_369711,RMVar_hsa_circ_240123,RMVar_hsa_circ_240122,RMVar_hsa_circ_2279,RMVar_hsa_circ_13193,RMVar_hsa_circ_77958,RMVar_hsa_circ_40258,RMVar_hsa_circ_240124,RMVar_hsa_circ_6535,RMVar_hsa_circ_13455,RMVar_hsa_circ_283371,RMVar_hsa_circ_348662,RMVar_hsa_circ_44831,RMVar_hsa_circ_240125,RMVar_hsa_circ_240126 53601 RMVar_ID_53601 Human_SNP_ID_863176372 A-to-I Human chr6 - 13790568 13790568 13790568 GGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTAAGGTGTGAACCTGGGAGGCGGAGCTTGTAGTG GGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGTGTGAACCTGGGAGGCGGAGCTTGTAGTG T C MCUR1 Ensembl:ENSG00000050393 Protein coding 3'UTR GSE100210 HepG2 cell line chr6:13790567..13790568 29129909 RNA-Seq:(High) rs1561727889 Functional Loss SNV ICGC 33..33 33 PRAD 1 - RMVar_hsa_circ_7100,RMVar_hsa_circ_109132,RMVar_hsa_circ_331721,RMVar_hsa_circ_237237,RMVar_hsa_circ_62883 53602 RMVar_ID_53602 Human_SNP_ID_863204369 A-to-I Human chr6 - 36544790 36544790 36544790 CAAACTCACTGAAACCTCTGCCTCTCCAGCTCAAGCAATCCTCCCACCTCAGCCTCCTGAGTAGC CAAACTCACTGAAACCTCTGCCTCTCCAGCTCGAGCAATCCTCCCACCTCAGCCTCCTGAGTAGC T C STK38 Ensembl:ENSG00000112079 Protein coding intron GSE99789 esophageal squamous carcinoma cells,EC109 chr6:36544789..36544790 29796672 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 53603 RMVar_ID_53603 Human_SNP_ID_863206928 A-to-I Human chr6 + 72643586 72643586 72643586 ATTCTCAAAGGAAATGCTCATCGGAGCATTTCAGATTTTGGATTTTGGATTAGGGATGCTCAAAC ATTCTCAAAGGAAATGCTCATCGGAGCATTTCCGATTTTGGATTTTGGATTAGGGATGCTCAAAC A C KCNQ5-IT1,KCNQ5 Ensembl:ENSG00000233844,Ensembl:ENSG00000185760 lincRNA,Protein coding intron,intron GSE107867 ASD brains,temporal_cortex chr6:72643585..72643586 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_8270852 RMVar_hsa_circ_72842,RMVar_hsa_circ_239479 53604 RMVar_ID_53604 Human_SNP_ID_863231436 A-to-I Human chr6 + 29944135 29944135 29944135 TTCTGACTCTTCCCGTCAGACCCCCCCAAGACACATATGACCCACCACCCCATCTCTGACCATGA TTCTGACTCTTCCCGTCAGACCCCCCCAAGACGCATATGACCCACCACCCCATCTCTGACCATGA A G HLA-A Ensembl:ENSG00000206503 Protein coding CDS GSE38233 cultured B-cells chr6:29944134..29944135 24183664 RNA-Seq:(High) rs1136749 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,COCA,large_intestine adenocarcinoma 16 head and neck,large intestine Human_Splice_Rec_747844,Human_Splice_Rec_747858,Human_Splice_Rec_747872,Human_Splice_Rec_747886,Human_Splice_Rec_747898,Human_Splice_Rec_747904,Human_Splice_Rec_747918,Human_Splice_Rec_747926,Human_Splice_Rec_747936 53605 RMVar_ID_53605 Human_SNP_ID_863231793 A-to-I Human chr6 - 108786163 108786163 108786163 CGTGCATCAGACCAATGAGGTGAAATCTGGAGAAGCAGTAGAACCCTTGGGCACCAGGATCACCC CGTGCATCAGACCAATGAGGTGAAATCTGGAGGAGCAGTAGAACCCTTGGGCACCAGGATCACCC T C ZNF259P1 Ensembl:ENSG00000219565 Pseudogene exon GSE100210 HepG2 cell line chr6:108786162..108786163 29129909 RNA-Seq:(High) rs972845542 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_18060053 53606 RMVar_ID_53606 Human_SNP_ID_863248921 A-to-I Human chr6 + 122414851 122414822 122414852 GTTGGCCAGGCTGTTCTCAAACTCCTGACCTCAAGTGATCCGCCCACATCGGCCTTTCAAAGTGC GTTG______________________________GTGATCCGCCCACATCGGCCTTTCAAAGTGC GGCCAGGCTGTTCTCAAACTCCTGACCTCAA G HSF2 Ensembl:ENSG00000025156 Protein coding intron GSE100210 HepG2 cell line chr6:122414851..122414852 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 5..34 33 LICA 1 - RMVar_hsa_circ_294680,RMVar_hsa_circ_72263,RMVar_hsa_circ_241248,RMVar_hsa_circ_113855 53607 RMVar_ID_53607 Human_SNP_ID_863290875 A-to-I Human chr6 - 131185037 131185037 131185037 CAGCCTGGGCAAGTTTCCTGTGACAAACAGTCAAGCACGAAAGCGGATCCTAGAACCAGATGACT CAGCCTGGGCAAGTTTCCTGTGACAAACAGTCGAGCACGAAAGCGGATCCTAGAACCAGATGACT T C AL137222.1 Ensembl:ENSG00000218857 Pseudogene exon GSE100210 HepG2 cell line chr6:131185036..131185037 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue 53608 RMVar_ID_53608 Human_SNP_ID_863381259 A-to-I Human chr6 + 43618259 43618259 43618259 CTCACTGCAACCTCCGTCTCTCGGGTTCAAGCAATTCTCCTGCCTCAGCTTCCCGAATAGCTGAG CTCACTGCAACCTCCGTCTCTCGGGTTCAAGCGATTCTCCTGCCTCAGCTTCCCGAATAGCTGAG A G POLH Ensembl:ENSG00000170734 Protein coding 3'UTR GSE47997;GSE100210;GSE99789 K562 cells&HepG2 cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 chr6:43618258..43618259;chr6:43618259..43618260 23474544,29129909,29796672 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_125996,RMVar_hsa_circ_238718 53609 RMVar_ID_53609 Human_SNP_ID_863392894 A-to-I Human chr6 + 124070322 124070322 124070322 ACCTCTGACCAAGAGGCACAGGCTGTGTGTATAATTCTTTACATAATGCACTGACTTCCAACCTA ACCTCTGACCAAGAGGCACAGGCTGTGTGTATGATTCTTTACATAATGCACTGACTTCCAACCTA A G NKAIN2 Ensembl:ENSG00000188580 Protein coding intron GSE107867 ASD brains,frontal_cortex chr6:124070322..124070323 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 53610 RMVar_ID_53610 Human_SNP_ID_863394379 A-to-I Human chr6 + 149772198 149772198 149772198 AAGATCCTGGGGAGCTTCTGAACCCCGAAGGCACCTGCTACCACCGCTCAGTGAAACTTGCTTCA AAGATCCTGGGGAGCTTCTGAACCCCGAAGGCGCCTGCTACCACCGCTCAGTGAAACTTGCTTCA A G PCMT1 Ensembl:ENSG00000120265 Protein coding intron GSE100210 HepG2 cell line chr6:149772197..149772198 29129909 RNA-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_15684516,Human_RBP_ID_27520238 Human_Splice_Rec_822237,Human_Splice_Rec_822313,Human_Splice_Rec_822329 RMVar_hsa_circ_10519,RMVar_hsa_circ_119973,RMVar_hsa_circ_242252,RMVar_hsa_circ_242250,RMVar_hsa_circ_242253,RMVar_hsa_circ_242251,RMVar_hsa_circ_242259,RMVar_hsa_circ_104512,RMVar_hsa_circ_294390,RMVar_hsa_circ_305365,RMVar_hsa_circ_345351,RMVar_hsa_circ_305192,RMVar_hsa_circ_280571,RMVar_hsa_circ_292334,RMVar_hsa_circ_275996,RMVar_hsa_circ_1899,RMVar_hsa_circ_88233,RMVar_hsa_circ_242261,RMVar_hsa_circ_242260,RMVar_hsa_circ_242255,RMVar_hsa_circ_242257,RMVar_hsa_circ_242258,RMVar_hsa_circ_242256,RMVar_hsa_circ_242254 53611 RMVar_ID_53611 Human_SNP_ID_863412299 A-to-I Human chr6 - 24719059 24719059 24719059 TCCGGATGGATTTTAGGGATTGGTCTGGTGTCAGCTGTGTTTTATTGCACACCTAAATCCTGATT TCCGGATGGATTTTAGGGATTGGTCTGGTGTCGGCTGTGTTTTATTGCACACCTAAATCCTGATT T C C6orf62 Ensembl:ENSG00000112308 Protein coding 5'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr6:24719058..24719059 30559470 RNA-Seq:(High) rs1032456210 Functional Loss SNV COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 2 brain Human_RBP_ID_658848,Human_RBP_ID_1045904,Human_RBP_ID_1113025,Human_RBP_ID_1216501,Human_RBP_ID_1326377,Human_RBP_ID_1668610,Human_RBP_ID_2016524,Human_RBP_ID_3803890,Human_RBP_ID_4909664,Human_RBP_ID_7584595,Human_RBP_ID_8639771,Human_RBP_ID_9192702,Human_RBP_ID_15767679,Human_RBP_ID_17419159,Human_RBP_ID_18860346,Human_RBP_ID_21221473,Human_RBP_ID_22618038,Human_RBP_ID_24152724,Human_RBP_ID_27753878 53612 RMVar_ID_53612 Human_SNP_ID_863417770 A-to-I Human chr6 + 42888418 42888418 42888418 GACCTCAAGTGATCCACAAGCCTGGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCAACTGCG GACCTCAAGTGATCCACAAGCCTGGGCCTCCCGAAGTGCTGGGATTACAGGCATGAGCAACTGCG A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE100210 HepG2 cell line chr6:42888417..42888418;chr6:42888418..42888419 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_791029,Human_RBP_ID_26536822 53613 RMVar_ID_53613 Human_SNP_ID_863447609 A-to-I Human chr6 + 42888234 42888234 42888234 TGGAGCGCAGTGGCATGATCTCAGCTCATTGCAGCCTCCACCTCCTGGGTTCAAGTGATTCTGCC TGGAGCGCAGTGGCATGATCTCAGCTCATTGCGGCCTCCACCTCCTGGGTTCAAGTGATTCTGCC A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line chr6:42888233..42888234 29129909,31158229 RNA-Seq:(High) rs1167593296 Functional Loss SNV ICGC 33..33 33 PBCA 1 - 53614 RMVar_ID_53614 Human_SNP_ID_863462834 A-to-I Human chr6 + 30485934 30485934 30485934 CAGACGGGCATGGAGACGCTTCTGGAAGGAACACCGCAATGGCTGCGCAGGGACAGCCCCAGGTC CAGACGGGCATGGAGACGCTTCTGGAAGGAACGCCGCAATGGCTGCGCAGGGACAGCCCCAGGTC A G - - Other Unknown GSE100210 HepG2 cell line chr6:30485933..30485934 29129909 RNA-Seq:(High) rs878885739 Functional Loss SNV ICGC 33..33 33 LAML 2 - 53615 RMVar_ID_53615 Human_SNP_ID_863472879 A-to-I Human chr6 + 128929385 128929385 128929385 ACCTCGAGAGAATACAAAGAAGTTCATCAGTCATGTGAGGATGAGTGATAGCACACCTCCATCTT ACCTCGAGAGAATACAAAGAAGTTCATCAGTCGTGTGAGGATGAGTGATAGCACACCTCCATCTT A G LAMA2 Ensembl:ENSG00000196569 Protein coding intron GSE100210 HepG2 cell line chr6:128929384..128929385 29129909 RNA-Seq:(High) rs1160848173 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 8 haematopoietic and lymphoid tissue 53616 RMVar_ID_53616 Human_SNP_ID_863475819 A-to-I Human chr6 + 36674107 36674107 36674107 AAAGAAAACATCAGAGCTGCTGTTGCAGCAGGATGCAGGCAGATTCAAGACCTGGAGCTCTCTTC AAAGAAAACATCAGAGCTGCTGTTGCAGCAGGGTGCAGGCAGATTCAAGACCTGGAGCTCTCTTC A G LAP3P2 Ensembl:ENSG00000213500 Pseudogene exon GSE100210 HepG2 cell line chr6:36674106..36674107 29129909 RNA-Seq:(High) rs878952682 Functional Loss SNV ICGC 33..33 33 LAML 1 - 53617 RMVar_ID_53617 Human_SNP_ID_863521258 A-to-I Human chr6 + 124038354 124038354 124038354 CTCCTGCCTCAGCCTCCTGCGTATCTGGGATTACAGACACCCACCACCAGGCCCGGATAATTTCT CTCCTGCCTCAGCCTCCTGCGTATCTGGGATTGCAGACACCCACCACCAGGCCCGGATAATTTCT A G NKAIN2 Ensembl:ENSG00000188580 Protein coding intron GSE107867 ASD brains,frontal_cortex chr6:124038353..124038354 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LMS 1 - 53618 RMVar_ID_53618 Human_SNP_ID_863572546 A-to-I Human chr6 - 31810842 31810842 31810842 CCTGATGAGGCCGTAGCATATGGGGCTGCGGTACAAGCAGCCATCCTGATGGGGGACAAGTCTGA CCTGATGAGGCCGTAGCATATGGGGCTGCGGTGCAAGCAGCCATCCTGATGGGGGACAAGTCTGA T C HSPA1L Ensembl:ENSG00000204390 Protein coding CDS GSE100210 HepG2 cell line chr6:31810841..31810842 29129909 RNA-Seq:(High) rs1201797993 Functional Loss SNV COSMIC 33..33 33 cervix squamous_cell_carcinoma 1 uterus 53619 RMVar_ID_53619 Human_SNP_ID_863600058 A-to-I Human chr6 - 73292430 73292430 73292430 ACTTACAGCATTTCTGTCTGTTGCTGGAACCAACACTCTGAAAAAATAAAGATATTCTGCTGCTC ACTTACAGCATTTCTGTCTGTTGCTGGAACCAGCACTCTGAAAAAATAAAGATATTCTGCTGCTC T C KHDC1 Ensembl:ENSG00000135314 Protein coding intron GSE100210 HepG2 cell line chr6:73292429..73292430 29129909 RNA-Seq:(High) rs183513861 Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 2 breast Human_RBP_ID_1675809,Human_RBP_ID_3814536 53620 RMVar_ID_53620 Human_SNP_ID_863661551 A-to-I Human chr6 - 73270433 73270433 73270433 GGAGTCCCGCTCTGTTGCCCAGGTTGGAGTGTAGTCGCAAAATCTCAGCTCACTGCAACCTCTGC GGAGTCCCGCTCTGTTGCCCAGGTTGGAGTGTCGTCGCAAAATCTCAGCTCACTGCAACCTCTGC T G KHDC1 Ensembl:ENSG00000135314 Protein coding intron GSE107867 ASD brains,temporal_cortex chr6:73270433..73270434 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - Human_RBP_ID_22616790 53621 RMVar_ID_53621 Human_SNP_ID_863716785 A-to-I Human chr6 - 7339031 7339031 7339031 ACACTGCTGTGCGCCATGTGTTGCTCAGACAGAGTGTGCTGGGCATCAAGGTGAAGATCATGCTG ACACTGCTGTGCGCCATGTGTTGCTCAGACAGGGTGTGCTGGGCATCAAGGTGAAGATCATGCTG T C AL139095.2,SSR1,CAGE1 Ensembl:ENSG00000220472,Ensembl:ENSG00000124783,Ensembl:ENSG00000164304 Pseudogene,Protein coding,Protein coding exon,intron,intron GSE100210 HepG2 cell line chr6:7339030..7339031 29129909 RNA-Seq:(High) rs878865712 Functional Loss SNV ICGC,COSMIC 33..33 33 STAD,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 11 haematopoietic and lymphoid tissue Human_RBP_ID_170878,Human_RBP_ID_4915462,Human_RBP_ID_18086404 53622 RMVar_ID_53622 Human_SNP_ID_863718660 A-to-I Human chr6 - 105307073 105307073 105307073 AAAACACAATAAGGACTAGGTCAGCTGAATTTACAGGTTAGTAGAATTGCTTTTTTATTGGTCAG AAAACACAATAAGGACTAGGTCAGCTGAATTTCCAGGTTAGTAGAATTGCTTTTTTATTGGTCAG T G PREP Ensembl:ENSG00000085377 Protein coding intron GSE100210 HepG2 cell line chr6:105307072..105307073 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 53623 RMVar_ID_53623 Human_SNP_ID_863760057 A-to-I Human chr6 + 4036805 4036805 4036805 GGCCAGGAGTTCGAGACCAGCCTGGGCAACATAGTGAGACCCCCATCACTACAAAACAAAATATT GGCCAGGAGTTCGAGACCAGCCTGGGCAACATTGTGAGACCCCCATCACTACAAAACAAAATATT A T PRPF4B Ensembl:ENSG00000112739 Protein coding intron GSE38233 cultured B-cells chr6:4036804..4036805 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 2 oesophagus 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_121680,RMVar_hsa_circ_236972,RMVar_hsa_circ_236969,RMVar_hsa_circ_56044,RMVar_hsa_circ_236970 53624 RMVar_ID_53624 Human_SNP_ID_863761615 A-to-I Human chr6 - 149730713 149730712 149730713 CTGCCCAGGCTGCTCTCAAACTCCTGAGCTCAAGCAATCTTCCTGCCTGGGCCTCCCGAGGTATT CTGCCCAGGCTGCTCTCAAACTCCTGAGCTCA_GCAATCTTCCTGCCTGGGCCTCCCGAGGTATT CT C NUP43 Ensembl:ENSG00000120253 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line chr6:149730712..149730713 31158229 RNA-Seq:(High) - Functional Loss DEL ICGC 33..33 33 RECA 1 - Human_RBP_ID_15683659 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 53625 RMVar_ID_53625 Human_SNP_ID_863794781 A-to-I Human chr6 + 63734075 63734075 63734075 GTGTTCTCATAAGTGGGAGCTAAACATTGGATACACATGGACATAAAGATGGGAACAATTGACAC GTGTTCTCATAAGTGGGAGCTAAACATTGGATGCACATGGACATAAAGATGGGAACAATTGACAC A G PHF3 Ensembl:ENSG00000118482 Protein coding intron GSE100210 HepG2 cell line chr6:63734074..63734075 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 3 liver 53626 RMVar_ID_53626 Human_SNP_ID_863901445 A-to-I Human chr6 + 147569088 147569088 147569088 GTGTCTACTAAAAATACAAAAAAAATTAGCTGAGTGTGGTGGTGTGCGCCTGTAATCCCAGCTAC GTGTCTACTAAAAATACAAAAAAAATTAGCTGCGTGTGGTGGTGTGCGCCTGTAATCCCAGCTAC A C SAMD5 Ensembl:ENSG00000203727 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line chr6:147569087..147569088 31158229,32596459 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 53627 RMVar_ID_53627 Human_SNP_ID_863968237 A-to-I Human chr6 + 122859913 122859913 122859913 AAACTTGGCGTAGTACCAAAATGTGGCCAATCAAGGCTTTGAGTAAGTCACAGCAGCGTTCACCA AAACTTGGCGTAGTACCAAAATGTGGCCAATCGAGGCTTTGAGTAAGTCACAGCAGCGTTCACCA A G - - Other Unknown GSE100210 HepG2 cell line chr6:122859912..122859913 29129909 RNA-Seq:(High) rs879143572 Functional Loss SNV ICGC 33..33 33 LAML 2 - 53628 RMVar_ID_53628 Human_SNP_ID_863978722 A-to-I Human chr6 - 26056064 26056064 26056064 AGCCTCCGGGGAAGCCAAGCCCAAGGTTAAAAAGGCGGGCGGAACCAAACCTAAGAAGCCAGTTG AGCCTCCGGGGAAGCCAAGCCCAAGGTTAAAATGGCGGGCGGAACCAAACCTAAGAAGCCAGTTG T A H1-2 Ensembl:ENSG00000187837 Protein coding CDS GSE100210 HepG2 cell line chr6:26056063..26056064 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_658977,Human_RBP_ID_1045983,Human_RBP_ID_1216573,Human_RBP_ID_1668818,Human_RBP_ID_2016674,Human_RBP_ID_4876069,Human_RBP_ID_8141006,Human_RBP_ID_8899074,Human_RBP_ID_9192811,Human_RBP_ID_15769998,Human_RBP_ID_17305953,Human_RBP_ID_17419185,Human_RBP_ID_18071316,Human_RBP_ID_18202478,Human_RBP_ID_18449930,Human_RBP_ID_18860535,Human_RBP_ID_22102274,Human_RBP_ID_22460428,Human_RBP_ID_22772629,Human_RBP_ID_22830329,Human_RBP_ID_23137892,Human_RBP_ID_26353470,Human_RBP_ID_26534353,Human_RBP_ID_26829091,Human_RBP_ID_27093640,Human_RBP_ID_27521851 RMVar_hsa_circ_237733,RMVar_hsa_circ_237735,RMVar_hsa_circ_377187,RMVar_hsa_circ_266433 53629 RMVar_ID_53629 Human_SNP_ID_863978748 A-to-I Human chr6 - 89634886 89634886 89634886 TCCAGCTACTCAGGAGGGCTGCCTCATATTGAACCCGGGAGGCAGAGGCTGCAGTGAGCCGAGAA TCCAGCTACTCAGGAGGGCTGCCTCATATTGAGCCCGGGAGGCAGAGGCTGCAGTGAGCCGAGAA T C LYRM2 Ensembl:ENSG00000083099 Protein coding intron GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831 HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line chr6:89634885..89634886 29129909,29796672,31158229,31158229,31158229,32596459 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 UTCA 1 - Human_RBP_ID_7645000,Human_RBP_ID_15908078,Human_RBP_ID_26540262 53630 RMVar_ID_53630 Human_SNP_ID_864017963 A-to-I Human chr6 + 109173554 109173554 109173554 TTAAGCAGTCCTCCTGCCTCTGCCTCCCAAGTAGCTGGGACTACAGGTGCATGCCACCACACCTG TTAAGCAGTCCTCCTGCCTCTGCCTCCCAAGTGGCTGGGACTACAGGTGCATGCCACCACACCTG A G CCDC162P Ensembl:ENSG00000203799 Pseudogene intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank chr6:109173553..109173554 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_17422775 53631 RMVar_ID_53631 Human_SNP_ID_864058573 A-to-I Human chr6 + 149880896 149880896 149880896 ACATGTTCTGTGCTGGCCAAGTACCTGAGGAGAATCTGAAGAGGACAATGATGGCCTGTGGAGGC ACATGTTCTGTGCTGGCCAAGTACCTGAGGAGGATCTGAAGAGGACAATGATGGCCTGTGGAGGC A G AL355312.3,CCT7P1 Ensembl:ENSG00000268592,Ensembl:ENSG00000217733 lincRNA,Pseudogene intron,exon GSE100210 HepG2 cell line chr6:149880895..149880896 29129909 RNA-Seq:(High) rs878936562 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_1678888,Human_RBP_ID_2011370,Human_RBP_ID_5216128,Human_RBP_ID_8270461,Human_RBP_ID_8634206,Human_RBP_ID_15685336,Human_RBP_ID_18856444,Human_RBP_ID_26533127 Human_miRNA_ID_1844380,Human_miRNA_ID_1869773,Human_miRNA_ID_1906564 53632 RMVar_ID_53632 Human_SNP_ID_864059173 A-to-I Human chr6 - 73633124 73633124 73633124 AGTTTTAGCTGGGTATGGTGGCACACAAGTGCAGTTCCAGCTCCTCAGGAGGCTGAGGCAAGGGG AGTTTTAGCTGGGTATGGTGGCACACAAGTGCTGTTCCAGCTCCTCAGGAGGCTGAGGCAAGGGG T A SLC17A5 Ensembl:ENSG00000119899 Protein coding intron GSE100210 HepG2 cell line chr6:73633123..73633124 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_5441,RMVar_hsa_circ_102225,RMVar_hsa_circ_324398,RMVar_hsa_circ_239539,RMVar_hsa_circ_351066,RMVar_hsa_circ_316837,RMVar_hsa_circ_265052,RMVar_hsa_circ_309535,RMVar_hsa_circ_337473,RMVar_hsa_circ_296668,RMVar_hsa_circ_239549,RMVar_hsa_circ_239541,RMVar_hsa_circ_239543,RMVar_hsa_circ_239542,RMVar_hsa_circ_266367,RMVar_hsa_circ_300173,RMVar_hsa_circ_362807,RMVar_hsa_circ_278846,RMVar_hsa_circ_239548,RMVar_hsa_circ_239551,RMVar_hsa_circ_325046,RMVar_hsa_circ_327311,RMVar_hsa_circ_344852,RMVar_hsa_circ_319445,RMVar_hsa_circ_239550,RMVar_hsa_circ_239552 53633 RMVar_ID_53633 Human_SNP_ID_864180929 A-to-I Human chr6 + 110858764 110858764 110858764 CCATCGGGCTGCAGATGGGCACCAACAAATGCACCAGCCAGTCGGGCATGACCGCGTACAGCACA CCATCGGGCTGCAGATGGGCACCAACAAATGCCCCAGCCAGTCGGGCATGACCGCGTACAGCACA A C CNN2P9 Ensembl:ENSG00000213149 Pseudogene exon GSE100210 HepG2 cell line chr6:110858763..110858764 29129909 RNA-Seq:(High) rs900162570 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_17422369 53634 RMVar_ID_53634 Human_SNP_ID_864300931 A-to-I Human chr6 - 24666595 24666594 24666595 TGCCTTTGTTTTTCAGAGGGCTCTGAACTCCTACTTCGAGCCTCCGGTGGAGGAGAGCGCCTTGG TGCCTTTGTTTTTCAGAGGGCTCTGAACTCCT_CTTCGAGCCTCCGGTGGAGGAGAGCGCCTTGG GT G TDP2 Ensembl:ENSG00000111802 Protein coding CDS GSE100210 HepG2 cell line chr6:24666594..24666595 29129909 RNA-Seq:(High) - Functional Loss DEL TCGA 33..33 33 LUAD 1 - Human_RBP_ID_949102,Human_RBP_ID_22460412,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 53635 RMVar_ID_53635 Human_SNP_ID_864360857 A-to-I Human chr6 + 31978347 31978347 31978347 GTGGCGGGTGGGGGGGTCTCACTGTGTTGCCCAGACTGGTCTCGAACTCCTGTCCTCAATTGATC GTGGCGGGTGGGGGGGTCTCACTGTGTTGCCCCGACTGGTCTCGAACTCCTGTCCTCAATTGATC A C STK19 Ensembl:ENSG00000204344 Protein coding intron GSE100210 HepG2 cell line chr6:31978346..31978347 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 53636 RMVar_ID_53636 Human_SNP_ID_864528788 A-to-I Human chr6 + 30485939 30485939 30485939 GGGCATGGAGACGCTTCTGGAAGGAACACCGCAATGGCTGCGCAGGGACAGCCCCAGGTCCAGTT GGGCATGGAGACGCTTCTGGAAGGAACACCGCGATGGCTGCGCAGGGACAGCCCCAGGTCCAGTT A G lnc-HLA-E-5,lnc-HLA-E-5:2 RNACentral:URS00009B7853,RNACentral:URS00009BA13C lincRNA,lincRNA intron,exon GSE100210 HepG2 cell line chr6:30485938..30485939 29129909 RNA-Seq:(High) rs879208149 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_4910908 53637 RMVar_ID_53637 Human_SNP_ID_864596387 A-to-I Human chr6 + 42888291 42888291 42888291 ATTCTGCCTCAGCCCCTTGATCAGCTGGGATTACATGCATGTACCACCACACCCAGCTAATTCTT ATTCTGCCTCAGCCCCTTGATCAGCTGGGATTGCATGCATGTACCACCACACCCAGCTAATTCTT A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line chr6:42888290..42888291 24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) rs1318315394 Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_4890182 53638 RMVar_ID_53638 Human_SNP_ID_864605050 A-to-I Human chr6 + 28230503 28230503 28230503 ACAGAGGAGTCCTAAGAGGTACCTATTCTTGTATGTGAGAGACAGGACAGTTAGATATGGGAGAA ACAGAGGAGTCCTAAGAGGTACCTATTCTTGTGTGTGAGAGACAGGACAGTTAGATATGGGAGAA A G ZSCAN9 Ensembl:ENSG00000137185 Protein coding intron GSE38233 cultured B-cells chr6:28230502..28230503 24183664 RNA-Seq:(High) rs1233713 Functional Loss SNV ICGC 33..33 33 COCA 4 - Human_RBP_ID_7588269,Human_RBP_ID_10278732,Human_RBP_ID_15775858,Human_RBP_ID_24154880 GWAS_ID_1117,GWAS_ID_1118,GWAS_ID_1119,GWAS_ID_1120,GWAS_ID_1121,GWAS_ID_1122,GWAS_ID_1123,GWAS_ID_1124 RMVar_hsa_circ_237791,RMVar_hsa_circ_87696,RMVar_hsa_circ_237792,RMVar_hsa_circ_237794 53639 RMVar_ID_53639 Human_SNP_ID_864605263 A-to-I Human chr6 - 29732103 29732103 29732103 AAAATTAGCTGGGCATGGTGGCATGAGCCTGTAGTCCTAGGTACCCCAGTGTTTGAGGTGGGAAG AAAATTAGCTGGGCATGGTGGCATGAGCCTGTTGTCCTAGGTACCCCAGTGTTTGAGGTGGGAAG T A HLA-F-AS1 Ensembl:ENSG00000214922 lincRNA intron GSE100210 HepG2 cell line chr6:29732102..29732103 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 53640 RMVar_ID_53640 Human_SNP_ID_864632874 A-to-I Human chr6 - 8008584 8008584 8008584 AGTTTCGCTCTTGTTGCCCAGGCTGGAGTGCAATGGCGCAACCTTGGCTCACTGCAACCTGCGCC AGTTTCGCTCTTGTTGCCCAGGCTGGAGTGCAGTGGCGCAACCTTGGCTCACTGCAACCTGCGCC T C BLOC1S5-TXNDC5 Ensembl:ENSG00000259040 Protein coding intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line chr6:8008583..8008584 31158229 RNA-Seq:(High) rs1216694070 Functional Loss SNV ICGC 33..33 33 PAAD 1 - RMVar_hsa_circ_80608,RMVar_hsa_circ_237089 53641 RMVar_ID_53641 Human_SNP_ID_864648912 A-to-I Human chr6 - 27144945 27144945 27144945 ACTAACAGTACAAAAATTAGGGGGGGCGTGGTAGCATGTGCCCGTAGTCCCAGCTACTCGGGAGG ACTAACAGTACAAAAATTAGGGGGGGCGTGGTGGCATGTGCCCGTAGTCCCAGCTACTCGGGAGG T C lnc-HIST1H2BK-1 RNACentral:URS00008B29CF lincRNA exon GSE38233 cultured B-cells chr6:27144944..27144945 24183664 RNA-Seq:(High) rs12111326 Functional Loss SNV ICGC 33..33 33 SKCA 1 - GWAS_ID_1115,GWAS_ID_1116 RMVar_hsa_circ_78453,RMVar_hsa_circ_125936,RMVar_hsa_circ_237770,RMVar_hsa_circ_237772 53642 RMVar_ID_53642 Human_SNP_ID_864672846 A-to-I Human chr6 + 44446650 44446650 44446650 AGACGTTCAGCGACAACAAGAAAGAGAAAAGGAACTTCAACATAGATATGCTGATTTGCTGCTGG AGACGTTCAGCGACAACAAGAAAGAGAAAAGGGACTTCAACATAGATATGCTGATTTGCTGCTGG A G CDC5L Ensembl:ENSG00000096401 Protein coding CDS GSE100210 HepG2 cell line chr6:44446649..44446650 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus Human_RBP_ID_81308,Human_RBP_ID_1674217,Human_RBP_ID_2022202,Human_RBP_ID_7610366,Human_RBP_ID_15837662,Human_RBP_ID_18539149,Human_RBP_ID_18866840,Human_RBP_ID_26355279,Human_RBP_ID_27099102,Human_RBP_ID_27827750 Human_Splice_Rec_775114 53643 RMVar_ID_53643 Human_SNP_ID_864679885 A-to-I Human chr6 - 116647350 116647350 116647350 TTTTTGTTTGTTTGTTTGTTTTTTTAGACAGAATCTCACTCTGTTGCTCAGGCTGGAGTGCAGTG TTTTTGTTTGTTTGTTTGTTTTTTTAGACAGAGTCTCACTCTGTTGCTCAGGCTGGAGTGCAGTG T C ZUP1 Ensembl:ENSG00000153975 Protein coding intron GSE38233 cultured B-cells chr6:116647349..116647350 24183664 RNA-Seq:(High) rs6568959 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 2 large intestine GWAS_ID_452,GWAS_ID_453,GWAS_ID_454,GWAS_ID_455,GWAS_ID_456,GWAS_ID_457,GWAS_ID_458,GWAS_ID_459,GWAS_ID_460,GWAS_ID_461,GWAS_ID_462,GWAS_ID_463,GWAS_ID_464,GWAS_ID_465,GWAS_ID_466,GWAS_ID_467,GWAS_ID_468,GWAS_ID_469,GWAS_ID_470,GWAS_ID_471,GWAS_ID_472,GWAS_ID_473,GWAS_ID_474,GWAS_ID_475,GWAS_ID_476,GWAS_ID_477,GWAS_ID_478,GWAS_ID_479,GWAS_ID_480,GWAS_ID_481,GWAS_ID_482,GWAS_ID_483,GWAS_ID_484,GWAS_ID_485,GWAS_ID_486,GWAS_ID_487,GWAS_ID_488,GWAS_ID_489,GWAS_ID_490,GWAS_ID_491,GWAS_ID_492,GWAS_ID_493,GWAS_ID_494,GWAS_ID_495,GWAS_ID_496,GWAS_ID_497,GWAS_ID_498,GWAS_ID_499,GWAS_ID_500,GWAS_ID_501,GWAS_ID_502,GWAS_ID_503,GWAS_ID_504,GWAS_ID_505,GWAS_ID_506,GWAS_ID_507,GWAS_ID_508,GWAS_ID_509,GWAS_ID_510,GWAS_ID_511,GWAS_ID_512,GWAS_ID_513,GWAS_ID_514,GWAS_ID_515,GWAS_ID_516,GWAS_ID_517,GWAS_ID_518,GWAS_ID_519,GWAS_ID_520,GWAS_ID_521,GWAS_ID_522,GWAS_ID_523,GWAS_ID_524,GWAS_ID_525,GWAS_ID_526,GWAS_ID_527,GWAS_ID_528,GWAS_ID_529,GWAS_ID_530,GWAS_ID_531,GWAS_ID_532,GWAS_ID_533,GWAS_ID_534,GWAS_ID_535,GWAS_ID_536,GWAS_ID_537,GWAS_ID_538,GWAS_ID_539,GWAS_ID_540,GWAS_ID_541,GWAS_ID_542,GWAS_ID_543,GWAS_ID_544,GWAS_ID_545,GWAS_ID_546,GWAS_ID_547,GWAS_ID_548,GWAS_ID_549,GWAS_ID_550,GWAS_ID_551,GWAS_ID_552,GWAS_ID_553,GWAS_ID_554,GWAS_ID_555,GWAS_ID_556,GWAS_ID_557,GWAS_ID_558,GWAS_ID_559,GWAS_ID_560,GWAS_ID_561,GWAS_ID_562,GWAS_ID_563,GWAS_ID_564,GWAS_ID_565,GWAS_ID_566,GWAS_ID_567,GWAS_ID_568,GWAS_ID_569,GWAS_ID_570,GWAS_ID_571,GWAS_ID_572,GWAS_ID_573,GWAS_ID_574,GWAS_ID_575,GWAS_ID_576,GWAS_ID_577,GWAS_ID_578,GWAS_ID_579,GWAS_ID_580,GWAS_ID_581,GWAS_ID_582,GWAS_ID_583,GWAS_ID_584,GWAS_ID_585,GWAS_ID_586,GWAS_ID_587,GWAS_ID_588,GWAS_ID_589,GWAS_ID_590,GWAS_ID_591,GWAS_ID_592,GWAS_ID_593,GWAS_ID_594,GWAS_ID_595,GWAS_ID_596,GWAS_ID_597,GWAS_ID_598,GWAS_ID_599,GWAS_ID_600,GWAS_ID_601,GWAS_ID_602,GWAS_ID_603,GWAS_ID_604,GWAS_ID_605,GWAS_ID_606,GWAS_ID_607,GWAS_ID_608,GWAS_ID_609,GWAS_ID_610,GWAS_ID_611,GWAS_ID_612,GWAS_ID_613,GWAS_ID_614,GWAS_ID_615,GWAS_ID_616,GWAS_ID_617,GWAS_ID_618,GWAS_ID_619,GWAS_ID_620 RMVar_hsa_circ_241103,RMVar_hsa_circ_299784,RMVar_hsa_circ_325730,RMVar_hsa_circ_313488,RMVar_hsa_circ_282023,RMVar_hsa_circ_241101,RMVar_hsa_circ_241102 53644 RMVar_ID_53644 Human_SNP_ID_864701734 A-to-I Human chr6 - 157366464 157366464 157366464 AATACTTTTTGGACATTCCTGACTTGGACAATATGATCAAGAAAATGATAAATATTAATATTCTC AATACTTTTTGGACATTCCTGACTTGGACAATGTGATCAAGAAAATGATAAATATTAATATTCTC T C AL390955.1 Ensembl:ENSG00000213078 Pseudogene exon GSE100210 HepG2 cell line chr6:157366463..157366464 29129909 RNA-Seq:(High) rs1336214832 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_22404929 53645 RMVar_ID_53645 Human_SNP_ID_864870224 A-to-I Human chr6 - 29943286 29943286 29943286 GCCCGTCCGACCCCACGTCGCAGCCATACATTATCTGGATGGTGTGAGAACCTGGCCCCGACCCC GCCCGTCCGACCCCACGTCGCAGCCATACATTCTCTGGATGGTGTGAGAACCTGGCCCCGACCCC T G HCG4B,HCG4B:2 RNACentral:URS00009B51D2,RNACentral:URS00008B26E4 lincRNA,lincRNA intron,exon GSE38233 cultured B-cells chr6:29943285..29943286 24183664 RNA-Seq:(High) rs199474485 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,head_neck squamous_cell_carcinoma,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 52 head and neck,haematopoietic and lymphoid tissue 53646 RMVar_ID_53646 Human_SNP_ID_864891300 A-to-I Human chr6 - 57954293 57954293 57954293 TAGGCTCACTGCAACCTCTGCCTCCTGGTTCAAGCAATTTTCCTGCCTCAGCCTCCCCAGTAGCT TAGGCTCACTGCAACCTCTGCCTCCTGGTTCATGCAATTTTCCTGCCTCAGCCTCCCCAGTAGCT T A AL021368.4,LINC00680 Ensembl:ENSG00000283352,Ensembl:ENSG00000215190 lincRNA,Pseudogene intron,intron GSE100210 HepG2 cell line chr6:57954292..57954293 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_17422837 RMVar_hsa_circ_113589,RMVar_hsa_circ_239197,RMVar_hsa_circ_239201,RMVar_hsa_circ_99017 53647 RMVar_ID_53647 Human_SNP_ID_864902488 A-to-I Human chr6 - 158921895 158921895 158921895 GTCTTGCAGGTGACAATGAATGCCCATCCCGGATGGCCTTTACCTTGCTGGAGAAAGTACTAGAT GTCTTGCAGGTGACAATGAATGCCCATCCCGGGTGGCCTTTACCTTGCTGGAGAAAGTACTAGAT T C AL627422.1 Ensembl:ENSG00000213076 Pseudogene exon GSE100210 HepG2 cell line chr6:158921894..158921895 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 1 - 53648 RMVar_ID_53648 Human_SNP_ID_864902521 A-to-I Human chr6 + 27831538 27831538 27831538 CGCCTTTGCCGCGGCCAGACATGACGAGCAAGAGGAGTCTCACCCAACGCTTTGTGAGGACTCTG CGCCTTTGCCGCGGCCAGACATGACGAGCAAGCGGAGTCTCACCCAACGCTTTGTGAGGACTCTG A C RF00017-4544 RNACentral:URS000093B8FA SRP RNA intron GSE100210 HepG2 cell line chr6:27831537..27831538 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 53649 RMVar_ID_53649 Human_SNP_ID_864919596 A-to-I Human chr6 + 72778480 72778480 72778480 GGGGTCGCTTGACCCCCAGAGGAGGGGACTGCAATGAGCAGAGATCACGCCACTGCACTCCAGCC GGGGTCGCTTGACCCCCAGAGGAGGGGACTGCGATGAGCAGAGATCACGCCACTGCACTCCAGCC A G KCNQ5 Ensembl:ENSG00000185760 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank chr6:72778480..72778481 30559470 RNA-Seq:(High) rs1289512610 Functional Loss SNV ICGC 33..33 33 LMS 1 - Human_RBP_ID_23315004 53650 RMVar_ID_53650 Human_SNP_ID_864951806 A-to-I Human chr6 + 43595042 43595042 43595042 TGACATGGTGAAACCCCGTCTCTACAAAAAATACAAATTAGCTGGGCGTGGTGGCATCTGCCTGT TGACATGGTGAAACCCCGTCTCTACAAAAAATGCAAATTAGCTGGGCGTGGTGGCATCTGCCTGT A G POLH Ensembl:ENSG00000170734 Protein coding intron GSE38233 cultured B-cells chr6:43595041..43595042 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_282209,RMVar_hsa_circ_345350,RMVar_hsa_circ_319711,RMVar_hsa_circ_70478,RMVar_hsa_circ_281526,RMVar_hsa_circ_238710,RMVar_hsa_circ_238711,RMVar_hsa_circ_238709 53651 RMVar_ID_53651 Human_SNP_ID_864966568 A-to-I Human chr6 + 142170373 142170373 142170373 TCCAGAAACATGATCAAGTCCTTCTATACTGCAAGTCTTTTGATAGATGTCATAACAGTATTTGG TCCAGAAACATGATCAAGTCCTTCTATACTGCGAGTCTTTTGATAGATGTCATAACAGTATTTGG A G VTA1 Ensembl:ENSG00000009844 Protein coding CDS GSE100210 HepG2 cell line chr6:142170372..142170373 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 stomach adenocarcinoma 4 stomach Human_RBP_ID_950091,Human_RBP_ID_2010057,Human_RBP_ID_9401190,Human_RBP_ID_22462891,Human_RBP_ID_26354445,Human_RBP_ID_27088705,Human_RBP_ID_27828971 Human_Splice_Rec_818306,Human_Splice_Rec_818307,Human_Splice_Rec_818318,Human_Splice_Rec_818319,Human_Splice_Rec_818328,Human_Splice_Rec_818329,Human_Splice_Rec_818342,Human_Splice_Rec_818343,Human_Splice_Rec_818351 Human_miRNA_ID_1247717,Human_miRNA_ID_2721646 RMVar_hsa_circ_95929,RMVar_hsa_circ_241858,RMVar_hsa_circ_277777,RMVar_hsa_circ_336745,RMVar_hsa_circ_359524,RMVar_hsa_circ_277550,RMVar_hsa_circ_241856,RMVar_hsa_circ_241857,RMVar_hsa_circ_241855,RMVar_hsa_circ_85478,RMVar_hsa_circ_241859,RMVar_hsa_circ_241860 53652 RMVar_ID_53652 Human_SNP_ID_864996823 A-to-I Human chr6 - 157366510 157366510 157366510 ATCGGCGTCTTAGTGAACAACGTGGGAATGTCATATGAGTATCCCAAATACTTTTTGGACATTCC ATCGGCGTCTTAGTGAACAACGTGGGAATGTCGTATGAGTATCCCAAATACTTTTTGGACATTCC T C AL390955.1 Ensembl:ENSG00000213078 Pseudogene exon GSE100210 HepG2 cell line chr6:157366509..157366510 29129909 RNA-Seq:(High) rs1436673537 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_26533288 53653 RMVar_ID_53653 Human_SNP_ID_865040159 A-to-I Human chr6 + 29944139 29944139 29944139 GACTCTTCCCGTCAGACCCCCCCAAGACACATATGACCCACCACCCCATCTCTGACCATGAGGCC GACTCTTCCCGTCAGACCCCCCCAAGACACATGTGACCCACCACCCCATCTCTGACCATGAGGCC A G HLA-A Ensembl:ENSG00000206503 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr6:29944138..29944139 30559470 RNA-Seq:(High) rs1425587881 Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 5 large intestine Human_Splice_Rec_747844,Human_Splice_Rec_747858,Human_Splice_Rec_747872,Human_Splice_Rec_747886,Human_Splice_Rec_747898,Human_Splice_Rec_747904,Human_Splice_Rec_747918,Human_Splice_Rec_747926,Human_Splice_Rec_747936 53654 RMVar_ID_53654 Human_SNP_ID_865097962 A-to-I Human chr6 - 148343106 148343106 148343106 GCGGGCTCGGGCTCCGGCTCGGGCTCGGGCTCAGGCTCCGGCCCCGGGCCAGCTGCTCCCGCGTC GCGGGCTCGGGCTCCGGCTCGGGCTCGGGCTCGGGCTCCGGCCCCGGGCCAGCTGCTCCCGCGTC T C - - Other Unknown GSE107867 ASD brains,cerebellum;ASD brains,frontal_cortex;ASD brains,temporal_cortex chr6:148343105..148343106 30559470 RNA-Seq:(High) rs1290001689 Functional Loss SNV ICGC 33..33 33 LMS 1 - 53655 RMVar_ID_53655 Human_SNP_ID_865138533 A-to-I Human chr6 - 165791241 165791241 165791241 AACAGTCAGATTCATAGAATCAAAAAACCTCAAGCTGTCCTCCCACCTTGCCCTTCCAACGCTTC AACAGTCAGATTCATAGAATCAAAAAACCTCATGCTGTCCTCCCACCTTGCCCTTCCAACGCTTC T A PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE100210 HepG2 cell line chr6:165791240..165791241 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_2990116 53656 RMVar_ID_53656 Human_SNP_ID_865207155 A-to-I Human chr6 + 107032289 107032289 107032289 CACATATGCCAAGTGCCTGGCTAGGCCTTGGTAAAACACGCAATTCTTGTCATCAGGGAACTGCC CACATATGCCAAGTGCCTGGCTAGGCCTTGGTGAAACACGCAATTCTTGTCATCAGGGAACTGCC A G MTRES1 Ensembl:ENSG00000130349 Protein coding intron GSE100210 HepG2 cell line chr6:107032288..107032289;chr6:107032289..107032290 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_367028 53657 RMVar_ID_53657 Human_SNP_ID_865211868 A-to-I Human chr6 - 108786187 108786187 108786187 AGGAGGGACCAAGTACAAGAACTGCGTGCATCAGACCAATGAGGTGAAATCTGGAGAAGCAGTAG AGGAGGGACCAAGTACAAGAACTGCGTGCATCTGACCAATGAGGTGAAATCTGGAGAAGCAGTAG T A ZNF259P1 Ensembl:ENSG00000219565 Pseudogene exon GSE100210 HepG2 cell line chr6:108786186..108786187 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - 53658 RMVar_ID_53658 Human_SNP_ID_865307908 A-to-I Human chr6 + 53651538 53651538 53651538 TAAATATTTTCCTTTTCGCGAACTCAGAGGTTAACCACGTGGCTCTACGAATAAATAACGTGTTC TAAATATTTTCCTTTTCGCGAACTCAGAGGTTCACCACGTGGCTCTACGAATAAATAACGTGTTC A C - - Other Unknown GSE100210 HepG2 cell line chr6:53651537..53651538 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - 53659 RMVar_ID_53659 Human_SNP_ID_865322563 A-to-I Human chr6 - 32665264 32665264 32665264 GGCTTTCCTCCCTTTCCTGGATGTAGGAAGGCAGATTCCAGAAGCCCGCAAAGAAGGCGGGCAGA GGCTTTCCTCCCTTTCCTGGATGTAGGAAGGCGGATTCCAGAAGCCCGCAAAGAAGGCGGGCAGA T C HLA-DQB1 Ensembl:ENSG00000179344 Protein coding intron GSE38233 cultured B-cells chr6:32665263..32665264 24183664 RNA-Seq:(High) rs9274428 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 53660 RMVar_ID_53660 Human_SNP_ID_865327953 A-to-I Human chr6 + 42078100 42078100 42078100 TTTAATAGAGATAAGGTTTCGCCATGTTGGCCAGGCTGGTCTTGAACTCCTGACCTCAAGTGATA TTTAATAGAGATAAGGTTTCGCCATGTTGGCCGGGCTGGTCTTGAACTCCTGACCTCAAGTGATA A G TAF8 Ensembl:ENSG00000137413 Protein coding 3'UTR GSE100210 HepG2 cell line chr6:42078099..42078100 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - RMVar_hsa_circ_105984,RMVar_hsa_circ_238347 53661 RMVar_ID_53661 Human_SNP_ID_865378298 A-to-I Human chr6 + 36674899 36674899 36674899 ATCCTCAATGCCACCACCTTAACAGGTGTCATAGATGTAGCTTTGGGGTCAGGTGCCACTGGGGT ATCCTCAATGCCACCACCTTAACAGGTGTCATGGATGTAGCTTTGGGGTCAGGTGCCACTGGGGT A G LAP3P2 Ensembl:ENSG00000213500 Pseudogene exon GSE100210 HepG2 cell line chr6:36674898..36674899 29129909 RNA-Seq:(High) rs1242500366 Functional Loss SNV ICGC 33..33 33 LAML 1 - 53662 RMVar_ID_53662 Human_SNP_ID_865384366 A-to-I Human chr6 - 149724722 149724722 149724722 AAAATTAACCGGGCGTGGTGGCAGGCATCTATAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGA AAAATTAACCGGGCGTGGTGGCAGGCATCTATCATCCCAGCTACTTGGGAGGCTGAGGCAGGAGA T G NUP43 Ensembl:ENSG00000120253 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line chr6:149724721..149724722 29129909,31158229,31158229 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 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 53663 RMVar_ID_53663 Human_SNP_ID_865422413 A-to-I Human chr6 + 25584861 25584861 25584861 ACCTTCCTGCTTTTGCTATTTCCTCAAATGCCAAGGCACCATATTTTGGGGTAGCATGTCCCAAC ACCTTCCTGCTTTTGCTATTTCCTCAAATGCCGAGGCACCATATTTTGGGGTAGCATGTCCCAAC A G CARMIL1 Ensembl:ENSG00000079691 Protein coding intron GSE100210 HepG2 cell line chr6:25584861..25584862 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_7479,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_47078,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_48363,RMVar_hsa_circ_356312 53664 RMVar_ID_53664 Human_SNP_ID_865529267 A-to-I Human chr6 + 42888216 42888216 42888216 TCACCCTGTTGCCCAGGCTGGAGCGCAGTGGCATGATCTCAGCTCATTGCAGCCTCCACCTCCTG TCACCCTGTTGCCCAGGCTGGAGCGCAGTGGCGTGATCTCAGCTCATTGCAGCCTCCACCTCCTG A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr6:42888215..42888216 24183664,29129909 RNA-Seq:(High) rs878875910 Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_252300,Human_RBP_ID_664709 53665 RMVar_ID_53665 Human_SNP_ID_865537387 A-to-I Human chr6 + 42889221 42889221 42889221 TCAACACTTCAGGAGGCTGAGGCAGGCAGATCACTTGAGGTCAGGAGTTCGAGACCAGCCTGACC TCAACACTTCAGGAGGCTGAGGCAGGCAGATCGCTTGAGGTCAGGAGTTCGAGACCAGCCTGACC A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE100210 HepG2 cell line chr6:42889220..42889221 29129909 RNA-Seq:(High) rs1215898569 Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_26829667 Human_miRNA_ID_198594,Human_miRNA_ID_699276,Human_miRNA_ID_704199,Human_miRNA_ID_1288411 53666 RMVar_ID_53666 Human_SNP_ID_865588328 A-to-I Human chr6 + 87240561 87240561 87240561 TCTCCTGCCTCAGCTTCCAAGTAGCTGGGATTACAGGCACCTGCTACCATGCCTGGCTAATTTTG TCTCCTGCCTCAGCTTCCAAGTAGCTGGGATTGCAGGCACCTGCTACCATGCCTGGCTAATTTTG A G ZNF292 Ensembl:ENSG00000188994 Protein coding intron GSE38233 cultured B-cells chr6:87240560..87240561 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_32619,RMVar_hsa_circ_240091,RMVar_hsa_circ_307182,RMVar_hsa_circ_330120,RMVar_hsa_circ_98472,RMVar_hsa_circ_240093,RMVar_hsa_circ_240094,RMVar_hsa_circ_104070,RMVar_hsa_circ_240099,RMVar_hsa_circ_240101,RMVar_hsa_circ_58973,RMVar_hsa_circ_240103 53667 RMVar_ID_53667 Human_SNP_ID_865657199 A-to-I Human chr6 + 71989870 71989870 71989870 TCCTGCATGACCTGGCCTAAGCCTGCTCCTCCAACCCCACCTCAGGCCACACTAACCCTCACTCA TCCTGCATGACCTGGCCTAAGCCTGCTCCTCCTACCCCACCTCAGGCCACACTAACCCTCACTCA A T RIMS1 Ensembl:ENSG00000079841 Protein coding intron GSE107867 ASD brains,cerebellum chr6:71989870..71989871 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_239425,RMVar_hsa_circ_44547,RMVar_hsa_circ_96214,RMVar_hsa_circ_239426 53668 RMVar_ID_53668 Human_SNP_ID_865729571 A-to-I Human chr6 + 36674104 36674104 36674104 GGCAAAGAAAACATCAGAGCTGCTGTTGCAGCAGGATGCAGGCAGATTCAAGACCTGGAGCTCTC GGCAAAGAAAACATCAGAGCTGCTGTTGCAGCGGGATGCAGGCAGATTCAAGACCTGGAGCTCTC A G LAP3P2 Ensembl:ENSG00000213500 Pseudogene exon GSE100210 HepG2 cell line chr6:36674103..36674104 29129909 RNA-Seq:(High) rs878979331 Functional Loss SNV ICGC 33..33 33 LAML 1 - 53669 RMVar_ID_53669 Human_SNP_ID_865771779 A-to-I Human chr6 - 34632325 34632325 34632325 GCTATTCTCTTGCCTCAGCCTCTCTAGTAGCTAGGACTATAGGCGTGTGCCACCACGCTTAACTA GCTATTCTCTTGCCTCAGCCTCTCTAGTAGCTGGGACTATAGGCGTGTGCCACCACGCTTAACTA T C ILRUN Ensembl:ENSG00000196821 Protein coding intron GSE100210 HepG2 cell line chr6:34632324..34632325 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 4 liver RMVar_hsa_circ_79574,RMVar_hsa_circ_82446,RMVar_hsa_circ_237959,RMVar_hsa_circ_237960,RMVar_hsa_circ_237963,RMVar_hsa_circ_359792,RMVar_hsa_circ_271098,RMVar_hsa_circ_237962 53670 RMVar_ID_53670 Human_SNP_ID_865862549 A-to-I Human chr6 - 12311916 12311914 12311916 ATAAAACAGGAGGGCTGGGCATGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGATCGAGGC ATAAAACAGGAGGGCTGGGCATGGTGGCTCAC__CTGTAATCCCAGCACTTTGGGAGATCGAGGC GGT G lnc-ADTRP-7,lnc-ADTRP-7:2,lnc-ADTRP-7:3,lnc-ADTRP-7:4,lnc-ADTRP-7:5,lnc-ADTRP-7:6 RNACentral:URS00008BD3FC,RNACentral:URS0000D5C325,RNACentral:URS00009C1B21,RNACentral:URS00008B360E,RNACentral:URS0000D57B05,RNACentral:URS0000D585E8 lincRNA,lincRNA,lincRNA,lincRNA,lincRNA,lincRNA intron,intron,intron,intron,intron,intron GSE100210 HepG2 cell line chr6:12311915..12311916 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 33..34 33 PAAD 1 - 53671 RMVar_ID_53671 Human_SNP_ID_865906234 A-to-I Human chr6 + 158265516 158265516 158265516 AGCCTGGCCAACATGGTGAAACCCCCGTCCCTACTAAAAGAAAAAAAAAAATTAGCTGGGCGTGA AGCCTGGCCAACATGGTGAAACCCCCGTCCCTGCTAAAAGAAAAAAAAAAATTAGCTGGGCGTGA A G TULP4 Ensembl:ENSG00000130338 Protein coding intron GSE100210 HepG2 cell line chr6:158265515..158265516 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - RMVar_hsa_circ_242666,RMVar_hsa_circ_242665 53672 RMVar_ID_53672 Human_SNP_ID_865993637 A-to-I Human chr6 + 33398501 33398501 33398501 ATTTTATTTTTTTTGAGACAGAGTCTCGCTCTATCGCCCAGGCTGGAGTGCAGTGGCTCAATCTC ATTTTATTTTTTTTGAGACAGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCTCAATCTC A G KIFC1 Ensembl:ENSG00000237649 Protein coding intron GSE38233 cultured B-cells chr6:33398500..33398501 24183664 RNA-Seq:(High) rs1331844568 Functional Loss SNV COSMIC 33..33 33 rectum adenocarcinoma,large_intestine adenocarcinoma 1 large intestine Human_miRNA_ID_2972951,Human_miRNA_ID_3006135 RMVar_hsa_circ_107733,RMVar_hsa_circ_237859 53673 RMVar_ID_53673 Human_SNP_ID_865994227 A-to-I Human chr6 - 89725775 89725775 89725775 CCCGGGAGTTTGAGACCATCCTGGACAACATAACAAGACCTTGGCTCTACCAAAAAAAAAAAAAA CCCGGGAGTTTGAGACCATCCTGGACAACATAGCAAGACCTTGGCTCTACCAAAAAAAAAAAAAA T C MDN1 Ensembl:ENSG00000112159 Protein coding intron GSE100210 HepG2 cell line chr6:89725774..89725775 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_95989,RMVar_hsa_circ_125853,RMVar_hsa_circ_240243,RMVar_hsa_circ_240245,RMVar_hsa_circ_240244,RMVar_hsa_circ_107596,RMVar_hsa_circ_240254,RMVar_hsa_circ_77464,RMVar_hsa_circ_265022,RMVar_hsa_circ_269189,RMVar_hsa_circ_240260,RMVar_hsa_circ_116956,RMVar_hsa_circ_117784,RMVar_hsa_circ_96630,RMVar_hsa_circ_114984,RMVar_hsa_circ_240262,RMVar_hsa_circ_93682,RMVar_hsa_circ_240263,RMVar_hsa_circ_240261,RMVar_hsa_circ_76756,RMVar_hsa_circ_240259,RMVar_hsa_circ_76109,RMVar_hsa_circ_240265,RMVar_hsa_circ_240266,RMVar_hsa_circ_25965,RMVar_hsa_circ_58449,RMVar_hsa_circ_87333,RMVar_hsa_circ_123487,RMVar_hsa_circ_51774,RMVar_hsa_circ_73013,RMVar_hsa_circ_79291,RMVar_hsa_circ_240269,RMVar_hsa_circ_25824,RMVar_hsa_circ_240268,RMVar_hsa_circ_108649,RMVar_hsa_circ_240272,RMVar_hsa_circ_240273,RMVar_hsa_circ_100109,RMVar_hsa_circ_269119,RMVar_hsa_circ_76398,RMVar_hsa_circ_240275,RMVar_hsa_circ_116655,RMVar_hsa_circ_125139,RMVar_hsa_circ_240277,RMVar_hsa_circ_240281,RMVar_hsa_circ_240280,RMVar_hsa_circ_240282,RMVar_hsa_circ_103726,RMVar_hsa_circ_266447,RMVar_hsa_circ_42388,RMVar_hsa_circ_65304,RMVar_hsa_circ_240283,RMVar_hsa_circ_120459,RMVar_hsa_circ_355211,RMVar_hsa_circ_368760,RMVar_hsa_circ_111135,RMVar_hsa_circ_118841,RMVar_hsa_circ_99087,RMVar_hsa_circ_240286,RMVar_hsa_circ_240287,RMVar_hsa_circ_240288,RMVar_hsa_circ_55432,RMVar_hsa_circ_353298,RMVar_hsa_circ_34051 53674 RMVar_ID_53674 Human_SNP_ID_866006822 A-to-I Human chr6 - 5256086 5256086 5256086 CTAATTTTCTCACCTTAAACTAGGATTTCTCAATCTTGGCATGACCAACCTTTTGGGCCAGCTAA CTAATTTTCTCACCTTAAACTAGGATTTCTCAGTCTTGGCATGACCAACCTTTTGGGCCAGCTAA T C LYRM4 Ensembl:ENSG00000214113 Protein coding intron GSE100210 HepG2 cell line chr6:5256085..5256086 29129909 RNA-Seq:(High) rs1266464039 Functional Loss SNV ICGC 33..33 33 STAD 1 - 53675 RMVar_ID_53675 Human_SNP_ID_866026789 A-to-I Human chr6 - 136636698 136636698 136636698 GCTCAAGCAATCCTCCCACCTCGGCCTCCCAAAGCACTAGAATTACAGGCGTGAGCCACCGCACC GCTCAAGCAATCCTCCCACCTCGGCCTCCCAAGGCACTAGAATTACAGGCGTGAGCCACCGCACC T C MAP3K5 Ensembl:ENSG00000197442 Protein coding intron GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line chr6:136636697..136636698 32596459 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_8182,RMVar_hsa_circ_87272,RMVar_hsa_circ_241710,RMVar_hsa_circ_126061,RMVar_hsa_circ_241711,RMVar_hsa_circ_66632,RMVar_hsa_circ_371758,RMVar_hsa_circ_267793,RMVar_hsa_circ_241716,RMVar_hsa_circ_4763,RMVar_hsa_circ_102899,RMVar_hsa_circ_38131,RMVar_hsa_circ_104208,RMVar_hsa_circ_241719,RMVar_hsa_circ_321104,RMVar_hsa_circ_241721,RMVar_hsa_circ_47510,RMVar_hsa_circ_39793,RMVar_hsa_circ_313431,RMVar_hsa_circ_67118,RMVar_hsa_circ_241722,RMVar_hsa_circ_121711,RMVar_hsa_circ_241724,RMVar_hsa_circ_241727,RMVar_hsa_circ_327672,RMVar_hsa_circ_82073,RMVar_hsa_circ_265852,RMVar_hsa_circ_241725,RMVar_hsa_circ_377769,RMVar_hsa_circ_70722,RMVar_hsa_circ_277617,RMVar_hsa_circ_32055,RMVar_hsa_circ_241726 53676 RMVar_ID_53676 Human_SNP_ID_866159494 A-to-I Human chr6 + 42889285 42889285 42889285 CAACATGGAGAAATTCTGTCCCTACTGAAAATACAAAATTAGCCGGATGTGGTGGTGCATGCCTG CAACATGGAGAAATTCTGTCCCTACTGAAAATGCAAAATTAGCCGGATGTGGTGGTGCATGCCTG A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr6:42889284..42889285 24183664,29129909 RNA-Seq:(High) rs1134326 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_26540170 53677 RMVar_ID_53677 Human_SNP_ID_866162409 A-to-I Human chr6 - 158777698 158777698 158777698 GTCCACCCCACTGCCTTGATCTAGTTGATGTGATCATAACGAAACCTGTATTGCTCATCAGTATT GTCCACCCCACTGCCTTGATCTAGTTGATGTGGTCATAACGAAACCTGTATTGCTCATCAGTATT T C EZR Ensembl:ENSG00000092820 Protein coding intron GSE38233 cultured B-cells chr6:158777697..158777698 24183664 RNA-Seq:(High) rs3102971 Functional Loss SNV ICGC 33..33 33 ESCA 1 - GWAS_ID_5118,GWAS_ID_5119,GWAS_ID_5120 RMVar_hsa_circ_242772,RMVar_hsa_circ_86438,RMVar_hsa_circ_107253,RMVar_hsa_circ_125699,RMVar_hsa_circ_117290,RMVar_hsa_circ_91261,RMVar_hsa_circ_242776,RMVar_hsa_circ_83509,RMVar_hsa_circ_242774,RMVar_hsa_circ_242775,RMVar_hsa_circ_242773,RMVar_hsa_circ_124652,RMVar_hsa_circ_242771,RMVar_hsa_circ_295008,RMVar_hsa_circ_242783,RMVar_hsa_circ_364284,RMVar_hsa_circ_267771,RMVar_hsa_circ_323222,RMVar_hsa_circ_242785,RMVar_hsa_circ_242786 53678 RMVar_ID_53678 Human_SNP_ID_866247482 A-to-I Human chr6 - 29829459 29829459 29829459 GCCCAGGGCCCAGCACCTCAGGGTGGCCTCATAGTCAAAGACAGGGTGGTGGGTCACGTGTGTCT GCCCAGGGCCCAGCACCTCAGGGTGGCCTCATGGTCAAAGACAGGGTGGTGGGTCACGTGTGTCT T C - - Other Unknown GSE100210 HepG2 cell line chr6:29829458..29829459 29129909 RNA-Seq:(High) rs1285867439 Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma 10 haematopoietic and lymphoid tissue 53679 RMVar_ID_53679 Human_SNP_ID_866247966 A-to-I Human chr6 + 27737943 27737943 27737943 GATCCCATGTTTTGGGCTGAGAATGGGAAAGGAATCTCCTAGTTTCCAGAAAAAACAGATAAAGG GATCCCATGTTTTGGGCTGAGAATGGGAAAGGGATCTCCTAGTTTCCAGAAAAAACAGATAAAGG A G RF00017-4544 RNACentral:URS000093B8FA SRP RNA intron GSE100210 HepG2 cell line chr6:27737942..27737943 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 1 - 53680 RMVar_ID_53680 Human_SNP_ID_866289097 A-to-I Human chr6 + 144200905 144200905 144200905 CACCTCCAGGTACAGCCCGTCCATGATCTCCCAGATCTTGTAGATGTCGGAAAACATCTCATCGT CACCTCCAGGTACAGCCCGTCCATGATCTCCCGGATCTTGTAGATGTCGGAAAACATCTCATCGT A G - - Other Unknown GSE100210 HepG2 cell line chr6:144200904..144200905 29129909 RNA-Seq:(High) rs567622531 Functional Loss SNV ICGC 33..33 33 PBCA 1 - 53681 RMVar_ID_53681 Human_SNP_ID_866312646 A-to-I Human chr6 - 108042419 108042419 108042419 AGAGCCAGACCTTGTCTCAAAAAAAAAAAAAAAAAAAGAAAAAAGAAAGTACTGTCTGTCTTAAA AGAGCCAGACCTTGTCTCAAAAAAAAAAAAAAGAAAAGAAAAAAGAAAGTACTGTCTGTCTTAAA T C OSTM1 Ensembl:ENSG00000081087 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line chr6:108042418..108042419 31158229 RNA-Seq:(High) rs564822548 Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 2 ovary Human_RBP_ID_25949725 RMVar_hsa_circ_265883 53682 RMVar_ID_53682 Human_SNP_ID_866316897 A-to-I Human chr6 + 100889581 100889581 100889581 TTGGACACATCGCCGCTTCTAGACCCTCCTGCAGTCTCGGATATTGCTGGGAAAATGTCTGATGA TTGGACACATCGCCGCTTCTAGACCCTCCTGCGGTCTCGGATATTGCTGGGAAAATGTCTGATGA A G - - Other Unknown GSE38233 cultured B-cells chr6:100889580..100889581 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 1 - 53683 RMVar_ID_53683 Human_SNP_ID_866439646 A-to-I Human chr6 + 149804770 149804770 149804770 GTGATCTGCCCGCCTCGGCCTCCCAAAGTGCTAGGATTACAGGTGTCAGCCACCATGCCTGGCCC GTGATCTGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTCAGCCACCATGCCTGGCCC A G PCMT1 Ensembl:ENSG00000120265 Protein coding intron GSE100210 HepG2 cell line chr6:149804769..149804770 29129909 RNA-Seq:(High) rs929455489 Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 4 prostate RMVar_hsa_circ_88233,RMVar_hsa_circ_91931,RMVar_hsa_circ_242254,RMVar_hsa_circ_82745,RMVar_hsa_circ_242265,RMVar_hsa_circ_242269 53684 RMVar_ID_53684 Human_SNP_ID_866448048 A-to-I Human chr6 + 69112955 69112955 69112955 GCTTTTTGTATTTTCAGTAGAGATGGGGTTTCACCATCTTGGCCAGACTGGTCTAGAACTCCTGA GCTTTTTGTATTTTCAGTAGAGATGGGGTTTCGCCATCTTGGCCAGACTGGTCTAGAACTCCTGA A G ADGRB3 Ensembl:ENSG00000135298 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank chr6:69112954..69112955 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_3089,RMVar_hsa_circ_321446,RMVar_hsa_circ_307700,RMVar_hsa_circ_45501,RMVar_hsa_circ_99653,RMVar_hsa_circ_11186,RMVar_hsa_circ_239305,RMVar_hsa_circ_37219,RMVar_hsa_circ_239279,RMVar_hsa_circ_239280,RMVar_hsa_circ_84780,RMVar_hsa_circ_94199,RMVar_hsa_circ_239306,RMVar_hsa_circ_26808,RMVar_hsa_circ_340693,RMVar_hsa_circ_239318,RMVar_hsa_circ_304759,RMVar_hsa_circ_335648,RMVar_hsa_circ_279422 53685 RMVar_ID_53685 Human_SNP_ID_866448290 A-to-I Human chr6 + 138650369 138650369 138650369 GGGGAGTAACGGGGGAGCCCAGCCTGCAGCCCACAGTTGTTCACAGCCATGAGGTCGCCGACTAG GGGGAGTAACGGGGGAGCCCAGCCTGCAGCCCGCAGTTGTTCACAGCCATGAGGTCGCCGACTAG A G - - Other Unknown GSE100210 HepG2 cell line chr6:138650368..138650369 29129909 RNA-Seq:(High) rs888909254 Functional Loss SNV ICGC 33..33 33 LAML 1 - 53686 RMVar_ID_53686 Human_SNP_ID_866456784 A-to-I Human chr6 - 97279703 97279703 97279703 TGGCTCACTGCAACTTCCGCCTCCCGAGTTTAAGCGCTTCTTTGCCTCAGCTTCCCGAGTAGCTC TGGCTCACTGCAACTTCCGCCTCCCGAGTTTAGGCGCTTCTTTGCCTCAGCTTCCCGAGTAGCTC T C MMS22L Ensembl:ENSG00000146263 Protein coding intron GSE100210 HepG2 cell line chr6:97279702..97279703 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 3 liver Human_RBP_ID_15917948,Human_RBP_ID_18084297 RMVar_hsa_circ_340780,RMVar_hsa_circ_45643,RMVar_hsa_circ_22819,RMVar_hsa_circ_45744,RMVar_hsa_circ_109190,RMVar_hsa_circ_48155,RMVar_hsa_circ_92115,RMVar_hsa_circ_240414,RMVar_hsa_circ_240415 53687 RMVar_ID_53687 Human_SNP_ID_866459286 A-to-I Human chr6 + 42889185 42889185 42889185 AGCTTAGGCTGGGCACGGTGGCTCACACCTGTAATCTCAACACTTCAGGAGGCTGAGGCAGGCAG AGCTTAGGCTGGGCACGGTGGCTCACACCTGTGATCTCAACACTTCAGGAGGCTGAGGCAGGCAG A G RPL7L1 Ensembl:ENSG00000146223 Protein coding 3'UTR GSE38233;GSE100210;GSE100210 cultured B-cells;HepG2 cell line;HepG2 cell line chr6:42889184..42889185;chr6:42889185..42889186 24183664,29129909,29129909 RNA-Seq:(High) rs1562515264 Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_18084883,Human_RBP_ID_26536833 53688 RMVar_ID_53688 Human_SNP_ID_866526207 A-to-I Human chr6 - 71410035 71410035 71410035 AGATTTTTTTTTTTCTTTTTTTGAGTCAGGTTATCTCTGTCGCTCAAGCTGGAGTTCAGTGGCAT AGATTTTTTTTTTTCTTTTTTTGAGTCAGGTTGTCTCTGTCGCTCAAGCTGGAGTTCAGTGGCAT T C LINC00472,AL136164.2 Ensembl:ENSG00000233237,Ensembl:ENSG00000269966 lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line chr6:71410034..71410035 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_3016775,Human_RBP_ID_10294092,Human_RBP_ID_15941658 53689 RMVar_ID_53689 Human_SNP_ID_866553836 A-to-I Human chr6 + 43137946 43137946 43137946 CTTGTGCCTCAGCCTCCCCAGTAGCTGGGATTACAGGTGCCCGCCACCACACCCGGCCAATGTTT CTTGTGCCTCAGCCTCCCCAGTAGCTGGGATTGCAGGTGCCCGCCACCACACCCGGCCAATGTTT A G PTK7 Ensembl:ENSG00000112655 Protein coding intron GSE100210 HepG2 cell line chr6:43137945..43137946 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - 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_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 53690 RMVar_ID_53690 Human_SNP_ID_866565156 A-to-I Human chr6 - 31803859 31803859 31803859 TATGTACATTTAGGCCAGATGCGGTGGCTCATACCTGTAATCCCAGCACTTTGGGAAGTCGAGGC TATGTACATTTAGGCCAGATGCGGTGGCTCATCCCTGTAATCCCAGCACTTTGGGAAGTCGAGGC T G LSM2 Ensembl:ENSG00000204392 Protein coding intron GSE100210 HepG2 cell line chr6:31803858..31803859 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 53691 RMVar_ID_53691 Human_SNP_ID_866566815 A-to-I Human chr6 - 85735734 85735734 85735734 AATCAGAGAAAAAAGATAACTGAATATTCTGCAATGTAAATGTCAGCTTGAGTGGACTCCGGCTG AATCAGAGAAAAAAGATAACTGAATATTCTGCCATGTAAATGTCAGCTTGAGTGGACTCCGGCTG T G L13712-001 RNACentral:URS0000334622 misc_RNA intron GSE38233 cultured B-cells chr6:85735733..85735734 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 2 - 53692 RMVar_ID_53692 Human_SNP_ID_866602161 A-to-I Human chr6 + 36457450 36457450 36457450 AATGTTGAGGCCGGGTACGGGGACTCACGCCTATAATTCCAATGCTTTGGGAGGCCCAGGTGGGA AATGTTGAGGCCGGGTACGGGGACTCACGCCTGTAATTCCAATGCTTTGGGAGGCCCAGGTGGGA A G KCTD20 Ensembl:ENSG00000112078 Protein coding intron GSE38233 cultured B-cells chr6:36457449..36457450 24183664 RNA-Seq:(High) rs76019396 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_22482641 GWAS_ID_1726,GWAS_ID_1727,GWAS_ID_1728,GWAS_ID_1729,GWAS_ID_1730,GWAS_ID_1731,GWAS_ID_1732,GWAS_ID_1733,GWAS_ID_1734,GWAS_ID_1735,GWAS_ID_1736,GWAS_ID_1737,GWAS_ID_1738 RMVar_hsa_circ_238130 53693 RMVar_ID_53693 Human_SNP_ID_866628054 A-to-I Human chr6 + 107041009 107041009 107041009 AGCACTTTGGGAGGCCAAGGCGGGCGGATCACAAGGTCAGGAGATCGAGACCATCCTGGCTAGCA AGCACTTTGGGAGGCCAAGGCGGGCGGATCACGAGGTCAGGAGATCGAGACCATCCTGGCTAGCA A G MTRES1 Ensembl:ENSG00000130349 Protein coding intron GSE38233 cultured B-cells chr6:107041009..107041010 24183664 RNA-Seq:(High) rs62429963 Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_240701,RMVar_hsa_circ_367028,RMVar_hsa_circ_300689 53694 RMVar_ID_53694 Human_SNP_ID_866673813 A-to-I Human chr6 - 138546346 138546331 138546346 GCTCAAGTGATATTCCCACCTTGGTCTCCCAAAGTTCTGGGATTATAGGTGTGAGCCACCATGTC GCTCAAGTGATATTCCCACCTTGGTCTCCCAA_______________GGTGTGAGCCACCATGTC CTATAATCCCAGAACT C NHSL1 Ensembl:ENSG00000135540 Protein coding intron GSE100210 HepG2 cell line chr6:138546345..138546346 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 33..47 33 PAAD 1 - RMVar_hsa_circ_241802,RMVar_hsa_circ_241807,RMVar_hsa_circ_96629 53695 RMVar_ID_53695 Human_SNP_ID_866689630 A-to-I Human chr6 - 7517011 7517011 7517011 GCCTGTAAAAACTATGATGGTGACATGCAGTCAGACTCTGTGGCCCAAGGGTATGGCTCTCTTGG GCCTGTAAAAACTATGATGGTGACATGCAGTCGGACTCTGTGGCCCAAGGGTATGGCTCTCTTGG T C AL138878.2 Ensembl:ENSG00000234115 Pseudogene exon GSE100210 HepG2 cell line chr6:7517010..7517011 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 1 - 53696 RMVar_ID_53696 Human_SNP_ID_866696344 A-to-I Human chr6 - 131185033 131185033 131185033 CTGGGCAAGTTTCCTGTGACAAACAGTCAAGCACGAAAGCGGATCCTAGAACCAGATGACTTCCT CTGGGCAAGTTTCCTGTGACAAACAGTCAAGCGCGAAAGCGGATCCTAGAACCAGATGACTTCCT T C AL137222.1 Ensembl:ENSG00000218857 Pseudogene exon GSE100210 HepG2 cell line chr6:131185032..131185033 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue 53697 RMVar_ID_53697 Human_SNP_ID_866717484 A-to-I Human chr6 - 166982385 166982385 166982385 AGAGTGAAACTCCGTCTCAAAAAAAAAAAAAAAAAAAAGAAAATCAAAAGGAATAGATCCAAACA AGAGTGAAACTCCGTCTCAAAAAAAAAAAAAAGAAAAAGAAAATCAAAAGGAATAGATCCAAACA T C Z94721.1 Ensembl:ENSG00000227598 lincRNA intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line chr6:166982384..166982385 31158229 RNA-Seq:(High) rs370876914 Functional Loss SNV ICGC 33..33 33 COCA 1 - GWAS_ID_4170,GWAS_ID_4171,GWAS_ID_4172,GWAS_ID_4173,GWAS_ID_4174,GWAS_ID_4175,GWAS_ID_4176,GWAS_ID_4177,GWAS_ID_4178,GWAS_ID_4179,GWAS_ID_4180,GWAS_ID_4181,GWAS_ID_4182,GWAS_ID_4183,GWAS_ID_4184,GWAS_ID_4185,GWAS_ID_4186,GWAS_ID_4187,GWAS_ID_4188,GWAS_ID_4189,GWAS_ID_4190,GWAS_ID_4191,GWAS_ID_4192,GWAS_ID_4193,GWAS_ID_4194,GWAS_ID_4195,GWAS_ID_4196,GWAS_ID_4197,GWAS_ID_4198,GWAS_ID_4199,GWAS_ID_4200,GWAS_ID_4201,GWAS_ID_4202,GWAS_ID_4203,GWAS_ID_4204,GWAS_ID_4205,GWAS_ID_4206,GWAS_ID_4207,GWAS_ID_4208,GWAS_ID_4209,GWAS_ID_4210,GWAS_ID_4211,GWAS_ID_4212,GWAS_ID_4213,GWAS_ID_4214,GWAS_ID_4215,GWAS_ID_4216,GWAS_ID_4217,GWAS_ID_4218,GWAS_ID_4219,GWAS_ID_4220,GWAS_ID_4221,GWAS_ID_4222,GWAS_ID_4223,GWAS_ID_4224,GWAS_ID_4225,GWAS_ID_4226,GWAS_ID_4227,GWAS_ID_4228,GWAS_ID_4229,GWAS_ID_4230,GWAS_ID_4231,GWAS_ID_4232,GWAS_ID_4233,GWAS_ID_4234,GWAS_ID_4235,GWAS_ID_4236,GWAS_ID_4237,GWAS_ID_4238,GWAS_ID_4239,GWAS_ID_4240,GWAS_ID_4241,GWAS_ID_4242,GWAS_ID_4243,GWAS_ID_4244,GWAS_ID_4245,GWAS_ID_4246,GWAS_ID_4247,GWAS_ID_4248,GWAS_ID_4249,GWAS_ID_4250,GWAS_ID_4251,GWAS_ID_4252,GWAS_ID_4253,GWAS_ID_4254,GWAS_ID_4255,GWAS_ID_4256,GWAS_ID_4257,GWAS_ID_4258,GWAS_ID_4259,GWAS_ID_4260,GWAS_ID_4261,GWAS_ID_4262,GWAS_ID_4263,GWAS_ID_4264,GWAS_ID_4265,GWAS_ID_4266,GWAS_ID_4267,GWAS_ID_4268,GWAS_ID_4269,GWAS_ID_4270,GWAS_ID_4271,GWAS_ID_4272,GWAS_ID_4273,GWAS_ID_4274,GWAS_ID_4275,GWAS_ID_4276,GWAS_ID_4277,GWAS_ID_4278,GWAS_ID_4279,GWAS_ID_4280,GWAS_ID_4281,GWAS_ID_4282,GWAS_ID_4283,GWAS_ID_4284,GWAS_ID_4285,GWAS_ID_4286,GWAS_ID_4287,GWAS_ID_4288,GWAS_ID_4289,GWAS_ID_4290,GWAS_ID_4291,GWAS_ID_4292,GWAS_ID_4293,GWAS_ID_4294,GWAS_ID_4295,GWAS_ID_4296,GWAS_ID_4297,GWAS_ID_4298,GWAS_ID_4299,GWAS_ID_4300,GWAS_ID_4301,GWAS_ID_4302,GWAS_ID_4303,GWAS_ID_4304,GWAS_ID_4305,GWAS_ID_4306,GWAS_ID_4307,GWAS_ID_4308,GWAS_ID_4309,GWAS_ID_4310,GWAS_ID_4311,GWAS_ID_4312,GWAS_ID_4313,GWAS_ID_4314,GWAS_ID_4315,GWAS_ID_4316,GWAS_ID_4317,GWAS_ID_4318,GWAS_ID_4319 53698 RMVar_ID_53698 Human_SNP_ID_866837401 A-to-I Human chr6 - 158921844 158921844 158921844 AGAAAGTACTAGATGAATTCTCCAAGCAAGTCAACAGGATAGACTGGCCAGAAGGATCCCCTGCT AGAAAGTACTAGATGAATTCTCCAAGCAAGTCGACAGGATAGACTGGCCAGAAGGATCCCCTGCT T C AL627422.1 Ensembl:ENSG00000213076 Pseudogene exon GSE100210 HepG2 cell line chr6:158921843..158921844 29129909 RNA-Seq:(High) rs1049509131 Functional Loss SNV ICGC 33..33 33 LAML 1 - 53699 RMVar_ID_53699 Human_SNP_ID_866877766 A-to-I Human chr6 + 35300058 35300058 35300058 TTGTTGTTGTTTTAGAGATGAGATCTTGTTCTATCACTCATGCTGGAGTGCAGTGGTGCAGTCAT TTGTTGTTGTTTTAGAGATGAGATCTTGTTCTGTCACTCATGCTGGAGTGCAGTGGTGCAGTCAT A G DEF6 Ensembl:ENSG00000023892 Protein coding intron GSE38233 cultured B-cells chr6:35300057..35300058 24183664 RNA-Seq:(High) rs563132099 Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 2 prostate RMVar_hsa_circ_110847,RMVar_hsa_circ_238039,RMVar_hsa_circ_93192,RMVar_hsa_circ_238040 53700 RMVar_ID_53700 Human_SNP_ID_866897590 A-to-I Human chr6 - 165897468 165897468 165897468 GGGACCTCACTCCCTGGGGGCACCTGCAGCTCAGGACCCTCTCATTCTCCTCCCTGGGACCCTCC GGGACCTCACTCCCTGGGGGCACCTGCAGCTCCGGACCCTCTCATTCTCCTCCCTGGGACCCTCC T G PDE10A Ensembl:ENSG00000112541 Protein coding intron GSE100210 HepG2 cell line chr6:165897467..165897468 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - 53701 RMVar_ID_53701 Human_SNP_ID_866898922 A-to-I Human chr6 + 42785546 42785532 42785546 CCCCACCATTGCACTCCAGTCCGGGAAACAAGAACGAAACTCCCATCTCAAAAAAAAAAAAAAGA CCCCACCATTGCACTCCAG______________ACGAAACTCCCATCTCAAAAAAAAAAAAAAGA GTCCGGGAAACAAGA G BICRAL Ensembl:ENSG00000112624 Protein coding intron GSE100210 HepG2 cell line chr6:42785546..42785547 29129909 RNA-Seq:(High) rs552902992 Functional Loss DEL ICGC 20..33 33 ESCA 1 - 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 53702 RMVar_ID_53702 Human_SNP_ID_866916967 A-to-I Human chr6 - 31538320 31538320 31538320 GAAACCCTCTCTCTACTAAAAATGCAAAAATTAGCCGTGCATGGTGGCACACACCTATAGTCCCA GAAACCCTCTCTCTACTAAAAATGCAAAAATTTGCCGTGCATGGTGGCACACACCTATAGTCCCA T A DDX39B,ATP6V1G2-DDX39B Ensembl:ENSG00000198563,Ensembl:ENSG00000254870 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells chr6:31538319..31538320 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_15785987 53703 RMVar_ID_53703 Human_SNP_ID_866942737 A-to-I Human chr6 - 158921872 158921872 158921872 CCATCCCGGATGGCCTTTACCTTGCTGGAGAAAGTACTAGATGAATTCTCCAAGCAAGTCAACAG CCATCCCGGATGGCCTTTACCTTGCTGGAGAAGGTACTAGATGAATTCTCCAAGCAAGTCAACAG T C AL627422.1 Ensembl:ENSG00000213076 Pseudogene exon GSE100210 HepG2 cell line chr6:158921871..158921872 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 1 - 53704 RMVar_ID_53704 Human_SNP_ID_866985965 A-to-I Human chr6 - 1652160 1652160 1652160 ACCATGTTGGCCAGGCTGGTCTCGAACTCTTGACCTCAGATGATCCACCCGCCTCGCCTCCCAAA ACCATGTTGGCCAGGCTGGTCTCGAACTCTTGCCCTCAGATGATCCACCCGCCTCGCCTCCCAAA T G GMDS Ensembl:ENSG00000112699 Protein coding intron GSE100210 HepG2 cell line chr6:1652159..1652160 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BOCA 1 - 53705 RMVar_ID_53705 Human_SNP_ID_867015735 A-to-I Human chr6 - 134942028 134942028 134942028 TTAGTAGAAACAGGGTTTCACCCATGTTGGCCAGGCTGATCTCAAACTCCTGACCTCAAGTTATC TTAGTAGAAACAGGGTTTCACCCATGTTGGCCGGGCTGATCTCAAACTCCTGACCTCAAGTTATC T C ALDH8A1 Ensembl:ENSG00000118514 Protein coding intron GSE100210 HepG2 cell line chr6:134942027..134942028 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_72237,RMVar_hsa_circ_241606,RMVar_hsa_circ_309133 53706 RMVar_ID_53706 Human_SNP_ID_867056082 A-to-I Human chr6 - 7517019 7517019 7517019 TCATCTGGGCCTGTAAAAACTATGATGGTGACATGCAGTCAGACTCTGTGGCCCAAGGGTATGGC TCATCTGGGCCTGTAAAAACTATGATGGTGACGTGCAGTCAGACTCTGTGGCCCAAGGGTATGGC T C AL138878.2 Ensembl:ENSG00000234115 Pseudogene exon GSE100210 HepG2 cell line chr6:7517018..7517019 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_miRNA_ID_1842635,Human_miRNA_ID_1905203 53707 RMVar_ID_53707 Human_SNP_ID_867057541 A-to-I Human chr6 - 26056064 26056063 26056064 AGCCTCCGGGGAAGCCAAGCCCAAGGTTAAAAAGGCGGGCGGAACCAAACCTAAGAAGCCAGTTG AGCCTCCGGGGAAGCCAAGCCCAAGGTTAAAA_GGCGGGCGGAACCAAACCTAAGAAGCCAGTTG CT C H1-2 Ensembl:ENSG00000187837 Protein coding CDS GSE100210 HepG2 cell line chr6:26056063..26056064 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 33..33 33 CLLE 1 - Human_RBP_ID_658977,Human_RBP_ID_1045983,Human_RBP_ID_1216573,Human_RBP_ID_1668818,Human_RBP_ID_2016674,Human_RBP_ID_4876069,Human_RBP_ID_8141006,Human_RBP_ID_8899074,Human_RBP_ID_9192811,Human_RBP_ID_15769998,Human_RBP_ID_17305953,Human_RBP_ID_17419185,Human_RBP_ID_18071316,Human_RBP_ID_18202478,Human_RBP_ID_18449930,Human_RBP_ID_18860535,Human_RBP_ID_22102274,Human_RBP_ID_22460428,Human_RBP_ID_22772629,Human_RBP_ID_22830329,Human_RBP_ID_23137892,Human_RBP_ID_26353470,Human_RBP_ID_26534353,Human_RBP_ID_26829091,Human_RBP_ID_27093640,Human_RBP_ID_27521851 RMVar_hsa_circ_237733,RMVar_hsa_circ_237735,RMVar_hsa_circ_377187,RMVar_hsa_circ_266433 53708 RMVar_ID_53708 Human_SNP_ID_834033526 A-to-I Human chr2 - 60735361 60735361 60735361 TTTCTAAAACCATATACTTTAGAAGAACAGAAAAACCTCACAGTCTGTCCTGATGGAGCACTTTT TTTCTAAAACCATATACTTTAGAAGAACAGAAGAACCTCACAGTCTGTCCTGATGGAGCACTTTT T C ATP1B3P1 Ensembl:ENSG00000271707 Pseudogene exon GSE100210 HepG2 cell line chr2:60735360..60735361 29129909 RNA-Seq:(High) rs879188828 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_5590686,Human_RBP_ID_8258007,Human_RBP_ID_18533676 Human_miRNA_ID_1823096,Human_miRNA_ID_1874344,Human_miRNA_ID_1878007,Human_miRNA_ID_1883580 53709 RMVar_ID_53709 Human_SNP_ID_834037513 A-to-I Human chr2 - 43920411 43920411 43920411 TAGGCTGCAGCTGGGCAAGGTGGCTCACACCTATAATCCCAGCACTTTGGGAGGCCAAGGCCAGT TAGGCTGCAGCTGGGCAAGGTGGCTCACACCTTTAATCCCAGCACTTTGGGAGGCCAAGGCCAGT T A LRPPRC Ensembl:ENSG00000138095 Protein coding intron GSE100210 HepG2 cell line chr2:43920410..43920411 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_6922457,Human_RBP_ID_13892300 RMVar_hsa_circ_2968,RMVar_hsa_circ_628,RMVar_hsa_circ_23322,RMVar_hsa_circ_57044,RMVar_hsa_circ_267196,RMVar_hsa_circ_42731,RMVar_hsa_circ_33116,RMVar_hsa_circ_121609,RMVar_hsa_circ_334855,RMVar_hsa_circ_56178,RMVar_hsa_circ_308772,RMVar_hsa_circ_199381,RMVar_hsa_circ_199382,RMVar_hsa_circ_59979,RMVar_hsa_circ_305149,RMVar_hsa_circ_199383,RMVar_hsa_circ_25563,RMVar_hsa_circ_341074,RMVar_hsa_circ_365415,RMVar_hsa_circ_313240,RMVar_hsa_circ_65860,RMVar_hsa_circ_78179,RMVar_hsa_circ_42425,RMVar_hsa_circ_199391,RMVar_hsa_circ_340645,RMVar_hsa_circ_114021,RMVar_hsa_circ_199385,RMVar_hsa_circ_199387,RMVar_hsa_circ_199388,RMVar_hsa_circ_199386,RMVar_hsa_circ_268053,RMVar_hsa_circ_355943,RMVar_hsa_circ_373562,RMVar_hsa_circ_375386,RMVar_hsa_circ_199389,RMVar_hsa_circ_374357,RMVar_hsa_circ_368467,RMVar_hsa_circ_342103,RMVar_hsa_circ_21576,RMVar_hsa_circ_273864,RMVar_hsa_circ_199393,RMVar_hsa_circ_199395,RMVar_hsa_circ_199394,RMVar_hsa_circ_199392,RMVar_hsa_circ_19510,RMVar_hsa_circ_283018,RMVar_hsa_circ_341842,RMVar_hsa_circ_352126,RMVar_hsa_circ_199390,RMVar_hsa_circ_361710,RMVar_hsa_circ_344611,RMVar_hsa_circ_305321,RMVar_hsa_circ_57799,RMVar_hsa_circ_38372,RMVar_hsa_circ_90303,RMVar_hsa_circ_199398,RMVar_hsa_circ_199399,RMVar_hsa_circ_125985,RMVar_hsa_circ_360198,RMVar_hsa_circ_370464,RMVar_hsa_circ_285728,RMVar_hsa_circ_110840,RMVar_hsa_circ_199403,RMVar_hsa_circ_54086,RMVar_hsa_circ_199405,RMVar_hsa_circ_199404,RMVar_hsa_circ_199401,RMVar_hsa_circ_199402,RMVar_hsa_circ_30854,RMVar_hsa_circ_365369 53710 RMVar_ID_53710 Human_SNP_ID_834039601 A-to-I Human chr2 - 65107612 65107612 65107612 TTAAAAACCTCCCTACTAAGTCCCAGCTACTCAGGAGGCTGAGGCCTGAGAATCACTTGAACACC TTAAAAACCTCCCTACTAAGTCCCAGCTACTCCGGAGGCTGAGGCCTGAGAATCACTTGAACACC T G RAB1A Ensembl:ENSG00000138069 Protein coding intron GSE100210 HepG2 cell line chr2:65107611..65107612 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_17569694,Human_RBP_ID_22477716 RMVar_hsa_circ_200774 53711 RMVar_ID_53711 Human_SNP_ID_834064598 A-to-I Human chr2 - 135921202 135921202 135921202 GTTTCTGAGCAAGGATGTATTATAGGAATATTAGTGATGTGAAAGATGAGTCGAACTAGAGTCAA GTTTCTGAGCAAGGATGTATTATAGGAATATTTGTGATGTGAAAGATGAGTCGAACTAGAGTCAA T A DARS1 Ensembl:ENSG00000115866 Protein coding intron GSE100210 HepG2 cell line chr2:135921201..135921202 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 2 - RMVar_hsa_circ_7414,RMVar_hsa_circ_82692,RMVar_hsa_circ_203498,RMVar_hsa_circ_37795,RMVar_hsa_circ_203500,RMVar_hsa_circ_79854,RMVar_hsa_circ_203499,RMVar_hsa_circ_25133,RMVar_hsa_circ_83597,RMVar_hsa_circ_203501,RMVar_hsa_circ_266292,RMVar_hsa_circ_203502,RMVar_hsa_circ_267619,RMVar_hsa_circ_18735,RMVar_hsa_circ_51444,RMVar_hsa_circ_328178,RMVar_hsa_circ_29235,RMVar_hsa_circ_53908,RMVar_hsa_circ_203503 53712 RMVar_ID_53712 Human_SNP_ID_834114512 A-to-I Human chr2 + 237552194 237552194 237552194 TTTGCATGACAGCTGAAATGTAAATACTTTTTAAAAAATATGTGATGTGGAAGCTTCTTAAAAGG TTTGCATGACAGCTGAAATGTAAATACTTTTTTAAAAATATGTGATGTGGAAGCTTCTTAAAAGG A T MLPH Ensembl:ENSG00000115648 Protein coding intron GSE47997 K562 cells&HepG2 cells chr2:237552194..237552195 23474544 RNA-Seq:(High) rs73999119 Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 5 pancreas 53713 RMVar_ID_53713 Human_SNP_ID_834137690 A-to-I Human chr2 + 79941678 79941678 79941678 TCTCACTCTGCCACCCAGGCTGAAGTGCAGTGACAAGATCTCGGCTCACTGCAACCTCCACCTCC TCTCACTCTGCCACCCAGGCTGAAGTGCAGTGGCAAGATCTCGGCTCACTGCAACCTCCACCTCC A G CTNNA2 Ensembl:ENSG00000066032 Protein coding intron GSE107867 ASD brains,temporal_cortex chr2:79941677..79941678 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_40505,RMVar_hsa_circ_35302,RMVar_hsa_circ_201455,RMVar_hsa_circ_201454 53714 RMVar_ID_53714 Human_SNP_ID_834151292 A-to-I Human chr2 - 33839969 33839969 33839969 GACTTCCTATCCATTTGACACCATTCGCCACCACATGATGATGCAGTCAGGGTGCAAAGGAACTG GACTTCCTATCCATTTGACACCATTCGCCACCGCATGATGATGCAGTCAGGGTGCAAAGGAACTG T C SLC25A5P2 Ensembl:ENSG00000235064 Pseudogene exon GSE100210 HepG2 cell line chr2:33839968..33839969 29129909 RNA-Seq:(High) rs748537281 Functional Loss SNV ICGC 33..33 33 COCA 3 - Human_miRNA_ID_1842595,Human_miRNA_ID_1905164 53715 RMVar_ID_53715 Human_SNP_ID_834224417 A-to-I Human chr2 + 113640501 113640501 113640501 TAGTTCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGAGATTACCGGCATGCGCCACCACG TAGTTCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGAGATTACCGGCATGCGCCACCACG A G RABL2A Ensembl:ENSG00000144134 Protein coding intron GSE47997 K562 cells&HepG2 cells chr2:113640500..113640501;chr2:113640501..113640502 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 CMDI 1 - RMVar_hsa_circ_5054 53716 RMVar_ID_53716 Human_SNP_ID_834299933 A-to-I Human chr2 + 26112975 26112975 26112975 ATGATGGTGGGCACCTGTAGTCTCAGCTACTCAGGAGGCCAAGGCAGGAGAATCACTTGAACCCA ATGATGGTGGGCACCTGTAGTCTCAGCTACTCGGGAGGCCAAGGCAGGAGAATCACTTGAACCCA A G RAB10 Ensembl:ENSG00000084733 Protein coding intron GSE100210 HepG2 cell line chr2:26112974..26112975 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_57068,RMVar_hsa_circ_324091,RMVar_hsa_circ_197749,RMVar_hsa_circ_92976,RMVar_hsa_circ_197746,RMVar_hsa_circ_87850,RMVar_hsa_circ_197748 53717 RMVar_ID_53717 Human_SNP_ID_834304926 A-to-I Human chr2 - 55576317 55576317 55576317 TTGAGACAGAGTCTCACTCTGTCACCCAGGCTAGAGTGCAGTGGCACAATTTCGGCTCACTGCAA TTGAGACAGAGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGCACAATTTCGGCTCACTGCAA T C PPP4R3B Ensembl:ENSG00000275052 Protein coding intron GSE38233 cultured B-cells chr2:55576316..55576317 24183664 RNA-Seq:(High) rs1241598727 Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_23809,RMVar_hsa_circ_49979,RMVar_hsa_circ_307270,RMVar_hsa_circ_319820,RMVar_hsa_circ_361942,RMVar_hsa_circ_310276,RMVar_hsa_circ_279288,RMVar_hsa_circ_63455,RMVar_hsa_circ_200055,RMVar_hsa_circ_200057,RMVar_hsa_circ_200058,RMVar_hsa_circ_200056,RMVar_hsa_circ_200054,RMVar_hsa_circ_75398,RMVar_hsa_circ_326045,RMVar_hsa_circ_352835,RMVar_hsa_circ_55713,RMVar_hsa_circ_54897,RMVar_hsa_circ_34432,RMVar_hsa_circ_200059,RMVar_hsa_circ_357217,RMVar_hsa_circ_200062,RMVar_hsa_circ_370313,RMVar_hsa_circ_309592,RMVar_hsa_circ_200063,RMVar_hsa_circ_200064,RMVar_hsa_circ_344697,RMVar_hsa_circ_364948,RMVar_hsa_circ_200065,RMVar_hsa_circ_200066 53718 RMVar_ID_53718 Human_SNP_ID_834310886 A-to-I Human chr2 - 58460549 58460549 58460549 TAGTGATGAGGAGGTGGATTATAGCAAAATGGACCAGGGTAACAAGAAGAGAACCTTAAGCCGTT TAGTGATGAGGAGGTGGATTATAGCAAAATGGGCCAGGGTAACAAGAAGAGAACCTTAAGCCGTT T C AC007238.1 Ensembl:ENSG00000231043 Pseudogene exon GSE100210 HepG2 cell line chr2:58460548..58460549 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_1023634 53719 RMVar_ID_53719 Human_SNP_ID_834340431 A-to-I Human chr2 - 53746551 53746551 53746551 TCACTTGAATCCGGGAGGGCGGACATTGCAGTAAGCCAAGATTGCGCCATTGCACTCCAGCTTGG TCACTTGAATCCGGGAGGGCGGACATTGCAGTGAGCCAAGATTGCGCCATTGCACTCCAGCTTGG T C ASB3 Ensembl:ENSG00000115239 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank chr2:53746550..53746551 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_199808,RMVar_hsa_circ_199802,RMVar_hsa_circ_275448,RMVar_hsa_circ_297684,RMVar_hsa_circ_199803,RMVar_hsa_circ_273021,RMVar_hsa_circ_316442,RMVar_hsa_circ_199809,RMVar_hsa_circ_199813,RMVar_hsa_circ_288784,RMVar_hsa_circ_296416,RMVar_hsa_circ_199812,RMVar_hsa_circ_199816,RMVar_hsa_circ_304530,RMVar_hsa_circ_281724,RMVar_hsa_circ_199817,RMVar_hsa_circ_199819,RMVar_hsa_circ_199818,RMVar_hsa_circ_199815,RMVar_hsa_circ_338311,RMVar_hsa_circ_199820 53720 RMVar_ID_53720 Human_SNP_ID_834344937 A-to-I Human chr2 - 176200949 176200949 176200949 AGAAGAAAGTGGAAGCAAAGAAAGAAGAATCCAAGGAGTCTGATGATGACATGGGCCTTGGTCTT AGAAGAAAGTGGAAGCAAAGAAAGAAGAATCCGAGGAGTCTGATGATGACATGGGCCTTGGTCTT T C AC016739.1 Ensembl:ENSG00000218175 Pseudogene exon GSE100210 HepG2 cell line chr2:176200948..176200949 29129909 RNA-Seq:(High) rs879049373 Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_538881,Human_RBP_ID_5100089,Human_RBP_ID_17699967,Human_RBP_ID_18534128 53721 RMVar_ID_53721 Human_SNP_ID_834375855 A-to-I Human chr2 + 138288080 138288080 138288080 TCCTGCAGCACTTCTTTATTCTGCTCTTCACCATCACCCTGCATATCTGAAGTCCATAGTGTCAG TCCTGCAGCACTTCTTTATTCTGCTCTTCACCGTCACCCTGCATATCTGAAGTCCATAGTGTCAG A G - - Other Unknown GSE100210 HepG2 cell line chr2:138288079..138288080 29129909 RNA-Seq:(High) rs878969706 Functional Loss SNV ICGC 33..33 33 LAML 1 - 53722 RMVar_ID_53722 Human_SNP_ID_834406528 A-to-I Human chr2 - 50850037 50850037 50850037 TTTTTCTTTAATTTTTCTTTAATTTTTGTAGAAGTGAGGTCTCACTTTGTTGCCTAGGCTGGTCT TTTTTCTTTAATTTTTCTTTAATTTTTGTAGACGTGAGGTCTCACTTTGTTGCCTAGGCTGGTCT T G NRXN1 Ensembl:ENSG00000179915 Protein coding intron GSE107867 ASD brains,frontal_cortex chr2:50850036..50850037 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 53723 RMVar_ID_53723 Human_SNP_ID_834408775 A-to-I Human chr2 - 31846258 31846248 31846258 ACCCTGTCTCTACCAAAAATACAAAATTAGCCAGGCACGGTGGTGCGCACCTGTAATCCTAGCTA ACCCTGTCTCTACCAAAAATACAAAATTAGCC__________GTGCGCACCTGTAATCCTAGCTA CCACCGTGCCT C - - Other Unknown GSE100210 HepG2 cell line chr2:31846257..31846258 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 33..42 33 LICA 1 - 53724 RMVar_ID_53724 Human_SNP_ID_834451857 A-to-I Human chr2 + 23964011 23964011 23964011 AAAAACTAGCCAGCTTGGTGACACATACCTGTAGACCCAGCTACTGAGGAGGCTGAGACAGGAGG AAAAACTAGCCAGCTTGGTGACACATACCTGTGGACCCAGCTACTGAGGAGGCTGAGACAGGAGG A G UBXN2A Ensembl:ENSG00000173960 Protein coding intron GSE100210 HepG2 cell line chr2:23964010..23964011 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_197544,RMVar_hsa_circ_280098,RMVar_hsa_circ_282244,RMVar_hsa_circ_310286,RMVar_hsa_circ_280474,RMVar_hsa_circ_197545,RMVar_hsa_circ_197542,RMVar_hsa_circ_197543,RMVar_hsa_circ_197541 53725 RMVar_ID_53725 Human_SNP_ID_834455252 A-to-I Human chr2 - 37106955 37106955 37106955 TCACTGCAACTTCTGCCTCTTGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGAT TCACTGCAACTTCTGCCTCTTGGGTTCAAGTGTTTCTCCTGCCTCAGCCTCCTGAGTAGCTGGAT T A EIF2AK2 Ensembl:ENSG00000055332 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells chr2:37106954..37106955 23474544 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 OV,ovary serous_carcinoma 4 ovary 53726 RMVar_ID_53726 Human_SNP_ID_834473667 A-to-I Human chr2 - 216038775 216038775 216038775 ACTGAAAAACAACAAAAACAAAAACACAAATTAGTCGGGTGTGGTGGCACACACCTGTAGTCCCA ACTGAAAAACAACAAAAACAAAAACACAAATTGGTCGGGTGTGGTGGCACACACCTGTAGTCCCA T C PECR Ensembl:ENSG00000115425 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line chr2:216038774..216038775 24183664,29129909,31158229 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_17950210 53727 RMVar_ID_53727 Human_SNP_ID_834531725 A-to-I Human chr2 - 69463784 69463784 69463784 AAAATAGGCTGGGCATGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGCAG AAAATAGGCTGGGCATGGTGGCTCACACCTGTGATCCCAGCACTTTGGGAGGCCAAGGTGGGCAG T C AAK1 Ensembl:ENSG00000115977 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells chr2:69463783..69463784 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - RMVar_hsa_circ_93707,RMVar_hsa_circ_109768,RMVar_hsa_circ_122881,RMVar_hsa_circ_268607,RMVar_hsa_circ_100894,RMVar_hsa_circ_200929,RMVar_hsa_circ_200931,RMVar_hsa_circ_200932,RMVar_hsa_circ_200930 53728 RMVar_ID_53728 Human_SNP_ID_834531728 A-to-I Human chr2 - 69463784 69463784 69463784 AAAATAGGCTGGGCATGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGCAG AAAATAGGCTGGGCATGGTGGCTCACACCTGTCATCCCAGCACTTTGGGAGGCCAAGGTGGGCAG T G AAK1 Ensembl:ENSG00000115977 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells chr2:69463783..69463784 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - RMVar_hsa_circ_93707,RMVar_hsa_circ_109768,RMVar_hsa_circ_122881,RMVar_hsa_circ_268607,RMVar_hsa_circ_100894,RMVar_hsa_circ_200929,RMVar_hsa_circ_200931,RMVar_hsa_circ_200932,RMVar_hsa_circ_200930 53729 RMVar_ID_53729 Human_SNP_ID_834532756 A-to-I Human chr2 - 132195666 132195666 132195666 CTGCCTCAGCTTCTTGAGTAGCTGGGATTACAAGCACCCACCACCGTGCCCTGCTAATTTTTGAA CTGCCTCAGCTTCTTGAGTAGCTGGGATTACATGCACCCACCACCGTGCCCTGCTAATTTTTGAA T A ANKRD30BL Ensembl:ENSG00000163046 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank chr2:132195665..132195666 30559470 RNA-Seq:(High) rs1157115307 Functional Loss SNV ICGC 33..33 33 PBCA 1 - 53730 RMVar_ID_53730 Human_SNP_ID_834685457 A-to-I Human chr2 - 216049363 216049363 216049363 CCTGTTTTATTTTTAAACACAGGGAGTTATTTATTCCCAGACTGCTGTGGAGAACTATGGTTCCT CCTGTTTTATTTTTAAACACAGGGAGTTATTTGTTCCCAGACTGCTGTGGAGAACTATGGTTCCT T C PECR Ensembl:ENSG00000115425 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector chr2:216049362..216049363 29967493 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 COCA 1 - Human_RBP_ID_60885,Human_RBP_ID_19000601 Human_Splice_Rec_356352,Human_Splice_Rec_356366,Human_Splice_Rec_356376,Human_Splice_Rec_356384,Human_Splice_Rec_356396 RMVar_hsa_circ_206797,RMVar_hsa_circ_275754,RMVar_hsa_circ_358707,RMVar_hsa_circ_311057,RMVar_hsa_circ_278163,RMVar_hsa_circ_206799,RMVar_hsa_circ_206798,RMVar_hsa_circ_206801,RMVar_hsa_circ_286145,RMVar_hsa_circ_310741,RMVar_hsa_circ_336960,RMVar_hsa_circ_360955,RMVar_hsa_circ_304950,RMVar_hsa_circ_206802,RMVar_hsa_circ_333092,RMVar_hsa_circ_339792,RMVar_hsa_circ_364278 53731 RMVar_ID_53731 Human_SNP_ID_834687412 A-to-I Human chr2 + 28790139 28790139 28790139 CTCTGTCTCCACAGAAGATACAAAACAGCCAGATGTGGTGGTGTGCACCTGTAGTCCCAGCTTGC CTCTGTCTCCACAGAAGATACAAAACAGCCAGGTGTGGTGGTGTGCACCTGTAGTCCCAGCTTGC A G SPDYA,PPP1CB Ensembl:ENSG00000163806,Ensembl:ENSG00000213639 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells chr2:28790138..28790139 24183664 RNA-Seq:(High) rs7608105 Functional Loss SNV ICGC 33..33 33 ESCA 1 - GWAS_ID_3521,GWAS_ID_3522,GWAS_ID_3523,GWAS_ID_3524,GWAS_ID_3525,GWAS_ID_3526,GWAS_ID_3527,GWAS_ID_3528,GWAS_ID_3529,GWAS_ID_3530,GWAS_ID_3531,GWAS_ID_3532,GWAS_ID_3533,GWAS_ID_3534,GWAS_ID_3535,GWAS_ID_3536,GWAS_ID_3537,GWAS_ID_3538,GWAS_ID_3539,GWAS_ID_3540,GWAS_ID_3541,GWAS_ID_3542,GWAS_ID_3543,GWAS_ID_3544,GWAS_ID_3545,GWAS_ID_3546,GWAS_ID_3547,GWAS_ID_3548,GWAS_ID_3549,GWAS_ID_3550,GWAS_ID_3551,GWAS_ID_3552,GWAS_ID_3553,GWAS_ID_3554,GWAS_ID_3555,GWAS_ID_3556,GWAS_ID_3557 RMVar_hsa_circ_198112,RMVar_hsa_circ_198107,RMVar_hsa_circ_342271,RMVar_hsa_circ_198108,RMVar_hsa_circ_112730,RMVar_hsa_circ_273465,RMVar_hsa_circ_198113,RMVar_hsa_circ_52550,RMVar_hsa_circ_198111,RMVar_hsa_circ_198117,RMVar_hsa_circ_112573,RMVar_hsa_circ_198114,RMVar_hsa_circ_375294,RMVar_hsa_circ_78730,RMVar_hsa_circ_198118,RMVar_hsa_circ_198116 53732 RMVar_ID_53732 Human_SNP_ID_834699289 A-to-I Human chr2 - 111940524 111940524 111940524 CAGGAGCACCTGACACAGGATGCAGTTGCTAAAGCAAATCAAACAAAAGAGGGCTTGCCTGTTGC CAGGAGCACCTGACACAGGATGCAGTTGCTAAGGCAAATCAAACAAAAGAGGGCTTGCCTGTTGC T C RTRAFP1 Ensembl:ENSG00000225496 Pseudogene exon GSE100210 HepG2 cell line chr2:111940523..111940524 29129909 RNA-Seq:(High) rs879061438 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 10 haematopoietic and lymphoid tissue 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 53733 RMVar_ID_53733 Human_SNP_ID_834848507 A-to-I Human chr2 - 61493991 61493991 61493991 CTGGAATCATTTGGCTGCTGAACTCTATAGAGAGAGTCCATTCTCTACATCTGCCTCTCCGTTGC CTGGAATCATTTGGCTGCTGAACTCTATAGAGGGAGTCCATTCTCTACATCTGCCTCTCCGTTGC T C XPO1 Ensembl:ENSG00000082898 Protein coding CDS GSE100210 HepG2 cell line chr2:61493990..61493991 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_553155,Human_RBP_ID_774714,Human_RBP_ID_1588534,Human_RBP_ID_1921062,Human_RBP_ID_2655629,Human_RBP_ID_3630387,Human_RBP_ID_5194626,Human_RBP_ID_8849262,Human_RBP_ID_9296043,Human_RBP_ID_13931505,Human_RBP_ID_18318144,Human_RBP_ID_18763381,Human_RBP_ID_22077083,Human_RBP_ID_23878883,Human_RBP_ID_26338573 Human_Splice_Rec_251479,Human_Splice_Rec_251549,Human_Splice_Rec_251595,Human_Splice_Rec_251643 Human_miRNA_ID_130414,Human_miRNA_ID_131995,Human_miRNA_ID_693130,Human_miRNA_ID_1016792,Human_miRNA_ID_1303082 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 53734 RMVar_ID_53734 Human_SNP_ID_834975081 A-to-I Human chr2 - 33839972 33839972 33839972 GTTGACTTCCTATCCATTTGACACCATTCGCCACCACATGATGATGCAGTCAGGGTGCAAAGGAA GTTGACTTCCTATCCATTTGACACCATTCGCCCCCACATGATGATGCAGTCAGGGTGCAAAGGAA T G SLC25A5P2 Ensembl:ENSG00000235064 Pseudogene exon GSE100210 HepG2 cell line chr2:33839971..33839972 29129909 RNA-Seq:(High) rs770153531 Functional Loss SNV ICGC 33..33 33 COCA 4 - Human_miRNA_ID_1842595,Human_miRNA_ID_1905164 53735 RMVar_ID_53735 Human_SNP_ID_835066447 A-to-I Human chr2 + 138288092 138288092 138288092 TCTTTATTCTGCTCTTCACCATCACCCTGCATATCTGAAGTCCATAGTGTCAGATTATCACGTAA TCTTTATTCTGCTCTTCACCATCACCCTGCATGTCTGAAGTCCATAGTGTCAGATTATCACGTAA A G - - Other Unknown GSE100210 HepG2 cell line chr2:138288091..138288092 29129909 RNA-Seq:(High) rs878981250 Functional Loss SNV ICGC 33..33 33 LAML 2 - 53736 RMVar_ID_53736 Human_SNP_ID_835088127 A-to-I Human chr2 + 170963196 170963116 170963196 GGAGTTCAAGACCAGCCTGGCCAACATGGCAAAACCCCATCTCTACTGAAAAAATATAAACATTA _________________________________ACCCCATCTCTACTGAAAAAATATAAACATTA TAATCCCAGCACTTTGGGAGGCCGAAGTGGGTGGATCACCTGAGGTTAGGAGTTCAAGACCAGCCTGGCCAACATGGCAAA T GORASP2 Ensembl:ENSG00000115806 Protein coding intron GSE38233 cultured B-cells chr2:170963196..170963197 24183664 RNA-Seq:(High) - Functional Loss DEL ICGC 1..33 33 LICA 1 - RMVar_hsa_circ_89579,RMVar_hsa_circ_204578 53737 RMVar_ID_53737 Human_SNP_ID_835089901 A-to-I Human chr2 + 28160157 28160157 28160157 GTATGCACCACCATGCCCAGCTAAGTATTTTTATTTTTGTAGAGTTGGGGCCTCACTAAGTTGCT GTATGCACCACCATGCCCAGCTAAGTATTTTTCTTTTTGTAGAGTTGGGGCCTCACTAAGTTGCT A C BABAM2 Ensembl:ENSG00000158019 Protein coding intron GSE100210 HepG2 cell line chr2:28160156..28160157 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 STAD 1 - RMVar_hsa_circ_17133,RMVar_hsa_circ_83972,RMVar_hsa_circ_198090,RMVar_hsa_circ_15931,RMVar_hsa_circ_350707,RMVar_hsa_circ_49597,RMVar_hsa_circ_56631,RMVar_hsa_circ_67343 53738 RMVar_ID_53738 Human_SNP_ID_835113873 A-to-I Human chr2 - 72669046 72669046 72669046 GTCTTGCTGTGTCACCCAGGCTAGAATGCAATAGTGTGATCAAAACTCACTGTAGACTCAAACGT GTCTTGCTGTGTCACCCAGGCTAGAATGCAATTGTGTGATCAAAACTCACTGTAGACTCAAACGT T A EXOC6B Ensembl:ENSG00000144036 Protein coding intron GSE100210 HepG2 cell line chr2:72669045..72669046 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_127475,RMVar_hsa_circ_201125,RMVar_hsa_circ_21183,RMVar_hsa_circ_40616,RMVar_hsa_circ_28549,RMVar_hsa_circ_16352,RMVar_hsa_circ_370398,RMVar_hsa_circ_43418,RMVar_hsa_circ_62921,RMVar_hsa_circ_201136,RMVar_hsa_circ_71748,RMVar_hsa_circ_48135,RMVar_hsa_circ_41880,RMVar_hsa_circ_117570,RMVar_hsa_circ_356870,RMVar_hsa_circ_201153,RMVar_hsa_circ_327966,RMVar_hsa_circ_81764,RMVar_hsa_circ_201157,RMVar_hsa_circ_315773,RMVar_hsa_circ_80506,RMVar_hsa_circ_201158,RMVar_hsa_circ_340840,RMVar_hsa_circ_289922,RMVar_hsa_circ_28901,RMVar_hsa_circ_310955,RMVar_hsa_circ_315619 53739 RMVar_ID_53739 Human_SNP_ID_835150124 A-to-I Human chr2 - 203485738 203485731 203485738 TGTGACAACTAAAAACGTCCGTAGACATTGTTACATGTTGCTTGTAGGACAAAATCCACCCCCAA TGTGACAACTAAAAACGTCCGTAGACATTGTT_______GCTTGTAGGACAAAATCCACCCCCAA CAACATGT C RAPH1 Ensembl:ENSG00000173166 Protein coding intron GSE100210 HepG2 cell line chr2:203485737..203485738 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 33..39 33 PAAD 1 - RMVar_hsa_circ_359533,RMVar_hsa_circ_356930,RMVar_hsa_circ_206244,RMVar_hsa_circ_374986,RMVar_hsa_circ_45168,RMVar_hsa_circ_32085,RMVar_hsa_circ_206249,RMVar_hsa_circ_206251,RMVar_hsa_circ_104374,RMVar_hsa_circ_341667,RMVar_hsa_circ_343999,RMVar_hsa_circ_206252 53740 RMVar_ID_53740 Human_SNP_ID_835153746 A-to-I Human chr2 - 113740581 113740581 113740581 ATGGATGGGGTGATGGTTGCATAACAGTGTGAATGTACTTTATGCCATTAACTGTACACTTAAAA ATGGATGGGGTGATGGTTGCATAACAGTGTGAGTGTACTTTATGCCATTAACTGTACACTTAAAA T C SLC35F5 Ensembl:ENSG00000115084 Protein coding intron GSE47997 K562 cells&HepG2 cells chr2:113740580..113740581 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 3 oesophagus RMVar_hsa_circ_126620,RMVar_hsa_circ_202695,RMVar_hsa_circ_279872,RMVar_hsa_circ_374988,RMVar_hsa_circ_328181,RMVar_hsa_circ_107917,RMVar_hsa_circ_202696,RMVar_hsa_circ_202698,RMVar_hsa_circ_202697,RMVar_hsa_circ_202705,RMVar_hsa_circ_306170,RMVar_hsa_circ_367316,RMVar_hsa_circ_360414,RMVar_hsa_circ_314184,RMVar_hsa_circ_202706,RMVar_hsa_circ_202704,RMVar_hsa_circ_202708,RMVar_hsa_circ_306896,RMVar_hsa_circ_312794,RMVar_hsa_circ_311575,RMVar_hsa_circ_304085,RMVar_hsa_circ_202709,RMVar_hsa_circ_270193,RMVar_hsa_circ_202707,RMVar_hsa_circ_299389,RMVar_hsa_circ_325230,RMVar_hsa_circ_202714,RMVar_hsa_circ_202715,RMVar_hsa_circ_202713,RMVar_hsa_circ_6763,RMVar_hsa_circ_202719,RMVar_hsa_circ_285887,RMVar_hsa_circ_299327,RMVar_hsa_circ_372867,RMVar_hsa_circ_299168,RMVar_hsa_circ_202720,RMVar_hsa_circ_350812,RMVar_hsa_circ_202717,RMVar_hsa_circ_202718,RMVar_hsa_circ_363539,RMVar_hsa_circ_69707,RMVar_hsa_circ_339481,RMVar_hsa_circ_323696,RMVar_hsa_circ_362734,RMVar_hsa_circ_202722 53741 RMVar_ID_53741 Human_SNP_ID_835197280 A-to-I Human chr2 + 170752506 170752506 170752506 CATCGTCAACCCAAACATCTCCTTGCATTTTTATTGGCTGAATTGGGTACAAGTGGTTCTATAGA CATCGTCAACCCAAACATCTCCTTGCATTTTTGTTGGCTGAATTGGGTACAAGTGGTTCTATAGA A G EIF2S2P4 Ensembl:ENSG00000128692 Pseudogene exon GSE100210 HepG2 cell line chr2:170752505..170752506 29129909 RNA-Seq:(High) rs879177767 Functional Loss SNV ICGC 33..33 33 LICA 2 - 53742 RMVar_ID_53742 Human_SNP_ID_835241727 A-to-I Human chr2 + 110988294 110988294 110988294 ACCTCTGTCTCTACAAAAATAATACAAAAATTAGCCAGGCGTGGTGGCACATGCCTGTGGTCCCA ACCTCTGTCTCTACAAAAATAATACAAAAATTGGCCAGGCGTGGTGGCACATGCCTGTGGTCCCA A G ACOXL Ensembl:ENSG00000153093 Protein coding intron GSE100210 HepG2 cell line chr2:110988293..110988294 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 3 prostate RMVar_hsa_circ_65991,RMVar_hsa_circ_59050,RMVar_hsa_circ_346870,RMVar_hsa_circ_267819 53743 RMVar_ID_53743 Human_SNP_ID_835272563 A-to-I Human chr2 + 202276658 202276658 202276658 GCCCAGGAGTTCAAGACCAGCCTGGGCAATATAGGAAAACCCCATCTCTACCAAAAACAAAAATT GCCCAGGAGTTCAAGACCAGCCTGGGCAATATTGGAAAACCCCATCTCTACCAAAAACAAAAATT A T NOP58 Ensembl:ENSG00000055044 Protein coding intron GSE100210 HepG2 cell line chr2:202276657..202276658 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_14037,RMVar_hsa_circ_93800,RMVar_hsa_circ_115742,RMVar_hsa_circ_43257,RMVar_hsa_circ_205959,RMVar_hsa_circ_84262,RMVar_hsa_circ_205960,RMVar_hsa_circ_205958,RMVar_hsa_circ_375399,RMVar_hsa_circ_22997,RMVar_hsa_circ_205961 53744 RMVar_ID_53744 Human_SNP_ID_835322229 A-to-I Human chr2 - 152141515 152141515 152141515 TTATTTATTTATTTGAGACAGAGTCTTGCTTTATCGCCCAGGCTGGAGTGCAGTGGTGCCATCTC TTATTTATTTATTTGAGACAGAGTCTTGCTTTGTCGCCCAGGCTGGAGTGCAGTGGTGCCATCTC T C STAM2 Ensembl:ENSG00000115145 Protein coding intron GSE100210 HepG2 cell line chr2:152141514..152141515 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - RMVar_hsa_circ_292682,RMVar_hsa_circ_308169,RMVar_hsa_circ_310042,RMVar_hsa_circ_281494,RMVar_hsa_circ_203873,RMVar_hsa_circ_203874,RMVar_hsa_circ_331911,RMVar_hsa_circ_203872,RMVar_hsa_circ_203880,RMVar_hsa_circ_70190,RMVar_hsa_circ_369731,RMVar_hsa_circ_203876,RMVar_hsa_circ_350813,RMVar_hsa_circ_300474,RMVar_hsa_circ_203881,RMVar_hsa_circ_203879,RMVar_hsa_circ_16082 53745 RMVar_ID_53745 Human_SNP_ID_835369147 A-to-I Human chr2 + 202284134 202284134 202284134 TGAAACCCCGTCTCTACTAAAAATACAAAATTAGCTGGGCATGGTGGCTCATGCCTGCAATAATC TGAAACCCCGTCTCTACTAAAAATACAAAATTTGCTGGGCATGGTGGCTCATGCCTGCAATAATC A T NOP58 Ensembl:ENSG00000055044 Protein coding intron GSE38233 cultured B-cells chr2:202284133..202284134 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_14037,RMVar_hsa_circ_115742,RMVar_hsa_circ_43257,RMVar_hsa_circ_205959,RMVar_hsa_circ_84262,RMVar_hsa_circ_205960,RMVar_hsa_circ_51138,RMVar_hsa_circ_63084,RMVar_hsa_circ_331064,RMVar_hsa_circ_324431,RMVar_hsa_circ_125140,RMVar_hsa_circ_308746,RMVar_hsa_circ_334218,RMVar_hsa_circ_335529,RMVar_hsa_circ_277679,RMVar_hsa_circ_69947,RMVar_hsa_circ_205964,RMVar_hsa_circ_205965,RMVar_hsa_circ_205963 53746 RMVar_ID_53746 Human_SNP_ID_835389578 A-to-I Human chr2 + 74418300 74418300 74418300 CCCGAGGTCTCTTAGGTGTTGGCACTTCGCTGAGCTCCTTCTGACTCCCTACCAGCGCTGTCCTG CCCGAGGTCTCTTAGGTGTTGGCACTTCGCTGGGCTCCTTCTGACTCCCTACCAGCGCTGTCCTG A G - - Other Unknown GSE100210 HepG2 cell line chr2:74418299..74418300 29129909 RNA-Seq:(High) rs956708866 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue 53747 RMVar_ID_53747 Human_SNP_ID_835398050 A-to-I Human chr2 - 127290960 127290960 127290960 CTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTATAGGCGCCCGTCACCATGCCCGGCTAATTTTT CTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTGTAGGCGCCCGTCACCATGCCCGGCTAATTTTT T C ERCC3 Ensembl:ENSG00000163161 Protein coding intron GSE100210 HepG2 cell line chr2:127290959..127290960 29129909 RNA-Seq:(High) rs1396675660 Functional Loss SNV ICGC 33..33 33 PRAD 1 - 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_94418,RMVar_hsa_circ_301574,RMVar_hsa_circ_203069 53748 RMVar_ID_53748 Human_SNP_ID_835443503 A-to-I Human chr2 - 218652365 218652365 218652365 ATTAAAAGATTCACCTACATTTTCTACTAGTAACTAACTCCTATGAGTCTTGTTCCATCTGATTC ATTAAAAGATTCACCTACATTTTCTACTAGTAGCTAACTCCTATGAGTCTTGTTCCATCTGATTC T C ZNF142 Ensembl:ENSG00000115568 Protein coding intron GSE38233 cultured B-cells chr2:218652364..218652365 24183664 RNA-Seq:(High) rs4674323 Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus squamous_cell_carcinoma,ESCA 3 oesophagus RMVar_hsa_circ_108325,RMVar_hsa_circ_87582,RMVar_hsa_circ_206999,RMVar_hsa_circ_116211,RMVar_hsa_circ_207001,RMVar_hsa_circ_207003,RMVar_hsa_circ_207005,RMVar_hsa_circ_374083,RMVar_hsa_circ_26259 53749 RMVar_ID_53749 Human_SNP_ID_835453762 A-to-I Human chr2 + 241319617 241319617 241319617 AAGCAGTTTTCCTTTTTTTCTTTTTTTGAGACAGTCTCACTCTGTCACCCAGGCTGGAGTGCAGC AAGCAGTTTTCCTTTTTTTCTTTTTTTGAGACCGTCTCACTCTGTCACCCAGGCTGGAGTGCAGC A C SEPTIN2 Ensembl:ENSG00000168385 Protein coding intron GSE100210 HepG2 cell line chr2:241319616..241319617 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 oesophagus adenocarcinoma 7 oesophagus Human_RBP_ID_13823096 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_29898 53750 RMVar_ID_53750 Human_SNP_ID_835466500 A-to-I Human chr2 + 86140817 86140817 86140817 AAATGCTGTCCAGGCCAGGCACAGTGGCTCACACCTGTAATCCCAGGACTTCGGGAGGCTGAGGC AAATGCTGTCCAGGCCAGGCACAGTGGCTCACGCCTGTAATCCCAGGACTTCGGGAGGCTGAGGC A G PTCD3 Ensembl:ENSG00000132300 Protein coding 3'UTR GSE107867 ASD brains,cerebellum chr2:86140816..86140817 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ORCA 1 - RMVar_hsa_circ_121328,RMVar_hsa_circ_201646,RMVar_hsa_circ_85803,RMVar_hsa_circ_201669 53751 RMVar_ID_53751 Human_SNP_ID_835488261 A-to-I Human chr2 - 111940549 111940549 111940549 GCTTAAGGCAATTCAAATTTTGGTTCAGGAGCACCTGACACAGGATGCAGTTGCTAAAGCAAATC GCTTAAGGCAATTCAAATTTTGGTTCAGGAGCGCCTGACACAGGATGCAGTTGCTAAAGCAAATC T C RTRAFP1 Ensembl:ENSG00000225496 Pseudogene exon GSE100210 HepG2 cell line chr2:111940548..111940549 29129909 RNA-Seq:(High) rs879034985 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 10 haematopoietic and lymphoid tissue Human_miRNA_ID_1842600,Human_miRNA_ID_1905169,Human_miRNA_ID_2234008,Human_miRNA_ID_2234009,Human_miRNA_ID_2234010,Human_miRNA_ID_3028164,Human_miRNA_ID_3028165,Human_miRNA_ID_3028166 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 53752 RMVar_ID_53752 Human_SNP_ID_835499824 A-to-I Human chr2 + 202280606 202280606 202280606 CACCCGCCTTGGCCTCCCAAAGTGCTGGGATTACAAGCATGAGCCACCGTGCCTGGCCATCATTT CACCCGCCTTGGCCTCCCAAAGTGCTGGGATTGCAAGCATGAGCCACCGTGCCTGGCCATCATTT A G NOP58 Ensembl:ENSG00000055044 Protein coding intron GSE38233 cultured B-cells chr2:202280605..202280606 24183664 RNA-Seq:(High) rs1559261852 Functional Loss SNV ICGC 33..33 33 MALY 1 - RMVar_hsa_circ_14037,RMVar_hsa_circ_115742,RMVar_hsa_circ_43257,RMVar_hsa_circ_205959,RMVar_hsa_circ_84262,RMVar_hsa_circ_205960,RMVar_hsa_circ_19358,RMVar_hsa_circ_63084,RMVar_hsa_circ_331064,RMVar_hsa_circ_324431,RMVar_hsa_circ_291473,RMVar_hsa_circ_205962 53753 RMVar_ID_53753 Human_SNP_ID_835584923 A-to-I Human chr2 - 91655377 91655377 91655377 GAAGTACAGGCTCAGTCTGCGGCCAAGACTCCATCCTGCAAGGTAAGGTCCCCTCCAGGGGCAAG GAAGTACAGGCTCAGTCTGCGGCCAAGACTCCGTCCTGCAAGGTAAGGTCCCCTCCAGGGGCAAG T C LSP1P4 Ensembl:ENSG00000143429 Pseudogene exon GSE100210 HepG2 cell line chr2:91655376..91655377 29129909 RNA-Seq:(High) rs112527890 Functional Loss SNV ICGC 33..33 33 RT 1 - Human_RBP_ID_918402,Human_RBP_ID_9384210,Human_RBP_ID_18999851 Human_Splice_Rec_272953,Human_Splice_Rec_272957,Human_Splice_Rec_272959,Human_Splice_Rec_272963,Human_Splice_Rec_272969,Human_Splice_Rec_272973 53754 RMVar_ID_53754 Human_SNP_ID_835683035 A-to-I Human chr2 - 50599044 50599044 50599044 GAGTTGGCCAGACATGGTGGCTCACACCTGTAATCCTAGCACTTTGGGAGGCTGAGGCGAGTGGA GAGTTGGCCAGACATGGTGGCTCACACCTGTACTCCTAGCACTTTGGGAGGCTGAGGCGAGTGGA T G NRXN1 Ensembl:ENSG00000179915 Protein coding intron GSE107867 ASD brains,cerebellum chr2:50599043..50599044 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 9 pancreas RMVar_hsa_circ_6943,RMVar_hsa_circ_36864,RMVar_hsa_circ_294728,RMVar_hsa_circ_307129,RMVar_hsa_circ_268420,RMVar_hsa_circ_292093,RMVar_hsa_circ_327433,RMVar_hsa_circ_268933,RMVar_hsa_circ_329013,RMVar_hsa_circ_279431,RMVar_hsa_circ_295343,RMVar_hsa_circ_308859,RMVar_hsa_circ_312149,RMVar_hsa_circ_326022,RMVar_hsa_circ_7426,RMVar_hsa_circ_35984,RMVar_hsa_circ_377042,RMVar_hsa_circ_265207,RMVar_hsa_circ_279154,RMVar_hsa_circ_199764,RMVar_hsa_circ_199765,RMVar_hsa_circ_320755,RMVar_hsa_circ_346070 53755 RMVar_ID_53755 Human_SNP_ID_835683626 A-to-I Human chr2 + 231434016 231434016 231434016 TATGTTATTGCCTTGACTTCTGTTCCCTGAGGATGCTTGGACAATGAAAACTCTTCTCCCCACCC TATGTTATTGCCTTGACTTCTGTTCCCTGAGGGTGCTTGGACAATGAAAACTCTTCTCCCCACCC A G - - Other Unknown GSE100210 HepG2 cell line chr2:231434015..231434016 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 1 - 53756 RMVar_ID_53756 Human_SNP_ID_835706164 A-to-I Human chr2 - 96982427 96982427 96982427 GAAACTCCATCTCTACAAAAAATACAAAAATTAACCAGGCATGGTGGTGCACGCCTGTCGTCCCA GAAACTCCATCTCTACAAAAAATACAAAAATTGACCAGGCATGGTGGTGCACGCCTGTCGTCCCA T C FAM178B Ensembl:ENSG00000168754 Protein coding intron GSE100210 HepG2 cell line chr2:96982426..96982427 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_103671,RMVar_hsa_circ_201922 53757 RMVar_ID_53757 Human_SNP_ID_835736214 A-to-I Human chr2 - 219075555 219075555 219075555 GTGTGTGGAGACAAGGCTTTGCCATGTTGCCCAGGCTGGTCTTGAACTCCTGGACTCTAGTGATC GTGTGTGGAGACAAGGCTTTGCCATGTTGCCCCGGCTGGTCTTGAACTCCTGGACTCTAGTGATC T G AC068946.1,NHEJ1 Ensembl:ENSG00000280537,Ensembl:ENSG00000187736 Protein coding,Protein coding exon,3'UTR GSE100210 HepG2 cell line chr2:219075554..219075555 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 2 prostate Human_RBP_ID_544541 53758 RMVar_ID_53758 Human_SNP_ID_835745957 A-to-I Human chr2 - 176201133 176201133 176201133 GCCCTCATTAAAGCAGCCGGTGTAAATGTTGAACCTTTTTGGCCTGGCTTGTTTGCAAAGGCCCT GCCCTCATTAAAGCAGCCGGTGTAAATGTTGAGCCTTTTTGGCCTGGCTTGTTTGCAAAGGCCCT T C AC016739.1 Ensembl:ENSG00000218175 Pseudogene exon GSE100210 HepG2 cell line chr2:176201132..176201133 29129909 RNA-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 53759 RMVar_ID_53759 Human_SNP_ID_835788461 A-to-I Human chr2 + 231434057 231434057 231434057 CAATGAAAACTCTTCTCCCCACCCAATTGATCATAATTTGAAATTTCTTTGATCAATACTAAGTA CAATGAAAACTCTTCTCCCCACCCAATTGATCGTAATTTGAAATTTCTTTGATCAATACTAAGTA A G - - Other Unknown GSE100210 HepG2 cell line chr2:231434056..231434057 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 1 - 53760 RMVar_ID_53760 Human_SNP_ID_835809295 A-to-I Human chr2 - 113595713 113595713 113595713 TCCTCGGGCTCCGGCTTGGTGCTCACGCACACAGGAAAGTCCTTCAGCTTCTCCTGGGAGGGCCA TCCTCGGGCTCCGGCTTGGTGCTCACGCACACGGGAAAGTCCTTCAGCTTCTCCTGGGAGGGCCA T C lnc-SLC35F5-17 RNACentral:URS00008BF43D lincRNA intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr2:113595712..113595713 30559470 RNA-Seq:(High) rs773670713 Functional Loss SNV ICGC 33..33 33 LICA 7 - 53761 RMVar_ID_53761 Human_SNP_ID_835819086 A-to-I Human chr2 - 28853610 28853610 28853610 GCTACTCTCAAACTCCTGACCTCAGGTGATCCACCCGCCTGGGCTCCCAAAGTGCTGGGATTATA GCTACTCTCAAACTCCTGACCTCAGGTGATCCCCCCGCCTGGGCTCCCAAAGTGCTGGGATTATA T G TRMT61B Ensembl:ENSG00000171103 Protein coding intron GSE100210 HepG2 cell line chr2:28853609..28853610 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - RMVar_hsa_circ_282561,RMVar_hsa_circ_271089,RMVar_hsa_circ_198127,RMVar_hsa_circ_198128,RMVar_hsa_circ_366187 53762 RMVar_ID_53762 Human_SNP_ID_835957143 A-to-I Human chr2 - 27346969 27346969 27346969 TTTCTTGGCCAGACATGGTGGCTTACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGAGG TTTCTTGGCCAGACATGGTGGCTTACACCTGTGATCCCAGCACTTTGGGAGGCCAAGGTGGGAGG T C GTF3C2 Ensembl:ENSG00000115207 Protein coding intron GSE38233 cultured B-cells chr2:27346968..27346969 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_103493,RMVar_hsa_circ_197976,RMVar_hsa_circ_25458,RMVar_hsa_circ_197986,RMVar_hsa_circ_128167,RMVar_hsa_circ_364979,RMVar_hsa_circ_368158 53763 RMVar_ID_53763 Human_SNP_ID_835995693 A-to-I Human chr2 - 27066131 27066131 27066131 CTCCTGCATCCCAAGTAGCTGGGACAACAGGCACACGCCACCAAGCCCAGCTAATTTTTAAATTT CTCCTGCATCCCAAGTAGCTGGGACAACAGGCTCACGCCACCAAGCCCAGCTAATTTTTAAATTT T A - - Other Unknown GSE100210 HepG2 cell line chr2:27066130..27066131 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - 53764 RMVar_ID_53764 Human_SNP_ID_836021917 A-to-I Human chr2 + 159003900 159003900 159003900 ACTTCAGGCTCAGGTCCAGATAGGGGGCAAGGATACAGCTCGCAGAAAGAAGAAGGTGGTACATA ACTTCAGGCTCAGGTCCAGATAGGGGGCAAGGGTACAGCTCGCAGAAAGAAGAAGGTGGTACATA A G TANC1 Ensembl:ENSG00000115183 Protein coding intron GSE47997 K562 cells&HepG2 cells chr2:159003899..159003900 23474544 RNA-Seq:(High) rs1486900170 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue Human_miRNA_ID_2489628,Human_miRNA_ID_2751706 RMVar_hsa_circ_204014,RMVar_hsa_circ_306123,RMVar_hsa_circ_354222,RMVar_hsa_circ_358287,RMVar_hsa_circ_353754,RMVar_hsa_circ_67915,RMVar_hsa_circ_122905,RMVar_hsa_circ_204016,RMVar_hsa_circ_204015 53765 RMVar_ID_53765 Human_SNP_ID_836054841 A-to-I Human chr2 + 207754755 207754755 207754755 AACTTCCTGGTCTCAAGCCATCCTCTAGCCTCAGCCACACAAGTAGCTGGGACTACAAGTGCAAC AACTTCCTGGTCTCAAGCCATCCTCTAGCCTCGGCCACACAAGTAGCTGGGACTACAAGTGCAAC A G CCNYL1 Ensembl:ENSG00000163249 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line chr2:207754754..207754755 23474544,24183664,29129909,31158229,31158229,31158229 RNA-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 53766 RMVar_ID_53766 Human_SNP_ID_836070567 A-to-I Human chr2 + 32177436 32177436 32177436 CCTCAGCCTCCCAAGTAGCTGGGATTACAGGCATGTACCACCAGGCACGGCTAATTTTTTGTATT CCTCAGCCTCCCAAGTAGCTGGGATTACAGGCGTGTACCACCAGGCACGGCTAATTTTTTGTATT A G SLC30A6 Ensembl:ENSG00000152683 Protein coding intron GSE38233 cultured B-cells chr2:32177435..32177436 24183664 RNA-Seq:(High) rs750104477 Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_283701,RMVar_hsa_circ_341621,RMVar_hsa_circ_6276,RMVar_hsa_circ_15613,RMVar_hsa_circ_38520,RMVar_hsa_circ_198297,RMVar_hsa_circ_267835,RMVar_hsa_circ_289412,RMVar_hsa_circ_318725,RMVar_hsa_circ_370122,RMVar_hsa_circ_268828,RMVar_hsa_circ_16231,RMVar_hsa_circ_198299,RMVar_hsa_circ_198301,RMVar_hsa_circ_198302,RMVar_hsa_circ_198300,RMVar_hsa_circ_20267,RMVar_hsa_circ_198298 53767 RMVar_ID_53767 Human_SNP_ID_836074006 A-to-I Human chr2 - 37144819 37144819 37144819 CCAGCACTTTGGTAGGTCAAGGTAGGTGGATCACTTGAATTTGGGAGTTTGAGATTAGCCTAGGC CCAGCACTTTGGTAGGTCAAGGTAGGTGGATCTCTTGAATTTGGGAGTTTGAGATTAGCCTAGGC T A EIF2AK2 Ensembl:ENSG00000055332 Protein coding intron GSE38233 cultured B-cells chr2:37144818..37144819 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_48602,RMVar_hsa_circ_13772,RMVar_hsa_circ_341163,RMVar_hsa_circ_32277,RMVar_hsa_circ_122724,RMVar_hsa_circ_93727,RMVar_hsa_circ_198955,RMVar_hsa_circ_49371,RMVar_hsa_circ_198956,RMVar_hsa_circ_365805 53768 RMVar_ID_53768 Human_SNP_ID_836100568 A-to-I Human chr2 + 207754807 207754807 207754807 CTACAAGTGCAACTGGCACCTGTCTCCTGAATATTAAGCTTTTAATTTTTTGTTTCGGTCACTCT CTACAAGTGCAACTGGCACCTGTCTCCTGAATGTTAAGCTTTTAATTTTTTGTTTCGGTCACTCT A G MIR4775,CCNYL1 Ensembl:ENSG00000284079,Ensembl:ENSG00000163249 miRNA,Protein coding exon,3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr2:207754806..207754807 24183664,29129909 RNA-Seq:(High) rs1187453694 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue Human_miRNA_ID_2764834 RMVar_hsa_circ_206420,RMVar_hsa_circ_99464 53769 RMVar_ID_53769 Human_SNP_ID_836120277 A-to-I Human chr2 - 141743686 141743686 141743686 CATGAGAAACTCCAAAACCAGAACATTTTATTACGGCTTTAGTGTTGTTGCTTGCTATTGAACAG CATGAGAAACTCCAAAACCAGAACATTTTATTTCGGCTTTAGTGTTGTTGCTTGCTATTGAACAG T A LRP1B Ensembl:ENSG00000168702 Protein coding intron GSE100210 HepG2 cell line chr2:141743685..141743686 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - RMVar_hsa_circ_121478,RMVar_hsa_circ_203553,RMVar_hsa_circ_118491,RMVar_hsa_circ_203571,RMVar_hsa_circ_82511,RMVar_hsa_circ_203606,RMVar_hsa_circ_18654,RMVar_hsa_circ_77134,RMVar_hsa_circ_203611,RMVar_hsa_circ_203616,RMVar_hsa_circ_81775,RMVar_hsa_circ_377585,RMVar_hsa_circ_203629 53770 RMVar_ID_53770 Human_SNP_ID_836122792 A-to-I Human chr2 - 84431611 84431610 84431612 TTTTAATGGAACAGATTTTATTGACTGCCTCGAAATCTTTTTGAACGATTCTGCCACAGAAGGCA TTTTAATGGAACAGATTTTATTGACTGCCTC__AATCTTTTTGAACGATTCTGCCACAGAAGGCA TTC T SUCLG1 Ensembl:ENSG00000163541 Protein coding CDS GSE100210 HepG2 cell line chr2:84431610..84431611 29129909 RNA-Seq:(High) - Functional Loss DEL TCGA 32..33 33 SKCM 1 - Human_RBP_ID_556382,Human_RBP_ID_1024351,Human_RBP_ID_1923900,Human_RBP_ID_2666515,Human_RBP_ID_9347559,Human_RBP_ID_13969639,Human_RBP_ID_17964695,Human_RBP_ID_22667457,Human_RBP_ID_23886810 Human_Splice_Rec_267512,Human_Splice_Rec_267532,Human_Splice_Rec_267538,Human_Splice_Rec_267544 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_37765,RMVar_hsa_circ_201484,RMVar_hsa_circ_281322,RMVar_hsa_circ_201485 53771 RMVar_ID_53771 Human_SNP_ID_836123852 A-to-I Human chr2 - 65179142 65179142 65179142 GCCTTGGACTTCTATGCTCAAGCAATCCTCCCACCTCAGCTTCCCAAGTAGCTGGGACTATAGGC GCCTTGGACTTCTATGCTCAAGCAATCCTCCCGCCTCAGCTTCCCAAGTAGCTGGGACTATAGGC T C lnc-RAB1A-11 RNACentral:URS0000D58CC3 lincRNA intron GSE100210 HepG2 cell line chr2:65179141..65179142 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - 53772 RMVar_ID_53772 Human_SNP_ID_836155125 A-to-I Human chr2 - 69323840 69323840 69323840 GAAACCCCGTCTTTACTAAAAATACAAAAATTAGCTGGGAGTGGTGGCGTGCGCCTGTAGTCCCA GAAACCCCGTCTTTACTAAAAATACAAAAATTGGCTGGGAGTGGTGGCGTGCGCCTGTAGTCCCA T C GFPT1 Ensembl:ENSG00000198380 Protein coding 3'UTR GSE100210 HepG2 cell line chr2:69323839..69323840 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 3 breast RMVar_hsa_circ_266238 53773 RMVar_ID_53773 Human_SNP_ID_836170747 A-to-I Human chr2 - 55674182 55674182 55674182 TTAGCTATTTCTAATGCAATAGAAAAAATTCTATTATTCAGTCCTTTAGTTGGCTTACTTGAAAC TTAGCTATTTCTAATGCAATAGAAAAAATTCTGTTATTCAGTCCTTTAGTTGGCTTACTTGAAAC T C PNPT1 Ensembl:ENSG00000138035 Protein coding intron GSE38233 cultured B-cells chr2:55674181..55674182 24183664 RNA-Seq:(High) rs12617829 Functional Loss SNV ICGC 33..33 33 LAML 1 - GWAS_ID_6604,GWAS_ID_6605,GWAS_ID_6606,GWAS_ID_6607,GWAS_ID_6608,GWAS_ID_6609 RMVar_hsa_circ_1092,RMVar_hsa_circ_95213,RMVar_hsa_circ_113405,RMVar_hsa_circ_120288,RMVar_hsa_circ_200079,RMVar_hsa_circ_200080,RMVar_hsa_circ_200083,RMVar_hsa_circ_367895,RMVar_hsa_circ_119178,RMVar_hsa_circ_200089,RMVar_hsa_circ_109983,RMVar_hsa_circ_31717,RMVar_hsa_circ_200092,RMVar_hsa_circ_200093,RMVar_hsa_circ_57208,RMVar_hsa_circ_91094,RMVar_hsa_circ_200094,RMVar_hsa_circ_357916,RMVar_hsa_circ_200104,RMVar_hsa_circ_64638,RMVar_hsa_circ_200099,RMVar_hsa_circ_266803,RMVar_hsa_circ_124374,RMVar_hsa_circ_200102,RMVar_hsa_circ_99184,RMVar_hsa_circ_324216,RMVar_hsa_circ_329333,RMVar_hsa_circ_29288,RMVar_hsa_circ_377349,RMVar_hsa_circ_341692,RMVar_hsa_circ_64870,RMVar_hsa_circ_14021,RMVar_hsa_circ_9112,RMVar_hsa_circ_50100,RMVar_hsa_circ_47920,RMVar_hsa_circ_364807,RMVar_hsa_circ_314778,RMVar_hsa_circ_300426,RMVar_hsa_circ_200106,RMVar_hsa_circ_200107,RMVar_hsa_circ_334922,RMVar_hsa_circ_314053,RMVar_hsa_circ_325657,RMVar_hsa_circ_343703,RMVar_hsa_circ_200110,RMVar_hsa_circ_71823 53774 RMVar_ID_53774 Human_SNP_ID_836179446 A-to-I Human chr2 - 10662978 10662978 10662978 ACAGAGTTGGCCTGTTAGACTGCGCCTTAAACAGTGTCACAGCAGATTCAGAGTAAGTAGAAATT ACAGAGTTGGCCTGTTAGACTGCGCCTTAAACGGTGTCACAGCAGATTCAGAGTAAGTAGAAATT T C NOL10 Ensembl:ENSG00000115761 Protein coding CDS GSE100210 HepG2 cell line chr2:10662977..10662978 29129909 RNA-Seq:(High) rs201462244 Functional Loss SNV ICGC,COSMIC 33..33 33 stomach adenocarcinoma,COCA 4 stomach Human_RBP_ID_1895025,Human_RBP_ID_3957601,Human_RBP_ID_13570290,Human_RBP_ID_18998930,Human_RBP_ID_19099281 Human_Splice_Rec_217672,Human_Splice_Rec_217673,Human_Splice_Rec_217712,Human_Splice_Rec_217713,Human_Splice_Rec_217748,Human_Splice_Rec_217749,Human_Splice_Rec_217778,Human_Splice_Rec_217779 RMVar_hsa_circ_47263,RMVar_hsa_circ_196964,RMVar_hsa_circ_348261,RMVar_hsa_circ_61610,RMVar_hsa_circ_67183,RMVar_hsa_circ_51498,RMVar_hsa_circ_1773,RMVar_hsa_circ_196968,RMVar_hsa_circ_362737,RMVar_hsa_circ_94451,RMVar_hsa_circ_117870,RMVar_hsa_circ_196973,RMVar_hsa_circ_196977,RMVar_hsa_circ_196976,RMVar_hsa_circ_336499,RMVar_hsa_circ_286973,RMVar_hsa_circ_272543,RMVar_hsa_circ_31475,RMVar_hsa_circ_196982,RMVar_hsa_circ_196984,RMVar_hsa_circ_196983,RMVar_hsa_circ_333690,RMVar_hsa_circ_196981,RMVar_hsa_circ_293414,RMVar_hsa_circ_51472,RMVar_hsa_circ_196987,RMVar_hsa_circ_196988,RMVar_hsa_circ_196989,RMVar_hsa_circ_311380,RMVar_hsa_circ_295924,RMVar_hsa_circ_114714,RMVar_hsa_circ_310521,RMVar_hsa_circ_196990,RMVar_hsa_circ_301232,RMVar_hsa_circ_58317,RMVar_hsa_circ_196991,RMVar_hsa_circ_196992 53775 RMVar_ID_53775 Human_SNP_ID_836207699 A-to-I Human chr2 - 71119958 71119958 71119958 ACCTGGAACTCCTGAGCTCAAGCGACCCTCCTACCTCAGCCTCCTGAGTAGCTACGGCTACAGGC ACCTGGAACTCCTGAGCTCAAGCGACCCTCCTGCCTCAGCCTCCTGAGTAGCTACGGCTACAGGC T C MCEE Ensembl:ENSG00000124370 Protein coding intron GSE100210 HepG2 cell line chr2:71119957..71119958 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 53776 RMVar_ID_53776 Human_SNP_ID_836213156 A-to-I Human chr2 - 48128916 48128916 48128916 GCTTGGGAGGCTGAGGCACAGGAATTGCTTGAACCCAGGAGGTGGAGGTTGCAGTGAGCCGAGTT GCTTGGGAGGCTGAGGCACAGGAATTGCTTGAGCCCAGGAGGTGGAGGTTGCAGTGAGCCGAGTT T C AC092650.1 Ensembl:ENSG00000230773 lincRNA intron GSE100210 HepG2 cell line chr2:48128915..48128916 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 53777 RMVar_ID_53777 Human_SNP_ID_836230589 A-to-I Human chr2 - 170997825 170997825 170997825 TAGTAACCTTTTTTCTCTCCCACAAAACTTACAGGTATTTACCTCCTGAGTGTTTTGTAGTTGGA TAGTAACCTTTTTTCTCTCCCACAAAACTTACGGGTATTTACCTCCTGAGTGTTTTGTAGTTGGA T C TLK1 Ensembl:ENSG00000198586 Protein coding intron GSE38233 cultured B-cells chr2:170997824..170997825 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 5 liver Human_RBP_ID_22667931 RMVar_hsa_circ_111553,RMVar_hsa_circ_127504,RMVar_hsa_circ_367800,RMVar_hsa_circ_204579,RMVar_hsa_circ_204580 53778 RMVar_ID_53778 Human_SNP_ID_836237694 A-to-I Human chr2 - 216610933 216610933 216610933 ACAATCATGTCTATTATGTCCTATAACGGAGGAGCCATCATGGCCATGAAGGGGAAGAACCGTGT ACAATCATGTCTATTATGTCCTATAACGGAGGGGCCATCATGGCCATGAAGGGGAAGAACCGTGT T C PSMB3P2 Ensembl:ENSG00000235444 Pseudogene exon GSE100210 HepG2 cell line chr2:216610932..216610933 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_miRNA_ID_1839059,Human_miRNA_ID_1855166 53779 RMVar_ID_53779 Human_SNP_ID_836246627 A-to-I Human chr2 - 127292055 127292055 127292055 TCATGTGAGTACACAATGGGAAGGTGGTCCATAGACAAGAGCCTTCACCAGAAACTGAATCGGCT TCATGTGAGTACACAATGGGAAGGTGGTCCATGGACAAGAGCCTTCACCAGAAACTGAATCGGCT T C ERCC3 Ensembl:ENSG00000163161 Protein coding intron GSE38233 cultured B-cells chr2:127292054..127292055 24183664 RNA-Seq:(High) rs4150407 Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 2 liver GWAS_ID_1611,GWAS_ID_1612,GWAS_ID_1613,GWAS_ID_1614,GWAS_ID_1615,GWAS_ID_1616,GWAS_ID_1617,GWAS_ID_1618,GWAS_ID_1619,GWAS_ID_1620,GWAS_ID_1621,GWAS_ID_1622,GWAS_ID_1623,GWAS_ID_1624,GWAS_ID_1625,GWAS_ID_1626,GWAS_ID_1627 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_94418,RMVar_hsa_circ_301574,RMVar_hsa_circ_203069 53780 RMVar_ID_53780 Human_SNP_ID_836247137 A-to-I Human chr2 - 201009847 201009820 201009848 TGCCCACCTTGGCCTCCCGAAGTGCTGGGATTACAGGCGTGAGCCACCGCGCCTGGCCTGGATGG TGCCCACCTTGGCCTCCCGAAGTGCTGGGAT____________________________GGATGG CAGGCCAGGCGCGGTGGCTCACGCCTGTA C FAM126B Ensembl:ENSG00000155744 Protein coding intron GSE38233 cultured B-cells chr2:201009846..201009847 24183664 RNA-Seq:(High) - Functional Loss DEL ICGC 32..59 33 PRAD 1 - RMVar_hsa_circ_205863,RMVar_hsa_circ_22681,RMVar_hsa_circ_266309,RMVar_hsa_circ_342207,RMVar_hsa_circ_324559,RMVar_hsa_circ_10126,RMVar_hsa_circ_50991,RMVar_hsa_circ_289864,RMVar_hsa_circ_336646,RMVar_hsa_circ_71860,RMVar_hsa_circ_205859,RMVar_hsa_circ_205860,RMVar_hsa_circ_339190,RMVar_hsa_circ_61759,RMVar_hsa_circ_363773,RMVar_hsa_circ_284295,RMVar_hsa_circ_294531,RMVar_hsa_circ_313376,RMVar_hsa_circ_205861,RMVar_hsa_circ_328625,RMVar_hsa_circ_297510,RMVar_hsa_circ_46301,RMVar_hsa_circ_283908,RMVar_hsa_circ_205865,RMVar_hsa_circ_205866,RMVar_hsa_circ_205864,RMVar_hsa_circ_205862 53781 RMVar_ID_53781 Human_SNP_ID_836348837 A-to-I Human chr2 - 37817177 37817177 37817177 ATTTATGAGCCAAGGTCATCAATTCATCTCCTAAGACAGCATCCCACACTTTGGCTGTGAAATCT ATTTATGAGCCAAGGTCATCAATTCATCTCCTGAGACAGCATCCCACACTTTGGCTGTGAAATCT T C - - Other Unknown GSE100210 HepG2 cell line chr2:37817176..37817177 29129909 RNA-Seq:(High) rs1370674772 Functional Loss SNV ICGC 33..33 33 LAML 1 - 53782 RMVar_ID_53782 Human_SNP_ID_836351453 A-to-I Human chr2 - 85326828 85326827 85326828 CTCATGCTTTCAAAACCGAATCTGGGGAGGAAACTGACCTCATTTCTCCCCCGCAGGAGGAAGTT CTCATGCTTTCAAAACCGAATCTGGGGAGGAA_CTGACCTCATTTCTCCCCCGCAGGAGGAAGTT GT G TGOLN2 Ensembl:ENSG00000152291 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector chr2:85326827..85326828 29967493 RNA-Seq:(High) - Functional Loss DEL TCGA 33..33 33 KIRP 1 - Human_RBP_ID_17962425,Human_RBP_ID_18766412,Human_RBP_ID_22669156,Human_RBP_ID_22765870,Human_RBP_ID_27482103 RMVar_hsa_circ_53992 53783 RMVar_ID_53783 Human_SNP_ID_836470609 A-to-I Human chr2 - 141693951 141693951 141693951 TTCCTAGTCCACTTTGTTTGTGTTTTTAGGCAACCTAGACAAACTTCTCAATTCATGTGGCTTCT TTCCTAGTCCACTTTGTTTGTGTTTTTAGGCAGCCTAGACAAACTTCTCAATTCATGTGGCTTCT T C LRP1B Ensembl:ENSG00000168702 Protein coding intron GSE107867 ASD brains,frontal_cortex;ASD brains,temporal_cortex chr2:141693950..141693951 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_121478,RMVar_hsa_circ_203553,RMVar_hsa_circ_118491,RMVar_hsa_circ_203571,RMVar_hsa_circ_82511,RMVar_hsa_circ_203606,RMVar_hsa_circ_18654,RMVar_hsa_circ_77134,RMVar_hsa_circ_203611,RMVar_hsa_circ_203616,RMVar_hsa_circ_81775,RMVar_hsa_circ_377585,RMVar_hsa_circ_203629 53784 RMVar_ID_53784 Human_SNP_ID_836508613 A-to-I Human chr2 + 26118223 26118223 26118223 TCGAACTCCTGACCTCATGGTCCGTCGTCCTCAGCCACCCAAAGTGCTGGGATTACAGGCGTGAG TCGAACTCCTGACCTCATGGTCCGTCGTCCTCGGCCACCCAAAGTGCTGGGATTACAGGCGTGAG A G RAB10 Ensembl:ENSG00000084733 Protein coding intron GSE38233 cultured B-cells chr2:26118222..26118223 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 UTCA 1 - RMVar_hsa_circ_57068,RMVar_hsa_circ_324091,RMVar_hsa_circ_197749,RMVar_hsa_circ_92976,RMVar_hsa_circ_197746,RMVar_hsa_circ_87850,RMVar_hsa_circ_197748 53785 RMVar_ID_53785 Human_SNP_ID_836521611 A-to-I Human chr2 - 200883536 200883536 200883536 TTGCCCAGGCTGGTCTTGAACTCCTGGACTCAAGTGATCTTCCTGCCTCCCAAAGTGCTGAGATT TTGCCCAGGCTGGTCTTGAACTCCTGGACTCATGTGATCTTCCTGCCTCCCAAAGTGCTGAGATT T A PPIL3 Ensembl:ENSG00000240344 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line chr2:200883535..200883536 23474544,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_17340,RMVar_hsa_circ_282766,RMVar_hsa_circ_108546,RMVar_hsa_circ_205830,RMVar_hsa_circ_205832 53786 RMVar_ID_53786 Human_SNP_ID_836571914 A-to-I Human chr2 - 38566185 38566185 38566185 TTTTGTATTTTTGTTAGAGACGGGGTTTCACCACGTTGGCCAGGCTGGTCTCGAACTCCTGGACC TTTTGTATTTTTGTTAGAGACGGGGTTTCACCGCGTTGGCCAGGCTGGTCTCGAACTCCTGGACC T C HNRNPLL Ensembl:ENSG00000143889 Protein coding intron GSE100210 HepG2 cell line chr2:38566184..38566185 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 7 haematopoietic and lymphoid tissue 53787 RMVar_ID_53787 Human_SNP_ID_836578964 A-to-I Human chr2 + 26285981 26285981 26285981 GCTAGTCTCGAATTGCCGACTTCAAGTGATCCACCCTCCTTGGCCTCCCAAAGTGCTGTGATTAC GCTAGTCTCGAATTGCCGACTTCAAGTGATCCCCCCTCCTTGGCCTCCCAAAGTGCTGTGATTAC A C HADHB Ensembl:ENSG00000138029 Protein coding intron GSE100210 HepG2 cell line chr2:26285980..26285981 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - RMVar_hsa_circ_197784,RMVar_hsa_circ_113033 53788 RMVar_ID_53788 Human_SNP_ID_836582259 A-to-I Human chr2 - 37103982 37103982 37103982 GTATCTGCCACCACTCCAGGTTAATTTTTTCTATTTTTAGTAGAGACGGAATTTCACCATGTTGA GTATCTGCCACCACTCCAGGTTAATTTTTTCTGTTTTTAGTAGAGACGGAATTTCACCATGTTGA T C EIF2AK2 Ensembl:ENSG00000055332 Protein coding 3'UTR GSE100210 HepG2 cell line chr2:37103981..37103982 29129909 RNA-Seq:(High) rs1464178248 Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 1 prostate Human_RBP_ID_6915977,Human_RBP_ID_26487092 53789 RMVar_ID_53789 Human_SNP_ID_836589252 A-to-I Human chr2 + 209180558 209180558 209180558 AAAGGCAGGGGCGACAGATCATCTCTGAAAGTAGTGAAGGCAGTAGCCCAGGTCTTGAATACATT AAAGGCAGGGGCGACAGATCATCTCTGAAAGTGGTGAAGGCAGTAGCCCAGGTCTTGAATACATT A G PKP4P1,MEAF6P1 Ensembl:ENSG00000229670,Ensembl:ENSG00000240286 Pseudogene,Pseudogene exon,intron GSE100210 HepG2 cell line chr2:209180557..209180558 29129909 RNA-Seq:(High) rs1306614702 Functional Loss SNV ICGC 33..33 33 LAML 2 - 53790 RMVar_ID_53790 Human_SNP_ID_836593562 A-to-I Human chr2 - 159539658 159539658 159539658 TTGCTGAGGCTGGTCTTGAACTCCTGGGCTCAAGCAGTCCTCTTATCTCAGCCTTTGACTCCAAG TTGCTGAGGCTGGTCTTGAACTCCTGGGCTCACGCAGTCCTCTTATCTCAGCCTTTGACTCCAAG T G BAZ2B Ensembl:ENSG00000123636 Protein coding intron GSE100210 HepG2 cell line chr2:159539657..159539658 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_72710,RMVar_hsa_circ_204084,RMVar_hsa_circ_312940,RMVar_hsa_circ_81141,RMVar_hsa_circ_204082,RMVar_hsa_circ_295892 53791 RMVar_ID_53791 Human_SNP_ID_836655758 A-to-I Human chr2 - 61532789 61532789 61532789 TGCTCTGTCACCAGGCCTGAGTGCAGTGGCACAGTCTCGGCTCACTGCAACCTCTGCCTCCCAGG TGCTCTGTCACCAGGCCTGAGTGCAGTGGCACTGTCTCGGCTCACTGCAACCTCTGCCTCCCAGG T A XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE38233 cultured B-cells chr2:61532788..61532789 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_13933397,Human_RBP_ID_22815943 RMVar_hsa_circ_315608,RMVar_hsa_circ_200502,RMVar_hsa_circ_302279,RMVar_hsa_circ_200514,RMVar_hsa_circ_296615,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_302621,RMVar_hsa_circ_316390,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_200543,RMVar_hsa_circ_308693,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_333365,RMVar_hsa_circ_200568,RMVar_hsa_circ_304877,RMVar_hsa_circ_200569,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_289892,RMVar_hsa_circ_98453,RMVar_hsa_circ_200581,RMVar_hsa_circ_326823,RMVar_hsa_circ_301783,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590,RMVar_hsa_circ_278039,RMVar_hsa_circ_200594,RMVar_hsa_circ_200595,RMVar_hsa_circ_18859,RMVar_hsa_circ_200593,RMVar_hsa_circ_200600,RMVar_hsa_circ_297031 53792 RMVar_ID_53792 Human_SNP_ID_836660211 A-to-I Human chr2 - 28867011 28867011 28867011 GAGGATTGCTGGAGGCTAGGAGTTCAAGACTAACCTGGCCAACATAGCAGGACCCCATCTTTATA GAGGATTGCTGGAGGCTAGGAGTTCAAGACTAGCCTGGCCAACATAGCAGGACCCCATCTTTATA T C TRMT61B Ensembl:ENSG00000171103 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr2:28867010..28867011 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - 53793 RMVar_ID_53793 Human_SNP_ID_836665441 A-to-I Human chr2 + 60903711 60903711 60903711 GTATACTACGCCTGGCTAATTTTTGTATTTTTATTAGACACAGGGTTTCACCATGTCAGCCAGCC GTATACTACGCCTGGCTAATTTTTGTATTTTTGTTAGACACAGGGTTTCACCATGTCAGCCAGCC A G REL Ensembl:ENSG00000162924 Protein coding intron GSE38233 cultured B-cells chr2:60903710..60903711 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_200201,RMVar_hsa_circ_265062,RMVar_hsa_circ_66548,RMVar_hsa_circ_72942,RMVar_hsa_circ_79042,RMVar_hsa_circ_98550,RMVar_hsa_circ_200200,RMVar_hsa_circ_352784,RMVar_hsa_circ_200204,RMVar_hsa_circ_348953,RMVar_hsa_circ_200205 53794 RMVar_ID_53794 Human_SNP_ID_836742491 A-to-I Human chr2 - 148021512 148021501 148021513 GATGTCTCCAGCCAGGGCCAAGCAGCAGCAGTAGCAGCAGCAGCAGTAGCAGCAGCAGCAGCAAC GATGTCTCCAGCCAGGGCCAAGCAGCAGCAG____________CAGTAGCAGCAGCAGCAGCAAC GCTGCTGCTGCTA G ORC4 Ensembl:ENSG00000115947 Protein coding 5'UTR GSE47997 K562 cells&HepG2 cells chr2:148021511..148021512 23474544 RNA-Seq:(High) rs1416304352 Functional Loss DEL TCGA 32..43 33 LIHC 1 - Human_Splice_Rec_304261,Human_Splice_Rec_304331 RMVar_hsa_circ_88979,RMVar_hsa_circ_203718 53795 RMVar_ID_53795 Human_SNP_ID_836753279 A-to-I Human chr2 - 33840102 33840102 33840102 AGGGTATTATCATCTACCGAGCCGCCTACTTCAGTATCTATGACACTGCAAAGGGAATGCTTCCG AGGGTATTATCATCTACCGAGCCGCCTACTTCGGTATCTATGACACTGCAAAGGGAATGCTTCCG T C SLC25A5P2 Ensembl:ENSG00000235064 Pseudogene exon GSE100210 HepG2 cell line chr2:33840101..33840102 29129909 RNA-Seq:(High) rs878987725 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_17393833,Human_RBP_ID_26482324 Human_miRNA_ID_1866562,Human_miRNA_ID_1866842 53796 RMVar_ID_53796 Human_SNP_ID_836768193 A-to-I Human chr2 + 207754767 207754767 207754767 TCAAGCCATCCTCTAGCCTCAGCCACACAAGTAGCTGGGACTACAAGTGCAACTGGCACCTGTCT TCAAGCCATCCTCTAGCCTCAGCCACACAAGTGGCTGGGACTACAAGTGCAACTGGCACCTGTCT A G CCNYL1 Ensembl:ENSG00000163249 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE107867 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;ASD brains,temporal_cortex chr2:207754766..207754767 23474544,24183664,29129909,30559470 RNA-Seq:(High) rs1413986919 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue RMVar_hsa_circ_206420,RMVar_hsa_circ_99464 53797 RMVar_ID_53797 Human_SNP_ID_836769045 A-to-I Human chr2 - 141743689 141743688 141743689 AGCCATGAGAAACTCCAAAACCAGAACATTTTATTACGGCTTTAGTGTTGTTGCTTGCTATTGAA AGCCATGAGAAACTCCAAAACCAGAACATTTT_TTACGGCTTTAGTGTTGTTGCTTGCTATTGAA AT A LRP1B Ensembl:ENSG00000168702 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank chr2:141743688..141743689 30559470 RNA-Seq:(High) - Functional Loss DEL ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_121478,RMVar_hsa_circ_203553,RMVar_hsa_circ_118491,RMVar_hsa_circ_203571,RMVar_hsa_circ_82511,RMVar_hsa_circ_203606,RMVar_hsa_circ_18654,RMVar_hsa_circ_77134,RMVar_hsa_circ_203611,RMVar_hsa_circ_203616,RMVar_hsa_circ_81775,RMVar_hsa_circ_377585,RMVar_hsa_circ_203629 53798 RMVar_ID_53798 Human_SNP_ID_836773053 A-to-I Human chr2 - 61528095 61528095 61528095 CAGTGAAACCCTGTCTCTACTGAAAATACAAAAATTAGCCAGGCGTGGTGGCAGGTGCCTGTAGT CAGTGAAACCCTGTCTCTACTGAAAATACAAAGATTAGCCAGGCGTGGTGGCAGGTGCCTGTAGT T C XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE38233 cultured B-cells chr2:61528094..61528095 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - RMVar_hsa_circ_315608,RMVar_hsa_circ_200502,RMVar_hsa_circ_302279,RMVar_hsa_circ_200514,RMVar_hsa_circ_296615,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_302621,RMVar_hsa_circ_316390,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_200543,RMVar_hsa_circ_308693,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_333365,RMVar_hsa_circ_200568,RMVar_hsa_circ_304877,RMVar_hsa_circ_200569,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_289892,RMVar_hsa_circ_98453,RMVar_hsa_circ_200581,RMVar_hsa_circ_326823,RMVar_hsa_circ_301783,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590,RMVar_hsa_circ_278039,RMVar_hsa_circ_200594,RMVar_hsa_circ_200595,RMVar_hsa_circ_18859,RMVar_hsa_circ_200593,RMVar_hsa_circ_200600,RMVar_hsa_circ_297031 53799 RMVar_ID_53799 Human_SNP_ID_836896119 A-to-I Human chr2 + 86143730 86143729 86143730 TCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCATTCGCCACCACGCCCA TCAAGCGATTCTCCTGCCTCAGCCTCCCGAGT_GCTGGGATTACAGGCATTCGCCACCACGCCCA TA T - - Other Unknown GSE100210 HepG2 cell line chr2:86143729..86143730 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 33..33 33 MELA 1 - 53800 RMVar_ID_53800 Human_SNP_ID_836902069 A-to-I Human chr2 - 28853714 28853714 28853714 GTCCTGCCTCAGCCTTCCCAGTAGCTGGGACTATAGGTGTGCACCACCACACCTGGCTAATTTTT GTCCTGCCTCAGCCTTCCCAGTAGCTGGGACTGTAGGTGTGCACCACCACACCTGGCTAATTTTT T C TRMT61B Ensembl:ENSG00000171103 Protein coding intron GSE38233 cultured B-cells chr2:28853713..28853714 24183664 RNA-Seq:(High) rs1207513340 Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_282561,RMVar_hsa_circ_271089,RMVar_hsa_circ_198127,RMVar_hsa_circ_198128,RMVar_hsa_circ_366187 53801 RMVar_ID_53801 Human_SNP_ID_836907703 A-to-I Human chr2 + 28909474 28909474 28909474 CTTCTTTTGTTCCTTACATCCTGTCTATTGTGAGTGTGTTTTGATTTGTTTGATTTGGCCTCTTT CTTCTTTTGTTCCTTACATCCTGTCTATTGTGGGTGTGTTTTGATTTGTTTGATTTGGCCTCTTT A G WDR43 Ensembl:ENSG00000163811 Protein coding intron GSE38233 cultured B-cells chr2:28909473..28909474 24183664 RNA-Seq:(High) rs13426929 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_2636413,Human_RBP_ID_3622573,Human_RBP_ID_6908571,Human_RBP_ID_23866535 RMVar_hsa_circ_99946,RMVar_hsa_circ_354345,RMVar_hsa_circ_356766,RMVar_hsa_circ_360567,RMVar_hsa_circ_341660,RMVar_hsa_circ_276733,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_198134,RMVar_hsa_circ_198132,RMVar_hsa_circ_288289,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_288307,RMVar_hsa_circ_269901,RMVar_hsa_circ_286168,RMVar_hsa_circ_111760,RMVar_hsa_circ_198137,RMVar_hsa_circ_198139,RMVar_hsa_circ_198140,RMVar_hsa_circ_198138,RMVar_hsa_circ_198136 53802 RMVar_ID_53802 Human_SNP_ID_837016018 A-to-I Human chr2 - 121347075 121347075 121347075 CTTAGTGGCAATTTATTCCGTAATCGGAGAAGACCTGAAACCTCACCTTGCACAGCTCACAGGGA CTTAGTGGCAATTTATTCCGTAATCGGAGAAGCCCTGAAACCTCACCTTGCACAGCTCACAGGGA T G CLASP1 Ensembl:ENSG00000074054 Protein coding CDS GSE100210 HepG2 cell line chr2:121347074..121347075 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 NKTL,haematopoietic_and_lymphoid_tissue NK-T_cell_lymphoma 7 haematopoietic and lymphoid tissue Human_RBP_ID_1896746,Human_RBP_ID_13593563,Human_RBP_ID_26820137 Human_Splice_Rec_293028,Human_Splice_Rec_293029,Human_Splice_Rec_293104,Human_Splice_Rec_293105,Human_Splice_Rec_293182,Human_Splice_Rec_293183,Human_Splice_Rec_293260,Human_Splice_Rec_293261,Human_Splice_Rec_293336,Human_Splice_Rec_293337,Human_Splice_Rec_293412,Human_Splice_Rec_293413,Human_Splice_Rec_293476,Human_Splice_Rec_293477 Human_miRNA_ID_2006340,Human_miRNA_ID_2696721 RMVar_hsa_circ_71907,RMVar_hsa_circ_315829,RMVar_hsa_circ_121713,RMVar_hsa_circ_202962,RMVar_hsa_circ_70155,RMVar_hsa_circ_202961 53803 RMVar_ID_53803 Human_SNP_ID_837056362 A-to-I Human chr2 - 159838892 159838892 159838892 ACTCAGAAGGCTGAGGCACCAGAATCACTTGAACCTGGGAGGTGGAGGTTGCAGTGAGCCGAGAT ACTCAGAAGGCTGAGGCACCAGAATCACTTGAGCCTGGGAGGTGGAGGTTGCAGTGAGCCGAGAT T C LY75-CD302,LY75 Ensembl:ENSG00000248672,Ensembl:ENSG00000054219 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells chr2:159838891..159838892 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_371112,RMVar_hsa_circ_204118 53804 RMVar_ID_53804 Human_SNP_ID_837066447 A-to-I Human chr2 + 203259791 203259791 203259791 TGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGAAGAATCGCTTGAACCTGGCTAATTTTTGTATT TGTAGTCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAACCTGGCTAATTTTTGTATT A G RN7SL670P,CYP20A1 Ensembl:ENSG00000264041,Ensembl:ENSG00000119004 Other,Protein coding exon,intron GSE100210 HepG2 cell line chr2:203259790..203259791 29129909 RNA-Seq:(High) rs371559509 Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 3 prostate RMVar_hsa_circ_149,RMVar_hsa_circ_63848,RMVar_hsa_circ_329379,RMVar_hsa_circ_342953,RMVar_hsa_circ_339158,RMVar_hsa_circ_301536,RMVar_hsa_circ_67078,RMVar_hsa_circ_206195,RMVar_hsa_circ_364805,RMVar_hsa_circ_74386,RMVar_hsa_circ_16446,RMVar_hsa_circ_43642,RMVar_hsa_circ_343130,RMVar_hsa_circ_8771,RMVar_hsa_circ_206198,RMVar_hsa_circ_206200,RMVar_hsa_circ_206202,RMVar_hsa_circ_206203,RMVar_hsa_circ_206201,RMVar_hsa_circ_206199 53805 RMVar_ID_53805 Human_SNP_ID_837161184 A-to-I Human chr2 + 156441522 156441522 156441522 TCAAGGCTGCAGTGAGCTGCGTTAGTGCCACTACGCTCCAGCCTGAGTGACAGAGCAAGACCTTG TCAAGGCTGCAGTGAGCTGCGTTAGTGCCACTTCGCTCCAGCCTGAGTGACAGAGCAAGACCTTG A T GPD2 Ensembl:ENSG00000115159 Protein coding intron GSE100210 HepG2 cell line chr2:156441521..156441522 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 53806 RMVar_ID_53806 Human_SNP_ID_837165671 A-to-I Human chr2 + 202397391 202397391 202397391 TAATATCTCCTTGAACCTTTAGAACTTGATCTATAGTCTCACTTAAGTAGATTACAGTAATAAGA TAATATCTCCTTGAACCTTTAGAACTTGATCTGTAGTCTCACTTAAGTAGATTACAGTAATAAGA A G BMPR2 Ensembl:ENSG00000204217 Protein coding intron GSE100210 HepG2 cell line chr2:202397390..202397391 29129909 RNA-Seq:(High) rs1469982577 Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_205980,RMVar_hsa_circ_108219 53807 RMVar_ID_53807 Human_SNP_ID_837201357 A-to-I Human chr2 - 47874167 47874167 47874167 CACTATCGTCCGGACTGGAGTGCAGTGGTGCAATCTCTGCTCACAGCAAGCTCCGCCTCCCAGGT CACTATCGTCCGGACTGGAGTGCAGTGGTGCAGTCTCTGCTCACAGCAAGCTCCGCCTCCCAGGT T C FBXO11 Ensembl:ENSG00000138081 Protein coding intron GSE100210 HepG2 cell line chr2:47874166..47874167 29129909 RNA-Seq:(High) rs902864161 Functional Loss SNV ICGC 33..33 33 RECA 1 - 53808 RMVar_ID_53808 Human_SNP_ID_837208859 A-to-I Human chr2 - 202846290 202846290 202846290 CAGAGCATAATGGCACTGCTGCACTCCAGCCTAGGCAACAGAGCAAGATCTTGTCTAAAAAAAAA CAGAGCATAATGGCACTGCTGCACTCCAGCCTGGGCAACAGAGCAAGATCTTGTCTAAAAAAAAA T C ICA1L Ensembl:ENSG00000163596 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr2:202846289..202846290 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 5 ovary RMVar_hsa_circ_206055,RMVar_hsa_circ_16061,RMVar_hsa_circ_206059,RMVar_hsa_circ_299585,RMVar_hsa_circ_317438,RMVar_hsa_circ_32960 53809 RMVar_ID_53809 Human_SNP_ID_837224531 A-to-I Human chr2 - 113709417 113709417 113709417 CCTTCCCTCACTCTTCTCAGCTATAAAGTGAGAAGCGAAATTCAGTATCTTTTAAGATTCCTCTC CCTTCCCTCACTCTTCTCAGCTATAAAGTGAGGAGCGAAATTCAGTATCTTTTAAGATTCCTCTC T C SLC35F5 Ensembl:ENSG00000115084 Protein coding intron GSE38233 cultured B-cells chr2:113709416..113709417 24183664 RNA-Seq:(High) rs935644 Functional Loss SNV ICGC 33..33 33 LAML 1 - GWAS_ID_3671,GWAS_ID_3672,GWAS_ID_3673,GWAS_ID_3674 53810 RMVar_ID_53810 Human_SNP_ID_837246530 A-to-I Human chr2 - 175945136 175945136 175945136 CCGGCACTTTGGGAGGCGGAGATGGGCAGATCACCTGAGGTCAGGAGTTCAAGACCAGCCTGACT CCGGCACTTTGGGAGGCGGAGATGGGCAGATCTCCTGAGGTCAGGAGTTCAAGACCAGCCTGACT T A LNPK Ensembl:ENSG00000144320 Protein coding intron GSE38233 cultured B-cells chr2:175945135..175945136 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_97582,RMVar_hsa_circ_67734,RMVar_hsa_circ_204803,RMVar_hsa_circ_329824,RMVar_hsa_circ_349472,RMVar_hsa_circ_124466,RMVar_hsa_circ_125585,RMVar_hsa_circ_107850,RMVar_hsa_circ_204804,RMVar_hsa_circ_204806,RMVar_hsa_circ_204807,RMVar_hsa_circ_204805 53811 RMVar_ID_53811 Human_SNP_ID_837323656 A-to-I Human chr2 + 10144547 10144547 10144547 TTGGGTCCAGCAGCTTTCTCAGTCCCAAACACATGTGACCTCACGATTCTGGCCCTTCCATGATC TTGGGTCCAGCAGCTTTCTCAGTCCCAAACACGTGTGACCTCACGATTCTGGCCCTTCCATGATC A G RRM2 Ensembl:ENSG00000171848 Protein coding intron GSE38233 cultured B-cells chr2:10144546..10144547 24183664 RNA-Seq:(High) rs12692399 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_1097685,Human_RBP_ID_14002199,Human_RBP_ID_18493174 53812 RMVar_ID_53812 Human_SNP_ID_837347163 A-to-I Human chr2 + 131130253 131130253 131130253 TTTTGTAGAGCTAGGATTTCACTATGTTGCCCAGGCTGGTCTTGAACTCCTGGGCTCAAGTGATC TTTTGTAGAGCTAGGATTTCACTATGTTGCCCTGGCTGGTCTTGAACTCCTGGGCTCAAGTGATC A T PLEKHB2 Ensembl:ENSG00000115762 Protein coding intron GSE100210 HepG2 cell line chr2:131130252..131130253 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_13611224 RMVar_hsa_circ_13672,RMVar_hsa_circ_107100,RMVar_hsa_circ_376122,RMVar_hsa_circ_203274,RMVar_hsa_circ_203278,RMVar_hsa_circ_301443,RMVar_hsa_circ_203276,RMVar_hsa_circ_305609,RMVar_hsa_circ_33415,RMVar_hsa_circ_299819,RMVar_hsa_circ_203279,RMVar_hsa_circ_117831,RMVar_hsa_circ_332134,RMVar_hsa_circ_203277,RMVar_hsa_circ_314213,RMVar_hsa_circ_203280,RMVar_hsa_circ_203281 53813 RMVar_ID_53813 Human_SNP_ID_837355397 A-to-I Human chr2 + 112561872 112561872 112561872 GTTTGTTTGTTTTGTAGAGATGGGGTCTTGCTATGTTATCCAGGCTGGTCTCGAACTCCTGGCCT GTTTGTTTGTTTTGTAGAGATGGGGTCTTGCTGTGTTATCCAGGCTGGTCTCGAACTCCTGGCCT A G POLR1B Ensembl:ENSG00000125630 Protein coding intron GSE38233 cultured B-cells chr2:112561871..112561872 24183664 RNA-Seq:(High) rs769187876 Functional Loss SNV ICGC 33..33 33 PRAD 1 - RMVar_hsa_circ_47061,RMVar_hsa_circ_326716,RMVar_hsa_circ_284203,RMVar_hsa_circ_82908,RMVar_hsa_circ_202659,RMVar_hsa_circ_72184,RMVar_hsa_circ_14682,RMVar_hsa_circ_344553,RMVar_hsa_circ_202664,RMVar_hsa_circ_48357,RMVar_hsa_circ_87156,RMVar_hsa_circ_373003,RMVar_hsa_circ_202665 53814 RMVar_ID_53814 Human_SNP_ID_837363106 A-to-I Human chr2 + 216503534 216503534 216503534 CTCGTGCCTCAGCCTCCGAAGTAGCTGGGATTACAGGCTTATGCCACAAAGCTCAGCTAGTTTTT CTCGTGCCTCAGCCTCCGAAGTAGCTGGGATTGCAGGCTTATGCCACAAAGCTCAGCTAGTTTTT A G RPL37A Ensembl:ENSG00000197756 Protein coding 3'UTR GSE38233 cultured B-cells chr2:216503533..216503534 24183664 RNA-Seq:(High) rs1470390933 Functional Loss SNV ICGC 33..33 33 PBCA 1 - 53815 RMVar_ID_53815 Human_SNP_ID_837364423 A-to-I Human chr2 - 218547260 218547260 218547260 CAGTGGTACAGTTGTAGCTCACTATAACCTCAAACTATTGAGCTCAAGTGATCCTCCCGCCTTCG CAGTGGTACAGTTGTAGCTCACTATAACCTCAGACTATTGAGCTCAAGTGATCCTCCCGCCTTCG T C USP37 Ensembl:ENSG00000135913 Protein coding intron GSE100210 HepG2 cell line chr2:218547259..218547260 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_104950,RMVar_hsa_circ_206934,RMVar_hsa_circ_359894,RMVar_hsa_circ_60414,RMVar_hsa_circ_12241,RMVar_hsa_circ_274891,RMVar_hsa_circ_15303,RMVar_hsa_circ_40773,RMVar_hsa_circ_34886,RMVar_hsa_circ_266541,RMVar_hsa_circ_371770,RMVar_hsa_circ_28618,RMVar_hsa_circ_27333,RMVar_hsa_circ_28284,RMVar_hsa_circ_206954,RMVar_hsa_circ_206955,RMVar_hsa_circ_350978,RMVar_hsa_circ_23734,RMVar_hsa_circ_357240,RMVar_hsa_circ_47380,RMVar_hsa_circ_280371,RMVar_hsa_circ_378790,RMVar_hsa_circ_206962,RMVar_hsa_circ_206960,RMVar_hsa_circ_297632,RMVar_hsa_circ_272922,RMVar_hsa_circ_356060,RMVar_hsa_circ_322842,RMVar_hsa_circ_40513,RMVar_hsa_circ_71427,RMVar_hsa_circ_206969,RMVar_hsa_circ_206970,RMVar_hsa_circ_73078,RMVar_hsa_circ_290607,RMVar_hsa_circ_318764,RMVar_hsa_circ_206974,RMVar_hsa_circ_206972,RMVar_hsa_circ_206973,RMVar_hsa_circ_272670,RMVar_hsa_circ_354375,RMVar_hsa_circ_364690,RMVar_hsa_circ_324827,RMVar_hsa_circ_206975 53816 RMVar_ID_53816 Human_SNP_ID_837369135 A-to-I Human chr2 - 37106861 37106861 37106861 TTTTGTGTTTTTAATAAAGACAGGGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTCCTGACCT TTTTGTGTTTTTAATAAAGACAGGGTTTCACCGTGTTGGCCAGGCTGGTCTCAAACTCCTGACCT T C EIF2AK2 Ensembl:ENSG00000055332 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells chr2:37106860..37106861 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_145650 53817 RMVar_ID_53817 Human_SNP_ID_837376012 A-to-I Human chr2 + 143013019 143013019 143013019 TCTTATTAATTTTTTAGAGACAAAGTCTCACTATGTTGTCCAGGCTGGAGTGTGATGGCTATTCA TCTTATTAATTTTTTAGAGACAAAGTCTCACTGTGTTGTCCAGGCTGGAGTGTGATGGCTATTCA A G KYNU Ensembl:ENSG00000115919 Protein coding intron GSE100210 HepG2 cell line chr2:143013018..143013019 29129909 RNA-Seq:(High) rs967948875 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_13629772 RMVar_hsa_circ_203643,RMVar_hsa_circ_84672 53818 RMVar_ID_53818 Human_SNP_ID_837411007 A-to-I Human chr2 + 209180812 209180812 209180812 ATATTCCTCACCAGCAAGAGAACTAAATAGACAGCTACAGCATCAACAGCTGTATTATAGTCAAG ATATTCCTCACCAGCAAGAGAACTAAATAGACGGCTACAGCATCAACAGCTGTATTATAGTCAAG A G PKP4P1,MEAF6P1 Ensembl:ENSG00000229670,Ensembl:ENSG00000240286 Pseudogene,Pseudogene exon,intron GSE100210 HepG2 cell line chr2:209180811..209180812 29129909 RNA-Seq:(High) rs1431219311 Functional Loss SNV ICGC 33..33 33 LAML 2 - 53819 RMVar_ID_53819 Human_SNP_ID_837467996 A-to-I Human chr2 - 50610996 50610996 50610996 CATGCCTGTAGTCCCAGCACTGCAGGAGGCCAAGTCAGGTAGATGACTTGAAATCAGGAGTTCAA CATGCCTGTAGTCCCAGCACTGCAGGAGGCCAGGTCAGGTAGATGACTTGAAATCAGGAGTTCAA T C NRXN1 Ensembl:ENSG00000179915 Protein coding intron GSE107867 ASD brains,frontal_cortex chr2:50610995..50610996 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_6943,RMVar_hsa_circ_36864,RMVar_hsa_circ_294728,RMVar_hsa_circ_307129,RMVar_hsa_circ_268420,RMVar_hsa_circ_292093,RMVar_hsa_circ_327433,RMVar_hsa_circ_268933,RMVar_hsa_circ_329013,RMVar_hsa_circ_279431,RMVar_hsa_circ_295343,RMVar_hsa_circ_308859,RMVar_hsa_circ_312149,RMVar_hsa_circ_326022,RMVar_hsa_circ_7426,RMVar_hsa_circ_35984,RMVar_hsa_circ_377042,RMVar_hsa_circ_265207,RMVar_hsa_circ_279154,RMVar_hsa_circ_199764,RMVar_hsa_circ_199765,RMVar_hsa_circ_320755,RMVar_hsa_circ_346070 53820 RMVar_ID_53820 Human_SNP_ID_837496169 A-to-I Human chr2 + 44402069 44402069 44402069 ATAGAATTGGCCGGGCGCGGTGGCTCACGCCTATAGTCCCAGGACTTTGGGAGGCCAAGGCGGGT ATAGAATTGGCCGGGCGCGGTGGCTCACGCCTGTAGTCCCAGGACTTTGGGAGGCCAAGGCGGGT A G CAMKMT Ensembl:ENSG00000143919 Protein coding intron GSE100210 HepG2 cell line chr2:44402068..44402069 29129909 RNA-Seq:(High) rs542672062 Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 5 pancreas RMVar_hsa_circ_7903 53821 RMVar_ID_53821 Human_SNP_ID_837556058 A-to-I Human chr2 - 113843282 113843281 113843282 TCTTACCCAGAATCAATCACACTGGGACACTGAAAAAAAAAAAAAAGGAAAGTAAGTAGAGTCAG TCTTACCCAGAATCAATCACACTGGGACACTG_AAAAAAAAAAAAAGGAAAGTAAGTAGAGTCAG TT T AC104653.1 Ensembl:ENSG00000228857 lincRNA exon GSE38233 cultured B-cells chr2:113843282..113843283 24183664 RNA-Seq:(High) - Functional Loss DEL ICGC 33..33 33 LMS 1 - Human_Splice_Rec_290791 RMVar_hsa_circ_202733,RMVar_hsa_circ_202734 53822 RMVar_ID_53822 Human_SNP_ID_837591814 A-to-I Human chr2 + 9854147 9854147 9854147 AGTGTGCATTTTGTGGAACTCAATGTTCTGATAGATGCTACATACAGACCCCAGAGATTTTGTTC AGTGTGCATTTTGTGGAACTCAATGTTCTGATGGATGCTACATACAGACCCCAGAGATTTTGTTC A G TAF1B Ensembl:ENSG00000115750 Protein coding intron GSE100210 HepG2 cell line chr2:9854146..9854147 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue Human_RBP_ID_1241512 RMVar_hsa_circ_8469,RMVar_hsa_circ_16824,RMVar_hsa_circ_360092,RMVar_hsa_circ_370697,RMVar_hsa_circ_277698,RMVar_hsa_circ_50264,RMVar_hsa_circ_40124,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 53823 RMVar_ID_53823 Human_SNP_ID_837642791 A-to-I Human chr2 - 216610929 216610929 216610929 TCATGTCTATTATGTCCTATAACGGAGGAGCCATCATGGCCATGAAGGGGAAGAACCGTGTGGCC TCATGTCTATTATGTCCTATAACGGAGGAGCCGTCATGGCCATGAAGGGGAAGAACCGTGTGGCC T C PSMB3P2 Ensembl:ENSG00000235444 Pseudogene exon GSE100210 HepG2 cell line chr2:216610928..216610929 29129909 RNA-Seq:(High) rs1351516850 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_miRNA_ID_1839059,Human_miRNA_ID_1855166 53824 RMVar_ID_53824 Human_SNP_ID_837644836 A-to-I Human chr2 + 101704762 101704762 101704762 TTGTATTTTTAGTAGAGATGGGGTTTCACCATATTGGCCAGGCTGGTCTCGAACTCGAGTCAGGG TTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAACTCGAGTCAGGG A G MAP4K4 Ensembl:ENSG00000071054 Protein coding intron GSE100210 HepG2 cell line chr2:101704761..101704762 29129909 RNA-Seq:(High) rs1390953864 Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 33 prostate RMVar_hsa_circ_13472,RMVar_hsa_circ_27514,RMVar_hsa_circ_340358,RMVar_hsa_circ_22836,RMVar_hsa_circ_97038,RMVar_hsa_circ_12605,RMVar_hsa_circ_202260 53825 RMVar_ID_53825 Human_SNP_ID_837652548 A-to-I Human chr2 - 131089170 131089170 131089170 CCTGAGGTCGGAAGTTCGAGACCAACCTGACCAACGTGGAGAAACCCCGTCTCTACTAAAAATAC CCTGAGGTCGGAAGTTCGAGACCAACCTGACCGACGTGGAGAAACCCCGTCTCTACTAAAAATAC T C FAM168B Ensembl:ENSG00000152102 Protein coding intron GSE100210 HepG2 cell line chr2:131089169..131089170 29129909 RNA-Seq:(High) rs1212558379 Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_88391,RMVar_hsa_circ_203265,RMVar_hsa_circ_346190,RMVar_hsa_circ_303327 53826 RMVar_ID_53826 Human_SNP_ID_837679519 A-to-I Human chr2 - 159604304 159604304 159604304 CAGGAGTGTGAGACCAGCCAGAGCAACATAGTAAGACTCCTACCTCTAAAAATAAAATAAAATAT CAGGAGTGTGAGACCAGCCAGAGCAACATAGTTAGACTCCTACCTCTAAAAATAAAATAAAATAT T A BAZ2B Ensembl:ENSG00000123636 Protein coding intron GSE100210 HepG2 cell line chr2:159604303..159604304 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_72710,RMVar_hsa_circ_81141,RMVar_hsa_circ_204082,RMVar_hsa_circ_204087 53827 RMVar_ID_53827 Human_SNP_ID_837683407 A-to-I Human chr2 + 73524509 73524509 73524509 ATGGAGTCTTGCTCTGTCACCCAGGCTGGAGTACAGTGGCATGATCTCAGCTCACTGCAACCTCT ATGGAGTCTTGCTCTGTCACCCAGGCTGGAGTGCAGTGGCATGATCTCAGCTCACTGCAACCTCT A G ALMS1 Ensembl:ENSG00000116127 Protein coding intron GSE47997 K562 cells&HepG2 cells chr2:73524508..73524509 23474544 RNA-Seq:(High) rs1235517683 Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 3 prostate RMVar_hsa_circ_2627,RMVar_hsa_circ_363390,RMVar_hsa_circ_65798,RMVar_hsa_circ_364347,RMVar_hsa_circ_348169,RMVar_hsa_circ_59297,RMVar_hsa_circ_24066,RMVar_hsa_circ_64287,RMVar_hsa_circ_376441,RMVar_hsa_circ_69522,RMVar_hsa_circ_80133,RMVar_hsa_circ_311178,RMVar_hsa_circ_361113,RMVar_hsa_circ_201231,RMVar_hsa_circ_201232 53828 RMVar_ID_53828 Human_SNP_ID_837703668 A-to-I Human chr2 - 197432063 197432063 197432063 TTGGAGTGCAGTGGCGTGATCATAGCTCACTTAACCTACAACTGCTGGGCTCAAGTGATCCTCCC TTGGAGTGCAGTGGCGTGATCATAGCTCACTTTACCTACAACTGCTGGGCTCAAGTGATCCTCCC T A SF3B1 Ensembl:ENSG00000115524 Protein coding intron GSE38233 cultured B-cells chr2:197432062..197432063 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 5 liver RMVar_hsa_circ_205657,RMVar_hsa_circ_98855 53829 RMVar_ID_53829 Human_SNP_ID_837710871 A-to-I Human chr2 - 50444919 50444919 50444919 ATTTAAGGGGGAACCAAAAAGCTCAGTAATCAAGATAAATTATATTTTACTGCAATATTTGAAAA ATTTAAGGGGGAACCAAAAAGCTCAGTAATCAGGATAAATTATATTTTACTGCAATATTTGAAAA T C NRXN1 Ensembl:ENSG00000179915 Protein coding intron GSE107867 ASD brains,frontal_cortex chr2:50444918..50444919 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_6943,RMVar_hsa_circ_17909,RMVar_hsa_circ_275756,RMVar_hsa_circ_309080,RMVar_hsa_circ_36864,RMVar_hsa_circ_16483,RMVar_hsa_circ_291180,RMVar_hsa_circ_294728,RMVar_hsa_circ_293440,RMVar_hsa_circ_321005,RMVar_hsa_circ_307129,RMVar_hsa_circ_301810,RMVar_hsa_circ_268420,RMVar_hsa_circ_292093,RMVar_hsa_circ_309127,RMVar_hsa_circ_323678,RMVar_hsa_circ_327433,RMVar_hsa_circ_318918,RMVar_hsa_circ_289804 53830 RMVar_ID_53830 Human_SNP_ID_837744094 A-to-I Human chr2 + 44228383 44228383 44228383 TTTTGTAGAGATAGGGTCTCATTGTGTTTCCCAGGCTGGCCTAGAACTCCTGACCTCAAGGAATC TTTTGTAGAGATAGGGTCTCATTGTGTTTCCCGGGCTGGCCTAGAACTCCTGACCTCAAGGAATC A G PPM1B,AC013717.1 Ensembl:ENSG00000138032,Ensembl:ENSG00000285542 Protein coding,Protein coding intron,intron GSE107867 ASD brains,frontal_cortex chr2:44228382..44228383 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_13895775 RMVar_hsa_circ_92064,RMVar_hsa_circ_199468 53831 RMVar_ID_53831 Human_SNP_ID_838033571 A-to-I Human chr2 - 127843863 127843863 127843863 CCTCTAGCAGTCCACCTGTTTCCGCCTCCCAAATGCTGAGATTAGAGGCATGAGTCACTGCACCC CCTCTAGCAGTCCACCTGTTTCCGCCTCCCAACTGCTGAGATTAGAGGCATGAGTCACTGCACCC T G POLR2D Ensembl:ENSG00000144231 Protein coding 3'UTR GSE100210 HepG2 cell line chr2:127843862..127843863 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 3 uterus 53832 RMVar_ID_53832 Human_SNP_ID_838052432 A-to-I Human chr2 + 131500504 131500504 131500504 CTGTTTTTGTTTGTTTGTTCAATTTCATGTTCAGTGGCCCAATGATGAAGTTGGTTTATAAGCTT CTGTTTTTGTTTGTTTGTTCAATTTCATGTTCTGTGGCCCAATGATGAAGTTGGTTTATAAGCTT A T SMPD4BP Ensembl:ENSG00000152117 Pseudogene intron GSE105773 Glioblastoma cells,U87MG chr2:131500503..131500504 29724793 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC 33..33 33 LUSC 2 - Human_Splice_Rec_298387,Human_Splice_Rec_298423 RMVar_hsa_circ_22820,RMVar_hsa_circ_52405,RMVar_hsa_circ_12883,RMVar_hsa_circ_343371,RMVar_hsa_circ_345607,RMVar_hsa_circ_112946 53833 RMVar_ID_53833 Human_SNP_ID_838128103 A-to-I Human chr2 + 134949895 134949895 134949895 TCGGCTCGCTGCACCCTCCGCCTCCCGGGTTCAAGCAGTTCTCTGCCTCAGCCTCCTGAGTAGCT TCGGCTCGCTGCACCCTCCGCCTCCCGGGTTCCAGCAGTTCTCTGCCTCAGCCTCCTGAGTAGCT A C CCNT2 Ensembl:ENSG00000082258 Protein coding intron GSE100210 HepG2 cell line chr2:134949895..134949896 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_13614861 RMVar_hsa_circ_224,RMVar_hsa_circ_359432,RMVar_hsa_circ_203357,RMVar_hsa_circ_83299,RMVar_hsa_circ_203363,RMVar_hsa_circ_57271 53834 RMVar_ID_53834 Human_SNP_ID_838146281 A-to-I Human chr2 - 33839979 33839979 33839979 TTGCTGGGTTGACTTCCTATCCATTTGACACCATTCGCCACCACATGATGATGCAGTCAGGGTGC TTGCTGGGTTGACTTCCTATCCATTTGACACCGTTCGCCACCACATGATGATGCAGTCAGGGTGC T C SLC25A5P2 Ensembl:ENSG00000235064 Pseudogene exon GSE100210 HepG2 cell line chr2:33839978..33839979 29129909 RNA-Seq:(High) rs796462576 Functional Loss SNV ICGC 33..33 33 COCA 4 - Human_miRNA_ID_1905164 53835 RMVar_ID_53835 Human_SNP_ID_838181109 A-to-I Human chr2 + 237106338 237106338 237106338 TAGTTAACAAAACATATTGCATAGTTTCAGATAGCTAGAAGGAGTTTATTAAATGTTCCCAATAC TAGTTAACAAAACATATTGCATAGTTTCAGATGGCTAGAAGGAGTTTATTAAATGTTCCCAATAC A G - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr2:237106337..237106338 30559470 RNA-Seq:(High) rs906904217 Functional Loss SNV ICGC 33..33 33 BRCA 1 - Human_RBP_ID_23859136 53836 RMVar_ID_53836 Human_SNP_ID_838234745 A-to-I Human chr2 + 202564895 202564895 202564895 GATGAAACCTCATCTCTACTAAAAATACAAATAATTAGCCAGGCATGGTGGCACGCGCCTGTAGT GATGAAACCTCATCTCTACTAAAAATACAAATGATTAGCCAGGCATGGTGGCACGCGCCTGTAGT A G BMPR2 Ensembl:ENSG00000204217 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells chr2:202564894..202564895 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_268125,RMVar_hsa_circ_265461 53837 RMVar_ID_53837 Human_SNP_ID_838263392 A-to-I Human chr2 + 10128671 10128671 10128671 AGGGTCTTGAATGGGACTGAGCTTGCCTTGGTAGTGACATCAGCAGAGAAGTCAGTAGTTGAAGT AGGGTCTTGAATGGGACTGAGCTTGCCTTGGTGGTGACATCAGCAGAGAAGTCAGTAGTTGAAGT A G RRM2 Ensembl:ENSG00000171848 Protein coding intron GSE38233 cultured B-cells chr2:10128670..10128671 24183664 RNA-Seq:(High) rs4668664 Functional Loss SNV ICGC 33..33 33 ESCA 1 - GWAS_ID_1984,GWAS_ID_1985,GWAS_ID_1986,GWAS_ID_1987 RMVar_hsa_circ_12142,RMVar_hsa_circ_65270,RMVar_hsa_circ_371954,RMVar_hsa_circ_196929,RMVar_hsa_circ_106923,RMVar_hsa_circ_18516,RMVar_hsa_circ_117641,RMVar_hsa_circ_196933,RMVar_hsa_circ_196934 53838 RMVar_ID_53838 Human_SNP_ID_838306117 A-to-I Human chr2 - 49229761 49229761 49229761 CCACCGGCGTCAAAGTATTTAGCTGACTCGCTACACTCCACGGAAGCAATATGAAGTGATCTGCT CCACCGGCGTCAAAGTATTTAGCTGACTCGCTGCACTCCACGGAAGCAATATGAAGTGATCTGCT T C AC009975.2 Ensembl:ENSG00000282998 lincRNA intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr2:49229761..49229762 30559470 RNA-Seq:(High) rs983287243 Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_20437967 53839 RMVar_ID_53839 Human_SNP_ID_838324504 A-to-I Human chr2 + 138288057 138288057 138288057 CTCCCTGATTTTTGTCTTCCACGTCCTGCAGCACTTCTTTATTCTGCTCTTCACCATCACCCTGC CTCCCTGATTTTTGTCTTCCACGTCCTGCAGCGCTTCTTTATTCTGCTCTTCACCATCACCCTGC A G - - Other Unknown GSE100210 HepG2 cell line chr2:138288056..138288057 29129909 RNA-Seq:(High) rs879017332 Functional Loss SNV ICGC 33..33 33 LAML 1 - 53840 RMVar_ID_53840 Human_SNP_ID_838344592 A-to-I Human chr2 + 169752759 169752759 169752759 TGAAGTCACTGCGGTATGATGAAAAATATTTTACTAAGGCCAAACATTTTAGTAATCCCAGCCTG TGAAGTCACTGCGGTATGATGAAAAATATTTTGCTAAGGCCAAACATTTTAGTAATCCCAGCCTG A G KLHL23 Ensembl:ENSG00000213160 Protein coding intron GSE38233 cultured B-cells chr2:169752758..169752759 24183664 RNA-Seq:(High) rs10171909 Functional Loss SNV ICGC 33..33 33 ESCA 1 - 53841 RMVar_ID_53841 Human_SNP_ID_838401376 A-to-I Human chr2 + 203117794 203117794 203117794 GTCTTGAACTCCTGAGCTTAAGTAGTCCTCCCACCTTCAGTCTCCGGAGTAGCTAGGACTACAGG GTCTTGAACTCCTGAGCTTAAGTAGTCCTCCCCCCTTCAGTCTCCGGAGTAGCTAGGACTACAGG A C NBEAL1 Ensembl:ENSG00000144426 Protein coding intron GSE100210 HepG2 cell line chr2:203117793..203117794 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_3397,RMVar_hsa_circ_104425,RMVar_hsa_circ_79681,RMVar_hsa_circ_83224,RMVar_hsa_circ_206102,RMVar_hsa_circ_206103,RMVar_hsa_circ_206101,RMVar_hsa_circ_11727,RMVar_hsa_circ_54883,RMVar_hsa_circ_206110,RMVar_hsa_circ_104377,RMVar_hsa_circ_124661,RMVar_hsa_circ_5335,RMVar_hsa_circ_9626,RMVar_hsa_circ_206118,RMVar_hsa_circ_115690,RMVar_hsa_circ_78980,RMVar_hsa_circ_54727,RMVar_hsa_circ_206120,RMVar_hsa_circ_51416,RMVar_hsa_circ_206121,RMVar_hsa_circ_47774,RMVar_hsa_circ_80575,RMVar_hsa_circ_206128,RMVar_hsa_circ_364407,RMVar_hsa_circ_21150,RMVar_hsa_circ_31562,RMVar_hsa_circ_10409,RMVar_hsa_circ_73313,RMVar_hsa_circ_294598,RMVar_hsa_circ_342918,RMVar_hsa_circ_354382,RMVar_hsa_circ_369656,RMVar_hsa_circ_378947,RMVar_hsa_circ_366441,RMVar_hsa_circ_351875,RMVar_hsa_circ_351934,RMVar_hsa_circ_343763,RMVar_hsa_circ_330115,RMVar_hsa_circ_332324,RMVar_hsa_circ_94708,RMVar_hsa_circ_84293,RMVar_hsa_circ_206133,RMVar_hsa_circ_206135,RMVar_hsa_circ_51465,RMVar_hsa_circ_206134,RMVar_hsa_circ_206131,RMVar_hsa_circ_206132,RMVar_hsa_circ_326021,RMVar_hsa_circ_206130,RMVar_hsa_circ_206138,RMVar_hsa_circ_206141,RMVar_hsa_circ_331071,RMVar_hsa_circ_343440,RMVar_hsa_circ_206142 53842 RMVar_ID_53842 Human_SNP_ID_838424789 A-to-I Human chr2 + 9450926 9450926 9450926 AAAACTTAGGGTATGAGGTTTTTGTTGTAAATAGTCGTAGTTACTCCTGAGTCTTACTGTCCACA AAAACTTAGGGTATGAGGTTTTTGTTGTAAATGGTCGTAGTTACTCCTGAGTCTTACTGTCCACA A G CPSF3 Ensembl:ENSG00000119203 Protein coding intron GSE38233 cultured B-cells chr2:9450925..9450926 24183664 RNA-Seq:(High) rs6705033 Functional Loss SNV ICGC 33..33 33 ESCA 1 - GWAS_ID_1980,GWAS_ID_1981,GWAS_ID_1982,GWAS_ID_1983 RMVar_hsa_circ_118941,RMVar_hsa_circ_196859,RMVar_hsa_circ_107887,RMVar_hsa_circ_196860,RMVar_hsa_circ_13109,RMVar_hsa_circ_77677,RMVar_hsa_circ_196867,RMVar_hsa_circ_196868,RMVar_hsa_circ_371619,RMVar_hsa_circ_373941,RMVar_hsa_circ_26490,RMVar_hsa_circ_43012,RMVar_hsa_circ_110741,RMVar_hsa_circ_196870,RMVar_hsa_circ_196871,RMVar_hsa_circ_377354,RMVar_hsa_circ_11181,RMVar_hsa_circ_68155,RMVar_hsa_circ_196873,RMVar_hsa_circ_70594,RMVar_hsa_circ_196875,RMVar_hsa_circ_105068,RMVar_hsa_circ_116674,RMVar_hsa_circ_196876,RMVar_hsa_circ_41462,RMVar_hsa_circ_345013,RMVar_hsa_circ_358810,RMVar_hsa_circ_313191,RMVar_hsa_circ_196878 53843 RMVar_ID_53843 Human_SNP_ID_838440943 A-to-I Human chr2 + 231165879 231165879 231165879 CTTTTTTTAAATTTTATTTTATAGGATGAGGCAGAGAAAAAGGAGGAAAAAGAGAAGAAAAAAGA CTTTTTTTAAATTTTATTTTATAGGATGAGGCGGAGAAAAAGGAGGAAAAAGAGAAGAAAAAAGA A G PSMD1 Ensembl:ENSG00000173692 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr2:231165878..231165879 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_9096,Human_RBP_ID_60327,Human_RBP_ID_2626856,Human_RBP_ID_22998796,Human_RBP_ID_24546565,Human_RBP_ID_25586835,Human_RBP_ID_26340332,Human_RBP_ID_27818037 Human_Splice_Rec_369436,Human_Splice_Rec_369524,Human_Splice_Rec_369580,Human_Splice_Rec_369624,Human_Splice_Rec_369652 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 53844 RMVar_ID_53844 Human_SNP_ID_838453512 A-to-I Human chr2 + 45868766 45868766 45868766 CAAGACCAGCCTGGCCAACATGGGGAAACCCCATCTCTACTAAAAATACAAAAAATAAAATAAAA CAAGACCAGCCTGGCCAACATGGGGAAACCCCCTCTCTACTAAAAATACAAAAAATAAAATAAAA A C PRKCE Ensembl:ENSG00000171132 Protein coding intron GSE47997 K562 cells&HepG2 cells chr2:45868765..45868766 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - RMVar_hsa_circ_28332,RMVar_hsa_circ_27698 53845 RMVar_ID_53845 Human_SNP_ID_838523789 A-to-I Human chr2 + 85539201 85539201 85539201 TTCGCTCCGCGCCGCCCGCCTGCTACGAGTAGAACGCTGTCCGCAGCTTGCGCATTTCGCAGCCG TTCGCTCCGCGCCGCCCGCCTGCTACGAGTAGGACGCTGTCCGCAGCTTGCGCATTTCGCAGCCG A G MAT2A Ensembl:ENSG00000168906 Protein coding exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr2:85539201..85539202 30559470 RNA-Seq:(High) rs989401149 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_243153,Human_RBP_ID_776449,Human_RBP_ID_829804,Human_RBP_ID_1590932,Human_RBP_ID_1924048,Human_RBP_ID_2666982,Human_RBP_ID_3635416,Human_RBP_ID_4634866,Human_RBP_ID_5445178,Human_RBP_ID_5589626,Human_RBP_ID_13972934,Human_RBP_ID_18766450 RMVar_hsa_circ_91716,RMVar_hsa_circ_201547 53846 RMVar_ID_53846 Human_SNP_ID_838559128 A-to-I Human chr2 - 86064208 86064208 86064208 GAAACCAGACTAACCCACAAACAAATTCTTGCATAGTGTAGTCACTCTTGCCCTTTTCACCTGTT GAAACCAGACTAACCCACAAACAAATTCTTGCGTAGTGTAGTCACTCTTGCCCTTTTCACCTGTT T C POLR1A Ensembl:ENSG00000068654 Protein coding intron GSE38233 cultured B-cells chr2:86064207..86064208 24183664 RNA-Seq:(High) rs1386040055 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 3 liver 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 53847 RMVar_ID_53847 Human_SNP_ID_838561110 A-to-I Human chr2 + 135656978 135656978 135656978 AAAATTAGCCGGACCTGGTGGTGGGTGCCTATAATCCCAGCTGCCTTGGGAGGCTGAGGCACAAG AAAATTAGCCGGACCTGGTGGTGGGTGCCTATGATCCCAGCTGCCTTGGGAGGCTGAGGCACAAG A G R3HDM1 Ensembl:ENSG00000048991 Protein coding intron GSE100210 HepG2 cell line chr2:135656978..135656979 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 6 pancreas RMVar_hsa_circ_203406,RMVar_hsa_circ_97196,RMVar_hsa_circ_309589,RMVar_hsa_circ_313853,RMVar_hsa_circ_50693,RMVar_hsa_circ_203408,RMVar_hsa_circ_375158,RMVar_hsa_circ_379103,RMVar_hsa_circ_353778,RMVar_hsa_circ_203426,RMVar_hsa_circ_320654,RMVar_hsa_circ_81201,RMVar_hsa_circ_297511,RMVar_hsa_circ_34570,RMVar_hsa_circ_203431,RMVar_hsa_circ_203432,RMVar_hsa_circ_203430,RMVar_hsa_circ_283944,RMVar_hsa_circ_284866,RMVar_hsa_circ_203437,RMVar_hsa_circ_203434,RMVar_hsa_circ_203435,RMVar_hsa_circ_365020,RMVar_hsa_circ_375962,RMVar_hsa_circ_203438,RMVar_hsa_circ_60843,RMVar_hsa_circ_126534,RMVar_hsa_circ_108309,RMVar_hsa_circ_203439,RMVar_hsa_circ_203442,RMVar_hsa_circ_373448,RMVar_hsa_circ_311528,RMVar_hsa_circ_203443,RMVar_hsa_circ_320581,RMVar_hsa_circ_305680,RMVar_hsa_circ_9114,RMVar_hsa_circ_203445,RMVar_hsa_circ_13702,RMVar_hsa_circ_203446,RMVar_hsa_circ_337701,RMVar_hsa_circ_203444,RMVar_hsa_circ_283601,RMVar_hsa_circ_203448 53848 RMVar_ID_53848 Human_SNP_ID_838599419 A-to-I Human chr2 + 48484070 48484070 48484070 AAAACAAACTTTGACGCCATAACAAAAATCATAGGCTGTGACTCCTGTAGCCACCCACACATTCC AAAACAAACTTTGACGCCATAACAAAAATCATTGGCTGTGACTCCTGTAGCCACCCACACATTCC A T PPP1R21 Ensembl:ENSG00000162869 Protein coding intron GSE100210 HepG2 cell line chr2:48484069..48484070 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - RMVar_hsa_circ_328020,RMVar_hsa_circ_284081,RMVar_hsa_circ_281781,RMVar_hsa_circ_30179,RMVar_hsa_circ_44269,RMVar_hsa_circ_73510,RMVar_hsa_circ_199694,RMVar_hsa_circ_199695,RMVar_hsa_circ_57601,RMVar_hsa_circ_32365,RMVar_hsa_circ_51467,RMVar_hsa_circ_68225,RMVar_hsa_circ_368582,RMVar_hsa_circ_266661,RMVar_hsa_circ_341793,RMVar_hsa_circ_287366,RMVar_hsa_circ_199705,RMVar_hsa_circ_199706,RMVar_hsa_circ_199714,RMVar_hsa_circ_301505,RMVar_hsa_circ_314976,RMVar_hsa_circ_320381,RMVar_hsa_circ_334042,RMVar_hsa_circ_373127,RMVar_hsa_circ_308622,RMVar_hsa_circ_82826,RMVar_hsa_circ_272373,RMVar_hsa_circ_199710,RMVar_hsa_circ_199712,RMVar_hsa_circ_199713,RMVar_hsa_circ_199711,RMVar_hsa_circ_199708,RMVar_hsa_circ_199709,RMVar_hsa_circ_378191,RMVar_hsa_circ_199707,RMVar_hsa_circ_199716,RMVar_hsa_circ_199717,RMVar_hsa_circ_305788,RMVar_hsa_circ_326917,RMVar_hsa_circ_361194,RMVar_hsa_circ_199718 53849 RMVar_ID_53849 Human_SNP_ID_838637893 A-to-I Human chr2 - 61527405 61527405 61527405 TAGCTCGGTGCAACCTTGATTTCCAGGGCTCAAGTGATCCTCCCATCTCGGTCTCCTGAGTAGTT TAGCTCGGTGCAACCTTGATTTCCAGGGCTCATGTGATCCTCCCATCTCGGTCTCCTGAGTAGTT T A XPO1 Ensembl:ENSG00000082898 Protein coding intron GSE100210 HepG2 cell line chr2:61527404..61527405 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_13933107 RMVar_hsa_circ_315608,RMVar_hsa_circ_200502,RMVar_hsa_circ_302279,RMVar_hsa_circ_200514,RMVar_hsa_circ_296615,RMVar_hsa_circ_200515,RMVar_hsa_circ_50486,RMVar_hsa_circ_200526,RMVar_hsa_circ_302621,RMVar_hsa_circ_316390,RMVar_hsa_circ_289683,RMVar_hsa_circ_200537,RMVar_hsa_circ_200543,RMVar_hsa_circ_308693,RMVar_hsa_circ_200559,RMVar_hsa_circ_346816,RMVar_hsa_circ_374780,RMVar_hsa_circ_294202,RMVar_hsa_circ_200560,RMVar_hsa_circ_333365,RMVar_hsa_circ_200568,RMVar_hsa_circ_304877,RMVar_hsa_circ_200569,RMVar_hsa_circ_200580,RMVar_hsa_circ_288660,RMVar_hsa_circ_289892,RMVar_hsa_circ_98453,RMVar_hsa_circ_200581,RMVar_hsa_circ_326823,RMVar_hsa_circ_301783,RMVar_hsa_circ_200588,RMVar_hsa_circ_284918,RMVar_hsa_circ_200590,RMVar_hsa_circ_278039,RMVar_hsa_circ_200594,RMVar_hsa_circ_200595,RMVar_hsa_circ_18859,RMVar_hsa_circ_200593,RMVar_hsa_circ_200600,RMVar_hsa_circ_297031 53850 RMVar_ID_53850 Human_SNP_ID_838660282 A-to-I Human chr2 - 64902275 64902275 64902275 GGGAGGCAGAGGTTGCGGTGAGCCGAGATTGCACCACTGCACTCCAGCCTGGGTAACAAGAGCGA GGGAGGCAGAGGTTGCGGTGAGCCGAGATTGCGCCACTGCACTCCAGCCTGGGTAACAAGAGCGA T C LINC02245 Ensembl:ENSG00000237638 lincRNA exon GSE38233 cultured B-cells chr2:64902274..64902275 24183664 RNA-Seq:(High) rs4671624 Functional Loss SNV ICGC 33..33 33 LAML 1 - GWAS_ID_5257,GWAS_ID_5258,GWAS_ID_5259,GWAS_ID_5260,GWAS_ID_5261,GWAS_ID_5262,GWAS_ID_5263,GWAS_ID_5264,GWAS_ID_5265,GWAS_ID_5266,GWAS_ID_5267 53851 RMVar_ID_53851 Human_SNP_ID_838693691 A-to-I Human chr2 - 96186654 96186654 96186654 TCAGTCCGTTATCACTCTGCTGTAGAAGGGGGACATGCCACATGTATTAGAAGGCATCTGCTGTA TCAGTCCGTTATCACTCTGCTGTAGAAGGGGGGCATGCCACATGTATTAGAAGGCATCTGCTGTA T C STARD7 Ensembl:ENSG00000084090 Protein coding 3'UTR GSE100210 HepG2 cell line chr2:96186653..96186654 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 3 lung Human_RBP_ID_557912,Human_RBP_ID_1197232,Human_RBP_ID_1591610,Human_RBP_ID_1925042,Human_RBP_ID_3636670,Human_RBP_ID_5194680,Human_RBP_ID_5502736,Human_RBP_ID_6958332,Human_RBP_ID_8850617,Human_RBP_ID_13986658,Human_RBP_ID_17277300,Human_RBP_ID_17392415,Human_RBP_ID_17509289,Human_RBP_ID_17699809,Human_RBP_ID_17963225,Human_RBP_ID_18767403,Human_RBP_ID_23889718,Human_RBP_ID_24377795,Human_RBP_ID_26488631,Human_RBP_ID_27016378,Human_RBP_ID_27699416 Human_miRNA_ID_2531683,Human_miRNA_ID_2911183,Human_miRNA_ID_2982774 RMVar_hsa_circ_201830,RMVar_hsa_circ_119875 53852 RMVar_ID_53852 Human_SNP_ID_838815463 A-to-I Human chr2 - 121586422 121586422 121586422 AAATTTTTCTTTCTTTTTAAAGAACAGGGGCTAGGTGCAGTGTCTCACTCCTGTAATCCCAGCAC AAATTTTTCTTTCTTTTTAAAGAACAGGGGCTTGGTGCAGTGTCTCACTCCTGTAATCCCAGCAC T A CLASP1 Ensembl:ENSG00000074054 Protein coding intron GSE100210 HepG2 cell line chr2:121586421..121586422 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_8,RMVar_hsa_circ_107706,RMVar_hsa_circ_202973,RMVar_hsa_circ_128046,RMVar_hsa_circ_202979,RMVar_hsa_circ_117254,RMVar_hsa_circ_202982,RMVar_hsa_circ_83520,RMVar_hsa_circ_202985,RMVar_hsa_circ_121076,RMVar_hsa_circ_202987,RMVar_hsa_circ_113253,RMVar_hsa_circ_202997,RMVar_hsa_circ_84402,RMVar_hsa_circ_203002,RMVar_hsa_circ_373344,RMVar_hsa_circ_203007,RMVar_hsa_circ_302647,RMVar_hsa_circ_120025,RMVar_hsa_circ_203014,RMVar_hsa_circ_203015,RMVar_hsa_circ_359257,RMVar_hsa_circ_68211,RMVar_hsa_circ_98014,RMVar_hsa_circ_203019 53853 RMVar_ID_53853 Human_SNP_ID_838912570 A-to-I Human chr2 - 75651421 75651421 75651421 AATCATTGCAATGATGAGTCCAGAGGACAGCTAGGTCTCCAAGTGGCAGCGAGTCAGTAACTTTA AATCATTGCAATGATGAGTCCAGAGGACAGCTGGGTCTCCAAGTGGCAGCGAGTCAGTAACTTTA T C SUPT4H1P1 Ensembl:ENSG00000226247 Pseudogene exon GSE100210 HepG2 cell line chr2:75651420..75651421 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 8 haematopoietic and lymphoid tissue Human_miRNA_ID_1862333,Human_miRNA_ID_1873355,Human_miRNA_ID_1909118 53854 RMVar_ID_53854 Human_SNP_ID_838916647 A-to-I Human chr2 - 201395382 201395382 201395382 CTGAAGAATTGTCAGGGAAGAGTGATGAGCTGATTCGATACCAAGAAGAGCTTTCCTCTCTTTTG CTGAAGAATTGTCAGGGAAGAGTGATGAGCTGGTTCGATACCAAGAAGAGCTTTCCTCTCTTTTG T C TRAK2 Ensembl:ENSG00000115993 Protein coding CDS GSE100210 HepG2 cell line chr2:201395381..201395382 29129909 RNA-Seq:(High) rs17857239 Functional Loss SNV COSMIC 33..33 33 pharynx nasopharyngeal_carcinoma 2 head and neck Human_RBP_ID_1582233,Human_RBP_ID_1907537,Human_RBP_ID_18752673,Human_RBP_ID_19002819 Human_Splice_Rec_345926,Human_Splice_Rec_345927,Human_Splice_Rec_345956 RMVar_hsa_circ_4751,RMVar_hsa_circ_17914,RMVar_hsa_circ_94151,RMVar_hsa_circ_115027,RMVar_hsa_circ_124257,RMVar_hsa_circ_110821,RMVar_hsa_circ_205894,RMVar_hsa_circ_205895,RMVar_hsa_circ_205896,RMVar_hsa_circ_205897,RMVar_hsa_circ_205898,RMVar_hsa_circ_205901,RMVar_hsa_circ_60909,RMVar_hsa_circ_19003,RMVar_hsa_circ_347894,RMVar_hsa_circ_6282,RMVar_hsa_circ_41999,RMVar_hsa_circ_1769,RMVar_hsa_circ_205903 53855 RMVar_ID_53855 Human_SNP_ID_838966275 A-to-I Human chr2 - 215943693 215943693 215943693 GGAACTACAGGCGCGTGCCACCACACCTGGCTAATTTTTTGTATTTTTAGTAGAGACGGGGTTTC GGAACTACAGGCGCGTGCCACCACACCTGGCTTATTTTTTGTATTTTTAGTAGAGACGGGGTTTC T A MREG Ensembl:ENSG00000118242 Protein coding 3'UTR GSE38233 cultured B-cells chr2:215943692..215943693 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 2 ovary RMVar_hsa_circ_93943,RMVar_hsa_circ_206796 53856 RMVar_ID_53856 Human_SNP_ID_839015390 A-to-I Human chr2 - 113599773 113599773 113599773 CATTAGTGCCCGTTGGAGAAAACGGGAATCCCAAAGAAATGGTGGGTCCTGGCCATCCGTGAGAT CATTAGTGCCCGTTGGAGAAAACGGGAATCCCGAAGAAATGGTGGGTCCTGGCCATCCGTGAGAT T C DDX11L2 Ensembl:ENSG00000236397 Pseudogene exon GSE100210 HepG2 cell line chr2:113599772..113599773 29129909 RNA-Seq:(High) rs67465876 Functional Loss SNV ICGC 33..33 33 ESCA 1 - 53857 RMVar_ID_53857 Human_SNP_ID_839181262 A-to-I Human chr2 - 206134938 206134938 206134938 AGGTCTCACTATGTTGCCCAGGCTGCAGTGCAATGGCAGAATTGTAGCTGACTGTAGCCTCAAAC AGGTCTCACTATGTTGCCCAGGCTGCAGTGCAGTGGCAGAATTGTAGCTGACTGTAGCCTCAAAC T C NDUFS1 Ensembl:ENSG00000023228 Protein coding intron GSE38233 cultured B-cells chr2:206134937..206134938 24183664 RNA-Seq:(High) rs12464101 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_17570985 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_70745,RMVar_hsa_circ_325297,RMVar_hsa_circ_342117,RMVar_hsa_circ_378796,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_206316 53858 RMVar_ID_53858 Human_SNP_ID_839185984 A-to-I Human chr2 - 127851485 127851485 127851485 GTGATCCTCCTGCCTTGGCCTCCCAAAGTGCTAGGATTACAGGCATGAGCTGCTAAGCCTGGCCT GTGATCCTCCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCTGCTAAGCCTGGCCT T C POLR2D Ensembl:ENSG00000144231 Protein coding intron GSE100210 HepG2 cell line chr2:127851484..127851485 29129909 RNA-Seq:(High) rs1182993480 Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_203112,RMVar_hsa_circ_317749 53859 RMVar_ID_53859 Human_SNP_ID_839338597 A-to-I Human chr2 - 97206074 97206074 97206074 TCTCTGGCTATACTCAAAACAGAATCTTCCTCATCACTTGTAGCCTGAATGGAATTTGAAACAAA TCTCTGGCTATACTCAAAACAGAATCTTCCTCGTCACTTGTAGCCTGAATGGAATTTGAAACAAA T C - - Other Unknown GSE107867 ASD brains,cerebellum chr2:97206073..97206074 30559470 RNA-Seq:(High) rs771135449 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 8 liver 53860 RMVar_ID_53860 Human_SNP_ID_839389020 A-to-I Human chr2 - 76998559 76998559 76998559 TTAAATGTGCAGATTCCTGGGTCTCATCCTGAAGTTTTTGACTTCATAGTTGGTTGTTGACATTA TTAAATGTGCAGATTCCTGGGTCTCATCCTGACGTTTTTGACTTCATAGTTGGTTGTTGACATTA T G LRRTM4 Ensembl:ENSG00000176204 Protein coding intron GSE107867 ASD brains,frontal_cortex chr2:76998558..76998559 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 4 oesophagus RMVar_hsa_circ_201425 53861 RMVar_ID_53861 Human_SNP_ID_839403620 A-to-I Human chr2 - 85319404 85319404 85319404 TGGGAGGCCGAGGCGGGGGGATCACGAGGTCAAGAGATCGAGACCATCCTGGCCAACATGGTGAA TGGGAGGCCGAGGCGGGGGGATCACGAGGTCACGAGATCGAGACCATCCTGGCCAACATGGTGAA T G TGOLN2 Ensembl:ENSG00000152291 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells chr2:85319403..85319404 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_miRNA_ID_1689857 53862 RMVar_ID_53862 Human_SNP_ID_839428622 A-to-I Human chr2 + 9936318 9936318 9936318 CTGACCTCGTGATCCACCCGCCTTGGCCTCCTAAAGTGCTGGGATTACAGGCGTGAGCCACCGTG CTGACCTCGTGATCCACCCGCCTTGGCCTCCTGAAGTGCTGGGATTACAGGCGTGAGCCACCGTG A G - - Other Unknown GSE100210 HepG2 cell line chr2:9936318..9936319 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 CLLE 1 - 53863 RMVar_ID_53863 Human_SNP_ID_839592338 A-to-I Human chr2 + 203303118 203303118 203303118 TGCCTCCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCTGAGACTACGGGTATGTG TGCCTCCCAGGTTCAAGCAATTCTCCTGCCTCGGCCTCCTGAGTAGCTGAGACTACGGGTATGTG A G CYP20A1 Ensembl:ENSG00000119004 Protein coding intron GSE38233 cultured B-cells chr2:203303117..203303118 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 53864 RMVar_ID_53864 Human_SNP_ID_839600976 A-to-I Human chr2 - 55662588 55662588 55662588 CTCACTGCAACCTCGCCTGTTGGATTCGAGCTATTCTTCTGCCTCAGCCTCCCAAGCAGCTGGGA CTCACTGCAACCTCGCCTGTTGGATTCGAGCTGTTCTTCTGCCTCAGCCTCCCAAGCAGCTGGGA T C PNPT1 Ensembl:ENSG00000138035 Protein coding intron GSE38233 cultured B-cells chr2:55662587..55662588 24183664 RNA-Seq:(High) rs577448925 Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_25551409 RMVar_hsa_circ_1092,RMVar_hsa_circ_95213,RMVar_hsa_circ_113405,RMVar_hsa_circ_120288,RMVar_hsa_circ_200079,RMVar_hsa_circ_200080,RMVar_hsa_circ_200083,RMVar_hsa_circ_362348,RMVar_hsa_circ_367895,RMVar_hsa_circ_119178,RMVar_hsa_circ_200089,RMVar_hsa_circ_109983,RMVar_hsa_circ_31717,RMVar_hsa_circ_200092,RMVar_hsa_circ_200093,RMVar_hsa_circ_57208,RMVar_hsa_circ_91094,RMVar_hsa_circ_200094,RMVar_hsa_circ_329548,RMVar_hsa_circ_357916,RMVar_hsa_circ_200104,RMVar_hsa_circ_64638,RMVar_hsa_circ_200099,RMVar_hsa_circ_266803,RMVar_hsa_circ_124374,RMVar_hsa_circ_200102,RMVar_hsa_circ_99184,RMVar_hsa_circ_324216,RMVar_hsa_circ_329333,RMVar_hsa_circ_311056,RMVar_hsa_circ_323444,RMVar_hsa_circ_288697,RMVar_hsa_circ_39697,RMVar_hsa_circ_29288,RMVar_hsa_circ_377349,RMVar_hsa_circ_341692,RMVar_hsa_circ_64870,RMVar_hsa_circ_6794,RMVar_hsa_circ_36565,RMVar_hsa_circ_355086,RMVar_hsa_circ_14021,RMVar_hsa_circ_9112,RMVar_hsa_circ_200105,RMVar_hsa_circ_37316,RMVar_hsa_circ_50100,RMVar_hsa_circ_344819,RMVar_hsa_circ_371182,RMVar_hsa_circ_301581,RMVar_hsa_circ_47920,RMVar_hsa_circ_308967,RMVar_hsa_circ_341419,RMVar_hsa_circ_355724,RMVar_hsa_circ_364807,RMVar_hsa_circ_314778,RMVar_hsa_circ_300426,RMVar_hsa_circ_200106,RMVar_hsa_circ_200107,RMVar_hsa_circ_200108 53865 RMVar_ID_53865 Human_SNP_ID_839620446 A-to-I Human chr2 + 135510728 135510728 135510728 AGCTCGAGTCTTCTTCTCTTCCACATTCAGACAGACCTCACCTCTGAACATGATGGGCCTGTTGC AGCTCGAGTCTTCTTCTCTTCCACATTCAGACGGACCTCACCTCTGAACATGATGGGCCTGTTGC A G - - Other Unknown GSE100210 HepG2 cell line chr2:135510727..135510728 29129909 RNA-Seq:(High) rs1237162912 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 8 haematopoietic and lymphoid tissue 53866 RMVar_ID_53866 Human_SNP_ID_839733247 A-to-I Human chr2 - 177235717 177235717 177235717 GCTCAAGCAATCCTCTCACTTCAGTCTCCCTAATAGTTGGGACTACAGGCTCGTATCACCACGTG GCTCAAGCAATCCTCTCACTTCAGTCTCCCTACTAGTTGGGACTACAGGCTCGTATCACCACGTG T G NFE2L2 Ensembl:ENSG00000116044 Protein coding intron GSE47997 K562 cells&HepG2 cells chr2:177235716..177235717 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_107949,RMVar_hsa_circ_204828 53867 RMVar_ID_53867 Human_SNP_ID_839766881 A-to-I Human chr2 + 241111335 241111335 241111335 GATATGGGCGGTGCAGCAGAGCACTGCAGCAGAGGGCCAGGAGGGTCCAAGCAGTGCTGTGATCA GATATGGGCGGTGCAGCAGAGCACTGCAGCAGGGGGCCAGGAGGGTCCAAGCAGTGCTGTGATCA A G - - Other Unknown GSE100210 HepG2 cell line chr2:241111334..241111335 29129909 RNA-Seq:(High) rs2310874 Functional Loss SNV ICGC 33..33 33 LAML 1 - 53868 RMVar_ID_53868 Human_SNP_ID_839783950 A-to-I Human chr2 - 97204202 97204202 97204202 CCTCTGGCTATATTCAAAACAGAATCTTTCTCATCACTTGTAGCCTGAATGGAATTTGAAATGAA CCTCTGGCTATATTCAAAACAGAATCTTTCTCGTCACTTGTAGCCTGAATGGAATTTGAAATGAA T C - - Other Unknown GSE107867 ASD brains,frontal_cortex;ASD brains,temporal_cortex chr2:97204201..97204202 30559470 RNA-Seq:(High) rs553334409 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 KICH,kidney chromophobe_renal_cell_carcinoma 5 kidney 53869 RMVar_ID_53869 Human_SNP_ID_839815067 A-to-I Human chr2 - 241262725 241262725 241262725 CTGTCATGAAAGCTCGGAAGGACATTGTTGCTAGACTGCAGACTCAGGTGGGTAGCCTGAGGCCT CTGTCATGAAAGCTCGGAAGGACATTGTTGCTGGACTGCAGACTCAGGTGGGTAGCCTGAGGCCT T C HDLBP Ensembl:ENSG00000115677 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector chr2:241262724..241262725 29967493 RNA-Seq:(High) rs1473316822 Functional Loss SNV TCGA 33..33 33 BRCA 1 - Human_RBP_ID_916100,Human_RBP_ID_1584938,Human_RBP_ID_1913738,Human_RBP_ID_3620125,Human_RBP_ID_3959982,Human_RBP_ID_5194547,Human_RBP_ID_5589221,Human_RBP_ID_8515605,Human_RBP_ID_8847033,Human_RBP_ID_9104664,Human_RBP_ID_9385906,Human_RBP_ID_13821461,Human_RBP_ID_18757251,Human_RBP_ID_19001021,Human_RBP_ID_22076918,Human_RBP_ID_24546275,Human_RBP_ID_26338899 Human_Splice_Rec_381265,Human_Splice_Rec_381319,Human_Splice_Rec_381375,Human_Splice_Rec_381427,Human_Splice_Rec_381499,Human_Splice_Rec_381627,Human_Splice_Rec_381653,Human_Splice_Rec_381669,Human_Splice_Rec_381693 Human_miRNA_ID_2946864,Human_miRNA_ID_2946865 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_14643,RMVar_hsa_circ_6493,RMVar_hsa_circ_113630,RMVar_hsa_circ_208072,RMVar_hsa_circ_89716,RMVar_hsa_circ_208078,RMVar_hsa_circ_353105,RMVar_hsa_circ_26458,RMVar_hsa_circ_19903,RMVar_hsa_circ_20061,RMVar_hsa_circ_208086,RMVar_hsa_circ_324760,RMVar_hsa_circ_359290,RMVar_hsa_circ_48205,RMVar_hsa_circ_62964,RMVar_hsa_circ_371246,RMVar_hsa_circ_208090,RMVar_hsa_circ_354695,RMVar_hsa_circ_59639,RMVar_hsa_circ_309108,RMVar_hsa_circ_359828,RMVar_hsa_circ_208091,RMVar_hsa_circ_92340,RMVar_hsa_circ_15630,RMVar_hsa_circ_208094,RMVar_hsa_circ_208096,RMVar_hsa_circ_102687,RMVar_hsa_circ_50433,RMVar_hsa_circ_304573,RMVar_hsa_circ_208097 53870 RMVar_ID_53870 Human_SNP_ID_839842402 A-to-I Human chr2 - 223756095 223756095 223756095 ACCTCAGGTGATCCGCCCGCCTTGGCCTTCCAAAGTGCTGGAATTACAGGCATGAGCCGCTGCAC ACCTCAGGTGATCCGCCCGCCTTGGCCTTCCAGAGTGCTGGAATTACAGGCATGAGCCGCTGCAC T C AP1S3 Ensembl:ENSG00000152056 Protein coding intron GSE99789;GSE123020:GSM3490829,GSM3490830,GSM3490831 esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109 cell line chr2:223756094..223756095 29796672,32596459 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 53871 RMVar_ID_53871 Human_SNP_ID_839860189 A-to-I Human chr2 + 27067657 27067657 27067657 CCTGATTCATTCAACATACCAGGTCTGTACCCACTGCCACTGAAATCTGGGTTTGCCAGCCTCCT CCTGATTCATTCAACATACCAGGTCTGTACCCGCTGCCACTGAAATCTGGGTTTGCCAGCCTCCT A G AGBL5 Ensembl:ENSG00000084693 Protein coding intron GSE38233 cultured B-cells chr2:27067656..27067657 24183664 RNA-Seq:(High) rs11681145 Functional Loss SNV ICGC 33..33 33 COCA 6 - GWAS_ID_3514,GWAS_ID_3515,GWAS_ID_3516,GWAS_ID_3517,GWAS_ID_3518,GWAS_ID_3519,GWAS_ID_3520 RMVar_hsa_circ_84980,RMVar_hsa_circ_197868 53872 RMVar_ID_53872 Human_SNP_ID_839860464 A-to-I Human chr2 - 38602832 38602832 38602832 TTGGCTCGGTAATTGAGAGGAGCGGCCGCTCCAGAGCTTCCTCCCGGGGCGCCCCCCTCAGTCCG TTGGCTCGGTAATTGAGAGGAGCGGCCGCTCCCGAGCTTCCTCCCGGGGCGCCCCCCTCAGTCCG T G HNRNPLL Ensembl:ENSG00000143889 Protein coding 5'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr2:38602831..38602832 30559470 RNA-Seq:(High) rs556524230 Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_777832,Human_RBP_ID_1067898,Human_RBP_ID_4624226,Human_RBP_ID_9297132,Human_RBP_ID_9330422,Human_RBP_ID_18421743,Human_RBP_ID_26338520 53873 RMVar_ID_53873 Human_SNP_ID_839889753 A-to-I Human chr2 + 128194336 128194336 128194336 CAGGCTGGAGTGGAGTGCAGTGGCACAATCTCAGCTCACTGCAGCCTCTGCCTCCCGGGTTCAAG CAGGCTGGAGTGGAGTGCAGTGGCACAATCTCGGCTCACTGCAGCCTCTGCCTCCCGGGTTCAAG A G UGGT1 Ensembl:ENSG00000136731 Protein coding 3'UTR GSE38233;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line chr2:128194335..128194336 24183664,29796672,31158229,31158229 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_13608460 RMVar_hsa_circ_83982,RMVar_hsa_circ_203205 53874 RMVar_ID_53874 Human_SNP_ID_839900166 A-to-I Human chr2 - 68133637 68133629 68133638 GGGGTTCTCCTGCCTCAGCCTCCCGAGTAACTAGGATTACAGGTGCCCGCCACGACGCCTGGCTA GGGGTTCTCCTGCCTCAGCCTCCCGAGTAAC_________AGGTGCCCGCCACGACGCCTGGCTA TGTAATCCTA T AC017083.3,WDR92 Ensembl:ENSG00000273398,Ensembl:ENSG00000243667 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line chr2:68133636..68133637 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 32..40 33 LICA 1 - RMVar_hsa_circ_9785,RMVar_hsa_circ_278880,RMVar_hsa_circ_283619,RMVar_hsa_circ_346441,RMVar_hsa_circ_277015,RMVar_hsa_circ_200824,RMVar_hsa_circ_200826,RMVar_hsa_circ_200827,RMVar_hsa_circ_200825 53875 RMVar_ID_53875 Human_SNP_ID_839951164 A-to-I Human chr2 - 58461589 58461589 58461589 CAGCTAACTACAGGGCTGTTGGCCCCACTACTAAGGCGGACAAATCAGCTGCAGAGAAGAGAAGA CAGCTAACTACAGGGCTGTTGGCCCCACTACTGAGGCGGACAAATCAGCTGCAGAGAAGAGAAGA T C AC007238.1 Ensembl:ENSG00000231043 Pseudogene exon GSE100210 HepG2 cell line chr2:58461588..58461589 29129909 RNA-Seq:(High) rs878879180 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_miRNA_ID_1823556 53876 RMVar_ID_53876 Human_SNP_ID_839979908 A-to-I Human chr2 + 37239539 37239539 37239539 GATATACCCTAGAGAAACTAGTGTATATGTGTACCAGGAGACACATACAAGAAGATAGCAGCATT GATATACCCTAGAGAAACTAGTGTATATGTGTGCCAGGAGACACATACAAGAAGATAGCAGCATT A G NDUFAF7 Ensembl:ENSG00000003509 Protein coding intron GSE38233 cultured B-cells chr2:37239538..37239539 24183664 RNA-Seq:(High) rs11124569 Functional Loss SNV ICGC 33..33 33 LAML 2 - GWAS_ID_1630,GWAS_ID_1631,GWAS_ID_1632,GWAS_ID_1633,GWAS_ID_1634,GWAS_ID_1635,GWAS_ID_1636,GWAS_ID_1637,GWAS_ID_1638,GWAS_ID_1639,GWAS_ID_1640,GWAS_ID_1641,GWAS_ID_1642,GWAS_ID_1643,GWAS_ID_1644,GWAS_ID_1645,GWAS_ID_1646,GWAS_ID_1647,GWAS_ID_1648,GWAS_ID_1649,GWAS_ID_1650,GWAS_ID_1651,GWAS_ID_1652,GWAS_ID_1653,GWAS_ID_1654,GWAS_ID_1655,GWAS_ID_1656,GWAS_ID_1657,GWAS_ID_1658,GWAS_ID_1659 RMVar_hsa_circ_107491,RMVar_hsa_circ_301687,RMVar_hsa_circ_198967,RMVar_hsa_circ_198968,RMVar_hsa_circ_198969,RMVar_hsa_circ_286444 53877 RMVar_ID_53877 Human_SNP_ID_839998232 A-to-I Human chr2 + 156442724 156442724 156442724 AGGAGGCTGAGGTGGGAGGATCCTTTGAGCCTAGGAGGCCGAGGCTGCAGTGAGCCATGATTGCA AGGAGGCTGAGGTGGGAGGATCCTTTGAGCCTGGGAGGCCGAGGCTGCAGTGAGCCATGATTGCA A G GPD2 Ensembl:ENSG00000115159 Protein coding intron GSE100210 HepG2 cell line chr2:156442723..156442724 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 53878 RMVar_ID_53878 Human_SNP_ID_840044714 A-to-I Human chr2 - 61187626 61187626 61187626 CAAGAAATTTGATTCTGTAAAGAATCCTCTTTAGCTGTGGCCTGGCAGTATATAAATGGTGCTTT CAAGAAATTTGATTCTGTAAAGAATCCTCTTTCGCTGTGGCCTGGCAGTATATAAATGGTGCTTT T G USP34 Ensembl:ENSG00000115464 Protein coding 3'UTR GSE100210 HepG2 cell line chr2:61187625..61187626 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_553013,Human_RBP_ID_5118491,Human_RBP_ID_18167166 RMVar_hsa_circ_121659,RMVar_hsa_circ_200273 53879 RMVar_ID_53879 Human_SNP_ID_840055881 A-to-I Human chr2 + 38781151 38781151 38781151 CACCACACCCAGCTAATATTTGTATTTTTAGTAGGGATTGGGTTTCACCATCTTGGCCAGAGGTT CACCACACCCAGCTAATATTTGTATTTTTAGTGGGGATTGGGTTTCACCATCTTGGCCAGAGGTT A G GEMIN6 Ensembl:ENSG00000152147 Protein coding intron GSE100210 HepG2 cell line chr2:38781150..38781151 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_199046,RMVar_hsa_circ_101692 53880 RMVar_ID_53880 Human_SNP_ID_840107023 A-to-I Human chr2 - 58252099 58252099 58252099 GTCCTCCCAGGGACACCCATTAAAGTGCTGACATAGGCTTTGATGCTCATGCGGCCGTTCTGGAG GTCCTCCCAGGGACACCCATTAAAGTGCTGACGTAGGCTTTGATGCTCATGCGGCCGTTCTGGAG T C lnc-FANCL-4 RNACentral:URS00008B7619 lincRNA intron GSE100210 HepG2 cell line chr2:58252098..58252099 29129909 RNA-Seq:(High) rs878880258 Functional Loss SNV ICGC 33..33 33 LAML 2 - 53881 RMVar_ID_53881 Human_SNP_ID_840111225 A-to-I Human chr2 - 141708939 141708939 141708939 GGTACCAAGCAACAGAAATTTATTCTCTCACAAGTCTAGGGGCTGGAAGTCCAAGATCAAGGTAT GGTACCAAGCAACAGAAATTTATTCTCTCACACGTCTAGGGGCTGGAAGTCCAAGATCAAGGTAT T G LRP1B Ensembl:ENSG00000168702 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,cerebellum chr2:141708938..141708939 29129909,30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_121478,RMVar_hsa_circ_203553,RMVar_hsa_circ_118491,RMVar_hsa_circ_203571,RMVar_hsa_circ_82511,RMVar_hsa_circ_203606,RMVar_hsa_circ_18654,RMVar_hsa_circ_77134,RMVar_hsa_circ_203611,RMVar_hsa_circ_203616,RMVar_hsa_circ_81775,RMVar_hsa_circ_377585,RMVar_hsa_circ_203629 53882 RMVar_ID_53882 Human_SNP_ID_840111238 A-to-I Human chr2 - 141708939 141708939 141708939 GGTACCAAGCAACAGAAATTTATTCTCTCACAAGTCTAGGGGCTGGAAGTCCAAGATCAAGGTAT GGTACCAAGCAACAGAAATTTATTCTCTCACAGGTCTAGGGGCTGGAAGTCCAAGATCAAGGTAT T C LRP1B Ensembl:ENSG00000168702 Protein coding intron GSE100210;GSE107867 HepG2 cell line;ASD brains,cerebellum chr2:141708938..141708939 29129909,30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_121478,RMVar_hsa_circ_203553,RMVar_hsa_circ_118491,RMVar_hsa_circ_203571,RMVar_hsa_circ_82511,RMVar_hsa_circ_203606,RMVar_hsa_circ_18654,RMVar_hsa_circ_77134,RMVar_hsa_circ_203611,RMVar_hsa_circ_203616,RMVar_hsa_circ_81775,RMVar_hsa_circ_377585,RMVar_hsa_circ_203629 53883 RMVar_ID_53883 Human_SNP_ID_840121365 A-to-I Human chr2 - 65092151 65092151 65092151 ATTCTGCCTCAGCCTCTCGAGTAGCTGGGACCACAGGCGCACGCCAGCATACTTGGCTAATTTTT ATTCTGCCTCAGCCTCTCGAGTAGCTGGGACCTCAGGCGCACGCCAGCATACTTGGCTAATTTTT T A RAB1A Ensembl:ENSG00000138069 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr2:65092150..65092151 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_200775,RMVar_hsa_circ_200774,RMVar_hsa_circ_361917,RMVar_hsa_circ_20271,RMVar_hsa_circ_200776,RMVar_hsa_circ_275997,RMVar_hsa_circ_278716,RMVar_hsa_circ_200777 53884 RMVar_ID_53884 Human_SNP_ID_840130486 A-to-I Human chr2 + 112338895 112338853 112338895 ATATATATATATATATATATATATATATATATATATATATATATATATATAATTTTTTTTTTTTG _________________________________TATATATATATATATATAATTTTTTTTTTTTG GTGTATATATATATATATATATATATATATATATATATATATA G ZC3H6 Ensembl:ENSG00000188177 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells chr2:112338894..112338895 23474544 RNA-Seq:(High) rs778683215 Functional Loss DEL ICGC 1..33 33 ESCA 1 - RMVar_hsa_circ_118236,RMVar_hsa_circ_269195,RMVar_hsa_circ_202633 53885 RMVar_ID_53885 Human_SNP_ID_840477675 A-to-I Human chr2 + 230165695 230165695 230165695 ATAAACGCATTGCCTTAAGTATGTGACACATTACAGATATTTTATTTTTGACTTTGACATTAAAA ATAAACGCATTGCCTTAAGTATGTGACACATTGCAGATATTTTATTTTTGACTTTGACATTAAAA A G AC009950.1 Ensembl:ENSG00000225963 lincRNA intron GSE38233 cultured B-cells chr2:230165694..230165695 24183664 RNA-Seq:(High) rs1060759 Functional Loss SNV ICGC 33..33 33 LAML 1 - GWAS_ID_4690,GWAS_ID_4691,GWAS_ID_4692,GWAS_ID_4693,GWAS_ID_4694,GWAS_ID_4695,GWAS_ID_4696,GWAS_ID_4697,GWAS_ID_4698,GWAS_ID_4699,GWAS_ID_4700,GWAS_ID_4701,GWAS_ID_4702,GWAS_ID_4703,GWAS_ID_4704 53886 RMVar_ID_53886 Human_SNP_ID_840485780 A-to-I Human chr2 + 24002143 24002143 24002143 TAAAAATTACAAAAATTAGTGCAGTAGCTCACACCTGTAATCCCAGCACTTTGGGACACTAAAGC TAAAAATTACAAAAATTAGTGCAGTAGCTCACGCCTGTAATCCCAGCACTTTGGGACACTAAAGC A G UBXN2A Ensembl:ENSG00000173960 Protein coding 3'UTR GSE38233 cultured B-cells chr2:24002142..24002143 24183664 RNA-Seq:(High) rs1473130025 Functional Loss SNV ICGC 33..33 33 PBCA 1 - 53887 RMVar_ID_53887 Human_SNP_ID_840512741 A-to-I Human chr2 + 10156694 10156694 10156694 GGACAGGGTCTCTGTCACCTAGGCTGGAGTGCAGTGGTGCAACCTCAGCTCCCTGTAACTTCCGC GGACAGGGTCTCTGTCACCTAGGCTGGAGTGCGGTGGTGCAACCTCAGCTCCCTGTAACTTCCGC A G RRM2 Ensembl:ENSG00000171848 Protein coding intron GSE100210 HepG2 cell line chr2:10156693..10156694 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_13563396 53888 RMVar_ID_53888 Human_SNP_ID_840584122 A-to-I Human chr2 + 44602257 44602257 44602257 TCCTGAGCTCTAGCTCCCAAAGTGCTGGTATTAGAAGCATGAGCCACCATGCCTGGCCCTGCTTT TCCTGAGCTCTAGCTCCCAAAGTGCTGGTATTGGAAGCATGAGCCACCATGCCTGGCCCTGCTTT A G CAMKMT Ensembl:ENSG00000143919 Protein coding intron GSE100210 HepG2 cell line chr2:44602256..44602257 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_13900134 53889 RMVar_ID_53889 Human_SNP_ID_840650033 A-to-I Human chr2 + 112629566 112629566 112629566 AGCATTTTGGGAGGCCGAGGTGGCTGGATCACAAGGTCAGGAGTTCGAGACCAGTCTGGCCAACA AGCATTTTGGGAGGCCGAGGTGGCTGGATCACTAGGTCAGGAGTTCGAGACCAGTCTGGCCAACA A T - - Other Unknown GSE100210 HepG2 cell line chr2:112629566..112629567 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 53890 RMVar_ID_53890 Human_SNP_ID_840679818 A-to-I Human chr2 - 127843857 127843857 127843857 GCAGTCCACCTGTTTCCGCCTCCCAAATGCTGAGATTAGAGGCATGAGTCACTGCACCCAGCCCG GCAGTCCACCTGTTTCCGCCTCCCAAATGCTGGGATTAGAGGCATGAGTCACTGCACCCAGCCCG T C POLR2D Ensembl:ENSG00000144231 Protein coding 3'UTR GSE100210 HepG2 cell line chr2:127843856..127843857 29129909 RNA-Seq:(High) rs11539730 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 2 liver 53891 RMVar_ID_53891 Human_SNP_ID_840698836 A-to-I Human chr2 + 61050749 61050749 61050749 TCACGCCATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCGCCTGCCACCAGGCCCG TCACGCCATTCTCCTGCCTCAGCCTCCCGAGTGGCTGGGACTACAGGCGCCTGCCACCAGGCCCG A G PEX13 Ensembl:ENSG00000162928 Protein coding 3'UTR GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line chr2:61050748..61050749 31158229 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 53892 RMVar_ID_53892 Human_SNP_ID_840751305 A-to-I Human chr2 - 58461592 58461592 58461592 CCACAGCTAACTACAGGGCTGTTGGCCCCACTACTAAGGCGGACAAATCAGCTGCAGAGAAGAGA CCACAGCTAACTACAGGGCTGTTGGCCCCACTGCTAAGGCGGACAAATCAGCTGCAGAGAAGAGA T C AC007238.1 Ensembl:ENSG00000231043 Pseudogene exon GSE100210 HepG2 cell line chr2:58461591..58461592 29129909 RNA-Seq:(High) rs879198444 Functional Loss SNV ICGC 33..33 33 LAML 2 - 53893 RMVar_ID_53893 Human_SNP_ID_840775249 A-to-I Human chr2 - 170999923 170999923 170999923 GACCCTGTCTGTATAAATTTTTTAAAAAAATTAGCCAGGCATGGTGGTGTGTGCCTGTGGTCCCA GACCCTGTCTGTATAAATTTTTTAAAAAAATTTGCCAGGCATGGTGGTGTGTGCCTGTGGTCCCA T A TLK1 Ensembl:ENSG00000198586 Protein coding intron GSE38233 cultured B-cells chr2:170999922..170999923 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 5 liver Human_RBP_ID_17570036 RMVar_hsa_circ_111553,RMVar_hsa_circ_127504,RMVar_hsa_circ_367800,RMVar_hsa_circ_204579,RMVar_hsa_circ_204580 53894 RMVar_ID_53894 Human_SNP_ID_840835365 A-to-I Human chr2 + 113205366 113205366 113205366 GTTTTAAGAAGATGAGCTGGGCGCGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAA GTTTTAAGAAGATGAGCTGGGCGCGGTGGCTCGTGCCTGTAATCCCAGCACTTTGGGAGGCTGAA A G PSD4 Ensembl:ENSG00000125637 Protein coding 3'UTR GSE38233 cultured B-cells chr2:113205365..113205366 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 2 pancreas 53895 RMVar_ID_53895 Human_SNP_ID_840897207 A-to-I Human chr2 + 230166660 230166660 230166660 CTTAGTTTGTTTTTCATAGTGATCTGAGTGTTAAAATTCTGTTAACTTTTATTGTTGTACCTGGG CTTAGTTTGTTTTTCATAGTGATCTGAGTGTTGAAATTCTGTTAACTTTTATTGTTGTACCTGGG A G AC009950.1 Ensembl:ENSG00000225963 lincRNA intron GSE38233 cultured B-cells chr2:230166659..230166660 24183664 RNA-Seq:(High) rs13026121 Functional Loss SNV ICGC 33..33 33 LAML 1 - GWAS_ID_4705,GWAS_ID_4706,GWAS_ID_4707,GWAS_ID_4708,GWAS_ID_4709,GWAS_ID_4710,GWAS_ID_4711,GWAS_ID_4712,GWAS_ID_4713,GWAS_ID_4714,GWAS_ID_4715,GWAS_ID_4716,GWAS_ID_4717,GWAS_ID_4718,GWAS_ID_4719,GWAS_ID_4720,GWAS_ID_4721,GWAS_ID_4722,GWAS_ID_4723 53896 RMVar_ID_53896 Human_SNP_ID_840926247 A-to-I Human chr2 - 223753384 223753384 223753384 AACATTTTTTTAAAAATTAAAAAATAGAGATGAGCTCTCACTGTGTTGCCCAGGCTGGTCTTGAA AACATTTTTTTAAAAATTAAAAAATAGAGATGCGCTCTCACTGTGTTGCCCAGGCTGGTCTTGAA T G AP1S3 Ensembl:ENSG00000152056 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line chr2:223753383..223753384 29129909,31158229,31158229,31158229 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 2 prostate 53897 RMVar_ID_53897 Human_SNP_ID_840960190 A-to-I Human chr2 + 201286639 201286639 201286639 GTTTGTTTTGTTTTGTTTTGTTTTTTTGAGACAGAATCTCGCTCTGTCGCCCAGGCTGGAGTGCA GTTTGTTTTGTTTTGTTTTGTTTTTTTGAGACGGAATCTCGCTCTGTCGCCCAGGCTGGAGTGCA A G CASP8 Ensembl:ENSG00000064012 Protein coding 3'UTR GSE38233;GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line chr2:201286638..201286639 24183664,29129909,32596459,32596459 RNA-Seq:(High) rs1472140233 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 10 haematopoietic and lymphoid tissue 53898 RMVar_ID_53898 Human_SNP_ID_841007279 A-to-I Human chr2 + 241111333 241111333 241111333 CAGATATGGGCGGTGCAGCAGAGCACTGCAGCAGAGGGCCAGGAGGGTCCAAGCAGTGCTGTGAT CAGATATGGGCGGTGCAGCAGAGCACTGCAGCGGAGGGCCAGGAGGGTCCAAGCAGTGCTGTGAT A G - - Other Unknown GSE100210 HepG2 cell line chr2:241111332..241111333 29129909 RNA-Seq:(High) rs2310875 Functional Loss SNV ICGC 33..33 33 LAML 1 - 53899 RMVar_ID_53899 Human_SNP_ID_841009677 A-to-I Human chr2 + 131513717 131513717 131513717 AAAAATAGCCAGCCACGATGGCTCATGCTTGTAATCCCAGCACTTTGGGAGGTTGAGGCAGGCGG AAAAATAGCCAGCCACGATGGCTCATGCTTGTGATCCCAGCACTTTGGGAGGTTGAGGCAGGCGG A G SMPD4BP Ensembl:ENSG00000152117 Pseudogene intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr2:131513717..131513718 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_35467 53900 RMVar_ID_53900 Human_SNP_ID_841065047 A-to-I Human chr2 + 24002509 24002508 24002509 CTTGGCTCACTGCAACTTGTCCCCCCGGGTTCAAGCGATTCTTCTGCCACAGCCTCCCGAGTAGC CTTGGCTCACTGCAACTTGTCCCCCCGGGTTC_AGCGATTCTTCTGCCACAGCCTCCCGAGTAGC CA C UBXN2A Ensembl:ENSG00000173960 Protein coding 3'UTR GSE100210 HepG2 cell line chr2:24002508..24002509 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 33..33 33 PRAD 1 - 53901 RMVar_ID_53901 Human_SNP_ID_841111024 A-to-I Human chr2 - 174564401 174564401 174564401 TCACCCAGGCTGGTCTTGAGCTTCTGGCCTCAAGTAGTCCCCTGCCTTAACCTCCCAAAGCACTG TCACCCAGGCTGGTCTTGAGCTTCTGGCCTCACGTAGTCCCCTGCCTTAACCTCCCAAAGCACTG T G WIPF1 Ensembl:ENSG00000115935 Protein coding intron GSE100210 HepG2 cell line chr2:174564400..174564401 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_123832,RMVar_hsa_circ_204758,RMVar_hsa_circ_106689,RMVar_hsa_circ_204757 53902 RMVar_ID_53902 Human_SNP_ID_841124969 A-to-I Human chr2 - 164950197 164950197 164950197 AACTCTGTTGCCAGTAACTTCAGACCTTGGCTAAGCCGTTTTAACCTACTGAAGTCCAAATTTTC AACTCTGTTGCCAGTAACTTCAGACCTTGGCTGAGCCGTTTTAACCTACTGAAGTCCAAATTTTC T C SLC38A11 Ensembl:ENSG00000169507 Protein coding intron GSE107867 ASD brains,temporal_cortex chr2:164950196..164950197 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - RMVar_hsa_circ_22184,RMVar_hsa_circ_53481,RMVar_hsa_circ_55499 53903 RMVar_ID_53903 Human_SNP_ID_856758261 A-to-I Human chr5 - 159203632 159203630 159203633 AATTTTAGGTCTTCTCCAAGAAAAAAAAAAAGAAAAAAAAAAACAACATGGCTGCAAAGGAGAAA AATTTTAGGTCTTCTCCAAGAAAAAAAAAAA___AAAAAAAAACAACATGGCTGCAAAGGAGAAA TTTC T RNF145 Ensembl:ENSG00000145860 Protein coding CDS GSE38233 cultured B-cells chr5:159203632..159203633 24183664 RNA-Seq:(High) - Functional Loss DEL TCGA 32..34 33 COAD,STAD,UCEC,CESC 9 - Human_RBP_ID_4852228,Human_RBP_ID_23051390,Human_RBP_ID_25933094 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 53904 RMVar_ID_53904 Human_SNP_ID_856761026 A-to-I Human chr5 - 131764234 131764234 131764234 GAGATTTGATGATTTATAAAGAAAAGAGGTTTAATTGGCTCATGGTTCTGTAGGCTGTGCAAGAA GAGATTTGATGATTTATAAAGAAAAGAGGTTTTATTGGCTCATGGTTCTGTAGGCTGTGCAAGAA T A FNIP1,AC008695.1 Ensembl:ENSG00000217128,Ensembl:ENSG00000273217 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line chr5:131764233..131764234 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - RMVar_hsa_circ_79178,RMVar_hsa_circ_234287,RMVar_hsa_circ_121732,RMVar_hsa_circ_234317 53905 RMVar_ID_53905 Human_SNP_ID_856768346 A-to-I Human chr5 - 141531453 141531453 141531453 AAAAAACTAGCCAGATGTGGTGCCGCATGCCTATAGTCCCAGCCACTTGGGAGACTGAGGTGGGT AAAAAACTAGCCAGATGTGGTGCCGCATGCCTGTAGTCCCAGCCACTTGGGAGACTGAGGTGGGT T C DIAPH1 Ensembl:ENSG00000131504 Protein coding intron GSE100210 HepG2 cell line chr5:141531452..141531453 29129909 RNA-Seq:(High) rs936049493 Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_97418,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_235085,RMVar_hsa_circ_235082,RMVar_hsa_circ_235083,RMVar_hsa_circ_235081,RMVar_hsa_circ_235078,RMVar_hsa_circ_235079,RMVar_hsa_circ_52474,RMVar_hsa_circ_91511,RMVar_hsa_circ_235088,RMVar_hsa_circ_235090,RMVar_hsa_circ_99524,RMVar_hsa_circ_235091 53906 RMVar_ID_53906 Human_SNP_ID_856788270 A-to-I Human chr5 - 112329757 112329757 112329757 TATTTCCCCCACAATGGCTTAGGTGTACTCAGATCCATTCACACCCCCTTTTTCCTGTAGAGAGT TATTTCCCCCACAATGGCTTAGGTGTACTCAGGTCCATTCACACCCCCTTTTTCCTGTAGAGAGT T C EPB41L4A Ensembl:ENSG00000129595 Protein coding intron GSE100210 HepG2 cell line chr5:112329756..112329757 29129909 RNA-Seq:(High) rs997117503 Functional Loss SNV ICGC 33..33 33 BOCA 1 - 53907 RMVar_ID_53907 Human_SNP_ID_856830190 A-to-I Human chr5 - 94397439 94397439 94397439 TGTAAAAACTAGGTCCAACACATATTTGAATAATCTTCTAAGGCTGTTGCATTAAATAAGATCAT TGTAAAAACTAGGTCCAACACATATTTGAATAGTCTTCTAAGGCTGTTGCATTAAATAAGATCAT T C KIAA0825 Ensembl:ENSG00000185261 Protein coding intron GSE100210 HepG2 cell line chr5:94397438..94397439 29129909 RNA-Seq:(High) rs1360711278 Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 2 ovary RMVar_hsa_circ_334136,RMVar_hsa_circ_339227,RMVar_hsa_circ_345493,RMVar_hsa_circ_366972,RMVar_hsa_circ_342366,RMVar_hsa_circ_338433,RMVar_hsa_circ_301500,RMVar_hsa_circ_312233,RMVar_hsa_circ_291424,RMVar_hsa_circ_295069,RMVar_hsa_circ_291069,RMVar_hsa_circ_42479,RMVar_hsa_circ_233264,RMVar_hsa_circ_233266,RMVar_hsa_circ_233268,RMVar_hsa_circ_233269,RMVar_hsa_circ_233267,RMVar_hsa_circ_233265,RMVar_hsa_circ_233262,RMVar_hsa_circ_233263,RMVar_hsa_circ_67067,RMVar_hsa_circ_346080 53908 RMVar_ID_53908 Human_SNP_ID_856848418 A-to-I Human chr5 - 127511656 127511656 127511656 CTACTGCACAAGTAACTATTCCCAAAGATTTGACTGGATCTATTATTGGCAAAGGTGGTCAGCGG CTACTGCACAAGTAACTATTCCCAAAGATTTGGCTGGATCTATTATTGGCAAAGGTGGTCAGCGG T C HNRNPKP1 Ensembl:ENSG00000250859 Pseudogene exon GSE100210 HepG2 cell line chr5:127511655..127511656 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 2 - 53909 RMVar_ID_53909 Human_SNP_ID_856857689 A-to-I Human chr5 + 141123415 141123415 141123415 ACAACAGCCCCGCCCTGCACATCGGCAGTGTCAGCGCCACAGACAGAGACTCGGGCACCAACGCC ACAACAGCCCCGCCCTGCACATCGGCAGTGTCCGCGCCACAGACAGAGACTCGGGCACCAACGCC A C PCDHB4 Ensembl:ENSG00000081818 Protein coding exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr5:141123414..141123415 30559470 RNA-Seq:(High) rs782542981 Functional Loss SNV ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,breast metaplastic_carcinoma,pancreas ductal_carcinoma,LAML,lung adenocarcinoma,lung large_cell_carcinoma,lung non_small_cell_carcinoma,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 19 lung,pancreas,haematopoietic and lymphoid tissue,breast 53910 RMVar_ID_53910 Human_SNP_ID_856874233 A-to-I Human chr5 - 132916190 132916190 132916190 CTGTCACCCAGGCTAGAGTGCAGTGGCATGATATCAGCTCATTGCAACCTCCGCTTCCCAAGCTC CTGTCACCCAGGCTAGAGTGCAGTGGCATGATGTCAGCTCATTGCAACCTCCGCTTCCCAAGCTC T C AFF4 Ensembl:ENSG00000072364 Protein coding intron GSE38233 cultured B-cells chr5:132916189..132916190 24183664 RNA-Seq:(High) rs1173410298 Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_99039,RMVar_hsa_circ_234392,RMVar_hsa_circ_60074,RMVar_hsa_circ_80330,RMVar_hsa_circ_234399,RMVar_hsa_circ_268115,RMVar_hsa_circ_70765,RMVar_hsa_circ_268451,RMVar_hsa_circ_29131,RMVar_hsa_circ_69535,RMVar_hsa_circ_70682 53911 RMVar_ID_53911 Human_SNP_ID_856886675 A-to-I Human chr5 + 134900899 134900899 134900899 AACCTCTGCTTCCCGGGTTCAAGCGATTCTCCAGCCTCAGCCTCCTGAGTAGCTGGGACTATGGG AACCTCTGCTTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGGACTATGGG A T TXNDC15 Ensembl:ENSG00000113621 Protein coding 3'UTR GSE38233 cultured B-cells chr5:134900898..134900899 24183664 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 1 prostate 53912 RMVar_ID_53912 Human_SNP_ID_856926754 A-to-I Human chr5 + 176093755 176093755 176093755 ATTTATTTTCTGTCGTTACAGACATCCTTGGGAGTTCCACAATGTGGTACGTATTGGGGAACCCC ATTTATTTTCTGTCGTTACAGACATCCTTGGGCGTTCCACAATGTGGTACGTATTGGGGAACCCC A C AC139491.7,FAM153B Ensembl:ENSG00000285476,Ensembl:ENSG00000182230 Protein coding,Protein coding CDS,CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr5:176093754..176093755 30559470 RNA-Seq:(High) rs756424964 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 11 haematopoietic and lymphoid tissue Human_Splice_Rec_722244,Human_Splice_Rec_722245,Human_Splice_Rec_722342,Human_Splice_Rec_722343,Human_Splice_Rec_722386,Human_Splice_Rec_722387,Human_Splice_Rec_722416,Human_Splice_Rec_722417,Human_Splice_Rec_722448,Human_Splice_Rec_722449,Human_Splice_Rec_722464,Human_Splice_Rec_722465,Human_Splice_Rec_722508,Human_Splice_Rec_722509 53913 RMVar_ID_53913 Human_SNP_ID_856958477 A-to-I Human chr5 + 131288531 131288531 131288531 GATTCCTTTTTTTTTAGAGAGAGCCTCACTCTATGGTCCAGGCTGAAGTGCAGTGGTGCAGTCAT GATTCCTTTTTTTTTAGAGAGAGCCTCACTCTGTGGTCCAGGCTGAAGTGCAGTGGTGCAGTCAT A G CDC42SE2 Ensembl:ENSG00000158985 Protein coding intron GSE38233 cultured B-cells chr5:131288530..131288531 24183664 RNA-Seq:(High) rs1004578319 Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_329116 53914 RMVar_ID_53914 Human_SNP_ID_856967312 A-to-I Human chr5 + 115390635 115390635 115390635 TTCCACAGCTGCTTCTGCTTGCTCAGTAAAACATGGCATGACTGTGTTGGAAAGCAGCTTAGTGG TTCCACAGCTGCTTCTGCTTGCTCAGTAAAACGTGGCATGACTGTGTTGGAAAGCAGCTTAGTGG A G - - Other Unknown GSE100210 HepG2 cell line chr5:115390634..115390635 29129909 RNA-Seq:(High) rs879118692 Functional Loss SNV ICGC 33..33 33 LAML 2 - 53915 RMVar_ID_53915 Human_SNP_ID_856970577 A-to-I Human chr5 - 128259552 128259550 128259553 GGAAATCACTAGCATCCCTCTCTACAAGAAGAAGGAGCTTAAGAAACTGGAAGAGAGCAATGAGG GGAAATCACTAGCATCCCTCTCTACAAGAAG___GAGCTTAAGAAACTGGAAGAGAGCAATGAGG CCTT C FBN2 Ensembl:ENSG00000138829 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector chr5:128259551..128259552 29967493 RNA-Seq:(High) rs1372300289 Functional Loss DEL ICGC 32..34 33 LICA 1 - Human_RBP_ID_1985712 Human_miRNA_ID_2069889,Human_miRNA_ID_2802789 RMVar_hsa_circ_106285,RMVar_hsa_circ_234163,RMVar_hsa_circ_90055,RMVar_hsa_circ_234162 53916 RMVar_ID_53916 Human_SNP_ID_856972775 A-to-I Human chr5 + 277562 277562 277562 TGACCTCATGATCCACCCGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCACGC TGACCTCATGATCCACCCGCCTCAGCCTCCCAGAGTGCTGGGATTACAGGCGTGAGCCACCACGC A G AHRR,AC021087.5,PDCD6 Ensembl:ENSG00000286169,Ensembl:ENSG00000286001,Ensembl:ENSG00000249915 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line chr5:277562..277563 29129909 RNA-Seq:(High) rs886491804 Functional Loss SNV ICGC 33..33 33 CMDI 1 - RMVar_hsa_circ_36209,RMVar_hsa_circ_114576,RMVar_hsa_circ_109933,RMVar_hsa_circ_229942,RMVar_hsa_circ_229943,RMVar_hsa_circ_31940 53917 RMVar_ID_53917 Human_SNP_ID_856982291 A-to-I Human chr5 - 662915 662915 662915 CGGACTCACCCGATCACAGACGAGCGGTCACCAGAATCGCCCGATCACAGACGAGCAGTCATCGG CGGACTCACCCGATCACAGACGAGCGGTCACCGGAATCGCCCGATCACAGACGAGCAGTCATCGG T C TPPP Ensembl:ENSG00000171368 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank chr5:662914..662915 30559470 RNA-Seq:(High) rs878950282 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 2 large intestine RMVar_hsa_circ_78820,RMVar_hsa_circ_229975 53918 RMVar_ID_53918 Human_SNP_ID_857261223 A-to-I Human chr5 + 61367859 61367859 61367859 AAAGTTGTTTGTGGCTGGGCATAGTGGCTCACACCTGTAATCCCAACATTTTGGGAGGCCAAGAT AAAGTTGTTTGTGGCTGGGCATAGTGGCTCACCCCTGTAATCCCAACATTTTGGGAGGCCAAGAT A C ZSWIM6 Ensembl:ENSG00000130449 Protein coding intron GSE100210 HepG2 cell line chr5:61367858..61367859 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_231636,RMVar_hsa_circ_89533 53919 RMVar_ID_53919 Human_SNP_ID_857263214 A-to-I Human chr5 + 61375503 61375503 61375503 TTCTGAAGATGAGGATAAGAAACAAGGAAAACAGAGAAAGAAAAAGAAGAACCGTTCACATAAAT TTCTGAAGATGAGGATAAGAAACAAGGAAAACGGAGAAAGAAAAAGAAGAACCGTTCACATAAAT A G ZSWIM6,AC122718.1 Ensembl:ENSG00000130449,Ensembl:ENSG00000250461 Protein coding,Pseudogene intron,exon GSE107867 ASD brains,frontal_cortex chr5:61375502..61375503 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue Human_RBP_ID_5103405,Human_RBP_ID_18538420 RMVar_hsa_circ_231636,RMVar_hsa_circ_89533 53920 RMVar_ID_53920 Human_SNP_ID_857274410 A-to-I Human chr5 - 172109060 172109060 172109060 ATCAGTAAGGCCGGGCGCAGTGGCTCACGCCTATAATCCCAGCACTTTGGAAGGCCAAGGCTGGT ATCAGTAAGGCCGGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGAAGGCCAAGGCTGGT T C STK10 Ensembl:ENSG00000072786 Protein coding intron GSE38233 cultured B-cells chr5:172109059..172109060 24183664 RNA-Seq:(High) rs865828701 Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 1 prostate 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_28961,RMVar_hsa_circ_268016,RMVar_hsa_circ_15818,RMVar_hsa_circ_378668 53921 RMVar_ID_53921 Human_SNP_ID_857351137 A-to-I Human chr5 - 22270869 22270869 22270869 GAGTTCAAGACTAGCCTGGCCAACATGGTGAAACCCTATCTGTACTAAATACACAAAAAATTAGC GAGTTCAAGACTAGCCTGGCCAACATGGTGAAGCCCTATCTGTACTAAATACACAAAAAATTAGC T C CDH12 Ensembl:ENSG00000154162 Protein coding intron GSE47997 K562 cells&HepG2 cells chr5:22270868..22270869 23474544 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 kidney clear_cell_renal_cell_carcinoma 2 kidney 53922 RMVar_ID_53922 Human_SNP_ID_857431088 A-to-I Human chr5 + 122027179 122027179 122027179 CTTTTCCATCTAAAAAAAAAAATGTTTTTTTTAAGACAGGATCTCATTCTGTTGCCCAGACTAGA CTTTTCCATCTAAAAAAAAAAATGTTTTTTTTGAGACAGGATCTCATTCTGTTGCCCAGACTAGA A G SRFBP1 Ensembl:ENSG00000151304 Protein coding 3'UTR GSE47997;GSE38233;GSE38233;GSE100210;GSE99789;GSE99789;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831 K562 cells&HepG2 cells;cultured B-cells;cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109;ASD brains,Fragile X samples from NIH NeuroBioBank;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line chr5:122027178..122027179;chr5:122027179..122027180 23474544,24183664,24183664,29129909,29796672,29796672,30559470,31158229,31158229,31158229,31158229,31158229,32596459 RNA-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_1985153,Human_RBP_ID_22404137 RMVar_hsa_circ_233992 53923 RMVar_ID_53923 Human_SNP_ID_857431112 A-to-I Human chr5 + 122027179 122027179 122027179 CTTTTCCATCTAAAAAAAAAAATGTTTTTTTTAAGACAGGATCTCATTCTGTTGCCCAGACTAGA CTTTTCCATCTAAAAAAAAAAATGTTTTTTTTTAGACAGGATCTCATTCTGTTGCCCAGACTAGA A T SRFBP1 Ensembl:ENSG00000151304 Protein coding 3'UTR GSE47997;GSE38233;GSE38233;GSE100210;GSE99789;GSE99789;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831 K562 cells&HepG2 cells;cultured B-cells;cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,EC109;ASD brains,Fragile X samples from NIH NeuroBioBank;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line chr5:122027178..122027179;chr5:122027179..122027180 23474544,24183664,24183664,29129909,29796672,29796672,30559470,31158229,31158229,31158229,31158229,31158229,32596459 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_1985153,Human_RBP_ID_22404137 RMVar_hsa_circ_233992 53924 RMVar_ID_53924 Human_SNP_ID_857441095 A-to-I Human chr5 - 88188167 88188167 88188167 CTGGGAGGCGGAGGTTGCAGTGAGCTGAGATCATGCCACTCTACTCCAGCCTGGGCAACAAGAGT CTGGGAGGCGGAGGTTGCAGTGAGCTGAGATCGTGCCACTCTACTCCAGCCTGGGCAACAAGAGT T C - - Other Unknown GSE100210 HepG2 cell line chr5:88188166..88188167 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - Human_RBP_ID_25944960 53925 RMVar_ID_53925 Human_SNP_ID_857448944 A-to-I Human chr5 - 59178903 59178903 59178903 ATGAACCTGTACCTGAGGCCTCTAGTGAGAGAAGCCACATGGAAGCTGGTCTTCACGCTGCTCCA ATGAACCTGTACCTGAGGCCTCTAGTGAGAGACGCCACATGGAAGCTGGTCTTCACGCTGCTCCA T G PDE4D Ensembl:ENSG00000113448 Protein coding intron GSE100210 HepG2 cell line chr5:59178902..59178903 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_324536,RMVar_hsa_circ_330021,RMVar_hsa_circ_7785,RMVar_hsa_circ_324797,RMVar_hsa_circ_32204,RMVar_hsa_circ_297202,RMVar_hsa_circ_335160 53926 RMVar_ID_53926 Human_SNP_ID_857475823 A-to-I Human chr5 - 43582337 43582337 43582337 TCTGTGCCATTTCTCCTATTAAGCTGCCTTTTATCAGTTGATTTTTCAGTGGACCTTCAGAGGGC TCTGTGCCATTTCTCCTATTAAGCTGCCTTTTGTCAGTTGATTTTTCAGTGGACCTTCAGAGGGC T C NNT-AS1 Ensembl:ENSG00000248092 lincRNA intron GSE100210 HepG2 cell line chr5:43582336..43582337 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 CLLE 1 - Human_RBP_ID_17575390 53927 RMVar_ID_53927 Human_SNP_ID_857758587 A-to-I Human chr5 - 132474627 132474625 132474628 CCAGTGTAATCACAAGGGTTCTTAAATGAAGAAGGAGGAGGCAGAAGGGTCAGAACCAGAGAGAT CCAGTGTAATCACAAGGGTTCTTAAATGAAG___GAGGAGGCAGAAGGGTCAGAACCAGAGAGAT CCTT C - - Other Unknown GSE100210 HepG2 cell line chr5:132474626..132474627 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 32..34 33 RECA 1 - 53928 RMVar_ID_53928 Human_SNP_ID_857798371 A-to-I Human chr5 - 157477823 157477823 157477823 GTATTGCCATAGTCCCTTCCCCCTGAAGCAATAGCCCCTCCCCACCTCCTGCAATACGCCTTTCC GTATTGCCATAGTCCCTTCCCCCTGAAGCAATGGCCCCTCCCCACCTCCTGCAATACGCCTTTCC T C ADAM19 Ensembl:ENSG00000135074 Protein coding intron GSE38233;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,KYSE180 cell line chr5:157477822..157477823 24183664,32596459 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue RMVar_hsa_circ_118709,RMVar_hsa_circ_235821,RMVar_hsa_circ_235822,RMVar_hsa_circ_76268 53929 RMVar_ID_53929 Human_SNP_ID_857822699 A-to-I Human chr5 - 180795798 180795796 180795798 ACCGAGGAATTCAGGGCAAACAGATCATCTCAATTTGCCTTGCTGATGTGCCAGCTGGGATTACG ACCGAGGAATTCAGGGCAAACAGATCATCTCA__TTGCCTTGCTGATGTGCCAGCTGGGATTACG AAT A MGAT1 Ensembl:ENSG00000131446 Protein coding intron GSE38233 cultured B-cells chr5:180795797..180795798 24183664 RNA-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 53930 RMVar_ID_53930 Human_SNP_ID_857844050 A-to-I Human chr5 - 14847939 14847939 14847939 GGGGTTTCACCACGTTGGCCAGGCTGGTCTCAAACTCCTGACCTCAAGTTATCCGCCCACCTCAG GGGGTTTCACCACGTTGGCCAGGCTGGTCTCATACTCCTGACCTCAAGTTATCCGCCCACCTCAG T A ANKH Ensembl:ENSG00000154122 Protein coding intron GSE47997 K562 cells&HepG2 cells chr5:14847938..14847939 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 53931 RMVar_ID_53931 Human_SNP_ID_857845104 A-to-I Human chr5 + 65822923 65822923 65822923 GAGTAGAGGCCTGCATGCTCCGTGAACTGGGGATCTTTGGTAGCCGTCCATGTCTGGAGGACAAG GAGTAGAGGCCTGCATGCTCCGTGAACTGGGGGTCTTTGGTAGCCGTCCATGTCTGGAGGACAAG A G NLN Ensembl:ENSG00000123213 Protein coding 3'UTR GSE100210 HepG2 cell line chr5:65822922..65822923 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine Human_RBP_ID_644691,Human_RBP_ID_787787,Human_RBP_ID_1042058,Human_RBP_ID_7459040,Human_RBP_ID_8891222,Human_RBP_ID_15490540,Human_RBP_ID_27083292 Human_miRNA_ID_2256678 RMVar_hsa_circ_231906,RMVar_hsa_circ_93753 53932 RMVar_ID_53932 Human_SNP_ID_857857481 A-to-I Human chr5 + 140854001 140854000 140854002 TTGAGACCAATGTAGTGAGACTCATCTCTGCCAAAAAAAAAAAATTAGCCGGGCATGGTGGCACA TTGAGACCAATGTAGTGAGACTCATCTCTGCC__AAAAAAAAAATTAGCCGGGCATGGTGGCACA CAA C PCDHA5,PCDHA3,PCDHA4,PCDHA9,PCDHA7,PCDHA8,PCDHA1,PCDHA6,PCDHA2 Ensembl:ENSG00000204965,Ensembl:ENSG00000255408,Ensembl:ENSG00000204967,Ensembl:ENSG00000204961,Ensembl:ENSG00000204963,Ensembl:ENSG00000204962,Ensembl:ENSG00000204970,Ensembl:ENSG00000081842,Ensembl:ENSG00000204969 Protein coding,Protein coding,Protein coding,Protein coding,Protein coding,Protein coding,Protein coding,Protein coding,Protein coding intron,intron,intron,3'UTR,intron,intron,intron,intron,intron GSE47997 K562 cells&HepG2 cells chr5:140854001..140854002 23474544 RNA-Seq:(High) - Functional Loss DEL TCGA 33..34 33 COAD 1 - RMVar_hsa_circ_235058 53933 RMVar_ID_53933 Human_SNP_ID_857878409 A-to-I Human chr5 + 25910828 25910828 25910828 AACTGGCCCGACAGAAGAAAGAGAGTGAGGCTATGGAGTGGCAGCAGAAGGCCCAGATGGTACAG AACTGGCCCGACAGAAGAAAGAGAGTGAGGCTGTGGAGTGGCAGCAGAAGGCCCAGATGGTACAG A G MSNP1 Ensembl:ENSG00000251593 Pseudogene exon GSE100210 HepG2 cell line chr5:25910827..25910828 29129909 RNA-Seq:(High) rs964252428 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_26525741 53934 RMVar_ID_53934 Human_SNP_ID_858014484 A-to-I Human chr5 + 176308192 176308192 176308192 AAGTGATGGGGCTGTGGATAGGGGAGTTGAACAATGATACAAGGAGTGACTCCAAATTTGCATAT AAGTGATGGGGCTGTGGATAGGGGAGTTGAACGATGATACAAGGAGTGACTCCAAATTTGCATAT A G BRCC3P1,SIMC1 Ensembl:ENSG00000251667,Ensembl:ENSG00000170085 Pseudogene,Protein coding exon,intron GSE100210 HepG2 cell line chr5:176308191..176308192 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 10 haematopoietic and lymphoid tissue Human_RBP_ID_10232284,Human_RBP_ID_22727373 Human_miRNA_ID_1880571,Human_miRNA_ID_1902726 RMVar_hsa_circ_58004,RMVar_hsa_circ_63765,RMVar_hsa_circ_306548,RMVar_hsa_circ_309390,RMVar_hsa_circ_236342,RMVar_hsa_circ_322535 53935 RMVar_ID_53935 Human_SNP_ID_858159319 A-to-I Human chr5 - 149531477 149531477 149531477 TTTTGTTCTTGTTGCCCAGGCAGGAGTGCAATAGCGTGATCTCGGCTCACTGCAACCTCGGCCTC TTTTGTTCTTGTTGCCCAGGCAGGAGTGCAATTGCGTGATCTCGGCTCACTGCAACCTCGGCCTC T A CSNK1A1 Ensembl:ENSG00000113712 Protein coding intron GSE38233 cultured B-cells chr5:149531476..149531477 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 6 oesophagus Human_Splice_Rec_708686,Human_Splice_Rec_708736 RMVar_hsa_circ_310903,RMVar_hsa_circ_265447,RMVar_hsa_circ_235404 53936 RMVar_ID_53936 Human_SNP_ID_858165210 A-to-I Human chr5 + 14191429 14191428 14191429 GCCTGGGTAGCATAGCTAGACTCTATCGCTACAAAAAAATGAAAATATTTAGCTGGCCGTGGTGG GCCTGGGTAGCATAGCTAGACTCTATCGCTAC_AAAAAATGAAAATATTTAGCTGGCCGTGGTGG CA C TRIO Ensembl:ENSG00000038382 Protein coding intron GSE47997 K562 cells&HepG2 cells chr5:14191428..14191429 23474544 RNA-Seq:(High) - Functional Loss DEL ICGC 33..33 33 PAAD 1 - Human_RBP_ID_2902331 RMVar_hsa_circ_77339,RMVar_hsa_circ_94247,RMVar_hsa_circ_93187,RMVar_hsa_circ_230320,RMVar_hsa_circ_230321,RMVar_hsa_circ_230319 53937 RMVar_ID_53937 Human_SNP_ID_858181971 A-to-I Human chr5 - 112329763 112329763 112329763 TGAAAGTATTTCCCCCACAATGGCTTAGGTGTACTCAGATCCATTCACACCCCCTTTTTCCTGTA TGAAAGTATTTCCCCCACAATGGCTTAGGTGTGCTCAGATCCATTCACACCCCCTTTTTCCTGTA T C EPB41L4A Ensembl:ENSG00000129595 Protein coding intron GSE100210 HepG2 cell line chr5:112329762..112329763 29129909 RNA-Seq:(High) rs1335724359 Functional Loss SNV ICGC,COSMIC 33..33 33 NKTL,haematopoietic_and_lymphoid_tissue NK-T_cell_lymphoma 3 haematopoietic and lymphoid tissue 53938 RMVar_ID_53938 Human_SNP_ID_858190080 A-to-I Human chr5 + 132351772 132351772 132351772 ACTGGATTCTACATATGTTGAAATTATGGCAAAAGACTTTATTGACAGATTGGATGTGGAGTACG ACTGGATTCTACATATGTTGAAATTATGGCAACAGACTTTATTGACAGATTGGATGTGGAGTACG A C lnc-SLC22A5-1 RNACentral:URS00008B5099 lincRNA intron GSE100210 HepG2 cell line chr5:132351772..132351773 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 53939 RMVar_ID_53939 Human_SNP_ID_858191573 A-to-I Human chr5 - 159203632 159203631 159203633 AATTTTAGGTCTTCTCCAAGAAAAAAAAAAAGAAAAAAAAAAACAACATGGCTGCAAAGGAGAAA AATTTTAGGTCTTCTCCAAGAAAAAAAAAAA__AAAAAAAAAACAACATGGCTGCAAAGGAGAAA TTC T RNF145 Ensembl:ENSG00000145860 Protein coding CDS GSE38233 cultured B-cells chr5:159203632..159203633 24183664 RNA-Seq:(High) - Functional Loss DEL TCGA 32..33 33 COAD,STAD,UCS,LIHC,UCEC,ESCA,THYM 26 - Human_RBP_ID_4852228,Human_RBP_ID_23051390,Human_RBP_ID_25933094 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 53940 RMVar_ID_53940 Human_SNP_ID_858253208 A-to-I Human chr5 + 69174936 69174936 69174936 CAGCTGGTTGGTGTCACTGCCATGTTTATTGCAAGCAAATATGAAGAAATGTACCCTCCAGAAAT CAGCTGGTTGGTGTCACTGCCATGTTTATTGCTAGCAAATATGAAGAAATGTACCCTCCAGAAAT A T CCNB1 Ensembl:ENSG00000134057 Protein coding CDS GSE100210 HepG2 cell line chr5:69174936..69174937 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 2 prostate Human_RBP_ID_1657119,Human_RBP_ID_1998570,Human_RBP_ID_8620952,Human_RBP_ID_9397862,Human_RBP_ID_18846085,Human_RBP_ID_19014887,Human_RBP_ID_22099435,Human_RBP_ID_24113999,Human_RBP_ID_27516990 Human_Splice_Rec_658004,Human_Splice_Rec_658018,Human_Splice_Rec_658032,Human_Splice_Rec_658042,Human_Splice_Rec_658056 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 53941 RMVar_ID_53941 Human_SNP_ID_858334972 A-to-I Human chr5 + 131289893 131289893 131289893 ACAGGGACTCGCTCTGTCACCTAAGCTGTAGTAGAGTGGCACAGTCATAACTCACTACTGCAGCC ACAGGGACTCGCTCTGTCACCTAAGCTGTAGTGGAGTGGCACAGTCATAACTCACTACTGCAGCC A G CDC42SE2 Ensembl:ENSG00000158985 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr5:131289892..131289893 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 5 breast Human_RBP_ID_22613137 RMVar_hsa_circ_329116 53942 RMVar_ID_53942 Human_SNP_ID_858357927 A-to-I Human chr5 - 149932504 149932504 149932504 CCAAATGCTAGCGTGATAATAATGCAAGTTCCAGAGAGGATTGTTGTAGCAGGAAATAATGAGGA CCAAATGCTAGCGTGATAATAATGCAAGTTCCGGAGAGGATTGTTGTAGCAGGAAATAATGAGGA T C PDE6A,MFFP2 Ensembl:ENSG00000132915,Ensembl:ENSG00000251583 Protein coding,Pseudogene intron,exon GSE38233 cultured B-cells chr5:149932503..149932504 24183664 RNA-Seq:(High) rs75204652 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 8 haematopoietic and lymphoid tissue RMVar_hsa_circ_25484 53943 RMVar_ID_53943 Human_SNP_ID_858382070 A-to-I Human chr5 - 159203632 159203632 159203632 AATTTTAGGTCTTCTCCAAGAAAAAAAAAAAGAAAAAAAAAAACAACATGGCTGCAAAGGAGAAA AATTTTAGGTCTTCTCCAAGAAAAAAAAAAAGGAAAAAAAAAACAACATGGCTGCAAAGGAGAAA T C RNF145 Ensembl:ENSG00000145860 Protein coding CDS GSE38233 cultured B-cells chr5:159203632..159203633 24183664 RNA-Seq:(High) rs765426233 Functional Loss SNV ICGC,COSMIC 33..33 33 biliary_tract adenocarcinoma,pancreas ductal_carcinoma,caecum adenocarcinoma,COCA,gallbladder adenocarcinoma,large_intestine adenocarcinoma,endometrium endometrioid_carcinoma 66 biliary tract,caecum,uterus,gallbladder,pancreas,large intestine Human_RBP_ID_4852228,Human_RBP_ID_23051390,Human_RBP_ID_25933094 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 53944 RMVar_ID_53944 Human_SNP_ID_858403874 A-to-I Human chr5 + 128110761 128110761 128110761 ACCTGAGCGATCTGCTAGAAAAACTTAAATGGACAAAAGATCACAATGAAGAGGCCAAAAAGATA ACCTGAGCGATCTGCTAGAAAAACTTAAATGGGCAAAAGATCACAATGAAGAGGCCAAAAAGATA A G SLC12A2,KDELC1P1 Ensembl:ENSG00000064651,Ensembl:ENSG00000250329 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line chr5:128110760..128110761 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue RMVar_hsa_circ_100540,RMVar_hsa_circ_234127 53945 RMVar_ID_53945 Human_SNP_ID_858421336 A-to-I Human chr5 - 43045347 43045347 43045347 GATGCCATTTTTCCTTTATTCTCCCGTCTGTAAGACCAGAAGGCAATTGGAGGATCCTCAAATAC GATGCCATTTTTCCTTTATTCTCCCGTCTGTATGACCAGAAGGCAATTGGAGGATCCTCAAATAC T A AC025171.1 Ensembl:ENSG00000177738 lincRNA intron GSE100210 HepG2 cell line chr5:43045346..43045347 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 RECA 1 - Human_RBP_ID_5617079 53946 RMVar_ID_53946 Human_SNP_ID_858432859 A-to-I Human chr5 - 176913785 176913785 176913785 TTTGTAGAGACGGGGGTTTCACCCTGTTGCCCAGGCTGTTCTCGAACTCCTGGTCTCAAGTGATC TTTGTAGAGACGGGGGTTTCACCCTGTTGCCCGGGCTGTTCTCGAACTCCTGGTCTCAAGTGATC T C UIMC1 Ensembl:ENSG00000087206 Protein coding intron GSE100210 HepG2 cell line chr5:176913784..176913785 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 5 pancreas 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_236399 53947 RMVar_ID_53947 Human_SNP_ID_858498281 A-to-I Human chr5 + 176308801 176308801 176308801 CCCAAGATCCTGTGCCAGGAGGAGCAGGATGCATATTGGAGGATCCACAGCCTTACACATCTGGA CCCAAGATCCTGTGCCAGGAGGAGCAGGATGCGTATTGGAGGATCCACAGCCTTACACATCTGGA A G BRCC3P1,SIMC1 Ensembl:ENSG00000251667,Ensembl:ENSG00000170085 Pseudogene,Protein coding exon,intron GSE100210 HepG2 cell line chr5:176308800..176308801 29129909 RNA-Seq:(High) rs529194638 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 10 haematopoietic and lymphoid tissue Human_RBP_ID_18838746 RMVar_hsa_circ_58004,RMVar_hsa_circ_63765,RMVar_hsa_circ_306548,RMVar_hsa_circ_309390,RMVar_hsa_circ_236342,RMVar_hsa_circ_322535 53948 RMVar_ID_53948 Human_SNP_ID_858529785 A-to-I Human chr5 + 61367940 61367940 61367940 GAACAGGAGTTTGAGACCAGCCTCTGTAACATAGGGAGGCCTCCATCTCTACAAAAAATTAAAAA GAACAGGAGTTTGAGACCAGCCTCTGTAACATGGGGAGGCCTCCATCTCTACAAAAAATTAAAAA A G ZSWIM6 Ensembl:ENSG00000130449 Protein coding intron GSE100210 HepG2 cell line chr5:61367939..61367940 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_15478016 RMVar_hsa_circ_231636,RMVar_hsa_circ_89533 53949 RMVar_ID_53949 Human_SNP_ID_858549581 A-to-I Human chr5 - 75377997 75377997 75377997 AGGTGGGAGAATGGCTTGAGGCCAGGAGTTCAAGTCTAGCCTGGATAACATAGCAAGATTCCATC AGGTGGGAGAATGGCTTGAGGCCAGGAGTTCAGGTCTAGCCTGGATAACATAGCAAGATTCCATC T C CERT1 Ensembl:ENSG00000113163 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr5:75377996..75377997 24183664,29129909 RNA-Seq:(High) rs775637134 Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 12 breast RMVar_hsa_circ_269711 53950 RMVar_ID_53950 Human_SNP_ID_858558025 A-to-I Human chr5 + 115390654 115390654 115390654 TGCTCAGTAAAACATGGCATGACTGTGTTGGAAAGCAGCTTAGTGGCTTCCAGAACCTTCTCTGT TGCTCAGTAAAACATGGCATGACTGTGTTGGAGAGCAGCTTAGTGGCTTCCAGAACCTTCTCTGT A G - - Other Unknown GSE100210 HepG2 cell line chr5:115390654..115390655 29129909 RNA-Seq:(High) rs111866497 Functional Loss SNV ICGC 33..33 33 LAML 1 - 53951 RMVar_ID_53951 Human_SNP_ID_858591820 A-to-I Human chr5 - 75378047 75378047 75378047 GCCAGGTGCAGTGGGTCACACCTGTAATCCCAACACTTTTTGGGAGACTGAGGTGGGAGAATGGC GCCAGGTGCAGTGGGTCACACCTGTAATCCCAGCACTTTTTGGGAGACTGAGGTGGGAGAATGGC T C CERT1 Ensembl:ENSG00000113163 Protein coding intron GSE38233 cultured B-cells chr5:75378046..75378047 24183664 RNA-Seq:(High) rs963099315 Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 11 liver RMVar_hsa_circ_269711 53952 RMVar_ID_53952 Human_SNP_ID_858764234 A-to-I Human chr5 + 134779644 134779644 134779644 CTTCAACCTTCTTAGTAGTTAGGACTACAGGCATGTACCACCACATCTGGCTAATTGTTTATAGA CTTCAACCTTCTTAGTAGTTAGGACTACAGGCTTGTACCACCACATCTGGCTAATTGTTTATAGA A T DDX46 Ensembl:ENSG00000145833 Protein coding intron GSE100210 HepG2 cell line chr5:134779643..134779644 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 4 oesophagus Human_RBP_ID_8602919,Human_RBP_ID_15303391 RMVar_hsa_circ_55145,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_67576,RMVar_hsa_circ_309182,RMVar_hsa_circ_348128,RMVar_hsa_circ_351802,RMVar_hsa_circ_234598,RMVar_hsa_circ_361622,RMVar_hsa_circ_350703,RMVar_hsa_circ_334557,RMVar_hsa_circ_339485,RMVar_hsa_circ_317403,RMVar_hsa_circ_71038,RMVar_hsa_circ_75281,RMVar_hsa_circ_69003,RMVar_hsa_circ_234599,RMVar_hsa_circ_234600 53953 RMVar_ID_53953 Human_SNP_ID_858807246 A-to-I Human chr5 + 172993253 172993253 172993253 AAGAAAATACACACACAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAAGCATAGGTAGGTGG AAGAAAATACACACACAGTGGCTCATGCCTGTGATCCCAGCACTTTGGGAAGCATAGGTAGGTGG A G ATP6V0E1 Ensembl:ENSG00000113732 Protein coding intron GSE38233 cultured B-cells chr5:172993252..172993253 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - RMVar_hsa_circ_236281,RMVar_hsa_circ_127736 53954 RMVar_ID_53954 Human_SNP_ID_858815787 A-to-I Human chr5 - 177337234 177337234 177337234 GTGCTGGGCCCTGCAGGTGATGACCGACCTGGAGGACAAGAACGAGTGGAAGAACTGCATTGACA GTGCTGGGCCCTGCAGGTGATGACCGACCTGGTGGACAAGAACGAGTGGAAGAACTGCATTGACA T A LMAN2 Ensembl:ENSG00000169223 Protein coding CDS GSE100210 HepG2 cell line chr5:177337233..177337234 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_RBP_ID_947081,Human_RBP_ID_1651312,Human_RBP_ID_1993069,Human_RBP_ID_3766373,Human_RBP_ID_3968435,Human_RBP_ID_9399709,Human_RBP_ID_15399355,Human_RBP_ID_22771528,Human_RBP_ID_27514415 Human_Splice_Rec_724734,Human_Splice_Rec_724735,Human_Splice_Rec_724750,Human_Splice_Rec_724751,Human_Splice_Rec_724774,Human_Splice_Rec_724775,Human_Splice_Rec_724782,Human_Splice_Rec_724790 Human_miRNA_ID_2254426 RMVar_hsa_circ_106301,RMVar_hsa_circ_119385,RMVar_hsa_circ_123055,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_236477,RMVar_hsa_circ_236478,RMVar_hsa_circ_236476,RMVar_hsa_circ_109674,RMVar_hsa_circ_307525,RMVar_hsa_circ_236483,RMVar_hsa_circ_236484 53955 RMVar_ID_53955 Human_SNP_ID_858913427 A-to-I Human chr5 + 131187760 131187760 131187760 CACCTGCTTCAGCCCCCCAAAGTGCTGGTATTACATGCATGAGCCATTGCACCTGGCCTATAATT CACCTGCTTCAGCCCCCCAAAGTGCTGGTATTGCATGCATGAGCCATTGCACCTGGCCTATAATT A G LYRM7 Ensembl:ENSG00000186687 Protein coding intron GSE38233 cultured B-cells chr5:131187759..131187760 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 COCA 1 - RMVar_hsa_circ_75865,RMVar_hsa_circ_234222,RMVar_hsa_circ_123787,RMVar_hsa_circ_234225,RMVar_hsa_circ_234226,RMVar_hsa_circ_234227,RMVar_hsa_circ_80415,RMVar_hsa_circ_234229 53956 RMVar_ID_53956 Human_SNP_ID_858948830 A-to-I Human chr5 - 14797956 14797956 14797956 GTATCATCACAACAAAGACTCCTTCCAGTGATATTCTTGTCTTTGACTATACAAAACATCCTTCT GTATCATCACAACAAAGACTCCTTCCAGTGATGTTCTTGTCTTTGACTATACAAAACATCCTTCT T C ANKH,RBBP4P1 Ensembl:ENSG00000154122,Ensembl:ENSG00000249485 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line chr5:14797955..14797956 29129909 RNA-Seq:(High) rs1206325359 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue Human_RBP_ID_166356 53957 RMVar_ID_53957 Human_SNP_ID_859072285 A-to-I Human chr5 + 177047907 177047907 177047907 GTGATTCACCCGCTTCTGCCTCCCAAAGTGCTAGGATTACAGACATGAGCCACCGCACCTGGCCA GTGATTCACCCGCTTCTGCCTCCCAAAGTGCTGGGATTACAGACATGAGCCACCGCACCTGGCCA A G ZNF346 Ensembl:ENSG00000113761 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr5:177047906..177047907 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 6 prostate Human_RBP_ID_15395223 RMVar_hsa_circ_19708,RMVar_hsa_circ_80510,RMVar_hsa_circ_307082,RMVar_hsa_circ_236418,RMVar_hsa_circ_273241,RMVar_hsa_circ_236421,RMVar_hsa_circ_236422,RMVar_hsa_circ_59370,RMVar_hsa_circ_285547 53958 RMVar_ID_53958 Human_SNP_ID_859078554 A-to-I Human chr5 - 37209650 37209650 37209650 TAAATACCTTTTCTTTTGCCAAACCACTTTCTAGAAAGAAAACAGAAAGTGAATATTCACAGCCA TAAATACCTTTTCTTTTGCCAAACCACTTTCTGGAAAGAAAACAGAAAGTGAATATTCACAGCCA T C CPLANE1 Ensembl:ENSG00000197603 Protein coding intron GSE100210 HepG2 cell line chr5:37209649..37209650 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 haematopoietic and lymphoid tissue RMVar_hsa_circ_313599,RMVar_hsa_circ_37191,RMVar_hsa_circ_19407,RMVar_hsa_circ_36271,RMVar_hsa_circ_25842,RMVar_hsa_circ_230922,RMVar_hsa_circ_86106,RMVar_hsa_circ_230924,RMVar_hsa_circ_230925,RMVar_hsa_circ_38346,RMVar_hsa_circ_36226,RMVar_hsa_circ_304351,RMVar_hsa_circ_265172,RMVar_hsa_circ_28047,RMVar_hsa_circ_26337,RMVar_hsa_circ_230927,RMVar_hsa_circ_319381,RMVar_hsa_circ_230937,RMVar_hsa_circ_298314,RMVar_hsa_circ_284218,RMVar_hsa_circ_230943,RMVar_hsa_circ_12287,RMVar_hsa_circ_230941,RMVar_hsa_circ_230942,RMVar_hsa_circ_230940,RMVar_hsa_circ_40657,RMVar_hsa_circ_338561,RMVar_hsa_circ_292326,RMVar_hsa_circ_49570,RMVar_hsa_circ_230944,RMVar_hsa_circ_25476,RMVar_hsa_circ_285666,RMVar_hsa_circ_294837,RMVar_hsa_circ_72202,RMVar_hsa_circ_230949,RMVar_hsa_circ_230947,RMVar_hsa_circ_230948,RMVar_hsa_circ_345181,RMVar_hsa_circ_368892,RMVar_hsa_circ_49138,RMVar_hsa_circ_358673,RMVar_hsa_circ_14931,RMVar_hsa_circ_25205,RMVar_hsa_circ_7419,RMVar_hsa_circ_334456,RMVar_hsa_circ_230951,RMVar_hsa_circ_334936,RMVar_hsa_circ_299392,RMVar_hsa_circ_329552,RMVar_hsa_circ_9439,RMVar_hsa_circ_230952,RMVar_hsa_circ_230954,RMVar_hsa_circ_230955,RMVar_hsa_circ_230953,RMVar_hsa_circ_71306 53959 RMVar_ID_53959 Human_SNP_ID_859080715 A-to-I Human chr5 + 177172834 177172834 177172834 TTTTTAAAAACTAGCTGGGCATGGTGGTACATACCTTGTAGTCCCTGCTAGTTGGGAGGCTGAGG TTTTTAAAAACTAGCTGGGCATGGTGGTACATGCCTTGTAGTCCCTGCTAGTTGGGAGGCTGAGG A G NSD1 Ensembl:ENSG00000165671 Protein coding intron GSE100210 HepG2 cell line chr5:177172833..177172834 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_6376,RMVar_hsa_circ_109213,RMVar_hsa_circ_296651,RMVar_hsa_circ_322685,RMVar_hsa_circ_374749,RMVar_hsa_circ_236431,RMVar_hsa_circ_99866,RMVar_hsa_circ_236434,RMVar_hsa_circ_236435,RMVar_hsa_circ_236436,RMVar_hsa_circ_54322,RMVar_hsa_circ_325752,RMVar_hsa_circ_331791,RMVar_hsa_circ_97595,RMVar_hsa_circ_236437,RMVar_hsa_circ_236438 53960 RMVar_ID_53960 Human_SNP_ID_859164406 A-to-I Human chr5 - 146842720 146842720 146842720 AGAAAACCAAATATGGCATGTTCTCACTTATAAGTGGGAGCTAAATGATGAGAACACACGGATAC AGAAAACCAAATATGGCATGTTCTCACTTATAGGTGGGAGCTAAATGATGAGAACACACGGATAC T C PPP2R2B Ensembl:ENSG00000156475 Protein coding intron GSE100210 HepG2 cell line chr5:146842719..146842720 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_27564,RMVar_hsa_circ_294502,RMVar_hsa_circ_376514 53961 RMVar_ID_53961 Human_SNP_ID_859263828 A-to-I Human chr5 + 134900512 134900512 134900512 CCTGGCCAACTTGGTGAAACCCTCTCTCTACTAAAAATACAAAAAATTAGCTGGGCGTGGTGGCG CCTGGCCAACTTGGTGAAACCCTCTCTCTACTGAAAATACAAAAAATTAGCTGGGCGTGGTGGCG A G TXNDC15 Ensembl:ENSG00000113621 Protein coding 3'UTR GSE47997;GSE38233;GSE99789 K562 cells&HepG2 cells;cultured B-cells;esophageal squamous carcinoma cells,EC109 chr5:134900511..134900512;chr5:134900512..134900513 23474544,24183664,29796672 RNA-Seq:(High) rs145434259 Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 2 breast 53962 RMVar_ID_53962 Human_SNP_ID_859290358 A-to-I Human chr5 - 161523507 161523507 161523507 TTACATCTGAAATTGTTGTAATTTCAGATGTAAGAAAAGCAGGAAAGTCAGCAATGAACTAATGT TTACATCTGAAATTGTTGTAATTTCAGATGTACGAAAAGCAGGAAAGTCAGCAATGAACTAATGT T G GABRB2 Ensembl:ENSG00000145864 Protein coding intron GSE107867 ASD brains,cerebellum chr5:161523506..161523507 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 53963 RMVar_ID_53963 Human_SNP_ID_859346880 A-to-I Human chr5 - 115513266 115513266 115513266 TGACACACAAAGCATCGTGAAGGGATCGTTTCACCTCCTCAATGATCATCTTATTTCCTCCTCTG TGACACACAAAGCATCGTGAAGGGATCGTTTCGCCTCCTCAATGATCATCTTATTTCCTCCTCTG T C - - Other Unknown GSE100210 HepG2 cell line chr5:115513265..115513266 29129909 RNA-Seq:(High) rs878921173 Functional Loss SNV ICGC 33..33 33 ESCA 1 - 53964 RMVar_ID_53964 Human_SNP_ID_859379678 A-to-I Human chr5 - 151211761 151211761 151211761 TCAGCACTTTGGGAGGCTGAGGTGGGTGGATCACTTGAAGTCAGGAGTTTGAGACCTGCCTGGCC TCAGCACTTTGGGAGGCTGAGGTGGGTGGATCGCTTGAAGTCAGGAGTTTGAGACCTGCCTGGCC T C CCDC69 Ensembl:ENSG00000198624 Protein coding intron GSE38233 cultured B-cells chr5:151211760..151211761 24183664 RNA-Seq:(High) rs191676856 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 53965 RMVar_ID_53965 Human_SNP_ID_859459244 A-to-I Human chr5 - 34906413 34906413 34906413 GCTAATCTTGAACTCCTGAGCTCAAGCAATCCACCCGCCTCGGCCTCCCAAAGGGCTGGGATTAC GCTAATCTTGAACTCCTGAGCTCAAGCAATCCGCCCGCCTCGGCCTCCCAAAGGGCTGGGATTAC T C RAD1 Ensembl:ENSG00000113456 Protein coding 3'UTR GSE100210 HepG2 cell line chr5:34906412..34906413 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 53966 RMVar_ID_53966 Human_SNP_ID_859482566 A-to-I Human chr5 - 21883795 21883795 21883795 CAACATCACTTGTCCCACCAAACTTCAGCACAACTACTCCATCTGAAAGTTTTGCCAGCCATTCA CAACATCACTTGTCCCACCAAACTTCAGCACAGCTACTCCATCTGAAAGTTTTGCCAGCCATTCA T C CDH12 Ensembl:ENSG00000154162 Protein coding intron GSE100210 HepG2 cell line chr5:21883794..21883795 29129909 RNA-Seq:(High) rs1397783864 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue RMVar_hsa_circ_3898,RMVar_hsa_circ_334499 53967 RMVar_ID_53967 Human_SNP_ID_859509527 A-to-I Human chr5 - 74799412 74799412 74799412 GCCAATCCAAGCTGAGGACTGTGGAGCGAATCAGCTTTTTAATGTGCTTGCTCACCCACCAGTCA GCCAATCCAAGCTGAGGACTGTGGAGCGAATCGGCTTTTTAATGTGCTTGCTCACCCACCAGTCA T C FAM169A Ensembl:ENSG00000198780 Protein coding intron GSE100210 HepG2 cell line chr5:74799411..74799412 29129909 RNA-Seq:(High) rs1314100822 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue RMVar_hsa_circ_232496,RMVar_hsa_circ_268788,RMVar_hsa_circ_232493,RMVar_hsa_circ_232498,RMVar_hsa_circ_273983,RMVar_hsa_circ_310899,RMVar_hsa_circ_290453,RMVar_hsa_circ_271348,RMVar_hsa_circ_232497,RMVar_hsa_circ_232495 53968 RMVar_ID_53968 Human_SNP_ID_859541396 A-to-I Human chr5 + 128110773 128110773 128110773 TGCTAGAAAAACTTAAATGGACAAAAGATCACAATGAAGAGGCCAAAAAGATAGCAAAAGCAGGA TGCTAGAAAAACTTAAATGGACAAAAGATCACGATGAAGAGGCCAAAAAGATAGCAAAAGCAGGA A G SLC12A2,KDELC1P1 Ensembl:ENSG00000064651,Ensembl:ENSG00000250329 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line chr5:128110772..128110773 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue RMVar_hsa_circ_100540,RMVar_hsa_circ_234127 53969 RMVar_ID_53969 Human_SNP_ID_859547533 A-to-I Human chr5 + 157309800 157309800 157309800 GCGACATGCAGATAGAGCTGGCCAGATACATTAAGACCAGTGCTCACTATGAAGAGAACAAGTCC GCGACATGCAGATAGAGCTGGCCAGATACATTTAGACCAGTGCTCACTATGAAGAGAACAAGTCC A T CYFIP2 Ensembl:ENSG00000055163 Protein coding CDS GSE56152 embryonic stem cells,wild type chr5:157309799..157309800 25708366 RNA-Seq:(High) rs3207362 Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - Human_RBP_ID_1648993,Human_RBP_ID_1991157,Human_RBP_ID_18837131,Human_RBP_ID_19124909 Human_Splice_Rec_714462,Human_Splice_Rec_714463,Human_Splice_Rec_714512,Human_Splice_Rec_714513,Human_Splice_Rec_714564,Human_Splice_Rec_714565,Human_Splice_Rec_714622,Human_Splice_Rec_714623,Human_Splice_Rec_714688,Human_Splice_Rec_714689,Human_Splice_Rec_714798,Human_Splice_Rec_714799 RMVar_hsa_circ_1015,RMVar_hsa_circ_32668,RMVar_hsa_circ_310703,RMVar_hsa_circ_344306,RMVar_hsa_circ_49501,RMVar_hsa_circ_85272,RMVar_hsa_circ_31847,RMVar_hsa_circ_115477,RMVar_hsa_circ_105680,RMVar_hsa_circ_99611,RMVar_hsa_circ_101456,RMVar_hsa_circ_87019,RMVar_hsa_circ_235798,RMVar_hsa_circ_76709,RMVar_hsa_circ_22225,RMVar_hsa_circ_235800,RMVar_hsa_circ_235801,RMVar_hsa_circ_235799,RMVar_hsa_circ_235796,RMVar_hsa_circ_235797,RMVar_hsa_circ_235795,RMVar_hsa_circ_348540 53970 RMVar_ID_53970 Human_SNP_ID_859584692 A-to-I Human chr5 + 132351750 132351750 132351750 GCTAACAGAATACAGGCAAGAAACTGGATTCTACATATGTTGAAATTATGGCAAAAGACTTTATT GCTAACAGAATACAGGCAAGAAACTGGATTCTGCATATGTTGAAATTATGGCAAAAGACTTTATT A G lnc-SLC22A5-1 RNACentral:URS00008B5099 lincRNA intron GSE100210 HepG2 cell line chr5:132351749..132351750 29129909 RNA-Seq:(High) rs201881418 Functional Loss SNV ICGC 33..33 33 UTCA 1 - 53971 RMVar_ID_53971 Human_SNP_ID_859692581 A-to-I Human chr5 - 43380707 43380707 43380707 GCCTCAACTTCTAGGGCTCAAGCAATCCTCCCACCTCAGCCTCCCGAGTATCTGGGATCAAGGTG GCCTCAACTTCTAGGGCTCAAGCAATCCTCCCGCCTCAGCCTCCCGAGTATCTGGGATCAAGGTG T C CCL28 Ensembl:ENSG00000151882 Protein coding intron GSE38233 cultured B-cells chr5:43380706..43380707 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 53972 RMVar_ID_53972 Human_SNP_ID_859731190 A-to-I Human chr5 - 14846774 14846774 14846774 TTGGCCAGGCTGGGCTTGAACTCCTGATCCCAAGTAATCCATCCGCCTCAGCCTCCCAAAATATT TTGGCCAGGCTGGGCTTGAACTCCTGATCCCACGTAATCCATCCGCCTCAGCCTCCCAAAATATT T G ANKH Ensembl:ENSG00000154122 Protein coding intron GSE100210 HepG2 cell line chr5:14846773..14846774 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 53973 RMVar_ID_53973 Human_SNP_ID_859746106 A-to-I Human chr5 - 131162260 131162260 131162260 GGCTGCAGTGCAGTGGCACTCGGCTCACTGCAAGCTCCACCTCCCTGGTTCACACCATTCTCCTG GGCTGCAGTGCAGTGGCACTCGGCTCACTGCAGGCTCCACCTCCCTGGTTCACACCATTCTCCTG T C HINT1 Ensembl:ENSG00000169567 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line chr5:131162259..131162260 29129909,31158229 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue RMVar_hsa_circ_26252,RMVar_hsa_circ_64356 53974 RMVar_ID_53974 Human_SNP_ID_859800678 A-to-I Human chr5 + 21464397 21464397 21464397 GAGGCTGAGATGAGAGGGTCACTTGAGCCCAGAGGTTGAGGCTGCAGTGAGCTATGATCATGCCA GAGGCTGAGATGAGAGGGTCACTTGAGCCCAGCGGTTGAGGCTGCAGTGAGCTATGATCATGCCA A C GUSBP1 Ensembl:ENSG00000183666 Pseudogene intron GSE100210 HepG2 cell line chr5:21464396..21464397 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - RMVar_hsa_circ_46242,RMVar_hsa_circ_119679,RMVar_hsa_circ_230566,RMVar_hsa_circ_91454,RMVar_hsa_circ_230565 53975 RMVar_ID_53975 Human_SNP_ID_859826557 A-to-I Human chr5 - 108785137 108785137 108785137 ATGTGGTTGGTCTTCAGCTTGCAGTTAGCCAGATTCCATACCTTGACCAGCTTGTCCCAGCTACA ATGTGGTTGGTCTTCAGCTTGCAGTTAGCCAGGTTCCATACCTTGACCAGCTTGTCCCAGCTACA T C - - Other Unknown GSE100210 HepG2 cell line chr5:108785136..108785137 29129909 RNA-Seq:(High) rs560045904 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue 53976 RMVar_ID_53976 Human_SNP_ID_859845124 A-to-I Human chr5 - 115206724 115206724 115206724 TCTATAGATTTAGCATAAAGAAACATGCAAATAGGCAATGATACATTTTCAAGGATCTCACAGCC TCTATAGATTTAGCATAAAGAAACATGCAAATGGGCAATGATACATTTTCAAGGATCTCACAGCC T C PGGT1B Ensembl:ENSG00000164219 Protein coding 3'UTR GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line chr5:115206723..115206724 29129909,31158229,31158229,31158229 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 2 breast 53977 RMVar_ID_53977 Human_SNP_ID_859861332 A-to-I Human chr5 + 76242305 76242305 76242305 CCTTCAGCCTTTCTCTTGGGCATGGTGGCGGCAGCGACGGCAGCGGGACATAGGTGCTGGACGCG CCTTCAGCCTTTCTCTTGGGCATGGTGGCGGCGGCGACGGCAGCGGGACATAGGTGCTGGACGCG A G SV2C Ensembl:ENSG00000122012 Protein coding intron GSE100210 HepG2 cell line chr5:76242304..76242305 29129909 RNA-Seq:(High) rs878971128 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 53978 RMVar_ID_53978 Human_SNP_ID_859934055 A-to-I Human chr5 - 108785098 108785098 108785098 ACCTTGACCAGCTTGTCCCAGCTACAGGAGACAGTGATAGGGTTGCTGCTGTTAGGCAAGAAGCG ACCTTGACCAGCTTGTCCCAGCTACAGGAGACGGTGATAGGGTTGCTGCTGTTAGGCAAGAAGCG T C - - Other Unknown GSE100210 HepG2 cell line chr5:108785097..108785098 29129909 RNA-Seq:(High) rs879230548 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue 53979 RMVar_ID_53979 Human_SNP_ID_860084467 A-to-I Human chr5 - 146171959 146171959 146171959 GTTTGCTGTAGGGTACCAGCGATTGAAAGGAAAATGTTGTCTGTTTCCCTTTGGCCTGCACTGTA GTTTGCTGTAGGGTACCAGCGATTGAAAGGAACATGTTGTCTGTTTCCCTTTGGCCTGCACTGTA T G LARS1 Ensembl:ENSG00000133706 Protein coding intron GSE100210 HepG2 cell line chr5:146171958..146171959 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 endometrium endometrioid_carcinoma 4 uterus Human_RBP_ID_75327,Human_RBP_ID_214507,Human_RBP_ID_787903,Human_RBP_ID_943846,Human_RBP_ID_1647291,Human_RBP_ID_1989685,Human_RBP_ID_3968306,Human_RBP_ID_9262355,Human_RBP_ID_15339923,Human_RBP_ID_18835443,Human_RBP_ID_23051251,Human_RBP_ID_23214327,Human_RBP_ID_24089286,Human_RBP_ID_25868902 Human_Splice_Rec_704390,Human_Splice_Rec_704391,Human_Splice_Rec_704566,Human_Splice_Rec_704567,Human_Splice_Rec_704626,Human_Splice_Rec_704627,Human_Splice_Rec_704688,Human_Splice_Rec_704689,Human_Splice_Rec_704748,Human_Splice_Rec_704749,Human_Splice_Rec_704808,Human_Splice_Rec_704809,Human_Splice_Rec_704868,Human_Splice_Rec_704869,Human_Splice_Rec_704930,Human_Splice_Rec_704931,Human_Splice_Rec_704992,Human_Splice_Rec_704993,Human_Splice_Rec_705054,Human_Splice_Rec_705055,Human_Splice_Rec_705116,Human_Splice_Rec_705117,Human_Splice_Rec_705178,Human_Splice_Rec_705179,Human_Splice_Rec_705240,Human_Splice_Rec_705241,Human_Splice_Rec_705300,Human_Splice_Rec_705301,Human_Splice_Rec_705362,Human_Splice_Rec_705363,Human_Splice_Rec_705434,Human_Splice_Rec_705435,Human_Splice_Rec_705500,Human_Splice_Rec_705501,Human_Splice_Rec_705528,Human_Splice_Rec_705529,Human_Splice_Rec_705556,Human_Splice_Rec_705557,Human_Splice_Rec_705582,Human_Splice_Rec_705583,Human_Splice_Rec_705608,Human_Splice_Rec_705609,Human_Splice_Rec_705624,Human_Splice_Rec_705625 RMVar_hsa_circ_265072,RMVar_hsa_circ_100747,RMVar_hsa_circ_235236,RMVar_hsa_circ_45752,RMVar_hsa_circ_123626,RMVar_hsa_circ_235245,RMVar_hsa_circ_52850,RMVar_hsa_circ_19629,RMVar_hsa_circ_5318,RMVar_hsa_circ_235246,RMVar_hsa_circ_36119,RMVar_hsa_circ_113738,RMVar_hsa_circ_235251,RMVar_hsa_circ_321047,RMVar_hsa_circ_276318,RMVar_hsa_circ_235254,RMVar_hsa_circ_324107,RMVar_hsa_circ_235256,RMVar_hsa_circ_74803,RMVar_hsa_circ_235255,RMVar_hsa_circ_361066,RMVar_hsa_circ_274839,RMVar_hsa_circ_43830,RMVar_hsa_circ_343860,RMVar_hsa_circ_235257,RMVar_hsa_circ_307433,RMVar_hsa_circ_235258,RMVar_hsa_circ_235259,RMVar_hsa_circ_298505,RMVar_hsa_circ_337072 53980 RMVar_ID_53980 Human_SNP_ID_860084468 A-to-I Human chr5 - 146171959 146171959 146171959 GTTTGCTGTAGGGTACCAGCGATTGAAAGGAAAATGTTGTCTGTTTCCCTTTGGCCTGCACTGTA GTTTGCTGTAGGGTACCAGCGATTGAAAGGAAGATGTTGTCTGTTTCCCTTTGGCCTGCACTGTA T C LARS1 Ensembl:ENSG00000133706 Protein coding intron GSE100210 HepG2 cell line chr5:146171958..146171959 29129909 RNA-Seq:(High) rs112954500 Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_75327,Human_RBP_ID_214507,Human_RBP_ID_787903,Human_RBP_ID_943846,Human_RBP_ID_1647291,Human_RBP_ID_1989685,Human_RBP_ID_3968306,Human_RBP_ID_9262355,Human_RBP_ID_15339923,Human_RBP_ID_18835443,Human_RBP_ID_23051251,Human_RBP_ID_23214327,Human_RBP_ID_24089286,Human_RBP_ID_25868902 Human_Splice_Rec_704390,Human_Splice_Rec_704391,Human_Splice_Rec_704566,Human_Splice_Rec_704567,Human_Splice_Rec_704626,Human_Splice_Rec_704627,Human_Splice_Rec_704688,Human_Splice_Rec_704689,Human_Splice_Rec_704748,Human_Splice_Rec_704749,Human_Splice_Rec_704808,Human_Splice_Rec_704809,Human_Splice_Rec_704868,Human_Splice_Rec_704869,Human_Splice_Rec_704930,Human_Splice_Rec_704931,Human_Splice_Rec_704992,Human_Splice_Rec_704993,Human_Splice_Rec_705054,Human_Splice_Rec_705055,Human_Splice_Rec_705116,Human_Splice_Rec_705117,Human_Splice_Rec_705178,Human_Splice_Rec_705179,Human_Splice_Rec_705240,Human_Splice_Rec_705241,Human_Splice_Rec_705300,Human_Splice_Rec_705301,Human_Splice_Rec_705362,Human_Splice_Rec_705363,Human_Splice_Rec_705434,Human_Splice_Rec_705435,Human_Splice_Rec_705500,Human_Splice_Rec_705501,Human_Splice_Rec_705528,Human_Splice_Rec_705529,Human_Splice_Rec_705556,Human_Splice_Rec_705557,Human_Splice_Rec_705582,Human_Splice_Rec_705583,Human_Splice_Rec_705608,Human_Splice_Rec_705609,Human_Splice_Rec_705624,Human_Splice_Rec_705625 Clinvar_Rec_142 RMVar_hsa_circ_265072,RMVar_hsa_circ_100747,RMVar_hsa_circ_235236,RMVar_hsa_circ_45752,RMVar_hsa_circ_123626,RMVar_hsa_circ_235245,RMVar_hsa_circ_52850,RMVar_hsa_circ_19629,RMVar_hsa_circ_5318,RMVar_hsa_circ_235246,RMVar_hsa_circ_36119,RMVar_hsa_circ_113738,RMVar_hsa_circ_235251,RMVar_hsa_circ_321047,RMVar_hsa_circ_276318,RMVar_hsa_circ_235254,RMVar_hsa_circ_324107,RMVar_hsa_circ_235256,RMVar_hsa_circ_74803,RMVar_hsa_circ_235255,RMVar_hsa_circ_361066,RMVar_hsa_circ_274839,RMVar_hsa_circ_43830,RMVar_hsa_circ_343860,RMVar_hsa_circ_235257,RMVar_hsa_circ_307433,RMVar_hsa_circ_235258,RMVar_hsa_circ_235259,RMVar_hsa_circ_298505,RMVar_hsa_circ_337072 53981 RMVar_ID_53981 Human_SNP_ID_860100576 A-to-I Human chr5 - 60605837 60605837 60605837 TTTTCTAAATCAGGTTTGTTACAGAAGGAGAAAGTGGCAGTTGAAGCATTTCAGATTTGCTGCCT TTTTCTAAATCAGGTTTGTTACAGAAGGAGAAGGTGGCAGTTGAAGCATTTCAGATTTGCTGCCT T C DEPDC1B Ensembl:ENSG00000035499 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector chr5:60605836..60605837 29967493 RNA-Seq:(High) - Functional Loss SNV TCGA 33..33 33 GBM 1 - Human_Splice_Rec_654082,Human_Splice_Rec_654102,Human_Splice_Rec_654122,Human_Splice_Rec_654128 Human_miRNA_ID_1379576 RMVar_hsa_circ_1770,RMVar_hsa_circ_124285,RMVar_hsa_circ_231609,RMVar_hsa_circ_231608,RMVar_hsa_circ_305097,RMVar_hsa_circ_358689,RMVar_hsa_circ_40647,RMVar_hsa_circ_231610,RMVar_hsa_circ_108526 53982 RMVar_ID_53982 Human_SNP_ID_860105041 A-to-I Human chr5 + 173929535 173929535 173929535 AGCCTGGGTAACATAGGGAGACCCCCATCTCTACATAAAATAAAAAATTAGCCAGGCATGGTGGC AGCCTGGGTAACATAGGGAGACCCCCATCTCTGCATAAAATAAAAAATTAGCCAGGCATGGTGGC A G CPEB4 Ensembl:ENSG00000113742 Protein coding intron GSE100210 HepG2 cell line chr5:173929534..173929535 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_71257,RMVar_hsa_circ_236297,RMVar_hsa_circ_103933,RMVar_hsa_circ_311433,RMVar_hsa_circ_334639,RMVar_hsa_circ_236299,RMVar_hsa_circ_38068,RMVar_hsa_circ_236300 53983 RMVar_ID_53983 Human_SNP_ID_860107602 A-to-I Human chr5 + 75592935 75592935 75592935 AAAATTAGCTGGGCATGGTGGCACGAGTGTGTAGTCCCAGCTACTTGGGAGGCTGAGGTAGGAGG AAAATTAGCTGGGCATGGTGGCACGAGTGTGTGGTCCCAGCTACTTGGGAGGCTGAGGTAGGAGG A G POLK Ensembl:ENSG00000122008 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line chr5:75592934..75592935 31158229 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_9090,RMVar_hsa_circ_40894,RMVar_hsa_circ_232559,RMVar_hsa_circ_29797,RMVar_hsa_circ_14023 53984 RMVar_ID_53984 Human_SNP_ID_860169674 A-to-I Human chr5 + 34819800 34819800 34819800 TATTTATTGATTTATTTTAGAGATGGGGTCTTACTGTATTGCCCAGACTGGTCTCAAACTCCTGA TATTTATTGATTTATTTTAGAGATGGGGTCTTCCTGTATTGCCCAGACTGGTCTCAAACTCCTGA A C RAI14 Ensembl:ENSG00000039560 Protein coding intron GSE100210 HepG2 cell line chr5:34819799..34819800 29129909 RNA-Seq:(High) rs1032858600 Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_32419,RMVar_hsa_circ_84569,RMVar_hsa_circ_127467,RMVar_hsa_circ_230766,RMVar_hsa_circ_230767,RMVar_hsa_circ_323304,RMVar_hsa_circ_368664,RMVar_hsa_circ_68994,RMVar_hsa_circ_230774,RMVar_hsa_circ_230773,RMVar_hsa_circ_336330,RMVar_hsa_circ_307835,RMVar_hsa_circ_353874,RMVar_hsa_circ_306930,RMVar_hsa_circ_230777,RMVar_hsa_circ_230778,RMVar_hsa_circ_314788,RMVar_hsa_circ_230780,RMVar_hsa_circ_356022,RMVar_hsa_circ_230779,RMVar_hsa_circ_367804,RMVar_hsa_circ_316953 53985 RMVar_ID_53985 Human_SNP_ID_860227880 A-to-I Human chr5 - 115838991 115838991 115838991 AGCCTCCCAAGTAGCTGAGATTACGGGCATGCACCACCACGCCTGGCTAAGTTTTTGTATTTTTA AGCCTCCCAAGTAGCTGAGATTACGGGCATGCGCCACCACGCCTGGCTAAGTTTTTGTATTTTTA T C ATG12 Ensembl:ENSG00000145782 Protein coding intron GSE38233 cultured B-cells chr5:115838990..115838991 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - 53986 RMVar_ID_53986 Human_SNP_ID_860287941 A-to-I Human chr5 + 132644904 132644904 132644904 GCAATCCTCCTGCCTCAGCCTCCCAAGTAGCTAGGATTACAGGCATGTACCACCACACCAGGCTA GCAATCCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCATGTACCACCACACCAGGCTA A G AC116366.3,RAD50 Ensembl:ENSG00000283782,Ensembl:ENSG00000113522 Protein coding,Protein coding 3'UTR,3'UTR GSE38233 cultured B-cells chr5:132644903..132644904 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 53987 RMVar_ID_53987 Human_SNP_ID_860306718 A-to-I Human chr5 + 154845497 154845463 154845498 GGAAGTTGGACTGGGCATGGTGTCTCATGCCTATCATCCCAGCACTTTGAGAGGCTGAAGCGGGA __________________________________CATCCCAGCACTTTGAGAGGCTGAAGCGGGA CTGGAAGTTGGACTGGGCATGGTGTCTCATGCCTAT C - - Other Unknown GSE100210 HepG2 cell line chr5:154845496..154845497 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 1..34 33 LICA 1 - 53988 RMVar_ID_53988 Human_SNP_ID_860326109 A-to-I Human chr5 - 140684238 140684238 140684238 TCTCCCAGGCTGGAGTGCAGTGGCACTATCTCAGCTCACTGCAAGCTCCACCTGCCGGGTTCACG TCTCCCAGGCTGGAGTGCAGTGGCACTATCTCGGCTCACTGCAAGCTCCACCTGCCGGGTTCACG T C HARS1 Ensembl:ENSG00000170445 Protein coding intron GSE38233 cultured B-cells chr5:140684237..140684238 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 9 oesophagus RMVar_hsa_circ_90848,RMVar_hsa_circ_235049 53989 RMVar_ID_53989 Human_SNP_ID_860466219 A-to-I Human chr5 + 134850691 134850691 134850691 TAGAGACGGGGTTTTACCATTTTGGCCAGGCTAGTCTCAAACTCCTGACCTCAGGTGATCTGCCT TAGAGACGGGGTTTTACCATTTTGGCCAGGCTGGTCTCAAACTCCTGACCTCAGGTGATCTGCCT A G DDX46,C5orf24 Ensembl:ENSG00000145833,Ensembl:ENSG00000181904 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells chr5:134850690..134850691 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 CMDI 1 - RMVar_hsa_circ_107835,RMVar_hsa_circ_110532,RMVar_hsa_circ_234623,RMVar_hsa_circ_234624 53990 RMVar_ID_53990 Human_SNP_ID_860484073 A-to-I Human chr5 - 177529202 177529202 177529202 TGTCTACACGAAGGTGAGAGAGTCATGGGCTGACAGTGGGAGAAGGGAGCAGAGAGACACCCTGC TGTCTACACGAAGGTGAGAGAGTCATGGGCTGGCAGTGGGAGAAGGGAGCAGAGAGACACCCTGC T C FAM193B Ensembl:ENSG00000146067 Protein coding intron GSE100210 HepG2 cell line chr5:177529201..177529202 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - RMVar_hsa_circ_14756,RMVar_hsa_circ_77947,RMVar_hsa_circ_236538 53991 RMVar_ID_53991 Human_SNP_ID_860587552 A-to-I Human chr5 - 59423312 59423312 59423312 AAATATGTGATTACAATTGTGAGAACTGCTCAAAAGGAAACAAGGACCCAGTGAGAGTATAAAAA AAATATGTGATTACAATTGTGAGAACTGCTCACAAGGAAACAAGGACCCAGTGAGAGTATAAAAA T G PDE4D Ensembl:ENSG00000113448 Protein coding intron GSE100210 HepG2 cell line chr5:59423311..59423312 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 7 prostate RMVar_hsa_circ_25249,RMVar_hsa_circ_7785,RMVar_hsa_circ_26973,RMVar_hsa_circ_231584,RMVar_hsa_circ_231590,RMVar_hsa_circ_231585,RMVar_hsa_circ_231587,RMVar_hsa_circ_231586 53992 RMVar_ID_53992 Human_SNP_ID_860622299 A-to-I Human chr5 - 151111645 151111645 151111645 GGTCAAGGTTGCAGTGAGCCGAGATTGTGCCAATGTACTCCAGCCTGGGCAACAGAGCAAGACCC GGTCAAGGTTGCAGTGAGCCGAGATTGTGCCAGTGTACTCCAGCCTGGGCAACAGAGCAAGACCC T C ANXA6 Ensembl:ENSG00000197043 Protein coding intron GSE38233 cultured B-cells chr5:151111644..151111645 24183664 RNA-Seq:(High) rs550908766 Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_17307,RMVar_hsa_circ_14800,RMVar_hsa_circ_49486,RMVar_hsa_circ_79861,RMVar_hsa_circ_87688,RMVar_hsa_circ_69720,RMVar_hsa_circ_102842,RMVar_hsa_circ_123405,RMVar_hsa_circ_235533,RMVar_hsa_circ_235534,RMVar_hsa_circ_320895,RMVar_hsa_circ_128126,RMVar_hsa_circ_110844,RMVar_hsa_circ_235538,RMVar_hsa_circ_235540,RMVar_hsa_circ_235539,RMVar_hsa_circ_235537,RMVar_hsa_circ_65293,RMVar_hsa_circ_288331,RMVar_hsa_circ_102581,RMVar_hsa_circ_235541 53993 RMVar_ID_53993 Human_SNP_ID_860630213 A-to-I Human chr5 - 137879076 137879076 137879076 TACAAAAACTAGCCAGCACGGTGTGCGCACCTATAGTCCCATCTATTTGGGAGTCTGAGGCACGA TACAAAAACTAGCCAGCACGGTGTGCGCACCTGTAGTCCCATCTATTTGGGAGTCTGAGGCACGA T C AC106791.1 Ensembl:ENSG00000250159 lincRNA intron GSE100210 HepG2 cell line chr5:137879075..137879076 29129909 RNA-Seq:(High) rs1384309398 Functional Loss SNV ICGC 33..33 33 MALY 1 - 53994 RMVar_ID_53994 Human_SNP_ID_860705479 A-to-I Human chr5 - 151746431 151746431 151746431 TCCTCTTCCTGCAGGAGTTAAGTATGACATTGACCTGCCCAACAAGAAGGTCTGCATTGAATCTG TCCTCTTCCTGCAGGAGTTAAGTATGACATTGGCCTGCCCAACAAGAAGGTCTGCATTGAATCTG T C ATOX1 Ensembl:ENSG00000177556 Protein coding CDS GSE100210 HepG2 cell line chr5:151746430..151746431 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA 33..33 33 OV 1 - Human_RBP_ID_635572,Human_RBP_ID_1648443,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 53995 RMVar_ID_53995 Human_SNP_ID_860784157 A-to-I Human chr5 - 25910227 25910227 25910227 TTGAAAGAAATGCTCCTGATTTCACTCCAAGGAAAGCCTATCTTGGGAGTTAGTCTGTCATGCTG TTGAAAGAAATGCTCCTGATTTCACTCCAAGGGAAGCCTATCTTGGGAGTTAGTCTGTCATGCTG T C - - Other Unknown GSE100210 HepG2 cell line chr5:25910226..25910227 29129909 RNA-Seq:(High) rs1169825342 Functional Loss SNV ICGC 33..33 33 LAML 1 - 53996 RMVar_ID_53996 Human_SNP_ID_860796018 A-to-I Human chr5 + 97031897 97031896 97031897 ACAAAGCGAGACTGTCTCAAAAAACAAAAAACAAAAAAAAAAGAGTTAAGTGTTGATTTTGTTGG ACAAAGCGAGACTGTCTCAAAAAACAAAAAAC_AAAAAAAAAGAGTTAAGTGTTGATTTTGTTGG CA C LNPEP Ensembl:ENSG00000113441 Protein coding 3'UTR GSE100210 HepG2 cell line chr5:97031896..97031897 29129909 RNA-Seq:(High) rs149987000 Functional Loss DEL ICGC 33..33 33 COCA 1 - 53997 RMVar_ID_53997 Human_SNP_ID_860827304 A-to-I Human chr5 - 54076297 54076297 54076297 CCTGCCTCAGCCTCCCGAATACCTGGAACTACAGGCGCCTGCCACCATGCACAGCTAATTTTTTT CCTGCCTCAGCCTCCCGAATACCTGGAACTACGGGCGCCTGCCACCATGCACAGCTAATTTTTTT T C ARL15 Ensembl:ENSG00000185305 Protein coding intron GSE100210 HepG2 cell line chr5:54076296..54076297 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_114374,RMVar_hsa_circ_231366 53998 RMVar_ID_53998 Human_SNP_ID_860870314 A-to-I Human chr5 - 94143327 94143327 94143327 AATGAAATCTTGTCAATTGCATCAACATGGATAGAACTGGAAATTTTGTGTTAAGTGGAATAAGA AATGAAATCTTGTCAATTGCATCAACATGGATTGAACTGGAAATTTTGTGTTAAGTGGAATAAGA T A - - Other Unknown GSE100210 HepG2 cell line chr5:94143326..94143327 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 53999 RMVar_ID_53999 Human_SNP_ID_860931281 A-to-I Human chr5 - 132203838 132203838 132203838 TCTGCCCTTTTCTTTTTGCCCAGCTCCTGGCTAGAGGAAGATGATGACCCTGTTGTGGCCCGAGT TCTGCCCTTTTCTTTTTGCCCAGCTCCTGGCTGGAGGAAGATGATGACCCTGTTGTGGCCCGAGT T C P4HA2 Ensembl:ENSG00000072682 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector chr5:132203837..132203838 29967493 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 lung squamous_cell_carcinoma 6 lung Human_RBP_ID_942938,Human_RBP_ID_3968126,Human_RBP_ID_4807606,Human_RBP_ID_22771730 Human_Splice_Rec_690076,Human_Splice_Rec_690077,Human_Splice_Rec_690106,Human_Splice_Rec_690107,Human_Splice_Rec_690136,Human_Splice_Rec_690137,Human_Splice_Rec_690164,Human_Splice_Rec_690165,Human_Splice_Rec_690192,Human_Splice_Rec_690193,Human_Splice_Rec_690220,Human_Splice_Rec_690221 RMVar_hsa_circ_2731,RMVar_hsa_circ_84873,RMVar_hsa_circ_234336,RMVar_hsa_circ_234337,RMVar_hsa_circ_36522,RMVar_hsa_circ_315077 54000 RMVar_ID_54000 Human_SNP_ID_860942814 A-to-I Human chr5 - 14741844 14741844 14741844 CAGCCCACATCAAGAAGTTCACCTTCGTCTGCATGGCTCTGTCACTCACGGTAAGGACAGAGGCT CAGCCCACATCAAGAAGTTCACCTTCGTCTGCGTGGCTCTGTCACTCACGGTAAGGACAGAGGCT T C ANKH Ensembl:ENSG00000154122 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector chr5:14741843..14741844 29967493 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_8886186 Human_Splice_Rec_636692,Human_Splice_Rec_636693,Human_Splice_Rec_636714,Human_Splice_Rec_636715,Human_Splice_Rec_636720 RMVar_hsa_circ_91481,RMVar_hsa_circ_122705,RMVar_hsa_circ_266209,RMVar_hsa_circ_230466,RMVar_hsa_circ_230463,RMVar_hsa_circ_279780,RMVar_hsa_circ_339274,RMVar_hsa_circ_345724,RMVar_hsa_circ_230467,RMVar_hsa_circ_277143,RMVar_hsa_circ_354171,RMVar_hsa_circ_230465,RMVar_hsa_circ_299003,RMVar_hsa_circ_270437,RMVar_hsa_circ_230468,RMVar_hsa_circ_230470,RMVar_hsa_circ_230471,RMVar_hsa_circ_230472,RMVar_hsa_circ_230469 54001 RMVar_ID_54001 Human_SNP_ID_860956312 A-to-I Human chr5 - 179677109 179677101 179677110 GGTCAGGAGTTAAAAGGCCATCCTGACCAACAAGGTGAAACCATGTCTCTACTAAAAATACCAAA GGTCAGGAGTTAAAAGGCCATCCTGACCAAC_________CCATGTCTCTACTAAAAATACCAAA GTTTCACCTT G lnc-CBY3-1 RNACentral:URS0000D5B916 lincRNA intron GSE100210 HepG2 cell line chr5:179677108..179677109 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 32..40 33 PAAD 1 - Human_RBP_ID_23193209 54002 RMVar_ID_54002 Human_SNP_ID_860958370 A-to-I Human chr5 + 72906457 72906456 72906457 GGCATTACAGGCACATGCCACCATGCCTGGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCA GGCATTACAGGCACATGCCACCATGCCTGGCT_ATTTTTGTATTTTTAGTAGAGATGGGGTTTCA TA T TNPO1 Ensembl:ENSG00000083312 Protein coding intron GSE38233 cultured B-cells chr5:72906456..72906457 24183664 RNA-Seq:(High) - Functional Loss DEL ICGC 33..33 33 PBCA 1 - 54003 RMVar_ID_54003 Human_SNP_ID_860965867 A-to-I Human chr5 - 37208528 37208528 37208528 GGACTACAGGCGCCCACCACCTCGCTGGGCTAATTTTTTGTATTTTTAGTGGAGACGGGGTTTCA GGACTACAGGCGCCCACCACCTCGCTGGGCTATTTTTTTGTATTTTTAGTGGAGACGGGGTTTCA T A CPLANE1 Ensembl:ENSG00000197603 Protein coding intron GSE100210 HepG2 cell line chr5:37208527..37208528 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_313599,RMVar_hsa_circ_37191,RMVar_hsa_circ_19407,RMVar_hsa_circ_36271,RMVar_hsa_circ_25842,RMVar_hsa_circ_230922,RMVar_hsa_circ_86106,RMVar_hsa_circ_230924,RMVar_hsa_circ_230925,RMVar_hsa_circ_38346,RMVar_hsa_circ_36226,RMVar_hsa_circ_304351,RMVar_hsa_circ_265172,RMVar_hsa_circ_28047,RMVar_hsa_circ_26337,RMVar_hsa_circ_230927,RMVar_hsa_circ_319381,RMVar_hsa_circ_230937,RMVar_hsa_circ_298314,RMVar_hsa_circ_284218,RMVar_hsa_circ_230943,RMVar_hsa_circ_12287,RMVar_hsa_circ_230941,RMVar_hsa_circ_230942,RMVar_hsa_circ_230940,RMVar_hsa_circ_40657,RMVar_hsa_circ_338561,RMVar_hsa_circ_292326,RMVar_hsa_circ_49570,RMVar_hsa_circ_230944,RMVar_hsa_circ_25476,RMVar_hsa_circ_285666,RMVar_hsa_circ_294837,RMVar_hsa_circ_72202,RMVar_hsa_circ_230949,RMVar_hsa_circ_230947,RMVar_hsa_circ_230948,RMVar_hsa_circ_345181,RMVar_hsa_circ_368892,RMVar_hsa_circ_49138,RMVar_hsa_circ_358673,RMVar_hsa_circ_14931,RMVar_hsa_circ_25205,RMVar_hsa_circ_7419,RMVar_hsa_circ_334456,RMVar_hsa_circ_230951,RMVar_hsa_circ_334936,RMVar_hsa_circ_299392,RMVar_hsa_circ_329552,RMVar_hsa_circ_9439,RMVar_hsa_circ_230952,RMVar_hsa_circ_230954,RMVar_hsa_circ_230955,RMVar_hsa_circ_230953,RMVar_hsa_circ_71306 54004 RMVar_ID_54004 Human_SNP_ID_860972755 A-to-I Human chr5 - 132922387 132922387 132922387 CTTTTTAAGACAAGGTCTCTGTTGTCCAGGCTAGAGTGCAGTGGCATGATCATGGCTCATTGCAC CTTTTTAAGACAAGGTCTCTGTTGTCCAGGCTGGAGTGCAGTGGCATGATCATGGCTCATTGCAC T C AFF4 Ensembl:ENSG00000072364 Protein coding intron GSE100210 HepG2 cell line chr5:132922386..132922387 29129909 RNA-Seq:(High) rs1404868862 Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_15558524,Human_RBP_ID_17575306 RMVar_hsa_circ_99039,RMVar_hsa_circ_234392,RMVar_hsa_circ_60074,RMVar_hsa_circ_80330,RMVar_hsa_circ_234399,RMVar_hsa_circ_268115,RMVar_hsa_circ_70765,RMVar_hsa_circ_268451,RMVar_hsa_circ_29131,RMVar_hsa_circ_69535,RMVar_hsa_circ_70682 54005 RMVar_ID_54005 Human_SNP_ID_860974742 A-to-I Human chr5 - 59378391 59378391 59378391 AGTTCAGGGGTACATGTGCAGGTTTGTTATATAGGTAAACTTGGGTCACAGGGGCTTCTTGTACA AGTTCAGGGGTACATGTGCAGGTTTGTTATATGGGTAAACTTGGGTCACAGGGGCTTCTTGTACA T C PDE4D Ensembl:ENSG00000113448 Protein coding intron GSE107867 ASD brains,temporal_cortex chr5:59378390..59378391 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_25249,RMVar_hsa_circ_7785,RMVar_hsa_circ_26973 54006 RMVar_ID_54006 Human_SNP_ID_860975613 A-to-I Human chr5 - 17203379 17203379 17203379 GCTCTGCCGCCAGGCTGGACTGAAGTGGCGCAATCTCGGCTCACTGAAACCTCTGCCTCCTGGGT GCTCTGCCGCCAGGCTGGACTGAAGTGGCGCATTCTCGGCTCACTGAAACCTCTGCCTCCTGGGT T A BASP1-AS1 Ensembl:ENSG00000215196 lincRNA intron GSE100210 HepG2 cell line chr5:17203378..17203379 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 54007 RMVar_ID_54007 Human_SNP_ID_861090894 A-to-I Human chr5 - 107725323 107725323 107725323 TTGTCATCTTCTATAAATCCTTTCTCAGGATCAGTCACTTCACTCCAGGCCATAAAATTGGAAAA TTGTCATCTTCTATAAATCCTTTCTCAGGATCGGTCACTTCACTCCAGGCCATAAAATTGGAAAA T C - - Other Unknown GSE100210 HepG2 cell line chr5:107725322..107725323 29129909 RNA-Seq:(High) rs1341608495 Functional Loss SNV ICGC 33..33 33 LAML 2 - 54008 RMVar_ID_54008 Human_SNP_ID_861115635 A-to-I Human chr5 + 126625741 126625741 126625741 GGGGGGTTTTTTAGTTAGAGTCTTGATCTGTCACCCAGGCTGGAGTACAGTGGCAGGATCTCAGC GGGGGGTTTTTTAGTTAGAGTCTTGATCTGTCGCCCAGGCTGGAGTACAGTGGCAGGATCTCAGC A G PHAX Ensembl:ENSG00000164902 Protein coding 3'UTR GSE100210 HepG2 cell line chr5:126625740..126625741 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_629985 RMVar_hsa_circ_80867,RMVar_hsa_circ_234086,RMVar_hsa_circ_113766,RMVar_hsa_circ_234090 54009 RMVar_ID_54009 Human_SNP_ID_861147238 A-to-I Human chr5 + 1812906 1812906 1812906 GAAACCCTGTCTCTACTAAAAATACAAAAATTAGTCGGACGTGGTGGCGGGTGCCTGTAATCCCA GAAACCCTGTCTCTACTAAAAATACAAAAATTGGTCGGACGTGGTGGCGGGTGCCTGTAATCCCA A G NDUFS6 Ensembl:ENSG00000145494 Protein coding intron GSE100210 HepG2 cell line chr5:1812905..1812906 29129909 RNA-Seq:(High) rs767308501 Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_81273,RMVar_hsa_circ_100999,RMVar_hsa_circ_230062,RMVar_hsa_circ_230063 54010 RMVar_ID_54010 Human_SNP_ID_861167350 A-to-I Human chr5 + 172937527 172937527 172937527 CTCCCTACAAAAGAAAAGTTAAAAAATTAGCTAGACATAGTGGTGCATGCCTGTAGTTTCAGCTA CTCCCTACAAAAGAAAAGTTAAAAAATTAGCTTGACATAGTGGTGCATGCCTGTAGTTTCAGCTA A T ERGIC1 Ensembl:ENSG00000113719 Protein coding intron GSE100210 HepG2 cell line chr5:172937526..172937527 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 54011 RMVar_ID_54011 Human_SNP_ID_861167610 A-to-I Human chr5 - 77785099 77785099 77785099 ATGTCGTCCCAGTTGGTGACAATGCCGTGCTCAATGGGGTACTTCAGGGTGAGGATGCCTCTCTT ATGTCGTCCCAGTTGGTGACAATGCCGTGCTCGATGGGGTACTTCAGGGTGAGGATGCCTCTCTT T C TBCA Ensembl:ENSG00000171530 Protein coding intron GSE100210 HepG2 cell line chr5:77785098..77785099 29129909 RNA-Seq:(High) rs879222952 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue 54012 RMVar_ID_54012 Human_SNP_ID_861307934 A-to-I Human chr5 + 176308267 176308267 176308267 AAATGCGCACAGTTGCTGAAAAGGTTGATGCCATCAGAATTGTTCACATTCGTTCTGTCATCATC AAATGCGCACAGTTGCTGAAAAGGTTGATGCCGTCAGAATTGTTCACATTCGTTCTGTCATCATC A G BRCC3P1,SIMC1 Ensembl:ENSG00000251667,Ensembl:ENSG00000170085 Pseudogene,Protein coding exon,intron GSE38233 cultured B-cells chr5:176308266..176308267 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 10 haematopoietic and lymphoid tissue Human_RBP_ID_9183389 RMVar_hsa_circ_58004,RMVar_hsa_circ_63765,RMVar_hsa_circ_306548,RMVar_hsa_circ_309390,RMVar_hsa_circ_236342,RMVar_hsa_circ_322535 54013 RMVar_ID_54013 Human_SNP_ID_861318909 A-to-I Human chr5 + 178144637 178144637 178144637 GGCGTTTGTAGTCCCAGCTACTAGGCTGAAGCAGGAGAATGGCATGAACCCGGGAGGCGGAGCTT GGCGTTTGTAGTCCCAGCTACTAGGCTGAAGCCGGAGAATGGCATGAACCCGGGAGGCGGAGCTT A C RMND5B Ensembl:ENSG00000145916 Protein coding intron GSE100210 HepG2 cell line chr5:178144636..178144637 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast HER-positive_carcinoma 4 breast 54014 RMVar_ID_54014 Human_SNP_ID_861342653 A-to-I Human chr5 + 55374413 55374413 55374413 GGGCTCAAGGAATCCTCCAACCTCAGCCTCCCAAGTAGCTAGGACCACAGGTGTGTACCATCACA GGGCTCAAGGAATCCTCCAACCTCAGCCTCCCTAGTAGCTAGGACCACAGGTGTGTACCATCACA A T MTREX Ensembl:ENSG00000039123 Protein coding intron GSE100210 HepG2 cell line chr5:55374412..55374413 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 2 breast 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_10290,RMVar_hsa_circ_306042,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_297257,RMVar_hsa_circ_231415,RMVar_hsa_circ_231416,RMVar_hsa_circ_231426,RMVar_hsa_circ_27044,RMVar_hsa_circ_286698,RMVar_hsa_circ_126461,RMVar_hsa_circ_121598,RMVar_hsa_circ_231428,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_338978,RMVar_hsa_circ_60619,RMVar_hsa_circ_37695,RMVar_hsa_circ_231440,RMVar_hsa_circ_297755,RMVar_hsa_circ_286436,RMVar_hsa_circ_351013,RMVar_hsa_circ_67412,RMVar_hsa_circ_231441 54015 RMVar_ID_54015 Human_SNP_ID_861346231 A-to-I Human chr5 + 94681111 94681110 94681112 AGGCTTCAAATTCGGTTATAGCTAGGCAGTTTAAAAGTTTTAAACATTATTTCTTTTGTCTTTTT AGGCTTCAAATTCGGTTATAGCTAGGCAGTTT__AAGTTTTAAACATTATTTCTTTTGTCTTTTT TAA T SLF1 Ensembl:ENSG00000133302 Protein coding intron GSE100210 HepG2 cell line chr5:94681110..94681111 29129909 RNA-Seq:(High) rs965484410 Functional Loss DEL ICGC 33..34 33 PBCA 1 - RMVar_hsa_circ_341114,RMVar_hsa_circ_45913,RMVar_hsa_circ_102015,RMVar_hsa_circ_233292,RMVar_hsa_circ_2443,RMVar_hsa_circ_33951,RMVar_hsa_circ_304218 54016 RMVar_ID_54016 Human_SNP_ID_861487774 A-to-I Human chr5 - 82276072 82276072 82276072 TAATGGTGAAAACACTGTAGTAATAAATTTTCATATGCCAAAAAATGTTTGTATCTTACTGTCCC TAATGGTGAAAACACTGTAGTAATAAATTTTCGTATGCCAAAAAATGTTTGTATCTTACTGTCCC T C RPS23 Ensembl:ENSG00000186468 Protein coding 3'UTR GSE38233 cultured B-cells chr5:82276071..82276072 24183664 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 central_nervous_system medullomyoblastoma,brain medullomyoblastoma 5 brain Human_RBP_ID_647691,Human_RBP_ID_1213870,Human_RBP_ID_1658891,Human_RBP_ID_2000790,Human_RBP_ID_2947924,Human_RBP_ID_3779577,Human_RBP_ID_5212820,Human_RBP_ID_8623384,Human_RBP_ID_15535337,Human_RBP_ID_17197534,Human_RBP_ID_17662312,Human_RBP_ID_18054506,Human_RBP_ID_18362010,Human_RBP_ID_18449162,Human_RBP_ID_18848192,Human_RBP_ID_21901184,Human_RBP_ID_22303226,Human_RBP_ID_22828887,Human_RBP_ID_23048350,Human_RBP_ID_24508425,Human_RBP_ID_25923840,Human_RBP_ID_26528550,Human_RBP_ID_26706223,Human_RBP_ID_27084754,Human_RBP_ID_27338710,Human_RBP_ID_27517570,Human_RBP_ID_27744907 RMVar_hsa_circ_123992,RMVar_hsa_circ_23344,RMVar_hsa_circ_232949 54017 RMVar_ID_54017 Human_SNP_ID_861496585 A-to-I Human chr5 - 37209476 37209476 37209476 TTAACTCATGAATTAGCTGGTTTCGAAGTTGTATCTTGAGTGTTTCCAGTATACCCCGATCCTTA TTAACTCATGAATTAGCTGGTTTCGAAGTTGTGTCTTGAGTGTTTCCAGTATACCCCGATCCTTA T C CPLANE1 Ensembl:ENSG00000197603 Protein coding intron GSE100210 HepG2 cell line chr5:37209475..37209476 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue Human_RBP_ID_2929894 RMVar_hsa_circ_313599,RMVar_hsa_circ_37191,RMVar_hsa_circ_19407,RMVar_hsa_circ_36271,RMVar_hsa_circ_25842,RMVar_hsa_circ_230922,RMVar_hsa_circ_86106,RMVar_hsa_circ_230924,RMVar_hsa_circ_230925,RMVar_hsa_circ_38346,RMVar_hsa_circ_36226,RMVar_hsa_circ_304351,RMVar_hsa_circ_265172,RMVar_hsa_circ_28047,RMVar_hsa_circ_26337,RMVar_hsa_circ_230927,RMVar_hsa_circ_319381,RMVar_hsa_circ_230937,RMVar_hsa_circ_298314,RMVar_hsa_circ_284218,RMVar_hsa_circ_230943,RMVar_hsa_circ_12287,RMVar_hsa_circ_230941,RMVar_hsa_circ_230942,RMVar_hsa_circ_230940,RMVar_hsa_circ_40657,RMVar_hsa_circ_338561,RMVar_hsa_circ_292326,RMVar_hsa_circ_49570,RMVar_hsa_circ_230944,RMVar_hsa_circ_25476,RMVar_hsa_circ_285666,RMVar_hsa_circ_294837,RMVar_hsa_circ_72202,RMVar_hsa_circ_230949,RMVar_hsa_circ_230947,RMVar_hsa_circ_230948,RMVar_hsa_circ_345181,RMVar_hsa_circ_368892,RMVar_hsa_circ_49138,RMVar_hsa_circ_358673,RMVar_hsa_circ_14931,RMVar_hsa_circ_25205,RMVar_hsa_circ_7419,RMVar_hsa_circ_334456,RMVar_hsa_circ_230951,RMVar_hsa_circ_334936,RMVar_hsa_circ_299392,RMVar_hsa_circ_329552,RMVar_hsa_circ_9439,RMVar_hsa_circ_230952,RMVar_hsa_circ_230954,RMVar_hsa_circ_230955,RMVar_hsa_circ_230953,RMVar_hsa_circ_71306 54018 RMVar_ID_54018 Human_SNP_ID_861539065 A-to-I Human chr5 + 176309031 176309031 176309031 TCTTCTCTGGAATAAAGCAGGAGACAAAATGGAGAAAGATGAAAATATCCAGTGTAAAGTTACTT TCTTCTCTGGAATAAAGCAGGAGACAAAATGGGGAAAGATGAAAATATCCAGTGTAAAGTTACTT A G SIMC1 Ensembl:ENSG00000170085 Protein coding intron GSE100210 HepG2 cell line chr5:176309030..176309031 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 5 haematopoietic and lymphoid tissue RMVar_hsa_circ_58004,RMVar_hsa_circ_63765,RMVar_hsa_circ_306548,RMVar_hsa_circ_309390,RMVar_hsa_circ_236342,RMVar_hsa_circ_322535 54019 RMVar_ID_54019 Human_SNP_ID_861545317 A-to-I Human chr5 - 80157631 80157631 80157631 AAGCAGGCTGCGTGGTGCAGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCTGAGGCAGGA AAGCAGGCTGCGTGGTGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGA T C SERINC5 Ensembl:ENSG00000164300 Protein coding intron GSE47997 K562 cells&HepG2 cells chr5:80157630..80157631 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - RMVar_hsa_circ_232783,RMVar_hsa_circ_269699,RMVar_hsa_circ_232780,RMVar_hsa_circ_271981,RMVar_hsa_circ_306297,RMVar_hsa_circ_342614,RMVar_hsa_circ_302416,RMVar_hsa_circ_286119,RMVar_hsa_circ_68477,RMVar_hsa_circ_232781,RMVar_hsa_circ_232782,RMVar_hsa_circ_66187,RMVar_hsa_circ_265892,RMVar_hsa_circ_340479,RMVar_hsa_circ_367038,RMVar_hsa_circ_311422,RMVar_hsa_circ_5435,RMVar_hsa_circ_50497,RMVar_hsa_circ_232787 54020 RMVar_ID_54020 Human_SNP_ID_861664647 A-to-I Human chr5 + 82063041 82063041 82063041 TAGTTTTTCATTTTAAAATACCTCAGATGGCCAGGTATGGTGGCTCACACCTGTAATCCCAGTGC TAGTTTTTCATTTTAAAATACCTCAGATGGCCTGGTATGGTGGCTCACACCTGTAATCCCAGTGC A T ATG10 Ensembl:ENSG00000152348 Protein coding intron GSE100210 HepG2 cell line chr5:82063040..82063041 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 NKTL 1 - RMVar_hsa_circ_121266,RMVar_hsa_circ_232940,RMVar_hsa_circ_232939,RMVar_hsa_circ_303117,RMVar_hsa_circ_355139,RMVar_hsa_circ_125281,RMVar_hsa_circ_232942,RMVar_hsa_circ_232943 54021 RMVar_ID_54021 Human_SNP_ID_861672039 A-to-I Human chr5 + 157310064 157310064 157310064 AAGGGCTCAGAGCACAGCCACGCCCCTTGTCCAGCCCAGCAGTGACTCGCATGTCCTCTCAGCAG AAGGGCTCAGAGCACAGCCACGCCCCTTGTCCCGCCCAGCAGTGACTCGCATGTCCTCTCAGCAG A C CYFIP2 Ensembl:ENSG00000055163 Protein coding intron GSE107867 ASD brains,frontal_cortex chr5:157310063..157310064 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_18837132 RMVar_hsa_circ_1015,RMVar_hsa_circ_310703,RMVar_hsa_circ_344306,RMVar_hsa_circ_49501,RMVar_hsa_circ_85272,RMVar_hsa_circ_31847,RMVar_hsa_circ_115477,RMVar_hsa_circ_105680,RMVar_hsa_circ_99611,RMVar_hsa_circ_101456,RMVar_hsa_circ_87019,RMVar_hsa_circ_235798,RMVar_hsa_circ_76709,RMVar_hsa_circ_22225,RMVar_hsa_circ_235800,RMVar_hsa_circ_235801,RMVar_hsa_circ_235799,RMVar_hsa_circ_235796,RMVar_hsa_circ_235797,RMVar_hsa_circ_235795,RMVar_hsa_circ_348540 54022 RMVar_ID_54022 Human_SNP_ID_861722931 A-to-I Human chr5 + 140854015 140854015 140854015 GTGAGACTCATCTCTGCCAAAAAAAAAAAATTAGCCGGGCATGGTGGCACACATCTCTAGTCCCA GTGAGACTCATCTCTGCCAAAAAAAAAAAATTTGCCGGGCATGGTGGCACACATCTCTAGTCCCA A T PCDHA5,PCDHA3,PCDHA4,PCDHA9,PCDHA7,PCDHA8,PCDHA1,PCDHA6,PCDHA2 Ensembl:ENSG00000204965,Ensembl:ENSG00000255408,Ensembl:ENSG00000204967,Ensembl:ENSG00000204961,Ensembl:ENSG00000204963,Ensembl:ENSG00000204962,Ensembl:ENSG00000204970,Ensembl:ENSG00000081842,Ensembl:ENSG00000204969 Protein coding,Protein coding,Protein coding,Protein coding,Protein coding,Protein coding,Protein coding,Protein coding,Protein coding intron,intron,intron,3'UTR,intron,intron,intron,intron,intron GSE47997 K562 cells&HepG2 cells chr5:140854014..140854015 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 15 oesophagus RMVar_hsa_circ_235058 54023 RMVar_ID_54023 Human_SNP_ID_861755776 A-to-I Human chr5 - 146147001 146147001 146147001 CTCTAGCTCAAAAGGTCTAGGTGGCCAGGCACAGTGGCTCATACCTGTAATCCCAGTACTTTGGG CTCTAGCTCAAAAGGTCTAGGTGGCCAGGCACCGTGGCTCATACCTGTAATCCCAGTACTTTGGG T G LARS1 Ensembl:ENSG00000133706 Protein coding intron GSE107867 ASD brains,frontal_cortex chr5:146147000..146147001 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 4 pancreas Human_RBP_ID_15339395 RMVar_hsa_circ_265072,RMVar_hsa_circ_100747,RMVar_hsa_circ_235238,RMVar_hsa_circ_235236,RMVar_hsa_circ_104530,RMVar_hsa_circ_82362,RMVar_hsa_circ_235241,RMVar_hsa_circ_45752,RMVar_hsa_circ_59644,RMVar_hsa_circ_93600,RMVar_hsa_circ_113570,RMVar_hsa_circ_235243,RMVar_hsa_circ_235244,RMVar_hsa_circ_123626,RMVar_hsa_circ_235245 54024 RMVar_ID_54024 Human_SNP_ID_861796611 A-to-I Human chr5 - 159203632 159203629 159203633 AATTTTAGGTCTTCTCCAAGAAAAAAAAAAAGAAAAAAAAAAACAACATGGCTGCAAAGGAGAAA AATTTTAGGTCTTCTCCAAGAAAAAAAAAAA____AAAAAAAACAACATGGCTGCAAAGGAGAAA TTTTC T RNF145 Ensembl:ENSG00000145860 Protein coding CDS GSE38233 cultured B-cells chr5:159203632..159203633 24183664 RNA-Seq:(High) - Functional Loss DEL TCGA 32..35 33 COAD 1 - Human_RBP_ID_4852228,Human_RBP_ID_23051390,Human_RBP_ID_25933094 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 54025 RMVar_ID_54025 Human_SNP_ID_861827225 A-to-I Human chr5 - 78015467 78015465 78015468 ACAGAATTTCACTCCCTCTGTGATCTTTCAGAAGGTTGTAAATGTAGCCAATGTAGGTGCAGTCC ACAGAATTTCACTCCCTCTGTGATCTTTCAG___GTTGTAAATGTAGCCAATGTAGGTGCAGTCC CCTT C AP3B1 Ensembl:ENSG00000132842 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector chr5:78015466..78015467 29967493 RNA-Seq:(High) - Functional Loss DEL TCGA 32..34 33 COAD 1 - Human_Splice_Rec_666222,Human_Splice_Rec_666223,Human_Splice_Rec_666274,Human_Splice_Rec_666275,Human_Splice_Rec_666282,Human_Splice_Rec_666283,Human_Splice_Rec_666285 Human_miRNA_ID_2243084,Human_miRNA_ID_2244102 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_297246,RMVar_hsa_circ_232637,RMVar_hsa_circ_232643,RMVar_hsa_circ_341697,RMVar_hsa_circ_311135,RMVar_hsa_circ_232645,RMVar_hsa_circ_232646 54026 RMVar_ID_54026 Human_SNP_ID_861838993 A-to-I Human chr5 - 10759844 10759844 10759844 AGGCCGAGGCAGGAGAATGGCTTGAACCCGGGAGGCAGAAGTTGTAGTGAGCCAAGATTGAGCCA AGGCCGAGGCAGGAGAATGGCTTGAACCCGGGGGGCAGAAGTTGTAGTGAGCCAAGATTGAGCCA T C DAP Ensembl:ENSG00000112977 Protein coding intron GSE47997 K562 cells&HepG2 cells chr5:10759843..10759844 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - RMVar_hsa_circ_92360,RMVar_hsa_circ_107577,RMVar_hsa_circ_230272,RMVar_hsa_circ_230273 54027 RMVar_ID_54027 Human_SNP_ID_861878062 A-to-I Human chr5 + 33162324 33162324 33162324 TGGCCCCCGCCGCATCCACACAGTCCGTGTGCAGGGAAGTAACAAGAAATACCGTGCCCTGAGGT TGGCCCCCGCCGCATCCACACAGTCCGTGTGCTGGGAAGTAACAAGAAATACCGTGCCCTGAGGT A T AC010343.1 Ensembl:ENSG00000240376 Pseudogene exon GSE100210 HepG2 cell line chr5:33162323..33162324 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA 33..33 33 LUAD 1 - 54028 RMVar_ID_54028 Human_SNP_ID_861878068 A-to-I Human chr5 + 33162324 33162324 33162324 TGGCCCCCGCCGCATCCACACAGTCCGTGTGCAGGGAAGTAACAAGAAATACCGTGCCCTGAGGT TGGCCCCCGCCGCATCCACACAGTCCGTGTGCGGGGAAGTAACAAGAAATACCGTGCCCTGAGGT A G AC010343.1 Ensembl:ENSG00000240376 Pseudogene exon GSE100210 HepG2 cell line chr5:33162323..33162324 29129909 RNA-Seq:(High) rs548437212 Functional Loss SNV ICGC 33..33 33 STAD 1 - 54029 RMVar_ID_54029 Human_SNP_ID_861909992 A-to-I Human chr5 + 177593669 177593669 177593669 TACCTTCCTCCAGGTCATCCTGGCCCGGCAGTATGGCTCCGAGGGCAGGTTCACTTTCACTTCCC TACCTTCCTCCAGGTCATCCTGGCCCGGCAGTGTGGCTCCGAGGGCAGGTTCACTTTCACTTCCC A G TMED9 Ensembl:ENSG00000184840 Protein coding CDS GSE100210 HepG2 cell line chr5:177593668..177593669 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 stomach adenocarcinoma 1 stomach Human_RBP_ID_639072,Human_RBP_ID_1212084,Human_RBP_ID_4825357,Human_RBP_ID_18045583,Human_RBP_ID_22460339,Human_RBP_ID_22613883,Human_RBP_ID_22681087,Human_RBP_ID_22771539 Human_Splice_Rec_726230,Human_Splice_Rec_726236,Human_Splice_Rec_726240,Human_Splice_Rec_726244,Human_Splice_Rec_726250,Human_Splice_Rec_726251 RMVar_hsa_circ_87084,RMVar_hsa_circ_112447,RMVar_hsa_circ_236546,RMVar_hsa_circ_116651,RMVar_hsa_circ_236547,RMVar_hsa_circ_236548 54030 RMVar_ID_54030 Human_SNP_ID_861925453 A-to-I Human chr5 + 176308893 176308893 176308893 GTGTTTACCAAGAATCTGTGCAGTCAGATGTCAGCAGTCAGCGGGCCTCTTCTACAGTGGTTGGA GTGTTTACCAAGAATCTGTGCAGTCAGATGTCGGCAGTCAGCGGGCCTCTTCTACAGTGGTTGGA A G BRCC3P1,SIMC1 Ensembl:ENSG00000251667,Ensembl:ENSG00000170085 Pseudogene,Protein coding exon,intron GSE100210 HepG2 cell line chr5:176308892..176308893 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 10 haematopoietic and lymphoid tissue Human_miRNA_ID_1881508,Human_miRNA_ID_1899038 RMVar_hsa_circ_58004,RMVar_hsa_circ_63765,RMVar_hsa_circ_306548,RMVar_hsa_circ_309390,RMVar_hsa_circ_236342,RMVar_hsa_circ_322535 54031 RMVar_ID_54031 Human_SNP_ID_861967845 A-to-I Human chr5 + 177147245 177147245 177147245 CTCCCACCTCAGCCTCCTGATTAGCTGCGACTACAGGCACTTGCCACCATGCCCCACTAATTTTT CTCCCACCTCAGCCTCCTGATTAGCTGCGACTGCAGGCACTTGCCACCATGCCCCACTAATTTTT A G NSD1 Ensembl:ENSG00000165671 Protein coding intron GSE38233 cultured B-cells chr5:177147244..177147245 24183664 RNA-Seq:(High) rs76515674 Functional Loss SNV ICGC 33..33 33 LAML 1 - Clinvar_Rec_42 RMVar_hsa_circ_6376,RMVar_hsa_circ_109213,RMVar_hsa_circ_296651,RMVar_hsa_circ_322685,RMVar_hsa_circ_374749,RMVar_hsa_circ_236431,RMVar_hsa_circ_99866,RMVar_hsa_circ_236434,RMVar_hsa_circ_236435,RMVar_hsa_circ_236436,RMVar_hsa_circ_54322,RMVar_hsa_circ_325752,RMVar_hsa_circ_331791,RMVar_hsa_circ_97595,RMVar_hsa_circ_236437,RMVar_hsa_circ_236438 54032 RMVar_ID_54032 Human_SNP_ID_861973464 A-to-I Human chr5 - 157477845 157477845 157477845 TTTCTGGTTGGAGTGTTTTTTTGTATTGCCATAGTCCCTTCCCCCTGAAGCAATAGCCCCTCCCC TTTCTGGTTGGAGTGTTTTTTTGTATTGCCATGGTCCCTTCCCCCTGAAGCAATAGCCCCTCCCC T C ADAM19 Ensembl:ENSG00000135074 Protein coding intron GSE38233 cultured B-cells chr5:157477844..157477845 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue RMVar_hsa_circ_118709,RMVar_hsa_circ_235821,RMVar_hsa_circ_235822,RMVar_hsa_circ_76268 54033 RMVar_ID_54033 Human_SNP_ID_861988128 A-to-I Human chr5 - 161421199 161421199 161421199 TCACAGGTGGTGGTCCTTAATAAATGTCCTTCAGGGTCTGCTTCTGGAAAACCCAACACTAGACA TCACAGGTGGTGGTCCTTAATAAATGTCCTTCGGGGTCTGCTTCTGGAAAACCCAACACTAGACA T C GABRB2 Ensembl:ENSG00000145864 Protein coding intron GSE107867 ASD brains,cerebellum chr5:161421198..161421199 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 8 pancreas RMVar_hsa_circ_31500,RMVar_hsa_circ_235934,RMVar_hsa_circ_297425 54034 RMVar_ID_54034 Human_SNP_ID_862016146 A-to-I Human chr5 + 133100638 133100638 133100638 GAAACCCTGTCTCTACTAAAAATACAAAAATTAGCCGAGCGTGGTGGCGGGTGCCTGTAGTCCCA GAAACCCTGTCTCTACTAAAAATACAAAAATTGGCCGAGCGTGGTGGCGGGTGCCTGTAGTCCCA A G HSPA4 Ensembl:ENSG00000170606 Protein coding intron GSE100210 HepG2 cell line chr5:133100637..133100638 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_10181030 RMVar_hsa_circ_14806,RMVar_hsa_circ_121056,RMVar_hsa_circ_96684,RMVar_hsa_circ_234419,RMVar_hsa_circ_90522,RMVar_hsa_circ_234418,RMVar_hsa_circ_234429,RMVar_hsa_circ_341278,RMVar_hsa_circ_357962,RMVar_hsa_circ_353504,RMVar_hsa_circ_357048 54035 RMVar_ID_54035 Human_SNP_ID_862033242 A-to-I Human chr5 + 128110763 128110763 128110763 CTGAGCGATCTGCTAGAAAAACTTAAATGGACAAAAGATCACAATGAAGAGGCCAAAAAGATAGC CTGAGCGATCTGCTAGAAAAACTTAAATGGACGAAAGATCACAATGAAGAGGCCAAAAAGATAGC A G SLC12A2,KDELC1P1 Ensembl:ENSG00000064651,Ensembl:ENSG00000250329 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line chr5:128110762..128110763 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue RMVar_hsa_circ_100540,RMVar_hsa_circ_234127 54036 RMVar_ID_54036 Human_SNP_ID_862043244 A-to-I Human chr5 - 59423332 59423332 59423332 ATTACAATTACAAAATACATAAATATGTGATTACAATTGTGAGAACTGCTCAAAAGGAAACAAGG ATTACAATTACAAAATACATAAATATGTGATTGCAATTGTGAGAACTGCTCAAAAGGAAACAAGG T C PDE4D Ensembl:ENSG00000113448 Protein coding intron GSE100210 HepG2 cell line chr5:59423331..59423332 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PRAD 2 - RMVar_hsa_circ_25249,RMVar_hsa_circ_7785,RMVar_hsa_circ_26973,RMVar_hsa_circ_231584,RMVar_hsa_circ_231590,RMVar_hsa_circ_231585,RMVar_hsa_circ_231587,RMVar_hsa_circ_231586 54037 RMVar_ID_54037 Human_SNP_ID_862067076 A-to-I Human chr5 - 91309686 91309686 91309686 CTATGCATATAATCCCAACTCTTTGAGAGGCCAGGGTGGGTGGATTGCTTGAGTCCAGGAATTCG CTATGCATATAATCCCAACTCTTTGAGAGGCCGGGGTGGGTGGATTGCTTGAGTCCAGGAATTCG T C LUCAT1 Ensembl:ENSG00000248323 lincRNA intron GSE100210 HepG2 cell line chr5:91309685..91309686 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 54038 RMVar_ID_54038 Human_SNP_ID_862081778 A-to-I Human chr5 - 134927780 134927780 134927780 CACAATCATGGCAAGCCAACGCCACTTATCCAATGAACCACTATCACGAAAAAAACTCTACCTCT CACAATCATGGCAAGCCAACGCCACTTATCCAGTGAACCACTATCACGAAAAAAACTCTACCTCT T C MTND4P12 Ensembl:ENSG00000247627 Pseudogene exon GSE100210 HepG2 cell line chr5:134927779..134927780 29129909 RNA-Seq:(High) rs12332606 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_3784706,Human_RBP_ID_4847332,Human_RBP_ID_5214838,Human_RBP_ID_5641143,Human_RBP_ID_8894364,Human_RBP_ID_9341537,Human_RBP_ID_9437212,Human_RBP_ID_10232000,Human_RBP_ID_17090681,Human_RBP_ID_17196269,Human_RBP_ID_17209363,Human_RBP_ID_17416415,Human_RBP_ID_17584740,Human_RBP_ID_18170750,Human_RBP_ID_18538373,Human_RBP_ID_18544890,Human_RBP_ID_18927262,Human_RBP_ID_18956906,Human_RBP_ID_21120179,Human_RBP_ID_21945207,Human_RBP_ID_21990527,Human_RBP_ID_26521472 Human_miRNA_ID_1827577 54039 RMVar_ID_54039 Human_SNP_ID_862091210 A-to-I Human chr5 - 25910230 25910230 25910230 TCATTGAAAGAAATGCTCCTGATTTCACTCCAAGGAAAGCCTATCTTGGGAGTTAGTCTGTCATG TCATTGAAAGAAATGCTCCTGATTTCACTCCAGGGAAAGCCTATCTTGGGAGTTAGTCTGTCATG T C - - Other Unknown GSE100210 HepG2 cell line chr5:25910229..25910230 29129909 RNA-Seq:(High) rs942831160 Functional Loss SNV ICGC 33..33 33 LAML 1 - 54040 RMVar_ID_54040 Human_SNP_ID_862137920 A-to-I Human chr5 - 77785111 77785111 77785111 CAGATCTTCTCCATGTCGTCCCAGTTGGTGACAATGCCGTGCTCAATGGGGTACTTCAGGGTGAG CAGATCTTCTCCATGTCGTCCCAGTTGGTGACGATGCCGTGCTCAATGGGGTACTTCAGGGTGAG T C TBCA Ensembl:ENSG00000171530 Protein coding intron GSE100210 HepG2 cell line chr5:77785110..77785111 29129909 RNA-Seq:(High) rs972908054 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue 54041 RMVar_ID_54041 Human_SNP_ID_862151521 A-to-I Human chr5 - 10759928 10759928 10759928 TAACATGGTGAAACCCCATCTCTACTAAAAGTAGAAAAATTAGCTGGGCATGGTGGCGGGCGCCT TAACATGGTGAAACCCCATCTCTACTAAAAGTGGAAAAATTAGCTGGGCATGGTGGCGGGCGCCT T C DAP Ensembl:ENSG00000112977 Protein coding intron GSE38233 cultured B-cells chr5:10759927..10759928 24183664 RNA-Seq:(High) rs769553782 Functional Loss SNV ICGC 33..33 33 MALY 1 - RMVar_hsa_circ_92360,RMVar_hsa_circ_107577,RMVar_hsa_circ_230272,RMVar_hsa_circ_230273 54042 RMVar_ID_54042 Human_SNP_ID_862239834 A-to-I Human chr5 + 134680976 134680976 134680976 CAATAATTAGCCGGGTGTGGTGGCGGGCACCTATAATCCCAGCTACTCGGGAGGCTGAGGCAGGA CAATAATTAGCCGGGTGTGGTGGCGGGCACCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGA A G SEC24A Ensembl:ENSG00000113615 Protein coding intron GSE38233 cultured B-cells chr5:134680975..134680976 24183664 RNA-Seq:(High) rs1342111286 Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_63156,RMVar_hsa_circ_367561,RMVar_hsa_circ_366335,RMVar_hsa_circ_119701,RMVar_hsa_circ_123001,RMVar_hsa_circ_100845,RMVar_hsa_circ_234533,RMVar_hsa_circ_90206,RMVar_hsa_circ_234524,RMVar_hsa_circ_234526,RMVar_hsa_circ_234527,RMVar_hsa_circ_234528,RMVar_hsa_circ_234525,RMVar_hsa_circ_316928,RMVar_hsa_circ_374082,RMVar_hsa_circ_372661,RMVar_hsa_circ_115390,RMVar_hsa_circ_110619,RMVar_hsa_circ_86291,RMVar_hsa_circ_234535,RMVar_hsa_circ_234534,RMVar_hsa_circ_234529,RMVar_hsa_circ_234531,RMVar_hsa_circ_234532,RMVar_hsa_circ_234530,RMVar_hsa_circ_337937,RMVar_hsa_circ_366850,RMVar_hsa_circ_378363,RMVar_hsa_circ_340580,RMVar_hsa_circ_105485,RMVar_hsa_circ_25480,RMVar_hsa_circ_83820,RMVar_hsa_circ_24133,RMVar_hsa_circ_234542,RMVar_hsa_circ_234543,RMVar_hsa_circ_294529,RMVar_hsa_circ_347453,RMVar_hsa_circ_362704,RMVar_hsa_circ_322834,RMVar_hsa_circ_304369,RMVar_hsa_circ_280706,RMVar_hsa_circ_28989,RMVar_hsa_circ_234546,RMVar_hsa_circ_13208,RMVar_hsa_circ_234547,RMVar_hsa_circ_234544,RMVar_hsa_circ_234545,RMVar_hsa_circ_86864,RMVar_hsa_circ_49527,RMVar_hsa_circ_103204,RMVar_hsa_circ_234550,RMVar_hsa_circ_234551,RMVar_hsa_circ_234552,RMVar_hsa_circ_369767,RMVar_hsa_circ_55900,RMVar_hsa_circ_44677,RMVar_hsa_circ_115121,RMVar_hsa_circ_338506,RMVar_hsa_circ_234553,RMVar_hsa_circ_355590,RMVar_hsa_circ_287636,RMVar_hsa_circ_68346,RMVar_hsa_circ_234554,RMVar_hsa_circ_234556,RMVar_hsa_circ_234557,RMVar_hsa_circ_234555 54043 RMVar_ID_54043 Human_SNP_ID_862280171 A-to-I Human chr5 + 144346919 144346919 144346919 TTGGTTTCCTATGCTTGTTTCCATACTCAAGAAATCTTTGCCCAGACCCAAGTCCTGGAGATTTT TTGGTTTCCTATGCTTGTTTCCATACTCAAGACATCTTTGCCCAGACCCAAGTCCTGGAGATTTT A C KCTD16 Ensembl:ENSG00000183775 Protein coding intron GSE107867 ASD brains,frontal_cortex chr5:144346919..144346920 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 54044 RMVar_ID_54044 Human_SNP_ID_867183207 A-to-I Human chr7 - 102493273 102493273 102493273 CTCCCTCCCTGGCCTGGCAGAGCTGGACCTGCAGCGGACGCTGAGTTTGCAGGCGCCACCTGTGA CTCCCTCCCTGGCCTGGCAGAGCTGGACCTGCGGCGGACGCTGAGTTTGCAGGCGCCACCTGTGA T C RASA4B Ensembl:ENSG00000170667 Protein coding exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr7:102493272..102493273 30559470 RNA-Seq:(High) rs1203767469 Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_Splice_Rec_903692,Human_Splice_Rec_903704,Human_Splice_Rec_903742,Human_Splice_Rec_903756,Human_Splice_Rec_903802 RMVar_hsa_circ_100408,RMVar_hsa_circ_247338,RMVar_hsa_circ_119474,RMVar_hsa_circ_247340 54045 RMVar_ID_54045 Human_SNP_ID_867188216 A-to-I Human chr7 + 154243684 154243684 154243684 GGGCATGGTGGCGGGTGCCTGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATGATGTGAA GGGCATGGTGGCGGGTGCCTGTAGTCCCAGCTGCTCAGGAGGCTGAGGCAGGAGAATGATGTGAA A G DPP6 Ensembl:ENSG00000130226 Protein coding intron GSE47997 K562 cells&HepG2 cells chr7:154243683..154243684 23474544 RNA-Seq:(High) rs1397921943 Functional Loss SNV ICGC 33..33 33 LICA 1 - 54046 RMVar_ID_54046 Human_SNP_ID_867268848 A-to-I Human chr7 - 73471010 73471010 73471010 GATATTTTGGCTGGGTGTGGTGGCTCACGCCTATAATCCCAGCACTTTGAGGGGCCGAGACGGGT GATATTTTGGCTGGGTGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGAGGGGCCGAGACGGGT T C BAZ1B Ensembl:ENSG00000009954 Protein coding intron GSE38233 cultured B-cells chr7:73471009..73471010 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 3 prostate Human_RBP_ID_26115716 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 54047 RMVar_ID_54047 Human_SNP_ID_867285907 A-to-I Human chr7 + 128653944 128653944 128653944 GGGTCTACAAAGGCCGGCGGGAGCTGAGCCAAAAGAGCTTGTTTGCTGGGAGGCGGGAGATGCAG GGGTCTACAAAGGCCGGCGGGAGCTGAGCCAAGAGAGCTTGTTTGCTGGGAGGCGGGAGATGCAG A G LINC01000,LINC01000:2 RNACentral:URS0000D58990,RNACentral:URS000075B9E1 lincRNA,lincRNA intron,exon GSE107867 ASD brains,cerebellum chr7:128653944..128653945 30559470 RNA-Seq:(High) - Functional Loss SNV TCGA 33..33 33 UCEC 1 - 54048 RMVar_ID_54048 Human_SNP_ID_867331232 A-to-I Human chr7 - 104999039 104999039 104999039 AGGTGCCTGCAACCACACCTGGCTAATTTTTTATTTTTAGTAGAGACAGGGTTTCACCATGTTGG AGGTGCCTGCAACCACACCTGGCTAATTTTTTTTTTTTAGTAGAGACAGGGTTTCACCATGTTGG T A LINC01004 Ensembl:ENSG00000228393 lincRNA intron GSE100210 HepG2 cell line chr7:104999038..104999039 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 54049 RMVar_ID_54049 Human_SNP_ID_867388450 A-to-I Human chr7 - 6464273 6464273 6464273 CTCGTGATCCGCACACCTCAGCCTCCCAAAGTATTGGGATTACAGGCGTGAGCCACCACGCCTAG CTCGTGATCCGCACACCTCAGCCTCCCAAAGTGTTGGGATTACAGGCGTGAGCCACCACGCCTAG T C KDELR2,DAGLB Ensembl:ENSG00000136240,Ensembl:ENSG00000164535 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells chr7:6464272..6464273 24183664 RNA-Seq:(High) rs1269966756 Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_miRNA_ID_2418217 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 54050 RMVar_ID_54050 Human_SNP_ID_867417475 A-to-I Human chr7 - 111480216 111480216 111480216 AGCTGGGCGTGGTGGTGGGCGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCG AGCTGGGCGTGGTGGTGGGCGCCTGTAGTCCCCGCTACTCGGGAGGCTGAGGCAGGAGAATGGCG T G IMMP2L Ensembl:ENSG00000184903 Protein coding intron GSE47997 K562 cells&HepG2 cells chr7:111480215..111480216 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - Human_RBP_ID_175394 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_247834,RMVar_hsa_circ_62976,RMVar_hsa_circ_326034 54051 RMVar_ID_54051 Human_SNP_ID_867436293 A-to-I Human chr7 - 129890081 129890081 129890081 TCACCCAGGCTGGAGTTCAGTAGTGTCATCATAGCTTACTACAGACTCAAACTCCTGGGCTCCAG TCACCCAGGCTGGAGTTCAGTAGTGTCATCATGGCTTACTACAGACTCAAACTCCTGGGCTCCAG T C UBE2H Ensembl:ENSG00000186591 Protein coding intron GSE100210 HepG2 cell line chr7:129890080..129890081 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 UTCA,endometrium carcinosarcoma-malignant_mesodermal_mixed_tumour 3 uterus 54052 RMVar_ID_54052 Human_SNP_ID_867458961 A-to-I Human chr7 - 72791603 72791603 72791603 CCAGCTAATTTTTTGTGTTTTTAGTAGAGACGAGGTTTCACCATGTTAGCCAGGATGGTCCCGAT CCAGCTAATTTTTTGTGTTTTTAGTAGAGACGGGGTTTCACCATGTTAGCCAGGATGGTCCCGAT T C TYW1B Ensembl:ENSG00000277149 Protein coding intron GSE47997 K562 cells&HepG2 cells chr7:72791602..72791603 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - RMVar_hsa_circ_16897,RMVar_hsa_circ_64202,RMVar_hsa_circ_65751,RMVar_hsa_circ_75477 54053 RMVar_ID_54053 Human_SNP_ID_867500672 A-to-I Human chr7 + 129127594 129127594 129127594 CTCATCAAAAACCCAACGGAGCGGGCGGACCTAAAGATGCTCACAAACCACGCCTTCATCAAGCG CTCATCAAAAACCCAACGGAGCGGGCGGACCTGAAGATGCTCACAAACCACGCCTTCATCAAGCG A G AC011005.1 Ensembl:ENSG00000230626 Protein coding CDS GSE100210 HepG2 cell line chr7:129127593..129127594 29129909 RNA-Seq:(High) rs917838477 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue Human_Splice_Rec_921873 54054 RMVar_ID_54054 Human_SNP_ID_867517749 A-to-I Human chr7 - 100078234 100078234 100078234 CCTCAGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGTGCCCAGCCTGGGAGTAGTCTT CCTCAGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGTGCCCAGCCTGGGAGTAGTCTT T C ZNF3 Ensembl:ENSG00000166526 Protein coding intron GSE38233 cultured B-cells chr7:100078233..100078234 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_273088,RMVar_hsa_circ_247003,RMVar_hsa_circ_329854,RMVar_hsa_circ_269835,RMVar_hsa_circ_344399,RMVar_hsa_circ_247005 54055 RMVar_ID_54055 Human_SNP_ID_867519804 A-to-I Human chr7 - 32472079 32472079 32472079 CCCTTTGCAGTGTCATAGATACCAAAGTAGGCAGCTCGGTAGATGATAATACCCTGCACAGACAC CCCTTTGCAGTGTCATAGATACCAAAGTAGGCGGCTCGGTAGATGATAATACCCTGCACAGACAC T C - - Other Unknown GSE100210 HepG2 cell line chr7:32472078..32472079 29129909 RNA-Seq:(High) rs879193920 Functional Loss SNV ICGC 33..33 33 LAML 1 - 54056 RMVar_ID_54056 Human_SNP_ID_867521082 A-to-I Human chr7 + 139368591 139368591 139368591 TGAAACCTGTCTCTACTAAAAATATAAAAATTAGCCAGATGTGGTGGTGGGTGCCTGTAATCCCA TGAAACCTGTCTCTACTAAAAATATAAAAATTGGCCAGATGTGGTGGTGGGTGCCTGTAATCCCA A G FMC1-LUC7L2,LUC7L2 Ensembl:ENSG00000269955,Ensembl:ENSG00000146963 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells chr7:139368590..139368591 24183664 RNA-Seq:(High) rs10954645 Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 4 liver RMVar_hsa_circ_34626 54057 RMVar_ID_54057 Human_SNP_ID_867548368 A-to-I Human chr7 - 16089311 16089311 16089311 GCATACACACATATATTTATATACGTACGCATACACACATATATGTATATACGTACGCATACACA GCATACACACATATATTTATATACGTACGCATGCACACATATATGTATATACGTACGCATACACA T C CRPPA Ensembl:ENSG00000214960 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells chr7:16089310..16089311 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_112717,RMVar_hsa_circ_116458,RMVar_hsa_circ_243875,RMVar_hsa_circ_243876 54058 RMVar_ID_54058 Human_SNP_ID_867568362 A-to-I Human chr7 + 129420554 129420554 129420554 CAGACTGGAGTGCAGTGGCACAATCTCAGCTCACTGCAGACTCGACTTCCTGGGCTCAAGCATTC CAGACTGGAGTGCAGTGGCACAATCTCAGCTCTCTGCAGACTCGACTTCCTGGGCTCAAGCATTC A T AHCYL2 Ensembl:ENSG00000158467 Protein coding intron GSE47997 K562 cells&HepG2 cells chr7:129420553..129420554 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - RMVar_hsa_circ_268170,RMVar_hsa_circ_36170,RMVar_hsa_circ_15442 54059 RMVar_ID_54059 Human_SNP_ID_867575623 A-to-I Human chr7 + 44467961 44467961 44467961 GATCGTCAAAAAGAGAACCAAGAAGTTCATCCAGCACCAGTCAGACCAATATGTCAAAATTAAGC GATCGTCAAAAAGAGAACCAAGAAGTTCATCCGGCACCAGTCAGACCAATATGTCAAAATTAAGC A G AC004453.1 Ensembl:ENSG00000146677 Pseudogene exon GSE100210 HepG2 cell line chr7:44467960..44467961 29129909 RNA-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 54060 RMVar_ID_54060 Human_SNP_ID_867582197 A-to-I Human chr7 + 158623416 158623416 158623416 ATAAAAACTCAGCTTCCGGTCTTTATTGTTTCATCCCCGGCAGTTCTTACAACAAATCGCCGCGC ATAAAAACTCAGCTTCCGGTCTTTATTGTTTCGTCCCCGGCAGTTCTTACAACAAATCGCCGCGC A G - - Other Unknown GSE100210 HepG2 cell line chr7:158623415..158623416 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 2 - 54061 RMVar_ID_54061 Human_SNP_ID_867608416 A-to-I Human chr7 + 154336150 154336150 154336150 GCCTGCATTCCAGGACATCTTGCAGCCTCTGAAATGCAGCGTGGCACACAGCACTCAGGTTCCTG GCCTGCATTCCAGGACATCTTGCAGCCTCTGACATGCAGCGTGGCACACAGCACTCAGGTTCCTG A C DPP6 Ensembl:ENSG00000130226 Protein coding intron GSE107867 ASD brains,cerebellum chr7:154336150..154336151 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 54062 RMVar_ID_54062 Human_SNP_ID_867653495 A-to-I Human chr7 + 66804183 66804183 66804183 GTAGCTCACTGCAGCCTCAACCTCTTGGGCTCAAGCCATCCTTCTGCCTCAGCCTTTCCAGTAGT GTAGCTCACTGCAGCCTCAACCTCTTGGGCTCTAGCCATCCTTCTGCCTCAGCCTTTCCAGTAGT A T AC027644.4,RABGEF1 Ensembl:ENSG00000284461,Ensembl:ENSG00000154710 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line chr7:66804183..66804184 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_miRNA_ID_2042822,Human_miRNA_ID_2044973 RMVar_hsa_circ_11472,RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_245373,RMVar_hsa_circ_12986,RMVar_hsa_circ_377698,RMVar_hsa_circ_300161,RMVar_hsa_circ_245378,RMVar_hsa_circ_245372,RMVar_hsa_circ_377787,RMVar_hsa_circ_319250,RMVar_hsa_circ_278625,RMVar_hsa_circ_126240,RMVar_hsa_circ_245383,RMVar_hsa_circ_279002,RMVar_hsa_circ_245385,RMVar_hsa_circ_245386,RMVar_hsa_circ_271655 54063 RMVar_ID_54063 Human_SNP_ID_867731555 A-to-I Human chr7 - 16089432 16089432 16089432 ATACACATATATGTATGCACGTACATATATACACATATATGTATGTACGTACATATATACACATT ATACACATATATGTATGCACGTACATATATACCCATATATGTATGTACGTACATATATACACATT T G CRPPA Ensembl:ENSG00000214960 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells chr7:16089431..16089432 23474544 RNA-Seq:(High) rs930725908 Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_17578351 RMVar_hsa_circ_112717,RMVar_hsa_circ_116458,RMVar_hsa_circ_243875,RMVar_hsa_circ_243876 54064 RMVar_ID_54064 Human_SNP_ID_867782642 A-to-I Human chr7 - 121441228 121441228 121441228 TGCTGAAGAGGTTGTTTATGAGTGCACCAACCAGCCACCTCTGTCCCTTTCCCGGATGATCCCGA TGCTGAAGAGGTTGTTTATGAGTGCACCAACCGGCCACCTCTGTCCCTTTCCCGGATGATCCCGA T C AC074085.2 Ensembl:ENSG00000234985 Pseudogene exon GSE100210 HepG2 cell line chr7:121441227..121441228 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 54065 RMVar_ID_54065 Human_SNP_ID_867782803 A-to-I Human chr7 + 75415590 75415590 75415590 GCTCAGCTCACCCCTGCTCTGCCCTCTGCCCTAGGAAGATCTTTGCCTTTGACCTGGATGCCAAG GCTCAGCTCACCCCTGCTCTGCCCTCTGCCCTCGGAAGATCTTTGCCTTTGACCTGGATGCCAAG A C NSUN5P1 Ensembl:ENSG00000223705 Pseudogene intron GSE105773 Glioblastoma cells,U87MG chr7:75415589..75415590 29724793 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC 33..33 33 SKCM 2 - 54066 RMVar_ID_54066 Human_SNP_ID_867818533 A-to-I Human chr7 - 105125821 105125819 105125821 AACTGCTGGGGAAAGTCCCTCGAAAATACGCTATGTTGGGGAAATACTCCAAGGAGTTTTTCACC AACTGCTGGGGAAAGTCCCTCGAAAATACGCT__GTTGGGGAAATACTCCAAGGAGTTTTTCACC CAT C SRPK2 Ensembl:ENSG00000135250 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr7:105125820..105125821 30559470 RNA-Seq:(High) - Functional Loss DEL ICGC 33..34 33 CHOL 1 - Human_RBP_ID_26055597 Human_Splice_Rec_907046,Human_Splice_Rec_907047,Human_Splice_Rec_907132,Human_Splice_Rec_907133,Human_Splice_Rec_907174,Human_Splice_Rec_907175 RMVar_hsa_circ_28438,RMVar_hsa_circ_91004,RMVar_hsa_circ_99536,RMVar_hsa_circ_124459,RMVar_hsa_circ_247556,RMVar_hsa_circ_247558,RMVar_hsa_circ_80610,RMVar_hsa_circ_247557,RMVar_hsa_circ_247555,RMVar_hsa_circ_28469,RMVar_hsa_circ_3129,RMVar_hsa_circ_55653,RMVar_hsa_circ_65667 54067 RMVar_ID_54067 Human_SNP_ID_867895995 A-to-I Human chr7 - 5330370 5330370 5330370 CAATTAGCTGGGAGTGGTGGTGATCAGTGCCTATAGTCCCACCTACTCTGGAAGCTGGGGCAGGG CAATTAGCTGGGAGTGGTGGTGATCAGTGCCTGTAGTCCCACCTACTCTGGAAGCTGGGGCAGGG T C TNRC18 Ensembl:ENSG00000182095 Protein coding intron GSE38233 cultured B-cells chr7:5330369..5330370 24183664 RNA-Seq:(High) rs4236387 Functional Loss SNV ICGC 33..33 33 ESCA 1 - 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 54068 RMVar_ID_54068 Human_SNP_ID_867948622 A-to-I Human chr7 + 4142403 4142403 4142403 CAGGCTGGAGTGCAGTGACGTGATCTCGGCTCACCGCAGCCTCCGCCTCCCGGGTTCAAGCGATT CAGGCTGGAGTGCAGTGACGTGATCTCGGCTCCCCGCAGCCTCCGCCTCCCGGGTTCAAGCGATT A C SDK1 Ensembl:ENSG00000146555 Protein coding intron GSE100210 HepG2 cell line chr7:4142402..4142403 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - RMVar_hsa_circ_102650,RMVar_hsa_circ_4180,RMVar_hsa_circ_243404,RMVar_hsa_circ_79944,RMVar_hsa_circ_89885,RMVar_hsa_circ_243428,RMVar_hsa_circ_243430,RMVar_hsa_circ_268977,RMVar_hsa_circ_39884 54069 RMVar_ID_54069 Human_SNP_ID_867986912 A-to-I Human chr7 + 66658942 66658942 66658942 TATTTTTAGCGGAGACGGGGTTTCACTGTGTTAGCCAGGATGATCTCTATCTCCTGACCTCATGA TATTTTTAGCGGAGACGGGGTTTCACTGTGTTGGCCAGGATGATCTCTATCTCCTGACCTCATGA A G AC027644.4,AC006001.2 Ensembl:ENSG00000284461,Ensembl:ENSG00000226824 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line chr7:66658941..66658942 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_245369,RMVar_hsa_circ_80384 54070 RMVar_ID_54070 Human_SNP_ID_868011464 A-to-I Human chr7 + 101822778 101822778 101822778 CAAAAATTAGCCTGGCGTGGTGGCGCATATCCATAATCCCAGATACTCGGCAGGCTGAGGCATGA CAAAAATTAGCCTGGCGTGGTGGCGCATATCCTTAATCCCAGATACTCGGCAGGCTGAGGCATGA A T CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE100210 HepG2 cell line chr7:101822777..101822778 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_3030884,Human_RBP_ID_15947283,Human_RBP_ID_26051970 54071 RMVar_ID_54071 Human_SNP_ID_868014412 A-to-I Human chr7 - 5370531 5370531 5370531 CCCTGGCGGCAGCTGCGGAGCTGCCCCAGGCCAGGCCTCTGCCCTCCCCGGGTGCTGCTGGAGCC CCCTGGCGGCAGCTGCGGAGCTGCCCCAGGCCGGGCCTCTGCCCTCCCCGGGTGCTGCTGGAGCC T C TNRC18 Ensembl:ENSG00000182095 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector chr7:5370530..5370531 29967493 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_3971813,Human_RBP_ID_5533398,Human_RBP_ID_8914281,Human_RBP_ID_9311191 Human_miRNA_ID_2272082 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 54072 RMVar_ID_54072 Human_SNP_ID_868018652 A-to-I Human chr7 - 82952183 82952183 82952183 ATGAGTCTACTTCAAGTGTGATGACCAAAATAATAGAAGATGAAAAACCCGTTGATTTAACCGCA ATGAGTCTACTTCAAGTGTGATGACCAAAATATTAGAAGATGAAAAACCCGTTGATTTAACCGCA T A PCLO Ensembl:ENSG00000186472 Protein coding CDS GSE56152 embryonic stem cells,wild type chr7:82952182..82952183 25708366 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 oesophagus squamous_cell_carcinoma 2 oesophagus Human_RBP_ID_18886377 RMVar_hsa_circ_86878,RMVar_hsa_circ_286580,RMVar_hsa_circ_246188 54073 RMVar_ID_54073 Human_SNP_ID_868019654 A-to-I Human chr7 - 140475480 140475480 140475480 TTTTTTTGCATTTTTGATAGAGACAGGGTTTCACCCTGTTGCCTAGGCTGGTCTTGAACTCCTAA TTTTTTTGCATTTTTGATAGAGACAGGGTTTCCCCCTGTTGCCTAGGCTGGTCTTGAACTCCTAA T G MKRN1 Ensembl:ENSG00000133606 Protein coding intron GSE100210 HepG2 cell line chr7:140475479..140475480 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_16045150 54074 RMVar_ID_54074 Human_SNP_ID_868046498 A-to-I Human chr7 + 76521245 76521245 76521245 AAAATTAGCCAGGCATGGTGATGGGCGCCTGTAATTTCAGCTACTTGGGAGGCTGAGGCAGGAGA AAAATTAGCCAGGCATGGTGATGGGCGCCTGTCATTTCAGCTACTTGGGAGGCTGAGGCAGGAGA A C - - Other Unknown GSE100210 HepG2 cell line chr7:76521245..76521246 29129909 RNA-Seq:(High) rs555200172 Functional Loss SNV ICGC 33..33 33 LAML 1 - RMVar_hsa_circ_86873,RMVar_hsa_circ_245848 54075 RMVar_ID_54075 Human_SNP_ID_868080400 A-to-I Human chr7 + 64799296 64799296 64799296 CAAGTGATTTCTCCTGCCGCAGCCTCCTGAGTAGCTGGGATTACAGACATGCGCCACCACGCCCA CAAGTGATTTCTCCTGCCGCAGCCTCCTGAGTGGCTGGGATTACAGACATGCGCCACCACGCCCA A G ZNF138 Ensembl:ENSG00000197008 Protein coding intron GSE100210 HepG2 cell line chr7:64799295..64799296 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 OV 1 - Human_RBP_ID_26109227 54076 RMVar_ID_54076 Human_SNP_ID_868125736 A-to-I Human chr7 - 74231926 74231926 74231926 CCTGTAATCCCAACACTTTGGGAGGCCGAGGCAGGTGGATCACCTGAGGTCAGAAGTTCAAGACC CCTGTAATCCCAACACTTTGGGAGGCCGAGGCGGGTGGATCACCTGAGGTCAGAAGTTCAAGACC T C RFC2 Ensembl:ENSG00000049541 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr7:74231925..74231926 30559470 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine RMVar_hsa_circ_245644,RMVar_hsa_circ_90739 54077 RMVar_ID_54077 Human_SNP_ID_868172694 A-to-I Human chr7 + 7980693 7980693 7980693 GAAGAAGGGCACAATGTCCATGGTGAATAATGACAGTGATCAACATGGATCTCAGTTTCTTATCA GAAGAAGGGCACAATGTCCATGGTGAATAATGGCAGTGATCAACATGGATCTCAGTTTCTTATCA A G AC007161.3,GLCCI1,AC006042.2 Ensembl:ENSG00000283549,Ensembl:ENSG00000106415,Ensembl:ENSG00000233264 lincRNA,Protein coding,Pseudogene intron,intron,exon GSE100210 HepG2 cell line chr7:7980692..7980693 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue Human_RBP_ID_5104640,Human_RBP_ID_8273170,Human_RBP_ID_17543790,Human_RBP_ID_27117005 54078 RMVar_ID_54078 Human_SNP_ID_868222900 A-to-I Human chr7 - 100471657 100471657 100471657 TGGCTCACTGCAACCTCTGCCTCCCAGGTTTAAGCGATTCTCCTGGCTCAGCCTCCCCAGTAGCT TGGCTCACTGCAACCTCTGCCTCCCAGGTTTAGGCGATTCTCCTGGCTCAGCCTCCCCAGTAGCT T C TSC22D4 Ensembl:ENSG00000166925 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr7:100471656..100471657 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_16002 54079 RMVar_ID_54079 Human_SNP_ID_868249332 A-to-I Human chr7 - 44831153 44831153 44831153 TATTTTATTTTTATTTTTTCAGACAAAGTATTACTCTGTCGCCCAGGCTGGCATGCAGTGGCACA TATTTTATTTTTATTTTTTCAGACAAAGTATTGCTCTGTCGCCCAGGCTGGCATGCAGTGGCACA T C H2AZ2 Ensembl:ENSG00000105968 Protein coding intron GSE100210 HepG2 cell line chr7:44831152..44831153 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 COCA 1 - Human_RBP_ID_4942588,Human_RBP_ID_7742501,Human_RBP_ID_8911168,Human_RBP_ID_16166167,Human_RBP_ID_17541491,Human_RBP_ID_24516641,Human_RBP_ID_27357844,Human_RBP_ID_27768662 RMVar_hsa_circ_116558,RMVar_hsa_circ_245017 54080 RMVar_ID_54080 Human_SNP_ID_868256617 A-to-I Human chr7 - 121441196 121441196 121441196 AGCCACCTCTGTCCCTTTCCCGGATGATCCCGAAAATGAAGCTTCCTGGCCAGGAAAACAAAACG AGCCACCTCTGTCCCTTTCCCGGATGATCCCGCAAATGAAGCTTCCTGGCCAGGAAAACAAAACG T G AC074085.2 Ensembl:ENSG00000234985 Pseudogene exon GSE100210 HepG2 cell line chr7:121441195..121441196 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA 33..33 33 UCEC 1 - Human_RBP_ID_18090841 54081 RMVar_ID_54081 Human_SNP_ID_868256622 A-to-I Human chr7 - 121441196 121441196 121441196 AGCCACCTCTGTCCCTTTCCCGGATGATCCCGAAAATGAAGCTTCCTGGCCAGGAAAACAAAACG AGCCACCTCTGTCCCTTTCCCGGATGATCCCGGAAATGAAGCTTCCTGGCCAGGAAAACAAAACG T C AC074085.2 Ensembl:ENSG00000234985 Pseudogene exon GSE100210 HepG2 cell line chr7:121441195..121441196 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA 33..33 33 UCEC 1 - Human_RBP_ID_18090841 54082 RMVar_ID_54082 Human_SNP_ID_868294779 A-to-I Human chr7 - 56049955 56049955 56049955 GAGGTGGGCGGATCACTTGAGGTCAGGAGTTCAAGACCATCCTGGCCAACATGGTGAAACCCCGT GAGGTGGGCGGATCACTTGAGGTCAGGAGTTCGAGACCATCCTGGCCAACATGGTGAAACCCCGT T C PSPH Ensembl:ENSG00000146733 Protein coding intron GSE38233 cultured B-cells chr7:56049954..56049955 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 54083 RMVar_ID_54083 Human_SNP_ID_868302727 A-to-I Human chr7 - 100352795 100352795 100352795 CGCAGGGGCTGCTGGCCCCAGAGCCTTCCAGGATGAGAGAGATGCTGCTCTGGGTTTCCCAGCGG CGCAGGGGCTGCTGGCCCCAGAGCCTTCCAGGGTGAGAGAGATGCTGCTCTGGGTTTCCCAGCGG T C - - Other Unknown GSE107867 ASD brains,cerebellum;ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr7:100352794..100352795 30559470 RNA-Seq:(High) rs559354079 Functional Loss SNV COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 2 brain 54084 RMVar_ID_54084 Human_SNP_ID_868311449 A-to-I Human chr7 - 135129311 135129311 135129311 TCTATTAATTTCTCTGCAGTCACCTTACATGGAGAGACCCCATGGTAGGTCAACCTGCACAAGGT TCTATTAATTTCTCTGCAGTCACCTTACATGGGGAGACCCCATGGTAGGTCAACCTGCACAAGGT T C CYREN Ensembl:ENSG00000122783 Protein coding intron GSE100210 HepG2 cell line chr7:135129310..135129311 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue 54085 RMVar_ID_54085 Human_SNP_ID_868368388 A-to-I Human chr7 + 38221377 38221377 38221377 GTCTAATCACTCCTCCATTACATCCATTTTTTATAAGTCTGTGTCTTACCACTAATCTCTTGTAA GTCTAATCACTCCTCCATTACATCCATTTTTTGTAAGTCTGTGTCTTACCACTAATCTCTTGTAA A G STARD3NL Ensembl:ENSG00000010270 Protein coding intron GSE47997 K562 cells&HepG2 cells chr7:38221376..38221377 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 4 prostate RMVar_hsa_circ_96400,RMVar_hsa_circ_301869,RMVar_hsa_circ_244699 54086 RMVar_ID_54086 Human_SNP_ID_868393793 A-to-I Human chr7 - 16089446 16089418 16089447 ATGTACGTACATATATACACATATATGTATGCACGTACATATATACACATATATGTATGTACGTA ATGTACGTACATATATACACATATATGTATG_____________________________ACGTA TACATACATATATGTGTATATATGTACGTG T CRPPA Ensembl:ENSG00000214960 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells chr7:16089445..16089446 23474544 RNA-Seq:(High) - Functional Loss DEL ICGC 32..60 33 SKCA 1 - Human_RBP_ID_17578351 RMVar_hsa_circ_112717,RMVar_hsa_circ_116458,RMVar_hsa_circ_243875,RMVar_hsa_circ_243876 54087 RMVar_ID_54087 Human_SNP_ID_868395316 A-to-I Human chr7 + 39950745 39950745 39950745 ACGCCGCAAGCGGAGGCGATTCCTGTCCCCTCAGCAGCCGCCGCTGCTGTTGCCGCTCCTGCAGC ACGCCGCAAGCGGAGGCGATTCCTGTCCCCTCGGCAGCCGCCGCTGCTGTTGCCGCTCCTGCAGC A G CDK13 Ensembl:ENSG00000065883 Protein coding CDS GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line chr7:39950744..39950745 29129909,32596459,32596459 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_956844,Human_RBP_ID_26102630 Human_miRNA_ID_2756335 RMVar_hsa_circ_115465,RMVar_hsa_circ_244746 54088 RMVar_ID_54088 Human_SNP_ID_868521404 A-to-I Human chr7 - 42926323 42926323 42926323 AAAGAGAATAACTCAGATGTGAAAGAGGAGGTAGATAGATTACATAACTCCTCTTTTCTCTGTTC AAAGAGAATAACTCAGATGTGAAAGAGGAGGTGGATAGATTACATAACTCCTCTTTTCTCTGTTC T C PSMA2,AC010132.3 Ensembl:ENSG00000106588,Ensembl:ENSG00000256646 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line chr7:42926322..42926323 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 CHOL 1 - RMVar_hsa_circ_5340,RMVar_hsa_circ_50200 54089 RMVar_ID_54089 Human_SNP_ID_868554063 A-to-I Human chr7 + 66746710 66746710 66746710 TGGTGGCACGATCTCTACTCACTGCAACTTCCACCTCCCCGGTTCAAGCGATTCTTGTGCCTCAG TGGTGGCACGATCTCTACTCACTGCAACTTCCCCCTCCCCGGTTCAAGCGATTCTTGTGCCTCAG A C AC027644.4,RABGEF1 Ensembl:ENSG00000284461,Ensembl:ENSG00000154710 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line chr7:66746709..66746710 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - RMVar_hsa_circ_112691,RMVar_hsa_circ_245367,RMVar_hsa_circ_18303,RMVar_hsa_circ_245369,RMVar_hsa_circ_80384 54090 RMVar_ID_54090 Human_SNP_ID_868612980 A-to-I Human chr7 - 5499648 5499648 5499648 TGGTTCATTGCAACCCCTGCCTCCTGGGTTCAAGCGATTCTCCCACCTCAGCCTCCCGAGCAGCT TGGTTCATTGCAACCCCTGCCTCCTGGGTTCATGCGATTCTCCCACCTCAGCCTCCCGAGCAGCT T A FBXL18 Ensembl:ENSG00000155034 Protein coding intron GSE38233 cultured B-cells chr7:5499647..5499648 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - RMVar_hsa_circ_277673,RMVar_hsa_circ_243501 54091 RMVar_ID_54091 Human_SNP_ID_868624957 A-to-I Human chr7 + 74534620 74534620 74534620 ATGGGAGGCAGAGCTGGGGGAGCGAGGCTGACAATGACTCCTGTTTTCACGCTGAGAGACCCCAC ATGGGAGGCAGAGCTGGGGGAGCGAGGCTGACGATGACTCCTGTTTTCACGCTGAGAGACCCCAC A G GTF2IRD1 Ensembl:ENSG00000006704 Protein coding intron GSE100210 HepG2 cell line chr7:74534620..74534621 29129909 RNA-Seq:(High) rs73135381 Functional Loss SNV ICGC 33..33 33 LAML 1 - GWAS_ID_3421,GWAS_ID_3422,GWAS_ID_3423,GWAS_ID_3424,GWAS_ID_3425,GWAS_ID_3426,GWAS_ID_3427,GWAS_ID_3428,GWAS_ID_3429,GWAS_ID_3430,GWAS_ID_3431,GWAS_ID_3432,GWAS_ID_3433,GWAS_ID_3434,GWAS_ID_3435,GWAS_ID_3436 RMVar_hsa_circ_10311,RMVar_hsa_circ_324396,RMVar_hsa_circ_370080,RMVar_hsa_circ_296453,RMVar_hsa_circ_29785,RMVar_hsa_circ_267507,RMVar_hsa_circ_13882,RMVar_hsa_circ_245704,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_245711 54092 RMVar_ID_54092 Human_SNP_ID_868629065 A-to-I Human chr7 - 76039804 76039804 76039804 CGTCTCTATAAAAATACAAAAATTAGCCTGTCATGGTGGTGCATGCCTGTAGTCCTTGCTACTGG CGTCTCTATAAAAATACAAAAATTAGCCTGTCGTGGTGGTGCATGCCTGTAGTCCTTGCTACTGG T C STYXL1 Ensembl:ENSG00000127952 Protein coding intron GSE38233 cultured B-cells chr7:76039803..76039804 24183664 RNA-Seq:(High) rs576731139 Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_10360951 Human_miRNA_ID_2753433,Human_miRNA_ID_2753434,Human_miRNA_ID_2755367,Human_miRNA_ID_2755368 RMVar_hsa_circ_245793,RMVar_hsa_circ_83205 54093 RMVar_ID_54093 Human_SNP_ID_868631863 A-to-I Human chr7 - 6470733 6470733 6470733 TCCGTGCATGATGGTGGTCATAGTGGTGGCGGATTAAATCAAGAAGTATATGTTTACAAACAAAA TCCGTGCATGATGGTGGTCATAGTGGTGGCGGGTTAAATCAAGAAGTATATGTTTACAAACAAAA T C KDELR2,DAGLB Ensembl:ENSG00000136240,Ensembl:ENSG00000164535 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells chr7:6470732..6470733 24183664 RNA-Seq:(High) rs58885063 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_3097202,Human_RBP_ID_16191821,Human_RBP_ID_17577103 Human_miRNA_ID_2343729 RMVar_hsa_circ_91785,RMVar_hsa_circ_243659,RMVar_hsa_circ_120377,RMVar_hsa_circ_243668,RMVar_hsa_circ_316068,RMVar_hsa_circ_271617,RMVar_hsa_circ_243672 54094 RMVar_ID_54094 Human_SNP_ID_868651501 A-to-I Human chr7 + 42919359 42919359 42919359 TGACCCTGGCTCATAAACACATTATCAAGACTATGGATTTCATGCAGGATAGTAATTATTTGTTA TGACCCTGGCTCATAAACACATTATCAAGACTGTGGATTTCATGCAGGATAGTAATTATTTGTTA A G AC010132.2 Ensembl:ENSG00000234983 Pseudogene exon GSE100210 HepG2 cell line chr7:42919358..42919359 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 lung squamous_cell_carcinoma 2 lung 54095 RMVar_ID_54095 Human_SNP_ID_868695567 A-to-I Human chr7 - 75999112 75999112 75999112 TTTTTTTGAGACGGAGTCTCGCTCTGTCACCCAGGCTGGAGTACAGTAGCACAATCTCGACTCAC TTTTTTTGAGACGGAGTCTCGCTCTGTCACCCTGGCTGGAGTACAGTAGCACAATCTCGACTCAC T A STYXL1 Ensembl:ENSG00000127952 Protein coding intron GSE47997 K562 cells&HepG2 cells chr7:75999111..75999112 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_Splice_Rec_879282 RMVar_hsa_circ_245781,RMVar_hsa_circ_100654,RMVar_hsa_circ_245782,RMVar_hsa_circ_245783,RMVar_hsa_circ_376920 54096 RMVar_ID_54096 Human_SNP_ID_868738431 A-to-I Human chr7 - 44580234 44580234 44580234 GCCTCAGGCAATCCACTGCCGCAGCCTCCCAAAGTGTTGGGATTACAGGCGTGAGCCACTGCACC GCCTCAGGCAATCCACTGCCGCAGCCTCCCAACGTGTTGGGATTACAGGCGTGAGCCACTGCACC T G TMED4 Ensembl:ENSG00000158604 Protein coding intron GSE100210 HepG2 cell line chr7:44580233..44580234 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ER-HER-positive_carcinoma,breast HER-positive_carcinoma 7 breast Human_RBP_ID_9211365,Human_RBP_ID_23077065,Human_RBP_ID_26138063 54097 RMVar_ID_54097 Human_SNP_ID_868757030 A-to-I Human chr7 + 4787289 4787289 4787289 CCAAGGCAGGAGGATCTTGAGGCCAGGAGTTCAAGACCAGCCTGGGCAACACAGGGAGACCTCTT CCAAGGCAGGAGGATCTTGAGGCCAGGAGTTCGAGACCAGCCTGGGCAACACAGGGAGACCTCTT A G AP5Z1 Ensembl:ENSG00000242802 Protein coding intron GSE38233 cultured B-cells chr7:4787288..4787289 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - RMVar_hsa_circ_82011,RMVar_hsa_circ_83973,RMVar_hsa_circ_243451,RMVar_hsa_circ_25547,RMVar_hsa_circ_243452 54098 RMVar_ID_54098 Human_SNP_ID_868761546 A-to-I Human chr7 + 56072065 56072065 56072065 AGGAGGTGGAGGTTGCAGTGAGCTGAGATTGCACCACTGCACTCCAGCCTGGGCAACAGTCTTTT AGGAGGTGGAGGTTGCAGTGAGCTGAGATTGCGCCACTGCACTCCAGCCTGGGCAACAGTCTTTT A G SUMF2 Ensembl:ENSG00000129103 Protein coding intron GSE100210 HepG2 cell line chr7:56072064..56072065 29129909 RNA-Seq:(High) rs1297240725 Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 9 haematopoietic and lymphoid tissue Human_RBP_ID_22011830 RMVar_hsa_circ_65684,RMVar_hsa_circ_95157,RMVar_hsa_circ_245233,RMVar_hsa_circ_272731,RMVar_hsa_circ_245234 54099 RMVar_ID_54099 Human_SNP_ID_868763596 A-to-I Human chr7 + 127738476 127738476 127738476 AATTTTTTGCATTTTTAGTAGAGAGGGGTTTCACCACGTTGGCCAGGCTGGTCTTGAACTCCTGA AATTTTTTGCATTTTTAGTAGAGAGGGGTTTCGCCACGTTGGCCAGGCTGGTCTTGAACTCCTGA A G SND1 Ensembl:ENSG00000197157 Protein coding intron GSE100210 HepG2 cell line chr7:127738475..127738476 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 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 54100 RMVar_ID_54100 Human_SNP_ID_868885691 A-to-I Human chr7 + 139534262 139534262 139534262 AGTTTGGCGCGATGTCTCACACCATTTTGCTGATACAGACTACCAAGAGGCCAGAAGGCAGAACT AGTTTGGCGCGATGTCTCACACCATTTTGCTGGTACAGACTACCAAGAGGCCAGAAGGCAGAACT A G CLEC2L,ERHP1 Ensembl:ENSG00000236279,Ensembl:ENSG00000254270 Protein coding,Pseudogene intron,exon GSE38233 cultured B-cells chr7:139534261..139534262 24183664 RNA-Seq:(High) rs879035410 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue Human_miRNA_ID_1893793 54101 RMVar_ID_54101 Human_SNP_ID_868940324 A-to-I Human chr7 + 131427578 131427578 131427578 ACTTTTTTTTTATTTTTCATTTTTTGAGACAGAGTCTCACACTGTCACCCCAGGCTGGAGTGCAG ACTTTTTTTTTATTTTTCATTTTTTGAGACAGGGTCTCACACTGTCACCCCAGGCTGGAGTGCAG A G MKLN1 Ensembl:ENSG00000128585 Protein coding intron GSE100210 HepG2 cell line chr7:131427577..131427578 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_23315698 RMVar_hsa_circ_596,RMVar_hsa_circ_114367,RMVar_hsa_circ_248512,RMVar_hsa_circ_319018,RMVar_hsa_circ_126807,RMVar_hsa_circ_368252,RMVar_hsa_circ_248514,RMVar_hsa_circ_347651,RMVar_hsa_circ_365577,RMVar_hsa_circ_298980,RMVar_hsa_circ_303813,RMVar_hsa_circ_13998,RMVar_hsa_circ_62622,RMVar_hsa_circ_248525,RMVar_hsa_circ_248526,RMVar_hsa_circ_285702,RMVar_hsa_circ_343168,RMVar_hsa_circ_295320,RMVar_hsa_circ_110742,RMVar_hsa_circ_71912,RMVar_hsa_circ_17649,RMVar_hsa_circ_248527,RMVar_hsa_circ_51462,RMVar_hsa_circ_248529,RMVar_hsa_circ_248530,RMVar_hsa_circ_248528,RMVar_hsa_circ_12446,RMVar_hsa_circ_120803,RMVar_hsa_circ_33321,RMVar_hsa_circ_60460,RMVar_hsa_circ_248541,RMVar_hsa_circ_268832,RMVar_hsa_circ_34192,RMVar_hsa_circ_280059,RMVar_hsa_circ_322679,RMVar_hsa_circ_353415,RMVar_hsa_circ_37773,RMVar_hsa_circ_248542,RMVar_hsa_circ_27891,RMVar_hsa_circ_277531,RMVar_hsa_circ_349320,RMVar_hsa_circ_370623,RMVar_hsa_circ_64955,RMVar_hsa_circ_248543 54102 RMVar_ID_54102 Human_SNP_ID_869041970 A-to-I Human chr7 + 99341548 99341548 99341548 GGAGAATTGCTTGAACCTGGGAGGCGGAGGTTACGGTGAGCCGAGATTGTGCCATTGCACGCCAG GGAGAATTGCTTGAACCTGGGAGGCGGAGGTTGCGGTGAGCCGAGATTGTGCCATTGCACGCCAG A G AC004922.1,ARPC1A Ensembl:ENSG00000284292,Ensembl:ENSG00000241685 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line chr7:99341547..99341548 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_15222,RMVar_hsa_circ_290462,RMVar_hsa_circ_312112,RMVar_hsa_circ_374284,RMVar_hsa_circ_291744,RMVar_hsa_circ_90807,RMVar_hsa_circ_89831,RMVar_hsa_circ_98173,RMVar_hsa_circ_246916,RMVar_hsa_circ_246918,RMVar_hsa_circ_246919,RMVar_hsa_circ_246920,RMVar_hsa_circ_246917,RMVar_hsa_circ_345008,RMVar_hsa_circ_315932,RMVar_hsa_circ_55242,RMVar_hsa_circ_246922,RMVar_hsa_circ_19323,RMVar_hsa_circ_246921 54103 RMVar_ID_54103 Human_SNP_ID_869065486 A-to-I Human chr7 - 129924206 129924206 129924206 GTGAAAGTATAATTTTAAACAAATGTTTTTGTAGAGACAGGGTCTCACTATATTGCCCAGGCTGA GTGAAAGTATAATTTTAAACAAATGTTTTTGTGGAGACAGGGTCTCACTATATTGCCCAGGCTGA T C UBE2H Ensembl:ENSG00000186591 Protein coding intron GSE100210 HepG2 cell line chr7:129924205..129924206 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 54104 RMVar_ID_54104 Human_SNP_ID_869070747 A-to-I Human chr7 - 6244589 6244589 6244589 GTGATGGTGTATACTGGTAGTCCCAGCTACTCAGGAGGCTGAGGCAGGAGGATCGCTTGAGTCCA GTGATGGTGTATACTGGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGGATCGCTTGAGTCCA T C CYTH3 Ensembl:ENSG00000008256 Protein coding intron GSE100210 HepG2 cell line chr7:6244588..6244589 29129909 RNA-Seq:(High) rs1253166120 Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 3 oesophagus 54105 RMVar_ID_54105 Human_SNP_ID_869078167 A-to-I Human chr7 + 6747535 6747535 6747535 GAGTTCAGGAGATCGAGACCATCCTGGCTAACATGGTGAAAGCCCGTCTCTACTAAAAATACAAA GAGTTCAGGAGATCGAGACCATCCTGGCTAACGTGGTGAAAGCCCGTCTCTACTAAAAATACAAA A G PMS2CL Ensembl:ENSG00000187953 Pseudogene intron GSE47997 K562 cells&HepG2 cells chr7:6747534..6747535 23474544 RNA-Seq:(High) rs867139250 Functional Loss SNV ICGC 33..33 33 PBCA 1 - 54106 RMVar_ID_54106 Human_SNP_ID_869078276 A-to-I Human chr7 - 67304085 67304085 67304085 GTGGTGGCGTGCACCTGTAATCCAAGCTACTCAGGAGGCTGAGATGGGAGAACTGCTTGAACCCG GTGGTGGCGTGCACCTGTAATCCAAGCTACTCGGGAGGCTGAGATGGGAGAACTGCTTGAACCCG T C RF00017-1020 RNACentral:URS000099BA6B SRP RNA intron GSE100210 HepG2 cell line chr7:67304084..67304085 29129909 RNA-Seq:(High) rs374389376 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 54107 RMVar_ID_54107 Human_SNP_ID_869087799 A-to-I Human chr7 - 150749954 150749954 150749954 TTGCCCATAGTTTTACCTAGAAATCCAGTTGTAGAATCAAATTGTGAATCCATTACAGCTAATAA TTGCCCATAGTTTTACCTAGAAATCCAGTTGTTGAATCAAATTGTGAATCCATTACAGCTAATAA T A - - Other Unknown GSE100210 HepG2 cell line chr7:150749953..150749954 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA 33..33 33 LUAD 1 - 54108 RMVar_ID_54108 Human_SNP_ID_869087806 A-to-I Human chr7 - 150749954 150749954 150749954 TTGCCCATAGTTTTACCTAGAAATCCAGTTGTAGAATCAAATTGTGAATCCATTACAGCTAATAA TTGCCCATAGTTTTACCTAGAAATCCAGTTGTGGAATCAAATTGTGAATCCATTACAGCTAATAA T C - - Other Unknown GSE100210 HepG2 cell line chr7:150749953..150749954 29129909 RNA-Seq:(High) rs879214954 Functional Loss SNV ICGC 33..33 33 LAML 1 - 54109 RMVar_ID_54109 Human_SNP_ID_869090910 A-to-I Human chr7 + 70139214 70139214 70139214 GTCTTGAACTCCTGGGCTCAAGCTATCTACCCACCTTGGCCTCCCAAAGTGCTAAGATTACAGGC GTCTTGAACTCCTGGGCTCAAGCTATCTACCCGCCTTGGCCTCCCAAAGTGCTAAGATTACAGGC A G AUTS2 Ensembl:ENSG00000158321 Protein coding intron GSE107867 ASD brains,cerebellum chr7:70139213..70139214 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_119594,RMVar_hsa_circ_245462,RMVar_hsa_circ_75596,RMVar_hsa_circ_245461,RMVar_hsa_circ_124120,RMVar_hsa_circ_122595,RMVar_hsa_circ_245472,RMVar_hsa_circ_245473,RMVar_hsa_circ_245474 54110 RMVar_ID_54110 Human_SNP_ID_869139344 A-to-I Human chr7 + 87161363 87161363 87161363 CTACTAAAAAAATACCAAAAAATTAGCTGGGCATGGTGGCACACGCCTGTAGTCCCAGCTACTCA CTACTAAAAAAATACCAAAAAATTAGCTGGGCGTGGTGGCACACGCCTGTAGTCCCAGCTACTCA A G DMTF1 Ensembl:ENSG00000135164 Protein coding intron GSE100210 HepG2 cell line chr7:87161362..87161363 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 STAD 1 - RMVar_hsa_circ_313994,RMVar_hsa_circ_340846,RMVar_hsa_circ_246234 54111 RMVar_ID_54111 Human_SNP_ID_869159139 A-to-I Human chr7 - 100220138 100220138 100220138 TGAAGGACGAGAGCTCGGTGGCCTCCATCCGAACTTGAACCCACACCTCCGGGGTCCCTGTGGAA TGAAGGACGAGAGCTCGGTGGCCTCCATCCGAGCTTGAACCCACACCTCCGGGGTCCCTGTGGAA T C CASTOR3 Ensembl:ENSG00000239521 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank chr7:100220137..100220138 30559470 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 bile_duct adenocarcinoma,biliary_tract adenocarcinoma 3 biliary tract,gallbladder Human_RBP_ID_26765035 RMVar_hsa_circ_88038,RMVar_hsa_circ_247081 54112 RMVar_ID_54112 Human_SNP_ID_869180227 A-to-I Human chr7 + 74178360 74178360 74178360 TCACTTGTGGCCAGAAGTTTGAGACCACCCTGACCAACGTGGCAAAACCCCATGTCTACTAAAAA TCACTTGTGGCCAGAAGTTTGAGACCACCCTGGCCAACGTGGCAAAACCCCATGTCTACTAAAAA A G EIF4H Ensembl:ENSG00000106682 Protein coding intron GSE38233 cultured B-cells chr7:74178359..74178360 24183664 RNA-Seq:(High) rs150878 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 3 large intestine GWAS_ID_3414,GWAS_ID_3415,GWAS_ID_3416,GWAS_ID_3417,GWAS_ID_3418,GWAS_ID_3419,GWAS_ID_3420 RMVar_hsa_circ_99960,RMVar_hsa_circ_245630 54113 RMVar_ID_54113 Human_SNP_ID_869198275 A-to-I Human chr7 + 100352794 100352794 100352794 CCCGCTGGGAAACCCAGAGCAGCATCTCTCTCATCCTGGAAGGCTCTGGGGCCAGCAGCCCCTGC CCCGCTGGGAAACCCAGAGCAGCATCTCTCTCGTCCTGGAAGGCTCTGGGGCCAGCAGCCCCTGC A G PILRB,STAG3L5P-PVRIG2P-PILRB,PVRIG2P Ensembl:ENSG00000121716,Ensembl:ENSG00000272752,Ensembl:ENSG00000235333 Protein coding,lincRNA,Pseudogene 5'UTR,exon,exon GSE107867 ASD brains,cerebellum;ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr7:100352793..100352794 30559470 RNA-Seq:(High) rs547186306 Functional Loss SNV COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,brain astrocytoma_Grade_IV 2 brain Human_RBP_ID_17430162 Human_Splice_Rec_898670,Human_Splice_Rec_898812 RMVar_hsa_circ_48532,RMVar_hsa_circ_93853,RMVar_hsa_circ_77737,RMVar_hsa_circ_247091,RMVar_hsa_circ_247092 54114 RMVar_ID_54114 Human_SNP_ID_869201573 A-to-I Human chr7 - 75492903 75492903 75492903 TGTTCCAACTACTTGGGAGACTCGTGACAGGAAGATCACTTGAGCCCAGGAGTTAGAAGCTGCAG TGTTCCAACTACTTGGGAGACTCGTGACAGGACGATCACTTGAGCCCAGGAGTTAGAAGCTGCAG T G RF00017-4673 RNACentral:URS000091B0E9 SRP RNA intron GSE100210 HepG2 cell line chr7:75492902..75492903 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 NKTL 1 - 54115 RMVar_ID_54115 Human_SNP_ID_869222578 A-to-I Human chr7 - 135972760 135972760 135972760 GCAATGAGAAATCACAAAAGTATTAATATTTTAAGGGCAGTGAGGGAGACTGGCTGAAAAAGATT GCAATGAGAAATCACAAAAGTATTAATATTTTGAGGGCAGTGAGGGAGACTGGCTGAAAAAGATT T C MTPN Ensembl:ENSG00000105887 Protein coding intron GSE100210 HepG2 cell line chr7:135972759..135972760 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_17577968 RMVar_hsa_circ_119289,RMVar_hsa_circ_248782,RMVar_hsa_circ_248784 54116 RMVar_ID_54116 Human_SNP_ID_869255123 A-to-I Human chr7 - 65747995 65747995 65747995 AAAAAAAGCCTGGTGTGGTGGCGCACACCTGTAATCCCAGCTACTTAGGTGGCTGAGGCAGAATT AAAAAAAGCCTGGTGTGGTGGCGCACACCTGTGATCCCAGCTACTTAGGTGGCTGAGGCAGAATT T C AC073107.1 Ensembl:ENSG00000272693 Pseudogene intron GSE100210 HepG2 cell line chr7:65747994..65747995 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_17429768 54117 RMVar_ID_54117 Human_SNP_ID_869283257 A-to-I Human chr7 - 5977258 5977258 5977258 GAGTTCAGGAGATCGAGACCATCCTGGCTAACATGGTGAAAGCCCGTCTCTACTAAAAATACAAA GAGTTCAGGAGATCGAGACCATCCTGGCTAACGTGGTGAAAGCCCGTCTCTACTAAAAATACAAA T C PMS2 Ensembl:ENSG00000122512 Protein coding intron GSE47997 K562 cells&HepG2 cells chr7:5977257..5977258 23474544 RNA-Seq:(High) rs188558508 Functional Loss SNV ICGC 33..33 33 LAML 1 - 54118 RMVar_ID_54118 Human_SNP_ID_869285674 A-to-I Human chr7 + 99518167 99518167 99518167 GTGCAAACTAGGGGCCAGGCACAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCATTGC GTGCAAACTAGGGGCCAGGCACAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCATTGC A G ZKSCAN5 Ensembl:ENSG00000196652 Protein coding intron GSE100210 HepG2 cell line chr7:99518166..99518167 29129909 RNA-Seq:(High) rs948188667 Functional Loss SNV ICGC 33..33 33 PAAD 1 - RMVar_hsa_circ_366409 54119 RMVar_ID_54119 Human_SNP_ID_869304080 A-to-I Human chr7 + 100149880 100149880 100149880 TCACTGCAACCTCCGCCTCCGGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGA TCACTGCAACCTCCGCCTCCGGGGTTCAAGCGCTTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGA A C LAMTOR4 Ensembl:ENSG00000188186 Protein coding intron GSE38233 cultured B-cells chr7:100149879..100149880 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 8 pancreas RMVar_hsa_circ_247066,RMVar_hsa_circ_76464,RMVar_hsa_circ_247065 54120 RMVar_ID_54120 Human_SNP_ID_869310934 A-to-I Human chr7 + 44467976 44467976 44467976 AACCAAGAAGTTCATCCAGCACCAGTCAGACCAATATGTCAAAATTAAGCGTAACTGGCGGAAAC AACCAAGAAGTTCATCCAGCACCAGTCAGACCGATATGTCAAAATTAAGCGTAACTGGCGGAAAC A G AC004453.1 Ensembl:ENSG00000146677 Pseudogene exon GSE100210 HepG2 cell line chr7:44467975..44467976 29129909 RNA-Seq:(High) rs533465480 Functional Loss SNV ICGC,COSMIC 33..33 33 breast ductal_carcinoma,LAML,oesophagus adenocarcinoma,large_intestine adenocarcinoma,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 8 oesophagus,large intestine,haematopoietic and lymphoid tissue,breast Human_RBP_ID_684637,Human_RBP_ID_1052116,Human_RBP_ID_9211327,Human_RBP_ID_17316391,Human_RBP_ID_18520218,Human_RBP_ID_24216503,Human_RBP_ID_26552290,Human_RBP_ID_27113864 54121 RMVar_ID_54121 Human_SNP_ID_869352000 A-to-I Human chr7 - 148814106 148814106 148814106 GGTCAAAACCGCTTTCCGGGATGCCGCTGCAAAGCACAGTGCAACACCAAGCAGTGCCCGTGCTA GGTCAAAACCGCTTTCCGGGATGCCGCTGCAATGCACAGTGCAACACCAAGCAGTGCCCGTGCTA T A EZH2 Ensembl:ENSG00000106462 Protein coding 3'UTR GSE100210 HepG2 cell line chr7:148814105..148814106 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 OV,ovary serous_carcinoma 8 ovary Human_RBP_ID_1683153,Human_RBP_ID_18877832 Human_Splice_Rec_935068,Human_Splice_Rec_935106,Human_Splice_Rec_935144,Human_Splice_Rec_935182,Human_Splice_Rec_935218,Human_Splice_Rec_935254,Human_Splice_Rec_935292 Human_miRNA_ID_1312630,Human_miRNA_ID_2236739 RMVar_hsa_circ_52291,RMVar_hsa_circ_327932,RMVar_hsa_circ_50935,RMVar_hsa_circ_354172,RMVar_hsa_circ_87944,RMVar_hsa_circ_317883,RMVar_hsa_circ_371414,RMVar_hsa_circ_82698,RMVar_hsa_circ_249303,RMVar_hsa_circ_249305,RMVar_hsa_circ_23554,RMVar_hsa_circ_249304 54122 RMVar_ID_54122 Human_SNP_ID_869354717 A-to-I Human chr7 + 66121138 66121138 66121138 CTCTTGTCACCCAGGCTGGAGTGCAATGGCGCAATCTCGGCTGACTGCAACCTCCGCCTCCCGAG CTCTTGTCACCCAGGCTGGAGTGCAATGGCGCTATCTCGGCTGACTGCAACCTCCGCCTCCCGAG A T CRCP,AC068533.4 Ensembl:ENSG00000241258,Ensembl:ENSG00000249319 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line chr7:66121137..66121138 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_245326,RMVar_hsa_circ_109892 54123 RMVar_ID_54123 Human_SNP_ID_869366035 A-to-I Human chr7 + 56079014 56079014 56079014 AAACTGCCAGGCTCTAGCGATTCTTCCACCTCAGCTCCTCAAGTATCTGGGACTACAGGTGCGGC AAACTGCCAGGCTCTAGCGATTCTTCCACCTCGGCTCCTCAAGTATCTGGGACTACAGGTGCGGC A G SUMF2 Ensembl:ENSG00000129103 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr7:56079013..56079014 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 8 haematopoietic and lymphoid tissue Human_Splice_Rec_869216,Human_Splice_Rec_869217 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 54124 RMVar_ID_54124 Human_SNP_ID_869422129 A-to-I Human chr7 + 87897823 87897823 87897823 TTGAGATGGAGTCTTGCTCTGTCACCCAGGCTAGAGTGCAGTGGCACGATCTCGGCTCACTGCAA TTGAGATGGAGTCTTGCTCTGTCACCCAGGCTGGAGTGCAGTGGCACGATCTCGGCTCACTGCAA A G DBF4 Ensembl:ENSG00000006634 Protein coding intron GSE38233 cultured B-cells chr7:87897822..87897823 24183664 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 1 prostate RMVar_hsa_circ_10076 54125 RMVar_ID_54125 Human_SNP_ID_869426181 A-to-I Human chr7 - 47559187 47559187 47559187 CGTCACCATGCCTGGCTAATTTCTGTATTTTTAGTAGAGATGGAGTTTCACCATATTGGCCAGAC CGTCACCATGCCTGGCTAATTTCTGTATTTTTTGTAGAGATGGAGTTTCACCATATTGGCCAGAC T A TNS3 Ensembl:ENSG00000136205 Protein coding intron GSE100210 HepG2 cell line chr7:47559186..47559187 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_124921,RMVar_hsa_circ_245088,RMVar_hsa_circ_127348,RMVar_hsa_circ_245102 54126 RMVar_ID_54126 Human_SNP_ID_869437286 A-to-I Human chr7 + 66142680 66142680 66142680 GCTTGGCTAATTGTTTTATTTTTATTTTTTGTAAAGACAGAGTCTCACTTTGTTGCCCAGGCTGT GCTTGGCTAATTGTTTTATTTTTATTTTTTGTGAAGACAGAGTCTCACTTTGTTGCCCAGGCTGT A G CRCP,AC068533.4 Ensembl:ENSG00000241258,Ensembl:ENSG00000249319 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line chr7:66142680..66142681 29129909 RNA-Seq:(High) rs1049012005 Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_273218,RMVar_hsa_circ_245330,RMVar_hsa_circ_302999,RMVar_hsa_circ_245334,RMVar_hsa_circ_245335 54127 RMVar_ID_54127 Human_SNP_ID_869473854 A-to-I Human chr7 + 66775310 66775310 66775310 GGCCCAATCCCTCACATTCTCCAAGTTTGAAGAAAAGAAAACCAACGAGAAGACCCGCAAGGTTA GGCCCAATCCCTCACATTCTCCAAGTTTGAAGGAAAGAAAACCAACGAGAAGACCCGCAAGGTTA A G AC027644.4,RABGEF1 Ensembl:ENSG00000284461,Ensembl:ENSG00000154710 Protein coding,Protein coding 3'UTR,CDS GSE107867 ASD brains,frontal_cortex chr7:66775309..66775310 30559470 RNA-Seq:(High) rs778572706 Functional Loss SNV ICGC,COSMIC 33..33 33 rectum adenocarcinoma,LICA,liver neoplasm,large_intestine adenocarcinoma,endometrium endometrioid_carcinoma 19 uterus,liver,large intestine Human_RBP_ID_8271961,Human_RBP_ID_9403397,Human_RBP_ID_24549111 Human_Splice_Rec_871476,Human_Splice_Rec_871477,Human_Splice_Rec_871530,Human_Splice_Rec_871531,Human_Splice_Rec_871544,Human_Splice_Rec_871545,Human_Splice_Rec_871558,Human_Splice_Rec_871576,Human_Splice_Rec_871577,Human_Splice_Rec_871592,Human_Splice_Rec_871593,Human_Splice_Rec_871608,Human_Splice_Rec_871609,Human_Splice_Rec_871624,Human_Splice_Rec_871625,Human_Splice_Rec_871640,Human_Splice_Rec_871641 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_245373,RMVar_hsa_circ_245377,RMVar_hsa_circ_293552,RMVar_hsa_circ_245371,RMVar_hsa_circ_12986,RMVar_hsa_circ_320004,RMVar_hsa_circ_377698,RMVar_hsa_circ_300161,RMVar_hsa_circ_278920,RMVar_hsa_circ_284379,RMVar_hsa_circ_273398,RMVar_hsa_circ_245375,RMVar_hsa_circ_245376,RMVar_hsa_circ_245374,RMVar_hsa_circ_245380,RMVar_hsa_circ_306660,RMVar_hsa_circ_245378,RMVar_hsa_circ_245372,RMVar_hsa_circ_377787,RMVar_hsa_circ_319250,RMVar_hsa_circ_378697,RMVar_hsa_circ_274362,RMVar_hsa_circ_306573,RMVar_hsa_circ_245381,RMVar_hsa_circ_245379 54128 RMVar_ID_54128 Human_SNP_ID_869491303 A-to-I Human chr7 - 5721521 5721521 5721521 AATTGCGGACATACATTCACCAACAAATGGCTATAAGCAGCGCTATTCAGATTAACCCAAAACAG AATTGCGGACATACATTCACCAACAAATGGCTGTAAGCAGCGCTATTCAGATTAACCCAAAACAG T C RNF216 Ensembl:ENSG00000011275 Protein coding intron GSE38233 cultured B-cells chr7:5721520..5721521 24183664 RNA-Seq:(High) rs1990836 Functional Loss SNV ICGC 33..33 33 LAML 1 - GWAS_ID_5799,GWAS_ID_5800,GWAS_ID_5801,GWAS_ID_5802,GWAS_ID_5803 RMVar_hsa_circ_5877,RMVar_hsa_circ_56221,RMVar_hsa_circ_355082,RMVar_hsa_circ_275751,RMVar_hsa_circ_72654,RMVar_hsa_circ_302691,RMVar_hsa_circ_82528,RMVar_hsa_circ_243529,RMVar_hsa_circ_17287,RMVar_hsa_circ_324998,RMVar_hsa_circ_243530,RMVar_hsa_circ_314667,RMVar_hsa_circ_107473,RMVar_hsa_circ_275621,RMVar_hsa_circ_243532,RMVar_hsa_circ_9787,RMVar_hsa_circ_243533,RMVar_hsa_circ_243531,RMVar_hsa_circ_283132,RMVar_hsa_circ_4557,RMVar_hsa_circ_288692,RMVar_hsa_circ_243537,RMVar_hsa_circ_342124,RMVar_hsa_circ_243539,RMVar_hsa_circ_347438,RMVar_hsa_circ_358070,RMVar_hsa_circ_315138 54129 RMVar_ID_54129 Human_SNP_ID_869508819 A-to-I Human chr7 + 31108239 31108239 31108239 AATGTTTCTGGAGAGGCTTTCAGAGTGGCTGGAAAAGGCTCTTGTTGCTGTAATTTAGAGAGGAG AATGTTTCTGGAGAGGCTTTCAGAGTGGCTGGGAAAGGCTCTTGTTGCTGTAATTTAGAGAGGAG A G ADCYAP1R1 Ensembl:ENSG00000078549 Protein coding 3'UTR GSE107867 ASD brains,frontal_cortex chr7:31108238..31108239 30559470 RNA-Seq:(High) rs1024745450 Functional Loss SNV ICGC,COSMIC 33..33 33 SKCA,haematopoietic_and_lymphoid_tissue chronic_lymphocytic_leukaemia-small_lymphocytic_lymphoma 4 haematopoietic and lymphoid tissue 54130 RMVar_ID_54130 Human_SNP_ID_869511456 A-to-I Human chr7 - 66606943 66606943 66606943 TAAGATCCTAGTCGTCCGAAAATCCATTGCCCATGTTCTCACAGTTATTAACCAGACTCAGAAAG TAAGATCCTAGTCGTCCGAAAATCCATTGCCCGTGTTCTCACAGTTATTAACCAGACTCAGAAAG T C RPL35P5 Ensembl:ENSG00000225573 Pseudogene exon GSE100210 HepG2 cell line chr7:66606942..66606943 29129909 RNA-Seq:(High) rs879063956 Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_miRNA_ID_1878072 54131 RMVar_ID_54131 Human_SNP_ID_869560117 A-to-I Human chr7 - 30510981 30510981 30510981 GGAGATCAAGACCAGCCATGGGCAATATGGCAAAACCCCATCTCTACAAAAAATACAAAAATTAG GGAGATCAAGACCAGCCATGGGCAATATGGCACAACCCCATCTCTACAAAAAATACAAAAATTAG T G AC005154.5 Ensembl:ENSG00000281039 Protein coding intron GSE100210 HepG2 cell line chr7:30510980..30510981 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 54132 RMVar_ID_54132 Human_SNP_ID_869587904 A-to-I Human chr7 + 56082641 56082640 56082641 AGTCCAAAGAGACAATGGAGATGATGGAACAGAAATGGCGCTCGGGCTGGGACTCCCCCAACATC AGTCCAAAGAGACAATGGAGATGATGGAACAG_AATGGCGCTCGGGCTGGGACTCCCCCAACATC GA G - - Other Unknown GSE100210 HepG2 cell line chr7:56082640..56082641;chr7:56082641..56082642 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 33..33 33 LICA 1 - 54133 RMVar_ID_54133 Human_SNP_ID_869600981 A-to-I Human chr7 + 105072658 105072658 105072658 GTATTTCACTTAACTGTTAAATGCTCATGCCTATAATCCCAGCACTTTGGGAGGCCGAGGTGGGC GTATTTCACTTAACTGTTAAATGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGTGGGC A G KMT2E Ensembl:ENSG00000005483 Protein coding intron GSE38233 cultured B-cells chr7:105072657..105072658 24183664 RNA-Seq:(High) rs555413371 Functional Loss SNV ICGC,COSMIC 33..33 33 prostate adenocarcinoma,LICA 5 prostate Human_RBP_ID_15960953,Human_RBP_ID_26055360 RMVar_hsa_circ_6704,RMVar_hsa_circ_118314,RMVar_hsa_circ_320297,RMVar_hsa_circ_312768,RMVar_hsa_circ_264827,RMVar_hsa_circ_118535,RMVar_hsa_circ_85463,RMVar_hsa_circ_62855,RMVar_hsa_circ_247513,RMVar_hsa_circ_247517,RMVar_hsa_circ_247515,RMVar_hsa_circ_247516,RMVar_hsa_circ_247514,RMVar_hsa_circ_247525,RMVar_hsa_circ_268874,RMVar_hsa_circ_297368,RMVar_hsa_circ_328971,RMVar_hsa_circ_60526,RMVar_hsa_circ_75002,RMVar_hsa_circ_247526,RMVar_hsa_circ_305843,RMVar_hsa_circ_336300,RMVar_hsa_circ_375891,RMVar_hsa_circ_307264,RMVar_hsa_circ_300394,RMVar_hsa_circ_97438,RMVar_hsa_circ_269953,RMVar_hsa_circ_247529,RMVar_hsa_circ_247531,RMVar_hsa_circ_247533,RMVar_hsa_circ_24970,RMVar_hsa_circ_247532,RMVar_hsa_circ_247530,RMVar_hsa_circ_247528,RMVar_hsa_circ_265602,RMVar_hsa_circ_30416,RMVar_hsa_circ_9488,RMVar_hsa_circ_58296,RMVar_hsa_circ_291841,RMVar_hsa_circ_311411,RMVar_hsa_circ_95948,RMVar_hsa_circ_25725,RMVar_hsa_circ_247539,RMVar_hsa_circ_247540,RMVar_hsa_circ_247538,RMVar_hsa_circ_247541 54134 RMVar_ID_54134 Human_SNP_ID_869637574 A-to-I Human chr7 + 128502637 128502637 128502637 TAATCTTAGTTCCGCCAGGCACGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCGAGGC TAATCTTAGTTCCGCCAGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGC A G METTL2B Ensembl:ENSG00000165055 Protein coding 3'UTR GSE38233;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;Bronchiolar epithelium,BERP35T1 cell line chr7:128502636..128502637 24183664,31158229 RNA-Seq:(High) rs1386784188 Functional Loss SNV COSMIC 33..33 33 thyroid neoplasm 2 head and neck Human_RBP_ID_8219051 Human_Splice_Rec_920432 54135 RMVar_ID_54135 Human_SNP_ID_869659471 A-to-I Human chr7 - 140912101 140912101 140912101 CTACCCAGGCTGGGGTGCAGTGGCACAGTCATAGCTCACTGCAGCCTCCAACTCCTGGGCTCAAG CTACCCAGGCTGGGGTGCAGTGGCACAGTCATGGCTCACTGCAGCCTCCAACTCCTGGGCTCAAG T C BRAF Ensembl:ENSG00000157764 Protein coding intron GSE100210 HepG2 cell line chr7:140912100..140912101 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_90659,RMVar_hsa_circ_249142,RMVar_hsa_circ_126288,RMVar_hsa_circ_249169,RMVar_hsa_circ_249171,RMVar_hsa_circ_122968 54136 RMVar_ID_54136 Human_SNP_ID_869780110 A-to-I Human chr7 - 72677251 72677251 72677251 CCCACCTACTCAGGAGGCTGAGGTGGAGGATCAGTTGAGCTCAAGAGGCCGAGGCTGCAGTGAGC CCCACCTACTCAGGAGGCTGAGGTGGAGGATCTGTTGAGCTCAAGAGGCCGAGGCTGCAGTGAGC T A TYW1B Ensembl:ENSG00000277149 Protein coding intron GSE100210 HepG2 cell line chr7:72677250..72677251 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 3 liver RMVar_hsa_circ_37315,RMVar_hsa_circ_344881,RMVar_hsa_circ_43709 54137 RMVar_ID_54137 Human_SNP_ID_869930294 A-to-I Human chr7 - 56035680 56035680 56035680 AGGAGGCGGAGGTTGCAATGAGCTGAGATAGCACCACTGCACTCCAGCCTGGGCAACAGAGTGAG AGGAGGCGGAGGTTGCAATGAGCTGAGATAGCGCCACTGCACTCCAGCCTGGGCAACAGAGTGAG T C PSPH Ensembl:ENSG00000146733 Protein coding intron GSE100210 HepG2 cell line chr7:56035679..56035680 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_26107678 54138 RMVar_ID_54138 Human_SNP_ID_869933968 A-to-I Human chr7 + 135563929 135563929 135563929 GAGGTTGCTTGAGCCCAGGAGTTTGAGGCTGTAATGAGCTGTGATTGCCTCACTGCACTCCAGCC GAGGTTGCTTGAGCCCAGGAGTTTGAGGCTGTGATGAGCTGTGATTGCCTCACTGCACTCCAGCC A G NUP205 Ensembl:ENSG00000155561 Protein coding intron GSE38233 cultured B-cells chr7:135563929..135563930 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 2 pancreas RMVar_hsa_circ_125111,RMVar_hsa_circ_248697,RMVar_hsa_circ_123120,RMVar_hsa_circ_248696 54139 RMVar_ID_54139 Human_SNP_ID_870009136 A-to-I Human chr7 + 74367528 74367528 74367528 GTTTAATTTTTATACAGATGGGTTCTCACTATATTGCCCAGGCTGGTCTCAAACTTCTGAGCTCA GTTTAATTTTTATACAGATGGGTTCTCACTATTTTGCCCAGGCTGGTCTCAAACTTCTGAGCTCA A T CLIP2 Ensembl:ENSG00000106665 Protein coding intron GSE38233 cultured B-cells chr7:74367527..74367528 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_107546,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 54140 RMVar_ID_54140 Human_SNP_ID_870012454 A-to-I Human chr7 + 146170287 146170287 146170287 ACCTCAGGTGATCTGCTTGCCTTAGCCTCTCAAAGTGCTAGGATTACAGGCATTAGTGACCGTGC ACCTCAGGTGATCTGCTTGCCTTAGCCTCTCACAGTGCTAGGATTACAGGCATTAGTGACCGTGC A C CNTNAP2 Ensembl:ENSG00000174469 Protein coding intron GSE107867 ASD brains,frontal_cortex chr7:146170287..146170288 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 54141 RMVar_ID_54141 Human_SNP_ID_870060736 A-to-I Human chr7 + 128503181 128503181 128503181 AGTCCCCTGTAGTCCCAGCTACTCGGGAGGCTAAGGCAGGAGAATCGTTTGAACCTGGGAGGCAG AGTCCCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGTTTGAACCTGGGAGGCAG A G METTL2B Ensembl:ENSG00000165055 Protein coding 3'UTR GSE38233 cultured B-cells chr7:128503180..128503181 24183664 RNA-Seq:(High) rs534603716 Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 1 prostate 54142 RMVar_ID_54142 Human_SNP_ID_870134473 A-to-I Human chr7 + 66153972 66153972 66153972 GATCCCAGCTACTCGGGAGGCTGAGGCGGGGGAATCGCTTGAACCGGGGAGGCAGAGGTTGCAGT GATCCCAGCTACTCGGGAGGCTGAGGCGGGGGGATCGCTTGAACCGGGGAGGCAGAGGTTGCAGT A G CRCP Ensembl:ENSG00000241258 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr7:66153972..66153973 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_26550531 54143 RMVar_ID_54143 Human_SNP_ID_870147551 A-to-I Human chr7 + 74389778 74389778 74389778 GAAATTAGCTGGGTGTAGTGGTGTGTGCCTGTAGTCCCAGCTACTCAGGAGGCTGGGGCATGAGA GAAATTAGCTGGGTGTAGTGGTGTGTGCCTGTGGTCCCAGCTACTCAGGAGGCTGGGGCATGAGA A G CLIP2 Ensembl:ENSG00000106665 Protein coding intron GSE38233 cultured B-cells chr7:74389777..74389778 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_118036,RMVar_hsa_circ_83371,RMVar_hsa_circ_245670,RMVar_hsa_circ_80587,RMVar_hsa_circ_245682,RMVar_hsa_circ_245683,RMVar_hsa_circ_245698,RMVar_hsa_circ_7588,RMVar_hsa_circ_310263,RMVar_hsa_circ_245696,RMVar_hsa_circ_122181,RMVar_hsa_circ_316225,RMVar_hsa_circ_336550,RMVar_hsa_circ_297123,RMVar_hsa_circ_245697 54144 RMVar_ID_54144 Human_SNP_ID_870187103 A-to-I Human chr7 - 65722874 65722874 65722874 AAAATTAGCCAGGCTTGATGGTGGGCACCTGTAATCCCAGCTGCTTGGGAGGCTGAGGCAGGAGA AAAATTAGCCAGGCTTGATGGTGGGCACCTGTCATCCCAGCTGCTTGGGAGGCTGAGGCAGGAGA T G AC073107.1 Ensembl:ENSG00000272693 Pseudogene intron GSE47997 K562 cells&HepG2 cells chr7:65722873..65722874 23474544 RNA-Seq:(High) rs376620576 Functional Loss SNV ICGC 33..33 33 LICA 1 - 54145 RMVar_ID_54145 Human_SNP_ID_870190099 A-to-I Human chr7 - 140470719 140470719 140470719 CAGAGACAGGGTTTCATCATGTTGGCCAGGCTAGTCTCGAACTCCTGACCTCAAGTGATCTGCCC CAGAGACAGGGTTTCATCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAAGTGATCTGCCC T C MKRN1 Ensembl:ENSG00000133606 Protein coding intron GSE38233 cultured B-cells chr7:140470718..140470719 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_51329,RMVar_hsa_circ_249089,RMVar_hsa_circ_331662 54146 RMVar_ID_54146 Human_SNP_ID_870206268 A-to-I Human chr7 + 131426920 131426920 131426920 GGGATTACAGATGTGTGCCACCATGCCAGGCTAATTTTTGTATTTTTGGTAGAGACGGGATTTCA GGGATTACAGATGTGTGCCACCATGCCAGGCTTATTTTTGTATTTTTGGTAGAGACGGGATTTCA A T MKLN1 Ensembl:ENSG00000128585 Protein coding intron GSE100210 HepG2 cell line chr7:131426920..131426921 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_596,RMVar_hsa_circ_114367,RMVar_hsa_circ_248512,RMVar_hsa_circ_319018,RMVar_hsa_circ_126807,RMVar_hsa_circ_368252,RMVar_hsa_circ_248514,RMVar_hsa_circ_347651,RMVar_hsa_circ_365577,RMVar_hsa_circ_298980,RMVar_hsa_circ_303813,RMVar_hsa_circ_13998,RMVar_hsa_circ_62622,RMVar_hsa_circ_248525,RMVar_hsa_circ_248526,RMVar_hsa_circ_285702,RMVar_hsa_circ_343168,RMVar_hsa_circ_295320,RMVar_hsa_circ_110742,RMVar_hsa_circ_71912,RMVar_hsa_circ_17649,RMVar_hsa_circ_248527,RMVar_hsa_circ_51462,RMVar_hsa_circ_248529,RMVar_hsa_circ_248530,RMVar_hsa_circ_248528,RMVar_hsa_circ_12446,RMVar_hsa_circ_120803,RMVar_hsa_circ_33321,RMVar_hsa_circ_60460,RMVar_hsa_circ_248541,RMVar_hsa_circ_268832,RMVar_hsa_circ_34192,RMVar_hsa_circ_280059,RMVar_hsa_circ_322679,RMVar_hsa_circ_353415,RMVar_hsa_circ_37773,RMVar_hsa_circ_248542,RMVar_hsa_circ_27891,RMVar_hsa_circ_277531,RMVar_hsa_circ_349320,RMVar_hsa_circ_370623,RMVar_hsa_circ_64955,RMVar_hsa_circ_248543 54147 RMVar_ID_54147 Human_SNP_ID_870239821 A-to-I Human chr7 + 29427304 29427304 29427304 TGCCACTGCACTGCTAGCCTGGGTGATAGAGTAAGACTGTCTCAAAATAAATAAATAATAAAGGA TGCCACTGCACTGCTAGCCTGGGTGATAGAGTTAGACTGTCTCAAAATAAATAAATAATAAAGGA A T AC004593.2,CHN2 Ensembl:ENSG00000285162,Ensembl:ENSG00000106069 Protein coding,Protein coding intron,intron GSE107867 ASD brains,cerebellum chr7:29427303..29427304 30559470 RNA-Seq:(High) rs932843045 Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 4 ovary RMVar_hsa_circ_377035 54148 RMVar_ID_54148 Human_SNP_ID_870331875 A-to-I Human chr7 - 149017515 149017515 149017515 CGATGGCGCAATCTCAGCTCACCGCAACCTCCACCTCCCGGATTCAAGTGATTCTCCTGCCTCAG CGATGGCGCAATCTCAGCTCACCGCAACCTCCGCCTCCCGGATTCAAGTGATTCTCCTGCCTCAG T C PDIA4 Ensembl:ENSG00000155660 Protein coding intron GSE38233 cultured B-cells chr7:149017514..149017515 24183664 RNA-Seq:(High) rs1962977 Functional Loss SNV ICGC 33..33 33 LAML 1 - RMVar_hsa_circ_541,RMVar_hsa_circ_371845,RMVar_hsa_circ_102100,RMVar_hsa_circ_360788,RMVar_hsa_circ_249333,RMVar_hsa_circ_249335,RMVar_hsa_circ_356601,RMVar_hsa_circ_358987 54149 RMVar_ID_54149 Human_SNP_ID_870357391 A-to-I Human chr7 - 111209208 111209208 111209208 TATTTTTATTAGAGAGGGAGTTTCACTGTGTTAGCCAGAATGATCTTGATCTGCTGACCTCGTGA TATTTTTATTAGAGAGGGAGTTTCACTGTGTTTGCCAGAATGATCTTGATCTGCTGACCTCGTGA T A IMMP2L Ensembl:ENSG00000184903 Protein coding intron GSE100210 HepG2 cell line chr7:111209207..111209208 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_3042180 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 54150 RMVar_ID_54150 Human_SNP_ID_870380996 A-to-I Human chr7 + 23304725 23304725 23304725 ACTCCACAGTGCCCAGCTAATTTATTTTTTATAGAGACAGGGTCTCACTATATTGCCCAGACTCT ACTCCACAGTGCCCAGCTAATTTATTTTTTATTGAGACAGGGTCTCACTATATTGCCCAGACTCT A T MALSU1 Ensembl:ENSG00000156928 Protein coding intron GSE100210 HepG2 cell line chr7:23304724..23304725 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 RECA 1 - Human_RBP_ID_7724206,Human_RBP_ID_16113483 54151 RMVar_ID_54151 Human_SNP_ID_870449967 A-to-I Human chr7 + 42795579 42795579 42795579 GCACTCAACTGTGTGGTGGGATCCCAGGGCATACCCAAGAGAATTGTAAATGCAAAAATTGCTTG GCACTCAACTGTGTGGTGGGATCCCAGGGCATGCCCAAGAGAATTGTAAATGCAAAAATTGCTTG A G TCP1P1 Ensembl:ENSG00000229161 Pseudogene exon GSE100210 HepG2 cell line chr7:42795578..42795579 29129909 RNA-Seq:(High) rs373694560 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_7779111 54152 RMVar_ID_54152 Human_SNP_ID_870479319 A-to-I Human chr7 + 151071687 151071687 151071687 CCACCAGCTCCTGAGCTGGTTCCTACACCCCTAGGAGAGAAGACGCAGGACCTGATAGGGGTGTC CCACCAGCTCCTGAGCTGGTTCCTACACCCCTGGGAGAGAAGACGCAGGACCTGATAGGGGTGTC A G SLC4A2 Ensembl:ENSG00000164889 Protein coding intron GSE100210 HepG2 cell line chr7:151071686..151071687 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA 33..33 33 OV 1 - Human_RBP_ID_952919,Human_RBP_ID_5622669,Human_RBP_ID_22686109 RMVar_hsa_circ_95546 54153 RMVar_ID_54153 Human_SNP_ID_870563895 A-to-I Human chr7 - 55834775 55834775 55834775 AGCCGGGCGTGGTGGCGGGTGCCTGTGGTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAGTGGCG AGCCGGGCGTGGTGGCGGGTGCCTGTGGTCCCTGCTACTCGGGAGGCTGAGGCAGGAGAGTGGCG T A SEPTIN14 Ensembl:ENSG00000154997 Protein coding intron GSE100210 HepG2 cell line chr7:55834774..55834775 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_177326 RMVar_hsa_circ_23650 54154 RMVar_ID_54154 Human_SNP_ID_870569879 A-to-I Human chr7 + 101833408 101833408 101833408 GTCTCTACAGAAAAAAAAAAAAGAAAGAAATTAGCTGAGCGTGATGGTGCACACCTGTGATCCTG GTCTCTACAGAAAAAAAAAAAAGAAAGAAATTGGCTGAGCGTGATGGTGCACACCTGTGATCCTG A G CUX1 Ensembl:ENSG00000257923 Protein coding intron GSE100210 HepG2 cell line chr7:101833407..101833408 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 43 pancreas Human_RBP_ID_15947725 54155 RMVar_ID_54155 Human_SNP_ID_870583925 A-to-I Human chr7 - 110861378 110861378 110861378 CCTGTAGTCCCTCCTACTCGGGAGGATTACCTAAGCCTGGGGAGTTTGAGGATGCAGTGAGCCAA CCTGTAGTCCCTCCTACTCGGGAGGATTACCTCAGCCTGGGGAGTTTGAGGATGCAGTGAGCCAA T G IMMP2L Ensembl:ENSG00000184903 Protein coding intron GSE47997 K562 cells&HepG2 cells chr7:110861377..110861378 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - RMVar_hsa_circ_95445,RMVar_hsa_circ_109595,RMVar_hsa_circ_247831,RMVar_hsa_circ_247832 54156 RMVar_ID_54156 Human_SNP_ID_870606426 A-to-I Human chr7 - 73461839 73461839 73461839 GAGATCCTCCTACCTCAGCCTCTCAAAATGCTAGGATTATAGGCATGAGCCACCTCACCCAGCCA GAGATCCTCCTACCTCAGCCTCTCAAAATGCTGGGATTATAGGCATGAGCCACCTCACCCAGCCA T C BAZ1B Ensembl:ENSG00000009954 Protein coding intron GSE47997;GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line chr7:73461838..73461839 23474544,29129909,31158229 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_59672,RMVar_hsa_circ_1418,RMVar_hsa_circ_87909,RMVar_hsa_circ_98461,RMVar_hsa_circ_306295,RMVar_hsa_circ_74266,RMVar_hsa_circ_245552,RMVar_hsa_circ_245553,RMVar_hsa_circ_99589,RMVar_hsa_circ_319221,RMVar_hsa_circ_74779,RMVar_hsa_circ_245554,RMVar_hsa_circ_245555,RMVar_hsa_circ_325430,RMVar_hsa_circ_318930,RMVar_hsa_circ_15416,RMVar_hsa_circ_372776,RMVar_hsa_circ_49126,RMVar_hsa_circ_245558,RMVar_hsa_circ_293924,RMVar_hsa_circ_371252,RMVar_hsa_circ_378325,RMVar_hsa_circ_307773,RMVar_hsa_circ_292795,RMVar_hsa_circ_70156,RMVar_hsa_circ_273435,RMVar_hsa_circ_69359,RMVar_hsa_circ_245561,RMVar_hsa_circ_245563,RMVar_hsa_circ_245564,RMVar_hsa_circ_245562,RMVar_hsa_circ_245560 54157 RMVar_ID_54157 Human_SNP_ID_870608749 A-to-I Human chr7 - 23564163 23564163 23564163 ACAGGAATGCAAAAAGAGTTGTCCTGTAGTTCAAATGGGAGAATTATGCATAGAAGTTACACCCC ACAGGAATGCAAAAAGAGTTGTCCTGTAGTTCGAATGGGAGAATTATGCATAGAAGTTACACCCC T C AC006026.1 Ensembl:ENSG00000224785 Pseudogene exon GSE100210 HepG2 cell line chr7:23564162..23564163 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 1 - 54158 RMVar_ID_54158 Human_SNP_ID_870638553 A-to-I Human chr7 - 44078382 44078382 44078382 AGCTCACGGCAGCCTTGACTTCCTGGGCTCAAACCATCCTCCCACCTCAGTCTCTGGAGTAGCTG AGCTCACGGCAGCCTTGACTTCCTGGGCTCAATCCATCCTCCCACCTCAGTCTCTGGAGTAGCTG T A POLM Ensembl:ENSG00000122678 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr7:44078381..44078382 24183664,29129909 RNA-Seq:(High) rs982324517 Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_Splice_Rec_861515 RMVar_hsa_circ_244909,RMVar_hsa_circ_100387,RMVar_hsa_circ_34282 54159 RMVar_ID_54159 Human_SNP_ID_870646169 A-to-I Human chr7 + 38230183 38230183 38230183 CTGAGCCTGATGTGTTAACAAATAGGTGAAGAAAGTCTTGTGCTGTATTCCTAATCAAAAGACTT CTGAGCCTGATGTGTTAACAAATAGGTGAAGACAGTCTTGTGCTGTATTCCTAATCAAAAGACTT A C STARD3NL Ensembl:ENSG00000010270 Protein coding 3'UTR GSE100210 HepG2 cell line chr7:38230183..38230184 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_683856,Human_RBP_ID_1051951,Human_RBP_ID_1221360,Human_RBP_ID_2042302,Human_RBP_ID_16148901,Human_RBP_ID_18099867,Human_RBP_ID_18382093,Human_RBP_ID_21904459,Human_RBP_ID_24214227,Human_RBP_ID_27768154 RMVar_hsa_circ_96400,RMVar_hsa_circ_244699 54160 RMVar_ID_54160 Human_SNP_ID_870666990 A-to-I Human chr7 - 129889763 129889763 129889763 CCCAGGCTGGTCTCGGACTCCTGGCCTCAAGCAATCTTTCTGCCCTTGCTTCCCAAAGTGTTGGG CCCAGGCTGGTCTCGGACTCCTGGCCTCAAGCTATCTTTCTGCCCTTGCTTCCCAAAGTGTTGGG T A UBE2H Ensembl:ENSG00000186591 Protein coding intron GSE100210 HepG2 cell line chr7:129889762..129889763 29129909 RNA-Seq:(High) rs1563035601 Functional Loss SNV ICGC 33..33 33 MALY 1 - 54161 RMVar_ID_54161 Human_SNP_ID_870684385 A-to-I Human chr7 + 80377417 80377417 80377417 TGTGATGCCTTCAGCTTTTTTTTTTTTTTAATATTCTCTTAAGAGTTTATTATAAACCAGTTTCA TGTGATGCCTTCAGCTTTTTTTTTTTTTTAATTTTCTCTTAAGAGTTTATTATAAACCAGTTTCA A T CD36 Ensembl:ENSG00000135218 Protein coding intron GSE100210 HepG2 cell line chr7:80377416..80377417 29129909 RNA-Seq:(High) rs1312794689 Functional Loss SNV ICGC 33..33 33 PRAD 1 - 54162 RMVar_ID_54162 Human_SNP_ID_870723405 A-to-I Human chr7 + 105041540 105041540 105041540 TCTCCTGCCTCAGCCTCCCGAGTAGCTGTATTACAGGCGTGTGTCACCACGCCCAGCTAATTTTT TCTCCTGCCTCAGCCTCCCGAGTAGCTGTATTGCAGGCGTGTGTCACCACGCCCAGCTAATTTTT A G KMT2E Ensembl:ENSG00000005483 Protein coding intron GSE100210 HepG2 cell line chr7:105041539..105041540 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 4 liver RMVar_hsa_circ_6704,RMVar_hsa_circ_118314,RMVar_hsa_circ_278570,RMVar_hsa_circ_370704,RMVar_hsa_circ_320297,RMVar_hsa_circ_312768,RMVar_hsa_circ_264827,RMVar_hsa_circ_118535,RMVar_hsa_circ_85463,RMVar_hsa_circ_62855,RMVar_hsa_circ_247513,RMVar_hsa_circ_247517,RMVar_hsa_circ_247519,RMVar_hsa_circ_247521,RMVar_hsa_circ_247520,RMVar_hsa_circ_247518,RMVar_hsa_circ_247515,RMVar_hsa_circ_247516,RMVar_hsa_circ_247514,RMVar_hsa_circ_247525,RMVar_hsa_circ_268874,RMVar_hsa_circ_297368,RMVar_hsa_circ_328971,RMVar_hsa_circ_343320,RMVar_hsa_circ_315721,RMVar_hsa_circ_60526,RMVar_hsa_circ_75002,RMVar_hsa_circ_247526,RMVar_hsa_circ_247527 54163 RMVar_ID_54163 Human_SNP_ID_870769112 A-to-I Human chr7 + 134955294 134955294 134955294 CATCTGTAGTCCCAGCTACTCGACGCTGAGGCAGAAGAATCACTTGAACCCGGGAGGTGGAGATT CATCTGTAGTCCCAGCTACTCGACGCTGAGGCGGAAGAATCACTTGAACCCGGGAGGTGGAGATT A G CALD1 Ensembl:ENSG00000122786 Protein coding intron GSE100210 HepG2 cell line chr7:134955293..134955294 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 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 54164 RMVar_ID_54164 Human_SNP_ID_870770402 A-to-I Human chr7 - 66990157 66990157 66990157 AAAATAGTCTGGCGTGGTGGCACATGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAA AAAATAGTCTGGCGTGGTGGCACATGCCTGTACTCCCAGCTACTCGGGAGGCTGAGGCAGGAGAA T G SBDS Ensembl:ENSG00000126524 Protein coding intron GSE100210 HepG2 cell line chr7:66990156..66990157 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_96068,RMVar_hsa_circ_245407 54165 RMVar_ID_54165 Human_SNP_ID_870886272 A-to-I Human chr7 - 65975025 65975025 65975025 ACAGACGTCACTGGGGCCTGTGTCTGACTTCTACACACTCCCTGTGGGGATCCGCACTGTGGCTG ACAGACGTCACTGGGGCCTGTGTCTGACTTCTGCACACTCCCTGTGGGGATCCGCACTGTGGCTG T C GUSB Ensembl:ENSG00000169919 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector chr7:65975024..65975025 29967493 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC 33..33 33 BRCA 2 - Human_Splice_Rec_870518,Human_Splice_Rec_870544,Human_Splice_Rec_870562,Human_Splice_Rec_870580,Human_Splice_Rec_870628 Human_miRNA_ID_658816,Human_miRNA_ID_1960385,Human_miRNA_ID_1983344,Human_miRNA_ID_2910041 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_329280,RMVar_hsa_circ_119821,RMVar_hsa_circ_280932,RMVar_hsa_circ_245310,RMVar_hsa_circ_245309,RMVar_hsa_circ_245307,RMVar_hsa_circ_245311 54166 RMVar_ID_54166 Human_SNP_ID_870927163 A-to-I Human chr7 - 139073133 139073133 139073133 CACCACCACACCCAGCTAATTTTTGTATTTTTAGTAGACATGGGGTTTCAACATGTTGGACAGGC CACCACCACACCCAGCTAATTTTTGTATTTTTGGTAGACATGGGGTTTCAACATGTTGGACAGGC T C ZC3HAV1 Ensembl:ENSG00000105939 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr7:139073132..139073133 24183664,29129909 RNA-Seq:(High) rs1388782548 Functional Loss SNV ICGC 33..33 33 MELA 1 - 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 54167 RMVar_ID_54167 Human_SNP_ID_870927547 A-to-I Human chr7 + 77011184 77011184 77011184 AAAATTAGCCAGGCATGGTGATGGGCGCCTGTAATTTCAGCTACTTGGGAGGCTGAGGCAGGAGA AAAATTAGCCAGGCATGGTGATGGGCGCCTGTCATTTCAGCTACTTGGGAGGCTGAGGCAGGAGA A C DTX2P1-UPK3BP1-PMS2P11 Ensembl:ENSG00000265479 lincRNA intron GSE100210 HepG2 cell line chr7:77011184..77011185 29129909 RNA-Seq:(High) rs183987296 Functional Loss SNV ICGC 33..33 33 COCA 1 - RMVar_hsa_circ_16068,RMVar_hsa_circ_265160 54168 RMVar_ID_54168 Human_SNP_ID_870934118 A-to-I Human chr7 - 16089209 16089209 16089209 ATATACGTACGCATACACACATATATGTATATACGTACGTATATACACACATATATGTATATACG ATATACGTACGCATACACACATATATGTATATGCGTACGTATATACACACATATATGTATATACG T C CRPPA Ensembl:ENSG00000214960 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells chr7:16089208..16089209 23474544 RNA-Seq:(High) rs995512667 Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_112717,RMVar_hsa_circ_116458,RMVar_hsa_circ_243875,RMVar_hsa_circ_243876 54169 RMVar_ID_54169 Human_SNP_ID_870949107 A-to-I Human chr7 - 23564141 23564141 23564141 CCTGTAGTTCAAATGGGAGAATTATGCATAGAAGTTACACCCCAGAGCAAAATAGCATGGATTTC CCTGTAGTTCAAATGGGAGAATTATGCATAGAGGTTACACCCCAGAGCAAAATAGCATGGATTTC T C AC006026.1 Ensembl:ENSG00000224785 Pseudogene exon GSE100210 HepG2 cell line chr7:23564140..23564141 29129909 RNA-Seq:(High) rs1049267824 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_4935741 54170 RMVar_ID_54170 Human_SNP_ID_870949111 A-to-I Human chr7 - 23564141 23564141 23564141 CCTGTAGTTCAAATGGGAGAATTATGCATAGAAGTTACACCCCAGAGCAAAATAGCATGGATTTC CCTGTAGTTCAAATGGGAGAATTATGCATAGACGTTACACCCCAGAGCAAAATAGCATGGATTTC T G AC006026.1 Ensembl:ENSG00000224785 Pseudogene exon GSE100210 HepG2 cell line chr7:23564140..23564141 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_4935741 54171 RMVar_ID_54171 Human_SNP_ID_870995290 A-to-I Human chr7 - 117847483 117847483 117847483 TTGCCCAGGCTGGAGTGCAGTGGCATGATCTTAGCTCACTGCAACATCTGCCTCCTGATTTAAGC TTGCCCAGGCTGGAGTGCAGTGGCATGATCTTCGCTCACTGCAACATCTGCCTCCTGATTTAAGC T G CTTNBP2 Ensembl:ENSG00000077063 Protein coding intron GSE100210 HepG2 cell line chr7:117847482..117847483 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 UTCA,endometrium carcinosarcoma-malignant_mesodermal_mixed_tumour 2 uterus RMVar_hsa_circ_86232,RMVar_hsa_circ_247973,RMVar_hsa_circ_378361 54172 RMVar_ID_54172 Human_SNP_ID_871014453 A-to-I Human chr7 + 4755557 4755557 4755557 AGGAGGAGGATCAAGACCAGCCTGTGCAACATAGAGAGAACCTCTTTTCTACTAAAAATTAGCTG AGGAGGAGGATCAAGACCAGCCTGTGCAACATGGAGAGAACCTCTTTTCTACTAAAAATTAGCTG A G FOXK1 Ensembl:ENSG00000164916 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr7:4755556..4755557 24183664,29129909 RNA-Seq:(High) rs1398333153 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue RMVar_hsa_circ_365207,RMVar_hsa_circ_333414,RMVar_hsa_circ_46595,RMVar_hsa_circ_243448 54173 RMVar_ID_54173 Human_SNP_ID_871081582 A-to-I Human chr7 + 98918792 98918792 98918792 AAAGTTCATATGTTGGCCAGGCACTGTGGCTCACGCCTGTAATCCCAGCACTATGGGAGGCTGAG AAAGTTCATATGTTGGCCAGGCACTGTGGCTCGCGCCTGTAATCCCAGCACTATGGGAGGCTGAG A G TRRAP Ensembl:ENSG00000196367 Protein coding intron GSE38233 cultured B-cells chr7:98918791..98918792 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 5 pancreas RMVar_hsa_circ_66503,RMVar_hsa_circ_125590,RMVar_hsa_circ_80773,RMVar_hsa_circ_246796,RMVar_hsa_circ_10888,RMVar_hsa_circ_246800,RMVar_hsa_circ_95390,RMVar_hsa_circ_98787,RMVar_hsa_circ_246805,RMVar_hsa_circ_246806,RMVar_hsa_circ_112413,RMVar_hsa_circ_246808,RMVar_hsa_circ_97292,RMVar_hsa_circ_126943,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_246818,RMVar_hsa_circ_246823,RMVar_hsa_circ_109026,RMVar_hsa_circ_106098,RMVar_hsa_circ_246825,RMVar_hsa_circ_246826,RMVar_hsa_circ_372956,RMVar_hsa_circ_71857,RMVar_hsa_circ_246827,RMVar_hsa_circ_83393,RMVar_hsa_circ_126463,RMVar_hsa_circ_246828,RMVar_hsa_circ_125823,RMVar_hsa_circ_116768,RMVar_hsa_circ_40081,RMVar_hsa_circ_119702,RMVar_hsa_circ_246830,RMVar_hsa_circ_246831,RMVar_hsa_circ_246832,RMVar_hsa_circ_246834,RMVar_hsa_circ_80776,RMVar_hsa_circ_246835 54174 RMVar_ID_54174 Human_SNP_ID_871137179 A-to-I Human chr7 + 102454271 102454271 102454271 CAAAAATTACCCGGGCTTGGTGGCTCGTGCCTATAGTCCCAGCTACTGGGGAGGCTGAGGTGGGA CAAAAATTACCCGGGCTTGGTGGCTCGTGCCTGTAGTCCCAGCTACTGGGGAGGCTGAGGTGGGA A G ORAI2 Ensembl:ENSG00000160991 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr7:102454270..102454271 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 3 prostate 54175 RMVar_ID_54175 Human_SNP_ID_871354520 A-to-I Human chr7 + 102441010 102441010 102441010 TGCCTCCTGGATTCAAGCGATTCTCCTGCCTCAGCCTTTCGAGTAGCTGGGACTACAGGCACACA TGCCTCCTGGATTCAAGCGATTCTCCTGCCTCGGCCTTTCGAGTAGCTGGGACTACAGGCACACA A G ORAI2 Ensembl:ENSG00000160991 Protein coding intron GSE38233 cultured B-cells chr7:102441009..102441010 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 54176 RMVar_ID_54176 Human_SNP_ID_871394688 A-to-I Human chr7 - 38723460 38723460 38723460 TCGGCCTTCCGAAGTGTTAGGATTACAGGCGTAAGTCACCATGCCCAGCCAAGAAAGCTATTCTT TCGGCCTTCCGAAGTGTTAGGATTACAGGCGTGAGTCACCATGCCCAGCCAAGAAAGCTATTCTT T C VPS41 Ensembl:ENSG00000006715 Protein coding 3'UTR GSE38233 cultured B-cells chr7:38723459..38723460 24183664 RNA-Seq:(High) rs3207255 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 2 large intestine 54177 RMVar_ID_54177 Human_SNP_ID_871402454 A-to-I Human chr7 - 103141451 103141451 103141451 AAGCTCCTGGCTGATCAGGCTGAGGCCCGCAGATCTAAGACCAAGGAAGCACACAAGAGCTATGA AAGCTCCTGGCTGATCAGGCTGAGGCCCGCAGGTCTAAGACCAAGGAAGCACACAAGAGCTATGA T C AC007683.1,NAPEPLD Ensembl:ENSG00000224415,Ensembl:ENSG00000161048 Pseudogene,Protein coding exon,intron GSE107867 ASD brains,frontal_cortex chr7:103141450..103141451 30559470 RNA-Seq:(High) rs1403133751 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 5 haematopoietic and lymphoid tissue 54178 RMVar_ID_54178 Human_SNP_ID_871449095 A-to-I Human chr7 + 77779461 77779461 77779461 AGAGCTGACATTAACATATATATATATATATAAATATATATATATATTTTGTAATATGAGCCAGA AGAGCTGACATTAACATATATATATATATATATATATATATATATATTTTGTAATATGAGCCAGA A T RSBN1L Ensembl:ENSG00000187257 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells chr7:77779461..77779462 23474544 RNA-Seq:(High) rs4729744 Functional Loss SNV TCGA,ICGC 33..33 33 BRCA,LUSC 3 - Human_miRNA_ID_155175 RMVar_hsa_circ_245955,RMVar_hsa_circ_265948,RMVar_hsa_circ_268970,RMVar_hsa_circ_266006 54179 RMVar_ID_54179 Human_SNP_ID_871455936 A-to-I Human chr7 - 44575833 44575833 44575833 GAGATCGAGACCATCCTGGCTAACAACGGTGAAACCCTGTCTCTACTAAAAATACAAAAAATTAG GAGATCGAGACCATCCTGGCTAACAACGGTGAGACCCTGTCTCTACTAAAAATACAAAAAATTAG T C - - Other Unknown GSE100210 HepG2 cell line chr7:44575832..44575833 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 54180 RMVar_ID_54180 Human_SNP_ID_871489355 A-to-I Human chr7 - 140466023 140466023 140466023 AGGCTGGAGTGCAGTGGCGTGATCTCGGCTCAATGCAATGTCCGCCTCCTGGGTTCAAGCGATTC AGGCTGGAGTGCAGTGGCGTGATCTCGGCTCAGTGCAATGTCCGCCTCCTGGGTTCAAGCGATTC T C MKRN1 Ensembl:ENSG00000133606 Protein coding intron GSE38233 cultured B-cells chr7:140466022..140466023 24183664 RNA-Seq:(High) rs148889998 Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_51329,RMVar_hsa_circ_249089,RMVar_hsa_circ_331662 54181 RMVar_ID_54181 Human_SNP_ID_871678183 A-to-I Human chr7 - 75410779 75410779 75410779 CCAGTCCCGCCGTGCACGGCAGCGGGGCTGAAACCAGATGACAAAGCGCTGACCGTCGGGGTTCA CCAGTCCCGCCGTGCACGGCAGCGGGGCTGAACCCAGATGACAAAGCGCTGACCGTCGGGGTTCA T G - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr7:75410778..75410779 30559470 RNA-Seq:(High) rs797026271 Functional Loss SNV ICGC 33..33 33 PBCA 1 - 54182 RMVar_ID_54182 Human_SNP_ID_871786431 A-to-I Human chr7 - 55458310 55458302 55458311 CTTCAAAACATTACAGGGCTATGGTAACCCAAAGAGCATAGTATTGATATAAACAGACACACAGA CTTCAAAACATTACAGGGCTATGGTAACCCA_________GTATTGATATAAACAGACACACAGA CTATGCTCTT C VOPP1 Ensembl:ENSG00000154978 Protein coding intron GSE100210 HepG2 cell line chr7:55458309..55458310 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 32..40 33 PAAD 1 - 54183 RMVar_ID_54183 Human_SNP_ID_871800675 A-to-I Human chr7 + 74669735 74669735 74669735 TTGTATTATTAGTAGAGACGGGGTTTCACCATATTGGCCAGGCTGGTCTCAAATTCCTGACTTTG TTGTATTATTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGGTCTCAAATTCCTGACTTTG A G GTF2I Ensembl:ENSG00000263001 Protein coding intron GSE38233 cultured B-cells chr7:74669734..74669735 24183664 RNA-Seq:(High) rs1299210480 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 haematopoietic and lymphoid tissue 54184 RMVar_ID_54184 Human_SNP_ID_871812162 A-to-I Human chr7 + 120581837 120581837 120581837 GCGTTCATGCAATTCTCCTGCCTCAGCAGCCCAAGTAGCTGGGATTACAGACATGCACCACCAAA GCGTTCATGCAATTCTCCTGCCTCAGCAGCCCCAGTAGCTGGGATTACAGACATGCACCACCAAA A C KCND2 Ensembl:ENSG00000184408 Protein coding intron GSE107867 ASD brains,cerebellum chr7:120581836..120581837 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 2 oesophagus 54185 RMVar_ID_54185 Human_SNP_ID_871822048 A-to-I Human chr7 - 44033830 44033830 44033830 CAGACTGGAGTGCAATGGCACGATCTCAGCTCACTGCAATCTCCACCTCCCAGGGTCAAGCAATT CAGACTGGAGTGCAATGGCACGATCTCAGCTCGCTGCAATCTCCACCTCCCAGGGTCAAGCAATT T C AC017116.2,RASA4CP Ensembl:ENSG00000285596,Ensembl:ENSG00000228903 lincRNA,Pseudogene intron,intron GSE47997 K562 cells&HepG2 cells chr7:44033829..44033830 23474544 RNA-Seq:(High) rs778252058 Functional Loss SNV ICGC 33..33 33 LUSC 1 - 54186 RMVar_ID_54186 Human_SNP_ID_871825719 A-to-I Human chr7 - 66543755 66543755 66543755 CTGGGAGGTGGAGGTTGCAGTGAGCAGAGATCATGTCACTGCACTGCAGCCTGGGAGACAGAGAC CTGGGAGGTGGAGGTTGCAGTGAGCAGAGATCGTGTCACTGCACTGCAGCCTGGGAGACAGAGAC T C AC006001.3 Ensembl:ENSG00000229180 Pseudogene intron GSE100210 HepG2 cell line chr7:66543754..66543755 29129909 RNA-Seq:(High) rs1157759938 Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_17427680,Human_RBP_ID_26138608 RMVar_hsa_circ_90413,RMVar_hsa_circ_86385,RMVar_hsa_circ_245353,RMVar_hsa_circ_245354,RMVar_hsa_circ_317819,RMVar_hsa_circ_245357 54187 RMVar_ID_54187 Human_SNP_ID_871846967 A-to-I Human chr7 - 98239549 98239548 98239550 GGATTTCTTTTTTTTATTTTTTAATTTGAGACAGAGTCTCGTTCCGTCACCCAGGCTGGAATGCC GGATTTCTTTTTTTTATTTTTTAATTTGAGA__GAGTCTCGTTCCGTCACCCAGGCTGGAATGCC CTG C TECPR1 Ensembl:ENSG00000205356 Protein coding intron GSE100210 HepG2 cell line chr7:98239548..98239549 29129909 RNA-Seq:(High) rs530487687 Functional Loss DEL ICGC 32..33 33 PBCA 1 - RMVar_hsa_circ_60094,RMVar_hsa_circ_515,RMVar_hsa_circ_370245,RMVar_hsa_circ_246773,RMVar_hsa_circ_73829,RMVar_hsa_circ_246776 54188 RMVar_ID_54188 Human_SNP_ID_871881894 A-to-I Human chr7 - 17926664 17926664 17926664 TAGGCTGATCTCAAACTCCCGAGCTCAAAGTAATCCATCCACCTCAGCCTCCCAAAGTGATGGAT TAGGCTGATCTCAAACTCCCGAGCTCAAAGTATTCCATCCACCTCAGCCTCCCAAAGTGATGGAT T A SNX13 Ensembl:ENSG00000071189 Protein coding intron GSE100210 HepG2 cell line chr7:17926663..17926664 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 54189 RMVar_ID_54189 Human_SNP_ID_871935557 A-to-I Human chr7 - 158641465 158641465 158641465 AATCTATCCTTCTGCCTCAGTCCCAATTGGCTAGGACTGCAGGCACACACCACCAGACCCAGCTA AATCTATCCTTCTGCCTCAGTCCCAATTGGCTGGGACTGCAGGCACACACCACCAGACCCAGCTA T C NCAPG2 Ensembl:ENSG00000146918 Protein coding intron GSE100210 HepG2 cell line chr7:158641464..158641465 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_7719485,Human_RBP_ID_16101787,Human_RBP_ID_21471365 Human_Splice_Rec_943628 54190 RMVar_ID_54190 Human_SNP_ID_872020914 A-to-I Human chr7 + 74227920 74227920 74227920 AGAAGAGGCCAGGCGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGCTG AGAAGAGGCCAGGCGCAGTGGCTCACGCCTGTGATCCCAGCACTTTGGGAGGCTGAGGCAGGCTG A G LAT2 Ensembl:ENSG00000086730 Protein coding intron GSE38233 cultured B-cells chr7:74227919..74227920 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 CMDI 1 - 54191 RMVar_ID_54191 Human_SNP_ID_872035000 A-to-I Human chr7 + 146388175 146388175 146388175 GCTTTTGGCCGGGCATGAGGTCTCACGTTGGTAATCCTCGCACTTTGAGACGCTGAGGCAGGAGG GCTTTTGGCCGGGCATGAGGTCTCACGTTGGTTATCCTCGCACTTTGAGACGCTGAGGCAGGAGG A T CNTNAP2 Ensembl:ENSG00000174469 Protein coding intron GSE107867 ASD brains,frontal_cortex chr7:146388175..146388176 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 2 pancreas 54192 RMVar_ID_54192 Human_SNP_ID_872036656 A-to-I Human chr7 + 74110648 74110648 74110648 CTCCACCTCCCAGGTTCAATCGATTCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGAGCCCA CTCCACCTCCCAGGTTCAATCGATTCTGCCTCTGCCTCCCGAGTAGCTGGGATTACAGGAGCCCA A T LIMK1 Ensembl:ENSG00000106683 Protein coding intron GSE38233 cultured B-cells chr7:74110647..74110648 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 UTCA 1 - RMVar_hsa_circ_25378,RMVar_hsa_circ_124213,RMVar_hsa_circ_245615,RMVar_hsa_circ_369982,RMVar_hsa_circ_102293,RMVar_hsa_circ_98103,RMVar_hsa_circ_245618,RMVar_hsa_circ_245619,RMVar_hsa_circ_84925,RMVar_hsa_circ_245622,RMVar_hsa_circ_313114,RMVar_hsa_circ_105840,RMVar_hsa_circ_245624,RMVar_hsa_circ_365489,RMVar_hsa_circ_245626 54193 RMVar_ID_54193 Human_SNP_ID_872073911 A-to-I Human chr7 - 16617709 16617709 16617709 CTCCTGCCTCAGCCTCCCAAAGTGCTGGGATTATAGGCATGAGCCACCATGCCTGCCCTTCATCC CTCCTGCCTCAGCCTCCCAAAGTGCTGGGATTGTAGGCATGAGCCACCATGCCTGCCCTTCATCC T C ANKMY2 Ensembl:ENSG00000106524 Protein coding intron GSE100210 HepG2 cell line chr7:16617708..16617709 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_835,RMVar_hsa_circ_32257,RMVar_hsa_circ_243893,RMVar_hsa_circ_10078,RMVar_hsa_circ_243895,RMVar_hsa_circ_316176,RMVar_hsa_circ_243896,RMVar_hsa_circ_316295,RMVar_hsa_circ_52426,RMVar_hsa_circ_348817,RMVar_hsa_circ_243897,RMVar_hsa_circ_331810 54194 RMVar_ID_54194 Human_SNP_ID_872091288 A-to-I Human chr7 - 73460685 73460685 73460685 GGCCAGGAGTTTGAGACCAGCCTGCGCAACATAGTGAGACCCTGTCTCTAAAAAGAATTTAAAAA GGCCAGGAGTTTGAGACCAGCCTGCGCAACATGGTGAGACCCTGTCTCTAAAAAGAATTTAAAAA T C BAZ1B Ensembl:ENSG00000009954 Protein coding intron GSE38233 cultured B-cells chr7:73460684..73460685 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_59672,RMVar_hsa_circ_1418,RMVar_hsa_circ_87909,RMVar_hsa_circ_98461,RMVar_hsa_circ_306295,RMVar_hsa_circ_74266,RMVar_hsa_circ_245552,RMVar_hsa_circ_245553,RMVar_hsa_circ_99589,RMVar_hsa_circ_319221,RMVar_hsa_circ_74779,RMVar_hsa_circ_245554,RMVar_hsa_circ_245555,RMVar_hsa_circ_325430,RMVar_hsa_circ_318930,RMVar_hsa_circ_15416,RMVar_hsa_circ_372776,RMVar_hsa_circ_49126,RMVar_hsa_circ_245558,RMVar_hsa_circ_293924,RMVar_hsa_circ_371252,RMVar_hsa_circ_378325,RMVar_hsa_circ_307773,RMVar_hsa_circ_292795,RMVar_hsa_circ_70156,RMVar_hsa_circ_273435,RMVar_hsa_circ_69359,RMVar_hsa_circ_245561,RMVar_hsa_circ_245563,RMVar_hsa_circ_245564,RMVar_hsa_circ_245562,RMVar_hsa_circ_245560 54195 RMVar_ID_54195 Human_SNP_ID_817820094 A-to-I Human chr13 - 21375072 21375072 21375072 AGGAGTGCAGTGGCGGGATCTTGGCTCGCTGCAACCTCTGCCTTCCAGGTTCAATAGAGTCTCCT AGGAGTGCAGTGGCGGGATCTTGGCTCGCTGCGACCTCTGCCTTCCAGGTTCAATAGAGTCTCCT T C ZDHHC20 Ensembl:ENSG00000180776 Protein coding 3'UTR GSE112787;GSE123020:GSM3490832,GSM3490833,GSM3490834 293 Flip-In T-REx cells,empty vector;esophageal squamous carcinoma cells,KYSE180 cell line chr13:21375071..21375072 29967493,32596459 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue Human_RBP_ID_23159657 RMVar_hsa_circ_82999,RMVar_hsa_circ_104322,RMVar_hsa_circ_112681,RMVar_hsa_circ_88460,RMVar_hsa_circ_162151,RMVar_hsa_circ_162153,RMVar_hsa_circ_162154,RMVar_hsa_circ_162152 54196 RMVar_ID_54196 Human_SNP_ID_817837260 A-to-I Human chr13 + 52630436 52630436 52630436 AGCTGGGATTACAGGTGTGCACCACCATGCCCAGCTCATTTTTGTATTTTTAGTAGAGACAGGGT AGCTGGGATTACAGGTGTGCACCACCATGCCCTGCTCATTTTTGTATTTTTAGTAGAGACAGGGT A T MRPS31P4,AL137058.2 Ensembl:ENSG00000250299,Ensembl:ENSG00000273784 Pseudogene,lincRNA intron,intron GSE38233 cultured B-cells chr13:52630435..52630436 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - RMVar_hsa_circ_16683,RMVar_hsa_circ_296738,RMVar_hsa_circ_163563,RMVar_hsa_circ_27734,RMVar_hsa_circ_122428,RMVar_hsa_circ_163564,RMVar_hsa_circ_163562,RMVar_hsa_circ_357936,RMVar_hsa_circ_345949,RMVar_hsa_circ_345086 54197 RMVar_ID_54197 Human_SNP_ID_817838391 A-to-I Human chr13 - 45400743 45400736 45400743 CCTGTAATCTTAGGACTTTGGAAGGCCGAGGCAGGAGGATCACTTGAGCCTAGGAATTCAAGACC CCTGTAATCTTAGGACTTTGGAAGGCCGAGGC_______TCACTTGAGCCTAGGAATTCAAGACC ATCCTCCT A SLC25A30 Ensembl:ENSG00000174032 Protein coding intron GSE100210 HepG2 cell line chr13:45400742..45400743 29129909 RNA-Seq:(High) rs1160880116 Functional Loss DEL ICGC 33..39 33 PBCA 1 - RMVar_hsa_circ_60502,RMVar_hsa_circ_338087,RMVar_hsa_circ_267666,RMVar_hsa_circ_267870,RMVar_hsa_circ_348619,RMVar_hsa_circ_8126,RMVar_hsa_circ_51952 54198 RMVar_ID_54198 Human_SNP_ID_817896904 A-to-I Human chr13 + 45360198 45360198 45360198 GCTGGAGTGCAATGGCAAGATCTCAGCTCACCACAACCTCTGCCTTCTTTTTTCTTCTGTTTTTA GCTGGAGTGCAATGGCAAGATCTCAGCTCACCCCAACCTCTGCCTTCTTTTTTCTTCTGTTTTTA A C TPT1-AS1 Ensembl:ENSG00000170919 lincRNA intron GSE47997 K562 cells&HepG2 cells chr13:45360197..45360198 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_Splice_Rec_1461446,Human_Splice_Rec_1461447,Human_Splice_Rec_1461706 RMVar_hsa_circ_126449,RMVar_hsa_circ_163183,RMVar_hsa_circ_122316,RMVar_hsa_circ_163185 54199 RMVar_ID_54199 Human_SNP_ID_817919876 A-to-I Human chr13 + 19673031 19673031 19673031 TGAGCCGTGAAAGGCCACTGCACTCCAGCCTGAGTGACAGAATGAGACCTTGTCTCAAAAAAAAA TGAGCCGTGAAAGGCCACTGCACTCCAGCCTGGGTGACAGAATGAGACCTTGTCTCAAAAAAAAA A G MPHOSPH8 Ensembl:ENSG00000196199 Protein coding 3'UTR GSE38233 cultured B-cells chr13:19673030..19673031 24183664 RNA-Seq:(High) rs4769866 Functional Loss SNV ICGC 33..33 33 COCA 5 - Human_RBP_ID_26424693 54200 RMVar_ID_54200 Human_SNP_ID_817991747 A-to-I Human chr13 - 49725719 49725719 49725719 GAATCACTTGAACCCCAGAGGCAGAGATTGCAATGAGTCAAGATGGCGCCACTGCACTCCCGCCT GAATCACTTGAACCCCAGAGGCAGAGATTGCAGTGAGTCAAGATGGCGCCACTGCACTCCCGCCT T C KPNA3 Ensembl:ENSG00000102753 Protein coding intron GSE100210 HepG2 cell line chr13:49725718..49725719 29129909 RNA-Seq:(High) rs964161274 Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 3 pancreas RMVar_hsa_circ_11679,RMVar_hsa_circ_163403,RMVar_hsa_circ_77144,RMVar_hsa_circ_126577,RMVar_hsa_circ_20643,RMVar_hsa_circ_276531,RMVar_hsa_circ_163410,RMVar_hsa_circ_96101,RMVar_hsa_circ_163411,RMVar_hsa_circ_163409,RMVar_hsa_circ_317931,RMVar_hsa_circ_49037,RMVar_hsa_circ_163417,RMVar_hsa_circ_163416,RMVar_hsa_circ_283035,RMVar_hsa_circ_296058,RMVar_hsa_circ_163418 54201 RMVar_ID_54201 Human_SNP_ID_818002025 A-to-I Human chr13 + 96582883 96582883 96582883 GCAGGAAGCCCAGTTAAATTTTGATTTTAGATAAACTACAAATAATTTTTTTGTATAAGTATGTT GCAGGAAGCCCAGTTAAATTTTGATTTTAGATGAACTACAAATAATTTTTTTGTATAAGTATGTT A G HS6ST3 Ensembl:ENSG00000185352 Protein coding intron GSE100210 HepG2 cell line chr13:96582882..96582883 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 54202 RMVar_ID_54202 Human_SNP_ID_818071251 A-to-I Human chr13 + 89361451 89361451 89361451 GTCACTTCTCACAAAGCATTTTGAACATTCTGAACAAACAAATTTCTTCTCACCTGTATGTGTTC GTCACTTCTCACAAAGCATTTTGAACATTCTGGACAAACAAATTTCTTCTCACCTGTATGTGTTC A G - - Other Unknown GSE100210 HepG2 cell line chr13:89361450..89361451 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 2 - 54203 RMVar_ID_54203 Human_SNP_ID_818098406 A-to-I Human chr13 + 25096398 25096398 25096398 TGTGAACTTCCAGCATACGAAGGACGCGGAGCATGCTCTGGACACCATGAATTTTGATGTTATAA TGTGAACTTCCAGCATACGAAGGACGCGGAGCGTGCTCTGGACACCATGAATTTTGATGTTATAA A G PABPC3 Ensembl:ENSG00000151846 Protein coding CDS GSE38233 cultured B-cells chr13:25096397..25096398 24183664 RNA-Seq:(High) rs1269165434 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue 54204 RMVar_ID_54204 Human_SNP_ID_818159634 A-to-I Human chr13 - 110898757 110898757 110898757 GAGTGAAACTCCGTCTCAAAAAAAAAAAAAAAAAAAAAAGAAAAGAAAAACTAGTTGGGTATGGT GAGTGAAACTCCGTCTCAAAAAAAAAAAAAAAGAAAAAAGAAAAGAAAAACTAGTTGGGTATGGT T C ANKRD10,ANKRD10-IT1 Ensembl:ENSG00000088448,Ensembl:ENSG00000229152 Protein coding,lincRNA intron,intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line chr13:110898756..110898757 31158229 RNA-Seq:(High) rs1218075367 Functional Loss SNV ICGC 33..33 33 PBCA 2 - Human_RBP_ID_9752650,Human_RBP_ID_22913742,Human_RBP_ID_25076380 RMVar_hsa_circ_95018,RMVar_hsa_circ_164770,RMVar_hsa_circ_124905,RMVar_hsa_circ_164771,RMVar_hsa_circ_355791,RMVar_hsa_circ_164774 54205 RMVar_ID_54205 Human_SNP_ID_818177380 A-to-I Human chr13 - 30296412 30296412 30296412 TCAGGGGGCCCAAGCCTCCCTCCTTCCGGGGGATGTTAATCCAAGCCAGGTGGGTGAACTGAGAG TCAGGGGGCCCAAGCCTCCCTCCTTCCGGGGGGTGTTAATCCAAGCCAGGTGGGTGAACTGAGAG T C KATNAL1 Ensembl:ENSG00000102781 Protein coding intron GSE100210 HepG2 cell line chr13:30296411..30296412 29129909 RNA-Seq:(High) rs1438284894 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue 54206 RMVar_ID_54206 Human_SNP_ID_818182282 A-to-I Human chr13 - 21374439 21374439 21374439 CCTGAGGTCAGGGGTTCGAGATTAGCCTGGTCAAAATGGCAAAACCCTGTCTCCACTAAAAATAC CCTGAGGTCAGGGGTTCGAGATTAGCCTGGTCGAAATGGCAAAACCCTGTCTCCACTAAAAATAC T C ZDHHC20 Ensembl:ENSG00000180776 Protein coding 3'UTR GSE47997;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;esophageal squamous carcinoma cells,KYSE180 cell line chr13:21374438..21374439 23474544,32596459 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue Human_RBP_ID_26424827 RMVar_hsa_circ_82999,RMVar_hsa_circ_104322,RMVar_hsa_circ_112681,RMVar_hsa_circ_88460,RMVar_hsa_circ_162151,RMVar_hsa_circ_162153,RMVar_hsa_circ_162154,RMVar_hsa_circ_162152 54207 RMVar_ID_54207 Human_SNP_ID_818203866 A-to-I Human chr13 - 110685430 110685430 110685430 TTCCTGTCCTTCCTGGGTCCTACTTGGAGCGTAAGATGAGCACGTGAGGCCCTGAGGATCTGCTC TTCCTGTCCTTCCTGGGTCCTACTTGGAGCGTGAGATGAGCACGTGAGGCCCTGAGGATCTGCTC T C CARS2 Ensembl:ENSG00000134905 Protein coding intron GSE38233 cultured B-cells chr13:110685429..110685430 24183664 RNA-Seq:(High) rs4773237 Functional Loss SNV ICGC 33..33 33 LAML 1 - GWAS_ID_642,GWAS_ID_643,GWAS_ID_644,GWAS_ID_645,GWAS_ID_646,GWAS_ID_647,GWAS_ID_648,GWAS_ID_649,GWAS_ID_650 RMVar_hsa_circ_114303,RMVar_hsa_circ_164754,RMVar_hsa_circ_76335,RMVar_hsa_circ_164753,RMVar_hsa_circ_36728,RMVar_hsa_circ_40801,RMVar_hsa_circ_63373,RMVar_hsa_circ_367471,RMVar_hsa_circ_61249,RMVar_hsa_circ_58452,RMVar_hsa_circ_295262,RMVar_hsa_circ_312643,RMVar_hsa_circ_164760,RMVar_hsa_circ_164761,RMVar_hsa_circ_327531,RMVar_hsa_circ_109154,RMVar_hsa_circ_164765,RMVar_hsa_circ_164763,RMVar_hsa_circ_325567,RMVar_hsa_circ_326199,RMVar_hsa_circ_164764,RMVar_hsa_circ_301088,RMVar_hsa_circ_295564,RMVar_hsa_circ_347313 54208 RMVar_ID_54208 Human_SNP_ID_818312046 A-to-I Human chr13 - 90171129 90171129 90171129 CGCGCATTGTTCAAAGAATTCCTTTCCCTGCCACAATAAAGAGACCACTTGGTCCATTAAAGTTA CGCGCATTGTTCAAAGAATTCCTTTCCCTGCCGCAATAAAGAGACCACTTGGTCCATTAAAGTTA T C lnc-DCT-19 RNACentral:URS0000D5C80B lincRNA intron GSE100210 HepG2 cell line chr13:90171128..90171129 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 2 - 54209 RMVar_ID_54209 Human_SNP_ID_818498659 A-to-I Human chr13 + 45516235 45516235 45516235 GCTCCATTTCACACTGAATTCACCATTAAGGAAATTTCCCTGGACCTCAAGAAAACTAGAGGTAC GCTCCATTTCACACTGAATTCACCATTAAGGACATTTCCCTGGACCTCAAGAAAACTAGAGGTAC A C COG3 Ensembl:ENSG00000136152 Protein coding CDS GSE56152;GSE100210 embryonic stem cells,wild type;HepG2 cell line chr13:45516235..45516236 25708366,29129909 RNA-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 54210 RMVar_ID_54210 Human_SNP_ID_818582171 A-to-I Human chr13 - 32525038 32525038 32525038 ACTGGCATAGCTGGGTGCAGTGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCCGAGGCGGGC ACTGGCATAGCTGGGTGCAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGC T C N4BP2L2 Ensembl:ENSG00000244754 Protein coding intron GSE38233;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,KYSE180 cell line chr13:32525037..32525038 24183664,32596459 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 5 prostate Human_RBP_ID_118414,Human_RBP_ID_230519,Human_RBP_ID_9724984,Human_RBP_ID_12256919 RMVar_hsa_circ_16530,RMVar_hsa_circ_35673,RMVar_hsa_circ_162627,RMVar_hsa_circ_68852,RMVar_hsa_circ_101362,RMVar_hsa_circ_162639,RMVar_hsa_circ_162642,RMVar_hsa_circ_162645,RMVar_hsa_circ_279929,RMVar_hsa_circ_266394,RMVar_hsa_circ_374349,RMVar_hsa_circ_275780,RMVar_hsa_circ_162643,RMVar_hsa_circ_162644,RMVar_hsa_circ_162649,RMVar_hsa_circ_97693,RMVar_hsa_circ_286002,RMVar_hsa_circ_162648,RMVar_hsa_circ_311792 54211 RMVar_ID_54211 Human_SNP_ID_818590344 A-to-I Human chr13 + 25097436 25097436 25097436 CTTCATGACAGCTGTCCCACAGACTCAGAACCATGCTGCATACTATCCTCCTAGCCAAATTGCTC CTTCATGACAGCTGTCCCACAGACTCAGAACCGTGCTGCATACTATCCTCCTAGCCAAATTGCTC A G PABPC3 Ensembl:ENSG00000151846 Protein coding CDS GSE100210 HepG2 cell line chr13:25097435..25097436 29129909 RNA-Seq:(High) rs767843616 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 5 haematopoietic and lymphoid tissue Human_miRNA_ID_40970,Human_miRNA_ID_69690 54212 RMVar_ID_54212 Human_SNP_ID_818591833 A-to-I Human chr13 + 45031049 45031049 45031049 CTGGTGGCGGGTGCCTGTAATCCCAGCTACTCAGGAGGCTGAAGCAGGATAATTGCTTGAACCTA CTGGTGGCGGGTGCCTGTAATCCCAGCTACTCGGGAGGCTGAAGCAGGATAATTGCTTGAACCTA A G GPALPP1 Ensembl:ENSG00000133114 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line chr13:45031048..45031049 31158229 RNA-Seq:(High) rs1042385243 Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_163159 54213 RMVar_ID_54213 Human_SNP_ID_818593941 A-to-I Human chr13 - 110160877 110160877 110160877 TGACGAGACTTCATCTCCACAAAAAATACAAAAGTTAGCTGGGCGTGGTGGTGTGAGCCTGTGGT TGACGAGACTTCATCTCCACAAAAAATACAAACGTTAGCTGGGCGTGGTGGTGTGAGCCTGTGGT T G COL4A1 Ensembl:ENSG00000187498 Protein coding intron GSE100210 HepG2 cell line chr13:110160876..110160877 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_92341,RMVar_hsa_circ_164698 54214 RMVar_ID_54214 Human_SNP_ID_818604876 A-to-I Human chr13 - 95294806 95294806 95294806 GGGACTACAGATGTGCGCCACCATGCTCAGCTAATTTTTTGTACTTTTAGGAGAGATGGGGTTTC GGGACTACAGATGTGCGCCACCATGCTCAGCTGATTTTTTGTACTTTTAGGAGAGATGGGGTTTC T C ABCC4 Ensembl:ENSG00000125257 Protein coding intron GSE100210 HepG2 cell line chr13:95294805..95294806 29129909 RNA-Seq:(High) rs541735957 Functional Loss SNV ICGC 33..33 33 MALY 1 - RMVar_hsa_circ_95851,RMVar_hsa_circ_164104,RMVar_hsa_circ_81497,RMVar_hsa_circ_164125 54215 RMVar_ID_54215 Human_SNP_ID_818635510 A-to-I Human chr13 - 41663761 41663761 41663761 ATGTAGAAAAATTGTTAAATTGAATCATCGTAAGTCGGGGACTGTATAGTAATGATAAGGTAAAC ATGTAGAAAAATTGTTAAATTGAATCATCGTACGTCGGGGACTGTATAGTAATGATAAGGTAAAC T G VWA8 Ensembl:ENSG00000102763 Protein coding intron GSE100210 HepG2 cell line chr13:41663760..41663761 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 2 oesophagus RMVar_hsa_circ_944,RMVar_hsa_circ_80270,RMVar_hsa_circ_89747,RMVar_hsa_circ_162981,RMVar_hsa_circ_114104,RMVar_hsa_circ_62871,RMVar_hsa_circ_5723,RMVar_hsa_circ_33679,RMVar_hsa_circ_97332,RMVar_hsa_circ_162982,RMVar_hsa_circ_162983,RMVar_hsa_circ_58305,RMVar_hsa_circ_95405,RMVar_hsa_circ_104971,RMVar_hsa_circ_162984,RMVar_hsa_circ_162985,RMVar_hsa_circ_162986,RMVar_hsa_circ_125325,RMVar_hsa_circ_58179,RMVar_hsa_circ_162987,RMVar_hsa_circ_108630,RMVar_hsa_circ_100299,RMVar_hsa_circ_162988,RMVar_hsa_circ_162989 54216 RMVar_ID_54216 Human_SNP_ID_818717499 A-to-I Human chr13 - 30296407 30296407 30296407 GGGCCCAAGCCTCCCTCCTTCCGGGGGATGTTAATCCAAGCCAGGTGGGTGAACTGAGAGTCCAC GGGCCCAAGCCTCCCTCCTTCCGGGGGATGTTGATCCAAGCCAGGTGGGTGAACTGAGAGTCCAC T C KATNAL1 Ensembl:ENSG00000102781 Protein coding intron GSE100210 HepG2 cell line chr13:30296406..30296407 29129909 RNA-Seq:(High) rs1158446626 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue 54217 RMVar_ID_54217 Human_SNP_ID_818783330 A-to-I Human chr13 + 25098050 25098050 25098050 CTGTACTACAAGCCCACCAAGCTAAAGAGGCTACCCAGAAAGCAGTTAACAGTGCTACCGGTGTT CTGTACTACAAGCCCACCAAGCTAAAGAGGCTTCCCAGAAAGCAGTTAACAGTGCTACCGGTGTT A T PABPC3 Ensembl:ENSG00000151846 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr13:25098049..25098050 30559470 RNA-Seq:(High) rs999778271 Functional Loss SNV ICGC 33..33 33 COCA 1 - 54218 RMVar_ID_54218 Human_SNP_ID_818783379 A-to-I Human chr13 + 25098050 25098050 25098050 CTGTACTACAAGCCCACCAAGCTAAAGAGGCTACCCAGAAAGCAGTTAACAGTGCTACCGGTGTT CTGTACTACAAGCCCACCAAGCTAAAGAGGCTGCCCAGAAAGCAGTTAACAGTGCTACCGGTGTT A G PABPC3 Ensembl:ENSG00000151846 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr13:25098049..25098050 30559470 RNA-Seq:(High) rs999778271 Functional Loss SNV ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LICA,liver neoplasm,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 5 lung,liver,haematopoietic and lymphoid tissue 54219 RMVar_ID_54219 Human_SNP_ID_818800231 A-to-I Human chr13 - 21375058 21375057 21375058 GGGATCTTGGCTCGCTGCAACCTCTGCCTTCCAGGTTCAATAGAGTCTCCTGCCTCAGCCTCCCA GGGATCTTGGCTCGCTGCAACCTCTGCCTTCC_GGTTCAATAGAGTCTCCTGCCTCAGCCTCCCA CT C ZDHHC20 Ensembl:ENSG00000180776 Protein coding 3'UTR GSE112787;GSE123020:GSM3490832,GSM3490833,GSM3490834 293 Flip-In T-REx cells,empty vector;esophageal squamous carcinoma cells,KYSE180 cell line chr13:21375057..21375058 29967493,32596459 RNA-Seq:(High) - Functional Loss DEL ICGC 33..33 33 NKTL 1 - RMVar_hsa_circ_82999,RMVar_hsa_circ_104322,RMVar_hsa_circ_112681,RMVar_hsa_circ_88460,RMVar_hsa_circ_162151,RMVar_hsa_circ_162153,RMVar_hsa_circ_162154,RMVar_hsa_circ_162152 54220 RMVar_ID_54220 Human_SNP_ID_818805980 A-to-I Human chr13 - 107759403 107759403 107759403 GAGATGGAGACCATCCTGGCTAACATGGTGAAACCCCGCCTCTACTAAAAATACTAAAAATTATC GAGATGGAGACCATCCTGGCTAACATGGTGAACCCCCGCCTCTACTAAAAATACTAAAAATTATC T G FAM155A Ensembl:ENSG00000204442 Protein coding intron GSE47997 K562 cells&HepG2 cells chr13:107759402..107759403 23474544 RNA-Seq:(High) rs929565279 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 54221 RMVar_ID_54221 Human_SNP_ID_818815985 A-to-I Human chr13 + 102841436 102841436 102841436 TTTTTCTGAAGAGAATATTTTGCTTGAAATGCAAAGGACTGAAAGAGATTTGTAGGTTGTTGATT TTTTTCTGAAGAGAATATTTTGCTTGAAATGCGAAGGACTGAAAGAGATTTGTAGGTTGTTGATT A G ERCC5,BIVM-ERCC5,BIVM Ensembl:ENSG00000134899,Ensembl:ENSG00000270181,Ensembl:ENSG00000134897 Protein coding,Protein coding,Protein coding intron,intron,3'UTR GSE100210 HepG2 cell line chr13:102841436..102841437 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_1804365,Human_RBP_ID_18266240,Human_RBP_ID_23584128 RMVar_hsa_circ_164592,RMVar_hsa_circ_97419,RMVar_hsa_circ_91981,RMVar_hsa_circ_164604,RMVar_hsa_circ_86825,RMVar_hsa_circ_164606,RMVar_hsa_circ_82387,RMVar_hsa_circ_104044,RMVar_hsa_circ_164609,RMVar_hsa_circ_164610 54222 RMVar_ID_54222 Human_SNP_ID_818870098 A-to-I Human chr13 - 21374486 21374486 21374486 TCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCTGGCGGATCACCTGAGGTCAGGGGTTCG TCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCTGGCGGATCACCTGAGGTCAGGGGTTCG T C ZDHHC20 Ensembl:ENSG00000180776 Protein coding 3'UTR GSE38233;GSE112787;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;293 Flip-In T-REx cells,empty vector;esophageal squamous carcinoma cells,KYSE180 cell line chr13:21374485..21374486 24183664,29967493,32596459 RNA-Seq:(High) rs1411282817 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue RMVar_hsa_circ_82999,RMVar_hsa_circ_104322,RMVar_hsa_circ_112681,RMVar_hsa_circ_88460,RMVar_hsa_circ_162151,RMVar_hsa_circ_162153,RMVar_hsa_circ_162154,RMVar_hsa_circ_162152 54223 RMVar_ID_54223 Human_SNP_ID_819014993 A-to-I Human chr13 - 21628657 21628657 21628657 TACAAAAAATAAGCAAAAGCGTCCCAGGAGCCATACTCTGACAGCTGTGCACGATGCCATCCTTG TACAAAAAATAAGCAAAAGCGTCCCAGGAGCCGTACTCTGACAGCTGTGCACGATGCCATCCTTG T C RPS7P10 Ensembl:ENSG00000226525 Pseudogene exon GSE100210 HepG2 cell line chr13:21628656..21628657 29129909 RNA-Seq:(High) rs747280665 Functional Loss SNV ICGC 33..33 33 LICA 2 - Human_RBP_ID_433264,Human_RBP_ID_17361117 Human_miRNA_ID_1887709,Human_miRNA_ID_1887753,Human_miRNA_ID_1887797 54224 RMVar_ID_54224 Human_SNP_ID_819037477 A-to-I Human chr13 - 25097966 25097966 25097966 AGAACGGAGTGACTCTGGAGACTCGAGCATATAAAGAAGTTCTGAATTATCAATCTCCAACAACA AGAACGGAGTGACTCTGGAGACTCGAGCATATGAAGAAGTTCTGAATTATCAATCTCCAACAACA T C - - Other Unknown GSE107867 ASD brains,cerebellum chr13:25097965..25097966 30559470 RNA-Seq:(High) rs779122561 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma,lung non_small_cell_carcinoma,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 lung,haematopoietic and lymphoid tissue 54225 RMVar_ID_54225 Human_SNP_ID_819079701 A-to-I Human chr13 + 49486253 49486253 49486253 TTGAGGTCAGGAGTTTGAGGTTACAGTGAACTATGATTGTGCCACGGTACTGCAGCCTGGGCGAT TTGAGGTCAGGAGTTTGAGGTTACAGTGAACTTTGATTGTGCCACGGTACTGCAGCCTGGGCGAT A T SETDB2 Ensembl:ENSG00000136169 Protein coding intron GSE100210 HepG2 cell line chr13:49486252..49486253 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - RMVar_hsa_circ_266810,RMVar_hsa_circ_302348,RMVar_hsa_circ_65228,RMVar_hsa_circ_163373,RMVar_hsa_circ_294078,RMVar_hsa_circ_163383,RMVar_hsa_circ_357210,RMVar_hsa_circ_163386,RMVar_hsa_circ_327421 54226 RMVar_ID_54226 Human_SNP_ID_819108536 A-to-I Human chr13 + 47763633 47763633 47763633 CTTGCAGCCCTTCAAGAAAGACTTGATGGTCTAATAGAAACACCAACAGGATACATTGAAAGCCT CTTGCAGCCCTTCAAGAAAGACTTGATGGTCTGATAGAAACACCAACAGGATACATTGAAAGCCT A G NAP1L4P3 Ensembl:ENSG00000234145 Pseudogene exon GSE100210 HepG2 cell line chr13:47763632..47763633;chr13:47763633..47763634 29129909 RNA-Seq:(High) rs1032451635 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_6314927 54227 RMVar_ID_54227 Human_SNP_ID_819147609 A-to-I Human chr13 - 21374438 21374438 21374438 CTGAGGTCAGGGGTTCGAGATTAGCCTGGTCAAAATGGCAAAACCCTGTCTCCACTAAAAATACA CTGAGGTCAGGGGTTCGAGATTAGCCTGGTCAGAATGGCAAAACCCTGTCTCCACTAAAAATACA T C ZDHHC20 Ensembl:ENSG00000180776 Protein coding 3'UTR GSE47997;GSE38233;GSE99789;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;esophageal squamous carcinoma cells,EC109;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,KYSE180 cell line chr13:21374437..21374438 23474544,24183664,29796672,30559470,31158229,31158229,32596459 RNA-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_26424827 RMVar_hsa_circ_82999,RMVar_hsa_circ_104322,RMVar_hsa_circ_112681,RMVar_hsa_circ_88460,RMVar_hsa_circ_162151,RMVar_hsa_circ_162153,RMVar_hsa_circ_162154,RMVar_hsa_circ_162152 54228 RMVar_ID_54228 Human_SNP_ID_819149392 A-to-I Human chr13 - 21374516 21374516 21374516 GAGATACCAATTATTGCTGGGTGTGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAG GAGATACCAATTATTGCTGGGTGTGGTGGCTCGTGCCTGTAATCCCAGCACTTTGGGAGGCCAAG T C ZDHHC20 Ensembl:ENSG00000180776 Protein coding 3'UTR GSE38233;GSE99789;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,EC109;esophageal squamous carcinoma cells,KYSE180 cell line chr13:21374515..21374516 24183664,29796672,32596459 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue RMVar_hsa_circ_82999,RMVar_hsa_circ_104322,RMVar_hsa_circ_112681,RMVar_hsa_circ_88460,RMVar_hsa_circ_162151,RMVar_hsa_circ_162153,RMVar_hsa_circ_162154,RMVar_hsa_circ_162152 54229 RMVar_ID_54229 Human_SNP_ID_819162761 A-to-I Human chr13 - 49668389 49668389 49668389 TTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTAGCCAGGATGGTCTCGATCTCCTGACCT TTTTGTATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGGTCTCGATCTCCTGACCT T C EBPL Ensembl:ENSG00000123179 Protein coding intron GSE47997 K562 cells&HepG2 cells chr13:49668388..49668389 23474544 RNA-Seq:(High) rs180838292 Functional Loss SNV ICGC 33..33 33 COCA 1 - Human_RBP_ID_118729 54230 RMVar_ID_54230 Human_SNP_ID_819199161 A-to-I Human chr13 - 33829993 33829993 33829993 TGACCTACATCTTCAATGCTGGGAGCAGGCACACGAACCGCCAAGCACCTACTACGAATAGGTGG TGACCTACATCTTCAATGCTGGGAGCAGGCACCCGAACCGCCAAGCACCTACTACGAATAGGTGG T G - - Other Unknown GSE38233 cultured B-cells chr13:33829993..33829994 24183664 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 STAD,stomach adenocarcinoma 4 stomach 54231 RMVar_ID_54231 Human_SNP_ID_819238053 A-to-I Human chr13 - 95079766 95079766 95079766 AGTGGCCGTGATCTTGGGTCACTGCAACTTCCACCTCCCGAGTTCAAGAAATTCTCCTGTCTCAG AGTGGCCGTGATCTTGGGTCACTGCAACTTCCCCCTCCCGAGTTCAAGAAATTCTCCTGTCTCAG T G ABCC4 Ensembl:ENSG00000125257 Protein coding intron GSE100210 HepG2 cell line chr13:95079765..95079766 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - RMVar_hsa_circ_4275,RMVar_hsa_circ_24477,RMVar_hsa_circ_111278,RMVar_hsa_circ_164070,RMVar_hsa_circ_287831,RMVar_hsa_circ_301609,RMVar_hsa_circ_85056,RMVar_hsa_circ_164075,RMVar_hsa_circ_164076,RMVar_hsa_circ_336783,RMVar_hsa_circ_55212,RMVar_hsa_circ_37691,RMVar_hsa_circ_49829,RMVar_hsa_circ_96604,RMVar_hsa_circ_164080,RMVar_hsa_circ_104423,RMVar_hsa_circ_304510,RMVar_hsa_circ_164081,RMVar_hsa_circ_112648,RMVar_hsa_circ_164082,RMVar_hsa_circ_164083,RMVar_hsa_circ_35420,RMVar_hsa_circ_298307,RMVar_hsa_circ_305570,RMVar_hsa_circ_377454,RMVar_hsa_circ_94694,RMVar_hsa_circ_164084,RMVar_hsa_circ_341527,RMVar_hsa_circ_13685,RMVar_hsa_circ_164086,RMVar_hsa_circ_342367 54232 RMVar_ID_54232 Human_SNP_ID_819335688 A-to-I Human chr13 + 78909891 78909891 78909891 ACTTCTTCAGAACAACTTGCCTGCGGTTTGCTAGGTAGGAGGACCTGAAATTGAACTGATTGCCA ACTTCTTCAGAACAACTTGCCTGCGGTTTGCTGGGTAGGAGGACCTGAAATTGAACTGATTGCCA A G CCT5P2 Ensembl:ENSG00000230584 Pseudogene exon GSE100210 HepG2 cell line chr13:78909890..78909891 29129909 RNA-Seq:(High) rs1417558050 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_4274685 54233 RMVar_ID_54233 Human_SNP_ID_819377762 A-to-I Human chr13 + 97291815 97291815 97291815 TACTCAGGAGGCTGAGGCAGGAGAATCGCTTGAACCTGGGAGGCGGAGGTTGCAGTGAGCTGAGA TACTCAGGAGGCTGAGGCAGGAGAATCGCTTGTACCTGGGAGGCGGAGGTTGCAGTGAGCTGAGA A T MBNL2 Ensembl:ENSG00000139793 Protein coding intron GSE47997 K562 cells&HepG2 cells chr13:97291815..97291816 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 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 54234 RMVar_ID_54234 Human_SNP_ID_819435183 A-to-I Human chr13 - 98506937 98506937 98506937 CAGTGAGGTTCCCCTGAAAGCCTGAGCAAATTAGCAAGACGGGCCTGCGGGCTCCTGGCCCAGGG CAGTGAGGTTCCCCTGAAAGCCTGAGCAAATTGGCAAGACGGGCCTGCGGGCTCCTGGCCCAGGG T C STK24 Ensembl:ENSG00000102572 Protein coding intron GSE100210 HepG2 cell line chr13:98506936..98506937 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - RMVar_hsa_circ_351090,RMVar_hsa_circ_73968,RMVar_hsa_circ_34426,RMVar_hsa_circ_164333,RMVar_hsa_circ_273643,RMVar_hsa_circ_164334,RMVar_hsa_circ_99478,RMVar_hsa_circ_351663 54235 RMVar_ID_54235 Human_SNP_ID_819459085 A-to-I Human chr13 + 52460963 52460963 52460963 AAGTTCAAGAAGGGACTAAAGTGCTGAAACTTAAAACAAAAATGGTAAGATGTGGACATAGCACT AAGTTCAAGAAGGGACTAAAGTGCTGAAACTTGAAACAAAAATGGTAAGATGTGGACATAGCACT A G CKAP2 Ensembl:ENSG00000136108 Protein coding intron GSE100210 HepG2 cell line chr13:52460963..52460964 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 4 large intestine Human_RBP_ID_1485523,Human_RBP_ID_1811015,Human_RBP_ID_6295231,Human_RBP_ID_8393910,Human_RBP_ID_9367558,Human_RBP_ID_12189232,Human_RBP_ID_18435333,Human_RBP_ID_27807962 Human_Splice_Rec_1468692,Human_Splice_Rec_1468693,Human_Splice_Rec_1468702,Human_Splice_Rec_1468703,Human_Splice_Rec_1468718,Human_Splice_Rec_1468719,Human_Splice_Rec_1468734,Human_Splice_Rec_1468735,Human_Splice_Rec_1468750,Human_Splice_Rec_1468751 RMVar_hsa_circ_357563,RMVar_hsa_circ_58668,RMVar_hsa_circ_358891,RMVar_hsa_circ_366781,RMVar_hsa_circ_347706,RMVar_hsa_circ_357975,RMVar_hsa_circ_288085 54236 RMVar_ID_54236 Human_SNP_ID_819515504 A-to-I Human chr13 - 77187009 77187009 77187009 GCTCAGGAGTTCAAGACCAGCCAGGGCAATATAGTGAAACCCCCATCTAAAAAAACTTAAAAATT GCTCAGGAGTTCAAGACCAGCCAGGGCAATATGGTGAAACCCCCATCTAAAAAAACTTAAAAATT T C MYCBP2 Ensembl:ENSG00000005810 Protein coding intron GSE38233 cultured B-cells chr13:77187008..77187009 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 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_111742,RMVar_hsa_circ_163829,RMVar_hsa_circ_124062,RMVar_hsa_circ_163841,RMVar_hsa_circ_109703,RMVar_hsa_circ_163845,RMVar_hsa_circ_354598,RMVar_hsa_circ_100693,RMVar_hsa_circ_163851,RMVar_hsa_circ_94635,RMVar_hsa_circ_113731,RMVar_hsa_circ_120994,RMVar_hsa_circ_163855,RMVar_hsa_circ_103365,RMVar_hsa_circ_42233,RMVar_hsa_circ_78772,RMVar_hsa_circ_92922,RMVar_hsa_circ_47374,RMVar_hsa_circ_30165,RMVar_hsa_circ_11126,RMVar_hsa_circ_163857,RMVar_hsa_circ_163861,RMVar_hsa_circ_163859,RMVar_hsa_circ_163860,RMVar_hsa_circ_163858,RMVar_hsa_circ_82867,RMVar_hsa_circ_100744,RMVar_hsa_circ_163871,RMVar_hsa_circ_49272,RMVar_hsa_circ_163873,RMVar_hsa_circ_118177,RMVar_hsa_circ_25167,RMVar_hsa_circ_163875,RMVar_hsa_circ_29960,RMVar_hsa_circ_89696,RMVar_hsa_circ_163880,RMVar_hsa_circ_9375,RMVar_hsa_circ_32270,RMVar_hsa_circ_163883,RMVar_hsa_circ_53233,RMVar_hsa_circ_75091,RMVar_hsa_circ_163885,RMVar_hsa_circ_17100,RMVar_hsa_circ_108512,RMVar_hsa_circ_40550,RMVar_hsa_circ_98933,RMVar_hsa_circ_93400,RMVar_hsa_circ_19440,RMVar_hsa_circ_163889,RMVar_hsa_circ_266522,RMVar_hsa_circ_163890,RMVar_hsa_circ_163892,RMVar_hsa_circ_76077,RMVar_hsa_circ_163891 54237 RMVar_ID_54237 Human_SNP_ID_819548076 A-to-I Human chr13 - 21374508 21374508 21374508 AATTATTGCTGGGTGTGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCTGGCGG AATTATTGCTGGGTGTGGTGGCTCATGCCTGTGATCCCAGCACTTTGGGAGGCCAAGGCTGGCGG T C ZDHHC20 Ensembl:ENSG00000180776 Protein coding 3'UTR GSE38233 cultured B-cells chr13:21374507..21374508 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue RMVar_hsa_circ_82999,RMVar_hsa_circ_104322,RMVar_hsa_circ_112681,RMVar_hsa_circ_88460,RMVar_hsa_circ_162151,RMVar_hsa_circ_162153,RMVar_hsa_circ_162154,RMVar_hsa_circ_162152 54238 RMVar_ID_54238 Human_SNP_ID_819560813 A-to-I Human chr13 - 66585207 66585207 66585207 ATAAAAATTCTCTTCAGAAAAATAATGCATATATGCATTTAATAAAATAAATAAATGCATGCACC ATAAAAATTCTCTTCAGAAAAATAATGCATATGTGCATTTAATAAAATAAATAAATGCATGCACC T C PCDH9 Ensembl:ENSG00000184226 Protein coding intron GSE107867 ASD brains,frontal_cortex chr13:66585206..66585207 30559470 RNA-Seq:(High) rs958155271 Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_96620,RMVar_hsa_circ_163640 54239 RMVar_ID_54239 Human_SNP_ID_819622876 A-to-I Human chr13 - 25096402 25096402 25096402 CCCTTTATAACATCAAAATTCATGGTGTCCAGAGCATGCTCCGCGTCCTTCGTATGCTGGAAGTT CCCTTTATAACATCAAAATTCATGGTGTCCAGGGCATGCTCCGCGTCCTTCGTATGCTGGAAGTT T C - - Other Unknown GSE38233 cultured B-cells chr13:25096402..25096403 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 2 pancreas 54240 RMVar_ID_54240 Human_SNP_ID_819674794 A-to-I Human chr13 - 18892485 18892485 18892485 CTGGCTGCTGAGAAACAGGCTTTGCAGAGCCTAATGGGAGTCCTCCCAGATCTCATAGTAGAAAT CTGGCTGCTGAGAAACAGGCTTTGCAGAGCCTGATGGGAGTCCTCCCAGATCTCATAGTAGAAAT T C SNX19P2 Ensembl:ENSG00000235500 Pseudogene exon GSE100210 HepG2 cell line chr13:18892484..18892485 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 2 - 54241 RMVar_ID_54241 Human_SNP_ID_819742536 A-to-I Human chr13 + 28187891 28187891 28187891 AATTTTTTAAATTCTTGTGGAGACTGGGTCTCACTCTGTTGCCCAGGCTGGTCTTGAACTCCTGG AATTTTTTAAATTCTTGTGGAGACTGGGTCTCGCTCTGTTGCCCAGGCTGGTCTTGAACTCCTGG A G PAN3 Ensembl:ENSG00000152520 Protein coding intron GSE100210 HepG2 cell line chr13:28187890..28187891 29129909 RNA-Seq:(High) rs970678683 Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_49856,RMVar_hsa_circ_88548,RMVar_hsa_circ_127771,RMVar_hsa_circ_162417,RMVar_hsa_circ_76164,RMVar_hsa_circ_114856,RMVar_hsa_circ_110149,RMVar_hsa_circ_162418,RMVar_hsa_circ_162419,RMVar_hsa_circ_309106,RMVar_hsa_circ_339660,RMVar_hsa_circ_295667,RMVar_hsa_circ_270128,RMVar_hsa_circ_162421,RMVar_hsa_circ_162425,RMVar_hsa_circ_50550,RMVar_hsa_circ_122980,RMVar_hsa_circ_162426,RMVar_hsa_circ_162423,RMVar_hsa_circ_162424,RMVar_hsa_circ_162422,RMVar_hsa_circ_93674,RMVar_hsa_circ_337001,RMVar_hsa_circ_117709,RMVar_hsa_circ_90916,RMVar_hsa_circ_162431,RMVar_hsa_circ_162433,RMVar_hsa_circ_162435,RMVar_hsa_circ_162434,RMVar_hsa_circ_162432,RMVar_hsa_circ_115771,RMVar_hsa_circ_96660,RMVar_hsa_circ_162437,RMVar_hsa_circ_14598,RMVar_hsa_circ_162436 54242 RMVar_ID_54242 Human_SNP_ID_819747645 A-to-I Human chr13 - 21375058 21375058 21375058 GGGATCTTGGCTCGCTGCAACCTCTGCCTTCCAGGTTCAATAGAGTCTCCTGCCTCAGCCTCCCA GGGATCTTGGCTCGCTGCAACCTCTGCCTTCCGGGTTCAATAGAGTCTCCTGCCTCAGCCTCCCA T C ZDHHC20 Ensembl:ENSG00000180776 Protein coding 3'UTR GSE112787;GSE123020:GSM3490832,GSM3490833,GSM3490834 293 Flip-In T-REx cells,empty vector;esophageal squamous carcinoma cells,KYSE180 cell line chr13:21375057..21375058 29967493,32596459 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue RMVar_hsa_circ_82999,RMVar_hsa_circ_104322,RMVar_hsa_circ_112681,RMVar_hsa_circ_88460,RMVar_hsa_circ_162151,RMVar_hsa_circ_162153,RMVar_hsa_circ_162154,RMVar_hsa_circ_162152 54243 RMVar_ID_54243 Human_SNP_ID_819771253 A-to-I Human chr13 - 21374353 21374353 21374353 AGGCATGGTGGCACACGCCTGTAGTCCCAACTACTCGGGAGGTGGAGGCAGGAGAATCACTTGAA AGGCATGGTGGCACACGCCTGTAGTCCCAACTGCTCGGGAGGTGGAGGCAGGAGAATCACTTGAA T C ZDHHC20 Ensembl:ENSG00000180776 Protein coding 3'UTR GSE47997;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829 K562 cells&HepG2 cells;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line chr13:21374352..21374353 23474544,29796672,31158229 RNA-Seq:(High) rs1391495444 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue Human_RBP_ID_118323,Human_RBP_ID_4265531,Human_RBP_ID_23306400,Human_RBP_ID_26424825 RMVar_hsa_circ_82999,RMVar_hsa_circ_104322,RMVar_hsa_circ_112681,RMVar_hsa_circ_88460,RMVar_hsa_circ_162151,RMVar_hsa_circ_162153,RMVar_hsa_circ_162154,RMVar_hsa_circ_162152 54244 RMVar_ID_54244 Human_SNP_ID_819800907 A-to-I Human chr13 - 21374431 21374431 21374431 CAGGGGTTCGAGATTAGCCTGGTCAAAATGGCAAAACCCTGTCTCCACTAAAAATACAAAAAAAC CAGGGGTTCGAGATTAGCCTGGTCAAAATGGCGAAACCCTGTCTCCACTAAAAATACAAAAAAAC T C ZDHHC20 Ensembl:ENSG00000180776 Protein coding 3'UTR GSE47997;GSE38233;GSE112787 K562 cells&HepG2 cells;cultured B-cells;293 Flip-In T-REx cells,empty vector chr13:21374430..21374431 23474544,24183664,29967493 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue Human_RBP_ID_26424827,Human_RBP_ID_27426998 RMVar_hsa_circ_82999,RMVar_hsa_circ_104322,RMVar_hsa_circ_112681,RMVar_hsa_circ_88460,RMVar_hsa_circ_162151,RMVar_hsa_circ_162153,RMVar_hsa_circ_162154,RMVar_hsa_circ_162152 54245 RMVar_ID_54245 Human_SNP_ID_819834072 A-to-I Human chr13 - 30356838 30356838 30356838 TAGCTCCTGGGCTCAAGCAATCTGCCTGCCTCAGCCTCCCAGAGGCCTGGAACTACAGGCGTGAG TAGCTCCTGGGCTCAAGCAATCTGCCTGCCTCGGCCTCCCAGAGGCCTGGAACTACAGGCGTGAG T C LINC00426 Ensembl:ENSG00000238121 lincRNA intron GSE38233 cultured B-cells chr13:30356837..30356838 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 COCA 1 - 54246 RMVar_ID_54246 Human_SNP_ID_819904385 A-to-I Human chr13 + 52030744 52030744 52030744 GGGCCTAAAGCCCAGTGCCAAGAAAAGACGCCAGTTTCTCATTAAAGCCCCTGAGGGTCCTCCAA GGGCCTAAAGCCCAGTGCCAAGAAAAGACGCCGGTTTCTCATTAAAGCCCCTGAGGGTCCTCCAA A G ALG11,UTP14C Ensembl:ENSG00000253710,Ensembl:ENSG00000253797 Protein coding,Protein coding 3'UTR,CDS GSE100210 HepG2 cell line chr13:52030743..52030744 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue 54247 RMVar_ID_54247 Human_SNP_ID_820002618 A-to-I Human chr13 - 21374356 21374356 21374356 TCCAGGCATGGTGGCACACGCCTGTAGTCCCAACTACTCGGGAGGTGGAGGCAGGAGAATCACTT TCCAGGCATGGTGGCACACGCCTGTAGTCCCAGCTACTCGGGAGGTGGAGGCAGGAGAATCACTT T C ZDHHC20 Ensembl:ENSG00000180776 Protein coding 3'UTR GSE47997;GSE38233;GSE112787;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE123020:GSM3490832,GSM3490833,GSM3490834 K562 cells&HepG2 cells;cultured B-cells;293 Flip-In T-REx cells,empty vector;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;esophageal squamous carcinoma cells,KYSE180 cell line chr13:21374355..21374356 23474544,24183664,29967493,31158229,31158229,32596459 RNA-Seq:(High) rs1282877635 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue Human_RBP_ID_118323,Human_RBP_ID_23306400,Human_RBP_ID_26424825 RMVar_hsa_circ_82999,RMVar_hsa_circ_104322,RMVar_hsa_circ_112681,RMVar_hsa_circ_88460,RMVar_hsa_circ_162151,RMVar_hsa_circ_162153,RMVar_hsa_circ_162154,RMVar_hsa_circ_162152 54248 RMVar_ID_54248 Human_SNP_ID_820044792 A-to-I Human chr13 - 102064201 102064201 102064201 AGGCATAAAACTGGGACAGAAAATACTGTCCAAGTTTTATGCCTGGTGGTACCTTAGTTCTTTTC AGGCATAAAACTGGGACAGAAAATACTGTCCACGTTTTATGCCTGGTGGTACCTTAGTTCTTTTC T G FGF14 Ensembl:ENSG00000102466 Protein coding intron GSE107867 ASD brains,frontal_cortex chr13:102064200..102064201 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 2 - RMVar_hsa_circ_280140 54249 RMVar_ID_54249 Human_SNP_ID_820057897 A-to-I Human chr13 + 32684000 32684000 32684000 TTCTGGTCAATGATCACTTACTTAATTTTGTGAGAGAGAGAACATTAGACAAACGAGTAAGTATG TTCTGGTCAATGATCACTTACTTAATTTTGTGTGAGAGAGAACATTAGACAAACGAGTAAGTATG A T PDS5B Ensembl:ENSG00000083642 Protein coding CDS GSE100210 HepG2 cell line chr13:32683999..32684000 29129909 RNA-Seq:(High) rs750827034 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,BRCA,STAD,stomach adenocarcinoma,colon adenocarcinoma,caecum adenocarcinoma,UCEC,large_intestine adenocarcinoma,endometrium endometrioid_carcinoma 19 caecum,uterus,stomach,large intestine Human_RBP_ID_12137303 Human_Splice_Rec_1455459,Human_Splice_Rec_1455529,Human_Splice_Rec_1455551 RMVar_hsa_circ_506,RMVar_hsa_circ_32585,RMVar_hsa_circ_162656,RMVar_hsa_circ_334771,RMVar_hsa_circ_354316,RMVar_hsa_circ_375788,RMVar_hsa_circ_162655,RMVar_hsa_circ_340371,RMVar_hsa_circ_307948,RMVar_hsa_circ_323421,RMVar_hsa_circ_274851,RMVar_hsa_circ_42659,RMVar_hsa_circ_162662,RMVar_hsa_circ_162663,RMVar_hsa_circ_162661,RMVar_hsa_circ_336933,RMVar_hsa_circ_319512,RMVar_hsa_circ_47325,RMVar_hsa_circ_83008,RMVar_hsa_circ_12629,RMVar_hsa_circ_26125,RMVar_hsa_circ_162665,RMVar_hsa_circ_162666,RMVar_hsa_circ_162664,RMVar_hsa_circ_162670,RMVar_hsa_circ_11142,RMVar_hsa_circ_1730,RMVar_hsa_circ_11295,RMVar_hsa_circ_13352,RMVar_hsa_circ_16800,RMVar_hsa_circ_6430,RMVar_hsa_circ_312531,RMVar_hsa_circ_348095,RMVar_hsa_circ_366649,RMVar_hsa_circ_345176,RMVar_hsa_circ_41627,RMVar_hsa_circ_66982,RMVar_hsa_circ_38471,RMVar_hsa_circ_62706,RMVar_hsa_circ_162673,RMVar_hsa_circ_162674,RMVar_hsa_circ_126623,RMVar_hsa_circ_162676,RMVar_hsa_circ_38159,RMVar_hsa_circ_162675,RMVar_hsa_circ_311093,RMVar_hsa_circ_336662,RMVar_hsa_circ_162677,RMVar_hsa_circ_41772,RMVar_hsa_circ_313993,RMVar_hsa_circ_316841,RMVar_hsa_circ_44434,RMVar_hsa_circ_37225,RMVar_hsa_circ_162678 54250 RMVar_ID_54250 Human_SNP_ID_820063957 A-to-I Human chr13 - 110938898 110938898 110938898 GGATCTGAGAGTCGCTGCTGCCCTGGGACACCACCTGCTGGACCTGAGGATGGAGTACGCGGCCT GGATCTGAGAGTCGCTGCTGCCCTGGGACACCGCCTGCTGGACCTGAGGATGGAGTACGCGGCCT T C - - Other Unknown GSE100210 HepG2 cell line chr13:110938897..110938898 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 54251 RMVar_ID_54251 Human_SNP_ID_820079950 A-to-I Human chr13 - 77001106 77001106 77001106 TCTTTACAAGAGAAGAGTCCTGAGATGTTAATATGCAGCAATTCTGCTGATGTGCATTTTAACTT TCTTTACAAGAGAAGAGTCCTGAGATGTTAATGTGCAGCAATTCTGCTGATGTGCATTTTAACTT T C FBXL3 Ensembl:ENSG00000005812 Protein coding intron GSE100210 HepG2 cell line chr13:77001105..77001106 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_439187,Human_RBP_ID_12219509 54252 RMVar_ID_54252 Human_SNP_ID_820088071 A-to-I Human chr13 - 18892463 18892463 18892463 TGCAGAGCCTAATGGGAGTCCTCCCAGATCTCATAGTAGAAATTCTTGGGGTGAACAAATGCCAG TGCAGAGCCTAATGGGAGTCCTCCCAGATCTCGTAGTAGAAATTCTTGGGGTGAACAAATGCCAG T C SNX19P2 Ensembl:ENSG00000235500 Pseudogene exon GSE100210 HepG2 cell line chr13:18892462..18892463 29129909 RNA-Seq:(High) rs1256524675 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_8249089 54253 RMVar_ID_54253 Human_SNP_ID_820158837 A-to-I Human chr13 - 110898920 110898920 110898920 AAACCCCGTCTCTACTAAAAATACAAAAAATTAGCTGGGTGTGGTGGTGGGCGCTTGTAATACCA AAACCCCGTCTCTACTAAAAATACAAAAAATTTGCTGGGTGTGGTGGTGGGCGCTTGTAATACCA T A ANKRD10,ANKRD10-IT1 Ensembl:ENSG00000088448,Ensembl:ENSG00000229152 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line chr13:110898919..110898920 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_95018,RMVar_hsa_circ_164770,RMVar_hsa_circ_124905,RMVar_hsa_circ_164771,RMVar_hsa_circ_355791,RMVar_hsa_circ_164774 54254 RMVar_ID_54254 Human_SNP_ID_820167870 A-to-I Human chr13 + 19305041 19305041 19305041 TTTGGCTGTGACATCCACATACTGTCCTGGACAAAAGTGAGCAGCATAAAGAGGAGTGCCTGGTT TTTGGCTGTGACATCCACATACTGTCCTGGACGAAAGTGAGCAGCATAAAGAGGAGTGCCTGGTT A G - - Other Unknown GSE100210 HepG2 cell line chr13:19305040..19305041 29129909 RNA-Seq:(High) rs879057387 Functional Loss SNV ICGC 33..33 33 LAML 1 - 54255 RMVar_ID_54255 Human_SNP_ID_820186232 A-to-I Human chr13 - 21374437 21374437 21374437 TGAGGTCAGGGGTTCGAGATTAGCCTGGTCAAAATGGCAAAACCCTGTCTCCACTAAAAATACAA TGAGGTCAGGGGTTCGAGATTAGCCTGGTCAAGATGGCAAAACCCTGTCTCCACTAAAAATACAA T C ZDHHC20 Ensembl:ENSG00000180776 Protein coding 3'UTR GSE47997;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line chr13:21374436..21374437 23474544,31158229,31158229 RNA-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_26424827 RMVar_hsa_circ_82999,RMVar_hsa_circ_104322,RMVar_hsa_circ_112681,RMVar_hsa_circ_88460,RMVar_hsa_circ_162151,RMVar_hsa_circ_162153,RMVar_hsa_circ_162154,RMVar_hsa_circ_162152 54256 RMVar_ID_54256 Human_SNP_ID_820229903 A-to-I Human chr13 - 102181869 102181869 102181869 TTGTTCTTTCTTCCACAGATGCAGTTGGCAGAATAATGGTCTCCAAAGACGTCCATGCCGTAATC TTGTTCTTTCTTCCACAGATGCAGTTGGCAGAGTAATGGTCTCCAAAGACGTCCATGCCGTAATC T C FGF14 Ensembl:ENSG00000102466 Protein coding intron GSE107867 ASD brains,temporal_cortex chr13:102181868..102181869 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_280140 54257 RMVar_ID_54257 Human_SNP_ID_820234780 A-to-I Human chr13 - 98547426 98547426 98547426 CTCACGCCACAGCCTCCCGAGTAGCTGGGACTATAGGCGTGTGCCACCGTGCCCGGCTCATTGTT CTCACGCCACAGCCTCCCGAGTAGCTGGGACTGTAGGCGTGTGCCACCGTGCCCGGCTCATTGTT T C STK24 Ensembl:ENSG00000102572 Protein coding intron GSE100210 HepG2 cell line chr13:98547425..98547426 29129909 RNA-Seq:(High) rs369608682 Functional Loss SNV ICGC 33..33 33 LICA 1 - 54258 RMVar_ID_54258 Human_SNP_ID_820384490 A-to-I Human chr13 - 102134966 102134966 102134966 TTACCCAGACTGGTCTTGAACTCCTAGACTCAAGCAATCCCTCTACTTCGGCCTCCCAGATTGCT TTACCCAGACTGGTCTTGAACTCCTAGACTCATGCAATCCCTCTACTTCGGCCTCCCAGATTGCT T A FGF14 Ensembl:ENSG00000102466 Protein coding intron GSE107867 ASD brains,cerebellum;ASD brains,temporal_cortex chr13:102134965..102134966 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_23583610 RMVar_hsa_circ_280140 54259 RMVar_ID_54259 Human_SNP_ID_820391905 A-to-I Human chr13 - 102256429 102256429 102256429 CAGTGGCGTGATCACAGCTCACTGCAACTTCGACCTCCCGGGCTCAAGTGATCTTCCCACCTCAC CAGTGGCGTGATCACAGCTCACTGCAACTTCGGCCTCCCGGGCTCAAGTGATCTTCCCACCTCAC T C FGF14 Ensembl:ENSG00000102466 Protein coding intron GSE107867 ASD brains,frontal_cortex chr13:102256428..102256429 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 54260 RMVar_ID_54260 Human_SNP_ID_820394163 A-to-I Human chr13 - 67154429 67154429 67154429 GGGACTATAGGCACTTACCGCCGTGCCCAGCTAATTTTTGTATTTTCATAGAGACGAGGTTTTGC GGGACTATAGGCACTTACCGCCGTGCCCAGCTTATTTTTGTATTTTCATAGAGACGAGGTTTTGC T A PCDH9 Ensembl:ENSG00000184226 Protein coding intron GSE107867 ASD brains,frontal_cortex chr13:67154428..67154429 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 54261 RMVar_ID_54261 Human_SNP_ID_820478551 A-to-I Human chr13 + 52629840 52629840 52629840 GGCTGGGCATGGTGGCTCACGCCTGTAATCCCAGCAATTTAGAGGGCCGAGGCAGGCGGATCACG GGCTGGGCATGGTGGCTCACGCCTGTAATCCCTGCAATTTAGAGGGCCGAGGCAGGCGGATCACG A T MRPS31P4,AL137058.2 Ensembl:ENSG00000250299,Ensembl:ENSG00000273784 Pseudogene,lincRNA intron,intron GSE38233 cultured B-cells chr13:52629839..52629840 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - RMVar_hsa_circ_16683,RMVar_hsa_circ_296738,RMVar_hsa_circ_163563,RMVar_hsa_circ_27734,RMVar_hsa_circ_122428,RMVar_hsa_circ_163564,RMVar_hsa_circ_163562,RMVar_hsa_circ_357936,RMVar_hsa_circ_345949,RMVar_hsa_circ_345086 54262 RMVar_ID_54262 Human_SNP_ID_820512671 A-to-I Human chr13 - 77255175 77255175 77255175 GCAACTATGGAAAACATAGATTTTTCATTCGTATGAAGGTGACTCAAAAAACTGAAAATGGAGCT GCAACTATGGAAAACATAGATTTTTCATTCGTGTGAAGGTGACTCAAAAAACTGAAAATGGAGCT T C MYCBP2 Ensembl:ENSG00000005810 Protein coding intron GSE38233 cultured B-cells chr13:77255174..77255175 24183664 RNA-Seq:(High) rs948263437 Functional Loss SNV ICGC 33..33 33 LUSC 1 - RMVar_hsa_circ_79007,RMVar_hsa_circ_122811,RMVar_hsa_circ_163820,RMVar_hsa_circ_163821,RMVar_hsa_circ_3612,RMVar_hsa_circ_109703,RMVar_hsa_circ_163845,RMVar_hsa_circ_100693,RMVar_hsa_circ_163851,RMVar_hsa_circ_113731,RMVar_hsa_circ_103365,RMVar_hsa_circ_92922,RMVar_hsa_circ_163857,RMVar_hsa_circ_163859,RMVar_hsa_circ_163858,RMVar_hsa_circ_82867,RMVar_hsa_circ_163871,RMVar_hsa_circ_3929,RMVar_hsa_circ_98933,RMVar_hsa_circ_163889,RMVar_hsa_circ_34792,RMVar_hsa_circ_319130,RMVar_hsa_circ_45187,RMVar_hsa_circ_163897,RMVar_hsa_circ_110510,RMVar_hsa_circ_325966,RMVar_hsa_circ_268533,RMVar_hsa_circ_9368,RMVar_hsa_circ_163908,RMVar_hsa_circ_334568,RMVar_hsa_circ_372437,RMVar_hsa_circ_54481,RMVar_hsa_circ_163909,RMVar_hsa_circ_163910,RMVar_hsa_circ_102095,RMVar_hsa_circ_106883,RMVar_hsa_circ_106679,RMVar_hsa_circ_163916,RMVar_hsa_circ_163917,RMVar_hsa_circ_163915,RMVar_hsa_circ_271716,RMVar_hsa_circ_280227,RMVar_hsa_circ_319100,RMVar_hsa_circ_72890,RMVar_hsa_circ_163920,RMVar_hsa_circ_163922,RMVar_hsa_circ_54122,RMVar_hsa_circ_163921,RMVar_hsa_circ_163923,RMVar_hsa_circ_38542,RMVar_hsa_circ_323919,RMVar_hsa_circ_341923,RMVar_hsa_circ_55439,RMVar_hsa_circ_163924 54263 RMVar_ID_54263 Human_SNP_ID_820584218 A-to-I Human chr13 - 49668392 49668392 49668392 TTTTTTTGTATTTTTAGTAGAGACGGGGTTTCACCATGTTAGCCAGGATGGTCTCGATCTCCTGA TTTTTTTGTATTTTTAGTAGAGACGGGGTTTCGCCATGTTAGCCAGGATGGTCTCGATCTCCTGA T C EBPL Ensembl:ENSG00000123179 Protein coding intron GSE47997 K562 cells&HepG2 cells chr13:49668391..49668392 23474544 RNA-Seq:(High) rs184666784 Functional Loss SNV ICGC 33..33 33 COCA 1 - Human_RBP_ID_118729 54264 RMVar_ID_54264 Human_SNP_ID_820591146 A-to-I Human chr13 - 21374363 21374363 21374363 AAAACTGTCCAGGCATGGTGGCACACGCCTGTAGTCCCAACTACTCGGGAGGTGGAGGCAGGAGA AAAACTGTCCAGGCATGGTGGCACACGCCTGTGGTCCCAACTACTCGGGAGGTGGAGGCAGGAGA T C ZDHHC20 Ensembl:ENSG00000180776 Protein coding 3'UTR GSE47997;GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835;GSE123020:GSM3490829,GSM3490830,GSM3490831 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line;esophageal squamous carcinoma cells,EC109 cell line chr13:21374362..21374363 23474544,24183664,29129909,31158229,31158229,31158229,32596459 RNA-Seq:(High) rs748880972 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 haematopoietic and lymphoid tissue Human_RBP_ID_118323,Human_RBP_ID_17359167,Human_RBP_ID_23159647,Human_RBP_ID_23306400,Human_RBP_ID_26424826 RMVar_hsa_circ_82999,RMVar_hsa_circ_104322,RMVar_hsa_circ_112681,RMVar_hsa_circ_88460,RMVar_hsa_circ_162151,RMVar_hsa_circ_162153,RMVar_hsa_circ_162154,RMVar_hsa_circ_162152 54265 RMVar_ID_54265 Human_SNP_ID_820695542 A-to-I Human chr13 - 102139212 102139212 102139212 TTTCTATTTCATAGATGAGAAAACTGAGACTCAGATGAGTTATGAGCTTTCAAACTCTTCCGAGC TTTCTATTTCATAGATGAGAAAACTGAGACTCCGATGAGTTATGAGCTTTCAAACTCTTCCGAGC T G FGF14 Ensembl:ENSG00000102466 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank;ASD brains,frontal_cortex chr13:102139211..102139212 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_280140 54266 RMVar_ID_54266 Human_SNP_ID_820809585 A-to-I Human chr13 - 107856157 107856157 107856157 CATGCCTGTAATCCCAGCACTTTGGGAGGCTAAGACAGGAGGATCGCTTGAGTTCAGGAGTTTGA CATGCCTGTAATCCCAGCACTTTGGGAGGCTACGACAGGAGGATCGCTTGAGTTCAGGAGTTTGA T G FAM155A Ensembl:ENSG00000204442 Protein coding intron GSE107867 ASD brains,cerebellum chr13:107856156..107856157 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 54267 RMVar_ID_54267 Human_SNP_ID_820833368 A-to-I Human chr13 + 52030849 52030849 52030849 GCGCAACATCCACGCAGCAGCTCATCAGGTACAAGTGCTTCCATATCCATTTACCCACCATCGGC GCGCAACATCCACGCAGCAGCTCATCAGGTACGAGTGCTTCCATATCCATTTACCCACCATCGGC A G ALG11,UTP14C Ensembl:ENSG00000253710,Ensembl:ENSG00000253797 Protein coding,Protein coding 3'UTR,CDS GSE100210;GSE107867 HepG2 cell line;ASD brains,frontal_cortex chr13:52030848..52030849 29129909,30559470 RNA-Seq:(High) rs772344954 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue Human_RBP_ID_3433066,Human_RBP_ID_17245141,Human_RBP_ID_17360102 54268 RMVar_ID_54268 Human_SNP_ID_880050994 A-to-I Human chrX - 75742456 75742456 75742456 AAGTCAATACTGAGCCATATAATCCTTTTGAGAAACAACAAGGGGAAATTTCACGGATTGAAAAG AAGTCAATACTGAGCCATATAATCCTTTTGAGGAACAACAAGGGGAAATTTCACGGATTGAAAAG T C TTC3P1 Ensembl:ENSG00000215105 Pseudogene exon GSE100210 HepG2 cell line chrX:75742455..75742456 29129909 RNA-Seq:(High) rs879057871 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_3932049 54269 RMVar_ID_54269 Human_SNP_ID_880075000 A-to-I Human chrX - 140723963 140723963 140723963 GTGTATGGAATGTGTGTGTGTATGGAATGGGTAACTGTGCATGTGTATGGAATGTGTGTGTATGG GTGTATGGAATGTGTGTGTGTATGGAATGGGTGACTGTGCATGTGTATGGAATGTGTGTGTATGG T C lnc-CDR1-1,lnc-CDR1-1:2,lnc-CDR1-3 RNACentral:URS00008B1FC3,RNACentral:URS00008BCC8C,RNACentral:URS00008B60B1 lincRNA,lincRNA,lincRNA intron,intron,intron GSE107867 ASD brains,cerebellum chrX:140723962..140723963 30559470 RNA-Seq:(High) rs889086177 Functional Loss SNV ICGC 33..33 33 CHOL 1 - 54270 RMVar_ID_54270 Human_SNP_ID_880117879 A-to-I Human chrX - 152189847 152189847 152189847 GTGGCATATGCGACGGCCATGGACTGGTTCATAGCCGTCTGTTATGCCTTTGTATTTTCTGCACT GTGGCATATGCGACGGCCATGGACTGGTTCATGGCCGTCTGTTATGCCTTTGTATTTTCTGCACT T C GABRA3 Ensembl:ENSG00000011677 Protein coding CDS GSE56152 embryonic stem cells,wild type chrX:152189846..152189847 25708366 RNA-Seq:(High) rs2229939 Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_Splice_Rec_2242985,Human_Splice_Rec_2243003 RMVar_hsa_circ_264159,RMVar_hsa_circ_122101,RMVar_hsa_circ_108814,RMVar_hsa_circ_264161,RMVar_hsa_circ_315202,RMVar_hsa_circ_264158,RMVar_hsa_circ_310857,RMVar_hsa_circ_264160 54271 RMVar_ID_54271 Human_SNP_ID_880207780 A-to-I Human chrX + 123913039 123913039 123913039 CTGATCTCAGGTGATCTGCCTGCCTCGGCCTCACAAAGTGCTGGGATTACAGGTGTGAACCACTG CTGATCTCAGGTGATCTGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAACCACTG A C XIAP Ensembl:ENSG00000101966 Protein coding 3'UTR GSE38233;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,KYSE180 cell line chrX:123913038..123913039 24183664,32596459 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_5050994 RMVar_hsa_circ_98508,RMVar_hsa_circ_263727 54272 RMVar_ID_54272 Human_SNP_ID_880318383 A-to-I Human chrX + 75584103 75584103 75584103 GAAGTCATCTTCATCCTCAGAAGACAGGAATCAAATGAAAACACTTGGTAGACAGGACTTGAATG GAAGTCATCTTCATCCTCAGAAGACAGGAATCGAATGAAAACACTTGGTAGACAGGACTTGAATG A G BRAFP1 Ensembl:ENSG00000224775 Pseudogene exon GSE100210 HepG2 cell line chrX:75584102..75584103 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 1 - RMVar_hsa_circ_263073 54273 RMVar_ID_54273 Human_SNP_ID_880356972 A-to-I Human chrX + 15741248 15741248 15741248 CACCACCATGCACGGCTAATTTTTGTACTTTTAGTGGAGATGGGGTTTTGCTATGTTGGCCAGGC CACCACCATGCACGGCTAATTTTTGTACTTTTGGTGGAGATGGGGTTTTGCTATGTTGGCCAGGC A G CA5B Ensembl:ENSG00000169239 Protein coding intron GSE100210 HepG2 cell line chrX:15741247..15741248 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_48975,RMVar_hsa_circ_261416,RMVar_hsa_circ_86073,RMVar_hsa_circ_95743,RMVar_hsa_circ_261415,RMVar_hsa_circ_261417 54274 RMVar_ID_54274 Human_SNP_ID_880391055 A-to-I Human chrX - 74209011 74209010 74209011 CAAAACCTAGGCAGCCTGGCCAACATGGTGAAACCCCATCTTCACAAAAAATTATGACAATTTGC CAAAACCTAGGCAGCCTGGCCAACATGGTGAA_CCCCATCTTCACAAAAAATTATGACAATTTGC GT G FTX Ensembl:ENSG00000230590 lincRNA intron GSE100210 HepG2 cell line chrX:74209010..74209011 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 33..33 33 BRCA 1 - Human_RBP_ID_3264653,Human_RBP_ID_3931802,Human_RBP_ID_9248964,Human_RBP_ID_16935866,Human_RBP_ID_26745959 54275 RMVar_ID_54275 Human_SNP_ID_880428667 A-to-I Human chrX + 121049252 121049252 121049252 CACAATGGAGCGTTCTGCCAGGCAAATTATGCACACAGCCATGAAGTATAACCTGGGATTGGACC CACAATGGAGCGTTCTGCCAGGCAAATTATGCGCACAGCCATGAAGTATAACCTGGGATTGGACC A G GLUD2 Ensembl:ENSG00000182890 Protein coding CDS GSE100210 HepG2 cell line chrX:121049251..121049252 29129909 RNA-Seq:(High) rs778620218 Functional Loss SNV ICGC 33..33 33 PRAD 1 - 54276 RMVar_ID_54276 Human_SNP_ID_880449656 A-to-I Human chrX - 39788157 39788157 39788157 AGTCAGCCGCATCTTCTTTTGCATCGTCAGCCAAACCACATCCCTGAGACACCATGGGGAAGGTG AGTCAGCCGCATCTTCTTTTGCATCGTCAGCCGAACCACATCCCTGAGACACCATGGGGAAGGTG T C - - Other Unknown GSE100210 HepG2 cell line chrX:39788156..39788157 29129909 RNA-Seq:(High) rs763992138 Functional Loss SNV ICGC 33..33 33 PAAD 1 - 54277 RMVar_ID_54277 Human_SNP_ID_880490401 A-to-I Human chrX - 152828571 152828571 152828571 TTCGTTCAAAAATCTGAAACGCGTGGCCAAGGAGTTGGGTGAGAACCTGACTGATGAGGAGCTGC TTCGTTCAAAAATCTGAAACGCGTGGCCAAGGTGTTGGGTGAGAACCTGACTGATGAGGAGCTGC T A CETN2 Ensembl:ENSG00000147400 Protein coding CDS GSE100210 HepG2 cell line chrX:152828570..152828571 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA 33..33 33 OV 1 - Human_RBP_ID_968728,Human_RBP_ID_5055675,Human_RBP_ID_9409556,Human_RBP_ID_24334218 Human_Splice_Rec_2243276,Human_Splice_Rec_2243279 RMVar_hsa_circ_264170,RMVar_hsa_circ_118681,RMVar_hsa_circ_120465,RMVar_hsa_circ_90359,RMVar_hsa_circ_264171,RMVar_hsa_circ_264169 54278 RMVar_ID_54278 Human_SNP_ID_880512635 A-to-I Human chrX + 57394177 57394177 57394177 GGAATGACCTGGGAGTAGCCGCCTCCTGCAACACCACCTTTTATTCCAAAGGTGGGGCCCTGAGA GGAATGACCTGGGAGTAGCCGCCTCCTGCAACGCCACCTTTTATTCCAAAGGTGGGGCCCTGAGA A G FAAH2 Ensembl:ENSG00000165591 Protein coding intron GSE100210 HepG2 cell line chrX:57394176..57394177 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 1 - RMVar_hsa_circ_6235,RMVar_hsa_circ_262687 54279 RMVar_ID_54279 Human_SNP_ID_880534723 A-to-I Human chrX - 150231505 150231505 150231505 CTCCAGAGCAGGTGGACAAGATGAAGGCTATCATTGAGAAGCTTCGCTTCACGTACAGAAGTGAC CTCCAGAGCAGGTGGACAAGATGAAGGCTATCGTTGAGAAGCTTCGCTTCACGTACAGAAGTGAC T C XRCC6P2 Ensembl:ENSG00000234825 Pseudogene exon GSE100210 HepG2 cell line chrX:150231504..150231505 29129909 RNA-Seq:(High) rs782095608 Functional Loss SNV ICGC 33..33 33 LAML 1 - 54280 RMVar_ID_54280 Human_SNP_ID_880585277 A-to-I Human chrX + 103651907 103651907 103651907 ATTAGAGTGATATAGCTAATGGTAAAAAATGGATGATTCCATAATGATGTGAAGAAGGACACCTT ATTAGAGTGATATAGCTAATGGTAAAAAATGGGTGATTCCATAATGATGTGAAGAAGGACACCTT A G - - Other Unknown GSE100210 HepG2 cell line chrX:103651906..103651907 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 2 - 54281 RMVar_ID_54281 Human_SNP_ID_880628572 A-to-I Human chrX - 77827319 77827319 77827319 CTGTTCTATGTTTTGCTGTTATTTTAGTCTTTATTCTCTTCCTTTAGGTGGAGAAACAAAGTACC CTGTTCTATGTTTTGCTGTTATTTTAGTCTTTGTTCTCTTCCTTTAGGTGGAGAAACAAAGTACC T C MAGT1 Ensembl:ENSG00000102158 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector chrX:77827318..77827319 29967493 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_739707,Human_RBP_ID_1343664,Human_RBP_ID_1406737,Human_RBP_ID_3929331,Human_RBP_ID_8026594,Human_RBP_ID_17555830,Human_RBP_ID_24354630,Human_RBP_ID_24445119,Human_RBP_ID_26297558,Human_RBP_ID_27796168 Human_miRNA_ID_299574,Human_miRNA_ID_1755068 RMVar_hsa_circ_91900,RMVar_hsa_circ_124274,RMVar_hsa_circ_117232,RMVar_hsa_circ_263096,RMVar_hsa_circ_263098,RMVar_hsa_circ_81524,RMVar_hsa_circ_263097,RMVar_hsa_circ_263095 54282 RMVar_ID_54282 Human_SNP_ID_880632757 A-to-I Human chrX + 75584124 75584124 75584124 AGACAGGAATCAAATGAAAACACTTGGTAGACAGGACTTGAATGATGATTGGGAGATTCCTGATG AGACAGGAATCAAATGAAAACACTTGGTAGACGGGACTTGAATGATGATTGGGAGATTCCTGATG A G BRAFP1 Ensembl:ENSG00000224775 Pseudogene exon GSE100210 HepG2 cell line chrX:75584123..75584124 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 2 - RMVar_hsa_circ_263073 54283 RMVar_ID_54283 Human_SNP_ID_880667277 A-to-I Human chrX - 101050876 101050876 101050876 CACCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGACTGGGTTTCACTCTGTTGGTCAGGCTGC CACCACGCCCAGCTAATTTTTGTATTTTTAGTGGAGACTGGGTTTCACTCTGTTGGTCAGGCTGC T C TRMT2B,TRMT2B-AS1 Ensembl:ENSG00000188917,Ensembl:ENSG00000225839 Protein coding,lincRNA intron,intron GSE100210 HepG2 cell line chrX:101050875..101050876 29129909 RNA-Seq:(High) rs1345418108 Functional Loss SNV ICGC 33..33 33 PRAD 1 - Human_RBP_ID_16772712 RMVar_hsa_circ_120367,RMVar_hsa_circ_263275,RMVar_hsa_circ_266294,RMVar_hsa_circ_266193 54284 RMVar_ID_54284 Human_SNP_ID_880668969 A-to-I Human chrX - 2261432 2261432 2261432 ATAAGCAGATCACATCCAGAACAACCCCACCCAACAGAAATGACAGCTACTTCCTAGAGACTTTA ATAAGCAGATCACATCCAGAACAACCCCACCCGACAGAAATGACAGCTACTTCCTAGAGACTTTA T C DHRSX Ensembl:ENSG00000169084 Protein coding intron GSE38233 cultured B-cells chrX:2261431..2261432 24183664 RNA-Seq:(High) rs35731332 Functional Loss SNV ICGC 33..33 33 SKCA 1 - RMVar_hsa_circ_261193,RMVar_hsa_circ_318035,RMVar_hsa_circ_341978,RMVar_hsa_circ_82687,RMVar_hsa_circ_261191,RMVar_hsa_circ_261192 54285 RMVar_ID_54285 Human_SNP_ID_880679091 A-to-I Human chrX - 53664325 53664325 53664325 TTTTAGGCCTGGCACAGTGGCTAACGCCTGTAATCTCAGCACTTTGGGAGGCTGAGGCCAGGAGG TTTTAGGCCTGGCACAGTGGCTAACGCCTGTAGTCTCAGCACTTTGGGAGGCTGAGGCCAGGAGG T C HUWE1 Ensembl:ENSG00000086758 Protein coding intron GSE100210 HepG2 cell line chrX:53664324..53664325 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_49196,RMVar_hsa_circ_40553,RMVar_hsa_circ_369246,RMVar_hsa_circ_22480,RMVar_hsa_circ_60780,RMVar_hsa_circ_31367,RMVar_hsa_circ_344757,RMVar_hsa_circ_275568,RMVar_hsa_circ_335287,RMVar_hsa_circ_62041 54286 RMVar_ID_54286 Human_SNP_ID_880737609 A-to-I Human chrX - 101010396 101010396 101010396 TGAGGCAGATTTTTTTTTTGAGATAGAGTCTCACTCTTGCCCAGGCTGGAGTGTCGTGGCGTGAT TGAGGCAGATTTTTTTTTTGAGATAGAGTCTCTCTCTTGCCCAGGCTGGAGTGTCGTGGCGTGAT T A TRMT2B Ensembl:ENSG00000188917 Protein coding 3'UTR GSE100210 HepG2 cell line chrX:101010395..101010396 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_18142503 54287 RMVar_ID_54287 Human_SNP_ID_880758904 A-to-I Human chrX + 71420259 71420259 71420259 ATCTGTTGTGCTGATTCCTGGTCTGTTGGTTCATTTTGGGATCACCTTGATTTGCCTTCCTCTAA ATCTGTTGTGCTGATTCCTGGTCTGTTGGTTCGTTTTGGGATCACCTTGATTTGCCTTCCTCTAA A G TAF1 Ensembl:ENSG00000147133 Protein coding intron GSE100210 HepG2 cell line chrX:71420258..71420259 29129909 RNA-Seq:(High) rs879039537 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_16921660 RMVar_hsa_circ_64295,RMVar_hsa_circ_355603,RMVar_hsa_circ_329396,RMVar_hsa_circ_302512,RMVar_hsa_circ_75437,RMVar_hsa_circ_104665,RMVar_hsa_circ_262929,RMVar_hsa_circ_262930,RMVar_hsa_circ_62329,RMVar_hsa_circ_374581,RMVar_hsa_circ_337595,RMVar_hsa_circ_295602,RMVar_hsa_circ_262935,RMVar_hsa_circ_29000,RMVar_hsa_circ_21188,RMVar_hsa_circ_90821,RMVar_hsa_circ_262938,RMVar_hsa_circ_67237,RMVar_hsa_circ_282933,RMVar_hsa_circ_32131,RMVar_hsa_circ_36045,RMVar_hsa_circ_5407,RMVar_hsa_circ_8206,RMVar_hsa_circ_14702 54288 RMVar_ID_54288 Human_SNP_ID_880797476 A-to-I Human chrX - 46419302 46419302 46419302 CTTTTGATGCCAACAAACTGTATTGCAGTGAAATGCAGGCCATATTGCTCCAGGACAATGATGAA CTTTTGATGCCAACAAACTGTATTGCAGTGAAGTGCAGGCCATATTGCTCCAGGACAATGATGAA T C AL139811.2 Ensembl:ENSG00000231235 Pseudogene exon GSE100210 HepG2 cell line chrX:46419301..46419302 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 1 - 54289 RMVar_ID_54289 Human_SNP_ID_880804067 A-to-I Human chrX + 130496267 130496267 130496267 GTGTGACAGAACGTATCACTGATGACTGATAGAAAGCCCTCTTTCACTCTGATTACCCACTCACT GTGTGACAGAACGTATCACTGATGACTGATAGTAAGCCCTCTTTCACTCTGATTACCCACTCACT A T DENND10P1 Ensembl:ENSG00000221930 Pseudogene exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chrX:130496266..130496267 30559470 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - RMVar_hsa_circ_268525 54290 RMVar_ID_54290 Human_SNP_ID_880811790 A-to-I Human chrX - 153032668 153032668 153032668 TCCGGGTATGGTGGTTGCACGCCTGTGGTCCCAGCTAGTCGGGAGGCTGAGGCGGGAGAATCGCT TCCGGGTATGGTGGTTGCACGCCTGTGGTCCCGGCTAGTCGGGAGGCTGAGGCGGGAGAATCGCT T C lnc-PNMA5-2 RNACentral:URS00008C090D lincRNA intron GSE100210 HepG2 cell line chrX:153032667..153032668 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ORCA 1 - 54291 RMVar_ID_54291 Human_SNP_ID_880851670 A-to-I Human chrX - 45848396 45848396 45848396 GCGATCTGCCTGCCCTGGCCTCCCACAGTGTTAGGACTACAGGCATGAGCCACTGCACCCAGCCA GCGATCTGCCTGCCCTGGCCTCCCACAGTGTTTGGACTACAGGCATGAGCCACTGCACCCAGCCA T A LINC02595 Ensembl:ENSG00000231566 lincRNA intron GSE100210 HepG2 cell line chrX:45848395..45848396 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_3257347,Human_RBP_ID_16894355,Human_RBP_ID_17580051,Human_RBP_ID_26797295 54292 RMVar_ID_54292 Human_SNP_ID_880873285 A-to-I Human chrX - 74583207 74583207 74583207 AGATTGATAATTCAGAACTTCTTCATATGCTCAAGTCTCCAGAGTCACTCCATTCTAAGGTTGAT AGATTGATAATTCAGAACTTCTTCATATGCTCGAGTCTCCAGAGTCACTCCATTCTAAGGTTGAT T C RLIM,PABPC1P3 Ensembl:ENSG00000131263,Ensembl:ENSG00000230673 Protein coding,Pseudogene 3'UTR,exon GSE100210 HepG2 cell line chrX:74583206..74583207 29129909 RNA-Seq:(High) rs879068026 Functional Loss SNV ICGC 33..33 33 COCA 1 - Human_miRNA_ID_1886799,Human_miRNA_ID_1887661 54293 RMVar_ID_54293 Human_SNP_ID_880913656 A-to-I Human chrX + 121048582 121048582 121048582 ACATGAGCATTTTAGGAATGACACCAGGGTTTAGAGATAAAACATTTGTTGTTCAGGGATTTGGT ACATGAGCATTTTAGGAATGACACCAGGGTTTGGAGATAAAACATTTGTTGTTCAGGGATTTGGT A G GLUD2 Ensembl:ENSG00000182890 Protein coding CDS GSE100210 HepG2 cell line chrX:121048581..121048582 29129909 RNA-Seq:(High) rs776965882 Functional Loss SNV ICGC 33..33 33 LAML 2 - 54294 RMVar_ID_54294 Human_SNP_ID_880955853 A-to-I Human chrX + 9546331 9546331 9546331 GTCAGGAGATCGAGACCCATCCTGGCTAACACAGTGAAACCCCATTTCTACTAAAAGTACAAAAA GTCAGGAGATCGAGACCCATCCTGGCTAACACGGTGAAACCCCATTTCTACTAAAAGTACAAAAA A G TBL1X Ensembl:ENSG00000101849 Protein coding intron GSE100210 HepG2 cell line chrX:9546330..9546331 29129909 RNA-Seq:(High) rs775424891 Functional Loss SNV ICGC 33..33 33 BOCA 1 - RMVar_hsa_circ_9222 54295 RMVar_ID_54295 Human_SNP_ID_881002114 A-to-I Human chrX + 124002172 124002172 124002172 CCAGGAATTTGAGGTTGCAGTGAACTGTGATCATGCCACTGCACTGTAGTCTGGGCGACAGAGGG CCAGGAATTTGAGGTTGCAGTGAACTGTGATCTTGCCACTGCACTGTAGTCTGGGCGACAGAGGG A T STAG2 Ensembl:ENSG00000101972 Protein coding intron GSE100210 HepG2 cell line chrX:124002171..124002172 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - Human_RBP_ID_8712512,Human_RBP_ID_16812972,Human_RBP_ID_26302925 RMVar_hsa_circ_263729,RMVar_hsa_circ_117204 54296 RMVar_ID_54296 Human_SNP_ID_881060637 A-to-I Human chrX + 73525322 73525322 73525322 TCAGAGCAGACATCATATGCTTGTCATGATGCACTTGGGTCTATTCTTTCAGGTGCCATGTATGG TCAGAGCAGACATCATATGCTTGTCATGATGCGCTTGGGTCTATTCTTTCAGGTGCCATGTATGG A G - - Other Unknown GSE100210 HepG2 cell line chrX:73525321..73525322 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 1 - 54297 RMVar_ID_54297 Human_SNP_ID_881070930 A-to-I Human chrX - 150232733 150232733 150232733 AAGGCTATGTTTGAATCTCCTAGTGAAGATGAATTGACACCTTTTGACATGAGCATCCAGTGTAT AAGGCTATGTTTGAATCTCCTAGTGAAGATGAGTTGACACCTTTTGACATGAGCATCCAGTGTAT T C XRCC6P2 Ensembl:ENSG00000234825 Pseudogene exon GSE100210 HepG2 cell line chrX:150232732..150232733 29129909 RNA-Seq:(High) rs781989912 Functional Loss SNV ICGC 33..33 33 LAML 2 - 54298 RMVar_ID_54298 Human_SNP_ID_881090250 A-to-I Human chrX - 68352902 68352902 68352902 GCAATCCACTCGCCTCAGCCTCCCATAGTGTTAGGATTACAGGCGTAAGCCACTGCACCGGGCCT GCAATCCACTCGCCTCAGCCTCCCATAGTGTTGGGATTACAGGCGTAAGCCACTGCACCGGGCCT T C OPHN1 Ensembl:ENSG00000079482 Protein coding intron GSE100210 HepG2 cell line chrX:68352901..68352902 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 CLLE 1 - 54299 RMVar_ID_54299 Human_SNP_ID_881107894 A-to-I Human chrX + 44030428 44030428 44030428 TCGTCTTCAGTTAGTGGCAAGACTTGCAGAGGATACAGGTTTGCAGATTCCACCAGCAGCACAGC TCGTCTTCAGTTAGTGGCAAGACTTGCAGAGGGTACAGGTTTGCAGATTCCACCAGCAGCACAGC A G AL034370.1 Ensembl:ENSG00000214019 Pseudogene exon GSE100210 HepG2 cell line chrX:44030427..44030428 29129909 RNA-Seq:(High) rs879037187 Functional Loss SNV ICGC 33..33 33 LAML 1 - 54300 RMVar_ID_54300 Human_SNP_ID_881229967 A-to-I Human chrX + 85091284 85091284 85091284 AAAATAAATAATAAAAAATAAAGGTATATAATATGTCTTAGATTTGATGAAATATGAGTGTGTTT AAAATAAATAATAAAAAATAAAGGTATATAATCTGTCTTAGATTTGATGAAATATGAGTGTGTTT A C APOOL Ensembl:ENSG00000155008 Protein coding 3'UTR GSE47997;GSE38233;GSE100210 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line chrX:85091283..85091284 23474544,24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 54301 RMVar_ID_54301 Human_SNP_ID_881258612 A-to-I Human chrX - 51744604 51744604 51744604 TTTGCCAACATCGCATGTTCTCTTGTCTGTCCACCTTTTTCAAATCCAGTTTCAAACTCTCCTTT TTTGCCAACATCGCATGTTCTCTTGTCTGTCCTCCTTTTTCAAATCCAGTTTCAAACTCTCCTTT T A lnc-CENPVL2-3 RNACentral:URS0000D59CA6 lincRNA intron GSE38233 cultured B-cells chrX:51744603..51744604 24183664 RNA-Seq:(High) rs879978767 Functional Loss SNV ICGC 33..33 33 LAML 1 - 54302 RMVar_ID_54302 Human_SNP_ID_881262343 A-to-I Human chrX - 85863096 85863094 85863097 AGAGCAAGACTCTGTCTCACAAAAAAAAAAAAAGGGGGCTGTACATAGGCAGCAAACTAAGCTGC AGAGCAAGACTCTGTCTCACAAAAAAAAAAA___GGGGCTGTACATAGGCAGCAAACTAAGCTGC CCTT C CHM Ensembl:ENSG00000188419 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line chrX:85863095..85863096 31158229 RNA-Seq:(High) - Functional Loss DEL TCGA 32..34 33 UCEC 1 - Human_RBP_ID_740400 Human_miRNA_ID_187909 54303 RMVar_ID_54303 Human_SNP_ID_881284590 A-to-I Human chrX + 75584926 75584926 75584926 GAGATGAGAGACCACTCTTTCCCCAAATTCTCACCTCTATTAAGCTGCTGACCCGCTCATTGCCA GAGATGAGAGACCACTCTTTCCCCAAATTCTCGCCTCTATTAAGCTGCTGACCCGCTCATTGCCA A G BRAFP1 Ensembl:ENSG00000224775 Pseudogene exon GSE100210 HepG2 cell line chrX:75584925..75584926 29129909 RNA-Seq:(High) rs1193016683 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_9250530 RMVar_hsa_circ_263073 54304 RMVar_ID_54304 Human_SNP_ID_881335959 A-to-I Human chrX + 57238282 57238282 57238282 TGTCCATCAATGGTAGAAAGGATGAAGAAAATATGTTAAATATACACCATGGAATACTATGCAGC TGTCCATCAATGGTAGAAAGGATGAAGAAAATTTGTTAAATATACACCATGGAATACTATGCAGC A T - - Other Unknown GSE100210 HepG2 cell line chrX:57238281..57238282 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - 54305 RMVar_ID_54305 Human_SNP_ID_881356483 A-to-I Human chrX - 72469322 72469322 72469322 AAATTAAAAATTAGCTGGATGTGGTGGCCTATAGTCCCAGCAACTTGGGAAGCTGAGGTGGGAGG AAATTAAAAATTAGCTGGATGTGGTGGCCTATGGTCCCAGCAACTTGGGAAGCTGAGGTGGGAGG T C HDAC8,AL133500.1 Ensembl:ENSG00000147099,Ensembl:ENSG00000285547 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line chrX:72469321..72469322 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - RMVar_hsa_circ_78337,RMVar_hsa_circ_92747,RMVar_hsa_circ_262992,RMVar_hsa_circ_108842,RMVar_hsa_circ_262996,RMVar_hsa_circ_273345,RMVar_hsa_circ_320195,RMVar_hsa_circ_262993,RMVar_hsa_circ_335486,RMVar_hsa_circ_262994,RMVar_hsa_circ_262995,RMVar_hsa_circ_81047,RMVar_hsa_circ_262998,RMVar_hsa_circ_262999 54306 RMVar_ID_54306 Human_SNP_ID_881422557 A-to-I Human chrX - 10972101 10972101 10972101 TTTGTTTTTGCTATTTTGATTTAAGATACATCAAAGCAAATTGGAATGTGGTTATAATGGAGCAA TTTGTTTTTGCTATTTTGATTTAAGATACATCGAAGCAAATTGGAATGTGGTTATAATGGAGCAA T C AC073529.1 Ensembl:ENSG00000234129 lincRNA intron GSE100210 HepG2 cell line chrX:10972100..10972101 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 54307 RMVar_ID_54307 Human_SNP_ID_881444995 A-to-I Human chrX - 77828212 77828212 77828212 CTATTGGGAGTCCGAGGCAGGTGGATTGCTTGAGGCCAGGAGTTAGAGACCAGCCTGGCCAACAA CTATTGGGAGTCCGAGGCAGGTGGATTGCTTGCGGCCAGGAGTTAGAGACCAGCCTGGCCAACAA T G MAGT1 Ensembl:ENSG00000102158 Protein coding 3'UTR GSE100210 HepG2 cell line chrX:77828211..77828212 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_739720,Human_RBP_ID_23204796 Human_miRNA_ID_274336 RMVar_hsa_circ_91900,RMVar_hsa_circ_124274,RMVar_hsa_circ_117232,RMVar_hsa_circ_263096,RMVar_hsa_circ_263098,RMVar_hsa_circ_81524,RMVar_hsa_circ_263097,RMVar_hsa_circ_263095 54308 RMVar_ID_54308 Human_SNP_ID_881457972 A-to-I Human chrX - 73223244 73223244 73223244 TCTCTCCTTGGCAAGCTTCTGTTTCTTTCTTCATTCTCGAAGCCTGTTCTTGAAGTTGGGGTCAC TCTCTCCTTGGCAAGCTTCTGTTTCTTTCTTCGTTCTCGAAGCCTGTTCTTGAAGTTGGGGTCAC T C - - Other Unknown GSE100210 HepG2 cell line chrX:73223243..73223244 29129909 RNA-Seq:(High) rs879047307 Functional Loss SNV ICGC 33..33 33 LAML 1 - 54309 RMVar_ID_54309 Human_SNP_ID_881481324 A-to-I Human chrX - 39788155 39788155 39788155 TCAGCCGCATCTTCTTTTGCATCGTCAGCCAAACCACATCCCTGAGACACCATGGGGAAGGTGAA TCAGCCGCATCTTCTTTTGCATCGTCAGCCAAGCCACATCCCTGAGACACCATGGGGAAGGTGAA T C - - Other Unknown GSE100210 HepG2 cell line chrX:39788154..39788155 29129909 RNA-Seq:(High) rs760512065 Functional Loss SNV ICGC 33..33 33 PAAD 1 - 54310 RMVar_ID_54310 Human_SNP_ID_881483349 A-to-I Human chrX - 93222528 93222528 93222528 TGTGCTTTTTGTAGAAGACAGCAAAATGGAGCACCAGGTCGTCCTTGCAACATGGAAGAATATTC TGTGCTTTTTGTAGAAGACAGCAAAATGGAGCGCCAGGTCGTCCTTGCAACATGGAAGAATATTC T C AL359263.1 Ensembl:ENSG00000234130 Pseudogene exon GSE100210 HepG2 cell line chrX:93222527..93222528 29129909 RNA-Seq:(High) rs1263098935 Functional Loss SNV ICGC 33..33 33 LAML 2 - 54311 RMVar_ID_54311 Human_SNP_ID_881494197 A-to-I Human chrX - 129489032 129489032 129489032 CTAACAAGCTGGCAAAAGAGGAAATGTTACAAATGATACGGCATGGAGCCACCCATGTTTTTGCT CTAACAAGCTGGCAAAAGAGGAAATGTTACAAGTGATACGGCATGGAGCCACCCATGTTTTTGCT T C SMARCA1 Ensembl:ENSG00000102038 Protein coding exon GSE100210 HepG2 cell line chrX:129489031..129489032 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC 33..33 33 LIHC 2 - Human_RBP_ID_24328091,Human_RBP_ID_27143470 Human_Splice_Rec_2234403,Human_Splice_Rec_2234404,Human_Splice_Rec_2234447,Human_Splice_Rec_2234448,Human_Splice_Rec_2234493,Human_Splice_Rec_2234494,Human_Splice_Rec_2234541,Human_Splice_Rec_2234542 RMVar_hsa_circ_64878,RMVar_hsa_circ_337875,RMVar_hsa_circ_62666,RMVar_hsa_circ_368698,RMVar_hsa_circ_57048,RMVar_hsa_circ_15402,RMVar_hsa_circ_48670,RMVar_hsa_circ_285044,RMVar_hsa_circ_28016,RMVar_hsa_circ_67349,RMVar_hsa_circ_263799,RMVar_hsa_circ_360868,RMVar_hsa_circ_48126,RMVar_hsa_circ_305421,RMVar_hsa_circ_263800,RMVar_hsa_circ_331995,RMVar_hsa_circ_360954,RMVar_hsa_circ_368485,RMVar_hsa_circ_299513,RMVar_hsa_circ_8333,RMVar_hsa_circ_11534,RMVar_hsa_circ_66097,RMVar_hsa_circ_8832,RMVar_hsa_circ_50863,RMVar_hsa_circ_263802,RMVar_hsa_circ_263803,RMVar_hsa_circ_263801,RMVar_hsa_circ_316204,RMVar_hsa_circ_350115,RMVar_hsa_circ_361398,RMVar_hsa_circ_326598,RMVar_hsa_circ_64464,RMVar_hsa_circ_59938,RMVar_hsa_circ_263805,RMVar_hsa_circ_324249,RMVar_hsa_circ_263804,RMVar_hsa_circ_271430,RMVar_hsa_circ_263806 54312 RMVar_ID_54312 Human_SNP_ID_881514856 A-to-I Human chrX - 93223587 93223587 93223587 AGAAAGCTTCCTGGAGGGTTTTCATGATGAAAACACCCAGGTGCAGCTCACTCTGCTTACTGCCA AGAAAGCTTCCTGGAGGGTTTTCATGATGAAAGCACCCAGGTGCAGCTCACTCTGCTTACTGCCA T C AL359263.1 Ensembl:ENSG00000234130 Pseudogene exon GSE100210 HepG2 cell line chrX:93223586..93223587 29129909 RNA-Seq:(High) rs1157690462 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_17328526 54313 RMVar_ID_54313 Human_SNP_ID_881584233 A-to-I Human chrX + 57393640 57393640 57393640 ACTATCAATGCACCACTCACCCCCAGATCTTCAGCACTGACGGGGTCTCCTTTCTTACTGGATGC ACTATCAATGCACCACTCACCCCCAGATCTTCGGCACTGACGGGGTCTCCTTTCTTACTGGATGC A G FAAH2 Ensembl:ENSG00000165591 Protein coding intron GSE100210 HepG2 cell line chrX:57393639..57393640 29129909 RNA-Seq:(High) rs1263497523 Functional Loss SNV ICGC 33..33 33 LAML 2 - RMVar_hsa_circ_6235,RMVar_hsa_circ_262686,RMVar_hsa_circ_262687 54314 RMVar_ID_54314 Human_SNP_ID_881609953 A-to-I Human chrX + 73525297 73525297 73525297 CAATGTGATCCCCAAACTCCAGACATCAGAGCAGACATCATATGCTTGTCATGATGCACTTGGGT CAATGTGATCCCCAAACTCCAGACATCAGAGCGGACATCATATGCTTGTCATGATGCACTTGGGT A G - - Other Unknown GSE100210 HepG2 cell line chrX:73525296..73525297 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 1 - 54315 RMVar_ID_54315 Human_SNP_ID_881640004 A-to-I Human chrX - 150232154 150232154 150232154 CTAGAAGACCTGTTGCAGAAGGTTCACGCCAAAGAGACCAGGAAGCGAGCACTCAGCAGGTTAAA CTAGAAGACCTGTTGCAGAAGGTTCACGCCAAGGAGACCAGGAAGCGAGCACTCAGCAGGTTAAA T C XRCC6P2 Ensembl:ENSG00000234825 Pseudogene exon GSE100210 HepG2 cell line chrX:150232153..150232154 29129909 RNA-Seq:(High) rs782692975 Functional Loss SNV ICGC 33..33 33 LAML 2 - 54316 RMVar_ID_54316 Human_SNP_ID_881871776 A-to-I Human chrX - 54072986 54072986 54072986 CTTCACCAAACCAGGAAGAGGGAAAAACTTTTACTTTTCTGATTTTAGGCCCAAGCTAGAGGAGG CTTCACCAAACCAGGAAGAGGGAAAAACTTTTGCTTTTCTGATTTTAGGCCCAAGCTAGAGGAGG T C FAM120C Ensembl:ENSG00000184083 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line chrX:54072985..54072986 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_8010687 RMVar_hsa_circ_265750 54317 RMVar_ID_54317 Human_SNP_ID_881897437 A-to-I Human chrX - 154030432 154030432 154030432 AGGGAGAGCGCAAAGACATTGTTTCATCCTCCATGCCAAGGCCAAACAGAGAGGAGCCTGTGGAC AGGGAGAGCGCAAAGACATTGTTTCATCCTCCTTGCCAAGGCCAAACAGAGAGGAGCCTGTGGAC T A MECP2 Ensembl:ENSG00000169057 Protein coding CDS GSE100210 HepG2 cell line chrX:154030431..154030432 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC 33..33 33 LIHC 2 - Human_RBP_ID_731548,Human_RBP_ID_3977764,Human_RBP_ID_7987132,Human_RBP_ID_9340085 Human_miRNA_ID_1062714 54318 RMVar_ID_54318 Human_SNP_ID_881897440 A-to-I Human chrX - 154030432 154030432 154030432 AGGGAGAGCGCAAAGACATTGTTTCATCCTCCATGCCAAGGCCAAACAGAGAGGAGCCTGTGGAC AGGGAGAGCGCAAAGACATTGTTTCATCCTCCGTGCCAAGGCCAAACAGAGAGGAGCCTGTGGAC T C MECP2 Ensembl:ENSG00000169057 Protein coding CDS GSE100210 HepG2 cell line chrX:154030431..154030432 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_731548,Human_RBP_ID_3977764,Human_RBP_ID_7987132,Human_RBP_ID_9340085 Human_miRNA_ID_1062714 54319 RMVar_ID_54319 Human_SNP_ID_881912802 A-to-I Human chrX - 150232161 150232161 150232161 CAGCAAGCTAGAAGACCTGTTGCAGAAGGTTCACGCCAAAGAGACCAGGAAGCGAGCACTCAGCA CAGCAAGCTAGAAGACCTGTTGCAGAAGGTTCGCGCCAAAGAGACCAGGAAGCGAGCACTCAGCA T C XRCC6P2 Ensembl:ENSG00000234825 Pseudogene exon GSE100210 HepG2 cell line chrX:150232160..150232161 29129909 RNA-Seq:(High) rs782054511 Functional Loss SNV ICGC 33..33 33 LAML 2 - 54320 RMVar_ID_54320 Human_SNP_ID_881921470 A-to-I Human chrX - 103651804 103651804 103651804 CACCATCAATTATAGCTGCTCAACGTCAAACGATATTAGCAGAATACAATATGTCTTGTGATGAT CACCATCAATTATAGCTGCTCAACGTCAAACGGTATTAGCAGAATACAATATGTCTTGTGATGAT T C AL049610.1 Ensembl:ENSG00000180284 Pseudogene exon GSE100210 HepG2 cell line chrX:103651803..103651804 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_miRNA_ID_1910807 54321 RMVar_ID_54321 Human_SNP_ID_881934467 A-to-I Human chrX + 93223753 93223753 93223753 TAGAGTGGCAATGATACTTTCATACTTGTTGGAGTATTTGCGGAAGATGTCCCTGATGACAACAA TAGAGTGGCAATGATACTTTCATACTTGTTGGGGTATTTGCGGAAGATGTCCCTGATGACAACAA A G - - Other Unknown GSE100210 HepG2 cell line chrX:93223752..93223753 29129909 RNA-Seq:(High) rs878960852 Functional Loss SNV ICGC 33..33 33 LAML 2 - 54322 RMVar_ID_54322 Human_SNP_ID_881938336 A-to-I Human chrX - 74197710 74197710 74197710 GCTGGAATTTCCACATGCAAAAGAATGAAATTAGACTCTTACATTACACCATACACAAAAATCAA GCTGGAATTTCCACATGCAAAAGAATGAAATTTGACTCTTACATTACACCATACACAAAAATCAA T A FTX Ensembl:ENSG00000230590 lincRNA intron GSE107867 ASD brains,temporal_cortex chrX:74197709..74197710 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_3264403,Human_RBP_ID_5108244 54323 RMVar_ID_54323 Human_SNP_ID_881996665 A-to-I Human chrX - 93224277 93224277 93224277 GGCTCAGAGCATCTGTGAGCGGGTAACTCCCCAGCTATCCCATGCCAACTCAGCAGTGGTGCTTT GGCTCAGAGCATCTGTGAGCGGGTAACTCCCCGGCTATCCCATGCCAACTCAGCAGTGGTGCTTT T C AL359263.1 Ensembl:ENSG00000234130 Pseudogene exon GSE100210 HepG2 cell line chrX:93224276..93224277 29129909 RNA-Seq:(High) rs905357924 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_17443178,Human_RBP_ID_22413435 Human_miRNA_ID_1853728,Human_miRNA_ID_1863804,Human_miRNA_ID_1879266,Human_miRNA_ID_1904300 54324 RMVar_ID_54324 Human_SNP_ID_882133399 A-to-I Human chrX - 75742164 75742164 75742164 GAAGAAGAAAATTAAAAAGGTTTCAAATGCCAATGAAATGTATACCCAGAAAAATGATGGAAACG GAAGAAGAAAATTAAAAAGGTTTCAAATGCCAGTGAAATGTATACCCAGAAAAATGATGGAAACG T C TTC3P1 Ensembl:ENSG00000215105 Pseudogene exon GSE107867 ASD brains,cerebellum chrX:75742163..75742164 30559470 RNA-Seq:(High) rs1431683166 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_3932049 54325 RMVar_ID_54325 Human_SNP_ID_882136456 A-to-I Human chrX - 75742452 75742452 75742452 CAATACTGAGCCATATAATCCTTTTGAGAAACAACAAGGGGAAATTTCACGGATTGAAAAGGAGT CAATACTGAGCCATATAATCCTTTTGAGAAACGACAAGGGGAAATTTCACGGATTGAAAAGGAGT T C TTC3P1 Ensembl:ENSG00000215105 Pseudogene exon GSE100210 HepG2 cell line chrX:75742451..75742452 29129909 RNA-Seq:(High) rs878937285 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_3932049 54326 RMVar_ID_54326 Human_SNP_ID_882200777 A-to-I Human chrX + 75584935 75584935 75584935 GACCACTCTTTCCCCAAATTCTCACCTCTATTAAGCTGCTGACCCGCTCATTGCCAAAAATTCAC GACCACTCTTTCCCCAAATTCTCACCTCTATTGAGCTGCTGACCCGCTCATTGCCAAAAATTCAC A G BRAFP1 Ensembl:ENSG00000224775 Pseudogene exon GSE100210 HepG2 cell line chrX:75584934..75584935 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_9250530 RMVar_hsa_circ_263073 54327 RMVar_ID_54327 Human_SNP_ID_882216870 A-to-I Human chrX - 55749905 55749905 55749905 GGTCTCTGGTTTTCCTAGGCAGAGGACCCTGCAGCCTTCCGCAGTGTTTGTGTCCCTGGGTACTT GGTCTCTGGTTTTCCTAGGCAGAGGACCCTGCGGCCTTCCGCAGTGTTTGTGTCCCTGGGTACTT T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chrX:55749904..55749905 30559470 RNA-Seq:(High) rs1441730615 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 54328 RMVar_ID_54328 Human_SNP_ID_882237483 A-to-I Human chrX + 75746060 75746060 75746060 TTCTTCAGAATAGTGGCTCTCTTTCCATCACCAAGTGCATTTCTAAACTGTCCAGTACGAAGAAA TTCTTCAGAATAGTGGCTCTCTTTCCATCACCGAGTGCATTTCTAAACTGTCCAGTACGAAGAAA A G lnc-UPRT-6,lnc-UPRT-6:2 RNACentral:URS0000D5A8D3,RNACentral:URS0000D59F2E lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line chrX:75746059..75746060 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 2 - 54329 RMVar_ID_54329 Human_SNP_ID_882333463 A-to-I Human chrX - 103651809 103651809 103651809 AGTTGCACCATCAATTATAGCTGCTCAACGTCAAACGATATTAGCAGAATACAATATGTCTTGTG AGTTGCACCATCAATTATAGCTGCTCAACGTCGAACGATATTAGCAGAATACAATATGTCTTGTG T C AL049610.1 Ensembl:ENSG00000180284 Pseudogene exon GSE100210 HepG2 cell line chrX:103651808..103651809 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_miRNA_ID_1910807 54330 RMVar_ID_54330 Human_SNP_ID_882362707 A-to-I Human chrX + 75741689 75741689 75741689 TCATCATGGCCTGAAGACTCAGGGAGTAACTCAGGATGAACCGTGTTACAGGCAGGAAATGAAAG TCATCATGGCCTGAAGACTCAGGGAGTAACTCGGGATGAACCGTGTTACAGGCAGGAAATGAAAG A G lnc-UPRT-6,lnc-UPRT-6:2 RNACentral:URS0000D5A8D3,RNACentral:URS0000D59F2E lincRNA,lincRNA intron,intron GSE100210 HepG2 cell line chrX:75741688..75741689 29129909 RNA-Seq:(High) rs761200900 Functional Loss SNV ICGC 33..33 33 LAML 2 - 54331 RMVar_ID_54331 Human_SNP_ID_882378078 A-to-I Human chrX + 17379501 17379501 17379501 AAGCTTAAATAACTTGTAGACTGTGGCTGGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTG AAGCTTAAATAACTTGTAGACTGTGGCTGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTG A G NHS Ensembl:ENSG00000188158 Protein coding intron GSE100210 HepG2 cell line chrX:17379500..17379501 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BOCA 1 - Human_RBP_ID_188772 54332 RMVar_ID_54332 Human_SNP_ID_882390223 A-to-I Human chrX - 93224311 93224311 93224311 GCCTGTCTAATTACAACCCTAAAAATGATCGGAAGGCTCAGAGCATCTGTGAGCGGGTAACTCCC GCCTGTCTAATTACAACCCTAAAAATGATCGGGAGGCTCAGAGCATCTGTGAGCGGGTAACTCCC T C AL359263.1 Ensembl:ENSG00000234130 Pseudogene exon GSE100210 HepG2 cell line chrX:93224310..93224311 29129909 RNA-Seq:(High) rs1382016416 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_17443178,Human_RBP_ID_22413355 Human_miRNA_ID_1895876,Human_miRNA_ID_1905128 54333 RMVar_ID_54333 Human_SNP_ID_882520578 A-to-I Human chrX + 85091329 85091329 85091329 GATGAAATATGAGTGTGTTTGAGATCTGATCCAAGGTTTTAAAAAATTCATTTCAAATCCTGGAG GATGAAATATGAGTGTGTTTGAGATCTGATCCTAGGTTTTAAAAAATTCATTTCAAATCCTGGAG A T APOOL Ensembl:ENSG00000155008 Protein coding 3'UTR GSE38233;GSE100210 cultured B-cells;HepG2 cell line chrX:85091328..85091329 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 RECA 1 - Human_RBP_ID_26574251 54334 RMVar_ID_54334 Human_SNP_ID_882537501 A-to-I Human chrX + 85091301 85091301 85091301 ATAAAGGTATATAATATGTCTTAGATTTGATGAAATATGAGTGTGTTTGAGATCTGATCCAAGGT ATAAAGGTATATAATATGTCTTAGATTTGATGGAATATGAGTGTGTTTGAGATCTGATCCAAGGT A G APOOL Ensembl:ENSG00000155008 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells chrX:85091301..85091302 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_26574251 54335 RMVar_ID_54335 Human_SNP_ID_882545901 A-to-I Human chrX - 85863096 85863095 85863097 AGAGCAAGACTCTGTCTCACAAAAAAAAAAAAAGGGGGCTGTACATAGGCAGCAAACTAAGCTGC AGAGCAAGACTCTGTCTCACAAAAAAAAAAA__GGGGGCTGTACATAGGCAGCAAACTAAGCTGC CTT C CHM Ensembl:ENSG00000188419 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line chrX:85863095..85863096 31158229 RNA-Seq:(High) - Functional Loss DEL TCGA 32..33 33 UCEC 1 - Human_RBP_ID_740400 Human_miRNA_ID_187909 54336 RMVar_ID_54336 Human_SNP_ID_882549963 A-to-I Human chrX - 68070651 68070651 68070651 CTAGGGGCTGCATTACCATCATAGGTGGTGGAAACACTGCCACTTGCTGTGCCAAATGGAACACA CTAGGGGCTGCATTACCATCATAGGTGGTGGAGACACTGCCACTTGCTGTGCCAAATGGAACACA T C AL158201.1,OPHN1 Ensembl:ENSG00000228328,Ensembl:ENSG00000079482 Pseudogene,Protein coding exon,intron GSE100210 HepG2 cell line chrX:68070650..68070651 29129909 RNA-Seq:(High) rs879164909 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_22413407 Human_miRNA_ID_1860718,Human_miRNA_ID_1861162,Human_miRNA_ID_1875221,Human_miRNA_ID_1875501 RMVar_hsa_circ_89329,RMVar_hsa_circ_262797,RMVar_hsa_circ_125754,RMVar_hsa_circ_262799,RMVar_hsa_circ_378257,RMVar_hsa_circ_262800,RMVar_hsa_circ_343911,RMVar_hsa_circ_293079,RMVar_hsa_circ_294332,RMVar_hsa_circ_345613,RMVar_hsa_circ_289141,RMVar_hsa_circ_262805,RMVar_hsa_circ_36151,RMVar_hsa_circ_39994,RMVar_hsa_circ_262806,RMVar_hsa_circ_262807,RMVar_hsa_circ_262804 54337 RMVar_ID_54337 Human_SNP_ID_882649607 A-to-I Human chrX + 70857601 70857601 70857601 GATATGTCATATATCTCAAAATGGTTCAAGTGAGTGTACCAGTGATGGCAATAAGAAAAATGATA GATATGTCATATATCTCAAAATGGTTCAAGTGGGTGTACCAGTGATGGCAATAAGAAAAATGATA A G - - Other Unknown GSE38233 cultured B-cells chrX:70857600..70857601 24183664 RNA-Seq:(High) rs1191033548 Functional Loss SNV ICGC 33..33 33 LAML 1 - 54338 RMVar_ID_54338 Human_SNP_ID_882655590 A-to-I Human chrX + 93223730 93223730 93223730 TCCAGCGAGTCTAAGTTCTCACATAGAGTGGCAATGATACTTTCATACTTGTTGGAGTATTTGCG TCCAGCGAGTCTAAGTTCTCACATAGAGTGGCGATGATACTTTCATACTTGTTGGAGTATTTGCG A G - - Other Unknown GSE100210 HepG2 cell line chrX:93223729..93223730 29129909 RNA-Seq:(High) rs879231422 Functional Loss SNV ICGC 33..33 33 LAML 1 - 54339 RMVar_ID_54339 Human_SNP_ID_882680669 A-to-I Human chrX - 64916885 64916885 64916885 GCTCAATGGTATATTGCAGGGAGGAGAGGAGTAGATTTAGATTTGAGTAAATGCCAATCACTTTA GCTCAATGGTATATTGCAGGGAGGAGAGGAGTTGATTTAGATTTGAGTAAATGCCAATCACTTTA T A ZC4H2 Ensembl:ENSG00000126970 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector chrX:64916884..64916885 29967493 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - 54340 RMVar_ID_54340 Human_SNP_ID_882686175 A-to-I Human chrX - 11407375 11407375 11407375 TCCATCCTAACTGATTAACAGATAAACAAAATATGGTCAACCATACAAGAGAATATTATTCAATA TCCATCCTAACTGATTAACAGATAAACAAAATTTGGTCAACCATACAAGAGAATATTATTCAATA T A ARHGAP6 Ensembl:ENSG00000047648 Protein coding intron GSE100210 HepG2 cell line chrX:11407374..11407375 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 54341 RMVar_ID_54341 Human_SNP_ID_882867406 A-to-I Human chrX - 93223552 93223552 93223552 CCCAGGTGCAGCTCACTCTGCTTACTGCCATAATGAAGCTGTTTCTCAAGAAACCACCAAAACAC CCCAGGTGCAGCTCACTCTGCTTACTGCCATAGTGAAGCTGTTTCTCAAGAAACCACCAAAACAC T C AL359263.1 Ensembl:ENSG00000234130 Pseudogene exon GSE100210 HepG2 cell line chrX:93223551..93223552 29129909 RNA-Seq:(High) rs1325408733 Functional Loss SNV ICGC 33..33 33 LAML 2 - 54342 RMVar_ID_54342 Human_SNP_ID_882962938 A-to-I Human chrX - 57393843 57393843 57393843 ATCCAGAAACCATAGCTTGGCAAAGAGTGTTGAATACCAATGATAGATTCCTGAGGAAGATCACG ATCCAGAAACCATAGCTTGGCAAAGAGTGTTGGATACCAATGATAGATTCCTGAGGAAGATCACG T C MTHFD1P1 Ensembl:ENSG00000231831 Pseudogene exon GSE100210 HepG2 cell line chrX:57393842..57393843 29129909 RNA-Seq:(High) rs1197828090 Functional Loss SNV ICGC 33..33 33 LAML 1 - 54343 RMVar_ID_54343 Human_SNP_ID_882963042 A-to-I Human chrX - 74277900 74277900 74277900 GGGTCTTGCTCTATCTCCCAGGCTGGAGTGCAATGGTGCGATCACAGCTCACTGCAGCCTCAACC GGGTCTTGCTCTATCTCCCAGGCTGGAGTGCAGTGGTGCGATCACAGCTCACTGCAGCCTCAACC T C FTX Ensembl:ENSG00000230590 lincRNA intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chrX:74277899..74277900 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - Human_RBP_ID_16939861 RMVar_hsa_circ_335579,RMVar_hsa_circ_342788 54344 RMVar_ID_54344 Human_SNP_ID_883011425 A-to-I Human chrX - 46419263 46419263 46419263 CCATATTGCTCCAGGACAATGATGAAAACAGGAAATTGCTTGGGGAGCTGGATAGAATTGATGCA CCATATTGCTCCAGGACAATGATGAAAACAGGGAATTGCTTGGGGAGCTGGATAGAATTGATGCA T C AL139811.2 Ensembl:ENSG00000231235 Pseudogene exon GSE100210 HepG2 cell line chrX:46419262..46419263 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 1 - 54345 RMVar_ID_54345 Human_SNP_ID_883033140 A-to-I Human chrX - 154011114 154011114 154011114 TATGACTGCACTCCAGCCTGGGTGACAGAGCAAGACCCTGTTTCAAAAAGAAAAACCCTGGGAAA TATGACTGCACTCCAGCCTGGGTGACAGAGCACGACCCTGTTTCAAAAAGAAAAACCCTGGGAAA T G IRAK1 Ensembl:ENSG00000184216 Protein coding 3'UTR GSE100210 HepG2 cell line chrX:154011113..154011114 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LMS 1 - Human_RBP_ID_731412,Human_RBP_ID_5056827,Human_RBP_ID_9244849,Human_RBP_ID_16847633,Human_RBP_ID_24334771,Human_RBP_ID_27163353 Human_Splice_Rec_2246908 Human_miRNA_ID_475585,Human_miRNA_ID_1266518,Human_miRNA_ID_2158304,Human_miRNA_ID_2611936,Human_miRNA_ID_2908992,Human_miRNA_ID_3027836 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 54346 RMVar_ID_54346 Human_SNP_ID_883146804 A-to-I Human chrX + 57393611 57393611 57393611 GATTGGGCTTGATTGTGTCCTTCATAAGCACTATCAATGCACCACTCACCCCCAGATCTTCAGCA GATTGGGCTTGATTGTGTCCTTCATAAGCACTGTCAATGCACCACTCACCCCCAGATCTTCAGCA A G FAAH2 Ensembl:ENSG00000165591 Protein coding intron GSE100210 HepG2 cell line chrX:57393610..57393611 29129909 RNA-Seq:(High) rs1419238515 Functional Loss SNV ICGC 33..33 33 LAML 1 - RMVar_hsa_circ_6235,RMVar_hsa_circ_262686,RMVar_hsa_circ_262687 54347 RMVar_ID_54347 Human_SNP_ID_883168565 A-to-I Human chrX + 75584944 75584944 75584944 TTCCCCAAATTCTCACCTCTATTAAGCTGCTGACCCGCTCATTGCCAAAAATTCACCACAGTGCA TTCCCCAAATTCTCACCTCTATTAAGCTGCTGGCCCGCTCATTGCCAAAAATTCACCACAGTGCA A G BRAFP1 Ensembl:ENSG00000224775 Pseudogene exon GSE100210 HepG2 cell line chrX:75584943..75584944 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 1 - RMVar_hsa_circ_263073 54348 RMVar_ID_54348 Human_SNP_ID_883168596 A-to-I Human chrX - 103651815 103651815 103651815 GAGAGTAGTTGCACCATCAATTATAGCTGCTCAACGTCAAACGATATTAGCAGAATACAATATGT GAGAGTAGTTGCACCATCAATTATAGCTGCTCGACGTCAAACGATATTAGCAGAATACAATATGT T C AL049610.1 Ensembl:ENSG00000180284 Pseudogene exon GSE100210 HepG2 cell line chrX:103651814..103651815 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_miRNA_ID_1910807 54349 RMVar_ID_54349 Human_SNP_ID_883170249 A-to-I Human chrX + 46547980 46547980 46547980 AAGTGTGCGCCACCACACCTGGCTAATTTTTTAAATTTTTTGTAGAGATAGTGTCTCGCTATGTT AAGTGTGCGCCACCACACCTGGCTAATTTTTTTAATTTTTTGTAGAGATAGTGTCTCGCTATGTT A T ZNF674-AS1 Ensembl:ENSG00000230844 lincRNA exon GSE100210 HepG2 cell line chrX:46547979..46547980 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_16963715 54350 RMVar_ID_54350 Human_SNP_ID_883225680 A-to-I Human chrX - 53546536 53546536 53546536 GAGGAAGGCTTAGAGGATGCAGCCAACGTACTACTGCAGCTCTCCCGGGGGGACTCTGGGACCCG GAGGAAGGCTTAGAGGATGCAGCCAACGTACTGCTGCAGCTCTCCCGGGGGGACTCTGGGACCCG T C HUWE1 Ensembl:ENSG00000086758 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector chrX:53546535..53546536 29967493 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC 33..33 33 COAD,OV 3 - Human_RBP_ID_1062931,Human_RBP_ID_1071016,Human_RBP_ID_2075823,Human_RBP_ID_5083478,Human_RBP_ID_8009315,Human_RBP_ID_8936462,Human_RBP_ID_9317957,Human_RBP_ID_17326657,Human_RBP_ID_17554888,Human_RBP_ID_18152299,Human_RBP_ID_18197323,Human_RBP_ID_18405953 Human_Splice_Rec_2209018,Human_Splice_Rec_2209175,Human_Splice_Rec_2209337,Human_Splice_Rec_2209502,Human_Splice_Rec_2209542,Human_Splice_Rec_2209552 Human_miRNA_ID_2174108,Human_miRNA_ID_2177552,Human_miRNA_ID_2356049,Human_miRNA_ID_3011907 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_363826,RMVar_hsa_circ_75758,RMVar_hsa_circ_5290,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_262518,RMVar_hsa_circ_262520,RMVar_hsa_circ_85924,RMVar_hsa_circ_262519,RMVar_hsa_circ_335666,RMVar_hsa_circ_126578,RMVar_hsa_circ_12232,RMVar_hsa_circ_111209,RMVar_hsa_circ_348852,RMVar_hsa_circ_262522,RMVar_hsa_circ_262523,RMVar_hsa_circ_40487,RMVar_hsa_circ_103982,RMVar_hsa_circ_262524,RMVar_hsa_circ_262525,RMVar_hsa_circ_88917,RMVar_hsa_circ_90734,RMVar_hsa_circ_124425,RMVar_hsa_circ_262526,RMVar_hsa_circ_262528,RMVar_hsa_circ_262529 54351 RMVar_ID_54351 Human_SNP_ID_883259936 A-to-I Human chrX + 107131998 107131998 107131998 AGAAGAAGGAAGGAGAAGAAAACATAGGTGGGATGGAATGGTTGCAAATAAAGGATAATGATTTC AGAAGAAGGAAGGAGAAGAAAACATAGGTGGGGTGGAATGGTTGCAAATAAAGGATAATGATTTC A G AL390039.1 Ensembl:ENSG00000213569 Pseudogene exon GSE100210 HepG2 cell line chrX:107131997..107131998 29129909 RNA-Seq:(High) rs879156619 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_17443186,Human_RBP_ID_18543428 54352 RMVar_ID_54352 Human_SNP_ID_883343020 A-to-I Human chrX - 93224320 93224320 93224320 TGCTGGACTGCCTGTCTAATTACAACCCTAAAAATGATCGGAAGGCTCAGAGCATCTGTGAGCGG TGCTGGACTGCCTGTCTAATTACAACCCTAAAGATGATCGGAAGGCTCAGAGCATCTGTGAGCGG T C AL359263.1 Ensembl:ENSG00000234130 Pseudogene exon GSE100210 HepG2 cell line chrX:93224319..93224320 29129909 RNA-Seq:(High) rs1405497186 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_22413355 Human_miRNA_ID_1895876,Human_miRNA_ID_1905128 54353 RMVar_ID_54353 Human_SNP_ID_883343998 A-to-I Human chrX + 134843089 134843089 134843089 GGGCCTGGTGGCATGCGCCTGTAATCCAAGCTACTCAGGAGGCTGAGACAGGAGAATCGCTTGAA GGGCCTGGTGGCATGCGCCTGTAATCCAAGCTGCTCAGGAGGCTGAGACAGGAGAATCGCTTGAA A G FAM122C Ensembl:ENSG00000156500 Protein coding intron GSE100210 HepG2 cell line chrX:134843088..134843089 29129909 RNA-Seq:(High) rs1445054652 Functional Loss SNV ICGC 33..33 33 LAML 1 - 54354 RMVar_ID_54354 Human_SNP_ID_806345702 A-to-I Human chr10 - 103306853 103306853 103306853 GTGATCCACCTGCCTTGGCCTCCCAAAGTGCTAGGATTATAGGCATGAGCCCCTGCACCTGGCCT GTGATCCACCTGCCTTGGCCTCCCAAAGTGCTGGGATTATAGGCATGAGCCCCTGCACCTGGCCT T C PCGF6 Ensembl:ENSG00000156374 Protein coding intron GSE100210 HepG2 cell line chr10:103306852..103306853 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - RMVar_hsa_circ_96751,RMVar_hsa_circ_124980,RMVar_hsa_circ_146039,RMVar_hsa_circ_146040 54355 RMVar_ID_54355 Human_SNP_ID_806367664 A-to-I Human chr10 + 68789111 68789111 68789111 TTTTGTATTTTTAGTAGAGACAGGGTTTCACCATGTTTGCTAGGATGGTCTCGATCTCCTGACCT TTTTGTATTTTTAGTAGAGACAGGGTTTCACCTTGTTTGCTAGGATGGTCTCGATCTCCTGACCT A T CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE47997 K562 cells&HepG2 cells chr10:68789110..68789111 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 4 pancreas RMVar_hsa_circ_115064,RMVar_hsa_circ_143888,RMVar_hsa_circ_268652,RMVar_hsa_circ_143906,RMVar_hsa_circ_69537,RMVar_hsa_circ_143913,RMVar_hsa_circ_272077,RMVar_hsa_circ_143914,RMVar_hsa_circ_143917,RMVar_hsa_circ_56157,RMVar_hsa_circ_308425,RMVar_hsa_circ_143918,RMVar_hsa_circ_310182 54356 RMVar_ID_54356 Human_SNP_ID_806413488 A-to-I Human chr10 - 131959411 131959411 131959411 CATCTCCACAGGGGGATGGGGGATCAGCACACACCTTCATCTCCACAGTGGGATGGCGGATCAGC CATCTCCACAGGGGGATGGGGGATCAGCACACGCCTTCATCTCCACAGTGGGATGGCGGATCAGC T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr10:131959410..131959411 30559470 RNA-Seq:(High) rs1286737612 Functional Loss SNV ICGC 33..33 33 STAD 1 - 54357 RMVar_ID_54357 Human_SNP_ID_806423217 A-to-I Human chr10 - 67819077 67819077 67819077 CGCCCGCCTCGGTCTCCCAGAGTCCTGGGATTACAGGCGTGAGCCACCGCTCCCGACCCCTGGCC CGCCCGCCTCGGTCTCCCAGAGTCCTGGGATTGCAGGCGTGAGCCACCGCTCCCGACCCCTGGCC T C DNAJC12 Ensembl:ENSG00000108176 Protein coding intron GSE100210 HepG2 cell line chr10:67819076..67819077 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - RMVar_hsa_circ_143654,RMVar_hsa_circ_340263 54358 RMVar_ID_54358 Human_SNP_ID_806444023 A-to-I Human chr10 - 100233141 100233141 100233141 TTTTTTTAATTAAAAGAATTTTTTTTGAGACAAAGTCTCGCTCTGTCACCCAAGCAGGATTGCAG TTTTTTTAATTAAAAGAATTTTTTTTGAGACACAGTCTCGCTCTGTCACCCAAGCAGGATTGCAG T G CWF19L1 Ensembl:ENSG00000095485 Protein coding 3'UTR GSE100210 HepG2 cell line chr10:100233140..100233141 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA 33..33 33 UCEC 1 - Human_RBP_ID_11229643,Human_RBP_ID_26391550,Human_RBP_ID_26872821 Human_Splice_Rec_1168073 54359 RMVar_ID_54359 Human_SNP_ID_806468328 A-to-I Human chr10 + 68759390 68759390 68759390 TGAACTATCATTGTGCCACTGTACTCCAGCCTAGGCAACAAAATGAAATCCTGTCTAAAAATAAA TGAACTATCATTGTGCCACTGTACTCCAGCCTGGGCAACAAAATGAAATCCTGTCTAAAAATAAA A G CCAR1,AL513534.2 Ensembl:ENSG00000060339,Ensembl:ENSG00000221184 Protein coding,miRNA intron,exon GSE38233;GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line chr10:68759389..68759390 24183664,29129909,31158229 RNA-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_11401596,Human_RBP_ID_18510502 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_52772,RMVar_hsa_circ_308624 54360 RMVar_ID_54360 Human_SNP_ID_806482725 A-to-I Human chr10 - 119573096 119573096 119573096 CCGCCTCAGTCTCCCAAAGTGCTGGGACTACAAGCGTGAGCCACGGTGTCTGGCTTTTTTTTTTT CCGCCTCAGTCTCCCAAAGTGCTGGGACTACATGCGTGAGCCACGGTGTCTGGCTTTTTTTTTTT T A TIAL1 Ensembl:ENSG00000151923 Protein coding 3'UTR GSE100210 HepG2 cell line chr10:119573095..119573096 29129909 RNA-Seq:(High) rs1307002967 Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 2 breast 54361 RMVar_ID_54361 Human_SNP_ID_806518798 A-to-I Human chr10 - 15520182 15520182 15520182 GTCTCGACCTCCTGAGCTCAGGCAATCCACCCACCTTGGCCTCCCAAAGTGCTAGGATTACAGGC GTCTCGACCTCCTGAGCTCAGGCAATCCACCCGCCTTGGCCTCCCAAAGTGCTAGGATTACAGGC T C ITGA8 Ensembl:ENSG00000077943 Protein coding intron GSE47997 K562 cells&HepG2 cells chr10:15520181..15520182 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - RMVar_hsa_circ_38733 54362 RMVar_ID_54362 Human_SNP_ID_806527712 A-to-I Human chr10 - 14005090 14005090 14005090 TGAACCTGGGAGGTGGAGGTTGCTGTGAGCCAAGATGGAGCCACTGCACTCGAGCCTGGTGACAG TGAACCTGGGAGGTGGAGGTTGCTGTGAGCCAGGATGGAGCCACTGCACTCGAGCCTGGTGACAG T C FRMD4A Ensembl:ENSG00000151474 Protein coding intron GSE107867 ASD brains,temporal_cortex chr10:14005089..14005090 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_3651 54363 RMVar_ID_54363 Human_SNP_ID_806537311 A-to-I Human chr10 - 48450444 48450444 48450444 CTCCCCGCTCCCCAGCAGCAGCGAGGACCCCAAGTCCCTGGACCTGGACCACAGCATGGACGAGG CTCCCCGCTCCCCAGCAGCAGCGAGGACCCCACGTCCCTGGACCTGGACCACAGCATGGACGAGG T G ARHGAP22 Ensembl:ENSG00000128805 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector chr10:48450443..48450444 29967493 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 mouth squamous_cell_carcinoma 7 head and neck 54364 RMVar_ID_54364 Human_SNP_ID_806538004 A-to-I Human chr10 - 114471031 114471031 114471031 AAAATACAAAAATTAGCCAGGAATGATGGCACACGCCTGTAGTCCCAGCAACTTGGGAGGCTGAG AAAATACAAAAATTAGCCAGGAATGATGGCACGCGCCTGTAGTCCCAGCAACTTGGGAGGCTGAG T C ABLIM1 Ensembl:ENSG00000099204 Protein coding intron GSE107867 ASD brains,cerebellum chr10:114471030..114471031 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 UTCA,endometrium carcinosarcoma-malignant_mesodermal_mixed_tumour 17 uterus RMVar_hsa_circ_34764,RMVar_hsa_circ_107118,RMVar_hsa_circ_122800,RMVar_hsa_circ_101470,RMVar_hsa_circ_146457,RMVar_hsa_circ_89929,RMVar_hsa_circ_146455,RMVar_hsa_circ_146456,RMVar_hsa_circ_146454,RMVar_hsa_circ_53410,RMVar_hsa_circ_20409,RMVar_hsa_circ_72075,RMVar_hsa_circ_115438,RMVar_hsa_circ_146466,RMVar_hsa_circ_300141,RMVar_hsa_circ_377515,RMVar_hsa_circ_283245,RMVar_hsa_circ_40012,RMVar_hsa_circ_51283,RMVar_hsa_circ_146471,RMVar_hsa_circ_359623 54365 RMVar_ID_54365 Human_SNP_ID_806576157 A-to-I Human chr10 + 112449969 112449969 112449969 TCGCCCACGTTGGAGTGTAATGGCGCAATCTCAGCTCATTGCAACCTCTCCCTCACGGCTCAAGT TCGCCCACGTTGGAGTGTAATGGCGCAATCTCTGCTCATTGCAACCTCTCCCTCACGGCTCAAGT A T VTI1A Ensembl:ENSG00000151532 Protein coding exon GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr10:112449968..112449969 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_370172 54366 RMVar_ID_54366 Human_SNP_ID_806667995 A-to-I Human chr10 - 17577587 17577587 17577587 AATGCCTGTTAGCCTCACGTAAAATGCCCCCAACATGCGGACATACTTGAAATCTTCATTTTTGA AATGCCTGTTAGCCTCACGTAAAATGCCCCCAGCATGCGGACATACTTGAAATCTTCATTTTTGA T C - - Other Unknown GSE100210 HepG2 cell line chr10:17577586..17577587 29129909 RNA-Seq:(High) rs1297698710 Functional Loss SNV ICGC 33..33 33 LAML 2 - RMVar_hsa_circ_142460,RMVar_hsa_circ_142461 54367 RMVar_ID_54367 Human_SNP_ID_806717588 A-to-I Human chr10 - 63192481 63192481 63192481 TCACTGCAATCTCTGCCTCCCAGGTTTAAGTGATTGTCCTGCCTCAGCCTCCCAAGTAGATGGGA TCACTGCAATCTCTGCCTCCCAGGTTTAAGTGGTTGTCCTGCCTCAGCCTCCCAAGTAGATGGGA T C JMJD1C Ensembl:ENSG00000171988 Protein coding intron GSE38233 cultured B-cells chr10:63192480..63192481 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_997,RMVar_hsa_circ_107684,RMVar_hsa_circ_143592,RMVar_hsa_circ_301264,RMVar_hsa_circ_301919,RMVar_hsa_circ_283354,RMVar_hsa_circ_25346,RMVar_hsa_circ_48453,RMVar_hsa_circ_143600,RMVar_hsa_circ_143601,RMVar_hsa_circ_143599,RMVar_hsa_circ_313931,RMVar_hsa_circ_45395,RMVar_hsa_circ_68260,RMVar_hsa_circ_8169,RMVar_hsa_circ_143604,RMVar_hsa_circ_296902,RMVar_hsa_circ_143603,RMVar_hsa_circ_318595,RMVar_hsa_circ_365973,RMVar_hsa_circ_143605,RMVar_hsa_circ_269563,RMVar_hsa_circ_286318,RMVar_hsa_circ_321468,RMVar_hsa_circ_269598,RMVar_hsa_circ_143609,RMVar_hsa_circ_7067,RMVar_hsa_circ_143610,RMVar_hsa_circ_331076,RMVar_hsa_circ_66718,RMVar_hsa_circ_143611,RMVar_hsa_circ_54395,RMVar_hsa_circ_322304,RMVar_hsa_circ_327043,RMVar_hsa_circ_352499,RMVar_hsa_circ_61924,RMVar_hsa_circ_266962,RMVar_hsa_circ_35036,RMVar_hsa_circ_68824,RMVar_hsa_circ_143613,RMVar_hsa_circ_143614,RMVar_hsa_circ_350821,RMVar_hsa_circ_309240,RMVar_hsa_circ_143616,RMVar_hsa_circ_19441,RMVar_hsa_circ_143615 54368 RMVar_ID_54368 Human_SNP_ID_806717822 A-to-I Human chr10 + 63140027 63140027 63140027 GAGCATGGTGGCACATGTCTGTGGTTCCAGCTACTTGAGAGGCTGAGATAGGAGGATCACTTGAG GAGCATGGTGGCACATGTCTGTGGTTCCAGCTGCTTGAGAGGCTGAGATAGGAGGATCACTTGAG A G NRBF2 Ensembl:ENSG00000148572 Protein coding intron GSE38233 cultured B-cells chr10:63140026..63140027 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_126098,RMVar_hsa_circ_143591 54369 RMVar_ID_54369 Human_SNP_ID_806741069 A-to-I Human chr10 + 18452152 18452152 18452152 GAACAAGTCATAATAAAAATACAGCTGGGCATAGCGATGCACACCTTTAATCCCAACACTTTGGG GAACAAGTCATAATAAAAATACAGCTGGGCATGGCGATGCACACCTTTAATCCCAACACTTTGGG A G CACNB2 Ensembl:ENSG00000165995 Protein coding intron GSE100210 HepG2 cell line chr10:18452151..18452152 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - 54370 RMVar_ID_54370 Human_SNP_ID_806770089 A-to-I Human chr10 - 101810957 101810957 101810957 ATCCAGTACCATGGCTCATGCCTGCAATCCCAACACTGTAAGAGGCTAAGGCAGGCGGATCACTT ATCCAGTACCATGGCTCATGCCTGCAATCCCAGCACTGTAAGAGGCTAAGGCAGGCGGATCACTT T C OGA Ensembl:ENSG00000198408 Protein coding intron GSE47997 K562 cells&HepG2 cells chr10:101810956..101810957 23474544 RNA-Seq:(High) rs894294126 Functional Loss SNV ICGC 33..33 33 PRAD 1 - Human_RBP_ID_11238362,Human_RBP_ID_17559180 RMVar_hsa_circ_91447,RMVar_hsa_circ_145753,RMVar_hsa_circ_377677,RMVar_hsa_circ_67795,RMVar_hsa_circ_68548,RMVar_hsa_circ_332190,RMVar_hsa_circ_271818,RMVar_hsa_circ_145768,RMVar_hsa_circ_145776,RMVar_hsa_circ_273642,RMVar_hsa_circ_318924,RMVar_hsa_circ_145775,RMVar_hsa_circ_295545,RMVar_hsa_circ_327448,RMVar_hsa_circ_145777,RMVar_hsa_circ_313074,RMVar_hsa_circ_102464,RMVar_hsa_circ_145788,RMVar_hsa_circ_352986,RMVar_hsa_circ_365432,RMVar_hsa_circ_145791,RMVar_hsa_circ_11375,RMVar_hsa_circ_329858,RMVar_hsa_circ_343243,RMVar_hsa_circ_283899,RMVar_hsa_circ_95277,RMVar_hsa_circ_145795,RMVar_hsa_circ_145796 54371 RMVar_ID_54371 Human_SNP_ID_806792684 A-to-I Human chr10 - 60330724 60330724 60330724 AGATTGCTGGGTCAAACAGTATTTCTAGTTCTAGATCCTTCAGGAATCGCCACACTGTCTGCCAC AGATTGCTGGGTCAAACAGTATTTCTAGTTCTTGATCCTTCAGGAATCGCCACACTGTCTGCCAC T A ANK3 Ensembl:ENSG00000151150 Protein coding intron GSE107867 ASD brains,cerebellum chr10:60330723..60330724 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 54372 RMVar_ID_54372 Human_SNP_ID_806801855 A-to-I Human chr10 + 119105381 119105381 119105381 GCAATCATCGCTCTCTGCAGCCTCCACCTCCCAGGCCCAAACCATCCTCCCGCCTCGGCCTCCGA GCAATCATCGCTCTCTGCAGCCTCCACCTCCCGGGCCCAAACCATCCTCCCGCCTCGGCCTCCGA A G DENND10 Ensembl:ENSG00000119979 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line chr10:119105380..119105381 24183664,29129909,31158229 RNA-Seq:(High) rs1428204915 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue Human_Splice_Rec_1181022,Human_Splice_Rec_1181028,Human_Splice_Rec_1181074 54373 RMVar_ID_54373 Human_SNP_ID_806814423 A-to-I Human chr10 + 16447288 16447288 16447288 CCTAATTTTTTTTTTTTTACTTTTGTAGAGATAAGGTGTCACTGTGTTGCTCAGGTCAATGTCTT CCTAATTTTTTTTTTTTTACTTTTGTAGAGATGAGGTGTCACTGTGTTGCTCAGGTCAATGTCTT A G PTER Ensembl:ENSG00000165983 Protein coding intron GSE100210 HepG2 cell line chr10:16447288..16447289 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_11321942 54374 RMVar_ID_54374 Human_SNP_ID_806857260 A-to-I Human chr10 - 1578007 1578007 1578007 TTCCACAGTCCTGGAGGCTGGAGTCTGAGATCAGCGTGTCCACAGGGCTGGCTCTGCCTAAGGCT TTCCACAGTCCTGGAGGCTGGAGTCTGAGATCGGCGTGTCCACAGGGCTGGCTCTGCCTAAGGCT T C ADARB2 Ensembl:ENSG00000185736 Protein coding intron GSE100210 HepG2 cell line chr10:1578006..1578007 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 54375 RMVar_ID_54375 Human_SNP_ID_806927259 A-to-I Human chr10 - 101811559 101811559 101811559 AGCTGGGACTACAAGCGCGGGTCACCACACCCAGCTAATTTTTGTATATTTTGTAGAGAGAGGGG AGCTGGGACTACAAGCGCGGGTCACCACACCCGGCTAATTTTTGTATATTTTGTAGAGAGAGGGG T C OGA Ensembl:ENSG00000198408 Protein coding intron GSE38233 cultured B-cells chr10:101811558..101811559 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_5918769,Human_RBP_ID_11238386 RMVar_hsa_circ_91447,RMVar_hsa_circ_145753,RMVar_hsa_circ_377677,RMVar_hsa_circ_67795,RMVar_hsa_circ_68548,RMVar_hsa_circ_332190,RMVar_hsa_circ_271818,RMVar_hsa_circ_145768,RMVar_hsa_circ_145776,RMVar_hsa_circ_273642,RMVar_hsa_circ_318924,RMVar_hsa_circ_145775,RMVar_hsa_circ_295545,RMVar_hsa_circ_327448,RMVar_hsa_circ_145777,RMVar_hsa_circ_313074,RMVar_hsa_circ_102464,RMVar_hsa_circ_145788,RMVar_hsa_circ_352986,RMVar_hsa_circ_365432,RMVar_hsa_circ_145791,RMVar_hsa_circ_11375,RMVar_hsa_circ_329858,RMVar_hsa_circ_343243,RMVar_hsa_circ_283899,RMVar_hsa_circ_95277,RMVar_hsa_circ_145795,RMVar_hsa_circ_145796 54376 RMVar_ID_54376 Human_SNP_ID_806928482 A-to-I Human chr10 + 42104155 42104155 42104155 ATCATTGAACGGAATCGAATGGAATCATCATCAGATGGAAACGAATGGAATCATCATCGAATGGA ATCATTGAACGGAATCGAATGGAATCATCATCGGATGGAAACGAATGGAATCATCATCGAATGGA A G - - Other Unknown GSE100210 HepG2 cell line chr10:42104154..42104155 29129909 RNA-Seq:(High) rs148121689 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 54377 RMVar_ID_54377 Human_SNP_ID_806955845 A-to-I Human chr10 + 27177099 27177099 27177099 ACTCCTGACCTTGTGATCCACCCAAAGTGTTCAGCCTCCCAAAGTGCTGGGATTACAGGTATGAG ACTCCTGACCTTGTGATCCACCCAAAGTGTTCCGCCTCCCAAAGTGCTGGGATTACAGGTATGAG A C MASTL Ensembl:ENSG00000120539 Protein coding intron GSE38233 cultured B-cells chr10:27177098..27177099 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_366834,RMVar_hsa_circ_326591,RMVar_hsa_circ_142821,RMVar_hsa_circ_142822,RMVar_hsa_circ_51633,RMVar_hsa_circ_323753,RMVar_hsa_circ_142832,RMVar_hsa_circ_280240,RMVar_hsa_circ_142835,RMVar_hsa_circ_279663,RMVar_hsa_circ_303255,RMVar_hsa_circ_142836,RMVar_hsa_circ_281255,RMVar_hsa_circ_142838 54378 RMVar_ID_54378 Human_SNP_ID_806984858 A-to-I Human chr10 + 11192896 11192896 11192896 TGAAGGTATTGAGGTGATTCTAACGTGCAGCCAAGGTTGAGAAGGACCAAGCTGGACGTTGCGAG TGAAGGTATTGAGGTGATTCTAACGTGCAGCCGAGGTTGAGAAGGACCAAGCTGGACGTTGCGAG A G CELF2 Ensembl:ENSG00000048740 Protein coding intron GSE107867 ASD brains,frontal_cortex chr10:11192896..11192897 30559470 RNA-Seq:(High) rs1998860 Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 16 pancreas RMVar_hsa_circ_40847,RMVar_hsa_circ_45624,RMVar_hsa_circ_314771,RMVar_hsa_circ_32203,RMVar_hsa_circ_1165,RMVar_hsa_circ_297045,RMVar_hsa_circ_305567,RMVar_hsa_circ_315228,RMVar_hsa_circ_316652,RMVar_hsa_circ_314061,RMVar_hsa_circ_34250,RMVar_hsa_circ_270630,RMVar_hsa_circ_16892,RMVar_hsa_circ_141973,RMVar_hsa_circ_141975,RMVar_hsa_circ_141976,RMVar_hsa_circ_141977,RMVar_hsa_circ_141974 54379 RMVar_ID_54379 Human_SNP_ID_806992911 A-to-I Human chr10 + 21583049 21583049 21583049 AAAGTTAGCTGGACGTGGTGGCACACACCTGTAATTGCAGCTCCTTGGGAGGCTGAGGCAGGAGA AAAGTTAGCTGGACGTGGTGGCACACACCTGTGATTGCAGCTCCTTGGGAGGCTGAGGCAGGAGA A G MLLT10 Ensembl:ENSG00000078403 Protein coding intron GSE100210 HepG2 cell line chr10:21583049..21583050 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 5 prostate Human_RBP_ID_17558901 RMVar_hsa_circ_20632,RMVar_hsa_circ_22163,RMVar_hsa_circ_41652,RMVar_hsa_circ_119150,RMVar_hsa_circ_142578,RMVar_hsa_circ_97333,RMVar_hsa_circ_343303,RMVar_hsa_circ_361775,RMVar_hsa_circ_368909,RMVar_hsa_circ_349944,RMVar_hsa_circ_335552,RMVar_hsa_circ_60387,RMVar_hsa_circ_142579,RMVar_hsa_circ_142580,RMVar_hsa_circ_305967,RMVar_hsa_circ_332013,RMVar_hsa_circ_335012,RMVar_hsa_circ_58350,RMVar_hsa_circ_142581 54380 RMVar_ID_54380 Human_SNP_ID_807004335 A-to-I Human chr10 - 103390746 103390746 103390746 GACTCTTGTTGCCCAGGCTGGAGTGCAATGGCATGATCTTGGCTCACTGCAACCTCTGCCTCCCG GACTCTTGTTGCCCAGGCTGGAGTGCAATGGCGTGATCTTGGCTCACTGCAACCTCTGCCTCCCG T C ATP5MD Ensembl:ENSG00000173915 Protein coding intron GSE38233 cultured B-cells chr10:103390745..103390746 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_146065,RMVar_hsa_circ_119476,RMVar_hsa_circ_107147,RMVar_hsa_circ_146064 54381 RMVar_ID_54381 Human_SNP_ID_807033899 A-to-I Human chr10 + 41861506 41861506 41861506 GGAATGGAATGGACAGGAATGGAATGGAATGGAATGAAATCAACCCGATTGCAATGGAGTGGAAA GGAATGGAATGGACAGGAATGGAATGGAATGGTATGAAATCAACCCGATTGCAATGGAGTGGAAA A T - - Other Unknown GSE100210 HepG2 cell line chr10:41861506..41861507 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 3 - 54382 RMVar_ID_54382 Human_SNP_ID_807071082 A-to-I Human chr10 + 4979676 4979676 4979676 TAGGTCAGTCATTTGTAAATAGTACATCTGCTATGGACTTTTTCCAGTTCTTCACCATCCATTTT TAGGTCAGTCATTTGTAAATAGTACATCTGCTGTGGACTTTTTCCAGTTCTTCACCATCCATTTT A G AKR1C1 Ensembl:ENSG00000187134 Protein coding 3'UTR GSE100210 HepG2 cell line chr10:4979675..4979676 29129909 RNA-Seq:(High) rs797042714 Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_21881965 RMVar_hsa_circ_89943,RMVar_hsa_circ_141710 54383 RMVar_ID_54383 Human_SNP_ID_807074513 A-to-I Human chr10 + 102378506 102378506 102378506 AAAAATTATCTGGGCATGGTGGCACACATTGTAGTCCCAGCTACTGGGGAGGCTGAGTAGCTGAG AAAAATTATCTGGGCATGGTGGCACACATTGTGGTCCCAGCTACTGGGGAGGCTGAGTAGCTGAG A G GBF1 Ensembl:ENSG00000107862 Protein coding intron GSE38233 cultured B-cells chr10:102378505..102378506 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_12587,RMVar_hsa_circ_81558,RMVar_hsa_circ_145914,RMVar_hsa_circ_91871,RMVar_hsa_circ_101493,RMVar_hsa_circ_145926,RMVar_hsa_circ_145927,RMVar_hsa_circ_86398,RMVar_hsa_circ_369396,RMVar_hsa_circ_145934,RMVar_hsa_circ_145933 54384 RMVar_ID_54384 Human_SNP_ID_807095262 A-to-I Human chr10 + 73754977 73754977 73754977 GCAACATGGTGAAACCCTGTCTCTACCAAAATACTAAAATTAGCCGGGTGTGGTGGCACATGCCT GCAACATGGTGAAACCCTGTCTCTACCAAAATTCTAAAATTAGCCGGGTGTGGTGGCACATGCCT A T SEC24C Ensembl:ENSG00000176986 Protein coding intron GSE38233 cultured B-cells chr10:73754976..73754977 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_24833204 RMVar_hsa_circ_60050,RMVar_hsa_circ_126838,RMVar_hsa_circ_42416,RMVar_hsa_circ_144369 54385 RMVar_ID_54385 Human_SNP_ID_807153650 A-to-I Human chr10 + 103246303 103246303 103246303 CCTTTCATCTCGAGGCTACTGAGAACCCAGGGACTTTGATTAAAGACATTCGGGAGAATGGGATG CCTTTCATCTCGAGGCTACTGAGAACCCAGGGGCTTTGATTAAAGACATTCGGGAGAATGGGATG A G RPEL1 Ensembl:ENSG00000235376 Protein coding CDS GSE100210 HepG2 cell line chr10:103246302..103246303 29129909 RNA-Seq:(High) rs766118089 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,liver neoplasm,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 5 liver,haematopoietic and lymphoid tissue 54386 RMVar_ID_54386 Human_SNP_ID_807155308 A-to-I Human chr10 + 79351564 79351564 79351564 TACGGAAGCCGCTTTCCTGACGAGAACTTTACACTGAAGCACGTGGGGCCAGGTGAGTGGGGGCC TACGGAAGCCGCTTTCCTGACGAGAACTTTACCCTGAAGCACGTGGGGCCAGGTGAGTGGGGGCC A C PPIF Ensembl:ENSG00000108179 Protein coding exon GSE100210 HepG2 cell line chr10:79351563..79351564 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 thyroid neoplasm 1 head and neck Human_RBP_ID_383357,Human_RBP_ID_864316,Human_RBP_ID_984670,Human_RBP_ID_1450623,Human_RBP_ID_4143883,Human_RBP_ID_5162446,Human_RBP_ID_6005800,Human_RBP_ID_11440769,Human_RBP_ID_17344919,Human_RBP_ID_22432530,Human_RBP_ID_22752861 Human_Splice_Rec_1155004,Human_Splice_Rec_1155010,Human_Splice_Rec_1155020,Human_Splice_Rec_1155021,Human_Splice_Rec_1155034,Human_Splice_Rec_1155035 RMVar_hsa_circ_101125,RMVar_hsa_circ_144590 54387 RMVar_ID_54387 Human_SNP_ID_807177683 A-to-I Human chr10 - 92676319 92676319 92676319 AGTTCAGGCCAGGCATGGTGGCTGATGCCTGTAATCCCAGCAATTTGGGAGGCTGAAGCAGGAGG AGTTCAGGCCAGGCATGGTGGCTGATGCCTGTGATCCCAGCAATTTGGGAGGCTGAAGCAGGAGG T C lnc-IDE-3,lnc-IDE-3:2 RNACentral:URS0000D5AD79,RNACentral:URS0000D5871B lincRNA,lincRNA intron,exon GSE100210 HepG2 cell line chr10:92676318..92676319 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 54388 RMVar_ID_54388 Human_SNP_ID_807193193 A-to-I Human chr10 + 91942163 91942163 91942163 ACACTTAGCTAGGCATGGTTGTGTGCACCTGTAGTCCTAGCTACTCTGGAGGCTGAGGCAGAAGA ACACTTAGCTAGGCATGGTTGTGTGCACCTGTTGTCCTAGCTACTCTGGAGGCTGAGGCAGAAGA A T BTAF1 Ensembl:ENSG00000095564 Protein coding intron GSE100210 HepG2 cell line chr10:91942162..91942163 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_24397,RMVar_hsa_circ_300700,RMVar_hsa_circ_341436,RMVar_hsa_circ_69802,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_280293,RMVar_hsa_circ_51384,RMVar_hsa_circ_144905,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_144904 54389 RMVar_ID_54389 Human_SNP_ID_807252374 A-to-I Human chr10 - 103320818 103320818 103320818 GTGCATGGTTTACAGATATGTGACCTTCATTTATGGTTATTTACTAACAGGAACGAGTAATTCCC GTGCATGGTTTACAGATATGTGACCTTCATTTGTGGTTATTTACTAACAGGAACGAGTAATTCCC T C PCGF6 Ensembl:ENSG00000156374 Protein coding intron GSE38233 cultured B-cells chr10:103320817..103320818 24183664 RNA-Seq:(High) rs7093667 Functional Loss SNV ICGC 33..33 33 LAML 1 - GWAS_ID_2248,GWAS_ID_2249,GWAS_ID_2250,GWAS_ID_2251,GWAS_ID_2252,GWAS_ID_2253,GWAS_ID_2254,GWAS_ID_2255,GWAS_ID_2256,GWAS_ID_2257,GWAS_ID_2258,GWAS_ID_2259,GWAS_ID_2260,GWAS_ID_2261,GWAS_ID_2262,GWAS_ID_2263,GWAS_ID_2264,GWAS_ID_2265,GWAS_ID_2266,GWAS_ID_2267,GWAS_ID_2268,GWAS_ID_2269,GWAS_ID_2270,GWAS_ID_2271,GWAS_ID_2272,GWAS_ID_2273,GWAS_ID_2274,GWAS_ID_2275,GWAS_ID_2276,GWAS_ID_2277,GWAS_ID_2278,GWAS_ID_2279,GWAS_ID_2280,GWAS_ID_2281,GWAS_ID_2282 RMVar_hsa_circ_70813,RMVar_hsa_circ_96751,RMVar_hsa_circ_124980,RMVar_hsa_circ_112774,RMVar_hsa_circ_146039,RMVar_hsa_circ_146040,RMVar_hsa_circ_340038,RMVar_hsa_circ_370695,RMVar_hsa_circ_311081,RMVar_hsa_circ_88319,RMVar_hsa_circ_146041,RMVar_hsa_circ_146043,RMVar_hsa_circ_146044,RMVar_hsa_circ_146042 54390 RMVar_ID_54390 Human_SNP_ID_807301901 A-to-I Human chr10 + 12111269 12111269 12111269 CTCTCTGCAACCTCTGCCTCCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGG CTCTCTGCAACCTCTGCCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGG A G DHTKD1 Ensembl:ENSG00000181192 Protein coding intron GSE38233 cultured B-cells chr10:12111268..12111269 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - RMVar_hsa_circ_13286,RMVar_hsa_circ_312366,RMVar_hsa_circ_282118,RMVar_hsa_circ_272622,RMVar_hsa_circ_142087,RMVar_hsa_circ_142088,RMVar_hsa_circ_142086,RMVar_hsa_circ_358743,RMVar_hsa_circ_316042,RMVar_hsa_circ_142100,RMVar_hsa_circ_266206,RMVar_hsa_circ_290574,RMVar_hsa_circ_118851,RMVar_hsa_circ_142108,RMVar_hsa_circ_142109,RMVar_hsa_circ_373470,RMVar_hsa_circ_66717,RMVar_hsa_circ_142114,RMVar_hsa_circ_142115,RMVar_hsa_circ_367073,RMVar_hsa_circ_70661,RMVar_hsa_circ_142116,RMVar_hsa_circ_93028,RMVar_hsa_circ_115817,RMVar_hsa_circ_142117,RMVar_hsa_circ_335717,RMVar_hsa_circ_142121,RMVar_hsa_circ_142120,RMVar_hsa_circ_273375,RMVar_hsa_circ_142125,RMVar_hsa_circ_142126,RMVar_hsa_circ_357999,RMVar_hsa_circ_99155,RMVar_hsa_circ_104834,RMVar_hsa_circ_56050,RMVar_hsa_circ_324932,RMVar_hsa_circ_142128,RMVar_hsa_circ_142129,RMVar_hsa_circ_142127,RMVar_hsa_circ_372622,RMVar_hsa_circ_287548,RMVar_hsa_circ_142134,RMVar_hsa_circ_142133,RMVar_hsa_circ_113041,RMVar_hsa_circ_316140,RMVar_hsa_circ_360566,RMVar_hsa_circ_142139,RMVar_hsa_circ_96317,RMVar_hsa_circ_142136,RMVar_hsa_circ_142137,RMVar_hsa_circ_350651,RMVar_hsa_circ_316822,RMVar_hsa_circ_66117,RMVar_hsa_circ_142138 54391 RMVar_ID_54391 Human_SNP_ID_807312588 A-to-I Human chr10 + 115186581 115186581 115186581 CATTTGCACCATTGATGGAACTGGAAATCATTAAGTGAAATAAGCCAGGCACAGAAAGAAAACTG CATTTGCACCATTGATGGAACTGGAAATCATTCAGTGAAATAAGCCAGGCACAGAAAGAAAACTG A C ATRNL1 Ensembl:ENSG00000107518 Protein coding intron GSE107867 ASD brains,temporal_cortex chr10:115186580..115186581 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 2 liver RMVar_hsa_circ_291,RMVar_hsa_circ_274252,RMVar_hsa_circ_301732,RMVar_hsa_circ_305885,RMVar_hsa_circ_310668,RMVar_hsa_circ_302144,RMVar_hsa_circ_297166,RMVar_hsa_circ_300493,RMVar_hsa_circ_295486,RMVar_hsa_circ_280575,RMVar_hsa_circ_287569,RMVar_hsa_circ_289675,RMVar_hsa_circ_284040,RMVar_hsa_circ_279878,RMVar_hsa_circ_276037,RMVar_hsa_circ_46228,RMVar_hsa_circ_41238,RMVar_hsa_circ_33397,RMVar_hsa_circ_25270,RMVar_hsa_circ_297011,RMVar_hsa_circ_351820,RMVar_hsa_circ_360077,RMVar_hsa_circ_327538,RMVar_hsa_circ_311410,RMVar_hsa_circ_17098,RMVar_hsa_circ_36122,RMVar_hsa_circ_5472,RMVar_hsa_circ_41798,RMVar_hsa_circ_59916,RMVar_hsa_circ_274974,RMVar_hsa_circ_311565,RMVar_hsa_circ_34140,RMVar_hsa_circ_14678,RMVar_hsa_circ_24602,RMVar_hsa_circ_12792 54392 RMVar_ID_54392 Human_SNP_ID_807362576 A-to-I Human chr10 - 68030301 68030301 68030301 AAGTAGCTGGGATTATAGGCATGCACGATCACACCCGGCTATTTTTTGTATTTTTTTGTAGAGAT AAGTAGCTGGGATTATAGGCATGCACGATCACGCCCGGCTATTTTTTGTATTTTTTTGTAGAGAT T C HERC4 Ensembl:ENSG00000148634 Protein coding intron GSE100210 HepG2 cell line chr10:68030300..68030301 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_125199,RMVar_hsa_circ_143661,RMVar_hsa_circ_297679,RMVar_hsa_circ_275538,RMVar_hsa_circ_97971,RMVar_hsa_circ_108552,RMVar_hsa_circ_59326,RMVar_hsa_circ_143662,RMVar_hsa_circ_80660,RMVar_hsa_circ_113391,RMVar_hsa_circ_143672,RMVar_hsa_circ_320283,RMVar_hsa_circ_312802,RMVar_hsa_circ_277400,RMVar_hsa_circ_58500,RMVar_hsa_circ_73971,RMVar_hsa_circ_143675,RMVar_hsa_circ_143676,RMVar_hsa_circ_143673,RMVar_hsa_circ_143674,RMVar_hsa_circ_143687,RMVar_hsa_circ_72423,RMVar_hsa_circ_143682,RMVar_hsa_circ_318323,RMVar_hsa_circ_372966,RMVar_hsa_circ_280977,RMVar_hsa_circ_273519,RMVar_hsa_circ_143688,RMVar_hsa_circ_143700,RMVar_hsa_circ_45978,RMVar_hsa_circ_143685,RMVar_hsa_circ_143686,RMVar_hsa_circ_282075,RMVar_hsa_circ_143684,RMVar_hsa_circ_143695,RMVar_hsa_circ_334670,RMVar_hsa_circ_344718,RMVar_hsa_circ_49276,RMVar_hsa_circ_279414,RMVar_hsa_circ_143701,RMVar_hsa_circ_143702,RMVar_hsa_circ_143699,RMVar_hsa_circ_27343,RMVar_hsa_circ_315590,RMVar_hsa_circ_72407,RMVar_hsa_circ_294561,RMVar_hsa_circ_294472,RMVar_hsa_circ_50936,RMVar_hsa_circ_19229,RMVar_hsa_circ_143703,RMVar_hsa_circ_143704,RMVar_hsa_circ_317897,RMVar_hsa_circ_321834,RMVar_hsa_circ_143709,RMVar_hsa_circ_143711,RMVar_hsa_circ_319556,RMVar_hsa_circ_34458,RMVar_hsa_circ_50317,RMVar_hsa_circ_341745,RMVar_hsa_circ_365812,RMVar_hsa_circ_271218,RMVar_hsa_circ_279810,RMVar_hsa_circ_20291,RMVar_hsa_circ_113913,RMVar_hsa_circ_311037,RMVar_hsa_circ_378339,RMVar_hsa_circ_143710,RMVar_hsa_circ_346845,RMVar_hsa_circ_272171,RMVar_hsa_circ_143714,RMVar_hsa_circ_3277,RMVar_hsa_circ_143715,RMVar_hsa_circ_143713 54393 RMVar_ID_54393 Human_SNP_ID_807363315 A-to-I Human chr10 - 32290763 32290763 32290763 CTAAAAAAAAAAAGATAAAAAAAGAAAAATACATATATACCCCACCTTAATGTATACTGCAATGA CTAAAAAAAAAAAGATAAAAAAAGAAAAATACGTATATACCCCACCTTAATGTATACTGCAATGA T C EPC1 Ensembl:ENSG00000120616 Protein coding intron GSE38233 cultured B-cells chr10:32290762..32290763 24183664 RNA-Seq:(High) rs3006623 Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_85336,RMVar_hsa_circ_143021,RMVar_hsa_circ_143024,RMVar_hsa_circ_80823,RMVar_hsa_circ_143023,RMVar_hsa_circ_45266,RMVar_hsa_circ_143027,RMVar_hsa_circ_307506,RMVar_hsa_circ_27870 54394 RMVar_ID_54394 Human_SNP_ID_807379017 A-to-I Human chr10 - 73116284 73116284 73116284 ATTTCTTAGGCTGGGCATGGTGGCTCATGCCTATAATCCCAGCACTTTGGGAGGTAAAGGCAGGA ATTTCTTAGGCTGGGCATGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGTAAAGGCAGGA T C - - Other Unknown GSE100210 HepG2 cell line chr10:73116283..73116284 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - 54395 RMVar_ID_54395 Human_SNP_ID_807464276 A-to-I Human chr10 + 5719482 5719482 5719482 TTCCTACCTCAGCCTCCCAAGTGGCTGGGACTACAGGCGCGCGCTACCACACCCAGCTAATTTTT TTCCTACCTCAGCCTCCCAAGTGGCTGGGACTGCAGGCGCGCGCTACCACACCCAGCTAATTTTT A G TASOR2 Ensembl:ENSG00000108021 Protein coding intron GSE100210 HepG2 cell line chr10:5719481..5719482 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_11375278 RMVar_hsa_circ_1150,RMVar_hsa_circ_93748,RMVar_hsa_circ_141742,RMVar_hsa_circ_141739,RMVar_hsa_circ_141744,RMVar_hsa_circ_141743,RMVar_hsa_circ_26688,RMVar_hsa_circ_141750,RMVar_hsa_circ_347871,RMVar_hsa_circ_367579,RMVar_hsa_circ_72515,RMVar_hsa_circ_104317,RMVar_hsa_circ_30246,RMVar_hsa_circ_338248,RMVar_hsa_circ_327032,RMVar_hsa_circ_349601,RMVar_hsa_circ_370345,RMVar_hsa_circ_334878,RMVar_hsa_circ_105337,RMVar_hsa_circ_92584,RMVar_hsa_circ_104124,RMVar_hsa_circ_72308,RMVar_hsa_circ_141752,RMVar_hsa_circ_141754,RMVar_hsa_circ_141755,RMVar_hsa_circ_141756,RMVar_hsa_circ_141753,RMVar_hsa_circ_141751 54396 RMVar_ID_54396 Human_SNP_ID_807475212 A-to-I Human chr10 + 86773409 86773409 86773409 TCAGGAGTTTGAGACTAGCCTAGCTAACATATAGTGGAACCCTGTCTCTACTAAAAAAGTACAAA TCAGGAGTTTGAGACTAGCCTAGCTAACATATGGTGGAACCCTGTCTCTACTAAAAAAGTACAAA A G BMPR1A Ensembl:ENSG00000107779 Protein coding intron GSE100210 HepG2 cell line chr10:86773408..86773409 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - RMVar_hsa_circ_110474,RMVar_hsa_circ_127063,RMVar_hsa_circ_144708,RMVar_hsa_circ_144709 54397 RMVar_ID_54397 Human_SNP_ID_807480697 A-to-I Human chr10 - 6283550 6283550 6283550 GCTCTTTCCTCTCATTCAGGGCTGAGTCTTCCAGCCTCCATCTTTCTCCCATGCTGGATGCTTCC GCTCTTTCCTCTCATTCAGGGCTGAGTCTTCCGGCCTCCATCTTTCTCCCATGCTGGATGCTTCC T C - - Other Unknown GSE38233 cultured B-cells chr10:6283549..6283550 24183664 RNA-Seq:(High) rs5027484 Functional Loss SNV ICGC 33..33 33 COCA 1 - 54398 RMVar_ID_54398 Human_SNP_ID_807487214 A-to-I Human chr10 + 99796448 99796448 99796448 ATCGCTTGAACCTGGGAGGCAGATCTTGCAGTAAGCCGAGGTCGCGCCACTGCACTCCAGCCTAT ATCGCTTGAACCTGGGAGGCAGATCTTGCAGTTAGCCGAGGTCGCGCCACTGCACTCCAGCCTAT A T ABCC2 Ensembl:ENSG00000023839 Protein coding intron GSE100210 HepG2 cell line chr10:99796447..99796448 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_24542118 Human_Splice_Rec_1167666,Human_Splice_Rec_1167708 RMVar_hsa_circ_112634,RMVar_hsa_circ_118260,RMVar_hsa_circ_11062,RMVar_hsa_circ_107979,RMVar_hsa_circ_145525,RMVar_hsa_circ_145526,RMVar_hsa_circ_127932,RMVar_hsa_circ_95581,RMVar_hsa_circ_84578,RMVar_hsa_circ_145528,RMVar_hsa_circ_145529,RMVar_hsa_circ_145527,RMVar_hsa_circ_145532,RMVar_hsa_circ_95147,RMVar_hsa_circ_58476,RMVar_hsa_circ_114491,RMVar_hsa_circ_124552,RMVar_hsa_circ_145533,RMVar_hsa_circ_115800,RMVar_hsa_circ_110300,RMVar_hsa_circ_79121,RMVar_hsa_circ_145537,RMVar_hsa_circ_145539,RMVar_hsa_circ_145540,RMVar_hsa_circ_145538,RMVar_hsa_circ_145536,RMVar_hsa_circ_145541,RMVar_hsa_circ_113090 54399 RMVar_ID_54399 Human_SNP_ID_807510552 A-to-I Human chr10 + 122384691 122384691 122384691 AAATTGTTACTGCTCCAGGTGTGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAATGC AAATTGTTACTGCTCCAGGTGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAATGC A G PLEKHA1 Ensembl:ENSG00000107679 Protein coding intron GSE100210 HepG2 cell line chr10:122384690..122384691 29129909 RNA-Seq:(High) rs1362830563 Functional Loss SNV ICGC 33..33 33 ESCA 1 - 54400 RMVar_ID_54400 Human_SNP_ID_807554581 A-to-I Human chr10 + 68759230 68759230 68759230 CAGTCTAGGAGTTTGAGATCAGCTTCTGCAACATAGTGAGGCCCTGTCTCTACAAAAAGTTTAAA CAGTCTAGGAGTTTGAGATCAGCTTCTGCAACGTAGTGAGGCCCTGTCTCTACAAAAAGTTTAAA A G CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr10:68759229..68759230 24183664,29129909 RNA-Seq:(High) rs1183146757 Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_22883697,Human_RBP_ID_23464579 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_52772,RMVar_hsa_circ_308624 54401 RMVar_ID_54401 Human_SNP_ID_807571574 A-to-I Human chr10 + 72755892 72755892 72755892 AGACAGAGTCTCTCTCTCTGTTACCCAGGCTTAGAGTGCAGTGATATGATCATAGCTCACTGCAG AGACAGAGTCTCTCTCTCTGTTACCCAGGCTTCGAGTGCAGTGATATGATCATAGCTCACTGCAG A C MCU Ensembl:ENSG00000156026 Protein coding intron GSE100210 HepG2 cell line chr10:72755891..72755892 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - RMVar_hsa_circ_308267,RMVar_hsa_circ_305538,RMVar_hsa_circ_108317,RMVar_hsa_circ_144203,RMVar_hsa_circ_311083,RMVar_hsa_circ_144202 54402 RMVar_ID_54402 Human_SNP_ID_807578319 A-to-I Human chr10 - 86947977 86947977 86947977 CTCCCACCTCAGCCTCCCAAAGTGCTGGGGTTACAGGCGTGCGCCACTGTACCTGGCCCTCTTTT CTCCCACCTCAGCCTCCCAAAGTGCTGGGGTTGCAGGCGTGCGCCACTGTACCTGGCCCTCTTTT T C MMRN2 Ensembl:ENSG00000173269 Protein coding intron GSE100210 HepG2 cell line chr10:86947976..86947977 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 COCA 1 - 54403 RMVar_ID_54403 Human_SNP_ID_807618423 A-to-I Human chr10 + 68770160 68770160 68770160 ATGTCACCTTATCAGAGAGGCCTTGTCTTACTATTCTCTCTTGTTATACTCTAGGTGTTTATCCT ATGTCACCTTATCAGAGAGGCCTTGTCTTACTGTTCTCTCTTGTTATACTCTAGGTGTTTATCCT A G CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE38233 cultured B-cells chr10:68770159..68770160 24183664 RNA-Seq:(High) rs9415936 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_5991069,Human_RBP_ID_19536327 GWAS_ID_2044,GWAS_ID_2045,GWAS_ID_2046,GWAS_ID_2047,GWAS_ID_2048,GWAS_ID_2049,GWAS_ID_2050,GWAS_ID_2051,GWAS_ID_2052,GWAS_ID_2053,GWAS_ID_2054,GWAS_ID_2055,GWAS_ID_2056,GWAS_ID_2057,GWAS_ID_2058,GWAS_ID_2059,GWAS_ID_2060,GWAS_ID_2061,GWAS_ID_2062,GWAS_ID_2063,GWAS_ID_2064,GWAS_ID_2065,GWAS_ID_2066,GWAS_ID_2067,GWAS_ID_2068,GWAS_ID_2069,GWAS_ID_2070,GWAS_ID_2071,GWAS_ID_2072 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_143910,RMVar_hsa_circ_27926 54404 RMVar_ID_54404 Human_SNP_ID_807647067 A-to-I Human chr10 - 60410804 60410804 60410804 AAAATTGGCCAGGCATTCTGGTGTGCACCTGTAGTCCCAGCTACTCAGGATGCTAAGACAGGAGG AAAATTGGCCAGGCATTCTGGTGTGCACCTGTTGTCCCAGCTACTCAGGATGCTAAGACAGGAGG T A ANK3 Ensembl:ENSG00000151150 Protein coding intron GSE107867 ASD brains,temporal_cortex chr10:60410803..60410804 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 3 liver 54405 RMVar_ID_54405 Human_SNP_ID_807652426 A-to-I Human chr10 + 102927504 102927504 102927504 GCAGTTGGCTGGGCGTGGTGGCTCATGCCTGTAATCCCGGCACTTTGGGAGGCCCAGGGAGGTGG GCAGTTGGCTGGGCGTGGTGGCTCATGCCTGTCATCCCGGCACTTTGGGAGGCCCAGGGAGGTGG A C CNNM2 Ensembl:ENSG00000148842 Protein coding intron GSE100210 HepG2 cell line chr10:102927503..102927504 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 5 lung Human_RBP_ID_11246947 54406 RMVar_ID_54406 Human_SNP_ID_807667055 A-to-I Human chr10 - 119163878 119163878 119163878 GCGCCACCATGCCCGGCTAATTTTGTATTTTTAGTAGAGACGGGGGTTTCTCCATGTTGGTCAGG GCGCCACCATGCCCGGCTAATTTTGTATTTTTGGTAGAGACGGGGGTTTCTCCATGTTGGTCAGG T C SFXN4 Ensembl:ENSG00000183605 Protein coding intron GSE38233 cultured B-cells chr10:119163877..119163878 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_13049,RMVar_hsa_circ_83195,RMVar_hsa_circ_49112,RMVar_hsa_circ_269372,RMVar_hsa_circ_146661 54407 RMVar_ID_54407 Human_SNP_ID_807724701 A-to-I Human chr10 + 42820931 42820931 42820931 GTTCGCTATATTTCTTTTTTTCCTTTTCCTTTAAGGCCCTATCACTCCACAGGGAACTGGTTTCT GTTCGCTATATTTCTTTTTTTCCTTTTCCTTTTAGGCCCTATCACTCCACAGGGAACTGGTTTCT A T BMS1 Ensembl:ENSG00000165733 Protein coding intron GSE105773 Glioblastoma cells,U87MG chr10:42820931..42820932 29724793 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung adenocarcinoma,LUAD 3 lung Human_RBP_ID_861159,Human_RBP_ID_5339876,Human_RBP_ID_5971853,Human_RBP_ID_8334535,Human_RBP_ID_19517313,Human_RBP_ID_24556753,Human_RBP_ID_24811945 Human_Splice_Rec_1127237 RMVar_hsa_circ_638,RMVar_hsa_circ_143231,RMVar_hsa_circ_79134,RMVar_hsa_circ_83573,RMVar_hsa_circ_85213,RMVar_hsa_circ_143234,RMVar_hsa_circ_143235,RMVar_hsa_circ_70322,RMVar_hsa_circ_334722,RMVar_hsa_circ_143243,RMVar_hsa_circ_268143 54408 RMVar_ID_54408 Human_SNP_ID_807731695 A-to-I Human chr10 - 42628311 42628311 42628311 AGCATCATTATAGAATAGTGCTCAACAAGGCCAGGTGCGGTGTCTCACGCCTGTAATTCCAGCAC AGCATCATTATAGAATAGTGCTCAACAAGGCCGGGTGCGGTGTCTCACGCCTGTAATTCCAGCAC T C ZNF33B Ensembl:ENSG00000196693 Protein coding intron GSE100210 HepG2 cell line chr10:42628310..42628311 29129909 RNA-Seq:(High) rs371796352 Functional Loss SNV ICGC 33..33 33 LMS 1 - Human_RBP_ID_22565826 RMVar_hsa_circ_38549,RMVar_hsa_circ_56025,RMVar_hsa_circ_52373 54409 RMVar_ID_54409 Human_SNP_ID_807752939 A-to-I Human chr10 - 34111190 34111190 34111190 GCGAGGCTGAACAGACTTCAGACTCCTGAGAAAGGGAGGCCCTTCTATTCCTGAGCACGCAAATA GCGAGGCTGAACAGACTTCAGACTCCTGAGAACGGGAGGCCCTTCTATTCCTGAGCACGCAAATA T G PARD3 Ensembl:ENSG00000148498 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector chr10:34111189..34111190 29967493 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_17776560 RMVar_hsa_circ_110908,RMVar_hsa_circ_118270,RMVar_hsa_circ_143102,RMVar_hsa_circ_101575,RMVar_hsa_circ_143103,RMVar_hsa_circ_143101 54410 RMVar_ID_54410 Human_SNP_ID_807768095 A-to-I Human chr10 - 119074771 119074771 119074771 GCACCACTACGCCCTGCTAATTTTGTATTTTTAGTAGAGACTTGGTTTCTCCATTTTGGTTAGGC GCACCACTACGCCCTGCTAATTTTGTATTTTTGGTAGAGACTTGGTTTCTCCATTTTGGTTAGGC T C EIF3A Ensembl:ENSG00000107581 Protein coding intron GSE38233 cultured B-cells chr10:119074770..119074771 24183664 RNA-Seq:(High) rs1453488162 Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ER-HER-positive_carcinoma,breast HER-positive_carcinoma 5 breast RMVar_hsa_circ_117679,RMVar_hsa_circ_146630 54411 RMVar_ID_54411 Human_SNP_ID_807778469 A-to-I Human chr10 + 87097552 87097552 87097552 GGAGAGAGGTTGCAGTGAGCCGAGATCGTGCCATTGCACTCCAGCCTGGGCAACAGAGCGAGTCT GGAGAGAGGTTGCAGTGAGCCGAGATCGTGCCGTTGCACTCCAGCCTGGGCAACAGAGCGAGTCT A G SHLD2 Ensembl:ENSG00000122376 Protein coding intron GSE38233 cultured B-cells chr10:87097551..87097552 24183664 RNA-Seq:(High) rs1358819773 Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_17559109,Human_RBP_ID_22708583,Human_RBP_ID_26775334 RMVar_hsa_circ_7600,RMVar_hsa_circ_107189,RMVar_hsa_circ_376242,RMVar_hsa_circ_144742,RMVar_hsa_circ_348612,RMVar_hsa_circ_144743 54412 RMVar_ID_54412 Human_SNP_ID_807784340 A-to-I Human chr10 - 103136789 103136789 103136789 AAACCCCATCTCTACTAAAAAATACAAAAATTAGTTGGGTGTGGTGGTACGTGCCTGTAGTCTCA AAACCCCATCTCTACTAAAAAATACAAAAATTGGTTGGGTGTGGTGGTACGTGCCTGTAGTCTCA T C NT5C2 Ensembl:ENSG00000076685 Protein coding intron GSE100210 HepG2 cell line chr10:103136788..103136789 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_2187420 RMVar_hsa_circ_109953,RMVar_hsa_circ_146021,RMVar_hsa_circ_26858,RMVar_hsa_circ_64491,RMVar_hsa_circ_343970,RMVar_hsa_circ_146029,RMVar_hsa_circ_146031,RMVar_hsa_circ_87429,RMVar_hsa_circ_316578,RMVar_hsa_circ_146030,RMVar_hsa_circ_335269,RMVar_hsa_circ_319725,RMVar_hsa_circ_323188,RMVar_hsa_circ_322332 54413 RMVar_ID_54413 Human_SNP_ID_807787191 A-to-I Human chr10 + 68792923 68792923 68792923 CCCCTGCCTTAGCCTCTCAAGTAGCTGGGATTACAGACGTCTGCCACCATGTTCAGCTAATTTTG CCCCTGCCTTAGCCTCTCAAGTAGCTGGGATTGCAGACGTCTGCCACCATGTTCAGCTAATTTTG A G - - Other Unknown GSE100210 HepG2 cell line chr10:68792922..68792923 29129909 RNA-Seq:(High) rs896389932 Functional Loss SNV ICGC 33..33 33 MELA 1 - 54414 RMVar_ID_54414 Human_SNP_ID_807789745 A-to-I Human chr10 - 17615845 17615845 17615845 CTCCTGCCTCGGCCTCCGGAGTAGCTGGGACTACAAGCGTGGGCCACCACGCCCCATTAATTTTT CTCCTGCCTCGGCCTCCGGAGTAGCTGGGACTGCAAGCGTGGGCCACCACGCCCCATTAATTTTT T C HACD1 Ensembl:ENSG00000165996 Protein coding intron GSE100210 HepG2 cell line chr10:17615844..17615845 29129909 RNA-Seq:(High) rs1420980702 Functional Loss SNV ICGC 33..33 33 LUSC 1 - RMVar_hsa_circ_115426,RMVar_hsa_circ_142467 54415 RMVar_ID_54415 Human_SNP_ID_807818224 A-to-I Human chr10 + 84437455 84437455 84437455 AGAATCGCTTGAACTCCGGAGGCAGAGGTTACAATGAGCCAAGATCGTACCATTGCGCTCCAGCC AGAATCGCTTGAACTCCGGAGGCAGAGGTTACGATGAGCCAAGATCGTACCATTGCGCTCCAGCC A G CCSER2 Ensembl:ENSG00000107771 Protein coding intron GSE100210 HepG2 cell line chr10:84437455..84437456 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 CLLE 1 - RMVar_hsa_circ_144656,RMVar_hsa_circ_361919,RMVar_hsa_circ_93302,RMVar_hsa_circ_144655,RMVar_hsa_circ_5225,RMVar_hsa_circ_272301,RMVar_hsa_circ_314219,RMVar_hsa_circ_275434,RMVar_hsa_circ_23828,RMVar_hsa_circ_144664,RMVar_hsa_circ_144665,RMVar_hsa_circ_144663,RMVar_hsa_circ_282960,RMVar_hsa_circ_57924,RMVar_hsa_circ_144667,RMVar_hsa_circ_144668 54416 RMVar_ID_54416 Human_SNP_ID_807895111 A-to-I Human chr10 - 18654639 18654639 18654639 TGACTTGGTGATCCACCCGCCTCAGCCTCCCAAAGTGTTGGGATTACAGGCATGAGCCACTGCGC TGACTTGGTGATCCACCCGCCTCAGCCTCCCACAGTGTTGGGATTACAGGCATGAGCCACTGCGC T G NSUN6 Ensembl:ENSG00000241058 Protein coding intron GSE100210 HepG2 cell line chr10:18654638..18654639 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_53695,RMVar_hsa_circ_291385,RMVar_hsa_circ_142505,RMVar_hsa_circ_350759,RMVar_hsa_circ_341950,RMVar_hsa_circ_360438,RMVar_hsa_circ_366855,RMVar_hsa_circ_312870 54417 RMVar_ID_54417 Human_SNP_ID_808047345 A-to-I Human chr10 - 7352383 7352383 7352383 AGGAGGTCGAGGCTGCAGTGAGCTGTGATTGCACCACTGTACTCCCACCTGGGTGACAGAGTGAG AGGAGGTCGAGGCTGCAGTGAGCTGTGATTGCTCCACTGTACTCCCACCTGGGTGACAGAGTGAG T A SFMBT2 Ensembl:ENSG00000198879 Protein coding intron GSE100210 HepG2 cell line chr10:7352382..7352383 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_11415959,Human_RBP_ID_24860482 RMVar_hsa_circ_15750,RMVar_hsa_circ_317668,RMVar_hsa_circ_58187,RMVar_hsa_circ_2807,RMVar_hsa_circ_126640,RMVar_hsa_circ_361628,RMVar_hsa_circ_141842,RMVar_hsa_circ_141843,RMVar_hsa_circ_328246,RMVar_hsa_circ_104180,RMVar_hsa_circ_329598,RMVar_hsa_circ_141858,RMVar_hsa_circ_94735,RMVar_hsa_circ_353940,RMVar_hsa_circ_287262,RMVar_hsa_circ_128049,RMVar_hsa_circ_141863,RMVar_hsa_circ_141865,RMVar_hsa_circ_72660,RMVar_hsa_circ_141866,RMVar_hsa_circ_141864,RMVar_hsa_circ_63393,RMVar_hsa_circ_114208,RMVar_hsa_circ_75379,RMVar_hsa_circ_141869,RMVar_hsa_circ_141870 54418 RMVar_ID_54418 Human_SNP_ID_808087877 A-to-I Human chr10 + 133207181 133207181 133207181 GAACGCTGGGGCCTGGAGCCCTGCACCCTCCCAGTGATCGTGAACATCGCGGCCGCACCCTGCGA GAACGCTGGGGCCTGGAGCCCTGCACCCTCCCGGTGATCGTGAACATCGCGGCCGCACCCTGCGA A G KNDC1 Ensembl:ENSG00000171798 Protein coding CDS GSE47997 K562 cells&HepG2 cells chr10:133207180..133207181 23474544 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 2 large intestine RMVar_hsa_circ_103909,RMVar_hsa_circ_120446,RMVar_hsa_circ_147291,RMVar_hsa_circ_88527,RMVar_hsa_circ_147292,RMVar_hsa_circ_127766,RMVar_hsa_circ_147293,RMVar_hsa_circ_147294 54419 RMVar_ID_54419 Human_SNP_ID_808299707 A-to-I Human chr10 - 75382557 75382557 75382557 AACAAGAAAACTCTCCAATATCTGGGAAGGAGAAAGAGACACCAGTCACCATCTTAGACTCTTCT AACAAGAAAACTCTCCAATATCTGGGAAGGAGGAAGAGACACCAGTCACCATCTTAGACTCTTCT T C AC010997.3,SPA17P1 Ensembl:ENSG00000270087,Ensembl:ENSG00000236797 lincRNA,Pseudogene intron,exon GSE100210 HepG2 cell line chr10:75382556..75382557 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 1 - 54420 RMVar_ID_54420 Human_SNP_ID_808393241 A-to-I Human chr10 - 18594652 18594652 18594652 GAGGTTAAGAGATCGAGACCATCCAGGCCAACATGTGAAACCCCATCTCTACTAAAAATACAAAA GAGGTTAAGAGATCGAGACCATCCAGGCCAACCTGTGAAACCCCATCTCTACTAAAAATACAAAA T G NSUN6 Ensembl:ENSG00000241058 Protein coding intron GSE100210 HepG2 cell line chr10:18594651..18594652 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 2 breast 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 54421 RMVar_ID_54421 Human_SNP_ID_808446897 A-to-I Human chr10 + 68759278 68759278 68759278 TCTACAAAAAGTTTAAAAAATTATTTGGGCATAGTGGCACACGCCTGTAGTCCCAGCTACTTGGG TCTACAAAAAGTTTAAAAAATTATTTGGGCATGGTGGCACACGCCTGTAGTCCCAGCTACTTGGG A G CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BERP35T1 cell line chr10:68759277..68759278 24183664,29129909,31158229 RNA-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_17559304,Human_RBP_ID_24860034 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_52772,RMVar_hsa_circ_308624 54422 RMVar_ID_54422 Human_SNP_ID_808501004 A-to-I Human chr10 - 70163953 70163953 70163953 AATATAGCCATTGCCATCCTTATCAAACACACAGAATGTTTCTCTAATTTCTTCTTCACTGTCTG AATATAGCCATTGCCATCCTTATCAAACACACGGAATGTTTCTCTAATTTCTTCTTCACTGTCTG T C SAR1A Ensembl:ENSG00000079332 Protein coding intron GSE100210 HepG2 cell line chr10:70163952..70163953 29129909 RNA-Seq:(High) rs879030462 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 haematopoietic and lymphoid tissue Human_RBP_ID_3355555 RMVar_hsa_circ_105466,RMVar_hsa_circ_144047 54423 RMVar_ID_54423 Human_SNP_ID_808508033 A-to-I Human chr10 - 95388193 95388193 95388193 GGTGGATCACCTGCGGTCAGGAGTTCGAGACCAGCTTGACAAATATGGTGAAACCCCATCTCTAC GGTGGATCACCTGCGGTCAGGAGTTCGAGACCTGCTTGACAAATATGGTGAAACCCCATCTCTAC T A SORBS1 Ensembl:ENSG00000095637 Protein coding intron GSE107867 ASD brains,temporal_cortex chr10:95388192..95388193 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_295121,RMVar_hsa_circ_67586,RMVar_hsa_circ_62526,RMVar_hsa_circ_145243,RMVar_hsa_circ_69240,RMVar_hsa_circ_363185,RMVar_hsa_circ_105463,RMVar_hsa_circ_65678,RMVar_hsa_circ_30997,RMVar_hsa_circ_145250,RMVar_hsa_circ_330916,RMVar_hsa_circ_145252,RMVar_hsa_circ_325722,RMVar_hsa_circ_145254,RMVar_hsa_circ_145253,RMVar_hsa_circ_324732,RMVar_hsa_circ_267072,RMVar_hsa_circ_359047,RMVar_hsa_circ_282590,RMVar_hsa_circ_61985,RMVar_hsa_circ_145257,RMVar_hsa_circ_24493,RMVar_hsa_circ_145256 54424 RMVar_ID_54424 Human_SNP_ID_808550682 A-to-I Human chr10 + 124538176 124538176 124538176 CATGCAGGGTCACCACGCGAGTCTCACCATGCAGGGTCACCATGCGGGGTCACCATGTGGGGTCA CATGCAGGGTCACCACGCGAGTCTCACCATGCGGGGTCACCATGCGGGGTCACCATGTGGGGTCA A G LHPP Ensembl:ENSG00000107902 Protein coding intron GSE100210 HepG2 cell line chr10:124538175..124538176 29129909 RNA-Seq:(High) rs72837318 Functional Loss SNV ICGC,COSMIC 33..33 33 prostate adenocarcinoma,STAD 3 prostate RMVar_hsa_circ_102074,RMVar_hsa_circ_146937,RMVar_hsa_circ_86169,RMVar_hsa_circ_113672,RMVar_hsa_circ_146946,RMVar_hsa_circ_146947 54425 RMVar_ID_54425 Human_SNP_ID_808589152 A-to-I Human chr10 - 86491016 86491016 86491016 CTCTGTCACCCAGGCTGGAGTGCGGTGGCATGATCTCGGCTCACTGCAACCTCCGCCTCCTGGGT CTCTGTCACCCAGGCTGGAGTGCGGTGGCATGTTCTCGGCTCACTGCAACCTCCGCCTCCTGGGT T A WAPL Ensembl:ENSG00000062650 Protein coding intron GSE100210 HepG2 cell line chr10:86491015..86491016 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_37954,RMVar_hsa_circ_267851,RMVar_hsa_circ_55062,RMVar_hsa_circ_352490,RMVar_hsa_circ_70741,RMVar_hsa_circ_72754,RMVar_hsa_circ_51925,RMVar_hsa_circ_356921,RMVar_hsa_circ_358268,RMVar_hsa_circ_62216,RMVar_hsa_circ_43209,RMVar_hsa_circ_92276,RMVar_hsa_circ_352846,RMVar_hsa_circ_52597,RMVar_hsa_circ_332986,RMVar_hsa_circ_144706,RMVar_hsa_circ_61157,RMVar_hsa_circ_144707,RMVar_hsa_circ_367231 54426 RMVar_ID_54426 Human_SNP_ID_808606372 A-to-I Human chr10 - 43789704 43789704 43789704 GGTGGATCTGGCAATTGTATGGGTCACAGAGGAAACTTTGGAGGTGGTGGAGGTAATTTTGGCCG GGTGGATCTGGCAATTGTATGGGTCACAGAGGCAACTTTGGAGGTGGTGGAGGTAATTTTGGCCG T G HNRNPA3P1 Ensembl:ENSG00000226790 Pseudogene exon GSE100210 HepG2 cell line chr10:43789703..43789704 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA 33..33 33 SKCM 1 - 54427 RMVar_ID_54427 Human_SNP_ID_808636699 A-to-I Human chr10 - 68429379 68429379 68429379 TGACCACGTCCTGCTAATTTCGTATTTTTAGTAGAGACAGGGTTTCTCCGTGTTGGTCAGGCTGG TGACCACGTCCTGCTAATTTCGTATTTTTAGTTGAGACAGGGTTTCTCCGTGTTGGTCAGGCTGG T A DNA2 Ensembl:ENSG00000138346 Protein coding intron GSE38233 cultured B-cells chr10:68429378..68429379 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_11398224 RMVar_hsa_circ_1990,RMVar_hsa_circ_3370,RMVar_hsa_circ_81122,RMVar_hsa_circ_331452,RMVar_hsa_circ_269327,RMVar_hsa_circ_143780,RMVar_hsa_circ_370626,RMVar_hsa_circ_278117,RMVar_hsa_circ_29376,RMVar_hsa_circ_143782,RMVar_hsa_circ_143783,RMVar_hsa_circ_143784,RMVar_hsa_circ_371591,RMVar_hsa_circ_24880,RMVar_hsa_circ_143786,RMVar_hsa_circ_143785,RMVar_hsa_circ_325058,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_5242,RMVar_hsa_circ_121562,RMVar_hsa_circ_143792,RMVar_hsa_circ_143793,RMVar_hsa_circ_143794 54428 RMVar_ID_54428 Human_SNP_ID_808661803 A-to-I Human chr10 + 91845823 91845823 91845823 TGTGTCAATGCCACGGACAAATGGGCTTTCACACCTTTGCACGAAGCAGCCCAAAAGGGACGAAC TGTGTCAATGCCACGGACAAATGGGCTTTCACGCCTTTGCACGAAGCAGCCCAAAAGGGACGAAC A G TNKS2 Ensembl:ENSG00000107854 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr10:91845822..91845823 30559470 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 3 large intestine Human_RBP_ID_1772621,Human_RBP_ID_8764119,Human_RBP_ID_11458259,Human_RBP_ID_18600171 Human_Splice_Rec_1159728 Human_miRNA_ID_2180864,Human_miRNA_ID_2182968,Human_miRNA_ID_2794364,Human_miRNA_ID_2794830,Human_miRNA_ID_2795297 RMVar_hsa_circ_144867,RMVar_hsa_circ_124373,RMVar_hsa_circ_115081,RMVar_hsa_circ_144870,RMVar_hsa_circ_324445,RMVar_hsa_circ_50300,RMVar_hsa_circ_4305,RMVar_hsa_circ_21842,RMVar_hsa_circ_33200,RMVar_hsa_circ_9731,RMVar_hsa_circ_102214,RMVar_hsa_circ_370767,RMVar_hsa_circ_144878,RMVar_hsa_circ_144879,RMVar_hsa_circ_320391,RMVar_hsa_circ_346866,RMVar_hsa_circ_144885,RMVar_hsa_circ_144886,RMVar_hsa_circ_144891,RMVar_hsa_circ_343015,RMVar_hsa_circ_353329,RMVar_hsa_circ_308328,RMVar_hsa_circ_285168,RMVar_hsa_circ_35648,RMVar_hsa_circ_19573,RMVar_hsa_circ_144895,RMVar_hsa_circ_144896,RMVar_hsa_circ_69408 54429 RMVar_ID_54429 Human_SNP_ID_808723251 A-to-I Human chr10 - 4994226 4994226 4994226 TCATATATTCTCAAGAATTCATACAAGTCTCTAAAGAATTAACATCCAGAATACATACATATGTG TCATATATTCTCAAGAATTCATACAAGTCTCTGAAGAATTAACATCCAGAATACATACATATGTG T C AKR1C2 Ensembl:ENSG00000151632 Protein coding intron GSE100210 HepG2 cell line chr10:4994225..4994226 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 3 breast RMVar_hsa_circ_69713,RMVar_hsa_circ_362486,RMVar_hsa_circ_65022 54430 RMVar_ID_54430 Human_SNP_ID_808736856 A-to-I Human chr10 - 103117587 103117587 103117587 GCTGCAGCACAGTGGTGCAATTGTAGTTTACTATAACCTTGAACTACTGGGCTCAAGTGATCCTC GCTGCAGCACAGTGGTGCAATTGTAGTTTACTGTAACCTTGAACTACTGGGCTCAAGTGATCCTC T C NT5C2 Ensembl:ENSG00000076685 Protein coding intron GSE100210 HepG2 cell line chr10:103117586..103117587 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_109953,RMVar_hsa_circ_146021,RMVar_hsa_circ_26858,RMVar_hsa_circ_64491,RMVar_hsa_circ_343970,RMVar_hsa_circ_146029,RMVar_hsa_circ_146031,RMVar_hsa_circ_87429,RMVar_hsa_circ_316578,RMVar_hsa_circ_146030,RMVar_hsa_circ_335269,RMVar_hsa_circ_323188 54431 RMVar_ID_54431 Human_SNP_ID_808807822 A-to-I Human chr10 + 101364958 101364958 101364958 TGCTCCAAAAATCTATTTAATATATTGTCCTCAGATAGAGGACATATCAGATACTAAACTGATGA TGCTCCAAAAATCTATTTAATATATTGTCCTCGGATAGAGGACATATCAGATACTAAACTGATGA A G BTRC Ensembl:ENSG00000166167 Protein coding intron GSE100210 HepG2 cell line chr10:101364957..101364958 29129909 RNA-Seq:(High) rs78033937 Functional Loss SNV COSMIC 33..33 33 central_nervous_system oligodendroglioma_Grade_III,frontal_lobe oligodendroglioma_Grade_III 3 brain Human_RBP_ID_11486300 54432 RMVar_ID_54432 Human_SNP_ID_808814796 A-to-I Human chr10 + 69099330 69099330 69099330 CTTTCTCTTTTGTTTTTTTTTTTTTTTGAGACAGGGTCTCCTCTGTCACCCAGGATGGAGTGCAG CTTTCTCTTTTGTTTTTTTTTTTTTTTGAGACTGGGTCTCCTCTGTCACCCAGGATGGAGTGCAG A T SRGN Ensembl:ENSG00000122862 Protein coding intron GSE100210 HepG2 cell line chr10:69099329..69099330 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast HER-positive_carcinoma 2 breast RMVar_hsa_circ_122072,RMVar_hsa_circ_143977 54433 RMVar_ID_54433 Human_SNP_ID_808858594 A-to-I Human chr10 - 114461653 114461653 114461653 CACCACACCCAGCTAATTTTTGTGTTTCTGGTAGAGACTGGGTTTCACTATGTTGGCCAGGCTGG CACCACACCCAGCTAATTTTTGTGTTTCTGGTGGAGACTGGGTTTCACTATGTTGGCCAGGCTGG T C ABLIM1 Ensembl:ENSG00000099204 Protein coding intron GSE107867 ASD brains,frontal_cortex;ASD brains,temporal_cortex chr10:114461652..114461653 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_11268449 RMVar_hsa_circ_34764,RMVar_hsa_circ_107118,RMVar_hsa_circ_122800,RMVar_hsa_circ_101470,RMVar_hsa_circ_95635,RMVar_hsa_circ_146457,RMVar_hsa_circ_89929,RMVar_hsa_circ_86375,RMVar_hsa_circ_146459,RMVar_hsa_circ_146458,RMVar_hsa_circ_146455,RMVar_hsa_circ_146456,RMVar_hsa_circ_146454,RMVar_hsa_circ_20409,RMVar_hsa_circ_72075,RMVar_hsa_circ_115438,RMVar_hsa_circ_374856,RMVar_hsa_circ_146468,RMVar_hsa_circ_146466,RMVar_hsa_circ_146467,RMVar_hsa_circ_85284 54434 RMVar_ID_54434 Human_SNP_ID_808867614 A-to-I Human chr10 - 73452665 73452665 73452665 TTGAGACAGAGTCTTGCTCTGTCACCCAGGCTAGAGTGCAGTGGCGTGATCTCAGCTCACTGCAA TTGAGACAGAGTCTTGCTCTGTCACCCAGGCTGGAGTGCAGTGGCGTGATCTCAGCTCACTGCAA T C PPP3CB Ensembl:ENSG00000107758 Protein coding intron GSE47997 K562 cells&HepG2 cells chr10:73452664..73452665 23474544 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 4 prostate RMVar_hsa_circ_385,RMVar_hsa_circ_87356,RMVar_hsa_circ_144299,RMVar_hsa_circ_304594,RMVar_hsa_circ_144302,RMVar_hsa_circ_297628,RMVar_hsa_circ_144301,RMVar_hsa_circ_339419,RMVar_hsa_circ_286011 54435 RMVar_ID_54435 Human_SNP_ID_808887356 A-to-I Human chr10 + 68758790 68758790 68758790 TGCCTCCCGGGTTCAAGAGATTCTCGTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCCTGTG TGCCTCCCGGGTTCAAGAGATTCTCGTGCCTCGGCCTCCCGAGTAGCTGGGACTACAGGCCTGTG A G CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE100210;GSE123020:GSM3490829,GSM3490830,GSM3490831 HepG2 cell line;esophageal squamous carcinoma cells,EC109 cell line chr10:68758789..68758790 29129909,32596459 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - Human_RBP_ID_24826356 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_52772,RMVar_hsa_circ_308624 54436 RMVar_ID_54436 Human_SNP_ID_808960174 A-to-I Human chr10 + 43605134 43605134 43605134 TCCACAATGCCCACCATATCATCGAATACCAGACCAAGTTTCTTACAATTATCTACTGTAATGGA TCCACAATGCCCACCATATCATCGAATACCAGGCCAAGTTTCTTACAATTATCTACTGTAATGGA A G - - Other Unknown GSE100210 HepG2 cell line chr10:43605133..43605134 29129909 RNA-Seq:(High) rs1171331738 Functional Loss SNV ICGC 33..33 33 LAML 2 - 54437 RMVar_ID_54437 Human_SNP_ID_808986124 A-to-I Human chr10 + 102528533 102528533 102528533 TCAAGGCTGTAGTGAGCTGTGATCACGGCACTACACTCTAGCTTGGGCAACAGAGTGAGACCCTG TCAAGGCTGTAGTGAGCTGTGATCACGGCACTGCACTCTAGCTTGGGCAACAGAGTGAGACCCTG A G SUFU Ensembl:ENSG00000107882 Protein coding intron GSE100210 HepG2 cell line chr10:102528532..102528533 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 4 liver RMVar_hsa_circ_145975,RMVar_hsa_circ_109981 54438 RMVar_ID_54438 Human_SNP_ID_809140582 A-to-I Human chr10 - 70163731 70163731 70163731 TTCCATCACCATCTTTGTCAAATAGTGAAAAAACTTCTTTGAATTCTACAATCTGCTCCTCAGTC TTCCATCACCATCTTTGTCAAATAGTGAAAAAGCTTCTTTGAATTCTACAATCTGCTCCTCAGTC T C SAR1A Ensembl:ENSG00000079332 Protein coding intron GSE100210 HepG2 cell line chr10:70163730..70163731 29129909 RNA-Seq:(High) rs879068471 Functional Loss SNV ICGC,COSMIC 33..33 33 ESCA,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 5 haematopoietic and lymphoid tissue RMVar_hsa_circ_105466,RMVar_hsa_circ_144047 54439 RMVar_ID_54439 Human_SNP_ID_809146508 A-to-I Human chr10 - 77847835 77847835 77847835 AGGTGTGGTGGGGCGTGTCTGTGGTCCCAGCTACTTGGGAGGCGGAGGCAGGAGGATCACTTGAG AGGTGTGGTGGGGCGTGTCTGTGGTCCCAGCTCCTTGGGAGGCGGAGGCAGGAGGATCACTTGAG T G DLG5 Ensembl:ENSG00000151208 Protein coding intron GSE100210 HepG2 cell line chr10:77847834..77847835 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 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_144531 54440 RMVar_ID_54440 Human_SNP_ID_809155673 A-to-I Human chr10 + 68758155 68758155 68758155 TGGCTCACTGCAGCTTTGGCCTCCTGGGTTCAAATGATTCTTGTGCCTCAGCCTCTCGAATAGCT TGGCTCACTGCAGCTTTGGCCTCCTGGGTTCATATGATTCTTGTGCCTCAGCCTCTCGAATAGCT A T CCAR1 Ensembl:ENSG00000060339 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line chr10:68758155..68758156 29129909,31158229,31158229 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_9603897,Human_RBP_ID_11401552 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_52772,RMVar_hsa_circ_308624 54441 RMVar_ID_54441 Human_SNP_ID_809155921 A-to-I Human chr10 + 12395724 12395724 12395724 ATTACTTGAGGTCAGGAGTTCGAGACCAGCCTAGCCAACATGGTGAAAAATACAAAAATTAGCCA ATTACTTGAGGTCAGGAGTTCGAGACCAGCCTTGCCAACATGGTGAAAAATACAAAAATTAGCCA A T CAMK1D Ensembl:ENSG00000183049 Protein coding intron GSE100210 HepG2 cell line chr10:12395723..12395724 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 3 prostate RMVar_hsa_circ_344991,RMVar_hsa_circ_357603 54442 RMVar_ID_54442 Human_SNP_ID_809225379 A-to-I Human chr10 - 119572339 119572338 119572339 GAAACCCCATCTCTACTAAAAATAACAAAAAAATTAGCTGGGCGTGCTGGTGGGCGCTGGTAGTC GAAACCCCATCTCTACTAAAAATAACAAAAAA_TTAGCTGGGCGTGCTGGTGGGCGCTGGTAGTC AT A TIAL1 Ensembl:ENSG00000151923 Protein coding 3'UTR GSE100210 HepG2 cell line chr10:119572338..119572339 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 33..33 33 LICA 1 - 54443 RMVar_ID_54443 Human_SNP_ID_809236025 A-to-I Human chr10 - 101785892 101785892 101785892 CAGTTATTCTGCTTTTTGTAAAGCCGTGGCCAATTGTCTCCTGTAATGACTGTTGGTTCAGGCAT CAGTTATTCTGCTTTTTGTAAAGCCGTGGCCAGTTGTCTCCTGTAATGACTGTTGGTTCAGGCAT T C OGA Ensembl:ENSG00000198408 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr10:101785891..101785892 30559470 RNA-Seq:(High) rs530554255 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 3 liver Human_RBP_ID_368368,Human_RBP_ID_1440336,Human_RBP_ID_1758773,Human_RBP_ID_2186125,Human_RBP_ID_3336625,Human_RBP_ID_4102958,Human_RBP_ID_5138372,Human_RBP_ID_5918454,Human_RBP_ID_8324177,Human_RBP_ID_8756889,Human_RBP_ID_11237450,Human_RBP_ID_19459045,Human_RBP_ID_21882400,Human_RBP_ID_22787234,Human_RBP_ID_23429629,Human_RBP_ID_27602013 Human_miRNA_ID_2026268,Human_miRNA_ID_2215911,Human_miRNA_ID_2675082,Human_miRNA_ID_2925833 RMVar_hsa_circ_145752,RMVar_hsa_circ_91447,RMVar_hsa_circ_95524,RMVar_hsa_circ_145753 54444 RMVar_ID_54444 Human_SNP_ID_809249447 A-to-I Human chr10 + 82977438 82977438 82977438 TGAGACCAGCCTGGCCAACATGGTGAAACCTCATCTCTACTAAAAATACAAAAATTAGCCTGCCA TGAGACCAGCCTGGCCAACATGGTGAAACCTCGTCTCTACTAAAAATACAAAAATTAGCCTGCCA A G NRG3 Ensembl:ENSG00000185737 Protein coding intron GSE47997 K562 cells&HepG2 cells chr10:82977437..82977438 23474544 RNA-Seq:(High) rs368694060 Functional Loss SNV ICGC 33..33 33 COCA 1 - RMVar_hsa_circ_5793,RMVar_hsa_circ_267768,RMVar_hsa_circ_345711,RMVar_hsa_circ_144643,RMVar_hsa_circ_144642,RMVar_hsa_circ_52312,RMVar_hsa_circ_144646,RMVar_hsa_circ_144647 54445 RMVar_ID_54445 Human_SNP_ID_809288838 A-to-I Human chr10 - 93313164 93313164 93313164 GACTTGCGTCACACGATCATTCCTGCAAAATCACCAGAGAAATGCAGATTGGACATGATTCCGGA GACTTGCGTCACACGATCATTCCTGCAAAATCGCCAGAGAAATGCAGATTGGACATGATTCCGGA T C MYOF Ensembl:ENSG00000138119 Protein coding 3'UTR GSE100210 HepG2 cell line chr10:93313163..93313164 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 pancreas ductal_carcinoma 2 pancreas Human_RBP_ID_27154 Human_Splice_Rec_1160662,Human_Splice_Rec_1160768,Human_Splice_Rec_1160872 Human_miRNA_ID_953793 RMVar_hsa_circ_88542,RMVar_hsa_circ_106860,RMVar_hsa_circ_89315,RMVar_hsa_circ_285603,RMVar_hsa_circ_145082,RMVar_hsa_circ_357618,RMVar_hsa_circ_125510,RMVar_hsa_circ_145084,RMVar_hsa_circ_145085,RMVar_hsa_circ_105349,RMVar_hsa_circ_305537,RMVar_hsa_circ_145086,RMVar_hsa_circ_145087,RMVar_hsa_circ_145088 54446 RMVar_ID_54446 Human_SNP_ID_809338396 A-to-I Human chr10 - 102428621 102428621 102428621 CCTCAGCCTCCCAAAGTGCTGGAATTACAGGCATGAGGCACCGTGCCCAGCCAAGGAAGGGAATT CCTCAGCCTCCCAAAGTGCTGGAATTACAGGCTTGAGGCACCGTGCCCAGCCAAGGAAGGGAATT T A CUEDC2 Ensembl:ENSG00000107874 Protein coding intron GSE100210 HepG2 cell line chr10:102428620..102428621 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 54447 RMVar_ID_54447 Human_SNP_ID_809348323 A-to-I Human chr10 + 60792032 60792032 60792032 GAAACCACTTTTCCATGGGGATTCAGAAATTGATCAACTCTTCAGGATTTTCAGGTAGCTATTAA GAAACCACTTTTCCATGGGGATTCAGAAATTGGTCAACTCTTCAGGATTTTCAGGTAGCTATTAA A G CDK1 Ensembl:ENSG00000170312 Protein coding CDS GSE100210 HepG2 cell line chr10:60792031..60792032 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,colon adenocarcinoma,large_intestine adenocarcinoma 7 large intestine Human_RBP_ID_274227,Human_RBP_ID_983604,Human_RBP_ID_1447978,Human_RBP_ID_1768176,Human_RBP_ID_3353371,Human_RBP_ID_5983409,Human_RBP_ID_8336315,Human_RBP_ID_8761819,Human_RBP_ID_17227506,Human_RBP_ID_17779631,Human_RBP_ID_18187922,Human_RBP_ID_18595674,Human_RBP_ID_22029280,Human_RBP_ID_22432416,Human_RBP_ID_22752389,Human_RBP_ID_27609065 Human_Splice_Rec_1137115,Human_Splice_Rec_1137131,Human_Splice_Rec_1137145,Human_Splice_Rec_1137157,Human_Splice_Rec_1137167 RMVar_hsa_circ_13223,RMVar_hsa_circ_339113,RMVar_hsa_circ_30189 54448 RMVar_ID_54448 Human_SNP_ID_809365981 A-to-I Human chr10 - 114461227 114461227 114461227 CCCCATCTCTACCAAAAATACAAAAAAAAATTAGCCGGGCATGGTGGTGCGTGCCTGAAGTCCCA CCCCATCTCTACCAAAAATACAAAAAAAAATTCGCCGGGCATGGTGGTGCGTGCCTGAAGTCCCA T G ABLIM1 Ensembl:ENSG00000099204 Protein coding intron GSE107867 ASD brains,cerebellum chr10:114461226..114461227 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_34764,RMVar_hsa_circ_107118,RMVar_hsa_circ_122800,RMVar_hsa_circ_101470,RMVar_hsa_circ_95635,RMVar_hsa_circ_146457,RMVar_hsa_circ_89929,RMVar_hsa_circ_86375,RMVar_hsa_circ_146459,RMVar_hsa_circ_146458,RMVar_hsa_circ_146455,RMVar_hsa_circ_146456,RMVar_hsa_circ_146454,RMVar_hsa_circ_20409,RMVar_hsa_circ_72075,RMVar_hsa_circ_115438,RMVar_hsa_circ_374856,RMVar_hsa_circ_146468,RMVar_hsa_circ_146466,RMVar_hsa_circ_146467,RMVar_hsa_circ_85284 54449 RMVar_ID_54449 Human_SNP_ID_809374987 A-to-I Human chr10 - 17223101 17223101 17223101 TGTCCTTTGTAGCAACACGGATACAAGTAGAAACCATAAACCTAAGCAAATTAATGCAGAAACAG TGTCCTTTGTAGCAACACGGATACAAGTAGAACCCATAAACCTAAGCAAATTAATGCAGAAACAG T G VIM-AS1 Ensembl:ENSG00000229124 lincRNA intron GSE100210 HepG2 cell line chr10:17223100..17223101 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 54450 RMVar_ID_54450 Human_SNP_ID_809378448 A-to-I Human chr10 + 74325881 74325881 74325881 GTGCTGGCTTTTTTTTTTCTTTTTTAAGACAGAGTCTCTCTCTGTCACCCAGGCTGAGGTGCAGA GTGCTGGCTTTTTTTTTTCTTTTTTAAGACAGGGTCTCTCTCTGTCACCCAGGCTGAGGTGCAGA A G ADK Ensembl:ENSG00000156110 Protein coding intron GSE100210 HepG2 cell line chr10:74325880..74325881 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_11429309 RMVar_hsa_circ_348285,RMVar_hsa_circ_124476,RMVar_hsa_circ_144422,RMVar_hsa_circ_55084,RMVar_hsa_circ_60984,RMVar_hsa_circ_282801,RMVar_hsa_circ_352531,RMVar_hsa_circ_79561,RMVar_hsa_circ_144426,RMVar_hsa_circ_46815,RMVar_hsa_circ_144425 54451 RMVar_ID_54451 Human_SNP_ID_809400495 A-to-I Human chr10 - 124762463 124762463 124762463 TTTCCACTTCAGCCTCCCGAGTAGGTGGAACTACAGGCACACATCATCATGCCTGGATAATTTTT TTTCCACTTCAGCCTCCCGAGTAGGTGGAACTGCAGGCACACATCATCATGCCTGGATAATTTTT T C AC068896.3,EEF1AKMT2 Ensembl:ENSG00000258539,Ensembl:ENSG00000203791 Protein coding,Protein coding intron,intron GSE38233;GSE56152;GSE100210 cultured B-cells;embryonic stem cells,wild type;HepG2 cell line chr10:124762462..124762463 24183664,25708366,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 colon adenocarcinoma,LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia,large_intestine adenocarcinoma 3 large intestine,haematopoietic and lymphoid tissue Human_Splice_Rec_1186510,Human_Splice_Rec_1186522,Human_Splice_Rec_1186538 RMVar_hsa_circ_333711,RMVar_hsa_circ_96352,RMVar_hsa_circ_113129,RMVar_hsa_circ_66558,RMVar_hsa_circ_94477,RMVar_hsa_circ_146966,RMVar_hsa_circ_146967,RMVar_hsa_circ_146968,RMVar_hsa_circ_146971,RMVar_hsa_circ_146970,RMVar_hsa_circ_278620,RMVar_hsa_circ_360501,RMVar_hsa_circ_146969,RMVar_hsa_circ_355304,RMVar_hsa_circ_277321,RMVar_hsa_circ_89000 54452 RMVar_ID_54452 Human_SNP_ID_809411906 A-to-I Human chr10 + 68544528 68544528 68544528 GATGTCATCAACATACGAACTCCAACTTTGGCAGCCATCAGCAAACTGGCACCTGCAATTAAACC GATGTCATCAACATACGAACTCCAACTTTGGCGGCCATCAGCAAACTGGCACCTGCAATTAAACC A G - - Other Unknown GSE100210 HepG2 cell line chr10:68544527..68544528 29129909 RNA-Seq:(High) rs878858980 Functional Loss SNV ICGC 33..33 33 COCA 1 - 54453 RMVar_ID_54453 Human_SNP_ID_809425376 A-to-I Human chr10 + 74355095 74355095 74355095 TGTCTCCTCCTGTCTTGGTCTCCCAATGTGCTAGAACTACGGGCATGAGACACTGCACCTGCTCT TGTCTCCTCCTGTCTTGGTCTCCCAATGTGCTCGAACTACGGGCATGAGACACTGCACCTGCTCT A C ADK Ensembl:ENSG00000156110 Protein coding intron GSE100210 HepG2 cell line chr10:74355094..74355095 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_348285,RMVar_hsa_circ_124476,RMVar_hsa_circ_144422,RMVar_hsa_circ_55084,RMVar_hsa_circ_60984,RMVar_hsa_circ_282801,RMVar_hsa_circ_352531,RMVar_hsa_circ_79561,RMVar_hsa_circ_144426,RMVar_hsa_circ_46815,RMVar_hsa_circ_144425 54454 RMVar_ID_54454 Human_SNP_ID_809478670 A-to-I Human chr10 + 74105308 74105308 74105308 CCTCTGATGAATTGAGCAAAACCATCTCCCCGATGGTGATGGATGCAAAAGCTGTGGCTGGAAAC CCTCTGATGAATTGAGCAAAACCATCTCCCCGGTGGTGATGGATGCAAAAGCTGTGGCTGGAAAC A G VCL Ensembl:ENSG00000035403 Protein coding exon GSE100210 HepG2 cell line chr10:74105307..74105308 29129909 RNA-Seq:(High) rs774388320 Functional Loss SNV COSMIC 33..33 33 haematopoietic_and_lymphoid_tissue chronic_myeloid_leukaemia 2 haematopoietic and lymphoid tissue Human_RBP_ID_22432081,Human_RBP_ID_22752458,Human_RBP_ID_23206471,Human_RBP_ID_26396807 Human_Splice_Rec_1148215,Human_Splice_Rec_1148253,Human_Splice_Rec_1148295,Human_Splice_Rec_1148343,Human_Splice_Rec_1148357 RMVar_hsa_circ_39033,RMVar_hsa_circ_35196,RMVar_hsa_circ_51471,RMVar_hsa_circ_566,RMVar_hsa_circ_15566,RMVar_hsa_circ_34602,RMVar_hsa_circ_52858,RMVar_hsa_circ_21536 54455 RMVar_ID_54455 Human_SNP_ID_809577704 A-to-I Human chr10 + 103447271 103447271 103447271 GAGTGGGAGGCCCTGGTTCTCACGGTACAAGTAGACGCCGGTGATGGCATTCCACTGTGGCCGTG GAGTGGGAGGCCCTGGTTCTCACGGTACAAGTGGACGCCGGTGATGGCATTCCACTGTGGCCGTG A G - - Other Unknown GSE38233 cultured B-cells chr10:103447270..103447271 24183664 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 mouth squamous_cell_carcinoma 4 head and neck 54456 RMVar_ID_54456 Human_SNP_ID_809585157 A-to-I Human chr10 + 68131613 68131613 68131613 ATAGCTTACTGTAATCTTGAACTCCCAGGTTCAGGTGATCCTCCTGCCTGGTTGTCCTGAGTAGC ATAGCTTACTGTAATCTTGAACTCCCAGGTTCTGGTGATCCTCCTGCCTGGTTGTCCTGAGTAGC A T MYPN Ensembl:ENSG00000138347 Protein coding intron GSE100210 HepG2 cell line chr10:68131612..68131613 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 6 large intestine RMVar_hsa_circ_107930,RMVar_hsa_circ_143722,RMVar_hsa_circ_21761 54457 RMVar_ID_54457 Human_SNP_ID_809587186 A-to-I Human chr10 - 63253495 63253495 63253495 CCTGTATTCCCAGCTACTCGGGAGTCTGAGGCAGGAGAATCGTTTGAGCCCGGGAGGCAGAGGTT CCTGTATTCCCAGCTACTCGGGAGTCTGAGGCGGGAGAATCGTTTGAGCCCGGGAGGCAGAGGTT T C JMJD1C Ensembl:ENSG00000171988 Protein coding intron GSE107867 ASD brains,cerebellum chr10:63253494..63253495 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_68824,RMVar_hsa_circ_51781,RMVar_hsa_circ_24971,RMVar_hsa_circ_14996,RMVar_hsa_circ_328149 54458 RMVar_ID_54458 Human_SNP_ID_809611426 A-to-I Human chr10 - 32925928 32925928 32925928 AATGAACTTGTTGGAAAACAGCGCATATCTGGAAATTTGGATTCTCCAGAAGGTGGTTTCGATGC AATGAACTTGTTGGAAAACAGCGCATATCTGGGAATTTGGATTCTCCAGAAGGTGGTTTCGATGC T C ITGB1 Ensembl:ENSG00000150093 Protein coding CDS GSE100210 HepG2 cell line chr10:32925927..32925928 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_1446289,Human_RBP_ID_1765900,Human_RBP_ID_4118284,Human_RBP_ID_17787329,Human_RBP_ID_22431679,Human_RBP_ID_22752797,Human_RBP_ID_23454021 Human_Splice_Rec_1124191,Human_Splice_Rec_1124219,Human_Splice_Rec_1124251 Human_miRNA_ID_2792732 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_4380,RMVar_hsa_circ_69112,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 54459 RMVar_ID_54459 Human_SNP_ID_809612400 A-to-I Human chr10 - 14937812 14937809 14937813 TTGGCTCACTGCAACCTCTACCTCCTGGTTTCAAGCGATTCTCTTGCCTCAGCCTCCTGAGTAGC TTGGCTCACTGCAACCTCTACCTCCTGGTTT__AGCGATTCTCTTGCCTCAGCCTCCTGAGTAGC GCTTG GCT DCLRE1C Ensembl:ENSG00000152457 Protein coding intron GSE38233 cultured B-cells chr10:14937811..14937812 24183664 RNA-Seq:(High) - Functional Loss DEL ICGC 32..33 33 BRCA 1 - RMVar_hsa_circ_95450,RMVar_hsa_circ_44299,RMVar_hsa_circ_18230,RMVar_hsa_circ_294230,RMVar_hsa_circ_142327,RMVar_hsa_circ_142329,RMVar_hsa_circ_333598,RMVar_hsa_circ_297947,RMVar_hsa_circ_58901,RMVar_hsa_circ_5704,RMVar_hsa_circ_352602,RMVar_hsa_circ_332014,RMVar_hsa_circ_142330 54460 RMVar_ID_54460 Human_SNP_ID_809621101 A-to-I Human chr10 - 124786694 124786694 124786694 GCGATTTTCCTGCCTCAGCCTCCTGAGTAGCTAGGATTACAGGCGTACACCATGCCTGGTTAATT GCGATTTTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCGTACACCATGCCTGGTTAATT T C AC068896.3,EEF1AKMT2 Ensembl:ENSG00000258539,Ensembl:ENSG00000203791 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells chr10:124786693..124786694 24183664 RNA-Seq:(High) rs1189182194 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue RMVar_hsa_circ_96352,RMVar_hsa_circ_113129,RMVar_hsa_circ_146967,RMVar_hsa_circ_146968,RMVar_hsa_circ_146971,RMVar_hsa_circ_355304,RMVar_hsa_circ_277321,RMVar_hsa_circ_89000,RMVar_hsa_circ_58897,RMVar_hsa_circ_146973,RMVar_hsa_circ_317308 54461 RMVar_ID_54461 Human_SNP_ID_809657502 A-to-I Human chr10 - 7582052 7582051 7582052 GCCAACATGGTGAAACCCGTCTCTACTAAAAAAGTACAAAAATTAGCCAGGCATGGTGGCGTGTG GCCAACATGGTGAAACCCGTCTCTACTAAAAA_GTACAAAAATTAGCCAGGCATGGTGGCGTGTG CT C ITIH5 Ensembl:ENSG00000123243 Protein coding intron GSE47997 K562 cells&HepG2 cells chr10:7582051..7582052 23474544 RNA-Seq:(High) - Functional Loss DEL ICGC 33..33 33 ESCA 1 - 54462 RMVar_ID_54462 Human_SNP_ID_809693598 A-to-I Human chr10 - 11458873 11458873 11458873 ATGGGGTTTCACTCTCTCACCCAGACTGGAGTACAGTGGGGAGATCTCAGCTCACTGCAGCCTCT ATGGGGTTTCACTCTCTCACCCAGACTGGAGTGCAGTGGGGAGATCTCAGCTCACTGCAGCCTCT T C USP6NL Ensembl:ENSG00000148429 Protein coding 3'UTR GSE100210 HepG2 cell line chr10:11458872..11458873 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 2 pancreas 54463 RMVar_ID_54463 Human_SNP_ID_809747098 A-to-I Human chr10 + 73776534 73776534 73776534 GCAAGACCTTGTCTCTAAAAAATAAAAGAATTAGCAGGGCATGGTGGTGCACACCTGTAGCCCTA GCAAGACCTTGTCTCTAAAAAATAAAAGAATTGGCAGGGCATGGTGGTGCACACCTGTAGCCCTA A G FUT11 Ensembl:ENSG00000196968 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr10:73776533..73776534 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_11426113,Human_RBP_ID_26398437 54464 RMVar_ID_54464 Human_SNP_ID_809806017 A-to-I Human chr10 + 5752512 5752512 5752512 TGCCCACTGGGTCTGTCTCAGACTTCACTTACATCACTTCTGCTGATTTCCTGCGCTAACTCCAG TGCCCACTGGGTCTGTCTCAGACTTCACTTACGTCACTTCTGCTGATTTCCTGCGCTAACTCCAG A G TASOR2 Ensembl:ENSG00000108021 Protein coding intron GSE38233 cultured B-cells chr10:5752511..5752512 24183664 RNA-Seq:(High) rs2669138 Functional Loss SNV COSMIC 33..33 33 central_nervous_system oligodendroglioma_Grade_III,frontal_lobe oligodendroglioma_Grade_III 2 brain GWAS_ID_4335,GWAS_ID_4336,GWAS_ID_4337,GWAS_ID_4338,GWAS_ID_4339,GWAS_ID_4340,GWAS_ID_4341 RMVar_hsa_circ_105337,RMVar_hsa_circ_92584,RMVar_hsa_circ_34796,RMVar_hsa_circ_141752,RMVar_hsa_circ_141751,RMVar_hsa_circ_7481,RMVar_hsa_circ_50210,RMVar_hsa_circ_111415,RMVar_hsa_circ_141764,RMVar_hsa_circ_69481,RMVar_hsa_circ_62192,RMVar_hsa_circ_69725,RMVar_hsa_circ_121611,RMVar_hsa_circ_141769 54465 RMVar_ID_54465 Human_SNP_ID_809807948 A-to-I Human chr10 - 63222247 63222247 63222247 ATCTCGACAGCTCTCCCTGTTACATCCTGTAAATCATCTTGATGCTTTTGAACCCCCCTATAAAT ATCTCGACAGCTCTCCCTGTTACATCCTGTAAGTCATCTTGATGCTTTTGAACCCCCCTATAAAT T C JMJD1C Ensembl:ENSG00000171988 Protein coding intron GSE100210 HepG2 cell line chr10:63222246..63222247 29129909 RNA-Seq:(High) rs1185970367 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 haematopoietic and lymphoid tissue RMVar_hsa_circ_68824,RMVar_hsa_circ_51781,RMVar_hsa_circ_24971,RMVar_hsa_circ_14996,RMVar_hsa_circ_328149 54466 RMVar_ID_54466 Human_SNP_ID_809838525 A-to-I Human chr10 - 29527551 29527551 29527551 GTGGTGGTGCGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATCACTTGACCCCG GTGGTGGTGCGCGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCACTTGACCCCG T C SVIL Ensembl:ENSG00000197321 Protein coding intron GSE47997 K562 cells&HepG2 cells chr10:29527550..29527551 23474544 RNA-Seq:(High) rs922323346 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue RMVar_hsa_circ_22771,RMVar_hsa_circ_142885,RMVar_hsa_circ_126998,RMVar_hsa_circ_64840,RMVar_hsa_circ_361448,RMVar_hsa_circ_15950,RMVar_hsa_circ_18215,RMVar_hsa_circ_334511,RMVar_hsa_circ_331556,RMVar_hsa_circ_32975,RMVar_hsa_circ_142887,RMVar_hsa_circ_72217,RMVar_hsa_circ_142886,RMVar_hsa_circ_18678,RMVar_hsa_circ_362967,RMVar_hsa_circ_123646 54467 RMVar_ID_54467 Human_SNP_ID_809889024 A-to-I Human chr10 - 73249207 73249207 73249207 AAGGAAAAATAATATAAAGATACCATTGGGGCAGTGGCTCACACCTGTAATCTCAGCACTTTGGG AAGGAAAAATAATATAAAGATACCATTGGGGCGGTGGCTCACACCTGTAATCTCAGCACTTTGGG T C MRPS16 Ensembl:ENSG00000182180 Protein coding exon GSE38233;GSE100210;GSE107867;GSE123020:GSM3490829,GSM3490830,GSM3490831;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;ASD brains,cerebellum;esophageal squamous carcinoma cells,EC109 cell line;esophageal squamous carcinoma cells,KYSE180 cell line chr10:73249206..73249207 24183664,29129909,30559470,32596459,32596459 RNA-Seq:(High) rs563025614 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 haematopoietic and lymphoid tissue Human_RBP_ID_8172668,Human_RBP_ID_26398410 RMVar_hsa_circ_82619,RMVar_hsa_circ_127977,RMVar_hsa_circ_144275,RMVar_hsa_circ_144276 54468 RMVar_ID_54468 Human_SNP_ID_809891695 A-to-I Human chr10 - 73248973 73248973 73248973 CCGATGCTGCAGTGAACTGTGATTGTTCCACTACAGTCCAGCCTGGGTGACAGAGAAAAGAAAAA CCGATGCTGCAGTGAACTGTGATTGTTCCACTGCAGTCCAGCCTGGGTGACAGAGAAAAGAAAAA T C MRPS16 Ensembl:ENSG00000182180 Protein coding exon GSE38233;GSE100210;GSE112787 cultured B-cells;HepG2 cell line;293 Flip-In T-REx cells,empty vector chr10:73248972..73248973 24183664,29129909,29967493 RNA-Seq:(High) rs1133556 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 haematopoietic and lymphoid tissue Human_RBP_ID_382131,Human_RBP_ID_1449806,Human_RBP_ID_3356805,Human_RBP_ID_4127005,Human_RBP_ID_5998321,Human_RBP_ID_8338775,Human_RBP_ID_22155502,Human_RBP_ID_23468496,Human_RBP_ID_24831877,Human_RBP_ID_26398405 Human_miRNA_ID_291237,Human_miRNA_ID_1980706,Human_miRNA_ID_1982430,Human_miRNA_ID_2541881,Human_miRNA_ID_2543755,Human_miRNA_ID_2545605,Human_miRNA_ID_2547460,Human_miRNA_ID_2549324,Human_miRNA_ID_2551193,Human_miRNA_ID_2556600,Human_miRNA_ID_2558482,Human_miRNA_ID_2588901 RMVar_hsa_circ_82619,RMVar_hsa_circ_127977,RMVar_hsa_circ_144275,RMVar_hsa_circ_144276 54469 RMVar_ID_54469 Human_SNP_ID_809927883 A-to-I Human chr10 + 6181038 6181037 6181039 ATTTTATTTTCATTTGTAATTATTTTAGAGACAGAGTCTGGCTCTGTCGCTCAGGCTGGAGTGCA ATTTTATTTTCATTTGTAATTATTTTAGAGAC__AGTCTGGCTCTGTCGCTCAGGCTGGAGTGCA CAG C PFKFB3 Ensembl:ENSG00000170525 Protein coding intron GSE100210 HepG2 cell line chr10:6181037..6181038 29129909 RNA-Seq:(High) rs933368841 Functional Loss DEL ICGC 33..34 33 ESCA 1 - Human_RBP_ID_11383452 RMVar_hsa_circ_141817,RMVar_hsa_circ_98825 54470 RMVar_ID_54470 Human_SNP_ID_872170542 A-to-I Human chr8 + 94792699 94792699 94792699 TAACACGGTGAAACCCCGTCTCTACTGAAAATACAAAAAATTAGCCGGGCAGGGTGGCGGGCGCC TAACACGGTGAAACCCCGTCTCTACTGAAAATGCAAAAAATTAGCCGGGCAGGGTGGCGGGCGCC A G DPY19L4 Ensembl:ENSG00000156162 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line chr8:94792698..94792699 24183664,29129909,31158229,32596459 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 54471 RMVar_ID_54471 Human_SNP_ID_872179084 A-to-I Human chr8 - 47592206 47592206 47592206 CAAATGATGTAGCAGAGCAGTGGAAGACCAACAAAGCCCAAGCCATAGAAACAGCTAGAGCATGA CAAATGATGTAGCAGAGCAGTGGAAGACCAACGAAGCCCAAGCCATAGAAACAGCTAGAGCATGA T C AC024451.3 Ensembl:ENSG00000254065 Pseudogene exon GSE100210 HepG2 cell line chr8:47592205..47592206 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 8 haematopoietic and lymphoid tissue Human_miRNA_ID_1826336,Human_miRNA_ID_1826539 54472 RMVar_ID_54472 Human_SNP_ID_872217636 A-to-I Human chr8 - 65715395 65715394 65715395 CCAGCCTAGGTGACAGAGCAAGACTCTGTCTCAAAAAAAAAAAAAAAACTTTTTTATAGAGACAG CCAGCCTAGGTGACAGAGCAAGACTCTGTCTC_AAAAAAAAAAAAAAACTTTTTTATAGAGACAG TT T PDE7A Ensembl:ENSG00000205268 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells chr8:65715394..65715395 23474544 RNA-Seq:(High) - Functional Loss DEL ICGC 33..33 33 LMS 1 - 54473 RMVar_ID_54473 Human_SNP_ID_872364608 A-to-I Human chr8 + 39122287 39122287 39122287 ATGAATTGAATTGTGTCCCCCGCCAAATCCATATGTTGAAAACCAAACTCCCAGTATGGAGATAG ATGAATTGAATTGTGTCCCCCGCCAAATCCATTTGTTGAAAACCAAACTCCCAGTATGGAGATAG A T ADAM32 Ensembl:ENSG00000197140 Protein coding intron GSE100210 HepG2 cell line chr8:39122286..39122287 29129909 RNA-Seq:(High) rs1413174967 Functional Loss SNV ICGC 33..33 33 RECA 1 - RMVar_hsa_circ_251491,RMVar_hsa_circ_297124,RMVar_hsa_circ_355861,RMVar_hsa_circ_363722,RMVar_hsa_circ_298602,RMVar_hsa_circ_330952,RMVar_hsa_circ_297208,RMVar_hsa_circ_44609,RMVar_hsa_circ_284154,RMVar_hsa_circ_251493,RMVar_hsa_circ_251494,RMVar_hsa_circ_251492 54474 RMVar_ID_54474 Human_SNP_ID_872429797 A-to-I Human chr8 - 133507140 133507140 133507140 TGTCACCTGGCATCTGATTCAAACACCAAATTACTTGGACTCCAGAGTCTAGAACACGTTTCTTA TGTCACCTGGCATCTGATTCAAACACCAAATTGCTTGGACTCCAGAGTCTAGAACACGTTTCTTA T C ST3GAL1 Ensembl:ENSG00000008513 Protein coding intron GSE100210 HepG2 cell line chr8:133507139..133507140 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_94238,RMVar_hsa_circ_254566,RMVar_hsa_circ_48025 54475 RMVar_ID_54475 Human_SNP_ID_872460818 A-to-I Human chr8 + 13006802 13006802 13006802 CTGATTCTCCTGCCTCAGACTCCCAAATAGCTATGATTACAGGCACCCGCCACCACGCCCAGCTA CTGATTCTCCTGCCTCAGACTCCCAAATAGCTGTGATTACAGGCACCCGCCACCACGCCCAGCTA A G TRMT9B Ensembl:ENSG00000250305 Protein coding intron GSE107867 ASD brains,cerebellum chr8:13006801..13006802 30559470 RNA-Seq:(High) rs959735538 Functional Loss SNV ICGC 33..33 33 PAAD 1 - 54476 RMVar_ID_54476 Human_SNP_ID_872562409 A-to-I Human chr8 - 130062891 130062891 130062891 ATAGTTCACTGTAGCCTTGGACCCTGGGCTCAAGCAATCCTCCAGTCTCAGTCTCCCGAGTAGCT ATAGTTCACTGTAGCCTTGGACCCTGGGCTCATGCAATCCTCCAGTCTCAGTCTCCCGAGTAGCT T A ASAP1 Ensembl:ENSG00000153317 Protein coding intron GSE100210 HepG2 cell line chr8:130062890..130062891 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LUAD 1 - RMVar_hsa_circ_8573,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_254371 54477 RMVar_ID_54477 Human_SNP_ID_872580689 A-to-I Human chr8 + 41542134 41542134 41542134 AGCCAGGCATGGTGACTCAAGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGCGGATCATG AGCCAGGCATGGTGACTCAAGCCTGTAATCCCGGCACTTTGGGAGGCCGAGGCGGGCGGATCATG A G GINS4 Ensembl:ENSG00000147536 Protein coding 3'UTR GSE47997;GSE38233;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;cultured B-cells;Bronchiolar epithelium,BERP35T4 cell line chr8:41542133..41542134 23474544,24183664,31158229 RNA-Seq:(High) rs1411825517 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue Human_miRNA_ID_2086094,Human_miRNA_ID_2845718,Human_miRNA_ID_2848738 RMVar_hsa_circ_86479,RMVar_hsa_circ_251525 54478 RMVar_ID_54478 Human_SNP_ID_872674581 A-to-I Human chr8 + 66456096 66456094 66456097 AGGAAGTCGAGGCTGCATTGAGCTATGATCACACCATTGCACTTTAGCCTGGGTGACAGAGTGAG AGGAAGTCGAGGCTGCATTGAGCTATGATCA___CATTGCACTTTAGCCTGGGTGACAGAGTGAG ACAC A AC009879.3,ADHFE1 Ensembl:ENSG00000285791,Ensembl:ENSG00000147576 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line chr8:66456095..66456096 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 32..34 33 PAAD 1 - RMVar_hsa_circ_73979,RMVar_hsa_circ_74777 54479 RMVar_ID_54479 Human_SNP_ID_872686924 A-to-I Human chr8 + 103477462 103477462 103477462 CCAAGTAATCCTCCTCAGCCTCTGGAGAAGCTAGGACCACAGACACACACCACCACGCCCAGGTA CCAAGTAATCCTCCTCAGCCTCTGGAGAAGCTGGGACCACAGACACACACCACCACGCCCAGGTA A G - - Other Unknown GSE100210 HepG2 cell line chr8:103477461..103477462 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 54480 RMVar_ID_54480 Human_SNP_ID_872781533 A-to-I Human chr8 - 74604194 74604194 74604194 GAAGGTGGATTAAATATCACTCTCACCATCCGACTACTTATGCATGGAAAGGAAGTTGGCAGTAT GAAGGTGGATTAAATATCACTCTCACCATCCGGCTACTTATGCATGGAAAGGAAGTTGGCAGTAT T C AC115837.1 Ensembl:ENSG00000253341 Pseudogene exon GSE100210 HepG2 cell line chr8:74604193..74604194 29129909 RNA-Seq:(High) rs879008325 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_3170018,Human_RBP_ID_7870845 Human_miRNA_ID_1895024 54481 RMVar_ID_54481 Human_SNP_ID_872791500 A-to-I Human chr8 + 51911498 51911498 51911498 CCCACTGCAACCTTGAACACCTGGGCTCAAGCAATCCTCCTGCCTCAGCCTCCTGAGTAGCTGGG CCCACTGCAACCTTGAACACCTGGGCTCAAGCGATCCTCCTGCCTCAGCCTCCTGAGTAGCTGGG A G AC064807.1 Ensembl:ENSG00000228801 lincRNA intron GSE100210 HepG2 cell line chr8:51911497..51911498 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_Splice_Rec_976874 54482 RMVar_ID_54482 Human_SNP_ID_872822407 A-to-I Human chr8 - 102854010 102854010 102854010 TTGAACCCGGGAGGCGGAGGTTGCAGTGAGCCAAGATGGTGCCACCGCACTGTAGACTAGGAGAC TTGAACCCGGGAGGCGGAGGTTGCAGTGAGCCTAGATGGTGCCACCGCACTGTAGACTAGGAGAC T A AZIN1 Ensembl:ENSG00000155096 Protein coding intron GSE100210 HepG2 cell line chr8:102854009..102854010 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_253717,RMVar_hsa_circ_374327,RMVar_hsa_circ_71944,RMVar_hsa_circ_57983,RMVar_hsa_circ_253719,RMVar_hsa_circ_56739,RMVar_hsa_circ_299900,RMVar_hsa_circ_124698,RMVar_hsa_circ_253735,RMVar_hsa_circ_288571,RMVar_hsa_circ_253742,RMVar_hsa_circ_318159 54483 RMVar_ID_54483 Human_SNP_ID_872852681 A-to-I Human chr8 + 125335850 125335850 125335850 ACTAGGCATTGCTCAACCAAAGGGGAAAGTTCAAAGTGAATAGGTAGGTTGGTGTGTCATCTAAA ACTAGGCATTGCTCAACCAAAGGGGAAAGTTCGAAGTGAATAGGTAGGTTGGTGTGTCATCTAAA A G NSMCE2 Ensembl:ENSG00000156831 Protein coding intron GSE47997 K562 cells&HepG2 cells chr8:125335849..125335850 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 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 54484 RMVar_ID_54484 Human_SNP_ID_872864600 A-to-I Human chr8 - 22630541 22630538 22630542 TCAAAATCTGCCGTGAAGATATCCTTGGACTTACTCTCCAATCCCCTCTGTGAGCAAGACCAGGA TCAAAATCTGCCGTGAAGATATCCTTGGACT____CTCCAATCCCCTCTGTGAGCAAGACCAGGA GAGTA G BIN3 Ensembl:ENSG00000147439 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector chr8:22630540..22630541 29967493 RNA-Seq:(High) - Functional Loss DEL ICGC 32..35 33 THCA 1 - Human_RBP_ID_5514667,Human_RBP_ID_9405263,Human_RBP_ID_16393239,Human_RBP_ID_18115736,Human_RBP_ID_19021842 Human_Splice_Rec_957800,Human_Splice_Rec_957801,Human_Splice_Rec_957816,Human_Splice_Rec_957817,Human_Splice_Rec_957828,Human_Splice_Rec_957829,Human_Splice_Rec_957842,Human_Splice_Rec_957843,Human_Splice_Rec_957856,Human_Splice_Rec_957857,Human_Splice_Rec_957876,Human_Splice_Rec_957877,Human_Splice_Rec_957888,Human_Splice_Rec_957889,Human_Splice_Rec_957898,Human_Splice_Rec_957899,Human_Splice_Rec_957908,Human_Splice_Rec_957909 RMVar_hsa_circ_113595,RMVar_hsa_circ_250762 54485 RMVar_ID_54485 Human_SNP_ID_872864625 A-to-I Human chr8 - 16752532 16752532 16752532 AAAATAGCTGGGCATGGTGGCATGTGCCCATAATCCCAGCTCTTTGGGAGTCTGAGGCAGGAGAA AAAATAGCTGGGCATGGTGGCATGTGCCCATACTCCCAGCTCTTTGGGAGTCTGAGGCAGGAGAA T G AC011586.2 Ensembl:ENSG00000253496 lincRNA intron GSE100210 HepG2 cell line chr8:16752531..16752532 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 54486 RMVar_ID_54486 Human_SNP_ID_872867859 A-to-I Human chr8 - 51854953 51854953 51854953 TCAGGCTCGTCTCGAACTCCCGACTTCGGGTGATCCACCCTCCTTGGCCTCCCAAAGTGCTTGGA TCAGGCTCGTCTCGAACTCCCGACTTCGGGTGGTCCACCCTCCTTGGCCTCCCAAAGTGCTTGGA T C PCMTD1 Ensembl:ENSG00000168300 Protein coding intron GSE100210 HepG2 cell line chr8:51854952..51854953 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - Human_RBP_ID_16433951 RMVar_hsa_circ_252047,RMVar_hsa_circ_295213,RMVar_hsa_circ_124656,RMVar_hsa_circ_252045,RMVar_hsa_circ_252046,RMVar_hsa_circ_252052,RMVar_hsa_circ_252051,RMVar_hsa_circ_370827,RMVar_hsa_circ_295411,RMVar_hsa_circ_252050 54487 RMVar_ID_54487 Human_SNP_ID_872917849 A-to-I Human chr8 - 74604235 74604235 74604235 AGCTCCCCAGAACACTGCTCGACATGGAAACCAGTGTGATTGAAGGTGGATTAAATATCACTCTC AGCTCCCCAGAACACTGCTCGACATGGAAACCGGTGTGATTGAAGGTGGATTAAATATCACTCTC T C AC115837.1 Ensembl:ENSG00000253341 Pseudogene exon GSE107867 ASD brains,temporal_cortex chr8:74604234..74604235 30559470 RNA-Seq:(High) rs879065967 Functional Loss SNV ICGC 33..33 33 LAML 2 - 54488 RMVar_ID_54488 Human_SNP_ID_872918557 A-to-I Human chr8 + 86504266 86504266 86504266 AGAAGAGGAGAATGCTAAGTAGATCCTCCAGCAGTTGTGGGGCACCCAGGATGTATCCCAAGACA AGAAGAGGAGAATGCTAAGTAGATCCTCCAGCGGTTGTGGGGCACCCAGGATGTATCCCAAGACA A G SLC2A3P4 Ensembl:ENSG00000254088 Pseudogene exon GSE100210 HepG2 cell line chr8:86504265..86504266 29129909 RNA-Seq:(High) rs990686357 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 10 haematopoietic and lymphoid tissue 54489 RMVar_ID_54489 Human_SNP_ID_873014094 A-to-I Human chr8 + 94742505 94742505 94742505 ACCTCTGGCTCATGGATGCAAGTGATTCTCCCACCTCAGCCTCCCCAGTAGCTGGGACCACAGGC ACCTCTGGCTCATGGATGCAAGTGATTCTCCCCCCTCAGCCTCCCCAGTAGCTGGGACCACAGGC A C DPY19L4 Ensembl:ENSG00000156162 Protein coding intron GSE100210 HepG2 cell line chr8:94742504..94742505 29129909 RNA-Seq:(High) rs1044867126 Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 2 pancreas RMVar_hsa_circ_61206,RMVar_hsa_circ_91878,RMVar_hsa_circ_101288,RMVar_hsa_circ_70419,RMVar_hsa_circ_253147,RMVar_hsa_circ_50616,RMVar_hsa_circ_253148,RMVar_hsa_circ_306558,RMVar_hsa_circ_340330,RMVar_hsa_circ_370143,RMVar_hsa_circ_72374,RMVar_hsa_circ_20647,RMVar_hsa_circ_30857,RMVar_hsa_circ_253150,RMVar_hsa_circ_341217 54490 RMVar_ID_54490 Human_SNP_ID_873064437 A-to-I Human chr8 - 8235297 8235297 8235297 CGACTACAGGCATGCGCCACCATGTCCGGCTAATTTTTGTACTTTTTTTTGAGACAGAGTTTCGT CGACTACAGGCATGCGCCACCATGTCCGGCTACTTTTTGTACTTTTTTTTGAGACAGAGTTTCGT T G - - Other Unknown GSE100210 HepG2 cell line chr8:8235296..8235297 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_16479096 54491 RMVar_ID_54491 Human_SNP_ID_873217135 A-to-I Human chr8 + 30332100 30332100 30332100 CGAAAGTCCACAGATTATCACAGAATCTGTACATATTTAGAAAGCTCCTGAAATTGACTCTGTTC CGAAAGTCCACAGATTATCACAGAATCTGTACTTATTTAGAAAGCTCCTGAAATTGACTCTGTTC A T - - Other Unknown GSE100210 HepG2 cell line chr8:30332099..30332100 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LMS 1 - 54492 RMVar_ID_54492 Human_SNP_ID_873387045 A-to-I Human chr8 + 19824301 19824301 19824301 ATCACTTGAGGTCAGGAGTTCGAGACCAGCCTAGCCAACATGGTGAAACCCCATCTCTACTAAAA ATCACTTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAA A G INTS10 Ensembl:ENSG00000104613 Protein coding intron GSE47997 K562 cells&HepG2 cells chr8:19824300..19824301 23474544 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 1 prostate RMVar_hsa_circ_44149,RMVar_hsa_circ_250550,RMVar_hsa_circ_279393,RMVar_hsa_circ_43432,RMVar_hsa_circ_64903,RMVar_hsa_circ_364148,RMVar_hsa_circ_316230,RMVar_hsa_circ_317210,RMVar_hsa_circ_331901,RMVar_hsa_circ_56654,RMVar_hsa_circ_54056,RMVar_hsa_circ_250551,RMVar_hsa_circ_53253,RMVar_hsa_circ_323157,RMVar_hsa_circ_250549,RMVar_hsa_circ_316960,RMVar_hsa_circ_46349,RMVar_hsa_circ_250558,RMVar_hsa_circ_295440,RMVar_hsa_circ_352527,RMVar_hsa_circ_250553,RMVar_hsa_circ_250554,RMVar_hsa_circ_250555,RMVar_hsa_circ_354569,RMVar_hsa_circ_357807,RMVar_hsa_circ_320990,RMVar_hsa_circ_326765,RMVar_hsa_circ_300220,RMVar_hsa_circ_250560,RMVar_hsa_circ_250559,RMVar_hsa_circ_250564,RMVar_hsa_circ_250557,RMVar_hsa_circ_282663,RMVar_hsa_circ_283331,RMVar_hsa_circ_343049,RMVar_hsa_circ_85764,RMVar_hsa_circ_250562,RMVar_hsa_circ_250563,RMVar_hsa_circ_250561 54493 RMVar_ID_54493 Human_SNP_ID_873461549 A-to-I Human chr8 - 124674380 124674380 124674380 GACAGCTCCTGGCGATGCGTGGGGTGTACCATATATAGTGACGCTGATGCAGATTATGCATATTT GACAGCTCCTGGCGATGCGTGGGGTGTACCATGTATAGTGACGCTGATGCAGATTATGCATATTT T C MTSS1 Ensembl:ENSG00000170873 Protein coding intron GSE47997 K562 cells&HepG2 cells chr8:124674379..124674380 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_55907,RMVar_hsa_circ_254259,RMVar_hsa_circ_91018 54494 RMVar_ID_54494 Human_SNP_ID_873479659 A-to-I Human chr8 + 39021552 39021552 39021552 GTGATCTACCCGCCTGGGCCTCTCAAAATGCTAGAATTACAGGCATGAGGTACTGCACCCGGCCT GTGATCTACCCGCCTGGGCCTCTCAAAATGCTGGAATTACAGGCATGAGGTACTGCACCCGGCCT A G ADAM9 Ensembl:ENSG00000168615 Protein coding intron GSE100210 HepG2 cell line chr8:39021551..39021552 29129909 RNA-Seq:(High) rs1326388254 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue 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_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 54495 RMVar_ID_54495 Human_SNP_ID_873504439 A-to-I Human chr8 - 47592174 47592174 47592174 AAAGCCCAAGCCATAGAAACAGCTAGAGCATGAACTAGGCTATATGCCATGAATAATATTTAAAT AAAGCCCAAGCCATAGAAACAGCTAGAGCATGGACTAGGCTATATGCCATGAATAATATTTAAAT T C AC024451.3 Ensembl:ENSG00000254065 Pseudogene exon GSE100210 HepG2 cell line chr8:47592173..47592174 29129909 RNA-Seq:(High) rs1488114464 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 8 haematopoietic and lymphoid tissue Human_RBP_ID_7840343 54496 RMVar_ID_54496 Human_SNP_ID_873521692 A-to-I Human chr8 - 102839821 102839821 102839821 TATTTGTCTTTTTTTTTATAACCATAATAGACAGGGAAAAATGCATTTTTTGTGGGAGATCTTGG TATTTGTCTTTTTTTTTATAACCATAATAGACGGGGAAAAATGCATTTTTTGTGGGAGATCTTGG T C AZIN1 Ensembl:ENSG00000155096 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr8:102839820..102839821 30559470 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 oesophagus adenocarcinoma 2 oesophagus Human_RBP_ID_26189016 Human_Splice_Rec_998986,Human_Splice_Rec_999008,Human_Splice_Rec_999042,Human_Splice_Rec_999052 Human_miRNA_ID_343879,Human_miRNA_ID_1696180 RMVar_hsa_circ_253717,RMVar_hsa_circ_253716,RMVar_hsa_circ_374327,RMVar_hsa_circ_253722,RMVar_hsa_circ_71944,RMVar_hsa_circ_57983,RMVar_hsa_circ_253720,RMVar_hsa_circ_253719,RMVar_hsa_circ_346711,RMVar_hsa_circ_335862,RMVar_hsa_circ_253721,RMVar_hsa_circ_333854,RMVar_hsa_circ_291201,RMVar_hsa_circ_253723,RMVar_hsa_circ_253736,RMVar_hsa_circ_56739,RMVar_hsa_circ_253731,RMVar_hsa_circ_292255,RMVar_hsa_circ_301296,RMVar_hsa_circ_253732,RMVar_hsa_circ_326256,RMVar_hsa_circ_333034,RMVar_hsa_circ_275862,RMVar_hsa_circ_253734,RMVar_hsa_circ_299900,RMVar_hsa_circ_322747,RMVar_hsa_circ_285419,RMVar_hsa_circ_253738,RMVar_hsa_circ_124698,RMVar_hsa_circ_253737,RMVar_hsa_circ_27185,RMVar_hsa_circ_377862,RMVar_hsa_circ_253735,RMVar_hsa_circ_292537,RMVar_hsa_circ_253739 54497 RMVar_ID_54497 Human_SNP_ID_873540332 A-to-I Human chr8 + 37747531 37747531 37747531 ATCTCCTCTTCCTCTTCATCAATGGTAGACACAGTGACAGAACTGAACTTGCCCATGTCTTTGGT ATCTCCTCTTCCTCTTCATCAATGGTAGACACGGTGACAGAACTGAACTTGCCCATGTCTTTGGT A G ERLIN2 Ensembl:ENSG00000147475 Protein coding intron GSE100210 HepG2 cell line chr8:37747530..37747531 29129909 RNA-Seq:(High) rs879010644 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 haematopoietic and lymphoid tissue RMVar_hsa_circ_34493 54498 RMVar_ID_54498 Human_SNP_ID_873568343 A-to-I Human chr8 - 140878547 140878547 140878547 CCCTGTCACCCAGGCTGCAGTACGGTGGCATGAACATGGCTCACTGCAGCCTCTTGGGCTCAAGC CCCTGTCACCCAGGCTGCAGTACGGTGGCATGTACATGGCTCACTGCAGCCTCTTGGGCTCAAGC T A PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE47997 K562 cells&HepG2 cells chr8:140878546..140878547 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 RECA 1 - 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_254709,RMVar_hsa_circ_355189,RMVar_hsa_circ_324678,RMVar_hsa_circ_322054,RMVar_hsa_circ_254720,RMVar_hsa_circ_79843,RMVar_hsa_circ_293517,RMVar_hsa_circ_34510,RMVar_hsa_circ_2596,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_77007,RMVar_hsa_circ_286767,RMVar_hsa_circ_305313,RMVar_hsa_circ_254744,RMVar_hsa_circ_332346,RMVar_hsa_circ_288942,RMVar_hsa_circ_19264,RMVar_hsa_circ_254757,RMVar_hsa_circ_254756,RMVar_hsa_circ_349698,RMVar_hsa_circ_286717,RMVar_hsa_circ_311942,RMVar_hsa_circ_290687,RMVar_hsa_circ_279729,RMVar_hsa_circ_1973,RMVar_hsa_circ_254759,RMVar_hsa_circ_254760,RMVar_hsa_circ_254758,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_28404,RMVar_hsa_circ_5209,RMVar_hsa_circ_254773,RMVar_hsa_circ_254774,RMVar_hsa_circ_280042,RMVar_hsa_circ_282877,RMVar_hsa_circ_254781,RMVar_hsa_circ_319301,RMVar_hsa_circ_293225,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_93272,RMVar_hsa_circ_254795,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_284623,RMVar_hsa_circ_297776,RMVar_hsa_circ_364237,RMVar_hsa_circ_286215,RMVar_hsa_circ_278354,RMVar_hsa_circ_254797,RMVar_hsa_circ_254798,RMVar_hsa_circ_254796,RMVar_hsa_circ_254804,RMVar_hsa_circ_270852,RMVar_hsa_circ_254801,RMVar_hsa_circ_280309,RMVar_hsa_circ_314660,RMVar_hsa_circ_355911,RMVar_hsa_circ_254802,RMVar_hsa_circ_322669,RMVar_hsa_circ_328876,RMVar_hsa_circ_333595,RMVar_hsa_circ_274966,RMVar_hsa_circ_254806,RMVar_hsa_circ_254805,RMVar_hsa_circ_254808 54499 RMVar_ID_54499 Human_SNP_ID_873695626 A-to-I Human chr8 + 84921204 84921204 84921204 AAATGTGAAAGGCATTTATGAATGGTAAGGGAAACACTATATACAAATGTATATTTGTAAAAGCT AAATGTGAAAGGCATTTATGAATGGTAAGGGAGACACTATATACAAATGTATATTTGTAAAAGCT A G RALYL Ensembl:ENSG00000184672 Protein coding 3'UTR GSE47997 K562 cells&HepG2 cells chr8:84921204..84921205 23474544 RNA-Seq:(High) rs10094238 Functional Loss SNV ICGC 33..33 33 ESCA 1 - GWAS_ID_5695,GWAS_ID_5696,GWAS_ID_5697,GWAS_ID_5698,GWAS_ID_5699,GWAS_ID_5700,GWAS_ID_5701,GWAS_ID_5702,GWAS_ID_5703,GWAS_ID_5704,GWAS_ID_5705,GWAS_ID_5706,GWAS_ID_5707,GWAS_ID_5708,GWAS_ID_5709,GWAS_ID_5710,GWAS_ID_5711,GWAS_ID_5712,GWAS_ID_5713,GWAS_ID_5714,GWAS_ID_5715,GWAS_ID_5716,GWAS_ID_5717,GWAS_ID_5718,GWAS_ID_5719,GWAS_ID_5720,GWAS_ID_5721,GWAS_ID_5722,GWAS_ID_5723,GWAS_ID_5724,GWAS_ID_5725,GWAS_ID_5726,GWAS_ID_5727,GWAS_ID_5728,GWAS_ID_5729,GWAS_ID_5730,GWAS_ID_5731,GWAS_ID_5732,GWAS_ID_5733,GWAS_ID_5734 54500 RMVar_ID_54500 Human_SNP_ID_873882086 A-to-I Human chr8 - 133507144 133507144 133507144 CTACTGTCACCTGGCATCTGATTCAAACACCAAATTACTTGGACTCCAGAGTCTAGAACACGTTT CTACTGTCACCTGGCATCTGATTCAAACACCACATTACTTGGACTCCAGAGTCTAGAACACGTTT T G ST3GAL1 Ensembl:ENSG00000008513 Protein coding intron GSE100210 HepG2 cell line chr8:133507143..133507144 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 STAD 1 - RMVar_hsa_circ_94238,RMVar_hsa_circ_254566,RMVar_hsa_circ_48025 54501 RMVar_ID_54501 Human_SNP_ID_873884433 A-to-I Human chr8 + 86504070 86504070 86504070 TTGGCACTCTCAACCAGCTGGGCATCATTGTCAGAATTCTGGTGGCCCAGATCTTTGGTCTGGAA TTGGCACTCTCAACCAGCTGGGCATCATTGTCGGAATTCTGGTGGCCCAGATCTTTGGTCTGGAA A G SLC2A3P4 Ensembl:ENSG00000254088 Pseudogene exon GSE100210 HepG2 cell line chr8:86504069..86504070 29129909 RNA-Seq:(High) rs1258624474 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 5 haematopoietic and lymphoid tissue Human_RBP_ID_8274225 54502 RMVar_ID_54502 Human_SNP_ID_873888533 A-to-I Human chr8 + 12565650 12565621 12565650 CTGGGGAGAGAGACAGTGTAAAAGAGAGAGAGAGAGAGAGACCGTAAAAGAAGGGAGACAAAGAG CTGG_____________________________GAGAGAGACCGTAAAAGAAGGGAGACAAAGAG GGGAGAGAGACAGTGTAAAAGAGAGAGAGA G 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 GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr8:12565649..12565650 30559470 RNA-Seq:(High) - Functional Loss DEL ICGC 5..33 33 SKCA 1 - RMVar_hsa_circ_250269,RMVar_hsa_circ_105727 54503 RMVar_ID_54503 Human_SNP_ID_873983449 A-to-I Human chr8 + 94868788 94868788 94868788 CGCCTGCAAGGTTCAAGCGATTCTCATGCCTCAGCCTGCCAAGTATCTGGGATTACAGGTGCATG CGCCTGCAAGGTTCAAGCGATTCTCATGCCTCGGCCTGCCAAGTATCTGGGATTACAGGTGCATG A G INTS8 Ensembl:ENSG00000164941 Protein coding intron GSE100210 HepG2 cell line chr8:94868787..94868788 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_Splice_Rec_994514,Human_Splice_Rec_994515,Human_Splice_Rec_994568,Human_Splice_Rec_994569,Human_Splice_Rec_994660,Human_Splice_Rec_994661 RMVar_hsa_circ_18428,RMVar_hsa_circ_348538,RMVar_hsa_circ_253162,RMVar_hsa_circ_33694,RMVar_hsa_circ_253174,RMVar_hsa_circ_340579,RMVar_hsa_circ_43348,RMVar_hsa_circ_337784,RMVar_hsa_circ_298527,RMVar_hsa_circ_67572,RMVar_hsa_circ_253199,RMVar_hsa_circ_39008,RMVar_hsa_circ_360896,RMVar_hsa_circ_71669,RMVar_hsa_circ_71463,RMVar_hsa_circ_57612,RMVar_hsa_circ_99978,RMVar_hsa_circ_343453,RMVar_hsa_circ_366057,RMVar_hsa_circ_253207,RMVar_hsa_circ_253208,RMVar_hsa_circ_269310,RMVar_hsa_circ_278144,RMVar_hsa_circ_253210,RMVar_hsa_circ_57723,RMVar_hsa_circ_281304,RMVar_hsa_circ_253211 54504 RMVar_ID_54504 Human_SNP_ID_874051586 A-to-I Human chr8 - 94492798 94492798 94492798 TTATGACTGCAGGTAAAGGTTGACTTAATTGAACTCTCTGAAAAATGCTGTAGTGACTTTGATTT TTATGACTGCAGGTAAAGGTTGACTTAATTGACCTCTCTGAAAAATGCTGTAGTGACTTTGATTT T G VIRMA Ensembl:ENSG00000164944 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector chr8:94492797..94492798 29967493 RNA-Seq:(High) rs772231079 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 OV,ovary serous_carcinoma 3 ovary Human_RBP_ID_705972,Human_RBP_ID_8692240,Human_RBP_ID_8922478,Human_RBP_ID_24272328 Human_Splice_Rec_993890,Human_Splice_Rec_993908,Human_Splice_Rec_993938,Human_Splice_Rec_993952 Human_miRNA_ID_652078 RMVar_hsa_circ_102204,RMVar_hsa_circ_125301,RMVar_hsa_circ_69380,RMVar_hsa_circ_289600,RMVar_hsa_circ_253108,RMVar_hsa_circ_322018,RMVar_hsa_circ_51210,RMVar_hsa_circ_81033,RMVar_hsa_circ_253111,RMVar_hsa_circ_37180,RMVar_hsa_circ_253110 54505 RMVar_ID_54505 Human_SNP_ID_874098289 A-to-I Human chr8 + 69129969 69129969 69129969 ACATTGCGGAAAAGGCTGACCGCAAATACGAGAAGGTAGCTCGTAAGCTGGTCATCCTGGAGGGT ACATTGCGGAAAAGGCTGACCGCAAATACGAGGAGGTAGCTCGTAAGCTGGTCATCCTGGAGGGT A G AF201337.1 Ensembl:ENSG00000254332 Pseudogene exon GSE100210 HepG2 cell line chr8:69129968..69129969 29129909 RNA-Seq:(High) rs575790564 Functional Loss SNV ICGC 33..33 33 LUSC 2 - Human_RBP_ID_17715133,Human_RBP_ID_18125508 54506 RMVar_ID_54506 Human_SNP_ID_874102111 A-to-I Human chr8 + 60937932 60937932 60937932 TCCTCCGGTTTCCTCTTCTTTCTGACAAAGTGAGAAATATCAGTCACACAATTTGATGAGGAAGC TCCTCCGGTTTCCTCTTCTTTCTGACAAAGTGGGAAATATCAGTCACACAATTTGATGAGGAAGC A G AC022182.1 Ensembl:ENSG00000254777 lincRNA intron GSE100210 HepG2 cell line chr8:60937931..60937932 29129909 RNA-Seq:(High) rs878859594 Functional Loss SNV ICGC 33..33 33 LAML 2 - 54507 RMVar_ID_54507 Human_SNP_ID_874156607 A-to-I Human chr8 + 19841727 19841727 19841727 CATGCAACCATTCTGGAAACCAACTTCCCATGACCAAGTTGAACATGTCATTACCTAATTATTAA CATGCAACCATTCTGGAAACCAACTTCCCATGGCCAAGTTGAACATGTCATTACCTAATTATTAA A G INTS10 Ensembl:ENSG00000104613 Protein coding intron GSE100210 HepG2 cell line chr8:19841726..19841727 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue RMVar_hsa_circ_95876,RMVar_hsa_circ_44149,RMVar_hsa_circ_43432,RMVar_hsa_circ_364148,RMVar_hsa_circ_316230,RMVar_hsa_circ_53253,RMVar_hsa_circ_46349,RMVar_hsa_circ_250555,RMVar_hsa_circ_320990,RMVar_hsa_circ_333353,RMVar_hsa_circ_21549,RMVar_hsa_circ_7742,RMVar_hsa_circ_33642,RMVar_hsa_circ_250567,RMVar_hsa_circ_250568,RMVar_hsa_circ_299428,RMVar_hsa_circ_250571,RMVar_hsa_circ_250574,RMVar_hsa_circ_90857,RMVar_hsa_circ_250576,RMVar_hsa_circ_34646 54508 RMVar_ID_54508 Human_SNP_ID_874165605 A-to-I Human chr8 + 39021484 39021484 39021484 TTTTGTATTTTTAGTAGAGAGAAGGTTTCGCCATGTTGGCTAGGCTGGTCTCGAACTCCTGACCT TTTTGTATTTTTAGTAGAGAGAAGGTTTCGCCGTGTTGGCTAGGCTGGTCTCGAACTCCTGACCT A G ADAM9 Ensembl:ENSG00000168615 Protein coding intron GSE100210 HepG2 cell line chr8:39021483..39021484 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue 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_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 54509 RMVar_ID_54509 Human_SNP_ID_874179955 A-to-I Human chr8 - 119827037 119827037 119827037 AGGCACGTACCACCAGCCTGGCTAATTTTTGTATTTTTTGTAGAGACGGAGTTTTGCCATGTTGC AGGCACGTACCACCAGCCTGGCTAATTTTTGTGTTTTTTGTAGAGACGGAGTTTTGCCATGTTGC T C TAF2 Ensembl:ENSG00000064313 Protein coding intron GSE100210 HepG2 cell line chr8:119827036..119827037 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_92193,RMVar_hsa_circ_254056,RMVar_hsa_circ_254075,RMVar_hsa_circ_254077,RMVar_hsa_circ_254081,RMVar_hsa_circ_254085 54510 RMVar_ID_54510 Human_SNP_ID_874218819 A-to-I Human chr8 - 40958362 40958362 40958362 AAACTTAAGACCTAAACTGTAAAACTACTAGAAGAAAACATAGGAGAAAGCTTCATGACATTGGT AAACTTAAGACCTAAACTGTAAAACTACTAGATGAAAACATAGGAGAAAGCTTCATGACATTGGT T A - - Other Unknown GSE100210 HepG2 cell line chr8:40958361..40958362 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 54511 RMVar_ID_54511 Human_SNP_ID_874218828 A-to-I Human chr8 - 40958362 40958362 40958362 AAACTTAAGACCTAAACTGTAAAACTACTAGAAGAAAACATAGGAGAAAGCTTCATGACATTGGT AAACTTAAGACCTAAACTGTAAAACTACTAGACGAAAACATAGGAGAAAGCTTCATGACATTGGT T G - - Other Unknown GSE100210 HepG2 cell line chr8:40958361..40958362 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 54512 RMVar_ID_54512 Human_SNP_ID_874229445 A-to-I Human chr8 - 26506535 26506535 26506535 CTGCTAGGTGTCAGATAGATGGTCCCAGAGCTAGGTGCTGTGTCAGGCCCTGAAGACACAGATGA CTGCTAGGTGTCAGATAGATGGTCCCAGAGCTGGGTGCTGTGTCAGGCCCTGAAGACACAGATGA T C PNMA2 Ensembl:ENSG00000240694 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector chr8:26506534..26506535 29967493 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast lobular_carcinoma 2 breast Human_RBP_ID_1116544,Human_RBP_ID_7827305,Human_RBP_ID_8918648 54513 RMVar_ID_54513 Human_SNP_ID_874266372 A-to-I Human chr8 - 140670381 140670381 140670381 ACAATCTCAGCTCACTGCAACCTCTGCCTCCGAGGTTCAAATGACTCTCCTGCCTCAGCCTCCCG ACAATCTCAGCTCACTGCAACCTCTGCCTCCGGGGTTCAAATGACTCTCCTGCCTCAGCCTCCCG T C PTK2 Ensembl:ENSG00000169398 Protein coding intron GSE107867 ASD brains,frontal_cortex chr8:140670380..140670381 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 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_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,RMVar_hsa_circ_254703,RMVar_hsa_circ_120136 54514 RMVar_ID_54514 Human_SNP_ID_874339739 A-to-I Human chr8 + 17563006 17563006 17563006 CTACAAAACAAACAAACAAATTAGCTGCGTGTAGTGGCTCATTCCTGTAGTCCTAGCTAGTCAGG CTACAAAACAAACAAACAAATTAGCTGCGTGTGGTGGCTCATTCCTGTAGTCCTAGCTAGTCAGG A G SLC7A2 Ensembl:ENSG00000003989 Protein coding intron GSE47997 K562 cells&HepG2 cells chr8:17563005..17563006 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_123243,RMVar_hsa_circ_250403,RMVar_hsa_circ_7422 54515 RMVar_ID_54515 Human_SNP_ID_874740578 A-to-I Human chr8 + 97706822 97706822 97706822 AAGAGACAGGCTGGGCACAGTGGCTCACGCCTATGATTCCAGCACTTTGGGAGGTACTGTGGGAG AAGAGACAGGCTGGGCACAGTGGCTCACGCCTGTGATTCCAGCACTTTGGGAGGTACTGTGGGAG A G MTDH Ensembl:ENSG00000147649 Protein coding intron GSE38233 cultured B-cells chr8:97706821..97706822 24183664 RNA-Seq:(High) rs1214394833 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue RMVar_hsa_circ_69358,RMVar_hsa_circ_341218,RMVar_hsa_circ_366544,RMVar_hsa_circ_367157,RMVar_hsa_circ_253299,RMVar_hsa_circ_64711,RMVar_hsa_circ_320821,RMVar_hsa_circ_45496,RMVar_hsa_circ_61908,RMVar_hsa_circ_305474,RMVar_hsa_circ_93704,RMVar_hsa_circ_253301,RMVar_hsa_circ_253300,RMVar_hsa_circ_253306,RMVar_hsa_circ_253308,RMVar_hsa_circ_294717,RMVar_hsa_circ_314005,RMVar_hsa_circ_319909,RMVar_hsa_circ_113280,RMVar_hsa_circ_253307,RMVar_hsa_circ_253310,RMVar_hsa_circ_291386,RMVar_hsa_circ_352894,RMVar_hsa_circ_315212,RMVar_hsa_circ_267391,RMVar_hsa_circ_253309 54516 RMVar_ID_54516 Human_SNP_ID_874755072 A-to-I Human chr8 - 74604211 74604211 74604211 TGGAAACCAGTGTGATTGAAGGTGGATTAAATATCACTCTCACCATCCGACTACTTATGCATGGA TGGAAACCAGTGTGATTGAAGGTGGATTAAATGTCACTCTCACCATCCGACTACTTATGCATGGA T C AC115837.1 Ensembl:ENSG00000253341 Pseudogene exon GSE100210 HepG2 cell line chr8:74604210..74604211 29129909 RNA-Seq:(High) rs879178757 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_5629268 Human_miRNA_ID_1819044,Human_miRNA_ID_1853479 54517 RMVar_ID_54517 Human_SNP_ID_874821587 A-to-I Human chr8 - 61523583 61523583 61523583 GCTCGGTGTGGTGGCTCATGACTGTAATCCCAACACTTTGGGAGGCCGAGGCAGGCAGATCATTT GCTCGGTGTGGTGGCTCATGACTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGCAGATCATTT T C ASPH Ensembl:ENSG00000198363 Protein coding intron GSE47997 K562 cells&HepG2 cells chr8:61523582..61523583 23474544 RNA-Seq:(High) rs137949011 Functional Loss SNV ICGC 33..33 33 ESCA 1 - GWAS_ID_3882,GWAS_ID_3883,GWAS_ID_3884,GWAS_ID_3885,GWAS_ID_3886,GWAS_ID_3887,GWAS_ID_3888,GWAS_ID_3889,GWAS_ID_3890,GWAS_ID_3891,GWAS_ID_3892,GWAS_ID_3893,GWAS_ID_3894,GWAS_ID_3895,GWAS_ID_3896,GWAS_ID_3897,GWAS_ID_3898,GWAS_ID_3899,GWAS_ID_3900,GWAS_ID_3901,GWAS_ID_3902,GWAS_ID_3903,GWAS_ID_3904,GWAS_ID_3905,GWAS_ID_3906,GWAS_ID_3907,GWAS_ID_3908,GWAS_ID_3909,GWAS_ID_3910,GWAS_ID_3911,GWAS_ID_3912,GWAS_ID_3913,GWAS_ID_3914,GWAS_ID_3915,GWAS_ID_3916,GWAS_ID_3917,GWAS_ID_3918,GWAS_ID_3919,GWAS_ID_3920,GWAS_ID_3921,GWAS_ID_3922,GWAS_ID_3923 RMVar_hsa_circ_67952,RMVar_hsa_circ_94519,RMVar_hsa_circ_252300,RMVar_hsa_circ_288638,RMVar_hsa_circ_353926,RMVar_hsa_circ_356125,RMVar_hsa_circ_319389,RMVar_hsa_circ_126733,RMVar_hsa_circ_62714,RMVar_hsa_circ_252301,RMVar_hsa_circ_20680,RMVar_hsa_circ_252302,RMVar_hsa_circ_99077,RMVar_hsa_circ_252303 54518 RMVar_ID_54518 Human_SNP_ID_874993951 A-to-I Human chr8 - 102829408 102829408 102829408 CATCCTGTGATGAGCTTGATCAAATTGTGGAAAGCTGTCTTCTTCCTGAGCTGAATGTGGGAGAT CATCCTGTGATGAGCTTGATCAAATTGTGGAAGGCTGTCTTCTTCCTGAGCTGAATGTGGGAGAT T C AZIN1 Ensembl:ENSG00000155096 Protein coding CDS GSE38233;GSE56152;GSE100210;GSE107867 cultured B-cells;embryonic stem cells,wild type;HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr8:102829407..102829408 24183664,25708366,29129909,30559470 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 colon adenocarcinoma,LAML,haematopoietic_and_lymphoid_tissue diffuse_large_B_cell_lymphoma,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia,large_intestine adenocarcinoma 10 large intestine,haematopoietic and lymphoid tissue Human_RBP_ID_88681,Human_RBP_ID_692439,Human_RBP_ID_2050990,Human_RBP_ID_3129038,Human_RBP_ID_7794447,Human_RBP_ID_8676748,Human_RBP_ID_8915821,Human_RBP_ID_9218683,Human_RBP_ID_18124713,Human_RBP_ID_22464985,Human_RBP_ID_22836057 RMVar_hsa_circ_12006,RMVar_hsa_circ_253717,RMVar_hsa_circ_253716,RMVar_hsa_circ_374327,RMVar_hsa_circ_346854,RMVar_hsa_circ_253719 54519 RMVar_ID_54519 Human_SNP_ID_875081688 A-to-I Human chr8 + 86504064 86504064 86504064 GTACCTTTGGCACTCTCAACCAGCTGGGCATCATTGTCAGAATTCTGGTGGCCCAGATCTTTGGT GTACCTTTGGCACTCTCAACCAGCTGGGCATCGTTGTCAGAATTCTGGTGGCCCAGATCTTTGGT A G SLC2A3P4 Ensembl:ENSG00000254088 Pseudogene exon GSE100210 HepG2 cell line chr8:86504063..86504064 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 5 haematopoietic and lymphoid tissue Human_RBP_ID_8274225 54520 RMVar_ID_54520 Human_SNP_ID_875122857 A-to-I Human chr8 + 38241923 38241923 38241923 TAAAAATACAAAAATTAGCTGGGCATGGTGGTATGTGCCTGTAATCCCAGATCCTCAAGAGGCTG TAAAAATACAAAAATTAGCTGGGCATGGTGGTGTGTGCCTGTAATCCCAGATCCTCAAGAGGCTG A G DDHD2 Ensembl:ENSG00000085788 Protein coding intron GSE38233 cultured B-cells chr8:38241922..38241923 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_2044,RMVar_hsa_circ_343422,RMVar_hsa_circ_64088,RMVar_hsa_circ_49043,RMVar_hsa_circ_342677,RMVar_hsa_circ_49606,RMVar_hsa_circ_49346,RMVar_hsa_circ_54907,RMVar_hsa_circ_25968,RMVar_hsa_circ_362689,RMVar_hsa_circ_373005,RMVar_hsa_circ_32097,RMVar_hsa_circ_335477,RMVar_hsa_circ_32066,RMVar_hsa_circ_251371,RMVar_hsa_circ_251372 54521 RMVar_ID_54521 Human_SNP_ID_875270311 A-to-I Human chr8 - 52696879 52696879 52696879 CCCACCTCAGCCCCGCAAGTAGCTGGGAGTACAGGTGTGCACCATCATGCCTGGCTAATTTTTGT CCCACCTCAGCCCCGCAAGTAGCTGGGAGTACTGGTGTGCACCATCATGCCTGGCTAATTTTTGT T A RB1CC1 Ensembl:ENSG00000023287 Protein coding intron GSE100210 HepG2 cell line chr8:52696878..52696879 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 54522 RMVar_ID_54522 Human_SNP_ID_875661671 A-to-I Human chr8 + 128016192 128016192 128016192 CTCAGCTACTTAAGAGACTGAATAGGAGGATCACCAGAATCTGGGAGGTGGAGATTGCGGTGAAC CTCAGCTACTTAAGAGACTGAATAGGAGGATCTCCAGAATCTGGGAGGTGGAGATTGCGGTGAAC A T PVT1 Ensembl:ENSG00000249859 lincRNA intron GSE100210 HepG2 cell line chr8:128016191..128016192 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_5106803 RMVar_hsa_circ_75888,RMVar_hsa_circ_118838,RMVar_hsa_circ_254320,RMVar_hsa_circ_125092,RMVar_hsa_circ_107291,RMVar_hsa_circ_254322,RMVar_hsa_circ_115647,RMVar_hsa_circ_371319,RMVar_hsa_circ_373231,RMVar_hsa_circ_254323,RMVar_hsa_circ_254332,RMVar_hsa_circ_254333,RMVar_hsa_circ_254331,RMVar_hsa_circ_76237,RMVar_hsa_circ_254334,RMVar_hsa_circ_254335,RMVar_hsa_circ_77631,RMVar_hsa_circ_338304,RMVar_hsa_circ_254338,RMVar_hsa_circ_254339,RMVar_hsa_circ_301347,RMVar_hsa_circ_309118,RMVar_hsa_circ_80977,RMVar_hsa_circ_254341 54523 RMVar_ID_54523 Human_SNP_ID_875825927 A-to-I Human chr8 + 42325517 42325516 42325517 CCTGGCCAATATGGTGAAACACCGTCTCTACTAAAAATACAAAAATTAGCTGGGTGTAGTGGCAC CCTGGCCAATATGGTGAAACACCGTCTCTACT_AAAATACAAAAATTAGCTGGGTGTAGTGGCAC TA T IKBKB Ensembl:ENSG00000104365 Protein coding intron GSE47997 K562 cells&HepG2 cells chr8:42325516..42325517 23474544 RNA-Seq:(High) - Functional Loss DEL ICGC 33..33 33 MALY 1 - RMVar_hsa_circ_81888,RMVar_hsa_circ_251574,RMVar_hsa_circ_84512,RMVar_hsa_circ_251576,RMVar_hsa_circ_90497,RMVar_hsa_circ_29551,RMVar_hsa_circ_251577,RMVar_hsa_circ_61429,RMVar_hsa_circ_100970,RMVar_hsa_circ_251578,RMVar_hsa_circ_76976,RMVar_hsa_circ_251580 54524 RMVar_ID_54524 Human_SNP_ID_875841217 A-to-I Human chr8 + 127862528 127862528 127862528 GCTCAGTTCATAGTTCATAGCTTAGACCTCCCAAGCTCAAGAGATTCTTCCACCTCAGCCTCCCA GCTCAGTTCATAGTTCATAGCTTAGACCTCCCGAGCTCAAGAGATTCTTCCACCTCAGCCTCCCA A G PVT1 Ensembl:ENSG00000249859 lincRNA intron GSE100210 HepG2 cell line chr8:127862528..127862529 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - 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 54525 RMVar_ID_54525 Human_SNP_ID_875906722 A-to-I Human chr8 + 19841794 19841794 19841794 GTACCTCGCGTCCTAGTTGTATACCTTAGATGAGTGTTTTTCAAGCTGTGAGTTTTCATTTACAG GTACCTCGCGTCCTAGTTGTATACCTTAGATGGGTGTTTTTCAAGCTGTGAGTTTTCATTTACAG A G INTS10 Ensembl:ENSG00000104613 Protein coding intron GSE100210 HepG2 cell line chr8:19841793..19841794 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue RMVar_hsa_circ_95876,RMVar_hsa_circ_44149,RMVar_hsa_circ_43432,RMVar_hsa_circ_364148,RMVar_hsa_circ_316230,RMVar_hsa_circ_53253,RMVar_hsa_circ_46349,RMVar_hsa_circ_250555,RMVar_hsa_circ_320990,RMVar_hsa_circ_333353,RMVar_hsa_circ_21549,RMVar_hsa_circ_7742,RMVar_hsa_circ_33642,RMVar_hsa_circ_250567,RMVar_hsa_circ_250568,RMVar_hsa_circ_299428,RMVar_hsa_circ_250571,RMVar_hsa_circ_250574,RMVar_hsa_circ_90857,RMVar_hsa_circ_250576,RMVar_hsa_circ_34646 54526 RMVar_ID_54526 Human_SNP_ID_876056617 A-to-I Human chr8 - 118300800 118300800 118300800 ATATACAATTTTATGAACATGCGCTACCTATCAGTAATCTGTAATATTTAAGAATTAACAAAAAA ATATACAATTTTATGAACATGCGCTACCTATCCGTAATCTGTAATATTTAAGAATTAACAAAAAA T G SAMD12 Ensembl:ENSG00000177570 Protein coding intron GSE100210 HepG2 cell line chr8:118300799..118300800 29129909 RNA-Seq:(High) rs1351074908 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 54527 RMVar_ID_54527 Human_SNP_ID_876146505 A-to-I Human chr8 - 12116257 12116257 12116257 GCCTCTGGGCGCTCCTTGGTGGAAGGAGAGGGACTTGGTCCTGAGCCTGCCCCGGATCCACCTAC GCCTCTGGGCGCTCCTTGGTGGAAGGAGAGGGTCTTGGTCCTGAGCCTGCCCCGGATCCACCTAC T A - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr8:12116256..12116257 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - 54528 RMVar_ID_54528 Human_SNP_ID_876151708 A-to-I Human chr8 + 128003535 128003535 128003535 GCCTGACTAGTTTTTGTATTTTTTGTAGAGACAGGATTTCATCATGTTGCCCAGGCTGGTCTTGA GCCTGACTAGTTTTTGTATTTTTTGTAGAGACTGGATTTCATCATGTTGCCCAGGCTGGTCTTGA A T PVT1 Ensembl:ENSG00000249859 lincRNA intron GSE100210 HepG2 cell line chr8:128003534..128003535 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_5251703 RMVar_hsa_circ_75888,RMVar_hsa_circ_118838,RMVar_hsa_circ_254320,RMVar_hsa_circ_125092,RMVar_hsa_circ_107291,RMVar_hsa_circ_254322,RMVar_hsa_circ_115647,RMVar_hsa_circ_371319,RMVar_hsa_circ_373231,RMVar_hsa_circ_254323,RMVar_hsa_circ_254332,RMVar_hsa_circ_254333,RMVar_hsa_circ_254331,RMVar_hsa_circ_76237,RMVar_hsa_circ_254334,RMVar_hsa_circ_254335,RMVar_hsa_circ_77631,RMVar_hsa_circ_338304,RMVar_hsa_circ_19203,RMVar_hsa_circ_254337,RMVar_hsa_circ_254338,RMVar_hsa_circ_254339 54529 RMVar_ID_54529 Human_SNP_ID_876154504 A-to-I Human chr8 + 127813876 127813876 127813876 ACGATCTCGGCTCACTGCACCCTCTGCCTTCCAGGTTCAAGCAATTCTTCTGCCTCAGCCTTCTG ACGATCTCGGCTCACTGCACCCTCTGCCTTCCGGGTTCAAGCAATTCTTCTGCCTCAGCCTTCTG A G PVT1 Ensembl:ENSG00000249859 lincRNA intron GSE100210 HepG2 cell line chr8:127813875..127813876 29129909 RNA-Seq:(High) rs1370592843 Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_5105668,Human_RBP_ID_5251562,Human_RBP_ID_16353572 RMVar_hsa_circ_118838,RMVar_hsa_circ_101526,RMVar_hsa_circ_118329,RMVar_hsa_circ_254318,RMVar_hsa_circ_254319,RMVar_hsa_circ_254320 54530 RMVar_ID_54530 Human_SNP_ID_876275913 A-to-I Human chr8 - 22662877 22662877 22662877 CCGTCTTGGCCTCCCAAAGTGCTGGGATTACAAGCATGAGCCACCGCGGCCAGCCTTGTTTGTTT CCGTCTTGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCGGCCAGCCTTGTTTGTTT T C BIN3 Ensembl:ENSG00000147439 Protein coding intron GSE100210 HepG2 cell line chr8:22662876..22662877 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 4 large intestine 54531 RMVar_ID_54531 Human_SNP_ID_876278568 A-to-I Human chr8 - 55771505 55771505 55771505 TCAAGCAATCCTCCTACCTCAGCCCCCCGAGTAGCTGGGGCTACAGGCATGCCACCATGCCTGCC TCAAGCAATCCTCCTACCTCAGCCCCCCGAGTGGCTGGGGCTACAGGCATGCCACCATGCCTGCC T C TMEM68 Ensembl:ENSG00000167904 Protein coding intron GSE100210 HepG2 cell line chr8:55771504..55771505 29129909 RNA-Seq:(High) rs528531364 Functional Loss SNV ICGC 33..33 33 PBCA 1 - 54532 RMVar_ID_54532 Human_SNP_ID_876283141 A-to-I Human chr8 + 60937968 60937968 60937968 ATATCAGTCACACAATTTGATGAGGAAGCACCATCTGTTGGCTTTCTACTGGCAATCAGGAGACT ATATCAGTCACACAATTTGATGAGGAAGCACCGTCTGTTGGCTTTCTACTGGCAATCAGGAGACT A G AC022182.1 Ensembl:ENSG00000254777 lincRNA intron GSE100210 HepG2 cell line chr8:60937967..60937968 29129909 RNA-Seq:(High) rs879228102 Functional Loss SNV ICGC 33..33 33 LAML 2 - 54533 RMVar_ID_54533 Human_SNP_ID_876435459 A-to-I Human chr8 + 144843058 144843058 144843058 AGAAGATATTTAGGTGGCGTTCACACCTAATTATACACCAGAGAATTCACACCGGGGAGAAGCCT AGAAGATATTTAGGTGGCGTTCACACCTAATTGTACACCAGAGAATTCACACCGGGGAGAAGCCT A G ZNF7 Ensembl:ENSG00000147789 Protein coding CDS GSE100210 HepG2 cell line chr8:144843057..144843058 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 6 lung Human_RBP_ID_18114333,Human_RBP_ID_27123233 RMVar_hsa_circ_91295,RMVar_hsa_circ_82605,RMVar_hsa_circ_255192,RMVar_hsa_circ_255195 54534 RMVar_ID_54534 Human_SNP_ID_876627144 A-to-I Human chr8 + 84254962 84254962 84254962 AGCTCTTATGACAACACGAACAGCATGGGGGAAACTGCTTCCATGATCCAATTATCTCCACCTCG AGCTCTTATGACAACACGAACAGCATGGGGGATACTGCTTCCATGATCCAATTATCTCCACCTCG A T RALYL Ensembl:ENSG00000184672 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr8:84254962..84254963 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ER-PR-HER-positive_carcinoma,breast HER-positive_carcinoma 11 breast RMVar_hsa_circ_28132 54535 RMVar_ID_54535 Human_SNP_ID_876654536 A-to-I Human chr8 - 70118914 70118914 70118914 GGAGGCTGAGGCGGATGGATCACCTGAGGTCAAGAGTTTGAGACTAGCCTGGCTAACATGGTGAA GGAGGCTGAGGCGGATGGATCACCTGAGGTCAGGAGTTTGAGACTAGCCTGGCTAACATGGTGAA T C NCOA2 Ensembl:ENSG00000140396 Protein coding intron GSE100210 HepG2 cell line chr8:70118913..70118914 29129909 RNA-Seq:(High) rs969781163 Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 2 oesophagus RMVar_hsa_circ_111457,RMVar_hsa_circ_252638 54536 RMVar_ID_54536 Human_SNP_ID_876663592 A-to-I Human chr8 + 91917544 91917544 91917544 CCACCTCACTACTCTCCTCTGCAAGGCCTACCATGGGGGCCACTTAACCATCTGCCTTGCCCTGG CCACCTCACTACTCTCCTCTGCAAGGCCTACCGTGGGGGCCACTTAACCATCTGCCTTGCCCTGG A G MRPS16P1 Ensembl:ENSG00000229182 Pseudogene exon GSE100210 HepG2 cell line chr8:91917543..91917544 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 1 - 54537 RMVar_ID_54537 Human_SNP_ID_876729852 A-to-I Human chr8 - 63015371 63015371 63015371 TTGATTTATCAGTTCAGTCCAATTTATACTGGAAATATTTCTTCATTTCAGCAATGTTACATATT TTGATTTATCAGTTCAGTCCAATTTATACTGGGAATATTTCTTCATTTCAGCAATGTTACATATT T C GGH Ensembl:ENSG00000137563 Protein coding exon GSE100210 HepG2 cell line chr8:63015370..63015371 29129909 RNA-Seq:(High) rs201429647 Functional Loss SNV TCGA 33..33 33 CHOL 1 - Human_RBP_ID_702453,Human_RBP_ID_2056557,Human_RBP_ID_9227203,Human_RBP_ID_17318486,Human_RBP_ID_17433099,Human_RBP_ID_17546273 Human_Splice_Rec_981356,Human_Splice_Rec_981372,Human_Splice_Rec_981374 RMVar_hsa_circ_88655,RMVar_hsa_circ_252350 54538 RMVar_ID_54538 Human_SNP_ID_876766661 A-to-I Human chr8 - 56050649 56050649 56050649 CAGGTACGGGAAAAACACTCTTGGCACGAGCCATTGCTAGCCAGCTGGACTGCAATTTCTTAAAG CAGGTACGGGAAAAACACTCTTGGCACGAGCCGTTGCTAGCCAGCTGGACTGCAATTTCTTAAAG T C AC046176.1 Ensembl:ENSG00000236814 Pseudogene exon GSE100210 HepG2 cell line chr8:56050648..56050649 29129909 RNA-Seq:(High) rs879185840 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_22012957,Human_RBP_ID_22410643 Human_miRNA_ID_1876936,Human_miRNA_ID_1879943 54539 RMVar_ID_54539 Human_SNP_ID_876788527 A-to-I Human chr8 - 102384535 102384512 102384536 CACCATGCCCAGCTAATTTTTAAATTTTTTGTAGAGACGGGGTCTCATTATGTTGCCCACATTAG CACCATGCCCAGCTAATTTTTAAATTTTTTG________________________CCCACATTAG GCAACATAATGAGACCCCGTCTCTA G UBR5 Ensembl:ENSG00000104517 Protein coding intron GSE100210 HepG2 cell line chr8:102384534..102384535 29129909 RNA-Seq:(High) rs561761215 Functional Loss DEL ICGC 32..55 33 ESCA 1 - Human_RBP_ID_16506154 RMVar_hsa_circ_100046,RMVar_hsa_circ_253635,RMVar_hsa_circ_115812,RMVar_hsa_circ_253697,RMVar_hsa_circ_77218,RMVar_hsa_circ_253708 54540 RMVar_ID_54540 Human_SNP_ID_876860133 A-to-I Human chr8 + 97708686 97708686 97708686 CAGTGGCATGATCTCGGCTCTCTGCAACCTCCACCTCCCAGGTTCAAGTGATTCTCCCTCCTCAG CAGTGGCATGATCTCGGCTCTCTGCAACCTCCCCCTCCCAGGTTCAAGTGATTCTCCCTCCTCAG A C MTDH Ensembl:ENSG00000147649 Protein coding intron GSE38233 cultured B-cells chr8:97708685..97708686 24183664 RNA-Seq:(High) rs1387523695 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue RMVar_hsa_circ_69358,RMVar_hsa_circ_341218,RMVar_hsa_circ_366544,RMVar_hsa_circ_367157,RMVar_hsa_circ_253299,RMVar_hsa_circ_64711,RMVar_hsa_circ_320821,RMVar_hsa_circ_45496,RMVar_hsa_circ_61908,RMVar_hsa_circ_305474,RMVar_hsa_circ_93704,RMVar_hsa_circ_253301,RMVar_hsa_circ_253300,RMVar_hsa_circ_253306,RMVar_hsa_circ_253308,RMVar_hsa_circ_294717,RMVar_hsa_circ_314005,RMVar_hsa_circ_319909,RMVar_hsa_circ_113280,RMVar_hsa_circ_253307,RMVar_hsa_circ_253310,RMVar_hsa_circ_291386,RMVar_hsa_circ_352894,RMVar_hsa_circ_315212,RMVar_hsa_circ_267391,RMVar_hsa_circ_253309 54541 RMVar_ID_54541 Human_SNP_ID_876949671 A-to-I Human chr8 + 30570671 30570671 30570671 TTGAAAAACCCTTGCCCAGTTTTGATCCCTTCAAGACTTTGTCACAGCCTCTATCACACATCTGT TTGAAAAACCCTTGCCCAGTTTTGATCCCTTCGAGACTTTGTCACAGCCTCTATCACACATCTGT A G RBPMS Ensembl:ENSG00000157110 Protein coding 3'UTR GSE100210 HepG2 cell line chr8:30570671..30570672 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 5 uterus Human_RBP_ID_89888,Human_RBP_ID_26189339 Human_Splice_Rec_963356,Human_Splice_Rec_963374,Human_Splice_Rec_963390,Human_Splice_Rec_963486,Human_Splice_Rec_963502,Human_Splice_Rec_963508,Human_Splice_Rec_963512,Human_Splice_Rec_963514,Human_Splice_Rec_963518 Human_miRNA_ID_1266364,Human_miRNA_ID_1691261 54542 RMVar_ID_54542 Human_SNP_ID_877048175 A-to-I Human chr8 - 56069578 56069578 56069578 AAGAGGAACTATGGCTGGGCGGGGTGGCTCACACCTGTAATCTCAGCACTTTGGGAGGCCAAGGT AAGAGGAACTATGGCTGGGCGGGGTGGCTCACGCCTGTAATCTCAGCACTTTGGGAGGCCAAGGT T C RPS20 Ensembl:ENSG00000008988 Protein coding intron GSE100210 HepG2 cell line chr8:56069577..56069578 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 2 large intestine 54543 RMVar_ID_54543 Human_SNP_ID_813969459 A-to-I Human chr12 + 79180948 79180948 79180948 GCAGTTACCTCCATGCTGTCCTCATGATAGCGAGTGAGTTCTCTCGAGAGCTGATGGTTTTATAA GCAGTTACCTCCATGCTGTCCTCATGATAGCGCGTGAGTTCTCTCGAGAGCTGATGGTTTTATAA A C SYT1 Ensembl:ENSG00000067715 Protein coding intron GSE107867 ASD brains,frontal_cortex chr12:79180947..79180948 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 5 liver RMVar_hsa_circ_36430,RMVar_hsa_circ_51947,RMVar_hsa_circ_333141,RMVar_hsa_circ_47417,RMVar_hsa_circ_343651,RMVar_hsa_circ_42570,RMVar_hsa_circ_308387,RMVar_hsa_circ_74479 54544 RMVar_ID_54544 Human_SNP_ID_813984063 A-to-I Human chr12 - 31688557 31688557 31688557 GCAATCCGCCTGCCTTGGCCTCCCAAAGTGCTAGGATTACAGACGTTAGCTGCCGCGCCCGGCCT GCAATCCGCCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGACGTTAGCTGCCGCGCCCGGCCT T C AMN1 Ensembl:ENSG00000151743 Protein coding intron GSE100210 HepG2 cell line chr12:31688556..31688557 29129909 RNA-Seq:(High) rs904916669 Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 5 prostate 54545 RMVar_ID_54545 Human_SNP_ID_814000039 A-to-I Human chr12 - 109940816 109940816 109940816 GGAGTGCAGTAGTACGATCTCATCTCACTGCAACCTCCGCCTCCTAGGCTCAAGAGATCATCTCA GGAGTGCAGTAGTACGATCTCATCTCACTGCAGCCTCCGCCTCCTAGGCTCAAGAGATCATCTCA T C GIT2 Ensembl:ENSG00000139436 Protein coding intron GSE100210 HepG2 cell line chr12:109940815..109940816 29129909 RNA-Seq:(High) rs1255216151 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 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 54546 RMVar_ID_54546 Human_SNP_ID_814003930 A-to-I Human chr12 + 56149338 56149338 56149338 GGATTCTCATGCCTCAGGCTCCCAAGTAGCTGAGATTGCAGGCGCCTGCCACCACGCCTGGCTAA GGATTCTCATGCCTCAGGCTCCCAAGTAGCTGCGATTGCAGGCGCCTGCCACCACGCCTGGCTAA A C - - Other Unknown GSE100210 HepG2 cell line chr12:56149337..56149338 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 54547 RMVar_ID_54547 Human_SNP_ID_814006989 A-to-I Human chr12 + 12762026 12762026 12762026 ATGCCTGGCTAATTTTTTGAATTTCTTTTTGTAGAGGTGGGATCTTGCTATGTTGCCCAGGCTGC ATGCCTGGCTAATTTTTTGAATTTCTTTTTGTGGAGGTGGGATCTTGCTATGTTGCCCAGGCTGC A G APOLD1 Ensembl:ENSG00000178878 Protein coding intron GSE100210 HepG2 cell line chr12:12762025..12762026 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - 54548 RMVar_ID_54548 Human_SNP_ID_814007561 A-to-I Human chr12 + 2888627 2888627 2888627 TCACCTTACTGCAACCACCACTTCCTGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCCAGTAGC TCACCTTACTGCAACCACCACTTCCTGGGTTCTAGCGATTCTCCTGCCTCAGCCTCCCCAGTAGC A T RHNO1,TULP3 Ensembl:ENSG00000171792,Ensembl:ENSG00000078246 Protein coding,Protein coding 3'UTR,intron GSE100210 HepG2 cell line chr12:2888627..2888628 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_113281,Human_RBP_ID_418022,Human_RBP_ID_8247635 RMVar_hsa_circ_127855,RMVar_hsa_circ_154349 54549 RMVar_ID_54549 Human_SNP_ID_814015286 A-to-I Human chr12 + 121987600 121987600 121987600 AGCCAGGCATGGTGGCGCACACCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCT AGCCAGGCATGGTGGCGCACACCTGTAATCCCGGCTACTCGGGAGGCTGAGGCAGGAGAATCGCT A G WDR66 Ensembl:ENSG00000158023 Protein coding intron GSE47997 K562 cells&HepG2 cells chr12:121987599..121987600 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 2 breast RMVar_hsa_circ_160980 54550 RMVar_ID_54550 Human_SNP_ID_814024358 A-to-I Human chr12 - 11150810 11150810 11150810 ACTGATATCTTTTTTCATTATTATTATACTTTAAGTTTTAGGGTACATGTGCACAATGTGCAGGT ACTGATATCTTTTTTCATTATTATTATACTTTTAGTTTTAGGGTACATGTGCACAATGTGCAGGT T A AC018630.2,PRH1,TAS2R14 Ensembl:ENSG00000275778,Ensembl:ENSG00000231887,Ensembl:ENSG00000212127 Protein coding,Protein coding,Protein coding intron,intron,intron GSE100210 HepG2 cell line chr12:11150809..11150810 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_6245692 RMVar_hsa_circ_114046,RMVar_hsa_circ_154886 54551 RMVar_ID_54551 Human_SNP_ID_814032514 A-to-I Human chr12 + 63822640 63822640 63822640 TCGGAGAAGACATGGATGATGAGCGCCTTAAGAATCTCTTTGGCAAGTTTGGGCCTGCCTTAAAT TCGGAGAAGACATGGATGATGAGCGCCTTAAGGATCTCTTTGGCAAGTTTGGGCCTGCCTTAAAT A G PABPC1P4 Ensembl:ENSG00000255642 Pseudogene exon GSE100210 HepG2 cell line chr12:63822639..63822640 29129909 RNA-Seq:(High) rs1347493559 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_425395,Human_RBP_ID_2347680,Human_RBP_ID_4258378,Human_RBP_ID_6239657,Human_RBP_ID_26423901,Human_RBP_ID_26910112 54552 RMVar_ID_54552 Human_SNP_ID_814044329 A-to-I Human chr12 + 64450291 64450291 64450291 CTCCTGCCTCAGCATCCAGACTAGCTGTGATTACAGGTGTGCACCACCACACCCAGCTACATTTT CTCCTGCCTCAGCATCCAGACTAGCTGTGATTGCAGGTGTGCACCACCACACCCAGCTACATTTT A G XPOT Ensembl:ENSG00000184575 Protein coding 3'UTR GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line chr12:64450290..64450291 24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_26418882 Human_miRNA_ID_1398895 54553 RMVar_ID_54553 Human_SNP_ID_814057403 A-to-I Human chr12 - 6967675 6967673 6967676 AGGCCGAGGGTGAGGCCGAGGCTGCCAAGATGATATCCTTCTGCTGGAGAGATCTCAGCCCAGCC AGGCCGAGGGTGAGGCCGAGGCTGCCAAGAT___ATCCTTCTGCTGGAGAGATCTCAGCCCAGCC TATC T PHB2 Ensembl:ENSG00000215021 Protein coding intron GSE38233 cultured B-cells chr12:6967674..6967675 24183664 RNA-Seq:(High) - Functional Loss DEL TCGA 32..34 33 UCEC 1 - Human_RBP_ID_427512,Human_RBP_ID_17830213,Human_RBP_ID_18633131,Human_RBP_ID_22574100,Human_RBP_ID_22908969,Human_RBP_ID_27425022 RMVar_hsa_circ_6926,RMVar_hsa_circ_121658,RMVar_hsa_circ_125056,RMVar_hsa_circ_112548,RMVar_hsa_circ_116151,RMVar_hsa_circ_154674,RMVar_hsa_circ_154678,RMVar_hsa_circ_89625,RMVar_hsa_circ_93446,RMVar_hsa_circ_154679,RMVar_hsa_circ_154676,RMVar_hsa_circ_154677,RMVar_hsa_circ_154675,RMVar_hsa_circ_154680,RMVar_hsa_circ_374995,RMVar_hsa_circ_311995,RMVar_hsa_circ_154681 54554 RMVar_ID_54554 Human_SNP_ID_814058984 A-to-I Human chr12 + 7607068 7607068 7607068 AGAACGCTTGGAAGCCCTTGATGCCAATTCTCAGAAGCAAGAAGCAGAGTGGAAAGAAAAGGCAA AGAACGCTTGGAAGCCCTTGATGCCAATTCTCGGAAGCAAGAAGCAGAGTGGAAAGAAAAGGCAA A G AC006927.1 Ensembl:ENSG00000255977 Pseudogene exon GSE100210 HepG2 cell line chr12:7607067..7607068 29129909 RNA-Seq:(High) rs879042960 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_17358195,Human_RBP_ID_18527209 Human_miRNA_ID_1896592 54555 RMVar_ID_54555 Human_SNP_ID_814059654 A-to-I Human chr12 - 64338781 64338781 64338781 GGCCTAGCTTTGCTCTCACCATGGCTCTCAGCAATGCTGACATGCAAAAGCAGATAAAGCATATG GGCCTAGCTTTGCTCTCACCATGGCTCTCAGCGATGCTGACATGCAAAAGCAGATAAAGCATATG T C AC135279.3,C12orf56 Ensembl:ENSG00000256293,Ensembl:ENSG00000185306 Pseudogene,Protein coding exon,intron GSE100210 HepG2 cell line chr12:64338780..64338781 29129909 RNA-Seq:(High) rs878863191 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 haematopoietic and lymphoid tissue Human_miRNA_ID_1853119 RMVar_hsa_circ_53606 54556 RMVar_ID_54556 Human_SNP_ID_814061182 A-to-I Human chr12 + 12790103 12790103 12790103 TCGGCTCACTGCAACCTCCGACTCCTGGGTTCAAGCAATTCTTCTGCCTCAGCCTCCTGAGTAGC TCGGCTCACTGCAACCTCCGACTCCTGGGTTCCAGCAATTCTTCTGCCTCAGCCTCCTGAGTAGC A C APOLD1 Ensembl:ENSG00000178878 Protein coding intron GSE100210 HepG2 cell line chr12:12790103..12790104 29129909 RNA-Seq:(High) rs536960275 Functional Loss SNV ICGC 33..33 33 PBCA 1 - 54557 RMVar_ID_54557 Human_SNP_ID_814146827 A-to-I Human chr12 - 92531167 92531167 92531167 CATTGGGGAGTAAAGAGGGCATCCACCAGCAAAACCACAGTTGTTGACAGCCATAAGATTAGAGA CATTGGGGAGTAAAGAGGGCATCCACCAGCAAGACCACAGTTGTTGACAGCCATAAGATTAGAGA T C - - Other Unknown GSE100210 HepG2 cell line chr12:92531166..92531167 29129909 RNA-Seq:(High) rs943310682 Functional Loss SNV ICGC 33..33 33 LICA 1 - 54558 RMVar_ID_54558 Human_SNP_ID_814150853 A-to-I Human chr12 + 112130165 112130165 112130165 TTTTTTTTTGTATTTTTTGTAGACATGACGTTACCCCATGTTGTGGCCAGGTTGGTCTTAAACTC TTTTTTTTTGTATTTTTTGTAGACATGACGTTCCCCCATGTTGTGGCCAGGTTGGTCTTAAACTC A C TRAFD1 Ensembl:ENSG00000135148 Protein coding intron GSE100210 HepG2 cell line chr12:112130164..112130165 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 54559 RMVar_ID_54559 Human_SNP_ID_814159810 A-to-I Human chr12 + 21447798 21447798 21447798 CACGAGGTCAGGAGGTCGAGACCGTCCTGGCTAACACGGTGAAATCCCGTCTCTACTAAAAATAC CACGAGGTCAGGAGGTCGAGACCGTCCTGGCTGACACGGTGAAATCCCGTCTCTACTAAAAATAC A G PYROXD1 Ensembl:ENSG00000121350 Protein coding intron GSE100210 HepG2 cell line chr12:21447798..21447799 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 3 pancreas RMVar_hsa_circ_27383,RMVar_hsa_circ_48181,RMVar_hsa_circ_69061 54560 RMVar_ID_54560 Human_SNP_ID_814189657 A-to-I Human chr12 - 121243884 121243884 121243884 GGGACCCCACTGCCCTTCCCACTGAGCACATCATGGCTACCTGACTTGGTGGGAGCTCCAGGCAG GGGACCCCACTGCCCTTCCCACTGAGCACATCGTGGCTACCTGACTTGGTGGGAGCTCCAGGCAG T C CAMKK2 Ensembl:ENSG00000110931 Protein coding intron GSE38233 cultured B-cells chr12:121243883..121243884 24183664 RNA-Seq:(High) rs1063843 Functional Loss SNV ICGC 33..33 33 LAML 1 - GWAS_ID_3924,GWAS_ID_3925,GWAS_ID_3926,GWAS_ID_3927,GWAS_ID_3928,GWAS_ID_3929,GWAS_ID_3930,GWAS_ID_3931,GWAS_ID_3932,GWAS_ID_3933,GWAS_ID_3934,GWAS_ID_3935,GWAS_ID_3936,GWAS_ID_3937,GWAS_ID_3938,GWAS_ID_3939,GWAS_ID_3940,GWAS_ID_3941,GWAS_ID_3942,GWAS_ID_3943,GWAS_ID_3944,GWAS_ID_3945 RMVar_hsa_circ_119675,RMVar_hsa_circ_160875 54561 RMVar_ID_54561 Human_SNP_ID_814190885 A-to-I Human chr12 + 4569661 4569661 4569661 AAAAAATTTGAAAGTAGAGACAGGGTCTCGCTATGTTGCCCAGGCTGGTCTCAAACTCCTGGGCT AAAAAATTTGAAAGTAGAGACAGGGTCTCGCTGTGTTGCCCAGGCTGGTCTCAAACTCCTGGGCT A G DYRK4 Ensembl:ENSG00000010219 Protein coding intron GSE100210 HepG2 cell line chr12:4569660..4569661 29129909 RNA-Seq:(High) rs1193639593 Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_65281,RMVar_hsa_circ_364808 54562 RMVar_ID_54562 Human_SNP_ID_814231018 A-to-I Human chr12 - 123412340 123412340 123412340 GCCCAGGAGTTCGAGACCAGCCTAGGCAACATAGTAAGAACCTATCTTTACAAAAAACAAAAAAT GCCCAGGAGTTCGAGACCAGCCTAGGCAACATCGTAAGAACCTATCTTTACAAAAAACAAAAAAT T G RILPL2 Ensembl:ENSG00000150977 Protein coding 3'UTR GSE38233 cultured B-cells chr12:123412339..123412340 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 2 oesophagus 54563 RMVar_ID_54563 Human_SNP_ID_814236736 A-to-I Human chr12 + 64449012 64449012 64449012 CTTGAGGTCAGGAGTTCGAGACTAGCCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATAC CTTGAGGTCAGGAGTTCGAGACTAGCCTGGCCGACATGGTGAAACCCCATCTCTACTAAAAATAC A G XPOT Ensembl:ENSG00000184575 Protein coding 3'UTR GSE38233;GSE107867 cultured B-cells;ASD brains,Fragile X samples from NIH NeuroBioBank chr12:64449011..64449012;chr12:64449012..64449013 24183664,30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 54564 RMVar_ID_54564 Human_SNP_ID_814237347 A-to-I Human chr12 - 48928591 48928591 48928591 CCTGTAGTCCCAGCTACTCTGGAGGCTGAAACAGGAGAATTGCCTGAACCTGGGAGGTGGAGGCT CCTGTAGTCCCAGCTACTCTGGAGGCTGAAACTGGAGAATTGCCTGAACCTGGGAGGTGGAGGCT T A AC073610.2 Ensembl:ENSG00000272822 Protein coding intron GSE100210 HepG2 cell line chr12:48928590..48928591 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 3 prostate Human_RBP_ID_9687079,Human_RBP_ID_11953032,Human_RBP_ID_24973505 54565 RMVar_ID_54565 Human_SNP_ID_814277034 A-to-I Human chr12 - 51384462 51384462 51384462 GTCTTGAACTCCTGGCCTAAAGTGATCTGCCCACCATGGCCTCCCAAAGTGCTGGGATTTCAGGT GTCTTGAACTCCTGGCCTAAAGTGATCTGCCCGCCATGGCCTCCCAAAGTGCTGGGATTTCAGGT T C GALNT6 Ensembl:ENSG00000139629 Protein coding intron GSE100210 HepG2 cell line chr12:51384461..51384462 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 54566 RMVar_ID_54566 Human_SNP_ID_814277038 A-to-I Human chr12 - 51384462 51384462 51384462 GTCTTGAACTCCTGGCCTAAAGTGATCTGCCCACCATGGCCTCCCAAAGTGCTGGGATTTCAGGT GTCTTGAACTCCTGGCCTAAAGTGATCTGCCCCCCATGGCCTCCCAAAGTGCTGGGATTTCAGGT T G GALNT6 Ensembl:ENSG00000139629 Protein coding intron GSE100210 HepG2 cell line chr12:51384461..51384462 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 54567 RMVar_ID_54567 Human_SNP_ID_814294512 A-to-I Human chr12 - 98455399 98455399 98455399 ACAATGACAGCTTTCAAGTCTTACAAGGGGACAGCCCAGATTCTGCCAGAGGAAACTGGACAAAA ACAATGACAGCTTTCAAGTCTTACAAGGGGACGGCCCAGATTCTGCCAGAGGAAACTGGACAAAA T C SLC9A7P1 Ensembl:ENSG00000227825 Pseudogene exon GSE107867 ASD brains,frontal_cortex chr12:98455398..98455399 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_5556521,Human_RBP_ID_8248056 54568 RMVar_ID_54568 Human_SNP_ID_814298538 A-to-I Human chr12 - 56297559 56297559 56297559 GCTGGGGTTAGCAGGTGTGCACCACCACGCCCAGCTAATTTTTTGTATTTTTGGTAGAGACGGGG GCTGGGGTTAGCAGGTGTGCACCACCACGCCCGGCTAATTTTTTGTATTTTTGGTAGAGACGGGG T C CS,AC073896.1 Ensembl:ENSG00000062485,Ensembl:ENSG00000144785 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells chr12:56297558..56297559 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_83353,RMVar_hsa_circ_92622,RMVar_hsa_circ_157328,RMVar_hsa_circ_157335,RMVar_hsa_circ_365232,RMVar_hsa_circ_361093,RMVar_hsa_circ_335439 54569 RMVar_ID_54569 Human_SNP_ID_814300465 A-to-I Human chr12 + 64448979 64448979 64448979 CCAGAACTTTGGGAGGCCAAGGCAGGTGGATCACTTGAGGTCAGGAGTTCGAGACTAGCCTGGCC CCAGAACTTTGGGAGGCCAAGGCAGGTGGATCGCTTGAGGTCAGGAGTTCGAGACTAGCCTGGCC A G XPOT Ensembl:ENSG00000184575 Protein coding 3'UTR GSE100210 HepG2 cell line chr12:64448978..64448979 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 54570 RMVar_ID_54570 Human_SNP_ID_814344417 A-to-I Human chr12 + 62965545 62965545 62965545 GTTTCCGCACAGTGCCCGCCAAAAGTATGTCCAACAAGCCTGGCAGAAGGCAGACATCAATACAA GTTTCCGCACAGTGCCCGCCAAAAGTATGTCCGACAAGCCTGGCAGAAGGCAGACATCAATACAA A G RPL14P1 Ensembl:ENSG00000139239 Pseudogene exon GSE100210 HepG2 cell line chr12:62965544..62965545 29129909 RNA-Seq:(High) rs879234821 Functional Loss SNV TCGA,ICGC 33..33 33 STAD 2 - RMVar_hsa_circ_123760,RMVar_hsa_circ_157846 54571 RMVar_ID_54571 Human_SNP_ID_814350776 A-to-I Human chr12 + 110472891 110472891 110472891 CCAGCTACCTGGGAGGCTGAGGTGGGAGAATCACTTGAAACTGGGAGGCAGAGGTTCCAATGACC CCAGCTACCTGGGAGGCTGAGGTGGGAGAATCGCTTGAAACTGGGAGGCAGAGGTTCCAATGACC A G FAM216A Ensembl:ENSG00000204856 Protein coding intron GSE38233 cultured B-cells chr12:110472890..110472891 24183664 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 1 large intestine RMVar_hsa_circ_159862,RMVar_hsa_circ_106783 54572 RMVar_ID_54572 Human_SNP_ID_814363503 A-to-I Human chr12 - 102099131 102099131 102099131 TGTTTGATCCCAAAGAAGGCCAAGAAATTGCAAGTGTGAGTGACGATCACACCTGCAGGTATGTT TGTTTGATCCCAAAGAAGGCCAAGAAATTGCACGTGTGAGTGACGATCACACCTGCAGGTATGTT T G NUP37 Ensembl:ENSG00000075188 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector chr12:102099130..102099131 29967493 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 HNSC,head_neck squamous_cell_carcinoma 4 head and neck Human_RBP_ID_3942024,Human_RBP_ID_8362860,Human_RBP_ID_22436091,Human_RBP_ID_22756094,Human_RBP_ID_26899793 Human_Splice_Rec_1415196,Human_Splice_Rec_1415197,Human_Splice_Rec_1415216,Human_Splice_Rec_1415217,Human_Splice_Rec_1415244,Human_Splice_Rec_1415245,Human_Splice_Rec_1415258,Human_Splice_Rec_1415259,Human_Splice_Rec_1415270,Human_Splice_Rec_1415271 RMVar_hsa_circ_118881,RMVar_hsa_circ_159329,RMVar_hsa_circ_52145,RMVar_hsa_circ_159328,RMVar_hsa_circ_294893,RMVar_hsa_circ_348313,RMVar_hsa_circ_363764,RMVar_hsa_circ_377766,RMVar_hsa_circ_344046,RMVar_hsa_circ_159330 54573 RMVar_ID_54573 Human_SNP_ID_814385760 A-to-I Human chr12 + 117029793 117029793 117029793 TACCACAACTGGCTAATTTTTACATTTTTAGTAGAGACGGGGGATATTGCTATGTTGGCCAGGCT TACCACAACTGGCTAATTTTTACATTTTTAGTGGAGACGGGGGATATTGCTATGTTGGCCAGGCT A G FBXW8 Ensembl:ENSG00000174989 Protein coding 3'UTR GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line chr12:117029792..117029793 24183664,29129909,29796672,31158229,32596459 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BOCA 1 - 54574 RMVar_ID_54574 Human_SNP_ID_814450939 A-to-I Human chr12 - 110456862 110456862 110456862 GAGACCCTGTCTCTACAAAAAATATAAAAATTAGCTAGACGTTGTGGCACATGCCTGTAGTCCCA GAGACCCTGTCTCTACAAAAAATATAAAAATTCGCTAGACGTTGTGGCACATGCCTGTAGTCCCA T G GPN3 Ensembl:ENSG00000111231 Protein coding intron GSE38233 cultured B-cells chr12:110456861..110456862 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - RMVar_hsa_circ_159860,RMVar_hsa_circ_284114,RMVar_hsa_circ_318080,RMVar_hsa_circ_159861 54575 RMVar_ID_54575 Human_SNP_ID_814462116 A-to-I Human chr12 - 55807407 55807407 55807407 CCTTGGCCTCACAAGGGGCTGGAATTGTAAGCATAAGCCACCAAGATCAAGATTGTTACTTAATA CCTTGGCCTCACAAGGGGCTGGAATTGTAAGCGTAAGCCACCAAGATCAAGATTGTTACTTAATA T C AC023055.1,SARNP Ensembl:ENSG00000257390,Ensembl:ENSG00000205323 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells chr12:55807406..55807407 24183664 RNA-Seq:(High) rs7954839 Functional Loss SNV ICGC 33..33 33 LAML 1 - RMVar_hsa_circ_157120,RMVar_hsa_circ_127815,RMVar_hsa_circ_157122 54576 RMVar_ID_54576 Human_SNP_ID_814527824 A-to-I Human chr12 + 92859154 92859154 92859154 ACTAGAGATTATAAAGAAGAATTTTGATCTCCACCCTAGGGTCATTGTCAGGGATCTGGATCTGA ACTAGAGATTATAAAGAAGAATTTTGATCTCCGCCCTAGGGTCATTGTCAGGGATCTGGATCTGA A G AC026111.1 Ensembl:ENSG00000258012 Pseudogene exon GSE100210 HepG2 cell line chr12:92859153..92859154 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue Human_miRNA_ID_1821192,Human_miRNA_ID_1898509 54577 RMVar_ID_54577 Human_SNP_ID_814534476 A-to-I Human chr12 - 95002762 95002762 95002762 AGTGGGGGAAGACAAATATGGAAACAAATACTATGAAGACAACAAGCAATTTTTTGGTGAGTGCA AGTGGGGGAAGACAAATATGGAAACAAATACTGTGAAGACAACAAGCAATTTTTTGGTGAGTGCA T C NDUFA12 Ensembl:ENSG00000184752 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector chr12:95002761..95002762 29967493 RNA-Seq:(High) rs766118227 Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,UCEC,endometrium endometrioid_carcinoma 8 lung,uterus Human_RBP_ID_1803201,Human_RBP_ID_3417162,Human_RBP_ID_17241928,Human_RBP_ID_17650807,Human_RBP_ID_18526834,Human_RBP_ID_19058840,Human_RBP_ID_27635103 Human_Splice_Rec_1408224,Human_Splice_Rec_1408225,Human_Splice_Rec_1408240,Human_Splice_Rec_1408246,Human_Splice_Rec_1408247,Human_Splice_Rec_1408254,Human_Splice_Rec_1408255,Human_Splice_Rec_1408260,Human_Splice_Rec_1408261,Human_Splice_Rec_1408264,Human_Splice_Rec_1408265 RMVar_hsa_circ_83213,RMVar_hsa_circ_111874,RMVar_hsa_circ_158821,RMVar_hsa_circ_158822 54578 RMVar_ID_54578 Human_SNP_ID_814539914 A-to-I Human chr12 + 45174536 45174536 45174536 ATACTGTTCCCCGGGGATTATCAGGTCCATGCATGTATTATCTACAGAATGAACTTCAATTTCAC ATACTGTTCCCCGGGGATTATCAGGTCCATGCGTGTATTATCTACAGAATGAACTTCAATTTCAC A G - - Other Unknown GSE100210 HepG2 cell line chr12:45174535..45174536 29129909 RNA-Seq:(High) rs913431289 Functional Loss SNV ICGC 33..33 33 LAML 1 - 54579 RMVar_ID_54579 Human_SNP_ID_814562873 A-to-I Human chr12 + 53427673 53427673 53427673 GATCTGCCTGCCTCGGCCTCCCAAAGTGCTGGAATTACAGGCGTGAGCCACCCCGCCCGGCCATG GATCTGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCCCGCCCGGCCATG A G AMHR2 Ensembl:ENSG00000135409 Protein coding intron GSE47997 K562 cells&HepG2 cells chr12:53427672..53427673;chr12:53427673..53427674 23474544 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 3 prostate 54580 RMVar_ID_54580 Human_SNP_ID_814589915 A-to-I Human chr12 - 111933038 111933038 111933038 CAGGGTTTCGCCATGTTGGCCAGGCTGGTCTCAACCTCCTGACCTCAGGTGATCTGCCCACCTTG CAGGGTTTCGCCATGTTGGCCAGGCTGGTCTCGACCTCCTGACCTCAGGTGATCTGCCCACCTTG T C TMEM116 Ensembl:ENSG00000198270 Protein coding intron GSE100210 HepG2 cell line chr12:111933037..111933038 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 STAD 1 - RMVar_hsa_circ_160067,RMVar_hsa_circ_160068,RMVar_hsa_circ_160072,RMVar_hsa_circ_100434,RMVar_hsa_circ_160069,RMVar_hsa_circ_160070,RMVar_hsa_circ_288508,RMVar_hsa_circ_293964,RMVar_hsa_circ_299054,RMVar_hsa_circ_266501,RMVar_hsa_circ_160074,RMVar_hsa_circ_160075,RMVar_hsa_circ_160073,RMVar_hsa_circ_160071 54581 RMVar_ID_54581 Human_SNP_ID_814599186 A-to-I Human chr12 - 31510974 31510974 31510974 CCCCCGCCTTGACCTCCCAAAATGTTAGGATTACAGGCATGAGCCACCACACCCAGCCCTGAGTA CCCCCGCCTTGACCTCCCAAAATGTTAGGATTGCAGGCATGAGCCACCACACCCAGCCCTGAGTA T C DENND5B Ensembl:ENSG00000170456 Protein coding intron GSE100210 HepG2 cell line chr12:31510973..31510974 29129909 RNA-Seq:(High) rs1043419854 Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_89244,RMVar_hsa_circ_155707 54582 RMVar_ID_54582 Human_SNP_ID_814600413 A-to-I Human chr12 - 93436772 93436772 93436772 TTATCTTCTGGACCAAAGCTCTTTTAGCCAATAAAAGTGACTGAAGCTGGGCATGGTGGTTCACA TTATCTTCTGGACCAAAGCTCTTTTAGCCAATCAAAGTGACTGAAGCTGGGCATGGTGGTTCACA T G UBE2N Ensembl:ENSG00000177889 Protein coding intron GSE100210 HepG2 cell line chr12:93436771..93436772 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_12056190,Human_RBP_ID_19817762 54583 RMVar_ID_54583 Human_SNP_ID_814622099 A-to-I Human chr12 - 123158873 123158873 123158873 TAATCTCAGCACTTTGGGAGGCCAAGGTGGGCAGATCACTTGAGGTCAGGAGTTTGAGGCCGGCC TAATCTCAGCACTTTGGGAGGCCAAGGTGGGCGGATCACTTGAGGTCAGGAGTTTGAGGCCGGCC T C MPHOSPH9 Ensembl:ENSG00000051825 Protein coding intron GSE38233 cultured B-cells chr12:123158872..123158873 24183664 RNA-Seq:(High) rs2695481 Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_81544,RMVar_hsa_circ_98333,RMVar_hsa_circ_161237,RMVar_hsa_circ_161238 54584 RMVar_ID_54584 Human_SNP_ID_814686752 A-to-I Human chr12 + 62559482 62559482 62559482 ATGGGCAACATGGTGAAACCCTATCTCTACAAAAAATACAAAAATTAGCCAAGTGTGGTGGTGTG ATGGGCAACATGGTGAAACCCTATCTCTACAAGAAATACAAAAATTAGCCAAGTGTGGTGGTGTG A G MON2 Ensembl:ENSG00000061987 Protein coding intron GSE47997 K562 cells&HepG2 cells chr12:62559482..62559483 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - Human_RBP_ID_12000979 RMVar_hsa_circ_18305,RMVar_hsa_circ_95869,RMVar_hsa_circ_157814,RMVar_hsa_circ_51539,RMVar_hsa_circ_157818,RMVar_hsa_circ_81252,RMVar_hsa_circ_157823,RMVar_hsa_circ_45007,RMVar_hsa_circ_48200,RMVar_hsa_circ_56832,RMVar_hsa_circ_57783,RMVar_hsa_circ_58103,RMVar_hsa_circ_285588,RMVar_hsa_circ_157835,RMVar_hsa_circ_338553,RMVar_hsa_circ_157838,RMVar_hsa_circ_16390,RMVar_hsa_circ_75028,RMVar_hsa_circ_331877,RMVar_hsa_circ_266032,RMVar_hsa_circ_51588 54585 RMVar_ID_54585 Human_SNP_ID_814697947 A-to-I Human chr12 + 68830728 68830728 68830728 ATTATACCCTATTTATTTATTTATTGAGATTGAGTCTCTCTGTCTCCCAGGCTGGAGTGCAGTGG ATTATACCCTATTTATTTATTTATTGAGATTGGGTCTCTCTGTCTCCCAGGCTGGAGTGCAGTGG A G MDM2 Ensembl:ENSG00000135679 Protein coding intron GSE100210 HepG2 cell line chr12:68830727..68830728 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 16 liver RMVar_hsa_circ_3503,RMVar_hsa_circ_118742,RMVar_hsa_circ_38758,RMVar_hsa_circ_158126,RMVar_hsa_circ_28606,RMVar_hsa_circ_360939,RMVar_hsa_circ_36682,RMVar_hsa_circ_268768,RMVar_hsa_circ_285716,RMVar_hsa_circ_158135,RMVar_hsa_circ_158136 54586 RMVar_ID_54586 Human_SNP_ID_814771266 A-to-I Human chr12 + 64448989 64448989 64448989 GGGAGGCCAAGGCAGGTGGATCACTTGAGGTCAGGAGTTCGAGACTAGCCTGGCCAACATGGTGA GGGAGGCCAAGGCAGGTGGATCACTTGAGGTCGGGAGTTCGAGACTAGCCTGGCCAACATGGTGA A G XPOT Ensembl:ENSG00000184575 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line chr12:64448988..64448989 24183664,31158229,31158229 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 54587 RMVar_ID_54587 Human_SNP_ID_814780935 A-to-I Human chr12 + 113391148 113391147 113391148 CCTAAGCCATATTGTGGTATACAGACAGATACAAAAAAAAAGGCTCTCTCCCTGTCTGATCTCAT CCTAAGCCATATTGTGGTATACAGACAGATAC_AAAAAAAAGGCTCTCTCCCTGTCTGATCTCAT CA C PLBD2 Ensembl:ENSG00000151176 Protein coding 3'UTR GSE100210 HepG2 cell line chr12:113391148..113391149 29129909 RNA-Seq:(High) rs201259647 Functional Loss DEL ICGC 33..33 33 CHOL 1 - Human_RBP_ID_194985,Human_RBP_ID_259934,Human_RBP_ID_2306617,Human_RBP_ID_17075372,Human_RBP_ID_17561286,Human_RBP_ID_22369790,Human_RBP_ID_24530000,Human_RBP_ID_26412228,Human_RBP_ID_26755649 54588 RMVar_ID_54588 Human_SNP_ID_814825531 A-to-I Human chr12 - 42432566 42432566 42432566 GGAATTTGTGGAGGATTTTATTCAGGTTTCTAAGAATCTCACTGGAAAAGTAATTGGAAAAAATG GGAATTTGTGGAGGATTTTATTCAGGTTTCTAGGAATCTCACTGGAAAAGTAATTGGAAAAAATG T C AC079601.3 Ensembl:ENSG00000257376 Pseudogene intron GSE100210 HepG2 cell line chr12:42432565..42432566 29129909 RNA-Seq:(High) rs531918527 Functional Loss SNV ICGC 33..33 33 LUSC 1 - 54589 RMVar_ID_54589 Human_SNP_ID_814895097 A-to-I Human chr12 + 101747075 101747075 101747075 CTGGATATTTTCCTTCTTCGGGCCAAACTGCTAAGCATCACATCACAAAGACATCTCTGTGAAGC CTGGATATTTTCCTTCTTCGGGCCAAACTGCTGAGCATCACATCACAAAGACATCTCTGTGAAGC A G NONHSAG012082.2 RNACentral:URS00009B616C lincRNA intron GSE100210 HepG2 cell line chr12:101747075..101747076 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_11780379 54590 RMVar_ID_54590 Human_SNP_ID_814898596 A-to-I Human chr12 + 107697836 107697836 107697836 TGTTCTTTCTTACACAAAACTAGTTCAAAGCTAGTATATTAATATGAATAGCTACTATAGATGAA TGTTCTTTCTTACACAAAACTAGTTCAAAGCTGGTATATTAATATGAATAGCTACTATAGATGAA A G PWP1 Ensembl:ENSG00000136045 Protein coding intron GSE100210 HepG2 cell line chr12:107697835..107697836 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 haematopoietic and lymphoid tissue RMVar_hsa_circ_114180,RMVar_hsa_circ_317567,RMVar_hsa_circ_287745,RMVar_hsa_circ_159585 54591 RMVar_ID_54591 Human_SNP_ID_814999226 A-to-I Human chr12 + 9659572 9659572 9659572 GGCATGTGCCACCACACCTGGCTAATTTTTGTATTTTTAGTAGAGATTGGGTTTTGCCGTGTGGG GGCATGTGCCACCACACCTGGCTAATTTTTGTGTTTTTAGTAGAGATTGGGTTTTGCCGTGTGGG A G AC010186.3 Ensembl:ENSG00000257027 lincRNA intron GSE38233 cultured B-cells chr12:9659571..9659572 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - RMVar_hsa_circ_154848 54592 RMVar_ID_54592 Human_SNP_ID_815002843 A-to-I Human chr12 - 54182609 54182609 54182609 CTCTCTCCTTCCTCACAGGTGCCCTTTGGGGAAGTAAGCATGGTCCGGGACTGGTTGGGCATTGT CTCTCTCCTTCCTCACAGGTGCCCTTTGGGGACGTAAGCATGGTCCGGGACTGGTTGGGCATTGT T G SMUG1 Ensembl:ENSG00000123415 Protein coding intron GSE112787 293 Flip-In T-REx cells,empty vector chr12:54182608..54182609 29967493 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 LIHC,liver hepatocellular_carcinoma 11 liver Human_RBP_ID_877047,Human_RBP_ID_25016955,Human_RBP_ID_26422303 Human_Splice_Rec_1376834,Human_Splice_Rec_1376846,Human_Splice_Rec_1376860,Human_Splice_Rec_1376866,Human_Splice_Rec_1376872,Human_Splice_Rec_1376880,Human_Splice_Rec_1376892,Human_Splice_Rec_1376896,Human_Splice_Rec_1376902,Human_Splice_Rec_1376906,Human_Splice_Rec_1376910,Human_Splice_Rec_1376914,Human_Splice_Rec_1376922,Human_Splice_Rec_1376924,Human_Splice_Rec_1376930 RMVar_hsa_circ_352229,RMVar_hsa_circ_66280,RMVar_hsa_circ_104034,RMVar_hsa_circ_276429,RMVar_hsa_circ_157009,RMVar_hsa_circ_330801 54593 RMVar_ID_54593 Human_SNP_ID_815039305 A-to-I Human chr12 - 92858395 92858395 92858395 TCTGGTGACTGTTGCTCCAAGGCTACCAGCACATTACAAGTCTTGTAGTCAAACCCTTTGGAAGA TCTGGTGACTGTTGCTCCAAGGCTACCAGCACGTTACAAGTCTTGTAGTCAAACCCTTTGGAAGA T C EEA1 Ensembl:ENSG00000102189 Protein coding intron GSE38233 cultured B-cells chr12:92858394..92858395 24183664 RNA-Seq:(High) rs879175631 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue RMVar_hsa_circ_4291,RMVar_hsa_circ_54091,RMVar_hsa_circ_73433,RMVar_hsa_circ_26898,RMVar_hsa_circ_58505,RMVar_hsa_circ_348148,RMVar_hsa_circ_60946,RMVar_hsa_circ_367556,RMVar_hsa_circ_309256,RMVar_hsa_circ_73196 54594 RMVar_ID_54594 Human_SNP_ID_815064484 A-to-I Human chr12 + 42432570 42432570 42432570 TTTTCCAATTACTTTTCCAGTGAGATTCTTAGAAACCTGAATAAAATCCTCCACAAATTCCAAGA TTTTCCAATTACTTTTCCAGTGAGATTCTTAGGAACCTGAATAAAATCCTCCACAAATTCCAAGA A G PPHLN1 Ensembl:ENSG00000134283 Protein coding intron GSE100210 HepG2 cell line chr12:42432569..42432570 29129909 RNA-Seq:(High) rs549890660 Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_3404614,Human_RBP_ID_8375017 RMVar_hsa_circ_109108,RMVar_hsa_circ_155950 54595 RMVar_ID_54595 Human_SNP_ID_815081063 A-to-I Human chr12 + 131938302 131938302 131938302 CCTGTCTCTACAAAAAAAATTGAAAACTAGCCAGGCATCGTGGTGCCTGTCTGTAGTCTCAGCTA CCTGTCTCTACAAAAAAAATTGAAAACTAGCCTGGCATCGTGGTGCCTGTCTGTAGTCTCAGCTA A T PUS1 Ensembl:ENSG00000177192 Protein coding intron GSE100210 HepG2 cell line chr12:131938301..131938302 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_24949296 RMVar_hsa_circ_15521,RMVar_hsa_circ_110077,RMVar_hsa_circ_51260,RMVar_hsa_circ_114954,RMVar_hsa_circ_161750,RMVar_hsa_circ_161751 54596 RMVar_ID_54596 Human_SNP_ID_815138451 A-to-I Human chr12 + 32700223 32700223 32700223 CTTACTGCAACCTCCACCTCCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGG CTTACTGCAACCTCCACCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTGAGTAGCTGGG A G DNM1L Ensembl:ENSG00000087470 Protein coding intron GSE100210 HepG2 cell line chr12:32700223..32700224 29129909 RNA-Seq:(High) rs7968325 Functional Loss SNV ICGC 33..33 33 ESCA 1 - 54597 RMVar_ID_54597 Human_SNP_ID_815159587 A-to-I Human chr12 + 7607036 7607036 7607036 GAAAGTATCCGTAAATGGAGAGAAGAGCAAACAGAACGCTTGGAAGCCCTTGATGCCAATTCTCA GAAAGTATCCGTAAATGGAGAGAAGAGCAAACGGAACGCTTGGAAGCCCTTGATGCCAATTCTCA A G AC006927.1 Ensembl:ENSG00000255977 Pseudogene exon GSE100210 HepG2 cell line chr12:7607035..7607036 29129909 RNA-Seq:(High) rs879063602 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_23575580 54598 RMVar_ID_54598 Human_SNP_ID_815212980 A-to-I Human chr12 - 110380337 110380337 110380337 ATTTTTTTTATTTTTATTTGAGATAGAGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGTGCA ATTTTTTTTATTTTTATTTGAGATAGAGTCTCGCTCTGTCACCCAGGCTGGAGTGCAGTGGTGCA T C ANAPC7 Ensembl:ENSG00000196510 Protein coding intron GSE38233 cultured B-cells chr12:110380336..110380337 24183664 RNA-Seq:(High) rs1351029693 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue 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 54599 RMVar_ID_54599 Human_SNP_ID_815236668 A-to-I Human chr12 + 62965533 62965532 62965533 TTTCATCCTCAAGTTTCCGCACAGTGCCCGCCAAAAGTATGTCCAACAAGCCTGGCAGAAGGCAG TTTCATCCTCAAGTTTCCGCACAGTGCCCGCC_AAAGTATGTCCAACAAGCCTGGCAGAAGGCAG CA C RPL14P1 Ensembl:ENSG00000139239 Pseudogene exon GSE100210 HepG2 cell line chr12:62965533..62965534 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 33..33 33 LICA 1 - Human_RBP_ID_18527010 RMVar_hsa_circ_123760,RMVar_hsa_circ_157846 54600 RMVar_ID_54600 Human_SNP_ID_815250234 A-to-I Human chr12 - 38701561 38701561 38701561 TGAACCCAAGAGGTAGAGGTTACAGTGAGCCAAGATTGTGCCACTGTACTCCAAACTGGGTGACA TGAACCCAAGAGGTAGAGGTTACAGTGAGCCACGATTGTGCCACTGTACTCCAAACTGGGTGACA T G CPNE8 Ensembl:ENSG00000139117 Protein coding intron GSE100210 HepG2 cell line chr12:38701560..38701561 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_55517,RMVar_hsa_circ_81350,RMVar_hsa_circ_155817,RMVar_hsa_circ_315347,RMVar_hsa_circ_46640,RMVar_hsa_circ_63387,RMVar_hsa_circ_30891,RMVar_hsa_circ_114994,RMVar_hsa_circ_155818,RMVar_hsa_circ_286546,RMVar_hsa_circ_348709,RMVar_hsa_circ_155819,RMVar_hsa_circ_322594,RMVar_hsa_circ_108827,RMVar_hsa_circ_70867,RMVar_hsa_circ_155821,RMVar_hsa_circ_155822,RMVar_hsa_circ_155820,RMVar_hsa_circ_66735,RMVar_hsa_circ_11593,RMVar_hsa_circ_43889,RMVar_hsa_circ_333229,RMVar_hsa_circ_337465,RMVar_hsa_circ_350943,RMVar_hsa_circ_286241,RMVar_hsa_circ_155824,RMVar_hsa_circ_155825,RMVar_hsa_circ_155823 54601 RMVar_ID_54601 Human_SNP_ID_815267582 A-to-I Human chr12 - 26990568 26990568 26990568 ACAAGTGTTTCCTTCTCCTCCCTCCCGGGACAAGGTGTCATATACAATGTCATTGTTTGGGACCC ACAAGTGTTTCCTTCTCCTCCCTCCCGGGACACGGTGTCATATACAATGTCATTGTTTGGGACCC T G TM7SF3 Ensembl:ENSG00000064115 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector chr12:26990567..26990568 29967493 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 READ 1 - Human_RBP_ID_417411,Human_RBP_ID_27627351 Human_Splice_Rec_1349258,Human_Splice_Rec_1349284,Human_Splice_Rec_1349296,Human_Splice_Rec_1349312,Human_Splice_Rec_1349334,Human_Splice_Rec_1349342 Human_miRNA_ID_2599744 RMVar_hsa_circ_155432,RMVar_hsa_circ_91077,RMVar_hsa_circ_123334,RMVar_hsa_circ_155433,RMVar_hsa_circ_155436,RMVar_hsa_circ_266379,RMVar_hsa_circ_304304,RMVar_hsa_circ_51618,RMVar_hsa_circ_378029,RMVar_hsa_circ_317415,RMVar_hsa_circ_278776,RMVar_hsa_circ_107534,RMVar_hsa_circ_155443,RMVar_hsa_circ_31992,RMVar_hsa_circ_155444,RMVar_hsa_circ_155445,RMVar_hsa_circ_155441,RMVar_hsa_circ_155442,RMVar_hsa_circ_65150,RMVar_hsa_circ_309042,RMVar_hsa_circ_292564,RMVar_hsa_circ_155453,RMVar_hsa_circ_155449,RMVar_hsa_circ_276377,RMVar_hsa_circ_155446,RMVar_hsa_circ_155447,RMVar_hsa_circ_311457,RMVar_hsa_circ_313336,RMVar_hsa_circ_316275,RMVar_hsa_circ_281133,RMVar_hsa_circ_155451,RMVar_hsa_circ_155450,RMVar_hsa_circ_273732,RMVar_hsa_circ_285081,RMVar_hsa_circ_314822,RMVar_hsa_circ_155448,RMVar_hsa_circ_286990,RMVar_hsa_circ_275962,RMVar_hsa_circ_155455,RMVar_hsa_circ_155456,RMVar_hsa_circ_155454,RMVar_hsa_circ_155452 54602 RMVar_ID_54602 Human_SNP_ID_815271588 A-to-I Human chr12 - 55986905 55986905 55986905 GGGTGGAGGGAGGGGGATACTGTAAAGGGGGGAGGGGGAAGGGGAGGGGATTTCCAGGCTTCAAC GGGTGGAGGGAGGGGGATACTGTAAAGGGGGGGGGGGGAAGGGGAGGGGATTTCCAGGCTTCAAC T C - - Other Unknown GSE38233 cultured B-cells chr12:55986904..55986905 24183664 RNA-Seq:(High) rs370178643 Functional Loss SNV ICGC,COSMIC 33..33 33 thyroid neoplasm,face squamous_cell_carcinoma,oesophagus squamous_cell_carcinoma,ESCA,skin squamous_cell_carcinoma 16 oesophagus,skin,head and neck 54603 RMVar_ID_54603 Human_SNP_ID_815279500 A-to-I Human chr12 + 93503398 93503398 93503398 CCAATAGCAAAAACTGATTTTTTTTTTTTTTTAAAGAAAAGGTCTTGCTGTGTCGCCCAGGATGG CCAATAGCAAAAACTGATTTTTTTTTTTTTTTGAAGAAAAGGTCTTGCTGTGTCGCCCAGGATGG A G MRPL42 Ensembl:ENSG00000198015 Protein coding 3'UTR GSE100210 HepG2 cell line chr12:93503398..93503399 29129909 RNA-Seq:(High) rs1480098941 Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_430175,Human_RBP_ID_2362335,Human_RBP_ID_4244341,Human_RBP_ID_6233134,Human_RBP_ID_8179346,Human_RBP_ID_12057103,Human_RBP_ID_22384546,Human_RBP_ID_22795534,Human_RBP_ID_23159310,Human_RBP_ID_24407779,Human_RBP_ID_24468156,Human_RBP_ID_25028178,Human_RBP_ID_26421542,Human_RBP_ID_26912522 54604 RMVar_ID_54604 Human_SNP_ID_815325010 A-to-I Human chr12 + 92859159 92859159 92859159 AGATTATAAAGAAGAATTTTGATCTCCACCCTAGGGTCATTGTCAGGGATCTGGATCTGAAGAAG AGATTATAAAGAAGAATTTTGATCTCCACCCTGGGGTCATTGTCAGGGATCTGGATCTGAAGAAG A G AC026111.1 Ensembl:ENSG00000258012 Pseudogene exon GSE100210 HepG2 cell line chr12:92859158..92859159 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue Human_miRNA_ID_1903305 54605 RMVar_ID_54605 Human_SNP_ID_815338320 A-to-I Human chr12 - 64338796 64338796 64338796 AGCCTGCTGCTCACCGGCCTAGCTTTGCTCTCACCATGGCTCTCAGCAATGCTGACATGCAAAAG AGCCTGCTGCTCACCGGCCTAGCTTTGCTCTCGCCATGGCTCTCAGCAATGCTGACATGCAAAAG T C AC135279.3,C12orf56 Ensembl:ENSG00000256293,Ensembl:ENSG00000185306 Pseudogene,Protein coding exon,intron GSE100210 HepG2 cell line chr12:64338795..64338796 29129909 RNA-Seq:(High) rs879244248 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 haematopoietic and lymphoid tissue RMVar_hsa_circ_53606 54606 RMVar_ID_54606 Human_SNP_ID_815377187 A-to-I Human chr12 - 49753027 49753027 49753027 TGGACATAGGCCCCTGCAGCCGCCACAAACATACAAAGGGCAAAACTTGCATAGACCTTCTTCAG TGGACATAGGCCCCTGCAGCCGCCACAAACATGCAAAGGGCAAAACTTGCATAGACCTTCTTCAG T C - - Other Unknown GSE56152 embryonic stem cells,wild type chr12:49753026..49753027 25708366 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 54607 RMVar_ID_54607 Human_SNP_ID_815384714 A-to-I Human chr12 + 42376670 42376670 42376670 AAAATTAGCTGGGTATGGTGATGTATGCTTGTATTTTCAGCTACTCAGAAGGCTGAGGTAGGATT AAAATTAGCTGGGTATGGTGATGTATGCTTGTGTTTTCAGCTACTCAGAAGGCTGAGGTAGGATT A G PPHLN1 Ensembl:ENSG00000134283 Protein coding intron GSE100210 HepG2 cell line chr12:42376669..42376670 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_17561071 RMVar_hsa_circ_8748,RMVar_hsa_circ_155943,RMVar_hsa_circ_93526,RMVar_hsa_circ_97762,RMVar_hsa_circ_155944,RMVar_hsa_circ_355560,RMVar_hsa_circ_109108,RMVar_hsa_circ_271102,RMVar_hsa_circ_36527,RMVar_hsa_circ_23093,RMVar_hsa_circ_301317,RMVar_hsa_circ_155949,RMVar_hsa_circ_155950,RMVar_hsa_circ_319569,RMVar_hsa_circ_155952,RMVar_hsa_circ_282377,RMVar_hsa_circ_308918,RMVar_hsa_circ_367984,RMVar_hsa_circ_155951,RMVar_hsa_circ_286193,RMVar_hsa_circ_155955,RMVar_hsa_circ_155956,RMVar_hsa_circ_155954 54608 RMVar_ID_54608 Human_SNP_ID_815403145 A-to-I Human chr12 - 112222686 112222686 112222686 GGGACCACAGGTGCACACCACCATGCCCGGCTAATTTTTTGTTTGTTTTTAAAAGACAGAGTCTC GGGACCACAGGTGCACACCACCATGCCCGGCTTATTTTTTGTTTGTTTTTAAAAGACAGAGTCTC T A HECTD4 Ensembl:ENSG00000173064 Protein coding intron GSE38233 cultured B-cells chr12:112222685..112222686 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_76071,RMVar_hsa_circ_92283,RMVar_hsa_circ_86521,RMVar_hsa_circ_96738,RMVar_hsa_circ_160134,RMVar_hsa_circ_160135,RMVar_hsa_circ_160133,RMVar_hsa_circ_86374,RMVar_hsa_circ_160136,RMVar_hsa_circ_160137,RMVar_hsa_circ_160139,RMVar_hsa_circ_120037,RMVar_hsa_circ_56551,RMVar_hsa_circ_17528,RMVar_hsa_circ_78078,RMVar_hsa_circ_110981,RMVar_hsa_circ_269059,RMVar_hsa_circ_269436,RMVar_hsa_circ_120958,RMVar_hsa_circ_99564,RMVar_hsa_circ_104560,RMVar_hsa_circ_99507,RMVar_hsa_circ_82647,RMVar_hsa_circ_88433,RMVar_hsa_circ_98741,RMVar_hsa_circ_160146,RMVar_hsa_circ_160148,RMVar_hsa_circ_160150,RMVar_hsa_circ_160149,RMVar_hsa_circ_160147,RMVar_hsa_circ_160144,RMVar_hsa_circ_160145,RMVar_hsa_circ_160143,RMVar_hsa_circ_92094,RMVar_hsa_circ_160155,RMVar_hsa_circ_81719,RMVar_hsa_circ_160154,RMVar_hsa_circ_160156,RMVar_hsa_circ_22381,RMVar_hsa_circ_84481,RMVar_hsa_circ_160158,RMVar_hsa_circ_23033,RMVar_hsa_circ_347738,RMVar_hsa_circ_12086,RMVar_hsa_circ_160161,RMVar_hsa_circ_91992,RMVar_hsa_circ_326154,RMVar_hsa_circ_272179,RMVar_hsa_circ_160162,RMVar_hsa_circ_160167,RMVar_hsa_circ_84639,RMVar_hsa_circ_309283,RMVar_hsa_circ_330623,RMVar_hsa_circ_119357,RMVar_hsa_circ_160169,RMVar_hsa_circ_160170,RMVar_hsa_circ_160168,RMVar_hsa_circ_114242,RMVar_hsa_circ_344036,RMVar_hsa_circ_18248,RMVar_hsa_circ_123644,RMVar_hsa_circ_306661,RMVar_hsa_circ_160171,RMVar_hsa_circ_160177,RMVar_hsa_circ_339207,RMVar_hsa_circ_313462,RMVar_hsa_circ_116076,RMVar_hsa_circ_85907,RMVar_hsa_circ_80308,RMVar_hsa_circ_160178,RMVar_hsa_circ_160180,RMVar_hsa_circ_160181,RMVar_hsa_circ_160179,RMVar_hsa_circ_40416,RMVar_hsa_circ_269460,RMVar_hsa_circ_160184,RMVar_hsa_circ_288211,RMVar_hsa_circ_52366,RMVar_hsa_circ_160185 54609 RMVar_ID_54609 Human_SNP_ID_815408389 A-to-I Human chr12 + 66234416 66234416 66234416 GACTTTGCACCTGGTAGGCAGATACAGGAGATACAATATAGGGTGTAATAGAAGTTTGAGTGATC GACTTTGCACCTGGTAGGCAGATACAGGAGATGCAATATAGGGTGTAATAGAAGTTTGAGTGATC A G IRAK3 Ensembl:ENSG00000090376 Protein coding intron GSE100210 HepG2 cell line chr12:66234415..66234416 29129909 RNA-Seq:(High) rs1335742448 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue RMVar_hsa_circ_265450,RMVar_hsa_circ_291287,RMVar_hsa_circ_311606,RMVar_hsa_circ_157995 54610 RMVar_ID_54610 Human_SNP_ID_815416575 A-to-I Human chr12 - 118116608 118116608 118116608 CAGGCTGGAGTGCCACAGCGCGATCTCTGCTCACTACAACCTCCATCTCCCAGGCTCAAGCACTC CAGGCTGGAGTGCCACAGCGCGATCTCTGCTCGCTACAACCTCCATCTCCCAGGCTCAAGCACTC T C VSIG10 Ensembl:ENSG00000176834 Protein coding intron GSE100210 HepG2 cell line chr12:118116607..118116608 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 54611 RMVar_ID_54611 Human_SNP_ID_815426340 A-to-I Human chr12 + 68143525 68143525 68143525 ACAACTTCACACTGCTTGGCAAGCCACTCCTCAGAAAGGATCTTGTTTGAGTAGAAGCCATAGTC ACAACTTCACACTGCTTGGCAAGCCACTCCTCGGAAAGGATCTTGTTTGAGTAGAAGCCATAGTC A G AC007458.1,IFNG-AS1 Ensembl:ENSG00000256708,Ensembl:ENSG00000255733 Pseudogene,lincRNA exon,intron GSE100210 HepG2 cell line chr12:68143524..68143525 29129909 RNA-Seq:(High) rs1281102721 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_6239442 54612 RMVar_ID_54612 Human_SNP_ID_815433625 A-to-I Human chr12 - 112222449 112222449 112222449 TTGGACAGGCTGTTCTCAAACTCCTGACCTCAAGTGATCCGCCCACTTCAACCTCCCAAAGTGCT TTGGACAGGCTGTTCTCAAACTCCTGACCTCAGGTGATCCGCCCACTTCAACCTCCCAAAGTGCT T C HECTD4 Ensembl:ENSG00000173064 Protein coding intron GSE38233 cultured B-cells chr12:112222448..112222449 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 STAD 1 - RMVar_hsa_circ_76071,RMVar_hsa_circ_92283,RMVar_hsa_circ_86521,RMVar_hsa_circ_96738,RMVar_hsa_circ_160134,RMVar_hsa_circ_160135,RMVar_hsa_circ_160133,RMVar_hsa_circ_86374,RMVar_hsa_circ_160136,RMVar_hsa_circ_160137,RMVar_hsa_circ_160139,RMVar_hsa_circ_120037,RMVar_hsa_circ_56551,RMVar_hsa_circ_17528,RMVar_hsa_circ_78078,RMVar_hsa_circ_110981,RMVar_hsa_circ_269059,RMVar_hsa_circ_269436,RMVar_hsa_circ_120958,RMVar_hsa_circ_99564,RMVar_hsa_circ_104560,RMVar_hsa_circ_99507,RMVar_hsa_circ_82647,RMVar_hsa_circ_88433,RMVar_hsa_circ_98741,RMVar_hsa_circ_160146,RMVar_hsa_circ_160148,RMVar_hsa_circ_160150,RMVar_hsa_circ_160149,RMVar_hsa_circ_160147,RMVar_hsa_circ_160144,RMVar_hsa_circ_160145,RMVar_hsa_circ_160143,RMVar_hsa_circ_92094,RMVar_hsa_circ_160155,RMVar_hsa_circ_81719,RMVar_hsa_circ_160154,RMVar_hsa_circ_160156,RMVar_hsa_circ_22381,RMVar_hsa_circ_84481,RMVar_hsa_circ_160158,RMVar_hsa_circ_23033,RMVar_hsa_circ_347738,RMVar_hsa_circ_12086,RMVar_hsa_circ_160161,RMVar_hsa_circ_91992,RMVar_hsa_circ_326154,RMVar_hsa_circ_272179,RMVar_hsa_circ_160162,RMVar_hsa_circ_160167,RMVar_hsa_circ_84639,RMVar_hsa_circ_309283,RMVar_hsa_circ_330623,RMVar_hsa_circ_119357,RMVar_hsa_circ_160169,RMVar_hsa_circ_160170,RMVar_hsa_circ_160168,RMVar_hsa_circ_114242,RMVar_hsa_circ_344036,RMVar_hsa_circ_18248,RMVar_hsa_circ_123644,RMVar_hsa_circ_306661,RMVar_hsa_circ_160171,RMVar_hsa_circ_160177,RMVar_hsa_circ_339207,RMVar_hsa_circ_313462,RMVar_hsa_circ_116076,RMVar_hsa_circ_85907,RMVar_hsa_circ_80308,RMVar_hsa_circ_160178,RMVar_hsa_circ_160180,RMVar_hsa_circ_160181,RMVar_hsa_circ_160179,RMVar_hsa_circ_40416,RMVar_hsa_circ_269460,RMVar_hsa_circ_160184,RMVar_hsa_circ_288211,RMVar_hsa_circ_52366,RMVar_hsa_circ_160185 54613 RMVar_ID_54613 Human_SNP_ID_815459678 A-to-I Human chr12 - 123515716 123515716 123515716 GTTTGGCTCGGTGGCTCACACCTGTAATCCCAACACTTTGGGAGGCTGAGGCGGGCGGATCACGG GTTTGGCTCGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGCGGATCACGG T C RILPL1 Ensembl:ENSG00000188026 Protein coding intron GSE100210 HepG2 cell line chr12:123515715..123515716 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - RMVar_hsa_circ_322060,RMVar_hsa_circ_351971 54614 RMVar_ID_54614 Human_SNP_ID_815470560 A-to-I Human chr12 + 63822670 63822670 63822670 AGAATCTCTTTGGCAAGTTTGGGCCTGCCTTAAATGTGAAAGTAATGACTGGTGAAAGTGGAAAA AGAATCTCTTTGGCAAGTTTGGGCCTGCCTTACATGTGAAAGTAATGACTGGTGAAAGTGGAAAA A C PABPC1P4 Ensembl:ENSG00000255642 Pseudogene exon GSE100210 HepG2 cell line chr12:63822670..63822671 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_6239657,Human_RBP_ID_22383508 Human_miRNA_ID_1824668,Human_miRNA_ID_1845010,Human_miRNA_ID_1845479,Human_miRNA_ID_1845955 54615 RMVar_ID_54615 Human_SNP_ID_815558354 A-to-I Human chr12 + 111688139 111688139 111688139 CGCCCACTTCGGCCTCCCAAAGTGCTGGGATGACAGGCGTGAGCCACCGCGCCCGGCCCCCCCAA CGCCCACTTCGGCCTCCCAAAGTGCTGGGATGGCAGGCGTGAGCCACCGCGCCCGGCCCCCCCAA A G ACAD10 Ensembl:ENSG00000111271 Protein coding intron GSE100210 HepG2 cell line chr12:111688138..111688139 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BOCA 1 - Human_RBP_ID_24930631 Human_Splice_Rec_1425618,Human_Splice_Rec_1425619 RMVar_hsa_circ_87833,RMVar_hsa_circ_160020 54616 RMVar_ID_54616 Human_SNP_ID_815560738 A-to-I Human chr12 - 98455516 98455516 98455516 TGTTGTCATGGCTTAATATCAGAGTTAGCATCAAGGAGCCCTCCAAAGAGGACCACAACGAACAC TGTTGTCATGGCTTAATATCAGAGTTAGCATCGAGGAGCCCTCCAAAGAGGACCACAACGAACAC T C SLC9A7P1 Ensembl:ENSG00000227825 Pseudogene exon GSE100210 HepG2 cell line chr12:98455515..98455516 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC 33..33 33 LIHC 2 - 54617 RMVar_ID_54617 Human_SNP_ID_815581019 A-to-I Human chr12 + 19443513 19443513 19443513 GGCCGAGTCGGGTGGATCATTTGAGGTCAAGGAATTCCAAGACCAGCCTGGACAACATGGTGAAA GGCCGAGTCGGGTGGATCATTTGAGGTCAAGGGATTCCAAGACCAGCCTGGACAACATGGTGAAA A G AEBP2 Ensembl:ENSG00000139154 Protein coding intron GSE38233 cultured B-cells chr12:19443513..19443514 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma,breast HER-positive_carcinoma 9 breast RMVar_hsa_circ_126552,RMVar_hsa_circ_155163 54618 RMVar_ID_54618 Human_SNP_ID_815620919 A-to-I Human chr12 + 56511523 56511523 56511523 ACCACCCCTGAAGAAATTGCACAGGTTGCTACAATTTCTGCAAACGGAGACAAAGAAATTGGCAA ACCACCCCTGAAGAAATTGCACAGGTTGCTACGATTTCTGCAAACGGAGACAAAGAAATTGGCAA A G HSPD1P4 Ensembl:ENSG00000257576 Pseudogene exon GSE100210 HepG2 cell line chr12:56511522..56511523 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_17358678 54619 RMVar_ID_54619 Human_SNP_ID_815626251 A-to-I Human chr12 + 6727686 6727686 6727686 TTCAACTCTGAATTTAGGGTAGGAATTGGATGACGTATGGAGCAAGAGGGCATTGTGGTTTGGGA TTCAACTCTGAATTTAGGGTAGGAATTGGATGGCGTATGGAGCAAGAGGGCATTGTGGTTTGGGA A G COPS7A Ensembl:ENSG00000111652 Protein coding intron GSE38233 cultured B-cells chr12:6727685..6727686 24183664 RNA-Seq:(High) rs7138427 Functional Loss SNV ICGC 33..33 33 COCA 5 - Human_Splice_Rec_1331896 GWAS_ID_3862 RMVar_hsa_circ_12814,RMVar_hsa_circ_36664,RMVar_hsa_circ_289996 54620 RMVar_ID_54620 Human_SNP_ID_815638055 A-to-I Human chr12 + 110342439 110342439 110342439 CATCCGCTACCTCATCTCGTCCAACGTCGGGGAAGTTGTCTGGTAGGTCTCTGTGACAGCATCAC CATCCGCTACCTCATCTCGTCCAACGTCGGGGGAGTTGTCTGGTAGGTCTCTGTGACAGCATCAC A G ATP2A2 Ensembl:ENSG00000174437 Protein coding CDS GSE100210 HepG2 cell line chr12:110342438..110342439 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_410173,Human_RBP_ID_811680,Human_RBP_ID_8775787,Human_RBP_ID_9365553,Human_RBP_ID_18617214,Human_RBP_ID_19056794,Human_RBP_ID_22437410,Human_RBP_ID_22756489 Human_Splice_Rec_1422967,Human_Splice_Rec_1423005,Human_Splice_Rec_1423037,Human_Splice_Rec_1423067 RMVar_hsa_circ_159820,RMVar_hsa_circ_101430,RMVar_hsa_circ_16970,RMVar_hsa_circ_267949,RMVar_hsa_circ_159821,RMVar_hsa_circ_57837,RMVar_hsa_circ_70026,RMVar_hsa_circ_277340,RMVar_hsa_circ_83406,RMVar_hsa_circ_159826,RMVar_hsa_circ_159827,RMVar_hsa_circ_88883,RMVar_hsa_circ_159830,RMVar_hsa_circ_112332,RMVar_hsa_circ_159832,RMVar_hsa_circ_331767,RMVar_hsa_circ_159831,RMVar_hsa_circ_278068,RMVar_hsa_circ_159833,RMVar_hsa_circ_296343 54621 RMVar_ID_54621 Human_SNP_ID_815654415 A-to-I Human chr12 + 68143503 68143503 68143503 AAGGTCCTGCTGGTTGGGGCAGACAACTTCACACTGCTTGGCAAGCCACTCCTCAGAAAGGATCT AAGGTCCTGCTGGTTGGGGCAGACAACTTCACGCTGCTTGGCAAGCCACTCCTCAGAAAGGATCT A G AC007458.1,IFNG-AS1 Ensembl:ENSG00000256708,Ensembl:ENSG00000255733 Pseudogene,lincRNA exon,intron GSE100210 HepG2 cell line chr12:68143502..68143503 29129909 RNA-Seq:(High) rs11555388 Functional Loss SNV ICGC 33..33 33 LAML 1 - 54622 RMVar_ID_54622 Human_SNP_ID_815694273 A-to-I Human chr12 - 92531186 92531186 92531186 AATCTATCCATGCAGTATACATTGGGGAGTAAAGAGGGCATCCACCAGCAAAACCACAGTTGTTG AATCTATCCATGCAGTATACATTGGGGAGTAAGGAGGGCATCCACCAGCAAAACCACAGTTGTTG T C - - Other Unknown GSE100210 HepG2 cell line chr12:92531185..92531186 29129909 RNA-Seq:(High) rs1040304737 Functional Loss SNV ICGC 33..33 33 COCA 1 - 54623 RMVar_ID_54623 Human_SNP_ID_815702303 A-to-I Human chr12 - 110399403 110399403 110399403 AGACTCTAGGCTCAAGCAGTCTTCCCACCTCAACCTCCCAAAGTGTTGGGATTACAGGTGTGAGC AGACTCTAGGCTCAAGCAGTCTTCCCACCTCAGCCTCCCAAAGTGTTGGGATTACAGGTGTGAGC T C AC144548.1,ANAPC7 Ensembl:ENSG00000258210,Ensembl:ENSG00000196510 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line chr12:110399402..110399403 29129909 RNA-Seq:(High) rs1357729699 Functional Loss SNV ICGC 33..33 33 PRAD 1 - Human_RBP_ID_5246482,Human_RBP_ID_11806150,Human_RBP_ID_17561266 RMVar_hsa_circ_98968,RMVar_hsa_circ_159857 54624 RMVar_ID_54624 Human_SNP_ID_815791206 A-to-I Human chr12 - 10172078 10172078 10172078 CTTCACTCTCTCATTCTTAGCTTGAATTTGGAAATGACTTTTGATGACCTAAAGATCCAGACTGT CTTCACTCTCTCATTCTTAGCTTGAATTTGGACATGACTTTTGATGACCTAAAGATCCAGACTGT T G OLR1 Ensembl:ENSG00000173391 Protein coding 5'UTR GSE100210 HepG2 cell line chr12:10172077..10172078 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 5 large intestine Human_RBP_ID_37045,Human_RBP_ID_2298949 Human_Splice_Rec_1338521,Human_Splice_Rec_1338531,Human_Splice_Rec_1338543,Human_Splice_Rec_1338551 54625 RMVar_ID_54625 Human_SNP_ID_815830661 A-to-I Human chr12 - 79690106 79690106 79690106 CCCCGGGCCCGGCCCCCCCGGGAGGGGGCAGCAGCGACGCCGCTGGGAAGCCCCCCGCGGGGGCT CCCCGGGCCCGGCCCCCCCGGGAGGGGGCAGCGGCGACGCCGCTGGGAAGCCCCCCGCGGGGGCT T C PAWR Ensembl:ENSG00000177425 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector chr12:79690105..79690106 29967493 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 1 lung Human_RBP_ID_230154,Human_RBP_ID_873191,Human_RBP_ID_9366700 RMVar_hsa_circ_63770 54626 RMVar_ID_54626 Human_SNP_ID_815939451 A-to-I Human chr12 + 120569029 120569029 120569029 TTTCGCTCTTGTTGCCCAGGCTGGAGTGCAATAGTGCAATCTCAGCTTACTGCAACCTCTGCCTC TTTCGCTCTTGTTGCCCAGGCTGGAGTGCAATGGTGCAATCTCAGCTTACTGCAACCTCTGCCTC A G RNF10 Ensembl:ENSG00000022840 Protein coding intron GSE38233 cultured B-cells chr12:120569028..120569029 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_88407,RMVar_hsa_circ_86391,RMVar_hsa_circ_160802,RMVar_hsa_circ_160803,RMVar_hsa_circ_307791,RMVar_hsa_circ_27491,RMVar_hsa_circ_160816,RMVar_hsa_circ_327844,RMVar_hsa_circ_160810,RMVar_hsa_circ_375920,RMVar_hsa_circ_160815,RMVar_hsa_circ_37149,RMVar_hsa_circ_83786,RMVar_hsa_circ_160817,RMVar_hsa_circ_84745,RMVar_hsa_circ_88087,RMVar_hsa_circ_16332,RMVar_hsa_circ_160825,RMVar_hsa_circ_160828,RMVar_hsa_circ_309102,RMVar_hsa_circ_160826,RMVar_hsa_circ_376353,RMVar_hsa_circ_160829,RMVar_hsa_circ_122660,RMVar_hsa_circ_286489,RMVar_hsa_circ_106013,RMVar_hsa_circ_160830,RMVar_hsa_circ_160831,RMVar_hsa_circ_160832 54627 RMVar_ID_54627 Human_SNP_ID_815956578 A-to-I Human chr12 + 101066804 101066804 101066804 GGACCACAGGAAGCTGAGATCTGTATCTGTGGACCTGAATGTTGATCCCTCACTTCAGATTGACA GGACCACAGGAAGCTGAGATCTGTATCTGTGGGCCTGAATGTTGATCCCTCACTTCAGATTGACA A G ANO4,AC063947.2 Ensembl:ENSG00000151572,Ensembl:ENSG00000258033 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line chr12:101066803..101066804 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_1082447,Human_RBP_ID_23531658 RMVar_hsa_circ_1222,RMVar_hsa_circ_37792,RMVar_hsa_circ_29557,RMVar_hsa_circ_319067,RMVar_hsa_circ_325021,RMVar_hsa_circ_15684,RMVar_hsa_circ_159211,RMVar_hsa_circ_314921,RMVar_hsa_circ_43130,RMVar_hsa_circ_159210,RMVar_hsa_circ_267263,RMVar_hsa_circ_159215,RMVar_hsa_circ_20881,RMVar_hsa_circ_159217,RMVar_hsa_circ_15080,RMVar_hsa_circ_45345,RMVar_hsa_circ_315340,RMVar_hsa_circ_277080,RMVar_hsa_circ_17868,RMVar_hsa_circ_159219,RMVar_hsa_circ_159220,RMVar_hsa_circ_159218,RMVar_hsa_circ_159216 54628 RMVar_ID_54628 Human_SNP_ID_815961749 A-to-I Human chr12 + 125588380 125588380 125588380 AATCCCCAGTCTCACTGGGTCATCCAGGCTGGAGTGCAGTGGCGTGATCTCGGCTTACTGCAGCC AATCCCCAGTCTCACTGGGTCATCCAGGCTGGTGTGCAGTGGCGTGATCTCGGCTTACTGCAGCC A T TMEM132B Ensembl:ENSG00000139364 Protein coding intron GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank;ASD brains,temporal_cortex chr12:125588379..125588380 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 RECA 1 - 54629 RMVar_ID_54629 Human_SNP_ID_815971103 A-to-I Human chr12 + 1398101 1398101 1398101 AACCTCCCAGGCTCAATCGATCCTCCCACCTCAGCCTCCCAAGTAGCTGGGACTGCGGGCACATG AACCTCCCAGGCTCAATCGATCCTCCCACCTCCGCCTCCCAAGTAGCTGGGACTGCGGGCACATG A C ERC1 Ensembl:ENSG00000082805 Protein coding intron GSE100210 HepG2 cell line chr12:1398100..1398101 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BOCA 1 - RMVar_hsa_circ_20106,RMVar_hsa_circ_92073,RMVar_hsa_circ_154233,RMVar_hsa_circ_363760,RMVar_hsa_circ_341490,RMVar_hsa_circ_69245,RMVar_hsa_circ_39259,RMVar_hsa_circ_315604,RMVar_hsa_circ_326696,RMVar_hsa_circ_154258,RMVar_hsa_circ_276587,RMVar_hsa_circ_293183,RMVar_hsa_circ_312382,RMVar_hsa_circ_154259,RMVar_hsa_circ_154267,RMVar_hsa_circ_290815,RMVar_hsa_circ_318201,RMVar_hsa_circ_283022,RMVar_hsa_circ_154265,RMVar_hsa_circ_154266 54630 RMVar_ID_54630 Human_SNP_ID_816070397 A-to-I Human chr12 + 125027947 125027947 125027947 CTGACCTCGTGATCCGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGCG CTGACCTCGTGATCCGCCCGCCTCGGCCTCCCGAAGTGCTGGGATTACAGGCGTGAGCCACCGCG A G BRI3BP Ensembl:ENSG00000184992 Protein coding 3'UTR GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line chr12:125027947..125027948 31158229 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 54631 RMVar_ID_54631 Human_SNP_ID_816091035 A-to-I Human chr12 + 93394072 93394072 93394072 TCACCCATGCTGGAGTATGGTGGCACGATCTCAGTTCATTGCAACCTCCACCTCCTGGGTTCAAG TCACCCATGCTGGAGTATGGTGGCACGATCTCGGTTCATTGCAACCTCCACCTCCTGGGTTCAAG A G NUDT4 Ensembl:ENSG00000173598 Protein coding intron GSE38233 cultured B-cells chr12:93394071..93394072 24183664 RNA-Seq:(High) rs2035052 Functional Loss SNV COSMIC 33..33 33 oesophagus adenocarcinoma 5 oesophagus 54632 RMVar_ID_54632 Human_SNP_ID_816103152 A-to-I Human chr12 + 43950679 43950679 43950679 CCTGGTGATCAGCAGCTTCCCGATAAGCTCTCAGAAGTTGGGCTAGTGGGCTCAAGCATGTGCAC CCTGGTGATCAGCAGCTTCCCGATAAGCTCTCTGAAGTTGGGCTAGTGGGCTCAAGCATGTGCAC A T TMEM117 Ensembl:ENSG00000139173 Protein coding intron GSE100210 HepG2 cell line chr12:43950678..43950679 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_50125 54633 RMVar_ID_54633 Human_SNP_ID_816121920 A-to-I Human chr12 + 12851099 12851099 12851099 AGAAGCTTATGGCCACAGAAGTTGCTGCTGACACTCTGGGTGAAGAATGGAAAGGTTATGTGGTC AGAAGCTTATGGCCACAGAAGTTGCTGCTGACGCTCTGGGTGAAGAATGGAAAGGTTATGTGGTC A G AC007688.2 Ensembl:ENSG00000241352 Pseudogene exon GSE100210 HepG2 cell line chr12:12851098..12851099 29129909 RNA-Seq:(High) rs878890930 Functional Loss SNV ICGC 33..33 33 LAML 2 - 54634 RMVar_ID_54634 Human_SNP_ID_816135364 A-to-I Human chr12 + 64449052 64449052 64449052 GAAACCCCATCTCTACTAAAAATACAACAGCCAGGTGTGATGGTGCACGCTCGTAATCCCGGCTA GAAACCCCATCTCTACTAAAAATACAACAGCCGGGTGTGATGGTGCACGCTCGTAATCCCGGCTA A G XPOT Ensembl:ENSG00000184575 Protein coding 3'UTR GSE38233 cultured B-cells chr12:64449051..64449052 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_425523,Human_RBP_ID_6207468,Human_RBP_ID_8381497,Human_RBP_ID_17824494,Human_RBP_ID_26418866 54635 RMVar_ID_54635 Human_SNP_ID_816142648 A-to-I Human chr12 - 26914081 26914078 26914081 AGTGTTATTGTGAAAGAATCTCTGACAGAAGAAGATGTGTTAAACTGTCAAAAAACAATATACAA AGTGTTATTGTGAAAGAATCTCTGACAGAAGA___TGTGTTAAACTGTCAAAAAACAATATACAA ATCT A INTS13 Ensembl:ENSG00000064102 Protein coding CDS GSE100210 HepG2 cell line chr12:26914080..26914081 29129909 RNA-Seq:(High) rs1334876338 Functional Loss DEL TCGA 33..35 33 UCEC 1 - Human_RBP_ID_1469991,Human_RBP_ID_1793044 Human_Splice_Rec_1349118,Human_Splice_Rec_1349150,Human_Splice_Rec_1349170,Human_Splice_Rec_1349178 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 54636 RMVar_ID_54636 Human_SNP_ID_816155762 A-to-I Human chr12 - 55980701 55980701 55980701 AACTGGATGAAAAGCATCATGGAGAATGCCTCAGCTGGGGTGGAGCACCTCTTGCTAGGGAACAA AACTGGATGAAAAGCATCATGGAGAATGCCTCGGCTGGGGTGGAGCACCTCTTGCTAGGGAACAA T C AC034102.1 Ensembl:ENSG00000237493 Pseudogene exon GSE100210 HepG2 cell line chr12:55980700..55980701 29129909 RNA-Seq:(High) rs878918968 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue 54637 RMVar_ID_54637 Human_SNP_ID_816179668 A-to-I Human chr12 - 112206395 112206395 112206395 AAACTCTTGGGCTCAAGAGATCCTCCTGCTTCAGCTTCCCGAGTACCTGGGACTACAGGCACTCA AAACTCTTGGGCTCAAGAGATCCTCCTGCTTCGGCTTCCCGAGTACCTGGGACTACAGGCACTCA T C HECTD4 Ensembl:ENSG00000173064 Protein coding intron GSE38233 cultured B-cells chr12:112206394..112206395 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - RMVar_hsa_circ_76071,RMVar_hsa_circ_266793,RMVar_hsa_circ_269340,RMVar_hsa_circ_92283,RMVar_hsa_circ_265564,RMVar_hsa_circ_86521,RMVar_hsa_circ_96738,RMVar_hsa_circ_160134,RMVar_hsa_circ_160135,RMVar_hsa_circ_160133,RMVar_hsa_circ_86374,RMVar_hsa_circ_160136,RMVar_hsa_circ_160137,RMVar_hsa_circ_266836,RMVar_hsa_circ_16871,RMVar_hsa_circ_160139,RMVar_hsa_circ_120037,RMVar_hsa_circ_56551,RMVar_hsa_circ_17528,RMVar_hsa_circ_78078,RMVar_hsa_circ_90046,RMVar_hsa_circ_110981,RMVar_hsa_circ_269059,RMVar_hsa_circ_269436,RMVar_hsa_circ_120958,RMVar_hsa_circ_99564,RMVar_hsa_circ_104560,RMVar_hsa_circ_99507,RMVar_hsa_circ_82647,RMVar_hsa_circ_88433,RMVar_hsa_circ_79943,RMVar_hsa_circ_98741,RMVar_hsa_circ_160146,RMVar_hsa_circ_160148,RMVar_hsa_circ_160150,RMVar_hsa_circ_160152,RMVar_hsa_circ_160151,RMVar_hsa_circ_160149,RMVar_hsa_circ_160147,RMVar_hsa_circ_160144,RMVar_hsa_circ_160145,RMVar_hsa_circ_160143,RMVar_hsa_circ_92094,RMVar_hsa_circ_160155,RMVar_hsa_circ_81719,RMVar_hsa_circ_160154,RMVar_hsa_circ_160156,RMVar_hsa_circ_5824,RMVar_hsa_circ_22381,RMVar_hsa_circ_358670,RMVar_hsa_circ_84481,RMVar_hsa_circ_160158,RMVar_hsa_circ_23033,RMVar_hsa_circ_347738,RMVar_hsa_circ_32340,RMVar_hsa_circ_12086,RMVar_hsa_circ_160161,RMVar_hsa_circ_91992,RMVar_hsa_circ_331663,RMVar_hsa_circ_340174,RMVar_hsa_circ_326154,RMVar_hsa_circ_272179,RMVar_hsa_circ_160163,RMVar_hsa_circ_160164,RMVar_hsa_circ_160162,RMVar_hsa_circ_160167,RMVar_hsa_circ_84639,RMVar_hsa_circ_309283,RMVar_hsa_circ_330623,RMVar_hsa_circ_372646,RMVar_hsa_circ_119357,RMVar_hsa_circ_160169,RMVar_hsa_circ_52073,RMVar_hsa_circ_160170,RMVar_hsa_circ_160168,RMVar_hsa_circ_160166 54638 RMVar_ID_54638 Human_SNP_ID_816192480 A-to-I Human chr12 - 3840767 3840767 3840767 TTGCATATTTATCATCAGTAATATTCTCCAATATGCTTGGTTCGGGTCTTTTATCCAACTATGTC TTGCATATTTATCATCAGTAATATTCTCCAATGTGCTTGGTTCGGGTCTTTTATCCAACTATGTC T C PARP11 Ensembl:ENSG00000111224 Protein coding intron GSE100210 HepG2 cell line chr12:3840766..3840767 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 8 haematopoietic and lymphoid tissue RMVar_hsa_circ_154373,RMVar_hsa_circ_154375,RMVar_hsa_circ_154377,RMVar_hsa_circ_285659,RMVar_hsa_circ_154379,RMVar_hsa_circ_307799,RMVar_hsa_circ_154380 54639 RMVar_ID_54639 Human_SNP_ID_816285071 A-to-I Human chr12 + 105151653 105151653 105151653 AAAGGTGCACACCACCACACCCAGCTAATTTTAGTATTTTTAGTAGAGATGGGGTTTCACCATAT AAAGGTGCACACCACCACACCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATAT A T WASHC4 Ensembl:ENSG00000136051 Protein coding intron GSE38233 cultured B-cells chr12:105151652..105151653 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_37136,RMVar_hsa_circ_354817,RMVar_hsa_circ_42554,RMVar_hsa_circ_2601,RMVar_hsa_circ_6079,RMVar_hsa_circ_34317,RMVar_hsa_circ_344616,RMVar_hsa_circ_339409,RMVar_hsa_circ_159464,RMVar_hsa_circ_341948,RMVar_hsa_circ_108083,RMVar_hsa_circ_70568,RMVar_hsa_circ_352641,RMVar_hsa_circ_159468,RMVar_hsa_circ_57806,RMVar_hsa_circ_16195,RMVar_hsa_circ_74170,RMVar_hsa_circ_14939,RMVar_hsa_circ_54873,RMVar_hsa_circ_7055,RMVar_hsa_circ_300722,RMVar_hsa_circ_367358,RMVar_hsa_circ_299786,RMVar_hsa_circ_159474,RMVar_hsa_circ_159475 54640 RMVar_ID_54640 Human_SNP_ID_816426169 A-to-I Human chr12 - 48655474 48655462 48655475 GCCTCTGCGTCCCAAGCTTGAGGGATCCTCCCACCTCAACCTCCAGAGTAGCTGGGACTACAGGT GCCTCTGCGTCCCAAGCTTGAGGGATCCTCC_____________AGAGTAGCTGGGACTACAGGT TGGAGGTTGAGGTG T KANSL2 Ensembl:ENSG00000139620 Protein coding intron GSE100210 HepG2 cell line chr12:48655473..48655474 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 32..44 33 RECA 1 - Human_RBP_ID_11950968 RMVar_hsa_circ_79268,RMVar_hsa_circ_156186 54641 RMVar_ID_54641 Human_SNP_ID_816440479 A-to-I Human chr12 + 27030182 27030182 27030182 TTTTTAAGGTGAAGTCTCTGTCACCCAAGCTGAAGTGCAGTTCTGTGATCATGGCTCACTGCAGC TTTTTAAGGTGAAGTCTCTGTCACCCAAGCTGGAGTGCAGTTCTGTGATCATGGCTCACTGCAGC A G MED21 Ensembl:ENSG00000152944 Protein coding CDS GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE123020:GSM3490832,GSM3490833,GSM3490834;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BEP2D cell line;esophageal squamous carcinoma cells,KYSE180 cell line;esophageal squamous carcinoma cells,KYSE180 cell line chr12:27030181..27030182;chr12:27030182..27030183 24183664,31158229,31158229,32596459,32596459 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue Human_RBP_ID_6169683,Human_RBP_ID_11913442,Human_RBP_ID_17684160 Human_Splice_Rec_1349400 54642 RMVar_ID_54642 Human_SNP_ID_816464849 A-to-I Human chr12 + 1159136 1159136 1159136 ACTATAATGAATGAATTGATTTCCTCTCAGGTAGCATGTATCAGTTTTGGACAGTTTTGACCCTA ACTATAATGAATGAATTGATTTCCTCTCAGGTGGCATGTATCAGTTTTGGACAGTTTTGACCCTA A G ERC1 Ensembl:ENSG00000082805 Protein coding intron GSE107867 ASD brains,cerebellum chr12:1159135..1159136 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_92073,RMVar_hsa_circ_154233,RMVar_hsa_circ_360114,RMVar_hsa_circ_366027,RMVar_hsa_circ_363760,RMVar_hsa_circ_341490,RMVar_hsa_circ_310476,RMVar_hsa_circ_21731,RMVar_hsa_circ_53620,RMVar_hsa_circ_359278,RMVar_hsa_circ_367777,RMVar_hsa_circ_355693,RMVar_hsa_circ_13451,RMVar_hsa_circ_373716,RMVar_hsa_circ_154241,RMVar_hsa_circ_154244,RMVar_hsa_circ_352302,RMVar_hsa_circ_53789,RMVar_hsa_circ_42167,RMVar_hsa_circ_303710,RMVar_hsa_circ_26497,RMVar_hsa_circ_154245,RMVar_hsa_circ_62468,RMVar_hsa_circ_329155 54643 RMVar_ID_54643 Human_SNP_ID_816470113 A-to-I Human chr12 - 53178222 53178222 53178222 GCTATCCATTGGCCTCGGCCTCCTAGAGTGCTAGGATTACAGGATTGAGCCACCATGCCTGGCCG GCTATCCATTGGCCTCGGCCTCCTAGAGTGCTGGGATTACAGGATTGAGCCACCATGCCTGGCCG T C CSAD Ensembl:ENSG00000139631 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line chr12:53178221..53178222 24183664,29129909,31158229,31158229,31158229 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 5 haematopoietic and lymphoid tissue Human_RBP_ID_11973451 54644 RMVar_ID_54644 Human_SNP_ID_816497424 A-to-I Human chr12 + 95224384 95224384 95224384 TGCCTAGGCTGGAATGCAGTGTTAACCATCATAACTCACTGCAGCCTCCAACTCCTGGCTCAGGT TGCCTAGGCTGGAATGCAGTGTTAACCATCATGACTCACTGCAGCCTCCAACTCCTGGCTCAGGT A G VEZT Ensembl:ENSG00000028203 Protein coding intron GSE100210 HepG2 cell line chr12:95224383..95224384 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue 54645 RMVar_ID_54645 Human_SNP_ID_816519771 A-to-I Human chr12 - 123208873 123208873 123208873 TAAAAAATTCTGGCTGGCTTGAGCTGGGCATCATAGTTTACACCTGTAATCCTTGTACTTTGGGA TAAAAAATTCTGGCTGGCTTGAGCTGGGCATCGTAGTTTACACCTGTAATCCTTGTACTTTGGGA T C MPHOSPH9 Ensembl:ENSG00000051825 Protein coding intron GSE38233 cultured B-cells chr12:123208872..123208873 24183664 RNA-Seq:(High) rs11057192 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_11863102,Human_RBP_ID_17561568 GWAS_ID_4034,GWAS_ID_4035,GWAS_ID_4036,GWAS_ID_4037,GWAS_ID_4038,GWAS_ID_4039,GWAS_ID_4040,GWAS_ID_4041 RMVar_hsa_circ_428,RMVar_hsa_circ_98333,RMVar_hsa_circ_161238,RMVar_hsa_circ_344902,RMVar_hsa_circ_274631,RMVar_hsa_circ_161240,RMVar_hsa_circ_161239,RMVar_hsa_circ_112150,RMVar_hsa_circ_115396,RMVar_hsa_circ_161248,RMVar_hsa_circ_161249,RMVar_hsa_circ_305866,RMVar_hsa_circ_76789,RMVar_hsa_circ_161251,RMVar_hsa_circ_161254,RMVar_hsa_circ_109269,RMVar_hsa_circ_283259,RMVar_hsa_circ_161255,RMVar_hsa_circ_294399,RMVar_hsa_circ_33850,RMVar_hsa_circ_123741,RMVar_hsa_circ_335986,RMVar_hsa_circ_25389,RMVar_hsa_circ_161271,RMVar_hsa_circ_50666,RMVar_hsa_circ_161267,RMVar_hsa_circ_115836,RMVar_hsa_circ_350629,RMVar_hsa_circ_161269,RMVar_hsa_circ_366477,RMVar_hsa_circ_306725,RMVar_hsa_circ_45145,RMVar_hsa_circ_291940,RMVar_hsa_circ_296586,RMVar_hsa_circ_161273,RMVar_hsa_circ_161272,RMVar_hsa_circ_26213,RMVar_hsa_circ_371106,RMVar_hsa_circ_161270,RMVar_hsa_circ_34604,RMVar_hsa_circ_161279,RMVar_hsa_circ_83435,RMVar_hsa_circ_374801,RMVar_hsa_circ_161277,RMVar_hsa_circ_354704,RMVar_hsa_circ_161278,RMVar_hsa_circ_161280 54646 RMVar_ID_54646 Human_SNP_ID_816525182 A-to-I Human chr12 + 49510425 49510425 49510425 TCTCTACAAAAAATGTAAAAAATTAGCTGGGCATGGTAGCTCGTGCCTGTAGTCCCAGCTACTTA TCTCTACAAAAAATGTAAAAAATTAGCTGGGCGTGGTAGCTCGTGCCTGTAGTCCCAGCTACTTA A G SPATS2 Ensembl:ENSG00000123352 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr12:49510424..49510425 24183664,29129909 RNA-Seq:(High) rs916675172 Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_33086,RMVar_hsa_circ_349686,RMVar_hsa_circ_44098,RMVar_hsa_circ_156340,RMVar_hsa_circ_156341,RMVar_hsa_circ_31328,RMVar_hsa_circ_306561,RMVar_hsa_circ_156343 54647 RMVar_ID_54647 Human_SNP_ID_816546765 A-to-I Human chr12 + 49272831 49272831 49272831 CGCCATGGTAAATACATGGCTTGCTGCCTGTTATACCGTGGTGACGTGGTTCCCAAAGATGTCAA CGCCATGGTAAATACATGGCTTGCTGCCTGTTGTACCGTGGTGACGTGGTTCCCAAAGATGTCAA A G TUBA1C Ensembl:ENSG00000167553 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr12:49272830..49272831 30559470 RNA-Seq:(High) rs538625739 Functional Loss SNV ICGC 33..33 33 NKTL 1 - Human_RBP_ID_420863,Human_RBP_ID_992579,Human_RBP_ID_1166986,Human_RBP_ID_1357667,Human_RBP_ID_1472650,Human_RBP_ID_1796057,Human_RBP_ID_2339963,Human_RBP_ID_4225275,Human_RBP_ID_6190726,Human_RBP_ID_8377171,Human_RBP_ID_8782349,Human_RBP_ID_9017686,Human_RBP_ID_9255238,Human_RBP_ID_9278088,Human_RBP_ID_17650641,Human_RBP_ID_17668954,Human_RBP_ID_22037822,Human_RBP_ID_22174390,Human_RBP_ID_22435842,Human_RBP_ID_22755892,Human_RBP_ID_23125600,Human_RBP_ID_23561892,Human_RBP_ID_26768247,Human_RBP_ID_26907130,Human_RBP_ID_27214942,Human_RBP_ID_27629915 Human_miRNA_ID_497410,Human_miRNA_ID_2171892 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 54648 RMVar_ID_54648 Human_SNP_ID_816547280 A-to-I Human chr12 + 16400229 16400229 16400229 CACTTCTGTGTAGAACTGCACATCCATGTGCCACTTCTTCCCAAACATGATGGCATTCTTGAGGT CACTTCTGTGTAGAACTGCACATCCATGTGCCGCTTCTTCCCAAACATGATGGCATTCTTGAGGT A G MGST1 Ensembl:ENSG00000008394 Protein coding intron GSE100210 HepG2 cell line chr12:16400228..16400229 29129909 RNA-Seq:(High) rs1287855694 Functional Loss SNV ICGC 33..33 33 LAML 1 - 54649 RMVar_ID_54649 Human_SNP_ID_816556171 A-to-I Human chr12 - 66149253 66149253 66149253 TGTTTTTCGTAGAGAGGGGGTTTTGCTGTGTCACCCAGGCTGGTCTCAAACTCCTGGACTCAAGC TGTTTTTCGTAGAGAGGGGGTTTTGCTGTGTCCCCCAGGCTGGTCTCAAACTCCTGGACTCAAGC T G TMBIM4,AC078927.1 Ensembl:ENSG00000155957,Ensembl:ENSG00000228144 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line chr12:66149252..66149253 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 OV 1 - RMVar_hsa_circ_5887,RMVar_hsa_circ_157982,RMVar_hsa_circ_66181,RMVar_hsa_circ_30947,RMVar_hsa_circ_90614,RMVar_hsa_circ_271599,RMVar_hsa_circ_157983,RMVar_hsa_circ_157984,RMVar_hsa_circ_157985 54650 RMVar_ID_54650 Human_SNP_ID_816558809 A-to-I Human chr12 + 51050254 51050254 51050254 TTTATTATGAATTTTTTTTTTTTTTGAGTCTCACCGTGTCGCCCAGGCTGGAGTGCAATGGCATG TTTATTATGAATTTTTTTTTTTTTTGAGTCTCTCCGTGTCGCCCAGGCTGGAGTGCAATGGCATG A T LETMD1 Ensembl:ENSG00000050426 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr12:51050253..51050254 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_2342317,Human_RBP_ID_11968343 RMVar_hsa_circ_3549,RMVar_hsa_circ_332234,RMVar_hsa_circ_24451,RMVar_hsa_circ_276574,RMVar_hsa_circ_280689,RMVar_hsa_circ_99391,RMVar_hsa_circ_156557,RMVar_hsa_circ_156558,RMVar_hsa_circ_156556 54651 RMVar_ID_54651 Human_SNP_ID_816580957 A-to-I Human chr12 + 116845121 116845121 116845121 AAAAAATTAGCCAGGCATGGTGGCACGTGCCTATAGTTGTAGCTACTTGGGAGATTGAAGCAGGA AAAAAATTAGCCAGGCATGGTGGCACGTGCCTGTAGTTGTAGCTACTTGGGAGATTGAAGCAGGA A G RNFT2 Ensembl:ENSG00000135119 Protein coding intron GSE100210 HepG2 cell line chr12:116845120..116845121 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 1 - 54652 RMVar_ID_54652 Human_SNP_ID_816599695 A-to-I Human chr12 + 113283470 113283470 113283470 CAGCCTGGGCAATGTGGCAAAACCCCATCTCTACAAAAAATACAAAAATTAGCTGGCGTGGTGGT CAGCCTGGGCAATGTGGCAAAACCCCATCTCTGCAAAAAATACAAAAATTAGCTGGCGTGGTGGT A G TPCN1 Ensembl:ENSG00000186815 Protein coding intron GSE38233 cultured B-cells chr12:113283469..113283470 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_86814,RMVar_hsa_circ_84130,RMVar_hsa_circ_116531,RMVar_hsa_circ_91686,RMVar_hsa_circ_160330,RMVar_hsa_circ_160331,RMVar_hsa_circ_160332,RMVar_hsa_circ_111472,RMVar_hsa_circ_30367,RMVar_hsa_circ_160334,RMVar_hsa_circ_160337,RMVar_hsa_circ_160333,RMVar_hsa_circ_335839,RMVar_hsa_circ_86234,RMVar_hsa_circ_160341,RMVar_hsa_circ_106688,RMVar_hsa_circ_160344,RMVar_hsa_circ_91768,RMVar_hsa_circ_160347,RMVar_hsa_circ_160346,RMVar_hsa_circ_375162,RMVar_hsa_circ_160348,RMVar_hsa_circ_123699 54653 RMVar_ID_54653 Human_SNP_ID_816634528 A-to-I Human chr12 - 123159142 123159142 123159142 AATAATAAAAAAAAATACCTGCCAATGTGATCATTTTTTAAAAGGTGTGGGGTTGTCTTGGCTAA AATAATAAAAAAAAATACCTGCCAATGTGATCGTTTTTTAAAAGGTGTGGGGTTGTCTTGGCTAA T C MPHOSPH9 Ensembl:ENSG00000051825 Protein coding intron GSE38233 cultured B-cells chr12:123159141..123159142 24183664 RNA-Seq:(High) rs2851438 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_2310521,Human_RBP_ID_3396860 GWAS_ID_3946 RMVar_hsa_circ_81544,RMVar_hsa_circ_98333,RMVar_hsa_circ_161237,RMVar_hsa_circ_161238 54654 RMVar_ID_54654 Human_SNP_ID_816650170 A-to-I Human chr12 - 46359638 46359638 46359638 CGTCACAGTGTATGGTGAATATATTATTAAATAATGTGGTACTTCGCTCATCAGGCATAATGTCT CGTCACAGTGTATGGTGAATATATTATTAAATGATGTGGTACTTCGCTCATCAGGCATAATGTCT T C SLC38A2 Ensembl:ENSG00000134294 Protein coding 3'UTR GSE100210 HepG2 cell line chr12:46359637..46359638 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC 33..33 33 UCEC 2 - Human_RBP_ID_419919,Human_RBP_ID_992251,Human_RBP_ID_1166802,Human_RBP_ID_1269225,Human_RBP_ID_1471777,Human_RBP_ID_1795314,Human_RBP_ID_2338312,Human_RBP_ID_3406083,Human_RBP_ID_4222587,Human_RBP_ID_6186906,Human_RBP_ID_8376098,Human_RBP_ID_8781508,Human_RBP_ID_9017368,Human_RBP_ID_11945750,Human_RBP_ID_17238406,Human_RBP_ID_17354270,Human_RBP_ID_17471269,Human_RBP_ID_17685747,Human_RBP_ID_17819484,Human_RBP_ID_18260508,Human_RBP_ID_22383220,Human_RBP_ID_22904100,Human_RBP_ID_23560196,Human_RBP_ID_24466256,Human_RBP_ID_24971703,Human_RBP_ID_26416004,Human_RBP_ID_27629384 Human_miRNA_ID_126837,Human_miRNA_ID_920321,Human_miRNA_ID_2943579 RMVar_hsa_circ_113045,RMVar_hsa_circ_124081,RMVar_hsa_circ_125589,RMVar_hsa_circ_114088,RMVar_hsa_circ_90493,RMVar_hsa_circ_96200,RMVar_hsa_circ_112311,RMVar_hsa_circ_95051,RMVar_hsa_circ_156113,RMVar_hsa_circ_156117,RMVar_hsa_circ_156119,RMVar_hsa_circ_89986,RMVar_hsa_circ_156120,RMVar_hsa_circ_156118,RMVar_hsa_circ_156115,RMVar_hsa_circ_156116,RMVar_hsa_circ_156114,RMVar_hsa_circ_156112 54655 RMVar_ID_54655 Human_SNP_ID_816687736 A-to-I Human chr12 + 121777222 121777222 121777222 TCGATCTCTTGACCTTGTGATCTGCCTGCCTCAGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG TCGATCTCTTGACCTTGTGATCTGCCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAG A G TMEM120B Ensembl:ENSG00000188735 Protein coding intron GSE38233 cultured B-cells chr12:121777221..121777222 24183664 RNA-Seq:(High) rs73413716 Functional Loss SNV ICGC 33..33 33 ESCA 1 - 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 54656 RMVar_ID_54656 Human_SNP_ID_816697904 A-to-I Human chr12 - 94362516 94362516 94362516 TCTCTTGCCTCAGCCTCCTGAGCAGCTGGATTACAGGTGTGTGCCACCATGCCTGGCTAATTTAT TCTCTTGCCTCAGCCTCCTGAGCAGCTGGATTTCAGGTGTGTGCCACCATGCCTGGCTAATTTAT T A CEP83 Ensembl:ENSG00000173588 Protein coding intron GSE100210 HepG2 cell line chr12:94362515..94362516 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue RMVar_hsa_circ_89775,RMVar_hsa_circ_332671,RMVar_hsa_circ_354440,RMVar_hsa_circ_158800,RMVar_hsa_circ_336067,RMVar_hsa_circ_158801,RMVar_hsa_circ_29915,RMVar_hsa_circ_158802,RMVar_hsa_circ_71167,RMVar_hsa_circ_50470,RMVar_hsa_circ_58189,RMVar_hsa_circ_107227,RMVar_hsa_circ_158806,RMVar_hsa_circ_341652,RMVar_hsa_circ_352567,RMVar_hsa_circ_61935,RMVar_hsa_circ_35292,RMVar_hsa_circ_70121,RMVar_hsa_circ_72243 54657 RMVar_ID_54657 Human_SNP_ID_816709438 A-to-I Human chr12 + 27421392 27421391 27421392 ATATGGTGAAACCCCGTTTCTACTAAAAATACAAAAAAAATTACCCAGGCACTCACTCTTGAGGT ATATGGTGAAACCCCGTTTCTACTAAAAATAC_AAAAAAATTACCCAGGCACTCACTCTTGAGGT CA C ARNTL2 Ensembl:ENSG00000029153 Protein coding 3'UTR GSE123020:GSM3490832,GSM3490833,GSM3490834 esophageal squamous carcinoma cells,KYSE180 cell line chr12:27421392..27421393 32596459 RNA-Seq:(High) rs752772526 Functional Loss DEL ICGC 33..33 33 PAAD 1 - RMVar_hsa_circ_117233,RMVar_hsa_circ_155466,RMVar_hsa_circ_155484,RMVar_hsa_circ_155491,RMVar_hsa_circ_155492 54658 RMVar_ID_54658 Human_SNP_ID_816757726 A-to-I Human chr12 - 64338772 64338772 64338772 TTGCTCTCACCATGGCTCTCAGCAATGCTGACATGCAAAAGCAGATAAAGCATATGATGGCTTTC TTGCTCTCACCATGGCTCTCAGCAATGCTGACGTGCAAAAGCAGATAAAGCATATGATGGCTTTC T C AC135279.3,C12orf56 Ensembl:ENSG00000256293,Ensembl:ENSG00000185306 Pseudogene,Protein coding exon,intron GSE100210 HepG2 cell line chr12:64338771..64338772 29129909 RNA-Seq:(High) rs878989790 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 haematopoietic and lymphoid tissue Human_miRNA_ID_1853119 RMVar_hsa_circ_53606 54659 RMVar_ID_54659 Human_SNP_ID_816793865 A-to-I Human chr12 - 56668116 56668112 56668116 TGAAATCTACTCTTTTAACAGACTATTTATTTATTTTTTTGAGGCAGAGTTTTGCTCTTGTTGCC TGAAATCTACTCTTTTAACAGACTATTTATTT____TTTTGAGGCAGAGTTTTGCTCTTGTTGCC AAAAT A PTGES3 Ensembl:ENSG00000110958 Protein coding intron GSE100210 HepG2 cell line chr12:56668115..56668116 29129909 RNA-Seq:(High) rs761630579 Functional Loss DEL ICGC 33..36 33 BRCA 1 - Human_RBP_ID_9691740,Human_RBP_ID_11990393,Human_RBP_ID_24985427 RMVar_hsa_circ_157452,RMVar_hsa_circ_31608,RMVar_hsa_circ_265226,RMVar_hsa_circ_374821,RMVar_hsa_circ_265153,RMVar_hsa_circ_269992,RMVar_hsa_circ_349993,RMVar_hsa_circ_157451,RMVar_hsa_circ_271848,RMVar_hsa_circ_157453 54660 RMVar_ID_54660 Human_SNP_ID_816832961 A-to-I Human chr12 + 1701304 1701304 1701304 TTTACACCACTGTGCCCAGCTAATATTTGTATATTTTGTAGAGATTGGGTTTCGCCTGTTGCCCA TTTACACCACTGTGCCCAGCTAATATTTGTATGTTTTGTAGAGATTGGGTTTCGCCTGTTGCCCA A G ADIPOR2 Ensembl:ENSG00000006831 Protein coding intron GSE100210 HepG2 cell line chr12:1701303..1701304 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_11893509,Human_RBP_ID_17560975 54661 RMVar_ID_54661 Human_SNP_ID_816929608 A-to-I Human chr12 - 42432558 42432558 42432558 TGGAGGATTTTATTCAGGTTTCTAAGAATCTCACTGGAAAAGTAATTGGAAAAAATGGCAAAGTT TGGAGGATTTTATTCAGGTTTCTAAGAATCTCGCTGGAAAAGTAATTGGAAAAAATGGCAAAGTT T C AC079601.3 Ensembl:ENSG00000257376 Pseudogene intron GSE100210 HepG2 cell line chr12:42432557..42432558 29129909 RNA-Seq:(High) rs1374735687 Functional Loss SNV ICGC 33..33 33 LUSC 1 - 54662 RMVar_ID_54662 Human_SNP_ID_816942817 A-to-I Human chr12 + 19724230 19724230 19724230 GAAGCTGGACCCCTTCCTTACACTGTATACAAAATCAACTCAAGAGGGTTAAGGACTTAAATGTA GAAGCTGGACCCCTTCCTTACACTGTATACAATATCAACTCAAGAGGGTTAAGGACTTAAATGTA A T - - Other Unknown GSE100210 HepG2 cell line chr12:19724230..19724231 29129909 RNA-Seq:(High) rs1315762582 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 54663 RMVar_ID_54663 Human_SNP_ID_816953161 A-to-I Human chr12 - 6576428 6576428 6576428 CACCTGTAGTTCCAGCTACTTAGGAGGCTGCAATGAGCCTAGATTGTGCCATTGCACTCCAGCCT CACCTGTAGTTCCAGCTACTTAGGAGGCTGCAGTGAGCCTAGATTGTGCCATTGCACTCCAGCCT T C CHD4,AC006064.6 Ensembl:ENSG00000111642,Ensembl:ENSG00000285238 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line chr12:6576427..6576428 29129909 RNA-Seq:(High) rs867438885 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_8382008,Human_RBP_ID_12010440 RMVar_hsa_circ_100510,RMVar_hsa_circ_102778,RMVar_hsa_circ_154580,RMVar_hsa_circ_154581 54664 RMVar_ID_54664 Human_SNP_ID_816965302 A-to-I Human chr12 + 64450288 64450288 64450288 ATCCTCCTGCCTCAGCATCCAGACTAGCTGTGATTACAGGTGTGCACCACCACACCCAGCTACAT ATCCTCCTGCCTCAGCATCCAGACTAGCTGTGGTTACAGGTGTGCACCACCACACCCAGCTACAT A G XPOT Ensembl:ENSG00000184575 Protein coding 3'UTR GSE100210 HepG2 cell line chr12:64450287..64450288 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 2 breast Human_RBP_ID_26418882 Human_miRNA_ID_706825,Human_miRNA_ID_714074,Human_miRNA_ID_1515920 54665 RMVar_ID_54665 Human_SNP_ID_816973100 A-to-I Human chr12 + 107715509 107715509 107715509 AAATAGCACCATGAGAAAGATAGACCTGTAATAAATTCACACATTGGACTTATGTTGGACATGAA AAATAGCACCATGAGAAAGATAGACCTGTAATGAATTCACACATTGGACTTATGTTGGACATGAA A G - - Other Unknown GSE100210 HepG2 cell line chr12:107715508..107715509 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 54666 RMVar_ID_54666 Human_SNP_ID_816993220 A-to-I Human chr12 + 110461118 110461118 110461118 CTATGGAGTGGGCTTCAAGAAGCGTGCCCCTCAGGCACTCAAAGAGATTCAGAAATTTGCCATGA CTATGGAGTGGGCTTCAAGAAGCGTGCCCCTCGGGCACTCAAAGAGATTCAGAAATTTGCCATGA A G RPL31P49 Ensembl:ENSG00000241680 Pseudogene exon GSE100210 HepG2 cell line chr12:110461117..110461118 29129909 RNA-Seq:(High) rs878920872 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 8 haematopoietic and lymphoid tissue Human_miRNA_ID_1842503,Human_miRNA_ID_1855032,Human_miRNA_ID_1871477 54667 RMVar_ID_54667 Human_SNP_ID_817033143 A-to-I Human chr12 + 19578424 19578424 19578424 TAGCAATGGGTTTTTGCCATGTTGTCTAGGCTAGTCTGGAACTCCTGGGCTCAAGCGATTTGCCT TAGCAATGGGTTTTTGCCATGTTGTCTAGGCTGGTCTGGAACTCCTGGGCTCAAGCGATTTGCCT A G AEBP2 Ensembl:ENSG00000139154 Protein coding intron GSE100210 HepG2 cell line chr12:19578423..19578424 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_11899620 54668 RMVar_ID_54668 Human_SNP_ID_817050842 A-to-I Human chr12 + 101307427 101307427 101307427 TTTACGGGGTCTCACTCTGTCACCTAGACTGGAATGCAGTGGCGTGATTTCGGCTCACTGCAGTC TTTACGGGGTCTCACTCTGTCACCTAGACTGGGATGCAGTGGCGTGATTTCGGCTCACTGCAGTC A G UTP20 Ensembl:ENSG00000120800 Protein coding intron GSE100210 HepG2 cell line chr12:101307427..101307428 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - RMVar_hsa_circ_28847,RMVar_hsa_circ_67587,RMVar_hsa_circ_110546,RMVar_hsa_circ_159239,RMVar_hsa_circ_101035,RMVar_hsa_circ_18254,RMVar_hsa_circ_359899,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_127748,RMVar_hsa_circ_159246 54669 RMVar_ID_54669 Human_SNP_ID_817054937 A-to-I Human chr12 - 79798517 79798517 79798517 AATCCCAAAGAAAAGCAAGATCTAGACAAGCAAGACAATCTAGAAGATCAACACAGGTATAGTTA AATCCCAAAGAAAAGCAAGATCTAGACAAGCATGACAATCTAGAAGATCAACACAGGTATAGTTA T A PPP1R12A Ensembl:ENSG00000058272 Protein coding CDS GSE100210 HepG2 cell line chr12:79798516..79798517 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_877535,Human_RBP_ID_1478246,Human_RBP_ID_1802200,Human_RBP_ID_5555749 Human_Splice_Rec_1402376,Human_Splice_Rec_1402377,Human_Splice_Rec_1402424,Human_Splice_Rec_1402425,Human_Splice_Rec_1402474,Human_Splice_Rec_1402475,Human_Splice_Rec_1402598,Human_Splice_Rec_1402599,Human_Splice_Rec_1402644,Human_Splice_Rec_1402645,Human_Splice_Rec_1402677,Human_Splice_Rec_1402696,Human_Splice_Rec_1402697,Human_Splice_Rec_1402726,Human_Splice_Rec_1402727,Human_Splice_Rec_1402730,Human_Splice_Rec_1402731,Human_Splice_Rec_1402744,Human_Splice_Rec_1402745,Human_Splice_Rec_1402760,Human_Splice_Rec_1402761 Human_miRNA_ID_1264419,Human_miRNA_ID_2239652,Human_miRNA_ID_2611398,Human_miRNA_ID_2704670,Human_miRNA_ID_3016944 RMVar_hsa_circ_64063,RMVar_hsa_circ_158510,RMVar_hsa_circ_49883,RMVar_hsa_circ_41937,RMVar_hsa_circ_60026,RMVar_hsa_circ_33394,RMVar_hsa_circ_78609,RMVar_hsa_circ_281167,RMVar_hsa_circ_158514,RMVar_hsa_circ_73583,RMVar_hsa_circ_17268,RMVar_hsa_circ_60671,RMVar_hsa_circ_158515,RMVar_hsa_circ_70468 54670 RMVar_ID_54670 Human_SNP_ID_817186877 A-to-I Human chr12 - 122509962 122509962 122509962 CAAAAATTAGCCAGGCGTGGTTGTGTGTGCCTATAGTCCCAGCTACTCAGGAGGCTTGAACTCGG CAAAAATTAGCCAGGCGTGGTTGTGTGTGCCTGTAGTCCCAGCTACTCAGGAGGCTTGAACTCGG T C RSRC2 Ensembl:ENSG00000111011 Protein coding intron GSE38233 cultured B-cells chr12:122509961..122509962 24183664 RNA-Seq:(High) rs777591321 Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 2 liver RMVar_hsa_circ_327177,RMVar_hsa_circ_66156,RMVar_hsa_circ_304157,RMVar_hsa_circ_324267,RMVar_hsa_circ_356319,RMVar_hsa_circ_161081,RMVar_hsa_circ_161082 54671 RMVar_ID_54671 Human_SNP_ID_817240648 A-to-I Human chr12 - 46261276 46261276 46261276 AACAGTCAAGCAGGTTCTCAACTGGAACAATTATGTCCCTCTCCCTGCCCCCAGGAGGTATTTGG AACAGTCAAGCAGGTTCTCAACTGGAACAATTGTGTCCCTCTCCCTGCCCCCAGGAGGTATTTGG T C SLC38A1 Ensembl:ENSG00000111371 Protein coding intron GSE100210 HepG2 cell line chr12:46261275..46261276 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - Human_RBP_ID_26777277 Human_miRNA_ID_2351821,Human_miRNA_ID_3047369 RMVar_hsa_circ_156089,RMVar_hsa_circ_77941,RMVar_hsa_circ_117672,RMVar_hsa_circ_156109 54672 RMVar_ID_54672 Human_SNP_ID_817258406 A-to-I Human chr12 - 26978058 26978058 26978058 AGGATCTCTTTCTGTCACCCATGCTGGACTGCAGTGACACTATCATAGCTCACTGCAACCTCAAA AGGATCTCTTTCTGTCACCCATGCTGGACTGCGGTGACACTATCATAGCTCACTGCAACCTCAAA T C TM7SF3 Ensembl:ENSG00000064115 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line chr12:26978057..26978058 29129909,31158229 RNA-Seq:(High) rs1179839993 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue Human_RBP_ID_11912918 Human_Splice_Rec_1349304 RMVar_hsa_circ_155432,RMVar_hsa_circ_91077,RMVar_hsa_circ_113847,RMVar_hsa_circ_123334,RMVar_hsa_circ_155433,RMVar_hsa_circ_155434,RMVar_hsa_circ_265575,RMVar_hsa_circ_155435,RMVar_hsa_circ_155436,RMVar_hsa_circ_266182,RMVar_hsa_circ_266379,RMVar_hsa_circ_51618 54673 RMVar_ID_54673 Human_SNP_ID_817273888 A-to-I Human chr12 - 38811756 38811756 38811756 CAGATCTTCCTGCCTCAGCCTCCCAAATAGCTAGGACTACAGGTGTGCACCACCACACCCAGCTA CAGATCTTCCTGCCTCAGCCTCCCAAATAGCTGGGACTACAGGTGTGCACCACCACACCCAGCTA T C CPNE8 Ensembl:ENSG00000139117 Protein coding intron GSE100210 HepG2 cell line chr12:38811755..38811756 29129909 RNA-Seq:(High) rs569346190 Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_108827,RMVar_hsa_circ_155822,RMVar_hsa_circ_11593,RMVar_hsa_circ_39635,RMVar_hsa_circ_92273,RMVar_hsa_circ_155828,RMVar_hsa_circ_55755 54674 RMVar_ID_54674 Human_SNP_ID_817305671 A-to-I Human chr12 - 15934 15931 15934 GCAGCATGAAGGAGCGAAAGCTGGAGAAGAAGAAGCAGAAGGAGCAGGAGCAAGGTGAGCGGGCC GCAGCATGAAGGAGCGAAAGCTGGAGAAGAAG___CAGAAGGAGCAGGAGCAAGGTGAGCGGGCC GCTT G WASH8P Ensembl:ENSG00000226210 Pseudogene exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr12:15933..15934 30559470 RNA-Seq:(High) - Functional Loss DEL TCGA 33..35 33 CHOL 1 - Human_Splice_Rec_1319493 54675 RMVar_ID_54675 Human_SNP_ID_817308783 A-to-I Human chr12 + 64450387 64450387 64450387 CCCAGTCTGGTCTCAAACTCCCGGCCTCAAGCAATCCTCCCACTGGCCTCACAATGTTGGGATTA CCCAGTCTGGTCTCAAACTCCCGGCCTCAAGCGATCCTCCCACTGGCCTCACAATGTTGGGATTA A G XPOT Ensembl:ENSG00000184575 Protein coding 3'UTR GSE38233 cultured B-cells chr12:64450386..64450387 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_425555,Human_RBP_ID_23569527,Human_RBP_ID_26421506 54676 RMVar_ID_54676 Human_SNP_ID_817345823 A-to-I Human chr12 + 64450281 64450281 64450281 TCTACCAATCCTCCTGCCTCAGCATCCAGACTAGCTGTGATTACAGGTGTGCACCACCACACCCA TCTACCAATCCTCCTGCCTCAGCATCCAGACTGGCTGTGATTACAGGTGTGCACCACCACACCCA A G XPOT Ensembl:ENSG00000184575 Protein coding 3'UTR GSE38233;GSE100210;GSE107867;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;ASD brains,Fragile X samples from UC Davis FXTAS brain repository;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line;Bronchiolar epithelium,BERP35T4 cell line chr12:64450280..64450281 24183664,29129909,30559470,31158229,31158229,31158229 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_425553,Human_RBP_ID_26418882 54677 RMVar_ID_54677 Human_SNP_ID_817347696 A-to-I Human chr12 - 112101743 112101741 112101743 TTTTTTTGATAGATTTTTTAAGATGCAGTCTCACTCTGTCACCTGGGCTGGAGTGCAATGGCGTG TTTTTTTGATAGATTTTTTAAGATGCAGTCTC__TCTGTCACCTGGGCTGGAGTGCAATGGCGTG AGT A NAA25 Ensembl:ENSG00000111300 Protein coding intron GSE100210 HepG2 cell line chr12:112101742..112101743 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 33..34 33 LICA 1 - 54678 RMVar_ID_54678 Human_SNP_ID_817349873 A-to-I Human chr12 + 65454015 65454015 65454015 CAAGTCTAGTGGAATGTTAAGGTCGGCATGATAGCTCAAGCCTGTAATCCCATACTTTGAGAGGG CAAGTCTAGTGGAATGTTAAGGTCGGCATGATGGCTCAAGCCTGTAATCCCATACTTTGAGAGGG A G MSRB3 Ensembl:ENSG00000174099 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line chr12:65454014..65454015 31158229 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 18 haematopoietic and lymphoid tissue 54679 RMVar_ID_54679 Human_SNP_ID_817351662 A-to-I Human chr12 - 42432893 42432893 42432893 GACACTGTCTGCCAGTGAAGCAACTGTGAAGAAAGTAAACATCTTGAGTGACATGCGTTTGTGAA GACACTGTCTGCCAGTGAAGCAACTGTGAAGAGAGTAAACATCTTGAGTGACATGCGTTTGTGAA T C AC079601.3 Ensembl:ENSG00000257376 Pseudogene intron GSE100210 HepG2 cell line chr12:42432892..42432893 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 28 haematopoietic and lymphoid tissue Human_RBP_ID_8248171 54680 RMVar_ID_54680 Human_SNP_ID_817371344 A-to-I Human chr12 - 49069170 49069170 49069170 TGGGGTCTCCTTTGGTCCTGGGCCACAGTCCGAAAGGACAGAGGATGTGAATGTGGATGGATGAT TGGGGTCTCCTTTGGTCCTGGGCCACAGTCCGGAAGGACAGAGGATGTGAATGTGGATGGATGAT T C RHEBL1 Ensembl:ENSG00000167550 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr12:49069170..49069171 30559470 RNA-Seq:(High) - Functional Loss SNV TCGA 33..33 33 UCEC 1 - Human_RBP_ID_22644765 Human_Splice_Rec_1363954 RMVar_hsa_circ_25576,RMVar_hsa_circ_127854,RMVar_hsa_circ_156283 54681 RMVar_ID_54681 Human_SNP_ID_817383693 A-to-I Human chr12 - 53178216 53178216 53178216 CATTGGCCTCGGCCTCCTAGAGTGCTAGGATTACAGGATTGAGCCACCATGCCTGGCCGGATATG CATTGGCCTCGGCCTCCTAGAGTGCTAGGATTGCAGGATTGAGCCACCATGCCTGGCCGGATATG T C CSAD Ensembl:ENSG00000139631 Protein coding intron GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611830,GSM3611831,GSM3611832 cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T1 cell line chr12:53178215..53178216 24183664,29129909,31158229,31158229 RNA-Seq:(High) rs1032073051 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 5 haematopoietic and lymphoid tissue Human_RBP_ID_11973451,Human_RBP_ID_25024181 54682 RMVar_ID_54682 Human_SNP_ID_817407249 A-to-I Human chr12 + 124913220 124913220 124913220 AACCTCTGCTGATCAGGAGGAATGCCTTCCTTATCTTGGATCTTTGCCTTGACATTCTCGATGGT AACCTCTGCTGATCAGGAGGAATGCCTTCCTTGTCTTGGATCTTTGCCTTGACATTCTCGATGGT A G - - Other Unknown GSE100210 HepG2 cell line chr12:124913219..124913220 29129909 RNA-Seq:(High) rs370055957 Functional Loss SNV ICGC 33..33 33 COCA 1 - 54683 RMVar_ID_54683 Human_SNP_ID_817420789 A-to-I Human chr12 + 54346729 54346729 54346729 AATAAAAAAATTAGCCAGGTGTGGTGGTGCATACCTGTAGTCTCAGCTACTTGGGAGGCTGAGGT AATAAAAAAATTAGCCAGGTGTGGTGGTGCATGCCTGTAGTCTCAGCTACTTGGGAGGCTGAGGT A G COPZ1 Ensembl:ENSG00000111481 Protein coding intron GSE38233 cultured B-cells chr12:54346728..54346729 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 10 haematopoietic and lymphoid tissue 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 54684 RMVar_ID_54684 Human_SNP_ID_817482893 A-to-I Human chr12 - 118143392 118143392 118143392 CTCTAGGACTATTCAGCCTTAAAAAGAAATTCAGACACATGCTACACCAGAGAACCTTGAGAACA CTCTAGGACTATTCAGCCTTAAAAAGAAATTCTGACACATGCTACACCAGAGAACCTTGAGAACA T A - - Other Unknown GSE100210 HepG2 cell line chr12:118143391..118143392 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 2 liver 54685 RMVar_ID_54685 Human_SNP_ID_817483625 A-to-I Human chr12 - 114588420 114588420 114588420 TCAAGTTGCCTCTTTTTGCTACTTCATGCAATAGATTGTCAATGGATTCTGCCTGCTCGGCCACA TCAAGTTGCCTCTTTTTGCTACTTCATGCAATGGATTGTCAATGGATTCTGCCTGCTCGGCCACA T C HSALNG0094220 RNACentral:URS0000EA1A7F lincRNA intron GSE100210 HepG2 cell line chr12:114588419..114588420 29129909 RNA-Seq:(High) rs878875562 Functional Loss SNV ICGC 33..33 33 LAML 2 - 54686 RMVar_ID_54686 Human_SNP_ID_817521539 A-to-I Human chr12 - 48667145 48667145 48667145 AGTTTTGCTCTAGTCTCCCAGGCTGGAGTGCAATGGCGTGATCTCGGCTCACTGCAACCTCCACC AGTTTTGCTCTAGTCTCCCAGGCTGGAGTGCAGTGGCGTGATCTCGGCTCACTGCAACCTCCACC T C KANSL2 Ensembl:ENSG00000139620 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr12:48667144..48667145 24183664,29129909 RNA-Seq:(High) rs559732235 Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 4 oesophagus Human_RBP_ID_12081985 RMVar_hsa_circ_117877,RMVar_hsa_circ_79268,RMVar_hsa_circ_156186,RMVar_hsa_circ_372714,RMVar_hsa_circ_371677,RMVar_hsa_circ_3561,RMVar_hsa_circ_156189,RMVar_hsa_circ_156191,RMVar_hsa_circ_110727,RMVar_hsa_circ_156190,RMVar_hsa_circ_293796,RMVar_hsa_circ_156188,RMVar_hsa_circ_274441,RMVar_hsa_circ_156193,RMVar_hsa_circ_156194 54687 RMVar_ID_54687 Human_SNP_ID_817527090 A-to-I Human chr12 + 49325330 49325330 49325330 CACCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACTGCACCCAGCCATCTATT CACCCGCCTCGGCCTCCCAAAGTGCTGGGATTGCAGGCATGAGCCACTGCACCCAGCCATCTATT A G TROAP Ensembl:ENSG00000135451 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line chr12:49325329..49325330 31158229 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - RMVar_hsa_circ_21287 54688 RMVar_ID_54688 Human_SNP_ID_817576102 A-to-I Human chr12 - 57429655 57429655 57429655 AGAATGGAGTGTAGTGGTTCCTTTTCGGCTCAATGCAACCTCTGCCTCCTGGCCTCAAGCCGTCC AGAATGGAGTGTAGTGGTTCCTTTTCGGCTCAGTGCAACCTCTGCCTCCTGGCCTCAAGCCGTCC T C R3HDM2 Ensembl:ENSG00000179912 Protein coding intron GSE100210 HepG2 cell line chr12:57429654..57429655 29129909 RNA-Seq:(High) rs776246665 Functional Loss SNV COSMIC 33..33 33 meninges atypical 3 brain Human_RBP_ID_11994791,Human_RBP_ID_23306041 Human_miRNA_ID_2273059,Human_miRNA_ID_2445599,Human_miRNA_ID_2446985,Human_miRNA_ID_2475801,Human_miRNA_ID_2961585 RMVar_hsa_circ_93739,RMVar_hsa_circ_157649 54689 RMVar_ID_54689 Human_SNP_ID_817579112 A-to-I Human chr12 - 100009456 100009456 100009456 GAGGCCAAGTACAAGTTGTGCAAAGTGAGAAAAATCTTTGTGGGCACAAAAGGAATCTCTCGTCT GAGGCCAAGTACAAGTTGTGCAAAGTGAGAAAGATCTTTGTGGGCACAAAAGGAATCTCTCGTCT T C RPS4XP1 Ensembl:ENSG00000214203 Pseudogene exon GSE100210 HepG2 cell line chr12:100009455..100009456 29129909 RNA-Seq:(High) rs878998246 Functional Loss SNV ICGC 33..33 33 LAML 2 - 54690 RMVar_ID_54690 Human_SNP_ID_817618316 A-to-I Human chr12 - 7929557 7929557 7929557 AGGAGGCTGAGGTAAGAGGATCACTTGAGCTCAGGAGTTTCAGGTTGCAGTGAGCTATAATTATG AGGAGGCTGAGGTAAGAGGATCACTTGAGCTCGGGAGTTTCAGGTTGCAGTGAGCTATAATTATG T C SLC2A3 Ensembl:ENSG00000059804 Protein coding intron GSE100210 HepG2 cell line chr12:7929556..7929557 29129909 RNA-Seq:(High) rs1266877006 Functional Loss SNV TCGA 33..33 33 UCEC 1 - RMVar_hsa_circ_124122,RMVar_hsa_circ_95032,RMVar_hsa_circ_154727,RMVar_hsa_circ_154726,RMVar_hsa_circ_68152 54691 RMVar_ID_54691 Human_SNP_ID_817621345 A-to-I Human chr12 - 118154577 118154577 118154577 AAATTAGCTGGGCCTGGTGGCACTTACCTGTAATCTCAGCTACTCGGGAGGATGAGGCAGGAGAA AAATTAGCTGGGCCTGGTGGCACTTACCTGTACTCTCAGCTACTCGGGAGGATGAGGCAGGAGAA T G TAOK3 Ensembl:ENSG00000135090 Protein coding intron GSE100210 HepG2 cell line chr12:118154576..118154577 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 4 liver RMVar_hsa_circ_24615,RMVar_hsa_circ_117399,RMVar_hsa_circ_160572,RMVar_hsa_circ_160573 54692 RMVar_ID_54692 Human_SNP_ID_817626831 A-to-I Human chr12 - 8226067 8226067 8226067 CTTAGAGTGGGCTGTGCAGATAGACCTTTCCGAGTCATGTAATTGGATTAAGTTAATTGTAATTA CTTAGAGTGGGCTGTGCAGATAGACCTTTCCGGGTCATGTAATTGGATTAAGTTAATTGTAATTA T C FAM90A1 Ensembl:ENSG00000171847 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr12:8226066..8226067 30559470 RNA-Seq:(High) rs796442698 Functional Loss SNV ICGC 33..33 33 LUSC 1 - 54693 RMVar_ID_54693 Human_SNP_ID_842951554 A-to-I Human chr21 - 31191427 31191412 31191428 GCCACAGGCTGGACACAGAGGGTCACACCTGTAATCCCAGCATTTTGGGAGGCCGAGGTGGGCAG GCCACAGGCTGGACACAGAGGGTCACACCTG________________GGAGGCCGAGGTGGGCAG CCAAAATGCTGGGATTA C TIAM1 Ensembl:ENSG00000156299 Protein coding intron GSE107867 ASD brains,cerebellum chr21:31191426..31191427 30559470 RNA-Seq:(High) - Functional Loss DEL ICGC 32..47 33 BRCA 1 - RMVar_hsa_circ_865,RMVar_hsa_circ_65855,RMVar_hsa_circ_47839,RMVar_hsa_circ_17084,RMVar_hsa_circ_46931,RMVar_hsa_circ_59467,RMVar_hsa_circ_73797,RMVar_hsa_circ_354160,RMVar_hsa_circ_362424,RMVar_hsa_circ_326679,RMVar_hsa_circ_364165,RMVar_hsa_circ_275879,RMVar_hsa_circ_309327,RMVar_hsa_circ_29232,RMVar_hsa_circ_289169,RMVar_hsa_circ_363180,RMVar_hsa_circ_369084,RMVar_hsa_circ_322800,RMVar_hsa_circ_66226,RMVar_hsa_circ_38671,RMVar_hsa_circ_211707,RMVar_hsa_circ_268856,RMVar_hsa_circ_306584,RMVar_hsa_circ_358311,RMVar_hsa_circ_296920,RMVar_hsa_circ_42256 54694 RMVar_ID_54694 Human_SNP_ID_842967018 A-to-I Human chr21 - 44852737 44852737 44852737 AACTGGAAGTAGACTCAGGAGCGAGTTTTTCAATAAGAACTTAACCAGCCTCCTTGCTAGTATCT AACTGGAAGTAGACTCAGGAGCGAGTTTTTCAGTAAGAACTTAACCAGCCTCCTTGCTAGTATCT T C PTTG1IP Ensembl:ENSG00000183255 Protein coding intron GSE38233 cultured B-cells chr21:44852736..44852737 24183664 RNA-Seq:(High) rs1344110 Functional Loss SNV ICGC 33..33 33 ESCA 1 - GWAS_ID_636,GWAS_ID_637,GWAS_ID_638,GWAS_ID_639,GWAS_ID_640,GWAS_ID_641 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 54695 RMVar_ID_54695 Human_SNP_ID_842997228 A-to-I Human chr21 - 42843575 42843575 42843575 AGCAAGAATCTGTCTTAAAAAAAAAAAAAATTAGCCAGGTGTGGTGGCACATGCCTGTAGTCCCA AGCAAGAATCTGTCTTAAAAAAAAAAAAAATTTGCCAGGTGTGGTGGCACATGCCTGTAGTCCCA T A WDR4 Ensembl:ENSG00000160193 Protein coding intron GSE100210 HepG2 cell line chr21:42843574..42843575 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_23010155,Human_RBP_ID_25645660 RMVar_hsa_circ_83292,RMVar_hsa_circ_87955,RMVar_hsa_circ_102409,RMVar_hsa_circ_86509,RMVar_hsa_circ_212430,RMVar_hsa_circ_212432,RMVar_hsa_circ_80464,RMVar_hsa_circ_212433,RMVar_hsa_circ_212431,RMVar_hsa_circ_212429 54696 RMVar_ID_54696 Human_SNP_ID_843055743 A-to-I Human chr21 + 33405923 33405923 33405923 CGTGATGGTACACACCTGTGTCCCAGCTACTCAGGAGGCTGAAGCCGAAGAATCACTTAAACTCA CGTGATGGTACACACCTGTGTCCCAGCTACTCGGGAGGCTGAAGCCGAAGAATCACTTAAACTCA A G IFNGR2 Ensembl:ENSG00000159128 Protein coding intron GSE38233 cultured B-cells chr21:33405922..33405923 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - 54697 RMVar_ID_54697 Human_SNP_ID_843058360 A-to-I Human chr21 + 33355762 33355762 33355762 TTACAGGCCCGGGCACGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGCAG TTACAGGCCCGGGCACGGTGGCTCACACCTGTGATCCCAGCACTTTGGGAGGCTGAGGCAGGCAG A G IFNAR1 Ensembl:ENSG00000142166 Protein coding 3'UTR GSE100210;GSE99789 HepG2 cell line;esophageal squamous carcinoma cells,EC109 chr21:33355761..33355762;chr21:33355762..33355763 29129909,29796672 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue Human_miRNA_ID_1359256 54698 RMVar_ID_54698 Human_SNP_ID_843086757 A-to-I Human chr21 + 36969599 36969599 36969599 ACCACAGACTAGGGATTTTTTTTTTTTTTTTTAGATGAAGTCTCACTTGCCCAGGTTGGAGTGCA ACCACAGACTAGGGATTTTTTTTTTTTTTTTTGGATGAAGTCTCACTTGCCCAGGTTGGAGTGCA A G AP000704.2 Ensembl:ENSG00000224790 lincRNA exon GSE100210 HepG2 cell line chr21:36969598..36969599 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 3 prostate Human_Splice_Rec_2119907 54699 RMVar_ID_54699 Human_SNP_ID_843108564 A-to-I Human chr21 - 34797885 34797885 34797885 TAGATGCCAATAGCATCCCCCTCACCCCAGTTAGGACAATAAAAAATGTTTCCAGACATTGCCAA TAGATGCCAATAGCATCCCCCTCACCCCAGTTGGGACAATAAAAAATGTTTCCAGACATTGCCAA T C RUNX1 Ensembl:ENSG00000159216 Protein coding intron GSE100210 HepG2 cell line chr21:34797884..34797885 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 5 haematopoietic and lymphoid tissue RMVar_hsa_circ_211970,RMVar_hsa_circ_105995,RMVar_hsa_circ_76660,RMVar_hsa_circ_211971 54700 RMVar_ID_54700 Human_SNP_ID_843131468 A-to-I Human chr21 + 29028687 29028687 29028687 TGAACTCCTGACCTCAAGTGATCCGCTTCCTCAGCATCCCAAAGTGCTGGGATTACAGGCGTGAG TGAACTCCTGACCTCAAGTGATCCGCTTCCTCCGCATCCCAAAGTGCTGGGATTACAGGCGTGAG A C USP16 Ensembl:ENSG00000156256 Protein coding intron GSE100210 HepG2 cell line chr21:29028686..29028687 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_14222472 RMVar_hsa_circ_12482,RMVar_hsa_circ_312965,RMVar_hsa_circ_353590,RMVar_hsa_circ_361454,RMVar_hsa_circ_362700,RMVar_hsa_circ_363615,RMVar_hsa_circ_354831,RMVar_hsa_circ_335105,RMVar_hsa_circ_68386,RMVar_hsa_circ_70161,RMVar_hsa_circ_211650,RMVar_hsa_circ_9814 54701 RMVar_ID_54701 Human_SNP_ID_843145820 A-to-I Human chr21 + 32776423 32776423 32776423 AAAAATATTCTATATACATTAGCTGATGTCTTAGTCCATTTGGGCTGCTACAACAAAATACCATT AAAAATATTCTATATACATTAGCTGATGTCTTCGTCCATTTGGGCTGCTACAACAAAATACCATT A C C21orf62-AS1 Ensembl:ENSG00000205930 lincRNA intron GSE100210 HepG2 cell line chr21:32776422..32776423 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 54702 RMVar_ID_54702 Human_SNP_ID_843148825 A-to-I Human chr21 + 14094638 14094638 14094638 TGTGAGGCTGAGGCAGAGGATTGCTTGAACCCAGGAGTGCAAGGCTGCATTGAGCTATAATTGTG TGTGAGGCTGAGGCAGAGGATTGCTTGAACCCTGGAGTGCAAGGCTGCATTGAGCTATAATTGTG A T AP001347.1 Ensembl:ENSG00000224905 lincRNA intron GSE100210 HepG2 cell line chr21:14094637..14094638 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_8261473,Human_RBP_ID_14186632 RMVar_hsa_circ_211444 54703 RMVar_ID_54703 Human_SNP_ID_843163354 A-to-I Human chr21 - 36050705 36050705 36050705 TTATCTCGAGCCAAGAAAACAGCTTTACCTCTATGACCCCGCGTATTCTTTACTACCATTGGGAA TTATCTCGAGCCAAGAAAACAGCTTTACCTCTGTGACCCCGCGTATTCTTTACTACCATTGGGAA T C SETD4 Ensembl:ENSG00000185917 Protein coding intron GSE107867 ASD brains,temporal_cortex chr21:36050704..36050705 30559470 RNA-Seq:(High) rs1395637836 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 16 haematopoietic and lymphoid tissue RMVar_hsa_circ_114584,RMVar_hsa_circ_211978,RMVar_hsa_circ_43052,RMVar_hsa_circ_88990,RMVar_hsa_circ_125722,RMVar_hsa_circ_211980,RMVar_hsa_circ_211982 54704 RMVar_ID_54704 Human_SNP_ID_843248070 A-to-I Human chr21 + 33358771 33358771 33358771 CTATAATCTCAGCACTTTTGGGAGGCCAAGACAGGAGGATCACTTCAGGCCAGGAGTTCAAGATC CTATAATCTCAGCACTTTTGGGAGGCCAAGACTGGAGGATCACTTCAGGCCAGGAGTTCAAGATC A T IFNAR1 Ensembl:ENSG00000142166 Protein coding 3'UTR GSE38233 cultured B-cells chr21:33358770..33358771 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_7039404,Human_RBP_ID_14254831 54705 RMVar_ID_54705 Human_SNP_ID_843285908 A-to-I Human chr21 + 17593744 17593744 17593744 ACGACATAAAATAGATTTCCTTGTATATAAATAACTTACATACGCTCCATAAAGTAAATTCTCAA ACGACATAAAATAGATTTCCTTGTATATAAATGACTTACATACGCTCCATAAAGTAAATTCTCAA A G - - Other Unknown GSE100210 HepG2 cell line chr21:17593744..17593745 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 UCEC,endometrium endometrioid_carcinoma 4 uterus Human_RBP_ID_569830 54706 RMVar_ID_54706 Human_SNP_ID_843361332 A-to-I Human chr21 + 33261237 33261237 33261237 TTTTGCATTTTTAGTAGAGATGGGGTTTTGCTATGTTGGCCAGGCTGGTCTTGAACTCCTGACTT TTTTGCATTTTTAGTAGAGATGGGGTTTTGCTCTGTTGGCCAGGCTGGTCTTGAACTCCTGACTT A C IFNAR2,AP000295.1 Ensembl:ENSG00000159110,Ensembl:ENSG00000249624 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells chr21:33261236..33261237 24183664 RNA-Seq:(High) rs1019183676 Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_211824,RMVar_hsa_circ_211825,RMVar_hsa_circ_211823,RMVar_hsa_circ_117901,RMVar_hsa_circ_211832,RMVar_hsa_circ_211834,RMVar_hsa_circ_120412 54707 RMVar_ID_54707 Human_SNP_ID_843370371 A-to-I Human chr21 - 33551628 33551628 33551628 GAGCTGGTTGCTAACATCTGGGAGTCCATGGAACTGGTTGCTAACATCTGGGAGTCCATAGTGCT GAGCTGGTTGCTAACATCTGGGAGTCCATGGAGCTGGTTGCTAACATCTGGGAGTCCATAGTGCT T C - - Other Unknown GSE56152 embryonic stem cells,wild type chr21:33551627..33551628 25708366 RNA-Seq:(High) rs200724919 Functional Loss SNV ICGC,COSMIC 33..33 33 liver neoplasm,CHOL,endometrium endometrioid_carcinoma,urinary_tract transitional_cell_carcinoma 25 uterus,liver,urinary tract GWAS_ID_4334 54708 RMVar_ID_54708 Human_SNP_ID_843373040 A-to-I Human chr21 - 31463613 31463613 31463613 AGGTCTCGTCATGTTGGCCAGGCTGGTCTCGAACTCCTTACCTCAGGTGATCCGTCTGCCTCGGC AGGTCTCGTCATGTTGGCCAGGCTGGTCTCGAGCTCCTTACCTCAGGTGATCCGTCTGCCTCGGC T C TIAM1 Ensembl:ENSG00000156299 Protein coding intron GSE107867 ASD brains,cerebellum chr21:31463612..31463613 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_368860,RMVar_hsa_circ_341353 54709 RMVar_ID_54709 Human_SNP_ID_843496983 A-to-I Human chr21 + 42727543 42727542 42727543 TTTGTAGAGATGGAGATCTCTCTTTGTTCCCCAGGCTGGTCTCAAACTCCTGGGCTCAAGCAACC TTTGTAGAGATGGAGATCTCTCTTTGTTCCCC_GGCTGGTCTCAAACTCCTGGGCTCAAGCAACC CA C PDE9A Ensembl:ENSG00000160191 Protein coding intron GSE100210 HepG2 cell line chr21:42727542..42727543 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 33..33 33 PRAD 1 - 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 54710 RMVar_ID_54710 Human_SNP_ID_843498591 A-to-I Human chr21 + 33551013 33551013 33551013 TTGTCGGGGCAGCCTGTGGCAACTGGGGCACTAGAGTTGCCTGGGCCGCTCATGGCAGCTGGGGC TTGTCGGGGCAGCCTGTGGCAACTGGGGCACTGGAGTTGCCTGGGCCGCTCATGGCAGCTGGGGC A G SON Ensembl:ENSG00000159140 Protein coding CDS GSE38233;GSE100210;GSE107867;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;HepG2 cell line;ASD brains,temporal_cortex;esophageal squamous carcinoma cells,KYSE180 cell line chr21:33551012..33551013 24183664,29129909,30559470,32596459 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 5 haematopoietic and lymphoid tissue Human_RBP_ID_5240579,Human_RBP_ID_5503939,Human_RBP_ID_8541265,Human_RBP_ID_8858727,Human_RBP_ID_9299247,Human_RBP_ID_9354192,Human_RBP_ID_14258941,Human_RBP_ID_18463767,Human_RBP_ID_22083138,Human_RBP_ID_23007238,Human_RBP_ID_26788896 RMVar_hsa_circ_78630,RMVar_hsa_circ_121649,RMVar_hsa_circ_211887,RMVar_hsa_circ_89632,RMVar_hsa_circ_211889,RMVar_hsa_circ_211890 54711 RMVar_ID_54711 Human_SNP_ID_843583896 A-to-I Human chr21 - 44047011 44047011 44047011 AAATGGCTGGCAGTAAGGTGGGAAAGGACTCCAGAAAGGCCAAGACAAAGGCGGTTTCCCGCTCG AAATGGCTGGCAGTAAGGTGGGAAAGGACTCCGGAAAGGCCAAGACAAAGGCGGTTTCCCGCTCG T C H2AZP1 Ensembl:ENSG00000213440 Pseudogene exon GSE100210 HepG2 cell line chr21:44047010..44047011 29129909 RNA-Seq:(High) rs1239152346 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 3 haematopoietic and lymphoid tissue 54712 RMVar_ID_54712 Human_SNP_ID_843590992 A-to-I Human chr21 - 8987106 8987106 8987106 ACCCCTCGAGCGCGGCCGACCGCAGCCGGGACACACGCGCGGGGCCTCACCGCCGCCGGCGGCAC ACCCCTCGAGCGCGGCCGACCGCAGCCGGGACGCACGCGCGGGGCCTCACCGCCGCCGGCGGCAC T C lnc-KCNE1B-10,lnc-KCNE1B-3,lnc-KCNE1B-3:2 RNACentral:URS00004687BF,RNACentral:URS0000D58B87,RNACentral:URS0000D592AB lincRNA,lincRNA,lincRNA intron,intron,intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr21:8987105..8987106 30559470 RNA-Seq:(High) rs560916630 Functional Loss SNV ICGC 33..33 33 COCA 3 - 54713 RMVar_ID_54713 Human_SNP_ID_843650746 A-to-I Human chr21 - 31689741 31689741 31689741 TTTTTTTAGTAGAGAAGGGGTTTCACCATGTTAGGCTGGCCTCGAACTCCTGACCTCAGGTGATC TTTTTTTAGTAGAGAAGGGGTTTCACCATGTTGGGCTGGCCTCGAACTCCTGACCTCAGGTGATC T C SCAF4 Ensembl:ENSG00000156304 Protein coding intron GSE100210 HepG2 cell line chr21:31689740..31689741 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_14236739,Human_RBP_ID_25636444 RMVar_hsa_circ_25070,RMVar_hsa_circ_307880,RMVar_hsa_circ_359427,RMVar_hsa_circ_372592,RMVar_hsa_circ_308655,RMVar_hsa_circ_286862,RMVar_hsa_circ_65140,RMVar_hsa_circ_58772,RMVar_hsa_circ_124608,RMVar_hsa_circ_211725,RMVar_hsa_circ_211727,RMVar_hsa_circ_211728,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_66377,RMVar_hsa_circ_329754,RMVar_hsa_circ_211735,RMVar_hsa_circ_14147,RMVar_hsa_circ_211734 54714 RMVar_ID_54714 Human_SNP_ID_843657162 A-to-I Human chr21 - 31463055 31463055 31463055 TCCCCAGCCCTGGTGTGCTGCTAGACATAAGAAGAGGCAGGCTGGCTGGGCGCGGTGGCTCATGC TCCCCAGCCCTGGTGTGCTGCTAGACATAAGAGGAGGCAGGCTGGCTGGGCGCGGTGGCTCATGC T C TIAM1 Ensembl:ENSG00000156299 Protein coding intron GSE107867 ASD brains,cerebellum chr21:31463054..31463055 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 3 prostate Human_RBP_ID_14233242 RMVar_hsa_circ_368860,RMVar_hsa_circ_341353 54715 RMVar_ID_54715 Human_SNP_ID_843705404 A-to-I Human chr21 + 29028395 29028395 29028395 GTGATCCGCCTGCCTTGGCCTCCAAAAGTGCTAGGATTACACGTGAGAGCCACTGCACCTGACTT GTGATCCGCCTGCCTTGGCCTCCAAAAGTGCTGGGATTACACGTGAGAGCCACTGCACCTGACTT A G USP16 Ensembl:ENSG00000156256 Protein coding intron GSE100210 HepG2 cell line chr21:29028394..29028395 29129909 RNA-Seq:(High) rs1368993408 Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 4 pancreas Human_RBP_ID_14222456 RMVar_hsa_circ_12482,RMVar_hsa_circ_312965,RMVar_hsa_circ_353590,RMVar_hsa_circ_361454,RMVar_hsa_circ_362700,RMVar_hsa_circ_363615,RMVar_hsa_circ_354831,RMVar_hsa_circ_335105,RMVar_hsa_circ_68386,RMVar_hsa_circ_70161,RMVar_hsa_circ_211650,RMVar_hsa_circ_9814 54716 RMVar_ID_54716 Human_SNP_ID_843789993 A-to-I Human chr21 - 36885353 36885353 36885353 CAGGCGTGAGCCACCATGCCTGGATAATTTTTAAATTTTTTGTAGAGACAGGGGTCCCACTATGT CAGGCGTGAGCCACCATGCCTGGATAATTTTTTAATTTTTTGTAGAGACAGGGGTCCCACTATGT T A HLCS Ensembl:ENSG00000159267 Protein coding intron GSE100210 HepG2 cell line chr21:36885352..36885353 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 4 prostate Human_RBP_ID_14283538 RMVar_hsa_circ_38828,RMVar_hsa_circ_39806 54717 RMVar_ID_54717 Human_SNP_ID_843842712 A-to-I Human chr21 - 36962730 36962730 36962730 GGAGTGCAGTGGCATGATCTCATCTCACTGCAACCTCGGGCTCCCAGGCTCGAGTGATCCTCCCA GGAGTGCAGTGGCATGATCTCATCTCACTGCAGCCTCGGGCTCCCAGGCTCGAGTGATCCTCCCA T C HLCS Ensembl:ENSG00000159267 Protein coding intron GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line chr21:36962729..36962730 31158229 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 4 prostate 54718 RMVar_ID_54718 Human_SNP_ID_843884861 A-to-I Human chr21 + 33550950 33550950 33550950 CAGCCTTCGGTGACTGGGGTGCCAGAGTTGCCAGGGCTGCCTTCGGCAACTAGGGCACTGGAGTT CAGCCTTCGGTGACTGGGGTGCCAGAGTTGCCGGGGCTGCCTTCGGCAACTAGGGCACTGGAGTT A G SON Ensembl:ENSG00000159140 Protein coding CDS GSE100210 HepG2 cell line chr21:33550949..33550950 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 5 haematopoietic and lymphoid tissue Human_RBP_ID_1027662,Human_RBP_ID_1603246,Human_RBP_ID_1935774,Human_RBP_ID_3661055,Human_RBP_ID_5472445,Human_RBP_ID_7040108,Human_RBP_ID_8541263,Human_RBP_ID_8858727,Human_RBP_ID_9298853,Human_RBP_ID_17701222,Human_RBP_ID_17978913,Human_RBP_ID_18463591,Human_RBP_ID_18779876,Human_RBP_ID_22082150,Human_RBP_ID_22262311,Human_RBP_ID_22453971,Human_RBP_ID_26762074,Human_RBP_ID_26788811,Human_RBP_ID_27489669 Human_miRNA_ID_2933179 RMVar_hsa_circ_78630,RMVar_hsa_circ_121649,RMVar_hsa_circ_211887,RMVar_hsa_circ_89632,RMVar_hsa_circ_211889,RMVar_hsa_circ_211890 54719 RMVar_ID_54719 Human_SNP_ID_843910730 A-to-I Human chr21 + 33432979 33432979 33432979 ACAATCTCTGCTCACTGCAGCCTCCATCTCCCAGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTG ACAATCTCTGCTCACTGCAGCCTCCATCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCTG A G IFNGR2 Ensembl:ENSG00000159128 Protein coding intron GSE100210 HepG2 cell line chr21:33432978..33432979 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 RECA 1 - RMVar_hsa_circ_114090,RMVar_hsa_circ_85090,RMVar_hsa_circ_211858,RMVar_hsa_circ_115295,RMVar_hsa_circ_211865,RMVar_hsa_circ_211867,RMVar_hsa_circ_125196,RMVar_hsa_circ_211871 54720 RMVar_ID_54720 Human_SNP_ID_843963974 A-to-I Human chr21 - 10325728 10325728 10325728 CTGGCCAATACAGTGAAGCCCTGTCTCTACTAAAACTACAAAAAATTAGCCAGGCGTGGTGGCAG CTGGCCAATACAGTGAAGCCCTGTCTCTACTATAACTACAAAAAATTAGCCAGGCGTGGTGGCAG T A - - Other Unknown GSE100210 HepG2 cell line chr21:10325727..10325728 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 54721 RMVar_ID_54721 Human_SNP_ID_841186002 A-to-I Human chr20 - 49038561 49038561 49038561 CACCAAGTTGCTGATGAGTCTCTAGAAAGTACAAGGAGAATCCTGGGTTTAGCCATTGAGTCTCA CACCAAGTTGCTGATGAGTCTCTAGAAAGTACGAGGAGAATCCTGGGTTTAGCCATTGAGTCTCA T C SNAP23P1 Ensembl:ENSG00000230758 Pseudogene exon GSE100210 HepG2 cell line chr20:49038560..49038561 29129909 RNA-Seq:(High) rs1221502053 Functional Loss SNV ICGC 33..33 33 LAML 1 - 54722 RMVar_ID_54722 Human_SNP_ID_841207027 A-to-I Human chr20 - 4872883 4872883 4872883 AGGCCTGATGACGGGTGTCTGTAATTCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGGA AGGCCTGATGACGGGTGTCTGTAATTCCAGCTCCTCGGGAGGCTGAGGCAGGAGAATCGCTTGGA T G SLC23A2 Ensembl:ENSG00000089057 Protein coding intron GSE100210 HepG2 cell line chr20:4872882..4872883 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - RMVar_hsa_circ_77768,RMVar_hsa_circ_123079,RMVar_hsa_circ_60546,RMVar_hsa_circ_208555,RMVar_hsa_circ_208557,RMVar_hsa_circ_62159,RMVar_hsa_circ_208558,RMVar_hsa_circ_269529,RMVar_hsa_circ_350212 54723 RMVar_ID_54723 Human_SNP_ID_841227471 A-to-I Human chr20 - 23392463 23392463 23392463 TGAGGTCTTTTCATGTTGCCCAGGCTGGTCTCAAACTCCTGGACTCAAGCAGTCCTCCCATCTTG TGAGGTCTTTTCATGTTGCCCAGGCTGGTCTCTAACTCCTGGACTCAAGCAGTCCTCCCATCTTG T A NAPB Ensembl:ENSG00000125814 Protein coding intron GSE100210 HepG2 cell line chr20:23392462..23392463 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - RMVar_hsa_circ_5922,RMVar_hsa_circ_98404,RMVar_hsa_circ_73205,RMVar_hsa_circ_209075,RMVar_hsa_circ_363538,RMVar_hsa_circ_66601,RMVar_hsa_circ_321837,RMVar_hsa_circ_209076,RMVar_hsa_circ_96608,RMVar_hsa_circ_283391,RMVar_hsa_circ_347549,RMVar_hsa_circ_209077,RMVar_hsa_circ_60846 54724 RMVar_ID_54724 Human_SNP_ID_841242887 A-to-I Human chr20 + 5130823 5130823 5130823 AGAAAAGAAAAGCTCTGGAGGCTGGGCGTGGTAGCTCACGCCTGTAATCCCAGCACTTTGGGAGG AGAAAAGAAAAGCTCTGGAGGCTGGGCGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGG A G CDS2 Ensembl:ENSG00000101290 Protein coding intron GSE100210 HepG2 cell line chr20:5130822..5130823 29129909 RNA-Seq:(High) rs556987055 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue 54725 RMVar_ID_54725 Human_SNP_ID_841249484 A-to-I Human chr20 - 4899708 4899708 4899708 TCTCCTCTGACCCTTTTCCTGCCCACAGCACTACCTGACATGCTTCAGCGGCACGATCGCAGTGC TCTCCTCTGACCCTTTTCCTGCCCACAGCACTGCCTGACATGCTTCAGCGGCACGATCGCAGTGC T C SLC23A2 Ensembl:ENSG00000089057 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector chr20:4899707..4899708 29967493 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_19003763,Human_RBP_ID_25627522 Human_Splice_Rec_2057758,Human_Splice_Rec_2057790,Human_Splice_Rec_2057836 RMVar_hsa_circ_123079,RMVar_hsa_circ_208555,RMVar_hsa_circ_125920,RMVar_hsa_circ_62159,RMVar_hsa_circ_350212,RMVar_hsa_circ_124520,RMVar_hsa_circ_23379,RMVar_hsa_circ_28993,RMVar_hsa_circ_208560,RMVar_hsa_circ_208561,RMVar_hsa_circ_272244,RMVar_hsa_circ_208567,RMVar_hsa_circ_45104,RMVar_hsa_circ_208564,RMVar_hsa_circ_304025,RMVar_hsa_circ_306967,RMVar_hsa_circ_282954,RMVar_hsa_circ_208565,RMVar_hsa_circ_208566 54726 RMVar_ID_54726 Human_SNP_ID_841259488 A-to-I Human chr20 + 1336259 1336259 1336259 ATTAATCTAGGTGAGTATGCCATTTTGGAGATAGACAAACTGAGCCCTGGAGAGGTCAAATGACT ATTAATCTAGGTGAGTATGCCATTTTGGAGATGGACAAACTGAGCCCTGGAGAGGTCAAATGACT A G SDCBP2-AS1 Ensembl:ENSG00000234684 lincRNA intron GSE100210 HepG2 cell line chr20:1336258..1336259 29129909 RNA-Seq:(High) rs768658040 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_5249625 54727 RMVar_ID_54727 Human_SNP_ID_841280629 A-to-I Human chr20 + 36545234 36545234 36545234 CAACAGGGAAACTGGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAG CAACAGGGAAACTGGGCCGGGCGCGGTGGCTCGCGCCTGTAATCCCAGCACTTTGGGAGGCCAAG A G MYL9 Ensembl:ENSG00000101335 Protein coding intron GSE47997 K562 cells&HepG2 cells chr20:36545233..36545234 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 3 breast RMVar_hsa_circ_78663,RMVar_hsa_circ_113653,RMVar_hsa_circ_209859,RMVar_hsa_circ_209860 54728 RMVar_ID_54728 Human_SNP_ID_841286036 A-to-I Human chr20 - 17960594 17960594 17960594 TTGTGTGTGTTTTTTTGTTTGTTTGTTTTTTTAAGACGGAGTTTCGCTCTCATCGCCCAGGCTGG TTGTGTGTGTTTTTTTGTTTGTTTGTTTTTTTTAGACGGAGTTTCGCTCTCATCGCCCAGGCTGG T A SNX5,OVOL2 Ensembl:ENSG00000089006,Ensembl:ENSG00000125850 Protein coding,Protein coding intron,intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr20:17960593..17960594 24183664,29129909 RNA-Seq:(High) rs1568596270 Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_2678221,Human_RBP_ID_3643750,Human_RBP_ID_6981751,Human_RBP_ID_14042932 RMVar_hsa_circ_4170,RMVar_hsa_circ_318512,RMVar_hsa_circ_277337 54729 RMVar_ID_54729 Human_SNP_ID_841355707 A-to-I Human chr20 + 33640432 33640432 33640432 GAGGCAGAGCAGAAAGCCTTTGAAGTGATTGCAACAGAGAGAGCACGAATGGAGCAAACCATAGC GAGGCAGAGCAGAAAGCCTTTGAAGTGATTGCTACAGAGAGAGCACGAATGGAGCAAACCATAGC A T CBFA2T2 Ensembl:ENSG00000078699 Protein coding CDS GSE47997 K562 cells&HepG2 cells chr20:33640432..33640433 23474544 RNA-Seq:(High) - Functional Loss SNV TCGA 33..33 33 OV 1 - Human_RBP_ID_61960,Human_RBP_ID_8235083 Human_Splice_Rec_2073014,Human_Splice_Rec_2073015,Human_Splice_Rec_2073036,Human_Splice_Rec_2073037,Human_Splice_Rec_2073068,Human_Splice_Rec_2073069,Human_Splice_Rec_2073088,Human_Splice_Rec_2073089,Human_Splice_Rec_2073112,Human_Splice_Rec_2073113,Human_Splice_Rec_2073132,Human_Splice_Rec_2073133,Human_Splice_Rec_2073148,Human_Splice_Rec_2073149 RMVar_hsa_circ_268254,RMVar_hsa_circ_26567,RMVar_hsa_circ_9964,RMVar_hsa_circ_209417,RMVar_hsa_circ_289023,RMVar_hsa_circ_61315,RMVar_hsa_circ_341943,RMVar_hsa_circ_209423,RMVar_hsa_circ_209426,RMVar_hsa_circ_304838,RMVar_hsa_circ_347689 54730 RMVar_ID_54730 Human_SNP_ID_841362322 A-to-I Human chr20 + 41100086 41100086 41100086 AGAAAATCAAAGAGGAGAATGAAAAATTACTGAAAGAATATGGATTCTGTATTATGGATAACCAC AGAAAATCAAAGAGGAGAATGAAAAATTACTGGAAGAATATGGATTCTGTATTATGGATAACCAC A G TOP1 Ensembl:ENSG00000198900 Protein coding CDS GSE47997 K562 cells&HepG2 cells chr20:41100085..41100086 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 THCA 1 - Human_RBP_ID_63279,Human_RBP_ID_1929874,Human_RBP_ID_2695391,Human_RBP_ID_14109250,Human_RBP_ID_17511622,Human_RBP_ID_23905437,Human_RBP_ID_27021192 Human_Splice_Rec_2083692 RMVar_hsa_circ_9005,RMVar_hsa_circ_353056,RMVar_hsa_circ_210160,RMVar_hsa_circ_78804,RMVar_hsa_circ_210163,RMVar_hsa_circ_22116,RMVar_hsa_circ_327712,RMVar_hsa_circ_352483,RMVar_hsa_circ_377431,RMVar_hsa_circ_290728,RMVar_hsa_circ_291682,RMVar_hsa_circ_210165,RMVar_hsa_circ_48697,RMVar_hsa_circ_318564,RMVar_hsa_circ_13744,RMVar_hsa_circ_210166,RMVar_hsa_circ_210167 54731 RMVar_ID_54731 Human_SNP_ID_841379222 A-to-I Human chr20 - 44628279 44628279 44628279 CTCAGGTGATCTGCCCGCCTCGGCCTCCCAAAATGCTGGGATTACAGGCGTGAGCCACTGCGCCT CTCAGGTGATCTGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCGCCT T C ADA Ensembl:ENSG00000196839 Protein coding intron GSE38233 cultured B-cells chr20:44628278..44628279 24183664 RNA-Seq:(High) rs1202296397 Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 2 prostate 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 54732 RMVar_ID_54732 Human_SNP_ID_841407858 A-to-I Human chr20 - 34274725 34274725 34274725 CCAGGCTGGTCTCAAACTCCTGGGCTCAAGCAATCCTCCTGCCTCGGCCTCCCAAAGTGCTGGAA CCAGGCTGGTCTCAAACTCCTGGGCTCAAGCAGTCCTCCTGCCTCGGCCTCCCAAAGTGCTGGAA T C AL035458.2 Ensembl:ENSG00000250917 lincRNA intron GSE126723:GSM3611833,GSM3611834,GSM3611835 Bronchiolar epithelium,BERP35T4 cell line chr20:34274724..34274725 31158229 RNA-Seq:(High) rs761924730 Functional Loss SNV ICGC 33..33 33 MALY 1 - 54733 RMVar_ID_54733 Human_SNP_ID_841416780 A-to-I Human chr20 + 38983179 38983179 38983179 GACGTCAAGTGATCTGCCTACCTCAGCCTCCCAAAGTGCTGGGATTACCGGCATGAGCCGCCGTG GACGTCAAGTGATCTGCCTACCTCAGCCTCCCGAAGTGCTGGGATTACCGGCATGAGCCGCCGTG A G DHX35 Ensembl:ENSG00000101452 Protein coding intron GSE47997 K562 cells&HepG2 cells chr20:38983178..38983179 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_101465,RMVar_hsa_circ_49605,RMVar_hsa_circ_210141,RMVar_hsa_circ_322963,RMVar_hsa_circ_335983,RMVar_hsa_circ_301229,RMVar_hsa_circ_210143 54734 RMVar_ID_54734 Human_SNP_ID_841430478 A-to-I Human chr20 - 35281570 35281570 35281570 GTGGTGGCACGCACTTGTAATTCCAGCTACTCAGGAGGCCGAAGCAGGAGAATCACCTGAACCCA GTGGTGGCACGCACTTGTAATTCCAGCTACTCCGGAGGCCGAAGCAGGAGAATCACCTGAACCCA T G EIF6 Ensembl:ENSG00000242372 Protein coding intron GSE38233 cultured B-cells chr20:35281569..35281570 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 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 54735 RMVar_ID_54735 Human_SNP_ID_841451799 A-to-I Human chr20 - 63793714 63793714 63793714 ATGTGAACCGTTGTGAGGTAGCCGCTGCTTCTATAAAATCTTACGTGGAGGTGTGGACCGTTGTG ATGTGAACCGTTGTGAGGTAGCCGCTGCTTCTGTAAAATCTTACGTGGAGGTGTGGACCGTTGTG T C ZBTB46 Ensembl:ENSG00000130584 Protein coding intron GSE100210 HepG2 cell line chr20:63793713..63793714 29129909 RNA-Seq:(High) rs6062532 Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_17143372 54736 RMVar_ID_54736 Human_SNP_ID_841455097 A-to-I Human chr20 + 63899982 63899982 63899982 ACGGTTTCCGCTCATGGCAACCTCTGCCTCCTAGGTTCAAGTGATTCTCCTGCCTCAGCCTCCTG ACGGTTTCCGCTCATGGCAACCTCTGCCTCCTGGGTTCAAGTGATTCTCCTGCCTCAGCCTCCTG A G DNAJC5 Ensembl:ENSG00000101152 Protein coding intron GSE38233 cultured B-cells chr20:63899981..63899982 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_14169393 54737 RMVar_ID_54737 Human_SNP_ID_841493070 A-to-I Human chr20 + 36546639 36546639 36546639 CTCCAGGGTTCTTTTTTTTTCCCCCCGAGACAAAATCTCACTCTGTTGCCCAGGCTGGAGTGGCA CTCCAGGGTTCTTTTTTTTTCCCCCCGAGACATAATCTCACTCTGTTGCCCAGGCTGGAGTGGCA A T MYL9 Ensembl:ENSG00000101335 Protein coding intron GSE100210 HepG2 cell line chr20:36546639..36546640 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - RMVar_hsa_circ_78663,RMVar_hsa_circ_113653,RMVar_hsa_circ_209859,RMVar_hsa_circ_209860 54738 RMVar_ID_54738 Human_SNP_ID_841503509 A-to-I Human chr20 + 63714660 63714660 63714660 TTTTATCATGAAAGGGTGTTGATTTTTTTTTTAAAGATAGGGTCTTGTTCTGTCACCCAGGCTGG TTTTATCATGAAAGGGTGTTGATTTTTTTTTTTAAGATAGGGTCTTGTTCTGTCACCCAGGCTGG A T AL121845.3,ZGPAT Ensembl:ENSG00000273154,Ensembl:ENSG00000197114 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line chr20:63714660..63714661 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 pancreas ductal_carcinoma 5 pancreas 54739 RMVar_ID_54739 Human_SNP_ID_841515674 A-to-I Human chr20 - 51726845 51726845 51726845 TCTGGACGCAGTGGCTTAGGTCTGTAATCCCAACACTTTGGGAGGCTGAAGTGGGAGGATCGCTT TCTGGACGCAGTGGCTTAGGTCTGTAATCCCAGCACTTTGGGAGGCTGAAGTGGGAGGATCGCTT T C ATP9A Ensembl:ENSG00000054793 Protein coding intron GSE100210 HepG2 cell line chr20:51726844..51726845 29129909 RNA-Seq:(High) rs980751626 Functional Loss SNV ICGC 33..33 33 PRAD 1 - 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 54740 RMVar_ID_54740 Human_SNP_ID_841519464 A-to-I Human chr20 + 34448246 34448246 34448246 AAACCCGGTCTCTACTAAAAATACAAAAAGTTAGCTGGGCGTGGTGGCGCGTGCCTGTGATCCCA AAACCCGGTCTCTACTAAAAATACAAAAAGTTTGCTGGGCGTGGTGGCGCGTGCCTGTGATCCCA A T ITCH Ensembl:ENSG00000078747 Protein coding intron GSE100210 HepG2 cell line chr20:34448245..34448246 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_70065,RMVar_hsa_circ_42653,RMVar_hsa_circ_68688,RMVar_hsa_circ_73725,RMVar_hsa_circ_54559,RMVar_hsa_circ_2423,RMVar_hsa_circ_5653,RMVar_hsa_circ_20385,RMVar_hsa_circ_15901,RMVar_hsa_circ_74558,RMVar_hsa_circ_17294,RMVar_hsa_circ_345132,RMVar_hsa_circ_332425,RMVar_hsa_circ_342814,RMVar_hsa_circ_331034,RMVar_hsa_circ_298207,RMVar_hsa_circ_312079,RMVar_hsa_circ_317530,RMVar_hsa_circ_282182,RMVar_hsa_circ_46172,RMVar_hsa_circ_353253,RMVar_hsa_circ_358220,RMVar_hsa_circ_358804,RMVar_hsa_circ_329348,RMVar_hsa_circ_74987,RMVar_hsa_circ_19776,RMVar_hsa_circ_356201,RMVar_hsa_circ_369077,RMVar_hsa_circ_1408,RMVar_hsa_circ_372415,RMVar_hsa_circ_340478,RMVar_hsa_circ_354448,RMVar_hsa_circ_65757,RMVar_hsa_circ_71827,RMVar_hsa_circ_56972,RMVar_hsa_circ_77839,RMVar_hsa_circ_324046,RMVar_hsa_circ_354989,RMVar_hsa_circ_209515,RMVar_hsa_circ_209516,RMVar_hsa_circ_209517,RMVar_hsa_circ_364296,RMVar_hsa_circ_326127,RMVar_hsa_circ_302369,RMVar_hsa_circ_308316,RMVar_hsa_circ_209520,RMVar_hsa_circ_209522,RMVar_hsa_circ_209523,RMVar_hsa_circ_209521,RMVar_hsa_circ_336344,RMVar_hsa_circ_209518,RMVar_hsa_circ_209519,RMVar_hsa_circ_352832,RMVar_hsa_circ_326708,RMVar_hsa_circ_329558,RMVar_hsa_circ_67127,RMVar_hsa_circ_123584,RMVar_hsa_circ_209527,RMVar_hsa_circ_209528,RMVar_hsa_circ_209529,RMVar_hsa_circ_74368,RMVar_hsa_circ_209530 54741 RMVar_ID_54741 Human_SNP_ID_841538028 A-to-I Human chr20 + 36583999 36583999 36583999 TGAGGCAAGAGAATTGCTTGAACTCGGGAGGCAGAGGTTGTAGTGAGTTGTGATTGCACCATTGC TGAGGCAAGAGAATTGCTTGAACTCGGGAGGCGGAGGTTGTAGTGAGTTGTGATTGCACCATTGC A G TGIF2,TGIF2-RAB5IF Ensembl:ENSG00000118707,Ensembl:ENSG00000259399 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells chr20:36583998..36583999 24183664 RNA-Seq:(High) rs529476 Functional Loss SNV ICGC 33..33 33 LAML 1 - RMVar_hsa_circ_106038,RMVar_hsa_circ_117136,RMVar_hsa_circ_209863,RMVar_hsa_circ_87911,RMVar_hsa_circ_209865,RMVar_hsa_circ_209866 54742 RMVar_ID_54742 Human_SNP_ID_841556153 A-to-I Human chr20 + 34476127 34476127 34476127 AACTTCTCATATATGTGATCTTCAAAGATGAGATGACAGGTTAAACAAGCCAGAGTTCCCTCACA AACTTCTCATATATGTGATCTTCAAAGATGAGGTGACAGGTTAAACAAGCCAGAGTTCCCTCACA A G ITCH Ensembl:ENSG00000078747 Protein coding intron GSE100210 HepG2 cell line chr20:34476126..34476127 29129909 RNA-Seq:(High) rs545186305 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue RMVar_hsa_circ_73725,RMVar_hsa_circ_65265,RMVar_hsa_circ_20385,RMVar_hsa_circ_342814,RMVar_hsa_circ_312079,RMVar_hsa_circ_317530,RMVar_hsa_circ_46172,RMVar_hsa_circ_358220,RMVar_hsa_circ_19776,RMVar_hsa_circ_369077,RMVar_hsa_circ_340478,RMVar_hsa_circ_65757,RMVar_hsa_circ_56972,RMVar_hsa_circ_77839,RMVar_hsa_circ_209517,RMVar_hsa_circ_364296,RMVar_hsa_circ_209518,RMVar_hsa_circ_209519,RMVar_hsa_circ_123584,RMVar_hsa_circ_209529,RMVar_hsa_circ_209530,RMVar_hsa_circ_311040,RMVar_hsa_circ_362334,RMVar_hsa_circ_285039,RMVar_hsa_circ_75133,RMVar_hsa_circ_209543,RMVar_hsa_circ_209537,RMVar_hsa_circ_103259,RMVar_hsa_circ_209532,RMVar_hsa_circ_209533,RMVar_hsa_circ_209531,RMVar_hsa_circ_39183,RMVar_hsa_circ_8856,RMVar_hsa_circ_25229,RMVar_hsa_circ_274201,RMVar_hsa_circ_359105,RMVar_hsa_circ_300819,RMVar_hsa_circ_285273,RMVar_hsa_circ_271855,RMVar_hsa_circ_277290,RMVar_hsa_circ_209540,RMVar_hsa_circ_209541,RMVar_hsa_circ_209539,RMVar_hsa_circ_329670,RMVar_hsa_circ_333474,RMVar_hsa_circ_315352,RMVar_hsa_circ_209545,RMVar_hsa_circ_66296,RMVar_hsa_circ_209544,RMVar_hsa_circ_209542 54743 RMVar_ID_54743 Human_SNP_ID_841606053 A-to-I Human chr20 - 31285787 31285787 31285787 TGCTCTGACACTTCTTGAATACACTGAGACCCAGAATCAGTTCCTTGATGAGCTCATGGAACTTG TGCTCTGACACTTCTTGAATACACTGAGACCCGGAATCAGTTCCTTGATGAGCTCATGGAACTTG T C AL121723.1 Ensembl:ENSG00000224628 Pseudogene exon GSE100210 HepG2 cell line chr20:31285786..31285787 29129909 RNA-Seq:(High) rs879252735 Functional Loss SNV ICGC 33..33 33 LAML 2 - 54744 RMVar_ID_54744 Human_SNP_ID_841618129 A-to-I Human chr20 + 41038823 41038822 41038823 GCCTGGGCAACATGGGAAAAACCTGTCTCAACAAAAAAAATACAAAAATTAGCCAGGTGTGTTGG GCCTGGGCAACATGGGAAAAACCTGTCTCAAC_AAAAAAATACAAAAATTAGCCAGGTGTGTTGG CA C TOP1 Ensembl:ENSG00000198900 Protein coding intron GSE47997 K562 cells&HepG2 cells chr20:41038822..41038823;chr20:41038823..41038824 23474544 RNA-Seq:(High) - Functional Loss DEL ICGC 33..33 33 ESCA 1 - 54745 RMVar_ID_54745 Human_SNP_ID_841624534 A-to-I Human chr20 + 3891167 3891155 3891168 AACCTCCTGGGCTCAAGCCATCCTCCTGCTTCAACCTCCTGCATTGCTGGGACTAAAGGCACGTG AACCTCCTGGGCTCAAGCCAT_____________CCTCCTGCATTGCTGGGACTAAAGGCACGTG TCCTCCTGCTTCAA T PANK2 Ensembl:ENSG00000125779 Protein coding intron GSE100210 HepG2 cell line chr20:3891167..3891168 29129909 RNA-Seq:(High) rs935159481 Functional Loss DEL ICGC 22..34 33 ESCA 1 - RMVar_hsa_circ_85386,RMVar_hsa_circ_208515 54746 RMVar_ID_54746 Human_SNP_ID_841673687 A-to-I Human chr20 - 491619 491619 491619 TTGCCCAGGCTGGAGTGCAATGCCATGATCATAGCTGACTGCAGCCCCGAACTTCTGGGCTCAAG TTGCCCAGGCTGGAGTGCAATGCCATGATCATTGCTGACTGCAGCCCCGAACTTCTGGGCTCAAG T A CSNK2A1 Ensembl:ENSG00000101266 Protein coding intron GSE38233 cultured B-cells chr20:491618..491619 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_14124860 RMVar_hsa_circ_29190,RMVar_hsa_circ_118003,RMVar_hsa_circ_105940,RMVar_hsa_circ_208262,RMVar_hsa_circ_78590,RMVar_hsa_circ_82604,RMVar_hsa_circ_208264,RMVar_hsa_circ_208265,RMVar_hsa_circ_208263,RMVar_hsa_circ_208268,RMVar_hsa_circ_310206,RMVar_hsa_circ_345796,RMVar_hsa_circ_4492,RMVar_hsa_circ_208267,RMVar_hsa_circ_121316,RMVar_hsa_circ_208270 54747 RMVar_ID_54747 Human_SNP_ID_841681637 A-to-I Human chr20 - 37079605 37079605 37079605 AATGTTAGTGAAGTGTGGTGATATGCACCTGTAGTCCCAGCTATCTTGGGAGGCTGAGGTAGAGG AATGTTAGTGAAGTGTGGTGATATGCACCTGTGGTCCCAGCTATCTTGGGAGGCTGAGGTAGAGG T C RBL1 Ensembl:ENSG00000080839 Protein coding intron GSE38233 cultured B-cells chr20:37079604..37079605 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_41974,RMVar_hsa_circ_371616,RMVar_hsa_circ_209949,RMVar_hsa_circ_209954,RMVar_hsa_circ_75016 54748 RMVar_ID_54748 Human_SNP_ID_841691284 A-to-I Human chr20 - 49132707 49132684 49132707 TTGCGCAGGCTGGAGTACAATGGCACGATCTCAGCTTATGGCAACCTCCACCTCCTGGCTTCAAG TTGCGCAGGCTGGAGTACAATGGCACGATCTC_______________________TGGCTTCAAG AGGAGGTGGAGGTTGCCATAAGCT A STAU1 Ensembl:ENSG00000124214 Protein coding intron GSE100210 HepG2 cell line chr20:49132706..49132707 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 33..55 33 SKCA 1 - Human_RBP_ID_14128921 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_303409,RMVar_hsa_circ_321909,RMVar_hsa_circ_123744,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_81836,RMVar_hsa_circ_210733,RMVar_hsa_circ_65816,RMVar_hsa_circ_21386,RMVar_hsa_circ_365227,RMVar_hsa_circ_210734 54749 RMVar_ID_54749 Human_SNP_ID_841704480 A-to-I Human chr20 + 1336222 1336222 1336222 ATGAGAAAGAATCTCCCATGAGATCAGGGGCTAGCTCATTAATCTAGGTGAGTATGCCATTTTGG ATGAGAAAGAATCTCCCATGAGATCAGGGGCTGGCTCATTAATCTAGGTGAGTATGCCATTTTGG A G SDCBP2-AS1 Ensembl:ENSG00000234684 lincRNA intron GSE100210 HepG2 cell line chr20:1336221..1336222 29129909 RNA-Seq:(High) rs1385224691 Functional Loss SNV ICGC 33..33 33 LAML 1 - 54750 RMVar_ID_54750 Human_SNP_ID_841756738 A-to-I Human chr20 - 35630186 35630186 35630186 GGGTTCGAGCAATTCTTCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGTCGCTTGCCACCGTG GGGTTCGAGCAATTCTTCTGCCTCAGCCTCCCCAGTAGCTGGGACTACAGTCGCTTGCCACCGTG T G CPNE1 Ensembl:ENSG00000214078 Protein coding intron GSE38233;GSE123020:GSM3490832,GSM3490833,GSM3490834 cultured B-cells;esophageal squamous carcinoma cells,KYSE180 cell line chr20:35630185..35630186 24183664,32596459 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 4 ovary RMVar_hsa_circ_47999,RMVar_hsa_circ_116446,RMVar_hsa_circ_69220,RMVar_hsa_circ_21402,RMVar_hsa_circ_39545,RMVar_hsa_circ_209722 54751 RMVar_ID_54751 Human_SNP_ID_841777506 A-to-I Human chr20 - 35639451 35639451 35639451 GTGCCTGTAATCCCAGCTACTCTGGAGGCTGTAGTGGGAGAATCGCTGGAACCCAGGAGGCGGAG GTGCCTGTAATCCCAGCTACTCTGGAGGCTGTGGTGGGAGAATCGCTGGAACCCAGGAGGCGGAG T C AL109827.1,CPNE1 Ensembl:ENSG00000272897,Ensembl:ENSG00000214078 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line chr20:35639450..35639451 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_14085663,Human_RBP_ID_25629520 RMVar_hsa_circ_47999,RMVar_hsa_circ_371126,RMVar_hsa_circ_374552,RMVar_hsa_circ_336427,RMVar_hsa_circ_209726,RMVar_hsa_circ_209727 54752 RMVar_ID_54752 Human_SNP_ID_841783239 A-to-I Human chr20 - 30396951 30396951 30396951 CTGTAGGTCTAAAAGGAAAAGCATACATACACATAATTGATTTCACATTGTTTTACATTTCCTTT CTGTAGGTCTAAAAGGAAAAGCATACATACACGTAATTGATTTCACATTGTTTTACATTTCCTTT T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr20:30396950..30396951 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 COCA 1 - 54753 RMVar_ID_54753 Human_SNP_ID_841810515 A-to-I Human chr20 + 45884755 45884755 45884755 CAATCCAGCTGGGCATGGTGGCTCACGCCTGTAATCCCAGCATTTTGGGAGGCTGAGGTGGACAG CAATCCAGCTGGGCATGGTGGCTCACGCCTGTGATCCCAGCATTTTGGGAGGCTGAGGTGGACAG A G ZSWIM1 Ensembl:ENSG00000168612 Protein coding 3'UTR GSE100210 HepG2 cell line chr20:45884754..45884755;chr20:45884755..45884756 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA 33..33 33 ESCA 1 - RMVar_hsa_circ_119690,RMVar_hsa_circ_210406 54754 RMVar_ID_54754 Human_SNP_ID_841817819 A-to-I Human chr20 + 47540452 47540452 47540452 AAAATTAGCTGGGCATGGTGGTGGGTGCCTGTAATCCGGCTACTTGAGAGGCTGAGGAAGGAGAA AAAATTAGCTGGGCATGGTGGTGGGTGCCTGTCATCCGGCTACTTGAGAGGCTGAGGAAGGAGAA A C NCOA3 Ensembl:ENSG00000124151 Protein coding intron GSE38233 cultured B-cells chr20:47540452..47540453 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_21936488 RMVar_hsa_circ_210526,RMVar_hsa_circ_95052,RMVar_hsa_circ_210527 54755 RMVar_ID_54755 Human_SNP_ID_841819477 A-to-I Human chr20 - 47265526 47265526 47265526 TGAGGCAGGAGAATTGCTTGAACCTGGCAGGCAGAGGTTGCAGTGAGCTGAGATCACCCCACTGC TGAGGCAGGAGAATTGCTTGAACCTGGCAGGCGGAGGTTGCAGTGAGCTGAGATCACCCCACTGC T C ZMYND8 Ensembl:ENSG00000101040 Protein coding intron GSE38233 cultured B-cells chr20:47265525..47265526 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_210488,RMVar_hsa_circ_3666,RMVar_hsa_circ_73732,RMVar_hsa_circ_4641,RMVar_hsa_circ_117845,RMVar_hsa_circ_82182,RMVar_hsa_circ_210472,RMVar_hsa_circ_210473,RMVar_hsa_circ_300845,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_281763,RMVar_hsa_circ_62862,RMVar_hsa_circ_87810,RMVar_hsa_circ_210482,RMVar_hsa_circ_210484,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_270363,RMVar_hsa_circ_210492,RMVar_hsa_circ_77505,RMVar_hsa_circ_96252,RMVar_hsa_circ_210494,RMVar_hsa_circ_210495,RMVar_hsa_circ_210493,RMVar_hsa_circ_210490,RMVar_hsa_circ_210491,RMVar_hsa_circ_210489,RMVar_hsa_circ_210486,RMVar_hsa_circ_210487 54756 RMVar_ID_54756 Human_SNP_ID_841851689 A-to-I Human chr20 + 63724314 63724314 63724314 CTTGAACCTGGGAAGCGGAGGTTGCAGTGAGCAAGATCGCACCACTGCATTACAGCCTAGATGAC CTTGAACCTGGGAAGCGGAGGTTGCAGTGAGCGAGATCGCACCACTGCATTACAGCCTAGATGAC A G AL121845.3,ZGPAT Ensembl:ENSG00000273154,Ensembl:ENSG00000197114 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line chr20:63724314..63724315 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - 54757 RMVar_ID_54757 Human_SNP_ID_841890149 A-to-I Human chr20 + 34476148 34476148 34476148 TCAAAGATGAGATGACAGGTTAAACAAGCCAGAGTTCCCTCACATGCACCAAAGCCATCAATATC TCAAAGATGAGATGACAGGTTAAACAAGCCAGGGTTCCCTCACATGCACCAAAGCCATCAATATC A G ITCH Ensembl:ENSG00000078747 Protein coding intron GSE100210 HepG2 cell line chr20:34476147..34476148 29129909 RNA-Seq:(High) rs542643642 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue RMVar_hsa_circ_73725,RMVar_hsa_circ_65265,RMVar_hsa_circ_20385,RMVar_hsa_circ_342814,RMVar_hsa_circ_312079,RMVar_hsa_circ_317530,RMVar_hsa_circ_46172,RMVar_hsa_circ_358220,RMVar_hsa_circ_19776,RMVar_hsa_circ_369077,RMVar_hsa_circ_340478,RMVar_hsa_circ_65757,RMVar_hsa_circ_56972,RMVar_hsa_circ_77839,RMVar_hsa_circ_209517,RMVar_hsa_circ_364296,RMVar_hsa_circ_209518,RMVar_hsa_circ_209519,RMVar_hsa_circ_123584,RMVar_hsa_circ_209529,RMVar_hsa_circ_209530,RMVar_hsa_circ_311040,RMVar_hsa_circ_362334,RMVar_hsa_circ_285039,RMVar_hsa_circ_75133,RMVar_hsa_circ_209543,RMVar_hsa_circ_209537,RMVar_hsa_circ_103259,RMVar_hsa_circ_209532,RMVar_hsa_circ_209533,RMVar_hsa_circ_209531,RMVar_hsa_circ_39183,RMVar_hsa_circ_8856,RMVar_hsa_circ_25229,RMVar_hsa_circ_274201,RMVar_hsa_circ_359105,RMVar_hsa_circ_300819,RMVar_hsa_circ_285273,RMVar_hsa_circ_271855,RMVar_hsa_circ_277290,RMVar_hsa_circ_209540,RMVar_hsa_circ_209541,RMVar_hsa_circ_209539,RMVar_hsa_circ_329670,RMVar_hsa_circ_333474,RMVar_hsa_circ_315352,RMVar_hsa_circ_209545,RMVar_hsa_circ_66296,RMVar_hsa_circ_209544,RMVar_hsa_circ_209542 54758 RMVar_ID_54758 Human_SNP_ID_841906237 A-to-I Human chr20 + 49031299 49031299 49031299 TCGCCCAGGCTGGAGTGCAGTGGTGCAATCTCAGTTTACTGCAACCTCCACCTCCTGAGTTCAAG TCGCCCAGGCTGGAGTGCAGTGGTGCAATCTCCGTTTACTGCAACCTCCACCTCCTGAGTTCAAG A C ARFGEF2 Ensembl:ENSG00000124198 Protein coding intron GSE38233 cultured B-cells chr20:49031298..49031299 24183664 RNA-Seq:(High) rs923931167 Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_121409,RMVar_hsa_circ_210609,RMVar_hsa_circ_266014,RMVar_hsa_circ_99880,RMVar_hsa_circ_210637,RMVar_hsa_circ_5717,RMVar_hsa_circ_361816,RMVar_hsa_circ_282997 54759 RMVar_ID_54759 Human_SNP_ID_841931096 A-to-I Human chr20 + 5190372 5190372 5190372 TCTTTTTTTTTTTTTTTTGGAGGGTATTTTTTATTTGTGGGTTCAAAAAATCTGTATATACAGTC TCTTTTTTTTTTTTTTTTGGAGGGTATTTTTTTTTTGTGGGTTCAAAAAATCTGTATATACAGTC A T CDS2 Ensembl:ENSG00000101290 Protein coding 3'UTR GSE38233 cultured B-cells chr20:5190371..5190372 24183664 RNA-Seq:(High) rs879006229 Functional Loss SNV ICGC,COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,colon adenocarcinoma,LUSC,brain astrocytoma_Grade_IV,large_intestine adenocarcinoma 4 large intestine,brain Human_RBP_ID_566680,Human_RBP_ID_3651551,Human_RBP_ID_7013318,Human_RBP_ID_14143758,Human_RBP_ID_20668552,Human_RBP_ID_22395355,Human_RBP_ID_24424427,Human_RBP_ID_24492311,Human_RBP_ID_27703135 Human_miRNA_ID_855187 RMVar_hsa_circ_208596,RMVar_hsa_circ_119062,RMVar_hsa_circ_208598 54760 RMVar_ID_54760 Human_SNP_ID_841934113 A-to-I Human chr20 + 64009647 64009647 64009647 TTAGAGGCTGAGACAGGAGAATCTCTGAACCCAGGAAGCGGAGGTAGCAGTCAGCTGAGATCGTG TTAGAGGCTGAGACAGGAGAATCTCTGAACCCGGGAAGCGGAGGTAGCAGTCAGCTGAGATCGTG A G PRPF6 Ensembl:ENSG00000101161 Protein coding intron GSE100210 HepG2 cell line chr20:64009646..64009647 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_14171392 RMVar_hsa_circ_45960,RMVar_hsa_circ_123569,RMVar_hsa_circ_269558,RMVar_hsa_circ_211371,RMVar_hsa_circ_77707,RMVar_hsa_circ_120096,RMVar_hsa_circ_211372,RMVar_hsa_circ_211373,RMVar_hsa_circ_88388,RMVar_hsa_circ_351826,RMVar_hsa_circ_211377,RMVar_hsa_circ_211374,RMVar_hsa_circ_211375,RMVar_hsa_circ_79542,RMVar_hsa_circ_103155,RMVar_hsa_circ_211378 54761 RMVar_ID_54761 Human_SNP_ID_841940274 A-to-I Human chr20 - 36772295 36772295 36772295 GACAGAGTGAGATTCCACCTCAAAAAAAAACAAAAACAAAGAATAGACTGGAGACGGGCCGTTGG GACAGAGTGAGATTCCACCTCAAAAAAAAACAGAAACAAAGAATAGACTGGAGACGGGCCGTTGG T C DSN1 Ensembl:ENSG00000149636 Protein coding intron GSE126723:GSM3611827,GSM3611828,GSM3611829 Bronchiolar epithelium,BEP2D cell line chr20:36772294..36772295 31158229 RNA-Seq:(High) rs544574071 Functional Loss SNV ICGC 33..33 33 PBCA 1 - 54762 RMVar_ID_54762 Human_SNP_ID_841943234 A-to-I Human chr20 - 35677834 35677834 35677834 GAATTCCTGACCTCAAGCAACCCTCCCGCCTCAGTCTCCCAAAGTGCTGGGATTACAGGCATGAC GAATTCCTGACCTCAAGCAACCCTCCCGCCTCGGTCTCCCAAAGTGCTGGGATTACAGGCATGAC T C NFS1 Ensembl:ENSG00000244005 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr20:35677833..35677834 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_60187,RMVar_hsa_circ_352515 54763 RMVar_ID_54763 Human_SNP_ID_841978278 A-to-I Human chr20 + 34476137 34476137 34476137 ATATGTGATCTTCAAAGATGAGATGACAGGTTAAACAAGCCAGAGTTCCCTCACATGCACCAAAG ATATGTGATCTTCAAAGATGAGATGACAGGTTGAACAAGCCAGAGTTCCCTCACATGCACCAAAG A G ITCH Ensembl:ENSG00000078747 Protein coding intron GSE100210 HepG2 cell line chr20:34476136..34476137 29129909 RNA-Seq:(High) rs572085948 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue RMVar_hsa_circ_73725,RMVar_hsa_circ_65265,RMVar_hsa_circ_20385,RMVar_hsa_circ_342814,RMVar_hsa_circ_312079,RMVar_hsa_circ_317530,RMVar_hsa_circ_46172,RMVar_hsa_circ_358220,RMVar_hsa_circ_19776,RMVar_hsa_circ_369077,RMVar_hsa_circ_340478,RMVar_hsa_circ_65757,RMVar_hsa_circ_56972,RMVar_hsa_circ_77839,RMVar_hsa_circ_209517,RMVar_hsa_circ_364296,RMVar_hsa_circ_209518,RMVar_hsa_circ_209519,RMVar_hsa_circ_123584,RMVar_hsa_circ_209529,RMVar_hsa_circ_209530,RMVar_hsa_circ_311040,RMVar_hsa_circ_362334,RMVar_hsa_circ_285039,RMVar_hsa_circ_75133,RMVar_hsa_circ_209543,RMVar_hsa_circ_209537,RMVar_hsa_circ_103259,RMVar_hsa_circ_209532,RMVar_hsa_circ_209533,RMVar_hsa_circ_209531,RMVar_hsa_circ_39183,RMVar_hsa_circ_8856,RMVar_hsa_circ_25229,RMVar_hsa_circ_274201,RMVar_hsa_circ_359105,RMVar_hsa_circ_300819,RMVar_hsa_circ_285273,RMVar_hsa_circ_271855,RMVar_hsa_circ_277290,RMVar_hsa_circ_209540,RMVar_hsa_circ_209541,RMVar_hsa_circ_209539,RMVar_hsa_circ_329670,RMVar_hsa_circ_333474,RMVar_hsa_circ_315352,RMVar_hsa_circ_209545,RMVar_hsa_circ_66296,RMVar_hsa_circ_209544,RMVar_hsa_circ_209542 54764 RMVar_ID_54764 Human_SNP_ID_842010852 A-to-I Human chr20 + 11894808 11894808 11894808 GGAAAGCCCAGAAAGACCCTGCAAATGGCCCCAGTGAAAAACTCAGGAGAAGCAGTAAGCAGTCA GGAAAGCCCAGAAAGACCCTGCAAATGGCCCCGGTGAAAAACTCAGGAGAAGCAGTAAGCAGTCA A G BTBD3 Ensembl:ENSG00000132640 Protein coding intron GSE100210 HepG2 cell line chr20:11894807..11894808 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 5 prostate Human_RBP_ID_832292 RMVar_hsa_circ_109284,RMVar_hsa_circ_208733 54765 RMVar_ID_54765 Human_SNP_ID_842020422 A-to-I Human chr20 - 44311109 44311109 44311109 ATCTGGAGCGCTGCGAGTGGTTGTTGCGGGGGACGCTGGTGCGGGCGGCCGTGCGGCGCTACCTG ATCTGGAGCGCTGCGAGTGGTTGTTGCGGGGGGCGCTGGTGCGGGCGGCCGTGCGGCGCTACCTG T C FITM2 Ensembl:ENSG00000197296 Protein coding CDS GSE100210 HepG2 cell line chr20:44311109..44311110 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_4659410,Human_RBP_ID_5148430,Human_RBP_ID_22453100 54766 RMVar_ID_54766 Human_SNP_ID_842048307 A-to-I Human chr20 - 34863463 34863463 34863463 TCGGAGATGGGCAGCCAAGACGGGTCGCCGCTACGCGAGACGCGCAAAGACCCGTTCTCCGCCGC TCGGAGATGGGCAGCCAAGACGGGTCGCCGCTGCGCGAGACGCGCAAAGACCCGTTCTCCGCCGC T C GGT7 Ensembl:ENSG00000131067 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector chr20:34863462..34863463 29967493 RNA-Seq:(High) rs1479361034 Functional Loss SNV COSMIC 33..33 33 large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_4642992,Human_RBP_ID_9390389,Human_RBP_ID_22453036,Human_RBP_ID_23115448 Human_Splice_Rec_2074606,Human_Splice_Rec_2074650 Human_miRNA_ID_2158167 RMVar_hsa_circ_100195,RMVar_hsa_circ_209610 54767 RMVar_ID_54767 Human_SNP_ID_842138065 A-to-I Human chr20 - 34563311 34563311 34563311 CGCCTGCTTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCGCACCTCGCCGAAGTTT CGCCTGCTTCGGCCTCCCAAAGTGCTGGGATTGCAGGCATGAGCCACCGCACCTCGCCGAAGTTT T C PIGU Ensembl:ENSG00000101464 Protein coding intron GSE100210 HepG2 cell line chr20:34563310..34563311 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 2 breast RMVar_hsa_circ_78899,RMVar_hsa_circ_99339,RMVar_hsa_circ_107662,RMVar_hsa_circ_114865,RMVar_hsa_circ_104892,RMVar_hsa_circ_96280,RMVar_hsa_circ_209564,RMVar_hsa_circ_209566,RMVar_hsa_circ_209567,RMVar_hsa_circ_209568,RMVar_hsa_circ_209565,RMVar_hsa_circ_209569 54768 RMVar_ID_54768 Human_SNP_ID_842298658 A-to-I Human chr20 + 43653164 43653164 43653164 GCCTGGGGCTGCTCCCCTCATTGATGTGGTGCAATCGGGCTACTACAAAGTTCTGGGAAAGGAAA GCCTGGGGCTGCTCCCCTCATTGATGTGGTGCGATCGGGCTACTACAAAGTTCTGGGAAAGGAAA A G RPL27AP Ensembl:ENSG00000215467 Pseudogene exon GSE100210 HepG2 cell line chr20:43653163..43653164 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_564494,Human_RBP_ID_1026160,Human_RBP_ID_5445644,Human_RBP_ID_7003560,Human_RBP_ID_8854942,Human_RBP_ID_17667840 Human_miRNA_ID_1846701,Human_miRNA_ID_1855930,Human_miRNA_ID_1863907,Human_miRNA_ID_1864264,Human_miRNA_ID_1911647,Human_miRNA_ID_1911751 54769 RMVar_ID_54769 Human_SNP_ID_842376672 A-to-I Human chr20 + 41100075 41100074 41100075 TGCTGTCTTCCAGAAAATCAAAGAGGAGAATGAAAAATTACTGAAAGAATATGGATTCTGTATTA TGCTGTCTTCCAGAAAATCAAAGAGGAGAATG_AAAATTACTGAAAGAATATGGATTCTGTATTA GA G TOP1 Ensembl:ENSG00000198900 Protein coding CDS GSE47997 K562 cells&HepG2 cells chr20:41100074..41100075 23474544 RNA-Seq:(High) - Functional Loss DEL TCGA 33..33 33 COAD 1 - Human_RBP_ID_1929874,Human_RBP_ID_2695391,Human_RBP_ID_23002273,Human_RBP_ID_23905437,Human_RBP_ID_27701937 Human_Splice_Rec_2083692 RMVar_hsa_circ_9005,RMVar_hsa_circ_353056,RMVar_hsa_circ_210160,RMVar_hsa_circ_78804,RMVar_hsa_circ_210163,RMVar_hsa_circ_22116,RMVar_hsa_circ_327712,RMVar_hsa_circ_352483,RMVar_hsa_circ_377431,RMVar_hsa_circ_290728,RMVar_hsa_circ_291682,RMVar_hsa_circ_210165,RMVar_hsa_circ_48697,RMVar_hsa_circ_318564,RMVar_hsa_circ_13744,RMVar_hsa_circ_210166,RMVar_hsa_circ_210167 54770 RMVar_ID_54770 Human_SNP_ID_842387448 A-to-I Human chr20 + 31550062 31550062 31550062 TTCCCTTCATACTGCTCTTTTTTTCTCCTTCTAGGTATTTGGCACCAATGTGATGGTGACAGTGG TTCCCTTCATACTGCTCTTTTTTTCTCCTTCTTGGTATTTGGCACCAATGTGATGGTGACAGTGG A T HM13 Ensembl:ENSG00000101294 Protein coding intron GSE100210 HepG2 cell line chr20:31550061..31550062 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 breast ER-PR-positive_carcinoma 3 breast Human_RBP_ID_62435,Human_RBP_ID_2680123,Human_RBP_ID_3960088,Human_RBP_ID_22670746,Human_RBP_ID_22766944,Human_RBP_ID_22817046,Human_RBP_ID_25627677,Human_RBP_ID_27018782,Human_RBP_ID_27295123 Human_Splice_Rec_2069979,Human_Splice_Rec_2070003,Human_Splice_Rec_2070027,Human_Splice_Rec_2070051,Human_Splice_Rec_2070075,Human_Splice_Rec_2070101,Human_Splice_Rec_2070127,Human_Splice_Rec_2070157,Human_Splice_Rec_2070175,Human_Splice_Rec_2070193,Human_Splice_Rec_2070201,Human_Splice_Rec_2070219,Human_Splice_Rec_2070235,Human_Splice_Rec_2070251,Human_Splice_Rec_2070265,Human_Splice_Rec_2070287,Human_Splice_Rec_2070293,Human_Splice_Rec_2070303,Human_Splice_Rec_2070317,Human_Splice_Rec_2070333 RMVar_hsa_circ_209191,RMVar_hsa_circ_26002,RMVar_hsa_circ_209186,RMVar_hsa_circ_99051,RMVar_hsa_circ_90576,RMVar_hsa_circ_378630,RMVar_hsa_circ_209192,RMVar_hsa_circ_108729,RMVar_hsa_circ_22046,RMVar_hsa_circ_302780,RMVar_hsa_circ_269849,RMVar_hsa_circ_209193,RMVar_hsa_circ_209194,RMVar_hsa_circ_35749,RMVar_hsa_circ_369801,RMVar_hsa_circ_209195,RMVar_hsa_circ_209196,RMVar_hsa_circ_321194 54771 RMVar_ID_54771 Human_SNP_ID_842395213 A-to-I Human chr20 - 44661371 44661371 44661371 AAATTAGGTGGGCGTGGTGGCGGGCACCTGTAATCTCAGCTACTCGGGAGGCTGAGGCAGGAGAA AAATTAGGTGGGCGTGGTGGCGGGCACCTGTACTCTCAGCTACTCGGGAGGCTGAGGCAGGAGAA T G LINC01260,AL139352.1 Ensembl:ENSG00000283440,Ensembl:ENSG00000132832 lincRNA,lincRNA intron,intron GSE47997 K562 cells&HepG2 cells chr20:44661370..44661371 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 54772 RMVar_ID_54772 Human_SNP_ID_842402132 A-to-I Human chr20 + 3919072 3919072 3919072 GGGATTACAAGTGTGCGCCCCCACACCCTGCTAATTTTTGTACTTTCAGTAGAAATGGGGTTTCA GGGATTACAAGTGTGCGCCCCCACACCCTGCTCATTTTTGTACTTTCAGTAGAAATGGGGTTTCA A C PANK2 Ensembl:ENSG00000125779 Protein coding intron GSE100210 HepG2 cell line chr20:3919071..3919072 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 5 prostate Human_RBP_ID_17571355 54773 RMVar_ID_54773 Human_SNP_ID_842424072 A-to-I Human chr20 - 44500259 44500259 44500259 CTGAGTGCCAAGGACACCACTGGAACTCACAAAGGTCTCCTTCACCGAAAACCCATATACCTTTT CTGAGTGCCAAGGACACCACTGGAACTCACAAGGGTCTCCTTCACCGAAAACCCATATACCTTTT T C SERINC3 Ensembl:ENSG00000132824 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector chr20:44500258..44500259 29967493 RNA-Seq:(High) rs1057016339 Functional Loss SNV TCGA,ICGC 33..33 33 SARC 2 - Human_RBP_ID_927169,Human_RBP_ID_1597719,Human_RBP_ID_1930270,Human_RBP_ID_8534074,Human_RBP_ID_17281611,Human_RBP_ID_17395566,Human_RBP_ID_17511759,Human_RBP_ID_18773786,Human_RBP_ID_22395182,Human_RBP_ID_22452781,Human_RBP_ID_27486140 Human_Splice_Rec_2086775,Human_Splice_Rec_2086795 Human_miRNA_ID_2622064,Human_miRNA_ID_2622065,Human_miRNA_ID_3080111,Human_miRNA_ID_3080112 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 54774 RMVar_ID_54774 Human_SNP_ID_842440486 A-to-I Human chr20 - 5584128 5584128 5584128 TTTGGTCAAAGACAGGCCACACGTGCAGCAGCAGTCTCATATGATTATAATGAAGCTGAAAAATT TTTGGTCAAAGACAGGCCACACGTGCAGCAGCGGTCTCATATGATTATAATGAAGCTGAAAAATT T C GPCPD1 Ensembl:ENSG00000125772 Protein coding intron GSE38233 cultured B-cells chr20:5584127..5584128 24183664 RNA-Seq:(High) rs6053517 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 4 large intestine GWAS_ID_1988,GWAS_ID_1989,GWAS_ID_1990,GWAS_ID_1991,GWAS_ID_1992,GWAS_ID_1993,GWAS_ID_1994,GWAS_ID_1995,GWAS_ID_1996,GWAS_ID_1997,GWAS_ID_1998,GWAS_ID_1999,GWAS_ID_2000 RMVar_hsa_circ_5768,RMVar_hsa_circ_305105,RMVar_hsa_circ_330101,RMVar_hsa_circ_304782,RMVar_hsa_circ_46097,RMVar_hsa_circ_208603,RMVar_hsa_circ_208604,RMVar_hsa_circ_62086,RMVar_hsa_circ_337741,RMVar_hsa_circ_368063,RMVar_hsa_circ_317545,RMVar_hsa_circ_52985,RMVar_hsa_circ_208610,RMVar_hsa_circ_284624,RMVar_hsa_circ_2151,RMVar_hsa_circ_112779,RMVar_hsa_circ_3111,RMVar_hsa_circ_7694,RMVar_hsa_circ_343120,RMVar_hsa_circ_208612,RMVar_hsa_circ_305742,RMVar_hsa_circ_346212,RMVar_hsa_circ_25003 54775 RMVar_ID_54775 Human_SNP_ID_842450988 A-to-I Human chr20 - 25528108 25528108 25528108 AGAGGATCTCTTGAGCCCAAGAGTTCAAGGTTACAGTGAGCTATGATTGTGCCACTGCACTCCAG AGAGGATCTCTTGAGCCCAAGAGTTCAAGGTTGCAGTGAGCTATGATTGTGCCACTGCACTCCAG T C NINL Ensembl:ENSG00000101004 Protein coding intron GSE47997 K562 cells&HepG2 cells chr20:25528107..25528108 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 BRCA 1 - 54776 RMVar_ID_54776 Human_SNP_ID_842458673 A-to-I Human chr20 + 38529397 38529397 38529397 AAAATTAGCAGGGTGTGATGGCACATGCCTGTAGTCTCAGCTACTTGGGAGGCTGAGATAGGAGA AAAATTAGCAGGGTGTGATGGCACATGCCTGTTGTCTCAGCTACTTGGGAGGCTGAGATAGGAGA A T RALGAPB Ensembl:ENSG00000170471 Protein coding intron GSE100210 HepG2 cell line chr20:38529396..38529397 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_18447,RMVar_hsa_circ_210089,RMVar_hsa_circ_83005,RMVar_hsa_circ_324912,RMVar_hsa_circ_51847,RMVar_hsa_circ_109189,RMVar_hsa_circ_210095,RMVar_hsa_circ_368052,RMVar_hsa_circ_288642,RMVar_hsa_circ_328368,RMVar_hsa_circ_210101,RMVar_hsa_circ_210100,RMVar_hsa_circ_47095,RMVar_hsa_circ_210102,RMVar_hsa_circ_368643,RMVar_hsa_circ_84636,RMVar_hsa_circ_42623,RMVar_hsa_circ_210109,RMVar_hsa_circ_210106,RMVar_hsa_circ_303655,RMVar_hsa_circ_210103,RMVar_hsa_circ_323516,RMVar_hsa_circ_323775,RMVar_hsa_circ_36263,RMVar_hsa_circ_45054,RMVar_hsa_circ_210108,RMVar_hsa_circ_210107,RMVar_hsa_circ_1189,RMVar_hsa_circ_314892,RMVar_hsa_circ_210110 54777 RMVar_ID_54777 Human_SNP_ID_842465055 A-to-I Human chr20 - 35052783 35052783 35052783 TTCAAAAGTTTAAAAAGTACTGTTGGCCGGGCACGGTGGCTATCACCTGTAATCCCAGCAATTTG TTCAAAAGTTTAAAAAGTACTGTTGGCCGGGCTCGGTGGCTATCACCTGTAATCCCAGCAATTTG T A TRPC4AP Ensembl:ENSG00000100991 Protein coding intron GSE100210 HepG2 cell line chr20:35052782..35052783 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - 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 54778 RMVar_ID_54778 Human_SNP_ID_842469753 A-to-I Human chr20 + 63677468 63677468 63677468 GAAACCCCATCTCTACTAAAAATGCGAAAATTAGCCGGGCATGGTGGCGCACACCTATAGTCCCA GAAACCCCATCTCTACTAAAAATGCGAAAATTGGCCGGGCATGGTGGCGCACACCTATAGTCCCA A G RTEL1-TNFRSF6B,RTEL1 Ensembl:ENSG00000026036,Ensembl:ENSG00000258366 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line chr20:63677467..63677468 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_6246,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 54779 RMVar_ID_54779 Human_SNP_ID_842515136 A-to-I Human chr20 - 3295773 3295773 3295773 ACTGAATATTGAAGCTGCAGAACATCATTTGCAGGACAAGGAGGACTTCCAGAATAAAGTGGACA ACTGAATATTGAAGCTGCAGAACATCATTTGCGGGACAAGGAGGACTTCCAGAATAAAGTGGACA T C C20orf194 Ensembl:ENSG00000088854 Protein coding intron GSE100210 HepG2 cell line chr20:3295772..3295773 29129909 RNA-Seq:(High) rs879194491 Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_14075171 RMVar_hsa_circ_7379,RMVar_hsa_circ_10209,RMVar_hsa_circ_336893,RMVar_hsa_circ_8916,RMVar_hsa_circ_38395,RMVar_hsa_circ_280352,RMVar_hsa_circ_50634,RMVar_hsa_circ_12905,RMVar_hsa_circ_20089,RMVar_hsa_circ_347147,RMVar_hsa_circ_16214,RMVar_hsa_circ_286355,RMVar_hsa_circ_12726,RMVar_hsa_circ_346113,RMVar_hsa_circ_307886,RMVar_hsa_circ_10943,RMVar_hsa_circ_10873 54780 RMVar_ID_54780 Human_SNP_ID_842542754 A-to-I Human chr20 + 43672200 43672200 43672200 GCCACTTCACTCTAGCCTGGGTGACAGAGTGAAACTCCGTCTCAAAAAAAAAAAATAGATACTGT GCCACTTCACTCTAGCCTGGGTGACAGAGTGAGACTCCGTCTCAAAAAAAAAAAATAGATACTGT A G MYBL2 Ensembl:ENSG00000101057 Protein coding intron GSE100210 HepG2 cell line chr20:43672200..43672201 29129909 RNA-Seq:(High) rs532250652 Functional Loss SNV ICGC 33..33 33 PRAD 1 - Human_RBP_ID_14114411 RMVar_hsa_circ_96108,RMVar_hsa_circ_118554,RMVar_hsa_circ_210269,RMVar_hsa_circ_210270 54781 RMVar_ID_54781 Human_SNP_ID_842581826 A-to-I Human chr20 - 63793712 63793712 63793712 GTGAACCGTTGTGAGGTAGCCGCTGCTTCTATAAAATCTTACGTGGAGGTGTGGACCGTTGTGAG GTGAACCGTTGTGAGGTAGCCGCTGCTTCTATGAAATCTTACGTGGAGGTGTGGACCGTTGTGAG T C ZBTB46 Ensembl:ENSG00000130584 Protein coding intron GSE100210 HepG2 cell line chr20:63793711..63793712 29129909 RNA-Seq:(High) rs6062531 Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_17143372 54782 RMVar_ID_54782 Human_SNP_ID_842586206 A-to-I Human chr20 - 51857460 51857460 51857460 GGGTGTGGTGGTGCACAGCTGTATTCTCAGCTACTTGGGAGGCTGAGGCAGGAGAATTGCTTGAA GGGTGTGGTGGTGCACAGCTGTATTCTCAGCTGCTTGGGAGGCTGAGGCAGGAGAATTGCTTGAA T C LINC01429 Ensembl:ENSG00000227964 lincRNA intron GSE100210 HepG2 cell line chr20:51857459..51857460 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_210964 54783 RMVar_ID_54783 Human_SNP_ID_842639845 A-to-I Human chr20 + 56393378 56393378 56393378 CAGGATGTGCATGTAAAGCATTGAGCTAGCATACGGAAATTATTCGAGTCATATTAACCCAACGT CAGGATGTGCATGTAAAGCATTGAGCTAGCATGCGGAAATTATTCGAGTCATATTAACCCAACGT A G CSTF1 Ensembl:ENSG00000101138 Protein coding intron GSE100210 HepG2 cell line chr20:56393377..56393378 29129909 RNA-Seq:(High) rs531794012 Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 2 breast 54784 RMVar_ID_54784 Human_SNP_ID_842643736 A-to-I Human chr20 + 53293342 53293342 53293342 AAAATTAGCCAGGCCTGGTGGTGCAGGCCTGTAATCCCAGCCACTCGGGAGGCTGAGGCACGAGA AAAATTAGCCAGGCCTGGTGGTGCAGGCCTGTGATCCCAGCCACTCGGGAGGCTGAGGCACGAGA A G TSHZ2 Ensembl:ENSG00000182463 Protein coding intron GSE100210 HepG2 cell line chr20:53293341..53293342 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 54785 RMVar_ID_54785 Human_SNP_ID_842648948 A-to-I Human chr20 - 52078915 52078915 52078915 ATCCCACCTCAGCCTCCCGAGTAGCTGGGATTATAGGCACATGTCACCATGCCTGGCTAGTTTTT ATCCCACCTCAGCCTCCCGAGTAGCTGGGATTGTAGGCACATGTCACCATGCCTGGCTAGTTTTT T C ZFP64 Ensembl:ENSG00000020256 Protein coding intron GSE100210 HepG2 cell line chr20:52078914..52078915 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 54786 RMVar_ID_54786 Human_SNP_ID_842687082 A-to-I Human chr20 - 31285759 31285759 31285759 ACCCAGAATCAGTTCCTTGATGAGCTCATGGAACTTGAGATCTTCTTAGCCCAGAGAGCAGTGGA ACCCAGAATCAGTTCCTTGATGAGCTCATGGAGCTTGAGATCTTCTTAGCCCAGAGAGCAGTGGA T C AL121723.1 Ensembl:ENSG00000224628 Pseudogene exon GSE100210 HepG2 cell line chr20:31285758..31285759 29129909 RNA-Seq:(High) rs878878540 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_5594931 Human_miRNA_ID_1886524,Human_miRNA_ID_1886961 54787 RMVar_ID_54787 Human_SNP_ID_842704794 A-to-I Human chr20 - 49829598 49829598 49829598 TGAGCATGATATGGCTTCAGCTGTTTCACTTTAATCCAGGCATGATCTTATGTTCCAAAAAAATT TGAGCATGATATGGCTTCAGCTGTTTCACTTTGATCCAGGCATGATCTTATGTTCCAAAAAAATT T C - - Other Unknown GSE100210 HepG2 cell line chr20:49829597..49829598 29129909 RNA-Seq:(High) rs1048984553 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 haematopoietic and lymphoid tissue 54788 RMVar_ID_54788 Human_SNP_ID_842706340 A-to-I Human chr20 + 17976769 17976769 17976769 CTGCAACCTCCATCTCCTAGGTTCAAGCTATTATCTTGCCTCAGCCTCCCAAGTAGCTGGGATTA CTGCAACCTCCATCTCCTAGGTTCAAGCTATTGTCTTGCCTCAGCCTCCCAAGTAGCTGGGATTA A G MGME1 Ensembl:ENSG00000125871 Protein coding intron GSE100210 HepG2 cell line chr20:17976768..17976769 29129909 RNA-Seq:(High) rs1306313276 Functional Loss SNV ICGC 33..33 33 LICA 1 - 54789 RMVar_ID_54789 Human_SNP_ID_842759175 A-to-I Human chr20 - 31715264 31715264 31715264 CTGTATTCCTTTTTTTTTTTTTTTTGAGACAGAGTCTTTCTCTGTCTCCCAGACTGGAGTGCAGT CTGTATTCCTTTTTTTTTTTTTTTTGAGACAGGGTCTTTCTCTGTCTCCCAGACTGGAGTGCAGT T C BCL2L1 Ensembl:ENSG00000171552 Protein coding intron GSE100210 HepG2 cell line chr20:31715263..31715264 29129909 RNA-Seq:(High) rs1158485395 Functional Loss SNV ICGC 33..33 33 LICA 1 - 54790 RMVar_ID_54790 Human_SNP_ID_842773407 A-to-I Human chr20 + 62129116 62129116 62129116 GGTTCATCCCCTGTGCGTGGGCCTCGGACTGCAGTTTCATAGGCATAGCCCCTTGCCAAAGGCTA GGTTCATCCCCTGTGCGTGGGCCTCGGACTGCGGTTTCATAGGCATAGCCCCTTGCCAAAGGCTA A G LSM14B Ensembl:ENSG00000149657 Protein coding intron GSE100210 HepG2 cell line chr20:62129115..62129116 29129909 RNA-Seq:(High) rs564687440 Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 1 large intestine Human_RBP_ID_22601504 RMVar_hsa_circ_123618,RMVar_hsa_circ_120149,RMVar_hsa_circ_211148,RMVar_hsa_circ_281693,RMVar_hsa_circ_211151,RMVar_hsa_circ_211152 54791 RMVar_ID_54791 Human_SNP_ID_842809495 A-to-I Human chr20 - 49274507 49274507 49274507 GTGATCCACCCACCTTGGCCTCCCAAAGTGCTAGCATTACAGGCGTGAGCCACTGTGCCTGGCCT GTGATCCACCCACCTTGGCCTCCCAAAGTGCTGGCATTACAGGCGTGAGCCACTGTGCCTGGCCT T C ZNFX1 Ensembl:ENSG00000124201 Protein coding intron GSE38233 cultured B-cells chr20:49274506..49274507 24183664 RNA-Seq:(High) rs1200112295 Functional Loss SNV ICGC 33..33 33 ESCA 1 - 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 54792 RMVar_ID_54792 Human_SNP_ID_842816634 A-to-I Human chr20 - 3961254 3961254 3961254 GGGACTCTAGACACCCACCACCACACCCAGCTAATTTTTTTATTTTTTGTAGAGACGAAGTCTCA GGGACTCTAGACACCCACCACCACACCCAGCTTATTTTTTTATTTTTTGTAGAGACGAAGTCTCA T A RNF24 Ensembl:ENSG00000101236 Protein coding intron GSE100210 HepG2 cell line chr20:3961253..3961254 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - RMVar_hsa_circ_208526,RMVar_hsa_circ_280870,RMVar_hsa_circ_296842,RMVar_hsa_circ_208527,RMVar_hsa_circ_208529,RMVar_hsa_circ_208531,RMVar_hsa_circ_274265,RMVar_hsa_circ_287625,RMVar_hsa_circ_122559,RMVar_hsa_circ_208530,RMVar_hsa_circ_208533,RMVar_hsa_circ_328639,RMVar_hsa_circ_208528,RMVar_hsa_circ_278180,RMVar_hsa_circ_208532 54793 RMVar_ID_54793 Human_SNP_ID_842893338 A-to-I Human chr20 - 17962408 17962407 17962408 ACGAGGTCAGGAGTTAGAGACCAGCCTGACCAACATGGTGAAACCCTGTCTCTACTAAAAATACA ACGAGGTCAGGAGTTAGAGACCAGCCTGACCA_CATGGTGAAACCCTGTCTCTACTAAAAATACA GT G SNX5,OVOL2 Ensembl:ENSG00000089006,Ensembl:ENSG00000125850 Protein coding,Protein coding intron,intron GSE99789;GSE126723:GSM3611833,GSM3611834,GSM3611835 esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BERP35T4 cell line chr20:17962407..17962408 29796672,31158229 RNA-Seq:(High) rs11475300 Functional Loss DEL ICGC 33..33 33 ESCA 1 - 54794 RMVar_ID_54794 Human_SNP_ID_842904352 A-to-I Human chr20 + 30404754 30404754 30404754 TGGAAAGTGAGGAGCGTCTCTGCCCAGCCGCCATCCCATCTAGGAAGTGAGGAGCGTCTCTGCCC TGGAAAGTGAGGAGCGTCTCTGCCCAGCCGCCGTCCCATCTAGGAAGTGAGGAGCGTCTCTGCCC A G lnc-DEFB115-4,lnc-DEFB115-3,lnc-DEFB115-5,lnc-DEFB115-4:2 RNACentral:URS00008BE790,RNACentral:URS0000D5D40B,RNACentral:URS00008C33AD,RNACentral:URS00009B5876 lincRNA,lincRNA,lincRNA,lincRNA intron,exon,intron,intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr20:30404753..30404754 30559470 RNA-Seq:(High) rs532953935 Functional Loss SNV ICGC 33..33 33 PBCA 1 - 54795 RMVar_ID_54795 Human_SNP_ID_809945600 A-to-I Human chr11 - 61422490 61422489 61422490 CAACATGGTGAAACCCTGTCTCTACAAAAAAAATTTGAAAATTAGCTGGGCATGGTTGCGCATGT CAACATGGTGAAACCCTGTCTCTACAAAAAAA_TTTGAAAATTAGCTGGGCATGGTTGCGCATGT AT A CPSF7 Ensembl:ENSG00000149532 Protein coding intron GSE100210 HepG2 cell line chr11:61422489..61422490 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 33..33 33 ESCA 1 - 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 54796 RMVar_ID_54796 Human_SNP_ID_809946249 A-to-I Human chr11 + 64309387 64309387 64309387 CCGGGAGGCAGAGGTTGCAGTGAGCTGAGATCATGCCACAGCACTCTAGTCTGGGCAACAGAATG CCGGGAGGCAGAGGTTGCAGTGAGCTGAGATCGTGCCACAGCACTCTAGTCTGGGCAACAGAATG A G ESRRA Ensembl:ENSG00000173153 Protein coding intron GSE100210 HepG2 cell line chr11:64309386..64309387 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 54797 RMVar_ID_54797 Human_SNP_ID_810004243 A-to-I Human chr11 - 90283005 90283005 90283005 TGGTTAGCCAGCTTGCGAATTCGGTCCAACACAAGGTCAATGATCTCCTTGCCAATGGTGTAGTG TGGTTAGCCAGCTTGCGAATTCGGTCCAACACGAGGTCAATGATCTCCTTGCCAATGGTGTAGTG T C - - Other Unknown GSE100210 HepG2 cell line chr11:90283004..90283005 29129909 RNA-Seq:(High) rs878865124 Functional Loss SNV ICGC 33..33 33 LICA 1 - 54798 RMVar_ID_54798 Human_SNP_ID_810035043 A-to-I Human chr11 - 124757865 124757864 124757865 GTGAAACCCCCGTCTCTGCTAAAAACACAAAAATTAGTCGGACATGGTGGCACCCGCCTGTAATC GTGAAACCCCCGTCTCTGCTAAAAACACAAAA_TTAGTCGGACATGGTGGCACCCGCCTGTAATC AT A ESAM Ensembl:ENSG00000149564 Protein coding intron GSE47997 K562 cells&HepG2 cells chr11:124757864..124757865 23474544 RNA-Seq:(High) - Functional Loss DEL ICGC 33..33 33 PAAD 1 - 54799 RMVar_ID_54799 Human_SNP_ID_810042238 A-to-I Human chr11 - 76377382 76377382 76377382 AAGGGAGAGTGGGGAGCAACTGATTAATGGTTACAAGGTTTCCTTTTGAGGTGATGAAAATGTTT AAGGGAGAGTGGGGAGCAACTGATTAATGGTTGCAAGGTTTCCTTTTGAGGTGATGAAAATGTTT T C THAP12 Ensembl:ENSG00000137492 Protein coding intron GSE47997 K562 cells&HepG2 cells chr11:76377381..76377382 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 54800 RMVar_ID_54800 Human_SNP_ID_810063459 A-to-I Human chr11 - 74042077 74042077 74042077 GACAAACTGACCACATCACCTTTGTCCTCCCAAACCTCCATTCTGACTTCTCTCAGGTGAGGCTC GACAAACTGACCACATCACCTTTGTCCTCCCACACCTCCATTCTGACTTCTCTCAGGTGAGGCTC T G C2CD3 Ensembl:ENSG00000168014 Protein coding CDS GSE100210 HepG2 cell line chr11:74042076..74042077 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA 33..33 33 READ 1 - Human_Splice_Rec_1277173,Human_Splice_Rec_1277197,Human_Splice_Rec_1277211,Human_Splice_Rec_1277215,Human_Splice_Rec_1277275,Human_Splice_Rec_1277297,Human_Splice_Rec_1277305 RMVar_hsa_circ_43465,RMVar_hsa_circ_90008,RMVar_hsa_circ_151658,RMVar_hsa_circ_70208,RMVar_hsa_circ_355710,RMVar_hsa_circ_151659,RMVar_hsa_circ_44947,RMVar_hsa_circ_100073,RMVar_hsa_circ_95330,RMVar_hsa_circ_113937,RMVar_hsa_circ_13125,RMVar_hsa_circ_111963,RMVar_hsa_circ_151663,RMVar_hsa_circ_151665,RMVar_hsa_circ_78234,RMVar_hsa_circ_151664,RMVar_hsa_circ_151662,RMVar_hsa_circ_14161,RMVar_hsa_circ_96547,RMVar_hsa_circ_151666,RMVar_hsa_circ_151667 54801 RMVar_ID_54801 Human_SNP_ID_810064516 A-to-I Human chr11 - 47790659 47790659 47790659 GCCTCAAACTCCTGGACTCAAGCAATCCTCCTACCTCGGACTCCCACAGTGCTGGGACTACAGGG GCCTCAAACTCCTGGACTCAAGCAATCCTCCTTCCTCGGACTCCCACAGTGCTGGGACTACAGGG T A NUP160 Ensembl:ENSG00000030066 Protein coding intron GSE100210 HepG2 cell line chr11:47790658..47790659 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_17559960 RMVar_hsa_circ_364147,RMVar_hsa_circ_373104,RMVar_hsa_circ_352463,RMVar_hsa_circ_42816,RMVar_hsa_circ_51616,RMVar_hsa_circ_31768,RMVar_hsa_circ_62759,RMVar_hsa_circ_149652,RMVar_hsa_circ_109870,RMVar_hsa_circ_50527,RMVar_hsa_circ_149657,RMVar_hsa_circ_149658,RMVar_hsa_circ_149656,RMVar_hsa_circ_47121,RMVar_hsa_circ_28477,RMVar_hsa_circ_104454,RMVar_hsa_circ_319393,RMVar_hsa_circ_340051,RMVar_hsa_circ_342040,RMVar_hsa_circ_302165,RMVar_hsa_circ_92217,RMVar_hsa_circ_102271,RMVar_hsa_circ_45602,RMVar_hsa_circ_149662,RMVar_hsa_circ_149664,RMVar_hsa_circ_149665,RMVar_hsa_circ_149666,RMVar_hsa_circ_149663,RMVar_hsa_circ_149661,RMVar_hsa_circ_285620 54802 RMVar_ID_54802 Human_SNP_ID_810087178 A-to-I Human chr11 + 18360988 18360988 18360988 CTGCCACGCCCAGCTAATTTTTGTATTTTAGTAGAGACGGGGTTTCACCATGTTGGCCAGGCTGG CTGCCACGCCCAGCTAATTTTTGTATTTTAGTGGAGACGGGGTTTCACCATGTTGGCCAGGCTGG A G GTF2H1 Ensembl:ENSG00000110768 Protein coding intron GSE38233 cultured B-cells chr11:18360987..18360988 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 UTCA 1 - 54803 RMVar_ID_54803 Human_SNP_ID_810111459 A-to-I Human chr11 - 90283048 90283048 90283048 ACCAAAGCTGTGGAAAACCAAGAAGCCCTGAAAACCAGTGCACTGGTTAGCCAGCTTGCGAATTC ACCAAAGCTGTGGAAAACCAAGAAGCCCTGAAGACCAGTGCACTGGTTAGCCAGCTTGCGAATTC T C - - Other Unknown GSE100210 HepG2 cell line chr11:90283047..90283048 29129909 RNA-Seq:(High) rs879097595 Functional Loss SNV ICGC 33..33 33 LAML 2 - 54804 RMVar_ID_54804 Human_SNP_ID_810136024 A-to-I Human chr11 + 47217120 47217120 47217120 TTTGTTGGCTGGGTGCAGTGGTTCGCACCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGGTGG TTTGTTGGCTGGGTGCAGTGGTTCGCACCTGTGATCCCAGCACTTTGGGAGGCCAAGGTGGGTGG A G DDB2 Ensembl:ENSG00000134574 Protein coding intron GSE38233 cultured B-cells chr11:47217119..47217120 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_115720,RMVar_hsa_circ_341997,RMVar_hsa_circ_312085,RMVar_hsa_circ_121105,RMVar_hsa_circ_298445,RMVar_hsa_circ_149496,RMVar_hsa_circ_149497,RMVar_hsa_circ_149499,RMVar_hsa_circ_111960,RMVar_hsa_circ_149498 54805 RMVar_ID_54805 Human_SNP_ID_810164938 A-to-I Human chr11 - 61413200 61413200 61413200 GAAAGTCTCATGAGGTACAGTGGCTCATACCTATAATCCCAGCACTTTAGGAGGCCCAGGCAGGA GAAAGTCTCATGAGGTACAGTGGCTCATACCTGTAATCCCAGCACTTTAGGAGGCCCAGGCAGGA T C CPSF7 Ensembl:ENSG00000149532 Protein coding intron GSE38233 cultured B-cells chr11:61413199..61413200 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_24891638 RMVar_hsa_circ_20775,RMVar_hsa_circ_150021,RMVar_hsa_circ_116705,RMVar_hsa_circ_325034,RMVar_hsa_circ_341262,RMVar_hsa_circ_333194,RMVar_hsa_circ_150023,RMVar_hsa_circ_63858,RMVar_hsa_circ_150024,RMVar_hsa_circ_150022,RMVar_hsa_circ_101153,RMVar_hsa_circ_339353,RMVar_hsa_circ_150026 54806 RMVar_ID_54806 Human_SNP_ID_810240014 A-to-I Human chr11 - 47635965 47635965 47635965 CGCCCCAATGCTCCGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGC CGCCCCAATGCTCCGCTAATTTTTGTATTTTTCGTAGAGATGGGGTTTCACCATGTTGGCCAGGC T G MTCH2 Ensembl:ENSG00000109919 Protein coding intron GSE38233 cultured B-cells chr11:47635964..47635965 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_149608,RMVar_hsa_circ_304166,RMVar_hsa_circ_331910,RMVar_hsa_circ_149610,RMVar_hsa_circ_92371,RMVar_hsa_circ_122903,RMVar_hsa_circ_149615,RMVar_hsa_circ_149616,RMVar_hsa_circ_296967 54807 RMVar_ID_54807 Human_SNP_ID_810347616 A-to-I Human chr11 - 123080593 123080593 123080593 TCGAGGCGCAGTGGCTCACACCTGTAATCCCAACACTTTGGGAGGCCAAGGCGGGCAGATCACTT TCGAGGCGCAGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGCGGGCAGATCACTT T C CLMP Ensembl:ENSG00000166250 Protein coding intron GSE100210 HepG2 cell line chr11:123080592..123080593 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 1 prostate RMVar_hsa_circ_18586 54808 RMVar_ID_54808 Human_SNP_ID_810423551 A-to-I Human chr11 - 127941471 127941471 127941471 GGCATATGAAGTGCTGTCGGATGCTAAGAAACAGGACATCTATGACAAATATGGCAAAGAAGGAT GGCATATGAAGTGCTGTCGGATGCTAAGAAACGGGACATCTATGACAAATATGGCAAAGAAGGAT T C AP001000.1 Ensembl:ENSG00000254612 Pseudogene exon GSE100210 HepG2 cell line chr11:127941470..127941471 29129909 RNA-Seq:(High) rs571669348 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_4152788,Human_RBP_ID_26402165 Human_miRNA_ID_1866718,Human_miRNA_ID_1866998 54809 RMVar_ID_54809 Human_SNP_ID_810479401 A-to-I Human chr11 - 91114774 91114774 91114774 GGAGACAAGGTTATTTCATAAAGATGGAGAATATTGGGTTTATGATGAACCATTACTGAAATATC GGAGACAAGGTTATTTCATAAAGATGGAGAATGTTGGGTTTATGATGAACCATTACTGAAATATC T C OSBPL9P2 Ensembl:ENSG00000254677 Pseudogene exon GSE100210 HepG2 cell line chr11:91114773..91114774 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 NKTL 1 - 54810 RMVar_ID_54810 Human_SNP_ID_810525306 A-to-I Human chr11 - 68900420 68900420 68900420 TATTTAAATTTCCTCTTTTGTTTTTAAGAGACAGAGTTTCACTATGTTTCCCAGACTGGTTTTGA TATTTAAATTTCCTCTTTTGTTTTTAAGAGACGGAGTTTCACTATGTTTCCCAGACTGGTTTTGA T C MRPL21 Ensembl:ENSG00000197345 Protein coding intron GSE100210 HepG2 cell line chr11:68900419..68900420 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue RMVar_hsa_circ_68010,RMVar_hsa_circ_111187,RMVar_hsa_circ_151323 54811 RMVar_ID_54811 Human_SNP_ID_810615456 A-to-I Human chr11 - 3794860 3794860 3794860 TACTGTAATCCCAGCACTTCAAAGGTCAAGGCAGGTGGATTTCCTGAGCCCAGAAGTTCAAGACT TACTGTAATCCCAGCACTTCAAAGGTCAAGGCTGGTGGATTTCCTGAGCCCAGAAGTTCAAGACT T A NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line chr11:3794859..3794860 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 6 ovary Human_RBP_ID_9639493 RMVar_hsa_circ_125448,RMVar_hsa_circ_147660,RMVar_hsa_circ_128055,RMVar_hsa_circ_147669,RMVar_hsa_circ_92246,RMVar_hsa_circ_147707 54812 RMVar_ID_54812 Human_SNP_ID_810616563 A-to-I Human chr11 - 66520807 66520807 66520807 ACTGTTTGAGCCCAGGTGGCATAGGTTGCAGTAAGCTGAGATTGTACCACTGCACTTCAGCCTGG ACTGTTTGAGCCCAGGTGGCATAGGTTGCAGTGAGCTGAGATTGTACCACTGCACTTCAGCCTGG T C ZDHHC24 Ensembl:ENSG00000174165 Protein coding 3'UTR GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line chr11:66520806..66520807 24183664,31158229 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 12 haematopoietic and lymphoid tissue 54813 RMVar_ID_54813 Human_SNP_ID_810623866 A-to-I Human chr11 - 16789212 16789212 16789212 AGATGAGTGCAGAGGAGCAGCTGGAGCGCATGAAGCGACACCAGAAGGCCCTGGTCCGAGAGCGC AGATGAGTGCAGAGGAGCAGCTGGAGCGCATGTAGCGACACCAGAAGGCCCTGGTCCGAGAGCGC T A PLEKHA7 Ensembl:ENSG00000166689 Protein coding CDS GSE47997 K562 cells&HepG2 cells chr11:16789211..16789212 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LUSC 2 - Human_RBP_ID_18973353 Human_Splice_Rec_1214114,Human_Splice_Rec_1214134,Human_Splice_Rec_1214180,Human_Splice_Rec_1214190,Human_Splice_Rec_1214238,Human_Splice_Rec_1214248,Human_Splice_Rec_1214274,Human_Splice_Rec_1214298,Human_Splice_Rec_1214322,Human_Splice_Rec_1214326,Human_Splice_Rec_1214328 RMVar_hsa_circ_148420,RMVar_hsa_circ_90941,RMVar_hsa_circ_111264,RMVar_hsa_circ_118480,RMVar_hsa_circ_118876,RMVar_hsa_circ_113097,RMVar_hsa_circ_107187,RMVar_hsa_circ_101819,RMVar_hsa_circ_102047,RMVar_hsa_circ_98496,RMVar_hsa_circ_148424,RMVar_hsa_circ_148428,RMVar_hsa_circ_87024,RMVar_hsa_circ_88305,RMVar_hsa_circ_82968,RMVar_hsa_circ_148426,RMVar_hsa_circ_148427,RMVar_hsa_circ_148425,RMVar_hsa_circ_148422,RMVar_hsa_circ_148423,RMVar_hsa_circ_148421,RMVar_hsa_circ_24296,RMVar_hsa_circ_148418,RMVar_hsa_circ_148419,RMVar_hsa_circ_148417 54814 RMVar_ID_54814 Human_SNP_ID_810717980 A-to-I Human chr11 + 57720603 57720603 57720603 TTGTATTTTAGTGGAGACAGTTTCACCACGTTAGTTAGGCTGATCTCGAACTTCTGGCCTCAAGC TTGTATTTTAGTGGAGACAGTTTCACCACGTTTGTTAGGCTGATCTCGAACTTCTGGCCTCAAGC A T AP001931.2,TMX2 Ensembl:ENSG00000288534,Ensembl:ENSG00000213593 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line chr11:57720602..57720603 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 3 breast Human_RBP_ID_11643536 RMVar_hsa_circ_123482,RMVar_hsa_circ_149806,RMVar_hsa_circ_83957,RMVar_hsa_circ_149805 54815 RMVar_ID_54815 Human_SNP_ID_810795263 A-to-I Human chr11 - 61814052 61814052 61814052 TTATTGTGAAGAGCAAAGAACAAAGCTTCCACAGCGTGGAAGGGTACCCGAGCAGGTTGCCGCTG TTATTGTGAAGAGCAAAGAACAAAGCTTCCACGGCGTGGAAGGGTACCCGAGCAGGTTGCCGCTG T C FADS1 Ensembl:ENSG00000149485 Protein coding intron GSE100210 HepG2 cell line chr11:61814051..61814052 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 54816 RMVar_ID_54816 Human_SNP_ID_810848546 A-to-I Human chr11 - 59131034 59131034 59131034 TTATTGTCGGTATCACTATCACATTTTGGGCAAAGGCATTCGACAAGTCTCTATGAAGTTCCAAA TTATTGTCGGTATCACTATCACATTTTGGGCAGAGGCATTCGACAAGTCTCTATGAAGTTCCAAA T C FAM111A-DT Ensembl:ENSG00000245571 lincRNA intron GSE100210 HepG2 cell line chr11:59131033..59131034 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 RECA 1 - 54817 RMVar_ID_54817 Human_SNP_ID_810853136 A-to-I Human chr11 + 63821852 63821852 63821852 CTCACTGCAACCTCAAACTCCCAGGCTCAAGCAGTCCTCCTGCCACAGCCTCCTGAGTAGCTGGG CTCACTGCAACCTCAAACTCCCAGGCTCAAGCCGTCCTCCTGCCACAGCCTCCTGAGTAGCTGGG A C SPINDOC Ensembl:ENSG00000168005 Protein coding intron GSE38233 cultured B-cells chr11:63821851..63821852 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - RMVar_hsa_circ_78377,RMVar_hsa_circ_150371,RMVar_hsa_circ_97315,RMVar_hsa_circ_150372,RMVar_hsa_circ_150378,RMVar_hsa_circ_101809 54818 RMVar_ID_54818 Human_SNP_ID_810866341 A-to-I Human chr11 - 123599054 123599054 123599054 GAGGCACAAAACTCGGTGGAGTTCACAGATGAAGAGGGATATGGTCGTTACCTCGATCTCCATGA GAGGCACAAAACTCGGTGGAGTTCACAGATGAGGAGGGATATGGTCGTTACCTCGATCTCCATGA T C SF3A3P2 Ensembl:ENSG00000254449 Pseudogene exon GSE38233 cultured B-cells chr11:123599053..123599054 24183664 RNA-Seq:(High) rs879010397 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 18 haematopoietic and lymphoid tissue Human_RBP_ID_18526187 54819 RMVar_ID_54819 Human_SNP_ID_810884946 A-to-I Human chr11 + 119004962 119004962 119004962 TTTGCCTGTAGTGCTAGCTACTGGGGAGGCTGAGGCAGGAGGATTGCTTAAGCTCACAAGGTTGA TTTGCCTGTAGTGCTAGCTACTGGGGAGGCTGTGGCAGGAGGATTGCTTAAGCTCACAAGGTTGA A T CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE100210 HepG2 cell line chr11:119004961..119004962 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_17560167,Human_RBP_ID_22570244 RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 54820 RMVar_ID_54820 Human_SNP_ID_810898886 A-to-I Human chr11 + 77025548 77025548 77025548 CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTACAGGCACATGCCACCATGCCACCATGCCTGGC CTCCTGCCTCAGCCTCCCGAGTAGCTGGGACTGCAGGCACATGCCACCATGCCACCATGCCTGGC A G ACER3 Ensembl:ENSG00000078124 Protein coding 3'UTR GSE100210 HepG2 cell line chr11:77025547..77025548 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 54821 RMVar_ID_54821 Human_SNP_ID_810908510 A-to-I Human chr11 - 61813508 61813508 61813508 TTACAAACCTCTAGCTACAGAAAAGTTCTCCAAGTCTGCACTCGACCCAGGAAGTCCATCTGGCT TTACAAACCTCTAGCTACAGAAAAGTTCTCCACGTCTGCACTCGACCCAGGAAGTCCATCTGGCT T G FADS1 Ensembl:ENSG00000149485 Protein coding intron GSE47997;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 K562 cells&HepG2 cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line chr11:61813507..61813508 23474544,29129909,31158229 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 RECA 1 - Human_RBP_ID_17560323,Human_RBP_ID_22569227 Human_Splice_Rec_1246932,Human_Splice_Rec_1246954,Human_Splice_Rec_1246955,Human_Splice_Rec_1246958 54822 RMVar_ID_54822 Human_SNP_ID_810930151 A-to-I Human chr11 - 73031354 73031354 73031354 CTCCCACCTCAGCCTCCCGAGTAGCTGGGACTACAGGCACACACCACCACACCAGGCTAATTTTT CTCCCACCTCAGCCTCCCGAGTAGCTGGGACTGCAGGCACACACCACCACACCAGGCTAATTTTT T C FCHSD2 Ensembl:ENSG00000137478 Protein coding intron GSE100210 HepG2 cell line chr11:73031353..73031354 29129909 RNA-Seq:(High) rs1370333790 Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 6 prostate RMVar_hsa_circ_151592,RMVar_hsa_circ_30655,RMVar_hsa_circ_282614,RMVar_hsa_circ_151591,RMVar_hsa_circ_151594,RMVar_hsa_circ_275444,RMVar_hsa_circ_63691 54823 RMVar_ID_54823 Human_SNP_ID_811008084 A-to-I Human chr11 + 48009511 48009511 48009511 CCAGCTACTCAGGGGTCTGAGGCAGAAGGATCACTTGAACCTGGGAGGCGGAGGGTGTAGCGAGC CCAGCTACTCAGGGGTCTGAGGCAGAAGGATCTCTTGAACCTGGGAGGCGGAGGGTGTAGCGAGC A T PTPRJ Ensembl:ENSG00000149177 Protein coding intron GSE107867 ASD brains,temporal_cortex chr11:48009510..48009511 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 5 liver 54824 RMVar_ID_54824 Human_SNP_ID_811011695 A-to-I Human chr11 - 47799812 47799812 47799812 AGTGGGTGCAGTGGCTCACGCCTGTAATCCCAACACTTTGAGAGGCTAAGGCAGGAGGATCACTG AGTGGGTGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGAGAGGCTAAGGCAGGAGGATCACTG T C NUP160 Ensembl:ENSG00000030066 Protein coding intron GSE38233 cultured B-cells chr11:47799811..47799812 24183664 RNA-Seq:(High) rs998097345 Functional Loss SNV ICGC 33..33 33 BOCA 1 - RMVar_hsa_circ_373104,RMVar_hsa_circ_352463,RMVar_hsa_circ_42816,RMVar_hsa_circ_51616,RMVar_hsa_circ_31768,RMVar_hsa_circ_62759,RMVar_hsa_circ_149652,RMVar_hsa_circ_109870,RMVar_hsa_circ_50527,RMVar_hsa_circ_149657,RMVar_hsa_circ_149658,RMVar_hsa_circ_47121,RMVar_hsa_circ_27747,RMVar_hsa_circ_28477,RMVar_hsa_circ_104454,RMVar_hsa_circ_319393,RMVar_hsa_circ_340051,RMVar_hsa_circ_302165,RMVar_hsa_circ_92217,RMVar_hsa_circ_102271,RMVar_hsa_circ_45602,RMVar_hsa_circ_149662,RMVar_hsa_circ_149664,RMVar_hsa_circ_149665,RMVar_hsa_circ_149666,RMVar_hsa_circ_149663,RMVar_hsa_circ_115231,RMVar_hsa_circ_90337,RMVar_hsa_circ_345496,RMVar_hsa_circ_317760,RMVar_hsa_circ_149667,RMVar_hsa_circ_149668,RMVar_hsa_circ_117638,RMVar_hsa_circ_149671,RMVar_hsa_circ_94554,RMVar_hsa_circ_149673,RMVar_hsa_circ_57124,RMVar_hsa_circ_149672,RMVar_hsa_circ_285232,RMVar_hsa_circ_313095,RMVar_hsa_circ_294432,RMVar_hsa_circ_103615,RMVar_hsa_circ_119511,RMVar_hsa_circ_149675,RMVar_hsa_circ_149676,RMVar_hsa_circ_149677,RMVar_hsa_circ_106379,RMVar_hsa_circ_35496,RMVar_hsa_circ_149679,RMVar_hsa_circ_149680,RMVar_hsa_circ_149681,RMVar_hsa_circ_59503,RMVar_hsa_circ_11887 54825 RMVar_ID_54825 Human_SNP_ID_811016531 A-to-I Human chr11 + 93761812 93761812 93761812 ATCCCACAGGCCAGGCACAATGGCTCATGCCTATAATCCCAGCACTTTGGGAGGCTGAGGCAGGA ATCCCACAGGCCAGGCACAATGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGCAGGA A G AP001273.2,C11orf54 Ensembl:ENSG00000284057,Ensembl:ENSG00000182919 Protein coding,Protein coding intron,3'UTR GSE38233;GSE100210;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line chr11:93761811..93761812 24183664,29129909,29796672,31158229 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 8 haematopoietic and lymphoid tissue RMVar_hsa_circ_58230 54826 RMVar_ID_54826 Human_SNP_ID_811055948 A-to-I Human chr11 - 9835537 9835537 9835537 GCCTCAACCTCCCTGGCTCAGGCGATCCTTCCACCTCAGCTTTCTGAGTAGCTGGGACTAGGCGC GCCTCAACCTCCCTGGCTCAGGCGATCCTTCCCCCTCAGCTTTCTGAGTAGCTGGGACTAGGCGC T G SBF2 Ensembl:ENSG00000133812 Protein coding intron GSE100210 HepG2 cell line chr11:9835536..9835537 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 3 pancreas RMVar_hsa_circ_91477,RMVar_hsa_circ_148124,RMVar_hsa_circ_94571,RMVar_hsa_circ_118501,RMVar_hsa_circ_148126,RMVar_hsa_circ_148128,RMVar_hsa_circ_10524,RMVar_hsa_circ_297660,RMVar_hsa_circ_148134,RMVar_hsa_circ_79433,RMVar_hsa_circ_38103,RMVar_hsa_circ_148138,RMVar_hsa_circ_76380,RMVar_hsa_circ_148137,RMVar_hsa_circ_349568,RMVar_hsa_circ_123216,RMVar_hsa_circ_303694,RMVar_hsa_circ_100032,RMVar_hsa_circ_72355,RMVar_hsa_circ_2402,RMVar_hsa_circ_4481,RMVar_hsa_circ_148139,RMVar_hsa_circ_148140,RMVar_hsa_circ_52466 54827 RMVar_ID_54827 Human_SNP_ID_811061886 A-to-I Human chr11 + 18398753 18398753 18398753 CTCCTGTCTCAGCCTCCCAAGTAGCTGGGACTACAGGCACCCACCACCACGCCTGGCTAAATGTT CTCCTGTCTCAGCCTCCCAAGTAGCTGGGACTGCAGGCACCCACCACCACGCCTGGCTAAATGTT A G LDHA Ensembl:ENSG00000134333 Protein coding intron GSE38233 cultured B-cells chr11:18398752..18398753 24183664 RNA-Seq:(High) rs7117399 Functional Loss SNV ICGC 33..33 33 COCA 2 - RMVar_hsa_circ_91084,RMVar_hsa_circ_114054,RMVar_hsa_circ_148591,RMVar_hsa_circ_148592,RMVar_hsa_circ_148593,RMVar_hsa_circ_108242 54828 RMVar_ID_54828 Human_SNP_ID_811069573 A-to-I Human chr11 + 119001801 119001801 119001801 TGAAACTGCCAGATGTGGTGGTGCACACCTGTAGTCCTAGCTACTCAGGAGGCTGAGGTAAGAGG TGAAACTGCCAGATGTGGTGGTGCACACCTGTGGTCCTAGCTACTCAGGAGGCTGAGGTAAGAGG A G CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE47997;GSE38233;GSE100210;GSE99789;GSE126723:GSM3611830,GSM3611831,GSM3611832 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BERP35T1 cell line chr11:119001800..119001801 23474544,24183664,29129909,29796672,31158229 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue Human_RBP_ID_11540682 Human_Splice_Rec_1305777 RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 54829 RMVar_ID_54829 Human_SNP_ID_811081003 A-to-I Human chr11 - 69665892 69665892 69665892 CGTCCACCTACCAAAGTGCTGGAATTGCAGGCATGAGCCACCACTCCCGGCCTGCTTTTTGTTTT CGTCCACCTACCAAAGTGCTGGAATTGCAGGCGTGAGCCACCACTCCCGGCCTGCTTTTTGTTTT T C LTO1 Ensembl:ENSG00000149716 Protein coding intron GSE100210 HepG2 cell line chr11:69665891..69665892 29129909 RNA-Seq:(High) rs1162000436 Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 4 ovary RMVar_hsa_circ_48671,RMVar_hsa_circ_40424,RMVar_hsa_circ_151350 54830 RMVar_ID_54830 Human_SNP_ID_811128201 A-to-I Human chr11 - 130001076 130001076 130001076 TTTAGGAGACAGGGTCTCTGGTTGCCCAGGCTAGAGTGCAGTGGCGCGATCTTGGCTCACTGCCG TTTAGGAGACAGGGTCTCTGGTTGCCCAGGCTGGAGTGCAGTGGCGCGATCTTGGCTCACTGCCG T C PRDM10 Ensembl:ENSG00000170325 Protein coding intron GSE100210 HepG2 cell line chr11:130001075..130001076 29129909 RNA-Seq:(High) rs1233330450 Functional Loss SNV ICGC 33..33 33 LICA 1 - 54831 RMVar_ID_54831 Human_SNP_ID_811185014 A-to-I Human chr11 + 62794044 62794044 62794044 AATAATAAAATAAAATAAGGTGGCACATGCCTATAGGCCCAGCTACTCTGGAGGCTGAGGTGGGA AATAATAAAATAAAATAAGGTGGCACATGCCTTTAGGCCCAGCTACTCTGGAGGCTGAGGTGGGA A T - - Other Unknown GSE100210 HepG2 cell line chr11:62794043..62794044 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 54832 RMVar_ID_54832 Human_SNP_ID_811219124 A-to-I Human chr11 + 34094690 34094689 34094690 GAGGTGGTGAATGCCTGTAGTTGTAGCTACTCAGGAGGCTAAGGCCGGAGGATCACTTGAGCCCA GAGGTGGTGAATGCCTGTAGTTGTAGCTACTTTGGAGGCTAAGGCCGGAGGATCACTTGAGCCCA CA TT CAPRIN1 Ensembl:ENSG00000135387 Protein coding intron GSE100210 HepG2 cell line chr11:34094689..34094690 29129909 RNA-Seq:(High) - Functional Loss MNV ICGC 32..33 33 MELA 1 - Human_RBP_ID_11606659,Human_RBP_ID_17559649,Human_RBP_ID_24883382 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_148993,RMVar_hsa_circ_148992,RMVar_hsa_circ_357235,RMVar_hsa_circ_86955,RMVar_hsa_circ_149002,RMVar_hsa_circ_306085,RMVar_hsa_circ_74569,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_149022,RMVar_hsa_circ_82654,RMVar_hsa_circ_149021,RMVar_hsa_circ_335867,RMVar_hsa_circ_99463,RMVar_hsa_circ_149028,RMVar_hsa_circ_115368,RMVar_hsa_circ_149031,RMVar_hsa_circ_30298,RMVar_hsa_circ_371871,RMVar_hsa_circ_84783,RMVar_hsa_circ_149034,RMVar_hsa_circ_149035 54833 RMVar_ID_54833 Human_SNP_ID_811264919 A-to-I Human chr11 - 94417288 94417287 94417288 AAATCCATTCTTAGAAAAAAACTGAGTAAAAAAGTATCTCAATGGGCTGGGTGCAGTGGCTCATG AAATCCATTCTTAGAAAAAAACTGAGTAAAAA_GTATCTCAATGGGCTGGGTGCAGTGGCTCATG CT C MRE11 Ensembl:ENSG00000020922 Protein coding 3'UTR GSE100210 HepG2 cell line chr11:94417287..94417288 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 33..33 33 LICA 1 - 54834 RMVar_ID_54834 Human_SNP_ID_811275835 A-to-I Human chr11 + 57719724 57719724 57719724 TTTTTTGTAGAGATGGGGTTTCGCCATGTTGCACAGGCTGATCTTGAACTCCTGGGCTCAAGTGG TTTTTTGTAGAGATGGGGTTTCGCCATGTTGCTCAGGCTGATCTTGAACTCCTGGGCTCAAGTGG A T AP001931.2,TMX2 Ensembl:ENSG00000288534,Ensembl:ENSG00000213593 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line chr11:57719723..57719724 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 3 liver RMVar_hsa_circ_123482,RMVar_hsa_circ_149806,RMVar_hsa_circ_83957,RMVar_hsa_circ_149805 54835 RMVar_ID_54835 Human_SNP_ID_811286336 A-to-I Human chr11 - 18665279 18665279 18665279 TTTTTCACCATTGGACAGTTCCACTCTTACACAGCAGCCACATAGTGTTCTTCCATTTAGCTCTC TTTTTCACCATTGGACAGTTCCACTCTTACACGGCAGCCACATAGTGTTCTTCCATTTAGCTCTC T C - - Other Unknown GSE38233 cultured B-cells chr11:18665278..18665279 24183664 RNA-Seq:(High) rs879073273 Functional Loss SNV ICGC 33..33 33 LAML 2 - 54836 RMVar_ID_54836 Human_SNP_ID_811288534 A-to-I Human chr11 + 1448505 1448505 1448505 TGCCCCAGCAACTGTAGCTCAGTGTTCCCAGCAGCTGCCTGGCCGGATAGGACCAGGGCTCGGCC TGCCCCAGCAACTGTAGCTCAGTGTTCCCAGCCGCTGCCTGGCCGGATAGGACCAGGGCTCGGCC A C BRSK2 Ensembl:ENSG00000174672 Protein coding intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr11:1448504..1448505 30559470 RNA-Seq:(High) rs1445272385 Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_266764 54837 RMVar_ID_54837 Human_SNP_ID_811292263 A-to-I Human chr11 - 17084754 17084754 17084754 TGGATCAGGGCTGGGTGCGGTGGCTCACCCCTATAATCCCAGCACTTTGGGAGGCCGAGGCAGGC TGGATCAGGGCTGGGTGCGGTGGCTCACCCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGC T C PIK3C2A Ensembl:ENSG00000011405 Protein coding intron GSE100210 HepG2 cell line chr11:17084753..17084754 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 54838 RMVar_ID_54838 Human_SNP_ID_811336936 A-to-I Human chr11 + 65323802 65323802 65323802 CCTCAGCCTCCCAAAGTGCTGGTATTACAGGCATGAGCCACCATGCCCGTCCAGGAAAGGTGTTA CCTCAGCCTCCCAAAGTGCTGGTATTACAGGCCTGAGCCACCATGCCCGTCCAGGAAAGGTGTTA A C AP000944.5 Ensembl:ENSG00000285816 Protein coding intron GSE100210 HepG2 cell line chr11:65323801..65323802 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 54839 RMVar_ID_54839 Human_SNP_ID_811350758 A-to-I Human chr11 + 46617585 46617585 46617585 GGCCATTACCGAAGCGGATGAAAACAAACACTAACGATGGCGGCGCCGGGAAGCGACCGGCTGCT GGCCATTACCGAAGCGGATGAAAACAAACACTGACGATGGCGGCGCCGGGAAGCGACCGGCTGCT A G ATG13 Ensembl:ENSG00000175224 Protein coding 5'UTR GSE100210 HepG2 cell line chr11:46617584..46617585 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_4186583,Human_RBP_ID_18608082 RMVar_hsa_circ_149380,RMVar_hsa_circ_81584 54840 RMVar_ID_54840 Human_SNP_ID_811370578 A-to-I Human chr11 - 101356984 101356984 101356984 TAAAGAACTACCTGAGACTGGGTACTTTATAAAGAAAAGGTGTTTAATTGGCTCACAGTTCCACA TAAAGAACTACCTGAGACTGGGTACTTTATAATGAAAAGGTGTTTAATTGGCTCACAGTTCCACA T A - - Other Unknown GSE100210 HepG2 cell line chr11:101356983..101356984 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 54841 RMVar_ID_54841 Human_SNP_ID_811377665 A-to-I Human chr11 + 100337209 100337209 100337209 GACACAGATGACACCAGCAGTGAAAACACTGTAGTTCCTCCAGAAACATATGTGAAAGTGGCAGG GACACAGATGACACCAGCAGTGAAAACACTGTGGTTCCTCCAGAAACATATGTGAAAGTGGCAGG A G RPA2P3,CNTN5 Ensembl:ENSG00000255547,Ensembl:ENSG00000149972 Pseudogene,Protein coding exon,intron GSE100210 HepG2 cell line chr11:100337208..100337209 29129909 RNA-Seq:(High) rs878874454 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 6 haematopoietic and lymphoid tissue Human_miRNA_ID_1827262,Human_miRNA_ID_1887559,Human_miRNA_ID_1909039 RMVar_hsa_circ_23698 54842 RMVar_ID_54842 Human_SNP_ID_811387070 A-to-I Human chr11 + 67039156 67039156 67039156 AGAAACCCTGTCTCTACTAAAAATACAAAATTAGCCGGGCGTGGTGGTGTGCACCTGTAATCCCG AGAAACCCTGTCTCTACTAAAAATACAAAATTCGCCGGGCGTGGTGGTGTGCACCTGTAATCCCG A C SYT12 Ensembl:ENSG00000173227 Protein coding intron GSE100210 HepG2 cell line chr11:67039155..67039156 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 4 breast 54843 RMVar_ID_54843 Human_SNP_ID_811404551 A-to-I Human chr11 - 13412662 13412662 13412662 AGAGTAGATAGTATTGTTTTGGGGAATTATTTATATCTTCCATAGTGCCCAGGATATCATCCTAC AGAGTAGATAGTATTGTTTTGGGGAATTATTTGTATCTTCCATAGTGCCCAGGATATCATCCTAC T C BTBD10 Ensembl:ENSG00000148925 Protein coding intron GSE100210 HepG2 cell line chr11:13412661..13412662 29129909 RNA-Seq:(High) rs1565240576 Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast HER-positive_carcinoma 4 breast RMVar_hsa_circ_28620,RMVar_hsa_circ_273865,RMVar_hsa_circ_276822,RMVar_hsa_circ_368178,RMVar_hsa_circ_269321,RMVar_hsa_circ_148312,RMVar_hsa_circ_148313,RMVar_hsa_circ_267339,RMVar_hsa_circ_314631,RMVar_hsa_circ_148314 54844 RMVar_ID_54844 Human_SNP_ID_811415480 A-to-I Human chr11 + 64188611 64188611 64188611 GTTTCCCAGGCTGGTCTCGAATTTCTAGGCTCAAGCAATCCTCTAGCCTTGGCCTCCCACTTCAT GTTTCCCAGGCTGGTCTCGAATTTCTAGGCTCGAGCAATCCTCTAGCCTTGGCCTCCCACTTCAT A G STIP1 Ensembl:ENSG00000168439 Protein coding intron GSE47997 K562 cells&HepG2 cells chr11:64188611..64188612 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - Human_RBP_ID_11666576 RMVar_hsa_circ_109104,RMVar_hsa_circ_150402 54845 RMVar_ID_54845 Human_SNP_ID_811511834 A-to-I Human chr11 + 33041628 33041628 33041628 CGAAAATTAGCGAGGCGTGGTGGTGGGCGCCTATAATCCCAGCTACTGGGGAGGCTGAGGCAGAA CGAAAATTAGCGAGGCGTGGTGGTGGGCGCCTGTAATCCCAGCTACTGGGGAGGCTGAGGCAGAA A G TCP11L1 Ensembl:ENSG00000176148 Protein coding intron GSE38233 cultured B-cells chr11:33041627..33041628 24183664 RNA-Seq:(High) rs4460781 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 4 large intestine GWAS_ID_5548,GWAS_ID_5549,GWAS_ID_5550,GWAS_ID_5551,GWAS_ID_5552,GWAS_ID_5553,GWAS_ID_5554,GWAS_ID_5555,GWAS_ID_5556,GWAS_ID_5557,GWAS_ID_5558,GWAS_ID_5559,GWAS_ID_5560,GWAS_ID_5561,GWAS_ID_5562,GWAS_ID_5563,GWAS_ID_5564,GWAS_ID_5565,GWAS_ID_5566,GWAS_ID_5567,GWAS_ID_5568,GWAS_ID_5569,GWAS_ID_5570,GWAS_ID_5571,GWAS_ID_5572,GWAS_ID_5573,GWAS_ID_5574,GWAS_ID_5575,GWAS_ID_5576,GWAS_ID_5577,GWAS_ID_5578,GWAS_ID_5579,GWAS_ID_5580,GWAS_ID_5581,GWAS_ID_5582,GWAS_ID_5583,GWAS_ID_5584,GWAS_ID_5585,GWAS_ID_5586,GWAS_ID_5587,GWAS_ID_5588,GWAS_ID_5589,GWAS_ID_5590,GWAS_ID_5591,GWAS_ID_5592,GWAS_ID_5593,GWAS_ID_5594,GWAS_ID_5595,GWAS_ID_5596,GWAS_ID_5597,GWAS_ID_5598,GWAS_ID_5599,GWAS_ID_5600,GWAS_ID_5601,GWAS_ID_5602,GWAS_ID_5603,GWAS_ID_5604,GWAS_ID_5605,GWAS_ID_5606,GWAS_ID_5607,GWAS_ID_5608,GWAS_ID_5609,GWAS_ID_5610,GWAS_ID_5611,GWAS_ID_5612,GWAS_ID_5613,GWAS_ID_5614,GWAS_ID_5615,GWAS_ID_5616,GWAS_ID_5617,GWAS_ID_5618,GWAS_ID_5619,GWAS_ID_5620,GWAS_ID_5621,GWAS_ID_5622,GWAS_ID_5623,GWAS_ID_5624,GWAS_ID_5625,GWAS_ID_5626,GWAS_ID_5627,GWAS_ID_5628,GWAS_ID_5629,GWAS_ID_5630,GWAS_ID_5631,GWAS_ID_5632,GWAS_ID_5633,GWAS_ID_5634,GWAS_ID_5635,GWAS_ID_5636,GWAS_ID_5637,GWAS_ID_5638,GWAS_ID_5639,GWAS_ID_5640,GWAS_ID_5641,GWAS_ID_5642,GWAS_ID_5643,GWAS_ID_5644,GWAS_ID_5645,GWAS_ID_5646,GWAS_ID_5647,GWAS_ID_5648,GWAS_ID_5649,GWAS_ID_5650,GWAS_ID_5651,GWAS_ID_5652,GWAS_ID_5653,GWAS_ID_5654,GWAS_ID_5655,GWAS_ID_5656,GWAS_ID_5657,GWAS_ID_5658,GWAS_ID_5659,GWAS_ID_5660,GWAS_ID_5661,GWAS_ID_5662,GWAS_ID_5663 54846 RMVar_ID_54846 Human_SNP_ID_811551542 A-to-I Human chr11 + 33161412 33161411 33161413 AAAATTAAACTAAAAACCACCCCCAAATCAGTAAAGTTACCCCCTGCCCAGCTGAGCCAGACCGC AAAATTAAACTAAAAACCACCCCCAAATCAGT__AGTTACCCCCTGCCCAGCTGAGCCAGACCGC TAA T - - Other Unknown GSE100210 HepG2 cell line chr11:33161411..33161412 29129909 RNA-Seq:(High) rs1408775438 Functional Loss DEL TCGA 33..34 33 COAD 1 - 54847 RMVar_ID_54847 Human_SNP_ID_811551542 A-to-I Human chr11 + 33161413 33161411 33161413 AAATTAAACTAAAAACCACCCCCAAATCAGTAAAGTTACCCCCTGCCCAGCTGAGCCAGACCGCC AAATTAAACTAAAAACCACCCCCAAATCAGT__AGTTACCCCCTGCCCAGCTGAGCCAGACCGCC TAA T - - Other Unknown GSE100210 HepG2 cell line chr11:33161413..33161414 29129909 RNA-Seq:(High) rs1408775438 Functional Loss DEL TCGA 32..33 33 COAD 1 - 54848 RMVar_ID_54848 Human_SNP_ID_811570582 A-to-I Human chr11 + 57684438 57684438 57684438 AAAACCCATCTCTACTAAAAATACAAAAAATTAGCCGGGTGTGGTGGCACATGCCTGTAATCCCA AAAACCCATCTCTACTAAAAATACAAAAAATTGGCCGGGTGTGGTGGCACATGCCTGTAATCCCA A G ZDHHC5 Ensembl:ENSG00000156599 Protein coding intron GSE38233 cultured B-cells chr11:57684437..57684438 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_2806,RMVar_hsa_circ_269514,RMVar_hsa_circ_73667,RMVar_hsa_circ_288914,RMVar_hsa_circ_312707,RMVar_hsa_circ_107222,RMVar_hsa_circ_149792,RMVar_hsa_circ_149793,RMVar_hsa_circ_149791 54849 RMVar_ID_54849 Human_SNP_ID_811601951 A-to-I Human chr11 - 72917123 72917123 72917123 AAAATTGGCTGGGCGTGGTGGTGGGTGCCTGTAGTCCCAGCTGCTTGGGAGGCTGAGGCAGGAGA AAAATTGGCTGGGCGTGGTGGTGGGTGCCTGTGGTCCCAGCTGCTTGGGAGGCTGAGGCAGGAGA T C FCHSD2 Ensembl:ENSG00000137478 Protein coding intron GSE100210 HepG2 cell line chr11:72917122..72917123 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_109945,RMVar_hsa_circ_151571,RMVar_hsa_circ_55803,RMVar_hsa_circ_151572,RMVar_hsa_circ_297389,RMVar_hsa_circ_24262,RMVar_hsa_circ_151579,RMVar_hsa_circ_319778,RMVar_hsa_circ_351999,RMVar_hsa_circ_30655,RMVar_hsa_circ_2597,RMVar_hsa_circ_70183,RMVar_hsa_circ_269727 54850 RMVar_ID_54850 Human_SNP_ID_811644192 A-to-I Human chr11 - 62625607 62625607 62625607 TGTGATCTCCTCACCTCTCCCACTCCATTGATACCAACTCTTTCCCTTCATTCCCCCAACATCCT TGTGATCTCCTCACCTCTCCCACTCCATTGATGCCAACTCTTTCCCTTCATTCCCCCAACATCCT T C GANAB Ensembl:ENSG00000089597 Protein coding 3'UTR GSE112787 293 Flip-In T-REx cells,empty vector chr11:62625606..62625607 29967493 RNA-Seq:(High) - Functional Loss SNV TCGA 33..33 33 LAML 1 - Human_RBP_ID_398947,Human_RBP_ID_17232578,Human_RBP_ID_17348916,Human_RBP_ID_17465311,Human_RBP_ID_17649614,Human_RBP_ID_17798163,Human_RBP_ID_18932452,Human_RBP_ID_19582332,Human_RBP_ID_24892434,Human_RBP_ID_26409591,Human_RBP_ID_26892667,Human_RBP_ID_27203368,Human_RBP_ID_27413055 54851 RMVar_ID_54851 Human_SNP_ID_811655950 A-to-I Human chr11 - 110265295 110265295 110265295 CTGAGGTCAGGAGTTTGAGACCAACCTGGCCAACATGGTGAAACCCCATCTCTACTAAAAATACA CTGAGGTCAGGAGTTTGAGACCAACCTGGCCAGCATGGTGAAACCCCATCTCTACTAAAAATACA T C RDX Ensembl:ENSG00000137710 Protein coding intron GSE38233 cultured B-cells chr11:110265294..110265295 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 9 breast RMVar_hsa_circ_358943,RMVar_hsa_circ_356221,RMVar_hsa_circ_355979,RMVar_hsa_circ_57247,RMVar_hsa_circ_366880,RMVar_hsa_circ_317062,RMVar_hsa_circ_332060 54852 RMVar_ID_54852 Human_SNP_ID_811659033 A-to-I Human chr11 + 64190171 64190171 64190171 TACAGGCATGCACCACCACATCCGGGCAATTTATTTATTTATTTATTTTTTTGAGACTGAGTTTC TACAGGCATGCACCACCACATCCGGGCAATTTTTTTATTTATTTATTTTTTTGAGACTGAGTTTC A T STIP1 Ensembl:ENSG00000168439 Protein coding intron GSE38233 cultured B-cells chr11:64190170..64190171 24183664 RNA-Seq:(High) rs1444146740 Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_109104,RMVar_hsa_circ_150402 54853 RMVar_ID_54853 Human_SNP_ID_811753982 A-to-I Human chr11 + 18665025 18665025 18665025 AGGCCCATCGGAGCATGTGGATTTGAGCCACCACATTTTTTAACCCTAGATCTCGAAATGCATCG AGGCCCATCGGAGCATGTGGATTTGAGCCACCGCATTTTTTAACCCTAGATCTCGAAATGCATCG A G - - Other Unknown GSE100210 HepG2 cell line chr11:18665024..18665025 29129909 RNA-Seq:(High) rs879228353 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_22790092,Human_RBP_ID_22896087,Human_RBP_ID_26402933,Human_RBP_ID_26888759,Human_RBP_ID_27410643 54854 RMVar_ID_54854 Human_SNP_ID_811789408 A-to-I Human chr11 + 74982268 74982268 74982268 CTACACCCCCAAAAGTGCCACAAGGTAGTCCTAGATGAATGCCTACACATGCAGACCCCAAGTTT CTACACCCCCAAAAGTGCCACAAGGTAGTCCTTGATGAATGCCTACACATGCAGACCCCAAGTTT A T lnc-SPCS2-1 RNACentral:URS00008BCC77 lincRNA intron GSE100210 HepG2 cell line chr11:74982267..74982268 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 54855 RMVar_ID_54855 Human_SNP_ID_811798247 A-to-I Human chr11 + 65441347 65441347 65441347 CTGAAAACTTTTATTTGTTTGTTTGTTTTAGTAGATGTGGGGTCTTTCTGTGTTGCCCGGACTGG CTGAAAACTTTTATTTGTTTGTTTGTTTTAGTGGATGTGGGGTCTTTCTGTGTTGCCCGGACTGG A G NEAT1 Ensembl:ENSG00000245532 lincRNA exon GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line chr11:65441346..65441347 29129909,31158229 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_752210,Human_RBP_ID_2275903,Human_RBP_ID_3378008,Human_RBP_ID_5093606,Human_RBP_ID_5169983,Human_RBP_ID_5246049,Human_RBP_ID_5549848,Human_RBP_ID_6085675,Human_RBP_ID_8247272,Human_RBP_ID_9005303,Human_RBP_ID_11673036,Human_RBP_ID_17108636,Human_RBP_ID_19700540,Human_RBP_ID_22791537,Human_RBP_ID_22892684,Human_RBP_ID_23154593,Human_RBP_ID_23514301,Human_RBP_ID_24461640,Human_RBP_ID_24896727,Human_RBP_ID_26894481 54856 RMVar_ID_54856 Human_SNP_ID_811806774 A-to-I Human chr11 - 62584986 62584986 62584986 GAAACCGTCTCTACTAAAAATACAAAAAAATTAGCTGGGCGTAGTGGCAGATTCCTGTAATCCCA GAAACCGTCTCTACTAAAAATACAAAAAAATTTGCTGGGCGTAGTGGCAGATTCCTGTAATCCCA T A AP002990.1,TUT1 Ensembl:ENSG00000255508,Ensembl:ENSG00000149016 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells chr11:62584985..62584986 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 5 breast RMVar_hsa_circ_55292,RMVar_hsa_circ_88200,RMVar_hsa_circ_150184,RMVar_hsa_circ_375054,RMVar_hsa_circ_150186,RMVar_hsa_circ_32168 54857 RMVar_ID_54857 Human_SNP_ID_811879180 A-to-I Human chr11 - 134379811 134379811 134379812 AGACCTCAGGGTGGAGTGAGCCCATGGTGGGCAGTGGGCAAGGCGGTGGGTGGTGGGCAAGGTGG AGACCTCAGGGTGGAGTGAGCCCATGGTGGGTGGTGGGCAAGGCGGTGGGTGGTGGGCAAGGTGG TG CA B3GAT1 Ensembl:ENSG00000109956 Protein coding exon GSE100210 HepG2 cell line chr11:134379810..134379811 29129909 RNA-Seq:(High) - Functional Loss MNV ICGC 32..33 33 MELA 1 - RMVar_hsa_circ_127943,RMVar_hsa_circ_154134 54858 RMVar_ID_54858 Human_SNP_ID_811890758 A-to-I Human chr11 - 66520831 66520831 66520831 CAGATGAGAAGATGAGGTGAGAGGACTGTTTGAGCCCAGGTGGCATAGGTTGCAGTAAGCTGAGA CAGATGAGAAGATGAGGTGAGAGGACTGTTTGCGCCCAGGTGGCATAGGTTGCAGTAAGCTGAGA T G ZDHHC24 Ensembl:ENSG00000174165 Protein coding 3'UTR GSE38233 cultured B-cells chr11:66520830..66520831 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 54859 RMVar_ID_54859 Human_SNP_ID_811892849 A-to-I Human chr11 + 65263345 65263345 65263345 AGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCGCCCGCCACCAGG AGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCGAGTAGCTGGGATTACAGGCGCCCGCCACCAGG A G AP000944.5,POLA2 Ensembl:ENSG00000285816,Ensembl:ENSG00000014138 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells chr11:65263344..65263345 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_24895199 RMVar_hsa_circ_85792,RMVar_hsa_circ_108397,RMVar_hsa_circ_96374,RMVar_hsa_circ_150604,RMVar_hsa_circ_150605,RMVar_hsa_circ_150603 54860 RMVar_ID_54860 Human_SNP_ID_811901334 A-to-I Human chr11 + 34085706 34085706 34085706 GGTGCCTGTAATCCCAGCTACCTGAGAGGCTGAGGCAGGAGAATTGCTTGAACCCGGGAGATGGA GGTGCCTGTAATCCCAGCTACCTGAGAGGCTGGGGCAGGAGAATTGCTTGAACCCGGGAGATGGA A G CAPRIN1 Ensembl:ENSG00000135387 Protein coding intron GSE100210 HepG2 cell line chr11:34085705..34085706 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_16986631 RMVar_hsa_circ_1867,RMVar_hsa_circ_91371,RMVar_hsa_circ_100857,RMVar_hsa_circ_126497,RMVar_hsa_circ_148986,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_148994,RMVar_hsa_circ_102755,RMVar_hsa_circ_332163,RMVar_hsa_circ_353773,RMVar_hsa_circ_357235,RMVar_hsa_circ_366718,RMVar_hsa_circ_343294,RMVar_hsa_circ_54105,RMVar_hsa_circ_149008,RMVar_hsa_circ_19666,RMVar_hsa_circ_113513,RMVar_hsa_circ_149000,RMVar_hsa_circ_86955,RMVar_hsa_circ_336186,RMVar_hsa_circ_84223,RMVar_hsa_circ_271765,RMVar_hsa_circ_149001,RMVar_hsa_circ_149002,RMVar_hsa_circ_290918,RMVar_hsa_circ_316383,RMVar_hsa_circ_306085,RMVar_hsa_circ_274498,RMVar_hsa_circ_106148,RMVar_hsa_circ_74569,RMVar_hsa_circ_149009,RMVar_hsa_circ_149006,RMVar_hsa_circ_149007,RMVar_hsa_circ_149005,RMVar_hsa_circ_41926,RMVar_hsa_circ_368120,RMVar_hsa_circ_281248,RMVar_hsa_circ_87599,RMVar_hsa_circ_149010,RMVar_hsa_circ_149011,RMVar_hsa_circ_348503,RMVar_hsa_circ_84718,RMVar_hsa_circ_149013,RMVar_hsa_circ_149014,RMVar_hsa_circ_149012 54861 RMVar_ID_54861 Human_SNP_ID_811902691 A-to-I Human chr11 - 59132795 59132795 59132795 AGATTGAGTAATTTATAAAGAAAAAGAGGTTTAATGTACTCACAGTTCCACATGGCAGAGGAGGC AGATTGAGTAATTTATAAAGAAAAAGAGGTTTGATGTACTCACAGTTCCACATGGCAGAGGAGGC T C FAM111A-DT Ensembl:ENSG00000245571 lincRNA intron GSE100210 HepG2 cell line chr11:59132794..59132795 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_5246149 54862 RMVar_ID_54862 Human_SNP_ID_811917807 A-to-I Human chr11 - 61813528 61813528 61813528 AGAGCACGGATTGGTGCATTTTACAAACCTCTAGCTACAGAAAAGTTCTCCAAGTCTGCACTCGA AGAGCACGGATTGGTGCATTTTACAAACCTCTCGCTACAGAAAAGTTCTCCAAGTCTGCACTCGA T G FADS1 Ensembl:ENSG00000149485 Protein coding intron GSE47997;GSE100210 K562 cells&HepG2 cells;HepG2 cell line chr11:61813527..61813528 23474544,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 5 liver Human_RBP_ID_17560324 Human_Splice_Rec_1246932,Human_Splice_Rec_1246954,Human_Splice_Rec_1246955,Human_Splice_Rec_1246958 54863 RMVar_ID_54863 Human_SNP_ID_811932970 A-to-I Human chr11 + 66756450 66756450 66756450 CACCTCCCAGGTTCAAGTGATTCTCATGCCTCAGTCCCCCGAGTAGCTGGGATTACAGATGCCCA CACCTCCCAGGTTCAAGTGATTCTCATGCCTCGGTCCCCCGAGTAGCTGGGATTACAGATGCCCA A G C11orf80 Ensembl:ENSG00000173715 Protein coding 5'UTR GSE107867 ASD brains,cerebellum chr11:66756449..66756450 30559470 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 bile_duct adenocarcinoma,biliary_tract adenocarcinoma 7 biliary tract,gallbladder Human_Splice_Rec_1264180,Human_Splice_Rec_1264181,Human_Splice_Rec_1264196,Human_Splice_Rec_1264197,Human_Splice_Rec_1264314,Human_Splice_Rec_1264315,Human_Splice_Rec_1264344,Human_Splice_Rec_1264345,Human_Splice_Rec_1264367 RMVar_hsa_circ_150946,RMVar_hsa_circ_72370,RMVar_hsa_circ_310218,RMVar_hsa_circ_317358,RMVar_hsa_circ_357601,RMVar_hsa_circ_321508,RMVar_hsa_circ_312564,RMVar_hsa_circ_294950,RMVar_hsa_circ_307988,RMVar_hsa_circ_279115,RMVar_hsa_circ_150948,RMVar_hsa_circ_150950,RMVar_hsa_circ_150951,RMVar_hsa_circ_150949,RMVar_hsa_circ_150947 54864 RMVar_ID_54864 Human_SNP_ID_811944024 A-to-I Human chr11 - 90282837 90282837 90282837 GGTTCCAAGTCTACAAACACAGCCCGGGGCACATGCTTGCCAGCACCCGTCTCACTGAAGGTGTT GGTTCCAAGTCTACAAACACAGCCCGGGGCACGTGCTTGCCAGCACCCGTCTCACTGAAGGTGTT T C - - Other Unknown GSE100210 HepG2 cell line chr11:90282836..90282837 29129909 RNA-Seq:(High) rs878985568 Functional Loss SNV ICGC 33..33 33 LAML 1 - 54865 RMVar_ID_54865 Human_SNP_ID_811950417 A-to-I Human chr11 + 91116017 91116017 91116017 ATTAAAGTCTTTTGATGACAAGCTTCAAAACTACAAAGAAGATGAACAGAGAAAGAAAATGGAAA ATTAAAGTCTTTTGATGACAAGCTTCAAAACTGCAAAGAAGATGAACAGAGAAAGAAAATGGAAA A G OSBPL9P3 Ensembl:ENSG00000255070 Pseudogene exon GSE100210 HepG2 cell line chr11:91116016..91116017 29129909 RNA-Seq:(High) rs1392461697 Functional Loss SNV ICGC 33..33 33 LAML 2 - 54866 RMVar_ID_54866 Human_SNP_ID_812000995 A-to-I Human chr11 - 67682754 67682754 67682754 TGCAGCATCCAGTTCATCTTAAGAATGTCAACAATTAGTCATGCAATAAATGTTCTGGTTTTAAA TGCAGCATCCAGTTCATCTTAAGAATGTCAACGATTAGTCATGCAATAAATGTTCTGGTTTTAAA T C - - Other Unknown GSE100210 HepG2 cell line chr11:67682753..67682754 29129909 RNA-Seq:(High) rs879110440 Functional Loss SNV ICGC 33..33 33 STAD 1 - Human_RBP_ID_26410684 54867 RMVar_ID_54867 Human_SNP_ID_812135754 A-to-I Human chr11 + 66806637 66806637 66806637 TAAAAATACAAAAATTAGCTGGACATGGTGGCACATGACTGTAGTCCCAGCTACTCGGGAGACTG TAAAAATACAAAAATTAGCTGGACATGGTGGCGCATGACTGTAGTCCCAGCTACTCGGGAGACTG A G C11orf80 Ensembl:ENSG00000173715 Protein coding intron GSE100210 HepG2 cell line chr11:66806636..66806637 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_24898832 RMVar_hsa_circ_150955,RMVar_hsa_circ_72370,RMVar_hsa_circ_357601,RMVar_hsa_circ_321508,RMVar_hsa_circ_307988,RMVar_hsa_circ_279115,RMVar_hsa_circ_150950,RMVar_hsa_circ_150951,RMVar_hsa_circ_336385,RMVar_hsa_circ_345505,RMVar_hsa_circ_320889,RMVar_hsa_circ_307201,RMVar_hsa_circ_28718,RMVar_hsa_circ_150956,RMVar_hsa_circ_150967,RMVar_hsa_circ_6520,RMVar_hsa_circ_150958,RMVar_hsa_circ_348252,RMVar_hsa_circ_350589,RMVar_hsa_circ_281728,RMVar_hsa_circ_18361,RMVar_hsa_circ_317313,RMVar_hsa_circ_378074,RMVar_hsa_circ_301715,RMVar_hsa_circ_13854,RMVar_hsa_circ_310484,RMVar_hsa_circ_150960,RMVar_hsa_circ_150962,RMVar_hsa_circ_150963,RMVar_hsa_circ_150961,RMVar_hsa_circ_337349,RMVar_hsa_circ_150964,RMVar_hsa_circ_340644,RMVar_hsa_circ_312212,RMVar_hsa_circ_150969,RMVar_hsa_circ_150970,RMVar_hsa_circ_150968,RMVar_hsa_circ_150973,RMVar_hsa_circ_277315,RMVar_hsa_circ_150965,RMVar_hsa_circ_150966,RMVar_hsa_circ_293208,RMVar_hsa_circ_297393,RMVar_hsa_circ_320353,RMVar_hsa_circ_291578,RMVar_hsa_circ_150975,RMVar_hsa_circ_150976,RMVar_hsa_circ_150974,RMVar_hsa_circ_150979,RMVar_hsa_circ_150971,RMVar_hsa_circ_150972,RMVar_hsa_circ_296045,RMVar_hsa_circ_308845,RMVar_hsa_circ_150977,RMVar_hsa_circ_150978 54868 RMVar_ID_54868 Human_SNP_ID_812187162 A-to-I Human chr11 + 90282631 90282631 90282631 ACGGTAACCGGGACCCAGTGTCTGCTCCTGTCACCTTCGCCTCCTAATCCCTAGCCACTATGCGT ACGGTAACCGGGACCCAGTGTCTGCTCCTGTCGCCTTCGCCTCCTAATCCCTAGCCACTATGCGT A G DISC1FP1,TUBAP2 Ensembl:ENSG00000261645,Ensembl:ENSG00000214391 lincRNA,Pseudogene intron,exon GSE100210 HepG2 cell line chr11:90282630..90282631 29129909 RNA-Seq:(High) rs879104709 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_4185329,Human_RBP_ID_8361185,Human_RBP_ID_26407803,Human_RBP_ID_27208141 Human_miRNA_ID_1893441 54869 RMVar_ID_54869 Human_SNP_ID_812194792 A-to-I Human chr11 - 134379811 134379811 134379811 AGACCTCAGGGTGGAGTGAGCCCATGGTGGGCAGTGGGCAAGGCGGTGGGTGGTGGGCAAGGTGG AGACCTCAGGGTGGAGTGAGCCCATGGTGGGCGGTGGGCAAGGCGGTGGGTGGTGGGCAAGGTGG T C B3GAT1 Ensembl:ENSG00000109956 Protein coding exon GSE100210 HepG2 cell line chr11:134379810..134379811 29129909 RNA-Seq:(High) rs903559680 Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_127943,RMVar_hsa_circ_154134 54870 RMVar_ID_54870 Human_SNP_ID_812203577 A-to-I Human chr11 + 62876807 62876807 62876807 TATTTTTAGTAGAAACGGGGTTTCACCATGTTAGCCAGGCTGATATTGAATTCCTGACCTCAATT TATTTTTAGTAGAAACGGGGTTTCACCATGTTGGCCAGGCTGATATTGAATTCCTGACCTCAATT A G SLC3A2 Ensembl:ENSG00000168003 Protein coding intron GSE38233;GSE56152;GSE100210 cultured B-cells;embryonic stem cells,wild type;HepG2 cell line chr11:62876806..62876807 24183664,25708366,29129909 RNA-Seq:(High) rs1431904822 Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 8 prostate Human_RBP_ID_11661079 Human_Splice_Rec_1250722,Human_Splice_Rec_1250723,Human_Splice_Rec_1250782,Human_Splice_Rec_1250783 RMVar_hsa_circ_150327,RMVar_hsa_circ_88690,RMVar_hsa_circ_126206,RMVar_hsa_circ_150331,RMVar_hsa_circ_79749,RMVar_hsa_circ_150330 54871 RMVar_ID_54871 Human_SNP_ID_812205608 A-to-I Human chr11 - 3756616 3756616 3756616 GGAGTTCGAGATAGACTGGCCAGCATGGTAAAACCCCATTTCTACTAAAAACACAAAAATTAGCT GGAGTTCGAGATAGACTGGCCAGCATGGTAAACCCCCATTTCTACTAAAAACACAAAAATTAGCT T G NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE100210 HepG2 cell line chr11:3756615..3756616 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - 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_97527,RMVar_hsa_circ_37210,RMVar_hsa_circ_38524,RMVar_hsa_circ_12367,RMVar_hsa_circ_147652,RMVar_hsa_circ_77589,RMVar_hsa_circ_106281,RMVar_hsa_circ_147654,RMVar_hsa_circ_147661,RMVar_hsa_circ_147658,RMVar_hsa_circ_109567,RMVar_hsa_circ_147659,RMVar_hsa_circ_125448,RMVar_hsa_circ_123681,RMVar_hsa_circ_147660,RMVar_hsa_circ_128055,RMVar_hsa_circ_126244,RMVar_hsa_circ_83167,RMVar_hsa_circ_50353,RMVar_hsa_circ_147670,RMVar_hsa_circ_147671,RMVar_hsa_circ_147669,RMVar_hsa_circ_106002,RMVar_hsa_circ_67070,RMVar_hsa_circ_68815,RMVar_hsa_circ_147680,RMVar_hsa_circ_373076,RMVar_hsa_circ_120713,RMVar_hsa_circ_147684,RMVar_hsa_circ_147685,RMVar_hsa_circ_85220,RMVar_hsa_circ_84143,RMVar_hsa_circ_121259,RMVar_hsa_circ_147686,RMVar_hsa_circ_101156,RMVar_hsa_circ_65040,RMVar_hsa_circ_92246,RMVar_hsa_circ_117554,RMVar_hsa_circ_147690,RMVar_hsa_circ_147691,RMVar_hsa_circ_147692,RMVar_hsa_circ_374371,RMVar_hsa_circ_147694,RMVar_hsa_circ_372984,RMVar_hsa_circ_147693,RMVar_hsa_circ_357330,RMVar_hsa_circ_97199,RMVar_hsa_circ_95967,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_147701,RMVar_hsa_circ_101460,RMVar_hsa_circ_301735,RMVar_hsa_circ_91945,RMVar_hsa_circ_147713,RMVar_hsa_circ_78263,RMVar_hsa_circ_147709,RMVar_hsa_circ_147708,RMVar_hsa_circ_333940,RMVar_hsa_circ_147712,RMVar_hsa_circ_348744,RMVar_hsa_circ_373682,RMVar_hsa_circ_346114,RMVar_hsa_circ_68884,RMVar_hsa_circ_114985,RMVar_hsa_circ_147714 54872 RMVar_ID_54872 Human_SNP_ID_812275562 A-to-I Human chr11 - 62642639 62642639 62642639 TCTAGGTCAGGAGTTCGATACGAGCCTGGCCAACATGATGAAACCCCGTCTCTACTAAAAATACA TCTAGGTCAGGAGTTCGATACGAGCCTGGCCAGCATGATGAAACCCCGTCTCTACTAAAAATACA T C GANAB Ensembl:ENSG00000089597 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells chr11:62642638..62642639 23474544,24183664 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 4 prostate 54873 RMVar_ID_54873 Human_SNP_ID_812277950 A-to-I Human chr11 + 62863093 62863068 62863093 ACAGGCGCTGCAACCACTCCCAGCTGATTTTTATGTTTTTAGTAGAGACGGGGTTTCACCATGTT ACAGGCGC_________________________TGTTTTTAGTAGAGACGGGGTTTCACCATGTT CTGCAACCACTCCCAGCTGATTTTTA C SLC3A2 Ensembl:ENSG00000168003 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr11:62863092..62863093 24183664,29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 9..33 33 PAAD 1 - RMVar_hsa_circ_98198,RMVar_hsa_circ_150327,RMVar_hsa_circ_88690,RMVar_hsa_circ_150326 54874 RMVar_ID_54874 Human_SNP_ID_812312661 A-to-I Human chr11 - 47762678 47762678 47762678 GAACTCCTGACTTCAAGTAATCCACCTGCCTCAGCCTCCCAAAGTGCTGGGATTAAACGCATGAG GAACTCCTGACTTCAAGTAATCCACCTGCCTCCGCCTCCCAAAGTGCTGGGATTAAACGCATGAG T G FNBP4 Ensembl:ENSG00000109920 Protein coding intron GSE38233 cultured B-cells chr11:47762677..47762678 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_104369,RMVar_hsa_circ_149625,RMVar_hsa_circ_360840,RMVar_hsa_circ_359423,RMVar_hsa_circ_90929,RMVar_hsa_circ_7244,RMVar_hsa_circ_149640,RMVar_hsa_circ_149647,RMVar_hsa_circ_149650,RMVar_hsa_circ_56304,RMVar_hsa_circ_268721 54875 RMVar_ID_54875 Human_SNP_ID_812356453 A-to-I Human chr11 - 3789632 3789632 3789632 ACATGCCTGTGGTCTCAGCTTTTTGGGAGGCTAAAGTGGGAGGATCAGTTGAACCCAGGAGGTCC ACATGCCTGTGGTCTCAGCTTTTTGGGAGGCTGAAGTGGGAGGATCAGTTGAACCCAGGAGGTCC T C NUP98 Ensembl:ENSG00000110713 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr11:3789631..3789632 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_125448,RMVar_hsa_circ_147660,RMVar_hsa_circ_128055,RMVar_hsa_circ_147669,RMVar_hsa_circ_92246,RMVar_hsa_circ_147707 54876 RMVar_ID_54876 Human_SNP_ID_812377698 A-to-I Human chr11 + 43898779 43898779 43898779 GTATTTCCTGTGCTCTGGACGCTGGTTAGTCCATTTATTGATGACAACACCAGAAGGAAATTCCT GTATTTCCTGTGCTCTGGACGCTGGTTAGTCCGTTTATTGATGACAACACCAGAAGGAAATTCCT A G ALKBH3,SEC14L1P1 Ensembl:ENSG00000166199,Ensembl:ENSG00000213693 Protein coding,Pseudogene intron,exon GSE100210 HepG2 cell line chr11:43898778..43898779 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue RMVar_hsa_circ_22093,RMVar_hsa_circ_48194,RMVar_hsa_circ_149254,RMVar_hsa_circ_93334,RMVar_hsa_circ_294653,RMVar_hsa_circ_95506,RMVar_hsa_circ_149257,RMVar_hsa_circ_75694,RMVar_hsa_circ_149259,RMVar_hsa_circ_149260,RMVar_hsa_circ_68460,RMVar_hsa_circ_357493 54877 RMVar_ID_54877 Human_SNP_ID_812394883 A-to-I Human chr11 + 73903596 73903596 73903596 AAAATGAGCTGGGTGTGGTGGCTGGAGCCTGTAATCCTAGCTACTTGGGAGTCTGAGGCAGGAGA AAAATGAGCTGGGTGTGGTGGCTGGAGCCTGTTATCCTAGCTACTTGGGAGTCTGAGGCAGGAGA A T PAAF1 Ensembl:ENSG00000175575 Protein coding intron GSE38233 cultured B-cells chr11:73903595..73903596 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_103792,RMVar_hsa_circ_348889,RMVar_hsa_circ_151644 54878 RMVar_ID_54878 Human_SNP_ID_812399961 A-to-I Human chr11 - 86010464 86010464 86010464 AAATTAGCCAGTCATGGAGGCGGGCACTTGTAATCCCAGCTACTTAGGAGGCTGAGGCAGGAGAA AAATTAGCCAGTCATGGAGGCGGGCACTTGTATTCCCAGCTACTTAGGAGGCTGAGGCAGGAGAA T A PICALM Ensembl:ENSG00000073921 Protein coding intron GSE38233 cultured B-cells chr11:86010463..86010464 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_152257,RMVar_hsa_circ_295279,RMVar_hsa_circ_272337,RMVar_hsa_circ_272743,RMVar_hsa_circ_119740,RMVar_hsa_circ_15803,RMVar_hsa_circ_7852,RMVar_hsa_circ_152238,RMVar_hsa_circ_152237,RMVar_hsa_circ_57042,RMVar_hsa_circ_342236,RMVar_hsa_circ_332531,RMVar_hsa_circ_322833,RMVar_hsa_circ_284486,RMVar_hsa_circ_152258,RMVar_hsa_circ_1706,RMVar_hsa_circ_32368,RMVar_hsa_circ_152269,RMVar_hsa_circ_7129,RMVar_hsa_circ_299460,RMVar_hsa_circ_114749,RMVar_hsa_circ_51418,RMVar_hsa_circ_100199,RMVar_hsa_circ_152268,RMVar_hsa_circ_152280,RMVar_hsa_circ_320251,RMVar_hsa_circ_152278,RMVar_hsa_circ_370213,RMVar_hsa_circ_274205,RMVar_hsa_circ_65207,RMVar_hsa_circ_303012,RMVar_hsa_circ_294372,RMVar_hsa_circ_64875,RMVar_hsa_circ_152288,RMVar_hsa_circ_279395,RMVar_hsa_circ_310150,RMVar_hsa_circ_329871,RMVar_hsa_circ_297237,RMVar_hsa_circ_279738,RMVar_hsa_circ_55198,RMVar_hsa_circ_152286,RMVar_hsa_circ_152287,RMVar_hsa_circ_339157,RMVar_hsa_circ_121530,RMVar_hsa_circ_273929,RMVar_hsa_circ_85100,RMVar_hsa_circ_152295,RMVar_hsa_circ_370518,RMVar_hsa_circ_152290,RMVar_hsa_circ_152289,RMVar_hsa_circ_304884,RMVar_hsa_circ_360237,RMVar_hsa_circ_152296,RMVar_hsa_circ_298649,RMVar_hsa_circ_346370,RMVar_hsa_circ_374123,RMVar_hsa_circ_302447,RMVar_hsa_circ_273802,RMVar_hsa_circ_19046,RMVar_hsa_circ_152298,RMVar_hsa_circ_152299,RMVar_hsa_circ_288067,RMVar_hsa_circ_152297,RMVar_hsa_circ_337054,RMVar_hsa_circ_272959,RMVar_hsa_circ_152300 54879 RMVar_ID_54879 Human_SNP_ID_812444199 A-to-I Human chr11 + 62857543 62857543 62857543 TACCGATCTCTACAAAAAAAATAGAAAAAATTAGCCAGGAGCGGTGGTGCATGCCTGTAGCCCCA TACCGATCTCTACAAAAAAAATAGAAAAAATTTGCCAGGAGCGGTGGTGCATGCCTGTAGCCCCA A T SLC3A2 Ensembl:ENSG00000168003 Protein coding intron GSE100210 HepG2 cell line chr11:62857542..62857543 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - RMVar_hsa_circ_98198,RMVar_hsa_circ_150327,RMVar_hsa_circ_88690,RMVar_hsa_circ_150326 54880 RMVar_ID_54880 Human_SNP_ID_812544881 A-to-I Human chr11 + 119006634 119006634 119006634 CTCGTGATCCACCCGCCTCGGCCTCCCAAAGTACTGGGATTACAGGCGTGAGCCACTGCGCCTGG CTCGTGATCCACCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGCGCCTGG A G CCDC84 Ensembl:ENSG00000186166 Protein coding intron GSE47997;GSE38233;GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829;GSE126723:GSM3611833,GSM3611834,GSM3611835 K562 cells&HepG2 cells;cultured B-cells;HepG2 cell line;Bronchiolar epithelium,BEP2D cell line;Bronchiolar epithelium,BERP35T4 cell line chr11:119006633..119006634 23474544,24183664,29129909,31158229,31158229 RNA-Seq:(High) rs1013674606 Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 1 prostate RMVar_hsa_circ_109102,RMVar_hsa_circ_153446 54881 RMVar_ID_54881 Human_SNP_ID_812568389 A-to-I Human chr11 + 43866403 43866403 43866403 AGGAGGTCGAGACTGCAGTGAGTTGTGATTGCACCACAGCACTCCAGCCTGGGTGACAGAGTGAG AGGAGGTCGAGACTGCAGTGAGTTGTGATTGCGCCACAGCACTCCAGCCTGGGTGACAGAGTGAG A G - - Other Unknown GSE100210 HepG2 cell line chr11:43866402..43866403 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 54882 RMVar_ID_54882 Human_SNP_ID_812599720 A-to-I Human chr11 - 65371771 65371771 65371771 TCTCTACTAAAAATACAAAAAATTAGCCGGGCATGGTGGCACGCACCTGTAGTCACAGTTACTTG TCTCTACTAAAAATACAAAAAATTAGCCGGGCGTGGTGGCACGCACCTGTAGTCACAGTTACTTG T C L13304-001,L13705-009 RNACentral:URS000044B5AA,RNACentral:URS00001E2917 scRNA,misc_RNA intron,intron GSE38233 cultured B-cells chr11:65371770..65371771 24183664 RNA-Seq:(High) rs551233005 Functional Loss SNV ICGC 33..33 33 ESCA 1 - 54883 RMVar_ID_54883 Human_SNP_ID_812633916 A-to-I Human chr11 - 8655617 8655617 8655617 CACCACGCCTGACTAATTTTTGTATTTTTAGTAGATACTGGGTTTTTCTATGTTGACCAAGCTGG CACCACGCCTGACTAATTTTTGTATTTTTAGTGGATACTGGGTTTTTCTATGTTGACCAAGCTGG T C TRIM66 Ensembl:ENSG00000166436 Protein coding intron GSE100210 HepG2 cell line chr11:8655616..8655617 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 54884 RMVar_ID_54884 Human_SNP_ID_812634495 A-to-I Human chr11 - 122960393 122960393 122960393 GGTCCTTGTTGCCTGCAATACCCCTGGACCTAAGAAAACTGCATTCTACAGAGAGGGGGCCACTG GGTCCTTGTTGCCTGCAATACCCCTGGACCTAGGAAAACTGCATTCTACAGAGAGGGGGCCACTG T C - - Other Unknown GSE100210 HepG2 cell line chr11:122960392..122960393 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 54885 RMVar_ID_54885 Human_SNP_ID_812641070 A-to-I Human chr11 - 90283044 90283044 90283044 AAGCTGTGGAAAACCAAGAAGCCCTGAAAACCAGTGCACTGGTTAGCCAGCTTGCGAATTCGGTC AAGCTGTGGAAAACCAAGAAGCCCTGAAAACCGGTGCACTGGTTAGCCAGCTTGCGAATTCGGTC T C - - Other Unknown GSE100210 HepG2 cell line chr11:90283043..90283044 29129909 RNA-Seq:(High) rs879176955 Functional Loss SNV ICGC 33..33 33 LAML 2 - 54886 RMVar_ID_54886 Human_SNP_ID_812649330 A-to-I Human chr11 + 90282615 90282615 90282615 TCTTAGCTTGTTGGGGACGGTAACCGGGACCCAGTGTCTGCTCCTGTCACCTTCGCCTCCTAATC TCTTAGCTTGTTGGGGACGGTAACCGGGACCCGGTGTCTGCTCCTGTCACCTTCGCCTCCTAATC A G DISC1FP1,TUBAP2 Ensembl:ENSG00000261645,Ensembl:ENSG00000214391 lincRNA,Pseudogene intron,exon GSE100210 HepG2 cell line chr11:90282614..90282615 29129909 RNA-Seq:(High) rs878893494 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_8361185,Human_RBP_ID_27208141 Human_miRNA_ID_1893441 54887 RMVar_ID_54887 Human_SNP_ID_812684653 A-to-I Human chr11 - 91114818 91114818 91114818 AGAACCCCAAGAAAGGAAAGAGGGAAAGAGAAAGAAATTCAGTGGGAGACAAGGTTATTTCATAA AGAACCCCAAGAAAGGAAAGAGGGAAAGAGAAGGAAATTCAGTGGGAGACAAGGTTATTTCATAA T C OSBPL9P2 Ensembl:ENSG00000254677 Pseudogene exon GSE100210 HepG2 cell line chr11:91114817..91114818 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 STAD 1 - 54888 RMVar_ID_54888 Human_SNP_ID_812706265 A-to-I Human chr11 - 6614962 6614962 6614962 TAGGCCTCTACTCCAGTGTTTGGGGGGATCCTATCCTTGATCAATGAGCACAGGATCCTTAGTGG TAGGCCTCTACTCCAGTGTTTGGGGGGATCCTTTCCTTGATCAATGAGCACAGGATCCTTAGTGG T A TPP1,AC091564.7 Ensembl:ENSG00000166340,Ensembl:ENSG00000285338 Protein coding,lincRNA CDS,exon GSE112787 293 Flip-In T-REx cells,empty vector chr11:6614961..6614962 29967493 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,large_intestine adenocarcinoma 8 large intestine Human_RBP_ID_5093547,Human_RBP_ID_22753339 Human_Splice_Rec_1205220,Human_Splice_Rec_1205221,Human_Splice_Rec_1205250,Human_Splice_Rec_1205251,Human_Splice_Rec_1205272,Human_Splice_Rec_1205273,Human_Splice_Rec_1205276,Human_Splice_Rec_1205294,Human_Splice_Rec_1205295,Human_Splice_Rec_1205316,Human_Splice_Rec_1205317,Human_Splice_Rec_1205336,Human_Splice_Rec_1205337,Human_Splice_Rec_1205356,Human_Splice_Rec_1205357,Human_Splice_Rec_1205378,Human_Splice_Rec_1205379,Human_Splice_Rec_1205400,Human_Splice_Rec_1205401,Human_Splice_Rec_1205414,Human_Splice_Rec_1205415,Human_Splice_Rec_1205436,Human_Splice_Rec_1205437,Human_Splice_Rec_1205458,Human_Splice_Rec_1205459,Human_Splice_Rec_1205478,Human_Splice_Rec_1205479,Human_Splice_Rec_1205494,Human_Splice_Rec_1205495,Human_Splice_Rec_1205498,Human_Splice_Rec_1205499,Human_Splice_Rec_1205520,Human_Splice_Rec_1205521,Human_Splice_Rec_1205544,Human_Splice_Rec_1205545,Human_Splice_Rec_1205568,Human_Splice_Rec_1205569,Human_Splice_Rec_1205584,Human_Splice_Rec_1205585,Human_Splice_Rec_1205606,Human_Splice_Rec_1205607,Human_Splice_Rec_1205630,Human_Splice_Rec_1205631,Human_Splice_Rec_1205640,Human_Splice_Rec_1205641,Human_Splice_Rec_1205648,Human_Splice_Rec_1205649 RMVar_hsa_circ_104886,RMVar_hsa_circ_127882,RMVar_hsa_circ_88580,RMVar_hsa_circ_147886,RMVar_hsa_circ_97872,RMVar_hsa_circ_147887,RMVar_hsa_circ_147885,RMVar_hsa_circ_147888 54889 RMVar_ID_54889 Human_SNP_ID_812731208 A-to-I Human chr11 + 43866184 43866184 43866184 GACTATGAAAGGGGCCAGACTCTGTGGCTCACACCTGTAACCCCAGCACTTTGGGAGGCTGAGGT GACTATGAAAGGGGCCAGACTCTGTGGCTCACGCCTGTAACCCCAGCACTTTGGGAGGCTGAGGT A G - - Other Unknown GSE100210 HepG2 cell line chr11:43866183..43866184 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 54890 RMVar_ID_54890 Human_SNP_ID_812746601 A-to-I Human chr11 + 91116059 91116059 91116059 TGAACAGAGAAAGAAAATGGAAACTCTCAAAGAAACAACAAATAGCATAGTAGAATCAGCTAAAC TGAACAGAGAAAGAAAATGGAAACTCTCAAAGGAACAACAAATAGCATAGTAGAATCAGCTAAAC A G OSBPL9P3 Ensembl:ENSG00000255070 Pseudogene exon GSE100210 HepG2 cell line chr11:91116059..91116060 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - 54891 RMVar_ID_54891 Human_SNP_ID_812829853 A-to-I Human chr11 - 86195888 86195888 86195888 AGTGTATTGGACTTCTCTCTCCAATACAGCACAATCATTGTAGCCAGTGGTGTTGGAAATAACAA AGTGTATTGGACTTCTCTCTCCAATACAGCACGATCATTGTAGCCAGTGGTGTTGGAAATAACAA T C - - Other Unknown GSE100210 HepG2 cell line chr11:86195887..86195888 29129909 RNA-Seq:(High) rs907562285 Functional Loss SNV ICGC 33..33 33 LAML 2 - 54892 RMVar_ID_54892 Human_SNP_ID_812839297 A-to-I Human chr11 + 32906614 32906614 32906614 GTTTTTGTTCATTGTAGAGATGGGGTCTTGCTATTTTCTCAGGGTGGTCTCAAACTTCTGGGCTC GTTTTTGTTCATTGTAGAGATGGGGTCTTGCTGTTTTCTCAGGGTGGTCTCAAACTTCTGGGCTC A G QSER1 Ensembl:ENSG00000060749 Protein coding intron GSE100210 HepG2 cell line chr11:32906613..32906614 29129909 RNA-Seq:(High) rs961450158 Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 2 breast 54893 RMVar_ID_54893 Human_SNP_ID_812898002 A-to-I Human chr11 + 1232750 1232750 1232750 CGCCTGTGCCGCCAAGGGCGTACAGCTCAGCGACTGGAGGGACGGCGTCTGCAGTGAGTGCCCAC CGCCTGTGCCGCCAAGGGCGTACAGCTCAGCGGCTGGAGGGACGGCGTCTGCAGTGAGTGCCCAC A G MUC5B Ensembl:ENSG00000117983 Protein coding exon GSE47997 K562 cells&HepG2 cells chr11:1232749..1232750 23474544 RNA-Seq:(High) rs202127660 Functional Loss SNV ICGC,COSMIC 33..33 33 central_nervous_system astrocytoma_Grade_IV,colon adenocarcinoma,lung adenocarcinoma,brain astrocytoma_Grade_IV,liver neoplasm,lung non_small_cell_carcinoma,liver hepatocellular_carcinoma,thyroid neoplasm,THCA,head_neck squamous_cell_carcinoma,lung large_cell_carcinoma,large_intestine adenocarcinoma,pharynx nasopharyngeal_carcinoma 35 lung,liver,head and neck,large intestine,brain Human_Splice_Rec_1197137,Human_Splice_Rec_1197185 54894 RMVar_ID_54894 Human_SNP_ID_812934462 A-to-I Human chr11 + 63819368 63819368 63819368 TAGTAGCTGGGATTACAGGCGTGCGCCACCATACCCGGCTAATTTTTGTATTTTTAGTAGAGACA TAGTAGCTGGGATTACAGGCGTGCGCCACCATGCCCGGCTAATTTTTGTATTTTTAGTAGAGACA A G SPINDOC Ensembl:ENSG00000168005 Protein coding intron GSE38233 cultured B-cells chr11:63819367..63819368 24183664 RNA-Seq:(High) rs1235127145 Functional Loss SNV ICGC 33..33 33 ESCA 2 - RMVar_hsa_circ_78377,RMVar_hsa_circ_150371,RMVar_hsa_circ_97315,RMVar_hsa_circ_150372,RMVar_hsa_circ_150378,RMVar_hsa_circ_101809 54895 RMVar_ID_54895 Human_SNP_ID_812946464 A-to-I Human chr11 - 27890774 27890774 27890774 GCATATTAACCTTATACCAAACAAACAAGATCAAACTCTCACTATTGTGGATACTGGAATTGGAA GCATATTAACCTTATACCAAACAAACAAGATCGAACTCTCACTATTGTGGATACTGGAATTGGAA T C HSP90AA2P Ensembl:ENSG00000224411 Pseudogene exon GSE100210 HepG2 cell line chr11:27890773..27890774 29129909 RNA-Seq:(High) rs1215276056 Functional Loss SNV ICGC 33..33 33 LAML 2 - 54896 RMVar_ID_54896 Human_SNP_ID_812954825 A-to-I Human chr11 + 97340329 97340329 97340329 TCACTGCAGGCTCTGCCTCCCAGGTTCACGCCATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGA TCACTGCAGGCTCTGCCTCCCAGGTTCACGCCGTTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGA A G - - Other Unknown GSE100210 HepG2 cell line chr11:97340328..97340329 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - 54897 RMVar_ID_54897 Human_SNP_ID_812958051 A-to-I Human chr11 - 10805911 10805911 10805911 AAGAACGACATGATGCAATCTTCAGGAAAGTAAGAGGGTAAGTTTCAAGGTCTGTTTTACTAAAA AAGAACGACATGATGCAATCTTCAGGAAAGTAGGAGGGTAAGTTTCAAGGTCTGTTTTACTAAAA T C EIF4G2 Ensembl:ENSG00000110321 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector chr11:10805910..10805911 29967493 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 lung adenocarcinoma 5 lung Human_RBP_ID_1453901,Human_RBP_ID_1775170,Human_RBP_ID_8344107,Human_RBP_ID_8766530,Human_RBP_ID_9343911,Human_RBP_ID_11516762,Human_RBP_ID_23113062,Human_RBP_ID_23485072 Human_Splice_Rec_1210501,Human_Splice_Rec_1210541,Human_Splice_Rec_1210577,Human_Splice_Rec_1210611,Human_Splice_Rec_1210653,Human_Splice_Rec_1210727,Human_Splice_Rec_1210751,Human_Splice_Rec_1210761,Human_Splice_Rec_1210787,Human_Splice_Rec_1210799,Human_Splice_Rec_1210803,Human_Splice_Rec_1210810,Human_Splice_Rec_1210811,Human_Splice_Rec_1210819,Human_Splice_Rec_1210827,Human_Splice_Rec_1210834,Human_Splice_Rec_1210835,Human_Splice_Rec_1210847,Human_Splice_Rec_1210857,Human_Splice_Rec_1210863,Human_Splice_Rec_1210869,Human_Splice_Rec_1210875 RMVar_hsa_circ_6954,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_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_148215,RMVar_hsa_circ_148216,RMVar_hsa_circ_280734,RMVar_hsa_circ_22870,RMVar_hsa_circ_148219,RMVar_hsa_circ_148221,RMVar_hsa_circ_366770,RMVar_hsa_circ_47593,RMVar_hsa_circ_52449,RMVar_hsa_circ_22468 54898 RMVar_ID_54898 Human_SNP_ID_813064944 A-to-I Human chr11 - 96327839 96327839 96327839 CGCCTGCCTTGGCTTCCCAAAGTGCTGGGATTACAGGTGTGAGGCATCGTGTCTGGCCTGATTAT CGCCTGCCTTGGCTTCCCAAAGTGCTGGGATTGCAGGTGTGAGGCATCGTGTCTGGCCTGATTAT T C MAML2 Ensembl:ENSG00000184384 Protein coding intron GSE107867 ASD brains,cerebellum chr11:96327838..96327839 30559470 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 1 prostate RMVar_hsa_circ_101444,RMVar_hsa_circ_152610 54899 RMVar_ID_54899 Human_SNP_ID_813081729 A-to-I Human chr11 - 90282872 90282872 90282872 GGTAGGTGCCAGTGCAAACTTCATCAATGACCATGGGTTCCAAGTCTACAAACACAGCCCGGGGC GGTAGGTGCCAGTGCAAACTTCATCAATGACCGTGGGTTCCAAGTCTACAAACACAGCCCGGGGC T C - - Other Unknown GSE100210 HepG2 cell line chr11:90282871..90282872 29129909 RNA-Seq:(High) rs879245602 Functional Loss SNV ICGC 33..33 33 LAML 2 - 54900 RMVar_ID_54900 Human_SNP_ID_813184410 A-to-I Human chr11 + 3817800 3817800 3817800 CGGGCGCAGTGGCTCATACCTGTAATCTCAGCACCTCGGGAGGGCGAAGCCAGTGGATCACTCGA CGGGCGCAGTGGCTCATACCTGTAATCTCAGCGCCTCGGGAGGGCGAAGCCAGTGGATCACTCGA A G PGAP2 Ensembl:ENSG00000148985 Protein coding intron GSE100210 HepG2 cell line chr11:3817799..3817800 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 bile_duct adenocarcinoma,biliary_tract adenocarcinoma 17 biliary tract,gallbladder Human_RBP_ID_1264538 54901 RMVar_ID_54901 Human_SNP_ID_813191386 A-to-I Human chr11 - 33161339 33161339 33161339 AGCTTCCCATCGACGGTCAGTGCGCACGTTGTAATCAGCTGAGGCCATGTCAGGAGACGGAGCCA AGCTTCCCATCGACGGTCAGTGCGCACGTTGTTATCAGCTGAGGCCATGTCAGGAGACGGAGCCA T A CSTF3 Ensembl:ENSG00000176102 Protein coding 5'UTR GSE100210 HepG2 cell line chr11:33161338..33161339 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 6 lung Human_RBP_ID_31644,Human_RBP_ID_807608,Human_RBP_ID_869426,Human_RBP_ID_4189970,Human_RBP_ID_5436400,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_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 54902 RMVar_ID_54902 Human_SNP_ID_813194257 A-to-I Human chr11 + 18406717 18406717 18406717 CAGCCTGGGCAACAAGAGTGAAACTCCATCTCAAAAGAAAAAAAAAAGCGGCTGGGCTCTGTGGC CAGCCTGGGCAACAAGAGTGAAACTCCATCTCGAAAGAAAAAAAAAAGCGGCTGGGCTCTGTGGC A G AC084117.1,LDHA Ensembl:ENSG00000256006,Ensembl:ENSG00000134333 lincRNA,Protein coding exon,intron GSE38233 cultured B-cells chr11:18406716..18406717 24183664 RNA-Seq:(High) rs10832933 Functional Loss SNV ICGC 33..33 33 SKCA 1 - Human_RBP_ID_6111796 Human_Splice_Rec_1218936 RMVar_hsa_circ_106856,RMVar_hsa_circ_148596 54903 RMVar_ID_54903 Human_SNP_ID_813213730 A-to-I Human chr11 - 9299703 9299703 9299703 ATTTATCTTAATTATACTTTCTTTTTTCTTCCAGAAAAATCCTGGGTAGAAGCTGGATCAGCAAG ATTTATCTTAATTATACTTTCTTTTTTCTTCCGGAAAAATCCTGGGTAGAAGCTGGATCAGCAAG T C TMEM41B Ensembl:ENSG00000166471 Protein coding intron GSE105773 Glioblastoma cells,U87MG chr11:9299702..9299703 29724793 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 8 large intestine Human_RBP_ID_22640925,Human_RBP_ID_24912120 54904 RMVar_ID_54904 Human_SNP_ID_813214703 A-to-I Human chr11 - 40248594 40248594 40248594 GGCTCAGGTGATCCTCCTGCTTCAGAATCCCAAGTTGCTGGGACTACGGGGTCATACCACCATGC GGCTCAGGTGATCCTCCTGCTTCAGAATCCCACGTTGCTGGGACTACGGGGTCATACCACCATGC T G LRRC4C Ensembl:ENSG00000148948 Protein coding intron GSE107867 ASD brains,frontal_cortex chr11:40248593..40248594 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 3 - RMVar_hsa_circ_7529,RMVar_hsa_circ_39906,RMVar_hsa_circ_42641 54905 RMVar_ID_54905 Human_SNP_ID_813242056 A-to-I Human chr11 - 43898152 43898152 43898152 GTCAAATCGCCCAGGTATCTCTTGATGTAGTCAGCATCTAGTTTGTTATCAGGGATGCCCACCAC GTCAAATCGCCCAGGTATCTCTTGATGTAGTCGGCATCTAGTTTGTTATCAGGGATGCCCACCAC T C - - Other Unknown GSE100210 HepG2 cell line chr11:43898151..43898152 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue 54906 RMVar_ID_54906 Human_SNP_ID_813280596 A-to-I Human chr11 - 95859550 95859516 95859551 TGCATTTAAAGAATGTCGGTAGATAAGAACATAGGAAAAGTCTACAATACCAATTTTTCCCCACC TGCATTTAAAGAATGTCGGTAGATAAGAACA__________________________________ GTGGTGGGGAAAAATTGGTATTGTAGACTTTTCCTA G MTMR2 Ensembl:ENSG00000087053 Protein coding intron GSE100210 HepG2 cell line chr11:95859549..95859550 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 32..65 33 OV 1 - RMVar_hsa_circ_152589,RMVar_hsa_circ_92720,RMVar_hsa_circ_90492,RMVar_hsa_circ_266630,RMVar_hsa_circ_49882,RMVar_hsa_circ_53657,RMVar_hsa_circ_101748,RMVar_hsa_circ_84825,RMVar_hsa_circ_152598,RMVar_hsa_circ_152599,RMVar_hsa_circ_152597,RMVar_hsa_circ_324655,RMVar_hsa_circ_363270,RMVar_hsa_circ_54072,RMVar_hsa_circ_33640,RMVar_hsa_circ_152601,RMVar_hsa_circ_50933,RMVar_hsa_circ_21439 54907 RMVar_ID_54907 Human_SNP_ID_813301521 A-to-I Human chr11 + 66776268 66776268 66776268 TTTAGTAGAGATGGGATTCTACCATGTTGGCCAGCCTGGTCTTGAACTCCTGACCTCAAGTGATC TTTAGTAGAGATGGGATTCTACCATGTTGGCCGGCCTGGTCTTGAACTCCTGACCTCAAGTGATC A G C11orf80 Ensembl:ENSG00000173715 Protein coding intron GSE100210 HepG2 cell line chr11:66776267..66776268 29129909 RNA-Seq:(High) rs1167724180 Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 8 oesophagus RMVar_hsa_circ_150955,RMVar_hsa_circ_72370,RMVar_hsa_circ_310218,RMVar_hsa_circ_317358,RMVar_hsa_circ_357601,RMVar_hsa_circ_321508,RMVar_hsa_circ_294950,RMVar_hsa_circ_307988,RMVar_hsa_circ_279115,RMVar_hsa_circ_150948,RMVar_hsa_circ_150950,RMVar_hsa_circ_150951,RMVar_hsa_circ_150949,RMVar_hsa_circ_336385,RMVar_hsa_circ_345505,RMVar_hsa_circ_377429,RMVar_hsa_circ_344408,RMVar_hsa_circ_309700,RMVar_hsa_circ_320889,RMVar_hsa_circ_307201,RMVar_hsa_circ_17767,RMVar_hsa_circ_28718,RMVar_hsa_circ_150956,RMVar_hsa_circ_327709 54908 RMVar_ID_54908 Human_SNP_ID_813371682 A-to-I Human chr11 + 65439533 65439533 65439533 CATAGCGAAAACTTGTCTCTACTAAAAATACAAAAATTAGTCAGGCATGGTGGTGCACGTCTGTA CATAGCGAAAACTTGTCTCTACTAAAAATACAGAAATTAGTCAGGCATGGTGGTGCACGTCTGTA A G NEAT1 Ensembl:ENSG00000245532 lincRNA exon GSE100210 HepG2 cell line chr11:65439533..65439534 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_2295803,Human_RBP_ID_3389382,Human_RBP_ID_9005287,Human_RBP_ID_9655897,Human_RBP_ID_17108617,Human_RBP_ID_17184617,Human_RBP_ID_19700533,Human_RBP_ID_22381136,Human_RBP_ID_22892614,Human_RBP_ID_23154563,Human_RBP_ID_23514239,Human_RBP_ID_24917918,Human_RBP_ID_27204866 54909 RMVar_ID_54909 Human_SNP_ID_813379398 A-to-I Human chr11 + 65269294 65269294 65269294 CACGAGGTCAGGAGATCGAGACCATCCTGGTTAACATGGTGAAACTCTGTCTCTACCATAAATAC CACGAGGTCAGGAGATCGAGACCATCCTGGTTGACATGGTGAAACTCTGTCTCTACCATAAATAC A G AP000944.5,POLA2 Ensembl:ENSG00000285816,Ensembl:ENSG00000014138 Protein coding,Protein coding intron,intron GSE38233 cultured B-cells chr11:65269293..65269294 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 STAD 1 - RMVar_hsa_circ_25259,RMVar_hsa_circ_85792,RMVar_hsa_circ_96374,RMVar_hsa_circ_150604,RMVar_hsa_circ_150603,RMVar_hsa_circ_61956,RMVar_hsa_circ_341351 54910 RMVar_ID_54910 Human_SNP_ID_813412230 A-to-I Human chr11 - 47170707 47170707 47170707 TCCTGGGTTTAAGTACCTTGGCTTCACAAAGTACTGGGATTACAGATGTGAGCCACCATGTCTGG TCCTGGGTTTAAGTACCTTGGCTTCACAAAGTGCTGGGATTACAGATGTGAGCCACCATGTCTGG T C ARFGAP2 Ensembl:ENSG00000149182 Protein coding intron GSE100210 HepG2 cell line chr11:47170706..47170707 29129909 RNA-Seq:(High) rs754235613 Functional Loss SNV ICGC 33..33 33 MALY 1 - Human_RBP_ID_1264725 RMVar_hsa_circ_101647,RMVar_hsa_circ_34157,RMVar_hsa_circ_74477,RMVar_hsa_circ_84663,RMVar_hsa_circ_149483,RMVar_hsa_circ_149484 54911 RMVar_ID_54911 Human_SNP_ID_813423587 A-to-I Human chr11 - 62823303 62823303 62823303 GGACATGGTTGCGTGTGCCTGTGGTTCCAGCTACTCGGGAGGCTGAGGCGGGAGGATGACTTAAG GGACATGGTTGCGTGTGCCTGTGGTTCCAGCTGCTCGGGAGGCTGAGGCGGGAGGATGACTTAAG T C STX5 Ensembl:ENSG00000162236 Protein coding intron GSE100210 HepG2 cell line chr11:62823302..62823303 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - RMVar_hsa_circ_150281,RMVar_hsa_circ_82797,RMVar_hsa_circ_91054,RMVar_hsa_circ_150282 54912 RMVar_ID_54912 Human_SNP_ID_813474580 A-to-I Human chr11 + 64188651 64188651 64188651 CTCTAGCCTTGGCCTCCCACTTCATTAGCACTAGGATTACAGGCGTGAGTCACCTTGCCTGGTCT CTCTAGCCTTGGCCTCCCACTTCATTAGCACTGGGATTACAGGCGTGAGTCACCTTGCCTGGTCT A G STIP1 Ensembl:ENSG00000168439 Protein coding intron GSE38233 cultured B-cells chr11:64188650..64188651 24183664 RNA-Seq:(High) rs1162648312 Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_11666577 RMVar_hsa_circ_109104,RMVar_hsa_circ_150402 54913 RMVar_ID_54913 Human_SNP_ID_813496470 A-to-I Human chr11 - 43898130 43898130 43898130 TGATGTAGTCAGCATCTAGTTTGTTATCAGGGATGCCCACCACGGGCTCAGGTGCACTGGGGCTG TGATGTAGTCAGCATCTAGTTTGTTATCAGGGGTGCCCACCACGGGCTCAGGTGCACTGGGGCTG T C - - Other Unknown GSE100210 HepG2 cell line chr11:43898129..43898130 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue 54914 RMVar_ID_54914 Human_SNP_ID_813520577 A-to-I Human chr11 + 64190064 64190064 64190064 ACTCTGTCCTCCAGGTGAGAATGCAGTGGTGCAATCTCGGCTCACTGCAGCCTCCGACTCCCAGG ACTCTGTCCTCCAGGTGAGAATGCAGTGGTGCGATCTCGGCTCACTGCAGCCTCCGACTCCCAGG A G STIP1 Ensembl:ENSG00000168439 Protein coding intron GSE38233 cultured B-cells chr11:64190064..64190065 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_109104,RMVar_hsa_circ_150402 54915 RMVar_ID_54915 Human_SNP_ID_813520759 A-to-I Human chr11 - 6450586 6450586 6450586 CCCATTTTGTGGCTGTGAACAACAAGAATGAAATTGTAGTAACGGACTTCCATAACCATTCAGTG CCCATTTTGTGGCTGTGAACAACAAGAATGAATTTGTAGTAACGGACTTCCATAACCATTCAGTG T A TRIM3 Ensembl:ENSG00000110171 Protein coding CDS GSE100210 HepG2 cell line chr11:6450585..6450586 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,LUSC 7 lung Human_RBP_ID_11668612 Human_Splice_Rec_1204390,Human_Splice_Rec_1204391,Human_Splice_Rec_1204398,Human_Splice_Rec_1204399,Human_Splice_Rec_1204420,Human_Splice_Rec_1204421,Human_Splice_Rec_1204440,Human_Splice_Rec_1204441,Human_Splice_Rec_1204464,Human_Splice_Rec_1204465,Human_Splice_Rec_1204482,Human_Splice_Rec_1204483,Human_Splice_Rec_1204490 RMVar_hsa_circ_11696 54916 RMVar_ID_54916 Human_SNP_ID_813565019 A-to-I Human chr11 - 33157725 33157725 33157725 GAAGTTCAAGTTTGTAGAATAAACCTGATACTATCTTAAATTTATTACTAAAATATATGGATAGT GAAGTTCAAGTTTGTAGAATAAACCTGATACTGTCTTAAATTTATTACTAAAATATATGGATAGT T C CSTF3 Ensembl:ENSG00000176102 Protein coding intron GSE100210 HepG2 cell line chr11:33157724..33157725 29129909 RNA-Seq:(High) rs564998098 Functional Loss SNV ICGC 33..33 33 PBCA 1 - Human_RBP_ID_2266832,Human_RBP_ID_6069271,Human_RBP_ID_9638180,Human_RBP_ID_17795009 RMVar_hsa_circ_99096,RMVar_hsa_circ_148913,RMVar_hsa_circ_148915 54917 RMVar_ID_54917 Human_SNP_ID_813581215 A-to-I Human chr11 + 61852891 61852891 61852891 AAACGTAGTCTCTCGGCCCAGCGTGGTGGCTCACATCTGTAATCCCAGCACTTTGGGAGGCCGAG AAACGTAGTCTCTCGGCCCAGCGTGGTGGCTCGCATCTGTAATCCCAGCACTTTGGGAGGCCGAG A G FADS2 Ensembl:ENSG00000134824 Protein coding intron GSE38233 cultured B-cells chr11:61852890..61852891 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_83513,RMVar_hsa_circ_376556,RMVar_hsa_circ_41699,RMVar_hsa_circ_150092,RMVar_hsa_circ_113767,RMVar_hsa_circ_322001,RMVar_hsa_circ_150098 54918 RMVar_ID_54918 Human_SNP_ID_813607304 A-to-I Human chr11 + 18665022 18665022 18665022 GGAAGGCCCATCGGAGCATGTGGATTTGAGCCACCACATTTTTTAACCCTAGATCTCGAAATGCA GGAAGGCCCATCGGAGCATGTGGATTTGAGCCGCCACATTTTTTAACCCTAGATCTCGAAATGCA A G - - Other Unknown GSE100210 HepG2 cell line chr11:18665021..18665022 29129909 RNA-Seq:(High) rs878858042 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_22790092,Human_RBP_ID_22896087,Human_RBP_ID_26888759 54919 RMVar_ID_54919 Human_SNP_ID_813635084 A-to-I Human chr11 + 108057296 108057296 108057296 GCAGTTCTCCCACCTCGACCTCCCAGAGTGCTAGGATTACAGGCACGAGCCACGGCACTTGGCAG GCAGTTCTCCCACCTCGACCTCCCAGAGTGCTGGGATTACAGGCACGAGCCACGGCACTTGGCAG A G CUL5 Ensembl:ENSG00000166266 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr11:108057295..108057296 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - RMVar_hsa_circ_33769,RMVar_hsa_circ_298184,RMVar_hsa_circ_326927,RMVar_hsa_circ_317351,RMVar_hsa_circ_18486,RMVar_hsa_circ_334417,RMVar_hsa_circ_349084,RMVar_hsa_circ_373159,RMVar_hsa_circ_316121,RMVar_hsa_circ_278592,RMVar_hsa_circ_21799,RMVar_hsa_circ_152823,RMVar_hsa_circ_152825,RMVar_hsa_circ_152826,RMVar_hsa_circ_152827,RMVar_hsa_circ_152824,RMVar_hsa_circ_152830,RMVar_hsa_circ_35432,RMVar_hsa_circ_274033,RMVar_hsa_circ_317849,RMVar_hsa_circ_335485,RMVar_hsa_circ_271262,RMVar_hsa_circ_152832,RMVar_hsa_circ_152833,RMVar_hsa_circ_152831,RMVar_hsa_circ_152828,RMVar_hsa_circ_152829,RMVar_hsa_circ_325339,RMVar_hsa_circ_333692,RMVar_hsa_circ_334745,RMVar_hsa_circ_312086,RMVar_hsa_circ_291185,RMVar_hsa_circ_309912,RMVar_hsa_circ_93465,RMVar_hsa_circ_33750,RMVar_hsa_circ_152836,RMVar_hsa_circ_152838,RMVar_hsa_circ_152840,RMVar_hsa_circ_44439,RMVar_hsa_circ_152841,RMVar_hsa_circ_152839,RMVar_hsa_circ_152837,RMVar_hsa_circ_36598,RMVar_hsa_circ_40990,RMVar_hsa_circ_60796 54920 RMVar_ID_54920 Human_SNP_ID_813673573 A-to-I Human chr11 + 67146648 67146648 67146648 CTCCTGCCTCAGCCCCACAAGTACCAGGGACTACAGGTGCTTACCACTACACCTGGCTAATTTTT CTCCTGCCTCAGCCCCACAAGTACCAGGGACTGCAGGTGCTTACCACTACACCTGGCTAATTTTT A G KDM2A Ensembl:ENSG00000173120 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr11:67146647..67146648 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast HER-positive_carcinoma 4 breast RMVar_hsa_circ_4595,RMVar_hsa_circ_72699,RMVar_hsa_circ_151014,RMVar_hsa_circ_357875,RMVar_hsa_circ_330836,RMVar_hsa_circ_41037,RMVar_hsa_circ_53993,RMVar_hsa_circ_23665 54921 RMVar_ID_54921 Human_SNP_ID_813763343 A-to-I Human chr11 + 112230638 112230638 112230638 CACCTTTGTTTATTCTTTAGATTGACCCTGCTACGGGAATGGTTATGAATCTGGCTGATCTCAAA CACCTTTGTTTATTCTTTAGATTGACCCTGCTGCGGGAATGGTTATGAATCTGGCTGATCTCAAA A G PTS Ensembl:ENSG00000150787 Protein coding 3'UTR GSE100210 HepG2 cell line chr11:112230637..112230638 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver hepatocellular_carcinoma 4 liver Human_RBP_ID_389007,Human_RBP_ID_866172,Human_RBP_ID_4187804,Human_RBP_ID_5344433,Human_RBP_ID_9344143,Human_RBP_ID_22538357,Human_RBP_ID_22643837,Human_RBP_ID_23486448,Human_RBP_ID_24912777 Human_Splice_Rec_1298108,Human_Splice_Rec_1298109,Human_Splice_Rec_1298118,Human_Splice_Rec_1298119,Human_Splice_Rec_1298132,Human_Splice_Rec_1298133,Human_Splice_Rec_1298148,Human_Splice_Rec_1298149,Human_Splice_Rec_1298154,Human_Splice_Rec_1298155,Human_Splice_Rec_1298157,Human_Splice_Rec_1298161 RMVar_hsa_circ_57989,RMVar_hsa_circ_352942 54922 RMVar_ID_54922 Human_SNP_ID_813781835 A-to-I Human chr11 - 85998883 85998883 85998883 GTGGTGGCGTGTGCCTGTTGTCCCAGCTACTCAGGAGGTTGAGGCAGGAGGAAGGCCTGAGCCCA GTGGTGGCGTGTGCCTGTTGTCCCAGCTACTCGGGAGGTTGAGGCAGGAGGAAGGCCTGAGCCCA T C PICALM Ensembl:ENSG00000073921 Protein coding intron GSE100210 HepG2 cell line chr11:85998882..85998883 29129909 RNA-Seq:(High) rs540506285 Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_152257,RMVar_hsa_circ_368290,RMVar_hsa_circ_373209,RMVar_hsa_circ_295279,RMVar_hsa_circ_286180,RMVar_hsa_circ_272337,RMVar_hsa_circ_272743,RMVar_hsa_circ_119740,RMVar_hsa_circ_15803,RMVar_hsa_circ_7852,RMVar_hsa_circ_152240,RMVar_hsa_circ_152241,RMVar_hsa_circ_108911,RMVar_hsa_circ_152238,RMVar_hsa_circ_152239,RMVar_hsa_circ_152237,RMVar_hsa_circ_92742,RMVar_hsa_circ_57042,RMVar_hsa_circ_152251,RMVar_hsa_circ_152252,RMVar_hsa_circ_342236,RMVar_hsa_circ_357005,RMVar_hsa_circ_346191,RMVar_hsa_circ_332531,RMVar_hsa_circ_322833,RMVar_hsa_circ_284486,RMVar_hsa_circ_280441,RMVar_hsa_circ_52067,RMVar_hsa_circ_152259,RMVar_hsa_circ_152260,RMVar_hsa_circ_152258,RMVar_hsa_circ_32368,RMVar_hsa_circ_152269,RMVar_hsa_circ_7129,RMVar_hsa_circ_299460,RMVar_hsa_circ_114749,RMVar_hsa_circ_83938,RMVar_hsa_circ_152270,RMVar_hsa_circ_51418,RMVar_hsa_circ_100199,RMVar_hsa_circ_152268,RMVar_hsa_circ_152280,RMVar_hsa_circ_320251,RMVar_hsa_circ_152278,RMVar_hsa_circ_368945,RMVar_hsa_circ_370213,RMVar_hsa_circ_357923,RMVar_hsa_circ_274205,RMVar_hsa_circ_91665,RMVar_hsa_circ_65207,RMVar_hsa_circ_298472,RMVar_hsa_circ_303125,RMVar_hsa_circ_152279,RMVar_hsa_circ_303012,RMVar_hsa_circ_294372,RMVar_hsa_circ_64875,RMVar_hsa_circ_152284,RMVar_hsa_circ_152288,RMVar_hsa_circ_279395,RMVar_hsa_circ_152281,RMVar_hsa_circ_152282,RMVar_hsa_circ_281534,RMVar_hsa_circ_310150,RMVar_hsa_circ_329871,RMVar_hsa_circ_297237,RMVar_hsa_circ_279738,RMVar_hsa_circ_271167,RMVar_hsa_circ_275317,RMVar_hsa_circ_55198,RMVar_hsa_circ_152286,RMVar_hsa_circ_152287,RMVar_hsa_circ_152285,RMVar_hsa_circ_152283 54923 RMVar_ID_54923 Human_SNP_ID_813852269 A-to-I Human chr11 + 67228856 67228856 67228856 ACTCCTGGGCTCAAGCAATCCCCCTCCTGAGTAACTAGGATTACAAGCACACACCACTATGCCCA ACTCCTGGGCTCAAGCAATCCCCCTCCTGAGTTACTAGGATTACAAGCACACACCACTATGCCCA A T KDM2A Ensembl:ENSG00000173120 Protein coding intron GSE38233 cultured B-cells chr11:67228856..67228857 24183664 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 3 prostate RMVar_hsa_circ_72699,RMVar_hsa_circ_354083,RMVar_hsa_circ_284707,RMVar_hsa_circ_265098,RMVar_hsa_circ_49948,RMVar_hsa_circ_115497,RMVar_hsa_circ_151030,RMVar_hsa_circ_296943,RMVar_hsa_circ_364268,RMVar_hsa_circ_151021,RMVar_hsa_circ_91208,RMVar_hsa_circ_367294,RMVar_hsa_circ_151031,RMVar_hsa_circ_295185,RMVar_hsa_circ_151034 54924 RMVar_ID_54924 Human_SNP_ID_813882100 A-to-I Human chr11 - 103050785 103050785 103050785 CTTGAGAGCAGGGACTGTGTGTTTTTGCTTTTATTTCACCAGTACTCAGAACTATCCACAGTATA CTTGAGAGCAGGGACTGTGTGTTTTTGCTTTTGTTTCACCAGTACTCAGAACTATCCACAGTATA T C DCUN1D5,AP001486.2 Ensembl:ENSG00000137692,Ensembl:ENSG00000260966 Protein coding,lincRNA 3'UTR,exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr11:103050785..103050786 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_RBP_ID_2247109,Human_RBP_ID_6037113,Human_RBP_ID_11505127 54925 RMVar_ID_54925 Human_SNP_ID_813926305 A-to-I Human chr11 - 123018184 123018184 123018184 TCAGGCCCATCTTCTACTCCTTGGCTAACTTTAGCAACTTTAGTTTTCTCCTCTACAAACTCATG TCAGGCCCATCTTCTACTCCTTGGCTAACTTTGGCAACTTTAGTTTTCTCCTCTACAAACTCATG T C - - Other Unknown GSE100210 HepG2 cell line chr11:123018183..123018184 29129909 RNA-Seq:(High) rs879082202 Functional Loss SNV TCGA,ICGC 33..33 33 LAML,LUSC 3 - 54926 RMVar_ID_54926 Human_SNP_ID_813930334 A-to-I Human chr11 + 63822153 63822147 63822154 TTGCCTGAGGCTAGGTGTTCGAGACCAACCTGAGCAACATAAGGAGACTCCATCTCTAGAAAAAT TTGCCTGAGGCTAGGTGTTCGAGACCA_______CAACATAAGGAGACTCCATCTCTAGAAAAAT AACCTGAG A SPINDOC Ensembl:ENSG00000168005 Protein coding intron GSE100210 HepG2 cell line chr11:63822152..63822153 29129909 RNA-Seq:(High) - Functional Loss DEL ICGC 28..34 33 RECA 1 - Human_RBP_ID_6083754 RMVar_hsa_circ_78377,RMVar_hsa_circ_150371,RMVar_hsa_circ_97315,RMVar_hsa_circ_150372,RMVar_hsa_circ_150378,RMVar_hsa_circ_101809 54927 RMVar_ID_54927 Human_SNP_ID_877103582 A-to-I Human chr9 - 128112080 128112080 128112080 GCACGTGCCACCACACCCAGTTAATTTTTTGTATTTTTAGTAGAGATGGGGTTTCACCGGGTTAG GCACGTGCCACCACACCCAGTTAATTTTTTGTGTTTTTAGTAGAGATGGGGTTTCACCGGGTTAG T C SLC25A25-AS1 Ensembl:ENSG00000234771 lincRNA exon GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells chr9:128112079..128112080 23474544,24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - RMVar_hsa_circ_107826,RMVar_hsa_circ_259837 54928 RMVar_ID_54928 Human_SNP_ID_877106292 A-to-I Human chr9 + 122428346 122428346 122428346 CTGCTCGCTGCAGCCTCTGTCTCCCGGGTTCGAGTGATTCTCCTGCCTCAGCCTCGCGAGTAGTT CTGCTCGCTGCAGCCTCTGTCTCCCGGGTTCGTGTGATTCTCCTGCCTCAGCCTCGCGAGTAGTT A T AL359636.2 Ensembl:ENSG00000234156 lincRNA intron GSE100210 HepG2 cell line chr9:122428345..122428346 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - 54929 RMVar_ID_54929 Human_SNP_ID_877160861 A-to-I Human chr9 + 128331674 128331674 128331674 TCAAGCATCCTCCTGTCCCAAGCCTCCTGAGTAGCTGGGACTATAGGCACACACCACCACACCTG TCAAGCATCCTCCTGTCCCAAGCCTCCTGAGTGGCTGGGACTATAGGCACACACCACCACACCTG A G COQ4 Ensembl:ENSG00000167113 Protein coding intron GSE100210;GSE126723:GSM3611827,GSM3611828,GSM3611829 HepG2 cell line;Bronchiolar epithelium,BEP2D cell line chr9:128331673..128331674 29129909,31158229 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 RECA 1 - RMVar_hsa_circ_96189,RMVar_hsa_circ_124412,RMVar_hsa_circ_259901,RMVar_hsa_circ_259902,RMVar_hsa_circ_81783,RMVar_hsa_circ_259905,RMVar_hsa_circ_259909,RMVar_hsa_circ_107447 54930 RMVar_ID_54930 Human_SNP_ID_877176219 A-to-I Human chr9 - 128112809 128112809 128112809 AAATTCAGGTATGGCCGGGCACGGTGGCTCACACCTGTAATCCCAGCACTTTGGGAGGCCAAGGT AAATTCAGGTATGGCCGGGCACGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGT T C SLC25A25-AS1 Ensembl:ENSG00000234771 lincRNA intron GSE100210 HepG2 cell line chr9:128112808..128112809 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 STAD 1 - RMVar_hsa_circ_107826,RMVar_hsa_circ_259837 54931 RMVar_ID_54931 Human_SNP_ID_877230874 A-to-I Human chr9 - 68235001 68235001 68235001 TGTCCTCCTGAGGGGATGAACACTGTGTGTTCACCTGGCAGAAGGAGACAGAAATAAGCTTTCAC TGTCCTCCTGAGGGGATGAACACTGTGTGTTCGCCTGGCAGAAGGAGACAGAAATAAGCTTTCAC T C - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr9:68235000..68235001 30559470 RNA-Seq:(High) rs797035381 Functional Loss SNV ICGC 33..33 33 LUSC 1 - 54932 RMVar_ID_54932 Human_SNP_ID_877249978 A-to-I Human chr9 - 5625450 5625450 5625450 CCAGCACTTTCGGAGGCAGAGGTGGGCGGATCACTTGAGCCCGGGAGTTTGAGACCAGCCTGGGC CCAGCACTTTCGGAGGCAGAGGTGGGCGGATCGCTTGAGCCCGGGAGTTTGAGACCAGCCTGGGC T C AL162253.2 Ensembl:ENSG00000286162 lincRNA intron GSE100210 HepG2 cell line chr9:5625449..5625450 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 54933 RMVar_ID_54933 Human_SNP_ID_877253680 A-to-I Human chr9 - 129913236 129913236 129913236 GTCCAGTGTGGTAGCCACTACCATATGTAGCTATTGAGTTTTTTGTTTTTGTTTTTGTTTTGAGA GTCCAGTGTGGTAGCCACTACCATATGTAGCTGTTGAGTTTTTTGTTTTTGTTTTTGTTTTGAGA T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells chr9:129913235..129913236 24183664 RNA-Seq:(High) rs7029572 Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 4 liver GWAS_ID_5925,GWAS_ID_5926,GWAS_ID_5927,GWAS_ID_5928,GWAS_ID_5929,GWAS_ID_5930,GWAS_ID_5931,GWAS_ID_5932,GWAS_ID_5933,GWAS_ID_5934,GWAS_ID_5935,GWAS_ID_5936,GWAS_ID_5937,GWAS_ID_5938,GWAS_ID_5939,GWAS_ID_5940,GWAS_ID_5941,GWAS_ID_5942,GWAS_ID_5943,GWAS_ID_5944,GWAS_ID_5945,GWAS_ID_5946,GWAS_ID_5947,GWAS_ID_5948,GWAS_ID_5949,GWAS_ID_5950,GWAS_ID_5951,GWAS_ID_5952,GWAS_ID_5953,GWAS_ID_5954,GWAS_ID_5955,GWAS_ID_5956,GWAS_ID_5957,GWAS_ID_5958,GWAS_ID_5959,GWAS_ID_5960,GWAS_ID_5961,GWAS_ID_5962,GWAS_ID_5963,GWAS_ID_5964,GWAS_ID_5965,GWAS_ID_5966,GWAS_ID_5967,GWAS_ID_5968,GWAS_ID_5969,GWAS_ID_5970,GWAS_ID_5971,GWAS_ID_5972,GWAS_ID_5973,GWAS_ID_5974,GWAS_ID_5975,GWAS_ID_5976,GWAS_ID_5977,GWAS_ID_5978,GWAS_ID_5979,GWAS_ID_5980,GWAS_ID_5981,GWAS_ID_5982,GWAS_ID_5983,GWAS_ID_5984,GWAS_ID_5985,GWAS_ID_5986,GWAS_ID_5987,GWAS_ID_5988,GWAS_ID_5989,GWAS_ID_5990,GWAS_ID_5991,GWAS_ID_5992,GWAS_ID_5993,GWAS_ID_5994,GWAS_ID_5995,GWAS_ID_5996,GWAS_ID_5997,GWAS_ID_5998,GWAS_ID_5999,GWAS_ID_6000,GWAS_ID_6001,GWAS_ID_6002,GWAS_ID_6003,GWAS_ID_6004 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_260279,RMVar_hsa_circ_260280,RMVar_hsa_circ_260278 54934 RMVar_ID_54934 Human_SNP_ID_877432719 A-to-I Human chr9 - 154795 154795 154795 GTTTCTTAACATTTCTCTGTTTGCTATTTTAGACAAGTTGCTTTGGCAGATGCCATTCTCATTAA GTTTCTTAACATTTCTCTGTTTGCTATTTTAGGCAAGTTGCTTTGGCAGATGCCATTCTCATTAA T C CBWD1 Ensembl:ENSG00000172785 Protein coding CDS GSE105773 Glioblastoma cells,U87MG chr9:154794..154795 29724793 RNA-Seq:(High) rs2785333 Functional Loss SNV ICGC,COSMIC 33..33 33 COCA,skin basal_cell_carcinoma,liver neoplasm,liver hepatocellular_carcinoma 40 liver,skin Human_Splice_Rec_1025894,Human_Splice_Rec_1025895,Human_Splice_Rec_1025922,Human_Splice_Rec_1025923,Human_Splice_Rec_1025948,Human_Splice_Rec_1025949,Human_Splice_Rec_1025978,Human_Splice_Rec_1025979,Human_Splice_Rec_1026102,Human_Splice_Rec_1026103,Human_Splice_Rec_1026124,Human_Splice_Rec_1026125,Human_Splice_Rec_1026154,Human_Splice_Rec_1026155,Human_Splice_Rec_1026194,Human_Splice_Rec_1026195,Human_Splice_Rec_1026220,Human_Splice_Rec_1026221,Human_Splice_Rec_1026238,Human_Splice_Rec_1026239,Human_Splice_Rec_1026250,Human_Splice_Rec_1026251,Human_Splice_Rec_1026278,Human_Splice_Rec_1026279,Human_Splice_Rec_1026284,Human_Splice_Rec_1026285,Human_Splice_Rec_1026296,Human_Splice_Rec_1026297,Human_Splice_Rec_1026312,Human_Splice_Rec_1026322 RMVar_hsa_circ_64156,RMVar_hsa_circ_36154,RMVar_hsa_circ_371776,RMVar_hsa_circ_255219,RMVar_hsa_circ_2994,RMVar_hsa_circ_311748,RMVar_hsa_circ_357198,RMVar_hsa_circ_65925,RMVar_hsa_circ_25594,RMVar_hsa_circ_69511,RMVar_hsa_circ_320223,RMVar_hsa_circ_73448 54935 RMVar_ID_54935 Human_SNP_ID_877457267 A-to-I Human chr9 - 83677787 83677787 83677787 CTGCCAGCACTGTGGGTGGCACTACTGGTAGTACTGCCAGTGGCACTTCTGGGCAGAGTACTACT CTGCCAGCACTGTGGGTGGCACTACTGGTAGTGCTGCCAGTGGCACTTCTGGGCAGAGTACTACT T C UBQLN1 Ensembl:ENSG00000135018 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector chr9:83677786..83677787 29967493 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PAAD,pancreas ductal_carcinoma 3 pancreas Human_RBP_ID_1706466,Human_RBP_ID_7940545,Human_RBP_ID_9314844,Human_RBP_ID_16718539,Human_RBP_ID_17322913,Human_RBP_ID_17437085,Human_RBP_ID_26833279 Human_Splice_Rec_1056461,Human_Splice_Rec_1056479,Human_Splice_Rec_1056497 RMVar_hsa_circ_257412,RMVar_hsa_circ_64274,RMVar_hsa_circ_257402,RMVar_hsa_circ_257398,RMVar_hsa_circ_106466,RMVar_hsa_circ_82923,RMVar_hsa_circ_84247,RMVar_hsa_circ_78767,RMVar_hsa_circ_257400,RMVar_hsa_circ_257401,RMVar_hsa_circ_257399,RMVar_hsa_circ_335685,RMVar_hsa_circ_278466,RMVar_hsa_circ_14758,RMVar_hsa_circ_257410,RMVar_hsa_circ_257408,RMVar_hsa_circ_281760,RMVar_hsa_circ_275132,RMVar_hsa_circ_99008,RMVar_hsa_circ_257409,RMVar_hsa_circ_62064,RMVar_hsa_circ_285962,RMVar_hsa_circ_374410,RMVar_hsa_circ_257411,RMVar_hsa_circ_373398,RMVar_hsa_circ_257414,RMVar_hsa_circ_257413,RMVar_hsa_circ_257416,RMVar_hsa_circ_257420,RMVar_hsa_circ_280455,RMVar_hsa_circ_285639,RMVar_hsa_circ_292901,RMVar_hsa_circ_282426,RMVar_hsa_circ_276748,RMVar_hsa_circ_257418,RMVar_hsa_circ_257419,RMVar_hsa_circ_257417 54936 RMVar_ID_54936 Human_SNP_ID_877489315 A-to-I Human chr9 - 4739845 4739828 4739845 AGTCTTGCTCTGTCTGCCTCCTGGGTTCAAGCAATTCTCCTGTCTCAGCCTCCCTAGTAGCTGGG AGTCTTGCTCTGTCTGCCTCCTGGGTTCAAGC_________________CTCCCTAGTAGCTGGG GGCTGAGACAGGAGAATT G AK3 Ensembl:ENSG00000147853 Protein coding intron GSE38233 cultured B-cells chr9:4739844..4739845 24183664 RNA-Seq:(High) - Functional Loss DEL ICGC 33..49 33 BRCA 1 - Human_RBP_ID_16683637 RMVar_hsa_circ_103274,RMVar_hsa_circ_255436 54937 RMVar_ID_54937 Human_SNP_ID_877489315 A-to-I Human chr9 - 4739844 4739828 4739845 GTCTTGCTCTGTCTGCCTCCTGGGTTCAAGCAATTCTCCTGTCTCAGCCTCCCTAGTAGCTGGGA GTCTTGCTCTGTCTGCCTCCTGGGTTCAAGC_________________CTCCCTAGTAGCTGGGA GGCTGAGACAGGAGAATT G AK3 Ensembl:ENSG00000147853 Protein coding intron GSE38233 cultured B-cells chr9:4739843..4739844 24183664 RNA-Seq:(High) - Functional Loss DEL ICGC 32..48 33 BRCA 1 - Human_RBP_ID_16683637 RMVar_hsa_circ_103274,RMVar_hsa_circ_255436 54938 RMVar_ID_54938 Human_SNP_ID_877503661 A-to-I Human chr9 + 130704287 130704287 130704287 CACGGTGGCTCACGCCTATAATCCCAGCACTTAGGGAGGCCAAGGCGGGCAGATCACCTGAGGTC CACGGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGCCAAGGCGGGCAGATCACCTGAGGTC A T EXOSC2 Ensembl:ENSG00000130713 Protein coding 3'UTR GSE38233;GSE99789;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BEP2D cell line chr9:130704286..130704287 24183664,29796672,31158229 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PRAD 1 - Human_RBP_ID_23090475 Human_miRNA_ID_2217753,Human_miRNA_ID_2315728,Human_miRNA_ID_2318884,Human_miRNA_ID_2322045,Human_miRNA_ID_2325211,Human_miRNA_ID_2328330,Human_miRNA_ID_2519588,Human_miRNA_ID_2522753,Human_miRNA_ID_2821947,Human_miRNA_ID_2828077,Human_miRNA_ID_2831233,Human_miRNA_ID_2835353,Human_miRNA_ID_2840709 RMVar_hsa_circ_91666,RMVar_hsa_circ_260347,RMVar_hsa_circ_123461,RMVar_hsa_circ_260350 54939 RMVar_ID_54939 Human_SNP_ID_877558602 A-to-I Human chr9 + 133052089 133052089 133052089 CAGCTGTTTGACATCCGTCCCATCTGGTCCCGAAATGCTGTCAAGGCCAACATCAGCGTCCACCC CAGCTGTTTGACATCCGTCCCATCTGGTCCCGGAATGCTGTCAAGGCCAACATCAGCGTCCACCC A G GTF3C5 Ensembl:ENSG00000148308 Protein coding CDS GSE100210 HepG2 cell line chr9:133052088..133052089 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA,ICGC,COSMIC 33..33 33 COAD,caecum adenocarcinoma,large_intestine adenocarcinoma 6 caecum,large intestine Human_RBP_ID_714140,Human_RBP_ID_8699138,Human_RBP_ID_19024526,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 54940 RMVar_ID_54940 Human_SNP_ID_877576499 A-to-I Human chr9 + 129125893 129125893 129125893 GCTTTTGGCTGGGCGCGGTGGCTCATGACTGTAATCCTAGCACCTTGGGAGGCCAAGGCGGGTGA GCTTTTGGCTGGGCGCGGTGGCTCATGACTGTTATCCTAGCACCTTGGGAGGCCAAGGCGGGTGA A T PTPA Ensembl:ENSG00000119383 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr9:129125892..129125893;chr9:129125893..129125894 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_93454,RMVar_hsa_circ_98099,RMVar_hsa_circ_260227,RMVar_hsa_circ_260229,RMVar_hsa_circ_260228,RMVar_hsa_circ_44760,RMVar_hsa_circ_115240,RMVar_hsa_circ_33272,RMVar_hsa_circ_347910,RMVar_hsa_circ_27350 54941 RMVar_ID_54941 Human_SNP_ID_877643597 A-to-I Human chr9 + 100129387 100129387 100129387 GGGCATGGTCGTGAGCACGTGTACTCCCAGCTACTTGGGAGGCTGAGGTGGAAGGGTCGCTTGAG GGGCATGGTCGTGAGCACGTGTACTCCCAGCTGCTTGGGAGGCTGAGGTGGAAGGGTCGCTTGAG A G INVS Ensembl:ENSG00000119509 Protein coding intron GSE100210 HepG2 cell line chr9:100129386..100129387 29129909 RNA-Seq:(High) - 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_322086,RMVar_hsa_circ_258261 54942 RMVar_ID_54942 Human_SNP_ID_877655909 A-to-I Human chr9 + 128326953 128326953 128326953 GTACTTTTAGTAGAGAGGGGTTTTACCATATTAACCAGGCTGGTCTTGAACTCCTGACCTCAAGT GTACTTTTAGTAGAGAGGGGTTTTACCATATTGACCAGGCTGGTCTTGAACTCCTGACCTCAAGT A G COQ4 Ensembl:ENSG00000167113 Protein coding intron GSE38233;GSE99789 cultured B-cells;esophageal squamous carcinoma cells,EC109 chr9:128326952..128326953 24183664,29796672 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 LICA,liver neoplasm 2 liver RMVar_hsa_circ_96189,RMVar_hsa_circ_124412,RMVar_hsa_circ_259901,RMVar_hsa_circ_259902,RMVar_hsa_circ_81783,RMVar_hsa_circ_259905,RMVar_hsa_circ_259909,RMVar_hsa_circ_107447 54943 RMVar_ID_54943 Human_SNP_ID_877699469 A-to-I Human chr9 + 97602542 97602542 97602542 GCTCTGGGCTCACAGGCTGTCGCACATGCTGCAAGAGTTCCCTAGGTATGCGTGGCCGTCGGGCT GCTCTGGGCTCACAGGCTGTCGCACATGCTGCGAGAGTTCCCTAGGTATGCGTGGCCGTCGGGCT A G - - Other Unknown GSE100210 HepG2 cell line chr9:97602541..97602542 29129909 RNA-Seq:(High) rs749218582 Functional Loss SNV COSMIC 33..33 33 pharynx nasopharyngeal_carcinoma 1 head and neck 54944 RMVar_ID_54944 Human_SNP_ID_877734300 A-to-I Human chr9 + 92595451 92595451 92595451 TTTGTGGAGATGGGGATCTTACCTTGTTGCCCAAGCTGGTCCTGAACTCCTGACCTCAAGCAATC TTTGTGGAGATGGGGATCTTACCTTGTTGCCCGAGCTGGTCCTGAACTCCTGACCTCAAGCAATC A G CENPP Ensembl:ENSG00000188312 Protein coding intron GSE100210 HepG2 cell line chr9:92595451..92595452 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 2 ovary Human_RBP_ID_16738972 54945 RMVar_ID_54945 Human_SNP_ID_877787887 A-to-I Human chr9 - 61857069 61857069 61857069 GACCTGGTAGCCCTGACGCAACTTCGGCTGGCACAAACCCACAGAGAGTGGGAAAGAAACACACA GACCTGGTAGCCCTGACGCAACTTCGGCTGGCTCAAACCCACAGAGAGTGGGAAAGAAACACACA T A - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr9:61857068..61857069 30559470 RNA-Seq:(High) rs1218754531 Functional Loss SNV ICGC 33..33 33 LUSC 3 - 54946 RMVar_ID_54946 Human_SNP_ID_877849169 A-to-I Human chr9 - 112271536 112271536 112271536 GTGTGATTTTAGTAGAGAAGGGGTTACACCACATTGGCTAGGCTGGTCTCAAACTCCTAACCTCA GTGTGATTTTAGTAGAGAAGGGGTTACACCACGTTGGCTAGGCTGGTCTCAAACTCCTAACCTCA T C PTBP3 Ensembl:ENSG00000119314 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr9:112271535..112271536 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LUSC 1 - RMVar_hsa_circ_258807,RMVar_hsa_circ_335599,RMVar_hsa_circ_301605,RMVar_hsa_circ_258796,RMVar_hsa_circ_337391,RMVar_hsa_circ_31594,RMVar_hsa_circ_258797,RMVar_hsa_circ_106257,RMVar_hsa_circ_258803,RMVar_hsa_circ_69431,RMVar_hsa_circ_346336,RMVar_hsa_circ_368049,RMVar_hsa_circ_258806,RMVar_hsa_circ_285015,RMVar_hsa_circ_328218,RMVar_hsa_circ_270519,RMVar_hsa_circ_258808,RMVar_hsa_circ_258822,RMVar_hsa_circ_258818,RMVar_hsa_circ_258812,RMVar_hsa_circ_258814,RMVar_hsa_circ_303727,RMVar_hsa_circ_326181,RMVar_hsa_circ_284809,RMVar_hsa_circ_258813,RMVar_hsa_circ_273536,RMVar_hsa_circ_323463,RMVar_hsa_circ_258820,RMVar_hsa_circ_271013,RMVar_hsa_circ_258819,RMVar_hsa_circ_272097,RMVar_hsa_circ_377625,RMVar_hsa_circ_258824,RMVar_hsa_circ_270096,RMVar_hsa_circ_258823 54947 RMVar_ID_54947 Human_SNP_ID_877849216 A-to-I Human chr9 - 33120025 33120025 33120025 CACTTGCCACCATGCGCAGCTAATTTTTGTATATTTTGTAGAGATGGGGTTTTGCTGTATTGCCC CACTTGCCACCATGCGCAGCTAATTTTTGTATGTTTTGTAGAGATGGGGTTTTGCTGTATTGCCC T C B4GALT1 Ensembl:ENSG00000086062 Protein coding intron GSE47997 K562 cells&HepG2 cells chr9:33120024..33120025 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - RMVar_hsa_circ_113644,RMVar_hsa_circ_97414,RMVar_hsa_circ_91506,RMVar_hsa_circ_256330,RMVar_hsa_circ_256331,RMVar_hsa_circ_256332,RMVar_hsa_circ_256333,RMVar_hsa_circ_319028 54948 RMVar_ID_54948 Human_SNP_ID_877866676 A-to-I Human chr9 - 127523729 127523729 127523729 CTACTACTTCTGCATGATGACAGAAGCCGAGCAGGACAAGTGGCAGGCTGTGCTGCAGGACTGCA CTACTACTTCTGCATGATGACAGAAGCCGAGCTGGACAAGTGGCAGGCTGTGCTGCAGGACTGCA T A NIBAN2 Ensembl:ENSG00000136830 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector chr9:127523728..127523729 29967493 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 2 liver Human_RBP_ID_22467075,Human_RBP_ID_26833555 Human_Splice_Rec_1082273,Human_Splice_Rec_1082303 Human_miRNA_ID_2254775 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 54949 RMVar_ID_54949 Human_SNP_ID_877954934 A-to-I Human chr9 + 98013897 98013897 98013897 AAAAAGTTAGCTGCACATGGTGGTGCACACCTATAGTCCCAGCTACTTGGGAAGCTGAGGTGGGA AAAAAGTTAGCTGCACATGGTGGTGCACACCTCTAGTCCCAGCTACTTGGGAAGCTGAGGTGGGA A C ANP32B Ensembl:ENSG00000136938 Protein coding intron GSE47997;GSE38233 K562 cells&HepG2 cells;cultured B-cells chr9:98013896..98013897 23474544,24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 54950 RMVar_ID_54950 Human_SNP_ID_877996083 A-to-I Human chr9 - 33466216 33466216 33466216 GACCTCTGACTCTTCTTCCTCAGTGGTTTGTCACCTGGAGGGCAGTGGCCAGTGGCCACAGGACG GACCTCTGACTCTTCTTCCTCAGTGGTTTGTCGCCTGGAGGGCAGTGGCCAGTGGCCACAGGACG T C NOL6 Ensembl:ENSG00000165271 Protein coding CDS GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr9:33466216..33466217 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 ESCA,endometrium endometrioid_carcinoma 2 uterus Human_RBP_ID_962006,Human_RBP_ID_3975345,Human_RBP_ID_5535327,Human_RBP_ID_8929945,Human_RBP_ID_9315461,Human_RBP_ID_18173143,Human_RBP_ID_19023750 Human_Splice_Rec_1038526,Human_Splice_Rec_1038616 RMVar_hsa_circ_104163,RMVar_hsa_circ_256375,RMVar_hsa_circ_98355,RMVar_hsa_circ_256377,RMVar_hsa_circ_107840,RMVar_hsa_circ_256378,RMVar_hsa_circ_25104,RMVar_hsa_circ_125214,RMVar_hsa_circ_256381 54951 RMVar_ID_54951 Human_SNP_ID_877997879 A-to-I Human chr9 - 123869942 123869942 123869942 CACTCTTACATAACAGTTTCAATGGCGTGATCATGGTTCACTGCAGCTTTGACCTTCCAGACTTA CACTCTTACATAACAGTTTCAATGGCGTGATCGTGGTTCACTGCAGCTTTGACCTTCCAGACTTA T C DENND1A Ensembl:ENSG00000119522 Protein coding intron GSE100210 HepG2 cell line chr9:123869941..123869942 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 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,RMVar_hsa_circ_259434 54952 RMVar_ID_54952 Human_SNP_ID_878009078 A-to-I Human chr9 + 130700100 130700100 130700100 CAGACTGGAGTGCAGTGGCGCGATCTCGGCTCACTGCAACGTCCGCCTCTTGGATTCAAGCAATT CAGACTGGAGTGCAGTGGCGCGATCTCGGCTCGCTGCAACGTCCGCCTCTTGGATTCAAGCAATT A G EXOSC2 Ensembl:ENSG00000130713 Protein coding intron GSE38233;GSE100210;GSE99789;GSE126723:GSM3611833,GSM3611834,GSM3611835 cultured B-cells;HepG2 cell line;esophageal squamous carcinoma cells,EC109;Bronchiolar epithelium,BERP35T4 cell line chr9:130700099..130700100 24183664,29129909,29796672,31158229 RNA-Seq:(High) rs900740109 Functional Loss SNV ICGC 33..33 33 PBCA 1 - RMVar_hsa_circ_27697,RMVar_hsa_circ_118964,RMVar_hsa_circ_260348,RMVar_hsa_circ_91666,RMVar_hsa_circ_260347,RMVar_hsa_circ_123461,RMVar_hsa_circ_260350 54953 RMVar_ID_54953 Human_SNP_ID_878025777 A-to-I Human chr9 + 128632018 128632018 128632018 CTATTCCTATTCTAGAATGTTCTTGTTTTACGAGGTCTCAGGCCAGGCCTGGAGCAGGAACCAGA CTATTCCTATTCTAGAATGTTCTTGTTTTACGTGGTCTCAGGCCAGGCCTGGAGCAGGAACCAGA A T SPTAN1 Ensembl:ENSG00000197694 Protein coding intron GSE38233 cultured B-cells chr9:128632017..128632018 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 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_90080,RMVar_hsa_circ_260041,RMVar_hsa_circ_79030,RMVar_hsa_circ_260042,RMVar_hsa_circ_111172,RMVar_hsa_circ_260044,RMVar_hsa_circ_260045 54954 RMVar_ID_54954 Human_SNP_ID_878072190 A-to-I Human chr9 + 129004044 129004044 129004044 TCACGCCTGTAATCCCAGCACTTTGGGAATTCAAGGCGGGAGGATCATGAGGTCAGGAGCTCGAG TCACGCCTGTAATCCCAGCACTTTGGGAATTCGAGGCGGGAGGATCATGAGGTCAGGAGCTCGAG A G NUP188 Ensembl:ENSG00000095319 Protein coding intron GSE100210 HepG2 cell line chr9:129004043..129004044 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 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_109440,RMVar_hsa_circ_260158,RMVar_hsa_circ_98205,RMVar_hsa_circ_119813,RMVar_hsa_circ_260171,RMVar_hsa_circ_260172,RMVar_hsa_circ_98396,RMVar_hsa_circ_260192,RMVar_hsa_circ_93220,RMVar_hsa_circ_260194 54955 RMVar_ID_54955 Human_SNP_ID_878156919 A-to-I Human chr9 - 77874795 77874783 77874795 CCAACATGGCGAAACCTCTACTAAAAATTCAAAAAATTAGTCAAGCATGGTGGCACACACCTGTA CCAACATGGCGAAACCTCTACTAAAAATTCAA____________GCATGGTGGCACACACCTGTA CTTGACTAATTTT C GNAQ Ensembl:ENSG00000156052 Protein coding intron GSE47997 K562 cells&HepG2 cells chr9:77874794..77874795 23474544 RNA-Seq:(High) - Functional Loss DEL ICGC 33..44 33 PAAD 1 - RMVar_hsa_circ_51040,RMVar_hsa_circ_330530,RMVar_hsa_circ_271109,RMVar_hsa_circ_257280 54956 RMVar_ID_54956 Human_SNP_ID_878168560 A-to-I Human chr9 - 129980113 129980113 129980113 TCAGGTGATCTGTCTGCCACGGCCTCCAAAGTACTGGGATTACAGGCGTGAGCCACTGTGCCCGG TCAGGTGATCTGTCTGCCACGGCCTCCAAAGTGCTGGGATTACAGGCGTGAGCCACTGTGCCCGG T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells chr9:129980112..129980113 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_69780,RMVar_hsa_circ_359498,RMVar_hsa_circ_55216,RMVar_hsa_circ_30836,RMVar_hsa_circ_260288,RMVar_hsa_circ_260287,RMVar_hsa_circ_288850,RMVar_hsa_circ_299047,RMVar_hsa_circ_260289 54957 RMVar_ID_54957 Human_SNP_ID_878204123 A-to-I Human chr9 - 109160960 109160960 109160960 ATGGTGAAACCTGTCTCTACAAAAATACAAAAATTAGCCGGGCATGATGGCGGGTGCCTGTAATC ATGGTGAAACCTGTCTCTACAAAAATACAAAAGTTAGCCGGGCATGATGGCGGGTGCCTGTAATC T C FRRS1L Ensembl:ENSG00000260230 Protein coding intron GSE47997 K562 cells&HepG2 cells chr9:109160959..109160960 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 RECA 1 - 54958 RMVar_ID_54958 Human_SNP_ID_878204748 A-to-I Human chr9 + 69075754 69075754 69075754 AACTTTTTTTTCCCCTTTCTATTTTTTGAGACAGGATCTCACTTTGGCACTCAGGCTGGAGGACA AACTTTTTTTTCCCCTTTCTATTTTTTGAGACGGGATCTCACTTTGGCACTCAGGCTGGAGGACA A G AL358113.1,FXN Ensembl:ENSG00000285130,Ensembl:ENSG00000165060 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line chr9:69075753..69075754 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_RBP_ID_8705773 RMVar_hsa_circ_257025 54959 RMVar_ID_54959 Human_SNP_ID_878217397 A-to-I Human chr9 - 86375265 86375265 86375265 GAATCCTCAAACTTTTCAATCTCTCTAAAGAAAATGATGTCCACCAGTATGTTGTAAGAAAGCCC GAATCCTCAAACTTTTCAATCTCTCTAAAGAAGATGATGTCCACCAGTATGTTGTAAGAAAGCCC T C AL353678.1 Ensembl:ENSG00000214908 Pseudogene exon GSE100210 HepG2 cell line chr9:86375264..86375265 29129909 RNA-Seq:(High) rs879012957 Functional Loss SNV ICGC 33..33 33 LAML 1 - 54960 RMVar_ID_54960 Human_SNP_ID_878288525 A-to-I Human chr9 - 33676404 33676404 33676404 TGAAAGACATTATGACACCGCCAAATCTAATTACAGAGTTGCGCAATATCCTTTTGAAGACCATA TGAAAGACATTATGACACCGCCAAATCTAATTGCAGAGTTGCGCAATATCCTTTTGAAGACCATA T C PTENP1 Ensembl:ENSG00000237984 Pseudogene exon GSE100210 HepG2 cell line chr9:33676403..33676404 29129909 RNA-Seq:(High) rs1166729043 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_5634448,Human_RBP_ID_22411910 RMVar_hsa_circ_265675 54961 RMVar_ID_54961 Human_SNP_ID_878333270 A-to-I Human chr9 - 70671922 70671922 70671922 CTACTTAAAAAAAAAAAAAAAAAATTAGCTGGACATGGTGGCACATGCCTGTAATCCCAGCTACT CTACTTAAAAAAAAAAAAAAAAAATTAGCTGGGCATGGTGGCACATGCCTGTAATCCCAGCTACT T C TRPM3 Ensembl:ENSG00000083067 Protein coding intron GSE100210 HepG2 cell line chr9:70671921..70671922 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 PRAD,prostate adenocarcinoma 11 prostate RMVar_hsa_circ_6978,RMVar_hsa_circ_27996 54962 RMVar_ID_54962 Human_SNP_ID_878359360 A-to-I Human chr9 - 129944885 129944885 129944885 GTAAGTCATTTAATAAGGTATTTTAATTTTCAATGATAGTAAATGGCCTAGCCCATGGCTAAGAG GTAAGTCATTTAATAAGGTATTTTAATTTTCAGTGATAGTAAATGGCCTAGCCCATGGCTAAGAG T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells chr9:129944884..129944885 24183664 RNA-Seq:(High) rs7870884 Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 4 liver GWAS_ID_6079,GWAS_ID_6080,GWAS_ID_6081,GWAS_ID_6082,GWAS_ID_6083,GWAS_ID_6084,GWAS_ID_6085,GWAS_ID_6086,GWAS_ID_6087,GWAS_ID_6088 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 54963 RMVar_ID_54963 Human_SNP_ID_878433347 A-to-I Human chr9 + 71589582 71589582 71589582 CATCTTGGCTCCTGTGGAGGCCTGCTGGGAACAGGACTTCTAAAAGGAACTATATCTGGAAGGCT CATCTTGGCTCCTGTGGAGGCCTGCTGGGAACGGGACTTCTAAAAGGAACTATATCTGGAAGGCT A G - - Other Unknown GSE100210 HepG2 cell line chr9:71589581..71589582 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_5030958,Human_RBP_ID_17716712,Human_RBP_ID_26566803 54964 RMVar_ID_54964 Human_SNP_ID_878491336 A-to-I Human chr9 + 129809392 129809391 129809392 GACTGATCGACAAAAACCTCATTGATTACTTTATCCCCTTCCTGCCTTTGGAGTACAGACATGTG GACTGATCGACAAAAACCTCATTGATTACTTT_TCCCCTTCCTGCCTTTGGAGTACAGACATGTG TA T TOR1B Ensembl:ENSG00000136816 Protein coding CDS GSE56152 embryonic stem cells,wild type chr9:129809391..129809392 25708366 RNA-Seq:(High) - Functional Loss DEL ICGC 33..33 33 THCA 1 - Human_RBP_ID_8157521,Human_RBP_ID_8925850,Human_RBP_ID_9314428,Human_RBP_ID_22776573,Human_RBP_ID_27131461 Human_Splice_Rec_1089910 Human_miRNA_ID_870611,Human_miRNA_ID_2063113,Human_miRNA_ID_2384507,Human_miRNA_ID_2900779 RMVar_hsa_circ_98530,RMVar_hsa_circ_109271,RMVar_hsa_circ_260248,RMVar_hsa_circ_260249,RMVar_hsa_circ_115176,RMVar_hsa_circ_260252 54965 RMVar_ID_54965 Human_SNP_ID_878506528 A-to-I Human chr9 + 35763717 35763717 35763717 CAGCCTGGCCAACATGGCGAAACCCTGTCTCTACTAAAAATACAAAAATTAGCCGAGTGTGGTGG CAGCCTGGCCAACATGGCGAAACCCTGTCTCTGCTAAAAATACAAAAATTAGCCGAGTGTGGTGG A G - - Other Unknown GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr9:35763716..35763717 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 54966 RMVar_ID_54966 Human_SNP_ID_878506614 A-to-I Human chr9 + 32552446 32552446 32552446 GACTGCTGCCGCCTCCTTACCATGAAGCCAGTAAGTCGTCGCACGCTGGACTGGATTTATTCAGT GACTGCTGCCGCCTCCTTACCATGAAGCCAGTGAGTCGTCGCACGCTGGACTGGATTTATTCAGT A G SMIM27 Ensembl:ENSG00000235453 Protein coding CDS GSE100210 HepG2 cell line chr9:32552445..32552446 29129909 RNA-Seq:(High) - Functional Loss SNV TCGA 33..33 33 LGG 1 - Human_RBP_ID_717396 Human_Splice_Rec_1037279,Human_Splice_Rec_1037283,Human_Splice_Rec_1037285,Human_Splice_Rec_1037287 54967 RMVar_ID_54967 Human_SNP_ID_878534356 A-to-I Human chr9 + 129505281 129505281 129505281 GCCCCTCACCGGAAAGAGAAGCAGGGGGGAGCAGAGGGAGCTTGCAGCCCCACACGCAGGGCTGC GCCCCTCACCGGAAAGAGAAGCAGGGGGGAGCTGAGGGAGCTTGCAGCCCCACACGCAGGGCTGC A T LINC00963 Ensembl:ENSG00000204054 lincRNA intron GSE100210 HepG2 cell line chr9:129505280..129505281 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_miRNA_ID_3206351 54968 RMVar_ID_54968 Human_SNP_ID_878608634 A-to-I Human chr9 + 33038196 33038196 33038196 TGGGCTTTTTAGTAGAGATGGGGTTTCACCATATTGGCCAGGCTGGTCTCAAACTCTTGACCTCA TGGGCTTTTTAGTAGAGATGGGGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTCTTGACCTCA A G DNAJA1 Ensembl:ENSG00000086061 Protein coding intron GSE38233;GSE100210 cultured B-cells;HepG2 cell line chr9:33038195..33038196 24183664,29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 prostate adenocarcinoma 1 prostate 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_256310 54969 RMVar_ID_54969 Human_SNP_ID_878669276 A-to-I Human chr9 - 128305763 128305763 128305763 ATCGCTTGAACCTAGCAAGTCAAGGCGGCAGTAAATGGAGATCTGTACTCCAGCCTGGGCAACAG ATCGCTTGAACCTAGCAAGTCAAGGCGGCAGTGAATGGAGATCTGTACTCCAGCCTGGGCAACAG T C TRUB2 Ensembl:ENSG00000167112 Protein coding 3'UTR GSE38233 cultured B-cells chr9:128305762..128305763 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 BRCA,breast ductal_carcinoma 2 breast Human_RBP_ID_16583356 54970 RMVar_ID_54970 Human_SNP_ID_878688823 A-to-I Human chr9 + 129808832 129808832 129808832 CCTCGGCCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCACACCCAGCAGACACAGAAGTCT CCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCACACCCAGCAGACACAGAAGTCT A G TOR1B Ensembl:ENSG00000136816 Protein coding intron GSE38233 cultured B-cells chr9:129808831..129808832 24183664 RNA-Seq:(High) rs1466038114 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 2 haematopoietic and lymphoid tissue RMVar_hsa_circ_98530,RMVar_hsa_circ_109271,RMVar_hsa_circ_260248,RMVar_hsa_circ_260249,RMVar_hsa_circ_314055,RMVar_hsa_circ_260251 54971 RMVar_ID_54971 Human_SNP_ID_878718015 A-to-I Human chr9 - 83938913 83938913 83938913 GAGACCCCCATCTCTACAAAAATTTAAAAATTAGCCTAGCATGGTGGCACGCTCTGTAATCCCAA GAGACCCCCATCTCTACAAAAATTTAAAAATTTGCCTAGCATGGTGGCACGCTCTGTAATCCCAA T A C9orf64 Ensembl:ENSG00000165118 Protein coding 3'UTR GSE100210 HepG2 cell line chr9:83938912..83938913 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_7940893 54972 RMVar_ID_54972 Human_SNP_ID_878805672 A-to-I Human chr9 + 63819626 63819626 63819626 AATGTCCTTAATAGCAATCCTTAAATGCCATTAAGGACATTTGTGATTGATGGGAGGAGGATGAA AATGTCCTTAATAGCAATCCTTAAATGCCATTGAGGACATTTGTGATTGATGGGAGGAGGATGAA A G MIR4477B Ensembl:ENSG00000266017 miRNA exon GSE126723:GSM3611830,GSM3611831,GSM3611832 Bronchiolar epithelium,BERP35T1 cell line chr9:63819626..63819627 31158229 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_5271687,Human_RBP_ID_17439166 54973 RMVar_ID_54973 Human_SNP_ID_878870980 A-to-I Human chr9 - 125585580 125585580 125585580 ACCTGATCGGGCTCATCTGCTGGCAGTATACAAGCGAAGGACGGGAGCCGAAGCTCAAGTAATCC ACCTGATCGGGCTCATCTGCTGGCAGTATACAGGCGAAGGACGGGAGCCGAAGCTCAAGTAATCC T C MAPKAP1 Ensembl:ENSG00000119487 Protein coding CDS GSE112787 293 Flip-In T-REx cells,empty vector chr9:125585579..125585580 29967493 RNA-Seq:(High) rs781541256 Functional Loss SNV TCGA 33..33 33 ESCA 1 - Human_RBP_ID_5633621,Human_RBP_ID_9408538,Human_RBP_ID_18129660,Human_RBP_ID_27783103 Human_Splice_Rec_1080669,Human_Splice_Rec_1080687,Human_Splice_Rec_1080709,Human_Splice_Rec_1080729,Human_Splice_Rec_1080749,Human_Splice_Rec_1080767,Human_Splice_Rec_1080793,Human_Splice_Rec_1080827,Human_Splice_Rec_1080839,Human_Splice_Rec_1080853,Human_Splice_Rec_1080863,Human_Splice_Rec_1080867,Human_Splice_Rec_1080873,Human_Splice_Rec_1080879 Human_miRNA_ID_1967203,Human_miRNA_ID_1967204 RMVar_hsa_circ_6923,RMVar_hsa_circ_98768,RMVar_hsa_circ_259621,RMVar_hsa_circ_326603,RMVar_hsa_circ_74177,RMVar_hsa_circ_50116,RMVar_hsa_circ_82712,RMVar_hsa_circ_259628,RMVar_hsa_circ_347293,RMVar_hsa_circ_8718,RMVar_hsa_circ_298638,RMVar_hsa_circ_311986,RMVar_hsa_circ_259632,RMVar_hsa_circ_3770,RMVar_hsa_circ_326246,RMVar_hsa_circ_309026,RMVar_hsa_circ_259635,RMVar_hsa_circ_259636,RMVar_hsa_circ_305703,RMVar_hsa_circ_375841,RMVar_hsa_circ_259637 54974 RMVar_ID_54974 Human_SNP_ID_878878302 A-to-I Human chr9 - 33120025 33119979 33120026 CACTTGCCACCATGCGCAGCTAATTTTTGTATATTTTGTAGAGATGGGGTTTTGCTGTATTGCCC CACTTGCCACCATGCGCAGCTAATTTTTGTA__________________________________ TTCGAGACCAGACTGGGCAATACAGCAAAACCCCATCTCTACAAAATA T B4GALT1 Ensembl:ENSG00000086062 Protein coding intron GSE47997 K562 cells&HepG2 cells chr9:33120024..33120025 23474544 RNA-Seq:(High) - Functional Loss DEL ICGC 32..65 33 OV 1 - RMVar_hsa_circ_113644,RMVar_hsa_circ_97414,RMVar_hsa_circ_91506,RMVar_hsa_circ_256330,RMVar_hsa_circ_256331,RMVar_hsa_circ_256332,RMVar_hsa_circ_256333,RMVar_hsa_circ_319028 54975 RMVar_ID_54975 Human_SNP_ID_878900174 A-to-I Human chr9 + 33624860 33624860 33624860 CATTGATTATGAACTGATTGACCAAGATGCCCAGGATCTCTATGACGCTGGAGTGAAGAGGAAAG CATTGATTATGAACTGATTGACCAAGATGCCCGGGATCTCTATGACGCTGGAGTGAAGAGGAAAG A G ANXA2P2 Ensembl:ENSG00000231991 Pseudogene exon GSE100210 HepG2 cell line chr9:33624859..33624860 29129909 RNA-Seq:(High) rs758587386 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_miRNA_ID_1826107,Human_miRNA_ID_1866670,Human_miRNA_ID_1866950,Human_miRNA_ID_1904539 54976 RMVar_ID_54976 Human_SNP_ID_878921176 A-to-I Human chr9 - 110495292 110495292 110495292 AGTCGTGTCTGCTAAGTCCCTTTTACCATGTAAGGCAACGTGTTCACAGGTTCCAGGGATTAGAA AGTCGTGTCTGCTAAGTCCCTTTTACCATGTAGGGCAACGTGTTCACAGGTTCCAGGGATTAGAA T C SVEP1 Ensembl:ENSG00000165124 Protein coding intron GSE100210 HepG2 cell line chr9:110495291..110495292 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_29087,RMVar_hsa_circ_55630,RMVar_hsa_circ_54431,RMVar_hsa_circ_12583,RMVar_hsa_circ_349475,RMVar_hsa_circ_34394,RMVar_hsa_circ_59211,RMVar_hsa_circ_258628 54977 RMVar_ID_54977 Human_SNP_ID_878937687 A-to-I Human chr9 + 128939875 128939875 128939875 CAGGGTTTCACCATGTTGGCCAGGCTGGTCTCAAATTCCTGACCTCAGGTGATCCACCCGCCTTG CAGGGTTTCACCATGTTGGCCAGGCTGGTCTCGAATTCCTGACCTCAGGTGATCCACCCGCCTTG A G PHYHD1 Ensembl:ENSG00000175287 Protein coding intron GSE47997 K562 cells&HepG2 cells chr9:128939874..128939875 23474544 RNA-Seq:(High) rs113073633 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 54978 RMVar_ID_54978 Human_SNP_ID_878969014 A-to-I Human chr9 - 83808348 83808348 83808348 CCAGTGACCTGCCCACCTCGGCCTCCCAAAGTACTGGGATTACAGGTGTGAGCCACTGCACCCGG CCAGTGACCTGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACTGCACCCGG T C GKAP1 Ensembl:ENSG00000165113 Protein coding intron GSE100210 HepG2 cell line chr9:83808347..83808348 29129909 RNA-Seq:(High) rs1226721868 Functional Loss SNV ICGC 33..33 33 MELA 1 - RMVar_hsa_circ_59099 54979 RMVar_ID_54979 Human_SNP_ID_878969063 A-to-I Human chr9 - 129951336 129951336 129951336 TCATCCTAGCACTTTGGGAGGCTGAGGCAGGAAGAGTGCTGGAGGCTAGGAGTTCAAGACCAGCC TCATCCTAGCACTTTGGGAGGCTGAGGCAGGAGGAGTGCTGGAGGCTAGGAGTTCAAGACCAGCC T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells chr9:129951335..129951336 24183664 RNA-Seq:(High) rs10739767 Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 4 liver Human_RBP_ID_1118316 GWAS_ID_6106,GWAS_ID_6107,GWAS_ID_6108,GWAS_ID_6109,GWAS_ID_6110,GWAS_ID_6111,GWAS_ID_6112,GWAS_ID_6113,GWAS_ID_6114,GWAS_ID_6115,GWAS_ID_6116,GWAS_ID_6117,GWAS_ID_6118,GWAS_ID_6119,GWAS_ID_6120,GWAS_ID_6121,GWAS_ID_6122 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 54980 RMVar_ID_54980 Human_SNP_ID_879015161 A-to-I Human chr9 - 93676716 93676716 93676716 GTGGAGGCCGGGGTGGTGGAGGCCGGGGTGGTAGAGGCTGGCGTGGTGGAGGTGGAGGTGGTGCC GTGGAGGCCGGGGTGGTGGAGGCCGGGGTGGTGGAGGCTGGCGTGGTGGAGGTGGAGGTGGTGCC T C - - Other Unknown GSE38233 cultured B-cells chr9:93676715..93676716 24183664 RNA-Seq:(High) rs10821201 Functional Loss SNV ICGC,COSMIC 33..33 33 lung squamous_cell_carcinoma,PRAD,brain oligoastrocytoma_Grade_II,thyroid neoplasm,bile_duct adenocarcinoma,biliary_tract adenocarcinoma,central_nervous_system astrocytoma_Grade_IV,mouth squamous_cell_carcinoma,brain astrocytoma_Grade_IV,central_nervous_system oligoastrocytoma_Grade_II 37 lung,biliary tract,gallbladder,head and neck,brain 54981 RMVar_ID_54981 Human_SNP_ID_879032618 A-to-I Human chr9 - 129948232 129948232 129948232 CTCTCCCTTTGTTGCTCAGGCTGGAGTGCAGTAGTGTGATCAAAACTTATTGCAGCCTCAACCTC CTCTCCCTTTGTTGCTCAGGCTGGAGTGCAGTGGTGTGATCAAAACTTATTGCAGCCTCAACCTC T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells chr9:129948231..129948232 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 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 54982 RMVar_ID_54982 Human_SNP_ID_879038468 A-to-I Human chr9 - 97691536 97691536 97691536 TGACACCTGGCTAATTTTTGGATTTTTTTTGTAGAGACAGGGCTTTGCCATGTTGACCAGGCTGG TGACACCTGGCTAATTTTTGGATTTTTTTTGTGGAGACAGGGCTTTGCCATGTTGACCAGGCTGG T C XPA Ensembl:ENSG00000136936 Protein coding intron GSE38233 cultured B-cells chr9:97691535..97691536 24183664 RNA-Seq:(High) rs1047074213 Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_16519144 RMVar_hsa_circ_258151,RMVar_hsa_circ_350887,RMVar_hsa_circ_327705,RMVar_hsa_circ_258152 54983 RMVar_ID_54983 Human_SNP_ID_879074098 A-to-I Human chr9 + 40326321 40326321 40326321 AGACCCAAGCCTGCCTTGCTGCCACTTAGGATATGACAGCACAGCCAGTGGCCTCTACTGGATCC AGACCCAAGCCTGCCTTGCTGCCACTTAGGATGTGACAGCACAGCCAGTGGCCTCTACTGGATCC A G BX664727.3,FAM95B1 Ensembl:ENSG00000240240,Ensembl:ENSG00000223839 lincRNA,Pseudogene intron,exon GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr9:40326320..40326321 30559470 RNA-Seq:(High) rs1284795417 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_Splice_Rec_1045800,Human_Splice_Rec_1045838,Human_Splice_Rec_1045844,Human_Splice_Rec_1045848,Human_Splice_Rec_1045852,Human_Splice_Rec_1045858 54984 RMVar_ID_54984 Human_SNP_ID_879138973 A-to-I Human chr9 + 134144569 134144569 134144569 TCATAAAAAAACACAAAAACAGGTTGGGTGCCATGTCTCCCACCTGTAATTCCAGCACTTTGGGT TCATAAAAAAACACAAAAACAGGTTGGGTGCCGTGTCTCCCACCTGTAATTCCAGCACTTTGGGT A G WDR5 Ensembl:ENSG00000196363 Protein coding intron GSE38233 cultured B-cells chr9:134144568..134144569 24183664 RNA-Seq:(High) rs4130591 Functional Loss SNV ICGC 33..33 33 LAML 1 - Human_RBP_ID_16612770 RMVar_hsa_circ_7484,RMVar_hsa_circ_47471,RMVar_hsa_circ_310348,RMVar_hsa_circ_274086,RMVar_hsa_circ_9170,RMVar_hsa_circ_104421,RMVar_hsa_circ_303693,RMVar_hsa_circ_260704,RMVar_hsa_circ_260707,RMVar_hsa_circ_80073,RMVar_hsa_circ_260706 54985 RMVar_ID_54985 Human_SNP_ID_879144854 A-to-I Human chr9 + 128631097 128631097 128631097 GAACTCCTGATCTCCAGTGATCTGTCCACCTCAGCCTCCCAAAGTGCTGGGATTACAAGCATGAG GAACTCCTGATCTCCAGTGATCTGTCCACCTCGGCCTCCCAAAGTGCTGGGATTACAAGCATGAG A G SPTAN1 Ensembl:ENSG00000197694 Protein coding intron GSE38233 cultured B-cells chr9:128631096..128631097 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - 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_90080,RMVar_hsa_circ_260041,RMVar_hsa_circ_79030,RMVar_hsa_circ_260042,RMVar_hsa_circ_111172,RMVar_hsa_circ_260044,RMVar_hsa_circ_260045 54986 RMVar_ID_54986 Human_SNP_ID_879154185 A-to-I Human chr9 - 29825554 29825554 29825554 TCTTATTCCTTGGAGCAGGAGAGATTACTCTTAGAATTGCAAATCTTGTAGTATGTCTATGGTAG TCTTATTCCTTGGAGCAGGAGAGATTACTCTTGGAATTGCAAATCTTGTAGTATGTCTATGGTAG T C ME2P1 Ensembl:ENSG00000230097 Pseudogene exon GSE100210 HepG2 cell line chr9:29825553..29825554 29129909 RNA-Seq:(High) rs1383418432 Functional Loss SNV ICGC 33..33 33 LUSC 1 - 54987 RMVar_ID_54987 Human_SNP_ID_879157826 A-to-I Human chr9 - 85935578 85935578 85935578 AGGGCAACCGATTTCTCAGTTTTCACAAACAGAAGTTTCACGCTCTCCCACTTCTCTGGCAATTT AGGGCAACCGATTTCTCAGTTTTCACAAACAGGAGTTTCACGCTCTCCCACTTCTCTGGCAATTT T C RF00017-4706,lnc-GOLM1-4 RNACentral:URS0000954994,RNACentral:URS0000D5B322 SRP RNA,lincRNA intron,intron GSE100210 HepG2 cell line chr9:85935577..85935578 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LAML 1 - 54988 RMVar_ID_54988 Human_SNP_ID_879223795 A-to-I Human chr9 + 118083356 118083356 118083356 ATCTTCTAGATGTCGGAGAACATCTCATTGTGACTGATGAGGTCCTGGTAGATAATCATGATGGC ATCTTCTAGATGTCGGAGAACATCTCATTGTGGCTGATGAGGTCCTGGTAGATAATCATGATGGC A G - - Other Unknown GSE100210 HepG2 cell line chr9:118083355..118083356 29129909 RNA-Seq:(High) rs878970859 Functional Loss SNV ICGC 33..33 33 LAML 1 - 54989 RMVar_ID_54989 Human_SNP_ID_879240886 A-to-I Human chr9 - 89178297 89178297 89178297 TCCCTACTTGGTGTCCGGCGAGGCGCTGCGCAAGGCGCCCGACGATGGGCCCGGCAGCCTGGGCC TCCCTACTTGGTGTCCGGCGAGGCGCTGCGCATGGCGCCCGACGATGGGCCCGGCAGCCTGGGCC T A SHC3 Ensembl:ENSG00000148082 Protein coding CDS GSE107867 ASD brains,frontal_cortex chr9:89178296..89178297 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 THCA 1 - 54990 RMVar_ID_54990 Human_SNP_ID_879243372 A-to-I Human chr9 - 28109061 28109061 28109061 TATGTTGAACCAGCCTTGTATACCAGAGATGAAGCTGACTTGATCGTGGTGGATAAGCTTTTTGA TATGTTGAACCAGCCTTGTATACCAGAGATGACGCTGACTTGATCGTGGTGGATAAGCTTTTTGA T G LINGO2 Ensembl:ENSG00000174482 Protein coding intron GSE107867 ASD brains,frontal_cortex chr9:28109060..28109061 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 54991 RMVar_ID_54991 Human_SNP_ID_879255753 A-to-I Human chr9 + 129506678 129506678 129506678 GCCACCTCGCCCGTCTAATTTTTTGTATTTTTAGTAGAGGCGGGGCTTCACCGTGTTAGCCAGGA GCCACCTCGCCCGTCTAATTTTTTGTATTTTTGGTAGAGGCGGGGCTTCACCGTGTTAGCCAGGA A G LINC00963 Ensembl:ENSG00000204054 lincRNA intron GSE100210 HepG2 cell line chr9:129506677..129506678 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - 54992 RMVar_ID_54992 Human_SNP_ID_879255912 A-to-I Human chr9 - 109135536 109135536 109135536 TGAGGCACGAGAATCACTTGAACCTTGGAGGCAGAGCTTGCAGTGAGCCAAAATTGTGCCACTTG TGAGGCACGAGAATCACTTGAACCTTGGAGGCTGAGCTTGCAGTGAGCCAAAATTGTGCCACTTG T A FRRS1L Ensembl:ENSG00000260230 Protein coding 3'UTR GSE107867 ASD brains,Fragile X samples from NIH NeuroBioBank chr9:109135535..109135536 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 54993 RMVar_ID_54993 Human_SNP_ID_879315359 A-to-I Human chr9 - 19090638 19090638 19090638 GATTCTATGGCTGGGCGAGGTGGCTCACGCCTATAATCCCAGCACTTTGGGAGGTCAGGGCGGGC GATTCTATGGCTGGGCGAGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGTCAGGGCGGGC T C HAUS6 Ensembl:ENSG00000147874 Protein coding intron GSE100210 HepG2 cell line chr9:19090637..19090638 29129909 RNA-Seq:(High) rs571867655 Functional Loss SNV ICGC 33..33 33 LUSC 1 - Human_RBP_ID_26215171 RMVar_hsa_circ_300056,RMVar_hsa_circ_50374,RMVar_hsa_circ_314919,RMVar_hsa_circ_286618,RMVar_hsa_circ_255918,RMVar_hsa_circ_112509,RMVar_hsa_circ_284016,RMVar_hsa_circ_333058,RMVar_hsa_circ_255922,RMVar_hsa_circ_255923,RMVar_hsa_circ_282415,RMVar_hsa_circ_27289,RMVar_hsa_circ_255924,RMVar_hsa_circ_342562,RMVar_hsa_circ_331894,RMVar_hsa_circ_275458,RMVar_hsa_circ_355702,RMVar_hsa_circ_255929,RMVar_hsa_circ_288144,RMVar_hsa_circ_90936,RMVar_hsa_circ_336397,RMVar_hsa_circ_255926,RMVar_hsa_circ_273314 54994 RMVar_ID_54994 Human_SNP_ID_879321715 A-to-I Human chr9 - 37885554 37885554 37885554 AAACCCCATCTCTACTAAAAATACAAAAAATTAGCCAGGCGTGGTGGCGGGCGCCTGTAGTCCTA AAACCCCATCTCTACTAAAAATACAAAAAATTGGCCAGGCGTGGTGGCGGGCGCCTGTAGTCCTA T C AL138752.2,SLC25A51 Ensembl:ENSG00000255872,Ensembl:ENSG00000122696 Protein coding,Protein coding intron,intron GSE38233;GSE126723:GSM3611827,GSM3611828,GSM3611829 cultured B-cells;Bronchiolar epithelium,BEP2D cell line chr9:37885553..37885554 24183664,31158229 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 OV 1 - RMVar_hsa_circ_25731,RMVar_hsa_circ_87790,RMVar_hsa_circ_123415,RMVar_hsa_circ_256954,RMVar_hsa_circ_125064,RMVar_hsa_circ_256955,RMVar_hsa_circ_256956 54995 RMVar_ID_54995 Human_SNP_ID_879337188 A-to-I Human chr9 + 112652751 112652751 112652751 AAGTGATCCACCCTCCTCAGCCTTCTGAGAGTAGCTGGGACTACAGATGTACACCACCATGCCTG AAGTGATCCACCCTCCTCAGCCTTCTGAGAGTGGCTGGGACTACAGATGTACACCACCATGCCTG A G KIAA1958 Ensembl:ENSG00000165185 Protein coding intron GSE100210 HepG2 cell line chr9:112652750..112652751 29129909 RNA-Seq:(High) rs1338208716 Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_258854,RMVar_hsa_circ_258855 54996 RMVar_ID_54996 Human_SNP_ID_879399863 A-to-I Human chr9 - 129927505 129927505 129927505 CAGCCTAACATGTCTAGCAATTTATAAAATAAATGTACAGCTGGGTAATATGGAGGCTCCGTGTA CAGCCTAACATGTCTAGCAATTTATAAAATAAGTGTACAGCTGGGTAATATGGAGGCTCCGTGTA T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells chr9:129927504..129927505 24183664 RNA-Seq:(High) rs4837430 Functional Loss SNV COSMIC 33..33 33 liver hepatocellular_carcinoma 4 liver GWAS_ID_6005,GWAS_ID_6006,GWAS_ID_6007,GWAS_ID_6008,GWAS_ID_6009,GWAS_ID_6010,GWAS_ID_6011,GWAS_ID_6012,GWAS_ID_6013,GWAS_ID_6014,GWAS_ID_6015,GWAS_ID_6016,GWAS_ID_6017,GWAS_ID_6018,GWAS_ID_6019,GWAS_ID_6020,GWAS_ID_6021,GWAS_ID_6022,GWAS_ID_6023,GWAS_ID_6024,GWAS_ID_6025,GWAS_ID_6026,GWAS_ID_6027,GWAS_ID_6028,GWAS_ID_6029,GWAS_ID_6030,GWAS_ID_6031,GWAS_ID_6032,GWAS_ID_6033,GWAS_ID_6034,GWAS_ID_6035,GWAS_ID_6036,GWAS_ID_6037,GWAS_ID_6038,GWAS_ID_6039,GWAS_ID_6040,GWAS_ID_6041,GWAS_ID_6042,GWAS_ID_6043,GWAS_ID_6044,GWAS_ID_6045,GWAS_ID_6046,GWAS_ID_6047,GWAS_ID_6048,GWAS_ID_6049,GWAS_ID_6050,GWAS_ID_6051,GWAS_ID_6052,GWAS_ID_6053,GWAS_ID_6054,GWAS_ID_6055,GWAS_ID_6056,GWAS_ID_6057,GWAS_ID_6058,GWAS_ID_6059,GWAS_ID_6060,GWAS_ID_6061,GWAS_ID_6062,GWAS_ID_6063,GWAS_ID_6064,GWAS_ID_6065,GWAS_ID_6066,GWAS_ID_6067,GWAS_ID_6068,GWAS_ID_6069,GWAS_ID_6070,GWAS_ID_6071,GWAS_ID_6072,GWAS_ID_6073,GWAS_ID_6074,GWAS_ID_6075,GWAS_ID_6076,GWAS_ID_6077,GWAS_ID_6078 RMVar_hsa_circ_82132,RMVar_hsa_circ_116881,RMVar_hsa_circ_260269,RMVar_hsa_circ_363513,RMVar_hsa_circ_260272,RMVar_hsa_circ_69780,RMVar_hsa_circ_378645,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_260279,RMVar_hsa_circ_260278,RMVar_hsa_circ_271812,RMVar_hsa_circ_359498,RMVar_hsa_circ_46271,RMVar_hsa_circ_55216,RMVar_hsa_circ_260282,RMVar_hsa_circ_369227,RMVar_hsa_circ_275039,RMVar_hsa_circ_260283,RMVar_hsa_circ_30836 54997 RMVar_ID_54997 Human_SNP_ID_879409246 A-to-I Human chr9 + 40325426 40325426 40325426 CTGGGAAGTGCTTCCAGGGTTTCATATGTGTTATGGAGATGCTTCCTCTCTCCAACCTCACCGTG CTGGGAAGTGCTTCCAGGGTTTCATATGTGTTGTGGAGATGCTTCCTCTCTCCAACCTCACCGTG A G BX664727.3,FAM95B1 Ensembl:ENSG00000240240,Ensembl:ENSG00000223839 lincRNA,Pseudogene intron,intron GSE107867 ASD brains,Fragile X samples from UC Davis FXTAS brain repository chr9:40325425..40325426 30559470 RNA-Seq:(High) rs4925947 Functional Loss SNV ICGC 33..33 33 LAML 1 - 54998 RMVar_ID_54998 Human_SNP_ID_879433855 A-to-I Human chr9 + 129506786 129506786 129506786 CCATAGTGCTGGGATTACAGGCATGAGCCACCACGCCCGGCTGTTTTATTTCTTATAACTGTACA CCATAGTGCTGGGATTACAGGCATGAGCCACCTCGCCCGGCTGTTTTATTTCTTATAACTGTACA A T LINC00963 Ensembl:ENSG00000204054 lincRNA intron GSE100210 HepG2 cell line chr9:129506785..129506786 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - Human_Splice_Rec_1089552 54999 RMVar_ID_54999 Human_SNP_ID_879467454 A-to-I Human chr9 - 8819062 8819062 8819062 TGTTTTTAATTTTGAAAGTTGATCTCTTGTTAAACCATCATTTTCTAGCATTTTATGCCTTTTTC TGTTTTTAATTTTGAAAGTTGATCTCTTGTTACACCATCATTTTCTAGCATTTTATGCCTTTTTC T G PTPRD Ensembl:ENSG00000153707 Protein coding intron GSE107867 ASD brains,frontal_cortex;ASD brains,temporal_cortex chr9:8819061..8819062 30559470 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 SKCA 1 - RMVar_hsa_circ_93621,RMVar_hsa_circ_255671,RMVar_hsa_circ_782,RMVar_hsa_circ_41058,RMVar_hsa_circ_30632,RMVar_hsa_circ_337868,RMVar_hsa_circ_6059,RMVar_hsa_circ_39742 55000 RMVar_ID_55000 Human_SNP_ID_879492201 A-to-I Human chr9 + 33846175 33846175 33846175 AAAATTAGCCAGGTGTGGTGGCACGAGCCTGTAATCCCAACTTCTTGGGAGGCTCAGGCAGGGGA AAAATTAGCCAGGTGTGGTGGCACGAGCCTGTTATCCCAACTTCTTGGGAGGCTCAGGCAGGGGA A T UBE2R2 Ensembl:ENSG00000107341 Protein coding intron GSE38233 cultured B-cells chr9:33846174..33846175;chr9:33846175..33846176 24183664 RNA-Seq:(High) rs1416398004 Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_16658689 55001 RMVar_ID_55001 Human_SNP_ID_879502005 A-to-I Human chr9 + 19027257 19027257 19027257 ACACGACAGACATACTTCCTACCTGTGATTGGATTGGTGGATGTTGAAAAGCTAAAGCCAGGAGA ACACGACAGACATACTTCCTACCTGTGATTGGGTTGGTGGATGTTGAAAAGCTAAAGCCAGGAGA A G AL356000.1 Ensembl:ENSG00000236680 Pseudogene exon GSE100210 HepG2 cell line chr9:19027256..19027257 29129909 RNA-Seq:(High) rs1477872927 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue Human_RBP_ID_5023930 55002 RMVar_ID_55002 Human_SNP_ID_879506964 A-to-I Human chr9 - 92242228 92242228 92242228 GTGTTATTGAAAGCCACACAGAGTTCATATTTACCACCATAAAGGCTCCCTTGAAACCATATCCA GTGTTATTGAAAGCCACACAGAGTTCATATTTGCCACCATAAAGGCTCCCTTGAAACCATATCCA T C IARS1 Ensembl:ENSG00000196305 Protein coding CDS GSE100210 HepG2 cell line chr9:92242227..92242228 29129909 RNA-Seq:(High) - Functional Loss SNV COSMIC 33..33 33 colon adenocarcinoma,large_intestine adenocarcinoma 5 large intestine Human_RBP_ID_91906,Human_RBP_ID_287309,Human_RBP_ID_8929494,Human_RBP_ID_9239107,Human_RBP_ID_17322932,Human_RBP_ID_18139439,Human_RBP_ID_18400151,Human_RBP_ID_18911512,Human_RBP_ID_27138919,Human_RBP_ID_27376779,Human_RBP_ID_27787682 Human_Splice_Rec_1060835,Human_Splice_Rec_1060901,Human_Splice_Rec_1060969,Human_Splice_Rec_1061033,Human_Splice_Rec_1061047,Human_Splice_Rec_1061053,Human_Splice_Rec_1061057 Human_miRNA_ID_1465248 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_88744,RMVar_hsa_circ_46434,RMVar_hsa_circ_95691,RMVar_hsa_circ_257760,RMVar_hsa_circ_257762,RMVar_hsa_circ_257763,RMVar_hsa_circ_257764,RMVar_hsa_circ_257761,RMVar_hsa_circ_71967,RMVar_hsa_circ_372740,RMVar_hsa_circ_41770,RMVar_hsa_circ_77221,RMVar_hsa_circ_29001,RMVar_hsa_circ_41218,RMVar_hsa_circ_70678,RMVar_hsa_circ_52048,RMVar_hsa_circ_257766,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_46188,RMVar_hsa_circ_50727,RMVar_hsa_circ_40256,RMVar_hsa_circ_257772,RMVar_hsa_circ_345438,RMVar_hsa_circ_372127,RMVar_hsa_circ_257770,RMVar_hsa_circ_365044,RMVar_hsa_circ_314649,RMVar_hsa_circ_257774,RMVar_hsa_circ_30506,RMVar_hsa_circ_36929,RMVar_hsa_circ_21654,RMVar_hsa_circ_257775,RMVar_hsa_circ_257773 55003 RMVar_ID_55003 Human_SNP_ID_879516564 A-to-I Human chr9 - 15461708 15461708 15461708 AACATACTTCACTGTCAAACACATAGGCTTATAGGTTTCGTCAGTTTTCCATGTGTAAGATAAAT AACATACTTCACTGTCAAACACATAGGCTTATTGGTTTCGTCAGTTTTCCATGTGTAAGATAAAT T A - - Other Unknown GSE100210 HepG2 cell line chr9:15461707..15461708 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 COCA 1 - 55004 RMVar_ID_55004 Human_SNP_ID_879519182 A-to-I Human chr9 - 35088748 35088748 35088748 TTGGTCCCAGGAGTTCAAGACCAGCCTGTGGAACATAACAAGACCCCGTCTCTACTATTTAAAAA TTGGTCCCAGGAGTTCAAGACCAGCCTGTGGAGCATAACAAGACCCCGTCTCTACTATTTAAAAA T C PIGO Ensembl:ENSG00000165282 Protein coding 3'UTR GSE100210 HepG2 cell line chr9:35088747..35088748 29129909 RNA-Seq:(High) rs1006958875 Functional Loss SNV TCGA 33..33 33 BRCA 1 - Human_RBP_ID_718340,Human_RBP_ID_8704134,Human_RBP_ID_16667999,Human_RBP_ID_26563596 55005 RMVar_ID_55005 Human_SNP_ID_879534355 A-to-I Human chr9 - 128872822 128872822 128872822 GTGATCTGCCTGCCTCGGCCTCCCAAAGTTCTAGGATTACAGGCCTGAGCCACCACGTCTGGCCA GTGATCTGCCTGCCTCGGCCTCCCAAAGTTCTGGGATTACAGGCCTGAGCCACCACGTCTGGCCA T C AL441992.3,KYAT1 Ensembl:ENSG00000286112,Ensembl:ENSG00000171097 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line chr9:128872821..128872822 29129909 RNA-Seq:(High) rs1393688411 Functional Loss SNV ICGC 33..33 33 LUSC 1 - 55006 RMVar_ID_55006 Human_SNP_ID_879554244 A-to-I Human chr9 - 129926154 129926154 129926154 CAGCCTGGCCAACATGGTGAAACCACATCTCTACTAAAAATACAAAAATTAGCTGGGTGTGGTGG CAGCCTGGCCAACATGGTGAAACCACATCTCTGCTAAAAATACAAAAATTAGCTGGGTGTGGTGG T C FNBP1 Ensembl:ENSG00000187239 Protein coding intron GSE38233 cultured B-cells chr9:129926153..129926154 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 ESCA 1 - RMVar_hsa_circ_82132,RMVar_hsa_circ_116881,RMVar_hsa_circ_260269,RMVar_hsa_circ_363513,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_260279,RMVar_hsa_circ_260278,RMVar_hsa_circ_271812,RMVar_hsa_circ_359498,RMVar_hsa_circ_55216,RMVar_hsa_circ_260282,RMVar_hsa_circ_369227 55007 RMVar_ID_55007 Human_SNP_ID_879573705 A-to-I Human chr9 + 15471105 15471105 15471105 CCATCAATGGGGGGAAGGGGGAAATTCAGTCCAATGAGTCTGTATCAAGATCTTCATCTCTTGTT CCATCAATGGGGGGAAGGGGGAAATTCAGTCCTATGAGTCTGTATCAAGATCTTCATCTCTTGTT A T - - Other Unknown GSE100210 HepG2 cell line chr9:15471105..15471106 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 ovary mixed_adenosquamous_carcinoma,OV 6 ovary 55008 RMVar_ID_55008 Human_SNP_ID_879584581 A-to-I Human chr9 + 98015027 98015027 98015027 TGCCTGCCTTGGCCTCCCAAAGTGCTGGGATTATAGGCATGAGCCAGTGGGCCTGACCAGCTCAG TGCCTGCCTTGGCCTCCCAAAGTGCTGGGATTGTAGGCATGAGCCAGTGGGCCTGACCAGCTCAG A G ANP32B Ensembl:ENSG00000136938 Protein coding intron GSE100210 HepG2 cell line chr9:98015026..98015027 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - 55009 RMVar_ID_55009 Human_SNP_ID_879611317 A-to-I Human chr9 + 124331711 124331711 124331711 TGTGTCAGCGCTGCCTTGCCGGGGATCACACCATGCTGTGCTGCGTCTGTGCCCAGGCCTGGCAT TGTGTCAGCGCTGCCTTGCCGGGGATCACACCGTGCTGTGCTGCGTCTGTGCCCAGGCCTGGCAT A G NEK6 Ensembl:ENSG00000119408 Protein coding intron GSE38233 cultured B-cells chr9:124331710..124331711 24183664 RNA-Seq:(High) rs4838163 Functional Loss SNV COSMIC 33..33 33 frontal_lobe astrocytoma_Grade_III,central_nervous_system astrocytoma_Grade_III 8 brain RMVar_hsa_circ_341141,RMVar_hsa_circ_47270,RMVar_hsa_circ_321337,RMVar_hsa_circ_259441,RMVar_hsa_circ_336561,RMVar_hsa_circ_259447,RMVar_hsa_circ_259448,RMVar_hsa_circ_356819,RMVar_hsa_circ_5449,RMVar_hsa_circ_365008,RMVar_hsa_circ_61552 55010 RMVar_ID_55010 Human_SNP_ID_879666622 A-to-I Human chr9 - 38564265 38564265 38564265 TAGAGCTCAAAAATTTGAAAAATTTGCAGCCTAGCCAAGTGGTCAAAAAGGAAAGCTGATTTTCA TAGAGCTCAAAAATTTGAAAAATTTGCAGCCTTGCCAAGTGGTCAAAAAGGAAAGCTGATTTTCA T A AL390726.2,FAM95C Ensembl:ENSG00000272904,Ensembl:ENSG00000283486 lincRNA,Protein coding intron,intron GSE100210 HepG2 cell line chr9:38564264..38564265 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 PAAD 1 - Human_miRNA_ID_2478923 RMVar_hsa_circ_105053,RMVar_hsa_circ_256973 55011 RMVar_ID_55011 Human_SNP_ID_879720529 A-to-I Human chr9 - 127901372 127901372 127901372 TTAGCCAGGCTGGTCTCGAACTCCTGACCTCAAGTGATCCGCCTGCCTCCCCTCCCAAAGTGCTG TTAGCCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCCGCCTGCCTCCCCTCCCAAAGTGCTG T C ST6GALNAC6,AL157935.3 Ensembl:ENSG00000160408,Ensembl:ENSG00000257524 Protein coding,Protein coding intron,intron GSE100210 HepG2 cell line chr9:127901371..127901372 29129909 RNA-Seq:(High) rs917402663 Functional Loss SNV ICGC 33..33 33 ESCA 1 - 55012 RMVar_ID_55012 Human_SNP_ID_879721711 A-to-I Human chr9 + 37266692 37266692 37266692 GCCCAGGAGTTTGAGACCAGCCTAGGCAATATAGCAAGACTCCATCTCTACAAAAAACAGAAAAA GCCCAGGAGTTTGAGACCAGCCTAGGCAATATGGCAAGACTCCATCTCTACAAAAAACAGAAAAA A G ZCCHC7 Ensembl:ENSG00000147905 Protein coding intron GSE47997 K562 cells&HepG2 cells chr9:37266691..37266692 23474544 RNA-Seq:(High) - Functional Loss SNV ICGC,COSMIC 33..33 33 oesophagus adenocarcinoma,ESCA 3 oesophagus 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_99939,RMVar_hsa_circ_20977,RMVar_hsa_circ_256884,RMVar_hsa_circ_256885,RMVar_hsa_circ_356455,RMVar_hsa_circ_256883 55013 RMVar_ID_55013 Human_SNP_ID_879747866 A-to-I Human chr9 - 95408430 95408430 95408430 CTCTGTCACCCAGGCTGGAGTGCAGTGGTATGATCTCTGCTCACTGCAACCTCCACCACCCGTAT CTCTGTCACCCAGGCTGGAGTGCAGTGGTATGGTCTCTGCTCACTGCAACCTCCACCACCCGTAT T C FANCC Ensembl:ENSG00000158169 Protein coding intron GSE100210 HepG2 cell line chr9:95408429..95408430 29129909 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 MALY 1 - 55014 RMVar_ID_55014 Human_SNP_ID_879803397 A-to-I Human chr9 + 98607966 98607966 98607966 ACTGAAGAACTCTGAAGCTGAGCTCCAGCGGCACCATGAGCAAATGAAAAGGAATTTGGAAGCAC ACTGAAGAACTCTGAAGCTGAGCTCCAGCGGCGCCATGAGCAAATGAAAAGGAATTTGGAAGCAC A G SEPTIN7P7 Ensembl:ENSG00000229897 Pseudogene exon GSE100210 HepG2 cell line chr9:98607965..98607966 29129909 RNA-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_18542156,Human_RBP_ID_26559424 55015 RMVar_ID_55015 Human_SNP_ID_879871828 A-to-I Human chr9 - 3504202 3504202 3504202 TATAGTATATAATATAGTATATAATATATATAATATATATAATATATAATATGTATAATATATAA TATAGTATATAATATAGTATATAATATATATATTATATATAATATATAATATGTATAATATATAA T A RFX3 Ensembl:ENSG00000080298 Protein coding intron GSE47997 K562 cells&HepG2 cells chr9:3504201..3504202 23474544 RNA-Seq:(High) rs1200946702 Functional Loss SNV ICGC 33..33 33 SKCA 1 - 55016 RMVar_ID_55016 Human_SNP_ID_879921063 A-to-I Human chr9 - 33990777 33990777 33990777 CAAAAATTCACTGGGTGTGGTGGTGTACGCCTATAACCCCAGCTACTCGGGAGGCTGAGACAGGA CAAAAATTCACTGGGTGTGGTGGTGTACGCCTGTAACCCCAGCTACTCGGGAGGCTGAGACAGGA T C UBAP2 Ensembl:ENSG00000137073 Protein coding intron GSE38233 cultured B-cells chr9:33990776..33990777 24183664 RNA-Seq:(High) - Functional Loss SNV ICGC 33..33 33 LICA 1 - Human_RBP_ID_24523552,Human_RBP_ID_26220806 RMVar_hsa_circ_121448,RMVar_hsa_circ_256408,RMVar_hsa_circ_110369,RMVar_hsa_circ_3151,RMVar_hsa_circ_256411,RMVar_hsa_circ_119005,RMVar_hsa_circ_126475,RMVar_hsa_circ_93999,RMVar_hsa_circ_256420,RMVar_hsa_circ_256421,RMVar_hsa_circ_256419,RMVar_hsa_circ_84253,RMVar_hsa_circ_256423,RMVar_hsa_circ_47856,RMVar_hsa_circ_256450,RMVar_hsa_circ_38224,RMVar_hsa_circ_298663,RMVar_hsa_circ_294493,RMVar_hsa_circ_256447,RMVar_hsa_circ_256448,RMVar_hsa_circ_334323,RMVar_hsa_circ_305118,RMVar_hsa_circ_274043,RMVar_hsa_circ_87464,RMVar_hsa_circ_256452,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_288718,RMVar_hsa_circ_256464,RMVar_hsa_circ_340458,RMVar_hsa_circ_283254,RMVar_hsa_circ_256470,RMVar_hsa_circ_256471,RMVar_hsa_circ_256469,RMVar_hsa_circ_256481,RMVar_hsa_circ_297548,RMVar_hsa_circ_350421,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_256482,RMVar_hsa_circ_372313,RMVar_hsa_circ_279801,RMVar_hsa_circ_256485,RMVar_hsa_circ_256483,RMVar_hsa_circ_292625,RMVar_hsa_circ_337365,RMVar_hsa_circ_256487 55017 RMVar_ID_55017 Human_SNP_ID_879964611 A-to-I Human chr9 + 71589603 71589603 71589603 CTGCTGGGAACAGGACTTCTAAAAGGAACTATATCTGGAAGGCTGTGGTCCAATGCCATTTTTGC CTGCTGGGAACAGGACTTCTAAAAGGAACTATGTCTGGAAGGCTGTGGTCCAATGCCATTTTTGC A G RPL35AP21 Ensembl:ENSG00000229814 Pseudogene exon GSE100210 HepG2 cell line chr9:71589602..71589603 29129909 RNA-Seq:(High) rs559447636 Functional Loss SNV ICGC 33..33 33 LAML 2 - Human_RBP_ID_26564104 Human_miRNA_ID_1827413 55018 RMVar_ID_55018 Human_SNP_ID_880000463 A-to-I Human chr9 + 98607941 98607941 98607941 ATGAAGGTCAAAGAAAAAGTTCAAAACTGAAGAACTCTGAAGCTGAGCTCCAGCGGCACCATGAG ATGAAGGTCAAAGAAAAAGTTCAAAACTGAAGGACTCTGAAGCTGAGCTCCAGCGGCACCATGAG A G SEPTIN7P7 Ensembl:ENSG00000229897 Pseudogene exon GSE100210 HepG2 cell line chr9:98607940..98607941 29129909 RNA-Seq:(High) rs1397022118 Functional Loss SNV ICGC,COSMIC 33..33 33 LAML,haematopoietic_and_lymphoid_tissue acute_myeloid_leukaemia 4 haematopoietic and lymphoid tissue Human_RBP_ID_18542156,Human_RBP_ID_26559423